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Reproductive biology of the marine ornamental shrimp Lysmata boggessi in the south-eastern Gulf of Mexico

Published online by Cambridge University Press:  04 September 2013

J. Antonio Baeza ,
Donald C. Behringer ,
Rebecca J. Hart ,
Michael D. Dickson  and
Joshua R. Anderson
J. Antonio Baeza*
Affiliation:
Smithsonian Marine Station at Fort Pierce, 701 Seaway Drive, Fort Pierce, FL 34949, USA Universidad Catolica del Norte, Larrondo 1281, Coquimbo, Chile
Donald C. Behringer
Affiliation:
School of Forest Resources and Conservation, Fisheries and Aquatic Sciences Program, University of Florida, Gainesville, FL 32653, USA Emerging Pathogens Institute, University of Florida, Gainesville, FL 32611, USA
Rebecca J. Hart
Affiliation:
School of Forest Resources and Conservation, Fisheries and Aquatic Sciences Program, University of Florida, Gainesville, FL 32653, USA
Michael D. Dickson
Affiliation:
School of Forest Resources and Conservation, Fisheries and Aquatic Sciences Program, University of Florida, Gainesville, FL 32653, USA
Joshua R. Anderson
Affiliation:
School of Forest Resources and Conservation, Fisheries and Aquatic Sciences Program, University of Florida, Gainesville, FL 32653, USA
*
Correspondence should be addressed to: J. Antonio Baeza, Department of Biological Sciences, Clemson University Clemson, South Carolina, USA email: [email protected].
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Abstract

Reproductive aspects of the intensively traded ornamental shrimp Lysmata boggessi were examined. Abundance, reproductive biology (fecundity, reproductive output and egg size) and population structure (frequency distribution, size at sex phase change and sex phase ratio) were examined at three different fishing grounds off south and west-central Florida between May 2011 and February 2012. Fishery-dependent densities of L. boggessi varied between 2.51 ± 1.39 and 13.05 ± 9.30 shrimps per 1000 m2 at two different localities. The proportion of brooding shrimp varied considerably at one locality during two different dates, suggesting reproductive seasonality. Reproductive output increased linearly with shrimp body weight (SBW) at one locality (May 2011), but scaled negatively with SBW at a second locality (January–February 2012). Lastly, no correlation between embryo size and shrimp carapace length (CL) was recorded at one locality (May 2011), but a slight negative correlation between embryo size and CL was found at the second locality (January–February 2012). Lysmata boggessi might be experiencing trade-offs between different reproductive parameters driven by environmental, probably seasonal, conditions during the year. All of this information needs to be considered in assessing shrimp stocks and establishing a sustainable management plan.

Keywords

sex-ratiodensitysize at first maturityaquarium tradehermaphrodite
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 94 , Issue 1 , February 2014 , pp. 141 - 149
Copyright
Copyright © Marine Biological Association of the United Kingdom 2013 

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References

REFERENCES

Baeza, J.A. (2006) Testing three models on the adaptive significance of protandric simultaneous hermaphroditism in a marine shrimp. Evolution 60, 1840–1850.Google Scholar
Baeza, J.A. (2007) Sex allocation in a simultaneously hermaphroditic marine shrimp. Evolution 61, 2360–2373.CrossRefGoogle Scholar
Baeza, J.A. (2009) Protandric simultaneous hermaphroditism is a conserved trait in Lysmata (Caridea: Lysmatidae): implications for the evolution of hermaphroditism in the genus. Smithsonian Contributions to Marine Science 38, 95–110.Google Scholar
Baeza, J.A. (2010) The symbiotic lifestyle and its evolutionary consequences: social monogamy and sex allocation in the hermaphroditic shrimp Lysmata pederseni. Naturwissenschaften 97, 729–741.CrossRefGoogle ScholarPubMed
Baeza, J.A. (2013) Multi-locus molecular phylogeny of broken-back shrimps (genus Lysmata and allies): a test of the ‘Tomlinson–Ghiselin' hypothesis explaining the evolution of hermaphroditism. Molecular Evolution and Phylogenetics 69, 46–62.CrossRefGoogle Scholar
Baeza, J.A. and Bauer, R.T. (2004) Experimental test of social mediation of sex change in a protandric sequential hermaphrodite; the marine shrimp Lysmata wurdemanni (Crustacea: Caridea). Behavioral Ecology and Sociobiology 55, 544–550.Google Scholar
Baeza, J.A., Braga, A.A., López-Greco, L.S., Perez, E., Negreiros-Fransozo, M.L. and Fransozo, A. (2010) Population dynamics, sex ratio and size at sex change in a protandric–simultaneous hermaphrodite, the spiny shrimp Exhippolysmata oplophoroides. Marine Biology 157, 2643–2653.CrossRefGoogle Scholar
Baeza, J.A., Reitz, J. and Collin, R. (2007) Protandric simultaneous hermaphroditism and sex ratio in the shrimp Lysmata nayaritensis. Journal of Natural History 41, 2843–2850.CrossRefGoogle Scholar
Baeza, J.A. and Thiel, M. (2000) Host use pattern and life history of Liopetrolisthes mitra, an associate of the black sea urchin Tetrapygus niger. Journal of the Marine Biological Association of the United Kingdom 80, 39–45.CrossRefGoogle Scholar
Bauer, R.T. (2004) Remarkable shrimps: natural history and adaptations of the Carideans. 1st edition.Norman, OK: University of Oklahoma Press.Google Scholar
Bauer, R.T. and Holt, G.J. (1998) Simultaneous hermaphroditism in the marine shrimp Lysmata wurdemanni (Caridea: Hippolytidae): an undescribed sexual system in the decapod Crustacea. Marine Biology 132, 223–235.CrossRefGoogle Scholar
Bruckner, A.W. (2005) The importance of the marine ornamental reef fish trade in the wider Caribbean. Revista de Biologia Tropical 53(S1), 127–138.Google ScholarPubMed
Calado, R. (2008) Marine ornamental shrimp: biology, aquaculture and conservation. 1st edition.London: Wiley & Blackwell.Google Scholar
Calado, R., Lin, J., Rhyne, A.L., Araújo, R. and Narciso, L. (2003) Marine ornamental decapods—popular, pricey, and poorly studied. Journal of Crustacean Biology 23, 963–973.CrossRefGoogle Scholar
Chapman, F.A., Fitz-Coy, S.A., Thunberg, E.M. and Adams, C.M. (1997) United States of America trade in ornamental fish. Journal of the World Aquaculture Society 28, 1–10.CrossRefGoogle Scholar
Charnov, E.L. (1982) The theory of sex allocation. 1st edition.Princeton, NJ: Princeton University Press.Google ScholarPubMed
Fiedler, G.C. (1998) Functional, simultaneous hermaphroditism in female-phase Lysmata amboinensis (Decapoda: Caridea: Hippolytidae). Pacific Science 52, 161–169.Google Scholar
France, K.E. and Duffy, J.E. (2006) Biodiversity, dispersal, and scale interactively affect stability of ecosystem function in seagrass metacommunities. Nature 441, 1139–1143.CrossRefGoogle Scholar
Friedlander, A.M. (2001) Essential fish habitat and the effective design of marine reserves: application for marine ornamental fishes. Aquarium Sciences and Conservation 3, 135–150.CrossRefGoogle Scholar
Hartnoll, R.G. (1982) Growth. In Abele, L.G. (ed.) The biology of Crustacea 5, embryology, morphology and genetics, Volume 2. New York: Academic Press, pp. 111–196.Google Scholar
Hines, A.H. (1976) Comparative reproductive ecology of three species of intertidal barnacles. PhD thesis. University of California at Berkeley, USA.Google Scholar
Limbaugh, C., Pederson, H. and Chace, F.A. Jr (1961) Shrimps that clean fishes. Bulletin of Marine Science 11, 237–57.Google Scholar
Rhyne, A.L. and Lin, J. (2006) A western Atlantic peppermint shrimp complex: redescription of Lysmata wurdemanni, description of four new species, and remarks on Lysmata rathbunae (Crustacea: Decapoda: Hippolytidae). Bulletin of Marine Science 79, 165–204.Google Scholar
Rhyne, A., Rotjan, R., Bruckner, A. and Tlusty, M. (2009) Crawling to collapse: ecologically unsound ornamental invertebrate fisheries PLoS One 4(12), e8413. doi: 10.1371/journal.pone.0008413.CrossRefGoogle ScholarPubMed
Tlusty, M. (2002) The benefits and risks of aquacultural production for the aquarium trade. Aquaculture 205, 203–219.CrossRefGoogle Scholar
Turner, R.L. and Lawrence, J.M. (1979) Volume and composition of echinoderm eggs: implications for the use of egg size in life history models. In Stancik, S.E. (ed.) Reproductive ecology of marine invertebrates. Columbia, SC: University of South Carolina Press, pp. 25–40.Google Scholar
Wilson, K. and Hardy, I.C.W. (2002) Statistical analysis of sex ratios: an introduction. In Hardy, I.C.W. (ed.) Sex ratios: concepts and research methods. Cambridge: Cambridge University Press, pp. 48–92.CrossRefGoogle Scholar
Wong, J.W.Y. and Michiels, N.K. (2012) Control of social monogamy through aggression in a hermaphroditic shrimp. Frontiers in Zoology 8, 30.CrossRefGoogle Scholar
Wood, E.M. (2001) Collection of coral reef fish for aquaria: global trade, conservation issues and management strategies. Ross-on-Wye: Marine Conservation Society.Google Scholar
Zar, J.H. (1999) Biostatistical analysis. 4th edition.Englewood Cliffs, NJ: Prentice-Hall.Google Scholar