Summary
The hypothesis that relative water motion and boundary layer diffusion processes affect carbon isotope ratios of aquatic plants was tested in tidal pool and surge zone comparisons of the surfgrass Phyllospadix spp. No evidence was found that submerged plants growing in still upper tidal pools were isotopically different from those growing submerged in lower tidal surge zones. Significant decreases in 13C/12C ratios for plants growing emersed in the intertidal may have been caused by uptake of atmospheric carbon dioxide. Marine algae (Egregia menziesii and Halosaccion americanum) growing at the same location and tidal elevations as the seagrasses showed somewhat different isotopic fractionation patterns, suggesting that causes of isotopic variability in the seagrasses were not necessarily the same as those in the two marine algae.
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References
Barbour MG, Radosevich SR (1979) 14C uptake by the marine angiosperm Phyllospadix scouleri. Am J Bot 66:301–306
Beer S, Waisel Y (1979) Some photosynthetic carbon fixation properties of seagrasses. Aquat Bot 31:1019–1026
Beer S, Eshel A, Waisel Y (1977) Carbon metabolism in seagrasses. I. The utilization of exogenous inorganic carbon species in photosynthesis. J Exp Bot 28:1180–1189
Broecker WS (1982) Tracers in the sea. Lamont-Doherty Geological Laboratory. Palisades, NY
Conover JT (1968) The importance of natural diffusion gradients and transport of substances related to benthic marine plant metabolism. Bot Mar 11:1–9
Craig H (1953) The geochemistry of the stable carbon isotopes. Geochim Cosmochim Acta 3:53–92
Craig H (1957) Isotopic standards for carbon and oxygen and correction factors for mass spectrometric analysis of carbon dioxide. Geochim Cosmochim Acta 12:133–149
den Hartog C (1970) The seagrasses of the world. Elsevier/North-Holland, Amsterdam
Deuser WG, Degens ET (1967) Carbon isotope fractionation in the system CO2(gas)-CO2(aqeuous)-HCO3-(aqueous). Nature 215:1033–1035
Drumgoole FI (1978) The effect of oxygen and dark respiration and apparent photosynthesis of marine macro-algae. Aquat Bot 4:281–297
Dunton K, Schell DM (1987) Dependence of consumers on macroalgal (Laminaria solundgula) carbon in an arctic kelp community: δ13C evidence. Mar Biol 93:615–625
Faganeli J, Vukovic A, Saleh FI, Pezdic J (1986) C:N:P ratios and stable carbon and hydrogen isotopes in the benthic marine algae, Ulva rigida C. Ag. and Fucus virsoides. J. Ag. J Exp Mar Biol Ecol 102:153–166
Galimov EM (1985) The biological fractionation of isotopes. Academic Press, Orlando
Millhouse J, Strother S (1986) The effect of pH on the inorganic carbon source for photosynthesis in the seagrass Zostera muelleri Irmisch. ex. Aschers. Aquat Bot 24:199–209
Mook WG, Bommerson JC, Stavermann WH (1974) Carbon isotope fractionation between dissolved bicarbonate and gaseous carbon dioxide. Earth Planet Sci Lett 22:169–175
Morris S, Taylor AC (1983) Diurnal and seasonal variation in physico-chemical conditions within intertidal rock pools. Estuarine Coastal Shelf Sci 17:339–357
Oates B (1986) Components of photosynthesis in the intertidal saccate alga Halosaccion americanum (Rhodophyta, Palmariales). J Phycol 22:217–223
Osmond CB, Valaane N, Haslam SM, Uotila P, Roksandic Z (1981) Comparisons of δ13C in leaves of aquatic macrophytes from different habitats in Britain and Finland; some implications for photosynthetic processes in aquatic plants. Oecologia (Berlin) 50:117–124
Parker PL, Calder JA (1970) Stable carbon isotope ratio variations in biological systems. In: Hood DW (ed) Organic matter in natural waters. Inst. of Marine Science, Occasional Publication No. 1, University of Alaska, Fairbanks
Park R, Epstein S (1960) Carbon isotope fractionation during photosynthesis. Geochim Cosmochim Acta 21:110–126
Phillips RC (1979) Ecological notes on Phyllospadix (Potamogetonaceae) in the northeast Pacific. Aquat Bot 6:159–170
Raven JA (1970) Exogenous inorganic carbon sources in plant photosynthesis. Biol Rev 45:167–221
Raven JA (1981) Nutritional strategies of submerged benthic plants: the acquisition of C, N and P by rhizophytes and haptophytes. New Phytol 88:1–30
Raven JA, Beardall J, Griffiths H (1982) Inorganic C-sources for Lemanea, Cladophora and Ranunculus in a fast-flowing stream: measurements of gas exchange and of carbon isotope ratios and their ecological implications. Oecologia (Berlin) 53:68–78
Smith FA, Walker NA (1980) Photosynthesis by aquatic plants: effects of unstirred layers in relation to assimilation of CO2 and HCO -3 and to carbon isotopic discrimination. New Phytol 86:245–259
Steeman-Nielsen E (1975) Marine photosynthesis. Elsevier Scientific, Amsterdam
Stephenson RL, Tan FC, Mann KH (1984) Stable carbon isotope variability in marine macrophytes and its implications for food web studies. Mar Biol 81:223–230
Thode HG, Shima KH, Rees CE, Krishnamurty KV (1965) Carbon-13 isotope effects in systems containing carbon dioxide, bicarbonate, carbonate, and metal ions. Can J Chem 43:582–595
Truchot J-P, Duhamel-Jouve A (1980) Oxygen and carbon dioxide in the marine intertidal environment: diurnal and tidal changes in rockpools. Respir Physiol 39:241–254
Wendt I (1968) Fractionation of carbon isotopes and its temperature dependence in the system CO2-gas-CO2 in solution and HCO3−CO2 in solution. Earth Planet Sci Lett 4:64–68
Wheeler WN (1980) Effect of boundary layer transport on the fixation of carbon by the giant kelp Macrocystis pyriferd. Mar Biol 56:103–110
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Cooper, L.W., McRoy, C.P. Stable carbon isotope ratio variations in marine macrophytes along intertidal gradients. Oecologia 77, 238–241 (1988). https://doi.org/10.1007/BF00379192
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DOI: https://doi.org/10.1007/BF00379192