Maturation of female common snook <i>Centropomus undecimalis</i>: implications for managing protandrous fishes

Journal of Fish Biology - Tập 97 Số 5 - Trang 1317-1331 - 2020
Joy Young1, Beau G. Yeiser2, James A. Whittington1, Jynessa Dutka‐Gianelli3
1Florida Fish and Wildlife Conservation Commission, Fish and Wildlife Research Institute, Tequesta Field Laboratory, Tequesta, Florida, USA
2Florida Fish and Wildlife Conservation Commission, South Regional Office, West Palm Beach, Florida, USA
3Gloucester Marine Station, University of Massachusetts Amherst, Gloucester, Massachusetts, USA

Tóm tắt

AbstractThe assumption for hermaphroditic fish species that mature individuals of the terminal sex arise directly from mature individuals of the primary sex has led to the use of sex ratios as a proxy for age at maturity (A50). The timing of transition and deficient energy reserves, however, can result in a delay between transition and spawning. To test the assumption of female maturity and investigate the relationship between maturation and energy reserves, common snook, Centropomus undecimalis, a protandrous hermaphrodite, were collected from rivers, estuaries, inlets and offshore habitats on the east coast of Florida during 2010–2015. Immature females were observed every month, with lowest proportions during the peak spawning months of July and August. When calculated based on sex ratio, A50 (8.1 years) overestimated the age at which 50% of the female population was, in fact, mature (4.1–4.9 years). Best‐fit models indicate that mesenteric fat index (IF) and hepato‐somatic index (IH) were significantly affected by gonad phase, month and size and weakly by habitat. In post hoc analysis, immature female IF did not differ significantly from developing and regenerating females, but immature female IH was significantly lower than that for all mature phases except animals in the regressing phase. Although immature females may have sufficient energy in terms of fat, it appears that energy is not allocated to reproductive processes, as evidenced by lower IH. Nonetheless, approximately 95% of females were spawning‐capable during peak spawning months, suggesting that the energy threshold at which immature females reach maturity is met by most females each spawning cycle.

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Tài liệu tham khảo

10.1111/faf.12442

10.1080/19425120.2011.556927

Alonzo S. H., 2004, Status of the California sheephead (Semicossyphus pulcher) stock (2004)

Alonzo S. H., 2005, Sex‐change rules, stock dynamics, and the performance of spawning‐per‐recruit measures in protogynous stocks, Fishery Bulletin, 103, 229

10.1139/f01-015

Bentivegna F., 1983, Anatomical features of sex inversion in the rainbow wrasse, Coris julis, Bollettino di zoologia, 50, 73, 10.1080/11250008309439424

10.1023/A:1023332216713

Blewett D. A., 2013, Comparative ecology of euryhaline and freshwater predators in a subtropical floodplain river, Florida Scientist, 76, 166

10.1007/s00442-004-1608-1

10.3354/ab00679

10.1111/j.1095-8649.2000.tb02105.x

Brooks E. N., 2008, Stock assessment of protogynous fish: evaluating measures of spawning biomass used to estimate biological reference points, Fishery Bulletin, 106, 12

Brown‐Peterson N. J., 2011, A standardized terminology for describing reproductive development in fishes. Marine and Coastal Fisheries: Dynamics, Management and Ecosystem Science, 3, 52

10.1095/biolreprod.111.094730

10.1080/01650521.2019.1663594

Dutka‐Gianelli J., 2011, Habitat utilization and resource partitioning of apex predators in coastal rivers of Southeast Florida. FWRI library no.: F2771‐07‐11‐F

10.1007/s10641-007-9246-1

Florida Fish and Wildlife Conservation Commission. (2019).The economic impacts of saltwater fishing in Florida.https://myfwc.com/conservation/value/saltwater-fishing/

10.1016/j.fishres.2008.01.005

Gassman J., 2017, Reproduction of Centropomus undecimalis and C. ensiferus (Perciformes: Centropomidae) in a tropical coastal lagoon, Revista de Biologia Tropical, 65, 181, 10.15517/rbt.v65i1.23614

Gilmore R. G., 1983, Observations on the distribution and biology of east‐Central Florida populations of the common Snook, Centropomus undecimalis (Bloch), Florida Scientist, 46, 313

10.1111/j.1469-7998.1994.tb01569.x

10.1007/BF00005126

10.1023/B:EBFI.0000033344.21383.00

Hunter J. R., 2003, Report of the working group on modern approaches to assess maturity and fecundity of warm‐ and cold‐water fish and squids

10.1111/j.1095-8649.1999.tb00716.x

10.1016/0044-8486(96)01258-6

10.3989/scimar.2005.69n3391

10.1016/0044-8486(94)00399-9

10.1016/S1385-1101(98)00029-X

10.1111/jfb.12765

10.1111/j.1095-8649.2001.tb02294.x

10.1111/jfb.13331

Lowerre‐Barbieri S. K., 1993, A new method of oocyte separation and preservation for fish reproduction studies, Fishery Bulletin, 91, 165

10.1080/19425120.2011.556932

10.1111/j.1365-2109.2005.01253.x

10.1016/j.aquaculture.2012.08.012

10.1139/f04-128

10.1002/jez.1402720105

10.1111/faf.12043

Myers R. A., 1996, Is fish recruitment related to spawner abundance?, Fishery Bulletin, 94, 707

10.1016/j.fishres.2012.02.019

Muller R. G. Trotter A. A. &Stevens P. W.(2015). The 2015 stock assessment update of common Snook Centropomus undecimalis. In House report: IHR 2015–004. Florida Fish and Wildlife Conservation Commission St. Petersburg FL.

10.1051/alr:1989018

Novoa‐Pabon A. Barros P. Krug H. Silva P. &Pinho M. R.(2015). Yield per recruit analysis for the red blackspot seabream (Pagellus bogaraveo) stock from the Azores. ICES CM 2015/A 33.

10.1016/S1385-1101(02)00135-1

10.1111/are.12565

10.1080/03632415.2015.1093471

10.3109/10520299109109964

10.1080/00028487.2013.788564

10.1016/j.icesjms.2006.04.014

10.2307/1444940

10.1016/j.fishres.2019.03.013

10.1016/0044-8486(90)90121-3

10.1016/j.seares.2014.05.003

10.1111/j.1467-2979.2007.00266.x

Schaefer K. M., 1996, Spawning time, frequency, and batch fecundity of yellowfin tuna, Thunnus albacares, near Clipperton atoll in the eastern Pacific Ocean, Fishery Bulletin, 94, 98

Seaman W. &Collins M.1983.Species profiles: life histories and environmental requirements of coastal fishes and invertebrates (south Florida): Snook. U.S. Fish and Wildlife Service FWS/OBS‐82/11.16. U.S. Army Corps of Engineers TR EL‐82‐4.

10.1577/T07-105.1

SEDAR, 2012, SEDAR 01‐ update stock assessment of South Atlantic red porgy

SEDAR, 2013, SEDAR 36‐ stock assessment report: South Atlantic snowy grouper

SEDAR, 2014, SEDAR 33‐ stock assessment report: Gulf of Mexico gag grouper

SEDAR, 2015, SEDAR 42‐ final stock assessment report: Gulf of Mexico red grouper

SEDAR, 2017, SEDAR 37‐ update, SEDAR 37 Gulf of Mexico hogfish

10.1016/j.fishres.2008.03.006

10.1007/s12237-019-00650-x

10.1016/j.ygcen.2009.05.004

10.1111/j.1095-8649.1998.tb00998.x

Taylor R. G., 2000, Age, growth, maturation, and protandric sex reversal in common Snook, Centropomus undecimalis, from the east and west coasts of South Florida, Fishery Bulletin, 98, 612

Thomas S. M., 2019, The annual reproductive cycle and sex inversion of the picnic seabream, Acanthopagrus berda (Forsskål 1775) from Indian waters: histological and morphometric description, Aquaculture Research, 50, 2917, 10.1111/are.14246

10.1023/A:1022351814644

10.1016/j.ygcen.2014.04.033

10.1080/00028487.2012.675903

Tucker J. W., 1988, Spawning season of common Snook along the east Central Florida coast, Florida Scientist, 51, 1

10.1071/MF12362

10.2307/1542090

10.1071/MF9900199

10.1006/jmsc.1999.0522

10.1577/T08-215.1

10.1016/j.icesjms.2005.04.018

10.3354/meps10774

10.1080/00028487.2015.1131741