基因组证据表明,夏威夷珊瑚礁蝠鲼的岛屿居民种群数量较小,且行为具有性别偏见。

Jonathan L Whitney, Richard R Coleman, Mark H Deakos
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引用次数: 0

摘要

背景:珊瑚礁蝠鲼(Mobula alfredi)分布于全球热带和亚热带海域。它们的生活史特征(生长缓慢、晚熟、繁殖力低)使其容易受到干扰,因此需要采取明智的管理策略。以往的研究报告显示,大陆架沿线广泛的遗传连通性表明,跨越数百公里的连续栖息地基因流动性很高。然而,在夏威夷群岛,标签和照片识别证据表明,尽管岛屿种群距离很近,但它们是相互隔离的:结果:通过分析夏威夷岛和毛伊努伊岛(毛伊岛、摩洛卡伊岛、拉纳伊岛和卡霍奥拉维岛的四岛复合体)上的 M. alfredi(n = 38)之间的整个有丝分裂基因组单倍型和 2048 个核单核苷酸多态性(SNPs),对这一岛屿居住假说进行了检验。相对于核基因组全 SNPs(中性 FST = 0.003;离群 FST = 0.186),有丝分裂基因组(ΦST = 0.488)的强分化以及线粒体单倍型在岛屿间的聚类提供了强有力的证据,证明雌性暗礁蝠鲼具有强烈的亲缘性,不会在这两个岛屿群之间迁移。结合限制性的雄性迁移(相当于一只雄性蝠鲼每 2.2 代(约 64 年)在岛屿间迁移一次),我们提供了这些种群在人口统计学上明显孤立的证据。估计夏威夷岛和毛伊岛的当代有效种群数量(Ne)分别为 104(95% CI:99-110)和 129(95% CI:122-136):这些遗传学结果与照片识别和标签研究的证据一致,表明夏威夷的暗礁蝠鲼拥有小规模的、基因隔离的常驻岛屿种群。我们假设,由于岛屿质量效应(Island Mass Effect),大型岛屿提供了足够的资源来支持常住种群,因此没有必要穿越分隔岛屿群的深海峡。有效种群规模小、遗传多样性低、生活史特征为 K-选择,使得这些孤立的种群容易受到特定区域人为威胁的影响,这些威胁包括缠绕、船只撞击和栖息地退化。夏威夷群岛暗礁蝠鲼的长期生存需要因岛而异的管理策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genomic evidence indicates small island-resident populations and sex-biased behaviors of Hawaiian reef Manta Rays.

Genomic evidence indicates small island-resident populations and sex-biased behaviors of Hawaiian reef Manta Rays.

Genomic evidence indicates small island-resident populations and sex-biased behaviors of Hawaiian reef Manta Rays.

Genomic evidence indicates small island-resident populations and sex-biased behaviors of Hawaiian reef Manta Rays.

Background: Reef manta rays (Mobula alfredi) are globally distributed in tropical and subtropical seas. Their life history traits (slow growth, late maturity, low reproductive output) make them vulnerable to perturbations and therefore require informed management strategies. Previous studies have reported wide-spread genetic connectivity along continental shelves suggesting high gene flow along continuous habitats spanning hundreds of kilometers. However, in the Hawaiian Islands, tagging and photo-identification evidence suggest island populations are isolated despite proximity, a hypothesis that has not yet been evaluated with genetic data.

Results: This island-resident hypothesis was tested by analyzing whole mitogenome haplotypes and 2048 nuclear single nucleotide polymorphisms (SNPs) between M. alfredi (n = 38) on Hawai'i Island and Maui Nui (the 4-island complex of Maui, Moloka'i, Lāna'i and Kaho'olawe). Strong divergence in the mitogenome (ΦST = 0.488) relative to nuclear genome-wide SNPs (neutral FST = 0.003; outlier FST = 0.186), and clustering of mitochondrial haplotypes among islands provides robust evidence that female reef manta rays are strongly philopatric and do not migrate between these two island groups. Combined with restricted male-mediated migration, equivalent to a single male moving between islands every 2.2 generations (~ 64 years), we provide evidence these populations are significantly demographically isolated. Estimates of contemporary effective population size (Ne) are 104 (95% CI: 99-110) in Hawai'i Island and 129 (95% CI: 122-136) in Maui Nui.

Conclusions: Concordant with evidence from photo identification and tagging studies, these genetic results indicate reef manta rays in Hawai'i have small, genetically-isolated resident island populations. We hypothesize that due to the Island Mass Effect, large islands provide sufficient resources to support resident populations, thereby making crossing deep channels separating island groups unnecessary. Small effective population size, low genetic diversity, and k-selected life history traits make these isolated populations vulnerable to region-specific anthropogenic threats, which include entanglement, boat strikes, and habitat degradation. The long-term persistence of reef manta rays in the Hawaiian Islands will require island-specific management strategies.

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