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Research about central High Plains aquifer

Source-linked reports with geographic coverage including central High Plains aquifer.

2 recordsLinked to original sources

Ground-water quality in the central High Plains aquifer, Colorado, Kansas, New Mexico, Oklahoma, and Texas, 1999

A network of 74 randomly distributed domestic water-supply wells completed in the central High Plains aquifer was sampled and analyzed from April to August 1999 as part of the High Plains Regional Ground-Water Study conducted by the U. S. Geological Survey National Water-Quality Assessment Program to provide a broad-scale assessment of the ground-water-quality in this part of the High Plains aquifer. Water properties were relatively consistent across the aquifer, with water being alkaline and well oxidized. Water was mostly of the calcium and magnesium-bicarbonate type and very hard. Sulfate concentrations in water from three wells and chloride concentration in water from one well exceeded Secondary Maximum Contaminant Levels. Fluoride concentration was equal to the Maximum Contaminant Level in one sample. Nitrate concentrations was relatively small in most samples, with the median concentration of 2.3 milligrams per liter. Dissolved organic carbon concentration was relatively low, with a median concentration of 0.5 milligram per liter. The Maximum Contaminant Level set by the U.S. Environmental Protection Agency for nitrate as nitrogen of 10 milligrams per liter was exceeded by water samples from three wells. Most samples contained detectable concentrations of the trace elements aluminum, arsenic, barium, chromium, molybdenum, selenium, zinc, and uranium. Only a few samples had trace element concentrations exceeding Maximum Contaminant Levels. Fifty-five of the samples had radon concentrations exceeding the proposed Maximum Contaminant Level of 300 picocuries per liter. The greatest radon concentrations were detected where the Ogallala Formation overlies sandstones, shales and limestones of Triassic, Jurassic, or Cretaceous age. Volatile organic compounds were detected in 9 of 74 samples. Toluene was detected in eight of those nine samples. All volatile organic compound concentrations were substantially less than Maximum Contaminant Levels. Detections of toluene may have been artifacts of the sampling and analytical processes. Pesticides were detected in 18 of the 74 water samples. None of the pesticide concentrations exceeded Maximum Contaminant Levels. The most frequently detected pesticides were atrazine and its metabolite deethylatrazine, which were detected in water from 15 and 17 wells, respectively. Most of the samples with a detectable pesticide had at least two detectable pesticides. Six of the samples had more than two detectable pesticides. Tritium concentrations was greater than 0.5 tritium unit in 10 of 51 samples, indicating recent recharge to the aquifer. Twenty-one of the samples that had nitrate concentrations greater than 4.0 milligrams per liter were assumed to have components of recent recharge. Detection of volatile organic compounds was not associated with those indicators of recent recharge, with most of volatile organic compounds being detected in water from wells with small tritium and nitrate concentrations. Detection of pesticides was associated with greater tritium or nitrate concentrations, with 16 of the 18 wells producing water with pesticides also having tritium or nitrate concentrations indicating recent recharge.

Colorado, Kansas, New Mexico, Oklahoma, Texas↗

Vertical gradients in water chemistry in the central High Plains aquifer, southwestern Kansas and Oklahoma panhandle, 1999

The central High Plains aquifer is the primary source of water for domestic, industrial, and irrigation uses in parts of Colorado, Kansas, New Mexico, Oklahoma, and Texas. Water-level declines of more than 100 feet in some areas of the aquifer have increased the demand for water deeper in the aquifer. The maximum saturated thickness of the aquifer ranged from 500 to 600 feet in 1999. As the demand for deeper water increases, it becomes increasingly important for resource managers to understand how the quality of water in the aquifer changes with depth. In 1998­99, 18 monitoring wells at nine sites in southwestern Kansas and the Oklahoma Panhandle were completed at various depths in the central High Plains aquifer, and one monitoring well was completed in sediments of Permian age underlying the aquifer. Water samples were collected once from each well in 1999 to measure vertical gradients in water chemistry in the aquifer. Tritium concentrations measured in ground water indicate that water samples collected in the upper 30 feet of the aquifer were generally recharged within the last 50 years, whereas all of the water samples collected at depths more than 30 feet below the water table were recharged more than 50 years ago. Dissolved oxygen was present throughout the aquifer, with concentrations ranging from 1.7 to 8.4 mg/L. Water in the central High Plains aquifer was predominantly a calcium-bicarbonate type that exhibited little variability in concentrations of dissolved solids with depth (290 to 642 mg/L). Exceptions occurred in some areas where there had been upward movement of mineralized water from underlying sediments of Permian age and areas where there had been downward movement of mineralized Arkansas River water to the aquifer. Calcium-sulfate and sodium-chloride waters dominated and concentrations of dissolved solids were elevated (862 to 4,030 mg/L) near the base of the aquifer in the areas of upward leakage. Dissolution of gypsum or anhydrite and halite in sediments of Permian age by ground water was the likely source of calcium, sulfate, sodium, and chloride in those waters. Calcium-sodium-sulfate waters dominated, and concentrations of dissolved solids were as large as 4,916 mg/L near the water table in the area of downward leakage. Dissolution of minerals in sedimentary deposits of marine origin in upstream areas of the Arkansas River drainage were the likely sources of calcium, sodium, and sulfate in those waters. Nitrate was detected throughout the aquifer and the background concentration was estimated to be 2.45 mg/L as N. The largest nitrate concentrations (8.28, 22, and 54.4 mg/L as N) occurred in recently recharged water collected adjacent to irrigated fields. Three pesticides (atrazine, metolachlor, simazine) and five pesticide degradation products (alachlor ethanesulfonic acid, alachlor oxanilic acid, deethylatrazine, metolachlor ethanesulfonic acid, metolachlor oxanilic acid) were detected in recently recharged water from six water-table wells. Five of the six wells were adjacent to irrigated fields. These data indicate that concentrations of nitrate and pesticides increased over time in some areas of the aquifer as a result of agricultural activities. Results from this study indicate that vertical gradients in water chemistry existed in the central High Plains aquifer. The chemical gradients resulted from chemical inputs to the aquifer from underlying sediments of Permian age, from the Arkansas River, and from agricultural activities. In areas where those chemical inputs occurred, water quality in the aquifer was impaired and may not have been suitable for some intended uses.

Kansas, Oklahoma↗