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East-west spatial groupings in intertidal communities, environmental drivers and key species

Published online by Cambridge University Press:  25 October 2016

Julian Merder
Affiliation:
Institute for Chemistry and Biology of the Marine Environment, University of Oldenburg, Oldenburg, Niedersachsen, Germany
Jan A. Freund
Affiliation:
Institute for Chemistry and Biology of the Marine Environment, University of Oldenburg, Oldenburg, Niedersachsen, Germany
Lukas Meysick
Affiliation:
Institute for Chemistry and Biology of the Marine Environment, University of Oldenburg, Oldenburg, Niedersachsen, Germany
Christina Simkanin
Affiliation:
Smithsonian Environmental Research Center, Edgewater, Maryland, USA
Ruth M. O'Riordan
Affiliation:
School of Biological, Earth & Environmental Sciences, University College Cork, Distillery Fields, North Mall, Cork, Ireland
Anne Marie Power*
Affiliation:
Martin Ryan Institute, National University of Ireland Galway, Galway, Ireland
*
Correspondence should be addressed to:A.M. Power, Martin Ryan Institute, National University of Ireland Galway, Galway, Ireland email: [email protected]

Abstract

The rocky intertidal communities of Ireland contain a mix of cold- and warm-adapted species, however the spatial distribution of these communities has not been investigated in a systematic way. Based on a benthic community dataset collected in 2003 at 63 sites, several statistical analyses were combined with the aims of (i) detecting groups of similar communities and their spatial arrangement, (ii) relating these groups to environmental factors and (iii) identifying the species that drive the different community groups. Sørensen's index suggested two marine community groups, one of the east and south-east (termed ‘east’) and the other in the west, south-west and north (termed ‘west’). A second partition based on combined wave exposure and sea surface chlorophyll comprised four groups, as did a further partition based on combined sea surface and air temperatures. The spatial arrangement of wave height plus chlorophyll conditions agreed reasonably well with the binary marine community partition, but the temperature partition did not. The ‘east’ community appeared to be associated with low wave height and chlorophyll conditions. The species that were most influential to the ‘east’ community were Balanus crenatus, Austrominius modestus and Fucus vesiculosus. The ‘west’ sites were associated with high wave height/low chlorophyll (with some variation in this due to local shelter) and the species Paracentrotus lividus, Chthamalus stellatus, Alaria esculenta and Himanthalia elongata. A longitudinal pattern rather than one associated with latitude was evident in this marine community and local drivers rather than temperature clines appeared most important for the dominant community patterns.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2016 

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References

REFERENCES

Allen, B.M., Power, A.M., O'Riordan, R.M., Myers, A.A. and McGrath, D. (2006) Increases in the abundance of the invasive barnacle Elminius modestus Darwin in Ireland. Biology and Environment: Proceedings of the Royal Irish Academy 106B, 155161.Google Scholar
Andrews, H.L. (1945) The kelp beds of the Monterey region. Ecology 26, 2437.CrossRefGoogle Scholar
Ballantine, W.J. (1961) A biologically-defined exposure scale for the comparative description of rocky shores. Field Studies 1, 119.Google Scholar
Barry, J.P., Baxter, C.H., Sagarin, R.D. and Gilman, S.E. (1995) Climate-related, long-term faunal changes in a California rocky intertidal community. Science 267, 672675.Google Scholar
Borcard, D., Gillet, F. and Legendre, P. (2011) Numerical ecology with R. New York, NY: Springer, pp. 17.Google Scholar
Bruton, T., Lyons, H., Lerat, Y., Stanley, M. and Rasmussen, M.B. (2009) A Review of the Potential of Marine Algae as a Source of Biofuel in Ireland. Sustainable Energy Ireland Available at http://www.seai.ie/Publications/Renewables_Publications_/Bioenergy/Algaereport.pdf Google Scholar
Burrows, M.T. (2012) Influences of wave fetch, tidal flow and ocean colour on subtidal rocky communities. Marine Ecology Progress Series 445, 193207.Google Scholar
Burrows, M.T., Harvey, R. and Robb, L. (2008) Wave exposure indices from digital coastlines and the prediction of rocky shore community structure. Marine Ecology Progress Series 353, 112.Google Scholar
Chase, J.M., Kraft, N.J., Smith, K.G., Vellend, M. and Inouye, B.D. (2011) Using null models to disentangle variation in community dissimilarity from variation in α-diversity. Ecosphere 2, 111.CrossRefGoogle Scholar
Clarke, K.R. and Warwick, R.M. (2001) Change in marine communities: An approach to statistical analysis and interpretation, 2nd edition. Plymouth: PRIMER-E.Google Scholar
Connell, J.H. (1985) The consequences of variation in initial settlement vs post-settlement mortality in rocky intertidal communities. Journal of Experimental Marine Biology and Ecology 93, 1146.Google Scholar
Costello, M.J., Emblow, C.S. and Picton, B.E. (1996) Long term trends in the discovery of marine species new to science which occur in Britain and Ireland. Journal of the Marine Biological Association of the United Kingdom 76, 255257.CrossRefGoogle Scholar
Crisp, D.J. and Southward, A.J. (1958) The distribution of intertidal organisms along the coasts of the English Channel. Journal of the Marine Biological Association of the United Kingdom 37, 157203.Google Scholar
Cummins, V., Coughlan, S., McClean, O., Connolly, N., Mercer, J. and Burnell, G. (2002) An assessment of the potential for the sustainable development of the edible periwinkle, Littorina littorea, industry in Ireland. Marine Resource Series 22, 65 pp.Google Scholar
Delany, J., Myers, A.A., McGrath, D., O'Riordan, R.M. and Power, A.M. (2003) Role of post-settlement mortality and ‘supply-side’ ecology in setting patterns of intertidal distribution in the chthamalid barnacles Chthamalus montagui and C. stellatus . Marine Ecology Progress Series 249, 207214.CrossRefGoogle Scholar
Deutsch, C., Ferrel, A., Seibel, B., Pörtner, H.O. and Huey, R.B. (2015) Climate change tightens a metabolic constraint on marine habitats. Science 348, 11321135.Google Scholar
Dufrêne, M. and Legendre, P. (1997) Species assemblages and indicator species: the need for a flexible asymmetrical approach. Ecological Monographs 67, 345366.Google Scholar
Fahy, E., Healy, E., Downes, S., Alcorn, T. and Nixon, E. (2008) An atlas of fishing and some related activities in Ireland's territorial sea and internal marine waters with observations concerning their spatial planning. Irish Fisheries Investigations Series 19, 33 pp.Google Scholar
Firth, L.B. and Crowe, T.P. (2008) Large-scale coexistence and small-scale segregation of key species on rocky shores. Hydrobiologia 614, 233241.Google Scholar
Firth, L.B. and Williams, G.A. (2009) The influence of multiple environmental stressors on the limpet Cellana toreuma during the summer monsoon season in Hong Kong. Journal of Experimental marine Biology and Ecology 375, 7075.Google Scholar
Forbes, E. (1858) The distribution of marine life, illustrated chiefly by fishes, and molluscs and radiata. Edinburgh: A.K. Johnston's Physical Atlas. W. & A.J. Johnston, pp. 99101.Google Scholar
Gaines, S., Brown, S. and Roughgarden, J. (1985) Spatial variation in larval concentrations as a cause of spatial variation in settlement for the barnacle, Balanus glandula . Oecologia 67, 267272.Google Scholar
Grall, J. and Chauvaud, L. (2002) Marine eutrophication and benthos: the need for new approaches and concepts. Global Change Biology 8, 813830.CrossRefGoogle Scholar
Hawkins, S.J. (1981) The influence of season and barnacles on the algal colonization of Patella vulgata exclusion areas. Journal of the Marine Biological Association of the United Kingdom 61, 115.Google Scholar
Hawkins, S.J., Moore, P.J., Burrows, M.T., Poloczanska, E., Mieszkowska, N., Herbert, R.J.H., Jenkins, S.R., Thompson, R.C., Genner, M.J. and Southward, A.J. (2008) Complex interactions in a rapidly changing world: responses of rocky shore communities to recent climate change. Climate Research 37, 123133.Google Scholar
Helmuth, B., Harley, C.D., Halpin, P.M., O'Donnell, M., Hofmann, G.E. and Blanchette, C.A. (2002) Climate change and latitudinal patterns of intertidal thermal stress. Science 298, 10151017.Google Scholar
Hiscock, K., Southward, A., Tittley, I. and Hawkins, S. (2004) Effects of changing temperature on benthic marine life in Britain and Ireland. Aquatic Conservation: Marine Freshwater Ecosystems 14, 333362.Google Scholar
Ingólfsson, A. (2005) Community structure and zonation patterns of rocky shores at high latitudes: an interocean comparison. Journal of Biogeography 32, 169182.CrossRefGoogle Scholar
Jenkins, S.R., Norton, T.A. and Hawkins, S.J. (2004) Long term effects of Ascophyllum nodosum canopy removal on mid shore community structure. Journal of the Marine Biological Association of the United Kingdom 84, 327329.CrossRefGoogle Scholar
Kraufvelin, P., Christie, H. and Olsen, M. (2002) Littoral macrofauna (secondary) responses to experimental nutrient addition to rocky shore mesocosms and a coastal lagoon. Hydrobiologia 484, 149166.Google Scholar
Laffoley, D., Baxter, J., O'Sullivan, G., Greenaway, B., Colley, M., Naylor, L. and Hamer, J. (2005) The MarClim Project: Key messages for decision makers and policy advisors, and recommendations for future administrative arrangements and management measures. English Nature Research Reports No. 671.Google Scholar
Lewis, J.R. (1964) The ecology of rocky shores. London: English Universities Press.Google Scholar
Lewis, J.R. (1996) Coastal benthos and global warming: strategies and problems. Marine Pollution Bulletin 32, 698700.Google Scholar
McGinty, N., Johnson, M.P. and Power, A.M. (2014) Spatial mismatch between phytoplankton and zooplankton biomass at the Celtic Boundary Front. Journal of Plankton Research 36, 14461460.CrossRefGoogle Scholar
McQuaid, C.D. and Branch, G.M. (1984) Influence of sea temperature, substratum and wave exposure on rocky intertidal communities: an analysis of fauna and floral biomass. Marine Ecology Progress Series 19, 145151.Google Scholar
Moore, P.G. (1971) The nematode fauna associated with holdfasts of kelp (Laminaria hyperborea) in North-East Britain. Journal of the Marine Biological Association of the United Kingdom 51, 589604.CrossRefGoogle Scholar
Moore, P.G. (1973) The larger Crustacea associated with holdfasts of kelp (Laminaria hyperborea) in North-East Britain. Cahiers de Biologie Marine 14, 493518.Google Scholar
Neilson, B. and Costello, M.J. (1999) The relative lengths of seashore substrata around the coastline of Ireland as determined by digital methods in a geographical information system. Estuarine, Coastal and Shelf Science 49, 501508.Google Scholar
Pitt, N.R., Poloczanska, E.S. and Hobday, A.J. (2010) Climate-driven range changes in Tasmanian intertidal fauna. Marine and Freshwater Research 61, 963970.Google Scholar
Pizzolla, P.F. (2007) Paracentrotus lividus Purple sea urchin. In Tyler-Walters, H. and Hiscock, K. (eds) Marine life information network: biology and sensitivity key information reviews, [on-line]. Plymouth: Marine Biological Association of the United Kingdom. Available at http://www.marlin.ac.uk/species/detail/1499.Google Scholar
Poloczanska, E.S., Brown, C.J., Sydeman, W.J., Kiessling, W., Schoeman, D.S., Moore, P.J., Brander, K., Bruno, J.F., Buckley, L.B., Burrows, M.T., Duarte, C.M., Halpern, B.S., Holding, J., Kappel, C.V., O'Connor, M.I., Pandolfi, J.M., Parmesan, C., Schwing, F., Thompson, S.A. and Richardson, A.J. (2013) Global imprint of climate change on marine life. Nature Climate Change 3, 919925.CrossRefGoogle Scholar
Pörtner, H.O. (2001) Climate change and temperature-dependent biogeography: oxygen limitation of thermal tolerance in animals. Naturwissenschaften 88, 137146.Google Scholar
Pörtner, H.O. (2010) Oxygen- and capacity-limitation of thermal tolerance: a matrix for integrating climate-related stressor effects in marine ecosystems. Journal of Experimental Biology 213, 881893.Google Scholar
Power, A.M., Delany, J., Myers, A.A., O'Riordan, R.M. and McGrath, D. (1999) Prolonged settlement and prediction of recruitment in two sympatric intertidal Chthamalus species from south-west Ireland. Journal of the Marine Biological Association of the United Kingdom 79, 941943.CrossRefGoogle Scholar
Power, A.M., Delany, J., McGrath, D., Myers, A.A. and O'Riordan, R.M. (2006) Patterns of adult abundance in Chthamalus stellatus (Poli) and C. montagui Southward (Crustacea: Cirripedia) emerge during late recruitment. Journal of Experimental Marine Biology and Ecology 332, 151165.CrossRefGoogle Scholar
Power, A.M., McCrann, K., McGrath, D., O'Riordan, R.M., Simkanin, C. and Myers, A.A. (2011) Physiological tolerance predicts species composition at different scales in a barnacle guild. Marine Biology 158, 21492160.Google Scholar
Power, A.M., Myers, A.A., O'Riordan, R.M., McGrath, D. and Delany, J. (2001) An investigation into rock surface wetness as a parameter contributing to the distribution of the intertidal barnacles Chthamalus stellatus and C. montagui . Estuarine, Coastal and Shelf Science 52, 349356.CrossRefGoogle Scholar
Rattray, A., Ierodiaconou, D. and Womersley, T. (2015) Wave exposure as a predictor of benthic habitat distribution on high energy temperate reefs. Frontiers in Marine Science 2, 114.Google Scholar
R Development Core Team (2008) R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing. ISBN 3-900051-07-0, Available at http://www.R-project.org. Google Scholar
Simkanin, C., Power, A.M., Myers, A., McGrath, D., Southward, A., Mieszkowska, N., Leaper, R. and O'Riordan, R. (2005) Using historical data to detect temporal changes in the abundances of intertidal species on Irish shores. Journal of the Marine Biological Association of the United Kingdom 85, 13291340.CrossRefGoogle Scholar
Singh, A., Nigam, P.S. and Murphy, J.D. (2011) Mechanism and challenges in commercialisation of algal biofuels. Bioresource technology 102, 2634.Google Scholar
Southward, A.J. (1958) Note on the temperature tolerances of some intertidal animals in relation to environmental temperatures and geographical distribution. Journal of the Marine Biological Association of the United Kingdom 37, 4966.Google Scholar
Southward, A.J. (1991) Forty years of changes in species composition and population density of barnacles on a rocky shore near Plymouth. Journal of the Marine Biological Association of the United Kingdom 71, 495513.CrossRefGoogle Scholar
Southward, A.J. and Crisp, D.J. (1954) The distribution of certain intertidal animals around the Irish coast. Proceedings of the Royal Irish Academy B 57, 129.Google Scholar
Stephenson, T.A. and Stephenson, A. (1949) The universal features of zonation between tide-marks on rocky coasts. Journal of Ecology 37, 289305.Google Scholar
Sunday, J.M., Bates, A.E. and Dulvy, N.K. (2012) Thermal tolerance and the global redistribution of animals. Nature Climate Change 2, 686690.CrossRefGoogle Scholar
Sweeney, J. (2014) Regional weather and climates of the British Isles – Part 6: Ireland. Weather 69, 2027.CrossRefGoogle Scholar
Valdivia, N., Aguilera, M.A., Navarrete, S.A. and Broitman, B.R. (2015) Disentangling the effects of propagule supply and environmental filtering on the spatial structure of a rocky shore metacommunity. Marine Ecology Progress Series 538, 6779.Google Scholar
Werner, A. and Kraan, S. (2004) Review of the potential mechanisation of kelp harvesting in Ireland. Marine Environment and Health Series 17, 152, Marine Institute, Galway.Google Scholar
Wieters, E.A., Broitman, B.R. and Branch, G.M. (2009) Benthic community structure and spatiotemporal thermal regimes in two upwelling ecosystems: comparisons between South Africa and Chile. Limnology and Oceanography 54, 10601072.Google Scholar
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