19 research outputs found

    Coral Settlement on Oil/Gas Platforms in the Northern Gulf of Mexico: Preliminary Evidence of Rarity

    Get PDF
    In recent decades, there have been two areas of shallow hard substrate available for zooxanthellate coral colonization in the North Gulf of Mexico: the Flower Garden Banks (FGB) and oil and gas platforms. We assessed coral recruitment on platforms possessing adult corals around the FGB. In this preliminary experiment, we used terra cotta plates mounted on racks, deployed on six platforms at depths of 15–27 m for a duration of ≤1 yr in two consecutive years. Data on coral spat taxonomic identification, distribution, and densities were collected. Platform spat densities on plates averaged \u3c1/450 cm2, a low value when compared with the East-FGB (E-FGB; data from earlier similar experiment), other Caribbean sites, or the Great Barrier Reef. Spat density was not significantly different between platforms, suggesting that distance between the platforms and the E-FGB, a potential larval source, was large enough (\u3e0.6–1.2 km) to permit extensive larval diffusion. Total spat density also did not vary significantly between settlement racks, indicating that settlement at the spatial scale of meters was relatively homogeneous. Only three species of spat were found—Tubastraea coccinea, Madracis decactis, and Montastraea sp.; the taxonomic composition of coral spat varied from those observed earlier on the E-FGB—Agaricia and Porites. The dominant recruits matched the dominant adults on the platforms— an unusual situation. Tubastraea and Madracis spat densities, respectively, did not vary significantly between platforms or between racks. Because of low recruitment levels, these artificial reef communities may be considered fragile in comparison to many natural ones because of the time required for recovery in the event of a mass coral mortality. These low recruitment levels, however, when integrated over ~30 yr, can result in the successful establishment of adult coral communities on the platforms

    New Fission Processes In The Zoanthid Palythoa Caribaeorum: Description And Quantitative Aspects

    No full text
    Populations of the zoanthid Palythoa caribaeorum (Duchassaing and Michelotti, 1861) were monitored in a 2-yr study at several sites on the São Paulo coast, Brazil, to describe, quantify, and compare fission processes occurring in moderately vs. highly stressed environments. The effects of depth and season were also considered. Palythoa caribaeorum was found to reproduce by two new general processes of fission. The first process requires: A) the formation of crevices throughout the colony and the maintenance of basal coenenchyme throughout; B) the production of polyp-clusters which are connected to each other by thin basal coenenchyme, not readily visible; and C) the subsequent severance of the basal coenenchyme between polyp-clusters, creating true ramets. The first process included two variants: edge fission and polyp-cluster release. The second fission process was characterized by directional growth of tissue and a subsequent breaking away and dispersing of the ramets. It also included two variants: tissue outgrowth and polyp-ball production. Of the monitored colonies, 55% (nt = 579) exhibited at least one variant of fission, yielding 1304 ramets over 1 yr. Edge fission was the dominant form of asexual reproduction in this species. We found no evidence to support the hypothesis that higher environmental stress results in increased ramet production among sites, depths, or seasons. Fission occurred year-round and in colonies of all sizes. The minimum size of a colony reproducing by fission was 5 cm2. A significant positive linear relationship was found between colony area and number of ramets produced per colony. Ramet release also occurred year-round, although the frequency of release was significantly lower during the winter, when environmental conditions were harsher. This is the first report of tissue outgrowth, polyp-ball production, and polyp-cluster release for the genus Palythoa, and the first report of polyp-ball production within the Zoanthidea. There appear to be no analogues of polyp-cluster release within the Cnidaria. Fission in P. caribaeorum appears to be a conservative trait over a wide geographical range. It also seems to be endogenously controlled (genetically programmed) responding to colony growth constraints. Exogenous factors, however, may help to define the variant of fission used and the quantity of ramets produced at a given time. The adaptive value of fission for P. caribaeorum lies in its contribution to the number of clone-mates (increasing population size). It represents a critical and important form of asexual reproduction, helping to explain the ecological and evolutionary success of this species in the western Atlantic.761126Acosta, A., (1999) Ecologia Da Reprodução Assexuada de Palythoa caribaeorum (Zoanthidea: Cnidaria), 215p. , Tese de Doutor, Instituto de Biologia, Universidade Estadual de Campinas, S.P. BrazilDisease in zoanthids: Dynamics in space and time (2001) Hydrobiologia, 460, pp. 113-130Asbahr, M., Reproductive effort in Palythoa caribaeorum (2000) Proc. 9th Int. Coral Reef Symp., p. 295. , Bali. AbstractSammarco, P.W., Duarte, L.F., Asexual reproduction in a zoanthid by fragmentation (2001) Bull. Mar. Sci., 68, pp. 363-381Akcakaya, H.R., Burgman, M.A., Ginzburg, L.R., Applied population ecology: Principles and computer exercises using RAMAS Ecolab 1.0 (1997) Applied Biomathematics, 255p. , SetauketAnthony, K.R.N., Prey capture by the sea anemone Metridium senile: Effects of body size, flow regime, and upstream neighbors (1997) Biol. Bull., 192, pp. 73-86Ayre, D.J., Resing, J.M., Sexual and asexual production of planulae in reef corals (1986) Mar. Biol., 90, pp. 187-190Bell, G., (1982) The Masterpiece of Nature: The Evolution and Genetics of Sexuality, 635p. , Croom Helm, London and CanberraBurnett, W.J., Benzie, J.A.H., Beardmore, J.A., Ryland, J.S., High genetic variability and patchiness in a common Great Barrier Reef zoanthid (Palythoa caesia) (1994) Mar. Biol., 121, pp. 153-160Patterns of genetic subdivision in populations of a clonal cnidarian, Zoanthus coppingeri, from the Great Barrier Reef (1995) Mar. Biol., 122, pp. 665-673Bucklin, A., Growth and asexual reproduction of the sea anemone Metridium: Comparative laboratory studies of three species (1987) J. Exp. Mar. Biol. Ecol., 110, pp. 41-52Cairns, S.D., Asexual reproduction in solitary scleractinia (1988) Proc. 6th Int. Coral Reef Symp., 2, pp. 641-645. , TownsvilleCalgren, O., Ceriantharia and Zoantharia. British Museum (Natural History), Great Barrier Reef Expedition 1928-1929 (1937) Scientific Reports, 5 (5), pp. 25-209Cameron, A.M., Endean, R., Do long-lived species structure coral reefs ecosystems (1985) Proc. 5th Int. Coral Reef Congr., 6, pp. 211-215. , TahitiChao, S.M., Tsai, C.C., Reproduction and population dynamics of the fissiparous brittle star Ophiactis savignyi (Echinodermata: Ophiuroidea) (1995) Mar. Biol., 124, pp. 77-83Chia, F.S., Sea anemone reproduction: Patterns and adaptive radiations (1976) Coelenterate Ecology and Behavior, pp. 261-269. , G. O. Mackie, ed. Plenum Press, New YorkCoates, A.G., Jackson, J.B.C., Morphological themes in the evolution of clonal and aclonal marine invertebrates (1985) Population Biology and Evolution of Clonal Organisms, pp. 67-106. , J.B.C. Jackson, L.W. Buss, and R.E. Cook, eds. Yale University Press, New HavenCook, R.E., Asexual reproduction: A further consideration (1978) Amer. Nat., 113, pp. 769-772Clonal plant populations (1983) Am. Sci., 71, pp. 244-253Growth and development in clonal plant populations (1985) Population Biology and Evolution of Clonal Organisms, pp. 259-296. , J.B.C. Jackson, L.W. Buss, and R.E. Cook, eds. Yale University Press, New HavenCooke, W.J., Reproduction, growth, and some tolerances of Zoanthus pacificus and Palythoa vestitus in Kaneohe Bay, Hawaii (1976) Coelenterate Ecology and Behavior, pp. 281-288. , G.O. Mackie, ed. Plenum Press, New YorkCrowell, S., Oates, S., Metamorphosis and reproduction by transverse fission in an Edwardsiid anemone (1980) Developmental and Cellular Biology of Coelenterates, pp. 139-142. , P. Tardent and R. Tarden, eds. Elsevier Press, AmsterdamDahan, M., Benayahu, Y., Clonal propagation by the azooxanthellate octocoral Dendronephthya hemprichi (1997) Coral Reefs, 16, pp. 5-12DeVantier, L.M., Endean, R., Observations of colony fission following ledge-formation in massive reef corals of the genus Porites (1989) Mar. Ecol. Prog. Ser., 58, pp. 191-195Diaz, J.M., Barrios, L.M., Cedales, M.H., Garzon-Ferreira, J., Geister, J., Lopez-Victoria, M., Ospina, G.H., Zea, S., (2000) Áreas Coralinas de Colombia, 176p. , Serie Publicaciones Especiales, No. 5. INVEMAR, Santa MartaDinesen, Z.D., Aspects of the life history of a stolon-bearing species of Efflatounaria (Octocorallia: Xeniidae) (1985) Proc. 5th Int. Coral Reef Congress, 6, pp. 89-94. , TahitiDuerden, J.E., Jamaican Actiniaria, Part I. The Zoantheae (1898) Trans. Roy. Dub. Soc., 6, pp. 329-384. , N.SEmson, R.H., Mladenov, P.V., Studies of the fissiparous holothurian Holothuria parvula (Echinodermata: Holothuroidea) (1987) J. Exp. Mar. Biol. Ecol., 111, pp. 195-211Fadlallah, Y.H., (1981) The Reproductive Biology of Three Species of Corals from Central California, 213p. , Ph.D. Diss., University of California, Santa CruzReproductive ecology of the coral Astrangia lajollaensis: Sexual and asexual patterns in a kelp forest habitat (1982) Oecologia, 55, pp. 379-388Karlson, R.H., Sebens, K.P., A comparative study of sexual reproduction in three species of Panamanian zoanthids (Coelenterata: Anthozoa) (1984) Bull. Mar. Sci., 35, pp. 80-89Gleibs, S., (1994) Role of a Toxic Secondary Metabolite in the Ecology of the Genus Palythoa (Anthozoa) a Zoanthid of the Caribbean, 107p. , Institut für Allgemeine und Spezielle Zoologie, Biologie, Thesis, Justus-Liebig-Universität Gießen, GermanyGonzález, A.M., (1999) Efecto del Tamaño Colonial en la Frecuencia de Fisión de Palythoa caribaeorum (Cnidaria: Zoanthidea) en Santa Marta, Caribe Colombiano, 60p. , Pontificia Universidad Javeriana, Facultad de Ciencias Básicas, Biología, Bogotá, Tesis de Grado de BiólogoAcosta, A., Colony size, fission, and effect of ramets to population growth in the zoanthid Palythoa caribaeorum (2000) 9th Int. Coral Reef Symp., p. 308. , Bali, IndonesiaHaddon, A.C., Shackleton, A.M., Actiniae: I Zoantheae. Reports on the Zoological Collections made in Torres Straits by A.C. Haddon, 1888-1889 (1891) Scient. Trans. R. Soc. Ser. 2, 4, pp. 674-699Harper, J.L., (1977) Population Biology of Plants, 890p. , Academic Press, New YorkHarrison, P.L., Wallace, C.C., Coral reproductive biology (1990) Ecosystems of the World, 25, Coral Reefs, pp. 181-183. , Z. Dubinsky, ed. Elsevier, New YorkHighsmith, R.C., Reproduction by fragmentation in corals (1982) Mar. Ecol. Prog. Ser., 7, pp. 207-226Riggs, A.C., DÁntonio, C.M., Survival of hurricane-generated coral fragments and a disturbance variant of reef calcification growth rates (1980) Oecologia, 46, pp. 322-329Hughes, R.N., (1989) A Functional Biology of Clonal Animals, 331p. , Chapman and Hall, New YorkHughes, T.P., Jackson, J.B.C., Do corals lie about their age? Some demographic consequences of partial mortality, fission and fusion (1980) Science, 209, pp. 713-715Jackson, J.B.C., Population dynamics and life histories of foliaceous corals (1985) Ecol. Monogr., 55, pp. 141-166Hunter, T., The energetics of asexual reproduction: Pedal laceration in the symbiotic sea anemone Aiptasia pulchella (1984) J. Exp. Mar. Ecol., 83, pp. 127-147Jackson, J.B.C., Buss, L.W., Cook, R.E., (1985) Population Biology and Evolution of Clonal Organisms, 465p. , Yale University Press, New HavenJohnson, L.L., Shick, J.M., Effects of fluctuating temperature and immersion on asexual reproduction in the intertidal sea anemone Haliplanella luciae (Verrill) in laboratory culture (1977) J. Exp. Mar. Biol. Ecol., 28, pp. 141-149Karlson, R.H., Disturbance and monopolization of a spatial resource by Zoanthus sociatus (Coelenterata, Anthozoa) (1983) Bull. Mar. Sci., 33, pp. 118-131Disturbance, colonial fragmentation, and size-dependent life history variation in two coral reef cnidarians (1986) Mar. Ecol. Prog. Ser., 28, pp. 245-249Size-dependent growth in two zoanthid species: A contrast in clonal strategies (1988) Ecology, 69, pp. 1219-1232Growth and survivorship of clonal fragments in Zoanthus solanderi Lesueur (1988) J. Exp. Mar. Biol. Ecol., 123, pp. 31-39Fission and the dynamics of genets and ramets in clonal cnidarian populations (1991) Hydrobiologia, 216, pp. 235-240Hughes, T.P., Karlson, S.R., Density-dependent dynamics of soft coral aggregations: The significance of clonal growth and form (1996) Ecology, 77, pp. 1592-1599Kimura, S., Hashimoto, Y., Yamazato, K., Toxicity of the zoanthid Palythoa tuberculosa (1972) Toxicon., 10, pp. 611-617Kramarsky, E.W., Fine, M., Loya, Y., Coral polyp expulsion (1997) Nature, 387, p. 137Larson, K.S., Larson, R.J., On the ecology of Isaurus duchassaingi (Cnidaria: Zoanthidea) from South Water Cay, Belize (1982) The Atlantic Barrier Reef Ecosystem at Carrie Bow Cay Belize, pp. 475-488. , K. Rutzler and I.G. Macintyre, eds. Smithsonian Contrib. Mar. Sci, Washington D.CLasker, H.R., Vegetative reproduction in the octocoral Briareum asbestinum (1983) J. Exp. Mar. Ecol., 72, pp. 157-169Clonal propagation and population dynamics of a gorgonian coral (1990) Ecology, 71, pp. 1578-1589Levins, R., (1968) Evolution in Changing Environments, 120p. , Princeton University Press, PrincetonMcFadden, C.S., Colony fission increases particle capture rates of a soft coral: Advantages of being a small colony (1986) J. Exp. Mar. Biol. Ecol., 103, pp. 1-20A comparative demographic analysis of clonal reproduction in a temperate soft coral (1991) Ecology, 72, pp. 1849-1866Migotto, A.E., Anthozoan bleaching on the southeastern coast of Brazil in the summer of 1994 (1997) Proc. 6th Conf. on Coelenterate Biology, pp. 329-335p. , AmsterdamMinasian, L.L., Characteristics of asexual reproduction in the sea anemone Haliplanella luciae reared in the laboratory (1976) Coelenterate Ecology and Behavior, pp. 289-298. , G.O. Mackie, ed. Plenum Press, New YorkThe effect of exogenous factors on morphology and asexual reproduction in laboratory cultures of the intertidal sea anemone, Haliplanella luciae (Verrill) (Anthozoa: Actiniaria) from Delaware (1979) J. Exp. Mar. Biol. Ecol., 40, pp. 235-246The relationship of size and biomass to fission rate in a clone of the sea Anemone, Haliplanella luciae (Verril) (1982) J. Exp. Mar. Biol. Ecol., 58, pp. 151-162Mariscal, R.N., Characteristics and regulation of fission activity in clonal cultures of the cosmopolitan sea anemone, Haliplanella luciae (1979) Biol. Bull., 157, pp. 478-493Mladenov, P.V., Environmental factors influencing asexual reproductive processes in echinoderms (1996) Oceanol. Acta, 19, pp. 227-235Muirhead, A., Ryland, J.S., A review of the genus Isaurus (Zoanthidea) including new records from Fiji (1985) J. Nat. Hist., 19, pp. 323-335Newell, S.J., Solbrig, O.T., Kincaid, D.T., Studies on the population biology of the genus Viola III the demography of Viola blanda and Viola pallens (1981) J. Ecol., 69, pp. 997-1016Okamura, B., The effects of ambient flow velocity, colony size, and upstream colonies on the feeding success of Bryozoa. II. Conopeum reticulum, an encrusting species (1985) J. Exp. Mar. Biol. Ecol., 89, pp. 69-80Oliver, J.S., Selection for asexual reproduction in an Antarctic polychaete worm (1984) Mar. Ecol. Prog. Ser., 19, pp. 33-38Ottesen, P.O., Lucas, J.S., Divide or broadcast: Interrelation of asexual and sexual reproduction in a population of the fissiparous hermaphroditic seastar Nepanthia belcheri (Asteroidea: Asterinidae) (1982) Mar. Biol., 69, pp. 223-233Pastorok, R.A., Bilyard, G.R., Effects of sewage pollution on coral-reef communities (1985) Mar. Ecol. Prog. Ser., 21, pp. 175-189Rocha, L.A., Bowen, B.W., Assessment of cryptic reef fish species in Brazil using molecular markers (2000) Proc. 9th Int. Coral Reef Symp., p. 21. , Bali. AbstractRogers, C.S., Responses of coral reefs and reef organisms to sedimentation (1990) Mar. Ecol. Prog. Ser., 62, pp. 185-202Rosen, B.R., Taylor, J.D., Reef coral from Aldabra: New mode of reproduction (1969) Science, 166, pp. 119-120Ryland, J.S., Reproduction in Zoanthidea (Anthozoa: Hexacorallia) (1997) Invertebr. Reprod. Dev., 31, pp. 177-188Warner, G.F., Growth and form in modular animals: Ideas on the size and arrangement of zooids (1986) Phil. Trans. R. Soc. Lond. B., 313, pp. 53-76Sammarco, P.W., Polyp bail-out: An escape response to environmental stress and a new means of reproduction in corals (1982) Mar. Ecol. Prog. Ser., 10, pp. 57-65Scheer, G., Die formenvielfalt der riffkorallen (1959) Bericht 1958/1959 Naturwissenschaften Verein Dormstadt, 50, pp. 50-67Schmidt, H., Anthopleura stellula (Actiniaria, Actiniidae) and its reproduction by transverse fission (1970) Mar. Biol., 5, pp. 245-255Sebens, K.P., The energetics of asexual reproduction and colony formation in benthic marine invertebrates (1979) Am. Zool., 19, pp. 683-697The regulation of asexual reproduction and indeterminate body size in the sea anemone Anthopleura elegantissima (Brandt) (1980) Biol. Bull., 158, pp. 370-382Intertidal distribution of zoanthids on the Caribbean coast of Panama: Effects of predation and desiccation (1982) Bull. Mar. Sci., 32, pp. 316-335The limits to indeterminate growth: An optimal size variant applied to passive suspension feeders (1982) Ecology, 63, pp. 209-222Shick, J.M., Ecological physiology and genetics of the colonizing actinian Haliplanella luciae (1976) Coelenterate Ecology and Behavior, pp. 137-146. , G.O. Mackie, ed. Plenum Press, New York(1991) A Functional Biology of Sea Anemones, 424p. , Chapman & Hall, New YorkHoffmann, R.J., Effects of the trophic and physical environments on asexual reproduction and body size in the sea anemone Metridium senile (1980) Developmental and Cellular Biology of Coelenterates, pp. 211-216. , P. Tardent and R. Tardent, eds. NorthHolland Biomedical Press, New YorkShostak, S., 2. Cnidaria (1993) Reproductive Biology of Invertebrates. VI. Asexual Propagation and Reproductive Strategies, pp. 45-104. , K.G. Adiyodi and R.G. Adiyodi, eds. John Wiley & Sons, New YorkSmith, N., Lenhoff, M., Regulation of frequency of pedal laceration in a sea anemone (1976) Coelenterate Ecology and Behavior, pp. 117-125. , G.O. Mackie, ed. Plenum Press, New YorkSoong, K., Shiau, Y.S., Chen, C.P., Morphological and reproductive variations of the zoanthid, Sphenopus marsupialis, from two locations in Taiwan (1995) Proc. 6th Int. Conf. Coelenterate Biol., 91p. , AmsterdamMorphological and life history divergence of the zoanthid, Sphenopus marsupialis off the Taiwanese coast (1999) Zool. Stud., 38, pp. 333-343Sokal, R.R., Rohlf, F.J., (1995) Biometry, 887p. , W.H. Freeman and Co., New YorkSteen, R.G., Muscatine, L., Daily budgets of photosynthetically fixed carbon in symbiotic zoanthids (1984) Biol. Bull., 167, pp. 477-487Stoner, D.S., Fragmentation: A mechanism for the stimulation of genet growth rates in an encrusting colonial ascidian (1989) Bull. Mar. Sci., 45, pp. 277-287Suchanek, T.H., Green, D.J., Interspecific competition between Palythoa caribaeorum and other sessile invertebrates on St.Croix reefs, US Virgin Islands (1981) Proc. 4th Int. Coral Reef Symp., 2, pp. 679-684. , ManilaTanner, J.E., The effects of density on the zoanthid Palythoa caesia (1997) J. Anim. Ecol., 66, pp. 793-810Density-dependent population dynamics in clonal organisms: A modeling approach (1999) J. Anim. Ecol., 68, pp. 390-399Tun, K.P.P., Cheshire, A.C., Chou, L.M., Twenty-four hour in situ monitoring of oxygen production and respiration of the colonial zoanthid Palythoa (1997) Environ. Monit. Assess., 44, pp. 33-43Vaughan, T.W., Wells, J.W., (1943) Revision of the Suborders Families, and Genera of the Scleractinia, 363p. , Geol. Soc. of America, BaltimoreVerrill, A.E., Notes in radiata. Review of the corals and polyps of the west coast of America (1869) Trans. Connect. Acad., 1, pp. 1868-1870Walker, T.A., Bull, G.D., A newly discovered method of reproduction in gorgonian coral (1983) Mar. Ecol. Prog. Ser., 12, pp. 137-143Williams, G.C., (1975) Sex and Evolution, 210p. , Princeton University Press, PrincetonWulff, J.L., Dispersal and survival of fragments of coral reef sponges (1985) Proc. 5th Int. Coral Reef Congr., 5, pp. 119-124. , TahitiYamazato, K., Yoshimoto, F., Yoshihara, N., Reproductive cycle of a Zoanthid, Palythoa tuberculosa (Esper) (1973) Publ. Seto. Mar. Biol. Lab., 20, pp. 275-283Isa, T., Dynamics of colonial growth in a zoanthid, Palythoa tuberculosa (Esper) (1981) Proc. 4th Int. Coral Reef Symp., 2, 760p. , Manil

    Cardiac end vascular responses of isolated rat tissues treated with diterpenes from Sinularia flexibilis (Coelenterata: Octocorallia)

    No full text
    The marine environment is a rich source of compounds with cardiovascular activity. This study characterizes the cardiac and vascular responses in isolated rat tissues of flexibilide, dihydroflexibilide and sinulariolide, three diterpenes isolated from the soft coral Sinularia flexibilis. On rat left ventricular papillary muscles, dihydroflexibilide and flexibilide showed similar potencies (- log EC = 4.69 ± 0.05 and 4.66 ± 0.06, respectively); the maximal response to dihydroflexibilide of 1.4 ± 0.2 mN was 35 ± 7% that of calcium chloride in the same muscles. All diterpenes relaxed rat thoracic aortic rings precontracted with KCl (100 mM) with similar potencies (flexibilide, - log EC = 4.17 ± 0.06). Flexibilide was further characterized and shown to increase force in isolated rat left atria by 0.8 ± 0.5 mN at 1 x 10 M, to increase rate of contraction in isolated rat right atria by 18 ± 5 beats/min at 3 x 10 M and to completely relax endothelium-denuded rat thoracic aortic rings ( - log EC) = 4.14 ± 0.05). Toxicity as indicated by the occurrence of ectopic beats was not observed with the diterpenes at concentrations which produced complete relaxation of blood vessels, maximal positive inotropic activity and minor positive chronotropic responses. Thus, these compounds may be useful lead compounds in the search for improved treatment of cardiovascular disease, especially heart failure

    Potencial atrator de peixes ósseos em recife artificial no litoral norte do estado do Rio de Janeiro, Brasil Attractor potential of osteichthyes in artificial reef on the northern coast of Rio de Janeiro State, Brazil

    No full text
    <abstract language="eng">Artificial reefs have become an important and popular resource enhancement technique by concentrating fishes and by increasing natural production of biological resources. In order to increase the necto-benthic colonization potencial, an artificial reef was installed on the northern coast of Rio de Janeiro (21º27'S, 41ºOO'W), an area with typically low relief bottom. Measuring nearly 1500 m², the reef consisted of four sets of different materials randomly disposed: concrete pipes (N = 12); tires structures (N = 20); and cement tanks (N = 7) and pre-made blocks (N = 4). ln order to determine the artificial reef effects on the teleost community, trammel nets were used for monthly sampling the reef site (RA) and on a control area (AC) with sandy bottom. During the 23-month survey from April/96 to March/98, were recorded: a) Chaetodipterus faber (Broussonet, 1782) and Haemulon aurolieatum (Cuvier, 1829) as exclusive species of the RA; b) higher values of species richness and abundance on the RA, at least in 5 of 8 periods; c) increase on the fish abundance on summer months. Correlation analysis indicated that salinity and precipitation were the most significant environmental factors correlated with the temporal fish community variation. This results highlight the importance of rainfall periodicity and the influence of Paraíba do Sul River on the nekton assemblage distribution. It is suggested that the functional role of the artificial reef might be related to higher availability of local shelter and food resources
    corecore