Sources and fractionation processes influencing the isotopic distribution of H, O and C in the Long Valley hydrothermal system, California, U.S.A.
The isotopic ratios of H, O and C in water within the Long Valley caldera, California reflect input from sources external to the hydrothermal reservoir. A decrease in δD in precipitation of 0.5‰ km −1 , from west to east across Long Valley, is caused by the introduction of less fractionated marine moisture through a low elevation embayment in the Sierra Nevada Mountain Range. Relative to seasonal fluctuations in precipitation (−158 to −35‰.), δD ranges in hot and cold surface and groundwaters are much less variable (−135 to −105‰.). Only winter and spring moisture, reflecting higher precipitation rates with lighter isotopic signatures, recharge the hydrological system. The hydrothermal fluids are mixtures of isotopically heavy recharge (δD = − 115‰, δ 18 O = − 15‰) derived from the Mammoth embayment, and isotopically lighter cold water (δD = −135‰, δ 18 O = −18‰). This cold water is not representative of current local recharge. The δ 13 C values for dissolved carbon in hot water are significantly heavier (− 7 to − 3‰) than in cold water (−18 to −10‰) denoting a separate hydrothermal origin. These δ 13 C values overlie the range generally attributed to magmatic degassing of CO 2 . However, δ 13 C values of metamorphosed Paleozoic basement carbonates surrounding Long Valley fall in a similar range, indicating that hydrothermal decarbonization reactions are a probable source of CO 2 . The δ 13 C and δ 18 O values of secondary travertime and vein calcite indicate respective fractionation with CO 2 and H 2 O at temperatures approximating current hydrothermal conditions.