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从当前遗传多样性推断近期历史丰度。

Inferring recent historic abundance from current genetic diversity.

机构信息

Marine Evolution and Conservation, Centre of Evolutionary and Ecological Studies, University of Groningen, PO Box 11103 CC, Groningen, The Netherlands.

出版信息

Mol Ecol. 2013 Jan;22(1):22-40. doi: 10.1111/mec.12094. Epub 2012 Nov 26.

Abstract

Recent historic abundance is an elusive parameter of great importance for conserving endangered species and understanding the pre-anthropogenic state of the biosphere. The number of studies that have used population genetic theory to estimate recent historic abundance from contemporary levels of genetic diversity has grown rapidly over the last two decades. Such assessments often yield unexpectedly large estimates of historic abundance. We review the underlying theory and common practices of estimating recent historic abundance from contemporary genetic diversity, and critically evaluate the potential issues at various estimation steps. A general issue of mismatched spatio-temporal scales between the estimation itself and the objective of the estimation emerged from our assessment; genetic diversity-based estimates of recent historic abundance represent long-term averages, whereas the objective typically is an estimate of recent abundance for a specific population. Currently, the most promising approach to estimate the difference between recent historic and contemporary abundance requires that genetic data be collected from samples of similar spatial and temporal duration. Novel genome-enabled inference methods may be able to utilize additional information of dense genome-wide distributions of markers, such as of identity-by-descent tracts, to infer recent historic abundance from contemporary samples only.

摘要

近期历史丰度是保护濒危物种和了解前人类时代生物圈的重要参数,但很难确定。在过去的二十年中,利用种群遗传理论从当代遗传多样性水平估算近期历史丰度的研究数量迅速增加。此类评估通常会得出出人意料的大的历史丰度估算值。我们回顾了从当代遗传多样性估算近期历史丰度的基础理论和常见实践,并在各个估算步骤上对潜在问题进行了批判性评估。我们的评估结果表明,在估算本身和估算目标之间存在时空尺度不匹配的一般问题;基于遗传多样性的近期历史丰度估计代表长期平均值,而目标通常是特定种群的近期丰度估计。目前,最有前途的估算近期历史丰度和当代丰度之间差异的方法要求从具有相似时空持续时间的样本中收集遗传数据。新型基因组功能推断方法可能能够利用标记的密集全基因组分布的其他信息(例如,亲缘关系区段),仅从当代样本推断近期历史丰度。

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