Abstract
Summary The tritium concentration in the surface hydrosphere throughout California was characterized to examine the reasons for spatial variability and to enhance the applicability of tritium in hydrological investigations. Eighteen precipitation samples were analyzed and 148 samples were collected from surface waters across California in the Summer and Fall of 2013, with repeat samples from some locations collected in Winter and Spring of 2014 to examine seasonal variation. The concentration of tritium in present day precipitation varied from 4.0 pCi/L near the California coast to 17.8 pCi/L in the Sierra Nevada Mountains. Concentrations in precipitation increase in spring due to the ‘Spring Leak’ phenomenon. The average coastal concentration (6.3 ± 1.2 pCi/L) in precipitation matches estimated pre-nuclear levels. Surface water samples show a trend of increasing tritium with inland distance. Superimposed on that trend, elevated tritium concentrations are found in the San Francisco Bay area compared to other coastal areas, resulting from municipal water imported from inland mountain sources and local anthropogenic sources. Tritium concentrations in most surface waters decreased between Summer/Fall 2013 and Winter/Spring 2014 likely due to an increased groundwater signal as a result of drought conditions in 2014. A relationship between tritium and electrical conductivity in surface water was found to be indicative of water provenance and anthropogenic influences such as agricultural runoff. Despite low initial concentrations in precipitation, tritium continues to be a valuable tracer in a post nuclear bomb pulse world.
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