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DNA 条形码在小型哺乳动物群落调查中的应用:苏里南实地研究。

DNA barcoding in surveys of small mammal communities: a field study in Suriname.

机构信息

Canadian Centre for DNA Barcoding, Biodiversity Institute of Ontario, University of Guelph, Guelph, Ontario, Canada N1G 2W1, Department of Natural History, Royal Ontario Museum, 100 Queen's Park, Toronto, Ontario, Canada M5S 2C6.

出版信息

Mol Ecol Resour. 2008 May;8(3):471-9. doi: 10.1111/j.1471-8286.2007.01998.x.

Abstract

The performance of DNA barcoding as a tool for fast taxonomic verification in ecological assessment projects of small mammals was evaluated during a collecting trip to a lowland tropical rainforest site in Suriname. We also compared the performance of tissue sampling onto FTA CloneSaver cards vs. liquid nitrogen preservation. DNA barcodes from CloneSaver cards were recovered from 85% of specimens, but DNA degradation was apparent, because only 36% of sequence reads were long (over 600 bp). In contrast, cryopreserved tissue delivered 99% barcode recovery (97% > 600 bp). High humidity, oversampling or tissue type may explain the poor performance of CloneSaver cards. Comparison of taxonomic assignments made in the field and from barcode results revealed inconsistencies in just 3.4% of cases and most of the discrepancies were due to field misidentifications (3%) rather than sampling/analytical error (0.5%). This result reinforces the utility of DNA barcoding as a tool for verification of taxonomic identifications in ecological surveys, which is especially important when the collection of voucher specimens is not possible.

摘要

在对苏里南低地热带雨林地区进行的小型哺乳动物生态评估项目的采集旅行中,评估了 DNA 条形码作为快速分类验证工具的性能。我们还比较了将组织样本置于 FTA CloneSaver 卡与液氮保存的性能。从 CloneSaver 卡中回收了 85%的标本的 DNA 条形码,但 DNA 降解明显,因为只有 36%的序列读取长度超过 600bp。相比之下,冷冻保存的组织可提供 99%的条形码回收率(97%> 600bp)。高湿度,过度采样或组织类型可能解释了 CloneSaver 卡性能不佳的原因。在野外和条形码结果中进行的分类分配比较仅在 3.4%的情况下不一致,并且大多数差异是由于野外误识别(3%)而不是采样/分析错误(0.5%)造成的。该结果证实了 DNA 条形码作为生态调查中分类鉴定验证工具的实用性,当不可能收集凭证标本时,这一点尤为重要。

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