Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-27T13:25:10.163Z Has data issue: false hasContentIssue false

Sclerochronology – a highly versatile tool for mariculture and reconstruction of life history traits of the queen conch, Strombus gigas (Gastropoda)

Published online by Cambridge University Press:  23 October 2009

Pascal Radermacher
Affiliation:
Institute of Geosciences, Earth System Science Research Center (Geocycles) and Increments, University of Mainz, Johann-Joachim-Becherweg 21, 55128 Mainz, Germany
Bernd R. Schöne
Affiliation:
Institute of Geosciences, Earth System Science Research Center (Geocycles) and Increments, University of Mainz, Johann-Joachim-Becherweg 21, 55128 Mainz, Germany
Eberhard Gischler
Affiliation:
Institute of Geosciences, Goethe-University, Altenhöferallee 1, 60438 Frankfurt am Main, Germany
Wolfgang Oschmann
Affiliation:
Institute of Geosciences, Goethe-University, Altenhöferallee 1, 60438 Frankfurt am Main, Germany
Julien Thébault
Affiliation:
Institut Universitaire Européen de la Mer, Université de Bretagne Occidentale Laboratoire des Sciences de l'Environnement marin, UMR 6539 (UBO/IRD/CNRS), Technopôle Brest-Iroise, Place Nicolas Copernic, 29280 Plouzané, France
Jens Fiebig
Affiliation:
Institute of Geosciences, Goethe-University, Altenhöferallee 1, 60438 Frankfurt am Main, Germany
Get access

Abstract

The queen conch, Strombus gigas, is an important fisheries resource in the Western Tropical Atlantic. In order to maintain harvesting success, improve fisheries management and contribute to mariculture pursuits, a detailed understanding of the life history traits of this species is required. Traditionally, this has been achieved by tedious and time-consuming long-term field observations. This study presents a highly versatile and rapid technique to estimate the timing and rate of shell growth based on sclerochronology. The Belizean S. gigas specimens (N = 2) from the offshore atoll, Glovers Reef, reached their final shell size (maximum shell height: 22.7 and 23.5 cm, respectively; completed formation of the flared lip) after only two years. However, seasonal growth rates varied considerably. Shells grew up to 6 mm d−1 during spring (April-June) and fall (September-November) but only 1 to 2 mm d−1d uring July and August. Furthermore, shell growth ceased between December and March. Fastest shell growth occurred nearly contemporaneously with times of maximum precipitation which probably resulted in increased food availability. Slowest shell growth however, occurred during times of reduced rainfall and reduced riverine runoff, i.e. during times of reduced food supply. Sea-water temperature apparently did not exert a major control on shell growth. Notably, the slow winter growth was marked by a distinct purple-colored growth line in the cross-sectioned flared lip. Formation of a second major growth line (brown) fell together with the main reproduction period (late October/early November). Shell microgrowth patterns potentially represent daily or semidiurnal periods but cannot be used to assign exact calendar dates to each shell portion, because they were not visible across the entire cross-section of the whorl. Also, the protruding spines developed on the outer shell surface do not function as time gauges. The time represented by the shell portion between consecutive spines varies greatly from 1 to 72 days. Sclerochronology can potentially facilitate maricultural strategies and aid in site pre-testing and selection to grow S. gigas.

Type
Research Article
Copyright
© EDP Sciences, IFREMER, IRD, 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Alcolado, P.M., 1976, Crecimiento, variaciones morfologicas de la concha y algunas datos biologicos del cobo Strombus gigas L. (Mollusca, Mesogastropoda). Acad. Cienc. Cuba Ser. Oceanol. 34, 136.
Appeldoorn, R.S., 1985, Growth, mortality and dispersion of juvenile, laboratory-reared conchs, Strombus gigas and S. costatus, released at an offshore site. Bull. Mar. Sci. 37, 785793.
Appeldoorn, R.S., 1988, Age determination, growth, mortality and age of first reproduction in adult queen conch, Strombus gigas L., off Puerto Rico. Fish. Res. 6, 363378. CrossRef
Berg, C.J., 1976, Growth of the queen conch Strombus gigas, with a discussion of the practicality of its mariculture. Mar. Biol. 34, 191199. CrossRef
Böhm, F., Joachimski, M.M., Dullo, W.C., Eisenhauer, A., Lehnert, H., Reitner, J., Worheide, G., 2000, Oxygen isotope fractionation in marine aragonite of coralline sponges. Geochim. Cosmochim. Acta. 64, 16951703. CrossRef
Buddemeier, R.W., Maragos, J.E., 1974, Radiographic studies of reef coral exoskeletons: rates and patterns of coral growth. J. Exp. Mar. Biol. Ecol. 14, 179200. CrossRef
Burke, R.B., 1982, Reconnaissance study of the geomorphology and benthic communities of the outer barrier reef platform, Belize. Smiths. Contr. Mar. Sci. 12, 509526.
Campton, D.E., Berg, C.J., Robison, L.M., Glazer, R.A., 1992, Genetic patchiness among populations of queen conch Strombus gigas in the Florida Keys and Bimini. Fish. Bull. 90, 250259.
Coulston, M.L., Berey, R.W., Dempsey, A.C., Odum, P., 1989, Assessment of the queen conch (Strombus gigas) population and predation studies of hatchery reared juveniles in Salt River Canyon, St. Croix, USVI. Proc. Gulf. Caribb. Fish. Inst. 38, 294305.
Curtis, S., Gamble, D.W., 2008, Regional variations of the Caribbean mid-summer drought. Theor. Appl. Climatol. 94, 2534. CrossRef
Dettman, D.L., Reische, A.K., Lohmann, K.C., 1999, Controls on the stable isotope composition of seasonal growth bands in aragonitic freshwater bivalves (Unionidae). Geochim. Cosmochim. Acta 63, 10491057. CrossRef
Epstein, S., Lowenstam, H., 1953, Temperature-shell-growth relations of recent and interglacial Pleistocene shoal-water biota from Bermuda. J. Geol. 61, 424437. CrossRef
Epstein, S., Buchsbaum, R., Lowenstam, H., Urey, H.C., 1953, Revised carbonate water-temperature scale. Geol. Soc. Am. Bull. 64, 13151326. CrossRef
Ezer, T., Thattai, D.V., Kjerfve, B., Heyman, W.D., 2005, On the variability of the flow along the Meso-American Barrier Reef system: a numerical model study of the influence of the Caribbean current and eddies. Ocean. Dyn. 55, 458475. CrossRef
Gischler, E., 2003, Holocene lagoonal development in the isolated carbonate platforms off Belize. Sediment. Geol. 159, 113132. CrossRef
Gischler E., Lomando A.J., 2000, Isolated carbonate platforms of Belize, Central America: sedimentary facies, late Quaternary history and controlling factors. In: Insalaco E., Skelton P.W., Palmer T.J. (Eds.) Carbonate platform systems: components and interactions. Geol. Soc. Special. Pub. 178. The Geological Society, London, pp. 135–146.
Gischler, E., Hauser, I., Heinrich, K., Scheitel, U., 2003, Characterization of depositional environments in isolated carbonate platforms based on benthic foraminifera, Belize, Central America. Palaios 18, 236255. 2.0.CO;2>CrossRef
Hauser, I., Oschmann, W., Gischler, E., 2007, Modern bivalve shell assemblages on three atolls offshore Belize (Central America, Caribbean Sea). Facies 53, 451478. CrossRef
Jones, D.S., 1980, Annual cycle of shell growth increment formation in two continental shelf bivalves and its paleoecologic significance. Paleobiology 6, 331340. CrossRef
Keith, M.L., Anderson, G.M., Eichler, R., 1964, Carbon and oxygen isotopic composition of mollusk shells from marine and fresh-water environments. Geochim. Cosmochim. Acta. 28, 17571786. CrossRef
Kobashi, T., Grossman, E.L., 2003, The oxygen isotopic record of seasonality in Conus shells and its application to understanding late middle Eocene (38 Ma) climate. Paleontol. Res. 7, 343355. CrossRef
Lorrain, A., Paulet, Y.M., Chauvaud, L., Savoye, N., Donval, A., Saout, C., 2002, Differential delta C-13 delta N-15 signatures among scallop tissues: implications for ecology and physiology. J. Exp. Mar. Biol. Ecol. 275, 4761. CrossRef
Magaña, V., Amador, J.A., Medina, S., 1999, The mid summer drought over Mexico and Central America. J. Clim. 12, 15771588. 2.0.CO;2>CrossRef
Magaña V., Caetano E., 2005, Temporal evolution of summer convective activity over the Americas warm pools. Geophys. Res. Lett. 32 [DOI:10.1029/2004GL021033] CrossRef
Martín-Mora, E., James, F.C., Stoner, A.W., 1995, Developmental plasticity in the shell of the queen conch Strombus gigas. Ecology 76, 981994. CrossRef
Randall, J.E., 1964, Contributions to the biology of the queen conch Strombus gigas. Bull. Mar. Sci. Gulf. Caribb. 14, 246295.
Robertson, R., 1961, The feeding of Strombus gigas and related herbivorous marine gastropods: With a review and field observations. Notulae Naturae 343, 19.
Santarelli, L., Gros, P., 1985, Détermination de l'âge et de la croissance de Buccinum undatum L. (Gastropoda: Prosobranchia) à l'aide des isotopes stable de la coquille et de l'ornementation operculaire. Oceanol. Acta 8, 221229.
Sato, S., 1995, Spawning periodicity and shell microgrowth patterns of the venerid bivalve Phacosoma japonicum (Reeve, 1850). Veliger 38, 6172.
Schmidt G.A., Bigg G.R., Rohling E.J., 1999, Global seawater oxygen-18 database. http://data.giss.nasa.gov/o18data/
Schöne, B.R., Dunca, E., Fiebig, J., Pfeiffer, M., 2005, Mutvei's solution: an ideal agent for resolving microgrowth structures of biogenic carbonates. Palaeogeogr. Palaeoclimatol. Palaeoecol. 228, 149-166. CrossRef
Schöne, B.R., Rodland, D.L., Wehrmann, A., Heidel, B., Oschmann, W., Zhang, Z., Fiebig, J., Beck, L., 2007, Combined sclerochronologic and oxygen isotope analysis of gastropod shells (Gibbula cineraria, North Sea): life-history traits and utility as a high-resolution environmental archive for kelp forests. Mar. Biol. 150, 1237-1252. CrossRef
Stoddart, D.R., 1962, Three Caribbean atolls: Turneffe Islands, Lighthouse Reef, and Glover's Reef, British Honduras. Atoll Res. Bull. 87, 1-147. CrossRef
Stoner, A.W., 1994, Significance of habitat and stock pre-testing for enhancement of natural fisheries: experimental analyses with Queen Conch Strombus gigas. J. World Aquac. Soc. 25, 155-165. CrossRef
Stoner, A.W., Waite, J.M., 1991, Trophic biology of Strombus gigas in nursery habitats: diet and food sources in seagrass meadows. J. Moll. Stud. 57, 451-460. CrossRef
Stoner, A.W., Pitts, P.A., Armstrong, R.A., 1996, Interaction of physical and biological factors in the large-scale distribution of juvenile queen conch in seagrass meadows. Bull. Mar. Sci. 58, 217-233.
Tang L., Sheng J., Hatcher B.G., Sale P.F., 2006, Numerical study of circulation. Dispersion, and hydrodynamic connectivity of surface waters on the Belize shelf. J. Geophys. Res. [DOI 10.1029/2005JC002930]
Theile, S., 2005, Status of the queen conch Strombus gigas stocks, management and trade in the Caribbean: a CITES review. Proc. Gulf. Caribb. Fish. Inst. 56, 676-698.
Thompson, I., Jones, D.S., Ropes, J.W., 1980, Advanced age for sexual maturity in the ocean quahog Arctica islandica (Mollusca: Bivalvia). Mar. Biol. 57, 35-39. CrossRef
Wefer, G., Killingley, J.S., 1980, Growth histories of strombid snails from Bermuda recorded in their O-18 and C-13 profiles. Mar. Biol. 60, 129-135. CrossRef
Wefer, G., Berger, W.H., 1991, Isotope paleontology: growth and composition of extant species. Mar. Geol. 100, 207-248. CrossRef
Weil, E., Laughlin, R., 1984, Biology, population dynamics, and reproduction of the queen conch, Strombus gigas Linne, in the Archipelago de Los Roques National Park. J. Shellfish Res. 4, 4562.