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C. P. Carney

Publications and source records attributed to C. P. Carney.

2 recordsLinked to original sources

Use of geochemical, isotopic, and age tracer data to develop models of groundwater flow for the purpose of water management, northern High Plains aquifer, USA

A prolonged drought in the High Plains of Nebraska prompted the use of groundwater for cooling at the largest coal-fired power plant in the State. Prior to the drought, groundwater was used primarily for irrigation and the power plant relied exclusively on surface water stored in a nearby reservoir for cooling. Seepage from the reservoir system during the past ∼75 a has resulted in the buildup of a large mound of water in the underlying unconfined aquifer. A well field was installed during the drought for the purpose of tapping the groundwater mound as a supplemental source of water for cooling. Concentrations of dissolved Cl − and SO 4 2 - "> SO 4 2- indicate 65–100% of shallow groundwater and 0–100% of deep groundwater (saturated thickness ∼115 m) in the immediate vicinity of the reservoir was from seepage out of the reservoir system. Hydrogen and O isotopic data indicate most surface-water seepage occurred in the late spring and early summer when reservoir stage was at its highest level. Tritium/ 3 He apparent groundwater ages imply horizontal flow velocities from the reservoir were on the order of 60–600 m/a. These diverse data provided information regarding the spatial distribution, timing, and rate of seepage from the reservoir that could not have been obtained from the available geologic, hydraulic head, and conductivity data. In particular, mixing fractions of surface water and regional groundwater in the aquifer could not have been determined using hydraulic information. Mixing fractions were of special interest in this study because of the management objective to maximize the capture of surface-water seepage in the cooling water wells. Groundwater-flow models developed as well-field management tools were calibrated using inverse modeling techniques and observations of groundwater age, surface-water flow, reservoir stage, and groundwater levels. The age data only accounted for 6 of the 2574 field observations used to calibrate the groundwater-flow models, yet they were among the most influential for refining estimates of hydraulic conductivity, recharge, and seepage from the reservoir. Results from this study demonstrate the benefits of using geochemical, isotopic, and age tracer data to develop conceptual and numerical models of groundwater flow for the purpose of water management.

Nebraska

Vertical gradients in water chemistry and age in the Northern High Plains Aquifer, Nebraska, 2003

The northern High Plains aquifer is the primary source of water used for domestic, industrial, and irrigation purposes in parts of Colorado, Kansas, Nebraska, South Dakota, and Wyoming. Despite the aquifer’s importance to the regional economy, fundamental ground-water characteristics, such as vertical gradients in water chemistry and age, remain poorly defined. As part of the U.S. Geological Survey’s National Water-Quality Assessment Program, water samples from nested, short-screen monitoring wells installed in the northern High Plains aquifer were analyzed for major ions, nutrients, trace elements, dissolved organic carbon, pesticides, stable and radioactive isotopes, dissolved gases, and other parameters to evaluate vertical gradients in water chemistry and age in the aquifer. Chemical data and tritium and radiocarbon ages show that water in the aquifer was chemically and temporally stratified in the study area, with a relatively thin zone of recently recharged water (less than 50 years) near the water table overlying a thicker zone of older water (1,800 to 15,600 radiocarbon years). In areas where irrigated agriculture was an important land use, the recently recharged ground water was characterized by elevated concentrations of major ions and nitrate and the detection of pesticide compounds. Below the zone of agricultural influence, major-ion concentrations exhibited small increases with depth and distance along flow paths because of rock/water interactions. The concentration increases were accounted for primarily by dissolved calcium, sodium, bicarbonate, sulfate, and silica. In general, the chemistry of ground water throughout the aquifer was of high quality. None of the approximately 90 chemical constituents analyzed in each sample exceeded primary drinking-water standards. Mass-balance models indicate that changes in groundwater chemistry along flow paths in the aquifer can be accounted for by small amounts of feldspar and calcite dissolution; goethite and clay-mineral precipitation; organic-carbon and pyrite oxidation; oxygen reduction and denitrification; and cation exchange. Mixing with surface water affected the chemistry of ground water in alluvial sediments of the Platte River Valley. Radiocarbon ages in the aquifer, adjusted for carbon mass transfers, ranged from 1,800 to 15,600 14C years before present. These results have important implications with respect to development of ground-water resources in the Sand Hills. Most of the water in the aquifer predates modern anthropogenic activity so excessive removal of water by pumping is not likely to be replenished by natural recharge in a meaningful timeframe. Vertical gradients in ground-water age were used to estimate long-term average recharge rates in the aquifer. In most areas, the recharge rates ranged from 0.02 to 0.05 foot per year. The recharge rate was 0.2 foot per year in one part of the aquifer characterized by large downward hydraulic gradients. Nitrite plus nitrate concentrations at the water table were 0.13 to 3.13 milligrams per liter as nitrogen, and concentrations substantially decreased with depth in the aquifer. Dissolved-gas and nitrogen-isotope data indicate that denitrification in the aquifer removed 0 to 97 percent (average = 50 percent) of the nitrate originally present in recharge. The average amount of nitrate removed by denitrification in the aquifer north of the Platte River (Sand Hills) was substantially greater than the amount removed south of the river (66 as opposed to 0 percent), and the extent of nitrate removal appears to be related to the presence of thick deposits of sediment on top of the Ogallala Group in the Sand Hills that contained electron donors, such as organic carbon and pyrite, to support denitrification. Apparent rates of dissolved-oxygen reduction and denitrification were estimated on the basis of decreases in dissolved-oxygen concentrations and increases in concentrations of excess nitrogen gas and ground-water ages along flow paths from the water table to deeper wells. Median rates of dissolved-oxygen reduction and denitrification south of the Platte River were at least 10 times smaller than the median rates north of the river in the Sand Hills. The relatively large denitrification rates in the Sand Hills indicate that the aquifer in that area may have a greater capacity to attenuate nitrate contamination than the aquifer south of the river, depending on rates of ground-water movement in the two areas. Small denitrification rates south of the river indicate that nitrate contamination in that part of the aquifer would likely persist for a longer period of time.

Nebraska