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At least 1,441 records · Page 80Linked to original sources
USGS1998

U.S. Geological Survey cooperative water-resources programs in Chester County, Pennsylvania

Since 1969, the U.S. Geological Survey (USGS) has had a cooperative water-resources investigation program with Chester County to measure and describe the water resources of the County. Generally, the USGS provides one-half of the program funding, and local cooperators are required to provide matching funds. Cooperation has been primarily with the Chester County Water Resources Authority (CCWRA), with participation from the Chester County Health Department and funding from the Chester County Board of Commissioners. Municipalities and the Red Clay Valley Association also have provided part of the funding for several projects. This report describes how the long-term partnership between the USGS and Chester County, Pa., provides the County with the information that it needs for sound water-resources management. The CCWRA was created in 1961, primarily for land acquisition and planning for flood-control and water-supply projects. With the backing of the Brandywine Valley Association, the CCWRA started its first cooperative project with the USGS in 1969. It was a study of the water-quality condition of Chester County streams with an emphasis on benthic macroinvertebrates and stream chemistry. The kinds of projects and data collection conducted by the USGS have changed with the needs of Chester County and the mission of the CCWRA. Chester County is experiencing rapid population growth (it had the tenth-highest rate of growth in the nation from 1980 to 1990). This growth places considerable stress on water resources and has caused the CCWRA to broaden its focus from flood control to water-supply planning, water quality, and ground-water and surface-water management. The results of USGS studies are used by the CCWRA and other County agencies, including the Planning Commission, Health Department, and Parks and Recreation Department, for conducting day-to-day activities and planning for future growth. The results also are used by the CCWRA to provide guidance and technical assistance to municipalities, water suppliers, industrial dischargers, watershed and conservancy associations and other civic organizations, state and Federal agencies, river basin commissions, and the private sector. The cooperative water-resources program, which is described in the following sections, benefits not only the citizens of Chester County but also serves the interests of the Federal Government. Innovative studies conducted in Chester County provide methods and interpretations that often can be used nationwide, and the headwaters of several interstate drainages lie within the County. Major program thrusts include collection of surface-water, ground-water, and water-quality data and interpretive studies. The use of this information also is described.

Pennsylvania↗
USGS1990

Modelling streamwater chemistry as a mixture of soilwater end-members - A step towards second-generation acidification models

In present acidification models, soilwater characteristics, though modelled, are seldom checked against field observations. Given that such data are now collected as part of many catchment studies, a technique is developed whereby stream water can be predicted as a mixture of the observed soilwater classes or end-members. Provided that a sufficient set of end-members has been identified, a least-squares technique can be used to estimate the contribution to the stream from each end-member, whenever streamwater samples have been taken. For two catchments, Birkenes in southern Norway and Plynlimon in Mid-Wales, the analysis indicates that the soilwater end-members observed to date are insufficient to explain streamwater chemistry. However, properties of the missing soil waters have been identified, thus facilitating future field work. When an adequate set of soilwater end-members has been established, long-term predictions of changes in streamwater chemistry reduce to the problem of predicting the fate of each end-member. Thus, a separate hydrological submodel is not needed, since the mixing patterns are derived from the end-member analysis.

Journal of Hydrology↗
USGS1985

Chemistry of thermal and nonthermal springs in the vicinity of Lassen Volcanic National Park

Meaningful applications of water geothermometry to thermal springs in and around Lassen Volcanic National Park (LVNP) are limited to Growler Hot Spring and Morgan Hot Springs. Most hot springs located within LVNP are low-chloride, acid-sulfate waters associated with nearby steam vents. This type of hot-spring activity is characteristically found above vapor-dominated hydrothermal systems. These acid-sulfate waters are not generally useful for liquid chemical geothermometry, however, because their chemical compositions result from water-rock interaction at relatively shallow depths. Thermal waters at Drakesbad and in Little Hot Springs Valley have neutral-pH, low-Cl concentrations and have estimated Na-K-Ca and Na-Li geothermometer temperatures close to measured spring temperatures of 65 to 95??C. Hot-spring waters located south of LVNP at Growler Hot Spring, Morgan Hot Springs, and in the south-central part of LVNP in the Walker "O" No. 1 well at Terminal Geyser are rich in chloride and yield calculated geothermometer temperatures between 220 and 230??C. These thermal waters probably originate within a zone of upflow of high-enthalpy fluid inside LVNP and cool conductively during lateral flow to the south and southeast. ?? 1985.

Journal of Volcanology and Geothermal Research↗
USGS2018

Changes in long-term water quality of Baltimore streams are associated with both gray and green infrastructure

The steadily rising global urban population has placed substantial strain on urban water quality, and this strain is projected to increase for the foreseeable future. Considerable attention has been given to the hydrological and physico-chemical effects of urbanization on stream ecosystems. However, due to the relative infancy of the field of urban ecology, long-term water quality analyses in urban streams are sparse. Using a 15-year stream chemistry monitoring record from Baltimore, MD, USA, we quantified long-term trends in nitrate, phosphate, total nitrogen, total phosphorus, chloride, and sulfate export at several sites along a rural-urban gradient. We found no significant change in solute export at most sites, although we did find specific patterns of interest for certain solutes. For example, nitrogen export declined at the most headwater urban site, while phosphorus export declined at the most downstream urban site. Coupling long-term monitoring with data on gray and green infrastructure management throughout the landscape, we established relationships between solute export at the most downstream urban monitoring site and sanitary sewer overflows (SSOs), best management practice (BMP) implementation, and road salt application rates. Phosphorus export was correlated with BMP implementation in the watershed, whereas nitrogen export was related to SSOs. Despite highly urbanized watersheds, water quality does not appear to be declining at most of these sites, suggesting that current management may have limited further impairment. Results of our study suggest that both gray and green infrastructure are key for maintaining and improving water quality in this highly urbanized watershed.

Maryland↗
USGS1987

Ground-water and soil contamination near two pesticide-burial sites in Minnesota

Preliminary investigations of the geology, groundwater hydrology , and soil and groundwater chemistry at sites in Pine and St. Louis Counties, Minnesota, have shown that contamination associated with pesticides buried at the sites is not widespread or highly concentrated. None of the pesticides sampled for in soil and in groundwater at the sites exceeded Minnesota soil and drinking water standards. About 1,500 pounds of lead arsenate were buried at the site in St. Louis County. Nearly 10,000 pounds of lead arsenate, as well as smaller quantities of organic pesticides (such as chlorpropham, DDT, endrin, and aldrin), lime sulfur, and magnesium carbonate were buried at the Pine County site. These chemicals were buried in shallow trenches at the sites during the early 1970's. The first wells drilled at each site were located to establish the direction of horizontal groundwater flow in each area. Groundwater flows to the northeast at the St. Louis County site and to the southeast at the Pine County site. Depths to the water table are about 30 ft at the Pine County site and about 25 ft at the St. Louis County site. In addition, groundwater is perched seasonally at about 5 ft below land surface in the immediate vicinity fo the burial site in Pine County. After the direction of flow was determined, additional wells were drilled down-gradient from the disposal areas at both sites to determine whether contaminations were migrating with groundwater away from the sites. In general, concentrations of lead and arsenic in soil and groundwater were below background concentrations for the areas. Concentrations of organic pesticides generally were below analytical-detection limits. The limited solubility of the chemicals and the tendency of the contaminants to be sorbed on soil particles probably combined to restrict mobilization of the chemicals.

Minnesota↗
USGS2015

Water resources during drought conditions and postfire water quality in the upper Rio Hondo Basin, Lincoln County, New Mexico, 2010-13

Stakeholders and water-resource managers in Lincoln County, New Mexico, have had long-standing concerns over the impact of population growth and groundwater withdrawals. These concerns have been exacerbated in recent years by extreme drought conditions and two major wildfires in the upper Rio Hondo Basin, located in south-central New Mexico. The U.S. Geological Survey (USGS), in cooperation with Lincoln County, initiated a study in 2006 to assess and characterize water resources in the upper Rio Hondo Basin. Data collected during water years 2010–13 are presented and interpreted in this report. All data presented in this report are described in water years unless stated otherwise. Annual mean streamflow at the Rio Ruidoso at Hollywood, N. Mex., streamflow-gaging station was less than 50 percent of the average streamflow during 2011–13 and was of similar magnitude to annual mean streamflow values measured during the drought of the 1950s. The first zero-streamflow values for the period of record (1954–2013) were recorded at the Rio Ruidoso at Hollywood, N. Mex., streamflow-gaging station on June 27–29, 2013. The lowest annual mean streamflow on record (1969–80; 1988–2013) occurred in 2011 at the Eagle Creek below South Fork near Alto, N. Mex., streamflow-gaging station, with the station recording zero streamflow for approximately 50 percent of the year. Discrete and continuous groundwater-level measurements indicated basinwide water-level declines during drought conditions in 2011–13. The average water-level change among 37 wells in which discrete groundwater-level measurements were collected was -7.6 ft from 2010 to 2013. The largest water-level declines were observed in the upper reaches of the Rio Bonito and Rio Ruidoso watersheds, and smaller declines were observed in the lower reaches of the watersheds. In general, water-level changes observed during 2010–13 were on the order of decadal-scale changes that previously have been observed in the upper Rio Hondo Basin. Stable-isotope data indicate that high-elevation winter precipitation generally contributes more to groundwater recharge than summer rains, except when there are large summer recharge events. This implies that little recharge is occurring at the lower elevations in the upper Rio Hondo Basin because these areas receive a smaller amount of total precipitation, receive a smaller proportion of the annual total falling as winter precipitation, and have higher average temperatures that result in more evaporative losses. Groundwater in the upper Rio Hondo Basin is a mix of younger and older water, and recharge likely is occurring primarily at higher elevations but there may be some areas where localized recharge is occurring at lower elevations. Surface-water- and groundwater-quality results from samples collected in 2012–13 were examined to characterize overall chemistry and were compared to historical waterquality data from streams in the upper Rio Hondo Basin collected during 1926–57. In general, specific conductance showed an increasing trend moving eastward (downstream) through the upper Rio Hondo Basin in surface-water and groundwater samples. Surface-water and groundwater samples appear to have similar overall major-ion chemical characteristics when compared to historical water-quality data. Geology was found to influence the chemical characteristics of surface-water and groundwater samples, with relatively higher concentrations of sulfate occurring in samples collected at lower elevations in the Permian regional aquifer system. Surface-water sample results also were analyzed to determine differences in unfiltered and filtered water-quality samples of streams in burned and unburned watersheds after the occurrence of the Little Bear Fire in June 2012. Samples were collected after postfire monsoon rain events and during periods of stable hydrologic conditions. The first postfire monsoon rain event in July 2012 generally produced the highest measured concentrations of selected fire-related constituents in unfiltered samples collected in the burned watersheds relative to later samples collected in burned watersheds and all samples collected in the unburned watershed. Monsoon rain events have impacted water quality by delivering larger sediment loads and fire-related constituents into streams in the upper Rio Hondo Basin. Changes in climate and increased groundwater and surface-water use are likely to affect the availability of water in the upper Rio Hondo Basin. Increased drought probably will increase the potential for wildfires, which can affect downstream water quality and increase flood potential. Climate-research predicted decreases in winter precipitation may have an adverse effect on the amount of groundwater recharge that occurs in the upper Rio Hondo Basin, given the predominance of winter precipitation recharge as indicated by the stable isotope results. Decreases in surface-water supplies because of persistent drought conditions and reductions in the quality of water because of the effects of wildfire may lead to a larger reliance on groundwater reserves in the upper Rio Hondo Basin. Decreasing water levels because of increasing groundwater withdrawal could reduce base flows in the Rio Bonito and Rio Ruidoso. Well organized and scientifically supported regional water-resources management will be necessary for dealing with the likely scenario of increases in demand coupled with decreases in supply in the upper Rio Hondo Basin.

New Mexico↗
USGS1997

The relationship between land use and organochlorine compounds in streambed sediment and fish in the Central Columbia Plateau, Washington and Idaho, USA

We analyzeds streambed sediment and fish in the Central Columbia Plateau in eastern Washington and Idaho for or ganochlorine pesticides and polychlorinated biphenyls (ΣPCB). Our objective was to assess the effects of land use on the occurrence and distribution of these compounds; land uses in the study area included forest, dryland and irrigated farming, and urban. We detected 16 organochlorine compounds in streambed sediment and fish tissue; fish usually had more compounds and a greater frequency of detection. The most frequently detected compound was ΣDDT (sum of six isomers), which was found in 52% of bed sediment samples and 94% of whole fish composite samples. The other commonly detected compounds were dimethyl tetrachloroterephthalate (DCPA), dieldrin, hexachlorobenzene, and Σchlordane (sum of cis - and trans -chlordane, cis - and trans -nonachlor oxychlordane, heptachlor, and heptachlor epoxide). Forest was the only land use with no detections of organochlorine compounds in either fish or bed sediment. Hexachlorobenzene was the only organochlorine pesticide detected at concentrations that differed significantly among land uses: concentrations were higher in the dryland farming areas than in the irrigated farming or urban areas. In agricultural areas irrigated by surface water, ΣDDT concentrations in both streambed sediment and fish tissue were related to the percentage of land irrigated by water delivered via furrows (gravity irrigation), although ΣDDT was not detectable in bed sediments until gravity irrigation exceeded 30%. Because of the relation between gravity irrigation and soil erosion, our study supports the importance of controlling soil erosion in order to reduce the overall loading of organochlorine compounds to surface waters.

Environmental Toxicology and Chemistry↗
USGS2024

Riverine dissolved organic matter transformations increase with watershed area, water residence time, and Damköhler numbers in nested watersheds

Quantifying the relative influence of factors and processes controlling riverine ecosystem function is essential to predicting future conditions under global change. Dissolved organic matter (DOM) is a fundamental component of riverine ecosystems that fuels microbial food webs, influences nutrient and light availability, and represents a significant carbon flux globally. The heterogeneous nature of DOM molecular composition and its propensity for interaction (i.e., functional diversity) can characterize riverine ecosystem function across spatiotemporal scales. To investigate fundamental drivers of DOM diversity, we collected seasonal water samples from 42 nested locations within five watersheds spanning multiple watershed sizes (~5 to 30,000 km2) across the United States. Patterns in DOM molecular richness, aromaticity, relative abundance of N-containing formulas, and putative biochemical transformations derived from high-resolution mass spectrometry were assessed across gradients of explanatory variables associated with watershed characteristics (e.g., watershed area, water residence time, land cover). We found that putative biochemical transformations were more strongly related to explanatory variables across watersheds than common bulk DOM parameters and that watershed area, surface water residence time and derived Damköhler numbers representing DOM reactivity timescales were strong predictors of DOM diversity. The data also indicate that catchment-specific land cover factors can significantly influence DOM diversity in diverging directions. Overall, the results highlight the importance of considering water residence time and land cover when interpreting longitudinal patterns in DOM chemistry and the continued challenge of identifying generalizable drivers that are transferable across watershed and regional scales for application in Earth system models. This work also introduces a Findable Accessible Interoperable Reusable (FAIR) dataset (>300 samples) to the community for future syntheses.

Biogeochemistry↗
USGS1996

Organic geochemistry applied to environmental assessments of Prince William Sound, Alaska, after the Exxon Valdez oil spill—a review

Organic geochemistry played a major role in the environmental assessments conducted following the Exxon Valdez oil spill, which occurred on March 24, 1989, and released about 258,000 bbls (41 million liters) of Alaska North Slope crude oil into Prince William Sound. Geochemical analyses of more than 15,000 sediment, tar, and biological samples and about 5000 water samples provide the largest database yet collected on oil-spill chemistry, and we review the results here. The marine environment of the Sound has a complex background of petrogenic, pyrogenic, and biogenic hydrocarbons from natural and anthropogenic sources. Geochemical evaluation of the fate and effects of the spilled oil required that this oil and its residues be distinguished from the background. A variety of molecular and isotopic techniques were employed to identify various hydrocarbon sources and to distinguish quantitatively among mixed sources in the samples. Although the specific criteria used to distinguish multiple sources in the region affected by the Exxon Valdez spill are not necessarily applicable to all spill situations, the principles that governed their selection are. Distributions of polycyclic aromatic hydrocarbons (PAH) and dibenzothiophenes distinguish Exxon Valdez oil and its weathered residues from background hydrocarbons in benthic sediments. Ratios of C 2 -dibenzothiophene C 2 -phenanthrene "> C 2 -dibenzothiopheneC 2 -phenanthrene and C 3 -dibenzothiophene C 3 -phenanthrene "> C 3 -dibenzothiopheneC 3 -phenanthrene were particularly useful. Carbon isotopes and terpane distributions distinguished Exxon Valdez residues found on shorelines from tars from other sources. Diesel and diesel soot were identified by the absence of alkylated chrysenes and a narrow distribution of n -alkanes, whereas pyrogenic products were distinguished by the dominance of 4- to 6-ring PAH over 2- to 3-ring PAH and by the dominance of non-alkylated over alkylated homologues of each PAH series. The presence of 18α(H)-oleanane in benthic sediments, coupled with its absence in Exxon Valdez oil and its residues, confirm another petrogenic source. Results of geochemical studies suggest that the petrogenic component in the background of benthic sediments is derived from oil seeps in the eastern Gulf of Alaska. In 1990 and 1991, Exxon Valdez residues, generally forming a small increment to the pre-spill background, were found to be only sporadically distributed in some shallow, near shore sediments adjacent to shorelines that had been heavily oiled in 1989. In 1994, occurrences of Exxon Valdez tars on shoreline surfaces were rare, although residues could be found buried in shoreline sediments at some isolated locations along the spill path where they were protected from wave action. Spilled oil residues collected 16 months after the spill were degraded, on average, by nearly 50%. Shoreline residues from sources other than the spill were also identified and are widespread throughout the Sound. These residues include (1) geochemically distinct tars and oils imported from California oil fields to Alaska for fuel and construction purposes prior to the discovery of the Cook Inlet and North Slope oil fields, (2) diesel and diesel soot, and (3) more highly refined products. Of the more than 2700 chemical analyses of biological samples of higher life forms (fish, birds, and mammals) about 150 (6%) indicate recognizable residues of Exxon Valdez oil, which were identified by their distribution of polycyclic aromatic hydrocarbons (PAH). Most of these samples (138) were collected in 1989 and most were associated with external surfaces or the gastrointestinal tract. Rarely do internal tissues or fluids contain recognizable fingerprints of spilled oil. This observation includes samples from marine mammals that were visibly oiled externally. Other hydrocarbon sources, including diesel and a non-petroleum artifact that occurs when concentrations of individual PAH are at or near their method detection limit, are also identified in biological samples.

Alaska↗
USGS2009

Diffuse gas emissions at the Ukinrek Maars, Alaska: Implications for magmatic degassing and volcanic monitoring

Diffuse CO2 efflux near the Ukinrek Maars, two small volcanic craters that formed in 1977 in a remote part of the Alaska Peninsula, was investigated using accumulation chamber measurements. High CO2 efflux, in many places exceeding 1000 g m−2 d−1, was found in conspicuous zones of plant damage or kill that cover 30,000–50,000 m2 in area. Total diffuse CO2 emission was estimated at 21–44 t d−1. Gas vents 3-km away at The Gas Rocks produce 0.5 t d−1 of CO2 that probably derives from the Ukinrek Maars basalt based on similar δ13C values (∼−6‰), 3He/4He ratios (5.9–7.2 RA), and CO2/3He ratios (1–2 × 109) in the two areas. A lower 3He/4He ratio (2.7 RA) and much higher CO2/3He ratio (9 × 1010) in gas from the nearest arc-front volcanic center (Mount Peulik/Ugashik) provide a useful comparison. The large diffuse CO2 emission at Ukinrek has important implications for magmatic degassing, subsurface gas transport, and local toxicity hazards. Gas–water–rock interactions play a major role in the location, magnitude and chemistry of the emissions.

Alaska↗
USGS2011

Strong atmospheric chemistry feedback to climate warming from Arctic methane emissions

The magnitude and feedbacks of future methane release from the Arctic region are unknown. Despite limited documentation of potential future releases associated with thawing permafrost and degassing methane hydrates, the large potential for future methane releases calls for improved understanding of the interaction of a changing climate with processes in the Arctic and chemical feedbacks in the atmosphere. Here we apply a “state of the art” atmospheric chemistry transport model to show that large emissions of CH4 would likely have an unexpectedly large impact on the chemical composition of the atmosphere and on radiative forcing (RF). The indirect contribution to RF of additional methane emission is particularly important. It is shown that if global methane emissions were to increase by factors of 2.5 and 5.2 above current emissions, the indirect contributions to RF would be about 250% and 400%, respectively, of the RF that can be attributed to directly emitted methane alone. Assuming several hypothetical scenarios of CH4 release associated with permafrost thaw, shallow marine hydrate degassing, and submarine landslides, we find a strong positive feedback on RF through atmospheric chemistry. In particular, the impact of CH4 is enhanced through increase of its lifetime, and of atmospheric abundances of ozone, stratospheric water vapor, and CO2 as a result of atmospheric chemical processes. Despite uncertainties in emission scenarios, our results provide a better understanding of the feedbacks in the atmospheric chemistry that would amplify climate warming.

Global Biogeochemical Cycles↗
USGS2003

Identifying relationships between baseflow geochemistry and land use with synoptic sampling and R-mode factor analysis

The relationship between land use and stream chemistry is often explored through synoptic sampling of rivers at baseflow conditions. However, baseflow chemistry is likely to vary temporally and spatially with land use. The purpose of our study is to examine the usefulness of the synoptic sampling approach for identifying the relationship between complex land use configurations and stream water quality. This study compares biogeochemical data from three synoptic sampling events representing the temporal variability of baseflow chemistry and land use using R - mode factor analysis . Separate R - mode factor analyses of the data from individual sampling events yielded only two consistent factors. Agricultural activity was associated with elevated levels of Ca 2+ , Mg 2+ , alkalinity, and frequently K + , SO 2- 4 , and NO - 3 . Urban areas were associated with higher concentrations of Na + , K + , and Cl - . Other retained factors were not consistent among sampling events, and some factors were difficult to interpret in the context of biogeochemical sources and processes. When all data were combined, further associations were revealed such as an inverse relationship between the proportion of wetlands and stream nitrate concentrations. We also found that barren lands were associated with elevated sulfate levels. This research suggests that an individual sampling event is unlikely to characterize adequately the complex processes controlling interactions between land use and stream chemistry. Combining data collected over two years during three synoptic sampling events appears to enhance our ability to understand processes linking stream chemistry and land use.

Michigan↗
USGS1989

Humic substances in the Suwannee River, Georgia; interactions, properties, and proposed structures

Humic substances as a collective term and humic and fulvic acids as specific terms are not household words. For about a century, these terms belonged to the domain of the soil scientist. Even^though their chemical structures remained elusive, they were recognized as important entities in soil. During the past decade or so, there has been a renewed interest in humic substances in soil and water. Such interest has been the result of improved analytical instrumentation, and by a need to understand the structure and function of natural organic substances in water. A responsibility of the U.S. Geological Survey is to assess the Nation's water resources; this includes water quality, which is the study of material in water. Such material may be suspended, colloidal, or in true solution. Because humic substances are a major carbon source in water, they have received attention by Geological Survey scientists. This attention has been a major focus by members of the Geological Survey's organic-chemistry group. For more than a decade, this group has collected samples, made analyses, and worked toward determining the structures and function of humic substances in water. Their work has brought worldwide recognition to the field, and in 1981, through Geological Survey support, they helped organize the International Humic Substances Society, which held its first meeting in Estes Park, Colorado, in August 1983. At the second meeting of the Society in Birmingham, England, in August 1984, it became apparent that Geological Survey scientists were rapidly advancing the study of the chemistry of humic substances. It seemed appropriate, therefore, to publish this Open-File report on humic and fulvic acids from the Suwannee River in Georgia. The results represent our most definitive findings to date (1986). Though this work is not conclusive, it is state-of-the-science. Hopefully, our reporting on this work will aid in moving the science of humic substances forward as others read of our progress, findings, and theories. If so, this Open-File report will have served its purpose.

Georgia↗
USGS2016

Increasing aeolian dust deposition to snowpacks in the Rocky Mountains inferred from snowpack, wet deposition, and aerosol chemistry

Mountain snowpacks are a vital natural resource for ∼1.5 billion people in the northern Hemisphere, helping to meet human and ecological demand for water in excess of that provided by summer rain. Springtime warming and aeolian dust deposition accelerate snowmelt, increasing the risk of water shortages during late summer, when demand is greatest. While climate networks provide data that can be used to evaluate the effect of warming on snowpack resources, there are no established regional networks for monitoring aeolian dust deposition to snow. In this study, we test the hypothesis that chemistry of snow, wet deposition, and aerosols can be used as a surrogate for dust deposition to snow. We then analyze spatial patterns and temporal trends in inferred springtime dust deposition to snow across the Rocky Mountains, USA, for 1993–2014. Geochemical evidence, including strong correlations (r 2 ≥ 0.94) between Ca 2+ , alkalinity, and dust concentrations in snow deposited during dust events, indicate that carbonate minerals in dust impart a strong chemical signature that can be used to track dust deposition to snow. Spatial patterns in chemistry of snow, wet deposition, and aerosols indicate that dust deposition increases from north to south in the Rocky Mountains, and temporal trends indicate that winter/spring dust deposition increased by 81% in the southern Rockies during 1993–2014. Using a multivariate modeling approach, we determined that increases in dust deposition and decreases in springtime snowfall combined to accelerate snowmelt timing in the southern Rockies by approximately 7–18 days between 1993 and 2014. Previous studies have shown that aeolian dust emissions may have doubled globally during the 20th century, possibly due to drought and land-use change. Climate projections for increased aridity in the southwestern U.S., northern Africa, and other mid-latitude regions of the northern Hemisphere suggest that aeolian dust emissions may continue to increase, compounding the risk that climate warming poses to snowpack water resources in arid/semi-arid regions of the world.

Atmospheric Environment↗
USGS2001

National Water Quality Laboratory - A profile

The U.S. Geological Survey (USGS) National Water Quality Laboratory (NWQL) is a full-service laboratory that specializes in environmental analytical chemistry. The NWQL's primary mission is to support USGS programs requiring environmental analyses that provide consistent methodology for national assessment and trends analysis. The NWQL provides the following: high-quality chemical data; consistent, published, state-of-the-art methodology; extremely low-detection levels; high-volume capability; biological unit for identifying benthic invertebrates; quality assurance for determining long-term water-quality trends; and a professional staff.

Fact Sheet↗
USGS1999

Lanthanide, yttrium, and zirconium anomalies in the Fire Clay coal bed, Eastern Kentucky

The Fire Clay coal bed in the Central Appalachian basin region contains a laterally-persistent tonstein that is found in the coal throughout most of its areal extent. The tonstein contains an array of minerals, including sanidine, ??-quartz, anatase and euhedral zircon, thhat constitutes strong evidence for a volcanic origin of the parting. For this study, five samples of the tonstein and four sets of coal samples underlying the tonstein were collected from five sites in eastern Kentucky. Inductively coupled plasma-mass spectroscopy (ICP-MS) analysis of the tonstein and underlying coal collected from four sites in eastern Kentucky show that although Zr concentrations are high in the tonstein (570-1820 ppm on a coal-ash basis (cab)), they are highest in the coal directly underlying the tonstein (2870-4540 ppm (cab)). A similar enrichment pattern is observed in the concentration of Y plus the sum of the rare earth elements (Y + ??REE): total Y + ??REE concentrations in the five tonstein samples range from 511 to 565 ppm (cab). However, Y + ??REE contents are highest in the coals directly underlying the tonsteins: values range from 1965 to 4198 ppm (cab). Scanning electron microscopy of samples from coal which directly underlies two of the tonstein samples show that REE-rich phosphate, tentatively identified as monazite, commonly infills cracks in clays and cells in clarain and vitrain. Zircon is rare and commonly subhedral. On the basis of coal chemistry and grain morphology, we suggest that volcanic components in the tonstein were leached by ground water. The leachate, rich in Y and REE precipitated as authigenic mineral phases in the underlying coal.The Fire Clay coal bed in the Central Appalachian basin region contains a laterally-persistent tonstein that is found in the coal throughout most of its areal extent. The tonstein contains an array of minerals, including sanidine, ??-quartz, anatase and euhedral zircon, that constitutes strong evidence for a volcanic origin of the parting. For this study, five samples of the tonstein and four sets of coal samples underlying the tonstein were collected from five sites in eastern Kentucky. Inductively coupled plasma-mass spectroscopy (ICP-MS) analysis of the tonstein and underlying coal collected from four sites in eastern Kentucky show that although Zr concentrations are high in the tonstein (570-1820 ppm on a coal-ash basis (cab)), they are highest in the coal directly underlying the tonstein (2870-4540 ppm (cab)). A similar enrichment pattern is observed in the concentration of Y plus the sum of the rare earth elements (Y+???REE): total Y+???REE concentrations in the five tonstein samples range from 511 to 565 ppm (cab). However, Y+???REE contents are highest in the coals directly underlying the tonsteins: values range from 1965 to 4198 ppm (cab). Scanning electron microscopy of samples from coal which directly underlies two of the tonstein samples show that REE-rich phosphate, tentatively identified as monazite, commonly infills cracks in clays and cells in clarain and vitrain. Zircon is rare and commonly subhedral. On the basis of coal chemistry and grain morphology, we suggest that volcanic components in the tonstein were leached by ground water. The leachate, rich in Y and REE precipitated as authigenic mineral phases in the underlying coal.

International Journal of Coal Geology↗
USGS2007

Questions and Answers About the Effects of Septic Systems on Water Quality in the La Pine Area, Oregon

Nitrate levels in the ground-water aquifer underlying the central Oregon city of La Pine and the surrounding area are increasing due to contamination from residential septic systems. This contamination has public health implications because ground water is the sole source of drinking water for area residents. The U.S. Geological Survey, in cooperation with Deschutes County and the Oregon Department of Environmental Quality, studied the movement and chemistry of nitrate in the aquifer and developed computer models that can be used to predict future nitrate levels and to evaluate alternatives for protecting water quality. This fact sheet summarizes the results of that study in the form of questions and answers.

Fact Sheet↗