Abstract
Skeletal extension (3.67 ± 0.65 mm year−1), density (1.49 ± 0.16 g cm−3), and calcification rate (0.55 ± 0.12 g cm−2 year−1) were determined using annual growth bands of Porites astreoides skeletons collected in three different reef systems in the Western Atlantic. The corals showed a low-density annual growth band at their apex, and seasonal timing of low and high-density band formation in P. astreoides appears to be similar at the three study sites in the Western Atlantic. The range of values presented here, for the three growth variables, spans the known range of skeletal-growth variability in P. astreoides for the Western Atlantic. The relationships between the growth parameters were similar to those previously described by other authors for massive Porites species from the Indo-Pacific, suggesting that P. astreoides has the same growth strategy, primarily investing calcification resources in extension rate. It is noteworthy that the P. astreoides population growing off the northwest coast of Cuba had similar growth characteristics as populations from the Caribbean region which were different from populations in the Gulf of Mexico, which seem to be isolated and adapted for growth at higher average sea-surface temperatures.




References
Barnes DJ, Lough JM (1992) Systematic variations in the depth of skeleton occupied by coral tissue in massive colonies of Porites from the Great Barrier Reef. J Exp Mar Biol Ecol 159:113–128
Barnes DJ, Lough JM (1993) On the nature and causes of density banding in massive coral skeletons. J Exp Mar Biol Ecol 167:91–108
Barnes DJ, Lough JM (1996) Coral skeletons: storage and recovery of environmental information. Global Change Biol 2:569–582
Barnes DJ, Lough JM (1999) Porites growth characteristics in a changed environment: Misima Island, Papua New Guinea. Coral Reefs 18:213–218
Brown BE, Lee Tissier M, Howard LS, Charuchinda M, Jackson JA (1986) Asynchronous deposition of dense skeletal bands in Porites lutea. Mar Biol 93:83–89
Buddemeier RW (1974) Environmental controls over annual and lunar monthly cycles in hermatypic coral calcification. Proc 2nd Int Coral Reef Symp 2:259–267
Cairns SD (1999) Species richness of recent Scleractinia. Atoll Res Bull 59:1–46
Carricart-Ganivet JP (2004) Sea surface temperature and the growth of the West Atlantic reef-building coral Montastraea annularis. J Exp Mar Biol Ecol 302:249–260
Carricart-Ganivet JP (2007) Annual density banding in massive coral skeletons: result of growth strategies to inhabit reefs with high microborers’ activity? Mar Biol 153:1–5
Carricart-Ganivet JP, Barnes DJ (2007) Densitometry from digitized images of X-radiographs: Methodology for measurement of coral skeletal density. J Exp Mar Biol Ecol 344:67–72
Carricart-Ganivet JP, González-Diaz P (2009) Growth characteristics of skeletons of Montastraea annularis (Cnidaria: Scleractinia) from the northwest coast of Cuba. Cien Mar 35:237–243
Carricart-Ganivet JP, Merino M (2001) Growth responses of the reef-building coral Montastraea annularis along a gradient of continental influence in the southern Gulf of Mexico. Bull Mar Sci 68:133–146
Carricart-Ganivet JP, Lough JM, Barnes DJ (2007) Growth and luminescence characteristics in skeletons of massive Porites from a depth gradient in the central Great Barrier Reef. J Exp Mar Biol Ecol 351:27–36
Cortés J, Risk MJ (1985) A reef under siltation stress: Cahuita, Costa Rica. Bull Mar Sci 36:339–356
Cruz-Piñón G, Carricart-Ganivet JP, Espinoza-Avalos J (2003) Monthly skeletal extension rates of the hermatypic corals Montastraea annularis and Montastraea faveolata: biological and environmental controls. Mar Biol 143:491–500
Dávalos-Dehullu E, Hernández-Arana H, Carricart-Ganivet JP (2008) On the causes of density banding in skeletons of corals of the genus Montastraea. J Exp Mar Biol Ecol 365:142–147
Dodge RE, Brass GW (1984) Skeletal extension, density and calcification of the reef coral Montastrea annularis: St. Croix US Virgin Islands. Bull Mar Sci 34:288–307
Dodge RE, Vaisnys JR (1975) Hermatypic coral growth banding as environmental recorder. Nature 258:706–708
Dodge RE, Aller RC, Thomson J (1974) Coral growth related to resuspension of bottom sediments. Nature 247:574–577
Edinger EN, Limmon GV, Jompa J, Widjatmoko W, Heikoop JM, Risk MJ (2000) Normal coral growth rates on dying Reefs: are coral growth rates good indicators of reef health? Mar Pollut Bull 40:404–425
Fang LS, Chen YWJ, Chen CS (1989) Why does the tip of stony coral grow so fast without zooxanthellae? Mar Biol 103:359–363
Flor TH, Moore WS (1977) Radium/calcium and uranium/calcium determinations for western Atlantic reef corals. Proc 3rd Int Coral Reef Symp 2:555–561
González-Sansón G, Aguilar C, Hernández I, Cabrera Y, Curry A (2009) The influence of habitat and fishing on reef fish assemblages in Cuba. Gulf Carrib Res 21:13–21
Goreau TF (1959) The ecology of Jamaican coral reefs I. Species composition and zonation. Ecology 40:67–89
Guzmán HM, Cortés J (1989) Growth rates of eight species of scleractinian corals in the eastern Pacific (Costa Rica). Bull Mar Sci 44:1186–1194
Highsmith RC (1979) Coral growth rates and environmental control of density banding. J Exp Mar Biol Ecol 37:105–125
Highsmith RC, Lueptow RL, Schonberg SC (1983) Growth and bioerosion of three massive corals on the Belize barrier reef. Mar Ecol Progr Ser 13:261–271
Horta-Puga G, Carricart-Ganivet JP (1990) Stylaster roseus (Pallas, 1766): First record of a Stylasterid (Cnidaria: Hydrozoa) in the Gulf of Mexico. Bull Mar Sci 47:575–576
Hudson JH, Shinn EA, Halley RB, Lidz B (1976) Sclerochronology: A tool for interpreting past environments. Geol 4:361–364
Jordán-Dahlgren E (1992) Recolonization patterns of Acropora palmata in a marginal environment. Bull Mar Sci 51:104–117
Jordán-Dahlgren E (2002) Gorgonian distribution patterns in coral reef environments of the Gulf of Mexico: Evidence of sporadic ecological connectivity? Coral Reefs 21:205–215
Knutson DW, Buddemeier RW, Smith SV (1972) Coral chronometers: seasonal growth bands in reef corals. Science 177:270–272
Lough JM, Barnes DJ (1990) Possible relationships between environmental variables and skeletal density in a coral colony from the Central Great Barrier Reef. J Exp Mar Biol Ecol 134:221–241
Lough JM, Barnes DJ (1992) Comparisons of skeletal density variations in Porites from the Central Great Barrier Reef. J Exp Mar Biol Ecol 155:1–25
Lough JM, Barnes DJ (1997) Several centuries of variation in skeletal extension, density and calcification in massive Porites colonies from the Great Barrier Reef: a proxy for seawater temperature and a background of variability against which to identify unnatural change. J Exp Mar Biol Ecol 211:29–67
Lough JM, Barnes DJ (2000) Environmental controls on growth of the massive coral Porites. J Exp Mar Biol Ecol 245:225–243
Mallela J, Perry CT (2007) Calcium carbonate budgets for two coral reefs affected by different terrestrial runoff regimes, Rio Bueno, Jamaica. Coral Reefs 26:129–145
Merino M (1997) Upwelling on the Yucatan Shelf: Hydrographic evidence. J Mar Res 13:101–121
Merino M, Czitrom S, Jordán E, Martin E, Thome P, Moreno O (1990) Hydrology and rain flushing of the Nichupté Lagoon System, Cancún, Mexico. Estuar Coast Shelf Sci 30:223–237
Oficina Nacional de Estadística (2005) Censo de población y viviendas, Cuba 2002. Informe Nacional. República de Cuba, p 400
Potts DC, Done TJ, Isdale PJ, Fisk DA (1985) Dominance of a coral community by the genus Porites (Scleractinia). Mar Ecol Prog Ser 23:79–84
Rayner NA, Parker DE, Horton EB, Folland CK, Alexander LV, Rowell DP, Kent EC, Kaplan A (2003) Global analyses of sea surface temperature, sea ice, and night marine air temperature since the late nineteenth century. J Geophys Res.108, 4407. doi:10.1029/2002JD002670
Scoffin TP, Tudhope AW, Brown BE, Chansang H, Cheeney RF (1992) Patterns and possible environmental controls of skeletogenesis of Porites lutea, South Thailand. Coral Reefs 11:1–11
Taylor RB, Barnes DJ, Lough JM (1993) Simple models of density band formation in massive corals. J Exp Mar Biol Ecol 167:109–125
Tomascik T, Sander F (1985) Effects of eutrophication on reef-building corals I. Growth rate of the reef-building coral Montastrea annularis. Mar Biol 87:143–155
Veron JEN (2000) Corals of the World, vol. 3. Australian Institute of Marine Science & CRR Qld Pty Ltd, Australia
Wórum FP, Carricart-Ganivet JP, Benson L, Golicher D (2007) Simulation and observations of annual density banding in skeletons of Montastraea (Cnidaria : Scleractinia) growing under thermal stress associated with ocean warming. Limnol Oceanogr 52:2317–2323
Zavala-Hidalgo J, Parés-Sierra A, Ochoa J (2002) Seasonal variability of the temperature and heat fluxes in the Gulf of Mexico. Atmósfera 15:81–104
Zavala-Hidalgo J, Morey SL, O’Brien JJ (2003) Seasonal circulation on the western shelf of the Gulf of Mexico using a high-resolution numerical model. J Geophys Res 108(C12):3389. doi:10.1029/2003JC001879
Acknowledgments
The manuscript was notably improved by comments of L. Benson, J. Espinoza-Ávalos, G. Leyte-Morales, and three anonymous reviewers. We thank I. Rodríguez-Mauri and C. Varela (Centro de Investigaciones Marinas, Universidad de La Habana), and A.U. Beltrán-Torres, H. Hernández-Arana and L.M. Hernández-Ballesteros (ECOSUR), and J.L. Tello-Musi (FESI, UNAM) for their assistance with field collections. Special thanks to the staff of the “Parque Sistema Arrecifal Veracruzano”, for the facilities provided during the fieldwork. During the investigation, E.M. Elizalde-Rendón was in the Postgraduates Program of ECOSUR and had a scholarship from CONACYT. D. Gugenheim (Harte Research Institute) sponsored part of the fieldwork. This research was supported by grants from CONACYT (project U48757-F), and CONABIO (project DM005).
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Elizalde-Rendón, E.M., Horta-Puga, G., González-Diaz, P. et al. Growth characteristics of the reef-building coral Porites astreoides under different environmental conditions in the Western Atlantic. Coral Reefs 29, 607–614 (2010). https://doi.org/10.1007/s00338-010-0604-7
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DOI: https://doi.org/10.1007/s00338-010-0604-7