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Chapter 4 - Rocky Intertidal Shores of the North-West Atlantic Ocean

Published online by Cambridge University Press:  07 September 2019

By
Steven R. Dudgeon  and
Peter S. Petraitis
Edited by
Stephen J. Hawkins ,
Katrin Bohn ,
Louise B. Firth  and
Gray A. Williams
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

North-west Atlantic rocky intertidal shores contain few species that are affected by sharp environmental gradients. As a result, these communities have been widely used as a model experimental system. Earlier studies focussed on how average differences in ecological processes can be driven by environmental differences. More recently, there is an emphasis on how variability in recruitment and ecological interactions can shape communities. In this chapter, we explore how these two distinctly different conceptual approaches – average effects versus variability in effects – have affected the course of ecological research. Our review touches on how phylogeographic history, large-scale variability in ecological processes and small-scale indirect interactions have contributed to the generation and maintenance of community patterns. We argue that human activities, including harvesting, introducing non-native species, eutrophication and climate change, are likely to increase the variability of ecological processes. We conclude that variability of ecological processes and human activities vary on a scale much larger or longer than a typical experiment. Future studies should explicitly incorporate scales that capture the role of variability on the resilience of coastal ecosystems.

Keywords

anthropogenic forcingclimate changeinvasive speciesindirect effectsnorth-west Atlanticrocky intertidalvariability
Type
Chapter
Information
Interactions in the Marine Benthos
Global Patterns and Processes
 , pp. 61 - 89
Publisher: Cambridge University Press
Print publication year: 2019

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References

Abrams, P. A., Menge, B. A., Mittelbach, G. G., Spiller, D. and Yodzis, P. (1996). The Role of Indirect Effects in Food Webs. In Polis, G. and Winemiller, K., eds. Food Webs: Dynamics and Structure. Chapman Hall, New York, pp. 371–95.Google Scholar
Adey, W. H. and Steneck, R. S. (2001). Thermogeography over time creates biogeographic regions: a temperature/space/time-integrated model and an abundance-weighted test for benthic marine algae. Journal of Phycology, 37, 677–98.Google Scholar
Bedford Institute of Oceanography. (1987). State of the Ocean: March. Weekly Briefing 24 April 1987. Bedford Institute of Oceanography, Bedford, Nova Scotia.Google Scholar
Bergeron, P. and Bourget, E. (1984). The effect of cold temperatures and ice on intertidal populations in northern regions, particularly in the St. Lawrence estuary. Oceanis, 10, 259–78.Google Scholar
Berlow, E. L. (1999). Strong effects of weak interactions in ecological communities. Nature, 398 , 330–4.CrossRefGoogle Scholar
Bertness, M. D. (1989). Intraspecific competition and facilitation in a northern acorn barnacle population. Ecology, 70, 257–68.CrossRefGoogle Scholar
Bertness, M. D., Leonard, G. H., Levine, J. M., Schmidt, P. R. and Ingraham, A. O. (1999). Testing the relative contribution of positive and negative interactions in rocky intertidal communities. Ecology, 80, 2711–26.CrossRefGoogle Scholar
Bertness, M. D., Trussell, G. C., Ewanchuk, P. J. and Silliman, B. R. (2002). Do alternate stable community states exist in the Gulf of Maine rocky intertidal zone? Ecology, 83 (12), 3434–48.CrossRefGoogle Scholar
Bertness, M. D., Trussell, G. C., Ewanchuk, P. J., Silliman, B. R. and Crain, C. M. (2004a). Consumer-controlled community states on Gulf of Maine rocky shores. Ecology, 85, 1321–31.Google Scholar
Bertness, M. D., Trussell, G. C., Ewanchuk, P. J. and Silliman, B. R. (2004b). Do alternate stable community states exist in the Gulf of Maine rocky intertidal zone? Ecology, 85, 1165–7.Google Scholar
Bertness, M. D., Yund, P. O. and Brown, A. F. (1983). Snail grazing and the abundance of algal crusts on a sheltered New England rocky beach. Journal of Experimental Marine Biology and Ecology, 71, 147–64.Google Scholar
Blakeslee, A. M., Byers, J. E. and Lesser, M. P. (2008). Solving cryptogenic histories using host and parasite molecular genetics: the resolution of Littorina littorea’s North American origin. Molecular Ecology, 17, 3684–96.CrossRefGoogle ScholarPubMed
Boudreau, S. A. and Worm, B. (2010). Top-down control of lobster in the Gulf of Maine: insights from local ecological knowledge and research surveys. Marine Ecology Progress Series, 403, 181–91.CrossRefGoogle Scholar
Bourdeau, P. E. and O’Connor, N. J. (2003). Predation by the nonindigenous Asian shore crab Hemigrapsus sanguineus on macroalgae and molluscs. Northeastern Naturalist, 10, 319–34.Google Scholar
Bourget, E. and Fortin, M. J. (1995). A commentary on current approaches in the aquatic sciences. Hydrobiologia, 300, 1–16.Google Scholar
Bourget, E., Archambault, D. and Bergeron, P. (1985). Effet des proprieties hivernales sur les peuplements epibenthiques intertidaux dans un milieu subarctique, l’estuaire du Saint-Laurent. Le Naturaliste Canadiens, Revue d’Ecologie et de Systématique, 112, 131–42.Google Scholar
Bourque, B. J. (1995). Diversity and Complexity in Prehistoric Maritime Societies: A Gulf of Maine Perspective. Plenum Press, New York.Google Scholar
Bozinovic, F., Bastías, D. A., Boher, F., Clavijo-Baquet, S., Estay, S. A. and Angilletta, M. J. Jr. (2011). The mean and variance of environmental temperature interact to determine physiological tolerance and fitness. Physiological and Biochemical Zoology, 84, 543–52.Google Scholar
Brawley, S. H., Coyer, J. A., Blakeslee, A. M. H. et al. (2009). Historical invasions of the intertidal zone of Atlantic North America associated with distinctive patterns of trade and emigration. Proceedings of the National Academy of Sciences USA, 106, 8239–44.Google Scholar
Breen, E. and Metaxas, A. (2009). Effects of non-indigenous Carcinus maenas on the growth and condition of juvenile Cancer irroratus. Journal of Experimental Marine Biology and Ecology, 377, 12–19.Google Scholar
Briggs, J. (1974). Marine Zoogeography. New York: McGraw-Hill.Google Scholar
Bryson, E. S., Trussell, G. C. and Ewanchuk, P. J. (2014). Broad-scale geographic variation in the organization of rocky intertidal communities in the Gulf of Maine. Ecological Monographs, 84, 579–97.CrossRefGoogle Scholar
Burrows, M., Schoeman, D. S., Buckley, L. B. et al. (2011). The pace of shifting climate in marine and terrestrial ecosystems. Science, 334, 652–5.CrossRefGoogle ScholarPubMed
Carlton, J. (1982). The historical biogeography of Littorina littorea on the Atlantic coast of North America, and implications for the interpretation of the structure of New England intertidal communities. Malacology Review, 15, 146.Google Scholar
Carlton, J. T. and Cohen, A. N. (2003). Episodic global dispersal in shallow water marine organisms: the case history of the European shore crabs Carcinus maenas and C. aestuarii. Journal of Biogeography, 30, 1809–20.Google Scholar
Chapman, A. R. O. and Johnson, C. R. (1990). Disturbance and Organization of Macroalgal Assemblages in the Northwest Atlantic. In Chapman, A. R. O. and Underwood, A. J., eds. Determinants of Structure in Intertidal and Subtidal Macroalgal Assemblages. Kluwer, Dordrecht, pp. 77–121.Google Scholar
Cohen, A. N., Carlton, J. T. and Fountain, M. C. (1995). Introduction, dispersal and potential impacts of the green crab Carcinus maenas in San Francisco Bay, California. Marine Biology, 122(2), 225–37.Google Scholar
Colton, H. S. (1916). On some varieties of Thais lapillus in the Mount Desert region, a study of individual ecology. Proceedings of the Academy of Natural Sciences of Philadelphia, 68, 440–54.Google Scholar
Connell, J. H. (1978). Diversity in tropical rain forests and coral reefs. Science, 199, 1302–10.CrossRefGoogle ScholarPubMed
Connolly, S. R. and Roughgarden, J. (1998). A latitudinal gradient in northeast Pacific intertidal community structure: Evidence for an oceanographically based synthesis of marine community theory. American Naturalist, 151, 311–26.Google Scholar
Cooper, S. R. and Brush, G. S. (1993). A 2,500-year history of anoxia and eutrophication in Chesapeake Bay. Estuaries, 16, 617–26.Google Scholar
Dijkstra, J. Harris, L. G. and Westerman, E. (2007). Distribution and long-term temporal patterns of four invasive colonial ascidians in the Gulf of Maine. Journal of Experimental Marine Biology and Ecology, 342, 61–8.Google Scholar
CLIMAP Project Members. (1976). The surface of the ice-age Earth. Science, 191, 1131–7.Google Scholar
Davison, I. R. (1987). Adaptation of photosynthesis in Laminaria saccharina (Phaeophyta) to change in growth temperature. Journal of Phycology, 23 (2), 273–83.CrossRefGoogle Scholar
Davison, I. R., Greene, R. M. and Podolak, E. J. (1991). Temperature acclimation of respiration and photosynthesis in the brown alga Laminaria saccharina. Marine Biology, 110, 449–54.CrossRefGoogle Scholar
Denny, M. W. (2017). The fallacy of the average: on the ubiquity, utility and continuing novelty of Jensen’s inequality. Journal of Expermintal Biology, 220, 139–46.Google ScholarPubMed
Dernbach, E. M. and Freeman, A. S. (2015). Foraging preference of whelks Nucella lapillus is robust to influences of wave exposure and predator cues. Marine Ecology Progress Series, 540, 135–44.Google Scholar
Dudgeon, S. R. and Petraitis, P. S. (2001). Scale-dependent recruitment and divergence of intertidal communities. Ecology, 82, 991–1006.Google Scholar
Dudgeon, S. R., Kübler, J. E., Vadas, R. L. and Davison, I. R. (1995). Physiological tolerances to environmental variation in intertidal red algae: does thallus morphology matter? Marine Ecology Progress Series, 117, 193–206.Google Scholar
Dudgeon, S. R., Steneck, R. S., Davison, I. R. and Vadas, R. L. (1999). Coexistence of similar species in a space-limited intertidal zone. Ecological Monographs, 69, 331–52.Google Scholar
Easterling, D. R., Meehl, G. A., Parmesan, C., Changnon, S. A., Karl, T. R. and Mearns, L. O. (2000). Climate extremes: observations, modelling, and impacts. Science, 289, 2068–74.Google Scholar
Ellis, J. C., Chen, W., O’Keefe, B., Shulman, M. J. and Witman, J. D. (2005). Predation by gulls on crabs in the rocky intertidal and shallow subtidal zones of the Gulf of Maine. Journal of Experimental Marine Biology and Ecology, 324, 31–43.Google Scholar
Ellis, J. C., Fariña, J. M. and Witman, J. D. (2006). Nutrient transfer from sea to land: the case of gulls and cormorants in the Gulf of Maine. Journal of Animal Ecology, 75, 565–74.Google Scholar
Ellis, J. C., Shulman, M. J., Wood, M., Witman, J. D. and Lozyniak, S. (2007). Regulation of intertidal food webs by avian predators on New England rocky shores. Ecology, 88(4), 853–63.Google Scholar
Epifanio, C. E. (2013). Invasion biology of the Asian shore crab Hemigrapsus sanguineus: a review. Journal of Experimental Marine Biology and Ecology, 441, 33–49.Google Scholar
Fairweather, P. G. (1988). Consequences of supply-side ecology – manipulating the recruitment of intertidal barnacles affects the intensity of predation upon them. Biological Bulletin, 175, 349–54.Google Scholar
Field, C. B., Barros, V., Stocker, T. F. et al. (2012). Managing the Risks of Extreme Events and Disasters to Advance Climate Change Adaptation. In A Special Report of Working Groups I and II of the Intergovernmental Panel on Climate Change. Cambridge University Press, Cambridge.Google Scholar
Fisher, J. A. D. (2005). Exploring ecology’s attic: overlooked ideas on intertidal food webs. Bulletin of the Ecological Society of America, 86, 145–51.Google Scholar
Fisher, J. A. D. (2010). Parasite-like associations in rocky intertidal assemblages: implications for escalated gastropod defences. Marine Ecology Progress Series, 399, 199–209.Google Scholar
Fisher, J. A. D., Rhile, E. C., Liu, H. and Petraitis, P. S. (2009). An intertidal snail shows a dramatic size increase over the past century. Proceedings of the National Academy of Sciences USA, 106, 5209–12.Google Scholar
Fogarty, M. J., Townsend, D. and Klein, E. (2012). Advances in understanding ecosystem structure and function in the Gulf of Maine. American Fisheries Symposium, 79, 261–72.Google Scholar
Freeman, A. S. and Byers, J. E. (2006). Divergent induced responses to an invasive predator in marine mussel populations. Science, 313, 831–3.CrossRefGoogle Scholar
Gaines, S. D. and Denny, M. W. (1993). The largest, smallest, highest, lowest, longest, shortest – extremes in ecology. Ecology, 74 (6), 1677–92.Google Scholar
Garbary, D. J., Galway, M. E. and Halat, L. (2017). Response to Ugarte et al.: Ascophyllum (phaeophyceae) annually contributes over 100% of its vegetative biomass to detritus. Phycologia, 56 (1), 114–16.Google Scholar
Gerard, V. (1988). Ecotypic differentiation in light-related traits of the kelp Laminaria saccharina. Marine Biology, 97 (1), 25–36.CrossRefGoogle Scholar
Glude, J. B. (1955). The effects of temperature and predators on the abundance of the soft-shell clam, Mya arenaria in New England. Transactions of the American Fisheries Society, 84, 12–26.Google Scholar
Grabowski, J. H., Clesceri, E. J., Baukus, E. J., Gaudette, J., Weber, M. and Yund, P. O. (2010). Use of herring bait to farm lobsters in the Gulf of Maine. PLoS ONE, 5, e10188.Google Scholar
Griffen, B. and Byers, J. E. (2009). Community impacts of two invasive crabs: the interactive roles of density, prey recruitment and indirect effects. Biological Invasions, 11 (4), 927–40.Google Scholar
Halat, L., Galway, M. E., Gitto, S. and Garbary, D. J. (2015). Epidermal shedding in Ascophyllum nodosum (Phaeophyceae): seasonality, productivity and relationship to harvesting. Phycologia, 54, 599–608.Google Scholar
Harley, C. D. G. and Paine, R. T. (2009). Contingencies and compounded rare perturbations dictate sudden distributional shifts during periods of gradual climate change. Proceedings of the National Academy of Sciences USA, 106, 11172–6.Google Scholar
Harley, C. D. G., Anderson, K. M., Demes, K. W. et al. (2012). Effects of climate change on global seaweed communities. Journal of Phycology, 48 (5), 1064–78.Google Scholar
Harnish, L. and Willison, J. H. M. (2009). Efficiency of bait usage in the Nova Scotia lobster fisher: a first look. Journal of Cleaner Production, 17, 345–7.Google Scholar
Harris, L. G. and Jones, A. C. (2005). Temperature, herbivory and epibiont acquisition as factors controlling the distribution and ecological role of an invasive seaweed. Biological Invasions 7, 913–24.Google Scholar
Hawkins, S. J., Firth, L. B., McHugh, M. et al. (2013). Data rescue and reuse: recycling old information for new concerns. Marine Policy, 42, 91–8.CrossRefGoogle Scholar
Hawkins, S. J., Evans, A. J., Firth, L. B. 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, 573–86.Google Scholar
Jackson, J. B. C. (2001). What was natural in the coastal oceans? Proceedings of the National Academy of Sciences USA, 98 (10), 5411–18.CrossRefGoogle ScholarPubMed
Jackson, J. B. C., Kirby, M. X. Berger, W. H. et al. (2001). Historical overfishing and the recent collapse of coastal ecosystems. Science, 293, 629–38.Google 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 U.K., 84, 327–9.Google Scholar
Johnson, L. E., Brawley, S. H. and Adey, W. H. (2012). Secondary spread of invasive species: historic patterns and underlying mechanisms of the continuing invasion of the European rockweed Fucus serratus in eastern North America. Biological Invasions, 14, 79–97.Google Scholar
Johnson, D. S. and Skutch, A. F. (1928). Littoral vegetation on a headland of Mt. Desert Island, Maine. II. Tidepools and the environment and classification of submersible plant communities. Ecology, 9, 307–38.Google Scholar
Jones, S. J., Lima, F. P. and Wethey, D. S. (2010). Rising environmental temperatures and biogeography: poleward range contraction of the blue mussel, Mytilus edulis L., in the western Atlantic. Journal of Biogeography, 37, 2243–59.Google Scholar
Jueterbock, A., Tyberghein, L., Verbruggen, H., Coyer, J. A., Olsen, J. L. and Hoarau, G. (2013). Climate change impact on seaweed meadow distribution in the North Atlantic rocky intertidal. Ecology and Evolution, 3 , 1356–73.Google Scholar
Kassen, R., Buckling, A., Bell, G. and Rainey, P. B. (2000). Diversity peaks at intermediate productivity in a laboratory microcosm. Nature, 406, 508–12.Google Scholar
Kelaher, B. P. and Levinton, J. S. (2003). Variation in detrital enrichment causes spatio-temporal variation in soft sediment assemblages. Marine Ecology Progress Series, 261, 85–97.Google Scholar
Keser, M., Swenarton, J. T. and Foertch, J. F. (2005). Effects of thermal input and climate change on growth of Ascophyllum nodosum (Fucales, Phaeophyceae) in eastern Long Island Sound (USA). Journal of Sea Research, 54, 211–20.Google Scholar
Kordas, R. L. and Dudgeon, S. R. (2009). Modelling variation in interaction strength between barnacles and fucoids. Oecologia, 158, 717–31.Google Scholar
Kordas, R. L. and Dudgeon, S. R. (2011). Dynamics of species interaction strength in space, time and with developmental stage. Proceedings of the Royal Society of London B, 278, 1804–13.Google Scholar
Kordas, R. L., Dudgeon, S. R., Storey, S. and Harley, C. D. G. (2015). Intertidal community responses to field-based experimental warming. Oikos, 124, 888–98.Google Scholar
Kraemer, G. P., Sellberg, M., Gordon, A. and Main, J. (2007). Eight-year record of Hemigrapsus sanguineus (Asian shore crab) invasion in western Long Island Sound estuary. Northeastern Naturalist, 14, 207–24.Google 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.Google Scholar
Kübler, J. E. and Davison, I. R. (1993). High-temperature tolerance of photosynthesis in the red alga, Chondrus crispus. Marine Biology, 117, 327–36.Google Scholar
Kübler, J. E. and Davison, I. R. (1995). Thermal acclimation of light-use characteristics of Chondrus crispus (Rhodophyta). European Journal of Phycology, 30, 189–95.Google Scholar
Kübler, J. E. and Dudgeon, S. R. (2015). Predicting effects of ocean acidification and warming on algae lacking carbon-concentrating mechanisms. PLoS ONE, 10 (7), e0132806.Google Scholar
Kübler, J. E., Johnston, A. M. and Raven, J. A. (1999). The effects of reduced and elevated CO2 and O2 on the seaweed, Lomentaria articulata. Plant, Cell & Environment, 22, 1303–10.Google Scholar
Kuebler, J. E., Davison, I. R. and Yarish, C. (1991). Photosynthetic temperature adaptation in the red algae, Lomentaria baileyana and Lomentaria orcadensis. British Phycological Journal, 26, 9–19.CrossRefGoogle Scholar
Large, S. I. and Smee, D. L. (2013). Biogeographic variation in behavioural and morphological responses to predation risk. Oecologia, 171, 961–9.Google Scholar
Leonard, G. H. (2000). Latitudinal variation in species interactions: a test in the New England rocky intertidal zone. Ecology, 81, 1015–30.CrossRefGoogle Scholar
Leonard, G. H., Levine, J. M., Schmidt, P. R. and Bertness, M. D. (1998). Flow-driven variation in intertidal community structure in a Maine estuary. Ecology, 79, 1395–411.Google Scholar
Leonard, G. H., Bertness, M. D. and Yund, P. O. (1999). Crab predation, waterborne cues, and inducible defences in the blue mussel, Mytilus edulis. Ecology, 80 (1), 1–14.Google Scholar
Lesser, M. P. (2016). Climate change stressors cause metabolic depression in the blue mussel, Mytilus edulis, from the Gulf of Maine. Limnology and Oceanography, 61, 1705–17.Google Scholar
Lewis, J. R. (1964). The Ecology of Rocky Shores. English University Press, London.Google Scholar
Lotze, H. K. and Milewski, I. (2004). Two centuries of multiple human impacts and successive changes in a north Atlantic food web. Ecological Applications, 14 (5), 1428–47.CrossRefGoogle Scholar
Lotze, H. K. and Worm, B. (2000). Variable and complementary effects of herbivores on different life stages of bloom-forming macroalgae. Marine Ecology Progress Series, 200, 167–75.CrossRefGoogle Scholar
Lubchenco, J. (1978). Plant species diversity in a marine intertidal community: importance of herbivore food preferences and algal competitive abilities. American Naturalist, 112, 23–39.Google Scholar
Lubchenco, J. (1983). Littorina and Fucus: effects of herbivores, substratum heterogeneity, and plant escapes during succession. Ecology, 64, 1116–23.Google Scholar
Lubchenco, J. and Menge, B. A. (1978). Community development and persistence in a low rocky intertidal zone. Ecological Monographs, 59, 67–94.Google Scholar
Lyons, P. Thornber, C., Portnoy, J. and Gwilliam, E. (2009). Dynamics of macroalgal blooms along the Cape Cod National Seashore. Northeastern Naturalist, 16 (1), 53–63.Google Scholar
Maggs, C. A., Castihlo, R., Foltz, D. et al. (2008). Evaluating signatures of glacial refugia for North Atlantic benthic marine taxa. Ecology, 89 (11), S108–22.Google Scholar
Mann, K. H. (1973). Seaweeds: their productivity and strategy for growth. Science, 182, 975–81.CrossRefGoogle ScholarPubMed
Markham, W. E. (1980). Ice Atlas: Eastern Canadian Seaboard. Canadian Government Publishing Centre, Hull, Quebec.Google Scholar
Martin, T. L. and Huey, R. B. (2008). Why “suboptimal” is optimal: Jensen’s inequality and ectotherm thermal preferences. American Naturalist, 171, E102–18.Google Scholar
Matassa, C. M. and Trussell, G. C. (2014). Prey state shapes the effects of temporal variation in predation risk. Proceedings of the Royal Society of London B, 281, 20141952.Google Scholar
Matassa, C. M. and Trussell, G. C. (2015). Effects of predation risk across a latitudinal temperature gradient. Oecologia, 177, 775–84.Google Scholar
Mathieson, A. C., Dawes, C. J., Pederson, J. Gladych, R. A. and Carlton, J. T. (2008). The Asian red seaweed Grateloupia turuturu (Rhodophyta) invades the Gulf of Maine. Biological Invasions, 10, 985–8.Google Scholar
McCook, L. J. (1992) Species interactions and community structure during succession following massive ice scour of a rocky intertidal seashore. PhD, Dalhousie University.Google Scholar
Meehl, G. A. and Tebaldi, C. (2004). More intense, more frequent, and longer lasting heat waves in the 21st century. Science, 305, 994–7.Google Scholar
Menge, B. A. (1976). Organization of the New England rocky intertidal community: role of predation, competition, and environmental heterogeneity. Ecological Monographs, 46, 355–93.Google Scholar
Menge, B. A. (1983). Components of predation intensity in the low zone of the New England rocky intertidal region. Oecologia, 58, 141–55.Google Scholar
Menge, B. A. and Sutherland, J. P. (1976). Species diversity gradients: Synthesis of roles of predation, competition and temporal heterogeneity. American Naturalist, 110, 351–69.Google Scholar
Menge, B. A. and Sutherland, J. P. (1987). Community regulation: variation in disturbance, competition, and predation in relation to environmental stress and recruitment. American Naturalist, 130, 730–57.Google Scholar
Methratta, E. T. and Petraitis, P. S. (2008). Propagation of scale-dependent effects from recruits to adults in barnacles and seaweeds. Ecology, 89 (11), 3128–37.Google 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, 191–5.Google Scholar
Muhlin, J. F., Coleman, M. A., Rees, T. A. V. and Brawley, S. H. (2011). Modelling of reproduction in the intertidal macrophyte Fucus vesiculosus and implications for spatial subsidies in the nearshore environment. Marine Ecology Progress Series, 440, 79–94.Google Scholar
Myers, R. A. and Worm, B. (2005). Extinction, survival or recovery of large predatory fishes. Philosophical Transactions of the Royal Society B, 360, 13–20.Google Scholar
O’Connor, N. J. (2014). Invasion dynamics on a temperate rocky shore: from early invasion to establishment of a marine invader. Biological Invasions, 16, 73–87.Google Scholar
O’Donnell, M. J., George, M. N. and Carrington, E. (2013). Mussel byssus attachment weakened by ocean acidification. Nature Climate Change, 3 (6), 587–90.Google Scholar
Osman, R. W. and Whitlach, R. B. (2004). The control of the development of a marine benthic community by predation on recruits. Journal of Experimental Marine Biology and Ecology, 311, 117–45.Google Scholar
Osman, R. W. and Whitlach, R. B. (2007). Variation in the ability of Didemnum sp. to invade established communities. Journal of Experimental Marine Biology and Ecology 342, 40–53.CrossRefGoogle Scholar
Paine, R. T. (1966). Food web complexity and species diversity. American Naturalist, 100, 65–75.Google Scholar
Paine, R. T. (1969). A note on trophic complexity and community stability. American Naturalist, 103, 91–3.Google Scholar
Paine, R. T. and Vadas, R. L. (1969). Effects of grazing by sea urchins, Strongylocentrotus spp., on benthic algal populations. Limnology and Oceanography, 14, 710–19.Google Scholar
Palmer, A. R. (1990). Effect of crab effluent and scent of damaged conspecifics on feeding, growth, and shell morphology of the Atlantic dogwhelk Nucella lapillus (L.). Hydrobiologia, 193, 155–82.Google Scholar
Pappal, A. (2010). State of the Gulf of Maine Report: Marine Invasive Species. Massachusetts Office of Coastal Zone Management and Gulf of Maine Council on the Marine Environment, Boston.Google Scholar
Pearson, G. A. and Brawley, S. H. (1998). Control of gamete release in fucoid algae: sensing hydrodynamic conditions via carbon acquisition. Ecology 79 (5), 1725–39.Google Scholar
Pershing, A. J., Alexander, M., Hernandez, C. M. et al. (2015). Slow adaptation in the face of rapid warming leads to collapse of the Gulf of Maine cod fishery. Science, 350, 809–12.Google Scholar
Petraitis, P. S. (1987). Factors organizing rocky intertidal communities of New England: herbivory and predation in sheltered bays. Journal of Experimental Marine Biology and Ecology, 109, 117–36.Google Scholar
Petraitis, P. S. (1998). How Can We Compare the Importance of Ecological Processes If We Never Ask, “Compared to What?” In Resetarits, W. and Bernardo, J., eds. Experimental Ecology, Issues and Perspectives. Oxford University Press, Oxford, pp. 183–201.Google Scholar
Petraitis, P. S. (2013). Multiple Stable States in Natural Ecosystems. Oxford University Press, Oxford.Google Scholar
Petraitis, P. S. and Dudgeon, S. R. (1999). Experimental evidence for the origin of alternative communities on rocky intertidal shores. Oikos, 84, 239–45.Google Scholar
Petraitis, P. S. and Dudgeon, S. R. (2004). Do alternate stable community states exist in the Gulf of Maine rocky intertidal zone? Comment. Ecology, 85, 1160–5.CrossRefGoogle Scholar
Petraitis, P. S. and Dudgeon, S. R. (2005). Divergent succession and implications for alternative states on rocky intertidal shores. Journal of Experimental Marine Biology and Ecology, 326, 14–26.Google Scholar
Petraitis, P. S. and Dudgeon, S. R. (2015). Variation in recruitment and the establishment of alternative stable states. Ecology, 96, 3186–96.Google Scholar
Petraitis, P. S. and Latham, R. E. (1999). The importance of scale in testing the origins of alternative community states. Ecology, 80, 429–42.Google Scholar
Petraitis, P. S. and Vidargas, N. (2006). Marine intertidal organisms found in experimental clearings on sheltered shores in the Gulf of Maine, USA (Ecological Archives E087–047). Ecology, 87, 795.Google Scholar
Petraitis, P. S., Latham, R. E. and Niesenbaum, R. A. (1989). The maintenance of species diversity by disturbance. Quarterly Reviews in Biology, 64, 393–418.Google Scholar
Petraitis, P. S., Liu, H. and Rhile, E. C. (2008). Densities and cover data for intertidal organisms in the Gulf of Maine, USA, from 2003 to 2007. Ecology, 89, 588.Google Scholar
Petraitis, P. S., Methratta, E. T., Rhile, E. C., Vidargas, N. A. and Dudgeon, S. R. (2009a). Experimental confirmation of multiple community states in a marine ecosystem. Oecologia, 161, 139–48.Google Scholar
Petraitis, P. S., Liu, H. and Rhile, E. C. (2009b). Barnacle, fucoid, and mussel recruitment in the Gulf of Maine, USA, from 1997 to 2007. Ecology, 90, 571.Google Scholar
Polis, G. A., Anderson, W. B. and Holt, R. D. (1997). Toward an integration of landscape and food web ecology: The dynamics of spatially subsidized food webs. Annual Review of Ecology and Systematics, 28, 289–316.Google Scholar
Rahmstorf, S. and Coumou, D. (2011). Increase of extreme events in a warming world. Proceedings of the National Academy of Sciences USA, 108, 17905–9.Google Scholar
Reid, D. G. (1996). Systematics and Evolution of Littorina. The Ray Society, Andover.Google ScholarPubMed
Roman, J. (2006). Diluting the founder effect: cryptic invasions expand a marine invader’s range. Proceedings of the Royal Society of London B, 273, 2453–9.Google Scholar
Rooney, N. and McCann, K. S. (2012). Integrating food web diversity, structure and stability. Trends in Ecology and Evolution, 27, 40–6.Google Scholar
Roughgarden, J., Gaines, S. D. and Possingham, H. (1988). Recruitment dynamics in complex life cycles. Science, 241, 1460–6.Google Scholar
Ruel, J. J. and Ayres, M. P. (1999). Jensen’s inequality predicts effects of environmental variation. Trends in Ecology and Evolution, 14 (9), 361–6.Google Scholar
Say, T. (1817). An account of the Crustacea of the United States. Journal of the Academy of Natural Sciences of Philadelphia, 1, 57–63.Google Scholar
Seeley, R. H. (1986). Intense natural selection caused a rapid morphological transition in a living marine snail. Proceedings of the National Academy of Sciences USA, 83, 6897–901.Google Scholar
Sephton, D., Vercaemer, B., Nicolas, J. M. and Keays, J. (2011). Monitoring for invasive tunicates in Nova Scotia, Canada (2006–2009). Aquatic Invasions, 6 (4), 391–403.Google Scholar
Silliman, B., McCoy, M. W., Trussell, G. C. et al. (2013). Non-linear interactions between consumers and flow determine the probability of plant community dominance on Maine rocky shores. PLoS ONE, 8 (8), e67625.Google Scholar
Sorte, C. J. B., Davison, V. E., Franklin, M. C. et al. (2017). Long-term declines in an intertidal foundation species parallel shifts in community composition. Global Change Biology, 23 (1), 341–52.Google Scholar
Spiess, A. E. and Lewis, R. A. (2001). The Turner farm fauna: 5000 years of hunting and fishing in Penobscot Bay, Maine. Occasional Publications in Maine Archaeology, 11, 1–177.Google Scholar
Stachowicz, J. J., Whitlach, R. B. and Osman, R. W. (1999). Species diversity and invasion resistance in a marine ecosystem. Science, 286, 1577–9.Google Scholar
Stachowicz, J. J., Terwin, J. R., Whitlatch, R. B. and Osman, R. W. (2002). Linking climate change and biological invasions: ocean warming facilitates nonindigenous species invasions. Proceedings of the National Academy of Sciences USA, 99, 15497–500.Google Scholar
Steneck, R. S. (1997). Fisheries-Induced Biological Changes to the Structure and Function of the Gulf of Maine Ecosystem. Plenary Paper. In Wallace, G. T and Braasch, E. F, eds. Proceedings of the Gulf of Maine Ecosystem Dynamics Scientific Symposium and Workshop, Report 91-1 – Regional Association for Research in the Gulf of Maine. RARGOM, Hanover, NH, pp. 151–65.Google Scholar
Steneck, R. S. and Carlton, J. T. (2001). Human Alterations of Marine Communities: Students Beware! In Bertness, M. D., Gaines, S. D. and Hay, M. E., eds. Marine Community Ecology. Sinauer Publishers, Sunderland, MA, pp. 445–68.Google Scholar
Steneck, R. S., Hughes, T. P., Cinner, J. E. et al. (2011). Creation of a gilded trap by the high economic value of the Maine lobster fishery. Conservation Biology, 25 (5), 904–12.Google Scholar
Stephenson, T. A. and Stephenson, A. (1972). Life between Tidemarks on Rocky Shores. Freeman Publishers, San Francisco.Google Scholar
Stephenson, E. H., Steneck, R. S. and Seeley, R. H. (2009). Possible temperature limits to range expansion of non-native Asian shore crabs in Maine. Journal of Experimental Marine Biology and Ecology, 375, 21–31.Google Scholar
Thompson, R. M., Beardall, J., Beringer, J., Grace, M. and Sardina, P. (2013) Means and extremes: building variability into community-level climate change experiments. Ecology Letters, 16, 799–806.Google Scholar
Thomsen, J., Casties, I., Pansch, C., Körtzinger, A. and Melzner, F. (2013). Food availability outweighs ocean acidification effects in juvenile Mytilus edulis: laboratory and field experiments. Global Change Biology, 19, 1017–27.Google Scholar
Thornber, C. S., Rinehart, S., Guidone, M. et al. (2013). Ecological dynamics of Ulva macroalgal blooms. Phycologia, 52 (4), S111.Google Scholar
Tilman, D. (1982). Resource Competition and Community Structure. Princeton University Press, Princeton, NJ.Google Scholar
Trussell, G. C. (1996). Phenotypic plasticity in an intertidal snail: the effects of a common crab predator. Evolution, 50, 448–54.Google Scholar
Trussell, G. C. (2000). Predator-induced plasticity and morphological trade-offs in latitudinally separated populations of Littorina obtusata. Evolutionary Ecology Research, 2, 803–22.Google Scholar
Trussell, G. C. and Nicklin, M. O. (2002). Cue sensitivity, inducible defence, and trade-offs: the influence of contrasting invasion histories between a crab predator and a marine snail. Ecology, 83, 1635–47.Google Scholar
Trussell, G. C. and Smith, L. D. (2000). Induced defences in response to an invading crab predator: an explanation of historical and geographic phenotypic change. Proceedings of the National Academy of Sciences USA, 97, 2123–7.Google Scholar
Trussell, G. C., Ewanchuk, P. J. and Bertness, M. D. (2003). Trait-mediated effects in rocky intertidal food chains: predator risk cues alter prey feeding rates. Ecology, 84 (3), 629–40.Google Scholar
Trussell, G. C., Ewanchuk, P. J., Bertness, M. D. and Silliman, B. R. (2004). Trophic cascades in rocky shore tidepools: distinguishing lethal and nonlethal effects. Oecologia, 139, 427–32.Google Scholar
Trussell, G. C., Ewanchuk, P. J. and Matassa, C. M. (2006). The fear of being eaten reduces energy transfer in a simple food chain. Ecology, 87 (12), 2979–84.Google Scholar
Ugarte, R. A., Critchley, A., Serdynska, A. R. and Deveau, J. P. (2007) Changes in composition of rockweed (Ascophyllum nodosum) beds due to possible recent increase in sea temperature in Eastern Canada. Journal of Applied Phycology, 21, 591–8.Google Scholar
Underwood, A. J. and Fairweather, P. G. (1989). Supply-side ecology and benthic marine assemblages. Trends in Ecology and Evolution, 4, 16–20.Google Scholar
Vadas, R. L. Sr. (1992). Littorinid Grazing and Algal Patch Dynamics. In Grahame, J., Mill, P. J. and Reid, D. G., eds. Proceedings of the Third International Symposium on Littorinid Biology. The Malacological Society of London, London.Google Scholar
Vadas, R. L. Sr. and Elner, R. W. (1992). Plant–Animal Interactions in the Northwest Atlantic. In John, D. M., Hawkins, S. J. and Price, J. H., eds. Plant–Animal Interactions in the Marine Benthos. The Systematics Association Special Volume No. 46, Clarendon Press, Oxford, pp. 33–60.Google Scholar
Vadas, R. L. and Manzer, F. (1971). The Use of Aerial Colour Photography for Studies on Rocky Intertidal Benthic Marine Algae. In Anson, A., ed. Proceedings of the Third Biennial Workshop on Aerial Colour Photography in the Plant Sciences and Related Fields. American Society of Photogrammetry, Bethesda, MA, pp. 255–66.Google Scholar
Vadas, R. L. Sr., Wright, W. A. and Beal, B. F. (2004) Biomass and productivity of intertidal rockweeds (Ascophyllum nodosum LeJolis) in Cobscook Bay. Northeastern Naturalist, 11 (Special Issue), 123–42.Google Scholar
Valiela, I., McClellan, J., Hauxwell, J., Behr, P. J., Hersh, D. and Foreman, K. (1997). Macroalgal blooms in shallow estuaries: Controls and ecophysiological and ecosystem consequences. Limnology and Oceanography, 42, 1105–18.Google Scholar
Vasseur, D. A., DeLong, J. P., Gilbert, B. et al. (2014). Increased temperature variation poses a greater risk to species than climate warming. Proceedings of the Royal Society of London B, 281, 20132612.Google Scholar
Vazquez, K. E. (2015). Phenotypic variation in the dogwhelk, Nucella lapillus: an integration of ecology, karyotype, and phenotypic plasticity. PhD, University of Pennsylvania.Google Scholar
Vermeij, G. J. (1982). Phenotypic evolution in a poorly dispersing snail after arrival of a predator. Nature, 299, 349–50.Google Scholar
Vermeij, G. J. (1991). Anatomy of an invasion: the trans-Arctic interchange. Paleobiology, 17, 281–307.Google Scholar
Vermeij, G. J. (2001). Community Assembly in the Sea: Geologic History of the Living Shore Biota. In Bertness, M. D., Gaines, S. D. and Hay, M. E., eds, Marine Community Ecology. Sinauer Publishers, Sunderland, MA, pp. 39–60.Google Scholar
Wagner, A. (2017). The White-Knight Hypothesis, or does the environment limit innovations? Trends in Ecology and Evolution, 32 (2), 131–40.Google Scholar
Wang, Z. A., Wanninkhof, R., Cai, W.-J. et al. (2013). The marine inorganic carbon system along the Gulf of Mexico and Atlantic coasts of the United States: Insights from a transregional coastal carbon study. Limnology and Oceanography, 58 (1), 325–42.Google Scholar
Wares, J. P. and Cunningham, C. W. (2001). Phylogeography and historical ecology of the North Atlantic intertidal. Evolution, 55 (12), 2455–69.Google Scholar
Wernberg, T., Bennett, S., Babcock, R. C. et al. (2016). Climate-driven regime shift of a temperate marine ecosystem. Science, 353, 169–72.Google Scholar
Wethey, D. S. (1985). Catastrophe, extinction, and species diversity: a rocky intertidal example. Ecology, 66, 445–56.Google Scholar
Wethey, D. S. (2002). Biogeography, competition, and microclimate: the barnacle Chthamalus fragilis in New England. Integrative and Comparative Biology, 42, 872–80.Google Scholar
Witman, J. D., Etter, R. J. and Smith, F. (2004). The relationship between regional and local species diversity in marine benthic communities: a global perspective. Proceedings of the Natural Academy of Sciences USA, 101, 15664–9.Google Scholar
Wootton, J. T., Pfister, C. A. and Forester, J. D. (2008). Dynamic patterns and ecological impacts of declining ocean pH in a high-resolution multi-year dataset. Proceedings of the National Academy of Sciences USA, 105, 18848–53.Google Scholar
Worm, B. and Lotze, H. K. (2006). Effects of eutrophication, grazing, and algal blooms on rocky shores. Limnology and Oceanography, 51 (1, part 2), 569–79.Google Scholar
Worm, B., Lotze, H. K., Boström, C., Engkvist, R., Labanauskas, V. and Sommer, U. (1999). Marine diversity shift linked to interactions among grazers, nutrients and dormant propagules. Marine Ecology Progress Series, 185, 309–14.Google Scholar
Worm, B., Lotze, H. K. and Sommer, U. (2001). Algal propagule banks modify competition, consumer and resource control on Baltic rocky shore. Oecologia, 128, 281–93.Google Scholar
Worm, B., Lotze, H. K., Hillebrand, H. and Sommer, U. (2002). Consumer versus resource control of species diversity and ecosystem functioning. Nature, 417, 848–51.Google Scholar
Young, A. M., Torres, C., Mack, J. E. and Cunningham, C. W. (2002). Morphological and genetic evidence for vicariance and refugium in Atlantic and Gulf of Mexico populations of the hermit crab, Pagurus longicarpus. Marine Biology, 140 (5), 1059–66.Google Scholar
Zhao, X. G., Guo, C., Han, Y. et al. (2017). Ocean acidification decreases mussel byssal attachment strength and induces molecular byssal responses. Marine Ecology Progress Series, 565, 67–77.Google Scholar

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