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The timing and nature of evolutionary shifts in the relative brain size of Primates have been extensively studied. Less is known, however, about the scaling of the brain-to-body size in their closest living relatives, i.e. among other members of Euarchontoglires (Dermoptera, Scandentia, Lagomorpha, Rodentia). Ordinary least squares (OLS), reduced major axis (RMA), and phylogenetic generalized least squares (PGLS) regressions were fitted to the largest euarchontogliran data set of brain and body mass, comprising 715 species. Contrary to previous inferences, lagomorph brain sizes (PGLS slope = 0.465; OLS slope = 0.593) scale relative to body mass similarly to rodents (PGLS = 0.526; OLS = 0.638), and differently than primates (PGLS = 0.607; OLS = 0.794). There is a shift in the pattern of the scaling of the brain in Primates, with Strepsirrhini occupying an intermediate stage similar to Scandentia but different from Rodentia and Lagomorpha, while Haplorhini differ from all other groups in the OLS and RMA analyses. The unique brain–body scaling relationship of Primates among Euarchontoglires illustrates the need for clade-specific metrics for relative brain size (i.e. encephalization quotients; EQs) for more restricted taxonomic entities than Mammalia. We created clade-specific regular and phylogenetically adjusted EQ equations at superordinal, ordinal, and subordinal levels. When using fossils as test cases, our results show that generalized mammalian equations underestimate the encephalization of the stem lagomorph Megalagus turgidus in the context of lagomorphs, overestimate the encephalization of the stem primate Microsyops annectens and the early euprimate Necrolemur antiquus , but provide similar EQ values as our new strepsirrhine-specific EQ when applied to the early euprimate Adapis parisiensis. [ABSTRACT FROM AUTHOR]

Objectives Evolutionary changes in hominin social complexity have been associated with increases in absolute brain size. The temporal lobes are nestled in the middle cranial fossae (MCF) of the skull, the dimensions of which allow estimation of temporal lobe volume (TLV) in extant and fossil taxa. Materials and Methods The main aim of this study is to determine where along the hominid phylogeny, major temporal lobe size transitions occurred. We used computed tomography (CT) scans of crania, 3D photogrammetry data, and laser surface scans of endocranial casts to measure seven MCF metrics in 11 extant anthropoid taxa using multiple regressions to estimate TLV in 5 extant hominids and 10 fossil hominins. Phylogenetic comparative methods mapped temporal lobe size, brain size, and temporal lobe proportions onto phylogenetic trees broadly for Hominidae and specifically for Hominini. Results Extant Homo sapiens were not an outlier in relative brain size, temporal lobe size, or proportions of the temporal lobes, but some proportions within the lobe were uniquely altered. The most notable changes in relative temporal lobe size and proportions saw a decrease in relative temporal lobe size and proportions in the genus Pan compared to other extant great apes and fossil hominins while there was a relative increase in the temporal lobe width and length in Australopithecus–Paranthropus clade compared to the genus Homo and other extant great apes including modern humans. Discussion We do not find support for the social brain, environmental or functional craniology hypotheses alone but think it prudent to consider the implications of cerebral reorganization between the temporal lobes and other regions of the brain within the context of these hypotheses and with future investigation is warranted. [ABSTRACT FROM AUTHOR]

Urban bird species represent a subset of the regional species pool, consisting of species that have been able to survive in, or colonise, urban areas. Urban birds are typically resident non-forest species with a broad diet and nesting high in trees or in cavities, and some studies have also claimed that they are large-brained. However, little is known about how urban bird communities change over time. Does the urban environment impose specific selective pressures favouring particular species or ecological groups, or do birds in urban areas simply have population changes reflecting population trends at larger scales? We assessed population changes of 45 breeding land bird species in Oslo, the capital of Norway, based on surveys conducted ca. 15 years apart. Population changes within Oslo most closely matched changes occurring at the regional level (national population trends from Norway and Sweden). Thus, species increasing in Oslo were those that also increased at the regional level. We found no evidence that relative brain size, diet or habitat preferences influenced population trends. However, controlling for regional population trends, there were additional residual effects of nest site and migration: species nesting on the ground or low in bushes had more positive changes than species nesting high in trees or in cavities, and resident species did better than long- or short-distance migrants. These results indicate that urban environments are not isolated islands only influenced by own selection pressures, but are connected with regional population dynamics, most likely through immigration. [ABSTRACT FROM AUTHOR]

Food hoarding provides animals access to resources during periods of scarcity. Studies on mammalian caching indicate associations with brain size, seasonality and diet but are biased to a subset of rodents. Whether the behaviour is generalizable at other taxonomic scales and/or is influenced by other ecological factors is less understood. Population density may influence food caching due to food competition or pilferage, but this remains untested in a comparative framework.Using phylogenetic analyses, we assessed the role of morphology (body and brain size), climate, diet breadth and population density on food caching behaviour evolution at multiple taxonomic scales. We also used a long‐term dataset on caching behaviour of red squirrels (Tamiasciurus fremonti) to test key factors (climate and population density) on hoarding intensity.Consistent with previous smaller scale studies, we found the mammalian ancestral state for food caching was larderhoarding, and scatterhoarding was derived. Caching strategy was strongly associated with brain size, population density and climate. Mammals with larger brains and hippocampal volumes were more likely to scatterhoard, and species living at higher population densities and in colder climates were more likely to larderhoard.Finer‐scale analyses within families, sub‐families and tribes indicated that the behaviour is evolutionary labile. Brain size in family Sciuridae and tribe Marmotini was larger in scatterhoarders, but not in other tribes. Scatterhoarding in tribe Marmotini was more likely in species with lower population densities while scatterhoarding in tribe Sciurini was associated with warmer climates. Red squirrel larderhoarding intensity was positively related to population density but not climate, implicating food competition or pilferage as an important mechanism mediating caching behaviour.Our results are consistent with previous smaller‐scale studies on food caching and indicate the evolutionary patterns of mammalian food caching are broadly generalizable. Given the lability of caching behaviour as evidenced by the variability of our results at finer phylogenetic scales, comparative analyses must consider taxonomic scale.Applying our results to conservation could prove useful as changes in population density or climate may select for different food caching strategies and thus can inform management of threatened and endangered species and their habitats. [ABSTRACT FROM AUTHOR]

It is well-established that brain size is associated with intelligence. But the relationship between cortical morphometric measures and intelligence is unclear. Studies have produced conflicting results or no significant relations between intelligence and cortical morphometric measures such as cortical thickness and peri-cortical contrast. This discrepancy may be due to multicollinearity amongst the independent variables in a multivariate regression analysis, or a failure to fully account for the relationship between brain size and intelligence in some other way. Our study shows that neither cortical thickness nor peri-cortical contrast reliably improves IQ prediction accuracy beyond what is achieved with brain volume alone. We show this in multiple datasets, with child data, developmental data, and with adult data; we show this with data acquired either at multiple sites, or at a single site; we show this with data acquired with different MRI scanner manufacturers, or with all data acquired on a single scanner; and we show this with fluid intelligence, full-scale IQ, performance IQ, and verbal IQ. But our point is not really even about IQ; rather we proffer a methodological caveat and potential explanation of the discrepancies in previous results, and which applies broadly. [ABSTRACT FROM AUTHOR]

Diets fed to commercial chicken breeders are high in n-6 fatty acids (n-6 FAs) and low in n-3 fatty acids (n-3 FAs). N-3 FAs are essential for embryonic brain development. In precocial birds, like chickens, brain development and brain n- 3 FA accrual occur primarily before hatching. In two experiments, broiler and layer breeders were fed diets with or without flaxseed as the source of n-3 FAs from plant-based alpha-linolenic acid. Day-old broiler (n = 80) and layer (n = 96) offspring were dissected to calculate the percentage brain-to-body weight. Brain FA analyses from total lipid extracts were determined in the broiler (n = 24) and layer (n = 24) offspring brains, and the percentage FA composition and concentration (µg FAs per g brain) were calculated for each n-3 and n-6 FA. The brain size was only increased in broiler offspring from mothers fed flaxseed (χ² = 9.22, p = 0.002). In layer offspring only, the maternal flaxseed diet increased the brain concentration and percentage of n-3 FAs and decreased n-6 FAs (p < 0.05). We showed that feeding flaxseed to mothers increased the brain size in broiler offspring and altered brain FA composition in layer offspring. These results may have implications for poultry and other captive bird species fed diets low in n-3 FAs. [ABSTRACT FROM AUTHOR]

A leading hypothesis for the evolution of large brains in humans and other species is that a feedback loop exists whereby intelligent animals forage more efficiently, which results in increased energy intake that fuels the growth and maintenance of large brains. We test this hypothesis for the first time with high-resolution tracking data from four sympatric, frugivorous rainforest mammal species (42 individuals) and drone-based maps of their predominant feeding trees. We found no evidence that larger-brained primates had more efficient foraging paths than smaller brained procyonids. This refutes a key assumption of the fruit-diet hypothesis for brain evolution, suggesting that other factors such as temporal cognition, extractive foraging or sociality have been more important for brain evolution. [ABSTRACT FROM AUTHOR]

Introduction: Crested chickens show abnormalities in their anatomy of the skull, endocranium, and brain (including cerebral elongation) and can be appropriate model systems for neuroanatomical evolution, brain-skull integration, and skull and brain deformities. Here, we give a detailed comprehensive description of the skull of crested chickens using the example of the Padovana chicken, including ontogenetic aspects and an allometric analysis of their brain size. Methods: In total, 109 chickens of two different strains of the Padovana chicken were hatched together. All animals were X-rayed weekly during growth. Nine juvenile (ready for hatch) and 22 adult skulls were processed for histology and morphological descriptions, and a further 20 individuals were processed for brain analysis. Results: At hatching, all chicks were already crested, and a distinctive bony protuberance was first observed at the age of 4 weeks. Juvenile chickens exhibit either an open neurocranium or a protuberance. In the adult skull, foramina of different sizes can be found in the frontal bone, but no completely open neurocrania are observed in juveniles. Particularly in Padovana with cranial protuberances, several peculiarities can be observed in the os mesethmoidale, os nasale, os praemaxillare, orbit, and cranial fossae. Additionally, the brain of Padovana with cranial protuberances looks drawn in length with the shape of an hourglass and showed significantly larger encephalization indices than plain-headed breeds, topped only by another crested chicken breed. Discussion: Investigations on chickens with cerebral elongation may facilitate the understanding of skull and brain dysplasia and may provide meaningful insights into cerebral hernia development. Additionally, crested breeds, combined with standard chickens, form a promising comparative system for investigating the emergence of novel brain and skull morphologies. [ABSTRACT FROM AUTHOR]

Amniotes differ substantially in absolute and relative brain size after controlling for allometry, and numerous hypotheses have been proposed to explain brain size evolution. Brain size is thought to correlate with processing capacity and the brain's ability to support complex manipulation such as nest‐building skills. The increased complexity of nest structure is supposed to be a measure of an ability to manipulate nesting material into the required shape. The degree of nest‐structure complexity is also supposed to be associated with body mass, partly because small species lose heat faster and delicate and insulated nests are more crucial for temperature control of eggs during incubation by small birds. Here, we conducted comparative analyses to test these hypotheses by investigating whether the complexity of species‐typical nest structure can be explained by brain size and body mass (a covariate also to control for allometric effects on brain size) across 1353 bird species from 147 families. Consistent with these hypotheses, our results revealed that avian brain size increases as the complexity of the nest structure increases after controlling for a significant effect of body size, and also that a negative relationship exists between nest complexity and body mass. [ABSTRACT FROM AUTHOR]

Agricultural intensification reduces the taxonomic diversity of bird communities, but its influence on functional diversity has been less studied. Here, we analyze the response of functional diversity of different cereal farmland bird communities across Europe to a gradient of agricultural intensification. We collected bibliographical information on life history traits (i.e. body mass, brain size, age of sexual maturity, clutch size, number of clutches, lifespan) of 30 species of birds recorded during field surveys in eight European countries. The index ''brood value'' was calculated to know each species’ level of reproductive investment per clutch. Intensification gradients at two spatial scales were obtained from field data through PCA, related to management practices at the field scale and the variation in structure and composition of farmland at the landscape scale respectively. We calculated the functional diversity index (FD) and the community-weighted mean (CWM) for each trait and sampling area, and linear mixed models in relation to the two intensification gradients were performed. Results showed that stronger intensification at the field level favors the assembly of shorter-lived communities and bird species with smaller relative brain sizes, also decreasing overall trait diversity. It also restricts the range of strategies for parental investment, reducing the functional diversity of the brood value index. More intensive field management would favor bird communities dominated by generalist and even introduced and/or managed hunting species, while putting at risk those farmland- and grassland-adapted species, typically more associated with the provision of ecosystem services. This highlights the relevance of field management (agrochemicals use, ploughing frequency) for the functional composition of bird communities and the conservation of farmland biodiversity. These findings add to existing knowledge on how species’ pace of life and cognitive capacity interact with drivers of global change, such as agricultural intensification.

• Agricultural intensification affects life history and functional trait diversity of farmland bird communities. • We calculated the functional diversity index and the community-weighted mean for six life history traits and the brood value index of 30 bird species in eight European farmland areas. • Stronger agricultural intensification at the field level (agrochemicals use, ploughing frequency) favors the assembly of shorter-lived communities and bird species with smaller relative brain sizes. Agricultural intensification reduces the taxonomic diversity of bird communities, but its influence on functional diversity has been less studied. Here, we analyze the response of functional diversity of different cereal farmland bird communities across Europe to a gradient of agricultural intensification. We collected bibliographical information on life history traits (i.e. body mass, brain size, age of sexual maturity, clutch size, number of clutches, lifespan) of 30 species of birds recorded during field surveys in eight European countries. The index "brood value" was calculated to know each species' level of reproductive investment per clutch. Intensification gradients at two spatial scales were obtained from field data through PCA, related to management practices at the field scale and the variation in structure and composition of farmland at the landscape scale respectively. We calculated the functional diversity index (FD) and the community-weighted mean (CWM) for each trait and sampling area, and linear mixed models in relation to the two intensification gradients were performed. Results showed that stronger intensification at the field level favors the assembly of shorter-lived communities and bird species with smaller relative brain sizes, also decreasing overall trait diversity. It also restricts the range of strategies for parental investment, reducing the functional diversity of the brood value index. More intensive field management would favor bird communities dominated by generalist and even introduced and/or managed hunting species, while putting at risk those farmland- and grassland-adapted species, typically more associated with the provision of ecosystem services. This highlights the relevance of field management (agrochemicals use, ploughing frequency) for the functional composition of bird communities and the conservation of farmland biodiversity. These findings add to existing knowledge on how species' pace of life and cognitive capacity interact with drivers of global change, such as agricultural intensification. [ABSTRACT FROM AUTHOR]

Morphometric studies of 3D micro CT‐scanned images can provide insights into the evolution of the brain and sensory structures but such data are still scarce for the most diverse mammalian order of rodents. From reviewed and new data, we tested for convergence to extreme aridity and high elevation in the sensory and brain morphology of rodents, from morphometric data from micro‐CT X‐ray scans of 174 crania of 16 species of three distantly related African murid (soft‐furred mice, Praomyini, laminate‐toothed rats, Otomyini, and gerbils, Gerbillinae) clades and one North American cricetid (deer mice and white‐footed mice, Peromyscus) clade. Recent studies demonstrated convergent evolution acting on the oval window area of the cochlea (enlarged in extremely arid‐adapted species of Otomyini and Gerbillinae) and on endocranial volume (reduced in high elevation taxa of Otomyini and Peromyscus). However, contrary to our predictions, we did not find evidence of convergence in brain structure to aridity, or in the olfactory/respiratory system (turbinate bones) to high elevation. Brain structure differed, particularly in the petrosal lobules of the cerebellum and the olfactory bulbs, between Otomyini and Gerbillinae, with extreme arid‐adapted species in each clade being highly divergent (not convergent) from other species in the same clade. We observed greater "packing" of the maxillary turbinate bones, which have important respiratory functions, in Peromyscus mice from high and low elevations compared to the high‐elevation African Praomyini, but more complex patterns within Peromyscus, probably related to trade‐offs in respiratory physiology and heat exchange in the nasal epithelium associated with high‐elevation adaptation. [ABSTRACT FROM AUTHOR]

Here, we investigate the relationship between relative brain size and sexual weapons in ruminants. In most cases, sexual weaponry is heavily male-biased, and costs resulting from growing, maintaining, or wielding weapons are suffered primarily by males. We used phylogenetic comparative analyses to test whether increased investment in sexual weapon size (tusks, antlers, and horns) across four families (Tragulidae, Moschidae, Cervidae, and Bovidae) was associated with decrease in relative brain size and whether the difference in weapon investment relative to conspecific females led to sexual differences in relative brain size. We found no relationship between relative brain size and relative weapon size within males or females, but when we compared males directly to conspecific females, we found that as males invested more in larger weaponry relative to females, they had smaller brain sizes relative to females, regardless of weapon type. Our findings suggest greater investment in some types of elaborate weapons in males, and larger brain sizes in females. We discuss the possibility that larger brain sizes in females could be due to female sociality, lower investment in weaponry, or enhancing female assessment of male traits. Significance statement: We took measurements of antlers, horns, and tusks from skulls of both males and females, as well as brain volume and looked at the relationship between relative weapon size and relative brain size. Our work found support that bearing large, exaggerated sexually selected weapons results in a sexually dimorphic relationship with relative brain size: when males invest more in sexual weaponry, females invest more in relative brain size. Given that most studies largely are focused on tradeoffs solely within one sex, our study compares the relationship between sexes to measure sexual dimorphic investment. The evolution of weaponry in ruminants is one of the most widely studied topics of the last 70 years and this study yields new support for the possible presence of sexual dimorphic trade-offs amongst sexually selected traits. [ABSTRACT FROM AUTHOR]

Diets fed to commercial chicken breeders are high in n-6 fatty acids (n-6 FAs) and low in n-3 fatty acids (n-3 FAs). N-3 FAs are essential for embryonic brain development. In precocial birds, like chickens, brain development and brain n-3 FA accrual occur primarily before hatching. In two experiments, broiler and layer breeders were fed diets with or without flaxseed as the source of n-3 FAs from plant-based alpha-linolenic acid. Day-old broiler (n = 80) and layer (n = 96) offspring were dissected to calculate the percentage brain-to-body weight. Brain FA analyses from total lipid extracts were determined in the broiler (n = 24) and layer (n = 24) offspring brains, and the percentage FA composition and concentration (µg FAs per g brain) were calculated for each n-3 and n-6 FA. The brain size was only increased in broiler offspring from mothers fed flaxseed (χ2 = 9.22, p = 0.002). In layer offspring only, the maternal flaxseed diet increased the brain concentration and percentage of n-3 FAs and decreased n-6 FAs (p < 0.05). We showed that feeding flaxseed to mothers increased the brain size in broiler offspring and altered brain FA composition in layer offspring. These results may have implications for poultry and other captive bird species fed diets low in n-3 FAs.

IntroductionCrested chickens show abnormalities in their anatomy of the skull, endocranium, and brain (including cerebral elongation) and can be appropriate model systems for neuroanatomical evolution, brain–skull integration, and skull and brain deformities. Here, we give a detailed comprehensive description of the skull of crested chickens using the example of the Padovana chicken, including ontogenetic aspects and an allometric analysis of their brain size.MethodsIn total, 109 chickens of two different strains of the Padovana chicken were hatched together. All animals were X-rayed weekly during growth. Nine juvenile (ready for hatch) and 22 adult skulls were processed for histology and morphological descriptions, and a further 20 individuals were processed for brain analysis.ResultsAt hatching, all chicks were already crested, and a distinctive bony protuberance was first observed at the age of 4 weeks. Juvenile chickens exhibit either an open neurocranium or a protuberance. In the adult skull, foramina of different sizes can be found in the frontal bone, but no completely open neurocrania are observed in juveniles. Particularly in Padovana with cranial protuberances, several peculiarities can be observed in the os mesethmoidale, os nasale, os praemaxillare, orbit, and cranial fossae. Additionally, the brain of Padovana with cranial protuberances looks drawn in length with the shape of an hourglass and showed significantly larger encephalization indices than plain-headed breeds, topped only by another crested chicken breed.DiscussionInvestigations on chickens with cerebral elongation may facilitate the understanding of skull and brain dysplasia and may provide meaningful insights into cerebral hernia development. Additionally, crested breeds, combined with standard chickens, form a promising comparative system for investigating the emergence of novel brain and skull morphologies.

Abstract Vertebrate brains show extensive variation in relative size. The expensive brain hypothesis argues that one important source of this variation is linked to a species’ ability to generate the energy required to sustain the brain, especially during periods of unavoidable food scarcity. Here we ask whether this hypothesis, tested so far in endothermic vertebrates, also applies to ectotherms, where ambient temperature is an additional major aspect of energy balance. Phylogenetic comparative analyses of reptiles and amphibians support the hypothesis. First, relative brain size increases with higher body temperature in those species active during the day that can gain free energy by basking. Second, relative brain size is smaller among nocturnal species, which generally face less favorable energy budgets, especially when maintaining high body temperature. However, we do not find an effect of seasonal variation in ambient temperature or food on brain size, unlike in endotherms. We conclude that the factors affecting energy balance in ectotherms and endotherms are overlapping but not identical. We therefore discuss the idea that when body temperatures are seasonally very low, cognitive benefits may be thwarted and selection on larger brain size may be rare. Indeed, mammalian hibernators may show similarities to ectotherms.

Higher cognition in humans, compared to other primates, is often attributed to an increased brain size, especially forebrain cortical surface area. Brain size is determined through highly orchestrated developmental processes, including neural stem cell proliferation, dierentiation, migration, lamination, arborization, and apoptosis. Disruption in these processes often results in either a small (microcephaly) or large (megalencephaly) brain. One of the key mechanisms controlling these developmental processes is the spatial and temporal transcriptional regulation of critical genes. In humans, microcephaly is defined as a condition with a significantly smaller head circumference compared to the average head size of a given age and sex group. A growing number of genes are identified as associated with microcephaly, and among them are those involved in transcriptional regulation. In this review, a subset of genes encoding transcription factors (e.g., homeobox-, basic helix-loop-helix-, forkhead box-, high mobility group box-, and zinc finger domain-containing transcription factors), whose functions are important for cortical development and implicated in microcephaly, are discussed. [ABSTRACT FROM AUTHOR]

Greater longevity, slower maturation and shorter birth intervals are life history features that distinguish humans from the other living members of our hominid family, the great apes. Theory and evidence synthesized here suggest the evolution of those features can explain both our bigger brains and our cooperative sociality. I rely on Sarah Hrdy's hypothesis that survival challenges for ancestral infants propelled the evolution of distinctly human socioemotional appetites and Barbara Finlay and colleagues' findings that mammalian brain size is determined by developmental duration. Similar responsiveness to varying developmental contexts in chimpanzee and human one-year-olds suggests similar infant responsiveness in our nearest common ancestor. Those ancestral infants likely began to acquire solid food while still nursing and fed themselves at weaning as chimpanzees and other great apes do now. When human ancestors colonized habitats lacking foods that infants could handle, dependents' survival became contingent on subsidies. Competition to engage subsidizers selected for capacities and tendencies to enlist and maintain social connections during the early wiring of expanding infant brains with lifelong consequences that Hrdy labeled "emotionally modern" social cognition. [ABSTRACT FROM AUTHOR]

Environmental seasonality can promote the evolution of larger brains through cognitive and behavioral flexibility but can also hamper it when temporary food shortage is buffered by stored energy. Multiple hypotheses linking brain evolution with resource acquisition and allocation have been proposed for warm-blooded organisms, but it remains unclear how these extend to cold-blooded taxa whose metabolism is tightly linked to ambient temperature. Here, we integrated these hypotheses across frogs and toads in the context of varying brumation (hibernation) durations and their environmental correlates. We showed that protracted brumation covaried negatively with brain size but positively with reproductive investment, likely in response to brumation-dependent changes in the socio-ecological context and associated selection on different tissues. Our results provide novel insights into resource allocation strategies and possible constraints in trait diversification, which may have important implications for the adaptability of species under sustained environmental change.

In some species, permanent curtailment of reproduction part‐way through the lifespan of adult females is a feature of their evolved life history. The existence of such a post‐reproductive life stage is apparently rare; reasonably robust evidence for this is confined to only six species (humans, Asian elephants and four whales). That it occurs at all appears to contradict our view of natural selection operating to maximize fitness and special circumstances must exist to explain its occurrence. We evaluate the main hypotheses posited to explain the evolution of this life stage, why it occurs in a restricted group of animals, and why only in females. We bring together literature from multiple biological disciplines and levels of enquiry, ranging through evolutionary ecology, developmental biology, physiology, neuroscience, molecular biology, and human medicine. We conclude that while time‐limited fertility is not in itself adaptive, the duration of subsequent survival is likely to be linked to inclusive fitness benefits. We present a new hypothesis which posits that the duration of female fertility in certain long‐lived, highly encephalised species, with no post‐natal oogenesis, is limited by the need for intense screening of oocyte mitochondria. This is required to support endothermy coupled with the very high energy requirement for the development and maintenance of the exceptionally large brain size required for complex social living. This limits the number and shelf‐life of oocytes, creating an antagonistically pleotropic effect that is beneficial to the production of high performing offspring but carries the later life cost of time‐limited female fertility. But the end of the fertile period is no time to die. Inclusive fitness benefits arising from protracted parental care of offspring, overlapping generations, and kin group structures means that continued survival of post‐reproductive females is favoured by selection. We suggest further lines of research to test these ideas. [ABSTRACT FROM AUTHOR]

Uncovering relationships between neuroanatomy, behavior, and evolution are important for understanding the factors that control brain function. Voluntary exercise is one key behavior that both affects, and may be affected by, neuroanatomical variation. Moreover, recent studies suggest an important role for physical activity in brain evolution. We used a unique and ongoing artificial selection model in which mice are bred for high voluntary wheel-running behavior, yielding four replicate lines of high runner (HR) mice that run ∼3-fold more revolutions per day than four replicate nonselected control (C) lines. Previous studies reported that, with body mass as a covariate, HR mice had heavier whole brains, non-cerebellar brains, and larger midbrains than C mice. We sampled mice from generation 66 and used high-resolution microscopy to test the hypothesis that HR mice have greater volumes and/or cell densities in nine key regions from either the midbrain or limbic system. In addition, half of the mice were given 10 weeks of wheel access from weaning, and we predicted that chronic exercise would increase the volumes of the examined brain regions via phenotypic plasticity. We replicated findings that both selective breeding and wheel access increased total brain mass, with no significant interaction between the two factors. In HR compared to C mice, adjusting for body mass, both the red nucleus (RN) of the midbrain and the hippocampus (HPC) were significantly larger, and the whole midbrain tended to be larger, with no effect of wheel access nor any interactions. Linetype and wheel access had an interactive effect on the volume of the periaqueductal gray (PAG), such that wheel access increased PAG volume in C mice but decreased volume in HR mice. Neither linetype nor wheel access affected volumes of the substantia nigra, ventral tegmental area, nucleus accumbens, ventral pallidum (VP), or basolateral amygdala. We found no main effect of either linetype or wheel access on neuronal densities (numbers of cells per unit area) for any of the regions examined. Taken together, our results suggest that the increased exercise phenotype of HR mice is related to increased RN and hippocampal volumes, but that chronic exercise alone does not produce such phenotypes. [ABSTRACT FROM AUTHOR]

Insular populations of mammals have been shown to undergo drastic morphological changes relative to mainland counterparts, and these adaptations can provide insight into the evolutionary effects of predation and competition. Selection has been shown to favor more energetically efficient body plans in insular mammals, even when this entails the reduction of anti-predator defenses, but few studies have focused on morphological effects within the same species. Previous research has established that insular large mammals tend to reduce in body size, and that size reduction may not scale isometrically across all body parts. The brain has been a particular subject of interest due to its high energy requirements. Here, we report that an extant, dwarfed island population of black-tailed deer (Odocoileus hemionus columbianus) exhibits significantly reduced brain mass relative to body mass in comparison to their mainland conspecifics, with brain mass 4.9% smaller in the island population for a given body mass. Further, in the dwarfed population, orbital area was 4.1% smaller for a given body mass, but this reduction was not significant. Foramina magna reduced isometrically. In resource-limited insular environments, negative allometry of the brain is consistent with predictions of reduced investment in energetically costly organs. This study is, to our knowledge, the first to examine the morphological effects of insularity on brain size in two conspecific populations, and these findings suggest that selection toward reduced brain size may act relatively quickly after isolation. [ABSTRACT FROM AUTHOR]

Changes to the environmental landscapes from the Eocene to Holocene have influenced the evolution of Cercopithecoidea from arboreal origins in wet, forested regions in the Early Oligocene Fayum to semi-terrestrial lifestyles in drier Neogene landscapes and social systems of larger group living. These eco-behavioural transitions likely accompanied changes in behaviour, brain function, and associated skull morphology. The temporal lobe of the brain, an association cortex, is in close proximity to the middle cranial fossa (MCF) allowing prediction of temporal lobe volume (TLV) and investigation of cerebral reorganisation. We used micro-computed tomography (µCT) cranial scans (n = 135) generated into 3D virtual crania with seven MCF metrics predicting TLV from a multiple regression of 11 extant anthropoid taxa. We studied eight extinct taxa Proteopithecus sylviae and Catopithecus browni from the Late Eocene, Early Oligocene Apidium phiomense, Parapithecus grangeri and Aegyptopithecus zeuxis, Middle Miocene Victoriapithecus macinnesi, Pliocene Dinopithecus ingens, Pleistocene Papio angusticeps, and extant cercopithecines Cercocebus atys, Macaca mulatta and Papio anubis. PGLS regressions examined relative TLV to brain size between extinct and extant taxa. We tested differences in slopes and intercepts between extinct and extant cercopithecoids with statistically significant differences in slopes but not the intercepts, with stem-anthropoids having relative smaller TLV for brain size compared to extant cercopithecoids. Potential drivers for temporal lobe evolution include paleoenvironmental shifts from Eocene tropical rainforests to Plio-Pleistocene savannas. Socio-behavioural implications include change from arboreal to semi-terrestrial lifestyles, higher visual acuity, larger group sizes and greater cognitive complexity. [ABSTRACT FROM AUTHOR]

Simple Summary: Parrots (Order: Psittaciformes) are an ancient arboreal lineage with a long history as companion animals for humans. Since at least the 1960s, released parrots have become established in non-native ranges globally. The method of their introduction is almost certainly a direct result of the pet trade through either accidental or intentional releases. Within the continental United States there are currently seventy-three naturalized parrot species that have been observed as of May 2023. Of these, close to half have established breeding populations. The propensity for a parrot species to become established appears to be phylogenetically driven. Notably, parrots in the family Cacatuidae and Neotropical Pyrrhua are less successful at establishing themselves in the United States once released. We posit that what makes parrots such successful naturalized species are their charismatic nature paired with considerable intelligence and behavioral flexibility. Parrots (Order: Psittaciformes) represent one of the most striking and ecomorphologically diverse avian clades, spanning more than two orders of magnitude in body size with populations occupying six continents. The worldwide diaspora of parrots is largely due to the pet trade, driven by human desire for bright, colorful, and intelligent animals as companions. Some introduced species have aptly inserted themselves into the local ecosystem and established successful breeding colonies all around the globe. Notably, the United States is home to several thriving populations of introduced species including red-masked parakeets (Psittacara erythrogenys), monk parakeets (Myiopsitta monachus), nanday conures (Aratinga nenday), and red-crowned amazons (Amazona viridigenalis). Their incredible success globally begs the question as to how these birds adapt so readily to novel environments. In this commentary, we trace parrots through evolutionary history, contextualize existent naturalized parrot populations within the contiguous United States, and provide a phylogenetic regression analysis of body mass and brain size based on success in establishing breeding populations. The propensity for a parrot species to become established appears to be phylogenetically driven. Notably, parrots in the family Cacatuidae and Neotropical Pyrrhua appear to be poor at establishing themselves in the United States once released. Although brain size among Psittaciformes did not show a significant impact on successful breeding in the continental United States, we propose that the success of parrots can be attributed to their charismatic nature, significant intelligence relative to other avian lineages, and behavioral flexibility. [ABSTRACT FROM AUTHOR]

Domestication is a well-known example of the relaxation of environmentally based cognitive selection that leads to reductions in brain size. However, little is known about how brain size evolves after domestication and whether subsequent directional/artificial selection can compensate for domestication effects. The first animal to be domesticated was the dog, and recent directional breeding generated the extensive phenotypic variation among breeds we observe today. Here we use a novel endocranial dataset based on high-resolution CT scans to estimate brain size in 159 dog breeds and analyze how relative brain size varies across breeds in relation to functional selection, longevity, and litter size. In our analyses, we controlled for potential confounding factors such as common descent, gene flow, body size, and skull shape. We found that dogs have consistently smaller relative brain size than wolves supporting the domestication effect, but breeds that are more distantly related to wolves have relatively larger brains than breeds that are more closely related to wolves. Neither functional category, skull shape, longevity, nor litter size was associated with relative brain size, which implies that selection for performing specific tasks, morphology, and life history does not necessarily influence brain size evolution in domesticated species. [ABSTRACT FROM AUTHOR]

Ever since the availability of genomes from Neanderthals, Denisovans, and ancient humans, the field of evolutionary genomics has been searching for protein-coding variants that may hold clues to how our species evolved over the last ∼600,000 years. In this study, we identify such variants in the human-specific NOTCH2NL gene family, which were recently identified as possible contributors to the evolutionary expansion of the human brain. We find evidence for the existence of unique protein-coding NOTCH2NL variants in Neanderthals and Denisovans which could affect their ability to activate Notch signaling. Furthermore, in the Neanderthal and Denisovan genomes, we find unusual NOTCH2NL configurations, not found in any of the modern human genomes analyzed. Finally, genetic analysis of archaic and modern humans reveals ongoing adaptive evolution of modern human NOTCH2NL genes, identifying three structural variants acting complementary to drive our genome to produce a lower dosage of NOTCH2NL protein. Because copy-number variations of the 1q21.1 locus, encompassing NOTCH2NL genes, are associated with severe neurological disorders, this seemingly contradicting drive toward low levels of NOTCH2NL protein indicates that the optimal dosage of NOTCH2NL may have not yet been settled in the human population.

Little is known about the cognitive abilities of bears, despite possessing relatively large brains for their body size. One reason this group is perhaps overlooked is because they are thought to fail to conform to the “social brain” hypothesis, by being relatively solitary species but still possessing large brains. Here, to better understand the proposed benefits afforded by encephalization, the cognitive abilities of 17 captive European brown bears Ursus arctos arctos were tested. The aim was to determine whether bears possess problem-solving and object-manipulation abilities. Two experimental tests – a puzzle box and an object-manipulation set-up – were presented to bears at seven UK zoological parks. Generalised linear mixed models were used to determine which variables, specifically age, sex, motivational levels, behavioral diversity and persistence, influence cognitive performance. Results revealed evidence of trial-and-error learning; however, two juveniles appeared to acquire a latch association, suggesting some individuals have potential to adopt successful strategies and draw perceptive associations. Individual variation in motivation levels appears to be an important factor influencing cognitive performance. Overall, the bears failed to spontaneously use a tool but still managed to retrieve the food reward, instead using alternative techniques to solve the problem. Analyses revealed both age and sex to be negatively associated with time-to-solve in our sample, indicating the younger male bears solved the task more quickly. Results suggest social dynamics of group-living bears to be influencing cognitive performance, as the collective nature of testing resulted in increased competition over a high-value reward. These results are discussed herein. Brown bears are confirmed to be an excellent model species for testing the cognitive abilities of Ursids, as well as theories of cognitive evolution.

Simple Summary: Birds often exhibit differences in locomotion, foraging, and predator detection, many of which are often reflected in their eye sizes. Therefore, understanding the coevolutionary relationships between eye size and ecological factors, behaviours and brain size in birds is essential. Our results indicate that species with larger eye sizes reside in dense habitats, feed on invertebrates or vertebrates and have larger brains, suggesting that habitat openness, food type and cognition play critical roles in shaping visual sensitivity and resolution. However, we did not find any correlation between eye size and migration behaviour or foraging habitat, indicating that these factors are likely not major drivers of eye size evolution. The eye is the primary sensory organ that obtains information from the ecological environments and specifically bridges the brain with the extra environment. However, the coevolutionary relationships between eye size and ecological factors, behaviours and brain size in birds remain poorly understood. Here, we investigate whether eye size evolution is associated with ecological factors (e.g., habitat openness, food type and foraging habitat), behaviours (e.g., migration and activity pattern) and brain size among 1274 avian species using phylogenetically controlled comparative analyses. Our results indicate that avian eye size is significantly associated with habitat openness, food type and brain size. Species living in dense habitats and consuming animals exhibit larger eye sizes compared to species living in open habitats and consuming plants, respectively. Large-brained birds tend to possess larger eyes. However, migration, foraging habitat and activity pattern were not found to be significantly associated with eye size in birds, except for nocturnal birds having longer axial lengths than diurnal ones. Collectively, our results suggest that avian eye size is primarily influenced by light availability, food need and cognitive ability. [ABSTRACT FROM AUTHOR]

Harmful algal blooms (HABs) release toxic compounds in water and are increasing in frequency worldwide. The neurotoxin β-methylamino- l -alanine (BMAA) is released by HABs and has garnered much attention over the past 20 years due to its association with human neurodegenerative disorders, but its effects on wildlife are still largely unknown. This study characterized the effects of chronic exposure to environmentally relevant concentrations of BMAA on the behavior and brain size of developing zebrafish (Danio rerio). Zebrafish were continuously exposed to 0, 1, 10, or 100 µg/l waterborne BMAA between 0- and 5-days postfertilization (dpf) before the onset of exogenous feeding. At 5 dpf, locomotion and responses to vibrational and visual stimuli were assessed. Following behavioral testing, larvae body and brain size were measured. Survival between 0 and 5 dpf did not differ between treatments. Moreover, BMAA exposure did not affect thigmotaxis, startle response magnitude, habituation to repeated presentation of vibrational startling stimuli, or relative brain size. A moderate increase in overall activity was observed in larvae exposed to 10 μg/l BMAA under light, but this effect was not seen in dark conditions, indicating that visual processing may have been affected by chronic BMAA exposure. Thus, passive continuous exposure to environmentally relevant concentrations of BMAA prior to first feeding in zebrafish did not affect survival or selected measures used to represent brain development, anxiety, and motor reflexes, but a limited light-dependent effect on locomotion suggests targeted neurotoxicity within the visual system. [ABSTRACT FROM AUTHOR]

A typical consequence of breeding animal species for domestication is a reduction in relative brain size. When domesticated animals escape from captivity and establish feral populations, the larger brain of the wild phenotype is usually not regained. In the American mink (Neovison vison), we found an exception to this rule. We confirmed the previously described reduction in relative braincase size and volume compared to their wild North American ancestors in mink bred for their fur in Poland, in a dataset of 292 skulls. We then also found a significant regrowth of these measures in well-established feral populations in Poland. Closely related, small mustelids are known for seasonal reversible changes in skull and brain size. It seems that these small mustelids are able to regain the brain size, which is adaptive for living in the wild, and flexibly respond to selection accordingly.

The underpinnings of mild to moderate neurodevelopmental delay remain elusive, often leading to late diagnosis and interventions. Here, we present data on exome and genome sequencing as well as array analysis of 13 individuals that point to pathogenic, heterozygous, mostly de novo variants in WDFY3 (significant de novo enrichment P = 0.003) as a monogenic cause of mild and non-specific neurodevelopmental delay. Nine variants were protein-truncating and four missense. Overlapping symptoms included neurodevelopmental delay, intellectual disability, macrocephaly, and psychiatric disorders (autism spectrum disorders/attention deficit hyperactivity disorder). One proband presented with an opposing phenotype of microcephaly and the only missense-variant located in the PH-domain of WDFY3. Findings of this case are supported by previously published data, demonstrating that pathogenic PH-domain variants can lead to microcephaly via canonical Wnt-pathway upregulation. In a separate study, we reported that the autophagy scaffolding protein WDFY3 is required for cerebral cortical size regulation in mice, by controlling proper division of neural progenitors. Here, we show that proliferating cortical neural progenitors of human embryonic brains highly express WDFY3, further supporting a role for this molecule in the regulation of prenatal neurogenesis. We present data on Wnt-pathway dysregulation in Wdfy3-haploinsufficient mice, which display macrocephaly and deficits in motor coordination and associative learning, recapitulating the human phenotype. Consequently, we propose that in humans WDFY3 loss-of-function variants lead to macrocephaly via downregulation of the Wnt pathway. In summary, we present WDFY3 as a novel gene linked to mild to moderate neurodevelopmental delay and intellectual disability and conclude that variants putatively causing haploinsufficiency lead to macrocephaly, while an opposing pathomechanism due to variants in the PH-domain of WDFY3 leads to microcephaly.

Purpose: To analyze the relationship between blood pressure (BP) variables, including circadian pattern, and cognition in 90+ year-olds. Methods: Twenty-four hour ambulatory BP monitoring was completed on 121 participants drawn from a longitudinal study of aging and dementia in the oldest-old. Various measures of BP and its variability, including nocturnal dipping, were calculated. Each person was given both a neuropsychological test battery covering different cognitive domains and a neurological examination to determine cognitive status. Seventy-one participants had a brain magnetic resonance imaging (MRI) scan. Results: Participants ranged in age from 90 to 102 years (mean = 93), about two-thirds were female, and nearly 80% had at least some college education. Mean nocturnal dips differed significantly between cognitively normal (n = 97) and impaired individuals (n = 24), with cognitively normal participants having on average greater nocturnal dips [6.6% vs. 1.3%, p = 0.006 for systolic BP (SBP); 11% vs. 4.4%, p = 0.002 for diastolic BP (DBP)]. Nocturnal dips were also related to performance on select cognitive test scores (especially those related to language, recent memory and visual-spatial ability), with individuals who performed below previously established median norms having significantly smaller nocturnal dips (both SBP and DBP) than those above the median. DBP reverse dippers had larger mean white matter hyperintensities (WMH as percent of total brain volume; 1.7% vs. 1.2%, 1.1% and 1.0% in extreme dippers, dippers, non-dippers) and a greater proportion had lobar cerebral microbleeds (CMBs; 44% vs. 0%, 7%, 16%, p < 0.05). Impaired participants had higher mean WMH than those with normal cognition (1.6% vs. 1.0% p = 0.03) and more tended to have CMB (31% vs. 20%, p = n.s.). Conclusion: These findings suggest that cognitive dysfunction is associated with dysregulation in the normal circadian BP pattern. Further study is warranted of the potential role of WHM and CMB as mediators of this association.

Extra‐pair paternity (EPP) benefits to improve the reproductive success via extra‐pair fertilizations without the costs of parental care in males and through improved offspring quality with additional food and parental care in females among species of birds. Variations in the EPP appear to link to behavioral and ecological factors and sexual selection. According to the "relationship intelligence hypothesis", the cognitive abilities of the birds play an important role in maintaining long‐term relationships. Here, we undertook the first comparative test of the relationships between extra‐pair paternity and brain size, testis size, and life histories among 315 species of birds using phylogenetically controlled comparative analyses and path analysis. After controlling for the effects of shared ancestry and body mass, the frequency of EPP was negatively correlated with relative brain size, but positively with testis size across species of birds. However, the frequency of EPP was not linked to life‐history traits (e.g. incubation period, fledging period, clutch size, egg mass, and longevity). Our findings suggest that large‐brained birds associated with enhanced cognitive abilities are more inclined to maintain long‐term stable relationships with their mates and to mutualism with them than to increase the frequency of EPP. [ABSTRACT FROM AUTHOR]

Whether head size and/or biological sex influence proxies of white matter (WM) microstructure such as fractional anisotropy (FA) and mean diffusivity (MD) remains controversial. Diffusion tensor imaging (DTI) indices are also associated with age, but there are large discrepancies in the spatial distribution and timeline of age‐related differences reported. The aim of this study was to evaluate the associations between intracranial volume (ICV), sex, and age and DTI indices from WM in a population‐based study of healthy individuals (n = 812) aged 50–66 in the Nord‐Trøndelag health survey. Semiautomated tractography and tract‐based spatial statistics (TBSS) analyses were performed on the entire sample and in an ICV‐matched sample of men and women. The tractography results showed a similar positive association between ICV and FA in all major WM tracts in men and women. Associations between ICV and MD, radial diffusivity and axial diffusivity were also found, but to a lesser extent than FA. The TBSS results showed that both men and women had areas of higher and lower FA when controlling for age, but after controlling for age and ICV only women had areas with higher FA. The ICV matched analysis also demonstrated that only women had areas of higher FA. Age was negatively associated with FA across the entire WM skeleton in the TBSS analysis, independent of both sex and ICV. Combined, these findings demonstrated that both ICV and sex contributed to variation in DTI indices and emphasized the importance of considering ICV as a covariate in DTI analysis. [ABSTRACT FROM AUTHOR]

Brain size evolution in hominins constitutes a crucial evolutionary trend, yet the underlying mechanisms behind those changes are not well understood. Here, climate change is considered as an environmental factor using multiple paleoclimate records testing temperature, humidity, and precipitation against changes to brain size in 298 Homo specimens over the past fifty thousand years. Across regional and global paleoclimate records, brain size in Homo averaged significantly lower during periods of climate warming as compared to cooler periods. Geological epochs displayed similar patterns, with Holocene warming periods comprising significantly smaller brained individuals as compared to those living during glacial periods at the end of the Late Pleistocene. Testing spatiotemporal patterns, the adaptive response appears to have started roughly fifteen thousand years ago and may persist into modern times. To a smaller degree, humidity and precipitation levels were also predictive of brain size, with arid periods associated with greater brain size in Homo. The findings suggest an adaptive response to climate change in human brain size that is driven by natural selection in response to environmental stress. [ABSTRACT FROM AUTHOR]

The extent to which the evolution of a larger brain is adaptive remains controversial. Trinidadian killifish (Anablepsoides hartii) are found in sites that differ in predation intensity; fish that experience decreased predation and increased intraspecific competition exhibit larger brains. We evaluated the connection between brain size and fitness (survival and growth) when killifish are found in their native habitats and when fish are transplanted from sites with predators to high‐competition sites that lack predators. Selection for a larger brain was absent within locally adapted populations. Conversely, there was a strong positive relationship between brain size and growth in transplanted but not resident fish in high‐competition environments. We also observed significantly larger brain sizes in the transplanted fish that were recaptured at the end of the experiment versus those that were not. Our results provide experimental support that larger brains increase fitness and are favoured in high‐competition environments. [ABSTRACT FROM AUTHOR]

Typically, investigations of animal cognition couple careful experimental manipulations with examination of the animal's behavioural responses. Sometimes those questions have included attempts to describe the neural underpinnings of the behavioural outputs. Over the past 25 years, behaviours that involve spatial learning and memory (such as navigation and food storing) has been one context in which such dual or correlated investigations have been both accessible and productive. Here I review some of that work and where it has led. Because of the wealth of data and insights gained from that work and song learning before it, it seems that it might also be useful to try to add some neurobiology to other systems in animal cognition. I finish then, with a description of recent work on the cognition and neurobiology of avian nest building. It is still relatively early days but asking questions about the cognition of nest building has already shown both neural correlates of nest building and that learning and memory play a much greater role in this behaviour than previously considered. While it is not yet clear how putting these components together will be synergistic, the examples of song learning and food storing provide encouragement. Perhaps this might be true for other behaviours too? [ABSTRACT FROM AUTHOR]

Conflicting theories have been proposed to explain variation in relative brain size across the animal kingdom. Ecological theories argue that the cognitive demands of seasonal or unpredictable environments have selected for increases in relative brain size, whereas the 'social brain hypothesis' argues that social complexity is the primary driver of brain size evolution. Here, we use a comparative approach to test the relative importance of ecology (diet, foraging niche and migration), sociality (social bond, cooperative breeding and territoriality) and developmental mode in shaping brain size across 1886 bird species. Across all birds, we find a highly significant effect of developmental mode and foraging niche on brain size, suggesting that developmental constraints and selection for complex motor skills whilst foraging generally imposes important selection on brain size in birds. We also find effects of social bonding and territoriality on brain size, but the direction of these effects do not support the social brain hypothesis. At the same time, we find extensive heterogeneity among major avian clades in the relative importance of different variables, implying that the significance of particular ecological and social factors for driving brain size evolution is often clade‐ and context‐specific. Overall, our results reveal the important and complex ways in which ecological and social selection pressures and developmental constraints shape brain size evolution across birds. [ABSTRACT FROM AUTHOR]

The current article advances the hypothesis that creative culture evolved, in part, to allay the costs of the overgrown human brain and the cognitive integration limit that it imposes. Specific features can be expected among cultural elements best suited to allaying the integration limit and also among the neurocognitive mechanisms that might undergird these cultural effects. Music, visual art, and meditation are used as examples to illustrate how culture helps to bridge or sidestep the integration limit. Tiered religious, philosophical, and psychological concepts are considered in light of their reflection of the tiered process of cognitive integration. The link between creativity and mental illness is offered as additional support for the role of cognitive disconnection as a wellspring of cultural creativity, and I propose that this link can be harnessed in defense of neurodiversity. Developmental and evolutionary implications of the integration limit are discussed. [ABSTRACT FROM AUTHOR]

Morphological traits, such as white patches, floppy ears and curly tails, are ubiquitous in domestic animals and are referred to as the ‘domestication syndrome’. A commonly discussed hypothesis that has the potential to provide a unifying explanation for these traits is the ‘neural crest/domestication syndrome hypothesis’. Although this hypothesis has the potential to explain most traits of the domestication syndrome, it only has an indirect connection to the reduction of brain size, which is a typical trait of domestic animals. We discuss how the expensive-tissue hypothesis might help explain brain-size reduction in domestication.

Abstract Many biological traits covary with body size, resulting in an allometric relationship. Identifying the evolutionary drivers of these traits is complicated by possible relationships between a candidate selective agent and body size itself, motivating the widespread use of multiple regression analysis. However, the possibility that multiple regression may generate misleading estimates when predictor variables are correlated has recently received much attention. Here, we argue that a primary source of such bias is the failure to account for the complex causal structures underlying brains, bodies, and agents. When brains and bodies are expected to evolve in a correlated manner over and above the effects of specific agents of selection, neither simple nor multiple regression will identify the true causal effect of an agent on brain size. This problem results from the inclusion of a predictor variable in a regression analysis that is (in part) a consequence of the response variable. We demonstrate these biases with examples and derive estimators to identify causal relationships when traits evolve as a function of an existing allometry. Model mis‐specification relative to plausible causal structures, not collinearity, requires further consideration as an important source of bias in comparative analyses.

Throughout the hominin lineage brain size is believed to have increased threefold – increase which, it is argued by some researchers, results in the enhanced brain power that distinguishes humans from any other living being. However, as we demonstrate in this article this supposed increase is the result of comparing the species mean of contemporary humans with other great apes and fossil hominins. This method obscures both interpopulational variation among modern humans, and the fact that the putative increases in the mean are the result of an increase in the upper limit in some populations, which has the result of obscuring the relative stasis in the lower limit over the last 600k years. For example, populations such as Aboriginal Australians have a range that is more different from Danes than it is from that of Asian H. erectus over the last 600ka. Yet Aboriginal Australians, whose unique anatomy seems to be related to the climatic conditions of Australia, possess all of the socio-cognitive traits characteristic of all other modern-day populations – yet they seemed not to have undergone increase in brain size to the degree that many other populations have. In this instance brain size seems to be unrelated to cognition. In this article we present a statistical analysis of interpopulational variation in contemporary humans and why such an analysis is crucial for our understanding of hominin cognitive, social and technological evolution. We also suggest how such variation may add to our understanding of hominin ontogeny or life history. Additionally, we develop a model based on humanity’s unique form of embodied social cognition that results from our upright bipedal posture and hand morphology. This model is then used to explain the results of our statistical analysis and the possible factors underpinning the human emergence.

Brain size and cortical folding have increased and decreased recurrently during mammalian evolution. Identifying genetic elements whose sequence or functional properties co-evolve with these traits can provide unique information on evolutionary and developmental mechanisms. A good candidate for such a comparative approach is TRNP1, as it controls proliferation of neural progenitors in mice and ferrets. Here, we investigate the contribution of both regulatory and coding sequences of TRNP1 to brain size and cortical folding in over 30 mammals. We find that the rate of TRNP1 protein evolution (ω) significantly correlates with brain size, slightly less with cortical folding and much less with body size. This brain correlation is stronger than for >95% of random control proteins. This co-evolution is likely affecting TRNP1 activity, as we find that TRNP1 from species with larger brains and more cortical folding induce higher proliferation rates in neural stem cells. Furthermore, we compare the activity of putative cis-regulatory elements (CREs) of TRNP1 in a massively parallel reporter assay and identify one CRE that likely co-evolves with cortical folding in Old World monkeys and apes. Our analyses indicate that coding and regulatory changes that increased TRNP1 activity were positively selected either as a cause or a consequence of increases in brain size and cortical folding. They also provide an example how phylogenetic approaches can inform biological mechanisms, especially when combined with molecular phenotypes across several species.

Brain size is controlled by several factors during neuronal development, including neural progenitor proliferation, neuronal arborization, gliogenesis, cell death, and synaptogenesis. Multiple neurodevelopmental disorders have co-morbid brain size abnormalities, such as microcephaly and macrocephaly. Mutations in histone methyltransferases that modify histone H3 on Lysine 36 and Lysine 4 (H3K36 and H3K4) have been identified in neurodevelopmental disorders involving both microcephaly and macrocephaly. H3K36 and H3K4 methylation are both associated with transcriptional activation and are proposed to sterically hinder the repressive activity of the Polycomb Repressor Complex 2 (PRC2). During neuronal development, tri-methylation of H3K27 (H3K27me3) by PRC2 leads to genome wide transcriptional repression of genes that regulate cell fate transitions and neuronal arborization. Here we provide a review of neurodevelopmental processes and disorders associated with H3K36 and H3K4 histone methyltransferases, with emphasis on processes that contribute to brain size abnormalities. Additionally, we discuss how the counteracting activities of H3K36 and H3K4 modifying enzymes vs. PRC2 could contribute to brain size abnormalities which is an underexplored mechanism in relation to brain size control.

The brain is among the most energetically costly organs in vertebrates, and thus trade-offs have been hypothesized to exert constraints on brain size evolution. The energy trade-off hypothesis (ETH) predicts that reducing the energy consumption of reproduction or other costly tissues should compensate for the cost of a large brain. Egg production in birds requires a large proportion of the total energy budget, and a clutch mass in some bird species can outweigh the body mass of the female. To date, this hypothesis has mainly been tested in mammals and ectothermic animals such as anurans and fishes. We collated data on adult brain size, body mass and egg-production traits such as clutch size, egg mass and annual broods from published studies, and conducted a phylogenetic comparative test of the interplay between egg-production investment and brain size evolution across bird species. After controlling for phylogenetic relationships and body size, we find a negative correlation between brain size and clutch size across 1395 species, which favored ETH. However, when egg mass was integrated in models, positive associations were detected between brain size and mass of eggs (via egg mass, clutch mass and annual total egg mass). Our results suggest that brain size trades off against egg-production only via certain aspects (e.g., clutch size). By contrast, a positive relationship between brain size and total egg reproduction (e.g., clutch mass and annual total egg mass) implied increased total energy budget outweighing energy allocation across bird species. Our study shows that there is no general energy trade-off between brain size and egg-reproduction investment, and suggests that brain size evolution follows mixed strategies across bird species.

Comparative developmental studies provide growing understanding of vertebrate forebrain evolution. This short review directs the spotlight to some newly emerging aspects, including the evolutionary origin of the proliferative region known as the subventricular zone (SVZ) and of intermediate progenitor cells (IPCs) that populate the SVZ, neural circuits that originated within homologous regions across all amniotes, and the role of thermogenesis in the acquisition of an increased brain size. These data were presented at the 8th European Conference on Comparative Neurobiology.