The distribution of mammal body masses

How the diversity of organisms relates to their body sizes has long been a question of interest to biologists, an interest that has grown as data have become available from an increasing number of taxa at ever larger spatial scales. Here, we examine the form of this relationship for a large proportion of the global placental mammal fauna. In common with other large-scale assemblages, the frequency distribution of mammal body masses is strongly right-skewed, even after logarithmic transformation. The modal body mass is slightly lower than predicted by a recent energetic fitness model, but the exact modal value depends on the taxonomic inclusivity of the analyses. Moreover, threatened species are larger bodied than expected by chance, suggesting that extinct species may also have been so. Therefore, the loss of large-bodied species from the global mammalian fauna could potentially have lowered the mode of the distribution. However, this loss must be balanced against evidence that most mammal species for which body mass data were not available for our analyses are small-bodied, which may in turn raise the apparent mode of the distribution. Clearly, tests of explanations for patterns in body size frequency distributions will be complicated by the fact that present-day distributions may be significantly biased by species that are missing from them.     

Relationships between abundance and body size: where do tourists fit?

Abstract.

• 1 The possible effects of the inclusion of ‘tourist’ species have been the cause of some concern in investigations of interspecific relationships between abundance and body size.
• 2 Data for adult beetles (Coleoptera) from oak trees in Britain are used to investigate the relationship of abundance to body size when tourists are and are not included.
• 3 For this particular assemblage, tourists do not fundamentally alter the basic statistics of the relationship between abundance and body size. However, they are not a random sample of the beetle assemblage. They have lower abundances and are also of smaller body size than other species.

     

Changes in feeding habit as caterpillars grow

Abstract.

• 1 200 of 1137 species of British microlepidoptera make a single marked change in feeding habit as they grow.
• 2 Most numerous are species that change from leaf mining to one of case bearing, spinning, tying and rolling or concealed feeding, and species that change from concealed feeding to case bearing or spinning, tying and rolling.
• 3 Although in some instances numbers of closely related species make similar changes in behaviour, most changes observed are scattered among subfamilies.
• 4 Leaf miners have considerably smaller adults than concealed feeders, which themselves are smaller than external feeders and spinners, tiers and rollers. When case bearers are excluded from the analyses, species that remain as leaf miners or concealed feeders throughout larval development are on average smaller as adults than those that start out with these feeding habits but later change.
• 5 We suggest a number of reasons why larvae might make such fundamental switches.

     

Living on the edge: British and Irish woodland birds in a European context

This paper reviews broad geographical patterns in the species composition of breeding woodland bird communities from Ireland to eastern Europe and outlines how processes affecting woodland birds in Britain and Ireland may differ from those operating in mainland Europe. Bird communities in British and Irish woodlands consist of a subset of the species occurring within European forests at similar latitudes. The occurrence of virtually all groups of forest birds is lower in Britain, and strikingly lower in Ireland, than in other temperate areas of mainland Europe. This phenomenon appears to form part of a west–east gradient in species diversity and is probably not just a consequence of insularity. Across this gradient there appears to be broad geographical constancy in the types (taxonomic, ecological and life-history groups) of species present. There is considerable spatial variation in habitat use by forest species within Europe. Some species in Britain probably use habitats in different ways to elsewhere for reasons related to competition, predation and historical adaptation to landscape change. Several species appear to reach the limits of their geographical ranges within Britain (i.e. in the absence of physical barriers). We suggest that range contraction of one of these species, the Common Nightingale Luscinia megarhynchos , in Britain may partially reflect redistribution into the highest quality areas in response to a wider population decline. It is argued that conclusions drawn from studies of forest birds in Britain do not necessarily apply in other regions and vice versa. There is a need for large-scale studies in Europe of the spatial variation in organization of forest bird assemblages, habitat use and the genetic structure of populations.     

Patterns in the geographic ranges of the world's woodpeckers

We used data on the world's woodpeckers to test for patterns in the geographic distributions of a single group of closely related species. The frequency distribution of woodpecker geographic range sizes is approximately lognormal. Most variation in range sizes is explained by differences between species within genera; that is, range size seems to be an evolutionarily labile trait. The largest woodpecker ranges are found in Eurasia, both when absolute differences are compared and when range size is measured as a proportion of estimated available habitat. Notably, there is a negative relationship between the mean range sizes attained by species in a genus or tribe in South America and the mean ranges attained by species in the same tribe or genus in North America. Large-bodied species tend to be more widely distributed and to live at higher latitudes, but both tendencies disappear if the taxonomic relatedness of species is controlled for. Species living at high latitudes also tend to be more widely distributed. This relationship seems largely due to the effect of North American woodpeckers, which show it even when the taxonomic relatedness of species is controlled. Small continents generally have more woodpecker species than do large ones. Woodpecker geographic range sizes are smaller the more woodpecker species inhabit an area. Species show less overlap in their geographic ranges with species of similar than with species of dissimilar body size. The implications of these results for our understanding of patterns in geographic range sizes are discussed.