Search USGS⌕ Search

Geology topics

R.S. Parkhurst

Publications and source records attributed to R.S. Parkhurst.

6 recordsLinked to original sources

Characterization of lake water and ground water movement in the littoral zone of Williams Lake, a closed-basin lake in North central Minnesota

Williams Lake, Minnesota is a closed‐basin lake that is a flow‐through system with respect to ground water. Ground‐water input represents half of the annual water input and most of the chemical input to the lake. Chemical budgets indicate that the lake is a sink for calcium, yet surficial sediments contain little calcium carbonate. Sediment pore‐water samplers (peepers) were used to characterize solute fluxes at the lake‐water–ground‐water interface in the littoral zone and resolve the apparent disparity between the chemical budget and sediment data. Pore‐water depth profiles of the stable isotopes δ 18 O and δ 2 H were non‐linear where ground water seeped into the lake, with a sharp transition from lake‐water values to ground‐water values in the top 10 cm of sediment. These data indicate that advective inflow to the lake is the primary mechanism for solute flux from ground water. Linear interstitial velocities determined from δ 2 H profiles (316 to 528 cm/yr) were consistent with velocities determined independently from water budget data and sediment porosity (366 cm/yr). Stable isotope profiles were generally linear where water flowed out of the lake into ground water. However, calcium profiles were not linear in the same area and varied in response to input of calcium carbonate from the littoral zone and subsequent dissolution. The comparison of pore‐water calcium profiles to pore‐water stable isotope profiles indicate calcium is not conservative. Based on the previous understanding that 40–50 % of the calcium in Williams Lake is retained, the pore‐water profiles indicate aquatic plants in the littoral zone are recycling the retained portion of calcium. The difference between the pore‐water depth profiles of calcium and δ 18 O and δ 2 H demonstrate the importance of using stable isotopes to evaluate flow direction and source through the lake‐water–ground‐water interface and evaluate mechanisms controlling the chemical balance of lakes.

Minnesota↗

Evaporation from a small prairie wetland in the Cottonwood Lake area, North Dakota - An energy-budget study

Evaporation from Wetland P1 in the Cottonwood Lake area of North Dakota, USA was determined by the energy-budget method for 1982–85 and 1987. Evaporation rates were as high as 0.672 cm day −1 . Incoming solar radiation, incoming atmospheric radiation, and long-wave radiation emitted from the water body are the largest energy fluxes to and from the wetland. Because of the small heat storage of the water body, evaporation rates closely track solar radiation on short time scales. The effect of advected energy related to precipitation is small because the water quickly heats up by solar radiation following precipitation. Advected energy related to ground water is minimal because ground-water fluxes are small and ground-water temperature is only about 7 °C. Energy flux related to sediment heating and thermal storage in the sediments, which might be expected to be large because the water is clear and shallow, affects evaporation rates by less than 5 percent.

North Dakota↗

Selected chemical analyses of water from formations of Mesozoic and Paleozoic age in parts of Oklahoma, northern Texas, and Union County, New Mexico

Hydrochemical data were compiled into a data base as part of the Central Midwest Regional Aquifer System Analysis project. The data consist of chemical analyses of water samples collected from wells that are completed in formations of Mesozoic and Paleozoic age. The data base includes data from the National Water Data Storage and Retrieval System, the Petroleum Data System, the National Uranium Resource Evaluation, and selected publications. Chemical analyses were selected for inclusion within the hydrochemical data base if the total concentration of the cations differed from the total 10 percent or less of the total concentration of all ions. Those analyses which lacked the necessary data for an ionic balance were included if the ratios of dissolved-solids concentration to specific conductance were between 0.55 and 0.75. The tabulated chemical analyses, grouped by county, and a statistical summary of the analyses, listed by geologic unit, are presented.

Water-Resources Investigations Report↗