Skip to main content

Advertisement

Log in

Reproductive biology of wahoo, Acanthocybium solandri, off eastern Australia

  • Research paper
  • Published:
Reviews in Fish Biology and Fisheries Aims and scope Submit manuscript

Abstract

A dearth of basic biological information for wahoo, Acanthocybium solandri, currently hinders the ability of scientists and managers to assess population sustainability and appropriately manage the dramatically increasing global catch. This study examined the gonads of 382 wahoo collected off eastern Australia during 2008–2011 to quantify their reproductive biology in the region. The overall sex ratio of the sample was 3.2:1 (females:males), however this differed significantly among fishing sectors and areas. The estimated fork length at which 50 % of female wahoo reach maturity was 1,046 mm. Similar to the Atlantic Ocean, female wahoo have a protracted summer spawning season during October-February. The mean spawning frequency of female wahoo was uncertain but may be approximately 2–3 days, with evidence of fish actively spawning on consecutive days. Batch fecundity of females was positively correlated with fish size and estimates ranged between 0.65 and 5.12 million oocytes. Relative fecundity was estimated at 122.0 (±9.7) oocytes per gram of ovary free body weight and did not differ with fish size or throughout the spawning season. Estimation of reproductive parameters such as size- and age-at-maturity may facilitate the construction of per-recruit stock assessments of wahoo in the region.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  • Brown-Peterson NJ, Franks JS, Burke AM (2000) Preliminary observations on the reproductive biology of wahoo, Acanthocybium solandri, from the northern Gulf of Mexico and Bimini, Bahamas. Proc Gulf Caribb Fish Inst 51:414–427

    Google Scholar 

  • Chen KS, Crone PR, Hsu CC (2010) Reproductive biology of albacore Thunnus alalunga. J Fish Biol 77:119–136

    Article  PubMed  Google Scholar 

  • Collette BB, Nauen CE (1983) FAO Species catalogue vol. 2 scombrids of the world. FAO fisheries synopsis no. 125, Rome

  • Cooksey CL (1996) Reproductive biology of Spanish mackerel, Scomberomorus maculatus, in the lower Chesapeake Bay. PhD Thesis, The College of William and Mary

  • de Sylva DP, Breder PR (1997) Reproduction, gonad histology, and spawning cycles of North Atlantic billfishes (Istiophoridae). Bull Mar Sci 60:688–697

    Google Scholar 

  • Domeier ML, Speare P (2012) Dispersal of adult black marlin (Istiompax indica) from a Great Barrier Reef spawning aggregation. PLoS ONE 7:e31629

    Article  PubMed  CAS  Google Scholar 

  • FAO (2012) FISHSTAT Plus: Universal software for fishery statistical time series, version 2.3. FAO Fisheries Department, Fishery Information, Data and Statistics Unit

  • Farley JH, Davis TLO (1998) Reproductive dynamics of southern bluefin tuna, Thunnus maccoyii. Fish Bull 96:223–236

    Google Scholar 

  • Farley JH, Williams AJ, Hoyle SD, Davies CR, Clear N, Nicol SJ (in press) Reproductive dynamics and potential annual fecundity of South Pacific albacore tuna (Thunnus alalunga). PLoS One

  • Figuerola-Fernández M, Peña-Alvarado N, Torres-Ruiz W (2008) Maturation and reproductive seasonality of the wahoo (Acanthocybium solandri), red-ear sardine (Harengula humeralis), false pilchard (Harengula clupeola), thread herring (Opisthonema oglinum), crevalle jack (Caranx hippos), horse-eye jack (Caranx latus), blue runner (Caranx crysos), and great barracuda (Sphyraena barracuda) in Puerto Rico. In: Vélez-Arocho J, Diaz-Velázquez E, García-Pérez M, Berrios JM, Rosario-Jiménez A (eds) Aspects of the reproductive biology of recreationally important fish species in Puerto Rico. Department of Natural and Environmental Resources, Fish and Wildlife Bureau

  • Fitzhugh GR, Hettler WF (1995) Temperature influence on postovulatory follicle degeneration in Atlantic menhaden, Brevoortia tyrannus. Fish Bull 93:568–572

    Google Scholar 

  • Hogarth WT (1976) Life history aspects of the wahoo Acanthocybium solandri (Cuvier and Valenciennes) from the coast of North Carolina. PhD Thesis, North Carolina State University

  • Hunter JR, Macewicz BJ (1985a) Measurement of spawning frequency in multiple spawning fishes. NOAA Tech Rep NMFS 36:79–94

    Google Scholar 

  • Hunter JR, Macewicz BJ (1985b) Rates of atresia in the ovary of captive and wild northern anchovy, Engraulis mordax. Fish Bull 83:119–136

    Google Scholar 

  • Hunter JR, Lo NCH, Leong RJH (1985) Batch fecundity in multiple spawning fishes. NOAA Tech Rep NMFS 36:67–77

    Google Scholar 

  • Hunter JR, Macewicz BJ, Sibert JR (1986) The spawning frequency of skipjack tuna, Katsuwonus pelamis, from the south Pacific. Fish Bull 84:895–903

    Google Scholar 

  • Itano DG (2000) The reproductive biology of yellowfin tuna (Thunnus albacares) in Hawaiian waters and the Western Tropical Pacific ocean: project summary. Joint Institute for Marine and Atmospheric Research, Hawaii

  • Jenkins KLM, McBride RS (2009) Reproductive biology of wahoo, Acanthocybium solandri, from the Atlantic coast of Florida and the Bahamas. Mar Freshw Res 60:893–897

    Article  Google Scholar 

  • King MG (2007) Fisheries biology, assessment and management, 2nd edn. Blackwell Publishing Ltd, Oxford

    Book  Google Scholar 

  • Kopf RK, Davie PS, Bromhead DB, Young JW (2012) Reproductive biology and spatiotemporal patterns of spawning in striped marlin Kajikia audax. J Fish Biol 81:1834–1858

    Article  PubMed  CAS  Google Scholar 

  • Mackie M, Lewis P (2001) Assessment of gonad staging systems and other methods used in the study of the reproductive biology of narrow-barred Spanish mackerel, Scomberomorus commerson, in Western Australia. Fish Western Australia Fish Res Rep 136:1–32

    Google Scholar 

  • Mackie MC, Lewis PD, Gaughan DJ, Newman SJ (2005) Variability in spawning frequency and reproductive development of the narrow-barred Spanish mackerel (Scomberomorus commerson) along the west coast of Australia. Fish Bull 103:344–354

    Google Scholar 

  • Massutí E, Morales-Nin M-N (1997) Reproductive biology of dolphin-fish (Coryphaena hippurus L.) off the island of Majorca (western Mediterranean). Fish Res 30:57–65

    Article  Google Scholar 

  • Matsumoto WM (1967) Morphology and distribution of larval wahoo Acanthocybium solandri (Cuvier) in the central Pacific Ocean. Fish Bull 66:299–322

    Google Scholar 

  • McBride RS, Richardson AK, Maki KL (2008) Age, growth and mortality of wahoo, Acantocybium solandri, from the Atlantic coast of Florida and the Bahamas. Mar Freshw Res 59:799–807

    Article  Google Scholar 

  • McPherson GR (1993) Reproductive biology of the narrow barred Spanish Mackerel (Scomberomorus commerson Lacepede, 1800) in Queensland Waters. Asian Fish Sci 6:169–182

    Google Scholar 

  • Queensland Government (2008) Fisheries regulation 2008, reprint 3A. Queensland Government, Brisbane

    Google Scholar 

  • Schaefer KM (1996) Spawning time, frequency, and batch fecundity of yellowfin tuna, Thunnus albacares, near Clipperton Atoll in the eastern Pacific Ocean. Fish Bull 94:98–112

    Google Scholar 

  • Schaefer KM (1998) Reproductive biology of yellowfin tuna (Thunnus albacares) in the Eastern Pacific Ocean. Inter Am Trop Tuna Comm Bull 21:205–272

    Google Scholar 

  • Schaefer KM (2001) Reproductive biology of tunas. Fish Physiol 19:225–270

    Article  Google Scholar 

  • Schaefer KM, Fuller DW, Miyabe N (2005) Reproductive biology of bigeye tuna (Thunnus obesus) in the eastern and central Pacific Ocean. Inter Am Trop Tuna Comm Bull 23:1–31

    Google Scholar 

  • Shimose T, Yokawa K, Saito H, Tachihara K (2012) Sexual difference in the migration pattern of blue marlin, Makaira nigricans, related to spawning and feeding activities in the Western and Central North Pacific Ocean. Bull Mar Sci 88:231–249

    Google Scholar 

  • Shiraishi T, Ketkar SD, Katoh Y, Nyuji M, Yamaguchi A, Matsuyama M (2009) Spawning frequency of the Tsushima current subpopulation of chub mackerel Scomber japonicus off Kyushu, Japan. Fish Sci 75:649–655

    Article  CAS  Google Scholar 

  • van der Velde TD, Griffiths SP, Fry GC (2010) Reproductive biology of the commercially and recreationally important cobia Rachycentron canadum in northeastern Australia. Fish Sci 76:33–43

    Article  CAS  Google Scholar 

  • West G (1990) Methods of assessing ovarian development in fishes: a review. Mar Freshw Res 41:199–222

    Article  Google Scholar 

  • Wollam MB (1969) Larval wahoo, Acanthocybium solanderi, from the straits of Yucatan and Florida. Florida Department Nat Resourc Mar Res Lab Leaflet Ser 4:1–7

    Google Scholar 

  • Young JW, Hobday AJ, Campbell RA, Kloser RJ, Bonham PI, Clementson LA, Lansdell MJ (2011) The biological oceanography of the East Australian Current and surrounding waters in relation to tuna and billfish catches off eastern Australia. Deep Sea Res II 58:720–733

    Article  CAS  Google Scholar 

  • Zhu GP, Dai XJ, Xu LX, Zhou YQ (2010) Reproductive biology of bigeye tuna, Thunnus obesus (Scombridae), in the eastern and central tropical Pacific Ocean. Environ Biol Fish 88:253–260

    Article  Google Scholar 

  • Zischke MT (2012) A review of the biology, stock structure, fisheries and status of wahoo (Acanthocybium solandri), with reference to the Pacific Ocean. Fish Res 119–120:13–22

    Article  Google Scholar 

  • Zischke MT, Griffiths SP, Tibbetts IR (2012) Catch and effort from a specialised recreational pelagic sport fishery off eastern Australia. Fish Res 127–128:61–72

    Article  Google Scholar 

  • Zischke MT, Griffiths SP, Tibbetts IR, Lester RJG (2013) Stock identification of wahoo (Acanthocybium solandri) in the Pacific and Indian Oceans using morphometrics and parasites. ICES J Mar Sci 70:164–172

    Article  Google Scholar 

  • Zischke MT, Griffiths SP, Tibbetts IR (in press) Rapid growth of wahoo (Acanthocybium solandri) in the Coral Sea, based on length-at-age estimates using annual and daily increments on sagittal otoliths. ICES J Mar Sci

Download references

Acknowledgments

We thank the numerous commercial, charter and recreational fishers that donated samples for this research. We also thank S. Hall, W. Hagedoorn, J. Cavallaro, B. Lamason and G. Heilmann for assisting with the logistics of sample collection, storage and freight. B. Gilby, B. Lockett, J. Lerner, M. O’Haire, N. Silvana Santini González and A. Heemsoth assisted with laboratory dissections. T. van der Velde is thanked for assistance with histological procedures. This research was funded by the Winifred Violet Scott Estate and an Ethel Mary Reid grant from the Royal Zoological Society of NSW. M.T.Z was funded by a University of Queensland Research Scholarship, with support provided by CSIRO Division of Marine and Atmospheric Research. This research was approved by The University of Queensland Animal Ethics Committee (approval number CMS/884/08/FRDC/URG).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mitchell T. Zischke.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zischke, M.T., Farley, J.H., Griffiths, S.P. et al. Reproductive biology of wahoo, Acanthocybium solandri, off eastern Australia. Rev Fish Biol Fisheries 23, 491–506 (2013). https://doi.org/10.1007/s11160-013-9304-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11160-013-9304-z

Keywords

Navigation