Home Persistence of sea urchin (Heliocidaris erythrogramma) barrens on the east coast of Tasmania: inhibition of macroalgal recovery in the absence of high densities of sea urchins
Article
Licensed
Unlicensed Requires Authentication

Persistence of sea urchin (Heliocidaris erythrogramma) barrens on the east coast of Tasmania: inhibition of macroalgal recovery in the absence of high densities of sea urchins

  • Joseph P. Valentine and Craig R. Johnson
Published/Copyright: July 5, 2005
Botanica Marina
From the journal Volume 48 Issue 2

Abstract

Sea urchin barrens occur commonly in temperate regions throughout the world and have significant implications for ecological processes on subtidal rocky reefs because they constitute areas of low productivity and diversity compared with habitats dominated by macroalgae. On the east coast of Tasmania, the occurrence of sea urchin (Heliocidaris erythrogramma) barrens in sheltered bays has additional implications in that they represent an important habitat of the introduced kelp Undaria pinnatifida. Identifying the factors responsible for ongoing maintenance of the barren habitat is essential in defining management options to promote recovery of native canopy-forming species. We used transplant experiments to investigate whether inhibition of recovery of native canopy-forming algae can occur in the absence of intense sea urchin grazing. High densities of native canopy-forming species successfully colonised paving blocks deployed in a dense algal bed adjacent to a sea urchin barren. Transplanting these paving blocks to plots on the barren from which sea urchins were removed resulted in >80% mortality of recruits after three months, and 100% mortality after seven months. The decline in macroalgal recruits on paving blocks transplanted to the urchin barren was associated with an increase in the cover and depth of sediment. A persistent cover of sediment also developed on paving blocks deployed on the urchin barren, where no native canopy-forming algal recruits were observed. While sea urchins are undoubtedly important in creating urchin barrens, our results suggest that other mechanisms can influence recovery of native canopy species. In sheltered and semi-exposed bays on the east coast of Tasmania, sedimentation appears to play a critical role in inhibiting early developmental stages of native macroalgae, thereby contributing to a positive feedback that acts to maintain the barren habitat.

:

Corresponding author

References

Agatsuma, Y., K. Matsuyama, A. Nakata, T. Kawai and N. Nishikawa. 1997. Marine algal succession on coralline flats after removal of sea urchins in Suttsu Bay on the Japan Sea coast of Hokkaido, Japan. Nippon. Suisan. Gakk.63: 672–680.Search in Google Scholar

Agatsuma, Y., A. Nakata, and K. Matsuyama. 2000. Seasonal foraging activity of the sea urchin Stronglyocentrotus nudus on coralline flats in Oshoro Bay in south-western Hokkaido, Japan. Fish. Sci.66: 198–203.Search in Google Scholar

Airoldi, L. 2003. The effects of sedimentation on rocky coast assemblages. Oceanogr. Mar. Biol. Annu. Rev.41: 161–236.Search in Google Scholar

Airoldi, L. and M. Virgilio. 1998. Responses of turf-forming algae to spatial variations in the deposition of sediments. Mar. Ecol. Prog. Ser.165: 271–282.10.3354/meps165271Search in Google Scholar

Ambrose, R.F. and B.V. Nelson. 1982. Inhibition of giant kelp recruitment by an introduced brown alga. Bot. Mar.15: 265–267.10.1515/botm.1982.25.6.265Search in Google Scholar

Anderson, E.K. and W.J. North. 1966. In situ studies of spore production and dispersal in the giant kelp, Macrocystis. Proc. Int. Seaweed. Symp.5: 73–86.10.1016/B978-0-08-011841-3.50011-2Search in Google Scholar

Andrew, N.L. and A.J. Underwood. 1993. Density-dependent foraging in the sea urchin Centrostephanus rodgersii on shallow subtidal reefs in New South Wales, Australia. Mar. Ecol. Prog. Ser.99: 89–98.10.3354/meps099089Search in Google Scholar

Andrew, N.L. and R.M. Viejo. 1998. Ecological limits to the invasion of Sargassum muticum in northern Spain. Aquat. Bot.60: 251–263.10.1016/S0304-3770(97)00088-0Search in Google Scholar

Arakawa, H. and K. Matsuike. 1992. Influence on insertion of zoospores, germination, survival, and maturation of gametophytes of brown algae exerted by sediments. Nippon. Suisan. Gakk.58: 619–625.Search in Google Scholar

Chapman, A.R.O. 1981. Stability of sea urchin dominated barren grounds following destructive grazing of kelp in St. Margaret's Bay, eastern Canada. Mar. Biol.62: 307–311.10.1007/BF00397697Search in Google Scholar

Chapman, A.R.O. and C.R. Johnson. 1990. Disturbance and organisation of macroalgal assemblages in the Northwest Atlantic. Hydrobiologia192: 77–121.10.1007/BF00006228Search in Google Scholar

Chapman, A.S. and F.L. Fletcher. 2002. Differential effects of sediments on survival and growth of Fucus serratus embryos (Fucales, Phaeophyceae) J. Phycol.38: 894–903.10.1046/j.1529-8817.2002.t01-1-02025.xSearch in Google Scholar

Choat, J.H. and D.R. Schiel. 1982. Patterns of distribution and abundance of large brown algae and invertebrate herbivores in subtidal regions of northern New Zealand. J. Exp. Mar. Biol. Ecol.60: 129–162.10.1016/0022-0981(82)90155-1Search in Google Scholar

Coelho, S.M., J.W. Rijstenbil and M.T. Brown. 2000. Impacts of anthropogenic stresses on the early development stages of seaweeds. J. Aquat. Ecosyst. Stress Recovery7: 317–333.10.1023/A:1009916129009Search in Google Scholar

Dayton, P.K. 1985. Ecology of kelp communities. Annu. Rev. Ecol. Syst.16: 215–245.10.1146/annurev.es.16.110185.001243Search in Google Scholar

Dayton, P.K., V. Currie, T. Gerrodette, B.D. Keller, R. Rosenthal, and D. Ven Tresca. 1984. Patch dynamics and stability of some Californian kelp communities. Ecol. Monogr.54: 253–289.10.2307/1942498Search in Google Scholar

Devinny, J.S. and I.A. Volse. 1978. The effects of sediments on the development of Macrocystis pyrifera gametophytes. Mar. Biol.48: 343–348.10.1007/BF00391638Search in Google Scholar

Draper, N. and H. Smith. 1981. Applied regression analysis. Wiley, New York.Search in Google Scholar

Duggins, D.O. 1980. Kelp beds and sea otters: an experimental approach. Ecology61: 447–453.10.2307/1937405Search in Google Scholar

Estes, J.A. and J.F. Palmisano. 1974. Sea otters: their role in structuring nearshore communities. Science185: 1058–1060.10.1126/science.185.4156.1058Search in Google Scholar PubMed

Fletcher, W.J. 1987. Interactions among subtidal Australian sea urchins, gastropods, and algae: effects of experimental removals. Ecol. Monogr.57: 89–109.Search in Google Scholar

Foster, M.S. 1975. Algal succession in a Macrocystis pyrifera forest. Mar. Biol.32: 313–329.10.1007/BF00388989Search in Google Scholar

Hagen, N.T. 1995. Recurrent destructive grazing of successionally immature kelp forests by green sea urchins in Vestfjorden, Northern Norway. Mar. Ecol. Prog. Ser.123: 95–106.10.3354/meps123095Search in Google Scholar

Hanelt, D. 1996. Photoinhibition of photosynthesis in marine macroalgae. Sci. Mar.60: 243–248.Search in Google Scholar

Hanelt, D., B. Mechersmann, C. Wiencke and W. Nultsch. 1997. Effects of high light stress on photosynthesis of polar macroalgae. Mar. Ecol. Prog. Ser.149: 255–266.10.3354/meps149255Search in Google Scholar

Himmelman, J.H., A. Cardinal and E. Bourget. 1983. Community development following removal of sea urchins. Stronglyocentrotus droebachiensis, from the rocky subtidal zone of the St. Lawrence estuary, eastern Canada. Oecologia59: 27–39.Search in Google Scholar

Johnson, C.R. and K.H. Mann. 1988. Diversity, patterns of adaptation and stability of Novia Scotian kelp beds. Ecol. Monogr.58: 129–154.Search in Google Scholar

Johnson, C.R. and K.H. Mann. 1993. Rapid succession in subtidal understorey seaweeds during recovery from overgrazing by sea urchins in eastern Canada. Bot. Mar.36: 63–77.10.1515/botm.1993.36.1.63Search in Google Scholar

Johnson, C.R., J.P. Valentine and H.G. Pederson. 2004. A most unusual barrens: complex interactions between lobsters, sea urchins and algae facilitates spread of an exotic kelp in eastern Tasmania. In: (T. Heinzeller, J.H. Nebelsick, eds) Proceedings of the International Echinoderm Conference, Munich, 6–10 October 2003, Rotterdam. Balkema, Leiden. pp. 213–220.Search in Google Scholar

Keats, D.W., G.R. South and D.H. Steele. 1990. Effects of experimental reduction in grazing by green sea urchins on a benthic macroalgal community in eastern Newfoundland. Mar. Ecol. Prog. Ser.68: 181–193.10.3354/meps068181Search in Google Scholar

Kennelly, S.J. 1987. Physical disturbances in an Australian kelp community. I. Temporal effects. Mar. Ecol. Prog. Ser.40: 145–153.10.3354/meps040145Search in Google Scholar

Kennelly, S.J. 1989. Effects of kelp canopies on understorey species due to shade and scour. Mar. Ecol. Prog. Ser.50: 215–224.10.3354/meps050215Search in Google Scholar

Kennelly, S.J. and A.J. Underwood. 1993. Geographic consistencies of effects of experimental physical disturbance on understorey species in sublittoral kelp forests in central New South Wales. J. Exp. Mar. Biol. Ecol.168: 35–58.10.1016/0022-0981(93)90115-5Search in Google Scholar

Lawrence, J.M. 1975. On the relationships between marine plants and sea urchins. Oceanogr. Mar. Biol. Annu. Rev.13: 213–286.Search in Google Scholar

Leinaas, H.P. and H. Christie. 1996. Effects of removing sea urchins (Stronglyocentrotus droebachiensis): stability of the barren state and succession of kelp forest recovery in the east Atlantic. Oecologia105: 524–536.10.1007/BF00330016Search in Google Scholar

Littler, M.M., Martz, D.R. and D.S. Littler. 1983. Effects of recurrent sand deposition on rocky intertidal organisms: importance of substrate heterogeneity in a fluctuating environment. Mar. Ecol. Prog. Ser.11: 129–139.10.3354/meps011129Search in Google Scholar

Melville, A.J. and S.D. Connell. 2001. Experimental effects of kelp canopies on subtidal coralline algae. Austral. Ecol.26: 102–108.10.1046/j.1442-9993.2001.01089.xSearch in Google Scholar

Renaud, P.E., S.R. Riggs, W.G. Ambrose, Jr., K. Schmid and S.W. Snyder. 1997. Biological-geological interactions: storm effects on macroalgal communities mediated by sediment characteristics and distribution. Cont. Shelf Res.17: 383–398.10.1016/0278-4343(96)00019-2Search in Google Scholar

Sanderson, J.C. 1990. A preliminary survey of the distribution of the introduced macroalga, Undaria pinnatifida (Harvey) Suringer on the East Coast of Tasmania, Australia. Bot. Mar.33: 153–157.10.1515/botm.1990.33.2.153Search in Google Scholar

Sanderson, J.C. 1997. Survey of Undaria pinnatifida in Tasmanian coastal waters, January-February 1997. Marine environmental systems, Hobart. pp. 22.Search in Google Scholar

Sanderson, J.C. and N. Barrett. 1989. A survey of the distribution of the introduced Japanese macroalga Undaria pinnatifida (Harvey) Suringer in Tasmania, December 1988. Department of Sea Fisheries, Tasmania. pp. 35.Search in Google Scholar

Scheibling, R.E. 1986. Increased macroalgal abundance following mass mortalities of sea urchins (Stronglyocentrotus droebachiensis) along the Atlantic coast of Novia Scotia. Oecologia68: 186–198.10.1007/BF00384786Search in Google Scholar PubMed

Shears, N.T. and R.C. Babcock. 2002. Marine reserves demonstrate top-down control of community structure on temperate reefs. Oecologia132: 131–142.10.1007/s00442-002-0920-xSearch in Google Scholar PubMed

Sivertsen, K. 1997. Geographic and environmental factors affecting the distribution of kelp beds and barren grounds and changes in biota associated with kelp reduction at sites along the Norwegian coast. Can. J. Fish. Aquat. Sci.54: 2872–2887.10.1139/f97-186Search in Google Scholar

Valentine, J.P. and C.R. Johnson. 2003. Establishment of the introduced kelp Undaria pinnatifida in Tasmania depends on disturbance to native algal assemblages. J. Exp. Mar. Biol. Ecol.295: 63–90.10.1016/S0022-0981(03)00272-7Search in Google Scholar

Valentine, J.P. and C.R. Johnson. 2004. Establishment of the introduced kelp Undaria pinnatifida following dieback of the native macroalga Phyllospora comosa in Tasmania, Australia. Mar. Freshwat. Res.55: 223–230.10.1071/MF03048Search in Google Scholar

Valentine, J.P. and C.R. Johnson. 2005. Persistence of the exotic kelp Undaria pinnatifida does not depend on sea urchin grazing. Mar. Ecol. Prog. Ser.285: 43–55.10.3354/meps285043Search in Google Scholar

Watanabe, J.M. and C. Harrold. 1991. Destructive grazing by sea urchins Stronglyocentrotus spp. in a central Californian kelp forest: potential roles of recruitment, depth, and predation. Mar. Ecol. Prog. Ser.71: 125–141.Search in Google Scholar

Published Online: 2005-07-05
Published in Print: 2005-04-01

© Walter de Gruyter Berlin New York

Articles in the same Issue

  1. First letters to the editor in Botanica Marina's “Forum” section
  2. Propagule release and recruitment in Porphyra perforata (Rhodophyta) from Baja California, Mexico
  3. Spatio-temporal variability of intertidal algal assemblages of the Slovenian coast (Gulf of Trieste, northern Adriatic Sea)
  4. Persistence of sea urchin (Heliocidaris erythrogramma) barrens on the east coast of Tasmania: inhibition of macroalgal recovery in the absence of high densities of sea urchins
  5. Biomass and taxonomic richness of epilithic cyanobacteria in a tropical intertidal rocky habitat
  6. Spatial variation in the structural parameters of Cymodocea nodosa seagrass meadows in the Canary Islands: a multiscaled approach
  7. The structure of sulfated galactans from selected species of New Zealand Champia
  8. The structure of the galactan from Aeodes nitidissima (Halymeniales, Rhodophyta)
  9. The structure of the polysaccharide from Grateloupia intestinalis in New Zealand
  10. Evaluation of the structures of polysaccharides from three taxa in the genus Hymenena and from Acrosorium decumbens (Rhodophyta, Delesseriaceae)
  11. The structure of polysaccharides from selected New Zealand species of Grateloupia
  12. The application of 13C NMR spectroscopy to the red algal polysaccharides of selected New Zealand species of Lomentaria
  13. Pseudovivipary, a new form of asexual reproduction in the seagrass Posidonia oceanica
  14. Comments on the papers by Ian J. Miller devoted to carbon-13 NMR spectroscopy of red algal galactans
  15. Response to “Comments on the papers by Ian J. Miller devoted to carbon-13 NMR spectroscopy of red algal galactans” by Anatolii I. Usov; Bot. Mar. 48 (2005): 178–180
  16. 8th International Phycological Congress 13–19 August 2005, Durban, South Africa
Downloaded on 16.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/BOT.2005.025/html
Scroll to top button