Abstract

Morphological differentiation associated with evolutionary diversification is often explained with adaptive benefits but the processes and mechanisms maintaining cryptic diversity are still poorly understood. Using genome‐wide data, we show here that the pale sand martin Riparia diluta in Central and East Asia consists of three genetically deeply differentiated lineages which vary only gradually in morphology but broadly reflect traditional taxonomy. We detected no signs of gene flow along the eastern edge of the Qinghai‐Tibetan plateau between lowland south‐eastern Chinese R. d. fohkienensis and high‐altitude R. d. tibetana. Largely different breeding and migration timing between these low and high altitude populations as indicated by phenology data suggests that allochrony might act as prezygotic isolation mechanism in the area where their ranges abut. Mongolian populations of R. d. tibetana, however, displayed signs of limited mixed ancestries with Central Asian R. d. diluta. Their ranges meet in the area of a well‐known avian migratory divide, where western lineages take a western migration route around the Qinghai‐Tibetan plateau to winter quarters in South Asia, and eastern lineages take an eastern route to Southeast Asia. This might also be the case between western R. d. diluta and eastern R. d. tibetana as indicated by differing wintering grounds. We hypothesize that hybrids might have nonoptimal intermediate migration routes and selection against them might restrict gene flow. Although further potential isolation mechanisms might exist in the pale sand martin, our study points towards contrasting migration behaviour as an important factor in maintaining evolutionary diversity under morphological stasis.

Highlights

  • How biodiversity is generated and maintained remains one of the main questions in evolutionary biology

  • Within R. diluta, Bayesian inference (BI) and maximum likelihood (ML) phylogenetic reconstructions recovered well supported clades mostly consistent with the distribution ranges of the morphologically-defined subspecies (Figure 1, Figure S1): One clade consisted of all samples of R. d. fohkienensis from lowland southeastern China, one of R. d. tibetana from the Qinghai-Tibetan Plateau and one of R. d. diluta from north-western China (Figure 1)

  • Samples collected from Mongolia in the potential breeding range of R. d. diluta, clustered and shared haplotypes with samples of R. d. tibetana from the Qinghai-Tibetan plateau

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Summary

Introduction

How biodiversity is generated and maintained remains one of the main questions in evolutionary biology. A considerable proportion of biodiversity may be constituted of ‘cryptic species’, i.e. evolutionary lineages with restricted gene flow that “do not form diagnostic morphological clusters” (Struck et al, 2018) Investigating their evolution is important to determine the processes under which biodiversity evolves in general and to increase our still limited understanding of diversification under morphological stasis in particular (Fišer et al, 2018). In the context of cryptic radiations, investigating evolutionary processes that might restrict gene flow among lineages lacking obvious morphological differences is crucial for our understanding on how diversity can be maintained in such cases We 3) investigated, if gene flow between phylogeographic lineages is reduced in areas of potential contact

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