Marine Biology

, Volume 161, Issue 9, pp 2079–2095 | Cite as

Size, spatial, and bathymetrical distribution of the ascidian Halocynthia papillosa in Mediterranean coastal bottoms: benthic–pelagic coupling implications

Original Paper

Abstract

Benthic suspension feeders are abundant in Mediterranean coastal environments, though most of them are threatened due to overexploitation, climate change impacts, and unregulated diving or fishing practices. Little is known about most of the coastal communities in terms of large-scale distribution and realistic benthic–pelagic coupling implications, which are keys to understand and manage those threatened ecosystems. The active suspension feeder Halocynthia papillosa (one of the most common ascidian species of the Mediterranean Sea) was selected as a model organism to help to understand the ecological role in benthic–pelagic coupling processes and its importance as a carbon sink (an essential ecosystem service). The spatial and bathymetrical distribution of this organism has been studied using remotely operated vehicle video transects. The species was distributed throughout the study area, with a maximum density of 4 specimens m−2. The highest abundances and the biggest sizes were observed on the range of 20–50 m depth. The role as carbon and nitrogen sink of this suspension feeder has been quantified coupling distribution data with existing in situ studies of feeding and respiration. Along the 1.24 ha of the study area, H. papillosa yearly ingested 519.4 g C and 31.4 g N and retained 20.2 g C. As long as the physiological data are known, this new methodology could be very useful in assessing bentho–pelagic links and the capacity of being C and N sinks of a wide range of species. This new approach may be essential for the future management of benthic communities.

References

  1. Ambroso S, Gori A, Dominguez-Carrió C, Gili JM, Berganzo E, Teixidó N, Greenacre M, Rossi S (2013) Spatial distribution patterns of the soft corals Alcyonium acaule and Alcyonium palmatum in coastal bottoms (Cap de Creus, northwestern Mediterranean Sea). Mar Biol. doi:10.1007/s00227-013-2295-4 Google Scholar
  2. Anscombe FJ, Glynn WJ (1983) Distribution of kurtosis statistic for normal statistics. Biometrika 70:227–234Google Scholar
  3. Armsworthy SL, MacDonald BA, Ward JE (2001) Feeding activity, absorption efficiency and suspension feeding processes in the ascidian, Halocynthia pyriformis (Stolidobranchia: Ascidiacea): responses to variations in diet quantity and quality. J Exp Mar Biol Ecol 260:41–69CrossRefGoogle Scholar
  4. Becerro MA, Turon X (1992) Reproductive cycles of the ascidians Microcosmus sabatieri and Halocynthia papillosa in the Northwestern Mediterranean. PSZN I: Mar Ecol 13:363–373Google Scholar
  5. Best BA (1988) Passive suspension feeding in a sea pen: effects of ambient flow on volume flow rate and filtering efficiency. Biol Bull 175:332–342CrossRefGoogle Scholar
  6. Bianchi CN, Pronzato R, Cattaneo-Vietti R, Benedetti Cecchi L, Morri C, Pansini M, Chemello R, Milazzo M, Fraschetti S, Terlizzi A, Peirano A, Salvati E, Benzoni F, Calcinai B, Cerrano C, Bavestrello G (2004) Hard bottoms. Biol Mar Mediterr 11:185–215Google Scholar
  7. Bianchi CN, Parravicini V, Montefalcone M, Rovere A, Morri C (2012) The challenge of managing marine biodiversity: a practical toolkit for a cartographic, territorial approach. Diversity 4:419–452CrossRefGoogle Scholar
  8. Bo M, Bertolino M, Borghini M, Castellano M, Harriague AC, Di Camillo CG, Gasparini GP, Misic C, Povero P, Pusceddu A, Schroeder K, Bavestrello G (2011) Characteristics of the mesophotic megabenthic assemblages of the Vercelli seamount (North Tyrrhenian Sea). PLoS ONE 6:e16357CrossRefGoogle Scholar
  9. Bongaerts P, Ridgway T, Sampayo EM, Hoegh-Guldberg O (2010) Assessing the ‘deep reef refugia’ hypothesis: focus on Caribbean reefs. Coral Reefs 29:309–327CrossRefGoogle Scholar
  10. Bridge T, Guinotte J (2013) Mesophotic coral reef ecosystems in the Great Barrier Reef world heritage area: their potential distribution and possible role as refugia from disturbance. Research Publication no. 109, Great Barrier Reef Marine Park Authority, TownsvilleGoogle Scholar
  11. Cavaletto JF, Gardner WS (1999) Seasonal dynamics of lipids in freshwater benthic invertebrates. In: Arts M, Wainman B (eds) Lipids in freshwater ecosystems. Springer, New York, pp 109–131CrossRefGoogle Scholar
  12. Coma R, Ribes M, Gili JM, Hughes RN (2001) The ultimate opportunists: consumers of seston. Mar Ecol Prog Ser 219:305–308CrossRefGoogle Scholar
  13. Coma R, Ribes M, Gili JM, Zabala M (2002) Seasonality of in situ respiration rate in three temperate benthic suspension feeders. Limnol Oceanogr 47:324–331CrossRefGoogle Scholar
  14. Coma R, Pola E, Ribes M, Zabala M (2004) Long-term assessment of a temperate octocoral mortality patterns, protected vs. unprotected areas. Ecol Appl 14:1466–1478CrossRefGoogle Scholar
  15. Cúrdia J, Monteiro P, Afonso CM, Santos MN, Cunha MR, Gonçalves JM (2013) Spatial and depth-associated distribution patterns of shallow gorgonians in the Algarve coast (Portugal, NE Atlantic). Helgol Mar Res. doi:10.1007/s10152-012-0340-1
  16. DeGeest AL, Mullenbach BL, Puig P, Nittrouer CA, Drexler TM, Durrieu de Madron X, Orange DL (2008) Sediment accumulation in the western Gulf of Lions, France: the role of Cap de Creus canyon in linking shelf and slope sediment dispersal systems. Cont Shelf Res 28:2031–2047CrossRefGoogle Scholar
  17. Di Camillo CG, Giordano G, Bo M, Betti F, Mori M, Puce S, Bavestrello G (2013) Seasonal patterns in the abundance of Ectopleura crocea (Cnidaria: Hydrozoa) on a shipwreck in the Northern Adriatic. Mar Ecol 34:25–32CrossRefGoogle Scholar
  18. Duarte CM, Marbà N, Gacia E, Fourqurean JW, Beggins J, Barrón C, Apostolaki ET (2010) Seagrass community metabolism: assessing the carbon sink capacity of seagrass meadows. Glob Biogeochem Cy. doi:10.1029/2010GB003793
  19. Durrieu de Madron X, Abassi A, Heussner S, Monaco A, Aloisi JC, Radakovitch O, Giresse P, Buscail R, Kerherve P (2000) Particulate matter and organic carbon budgets for the Gulf of Lions (NW Mediterranean). Oceanol Acta 23:717–730CrossRefGoogle Scholar
  20. Elias-Piera F, Rossi S, Gili JM, Orejas C (2013) Trophic ecology of seven Antarctic gorgonian species. Mar Ecol Prog Ser 477:93–106CrossRefGoogle Scholar
  21. Eong OJ (1993) Mangrove—a carbon source and sink. Chemosphere 27:1097–1107CrossRefGoogle Scholar
  22. Estrada M (1996) Primary production in the northwestern Mediterranean. Sci Mar 60:55–64Google Scholar
  23. Fiorillo I, Rossi S, Alva V, Gili JM, López-González PJ (2013) Seasonal cycle of sexual reproduction of the Mediterranean soft coral Alcyonium acaule (Anthozoa, Octocorallia). Mar Biol 160:719–728CrossRefGoogle Scholar
  24. Fisher TR (1976) Oxygen uptake of the solitary tunicate Styela plicata. Biol Bull 151:297–305CrossRefGoogle Scholar
  25. Fletcher LM, Forrest BM, Bell JJ (2013) Natural dispersal mechanisms and dispersal potential of the invasive ascidian Didemnum vexillum. Biol Invasions. doi:10.1007/s10530-012-0314-x Google Scholar
  26. García-Rubies A, Zabala M (1990) Effects of total fishing prohibition on the rocky fish assemblages of Medes Islands marine reserve (NW Mediterranean). Sci Mar 54:317–328Google Scholar
  27. Garcia-Rubies A, Mateo MA, Hereu B, Coma R, Teixidó N, Garrabou J, Serrano E (2009) Preliminary assessment of the impact of an extreme storm on catalan Mediterranean benthic communities. In: 11th Plinius Conference on Mediterranean Storms. Barcelona, Spain, pp 7–11Google Scholar
  28. Garrabou J, Ballesteros E, Zabala M (2002) Structure and dynamics of north-western Mediterranean rocky benthic communities along a depth gradient. Estuar Coast Shelf Sci 55:493–508CrossRefGoogle Scholar
  29. Gili JM, Ballesteros E (1991) Structure of cnidarian populations in Mediterranean sublittoral communities as a result of adaptation to different environmental conditions. Oecol Aquat 10:243–254Google Scholar
  30. Gili JM, Coma R (1998) Benthic suspension feeders: their paramount role in littoral marine food webs. Trends Ecol Evol 13:316–321CrossRefGoogle Scholar
  31. Gili JM, Ros J (1985) Study and cartography of the benthic communities of Medes Islands (NE Spain). PSZN I: Mar Ecol 6:219–238Google Scholar
  32. Gili JM, Coma R, Orejas C, López-Gonzáles PJ, Zabala M (2001) Are Antarctic suspension-feeding different from those elsewhere in the world? Polar Biol 24:473–485CrossRefGoogle Scholar
  33. Gori A, Rossi S, Berganzo E, Pretus JL, Dale MRT, Gili JM (2011a) Spatial distribution patterns of the gorgonians Eunicella singularis, Paramuricea clavata, and Leptogorgia sarmentosa (Cap of Creus, northwestern Mediterranean Sea). Mar Biol 158:143–158CrossRefGoogle Scholar
  34. Gori A, Rossi S, Linares C, Berganzo E, Orejas C, Dale MR, Gili JM (2011b) Size and spatial structure in deep versus shallow populations of the Mediterranean gorgonian Eunicella singularis (Cap de Creus, northwestern Mediterranean Sea). Mar Biol 158:1721–1732CrossRefGoogle Scholar
  35. Gori A, Viladrich N, Gili JM, Kotta M, Cucio C, Magni L, Bramanti L, Rossi S (2012) Reproductive cycle and trophic ecology in deep versus shallow populations of the Mediterranean gorgonian Eunicella singularis (Cap de Creus, northwestern Mediterranean Sea). Coral Reefs 31:823–837CrossRefGoogle Scholar
  36. Graf G (1992) Benthic–pelagic coupling: a benthic view. Oceanogr Mar Biol 30:149–190Google Scholar
  37. Grèmare A, Amouroux JM, Charles F, Dinet A, Riaux-Gobin C, Baudart J, Medernach L, Bodiou JY, Vétion G, Colomines JC, Albert P (1997) Temporal changes in the biochemical composition and nutritional value of the particulate organic matter available to surface deposit-feeders: a two year study. Mar Ecol Prog Ser 150:195–206CrossRefGoogle Scholar
  38. Henry LA, Roberts JM (2007) Biodiversity and ecological composition of macrobenthos on cold-water coral mounds and adjacent off-mound habitat in the bathyal Porcupine Seabight, NE Atlantic. Deep-Sea Res Part I 54:654–672CrossRefGoogle Scholar
  39. Hereu B, Rodríguez A, Linares Prats C, Díaz Viñolas D, Riera JL, Zabala M (2010) Cartografia bionòmica del litoral submergit de la costa del Montgrí. Technical report (in catalan) for Departament d’Agricultura, Ramaderia, Pesca, Alimentació i Medi Natural de la Generalitat de CatalunyaGoogle Scholar
  40. Hily C (1991) Is the activity of benthic suspension feeders a factor controlling water quality in the bay of Brest? Mar Ecol Prog Ser 69:179–188CrossRefGoogle Scholar
  41. Jiang AL, Jian L, Wang CH (2008) Physiological energetics of the ascidian Styela clava in relation to body size and temperature. Comp Biochem Phys A 149:129–136CrossRefGoogle Scholar
  42. Jones CG, Lawton JH, Shachak M (1994) Organisms as ecosystem engineers. Oikos 69:373–386CrossRefGoogle Scholar
  43. Kinsey DW, Hopley D (1991) The significance of coral reefs as global carbon sinks—response to greenhouse. Palaeogeogr Palaeoclimatol 89:363–377CrossRefGoogle Scholar
  44. Klumpp DW (1984) Nutritional ecology of the ascidian Pyura stolonifera: influence of body size, food quantity and quality on filter-feeding, respiration, assimilation efficiency and energy balance. Mar Ecol Prog Ser 19:269–284CrossRefGoogle Scholar
  45. Komsta L, Novomestky F (2012) Moments: moments, cumulants, skewness, kurtosis and related tests. R Package Version 0.12Google Scholar
  46. Krieger KJ, Wing BL (2002) Megafauna associations with deepwater corals (Primnoa spp.) in the Gulf of Alaska. Hydrobiologia 471:83–90CrossRefGoogle Scholar
  47. Lampert W (1984) The measurement of respiration. A manual on methods for the assessment of secondary production in fresh waters. Blackwell Scientific, Oxford, pp 413–468Google Scholar
  48. Leicher JJ, Witman JD (1997) Water flow over subtidal rock walls: relation to distributions and growth rates of sessile suspension feeders in the Gulf of Maine. Water flow and growth rate. J Exp Mar Biol Ecol 209:293–307CrossRefGoogle Scholar
  49. Lesser MP (2006) Benthic–pelagic coupling on coral reefs: feeding and growth of Caribbean sponges. J Exp Mar Biol Ecol 328:277–288CrossRefGoogle Scholar
  50. Linares C, Garrabou J, Hereu B, Diaz D, Marschal C, Sala E, Zabala M (2012) Assessing the effectiveness of marine reserves on unsustainably harvested long-lived sessile invertebrates. Conserv Biol 26:88–96CrossRefGoogle Scholar
  51. Loo LO, Rosemberg R (1989) Bivalve suspension-feeding dynamics and benthic–pelagic coupling in an eutrophicated bay. J Exp Mar Biol Ecol 130:253–276CrossRefGoogle Scholar
  52. Lübbering B, Giraud-Guille MM, Goffinet G (1993) Tunic morphogenesis in the sea peach (Halocynthia papillosa, Ascidiacea, Urochordata): cellular events, the initiation of twisted fibrous arrangements and spine formation. Biol Cell 79:167–176CrossRefGoogle Scholar
  53. Luna-Pérez B, Valle C, Vega Fernández T, Sanchez-Lizaso JL, Ramos-Espla AA (2010) Halocynthia papillosa (Linnaeus, 1767) as an indicator of SCUBA diving impact. Ecol Ind 10:1017–1024CrossRefGoogle Scholar
  54. Markus JA, Lambert CC (1983) Urea and ammonia excretion by solitary ascidians. J Exp Mar Biol Ecol 66:1–10CrossRefGoogle Scholar
  55. Martinez Ricart A (2011) Revisió de la cartografia bionòmica de la Reserva Marina de les Illes Medes i estudi dels canvis a llarg termini de les comunitats de macrobentos. Master Thesis of the University of Barcelona (in catalán), 38 ppGoogle Scholar
  56. McClintock JB, Heine J, Slattery M, Weston J (1991) Biochemical and energetic composition, population biology, and chemical defense of the Antarctic ascidian Cnemidocarpa verrucosa lesson. J Exp Mar Biol Ecol 147:163–175CrossRefGoogle Scholar
  57. Mortensen PB, Buhl-Mortensen L (2004) Distribution of deep-water gorgonian corals in relation to benthic habitat features in the Northeast Channel (Atlantic Canada). Mar Biol 144:1223–1238CrossRefGoogle Scholar
  58. Naranjo SA, Carballo JL, García-Gómez JC (1996) Effects of environmental stress on ascidian populations in Algeciras Bay (Southern Spain). Possible marine bioindicators? Mar Ecol Prog Ser 144:119–131CrossRefGoogle Scholar
  59. Navarro L, Ballesteros E, Linares C, Hereu B (2011) Spatial and temporal variability of deep-water algal assemblages in the Northwestern Mediterranean: the effects of an exceptional storm. Estuar Coast Shelf Sci 95:52–58CrossRefGoogle Scholar
  60. Officer CB, Smayda TJ, Mann R (1982) Benthic filter feeding: a natural eutrophication control. Mar Ecol Prog Ser 9:203–210CrossRefGoogle Scholar
  61. Orejas C, Gori A, Lo Iacono C, Puig P, Gili JM, Dale MRT (2009) Cold-water corals in the Cap de Creus canyon, northwestern Mediterranean: spatial distribution, density and anthropogenic impact. Mar Ecol Prog Ser 397:37–51CrossRefGoogle Scholar
  62. Palanques A, Durrieu de Madron X, Puig P, Fabres J, Guillén J, Calafat A, Canals M, Heussner S, Bonnin J (2006) Suspended sediment fluxes and transport processes in the Gulf of Lions submarine canyons. The role of storms and dense water cascading. Mar Geol 234:43–61CrossRefGoogle Scholar
  63. Pascual J, Flos J (1984) Meteorologia i oceanografia. In: Ros JD, Olivella I, Gili JM (eds) Els sistemes naturals de les illes Medes. Institut d’Estudis Catalans, pp 75–114Google Scholar
  64. Petersen JK (2007) Ascidians suspension feeding. J Exp Mar Biol Ecol 342:127–137CrossRefGoogle Scholar
  65. Petersen JK, Riisgård HU (1992) Filtration capacity of the ascidian Ciona intestinalis and its grazing impact in a shallow fjord. Mar Ecol Prog Ser 88:9–17CrossRefGoogle Scholar
  66. Quantum GIS Development Team (2009) GNU General Public License. http://qgis.osgeo.org
  67. R Development Core Team (2012) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0. http://www.R-project.org
  68. Ribes M, Coma R, Gili JM (1998) Seasonal variation of in situ feeding rates by the temperate ascidian Halocynthia papillosa. Mar Ecol Prog Ser 175:201–213CrossRefGoogle Scholar
  69. Ribes M, Coma R, Gili JM (1999) Seasonal variation of particulate organic carbon, dissolved organic carbon and the contribution of microbial communities to the live particulate organic carbon in a shallow near-bottom ecosystem at the northwestern Mediterranean Sea. J Plankton Res 21:1077–1100CrossRefGoogle Scholar
  70. Riisgård HU, Larsen PS (2000) Comparative ecophysiology of active zoobenthic filter feeding, essence of current knowledge. J Sea Res 44:169–193CrossRefGoogle Scholar
  71. Riisgård HU, Bondo Christensen P, Olesen NJ, Petersen JK, Møller MM, Andersen P (1995) Biological structure in a shallow cove (Kertinge Nor, Denmark)—control by benthic nutrient fluxes and suspension-feeding ascidians and jellyfish. Ophelia 41:329–344Google Scholar
  72. Rius M, Zabala M (2008) Are marine protected areas useful for the recovery of the Mediterranean mussel populations? Aquat Conserv: Mar Freshw Ecosyst 18:527–540CrossRefGoogle Scholar
  73. Robbins IJ (1983) The effects of body size, temperature, and suspension density on the filtration and ingestion of inorganic particulate suspensions by ascidians. J Exp Mar Biol Ecol 70:65–78CrossRefGoogle Scholar
  74. Rossi S (2013) The destruction of the ‘animal forests’ in the oceans: towards an over-simplification of the benthic ecosystems. Ocean Coast Manage 84:77–85CrossRefGoogle Scholar
  75. Rossi S, Gili JM (2005) Composition and temporal variation of the near-bottom seston in a Mediterranean coastal area. Estuar Coast Shelf Sci 65:385–395CrossRefGoogle Scholar
  76. Rossi S, Grémare A, Gili JM, Amouroux JM, Jordana E, Vétion G (2003) Biochemical characteristics of settling particulate organic matter at two north-western Mediterranean sites: a seasonal comparison. Estuar Coast Shelf Sci 58:423–434CrossRefGoogle Scholar
  77. Rossi S, Gili JM, Coma R, Linares C, Gori A, Vert N (2006) Temporal variation in protein, carbohydrate, and lipid concentrations in Paramuricea clavata (Anthozoa, Octocorallia): evidence for summer–autumn feeding constraints. Mar Biol 149:643–651CrossRefGoogle Scholar
  78. Rossi S, Tsounis G, Orejas C, Padrón T, Gili JM, Bramanti L, Teixidó N, Gutt J (2008) Survey of deep-dwelling red coral (Corallium rubrum) populations at Cap de Creus (NW Mediterranean). Mar Biol 154:533–545CrossRefGoogle Scholar
  79. Rossi S, Bramanti L, Broglio E, Gili JM (2012) Trophic impact of long-lived species indicated by population dynamics in the short-lived hydrozoan Eudendrium racemosum. Mar Ecol Prog Ser 467:97–111CrossRefGoogle Scholar
  80. Sala E, Garrabou J, Zabala M (1996) Effects of diver frequentation on Mediterranean sublittoral populations of the bryozoan Pentapora fascialis. Mar Biol 126:451–459CrossRefGoogle Scholar
  81. Sala E, Boudouresque CF, Harmelin-Vivien M (1998) Fishing, trophic cascades, and the structure of algal assemblages: evaluation of an old but untested paradigm. Oikos 82:425–439CrossRefGoogle Scholar
  82. Santangelo G, Bramanti L, Rossi S, Tsounis G, Vielmini I, Lott C, Gili JM (2012) Patterns of variation in recruitment and post-recruitment processes of the Mediterranean precious gorgonian coral Corallium rubrum. J Exp Mar Biol Ecol 411:7–13CrossRefGoogle Scholar
  83. Sardá R, Rossi S, Martí X, Gili JM (2012) Marine benthic cartography of the Cap de Creus (NE Catalan Coast, Mediterranean Sea). Sci Mar 76:159–171CrossRefGoogle Scholar
  84. Schols P, Smets E (2001) Carnoy: analysis software for LM, SEM and TEM images. Leuven: distributed by the author. http://www.carnoy.org
  85. Shenkar N, Loya L (2008) The solitary ascidian Herdmania momus: native (Red Sea) versus non-indigenous (Mediterranean) populations. Biol Invasion 10:1431–1439CrossRefGoogle Scholar
  86. Shimeta J, Jumars PA (1991) Physical mechanisms and rates of particle capture by suspension feeders. Oceanogr Mar Biol 29:191–257Google Scholar
  87. Smith SV (1981) Macrophythes as a global carbon sink. Science 211:838–840CrossRefGoogle Scholar
  88. Surfer 8 Software Online. http://www.goldensoftware.com. Accessed May 2006
  89. Teixidó N, Casas E, Cebrián E, Linares C, Garrabou J (2013) Impacts on coralligenous outcrop biodiversity of a dramatic coastal storm. PLoS ONE 8:e53742CrossRefGoogle Scholar
  90. Tsounis G, Rossi S, Gili JM, Arntz W (2006) Population structure of an exploited benthic cnidarian: the case study of red coral (Corallium rubrum L.). Mar Biol 149:1059–1070CrossRefGoogle Scholar
  91. Turon X (1985) Ascidias del Cabo de Creus (Costa NE española). Miscelanea Zoologica 9:265–271Google Scholar
  92. Turon X (1990) Distribution and abundance of ascidians from a locality on the Northeast Coast of Spain. Mar Ecol 11:291–308CrossRefGoogle Scholar
  93. Ulses C, Estournel C, Bonnin J, Durrieu de Madron X, Marsaleix P (2008) Impact of storms and dense water cascading on shelf-slope exchanges in the Gulf of Lion (NW Mediterranean). J Geophys Res: Oceans 113:C02010. doi:10.1029/2006JC003795 Google Scholar
  94. Weinberg S (1978) The minimal area problem in invertebrate communities of Mediterranean rocky substrata. Mar Biol 49:33–40CrossRefGoogle Scholar
  95. Wild C, Hoegh-Guldberg O, Naumann MS, Colombo-Pallotta MF, Ateweberhan M, Fitt WK, Iglesias-Prieto R, Palmer C, Bythell JC, Ortiz JC, Loya Y, van Woesik R (2011) Climate change impedes scleractinian corals as primary reef ecosystem engineers. Mar Freshw Res 62:205–215CrossRefGoogle Scholar
  96. Witman JD, Dayton PK (2000) Rocky subtidal communities. In: Bertness M, Gaines S, Hay M (eds) Marine community ecology. Sinauer, Sunderland, pp 339–366Google Scholar
  97. Young CM, Chia FS (1984) Microhabitat-associated variability in survival and growth of subtidal solitary ascidians during the first 21 days after settlement. Mar Biol 81:61–68CrossRefGoogle Scholar

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© Springer-Verlag Berlin Heidelberg 2014

Authors and Affiliations

  1. 1.Institut de Ciència i Tecnologia AmbientalsUniversitat Autònoma de BarcelonaCerdanyola del VallésSpain
  2. 2.Institut de Ciències del MarConsejo Superior de Investigaciónes CientificasBarcelonaSpain
  3. 3.Unidad de Sistemas Arrecifales, Instituto de Ciencias del Mar y LimnologíaUniversidad Nacional Autónoma de MexicoCancúnMexico

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