USGS Science⌕ Search

SEARCH · USGS Science

Results for “Atmosphere”

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 1,117 records · Page 62Linked to original sources

A new technique for surface and shallow subsurface paleobarometry using fluid inclusions: An example from the Upper Ordovician Viola Formation, Kansas, USA

This research illustrates a new approach for paleobarometry employing heterogeneously entrapped fluid inclusions to determine timing and depth of diagenesis. Heterogeneously entrapped fluid inclusions (gas + water) in vug-filling quartz from the Upper Ordovician Viola Formation in the Midcontinent of the United States were analyzed for their internal pressure with a fluid-inclusion crushing stage. The free gas in fluid inclusions was entrapped at near-surface temperature, as indicated by the presence of all-liquid fluid inclusions and fluid inclusions with low homogenization temperatures ( <40??C). Crushing the crystal and measuring the change in bubble size determines the pressure of entrapment directly. Heterogeneous trapping is indicated by widely varying L:V ratios, from all-liquid to vapor-rich. Gas bubbles in most fluid inclusions analyzed expanded upon release to atmospheric pressure, but some collapsed. A mode of 1.5 to 2.0 atm internal pressure was indicated by the crushing runs, but pressures up to 42.9 atm were recorded. Quartz precipitation and associated fluid-inclusion entrapment therefore occurred over a wide depth-range, but principally at depths of approximately 10 m. Crushing runs done in kerosene confirmed the presence of hydrocarbon gases in most of these inclusions, and bulk analyses of gases in the quartz by quadrupole mass spectrometer revealed methane, ethane, and atmospheric gases. The hydrocarbon gases may have originated in deeper thermogenically mature sedimentary strata, and then leaked to the near-surface where they were entrapped in the precipitating quartz cement. Freezing data indicate an event of quartz precipitation from fluids of marine-fresh water intermediate salinity and other events of precipitation from more saline fluids. Considering the determined pressures, the precipitating fluids probably originated at surfaces of subaerial exposure (unconformities) and surfaces of evaporite precipitation in the overlying Silurian strata. Thus, saline inclusions most likely originated from sinking of saline surface waters during Silurian time. Lower-salinity fluids record fluxes of meteoric water during development of unconformities in the Silurian. This type of paleobarometric study may have application in many other sedimentary systems, provided low-temperature and heterogeneous entrapment of an immiscible gas phase can be demonstrated for the fluid-inclusion assemblages studied.

Chemical Geology↗

Onset of thermally induced gas convection in mine wastes

A mine waste dump in which active oxidation of pyritic materials occurs can generate a large amount of heat to form convection cells. We analyze the onset of thermal convection in a two-dimensional, infinite horizontal layer of waste rock filled with moist gas, with the top surface of the waste dump open to the atmosphere and the bedrock beneath the waste dump forming a horizontal and impermeable boundary. Our analysis shows that the thermal regime of a waste rock system depends heavily on the atmospheric temperature, the strength of the heat source and the vapor pressure.

International Journal of Heat and Mass Transfer↗

Eolian sediment responses to late Quaternary climate changes: Temporal and spatial patterns in the Sahara

This paper presents a compilation of eolian-based records of late Quaternary climate changes in the Sahara. Although the data are relatively sparse, when viewed as a whole, they reveal a general pattern of widespread eolian sediment mobilization prior to 11,000 cal. years BP, eolian sediment stabilization from 11,000 to 5000 cal. years BP, and a return to widespread eolian sediment mobilization after 5000 cal. years BP. Furthermore, an eolian-based record from southern Tunisia reveals the existence of millennial-scale changes in eolian sediment behavior. These millennial-scale variations provide examples of eolian sediment responses to climate changes at a scale intermediate between seasonal and orbital ('Milankovitch') changes, and they are also coincident with abrupt atmospheric and oceanic changes. The general synchroneity of the eolian stratigraphic records and their coincidence with various oceanic and atmospheric changes suggest that global forcing mechanisms have influenced late Quaternary eolian sediment behavior in the Sahara. ?? 2001 Elsevier Science B.V.

Palaeogeography, Palaeoclimatology, Palaeoecology↗

Unprecedented last-glacial mass accumulation rates determined by luminescence dating of loess from western Nebraska

A high-resolution chronology for Peoria (last glacial period) Loess from three sites in Nebraska, midcontinental North America, is determined by applying optically stimulated luminescence (OSL) dating to 35-50 ??m quartz. At Bignell Hill, Nebraska, an OSL age of 25,000 yr near the contact of Peoria Loess with the underlying Gilman Canyon Formation shows that dust accumulation occurred early during the last glacial maximum (LGM), whereas at Devil's Den and Eustis, Nebraska, basal OSL ages are significantly younger (18,000 and 21,000 yr, respectively). At all three localities, dust accumulation ended at some time after 14,000 yr ago. Mass accumulation rates (MARs) for western Nebraska, calculated using the OSL ages, are extremely high from 18,000 to 14,000 yr-much higher than those calculated for any other pre-Holocene location worldwide. These unprecedented MARs coincide with the timing of a mismatch between paleoenvironmental evidence from central North America, and the paleoclimate simulations from atmospheric global circulation models (AGCMs). We infer that the high atmospheric dust loading implied by these MARs may have played an important role, through radiative forcing, in maintaining a colder-than-present climate over central North America for several thousand years after summer insolation exceeded present-day values. ?? 2003 Elsevier Science (USA). All rights reserved.

Quaternary Research↗

Equipment and techniques for low-altitude aerial sensing of water-vapor concentration and movement

Progress in the development of equipment and techniques for making rapid measurements of moisture movement through the atmosphere over a large area is described. Airborne sensing elements measure relative humidity, temperature, and air currents. These data are telemetered to a ground-based station and recorded. A radar unit tracks the aircraft and electronically plots its position on a base map of the area being studied. Thus the distribution of atmospheric conditions can be directly related to the underlying terrain and vegetation features.

Remote Sensing of Environment↗

Heavy metals in wild rice from northern Wisconsin

Wild rice grain samples from various parts of the world have been found to have elevated concentrations of heavy metals, raising concern for potential effects on human health. It was hypothesized that wild rice from north-central Wisconsin could potentially have elevated concentrations of some heavy metals because of possible exposure to these elements from the atmosphere or from water and sediments. In addition, no studies of heavy metals in wild rice from Wisconsin had been performed, and a baseline study was needed for future comparisons. Wild rice plants were collected from four areas in Bayfield, Forest, Langlade, Oneida, Sawyer and Wood Counties in September, 1997 and 1998 and divided into four plant parts for elemental analyses: roots, stems, leaves and seeds. A total of 194 samples from 51 plants were analyzed across the localities, with an average of 49 samples per part depending on the element. Samples were cleaned of soil, wet digested, and analyzed by ICP for Ag, As, Cd, Cr, Cu, Hg, Mg, Pb, Se and Zn. Roots contained the highest concentrations of Ag, As, Cd, Cr, Hg, Pb, and Se. Copper was highest in both roots and seeds, while Zn was highest just in seeds. Magnesium was highest in leaves. Seed baseline ranges for the 10 elements were established using the 95% confidence intervals of the medians. Wild rice plants from northern Wisconsin had normal levels of the nutritional elements Cu, Mg and Zn in the seeds. Silver, Cd, Hg, Cr, and Se were very low in concentration or within normal limits for food plants. Arsenic and Pb, however, were elevated and could pose a problem for human health. The pathway for As, Hg and Pb to the plants could be atmospheric.

Wisconsin↗

Seasonal estimates of riparian evapotranspiration using remote and in situ measurements

In many semi-arid basins during extended periods when surface snowmelt or storm runoff is absent, groundwater constitutes the primary water source for human habitation, agriculture and riparian ecosystems. Utilizing regional groundwater models in the management of these water resources requires accurate estimates of basin boundary conditions. A critical groundwater boundary condition that is closely coupled to atmospheric processes and is typically known with little certainty is seasonal riparian evapotranspiration ET). This quantity can often be a significant factor in the basin water balance in semi-arid regions yet is very difficult to estimate over a large area. Better understanding and quantification of seasonal, large-area riparian ET is a primary objective of the Semi-Arid Land-Surface-Atmosphere (SALSA) Program. To address this objective, a series of interdisciplinary experimental Campaigns were conducted in 1997 in the San Pedro Basin in southeastern Arizona. The riparian system in this basin is primarily made up of three vegetation communities: mesquite (Prosopis velutina), sacaton grasses (Sporobolus wrightii), and a cottonwood (Populus fremontii)/willow (Salix goodingii) forest gallery. Micrometeorological measurement techniques were used to estimate ET from the mesquite and grasses. These techniques could not be utilized to estimate fluxes from the cottonwood/willow (C/W) forest gallery due to the height (20-30 m) and non-uniform linear nature of the forest gallery. Short-term (2-4 days) sap flux measurements were made to estimate canopy transpiration over several periods of the riparian growing season. Simultaneous remote sensing measurements were used to spatially extrapolate tree and stand measurements. Scaled C/W stand level sap flux estimates were utilized to calibrate a Penman-Monteith model to enable temporal extrapolation between Synoptic measurement periods. With this model and set of measurements, seasonal riparian vegetation water use estimates for the riparian corridor were obtained. To validate these models, a 90-day pre-monsoon water balance over a 10 km section of the river was carried out. All components of the water balance, including riparian ET, were independently estimated. The closure of the water balance was roughly 5% of total inflows. The ET models were then used to provide riparian ET estimates over the entire corridor for the growing season. These estimates were approximately 14% less than those obtained from the most recent groundwater model of the basin for a comparable river reach.

Conference Paper↗

Modeling hyporheic zone processes

Stream biogeochemistry is influenced by the physical and chemical processes that occur in the surrounding watershed. These processes include the mass loading of solutes from terrestrial and atmospheric sources, the physical transport of solutes within the watershed, and the transformation of solutes due to biogeochemical reactions. Research over the last two decades has identified the hyporheic zone as an important part of the stream system in which these processes occur. The hyporheic zone may be loosely defined as the porous areas of the stream bed and stream bank in which stream water mixes with shallow groundwater. Exchange of water and solutes between the stream proper and the hyporheic zone has many biogeochemical implications, due to differences in the chemical composition of surface and groundwater. For example, surface waters are typically oxidized environments with relatively high dissolved oxygen concentrations. In contrast, reducing conditions are often present in groundwater systems leading to low dissolved oxygen concentrations. Further, microbial oxidation of organic materials in groundwater leads to supersaturated concentrations of dissolved carbon dioxide relative to the atmosphere. Differences in surface and groundwater pH and temperature are also common. The hyporheic zone is therefore a mixing zone in which there are gradients in the concentrations of dissolved gasses, the concentrations of oxidized and reduced species, pH, and temperature. These gradients lead to biogeochemical reactions that ultimately affect stream water quality. Due to the complexity of these natural systems, modeling techniques are frequently employed to quantify process dynamics.

Advances in Water Resources↗

Basin level statistical properties of topographic index for North America

For land&ndash;atmosphere interaction studies several Topmodel based land-surface schemes have been proposed. For the implementation of such models over the continental (and global) scales, statistical properties of the topographic indices are derived using GTOPO30 (30-arc-second; 1 km resolution) DEM data for North America. River basins and drainage network extracted using this dataset are overlaid on computed topographic indices for the continent and statistics are extracted for each basin. A total of 5020 basins are used to cover the entire continent with an average basin size of 3640 km 2 . Typically, the first three statistical moments of the distribution of the topographic indices for each basin are required for modeling. Departures of these statistical moments to those obtained using high resolution data have important implications for the prediction of soil-moisture states in the hydrologic models and consequently on the dynamics of the land&ndash;atmosphere interaction. It is found that a simple relationship between the statistics obtained at the 1 km and 90 m resolutions can be developed. The mean, standard deviation, skewness, L-scale and L-skewness all show approximate linear relationships between the two resolutions making it possible to use the moment estimates from the GTOPO30 data for hydrologic studies by applying a simple linear downscaling scheme. This significantly increases the utility value of the GTOPO30 datasets for hydrologic modeling studies.

Advances in Water Resources↗

Summer snow determines the depth to ice-cemented ground under dry permafrost in Antarctica

Dry permafrost underlain by ice-cemented permafrost has been reported in several locations in Antarctica. Initially thought to be relic ice, it is now understood that this subsurface ice is in equilibrium with the surface conditions, although it is not in equilibrium with the atmosphere. We use year-round data from University Valley in the Dry Valleys and Elephant Head in the Ellsworth Mountains to investigate the seasonal variations in water vapour flux that control the depth to the ice table under dry permafrost. Our analysis shows that the mean annual water vapour density of the soil surface exceeds the atmospheric value by a factor of up to ~2 due to summer snow. The attenuation and phase shift of the annual temperature cycle with depth result in colder temperatures at the ice table than at the surface of the soil in summer. We conclude that this temperature gradient, combined with the summer snow, provides the flux of water to the ice table necessary to maintain the ice. In University Valley, reducing the snow days by 40% moves the stability depth of the ice table from 42 to 66 cm. Increasing the snow days by 60% shifts the ice table to 17 cm. These variations can explain the observed gradient in the depth to the ice table in University Valley.

Antarctic Science↗

The US EPA’s National Nutrient Inventory: Critical shifts in US nutrient pollution sources from 1987 to 2017

Efforts to constrain the negative environmental impacts of excess nitrogen (N) and phosphorus (P) are costly and challenging, due in part to inconsistent reporting of nutrient sources at temporal and spatial scales relevant for local decision making. To meet this challenge, the U.S. Environmental Protection Agency’s National Nutrient Inventory provides estimates of major agricultural, urban, atmospheric, and natural nutrient fluxes for the contiguous United States at county and HUC12 scales annually from 1987 (from 1950 for agriculture) to 2017. Since the late 1980s, total N emissions and atmospheric N deposition have declined 22% and 15%, respectively, despite increased agricultural emissions. Over the same period, municipal wastewater N and P loads remained largely stable, despite population increases, through wastewater treatment upgrades and the phaseout of phosphorus-containing detergents. Improved agricultural efficiency allowed for dramatic increases in agricultural production and crop harvest since 1987 (∼25% for N and P), with little change in surplus nutrients left on fields. Overall, a combination of innovative technologies and management has stemmed or even decreased major sources of nutrient pollution to the environment over the last several decades, representing an important shift that, if continued, may contribute to improved air, land, and water quality and human health.

contiguous United States↗

Methane clumped isotopologue variability from ebullition in a mid-latitude lake

Methane is a greenhouse gas and is an important component of carbon cycling in freshwater environments. Isotope ratios of methane ( 13 C/ 12 C and D/H) are used extensively as tracers to identify methane sources. Recent advances in the measurement of clumped methane isotopologues ( 13 CH 3 D, 12 CH 2 D 2 ) offer new opportunities to constrain sources and sinks of atmospheric methane. Previous measurements of clumped methane isotopologues from freshwater environments have been spatially and temporally limited. The abundance of 13 CH 3 D and methane flux from ebullition in the deep basin of Upper Mystic Lake were measured from May to November 2021 to characterize the source isotopologue signatures and methane fluxes for mid-latitude lakes. The trends in δ 13 C and δD values support decreased methane oxidation in the early summer compared to fall. The Δ 13 CH 3 D values from this study range from 2.0 to 4.2‰, reflecting methane oxidation occurring anaerobically in lake sediments and euxinic bottom waters at sample sites. The relatively large variation in the Δ 13 CH 3 D values observed within this lake basin aligns with previous observations of bubbles from arctic lakes. The values of Δ 13 CH 3 D do not correlate with methane flux, suggesting that Δ 13 CH 3 D measurements from background ebullition are not sensitive as a proxy for ebullition rates. This study presents a uniquely large ( n = 40) set of freshwater Δ 13 CH 3 D values from a single lake basin, which we use to recommend a sampling strategy of ≥9 samples to constrain the Δ 13 CH 3 D source signal within ∼0.5‰ from similar environments. This data demonstrates the utility of clumped methane isotopologues to gain insights into local biogeochemical processes from field studies and points to the challenge of using clumped isotopologue measurements to constrain global freshwater–methane sources to the atmosphere.

ACS Earth and Space Chemistry↗

Beryllium-7 as a tracer of short-term sediment deposition and resuspension in the Fox River Wisconsin

Short-term (∼monthly) sediment deposition and resuspension rates of surficial bed sediments in two PCB-laden impoundments on the Fox River, WI, were determined in the summer and fall of 1998 using 7 Be, a naturally occurring radioisotope produced in the atmosphere. Decay-corrected activities and inventories of 7 Be were measured in bed sediment and in suspended particles. Beryllium-7 activities generally decreased with depth in the top 5−10 cm of sediments and ranged from undetectable to ∼0.9 pCi cm - 3 . Inventories of 7 Be, calculated from the sum of activities from all depths, ranged from 0.87 to 3.74 pCi cm - 2 , and the values covaried between sites likely reflecting a common atmospheric input signal. Activities of 7 Be did not correlate directly with rainfall. Partitioning the 7 Be flux into “new” and “residual” components indicated that net deposition was occurring most of the time during the summer. Net erosion, however, was observed at the upstream site from the final collection in the fall. This erosion event was estimated to have removed 0.10 g (cm of sediment) - 2 , corresponding to ∼0.5 cm of sediment depth, and ∼6−10 kg of polychlorinated biphenyls (PCBs) over the whole deposit. Short-term accumulation rates were up to ∼130 times higher than the long-term rates calculated from 137 Cs profiles, suggesting an extremely dynamic sediment transport environment, even within an impounded river system.

Environmental Science & Technology↗

Snow chemistry of the Cascade-Sierra Nevada Mountains

This investigation assesses geographic variations in atmospheric deposition in Washington, Oregon, and California using snow cores from the Cascade-Sierra Nevada Mountains, collected from late February to mid-March 1983. A statistical analysis of the analytical and sampling precision was made. The snowpack in the higher Cascades and Sierra Nevada is not strongly influenced by anthropogenic activities at present. The pH of snow samples ranges from 5.11 to 5.88. Sulfate and nitrate correlate with H+ in some segments of the sample traverse. The SO4 data show apparent influence from major source areas in Washington and California; nitrate does not. An apparent decrease in NH4 in snow in Washington and California suggests atmospheric interactions resulting in the removal of NH4. The NH4 reduction raises questions about nutrient supply to the mountain vegetation. Heavy-metal correlations included Cd, Cu, and Fe with Pb, and Mn with K and DOC, among others. No correlation was found between constituents and snow-water content.

California, Oregon, Washington↗

Tire-wear particles as a source of zinc to the environment

Tire-tread material has a zinc (Zn) content of about 1 wt %. The quantity of tread material lost to road surfaces by abrasion has not been well characterized. Two approaches were used to assess the magnitude of this nonpoint source of Zn in the U.S. for the period 1936−1999. In the first approach, tread-wear rates from the automotive engineering literature were used in conjunction with vehicle distance-driven data from the U.S. Department of Transportation to determine Zn releases. A second approach calculated this source term from the volume of tread lost during lifetime tire wear. These analyses showed that the quantity of Zn released by tire wear in the mid-1990s was of the same magnitude as that released from waste incineration. For 1999, the quantity of Zn released by tire wear in the U.S. is estimated to be 10 000−11 000 metric tons. A specific case study focused on Zn sources and sinks in an urban−suburban watershed (Lake Anne) in the Washington, DC, metropolitan area for a time period of the late 1990s. The atmospheric flux of total Zn (wet deposition) to the watershed was 2 μg/cm 2 /yr. The flux of Zn to the watershed estimated from tire wear was 42 μg/cm 2 /yr. The measured accumulation rate of total Zn in age-dated sediment cores from Lake Anne was 27 μg/cm 2 /yr. These data suggest that tire-wear Zn inputs to urban−suburban watersheds can be significantly greater than atmospheric inputs, although the watershed appears to retain appreciable quantities of vehicular Zn inputs.

Environmental Science & Technology↗

Assessing the potential for re-emission of mercury deposited in precipitation from arid soils using a stable isotope

A solution containing 198 Hg in the form of HgCl 2 was added to a 4 m 2 area of desert soils in Nevada, and soil Hg fluxes were measured using three dynamic flux chambers. There was an immediate release of 198 Hg after it was applied, and then emissions decreased exponentially. Within the first 6 h after the isotope was added to the soil, ∼12 ng m - 2 of 198 Hg was emitted to the atmosphere, followed by a relatively steady flux of the isotope at 0.2 ± 0.2 ng m - 2 h - 1 for the remainder of the experiment (62 days). Over this time, ∼200 ng m - 2 or 2% of the 198 Hg isotope was emitted from the soil, and we estimate that ∼6% of the isotope would be re-emitted in a year's time. During the experiment, dry deposition of elemental Hg from the atmosphere was measured with an average deposition rate of 0.2 ± 0.1 ng m - 2 h - 1 . Emission of ambient Hg from the soil was observed after soil wetting with the isotope solution and after a storm event. However, the added moisture from the storm event did not affect 198 Hg flux. Results suggest that in this desert environment, where there is limited precipitation, Hg deposited by wet processes is not readily re-emitted and that dry deposition of elemental Hg may be an important process.

Environmental Science & Technology↗

Widespread presence of naturally occurring perchlorate in high plains of Texas and New Mexico

Perchlorate (ClO4-) occurrence in groundwater has previously been linked to industrial releases and the historic use of Chilean nitrate fertilizers. However, recently a number of occurrences have been identified for which there is no obvious anthropogenic source. Groundwater from an area of 155 000 km2 in 56 counties in northwest Texas and eastern New Mexico is impacted by the presence of ClO4-. Concentrations were generally low (<4 ppb), although some areas are impacted by concentrations up to 200 ppb. ClO4- distribution is not related to well type (public water system, domestic, agricultural, or water-table monitoring) or aquifer (Ogallala, Edward Trinity High Plains, Edwards Trinity Plateau, Seymour, or Cenozoic). Results from vertically nested wells strongly indicate a surface source. The source of ClO4- appears to most likely be atmospheric deposition. Evidence supporting this hypothesis primarily relates to the presence of ClO 4- in tritium-free older water, the lack of relation between land use and concentration distribution, the inability of potential anthropogenic sources to account for the estimated mass of ClO4-, and the positive relationship between conserved anions (e.g., IO3-, Cl-, SO4-2) and ClO4-. The ClO4- distribution appears to be mainly related to evaporative concentration and unsaturated transport. This process has led to higher ClO4- and other ion concentrations in groundwater where the water table is relatively shallow, and in areas with lower saturated thickness. Irrigation may have accelerated this process in some areas by increasing the transport of accumulated salts and by increasing the number of evaporative cycles. Results from this study highlight the potential for ClO4- to impact groundwater in arid and semiarid areas through long-term atmospheric deposition. ?? 2006 American Chemical Society.

Environmental Science & Technology↗

Differences in phosphorus and nitrogen delivery to the Gulf of Mexico from the Mississippi River Basin

Seasonal hypoxia in the northern Gulf of Mexico has been linked to increased nitrogen fluxes from the Mississippi and Atchafalaya River Basins, though recent evidence shows that phosphorus also influences productivity in the Gulf. We developed a spatially explicit and structurally detailed SPARROW water-quality model that reveals important differences in the sources and transport processes that control nitrogen (N) and phosphorus (P) delivery to the Gulf. Our model simulations indicate that agricultural sources in the watersheds contribute more than 70% of the delivered N and P. However, corn and soybean cultivation is the largest contributor of N (52%), followed by atmospheric deposition sources (16%); whereas P originates primarily from animal manure on pasture and rangelands (37%), followed by corn and soybeans (25%), other crops (18%), and urban sources (12%). The fraction of in-stream P and N load delivered to the Gulf increases with stream size, but reservoir trapping of P causes large local- and regional-scale differences in delivery. Our results indicate the diversity of management approaches required to achieve efficient control of nutrient loads to the Gulf. These include recognition of important differences in the agricultural sources of N and P, the role of atmospheric N, attention to P sources downstream from reservoirs, and better control of both N and P in close proximity to large rivers. ?? 2008 American Chemical Society.

Environmental Science & Technology↗