Calcite sea

From Wikipedia, the free encyclopedia
  (Redirected from Calcite seas)
Jump to: navigation, search
The alternation of calcite and aragonite seas through geologic time.

A calcite sea is one in which low-magnesium calcite is the primary inorganic marine calcium carbonate precipitate. An aragonite sea is the alternate seawater chemistry in which aragonite and high-magnesium calcite are the primary inorganic carbonate precipitates. The Early Paleozoic and the Middle to Late Mesozoic oceans were predominantly calcite seas, whereas the Middle Paleozoic through the Early Mesozoic and the Cenozoic (including today) are characterized by aragonite seas (Wilkinson et al., 1985; Wilkinson and Given, 1986; Morse and Mackenzie, 1990; Lowenstein et al., 2001; Palmer and Wilson, 2004).

Jurassic hardground with encrusting oysters and borings.

The most significant geological and biological effects of calcite sea conditions include rapid and widespread formation of carbonate hardgrounds (Palmer, 1982; Palmer et al., 1988; Wilson and Palmer, 1992), calcitic ooids (Sandberg, 1983; Wilkinson et al., 1985), calcite cements (Wilkinson and Given, 1986), and the contemporaneous dissolution of aragonite shells in shallow warm seas (Cherns and Wright, 2000; Palmer and Wilson, 2004). Hardgrounds were very common, for example, in the calcite seas of the Ordovician and Jurassic, but virtually absent from the aragonite seas of the Permian (Palmer, 1982).

Fossils of invertebrate organisms found in calcite sea deposits are usually dominated by either thick calcite shells and skeletons (Wilkinson, 1979; Stanley and Hardie, 1998, 1999; Porter, 2007), were infaunal and/or had thick periostraca (Pojeta, 1971), or had an inner shell of aragonite and an outer shell of calcite (Harper et al., 1997). This was apparently because aragonite dissolved quickly on the seafloor and had to be either avoided or protected as a biomineral (Palmer and Wilson, 2004).

Calcite seas were coincident with times of rapid seafloor spreading and global greenhouse climate conditions (Stanley and Hardie, 1999). Seafloor spreading centers cycle seawater through hydrothermal vents, reducing the ratio of magnesium to calcium in the seawater through metamorphism of calcium-rich minerals in basalt to magnesium-rich clays (Wilkinson and Given, 1986; Lowenstein et al., 2001). This reduction in the Mg/Ca ratio favors the precipitation of calcite over aragonite. Increased seafloor spreading also means increased volcanism and elevated levels of carbon dioxide in the atmosphere and oceans. This may also have an effect on which polymorph of calcium carbonate is precipitated (Lowenstein et al., 2001).

References[edit]

  • Cherns, L., Wright, V.P. (2000). "Missing molluscs as evidence of large-scale, early skeletal aragonite dissolution in a Silurian Sea". Geology 28 (9): 791–794. Bibcode:2000Geo....28..791C. doi:10.1130/0091-7613(2000)28<791:MMAEOL>2.0.CO;2. 
  • Harper, E.M., Palmer, T.J., Alphey, J.R. (1997). "Evolutionary response by bivalves to changing Phanerozoic sea-water chemistry". Geological Magazine 134 (3): 403–407. doi:10.1017/S0016756897007061. 
  • Lowenstein, T.K., Timofeeff, M.N., Brennan, S.T., Hardie, L.A., Demicco, R.V. (2001). "Oscillations in Phanerozoic seawater chemistry: evidence from fluid inclusions". Science 294 (5544): 1086–1088. Bibcode:2001Sci...294.1086L. doi:10.1126/science.1064280. PMID 11691988. 
  • Morse, J.W., Mackenzie, F.T. (1990). "Geochemistry of sedimentary carbonates". Developments in Sedimentology 48: 1–707. doi:10.1016/S0070-4571(08)70330-3. 
  • Palmer, T.J., Wilson, M.A. (2004). "Calcite precipitation and dissolution of biogenic aragonite in shallow Ordovician calcite seas". Lethaia 37 (4): 417–427[1]. doi:10.1080/00241160410002135. 
  • Palmer, T.J. (1982). "Cambrian to Cretaceous changes in hardground communities". Lethaia 15 (4): 309–323. doi:10.1111/j.1502-3931.1982.tb01696.x. 
  • Palmer, T.J., Hudson, J.D., Wilson, M.A. (1988). "Palaeoecological evidence for early aragonite dissolution in ancient calcite seas". Nature 335 (6193): 809–810. Bibcode:1988Natur.335..809P. doi:10.1038/335809a0. 
  • Pojeta, J., Jr. (1988). "Review of Ordovician pelecypods". U.S. Geological Survey Professional Paper 1044: 1–46. 
  • Porter, S.M. (2007). "Seawater chemistry and early carbonate biomineralization". Science 316 (5829): 1302–1304. Bibcode:2007Sci...316.1302P. doi:10.1126/science.1137284. PMID 17540895. 
  • Sandberg, P.A. (1983). "An oscillating trend in Phanerozoic non-skeletal carbonate mineralogy". Nature 305 (5929): 19–22. Bibcode:1983Natur.305...19S. doi:10.1038/305019a0. 
  • Stanley, S.M., Hardie, L.A. (1998). "Secular oscillations in the carbonate mineralogy of reef-building and sediment-producing organisms driven by tectonically forced shifts in seawater chemistry". Palaeogeography, Palaeoclimatology, Palaeoecology 144 (1-2): 3–19. doi:10.1016/S0031-0182(98)00109-6. 
  • Stanley, S.M., Hardie, L.A. (1999). "Hypercalcification; paleontology links plate tectonics and geochemistry to sedimentology". GSA Today 9: 1–7. 
  • Wilkinson, B.H. (1979). "Biomineralization, paleooceanography, and the evolution of calcareous marine organisms". Geology 7 (11): 524–527. Bibcode:1979Geo.....7..524W. doi:10.1130/0091-7613(1979)7<524:BPATEO>2.0.CO;2. 
  • Wilkinson, B.H., Given, K.R. (1986). "Secular variation in abiotic marine carbonates: constraints on Phanerozoic atmospheric carbon dioxide contents and oceanic Mg/Ca ratios". Journal of Geology 94 (3): 321–333. Bibcode:1986JG.....94..321W. doi:10.1086/629032. 
  • Wilkinson, B.H., Owen, R.M., Carroll, A.R. (1985). "Submarine hydrothermal weathering, global eustacy, and carbonate polymorphism in Phanerozoic marine oolites". Journal of Sedimentary Petrology 55: 171–183. 
  • Wilson, M.A., Palmer, T.J. (1992). "Hardgrounds and hardground faunas". University of Wales, Aberystwyth, Institute of Earth Studies Publications 9: 1–131.