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At least 1,009 records · Page 56Linked to original sources
USGS2012

The Spar Lake strata-Bound Cu-Ag deposit formed across a mixing zone between trapped natural gas and metals-bearing brine

Ore formation at the Spar Lake red bed-associated strata-bound Cu deposit took place across a mixing and reaction zone between a hot oxidized metals-transporting brine and a reservoir of “sour” (H 2 S-bearing) natural gas trapped in the host sandstones. Fluid inclusion volatile analyses have very high CH 4 concentrations (≥1 mol % in most samples), and a sample from the fringe of the deposit has between 18 and 36 mol % CH 4 . The ratio of CH 4 /CO 2 in fluid inclusions appears to vary regularly across the deposit, with the lowest CH 4 /CO 2 ratios from high-grade chalcocite-bearing ore, and the highest from the chalcopyrite-bearing fringe. The helium R/R a isotope ratios (0.23–0.98) and concentrations define a mixture between crustal and atmospheric helium. The volatiles in fluid inclusions (CH 4 , CO 2 , H 2 S, SO 2 , H 2 , H 2 O, and other organic gases) and values of f O 2 and temperature calculated from the volatiles data all show gradations across the deposit that are completely consistent with such a mixing and reaction zone. Other volatiles from the fluid inclusions (HCl, HF, 3 He, Msup>4 He, N 2 , Ar) characterize the brine and give evidence for only shallow crustal fluids with no magmatic influences. The brine entered the gas reservoir from below and along the axis of the deposit and migrated out along bedding to the southwest, northeast, and northwest. Metals-transporting brines may have been fed into the host sandstones from the East Fault, but that remains uncertain. Abundant ore-stage Fe and Mn calcite cements from the reduced fringe have δ 13 C values as low as −18.4‰, and many values less than −10‰, which indicate that significant carbonate was generated by oxidation of organic carbon from the natural gas. The zone of calcite cements with very low δ 13 C values approximately envelopes chalcocite-bearing ore. Sulfur isotope data of Cu, Pb, and Fe sulfides and barite indicate derivation of roughly half of the orebody sulfide directly from sour gas H 2 S. That sour gas H 2 S had developed in steps known from other sedimentary basins, starting with (1) bacterial sulfate reduction (BSR) of seawater sulfate having δ 34 S of about 20‰ and sequestering of the sulfide in organic matter in source rocks stratigraphically below the deposit host rocks, followed by (2) maturation of the sulfide-bearing organic matter into liquid petroleum with relatively homogeneous sulfide having δ 34 S of 5 ± 5‰, then by (3) thermal cracking of the oil to CH 4 and H 2 S with relatively homogeneous sulfide having δ 34 S closely distributed, about 6‰. The CH 4 and H 2 S migrated and were trapped in sandstones of the upper member of the Revett Formation, where they were later met by the 200°C metals-transporting brine. There was additional contribution of sulfide to ore from later thermochemical sulfate reduction (TSR) operating on sulfate δ 34 S of 20 to 29‰ in both formation waters and metals-transporting solutions. A large range of δ 34 S in sulfides resulted as the 6‰ sour gas sulfide was supplemented with varying proportions of 20 to 29‰ sulfide from TSR.

Economic Geology↗
USGS1957

Some limitations on the possible composition of the ore-forming fluid

The activity ratios of various important anions (S (super =) , CO 3 (super =) , SO 4 (super =) , OH (super -) , F (super -) , and Cl (super -) ) in hydrothermal solutions at the time of deposition are evaluated using a simple thermodynamic technique. The ratios are interpreted in the light of the mineralogy of ore deposits and limits are placed on the variability of each ratio in hydrothermal solutions. All of the calculations are made for 25 degrees C and cautious extrapolation to higher temperatures seems justified; however, additional data for elevated temperatures and pressures are needed before more than approximate values may be assigned to these ratios in the ore-forming fluid.The calculated partial pressure of CO 2 in the ore fluid is generally less than one atmosphere, which suggests that a dense CO 2 phase cannot be considered an important ore fluid for most deposits. The partial pressure of H 2 S is usually less than 10 (super -4) atmosphere, which makes it extremely difficult to defend the theory that metals (other than the easily complexible mercury, arsenic, antimony, and perhaps gold and silver) are transported in quantity as complex sulfides or hydrosulfides. The sulfate to sulfide ratio is such that the oxidation potential at the time of deposition is defined by the following equation: Eh (in volts) = 0.22 + or - 0.04 - 0.059 pH.

Economic Geology↗
USGS2000

Calcium depletion in a Southeastern United States forest ecosystem

Forest soil Ca depletion through leaching and vegetation uptake may threaten long-term sustainability of forest productivity in the southeastern USA. This study was conducted to assess Ca pools and fluxes in a representative southern Piedmont forest to determine the soil Ca depletion rate. Soil Ca storage, Ca inputs in atmospheric deposition, and outputs in soil leaching and vegetation uptake were investigated at the Panola Mountain Research Watershed (PMRW) near Atlanta, GA. Average annual outputs of 12.3 kg ha −1 yr −1 in uptake into merchantable wood and 2.71 kg ha −1 yr −1 soil leaching exceeded inputs in atmospheric deposition of 2.24 kg ha −1 yr −1 The annual rate of Ca uptake into merchantable wood exceeds soil leaching losses by a factor of more than five. The potential for primary mineral weathering to provide a substantial amount of Ca inputs is low. Estimates of Ca replenishment through mineral weathering in the surface 1 m of soil and saprolite was estimated to be 0.12 kg ha −1 yr −1 The weathering rate in saprolite and partially weathered bedrock below the surface 1 m is similarly quite low because mineral Ca is largely depleted. The soil Ca depletion rate at PMRW is estimated to be 12.7 kg ha −1 yr −1 At PMRW and similar hardwood-dominated forests in the Piedmont physiographic province, Ca depletion will probably reduce soil reserves to less than the requirement for a merchantable forest stand in ≈80 yr. This assessment and comparable analyses at other southeastern USA forest sites suggests that there is a strong potential for a regional problem in forest nutrition in the long term.

Soil Science Society of America Journal↗
USGS2003

Formation and loss of humic substances during decomposition in a pine forest floor

Since twice as much C is sequestered in soils as is contained in the atmosphere, the factors controlling the decomposition rate of soil C are important to the assessment of the effects of climatic change. The formation of chemically resistant humic substances might be an important process controlling recycling of CO 2 to the atmosphere. Our objectives were to measure the rate of formation and loss of humic substances during 13 yr of litter decomposition . We placed nets on the floor of a white pine (Pinus strobus) forest to separate each annual layer of litter for 13 yr and measured humic substance concentration using NaOH extraction followed by chromatographic fractionation. The humic acid fraction increased from 2.1% of the C in litterfall to 15.7% after 1 yr. On a grams per square meter (g m -2 ) basis the humic substance fraction increased during the first year and then declined, with a half decay time (t 1/2 ) of 5.1 yr, which was significantly slower than the bulk litter (t 1/2 = 3.9 yr). The carboxylic C concentration estimated from 13 C nuclear magnetic resonance (NMR) increased in the litter over time, though total mass of carboxylic acid C in the forest floor also declined over the 13-yr period (t 1/2 = 4.6 yr). While humic substances in the forest floor decomposed at a somewhat slower rate than bulk litter during Years 1 to 13, they decomposed much faster than has been calculated from 14 C dating of the refractory fraction of organic matter in the mineral soil.

Soil Science Society of America Journal↗
USGS2016

Experimental studies and model analysis of noble gas fractionation in porous media

The noble gases, which are chemically inert under normal terrestrial conditions but vary systematically across a wide range of atomic mass and diffusivity, offer a multicomponent approach to investigating gas dynamics in unsaturated soil horizons, including transfer of gas between saturated zones, unsaturated zones, and the atmosphere. To evaluate the degree to which fractionation of noble gases in the presence of an advective–diffusive flux agrees with existing theory, a simple laboratory sand column experiment was conducted. Pure CO2 was injected at the base of the column, providing a series of constant CO2 fluxes through the column. At five fixed sampling depths within the system, samples were collected for CO2 and noble gas analyses, and ambient pressures were measured. Both the advection–diffusion and dusty gas models were used to simulate the behavior of CO2 and noble gases under the experimental conditions, and the simulations were compared with the measured depth-dependent concentration profiles of the gases. Given the relatively high permeability of the sand column (5 ´ 10−11 m2), Knudsen diffusion terms were small, and both the dusty gas model and the advection–diffusion model accurately predicted the concentration profiles of the CO2 and atmospheric noble gases across a range of CO2 flux from ?700 to 10,000 g m−2 d−1. The agreement between predicted and measured gas concentrations demonstrated that, when applied to natural systems, the multi-component capability provided by the noble gases can be exploited to constrain component and total gas fluxes of non-conserved (CO2) and conserved (noble gas) species or attributes of the soil column relevant to gas transport, such as porosity, tortuosity, and gas saturation.

Vadose Zone Journal↗
USGS1991

Global warming and prairie wetlands: potential consequences for waterfowl habitat

The accumulation of greenhouse gasses in the atmosphere is expected to warm the earth's climate at an unprecedented rate (Ramanathan 1988, Schneider 1989). If the climate models are correct, within 100 years the earth will not only be warmer than it has been during the past million years, but the change will have occurred more rapidly than any on record. Many profound changes in the earth's environment are expected, including rising sea level, increasing aridity in continental interiors, and melting permafrost. Ecosystems are expected to respond variously to a rapidly changing climate. Tree ranges in eastern North American are expected to shift northward, and seed dispersal may not be adequate to maintain current diversity (Cohn 1989, Johnson and Webb 1989). In coastal wetlands, rising sea level from melting icecaps and thermal expansion could flood salt-grass marshes and generally reduce the size and productivity of the intertidal zone (Peters and Darling 1985). As yet, little attention has been given to the possible effects of climatic warming on inland prairie wetland ecosystems. These wetlands, located in the glaciated portion of the North American Great Plains (Figure 1), constitute the single most important breeding area for waterfowl on this continent (Hubbard 1988). This region annually produces 50-80% of the continent's total duck production (Batt et al. 1989). These marshes also support a variety of other wildlife, including many species of nongame birds, muskrat, and mink (Kantrud et al. 1989a). Prairie wetlands are relatively shallow, water-holding depressions that vary in size, water permanence, and water chemistry. Permanence types include temporary ponds (typically holding water for a few weeks in the springs), seasonal ponds (holding water from spring until early summer), semipermanent ponds (holding water throughout the growing season during most years), and large permanent lakes (Stewart and Kantrud 1971). Refilling usually occurs in spring from precipitation and runoff from melting snow on frozen or saturated soils (Figure 2). Annual water levels fluctuate widely due to climate variability in the Great Plains (Borchert 1950, Kantrud et al. 1989b). Climate affects the quality of habitat for breeding waterfowl by controlling regional water conditions--water depth, areal extent, and length of wet/dry cycles (Cowardin et al. 1988)--and vegetation patterns such as the cover ration (the ratio of emergent plant cover to open water). With increased levels of atmospheric carbon dioxide, climate models project warmer and, in some cases, drier conditions for the northern Great Plains (Karl et al. 1991, Manabe and Wetherald 1986, Mitchell 1983, Rind and Lebedeff 1984). In general, a warmer, drier climate could lower waterfowl production directly by increasing the frequency of dry basins and indirectly by producing less favorable cover rations (i.e., heavy emergent cover with few or no open-water areas). The possibility of diminished waterfowl production in a greenhouse climate comes at a time when waterfowl numbers have sharply declined for other reasons (Johnson and Shaffer 1987). Breeding habitat continues to be lost or altered by agriculture, grazing, burning, mowing, sedimentation, and drainage (Kantrud et al. 1989b). For example, it has been estimated that 60% of the wetland area in North Dakota has been drained (Tiner 1984). Pesticides entering wetlands from adjacent agricultural fields have been destructive to aquatic invertebrate populations and have significantly lowered duckling survival (Grue et al. 1988). In this article, we discuss current understanding and projections of global warming; review wetland vegetation dynamics to establish the strong relationship among climate, wetland hydrology, vegetation patterns, and waterflow habitat; discuss the potential effects of a greenhouse warming on these relationships; and illustrate the potential effects of climate change on wetland habitat by using a simulation model. The extent to which intensive management of the waterfowl resource will be needed in the future strongly depends on whether a changing climate exacerbates the current problem of waterfowl decline. Should this occur, efforts outlined the recent North American Waterfowl Management Plan between the United States and Canada to reduce the current decline (Patterson and Nelson 1988) may need to be redoubled in coming years.

BioScience↗
USGS2023

Early Pliocene (Zanclean) stratigraphic framework for PRISM5/PlioMIP3 time slices

Global reconstructions of Pliocene climate provide important insights into how the climate system operates under elevated temperatures and atmospheric CO2 levels. These reconstructions have been used extensively in paleoclimate modeling experiments for comparison to simulated conditions, and as boundary conditions.Most previous work focused on the Late Pliocene interval known as the mid Piacenzian Warm Period (mPWP), the interval originally identified by the U.S. Geological Survey Pliocene Research, Interpretation and Synoptic Mapping Project (PRISM) as the PRISM interval or Mid Pliocene Warm Period. The term Mid Pliocene Warm Period is a misnomer due to changes to the geological time scale, and its use should be discontinued. The Pliocene Model Intercomparison Project (PlioMIP), now in its third phase, is expanding to include a focus on the Early Pliocene (Zanclean). PlioMIP3 experiments will allow comparison of environmental and climatic conditions before and after closure of the Central American Seaway (CAS). PlioMIP3 used the annual insolation pattern at the top of the atmosphere to determine time slices in the Zanclean that have orbital configurations that are most similar to modern. Two have been selected by PlioMIP and adopted by PRISM for inclusion in future studies: PRISM5.1 (4.474 Ma) and PRISM5.2 (4.870 Ma). Here we establish the stratigraphic framework for these Early Pliocene time slices and furnish information to help locate these intervals in proxy records of paleoenvironmental data using oxygen isotope stratigraphy, paleomagnetic stratigraphy, biostratigraphy, and biochronology (calibrated planktic foraminifer and calcareous nannofossil events).

Stratigraphy↗
USGS2026

Effects of external water on volcanic column height and collapse

Volcanic plumes are important because they spread volcanic material, can impact climate, and pose hazards to aviation. Among eruption processes, column collapse is arguably the most consequential in terms of direct impacts, as it marks the onset of ground-hugging pyroclastic density currents that pose the greatest immediate threat to life and infrastructure. This study inves- tigates how external water, such as is incorporated during subaqueous eruptions, affects the critical condition (including mass eruption rate, temperature, and gas fraction) at which column collapse occurs in the atmosphere, referred to as “the column collapse condition”. We use the 1-D plume model, Plumeria , to explore how variations in external water (0–60 wt.%), vent exit velocity (75–125 m s −1 ), and initial magma temperature (700–1100 °C) affect the column collapse condition. We find that the occurrence of column collapse is highly sensitive to the amount of external water. Small amounts of external water (⪅ 25 wt.%) suppress column collapse, whereas higher amounts of water encourage collapse. Using more than 150,000 simulations, we map out the highly non-linear shape of the column collapse condition as a function of mass eruption rates and external water contents. The Richardson number, the ratio of buoyancy to shear forces, offers a useful framework for defining the column collapse condition for eruptions involving external water. This work enhances our understanding of how external water ingestion affects volcanic plume dynamics, including height and column collapse conditions. Recent shallow submarine eruptions that produced very tall atmospheric plumes and partial column collapse (e.g. the 2021 Fukutoku-Oka-no-Ba eruption in Japan and the 2022 Hunga eruption in Tonga) demonstrate the importance of understanding how external water influences the collapse of eruption columns.

Volcanica↗
USGS2023

Biophysical warming patterns of an open-top chamber and its short-term influence on a Phragmites wetland ecosystem in China

Passive-warming, open-top chambers (OTCs) are widely applied for studying the effects of future climate warming on coastal wetlands. In this study, a set of six OTCs were established at a Phragmites wetland located in the Yellow River Delta of Dongying City, China. With data collected through online transmission and in-situ sensors, the attributes and patterns of realized OTCs warming are demonstrated. The authors also quantified the preliminary influence of experimental chamber warming on plant traits. OTCs produced an elevated average air temperature of 0.8°C (relative to controls) during the growing season (June to October) of 2018, and soil temperatures actually decreased by 0.54°C at a depth of 5 cm and 0.46°C at a depth of 30 cm in the OTCs. Variations in diel patterns of warming depend greatly on the heat sources of incoming radiation in the daytime versus soil heat flux at night. Warming effects were often larger during instantaneous analyses and influenced OTCs air temperatures from −2.5°C to 8.3°C dependent on various meteorological conditions at any given time, ranging from cooling influences from vertical heat exchange and vegetation to radiation-associated warming. Night-time temperature depressions in the OTCs were due to the low turbulence inside OTCs and changes in surface soil-atmosphere heat transfer. Plant shoot density, basal diameter, and biomass of Phragmites decreased by 23.2%, 6.3%, and 34.0%, respectively, under experimental warming versus controls, and plant height increased by 4.3%, reflecting less carbon allocation to stem structures as plants in the OTCs experienced simultaneous wind buffering. While these passive-warming OTCs created the desired warming effects both to the atmosphere and soils, pest damages on the plant leaves and lodging within the OTCs were extensive and serious, creating the need to consider control options for these chambers and the replicated OTCs studies underway in other Chinese Phragmites marshes (Panjin and Yancheng).

Shandong Province↗
USGS2003

Geothermal energy: clean power from the Earth's heat

Societies in the 21st century require enormous amounts of energy to drive the machines of commerce and to sustain the lifestyles that many people have come to expect. Today, most of this energy is derived from oil, natural gas, and coal, supplemented by nuclear power. Local exceptions exist, but oil is by far the most common source of energy worldwide. Oil resources, however, are nonrenewable and concentrated in only a few places around the globe, creating uncertainty in long-term supply for many nations. At the time of the Middle East oil embargo of the 1970s, about a third of the United States oil supply was imported, mostly from that region. An interruption in the flow of this import disrupted nearly every citizen’s daily life, as well as the Nation’s economy. In response, the Federal Government launched substantial programs to accelerate development of means to increasingly harness “alternative energies”—primarily biomass, geothermal, solar, and wind. The new emphasis on simultaneously pursuing development of several sources of energy recognized the timeless wisdom found in the proverb of “not putting all eggs in one basket.” This book helps explain the role that geothermal resources can play in helping promote such diversity and in satisfying our Nation’s vast energy needs as we enter a new millennium. For centuries, people have enjoyed the benefits of geothermal energy available at hot springs, but it is only through technological advances made during the 20th century that we can tap this energy source in the subsurface and use it in a variety of ways, including the generation of electricity. Geothermal resources are simply exploitable concentrations of the Earth’s natural heat (thermal energy). The Earth is a bountiful source of thermal energy, continuously producing heat at depth, primarily by the decay of naturally occurring radioactive isotopes—principally of uranium, thorium, and potassium—that occur in small amounts in all rocks. This heat then rises to and through the Earth’s surface, where it escapes into the atmosphere. The amount of heat that flows annually from the Earth into the atmosphere is enormous—equivalent to ten times the annual energy consumption of the United States and more than that needed to power all nations of the world, if it could be fully harnessed. Even if only 1 percent of the thermal energy contained within the uppermost 10 kilometers of our planet could be tapped, this amount would be 500 times that contained in all oil and gas resources of the world. How might we benefit from this vast amount of thermal energy beneath our feet? Where, by what means, and how much of the Earth’s natural heat can be usefully harnessed? These are especially important questions to contemplate, because global population is expected to soon exceed seven billion and many scientists believe that the world’s fossilfuel resources may be substantially depleted within this century. Faced with such prospects, both the public and private sectors are working toward more fully utilizing the Earth’s abundant thermal energy and other alternative energy resources. A skeptic might question the wisdom of devoting much national effort to geothermal energy development, especially because many experts think that geothermal heat can contribute at most about 10 percent to the Nation’s energy supply using current technologies. However, ongoing advances in exploration and heat-extraction technologies are improving our ability to use the resource and may substantially increase the geothermal contribution to the Nation’s energy supply. In an attempt to help national planners and average citizens alike understand the nature and energy potential of geothermal resources, this book (1) describes the distribution and nature of geothermal energy, (2) reviews the common types of geothermal systems that provide useful energy with current technology, (3) considers potential geothermal resources that might someday be tapped with developing technologies, and (4) summarizes the role of earth-science information in assessing and harnessing geothermal resources wherever they occur worldwide. The predecessor to this book (Tapping the Earth’s Natural Heat, U.S. Geological Survey Circular 1125, published in 1994) summarized the situation in the early 1990s. In an effort to support national energy planners, this new circular incorporates more recent advances in geothermal science and technology.

Circular↗
USGS2007

Water Budgets: Foundations for Effective Water-Resources and Environmental Management

INTRODUCTION Water budgets provide a means for evaluating availability and sustainability of a water supply. A water budget simply states that the rate of change in water stored in an area, such as a watershed, is balanced by the rate at which water flows into and out of the area. An understanding of water budgets and underlying hydrologic processes provides a foundation for effective water-resource and environmental planning and management. Observed changes in water budgets of an area over time can be used to assess the effects of climate variability and human activities on water resources. Comparison of water budgets from different areas allows the effects of factors such as geology, soils, vegetation, and land use on the hydrologic cycle to be quantified. Human activities affect the natural hydrologic cycle in many ways. Modifications of the land to accommodate agriculture, such as installation of drainage and irrigation systems, alter infiltration, runoff, evaporation, and plant transpiration rates. Buildings, roads, and parking lots in urban areas tend to increase runoff and decrease infiltration. Dams reduce flooding in many areas. Water budgets provide a basis for assessing how a natural or human-induced change in one part of the hydrologic cycle may affect other aspects of the cycle. This report provides an overview and qualitative description of water budgets as foundations for effective water-resources and environmental management of freshwater hydrologic systems. Perhaps of most interest to the hydrologic community, the concepts presented are also relevant to the fields of agriculture, atmospheric studies, meteorology, climatology, ecology, limnology, mining, water supply, flood control, reservoir management, wetland studies, pollution control, and other areas of science, society, and industry. The first part of the report describes water storage and movement in the atmosphere, on land surface, and in the subsurface, as well as water exchange among these compartments. Our ability to measure these phenomena and inherent uncertainties in measurement techniques also are discussed. The latter part of the report presents a number of case studies that illustrate how water-budget studies are conducted, documents how human activities affect water budgets, and describes how water budgets are used to address water and environmental issues.

Circular↗
USGS1984

Acid precipitation; an annotated bibliography

This collection of 1660 bibliographies references on the causes and environmental effects of acidic atmospheric deposition was compiled from computerized literature searches of earth-science and chemistry data bases. Categories of information are (1) atmospheric chemistry (gases and aerosols), (2) precipitation chemistry, (3) transport and deposition (wet and dry), (4) aquatic environments (biological and hydrological), (5) terrestrial environments, (6) effects on materials and structures, (7) air and precipitation monitoring and data collection, and (8) modeling studies. References date from the late 1800 's through December 1981. The bibliography includes short summaries of most documents. Omitted are unpublished manuscripts, publications in press, master 's theses and doctoral dissertations, newspaper articles, and book reviews. Coauthors and subject indexes are included. (USGS)

Circular↗
USGS2014

A 19-year record of chemical and isotopic composition of water from springs of the Shenandoah National Park, Virginia, 1995-2014

During October 1995 through March 2014, the U.S. Geological Survey in cooperation with the National Park Service, Luray, Virginia Station collected and analyzed samples of selected springs, air and unsaturated-zone gases in Shenandoah National Park, Virginia. The 19-year record of measurements of chemical and isotopic composition of water discharging from 34 springs located along the crest of the Blue Ridge Mountains in Shenandoah National Park, Virginia, is reported. These data include field measurements of water temperature, specific conductance, concentrations of dissolved oxygen (O 2 ), and pH. Laboratory measurements included major-, minor-, and trace-element chemistry; concentrations of dissolved gases (nitrogen, [N 2 ] argon [Ar], oxygen, and carbon dioxide [CO 2 ]); concentrations of dissolved trace atmospheric gases, including trichlorofluoromethane (CFC-11), dichlorodifluoromethane (CFC-12), and trichlorotrifluoroethane (CFC-113) and sulfur hexafluoride (SF 6 ); and hydrogen stable isotopic composition (δ 2 H) and oxygen isotopic composition (δ 18 O) of water. The data include an up to 14-year time series record of monthly sampling at five springs collected between 1995 and 2013. The measurements included temperature, specific conductance, pH, and discharge recorded at 30-minute intervals. Atmospheric mixing ratios of CFC-11, CFC-12, CFC-113, trifluorobromomethane (CF 3 Br), SF 6 , and trifluoromethyl sulfur pentafluoride (SF 5 CF 3 ) in air from the Big Meadows Air Monitoring Station, Shenandoah National Park, were measured at approximately weekly intervals from September 1995 through March 2014. Additional data include monthly (between May 2001 and August 2003) measurements of temperature, N 2 , O 2 , Ar, CO 2 , CFC-12, CFC-11, CFC-113, and SF 6 concentrations in unsaturated-zone air from seven multilevel piezometers in Shenandoah National Park and at the U.S. Geological Survey National Center in Reston, Virginia. All samples were analyzed at the U.S. Geological Survey Laboratories in Reston, Virginia.

Virginia↗
USGS1999

Trends in precipitation and stream-water chemistry in the northeastern United States, water years 1984-96

Trends in precipitation and stream-water chemistry during water years 1984-96 were examined at eight precipitation monitoring sites and five nearby streams operated by the U.S. Geological Survey in the northeastern United States. The statistical analyses indicate the following: 1)Stream-water sulfate (SO4) concentrations decreased at seven of eight precipitation monitoring sites and in each of five streams. 2)Calcium plus magnesium (Ca + Mg) concentrations decreased at seven of eight precipitation monitoring sites and in three of five streams. 3)Precipitation acidity decreased at five of eight precipitation monitoring sites, but alkalinity increased in only one stream. These results indicate that decreases in atmospheric deposition of SO4 have resulted in decreased precipitation acidity. The chemical response of stream water to changes in precipitation chemistry was complex. Decreases in stream-water SO4 concentrations generally matched decreases of precipitation SO4. In stream water, increases in alkalinity were uncommon because decreases in SO4 concentrations often were accompanied by decreases in Ca + Mg concentrations. The decreases in Ca + Mg concentrations might be related to depletion of base cations from soil caused by long-term exposure to acidic deposition. Increases in streamwater alkalinity might not occur until rates of acidic deposition are reduced to substantially less than the rate of cation resupply by weathering and atmospheric deposition. In areas where forests are aggrading, recovery of stream-water alkalinity will be delayed further because of the acidifying effect of biomass accumulation.

Fact Sheet↗
USGS1998

Nutrient sources within the Upper Mississippi River Basin, Minnesota and Wisconsin, 1991-93

The amount of nutrients contained in fertilizer, livestock manure, municipal wastewater, atmospheric deposition, and legume residues were quantified in each of the major drainage basins within the Upper Mississippi River Basin study unit (fig. 1) as part of the U.S. Geological Survey's National Water-Quality Assessment Program. These sources of nutrients may potentially affect surface- and ground-water quality, so knowledge about the relative importance of each source may assist in the management of surface and ground waters within the study unit. The relative importance of each nutrient source was expected to vary among each of the four drainage basins due to differences in land use across the study unit. Fertilizer and livestock manure were potentially large sources of nitrogen and phosphorus in each of the four drainage basins. However, nitrogen in legume residues was a more important source in the Upper Mississippi, St. Croix, and Lower Mississippi River Basins because hay comprised a larger part of the total acreage of crops grown in these basins. Atmospheric deposition comprised a larger percentage of the nitrogen sources in the St. Croix River Basin compared to the other three drainage basins probably because amounts of the other sources are relatively low. Nitrogen and phosphorus yields in streams were greatest in the Lower Mississippi River Basin and the Minnesota River Basin, where amounts of nonpoint sources of these constituents also were the greatest per square mile.

Minnesota, Wisconsin↗
USGS2023

Geologic carbon management options for the North Atlantic-Appalachian Region

Introduction The U.S. Geological Survey (USGS) North Atlantic-Appalachian Region is developing the regionwide capacity to provide timely science support for decision-makers attempting to enhance carbon removal, sequestration, and emissions mitigation to meet national atmospheric carbon reduction goals. The U.S. Environmental Protection Agency (EPA) reported that in 2021, the fourteen States and the District of Columbia in the northeastern region account about for approximately 18 percent of the total national greenhouse gas (GHG) emissions. This Fact Sheet provides a summary of USGS science information and ongoing and new investigations or data-collection programs that may help the northeastern region decrease the release of carbon-containing GHG to the atmosphere.

Connecticut, Delaware, Maine, Maryland, Massachuse↗
USGS1996

Environmental behavior and fate of methyl tert-butyl ether (MTBE)

When gasoline that has been oxygenated with methyl tert-butyl ether (MTBE) comes in contact with water, large amounts of MTBE can dissolve; at 25 degrees Celsius the water solubility of MTBE is about 5,000 milligrams per liter for a gasoline that is 10 percent MTBE by weight. In contrast, for a nonoxygenated gasoline, the total hydrocarbon solubility in water is typically about 120 milligrams per liter. MTBE sorbs only weakly to soil and aquifer materials; therefore, sorption will not significantly retard MTBE's transport by ground water. In addition, MTBE generally resists degradation in ground water. The half-life of MTBE in the atmosphere can be as short as 3 days in a regional airshed. MTBE in the air tends to partition into atmospheric water, including precipitation. However, washout of gas-phase MTBE by precipitation would not, by itself, greatly alter the gas-phase concentration of the compound in the air. The partitioning of MTBE to precipitation is nevertheless strong enough to allow for up to 3 micrograms per liter or more inputs of MTBE to surface and ground water.

Fact Sheet↗
USGS2025

PFAS sampling activities in the U.S. Geological Survey national networks

Per- and polyfluoroalkyl substances (PFAS), frequently called “forever chemicals,” are used for a wide variety of industrial purposes and are often found in common household and industrial items such as firefighting foams, non-stick cookware, and water-resistant materials. The contamination of water, air, and soil by PFAS is a national and global issue due to their widespread occurrence in multiple applications and resistance to biodegradation and other traditional treatment processes. Research indicates that many PFAS can be emitted to the atmosphere and transported and deposited long distances from the source. The U.S. Geological Survey (USGS) Water Resources Mission Area received funding to implement a national-scale sampling effort to assess PFAS occurrence. To follow agency directives, the National Water Quality Network (NWQN) added PFAS sample monitoring for both surface water and groundwater, and also added PFAS monitoring to selected sites in the National Atmospheric Deposition Program (NADP).

General Information Product↗