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A pilot study of fish biodiversity with a highlight of chondrichthyans in Hong Kong waters using environmental DNA metabarcoding

  • Rongjie Zhao
  • , Veronica Tsz Tung Lam
  • , Yifang Chen
  • , Jonathan Yat Fung Sit
  • , Jianlong Li
  • , Kenneth Mei Yee Leung
  • , Meng Yan*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

21 Downloads (CityUHK Scholars)

Abstract

Assessing marine fish biodiversity, particularly high trophic level and conservation value species like chondrichthyans (sharks, rays, and skates), is crucial for evaluating the health of local fisheries and the sustainability of coastal ecosystems. Hong Kong boasts a diverse coastal ecosystem and harbors a wide variety of marine fish species. Yet traditional fish survey methods often fall short of efficiently assessing local fish diversity. In this study, we employed the non-invasive environmental DNA (eDNA) method, to evaluate the overall fish diversity in Hong Kong, with a focus on chondrichthyans. We collected full-depth water samples from the eastern, southern, and western waters of Hong Kong. The primer set Elas12S was used to target chondrichthyans, while 12S_V5 was used to screen for all fish species. We successfully detected five chondrichthyan species (Scoliodon laticaudus, Scoliodon macrorhynchos, Gymnura japonica, Telatrygon zugei, and Hemitrygon bennettii), two of which are Near Threatened and two are Vulnerable according to the IUCN Red List. The eDNA data unveiled 136 fish species from 54 families within Hong Kong's coastal waters, with Mugil cephalus exhibiting the highest level of abundance. The indicator species utilized to assess environmental conditions differed substantially across distinct hydrographic zones. Our findings in this eDNA pilot study conducted in Hong Kong demonstrate that the eDNA method can be applied to detect targeted, vulnerable or near-threatened fish species, such as sharks and rays. Furthermore, this rapid detection methodology could have valuable applications for long-term biodiversity monitoring and marine conservation. To enhance the eDNA method and its accuracy in species identification, we recommend establishing a comprehensive reference database of DNA barcodes for local fish species and investigating appropriate sampling efforts in the highly diverse waters of Hong Kong. © 2025 The Authors.
Original languageEnglish
Article number104194
JournalRegional Studies in Marine Science
Volume86
Online published28 Apr 2025
DOIs
Publication statusPublished - Sept 2025

Funding

This project was conducted at the State Key Laboratory of Marine Pollution (SKLMP) and supported by the following funding sources: Shenzhen Science and Technology Program (Project No. JCYJ20220530140813030 to M Yan), three contract studies funded by the Agriculture, Fisheries and Conservation Department, the Government of Hong Kong SAR, China (AFCD/SQ/104/21/C, AFCD/SQ/90/21/C, and AFCD/FIS/01/19C to KMY Leung). This work was also supported by the Innovation and Technology Commission (ITC) of the Hong Kong SAR Government (9448002), which provides regular research funding support to SKLMP. However, any opinions, findings, conclusions, or recommendations expressed in this publication do not reflect the views of the Hong Kong SAR Government or the ITC. The authors thank Mr. Gabriel Y. Lee, Mr. Daniel Hong, Mr. Chun Ngai Lee, and Miss Lisa Catalan for their technical support in this study. The authors also thank the anonymous reviewers for their useful comments and suggestions on the manuscript.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 6 - Clean Water and Sanitation
    SDG 6 Clean Water and Sanitation
  2. SDG 14 - Life Below Water
    SDG 14 Life Below Water
  3. SDG 15 - Life on Land
    SDG 15 Life on Land

Research Keywords

  • 12S
  • EDNA
  • Elasmobranchii
  • Seawater
  • Subtropical region

Publisher's Copyright Statement

  • This full text is made available under CC-BY-NC-ND 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/

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