USGS Science⌕ Search

SEARCH · USGS Science

Results for “Environmental Chemistry”

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 1,279 records · Page 71Linked to original sources
USGS2005

Inorganic chemistry, petrography and palaeobotany of Permian coals in the Prince Charles Mountains, East Antarctica

Sampled outcrops of Permian coal seams of the Bainmedart Coal Measures in the Lambert Graben, eastern Antarctica, have been analysed for their proximates, ultimates, ash constituents and trace elements. A similar series of samples has been analysed for their principle maceral and microlithotype components and vitrinite reflectance. The coals are sub-bituminous to high volatile bituminous in rank; maturity increases markedly in southern exposures around Radok Lake where the oldest part of the succession is exposed and some strata have been intruded by mafic dykes and ultramafic sills. The coal ash is mostly silica and aluminium oxides, indicating that the mineral ash component is mostly quartz and various clay minerals. The ratio of silica to aluminium oxides appears to increase in an upward stratigraphic direction. The coal macerals include a relatively high liptinite content (mainly sporinite) that is significantly higher than for typical Gondwana coals. Greater degrees of weathering within the floodbasin/peat mire environments associated with climatic drying towards the end of the Permian might account for both preferential sporopollenin preservation and increased silica:aluminium oxide ratios up-section. Correlation of the coal maceral components to adjacent peninsula India coals indicates the closest comparative coals of similar age and rank occur within the Godavari Basin, rather then the Mahanadi Basin, which is traditionally interpreted to have been contiguous with the Lambert Graben before Gondwanan breakup. The petrological characteristics suggest that either previous interpretations of Palaeozoic basin alignments between Antarctica and India are incorrect, or that environmental settings and post-Permian burial histories of these basins were strongly independent of their tectonic juxtaposition. A permineralized peat bed within the succession reveals that the coals predominantly comprise wood- and leaf-rich debris derived from low-diversity forest-mire communities dominated by glossopterid and noeggerathiopsid gymnosperms. ?? 2005 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗
USGS2011

Microbial community structure of hydrothermal deposits from geochemically different vent fields along the Mid-Atlantic Ridge

To evaluate the effects of local fluid geochemistry on microbial communities associated with active hydrothermal vent deposits, we examined the archaeal and bacterial communities of 12 samples collected from two very different vent fields: the basalt-hosted Lucky Strike (37°17'N, 32°16.3'W, depth 1600-1750m) and the ultramafic-hosted Rainbow (36°13'N, 33°54.1'W, depth 2270-2330m) vent fields along the Mid-Atlantic Ridge (MAR). Using multiplexed barcoded pyrosequencing of the variable region 4 (V4) of the 16S rRNA genes, we show statistically significant differences between the archaeal and bacterial communities associated with the different vent fields. Quantitative polymerase chain reaction (qPCR) assays of the functional gene diagnostic for methanogenesis ( mcr A), as well as geochemical modelling to predict pore fluid chemistries within the deposits, support the pyrosequencing observations. Collectively, these results show that the less reduced, hydrogen-poor fluids at Lucky Strike limit colonization by strict anaerobes such as methanogens, and allow for hyperthermophilic microaerophiles, like Aeropyrum . In contrast, the hydrogen-rich reducing vent fluids at the ultramafic-influenced Rainbow vent field support the prevalence of methanogens and other hydrogen-oxidizing thermophiles at this site. These results demonstrate that biogeographical patterns of hydrothermal vent microorganisms are shaped in part by large scale geological and geochemical processes.

Environmental Microbiology↗
USGS2004

Effects of Abandoned Coal-Mine Drainage on Streamflow and Water Quality in the Mahanoy Creek Basin, Schuylkill, Columbia, and Northumberland Counties, Pennsylvania, 2001

This report assesses the contaminant loading, effects to receiving streams, and possible remedial alternatives for abandoned mine drainage (AMD) within the Mahanoy Creek Basin in east-central Pennsylvania. The Mahanoy Creek Basin encompasses an area of 157 square miles (407 square kilometers) including approximately 42 square miles (109 square kilometers) underlain by the Western Middle Anthracite Field. As a result of more than 150 years of anthracite mining in the basin, ground water, surface water, and streambed sediments have been adversely affected. Leakage from streams to underground mines and elevated concentrations (above background levels) of acidity, metals, and sulfate in the AMD from flooded underground mines and (or) unreclaimed culm (waste rock) degrade the aquatic ecosystem and impair uses of the main stem of Mahanoy Creek from its headwaters to its mouth on the Susquehanna River. Various tributaries also are affected, including North Mahanoy Creek, Waste House Run, Shenandoah Creek, Zerbe Run, and two unnamed tributaries locally called Big Mine Run and Big Run. The Little Mahanoy Creek and Schwaben Creek are the only major tributaries not affected by mining. To assess the current hydrological and chemical characteristics of the AMD and its effect on receiving streams, and to identify possible remedial alternatives, the U.S. Geological Survey (USGS) began a study in 2001, in cooperation with the Pennsylvania Department of Environmental Protection and the Schuylkill Conservation District. Aquatic ecological surveys were conducted by the USGS at five stream sites during low base-flow conditions in October 2001. Twenty species of fish were identified in Schwaben Creek near Red Cross, which drains an unmined area of 22.7 square miles (58.8 square kilometers) in the lower part of the Mahanoy Creek Basin. In contrast, 14 species of fish were identified in Mahanoy Creek near its mouth at Kneass, below Schwaben Creek. The diversity and abundance of fish species in Mahanoy Creek decreased progressively upstream from 13 species at Gowen City to only 2 species each at Ashland and Girardville. White sucker (Catostomus commersoni), a pollution-tolerant species, was present at each of the surveyed reaches. The presence of fish at Girardville was unexpected because of the poor water quality and iron-encrusted streambed at this location. Generally, macroinvertebrate diversity and abundance at these sites were diminished compared to Schwaben Creek and other tributaries draining unmined basins, consistent with the observed quality of streamwater and streambed sediment. Data on the flow rate and chemistry for 35 AMD sources and 31 stream sites throughout the Mahanoy Creek Basin were collected by the USGS during high base-flow conditions in March 2001 and low base-flow conditions in August 2001. A majority of the base-flow streamwater samples met water-quality standards for pH (6.0 to 9.0); however, few samples downstream from AMD sources met criteria for acidity less than alkalinity (net alkalinity = 20 milligrams per liter as CaCO3) and concentrations of dissolved iron (0.3 milligram per liter) and total manganese (1.0 milligram per liter). Iron, aluminum, and various trace elements including cobalt, copper, lead, nickel, and zinc, were present in many streamwater samples at concentrations at which continuous exposure can not be tolerated by aquatic organisms without an unacceptable effect. Furthermore, concentrations of sulfate, iron, manganese, aluminum, and (or) beryllium in some samples exceeded drinking-water standards. Other trace elements, including antimony, arsenic, barium, cadmium, chromium, selenium, silver, and thallium, did not exceed water-quality criteria for protection of aquatic organisms or human health. Nevertheless, when considered together, concentrations of iron, manganese, arsenic, cadmium, chromium, copper, lead, nickel, and zinc in a majority of the streambed sediment samples from Mahanoy Creek and

Scientific Investigations Report↗
USGS1989

Arsenic in ground-water under oxidizing conditions, south-west United States

Concentrations of dissolved arsenic in ground-water in alluvial basins of Arizona commonly exceed 50 μg L −1 and reach values as large as 1,300 μg L −1 . Arsenic speciation analyses show that arsenic occurs in the fully oxidized state of plus 5 (As+5), most likely in the form of HAsO4 ∼2 , under existing oxidizing and pH conditions. Arsenic in source areas presumably is oxidized to soluble As before transport into the basin or, if after transport, before burial. Probable sources of arsenic are the sulphide and arsenide deposits in the mineralized areas of the mountains surrounding the basins. Arsenic content of alluvial material ranged from 2 to 88 ppm. Occurrence and removal of arsenic in ground-water are related to the pH and the redox condition of the ground-water, the oxidation state of arsenic, and sorption or exchange. Within basins, dissolved arsenic correlates (P<0.01) with dissolved molybdenum, selenium, vanadium, and fluoride and with pH, suggesting sorption of negative ions. The sorption hypothesis is further supported by enrichment of teachable arsenic in the basin-fill sediments by about tenfold relative to the crustal abundance and by as much as a thousandfold relative to concentrations found in ground-water. Silicate hydrolysis reactions, as defined within the alluvial basins, under closed conditions cause increases in pH basinward and would promote desorption. Within the region, large concentrations of arsenic are commonly associated with the central parts of basins whose chemistries evolve under closed conditions. Arsenic does not correlate with dissolved iron (r = 0.09) but may be partly controlled by iron in the solid phase. High solid-phase arsenic contents were found in red clay beds. Large concentrations of arsenic also were found in water associated with red clay beds. Basins that contain the larger concentrations are bounded primarily by basalt and andesite, suggesting that the iron content as well as the arsenic content of the basin fill may play a role in the occurrence of arsenic in ground-water. Under oxidizing conditions in Arizona, arsenic in ground-water appears to be controlled in part by sorption or desorption of HAsO4 ∼2 on active ferric oxyhydroxide surfaces.

Arizona, California, Nevada, New Mexico↗
USGS2000

Development and evaluation of consensus-based sediment quality guidelines for freshwater ecosystems

Numerical sediment quality guidelines (SQGs) for freshwater ecosystems have previously been developed using a variety of approaches. Each approach has certain advantages and limitations which influence their application in the sediment quality assessment process. In an effort to focus on the agreement among these various published SQGs, consensus-based SQGs were developed for 28 chemicals of concern in freshwater sediments ( i.e ., metals, polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and pesticides). For each contaminant of concern, two SQGs were developed from the published SQGs, including a threshold effect concentration (TEC) and a probable effect concentration (PEC). The resultant SQGs for each chemical were evaluated for reliability using matching sediment chemistry and toxicity data from field studies conducted throughout the United States. The results of this evaluation indicated that most of the TECs ( i.e ., 21 of 28) provide an accurate basis for predicting the absence of sediment toxicity. Similarly, most of the PECs ( i.e ., 16 of 28) provide an accurate basis for predicting sediment toxicity. Mean PEC quotients were calculated to evaluate the combined effects of multiple contaminants in sediment. Results of the evaluation indicate that the incidence of toxicity is highly correlated to the mean PEC quotient (R 2 = 0.98 for 347 samples). It was concluded that the consensus-based SQGs provide a reliable basis for assessing sediment quality conditions in freshwater ecosystems.

Archives of Environmental Contamination and Toxico↗
USGS1996

The composition of fluid inclusions in ore and gangue minerals from the Silesian-Cracow Mississippi Valley-type Zn-Pb deposits Poland: Genetic and environmental implications

The composition of fluids extracted from ore and gangue sulfide minerals that span most of the paragenesis of the Silesian-Cracow district was determined using a newly developed ion chromatographic (IC) technique. Ionic species determined were Na+, NH+4, Ca2+, Mg2+, K+, Rb+, Sr2+, Ba2+, Cl-, Br-, F-, I-, PO3-4, CO2-3, HS-, S2O2-3, SO2-4, NO-3, and acetate. Mineral samples included six from the Pomorzany mine and one from the Trzebionka mine which are hosted in the Triassic Muschelkalk Formation, and two samples of drill core from mineralized Upper Devonian strata. Nine paragenetically identifiable sulfide minerals occur throughout the Silesian-Cracow district. These include from earliest to latest: early iron sulfides, granular sphalerite, early galena, light-banded sphalerite, galena, dark-banded sphalerite, iron sulfides, late dark-banded sphalerite with late galena, and late iron sulfides. Seven of the minerals were sampled for fluid inclusion analysis in this study. Only the early iron sulfides and the last galena stage were not sampled. Although the number of analyses are limited to nine samples and two replicates and there is uncertainty about the characteristics of the fluid inclusions analyzed, the data show clear temporal trends in the composition of the fluids that deposited these minerals. Fluid inclusions in minerals deposited later in the paragenesis have significantly more K+, Br-, NH+4, and acetate but less Sr2+ than those deposited earlier in the paragenesis. The later minerals are also characterized by isotopically lighter sulfur and significantly more Tl and As in the solid minerals. The change in ore-fluid chemistry is interpreted to reflect a major change in the hydrologic regime of the district. Apparently, the migrational paths of ore fluids from the Upper Silesian basin changed during ore deposition and the fluids which deposited early minerals reacted with aquifers with very different geochemical characteristics than those that deposited late minerals. The early fluids may have reacted primarily with Devonian and Lower Carboniferous carbonate aquifers deeper in the basin, whereas the later fluids appear to have had extensive contact with organic-rich rocks, probably the shallower Middle and Upper Carboniferous flysch associated with coal measures. High concentrations of toxic Tl and As occur in the readily oxidized marcasite and pyrite minerals deposited by the later fluids. In general, the geochemistry of both the early and late fluids may be explained by an evaporite related origin or by water-rock modification of a saline basinal brine. When compared to the composition of fluid inclusions in Mississippi Valley-type (MVT) ore minerals from the Ozark region of the United States, fluid inclusions in minerals from Silesian-Cracow are fundamentally different, containing more Ca2+, Mg2+, NH+4, Br-, Sr2+ and acetate in all mineral stages with significantly more K+ in later stage minerals. The differences in ore fluid chemistry between the two regions are consistent with the lithologic differences of the respective basins thought to be the source of the mineralizing brines.

Prace - Panstwowego Instytutu Geologicznego↗
USGS2010

Factors Controlling Pre-Columbian and Early Historic Maize Productivity in the American Southwest, Part 1: The Southern Colorado Plateau and Rio Grande Regions

Maize is the New World's preeminent grain crop and it provided the economic basis for human culture in many regions within the Americas. To flourish, maize needs water, sunlight (heat), and nutrients (e. g., nitrogen). In this paper, climate and soil chemistry data are used to evaluate the potential for dryland (rainon-field) agriculture in the semiarid southeastern Colorado Plateau and Rio Grande regions. Processes that impact maize agriculture such as nitrogen mineralization, infiltration of precipitation, bare soil evaporation, and transpiration are discussed and evaluated. Most of the study area, excepting high-elevation regions, receives sufficient solar radiation to grow maize. The salinities of subsurface soils in the central San Juan Basin are very high and their nitrogen concentrations are very low. In addition, soils of the central San Juan Basin are characterized by pH values that exceed 8.0, which limit the availability of both nitrogen and phosphorous. In general, the San Juan Basin, including Chaco Canyon, is the least promising part of the study area in terms of dryland farming. Calculations of field life, using values of organic nitrogen for the upper 50 cm of soil in the study area, indicate that most of the study area could not support a 10-bushel/acre crop of maize. The concepts, methods, and calculations used to quantify maize productivity in this study are applicable to maize cultivation in other environmental settings across the Americas. ?? 2010 US Government.

Journal of Archaeological Method and Theory↗
USGS2008

Effectiveness of an alluvial wetland on improving ground-water quality in a municipal well field, Cedar Rapids, Iowa, 1998-2006

Nutrients and pesticides are water-quality topics of concern in Iowa. Nitrate concentrations in the Cedar River and other streams in Iowa are among the highest in the Nation. A 12-mile reach of the Cedar River upstream from Cedar Rapids, Iowa, is identified on the Total Maximum Daily Load list for nitrate impairment by the U.S. Environmental Protection Agency. In addition, pesticide concentrations in water samples from alluvial aquifers in Iowa have been ranked as some of the largest in the Nation. The Cedar River, like many rivers with alluvium, affects the alluvial aquifer that is used as a municipal water supply for Cedar Rapids, Iowa. A continuing challenge for the Cedar Rapids Water Department is to provide drinking water that meets all drinking-water regulations; this is made more of a challenge because of the high (often over 10 milligrams per liter) nitrate concentrations in the Cedar River and the presence of other potential chemicals of concern, such as pesticides. An alluvial wetland proved useful in improving water quality. Samples from observation wells completed in the alluvial wetland near the municipal well field had nitrate concentrations that were four to six times lower when compared to river or upland sites; however, iron and manganese concentrations in samples from observation wells in the wetland areas were an order of magnitude higher when compared to the river or an upgradient well. Biological and chemical reduction processes were determined to mobilize inorganic constituents in accordance with physical chemistry principles. Generally, selected pesticides and two pesticide degradates of atrazine that were sampled for in alluvial wetland wells remained relatively unchanged, and indicated only a slight decrease in concentration compared to the Cedar River water samples. Pesticides were not detected above regulatory limits in any of the observation wells; however, one sample from the Cedar River had an atrazine detection at 4.5 micrograms per liter, which is above the maximum contaminant level of 3.0 micrograms per liter for drinking-water regulations for that compound. Results indicate that alluvial wetlands may provide substantial reductions of nitrate concentrations in ground water, and may be a useful strategy for the reduction of nitrate for municipal wells. Results for reducing pesticides were less dramatic than for nitrate, as pesticide concentrations were reduced slightly from the river to the wetland.

Iowa↗
USGS1990

Rates of microbial metabolism in deep coastal plain aquifers

Rates of microbial metabolism in deep anaerobic aquifers of the Atlantic coastal plain of South Carolina were investigated by both microbiological and geochemical techniques. Rates of [2- 14 C]acetate and [U- 14 C]glucose oxidation as well as geochemical evidence indicated that metabolic rates were faster in the sandy sediments composing the aquifers than in the clayey sediments of the confining layers. In the sandy aquifer sediments, estimates of the rates of CO 2 production (millimoles of CO 2 per liter per year) based on the oxidation of [2- 14 C] acetate were 9.4 × 10 −3 to 2.4 × 10 −1 for the Black Creek aquifer, 1.1 × 10 −2 for the Middendorf aquifer, and <7 × 10 −5 for the Cape Fear aquifer. These estimates were at least 2 orders of magnitude lower than previously published estimates that were based on the accumulation of CO 2 in laboratory incubations of similar deep subsurface sediments. In contrast, geochemical modeling of groundwater chemistry changes along aquifer flowpaths gave rate estimates that ranged from 10 −4 to 10 −6 mmol of CO 2 per liter per year. The age of these sediments (ca. 80 million years) and their organic carbon content suggest that average rates of CO 2 production could have been no more than 10 −4 mmol per liter per year. Thus, laboratory incubations may greatly overestimate the in situ rates of microbial metabolism in deep subsurface environments. This has important implications for the use of laboratory incubations in attempts to estimate biorestoration capacities of deep aquifers. The rate estimates from geochemical modeling indicate that deep aquifers are among the most oligotrophic aquatic environments in which there is ongoing microbial metabolism.

South Carolina↗
USGS2008

Determination of dominant biogeochemical processes in a contaminated aquifer-wetland system using multivariate statistical analysis

Determining the processes governing aqueous biogeochemistry in a wetland hydrologically linked to an underlying contaminated aquifer is challenging due to the complex exchange between the systems and their distinct responses to changes in precipitation, recharge, and biological activities. To evaluate temporal and spatial processes in the wetland-aquifer system, water samples were collected using cm-scale multi-chambered passive diffusion samplers (peepers) to span the wetland-aquifer interface over a period of 3 yr. Samples were analyzed for major cations and anions, methane, and a suite of organic acids resulting in a large dataset of over 8000 points, which was evaluated using multivariate statistics. Principal component analysis (PCA) was chosen with the purpose of exploring the sources of variation in the dataset to expose related variables and provide insight into the biogeochemical processes that control the water chemistry of the system. Factor scores computed from PCA were mapped by date and depth. Patterns observed suggest that (i) fermentation is the process controlling the greatest variability in the dataset and it peaks in May; (ii) iron and sulfate reduction were the dominant terminal electron-accepting processes in the system and were associated with fermentation but had more complex seasonal variability than fermentation; (iii) methanogenesis was also important and associated with bacterial utilization of minerals as a source of electron acceptors (e.g., barite BaSO 4 ); and (iv) seasonal hydrological patterns (wet and dry periods) control the availability of electron acceptors through the reoxidation of reduced iron-sulfur species enhancing iron and sulfate reduction.

Journal of Environmental Quality↗
USGS2003

Geochemistry of the Birch Creek Drainage Basin, Idaho

The U.S. Survey and Idaho State University, in cooperation with the U.S. Department of Energy, are conducting studies to describe the chemical character of ground water that moves as underflow from drainage basins into the eastern Snake River Plain aquifer (ESRPA) system at and near the Idaho National Engineering and Environmental Laboratory (INEEL) and the effects of these recharge waters on the geochemistry of the ESRPA system. Each of these recharge waters has a hydrochemical character related to geochemical processes, especially water-rock interactions, that occur during migration to the ESRPA. Results of these studies will benefit ongoing and planned geochemical modeling of the ESRPA at the INEEL by providing model input on the hydrochemical character of water from each drainage basin. During 2000, water samples were collected from five wells and one surface-water site in the Birch Creek drainage basin and analyzed for selected inorganic constituents, nutrients, dissolved organic carbon, tritium, measurements of gross alpha and beta radioactivity, and stable isotopes. Four duplicate samples also were collected for quality assurance. Results, which include analyses of samples previously collected from four other sites, in the basin, show that most water from the Birch Creek drainage basin has a calcium-magnesium bicarbonate character. The Birch Creek Valley can be divided roughly into three hydrologic areas. In the northern part, ground water is forced to the surface by a basalt barrier and the sampling sites were either surface water or shallow wells. Water chemistry in this area was characterized by simple evaporation models, simple calcite-carbon dioxide models, or complex models involving carbonate and silicate minerals. The central part of the valley is filled by sedimentary material and the sampling sites were wells that are deeper than those in the northern part. Water chemistry in this area was characterized by simple calcite-dolomite-carbon dioxide models. In the southern part, ground water enters the ESRPA. In this area, the sampling sites were wells with depths and water levels much deeper than those in the northern and central parts of the valley. The calcium and carbon water chemistry in this area was characterized by a simple calcite-carbon dioxide model, but complex calcite-silicate models more accurately accounted for mass transfer in these areas. Throughout the geochemical system, calcite precipitated if it was an active phase in the models. Carbon dioxide either precipitated (outgassed) or dissolved depending on the partial pressure of carbon dioxide in water from the modeled sites. Dolomite was an active phase only in models from the central part of the system. Generally the entire geochemical system could be modeled with either evaporative models, carbonate models, or carbonate-silicate models. In both of the latter types of models, a significant amount of calcite precipitated relative to the mass transfer to and from the other active phases. The amount of calcite precipitated in the more complex models was consistent with the amount of calcite precipitated in the simpler models. This consistency suggests that, although the simpler models can predict calcium and carbon concentrations in Birch Creek Valley ground and surface water, silicate-mineral-based models are required to account for the other constituents. The amount of mass transfer to and from the silicate mineral phases was generally small compared with that in the carbonate phases. It appears that the water chemistry of well USGS 126B represents the chemistry of water recharging the ESRPA by means of underflow from the Birch Creek Valley.

Idaho↗
USGS2021

A reactive transport approach to modeling cave seepage water chemistry I: Carbon isotope transformations

The majority of Critical Zone research has emphasized silicate lithologies, which are typified by relatively slow rates of reactivity and incongruent weathering. However, the relatively simpler weathering of carbonate-dominated lithology can result in secondary mineral deposits, such as speleothems, which provide a long-term archive for Critical Zone processes. In particular, carbon isotopic variability in speleothems has the potential to provide records of changes in vegetation, soil respiration, carbon stabilization in deep soils, and/or chemical weathering in the host rock. Despite this opportunity to reconstruct many Critical Zone processes, multiple influences can also make interpretion of these speleothem carbon isotope records challenging. The integration of observational data and simulations specific to karst systems offers an interpretive framework for these unique time-averaged records accumulated through the evolution of carbonate landscapes. Here, we present a forward and process-based reactive transport simulation based on a multi-year monitoring study of Blue Spring Cave in central Tennessee, USA. The simulations describe the fluid-driven weathering of limestone including explicit tracking of dissolved calcium, stable carbon, and radiocarbon isotope ratios based on reaction rates calibrated through laboratory batch reaction data. We find that calcium concentrations and radiocarbon isotope ratios are strongly influenced by the combination of fluid flow rate and soil CO 2 content, and require rapid gas phase communication between the overlying soil boundary condition and interior karst to sustain both elevated limestone weathering rates and relatively modern radiocarbon signatures. Stable carbon isotopes are largely dictated by temperature-dependent equilibrium fractionation among contemporaneous species. These simulations are extended to a wide range of parameter space to demonstrate the environmental factors that these isotope proxies record.

Geochimica et Cosmochimica Acta↗
USGS2014

Groundwater quality at Alabama Plating and Vincent Spring, Vincent, Alabama, 2007–2008

The former Alabama Plating site in Vincent, Alabama, includes the location where the Alabama Plating Company operated an electroplating facility from 1956 until 1986. The operation of the facility generated waste containing cyanide, arsenic, cadmium, chromium, copper, lead, zinc, and other heavy metals. Contamination resulting from the site operations was identified in groundwater, soil, and sediment. Vincent Spring, used as a public water supply by the city of Vincent, Alabama, is located about ½ mile southwest of the site. The U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, conducted an investigation at Vincent Spring and the Alabama Plating site, Vincent, Alabama, during 2007–2008 to evaluate the groundwater quality and evaluate the potential effect of contaminated groundwater on the water quality of Vincent Spring. The results of the investigation will provide scientific data and information on the occurrence, fate, and transport of contaminants in the water resources of the area and aid in the evaluation of the vulnerability of the public water supply to contamination. Samples were analyzed to evaluate the water quality at the former plating site, investigate the presence of possible contaminant indicators at Vincent Spring, and determine the usefulness of stable isotopes and geochemical properties in understanding groundwater flow and contaminant transport in the area. Samples collected from 16 monitor wells near the plating site and Vincent Spring were analyzed for major constituents, trace metals, nutrients, and the stable isotopes for hydrogen ( 2 H/H) and oxygen ( 18 O/ 16 O). Groundwater collected from Vincent Spring was characterized as a calcium-magnesium-bicarbonate water type with total dissolved solids concentrations ranging from 110 to 120 milligrams per liter and pH ranging from about 7.5 to 7.9 units. Groundwater chemistry at the monitor wells at the Alabama Plating site was highly variable by location and depth. Dissolved solids concentrations ranged from 28 to 2,880 milligrams per liter, and the water types varied from calcium-magnesium-bicarbonate-chloride, to calcium-sulfate or calcium-magnesium-sulfate, to sodium-chloride water types. The stable isotope ratios for hydrogen ( 2 H/H) and oxygen ( 18 O/ 16 O) for water from the monitor wells and from Vincent Spring, based on a single sampling event, can be separated into three groups: (1) Vincent Spring, (2) monitor wells MW03 and MW28, and (3) the remaining Alabama Plating monitor wells. The geochemical and stable isotope analyses indicate that water from Vincent Spring is distinct from water from the Alabama Plating monitor wells; however, this evaluation is based on a single sampling event. Although the water from Vincent Spring, for this sampling event, is different and does not seem to be affected by contaminated groundwater from the Alabama Plating site, additional hydrologic and water-quality data are needed to fully identify flow paths, the potential for contaminant transport, and water-quality changes through time.

Alabama↗
USGS2014

Small reservoir distribution, rate of construction, and uses in the upper and middle Chattahoochee basins of the Georgia Piedmont, USA, 1950-2010

Construction of small reservoirs affects ecosystem processes in numerous ways including fragmenting stream habitat, altering hydrology, and modifying water chemistry. While the upper and middle Chattahoochee River basins within the Southeastern United States Piedmont contain few natural lakes, they have a high density of small reservoirs (more than 7500 small reservoirs in the nearly 12,000 km2 basin). Policymakers and water managers in the region have little information about small reservoir distribution, uses, or the cumulative inundation of land cover caused by small reservoir construction. Examination of aerial photography reveals the spatiotemporal patterns and extent of small reservoir construction from 1950 to 2010. Over that 60 year timeframe, the area inundated by water increased nearly six fold (from 19 reservoirs covering 0.16% of the study area in 1950 to 329 reservoirs covering 0.95% of the study area in 2010). While agricultural practices were associated with reservoir creation from 1950 to 1970, the highest rates of reservoir construction occurred during subsequent suburban development between 1980 and 1990. Land cover adjacent to individual reservoirs transitioned over time through agricultural abandonment, land reforestation, and conversion to development during suburban expansion. The prolific rate of ongoing small reservoir creation, particularly in newly urbanizing regions and developing counties, necessitates additional attention from watershed managers and continued scientific research into cumulative environmental impacts at the watershed scale.

Georgia↗
USGS2025

Quality of groundwater used for domestic supply in the Gilroy-Hollister basin and surrounding areas, California, 2022

More than 2 million Californians rely on groundwater from domestic wells for drinking-water supply. This report summarizes a 2022 California Groundwater Ambient Monitoring and Assessment Priority Basin Project (GAMA-PBP) water-quality survey of 33 domestic and small-system drinking-water supply wells in the Gilroy-Hollister Valley groundwater basin and the surrounding areas, where more than 20,000 residents are estimated to utilize privately owned domestic wells. The study area includes the Llagas subbasin in the north, the North San Benito subbasin in the south, and the surrounding uplands. The study was focused on groundwater resources used for domestic drinking-water supply, which are mostly drawn from shallower parts of aquifer systems rather than those of groundwater resources used for public drinking-water supply in the same area. This assessment characterized the quality of ambient groundwater in the aquifer before filtration or treatment, rather than the quality of drinking water delivered to the tap. To provide context, the measured concentrations of constituents in groundwater were compared to Federal and California State regulatory and non-regulatory benchmarks for drinking-water quality. A grid-based method was used to estimate the areal proportions of groundwater resources used for domestic drinking wells that have water-quality constituents present at high concentrations (above the benchmark), moderate concentrations (between one-half of the benchmark and the benchmark for inorganic constituents, or between one-tenth of the benchmark and the benchmark for organic constituents), and low concentrations (less than one-half or one-tenth the benchmark for inorganic and organic constituents, respectively). This method provides statistically representative results at the study-area scale and permits comparisons to other GAMA-PBP study areas. In the study area, inorganic constituents in groundwater were greater than regulatory benchmarks (U.S. Environmental Protection Agency [EPA] or State of California maximum contaminant levels [MCLs]) for public drinking-water quality in 24 percent of domestic groundwater resources. The inorganic constituents present at concentrations greater than MCLs for drinking water were nitrate (as nitrogen), barium, chromium, and selenium. Total dissolved solids (TDS) or manganese were present at concentrations greater than the secondary maximum contaminant levels (SMCLs) that the State of California uses as aesthetic-based benchmarks in 48 percent of domestic groundwater resources. No volatile organic compounds or pesticide constituents were present at concentrations greater than regulatory benchmarks. Total coliform bacteria and enterococci were detected in 4 percent of domestic groundwater resources. Per- and polyfluoroalkyl substances (PFAS) were detected in 19 percent of domestic groundwater resources, and 10 percent had concentrations greater than recently enacted (April 2024) EPA MCLs. Physical and chemical factors from natural and anthropogenic sources that could affect the groundwater quality were evaluated using results from statistical testing of associations between constituent concentrations and potential explanatory variables. In this study, relevant physical factors include well construction characteristics, groundwater age, site proximity to groundwater recharge or discharge zones, and potential sources of contamination. Relevant chemical factors include the initial chemistry of the recharge water, the mineralogy of the aquifer sediments, and the subsequent shifts in chemistry as biologic and geologic reactions alter groundwater in the subsurface. Nitrate concentrations were correlated to agricultural land use, distance from the boundary of the Gilroy-Hollister Valley groundwater basin, and the proportion of modern (post-1950s) water captured by the well. Denitrification under anoxic redox conditions can mitigate some nitrate derived from fertilizer application. Total dissolved solids primarily were derived from water-rock interactions with soils and aquifer materials in the study area, but there were high concentrations where agricultural practices contributed additional TDS. Mineralogy of aquifer sediments and rocks also affect barium, selenium, boron, and chromium concentrations in the Gilroy-Hollister Valley groundwater basin. PFAS were positively correlated with urban land use and the proportion of modern water captured by the well.

California↗
USGS2005

Climate dependency of tree growth suppressed by acid deposition effects on soils in Northwest Russia

Increased tree growth in temperate and boreal forests has been proposed as a direct consequence of a warming climate. Acid deposition effects on nutrient availability may influence the climate dependency of tree growth, however. This study presents an analysis of archived soil samples that has enabled changes in soil chemistry to be tracked with patterns of tree growth through the 20th century. Soil samples collected in 1926, 1964, and 2001, near St. Petersburg, Russia, showed that acid deposition was likely to have decreased root-available concentrations of Ca (an essential element) and increased root-available concentrations of Al (an inhibitor of Ca uptake). These soil changes coincided with decreased diameter growth and a suppression of climate-tree growth relationships in Norway spruce. Expected increases in tree growth from climate warming may be limited by decreased soil fertility in regions of northern and eastern Europe, and eastern North America, where Ca availability has been reduced by acidic deposition. ?? 2005 American Chemical Society.

Environmental Science & Technology↗
USGS1997

Mercury accumulation in Devils Lake, North Dakota effects of environmental variation in closed-basin lakes on mercury chronologies

Sediment cores were collected from lakes in the Devils Lake Basin in North Dakota to determine if mercury (Hg) accumulation chronologies from sediment-core data are good indicators of variations in Hg accumulation rates in saline lakes. Sediment cores from Creel Bay and Main Bay, Devils Lake were selected for detailed analysis and interpretation. The maximum Hg concentration in the Creel Bay core was 0.15 micrograms per gram at 8 to 9 centimeters. The maximum Hg concentration in the Main Bay core was 0.07 micrograms per gram at 5 to 7 centimeters. The general decreases in Hg concentrations with depth are attributed to historic variations in atmospheric Hg deposition rate. Hg stratigraphies combined with 210Pb and 137Cs dating analyses yield Hg chronologies that indicate a general increase in Hg accumulation rates in Devils Lake since the middle of the 19th century. Mean modern Hg accumulation rates in Creel Bay were 4.9 nanograms per square centimeter per year, and rates in Main Bay were 1.8 nanograms per square centimeter per year. Mean preindustrial Hg accumulation rates in Creel Bay were 1.2 nanograms per square centimeter per year, and rates in Main Bay were 1.6 nanograms per square centimeter per year. Relatively low Hg concentrations in recent sediments in the Devils Lake Basin, along with similarities in Hg accumulation rates between lakes in the Devils Lake Basin and other lakes in the northern interior of North America, indicate that local sources of Hg are not important sources of Hg. Results of the study indicate that accurate Hg chronologies are discernible in sediment cores collected from saline lakes. However, spatial and temporal variations in lake level and water chemistry common to saline lakes make interpretation of radioisotopic and geochemical chronologies difficult. Hg geochemistry in Devils Lake, and presumably in other saline lakes, is dynamic. The results of this study indicate that the absolute amount of sediment transported to Devils Lake, along with the associated Hg and total organic carbon, and the distribution of sedimentation patterns in Devils Lake may be affected by changing lake levels.

Water, Air, & Soil Pollution↗
USGS2021

Robust projections of future fire probability for the conterminous United States

Globally increasing wildfires have been attributed to anthropogenic climate change. However, providing decision makers with a clear understanding of how future planetary warming could affect fire regimes is complicated by confounding land use factors that influence wildfire and by uncertainty associated with model simulations of climate change. We use an ensemble of statistically downscaled Global Climate Models in combination with the Physical Chemistry Fire Frequency Model (PC2FM) to project changing potential fire probabilities in the conterminous United States for two scenarios representing lower (RCP 4.5) and higher (RCP 8.5) greenhouse gas emission futures. PC2FM is a physically-based and scale-independent model that predicts mean fire return intervals from both fire reactant and reaction variables, which are largely dependent on a locale's climate. Our results overwhelmingly depict increasing potential fire probabilities across the conterminous US for both climate scenarios. The primary mechanism for the projected increases is rising temperatures, reflecting changes in the chemical reaction environment commensurate with enhanced photosynthetic rates and available thermal molecular energy. Existing high risk areas, such as the Cascade Range and the Coastal California Mountains, are projected to experience greater annual fire occurrence probabilities, with relative increases of 122% and 67%, respectively, under RCP 8.5 compared to increases of 63% and 38% under RCP 4.5. Regions not currently associated with frequently occurring wildfires, such as New England and the Great Lakes, are projected to experience a doubling of occurrence probabilities by 2100 under RCP 8.5. This high resolution, continental-scale modeling study of climate change impacts on potential fire probability accounts for shifting background environmental conditions across regions that will interact with topographic drivers to significantly alter future fire probabilities. The ensemble modeling approach presents a useful planning tool for mitigation and adaptation strategies in regions of increasing wildfire risk.

Science of the Total Environment↗