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information on the biology of species and the ecology of habitats found around the coasts and seas of the British Isles

Filamentous red seaweeds, sponges and Balanus crenatus on tide-swept variable-salinity infralittoral rock

03-04-2018

Summary

UK and Ireland classification

UK and Ireland classification

Description

Tide-swept infralittoral rock subject to variable salinity and turbid waters occurs in the mid to upper reaches of the rias of south-west Britain, where riverine freshwater input reduces the salinity. Very shallow rock under these conditions is characterized by a covering of filamentous red seaweed such as Callithamnion spp., Antithamnion spp., Ceramium spp., Griffithsia devoniensis, Pterothamnion plumula and Polysiphonia fucoides, as well as the filamentous green seaweed Cladophora spp. Foliose red seaweeds such as Hypoglossum hypoglossoides, Cryptopleura ramosa and Erythroglossum laciniatum commonly occur, as does the foliose green seaweed Ulva lactuca. Although Saccharina latissima is often present it is usually in very low abundance (Occasional). The fluctuating salinity limits the number of species able to exist in this habitat. The animal community is dominated by the sponges Halichondria panicea and Hymeniacidon perleve and the barnacle Balanus crenatus. The ascidians Clavelina lepadiformis and Dendrodoa grossularia can be locally abundant at some sites. The crab Carcinus maenas is usually present, as is the mussel Mytilus edulis. The bryozoan Crisularia plumosa is sometimes present. Where vertical rock is present, the seaweeds Ceramium nodulosum, Pterothamnion plumula, Cryptopleura ramosa, Hypoglossum hypoglossoides and Erythroglossum laciniatum are typically found (JNCC, 2015).

Depth range

0-5 m

Additional information

None

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Sensitivity reviewHow is sensitivity assessed?

Explanation

None

Species indicative of sensitivity

-

Physical Pressures

No sensitivity data available

Chemical Pressures

No sensitivity data available

Biological Pressures

No sensitivity data available

Additional information

No text entered.

Bibliography

  1. Ackers, R.G.A., Moss, D. & Picton, B.E. 1992. Sponges of the British Isles (Sponges: V): a colour guide and working document. Ross-on-Wye: Marine Conservation Society.

  2. Airoldi, L., 2003. The effects of sedimentation on rocky coast assemblages. Oceanography and Marine Biology: An Annual Review, 41,161-236

  3. Aneiros, F., Rubal, M., Troncoso, J.S. & Bañón, R., 2015. Subtidal benthic megafauna in a productive and highly urbanised semi-enclosed bay (Ría de Vigo, NW Iberian Peninsula). Continental Shelf Research, 110, 16-24.

  4. Balata, D., Piazzi, L., & Cinelli, F., 2007. Increase of sedimentation in a subtidal system: effects on the structure and diversity of macroalgal assemblages. Journal of Experimental Marine Biology and Ecology351(1), 73-82.

  5. Barnes, H. & Barnes, M., 1968. Egg numbers, metabolic efficiency and egg production and fecundity; local and regional variations in a number of common cirripedes. Journal of Experimental Marine Biology and Ecology, 2, 135-153.

  6. Barnes, H. & Powell, H.T., 1953. The growth of Balanus balanoides and B. crenatus under varying conditions of submersion. Journal of the Marine Biological Association of the United Kingdom, 32, 107-127.

  7. Barthel, D., 1986. On the ecophysiology of the sponge Halichondria panicea in Kiel Bight. I. Substrate specificity, growth and reproduction. Marine Ecology Progress Series, 32, 291-298.

  8. Bauvais, C., Zirah, S., Piette, L., Chaspoul, F., Domart-Coulon, I., Chapon, V., Gallice, P., Rebuffat, S., Pérez, T. & Bourguet-Kondracki, M.-L., 2015. Sponging up metals: bacteria associated with the marine sponge Spongia officinalis. Marine Environmental Research, 104, 20-30.

  9. Bell, J.J. & Barnes, D.K., 2000. The distribution and prevalence of sponges in relation to environmental gradients within a temperate sea lough: inclined cliff surfaces. Diversity and Distributions, 6 (6), 305-323.

  10. Bell, J.J. & Smith, D., 2004. Ecology of sponge assemblages (Porifera) in the Wakatobi region, south-east Sulawesi, Indonesia: richness and abundance. Journal of the Marine Biological Association of the UK, 84 (3), 581-591.

  11. Boller, M.L. & Carrington, E., 2006. In situ measurements of hydrodynamic forces imposed on Chondrus crispus Stackhouse. Journal of Experimental Marine Biology and Ecology, 337 (2), 159-170.

  12. Boller, M.L. & Carrington, E., 2007. Interspecific comparison of hydrodynamic performance and structural properties among intertidal macroalgae. Journal of Experimental Biology, 210 (11), 1874-1884.

  13. Boney, A.D., 1971. Sub-lethal effects of mercury on marine algae. Marine Pollution Bulletin, 2, 69-71.

  14. Brault, S. & Bourget, E., 1985. Structural changes in an estuarine subtidal epibenthic community: biotic and physical causes. Marine Ecology Progress Series, 21, 63-73.

  15. Bryan, G.W., 1984. Pollution due to heavy metals and their compounds. In Marine Ecology: A Comprehensive, Integrated Treatise on Life in the Oceans and Coastal Waters, vol. 5. Ocean Management, part 3, (ed. O. Kinne), pp.1289-1431. New York: John Wiley & Sons.

  16. Bulleri, F. & Airoldi, L., 2005. Artificial marine structures facilitate the spread of a non‐indigenous green alga, Codium fragile ssp. tomentosoides, in the north Adriatic Sea. Journal of Applied Ecology, 42 (6), 1063-1072.

  17. Castric-Fey, A. & Chassé, C., 1991. Factorial analysis in the ecology of rocky subtidal areas near Brest (west Brittany, France). Journal of the Marine Biological Association of the United Kingdom, 71, 515-536.

  18. Chamberlain, Y.M., 1996. Lithophylloid Corallinaceae (Rhodophycota) of the genera Lithophyllum and Titausderma from southern Africa. Phycologia, 35, 204-221.

  19. Clark, R.B., 1997. Marine Pollution, 4th ed. Oxford: Carendon Press.

  20. Cole, S., Codling, I.D., Parr, W., Zabel, T., 1999. Guidelines for managing water quality impacts within UK European marine sites [On-line]. UK Marine SACs Project. [Cited 26/01/16]. Available from: http://www.ukmarinesac.org.uk/pdfs/water_quality.pdf

  21. Coleman, R.A., Hoskin, M.G., von Carlshausen, E. & Davis, C.M., 2013. Using a no-take zone to assess the impacts of fishing: Sessile epifauna appear insensitive to environmental disturbances from commercial potting. Journal of Experimental Marine Biology and Ecology, 440, 100-107.

  22. Colhart, B.J., & Johanssen, H.W., 1973. Growth rates of Corallina officinalis (Rhodophyta) at different temperatures. Marine Biology, 18, 46-49.

  23. Connor, D.W., Allen, J.H., Golding, N., Howell, K.L., Lieberknecht, L.M., Northen, K.O. & Reker, J.B., 2004. The Marine Habitat Classification for Britain and Ireland. Version 04.05. Joint Nature Conservation Committee, Peterborough. www.jncc.gov.uk/MarineHabitatClassification.

  24. Davenport, J. & Davenport, J.L., 2005. Effects of shore height, wave exposure and geographical distance on thermal niche width of intertidal fauna. Marine Ecology Progress Series, 292, 41-50.

  25. Davison, I.R., 1991. Environmental effects on algal photosynthesis: temperature. Journal of Phycology, 27 (1), 2-8.

  26. Drew, E.A., Forster, G.R., Gage, J., Harwood, G., Larkum, A.W.D., Lythgoe, J.M & Potts, G.W. 1967. "Torrey Canyon" report. Underwater Association Report for 1966-67, pp. 53-60.

  27. Eckman, J.E. & Duggins, D.O., 1993. Effects of flow speed on growth of benthic suspension feeders. Biological Bulletin, 185, 28-41.

  28. Firth, L.B., Thompson, R.C., White, F.J., Schofield, M., Skov, M.W., Hoggart, S.P.G., Jackson, J., Knights, A.M. & Hawkins, S.J., 2013. The importance of water-retaining features for biodiversity on artificial intertidal coastal defence structures. Diversity and Distributions, 19 (10), 1275-1283.

  29. Fish, J.D. & Fish, S., 1996. A student's guide to the seashore. Cambridge: Cambridge University Press.

  30. Freese, L., Auster, P.J., Heifetz, J. & Wing, B.L., 1999. Effects of trawling on seafloor habitat and associated invertebrate taxa in the Gulf of Alaska. Marine Ecology Progress Series, 182, 119-126.

  31. Gerrodette, T. & Flechsig, A., 1979. Sediment-induced reduction in the pumping rate of the tropical sponge Verongia lacunosa. Marine Biology, 55 (2), 103-110.

  32. Gessner, F., 1970. Temperature - Plants. In Marine Ecology: A Comprehensive Treatise on Life in Oceans and Coastal Waters. Vol. 1 Environmental Factors Part 1. (ed. O. Kinne), pp. 363-406. Chichester: John Wiley & Sons

  33. Gittenberger, A. & Van Loon, W.M.G.M., 2011. Common Marine Macrozoobenthos Species in the Netherlands, their Characterisitics and Sensitivities to Environmental Pressures. GiMaRIS report no 2011.08.

  34. Gorostiaga, J. & Diez, I., 1996. Changes in the sublittoral benthic marine macroalgae in the polluted area of Abra de Bilbao and proximal coast (Northern Spain). Marine Ecology Progress Series130 (1), 157-167.

  35. Grandy, N., 1984. The effects of oil and dispersants on subtidal red algae. Ph.D. Thesis. University of Liverpool.

  36. Green, D., Chapman, M. & Blockley, D., 2012. Ecological consequences of the type of rock used in the construction of artificial boulder-fields. Ecological Engineering, 46, 1-10.

  37. Guiry, M.D. & Guiry, G.M. 2015. AlgaeBase [Online], National University of Ireland, Galway [cited 30/6/2015]. Available from: http://www.algaebase.org/

  38. Hatcher, A.M., 1998. Epibenthic colonization patterns on slabs of stabilised coal-waste in Poole Bay, UK. Hydrobiologia, 367, 153-162.

  39. Hiscock, S. & Maggs, C.A., 1984. Notes on the distribution and ecology of some new and interesting seaweeds from south-west Britain. British Phycological Journal, 19 (1), 73-87.

  40. Hoare, R. & Hiscock, K., 1974. An ecological survey of the rocky coast adjacent to the effluent of a bromine extraction plant. Estuarine and Coastal Marine Science, 2 (4), 329-348.

  41. Holme, N.A. & Wilson, J.B., 1985. Faunas associated with longitudinal furrows and sand ribbons in a tide-swept area in the English Channel. Journal of the Marine Biological Association of the United Kingdom, 65, 1051-1072.

  42. Husa, V., 2007. Effects of increased sea temperatures on macro algae. Marine Research News14, 1-2.

  43. Huthnance, J., 2010. Ocean Processes Feeder Report. London, DEFRA on behalf of the United Kingdom Marine Monitoring and Assessment Strategy (UKMMAS) Community.

  44. Hyslop, B.T. & Davies, M.S., 1998. Evidence for abrasion and enhanced growth of Ulva lactuca L. in the presence of colliery waste particles. Environmental Pollution, 101 (1), 117-121.

  45. JNCC, 2015. The Marine Habitat Classification for Britain and Ireland Version 15.03. JNCC: JNCC. 2015(20/05/2015). jncc.defra.gov.uk/MarineHabitatClassification

  46. Kain, J.M., 1982. The reproductive phenology of nine species of the Rhodophycota in the subtidal region of the Isle of Man. British Phycological Journal, 17, 321-331.

  47. Kenny, A.J. & Rees, H.L., 1994. The effects of marine gravel extraction on the macrobenthos: early post dredging recolonisation. Marine Pollution Bulletin, 28, 442-447.

  48. Kitching, J.A., 1937. Studies in sublittoral ecology. II Recolonization at the upper margin of the sublittoral region; with a note on the denudation of Laminaria forest by storms. Journal of Ecology, 25, 482-495.

  49. Krause-Jensen, D., Carstensen, J. & Dahl, K., 2007. Total and opportunistic algal cover in relation to environmental variables. Marine Pollution Bulletin, 55 (1–6), 114-125.

  50. Lohrmann, N.L., Logan, B.A. & Johnson, A.S., 2004. Seasonal acclimatization of antioxidants and photosynthesis in Chondrus crispus and Mastocarpus stellatus, two co-occurring red algae with differing stress tolerances. The Biological Bulletin, 207 (3), 225-232.

  51. Lüning, K. & Dring, M.J., 1975. Reproduction, growth and photosynthesis of gametophytes of Laminaria saccharina grown in blue and red light. Marine Biology, 29, 195-200.

  52. Marques, D., Almeida, M., Xavier, J. & Humanes, M., 2007. Biomarkers in marine sponges: acetylcholinesterase in the sponge Cliona celata. Porifera Research: Biodiversity, Innovation and Sustainability. Série Livros, 28, 427-432.

  53. Miron, G., Bourget, E. & Archambault, P., 1996. Scale of observation and distribution of adult conspecifics: their influence in assessing passive and active settlement mechanisms in the barnacle Balanus crenatus (Brugière). Journal of Experimental Marine Biology and Ecology, 201 (1), 137-158.

  54. Naranjo, S.A., Carballo, J.L., & Garcia-Gomez, J.C., 1996. Effects of environmental stress on ascidian populations in Algeciras Bay (southern Spain). Possible marine bioindicators? Marine Ecology Progress Series, 144 (1), 119-131.

  55. Naylor, E., 1965. Effects of heated effluents upon marine and estuarine organisms. Advances in Marine Biology, 3, 63-103.

  56. Newman, W. A. & Ross, A., 1976. Revision of the Balanomorph barnacles including a catalogue of the species. San Diego Society of Natural History Memoirs, 9, 1–108.

  57. Norton, T.A., 1992. Dispersal by macroalgae. British Phycological Journal, 27, 293-301.

  58. O'Brien, P.J. & Dixon, P.S., 1976. Effects of oils and oil components on algae: a review. British Phycological Journal, 11, 115-142.

  59. Rai, L., Gaur, J.P. & Kumar, H.D., 1981. Phycology and heavy-metal pollution. Biological Reviews, 56, 99-151.

  60. Rice, H., Leighty, D.A. & McLeod, G.C., 1973. The effects of some trace metals on marine phytoplankton. CRC Critical Review in Microbiology, 3, 27-49.

  61. Salman, S., 1982. Seasonal and short-term variations in abundance of barnacle larvae near the south-west of the Isle of Man. Estuarine, Coastal and Shelf Science, 15 (3), 241-253.

  62. Schönberg, C.H.L., 2015. Happy relationships between marine sponges and sediments–a review and some observations from Australia. Journal of the Marine Biological Association of the United Kingdom, 1-22.

  63. Smith, J.E. (ed.), 1968. 'Torrey Canyon'. Pollution and marine life. Cambridge: Cambridge University Press.

  64. Sousa-Dias, A. & Melo, R.A., 2008. Long-term abundance patterns of macroalgae in relation to environmental variables in the Tagus Estuary (Portugal). Estuarine, Coastal and Shelf Science, 76 (1), 21-28.

  65. Storr, J.F. 1976. Ecological factors controlling sponge distribution in the Gulf of Mexico and the resulting zonation. In Aspects of Sponge Biology (ed. F.W. Harrison & R.R. Cowden), pp. 261-276. New York: Academic Press.

  66. Sweet, N.S. 2011j. Green sea-fingers (tomentosoides), Codium fragile subsp. tomentosoides. Great Britain Non-native Species Secretariat. [cited 16/06/2015]. Available from: <http://www.nonnativespecies.org

  67. Sweet N.S., 2011i. Freshwater hydroid, Cordylophora caspia. GB Non-native species secretariat, [On-line]. [cited 24/02/16]. Available from:

  68. Tillin, H. & Tyler-Walters, H., 2014. Assessing the sensitivity of subtidal sedimentary habitats to pressures associated with marine activities. Phase 2 Report – Literature review and sensitivity assessments for ecological groups for circalittoral and offshore Level 5 biotopes. JNCC Report No. 512B,  260 pp. Available from: www.marlin.ac.uk/publications

  69. Tolhurst, L.E., Barry, J., Dyer, R.A. & Thomas, K.V., 2007. The effect of resuspending sediment contaminated with antifouling paint particles containing Irgarol 1051 on the marine macrophyte Ulva intestinalis. Chemosphere, 68 (8), 1519-1524.

  70. UKTAG, 2014. UK Technical Advisory Group on the Water Framework Directive [online]. Available from: http://www.wfduk.org

  71. Vadas, R.L., Keser, M. & Rusanowski, P.C., 1976. Influence of thermal loading on the ecology of intertidal algae. In Thermal Ecology II, (eds. G.W. Esch & R.W. McFarlane), ERDA Symposium Series (Conf-750425, NTIS), Augusta, GA, pp. 202-212.

  72. Vethaak, A.D., Cronie, R.J.A. & van Soest, R.W.M., 1982. Ecology and distribution of two sympatric, closely related sponge species, Halichondria panicea (Pallas, 1766) and H. bowerbanki Burton, 1930 (Porifera, Demospongiae), with remarks on their speciation. Bijdragen tot de Dierkunde, 52, 82-102.

  73. Vidaver, W., 1972. Dissolved gases - plants. In Marine Ecology. Volume 1. Environmental factors (3), (ed. O. Kinne), 1471-1490. Wiley-Interscience, London.

  74. Witt, J., Schroeder, A., Knust, R. & Arntz, W.E., 2004. The impact of harbour sludge disposal on benthic macrofauna communities in the Weser estuary. Helgoland Marine Research, 58 (2), 117-128.

  75. Wulff, J., 2006. Resistance vs recovery: morphological strategies of coral reef sponges. Functional Ecology, 20 (4), 699-708.

Citation

This review can be cited as:

Tillin, H.M. 2016. Filamentous red seaweeds, sponges and [Balanus crenatus] on tide-swept variable-salinity infralittoral rock. In Tyler-Walters H. and Hiscock K. (eds) Marine Life Information Network: Biology and Sensitivity Key Information Reviews, [on-line]. Plymouth: Marine Biological Association of the United Kingdom. [cited 19-06-2018]. Available from: http://www.marlin.ac.uk/habitat/detail/218

Last Updated: 16/06/2016