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RESEARCH ARTICLE
Contents Vol 56(7)

Age and growth of larval Atlantic sailfish, Istiophorus platypterus

Stacy A. Luthy A C D , Joseph E. Serafy B , Robert K. Cowen A , Kelly L. Denit A and Su Sponaugle A
+ Author Affiliations
- Author Affiliations

A Division of Marine Biology and Fisheries, Rosenstiel School of Marine and Atmospheric Science, University of Miami, 4600 Rickenbacker Causeway, Miami, FL 33149, USA.

B National Marine Fisheries Service, Southeast Fisheries Science Center, 75 Virginia Beach Drive, Miami, FL 33149, USA.

C Present address: Baruch Marine Field Laboratory, PO Box 1630, Georgetown, SC 29442, USA.

D Corresponding author. Email: stacy@belle.baruch.sc.edu

Marine and Freshwater Research 56(7) 1027-1035 https://doi.org/10.1071/MF05048
Submitted: 4 March 2005  Accepted: 20 June 2005   Published: 3 November 2005

Abstract

Of the Atlantic istiophorid billfishes, larval age–size relationships and growth rates have been examined only for blue marlin (Makaira nigricans). Using otolith microincrement analysis, we describe age–length and age–weight relationships for larval sailfish (Istiophorus platypterus) collected from the Straits of Florida. Sagittae and lapilli were dissected from 70 larvae ranging from 2.8 to 15.2 mm in (notochord or standard) length. Comparisons between otolith images obtained by light microscopy and scanning electron microscopy indicated that increment widths were well within the resolving power of light microscopy. Indirect evidence and published descriptions of larval blue marlin otoliths suggest daily increment deposition. Estimated ages of specimens ranged from 3 to 18 days. Length data were fitted to age estimates with an exponential model (R2 = 0.85). The estimated size-at-hatch for sailfish was 1.96 mm notochord length, and the daily instantaneous growth coefficient was 0.14. A power curve with exponent 3.05 described the length–dry weight relationship for sailfish. The instantaneous growth coefficient for an exponential regression of dry weight, converted from length, versus estimated age was 0.41. Growth in the length of sailfish larvae from the Straits of Florida was very similar to that described for blue marlin larvae from Exuma Sound, Bahamas.

Extra keywords: billfish, Istiophoridae, otoliths, sagitta, weight–length relationship.


Acknowledgments

Financial support was provided by the University of Miami Maytag fellowship, Network Miami, Anheuser Busch, the American Institute of Marine Science, the Yamaha Miami Billfish tournament (Harry Vernon Jr. Memorial Scholarship), the International Light Tackle Tournament Association and the Sportfishermen of Broward. Collection of the larvae was made possible by the generosity and efforts of the Frazel family and by the hard work of collection volunteers G. Diaz, G. Myers, K. Gracie, L. Leist, M. Williams, O. Bowen, C. Schmitz, C. Faunce, D. Schuller, T. Capo and M. Feeley. We thank M. Lynn, P. Blackwelder and B. Elkind of the University of Miami electron microscopy lab. We appreciate expert otolith dissection instruction by J. Fortuna.


References

Alvarado-Castillo, R. M. , and Félix-Uraga, R. (1996). Age determination in Istiophorus platypterus (Pisces: Istiophoridae) in the south of the Gulf of California, Mexico. Revista de Biologia Tropical 44, 233–239.
Anderson J. T. (1988). A review of size dependent survival during pre-recruit stages of fishes in relation to recruitment. Journal of Northwest Atlantic Fishery Science 8, 55–66.

Benetti, D. D. (1992). Bioenergetics and growth of dolphin, Coryphaena hippurus. Ph.D. Thesis, University of Miami, Miami, FL.

Bolz, G. R. , and Lough, R. G. (1983). Growth of larval Atlantic cod, Gadus morhua, and haddock, Melanogrammus aeglefinus, on Georges Bank, Spring 1981. Fishery Bulletin 81, 827–836.
Brothers E. B. (1979). Age and growth studies on tropical fishes. In ‘Stock Assessment for Tropical Small-Scale Fisheries: Proceedings of an International Workshop Held at the University of Rhode Island, Kingston, RI. 19–21 Sept. 1979’. (Eds S. B. Saila and P. M. Roedel.) pp. 119–136. (International Center for Marine Resources Development, University of Rhode Island: Kingston, RI.)

Brothers, E. B. , Mathews, C. , and Lasker, R. (1976). Daily growth increments in otoliths from larval and adult fishes. Fishery Bulletin 74, 1–8.
Campana S. E. (1992). Measurement and interpretation of the microstructure of fish otoliths. In ‘Otolith Microstructure Examination and Analysis’. (Eds D. K. Stevenson and S. E. Campana.) pp. 59–71. (Canadian Special Publication of Fisheries and Aquatic Sciences 117.)

de Sylva, D. P. (1957). Studies on the age and growth of the Atlantic sailfish, Istiophorus americanus (Cuvier), using length-frequency curves. Bulletin of Marine Science of the Gulf and Caribbean 7, 1–20.
Hedgepeth M. Y., and Jolley J. W. (1983). Age and growth of sailfish, Istiophorus platypterus, using cross sections from the fourth dorsal fin spine. In ‘Proceedings of the International Workshop on Age Determination of Oceanic Pelagic Fishes: Tunas, Billfishes, and Sharks’. (Eds E. D. Prince and L. M. Pulos.) pp. 131–135. (NOAA Technical Report 8.)

Houde, E. D. (1989). Comparative growth, mortality, and energetics of marine fish larvae – temperature and implied latitudinal effects. Fishery Bulletin 87, 471–495.
Jolley J. W. (1974). On the biology of Florida east coast Atlantic sailfish (Istiophorus platypterus). In ‘Proceedings of the International Billfish Symposium, Kailua-Kona, Hawaii. 9–12 August 1972. Part 2. Review and Contributed Papers’. (Eds R. S. Shomura and F. Williams.) pp. 81–88. (NOAA Technical Report NMFS SSRF-675.)

Jolley J. W. (1977). ‘The Biology and Fishery of Atlantic Sailfish Istiophorus platypterus, from Southeast Florida.’ (Florida Marine Research Publication, 28: St. Petersburg, FL.)

Jones, C. , and Brothers, E. B. (1987). Validation of the otolith increment aging technique for striped bass, Morone saxatilis, larvae reared under suboptimal feeding conditions. Fishery Bulletin 85, 171–178.
Jones C. M. (2002). Age and growth. In ‘Fishery Science: The Unique Contributions of Early Life Stages’. (Eds L. A. Fuiman and R. G. Werner.) pp. 33–63. (Blackwell: Oxford.)

Juanes, F. , and Conover, D. O. (1994). Rapid growth, high feeding rates, and early piscivory in young-of-the-year bluefish (Pomatomus saltatrix). Canadian Journal of Fisheries and Aquatic Sciences 51, 1752–1761.
Neilson J. D. (1992). Sources of error in otolith microstructure examination. In ‘Otolith Microstructure Examination and Analysis’. (Eds D. K. Stevenson and S. E. Campana.) pp. 115–126. (Canadian Special Publication of Fisheries and Aquatic Sciences 117.)

Neilson, J. D. , and Geen, G. H. (1982). Otoliths of chinook salmon (Oncorhynchus tshawytscha): daily growth increments and factors influencing their production. Canadian Journal of Fisheries and Aquatic Sciences 39, 1340–1347.
Radtke R. L. (1983). Otolith formation and increment deposition in laboratory-reared skipjack tuna, Euthynnus pelamis, larvae. In ‘Proceedings of the International Workshop on Age Determination of Oceanic Pelagic Fishes: Tunas, Billfishes, and Sharks’. (Eds E. D. Prince and L. M. Pulos.) pp. 99–103. (NOAA Technical Report NMFS-8.)

Radtke, R. L. , and Dean, J. M. (1981). Morphological features of the otoliths of the sailfish, Istiophorus platypterus, useful in age determination. Fishery Bulletin 79, 360–367.
Secor D. H., Dean J. M., and Laban E. H. (1992). Otolith removal and preparation for microstructural examination. In ‘Otolith Microstructure Examination and Analysis’. (Eds D. K. Stevenson and S. E. Campana.) pp. 19–57. (Canadian Special Publication of Fisheries and Aquatic Sciences 117.)

Serafy, J. E. , Cowen, R. K. , Paris, C. B. , Capo, T. R. , and Luthy, S. A. (2003). Evidence of blue marlin, Makaira nigricans, spawning in the vicinity of Exuma Sound, Bahamas. Marine and Freshwater Research 54, 299–306.
| Crossref | GoogleScholarGoogle Scholar | Tanaka M., Kaji T., Nakamura Y., and Takahashi Y. (1996). Developmental strategy of scombrid larvae: high growth potential related to food habits and precocious digestive system development. In ‘Survival Strategies in Early Life Stages of Marine Resources’. (Eds Y. Watanabe, Y. Yamashita and Y. Oozeki.) pp. 125–139. (Balkema Publishers: Brookfield, VT.)

Ueyanagi, S. (1974). Some considerations on the early life stage of the sailfish, Istiophorus platypterus, particularly regarding the transport of larvae by surface currents. Bulletin of the Far Seas Fisheries Research Laboratory 10, 189–191.


Warlen, S. M. , and Chester, A. J. (1985). Age, growth, and distribution of larval spot, Leiostomus xanthurus, off North-Carolina. Fishery Bulletin 83, 587–599.


Yasuda, F. , Kohno, H. , Yatsu, A. , Ida, H. , Arena, P. , Greci, F. L. , and Taki, Y. (1978). Embryonic and early larval stages of the swordfish, Xiphias gladius, from the Mediterranean. Journal of the Tokyo University of Fisheries 65, 91–97.