黄海和东海梭子蟹种群遗传结构及幼虫传播策略

Mitochondrial Dna Pub Date : 2015-06-01 Epub Date: 2013-10-14 DOI:10.3109/19401736.2013.840592
Zhiqiang Han, Wei Zheng, Guobao Chen, Bonian Shui, Shufang Liu, Zhimeng Zhuang
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引用次数: 6

摘要

幼虫的扩散可能对底栖物种的遗传结构有重要影响。然而,不同的物种可能会选择不同的幼虫扩散策略。为研究双斑梭子蟹(Charybdis bimaculata)的种群遗传结构和幼虫传播策略,对其mtDNA COI基因658个碱基对(bp)片段进行了测序。在黄海和中国东部的5个地点共采集到67个个体,获得24个单倍型。5个种群的平均单倍型多样性和核苷酸多样性范围分别为0.2000±0.1541(舟山)~ 0.8333±0.1265(南麂岛)和0.0003±0.0005(舟山)~ 0.0026±0.0019(南麂岛)。分子变异分析和FST配对分析显示,黄海和东海对双马尾松的分布差异不显著,表明双马尾松具有较高的幼虫扩散能力,拒绝幼虫滞留。错配分布表明,双头草曾经历过种群扩张。幼虫在洋流中漂移,以及最近活动范围的扩大可能是研究区域遗传结构很少的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Population genetic structure and larval dispersal strategy of portunid crab Charybdis bimaculata in Yellow sea and East China sea.

Larval dispersal may have an important effect on genetic structure of benthic species. However, different species may choose different larval dispersal strategy. To examine the population genetic structure and larval dispersal strategy of portunid crab Charybdis bimaculata, a 658 base pair (bp) fragment of mtDNA COI gene was sequenced in this species. In total, 67 individuals were collected from 5 locations in Yellow Sea and East China, and 24 haplotypes were obtained. Mean haplotype diversity and nucleotide diversity for the five populations ranged from 0.2000 ± 0.1541 (Zhoushan) to 0.8333 ± 0.1265 (Nanji island), and from 0.0003 ± 0.0005 (Zhoushan) to 0.0026 ± 0.0019 (Nanji island). Analysis of molecular variance and pairwise FST revealed no significant differentiation between the Yellow Sea and the East China Sea in C. bimaculata, supporting high larval dispersal ability in this species, rejecting larval retention. Mismatch distribution revealed that C. bimaculata had undergone population expansion. Larval drift in the ocean currents, and recent range expansion could be the reasons for little genetic structure in the studied area.

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来源期刊
Mitochondrial Dna
Mitochondrial Dna 生物-遗传学
自引率
0.00%
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0
审稿时长
2.4 months
期刊介绍: Previously published under the title DNA Sequence (Vols 1-19.3), Mitochondrial DNA accepts original high-quality reports based on mapping, sequencing and analysis of mitochondrial DNA and RNA. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, medical genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The editorial board will also consider manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences.
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