Search USGS⌕ Search

SEARCH · Search USGS

Results for “Chemical Physics”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 145 records · Page 8Linked to original sources
USGS2013

The quality of our Nation’s waters--Ecological health in the Nation's streams, 1993-2005

This report summarizes a national assessment of the ecological health of streams done by the U.S. Geological Survey's (USGS) National Water-Quality Assessment Program (NAWQA). Healthy functioning stream ecosystems provide society with many benefits, including water purification, flood control, nutrient recycling, waste decomposition, fisheries, and aesthetics. The value to society of many of these benefits is substantial; for example, sportfishing in the United States generates an estimated annual economic output of $125 billion, including more than 1 million jobs (National Research Council, 2005; American Sportfishing Association, 2008). Continued monitoring and assessment of the Nation’s streams is needed to support informed decisions that will safeguard this important natural and economic resource. The quality of streams and rivers is often assessed with measures of the chemical or physical properties of water. However, a more comprehensive perspective is obtained if resident biological communities are also assessed. Guidelines to protect human health and aquatic life have been established for specific physical and chemical properties of water and have become useful yardsticks with which to assess water quality. Biological communities provide additional crucial information because they live within streams for weeks to years and therefore integrate through time the effects of changes to their chemical or physical environment. In addition, biological communities are a direct measure of stream health—an indicator of the ability of a stream to support aquatic life. Thus, the condition of biological communities, integrated with key physical and chemical properties, provides a comprehensive assessment of stream health.

conterminous United States↗
USGS2009

Rocky Mountain Snowpack Physical and Chemical Data for Selected Sites, 1993-2008

The Rocky Mountain Snowpack program established a network of snowpack-sampling sites in the Rocky Mountain region from New Mexico to Montana to monitor the chemical content of snow to help in the understanding of the effects of atmospheric deposition to this region. The U.S. Geological Survey, in cooperation with the National Park Service, the USDA Forest Service, Teton County in Wyoming, Rio Blanco County in Colorado, Pitkin County in Colorado, and others, collected and analyzed snowpack samples annually for 48 or more sites in the Rocky Mountain region during 1993-2008. Forty-eight of the 162 snow-sampling sites have been sampled annually since 1993. Data include acid-neutralization capacity, specific conductance, pH, hydrogen ion concentrations, dissolved concentrations of major constituents (calcium, magnesium, sodium, potassium, ammonium, chloride, sulfate, and nitrate), dissolved organic carbon concentrations, snow/ water equivalent, snow depth, stable sulfur isotope ratios, total mercury concentrations (beginning in 2001), and ionic charge balance. Quality-assurance data for field and laboratory blanks and field replicates for individual years (1993-2008) also are included.

Data Series↗
USGS2010

Rocky Mountain snowpack physical and chemical data for selected sites, 2009

The Rocky Mountain Snowpack program established a network of snowpack-sampling sites in the Rocky Mountain region from New Mexico to Montana to monitor the chemical content of snow and to understand the effects of regional atmospheric deposition. The U.S. Geological Survey, in cooperation with the National Park Service; the U.S. Department of Agriculture Forest Service; the Colorado Department of Public Health and Environment; Teton County, Wyoming; and others, collected and analyzed snowpack samples annually for 48 or more sites in the Rocky Mountain region during 1993-2009. Sixty-three snowpack-sampling sites were sampled once each in 2009 and data are presented in this report. Data include acid-neutralization capacity, specific conductance, pH, hydrogen ion concentrations, dissolved concentrations of major constituents (calcium, magnesium, sodium, potassium, ammonium, chloride, sulfate, and nitrate), dissolved organic carbon concentrations, snow-water equivalent, snow depth, total mercury concentrations, and ionic charge balance. Quality-assurance data for field and laboratory blanks and field replicates for 2009 also are included.

Data Series↗
USGS2011

Rocky Mountain snowpack physical and chemical data for selected sites, 2010

The Rocky Mountain Snowpack program established a network of snowpack-sampling sites in the Rocky Mountain region, from New Mexico to Montana, to monitor the chemical content of snow and to understand the effects of regional atmospheric deposition on freshwater systems. Scientists with the U.S. Geological Survey, in cooperation with the National Park Service; the U.S. Department of Agriculture Forest Service; the Colorado Department of Public Health and Environment; Teton County, Wyoming; and others, annually collected and analyzed snow-pack samples at 48 or more sites in the Rocky Mountain region during 1993-2010. Sixty-three snowpack-sampling sites were each sampled once in 2010, and those data are presented in this report. Data include acid-neutralization capacity, specific conductance, pH, hydrogen ion concentrations, dissolved concentrations of major constituents (calcium, magnesium, sodium, potassium, ammonium, chloride, sulfate, and nitrate), dissolved organic carbon concentrations, snow-water equivalent, snow depth, total mercury concentrations, and ionic charge balance. Quality-assurance data for field and laboratory blanks and field replicates for 2010 also are included.

Rocky Mountains↗
USGS2000

Abrupt physical and chemical changes during 1992-1999, Anderson Springs, SE Geyser Geothermal Field, California

The Anderson Springs area is located about 90 miles (145 kilometers) north of San Francisco, California, in the southwestern part of Lake County. The area was first developed in the late 1800s as a health resort, which was active until the 1930s. Patrons drank a variety of cool to hot mineral waters from improved springs, swam in various baths and pools, and hiked in the rugged hills flanking Anderson Creek and its tributaries. In the bluffs to the south of the resort were four small mercury mines of the eastern Mayacmas quicksilver district. About 1,260 flasks of mercury were produced from these mines between 1909 and 1943. By the early 1970s, the higher ridges south and west of Anderson Springs became part of the southeast sector of the greater Geysers geothermal field. Today, several electric power plants are built on these ridges, producing energy from a vapor-dominated 240 °C reservoir. Only the main hot spring at Anderson Springs has maintained a recognizable identity since the 1930s. The hot spring is actually a cluster of seeps and springs that issue from a small fault in a ravine southwest of Anderson Creek. Published and unpublished records show that the maximum temperature (Tm) of this cluster fell gradually from 63°C in 1889 to 48°C in 1992. However, Tm of the cluster climbed to 77°C in 1995 and neared boiling (98°C) in 1998. A new cluster of boiling vents and small fumaroles (Tm = 99.3°C) formed in 1998 about 30 m north of the old spring cluster. Several evergreen trees on steep slopes immediately above these vents apparently were killed by the new activity. Thermal waters at Anderson Hot Springs are mostly composed of near-surface ground waters with some added gases and condensed steam from The Geysers geothermal system. Compared to gas samples from Southeast Geysers wells, the hot spring gases are higher in CO 2 and lower in H 2 S and NH 3 . As the springs increased in temperature, however, the gas composition became more like the mean composition of steam discharges from the Southeast Geysers. The hot spring waters are low in ions of Cl, B, and Li, but relatively high in HCO 3 , SO 4 and NH 4 . The stable-isotope compositions (deuterium and oxygen-18) of these waters plot near the global meteoric water line. Geochemical data through time reveal apparent maxima in the concentrations of SO 4 , Fe, and Mn in 1991 to 1992, before the cluster became hotter. The black-to-gray deposits from the new spring cluster are rich in pyrite and contain anomalous metals. About one-half mile to the east of the hot springs, mineralized water discharges intermittently from an old adit of the Schwartz (Anderson) mine, and enters a tributary of Anderson Creek. This drainage increased substantially in July 1998, and a slurry of mine water and precipitates were transported down the tributary and into Anderson Creek. In December 1998, the adit water was 22°C, and had a chemical composition that was similar to spring waters that once discharged in the ravines surrounding the old Anderson Springs resort. The cause for the abrupt changes that have occurred in thermal features at Anderson Springs is still not resolved. One possibility is that these changes are a response to withdrawal of steam from The Geysers geothermal field over more than 20 years of production. Pressure declines in the geothermal reservoir may have caused a "drying out" of the overlying condensation zone. Induced boiling in this zone and upflow of deep steam to shallower depths would cause heating and vaporization of shallow ground waters. In addition, earthquakes occurring in the vicinity of Anderson Springs have increased significantly after nearby geothermal power plants began operation. These earthquakes may have enhanced surface discharge of thermal fluids along fractures and faults.

California↗
USGS2010

Biological, Physical, And Chemical Data From Gulf of Mexico Core PE0305-GC1

This paper presents benthic foraminiferal census data, and magnetic susceptibility, 210Pb , radiocarbon, and geochemical measurements from gravity core PE0305-GC1 (=GC1). Core GC1 was collected from the Louisiana continental shelf as part of an initiative to investigate the geographic and temporal extent of hypoxia, low-oxygen water, in the Gulf of Mexico. Hypoxia (<1.4 ml/l or <2 ppm oxygen concentration) in Gulf of Mexico waters can eventually lead to death of marine species. The development of hypoxia off the Mississippi delta has increased steadily since routine and systematic measurements were begun in 1985 and has been linked to the use of fertilizer in the Mississippi basin. Benthic foraminifers provide a proxy to track the development of hypoxia prior to 1985. Previous work determined that the relative occurrence of three low-oxygen-tolerant species is highest in the hypoxia zone. The cumulative percentage of these three species (% Pseudononion atlanticum + % Epistominella vitrea, + % Buliminella morgani = PEB index of hypoxia) was used to investigate fluctuation in paleohypoxia in four cores, including the upper 60 cm of GC1. In this report, we compile all available data from GC1 as the basis for further publications.

Open-File Report↗
USGS2010

Biological, Physical and Chemical Data From Gulf of Mexico Gravity and Box Core MRD05-04

This paper presents the benthic foraminiferal census data, magnetic susceptibility measurements, vanadium and organic geochemistry (carbon isotope, sterols, and total organic carbon) data from the MRD05-04 gravity and box cores. The MRD05-04 cores were obtained from the Louisiana continental shelf in an on-going initiative to examine the geographic and temporal extent of hypoxia, low-oxygen bottom-water content, and geochemical transport. The development of low-oxygen bottom water conditions in coastal waters is dependent upon a new source of bio-available nutrients introduced into a well-stratified water column. A number of studies have concluded that the development of the current seasonal hypoxia (dissolved oxygen < 2 mg L-1) in subsurface waters of the northern Gulf of Mexico is related to increased transport of nutrients (primarily nitrogen, but possibly also phosphorous) by the Mississippi River. However, the development of earlier episodes of seasonal low-oxygen subsurface water on the Louisiana shelf may be related to Mississippi River discharge.

Open-File Report↗
USGS2007

Physical and Chemical Data from Eolian Sediment Collected Along a Transect from the Mojave Desert to the Colorado Plateau

This report presents data and describes the methodology for magnetic, geochemical, and textural measurements of sediment and bedrock samples collected along a transect across the Southwestern United States (fig. 1). The results presented here support a study that examines compositional variations of mineral dust deposited during the past few centuries in isolated natural traps spanning a region from the Mojave Desert of southern California to the central Colorado Plateau (Goldstein and others, in press; fig. 1). In particular, the study addresses the spatial and temporal variations in dust composition in the context of landscape geochemistry over a large area of the southwestern United States.

Open-File Report↗
USGS2011

Physical and chemical characteristics including total and geochemical forms of phosphorus in sediment from the top 30 centimeters of cores collected in October 2006 at 26 sites in Upper Klamath Lake, Oregon

&mu;This study of phosphorus (P) cycling in eutrophic Upper Klamath Lake (UKL), Oregon, was conducted by the U.S. Geological Survey in cooperation with the U.S. Bureau of Reclamation. Lakebed sediments from the upper 30 centimeters (cm) of cores collected from 26 sites were characterized. Cores were sampled at 0.5, 1.5, 2.5, 3.5, 4.5, 10, 15, 20, 25, and 30 cm. Prior to freezing, water content and sediment pH were determined. After being freeze-dried, all samples were separated into greater than 63-micron (&mu;m) particle-size (coarse) and less than 63-&mu;m particle-size (fine) fractions. In the surface samples (0.5 to 4.5 cm below the sediment water interface), approximately three-fourths of the particles were larger than 63-&mu;m. The ratios of the coarse particle-size fraction (>63 &mu;m) and the fine particle-size fraction (<63 &mu;m) were approximately equal in samples at depths greater than 10 cm below the sediment water interface. Chemical analyses included both size fractions of freeze-dried samples. Chemical analyses included determination of total concentrations of aluminum (Al), calcium (Ca), carbon (C), iron (Fe), poorly crystalline Fe, nitrogen (N), P, and titanium (Ti). Total Fe concentrations were the largest in sediment from the northern portion of UKL, Howard Bay, and the southern portion of the lake. Concentrations of total Al, Ca, and Ti were largest in sediment from the northern, central, and southernmost portions of the lake and in sediment from Howard Bay. Concentrations of total C and N were largest in sediment from the embayments and in sediment from the northern arm and southern portion of the lake in the general region of Buck Island. Concentrations of total C were larger in the greater than 63-&mu;m particle-size fraction than in the less than 63-&mu;m particle-size fraction. Sediments were sequentially extracted to determine concentrations of inorganic forms of P, including loosely sorbed P, P associated with poorly crystalline Fe oxides, and P associated with mineral phases. The difference between the concentration of total P and sum of the concentrations of inorganic forms of P is referred to as residual P. Residual P was the largest fraction of P in all of the sediment samples. In UKL, the correlation between concentrations of total P and total Fe in sediment is poor (R2<0.1). The correlation between the concentrations of total P and P associated with poorly crystalline Fe oxides is good (R2=0.43) in surface sediment (0.5-4.5 cm below the sediment water interface) but poor (R2<0.1) in sediments at depths between 10 cm and 30 cm. Phosphorus associated with poorly crystalline Fe oxides is considered bioavailable because it is released when sediment conditions change from oxidizing to reducing, which causes dissolution of Fe oxides.

Oregon↗
USGS1977

Chemical analysis, physical property tests, and lithologic description of cores and cuttings of lignite and overburden rocks from an area near Watkins, Colorado

The data presented in this report represents analytical and testing information from cores drilled by the Geophysics Department, Colorado School of Mines, assisted by the U.S. Geological Survey. The drilling was done in conjunction with the establishment of a geophysical testing facility by the Colorado School of Mines. Location of the study area and drill holes is shown in Figure 1. A total of 15 holes were drilled and geophysically logged; holes 9-1 and 7-11 were cored, and attempts to core hole 3-1 were made, but the lignite was very incompetent due to weathering and oxidation and recovery was very poor. Lithologic descriptions of the cores and cuttings for holes 9-1, 7-11, and 3-1 are listed on pages 13-21. Calculationdbased on hole 9-1 indicate that of the total lignite zone, 56 percent consists of partings and 44 percent is lignite. These percentages were obtained by statistical analysis of the core description and natural gamma logs of the hole. The total thickness of the lignite zone in hole 9-1 is approximately 18 m.

Colorado↗
USGS1977

Mineralogical, chemical, and physical properties of the regolith overlying crystalline rocks, Fairfax County, Virginia: a preliminary report

Undisturbed cores of saprolite developed on crystalline rocks of the Piedmont Province in Fairfax County, Virginia have been obtained using a combination of Shelby tubes, Denison sampler, and modified diamond core-drilling. The principal purpose of the core study is to correlate variations in chemistry, mineralogy and texture with engineering properties throughout the weathering profile. Coring sites were chosen to obtain a maximum depth of weathering on diverse lithologies. The rocks investigated include pelitic schist, metagraywacke, granite, diabase and serpentinite. Four to twelve samples per core were selected, depending on thickness of 1) the weathering profile (from about 1 m in serpentinite to more than 30 m in pelitic schist) and on 2) megascopic changes in saprolite character for analysis of petrography, texture, clay mineralogy andd major element chemistry. Shear strength and compressibility were determined on corresponding segments of core. Standard penetration tests were performed adjacent to coring sites to evaluate engineering properties in situ. Geochemical changes of saprolite developed from each rock type follow predictable trends from fresh rock to soil profile, with relative Increases in Si, Ti, Al, Fe3+ and H20; variable K; and relative loss of Fe 2+, Mg, Ca, and Na. These variations are more pronounced in the weathering profiles over mafic and ultramafic rocks than metagraywacke. Clay minerals in granite, schist and metagraywacke saprolite are kaolinite, dioctahedral vermiculite, interlayered micavermiculite, and minor illite. Gibbsite is locally developed in near-surface samples of schist. Standard penetration test data for the upper 7 m of saprolite over schist and metagraywacke suggest alternations between stronger and weaker horizons than probably reflect variations in lithology including the presence of quartz lenses. Results for granite saprolite are most consistent but indicate lower strength. Shear strength increases fairly regularly downward in the weathering profile. The engineering behavior of diabase saprolite is controlled by a dense, plastic, near-surface clay layer (montmorillonite and kaolinite)overlying rock which is weathered to a granular state (grus), while engineering properties of serpentinite are determined by a very thin weathering profile.

Open-File Report↗