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Evaluation of marine zooplankton community structure through environmental DNA metabarcoding

机译:通过环境DNA地区评估海洋浮游生儿群落结构

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Zooplankton dominate the abundance and biomass of multicellular animals in pelagic marine environments; however, traditional methods to characterize zooplankton communities are invasive and laborious. This study compares zooplankton taxonomic composition revealed through metabarcoding of the cytochrome oxidase I (COI) and 18S rRNA genes to traditional morphological identification by microscopy. Triplicates of three different sample types were collected from three coral reef sites in the Florida Keys National Marine Sanctuary: (1) 1 L surface seawater samples prefiltered through 3 lm filters and subsequently collected on 0.22 lm filters for eDNA (PF-eDNA); (2) 1 L surface seawater samples filtered on 0.22 lm pore-size filters (environmental DNA; eDNA), and (3) zooplankton tissue samples from 64 lm, 200 lm, and 500 lm mesh size net tows. The zooplankton tissue samples were split, with half identified morphologically and tissue DNA (T-DNA) extracted from the other half. The COI and 18S rRNA gene metabarcoding of PF-eDNA, eDNA, and T-DNA samples was performed using Illumina MiSeq. Of the families detected with COI and 18S rRNA gene metabarcoding, 40% and 32%, respectively, were also identified through morphological assessments. Significant differences in taxonomic composition were observed between PF-DNA, eDNA, and T-DNA with both genetic markers. PF-eDNA resulted in detection of fewer taxa than the other two sample types; thus, prefiltering is not recommended. All dominant copepod taxa (> 5% of total abundance) were detected with eDNA, T-DNA, and morphological assessments, demonstrating that eDNA metabarcoding is a promising technique for future biodiversity assessments of pelagic zooplankton in marine systems.
机译:浮游生统治在皮卡拉船上环境中的多细胞动物的丰富和生物量占主导地位;然而,传统方法表征浮游动物社区的侵入性和费力。该研究将浮游动物分类组合物通过微观氧化酶I(COI)和18S rRNA基因通过显微镜进行传统形态鉴定来揭示Zooplankton分类学组合物。从佛罗里达群岛国家海洋保护区的三个珊瑚礁地点收集三种不同样品类型的三倍瓶:(1)1 L表面海水样品穿过3 LM过滤器,随后收集0.22 LM过滤器的EDNA(PF-EDNA); (2)1 L表面海水样品在0.22 LM孔径过滤器(环境DNA; EDNA)上过滤,(3)Zooplankton组织样品,来自64 LM,200 LM和500 LM网格尺寸净轨道。 Zooplankton组织样品分裂,半鉴定为从另一半提取的形态学上和组织DNA(T-DNA)。使用Illumina miseq进行PF-EDNA,EDNA和T-DNA样品的COI和18S rRNA基因术。通过COI和18S rRNA基因检测到的家族,分别通过形态学评估鉴定了40%和32%。在PF-DNA,EDNA和T-DNA之间观察到分类组合物的显着差异,具有遗传标记。 PF-EDNA导致检测较少的分类群,而不是其他两个样品类型;因此,不建议预先改装。通过EDNA,T-DNA和形态学评估检测所有占优势桡足类税(占总丰度的5%),表明EDNA Metabarcoding是对海洋系统中未来生物多样性评估的有希望的技术。

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