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Marine and Freshwater Research Marine and Freshwater Research Society
Advances in the aquatic sciences
RESEARCH ARTICLE

Age, growth, and mortality of wahoo, Acanthocybium solandri, from the Atlantic coast of Florida and the Bahamas

Richard S. McBride A , Adam K. Richardson A and Kristin L. Maki A B C
+ Author Affiliations
- Author Affiliations

A Florida Fish and Wildlife Conservation Commission, 100 8th Avenue SE, St. Petersburg, FL 33701, USA.

B Present address: PBS&J, 5300 W. Cypress, Tampa, FL 33607, USA.

C Corresponding author. Email: klmaki@pbsj.com

Marine and Freshwater Research 59(9) 799-807 https://doi.org/10.1071/MF08021
Submitted: 30 January 2008  Accepted: 29 June 2008   Published: 7 October 2008

Abstract

Wahoo, Acanthocybium solandri, constitute an economically important fishery for many coastal nations, but assessment of this living marine resource is hampered by a lack of basic life history information. The present study demonstrates that wahoo in the western North Atlantic Ocean are short lived, grow rapidly in their first year, achieve a very large size, and have high mortality rates. The largest individuals were female and the sex ratio was significantly female-biased (298 females: 223 males: 54 unknown sex). An edge analysis showed that annuli formed primarily during winter–spring, which supported the use of sectioned otoliths for ageing wahoo. Wahoo lived a median of 1.3 years, a mean of 1.8 years, and a maximum of 9.3 years (n = 469). They had a high instantaneous mortality rate (Z = 0.98), and they grew rapidly and to a large size; von Bertalanffy growth parameters were: L = 1701 mm fork length (FL), K = 0.381, to = –1.63. Females had a very similar maximum age relative to males (maximum age 9.3 v. age 9.1 years), and they had a slightly, but not significantly, lower mortality (Z = 0.91 v. 1.1) than males. Females grew slightly, although not significantly, larger than males (L = 1797 v. 1555 mm FL, maximum observed = 1804 v. 1585 mm FL). Presumably the piscivorous nature of wahoo feeding, as noted by others, fuels these fast growth rates. Comparative data are very limited but it appears that the survival rate of wahoo in the western Atlantic Ocean is not different now than in the 1960s.

Additional keywords: age, mortality, sexual dimorphism, von Bertalanffy growth.


Acknowledgements

We are grateful to the many anglers who donated their fish and to the organisers of the following fishing tournaments for arranging access to fish: the Bahamas Wahoo Championship; the Boldwater Dolphin/Wahoo Slamathons; the Cal Dixon Celebrity Offshore Fishing Classic; the Coconuts on the Beach Wahoo and Dolphin Shootout; the Ed Dwyer Other Side Invitational; the Fin’s Fall Offshore Classic; the Fishin’ Cove Offshore Shootout; the Fishin’ Store Slams; the Fishstock Tournament; the Florida Sport Fishing Association’s Offshore Slam; the Fort Pierce Open; the Halifax Sportfishing Club Offshore Challenge; the H.O.T. Circuit Tournament Series; the Indian River County Sheriff’s Blue Water Tournament; the Palm Beach County KDW Classic; the Sebastian Inlet Blue Water Open & Spring Fling; and the Treasure Coast Builders Association Tournaments. Valuable supplemental samples were provided by the many samplers of the FWC Fisheries-Dependent Monitoring program, particularly J. Digennaro, K. Kowal, D. McGowan, and E. Sander. D. Adams (FWC), J. Baldwin (Florida Atlantic University (FAU)), G. Haddle (NOAA Fisheries), and T. Theisen (FAU) provided even more samples, and carcasses were obtained with the helpful assistance of Lott Bros., Fishing Headquarters, Finest Kind Marina, Sailfish Marina, M. Legakis, and the local fishing community. J. Tunnell (FWC) assisted with reading otoliths. This research was funded by a MARFIN Award (# NA17FF2882) from the National Oceanic and Atmospheric Administration, USA Department of Commerce. The statements, finding, conclusions, and recommendations are those of the authors and do not necessarily reflect the views of the National Oceanic and Atmospheric Administration or the Department of Commerce.


References

Beardsley, G. L. , and Richards, W. J. (1970). Size, seasonal abundance, and length-weight relation of some scombrid fishes from southeast Florida. United States. Fish & Wildlife Service Special Scientific Report Fisheries 595, 1–6.
Collette B. B. (2002). Scombridae. In ‘The Living Marine Resources of the Western Central Atlantic. Volume 2: Bony Fishes Part 2 (Opistognathidae to Molidae), Sea Turtles and Marine Mammals. FAO Species Identification Guide for Fishery Purposes and American Society of Ichthyologists and Herpetologists Special Publication No. 5’. (Ed. K. E. Carpenter.) pp. 1701–1722. (Food Agricultural Organization: Rome.)

Franks J. S., Brown-Peterson N. J., Griggs M. S., Garber N. M., Warren J. R., and Larsen K. M. (2000). Potential of the first dorsal fin spine for estimating the age of wahoo, Acanthocybium solandri, from the northern Gulf of Mexico, with comments on specimens from Bimini, Bahamas. In ‘Proceedings of the Gulf and Caribbean Fisheries Institute 51st Annual Meeting, St. Croix, USVI’, pp. 428–440.

Franks J. S., Shea J. L., Brown-Peterson N. J., Griggs M. S., and Larsen K. M. (2001). Attempts to enhance the visibility and contrast of presumed growth marks on sagittal otoliths from wahoo, Acanthocybium solandri, from the northern Gulf of Mexico and Bimini, Bahamas. In ‘Proceedings of the Gulf and Caribbean Fisheries Institute 52nd Annual Meeting, Key West, FL’, pp. 577–585. (Gulf and Caribbean Fisheries Institute: Marathon, FL, USA.)

Garber, A. F. , Tringali, M. D. , and Franks, J. S. (2005). Population genetic and phylogeographic structure of wahoo, Acanthocybium solandri, from the western Atlantic and central Pacific Oceans. Marine Biology (Berlin) 147, 205–214.
Crossref | GoogleScholarGoogle Scholar | Hogarth W. T. (1976). Life history aspects of the wahoo Acanthocybium solandri (Cuvier and Valenciennes) from the coast of North Carolina. PhD Dissertation. North Carolina State University, Raleigh, NC, USA.

Johnson, J. C. , Griffith, D. C. , and Murray, J. D. (1987). Encouraging the use of underutilized marine fishes by southeastern U.S. anglers, Part I: The research. Marine Fisheries Review 49, 122–137.
Kishore R., and Chin X. (2001). Age and growth studies at the CFRAMP/IMA Regional Age and Growth Laboratory – progress of work done and future approaches. In ‘Report of the 2000 Caribbean Pelagic and Reef Fisheries Assessment and Management Workshop. June 5–7, 2000’. (Ed. S. Singh-Renton.) pp. 74–89. (CARICOM Fishery Report 9: Hasing, Barbados.)

Luckhurst B. E., and Trott T. (2000). Bermuda’s commercial line fishery for wahoo and dolphinfish: landings, seasonality and catch per unit effort trends. In ‘Proceedings of the Gulf and Caribbean Fisheries Institute 51st Annual Meeting, St. Croix, USVI’, pp. 404–413. (Gulf and Caribbean Fisheries Institute: Marathon, FL, USA.)

Luckhurst B. E., Dean J. M., Reichert M., Carmeron M., Manuel S., and Trott T. (1997). Use of microstructure analysis of the sagittal otoliths for age estimation of the wahoo, Acanthocybium solandri, from Bermuda. In ‘Proceedings of the Gulf and Caribbean Fisheries Institute 49th Annual Meeting, Christ Church, Barbados’, pp. 64–70. (Gulf and Caribbean Fisheries Institute: Marathon, FL, USA.)

McBride R. S., Richardson A. K., Maki K. L., and Murphy M. D. (2007). Fishery and population characteristics of wahoo, Acanthocybium solandri, in Florida and adjacent waters of the western North Atlantic Ocean. Final Report. Marine Fisheries Initiative Grant Program. NOAA Award Number NA17FF2882. Prepared for U.S. Department of Commerce, NOAA, NMFS, Cooperative Program Division, St. Petersburg, FL, USA.

Murray P. A., and Joseph W. B. (1997). Trends in the exploitation of the wahoo, Acanthocybium solandri, by the St. Lucian pelagic fishery. In ‘Proceedings of the 44th Gulf and Caribbean Fisheries Institute’, pp. 737–746. (Gulf and Caribbean Fisheries Institute: Marathon, FL, USA.)

Nash, A. , Whiting, J. , and Luckhurst, B. E. (2002). A pneumatic cradle for handling and tagging of wahoo and other large pelagic fishes. Catch and release in marine recreational fisheries. American Fisheries Society Symposium 30, 189–194.
Neilson J. D., Murray P. A., Finlay J. A., and Rennie J. (1999). Wahoo landings in the Lesser Antilles: biased samples cause problems for stock assessment. In ‘Proceedings of the 46th Gulf and Caribbean Fisheries Institute’, pp. 346–359. (South Atlantic Fishery Management Council: Charleston, SC.)

Oxenford, H. A. , Murray, P. A. , and Luckhurst, B. E. (2003). The biology of wahoo (Acanthocybium solandri) in the western central Atlantic. Gulf and Caribbean Research 15, 33–49.
South Atlantic Fishery Management Council (2003). Fishery Management Plan for the Dolphin and Wahoo Fishery of the Atlantic, Caribbean, and Gulf of Mexico. South Atlantic Fishery Management Council, Charleston, SC, USA. Available at http://www.safmc.net/Portals/6/Library/FMP/DolphinWahoo/DolphinWahooFMP.pdf. [Accessed 3 September 2008.]

SAS Institute (1999). ‘SAS/STAT User’s Guide.’ Version 8. Volumes I–III. (SAS Institute Inc.: Cary, North Carolina).

Schwenke, K. L. , and Buckel, J. A. (2008). Age, growth, and reproduction of dolphinfish (Coryphaena hippurus) caught off the coast of North Carolina. Fishery Bulletin 106, 82–92.
Theisen T. C. (2007). Population genetic structure, movement patterns, and environmental preferences of the pelagic wahoo, Acanthocybium solandri. PhD Dissertation. Florida Atlantic University, Department of Biology, Boca Raton, FL, USA.

Theisen T. C., Bowen B. W., Lanier W., and Baldwin J. D. (2008). High connectivity on a global scale in the pelagic wahoo, Acanthocybium solandri (tuna family Scombridae). Molecular Ecology 17, 4233–4247.

VanderKooy S., and Guindon-Tisdel K. (2003). A Practical Handbook for Determining the Ages of Gulf of Mexico Fishes. GSMFC Pub. No. 111. Gulf States Marine Fisheries Commission, Ocean Springs, MS. Available at http://www.gsmfc.org/publications/GSMFC%20Number%20111.pdf. [Accessed 7 September 2008.]