Body size and abundance relationship: an index of diversity for herbivores

It is evident to any biologist that small-bodied species within a given higher taxon (order, class, phylum, etc.) tend to be represented by more individuals. Hence small-bodied species are generally more abundant than large-bodied species. We analyzed large herbivore species data collected in Kenyan rangelands. An index of biological diversity derived from the negative relation between animal species body size and its local abundance is proposed. We compared the new index with species abundances at landscape scale (10 × 10 km) in individual districts, as well as in the combined regional data. The results show a consistently strong positive relation between the new diversity index and species abundances. The proposed diversity index has the advantage of incorporating information on species abundances without the need for time-consuming surveys.     

Body size frequency distributions in African mammals are bimodal at all spatial scales

Aim  To examine frequency distributions of body sizes for mammal assemblages at several spatial scales and assess the generality of results heretofore obtained only for North and South America.
Location  Africa.
Methods  Terrestrial African mammals were allocated to major biomes, and regional and local assemblages were extracted from published and unpublished literature. We produced body size frequency distributions for local, regional, biomic and continental distributions, both for whole assemblages and for three foraging strata, and compared these with several standard metrics (e.g. mean and median size, interquartile range, skew, bimodality, etc.). Differences between distributions were quantified using t -tests and analysis of variance.
Results  African mammal faunas exhibit features in common with those of North and South America, most notably the gradual reduction in the modality and skew of body size distributions with decreasing spatial scale. Unlike other continents, however, the African mammal fauna exhibits a bimodal frequency distributions at all spatial scales. Our data suggest a role for competitive interactions in local assembly, as documented elsewhere, but further data on locally interacting assemblages are needed.
Main conclusions  The African fauna appears unique in the expression of bimodality at all spatial scales. The presence of a secondary mode at large body size may reflect co-evolutionary adjustments to proto-human hunters and consequent escape from anthropogenic Pleistocene extinctions, but the absence of species of intermediate body size ( c . 250–4000 g) remains anomalous and is not readily explained by either historical or modern (ecological) factors. For the African mammal fauna, a key question in understanding the role of history versus ecology may not be why there are so many large species, but why there are so few intermediate-sized species.     

Patterns of maximum body size evolution in Cenozoic land mammals: eco-evolutionary processes and abiotic forcing

There is accumulating evidence that macroevolutionary patterns of mammal evolution during the Cenozoic follow similar trajectories on different continents. This would suggest that such patterns are strongly determined by global abiotic factors, such as climate, or by basic eco-evolutionary processes such as filling of niches by specialization. The similarity of pattern would be expected to extend to the history of individual clades. Here, we investigate the temporal distribution of maximum size observed within individual orders globally and on separate continents. While the maximum size of individual orders of large land mammals show differences and comprise several families, the times at which orders reach their maximum size over time show strong congruence, peaking in the Middle Eocene, the Oligocene and the Plio-Pleistocene. The Eocene peak occurs when global temperature and land mammal diversity are high and is best explained as a result of niche expansion rather than abiotic forcing. Since the Eocene, there is a significant correlation between maximum size frequency and global temperature proxy. The Oligocene peak is not statistically significant and may in part be due to sampling issues. The peak in the Plio-Pleistocene occurs when global temperature and land mammal diversity are low, it is statistically the most robust one and it is best explained by global cooling. We conclude that the macroevolutionary patterns observed are a result of the interplay between eco-evolutionary processes and abiotic forcing.     

Phylogenetic diversity does not capture body size variation at risk in the world's mammals

Mammals contribute to important ecosystem processes and services, but many mammalian species are threatened with extinction. We compare how global patterns in three measures of mammalian diversity—species richness, phylogenetic diversity (PD) and body mass variance (BMV)—would change if all currently threatened species were lost. Given that many facets of species'' ecology and life history scale predictably with body mass, the BMV in a region roughly reflects the diversity of species'' roles within ecosystems and so is a simple proxy for functional diversity (FD). PD is also often considered to be a proxy for FD, but our results suggest that BMV losses within ecoregions would be much more severe than losses of PD or species richness, and that its congruence with the latter two measures is low. Because of the disproportionate loss of large mammals, 65 per cent of ecoregions would lose significantly more BMV than under random extinction, while only 11 per cent would lose significantly more PD. Ecosystem consequences of these selective losses may be profound, especially throughout the tropics, but are not captured by PD. This low surrogacy stresses a need for conservation prioritization based on threatened trait diversity, and for conservation efforts to take an ecosystem perspective.     

Sperm competition and brain size evolution in mammals

The ‘expensive tissue hypothesis’ predicts a size trade‐off between the brain and other energetically costly organs. A specific version of this hypothesis, the ‘expensive sexual tissue hypothesis’, argues that selection for larger testes under sperm competition constrains brain size evolution. We show here that there is no general evolutionary trade‐off between brain and testis mass in mammals. The predicted negative relationship between these traits is not found for rodents, ungulates, primates, carnivores, or across combined mammalian orders, and neither does total brain mass vary according to the level of sperm competition as determined by mating system classifications. Although we are able to confirm previous reports of a negative relationship between brain and testis mass in echolocating bats, our results suggest that mating system may be a better predictor of brain size in this group. We conclude that the expensive sexual tissue hypothesis accounts for little or none of the variance in brain size in mammals, and suggest that a broader framework is required to understand the costs of brain size evolution and how these are met.     

Variability and size in mammals and birds

Body size, its variability, and their ecological correlates have long been important topics in evolutionary biology. Yet, the question of whether there is a general relationship between size and size-relative variability has not previously been addressed. Through an analysis of body-mass and length measurements from 65 074 individuals from 351 mammalian species, we show that size-relative variability increases significantly with mean species body size. Analysis of mean body mass and standard deviations for 237 species of birds revealed the same pattern. We present three plausible alternatives explanations and eliminate several others. Of these, the hypothesis that the increase in size-relative variability with mean body mass is related to the scaling of body mass components is most strongly supported. In effect, larger mammals and birds are more variable because their body mass is composed to greater relative degree of components with higher intrinsic variability (bone, fat, and muscle). In contrast, smaller mammals and birds have lower body mass variability because they are composed to a greater relative extent of components (viscera and nervous system) in which size variation is more highly constrained by energetic and functional factors.     

Body size in (mostly) mammals: mass,speciation rates and the translation of gamma to alpha diversity on evolutionary timescales

This study tests the hypothesis that high species richness in small-bodied mammals results from higher speciation rates than in clades composed of large-bodied individuals. A right-skewed pattern is evident in size distributions of all mammal groups tested. Gaps between 100 g bins expand smoothly for the global mammal database. Less diverse mammal clades composed of large-sized individuals originated at relatively large size. Mechanisms promoting isolation and higher speciation rates in small mammals include the environmental mosaic, low absolute energy needs, small home range size, stenotopy, and intraspecific competition. A decline in diversity for the smallest size category in some clades suggests there is a lower limit in homoiotherms of about 1.5–2 g, possibly related to high metabolic rate and high surface area to volume ratio. Mammal size diversity from young Canadian ecosystems (≤19,000 years BP) is right-skewed, and diversity of species per unit area is approximately the same as for North America. Diversity and size distributions for mammals and select animal groups from southern Minnesota follow expected right-skewed patterns, suggesting the inverse relationship of body size and speciation rate is universal for complex metazoans. A logistic model is presented integrating γ and α diversity over evolutionary timescales.     

The evolution of body armor in mammals: plantigrade constraints of large body size

Predictions associated with opposing selection generating minimum variance in basal metabolic rate (BMR) in mammals at a constrained body mass (CBM; 358 g) were tested. The CBM is presumed to be associated with energetic constraints linked to predation and variable resources at intermediate sizes on a logarithmic mass scale. Opposing selection is thought to occur in response to energetic constraints associated with predation and unpredictable resources. As body size approaches and exceeds the CBM, mammals face increasing risks of predation and daily energy requirements. Fast running speeds may require high BMRs, but unpredictable and low resources may select for low BMRs, which also reduce foraging time and distances and thus predation risks. If these two selection forces oppose each other persistently, minimum BMR variance may result. However, extreme BMR outliers at and close to the CBM should be indicative of unbalanced selection and predator avoidance alternatives (escapers vs. defenders), and may therefore provide indirect support for opposing selection. It was confirmed that body armor in defenders evolves at and above the CBM, and armored mammals had significantly lower BMRs than their nonarmored counterparts. However, analyses comparing the BMR of escapers--the fastest nonarmored runners (Lagomorpha)--with similar-sized counterparts were inconclusive and were confounded by limb morphology associated with speed optimization. These analyses suggest that the risks and costs of predation and the speed limitations of the plantigrade foot may constrain the evolution of large body sizes in plantigrade mammals.     

Genome size variation and species diversity in salamanders

Salamanders (Urodela) have among the largest vertebrate genomes, ranging in size from 10 to 120 pg. Although changes in genome size often occur randomly and in the absence of selection pressure, nonrandom patterns of genome size variation are evident among specific vertebrate lineages. Several reports suggest a relationship between species richness and genome size, but the exact nature of that relationship remains unclear both within and across different taxonomic groups. Here, we report (a) a negative relationship between haploid genome size (C‐value) and species richness at the family taxonomic level in salamander clades; (b) a correlation of C‐value and species richness with clade crown age but not with diversification rates; (c) strong associations between C‐value and both geographic area and climatic‐niche rate. Finally, we report a relationship between C‐value diversity and species diversity at both the family‐ and genus‐level clades in urodeles.     

Home range, home range overlap, and species energy use among herbivorous mammals

Harestad & Bunnell (1979) showed that, at least for North American species, home ranges of large herbivorous mammals are relatively larger than we would expect on metabolic grounds, and suggested that the productivity of the environment for mammal species decreases with increasing body size. This interpretation assumes that the number of conspecifics that share an individual's home range is independent of body size. Data presented here show that this is not true for the species in their sample; the home range is shared with an increasing number of conspecifics in larger herbivore species. The productivity of the environment for a species is independent of body size and the area available to an individual for its own use scales approximately as do individual metabolic requirements. These results agree with conclusions based upon the scaling of population density with body mass and illustrate the interrelationship between home range and dietary and social organization trends among mammalian herbivores. Individual home range area is a function of the way in which the local population of a species, not merely an individual, exploits the environment.     

放牧压力条件下荒漠草原小型哺乳动物群落多样性的空间格局

在植物生长期 ,采用夹日法对放牧扰动下的祁连山北坡山地荒漠草地小型哺乳动物群落多样性空间分布格局进行测度 ,结果表明 :在不同的放牧强度条件下 ,小型哺乳动物群落物种组成、结构和多样性指数受相应影响 ,物种丰富度和多样性指数随放牧压力增加而减小 ,经 Whittaker的相似性指数的聚类分析 ,在相似性指数大于 0 .4的水平上 ,可把研究区小型哺乳动物群落分为被家畜啃食和未被家畜啃食 2个类群。研究结果进一步验证了大型食草动物放牧干扰对改变小型哺乳动物群落结构具有重要作用的假设     

Heterothermy,body size,and locomotion as ecological predictors of migration in mammals

1. Migration is ubiquitous among animals and has evolved repeatedly and independently. Comparative studies of the evolutionary origins of migration in birds are widespread, but are lacking in mammals. Mammalian species have greater variation in functional traits that may be relevant for migration. Interspecific variation in migration behaviour is often attributed to mode of locomotion (i.e. running, swimming, and flying) and body size, but traits associated with the evolutionary precursor hypothesis, including geographic distribution, habitat, and diet, could also be important predictors of migration in mammals. Furthermore, mammals vary in thermoregulatory strategies and include many heterothermic species, providing an alternative strategy to avoid seasonal resource depletion.
2. We tested the evolutionary precursor hypothesis for the evolution of migration in mammals and tested predictions linking migration to locomotion, body size, geographic distribution, habitat, diet, and thermoregulation. We compiled a dataset of 722 species from 27 mammalian orders and conducted a series of analyses using phylogenetically informed models.
3. Swimming and flying mammals were more likely to migrate than running mammals, and larger species were more likely to migrate than smaller ones. However, heterothermy was common among small running mammals that were unlikely to migrate. High-latitude swimming and flying mammals were more likely to migrate than high-latitude running mammals (where heterothermy was common), and most migratory running mammals were herbivorous. Running mammals and frugivorous bats with high thermoregulatory scope (greater capacity for heterothermy) were less likely to migrate, while insectivorous bats with high thermoregulatory scope were more likely to migrate.
4. Our results indicate a broad range of factors that influence migration, depending on locomotion, body size, and thermoregulation. Our analysis of migration in mammals provided insight into some of the general rules of migration, and we highlight opportunities for future investigations of exceptions to these rules, ultimately leading to a comprehensive understanding of the evolution of migration.

     

Measuring species diversity while counting large mammals: comparison of methods using species-accumulation curves

With a growing need for wildlife conservation and management in the communal lands of Africa, comprehensive ecological monitoring tools need to be developed and evaluated. While wildlife census methods are often compared in terms of precision and accuracy to estimate the population size of various target species, little attention has been paid to the measure of species diversity in mammal communities. A combined measure of abundance and community composition is, however, a crucial source of information in determining conservation priorities and to evaluate the ecosystem responses to management activities. In this study, we present five census methods of large to medium‐sized mammals and compare their efficacy in measuring species diversity. A species accumulation curve analysis is used with a predictive model to estimate the local species richness, the level of completeness of our censuses as well as the effort required to carry out a census. Advantages and limits of each method are discussed through comparison of their respective measure of species richness and their species accumulation rate. Results illustrate a large difference between methods in the ability for species detection, with censuses completed by bicycle offering the best option within the context of a unprotected area.     

Body size and sexual size dimorphism in calanoid copepods

Patterns of sexual size dimorphism and body size in calanoid copepods are examined. We hypothesize that favorable conditions for development will result in large body size and high sexual size dimorphism among populations of a given species and that differences in this allometric relationship among species is governed by the male's role in insemination. We confirm that there is a greater advantage to large female size, normally the larger sex, when compared to males, hence leading to selection for developmental patterns favoring high size dimorphism. Individuals from populations of four centropagid copepod species were measured; other sizes were obtained from published sources. In the four species we examined, the relationships between prosome length and both clutch size and the ability to produce multiple clutches with one insemination were determined. Results show a trend toward hyperallometry in all centropagid species examined: sexual size dimorphism increases with increasing size. Large females produce larger clutches and more additional clutches on one insemination. That hyperallometry is not observed in diaptomid copepods may result from the greater role the male plays in reproduction. Males are needed for each clutch produced, hence the selective pressure to be larger is greater than that in the centropagidae.     

大中型兽类种群数量估算的研究进展

大中型兽类种群数量的估算是动物生态学中重要的基本问题, 受到研究者、管理者和公众的共同关注。国际上从20世纪中期开始研究该问题, 已出现了多种研究方法和相应案例, 且还在快速发展, 但世界各地仍有很多物种的种群数量尚未知晓。在我国, 从20世纪80年代开始调查大中型兽类种群数量, 取得了重要进展, 也还有很多物种的种群数量尚不清楚。因此, 有必要归纳国际上种群数量估算的研究进展, 同时, 总结国内研究的现状、优势和趋势, 供研究者参考。本文首先选择估算大中型兽类种群数量的原理、数据来源和模型这3个要素归纳出简明的研究框架, 将现有的多种方法置于其中予以阐述。在该框架下, 根据估算原理分为4大类方法, 为距离取样法、标志重捕法、基于遇见率法和遥感影像直接计数法。针对每一大类方法, 论述其基本原理模型和模型假设, 说明能实现该原理的相应数据来源(视觉观测、红外相机拍摄、DNA微卫星识别、卫星定位跟踪、声音监测或遥感影像)的特点及如何实现该原理, 评价其适用性及优缺点, 并选择其中具有可比性的方法予以比较评价。其次, 参照该研究框架, 总结我国的研究现状, 分析未来发展的优势和趋势: 我国的红外相机数据积累充分, 可以发展以此为数据源的距离取样法、标志重捕法和基于遇见率法; 发展以粪便样品为数据来源的距离取样法和粪便DNA标志重捕法; 相比地面调查数据, 获取高分辨率遥感影像数据更容易, 尽量以此估算符合适用条件的大中型兽类的种群数量。最后, 本文提出了适用于我国大中型兽类种群数量的估算方法的选择流程, 供研究者参考。     

绿化植物的生活型对边坡植被物种多样性及护坡性能的影响

为了探讨绿化植物生活型构成对边坡植被物种多样性及护坡性能的影响, 揭示生活型构成-群落特征-物种多样性-生态系统功能间的内在联系, 借助三物种组装实验, 分别构建以草本、灌木或乔木为主体的草本型(HHX_i)、灌木型(SSX_i)、乔木型(AAX_i)或草-灌-乔混合型(HSA)配置模式的实验小区, 对实验区内边坡植被的群落特征、护坡性能进行持续4年的生态监测。结果表明: (1)边坡植被的物种丰富度与绿化植物生活型构成有关, AAX_i的物种丰富度总体高于其他模式, 呈AAX_i > SSX_i > HSA > HHX_i趋势。(2)不同配置模式边坡植被的群落盖度不一样, 年际间差异显著: 建坪初期(2010-2011年), HHX_i的群落盖度远高于其他模式, HSA次之, AAX_i最低; 2012-2013年间, HSA的群落盖度最高, HHX_i次之, AAX_i最低。(3)边坡植被的Shannon-Wiener指数、Pielou指数与绿化植物生活型构成有关, 其变化规律与群落盖度类似: 建坪初期, HHX_i的多样性水平远高于其他模式, 呈HHX_i > HSA > SSX_i > AAX_i趋势; 之后, 呈HSA > HHX_i > SSX_i > AAX_i趋势。(4)边坡植被的护坡性能与群落内的物种多样性密切相关: 多样性水平越高, 护坡性能越强。可见, 在生态护坡过程中, 绿化植物生活型构成对提高边坡植被物种多样性、改善护坡性能至关重要。