Nearly every modern Olympic Games has brought astonished comments and criticism of the body sizes of female gymnasts. The comments from laypersons, scientists, journalists, and physicians too often imply that these diminutive athletes are unusually small and possibly unhealthy. Purpose: An extended and updated analysis of the sizes of U.S. female Olympic gymnasts including the 2012 and 2016 Olympic Games. Methods: Official public records from the US Olympic Committee and USA Gymnastics of Olympic team members were assessed including height, mass, age, body-mass index (BMI) and team performance rankings. Sixteen Olympic teams with a total of 123 team positions including the alternates were assessed. Trend analyses were conducted using linear and polynomial models. Results: Analyses indicated that since 1956, height, mass, age, and BMI declined at first and then increased, with the exceptions of height and rank. Best regression fits were obtained via 2nd order polynomial equations. Height and rank showed a downward trend throughout the historical period. Conclusion: Female Olympic gymnasts were getting smaller through approximately the 1980s and early 1990s. An upward trend in size variables was then observed through 2008. The addition of the 2012 and 2016 Olympic Games data showed that height shifted to a decline from a slight upward trend, and rank continued to decline throughout the historical period.

Negative body image and preoccupation with weight are the norm for most women and girls in Western society, despite their potentially harmful consequences for psychological and physical wellness. While we know that many in this population experience negative feelings towards their bodies, we do not know if their beliefs about their body size are accurate and what effect a correct or incorrect assessment of one's body size has in terms of actual behavior. I examine this question among adolescent girls using data from the 2002 Health Behaviors in School-Age Children Survey. With a sample of 2,784 girls between the ages of 11 and 17, I run Poisson regression models to assess the relationship between actual and perceived body size and healthy versus unhealthy weight control behaviors, controlling for a number of indicators known to be associated with weight control, including parent and peer relationships, media exposure, and age of first menstruation. Results indicate that a discrepancy between actual and perceived body size is associated with increases in both positive and negative weight control behaviors, though the association with negative weight control behaviors is much larger. Starting puberty later is associated with a decrease in both types of these behaviors. Difficult family relationships appear to be more strongly associated with negative weight control than positive weight control. Other associations are discussed and suggestions for future research are offered.

Body size is one of the most commonly studied traits of an organism, which is largely due to its direct correlation with fitness, life history strategy, and physiology of the organism. Patterns of body size distribution are also often studied. The distribution of body size within species is looked at for suggestions of differential mating strategies or niche variation among ontogenetic development. Patterns are also examined among species to determine the effects of competition, environmental factors, and phylogenetic inertia. Finally, the distribution of body size across the geographic range of a species or group of closely related is looked at for indications of the effects of climate and resource availability on body size at different latitudes and altitudes. In this collection of research, I address the evolution and importance of body size in burying beetles (genus Nicrophorus). Body size is important to several aspects of burying beetle natural history, including competitive ability, fitness, parental care, climate tolerance, and locomotor activity. In Chapter 1, I use a large data set of body size measurements for seventy of the seventy-three Nicrophorus species to make inferences about the distribution of body size within the genus, across its geographic range, and the importance of body size in speciation. I found that the range of body sizes is not normally distributed, with an overrepresentation of small-sized species. I also found that expansion of the burying beetle range has been restricted by their inability to tolerate warm, dry climates, and therefore the majority of burying beetle diversity occurs in the temperature mid-latitudes of the northern hemisphere. Body size also seems to be important in speciation, as almost all sister taxa are significantly different in body size. In Chapter 2 I use common garden experiments to assess the importance of body size for males and females in competition, reproductive output, and starvation resistance. Body size is equally important for both sexes in starvation resistance, but it is more important for males in competitions for carcasses and for females in reproductive output. In Chapter 3 I test for fitness consequences of multigenerational effects of body size in offspring. I found that the larger offspring that are produced by larger mothers and on larger carcasses had higher fitness than small offspring. In Chapter 4 I test for the possibility of brood parasitism in two species of burying beetles, N. guttula and N. marginatus, which co-occur over part of their geographic ranges. I found that both species are able to detect and remove parasitic larvae. Finally, in Chapter 5 I compiled parent and offspring body sizes from seven species of burying beetles and use them to compare the heritability of body size among species using comparative techniques and a meta-analysis. I found that body size heritability is different between species, but is low for the genus as a whole. Together, these projects provide valuable information on the evolutionary significance of body size in Nicrophorus, and indicate compelling questions for future research into the evolution of body size in burying beetles.

No description available.

Body size is one of the most fundamental quantifiable traits of living or fossil organisms, and understanding it in various temporal and spatial contexts can offer key insights into the process of evolution. This volume examines body size of eukaryotes and its correlates in various temporal and spatial contexts in three distinct studies. The first study investigates the relationship between parasitism and body size of modern bivalve hosts. Individuals of Protothaca staminea were extensively parasitized (86%) by two types of trace-producing parasites. The only significant relationship between parasitism and body size was that spionid mudblister infested clams from one environment were slightly, yet significantly, smaller than their non-infested counterparts. The most obvious pattern regarding body size was that clams from a lagoon were significantly larger than clams from a tidal creek. This size discrepancy could be related to environmental stress, durophagous predators, differing hydrodynamic conditions, or the comparison of differing cohorts. Even though there was no discernible impact of trematode parasitism on bivalve body size, their traces were abundant and easy to identify. Investigators of body size in the fossil record should be aware of these organisms and their possible ramifications for body size studies. The second study, using Quaternary terrestrial gastropods from the Canary Islands, tests the hypothesis of limiting similarity, the idea that two closely related species will alter their size/morphology in order to minimize competition. By integrating amino acid geochronology, stable isotope estimates, and morphometric techniques I was able to more adequately test whether limiting similarity is an evolutionary process or a transient ecological phenomenon. The first prediction of limiting similarity, character displacement, was confirmed. The second prediction of limiting similarity, character release, was not confirmed. It appears that changing climate at the end of the Pleistocene may be responsible for the body size trends, but intraspecific competition likely played a secondary role in the evolution of body size of Theba. The third study addressed the history of body size and morphological disparity of the first 1.3 billion years of acritarch history. The results reject the idea that acritarch body size increased monotonically through the Proterozoic; in fact they displayed non-directional fluctuation. Acritarch body size decreased significantly following the first appearance of Ediacara organisms and gradually rose during the Cambrian. Morphological disparity increased a half billion years before the first taxonomic radiation. Morphological disparity decreased significantly during the snowball earth events and upon the first appearance of Ediacaran organisms suggesting multiple events of selective extinction in the Proterozoic biosphere. Disparity then increased in step with the diversification of acritarch and metazoans through the Cambrian suggesting ecological links between the two groups. Ecological processes, whether extrinsic abiotic processes or biotic interactions, influence the body size and evolution of organisms at wide range of spatial and temporal scales. / Ph. D.

No description available.

Thesis (PhD)--Stellenbosch University, 2013. / ENGLISH ABSTRACT: The challenge of conserving biodiversity is daunting. Despite some local conservation gains, most indicators of the condition of global biodiversity show declines since the 1970’s, while indicators of the threats to biodiversity all show increases. Humanity has in part responded to the global biodiversity extinction crisis by establishing protected areas (PA) and they are widely considered cornerstones of conservation. However, their efficacy in maintaining biodiversity is much debated. Previous studies have been unable to provide a general answer because of their typically restricted geographic and/or taxonomic focus, or qualitative approach. Using a global meta-analysis with 861 pairwise comparisons inside and outside PAs from 86 studies across five major taxon groups, I tested the hypothesis that PAs achieve significant conservation outcomes measured as higher biodiversity values compared with alternative land covers. I found that globally, PAs typically contain higher abundances of individual species, higher assemblage abundances and higher species richness. Variation in effect sizes among taxa nonetheless underscores that PA efficacy can be context specific. To examine factors driving the context specific nature of PA efficacy, an exact distance, timed point count methodology was used to assess PAs ecological effectiveness in terms of bird assemblages of the Kruger National Park (KNP), South Africa, in the Phalaborwa section. Bird assemblages inside the KNP were compared to matched sites in rural and urban land cover, as well as the connecting habitat matrix outside the KNP. Species richness and abundance were significantly lower inside the KNP compared to other land covers. However, the species assemblages are markedly different. The artificial addition of resources in an otherwise resources poor area, mainly in terms of gardening, provide suitable habitat for a range of species, consistent with the more individuals hypothesis. Large-bodied and ground nesting species are virtually absent outside the KNP. Thus species richness and abundance differences between land cover regions mask insidious changes in species traits. Nonetheless, not formally protected land can contribute positively to the regional biodiversity portfolio. Since an understanding of the mechanisms that structure species assemblages can aid in the consequences of anthropogenic drivers disentangling them, I describe and analyse the body size frequency distributions (BSFDs) of avian assemblages at several spatial scales in the Afrotropical biogeographic realm. I found that the African avifaunal continental BSFD is unimodal and right-skewed. African avifaunal BSFDs are quantitatively dissimilar to the African mammal BSFDs, which are bimodal at all spatial scales. Much of the change in median body size with spatial scale can be captured by a range-weighted null model, suggesting that differential turnover between smaller- and larger-bodied species might explain the shift in the central tendency of the BSFD. My results for the first time quantitatively demonstrate that PAs are a vital component of a global biodiversity conservation strategy. However, I also show that PA ecological effectiveness can be context specific, and understanding which species traits are at risk outside of PAs is critical to predicting their efficacy. / AFRIKAANSE OPSOMMING: Dit is ‘n uitnemende uitdaging om biodiversiteit te bewaar. Ten spyte van sommige sukses op ‘n lokale skaal, dui die meeste indikators aan dat die toestand van globale biodiveristeit afgeneem het vanaf die 1970’s, terwyl bedreigings daartoe toegeneem het. Die mensdom het gedeeltelik reageer op die biodiversiteits uitsterfings krisis deur die uiteensetting en instandhouding van bewaringsgebiede (BG). Hierdie metodiek word wêreldwyd geag as ‘n hoeksteen van bewaring. Die ekologiese doeltreffendheid van BG word egter baie debateer. Vorige studies was geografies beperk of het net op sekere takson groepe gefokus. Vorige studies is ook tipies statisties kwalitatief van aard. As gevolg daarvan het ek ‘n globale meta-analiese gebruik, wat bestaan het uit 861 gepaarde meetings vanaf 86 studies, oor vyf verskillende taksonomiese groepe. Ek het die hipotese getoets dat BG statisties beduidende bewaring laat gekiet in terme van hoër biodiveristeits waardes binnekant hul grense, in kontras met areas buite BG. Ek het gevind dat BG juis hoër waardes van hoër indivuduele spesies hoeveelhede, gemeenskaps hoeveelhede en spesiesrykheid bevat. Tog dui die variasie in effek grootte onder takson groepe aan dat BG effektiwiteit konteks spesifiek is. Aangesien BG effektiwiteit konteks spesifiek is, het ek verder ‘n tydstip, eksakte-afstand punttelling metodiek gevolg om die Kruger Nationale Park (KNP) in Suid Afrika, se ekologiese doeltreffendheid te bepaal. Ek het voëlgemeenskappe binne KNP vergelyk met voëlgemeenskappe buite KNP. Metings is buite die KNP gedoen in tuislande, die stadsgebied van Phalaborwa, asook in die habitat matriks wat die areas verbind. Beide spesiesrykheid en hoeveelheid is hoër buite KNP, maar die voëlgemeenskap struktuur tussen gebiede verskil noemenswaardig. Die uitbreiding van bronne ten opstigte van nesmaak en voeding (meestal deur tuinmaak), bied vir voëls goeie habitat in die stadsgebied, soos verwag kan word uit die meer individue hipotese. Hierdie veranderinge in spesiesrykheid tussen die verskillende areas versteek veranderinge in die spesies einskappe. Voëls met groot liggaamsmassa, veral die wat op die grond nes maak, kom in baie minder getalle voor buite KNP. Tog bied onbewaarde areas ‘n positiewe inpak tot die omgewing se biodiversiteit. ‘n Holistiese begrip van die meganismes wat spesies gemeenskappe struktureer kan help om die menslike invloed daarop uit te lig. Daarvolgens beskryf ek die liggaamsmassa frekwensie verspreiding (LMFV) oor verkillende skale in die Afrotropies biografiese streek. Ek het bevind dat Afrika se voëlgemeenskappe op die kontinentale skaal unimodaal en regs-geskewe is. Afrika se voël LMFV is beduidend verskillend van Afrika soogdier LMFV, wat bimodaal is op verskeie skale. Baie van die verandering in mediaan liggaams massa oor verskillende skale kan verduidelik word met ‘n verspreidings-aangepaste nul-model, wat voorstel dat die verskille in omset van voëls met of klein, of groot liggaamsmassa in die landskap die veranderings in LMFV verduidelik. My studie is die eerste van sy soort wat kwantitatief bepaal dat die gebruik van BG krities is tot ‘n globale bewaringsstrategie. Verder het ek bewys dat BG se ekologiese doeltreffendheid afhang van die kontkes op ‘n lokale skaal, en dat spesies eienskappe geïnkorporeer moet word om BG se doeltreffendheid te bepaal.

Monitor lizards (Varanidae) are morphologically very uniform in body shape, but much diversified in body size along both phylogenetic and ontogenetic axes. A striking sexual size dimorphism exists in monitor lizards; they are capable of fast growth, metabolism and sexual maturation. I collected the data concerning body size of particular species and verified the validity of Rench's rule, which said that there is bigger difference in body size of a conspecific male and females growing with larger body size of the species. Males are markedly bigger than females. In the next step, I focused on the model species of monitor lizards, Varanus indicus. I monitored its ontogeny very carefully. I found that this monitor lizard has pronounced sexual size dimorphism, but there are only small differences in body shape. It is capable of rapid growth and sexual maturation. The sexual dimorphism in body shape is only poor, but still measurable right in those places where the selection pressures were expected. Blood sampling monitored biochemical and haematological parameters. The concentrations of the biochemical parameters revealed the economy of resources of particular sexes partially, the costs of body growth and reproduction. Although both sexes produce the same amount of biomass (the body growth of males vs. the...

Body size has a potential to influence almost any trait in animal biology. The thesis contains four case studies (I - IV) covering four various situations and four various taxa, mainly squamate reptiles (Lepidosauria). Body size is a connecting factor for all these studies, in which I and my co-authors tried to elucidate various implications of body size. I. The sex ratio in Cuban boa (Chilabothrus angulifer) litters is often male or female biased. The neonates are so large, that are able to accept the same type of prey as are adults (in contrast to the other Chilabothrus species). We found that both the sexes are of the same size and shape at birth. Large size of the neonates a long lifespan lead to considerable generation overlaps. This could clarify our findings that small females produce sons whereas the larger ones deliver daughters. Males are smaller than females, probably also less philopatric and refuse food during breeding season. We can conclude that females manipulate the sex ratio of neonates according to its own body size, in order to decrease the probability of competition with their own offspring. II. Mangrove-dwelling monitor lizard (Varanus indicus) shows one of the greatest degrees of sexual size dimorphism among monitor lizards. We recorded the growth of the individuals from...

Whether microevolutionary processes can explain macroevolutionary patterns has long been a matter of contentious debate. The debate has persisted largely because of the challenging task of connecting microevolutionary theory, which examines population-level phenomena on the generation scale, to data collected across larger spatial and temporal scales. My dissertation research broadly examines phenotypic evolution across multiple scales by connecting microevolutionary theory to macroevolutionary phenomena such as speciation and large-scale phenotypic change. In particular, I focus on the so-called "paradox of stasis"; which wrestles with the apparent conflict between frequently-observed cases of rapid evolution on short timescales and the frequent appearance of stasis in the fossil record. I attempt to link micro and macroevolution by using the theoretical framework of evolutionary quantitative genetics for modeling the effects of drift and selection. My four dissertation chapters examine four different systems (1) connecting quantitative genetic models of sexual selection to speciation (2) connecting microevolutionary and macroevolutionary body size data across scales of time (3) using phylogenetic comparative methods and quantitative genetic models to examine the evolution of a classic example of stasis, mammalian body temperature and (4) finally, using multi-locus phylogeography to understand the evolutionary processes that contribute to the diversification of a widespread snake across broad spatial scales. In chapter 2, I demonstrate that genetic drift combined with sexual selection can promotes speciation and diversification of male ornaments. Furthermore, I demonstrate that drift promotes the evolution of elaborate ornaments even when preferences are costly. In chapter 3, I combine data from microevolutionary field studies, the fossil record, and phylogenetic comparative data into a single analytical framework to resolve apparent conflicts between micro and macroevolutionary patterns. To do so, I compiled and analyzed the largest database of phenotypic divergence data in existence. I demonstrate that patterns of stasis persist until a million-year threshold, after which divergence begins to accumulate in a time-dependent manner. This pattern is best fit with a hierarchical model that describes evolution as occurring in bursts on the million-year timescale, but that allows for rapid, but bounded, evolution on short timescales. In chapter 4, I demonstrate that mammalian body temperature -- which has been previously presented as a classic example of stasis -- does in fact evolve extensively across the mammalian radiation (albeit slowly). Furthermore, I show that mammalian body temperature evolves in response to changing environmental conditions. Finally, I evaluate the role that genetic constraints play in the apparent slowness of body temperature evolution. In chapter 5, I examine a well-studied empirical system of garter snakes in which a strong signature of stabilizing selection has been found for phenotypic traits. Using multiple mitochondrial and nuclear loci, I show that introgression is rampant between species, and dynamic patterns of range expansion, contraction, and introgression among clades have led to a complex pattern of genetic variation. This structure of genetic variation underscores the need to examine range-wide processes for generating phenotypic divergence across clades. Overall, these chapters suggest that apparent disconnects between microevolutionary processes and macroevolutionary patterns could be explained by the scaling of population-level theory over large spatial and temporal scales. / Graduation date: 2013 / Access restricted to the OSU Community at author's request from Oct. 25, 2012 - Oct. 25, 2013