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Chapter 20 - Overview and Synthesis

Published online by Cambridge University Press:  07 September 2019

Stephen J. Hawkins
Affiliation:
Marine Biological Association of the United Kingdom, Plymouth
Katrin Bohn
Affiliation:
Natural England
Louise B. Firth
Affiliation:
University of Plymouth
Gray A. Williams
Affiliation:
The University of Hong Kong
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Summary

This volume has achieved a large coverage of the experimentally well-studied areas of the temperate and subtropical coasts of the world (see Figure 1.1) – venturing into the tropics in some regions (Chapter 14, South-East Asia) and including mangroves (Chapter 17). Coral reef systems have not been considered. Much of the emphasis has been on rocky habitats as this is where the majority of experimental work on interactions has been done (but see Chapter 6). As well as reviewing regions where there has been a long history of experimental research (e.g., Chapters 2–4, 6, 10, 11, 13, 15, 16), areas of emerging experimental research in the last twenty-five years (e.g., Chapter 8, western Mediterranean; Chapter 12, south-east Pacific) and understudied regions (e.g., Chapter 7, Argentina; Chapter 14, South-East Asia) have also been included, allowing more comprehensive insights into the processes important for shaping these communities. In this short synthesis chapter, we first consider the main processes determining patterns covered by the previous chapters. We then consider major human impacts in these regions. Finally, we identify gaps in knowledge and make some suggestions for the way forward. We make the case for combining phylogeographic studies with macro-ecology and biogeography, coupled with well-designed hypothesis testing experiments, to better understand processes generating patterns on micro-evolutionary (hundreds to thousands of years) and ecological (up to hundreds of years) time scales.

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Chapter
Information
Interactions in the Marine Benthos
Global Patterns and Processes
, pp. 488 - 505
Publisher: Cambridge University Press
Print publication year: 2019

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References

Altieri, A. H., van Wesenbeeck, B. K., Bertness, M. D, and Silliman, B. R. (2010). Facilitation cascade drives positive relationship between native biodiversity and invasion success. Ecology, 91 (5), 1269–75.CrossRefGoogle Scholar
Arenas, F., Sanchez, I., Hawkins, S. J. and Jenkins, S. R. (2006). The invasibility of marine algal assemblages: role of functional diversity and identity. Ecology, 87, 2851–61.CrossRefGoogle Scholar
Bakun, A. (1990). Global climate change and intensification of coastal ocean upwelling. Science, 247 (4939), 198201.CrossRefGoogle Scholar
Bates, A. E., Helmuth, B., Burrows, M. T. et al. (2018). Biologists ignore ocean weather at their peril. Nature, 560, 299301.CrossRefGoogle Scholar
Bell, E. C. and Denny, M. W. (1994). Quantifying “wave exposure”: a simple device for recording maximum velocity and results of its use at several field sites. Journal of Experimental Marine Biology and Ecology, 181 (1), 929.CrossRefGoogle Scholar
Bertness, M. D. (1989). Intraspecific competition and facilitation in a northern acorn barnacle population. Ecology, 70 (1), 257–68.CrossRefGoogle Scholar
Bertness, M. D. and Callaway, R. (1994). Positive interactions in communities. Trends in Ecology & Evolution, 9 (5), 191–3.CrossRefGoogle Scholar
Bertness, M. D. and Shumway, S. W. (1993). Competition and facilitation in marsh plants. The American Naturalist, 142 (4), 718–24.CrossRefGoogle Scholar
Bishop, M. J., Fraser, J. and Gribben, P. E. (2013). Morphological traits and density of foundation species modulate a facilitation cascade in Australian mangroves. Ecology, 94 (9), 1927–36.CrossRefGoogle Scholar
Boaventura, D., Alexander, M., Della Santina, P. et al. (2002). The effects of grazing on the distribution and composition of low-shore algal communities on the central coast of Portugal and on the southern coast of Britain. Journal of Experimental Marine Biology and Ecology, 267, 185206.CrossRefGoogle Scholar
Bosman, A. L., Hockey, P. A. and Underhill, L. G. (1989). Oystercatcher predation and limpet mortality: the importance of refuges in enhancing the reproductive output of prey populations. Veliger, 32, 120–9.Google Scholar
Bowen, M., Markham, J., Sutton, P. et al. (2017). Interannual variability of sea surface temperature in the southwest Pacific and the role of ocean dynamics. Journal of Climate, 30 (18), 7481–92.CrossRefGoogle Scholar
Broitman, B. R., Blanchette, C. A., Menge, B. A. and Lubchenco, J. (2008). Spatial and temporal patterns of invertebrate recruitment along the west coast of the United States. Ecological Monographs, 78 (3), 403–21.CrossRefGoogle Scholar
Bruno, J. F., Stachowicz, J. J. and Bertness, M. D. (2003). Inclusion of facilitation into ecological theory. Trends in Ecology & Evolution, 18 (3), 119–25.CrossRefGoogle Scholar
Burrows, M. T., Harvey, R., Robb, L. et al. (2009). Spatial scales of variance in distributions of intertidal species on complex coastlines: effects of region, dispersal mode and trophic level. Ecology, 90 (5), 1242–54.CrossRefGoogle Scholar
Burrows, M. T. and Hawkins, S. J. (1998). Modelling patch dynamics on rocky shores using deterministic cellular automata. Marine Ecology Progress Series, 167, 113.CrossRefGoogle Scholar
Burrows, M. T., Jenkins, S. R., Robb, L. and Harvey, R. (2010). Spatial variation in size and density of adult and post-settlement Semibalanus balanoides: disentangling effects of oceanography and local conditions. Marine Ecology Progress Series, 398, 207–19.CrossRefGoogle Scholar
Chan, B. K., Lima, F. P., Williams, G. A., Seabra, R. and Wang, H. Y. (2016). A simplified biomimetic temperature logger for recording intertidal barnacle body temperatures. Limnology and Oceanography: Methods, 14 (7), 448–55.Google Scholar
Chapman, J. W., Carlton, J. T., Bellinger, M. R. and Blakeslee, A. M. (2007). Premature refutation of a human-mediated marine species introduction: the case history of the marine snail Littorina littorea in the Northwestern Atlantic. Biological Invasions, 9 (8), 9951008.CrossRefGoogle Scholar
Chee, S. Y., Othman, A. G., Sim, Y. K., Adam, A. N. M. and Firth, L. B. (2017). Land reclamation and artificial islands: walking the tightrope between development and conservation. Global Ecology and Conservation, 12, 8095.CrossRefGoogle Scholar
Chiswell, S. M., Bostock, H. C., Sutton, P. J. and Williams, M. J. (2015). Physical oceanography of the deep seas around New Zealand: a review. New Zealand Journal of Marine and Freshwater Research, 49 (2), 286317.CrossRefGoogle Scholar
Coleman, R. A., Goss-Custard, J. D., dit Durell, S. E. L. V. and Hawkins, S. J. (1999). Limpet Patella spp. consumption by oystercatchers Haematopus ostralegus: a preference for solitary prey items. Marine Ecology Progress Series, 183, 253–61.CrossRefGoogle Scholar
Coleman, R. A., Underwood, A. J., Benedetti-Cecchi, L. et al. (2006). A continental scale evaluation of the role of limpet grazing on rocky shores. Oecologia, 147, 556–64.CrossRefGoogle Scholar
Connell, J. H. (1961). The influence of interspecific competition and other factors on the distribution of the barnacle Chthamalus stellatus. Ecology, 42, 710–23.CrossRefGoogle Scholar
Connell, S. D. (2007). Water Quality and the Loss of Coral Reefs and Kelp Forests: Alternative States and the Influence of Fishing. Oxford University Press, Melbourne, pp. 556–68.Google Scholar
Cooley, S. R., Cheney, J. E., Kelly, R. P. and Allison, E. H. (2017). Ocean acidification and Pacific oyster larval failures in the Pacific Northwest United States. In Global Change in Marine Systems: Societal and Governing Responses. Routledge, Abingdon.Google 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 (1), 157203.CrossRefGoogle Scholar
Denny, M. W., Dowd, W. W., Bilir, L. and Mach, K. J. (2011). Spreading the risk: small-scale body temperature variation among intertidal organisms and its implications for species persistence. Journal of Experimental Marine Biology and Ecology, 400 (1–2), 175–90.CrossRefGoogle Scholar
Dong, Y.-W., Huang, X.-W., Wang, W., Li, Y. and Wang, J. (2016). The marine ‘great wall’ of China: local and broad-scale ecological impacts of coastal infrastructure on intertidal macrobenthic communities. Diversity and Distribution, 22, 731–44.CrossRefGoogle Scholar
Emmerson, M. C., Solan, M., Emes, C., Paterson, D. M. and Raffaelli, D. (2001). Consistent patterns and the idiosyncratic effects of biodiversity in marine ecosystems. Nature, 411 (6833), 73.CrossRefGoogle Scholar
Ferreira, J. G., Hawkins, S. J. and Jenkins, S. R. (2015). Physical and biological control of fucoid recruitment in range edge and range centre populations. Marine Ecology Progress Series, 518, 8594.CrossRefGoogle Scholar
Figurski, J. D., Malone, D., Lacy, J. R. and Denny, M. (2011). An inexpensive instrument for measuring wave exposure and water velocity. Limnology and Oceanography: Methods, 9 (5), 204–14.Google Scholar
Firth, L. B., Crowe, T. P., Moore, P., Thompson, R. C. and Hawkins, S. J. (2009). Predicting impacts of climate‐induced range expansion: an experimental framework and a test involving key grazers on temperate rocky shores. Global Change Biology, 15 (6), 1413–22.CrossRefGoogle Scholar
Firth, L. B., Knights, A. M., Bridger, D. et al. (2016). Ocean Sprawl: Challenges and Opportunities for Biodiversity Management in a Changing World. In Oceanography and Marine Biology. CRC Press, Boca Raton, FL, pp. 201–78.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 (1–2), 70–5.CrossRefGoogle Scholar
Fitch, J. E. and Crowe, T. P. (2011). Combined effects of temperature, inorganic nutrients and organic matter on ecosystem processes in intertidal sediments. Journal of Experimental Marine Biology and Ecology, 400 (1–2), 257–63.CrossRefGoogle Scholar
Fitzhenry, T., Halpin, P. M. and Helmuth, B. (2004). Testing the effects of wave exposure, site, and behavior on intertidal mussel body temperatures: applications and limits of temperature logger design. Marine Biology, 145 (2), 339–49.CrossRefGoogle Scholar
Folland, C. K., Renwick, J. A., Salinger, M. J. and Mullan, A. B. (2002). Relative influences of the interdecadal Pacific oscillation and ENSO on the South Pacific convergence zone. Geophysical Research Letters, 29 (13), 21-1.CrossRefGoogle Scholar
Gaylord, B. and Gaines, S. D. (2000). Temperature or transport? Range limits in marine species mediated solely by flow. The American Naturalist, 155 (6), 769–89.CrossRefGoogle Scholar
Genner, M. J., Sims, D. W., Southward, A. J. et al. (2010). Body size‐dependent responses of a marine fish assemblage to climate change and fishing over a century‐long scale. Global Change Biology, 16 (2), 517–27.CrossRefGoogle Scholar
Gordon, J. M. and Knights, A. M. (2018). Revisiting Connell: competition but not as we know it. Journal of the Marine Biological Association of the United Kingdom, 98 (6), 1253–61.CrossRefGoogle Scholar
Grevemeyer, I., Herber, R. and Essen, H. H. (2000). Microseismological evidence for a changing wave climate in the northeast Atlantic Ocean. Nature, 408 (6810), 349.CrossRefGoogle Scholar
Gribben, P. E., Kimbro, D. L., Vergés, A. et al. (2017). Positive and negative interactions control a facilitation cascade. Ecosphere, 8 (12), e02065.CrossRefGoogle Scholar
Griffin, J. N., De La Haye, K. L., Hawkins, S. J., Thompson, R. C. and Jenkins, S. R. (2008). Predator diversity and ecosystem functioning: density modifies the effect of resource partitioning. Ecology, 89 (2), 298305.CrossRefGoogle Scholar
Griffin, J. N., Laure, M. L. N., Crowe, T. P. et al. (2010). Consumer effects on ecosystem functioning in rock pools: roles of species richness and composition. Marine Ecology Progress Series, 420, 4556.CrossRefGoogle Scholar
Hallegraeff, G. M. (2010). Ocean climate change, phytoplankton community responses, and harmful algal blooms: a formidable predictive challenge. Journal of Phycology, 46 (2), 220–35.CrossRefGoogle Scholar
Hatton, H. (1938). Essais de bionomie explicative sur quelques especes intercotidales d’algues et d’animaux. Annls Inst Oceanogr Monaco, 17, 241348.Google Scholar
Hawkins, S. J., Evans, A. J., Mieszkowska, N. et al. (2017). Distinguishing globally-driven changes from regional-and local-scale impacts: the case for long-term and broad-scale studies of recovery from pollution. Marine Pollution Bulletin, 124 (2), 573–86.CrossRefGoogle Scholar
Hawkins, S. J. and Hartnoll, R. G. (1983a). Grazing of intertidal algae by marine invertebrates. Oceanography and Marine Biology: An Annual Review, 21, 195282.Google Scholar
Hawkins, S. J. and Hartnoll, R. G. (1983b). Changes in a rocky shore community: an evaluation of monitoring. Marine Environmental Research, 9, 131–81.CrossRefGoogle Scholar
Hawkins, S. J., Hartnoll, R. G., Kain, J. M. and Norton, T. A. (1992). Plant–Animal Interactions on Hard Substrata in the Northeast Atlantic. In John, D. M., Hawkins, S. J. and Price, J. H., eds. Plant-Animal Interactions in the Marine Benthos. Oxford University Press, Oxford, pp. 132.Google Scholar
Hawkins, S. J., Mieszkowska, N., Firth, L. B. et al. (2016). Looking backwards to look forwards: the role of natural history in temperate reef ecology. Marine and Freshwater Research, 67 (1), 113.CrossRefGoogle Scholar
Hawkins, S. J., Moore, P., Burrows, M. T. et al. (2008). Complex interactions in a rapidly changing world: responses of rocky shore communities to recent climate change. Climate Research, 37, 123–33.CrossRefGoogle Scholar
Hawkins, S. J., Sugden, H. E., Mieszkowska, N. et al. (2009). Consequences of climate driven biodiversity changes for ecosystem functioning of North European Rocky Shores. Marine Ecology Progress Series, 396, 245–59.CrossRefGoogle Scholar
Helmuth, B., Choi, F., Matzelle, A. et al. (2016). Long-term, high frequency in-situ measurements of intertidal mussel bed temperatures using biomimetic sensors. Scientific Data, 3, 160087.CrossRefGoogle Scholar
Helmuth, B., Russell, B. D., Connell, S. D. et al. (2014). Beyond long-term averages: making biological sense of a rapidly changing world. Climate Change Responses, 1 (1), 6.CrossRefGoogle Scholar
Jenkins, S. R., Åberg, P., Cervin, G. et al. (2000). Spatial and temporal variation in settlement and recruitment of the intertidal barnacle Semibalanus balanoides (L.)(Crustacea: Cirripedia) over a European scale. Journal of Experimental Marine Biology and Ecology, 243 (2), 209–25.CrossRefGoogle Scholar
Jenkins, S. R., Coleman, R. A., Hawkins, S. J., Burrows, M. T. and Hartnoll, R. G. (2005). Regional scale differences in determinism of grazing effects in the rocky intertidal. Marine Ecology Progress Series, 287, 7786.CrossRefGoogle Scholar
Jenkins, S. R., Moore, P., Burrows, M. T. et al. (2008). Comparative ecology of North Atlantic shores: do differences in players matter for process? Ecology, 89 (sp11), S323.CrossRefGoogle Scholar
Johannesson, K. (1988) The paradox of Rockall: why is a brooding gastropod (Littorina saxatilis) more widespread than one having a planktonic larval dispersal stage (L. littorea)? Marine Biology, 99, 507–13.CrossRefGoogle Scholar
John, D. M., Hawkins, S. J. and Price, J. H., eds. (1992). Plant–Animal Interactions in the Marine Benthos, The Systematics Association Special volume no. 46, Clarendon Press, Oxford.Google Scholar
Johnson, M. P., Burrows, M. T. and Hawkins, S. J. (1998). Individual based simulations of the direct and indirect effects of limpets on a rocky shore Fucus mosaic. Marine Ecology Progress Series, 169, 179–88.CrossRefGoogle Scholar
Jones, C. G., Lawton, J. H. and Shachak, M. (1994). Organisms as Ecosystem Engineers. In Ecosystem Management. Springer, New York, pp. 130–47.Google Scholar
Jonsson, P. R., Granhag, L., Moschella, P. S., Åberg, P., Hawkins, S. J. and Thompson, R. C. (2006). Interactions between wave action and grazing control the distribution of intertidal macroalgae. Ecology, 87 (5), 1169–78.CrossRefGoogle Scholar
Keith, S. A., Roger, J. H., Norton, P. A., Hawkins, S. J. and Newton, A. C. (2011). Individualistic species limitations of climate-induced expansions generated by meso-scale dispersal barriers. Diversity and Distributions, 17, 275–86.CrossRefGoogle Scholar
Kroeker, K. J., Kordas, R. L., Crim, R. et al. (2013). Impacts of ocean acidification on marine organisms: quantifying sensitivities and interaction with warming. Global Change Biology, 19 (6), 1884–96.CrossRefGoogle Scholar
Kuffner, I. B., Andersson, A. J., Jokiel, P. L., Ku‘ulei, S. R. and Mackenzie, F. T. (2008). Decreased abundance of crustose coralline algae due to ocean acidification. Nature Geoscience, 1 (2), 114.CrossRefGoogle Scholar
Lewis, J. R. (1964). The Ecology of Rocky Shores. English Universities Press, London.Google Scholar
Lima, F. P., Gomes, F., Seabra, R. et al. (2016). Loss of thermal refugia near equatorial range limits. Global Change Biology, 22 (1), 254–63.CrossRefGoogle Scholar
Lima, F. P. and Wethey, D. S. (2009). Robolimpets: measuring intertidal body temperatures using biomimetic loggers. Limnology and Oceanography: Methods, 7 (5), 347–53.Google Scholar
Lindberg, D. R., Warheit, K. I. and Estes, J. A. (1987). Prey preference and seasonal predation by oystercatchers on limpets at San Nicolas Island, California, USA. Marine Ecology Progress Series, 39, 105–13.CrossRefGoogle Scholar
Ling, S. D., Scheibling, R. E., Rassweiler, A. et al. (2015). Global regime shift dynamics of catastrophic sea urchin overgrazing. Philosophical Transactions of the Royal Society B, 370 (1659), 20130269.CrossRefGoogle Scholar
McKinney, M. L. and Lockwood, J. L. (1999). Biotic homogenization: a few winners replacing many losers in the next mass extinction. Trends in Ecology & Evolution, 14 (11), 450–3.CrossRefGoogle Scholar
Menge, B. A., Daley, B. A., Lubchenco, J. et al. (1999). Top‐down and bottom‐up regulation of New Zealand rocky intertidal communities. Ecological Monographs, 69 (3), 297330.CrossRefGoogle Scholar
Mills, K. E., Pershing, A. J., Brown, C. J. et al. (2013). Fisheries management in a changing climate: lessons from the 2012 ocean heat wave in the Northwest Atlantic. Oceanography, 26 (2), 191–5.CrossRefGoogle Scholar
Müller, W. A., Frankignoul, C. and Chouaib, N. (2008). Observed decadal tropical Pacific–North Atlantic teleconnections. Geophysical Research Letters, 35 (24).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 (9), 1835–59.CrossRefGoogle Scholar
Murphy, R. J. and Underwood, A. J. (2006). Novel use of digital colour-infrared imagery to test hypotheses about grazing by intertidal herbivorous gastropods. Journal of Experimental Marine Biology and Ecology, 330 (2), 437–47.CrossRefGoogle Scholar
Murphy, R. J., Underwood, A. J. and Jackson, A. C. (2009). Field-based remote sensing of intertidal epilithic chlorophyll: techniques using specialized and conventional digital cameras. Journal of Experimental Marine Biology and Ecology, 380 (1–2), 6876.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 (1), 111–24.CrossRefGoogle Scholar
Ng, T. P., Lau, S. L., Seuront, L. et al. (2017). Linking behaviour and climate change in intertidal ectotherms: insights from littorinid snails. Journal of Experimental Marine Biology and Ecology, 492, 121–31.CrossRefGoogle Scholar
Norton, T. A., Thompson, R. C., Pope, J. et al. (1998). Using confocal laser scanning microscopy, scanning electron microscopy and phase contrast light microscopy to examine marine biofilms. Aquatic Microbial Ecology, 16 (2), 199204.CrossRefGoogle Scholar
O’Connor, N. E. and Crowe, T. P. (2005). Biodiversity loss and ecosystem functioning: distinguishing between number and identity of species. Ecology, 86 (7), 1783–96.Google Scholar
Okumura, Y. M. and Deser, C. (2010). Asymmetry in the duration of El Niño and La Niña. Journal of Climate, 23 (21), 5826–43.CrossRefGoogle Scholar
Paine, R. T. (1969). A note on trophic complexity and community stability. The American Naturalist, 103 (929), 91–3.CrossRefGoogle Scholar
Pearce, A. F. and Feng, M. (2013). The rise and fall of the “marine heat wave” off Western Australia during the summer of 2010/2011. Journal of Marine Systems, 111, 139–56.Google Scholar
Poloczanska, E. S., Hawkins, S. J., Southward, A. J. and Burrows, M. T. (2008). Modelling the response of populations of competing species to climate change. Ecology, 89 (11), 3138–49.CrossRefGoogle Scholar
Poore, A. G., Campbell, A. H., Coleman, R. A. et al. (2012). Global patterns in the impact of marine herbivores on benthic primary producers. Ecology Letters, 15 (8), 912–22.CrossRefGoogle Scholar
Raffaelli, D. and Hawkins, S. J. (1996). Intertidal Ecology. Springer Science & Business Media, Amsterdam.CrossRefGoogle Scholar
Rahmstorf, S. (2007). A semi-empirical approach to projecting future sea-level rise. Science, 315 (5810), 368–70.CrossRefGoogle Scholar
Rilov, G. and Schiel, D. R. (2006a). Seascape‐dependent subtidal-intertidal trophic linkages. Ecology, 87 (3), 731–44.CrossRefGoogle Scholar
Rilov, G. and Schiel, D. R. (2006b). Trophic linkages across seascapes: subtidal predators limit effective mussel recruitment in rocky intertidal communities. Marine Ecology Progress Series, 327, 8393.CrossRefGoogle Scholar
Saintilan, N., Wilson, N. C., Rogers, K., Rajkaran, A. and Krauss, K. W. (2014). Mangrove expansion and salt marsh decline at mangrove poleward limits. Global Change Biology, 20 (1), 147–57.CrossRefGoogle Scholar
Salinger, M. J., Renwick, J. A. and Mullan, A. B. (2001). Interdecadal Pacific oscillation and south Pacific climate. International Journal of Climatology, 21 (14), 1705–21.CrossRefGoogle Scholar
Sanz-Lázaro, C., Rindi, L., Maggi, E., Dal Bello, M. and Benedetti-Cecchi, L. (2015). Effects of grazer diversity on marine microphytobenthic biofilm: a ‘tug of war’ between complementarity and competition. Marine Ecology Progress Series, 540, 145–55.CrossRefGoogle Scholar
Sarà, G., Kearney, M. and Helmuth, B. (2011). Combining heat-transfer and energy budget models to predict thermal stress in Mediterranean intertidal mussels. Chemistry and Ecology, 27 (2), 135–45.CrossRefGoogle Scholar
Schiel, D. R. and Foster, M. S. (2015). The Biology and Ecology of Giant Kelp Forests. University of California Press, Berkeley.CrossRefGoogle Scholar
Schiel, D. R. and Howard-Williams, C. (2016). Controlling inputs from the land to sea: limit-setting, cumulative impacts and ki uta ki tai. Marine and Freshwater Research, 67 (1), 5764.CrossRefGoogle Scholar
Seabra, R., Wethey, D. S., Santos, A. M. and Lima, F. P. (2011). Side matters: microhabitat influence on intertidal heat stress over a large geographical scale. Journal of Experimental Marine Biology and Ecology, 400 (1–2), 200–8.CrossRefGoogle Scholar
Silva, A. C. F., Boaventura, D. M., Thompson, R. C. and Hawkins, S. J. (2014). Spatial and temporal patterns of subtidal and intertidal crabs excursions. Journal of Sea Research, 85, 343–8.CrossRefGoogle Scholar
Silva, A. C. F., Hawkins, S. J., Boaventura, D. M., Brewster, E. and Thompson, R. C. (2010). Use of the intertidal zone by mobile predators: influence of wave exposure, tidal phase and elevation on abundance and diet. Marine Ecology Progress Series, 406, 197210.CrossRefGoogle Scholar
Silva, A. C. F., Hawkins, S. J., Boaventura, D. M. and Thompson, R. C. (2008). Predation by small mobile aquatic predators regulates populations of the intertidal limpet Patella vulgata (L.). Journal of Experimental Marine Biology and Ecology, 367 (2), 259–65.CrossRefGoogle Scholar
Skov, M. W., Hawkins, S. J., Volkelt-Igoe, M., Pike, J., Thompson, R. C. and Doncaster, C. P. (2011). Patchiness in resource distribution mitigates habitat loss: insights from high‐shore grazers. Ecosphere, 2 (5), 117.CrossRefGoogle Scholar
Smayda, T. J. (2000). Ecological features of harmful algal blooms in coastal upwelling ecosystems. African Journal of Marine Science, 22, 219–53.Google Scholar
Southgate, T., Wilson, K., Cross, T. F. and Myers, A. A. (1984). Recolonization of a rocky shore in SW Ireland following a toxic bloom of the dinoflagellate, Gyrodinium aureolum. Journal of the Marine Biological Association of the United Kingdom, 64 (2), 485–92.CrossRefGoogle Scholar
Stephenson, T. A. and Stephenson, A. (1949). The universal features of zonation between tide-marks on rocky coasts. The Journal of Ecology, 37, 289305.CrossRefGoogle Scholar
Stephenson, T. A. and Stephenson, A. (1972). Life between Tidemarks on Rocky Shores. W. H. Freeman, San Francisco, CA.Google Scholar
Thompson, R. C., Norton, T. A. and Hawkins, S. J. (2004). Physical stress and biological control regulate the producer–consumer balance in intertidal biofilms. Ecology, 85 (5), 1372–82.CrossRefGoogle Scholar
Thomsen, M. S., Metcalfe, I., South, P. and Schiel, D. R. (2016). A host-specific habitat former controls biodiversity across ecological transitions in a rocky intertidal facilitation cascade. Marine and Freshwater Research, 67 (1), 144–52.CrossRefGoogle Scholar
Trudgill, S. T., Smart, P. L., Friederich, H. and Crabtree, R. W. (1987). Bioerosion of intertidal limestone, Co. Clare, Eire – 1: Paracentrotus lividus. Marine Geology, 74 (1–2), 8598.CrossRefGoogle Scholar
Underwood, A. J. (1998). Grazing and disturbance: an experimental analysis of patchiness in recovery from a severe storm by the intertidal alga Hormosira banksii on rocky shores in New South Wales. Journal of Experimental Marine Biology and Ecology, 231 (2), 291306.CrossRefGoogle Scholar
Underwood, A. J. and Fairweather, P. G. (1986). Intertidal communities: do they have different ecologies or different ecologists. Proceedings of the Ecological Society of Australia, 14, 716.Google Scholar
Underwood, A. J. and Jernakoff, P. (1984). The effects of tidal height, wave-exposure, seasonality and rock-pools on grazing and the distribution of intertidal macroalgae in New South Wales. Journal of Experimental Marine Biology and Ecology, 75 (1), 7196.CrossRefGoogle Scholar
Wernberg, T., Smale, D. A., Tuya, F. et al. (2013). An extreme climatic event alters marine ecosystem structure in a global biodiversity hotspot. Nature Climate Change, 3 (1), 78.CrossRefGoogle Scholar
Wethey, D. S., Woodin, S. A., Hilbish, T. J., Jones, S. J., Lima, F. P. and Brannock, P. M. (2011). Response of intertidal populations to climate: effects of extreme events versus long term change. Journal of Experimental Marine Biology and Ecology, 400 (1–2), 132–44.CrossRefGoogle Scholar
Williams, G. A., Helmuth, B., Russell, B. D., Dong, Y. W., Thiyagarajan, V. and Seuront, L. (2016). Meeting the climate change challenge: pressing issues in southern China and SE Asian coastal ecosystems. Regional Studies in Marine Science, 8, 373–81.CrossRefGoogle Scholar
Wood, H. L., Spicer, J. I. and Widdicombe, S. (2008). Ocean acidification may increase calcification rates, but at a cost. Proceedings of the Royal Society of London B, 275 (1644), 1767–73.CrossRefGoogle Scholar
Zhang, S., Han, G. D. and Dong, Y. W. (2014). Temporal patterns of cardiac performance and genes encoding heat shock proteins and metabolic sensors of an intertidal limpet Cellana toreuma during sublethal heat stress. Journal of Thermal Biology, 41, 31–7.CrossRefGoogle Scholar
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Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

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Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

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Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

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