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John‐Arvid Grytnes John H. Beaman Tom S. Romdal Carsten Rahbek 《Journal of Biogeography》2008,35(11):2138-2147
Aim In simulation exercises, mid‐domain peaks in species richness arise as a result of the random placement of modelled species ranges within simulated geometric constraints. This has been called the mid‐domain effect (MDE). Where close correspondence is found between such simulations and empirical data, it is not possible to reject the hypothesis that empirical species richness patterns result from the MDE rather than being the outcome (wholly or largely) of other factors. To separate the influence of the MDE from other factors we therefore need to evaluate variables other than species richness. The distribution of range sizes gives different predictions between models including the MDE or not. Here, we produce predictions for species richness and distribution of range sizes from one model without the MDE and from two MDE models: a classical MDE model encompassing only species with their entire range within the domain (range‐restricted MDE), and a model encompassing all species with the theoretical midpoint within the domain (midpoint‐restricted MDE). These predictions are compared with observations from the elevational pattern of range‐size distributions and species richness of vascular plants. Location Mount Kinabalu, Borneo. Methods The data set analysed comprises more than 28,000 plant specimens with information on elevation. Species ranges are simulated with various assumptions for the three models, and the species simulated are subsequently subjected to a sampling that simulates the actual collection of species on Mount Kinabalu. The resulting pattern of species richness and species range‐size distributions are compared with the observed pattern. Results The comparison of simulated and observed patterns indicates that an underlying monotonically decreasing trend in species richness with elevation is essential to explain fully the observed pattern of richness and range size. When the underlying trend is accounted for, the MDE model that restricts the distributions of theoretical midpoints performs better than both the classical MDE model and the model that does not incorporate geometric constraints. Main conclusions Of the three models evaluated here, the midpoint‐restricted MDE model is found to be the best for explaining species richness and species range‐size distributions on Mount Kinabalu. 相似文献
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Zhongzheng Chen Xueyou Li Wenyu Song Quan Li Kenneth Onditi Laxman Khanal Xuelong Jiang 《Ecology and evolution》2020,10(5):2545-2558
Understanding the species diversity patterns along elevational gradients is critical for biodiversity conservation in mountainous regions. We examined the elevational patterns of species richness and turnover, and evaluated the effects of spatial and environmental factors on nonvolant small mammals (hereafter “small mammal”) predicted a priori by alternative hypotheses (mid‐domain effect [MDE], species–area relationship [SAR], energy, environmental stability, and habitat complexity]) proposed to explain the variation of diversity. We designed a standardized sampling scheme to trap small mammals at ten elevational bands across the entire elevational gradient on Yulong Mountain, southwest China. A total of 1,808 small mammals representing 23 species were trapped. We observed the hump‐shaped distribution pattern of the overall species richness along elevational gradient. Insectivores, rodents, large‐ranged species, and endemic species richness showed the general hump‐shaped pattern but peaked at different elevations, whereas the small‐ranged species and endemic species favored the decreasing richness pattern. The MDE and the energy hypothesis were supported, whereas little support was found for the SAR, the environmental stability hypothesis, and the habitat complexity. However, the primary driver(s) for richness patterns differed among the partitioning groups, with NDVI (the normalized difference vegetation index) and MDE being the most important variables for the total richness pattern. Species turnover for all small mammal groups increased with elevation, and it supported a decrease in community similarity with elevational distance. Our results emphasized for increased conservation efforts in the higher elevation regions of the Yulong Mountain. 相似文献
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Ecological, evolutionary, spatial and neutral theories make distinct predictions and provide distinct explanations for the mechanisms that control the relationship between diversity and the environment. Here, we test predictions of the elevational diversity gradient focusing on Iberian bumblebees, grasshoppers and birds. Processes mediated by local abundance and regional diversity concur in explaining local diversity patterns along elevation. Effects expressed through variation in abundance were similar among taxa and point to the overriding role of a physical factor, temperature. This determines how energy is distributed among individuals and ultimately how the resulting pattern of abundance affects species incidence. Effects expressed through variation in regional species pools depended instead on taxon‐specific evolutionary history, and lead to diverging responses under similar environmental pressures. Local filters and regional variation also explain functional diversity gradients, in line with results from species richness that indicate an (local) ecological and (regional) historical unfolding of diversity–elevation relationships. 相似文献
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Robert K. Colwell Nicholas J. Gotelli Louise A. Ashton Jan Beck Gunnar Brehm Tom M. Fayle Konrad Fiedler Matthew L. Forister Michael Kessler Roger L. Kitching Petr Klimes Jürgen Kluge John T. Longino Sarah C. Maunsell Christy M. McCain Jimmy Moses Sarah Noben Katerina Sam Legi Sam Arthur M. Shapiro Xiangping Wang Vojtech Novotny 《Ecology letters》2016,19(9):1009-1022
We introduce a novel framework for conceptualising, quantifying and unifying discordant patterns of species richness along geographical gradients. While not itself explicitly mechanistic, this approach offers a path towards understanding mechanisms. In this study, we focused on the diverse patterns of species richness on mountainsides. We conjectured that elevational range midpoints of species may be drawn towards a single midpoint attractor – a unimodal gradient of environmental favourability. The midpoint attractor interacts with geometric constraints imposed by sea level and the mountaintop to produce taxon‐specific patterns of species richness. We developed a Bayesian simulation model to estimate the location and strength of the midpoint attractor from species occurrence data sampled along mountainsides. We also constructed midpoint predictor models to test whether environmental variables could directly account for the observed patterns of species range midpoints. We challenged these models with 16 elevational data sets, comprising 4500 species of insects, vertebrates and plants. The midpoint predictor models generally failed to predict the pattern of species midpoints. In contrast, the midpoint attractor model closely reproduced empirical spatial patterns of species richness and range midpoints. Gradients of environmental favourability, subject to geometric constraints, may parsimoniously account for elevational and other patterns of species richness. 相似文献
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Both our analysis ( Kerr et al. 2006 ), and Lees and Colwell's (2007) reanalysis, of patterns of bird and mammal diversity on Madagascar show that the central peak of richness predicted by the Mid‐Domain Hypothesis (MDH) is not observed. Lees and Colwell emphasize an observation consistent with MDH predictions: a latitudinal mid‐domain richness peak in the rainforest biome. They find (but do not mention) that no analogous peak is observed in the other two main Madagascan biomes. MDH fails nearly all its tests in Madagascar. 相似文献
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Grégory Beaugrand Isabelle Rombouts Richard R Kirby 《Global Ecology and Biogeography》2013,22(4):440-449
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Manly 《Ecology letters》1998,1(2):104-111
Testing for a relationship between the body size of animals and a gradient such as latitude is complicated by the fact that typically there is a single average size for each species, and each species occurs at several sample stations over the gradient. This results in standard tests for statistical significance being invalid. This problem can be overcome by using a randomization test. A more difficult problem, however, is determining whether the relationship between size and latitude is the same for two subfamilies of species. In this paper a general method for relating body size to latitude and subfamily differences is proposed, with the significance of effects determined by randomization. A simulation study suggests that this procedure has good properties. This approach to data analysis has promise both for the particular situation considered and for other related problems in biogeography. 相似文献
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Could temperature and water availability drive elevational species richness patterns? A global case study for bats 总被引：2，自引：0，他引：2
Christy M. McCain 《Global Ecology and Biogeography》2007,16(1):1-13
Aim A global meta‐analysis was used to elucidate a mechanistic understanding of elevational species richness patterns of bats by examining both regional and local climatic factors, spatial constraints, sampling and interpolation. Based on these results, I propose the first climatic model for elevational gradients in species richness, and test it using preliminary bat data for two previously unexamined mountains. Location Global data set of bat species richness along elevational gradients from Old and New World mountains spanning 12.5° S to 38° N latitude. Methods Bat elevational studies were found through an extensive literature search. Use was made only of studies sampling 70% of the elevational gradient without significant sampling biases or strong anthropogenic disturbance. Undersampling and interpolation were explicitly examined with three levels of error analyses. The influence of spatial constraints was tested with a Monte Carlo simulation program, Mid‐Domain Null. Preliminary bat species richness data sets for two test mountains were compiled from specimen records from 12 US museum collections. Results Equal support was found for decreasing species richness with elevation and mid‐elevation peaks. Patterns were robust to substantial amounts of error, and did not appear to be a consequence of spatial constraints. Bat elevational richness patterns were related to local climatic gradients. Species richness was highest where both temperature and water availability were high, and declined as temperature and water availability decreased. Mid‐elevational peaks occurred on mountains with dry, arid bases, and decreasing species richness occurred on mountains with wet, warm bases. A preliminary analysis of bat richness patterns on elevational gradients in western Peru (dry base) and the Olympic Mountains, WA (wet base), supported the predictions of the climate model. Main conclusions The relationship between species richness and combined temperature and water availability may be due to both direct (thermoregulatory constraints) and indirect (food resources) factors. Abundance was positively correlated with species richness, suggesting that bat species richness may also be related to productivity. The climatic model may be applicable to other taxonomic groups with similar ecological constraints, for instance certain bird, insect and amphibian clades. 相似文献
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Dirk Nikolaus Karger Jürgen Kluge Thorsten Krömer Andreas Hemp Marcus Lehnert Michael Kessler 《Journal of Biogeography》2011,38(6):1177-1185
Aim To calculate the degree to which differences between local and regional elevational species richness patterns can be accounted for by the effects of regional area. Location Five elevational transects in Costa Rica, Ecuador, La Réunion, Mexico and Tanzania. Methods We sampled ferns in standardized field plots and collated regional species lists based on herbarium and literature data. We then used the Arrhenius function S = cAz to correct regional species richness (S) for the effect of area (A) using three slightly different approaches, and compared the concordance of local and regional patterns prior to and after accounting for the effect of area on regional richness using linear regression analyses. Results We found a better concordance between local and regional elevational species richness after including the effect of area in the majority of cases. In several cases, local and regional patterns are very similar after accounting for area. In most of the cases, the maximum regional richness shifted to a higher elevation after accounting for area. Different approaches to correct for area resulted in qualitatively similar results. Main conclusions The differences between local and regional elevational richness patterns can at least partly be accounted for by area effects, suggesting that the underlying causes of elevational richness patterns might be the same at both spatial scales. Values used to account for the effect of area differ among the different study locations, showing that there is no generally applicable elevational species–area relationship. 相似文献
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Robert R. Dunn T. Jonathan Davies Nyeema C. Harris Michael C. Gavin 《Proceedings. Biological sciences / The Royal Society》2010,277(1694):2587-2595
The differences in the richness and prevalence of human pathogens among different geographical locations have ramifying consequences for societies and individuals. The relative contributions of different factors to these patterns, however, have not been fully resolved. We conduct a global analysis of the relative influence of climate, alternative host diversity and spending on disease prevention on modern patterns in the richness and prevalence of human pathogens. Pathogen richness (number of kinds) is largely explained by the number of birds and mammal species in a region. The most diverse countries with respect to birds and mammals are also the most diverse with respect to pathogens. Importantly, for human health, the prevalence of key human pathogens (number of cases) is strongly influenced by disease control efforts. As a consequence, even where disease richness is high, we might still control prevalence, particularly if we spend money in those regions where current spending is low, prevalence is high and populations are large. 相似文献
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Jianjun Wang Janne Soininen Yong Zhang Beixin Wang Xiangdong Yang Ji Shen 《Journal of Biogeography》2011,38(3):595-603
Aim Data and analyses of elevational gradients in diversity have been central to the development and evaluation of a range of general theories of biodiversity. Elevational diversity patterns have, however, been severely understudied for microbes, which often represent decomposer subsystems. Consequently, generalities in the patterns of elevational diversity across different trophic levels remain poorly understood. Our aim was to examine elevational gradients in the diversity of macroinvertebrates, diatoms and bacteria along a stony stream that covered a large elevational gradient. Location Laojun Mountain, Yunnan province, China. Methods The sampling scheme included 26 sites spaced at elevational intervals of 89 m from 1820 to 4050 m elevation along a stony stream. Macroinvertebrate and diatom richness were determined based on the morphology of the specimens. Taxonomic richness for bacteria was quantified using a molecular fingerprinting method. Over 50 environmental variables were measured at each site to quantify environmental variables that could correlate with the patterns of diversity. We used eigenvector‐based spatial filters with multiple regressions to account for spatial autocorrelation. Results The bacterial richness followed an unexpected monotonic increase with elevation. Diatoms decreased monotonically, and macroinvertebrate richness showed a clear unimodal pattern with elevation. The unimodal richness pattern for macroinvertebrates was best explained by the mid‐domain effect (r2 = 0.72). The diatom richness was best explained by the variation in nutrient supply, and the increase in bacterial richness with elevation may be related to an increased carbon supply. Main conclusions We found contrasting patterns in elevational diversity among the three studied multi‐trophic groups comprising unicellular and multicellular aquatic taxa. We also found that there may be fundamental differences in the mechanisms underlying these species diversity patterns. 相似文献
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Phyo Kay Khine Jürgen Kluge Michael Kessler Georg Miehe Dirk N. Karger 《Journal of Biogeography》2019,46(5):981-991
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Mark Westoby;Samuel C. Andrew;Rachael V. Gallagher;Julian Schrader; 《Oikos》2024,2024(4):e10556
With climate zones moving poleward, it is interesting to know how rapidly species are gained and lost along temperature gradients. For the Australian native vascular flora, observed climate envelopes for species distributions have here been calculated from data for occurrence at geographical locations. For each degree temperature increase along a continental temperature gradient, numbers of species crossing their cold boundary and hence added to the flora, and crossing their warm boundary and hence lost to the flora, were counted. These counts of gains and losses were expressed as percentages of the flora recorded as present at that temperature. We report results for the flora at > 700 mm rainfall pa along the Australian east coast, where higher rainfall is continuously distributed throughout the latitudinal range. Per °C mean annual temperature increase, 20 ± 11% (mean ± SD) of species were gained, and 14 ± 4% were lost, across the range 9–23°C. Many further questions arise. For example, which other continental floras might show faster or slower rates of species gain and loss along temperature gradients? Similarly, might species with particular traits show faster rates of turnover: for example, species with local dispersal such as those with diaspore morphologies adapted for ants, compared to those adapted for bird dispersal? 相似文献
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Aim To test whether the temperature dependence of individuals’ metabolic rates is the mechanism shaping broad‐scale species‐richness gradients as proposed in the Metabolic Theory of Ecology recently proposed by Allen, Gillooly and Brown. Location North America, north of Mexico. Methods Metabolic Theory predicts that the natural logarithm of species richness will be a linear function of environmental temperature ((kT)−1, where k is Boltzmann's constant and T is temperature in K) with a slope of −0.78. We tested these predictions using the broad‐scale variation in richness of amphibians, reptiles, trees, tiger beetles, butterflies and blister beetles. We tested whether the temperature–richness relationship was linear or curvilinear, and determined the range of temperature values (and geographical area) where the instantaneous slope of the curvilinear temperature–richness relationship was statistically indistinguishable from −0.78, after correcting for spatial autocorrelation. Results We found that for all taxa, temperature–richness relationships were curvilinear. Moreover, for five of six taxa, the slope of this relationship was close to the predicted value for only a narrow range of temperatures. Blister beetles displayed the widest temperature range that is consistent with the Metabolic Theory, covering 45% of the study's geographical area. For the remaining taxa, the geographical range in which the slope is consistent with the predicted value amounts to only 10–20% of North America. Main conclusions For a wide array of taxa in North America, temperature–richness relationships deviate from the pattern predicted by Metabolic Theory. These results demonstrate that the temperature dependence of individuals’ metabolic rates is not the sole cause of broad‐scale diversity gradients. Even in areas where factors other than temperature do not influence productivity, the data do not suggest that richness patterns are determined by the temperature dependence of metabolic rate. 相似文献