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At least 649 records · Page 36Linked to original sources
USGS1994

Effects of ground-water chemistry and flow on quality of drainflow in the western San Joaquin Valley, California

Chemical and geohydrologic data were used to assess the effects of regional ground-water flow on the quality of on-farm drainflows in a part of the western San Joaquin Valley, California. Shallow ground water beneath farm fields has been enriched in stable isotopes and salts by partial evaporation from the shallow water table and is being displaced by irrigation, drainage, and regional ground-water flow. Ground-water flow is primarily downward in the study area but can flow upward in some down- slope areas. Transitional areas exist between the downward and upward flow zones, where ground water can move substantial horizontal distances (0.3 to 3.6 kilometers) and can require 10 to 90 years to reach the downslope drainage systems. Simulation of ground-water flow to drainage systems indicates that regional ground water contributes to about 11 percent of annual drainflow. Selenium concentrations in ground water and drainwater are affected by geologic source materials, partial evaporation from a shallow water table, drainage-system, and regional ground-water flow. Temporal variability in drainflow quality is affected in part by the distribution of chemical constituents in ground water and the flow paths to the drainage systems. The mass flux of selenium in drainflows, or load, generally is proportional to flow, and reductions in drainflow quantity should reduce selenium loads over the short-term. Uncertain changes in the distribution of ground-water quality make future changes in drainflow quality difficult to quantify.

Open-File Report↗
USGS1997

Precipitation-chemistry data at selected sites in northwestern Colorado, 1980-94

The chemical content of precipitation was monitored during the period 1980-94 at three sites at altitudes above 2,400 meters near the Piceance Basin in northwestern Colorado. Daily precipitation volumes, specific conductance, pH (in this report pH is expressed as hydrogen-ion concentration), concentrations of major cations and anions, calculated charge balance between cations and anions, and summary statistics of chemical concentrations are tabulated. Sampling sites are plotted on a map of the area. Seasonal variabilities of major cation and anion concentrations are presented graphically.

Open-File Report↗
USGS1998

Water-chemistry and on-site sulfur-speciation data for selected springs in Yellowstone National Park, Wyoming, 1994-1995

Forty-two water analyses are reported for samples collected at 8 hot springs and their overflow drainages, two geysers, and two ambient-temperature acid streams in Yellowstone National Park during 1994-95. These water samples were collected and analyzed as part of the initial research investigations on sulfur redox speciation in the hot springs of Yellowstone and to document chemical changes in overflows that affect major ions, redox species, and trace elements. The sulfur redox speciation research is a collaboration between the State University of New York (SUNY) at Stony Brook and the U.S. Geological Survey (USGS). Four hot springs, Ojo Caliente, Azure, Frying Pan, and Angel Terrace, were studied in detail. Analyses were performed adjacent to the sampling site or in an on-site mobile lab truck constructed by the USGS, or later in a USGS laboratory. Water temperature, specific conductance, pH, Eh, D.O., and dissolved H2S were determined adjacent to the sample source at the time of sampling. Alkalinity and F- were determined on-site on the day of sample collection. Thiosulfate and polythionates were determined as soon as possible (minutes to hours later) by ion chromatography (IC). Other major anions (Cl-, SO4 2-, Br-) also were determined on-site by IC within two days of sample collection. Ammonium, Fe(II), and Fe(total) were determined on-site by ultraviolet/visible spectrophotometry within two days of sample collection. Later in the USGS laboratory, densities were determined. Concentrations of Ca, Mg, Li, Na, and K were determined by flame atomic absorption and emission (Na, K) spectrometry. Concentrations of Al, As, B, Ba, Be, Ca, Cd, Co, Cr, Cu, Fe(total), K, Mg, Mn, Na, Ni, Pb, Si, Sr, V, and Zn were determined by inductively-coupled plasma optical emission spectrometry. Trace concentrations of Al and Mg were determined by Zeeman-corrected graphite furnace atomic absorption spectrometry. Three important conclusions from the sampling and analyses are: (1) variability in H2S concentrations can be caused as much by sampling and preservation artifacts as by actual variations in water composition over time, (2) historical determinations of S2O3 2- were subject to overestimation, most likely because of inadequate preservation leading to H2S oxidation, and (3) S2O3 2- is a common constituent of hot spring waters.

Wyoming↗
USGS2001

Stratigraphic section and selected semiquantitative chemistry, Meade Peak phosphatic shale member of Permian Phosphoria Formation, central part of Rasmussen Ridge, Caribou County, Idaho

The U.S. Geological Survey (USGS) has studied the Permian Phosphoria Formation in southeastern Idaho and the entire Western U.S. Phosphate Field throughout much of the twentieth century. In response to a request by the U.S. Bureau of Land Management, a new series of resource, geological, and geoenvironmental studies was undertaken by the USGS in 1998. To accomplish these studies, the USGS has formed cooperative research relationships with two Federal agencies, the Bureau of Land Management and the U.S. Forest Service, tasked with land management and resource conservation on public lands; and with five private companies currently leasing or developing phosphate resources in southeastern Idaho. The companies are Agrium U.S. Inc. (Rasmussen Ridge mine) , Astaris LLC (Dry Valley mine), Rhodia Inc. (Wooley Valley mine, inactive), J.R. Simplot Company (Smoky Canyon mine), and Monsanto Co. (Enoch Valley mine). Some of the mineralogical research associated with this project is supported through a cooperative agreement with the Department of Geology and Geological Enginee ring, University of Idaho. Present studies consist of integrated, multidisciplinary research directed toward (1) resource and reserve estimations of phosphate in selected 7.5-minute quadrangles; (2) elemental residence, mineralogical and petrochemical characteristics; (3) mobilization and reaction pathways, transport, and fate of potentially toxic elements associated with the occurrence, development, and societal use of phosphate; (4) geophysical signatures; and (5) improving the understanding of deposit origin. Because raw data acquired during the project will require time to interpret, the data are released in open-file reports for prompt availability to other workers. Open-file reports associated with this series of studies are submitted to each of the Federal and industry cooperators for comment; however, the USGS is solely responsible for the data contained in the reports.

Idaho↗