Thea F. Rogers, Ewan H. Stenhouse, Hannah Wilson, Morgan Pendaries, Michael W. Bruford, Matthias Goetz, Pablo Orozco-terWengel
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Two mitochondrial DNA markers (cytochrome b and NADH subunit 4) and seven DNA microsatellite markers were used to assess the genetic diversity, genetic structure, demographic history, and effective population size of the two iguana populations. Mitochondrial DNA showed no genetic differentiation between populations; however, we found little to moderate divergence with microsatellites. We compared multiple demographic scenarios and revealed that ongoing gene flow is likely. The demographic history implied a significant genetic bottleneck around 10,000 years ago, coinciding with the sea level rise at the close of the last glacial period, and the start of the Holocene. Estimates of current effective population sizes indicate a small-scale number of breeders on each island of similar magnitude to the census mature population size (between 100 and 800 individuals). The relatively low differentiation between populations supports the possible development of active genetic management plans to manage the declining populations of the Sister Islands rock iguana.</p>","PeriodicalId":55212,"journal":{"name":"Conservation Genetics","volume":"69 1","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2024-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Using recent genetic history to inform conservation options of two Lesser Caymans iguana (Cyclura nubila caymanensis) populations\",\"authors\":\"Thea F. Rogers, Ewan H. Stenhouse, Hannah Wilson, Morgan Pendaries, Michael W. 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引用次数: 0
摘要
姊妹岛岩蜥(Cyclura nubila caymanensis)是加勒比海小开曼岛和开曼布拉克岛的特有物种,极度濒危。开曼布拉克岛的岩鬣蜥种群乃至整个物种都受到栖息地破坏、外来物种入侵以及人为因素对该岛造成的影响的威胁。我们评估了遗传多样性,估计了有效种群大小,并测试了这两个岛屿之间种群的分化情况,以便在将来需要对开曼布拉克种群进行迁移时为其提供信息。两个线粒体 DNA 标记(细胞色素 b 和 NADH 亚基 4)和七个 DNA 微卫星标记被用来评估两个鬣蜥种群的遗传多样性、遗传结构、人口历史和有效种群数量。线粒体 DNA 显示种群之间没有遗传差异;但是,我们发现微卫星的差异很小到中等程度。我们比较了多种人口统计情况,发现基因流很可能持续存在。人口统计历史表明,在距今约 1 万年前出现了严重的基因瓶颈,这与上一个冰川期结束时海平面上升以及全新世的开始相吻合。对目前有效种群数量的估计表明,每个岛上都有少量繁殖者,其数量与普查的成熟种群数量(100 至 800 只)相近。种群之间相对较低的分化支持制定积极的遗传管理计划,以管理姐妹群岛岩鬣蜥日益减少的种群。
Using recent genetic history to inform conservation options of two Lesser Caymans iguana (Cyclura nubila caymanensis) populations
The Sister Islands rock iguana (Cyclura nubila caymanensis) is critically endangered and endemic to the Caribbean islands Little Cayman and Cayman Brac. The Cayman Brac population and indeed the entire species is under threat from habitat destruction, invasive species, and anthropogenic impacts on the island. We assessed the genetic diversity, estimated effective population sizes, and tested for differentiation of populations between these two islands to inform potential future translocation should this be needed for the Cayman Brac population. Two mitochondrial DNA markers (cytochrome b and NADH subunit 4) and seven DNA microsatellite markers were used to assess the genetic diversity, genetic structure, demographic history, and effective population size of the two iguana populations. Mitochondrial DNA showed no genetic differentiation between populations; however, we found little to moderate divergence with microsatellites. We compared multiple demographic scenarios and revealed that ongoing gene flow is likely. The demographic history implied a significant genetic bottleneck around 10,000 years ago, coinciding with the sea level rise at the close of the last glacial period, and the start of the Holocene. Estimates of current effective population sizes indicate a small-scale number of breeders on each island of similar magnitude to the census mature population size (between 100 and 800 individuals). The relatively low differentiation between populations supports the possible development of active genetic management plans to manage the declining populations of the Sister Islands rock iguana.
期刊介绍:
Conservation Genetics promotes the conservation of biodiversity by providing a forum for data and ideas, aiding the further development of this area of study. Contributions include work from the disciplines of population genetics, molecular ecology, molecular biology, evolutionary biology, systematics, forensics, and others. The focus is on genetic and evolutionary applications to problems of conservation, reflecting the diversity of concerns relevant to conservation biology. Studies are based on up-to-date technologies, including genomic methodologies. The journal publishes original research papers, short communications, review papers and perspectives.