Effect of natural sedimentation on the structure of tropical rocky sponge assemblagesFootnote

1 Associate Editor: Marco Rodriguez.

Literature cited

• Airoldi, L., 2003. The effects of sedimentation on rocky coast assemblages. Oceanography and Marine Biology, 41: 161–236.
   Google Scholar
• Airoldi, L. & F. Cinelli, 1997. Effects of sedimentation on subtidal macroalgal assemblages: An experimental study from a Mediterranean rocky shore. Journal of Experimental Marine Biology and Ecology, 215: 269–288.
   Google Scholar
• Airoldi, K., M. Fabiano & F. Cinelli, 1996. Sediment deposition and movement over a turf assemblage in a shallow rocky coastal area of the Ligurian Sea. Marine Ecology Progress Series, 133: 241–251.
   Google Scholar
• Alcolado, P. M., 1979. Estructura ecológica de la comunidad de esponjas en un perfil costero de Cuba. Revista Ciencias Biológicas Centro Nacional Investigaciones Científicas (Cuba), 3: 105–127.
   Google Scholar
• Alcolado, P. M., 1989. Estructura ecológica de las comunidades de esponjas del arrecife de Rincón de Guanabo, Cuba. Instituto Oceanología Academia de Ciencias de Cuba, 10: 1–16.
   Google Scholar
• Alcolado, P. M. & A. Herrera, 1987. Efectos de la contaminación sobre las comunidades de esponjas en el litoral de la Habana, Cuba. Reporte Investigación Instituto Oceanología Academia de Ciencias de Cuba, 68: 1–23.
   Google Scholar
• Anderson, F. E. & L. M. Meyer, 1986. The interaction of tidal currents on a disturbed intertidal bottom with a resulting change in particulate matter quantity, texture and food quality. Estuarine, Coastal and Shelf Science, 22: 19–29.
   Google Scholar
• Ávila, E. & J. L. Carballo, 2004. Growth and standing stock biomass of a mutualistic association between the sponge Haliclona caerulea and the red alga Jania adherens. Symbiosis, 36: 225–244.
   Google Scholar
• Battershill, N. & P. R. Bergquist, 1990. The influence of storms on asexual reproduction, recruitment, and survivorship of sponges. Pages 533–545 in K. Rützler (ed.). New Perspectives in Sponge Biology. Smithsonian Institution Press, Washington, DC.
   Google Scholar
• Bavestrello, G., R. Cattaneo-Vietti, R. Canovaro & M. Fabiano, 1991. Detritus rolling down a vertical cliff of the Ligurian Sea (Italy): The ecological role in hard bottom communities. Marine Ecology, 12: 281–292.
   Google Scholar
• Bell, J. J., 2004. Evidence for morphology-induced sediment settlement prevention on the tubular sponge Haliclona urceolus. Marine Biology, 146: 29–38.
   Google Scholar
• Bell, J. J. & D. K. A. Barnes, 2000a. The influences of bathymetry and flow regime upon the morphology of sublittoral sponge communities. Journal of Experimental Marine Biology and Ecology, 80: 707–718.
   Google Scholar
• Bell, J. J. & D. K. A. Barnes, 2000b. The distribution and prevalence of sponges in relation to environmental gradients within a temperate sea lough: Vertical cliff surfaces. Diversity and Distribution, 6: 283–303.
   Google Scholar
• Bell, J. J. & D. K. A. Barnes, 2000c. A sponge diversity centre within a marine “island”. Hydrobiologia, 440: 55–64.
   Google Scholar
• Bell, J. J. & D. K. A. Barnes, 2003. The importance of competitor identity, morphology and ranking methodology to outcomes in interference competition between sponges. Marine Biology, 143: 415–426.
   Google Scholar
• Bell, J. J., D. K. A. Barnes & J. R. Turner, 2002. The importance of micro and macro morphological variation in the adaptation of a sublittoral demosponge to current extremes. Marine Biology, 140: 75–81.
   Google Scholar
• Boury-Esnault, N. & K. Rützler, 1997. Thesaurus of Sponge Morphology. Smithsonian Contributions to Zoology, 596: 1–55.
   Google Scholar
• Burton, M., 1949. Observations on littoral sponges, including the supposed swarming of larvae, movement and coalescence in mature individuals, longevity and death. Proceedings of the Zoological Society of London, 118: 893–915.
   Google Scholar
• Carballo, J. L. & E. Ávila, 2004. Population dynamics of a mutualistic interaction between the sponge Haliclona caerulea, and the red alga Jania adherens. Marine Ecology Progress Series 279: 93–104.
   Google Scholar
• Carballo, J. L. & S. Naranjo, 2002. Environmental health assessment of a large marine industrial complex based on a community of benthic filter-feeders. Marine Pollution Bulletin, 44: 605–610.
   Google Scholar
• Carballo, J. L., S. A. Naranjo & J. C. García-Gómez, 1996. The use of marine sponges as stress indicators in marine ecosystems at Algeciras Bay (southern Iberian Peninsula). Marine Ecology Progress Series, 135: 109–122.
   Google Scholar
• Carballo, J. L., C. Olabarria & T. Garza Osuna, 2002. Analysis of four macroalgal assemblages along the Pacific Mexican coast during and after the 1997-1998 El Niño. Ecosystems, 5: 749–760.
   Google Scholar
• Carballo, J. L., J. E. Sánchez-Moyano & J. C. García-Gómez, 1994. Taxonomical and ecological remarks on boring sponges (Clionidae) from the Straits of Gibraltar (southern Spain): Tentative bioindicators? Zoological Journal of the Linnean Society, 112: 407–424.
   Google Scholar
• Carballo, J. L., P. Gómez, J. A. Cruz-Barraza & D. M. Flores-Sánchez, 2003. Sponges of the Family Chondrillidae (Porifera: Demospongiae) from the Pacific Coast of Mexico, with the description of three new species. Proceedings of the Biological Society of Washington, 116: 515–527.
   Google Scholar
• Clarke, K. R., 1990. Comparisons of dominance curves. Journal of Experimental Marine Biology and Ecology, 138: 143–157.
   Google Scholar
• Clarke, K. R. & R. M. Warwick, 1994. Change in Marine Communities: An Approach to Statistical Analysis and Interpretation. Natural Environment Research Council, Swindon.
   Google Scholar
• CNA (Comisión Nacional del Agua), 2004. Datos estadísticos climáticos del observatorio meteorológico de Mazatlán, Sinaloa, México. Servicio Meteorológico Nacional, México.
   Google Scholar
• Díaz, C. M., B. Alvarez & R. A. Laughlin, 1990. The sponge fauna on a fringing coral reef in Venezuela, II: Community structure. Pages 367–375 in K. Rützler (ed.). New Perspectives in Sponge Biology. Smithsonian Institution Press, Washington, DC.
   Google Scholar
• Elvin, D. W., 1976. Seasonal growth and reproduction of an intertidal sponge, Haliclona permollis (Bowerbank). Biological Bulletin of the Marine Biology Laboratory, Woods Hole, 151: 108–125.
   Google Scholar
• Engledow, H. R. & J. J. Bolton, 1994. Seaweed α-diversity within the lower eulittoral zone in Namibia: The effects of wave action, sand inundation, mussels and limpets. Botanica Marina, 37: 267–276.
   Google Scholar
• Foster, M. S., 1975. Algal succession in a Macrocystis pyrifera forest. Marine Biology, 32: 313–329.
   Google Scholar
• García, E. & C. M. Duarte, 2001. Sediment retention by a Mediterranean Posidonia oceanica meadow: The balance between deposition and resuspension. Estuarine Coastal and Shelf Science, 52: 505–514.
   Google Scholar
• Garrabou, J. & M. Zabala, 2001. Growth dynamics in four Mediterranean demosponges. Estuarine Coastal and Shelf Science, 52: 293–303.
   Google Scholar
• Gibbs, M. M., 2001. Sedimentation, suspension, and resuspension in Tasman Bay and Beatrix Bay, New Zealand, two contrasting coastal environments which thermally stratify in summer. New Zealand Journal of Marine and Freshwater Research, 35: 951–970.
   Google Scholar
• Hooper, J. N. A. & R. W. M. van Soest (eds.), 2002. Systema Porifera: A Guide to the Classification of Sponges. Volume 1. Kluwer Academic / Plenum Publishers, New York, New York.
   Google Scholar
• Inman, D. L., 1952. Measures of describing the size distribution of sediments. Journal of Sedimentology and Petrology, 22: 125–145.
   Google Scholar
• Kaehler, S. & G. A. Williams, 1996. Distribution of algae on tropical rocky shores: Spatial and temporal patterns of non-coralline encrusting algae in Hong Kong. Marine Biology, 125: 177–187.
   Google Scholar
• Kaehler, S. & G. A. Williams, 1998. Early development of algal assemblages under different regimes of physical and biotic factors on a seasonal tropical rocky shore. Marine Ecology Progress Series, 172: 61–71.
   Google Scholar
• Kendrick, G. A., 1981. Recruitment of coralline crusts and filamentous turf algae in the Galapagos archipelago: Effect of simulated scour, erosion and accretion. Journal of Experimental Marine Biology and Ecology, 147: 47–63.
   Google Scholar
• Kröncke, I., J. W. Dippner, H. Heyen & B. Zeiss, 1998. Long-term changes in macrofaunal communities off Norderney (East Frisia, Germany) in relation to climate variability. Marine Ecology Progress Series, 167: 25–36.
   Google Scholar
• Lieberman, M., D. M. John & D. Lieberman, 1979. Ecology of subtidal algae on seasonally devastated cobble substrate off Ghana. Ecology, 60: 1151–1161.
   Google Scholar
• Littler, M. M., D. R. Martz & D. S. Littler, 1983. Effects of recurrent sand deposition on rocky intertidal organisms: Importance of substrate heterogeneity in a fluctuating environment. Marine Ecology Progress Series, 11: 129–139.
   Google Scholar
• Lund-Hansen, L. C., 1991. Sedimentation and sediment accumulation rates in a low-energy embayment. Journal of Coastal Research, 7: 969–980.
   Google Scholar
• Maughan, B. C., 2001. The effects of sedimentation and light on recruitment and development of a temperate, subtidal, epifaunal community. Journal of Experimental Marine Biology and Ecology, 256: 59–71.
   Google Scholar
• McClanahan, T. R., 1988. Seasonality in East Africa’s coastal waters. Marine Ecology Progress Series, 44: 191–199.
   Google Scholar
• McClanahan, T. R., 1990. Kenyan coral reef-associated gastropod assemblages: Distribution and diversity patterns. Coral Reefs, 9: 63–74.
   Google Scholar
• McClanahan, T. R. & J. C. Mutere, 1994. Coral and sea urchin assemblage structure and interrelationships in Kenya reef lagoons. Hydrobiologia, 286: 109–124.
   Google Scholar
• Meroz, E. & M. Ilan, 1995. Life history characteristics of a coral reef sponge. Marine Biology, 124: 443–451.
   Google Scholar
• Monreal, M. A. & D. A. Salas de León, 1998. Dinámica y estructura termohalina. Pages 13–26 in M. Tapia García (ed.). El Golfo de Tehuantepec: el ecosistema y sus recursos. Universidad Autónoma Metropolitana-Iztapalapa, México.
   Google Scholar
• Moore, P. G., 1977. Inorganic particulate suspensions in the sea and their effects on marine animals. Oceanography and Marine Biology Annual Review, 15: 225–363.
   Google Scholar
• Muricy, G., 1991. Structure des peuplements de spongiaires autour de l’égout de Cortiou (Marseille, France). Vie Milieu, 41: 205–221.
   Google Scholar
• Naranjo, S., J. L. Carballo & J. C. García-Gómez, 1996. The effects of environmental stress on ascidian populations in Algeciras Bay (southern Spain). Possible Marine Bioindicators. Marine Ecology Progress Series, 144: 119–131.
   Google Scholar
• Newell, R. C., L. J. Seiderer & D. R. Hitchcock, 1998. The impact of dredging works in coastal waters: A review of the sensitivity to disturbance and subsequent recovery of biological resources on the sea bed. Oceanography and Marine Biology: An Annual Review, 36: 127–178.
   Google Scholar
• Newell, R. C., L. J. Seiderer & J. E. Robinson, 2001. Animal sediment relationships in coastal deposits of the eastern English Channel. Journal of the Marine Biological Association of the United Kingdom, 81: 1–9.
   Google Scholar
• Ormond, R. F. G. & S. A. Banaimoon, 1994. Ecology of intertidal macroalgal assemblages on the Hadramount coast of Southern Yemen, an area of seasonal upwelling. Marine Ecology Progress Series, 105: 105–120.
   Google Scholar
• Palumbi, S. R., 1984. Tactics of acclimation: Morphological changes of sponges in an unpredictable environment. Science, 225: 1478–1480.
   Google Scholar
• Pansini, M. & R. Pronzato, 1990. Observations on the dynamics of a Mediterranean sponge community. Pages 404–415 in K. Rützler (ed.). New Perspectives in Sponge Biology, Smithsonian Institution Press, Washington, DC.
   Google Scholar
• Pearson, T. H. & R. Rosenberg, 1978. Macrobenthic succession relation to organic enrichment and pollution of the marine environment. Oceanography and Marine Biology: An Annual Review, 16: 239–311.
   Google Scholar
• Peraza, V. R., 1985. Transporte Litoral de Arenas en Playas de la Costa Sur del Estado de Sinaloa. M.Sc. thesis, Universidad Autónoma de México, México.
   Google Scholar
• Pickett, S. T. A., J. Kolasa, J. J. Armesto & S. L. Collins, 1989. The ecological concept of disturbance and its expression at various hierarchical levels. Oikos, 54: 129–136.
   Google Scholar
• Pronzato, R. & R. Manconi, 1995. Long-term dynamics of a freshwater sponge population. Freshwater Research, 33: 485–495.
   Google Scholar
• Reiswig, H. M., 1971. Particle feeding in natural populations of three marine demosponges. Biological Bulletin of the Marine Biology Laboratory, Woods Hole, 141: 568–591.
   Google Scholar
• Roth, S. & J. Wilson, 1998. Functional analysis by trophic guilds of macrobenthic community structure in Dublin Bay, Ireland. Journal of Experimental Marine Biology and Ecology, 222: 195–217.
   Google Scholar
• Rützler, K., 1978. Sponges in coral reefs. Pages 299–314 in D. R. Stoddart & R. E. Johannes (eds.). Coral Reefs: Research Methods. Monographs on Oceanographic Methodology 5. UNESCO, Paris.
   Google Scholar
• Saiz Salinas, J. I. & I. Isasi Urdangarin, 1994. Response of sublittoral hard substrate invertebrates to estuarine sedimentation in the outer harbour of Bilbao (N. Spain). Marine Ecology, 15: 105–131.
   Google Scholar
• Saiz-Salinas, J. I. & J. Urkiaga-Alberdi, 1999. Faunal responses to turbidity in a man-modified bay (Bilbao, Spain). Marine Environmental Research, 47: 331–347.
   Google Scholar
• Santos, R., 1993. A multivariate study of biotic and abiotic relationships in a subtidal algal stand. Marine Ecology Progress Series, 94: 181–190.
   Google Scholar
• Sarà, M., 1996. Studio quatitativo della distribuzione dei Poriferi in ambienti superficiali della Riviera Ligure di Levante. Archives of Oceanography and Limnology, 14: 365–386.
   Google Scholar
• Sousa, W. P., 1979. Disturbance in marine intertidal boulder fields: The nonequilibrium maintenance of species diversity. Ecology, 60: 1225–1239.
   Google Scholar
• Steller, D. L., R. Riosmena-Rodríguez, M. S. Foster & C. A. Roberts, 2003. Rhodolith bed diversity in the Gulf of California: The importance of rhodolith structure and consequences of disturbance. Aquatic Conservation: Marine and Freshwater Ecosystems, 13: 5–20.
   Google Scholar
• Stone, A. R., 1970. Growth and reproduction of Hymeniacidon perleve (Montagu) in Langstone Harbour, Hampshire. Journal of Zoology, 161: 443–459.
   Google Scholar
• Storlazzi, C. D. & M. E. Field, 2000. Sediment distribution and transport along a rocky, embayed coast: Monterey Peninsula and Carmel Bay, California. Marine Geology, 170: 289–316.
   Google Scholar
• Suple, C., 1999. El Niño/La Niña. National Geographic 4: 74–95.
   Google Scholar
• Taylor, P. R. & M. M. Littler, 1982. The roles of compensatory mortality, physical disturbance, and substrate retention in the development and organization of a sand-influenced, rockyintertidal community. Ecology, 63: 135–146.
   Google Scholar
• Vacelet, J., 1978. La place des spongiaires dans les écosystèmes trophiques marins. Pages 259–270 in C. Lévi & N. Boury-Esnault (eds.). Biologie des Spongiaires. Colloques Internationaux du Centre National de la Recherche Scientifique Number 291, Paris.
   Google Scholar
• Valderrama, D. & S. Zea, 2003. Esquemas de distribución de esponjas arrecifales (Porifera) del noroccidente del golfo de Urabá, Caribe Sur, Colombia. Boletín Investigación Marina, 32: 37–56.
   Google Scholar
• Vogel, S., 1981. Life in moving fluids. Princeton University Press, Princeton, New Jersey.
   Google Scholar
• Vogt, H. & W. Schramm, 1991. Conspicuous decline of Fucus in Kiel Bay (Western Baltic): What are the causes? Marine Ecology Progress Series, 69: 189–194.
   Google Scholar
• Warwick, R. M., 1986. A new method for detecting pollution effects on marine macrobenthic communities. Marine Biology, 92: 557–562.
   Google Scholar
• Warwick, R. M., 1993. Environmental impact studies on marine communities: Pragmatical considerations. Australian Journal of Ecology, 18: 63–80.
   Google Scholar
• Warwick, R. M., T. H. Pearson & Ruswahyuni, 1987. Detection of pollution effects on marine macrobenthos: Further evaluation of the species abundance/biomass method. Marine Biology, 95: 193–200.
   Google Scholar
• Wesseling, I., A. J. Uychiaoco, P. M. Aliño, T. Aurin & J. E. Vermaat, 1999. Damage and recovery of four Philippine corals from short-term sediment burial. Marine Ecology Progress Series, 176: 11–15.
   Google Scholar
• Wiedenmayer, F., 1977. Shallow-Water Sponges of the Western Bahamas. Birkhäuser Verlag, Basel und Stuttgart.
   Google Scholar
• Wilkinson, C. R. & A. C. Cheshire, 1989. Patterns in the distribution of sponge populations across the central Great Barrier Reef. Coral Reefs, 8: 127–134.
   Google Scholar
• Zea, S., 1994. Patterns of coral and sponge abundance in stressed coral reefs at Santa Marta, Colombia Caribbean. Pages 257–264 in R. W. M. van Soest, T. M. G van Kempen & J. C. Braekman (eds.). Sponges in Time and Space. Balkema, Rotterdam.
   Google Scholar
• Zea, S., 2001. Patterns of sponge (Porifera, Demospongiae) distribution in remote, oceanic reef complexes of the southwestern Caribbean. Revista Colombiana de Ciencias, 25: 579–592.
   Google Scholar