2007 GSA Denver Annual Meeting (28–31 October 2007)

Paper No. 1
Presentation Time: 8:00 AM

SOLUTE AND BACTERIAL TRANSPORT TO A KARST SPRING, INNER BLUEGRASS REGION, KENTUCKY


WARD, James W.1, FRYAR, Alan E.1, BRION, Gail M.2, COYNE, Mark3 and MACKO, Stephen A.4, (1)Earth & Environmental Sciences, University of Kentucky, 101 Slone Building, Lexington, KY 40506-0053, (2)Civil Engineering, Univ of Kentucky, 367 Raymond Building, Lexington, KY 40506-0281, (3)Plant and Soil Sciences, University of Kentucky, N-122 Agricultural Science Bldg, Lexington, KY 40546-0091, (4)Department of Environmental Sciences, University of Virginia, 291 McCormick Road, P.O. Box 400123, Charlottesville, VA 22904-4123, jameswadeward@gmail.com

Although techniques for conducting solute tracer tests in karst watersheds are well established, tracing the movement of bacterial pathogens is more challenging. From June 2006 to April 2007, we conducted three tracer tests under various flow conditions in a karst conduit system in Woodford County, Kentucky. Blue Hole Spring drains the city of Versailles (~ 8,000 population) and outlying farmland. Tracers were injected as slugs into a swallet ~ 500 m upgradient of the spring. Tracers consisted of solutes (rhodamine WT (RWT) fluorescent dye and bromide (Br-)), particles (1-µm fluorescent latex microspheres) and microorganisms (wild E. coli originally isolated from the spring and enriched in 15N).

The first trace occurred on June 2, 2006, under low-flow conditions and consisted of only solutes. Discharge averaged ~ 0.079 m3/s. RWT and Br- arrived at the spring ~ 6.16 hours and ~ 6.5 hours post-injection, respectively. The second trace occurred on July 11, 2006, under storm-flow conditions and consisted of solutes and particles. Discharge averaged 0.165 m3/s (maximum 0.262 m3/s) for this trace. Breakthrough began ~ 2.33 hours post-injection for the solutes and ~ 2.5 hours for the microspheres. Solute concentrations at the spring peaked ~ 2.67 hours after injection. Microspheres were detected at the spring until 164 hours after injection. The third trace transpired on April 1, 2007, during storm flow, and consisted of solutes, particles and mass growths of 15N-enriched E. coli. Discharge averaged 0.100 m3/s, with a maximum of 0.357 m3/s. Breakthrough began ~ 0.75 hours post-injection for the solutes and ~ 1.08 hours post- injection for the microspheres. For all three tests, breakthrough curves for the solutes were smooth, yet the microsphere breakthrough curves were jagged. Subsequent storm-flow pulses resuspended microspheres that had settled out following initial injections. Enriched E. coli breakthrough results are pending.