Hostname: page-component-cd9895bd7-gbm5v Total loading time: 0 Render date: 2024-12-23T01:17:47.018Z Has data issue: false hasContentIssue false

Controls, variation, and a record of climate change in detailed stable isotope record in a single bryozoan skeleton

Published online by Cambridge University Press:  20 January 2017

Abigail M. Smith*
Affiliation:
Department of Marine Science, University of Otago, P. O. Box 56, Dunedin, New Zealand
Marcus M. Key Jr.
Affiliation:
Department of Geology, Dickinson College, Carlisle, PA 17013-2896, USA
*
*Corresponding author. Fax: +1-64-3-479-8336.E-mail address:[email protected] (A.M. Smith).

Abstract

The long-lived (about 20 yr) bryozoan Adeonellopsis sp. from Doubtful Sound, New Zealand, precipitates aragonite in isotopic equilibrium with seawater, exerting no metabolic or kinetic effects. Oxygen isotope ratios (δ18O) in 61 subsamples (along three branches of a single unaltered colony) range from −0.09 to +0.68‰ PDB (mean = +0.36‰ PDB). Carbon isotope ratios (δ13C) range from +0.84 to +2.18‰ PDB (mean = +1.69‰ PDB). Typical of cool-water carbonates, δ18O-derived water temperatures range from 14.2 to 17.5 °C. Adeonellopsis has a minimum temperature growth threshold of 14 °C, recording only a partial record of environmental variation. By correlating seawater temperatures derived from δ18O with the Southern Oscillation Index, however, we were able to detect major events such as the 1983 El Niño. Interannual climatic variation can be recorded in skeletal carbonate isotopes. The range of within-colony isotopic variability found in this study (0.77‰ in δ18O and 1.34 in δ13C) means that among-colony variation must be treated cautiously. Temperate bryozoan isotopes have been tested in less than 2% of described extant species — this highly variable phylum is not yet fully understood.

Type
Research Article
Copyright
University of Washington

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

Supplementary data for this article (Appendix) are available on Science Direct (http://www.sciencedirect.com).

References

Amini, Z.Z., Rao, C.P., (1998). Depth and latitudinal characteristics of sedimentological and geochemical variables in temperate shelf carbonates, eastern Tasmania, Australia. Carbonates and Evaporites. 13, 145156.Google Scholar
Bader, B., (2000). Life cycle, growth rate, and carbonate production of Cellaria sinuosa . Herrera Cubilla, A., Jackson, J.B.C., Proceedings of the 11th International Bryozoology Association Conference, Smithsonian Tropical Research Institute, Balboa. 136144.Google Scholar
Barnes, D.K.A., (1995). Seasonal and annual growth in erect species of Antarctic bryozoans. Journal of Experimental Marine Biology and Ecology. 188, 181198.Google Scholar
Bemis, B.E., Geary, D.H., (1996). The usefulness of bivalve stable isotope profiles as environmental indicators: data from the eastern Pacific Ocean and the southern Caribbean Sea. Palaios. 11, 328339.Google Scholar
Bone, Y., James, N.P., (1993). Bryozoans as carbonate sediment producers on the cool-water Lacepede shelf, southern Australia. Sedimentary Geology. 86, 247271.Google Scholar
Bone, Y., James, N.P., (1996). Stable isotopes: do all cool-water bryozoans equally reflect the same parameters?. Geological Society of Australia(Abstracts No. 41, 48).Google Scholar
Bone, Y., James, N.P., (1997). Bryozoan stable isotope survey from the cool-water Lacepede Shelf, Southern Australia. James, N.P, Clarke, J.A.D., Cool-Water Carbonates. SEPM Special Publication. vol. 56, 93106.Google Scholar
Brey, T., Gerdes, D., Gutt, J., MacKensen, A., Starmans, A., (1999). Growth and age of the Antarctic bryozoan Cellaria incula on the Weddell Sea Shelf. Antarctic Science. 11, 408414.Google Scholar
Cocito, S., Ferdeghini, F., (2001). Carbonate standing stock and carbonate production of the bryozoan Pentapora fascialis in the north-western Mediterranean. Facies. 45, 2530.Google Scholar
Corfield, R.M., (1995). An introduction to the techniques, limitations and landmarks of carbonate oxygen isotope palaeothermometry. Bosence, D.W.J., Allison, P.A., Marine Palaeoenvironmental Analysis from Fossils. Geological Society Special Publication. vol. 83, The Geological Society, London., 2743.Google Scholar
Crowley, S.F., Taylor, P.D., (2000). Stable isotope composition of modern bryozoan skeletal carbonate from the Otago Shelf, New Zealand. New Zealand Journal of Marine and Freshwater Research. 34, 331351.CrossRefGoogle Scholar
Forester, R.M., Sandberg, P.A., Anderson, T.F., (1973). Isotopic variability of cheilostome bryozoan skeletons. Larwood, G.P., Living and Fossil Bryozoa: Recent Advances in Research. Academic Press, 7994.Google Scholar
Gibbs, M.T., Bowman, M.J., Dietrich, D.E., (2000). Maintenance of near-surface stratification in Doubtful Sound, a New Zealand fjord. Estuarine, Coastal and Shelf Science. 51, 683704.Google Scholar
Goodwin, D.H., Flessa, K.W., Schöne, B.R., Dettman, D.L., (2001). Cross-calibration of daily growth increments, stable isotope variation, and temperature in the Gulf of California bivalve mollusk Chione cortezi: implications for paleoenvironmental analysis. Palaios. 16, 387398.Google Scholar
Goodwin, D.H., Flessa, K.W., Schöne, B.R., Dettman, D.L., (2003). Resolution and fidelity of oxygen isotopes as paleotemperature proxies in bivalve mollusk shells: models and observations. Palaios. 18, 110125.Google Scholar
Grossman, E.L., Ku, T.-L., (1986). Oxygen and carbon isotope fractionation in biogenic aragonite: temperature effects. Chemical Geology. 59, 5974.Google Scholar
James, N.P., (1997). The cool-water carbonate depositional realm. James, N.P, Clarke, J.A.D., Cool-Water Carbonates. SEPM Special Publication. 56, 120.Google Scholar
Jamet, C., (1999). Bryozoan colony growth rates: a proxy for cool-water marine carbonate production rates. Senior Independent research report, Dickinson College, Spring., 41 pp.Google Scholar
Jones, D.S., Quitmyer, I.R., (1996). Marking time with bivalve shells: oxygen isotopes and season of annual increment formation. Palaios. 11, 340346.Google Scholar
Keeling, C.D., (1979). Recent trends in the 13C/12C ratio of atmospheric carbon dioxide. Nature. 277, 121122.Google Scholar
Kyser, T.K., James, N.P., Bone, Y., (1998). Alteration of Cenozoic cool-water carbonates to low-Mg calcite in marine waters, Gambier Embayment, South Australia. Journal of Sedimentary Research. 68, 947955.Google Scholar
Lamare, M., (1997). Recruitment processes and Larval Biology of Evechinus chloroticus in Doubtful Sound and Marlborough Sound, New Zealand. Ph.D. dissertation, University of Otago, Dunedin, New Zealand.Google Scholar
Lamare, M.D., Brewin, P.E., Barker, M.F., Wing, S.R., (2002). Reproduction of the sea urchin Evechinus chloroticus (Echinodermata: Echinoidea) in a New Zealand fiord. New Zealand Journal of Marine and Freshwater Research. 36, 719732.Google Scholar
Lidgard, S., Buckley, G.A., (1994). Toward a morphological species concept in cheilostomates: phenotypic variation in Adeonellopsis yarraensis (Waters). Hayward, P.J., Ryland, J.S., Taylor, P.D., Biology and Palaeobiology of Bryozoans. Proceedings of the 9th International Bryozoology ConferenceOlsen & Olsen, Fredensborg., 101105.Google Scholar
Machiyama, H., Yamada, T., Kaneko, N., Iryu, Y., Odawara, K., Asami, R., Matsuda, H., Mawatari, S.F., Bone, Y., James, N.P., (2003). Carbon and oxygen isotopes of cool-water bryozoans from the Great Australian Bight and their paleoenvironmental significance. Hine, A.C., Feary, D.A., Malone, M.J., Proceedings of the Ocean Drilling Program. Scientific Results. vol. 182, 129.Google Scholar
Macrellis, H.M., (2001). The Littleneck Clams that couldn't — the New Zealand Littleneck Clam (Austrovenus stutchburyi) population in Doubtful Sound and the role of the Manapouri power plant in influencing clam distribution. MSc thesis, Marine Science, University of Otago, Dunedin, New Zealand., January 2001.Google Scholar
Nelson, C.S., Smith, A.M., (1996). Stable oxygen and carbon isotope compositional fields for skeletal and diagenetic components in New Zealand Cenozoic nontropical carbonate sediments and limestones: a synthesis and review. New Zealand Journal of Geology and Geophysics. 39, 93107.Google Scholar
Nelson, C.S., Keane, S.L., Head, P.S., (1988). Non-tropical carbonate deposits on the modern New Zealand shelf. Sedimentary Geology. 60, 7194.Google Scholar
Pätzold, J., Ristedt, H., Wefer, G., (1987). Rate of growth and longevity of a large colony of Pentapora foliacea (Bryozoa) recorded in their oxygen isotope profiles. Marine Biology. 96, 535538.Google Scholar
Peake, B.M., Walls, D.J., Gibbs, M.T., (2001). Spatial variations in the levels of nutrients, chlorophyll a, and dissolved oxygen in summer and winter in Doubtful Sound, New Zealand. New Zealand Journal of Marine and Freshwater Research. 35, 681694.Google Scholar
Purton, L.M.A., Brasier, M.D., (1999). Giant protist Nummulites and its Eocene environment: lifespan and habitat insights from δ18O and δ13C from Nummulites and Venericardia, Hampshire Basin, UK. Geology. 27, 711714.Google Scholar
Queensland Department of Natural Resources and Mines, (2003). http://www.longpaddock.qld.gov.au/SeasonalClimateOutlook/SouthernOscillationIndex/.Google Scholar
Rahimpour-Bonab, H., Bone, Y., Moussavi-Harami, R., (1997a). Stable isotope aspects of modern molluscs, brachiopods, and marine cements from cool-water carbonates, Lacepede Shelf, South Australia. Geochemica et Cosmochemica Acta. 61, 207218.CrossRefGoogle Scholar
Rahimpour-Bonab, H., Bone, Y., Moussavi-Harami, R., Turnbull, K., (1997b). Geochemical comparison of modern cool-water calcareous biota, Lacepede Shelf, South Australia, with their tropical counterparts. James, N.P, Clarke, J.A.D., Cool-Water Carbonates. SEPM Special Publication. vol. 56, 7791.Google Scholar
Rao, C.P., (1996). Oxygen and carbon isotope composition of skeletons from temperate shelf carbonates, eastern Tasmania, Australia. Carbonates and Evaporites. 11, 169181.Google Scholar
Rao, C.P., Nelson, C.S., (1992). Oxygen and carbon isotope fields for temperate shelf carbonates from Tasmania and New Zealand. Marine Geology. 103, 273286.Google Scholar
Romanek, C.S., Grossman, E.T., Morse, J.W., (1992). Carbonate isotope fractionation in synthetic aragonite and calcite: effects of temperature and precipitation rate. Geochimica et Cosmochimica Acta. 56, 419430.Google Scholar
Ryland, J.S., (1976). Physiology and ecology of marine bryozoans. Advances in Marine Biology. 14, 285443.CrossRefGoogle Scholar
Smith, A.M., Nelson, C.S., Spencer, H.G., (1998). Skeletal mineralogy of New Zealand bryozoans. Marine Geology. 151, 2746.Google Scholar
Smith, A.M., Stewart, B., Key, M.M. Jr., Jamet, C.M., (2001). Growth and carbonate production by Adeonellopsis (Bryozoa: Cheilostomata) in Doubtful Sound, New Zealand. Palaeogeography, Palaeoclimatology, Palaeoecology. 175, 201210.Google Scholar
Stebbing, A.R.D., (1971). The epizoic fauna of Flustra foliacea (Bryozoa). Journal of Marine Biological Association of the United Kingdom. 28, 227234.Google Scholar
Swart, P.K., Dodge, R.E., Hudson, H.J., (1996). A 240-year stable oxygen and carbon isotopic record in a coral from south Florida: implications for the prediction of precipitation in southern Florida. Palaios. 11, 362375.Google Scholar
Tarutani, T., Clayton, R.N., Mayeda, T., (1969). The effects of polymorphism and magnesium substitution on oxygen isotope fractionation between calcium carbonate and water. Geochimica et Cosmochimica Acta. 33, 987996.Google Scholar
Supplementary material: File

Smith and Key Supplementary Material

Supplementary Material

Download Smith and Key Supplementary Material(File)
File 53.2 KB