Unveiling the hidden diversity of marine eukaryotes in the Ross Sea: A comparative analysis of seawater and sponge eDNA surveys

Author:

Jeunen Gert‐Jan12ORCID,Lamare Miles1,Cummings Vonda3,Treece Jackson2,Ferreira Sara2,Massuger Jack4,Pryor Rodgers Lily5,Tait Leigh5,Lust Bobby6,Wilkinson Shaun6,Mariani Stefano7ORCID,Mills Sadie3,Gemmell Neil2

Affiliation:

1. Marine Science Department University of Otago Dunedin New Zealand

2. Department of Anatomy, School of Biomedical Sciences University of Otago Dunedin New Zealand

3. National Institute of Water and Atmospheric Research (NIWA) Wellington New Zealand

4. National Institute of Water and Atmospheric Research (NIWA) Hamilton New Zealand

5. National Institute of Water and Atmospheric Research (NIWA) Christchurch New Zealand

6. Wilderlab NZ Ltd Wellington New Zealand

7. School of Biological and Environmental Sciences Liverpool John Moores University Liverpool UK

Abstract

AbstractThe Ross Sea, Antarctica, while largely pristine, is experiencing increased anthropogenic pressures, necessitating enhanced biomonitoring efforts for conservation purposes. Environmental DNA (eDNA) extracted from marine sponges provides a promising approach for biodiversity monitoring in remote areas by circumventing the need for time‐consuming water filtration. Investigations into the efficacy of eDNA signal detection across the tree of life from marine sponges have yet to be fully explored. Here, we conducted a seawater and sponge eDNA metabarcoding survey at seven coastal locations in the Ross Sea to assess spatial eukaryote biodiversity patterns and investigate eDNA signal differences between both substrates. In total, we detected 1450 operational taxonomic units (OTUs) across 30 phyla. Significant differences in water and sponge eDNA signal richness and composition were observed, with a partial overlap in OTU detection between both substrates and, thereby, underscoring the crucial role of substrate selection in eDNA metabarcoding surveys. Furthermore, alpha and beta diversity analyses revealed distinct eDNA signals among sampling locations, which were corroborated by known species distributions. However, only 135 OTUs (9%) could be successfully assigned to species level, and 574 OTUs (40%) were unable to be taxonomically classified, due to limitations in the reference database. Our results provide evidence for the potential of eDNA monitoring in remote areas, demonstrate the need to consider more sophisticated sampling strategies whereby multiple eDNA substrates are incorporated, and highlight the importance of complete reference databases for robust taxonomy assignment of eDNA signals.

Funder

Marsden Fund

Ministry of Business, Innovation and Employment

Publisher

Wiley

Subject

Genetics,Ecology,Ecology, Evolution, Behavior and Systematics

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