外来入侵吹蝇种群瓶颈造成的健康后果

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Ecology Pub Date : 2024-08-13 DOI:10.1111/mec.17492
Lilly Croft, Paige Matheson, Nathan J. Butterworth, Angela McGaughran
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引用次数: 0

摘要

入侵物种往往会经历人口瓶颈,导致遗传多样性减少,种群适应性也随之降低。尽管如此,它们仍能在新环境中茁壮成长。因此,研究近亲繁殖和遗传瓶颈对入侵物种种群适合度的影响是了解它们如何在新环境中生存的关键。我们利用原产于欧洲并被引入澳大利亚和新西兰的Calliphora vicina(Sciences, Mathématiques et Physique, 1830, 2, 1)来研究遗传多样性对种群适应性的影响。我们首先从新西兰的 15 个种群和澳大利亚的 1 个种群中收集了 59 个样本,并使用 20,501 个双偶联 SNP 调查了种群基因组的多样性、结构和混杂性。然后,我们通过建立近交系和远交系并测量各种适应性性状,探讨了重复实验瓶颈对种群适应性的影响。在野外捕获的样本中,我们发现了较低的总体遗传多样性、遗传掺杂信号和有限的((......)
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Fitness consequences of population bottlenecks in an invasive blowfly

Invasive species often undergo demographic bottlenecks that cause a decrease in genetic diversity and associated reductions in population fitness. Despite this, they manage to thrive in novel environments. Investigating the effects of inbreeding and genetic bottlenecks on population fitness for invasive species is, therefore, key to understanding how they may survive in new environments. We used the blowfly Calliphora vicina (Sciences, Mathématiques et Physique, 1830, 2, 1), which is native to Europe and was introduced to Australia and New Zealand, to examine the effects of genetic diversity on population fitness. We first collected 59 samples from 15 populations across New Zealand and one in Australia, and used 20,501 biallelic SNPs to investigate population genomic diversity, structure and admixture. We then explored the impacts of repeated experimental bottlenecks on population fitness by creating inbred and outbred lines of C. vicina and measuring a variety of fitness traits. In wild-caught samples, we found low overall genetic diversity, signals of genetic admixture and limited (<3%) genetic differentiation between North and South Island populations, with genetic links between the South Island and Australia. Following experimental bottlenecks, we found significant reductions in fitness for inbred lines. However, fitness effects were not felt equally across all phenotypic traits. Moreover, they were not enough to cause population collapse in any experimental line, suggesting that C. vicina (when under relaxed selection, as in laboratory settings) may be able to compensate for population bottlenecks even when highly inbred. Our results demonstrate the value of a tractable experimental system for investigating processes that may facilitate or hamper biological invasion.

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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
期刊最新文献
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