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Random sampling, abundance–extinction dynamics and niche‐filtering immigration constraints explain the generation of species richness gradients
Author(s) -
Carnicer Jofre,
Brotons Lluís,
Sol Daniel,
De Cáceres Miquel
Publication year - 2008
Publication title -
global ecology and biogeography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.164
H-Index - 152
eISSN - 1466-8238
pISSN - 1466-822X
DOI - 10.1111/j.1466-8238.2007.00380.x
Subject(s) - species richness , ecology , macroecology , extinction (optical mineralogy) , metacommunity , relative abundance distribution , abundance (ecology) , body size and species richness , ecological niche , niche , sampling (signal processing) , rank abundance curve , null model , biology , relative species abundance , biological dispersal , habitat , population , physics , species evenness , paleontology , demography , sociology , detector , optics
Aim The paradigm that species’ patterns of distribution, abundance and coexistence are the result of adaptations of the species to their niches has recently been challenged by evidence that similar patterns may be generated by simple random processes. We argue here that a better understanding of macroecological patterns requires an integration of both ecological and neutral stochastic approaches. We demonstrate the utility of such an integrative approach by testing the sampling hypothesis in a species–energy relationship of forest bird species. Location A Mediterranean biome in Catalonia, Spain. Methods To test the sampling hypothesis we designed a metacommunity model that reproduces the stochastic sampling from a regional pool to predict local species richness variation. Four conceptually different sampling procedures were evaluated. Results We showed that stochastic sampling processes predicted a substantial part (over 40%) of the observed variation in species richness, but left considerable variation unexplained. This remaining variation in species richness may be better understood as the result of alternative ecological processes. First, the sampling model explained more variation in species richness when the probability that a species colonises a new locality was assumed to increase with its niche width, suggesting that ecological differences between species matter when it comes to explaining macroecological patterns. Second, extinction risk was significantly lower for species inhabiting high‐energy regions, suggesting that abundance–extinction processes play a significant role in shaping species richness patterns. Main conclusions We conclude that species–energy relationships may not simply be understood as a result of either ecological or random sampling processes, but more likely as a combination of both.