Geology topics

M. Alisa Mast

Publications and source records attributed to M. Alisa Mast.

At least 55 records · Page 3Linked to original sources

USGS2011

Trends in lake chemistry in response to atmospheric deposition and climate in selected Class I wilderness areas in Colorado, Idaho, Utah, and Wyoming, 1993-2009

In 2010, the U.S. Geological Survey, in cooperation with the U.S. Department of Agriculture Forest Service, Air Resource Management, began a study to evaluate long-term trends in lake-water chemistry for 64 high-elevation lakes in selected Class I wilderness areas in Colorado, Idaho, Utah, and Wyoming during 1993 to 2009. The purpose of this report is to describe trends in the chemical composition of these high-elevation lakes. Trends in emissions, atmospheric deposition, and climate variables (air temperature and precipitation amount) are evaluated over a similar period of record to determine likely drivers of changing lake chemistry. Sulfate concentrations in precipitation decreased over the past two decades at high-elevation monitoring stations in the Rocky Mountain region. The trend in deposition chemistry is consistent with regional declines in sulfur dioxide emissions resulting from installation of emission controls at large stationary sources. Trends in nitrogen deposition were not as widespread as those for sulfate. About one-half of monitoring stations showed increases in ammonium concentrations, but few showed significant changes in nitrate concentrations. Trends in nitrogen deposition appear to be inconsistent with available emission inventories, which indicate modest declines in nitrogen emissions in the Rocky Mountain region since the mid-1990s. This discrepancy may reflect uncertainties in emission inventories or changes in atmospheric transformations of nitrogen species that may be affecting deposition processes. Analysis of long-term climate records indicates that average annual mean air temperature minimums have increased from 0.57 to 0.75 °C per decade in mountain areas of the region with warming trends being more pronounced in Colorado. Trends in annual precipitation were not evident over the period 1990 to 2006, although wetter than average years during 1995 to 1997 and drier years during 2001 to 2004 caused a notable decline in precipitation in the middle part of the record.

Colorado;Idaho;Utah;Wyoming↗

USGS2011

Potential climate change effects on water tables and pyrite oxidation in headwater catchments in Colorado

A water, energy, and biogeochemical model (WEBMOD) was constructed to simulate hydrology and pyrite oxidation for the period October 1992 through September 1997. The hydrologic model simulates processes in Loch Vale, a 6.6-km² granitic watershed that drains the east side of the Continental Divide. Parameters describing pyrite oxidation were derived sulfate concentrations measured in pore water and stream water in Handcart Gulch, a naturally acidic watershed in the Colorado Mineral Belt. Average monthly differences in precipitation and temperature between current and future climates, as predicted by using six global circulation models and three carbondioxide emission scenarios, were input into WEBMOD to identify possible shifts in the quantity and quality of the water flowing from the watershed for the period 2005 through 2100. Initial results suggest that increased air temperatures will result in earlier snowmelt compared to current conditions. Average sulfate concentrations and acidity in streams draining hydrothermally altered terrain may decrease as water tables rise in response to greater overall precipitation and earlier snowmelt, although a net increase of sulfate load was simulated as a result of greater overall discharge. Evapotranspiration is expected to increase but not enough to offset the increase in precipitation.

Colorado↗

USGS2010

Processes controlling the chemistry of two snowmelt‐dominated streams in the Rocky Mountains

Time‐intensive discharge and chemical data for two alpine streams in the Loch Vale watershed, Colorado, were used to identify sources of runoff, flow paths, and important biogeochemical processes during the 1992 snowmelt runoff season. In spite of the paucity of soil cover the chemical composition of the streams is regulated much as in typical forested watersheds. Soils and other shallow groundwater matrices such as boulder fields appear to be more important in controlling surface‐water chemistry than their abundance would indicate. The chemical composition of the major source waters (usually thought of as end‐members whose chemical composition is relatively constant over time) changes at the same time that their mixing ratio in streams changes, confounding use of end‐member mixing models to describe stream‐water chemistry. Changes in the chemical composition of these source waters are caused by the ionic pulse of solutes from the snowpack and the small size of the shallow groundwater reservoir compared to the volume of snowmelt passing through it. The brief hydrologic residence time in the shallow groundwater indicates that concentrations of most dissolved constituents of stream water were controlled by fast geochemical processes that occurred on timescales of hours to days, rather than slower processes such as weathering of primary minerals. Differences in the timing of snowmelt‐related processes between different areas of the watershed also affect the stream‐water chemical composition. Cirque lakes affect discharge and chemical composition of one of the streams; seasonal control on stream‐water NO 3 and SiO 2 concentrations by diatom uptake in the lakes was inferred. Elution of acidic waters from the snowpack, along with dilution of base cations originating in shallow groundwater, caused episodes of decreased acid‐neutralizing capacity in the streams, but the streams did not become acidic.

Colorado↗

USGS2010

Chemical weathering in the Loch Vale Watershed, Rocky Mountain National Park, Colorado

Mineralogic, hydrologic, and geochemical data were used to determine the source of solutes to surface waters draining the Loch Vale Watershed (LVWS), an alpine-subalpine drainage located in the Front Range of Colorado. The flux of dissolved solids from LVWS is primarily controlled by interactions between snowmelt and materials derived from the local bedrock; the biomass has only a minor effect on solute budgets except for ammonium. LVWS is underlain by Precambrian granite and gneiss, the major minerals include quartz, microcline, plagioclase, biotite, and sillimanite. Small amounts of calcite were found along hydrothermally altered zones in the bedrock. Mass balance calculations indicate that the weathering of calcite contributes nearly 40% of the cations derived within the basin. The importance of calcite weathering in LVWS is a result of its chemical reactivity and the high rate of physical erosion in this alpine environment. The average cationic denudation rate in the drainage (390 eq/ha/yr) is similar to long-term rates in forested Adirondack watersheds (500–600 eq/ha/yr), but much lower than the average for the North American Continent (3800 eq/ha/yr). Surface waters in LVWS are susceptible to acidification should acid deposition from the atmosphere increase.

Colorado↗

USGS2010

Response of lake chemistry to changes in atmospheric deposition and climate in three high-elevation wilderness areas of Colorado

Trends in precipitation chemistry and hydrologic and climatic data were examined as drivers of long-term changes in the chemical composition of high-elevation lakes in three wilderness areas in Colorado during 1985–2008. Sulfate concentrations in precipitation decreased at a rate of −0.15 to −0.55 μeq/l/year at 10 high-elevation National Atmospheric Deposition Program stations in the state during 1987–2008 reflecting regional reductions in SO 2 emissions. In lakes where sulfate is primarily derived from atmospheric inputs, sulfate concentrations also decreased although the rates generally were less, ranging from −0.12 to −0.27 μeq/l/year. The similarity in timing and sulfur isotopic data support the hypothesis that decreases in atmospheric deposition are driving the response of high-elevation lakes in some areas of the state. By contrast, in lakes where sulfate is derived primarily from watershed weathering sources, sulfate concentrations showed sharp increases during 1985–2008. Analysis of long-term climate records indicates that annual air temperatures have increased between 0.45 and 0.93°C per decade throughout most mountainous areas of Colorado, suggesting climate as a factor. Isotopic data reveal that sulfate in these lakes is largely derived from pyrite, which may indicate climate warming is preferentially affecting the rate of pyrite weathering.

Colorado↗

USGS2010

Historical deposition of mercury and selected trace elements to high-elevation National Parks in the Western U.S. inferred from lake-sediment cores

Atmospheric deposition of Hg and selected trace elements was reconstructed over the past 150 years using sediment cores collected from nine remote, high-elevation lakes in Rocky Mountain National Park in Colorado and Glacier National Park in Montana. Cores were age dated by 210 Pb, and sedimentation rates were determined using the constant rate of supply model. Hg concentrations in most of the cores began to increase around 1900, reaching a peak sometime after 1980. Other trace elements, particularly Pb and Cd, showed similar post-industrial increases in lake sediments, confirming that anthropogenic contaminants are reaching remote areas of the Rocky Mountains via atmospheric transport and deposition. Preindustrial (pre-1875) Hg fluxes in the sediment ranged from 5.7 to 42 μg m −2 yr −1 and modern (post-1985) fluxes ranged from 17.7 to 141 μg m −2 yr −1 . The average ratio of modern to preindustrial fluxes was 3.2, which is similar to remote lakes elsewhere in North America. Estimates of net atmospheric deposition based on the cores were 3.1 μg m −2 yr −1 for preindustrial and 11.7 μg m −2 yr −1 for modern times. Current-day measurements of wet deposition range from 5.0 to 8.6 μg m −2 yr −1 , which are lower than the modern sediment-based estimate of 11.7 μg m −2 yr −1 , perhaps owing to inputs of dry-deposited Hg to the lakes.

Atmospheric Environment↗

USGS2010

Mechanisms for chemostatic behavior in catchments: implications for CO 2 consumption by mineral weathering

Concentrations of weathering products in streams often show relatively little variation compared to changes in discharge, both at event and annual scales. In this study, several hypothesized mechanisms for this “chemostatic behavior” were evaluated, and the potential for those mechanisms to influence relations between climate, weathering fluxes, and CO 2 consumption via mineral weathering was assessed. Data from Loch Vale, an alpine catchment in the Colorado Rocky Mountains, indicates that cation exchange and seasonal precipitation and dissolution of amorphous or poorly crystalline aluminosilicates are important processes that help regulate solute concentrations in the stream; however, those processes have no direct effect on CO 2 consumption in catchments. Hydrograph separation analyses indicate that old water stored in the subsurface over the winter accounts for about one-quarter of annual streamflow, and almost one-half of annual fluxes of Na and SiO 2 in the stream; thus, flushing of old water by new water (snowmelt) is an important component of chemostatic behavior. Hydrologic flushing of subsurface materials further induces chemostatic behavior by reducing mineral saturation indices and increasing reactive mineral surface area, which stimulate mineral weathering rates. CO 2 consumption by carbonic acid mediated mineral weathering was quantified using mass-balance calculations; results indicated that silicate mineral weathering was responsible for approximately two-thirds of annual CO 2 consumption, and carbonate weathering was responsible for the remaining one-third. CO 2 consumption was strongly dependent on annual precipitation and temperature; these relations were captured in a simple statistical model that accounted for 71% of the annual variation in CO 2 consumption via mineral weathering in Loch Vale.

Colorado↗

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↗

USGS2010

Comparison of mercury in water, bottom sediment, and zooplankton in two Front Range reservoirs in Colorado, 2008-09

The U.S. Geological Survey, in cooperation with the Colorado Department of Public Health and Environment, conducted a study to investigate environmental factors that may contribute to the bioaccumulation of mercury in two Front Range reservoirs. One of the reservoirs, Brush Hollow Reservoir, currently (2009) has a fish-consumption advisory for mercury in walleye (Stizostedion vitreum), and the other, Pueblo Reservoir, which is nearby, does not. Water, bottom sediment, and zooplankton samples were collected during 2008 and 2009, and a sediment-incubation experiment was conducted in 2009. Total mercury concentrations were low in midlake water samples and were not substantially different between the two reservoirs. The only water samples with detectable methylmercury were collected in shallow areas of Brush Hollow Reservoir during spring. Mercury concentrations in reservoir bottom sediments were similar to those reported for stream sediments from unmined basins across the United States. Despite higher concentrations of fish-tissue mercury in Brush Hollow Reservoir, concentrations of methylmercury in sediment were as much as 3 times higher in Pueblo Reservoir. Mercury concentrations in zooplankton were at the low end of concentrations reported for temperate lakes in the Northeastern United States and were similar between sites, which may reflect the seasonal timing of sampling. Factors affecting bioaccumulation of mercury were assessed, including mercury sources, water quality, and reservoir characteristics. Atmospheric deposition was determined to be the dominant source of mercury; however, due to the proximity of the reservoirs, atmospheric inputs likely are similar in both study areas. Water-quality constituents commonly associated with elevated concentrations of mercury in fish (pH, alkalinity, sulfate, nutrients, and dissolved organic carbon) did not appear to explain differences in fish-tissue mercury concentrations between the reservoirs. Low methylmercury concentrations in hypolimnetic water indicate low potential for increased methylmercury production following the development of anoxic conditions in summer. Based on the limited dataset, water-level fluctuations and shoreline characteristics appear to best explain differences in fish-tissue mercury concentrations between the reservoirs. Due to the shallow depth and the large annual water-level fluctuations at Brush Hollow Reservoir, proportionally larger areas of shoreline at Brush Hollow Reservoir are subjected to annual reflooding compared to Pueblo Reservoir. Moreover, presence of macrophyte beds and regrowth of terrestrial vegetation likely increase the organic content of near-shore sediments in Brush Hollow Reservoir, which may stimulate methylmercury production in littoral areas subject to reflooding. Results of a laboratory incubation experiment were consistent with this hypothesis.

Colorado↗

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↗

USGS2009

Selected achievements, science directions, and new opportunities for the WEBB small watershed research program

Over nearly two decades, the Water, Energy, and Biogeochemical Budgets (WEBB) small watershed research program of the U.S. Geological Survey (USGS) has documented how water and solute fluxes, nutrient, carbon, and mercury dynamics, and weathering and sediment transport respond to natural and humancaused drivers, including climate, climate change, and atmospheric deposition. Together with a continued and increasing focus on the effects of climate change, more investigations are needed that examine ecological effects (e.g., evapotranspiration, nutrient uptake) and responses (e.g., species abundances, biodiversity) that are coupled with the physical and chemical processes historically observed in the WEBB program. Greater use of remote sensing, geographic modeling, and habitat/watershed modeling tools is needed, as is closer integration with the USGS-led National Phenology Network. Better understanding of process and system response times is needed. The analysis and observation of land-use and climate change effects over time should be improved by pooling data obtained by the WEBB program during the last two decades with data obtained earlier and (or) concurrently from other research and monitoring studies conducted at or near the five WEBB watershed sites. These data can be supplemented with historical and paleo-environmental information, such as could be obtained from tree rings and lake cores. Because of the relatively pristine nature and small size of its watersheds, the WEBB program could provide process understanding and basic data to better characterize and quantify ecosystem services and to develop and apply indicators of ecosystem health. In collaboration with other Federal and State watershed research programs, the WEBB program has an opportunity to contribute to tracking the short-term dynamics and long-term evolution of ecosystem services and health indicators at a multiplicity of scales across the landscape.

Conference Paper↗

USGS2008

Effects of 2003 wildfires on stream chemistry in Glacier National Park, Montana

Changes in stream chemistry were studied for 4 years following large wildfires that burned in Glacier National Park during the summer of 2003. Burned and unburned drainages were monitored from December 2003 through August 2007 for streamflow, major constituents, nutrients, and suspended sediment following the fires. Stream-water nitrate concentrations showed the greatest response to fire, increasing up to tenfold above those in the unburned drainage just prior to the first post-fire snowmelt season. Concentrations in winter base flow remained elevated during the entire study period, whereas concentrations during the growing season returned to background levels after two snowmelt seasons. Annual export of total nitrogen from the burned drainage ranged from 1·53 to 3·23 kg ha −1 yr −1 compared with 1·01 to 1·39 kg ha −1 yr −1 from the unburned drainage and exceeded atmospheric inputs for the first two post-fire water years. Fire appeared to have minimal long-term effects on other nutrients, dissolved organic carbon, and major constituents with the exception of sulfate and chloride, which showed increased concentrations for 2 years following the fire. There was little evidence that fire affected suspended-sediment concentrations in the burned drainage. Sediment yields in subalpine streams may be less affected by fire than in lower elevation streams because of the slow release rate of water during spring snowmelt.

Hydrological Processes↗

USGS2008

Presentation Showing Results of a Hydrogeochemical Investigation of the Standard Mine Vicinity, Upper Elk Creek Basin, Colorado

PREFACE This Open-File Report consists of a presentation given in Crested Butte, Colorado on December 13, 2007 to the Standard Mine Advisory Group. The presentation was paired with another presentation given by the Colorado Division of Reclamation, Mining, and Safety on the physical features and geology of the Standard Mine. The presentation in this Open-File Report summarizes the results and conclusions of a hydrogeochemical investigation of the Standard Mine performed by the U.S. Geological Survey (Manning and others, in press). The purpose of the investigation was to aid the U.S. Environmental Protection Agency in evaluating remediation options for the Standard Mine site. Additional details and supporting data related to the information in this presentation can be found in Manning and others (in press).

Open-File Report↗

USGS2008

Hydrogeochemical investigation of the Standard Mine Vicinity, Upper Elk Creek Basin, Colorado

Ground- and surface-water samples were collected in the vicinity of the Standard Mine in west-central Colorado in order to characterize the local ground-water flow system, determine metal concentrations in local ground water, and better understand factors controlling the discharge of metal-rich waters from the mine. The sampling program included a one-time sampling of springs, mine adits, and exploration pits in Elk Basin and Redwell Basin; repeated sampling throughout one year of Standard Mine Level 1 discharge and Elk Creek near its confluence with Coal Creek; and a one-time sampling of underground sites in Levels 3 and 5 of the Standard Mine. Samples were analyzed for major ions and trace elements, stable isotopes of hydrogen (2H/1H) and oxygen (18O/16O), strontium isotopes, and tritium and dissolved noble gases (including helium isotopes) for tritium/helium-3 age dating. No clear correlations were observed between natural ground-water discharge locations and map-scale faults and lithology. Surface observations and the location of ground-water discharge suggest that simple topography, rather than large-scale geologic features, primarily controls the occurrence and flow of shallow ground water in Elk Basin. Discrete inflows from cross faults or other features were not observed in Levels 3 and 5 of the Standard Mine. Instead, water entered the mine as relatively persistent dripping from gouge and breccia within the Standard fault, which both tunnels follow. Therefore, the Standard fault itself is probably the main pathway of ground-water flow from the shallow subsurface to the mine workings. Low pH (as low as 3.2) and elevated concentrations of zinc, lead, cadmium, copper, and manganese (commonly exceeding water-quality standards for Elk Creek) were measured in samples located within or immediately downgradient of areas where sulfides are abundant, including the Standard fault, the Elk Lode portal, and the breccia pipe in Redwell Basin. Concentrations of these metals were typically low and pH values were circumneutral at surrounding locations. Metal concentrations in samples collected from underground workings in the Standard Mine were also generally higher than in samples collected at aboveground sites located outside of sulfide-rich areas. Metal concentrations in discharge from the Level 1 tunnel were among the highest measured in Elk Basin. All of these observations suggest that sulfide-rich mineralized rock is the primary control on dissolved metal concentrations and pH in ground water in the Standard Mine vicinity. Waste-rock piles apparently exert another major control on metal concentrations and pH; the lowest pH and highest metal concentrations typically are found in discharge from waste-rock piles. Concentrations of several chemical constituents along with strontium isotope data indicate that none of the sampled waters could have been the primary source of metals in discharge from Level 1. Therefore, this study did not identify the primary source location for metals in Level 1 discharge. Possible sources must be located below Levels 3 and 5 or farther back into the mountainside than the ends of Levels 3 and 5. Apparent tritium/helium-3 ground-water ages ranged from 0 to 9 yr, and a considerable majority were <1 yr. Tritium data and computed initial tritium values (measured tritium plus measured tritiogenic helium-3) suggest that much of the ground water in the Standard Mine vicinity was weeks to months old rather than years old. Tritium, d2H, and d18O data from water entering into and discharging from the Standard Mine displayed spatial and temporal patterns indicating that these tracers were influenced by seasonal variations in their concentration in precipitation. The tracer data therefore suggest that ground water entering into and discharging from the Standard Mine was largely composed of water <1 yr old. Pronounced seasonal variations in geochemistry in Level 1 discharge also are consistent with short r

Colorado↗

USGS2008

Comparison of Atmospheric Deposition Among Three Sites In and Near the Flat Tops Wilderness Area, Colorado, 2003-2005

Atmospheric deposition was monitored for ammonium, nitrate, and sulfate concentrations and precipitation amounts in the Flat Tops Wilderness Area of northwestern Colorado at Ned Wilson Lake beginning in 1984 to detect changes that might result from future emissions associated with development of oil-shale resources in northwestern Colorado. Renewed monitoring, by the U.S. Geological Survey, in cooperation with Rio Blanco County, to determine the current status of atmospheric deposition has been ongoing since 2003 at Ned Wilson Lake. Two new monitoring sites were located near Ripple Creek Pass near the Flat Tops Wilderness area and about 12 kilometers north of Ned Wilson Lake because access to the area near Ripple Creek Pass is less difficult and less expensive, particularly in winter and spring. The intent of this study was to establish whether the new deposition data being collected near Ripple Creek Pass, near the northern boundary of the Flat Tops Wilderness Area, would be representative of deposition at sensitive sites within the wilderness such as Ned Wilson Lake and to compare more current (2003 through 2005) deposition data with earlier data (1984 through 1991). At Ned Wilson Lake, bulk ammonium and nitrate concentrations collected from 1984 through 1991 were similar to those from 2003 through 2005. However, in the same comparison significant differences in sulfate concentrations were observed, indicating a decrease consistent with other regional findings for similar periods. Comparison of concentrations of constituents at two bulk-deposition sites located at Ned Wilson Lake (NWLB) and near Ripple Creek Pass (RCPB) showed only one significant difference (p = 0.05) with the winter bulk nitrate concentrations for NWLB significantly lower than winter concentrations from RCPB. Another comparison of concentrations of constituents between the bulk deposition site RCPB and a wet deposition site 100 meters away (RCPW) showed no significant differences for concentrations of ammonium, nitrate, and sulfate for both the winter and summer comparisons. While results indicate many similarities in concentrations of constituents and in seasonal variability in those concentrations, they are based on a short period of study. Precipitation amounts from RCPB were less than the amounts collected at NWLB, and precipitation amounts from RCPW were less than the amounts collected at RCPB. Although RCPB may not be a perfect replacement site for NWLB, it may be similar enough to represent atmospheric deposition in areas of the Flat Tops Wilderness of northwestern Colorado.

Scientific Investigations Report↗

USGS2007

Rocky Mountain Snowpack Chemistry at Selected Sites, 2004

During spring 2004, the U.S. Geological Survey in cooperation with the National Park Service and the U.S. Department of Agriculture, Forest Service collected and analyzed snowpack samples for 65 sites in the Rocky Mountain region from New Mexico to Montana. Snowpacks were sampled from late February through early April and generally had well-below-average- to near-average snow-water equivalent. Regionally, on April 1, snow-water equivalent ranged from 50 to 89 percent. At most regional sites monitored during 1993-2004, snowpack ammonium, nitrate, and sulfate concentrations for 2004 were lower than the 12-year averages. Snowpack ammonium concentrations in the region were lower than average concentrations for the period at 61 percent of sites in the region, but showed a new pattern compared to previous years with three of the four highest 2004 concentrations observed in northern Colorado. Nitrate concentrations in 2004 were lower than the 12-year average for the year at 53 percent of regional sites, and typically occurred at sites in Wyoming, Idaho, and Montana where powerplants and large industrial areas were limited. A regional decrease in sulfate concentrations across most of the Rocky Mountains (with concentrations lower than the 12-year average at 84 percent of snowpack sites) was consistent with other monitoring of atmospheric deposition in the Western United States. Total mercury concentrations, although data are only available for the past 3 years, decreased slightly for the region as a whole in 2004 relative to 2003. Ratios of stable sulfur isotopes indicated a similar regional pattern as observed in recent years with sulfur-34 (d34S) values generally increasing northward from northern New Mexico and southern Colorado to northern Colorado, Wyoming, Idaho, and Montana.

Open-File Report↗

USGS2007

Selected water-quality data for the Standard Mine, Gunnison County, Colorado, 2006-2007

Mine drainage and underground water samples were collected for analysis of inorganic solutes as part of a 1-year, hydrogeologic investigation of the Standard Mine and vicinity. The U.S. Environmental Protection Agency has listed the Standard Mine in the Elk Creek drainage near Crested Butte, Colorado, as a Superfund Site because discharge from the Standard Mine enters Elk Creek, contributing dissolved and suspended loads of zinc, cadmium, copper, and other metals to Coal Creek, which is the primary drinking-water supply for the town of Crested Butte. Water analyses are reported for mine-effluent samples from Levels 1 and 5 of the Standard Mine, underground samples from Levels 3 and 5 of the Standard Mine, mine effluent from an adit located on the Elk Lode, and two spring samples that emerged from waste-rock material below Level 5 of the Standard Mine and the adit located on the Elk Lode. Reported analyses include field parameters (pH, specific conductance, water temperature, dissolved oxygen, and redox potential) and major constituents and trace elements.

Open-File Report↗

USGS2007

Alteration Map Showing Major Faults and Veins and Associated Water-Quality Signatures of the Animas River Watershed Headwaters Near Silverton, Southwest Colorado

This map was produced to provide hard-copy and digital data for alteration assemblages in the historical mining area centered on the Tertiary San Juan and Silverton calderas. The data have direct application to geoenvironmental and mineral exploration objectives. This dataset represents alteration mapping for the upper Animas River watershed near Silverton, Colorado. The map is based on detailed 1:12,000-scale field mapping, X-ray diffraction (XRD) analysis, mineral mapping by remote sensing (AVIRIS) data, and 1:24,000-scale aerial photographic interpretation. Geologic structures were compiled and generalized from multiple published and unpublished sources (Burbank and Luedke, 1964; Steven and others, 1974; Luedke and Burbank 1975a, b; Lipman, 1976; Luedke and Burbank, 1987; Luedke, 1996) (see Index Map). Unpublished mapping of the Ironton quadrangle by D.J. Bove and J.P. Kurtz in 1997-1999 was included.

Scientific Investigations Map↗