scholarly journals The evolution of body size and shape in the human career

2016 ◽  
Vol 371 (1698) ◽  
pp. 20150247 ◽  
Author(s):  
William L. Jungers ◽  
Mark Grabowski ◽  
Kevin G. Hatala ◽  
Brian G. Richmond

Body size is a fundamental biological property of organisms, and documenting body size variation in hominin evolution is an important goal of palaeoanthropology. Estimating body mass appears deceptively simple but is laden with theoretical and pragmatic assumptions about best predictors and the most appropriate reference samples. Modern human training samples with known masses are arguably the ‘best’ for estimating size in early bipedal hominins such as the australopiths and all members of the genus Homo , but it is not clear if they are the most appropriate priors for reconstructing the size of the earliest putative hominins such as Orrorin and Ardipithecus . The trajectory of body size evolution in the early part of the human career is reviewed here and found to be complex and nonlinear. Australopith body size varies enormously across both space and time. The pre- erectus early Homo fossil record from Africa is poor and dominated by relatively small-bodied individuals, implying that the emergence of the genus Homo is probably not linked to an increase in body size or unprecedented increases in size variation. Body size differences alone cannot explain the observed variation in hominin body shape, especially when examined in the context of small fossil hominins and pygmy modern humans. This article is part of the themed issue ‘Major transitions in human evolution’.

2014 ◽  
Vol 112 (2) ◽  
pp. 366-371 ◽  
Author(s):  
Habiba Chirchir ◽  
Tracy L. Kivell ◽  
Christopher B. Ruff ◽  
Jean-Jacques Hublin ◽  
Kristian J. Carlson ◽  
...  

Humans are unique, compared with our closest living relatives (chimpanzees) and early fossil hominins, in having an enlarged body size and lower limb joint surfaces in combination with a relatively gracile skeleton (i.e., lower bone mass for our body size). Some analyses have observed that in at least a few anatomical regions modern humans today appear to have relatively low trabecular density, but little is known about how that density varies throughout the human skeleton and across species or how and when the present trabecular patterns emerged over the course of human evolution. Here, we test the hypotheses that (i) recent modern humans have low trabecular density throughout the upper and lower limbs compared with other primate taxa and (ii) the reduction in trabecular density first occurred in early Homo erectus, consistent with the shift toward a modern human locomotor anatomy, or more recently in concert with diaphyseal gracilization in Holocene humans. We used peripheral quantitative CT and microtomography to measure trabecular bone of limb epiphyses (long bone articular ends) in modern humans and chimpanzees and in fossil hominins attributed to Australopithecus africanus, Paranthropus robustus/early Homo from Swartkrans, Homo neanderthalensis, and early Homo sapiens. Results show that only recent modern humans have low trabecular density throughout the limb joints. Extinct hominins, including pre-Holocene Homo sapiens, retain the high levels seen in nonhuman primates. Thus, the low trabecular density of the recent modern human skeleton evolved late in our evolutionary history, potentially resulting from increased sedentism and reliance on technological and cultural innovations.


Author(s):  
N. Toledo ◽  
M.S. Bargo ◽  
S.F. Vizcaíno ◽  
G. De Iuliis ◽  
F. Pujos

ABSTRACTPilosa include anteaters (Vermilingua) and sloths (Folivora). Modern tree sloths are represented by two genera, Bradypus and Choloepus (both around 4–6 kg), whereas the fossil record is very diverse, with approximately 90 genera ranging in age from the Oligocene to the early Holocene. Fossil sloths include four main clades, Megalonychidae, Megatheriidae, Nothrotheriidae, and Mylodontidae, ranging in size from tens of kilograms to several tons. Modern Vermilingua are represented by three genera, Cyclopes, Tamandua and Myrmecophaga, with a size range from 0.25 kg to about 30 kg, and their fossil record is scarce and fragmentary. The dependence of the body size on phylogenetic pattern of Pilosa is analysed here, according to current cladistic hypotheses. Orthonormal decomposition analysis and Abouheif C-mean were performed. Statistics were significantly different from the null-hypothesis, supporting the hypothesis that body size variation correlates with the phylogenetic pattern. Most of the correlation is concentrated within Vermilingua, and less within Mylodontidae, Megatheriidae, Nothrotheriidae and Megalonychidae. Influence of basal metabolic rate (BMR), dietary habits and substrate preference is discussed. In anteaters, specialised insectivory is proposed as the primary constraint on body size evolution. In the case of sloths, mylodontids, megatheriids and nothrotheriids show increasing body size through time; whereas megalonychids retain a wider diversity of sizes. Interplay between BMR and dietary habits appears to be the main factor in shaping evolution of sloth body size.


2009 ◽  
Vol 276 (1661) ◽  
pp. 1469-1476 ◽  
Author(s):  
Shai Meiri ◽  
Tamar Dayan ◽  
Daniel Simberloff ◽  
Richard Grenyer

Evolutionary biologists have long been fascinated by both the ways in which species respond to ecological conditions at the edges of their geographic ranges and the way that species' body sizes evolve across their ranges. Surprisingly, though, the relationship between these two phenomena is rarely studied. Here, we examine whether carnivore body size changes from the interior of their geographic range towards the range edges. We find that within species, body size often varies strongly with distance from the range edge. However, there is no general tendency across species for size to be either larger or smaller towards the edge. There is some evidence that the smallest guild members increase in size towards their range edges, but results for the largest guild members are equivocal. Whether individuals vary in relation to the distance from the range edges often depends on the way edge and interior are defined. Neither geographic range size nor absolute body size influences the tendency of size to vary with distance from the range edge. Therefore, we suggest that the frequent significant association between body size and the position of individuals along the edge-core continuum reflects the prevalence of geographic size variation and that the distance to range edge per se does not influence size evolution in a consistent way.


2011 ◽  
Vol 7 (4) ◽  
pp. 558-561 ◽  
Author(s):  
Alexander L. Jaffe ◽  
Graham J. Slater ◽  
Michael E. Alfaro

Extant chelonians (turtles and tortoises) span almost four orders of magnitude of body size, including the startling examples of gigantism seen in the tortoises of the Galapagos and Seychelles islands. However, the evolutionary determinants of size diversity in chelonians are poorly understood. We present a comparative analysis of body size evolution in turtles and tortoises within a phylogenetic framework. Our results reveal a pronounced relationship between habitat and optimal body size in chelonians. We found strong evidence for separate, larger optimal body sizes for sea turtles and island tortoises, the latter showing support for the rule of island gigantism in non-mammalian amniotes. Optimal sizes for freshwater and mainland terrestrial turtles are similar and smaller, although the range of body size variation in these forms is qualitatively greater. The greater number of potential niches in freshwater and terrestrial environments may mean that body size relationships are more complicated in these habitats.


Author(s):  
Ricardo Wilches ◽  
William H Beluch ◽  
Ellen McConnell ◽  
Diethard Tautz ◽  
Yingguang Frank Chan

Abstract Most phenotypic traits in nature involve the collective action of many genes. Traits that evolve repeatedly are particularly useful for understanding how selection may act on changing trait values. In mice, large body size has evolved repeatedly on islands and under artificial selection in the laboratory. Identifying the loci and genes involved in this process may shed light on the evolution of complex, polygenic traits. Here, we have mapped the genetic basis of body size variation by making a genetic cross between mice from the Faroe Islands, which are among the largest and most distinctive natural populations of mice in the world, and a laboratory mouse strain selected for small body size, SM/J. Using this F2 intercross of 841 animals, we have identified 111 loci controlling various aspects of body size, weight and growth hormone levels. By comparing against other studies, including the use of a joint meta-analysis, we found that the loci involved in the evolution of large size in the Faroese mice were largely independent from those of a different island population or other laboratory strains. We hypothesize that colonization bottleneck, historical hybridization, or the redundancy between multiple loci have resulted in the Faroese mice achieving an outwardly similar phenotype through a distinct evolutionary path.


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 4 (1) ◽  
Author(s):  
Maggie M. Hantak ◽  
Bryan S. McLean ◽  
Daijiang Li ◽  
Robert P. Guralnick

AbstractAnthropogenically-driven climate warming is a hypothesized driver of animal body size reductions. Less understood are effects of other human-caused disturbances on body size, such as urbanization. We compiled 140,499 body size records of over 100 North American mammals to test how climate and human population density, a proxy for urbanization, and their interactions with species traits, impact body size. We tested three hypotheses of body size variation across urbanization gradients: urban heat island effects, habitat fragmentation, and resource availability. Our results demonstrate that both urbanization and temperature influence mammalian body size variation, most often leading to larger individuals, thus supporting the resource availability hypothesis. In addition, life history and other ecological factors play a critical role in mediating the effects of climate and urbanization on body size. Larger mammals and species that utilize thermal buffering are more sensitive to warmer temperatures, while flexibility in activity time appears to be advantageous in urbanized areas. This work highlights the value of using digitized, natural history data to track how human disturbance drives morphological variation.


2018 ◽  
Vol 49 (1) ◽  
pp. 379-408 ◽  
Author(s):  
Roger B.J. Benson

Dinosaurs were large-bodied land animals of the Mesozoic that gave rise to birds. They played a fundamental role in structuring Jurassic–Cretaceous ecosystems and had physiology, growth, and reproductive biology unlike those of extant animals. These features have made them targets of theoretical macroecology. Dinosaurs achieved substantial structural diversity, and their fossil record documents the evolutionary assembly of the avian body plan. Phylogeny-based research has allowed new insights into dinosaur macroevolution, including the adaptive landscape of their body size evolution, patterns of species diversification, and the origins of birds and bird-like traits. Nevertheless, much remains unknown due to incompleteness of the fossil record at both local and global scales. This presents major challenges at the frontier of paleobiological research regarding tests of macroecological hypotheses and the effects of dinosaur biology, ecology, and life history on their macroevolution.


2001 ◽  
Vol 268 (1476) ◽  
pp. 1589-1593 ◽  
Author(s):  
Louis J. D'Amico ◽  
Goggy Davidowitz ◽  
H. Frederik Nijhout

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