Laboratorio de Ecología Molecular, Departamento de Oceanografía Biológica, Centro de Investigación Científica y de Educación Superior de Ensenada (CICESE), Ensenada, Baja California Sur, México.
Lab Applied Genomics, La Paz, Baja California Sur, México.
Mol Ecol Resour. 2021 Jul;21(5):1558-1574. doi: 10.1111/1755-0998.13375. Epub 2021 Mar 31.
Marine biodiversity can be surveyed using underwater visual censuses and recently with eDNA metabarcoding. Although a promising tool, eDNA studies have shown contrasting results related to its detection scale and the number of species identified compared to other survey methods. Also, its accuracy relies on complete reference databases used for taxonomic assignment and, as other survey methods, species detection may show false-negative and false-positive errors. Here, we compared results from underwater visual censuses and simultaneous eDNA metabarcoding fish surveys in terms of observed species and community composition. We also assess the effect of a custom reference database in the taxonomic assignment, and evaluate occupancy, capture and detection probabilities, as well as error rates of eDNA survey data. We amplified a 12S rRNA fish barcode from 24 sampling sites in the gulf of California. More species were detected with eDNA metabarcoding than with UVC. Because each survey method largely detected different sets of species, the combined approach doubled the number of species registered. Both survey methods recovered a known biodiversity gradient and a biogeographic break, but eDNA captured diversity over a broader geographic and bathymetric scale. Furthermore, the use of a modest-sized custom reference database significantly increased taxonomic assignment. In a subset of species, occupancy models revealed eDNA surveys provided similar or higher detection probabilities compared to UVC. The occupancy value of each species had a large influence on eDNA detectability, and in the false positive and negative error. Overall, these results highlight the potential of eDNA metabarcoding in complementing other established ecological methods for studies of marine fishes.
海洋生物多样性可以通过水下目视普查和最近的 eDNA 代谢组学来调查。尽管 eDNA 是一种很有前途的工具,但与其他调查方法相比,它的检测规模和识别物种的数量存在相互矛盾的结果。此外,它的准确性依赖于用于分类分配的完整参考数据库,并且与其他调查方法一样,物种检测可能会出现假阴性和假阳性错误。在这里,我们比较了水下目视普查和同时进行的 eDNA 代谢组学鱼类调查在观察到的物种和群落组成方面的结果。我们还评估了自定义参考数据库在分类分配中的作用,并评估了 eDNA 调查数据的占有率、捕获率和检测率以及错误率。我们从加利福尼亚湾的 24 个采样点扩增了 12S rRNA 鱼类条形码。与 UVC 相比,eDNA 代谢组学检测到了更多的物种。由于每种调查方法主要检测到不同的物种集合,因此联合方法使登记的物种数量增加了一倍。两种调查方法都恢复了已知的生物多样性梯度和生物地理断裂,但 eDNA 捕获的多样性具有更广泛的地理和水深尺度。此外,使用适度大小的自定义参考数据库可显著提高分类分配的效率。在一些物种中,占有模型表明,与 UVC 相比,eDNA 调查提供了相似或更高的检测概率。每个物种的占有值对 eDNA 的可检测性有很大影响,并且会影响假阳性和假阴性错误。总体而言,这些结果突出了 eDNA 代谢组学在补充其他已建立的海洋鱼类生态方法方面的潜力。