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Calcareous meiofauna associated with the calcareous alga Corallina officinalis on bedrock and boulder-field shores of Ceredigion, Wales, UK

Published online by Cambridge University Press:  23 December 2020

Brent Wilson Open the ORCID record for Brent Wilson [Opens in a new window]  and
Lee-Ann C. Hayek
Brent Wilson*
Affiliation:
Petroleum Geoscience Program, Department of Chemical and Process Engineering, The University of the West Indies, St. Augustine, Trinidad and Tobago Cedar Lodge, Maenygroes, Ceinewydd, Ceredigion, UK
Lee-Ann C. Hayek
Affiliation:
Smithsonian Institution, MRC-121, Washington, DC, USA
*
Author for correspondence: Brent Wilson, E-mail: brentforam@gmail.com
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Abstract

The intertidal coastline of Ceredigion, Wales, comprises a patchwork of unstable sand and cobble beaches, and stable bedrock areas and boulder-fields. The last two shoreline types support rock-pools with growths of the red alga Corallina officinalis, the thalli of which are a popular substrate for calcareous epiphytes. Replicate samples of C. officinalis (four per site) were taken from (a) three bedrock sites (Ceinewydd, Aberystwyth Victoria Rocks and Castle Rocks) and (b) three boulder-fields (Llanon, Aberaeron lower shore (Aberaeron LS), Llanina) on the lower shore. The middle shore boulder field at Aberaeron (Aberaeron MS) was also sampled. These replicates were examined for calcareous meiofauna (63–2000 μm) not previously examined as a community: spirorbids, foraminifera, gastropods, bryozoans, ostracods and ophiuroids. These were assigned to sessile and vagile modes of life. The sessile association overwhelmingly dominated bedrock coastlines and the Aberaeron MS, while the vagile association was at its most abundant on the Corallina from lower shore, stable boulder-fields. Gastropods were almost entirely limited to Corallina on boulder-fields. We hypothesize that the boulders induce low-energy turbulence among breaking waves, allowing the less firmly attached vagile meiofauna to dominate on C. officinalis in rock-pools in lower shore boulder-fields. The small attachment area of sessile organisms allows them to settle bedrock sites in greater densities than do vagile organisms at boulder-field sites, which are presumed to require larger foraging areas.

Keywords

BivalviaBryozoaforaminiferaGastropodaOstracodaSpirorbidae
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 100 , Issue 8 , December 2020 , pp. 1205 - 1217
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press on behalf of Marine Biological Association of the United Kingdom

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References

Anonymous (2013) Storm waves swamp people in street. Retrieved from https://www.bbc.co.uk/news/av/uk-wales-24807642/storm-waves-swamp-people-in-aberystwyth-street.Google Scholar
Athersuch, J, Horne, DJ and Whittaker, JE (1989) Marine and Brackish Water Ostracods (Superfamilies Cypridacea and Cytheracea). Leiden: E. J. Brill; Linnean Society and Estuarine and Brackish-Water Sciences AssociationGoogle Scholar
Atkinson, K (1969) The association of living foraminifera with algae from the littoral zone, south Cardigan Bay, Wales. Journal of Natural History 3, 517–542.CrossRefGoogle Scholar
Barrio, IC, Hik, DS, Bueno, CG and Cahill, JF (2013) Extending the stress-gradient hypothesis – is competition among animals less common in harsh environments? Oikos 122, 516–523.CrossRefGoogle Scholar
Bat, L, Akbuliut, M, Sezgn, M and Ulha, M (2001) Effects of sewage pollution the structure of the community of Ulva lactuca, Enteremorpha linza and rocky macrofauna in Disliman of Sinop. Turkish Journal of Biology 25, 93–102.Google Scholar
Bergamin, I, Romano, E, Gabellini, M, Ausili, A and Carboni, M (2003) Chemical-physical and ecological characterisation in the environmental project of a polluted coastal area: the Bagnoli case study. Mediterranean Marine Science 4, 5–20.CrossRefGoogle Scholar
Berger, WH and Parker, FL (1970) Diversity of planktonic foraminifera in deep-sea sediments. Science (New York, N.Y.) 168, 1345–1347.CrossRefGoogle ScholarPubMed
Bertness, MD and Callaway, R (1994) Positive interactions in communities. Trends in Ecology & Evolution 9, 191–193.CrossRefGoogle ScholarPubMed
Bertness, MD and Leonard, GH (1997) The role of positive interactions in communities: lessons from intertidal habitats. Ecology 78, 1976–1989.CrossRefGoogle Scholar
Best, MA and Thorpe, JP (1986) Feeding-current interactions and competition for food among the bryozoan epiphytes of Fucus serratus. Marine Biology 93, 371–375.CrossRefGoogle Scholar
Brodie, J, Walker, RH, Williamson, C and Irvine, LM (2013) Epitypification and redescription of Corallina officinalis L., the type of the genus, and C. elongata Ellis et Solander (Corallinales, Rhodophyta). Cryptogamie, Algologie 34, 49–56.CrossRefGoogle Scholar
Burrows, MT, Harvey, R and Robb, L (2008) Wave exposure indices from digital coastlines and the prediction of rocky shore community structure. Marine Ecology Progress Series 353, 1–12.CrossRefGoogle Scholar
Burrows, M, Moore, P and Hawkins, S (2009) Recommendations for intertidal biodiversity surveillance. Joint Nature Conservation Committee Report 396, 1–79.Google Scholar
Bussell, J, Lucas, I and Seed, R (2007) Patterns in the invertebrate assemblage associated with Corallina officinalis in tide pools. Journal of the Marine Biological Association of the United Kingdom 87, 383–388.CrossRefGoogle Scholar
Cabral, MC and Loureiro, IM (2013) Overview of Recent and Holocene ostracods (Crustacea) from brackish and marine environments of Portugal. Journal of Micropalaeontology 32, 135–159.CrossRefGoogle Scholar
Crisp, DJ and Mwaiseje, B (1989) Diversity in intertidal communities with special reference to the Corallina officinalis community. Scientia Marina 53, 365–372.Google Scholar
Cushman, JA (1908) Foraminifera of the Woods Hole region. Proceedings of the Boston Society of Natural History 34, 23–34.Google Scholar
Darling, KF, Schweizer, M, Knudsen, KL, Evans, KM, Bird, C, Roberts, A and Austin, WEN (2016) The genetic diversity, phylogeography and morphology of Elphidiidae (Foraminifera) in the Northeast Atlantic. Marine Micropaleontology 129, 1–23.CrossRefGoogle Scholar
Debenay, J-P, Bénéteau, E, Zhang, J, Stouff, V, Geslin, E, Redois, F and Fernandez-Gonzalez, M (1998) Ammonia beccarii and Ammonia tepida (Foraminifera): morphofunctional arguments for their distinction. Marine Micropaleontology 34, 235–244.CrossRefGoogle Scholar
de Kluijver, MJ, Ingalsuo, SS and de Bruyne, RH (n.d.) Mollusca of the North Sea. Marine Species Idenfication Portal, species-identification.org.Google Scholar
Dommasnes, A (1968) Variations in the meiofauna of Corallina officinalis L. with wave exposure. Sarsia 34, 117–124.CrossRefGoogle Scholar
Dommasnes, A (1969) On the fauna of Corallina officinalis L. in western Norway. Sarsia 38, 71–86.CrossRefGoogle Scholar
Enright, CT, Newkirk, GF, Craigie, JS and Castell, JD (1986) Evaluation of phytoplankton as diets for juvenile Ostrea edulis L. Journal of Experimental Marine Biology and Ecology 96, 1–13.CrossRefGoogle Scholar
Gabel, B (1971) Die Foraminiferen der Nordsee. Heligoland Marine Research 1971, 1–65.Google Scholar
Gee, JM (1967) Growth and breeding of Spirorbis rupestris (Polychaeta: Serpulidae). Journal of Zoology 152, 235–244.CrossRefGoogle Scholar
Goldstein, ST (2003) Foraminifera: a biological overview. In Sen Gupta, BK (ed.), Modern Foraminifera. Dordrecht: Springer, pp. 37–55.Google Scholar
Graham, A (1971) British Prosobranchs. Synopses of the British Fauna 2, 1–112.Google Scholar
Grahame, J and Hanna, FS (1989) Factors affecting the distribution of the epiphytic fauna of Corallina officinalis (L.) on an exposed rocky shore. Ophelia 30, 113–129.CrossRefGoogle Scholar
Grainger, J (2013) The community structure, and ecology, in and Around a Sabellaria alveolata biogenic reef BSc (Hons), Angela Ruskin University, UK. Retrieved from https://welshwildlife-6aa7.kxcdn.com/wp-content/uploads/cbmwc/2013/05/Justin-Grainger-honeycomb-worm-dissertation.pdf.Google Scholar
Grass, AJ (2006) Structural features of turbulent flow over smooth and rough boundaries. Journal of Fluid Mechanics 50, 233–255.CrossRefGoogle Scholar
Gruet, Y (1984) Granulometric evolution of the sand tube in relation to growth of the polychaete annelid Sabellaria alveolata (Linné) (Sabellariidae). Ophelia 23, 181–193.CrossRefGoogle Scholar
Gruet, Y (1986) Spatio-temporal changes of sabellarian reefs built by the sedentary polychaete Sabellaria alveolata (Linné). Marine Ecology 7, 303–319.CrossRefGoogle Scholar
Hardy, G and Guiry, M (2003) A Check-list and Atlas of the Seaweeds of Britain and Ireland. http://www.seaweed.ie/check-list/check-list.pdf.Google Scholar
Hart, SP and Marshall, DJ (2013) Environmental stress, facilitation, competition, and coexistence. Ecology 94, 2719–2731.CrossRefGoogle ScholarPubMed
Haynes, JR (1973) Cardigan Bay Recent foraminifera (Cruises of the R. V. Antur, 1962–1964). Bulletin of the British Museum (Natural History) Suppl. 4, 1–245.Google Scholar
Hayward, BW (1979) An intertidal Zostera pool community at Kawerua, Northland and its foraminiferal microfauna. Tane 25, 173–186.Google Scholar
Hayward, PJ and Ryland, JS (1990) Handbook of the Marine Fauna of North-West Europe. Oxford: Oxford University Press.Google Scholar
Hayward, PJ and Ryland, JS (2017) Handbook of the Marine Fauna of North-West Europe, 2nd edn. Oxford: Oxford University Press.CrossRefGoogle Scholar
He, Q, Bertness, MD and Altieri, AH (2013) Global shifts towards positive species interactions with increasing environmental stress. Ecology Letters 16, 695–706.CrossRefGoogle ScholarPubMed
Hedley, RH, Hurdle, CM and Burdett, IDJ (1967) The Marine Fauna of New Zealand: Intertidal Foraminifera of the Corallina officinalis Zone. New Zealand Department of Scientific and Industrial Research.Google Scholar
Heinz, P, Geslin, E and Hemleben, C (2005) Laboratory observations of benthic foraminiferal cysts. Marine Biology Research 1, 149–159.CrossRefGoogle Scholar
Hofker, J (1930) The Foraminifera of the Siboga Expedition, Part II: Families Astrorhizidae, Rhizamminidae, Reophacidae, Anomalinidae, Peneroplidae, with an Introduction on the Life-Cycle of the Foraminifera. Leiden: E. J. Brill.Google Scholar
Horne, DJ (1982 a) The ostracod fauna of an intertidal Sabellaria reef at Blue Anchor, Somerset, England. Estuarine, Coastal and Shelf Science 15, 671–678.CrossRefGoogle Scholar
Horne, DJ (1982 b) The vertical distribution of phytal ostracods in the intertidal zone at Gore Point, Bristol Channel. U.K. Journal of Micropalaeontology 1, 71–84.CrossRefGoogle Scholar
Hull, SL (1997) Seasonal changes in diversity and abundance of ostracods on four species of intertidal algae with differing structural complexity. Marine Ecology Progress Series 161, 71–82.CrossRefGoogle Scholar
Hull, SL (1999) Comparison of tidepool phytal ostracod abundance and assemblage structure on three spatial scales. Marine Ecology Progress Series 182, 201–208.CrossRefGoogle Scholar
Jauffrais, T, LeKieffre, C, Koho, KA, Tsuchiya, M, Schweizer, M, Bernhard, JM and Geslin, E (2018) Ultrastructure and distribution of kleptoplasts in benthic foraminifera from shallow-water (photic) habitats. Marine Micropaleontology 138, 46–62.CrossRefGoogle Scholar
Jepps, MW (2009) Studies on Polystomella Lamarck (Foraminifera). Journal of the Marine Biological Association of the United Kingdom 25, 607–666.CrossRefGoogle Scholar
Kawai, T and Tokeshi, M (2007) Testing the facilitation-competition paradigm under the stress-gradient hypothesis: decoupling multiple stress factors. Proceedings, Biological Sciences 274, 2503–2508.Google ScholarPubMed
Kelaher, BP, Chapman, MG and Underwood, AJ (2001) Spatial patterns of diverse macrofaunal assemblages in coralline turf and their associations with environmental variables. Journal of the Marine Biological Association of the United Kingdom 81, 917–930.CrossRefGoogle Scholar
Kitazato, H (1988) Ecology of benthic foraminifera in the tidal zone of a rocky shore. Revue de Paleobiologie 2, 815–825.Google Scholar
Kitazato, H (1992) Pseudopodia of benthic foraminifera and their relationships to the test morphology. In Takayanagi, V and Saito, T (eds), Studies in Benthic Foraminifera. Tokyo: Tokai University Press, pp. 103–108.Google Scholar
Knight-Jones, EW, Knight-Jones, P and Al-Ogily, SM (1975) Ecological isolation in the Spirorbidae. Paper presented at the Proceedings of the 9th European Marine Biology Symposium.Google Scholar
Langer, MR (1993) Epiphytic Foraminifera. Marine Micropaleontology 20, 235–265.CrossRefGoogle Scholar
Langer, MR and Gehring, C (1993) Bacteria farming: a possible feeding strategy of some smaller motile foraminifera. Journal of Foraminiferal Research 23, 40–46.CrossRefGoogle Scholar
Larsen, PS and Riisgård, HU (2002) On ciliary sieving and pumping in bryozoans. Journal of Sea Research 48, 181–195.CrossRefGoogle Scholar
Linke, P and Lutze, GF (1993) Microhabitat preferences of benthic foraminifera – a static concept or a dynamic adaptation to optimize food acquisition. Marine Micropaleontology 20, 215–234.CrossRefGoogle Scholar
Lipps, JH (1983) Biotic interactions in benthic foraminifera. In Tevesz, MJS and McCall, PC (eds), Biotic Interactions in Recent and Fossil Benthic Communities. New York, NY: Plenum, pp. 331–376.Google Scholar
Lister, JJ (1895) Contributions to the life history of foraminifera. Philosophical Transactions of the Royal Society of London (B) 186, 401–453.Google Scholar
Maestre, FT, Callaway, RM, Valladares, F and Lortie, CJ (2009) Refining the stress-gradient hypothesis for competition and facilitation in plant communities. Journal of Ecology 97, 199–205.CrossRefGoogle Scholar
Metaxas, A, Hunt, HL and Scheibling, RE (1994) Spatial and temporal variability of macrobenthic communities in tidepools on a rocky shore in Nova Scotia, Canada. Marine Ecology Progress Series 105, 85–103.CrossRefGoogle Scholar
Mettam, C (1994) Intertidal zonation of animals and plants on rocky shores in the Bristol Channel and Severn Estuary – the northern shores. Biological Journal of the Linnean Society 51, 123–147.Google Scholar
Morin, PJ (1999) Community Ecology. Malden, MA: Blackwell Science.Google Scholar
Muller, WA and Lee, JJ (1969) Apparent indispensability of bacteria in foraminiferan nutrition. Journal of Protozoology 16, 471–478.CrossRefGoogle Scholar
Murray, JW (1971) Atlas of British Recent Foraminiferids. New York, NY: Elsevier.Google Scholar
Murray, JW (1979) British nearshore foraminiferids: key and notes to the idenfication of the species. Synopses of the British Fauna 16, 1–68.Google Scholar
Murray, JW (2006) Ecology and Applications of Benthic Foraminifera. Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Nott, J (2003) Waves, coastal boulder deposits and the importance of the pre-transport setting. Earth and Planetary Science Letters 210, 269–276.CrossRefGoogle Scholar
Paine, RT (1969) The Pisaster–Tegula interaction: prey patches, predator food preference, and intertidal community structure. Ecology 50, 950–961.CrossRefGoogle Scholar
Paine, RT (1974) Intertidal community structure: experimental studies on the relationship between a dominant competitor and its principal predator. Oecologia 15, 93–120.CrossRefGoogle ScholarPubMed
Porter, J (2012) Seasearch Guide to Bryozoans and Hydroids of Britain and Ireland. Ross-on-Wye: Marine Conservation Society.Google Scholar
Pritchard, H (2016) Storm Imogen sends HUGE waves crashing into Aberystwyth's seafront. Retrieved from https://www.walesonline.co.uk/news/wales-news/storm-imogen-sends-huge-waves-10855507.Google Scholar
Ríos, C and Mutschke, E (1999) Community structure of intertidal boulder-cobble fields in the Straits of Magellan, Chile. Scientia Marina 63(Suppl. 1), 193–201.CrossRefGoogle Scholar
Rzhavsky, AV (1994) On the morphoecology of spirorbid tubes (Polychaeta, Spirorbidae). Ophelia 39, 177–182.CrossRefGoogle Scholar
Rzhavsky, AV, Kupriyanova, EK, Sikorski, AV and Dahle, S (2014) Calcareous Tubeworms (Polychaeta, Serpulidae) of the Arctic Ocean. Moscow: KMK Scientific Press.Google Scholar
Schönfeld, J, Alve, E, Geslin, E, Jorissen, F, Korsun, S, Spezzaferri, S and Members of the Fobimo Group (2012) The FOBIMO (FOraminiferal BIo-MOnitoring) initiative – towards a standardised protocol for soft-bottom benthic foraminiferal monitoring studies. Marine Micropaleontology 94–95, 1–13.CrossRefGoogle Scholar
Stebbing, ARD (1973) Competition for space between the epiphytes of Fucus Serratus L. Journal of the Marine Biological Association of the United Kingdom 53, 247–261.CrossRefGoogle Scholar
Stefanoudis, PV and Gooday, AJ (2016) Formation of agglutinated cysts by the foraminiferan Sphaeroidina bulloides on the Porcupine Abyssal Plain (NE Atlantic). Marine Biodiversity 46, 747–749.CrossRefGoogle Scholar
Sumi, CBT and Scheibling, RE (2005) Role of grazing by sea urchins Strongylocentrotus droebachiensis in regulating the invasive alga Codium fragile ssp. tomentosoides in Nova Scotia. Marine Ecology Progress Series 292, 203–212.CrossRefGoogle Scholar
Trier, K (1990) A preliminary study of the brackish and marine Ostracoda of the Pembrokeshire coast, S. W. Wales. In Whatley, R and Maybury, C (eds), Ostracoda and Global Events. Amsterdam: Springer, pp. 571–581.Google Scholar
Tsuchiya, M, Chikaraishi, Y, Nomaki, H, Sasaki, Y, Tame, A, Uematsu, K and Ohkouchi, N (2018) Compound-specific isotope analysis of benthic foraminifer amino acids suggests microhabitat variability in rocky-shore environments. Ecology and Evolution 8, 8380–8395.CrossRefGoogle ScholarPubMed
Vine, PJ and Bailey-Brock, JH (1984) Taxonomy and ecology of coral reef tube worms (Serpulidae, Spirorbidae) in the Sudanese Red Sea. Zoological Journal of the Linnean Society 80, 135–156.CrossRefGoogle Scholar
Wallenstein, FFMM and Neto, AI (2006) Intertidal rocky shore biotopes of the Azores: a quantitative approach. Helgoland Marine Research 60, 196–206.CrossRefGoogle Scholar
Walton, CL (1913) The shore fauna of Cardigan Bay. Journal of the Marine Biological Association of the United Kingdom 10, 102–113.CrossRefGoogle Scholar
Wells, E (n.d.) A field guide to the British seaweeds: As required for assistance in the classification of water bodies under the Water Framework Directive. Wells Marine Surveys, UK.Google Scholar
Whittaker, JE (1988) Recent & Quaternary Ostracoda of the Firth of Clyde, Southwest Scotland. British Micropalaeontological Field Guide 8, 1–50.Google Scholar
Williams, EE (1964) The growth and distribution of Gibbula umbilicalis (Da Costa) on a rocky shore in Wales. Journal of Animal Ecology 33, 433–442.CrossRefGoogle Scholar
Williams, GA (1996) Seasonal variation in a low shore Fucus serratus (Fucales, Phaeophyta) population and its epiphytic fauna. Paper presented at the Fifteenth International Seaweed Symposium, Dordrecht.CrossRefGoogle Scholar
Wilson, B (2010) Effect of hurricanes on guilds of nearshore epiphytal foraminifera, Nevis, West Indies. Journal of Foraminiferal Research 40, 327–343.CrossRefGoogle Scholar
Wilson, B and Hayek, LC (2019) Benthic foraminifera and the polychaete Sabellaria alveolata (Linnaeus, 1767) on the intertidal rocky shore at Ceinewydd, Ceredigion, Wales, UK. Marine Micropaleontology 146, 51–58.CrossRefGoogle Scholar
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