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Isotopic Composition of Middle Old Red Sandstone Carbonates: Implications for the Palaeoenvironment


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1 Department of Geology and Applied Geology, University of Glasgow, Glasgow G12 8QQ, Scotland, United Kingdom
     

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The carbonates occurring within the sandstones of the Middle Old Red Sandstone of the Orcadian basin (Middle Devonian) in Caithness, N.E. Scotland are of minor abundance, predominantly calcite and may be petrographically ascribed to early diagenetic origin.

Isotopic analyses (C, O, Sr) have been undertaken to elucidate the depositional mileu of these carbonates at two localities, Wick and Reay. Calcite and dolomite coexist in carbonate facies rocks and their similarity in δ13CPDB (-4.57 ± 0.64 and -4.56 ± 0.53‰ respectively at Wick and -2.39 ± 0.30 and -2.00 ± 0.48 respectively at Reay) suggest a cogenetic origin at each locality. The δ13C values also suggest deposition from lighter, freshwater.

Mean calcite δ18OPDB values of -7.76 ± 1.92‰ and -8.76 ± 2.23‰ for Wick and Reay samples respectively also support this contention. Dolomite δ18OPDB values are consistently heavier which is not inconsistent with a generally cogenetic origin. The oxygen isotope data reflects a lighter pore fluid composition either because of diagenetic modification by carbonate recrystallization or a greater contribution of freshwater via river supply during sandstone deposition in an ephemerally evaporative lacustrine environment. Mean Sr87/86 value of 0.711167 for the carbonates of Wick confinn a nonmarine origin.


Keywords

Isotope Geochemistry, O, C and Sr Isotopes, Cogenetic Calcite and Dolomite, Orcadian, Lacustrine, Freshwater.
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  • Isotopic Composition of Middle Old Red Sandstone Carbonates: Implications for the Palaeoenvironment

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Authors

Nachiketa Das
Department of Geology and Applied Geology, University of Glasgow, Glasgow G12 8QQ, Scotland, United Kingdom

Abstract


The carbonates occurring within the sandstones of the Middle Old Red Sandstone of the Orcadian basin (Middle Devonian) in Caithness, N.E. Scotland are of minor abundance, predominantly calcite and may be petrographically ascribed to early diagenetic origin.

Isotopic analyses (C, O, Sr) have been undertaken to elucidate the depositional mileu of these carbonates at two localities, Wick and Reay. Calcite and dolomite coexist in carbonate facies rocks and their similarity in δ13CPDB (-4.57 ± 0.64 and -4.56 ± 0.53‰ respectively at Wick and -2.39 ± 0.30 and -2.00 ± 0.48 respectively at Reay) suggest a cogenetic origin at each locality. The δ13C values also suggest deposition from lighter, freshwater.

Mean calcite δ18OPDB values of -7.76 ± 1.92‰ and -8.76 ± 2.23‰ for Wick and Reay samples respectively also support this contention. Dolomite δ18OPDB values are consistently heavier which is not inconsistent with a generally cogenetic origin. The oxygen isotope data reflects a lighter pore fluid composition either because of diagenetic modification by carbonate recrystallization or a greater contribution of freshwater via river supply during sandstone deposition in an ephemerally evaporative lacustrine environment. Mean Sr87/86 value of 0.711167 for the carbonates of Wick confinn a nonmarine origin.


Keywords


Isotope Geochemistry, O, C and Sr Isotopes, Cogenetic Calcite and Dolomite, Orcadian, Lacustrine, Freshwater.