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Benthic biodiversity changes due to the opening of an artificial channel in a tropical coastal lagoon (Mexican Caribbean)

Published online by Cambridge University Press:  23 December 2010

Héctor A. Hernández-Arana  and
Brenda Ameneyro-Angeles
Héctor A. Hernández-Arana*
Affiliation:
El Colegio de la Frontera Sur, Unidad Chetumal, Departamento de Ecología Acuática y Sistemática, Avenida Centenario Km 5.5 CP 77900 Chetumal, Quintana Roo, México
Brenda Ameneyro-Angeles
Affiliation:
El Colegio de la Frontera Sur, Unidad Chetumal, Departamento de Ecología Acuática y Sistemática, Avenida Centenario Km 5.5 CP 77900 Chetumal, Quintana Roo, México
*
Correspondence should be addressed to: H.A. Hernández-Arana, El Colegio de la Frontera Sur, Unidad Chetumal, Departamento de Ecología Acuática y Sistemática, Avenida Centenario Km 5.5 CP 77900 Chetumal, Quintana Roo, México email: [email protected]
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Abstract

The construction of an artificial channel to a small embayment in the Chetumal Bay coastal lagoon complex, located on the Caribbean coast of Mexico, provided an opportunity to evaluate how large environmental changes influenced the structure of a low diversity benthic system. The objective of this study was to demonstrate that despite the absence of previous baseline information, the artificial channel has induced measurable changes in the biodiversity patterns of a hard substrata benthic community. The experimental design took into account the environmental setting influencing local benthic community structure and the sources of variability as a result of different substrate types and water depth. Four localities with ten replicates each were surveyed, and the presence/absence of macrobenthic biota species recorded during the rainy season. Our analysis using permutational multivariate analysis of variance indicated a significant increase in species richness in locations adjacent to the artificial channel. The highest species richness (66 species) was observed in the immediate area adjacent to the artificial channel and where exclusive species density was three to six times (18 exclusive species) than those present in other localities (6, 5 and 3 species) away from the channel. The presence of six species of hard corals indicated that the artificial channel offers a more suitable habitat for marine organisms colonizing the area than the natural channel. This study indicates the relative significance of confinement in structuring coastal lagoon benthic assemblages in tropical systems. Our results are similar to other findings underscoring the rate of colonization of marine organisms as a relevant process to explain benthic assemblage gradients and the importance of spatial–temporal interactions. The changes in species diversity caused by the artificial channel were clearly identified based on a sampling design that incorporated the main sources of environmental variability (distance to channels, substrate type and depth). Our study further demonstrates that changes in benthic community structure in the Chetumal Bay lagoon complex, as a result of human impacts, can be assessed even when community structure data before impact are absent.

Keywords

benthosenvironmental impactcoralscoastal lagoonsmultivariate analysisvariability
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 91 , Issue 5 , August 2011 , pp. 969 - 978
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

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References

REFERENCES

Anderson, M.J. (2001) A new method for non-parametric multivariate analysis of variance. Austral Ecology 26, 32–46.Google Scholar
Anderson, M.J. and Willis, T.J. (2003) Canonical analysis of principal coordinates: a useful method of constrained ordination for ecology. Ecology 84, 511–525.CrossRefGoogle Scholar
Anderson, M.J., Connell, S.D., Gillanders, B.M., Diebel, C.E., Blom, W.M., Saunders, J.E. and Landers, T.J. (2005) Relationships between taxonomic resolution and spatial scales of multivariate variation. Journal of Animal Ecology 74, 636–646.CrossRefGoogle Scholar
Anderson, M.J., Gorley, R.N. and Clarke, K.R. (2008) PERMANOVA + for PRIMER: guide to software and statistical methods. Plymouth: PRIMER-E.Google Scholar
Benedetti-Cecchi, L., Rindi, F., Bertocci, I., Bulleri, F. and Cinelli, F. (2001) Spatial variation in development of epibenthic assemblages in a coastal lagoon. Estuarine, Coastal and Shelf Science 52, 659–668.CrossRefGoogle Scholar
Carrillo, L., Palacios-Hernández, E., Yescas, M. and Ramírez Manguilar, A. (2009) Spatial and seasonal patterns of salinity in a large and shallow tropical estuary of the Western Caribbean. Estuaries and Coasts 32, 906–916.CrossRefGoogle Scholar
Clarke, K.R. and Warwick, R.M. (1998) Quantifying structural redundancy in ecological communities. Oecologia 113, 278–289.CrossRefGoogle ScholarPubMed
Clarke, K.R. and Gorley, R.N. (2006) PRIMER v6: user manual/tutorial. Plymouth: PRIMER-E.Google Scholar
Duarte, P., Macedo, M.F. and Fonseca, L.C. (2006) The relationship between phytoplankton diversity and community function in a coastal lagoon. Hydrobiologia 555, 3–18.CrossRefGoogle Scholar
Eberhardt, L.L. and Thomas, J.M. (1991) Designing environmental field studies. Ecological Monographs 61, 53–73.CrossRefGoogle Scholar
Espinoza-Avalos, J., Hernández-Arana, H.A., Álvarez-Legorreta, T., Quan-Young, L.I., Oliva-Rivera, J.J., Valdez-Hernández, M., Zavala-Mendoza, A., Cruz-Piñón, G., López, C.Y., Sepúlveda-Lozada, A., Worum-Ference, P., Villegas-Castillo, A. and Tussenbroek, B.I.V. (2009) Vegetación acuática sumergida. In Espinoza-Avalos, J., Islebe, G.A. and Hernández-Arana, H.A. (eds) El Sistema Ecológico Bahía de Chetumal/Corozal: Costa Occidental del Mar Caribe. Chetumal: El Colegio de la Frontera Sur.Google Scholar
Esteves, F.A., Caliman, A., Santangelo, J.M., Guariento, R.D., Farjalla, V.F. and Bozelli, R.L. (2008) Neotropical coastal lagoons: an appraisal of their biodiversity, functioning, threats and conservation management. Brazilian Journal of Biology 68, 967–981.CrossRefGoogle ScholarPubMed
Franco, A., Franzoi, P. and Torricelli, P. (2008) Structure and functioning of Mediterranean lagoon fish assemblages: a key for identification of water body types. Estuarine, Coastal and Shelf Science 79, 549–558.CrossRefGoogle Scholar
Frénod, E. and Goubert, E. (2007) A first step towards modelling confinement of paralic ecosystems. Ecological Modelling 200, 139–1148.CrossRefGoogle Scholar
Griffiths, S.P. (1999) Consequences of artificially opening coastal lagoons on their fish assemblages. International Journal of Salt Lake Research 8, 307–327.CrossRefGoogle Scholar
Guelorget, O., Gaujous, D., Louis, M. and Perthuisot, J.P. (1990) Macrobenthofauna of lagoons in Guadaloupean mangroves (Lesser Antilles): role and expressions of the confinement. Journal of Coastal Research 6, 611–626.Google Scholar
Harrington, L., Fabricius, K., De'Ath, G. and Negri, A. (2004) Recognition and selection of settlement substrata determine post-settlement survival in corals. Ecology 85, 3428–3437.CrossRefGoogle Scholar
Hewitt, J.E., Trush, S.E. and Cummings, V.J. (2001) Assessing environmental impacts: effects of spatial and temporal variability at likely impact scales. Ecological Applications 11, 1502–1516.CrossRefGoogle Scholar
Highsmith, R.C., Lueptow, R.L. and Schonberg, S.C. (1983) Growth and bioerosion of three massive corals on the Belize barrier reef. Marine Ecology Progress Series 13, 261–271.CrossRefGoogle Scholar
HP-Consultores-Ambientales (1999) Informe preventivo con formato de manifestación de impacto ambiental modalidad general: Continuación del proyecto de desazolve y terminación del canal de Zaragoza. S. D. G. d. M. Mercante. Mexico, Secretaria de Marina: 200.Google Scholar
Lai, P.C.C., Lee, W.H. and Wong, B.S.F. (2007) Construction of a drainage channel at Inner Deep Bay, Hong Kong: mitigating ecological and landscape impact through an environmentally friendly design. Landscape and Ecological Engineering 3, 179–185.CrossRefGoogle Scholar
Layman, C.A. (2003) Underwater visual census provides ‘snapshot’ assessment of tidal connectivity (Bahamas). Ecological Restoration 21, 132–133.Google Scholar
Lirman, D., Manzello, D. and Maciá, S. (2002) Back from the death: the resilience of Siderastrea radians to severe stress. Coral Reefs 21, 291–292.CrossRefGoogle Scholar
Mariani, S. (2001) Can spatial distribution of ichthyofauna describe marine influence on coastal lagoons? A central Mediterranean case study. Estuarine, Coastal and Shelf Science 52, 261–267.CrossRefGoogle Scholar
Mistri, M., Fano, E.A. and Rossi, R. (2001) Redundancy of macrobenthos from lagoonal habitats in the Adriatic Sea. Marine Ecology Progress Series 215, 289–296.CrossRefGoogle Scholar
Mumby, P.J. (2006) Connectivity of reef fish between mangroves and coral reefs: algorithms for the design of marine reserves at seascape scales. Biological Conservation 128, 215–222.CrossRefGoogle Scholar
Pérez-Ruzafa, A., Marcos-Diego, C. and Ros, J.D. (1991) Environmental changes related to recent human activities in the Mar Menor (SE of Spain). Marine Pollution Bulletin 23, 747–751.CrossRefGoogle Scholar
Pérez-Ruzafa, A.Quispe-Becerra, J.I., García-Charton, J.A. and Marcos, C. (2004) Composition, structure and distribution of the ichthyoplancton in a Mediterranean coastal lagoon. Journal of Fish Biology 64, 202–218.CrossRefGoogle Scholar
Pérez-Ruzafa, A., Fernández, A.I., Marcos, C., Gilabert, J.Quispe, J.I. and García-Charton, J.A. (2005) Spatial and temporal variations of hydrological conditions, nutrients, and chlorophyll a in a Mediterranean coastal lagoon (Mar Menor, Spain). Hydrobologia 550, 11–27.CrossRefGoogle Scholar
Pérez-Ruzafa, A., García-Charton, J.A. and Barcala, E., Marcos, C. (2006) Changes in benthic fish assemblages as a consequence of coastal works in a coastal lagoon. The Mar Menor (Spain, Western Mediterranean). Marine Pollution Bulletin 53, 107–120.CrossRefGoogle Scholar
Pérez-Ruzafa, A., Mompeán, M.C. and Marcos, C. (2007a) Hydrographic, geomorphologic, and fish assemblage relationships in coastal lagoons. Hydrobiologia 577, 107–125.CrossRefGoogle Scholar
Pérez-Ruzafa, A., Marcos, C., Pérez-Ruzafa, I.M., Barcala, E., Hegazi, M.I. and Quispe, J. (2007b) Detecting changes resulting from human pressure in a naturally quick-changing and heterogenous environment: spatial and temporal scales of variability in coastal lagoons. Estuarine, Coastal and Shelf Science 75, 175–188.CrossRefGoogle Scholar
Pérez-Ruzafa, A., Hegazi, M.I., Pérez-Ruzafa, I.M. and Marcos, C. (2008) Differences in spatial and seasonal patterns of macrophyte assemblages between a coastal lagoon and the open sea. Marine Environmental Research 5, 291–314.CrossRefGoogle Scholar
Quan-Young, L.I., Jiménez-Flores, S.G. and Espinoza-Ávalos, J. (2006) Flora béntica y reproducción de las algas Batophora spp. (Chlorophyta: Dasycladaceae) de una laguna costera contaminada (Bahía de Chetumal, México). Revista de Biologia Tropical 54, 341–355.CrossRefGoogle Scholar
Queiroz, N.C., Lima, F.P., Ribeiro, P.A., Pereira, S.G. and Santos, A.M. (2006) Using asymmetrical designs for environmental impact assessment of unplanned disturbances. Hydrobiologia 555, 223–227.CrossRefGoogle Scholar
Ruíz-Zarate, M.A. and Arias-González, J.E. (2004) Spatial study of juvenile corals in the northern region of the Mesoamerican Barrier Reef System (MBRS). Coral Reefs 23, 584–594.Google Scholar
Sale, P.F. and Kritzer, J.P. (2003) Determining the extent and spatial scale of population connectivity: decapods and coral reef fishes compared. Fisheries Research 65, 153–172.CrossRefGoogle Scholar
Sfriso, A., Facca, C. and Ghetti, P.F. (2003) Temporal and spatial changes of macroalgae and phytoplancton in a Mediterranean coastal area: the Venice lagoon as a case study. Marine Environmental Research 56, 617–636.CrossRefGoogle Scholar
Strathmann, R.R., Hughes, T.P., Kuris, A.M., Lindeman, K.C., Morgan, S.G., Pandolfi, J.M. and Warner, R.R. (2002) Evolution of local recruitment and its consequences for marine populations. Bulletin of Marine Science 70, 377–396.Google Scholar
Underwood, A.J. (1993) The mechanics of spatially replicated sampling programmes to detect environmental impacts in a variable world. Australian Journal of Ecology 18, 99–116.CrossRefGoogle Scholar
Underwood, A.J. (1994) On beyond BACI: sampling designs that might reliably detect environmental disturbance. Ecological Applications 4, 3–15.CrossRefGoogle Scholar
Underwood, A.J. (2000) Importance of experimental design in detecting and measuring stresses in marine populations. Journal of Aquatic Ecosystem Stress and Recovery 7, 3–24.CrossRefGoogle Scholar
Underwood, A.J., Chapman, M.G. and Roberts, D.E. (2003) A practical protocol to assess impacts of unplanned disturbance: a case study in Tuggerah Lakes Estuary, NSW. Ecological Management and Restoration 4, S4–S11.CrossRefGoogle Scholar
Vermeij, M.J.A., Frade, P.R., Jacinto, R.I.R., Debrot, A.O. and Bak, R.P.M. (2007) Effects of reproductive mode on habitat-related differences in the population structure of eight Caribbean coral species. Marine Ecology Progress Series 351, 91–102.CrossRefGoogle Scholar
Warwick, R.M. (1993) Environmental impact studies on marine communities: pragmatical considerations. Australian Journal of Ecology 18, 63–80.CrossRefGoogle Scholar
Wells, J.W. (1956) Scleractinia. In Moore, R.C. (ed.) Treatise on invertebrate paleontology. Kansas: Geological Society of America and University of Kansas Press, pp. F328–F443.Google Scholar
Wiens, J.A. and Parker, K.R. (1995) Analyzing the effects of accidental environmental impacts: approaches and assumptions. Ecological Applications 5, 1069–1083.CrossRefGoogle Scholar
Young, G.C. and Potter, I.C. (2003). Influence of an artificial entrance channel on the ichthyofauna of a large estuary. Marine Biology 142, 1181–1194.CrossRefGoogle Scholar