Abstract
Physical disturbance is a key factor in controlling the spatial and temporal composition of shallow-water benthic communities. Like shallow waters, deeper waters are increasingly subject to a range of anthropogenic disturbances, which can lead to significant alterations in sedimentation patterns. These alterations often exceed naturally occurring changes. We used a combined analysis of six independent data sets arising from large-scale field surveys and small-scale laboratory experiments to investigate the effects of seabed disturbance on nematode communities. Disturbance response was documented as a function of disturbance type (coastal development, dredged material disposal, bottom trawling, glacial fjord) and intensity (low, medium, high). Natural and man-induced seabed disturbance exerted differential effects on exposed populations, generating changes in the taxonomic (genus) and functional (feeding type) attributes of their assemblages. The genus composition of nematode assemblages from geographically separate seas converged with increased level of various types of man-made disturbance. Assemblages present along a gradient of natural disturbance in a glacial fjord followed an opposite response vector, suggesting that community changes induced by anthropogenic activities, or experimental treatments simulating the principal impacts of these, inherently differ from disturbance of natural origin. Changes in trophic diversity and structure were primarily driven by factors confounded with physical disturbance, such as metal contamination. Coupling the results of analyses at multiple scales proved a useful means of providing deeper insights into the general response of ecological communities to environmental change.
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References
Alongi DM (1985) Effects of physical disturbance on population dynamics and trophic interactions among microbes and meiofauna. J Mar Res 43:351–364
Anderson MJ, Willis TJ (2003) Canonical analysis of principal coordinates: a useful method of constrained ordination for ecology. Ecology 84:511–525. doi:https://doi.org/10.1890/0012-9658(2003)084[0511:CAOPCA]2.0.CO;2
Armonies W (1994) Drifting meio- and macrobenthic invertebrates on tidal flats in Königshafen: a review. Helgol Wiss Meeresunters 48:299–320. doi:https://doi.org/10.1007/BF02367043
Boyd SE, Rees HL, Richardson CA (2000) Nematodes as sensitive indicators of change at dredged material disposal sites. Estuar Coast Shelf Sci 51:805–819. doi:https://doi.org/10.1006/ecss.2000.0722
Chandrasekara WU, Frid CLJ (1998) A laboratory assessment of the survival and vertical movement of two epibenthic gastropod species, Hydrobia ulvae (Pennant) and Littorina littorea (Linnaeus), after burial in sediment. J Exp Mar Biol Ecol 221:191–207. doi:https://doi.org/10.1016/S0022-0981(97)00123-8
Clarke KR (1993) Non-parametric multivariate analyses of changes in community structure. Aust J Ecol 18:117–143. doi:https://doi.org/10.1111/j.1442-9993.1993.tb00438.x
Clarke KR, Ainsworth M (1993) A method of linking multivariate community structure to environmental variables. Mar Ecol Prog Ser 92:205–219. doi:https://doi.org/10.3354/meps092205
Clarke KR, Gorley RN (2006) PRIMER v6. user manual. Primer-E Ltd, Plymouth
Clarke KR, Warwick RM (1998a) A taxonomic distinctness index and its statistical properties. J Appl Ecol 35:523–531. doi:https://doi.org/10.1046/j.1365-2664.1998.3540523.x
Clarke KR, Warwick RM (1998b) Quantifying structural redundancy in ecological communities. Oecologia 113:278–289. doi:https://doi.org/10.1007/s004420050379
Clarke KR, Warwick RM (2001a) A further biodiversity index applicable to species lists: variation in taxonomic distinctness. Mar Ecol Prog Ser 216:265–278. doi:https://doi.org/10.3354/meps216265
Clarke KR, Warwick RM (2001b) Change in marine communities: an approach to statistical analysis and interpretation, 2nd edn. Primer-E Ltd, Plymouth
Clarke KR, Somerfield PJ, Chapman MG (2006) On resemblance measures for ecological studies, including taxonomic dissimilarities and zero-adjusted Bray–Curtis coefficient for denuded assemblages. J Exp Mar Biol Ecol 330:55–80. doi:https://doi.org/10.1016/j.jembe.2005.12.017
Clarke KR, Somerfield PJ, Gorley RN (2008) Testing of null hypotheses in exploratory community analyses: similarity profiles and biota-environment linkage. J Exp Mar Biol Ecol 366:56–69. doi:https://doi.org/10.1016/j.jembe.2008.07.009
Collie JS, Hall SJ, Kaiser MJ, Poiner IR (2000) A quantitative analysis of fishing impacts on shelf-sea benthos. J Anim Ecol 69:785–789. doi:https://doi.org/10.1046/j.1365-2656.2000.00434.x
Commito JA, Tita G (2002) Differential dispersal rates in an intertidal meiofauna assemblage. J Exp Mar Biol Ecol 268:237–256. doi:https://doi.org/10.1016/S0022-0981(01)00386-0
Connell JH (1978) Diversity in tropical rain forests and coral reefs. Science 199:1302–1310. doi:https://doi.org/10.1126/science.199.4335.1302
Coull BC, Chandler GT (1992) Pollution and meiofauna: field, laboratory and mesocosm studies. Oceanogr Mar Biol Annu Rev 30:191–271
Death RG, Winterbourn MJ (1995) Diversity patterns in stream benthic invertebrate communities: the influence of habitat stability. Ecology 76:1446–1460. doi:https://doi.org/10.2307/1938147
Dernie KM, Kaiser MJ, Warwick RM (2003) Recovery rates of benthic communities following physical disturbance. J Anim Ecol 72:1043–1056. doi:https://doi.org/10.1046/j.1365-2656.2003.00775.x
Draggan S, Reisa JJ (1980) Controlling toxic substances: historical perspective and future research needs. In: Giesy JP (ed) Microcosms in ecological research. Technical Information Centre, US Department of Energy, Springfield, p 45
Ellis J, Cummings V, Hewitt J, Thrush S, Norkko A (2002) Determining effects of suspended sediment on condition of a suspension feeding bivalve (Atrina zelandica): results of a survey, a laboratory experiment and a field transplant experiment. J Exp Mar Biol Ecol 267:147–174. doi:https://doi.org/10.1016/S0022-0981(01)00355-0
Fegley SR (1988) Experimental variation of near-bottom current speeds and its effect on depth distribution of sand-living meiofauna. Mar Biol (Berl) 95:183–191. doi:https://doi.org/10.1007/BF00409004
Fernandez-Duque E, Veleggia C (1993) Meta-analysis: a valuable tool in conservation research. Conserv Biol 8:555–561. doi:https://doi.org/10.1046/j.1523-1739.1994.08020555.x
Gaston GR, Rakocinski CF, Brown SS, Cleveland CM (1998) Trophic function in estuaries: response of macrobenthos to natural and contaminant gradients. Mar Freshw Res 49:833–846. doi:https://doi.org/10.1071/MF97089
Giesy JP, Odum EP (1980) Microcosmology: introductory comments. In: Giesy JP (ed) Microcosms in ecological research. Technical Information Centre, US Department of Energy, Springfield, pp 1–13
Hagerman GM, Rieger RM (1981) Dispersal of benthic meiofauna by wave and current action in Bogue Sound, North Carolina, USA. Mar Ecol (Berl) 2:245–270. doi:https://doi.org/10.1111/j.1439-0485.1981.tb00099.x
Hall SJ (1994) Physical disturbance and marine benthic communities: life in unconsolidated sediments. Oceanogr Mar Biol Annu Rev 32:179–239
Heip C, Vincx M, Vranken G (1985) The ecology of marine nematodes. Oceanogr Mar Biol Annu Rev 23:399–489
Heip C, Huys R, Vincx M, Vanreusel A, Smol N, Herman R, Herman PMJ (1990) Composition, distribution, biomass and production of North Sea meiofauna. Neth J Sea Res 26:333–342. doi:https://doi.org/10.1016/0077-7579(90)90095-X
Hill MO (1973) Diversity and evenness: a unifying notation and its consequences. Ecology 54:427–432. doi:https://doi.org/10.2307/1934352
Huston MA (1994) Biological diversity. Cambridge University Press, Cambridge
Jayasree K, Warwick RM (1977) Free-living marine nematodes of a polluted sandy beach in the Firth of Clyde, Scotland: description of seven new species. J Nat Hist 11:289–302. doi:https://doi.org/10.1080/00222937700770211
Jennings S, Kaiser MJ (1998) The effects of fishing on marine ecosystems. Adv Mar Biol 34:201–352. doi:https://doi.org/10.1016/S0065-2881(08)60212-6
Jensen P (1984) Ecology of benthic and epiphytic nematodes in brackish water. Hydrobiologia 108:201–217
Karakassis I, Papadopoulou KN, Dafnomili EN, Plaiti W, Wilkinson M (1993) Preliminary study of the environmental contitions of Iraklion harbour. Proceedings of the 4th national symposium in oceanography and fisheries, Rhodes, Greece, pp 397–400
Kern JC (1990) Active and passive aspects of meiobenthic copepod dispersal at two sites near Mustang Island, Texas. Mar Ecol Prog Ser 60:211–223. doi:https://doi.org/10.3354/meps060211
Lampadariou N, Austen MC, Robertson N, Vlachonis G (1997) Analysis of meiobenthic community structure in relation to pollution and disturbance in Iraklion harbour, Greece. Vie Milieu 47:9–24
Lee HJ, Vanhove S, Peck LS, Vincx M (2001) Recolonisation of meiofauna after catastrophic iceberg scouring in shallow Antarctic sediments. Polar Biol 24:918–925. doi:https://doi.org/10.1007/s003000100300
Leffler JW (1980) Microcosmology: theoretical applications of biological models. In: Giesy JP (ed) Microcosms in ecological research. Technical Information Centre, US Department of Energy, Springfield, pp 14–29
Lopez-Jamar E, Mejuto J (1988) Infaunal benthic recolonisation after dredging operations in La Coruna Bay, NW Spain. Cah Biol Mar 29:37–49
Mackey RL, Currie DJ (2001) The diversity–disturbance relationship: is it generally strong and peaked? Ecology 82:3479–3492
Maurer D, Keck RT, Tinsman JC, Leathem WA, Wethe C, Lord C, Church TM (1986) Vertical migration and mortality of marine benthos in dredged material: a synthesis. Int Rev Ges Hydrobiol 71:49–63
McCarthy JM, Hein CL, Olden JD, vander Zanden MJ (2006) Coupling long-term studies with meta-analysis to investigate impacts of non-native crayfish on zoobenthic communities. Freshw Biol 51:224–235. doi:https://doi.org/10.1111/j.1365-2427.2005.01485.x
Medina MH, Correa JA, Barata C (2007) Micro-evolution due to pollution: possible consequences for ecosystem responses to toxic stress. Chemosphere 67:2105–2114. doi:https://doi.org/10.1016/j.chemosphere.2006.12.024
Modig H, Ólafsson E (1998) Responses of Baltic benthic invertebrates to hypoxic events. J Exp Mar Biol Ecol 229:133–148. doi:https://doi.org/10.1016/S0022-0981(98)00043-4
Moore CG, Bett BJ (1989) The use of meiofauna in marine pollution impact assessment. Zool J Linn Soc 96:263–280. doi:https://doi.org/10.1111/j.1096-3642.1989.tb01831.x
Nichols FH, Thompson JK (1985) Persistence of an introduced mudflat community in South Francisco Bay, California. Mar Ecol Prog Ser 24:83–97. doi:https://doi.org/10.3354/meps024083
Palen WJ, Williamson CE, Clauser AA, Schindler DE (2005) Impact of UV-B exposure on amphibian embryos: linking species physiology and oviposition behaviour. Proc R Soc Lond B Biol Sci 272:1227–1234. doi:https://doi.org/10.1098/rspb.2005.3058
Quinn G, Keough M (2002) Experimental design and data analysis for biologists. Cambridge University Press, Cambridge
Rakocinski CF, Brown SS, Gaston GR, Heard RW, Walker WW, Summers JK (1997) Macrobenthic responses to natural and contaminant-related gradients in northern Gulf of Mexico estuaries. Ecol Appl 7:1278–1298. doi:https://doi.org/10.1890/1051-0761(1997)007[1278:MRTNAC]2.0.CO;2
Rome MS, Young-Williams AC, Davis GR, Hines AH (2005) Linking temperature and salinity tolerance to winter mortality of Chesapeake Bay blue crabs (Callinectes sapidus). J Exp Mar Biol Ecol 319:129–145. doi:https://doi.org/10.1016/j.jembe.2004.06.014
Schratzberger M, Jennings S (2002) Impacts of chronic trawling disturbance on meiofaunal communities. Mar Biol (Berl) 141:991–1000. doi:https://doi.org/10.1007/s00227-002-0895-5
Schratzberger M, Warwick RM (1998) Effects of physical disturbance on nematode communities in sand and mud: a microcosm experiment. Mar Biol (Berl) 130:643–650. doi:https://doi.org/10.1007/s002270050286
Schratzberger M, Rees HL, Boyd SE (2000) Effects of simulated deposition of dredged material on structure of nematode assemblages: the role of contamination. Mar Biol (Berl) 137:613–622. doi:https://doi.org/10.1007/s002270000386
Schratzberger M, Maxwell TAD, Warr K, Rogers SI (2008) Spatial variability of infaunal nematode and polychaete assemblages in two muddy subtidal habitats. Mar Biol (Berl) 153:621–642. doi:https://doi.org/10.1007/s00227-007-0836-4
Somerfield PJ, Clarke KR (1995) Taxonomic levels, in marine community studies, revisited. Mar Ecol Prog Ser 127:113–119. doi:https://doi.org/10.3354/meps127113
Somerfield PJ, Warwick RM (1996) Meiofauna in marine pollution monitoring programmes: a laboratory manual. Ministry of AgricultureFisheries and Food, Directorate of Fisheries Research, Lowestoft
Somerfield PJ, Rees HL, Warwick RM (1995) Interrelationships in community structure between shallow-water marine meiofauna and macrofauna in relation to dredging disposal. Mar Ecol Prog Ser 127:103–112. doi:https://doi.org/10.3354/meps127103
Somerfield PJ, Warwick RM, Moens T (2005) Chapter 6: Meiofauna techniques. In: Eleftheriou A, McIntyre A (eds) Methods for the study of marine benthos, 3rd edn. Blackwell Science Ltd, Oxford, pp 229–272
Somerfield PJ, Cochrane SJ, Dahle S, Pearson TH (2006) Free-living nematodes and macrobenthos in a high-latitude glacial fjord. J Exp Mar Biol Ecol 330:284–296. doi:https://doi.org/10.1016/j.jembe.2005.12.034
Sousa WP (1979) Disturbance in marine intertidal boulder fields: the non-equilibrium maintenance of species diversity. Ecology 60:1225–1239. doi:https://doi.org/10.2307/1936969
Sousa WP (1984) The role of disturbance in natural communities. Annu Rev Ecol Syst 15:353–391. doi:https://doi.org/10.1146/annurev.es.15.110184.002033
Thistle D (1981) Natural physical disturbances and communities of marine soft bottoms. Mar Ecol Prog Ser 6:223–228. doi:https://doi.org/10.3354/meps006223
Tietjen JH (1980) Population structure and species composition of the free-living nematodes inhabiting sands of the New York Bight Apex. Estuar Coast Mar Sci 10:61–73. doi:https://doi.org/10.1016/S0302-3524(80)80049-1
Ullberg J, Ólafsson E (2003) Effects of biological disturbance by Monoporeia affinis (Amphipoda) on small-scale migration of marine nematodes in low-energy soft sediments. Mar Biol (Berl) 143:867–874. doi:https://doi.org/10.1007/s00227-003-1139-z
Vandepitte L, Vanaverbeke J, Vanhoorne B, Hernandez F, Campinas-Bezerra T, Mees J, Vanden Berghe E (2008) The MANUELA database: an integrated database on meiobenthos from European marine waters. Meiofauna Marina (submitted)
Vincx M (1990) Diversity of the nematode communities in the Southern Bight of the North Sea. Neth J Sea Res 25:181–188. doi:https://doi.org/10.1016/0077-7579(90)90019-D
Warwick RM (1993) Environmental impact studies on marine communities: pragmatical considerations. Aust J Ecol 18:63–80. doi:https://doi.org/10.1111/j.1442-9993.1993.tb00435.x
Warwick RM, Clarke KR (1998) Taxonomic distinctness and environmental assessment. J Appl Ecol 35:532–543. doi:https://doi.org/10.1046/j.1365-2664.1998.3540532.x
Warwick RM, Clarke KR (2001) Practical measures of marine biodiversity based on relatedness of species. Oceanogr Mar Biol Annu Rev 39:207–231
Warwick RM, Platt HM, Clarke KR, Agard J, Gobin J (1990) Analysis of macrobenthic and meiobenthic community structure in relation to pollution and disturbance in Hamilton Harbour, Bermuda. J Exp Mar Biol Ecol 138:119–142. doi:https://doi.org/10.1016/0022-0981(90)90180-K
Wieser W (1953) Die Beziehung zwischen Mundhöhlengestalt, Ernährungsweise und Vorkommen bei freilebenden marinen Nematoden. Ark Zool 4:439–484
Wlodarsaka-Kowalczuk M, Pearson TH, Kendall MA (2005) Benthic response to chronic natural physical disturbance by glacial sedimentation in an Arctic fjord. Mar Ecol Prog Ser 303:31–34. doi:https://doi.org/10.3354/meps303031
Acknowledgments
This work is a contribution to the responsive mode project Manuela (Meiobenthic and nematode biodiversity: unravelling ecological and latitudinal aspects) within the EU FP6 Network of Excellence MarBEF (contract no. GOCE-CT-2003-505446). MS received financial support from Defra (project ME4118, Environmental indicators: a structured approach to the evaluation of impacts arising from human activities at sea). PJS acknowledges financial support from the UK NERC and Defra (project ME3109, Assessment of marine biodiversity linked to ecosystems).
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Schratzberger, M., Lampadariou, N., Somerfield, P.J. et al. The impact of seabed disturbance on nematode communities: linking field and laboratory observations. Mar Biol 156, 709–724 (2009). https://doi.org/10.1007/s00227-008-1122-9
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DOI: https://doi.org/10.1007/s00227-008-1122-9