岛屿两栖动物古代基因流动的水下走廊。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Miranda B. Sherlock, Mark Wilkinson, Simon T. Maddock, Ronald A. Nussbaum, Julia J. Day, Jeffrey W. Streicher
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引用次数: 0

摘要

许多群岛坐落在浅大陆架上,在更新世期间,随着冰川作用后全球海平面的下降,这些岛屿经常连接在一起。考虑到塞舌尔群岛的大陆架仅在海平面以下30-60米,在更新世期间,陆地生物群可能分散在现在孤立的岛屿上。在塞舌尔花岗岩的10个岛屿上发现了一种产卵、直接发育的蛭形两栖动物。尽管这种不耐盐的两栖动物的扩散能力似乎有限,但它在多个岛屿上的分布表明,它可能在历史上扩散过现在被淹没的大陆架走廊。我们使用精细基因组数据(ddRADseq)测试了这些历史走廊的遗传特征。我们发现基因组群通常不对应于群岛中的岛屿,距离隔离模式更符合连续景观中的基因流动,而不是孤立的岛屿种群。利用有效的迁移面和祖先范围扩展预测,我们发现当代种群起源于南部大岛mah附近,并通过孤立的fr门特岛分散到北部岛屿,并在塞舌尔河岸平坦的广阔地区进行了额外的历史性迁移。总的来说,我们的研究结果表明,生物地理模式可以保留来自更新世“古岛屿”的信号,而现在的岛屿可以被认为是承载瓶颈或短暂的避难所,而不是离散的遗传单位。因此,与古岛屿相关的基因流特征可能比当代岛屿对大陆架岛屿上陆生物种的隔离效应更强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Submerged Corridors of Ancient Gene Flow in an Island Amphibian

Submerged Corridors of Ancient Gene Flow in an Island Amphibian

Many island archipelagos sit on shallow continental shelves, and during the Pleistocene, these islands were often connected as global sea levels dropped following glaciation. Given a continental shelf only 30–60 m below sea level, the terrestrial biota of the Seychelles Archipelago likely dispersed amongst now isolated islands during the Pleistocene. Hypogeophis rostratus is an egg-laying, direct-developing caecilian amphibian found on 10 islands in the granitic Seychelles. Despite the seemingly limited dispersal abilities of this salt-intolerant amphibian, its distribution on multiple islands suggests likely historic dispersal across now submerged continental shelf corridors. We tested for the genetic signature of these historic corridors using fine-scale genomic data (ddRADseq). We found that genomic clusters often did not correspond to islands in the archipelago and that isolation-by-distance patterns were more consistent with gene flow across a continuous landscape than with isolated island populations. Using effective migration surfaces and ancestral range expansion prediction, we found support for contemporary populations originating near the large southern island of Mahé and dispersing to northern islands via the isolated Frégate island, with additional historic migration across the flat expanse of the Seychelles bank. Collectively, our results suggest that biogeographic patterns can retain signals from Pleistocene ‘palaeo-islands’ and that present-day islands can be thought of as hosting bottlenecks or transient refugia rather than discrete genetic units. Thus, the signatures of gene flow associated with palaeo-islands may be stronger than the isolating effects of contemporary islands in terrestrial species distributed on continental shelf islands.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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