Body size, brain size, and sexual dimorphism in Homo naledi from the Dinaledi Chamber

2017 ◽  
Vol 111 ◽  
pp. 119-138 ◽  
Author(s):  
Heather M. Garvin ◽  
Marina C. Elliott ◽  
Lucas K. Delezene ◽  
John Hawks ◽  
Steven E. Churchill ◽  
...  
2001 ◽  
Vol 79 (5) ◽  
pp. 759-765 ◽  
Author(s):  
Andrew N Iwaniuk

A possible relationship between sexual dimorphism in brain size and mating system was investigated in five ground squirrel species: Spermophilus lateralis, S. tridecemlineatus, S. richardsonii, S. columbianus, and S. parryii. Relative brain size was measured by determining the endocranial volume of 247 ground squirrel skulls and regressing these values against two measurements of body size: mass and length. Analyses of covariation in the brain size / body size relationship within the five species revealed that sexual brain-size dimorphism occurs in three of the five species: S. lateralis, S. richardsonii, and S. tridecemlineatus. Application of a reduced major axis regression model indicated, however, that only S. lateralis and S. richardsonii exhibit significant sexual brain-size dimorphism. These findings suggest that the degree of sexual brain-size dimorphism is not directly correlated with variation in mating systems. Spatial abilities may play a role in the evolution of sexual brain-size dimorphism in ground squirrels, but the spatial requirements of mating systems appear to be insufficient. The possibility of sex differences in cognition, resource competition, and other variables as contributory factors to the evolution of sexual brain-size dimorphism is offered, but detailed knowledge of sex differences in the behaviour of ground squirrels is required to provide a definitive answer.


2021 ◽  
pp. 1-12
Author(s):  
Carel P. van Schaik ◽  
Zegni Triki ◽  
Redouan Bshary ◽  
Sandra A. Heldstab

Both absolute and relative brain sizes vary greatly among and within the major vertebrate lineages. Scientists have long debated how larger brains in primates and hominins translate into greater cognitive performance, and in particular how to control for the relationship between the noncognitive functions of the brain and body size. One solution to this problem is to establish the slope of cognitive equivalence, i.e., the line connecting organisms with an identical bauplan but different body sizes. The original approach to estimate this slope through intraspecific regressions was abandoned after it became clear that it generated slopes that were too low by an unknown margin due to estimation error. Here, we revisit this method. We control for the error problem by focusing on highly dimorphic primate species with large sample sizes and fitting a line through the mean values for adult females and males. We obtain the best estimate for the slope of circa 0.27, a value much lower than those constructed using all mammal species and close to the value expected based on the genetic correlation between brain size and body size. We also find that the estimate of cognitive brain size based on cognitive equivalence fits empirical cognitive studies better than the encephalization quotient, which should therefore be avoided in future studies on primates and presumably mammals and birds in general. The use of residuals from the line of cognitive equivalence may change conclusions concerning the cognitive abilities of extant and extinct primate species, including hominins.


2014 ◽  
Vol 154 (2) ◽  
pp. 259-269 ◽  
Author(s):  
Heather M. Garvin ◽  
Sabrina B. Sholts ◽  
Laurel A. Mosca
Keyword(s):  

Author(s):  
Romain Willemet

The idea that allometry in the context of brain evolution mainly result from constraints channelling the scaling of brain components is deeply embedded in the field of comparative neurobiology. Constraints, however, only prevent or limit changes, and cannot explain why these changes happen in the first place. In fact, considering allometry as a lack of change may be one of the reasons why, after more than a century of research, there is still no satisfactory explanatory framework for the understanding of species differences in brain size and composition in mammals. The present paper attempts to tackle this issue by adopting an adaptationist approach to examine the factors behind the evolution of brain components. In particular, the model presented here aims to explain the presence of patterns of covariation among brain components found within major taxa, and the differences between taxa. The key determinant of these patterns of covariation within a taxon-cerebrotype (groups of species whose brains present a number of similarities at the physiological and anatomical levels) seems to be the presence of taxon-specific patterns of selection pressures targeting the functional and structural properties of neural components or systems. Species within a taxon share most of the selection pressures, but their levels scale with a number of factors that are often related to body size. The size and composition of neural systems respond to these selection pressures via a number of evolutionary scenarios, which are discussed here. Adaptation, rather than, as generally assumed, developmental or functional constraints, thus appears to be the main factor behind the allometric scaling of brain components. The fact that the selection pressures acting on the size of brain components form a pattern that is specific to each taxon accounts for the peculiar relationship between body size, brain size and composition, and behavioural capabilities characterizing each taxon. While it is important to avoid repeating the errors of the “Panglossian paradigm”, the elements presented here suggests that an adaptationist approach may shed a new light on the factors underlying, and the functional consequences of, species differences in brain size and composition.


2015 ◽  
Vol 282 (1810) ◽  
pp. 20151008 ◽  
Author(s):  
Kristina Noreikiene ◽  
Gábor Herczeg ◽  
Abigél Gonda ◽  
Gergely Balázs ◽  
Arild Husby ◽  
...  

The mosaic model of brain evolution postulates that different brain regions are relatively free to evolve independently from each other. Such independent evolution is possible only if genetic correlations among the different brain regions are less than unity. We estimated heritabilities, evolvabilities and genetic correlations of relative size of the brain, and its different regions in the three-spined stickleback ( Gasterosteus aculeatus ). We found that heritabilities were low (average h 2 = 0.24), suggesting a large plastic component to brain architecture. However, evolvabilities of different brain parts were moderate, suggesting the presence of additive genetic variance to sustain a response to selection in the long term. Genetic correlations among different brain regions were low (average r G = 0.40) and significantly less than unity. These results, along with those from analyses of phenotypic and genetic integration, indicate a high degree of independence between different brain regions, suggesting that responses to selection are unlikely to be severely constrained by genetic and phenotypic correlations. Hence, the results give strong support for the mosaic model of brain evolution. However, the genetic correlation between brain and body size was high ( r G = 0.89), suggesting a constraint for independent evolution of brain and body size in sticklebacks.


2017 ◽  
Vol 65 (5) ◽  
pp. 292 ◽  
Author(s):  
Bradley P. Smith ◽  
Teghan A. Lucas ◽  
Rachel M. Norris ◽  
Maciej Henneberg

Endocranial volume was measured in a large sample (n = 128) of free-ranging dingoes (Canis dingo) where body size was known. The brain/body size relationship in the dingoes was compared with populations of wild (Family Canidae) and domestic canids (Canis familiaris). Despite a great deal of variation among wild and domestic canids, the brain/body size of dingoes forms a tight cluster within the variation of domestic dogs. Like dogs, free-ranging dingoes have paedomorphic crania; however, dingoes have a larger brain and are more encephalised than most domestic breeds of dog. The dingo’s brain/body size relationship was similar to those of other mesopredators (medium-sized predators that typically prey on smaller animals), including the dhole (Cuon alpinus) and the coyote (Canis latrans). These findings have implications for the antiquity and classification of the dingo, as well as the impact of feralisation on brain size. At the same time, it highlights the difficulty in using brain/body size to distinguish wild and domestic canids.


2019 ◽  
pp. 261-336
Author(s):  
Georg F. Striedter ◽  
R. Glenn Northcutt

Early amniotes evolved water-resistant skin and eggs, which allowed them to live and reproduce entirely on land. Roughly 300 million years ago, amniotes split into synapsids (including mammals) and sauropsids (“reptiles” and birds). The sauropsid lineage includes squamates (lizards and snakes), turtles, and archosaurs (crocodilians and dinosaurs, including birds). Tympanic ears and more complex auditory systems evolved at least twice within the various amniote lineages. Amniotes also evolved a separate vomeronasal epithelium and more diverse modes of locomotion and feeding. Brain size relative to body size increased in early amniotes and then increased further in several amniote lineages, notably mammals and birds. The most enlarged regions were the cerebellum and the telencephalon. Within the telencephalon, sauropsids enlarged mainly the ventral pallium, whereas mammals enlarged the dorsal pallium (aka neocortex). Although these regions are not homologous to one another, they both receive unimodal auditory, visual, and somatosensory input from the thalamus.


2003 ◽  
Vol 117 (2) ◽  
pp. 236 ◽  
Author(s):  
John A. Virgl ◽  
Shane P. Mahoney ◽  
Kim Mawhinney

It is well recognized that differences in environmental selection pressures among populations can generate phenotypic divergence in a suite of morphological characteristics and associated life history traits. Previous analysis of mitochondrial DNA and body size have suggested that Black Bears (Ursus americanus) inhabiting the island of Newfoundland represent a different subspecies or ecotype from mainland populations. Assuming that body size covaries positively with skull size, we predicted that skull size would be greater for bears on the island than the mainland, and the distribution of size-related shape components in multivariate space should show a distinct separation between Newfoundland and mainland populations. Measurements of 1080 specimens from Newfoundland, Alberta, New York, and Quebec did not provide unequivocal support for our prediction that skull size in Newfoundland bears would be larger than bears from the mainland populations. After removing ontogenetic effects of skull size, between-population variation in skull shape was greater in females than males, and the analysis significantly separated Newfoundland bears from mainland populations. Explanations for this pattern are numerous, but currently remain hypothetical. Limited covariation between skull size and body size suggests that genetic traits regulating the size of Black Bear skulls are more heritable (i.e., less influenced by environmental selection pressures) than characteristics affecting body size. We hypothesize that if gape size does not limit prey size in solitary terrestrial carnivores, large degrees of among-population variation in body size should be coupled with little covariation in skull size. In general, sexual dimorphism in skull size and shape was marginal for the phenotypic characters measured in our study. We believe that sexual dimorphism in skull size in Black Bears is primarily driven by intrasexual selection in males for increased gape size display, while similarity in skull shape between sexes is associated with the constraints of a temporally-selective, but similar diet.


2020 ◽  
Vol 95 (2) ◽  
pp. 113-122
Author(s):  
Diego Ocampo ◽  
César Sánchez ◽  
Gilbert Barrantes

The ratio of brain size to body size (relative brain size) is often used as a measure of relative investment in the brain in ecological and evolutionary studies on a wide range of animal groups. In birds, a variety of methods have been used to measure the brain size part of this ratio, including endocranial volume, fixed brain mass, and fresh brain mass. It is still unclear, however, whether these methods yield the same results. Using data obtained from fresh corpses and from published sources, this study shows that endocranial volume, mass of fixed brain tissue, and fresh mass provide equivalent estimations of brain size for 48 bird families, in 19 orders. We found, however, that the various methods yield significantly different brain size estimates for hummingbirds (Trochilidae). For hummingbirds, fixed brain mass tends to underestimate brain size due to reduced tissue density, whereas endocranial volume overestimates brain size because it includes a larger volume than that occupied by the brain.


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