2003 Seattle Annual Meeting (November 2–5, 2003)

Paper No. 11
Presentation Time: 11:10 AM

234U/238U DISEQUILLIBRIUM AS AN ENVIRONMENTAL TRACER OF GROUND-WATER DISCHARGE TO SPRINGS IN THE UPPER VERDE RIVER HEADWATERS REGION, NORTH CENTRAL ARIZONA


WIRT, Laurie, U.S. Geol Survey, PO Box 25046, MS 973, Denver Federal Center, Denver, CO 80225 and KETTERER, Michael E., Department of Chemistry, Northern Arizona Univ, Box 5698, Flagstaff, AZ 86011-5698, lwirt@usgs.gov

Discharge springs from two basin-fill aquifers and the regional Paleozoic limestone aquifer at the headwaters of the Verde River each have distinctive 234U/238U activity ratios (ARs). The headwaters region drains the transition zone between the Colorado Plateau and the Basin and Range physiographic provinces in north-central Arizona. ARs and U concentrations can be used to evaluate water sources and their mixing. The marine carbonate (Paleozoic aquifer) had the lowest uranium concentrations (0.6 to 0.8 µg/L) and highest ARs (4.0 to 9.2), suggestive of slow leaching of U over long time periods and preferential dissolution of 234U by decay-related alpha recoil. In contrast, the basin-fill aquifers are characterized by relatively constant AR of 3.0+0.3 and variable U concentrations. Each basin-fill aquifer represents the integration of many inputs from recharge area springs that drain a variety of upland rock types (Precambrian granite and gneiss, carbonate, sedimentary, and volcanic rocks), with igneous and metamorphic rocks containing the most uranium. U concentrations ranged from about 1.0 µg/L in wells near large ephemeral streams, to 4.2 µg/L near the outlet of the two basin-fill aquifers, where ground water is in contact with younger igneous rocks (30-Ma volcanic latite and 5-Ma basalts) with the dominant AR of 3.0+0.3. ARs of 15 springs in the first 2 km of the Verde River vary between 2.5 and 3.7, with U concentrations from 0.8 to 5.0 µg/L—indicating numerous distinct seeps, each with a unique flow path. The final AR and U concentration of the river were 3.7 and 3.1 µg/L, representing a flow-weighted composite of multiple seeps. Rapid, high precision measurements of uranium-series isotopes by quadrupole inductively coupled plasma mass spectrometry can greatly expand applications of uranium-series isotopes as environmental tracers.