Abstract

Genetic divergence of mitochondrial DNA does not necessarily correspond to reproductive isolation. However, if mitochondrial DNA lineages occupy separate segments of environmental space, this supports the notion of their evolutionary independence. We explore niche differentiation among three candidate species of crested newt (characterized by distinct mitochondrial DNA lineages) and interpret the results in the light of differences observed for recognized crested newt species. We quantify niche differences among all crested newt (candidate) species and test hypotheses regarding niche evolution, employing two ordination techniques (PCA-env and ENFA). Niche equivalency is rejected: all (candidate) species are found to occupy significantly different segments of environmental space. Furthermore, niche overlap values for the three candidate species are not significantly higher than those for the recognized species. As the three candidate crested newt species are, not only in terms of mitochondrial DNA genetic divergence, but also ecologically speaking, as diverged as the recognized crested newt species, our findings are in line with the hypothesis that they represent cryptic species. We address potential pitfalls of our methodology.

Highlights

  • Phylogeography has yielded a wealth of information by documenting geographical genetic variation [1]

  • Distribution and environmental data We composed a dataset of 2404 crested newt occurrences covering all recognized species and partitioned those for the T. karelinii group into three classes according to mitochondrial DNA: 120 T. carnifex, 1698 T. cristatus, 136 T. dobrogicus, 139 T. macedonicus, 135 T. karelinii west, 32 T. karelinii central and 144 T. karelinii east

  • The niche equivalency tests showed that niche overlap among species is significantly smaller than the null distribution (p = 0.198), meaning they occupy non-identical niche space

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Summary

Introduction

Phylogeography has yielded a wealth of information by documenting geographical genetic variation [1]. One key finding is the frequent presence of extensive mitochondrial DNA variation within taxa, not matched by morphological differentiation [2]. Translating such ‘cryptic diversity’ to species status would explicitly interpret mitochondrial DNA divergence as reflecting evolutionary independence. Genetic divergence of mitochondrial DNA is not necessarily a suitable proxy for the presence of species boundaries [3,4]. If geographical populations characterized by distinct mitochondrial DNA lineages (hereafter referred to as ‘candidate species’) occur under different ecological conditions, this increases support for their treatment as distinct species

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