Inter-Research > MEPS > v286 > p269-277  
Marine Ecology Progress Series

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MEPS 286:269-277 (2005)  -  doi:10.3354/meps286269

Shipboard identification of fish eggs and larvae by multiplex PCR, and description of fertilized eggs of blue marlin, shortbill spearfish, and wahoo

J. R. Hyde1,2,*, E. Lynn2, R. Humphreys Jr.3, M. Musyl4, A. P. West5, R. Vetter2

1Scripps Institution of Oceanography, 9500 Gilman Drive, La Jolla, California 92093-0203, USA
2Southwest Fisheries Science Center, National Marine Fisheries Service, NOAA, 8604 La Jolla Shores Drive, La Jolla,California 92037, USA
3Pacific Islands Fisheries Science Center, National Marine Fisheries Service, NOAA, 2570 Dole Street, Honolulu,Hawaii 96822, USA
4Pelagic Fisheries Research Program, Joint Institute for Marine and Atmospheric Research, University of Hawaii,Honolulu, Hawaii 96822, USA
5University of Technology Sydney, Westbourne St. Gore Hill, New South Wales 2065, Australia

ABSTRACT: The study of the early life history of large, open-ocean pelagic fishes such as tunas and billfish, and the identification of spawning and nursery habitats, has been extremely difficult as these animals are intrinsically rare, highly migratory, and difficult to study in captivity. Traditional methods such as the assembling of a developmental series of life stages, or the culturing of unknown eggs and larvae to a point where they can be identified, has not been easy or fruitful for many pelagic species. The discovery of a putative spawning ‘hot spot’ off the Kona coast of Hawaii, coupled with the development of shipboard approaches to real time identification and adaptive sampling of eggs, may provide new approaches and insights into the spawning ecology and reproductive biology of these highly valuable but poorly known species. Here we report the use of a shipboard PCR based assay to differentiate species of istiophorid billfish larvae and identify eggs of istiophorid and xiphiid billfish, coryphaenid dolphinfish, and wahoo. A species-specific multiplex PCR assay was designed to amplify a single, unique size fragment of the mitochondrial cytochrome b gene for all 6 species of Indo-Pacific billfish, both dolphinfish, and the monospecific wahoo. A boiling technique used to extract DNA from larval eye tissue or an individual egg, combined with a single-step PCR assay and agarose electrophoresis, allowed species identification within 3 h of sample acquisition. This nearly real-time identification method for morphologically indistinguishable eggs and larvae provides an opportunity to employ adaptive sampling methods to increase sampling efficiency and will help in determining the spatial and temporal dimensions of spawning and nursery habitats offshore. This study describes the occurrence of blue marlin, dolphinfish, shortbill spearfish, swordfish and wahoo off the Kona coast by molecular approaches, and it provides the first description of the eggs of blue marlin, shortbill spearfish and wahoo.

KEY WORDS: Dolphinfish · Genetic identification · Species-specific PCR · Marlin · Sailfish · Spearfish · Swordfish · Wahoo

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