Mammalian island biogeography: effects of area,isolation and vagility

Summary In this paper I reviewed mammalian biogeography for 19 archipelagoes and tested the applicability of the equilibrium theory of island biogeography to mammalian faunas in general. The species-area and species-isolation relationships of terrestrial mammals were consistent with the basic predictions of the equilibrium theory. The z-values for the species-area relationship did not differ significantly from Preston's canonical value of 0.26 (P>0.50), and the modal z-value for non-volant mammals was 0.25. Moreover, z-values increased with isolation and decreased with vagility of the fauna in question. Furthermore, the strength of the species-isolation correlation was negatively correlated with island area and vagility (P<0.001).     

Flea (Siphonaptera) species richness in the Great Basin Desert and island biogeography theory

Numbers of flea (Siphonaptera) species (flea species richness) on individual mammals should be higher on large mammals, mammals with dense populations, and mammals with large geographic ranges, if mammals are islands for fleas. I tested the first two predictions with regressions of H. J. Egoscue's trapping data on flea species richness collected from individual mammals against mammal size and population density from the literature. Mammal size and population density did not correlate with flea species richness. Mammal geographic range did, in earlier studies. The intermediate‐sized (31 g), moderately dense (0.004 individuals/m²) Peromyscus truei (Shufeldt) had the highest richness with eight flea species on one individual. Overall, island biogeography theory does not describe the distribution of flea species on mammals in the Great Basin Desert, based on H. J. Egoscue's collections. Alternatively, epidemiological or metapopulation theories may explain flea species richness.     

Leaves as islands for microbes

Summary The equilibrium theory of island biogeography provided a framework for describing the colonization of apple leaf islands by filamentous fungi. Surface sterilization of living leaves in situ by hydrogen peroxide allowed the colonization process to be followed from its inception. Numbers of species of filamentous fungi per leaf fluctuated from 6 to 21 during the first 2 weeks of colonization and equilibrated at about 12 by the third week. Turnover occurred in species composition at equilibrium. The equilibrium number of species was not related to leaf area.The presence of an equilibrium condition with turnover on the leaf surfaces is consistent with two key tenets of the theory of island biogeography. However, the apparent back of a species-area relationship is inconsistent with the island model.     

Mammalian species richness on islands on the Sunda Shelf,Southeast Asia

Summary A rich mammalian fauna is found on islands that lie on the Sunda Shelf, a continental shelf extending from Vietnam to Borneo and Java that was periodically exposed as dry land during the Pleistocene. The correlation between log of island area and number of species is high (r ²=0.94); the slope of the curve is moderate (z=0.235). Distance from small islands to source areas (=Borneo, Sumatra, and the Malay Peninsula) does not appear to affect species richness, nor does depth of water to source area (a measure of isolation time). A species-area curve for forest reserves of varying sizes on the Malay Peninsula has a low slope (z=0.104); comparison of the mainlaind and island curves indicates that decreasing island area is strongly correlated with increased extinction. Extinction has left reduced but ecologically balanced sets of species on all islands, except that carnivores are under-represented on all but the largest islands. Initial body size and rarity appear to play a significant role in determining the probability of extinction of individual species.     

Island biogeography of bats in Baja California, Mexico: patterns of bat species richness in a near-shore archipelago

Aim We studied the relationship between the size and isolation of islands and bat species richness in a near‐shore archipelago to determine whether communities of vagile mammals conform to predictions of island biogeography theory. We compared patterns of species richness in two subarchipelagos to determine whether area per se or differences in habitat diversity explain variations in bat species richness. Location Islands in the Gulf of California and adjacent coastal habitats on the Baja California peninsula in northwest Mexico. Methods Presence–absence surveys for bats were conducted on 32 islands in the Gulf of California using acoustic and mist‐net surveys. We sampled for bats in coastal habitats of four regions of the Baja peninsula to characterize the source pool of potential colonizing species. We fitted a semi‐log model of species richness and multiple linear regression and used Akaike information criterion model selection to assess the possible influence of log₁₀ area, isolation, and island group (two subarchipelagos) on the species richness of bats. We compared the species richness of bats on islands with greater vegetation densities in the southern gulf (n = 20) with that on drier islands with less vegetation in the northern gulf (n = 12) to investigate the relationship between habitat diversity and the species richness of bats. Results Twelve species of bats were detected on islands in the Gulf of California, and 15 species were detected in coastal habitats on the Baja peninsula. Bat species richness was related to both area and isolation of islands, and was higher in the southern subarchipelago, which has denser vegetation. Log₁₀ area was positively related to bat species richness, which increased by one species for every 5.4‐fold increase in island area. On average, richness declined by one species per 6.25 km increase in isolation from the Baja peninsula. Main conclusions Our results demonstrate that patterns of bat species richness in a near‐shore archipelago are consistent with patterns predicted by the equilibrium theory of island biogeography. Despite their vagility, bats may be more sensitive to moderate levels of isolation than previously expected in near‐shore archipelagos. Differences in vegetation and habitat xericity appear to be associated with richness of bat communities in this desert ecosystem. Although observed patterns of species richness were consistent with those predicted by the equilibrium theory, similar relationships between species richness and size and isolation of islands may arise from patch‐use decision making by individuals (optimal foraging strategies).     

Dispersal and establishment: spatial patterns and species–area relationships

According to the equilibrium theory of island biogeography, high colonization ability of species is associated with low exponents (z) of the species–area relationship (SAR) and weak spatial patterns in species number and dissimilarity. However, the relationship between z and the strength of these spatial patterns has not been investigated systematically. We used a multispecies metapopulation model to investigate these relationships in an archipelago of islands. We conclude that this relationship can only be predicted if either the dispersal ability or the power of establishment of species is known. With species richness limited by establishment, we generated high z‐values associated with weak spatial patterns in species number and dissimilarity. If species richness was constrained by the dispersal ability of species, we observed low to medium z‐values but strong spatial patterns. If the dispersal ability and the abilities of species to establish were both high, z‐values and spatial pattern tend to be low and species numbers were limited by the size of the regional species pool.     

The mammals of northern Melanesia: speciation,ecology, and biogeography

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island biogeography of Day Geckos (Phelsuma) in the Indian Ocean

Summary Step-wise multiple regression was employed to probe the determinants of species diversity of day geckos (Phelsuma) in the Indian Ocean. Independent variables were area, elevation, and two measures of isolation. Distance from Madagascar and island height (an indicator of habitat diversity) were the two most important predictors of species richness. Similar studies on other taxa rarely find isolation to be a major factor. The relatively poor dispersal abilities of reptiles may explain why isolation, rather than attributes of the islands, are more important in this case. The regressions also indicate that habitat diversity (assumed to correlate with maximum island elevation) is more important than area per se in determining species diversity. These results agree with predictions of the equilibrium theory of island biogeography, but historical processes have also greatly influenced species richness.     

Insular biogeography of the montane butterfly faunas in the Great Basin: comparison with birds and mammals

Summary Butterfly species lists were assembled for 18 Great Basin mountain ranges for which distributional data on mammals and birds have been analysed previously by other workers. The ranges represent remnant islands of the boreal habitat that once was continuous across the Great Basin but is now restricted to higher elevations as a result of climatic change at the close of the Pleistocene. The effects of biogeographic factors (area, distance, elevation) and habitat diversity on butterfly species number were examined. The Great Basin boreal butterfly faunas were found to be depauperate overall relative that of the principal mainland source, the Rocky Mountains, and were found to have fewer species than predicted by the mainland species-area data. However, only a weak area effect, and no distance effect, was detected by bivariate and multivariate analysis. Furthermore, the habitat diversity score found to explain virtually all the variation in bird species number in the same ranges in previous studies is only marginally significantly correlated with butterflies. When the butterflies are subdivided according to their vagility, the relative differences in the species-area correlation and slope (z-value) between the vagility categories were consistent with those found previously for mammals and birds, and, as predicted by theory, less vagile taxa exhibit higher species-area correlations and z-values. Overall, differences in the insular biogeography of buttterflies and vertebrates seem to reflect fundamental ecological differences between the taxa.     

Comparative biogeography of mammals on islands

Insular faunas of terrestrial mammals and bats are examined on a worldwide basis to test the adequacy of equilibrium and historical legacy models as explanations for species-area relationships. Species numbers of bats on islands conform to predictions from equilibrium theory, whereby recurrent immigrations and extinctions influence species richness. By contrast, species numbers of terrestrial mammals on islands result from a historical legacy of very low immigration rates on oceanic islands (the faunas are colonization-limited) and by the fragmentation of once contiguous continental faunas to form relictual populations, which subsequently undergo extinctions, on landbridge islands (the faunas are extinction-limited). This explanation is supported by several lines of evidence: (1) z values (slopes of species-area curves) are lower for non-volant mammals on oceanic islands than for those on landbridge islands, but are the opposite for bats; (2) z values for non-volant mammals are lower than those for bats on oceanic islands, but are higher than those for bats on landbridge islands; and (3) landbridge island faunas are attenuated mainland faunas, whereas those on oceanic islands are ecologically incomplete. No support is found for alternative hypotheses to explain low species-area slopes for terrestrial mammals on oceanic islands.     

Habitat islands and the equilibrium theory of island biogeography: testing some predictions

Summary Species-area data from a study of marsh birds are used to test five predictions generated by the equilibrium theory of island biogeography. Three predictions are supported: we found a significant species-area relationship, a non-zero level of turnover, and a variance-mean ratio of 0.5. One prediction is rejected: the extinction rates were not greater on small islands. The results of one test are equivocal: the number of species on each island was not always the same. As Gilbert (1980) suggests, a strong species-area relationship alone does not validate the theory. The avian communities we studied were on habitat islands, not true islands, and underwent complete extinction annually. Thus caution must be used before applying the theory to these and other habitat islands.     

Island biogeography theory explains the genetic diversity of a fragmented rock ptarmigan (Lagopus muta) population

The island biogeography theory is one of the major theories in ecology, and its applicability to natural systems is well documented. The core model of the theory, the equilibrium model of island biogeography, predicts that species diversity on an island is positively related to the size of the island, but negatively related by the island's distance to the mainland. In recent years, ecologists have begun to apply this model when investigating genetic diversity, arguing that genetic and species diversity might be influenced by similar ecological processes. However, most studies have focused on oceanic islands, but knowledge on how the theory applies to islands located on the mainland (e.g., mountain islands, forest islands) is scarce. In this study, we examined how the size and degree of isolation of mountain islands would affect the genetic diversity of an alpine bird, the rock ptarmigan (Lagopus muta). Within our study area, we defined the largest contiguous mountain area as the mainland, while smaller mountains surrounding the mainland were defined as islands. We found that the observed heterozygosity (H_o) was significantly higher, and the inbreeding coefficient (F_is) significantly lower, on the mainland compared to islands. There was a positive significant relationship between the unbiased expected heterozygosity (H_n.b.) and island size (log km²), but a negative significant relationship between H_o and the cost distance to the mainland. Our results are consistent with the equilibrium model of island biogeography and show that the model is well suited for investigating genetic diversity among islands, but also on islands located on the mainland.     

On the general dynamic model of oceanic island biogeography

Aim To investigate the biological meaning of equations used to apply the general dynamic model (GDM) of oceanic island biogeography proposed by R. J. Whittaker, K. A. Triantis and R. J. Ladle. Location Analyses are presented for 17 animal groups living on the Aeolian Islands, a volcanic archipelago in the central Mediterranean, near Sicily. Methods In addition to the mathematical implementation of the GDM proposed by Whittaker, Triantis and Ladle, and termed here logATT² (, where S is species number or any other diversity metric, t is island age, A is island area, and a, b, c and d are fitted parameters), a new implementation based on the Arrhenius equation of the species–area relationship (SAR) is investigated. The new model (termed powerATT²) is: . For logATT² and powerATT² models, equations were developed to calculate (1) the expected number of species at equilibrium (i.e. when the island has reached maturity) per unit area (S_eq), and (2) the time required to obtain this value (t_eq). Whereas the intercept in the Gleason model (S = C + z log A) or the coefficient of the Arrhenius power model (S = CA^z) of the SAR can be considered measures of the expected number of species per unit area, this is not the case for the parameter a of the ATT² models. However, values of S_eq can be used for this purpose. The index of ‘colonization ability’ (CAB), calculated as the ratio , may provide a measure of the mean number of species added per unit area per unit time. Results Both ATT² models fitted most of the data well, but the powerATT² model was in most cases superior. Equilibrial values of species richness (S_eq) varied from c. 3 species km^?2 (reptiles) to 100 species km^?2 (mites). The fitted curves for the powerATT² model showed large variations in d, from 0.03 to 3. However, most groups had values of d around 0.2–0.4, as commonly observed for the z‐values of SARs modelled by a power function. Equilibration times ranged from about 170,000 years to 400,000 years. Mites and springtails had very high values of CAB, thus adding many more species per unit area per unit time than others. Reptiles and phytophagous scarabs showed very low values, being the groups that added fewest species per unit area per unit time. Main conclusions Values of equilibrial species richness per unit area are influenced by species biology (e.g. body size and ecological specialization). Theoretical and empirical evidence suggests that higher immigration rates should increase the z‐values of the Arrhenius model. Thus, in the same archipelago, groups with larger z‐values should be characterized by higher dispersal ability. Results obtained here for the parameter d conform to this prediction.     

Prairie dog towns as islands: applications of island biogeography and landscape ecology for conserving nonvolant terrestrial vertebrates

Aim To evaluate the utility of island biogeography theory as a model for understanding and conserving native communities of nonvolant terrestrial vertebrates at prairie dog towns. Location Oklahoma Panhandle, USA. Methods We surveyed mammal, reptile and amphibian communities on 36 black‐tailed prairie dog (Cynomys ludovicianus) towns during the summers and falls of 1997 to 1999. We used a Geographic Information System (GIS) to characterize the landscape within 10 km of each town. We used Principal Components Analysis (PCA), Correlation Analysis, and Linear Regression to test for patterns in species richness relative to area and isolation of towns, local habitat characteristics, and characteristics of the adjacent landscape. Results Species richness was not significantly correlated with town size, town isolation, or local habitat characteristics. On the other hand, species richness was significantly correlated with characteristics of the landscape within 10 km of the focal town. In addition, species richness of mammals at prairie dog towns during the summer increased in a northerly direction, while richness of mammals at towns during fall increased to the west. Main conclusions These results, albeit contrary to traditional island biogeography theory, are consistent with an emerging view that communities on relatively small islands are strongly influenced by characteristics of the adjacent landscape (or seascape). We recommend that to the extent possible, networks of reserves for prairie dogs and their associated species should include clusters of large towns (i.e. larger than those studied here), as well as large but isolated towns, and that conservation efforts should include management of the intervening matrix of anthropogenic habitats.     

Lakes and rivers as islands: species-area relationships in the fish faunas of Ontario

Synopsis Fish species richness in 82 lakes in Ontario, Canada was significantly correlated with surface area. In this region, latitude explained only a small amount of the variation in fish species richness. Thus, our study provides a clear demonstration of the relation between fish species richness and lake area without the confounding effects of latitude and physiography inherent in analyses from broader geographic regions. By comparison with the species-area relationship obtained, we show that acidification clearly depressed the number of fish species in 66 acid-stressed lakes in Ontario. Fish species richness was also significantly correlated with both drainage and surface areas of 21 Ontario rivers. Slopes of species-area regressions of lakes and rivers did not differ significantly, suggesting that species are added to these habitats at similar rates. However, our regression analyses show that rivers support more species of fish per unit surface area of water. Although these results are consistent with some predictions of island biogeography theory, we suggest that fish species richness is more likely to be a simple function of habitat diversity, rather than an equilibrial balance between immigration and extinction.     

A unified model of island biogeography sheds light on the zone of radiation

Islands acquire species through immigration and speciation. Models of island biogeography should capture both processes; however quantitative island biogeography theory has either neglected speciation or treated it unrealistically. We introduce a model where the dominance of immigration on small and near islands gives way to an increasing role for speciation as island area and isolation increase. We examine the contribution of immigration and speciation to the avifauna of 35 archipelagoes and find, consistent with our model, that the zone of radiation comprises two regions: endemic species diverged from mainland sister-species at intermediate isolation and from insular sister-species at higher levels of isolation. Our model also predicts species-area curves in accord with existing research and makes new predictions about species ages and abundances. We argue that a paucity of data and theory on species abundances on isolated islands highlights the need for island biogeography to be reconnected with mainstream ecology.     

Oceanic island biogeography through the lens of the general dynamic model: assessment and prospect

The general dynamic model of oceanic island biogeography (GDM) has added a new dimension to theoretical island biogeography in recognizing that geological processes are key drivers of the evolutionary processes of diversification and extinction within remote islands. It provides a dynamic and essentially non‐equilibrium framework generating novel predictions for emergent diversity properties of oceanic islands and archipelagos. Its publication in 2008 coincided with, and spurred on, renewed attention to the dynamics of remote islands. We review progress, both in testing the GDM's predictions and in developing and enhancing ecological–evolutionary understanding of oceanic island systems through the lens of the GDM. In particular, we focus on four main themes: (i) macroecological tests using a space‐for‐time rationale; (ii) extensions of theory to islands following different patterns of ontogeny; (iii) the implications of GDM dynamics for lineage diversification and trait evolution; and (iv) the potential for downscaling GDM dynamics to local‐scale ecological patterns and processes within islands. We also consider the implications of the GDM for understanding patterns of non‐native species diversity. We demonstrate the vitality of the field of island biogeography by identifying a range of potentially productive lines for future research.     

Between-group differences in the Iberian dung beetle species-area relationship (Coleoptera: Scarabaeidae)

Between-group α- and β-diversity differences were derived from species-area relationships fitted to field data. The accuracy of spatial richness variation predictions based on area size was also checked. The log-log model (log S = c + z log A) was found to be the best-fit linear model, with slopes (z) ranging from 0.089 to 0.142. Between-group comparisons of z (slope) and q (intercept) parameters, using the S = q + cA^z curvilinear regression model, corroborated early results, indicating a lower β-diversity (slope) for Scarabaeinae than for Geotrupinae and Aphodiinae. The latter group, probably more sensitive to environmental heterogeneity, should contribute more to species richness in large areas. α-Diversity is greater for Aphodiinae, more relevant to local diversity (1 km²), than for Scarabaeinae and considerably greater for these two groups than for Geotrupinae. As earlier results show that the richness of a single dung pat is rather more a function of the Scarabaeinae species pool, richness on dung pat scales is probably due more to the between-dropping mobile Scarabaeinae, while Aphodiinae contribute mainly to local and regional pool richness. Nearly 88 % of the total richness variance is explained by area size. This percentage decreases to 37 % when the spatial structure of area size and species number are extracted. The corresponding figures for Scarabaeinae, Aphodiinae and Geotrupinae are 44, 22 and 31 %, respectively.     

Scale-dependent equilibrium in highly heterogeneous islands: plant geography of the northern Great Barrier Reef sand cays and shingle islets

In contrast to classical island biogeographical predictions, plant species richness is not monotonically related to island area or isolation for the northern Great Barrier Reef islands, and this cannot be accounted for as a ‘small island effect’. Many islands are composed of different terrain units bearing different floristic assemblages suggesting a modified‘terrain-floristic element’model for island biogeography. This requires definition of a time-scale for equilibrium considerations and emphasizes that equilibrium or first order perturbation (‘relaxation’) models may be inappropriate for some archipelagos.     

千岛湖陆桥岛屿鸟类集团对栖息地片段化的敏感性及其季节变化

为探究千岛湖陆桥岛屿不同鸟类集团对栖息地片段化敏感性的差异和季节变化,于2009年4月—2012年1月鸟类繁殖季(4、5、6月)和冬季(11、12、1月)对千岛湖41个陆桥岛屿鸟类集团进行了研究。结果表明,冬季杂食鸟对片段化敏感性高于食虫鸟,繁殖季时二者无显著差异,繁殖季和冬季时下层鸟对片段化敏感性均高于林冠鸟,冬季留鸟对片段化敏感性高于候鸟,繁殖季则无显著差异。杂食鸟和留鸟对片段化敏感性存在季节差异,而食虫鸟、林冠鸟、下层鸟和候鸟对片段化敏感性均无季节差异。不同鸟类集团对栖息地片段化敏感性的差异和季节变化规律,有助于人们在栖息地管理和保护区设计时采取更有针对性的鸟类保护措施。