Abstract

The general dynamic model of oceanic island biogeography integrates temporal changes in ecological circumstances with diversification processes, and has stimulated current research in island biogeography. In the original publication, a set of testable hypotheses was analysed using regression models: specifically, whether island data for four diversity indices are consistent with the ‘B~ATT2’ model, in which B is a diversity index, A is log(area) and T is time. The four indices were species richness, the number and percentage of single‐island endemic species, and a diversification index. Whether the relationships between these indices and time are unimodal (i.e., ‘hump‐shaped’) was a key focus, based on the characteristic ontogeny of a volcanic oceanic island. However, the significance testing unintentionally used zero, rather than the mean of the diversity index, as the null hypothesis, greatly inflating F‐ values and reducing P‐values compared with the standard regression approach. Here we first re‐analyze the data used to evaluate the general dynamic model in the seminal paper, using the standard null hypothesis, to provide an important qualification of its empirical results. This supports the significance of about half the original tests, the rest becoming non‐significant but mostly suggestive of the hypothesized relationship. Then we expand the original analysis by testing additional, theoretically derived functional relationships between the diversity indices, island area and time, within the framework of the ATT2 model and using a mixed‐effects modelling approach. This shows that species richness peaks earlier in island life‐cycles than endemism. Area has a greater effect on species richness and the number of single‐island endemics than on the proportion of single‐island endemics and the diversification index, and was always better fit as a log–log relationship than as a semi‐log one. Finally, the richness–time relationship is positively skewed, the initial rise happening much more quickly than the later decline.

Highlights

  • 2010) general dynamic model of oceanic island biogeography (GDM), currently the most comprehensive theoretical model for the biodiversity of oceanic islands of volcanic origi

  • The general linear and non-linear mixed-effects models supported these results for the B~lnATT2 model (Table S2)

  • The diversification index was best fit by a model without any time variable

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Summary

Introduction

2010) general dynamic model of oceanic island biogeography (GDM), currently the most comprehensive theoretical model for the biodiversity of oceanic islands of volcanic origin. The GDM is not an equilibrium theory and does not explicitly address interactions among the three fundamental processes of immigration, speciation and extinction Instead, it postulates that the carrying capacity (for species diversity) of an island, which is related to its topographic heterogeneity, increases as the island grows in area and elevation and declines as the island erodes away, later in its lifecycle. To minimize confounding influences of spatial or ecological context and regional biogeographic history, island archipelagos are often used for testing This was the case for Whittaker et al (2008), whose empirical evaluation of the GDM focused on the predicted unimodal relationship between time and the diversity-related indices, based on the typical ontogeny of volcanic islands. We test whether alternative theoretically based functional relationships between biodiversity indices and island area and time provide a better fit than those tested so far within the framework of the ATT2 approach

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