The anatomy of the interspecific abundance–range size relationship for the British avifauna: I. Spatial patterns

Data from the British Trust for Ornithology Common Birds Census and two atlases of breeding birds were used to examine the form of the interspecific abundance–range size relationship for the British avifauna. The relationship is positive for both farmland and woodland habitats and over two different periods, with some evidence of curvilinearity, using either proportion of occupied sites or numbers of occupied 10 × 10 km squares as measures of range size, and mean density at occupied sites as a measure of abundance. A log-linear plot gives the highest correlation. The relationship is stronger if based on maximum local densities than if based on average densities, but there is no relationship using minimum local densities. Relationships based on abundances at individual sites are uniformly positive for all sites, although the relationships for many sites also show evidence of curvilinearity, especially when range size is measured as the proportion of occupied sites. Species show significant concordance in their rank abundances across sites. We discuss some implications of these results.     

The anatomy of the interspecific abundance–range size relationship for the British avifauna: II. Temporal dynamics

In a companion paper, we started an examination of the anatomy of the interspecific relationship between local abundance and geographical range size in the British avifauna by analysing its spatial dynamics. Here, we use the same data to extend this study to a consideration of the temporal dynamics of the relationship. Most species of British breeding bird show a positive intraspecific abundance–range size relationship through time: i.e. in years when a species is locally more abundant it also occupies a higher proportion of census sites. However, the majority of such relationships are not statistically significant, and other relationships that are statistically significant are negative. Therefore, intraspecific abundance–range size relationships do not simply mirror the relationship across species. Where they do arise, positive relationships are more likely to be associated with positive intraspecific relationships between range size and maximum rather than minimum abundance. The interspecific abundance–range size relationship is remarkably consistent across years, and is always significantly positive. The relationships for woodland and farmland census sites show correlated variation, so that in years when the linear regression slope and coefficient of determination are high across species on farmland plots, they also tend to be high across species on woodland plots. Common species tend to be common on both farmland and woodland plots, and tend to be common in all years. Likewise, rare species tend to be rare in all habitats and years. This concordance means that the positive interspecific abundance–range size relationship can be viewed as occurring largely independently of intraspecific relationships. It follows from the above that developing an understanding of intraspecific abundance–range size relationships may be of only limited value in ascertaining the determinants of positive interspecific abundance–range size relationships. We conclude that for interspecific relationships, it will be important to know why some species are consistently common and others rare, whereas for intraspecific relationships it will be important to understand the dynamic links between local abundances across sites.     

Variations on a theme: sources of heterogeneity in the form of the interspecific relationship between abundance and distribution

1. A positive interspecific relationship between abundance and distribution is widely considered to be one of the most general patterns in ecology. However, the relationship appears to vary considerably across assemblages, from significant positive to significant negative correlations and all shades in between. 2. This variation has led to the suggestion that the abundance-distribution relationship has multiple forms, with the corollary that different patterns may inform about, or have different, causes. However, this variation has never been formally quantified, nor has it been determined whether the observed variation is indicative of sampling error in estimating a single effect or of real heterogeneity in such relationships. Here, we use the meta-analytical approach to assess variation in abundance-distribution relationships, and to test different hypotheses for it. 3. Analysis of 279 relationships found a mean effect size of 0.655, which was both highly significantly different from zero and indicative of a strong positive association between abundance and distribution. However, effect sizes were highly heterogeneous, supporting the contention that this relationship does indeed have multiple forms. 4. Most notably, relationships vary significantly in strength across realms, with the strongest in the marine and intertidal, intermediate relationships for terrestrial and parasitic assemblages, and the weakest relationships in freshwater systems. Effect sizes in all of the aquatic realms are homogeneous, suggesting that realm is an important source of the heterogeneity observed across all studies. We posit that this may be because the different spatial structure of the environment in each realm affects the opportunity for the dispersal of individuals between sites. 5. Some of the remaining heterogeneity in effect sizes for terrestrial assemblages could be explained by partitioning assemblages by habitat, scale, biogeographical region and taxon, but considerable heterogeneity in effect sizes for terrestrial and parasitic assemblages remained unexplained.     

The comparative ecology and biogeography of parasites

Comparative ecology uses interspecific relationships among traits, while accounting for the phylogenetic non-independence of species, to uncover general evolutionary processes. Applied to biogeographic questions, it can be a powerful tool to explain the spatial distribution of organisms. Here, we review how comparative methods can elucidate biogeographic patterns and processes, using analyses of distributional data on parasites (fleas and helminths) as case studies. Methods exist to detect phylogenetic signals, i.e. the degree of phylogenetic dependence of a given character, and either to control for these signals in statistical analyses of interspecific data, or to measure their contribution to variance. Parasite–host interactions present a special case, as a given trait may be a parasite trait, a host trait or a property of the coevolved association rather than of one participant only. For some analyses, it is therefore necessary to correct simultaneously for both parasite phylogeny and host phylogeny, or to evaluate which has the greatest influence on trait expression. Using comparative approaches, we show that two fundamental properties of parasites, their niche breadth, i.e. host specificity, and the nature of their life cycle, can explain interspecific and latitudinal variation in the sizes of their geographical ranges, or rates of distance decay in the similarity of parasite communities. These findings illustrate the ways in which phylogenetically based comparative methods can contribute to biogeographic research.     

High proportion of smaller ranged hummingbird species coincides with ecological specialization across the Americas

Ecological communities that experience stable climate conditions have been speculated to preserve more specialized interspecific associations and have higher proportions of smaller ranged species (SRS). Thus, areas with disproportionally large numbers of SRS are expected to coincide geographically with a high degree of community-level ecological specialization, but this suggestion remains poorly supported with empirical evidence. Here, we analysed data for hummingbird resource specialization, range size, contemporary climate, and Late Quaternary climate stability for 46 hummingbird–plant mutualistic networks distributed across the Americas, representing 130 hummingbird species (ca 40% of all hummingbird species). We demonstrate a positive relationship between the proportion of SRS of hummingbirds and community-level specialization, i.e. the division of the floral niche among coexisting hummingbird species. This relationship remained strong even when accounting for climate, furthermore, the effect of SRS on specialization was far stronger than the effect of specialization on SRS, suggesting that climate largely influences specialization through species'' range-size dynamics. Irrespective of the exact mechanism involved, our results indicate that communities consisting of higher proportions of SRS may be vulnerable to disturbance not only because of their small geographical ranges, but also because of their high degree of specialization.     

Correlates of sexual dimorphism in primates: Ecological and size variables

The effects of a series of ecological and size factors on the degree of sexual dimorphism in body weight and canine size were studied among subsets of 70 primate species. Variation in body-weight dimorphism can be almost entirely attributed to body weight (83% of variance R² of weight dimorphism). Much smaller amounts of the variation can be attributed to mating system (R² =6.8%,polygynous species being more dimorphic than monogamous ones) and diet (R² = 2.5%,frugivorous species being more dimorphic than folivorous ones). Habitat (arboreal vs. terrestrial) and activity rhythm (nocturnal vs. diurnal) have only an indirect effect on weight dimorphism. Variation in canine-size dimorphism can be explained in terms of canine size (R² =49%),activity rhythm (R² = 20%,diurnal species being more dimorphic than nocturnal ones), and mating system (R² = 10%).Habitat and diet do not play a significant role in canine-size dimorphism. The unexpectedly high contribution of size to sexual dimorphism coupled with the observation of increased sexual dimorphism with increased size leads us to formulate a new selection model for the evolution of sexual dimorphism. We suggest that if there is selection for size increase, whatever its cause, directional selection in both males and females will lead to an increase in sexual dimorphism based on differences in genetic variance between the sexes. Sexual selection, resource division between the sexes, or lopsided reproductive selection need not play a role in such a model.     

The evolution of the social brain: anthropoid primates contrast with other vertebrates

The social brain hypothesis argues that large brains have arisen over evolutionary time as a response to the social and ecological conflicts inherent in group living. We test predictions arising from the hypothesis using comparative data from birds and four mammalian orders (Carnivora, Artiodactyla, Chiroptera and Primates) and show that, across all non-primate taxa, relative brain size is principally related to pairbonding, but with enduring stable relationships in primates. We argue that this reflects the cognitive demands of the behavioural coordination and synchrony that is necessary to maintain stable pairbonded relationships. However, primates differ from the other taxa in that they also exhibit a strong effect of group size on brain size. We use data from two behavioural indices of social intensity (enduring bonds between group members and time devoted to social activities) to show that primate relationships differ significantly from those of other taxa. We suggest that, among vertebrates in general, pairbonding represents a qualitative shift from loose aggregations of individuals to complex negotiated relationships, and that these bonded relationships have been generalized to all social partners in only a few taxa (such as anthropoid primates).     

Further perspectives on the breeding distribution of migratory birds: South American austral migrant flycatchers

1. Patterns of distribution of breeding austral migrant tyrant-flycatchers in temperate South America were quantified and analysed in conjunction with a variety of ecological, biogeographical and climatic variables.
2. The pattern of proportion of migratory to total breeding tyrannids was most strongly associated with latitude and two temperature variables, mean temperature of the coldest month and relative annual range of temperature.
3. The strong associations of latitude and temperature with percentage of migrants are consistent with the results of most similar investigations of the breeding distributions of migratory birds, both for migrants breeding in North America and in Europe, but contradict the hypothesis that habitat complexity plays a major role in structuring the proportion of migrants in communities of breeding birds.
4. The consistency of results among studies of migrants on different continents suggests that temperature and latitude, presumably a surrogate for one or more climatic variables, are globally significant factors in the breeding distributions of migratory birds.
5. The results for austral migrant flycatchers are consistent with the hypothesis that the prevalence of migration at any particular locality is ultimately dependent on the abundance of resources in the breeding season and the severity of the winter season, or on the difference in resource levels between summer and winter.     

More and more generalists: two decades of changes in the European avifauna

Biotic homogenization (BH) is a process whereby some species (losers) are systematically replaced by others (winners). While this process has been related to the effects of anthropogenic activities, whether and how BH is occurring across regions and the role of native species as a driver of BH has hardly been investigated. Here, we examine the trend in the community specialization index (CSI) for 234 native species of breeding birds at 10 111 sites in six European countries from 1990 to 2008. Unlike many BH studies, CSI uses abundance information to estimate the balance between generalist and specialist species in local assemblages. We show that bird communities are more and more composed of native generalist species across regions, revealing a strong, ongoing BH process. Our result suggests a rapid and non-random change in community composition at a continental scale is occurring, most likely driven by anthropogenic activities.