Zeiss Atlas 995 Manual Dexterity

Posted : admin On 13.08.2019
  1. Zeiss Atlas 995 Manual Dexterity Test

View & download of more than 288 Zeiss PDF user manuals, service manuals, operating guides. Microscope user manuals, operating guides & specifications. I'm in need of a manual for the an early Zeiss/Humphrey Atlas 900 series topographer with the Masterview software. Anyone out there still have one that would be willing to make a copy?

Published online 2013 Jun 18. doi: 10.1186/1471-244X-13-169
PMID: 23773398
This article has been cited by other articles in PMC.

Abstract

Background

Since Goffman’s seminal work on psychiatric institutions, deinstitutionalization has become a leading term in the psychiatric debate. It described the process of closure or downsizing of large psychiatric hospitals and the establishment of alternative services in the community. Yet, there is a lack of clarity on what exactly the concept of institutionalization means in present-day psychiatry. This review aims to identify the meaning of psychiatric institutionalization since the early 1960s to present-day.

Method

A conceptual review of institutionalization in psychiatry was conducted. Thematic analysis was used to synthesize the findings.

Results

Four main themes were identified in conceptualizing institutionalization: bricks and mortar of care institutions; policy and legal frameworks regulating care; clinical responsibility and paternalism in clinician-patient relationships; and patients’ adaptive behavior to institutionalized care.

Conclusions

The concept of institutionalization in psychiatry reflects four distinct themes. All themes have some relevance for the contemporary debate on how psychiatric care should develop and on the role of institutional care in psychiatry.

Keywords: Psychiatric Institutionalization, De-institutionalization, Re-institutionalization, Mental Health Care

Background

In the 19th and early 20th century, asylums were the main form of care for patients with severe mental illness (SMI). Illustrating the problematic effects of asylums, Goffman, coined the term “total institution” from a sociological perspective in his seminal work Asylums[1]. The concept “total institution” refers to the life of psychiatric patients in institutional settings and originated from his ethnographic fieldwork in 1955–6 in a federal institution of over 7,000 inmates in Washington D.C, United States. His objective at the time was to learn about the social world of the hospital inmates by subjectively experiencing their world. He emphasized that mental hospitals were prison-like institutions although the members had not broken the law. Similarly, he defined ‘psychiatric institutions’ as a closed system apart from the rest of society. He claimed that patients received custodial care and typically lived all aspects of their life in a psychiatric hospital with limited access to the outside world. In a total institution, each phase of the patient’s daily activities was carried out in the immediate company of a large number of other people. All activities were tightly scheduled and the series of performed activities was enforced from the top. Patients’ lives were dictated by institutional routine and isolated from the wider society for an extensive period of time. Goffman further described extensively how inmates underwent a mortification of self, through physical and social abuse, which then lead to the loss of their usual identify. This ‘mortification of self’ involved a process whereby the individual was stripped of their past roles to take on a purely institutional role. In essence, Goffman perceived psychiatric hospitals as establishments that shared the same characteristics as prisons, concentration camps and monasteries and argued that patients were subjected to restriction of freedom, suffered from the stigma of being a psychiatric patient and had their normal social roles taken away.

However, deinstitutionalization of psychiatric patients became widespread as a result of several major factors. Besides the upcoming civil rights movement and the right to receive treatment in the least restrictive environment possible, advances in antipsychotic drugs and alternative care in community enabled the release of patients from mental hospitals. Moreover, the high cost of inpatient mental health care became an increasing financial burden for the developing welfare state. The term ‘deinstitutionalization’ described the process of closure or downsizing of large psychiatric hospitals and the establishment of alternative mental health care in the community. Since deinstitutionalization began in the 1950s, the roles of psychiatric hospitals have changed, and more than half a million long-stay patients have been discharged from psychiatric hospitals in the United States and United Kingdom[,]. Psychiatric services in Western countries have moved away from being based on large psychiatric hospitals to community-based care. An extensive body of literature has described de-institutionalization processes, e.g. in Italy[], Norway[], Germany[] and the United Kingdom[]. The effects of deinstitutionalization vary across countries based on their health care and social welfare systems as well as the specific features of national traditions, socio-cultural context, and the level of available resources[8]. Nevertheless, inpatient psychiatric hospital services are still considered an essential type of care in psychiatry today, as community care may not be suitable for all patients, especially those with acute mental illness and a lack of support. Nearly all patients with severe mental illness are treated mostly in the community yet many people still episodically receive standard inpatient hospital care[]. It has been argued that the importance of institutionalized care may be rising again regardless of the investment in community mental health services over the past few decades. Supporting this argument, studies suggest that in several countries the provision of institutional care has increased since 1990[-]. Although the number of traditional psychiatric beds continues to fall in most Western countries, a significant increase in forensic psychiatric beds and places in supported housing services in several industrialized countries across Western Europe has been observed. This has been described as ‘re-institutionalization’, whilst others argue that it is a ‘trans-institutionalization’ with patients who would have been long-term hospitalized before de-institutionalization now ending up in different institutions such as residential homes, forensic hospitals and prisons[].

However, despite the debate on whether the development of mental health care constitutes deinstitutionalization, re-institutionalization or trans-institutionalization, there is little common understanding on how the term ‘institutionalization’ has been conceptualized and understood in the field of psychiatry since the work of Goffman. It is therefore the aim of this paper to review and identify meanings and connotations of institutionalization starting from Goffman’s work on mental hospitals to the present day, focusing mainly within the field of psychiatry and medicine. The objective of this review is not to come up with a new definition but to analyze how the term has been used in the psychiatric literature.

Methods

A conceptual review of institutionalization in psychiatry was conducted. To synthesize concepts of the phenomenon ‘institutionalization’, the principles of conceptual reviews as described by Lilford et al.[] were followed. Unlike a standard systematic review, the aim of a conceptual review is not to review all literature but to search widely using various databases and sources; building in safety nets to minimize potential biases (e.g. multidisciplinary study teams) and incorporating some overlap in the various stages of the review process so that the precise direction of the review can be clarified. For the purpose of this paper, the concept of institutionalization described by Erving Goffman in 1961[1] was selected as the starting point to the diverse and extensive literature because Goffman’s definition of psychiatric hospitals as ‘total institutions’ was influential and still remains strongly in the minds of sociologists, psychiatrists, and service user advocates[].

To commence, electronic searches were performed and the literature known to the authors was also considered. The databases searched were: Pubmed, Web of Science, PsychINFO, and Scopus as they are widely considered as the most relevant databases for publications in the fields of psychology, psychiatry, and other medical disciplines. For each database, searches were performed using the term “institution* AND severe mentally ill*”, seeking for all literature since Goffman’s work on mental institutions from January 1961 to February 2012. This was later supplemented through additional searches using more psychiatric institutionalization specific terms: (psychiatr* institutionalization AND mental illness) and (mental institution* AND psychiatr*). The titles and abstracts of all identified papers were then reviewed for their relevance. To search widely, the reference lists of all identified relevant papers were also examined to uncover new potential references that were not included in the selected databases. Therefore, although the focus of the review is on the field of psychiatry, some papers also tap into other disciplines such as history, law and sociology if there was a direct link to psychiatry found in the papers by the authors. Full papers were read if necessary to determine their significance before discarding. The concepts uncovered from an initial search of the literature guided further more specific searches around those concepts.

Identified articles were eligible for this study if they met at least one of the following two inclusion criteria: A) mentioning the characteristics, experiences, and/or the functions of adult psychiatric institutions and institutionalization, B) reporting the effect of institutionalization. However, only those papers were included that did not meet any of the following two exclusion criteria: First, papers were excluded if studies about psychiatric hospitals were not based in countries that had experienced major mental health care reforms involving deinstitutionalization during the second half of the 20th century. The reason for excluding such papers is because countries that had not undergone the process of deinstitutionalization at the time may operate on a different organization of mental health care system[]. Second, papers were excluded if studies focus mostly on psychiatric reforms or the process of deinstitutionalization. Third, papers were also excluded if institutionalization of older adults, children or intellectually disabled were examined, since the review focused on the concept of institutionalization for the core group of patients of working age.

Thematic analysis, a method used for identifying patterns of meaning, was employed to synthesize the findings[17]. Information on the characteristics and functions of psychiatric institutions was extracted from all identified papers and was then analysed in chronological order. This analytic approach was chosen in order to reflect historical trends in the development of psychiatric services. Analysis was regularly reviewed through weekly meetings between WSC and SP, and findings were then presented to the study team and alternative interpretations discussed, in order to minimize any potential biases. Identified categories were then refined, subsumed within existing categories or deleted. The study team comprised a clinical psychiatrist (SD), a research psychologist (RMcC), a psychiatrist who is both a clinician and an academic (SP), and a public health researcher who is also trained as a mental health clinician (WSC). The team drew on their professional experience in various clinical settings, background knowledge of different countries’ health care systems and familiarity with conducting conceptual reviews. The study group was asked to comment on the preliminary themes, the initial draft of this review and to identify any further relevant literature that was not included. The study team’s expertise was utilized to identify patterns as well as to combine related subject matters through discussions. Findings were then grouped based on the underlying concepts which appeared to guide them. The discussions with the study team provided a validity check on the identified themes.

Results

While this review does not aim for exhaustive searching, a brief summary of the results of the searching protocol is provided as a general understanding of the search process. Figure 1 shows the flow diagram detailing the study retrieval process.

Flow diagram for paper selection.

The initial electronic searches produced 2,110 items, which was reduced to 759 after elimination of duplicates and unrelated items. A further 43 items were added from the examination of reference lists. 177 items remained after the elimination of 625 irrelevant materials. Only papers meeting the inclusion criteria were included in the final review (n = 61).

Overview of papers

Identified publications dated from 1961 to 2012. Data was extracted from 61 papers across eleven Western industrialized countries (Australia, Canada, France, Germany, Italy, Ireland, Netherlands, Sweden, Switzerland, United Kingdom, and United States).

Four main themes were identified. The degree to which these themes have been addressed and specified in the literature varies substantially. They appear to be conceptually distinctive but also to some extent interrelated. The four guiding principles underlying concepts of institutionalization are: a) bricks and mortar of care institutions, b) policy and legal frameworks regulating care, c) clinical responsibility and paternalism in the clinician-patient relationship, and d) patient’s adaptive behavior to institutionalized care. The characteristics of these papers are summarized in Table 1. Each publication sometimes addressed more than one theme.

Table 1

Conceptualization of the termInstitutionalization

Author(s), yearCountryBricks &mortarPolicy &legal frameworksClinical responsibility &paternalismPatients’ adaptive behavior to care
1960s
Pine & Levinson, 1961[75]U.S.AX
Wing & Brown, 1961[67]U.KXX
Wing 1962[63]U.KX
Barton, 1966[69]U.S.AX
Gruenberg 1967[73]U.S.AX
Karmel, 1969[65]U.S.AX
1970s
Gomia et al. 1970[30]U.S.AXXX
Wing & Brown, 1970[64]U.KXX
Moos, 1972[23]U.S.AXX
Ochberg et al., 1972[68]U.S.AX
Moos, 1973[24]U.S.AXX
Rosenhan, 1973[71]U.S.AX
1980s
Johnstone, Owens et al. 1981[74]U.KX
Liberakis, 1981[70]CanadaXX
Goldney, Bowes et al., 1985AustraliaX
Wasow, 1986[48]U.S.AX
Talbott & Glick, 1986[46]U.S.AX
1990s
Myers, Leahy et al., 1990U.KXX
Wing, 1990[49]U.KXX
Curson, et al. 1992[66]U.KX
Abrahamson, 1993U.KX
Taj and Sheehan, 1994[25]IrelandXX
Prior, 1995[51]U.KX
Eklund & Hansson, 1997[47]SwedenX
Breeze, 1998SwedenX
Ford, et al. 1998[72]U.KX
Lutzen, 1998[61]SwedenX
Owen, Tarantello, et al. 1998[52]AustraliaXX
McCubbin & Cohen, 1999[59]UKX
Nijman, a Compo et al., 1999[53]The NetherlandsX
2000s- Present
Boardman & Hodgson, 2000[19]U.KX
Quirk & Lelliott, 2001[56]U.KX
Bowers, Crowhurst et al., 2002[34]U.KX
Dvoski et al., 2002[22]U.S.AX
Lewis, 2002[36]U.KX
Zinkler & Priebe, 2002[39]U.KX
O’Brien & Cole, 2003[50]AustraliaXX
Salize &Dressing, 2004[40]GermanyX
Priebe, 2004[18]U.KX
Rittmannsberger et al., 2004[31]EuropeX
Canvin, Bartlett & Pinfold, 2005[55]U.KX
Karlin & Zeiss, 2006[28]U.S.AX
Katsakou & Priebe, 2006[41]U.KX
Killaspy, 2006[54]U.KX
Quirk, Lelliott & Seale, 2006[20]U.KXXX
De Girolamo et al., 2007ItalyXX
Haglund et al., 2007[33]SwedenX
McNown Johnson & Rhodes, 2007[38]U.S.AXXX
Sine, 2008[26]U.S.AX
Johnson, Gilburt et al. 2009[21]U.KXX
van der Merwe et al. 2009[32]U.KXXX
Priebe, Katsakou et al., 2009[58]U.KXX
Coldefy & Curtis, 2010[29]FranceX
Katsakou, Bowers et al., 2010[42]U.KX
Lang et al., 2010[35]GermanyX
Molodynski, Rugkåsa & Burns, 2010[44]U.KXX
Priebe, Katsakou et al., 2010[43]U.KX
Sheehan & Burns, 2011[57]U.KXX
Lay, Nordt & Roessler,2011[60]SwitzerlandX
Georgieva, Mulder & Wierdsma, 2012[37]The NetherlandsX
Reumschussel-Wienert & Crefeld, 2012[45]GermanyX

Findings revealed the characteristics and experiences of institutionalization and how the concept evolved and different themes emerged chronologically (see Figure 2). Most of the papers from our review, i.e. 43 out of 61, originated from the last twenty years. Papers from the earlier period focus on recognizing institutionalization as patients’ response to institutional care and the impact institutional care has on patients’ self-concept, while the later papers give emphasis to policy and legal frameworks regulating care and clinical responsibility and paternalism in clinician-patient relationships. In summary, the theme clinical responsibility and paternalism in clinical-patient relationships becomes visible only in recent debates about psychiatric institution, while the concept of institutionalization as bricks and mortar of care institutions has been a part of the conceptualization of institutionalization from its beginnings up until the present day.

Prevalence of the four identified themes from 1961–2012.

Bricks and mortar of care institutions

Goffman emphasized how psychiatric hospitals were characterized “by the barrier to social intercourse with the outside and to departure that is often built right into the physical plant, such as locked doors, high walls, barbed wire, cliffs, water, forests or moors”[1,]. Such physical elements of ‘bricks and mortar’ are still defined as a key feature of many conventional institutions such as hospitals and residential care amenities in the literature[]. On the other hand, in a departure from the historical context, the barrier between modern psychiatric in-patient settings and the rest of the world is less clear. Research demonstrates that the expansion of community-based mental health care has reduced the physical boundary and isolation between psychiatric institutions and the outside world[19-]. It was found, for example, that fencing was picked as the preferred material for the outdoor recreation yards rather than solid walls the a forensic psychiatric unit of the Colorado Mental Health Institute[].

Similar to Goffman’s notion, a comparable but slightly different way to grasp the concept of a psychiatric institution is by the architectural design of the building[-]. The structural design of psychiatric hospitals can play a role in the treatment process but also the safety of the doctors[,]. Since the early 19th century, the architectural layout of asylums originated from a belief that cure could not occur unless psychiatric patients were isolated from their familiar home environment and put into a suitable “therapeutic space”. Relatedly the term “architectural paternalism” is currently used and the clinical ethics of the architectural design of psychiatric inpatient facilities have been examined[]. The basis of the ethic of paternalism in the design of psychiatric facilities has also been considered in the context of modern thinking about psychiatric hospitals. Sine argued that the limitation of patients’ rights and autonomy caused by the architectural design of inpatient facilities is legitimate and ethical when it is used to prevent harm and danger[].

In addition to understanding the physical aspects of psychiatric hospitals as a key aspect of institutionalization, the geographical locations of institutions, i.e. remoteness from local community and cities, has been identified as another characteristic of institutional psychiatric care. In France, Coldefy and Curtis[] analyzed the geographical locations of specialized psychiatric hospitals from 1800–2000 with a stronger focus on the earlier period. Limitations of classical models of spatial diffusion, the processes of the conservation and transformation of geographical spatial structures, were found although not consistent with all the different phases of development of psychiatric institutions. The developmental process of these psychiatric hospitals seems to be associated with the national policies, social representations, and medicalization of care of mental illness, urbanization and economic growth. The authors therefore suggested that a political ecology approach, a model that takes into account the relationship between political, economic and social factors with environmental issues and changes, might be more appropriate to understand the vast development of French psychiatric care[].

As Figure 2 reveals, the theme of bricks and mortar has constantly been in part discussed in the literature over the time period covered in this review. However, relatively few papers have focused on this theme prominently compared to others. The narrow focus may have been triggered by the deinstitutionalization movement and the negative perception of the institutions as dehumanizing and damaging for the mentally ill. Despite the negative connotation people have formed about institutions, it appears that mental health professionals have always been concerned about this aspect of mental health care as it is an underlying principle of moral therapy – it defines the physical place where care is provided and where treatment is give to patients and thus has always been part of the debate.

Policy and legal frameworks regulating care

Before the radical shift from large psychiatric hospitals to community-based services, the physical building of large mental hospitals defined institutional care[1]. However after the deinstitutionalization movement, institutional care has also been conceptualized in terms of the policies and legal framework of the relevant institutions and national legislation that limit the patients’ autonomy. Although there has been a tendency to open wards up and allow patients free movement, many psychiatric hospitals still operate to some extent as a safeguarding system, and a considerable amount of care is still provided behind locked doors[30-]. For instance, large numbers of Swedish inpatient psychiatric wards are locked[] and 22 out of 87 acute wards in London were locked permanently according to a study in 2002[]. This occurs despite evidence from a German study that a closed entrance door to an acute psychiatric ward did not reduce absconding[35]. In an ethnographic study of three acute wards in London, Quirk and colleagues found that entrance doors may also be locked temporarily to prevent patients from escaping while some patients might be required to transfer to a locked, intensive care unit[]. On wards that have more of a permeable nature, instead of locking patients up, an alternative method has been employed to manage the risk of patients running away or self-harming – a staff member is appointed to observe the patient closely at all times. Besides placing a patient in a locked care unit, seclusion, restraint and sedation are also identified as interventions to monitor and control the high-risk and potentially dangerous behaviors of a patient who is experiencing a severe psychotic episode[,].

Restriction of freedom is still often associated with psychiatric institutionalization and hospital treatment although modern psychiatric wards and hospitals have been found to be ‘permeable’[]. Similar to Goffman’s interpretation of psychiatric hospitals, McNown Johnson & Rhodes characterized psychiatric institutions as establishments where their residents have little or no choice about their participation in activities, and have little say about how they are being treated[38]. Admitted residents are not allowed to leave the psychiatric institution without being officially released or discharged. From this perspective, patients’ freedom of movement is restricted and the functions of psychiatric institutions are similar to a security guard.

Besides exploring locked facilities as one type of psychiatric treatment model, legislation has also been set up for the practice of involuntary placement or treatment of people with mental illness. The mental health law and legal framework for involuntary placement or treatment varies across Europe. Significant numbers of patients in Europe are involuntarily admitted to psychiatric hospital units[]. Frequencies of compulsory admission were found to vary across the European Union[]. However, law and practice does not always coincide. Katsakou and Priebe[] found that many patients feel retrospectively that the involuntary admission was justified while another study revealed a significant proportion of formally voluntary patients feel coerced[]. The variation across countries might be related to differences in legislation between countries[]. The differences between the legislation and patients’ view of mandatory treatment often lead to question whether admission was right or not. Therefore, it is critical to regulate any psychiatry practice that limits the autonomy of an individual.

Restriction of freedom of choice and social integration of patients with mental illness may also occur in community psychiatric treatment settings. In England and Wales, the Mental Health Act 1983, which was amended in 2007 considerably, allows individuals with a mental disorder to be admitted to hospital, detained or treated against their will for both their own health and safety or for the protection of the general public. Compulsory community treatment was introduced as one of the amendment to the Mental Health Act 1983. Molodynki, Rugkåsa and Burns[] suggest that the Mental Health Act has increased the capacity for compulsion in the community and is reflected in the recent changes in service provision, although the evidence base is relatively small. In Germany, the advantages and disadvantages of closed psychiatric homes in Berlin were discussed recently in a debate paper[]. Reumschuseel-Wienert argued for closed psychiatric homes because community psychiatric facilities are not capable of providing sufficient care for patients with severe limitations, such as a lack of insight into their illness, an inability to regulate or control their emotions, or to structure their time and the organization of their self-care. Crefeld, on the other hand, suggested that it is not unknown that patients with severe mental impairments often need help to cope with everyday life. He claimed that it is difficult to provide person-centered treatment in closed psychiatric homes because this form of care generally offers all residents the same consistent care package regardless of whether the individual residents need it or not.

As the numbers in Figure 2 show, the attention to the theme of policy and legal framework emerged after the year 2000. Before this, little attention was paid to this aspect of institutionalization. This may be because most mentally ill people are no longer treated in large mental hospitals in remote areas as a result of the changing pattern of mental health care – the closure of large mental hospitals, the decline of psychiatric hospital beds, short stay admissions and the development of care in community. Therefore the emphasis has then shifted towards more on the legal aspect, such as the rise of compulsory treatments[].

Clinical responsibility and paternalism in clinician-patient relationships

Institutional care can also be characterised by the service organization and the responsibility that mental health professionals have for patients. Besides safekeeping the patients, many treatment and care elements such as shelter and protection are also provided on modern inpatient hospital wards[]. Inpatient treatment for instance offers the chronic mentally ill patients, whose symptoms cannot be controlled in an outpatient program a structure in which treatment can effectively control their symptoms. For instance, antipsychotic medication has been considered as a primary inpatient treatment modality. It has been seen as helpful and effective in suppressing psychotic symptoms in the hospital, but also as potentially hindering community adaptation on discharge. For this reason, Talbott and Glick argue it is essential to reduce medication at some point after discharge[].

While many mental health professionals perceive psychiatric institutions as a treatment model that is isolating the mentally ill, in the late 1990s, the treatment environment provided by inpatient wards has been considered potentially beneficial for patients[]. Linked to this, psychiatric institutionalization has been seen as providing protection and care to patients who are chronically mentally ill[,-51]. It has been highlighted that even the best community care does not offer enough care and protection for the many chronically mentally ill and the need for sanctuary and asylum can only be provided as an institution of some kind[]. Wasow claimed that institutionalization does not necessarily cause dependency; rather it provides a permanent, structured, supervised housing for the chronically mentally ill[]. In addition, institutional care protects this vulnerable population from the prejudice and the hostility that they might experience in the larger society. Samuel, a typical case of a single patient, who spent 36 years in a large mental hospital in Northern Ireland, was reported as an example of a patient utilizing the hospital as a lodging house. Meanwhile he did odd jobs such as gardening for his fellow churchgoers and went to church regularly in his last ten years[51]. He had been an involuntary patient for the first 25 years of his stay and then refused to be discharged from the institution because he was happy with his life at the time.

However, despite the fact that the main purpose of psychiatric institutions is to provide a stable environment to facilitate the treatment process so that patients’ psychotic symptoms could be reduced, nevertheless patients’ safety and wellbeing are threatened by violence from patients on inpatient psychiatric wards[,]. Nijman and his associates claimed that the hospital’s environment inescapably introduces stressors on the patient. The violent behaviour by patients with psychotic disorders on the wards is exacerbated by some negative forms of environmental and interpersonal stimulation such as the disorganization of a crowded psychiatric ward, noise[], the lack of interesting activities, and/or problematic communication with staff members.

A more recent way to understand institutionalization in psychiatry is in terms of the relationship between staff members and patients. In the present day, psychiatric care does not rely solely on hospital facilities. As a result of the large reduction of psychiatric hospital beds and the re-focus of institutionalized care to community treatment, more people with severe mental illnesses are treated in community-based settings[,]. There are several residential alternatives although they cannot be considered as an optimal option for all patients to acute inpatient psychiatric services[19].

To conceptualize institutionalization purely based on the length of hospital stay within bricks and mortar, locked up hospitals or basing it on the change of patients’ identity and social position prior/after to admission might not reflect the practice of institutionalization in contemporary psychiatric institutions. For example, institutions can be understood as a web of people, ideas and practical/potential power in our contemporary society[]. Moreover, patient-nurse relationships are recognized as an essential aspect of therapeutic psychiatric in-patient care[]. A cross-sectional cohort study of the association between perceived coercion and therapeutic relationship by Sheehan and Burns[] concluded that “hospitalization, even when voluntary, was viewed as more coercive when patients rated their relationship with the admitting clinician negatively”. Moreover, patients’ perception of their treatment engagement matters. Priebe and his team found in an observational prospective study that involuntarily admitted patients with initial satisfaction with treatment were associated with more positive long-term outcomes[]. They concluded it is important for clinicians to consider patients initial views as a relevant indicator for their long-term prognosis of involuntarily admitted patients. Moreover, “institutions do not necessarily have walls”[]. Staff and patients in community treatment teams such as assertive outreach engage in an obligatory close relationship, as the aim of community services is to provide treatment to people who do not seek it themselves. Whether services are being provided on wards or in the community, these intense relations between staff and patients may also define institutionalized care, particularly if the social interaction among members of an institution is mandatory as a result of involuntary admission.

The relationships between the clinical staff and patients as well as among patients themselves are unequal in terms of social power. For instance, on wards very few admitted patients have “privileges” in terms of the allocation of preferred accommodation, access to social facilities, activity, or extra food[30]. Members of staff are required to keep an eye on the admitted patients on a regular basis to ensure patients are not in any danger. Clinical staff, particularly psychiatrists, have authority but also responsibility for patients’ safety[]. Patients’ right to autonomy is nonetheless usually restricted by staff in psychiatric inpatient wards for their wellbeing. It has been found that staff members behave more paternalistically towards patients within highly formalized institutions, but are more in agreement with patients in less formal ward environments[]. Also, depending on the culture of the wards or mental hospitals, patients can either be motivated to speak or made quiet by staff[].

Relatedly, the paternalistic relationships between staff and patients are also shown through the use of coercion. A variety of forms of coercion (informal or formal) is frequently practiced by clinical staff to ensure medication adherence[]. The openness between a clinician and his or her patient/client could change depending on the social culture of the institution such as treatment design and the mental health as well as the legal status of the patient (i.e. voluntary versus involuntary). In a mixed methods study, Katsakou and associates[] identified that roughly one third of the voluntary patients felt coerced into admission and half of them continued to feel coerced into treatment a month later. Patients felt less coerced if their satisfaction with inpatient hospital treatment also increased. Yet the usage of coercion is often justified in mental health settings on the notion that patient’s health condition hinders his or her ability to make a sound decision[,]. Formal coercive treatment outside hospitals such as community treatment orders are also commonly accepted and practiced[].

The theme of clinical responsibility and paternalism emerged in the 1970s but as the numbers in Figure 2 suggest, attention to this theme increased substantially in the 1990s. In this decade, the majority of the identified papers included this theme. This may be explained by the general debate during this time frame on how to best care for patients or serve those service users most in need – the act for balancing the rights of the patients and the responsibilities of the clinical professionals.

Patients’ adaptive behaviour to institutionalized care

Institutionalization in psychiatry can also be characterised by symptoms exhibited by patients in response to being treated in an institution, i.e. the patients’ adaptive behaviour to care. Institutionalism was a term adopted by Wing[63] to describe a trend observed during a study of the long -stay male patients of two large hospitals in 1950s in England, which he later on also termed ‘social withdrawal’[64]. Initially it was recognized as a syndrome in inpatient psychiatric facilities, and is now used to describe a set of maladaptive behaviours that are induced by the tensions of living in any institution[,64-]. Wing and Brown[64] defined institutionalism as the association between the poverty of the physical environment and severity of primary symptoms of the illness and secondary disabilities that are not part of the illness itself, and identified three variables that increase the damaging effect: the social pressures that stem from an institution, the length of time that the resident was exposed to these pressures, and the level of predisposition that the resident brought[63,67].

Wing & Brown[64,67] studied the impact of institutionalized care on patients with severe mental illnesses. The objective was to test the notion that there is an association between the social conditions of psychiatric hospitals and the clinical state of the patients. Wing and Brown found that patients with schizophrenia had fewer negative symptoms when they were treated in hospitals with richer social environments and opportunities. In addition, these patients showed distinctly fewer disturbances in verbal and social behaviour. In contrast, patients with the least social interaction, fewest activities to take part in, and the least access to the outside world were the most unwell.

Patients who reside in any institutional setting such as psychiatric hospitals or prisons are often socially isolated or have limited access to the outside world. In other words, individuals in institutions may lose independence and responsibility, to the point that once they return to life outside of the institution, they are often unable to manage everyday demands. A number of authors preferred the term “institutionalism” for this phenomenon[], while Barton[] argued the term “institutional neurosis” is more adequate to refer to the disability in social and life skills as a result of adaptation to the demands of an institution. He also stated that the term “institutional” does not indicate that institutions are the only cause of such disability, and that the behaviour was only first recognized in institutions. Institutionalism, defined as “the impoverishment of feelings, thoughts, initiative and social activity” may be found among patients in boarding homes and some premorbid features of patients, i.e. low intelligence, poor education and disability in hearing, speech, locomotion and manual dexterity, may make them more susceptible to institutionalism than others[].

Alternatively, depersonalization and the loss of one’s identity have been suggested as key features of institutionalism[1,]. Institutional environments can be perceived as humiliating, and admissions to acute psychiatric wards can be stigmatizing and non-therapeutic[]. Many inpatients upon admission adapt to their environment intrinsically, particularly those who live for prolonged periods in restricted environments. They become dependent on receiving care from services, lose their confidence to make decisions and consequently become institutionalized.

Similarly, Gruenberg linked institutionalization to “social breakdown syndrome” (SBS)[]. SBS can be characterized as the loss of normal role functioning with a varying degree of exclusion from typical family or community roles. The features are similar to the negative symptoms of schizophrenia. SBS can be the by-product of any treatment that removes the patient from his or her regular social environment (i.e. long-term hospitalization or “overprotection” excessively on the part of clinical staff and/or family members). The author claimed that there are seven stages of SBS and compared the last stage, ‘identification with the sick’, with Goffman’s last mode “conversion”. He argued that in such a stage a patient accepts the status of the chronic sick role and identifies with the other sick patients around him.

However, on the other hand, not all long-stay patients are affected negatively by psychiatric institutions. No difference in terms of cognitive deficits was found in a study comparing schizophrenic in-patients and out-patients, when age and duration of illness were accounted for[]. Pine and Levinson[75] argued the relation of a patient to a mental hospital can be described as “patienthood” and claimed that those patients who become resident in a mental hospital voluntarily are like college students. Although being a patient in a mental hospital consists of punishment and stigma similar to being incarcerated in prison, the admission can also be seen as an opportunity for personal growth and social advancement like going away to university particularly when patients can adapt and adjust to their physical environment, staff and other admitted patients.

The theme of patient’s adaptive behaviour has been part of the literature throughout the whole period covered by this review. However, after the 1960s, only a small share of the identified papers covers this theme. The significant reduced emphasis on patient’s adaptive behaviour as a theme over time might have been introduced by the change in the mental health care model, from providing care in institutions in remote area to care in the community. Patients now are living and being cared for in new settings in the community.

Discussion

Four different meanings of how ‘institutionalization’ in psychiatry is conceptualized were identified from sixty-one papers across eleven different countries, i.e. bricks and mortar of care institutions, policy and legal frameworks regulating care, clinical responsibility and paternalism in clinician-patient relationships, and patients’ adaptive behavior to institutionalized care. These four identified connotations of how the term has been used in literature are conceptually distinct, but appear to overlap. Seventeen papers contained more than one of the four themes which may illustrate the complexity of the concept of institutionalization.

The conceptualization of institutionalization in psychiatry appears to have changed over time along with the changes in the provision of mental health care. Prior to the movement of deinstitutionalization, old-style mental hospitals functioned merely as a custodial care model and thus the perspective of bricks and mortar prevailed. The term ‘deinstitutionalization’ describes the process of downsizing and closing large hospitals accompanied by the establishment of alternative community-based mental health services[76,77]. As a result of the process of deinstitutionalization, many long-term hospitalized patients then were discharged into the community. It was found that the discharged patients experienced a higher quality of life compared to the hospitalized patients. Examples for such research are the studies of the Team for the Assessment of Psychiatric Services (TAPS) in North London[] and the Berlin De-Institutionalization study[79]. Discharged patients reported better satisfaction with their living conditions and had acquired friends and confidants. In addition, they gained domestic and community living skills, although no change was found in the patients’ clinical state or in their problems of social behavior. In modern psychiatry, however, the term ‘institutionalization’ goes beyond bricks and mortar as the functions of mental hospitals have changed. While in modern psychiatric hospitals less emphasis is put on institutionalizing patients with bricks and mortar, institutionalization is rather displayed in terms of policy and legal framework, in terms of clinical responsibility and paternalism or understood as patients’ response to institutional care. Although institutional organization and clinical responsibility aim to provide a structured and safe environment to facilitate the treatment process and to help monitor patients, they can also unintentionally institutionalize patients. Clinical paternalism can reinforce patients’ dependency on services, for instance, in the case of mandatory relationships between staff and patients where staff offer clinical paternalism- with the best intentions- to help patients manage their symptoms and life. Patients’ mental capacity to consent to treatment may also have to be considered in this context, but has so far received little attention in the literature on psychiatric institutionalization.

If paternalistic relationships between staff and patients reflect institutionalization, then institutionalization must not necessarily occur in a physical facility such as a mental hospital, but patients may also be subjected to being institutionalized in supported housing or supervised residential facilities with around the clock staffing as well as other alternative institutions in community settings (i.e. forensic hospitals). In addition, if institutionalization is conceptualized as patients’ response or adaptive behavior to services, then specialized community care such as assertive outreach could also be seen as a form of institutionalization due to the limited patient autonomy and their dependency on the intensive comprehensive care. Mental health patients residing in highly structured environments of community-based sheltered-care facilities can exhibit a distinct pattern of dependency[80]. Assertive Outreach (AO) has already been criticized for being paternalistic and coercive[]. Service users of AO teams live, work and socialize in the community as “free individuals” yet they remain subject to rules and restrictions as if contained in old fashioned asylums[]. Furthermore, patients who are legally mandated to receive treatment such as compulsory treatment in hospital or community might also be at risk of being institutionalized even though some argue involuntary psychiatric care helps to reduce symptoms, manage illness and re-establish a person’s ability to make autonomous decisions.

In conclusion, despite modern psychiatric services continuing to reflect the trend of deinstitutionalization with the closure of large mental hospitals, reduction of psychiatric hospital beds and the discharge of long-stay hospitalized patients into community, the findings of this review suggest that institutionalization can still manifest in alternative forms of community-based institutional settings. Therefore, there is a risk that mental health patients might also be subjected to new forms of institutionalization in community-based services, as conceptualized in the four identified themes. Although the establishment of community care aimed to promote patients’ autonomy and to provide care and treatment on a ‘partnership and consensual basis’ as much as possible, this review shows that institutionalization can still manifest in modern psychiatry similar to the old -style mental hospitals (asylums) beyond the traditional bricks and mortar hospital settings[,]. While patients may prefer community-based care to institutional ones, there is still a risk of subjecting mental health patients to institutionalization on psychiatric acute wards in general hospitals or new forms of residential facilities in community settings.

The results of this review can be related to critiques of Goffman’s notion of the mental institution[,] namely that the earlier conceptualizations of institutionalization are limiting and can no longer be applicable in today’s context. The traditional conceptualization of institutionalization reinforces mainly a restrictive understanding of institutionalization as taking place in institutions, where patients are only the sufferers of the treatment process and have limited autonomy and are completely isolated from the outside world. Townsend[] concluded in his review that studies from 1959 to 1975 support the idea that institutionalization involves patients accepting institutional life and developing a lack of desire to leave after a long stay in mental institutions. More recently, Quirk and his associates[,] found that ‘permeable institutions’ provide a better representation of the reality of everyday life in modern 'bricks and mortar' psychiatric institutions.

Strengths and limitations

One of the strengths of the review is that it considered literature from different disciplines and countries. Several main databases in the field were searched with broad search terms to avoid missing any major debates or discussions in the literature. In addition, the study team’s expertise in psychiatry, psychology and public health were utilized to identify patterns, combine related subject matters and minimize potential biases.

The review also has a number of limitations. Since the aim of this review is to search widely, relevant articles may have been missed but also literature that does not contain the search terms of this review explicitly. Also, conference presentations or grey literature were not included. The replicability of the review is limited given that establishing what information is relevant was based mainly on the individuals who are conducting the review. Finally, due to the focus of this review on the field of psychiatry, it has been beyond its scope to appraise how the term institutionalization is used in other disciplines. Consequently, a wide body of literature in the social sciences such as those examining the institutionalization of inmates, juvenile offenders or children in institutional care has been excluded.

Conclusions

The findings of the review emphasize that the term ‘institutionalization’ in modern psychiatry goes beyond definitions based on bricks and mortar, but rather includes ideas about staff’s responsibility, and policy and legal framework. Based on the traditional perspective of institutionalization, new services in the community can be seen as part of de-institutionalization. From the contemporary viewpoint however, one could argue that services such as supervised supported housing or assertive outreach may be a new form of institutional care since the movement of de-institutionalization.

The identified themes provide a preliminary framework for investigating and analyzing all care institutions in modern psychiatry, but do not constitute a coherent theoretical model of institutionalization. In this conceptual review, we neither started with an overarching theory nor developed one, but showed how institutionalization is understood in the field of psychiatry. This review highlights a number of fundamental elements to consider in further examination of the current and future development of institutional psychiatric care.

The findings have implications for further empirical research on (de)institutionalization. Tallying and analyzing the number of beds and places in mental health institutions facilitates health systems to examine and monitor their current state and future direction of mental health care institutions methodically. Moreover, provision of bed numbers in institutional settings can provide an indication of the trend of (de)institutionalization from a bricks and mortar perspective. Surprisingly, however, such data is difficult to obtain and clearer definitions and reliable sources are still required to investigate trends over time and even more so to compare internationally[,]. Thus more research is needed to fully understand the international development of mental health institutions. Yet, as this review showed, bed numbers in mental health institutions will not capture all of the different but interrelated aspects of psychiatric institutionalization. Therefore, quantitative research on trend(s) of (de)institutionalization should also include the development of other forms of psychiatric care, e.g. supervised supported housing, on the agenda. Also here, the availability of international data and identifying common definitions will be a major challenge. In spite of this, going beyond the bricks and mortar perspective in empirical research on (de)institutionalization will provide a valuable starting point for further quantitative and qualitative investigation of the underlying reasons for the changes in the provision of institutionalized mental health care.

To fully understand if and how alternative forms of psychiatric care can bring about a different form of institutionalization, it will be essential and worthwhile to adhere to the theme of patients’ adaptive behavior to care. This will shed light for a quantifiable approach to measure institutionalization in different contexts. Once more such research will lead to a thorough understanding of how patients respond or adapt to the different type of institutional psychiatric treatment, which will allow researchers to explore if a process of ‘psychiatric institutionalization’ is also apparent in other specialized modern forms of community mental health care model such as assertive outreach teams, early intervention teams and or crisis resolution terms.

From a public health perspective, institutionalization as policy and legal frameworks regulating care has been increasingly examined in the recent past as the rate of involuntary admission of people with mental illness has increased over the years[]. In taking a step forward, it will be fruitful to also include clinical paternalism and responsibility on the research agenda when looking at the effects of psychiatric institutionalization. For example, Sheehan and Burns’ findings[] indicated that high levels of perceived coercion are significantly associated with involuntary admission and a poor rating of therapeutic relationship. Voluntary hospitalization was seen as more coercive when patients rated their relationship with the admitting clinician negatively. The mental health field needs to assess the influence that paternalistic relationships and the unequal power relation between clinical staff and patient could have on the patient’s health condition and autonomy. More importantly, more empirical studies are needed to examine the benefits and harms of using informal coercion and practicing compulsory community psychiatric care.

In summary, the term ‘institutionalization’ is an evolving concept. Hence, further investigation of any of the four identified distinct but related themes will help develop a fuller understanding of (de)institutionalization and thus aid in clarifying the direction of mental health care in continuous discussions and future debates.

Competing interests

The authors declare that they have no conflicts of interest.

Authors’ contributions

WSC and SP were involved in the conception and design of the review. WSC conducted the literature search, interpreted data and drafted the manuscript. Both authors read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here:

Acknowledgements

We would like to thank Dr. Sara Dimic and Dr. Rose McCabe for being part of the study team and their guidance on refining the identified themes. This study was supported by a grant from East London NHS Foundation Trust.

References

  • Goffman E. Asylums; essays on the social situation of mental patients and other inmates. Garden City: Anchor Books; 1961. [Google Scholar]
  • Brown P. The mental patients’ rights movement and mental health institutional change. Int J Health Serv. 1981;11:523–540. doi: 10.2190/CU8G-D0RJ-YY54-UC3F. [PubMed] [CrossRef] [Google Scholar]
  • Leff J, Trieman N, Knapp M, Carrier J. Mental health. Beyond the asylum. Health Serv J. 1995;105:28–30. [PubMed] [Google Scholar]
  • de Girolamo G, Cozza M. The Italian Psychiatric Reform - a 20 years perspective. Int J Law Psychiatry. 2000;23:197–214. doi: 10.1016/S0160-2527(00)00030-3. [PubMed] [CrossRef] [Google Scholar]
  • Pedersen PB, Kolstad A. De-institutionalisation and trans-institutionalisation - changing trends of inpatient care in Norwegian mental health institutions 1950–2007. Int J Ment Health Syst. 2009;3:28. doi: 10.1186/1752-4458-3-28.[PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Bauer M, Kunze H, Von Cranach M, Fritze J, Becker T. Psychiatric reform in Germany. Psychiatric Reform in Europe. Acta Psychiatr Scand Suppl. 2001;410:27–34. [PubMed] [Google Scholar]
  • McCulloch A, Muijen M, Harper H. New developments in mental health policy in the United Kingdom. Int J Law Psychiatry. 2000;23:261–276. doi: 10.1016/S0160-2527(00)00038-8. [PubMed] [CrossRef] [Google Scholar]
  • Fakhoury W, Priebe S. The process of deinstitutionalization: an international overview. Curr Opin Psychiatr. 2002;15:187–192. doi: 10.1097/00001504-200203000-00011. [CrossRef] [Google Scholar]
  • Muijen M. Focus on mental health care reforms in Europe. Mental health services in Europe: an overview. Psychiatr Serv. 2008;59:479–482. doi: 10.1176/appi.ps.59.5.479. [PubMed] [CrossRef] [Google Scholar]
  • Turner T, Priebe S. Forget community care–reinstitutionalisation is here. Br J Psychiatry. 2002;181:253. doi: 10.1192/bjp.181.3.253. [PubMed] [CrossRef] [Google Scholar]
  • Priebe S, Badesconyi A, Fioritti A, Hansson L, Kilian R, Torres-Gonzales F, Turner T, Wiersma D. Reinstitutionalisation in mental health care: comparison of data on service provision from six European countries. BMJ. 2005;330:123–126. doi: 10.1136/bmj.38296.611215.AE.[PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Priebe S, Frottier P, Gaddini R, Kilian R, Lauber C, Martínez-Leal R, Munk-Jørgensen P, Walsh D, Wiersma D, Wright D. Mental health care institutions in nine European countries, 2002 to 2006. Psychiatr Serv. 2008;59:570–573. doi: 10.1176/appi.ps.59.5.570. [PubMed] [CrossRef] [Google Scholar]
  • Saxena S, Sharan P, Saraceno B. Budget and financing of mental health services: baseline information on 89 countries from WHO's project atlas. J Ment Health Policy Econ. 2003;6:135–143. [PubMed] [Google Scholar]
  • Lilford RJ, Richardson A, Stevens A, Fitzpatrick R, Edwards S, Rock F, Hutton JL. Issues in methodological research: perspectives from researchers and commissioners. Health Technol Assess. 2001;5:1–57. [PubMed] [Google Scholar]
  • Weinstein RM. Goffman's Asylums and the total institution model of mental hospitals. Psychiatry. 1994;57:348–367. [PubMed] [Google Scholar]
  • Saxena S, Thornicroft G, Knapp M, Whiteford H. Resources for mental health: scarcity, inequity, and inefficiency. Lancet. 2007;370:878–889. doi: 10.1016/S0140-6736(07)61239-2. [PubMed] [CrossRef] [Google Scholar]
  • Ritchie JA, Spencer L. In: The qualitative research companion. Huberman AM, Miles MB, editor. Thousand Oaks, California: Sage Publications; 2002. Data analysis for applied policy research; pp. 305–329. [Google Scholar]
  • Priebe S. Institutionalization revisited – with and without walls. Acta Psychiatr Scand. 2004;110:81–82. doi: 10.1111/j.1600-0047.2004.00386.x. [PubMed] [CrossRef] [Google Scholar]
  • Boardman A, Hodgson R. Community in-patient units and halfway hospitals. Adv Psychiatr Treat. 2000;6:120–127. doi: 10.1192/apt.6.2.120. [CrossRef] [Google Scholar]
  • Quirk A, Lelliott P, Seale C. The permeable institution: an ethnographic study of three acute psychiatric wards in London. Soc Sci Med. 2006;63:2105–2117. doi: 10.1016/j.socscimed.2006.05.021. [PubMed] [CrossRef] [Google Scholar]
  • Johnson SH, Gilburt B, Lloyd-Evans B, Osborn DP, Boardman J, Leese M, Shepherd G, Thornicroft G, Slade M. In-patient and residential alternatives to standard acute psychiatric wards in England. Br J Psychiatry. 2009;194:456–463. doi: 10.1192/bjp.bp.108.051698. [PubMed] [CrossRef] [Google Scholar]
  • Dvoski JA, Radomski S, Bennett C, Olin J, Hawkins R, Dotson L, Drewnicky I. Architectural design of a secure forensic state psychiatric hospital. Behav Sci. 2002;20:481–493. doi: 10.1002/bsl.506. [PubMed] [CrossRef] [Google Scholar]
  • Moos RH. Size, staffing, and psychiatric ward treatment environments. Arch Gen Psychiatry. 1972;26:414–418. doi: 10.1001/archpsyc.1972.01750230024005. [PubMed] [CrossRef] [Google Scholar]
  • Moos RH. Changing the social milieus of psychiatric treatment settings. J Appl Behav Sci. 1973;9:575–593. doi: 10.1177/002188637300900503. [CrossRef] [Google Scholar]
  • Taj R, Sheehan J. Architectural design and acute psychiatric care. Psychiatr Bull. 1994;18:279–281. doi: 10.1192/pb.18.5.279. [CrossRef] [Google Scholar]
  • Sine DM. The architecture of madness and the good of paternalism. Psychiatr Serv. 2008;59:1060–1062. doi: 10.1176/appi.ps.59.9.1060. [PubMed] [CrossRef] [Google Scholar]
  • Davis C, Glick ID, Rosow I. The architectural design of a psychotherapeutic milieu. Hosp Community Psychiatry. 1979;30:453–460. [PubMed] [Google Scholar]
  • Karlin BE, Zeiss RA. Best practices: environmental and therapeutic issues in psychiatric hospital design: toward best practices. Psychiatr Serv. 2006;57:1376–1378. doi: 10.1176/appi.ps.57.10.1376. [PubMed] [CrossRef] [Google Scholar]
  • Coldefy M, Curtis S. The geography of institutional psychiatric care in France 1800–2000: Historical analysis of the spatial diffusion of specialised facilities for institutional care of mental illness. Soc Sci Med. 2010;2010(71):2117–2129. [PubMed] [Google Scholar]
  • Gomia L, Walker B, Vogelpohl R, Eccard M, Lessing D, McCreery G, Paul M, Guist C. Twenty-four hours in a psychiatric hospital. A J of Nurs. 1970;70:1734–1736.[Google Scholar]
  • Rittmannsberger H, Sartorius N, Brad M, Burtea V, Capraru N, Cernak P, Dernovçek M, Dobrin I, Frater R, Hasto J, Hategan M, Haushofer M, Kafka J, Kasper S, Macrea R, Nabelek L, Nawka P, Novotny V, Platz T, Pojar A, Silberbauer C, Fekete S, Wancata J, Windhager E, Zapotoczky HG, Zöchling R. Changing aspects of psychiatric inpatient treatment. A census investigation in five European countries. Eur Psychiatry. 2004;19:483–488. doi: 10.1016/j.eurpsy.2004.05.001. [PubMed] [CrossRef] [Google Scholar]
  • van der Merwe M, Bowers L, Jones J, Simpson A, Haglund K. Locked doors in acute inpatient psychiatry: a literature review. J Psychiatr Ment Health Nurs. 2009;16:293–299. doi: 10.1111/j.1365-2850.2008.01378.x. [PubMed] [CrossRef] [Google Scholar]
  • Haglund K, van der Meiden E, von Knorring L, von Essen L. Psychiatric care behind locked doors. A study regarding the frequency of and the reasons for locked psychiatric wards in Sweden. J Psychiatr Ment Health Nurs. 2007;14:49–54. [PubMed] [Google Scholar]
  • Bowers L, Crowhurst N, Alexander J, Callaghan P, Eales S, Guy S, McCann E, Ryan C. Safety and security policies on psychiatric acute admission wards: results from a London-wide survey. J Psychiatr Ment Health Nurs. 2002;9:427–433. doi: 10.1046/j.1365-2850.2002.00492.x. [PubMed] [CrossRef] [Google Scholar]
  • Lang U. Do locked doors in psychiatric hospitals prevent patients from absconding? Eur J Psychiat. 2010;24:199–204.[Google Scholar]
  • Lewis DM. Responding to a violent incident: physical restraint or anger management as therapeutic interventions. J Psychiatr Ment Health Nurs. 2002;9:57–63. doi: 10.1046/j.1351-0126.2001.00440.x. [PubMed] [CrossRef] [Google Scholar]
  • Georgieva I, Mulder CL, Wierdsma A. Patients' preference and experiences of forced medication and seclusion. Psychiatr Q. 2012;83:1–13. doi: 10.1007/s11126-011-9178-y.[PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • McNown Johnson M, Rhodes R. Institutionalization: a theory of human behavior and the social environment. Adv Soc Work. 2007;8:219–236.[Google Scholar]
  • Zinkler M, Priebe S. Detention of the mentally ill in Europe–a review. Acta Psychiatr Scand. 2002;106:3–8. doi: 10.1034/j.1600-0447.2002.02268.x. [PubMed] [CrossRef] [Google Scholar]
  • Salize HJ, Dressingm H. Epidemiology of involuntary placement of mentally ill people across the European Union. Br J Psychiatry. 2004;2004(184):163–168. [PubMed] [Google Scholar]
  • Katsakou C, Priebe S. Outcomes of involuntary hospital admission–a review. Acta Psychiatr Scand. 2006;114:232–241. doi: 10.1111/j.1600-0447.2006.00823.x. [PubMed] [CrossRef] [Google Scholar]
  • Katsakou C, Bowers L, Amos T, Morriss R, Rose D, Wykes T, Priebe S. Coercion and treatment satisfaction among involuntary patients. Psychiatr Serv. 2010;61:286–292. doi: 10.1176/appi.ps.61.3.286. [PubMed] [CrossRef] [Google Scholar]
  • Priebe S, Katsakou C, Glöckner M, Dembinskas A, Fiorillo A, Karastergiou A, Kiejna A, Kjellin L, Nawka P, Onchev G, Raboch J, Schuetzwohl M, Solomon Z, Torres-González F, Wang D, Kallert T. Patients' views of involuntary hospital admission after 1 and 3 months: prospective study in 11 European countries. Br J Psychiatry. 2010;196:179–185. doi: 10.1192/bjp.bp.109.068916. [PubMed] [CrossRef] [Google Scholar]
  • Molodynki A, Rugkåsa J, Burns T. Coercion and compulsion in community mental health care. Br Med Bull. 2010;95:105–119. doi: 10.1093/bmb/ldq015. [PubMed] [CrossRef] [Google Scholar]
  • Reumschuessel-Wienert C, Crefeld W. Geschlossene psychiatrische Wohnheime [Closed Psychiatric Homes] Psychia Prax. 2012;39:4–6. doi: 10.1055/s-0031-1276995. [PubMed] [CrossRef] [Google Scholar]
  • Talbott JA, Glick ID. The inpatient care of the chronically mentally ill. Schizophr Bull. 1986;12:129–140. doi: 10.1093/schbul/12.1.129. [PubMed] [CrossRef] [Google Scholar]
  • Eklund M, Hansson L. Relationships between characteristics of the ward atmosphere and treatment outcome in a psychiatric day-care unit based on occupational therapy. Acta Psychiatr Scand. 1997;95:329–335. doi: 10.1111/j.1600-0447.1997.tb09640.x. [PubMed] [CrossRef] [Google Scholar]
  • Wasow M. The need for asylum for the chronically mentally ill. Schizophr Bull. 1986;12:162–167. doi: 10.1093/schbul/12.2.162. [PubMed] [CrossRef] [Google Scholar]
  • Wing JK. The functions of asylum. Br J Psychiatry. 1990;157:822–827. doi: 10.1192/bjp.157.6.822. [PubMed] [CrossRef] [Google Scholar]
  • O'Brien L, Cole R. Close-observation areas in acute psychiatric units: a literature review. Int J Ment Health Nurs. 2003;12:165–176. doi: 10.1046/j.1440-0979.2003.t01-1-00286.x. [PubMed] [CrossRef] [Google Scholar]
  • Prior P. Surviving psychiatric institutionalization: a case study. Social Health Ill. 1995;17:651–667. doi: 10.1111/1467-9566.ep10932141. [CrossRef] [Google Scholar]
  • Owen C, Tarantello C, Jones M, Tennant C. Violence and aggression in psychiatric units. Psychiatr Serv. 1998;49:1452–1457. [PubMed] [Google Scholar]
  • Nijman HL, aCampo JM, Ravelli DP, Merckelbach HL. A tentative model of aggression on inpatient psychiatric wards. Psychiatr Serv. 1999;50:832–834. [PubMed] [Google Scholar]
  • Killaspy H. From the asylum to community care: learning from experience. Br Med Bull. 2006;79–80:245–258. [PubMed] [Google Scholar]
  • Canvin K, Bartleet A, Pinfold V. Acceptability of compulsory powers in the community: the ethical considerations of mental health service users on supervised discharge and guardianship. J Med Ethics. 2005;31:457–462. doi: 10.1136/jme.2003.004861.[PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Quirk A, Lelliott P. What do we know about life on acute psychiatric wards in the UK? A review of the research evidence. Soc Sci Med. 2001;53:1565–1574. doi: 10.1016/S0277-9536(00)00457-3. [PubMed] [CrossRef] [Google Scholar]
  • Sheehan KA, Burns T. Perceived coercion and the therapeutic relationship: a neglected association? Psychiatr Serv. 2011;62:471–476. doi: 10.1176/appi.ps.62.5.471. [PubMed] [CrossRef] [Google Scholar]
  • Priebe S, Katsakou C, Amos T, Leese M, Morriss R, Rose D, Wykes T, Yeeles K. Patients' views and readmissions 1 year after involuntary hospitalisation. Br J Psychiatry. 2009;194:49–54. doi: 10.1192/bjp.bp.108.052266. [PubMed] [CrossRef] [Google Scholar]
  • McCubbin M, Cohen D. A systemic and value-based approach to strategic reform of the mental health system. Health Care Anal. 1999;7:57–77. doi: 10.1023/A:1009443902415. [PubMed] [CrossRef] [Google Scholar]
  • Lay B, Nordt C, Rössler W. Variation in use of coercive measures in psychiatric hospitals. Eur Psychiatry. 2011;26:244–251. [PubMed] [Google Scholar]
  • Lützén K. Subtle coercion in psychiatric practice. J Psychiatr Ment Health Nurs. 1998;5:101–107. doi: 10.1046/j.1365-2850.1998.00104.x. [PubMed] [CrossRef] [Google Scholar]
  • Jarrett M, Bowers L, Simpson A. Coerced medication in psychiatric inpatient care: literature review. J Adv Nurs. 2008;64:538–548. doi: 10.1111/j.1365-2648.2008.04832.x. [PubMed] [CrossRef] [Google Scholar]
  • Wing JK. Institutionalism and institutionalization. J Forensic Psychiatr. 1962;11:7–10.[Google Scholar]
  • Wing JK, Brown GW. Institutionalism and schizophrenia: a comparative study of three mental hospitals, 1960–1968. London: Cambridge University Press; 1970. [Google Scholar]
  • Karmel M. Total institution and self-mortification. J Health Soc Behav. 1969;10:134–141. doi: 10.2307/2948361. [PubMed] [CrossRef] [Google Scholar]
  • Curson DA, Pantelis C, Ward J, Barnes TR. Institutionalism and schizophrenia 30 years on. Clinical poverty and the social environment in three British mental hospitals in 1960 compared with a fourth in 1990. Br J Psychiatry. 1992;160:230–241. doi: 10.1192/bjp.160.2.230. [PubMed] [CrossRef] [Google Scholar]
  • Wing JK, Brown GW. Social treatment of chronic schizophrenia: a comparative survey of three hospitals. J Ment Sci. 1961;107:847.[Google Scholar]
  • Ochberg FM, Zarcone V, Hamburg DA. Symposium on institutionalism. Compr Psychiatry. 1972;13:91–104. doi: 10.1016/0010-440X(72)90014-4. [PubMed] [CrossRef] [Google Scholar]
  • Barton R. The patient's personal territory. Hosp Community Psychiatry. 1966;17:336. [PubMed] [Google Scholar]
  • Liberakis EA. Factors predisposing to institutionalism. Acta Psychiatr Scand. 1981;63:357–366. [PubMed] [Google Scholar]
  • Rosenhan DL. On being sane in insane places. Science. 1973;179:250–258. doi: 10.1126/science.179.4070.250. [PubMed] [CrossRef] [Google Scholar]
  • Ford R, Durcan G, Warner L, Hardy P, Muijen M. One day survey by the Mental Health Act Commission of acute adult psychiatric inpatient wards in England and Wales. BMJ. 1998;317:1279–1283. doi: 10.1136/bmj.317.7168.1279.[PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Gruenberg EM. The social breakdown syndrome–some origins. Am J Psychiatry. 1967;123:1481–1489. [PubMed] [Google Scholar]
  • Johnstone EC, Owens DG, Gold A, Crow TJ, MacMillan JF. Institutionalization and the defects of schizophrenia. Br J Psychiatry. 1981;139:195–203. doi: 10.1192/bjp.139.3.195. [PubMed] [CrossRef] [Google Scholar]
  • Pine F, Levinson DJ. A sociopsychological conception of patienthood. Int. J. of Soc. 1961;7:106–123.[Google Scholar]
  • Szmukler GF, Holloway F. In: Textbook of community psychiatry. Thornicroft G, Szmukler G, editor. Oxford: Oxford University Press; 2001. In-patient treatment; pp. 321–338. [Google Scholar]
  • Leff J, Trieman N, Knapp M. The TAPS Project: a report on 13 years of research, 1985–1998. Psychiatr Bull. 2000;24:165–168. doi: 10.1192/pb.24.5.165. [CrossRef] [Google Scholar]
  • Priebe S, Hoffmann K, Iserman M, Kaiser W. Do long-term hospitalised patients benefit from discharge into the community? Soc Psychiatry Psychiatr Epidemiol. 2002;37:387–392. doi: 10.1007/s00127-002-0568-1. [PubMed] [CrossRef] [Google Scholar]
  • Segal C, Moyles E. Management and Institutional dependency in sheltered care. Soc Psychiatr. 1979;14:159–165. doi: 10.1007/BF00577866. [CrossRef] [Google Scholar]
  • Halpern A, Szmukler G. Psychiatric advance directives: reconciling autonomy and non-consensual treatment. Psychiatr Bull. 1997;21:323–327. doi: 10.1192/pb.21.6.323. [CrossRef] [Google Scholar]
  • Crawford MJ, Rutter D, Manley C, Weaver T, Bhui K, Fulop N, Tyrer P. Systematic review of involving patients in the planning and development of health care. BMJ. 2002;325:1263. doi: 10.1136/bmj.325.7375.1263.[PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Townsend JM. Self-concept and the institutionalization of mental patients: an overview and critique. J Health Soc Behav. 1976;17:263–271. doi: 10.2307/2136547. [PubMed] [CrossRef] [Google Scholar]
  • Weinstein RM. Patient attitudes toward mental hospitalization: a review of quantitative research. J Health Soc Behav. 1979;20:237–258. doi: 10.2307/2136449. [PubMed] [CrossRef] [Google Scholar]
  • Mundt AP, Frančišković T, Gurovich I, Heinz A, Ignatyev Y, Ismayilov F, Kalapos MP, Krasnov V, Mihai A, Mir J, Padruchny D, Potočan M, Raboch J, Taube M, Welbel M, Priebe S. Changes in the provision of institutionalized mental health care in post-communist countries. PLoS One. 2012;7:e38490. doi: 10.1371/journal.pone.0038490.[PMC free article] [PubMed] [CrossRef] [Google Scholar]
  • Mir J, Priebe S, Mundt AP. People with mental disorders in East and West Germany: Indicators of institutionalized care since reunification. Nervenarzt. 2012. pp. 1–7. [PubMed] [CrossRef]
Articles from BMC Psychiatry are provided here courtesy of BioMed Central
« Previous: Epilogue: A TANGLED MULTILAYERED WEB
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Aboitiz F (2012) Gestures, vocalizations, and memory in language origins. Front Evol Neurosci 4:2.

Ache BW, Young JM (2005) Olfaction: Diverse species, conserved principles. Neuron 48: 417–430.

Adams DL, Horton JC (2003) Capricious expression of cortical columns in the primate brain. Nat Neurosci 6:113–114.

Adams EDM, Goss GG, Leys SP, Launikonis BS (2010) Freshwater sponges have functional, sealing epithelia with high transepithelial resistance and negative transepithelial potential. PLoS ONE 5:e15040.

Adoutte A, Balavoine G, Lartillot N, Lespinet O, Prud’homme B, de Rosa R (2000) The new animal phylogeny: Reliability and implications. Proc Natl Acad Sci USA 97:4453–4456.

Aiello LC, Wheeler P (1995) The expensive tissue hypothesis: The brain and the digestive system in human and primate evolution. Curr Anthropol 36:199–221.

Airey DC, Castillo-Juarez H, Casella G, Pollak EJ, DeVoogd TJ (2000) Variation in the volume of zebra finch song control nuclei is heritable: Developmental and evolutionary implications. Proc Biol Sci 267:2099–2104.

Aksay E, Baker R, Seung HS, Tank DW (2000) Anatomy and discharge properties of premotor neurons in the goldfish medulla that have eye-position signals during fixations. J Neurophysiol 84:1035–1049.

Aksay E, Gamkrelidze G, Seung HS, Baker R, Tank DW (2001) In vivo intracellular recording and perturbation of persistent activity in a neural integrator. Nat Neurosci 4:184–193.

Aksay E, Baker R, Seung HS, Tank DW (2003) Correlated discharge among cell pairs within the oculomotor horizontal velocity-to-position integrator. J Neurosci 23:10852–10858.

Alberch P (1989) The logic of monsters: Evidence for internal constraint in development and evolution. Geobios Mem Spec 12:21–57.

Albus K, Beckmann R (1980) Second and third visual areas of the cat: Interindividual variability in retinotopic arrangement and cortical location. J Physiol 299:247–276.

Amrein I, Dechmann DKN, Winter Y, Lipp H-P (2007) Absent or low rate of adult neurogenesis in the hippocampus of bats (Chiroptera). PLoS ONE 2:e455.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Anderson JT, Smith LM (2000) Invertebrate response to moist-soil management of playa wetlands. Ecol Appl 10:550–558.

Anderson ML (2010) Neural reuse: A fundamental organizational principle of the brain. Behav Brain Sci 33:245–266.

Anderson PA, Olavarria J, Van Sluyters RC (1988) The overall pattern of ocular dominance bands in cat visual cortex. J Neurosci 8:2183–2200.

Anderson PAV, Greenberg RM (2001) Phylogeny of ion channels: Clues to structure and function. Comp Biochem Physiol B Biochem Mol Biol 129:17–28. Available at http://www.journals.elsevier.com/comparative-biochemistry-and-physiology-part-b-biochemistry-and-molecular-biology/.

Andres KH, von Düring M, Iggo A, Proske U (1991) The anatomy and fine structure of the echidna Tachyglossus aculeatus snout with respect to its different trigeminal sensory receptors including the electroreceptors. Anat Embryol (Berl) 184:371–393.

Ansari D (2008) Effects of development and enculturation on number representation in the brain. Nat Rev Neurosci 9:278–291.

Ansari D, Garcia N, Lucas E, Hamon K, Dhital B (2005) Neural correlates of symbolic number processing in children and adults. Neuroreport 16:1769–1773.

Arabidopsis Interactome Mapping Consortium (2011) Evidence for network evolution in an Arabidopsis interactome map. Science 333:601–607.

Arcese P, Sogge MK, Marr AB, Patten MA (2002) Song sparrow (Melospiza melodia). Birds North Am 704:1–40.

Arendt D, Nübler-Jung K (1997) Dorsal or ventral: Similarities in fate maps and gastrulation patterns in annelids, arthropods and chordates. Mech Dev 61:7–21.

Arendt D, Denes AS, Jékely G, Tessmar-Raible K (2008) The evolution of nervous system centralization. Philos Trans R Soc Lond B Biol Sci 363:1523–1528.

Argollo de Menezes M, Moukarzel C, Penna TJP (2000) First-order transition in small world networks. Europhys Lett 50:574–579.

Aristotle, Waterfield R, Bostock D (2008) Physics (Oxford Univ Press, Oxford), p 301.

Arnegard ME, Zwickl DJ, Lu Y, Zakon HH (2010) Old gene duplication facilitates origin and diversification of an innovative communication system—twice. Proc Natl Acad Sci USA 107:22172–22177.

Arshavsky Y, Deliagina TG, Orlovsky GN, Panchin YuV, Pavlova GA, Popova LB (1986) Control of locomotion in marine mollusc Clione limacina. VI. Activity of isolated neurons of pedal ganglia. Exp Brain Res 63:106–112.

Arshavsky YI, Deliagina TG, Orlovsky GN, Panchin YV, Popova LB (1992) Interneurones mediating the escape reaction of the marine mollusc Clione limacina. J Exp Biol 164:307–314.

Arzi A, Sobel N (2011) Olfactory perception as a compass for olfactory neural maps. Trends Cogn Sci 15:537–545.

Ashwell KWS, Hardman CD, Paxinos G (2006) Cyto- and chemoarchitecture of the sensory trigeminal nuclei of the echidna, platypus and rat. J Chem Neuroanat 31:81–107.

Atema J (1996) Eddy chemotaxis and odor landscapes: Exploration of nature with animal sensors. Biol Bull 191:129–138.

Attwell D, Laughlin SB (2001) An energy budget for signaling in the grey matter of the brain. J Cereb Blood Flow Metab 21:1133–1145.

Audesirk G (1978) Central neuronal control of cilia in Tritonia diamedia. Nature 272:541–543.

Audesirk G, McCaman RE, Willows AOD (1979) The role of serotonin in the control of pedal ciliary activity by identified neurons in Tritonia diomedia. Comp Biochem Physiol 62C:87–91.

Auerbach AA, Bennett MVL (1969) A rectifying electrotonic synapse in the central nervous system of a vertebrate. J Gen Physiol 53:211–237.

Averof M, Patel NH (1997) Crustacean appendage evolution associated with changes in Hox gene expression. Nature 388:682–686.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Avise, JC, Ayala FJ, eds (2007) In the Light of Evolution Volume I: Adaptation and Complex Design (National Academies Press, Washington, DC).

Avise JC, Ayala FJ, eds (2009) In the Light of Evolution. Volume III: Two Centuries of Darwin (National Academies Press, Washington, DC).

Avise JC, Ayala FJ, eds (2010) In the Light of Evolution. Volume IV: The Human Condition (National Academies Press, Washington, DC).

Avise JC, Hubbell SP, Ayala FJ, eds (2008) In the Light of Evolution. Volume II: Biodiversity and Extinction (National Academies Press, Washington, DC).

Ayala FJ (1986) On the virtues and pitfalls of the molecular evolutionary clock. J Hered 77:226–235.

Ayala FJ (1997) Vagaries of the molecular clock. Proc Natl Acad Sci USA 94:7776–7783.

Azevedo FAC, Carvalho LR, Grinberg LT, Farfel JM, Ferretti RE, Leite RE, Jacob Filho W, Lent R, Herculano-Houzel S (2009) Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain. J Comp Neurol 513:532–541.

Azzopardi P, Cowey A (1993) Preferential representation of the fovea in the primary visual cortex. Nature 361:719–721.

Baek M (2011) Development of leg motor neurons in Drosophila melanogaster. PhD dissertation (Columbia University, New York).

Baldwin CY, Clark KB (2000) Design Rules: The Power of Modularity (MIT Press, Cambridge, MA), Vol 1.

Baldwin MKL, Kaskan PM, Zhang B, Chino YM, Kaas JH (2012) Cortical and subcortical connections of V1 and V2 in early postnatal macaque monkeys. J Comp Neurol 520:544–569.

Balsters JH, Cussans E, Diedrichsen J, Phillips KA, Preuss TM, Rilling JK, Ramnani N (2010) Evolution of the cerebellar cortex: The selective expansion of prefrontal-projecting cerebellar lobules. Neuroimage 49:2045–2052.

Barabási A-L, Oltvai ZN (2004) Network biology: Understanding the cell’s functional organization. Nat Rev Genet 5:101–113.

Barbas H (1988) Anatomic organization of basoventral and mediodorsal visual recipient prefrontal regions in the rhesus monkey. J Comp Neurol 276:313–342.

Barbas H, Mesulam MM (1985) Cortical afferent input to the principalis region of the rhesus monkey. Neuroscience 15:619–637.

Barbas H, Pandya DN (1989) Architecture and intrinsic connections of the prefrontal cortex in the rhesus monkey. J Comp Neurol 286:353–375.

Bargmann CI (1998) Neurobiology of the Caenorhabditis elegans genome. Science 282: 2028–2033.

Bargmann CI (2006) Comparative chemosensation from receptors to ecology. Nature 444: 295–301.

Barone P, Dehay C, Berland M, Kennedy H (1996) Role of directed growth and target selection in the formation of cortical pathways: Prenatal development of the projection of area V2 to area V4 in the monkey. J Comp Neurol 374:1–20.

Barraclough NE, Xiao D, Baker CI, Oram MW, Perrett DI (2005) Integration of visual and auditory information by superior temporal sulcus neurons responsive to the sight of actions. J Cogn Neurosci 17:377–391.

Barres BA (2008) The mystery and magic of glia: A perspective on their roles in health and disease. Neuron 60:430–440.

Barrett HC, Kurzban R (2006) Modularity in cognition: Framing the debate. Psychol Rev 113:628–647.

Barske J, Schlinger BA, Wikelski M, Fusani L (2011) Female choice for male motor skills. Proc R Soc B 278:3523–3528.

Bass AH, Baker R (1990) Sexual dimorphisms in the vocal control system of a teleost fish: Morphology of physiologically identified neurons. J Neurobiol 21:1155–1168.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Bass AH, Baker R (1991) Evolution of homologous vocal control traits. Brain Behav Evol 38:240–254.

Bass AH, Baker R (1997) Phenotypic specification of hindbrain rhombomeres and the origins of rhythmic circuits in vertebrates. Brain Behav Evol 50(Suppl 1):3–16.

Bass AH, Chagnaud BP (2012) Shared evolutionary and developmental origins for neural basis of vocal-acoustic and pectoral-gestural signaling. Proc Natl Acad Sci USA 109(Suppl 1):10677-10684.

Bass AH, Ladich F (2008) Vocal-acoustic communication: From neurons to behavior. In Fish Bioacoustics, eds Webb JF, Fay RR, Popper AN (Springer, Berlin), pp 253–278.

Bass AH, McKibben JR (2003) Neural mechanisms and behaviors for acoustic communication in teleost fish. Prog Neurobiol 69:1–26.

Bass AH, Remage-Healey L (2008) Central pattern generators for social vocalization: Androgen-dependent neurophysiological mechanisms. Horm Behav 53:659–672.

Bass AH, Zakon HH (2005) Sonic and electric fish: At the crossroads of neuroethology and behavioral neuroendocrinology. Horm Behav 48:360–372.

Bass AH, Marchaterre MA, Baker R (1994) Vocal-acoustic pathways in a teleost fish. J Neurosci 14:4025–039.

Bass AH, Gilland EH, Baker R (2008) Evolutionary origins for social vocalization in a vertebrate hindbrain-spinal compartment. Science 321:417–421.

Bassett DS, Meyer-Lindenberg A, Achard S, Duke T, Bullmore E (2006) Adaptive reconfiguration of fractal small-world human brain functional networks. Proc Natl Acad Sci USA 103:19518–19523.

Beauchamp MS, Nath AR, Pasalar S (2010) fMRI-guided transcranial magnetic stimulation reveals that the superior temporal sulcus is a cortical locus of the McGurk effect. J Neurosci 30:2414–2417.

Beaulieu C, Colonnier M (1985) A laminar analysis of the number of round-asymmetrical and flat-symmetrical synapses on spines, dendritic trunks, and cell bodies in area 17 of the cat. J Comp Neurol 231:180–189.

Bebbington A, Hughes GM (1973) Locomotion in Aplysia (Gastropoda, Opisthobranchia). J Molluscan Stud 40:399–405.

Behrens DW (2005) Nudibranch Behavior (New World, Jacksonville, FL).

Bello BC, Hirth F, Gould AP (2003) A pulse of the Drosophila Hox protein Abdominal-A schedules the end of neural proliferation via neuroblast apoptosis. Neuron 37:209–219.

Belton E, Salmond CH, Watkins KE, Vargha-Khadem F, Gadian DG (2003) Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia. Hum Brain Mapp 18:194–200.

Bendesky A, Bargmann CI (2011) Genetic contributions to behavioural diversity at the gene-environment interface. Nat Rev Genet 12:809–820.

Bengtson S, Budd G (2004) Comment on “Small bilaterian fossils from 40 to 55 million years before the Cambrian.” Science 306:1291a.

Bengtson S, Zhao Y (1992) Predatorial borings in late Precambrian mineralized exoskeletons. Science 257:367–369.

Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate—a practical and powerful approach to multiple testing. J Roy Stat Soc B Met 57:289–300.

Bennett MVL (1971) Electric organs. In Fish Physiology, eds Hoar WS, Randall DJ (Academic, New York), Vol V, pp 347–491.

Benton MJ, Donoghue PCJ, Asher RJ (2009) Calibrating and constraining molecular clocks. In The Timetree of Life, eds Hedges SB, Kumar S (Oxford University Press, London), pp 35–86.

Bentourkia M, Bol A, Ivanoiu A, Labar D, Sibomana M, Coppens A, Michel C, Cosnard G, De Volder AG (2000) Comparison of regional cerebral blood flow and glucose metabolism in the normal brain: Effect of aging. J Neurol Sci 181:19–28.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Beran MJ, Beran MM (2004) Chimpanzees remember the results of one-by-one addition of food items to sets over extended time periods. Psychol Sci 15:94–99.

Berg J, Lässig M, Wagner A (2004) Structure and evolution of protein interaction networks: A statistical model for link dynamics and gene duplications. BMC Evol Biol 4:51.

Bertelson P, Aschersleben G (2003) Temporal ventriloquism: Crossmodal interaction on the time dimension. 1. Evidence from auditory-visual temporal order judgment. IntJ Psychophysiol 50:147–155.

Beshel J, Kopell N, Kay LM (2007) Olfactory bulb gamma oscillations are enhanced with task demands. J Neurosci 27:8358–8365.

Bharati IS, Goodson JL (2006) Fos responses of dopamine neurons to sociosexual stimuli in male zebra finches. Neuroscience 143:661–670.

Birkeland C (1974) Interactions between a sea pen and seven of its predators. Ecol Monogr 44:211–232.

Birket-Smith SJR (1981) A reconstruction of the pre-Cambrian Spriggina. Zool Jahrb Abt Anat 105:237–258.

Bishop KM, Rubenstein JL, O’Leary DD (2002) Distinct actions of Emx1, Emx2, and Pax6 in regulating the specification of areas in the developing neocortex. J Neurosci 22: 7627–7638.

Block BA, Finnerty JR, Stewart AF, Kidd J (1993) Evolution of endothermy in fish: Mapping physiological traits on a molecular phylogeny. Science 260:210–214.

Blondel VD, Guillaume J-L, Lambiotte R, Lefebvre E (2008) Fast unfolding of communities in large networks. J Stat Mech 10:P10008.

Bohnen NI, Minoshima S, Giordani B, Frey KA, Kuhl DE (1999) Motor correlates of occipital glucose hypometabolism in Parkinson’s disease without dementia. Neurology 52:541–546.

Boiko T, Van Wart A, Caldwell JH, Levinson SR, Trimmer JS, Matthews G (2003) Functional specialization of the axon initial segment by isoform-specific sodium channel targeting. J Neurosci 23:2306–2313.

Boire D, Baron G (1994) Allometric comparison of brain and main brain subdivisions in birds. J Hirnforsch 35:49–66.

Boles LC, Lohmann KJ (2003) True navigation and magnetic maps in spiny lobsters. Nature 421:60–63.

Bonhoeffer T, Grinvald A (1991) Iso-orientation domains in cat visual cortex are arranged in pinwheel-like patterns. Nature 353:429–431.

Bonkowsky JLJ, Chien C-BC (2005) Molecular cloning and developmental expression of foxP2 in zebrafish. Dev Dyn 234:740–746.

Bonn C, Cantlon JF (2012) The origins and structure of quantitative concepts. Cognitive Neuropsychology, in press.

Bonner JT (2006) Why Size Matters: From Bacteria to Blue Whales (Princeton Univ Press, Princeton, NJ).

Bopp D, Burri M, Baumgartner S, Frigerio G, Noll M (1986) Conservation of a large protein domain in the segmentation gene paired and in functionally related genes of Drosophila. Cell 47:1033–1040.

Boroditsky L (2000) Metaphoric structuring: Understanding time through spatial metaphors. Cognition 75:1–28.

Bortoff GA, Strick PL (1993) Corticospinal terminations in two New-World primates: Further evidence that corticomotoneuronal connections provide part of the neural substrate for manual dexterity. J Neurosci 13:5105–5118.

Bossing T, Udolph G, Doe CQ, Technau GM (1996) The embryonic central nervous system lineages of Drosophila melanogaster. I. Neuroblast lineages derived from the ventral half of the neuroectoderm. Dev Biol 179:41–64.

Bostwick KS, Elias DO, Mason A, Montealegre-Z F (2010) Resonating feathers produce courtship song. Proc R Soc B 277:835–841.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Bottjer DJ, Clapham ME (2006) Evolutionary paleoecology of the Ediacaran benthic marine animals. In Neoproterozoic Geobiology and Paleobiology, eds Xiao S, Kaufman AJ (Springer, Berlin), pp 91–114.

Bouchet P, Rocroi J-P, eds (2005) Classification and nomenclator of gastropod families. Malacologia 47:1–368.

Bouvier MM, Mytilineou C (1995) Basic fibroblast growth factor increases division and delays differentiation of dopamine precursors in vitro. J Neurosci 15:7141–7149.

Boyan GS, Ball EE (1993) The grasshopper, Drosophila and neuronal homology (advantages of the insect nervous system for the neuroscientist). Prog Neurobiol 41:657–682.

Bradbury J, Vehrencamp S (2011) Principles of Animal Communication (Sinauer, Sunderland, MA).

Brannon EM, Terrace HS (1998) Ordering of the numerosities 1 to 9 by monkeys. Science 282:746–749.

Brannon EM, Lutz D, Cordes S (2006) The development of area discrimination and its implications for number representation in infancy. Dev Sci 9:F59–F64.

Brantley RK, Bass AH (1994) Alternative male spawning tactics and acoustic signals in the plainfin midshipman fish, Porichthys notatus (Teleostei, Batrachoididae). Ethology 96:213–232.

Brawand D, Soumillon M, Necsulea A, Julien P, Csárdi G, Harrigan P, Weier M, Liechti A, Aximu-Petri A, Kircher M, Albert FW, Zeller U, Khaitovich P, Grützner F, Bergmann S, Nielsen R, Pääbo S, Kaessmann H (2011) The evolution of gene expression levels in mammalian organs. Nature 478:343–348.

Brigandt I (2002) Homology and the origin of correspondence. Biol Philos 17:389–407.

Briggs DEG, Erwin DH, Collier FJ (1994) The Fossils of the Burgess Shale (Smithsonian Institution Press, Washington, DC).

Britten RJ (2002) Divergence between samples of chimpanzee and human DNA sequences is 5%, counting indels. Proc Natl Acad Sci USA 99:13633–13635.

Brodmann K (1909) Vergleichende Lokalisationslehre der Grosshirnrhinde (Barth, Leipzig).

Bromham L, Rambaut A, Fortey R, Cooper A, Penny D (1998) Testing the Cambrian explosion hypothesis by using a molecular dating technique. Proc Natl Acad Sci USA 95:12386–12389.

Bronchti G, Heil P, Sadka R, Hess A, Scheich H, Wollberg Z (2002) Auditory activation of “visual” cortical areas in the blind mole rat (Spalax ehrenbergi). Eur J Neurosci 16: 311–329.

Bruce AW, Donaldson IJ, Wood IC, Yerbury SA, Sadowski MI, Chapman M, Göttgens B, Buckley NJ (2004) Genome-wide analysis of repressor element 1 silencing transcription factor/neuron-restrictive silencing factor (REST/NRSF) target genes. Proc Natl Acad Sci USA 101:10458–10463.

Bruce CJ, Goldberg ME (1985) Primate frontal eye fields. I. Single neurons discharging before saccades. J Neurophysiol 53:603–635.

Brusca RC, Brusca GJ (2003) Invertebrates (Sinauer, Sunderland, MA), 2nd Ed, pp 479–482.

Buckner RL, Raichle ME, Petersen SE (1995) Dissociation of human prefrontal cortical areas across different speech production tasks and gender groups. J Neurophysiol 74: 2163–2173.

Budd GE, Telford MJ (2009) The origin and evolution of arthropods. Nature 457:812–817.

Bugden S, Ansari D (2011) Individual differences in children’s mathematical competence are related to the intentional but not automatic processing of Arabic numerals. Cognition 118:32–44.

Bukach CM, Gauthier I, Tarr MJ (2006) Beyond faces and modularity: The power of an expertise framework. Trends Cogn Sci 10:159–166.

Bull R, Scerif G (2001) Executive functioning as a predictor of children’s mathematics ability: Inhibition, switching, and working memory. Dev Neuropsychol 19:273–293.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Buller D (2005) Adapting Minds: Evolutionary Psychology and the Persistent Quest for Human Nature (MIT Press, Cambridge, MA).

Bullier J, Schall JD, Morel A (1996) Functional streams in occipito-frontal connections in the monkey. Behav Brain Res 76:89–97.

Bullock TH, Horridge GA (1965) Structure and Function in the Nervous Systems of Invertebrates (Freeman, San Francisco), Vols I and II.

Buonomano DV, Merzenich MM (1998) Cortical plasticity: From synapses to maps. Annu Rev Neurosci 21:149–186.

Bush EC, Allman JM (2003) The scaling of white matter to gray matter in cerebellum and neocortex. Brain Behav Evol 61:1–5.

Buss LW, Seilacher A (1994) The phylum Vendobionta: A sister group of the Eumetazoa? Paleobiology 20:1–4.

Bustamante CD, Fledel-Alon A, Williamson S, Nielsen R, Hubisz MT, Glanowski S, Tanenbaum DM, White TJ, Sninsky JJ, Hernandez RD, Civello D, Adams MD, Cargill M, Clark AG (2005) Natural selection on protein-coding genes in the human genome. Nature 437:1153–1157.

Butler AB (1994) The evolution of the dorsal thalamus of jawed vertebrates, including mammals: Cladistic analysis and a new hypothesis. Brain Res Brain Res Rev 19:29–65.

Buxhoeveden DP, Casanova MF (2002) The minicolumn hypothesis in neuroscience. Brain 125:935–951.

Buxhoeveden DP, Switala AE, Litaker M, Roy E, Casanova MF (2001) Lateralization of minicolumns in human planum temporale is absent in nonhuman primate cortex. Brain Behav Evol 57:349–358.

Byrne RW (1995) The Thinking Ape: Evolutionary Origins of Intelligence (Oxford Univ Press, Oxford).

Cáceres M, Lachuer J, Zapala MA, Redmond JC, Kudo L, Geschwind DH, Lockhart DJ, Preuss TM, Barlow C (2003) Elevated gene expression levels distinguish human from non-human primate brains. Proc Natl Acad Sci USA 100:13030–13035.

Cáceres M, Suwyn C, Maddox M, Thomas JW, Preuss TM (2007) Increased cortical expression of two synaptogenic thrombospondins in human brain evolution. Cereb Cortex 17:2312–2321.

Cai X (2008) Unicellular Ca2+ signaling “toolkit” at the origin of metazoa. Mol Biol Evol 25:1357–1361.

Calford MB, Graydon ML, Huerta MF, Kaas JH, Pettigrew JD (1985) A variant of the mammalian somatotopic map in a bat. Nature 313:477–479.

Call J, Tomasello M (2008) Does the chimpanzee have a theory of mind 30 years later. Trends Cogn Sci 12:187–192.

Calvert GA, Hansen PC, Iversen SD, Brammer MJ (2001) Detection of audio-visual integration sites in humans by application of electrophysiological criteria to the BOLD effect. Neuroimage 14:427–438.

Cambronero F, Puelles L (2000) Rostrocaudal nuclear relationships in the avian medulla oblongata: A fate map with quail chick chimeras. J Comp Neurol 427:522–545.

Campanella S, Belin P (2007) Integrating face and voice in person perception. Trends Cogn Sci 11:535–543.

Campbell JID (2005) Handbook of Mathematical Cognition (Psychology Press, New York).

Campi KL, Krubitzer L (2010) Comparative studies of diurnal and nocturnal rodents: Differences in lifestyle result in alterations in cortical field size and number. J Comp Neurol 518:4491–4512.

Campi KL, Collins CE, Todd WD, Kaas J, Krubitzer L (2011) Comparison of area 17 cellular composition in laboratory and wild-caught rats including diurnal and nocturnal species. Brain Behav Evol 77:116–130.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Campos-Ortega JA (1995) Genetic mechanisms of early neurogenesis in Drosophila melanogaster. Mol Neurobiol 10:75–89.

Cantlon JF, Brannon EM (2005) Semantic congruity affects numerical judgments similarly in monkeys and humans. Proc Natl Acad Sci USA 102:16507–16511.

Cantlon JF, Brannon EM (2006) Shared system for ordering small and large numbers in monkeys and humans. Psychol Sci 17:401–406.

Cantlon JF, Brannon EM (2007a) Basic math in monkeys and college students. PLoS Biol 5:e328.

Cantlon JF, Brannon EM (2007b) How much does number matter to a monkey (Macaca mulatta)? J Exp Psychol Anim Behav Process 33:32–41.

Cantlon JF, Brannon EM, Carter EJ, Pelphrey KA (2006) Functional imaging of numerical processing in adults and 4-y-old children. PLoS Biol 4:e125.

Cantlon JF, Cordes S, Libertus ME, Brannon EM (2009a) Comment on “Log or linear? Distinct intuitions of the number scale in Western and Amazonian indigene cultures.” Science 323:38; author reply 38. Available at http://www.sciencemag.org/content/323/5910/38.2.full.

Cantlon JF, Libertus ME, Pinel P, Dehaene S, Brannon EM, Pelphrey KA (2009b) The neural development of an abstract concept of number. J Cogn Neurosci 21:2217–2229.

Cantlon JF, Platt ML, Brannon EM (2009c) Beyond the number domain. Trends Cogn Sci 13:83–91.

Cappelletti M, Butterworth B, Kopelman M (2001) Spared numerical abilities in a case of semantic dementia. Neuropsychologia 39:1224–1239.

Carey M, Burhans DE, Nelson DA (1994) Field sparrow. Birds North Am 103:1–19.

Carlson BA, Hasan SM, Hollmann M, Miller DB, Harmon LJ, Arnegard ME (2011) Brain evolution triggers increased diversification of electric fishes. Science 332:583–586.

Carlson MR, Zhang B, Fang Z, Mischel PS, Horvath S, Nelson SF (2006) Gene connectivity, function, and sequence conservation: Predictions from modular yeast co-expression networks. BMC Genomics 7:40.

Carmichael ST, Price JL (1995) Sensory and premotor connections of the orbital and medial prefrontal cortex of macaque monkeys. J Comp Neurol 363:642–664.

Carmody RN, Wrangham RW (2009) The energetic significance of cooking. J Hum Evol 57: 379–391.

Carmody RN, Weintraub GS, Wrangham RW (2011) Energetic consequences of thermal and nonthermal food processing. Proc Natl Acad Sci USA 108:19199–19203.

Carpenter RHS, ed (1988) Movements of the Eyes (Pion Limited, London).

Carr CE, Konishi M (1990) A circuit for detection of interaural time differences in the brain stem of the barn owl. J Neurosci 10:3227–3246.

Carroll SB, Grenier JK, Weatherbee SD (2005) From DNA to Diversity: Molecular Genetics and the Evolution of Animal Design (Blackwell, Oxford), 2nd Ed.

Carson RJ, Spicer GS (2003) A phylogenetic analysis of the emberizid sparrows based on three mitochondrial genes. Mol Phylogenet Evol 29:43–57.

Casagrande VA, Kaas JH (1994) The afferent, intrinsic, and efferent connections of primary visual cortex in primates. In Cerebral Cortex, eds Peters A, Rockland K (Plenum Press, New York), pp 201–259.

Castilla EE, Lugarinho da Fonseca R, da Graca Dutra M, Bermejo E, Cuevas L, Martínez-Frías ML (1996) Epidemiological analysis of rare polydactylies. Am J Med Genet 65:295–303.

Castro P, Huber ME (1992) Marine Biology (Mosby, St. Louis).

Catania KC (2000a) Cortical-organization in moles: Evidence of new areas and a specialized S2. Somatosens Mot Res 17:335–347.

Catania KC (2000b) Epidermal sensory organs of moles, shrew moles, and desmans: A study of the family Talpidae with comments on the function and evolution of Eimer’s organ. Brain Behav Evol 56:146–174.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Catania KC (2009) Tentacled snakes turn C-starts to their advantage and predict future prey behavior. Proc Natl Acad Sci USA 106:11183–11187.

Catania KC (2010) Born knowing: Tentacled snakes innately predict future prey behavior. PLoS One 5:e10953.

Catania KC (2011) The sense of touch in the star-nosed mole: From mechanoreceptors to the brain. Philos Trans R Soc Lond B Biol Sci 366:3016–3025.

Catania KC (2012) Evolution of brains and behavior for optimal foraging: A tale of two predators. Proc Natl Acad Sci USA 109(Suppl 1):10701-10708.

Catania KC, Kaas JH (1995) Organization of the somatosensory cortex of the star-nosed mole. J Comp Neurol 351:549–567.

Catania KC, Kaas JH (1996) The unusual nose and brain of the star-nosed mole. BioScience 46:578–586.

Catania KC, Kaas JH (1997) Somatosensory fovea in the star-nosed mole: Behavioral use of the star in relation to innervation patterns and cortical representation. J Comp Neurol 387:215–233.

Catania KC, Kaas JH (2001) Areal and callosal connections in the somatosensory cortex of the star-nosed mole. Somatosens Mot Res 18:303–311.

Catania KC, Remple FE (2004) Tactile foveation in the star-nosed mole. Brain Behav Evol 63:1–12.

Catania KC, Remple FE (2005) Asymptotic prey profitability drives star-nosed moles to the foraging speed limit. Nature 433:519–522.

Catania KC, Northcutt RG, Kaas JH (1999) The development of a biological novelty: A different way to make appendages as revealed in the snout of the star-nosed mole Condylura cristata. J Exp Biol 202:2719–2726.

Catania KC, Leitch DB, Gauthier D (2010) Function of the appendages in tentacled snakes (Erpeton tentaculatus). J Exp Biol 213:359–367.

Catania KC, Leitch DB, Gauthier D (2011) A star in the brainstem reveals the first step of cortical magnification. PLoS One 6:e22406.

Chabot N, Chabot N, Charbonneau V, Laramée ME, Tremblay R, Boire D, Bronchti G (2008) Subcortical auditory input to the primary visual cortex in anophthalmic mice. Neurosci Lett 433:129–134.

Chafee MV, Goldman-Rakic PS (1998) Matching patterns of activity in primate prefrontal area 8a and parietal area 7ip neurons during a spatial working memory task. J Neurophysiol 79:2919–2940.

Chagnaud BP, Baker R, Bass AH (2011) Vocalization frequency and duration are coded in separate hindbrain nuclei. Nat Commun 2:346.

Chagnaud BP, Zee MC, Baker R, Bass AH (2012) Innovations in motoneuron synchrony drive rapid temporal modulations in vertebrate acoustic signaling. J Neurophysiol, doi:10.1152/jn.00030.2012.

Chanda B, Bezanilla F (2002) Tracking voltage-dependent conformational changes in skeletal muscle sodium channel during activation. J Gen Physiol 120:629–645.

Chanda B, Asamoah OK, Bezanilla F (2004) Coupling interactions between voltage sensors of the sodium channel as revealed by site-specific measurements. J Gen Physiol 123:217–230.

Changizi MA (2001) Principles underlying mammalian neocortical scaling. Biol Cybern 84: 207–215.

Changizi MA, Zhang Q, Ye H, Shimojo S (2006) The structures of letters and symbols throughout human history are selected to match those found in objects in natural scenes. Am Nat 167:E117–E139.

Charlier TD, Ball GF, Balthazart J (2005) Sexual behavior activates the expression of the immediate early genes c-fos and Zenk (egr-1) in catecholaminergic neurons of male Japanese quail. Neuroscience 131:13–30.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Charvet CJ, Striedter GF (2008) Developmental species differences in brain cell cycle rates between northern bobwhite quail (Colinus virginianus) and parakeets (Melopsittacus undulatus): Implications for mosaic brain evolution. Brain Behav Evol 72:295–306.

Charvet CJ, Striedter GF (2009) Developmental origins of mosaic brain evolution: Morphometric analysis of the developing zebra finch brain. J Comp Neurol 514:203–213.

Charvet CJ, Striedter GF, Finlay BL (2011) Evo-devo and brain scaling: Candidate developmental mechanisms for variation and constancy in vertebrate brain evolution. Brain Behav Evol 78:248–257.

Chase R (2002) Behavior and Its Neural Control in Gastropod Molluscs (Oxford Univ Press, New York).

Chater N, Tenenbaum JB, Yuille A (2006) Probabilistic models of cognition: Conceptual foundations. Trends Cogn Sci 10:287–291.

Chavis DA, Pandya DN (1976) Further observations on corticofrontal connections in the rhesus monkey. Brain Res 117:369–386.

Chen CH, Cretekos CJ, Rasweiler JJ, 4th, Behringer RR (2005) Hoxd13 expression in the developing limbs of the short-tailed fruit bat, Carollia perspicillata. Evol Dev 7:130–141.

Chen J-Y, Dzik J, Edgecombe GD, Ramsköld L, Zhou G-Q (1995) A possible Early Cambrian chordate. Nature 377:720–722.

Chen J, Cheng Y, Iten HV, eds (1997) The Cambrian Explosion and the Fossil Record (National Museum of Natural Science, Taichung, Taiwan).

Chen J-Y, Huang D-Y, Li C-W (1999) An early Cambrian craniate-like chordate. Nature 402:518–522.

Chen J-Y, Oliveri P, Li CW, Zhou GQ, Gao F, Hagadorn JW, Peterson KJ, Davidson EH (2000) Precambrian animal diversity: Putative phosphatized embryos from the Doushantuo Formation of China. Proc Natl Acad Sci USA 97:4457–4462.

Chen J-Y, Huang D-Y, Peng Q-Q, Chi H-M, Wang X-Q, Feng M (2003) The first tunicate from the Early Cambrian of South China. Proc Natl Acad Sci USA 100:8314–8318.

Chen J-Y, Bottjer DJ, Oliveri P, Dornbos SQ, Gao F, Ruffins S, Chi H, Li CW, Davidson EH (2004a) Small bilaterian fossils from 40 to 55 million years before the Cambrian. Science 305:218–222.

Chen J-Y, Oliveri P, Davidson E, Bottjer DJ (2004b) Response to comment on “Small bilaterian fossils from 40 to 55 million years before the Cambrian.” Science 306:1291b.

Chen J-Y, Bottjer DJ, Li G, Hadfield MG, Gao F, Cameron AR, Zhang CY, Xian DC, Tafforeau P, Liao X, Yin ZJ (2009) Complex embryos displaying bilaterian characters from Precambrian Doushantuo phosphate deposits, Weng’an, Guizhou, China. Proc Natl Acad Sci USA 106:19056–19060.

Cheney DL, Seyfarth RM (2007) Baboon Metaphysics: The Evolution of a Social Mind (Univ Chicago Press, Chicago).

Chenn A, Walsh CA (2002) Regulation of cerebral cortical size by control of cell cycle exit in neural precursors. Science 297:365–369.

Chimpanzee Sequencing and Analysis Consortium (2005) Initial sequence of the chimpanzee genome and comparison with the human genome. Nature 437:69–87.

Christiansen MH, Kirby S (2003) Language evolution: Consensus and controversies. Trends Cogn Sci 7:300–307.

Chu-LaGraff Q, Doe CQ (1993) Neuroblast specification and formation regulated by wingless in the Drosophila CNS. Science 261:1594–1597.

Cipolotti L, Butterworth B, Denes G (1991) A specific deficit for numbers in a case of dense acalculia. Brain 114:2619–2637.

Clancy B, Darlington RB, Finlay BL (2000) The course of human events: Predicting the timing of primate neural development. Dev Sci 3:57–66.

Clancy B, Darlington RB, Finlay BL (2001) Translating developmental time across mammalian species. Neuroscience 105:7–17.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Clancy B, Kersh B, Hyde J, Darlington RB, Anand KJ, Finlay BL (2007) Web-based method for translating neurodevelopment from laboratory species to humans. Neuroinformatics 5:79–94.

Clark AG, Glanowski S, Nielsen R, Thomas PD, Kejariwal A, Todd MA, Tanenbaum DM, Civello D, Lu F, Murphy B, Ferriera S, Wang G, Zheng X, White TJ, Sninsky JJ, Adams MD, Cargill M (2003) Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios. Science 302:1960–1963.

Clark DA, Mitra PP, Wang SS (2001) Scalable architecture in mammalian brains. Nature 411:189–193.

Cline HT, Debski EA, Constantine-Paton M (1987) N-methyl-d-aspartate receptor antagonist desegregates eye-specific stripes. Proc Natl Acad Sci USA 84:4342–4345.

Coates M (2003) The evolution of paired fins. Theory Biosci 122:266–287.

Cockerell TDA (1901) Three new nudibranchs from California. J Malacol 8:85–87.

Cohen L, Dehaene S (2004) Specialization within the ventral stream: The case for the visual word form area. Neuroimage 22:466–476.

Cohen MJ, Winn HE (1967) Electrophysiological observations on hearing and sound production in the fish, Porichthys notatus. J Exp Zool 165:355–369.

Cohen SM, Jürgens G (1990) Mediation of Drosophila head development by gap-like segmentation genes. Nature 346:482–485.

Cohen YE, Russ BE, Davis SJ, Baker AE, Ackelson AL, Nitecki R (2009) A functional role for the ventrolateral prefrontal cortex in non-spatial auditory cognition. Proc Natl Acad Sci USA 106:20045–20050.

Cohen Kadosh R, Cohen Kadosh K, Kaas A, Henik A, Goebel R (2007) Notation-dependent and independent representations of numbers in the parietal lobes. Neuron 53:307–314.

Cohen Kadosh R, Cohen Kadosh K, Henik A (2008) When brightness counts: The neuronal correlate of numerical-luminance interference. Cereb Cortex 18:337–343.

Collingwood C (1879) Scyllea pelagica, specimens from China Sea, and spawn described. Trans Linn Soc Lond 2:137–138.

Conaco C, Bassett DS, Zhou H, Arcila ML, Degnan SM, Degnan BM, Kosik KS (2012) Functionalization of a protosynaptic gene expression network. Proc Natl Acad Sci USA 109(Suppl 1):10612-10618.

Conover MR (2007) Predator-Prey Dynamics: The Role of Olfaction (CRC, Boca Raton, FL), p 248.

Conroy GC (1990) Primate Evolution (WW Norton, New York).

Constantine-Paton M, Law MI (1978) Eye-specific termination bands in tecta of three-eyed frogs. Science 202:639–641.

Conway Morris S (1986) The community structure of the Middle Cambrian Phyllopod Bed (Burgess Shale). Palaeontology 29:423–467.

Conway Morris S (1993) Ediacaran-like fossils in Cambrian Burgess Shale-type faunas of North America. Palaeontology 36:593–635.

Conway Morris S (1998) The Crucible of Creation (Oxford University Press, Oxford).

Conway Morris S (2000a) Evolution: Bringing molecules into the fold. Cell 100:1–11.

Conway Morris S (2000b) The Cambrian “explosion”: Slow-fuse or megatonnage? Proc Natl Acad Sci USA 97:4426–4429.

Cooke DF, Taylor CS, Moore T, Graziano MSA (2003) Complex movements evoked by microstimulation of the ventral intraparietal area. Proc Natl Acad Sci USA 100:6163–6168.

Cooke DF, Padberg J, Zahner T, Krubitzer L (2011) The functional organization and cortical connections of motor cortex in squirrels. Cereb Cortex 22:1959–1978.

Cooper HM, Herbin M, Nevo E (1993) Visual system of a naturally microphthalmic mammal: The blind mole rat, Spalax ehrenbergi. J Comp Neurol 328:313–350.

Cooper LN, Berta A, Dawson SD, Reidenberg JS (2007) Evolution of hyperphalangy and digit reduction in the cetacean manus. Anat Rec (Hoboken) 290:654–672.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Cornellissen T (1970) Erpeton tentaculatum, een vissende slang. Lacerta 28:88–92.

Corning WC, Dyal JA, Willows AOD (1973) Invertebrate Learning: Protozoans Through Annelids (Plenum Press, New York).

Cosans C (1994) Anatomy, metaphysics, and values: The ape brain debate reconsidered. Biol Philos 9:129–165.

Costa SS, Andrade R, Carneiro LA, Gonçalves EJ, Kotrschal K, Oliveira RF (2011) Sex differences in the dorsolateral telencephalon correlate with home range size in blenniid fish. Brain Behav Evol 77:55–64.

Coudé G, Ferrari PF, Rodà F, Maranesi M, Borelli E, Veroni V, Monti F, Rozzi S, Fogassi L (2011) Neurons controlling voluntary vocalization in the macaque ventral premotor cortex. PLoS ONE 6:e26822.

Cragg BG (1967) The density of synapses and neurones in the motor and visual areas of the cerebral cortex. J Anat 101:639–654.

Cretekos CJ, Rasweiler JJ, Behringer RR (2001) Comparative studies on limb morphogenesis in mice and bats: A functional genetic approach towards a molecular understanding of diversity in organ formation. Reprod Fertil Dev 13:691–695.

Cretekos CJ, Deng JM, Green ED, Rasweiler JJ, Behringer RR; NISC Comparative Sequencing Program (2007) Isolation, genomic structure and developmental expression of Fgf8 in the short-tailed fruit bat, Carollia perspicillata. Int J Dev Biol 51:333–338.

Crick F, Jones E (1993) Backwardness of human neuroanatomy. Nature 361:109–110.

Croll RP (1987) Identified neurons and cellular homologies. In Nervous Systems in Invertebrates, ed Ali MA (Plenum Press, New York), pp 41–59.

Cross DJ, Minoshima S, Nishimura S, Noda A, Tsukada H, Kuhl DE (2000) Three-dimensional stereotactic surface projection analysis of macaque brain PET: Development and initial applications. J Nucl Med 41:1879–1887.

Crossland WJ, Cowan WM, Rogers LA (1975) Studies on the development of the chick optic tectum. IV. An autoradiographic study of the development of retino-tectal connections. Brain Res 91:1–23.

Curley JP, Davidson S, Bateson P, Champagne FA (2009) Social enrichment during postnatal development induces transgenerational effects on emotional and reproductive behavior in mice. Front Behav Neurosci 3:25.

Curley JP, Jensen CL, Franks B, Champagne FA (2012) Variation in maternal and anxiety-like behavior associated with discrete patterns of oxytocin and vasopressin 1a receptor density in the lateral septum. Horm Behav 61:454–461.

Cusick CG, Kaas JH (1988) Cortical connections of area 18 and dorsolateral visual cortex in squirrel monkeys. Vis Neurosci 1:211–237.

da Costa NM, Martin KAC (2010) Whose cortical columns would that be? Front Neuroanat 4:1–10.

Daeschler EB, Shubin NH, Jenkins FA, Jr (2006) A Devonian tetrapod-like fish and the evolution of the tetrapod body plan. Nature 440:757–763.

Danon L, Diaz-Guilera A, Duch J, Arenas A (2005) Comparing community structure identification. J Stat Mech 2005:P09008.

Darwin C (1859) On the Origin of Species by Means of Natural Selection (John Murray, London).

Darwin C (1871) The Descent of Man, and Selection in Relation to Sex (John Murray, London).

Darwin C (1876) The Origin of Species by Natural Selection, or the Preservation of Favoured Races in the Struggle for Life (John Murray, London).

Dasen JS, Liu J-P, Jessell TM (2003) Motor neuron columnar fate imposed by sequential phases of Hox-c activity. Nature 425:926–933.

Davidson EH (2006) The Regulatory Genome (Academic Press, San Diego).

Davies NB (1976) Food, flocking and territorial behaviour of pied wagtails (Motacilla alba yarrellii Gould) in winter. J Anim Ecol 45:235–253.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Davies TG, Field LM, Usherwood PN, Williamson MS (2007) DDT, pyrethrins, pyrethroids and insect sodium channels. IUBMB Life 59:151–162.

Davis JL, Eichenbaum H, eds (1991) Olfaction: A Model System for Computational Neuroscience (MIT Press, Cambridge, MA).

Davis WJ, Mpitsos GJ (1971) Behavioral choice and habituation in the marine mollusk Pleurobranchaea californica MacFarland (Gastropoda, Opisthobranchia). Z Vgl Physiol 75:207–232.

Dawkins R (1978) Replicator selection and the extended phenotype. Z Tierpsychol 47:61–76.

Dawkins R (1982) The Extended Phenotype (Oxford Univ Press, Oxford).

Dawson DR, Killackey HP (1987) The organization and mutability of the forepaw and hindpaw representations in the somatosensory cortex of the neonatal rat. J Comp Neurol 256:246–256.

Day LB, Crews D, Wilczynski W (1999) Relative medial and dorsal cortex volume in relation to foraging ecology in congeneric lizards. Brain Behav Evol 54:314–322.

De Carlos JA, Borrell J (2007) A historical reflection of the contributions of Cajal and Golgi to the foundations of neuroscience. Brain Res Rev 55:8–16.

de Hevia MD, Spelke ES (2009) Spontaneous mapping of number and space in adults and young children. Cognition 110:198–207.

de Hevia MD, Spelke ES (2010) Number-space mapping in human infants. Psychol Sci 21: 653–660.

De Queiroz A, Wimberger PH (1993) The usefulness of behavior for phylogeny estimation: Levels of homoplasy in behavioral and morphological characters. Evolution 47:46–60.

De Robertis EM, Sasai Y (1996) A common plan for dorsoventral patterning in Bilateria. Nature 380:37–40.

De Sousa A, Woods B (2007) The hominin fossil record and the emergence of the modern human central nervous system. In Evolution of Nervous Systems, ed Kaas J (Elsevier, Oxford), Vol 4, pp 291–336.

De Vries GJ, Buijs RM (1983) The origin of the vasopressinergic and oxytocinergic innervation of the rat brain with special reference to the lateral septum. Brain Res 273:307–317.

De Vries GJ, Panzica GC (2006) Sexual differentiation of central vasopressin and vasotocin systems in vertebrates: Different mechanisms, similar endpoints. Neuroscience 138:947–955.

Deacon TW (1992) Cortical connections of the inferior arcuate sulcus cortex in the macaque brain. Brain Res 573:8–26.

Deacon TW (1997a) The Symbolic Species: The Co-Evolution of Language and the Brain (W.W. Norton, New York), 1st Ed.

Deacon TW (1997b) What makes the human brain different? Annu Rev Anthropol 26:337–357.

Deaner RO, Isler K, Burkart J, van Schaik C (2007) Overall brain size, and not encephalization quotient, best predicts cognitive ability across non-human primates. Brain Behav Evol 70:115–124.

DeBose JL, Nevitt GA (2008) The use of odors at different spatial scales: Comparing birds with fish. J Chem Ecol 34:867–881.

DeFelipe J, Alonso-Nanclares L, Arellano JI (2002) Microstructure of the neocortex: Comparative aspects. J Neurocytol 31:299–316.

Dehaene S (1992) Varieties of numerical abilities. Cognition 44:1–42.

Dehaene S (2009) Reading in the Brain (Viking, New York).

Dehaene S, Cohen L (2007) Cultural recycling of cortical maps. Neuron 56:384–398.

Dehaene S, Piazza M, Pinel P, Cohen L (2003) Three parietal circuits for number processing. Cogn Neuropsychol 20:487–506.

Dehaene S, Izard V, Spelke E, Pica P (2008) Log or linear? Distinct intuitions of the number scale in Western and Amazonian indigene cultures. Science 320:1217–1220.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Dehnhardt G, Mauck B (2008) Mechanoreception in secondarily aquatic vertebrates. In Sensory Evolution on the Threshold: Adaptations in Secondarily Aquatic Vertebrates, eds Thewissen JGM, Nummela S (Univ California Press, Berkeley), pp 295–314.

Delcomyn F (1980) Neural basis of rhythmic behavior in animals. Science 210:492–498.

Delgado A, Alonso A, Damas C, Trujillo CM (2005) The midbrain of sauropsides shares a common subdivision pattern defined by embryonic radial glia. Brain Res Bull 66: 479–483.

Deloulme JC, Gensburger C, Sarhan S, Seiler N, Sensenbrenner M (1991) Effects of basic fibroblast growth factor on the development of GABAergic neurons in culture. Neuroscience 42:561–568.

Demb JB, Desmond JE, Wagner AD, Vaidya CJ, Glover GH, Gabrieli JD. (1995) Semantic encoding and retrieval in the left inferior prefrontal cortex: A functional MRI study of task difficulty and process specificity. J Neurosci 15:5870–5878.

Démonet JF, Chollet F, Ramsay S, Cardebat D, Nespoulous JL, Wise R, Rascol A, Frackowiak R (1992) The anatomy of phonological and semantic processing in normal subjects. Brain 115:1753–1768.

Denes AS, Jékely G, Steinmetz PR, Raible F, Snyman H, Prud’homme B, Ferrier DE, Balavoine G, Arendt D (2007) Molecular architecture of annelid nerve cord supports common origin of nervous system centralization in Bilateria. Cell 129:277–288.

Derby CD (2007) Why have neurogenesis in adult olfactory systems? The Presidential Symposium at the 2006 AChemS Conference. Chem Senses 32:361–363.

Deschênes M, Veinante P, Zhang ZW (1998) The organization of corticothalamic projections: Reciprocity versus parity. Brain Res Brain Res Rev 28:286–308.

Desmond A (1994) Huxley: From Devil’s Disciple to Evolution’s High Priest (Addison-Wesley, Reading, MA).

Desmond ME, Levitan ML, Haas AR (2005) Internal luminal pressure during early chick embryonic brain growth: Descriptive and empirical observations. Anat Rec A Discov Mol Cell Evol Biol 285:737–747.

Diester I, Nieder A (2007) Semantic associations between signs and numerical categories in the prefrontal cortex. PLoS Biol 5:e294.

Dinapoli A, Klussmann-Kolb A (2010) The long way to diversity—phylogeny and evolution of the Heterobranchia (Mollusca:Gastropoda). Mol Phylogenet Evol 55:60–76.

Dobzhansky TG, Ayala FJ, Stebbins GL, Valentine JW (1977) Evolution (Freeman, San Francisco).

Doe CQ, Goodman CS (1985) Early events in insect neurogenesis. I. Development and segmental differences in the pattern of neuronal precursor cells. Dev Biol 111:193–205.

Domazet-Lošo T, Tautz D (2010) A phylogenetically based transcriptome age index mirrors ontogenetic divergence patterns. Nature 468:815–818.

Donoghue JP, Leibovic S, Sanes JN (1992) Organization of the forelimb area in squirrel monkey motor cortex: Representation of digit, wrist, and elbow muscles. Exp Brain Res 89:1–19.

Donoghue PCJ, Purnell MA (2009) Distinguishing heat from light in debate over controversial fossils. Bioessays 31:178–189.

Donovan DA, Pennings SC, Carefoot TH (2006) Swimming in the sea hare Aplysia brasiliana: Cost of transport, parapodial morphometry, and swimming behavior. J Exp Mar Biol Ecol 328:76–86.

Doron N, Wollberg Z (1994) Cross-modal neuroplasticity in the blind mole rat Spalax ehrenbergi: A WGA-HRP tracing study. Neuroreport 5:2697–2701.

Dorsett DA, Willows AOD, Hoyle G (1969) Centrally generated nerve impulse sequences determining swimming behavior in Tritonia. Nature 224:711–712.

Dorus S, Vallender EJ, Evans PD, Anderson JR, Gilbert SL, Mahowald M, Wyckoff GJ, Malcom CM, Lahn BT (2004) Accelerated evolution of nervous system genes in the origin of Homo sapiens. Cell 119:1027–1040.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Dougherty RF, Koch VM, Brewer AA, Fischer B, Modersitzki J, Wandell BA (2003) Visual field representations and locations of visual areas V1/2/3 in human visual cortex. J Vis 3:586–598.

Douzery EJP, Snell EA, Bapteste E, Delsuc F, Philippe H (2004) The timing of eukaryotic evolution: Does a relaxed molecular clock reconcile proteins and fossils? Proc Natl Acad Sci USA 101:15386–15391.

Dove H, Stollewerk A (2003) Comparative analysis of neurogenesis in the myriapod Glomeris marginata (Diplopoda) suggests more similarities to chelicerates than to insects. Development 130:2161–2171.

Downing PE, Jiang Y, Shuman M, Kanwisher N (2001) A cortical area selective for visual processing of the human body. Science 293:2470–2473.

Drew T, Dubuc R, Rossignol S (1986) Discharge patterns of reticulospinal and other reticular neurons in chronic, unrestrained cats walking on a treadmill. J Neurophysiol 55:375–401.

Driver J, Noesselt T (2008) Multisensory interplay reveals crossmodal influences on “sensory-specific” brain regions, neural responses, and judgments. Neuron 57:11–23.

Duboué ER, Keene AC, Borowsky RL (2011) Evolutionary convergence on sleep loss in cavefish populations. Curr Biol 21:671–676.

Duchaine BC, Yovel G, Butterworth EJ, Nakayama K (2006) Prosopagnosia as an impairment to face-specific mechanisms: Elimination of the alternative hypotheses in a developmental case. Cogn Neuropsychol 23:714–747.

Dudzinski KM, Gregg JD, Ribic CA, Kuczaj SA (2009) A comparison of pectoral fin contact between two different wild dolphin populations. Behav Processes 80:182–190.

Duellman WE, Trueb L (1986) Biology of Amphibians (Johns Hopkins Univ Press, Baltimore, MD).

Dulai KS, von Dornum M, Mollon JD, Hunt DM (1999) The evolution of trichromatic color vision by opsin gene duplication in New World and Old World primates. Genome Res 9:629–638.

Duman-Scheel M, Patel NH (1999) Analysis of molecular marker expression reveals neuronal homology in distantly related arthropods. Development 126:2327–2334.

Duman-Scheel M, Li X, Orlov I, Noll M, Patel NH (1997) Genetic separation of the neural and cuticular patterning functions of gooseberry. Development 124:2855–2865.

Dusenbery DB (1992) Sensory Ecology (W.H. Freeman, New York).

Dzik J (1995) Yunnanozoon and the ancestry of chordates. Acta Palaeontol Pol 40:341–360.

Eaton RC, Hackett JT (1984) The role of Mauthner cell in fast-starts involving escapes in teleost fishes. In Neural Mechanisms of Startle Behavior, ed Eaton RC (Plenum Press, New York), pp 213–266.

Economides JR, Sincich LC, Adams DL, Horton JC (2011) Orientation tuning of cytochrome oxidase patches in macaque primary visual cortex. Nat Neurosci 14:1574–1580.

Edgecombe GD, Giribet G, Dunn CW, Hejnol A, Kristensen RM, Neves RC, Rouse GW, Worsaae K, Sørensen MV (2011) Higher-level metazoan relationships: Recent progress and remaining questions. Org Divers Evol 11:151–172.

Edmunds M (1968) On the swimming and defensive response of Hexabranchus marginatus (Mollusca, Nudibranchia). J. Linnean Soc 47:425–429.

Eifuku S, De Souza WC, Tamura R, Nishijo H, Ono T (2004) Neuronal correlates of face identification in the monkey anterior temporal cortical areas. J Neurophysiol 91:358–371.

Eimer T (1871) Die Schnautze des Maulwurfs als Tastwerkzeug. Arch Mikr Anat 7:181–191.

Eisen MB, Spellman PT, Brown PO, Botstein D (1998) Cluster analysis and display of genome-wide expression patterns. Proc Natl Acad Sci USA 95:14863–14868.

Eisthen HL (2002) Why are olfactory systems of different animals so similar? Brain Behav Evol 59:273–293.

Ellis W (1999a) Plocamopherus imperialis Angas, 1864. Aust Nudibranch News 11:1–4.

Ellis W (1999b) Plocamopherus tilesii Bergh, 1877. Aust Nudibranch News 2:1–4.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Elman JL, Bates EA, Johnson MH, Karmiloff-Smith A, Parisi D, Plunkett K (1996) Rethinking Innateness: A Connectionist Perspective on Development (MIT Press, Cambridge, MA).

Emerson RW, Cantlon JF (2012) Early math achievement and functional connectivity in the fronto-parietal network. Dev Cogn Neurosci 2:S139–S151.

Emmerton J (2001) Birds’ judgments of number and quantity. In Avian Visual Cognition, ed Cook RG. Available at http://www.pigeon.psy.tufts.edu/avc/emmerton/. Accessed April 1, 2012.

Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Pääbo S (2002) Molecular evolution of FOXP2, a gene involved in speech and language. Nature 418: 869–872.

Enard W, Gehre S, Hammerschmidt K, Hölter SM, Blass T, Somel M, Brückner MK, Schreiweis C, Winter C, Sohr R, Becker L, Wiebe V, Nickel B, Giger T, Müller U, Groszer M, Adler T, Aguilar A, Bolle I, Calzada-Wack J, Dalke C, Ehrhardt N, Favor J, Fuchs H, Gailus-Durner V, Hans W, Hölzlwimmer G, Javaheri A, Kalaydjiev S, Kallnik M, Kling E, Kunder S, Mossbrugger I, Naton B, Racz I, Rathkolb B, Rozman J, Schrewe A, Busch DH, Graw J, Ivandic B, Klingenspor M, Klopstock T, Ollert M, Quintanilla-Martinez L, Schulz H, Wolf E, Wurst W, Zimmer A, Fisher SE, Morgenstern R, Arendt T, de Angelis MH, Fischer J, Schwarz J, Pääbo S (2009) A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell 137:961–971.

Epstein R, Kanwisher N (1998) A cortical representation of the local visual environment. Nature 392:598–601.

Erwin DH (2006) The developmental origins of animal bodyplans. In Neoproterozoic Geobiology and Paleobiology, eds Xiao S, Kaufman AJ (Springer, Berlin), pp 159–197.

Erwin DH, Laflamme M, Tweedt SM, Sperling EA, Pisani D, Peterson KJ (2011) The Cambrian conundrum: Early divergence and later ecological success in the early history of animals. Science 334:1091–1097.

Erzurumlu RS, Kind PC (2001) Neural activity: Sculptor of “barrels” in the neocortex. Trends Neurosci 24:589–595.

Evans N, Levinson SC (2009) The myth of language universals: Language diversity and its importance for cognitive science. Behav Brain Sci 32:429–448.

Evans PD, Gilbert SL, Mekel-Bobrov N, Vallender EJ, Anderson JR, Vaez-Azizi LM, Tishkoff SA, Hudson RR, Lahn BT (2005) Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans. Science 309:1717–1720.

Faber DS, Fetcho JR, Korn H (1989) Neuronal networks underlying the escape response in goldfish. General implications for motor control. Ann N Y Acad Sci 563:11–33.

Fahey B, Degnan BM (2010) Origin of animal epithelia: Insights from the sponge genome. Evol Dev 12:601–617.

Farmer WM (1970) Swimming gastropods (Opisthobranchia and Prosobranchia). Veliger 13:73–89.

Fedonkin MA, Waggoner BM (1997) The Late Precambrian fossil Kimberella is a mollusc-like bilaterian organism. Nature 388:868–871.

Fedonkin MA, Gehling JG, Grey K, Narbonne GM, Vickers-Rich P (2007) The Rise of Animals (Johns Hopkins Univ Press, Baltimore, MD).

Feenders G, Liedvogel M, Rivas M, Zapka M, Horita H, Hara E, Wada K, Mouritsen H, Jarvis ED (2008) Molecular mapping of movement-associated areas in the avian brain: A motor theory for vocal learning origin. PLoS ONE 3:e1768.

Feigenson L (2007) The equality of quantity. Trends Cogn Sci 11:185–187.

Feigenson L, Dehaene S, Spelke E (2004) Core systems of number. Trends Cogn Sci 8:307–314.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Feldman CR, Brodie ED, Jr, Brodie ED, 3rd, Pfrender ME (2009) The evolutionary origins of beneficial alleles during the repeated adaptation of garter snakes to deadly prey. Proc Natl Acad Sci USA 106:13415–13420.

Feldman CR, Brodie ED, Jr, Brodie ED, 3rd, Pfrender ME (2012) Constraint shapes convergence in tetrodotoxin-resistant sodium channels of snakes. Proc Natl Acad Sci USA 109:4556–4561.

Felleman DJ (2008) Functional maps in visual cortex: Topographic, modular, and column organizations. In The Senses, eds Masland RH, Albright TA (Elsevier, London), pp 577–593.

Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA (2003) Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. J Comp Neurol 460:266–279.

Ferreira A, Bertsch H (1972) Additional data on Flabellina telja (Gastropoda: Opisthobranchia). Veliger 14:414–415.

Ferrier D, ed (1886) The Functions of the Brain (Putnam Press, New York; reprinted 1978 by University Publications of America, Washington DC).

Fine ML, Ladich F (2003) Sound production, spine locking, and related adaptations. In Catfishes, eds Arratia G, Kapoor BG, Chardon M, Diogo R (Science Publishers, Enfield, NH), Vol 1, pp 249–290.

Fine ML, Friel JP, McElroy D, King CB, Loesser KE, Newton S (1997) Pectoral spine locking and sound production in the channel catfish Ictalurus punctatus. Copeia 4:777–790.

Finlay BL, Darlington RB (1995) Linked regularities in the development and evolution of mammalian brains. Science 268:1578–1584.

Finlay BL, Darlington RB, Nicastro N (2001) Developmental structure in brain evolution. Behav Brain Sci 24:263–278.

Finlay BL, Hinz F, Darlington RB (2011) Mapping behavioural evolution onto brain evolution: The strategic roles of conserved organization in individuals and species. Philos Trans R Soc Lond B Biol Sci 366:2111–2123.

Finnerty JR, Martindale MQ (1998) The evolution of the Hox cluster: Insights from outgroups. Curr Opin Genet Dev 8:681–687.

Finnigan GC, Hanson-Smith V, Stevens TH, Thornton JW (2012) Evolution of increased complexity in a molecular machine. Nature 481:360–364.

Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME (1998) Localisation of a gene implicated in a severe speech and language disorder. Nat Genet 18:168–170.

Fitch WM (1970) Distinguishing homologous from analogous proteins. Syst Zool 19:99–113.

Fitzpatrick D (1996) The functional organization of local circuits in visual cortex: Insights from the study of tree shrew striate cortex. Cereb Cortex 6:329–341.

Flachsenberger W, Kerr DIB (1985) Lack of effect of tetrodotoxin and of an extract from the posterior salivary gland of the blue-ringed octopus following injection into the octopus and following application to its brachial nerve. Toxicon 23:997–999.

Florence SL, Kaas JH (1992) Ocular dominance columns in area 17 of Old World macaque and talapoin monkeys: Complete reconstructions and quantitative analyses. Vis Neurosci 8:449–462.

Fodor J (1983) The Modularity of Mind (MIT Press, Cambridge, MA).

Forey P, Janvier P (1993) Agnathans and the origin of jawed vertebrates. Nature 361:129–134.

Fortunato S, Barthélemy M (2007) Resolution limit in community detection. Proc Natl Acad Sci USA 104:36–41.

Foster SA, Cresko WA, Johnson KP, Tlusty MU, Willmott HE (1996) Patterns of homoplasy in behavioral evolution. In Homoplasy: The Recurrence of Similarity in Evolution, eds Sanderson MJ, Hufford L (Academic Press, San Diego), pp 245–269.

Frahm HD, Stephan H, Stephan M (1982) Comparison of brain structure volumes in Insectivora and Primates. I. Neocortex. J Hirnforsch 23:375–389.

Freake MJ, Muheim R, Phillips JB (2006) Magnetic maps in animals: A theory comes of age? Q Rev Biol 81:327–347.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Frederick DE, Barlas L, Ievins A, Kay LM (2009) A critical test of the overlap hypothesis for odor mixture perception. Behav Neurosci 123:430–437.

Freedman DJ, Miller EK (2008) Neural mechanisms of visual categorization: Insights from neurophysiology. Neurosci Biobehav Rev 32:311–329.

Friederici AD (2009) Pathways to language: Fiber tracts in the human brain. Trends Cogn Sci 13:175–181.

Friedman RM, Chen LM, Roe AW (2004) Modality maps within primate somatosensory cortex. Proc Natl Acad Sci USA 101:12724–12729.

Fu X, Giavalisco P, Liu X, Catchpole G, Fu N, Ning ZB, Guo S, Yan Z, Somel M, Pääbo S, Zeng R, Willmitzer L, Khaitovich P (2011) Rapid metabolic evolution in human prefrontal cortex. Proc Natl Acad Sci USA 108:6181–6186.

Fülleborn F (1894) Bericht über eine zur Untersuchung der Entwickelung von Amia, Lepidosteus und Necturus unternommene Reise nach Nord-America (Sitzungsberichte der Preussischen Akademie der Wissenschaften, Berlin).

Funahashi S, Bruce CJ, Goldman-Rakic PS (1989) Mnemonic coding of visual space in the monkey’s dorsolateral prefrontal cortex. J Neurophysiol 61:1–19.

Funahashi S, Chafee MV, Goldman-Rakic PS (1993) Prefrontal neuronal activity in rhesus monkeys performing a delayed anti-saccade task. Nature 365:753–756.

Gabi M, Collins CE, Wong P, Torres LB, Kaas JH, Herculano-Houzel S (2010) Cellular scaling rules for the brains of an extended number of primate species. Brain Behav Evol 76:32–44.

Gagliardo A, Ioalè P, Savini M, Wild JM (2006) Having the nerve to home: Trigeminal magnetoreceptor versus olfactory mediation of homing in pigeons. J Exp Biol 209: 2888–2892.

Galaburda AM, Pandya DN (1983) The intrinsic architectonic and connectional organization of the superior temporal region of the rhesus monkey. J Comp Neurol 221:169–184.

Galione A, Evans AM, Ma J, Parrington J, Arredouani A, Cheng X, Zhu MX (2009) The acid test: The discovery of two-pore channels (TPCs) as NAADP-gated endolysosomal Ca(2+) release channels. Pflugers Arch 458:869–876.

Gall BG, Brodie ED (2011) Survival and growth of the caddisfly Limnephilus flavastellus after predation on toxic eggs of the rough-skinned newt (Taricha granulosa). Can J Zool 89:483–489.

Gallistel CR (1989) Animal cognition: The representation of space, time and number. Annu Rev Psychol 40:155–189.

Gallistel CR, Gelman R (1992) Preverbal and verbal counting and computation. Cognition 44:43–74.

Gallistel CR, Gelman II (2000) Non-verbal numerical cognition: From reals to integers. Trends Cogn Sci 4:59–65.

Gans C (1973) Sound production in the Salientia: Mechanism and evolution of the emitter. Am Zool 13:1179–1194.

Gans C, Maderson PFA (1973) Sound producing mechanisms in recent reptiles: Review and comment. Am Zool 13:1195–1203.

Gans C, Northcutt RG (1983) Neural crest and the origin of vertebrates: A new head. Science 220:268–273.

Gardiner JM, Atema J (2007) Sharks need the lateral line to locate odor sources: Rheotaxis and eddy chemotaxis. J Exp Biol 210:1925–1934.

Gardiner JM, Atema J (2010) The function of bilateral odor arrival time differences in olfactory orientation of sharks. Curr Biol 20:1187–1191.

Garstang W (1890) A complete list of the opisthobranchiate mollusca found at Plymouth; with further observations on their morphology, colours, and natural history. J Mar Biol Assoc UK (New Ser) 1:399–457.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Gasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown PO (2000) Genomic expression programs in the response of yeast cells to environmental changes. Mol Biol Cell 11:4241–4257.

Gatome CW, Mwangi DK, Lipp HP, Amrein I (2010) Hippocampal neurogenesis and cortical cellular plasticity in Wahlberg’s epauletted fruit bat: A qualitative and quantitative study. Brain Behav Evol 76:116–127.

Gauthier I, Nelson CA (2001) The development of face expertise. Curr Opin Neurobiol 11: 219–224.

Gauthier I, Tarr MJ, Anerson AW, Skudlarski P, Gore JC (1999) Activation of the middle fusiform “face area” increases with expertise in recognizing novel objects. Nat Neurosci 6:568–573.

Gazzaniga MS (2008) Human: The Science Behind What Makes Us Unique (Ecco/Harper Collins, New York).

Geffeney SL, Fujimoto E, Brodie ED, 3rd, Brodie ED, Jr, Ruben PC (2005) Evolutionary diversification of TTX-resistant sodium channels in a predator-prey interaction. Nature 434:759–763.

Gehling JG (1987) Earliest known echinoderm—a new Ediacaran fossil from the Pound Subgroup of South Australia. Alcheringa 11:337–345.

Gehling JG (1991) The case for Ediacaran fossil roots to the metazoan tree. Mem Geol Soc India 20:181–223.

Gelfand JR, Bookheimer SY (2003) Dissociating neural mechanisms of temporal sequencing and processing phonemes. Neuron 38:831–842.

Gelman R, Butterworth B (2005) Number and language: How are they related? Trends Cogn Sci 9:6–10.

Gelman R, Gallistel CR (1978) The Child’s Understanding of Number (Harvard Univ Press, Cambridge, MA), p xiii.

Gentilucci M, Dalla Volta R, Gianelli C (2008) When the hands speak. J Physiol Paris 102: 21–30.

Gentner D, Medina J (1998) Similarity and the development of rules. Cognition 65:263–297.

Geoffroy Saint-Hilaire E (1830) Principes de Philosophie Zoologique (Pichon et Didier, Paris).

Georges-Labouesse E, Mark M, Messaddeq N, Gansmüller A (1998) Essential role of alpha 6 integrins in cortical and retinal lamination. Curr Biol 8:983–986.

Gerbella M, Belmalih A, Borra E, Rozzi S, Luppino G (2010) Cortical connections of the macaque caudal ventrolateral prefrontal areas 45A and 45B. Cereb Cortex 20:141–168.

Getting PA (1977) Neuronal organization of escape swimming in Tritonia. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 121:325–342.

Getting PA (1981) Mechanisms of pattern generation underlying swimming in Tritonia. I. Neuronal network formed by monosynaptic connections. J Neurophysiol 46:65–79.

Getting PA (1983) Neural control of swimming in Tritonia. In Neural Origin of Rhythmic Movements, eds Roberts A, Roberts BL (Cambridge Univ Press, New York), pp 89–128.

Getting PA, Lennard PR, Hume RI (1980) Central pattern generator mediating swimming in Tritonia. I. Identification and synaptic interactions. J Neurophysiol 44:151–164.

Gharbawie OA, Stepniewska I, Kaas JH (2011a) Cortical connections of functional zones in posterior parietal cortex and frontal cortex motor regions in New World monkeys. Cereb Cortex 21:1981–2002.

Gharbawie OA, Stepniewska I, Qi HX, Kaas JH (2011b) Multiple parietal-frontal pathways mediate grasping in macaque monkeys. J Neurosci 31:11660–11677.

Ghazanfar AA, Maier JX, Hoffman KL, Logothetis NK (2005) Multisensory integration of dynamic faces and voices in rhesus monkey auditory cortex. J Neurosci 25:5004–5012.

Gibson E (1969) Principles of Perceptual Learning and Development (Appleton-Century-Crofts, New York), p viii.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Gibson KR (1986) Cognition, brain size, and the extraction of embedded food resources. In Primate Ontogeny, Cognition, and Social Behavior, eds Else JG, Lee PC (Cambridge Univ Press, Cambridge, UK), pp 93–105.

Gibson KR (2002) Evolution of human intelligence: The roles of brain size and mental construction. Brain Behav Evol 59:10–20.

Gifford GW, 3rd, MacLean KA, Hauser MD, Cohen YE (2005) The neurophysiology of functionally meaningful categories: Macaque ventrolateral prefrontal cortex plays a critical role in spontaneous categorization of species-specific vocalizations. J Cogn Neurosci 17:1471–1482.

Gilbert C, McCafferty D, Le Maho Y, Martrette JM, Giroud S, Blanc S, Ancel A (2010) One for all and all for one: The energetic benefits of huddling in endotherms. Biol Rev Camb Philos Soc 85:545–569.

Gilbert SJ, Spengler S, Simons JS, Steele JD, Lawrie SM, Frith CD, Burgess PW (2006) Functional specialization within rostral prefrontal cortex (area 10): A meta-analysis. J Cogn Neurosci 18:932–948.

Gilestro GF, Tononi G, Cirelli C (2009) Widespread changes in synaptic markers as a function of sleep and wakefulness in Drosophila. Science 324:109–112.

Gilland E, Baker R (2005) Evolutionary patterns of cranial nerve efferent nuclei in vertebrates. Brain Behav Evol 66:234–254.

Gillette R, Jing J (2001) The role of the escape swim motor network in the organization of behavioral hierarchy and arousal in Pleurobranchaea. Am Zool 41:983–992.

Gillette R, Saeki M, Huang R-C (1991) Defense mechanisms in notaspid snails: Acid humor and evasiveness. J Exp Biol 156:335–347.

Gilmore CK, McCarthy SE, Spelke ES (2007) Symbolic arithmetic knowledge without instruction. Nature 447:589–591.

Ginsburg S, Jablonka E (2010) The evolution of associative learning: A factor in the Cambrian explosion. J Theor Biol 266:11–20.

Girvan M, Newman MEJ (2002) Community structure in social and biological networks. Proc Natl Acad Sci USA 99:7821–7826.

Gittleman JL (1991) Carnivore olfactory bulb size: Allometry, phylogeny and ecology. J Zool (Lond) 225:253–272.

Gladstone W (1987) The eggs and larvae of the sharpnose pufferfish Canthigaster valentini (Pisces: Tetraodontidae) are unpalatable to other reef fishes. Copeia (1):227–230.

Glaessner MF (1962) Pre-Cambrian fossils. Biol Rev 37:467–494.

Glaessner MF (1984) The Dawn of Animal Life (Cambridge Univ Press, Cambridge, UK).

Glaessner MF, Wade M (1966) The late Precambrian fossils from Ediacara, South Australia. Palaeontology 9:599–628.

Glaessner MF, Wade M (1971) Praecambridium—a primitive arthropod. Lethaia 4:71–77.

Glenner H, Hansen AJ, Sørensen MV, Ronquist F, Huelsenbeck JP, Willerslev E. (2004) Baye-sian inference of the metazoan phylogeny: A combined molecular and morphological approach. Curr Biol 14:1644–1649.

Goaillard JM, Taylor AL, Schulz DJ, Marder E (2009) Functional consequences of animal-to-animal variation in circuit parameters. Nat Neurosci 12:1424–1430.

Göbbeler K, Klussmann-Kolb A (2010) Out of Antarctica—New insights into the phylogeny and biogeography of the Pleurobranchomorpha (Mollusca, Gastropoda). Mol Phylogenet Evol 55:996–1007.

Gohar HAF, Soliman GN (1963) The biology and development of Hexabranchus sanguineus (Ruppell & Leuckart) (Gastropoda, Nudibranchiata). Publ Mar Biol Sta Al-Ghardaqa, Egypt 12:219–247.

Gómez S, Jensen P, Arenas A (2009) Analysis of community structure in networks of correlated data. Phys Rev E Stat Nonlin Soft Matter Phys 80:016114.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Goodman CS, Doe CQ (1993) Embryonic development of the Drosophila CNS. In The Development of Drosophila melanogaster, ed Bate M (Cold Spring Harbor Lab Press, Plainview, NY), pp 1131–1206.

Goodman M, Sterner KN (2010) Phylogenomic evidence of adaptive evolution in the ancestry of humans. Proc Natl Acad Sci USA 107(Suppl 2):8918–8923.

Goodson JL (1998a) Territorial aggression and dawn song are modulated by septal vasotocin and vasoactive intestinal polypeptide in male field sparrows (Spizella pusilla). Horm Behav 34:67–77.

Zeiss atlas 995 topographer

Goodson JL (1998b) Vasotocin and vasoactive intestinal polypeptide modulate aggression in a territorial songbird, the violet-eared waxbill (Estrildidae: Uraeginthus granatina). Gen Comp Endocrinol 111:233–244.

Goodson JL, Bass AH (2001) Social behavior functions and related anatomical characteristics of vasotocin/vasopressin systems in vertebrates. Brain Res Brain Res Rev 35: 246–265.

Goodson JL, Bass AH (2002) Vocal-acoustic circuitry and descending vocal pathways in teleost fish: Convergence with terrestrial vertebrates reveals conserved traits. J Comp Neurol 448:298–322.

Goodson JL, Evans AK (2004) Neural responses to territorial challenge and nonsocial stress in male song sparrows: Segregation, integration, and modulation by a vasopressin V1 antagonist. Horm Behav 46:371–381.

Goodson JL, Kingsbury MA (2011) Nonapeptides and the evolution of social group sizes in birds. Front Neuroanat 5:13.

Goodson JL, Wang Y (2006) Valence-sensitive neurons exhibit divergent functional profiles in gregarious and asocial species. Proc Natl Acad Sci USA 103:17013–17017.

Goodson JL, Evans AK, Lindberg L (2004) Chemoarchitectonic subdivisions of the songbird septum and a comparative overview of septum chemical anatomy in jawed vertebrates. J Comp Neurol 473:293–314.

Goodson JL, Evans AK, Soma KK (2005) Neural responses to aggressive challenge correlate with behavior in nonbreeding sparrows. Neuroreport 16:1719–1723.

Goodson JL, Evans AK, Wang Y (2006) Neuropeptide binding reflects convergent and divergent evolution in species-typical group sizes. Horm Behav 50:223–236.

Goodson JL, Kabelik D, Kelly AM, Rinaldi J, Klatt JD (2009a) Midbrain dopamine neurons reflect affiliation phenotypes in finches and are tightly coupled to courtship. Proc Natl Acad Sci USA 106:8737–8742.

Goodson JL, Schrock SE, Klatt JD, Kabelik D, Kingsbury MA (2009b) Mesotocin and nonapeptide receptors promote estrildid flocking behavior. Science 325:862–866.

Goodson JL, Kelly AK, Kingsbury MA, Thompson RR (2012a). An aggression-specific cell type in the hypothalamus of finches. Proc Natl Acad Sci USA 109:13847–13852.

Goodson JL, Wilson LC, Schrock SE (2012b) To flock or fight: Neurochemical signatures of divergent life histories in sparrows. Proc Natl Acad Sci USA 109(Suppl 1):10685–10692.

Gopnik M (1990) Feature-blind grammar and dysphagia. Nature 344:715.

Gosliner T (1987a) Nudibranchs of Southern Africa: A Guide to Opisthobranch Molluscs of Southern Africa (Sea Challengers, Monterey and El Cajon, CA).

Gosliner TM (1987b) Review of the nudibranch genus Melibe (Opisthobranchia: Dendronotacea) with descriptions of two new species. Veliger 29:400–414.

Gould HJ, 3rd (1986) Body surface maps in the somatosensory cortex of rabbit. J Comp Neurol 243:207–233.

Gould HJ, 3rd, Cusick CG, Pons TP, Kaas JH (1986) The relationship of corpus callosum connections to electrical stimulation maps of motor, supplementary motor, and the frontal eye fields in owl monkeys. J Comp Neurol 247:297–325.

Gould SJ (1977) Ontogeny and Phylogeny (Belknap, Cambridge, MA).

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Grande L, Bemis WE (1998) A Comprehensive Phylogenetic Study of Amiid Fishes (Amiidae) Based on Comparative Skeletal Anatomy. An Empirical Search for Interconnected Patterns of Natural History (Society of Vertebrate Paleontology, Chicago), Memoir, Vol. 4.

Graveley BR, Brooks AN, Carlson JW, Duff MO, Landolin JM, Yang L, Artieri CG, van Baren MJ, Boley N, Booth BW, Brown JB, Cherbas L, Davis CA, Dobin A, Li R, Lin W, Malone JH, Mattiuzzo NR, Miller D, Sturgill D, Tuch BB, Zaleski C, Zhang D, Blanchette M, Dudoit S, Eads B, Green RE, Hammonds A, Jiang L, Kapranov P, Langton L, Perrimon N, Sandler JE, Wan KH, Willingham A, Zhang Y, Zou Y, Andrews J, Bickel PJ, Brenner SE, Brent MR, Cherbas P, Gingeras TR, Hoskins RA, Kaufman TC, Oliver B, Celniker SE (2011) The developmental transcriptome of Drosophila melanogaster. Nature 471:473–479.

Graziano MSA, Taylor CSR, Moore T (2002) Complex movements evoked by microstimulation of precentral cortex. Neuron 34:841–851.

Greenfield DW, Winterbottom R, Collette BB (2008) Review of the toadfish genera (Teleostei: Batrachoididae). Proc Calif Acad Sci 59:665–710.

Greenlaw JS (1996) Eastern towhee (Pipilo erythropthalmus). Birds North Am 262:1–32.

Grinstein G, Linsker R (2005) Synchronous neural activity in scale-free network models versus random network models. Proc Natl Acad Sci USA 102:9948–9953.

Gross CG (1998) Brain, vision, memory: Tales in the History of Neuroscience (MIT Press, Cambridge, MA).

Grossman LI, Schmidt TR, Wildman DE, Goodman M (2001) Molecular evolution of aerobic energy metabolism in primates. Mol Phylogenet Evol 18:26–36.

Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE (2008) Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr Biol 18:354–362.

Grubb MS, Burrone J (2010) Activity-dependent relocation of the axon initial segment fine-tunes neuronal excitability. Nature 465:1070–1074.

Günther A (1870) Description of Ceratodus, a genus of ganoid fishes, recently discovered in rivers of Queensland, Australia. Proc R Soc Lond 19:377–379.

Hackett TA, Stepniewska I, Kaas JH (1998) Thalamocortical connections of the parabelt auditory cortex in macaque monkeys. J Comp Neurol 400:271–286.

Hackett TA, Stepniewska I, Kaas JH (1999) Prefrontal connections of the parabelt auditory cortex in macaque monkeys. Brain Res 817:45–58.

Haefelfinger HR, Kress A (1967) Der Schwimmvorgang bei Gasteropteron rubrum (Rafinesque 1814) (Gastropoda, Opisthobranchiata). Rev Suisse Zool 74:547–554.

Haesler S, Wada K, Nshdejan A, Morrisey EE, Lints T, Jarvis ED, Scharff C (2004) FoxP2 expression in avian vocal learners and non-learners. J Neurosci 24:3164–3175.

Haesler S, Rochefort C, Georgi B, Licznerski P, Osten P, Scharff C (2007) Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus area X. PLoS Biol 5:e321.

Hagena H, Manahan-Vaughan D (2011) Learning-facilitated synaptic plasticity at CA3 mossy fiber and commissural-associational synapses reveals different roles in information processing. Cereb Cortex 21:2442–2449.

Halanych KM, Passamaneck Y (2001) A brief review of metazoan phylogeny and future prospects in Hox-research. Am Zool 41:629–639.

Halberda J, Mazzocco MM, Feigenson L (2008) Individual differences in non-verbal number acuity correlate with maths achievement. Nature 455:665–668.

Halfter W, Dong S, Yip YP, Willem M, Mayer U (2002) A critical function of the pial basement membrane in cortical histogenesis. J Neurosci 22:6029–6040.

Hall BK (1995) Homology and embryonic development. Evol Biol 28:1–36.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Hamasaki T, Leingärtner A, Ringstedt T, O’Leary DD (2004) EMX2 regulates sizes and positioning of the primary sensory and motor areas in neocortex by direct specification of cortical progenitors. Neuron 43:359–372.

Hamilton WJ (1931) Habits of the star-nosed mole, Condylura cristata. J Mammal 12:345–355.

Hanneman E, Trevarrow B, Metcalfe WK, Kimmel CB, Westerfield M (1988) Segmental pattern of development of the hindbrain and spinal cord of the zebrafish embryo. Development 103:49–58.

Hansen DV, Rubenstein JLR, Kriegstein AR (2011) Deriving excitatory neurons of the neocortex from pluripotent stem cells. Neuron 70:645–660.

Hara E, Rivas MV, Ward JM, Okanoya K, Jarvis ED (2012) Convergent differential regulation of parvalbumin in the brains of vocal learners. PLoS ONE 7:e29457.

Harshman J, Braun EL, Braun MJ, Huddleston CJ, Bowie RC, Chojnowski JL, Hackett SJ, Han KL, Kimball RT, Marks BD, Miglia KJ, Moore WS, Reddy S, Sheldon FH, Steadman DW, Steppan SJ, Witt CC, Yuri T (2008) Phylogenomic evidence for multiple losses of flight in ratite birds. Proc Natl Acad Sci USA 105:13462–13467.

Hartline DK, Colman DR (2007) Rapid conduction and the evolution of giant axons and myelinated fibers. Curr Biol 17:R29–R35.

Hasenstaub A, Otte S, Callaway E, Sejnowski TJ (2010) Metabolic cost as a unifying principle governing neuronal biophysics. Proc Natl Acad Sci USA 107:12329–12334.

Haug H (1987) Brain sizes, surfaces, and neuronal sizes of the cortex cerebri: A stereological investigation of man and his variability and a comparison with some mammals (primates, whales, marsupials, insectivores, and one elephant). Am J Anat 180(2):126–142.

Hays GC, Akesson S, Broderick AC, Glen F, Godley BJ, Papi F, Luschi P (2003) Island-finding ability of marine turtles. Proc Biol Sci 270(Suppl 1):S5–S7.

Healy S, Guilford T (1990) Olfactory-bulb size and nocturnality in birds. Evolution 44:339–346.

Heideman PD (2004) Top-down approaches to the study of natural variation in complex physiological pathways using the white-footed mouse (Peromyscus leucopus) as a model. ILAR J 45:4–13.

Heil P, Bronchti G, Wollberg Z, Scheich H (1991) Invasion of visual cortex by the auditory system in the naturally blind mole rat. Neuroreport 2:735–738.

Heiligenberg W (1991) Sensory control of behavior in electric fish. Curr Opin Neurobiol 1:633–637.

Heiman M, Schaefer A, Gong S, Peterson JD, Day M, Ramsey KE, Suárez-Fariñas M, Schwarz C, Stephan DA, Surmeier DJ, Greengard P, Heintz N (2008) A translational profiling approach for the molecular characterization of CNS cell types. Cell 135:738–748.

Hein G, Doehrmann O, Müller NG, Kaiser J, Muckli L, Naumer MJ (2007) Object familiarity and semantic congruency modulate responses in cortical audiovisual integration areas. J Neurosci 27:7881–7887.

Heinroth O (1911) Beiträge zur Biologie, namentlich Ethologie und Psychologie der Anatiden. Verh Int Ornithol Kongr Berlin 5:589-702.

Hejnol A, Obst M, Stamatakis A, Ott M, Rouse GW, Edgecombe GD, Martinez P, Baguñà J, Bailly X, Jondelius U, Wiens M, Müller WE, Seaver E, Wheeler WC, Martindale MQ, Giribet G, Dunn CW (2009) Assessing the root of bilaterian animals with scalable phylogenomic methods. Proc Biol Sci 276:4261–4270.

Helmuth L (2001) Neuroscience. Glia tell neurons to build synapses. Science 291:569–570.

Hendrickson AE (1985) Dots, stripes and columns in monkey visual cortex. Trends Neurosci 8:406–410.

Hennig W (1966) Phylogenetic Systematics (Univ of Illinois Press, Urbana).

Henrich J, McElreath R (2003) The evolution of cultural evolution. Evol Anthropol 12:123–135.

Hepper PG, Wells DL (2005) How many footsteps do dogs need to determine the direction of an odour trail? Chem Senses 30:291–298.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Herculano-Houzel S (2009) The human brain in numbers: A linearly scaled-up primate brain. Front Hum Neurosci 3:31.

Herculano-Houzel S (2010) Coordinated scaling of cortical and cerebellar numbers of neurons. Front Neuroanat 4:12.

Herculano-Houzel S (2011a) Brains matter, bodies maybe not: The case for examining neuron numbers irrespective of body size. Ann N Y Acad Sci 1225:191–199.

Herculano-Houzel S (2011b) Not all brains are made the same: New views on brain scaling in evolution. Brain Behav Evol 78:22–36.

Herculano-Houzel S (2011c) Scaling of brain metabolism with a fixed energy budget per neuron: Implications for neuronal activity, plasticity and evolution. PLoS ONE 6:e17514.

Herculano-Houzel S (2012) Neuronal scaling rules for primate brains: The primate advantage. Prog Brain Res 195:325–340.

Herculano-Houzel S, Kaas JH (2011) Great ape brains conform to the primate scaling rules: Implications for hominin evolution. Brain Behav Evol 77:33–44.

Herculano-Houzel S, Lent R (2005) Isotropic fractionator: A simple, rapid method for the quantification of total cell and neuron numbers in the brain. J Neurosci 25:2518–2521.

Herculano-Houzel S, Mota B, Lent R (2006) Cellular scaling rules for rodent brains. Proc Natl Acad Sci USA 103:12138–12143.

Herculano-Houzel S, Collins CE, Wong P, Kaas JH (2007) Cellular scaling rules for primate brains. Proc Natl Acad Sci USA 104:3562–3567.

Herculano-Houzel S, Collins CE, Wong P, Kaas JH, Lent R (2008) The basic nonuniformity of the cerebral cortex. Proc Natl Acad Sci USA 105:12593–12598.

Herculano-Houzel S, Mota B, Wong P, Kaas JH (2010) Connectivity-driven white matter scaling and folding in primate cerebral cortex. Proc Natl Acad Sci USA 107:19008–19013.

Herculano-Houzel S, Ribeiro P, Campos L, Valotta da Silva A, Torres LB, Catania KC, Kaas JH (2011) Updated neuronal scaling rules for the brains of Glires (rodents/lagomorphs). Brain Behav Evol 78:302–314.

Herrmann E, Call J, Hernàndez-Lloreda MV, Hare B, Tomasello M (2007) Humans have evolved specialized skills of social cognition: The cultural intelligence hypothesis. Science 317:1360–1366.

Hickok G, Poeppel D (2007) The cortical organization of speech processing. Nat Rev Neurosci 8:393–402.

Higashijima S, Hotta Y, Okamoto H (2000) Visualization of cranial motor neurons in live transgenic zebrafish expressing green fluorescent protein under the control of the islet-1 promoter/enhancer. J Neurosci 20:206–218.

Hill AS, Nishino A, Nakajo K, Zhang G, Fineman JR, Selzer ME, Okamura Y, Cooper EC (2008) Ion channel clustering at the axon initial segment and node of Ranvier evolved sequentially in early chordates. PLoS Genet 4:e1000317.

Hille B (2001) Ion Channels of Excitable Membranes (Sinauer Press, Sunderland, MA).

Hillier LW, Reinke V, Green P, Hirst M, Marra MA, Waterston RH (2009) Massively parallel sequencing of the polyadenylated transcriptome of C. elegans. Genome Res 19:657–666.

Hingee M, Magrath RD (2009) Flights of fear: A mechanical wing whistle sounds the alarm in a flocking bird. Proc R Soc B 276:4173–4179.

Hirth F (2010) On the origin and evolution of the tripartite brain. Brain Behav Evol 76:3–10.

Hirth F, Reichert H (2007) Basic nervous system types: One or many? In The Evolution of Nervous Systems, eds Streidter G, Rubenstein JL (Academic Press, Oxford), Vol 1, pp 55–72.

Hirth F, Kammermeier L, Frei E, Walldorf U, Noll M, Reichert H (2003) An urbilaterian origin of the tripartite brain: Developmental genetic insights from Drosophila. Development 130:2365–2373.

Hodgkin AL, Huxley AF (1952) A quantitative description of membrane current and its application to conduction and excitation in nerve. J Physiol 117:500–544.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Hoekstra HE, Price T (2004) Evolution. Parallel evolution is in the genes. Science 303: 1779–1781.

Hofman MA (1985) Size and shape of the cerebral cortex in mammals. I. The cortical surface. Brain Behav Evol 27:28–40.

Hofman MA (1988) Size and shape of the cerebral cortex in mammals. II. The cortical volume. Brain Behav Evol 32:17–26.

Holding ML, Frazier JA, Taylor EN, Strand CR (2012) Experimentally altered navigational demands induce changes in the cortical forebrain of free-ranging northern Pacific rattlesnakes (Crotalus o. oreganus). Brain Behav Evol 79:144–154.

Holland PWH, Takahashi T (2005) The evolution of homeobox genes: Implications for the study of brain development. Brain Res Bull 66:484–490.

Holland RA, Thorup K, Gagliardo A, Bisson IA, Knecht E, Mizrahi D, Wikelski M (2009) Testing the role of sensory systems in the migratory heading of a songbird. J Exp Biol 212:4065–4071.

Holley SA, Jackson PD, Sasai Y, Lu B, De Robertis EM, Hoffmann FM, Ferguson EL (1995) A conserved system for dorsal-ventral patterning in insects and vertebrates involving sog and chordin. Nature 376:249–253.

Holloway ID, Ansari D (2008) Domain-specific and domain-general changes in children’s development of number comparison. Dev Sci 11:644–649.

Holloway ID, Ansari D (2009) Mapping numerical magnitudes onto symbols: The numerical distance effect and individual differences in children’s mathematics achievement. J Exp Child Psychol 103:17–29.

Holloway ID, Ansari D (2010) Developmental specialization in the right intraparietal sulcus for the abstract representation of numerical magnitude. J Cogn Neurosci 22:2627–2637.

Holstege G (1989) Anatomical study of the final common pathway for vocalization in the cat. J Comp Neurol 284:242–252.

Holyoak KJ (1977) Form of analog size information in memory. Cognit Psychol 9:31–51.

Homae F, Hashimoto R, Nakajima K, Miyashita Y, Sakai KL (2002) From perception to sentence comprehension: The convergence of auditory and visual information of language in the left inferior frontal cortex. Neuroimage 16:883–900.

Horton JC (1984) Cytochrome oxidase patches: A new cytoarchitectonic feature of monkey visual cortex. Philos Trans R Soc Lond B Biol Sci 304:199–253.

Horton JC, Adams DL (2005) The cortical column: A structure without a function. Philos Trans R Soc Lond B Biol Sci 360:837–862.

Horton JC, Hedley-Whyte ET (1984) Mapping of cytochrome oxidase patches and ocular dominance columns in human visual cortex. Philos Trans R Soc Lond B Biol Sci 304: 255–272.

Hu W, Tian C, Li T, Yang M, Hou H, Shu Y (2009) Distinct contributions of Na(v)1.6 and Na(v)1.2 in action potential initiation and backpropagation. Nat Neurosci 12:996–1002.

Hua JY, Smith SJ (2004) Neural activity and the dynamics of central nervous system development. Nat Neurosci 7:327–332.

Huang R, Zhi Q, Izpisua-Belmonte JC, Christ B, Patel K (1999) Origin and development of the avian tongue muscles. Anat Embryol (Berl) 200:137–152.

Hubel DH, Livingstone MS (1987) Segregation of form, color, and stereopsis in primate area 18. J Neurosci 7:3378–3415.

Hubel DH, Wiesel TN (1963) Shape and arrangement of columns in cat’s striate cortex. J Physiol 165:559–568.

Hubel DH, Wiesel TN (1968) Receptive fields and functional architecture of monkey striate cortex. J Physiol 195:215–243.

Hubel DH, Wiesel TN (1972) Laminar and columnar distribution of geniculo-cortical fibers in the macaque monkey. J Comp Neurol 146:421–450.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Hubel DH, Wiesel TN (1977) Ferrier lecture: Functional architecture of macaque monkey visual cortex. Proc R Soc Lond B Biol Sci 198:1–59.

Hughes AL (1994) The evolution of functionally novel proteins after gene duplication. Proc Biol Sci 256:119–124.

Hughes CL, Kaufman TC (2002) Hox genes and the evolution of the arthropod body plan. Evol Dev 4:459–499.

Hulbert AJ, Else PL (1989) Evolution of mammalian endothermic metabolism: Mitochondrial activity and cell composition. Am J Physiol 256(Pt 2):R63–R69.

Huldtgren T, Cunningham JA, Yin C, Stampanoni M, Marone F, Donoghue PC, Bengtson S (2011) Fossilized nuclei and germination structures identify Ediacaran “animal embryos” as encysting protists. Science 334:1696–1699.

Hume RI, Getting PA, Del Beccaro MA (1982) Motor organization of Tritonia swimming. I. Quantitative analysis of swim behavior and flexion neuron firing patterns. J Neurophysiol 47:60–74.

Hunt DL, King B, Kahn DM, Yamoah EN, Shull GE, Krubitzer L (2005) Aberrant retinal projections in congenitally deaf mice: How are phenotypic characteristics specified in development and evolution? Anat Rec A Discov Mol Cell Evol Biol 287:1051–1066.

Hurst A (1968) The feeding mechanism and behavior of the opisthobranch Melibe leonina. Symp Zool Soc Lond 22:155–166.

Hurst JA, Baraitser M, Auger E, Graham F, Norell S (1990) An extended family with a dominantly inherited speech disorder. Dev Med Child Neurol 32:352–355.

Huxley T (1863a) Evidence as to Man’s Place in Nature (Williams and Norgate, London).

Huxley TH (1863b) Man’s Place in Nature (Univ Michigan Press, Ann Arbor).

Iggo A, Gregory JE, Proske U (1996) Studies of mechanoreceptors in skin of the snout of the echidna Tachyglossus aculeatus. Somatosens Mot Res 13:129–138.

Itakura T, Chandra A, Yang Z, Xue X, Wang B, Kimura W, Hikosaka K, Inohaya K, Kudo A, Uezato T, Miura N (2008) The medaka FoxP2, a homologue of human language gene FOXP2, has a diverged structure and function. J Biochem 143:407–416.

Iverson JM, Fagan MK (2004) Infant vocal-motor coordination: Precursor to the gesture-speech system? Child Dev 75:1053–1066.

Iverson JM, Thelen E (1999) Hand, mouth and brain. The dynamic emergence of speech and gesture. J Conscious Stud 6:19–40.

Iwaniuk AN, Hurd PL (2005) The evolution of cerebrotypes in birds. Brain Behav Evol 65: 215–230.

Jackendoff R (1999) Possible stages in the evolution of the language capacity. Trends Cogn Sci 3:272–279.

Jacob F (1977) Evolution and tinkering. Science 196:1161–1166.

Jacobs LF (2003) The evolution of the cognitive map. Brain Behav Evol 62:128–139.

Jacobs LF (2006) From movement to transitivity: The role of hippocampal parallel maps in configural learning. Rev Neurosci 17:99–109.

Jacobs LF (2009) The role of social selection in the evolution of hippocampal specialization. In Cognitive Biology: Evolutionary and Developmental Perspectives on Mind, Brain and Behavior, eds Tomassi L, Nadel L, Peterson M (MIT Press, Cambridge, MA).

Jacobs LF (2012) From chemotaxis to the cognitive map: The function of olfaction. Proc Natl Acad Sci USA 109(Suppl 1):10693–10700.

Jacobs LF, Schenk F (2003) Unpacking the cognitive map: The parallel map theory of hippocampal function. Psychol Rev 110:285–315.

Jacobs R (1997) Nature, nurture, and the development of functional specializations: A computational approach. Psychon Bull Rev 4:299–309.

Jaillon O, Aury JM, Brunet F, Petit JL, Stange-Thomann N, Mauceli E, Bouneau L, Fischer C, Ozouf-Costaz C, Bernot A, Nicaud S, Jaffe D, Fisher S, Lutfalla G, Dossat C, Segurens B, Dasilva C, Salanoubat M, Levy M, Boudet N, Castellano S, Anthouard V, Jubin

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

C, Castelli V, Katinka M, Vacherie B, Biémont C, Skalli Z, Cattolico L, Poulain J, De Berardinis V, Cruaud C, Duprat S, Brottier P, Coutanceau JP, Gouzy J, Parra G, Lardier G, Chapple C, McKernan KJ, McEwan P, Bosak S, Kellis M, Volff JN, Guigó R, Zody MC, Mesirov J, Lindblad-Toh K, Birren B, Nusbaum C, Kahn D, Robinson-Rechavi M, Laudet V, Schachter V, Quétier F, Saurin W, Scarpelli C, Wincker P, Lander ES, Weissenbach J, Roest Crollius H (2004) Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype. Nature 431:946–957.

Jain N, Catania KC, Kaas JH (1998) A histologically visible representation of the fingers and palm in primate area 3b and its immutability following long-term deafferentations. Cereb Cortex 8:227–236.

Jain N, Qi HX, Catania KC, Kaas JH (2001) Anatomic correlates of the face and oral cavity representations in the somatosensory cortical area 3b of monkeys. J Comp Neurol 429:455–468.

Janvier P (2003) Vertebrate characters and the Cambrian vertebrates. C R Palevol 2:523–531.

Janvier P (2008) Early jawless vertebrates and cyclostome origins. Zoolog Sci 25:1045–1056.

Jenner RA (2004) When molecules and morphology clash: Reconciling conflicting phylogenies of the Metazoa by considering secondary character loss. Evol Dev 6:372–378.

Jensen S, Droser ML, Gehling JG (2006) A critical look at the Ediacaran trace fossil record. In Neoproterozoic Geobiology and Paleobiology, eds Xiao S, Kaufman AJ (Springer, Berlin), pp 115–157.

Jerison HJ (1973) Evolution of the Brain and Intelligence (Academic Press, New York).

Jerison HJ (1977) The theory of encephalization. Ann N Y Acad Sci 299:146–160.

Jerison HJ (1985) Animal intelligence as encephalization. Philos Trans R Soc Lond B Biol Sci 308(1135):21–35.

Jerison HJ (2007) How can fossils tell us about the evolution of the neocortex? In Evolution of Nervous Systems: A Comprehensive Reference, ed Kaas J (Elsevier, Oxford), Vol 3, pp 500–508.

Jing J, Gillette R (1995) Neuronal elements that mediate escape swimming and suppress feeding behavior in the predatory sea slug Pleurobranchaea. J Neurophysiol 74:1900–1910.

Jing J, Gillette R (1999) Central pattern generator for escape swimming in the notaspid sea slug Pleurobranchaea californica. J Neurophysiol 81:654–667.

Jing J, Gillette R (2000) Escape swim network interneurons have diverse roles in behavioral switching and putative arousal in Pleurobranchaea. J Neurophysiol 83:1346–1355.

Jing J, Vilim FS, Cropper EC, Weiss KR (2008) Neural analog of arousal: Persistent conditional activation of a feeding modulator by serotonergic initiators of locomotion. J Neurosci 28:12349–12361.

Johnson MB, Kawasawa YI, Mason CE, Krsnik Z, Coppola G, Bogdanovi´c D, Geschwind DH, Mane SM, State MW, Sestan N (2009) Functional and evolutionary insights into human brain development through global transcriptome analysis. Neuron 62:494–509.

Johnson MH, Dziurawiec S, Ellis H, Morton J (1991) Newborns’ preferential tracking of face-like stimuli and its subsequent decline. Cognition 40:1–19.

Johnson S (1984) A new Indo-West Pacific species of the dendronotacean nudibranch Bornella (Mollusca: Opisthobranchia) with anguilliform swimming behaviour. Micronesica 19:17–26.

Johnson-Frey SH (2004) The neural bases of complex tool use in humans. Trends Cogn Sci 8:71–78.

Johnston CE, Phillips CT (2003) Sound production in sturgeon Scaphirhynchus albust and S. platorynchus (Acipenseridae). Environ Biol Fishes 68:59–64.

Jones CM, Liyanapathirana M, Agossa FR, Weetman D, Ranson H, Donnelly MJ, Wilding CS (2012) Footprints of positive selection associated with a mutation (N1575Y) in the voltage-gated sodium channel of Anopheles gambiae. Proc Natl Acad Sci USA 109:6614–6619.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Jones EG, Powell TP (1970) An anatomical study of converging sensory pathways within the cerebral cortex of the monkey. Brain 93:793–820.

Jones EG, Dell’Anna ME, Molinari M, Rausell E, Hashikawa T (1995) Subdivisions of macaque monkey auditory cortex revealed by calcium-binding protein immunore-activity. J Comp Neurol 362:153–170.

Jones JA, Callan DE (2003) Brain activity during audiovisual speech perception: An fMRI study of the McGurk effect. Neuroreport 14:1129–1133.

Jordan KE, Brannon EM, Logothetis NK, Ghazanfar AA (2005) Monkeys match the number of voices they hear to the number of faces they see. Curr Biol 15:1034–1038.

Jost MC, Hillis DM, Lu Y, Kyle JW, Fozzard HA, Zakon HH (2008) Toxin-resistant sodium channels: Parallel adaptive evolution across a complete gene family. Mol Biol Evol 25:1016–1024.

Jürgens U (2009) The neural control of vocalization in mammals: A review. J Voice 23:1–10.

Jürgens U, Hage SR (2007) On the role of the reticular formation in vocal pattern generation. Behav Brain Res 182:308–314.

Kaas JH (1984) Duplication of brain parts in evolution. Behav Brain Sci 7:342–343.

Kaas JH (1989) The evolution of complex sensory systems in mammals. J Exp Biol 146:165–176.

Kaas JH (2000) Why is brain size so important: Design problems and solutions as neocortex gets bigger or smaller. Brain Mind 1:7–23.

Kaas JH (2003) The evolution of the visual system in primates. In The Visual Neurosciences, eds Chalupa LM, Werner JS (MIT Press, Cambridge, MA), pp 1563–1572.

Kaas JH (2007) Reconstructing the organization of the neocortex of the first mammals and subsequent modifications. In Evolution of Nervous Systems, eds Kaas JH, Krubitzer LA (Elsevier, London), pp 27–48.

Kaas JH (2010) Cortical circuits: Consistency and variability across cortical areas and species. In Dynamic Coordination in the Brain: From Neurons to Mind. 2010 Strügmann Forum Report, eds Philips WA, Singer W (MIT Press, Cambridge, MA), pp 25–34.

Kaas JH (2011) The evolution of auditory cortex: The core areas. In The Auditory Cortex, eds Winer JA, Schreiner CE (Springer-Verlag, New York), pp 407–427.

Kaas JH, Catania KC (2002) How do features of sensory representations develop? Bioessays 24:334–343.

Kaas JH, Morel A (1993) Connections of visual areas of the upper temporal lobe of owl monkeys: The MT crescent and dorsal and ventral subdivisions of FST. J Neurosci 13:534–546.

Kaas JH, Preuss TM (2008) Human brain evolution. In Fundamental Neuroscience, ed Squire LR (Academic Press, San Diego), pp 1027–1035.

Kaas JH, Guillery RW, Allman JM (1973) The representation of the optic disc in the dorsal lateral geniculate nucleus: A comparative study. J Comp Neurol 147:163–180.

Kaas JH, Gharbawie OA, Stepniewska I (2011) The organization and evolution of dorsal stream multisensory motor pathways in primates. Front Neuroanat 5:1–7.

Kabelik D, Kelly AM, Goodson JL (2010) Dopaminergic regulation of mate competition aggression and aromatase-Fos colocalization in vasotocin neurons. Neuropharmacology 58:117–125.

Kadner D, Stollewerk A (2004) Neurogenesis in the chilopod Lithobius forficatus suggests more similarities to chelicerates than to insects. Dev Genes Evol 214:367–379.

Kahn DM, Krubitzer L (2002) Massive cross-modal cortical plasticity and the emergence of a new cortical area in developmentally blind mammals. Proc Natl Acad Sci USA 99: 11429–11434.

Kandel E, Schwartz J, Jessel T (2004) Principles of Neural Science (McGraw-Hill, New York), 4th Ed, p 20.

Kaneko Y, Matsumoto G, Hanyu Y (1997) TTX resistivity of Na+ channel in newt retinal neuron. Biochem Biophys Res Commun 240:651–656.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Kang W, Wong LC, Shi SH, Hébert JM (2009) The transition from radial glial to intermediate progenitor cell is inhibited by FGF signaling during corticogenesis. J Neurosci 29:14571–14580.

Kania A, Jessell TM (2003) Topographic motor projections in the limb imposed by LIM homeodomain protein regulation of ephrin-A:EphA interactions. Neuron 38:581–596.

Kannan R, Berger C, Myneni S, Technau GM, Shashidhara LS (2010) Abdominal-A mediated repression of cyclin E expression during cell-fate specification in the Drosophila central nervous system. Mech Dev 127:137–145.

Kanwisher N, Yovel G (2006) The fusiform face area: A cortical region specialized for the perception of faces. Philos Trans R Soc Lond B Biol Sci 361:2109–2128.

Kaplan HS, Hill K, Lancaster JL, Hurtado AM (2000) A theory of human life history evolution: Diet, intelligence, and longevity. Ev Anth 9:156–185.

Kappelman J (1996) The evolution of body mass and relative brain size in fossil hominids. J Hum Evol 30:243–276.

Karbowski J (2001) Optimal wiring principle and plateaus in the degree of separation for cortical neurons. Phys Rev Lett 86:3674–3677.

Karbowski J (2003) How does connectivity between cortical areas depend on brain size? Implications for efficient computation. J Comput Neurosci 15:347–356.

Karbowski J (2007) Global and regional brain metabolic scaling and its functional consequences. BMC Biol 5:18.

Karlen SJ, Krubitzer L (2006) Phenotypic diversity is the cornerstone of evolution: Variation in cortical field size within short-tailed opossums. J Comp Neurol 499:990–999.

Karlen SJ, Krubitzer L (2007) The functional and anatomical organization of marsupial neocortex: Evidence for parallel evolution across mammals. Prog Neurobiol 82:122–141.

Karlen SJ, Kahn DM, Krubitzer L (2006) Early blindness results in abnormal corticocortical and thalamocortical connections. Neuroscience 142:843–858.

Karmiloff-Smith A (1992) Beyond Modularity: A Developmental Perspective on Cognitive Science (MIT Press, Cambridge, MA).

Kaschube M, Schnabel M, Löwel S, Coppola DM, White LE, Wolf F (2010) Universality in the evolution of orientation columns in the visual cortex. Science 330:1113–1116.

Kaskan PM, Lu HD, Dillenburger BC, Roe AW, Kaas JH (2007) Intrinsic-signal optical imaging reveals cryptic ocular dominance columns in primary visual cortex of New World owl monkeys. Front Neurosci 1:67–75.

Kaskan PM, Lu HD, Dillenburger BC, Kaas JH, Roe AW (2009) The organization of orientation-selective, luminance-change and binocular-preference domains in the second (V2) and third (V3) visual areas of New World owl monkeys as revealed by intrinsic signal optical imaging. Cereb Cortex 19:1394–1407.

Kaskan PM, Dillenburger BC, Lu HD, Roe AW, Kaas JH (2010) Orientation and direction-of-motion response in the middle temporal visual area (MT) of New World owl monkeys as revealed by intrinsic-signal optical imaging. Front Neuroanat 4:1–12.

Kastberger G (1981) Economy of sound production in piranhas (Serrasalminae, Characidae): II. Functional properties of sound emitter. Zool Jb Physiol 85:393–411.

Katz LC, Constantine-Paton M (1988) Relationships between segregated afferents and postsynaptic neurones in the optic tectum of three-eyed frogs. J Neurosci 8:3160–3180.

Katz PS (2009) Tritonia swim network. Scholarpedia 4:3638.

Katz PS (2010) The Tritonia swim central pattern generator. In Handbook of Brain Microcircuits, eds Shepherd G, Grillner S (Oxford Univ Press, New York), pp 443–449.

Katz PS (2011) Neural mechanisms underlying the evolvability of behaviour. Philos Trans R Soc Lond B Biol Sci 366:2086–2099.

Katz PS, Getting PA, Frost WN (1994) Dynamic neuromodulation of synaptic strength intrinsic to a central pattern generator circuit. Nature 367:729–731.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Kawasaki M (2009) Evolution of time-coding systems in weakly electric fishes. Zoolog Sci 26:587–599.

Kay LM, Beshel J, Brea J, Martin C, Rojas-Líbano D, Kopell N (2009) Olfactory oscillations: The what, how and what for. Trends Neurosci 32:207–214.

Kay LM, Crk T, Thorngate J (2005) A redefinition of odor mixture quality. Behav Neurosci 119:726–733.

Kayser C, Logothetis NK, Panzeri S (2010) Visual enhancement of the information representation in auditory cortex. Curr Biol 20:19–24.

Kelly AM, Kingsbury MA, Hoffbuhr K, Schrock SE, Waxman B, Kabelik D, Thompson RR, Goodson JL (2011) Vasotocin neurons and septal V1a-like receptors potently modulate songbird flocking and responses to novelty. Horm Behav 60:12–21.

Kemp A, Manahan-Vaughan D (2008) The hippocampal CA1 region and dentate gyrus differentiate between environmental and spatial feature encoding through long-term depression. Cereb Cortex 18:968–977.

Khaitovich P, Muetzel B, She X, Lachmann M, Hellmann I, Dietzsch J, Steigele S, Do HH, Weiss G, Enard W, Heissig F, Arendt T, Nieselt-Struwe K, Eichler EE, Pääbo S (2004) Regional patterns of gene expression in human and chimpanzee brains. Genome Res 14:1462–1473.

Khaitovich P, Enard W, Lachmann M, Pääbo S (2006) Evolution of primate gene expression. Nat Rev Genet 7:693–702.

Kidokoro Y, Grinnell A, Eaton D (1974) Tetrodotoxin sensitivity of muscle action potentials in pufferfishes and related fishes. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 89:59–72.

Kim JN, Shadlen MN (1999) Neural correlates of a decision in the dorsolateral prefrontal cortex of the macaque. Nat Neurosci 2:176–185.

Kimmel CB, Metcalfe WK, Schabtach E (1985) T reticular interneurons: A class of serially repeating cells in the zebrafish hindbrain. J Comp Neurol 233:365–376.

Kimura M (1968) Evolutionary rate at the molecular level. Nature 217:624–626.

King MC, Wilson AC (1975) Evolution at two levels in humans and chimpanzees. Science 188:107–116.

Kingsbury MA, Rehen SK, Contos JJA, Higgins CM, Chun J (2003) Non-proliferative effects of lysophosphatidic acid enhance cortical growth and folding. Nat Neurosci 6: 1292–1299.

Kingsbury MA, Kelly AM, Schrock SE, Goodson JL (2011) Mammal-like organization of the avian midbrain central gray and a reappraisal of the intercollicular nucleus. PLoS ONE 6:e20720.

Kinkhabwala A, Riley M, Koyama M, Monen J, Satou C, Kimura Y, Higashijima S, Fetcho J (2011) A structural and functional ground plan for neurons in the hindbrain of zebra-fish. Proc Natl Acad Sci USA 108:1164–1169.

Kirkham NZ, Slemmer JA, Johnson SP (2002) Visual statistical learning in infancy: Evidence for a domain general learning mechanism. Cognition 83:B35–B42.

Kirschner M, Gerhart J (1998) Evolvability. Proc Natl Acad Sci USA 95:8420–8427.

Kittelberger JM, Land BR, Bass AH (2006) Midbrain periaqueductal gray and vocal patterning in a teleost fish. J Neurophysiol 96:71–85.

Kjerschow-Agersborg HP (1921) Contributions to the knowledge of the nudibranchiate mollusk, Melibe leonina (Gould). Am Nat 55:222–253.

Kjerschow-Agersborg HP (1922) Notes on the locomotion of the nudibranchiate mollusk Dendronotus giganteous O’Donoghue. Biol Bull 42:257–266.

Kleiber M (1932) Body size and metabolism. Hilgardia 6:315–353.

Kluessendorf J, Doyle P (2000) Pohlsepia mazonensis, an early “octopus” from the Carboniferous of Illinois, USA. Palaeontology 43:919–926.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Koehl MAR (2006) The fluid mechanics of arthropod sniffing in turbulent odor plumes. Chem Senses 31:93–105.

Koishi R, Xu H, Ren D, Navarro B, Spiller BW, Shi Q, Clapham DE (2004) A superfamily of voltage-gated sodium channels in bacteria. J Biol Chem 279:9532–9538.

Kole MHP, Ilschner SU, Kampa BM, Williams SR, Ruben PC, Stuart GJ (2008) Action potential generation requires a high sodium channel density in the axon initial segment. Nat Neurosci 11:178–186.

Kollack-Walker S, Watson SJ, Akil H (1997) Social stress in hamsters: Defeat activates specific neurocircuits within the brain. J Neurosci 17:8842–8855.

Konishi M (2010) From central pattern generator to sensory template in the evolution of birdsong. Brain Lang 115:18–20.

Konopka G, Bomar JM, Winden K, Coppola G, Jonsson ZO, Gao F, Peng S, Preuss TM, Wohlschlegel JA, Geschwind DH (2009a) Human-specific transcriptional regulation of CNS development genes by FOXP2. Nature 462:213–217.

Konopka G, Davis-Turak J, Oldham M, Friedrich T, O’Connor B, Coppola G, Gao F, Nelson SF, Preuss TM, Geschwind DH (2009b) Comparative gene expression in primate brain. Society for Neuroscience Abstracts, Program No. 225.1/B76 (Society for Neuroscience, Washington, DC), pp 1–2.

Koonin EV (2005) Orthologs, paralogs, and evolutionary genomics. Annu Rev Genet 39: 309–338.

Korn H, Faber DS (2005) The Mauthner cell half a century later: A neurobiological model for decision-making? Neuron 47:13–28.

Kosonsiriluk S, Sartsoongnoen N, Chaiyachet OA, Prakobsaeng N, Songserm T, Rozenboim I, Halawani ME, Chaiseha Y (2008) Vasoactive intestinal peptide and its role in continuous and seasonal reproduction in birds. Gen Comp Endocrinol 159:88–97.

Koyama M, Kinkhabwala A, Satou C, Higashijima S, Fetcho J (2011) Mapping a sensory-motor network onto a structural and functional ground plan in the hindbrain. Proc Natl Acad Sci USA 108:1170–1175.

Kratochvil H (1978) Der Bau des Lautapparates vom knurrenden Gurami (Trichopsis vittatus; Cuvier & Valenciennes) (Anabantidae, Belontiidae). Zoomorphology 91:91–99.

Kriegstein A, Alvarez-Buylla A (2009) The glial nature of embryonic and adult neural stem cells. Annu Rev Neurosci 32:149–184.

Kriegstein A, Noctor S, Martínez-Cerdeño V (2006) Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion. Nat Rev Neurosci 7:883–890.

Krubitzer L (2007) The magnificent compromise: Cortical field evolution in mammals. Neuron 56:201–208.

Krubitzer L (2009) In search of a unifying theory of complex brain evolution. Ann N Y Acad Sci 1156:44–67.

Krubitzer L, Huffman KJ (2000) Arealization of the neocortex in mammals: Genetic and epigenetic contributions to the phenotype. Brain Behav Evol 55:322–335.

Krubitzer L, Huffman KJ, Disbrow E, Recanzone G (2004) Organization of area 3a in macaque monkeys: Contributions to the cortical phenotype. J Comp Neurol 471:97–111.

Krubitzer L, Campi KL, Cooke DF (2011) All rodents are not the same: A modern synthesis of cortical organization. Brain Behav Evol 78:51–93.

Kulkarni NH, Yamamoto AH, Robinson KO, Mackay TFC, Anholt RRH (2002) The DSC1 channel, encoded by the smi60E locus, contributes to odor-guided behavior in Drosophila melanogaster. Genetics 161:1507–1516.

Kumar S (2005) Molecular clocks: Four decades of evolution. Nat Rev Genet 6:654–662.

Ladich F, Bass AH (1998) Sonic/vocal motor pathways in catfishes: Comparisons with other teleosts. Brain Behav Evol 51:315–330.

Ladich F, Bass AH (2005) Sonic motor pathways in piranhas with a reassessment of phylogenetic patterns of sonic mechanisms among teleosts. Brain Behav Evol 66:167–176.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Ladich F, Fine ML (1992) Localization of pectoral fin motoneurons (sonic and hovering) in the croaking gourami Trichopsis vittatus. Brain Behav Evol 39:1–7.

Ladich F, Fine ML (1994) Localization of swimbladder and pectoral motoneurons involved in sound production in pimelodid catfish. Brain Behav Evol 44:86–100.

Ladich F, Fine ML (2006) Sound-generating mechanisms in fishes: A unique diversity in vertebrates. In Communication in Fishes, eds Ladich F, Collin SP, Moller P, Kapoor BG (Science Publishers, Enfield, NH), Vol 1, pp 3–43.

Ladich F, Tadler A (1988) Sound production in polypterus (Osteichthyes: Polypteridae). Copeia (4):1076–1077.

Ladich F, Brittinger W, Kratochvil H (1992) Significance of agonistic vocalization in the croaking gourami (Trichopsis vittatus, teleostei). Ethology 90:307–314.

Ladich F, Collin S, Moller P, Kapoor BG (2006) Communication in Fishes (Science Publishers, Enfield, NH).

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (2001) A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413:519–523.

Lai CSL, Gerrelli D, Monaco AP, Fisher SE, Copp AJ (2003) FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain 126:2455–2462.

Lakatos P, O’Connell MN, Barczak A, Mills A, Javitt DC, Schroeder CE (2009) The leading sense: Supramodal control of neurophysiological context by attention. Neuron 64:419–430.

Lakhdar-Ghazal N, Dubois Dauphin M, Hermes MLHJ, Buijs RM, Bengelloun, WA, Pevet P (1995) Vasopressin in the brain of a desert hibernator, the jerboa (Jaculus orientalis): Presence of sexual dimorphism and seasonal variation. J Comp Neurol 358:499–517.

Laland KN, Odling-Smee J, Feldman MW (2000) Niche construction, biological evolution, and cultural change. Behav Brain Sci 23:131–146.

Lalli CM, Gilmer RW (1989) Pelagic Snails (Stanford Univ Press, Stanford, CA).

Lance JR (1968) New panamic nudibranchs (Gastropoda: Opisthobranchia) from the Gulf of California. Trans San Diego Soc Nat Hist 15:3–13, pls 1–2.

Landgraf M, Thor S (2006) Development of Drosophila motoneurons: Specification and morphology. Semin Cell Dev Biol 17:3–11.

Lauder GV (1986) Homology, analogy, and the evolution of behavior. In Evolution of Animal Behavior, eds Nitecki MH, Kitchell JA (Oxford Univ Press, New York), pp 9–40.

Lauder GV (1994) Homology, form, and function. In Homology: The Hierachical Basis of Comparative Biology, ed Hall BK (Academic Press, San Diego), pp 151–196.

LaVail JH, Cowan WM (1971a) The development of the chick optic tectum. I. Normal morphology and cytoarchitectonic development. Brain Res 28:391–419.

LaVail JH, Cowan WM (1971b) The development of the chick optic tectum. II. Autoradiographic studies. Brain Res 28:421–441.

Lavenex P, Schenk F (1996) Integration of olfactory information in a spatial representation enabling accurate arm choice in the radial arm maze. Learn Mem 2:299–319.

Lawrence KA, Watson WH, 3rd (2002) Swimming behavior of the nudibranch Melibe leonina. Biol Bull 203:144–151.

Layden MJ, Boekhout M, Martindale MQ (2012) Nematostella vectensis achaete-scute homolog NvashA regulates embryonic ectodermal neurogenesis and represents an ancient component of the metazoan neural specification pathway. Development 139:1013–1022.

Le Corre M, Carey S (2007) One, two, three, four, nothing more: An investigation of the conceptual sources of the verbal counting principles. Cognition 105:395–438.

Lee JH, Russ BE, Orr LE, Cohen YE (2009) Prefrontal activity predicts monkeys’ decisions during an auditory category task. Front Integr Neurosci 3:16.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Lee M-J, Jeong DY, Kim WS, Kim HD, Kim CH, Park WW, Park YH, Kim KS, Kim HM, Kim DS (2000) A tetrodotoxin-producing Vibrio strain, LM-1, from the puffer fish Fugu vermicularis radiatus. Appl Environ Microbiol 66:1698–1701.

Lehtonen J, Kokko H (2012) Positive feedback and alternative stable states in inbreeding, cooperation, sex roles and other evolutionary processes. Philos Trans R Soc Lond B Biol Sci 367:211–221.

Leingärtner A, Thuret S, Kroll TT, Chou SJ, Leasure JL, Gage FH, O’Leary DD (2007) Cortical area size dictates performance at modality-specific behaviors. Proc Natl Acad Sci USA 104:4153–4158.

Lemons D, McGinnis W (2006) Genomic evolution of Hox gene clusters. Science 313:1918–1922.

Leung CH, Abebe D, Earp SE, Goode CT, Grozhik AV, Minidoddi P, Maney DL (2011) Neural distribution of vasotocin receptor mRNA in two species of songbird. Endocrinology 152:4865–4881.

Lewis EB (1978) A gene complex controlling segmentation in Drosophila. Nature 276:565–570.

Lewis OJ (1977) Joint remodelling and the evolution of the human hand. J Anat 123:157–201.

Leyton ASF, Sherrington CS (1917) Observations on the excitable cortex of the chimpanzee, orangutan, and gorilla. Q J Exp Physiol 11:137–222.

Li G, Wang J, Rossiter SJ, Jones G, Zhang S (2007) Accelerated FoxP2 evolution in echolocating bats. PLoS ONE 2:e900.

Li H, Richardson WD (2008) The evolution of Olig genes and their roles in myelination. Neuron Glia Biol 4:129–135.

Li Y, Fitzpatrick D, White LE (2006) The development of direction selectivity in ferret visual cortex requires early visual experience. Nat Neurosci 9:676–681.

Liebal K, Call J (2012) The origins of non-human primates’ manual gestures. Philos Trans R Soc Lond B Biol Sci 367:118–128.

Lieberman P (2006) Toward an Evolutionary Biology of Language (Harvard Univ Press, Cambridge, MA).

Liebeskind BJ (2011) Evolution of sodium channels and the new view of early nervous system evolution. Commun Integr Biol 4:679–683.

Liebeskind BJ, Hillis DM, Zakon HH (2011) Evolution of sodium channels predates the origin of nervous systems in animals. Proc Natl Acad Sci USA 108:9154–9159.

Liégeois F, Baldeweg T, Connelly A, Gadian DG, Mishkin M, Vargha-Khadem F (2003) Language fMRI abnormalities associated with FOXP2 gene mutation. Nat Neurosci 6:1230–1237.

Liégeois F, Morgan AT, Connelly A, Vargha-Khadem F (2011) Endophenotypes of FOXP2: Dysfunction within the human articulatory network. Eur J Paediatr Neurol 15:283–288.

Lillvis JL, Gunaratne CA, Katz PS (2012) Neurochemical and neuroanatomical identification of central pattern generator neuron homologues in Nudipleura molluscs. PLoS ONE 7:e31737.

Lipkind GM, Fozzard HA (2008) Voltage-gated Na channel selectivity: The role of the conserved domain III lysine residue. J Gen Physiol 131:523–529.

Lipton JS, Spelke ES (2005) Preschool children’s mapping of number words to nonsymbolic numerosities. Child Dev 76:978–988.

Liu JP, Laufer E, Jessell TM (2001) Assigning the positional identity of spinal motor neurons: Rostrocaudal patterning of Hox-c expression by FGFs, Gdf 11, and retinoids. Neuron 32:997–1012.

Liu Y, Curtis JT, Wang Z (2001) Vasopressin in the lateral septum regulates pair bond formation in male prairie voles (Microtus ochrogaster). Behav Neurosci 115:910–919.

Liu Z, Valles SM, Dong K (2000) Novel point mutations in the German cockroach para sodium channel gene are associated with knockdown resistance (kdr) to pyrethroid insecticides. Insect Biochem Mol Biol 30:991–997.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Liu Z, Li S, Wang W, Xu D, Murphy RW, Shi P (2011) Parallel evolution of KCNQ4 in echolocating bats. PLoS ONE 6:e26618.

Liubicich DM, Serano JM, Pavlopoulos A, Kontarakis Z, Protas ME, Kwan E, Chatterjee S, Tran KD, Averof M, Patel NH (2009) Knockdown of Parhyale Ultrabithorax recapitulates evolutionary changes in crustacean appendage morphology. Proc Natl Acad Sci USA 106:13892–13896.

Livingstone MS, Hubel DH (1984) Anatomy and physiology of a color system in the primate visual cortex. J Neurosci 4:309–356.

Livingstone M, Hubel D (1988) Segregation of form, color, movement, and depth: Anatomy, physiology, and perception. Science 240:740–749.

Lledo P-M, Alonso M, Grubb MS (2006) Adult neurogenesis and functional plasticity in neuronal circuits. Nat Rev Neurosci 7:179–193.

Llinás R, Paré D (1994) Role of intrinsic neuronal oscillations and network ensembles in the genesis of normal and pathological tremors. In Handbook of Tremor Disorders, eds Findley LJ, Koller WC (Marcel Dekker, New York), pp 7–36.

Llinás R, Yarom Y (1981) Electrophysiology of mammalian inferior olivary neurones in vitro. Different types of voltage-dependent ionic conductances. J Physiol 315:549–567.

Llinás R, Yarom Y (1986) Oscillatory properties of guinea-pig inferior olivary neurones and their pharmacological modulation: An in vitro study. J Physiol 376:163–182.

Llinás R, Baker R, Sotelo C (1974) Electrotonic coupling between neurons in cat inferior olive. J Neurophysiol 37:560–571.

Lobel PS, Kaatz IM, Rice AN (2010) Acoustical behavior of coral reef fishes. In Reproduction and Sexuality in Marine Fishes: Evolutionary Patterns and Innovations, ed Cole KS (Elsevier, San Diego), pp 307–386.

Lohmann KJ, Lohmann CMF (1996) Orientation and open-sea navigation in sea turtles. J Exp Biol 199:73–81.

López JC, Vargas JP, Gómez Y, Salas C (2003) Spatial and non-spatial learning in turtles: The role of medial cortex. Behav Brain Res 143:109–120.

Lopreato GF, Lu Y, Southwell A, Atkinson NS, Hillis DM, Wilcox TP, Zakon HH (2001) Evolution and divergence of sodium channel genes in vertebrates. Proc Natl Acad Sci USA 98:7588–7592.

Lorenz K (1981) The Foundations of Ethology (Springer-Verlag, New York).

Lourenco SF, Longo MR (2010) General magnitude representation in human infants. Psychol Sci 21:873–881.

Lourenco SF, Longo MR (2011) Origins and development of generalized magnitude representation. In Space, Time and Number in the Brain: Searching for the Foundations of Mathematical Thought, eds Dehaene S, Brannon E (Academic Press, London), 1st Ed, pp 225–244.

Love GD, Grosjean E, Stalvies C, Fike DA, Grotzinger JP, Bradley AS, Kelly AE, Bhatia M, Meredith W, Snape CE, Bowring SA, Condon DJ, Summons RE (2009) Fossil steroids record the appearance of Demospongiae during the Cryogenian period. Nature 457:718–721.

Lovejoy DA, Balment RJ (1999) Evolution and physiology of the corticotropin-releasing factor (CRF) family of neuropeptides in vertebrates. Gen Comp Endocrinol 115:1–22.

Lowe CJ (2008) Molecular genetic insights into deuterostome evolution from the direct-developing hemichordate Saccoglossus kowalevskii. Philos Trans R Soc Lond B Biol Sci 363:1569–1578.

Lowe CJ, Wu M, Salic A, Evans L, Lander E, Stange-Thomann N, Gruber CE, Gerhart J, Kirschner M (2003) Anteroposterior patterning in hemichordates and the origins of the chordate nervous system. Cell 113:853–865.

Lowe RT (1842) Description of a new dorsibranchiate gasteropod discovered at Madeira. Proc Zool Soc Lond 10:51–53.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Lu HD, Roe AW (2007) Optical imaging of contrast response in Macaque monkey V1 and V2. Cereb Cortex 17:2675–2695.

Lu HD, Roe AW (2008) Functional organization of color domains in V1 and V2 of macaque monkey revealed by optical imaging. Cereb Cortex 18:516–533.

Lumsden A, Keynes R (1989) Segmental patterns of neuronal development in the chick hindbrain. Nature 337:424–428.

Luo AH, Tahsili-Fahadan P, Wise RA, Lupica CR, Aston-Jones G (2011) Linking context with reward: A functional circuit from hippocampal CA3 to ventral tegmental area. Science 333:353–357.

Ma L-H, Punnamoottil B, Rinkwitz S, Baker R (2009) Mosaic hoxb4a neuronal pleiotropism in zebrafish caudal hindbrain. PLoS ONE 4:e5944.

Ma L-H, Gilland E, Bass AH, Baker R (2010) Ancestry of motor innervation to pectoral fin and forelimb. Nat Commun 1:49.

Ma PM (1991) The barrelettes—architectonic vibrissal representations in the brainstem trigeminal complex of the mouse. I. Normal structural organization. J Comp Neurol 309:161–199.

MacFarland FM (1966) Studies of Opisthobranchiate Mollusks of the Pacific Coast of North America (California Academy of Sciences, San Francisco).

Mackey SL, Kandel ER, Hawkins RD (1989) Identified serotonergic neurons LCB1 and RCB1 in the cerebral ganglia of Aplysia produce presynaptic facilitation of siphon sensory neurons. J Neurosci 9:4227–4235.

Macneil LT, Walhout AJ (2011) Gene regulatory networks and the role of robustness and stochasticity in the control of gene expression. Genome Res 21:645–657.

MacNeilage P (2008) The Origin of Speech (Oxford Univ Press, New York).

Mahon BZ, Cantlon JF (2011) The specialization of function: Cognitive and neural perspectives. Cogn Neuropsychol 28:147–155.

Malavasi S, Collatuzzo S, Torricelli P (2008) Interspecific variation of acoustic signals in Mediterranean gobies (Perciformes, Gobiidae): Comparative analysis and evolutionary outlook. Biol J Linn Soc Lond 93:763–778.

Mallatt J, Chen J, Holland ND (2003) Comment on “A new species of yunnanozoan with implications for deuterostome evolution.” Science 300:1372.

Maney DL, Ball GF (2003) Fos-like immunoreactivity in catecholaminergic brain nuclei after territorial behavior in free-living song sparrows. J Neurobiol 56:163–170.

Maney DL, Goodson JL (2011) Neurogenomic mechanisms of aggression in songbirds. Adv Genet 75:83–119.

Manger PR, Pettigrew JD (1996) Ultrastructure, number, distribution and innervation of electroreceptors and mechanoreceptors in the bill skin of the platypus, Ornithorhynchus anatinus. Brain Behav Evol 48:27–54.

Marasco PD, Catania KC (2007) Response properties of primary afferents supplying Eimer’s organ. J Exp Biol 210:765–780.

Marcus E (1955) Opisthobranchia from Brazil. Bol Fac Filos, Cien Letr Univ Sao Paulo, Zool 20:89–261, pls 1–30.

Marcus E, Marcus E (1962) Opisthobranchs from Florida and the Virgin Islands. Bull Mar Sci Gulf Caribbean 12:450–488.

Marcus E, Marcus E (1967) American Opisthobranch Molluscs (Univ Miami, Miami, FL).

Marcus GF (2004) The Birth of the Mind: How a Tiny Number of Genes Creates the Complexities of Human Thought (Basic Books, New York).

Marcus GF (2006) Cognitive architecture and descent with modification. Cognition 101: 443–465.

Margoliash E (1963) Primary structure and evolution of cytochrome C. Proc Natl Acad Sci USA 50:672–679.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Marino L (1998) A comparison of encephalization between odontocete cetaceans and anthropoid primates. Brain Behav Evol 51:230–238.

Marino L (2006) Absolute brain size: Did we throw the baby out with the bathwater? Proc Natl Acad Sci USA 103:13563–13564.

Markov NT, Ercsey-Ravasz MM, Gariel M-A, Dehay C, Knoblauch K, Toroczkai Z, Kennedy H (2011) The tribal networks of the cerebral cortex. In Cerebral Plasticity, eds Chalupa LM, Berardi N, Caleo M, Galli-Resta L, Pizzorusso T (MIT Press, Cambridge, MA), pp 275–290.

Marlow HQ, Srivastava M, Matus DQ, Rokhsar D, Martindale MQ (2009) Anatomy and development of the nervous system of Nematostella vectensis, an anthozoan cnidarian. Dev Neurobiol 69:235–254.

Marshall JG, Willan RC (1999) Nudibranchs of Heron Island, Great Barrier Reef—a Survey of the Opisthobranchia (Sea Slugs) of Heron and Wistari Reefs (Backhuys, Leiden, The Netherlands).

Martín C, Bueno D, Alonso MI, Moro JA, Callejo S, Parada C, Martín P, Carnicero E, Gato A (2006) FGF2 plays a key role in embryonic cerebrospinal fluid trophic properties over chick embryo neuroepithelial stem cells. Dev Biol 297:402–416.

Martin RP (1990) Primate Origins and Evolution: A Phylogenetic Reconstruction (Princeton Univ Press, Princeton, NJ).

Marzke MW, Marzke RF (2000) Evolution of the human hand: Approaches to acquiring, analysing and interpreting the anatomical evidence. J Anat 197:121–140.

Masel J, Trotter MV (2010) Robustness and evolvability. Trends Genet 26:406–414.

Matsumura K (1995) Tetrodotoxin as a pheromone. Nature 378:563–564.

Matthews SC, Missarzhevsky VV (1975) Small shelly fossils of late Precambrian and early Cambrian age: A review of recent work. J Geol Soc Lond 131:289–304.

Mayr E (1970) Populations, Species, and Evolution; An Abridgment of Animal Species and Evolution (Belknap, Cambridge, MA).

Mazzocco MM, Kover ST (2007) A longitudinal assessment of executive function skills and their association with math performance. Child Neuropsychol 13:18–45.

Mazzocco MMM, Singh Bhatia N, Lesniak-Karpiak K (2006) Visuospatial skills and their association with math performance in girls with fragile X or Turner syndrome. Child Neuropsychol 12:87–110.

McClellan AD, Brown GD, Getting PA (1994) Modulation of swimming in Tritonia: Excitatory and inhibitory effects of serotonin. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 174:257–266.

McCune AR, Schimenti JC (2012) Using genetic networks and homology to understand the evolution of phenotypic traits. Curr Genomics 13:74–84.

McGinnis W, Krumlauf R (1992) Homeobox genes and axial patterning. Cell 68:283–302.

McGowan L, Kuo E, Martin A, Monuki ES, Striedter G (2011) Species differences in early patterning of the avian brain. Evolution 65:907–911.

McGowan LD, Alaama RA, Freise AC, Huang JC, Charvet CJ, Striedter GF (2012) Expansion, folding, and abnormal lamination of the chick optic tectum after intraventricular injections of FGF2. Proc Natl Acad Sci USA 109(Suppl 1):10640-10646.

McGurk H, MacDonald JW (1976) Hearing lips and seeing voices. Nature 264:746–748.

McMenamin MAS (1998) The Garden of Ediacara (Columbia University Press, New York).

Means LW, Alexander SR, O’Neal MF (1992) Those cheating rats: Male and female rats use odor trails in a water-escape “working memory” task. Behav Neural Biol 58:144–151.

Meck WH, Church RM (1983) A mode control model of counting and timing processes. J Exp Psychol Anim Behav Process 9:320–334.

Medina L, Bupesh M, Abellán A (2011) Contribution of genoarchitecture to understanding forebrain evolution and development, with particular emphasis on the amygdala. Brain Behav Evol 78:216–236.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Menzel R, Greggers U, Smith A, Berger S, Brandt R, Brunke S, Bundrock G, Hülse S, Plümpe T, Schaupp F, Schüttler E, Stach S, Stindt J, Stollhoff N, Watzl S (2005) Honey bees navigate according to a map-like spatial memory. Proc Natl Acad Sci USA 102:3040–3045.

Menzel R, Kirbach A, Haass WD, Fischer B, Fuchs J, Koblofsky M, Lehmann K, Reiter L, Meyer H, Nguyen H, Jones S, Norton P, Greggers U (2011) A common frame of reference for learned and communicated vectors in honeybee navigation. Curr Biol 21:645–650.

Menzel R, Lehmann K, Manz G, Fuchs J (2012) Vector integration and novel shortcutting in honeybee navigation. Apidologie (Celle) 10.1007/s13592-012-0127-z.

Merzenich MM, Kaas JH (1980) Principles of organization of sensory-perceptual systems in mammals. In Progress in Psychobiology and Physiological Psychology, eds Sprague JM, Epstein AN (Academic Press, New York), pp 1–42.

Merzenich MM, Nelson RJ, Kaas JH, Stryker MP, Jenkins WM, Zook JM, Cynader MS, Schoppmann A (1987) Variability in hand surface representations in areas 3b and 1 in adult owl and squirrel monkeys. J Comp Neurol 258:281–296.

Meunier D, Achard S, Morcom A, Bullmore E (2009) Age-related changes in modular organization of human brain functional networks. Neuroimage 44:715–723.

Meyer A, Schartl M (1999) Gene and genome duplications in vertebrates: The one-to-four (-to-eight in fish) rule and the evolution of novel gene functions. Curr Opin Cell Biol 11:699–704.

Meyer E, Aglyamova GV, Matz MV (2011) Profiling gene expression responses of coral larvae (Acropora millepora) to elevated temperature and settlement inducers using a novel RNA-Seq procedure. Mol Ecol 20:3599–3616.

Miguel-Aliaga I, Thor S (2004) Segment-specific prevention of pioneer neuron apoptosis by cell-autonomous, postmitotic Hox gene activity. Development 131:6093–6105.

Miller EH, Baker AJ (2009) Antiquity of shorebird acoustic displays. Auk 126:454–459.

Miller EK, Cohen JD (2001) An integrative theory of prefrontal cortex function. Annu Rev Neurosci 24:167–202.

Miller EK, Freedman DJ, Wallis JD (2002) The prefrontal cortex: Categories, concepts and cognition. Philos Trans R Soc Lond B Biol Sci 357:1123–1136.

Miller LM, D’Esposito M (2005) Perceptual fusion and stimulus coincidence in the cross-modal integration of speech. J Neurosci 25:5884–5893.

Millot J, Anthony J (1965) Anatomie de Latimeria chalumnae. System Nerveux et Organes des Sens (Centre National de Recherche Scientifique, Paris).

Mills CE (1994) Seasonal swimming of sexually mature benthic opisthobranch molluscs (Melibe leonina and Gastropteron pacificum) may augment population dispersal. In Reproduction and Development of Marine Invertebrates, eds Wilson WH, Jr, Stricker SA, Shinn GL (Johns Hopkins Univ Press, Baltimore, MD), pp 313–319.

Mishkin M, Manning FJ (1978) Non-spatial memory after selective prefrontal lesions in monkeys. Brain Res 143:313–323.

Moczek AP, Cruickshank TE, Shelby A (2006) When ontogeny reveals what phylogeny hides: Gain and loss of horns during development and evolution of horned beetles. Evolution 60:2329–2341.

Molko N, Cachia A, Rivière D, Mangin JF, Bruandet M, Le Bihan D, Cohen L, Dehaene S (2003) Functional and structural alterations of the intraparietal sulcus in a developmental dyscalculia of genetic origin. Neuron 40:847–858.

Mondloch CJ, Maurer D (2004) Do small white balls squeak? Pitch-object correspondences in young children. Cogn Affect Behav Neurosci 4:133–136.

Montgomery SH, Capellini I, Venditti C, Barton RA, Mundy NI (2011) Adaptive evolution of four microcephaly genes and the evolution of brain size in anthropoid primates. Mol Biol Evol 28:625–638.

Morel A, Garraghty PE, Kaas JH (1993) Tonotopic organization, architectonic fields, and connections of auditory cortex in macaque monkeys. J Comp Neurol 335:437–459.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Morin-Kensicki EM, Melancon E, Eisen JS (2002) Segmental relationship between somites and vertebral column in zebrafish. Development 129:3851–3860.

Moroz LL (2009) On the independent origins of complex brains and neurons. Brain Behav Evol 74:177–190.

Mota B, Herculano-Houzel S (2012) How the cortex gets its folds: An inside-out, connectivity-driven model for the scaling of Mammalian cortical folding. Front Neuroanat 6:3.

Mountcastle VB (1957) Modality and topographic properties of single neurons of cat’s somatic sensory cortex. J Neurophysiol 20:408–434.

Mountcastle VB (1997) The columnar organization of the neocortex. Brain 120:701–722.

Mountcastle VB (2003) Introduction. Computation in cortical columns. Cereb Cortex 13: 2–4.

Mouret A, Lepousez G, Gras J, Gabellec MM, Lledo PM (2009) Turnover of newborn olfactory bulb neurons optimizes olfaction. J Neurosci 29:12302–12314.

Mukai M, Replogle K, Drnevich J, Wang G, Wacker D, Band M, Clayton DF, Wingfield, JC (2009) Seasonal differences of gene expression profiles in song sparrow (Melospiza melodia) hypothalamus in relation to territorial aggression. PLoS ONE 4:e8182.

Murakami Y, Pasqualetti M, Takio Y, Hirano S, Rijli FM, Kuratani S (2004) Segmental development of reticulospinal and branchiomotor neurons in lamprey: Insights into the evolution of the vertebrate hindbrain. Development 131:983–995.

Murphy JC (2007) Homalopsid Snakes, Evolution in the Mud (Kreiger, Melbourne).

Murphy WJ, Pevzner PA, O’Brien SJ (2004) Mammalian phylogenomics comes of age. Trends Genet 20:631–639.

Murthy VN (2011) Olfactory maps in the brain. Annu Rev Neurosci 34:233–258.

Myers N, Mittermeier RA, Mittermeier CG, da Fonseca GA, Kent J (2000) Biodiversity hotspots for conservation priorities. Nature 403:853–858.

National Center for Biotechnology Information. Forkhead box P2 (FOXP2). UGID: 176333; UniGene Hs.282787, Homo sapiens (human) FOXP2. Available at http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=282787&MAXEST=94. Accessed February 19, 2012.

Neafsey EJ, Bold EL, Haas G, Hurley-Gius KM, Quirk G, Sievert CF, Terreberry RR (1986) The organization of the rat motor cortex: A microstimulation mapping study. Brain Res 396:77–96.

Nederbragt AJ, te Welscher P, van den Driesche S, van Loon AE, Dictus WJAG (2002) Novel and conserved roles for orthodenticle/otx and orthopedia/otp orthologs in the gastropod mollusc Patella vulgata. Dev Genes Evol 212:330–337.

Nelson JS (2006) Fishes of the World (Wiley, New York), 4th Ed.

Nelson RJ, Sur M, Felleman DJ, Kaas JH (1980) Representations of the body surface in postcentral parietal cortex of Macaca fascicularis. J Comp Neurol 192:611–643.

Nemec P, Cveková P, Benada O, Wielkopolska E, Olkowicz S, Turlejski K, Burda H, Bennett NC, Peichl L (2008) The visual system in subterranean African mole-rats (Rodentia, Bathyergidae): Retina, subcortical visual nuclei and primary visual cortex. Brain Res Bull 75:356–364.

Neu W (1932) Wie schwimmt Aplysia depilans L. Zeitschr Vergl Physiol 18:244–254.

Nevitt GA (2008) Sensory ecology on the high seas: The odor world of the procellariiform seabirds. J Exp Biol 211:1706–1713.

Newcomb JM, Katz PS (2007) Homologues of serotonergic central pattern generator neurons in related nudibranch molluscs with divergent behaviors. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 193:425–443.

Newcomb JM, Katz PS (2009) Different functions for homologous serotonergic interneurons and serotonin in species-specific rhythmic behaviours. Proc Biol Sci 276:99–108.

Newman JD, Lindsley DF (1976) Single unit analysis of auditory processing in squirrel monkey frontal cortex. Exp Brain Res 25:169–181.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Newman MEJ (2006) Finding community structure in networks using the eigenvectors of matrices. Phys Rev E Stat Nonlin Soft Matter Phys 74:036104.

Newman SW (1999) The medial extended amygdala in male reproductive behavior. A node in the mammalian social behavior network. Ann N Y Acad Sci 877:242–257.

Nieder A (2005) Counting on neurons: The neurobiology of numerical competence. Nat Rev Neurosci 6:177–190.

Nieder A (2009) Prefrontal cortex and the evolution of symbolic reference. Curr Opin Neurobiol 19:99–108.

Nieder A, Miller EK (2003) Coding of cognitive magnitude: Compressed scaling of numerical information in the primate prefrontal cortex. Neuron 37:149–157.

Nieder A, Miller EK (2004) A parieto-frontal network for visual numerical information in the monkey. Proc Natl Acad Sci USA 101:7457–7462.

Nieder A, Freedman DJ, Miller EK (2002) Representation of the quantity of visual items in the primate prefrontal cortex. Science 297:1708–1711.

Niedermeyer E (2005) Historical aspects. In Electroencephalography: Basic Principles, Clinical Applications, and Related Fields, eds Niedermeyer E, Lopes Da Silva FH (Lippincott Williams & Wilkins, Philadelphia, PA), pp 1–15.

Nieuwenhuys R (1994a) Comparative neuroanatomy: Place, principles, practice and programme. Europ J Morphol 32:142–155.

Nieuwenhuys R (1994b) The neocortex. An overview of its evolutionary development, structural organization and synaptology. Anat Embryol (Berl) 190:307–337.

Nieuwenhuys R, Donkelaar HJ, Nicholson C (1998) The Central Nervous System of Vertebrates (Springer, Berlin).

Niimura Y (2009) Evolutionary dynamics of olfactory receptor genes in chordates: Interaction between environments and genomic contents. Hum Genomics 4:107–118.

Nishita J, Ohta S, Bleyl SB, Schoenwolf GC (2011) Detection of isoform-specific fibroblast growth factor receptors by whole-mount in situ hybridization in early chick embryos. Dev Dyn 240:1537–1547.

Nishiyama A, Yang Z, Butt A (2005) Astrocytes and NG2-glia: What’s in a name? J Anat 207:687–693.

Noda A, Ohba H, Kakiuchi T, Futatsubashi M, Tsukada H, Nishimura S (2002) Age-related changes in cerebral blood flow and glucose metabolism in conscious rhesus monkeys. Brain Res 936:76–81.

Noden DM, Francis-West P (2006) The differentiation and morphogenesis of craniofacial muscles. Dev Dyn 235:1194–1218.

Nolan V, Jr, Ketterson ED, Cristol DA, Rogers CM, Clotfelter ED, Titus RC, Schoech SJ, Snajdr E (2002) Dark-eyed junco (Junco hyemalis). Birds North Am 716:1–44.

Noll M (1993) Evolution and role of Pax genes. Curr Opin Genet Dev 3:595–605.

Noppeney U, Ostwald D, Werner S (2010) Perceptual decisions formed by accumulation of audiovisual evidence in prefrontal cortex. J Neurosci 30:7434–7446.

Northcutt RG (1984) Evolution of the vertebrate central nervous system: Patterns and processes. Am Zool 24:701–716.

Northcutt RG (1985) The brain and sense organs of the earliest vertebrates: Reconstruction of a morphotype. In Evolutionary Biology of Primitive Fishes, eds Foreman RE, Gorbaman A, Dodd JM, Olssen R (Plenum, New York).

Northcutt RG (1990) Ontogeny and phylogeny: A re-evaluation of conceptual relationships and some applications. Brain Behav Evol 36:116–140.

Northcutt RG (2003) Origin of the isthmus? A comparison of the brains of lancelets and vertebrates. J Comp Neurol 466:316–318.

Northcutt RG, Bemis WE (1993) Cranial nerves of the coelacanth, Latimeria chalumnae [Osteichthyes: Sarcopterygii: Actinistia], and comparisons with other craniata. Brain Behav Evol 42(Suppl 1):1–76.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Northcutt RG, Gans C (1983) The genesis of neural crest and epidermal placodes: A reinterpretation of vertebrate origins. Q Rev Biol 58:1–28.

Nottebohm F, Liu WC (2010) The origins of vocal learning: New sounds, new circuits, new cells. Brain Lang 115:3–17.

Nottebohm F, Stokes TM, Leonard CM (1976) Central control of song in the canary, Serinus canarius. J Comp Neurol 165:457–486.

Novak AE, Jost MC, Lu Y, Taylor AD, Zakon HH, Ribera AB (2006) Gene duplications and evolution of vertebrate voltage-gated sodium channels. J Mol Evol 63:208–221.

Nunn CL (2011) The Comparative Approach in Evolutionary Anthropology and Biology (Univ of Chicago Press, Chicago).

Nüsslein-Volhard C, Wieschaus E (1980) Mutations affecting segment number and polarity in Drosophila. Nature 287:795–801.

Nuttall GHF (1904) Blood Immunity and Blood Relationships (Cambridge Univ Press, Cambridge, UK).

Obayashi S, Spengler S, Simons JS, Steele JD, Lawrie SM, Frith CD, Burgess PW (2001) Functional brain mapping of monkey tool use. Neuroimage 14:853–861.

Ogiwara I, Miyamoto H, Morita N, Atapour N, Mazaki E, Inoue I, Takeuchi T, Itohara S, Yanagawa Y, Obata K, Furuichi T, Hensch TK, Yamakawa K (2007) Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: A circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation. J Neurosci 27:5903–5914.

Ohmiya M, Fukumitsu H, Nitta A, Nomoto H, Furukawa Y, Furukawa S (2001) Administration of FGF-2 to embryonic mouse brain induces hydrocephalic brain morphology and aberrant differentiation of neurons in the postnatal cerebral cortex. J Neurosci Res 65:228–235.

Ohno S (1970) Evolution by Gene Duplication (Springer-Verlag, New York).

Ojanen V, Möttönen R, Pekkola J, Jääskeläinen IP, Joensuu R, Autti T, Sams M (2005) Processing of audiovisual speech in Broca’s area. Neuroimage 25:333–338.

Oldham MC, Horvath S, Geschwind DH (2006) Conservation and evolution of gene coexpression networks in human and chimpanzee brains. Proc Natl Acad Sci USA 103:17973–17978.

Oldham MC, Konopka G, Iwamoto K, Langfelder P, Kato T, Horvath S, Geschwind DH (2008) Functional organization of the transcriptome in human brain. Nat Neurosci 11:1271–1282.

O’Leary DD, Sahara S (2008) Genetic regulation of arealization of the neocortex. Curr Opin Neurobiol 18:90–100.

O’Leary DDM, Chou S-J, Sahara S (2007) Area patterning of the mammalian cortex. Neuron 56:252–269.

Onuki A, Somiya H (2007) Innervation of sonic muscles in teleosts: Occipital vs. spinal nerves. Brain Behav Evol 69:132–141.

Ophir AG, Zheng DJ, Eans S, Phelps SM (2009) Social investigation in a memory task relates to natural variation in septal expression of oxytocin receptor and vasopressin receptor 1a in prairie voles (Microtus ochrogaster). Behav Neurosci 123:979–991.

Ó Scalaidhe SP, Wilson FA, Goldman-Rakic PS (1997) Areal segregation of face-processing neurons in prefrontal cortex. Science 278:1135–1138.

Ó Scalaidhe SP, Wilson FAW, Goldman-Rakic PS (1999) Face-selective neurons during passive viewing and working memory performance of rhesus monkeys: Evidence for intrinsic specialization of neuronal coding. Cereb Cortex 9:459–475.

Osorio D, Getz WM, Rybak J (1994) Insect vision and olfaction: different neural architectures for different kinds of sensory signal? In From Animals to Animats 3: Proceedings of the Third International Conference on Simulation of Adaptive Behavior, eds Clift D, Husbands P, Meyer J-A, Wilson SW (MIT Press, Cambridge, MA), pp 73–81.

Ostergaard JM (1955) Some Opisthobranch mollusca from Hawaii. Pac Sci 9:110–136.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Otto SJ, McCorkle SR, Hover J, Conaco C, Han JJ, Impey S, Yochum GS, Dunn JJ, Goodman RH, Mandel G (2007) A new binding motif for the transcriptional repressor REST uncovers large gene networks devoted to neuronal functions. J Neurosci 27:6729–6739.

Owen R (1859) Contributions to the natural history of the anthropoid apes. No VIII. On the external characters of the Gorilla (Troglodytes gorilla Sav.). Trans Zool Soc 5:243–283.

Owen-Smith NR (1988) Megaherbivores (Cambridge Univ Press, Cambridge, UK).

Pace S (1901) On the rediscovery of Euselenops [=Neda] luniceps (Cuv.). J Mollusc Stud 4: 202–204.

Padberg J, Disbrow E, Krubitzer L (2005) The organization and connections of anterior and posterior parietal cortex in titi monkeys: Do New World monkeys have an area 2? Cereb Cortex 15:1938–1963.

Padberg J, Franca JG, Cooke DF, Soares JG, Rosa MG, Fiorani M Jr, Gattass R, Krubitzer L (2007) Parallel evolution of cortical areas involved in skilled hand use. J Neurosci 27:10106–10115.

Panchin YV, Popova LB, Deliagina TG, Orlovsky GN, Arshavsky YI (1995) Control of locomotion in marine mollusk Clione limacina. VIII. Cerebropedal neurons. J Neurophysiol 73:1912–1923.

Pandya DN, Hallett M, Kmukherjee SK (1969) Intra- and interhemispheric connections of the neocortical auditory system in the rhesus monkey. Brain Res 14:49–65.

Park TJ, Lu Y, Jüttner R, Smith ES, Hu J, Brand A, Wetzel C, Milenkovic N, Erdmann B, Heppenstall PA, Laurito CE, Wilson SP, Lewin GR (2008) Selective inflammatory pain insensitivity in the African naked mole-rat (Heterocephalus glaber). PLoS Biol 6:e13.

Parmentier E, Vandewalle P, Brié C, Dinraths L, Lecchini D (2011) Comparative study on sound production in different Holocentridae species. Front Zool 8:12.

Passingham RE (2008) What Is Special About the Human Brain? (Oxford Univ Press, New York).

Passingham RE, Toni I, Rushworth MF (2000) Specialisation within the prefrontal cortex: The ventral prefrontal cortex and associative learning. Exp Brain Res 133:103–113.

Pastor AM, De la Cruz RR, Baker R (1994) Eye position and eye velocity integrators reside in separate brainstem nuclei. Proc Natl Acad Sci USA 91:807–811.

Patterson C (1982) Morphological characters and homology. In Problems of Phylogenetic Reconstruction, eds Joysey KA, Friday AE (Academic Press, London), pp 21–74.

Paulesu E, Frith CD, Frackowiak RSJ (1993) The neural correlates of the verbal component of working memory. Nature 362:342–345.

Pavlopoulos A, Kontarakis Z, Liubicich DM, Serano JM, Akam M, Patel NH, Averof M (2009) Probing the evolution of appendage specialization by Hox gene misexpression in an emerging model crustacean. Proc Natl Acad Sci USA 106:13897–13902.

Paxinos G, Huang X, Toga AW (2000) The Rhesus Monkey Brain (Academic Press, San Diego).

Pearson BJ, Doe CQ (2004) Specification of temporal identity in the developing nervous system. Annu Rev Cell Dev Biol 20:619–647.

Pease WH (1860) Descriptions of a new species of mollusca from the Sandwich Islands, Part 1. Proc Zool Soc Lond 28:36.

Penn DC, Holyoak KJ, Povinelli DJ (2008) Darwin’s mistake: Explaining the discontinuity between human and nonhuman minds. Behav Brain Sci 31:109–130.

Perez Velazquez JL, Carlen PL (2000) Gap junctions, synchrony and seizures. Trends Neurosci 23:68–74.

Perseke M, Hankeln T, Weich B, Fritzsch G, Stadler PF, Israelsson O, Bernhard D, Schlegel M. (2007) The mitochondrial DNA of Xenoturbella bocki: Genomic architecture and phylogenetic analysis. Theory Biosci 126:35–42.

Peter IS, Davidson EH (2011) Evolution of gene regulatory networks controlling body plan development. Cell 144:970–985.

Peterson C, Carney GE, Taylor BJ, White K (2002) Reaper is required for neuroblast apoptosis during Drosophila development. Development 129:1467–1476.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Peterson KJ, Butterfield NJ (2005) Origin of the Eumetazoa: Testing ecological predictions of molecular clocks against the Proterozoic fossil record. Proc Natl Acad Sci USA 102:9547–9552.

Peterson KJ, Lyons JB, Nowak KS, Takacs CM, Wargo MJ, McPeek MA (2004) Estimating metazoan divergence times with a molecular clock. Proc Natl Acad Sci USA 101: 6536–6541.

Peterson KJ, Cotton JA, Gehling JG, Pisani D (2008) The Ediacaran emergence of bilaterians: Congruence between the genetic and the geological fossil records. Philos Trans R Soc Lond B Biol Sci 363:1435–1443.

Peterson RH (1975) Pectoral fin and opercular movements of Atlantic salmon (Salmo salar) alevins. J Fish Res Board Can 32:643–647.

Petrides M, Pandya DN (1988) Association fiber pathways to the frontal cortex from the superior temporal region in the rhesus monkey. J Comp Neurol 273:52–66.

Petrides M, Pandya DN (2002) Comparative cytoarchitectonic analysis of the human and the macaque ventrolateral prefrontal cortex and corticocortical connection patterns in the monkey. Eur J Neurosci 16:291–310.

Petrides M, Cadoret G, Mackey S (2005) Orofacial somatomotor responses in the macaque monkey homologue of Broca’s area. Nature 435:1235–1238.

Philippe H, Brinkmann H, Copley RR, Moroz LL, Nakano H, Poustka AJ, Wallberg A, Peterson KJ, Telford MJ (2011) Acoelomorph flatworms are deuterostomes related to Xenoturbella. Nature 470:255–258.

Piaget J (1952) The Child’s Conception of Number (Routledge & Paul, London), p ix.

Piazza M (2010) Neurocognitive start-up tools for symbolic number representations. Trends Cogn Sci 14:542–551.

Piazza M, Izard V, Pinel P, Le Bihan D, Dehaene S (2004) Tuning curves for approximate numerosity in the human intraparietal sulcus. Neuron. 44:547–555. Available at http://www.sciencedirect.com/science/journal/08966273.

Piazza M, Pinel P, Le Bihan D, Dehaene S (2007) A magnitude code common to numerosities and number symbols in human intraparietal cortex. Neuron 53:293–305.

Pica P, Lemer C, Izard V, Dehaene S (2004) Exact and approximate arithmetic in an Amazonian indigene group. Science 306:499–503.

Picton BE, Morrow CC (1994) A Field Guide to the Nudibranchs of the British Isles (Immel, London).

Pinel P, Piazza M, Le Bihan D, Dehaene S (2004) Distributed and overlapping cerebral representations of number, size, and luminance during comparative judgments. Neuron 41:983–993.

Pinker S (1994) The Language Instinct (Norton, New York).

Pinsk MA, DeSimone K, Moore T, Gross CG, Kastner S (2005) Representations of faces and body parts in macaque temporal cortex: A functional MRI study. Proc Natl Acad Sci USA 102:6996–7001.

Plotnick RE, Dornbos SQ, Chen J (2010) Information landscapes and sensory ecology of the Cambrian radiation. Paleobiology 36:303–317.

Pola M, Gosliner TM (2010) The first molecular phylogeny of cladobranchian opisthobranchs (Mollusca, Gastropoda, Nudibranchia). Mol Phylogenet Evol 56:931–941.

Pola M, Cervera JL, Gosliner TM (2006) Description of two new phanerobranch nembrothid species (Nudibranchia: Polyceridae: Doridacea). J Mar Biol Assoc U K 86:403–409.

Poldrack RA, Wagner AD, Prull MW, Desmond JE, Glover GH, Gabrieli JD (1999) Functional specialization for semantic and phonological processing in the left inferior prefrontal cortex. Neuroimage 10:15–35.

Pollard KS, Salama SR, Lambert N, Lambot MA, Coppens S, Pedersen JS, Katzman S, King B, Onodera C, Siepel A, Kern AD, Dehay C, Igel H, Ares M Jr, Vanderhaeghen P, Haussler D (2006) An RNA gene expressed during cortical development evolved rapidly in humans. Nature 443:167–172.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Pontes M (2002) Mediterranean nudibranchs: Marionia blainvillea. Nudibranch News 4:45–52.

Popescu IR, Frost WN (2002) Highly dissimilar behaviors mediated by a multifunctional network in the marine mollusk Tritonia diomedea. J Neurosci 22:1985–1993.

Poremba A, Mishkin M (2007) Exploring the extent and function of higher-order auditory cortex in rhesus monkeys. Hear Res 229:14–23.

Porter MA, Onnela J-P, Mucha PJ (2009) Communities in networks. Notices Am Math Soc 56:1082–1097.

Porter RK, Brand MD (1995a) Causes of differences in respiration rate of hepatocytes from mammals of different body mass. Am J Physiol 269(Pt 2):R1213–R1224.

Porter RK, Brand MD (1995b) Cellular oxygen consumption depends on body mass. Am J Physiol 269(Pt 2):R226–R228.

Povinelli DJ (1993) Reconstructing the evolution of mind. Am Psychol 48:493–509.

Povinelli DJ (2000) Folk Physics for Apes (Oxford Univ Press, New York).

Povinelli DJ (2012) World Without Weight: Perspectives on an Alien Mind (Oxford Univ Press, New York).

Povinelli DJ, Eddy TJ (1996) What young chimpanzees know about seeing. Monogr Soc Res Child Dev 61:1–152.

Premack D (2007) Human and animal cognition: Continuity and discontinuity. Proc Natl Acad Sci USA 104:13861–13867.

Premack D (2010) Why humans are unique: Three theories. Perspect Psychol Sci 5:22–32.

Preuss TM (1995) The argument from animals to humans in cognitive neuroscience. In The Cognitive Neurosciences, ed Gazzaniga MS (MIT Press, Cambridge, MA), pp 1227–1241.

Preuss TM (2001) The discovery of cerebral diversity: An unwelcome scientific revolution. In Evolutionary Anatomy of the Primate Cerebral Cortex, eds Falk D, Gibson K (Cambridge Univ Press, Cambridge, UK), pp 138–164.

Preuss TM (2007) Evolutionary specializations of primate brain systems. In Primate Origins: Adaptations and Evolution, eds Ravosa MJ, Dagosto M (Springer, New York), pp 625–675.

Preuss TM (2009) The cognitive neuroscience of human uniqueness. In The Cognitive Neurosciences, ed Gazzaniga MS (MIT Press, Cambridge, MA), 4th Ed, pp 49–64.

Preuss TM (2010) Reinventing primate neuroscience for the twenty-first century. In Primate Neuroethology, eds Platt ML, Ghazanfar AA (Oxford University Press, Oxford), pp 422–454.

Preuss TM (2011) The human brain: Rewired and running hot. Ann N Y Acad Sci 1225(Suppl 1):E182–E191.

Preuss TM (2012) Alien brains: A defense of exceptionalism. In World Without Weight: Perspectives on an Alien Mind, ed Povinelli D (Oxford Univ Press, Oxford), pp 30–31.

Preuss TM, Goldman-Rakic PS (1991) Myelo- and cytoarchitecture of the granular frontal cortex and surrounding regions in the strepsirhine primate Galago and the anthropoid primate Macaca. J Comp Neurol 310:429–474.

Zeiss atlas 9000 manual

Preuss TM, Kaas JH (1996) Cytochrome oxidase “blobs” and other characteristics of primary visual cortex in a lemuroid primate, Cheirogaleus medius. Brain Behav Evol 47: 103–112.

Preuss TM, Cáceres M, Oldham MC, Geschwind DH (2004) Human brain evolution: Insights from microarrays. Nat Rev Genet 5:850–860.

Price CJ (1998) The functional anatomy of word comprehension and production. Trends Cogn Sci 2:281–288.

Price GR, Holloway I, Räsänen P, Vesterinen M, Ansari D (2007) Impaired parietal magnitude processing in developmental dyscalculia. Curr Biol 17:R1042–R1043.

Price TD, Qvarnström A, Irwin DE (2003) The role of phenotypic plasticity in driving genetic evolution. Proc Biol Sci 270:1433–1440.

Prince VE, Moens CB, Kimmel CB, Ho RK (1998) Zebrafish hox genes: Expression in the hindbrain region of wild-type and mutants of the segmentation gene, valentino. Development 125:393–406.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Pritz MB (2005) Comparisons and homology in adult and developing vertebrate central nervous systems. Brain Behav Evol 66:222–233.

Proctor HC (1996) Measures of homoplasy. In Homoplasy: The Recurrence of Similarity in Evolution, eds Sanderson MJ, Hufford L (Academic Press, San Diego), pp 131–149.

Prokop A, Technau GM (1991) The origin of postembryonic neuroblasts in the ventral nerve cord of Drosophila melanogaster. Development 111:79–88.

Prokop A, Technau GM (1994) Early tagma-specific commitment of Drosophila CNS progenitor NB1-1. Development 120:2567–2578.

Prokop A, Bray S, Harrison E, Technau GM (1998) Homeotic regulation of segment-specific differences in neuroblast numbers and proliferation in the Drosophila central nervous system. Mech Dev 74:99–110.

Proske U, Gregory JE, Iggo A (1998) Sensory receptors in monotremes. Philos Trans R Soc Lond B Biol Sci 353:1187–1198.

Prothero J (1997) Scaling of cortical neuron density and white matter volume in mammals. J Hirnforsch 38:513–524.

Prothero JW, Sundsten JW (1984) Folding of the cerebral cortex in mammals. A scaling model. Brain Behav Evol 24:152–167.

Prum RO (1998) Sexual selection and the evolution of mechanical sound production in manakins (Aves: Pipridae). Anim Behav 55:977–994.

Pruvot-Fol A (1954) Mollusques opisthobranchs. Faune de France (Lechevalier, Paris).

Purves D, Riddle DR, LaMantia AS (1992) Iterated patterns of brain circuitry (or how the cortex gets its spots). Trends Neurosci 15:362–368.

Putman NF, Endres CS, Lohmann CMF, Lohmann KJ (2011) Longitude perception and bicoordinate magnetic maps in sea turtles. Curr Biol 21:463–466.

Qi HX, Kaas JH (2004) Myelin stains reveal an anatomical framework for the representation of the digits in somatosensory area 3b of macaque monkeys. J Comp Neurol 477:172–187.

Qi HX, Stepniewska I, Kaas JH (2000) Reorganization of primary motor cortex in adult macaque monkeys with long-standing amputations. J Neurophysiol 84:2133–2147.

Quackenbush J (2003) Genomics. Microarrays—guilt by association. Science 302:240–241.

Quartz SR, Sejnowski TJ (1997) The neural basis of cognitive development: A constructivist manifesto. Behav Brain Sci 20:537–556.

Quilliam TA (1966) The mole’s sensory apparatus. J Zool 149:76–88.

Quintana J, Fuster JM (1992) Mnemonic and predictive functions of cortical neurons in a memory task. Neuroreport 3:721–724.

Quiroga S, Ardila NE, Bolaños M (2004) Aphelodoris antillensis Berg, 1897 (Opisthobranchia: Nudibranchia: Dorididae), first record from the Colombian Caribbean. Bol Invest Mar Cost 33:229–231.

Raballo R, Rhee J, Lyn-Cook R, Leckman JF, Schwartz ML, Vaccarino FM (2000) Basic fibroblast growth factor (Fgf2) is necessary for cell proliferation and neurogenesis in the developing cerebral cortex. J Neurosci 20:5012–5023.

Radakovits R, Barros CS, Belvindrah R, Patton B, Müller U (2009) Regulation of radial glial survival by signals from the meninges. J Neurosci 29:7694–7705.

Raff RA (1996) The Shape of Life (Univ of Chicago Press, Chicago).

Rajimehr R, Young JC, Tootell RB (2009) An anterior temporal face patch in human cortex, predicted by macaque maps. Proc Natl Acad Sci USA 106:1995–2000.

Rakic P (1988) Specification of cerebral cortical areas. Science 241:170–176.

Rakic P (1995a) A small step for the cell, a giant leap for mankind: A hypothesis of neocortical expansion during evolution. Trends Neurosci 18:383–388.

Rakic P (1995b) Radial versus tangential migration of neuronal clones in the developing cerebral cortex. Proc Natl Acad Sci USA 92:11323–11327.

Rakic P (2009) Evolution of the neocortex: A perspective from developmental biology. Nat Rev Neurosci 10:724–735.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Ramnani N, Behrens TE, Johansen-Berg H, Richter MC, Pinsk MA, Andersson JL, Rudebeck P, Ciccarelli O, Richter W, Thompson AJ, Gross CG, Robson MD, Kastner S, Matthews PM (2006) The evolution of prefrontal inputs to the cortico-pontine system: Diffusion imaging evidence from macaque monkeys and humans. Cereb Cortex 16:811–818.

Rash BG, Grove EA (2006) Area and layer patterning in the developing cerebral cortex. Curr Opin Neurobiol 16:25–34.

Rauschecker JP, Scott SK (2009) Maps and streams in the auditory cortex: Nonhuman primates illuminate human speech processing. Nat Neurosci 12:718–724.

Rauschecker JP, Tian B, Hauser M (1995) Processing of complex sounds in the macaque nonprimary auditory cortex. Science 268:111–114.

Ray J, Gage FH (1994) Spinal cord neuroblasts proliferate in response to basic fibroblast growth factor. J Neurosci 14:3548–3564.

Redies C, Puelles L (2001) Modularity in vertebrate brain development and evolution. Bioessays 23:1100–1111.

Reep RL, Finlay BL, Darlington RB (2007) The limbic system in mammalian brain evolution. Brain Behav Evol 70:57–70.

Rehkämper G, Haase E, Frahm HD (1988) Allometric comparison of brain weight and brain structure volumes in different breeds of the domestic pigeon, Columba livia f.d. (fantails, homing pigeons, strassers). Brain Behav Evol 31:141–149.

Reichert H, Simeone A (2001) Developmental genetic evidence for a monophyletic origin of the bilaterian brain. Philos Trans R Soc Lond B Biol Sci 356:1533–1544.

Reidenberg JS (2007) Anatomical adaptations of aquatic mammals. Anat Rec (Hoboken) 290: 507–513.

Remage-Healey L, Bass AH (2004) Rapid, hierarchical modulation of vocal patterning by steroid hormones. J Neurosci 24:5892–5900.

Remage-Healey LH, Bass AH (2006) From social behavior to neurons: Rapid modulation of advertisement calling and vocal pattern generators by steroid hormones. Horm Behav 50:432–441.

Remedios R, Logothetis NK, Kayser C (2009) Monkey drumming reveals common networks for perceiving vocal and nonvocal communication sounds. Proc Natl Acad Sci USA 106:18010–18015.

Remple MS, Reed JL, Stepniewska I, Lyon DC, Kaas JH (2007) The organization of frontoparietal cortex in the tree shrew (Tupaia belangeri): II. Connectional evidence for a frontal-posterior parietal network. J Comp Neurol 501:121–149.

Rendall D, Di Fiore A (2007) Homoplasy, homology, and the perceived special status of behavior in evolution. J Hum Evol 52:504–521.

Reynolds V (1965) Some behavioral comparisons between the chimpanzee and the mountain gorilla in the wild. Am Anthropol 67:691–706.

Richards GS, Simionato E, Perron M, Adamska M, Vervoort M, Degnan BM (2008) Sponge genes provide new insight into the evolutionary origin of the neurogenic circuit. Curr Biol 18:1156–1161.

Richerson PJ, Boyd R (2006) Not by Genes Alone: How Culture Transformed Human Evolution (Univ Chicago Press, Chicago).

Riddle DR, Purves D (1995) Individual variation and lateral asymmetry of the rat primary somatosensory cortex. J Neurosci 15:4184–4195.

Rilling JK (2006) Human and nonhuman primate brains: Are they allometrically scaled versions of the same design? Evol Anthropol 15:65–77.

Rilling JK (2008) Neuroscientific approaches and applications within anthropology. Am J Phys Anthropol 137(Suppl 47):2–32.

Rilling JK, Insel TR (1999) The primate neocortex in comparative perspective using magnetic resonance imaging. J Hum Evol 37:191–223.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Rilling JK, Glasser MF, Preuss TM, Ma X, Zhao T, Hu X, Behrens TE (2008) The evolution of the arcuate fasciculus revealed with comparative DTI. Nat Neurosci 11:426–428.

Rilling JK, Glasser MF, Jbabdi S, Andersson J, Preuss TM (2011) Continuity, divergence, and the evolution of brain language pathways. Front Evol Neurosci 3:11.

Ringo JL (1991) Neuronal interconnection as a function of brain size. Brain Behav Evol 38: 1–6.

Risbec J (1925) Production de lumière par un mollusque nudibranche de la Nouvelle Calèdonie. Compt Rend Acad Sci Paris 181:472–473.

Risbec J (1928) Contribution a l’etude des nudibranches Neo-Caledoniens. Faune Colon Franç 2:11–328, pls 1–12.

Risbec J (1937) Note préliminaire au sujet de nudibranches Néo-Calédoniens. Bull Mus Natl Hist Nat Paris, Ser 2 9:159–164.

Risbec J (1953) Mollusques nudibranchs de la Nouvelle Calédonie. Faune Union Franç 15: 1–189.

Riska B, Atchley WR (1985) Genetics of growth predict patterns of brain-size evolution. Science 229:668–671.

Ritson-Williams R, Yotsu-Yamashita M, Paul VJ (2006) Ecological functions of tetrodotoxin in a deadly polyclad flatworm. Proc Natl Acad Sci USA 103:3176–3179.

Rivas E (2005) Recent use of signs by chimpanzees (Pan troglodytes) in interactions with humans. J Comp Psychol 119:404–417.

Rivera SM, Reiss AL, Eckert MA, Menon V (2005) Developmental changes in mental arithmetic: Evidence for increased functional specialization in the left inferior parietal cortex. Cereb Cortex 15:1779–1790.

Robilliard GA (1970) The systematics and some aspects of the ecology of the genus Dendronotus (Gastropoda: Nudibranchia). Veliger 12:433–479.

Robilliard GA (1972) A new species of Dendronotus from the northeastern Pacific with notes on Dendronotus nanus and Dendronotus robustus (Mollusca: Opisthobranchia). Can J Zool 50:421–432.

Rochefort C, He X, Scotto-Lomassese S, Scharff C (2007) Recruitment of FoxP2-expressing neurons to area X varies during song development. Dev Neurobiol 67:809–817.

Rockel AJ, Hiorns RW, Powell TP (1980) The basic uniformity in structure of the neocortex. Brain 103:221–244.

Rodríguez-Trelles F, Tarrío R, Ayala FJ (2004) Molecular clocks: Whence and whither? In Telling the Evolutionary Time: Molecular Clocks and the Fossil Record, eds Donoghue PCJ, Smith MP (CRC Press, Boca Raton, FL), pp 5–26.

Roe AW (2004) Modular complexity of area V2 in the macaque monkey. In The Primate Visual System, eds Kaas JH, Collins CE (CRC Press, Boca Raton, FL), pp 109–138.

Roffman RC, Norris BJ, Calabrese RL (2011) Animal-to-animal variability of connection strength in the leech heartbeat central pattern generator. J Neurophysiol 107:1681–1693.

Rogulja-Ortmann A, Technau GM (2008) Multiple roles for Hox genes in segment-specific shaping of CNS lineages. Fly (Austin) 2:316–319.

Rogulja-Ortmann A, Lüer K, Seibert J, Rickert C, Technau GM (2007) Programmed cell death in the embryonic central nervous system of Drosophila melanogaster. Development 134:105–116.

Rogulja-Ortmann A, Renner S, Technau GM (2008) Antagonistic roles for Ultrabithorax and Antennapedia in regulating segment-specific apoptosis of differentiated moto-neurons in the Drosophila embryonic central nervous system. Development 135:3435–3445.

Rokas A, Krüger D, Carroll SB (2005) Animal evolution and the molecular signature of radiations compressed in time. Science 310:1933–1938.

Rolls ET (2000) Functions of the primate temporal lobe cortical visual areas in invariant visual object and face recognition. Neuron 27:205–218.

Rolls ET, Critchley HD, Browning AS, Inoue K (2006) Face-selective and auditory neurons in the primate orbitofrontal cortex. Exp Brain Res 170:74–87.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Romanski LM (2007) Representation and integration of auditory and visual stimuli in the primate ventral lateral prefrontal cortex. Cereb Cortex 17(Suppl 1):i61–i69.

Romanski LM, Averbeck BB (2009) The primate cortical auditory system and neural representation of conspecific vocalizations. Annu Rev Neurosci 32:315–346.

Romanski LM, Diehl MM (2011) Neurons responsive to face-view in the primate ventrolateral prefrontal cortex. Neuroscience 189:223–235.

Romanski LM, Goldman-Rakic PS (2002) An auditory domain in primate prefrontal cortex. Nat Neurosci 5:15–16.

Romanski LM, Bates JF, Goldman-Rakic PS (1999a) Auditory belt and parabelt projections to the prefrontal cortex in the rhesus monkey. J Comp Neurol 403:141–157.

Romanski LM, Tian B, Fritz J, Mishkin M, Goldman-Rakic PS, Rauschecker JP (1999b) Dual streams of auditory afferents target multiple domains in the primate prefrontal cortex. Nat Neurosci 2:1131–1136.

Romanski LM, Averbeck BB, Diltz M (2005) Neural representation of vocalizations in the primate ventrolateral prefrontal cortex. J Neurophysiol 93:734–747.

Rosenkilde CE, Bauer RH, Fuster JM (1981) Single cell activity in ventral prefrontal cortex of behaving monkeys. Brain Res 209:375–394.

Rossier J, Schenk F (2003) Olfactory and/or visual cues for spatial navigation through ontogeny: Olfactory cues enable the use of visual cues. Behav Neurosci 117:412–425.

Rosvall KA, Bergeon Burns CM, Barske J, Goodson JL, Schlinger BA, Sengelaub DR, Ketterso ED (2012) Neural sensitivity to testosterone predicts individual differences in male and female aggression: Implications for behavioural evolution. Proc Roy Soc B Biol Sci, doi:10.1098/rspb.2012.0442.

Roth G, Dicke U (2005) Evolution of the brain and intelligence. Trends Cogn Sci 9:250–257.

Rothman KJ (1990) No adjustments are needed for multiple comparisons. Epidemiology 1:43–46.

Rowe TB, Macrini TE, Luo ZX (2011) Fossil evidence on origin of the mammalian brain. Science 332:955–957.

Rubow TK, Bass AH (2009) Reproductive and diurnal rhythms regulate vocal motor plasticity in a teleost fish. J Exp Biol 212:3252–3262.

Rudman WB, Darvell BW (1990) Opisthobranch molluscs of Hong Kong: Part 1. Goniodorididae, Onchidorididae, Triophidae, Gymnodorididae, Chromodorididae (Nudibranchia). Asian Marine Biology 7:31–79.

Ruiz S, Crespo P, Romo R (1995) Representation of moving tactile stimuli in the somatic sensory cortex of awake monkeys. J Neurophysiol 73:525–537.

Rusconi E, Kwan B, Giordano BL, Umiltà C, Butterworth B (2006) Spatial representation of pitch height: The SMARC effect. Cognition 99:113–129.

Russ BE, Lee YS, Cohen YE (2007) Neural and behavioral correlates of auditory categorization. Hear Res 229:204–212.

Safi K, Dechmann DK (2005) Adaptation of brain regions to habitat complexity: A comparative analysis in bats (Chiroptera). Proc Biol Sci 272:179–186.

Sakarya O, Armstrong KA, Adamska M, Adamski M, Wang IF, Tidor B, Degnan BM, Oakley TH, Kosik KS (2007) A post-synaptic scaffold at the origin of the animal kingdom. PLoS ONE 2:e506.

Sakarya O, Conaco C, Egecioglu O, Solla SA, Oakley TH, Kosik KS (2010) Evolutionary expansion and specialization of the PDZ domains. Mol Biol Evol 27:1058–1069.

Sakurai A, Newcomb JM, Lillvis JL, Katz PS (2011) Different roles for homologous interneurons in species exhibiting similar rhythmic behaviors. Curr Biol 21:1036–1043.

Salas C, Broglio C, Durán E, Gómez A, Ocaña FM, Jiménez-Moya F, Rodríguez F (2006) Neuropsychology of learning and memory in teleost fish. Zebrafish 3:157–171.

Saleem KS, Kondo H, Price JL (2008) Complementary circuits connecting the orbital and medial prefrontal networks with the temporal, insular, and opercular cortex in the macaque monkey. J Comp Neurol 506:659–693.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Sanderson MJ, Hufford L (1996) Homoplasy: The Recurrence of Similarity in Evolution (Academic Press, San Diego).

Sarko DK, Catania KC, Leitch DB, Kaas JH, Herculano-Houzel S (2009) Cellular scaling rules of insectivore brains. Front Neuroanat 3:8.

Sarnat HB, Netsky MG (1981) Evolution of the Nervous System (Oxford Univ Press, Oxford, UK), 2nd Ed.

Satterlie RA, Norekian TP (1995) Serotonergic modulation of swimming speed in the pteropod mollusc Clione limacina. III. Cerebral neurons. J Exp Biol 198:917–930.

Saxe R (2006) Uniquely human social cognition. Curr Opin Neurobiol 16:235–239.

Scarf D, Hayne H, Colombo M (2011) Pigeons on par with primates in numerical competence. Science 334:1664.

Scharff C, Haesler S (2005) An evolutionary perspective on FoxP2: Strictly for the birds? Curr Opin Neurobiol 15:694–703.

Scharff C, Petri J (2011) Evo-devo, deep homology and FoxP2: Implications for the evolution of speech and language. Philos Trans R Soc Lond B Biol Sci 366:2124–2140.

Scherf KS, Behrmann M, Humphreys K, Luna B (2007) Visual category-selectivity for faces, places and objects emerges along different developmental trajectories. Dev Sci 10:F15–F30.

Schierwater B, Eitel M, Jakob W, Osigus HJ, Hadrys H, Dellaporta SL, Kolokotronis SO, Desalle R (2009) Concatenated analysis sheds light on early metazoan evolution and fuels a modern “urmetazoon” hypothesis. PLoS Biol 7:e20.

Schlaggar BL, Brown TT, Lugar HM, Visscher KM, Miezin FM, Petersen SE (2002) Functional neuroanatomical differences between adults and school-age children in the processing of single words. Science 296:1476–1479.

Schlichting CD, Pigliucci M (1998) Phenotypic Evolution: A Reaction Norm Perspective (Sinauer, Sunderland, MA).

Schlief T, Schönherr R, Imoto K, Heinemann SH (1996) Pore properties of rat brain II sodium channels mutated in the selectivity filter domain. Eur Biophys J 25:75–91.

Schmidt H, Rickert C, Bossing T, Vef O, Urban J, Technau GM. (1997) The embryonic central nervous system lineages of Drosophila melanogaster. II. Neuroblast lineages derived from the dorsal part of the neuroectoderm. Dev Biol 189:186–204.

Schmidt MF, McLean J, Goller F (2012) Breathing and vocal control: The respiratory system as both a driver and a target of telencephalic vocal motor circuits in song birds. Exp Physiol 97:455–461.

Schmidt RS (1992) Neural correlates of frog calling: Production by two semi-independent generators. Behav Brain Res 50:17–30.

Schmidt-Hieber C, Bischofberger J (2010) Fast sodium channel gating supports localized and efficient axonal action potential initiation. J Neurosci 30:10233–10242.

Schmidt-Nielsen K (1984) Scaling: Why Is Animal Size So Important? (Cambridge Univ Press, Cambridge, UK).

Schnupp JW, Carr CE (2009) On hearing with more than one ear: Lessons from evolution. Nat Neurosci 12:692–697.

Schoenemann PT, Sheehan MJ, Glotzer LD (2005) Prefrontal white matter volume is disproportionately larger in humans than in other primates. Nat Neurosci 8:242–252.

Schoenherr CJ, Anderson DJ (1995) The neuron-restrictive silencer factor (NRSF): A coordinate repressor of multiple neuron-specific genes. Science 267:1360–1363.

Scholtz G, Dohle W (1996) Cell lineage and cell fate in crustacean embryos—a comparative approach. Int J Dev Biol 40:211–220.

Schön C, Wochnik A, Rössner A, Donow C, Knöchel W (2006) The FoxP subclass in Xenopus laevis development. Dev Genes Evol 216:641–646.

Schuhmacher H (1973) Notes on occurrence, feeding and swimming behaviour of Notarchus indicus and Melibe bucephala at Elat, Red Sea (Mollusca: Opisthobranchia). Israel J Zool 22:13–25.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Schüz A, Demianenko GP (1995) Constancy and variability in cortical structure. A study on synapses and dendritic spines in hedgehog and monkey. J Hirnforsch 36:113–122.

Schüz A, Palm G (1989) Density of neurons and synapses in the cerebral cortex of the mouse. J Comp Neurol 286:442–455.

Schweigreiter R, Roots BI, Bandtlow CE, Gould RM (2006) Understanding myelination through its evolution. Int Rev Neurobiol 73:219–273.

Scotland RW (2010) Deep homology: A view from systematics. Bioessays 32:438–449.

Scotland RW (2011) What is parallelism? Evol Dev 13:214–227.

Sears KE, Behringer RR, Rasweiler JJ, 4th, Niswander LA (2006) Development of bat flight: Morphologic and molecular evolution of bat wing digits. Proc Natl Acad Sci USA 103:6581–6586.

Seelke AM, Padberg JJ, Disbrow E, Purnell SM, Recanzone G, Krubitzer L (2011) Topographic maps within Brodmann’s area 5 of macaque monkeys. Cereb Cortex 22:1834–1850.

Seilacher A (1989) Vendozoa: Organismic construction in the Proterozoic biosphere. Lethaia 22:229–239.

Seilacher A (1999) Biomat-related lifestyles in the Precambrian. Palaios 14:86–93.

Semendeferi K, Armstrong E, Schleicher A, Zilles K, Van Hoesen GW (2001) Prefrontal cortex in humans and apes: A comparative study of area 10. Am J Phys Anthropol 114:224–241.

Sengupta B, Stemmler M, Laughlin SB, Niven JE (2010) Action potential energy efficiency varies among neuron types in vertebrates and invertebrates. PLOS Comput Biol 6:e1000840.

Shah R, Medina-Martinez O, Chu L-F, Samaco RC, Jamrich M (2006) Expression of FoxP2 during zebrafish development and in the adult brain. Int J Dev Biol 50:435–438.

Shambes GM, Gibson JM, Welker W (1978) Fractured somatotopy in granule cell tactile areas of rat cerebellar hemispheres revealed by micromapping. Brain Behav Evol 15:94–140.

Shannon P, Markiel A, Ozier O, Baliga NS, Wang JT, Ramage D, Amin N, Schwikowski B, Ideker T (2003) Cytoscape: A software environment for integrated models of biomolecular interaction networks. Genome Res 13:2498–2504.

Shea BT (1983) Size and diet in the evolution of African ape craniodental form. Folia Primatol 40:32–68.

Sherwood CC, Subiaul F, Zawidzki TW (2008) A natural history of the human mind: Tracing evolutionary changes in brain and cognition. J Anat 212:426–454.

Shi Y, Kirwan P, Smith J, Robinson HPC, Livesey FJ (2012) Human cerebral cortex development from pluripotent stem cells to functional excitatory synapses. Nat Neurosci 15:477–486, S1.

Shibanai S (1988) Ultrastructure of the Eimer’s organs of the Japanese shrew mole, Urotrichus talpoides (Insectivora, Mammalia) and their changes following infraorbital axotomy. Anat Anz 165:105–129.

Shu D (2003) A paleontological perspective of vertebrate origin. Chin Sci Bull 48:725–735.

Shu D-G, Conway Morris S, Zhang X-L (1996a) A Pikaia-like chordate from the Lower Cambrian of China. Nature 384:157–158.

Shu D-G, Zhang X, Chen L (1996b) Reinterpretation of Yunnanozoon as the earliest known hemichordate. Nature 380:428–430.

Shu D-G, Luo H-L, Conway Morris S, Zhang X-L, Hu S-X, Chen L, Han J, Zhu M, Li Y, Chen L-Z (1999) Lower Cambrian vertebrates from south China. Nature 402:42–46.

Shu D-G, Chen L, Han J, Zhang X-L (2001) An Early Cambrian tunicate from China. Nature 411:472–473.

Shu D-G, Conway Morris S, Han J, Zhang ZF, Yasui K, Janvier P, Chen L, Zhang XL, Liu JN, Li Y, Liu HQ (2003) Head and backbone of the Early Cambrian vertebrate Haikouichthys. Nature 421:526–529.

Shu D-G, Conway Morris S, Zhang Z-F, Han J (2010) The earliest history of the deuterostomes: The importance of the Chengjiang Fossil-Lagerstatte. Proc Biol Sci 277:165–174.

Shubin N, Tabin C, Carroll S (2009) Deep homology and the origins of evolutionary novelty. Nature 457:818–823.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Siegenthaler JA, Ashique AM, Zarbalis K, Patterson KP, Hecht JH, Kane MA, Folias AE, Choe Y, May SR, Kume T, Napoli JL, Peterson AS, Pleasure SJ (2009) Retinoic acid from the meninges regulates cortical neuron generation. Cell 139:597–609.

Sikela JM (2006) The jewels of our genome: The search for the genomic changes underlying the evolutionarily unique capacities of the human brain. PLoS Genet 2:e80.

Sliwa J, Duhamel JR, Pascalis O, Wirth S (2011) Spontaneous voice-face identity matching by rhesus monkeys for familiar conspecifics and humans. Proc Natl Acad Sci USA 108:1735–1740.

Smale L, Heideman PD, French JA (2005) Behavioral neuroendocrinology in non--traditional species of mammals: Things the “knockout” mouse CAN’T tell us. Horm Behav 48:474–483.

Smith ESJ, Omerbaši´c D, Lechner SG, Anirudhan G, Lapatsina L, Lewin GR (2011) The molecular basis of acid insensitivity in the African naked mole-rat. Science 334:1557–1560.

Smith LB, Sera MD (1992) A developmental analysis of the polar structure of dimensions. Cognit Psychol 24:99–142.

Smith TL, Povel DE, Kardong KV (2002) Predatory strike of the tentacled snake (Erpeton tentaculatum). J Zool 256:233–242.

Sneath PHA, Sokal RR (1973) Numerical Taxonomy (Freeman, San Francisco).

Snel B, Lehmann G, Bork P, Huynen MA (2000) STRING: A Web-server to retrieve and display the repeatedly occurring neighbourhood of a gene. Nucleic Acids Res 28:3442–3444.

Sokal RR, Sneath PHA (1963) Principles of Numerical Taxonomy (Freeman, San Francisco).

Soma KK (2006) Testosterone and aggression: Berthold, birds and beyond. J Neuroendocrinol 18:543–551.

Somel M, Franz H, Yan Z, Lorenc A, Guo S, Giger T, Kelso J, Nickel B, Dannemann M, Bahn S, Webster MJ, Weickert CS, Lachmann M, Pääbo S, Khaitovich P (2009) Transcriptional neoteny in the human brain. Proc Natl Acad Sci USA 106:5743–5748.

Somel M, Guo S, Fu N, Yan Z, Hu HY, Xu Y, Yuan Y, Ning Z, Hu Y, Menzel C, Hu H, Lachmann M, Zeng R, Chen W, Khaitovich P (2010) MicroRNA, mRNA, and protein expression link development and aging in human and macaque brain. Genome Res 20:1207–1218.

Sosulski DL, Bloom ML, Cutforth T, Axel R, Datta SR (2011) Distinct representations of olfactory information in different cortical centres. Nature 472:213–216.

Spector F, Maurer D (2009) Synesthesia: A new approach to understanding the development of perception. Dev Psychol 45:175–189.

Spirin V, Mirny LA (2003) Protein complexes and functional modules in molecular networks. Proc Natl Acad Sci USA 100:12123–12128.

Spiteri E, Konopka G, Coppola G, Bomar J, Oldham M, Ou J, Vernes SC, Fisher SE, Ren B, Geschwind DH (2007) Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. Am J Hum Genet 81:1144–1157.

Sporns O, Kötter R (2004) Motifs in brain networks. PLoS Biol 2:e369.

Sporns O, Zwi JD (2004) The small world of the cerebral cortex. Neuroinformatics 2(2): 145–162.

Srinivasan M, Carey S (2010) The long and the short of it: On the nature and origin of functional overlap between representations of space and time. Cognition 116:217–241.

Srivastava M, Simakov O, Chapman J, Fahey B, Gauthier ME, Mitros T, Richards GS, Conaco C, Dacre M, Hellsten U, Larroux C, Putnam NH, Stanke M, Adamska M, Darling A, Degnan SM, Oakley TH, Plachetzki DC, Zhai Y, Adamski M, Calcino A, Cummins SF, Goodstein DM, Harris C, Jackson DJ, Leys SP, Shu S, Woodcroft BJ, Vervoort M, Kosik KS, Manning G, Degnan BM, Rokhsar DS (2010) The Amphimedon queenslandica genome and the evolution of animal complexity. Nature 466:720–726.

Stanovich KE (2004) The Robot’s Rebellion: Finding Meaning in the Age of Darwin (Univ of Chicago Press, Chicago).

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Stein BE, Meredith MA (1993) The Merging of the Senses (MIT Press, Cambridge, MA).

Stein BE, Stanford TR (2008) Multisensory integration: Current issues from the perspective of the single neuron. Nat Rev Neurosci 9:255–266.

Steinberg JE (1956) The pelagic nudibranch, Cephalopyge trematoides (Chun, 1889), in New South Wales with a note on other species in this genus. Proc Linn Soc NSW 81:184–192.

Steinman MQ, Knight JA, Trainor BC (2012) Effects of photoperiod and food restriction on the reproductive physiology of female California mice. Gen Comp Endocrinol 176: 391–399.

Stephan H, Frahm H, Baron G (1981) New and revised data on volumes of brain structures in insectivores and primates. Folia Primatol (Basel) 35:1–29.

Stephens DW (1991) Change, regularity, and value in the evolution of animal learning. Behav Ecol 2:77–89.

Stephens DW, Krebs JR (1986) Foraging Theory (Princeton Univ Press, Princeton, NJ).

Stepniewska I, Kaas JH (1996) Topographic patterns of V2 cortical connections in macaque monkeys. J Comp Neurol 371:129–152.

Stepniewska I, Fang PC, Kaas JH (2005) Microstimulation reveals specialized subregions for different complex movements in posterior parietal cortex of prosimian galagos. Proc Natl Acad Sci USA 102:4878–4883.

Stepniewska I, Friedman RM, Gharbawie OA, Cerkevich CM, Roe AW, Kaas JH (2011) Optical imaging in galagos reveals parietal-frontal circuits underlying motor behavior. Proc Natl Acad Sci USA 108:E725–E732.

Sterbing-D’Angelo S, Chadha M, Chiu C, Falk B, Xian W, Barcelo J, Zook JM, Moss CF (2011) Bat wing sensors support flight control. Proc Natl Acad Sci USA 108:11291–11296.

Stern M, Kreber R, Ganetzky B (1990) Dosage effects of a Drosophila sodium channel gene on behavior and axonal excitability. Genetics 124:133–143.

Stevens CF (1989) How cortical interconnectedness varies with network size. Neural Comput 1(4):473–479.

Stollewerk A, Chipman AD (2006) Neurogenesis in myriapods and chelicerates and its importance for understanding arthropod relationships. Integr Comp Biol 46:195–206.

Stollewerk A, Weller M, Tautz D (2001) Neurogenesis in the spider Cupiennius salei. Development 128:2673–2688.

Straka H, Baker R, Gilland E (2006) Preservation of segmental hindbrain organization in adult frogs. J Comp Neurol 494:228–245.

Strassman JE, Queller DC, Avise JC, AyalaFJ, eds (2011) In the Light of Evolution Volume V: Cooperation and Conflict (National Academies Press, Washington, DC).

Strausfeld NJ (2012) Arthropod Brains: Evolution, Functional Elegance, and Historical Significance (Harvard Univ Press, Cambridge, MA).

Strausfeld NJ, Sinakevitch I, Brown SM, Farris SM (2009) Ground plan of the insect mushroom body: Functional and evolutionary implications. J Comp Neurol 513:265–291.

Striedter GF (1997) The telencephalon of tetrapods in evolution. Brain Behav Evol 49: 179–213.

Striedter GF (1998) Stepping into the same river twice: Homologues as recurring attractors in epigenetic landscapes. Brain Behav Evol 52:218–231.

Striedter GF (2005) Principles of Brain Evolution (Sinauer, Sunderland, MA).

Striedter GF, Charvet CJ (2008) Developmental origins of species differences in telencephalon and tectum size: Morphometric comparisons between a parakeet (Melopsittacus undulatus) and a quail (Colinus virgianus). J Comp Neurol 507:1663–1675.

Striedter GF, Northcutt RG (1991) Biological hierarchies and the concept of homology. Brain Behav Evol 38:177–189.

Stromswold K, Caplan D, Alpert N, Rauch S (1996) Localization of syntactic comprehension by positron emission tomography. Brain Lang 52:452–473.

Strong M, Chandy KG, Gutman GA (1993) Molecular evolution of voltage-sensitive ion channel genes: On the origins of electrical excitability. Mol Biol Evol 10:221–242.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Stuart AE, Hunter FF, Currie DC (2002) Using behavioural characters in phylogeny reconstruction. Ethol Ecol Evol 14:129–139.

Stuart JM, Segal E, Koller D, Kim SK (2003) A gene-coexpression network for global discovery of conserved genetic modules. Science 302:249–255.

Subiaul F, Barth J, Okamoto-Barth S, Povinelli DJ (2007) Human cognitive specializations. In Evolution of Nervous Systems: Primates, eds Kaas JH, Preuss TM (Elsevier, Amsterdam), Vol 4, pp 509–528.

Suga N, Simmons JA, Jen PH (1975) Peripheral specialization for fine analysis of doppler-shifted echoes in the auditory system of the “CF-FM” bat Pteronotus parnellii. J Exp Biol 63:161–192.

Suga N, Niwa H, Taniguchi I, Margoliash D (1987) The personalized auditory cortex of the mustached bat: Adaptation for echolocation. J Neurophysiol 58:643–654.

Sugase Y, Yamane S, Ueno S, Kawano K (1999) Global and fine information coded by single neurons in the temporal visual cortex. Nature 400:869–873.

Sugihara T, Diltz MD, Averbeck BB, Romanski LM (2006) Integration of auditory and visual communication information in the primate ventrolateral prefrontal cortex. J Neurosci 26:11138–11147.

Sugita Y (2008) Face perception in monkeys reared with no exposure to faces. Proc Natl Acad Sci USA 105:394–398.

Sur M, Leamey CA (2001) Development and plasticity of cortical areas and networks. Nat Rev Neurosci 2:251–262.

Sur M, Rubenstein JL (2005) Patterning and plasticity of the cerebral cortex. Science 310: 805–810.

Sur M, Wall JT, Kaas JH (1981) Modular segregation of functional cell classes within the postcentral somatosensory cortex of monkeys. Science 212:1059–1061.

Sur M, Wall JT, Kaas JH (1984) Modular distribution of neurons with slowly adapting and rapidly adapting responses in Area 3b of somatosensory cortex in monkeys. J Neurophysiol 51:724–744.

Suzuki H, Azuma M (1983) Topographic studies on visual neurons in the dorsolateral prefrontal cortex of the monkey. Exp Brain Res 53:47–58.

Taghert PH, Willows AOD (1978) Control of a fixed action pattern by single, central neurons in the marine mollusk, Tritonia diomedea. J Comp Physiol 123:253–259.

Takahashi K, Liu F-C, Hirokawa K, Takahashi H (2003) Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum. J Neurosci Res 73:61–72.

Takahashi K, Liu FC, Oishi T, Mori T, Higo N, Hayashi M, Hirokawa K, Takahashi H (2008) Expression of FOXP2 in the developing monkey forebrain: Comparison with the expression of the genes FOXP1, PBX3, and MEIS2. J Comp Neurol 509:180–189.

Takahata T, Higo N, Kaas JH, Yamamori T (2009a) Expression of immediate-early genes reveals functional compartments within ocular dominance columns after brief monocular inactivation. Proc Natl Acad Sci USA 106:12151–12155.

Takahata T, Komatsu Y, Watakabe A, Hashikawa T, Tochitani S, Yamamori T (2009b) Differential expression patterns of occ1-related genes in adult monkey visual cortex. Cereb Cortex 19:1937–1951.

Takahata T, Shukla R, Yamamori T, Kaas JH (2011) Differential expression patterns of striate cortex enriched genes among Old World, New World, and prosimian primates. Cereb Cortex, doi:10.1093/cercor/bhr308.

Tallafuss A, Bally-Cuif L (2002) Formation of the head-trunk boundary in the animal body plan: An evolutionary perspective. Gene 287:23–32.

Tanigawa H, Lu HD, Roe AW (2010) Functional organization for color and orientation in macaque V4. Nat Neurosci 13:1542–1548.

Tanila H, Carlson S, Linnankoski I, Kahila H (1993) Regional distribution of functions in dorsolateral prefrontal cortex of the monkey. Behav Brain Res 53:63–71.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Tardy J, Gantes H (1980) Un Mollusque Nudibranche peu connu: Cumanotus cuenoti A. Pruvot-Fol (1948); redescription, biologie. Bull Soc Zool Fr 105:199–207.

Taylor MF, Heckel DG, Brown TM, Kreitman ME, Black B (1993) Linkage of pyrethroid insecticide resistance to a sodium channel locus in the tobacco budworm. Insect Biochem Mol Biol 23:763–775.

Technau GM, Berger C, Urbach R (2006) Generation of cell diversity and segmental pattern in the embryonic central nervous system of Drosophila. Dev Dyn 235:861–869.

Tennant KA, Adkins DL, Donlan NA, Asay AL, Thomas N, Kleim JA, Jones TA (2011) The organization of the forelimb representation of the C57BL/6 mouse motor cortex as defined by intracortical microstimulation and cytoarchitecture. Cereb Cortex 21:865–876.

Teramitsu I, Kudo LC, London SE, Geschwind DH, White SA (2004) Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction. J Neurosci 24:3152–3163.

Terrace HS, Petitto LA, Sanders RJ, Bever TG (1979) Can an ape create a sentence? Science 206:891–902.

Thewissen JGM, Nummela S (2008) Sensory Evolution on the Threshold: Adaptations in Secondarily Aquatic Vertebrates (Univ of California Press, Berkeley).

Thollesson M (1999) Phylogenetic analysis of dorid nudibranchs (Gastropoda: Doridacea) using the mitochondrial 16S rRNA gene. J Molluscan Stud 65:335–353.

Thompson S, Watson WH, 3rd (2005) Central pattern generator for swimming in Melibe. J Exp Biol 208:1347–1361.

Thompson TE (1980) Jamaican opisthobranch molluscs II. J Mollusc Stud 46:74-99.

Thompson TE, Brown GH (1981) Biology and relationships of the nudibranch mollusc Notobryon wardi in South Africa, with a review of the Scyllaeidae. J Zool (Lond) 194:437–444.

Thompson TE, Brown GH (1984) Biology of the Opisthobranch Molluscs (Ray Society, London), Vol 2.

Thompson TE, Crampton DM (1984) Biology of Melibe fimbriata, a conspicuous opisthobranch mollusc of the Indian Ocean, which has now invaded the Mediterranean Sea. J Mollusc Stud 50:113–121.

Thompson TE, Slinn DJ (1959) On the biology of the opisthobranch Pleurobranchus membranaceus. J Mar Biol Assoc U K 38:507–524.

Thomson KS (1968) Lung ventilation in dipnoan fishes. Postila 122:1–6.

Thorpe SJ, Rolls ET, Maddison S (1983) The orbitofrontal cortex: Neuronal activity in the behaving monkey. Exp Brain Res 49:93–115.

Tian B, Reser D, Durham A, Kustov A, Rauschecker JP (2001) Functional specialization in rhesus monkey auditory cortex. Science 292:290–293.

Tian LM, Kawai R, Crow T (2006) Serotonin-immunoreactive CPT interneurons in Hermissenda: Identification of sensory input and motor projections. J Neurophysiol 96:327–335.

Tomasello M, Call J (1997) Primate Cognition (Oxford Univ Press, New York).

Tomer R, Denes AS, Tessmar-Raible K, Arendt D (2010) Profiling by image registration reveals common origin of annelid mushroom bodies and vertebrate pallium. Cell 142:800–809.

Tooby J, Cosmides L (1992) The psychological foundations of culture. In The Adapted Mind: Evolutionary Psychology and the Generation of Culture, eds Barkow J, Cosmides C, Tooby J (Oxford Univ Press, New York), pp 19–136.

Tower DB (1954) Structural and functional organization of mammalian cerebral cortex: The correlation of neurone density with brain size. Cortical neurone density in the fin whale (Balaenoptera physalus L.) with a note on the cortical neurone density in the Indian elephant. J Comp Neurol 101:19–51.

Zeiss Atlas 995 Manual Dexterity Test

Traag VA, Bruggeman J (2009) Community detection in networks with positive and negative links. Phys Rev E Stat Nonlin Soft Matter Phys 80:036115.

Tracy HC (1959) Stages in the development of the anatomy of motility of the toadfish (Opsanus tau). J Comp Neurol 111:27–81.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Tracy HC (1961) Development of the spinal neural crest, nerves, and muscles in the toadfish (Opsanus tau). J Comp Neurol 116:291–315.

Tsao DY, Freiwald WA, Knutsen TA, Mandeville JB, Tootell RB (2003) Faces and objects in macaque cerebral cortex. Nat Neurosci 6:989–995.

Tsao DY, Moeller S, Freiwald WA (2008a) Comparing face patch systems in macaques and humans. Proc Natl Acad Sci USA 105:19514–19519.

Tsao DY, Schweers N, Moeller S, Freiwald WA (2008b) Patches of face-selective cortex in the macaque frontal lobe. Nat Neurosci 11:877–879.

Tsoar A, Nathan R, Bartan Y, Vyssotski A, Dell’Omo G, Ulanovsky N (2011) Large-scale navigational map in a mammal. Proc Natl Acad Sci USA 108:E718–E724.

Tudusciuc O, Nieder A (2007) Neuronal population coding of continuous and discrete quantity in the primate posterior parietal cortex. Proc Natl Acad Sci USA 104:14513–14518.

Tümpel S, Wiedemann LM, Krumlauf R (2009) Hox genes and segmentation of the vertebrate hindbrain. In HOX Genes, ed Pourquié O (Academic, New York), Vol 88, pp 103–137.

Uddin M, Wildman DE, Liu G, Xu W, Johnson RM, Hof PR, Kapatos G, Grossman LI, Goodman M (2004) Sister grouping of chimpanzees and humans as revealed by genome-wide phylogenetic analysis of brain gene expression profiles. Proc Natl Acad Sci USA 101:2957–2962.

Udny Yule G (1925) A mathematical theory of evolution, based on the conclusions of Dr. JC Willis, FRS. R Soc Lond Philos Trans B 213:21–87.

Udolph G, Prokop A, Bossing T, Technau GM (1993) A common precursor for glia and neurons in the embryonic CNS of Drosophila gives rise to segment-specific lineage variants. Development 118:765–775.

Uhlhaas PJ, Singer W (2010) Abnormal neural oscillations and synchrony in schizophrenia. Nat Rev Neurosci 11:100–113.

Ulanovsky N, Moss CF (2007) Hippocampal cellular and network activity in freely moving echolocating bats. Nat Neurosci 10:224–233.

Ungerleider LG, Mishkin M (1982) Two cortical visual systems. In Analysis of Visual Behavior, eds Ingle DJ, Goodale MA, Mansfield RJW (MIT Press, Cambridge, MA), pp 549–586.

Ungerleider LG, Gaffan D, Pelak VS (1989) Projections from inferior temporal cortex to prefrontal cortex via the uncinate fascicle in rhesus monkeys. Exp Brain Res 76:473–484.

Urbano FJ, Simpson JI, Llinás RR (2006) Somatomotor and oculomotor inferior olivary neurons have distinct electrophysiological phenotypes. Proc Natl Acad Sci USA 103: 16550–16555.

Uttal WR (2001) The New Phrenology: The Limits of Localizing Cognitive Processes in the Brain (MIT Press, Cambridge, MA).

Vaccarino FM, Schwartz ML, Raballo R, Nilsen J, Rhee J, Zhou M, Doetschman T, Coffin JD, Wyland JJ, Hung YT (1999) Changes in cerebral cortex size are governed by fibroblast growth factor during embryogenesis. Nat Neurosci 2:246–253.

Valdes A (2003) A phylogenetic analysis and systematic revision of the cryptobranch dorids (Mollusca, Nudibranchia, Anthobranchia). Zool J Linn Soc Lond 136:535–636.

Valero J, Weruaga E, Murias AR, Recio JS, Alonso JR (2005) Proliferation markers in the adult rodent brain: Bromodeoxyuridine and proliferating cell nuclear antigen. Brain Res Brain Res Protoc 15:127–134.

Vallbo AB, Johansson RS (1984) Properties of cutaneous mechanoreceptors in the human hand related to touch sensation. Hum Neurobiol 3:3–14.

Van Der Loos H (1976) Barreloids in mouse somatosensory thalamus. Neurosci Lett 2:1–6.

Van Essen DC (1997) A tension-based theory of morphogenesis and compact wiring in the central nervous system. Nature 385:313–318.

Van Essen DC, Newsome WT, Maunsell JH, Bixby JL (1986) The projections from striate cortex (V1) to areas V2 and V3 in the macaque monkey: Asymmetries, areal boundaries, and patchy connections. J Comp Neurol 244:451–480.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

van Noort V, Snel B, Huynen MA (2003) Predicting gene function by conserved coexpression. Trends Genet 19:238–242.

van Rijzingen IM, Gispen WH, Spruijt BM (1995) Olfactory bulbectomy temporarily impairs Morris maze performance: An ACTH(4-9) analog accellerates return of function. Physiol Behav 58:147–152.

Van Vleck DB (1965) The anatomy of the nasal rays of Condylura cristata. J Mammal 46:248–253.

Van Vreeswijk C, Abbott LF, Ermentrout GB (1994) When inhibition not excitation synchronizes neural firing. J Comput Neurosci 1:313–321.

vanMarle K, Wynn K (2006) Six-month-old infants use analog magnitudes to represent duration. Dev Sci 9:F41–F49.

Vargha-Khadem F, Passingham RE (1990) Speech and language defects. Nature 346:226–226.

Vargha-Khadem F, Watkins K, Alcock K, Fletcher P, Passingham R (1995) Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder. Proc Natl Acad Sci USA 92:930–933.

Vargha-Khadem F, Watkins KE, Price CJ, Ashburner J, Alcock KJ, Connelly A, Frackowiak RS, Friston KJ, Pembrey ME, Mishkin M, Gadian DG, Passingham RE (1998) Neural basis of an inherited speech and language disorder. Proc Natl Acad Sci USA 95:12695–12700.

Vargha-Khadem F, Gadian DG, Copp A, Mishkin M (2005) FOXP2 and the neuroanatomy of speech and language. Nat Rev Neurosci 6:131–138.

Varki A, Nelson DL (2007) Genomic comparisons of humans and chimpanzees. Annu Rev Anthropol 36:191–209.

Varki A, Geschwind DH, Eichler EE (2008) Explaining human uniqueness: Genome interactions with environment, behaviour and culture. Nat Rev Genet 9:749–763.

Venkatesh B, Lu SQ, Dandona N, See SL, Brenner S, Soong TW (2005) Genetic basis of tetrodotoxin resistance in pufferfishes. Curr Biol 15:2069–2072.

Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, Geschwind DH, Fisher SE (2007) High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. Am J Hum Genet 81:1232–1250.

Vernes SC, Oliver PL, Spiteri E, Lockstone HE, Puliyadi R, Taylor JM, Ho J, Mombereau C, Brewer A, Lowy E, Nicod J, Groszer M, Baban D, Sahgal N, Cazier JB, Ragoussis J, Davies KE, Geschwind DH, Fisher SE. (2011) Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genet 7:e1002145.

Vescovi AL, Reynolds BA, Fraser DD, Weiss S (1993) bFGF regulates the proliferative fate of unipotent (neuronal) and bipotent (neuronal/astroglial) EGF-generated CNS progenitor cells. Neuron 11:951–966.

Vieyra M (2011) Olfactory receptor genes in terrestrial, freshwater, and sea turtles: Evidence for a reduction in the number of functional genes in aquatic species. Chelonian Conserv Biol 10:181–187.

Vincente N (1963) Une des plus belles espèces de nudibranchs, Hexabranchus marginatus. Rec Trav Stat Mar End Bull 28:99–106.

Voges D, Zwickl P, Baumeister W (1999) The 26S proteasome: A molecular machine designed for controlled proteolysis. Annu Rev Biochem 68:1015–1068.

Volet SD, Clement A, Fayol M (2008) Time, number and length: Similarities and differences in discrimination in adults and children. Q J Exp Psychol 61:1827–1846.

von Bonin G (1937) Brain weight and body weight in mammals. J Gen Psychol 16: 379–389.

von Salvini-Plawen L, Mayr M (1977) On the evolution of photoreceptors and eyes. Evol Biol 10:207–263.

Vonnemann V, Schrodl M, Klussmann-Kolb A, Wagele H (2005) Reconstruction of the phylogeny of the Opisthobranchia (Mollusca: Gastropoda) by means of 18S and 28S rRNA gene sequences. J Molluscan Stud 71:113–125.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Wacker DW, Schlinger BA, Wingfield JC (2008) Combined effects of DHEA and fadrozole on aggression and neural VIP immunoreactivity in the non-breeding male song sparrow. Horm Behav 53:287–294.

Waddington CH (1957) The Strategy of the Genes. A Discussion of Some Aspects of Theoretical Biology (Macmillan, New York).

Waegele H, Willan RC (2000) Phylogeny of the Nudibranchia. Zool J Linn Soc 130:83–181.

Waggoner B (2003) The Ediacaran biotas in space and time. Integr Comp Biol 43: 104–113.

Wagner GP (2007) The developmental genetics of homology. Nat Rev Genet 8: 473–479.

Wahba GM, Hostikka SL, Carpenter EM (2001) The paralogous Hox genes Hoxa10 and Hoxd10 interact to pattern the mouse hindlimb peripheral nervous system and skeleton. Dev Biol 231:87–102.

Wake DB, Wake MH, Specht CD (2011) Homoplasy: From detecting pattern to determining process and mechanism of evolution. Science 331:1032–1035.

Walker P, Bremner JG, Mason U, Spring J, Mattock K, Slater A, Johnson SP (2010) Preverbal infants’ sensitivity to synaesthetic cross-modality correspondences. Psychol Sci 21:21–25.

Wallace DG, Gorny B, Whishaw IQ (2002) Rats can track odors, other rats, and themselves: Implications for the study of spatial behavior. Behav Brain Res 131:185–192.

Wallman J (1992) Aping Language (Cambridge Univ Press, Cambridge, UK).

Wallraff HG (2004) Avian olfactory navigation: Its empirical foundation and conceptual state. Anim Behav 67:189–204.

Wallraff HG (2005) Avian Navigation: Pigeon Homing as a Paradigm (Springer-Verlag, Berlin).

Walsh V (2003) A theory of magnitude: Common cortical metrics of time, space and quantity. Trends Cogn Sci 7:483–488.

Walshe J, Mason I (2000) Expression of FGFR1, FGFR2, and FGFR3 during early neural development in the chick embryo. Mech Dev 90:103–110.

Wang SSH, Shultz JR, Burish MJ, Harrison KH, Hof PR, Towns LC, Wagers MW, Wyatt KD (2008) Functional trade-offs in white matter axonal scaling. J Neurosci 28:4047–4056.

Warrington EK (1982) The fractionation of arithmetical skills: A single case study. Q J Exp Psychol A 34:31–51.

Watkins KE, Dronkers NF, Vargha-Khadem F (2002a) Behavioural analysis of an inherited speech and language disorder: Comparison with acquired aphasia. Brain 125:452–464.

Watkins KE, Vargha-Khadem F, Ashburner J, Passingham RE, Connelly A, Friston KJ, Frac-kowiak RS, Mishkin M, Gadian DG (2002b) MRI analysis of an inherited speech and language disorder: Structural brain abnormalities. Brain 125:465–478.

Watson WH, Lawrence KA, Newcomb JM (2001) Neuroethology of Melibe leonina swimming behavior. Am Zool 41:1026–1035.

Watson WH, 3rd, Newcomb JM, Thompson S (2002) Neural correlates of swimming behavior in Melibe leonina. Biol Bull 203:152–160.

Watts DJ, Strogatz SH (1998) Collective dynamics of “small-world” networks. Nature 393: 440–442.

Weatherbee SD, Behringer RR, Rasweiler JJ, 4th, Niswander LA (2006) Interdigital webbing retention in bat wings illustrates genetic changes underlying amniote limb diversification. Proc Natl Acad Sci USA 103:15103–15107.

Webster MJ, Bachevalier J, Ungerleider LG (1994) Connections of inferior temporal areas TEO and TE with parietal and frontal cortex in macaque monkeys. Cereb Cortex 4:470–483.

Weeg MS, Land BR, Bass AH (2005) Vocal pathways modulate efferent neurons to the inner ear and lateral line. J Neurosci 25:5967–5974.

Welker W (1990) Why does cerebral cortex fissure and fold? A review of determinants of gyri and sulci. In Comparative Structure and Evolution of Cerebral Cortex, eds Jones EG, Peters A (Plenum Press, New York), Vol 8B, Part II, pp 3–136.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Weller M, Tautz D (2003) Prospero and Snail expression during spider neurogenesis. Dev Genes Evol 213:554–566.

Welsh JP, Lang EJ, Sugihara I, Llinás R (1995) Dynamic organization of motor control within the olivocerebellar system. Nature 374:453–457.

Wen Q, Chklovskii DB (2005) Segregation of the brain into gray and white matter: A design minimizing conduction delays. PLOS Comput Biol 1(7):e78.

Wente SR, Rout MP (2010) The nuclear pore complex and nuclear transport. Cold Spring Harb Perspect Biol 2:a000562.

Wenzel JW (1992) Behavioral homology and phylogeny. Annu Rev Ecol Syst 23:361–381.

West GB, Brown JH (2005) The origin of allometric scaling laws in biology from genomes to ecosystems: Towards a quantitative unifying theory of biological structure and organization. J Exp Biol 208:1575–1592.

West GB, Woodruff WH, Brown JH (2002) Allometric scaling of metabolic rate from molecules and mitochondria to cells and mammals. Proc Natl Acad Sci USA 99(Suppl 1): 2473–2478.

West JW, Patton DE, Scheuer T, Wang Y, Goldin AL, Catterall WA (1992) A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation. Proc Natl Acad Sci USA 89:10910–10914.

Weston P, Wieland C (2003) The mole. Creation Magazine 25:46–50.

Wetterbom A, Sevov M, Cavelier L, Bergström TF (2006) Comparative genomic analysis of human and chimpanzee indicates a key role for indels in primate evolution. J Mol Evol 63:682–690.

Whiten A (2011) The scope of culture in chimpanzees, humans and ancestral apes. Philos Trans R Soc Lond B Biol Sci 366:997–1007.

Whiting BA, Barton RA (2003) The evolution of the cortico-cerebellar complex in primates: Anatomical connections predict patterns of correlated evolution. J Hum Evol 44:3–10.

Whiting MF, Bradler S, Maxwell T (2003) Loss and recovery of wings in stick insects. Nature 421:264–267.

Whitman CO (1899) Animal Behavior. Biological Lectures of the Marine Biological Laboratory (Woods Hole Marine Biological Laboratory, Woods Hole, MA).

Whittington HB (1985) The Burgess Shale (Yale University Press, New Haven, CT).

Widmark J, Sundström G, Ocampo Daza D, Larhammar D (2011) Differential evolution of voltage-gated sodium channels in tetrapods and teleost fishes. Mol Biol Evol 28:859–871.

Wiens JJ, Kuczynski CA, Duellman WE, Reeder TW (2007) Loss and re-evolution of complex life cycles in marsupial frogs: Does ancestral trait reconstruction mislead? Evolution 61:1886–1899.

Wiesel TN, Hubel DH, Lam DMK (1974) Autoradiographic demonstration of ocular-dominance columns in the monkey striate cortex by means of transneuronal transport. Brain Res 79:273–279.

Wikler KC, Rakic P (1990) Distribution of photoreceptor subtypes in the retina of diurnal and nocturnal primates. J Neurosci 10:3390–3401.

Wild JM, Kubke MF, Mooney R (2009) Avian nucleus retroambigualis: Cell types and projections to other respiratory-vocal nuclei in the brain of the zebra finch (Taeniopygia guttata). J Comp Neurol 512:768–783.

Wiley EO, Lieberman BS (2011) Phylogenetics (Wiley-Blackwell, Hoboken, NJ).

Willan RC, Coleman N (1984) Nudibranchs of Australia (Australasian Marine Photographic Index, Sydney).

Williams BL, Caldwell RL (2009) Intra-organismal distribution of tetrodotoxin in two species of blue-ringed octopuses (Hapalochlaena fasciata and H. lunulata). Toxicon 54:345–353.

Williams RW, Herrup K (1988) The control of neuron number. Annu Rev Neurosci 11:423–453.

Willows AO (1967) Behavioral acts elicited by stimulation of single, identifiable brain cells. Science 157:570–574.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Willows AOD, Dorsett DA (1975) Evolution of swimming behavior in Tritonia and its neurophysiological correlates. J Comp Physiol 100:117–133.

Willows AOD, Pavlova GA, Phillips NE (1997) Modulation of ciliary beat frequency by neuropeptides from identified molluscan neurons. J Exp Biol 200:1433–1439.

Wilson CH, Hartline DK (2011) Novel organization and development of copepod myelin. II. Nonglial origin. J Comp Neurol 519:3281–3305.

Wilson DA, Stevenson RJ (2006) Learning to Smell: Olfactory Perception from Neurobiology to Behavior (Johns Hopkins Univ Press, Baltimore, MD).

Wilson FA, Scalaidhe SP, Goldman-Rakic PS (1993) Dissociation of object and spatial processing domains in primate prefrontal cortex. Science 260:1955–1958.

Wilson NG (2003) Australian Aphelodoris (Mollusca: Nudibranchia): Two new species, sperm ultrastructure and a redescription of Aphelodoris greeni Burn. In The Marine Flora and Fauna of Dampier, Western Australia, eds Wells FE, Walker DI, Jones DS (Western Australian Museum, Perth), pp 563–587.

Wiltschko W, Wiltschko R (2005) Magnetic orientation and magnetoreception in birds and other animals. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 191:675–693.

Wingfield JC (2005) Historical contributions of research on birds to behavioral neuroendocrinology. Horm Behav 48:395–402.

Winters W, Kado R, Adey W (1969) A Stereotaxic Brain Atlas for Macaca nemestrina (Univ of California Press, Los Angeles).

Wise LZ, Pettigrew JD, Calford MB (1986) Somatosensory cortical representation in the Australian ghost bat, Macroderma gigas. J Comp Neurol 248:257–262.

Wollberg Z, Sela J (1980) Frontal cortex of the awake squirrel monkey: Responses of single cells to visual and auditory stimuli. Brain Res 198:216–220.

Wollscheid-Lengeling E, Boore J, Brown W, Waegele H (2001) The phylogeny of Nudibranchia (Opisthobranchia, Gastropoda, Mollusca) reconstructed by three molecular markers. Org Divers Evol 1:241–256.

Woolsey TA, Van der Loos H (1970) The structural organization of layer IV in the somatosensory region (SI) of mouse cerebral cortex. The description of a cortical field composed of discrete cytoarchitectonic units. Brain Res 17:205–242.

Woolsey TA, Welker C, Schwartz RH (1975) Comparative anatomical studies of the SmL face cortex with special reference to the occurrence of “barrels” in layer IV. J Comp Neurol 164:79–94.

Wrangham R (2009) Catching Fire: How Cooking Made Us Human (Basic Books, New York).

Wray GA, Levinton JS, Shapiro LH (1996) Molecular evidence for deep Precambrian divergences among metazoan phyla. Science 274:568–573.

Wright WG, Jones K, Sharp P, Maynard B (1995) Widespread anatomical projections of the serotonergic modulatory neuron, CB1, in Aplysia. Invert Neurosci 1:173–183.

Wu D-D, Irwin DM, Zhang Y-P (2011) De novo origin of human protein-coding genes. PLoS Genet 7:e1002379.

Wynn K (1990) Children’s understanding of counting. Cognition 36:155–193.

Wynn K (1992) Children’s acquisition of the number words and the counting system. Cognit Psychol 24:220–251.

Xian-Guang H, Aldridge RJ, Bergstrom J, Siveter DJ, Siveter DJ, Feng X-H (2004) The Cambrian Fossils of Chengjiang, China (Blackwell, Oxford).

Xiao S, Zhang Y, Knoll AH (1998) Three-dimensional preservation of algae and animal embryos in a Neoproterozoic phosphorite. Nature 391:553–558.

Xiao Y, Wang Y, Felleman DJ (2003) A spatially organized representation of colour in macaque cortical area V2. Nature 421:535–539.

Xin YP, Koester J, Jing J, Weiss KR, Kupfermann I (2001) Cerebral-abdominal interganglionic coordinating neurons in Aplysia. J Neurophysiol 85:174–186.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Xu J, Gannon PJ, Emmorey K, Smith JF, Braun AR (2009) Symbolic gestures and spoken language are processed by a common neural system. Proc Natl Acad Sci USA 106:20664–20669.

Yamaguchi A, Kelley DB (2000) Generating sexually differentiated vocal patterns: Laryngeal nerve and EMG recordings from vocalizing male and female African clawed frogs (Xenopus laevis). J Neurosci 20:1559–1567.

Yamamoto K, Vernier P (2011) The evolution of dopamine systems in chordates. Front Neuroanat 5:21.

Yanai I, Peshkin L, Jorgensen P, Kirschner MW (2011) Mapping gene expression in two Xenopus species: Evolutionary constraints and developmental flexibility. Dev Cell 20: 483–496.

Yartsev MM, Witter MP, Ulanovsky N (2011) Grid cells without theta oscillations in the entorhinal cortex of bats. Nature 479:103–107.

Yonow N (1990) Red Sea Opisthobranchia, 3: The orders Sacoglossa, Cephalaspidea, and Nudibranchia: Doridacea (Mollusca, Opisthobranchia). Fauna Saudi Arabia 11:286–299.

Yopak KE, Lisney TJ, Darlington RB, Collin SP, Montgomery JC, Finlay BL (2010) A conserved pattern of brain scaling from sharks to primates. Proc Natl Acad Sci USA 107: 12946–12951.

Yotsu-Yamashita M, Nishimori K, Nitanai Y, Isemura M, Sugimoto A, Yasumoto T (2000) Binding properties of (3)H-PbTx-3 and (3)H-saxitoxin to brain membranes and to skeletal muscle membranes of puffer fish Fugu pardalis and the primary structure of a voltage-gated Na(+) channel alpha-subunit (fMNa1) from skeletal muscle of F. pardalis. Biochem Biophys Res Commun 267:403–412.

Young RM (1970) Mind, Brain and Adaptation in the Nineteenth Century (Clarendon Press, Oxford).

Yu YC, Bultje RS, Wang X, Shi SH (2009) Specific synapses develop preferentially among sister excitatory neurons in the neocortex. Nature 458:501–504.

Zakon HH, Lu Y, Zwickl DJ, Hillis DM (2006) Sodium channel genes and the evolution of diversity in communication signals of electric fishes: Convergent molecular evolution. Proc Natl Acad Sci USA 103:3675–3680.

Zakon HH, Jost MC, Lu Y (2011) Expansion of voltage-dependent Na+ channel gene family in early tetrapods coincided with the emergence of terrestriality and increased brain complexity. Mol Biol Evol 28:1415–1424.

Zalc B, Goujet D, Colman D (2008) The origin of the myelination program in vertebrates. Curr Biol 18:R511–R512.

Zelenitsky DK, Therrien F, Ridgely RC, McGee AR, Witmer LM (2011) Evolution of olfaction in non-avian theropod dinosaurs and birds. Proc Biol Sci 278:3625–3634.

Zguricas J, Bakker WF, Heus H, Lindhout D, Heutink P, Hovius SE (1998) Genetics of limb development and congenital hand malformations. Plast Reconstr Surg 101:1126–1135.

Zhang K, Sejnowski TJ (2000) A universal scaling law between gray matter and white matter of cerebral cortex. Proc Natl Acad Sci USA 97:5621–5626.

Zhang J, Webb DM, Podlaha O (2002a) Accelerated protein evolution and origins of human-specific features: Foxp2 as an example. Genetics 162:1825–1835.

Zhang J, Zhang YP, Rosenberg HF (2002b) Adaptive evolution of a duplicated pancreatic ribonuclease gene in a leaf-eating monkey. Nat Genet 30:411–415.

Zhang LI, Bao S, Merzenich MM (2001) Persistent and specific influences of early acoustic environments on primary auditory cortex. Nat Neurosci 4:1123–1130.

Zhang SP, Bandler R, Davis PJ (1995) Brain stem integration of vocalization: Role of the nucleus retroambigualis. J Neurophysiol 74:2500–2512.

Zhang YE, Landback P, Vibranovski MD, Long M (2011) Accelerated recruitment of new brain development genes into the human genome. PLoS Biol 9:e1001179.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.

Zhao FC, Zhu MY, Hu SX (2010) Community structure and composition of the Cambrian Chengjiang biota. Sci China Earth Sci 53:1784–1799.

Zhou W, Chung I, Liu Z, Goldin AL, Dong K (2004) A voltage-gated calcium-selective channel encoded by a sodium channel-like gene. Neuron 42:101–112.

Zimmer RK, Ferrer RP (2007) Neuroecology, chemical defense, and the keystone species concept. Biol Bull 213:208–225.

Zook JM (2007) Somatosensory adaptations of flying mammals. In Evolution of Nervous systems, eds Kaas J, Krubitzer L (Academic Press, San Diego, CA), Vol 3.

Zornik E, Katzen AW, Rhodes HJ, Yamaguchi A (2010) NMDAR-dependent control of call duration in Xenopus laevis. J Neurophysiol 103:3501–3515.

Zornik E, Kelley DB (2007) Breathing and calling: Neuronal networks in the Xenopus laevis hindbrain. J Comp Neurol 501:303–315.

Zorzi M, Priftis K, Umiltà C (2002) Brain damage: Neglect disrupts the mental number line. Nature 417:138–139.

Zottoli SJ (1977) Correlation of the startle reflex and Mauthner cell auditory responses in unrestrained goldfish. J Exp Biol 66:243–254.

Zuckerkandl E, Pauling LB (1962) Molecular disease, evolution, and genetic heterogeneity. In Horizons in Biochemistry, eds Kasha M, Pullman B (Academic Press, New York), pp 189-255.

Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Suggested Citation:'References.' National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
Next: Index »