Feeding guild composition of a macrobenthic subtidal community along a depth gradient
DOI:
https://doi.org/10.3989/scimar.2009.73n2225Keywords:
macrobenthic community, feeding guilds, depth gradient, hydrodynamicsAbstract
The feeding guild composition of a macrobenthic community from southern Portugal was studied along a depth gradient (1.3 to 32 m). This gradient comprised shallow areas with severe physical stress and deeper areas with no significant hydrodynamic impact at the seafloor. The main goal was to determine the influence of the spatial and temporal differences of the hydrodynamic impact at the seafloor on the feeding guild composition of the macrobenthic community. The feeding guild composition changed gradually with depth, which reflects the differences in the hydrodynamics impact at the seafloor. Herbivores and sand-lickers dominated at the shallowest depths with fine sands, which correlated with higher levels of primary production. Scavengers were also distributed in the shallow areas, which was associated with the lower predation impact. Suspension feeders, in accordance with their physiological requirements, were distributed in coarser sands subjected to a physical impact. Carnivores, surface deposit feeders and sub-surface deposit feeders were distributed mainly below 8 m depth, where there was no significant impact from the wave climate. Carnivores were associated with coarser sands and were mainly small polychaetes and nemerteans. Sub-surface and surface deposit feeders were more abundant in the deepest areas of the depth gradient with fine sands and mud deposits with higher organic content. However, surface deposit feeders also occurred at shallower depths. Some seasonal differences related to disturbance impacts were found in the numerical dominance of the feeding guilds.
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References
Arruda, E.P., O. Domaneschi and A.C.Z. Amaral. – 2003. Mollusc feeding guilds on sandy beaches in São Paulo State, Brazil. Mar. Biol., 143: 691-701. doi:10.1007/s00227-003-1103-y
Best, M.A, A.W. Wither and S. Coates. – 2007. Dissolved oxygen as a physico-chemical supporting element in the Water Framework Directive. Mar. Poll. Bull., 55: 53-64. doi:10.1016/j.marpolbul.2006.08.037 PMid:17074369
Byrén, L., G. Ejdung and R. Elmgren. – 2002. Comparing rate and depth of feeding in benthic deposit-feeders: a test on two amphipods, Monoporeia affinis (Lindström) and Pontoporeia femorata Kröyer. J. Exp. Mar. Biol. Ecol., 281: 109-121. doi:10.1016/S0022-0981(02)00441-0
Boaventura, D., L.C. Fonseca and C. Teles-Ferreira. – 1999. Trophic structure of macrobenthic communities on the Portuguese coast. A review of lagonal, estuarine and rocky littoral habitats. Acta Oecol., 20(4): 407-415. doi:10.1016/S1146-609X(99)00127-7
Cardoso, P.G., M.A. Pardal, A.I. Lillebø, S.M. Ferreira, D. Raffaelli and J.C. Marques. – 2004. Dynamic changes in seagrass assemblages under eutrophication and implications for recovery. J. Exp. Mar. Biol. Ecol., 302: 233-248. doi:10.1016/j.jembe.2003.10.014
Chícharo, L., J. Regala, M. Gaspar, F. Alves and M.A. Chícharo. – 2002a. Macrofauna spatial differences within clam dredgetracks and their implications for short-term fishing effects studies. Fish. Res., 54: 349-353. doi:10.1016/S0165-7836(01)00272-7
Chícharo, L., M.A. Chícharo, M.Gaspar, J. Regala and F. Alves. – 2002b. Reburial time and indirect mortality of Spisula solida clams caused by dredging. Fish. Res., 59: 247-257. doi:10.1016/S0165-7836(02)00012-7
Chícharo, M.A., L. Chícharo, A. Amaral, S. Condinho and M. Gaspar. – 2003. Chronic effects of dredging-induced stress on the clam (Spisula solida): nucleic acid and lipid composition. Fish. Res., 63: 447-452 doi:10.1016/S0165-7836(03)00077-8
Connor, D.W., H. Allen, N. Golding, K.L. Howell, L.M. Lieberknecht, K.O. Northen, and J.B. Reker. – 2004. The Marine Habitat Classification for Britain and Ireland Version 04.05 JNCC, Peterborough ISBN 1 861 07561 8 [internet version]. Available from www.jncc.gov.uk/MarineHabitatClassification [cited 22 February 2005].
Costa, M., R. Silva and J. Vitorino. – 2001. Contribuição para o estudo do clima de agitação marítima na costa portuguesa. 2as Jornadas de Engenharia Costeira e Portuária, (CD-ROM). Laboratório Nacional de Engenharia Civil, Lisbon.
Desroy, N., C. Warembourg, J.M. Dewarumez and J.C. Dauvin. – 2002. Macrobenthic resources of the shallow soft-bottom sediments in the eastern English Channel and southern North Sea. ICES J. Mar. Sci., 60: 120–131. doi:10.1006/jmsc.2002.1333
Dolbeth, M., I. Viegas, F. Martinho, J.C. Marques and M.A. Pardal. – 2006. Population structure and species dynamics of Spisula solida, Diogenes pugilator and Branchiostoma lanceolatum along a temporal-spatial gradient in the south coast of Portugal. Estuar. Coast. Shelf Sci., 66: 168-176. doi:10.1016/j.ecss.2005.08.006
Dolbeth, M., Ó. Ferreira, H. Teixeira, J.C. Marques, J.A. Dias and M.A. Pardal. – 2007. Beach morphodynamics impact on a macrobenthic community along a subtidal depth gradient. Mar. Ecol. Prog. Ser., 352: 113-124. doi:10.3354/meps07040
Fauchald, K. and P.A. Jumars. – 1979. The diet of worms: a study of polychaete feeding guilds. Oceanogr. Mar. Biol. Ann. Rev., 17: 193-284.
Ferreira, Ó., J.C. Martins and J.A. Dias. – 1997. Morfodinâmica e vulnerabilidade da Praia de Faro, pp. 67-76. Seminário sobre a Zona Costeira do Algarve, Faro.
Gaspar, M.B., R. Ferreira and C.C. Monteiro. – 1999a. Growth and reproductive cycle of Donax trunculus L., (Mollusca: Bivalvia) off Faro, southern Portugal. Fish. Res., 41: 309-316. doi:10.1016/S0165-7836(99)00017-X
Gaspar, M.B., M. Castro and C.C. Monteiro. – 1999b. Effect of tooth spacing and mesh size on the catch of the Portuguese clam and razor clam dredge. ICES J. Mar. Sci., 56: 103-110. doi:10.1006/jmsc.1998.0423
Gaspar, M.B., L. Leitão, M.N. Santos, M. Sobral, L. Chícharo, A. Chícharo and C.C. Monteiro. – 2002. Influence of mesh size and tooth spacing on the proportion of damaged organisms in the catches of the Portuguese clam dredge fishery. ICES J. Mar. Sci., 59: 1228-1236. doi:10.1006/jmsc.2002.1310
Gaston, G.R. – 1987. Benthic Polychaeta of the Middle Atlantic Bight: feeding and distribution. Mar. Ecol. Prog. Ser., 36: 251-262. doi:10.3354/meps036251
Gaudêncio, M.J. and H.N. Cabral. – 2007. Trophic structure of macrobenthos in the Tagus estuary and adjacent coastal shelf. Hydrobiologia, 587: 241-251. doi:10.1007/s10750-007-0686-6
Gili, J.M. and R. Coma. – 1998. Benthic suspension feeders: their paramount role in littoral marine food webs. Trends Ecol. Evol., 13: 316-321. doi:10.1016/S0169-5347(98)01365-2
Hewitt, J.E., V.J. Cummings, J.I. Ellisa, G. Funnella, A. Norkko, T.S. Talley and S.F. Thrush. – 2003. The role of waves in the colonisation of terrestrial sediments deposited in the marine environment. J. Exp. Mar. Biol. Ecol., 290: 19-47. doi:10.1016/S0022-0981(03)00051-0
Hoey, V.G., S. Degraer and M. Vincx. – 2004. Macronbenthic community structure of the soft bottom sediments at the Belgian Continental Shelf. Estuar. Coast. Shelf Sci., 59: 599-613. doi:10.1016/j.ecss.2003.11.005
Incera, M., S.P. Cividanes, J. López and R. Costas. – 2003. Role of hydrodynamic conditions on quantity and biochemical composition of sediment organic matter in sandy intertidal sediments (NW Atlantic coast, Iberian Peninsula). Hydrobiologia, 497: 39-51. doi:10.1023/A:1025405519829
Laudien, J., M. Herrmann and W.E. Arntz. – 2007. Soft bottom species richness and diversity as a function of depth and iceberg scour in Arctic glacial Kongsfjorden (Svalbard). Polar Biol., 30: 1035-1046. doi:10.1007/s00300-007-0263-5
Levin, L.A. and C. DiBacco. – 1995. Influence of sediment transport on short-term recolonization by seamount infauna. Mar. Ecol. Prog. Ser., 123: 163-175. doi:10.3354/meps123163
Levinton, J. and B. Kelaher. – 2004. Opposing organizing forces of deposit-feeding marine communities. J. Exp. Mar. Biol. Ecol., 300: 65-82. doi:10.1016/j.jembe.2003.12.008
Limnologisk Metodik. – 1992. Ferskvandsbiologisk Laboratorium. Københavns Universitet (Ed.), Akademisk Forlag, København. Mancinelli, G., S. Fazi and L. Rossi. – 1998. Sediment structural properties mediating dominant feeding types patterns in softbottom macrobenthos of the Northern Adriatic Sea. Hydrobiologia, 367: 211-222.
MarLin – Marine Life Information Network: Biology and Sensitivity Key Information Sub-programme [on-line]. Plymouth: Marine Biological Association of the United Kingdom. http://www.marlin.ac.uk/sah/species_information.php.
Morin, J.G., J.E. Kastendiek, A. Harrington and N.N. Davis – 1985. Organization and patterns of interactions in a subtidal sand community on an exposed coast. Mar. Ecol. Prog. Ser., 27: 163-185 doi:10.3354/meps027163
Muniz, P. and A.M.S. Pires. – 1999. Trophic structure of the polychaetes in the São Sebastião Channel (southeastern Brazil). Mar. Biol., 134: 517-528. doi:10.1007/s002270050567
Nicholls, R.J., W.A. Birkemeier and G. Lee. – 1998. Evaluation of depth of closure using data from Duck, NC, USA. Mar. Geol., 148: 179-201. doi:10.1016/S0025-3227(98)00011-5
Oug, E., K. Næsm and B. Rygg. – 1998. Relationship between soft bottom Macrofauna and polycyclic aromatic hydrocarbons (PAH) from smelter discharge in Norwegian fjords and coastal waters. Mar. Ecol. Prog. Ser., 173: 39-52. doi:10.3354/meps173039
Parsons, T.R., Y. Maita and C.M. Lally. – 1985. Pigments. In: T.R. Parsons (ed.), A Manual of Chemical and Biological Methods for Seawater Analysis, pp. 101-104. Pergamon Press, Oxford.
Pinet, P.R. – 2003. Invitation to Oceanography (3rd ed.). Jones and Barlett publishers Canada, Mississauga.
Rosenberg, R. – 1995. Benthic marine fauna structured by hydrodynamic processes and food availability. Neth. J. Sea Res., 34: 303-317. doi:10.1016/0077-7579(95)90040-3
Roth, S. and J.G. Wilson. – 1998. Functional analysis by trophic guilds of macrobenthic community structure in Dublin Bay, Ireland. J. Exp. Mar. Biol. Ecol., 222: 195-217. doi:10.1016/S0022-0981(97)00145-7
San Vicente, C. and J.C. Sorbe. – 1999. Spatio-temporal structure of the suprabenthic community from the Creixell beach (western Mediterranean). Acta Oecol., 20(4): 377-389. doi:10.1016/S1146-609X(99)00129-0
Sardá, R., S. Pinedo and D. Martin. – 1999. Seasonal dynamics of macroinfaunal key species inhabiting shallow soft-bottoms in the Bay of Blanes (NW Mediterranean). Acta Oecol., 20(4): 315-326. doi:10.1016/S1146-609X(99)00135-6
Sardá, R., S. Pinedo, A. Grémare and S. Taboada. – 2000. Changes in the dynamics of shallow sandy-bottom assemblages due to sand extraction in the Catalan Western Mediterranean Sea. ICES J. Mar. Sci., 57: 1446-1453. doi:10.1006/jmsc.2000.0922
Shepard, F.P. – 1954. Nomenclature based on sand-silt-clay ratios. J. Sediment. Petrol., 24: 151-158.
Snelgrove, P.V.R. and C.A. Butman. – 1994. Animal-sediment relationships revisited – cause versus effect. Oceanog. Mar. Biol., 32: 111-117.
Sprung, M. – 1994. Macrobenthic secondary production in the intertidal zone of Ria Formosa-a lagoon in southern Portugal. Estuar. Coast. Shelf Sci., 38: 539-558. doi:10.1006/ecss.1994.1037
Strickland, J.D.M. and T.R. Parsons. – 1972. A Practical Handbook of Seawater Analysis (2nd ed.). Fisheries Research Board of Canada, Ottawa.
Tirelli, T., M. Dappiano, G. Maiorana and P. Pessani. – 2000. Intraspecific relationship of the hermit crab Diogenes pugilator: predation and competition. Hydrobiologia, 439: 43-48. doi:10.1023/A:1004197518769
Urban-Malinga, B. and J. Wiktor. – 2003. Microphytobenthic primary production along a non-tidal sandy beach gradient: an annual study from the Baltic Sea. Oceanologia, 45: 705-720.
Wieking, G. and I. Kröncke. – 2003. The Dogger Bank example Macrofauna communities of the Dogger Bank (central North Sea) in the late 1990s: spatial distribution, species composition and trophic structure. Helgol. Mar. Res., 57: 34-46.
Wieking, G. and I. Kröncke. – 2005. Is benthic trophic structure affected by food quality? The Dogger Bank example. Mar. Biol., 146: 387-400. doi:10.1007/s00227-004-1443-2
Wildish, D. and D. Kristmanson. – 1997. Benthic suspension feeders and flow. Cambridge University Press, USA.
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