利用个体基因型将物候上不同步的飞蛾分配给源种群。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Patrick M A James, Julia T Fang, Julian Wittische, Michel Cusson, Jeremy Larroque, Amanda Roe, Rob Johns
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引用次数: 0

摘要

云杉budworm (Choristoneura fumiferana;SBW是一种周期性爆发的森林害虫,通过广泛的落叶和树木死亡影响北美北方森林。SBW暴发的广泛空间同步性的原因仍然是该物种生态学和管理中的一个关键问题。虽然莫兰效应(相关的有利环境条件)和密度依赖扩散(来自人口爆炸的中心)已经被提出并支持为同步爆发的驱动因素,但长距离扩散的相对贡献仍然知之甚少。在这项研究中,我们使用了一种新的方法来区分常驻飞蛾和迁徙飞蛾,并将迁徙飞蛾分配到可能的来源集群,目的是更好地表征区域扩散。首先,我们利用基因分型测序技术分析了一个飞行季节内居住的SBW幼虫和三个物候分离的飞蛾群体的遗传多样性和结构。然后,使用一种新颖的机器学习方法,我们将假定的移民分配给他们可能的源人群。我们假设迁徙蛾和常驻幼虫在遗传上是不同的,可以分配给源种群。研究结果揭示了单季节飞蛾种群分布和分化的复杂模式,包括两个空间重叠的遗传集群。我们观察到居住幼虫和迁徙飞蛾之间细微但显著的遗传差异,支持远距离扩散有助于爆发动态和同步性的假设。这些见解增强了我们对SBW种群动态的理解,并表明有效的管理战略,如早期干预战略(EIS),必须考虑到扩散在减轻重大疫情的有害影响方面的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assigning Phenologically Asynchronous Moths to Source Populations Using Individual Genotypes.

The spruce budworm (Choristoneura fumiferana; SBW) is a periodically outbreaking forest insect pest that affects the boreal forests of North America through extensive defoliation and tree mortality. Causes of widespread spatial synchrony of SBW outbreaks remain a key question in the ecology and management of this species. While the Moran effect (correlated favourable environmental conditions) and density-dependent dispersal (from epicentres of demographic explosions) have been proposed and supported as drivers of synchronised outbreaks, the relative contribution of long-distance dispersal is still poorly understood. In this study, we use a novel approach to distinguish resident from migrant moths and to assign migrants to likely source clusters with the goal of better characterising regional dispersal. First, we characterise the genetic diversity and structure of resident SBW larvae and three phenologically separated groups of moths over one flight season using Genotyping-by-Sequencing. Then, using a novel machine learning approach, we assign putative migrants to their likely source populations. We hypothesised that migrant moths and resident larvae would be genetically distinct and could be assigned to source populations. Our findings revealed complex patterns of moth dispersal and population differentiation within a single season, including two spatially overlapping genetic clusters. We observed subtle but significant genetic differences between resident larvae and migrant moths, supporting the hypothesis that long-distance dispersal contributes to outbreak dynamics and synchrony. These insights enhance our understanding of SBW population dynamics and suggest that effective management strategies, such as the Early Intervention Strategy (EIS), must account for the role of dispersal in mitigating the detrimental effects of major outbreaks.

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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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