Body size and species richness

Small organisms generally have shorter generation times and are quick to mature and reproduce (May, 1978;[2] Denney et al. 2002;[10] Savage et al. 2004[11]). These traits may promote speciation through increased mutation and selection events as molecular evolution scales with metabolic rate (Gillooly et al. 2005[12]) and thus with body size. For example, bacteria can evolve a degree of antibiotic resistance in a very short time period. This evolution is facilitated by a short generation time and presumably would not be possible for species with slower life histories. Thus, one can think of it as if the "evolutionary clock ticks faster" (May, 1978[2]) for small organisms. If this were true then a simple explanation of why there are more small species on earth would be because they speciate faster. However, a recent analysis by Cardillo and colleagues (2003)[13] revealed that body size did not influence the speciation rates of Australia's mammals. Similarly, a study using birds failed to demonstrate that body size and speciation rates were negatively correlated (Nee et al. 1992[14]).

It is known that extinction risk is directly correlated to the size of a species population. Small populations tend to go extinct more frequently than large ones (MacArthur and Wilson, 1967[15]). As large species require more daily resources they are forced to have low population densities, thereby lowering the size of the population in a given area and allowing each individual to have access to enough resources to survive. In order to increase the population size and avoid extinction, large organisms are constrained to have large ranges (see Range (biology)). Thus, the extinction of large species with small ranges becomes inevitable (MacArthur and Wilson, 1967;[15] Brown and Maurer, 1989;[5] Brown and Nicoletto, 1991[3]). This results in the amount of space limiting the overall number of large animals that can be present on a continent, while range size (and risk of extinction) prevents large animals from inhabiting only a small area. These constraints undoubtedly have implications for the species richness patterns for both large and small-bodied organisms, however the specifics have yet to be elucidated.

Understanding dispersal is an important mechanism that may underlie the body size-species richness pattern. Mainly, dispersal ability can affect speciation rates in various ways: if an organism is capable of dispersing across great distances which span variable habitat, it will be more likely that individuals that settle in these new areas will be subject to different selection regimes, leading to new species through natural selection. Alternatively, great dispersal ability can act against the efforts of natural selection by facilitating geneflow. Thus, species with greater dispersal ability may in fact have lower speciation rates. Then again, if a species disperses long distances and has a large range, it may also be more likely to have its range bisected by natural barriers which could promote allopatric speciation over evolutionary time.

Researchers have shown that body size and dispersal ability do not correlate (Jenkins et al. 2007[16]). However, this finding rests heavily on the fact that active and passive dispersers have been grouped together in the analyses. When the same data are separated into two categories (active and passive dispersers) a pattern emerges. Jenkins and others (2007[16]) have found that for active dispersers larger organisms will disperse greater distances. Regardless of this correlation its effects on speciation rates remain unclear.

Could similar sized species be mitigating the effects of competition by avoiding each other? Interspecific competition is in fact strong among species that are the same size (Bowers and Brown, 1982[17]). Researchers have proposed that in order to lessen the burden of competition among animals within the same guild (see Guild (ecology)), they must vary in size (Brown and Maurer, 1989;[5] Brown and Nicoletto, 1991[3]). For example, Bowers and Brown (1982)[17] found that the number of similar sized species in a community of granivorous rodents was fewer than expected. They believe that these results suggest that competition between same-sized species is prohibiting co-existence in this community.

A small bodied animal has a greater capacity to be more abundant than a large bodied one. Purely as a function of geometry many more small things can be packed into a given space than can large things into the same area. However, these limits are generally never reached in ecological systems as other resources become limiting long before the packing limits are reached. Additionally, smaller species may have many more ecological niches available to them and thus facilitating the diversification of life (Hutchinson and MacArthur, 1959[1]).

Larger organisms require more food overall (Blackburn and Gaston, 1997[18]), however they require less energy per unit of body mass. As a result, larger species are able to survive on a lower quality diet than smaller species. For example, grazing animals make up for their poor quality diet by digesting food longer and are able to extract more energy from it (Maurer et al. 1992[7]). Smaller species tend to specialize in a habitat that can provide them with a high quality diet.

Habitat quality is highly variable and as a result smaller species tend to be present in less of their range. Instead, they are only found in patches of their range where there is good habitat. A correlate to this argument is that the opposite is true for larger species. Larger species have lower beta diversity and are replaced less frequently across landscapes and as a result tend to occupy more of their range (see Occupancy-abundance relationship relationships) (Brown and Maurer, 1989;[5] Brown and Nicoletto, 1991[3]). This mechanism likely contributes to the shift in body size-species richness distribution observed between continental and local scales.

Recently, the metabolic theory of ecology has been used to explain macroecological patterns. According to May (1978[9]) there is equal energy flow through all size classes of interacting organisms. This has implications for the number of individuals in each size class and potentially the number of species as well. May (1978[2]) was the first to describe a mathematical equation that could be used to explain the right hand side of the body size-species richness pattern . His equation states that the number of species (S) is proportional to the length (L) of the species raised to the exponent of negative two (${\displaystyle S=L^{-2}}$). This theory is based on data from many different terrestrial animals (mammals, birds, beetles, and butterflies) and has garnered further support from a more recent study by Rice and Gislason (1996).[19] These new results also demonstrate a slope of negative two with respect to the right side of the body size-species richness pattern in the fish assemblage of the North Sea. Whether a slope of -2 is universal and what the mechanisms are that underlie this theory remain unclear.

Figure 3. The Frequency distribution of North American land mammals (n=465). The figure shows a right skewed distribution, with a mode tending to smaller species (50–100 g). Redrawn from Brown and Maurer (1989).[5]