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Marine Biology

, 165:172 | Cite as

Biological characteristics of the rafting bivalve Gaimardia trapesina in the Southern Ocean

  • Eleonora Puccinelli
  • Charles E. O. von der Meden
  • Christopher D. McQuaid
  • Isabelle J. Ansorge
Original paper

Abstract

Rafting invertebrate species represent an important link for the dispersal and colonisation of islands in the Southern Ocean. They are sensitive to changes in hydrodynamics through effects on transport and food availability, particularly in the case of filter-feeding species. This gives them the potential to act as sentinels of environmental change. The rafting kelp-associated Gaimardia trapesina is one such species, widely distributed in the Southern Ocean. In 2015 and 2016, the size structure, diet, and distribution of G. trapesina were examined around the Sub-Antarctic Prince Edward Islands (PEI) to establish benchmark data and explore their potential use for monitoring long-term change. Gaimardia trapesina and its potential food sources were collected and analysed for size structure, attachment strength, and diet, using stable isotope and fatty acid analyses. The populations examined were dominated by relatively small individuals. The strength of attachment to kelp blades was low and the byssal threads showed high elasticity. The PEI lie in the path of the west–east flowing Antarctic Circumpolar Current and the highest abundances of G. trapesina were found on the downstream sides of both islands, while the species was absent from the western, upstream coasts. Both diet analyses and SIAR mixing models indicated that G. trapesina feeds on suspended particulate matter, while kelp particles contribute minimally to the diet. Considering the wide distribution of G. trapesina, its importance as food for birds and fish, and its sensitivity to environmental conditions, there is good potential to use this species as an indicator of environmental change in the Southern Ocean.

Notes

Acknowledgements

This work was supported by funding from the South African Research Chairs Initiative of the Department of Science and Technology, the National Research Foundation, the South African Department of Environmental Affairs and Tourism, and the South African National Antarctic Program (SANAP). We acknowledge the Stable Isotope Laboratory of the Mammal Research Institute, University of Pretoria, and the InnoVenton and the Downstream Chemicals Technology Station of the Nelson Mandela Metropolitan University, where the analyses were conducted. Special thanks go to Captain Syndercombe and Captain Bengu, and the officers and crew of the SA Agulhas II for their tireless assistance at sea.

Funding

This study was funded by South African National Antarctic Program (SANAP) awarded to Prof. Isabelle J. Ansorge, and by the South African Research Chairs Initiative of the Department of Science and Technology and the National Research Foundation of South Africa, awarded to Prof. Christopher D. McQuaid.

Compliance with ethical standards

Conflict of interest

All authors have declared that no competing interests exist.

Ethical approval

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed. In addition, the permit to work on G. trapesina at the Prince Edward Islands was obtained by the Department of Environmental Affair of South Africa.

Supplementary material

227_2018_3430_MOESM1_ESM.docx (5.7 mb)
Supplementary material 1 (DOCX 5861 kb)

References

  1. Ackman RG (2002) The gas chromatograph in practical analyses of common and uncommon fatty acids for the 21st century. Anal Chim Acta 465:175–192.  https://doi.org/10.1016/s0003-2670(02)00098-3 CrossRefGoogle Scholar
  2. Adami ML, Gordillo S (1999) Structure and dynamics of the biota associated with Macrocystis pyrifera (Phaeophyta) from the Beagle Channel, Tierra del Fuego. Sci Mar 63:183–191.  https://doi.org/10.3989/scimar.1999.63s1183 CrossRefGoogle Scholar
  3. Alkanani T, Parrish CC, Thompson RJ, McKenzie CH (2007) Role of fatty acids in cultured mussels, Mytilus edulis, grown in Notre Dame Bay, Newfoundland. J Exp Mar Biol Ecol 348:33–45.  https://doi.org/10.1016/j.jembe.2007.02.017 CrossRefGoogle Scholar
  4. Allan LE, Froneman WP, Durgadoo JV, McQuaid CD, Ansorge IJ, Richoux NB (2013) Critical indirect effects of climate change on sub-Antarctic ecosystem functioning. Ecol Evol 3:2994–3004.  https://doi.org/10.1002/ece3.678 CrossRefGoogle Scholar
  5. Anderson MJ (2001) A new method for non-parametric multivariate analysis of variance. Austr Ecol 26:32–46.  https://doi.org/10.1111/j.1442-9993.2001.01070.pp.x CrossRefGoogle Scholar
  6. Anderson M, Braak CT (2003) Permutation tests for multi-factorial analysis of variance. J Stat Comput Simul 73:85–113.  https://doi.org/10.1080/00949650215733 CrossRefGoogle Scholar
  7. Ansorge IJ, Lutjeharms JRE (2002) The hydrography and dynamics of the ocean environment of the Prince Edward Islands (Southern Ocean). J Mar Syst 37:107–127.  https://doi.org/10.1016/s0924-7963(02)00198-7 CrossRefGoogle Scholar
  8. Ansorge IJ, Froneman PW, Pakhomov EA, Lutjeharms JRE, Perissinotto R, van Ballegooyen RC (1999) Physical-biological coupling in the waters surrounding the Prince Edward Islands (Southern Ocean). Polar Biol 21:135–145.  https://doi.org/10.1007/s003000050344 CrossRefGoogle Scholar
  9. Ansorge IJ, Durgadoo JV, Treasure AM (2014) Sentinels to climate change. The need for monitoring at South Africa’s Subantarctic laboratory. S Afr J Sci 110:1–4CrossRefGoogle Scholar
  10. Barnes DKA, Linse K, Waller C, Morely S, Enderlein P, Fraser KPP, Brown M (2006) Shallow benthic fauna communities of South Georgia Island. Polar Biol 29:223–228.  https://doi.org/10.1007/s00300-005-0042-0 CrossRefGoogle Scholar
  11. Bell E, Gosline J (1996) Mechanical design of mussel byssus: material yield enhances attachment strength. J Exp Biol 199:1005–1017PubMedGoogle Scholar
  12. Blankley WO (1981) Marine food of Kelp Gulls, Lesser Sheathbills and Imperial Cormorants at Marion Island (Subantarctic). Mar Ornithol 9:77–84Google Scholar
  13. Boden BP (1988) Observations of the island mass effect in the Prince Edward archipelago. Polar Biol 9:61–68.  https://doi.org/10.1007/bf00441765 CrossRefGoogle Scholar
  14. Budge SM, Iverson SJ, Koopman HN (2006) Studying trophic ecology in marine ecosystems using fatty acids: a primer on analysis and interpretation. Mar Mamm Sci 22:759–801.  https://doi.org/10.1111/j.1748-7692.2006.00079.x CrossRefGoogle Scholar
  15. Bustamante RH, Branch GM (1996) The dependence of intertidal consumers on kelp-derived organic matter on the west coast of South Africa. J Exp Mar Biol Ecol 196:1–28.  https://doi.org/10.1016/0022-0981(95)00093-3 CrossRefGoogle Scholar
  16. Castilla JC, Guiñez R (2000) Disjoint geographical distribution of intertidal and nearshore benthic invertebrates in the southern hemisphere. Rev Chil Hist Nat 73:585–603Google Scholar
  17. Christaki U, Dolan JR, Pelegri S, Rassoulzadegan F (1998) Consumption of picoplankton-size particles by marine ciliates: effects of physiological state of the ciliate and particle quality. Limnol Oceanogr 43:458–464.  https://doi.org/10.4319/lo.1998.43.3.0458 CrossRefGoogle Scholar
  18. Connell JH (1985) The consequences of variation in initial settlement vs. post-settlement mortality in rocky intertidal communities. J Exp Mar Biol Ecol 93:11–45.  https://doi.org/10.1016/0022-0981(85)90146-7 CrossRefGoogle Scholar
  19. Copeman LA, Parrish CC (2003) Marine lipids in a cold coastal ecosystem: Gilbert Bay, Labrador. Mar Biol 143:1213–1227.  https://doi.org/10.1007/s00227-003-1156-y CrossRefGoogle Scholar
  20. Cowen RK, Sponaugle S (2009) Larval dispersal and marine population connectivity. Annu Rev Mar Sci 1:443–466.  https://doi.org/10.1146/annurev.marine.010908.163757 CrossRefGoogle Scholar
  21. Cowen RK, Lwiza KMM, Sponaugle S, Paris CB, Olson DB (2000) Connectivity of marine populations: open or closed? Science 287:857–859.  https://doi.org/10.1126/science.287.5454.857 CrossRefPubMedGoogle Scholar
  22. Daly KL (1990) Overwintering development, growth, and feeding of larval Euphausia superba in the Antarctic marginal ice zone. Limnol Oceanogr 35:1564–1576.  https://doi.org/10.4319/lo.1990.35.7.1564 CrossRefGoogle Scholar
  23. Davenport J, Wilson PC (1995) Mobility, gregariousness and attachment in four small bivalve mollusc species at Husvik, South Georgia. J Molluscan Stud 61:491–498.  https://doi.org/10.1093/mollus/61.4.491 CrossRefGoogle Scholar
  24. De Villiers AF (1976) Littoral ecology of Marion and Prince Edward islands (Southern Ocean). S Afr Tydskr Antarkt Nav 4:1–40Google Scholar
  25. DeLong EF, Yayanos AA (1986) Biochemical function and ecological significance of novel bacterial lipids in deep-sea procaryotes. Appl Environ Microbiol 51:730–737PubMedPubMedCentralGoogle Scholar
  26. Denny MW (1987) Lift as a mechanism of patch initiation in mussel beds. J Exp Mar Biol Ecol 113:231–245.  https://doi.org/10.1016/0022-0981(87)90103-1 CrossRefGoogle Scholar
  27. Dunton KH, Schell DM (1987) Dependence of consumers on macroalgal (Laminaria solidungula) carbon in an arctic kelp community: δ13C evidence. Mar Biol 93:615–625.  https://doi.org/10.1007/bf00392799 CrossRefGoogle Scholar
  28. Figueiras FG, Labarta U, Reiriz MJF (2002) Coastal upwelling, primary production and mussel growth in the Rías Baixas of Galicia. In: Vadstein O, Olsen Y (eds) Sustainable increase of marine harvesting: fundamental mechanisms and new concepts. Springer, Netherlands, pp 121–131CrossRefGoogle Scholar
  29. Fraser CI, Nikula R, Waters JM (2011) Oceanic rafting by a coastal community. Proc R Soc B Biol Sci 278:649–655.  https://doi.org/10.1098/rspb.2010.1117 CrossRefGoogle Scholar
  30. Fredriksen S (2003) Food web studies in a Norwegian kelp forest based on stable isotope (δ13C and δ15N) analysis. Mar Ecol Prog Ser 260:71–81CrossRefGoogle Scholar
  31. Fyfe JC, Saenko OA (2005) Human-induced change in the Antarctic circumpolar current. J Clim 18:3068–3073.  https://doi.org/10.1175/jcli3447.1 CrossRefGoogle Scholar
  32. Glémet HC, Gerrits MF, Ballantyne JS (1997) Membrane lipids of red muscle mitochondria from land-locked and sea-run Arctic char, Salvelinus alpinus. Mar Biol 129:673–679.  https://doi.org/10.1007/s002270050210 CrossRefGoogle Scholar
  33. Gon O, Heemstra PC (1990) Fishes of the Southern Ocean. J.L.B. Smith Institute of Ichthyology, GrahamstownCrossRefGoogle Scholar
  34. Gutow L, Giménez L, Boos K, Saborowski R (2009) Rapid changes in the epifaunal community after detachment of buoyant benthic macroalgae. J Mar Biol Assoc UK 89:323–328.  https://doi.org/10.1017/s0025315408002658 CrossRefGoogle Scholar
  35. Hanson CE, Hyndes GA, Wang SF (2010) Differentiation of benthic marine primary producers using stable isotopes and fatty acids: implications to food web studies. Aquat Bot 93:114–122.  https://doi.org/10.1016/j.aquabot.2010.04.004 CrossRefGoogle Scholar
  36. Harley CDG, Randall Hughes A, Hultgren KM, Miner BG, Sorte CJB, Thornber CS, Rodriguez LF, Tomanek L, Williams SL (2006) The impacts of climate change in coastal marine systems. Ecol Lett 9:228–241.  https://doi.org/10.1111/j.1461-0248.2005.00871.x CrossRefPubMedGoogle Scholar
  37. Harmelin-Vivien M, Loizeau V, Mellon C, Beker B, Arlhac D, Bodiguel X, Ferraton F, Hermand R, Philippon X, Salen-Picard C (2008) Comparison of C and N stable isotope ratios between surface particulate organic matter and microphytoplankton in the Gulf of Lions (NW Mediterranean). Cont Shelf Res 28:1911–1919.  https://doi.org/10.1016/j.csr.2008.03.002 CrossRefGoogle Scholar
  38. Helmuth B, Veit RR, Holberton R (1994) Long-distance dispersal of a subantarctic brooding bivalve (Gaimardia trapesina) by kelp-rafting. Mar Biol 120:421–426.  https://doi.org/10.1007/bf00680216 CrossRefGoogle Scholar
  39. Helmuth B, Kingsolver JG, Carrington E (2005) Biophysics, physiological ecology, and climate change: does mechanism matter? Annu Rev Physiol 67:177–201.  https://doi.org/10.1146/annurev.physiol.67.040403.105027 CrossRefPubMedGoogle Scholar
  40. Hill JM, McQuaid CD (2009) Variability in the fractionation of stable isotopes during degradation of two intertidal red algae. Estuar Coast Shelf Sci 82:397–405.  https://doi.org/10.1016/j.ecss.2009.02.001 CrossRefGoogle Scholar
  41. Hill JM, McQuaid CD, Kaehler S (2006) Biogeographic and nearshore–offshore trends in isotope ratios of intertidal mussels and their food sources around the coast of southern Africa. Mar Ecol Prog Ser 318:63–73.  https://doi.org/10.3354/meps318063 CrossRefGoogle Scholar
  42. Hockey PAR (1988) Kelp gulls Larus dominicanus as predators in kelp Macrocystis pyrifera beds. Oecologia 76:155–157.  https://doi.org/10.1007/bf00379614 CrossRefPubMedGoogle Scholar
  43. Hoffmann LJ, Peeken I, Lochte K, Assmy P, Veldhuis M (2006) Different reactions of Southern Ocean phytoplankton size classes to iron fertilization. Limnol Oceanogr 51:1217–1229.  https://doi.org/10.4319/lo.2006.51.3.1217 CrossRefGoogle Scholar
  44. Hunt BPV, Gurney LJ, Pakhomov EA (2008) Time-series analysis of hydrological and biological variability on the Prince Edward Island (Southern Ocean) shelf. Polar Biol 31:893–904CrossRefGoogle Scholar
  45. Indarti E, Majid MIA, Hashim R, Chong A (2005) Direct FAME synthesis for rapid total lipid analysis from fish oil and cod liver oil. J Food Compos Anal 18:161–170.  https://doi.org/10.1016/j.jfca.2003.12.007 CrossRefGoogle Scholar
  46. Ituarte C (2009) Unusual modes of oogenesis and brooding in bivalves: the case of Gaimardia trapesina (Mollusca: Gaimardiidae). Invertebr Biol 128:243–251.  https://doi.org/10.1111/j.1744-7410.2009.00171.x CrossRefGoogle Scholar
  47. Ituarte CF, Cremonte F, Deferrari G (2001) Mantle-shell complex reactions elicited by digenean metacercariae in Gaimardia trapesina (Bivalvia: Gaimardiidae) from the Southwestern Atlantic Ocean and Magellan Strait. Dis Aquat Organ 48:47–56.  https://doi.org/10.3354/dao048047 CrossRefPubMedGoogle Scholar
  48. Kaehler S, Pakhomov EA, McQuaid CD (2000) Trophic structure of the marine food web at the Prince Edward Islands (Southern Ocean) determined by δ13C and δ15N analysis. Mar Ecol Prog Ser 208:13–20.  https://doi.org/10.3354/meps208013 CrossRefGoogle Scholar
  49. Kaehler S, Pakhomov E, Kalin R, Davis S (2006) Trophic importance of kelp-derived suspended particulate matter in a through-flow sub-Antarctic system. Mar Ecol Prog Ser 316:17–22.  https://doi.org/10.3354/meps316017 CrossRefGoogle Scholar
  50. Kelly MS, Hunter AJ, Scholfield CL, McKenzie JD (2000) Morphology and survivorship of larval Psammechinus miliaris (Gmelin) (Echinodermata: Echinoidea) in response to varying food quantity and quality. Aquaculture 183:223–240.  https://doi.org/10.1016/s0044-8486(99)00296-3 CrossRefGoogle Scholar
  51. Kenny R, Haysom N (1962) Ecology of rocky shore organisms at Macquarie Island. Pac Sci 16:245–263Google Scholar
  52. Kinlan BP, Gaines SD, Lester SE (2005) Propagule dispersal and the scales of marine community process. Divers Distrib 11:139–148.  https://doi.org/10.1111/j.1366-9516.2005.00158.x CrossRefGoogle Scholar
  53. Kobak J, Kakareko T (2011) The effectiveness of the induced anti-predator behaviour of zebra mussel Dreissena polymorpha in the presence of molluscivorous roach Rutilus rutilus. Aquat Ecol 45:357–366.  https://doi.org/10.1007/s10452-011-9359-7 CrossRefGoogle Scholar
  54. Konotchick T, Parnell PE, Dayton PK, Leichter JJ (2012) Vertical distribution of Macrocystis pyrifera nutrient exposure in southern California. Estuar Coast Shelf Sci 106:85–92.  https://doi.org/10.1016/j.ecss.2012.04.026 CrossRefGoogle Scholar
  55. Leese F, Agrawal S, Held C (2010) Long-distance island hopping without dispersal stages: transportation across major zoogeographic barriers in a Southern Ocean isopod. Naturwissenschaften 97:583–594.  https://doi.org/10.1007/s00114-010-0674-y CrossRefPubMedGoogle Scholar
  56. Lewis CA (1981) Juvenile to adult shift in feeding strategies in the pedunculate barnacle Pollicipes Polymerus (Sowerby) (Cirripedia, Lepadomorpha). Crustaceana 41:14–20.  https://doi.org/10.1163/156854081x00039 CrossRefGoogle Scholar
  57. Lourey MJ, Trull TW, Sigman DM (2003) Sensitivity of δ15N of nitrate, surface suspended and deep sinking particulate nitrogen to seasonal nitrate depletion in the Southern Ocean. Glob Biogeochem Cycles 17:1081.  https://doi.org/10.1029/2002gb001973 CrossRefGoogle Scholar
  58. Lutjeharms JRE, Valentine HR (1984) Southern ocean thermal fronts south of Africa. Deep Sea Res Part Oceanogr Res Pap 31:1461–1475.  https://doi.org/10.1016/0198-0149(84)90082-7 CrossRefGoogle Scholar
  59. Luttikhuizen PC, Drent J, Van Delden W, Piersma T (2003) Spatially structured genetic variation in a broadcast spawning bivalve: quantitative vs. molecular traits. J Evol Biol 16:260–272.  https://doi.org/10.1046/j.1420-9101.2003.00510.x CrossRefPubMedGoogle Scholar
  60. McLeod R, Frew R, Hyndes G, Hurd C (2013) Unexpected shifts in fatty acid composition in response to diet in a common littoral amphipod. Mar Ecol Prog Ser 479:1–12CrossRefGoogle Scholar
  61. McQuaid CD, Froneman PW (2008) Biology in the oceanographic environment. The Prince Edward Islands: land–sea interactions in a changing ecosystem. Sun Press, Stellenbosh, pp 97–120CrossRefGoogle Scholar
  62. Miller RJ, Page HM (2012) Kelp as a trophic resource for marine suspension feeders: a review of isotope-based evidence. Mar Biol 159:1391–1402.  https://doi.org/10.1007/s00227-012-1929-2 CrossRefGoogle Scholar
  63. Miller RJ, Page HM, Reed DC (2015) Trophic versus structural effects of a marine foundation species, giant kelp (Macrocystis pyrifera). Oecologia.  https://doi.org/10.1007/s00442-015-3441-0 CrossRefPubMedGoogle Scholar
  64. Naddafi R, Rudstam LG (2013) Predator-induced behavioural defences in two competitive invasive species: the zebra mussel and the quagga mussel. Anim Behav 86:1275–1284.  https://doi.org/10.1016/j.anbehav.2013.09.032 CrossRefGoogle Scholar
  65. Nicastro KR, Zardi GI, McQuaid CD (2010) Differential reproductive investment, attachment strength and mortality of invasive and indigenous mussels across heterogeneous environments. Biol Invasions 12:2165–2177CrossRefGoogle Scholar
  66. Nikula R, Fraser C, Spencer H, Waters J (2010) Circumpolar dispersal by rafting in two subantarctic kelp-dwelling crustaceans. Mar Ecol Prog Ser 405:221–230.  https://doi.org/10.3354/meps08523 CrossRefGoogle Scholar
  67. Norkko J, Bonsdorff E, Norkko A (2000) Drifting algal mats as an alternative habitat for benthic invertebrates: species specific responses to a transient resource. J Exp Mar Biol Ecol 248:79–104.  https://doi.org/10.1016/s0022-0981(00)00155-6 CrossRefPubMedGoogle Scholar
  68. Nowlin WD, Whitworth T, Pillsbury RD (1977) Structure and transport of the Antarctic circumpolar current at Drake Passage from short-term measurements. J Phys Oceanogr 7:788–802.  https://doi.org/10.1175/1520-0485(1977)007%3c0788:satota%3e2.0.co;2 CrossRefGoogle Scholar
  69. O’Connor MI, Bruno JF, Gaines SD, Halpern BS, Lester SE, Kinlan BP, Weiss JM (2007) Temperature control of larval dispersal and the implications for marine ecology, evolution, and conservation. Proc Natl Acad Sci 104:1266–1271.  https://doi.org/10.1073/pnas.0603422104 CrossRefPubMedGoogle Scholar
  70. Orsi AH, Whitworth T III, Nowlin WD Jr (1995) On the meridional extent and fronts of the Antarctic circumpolar current. Deep Sea Res Part Oceanogr Res Pap 42:641–673.  https://doi.org/10.1016/0967-0637(95)00021-w CrossRefGoogle Scholar
  71. Öst M, Kilpi M (1997) A recent change in size distribution of blue mussels (Mytilus edulis) in the western part of the Gulf of Finland. Ann Zool Fenn 34:31–36Google Scholar
  72. Pakhomov EA, Froneman PW (1999) The Prince Edward Islands pelagic ecosystem, south Indian Ocean: a review of achievements, 1976–1990. J Mar Syst 18:355–367.  https://doi.org/10.1016/s0924-7963(97)00112-7 CrossRefGoogle Scholar
  73. Pakhomov E, Kaehler S, McQuaid C (2002) Zooplankton community structure in the kelp beds of the sub-Antarctic Prince Edward Archipelago: are they a refuge for larval stages? Polar Biol 25:778–788.  https://doi.org/10.1007/s00300-002-0411-x CrossRefGoogle Scholar
  74. Pakhomov EA, Ansorge IJ, Kaehler S, Vumazonke LU, Gulekana K, Bushula T, Balt C, Paul D, Hargey N, Stewart H, Chang N, Furno L, Mkatshwa S, Visser C, Lutjeharms JRE, Haynes-Foley P (2003) Studying the impact of ocean eddies on the ecosystem of the Prince Edward Islands: DEIMEC II. S Afr J Sci 99:187Google Scholar
  75. Parnell AC, Inger R, Bearhop S, Jackson AL (2010) Source partitioning using stable isotopes: coping with too nuch variation. PLoS One 5:e9672.  https://doi.org/10.1371/journal.pone.0009672 CrossRefPubMedPubMedCentralGoogle Scholar
  76. Parrish CC, Abrajano TA, Budge SM, Helleur RJ, Hudson ED, Pulchan K, Ramos C (2000) Lipid and phenolic biomarkers in marine ecosystems: analysis and applications. In: Wangersky PJ (ed) Marine chemistry. Springer, Berlin, pp 193–223CrossRefGoogle Scholar
  77. Perissinotto R, Duncombe Rae CM (1990) Occurrence of anticyclonic eddies on the Prince Edward Plateau (Southern Ocean): effects on phytoplankton biomass and production. Deep Sea Res Part Oceanogr Res Pap 37:777–793.  https://doi.org/10.1016/0198-0149(90)90006-h CrossRefGoogle Scholar
  78. Perissinotto R, Duncombe Rae C, Boden B, Allanson B (1990) Vertical stability as a controlling factor of the marine phytoplankton production at the Prince Edward Archipelago (Southern Ocean). Mar Ecol Prog Ser 60:205–209.  https://doi.org/10.3354/meps060205 CrossRefGoogle Scholar
  79. Perissinotto R, Lutjeharms JRE, van Ballegooyen RC (2000) Biological–physical interactions and pelagic productivity at the Prince Edward Islands, Southern Ocean. J Mar Syst 24:327–341.  https://doi.org/10.1016/s0924-7963(99)00093-7 CrossRefGoogle Scholar
  80. Pineda J, Hare JA, Sponaungle S (2007) Larval transport and dispersal in the coastal ocean and consequences for population connectivity. Oceanography 20(3):22–39.  https://doi.org/10.5670/oceanog.2007.27 CrossRefGoogle Scholar
  81. Porri F, Hill JM, McQuaid CD (2011) Associations in ephemeral systems: the lack of trophic relationships between sandhoppers and beach wrack. Mar Ecol Prog Ser 426:253–262.  https://doi.org/10.3354/meps08951 CrossRefGoogle Scholar
  82. Powell AWB (1979) New Zealand Mollusca: marine, land, and freshwater shells. Collins, New ZelandGoogle Scholar
  83. Puccinelli E, Noyon M, McQuaid CD (2016a) Does proximity to urban centres affect the dietary regime of marine benthic filter feeders? Estuar Coast Shelf Sci 169:147–157.  https://doi.org/10.1016/j.ecss.2015.12.017 CrossRefGoogle Scholar
  84. Puccinelli E, Noyon M, McQuaid CD (2016b) Hierarchical effects of biogeography and upwelling shape the dietary signatures of benthic filter feeders. Mar Ecol Prog Ser.  https://doi.org/10.3354/meps11567 CrossRefGoogle Scholar
  85. Puccinelli E, McQuaid CD, Noyon M (2016c) Spatio-temporal variation in effects of upwelling on the fatty acid composition of benthic filter feeders in the Southern Benguela ecosystem: not all upwelling Is equal. PLoS One 11:e0161919.  https://doi.org/10.1371/journal.pone.0161919 CrossRefPubMedPubMedCentralGoogle Scholar
  86. Puccinelli E, McQuaid CD, Ansorge IJ (2018) Factors affecting trophic compositions of offshore benthic invertebrates at a sub-Antarctic archipelago. Limnol Oceanogr 11:e0161919.  https://doi.org/10.1002/lno.10934 CrossRefGoogle Scholar
  87. Rau G, Teyssie J-L, Rassoulzadegan F, Fowler S (1990) 13C/12C and 15 N/14 N variations among size-fractionated marine particles: implications for their origin and trophic relationships. Mar Ecol Prog Ser 59:33–38.  https://doi.org/10.3354/meps059033 CrossRefGoogle Scholar
  88. Rossi F, Herman PMJ, Middelburg JJ (2004) Interspecific and intraspecific variation of δC and δN in deposit- and suspension-feeding bivalves (Macoma balthica and Cerastoderma edule): evidence of ontogenetic changes in feeding mode of Macoma balthica. Limnol Oceanogr 49:408–414.  https://doi.org/10.4319/lo.2004.49.2.0408 CrossRefGoogle Scholar
  89. Schapira M, McQuaid CD, Froneman PW (2012) Free-living and particle-associated prokaryote metabolism in giant kelp forests: implications for carbon flux in a sub-Antarctic coastal area. Estuar Coast Shelf Sci 106:69–79.  https://doi.org/10.1016/j.ecss.2012.04.031 CrossRefGoogle Scholar
  90. Scheltema RS (1988) Initial evidence for the transport of teleplanic larvae of benthic invertebrates across the East Pacific Barrier. Biol Bull 174:145–152.  https://doi.org/10.2307/1541781 CrossRefGoogle Scholar
  91. Schlechtriem C, Arts MT, Johannsson OE (2008) Effect of long-term fasting on the use of fatty acids as trophic markers in the opossum shrimp Mysis relicta—a laboratory study. J Gt Lakes Res 34:143–152.  https://doi.org/10.3394/0380-1330(2008)34%5b143:eolfot%5d2.0.co;2 CrossRefGoogle Scholar
  92. Sieburth JM, Smetacek V, Lenz J (1978) Pelagic ecosystem structure: heterotrophic compartments of the plankton and their relationship to plankton size fractions. Limnol Oceanogr 23:1256–1263.  https://doi.org/10.4319/lo.1978.23.6.1256 CrossRefGoogle Scholar
  93. Silva ACF, Hawkins SJ, Boaventura DM, Thompson RC (2008) Predation by small mobile aquatic predators regulates populations of the intertidal limpet Patella vulgata (L.). J Exp Mar Biol Ecol 367:259–265.  https://doi.org/10.1016/j.jembe.2008.10.010 CrossRefGoogle Scholar
  94. Smith SDA (2002) Kelp rafts in the Southern Ocean. Glob Ecol Biogeogr 11:67–69.  https://doi.org/10.1046/j.1466-822x.2001.00259.x CrossRefGoogle Scholar
  95. Soares MA, Bhaskar PV, Naik RK, Dessai D, George J, Tiwari M, Anilkumar N (2015) Latitudinal δ13C and δ15N variations in particulate organic matter (POM) in surface waters from the Indian ocean sector of Southern Ocean and the Tropical Indian Ocean in 2012. Deep Sea Res Part II Top Stud Oceanogr 118 Part B:186–196.  https://doi.org/10.1016/j.dsr2.2015.06.009 CrossRefGoogle Scholar
  96. Tieszen LL, Boutton TW, Tesdahl KG, Slade NA (1983) Fractionation and turnover of stable carbon isotopes in animal tissues: implications for δ13C analysis of diet. Oecologia 57:32–37.  https://doi.org/10.1007/bf00379558 CrossRefPubMedGoogle Scholar
  97. Tzetlin AB, Mokievsky VO, Melnikov AN, Saphonov MV, Simdyanov TG, Ivanov IE (1997) Fauna associated with detached kelp in different types of subtidal habitats of the White Sea. Hydrobiologia 355:91–100.  https://doi.org/10.1023/a:1003098616811 CrossRefGoogle Scholar
  98. Vandendriessche S, Stienen EWM, Vincx M, Degraer S (2007) Seabirds foraging at floating seaweeds in the Northeast Atlantic. Ardea 95:289–298.  https://doi.org/10.5253/078.095.0211 CrossRefGoogle Scholar
  99. von der Meden CEO, Cole VJ, McQuaid CD (2015) Do the threats of predation and competition alter larval behaviour and selectivity at settlement under field conditions? J Exp Mar Biol Ecol 471:240–246.  https://doi.org/10.1016/j.jembe.2015.06.017 CrossRefGoogle Scholar
  100. von der Meden CEO, Atkinson LJ, Branch GM, Asdar S, Ansorge IJ, van den Berg M (2017) Long-term change in epibenthic assemblages at the Prince Edward Islands: a comparison between 1988 and 2013. Polar Biol.  https://doi.org/10.1007/s00300-017-2132-1 CrossRefGoogle Scholar
  101. Wada E, Hattori A (1978) Nitrogen isotope effects in the assimilation of inorganic nitrogenous compounds by marine diatoms. Geomicrobiol J 1:85–101.  https://doi.org/10.1080/01490457809377725 CrossRefGoogle Scholar
  102. Wakeham SG, Beier JA (1991) Fatty acid and sterol biomarkers as indicators of particulate matter source and alteration processes in the Black Sea. Deep Sea Res Part A 38:943–968.  https://doi.org/10.1016/s0198-0149(10)80018-4 CrossRefGoogle Scholar
  103. Ward EJ, Shumway SE (2004) Separating the grain from the chaff: particle selection in suspension- and deposit-feeding bivalves. J Exp Mar Biol Ecol 300:83–130.  https://doi.org/10.1016/j.jembe.2004.03.002 CrossRefGoogle Scholar
  104. Weersing K, Toonen RJ (2009) Population genetics, larval dispersal, and connectivity in marine systems. Mar Ecol Prog Ser 393:1–12CrossRefGoogle Scholar
  105. Worcester SE (1994) Adult rafting versus larval swimming: dispersal and recruitment of a botryllid ascidian on eelgrass. Mar Biol 121:309–317.  https://doi.org/10.1007/bf00346739 CrossRefGoogle Scholar
  106. Wright SW, Thomas DP, Marchant HJ, Higgins HW, Mackey MD, Mackey DJ (1996) Analysis of phytoplankton of the Australian sector of the Southern Ocean: comparisons of microscopy and size frequency data with interpretations of pigment HPLC data using the “CHEMTAX” matrix factorisation program. Mar Ecol Prog Ser 144:285–298CrossRefGoogle Scholar
  107. York JK, Tomasky G, Valiela I, Repeta DJ (2007) Stable isotopic detection of ammonium and nitrate assimilation by phytoplankton in the Waquoit Bay estuarine system. Limnol Oceanogr 52:144–155.  https://doi.org/10.4319/lo.2007.52.1.0144 CrossRefGoogle Scholar
  108. Zanden MJV, Rasmussen JB (1999) Primary consumer δ13C and δ15N and the trophic position of aquatic consumers. Ecology 80:1395–1404. https://doi.org/10.1890/0012-9658(1999)080[1395:pccana]2.0.co;2CrossRefGoogle Scholar
  109. Zardi GI, McQuaid CD, Nicastro KR (2007) Balancing survival and reproduction: seasonality of wave action, attachment strength and reproductive output in indigenous Perna perna and invasive Mytilus galloprovincialis mussels. Mar Ecol Prog Ser 334:155–163.  https://doi.org/10.3354/meps334155 CrossRefGoogle Scholar
  110. Zelaya DG (2005) The bivalves from the Scotia Arc islands: species richness and faunistic affinities. Sci Mar 69:113–122.  https://doi.org/10.3989/scimar.2005.69s2113 CrossRefGoogle Scholar

Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of Oceanography, Marine Research InstituteUniversity of Cape TownCape TownSouth Africa
  2. 2.South African Environmental Observation Network (SAEON)Cape TownSouth Africa
  3. 3.Department of Zoology and EntomologyRhodes UniversityGrahamstownSouth Africa

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