scholarly journals Bigger is not always better: when brains get smaller

2005 ◽  
Vol 1 (3) ◽  
pp. 283-286 ◽  
Author(s):  
Kamran Safi ◽  
Marc A Seid ◽  
Dina K.N Dechmann

Many studies assume that an increase in brain size is beneficial. However, the costs of producing and maintaining a brain are high, and we argue that brain size should be secondarily reduced by natural selection whenever the costs outweigh the benefits. Our results confirm this by showing that brain size is subject to bidirectional selection. Relative to the ancestral state, brain size in bats has been reduced in fast flyers, while it has increased in manoeuvrable flyers adapted to flight in complex habitats. This study emphasizes that brain reduction and enlargement are equally important, and they should both be considered when investigating brain size evolution.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Manuel Will ◽  
Mario Krapp ◽  
Jay T. Stock ◽  
Andrea Manica

AbstractIncreasing body and brain size constitutes a key macro-evolutionary pattern in the hominin lineage, yet the mechanisms behind these changes remain debated. Hypothesized drivers include environmental, demographic, social, dietary, and technological factors. Here we test the influence of environmental factors on the evolution of body and brain size in the genus Homo over the last one million years using a large fossil dataset combined with global paleoclimatic reconstructions and formalized hypotheses tested in a quantitative statistical framework. We identify temperature as a major predictor of body size variation within Homo, in accordance with Bergmann’s rule. In contrast, net primary productivity of environments and long-term variability in precipitation correlate with brain size but explain low amounts of the observed variation. These associations are likely due to an indirect environmental influence on cognitive abilities and extinction probabilities. Most environmental factors that we test do not correspond with body and brain size evolution, pointing towards complex scenarios which underlie the evolution of key biological characteristics in later Homo.


2021 ◽  
Vol 17 (5) ◽  
pp. 20210023
Author(s):  
Michael P. Moore

Natural selection on juveniles is often invoked as a constraint on adult evolution, but it remains unclear when such restrictions will have their greatest impact. Selection on juveniles could, for example, mainly limit the evolution of adult traits that mostly develop prior to maturity. Alternatively, selection on juveniles might primarily constrain the evolution of adult traits that experience weak or context-dependent selection in the adult stage. Using a comparative study of dragonflies, I tested these hypotheses by examining how a species’ larval habitat was related to the evolution of two adult traits that differ in development and exposure to selection: adult size and male ornamentation. Whereas adult size is fixed at metamorphosis and experiences consistent positive selection in the adult stage, ornaments develop throughout adulthood and provide context-dependent fitness benefits. My results show that species that develop in less stable larval habitats have smaller adult sizes and slower rates of adult size evolution. However, these risky larval habitats do not limit ornament expression or rates of ornament evolution. Selection on juveniles may therefore primarily affect the evolution of adult traits that mostly develop prior to maturity.


Mammalia ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Ying Jiang ◽  
Jia Yu Wang ◽  
Xiao Fu Huang ◽  
Chun Lan Mai ◽  
Wen Bo Liao

Abstract Brain size exhibits significant changes within and between species. Evolution of large brains can be explained by the need to improve cognitive ability for processing more information in changing environments. However, brains are among the most energetically expensive organs. Enlarged brains can impose energetic demands that limit brain size evolution. The expensive tissue hypothesis (ETH) states that a decrease in the size of another expensive tissue, such as the gut, should compensate for the cost of a large brain. We studied the interplay between energetic limitations and brain size evolution in small mammals using phylogenetically generalized least squares (PGLS) regression analysis. Brain mass was not correlated with the length of the digestive tract in 37 species of small mammals after correcting for phylogenetic relationships and body size effects. We further found that the evolution of a large brain was not accompanied by a decrease in male reproductive investments into testes mass and in female reproductive investment into offspring number. The evolution of brain size in small mammals is inconsistent with the prediction of the ETH.


2016 ◽  
Vol 302 (1) ◽  
pp. 63-72 ◽  
Author(s):  
C. L. Mai ◽  
J. Liao ◽  
L. Zhao ◽  
S. M. Liu ◽  
W. B. Liao

2019 ◽  
Vol 69 (3) ◽  
pp. 265-279 ◽  
Author(s):  
Chun Lan Mai ◽  
Wen Bo Liao

Abstract Selection pressure is an important force in shaping the evolution of vertebrate brain size among populations within species as well as between species. The evolution of brain size is tightly linked to natural and sexual selection, and life-history traits. In particular, increased environmental stress, intensity of sexual selection, and slower life history usually result in enlarged brains. However, although previous studies have addressed the causes of brain size evolution, no systematic reviews have been conducted to explain brain size in anurans. Here, we review whether brain size evolution supports the cognitive buffer hypothesis (CBH), the expensive tissue hypothesis (ETH), or the developmental cost hypothesis (DCH) by analyzing the intraspecific and/or interspecific patterns in brain size and brain regions (i.e., olfactory nerves, olfactory bulbs, telencephalon, optic tectum, and cerebellum) associated with ecological factors (habitat, diet and predator risk), sexual selection intensity, life-history traits (age at sexual maturity, mean age, longevity, clutch size and egg size, testis size and sperm length), and other energetic organs. Our findings suggest that brain size evolution in anurans supports the CBH, ETH or DCH. We also suggest future directions for studying the relationships between brain size evolution and crypsis (i.e., ordinary mucous glands in the skin), and food alteration in different developmental stages.


2001 ◽  
Vol 24 (2) ◽  
pp. 278-279 ◽  
Author(s):  
Francisco Aboitiz

Finlay et al. address the importance of developmental constraints in brain size evolution. I discuss some aspects of this view such as the relation of brain size with processing capacity. In particular, I argue that in human evolution there must have been specific selection for increased processing capacity, and as a consequence for increased brain size.


2005 ◽  
Vol 18 (1) ◽  
pp. 223-237 ◽  
Author(s):  
A. P. Moller ◽  
J. Erritzoe ◽  
L. Z. Garamszegi
Keyword(s):  

2012 ◽  
Vol 63 (1) ◽  
pp. 52-63 ◽  
Author(s):  
Karin Isler ◽  
Carel P. van Schaik

BMC Biology ◽  
2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Joanna Baker ◽  
Andrew Meade ◽  
Chris Venditti

Abstract Background Testes vary widely in mass relative to body mass across species, but we know very little about which genes underlie and contribute to such variation. This is partly because evidence for which genes are implicated in testis size variation tends to come from investigations involving just one or a few species. Contemporary comparative phylogenetic methods provide an opportunity to test candidate genes for their role in phenotypic change at a macro-evolutionary scale—across species and over millions of years. Previous attempts to detect genotype-phenotype associations across species have been limited in that they can only detect where genes have driven directional selection (e.g. brain size increase). Results Here, we introduce an approach that uses rates of evolutionary change to overcome this limitation to test whether any of twelve candidate genes have driven testis size evolution across tetrapod vertebrates—regardless of directionality. We do this by seeking a relationship between the rates of genetic and phenotypic evolution. Our results reveal five genes (Alkbh5, Dmrtb1, Pld6, Nlrp3, Sp4) that each have played unique and complex roles in tetrapod testis size diversity. In all five genes, we find strong significant associations between the rate of protein-coding substitutions and the rate of testis size evolution. Such an association has never, to our knowledge, been tested before for any gene or phenotype. Conclusions We describe a new approach to tackle one of the most fundamental questions in biology: how do individual genes give rise to biological diversity? The ability to detect genotype-phenotype associations that have acted across species has the potential to build a picture of how natural selection has sculpted phenotypic change over millions of years.


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