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Chapter 15 - Biogeographic Comparisons of Pattern and Process on Intertidal Rocky Reefs of New Zealand and South-Eastern Australia

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

The rocky shores of New Zealand (NZ) and Australia provide many interesting comparisons in their intertidal species and structuring processes. Both countries are in the biogeographic realm of temperate Australasia and share many common species and closely related taxa. Here we review similarities and contrasts in communities and structuring processes, especially involving grazing invertebrates and macroalgae. We consider the similarity of the structure of intertidal shores of NZ and south-eastern Australia, a suite of important trophic interactions within and between regions, the utility of local-scale experiments in understanding large-scale processes and how we might better plan for and manage our coasts. The major comparisons are between warm-temperate areas of northern NZ and New South Wales, and the cooler areas of southern NZ and south-eastern Australia. In the quest for ‘ecosystem’-level understanding, which perforce involves large-scale events, there is an increasing tendency to minimise or ignore the hard-won insights gained from well-structured experiments across multiple sites. Because all large-scale effects must be manifested at local sites, it is incumbent on us to determine what scales up or down, and the caveats that make comparisons across biogeographic regions challenging. Here, we discuss these issues using austral shores as models.

Type
Chapter
Information
Interactions in the Marine Benthos
Global Patterns and Processes
, pp. 391 - 413
Publisher: Cambridge University Press
Print publication year: 2019

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References

Alestra, T. and Schiel, D. (2015). Impacts of local and global stressors in intertidal habitats: influence of altered nutrient, sediment and temperature levels on the early life history of three habitat-forming macroalgae. Journal of Experimental Marine Biology and Ecology, 468, 2936.Google Scholar
Alestra, T., Tait, L. and Schiel, D. (2014). Effects of algal turfs and sediment accumulation on replenishment and primary productivity of fucoid assemblages. Marine Ecology Progress Series, 511, 5970.CrossRefGoogle Scholar
Bennett, I. and Pope, E. C. (1953). Intertidal zonation of the exposed rocky shores of Victoria, together with a reassignment of the biogeographical provinces of temperate Australian shores. Australian Journal of Marine and Freshwater Research, 4, 105–59.Google Scholar
Bennett, I. and Pope, E. C. (1960). Intertidal zonation of the exposed rocky shores of Tasmania and its relationship with the rest of Australia. Australian Journal of Marine and Freshwater Research, 11, 182221.Google Scholar
Blanchette, C. A., Wieters, E. A., Broitman, B. R., Kinlan, B. P. and Schiel, D. R. (2009). Trophic structure and diversity in rocky intertidal upwelling ecosystems: a comparison of community patterns across California, Chile, South Africa and New Zealand. Progress in Oceanography, 83, 107–16.Google Scholar
Bulleri, F., Benedetti-Cecchi, L., Cusson, M. et al. (2012). Temporal stability of European rocky shore assemblages: variation across a latitudinal gradient and the role of habitat-formers. Oikos, 121, 1801–9.Google Scholar
Chapman, M. G. (1994). Small-scale patterns of distribution and size-structure of the intertidal littorinid Littorina unifasciata (Gastropoda: Littorinidae) in New South Wales. Australian Journal of Marine and Freshwater Research, 45, 635–52.Google Scholar
Chapman, M. G. and Underwood, A. J. (1998). Inconsistency and variation in the development of rocky intertidal algal assemblages. Journal of Experimental Marine Biology and Ecology, 224, 265–89.Google Scholar
Cole, V. J. and McQuaid, C. D. (2011). Broad-scale spatial factors outweigh the influence of habitat structure on the fauna associated with a bioengineer. Marine Ecology Progress Series, 442, 101–9.Google Scholar
Coleman, R. A., Underwood, A. J., BenedettiCecchi, L. et al. (2006). A continental scale evaluation of the role of limpet grazing on rocky shores. Oecologia, 147, 556–64.CrossRefGoogle ScholarPubMed
Connor, E. F. and Simberloff, D. (1978). Species number and compositional similarity of the Galapagos flora and avifauna. Ecological Monographs, 48, 219–48.CrossRefGoogle Scholar
Creese, R. G. (1988). Ecology of molluscan grazers and their interactions with marine algae in north-eastern New Zealand. New Zealand Journal of Marine and Freshwater Research, 22, 427–44.Google Scholar
Creese, R. and Underwood, A. (1982). Analysis of inter-and intra-specific competition amongst intertidal limpets with different methods of feeding. Oecologia, 53, 337–46.Google Scholar
Crowe, T. P., Cusson, M., Bulleri, F. et al. (2013). Large-scale variation in combined impacts in canopy-loss and disturbance on community structure and ecosystem functioning. PLoS ONE, 8, e66238.CrossRefGoogle ScholarPubMed
Dakin, W. J. (1953). Australian Sea Shores. Angus & Robertson, Sydney.Google Scholar
Dugan, J. E., Airoldi, L., Chapman, M. G., Walker, S. J. and Schlacher, T. (2011). Estuarine and Coastal Structures: Environmental Effects, a Focus on Shore and Nearshore Structures. In Wolanski, E. and MccLusky, D. S., eds. Treatise on Estuarine and Coastal Science. Academic Press, Waltham, pp. 1741.Google Scholar
Dunmore, R. and Schiel, D. (2003). Demography, competitive interactions and grazing effects of intertidal limpets in southern New Zealand. Journal of Experimental Marine Biology and Ecology, 288, 1738.CrossRefGoogle Scholar
EEA. (2005). The European Environment, State and Outlook. European Environment Agency, Copenhagen.Google Scholar
Foley, M. M., Armsby, M. H., Prahler, E. E. et al. (2013). Improving ocean management through the use of ecological principles and integrated ecosystem assessments. Bioscience, 63, 619–31.Google Scholar
Foster, M. S. (1990). Organization of macroalgal assemblages in the Northeast Pacific: the assumption of homogeneity and the illusion of generality. Hydrobiology, 192, 2133.Google Scholar
Foster, M. S. and Schiel, D. R. (2010). Loss of predators and the collapse of southern California kelp forests (?): alternatives, explanations and generalizations. Journal of Experimental Marine Biology and Ecology, 393, 5970.Google Scholar
Gaines, S. D. and Lubchenco, J. (1982). A unified approach to marine plant-herbivore interactions. 2. Biogeography. Annual Review of Ecology and Systematics, 13, 111–38.Google Scholar
Gaston, K. J. (1994). Rarity. Chapman & Hall, London.CrossRefGoogle Scholar
Gray, J. S. (2001). Marine diversity: the paradigms in patterns of species richness examined. Scientia Marina, 65, 4156.Google Scholar
Guerry, A.D, Menge, B.A. and Dunmore, R.A. (2009). Effects of consumers and enrichment on abundance and diversity of benthic algae in a rocky intertidal community. Journal of Experimental Marine Biology and Ecology, 369, 155–64.Google Scholar
Hawkins, S. J. and Hartnoll, R. G. (1983). Grazing of intertidal algae by marine invertebrates. Annual Review of Oceanography and Marine Biology, 21, 195282.Google Scholar
Helmuth, B., Mieszkowska, N., Moore, P. and Hawkins, S. J. (2006). Living on the edge of two changing worlds: forecasting the responses of rocky intertidal ecosystems to climate change. Annual Review of Ecology, Evolution, and Systematics, 37, 373404.Google Scholar
Hidas, E. Z., Ayre, D. J. and Minchenton, T. E. (2010). Patterns of demography for rocky-shore, intertidal invertebrates approaching their geographica range limits: tests of the abundant-centre hypothesis in south-eastern Australia. Marine and Freshwater Research, 61, 1243–51.Google Scholar
Hobbs, R. J., Higgs, E. and Harris, J. A. (2009). Novel ecosystems: implications for conservation and restoration. Trends in Ecology and Evolution, 24,599605.Google Scholar
Hurlbert, S. J. (1984). Pseudoreplication and the design of ecological field experiments. Ecological Monographs, 54, 187211.Google 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, S323.CrossRefGoogle ScholarPubMed
Johnson, C. R., Banks, S. C., Barrett, N. S. et al. (2011). Climate change cascades: shifts in oceanography, species’ ranges and subtidal marine community dynamics in eastern Tasmania. Journal of Experimental Marine Biology and Ecology, 400, 1732.Google Scholar
Keough, M. J. and Quinn, G. (1998). Effects of periodic disturbances from trampling onrocky intertidal algal beds. Ecological Applications, 8, 141–61.Google Scholar
Knox, G. A. (1963). The biogeography and intertidal ecology the Australasian coasts. Oceanography and Marine Biology, 1, 341404.Google Scholar
Knox, G. A. (1980). Plate tectonics and the evolution of intertidal and shallow-water benthic distribution patterns of the southwest Pacific. Palaeogeography Palaeoclimatology Palaeoecology, 31, 267–97.Google Scholar
Kortsch, S., Primicerio, R., Fossheim, M., Dolgov, A. V. and Aschan, M. (2015). Climate change alters the structure of arctic marine food webs due to poleward shifts of boreal generalists. Proceedings of the Royal Society B-Biological Sciences, 282, 31–9.Google Scholar
Lathlean, J. A., Ayre, D. J. and Minchenton, D. E. (2010). Supply-side biogeography: geographic patterns of settlement and early mortality for a barnacle approaching its range limit. Marine Ecology Progress Series, 412, 141–50.CrossRefGoogle Scholar
Lathlean, J. A., McWilliam, R. A., Ayre, D. J. and Minchenton, T. E. (2015). Biogeographical patterns of rocky-shore community structure in south-east Australia: effects of oceanographic conditions and heat stress. Journal of Biogeography, 42, 1538–52.Google Scholar
Lilley, S. A. and Schiel, D. R. (2006). Community effects following the deletion of a habitat-forming alga from rocky marine shores. Oecologia, 148, 672–81.Google Scholar
Lubchenco, J. and Gaines, S. D. (1981). A unified approach to marine plant-herbivore interactions. I. Population and communities. Annual Review of Ecology and Systematics, 12, 405–37.Google Scholar
Lundquist, C. J., Fisher, K. T., Le Heron, R. et al. (2016). Science and societal partnerships to address cumulative impacts. Frontiers in Marine Science, 3, 2.Google Scholar
Martins, G. M., Jenkins, S. R., Ramírez, R., Tuya, F., Neto, A. I. and Arenas, F. (2014). Early patterns of recovery from disturbance in intertidal algal assemblages: consistency across regions within a marine province. Marine Ecology Progress Series, 517, 131–42.Google 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, 297330.Google Scholar
Menge, B.A. and Menge, D.N. (2013). Dynamics of coastal meta‐ecosystems: the intermittent upwelling hypothesis and a test in rocky intertidal regions. Ecological Monographs, 83, 283310.Google Scholar
Moore, L. B. (1949). The marine algal provinces of New Zealand. Transactions for the Royal Society of New Zealand, 77, 187–9.Google 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, 437–47.Google Scholar
Nelson, W. A., Dalen, J. and Neill, K. F. (2013). Insights from natural history collections: analysing the New Zealand macroalgal flora using herbarium data. PhytoKeys, 30, 121.CrossRefGoogle Scholar
O’Gower, A. K. and Meyer, G. R. (1971). The ecology of six species of littoral gastropod molluscs. 3. Diurnal and seasonal variations in densities and patterns of distribution in three environments. Australian Journal of Marine and Freshwater Research, 22, 3540.Google Scholar
Olson, D. M., Dinerstein, E., Wikramanayake, E. D. et al. (2001). Terrestrial ecoregions of the world: a new map of life on Earth a new global map of terrestrial ecoregions provides an innovative tool for conserving biodiversity. Bioscience, 51, 933–8.Google Scholar
Povey, A. and Keough, M. J. (1991). Effects of trampling on plant and animal populations on rocky shores. Oikos, 61, 355–68.Google Scholar
Quinn, G. P. and Keough, M. J. (2002). Experimental Design and Data Analysis for Biologists. Cambridge University Press, Cambridge.Google Scholar
Resetarits, W. J. and Bernardo, J. (1998). Experimental Ecology: Issues and Perspectives. Oxford University Press, Oxford.Google Scholar
Rilov, G. and Schiel, D. R. (2006a). Seascape-dependent subtidal-intertidal trophic linkages. Ecology, 87, 731–44.CrossRefGoogle ScholarPubMed
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.Google Scholar
Rilov, G. and Schiel, D. R. (2011). Community regulation: the relative importance of recruitment and predation intensity of an intertidal community dominant in a seascape context. PLoS ONE, 6, e23958.Google Scholar
Romero, S., Le Gendreb, R., Garniera, J. et al. (2016). Long-term water quality in the lower Seine: lessons learned over 4 decades of monitoring. Environmental Science & Policy, 58, 141–54.Google Scholar
Scheiner, S. M. (2003). Six types of species-area curves. Global Ecology and Biogeography, 12, 441–7.CrossRefGoogle Scholar
Schiel, D. R. (2006). Rivets or bolts? When single species count in the function of temperate rocky reef communities. Journal of Experimental Marine Biology and Ecology, 338, 233–52.Google Scholar
Schiel, D. R. (2011). Biogeographic patterns and long-term changes on New Zealand coastal reefs: non-trophic cascades from diffuse and local impacts. Journal of Experimental Marine Biology and Ecology, 400, 3351.Google Scholar
Schiel, D. R. (2013). The other 93%: trophic cascades, stressors and managing coastlines in non-marine protected areas. New Zealand Journal of Marine and Freshwater Research, 47, 374–91.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, 5764.CrossRefGoogle Scholar
Schiel, D. R. and Lilley, S. A. (2007). Gradients of disturbance to an algal canopy and the modification of an intertidal community. Marine Ecology Progress Series, 339, 111.CrossRefGoogle Scholar
Schiel, D. R. and Lilley, S. A. (2011). Impacts and negative feedbacks in community recovery over eight years following removal of habitat-forming macroalgae. Journal of Experimental Marine Biology and Ecology, 407, 108–15.Google Scholar
Schiel, D. R., Lilley, S. A., South, P. M. and Coggins, J. H. (2016). Decadal changes in sea surface temperature, wave forces and intertidal structure in New Zealand. Marine Ecology Progress Series, 548, 7795.Google Scholar
Schiel, D. R. and Taylor, D. I. (1999). Effects of trampling on a rocky intertidal algal assemblage in southern New Zealand. Journal of Experimental Marine Biology and Ecology, 235, 213–35.Google Scholar
Schiel, D. R., Wood, S. A., Dunmore, R. A. and Taylor, D. I. (2006). Sediment on rocky intertidal reefs: effects on early post-settlement stages of habitat-forming seaweeds. Journal of Experimental Marine Biology and Ecology, 331(2), 158–72.CrossRefGoogle Scholar
Seastedt, T. R., Hobbs, R. J. and Suding, K. N. (2008). Management of novel ecosystems: are novel approaches required? Frontiers in Ecology and the Environment, 6, 547–53.Google Scholar
Simberloff, D. (1980). A Succession of Paradigms in Ecology: Essentialism, Materialism and Probabilism. In Saarinen, E., ed. Conceptual Issues in Ecology. Reidel, Dordrecht, pp. 6399.Google Scholar
Spalding, M. D., Fox, H. E., Halpern, B. S. et al. (2007). Marine ecoregions of the world: a bioregionalization of coastal and shelf areas. Bioscience, 57, 573–83.Google Scholar
Tait, L. W. and Schiel, D. R. (2011). Legacy effects of canopy disturbance on ecosystem functioning in macroalgal assemblages. PLoS ONE, 6, e26986.Google Scholar
Taylor, D., Delaux, S., Stevens, C., Nokes, R. and Schiel, D. (2010). Settlement rates of macroalgal algal propagules: cross‐species comparisons in a turbulent environment. Limnology and Oceanography, 55, 6676.Google Scholar
Taylor, D. I. and Schiel, D. R. (2010). Algal populations controlled by fish herbivory across a wave exposure gradient on southern temperate shores. Ecology, 91, 201–11.Google Scholar
Thompson, R., Crowe, T. and Hawkins, S. (2002). Rocky intertidal communities: past environmental changes, present status and predictions for the next 25 years. Environmental Conservation, 29, 168–91.Google Scholar
Underwood, A. J. (1980). The effects of grazing by gastropods and physical factors on the upper limits of distribution of intertidal macroalgae. Oecologia, 46, 201–13.CrossRefGoogle ScholarPubMed
Underwood, A. J. (1984a). Vertical and seasonal patterns in competition for microalgae between intertidal gastropods. Oecologia, 64, 211–22.Google Scholar
Underwood, A. J. (1984b). 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, 199220.Google Scholar
Underwood, A. J. (1986). The Analysis of Competition by Field Experiments. In Kikkawa, J. and Anderson, D. J., eds. Community Ecology: Pattern and Process. Blackwells, Melbourne, pp. 240–68.Google Scholar
Underwood, A. J. (1990). Experiments in ecology and management: their logics, functions and interpretations. Australian Journal of Ecology, 15, 365–89.Google 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, 291306.Google Scholar
Underwood, A. J. (1999a). Physical disturbances and their direct effects on an indirect effect: responses of an intertidal assemblage to a severe storm. Journal of Experimental Marine Biology and Ecology, 232, 125–40.Google Scholar
Underwood, A. J. (1999b). History and Recruitment in the Structure of Intertidal Assemblages on Rocky Shores: An Introduction to Problems for Interpretation of Natural Change. In Whitfield, M., Matthews, J. and Reynolds, C., eds. Aquatic Life Cycle Strategies. Institute of Biology, London, pp. 7996.Google Scholar
Underwood, A. J., Cole, V. J., Palomo, M. G. and Chapman, M. G. (2008). Numbers and density of species as measures of biodiversity on rocky shores along the coast of New South Wales. Journal of Experimental Marine Biology and Ecology, 366, 175–83.Google Scholar
Underwood, A. J. and Denley, E. J. (1984). Paradigms, Explanations and Generalizations in Models for the Structure of Intertidal Communities on Rocky Shores. In Strong, D. R., Simberloff, D., Abele, L. G. and Thistle, A., eds. Ecological Communities: Conceptual Issues and the Evidence. Princeton University Press, Princeton, NJ, pp. 151–80.Google Scholar
Underwood, A. J., Denley, E. J. and Moran, M. J. (1983). Experimental analyses of the structure and dynamics of mid-shore rocky intertidal communities in New South Wales. Oecologia, 56, 202–19.Google Scholar
Underwood, A. J. and Jernakoff, P. (1981). Effects of interactions between algae and grazing gastropods in the structure of a low-shore algal community. Oecologia, 48, 221–33.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, 7196.Google Scholar
Underwood, A. J. and Murphy, R. J. (2008). Unexpected patterns in facilitatory grazing revealed by quantitative imaging. Marine Ecology Progress Series, 358, 8594.Google Scholar
Underwood, A. J. and Petraitis, P. S. (1993). Structure of Intertidal Assemblages in Different Locations: How Can Local Processes Be Compared? In Ricklefs, R. E. and Schluter, D., eds. Species Diversity in Ecological Communities: Historical and Geographical Perspectives. University of Chicago Press, Chicago, pp. 3851.Google Scholar
Villarino, E., Chust, G., Licandro, P. et al. (2015). Modelling the future biogeography of North Atlantic zooplankton communities in response to climate change. Marine Ecology Progress Series, 531, 121–42.CrossRefGoogle Scholar
Walker, N. A. (1998). Grazing in the intertidal zone: effects of the herbivorous Turbo smaragdus on macroalgal assemblages. Masters thesis, University of Canterbury, Canterbury.Google Scholar
Waters, J. M., Wernberg, T., Connell, S. D. et al. (2010). Australia’s marine biogeography revisited: back to the future? Austral Ecology, 35, 988–92.Google Scholar
Wiens, J. A. (1989). Spatial scaling in ecology. Functional Ecology, 3, 385–97.Google Scholar
Wieters, E. A., McQuaid, C. D., Palomo, M. G., Pappalardo, P. and Navarrete, S. (2012). Biogeographcal boundaries, functional group structure and diversity of rocky shore communities along the Argentinian coast. PLoS ONE, 7, e49725.CrossRefGoogle Scholar
Womersley, H. B. S. and Edmonds, S. J. (1958). A general account of the intertidal ecology of South Australian coasts. Australian Journal of Marine and Freshwater Reserarch, 9, 217–60.Google Scholar

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