TY - JOUR
T1 - P/Ca in Carbonates as a Proxy for Alkalinity and Phosphate Levels
AU - Ingalls, Miquela
AU - Blättler, Clara L.
AU - Higgins, John A.
AU - Magyar, John S.
AU - Eiler, John M.
AU - Fischer, Woodward W.
N1 - Publisher Copyright:
©2020. American Geophysical Union. All Rights Reserved.
PY - 2020/11/16
Y1 - 2020/11/16
N2 - Understanding mechanisms, rates, and drivers of past carbonate formation provides insight into the chemical evolution of Earth's oceans and atmosphere. We paired geological observations with elemental and isotope geochemistry to test potential proxies for calcium-to-alkalinity ratios (Ca:ALK). Across diverse carbonate facies from Pleistocene closed-basin lakes in Owens Valley, CA, we observed less δ44/40Ca variation than theoretically predicted (>0.75‰) for the very low Ca:ALK in these systems. Carbonate clumped isotope disequilibria implied rapid carbonate growth—kinetic isotope effects, combined with the diverse carbonate minerals present, complicated the interpretation of δ44/40Ca as a paleoalkalinity proxy. In contrast, we observed that the high phosphate concentrations are recorded by shoreline and lake bottom carbonates formed in 11 Pleistocene lakes at orders of magnitude greater concentrations than in marine carbonates. Because the maximum phosphate content of water depends on Ca:ALK, we propose that carbonate P/Ca can inform phosphate levels and thereby Ca:ALK of aqueous environments in the carbonate record.
AB - Understanding mechanisms, rates, and drivers of past carbonate formation provides insight into the chemical evolution of Earth's oceans and atmosphere. We paired geological observations with elemental and isotope geochemistry to test potential proxies for calcium-to-alkalinity ratios (Ca:ALK). Across diverse carbonate facies from Pleistocene closed-basin lakes in Owens Valley, CA, we observed less δ44/40Ca variation than theoretically predicted (>0.75‰) for the very low Ca:ALK in these systems. Carbonate clumped isotope disequilibria implied rapid carbonate growth—kinetic isotope effects, combined with the diverse carbonate minerals present, complicated the interpretation of δ44/40Ca as a paleoalkalinity proxy. In contrast, we observed that the high phosphate concentrations are recorded by shoreline and lake bottom carbonates formed in 11 Pleistocene lakes at orders of magnitude greater concentrations than in marine carbonates. Because the maximum phosphate content of water depends on Ca:ALK, we propose that carbonate P/Ca can inform phosphate levels and thereby Ca:ALK of aqueous environments in the carbonate record.
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U2 - 10.1029/2020GL088804
DO - 10.1029/2020GL088804
M3 - Article
AN - SCOPUS:85095932581
SN - 0094-8276
VL - 47
JO - Geophysical Research Letters
JF - Geophysical Research Letters
IS - 21
M1 - e2020GL088804
ER -