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Effects of topography on the environment

Published online by Cambridge University Press:  19 January 2010

A.C. Jackson
A.C. Jackson*
Affiliation:
Centre for Research on Ecological Impacts of Coastal Cities, Marine Laboratories A11, School of Biological Sciences, The University of Sydney, NSW 2006, Australia
*
Correspondence should be addressed to: A.C. Jackson, Environmental Research Centre, North Highland College UHI Millennium Institute, Castle Street, Thurso, Caithness, KW14 7JD, UK email: [email protected]
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Abstract

Greater understanding of patterns of distributions of organisms and their causal mechanisms are required if the consequences of climatic change are to be fully realized. Associations between topographic features of the environment and distributions of organisms are frequently assumed to be a consequence of provision or modification of local conditions by those features. Such assumptions are rarely supported empirically and there is increasing evidence that topographic features do not always influence variables in the way we might anticipate. Thus, data about how features of habitat influence environmental conditions, including availability of food, are likely to be useful for understanding how and why organisms are found where they are. Such data are few and rigorous descriptions about what defines particular features of habitat are seldom provided or are simplistic. For hard substrata in aquatic environments, crevices are often prominent features with which many species associate. Crevices have frequently been assumed, but not demonstrated, to ameliorate conditions by increasing humidity, moderating (usually reducing) temperatures and by decreasing forces from wave-impacts and water-flow. This study provided clear definitions and tests of various hypotheses about how crevices altered the local environment. The main predictions were that crevices would be cooler, more humid, more sheltered from water-movement and support more micro-algae than areas away from crevices. Manipulative experiments using artificial habitats and measurements on natural rocky shores were carried out on multiple shores over two years to understand how crevices affected local conditions. Crevices were indeed cooler, more humid, supported more micro-algae and more sheltered from water-flow than open areas nearby, but conditions did not always vary in ways that were expected. Effects were often complex, with factors such as season, height on the shore and tidal conditions interacting to influence how crevices affect environmental conditions. Without this detailed information, assumptions about the reasons animals associate with features of habitat cannot be tested.

Keywords

creviceintertidalrocky shoreenvironmental variablesdistributionshelterclimate change
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 90 , Issue 1 , February 2010 , pp. 169 - 192
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

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References

REFERENCES

Ballantine, W.J. (1961) A biologically defined exposure scale for the comparative description of rocky shores. Field Studies 1, 1–19.Google Scholar
Beck, M.W. (1998) Comparison of the measurement and effects of habitat structure on gastropods in rocky intertidal and mangrove habitats. Marine Ecology Progress Series 169, 165–178.CrossRefGoogle Scholar
Bergey, E.A. (2005) How protective are refuges? Quantifying algal protection in rock crevices. Freshwater Biology 50, 1163–1177.CrossRefGoogle Scholar
Boller, M.L. and Carrington, E. (2006) In situ measurements of hydrodynamic forces imposed on Chondrus crispus Stackhouse. Journal of Experimental Marine Biology and Ecology 337, 159–170.CrossRefGoogle Scholar
Branch, G.M. (1984) Competition between marine organisms—ecological and evolutionary implications. Oceanography and Marine Biology 22, 429–593.Google Scholar
Buckley, B.A., Owen, M.E. and Hofmann, G.E. (2001) Adjusting the thermostat: the threshold induction temperature for the heatshock response in intertidal mussels (genus Mytilus) changes as a function of thermal history. Journal of Experimental Biology 204, 3571–3579.CrossRefGoogle ScholarPubMed
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, 1–12.CrossRefGoogle Scholar
Catesby, S.M. and McKillup, S.C. (1998) The importance of crevices to the intertidal snail Littoraria articulata (Philippi) in a tropical mangrove forest. Hydrobiologia 367, 131–138.CrossRefGoogle Scholar
Clarke, K.R. and Warwick, R.M. (2001) Change in marine communities: an approach to statistical analysis and interpretation. Plymouth, UK: PRIMER-E, 172 pp.Google Scholar
Cleugh, H.A. (2002) Field measurements of windbreak effects on airflow, turbulent exchanges and microclimates. Australian Journal of Experimental Agriculture 42, 665–677.CrossRefGoogle Scholar
Crisp, D.J. (1964) The effects of the severe winter of 1962–63 on marine life in Britain. Journal of Animal Ecology 33, 165–210.CrossRefGoogle Scholar
Denny, M. and Gaylord, B. (2002) The mechanics of wave-swept algae. Journal of Experimental Biology 205, 1355–1362.CrossRefGoogle ScholarPubMed
Denny, M.W. (1983) A simple device for recording the maximum force exerted on intertidal organisms. Limnology and Oceanography 28, 1269–1274.CrossRefGoogle Scholar
Denny, M.W. (1993) Air and water: the biology and physics of life's media. Princeton, NJ: Princeton University Press.CrossRefGoogle Scholar
Denny, M.W., Daniel, T.L. and Koehl, M.A.R. (1985) Mechanical limits to size in wave swept organisms. Ecological Monographs 55, 69–102.CrossRefGoogle Scholar
Denny, M.W., Helmuth, B., Leonard, G.H., Harley, C.D.G., Hunt, L.J.H. and Nelson, E.K. (2004) Quantifying scale in ecology: lessons from a wave-swept shore. Ecological Monographs 74, 513–532.CrossRefGoogle Scholar
Denny, M.W., Miller, L.P. and Harley, C.D.G. (2006) Thermal stress on intertidal limpets: long-term hindcasts and lethal limits. Journal of Experimental Biology 209, 2420–2431.CrossRefGoogle ScholarPubMed
Denny, M.W., Miller, L.P., Stokes, M.D., Hunt, L.J.H. and Helmuth, B.S.T. (2003) Extreme water velocities: topographical amplification of wave-induced flow in the surf zone of rocky shores. Limnology and Oceanography 48, 1–8.CrossRefGoogle Scholar
Denny, M.W. and Paine, R.T. (1998) Celestial mechanics, sea-level changes, and intertidal ecology. Biological Bulletin. Marine Biological Laboratory, Woods Hole 194, 108–115.CrossRefGoogle ScholarPubMed
Diesel, R. and Horst, D. (1995) Breeding in a snail shell—ecology and biology of the Jamaican montane crab Sesarma jarvisi (Decapoda, Grapsidae). Journal of Crustacean Biology 15, 179–195.CrossRefGoogle Scholar
Duffy, J.E. and Hay, M.E. (1991) Food and shelter as determinants of food choice by an herbivorous marine amphipod. Ecology 72, 1286–1298.CrossRefGoogle Scholar
Emson, R.H. and Faller-Fritsch, R.J. (1976) An experimental investigation into the effect of crevice availability on abundance and size-structure in a population of Littorina rudis (Maton): Gastropoda: Prosobranchia. Journal of Experimental Marine Biology and Ecology 23, 285–297.CrossRefGoogle Scholar
Fairweather, P.G. (1988) Movements of intertidal whelks (Morula marginalba and Thais orbita) in relation to availability of prey and shelter. Marine Biology 100, 63–68.CrossRefGoogle Scholar
Fitzhenry, T., Halpin, P.M. and Helmuth, B. (2004) Testing the effects of wave exposure, site, and behaviour on intertidal mussel body temperatures: applications and limits of temperature logger design. Marine Biology 145, 339–349.CrossRefGoogle Scholar
Garrity, S.D. (1984) Some adaptations of gastropods to physical stress on a tropical rocky shore. Ecology 65, 559–574.CrossRefGoogle Scholar
Gaylord, B. (1999) Detailing agents of physical disturbance: wave-induced velocities and accelerations on a rocky shore. Journal of Experimental Marine Biology and Ecology 239, 85–124.CrossRefGoogle Scholar
Gaylord, B. (2000) Biological implications of surf-zone flow complexity. Limnology and Oceanography 45, 174–188.CrossRefGoogle Scholar
Gaylord, B., Blanchette, C.A. and Denny, M.W. (1994) Mechanical consequences of size in wave-swept algae. Ecological Monographs 64, 287–313.CrossRefGoogle Scholar
Gray, D.R. and Hodgson, A.N. (2004) The importance of a crevice environment to the limpet Helcion pectunculus (Patellidae). Journal of Molluscan Studies 70, 67–72.CrossRefGoogle Scholar
Halpin, P.M., Sorte, C.J., Hofmann, G.E. and Menge, B.A. (2002) Patterns of variation in levels of Hsp70 in natural rocky shore populations from microscales to mesoscales. Integrative and Comparative Biology 42, 815–824.CrossRefGoogle ScholarPubMed
Harley, C.D.G. (2002) Light availability indirectly limits herbivore growth and abundance in a high rocky intertidal community during the winter. Limnology and Oceanography 47, 1217–1222.CrossRefGoogle Scholar
Harley, C.D.G. (2008) Tidal dynamics, topographic orientation, and temperature-mediated mass mortalities on rocky shores. Marine Ecology Progress Series 371, 37–46.CrossRefGoogle Scholar
Harper, K.D. and Williams, G.A. (2001) Variation in abundance and distribution of the chiton Acanthopleura japonica and associated molluscs on a seasonal, tropical, rocky shore. Journal of Zoology 253, 293–300.CrossRefGoogle Scholar
Helmuth, B.S.T. (1998) Intertidal mussel microclimates: predicting the body temperature of a sessile invertebrate. Ecological Monographs 68, 51–74.CrossRefGoogle Scholar
Helmuth, B.S.T. (1999) Thermal biology of rocky intertidal mussels: quantifying body temperatures using climatological data. Ecology 80, 15–34.CrossRefGoogle Scholar
Helmuth, B.S.T. and Denny, M.W. (2003) Predicting wave exposure in the rocky intertidal zone: do bigger waves always lead to larger forces. Limnology and Oceanography 48, 1338–1345.CrossRefGoogle Scholar
Helmuth, B.S.T., Harley, C.D.G., 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, 1015–1017.CrossRefGoogle ScholarPubMed
Helmuth, B.S.T. and Hofmann, G.E. (2001) Microhabitats, thermal heterogeneity, and patterns of physiological stress in the rocky intertidal zone. Biological Bulletin. Marine Biological Laboratory, Woods Hole 201, 374–384.CrossRefGoogle ScholarPubMed
Hofmann, G.E. and Somero, G.N. (1995) Evidence for protein damage at environmental temperatures—seasonal changes in levels of ubiquitin conjugates and Hsp70 in the intertidal mussel Mytilus trossulus. Journal of Experimental Biology 198, 1509–1518.CrossRefGoogle ScholarPubMed
Hughes, R.N. and Elner, R.W. (1979) Tactics of a predator, Carcinus maenas, and morphological responses of the prey, Nucella lapillus. Journal of Animal Ecology 48, 65–78.CrossRefGoogle Scholar
Jones, W.E. and Demetropoulos, A. (1968) Exposure to wave action; measurements of an important ecological parameter on rocky shores of Anglesey. Journal of Experimental Marine Biology and Ecology 2, 46–63.CrossRefGoogle Scholar
Kohn, A.J. and Leviten, P.J. (1976) Effect of habitat complexity on population density and species richness in tropical intertidal predatory gastropod assemblages. Oecologia 25, 199–210.CrossRefGoogle ScholarPubMed
Marchetti, K.E. and Geller, J.B. (1987) The effects of aggregation and microhabitat on desiccation and body-temperature of the black turban snail, Tegula funebralis (A. Adams, 1855). Veliger 30, 127–133.Google Scholar
McMahon, R.F. (1990) Thermal tolerance, evaporative water-loss, air-water oxygen-consumption and zonation of intertidal prosobranchs—a new synthesis. Hydrobiologia 193, 241–260.CrossRefGoogle Scholar
Menge, B.A. and Branch, G.M. (2001) Rocky intertidal communities. In Bertness, M.D., Gaines, S.D. and Hay, M.E. (eds) Marine community ecology. Sunderland, MA: Sinauer Associates, pp. 221–251.Google Scholar
Miller, L.P., Harley, C.D.G. and Denny, M.W. (2009) The role of temperature and desiccation stress in limiting the local-scale distribution of the owl limpet, Lottia gigantea. Functional Ecology 23, 756–767.CrossRefGoogle Scholar
Moran, M.J. (1985) The timing and significance of sheltering and foraging behaviour of the predatory intertidal gastropod Morula marginalba Blainville (Muricidae). Journal of Experimental Marine Biology and Ecology 93, 103–114.CrossRefGoogle Scholar
Murphy, R.J., Tolhurst, T.J., Chapman, M.G. and Underwood, A.J. (2005a) Estimation of surface chlorophyll-a on an emersed mudflat using field spectrometry: accuracy of ratios and derivative-based approaches. International Journal of Remote Sensing 26, 1835–1859.CrossRefGoogle Scholar
Murphy, R.J., Underwood, A.J. and Pinkerton, M.H. (2006) Quantitative imaging to measure photosynthetic biomass on an intertidal rock-platform. Marine Ecology Progress Series 312, 45–55.CrossRefGoogle Scholar
Murphy, R.J., Underwood, A.J., Pinkerton, M.H. and Range, P. (2005b) Field spectrometry: new methods to investigate epilithic micro-algae on rocky shores. Journal of Experimental Marine Biology and Ecology 325, 111–124.CrossRefGoogle Scholar
O'Donnell, M.J. (2008) Reduction of wave forces within bare patches in mussel beds. Marine Ecology Progress Series 362, 157–167.CrossRefGoogle Scholar
O'Donnell, M.J. and Denny, M.W. (2008) Hydrodynamic forces and surface topography: centimeter-scale spatial variation in wave forces. Limnology and Oceanography 53, 579–588.CrossRefGoogle Scholar
Paine, R.T. (1980) Food webs: linkage, interaction strength and community infrastructure. Journal of Animal Ecology 49, 667–685.CrossRefGoogle Scholar
Paine, R.T. and Levin, S.A. (1981) Intertidal landscapes—disturbance and the dynamics of pattern. Ecological Monographs 51, 145–178.CrossRefGoogle Scholar
Pardo, L.M. and Johnson, L.E. (2004) Activity and shelter use of an intertidal snail: effects of sex, reproductive condition and tidal cycle. Journal of Experimental Marine Biology and Ecology 301, 175–191.CrossRefGoogle Scholar
Raffaelli, D. and Hawkins, S.J. (1996) Intertidal ecology. London: Chapman & Hall.CrossRefGoogle Scholar
Raffaelli, D.G. and Hughes, R.N. (1978) Effects of crevice size and availability on populations of Littorina rudis and Littorina neritoides. Journal of Animal Ecology 47, 71–83.CrossRefGoogle Scholar
Ruban, A.V. and Horton, P. (1995) Regulation of nonphotochemical quenching of chlorophyll fluorescence in plants. Australian Journal of Plant Physiology 22, 221–230.Google Scholar
Savitzky, A. and Golay, M.J.E. (1964) Smoothing and differentiation of data by simplified least squares procedures. Analytical Chemistry 36, 1627–1639.CrossRefGoogle Scholar
Shimizu, N., Sakai, Y., Hashimoto, H. and Gushima, K. (2006) Terrestrial reproduction by the air-breathing fish Andamia tetradactyla (Pisces; Blenniidae) on supralittoral reefs. Journal of Zoology 269, 357–364.CrossRefGoogle Scholar
Siivonen, Y. and Wermundsen, T. (2008) Characteristics of winter roosts of bat species in southern Finland. Mammalia 72, 50–56.CrossRefGoogle Scholar
Stafford, R. and Davies, M.S. (2004) Temperature and desiccation do not affect aggregation behaviour in high shore littorinids in north-east England. Journal of Negative Results 1, 16–20.Google Scholar
Stephenson, T.A. and Stephenson, A. (1972) Life between tidemarks on rocky shores. San Francisco: W.H. Freeman and Company.Google Scholar
Strasser, M., Reinwald, T. and Reise, K. (2001) Differential effects of the severe winter of 1995/96 on the intertidal bivalves Mytilus edulis, Cerastoderma edule and Mya arenaria in the Northern Wadden Sea. Helgoland Marine Research 55, 190–197.CrossRefGoogle Scholar
Takada, Y. (1999) Influence of shade and number of boulder layers on mobile organisms on a warm temperate boulder shore. Marine Ecology Progress Series 189, 171–179.CrossRefGoogle Scholar
Thompson, T.L. and Glenn, E.P. (1994) Plaster standards to measure water motion. Limnology and Oceanography 39, 1768–1779.CrossRefGoogle Scholar
Underwood, A.J. (1975) Comparative studies on biology of Nerita atramentosa Reeve, Bembicium nanum (Lamarck) and Cellana tramoserica (Sowerby) (Gastropoda-Prosobranchia) in SE Australia. Journal of Experimental Marine Biology and Ecology 18, 153–172.CrossRefGoogle Scholar
Underwood, A.J. (1984) The vertical-distribution and seasonal abundance of intertidal microalgae on a rocky shore in New South Wales. Journal of Experimental Marine Biology and Ecology 78, 199–220.CrossRefGoogle Scholar
Underwood, A.J. (2000) Experimental ecology of rocky intertidal habitats: what are we learning? Journal of Experimental Marine Biology and Ecology 250, 51–76.CrossRefGoogle ScholarPubMed
Underwood, A.J. and Chapman, M.G. (1989) Experimental analyses of the influences of topography of the substratum on movements and density of an intertidal snail, Littorina unifasciata. Journal of Experimental Marine Biology and Ecology 134, 175–196.CrossRefGoogle Scholar
Underwood, A.J. and Chapman, M.G. (1996) Scales of spatial patterns of distribution of intertidal invertebrates. Oecologia 107, 212–224.CrossRefGoogle ScholarPubMed
Underwood, A.J. and Chapman, M.G. (2000) Variation in abundances of intertidal populations: consequences of extremities of environment. Hydrobiologia 426, 25–36.CrossRefGoogle Scholar
Werner, E.E., Gilliam, J.F., Hall, D.J. and Mittelbach, G.G. (1983) An experimental test of the effects of predation risk on habitat use in fish. Ecology 64, 1540–1548.CrossRefGoogle Scholar
Whitcraft, C.R. and Levin, L.A. (2007) Regulation of benthic algal and animal communities by salt marsh plants: Impact of shading. Ecology 88, 904–917.CrossRefGoogle ScholarPubMed
Williams, G.A. and Morritt, D. (1995) Habitat partitioning and thermal tolerance in a tropical limpet, Cellana grata. Marine Ecology Progress Series 124, 89–103.CrossRefGoogle Scholar