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Integrating the evidence for a terrestrial carbon sink caused by increasing atmospheric CO2

Atmospheric carbon dioxide concentration ([CO 2 ]) is increasing, which increases leaf‐scale photosynthesis and intrinsic water‐use efficiency. These direct responses have the potential to increase plant growth, vegetation biomass, and soil organic matter; transferring carbon from the atmosphere into terrestrial ecosystems (a carbon sink). A substantial global terrestrial carbon sink would slow the rate of [CO 2 ] increase and thus climate change. However, ecosystem CO 2 responses are complex or confounded by concurrent changes in multiple agents of global change and evidence for a [CO 2 ]‐driven terrestrial carbon sink can appear contradictory. Here we synthesize theory and broad, multidisciplinary evidence for the effects of increasing [CO 2 ] (iCO 2 ) on the global terrestrial carbon sink. Evidence suggests a substantial increase in global photosynthesis since pre‐industrial times. Established theory, supported by experiments, indicates that iCO 2 is likely responsible for about half of the increase. Global carbon budgeting, atmospheric data, and forest inventories indicate a historical carbon sink, and these apparent iCO 2 responses are high in comparison to experiments and predictions from theory. Plant mortality and soil carbon iCO 2 responses are highly uncertain. In conclusion, a range of evidence supports a positive terrestrial carbon sink in response to iCO 2 , albeit with uncertain magnitude and strong suggestion of a role for additional agents of global change.

New Phytologist

Structure of the atmosphere of Venus up to 110 kilometers: Preliminary results from the four Pioneer Venus entry probes

The four Pioneer Venus entry probes transmitted data of good quality on the structure of the atmosphere below the clouds. Contrast of the structure below an altitude of 50 kilometers at four widely separated locations was found to be no more than a few degrees Kelvin, with slightly warmer temperatures at 30° south latitude than at 5° or 60° north. The atmosphere was stably stratified above 15 or 20 kilometers, indicating that the near-adiabatic state is maintained by the general circulation. The profiles move from near-adiabatic toward radiative equilibrium at altitudes above 40 kilometers. There appears to be a region of vertical convection above the dense cloud deck, which lies at 47.5 to 49 kilometers and at temperature levels near 360 K. The atmosphere is nearly isothermal around 100 kilometers (175 to 180 K) and appears to exhibit a sizable temperature wave between 60 and 70 kilometers. This is where the 4-day wind is believed to occur. The temperature wave may be related to some of the wavelike phenomena seen in Mariner 10 ultraviolet photographs.

Science

Increasing rates of atmospheric mercury deposition in midcontinental North America

Mercury contamination of remote lakes has been attributed to increasing deposition of atmospheric mercury, yet historic deposition rates and inputs from terrestrial sources are essentially unknown. Sediments of seven headwater lakes in Minnesota and Wisconsin were used to reconstruct regional modern and preindustrial deposition rates of mercury. Whole-basin mercury fluxes, determined from lake-wide arrays of dated cores, indicate that the annual deposition of atmospheric mercury has increased from 3.7 to 12.5 micrograms per square meter since 1850 and that 25 percent of atmospheric mercury deposition to the terrestrial catchment is exported to the lake. The deposition increase is similar among sites, implying regional or global sources for the mercury entering these lakes.

Science

Lake-atmosphere feedbacks associated with paleolakes Bonneville and Lahontan

A high-resolution, regional climate model nested within a general circulation model was used to study the interactions between the atmosphere and the large Pleistocene lakes in the Great Basin of the United States. Simulations for January and July 18,000 years ago indicate that moisture provided by synoptic-scale atmospheric circulation features was the primary component of the hydrologic budgets of Lakes Lahontan and Bonneville. In addition, lake-generated precipitation was a substantial component of the hydrologic budget of Lake Bonneville at that time. This local lake-atmosphere interaction may help explain differences in the relative sizes of these lakes 18,000 years ago.

Great Basin

Atmospheric waves and global seismoacoustic observations of the January 2022 Hunga eruption, Tonga

The 15 January 2022 climactic eruption of Hunga volcano, Tonga, produced an explosion in the atmosphere of a size that has not been documented in the modern geophysical record. The event generated a broad range of atmospheric waves observed globally by various ground-based and spaceborne instrumentation networks. Most prominent was the surface-guided Lamb wave (≲0.01 hertz), which we observed propagating for four (plus three antipodal) passages around Earth over 6 days. As measured by the Lamb wave amplitudes, the climactic Hunga explosion was comparable in size to that of the 1883 Krakatau eruption. The Hunga eruption produced remarkable globally detected infrasound (0.01 to 20 hertz), long-range (~10,000 kilometers) audible sound, and ionospheric perturbations. Seismometers worldwide recorded pure seismic and air-to-ground coupled waves. Air-to-sea coupling likely contributed to fast-arriving tsunamis. Here, we highlight exceptional observations of the atmospheric waves.

Hunga volcano

Evidence of wildfires and elevated atmospheric oxygen at the Frasnian–Famennian boundary in New York (USA): Implications for the Late Devonian mass extinction

The Devonian Period experienced significant fluctuations of atmospheric oxygen (O 2 ) levels (∼25–13%), for which the extent and timing are debated. Also characteristic of the Devonian Period, at the Frasnian–Famennian (F–F) boundary, is one of the “big five” mass extinction events of the Phanerozoic. Fossilized charcoal (inertinite) provides a record of wildfire events, which in turn can provide insight into the evolution of terrestrial ecosystems and the atmospheric composition. Here, we report organic petrology, programmed pyrolysis analysis, major and trace element analyses, and initial osmium isotope (Os i ) stratigraphy from five sections of Upper Devonian (F–F interval) from western New York, USA. These data are discussed to infer evidence of a wildfire event at the F–F boundary. Based on the evidence for a wildfire at the F–F boundary we also provide an estimate of atmospheric O 2 levels of ∼23–25% at this interval, which is in agreement with the models that predict elevated p O 2 levels during the Late Devonian. This, coupled with our Os isotope records, support the currently published Os i data that lacks any evidence for an extra-terrestrial impact or volcanic event at the F–F interval, and therefore to act as a trigger for the F–F mass extinction. The elevated O 2 level at the F–F interval inferred from this study supports the hypothesis that p CO 2 drawdown and associated climate cooling may have acted as a driving mechanism of the F–F mass extinction.

New York

A multiscale and multidisciplinary investigation of ecosystem-atmosphere CO 2 exchange over the rocky mountains of colorado

A field study combined with modeling investigation demonstrated that the organization of CO2 transport by mountain terrain strongly affects the regional CO2 budget. Atmospheric dynamics can lead to complicated flows generated by inhomogeneous landscapes, topography or synoptic weather systems. The field campaign conducted of a ground deployment, the Carbon in the Mountain Experiment (CME04), and an aircraft deployment of the national Center for Atmospheric Research (NCAR) C-130, the Airborne Carbon in the Mountains Experiment (ACME04) over the period of spring to fall of 2004 to cover the seasonal variation of ecosystem-atmosphere carbon exchange. The role of the mountain circulation in CO2 transport can be played over seemingly flat terrain by mesoscale flows generated by various physical processes. The three dimensional observation strategy considered can also be applied over flat terrain.

Bulletin of the American Meteorological Society

Patterns and drivers of atmospheric river precipitation and hydrologic impacts across the western United States

Atmospheric rivers (ARs) significantly influence precipitation and hydrologic variability in many areas of the world, including the western United States. As ARs are increasingly recognized by the research community and the public, there is a need to more precisely quantify and communicate their hydrologic impacts, which can vary from hazardous to beneficial depending on location and on the atmospheric and land surface conditions prior to and during the AR. This study leverages 33 years of atmospheric and hydrologic data for the western United States to 1) identify how water vapor amount, wind direction and speed, temperature, and antecedent soil moisture conditions influence precipitation and hydrologic responses (runoff, recharge, and snowpack) using quantile regression and 2) identify differences in hydrologic response types and magnitudes across the study region. Results indicate that water vapor amount serves as a primary control on precipitation amounts. Holding water vapor constant, precipitation amounts vary with wind direction, depending on location, and are consistently greater at colder temperatures. Runoff efficiencies further covary with temperature and antecedent soil moisture, with precipitation falling as snow and greater available water storage in the soil column mitigating flood impacts of large AR events. This study identifies the coastal and maritime mountain ranges as areas with the greatest potential for hazardous flooding and snowfall impacts. This spatially explicit information can lead to better understanding of the conditions under which ARs of different precipitation amounts are likely to be hazardous at a given location.

Journal of Hydrometeorology

Transport of tritium contamination to the atmosphere in an arid environment

Soil–plant–atmosphere interactions strongly influence water movement in desert unsaturated zones, but little is known about how such interactions affect atmospheric release of subsurface water-borne contaminants. This 2-yr study, performed at the U.S. Geological Survey's Amargosa Desert Research Site in southern Nevada, quantified the magnitude and spatiotemporal variability of tritium (3H) transport from the shallow unsaturated zone to the atmosphere adjacent to a low-level radioactive waste (LLRW) facility. Tritium fluxes were calculated as the product of 3H concentrations in water vapor and respective evaporation and transpiration water-vapor fluxes. Quarterly measured 3H concentrations in soil water vapor and in leaf water of the dominant creosote-bush [ Larrea tridentat a (DC.) Coville] were spatially extrapolated and temporally interpolated to develop daily maps of contamination across the 0.76-km2 study area. Maximum plant and root-zone soil concentrations (4200 and 8700 Bq L−1, respectively) were measured 25 m from the LLRW facility boundary. Continuous evaporation was estimated using a Priestley–Taylor model and transpiration was computed as the difference between measured eddy-covariance evapotranspiration and estimated evaporation. The mean evaporation/transpiration ratio was 3:1. Tritium released from the study area ranged from 0.12 to 12 μg d−1 and totaled 1.5 mg (8.2 × 1010 Bq) over 2 yr. Tritium flux variability was driven spatially by proximity to 3H source areas and temporally by changes in 3H concentrations and in the partitioning between evaporation and transpiration. Evapotranspiration removed and limited penetration of precipitation beneath native vegetation and fostered upward movement and release of 3H from below the root zone.

Vadose Zone Journal

Hydrologic, Water-Quality, Sediment Transport, and Bulk Atmospheric-Deposition Data, Guanella Pass Area, Colorado, October 1, 1994, through September 30, 1997

The hydrology and water quality of streams and lakes in the Guanella Pass area could be affected by the proposed reconstruction of the existing road over Guanella Pass between Georgetown and Grant, Colo. Data were collected during water years 1995 through 1997 (October 1, 1994, through September 30, 1997) that describe the preconstruction hydrology, water quality, sediment transport, and bulk atmospheric deposition in the Guanella Pass study area with most data being collected primarily during water years 1996-97. Data were collected at 17 stream sites, 7 road-runoff sites, 10 ground-water sites, 3 lake sites, 1 reservoir site, 2 snow-precipitation sites, and 4 bulk atmospheric-deposition sites. Data include onsite measurements of streamflow, specific conductance, pH, water temperature, turbidity, barometric pressure, and dissolved oxygen; concentrations of major ions, nutrients, and trace elements; organic carbon and trace organic compounds; suspended-sediment concentration and particle-size analyses; field measurement and depth profiles, and chlorophyll concentrations in lakes and reservoirs; trace element, nutrient, and trace organic (semi-volatiles, PCBs, and insecticides) analyses of lake and reservoir bottom sediment; and bulk atmospheric deposition rates of solids. Daily values for streamflow, maximum and minimum water temperature, specific conductance, and suspended sediment were computed at seven streamflow-monitoring stations located along South Clear Creek, Leavenworth Creek, Duck Creek, Geneva Creek, and Deer Creek.

Open-File Report

Fission products in National Atmospheric Deposition Program—Wet deposition samples prior to and following the Fukushima Dai-Ichi Nuclear Power Plant incident, March 8?April 5, 2011

Radioactive isotopes I-131, Cs-134, or Cs-137, products of uranium fission, were measured at approximately 20 percent of 167 sampled National Atmospheric Deposition Program monitoring sites in North America (primarily in the contiguous United States and Alaska) after the Fukushima Dai-Ichi Nuclear Power Plant incident on March 12, 2011. Samples from the National Atmospheric Deposition Program were analyzed for the period of March 8-April 5, 2011. Calculated 1- or 2-week radionuclide deposition fluxes at 35 sites from Alaska to Vermont ranged from 0.47 to 5,100 Becquerels per square meter during the sampling period of March 15-April 5, 2011. No fission-product isotopes were measured in National Atmospheric Deposition Program samples obtained during March 8-15, 2011, prior to the arrival of contaminated air in North America.

Puerto Rico;U.S. Virgin Islands;North America

Evaluation of coral pathogen growth rates after exposure to atmospheric African dust samples

Laboratory experiments were conducted to assess if exposure to atmospheric African dust stimulates or inhibits the growth of four putative bacterial coral pathogens. Atmospheric dust was collected from a dust-source region (Mali, West Africa) and from Saharan Air Layer masses over downwind sites in the Caribbean [Trinidad and Tobago and St. Croix, U.S. Virgin Islands (USVI)]. Extracts of dust samples were used to dose laboratory-grown cultures of four putative coral pathogens: Aurantimonas coralicida (white plague type II), Serratia marcescens (white pox), Vibrio coralliilyticus , and V. shiloi (bacteria-induced bleaching). Growth of A. coralicida and V. shiloi was slightly stimulated by dust extracts from Mali and USVI, respectively, but unaffected by extracts from the other dust sources. Lag time to the start of log-growth phase was significantly shortened for A. coralicida when dosed with dust extracts from Mali and USVI. Growth of S. marcescens and V. coralliilyticus was neither stimulated nor inhibited by any of the dust extracts. This study demonstrates that constituents from atmospheric dust can alter growth of recognized coral disease pathogens under laboratory conditions.

Caribbean Sea

Sensitivity of alpine and subalpine lakes to acidification from atmospheric deposition in Grand Teton National Park and Yellowstone National Park, Wyoming

The sensitivity of 400 lakes in Grand Teton and Yellowstone National Parks to acidification from atmospheric deposition of nitrogen and sulfur was estimated based on statistical relations between acid-neutralizing capacity concentrations and basin characteristics to aid in the design of a long-term monitoring plan for Outstanding Natural Resource Waters. Acid-neutralizing capacity concentrations that were measured at 52 lakes in Grand Teton and 23 lakes in Yellowstone during synoptic surveys were used to calibrate the statistical models. Three acid-neutralizing capacity concentration bins (bins) were selected that are within the U.S. Environmental Protection Agency criteria of sensitive to acidification; less than 50 microequivalents per liter (?eq/L) (0-50), less than 100 ?eq/L (0-100), and less than 200 ?eq/L (0-200). The development of discrete bins enables resource managers to have the ability to change criteria based on the focus of their study. Basin-characteristic information was derived from Geographic Information System data sets. The explanatory variables that were considered included bedrock type, basin slope, basin aspect, basin elevation, lake area, basin area, inorganic nitrogen deposition, sulfate deposition, hydrogen ion deposition, basin precipitation, soil type, and vegetation type. A logistic regression model was developed and applied to lake basins greater than 1 hectare in Grand Teton (n = 106) and Yellowstone (n = 294). A higher percentage of lakes in Grand Teton than in Yellowstone were predicted to be sensitive to atmospheric deposition in all three bins. For Grand Teton, 7 percent of lakes had a greater than 60-percent probability of having acid-neutralizing capacity concentrations in the 0-50 bin, 36 percent of lakes had a greater than 60-percent probability of having acid-neutralizing capacity concentrations in the 0-100 bin, and 59 percent of lakes had a greater than 60-percent probability of having acid-neutralizing capacity concentrations in the 0-200 bin. The elevation of the lake outlet and the area of the basin with northeast aspects were determined to be statistically significant and were used as the explanatory variables in the multivariate logistic regression model for the 0-100 bin. For Yellowstone, results indicated that 13 percent of lakes had a greater than 60-percent probability of having acid-neutralizing capacity concentrations in the 0-100 bin, and 27 percent of lakes had a greater than 60-percent probability of having acid-neutralizing capacity concentrations in the 0-200 bin. Only the elevation of the lake outlet was determined to be statistically significant and was used as the explanatory variable for the 0-100 bin. The lakes that exceeded 60-percent probability of having an acid-neutralizing capacity concentration in the 0-100 bin, and therefore had the greatest sensitivity to acidification from atmospheric deposition, are located at elevations greater than 2,790 meters in Grand Teton, and greater than 2,590 meters in Yellowstone.

Scientific Investigations Report

Atmospheric Deposition and Surface-Water Chemistry in Mount Rainier and North Cascades National Parks, U.S.A., Water Years 2000 and 2005-2006

High-elevation aquatic ecosystems in Mount Rainier and North Cascades National Parks are highly sensitive to atmospheric deposition of nitrogen and sulfur. Thin, rocky soils promote fast hydrologic flushing rates during snowmelt and rain events, limiting the ability of basins to neutralize acidity and assimilate nitrogen deposited from the atmosphere. Potential effects of nitrogen and sulfur deposition include episodic or chronic acidification of terrestrial and aquatic ecosystems. In addition, nitrogen deposition can cause eutrophication of water bodies and changes in species composition in lakes and streams. This report documents results of a study performed by the U.S. Geological Survey, in cooperation with the National Park Service, of the effects of atmospheric deposition of nitrogen and sulfur on surface-water chemistry in Mount Rainier and North Cascades National Parks. Inorganic nitrogen in wet deposition was highest in the vicinity of North Cascades National Park, perhaps due to emissions from human sources and activities in the Puget Sound area. Sulfur in wet deposition was highest near the Pacific coast, reflecting the influence of marine aerosols. Dry deposition generally accounted for less than 30 percent of wet plus dry inorganic nitrogen and sulfur deposition, but occult deposition (primarily fog) represents a potentially substantial unmeasured component of total deposition. Trend analyses indicate inorganic nitrogen in wet deposition was relatively stable during 1986-2005, but sulfur in wet deposition declined substantially during that time, particularly after 2001, when emissions controls were added to a large powerplant in western Washington. Surface-water sulfate concentrations at the study site nearest the powerplant showed a statistically significant decrease between 2000 and 2005-06, but there was no statistically significant change in alkalinity, indicating a delayed response in surface-water alkalinity. Seasonal patterns in surface-water chemistry and streamflow are strongly influenced by melting of seasonal snowpacks, which release large amounts of dilute, slightly acidic water to terrestrial and aquatic ecosystems during spring snowmelt. Concentrations of sulfate, alkalinity, and base cations in surface water declined rapidly during snowmelt, then gradually recovered during summer and fall. Preferential elution of acidic solutes from the snowpack at the beginning of snowmelt may cause episodic acidification in small alpine streams; evidence is provided by a stream sample collected at one of the sites during spring 2006 that was acidic (pH = 4.8, alkalinity = -18 microequivalents per liter) and had high concentrations of nitrate and sulfate and low concentrations of weathering products. Rain-on-snow events caused sharp declines in specific conductance, which was measured continuously using an in-stream sensor. A strong correlation was observed between measured specific conductance and measured alkalinity (r2 = 0.76), permitting estimation of alkalinity from specific-conductance data using a regression equation. Estimated alkalinity declined by an order of magnitude during the rain-on-snow events, in one case to 8 microequivalents per liter. Actual declines in alkalinity might be greater because the regression equation accounts only for dilution effects; at low concentrations, the relation between specific conductance and alkalinity is likely to be nonlinear and have a negative intercept (negative alkalinity). Thus, episodic acidification is possible during rain-on-snow events. The scale of episodic acidification is unknown, but if it occurs, it could have detrimental effects on aquatic life and amphibians. Historical lake-survey data indicate that most lakes are oligotrophic and have low nitrogen and phosphorus concentrations. Nitrogen limitation is more common in lakes in Mount Rainier National Park than in North Cascades National Park due to higher nitrate concentrations at North Cascades. T

Scientific Investigations Report

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

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

Scientific Investigations Report

Methods, quality assurance, and data for assessing atmospheric deposition of pesticides in the Central Valley of California

The U.S. Geological Survey monitored atmospheric deposition of pesticides in the Central Valley of California during two studies in 2001 and 2002–04. The 2001 study sampled wet deposition (rain) and storm-drain runoff in the Modesto, California, area during the orchard dormant-spray season to examine the contribution of pesticide concentrations to storm runoff from rainfall. In the 2002–04 study, the number and extent of collection sites in the Central Valley were increased to determine the areal distribution of organophosphate insecticides and other pesticides, and also five more sample types were collected. These were dry deposition, bulk deposition, and three sample types collected from a soil box: aqueous phase in runoff, suspended sediment in runoff, and surficial-soil samples. This report provides concentration data and describes methods and quality assurance of sample collection and laboratory analysis for pesticide compounds in all samples collected from 16 sites. Each sample was analyzed for 41 currently used pesticides and 23 pesticide degradates, including oxygen analogs (oxons) of 9 organophosphate insecticides. Analytical results are presented by sample type and study period. The median concentrations of both chloryprifos and diazinon sampled at four urban (0.067 micrograms per liter [μg/L] and 0.515 μg/L, respectively) and four agricultural sites (0.079 μg/L and 0.583 μg/L, respectively) during a January 2001 storm event in and around Modesto, Calif., were nearly identical, indicating that the overall atmospheric burden in the region appeared to be fairly similar during the sampling event. Comparisons of median concentrations in the rainfall to those in the McHenry storm-drain runoff showed that, for some compounds, rainfall contributed a substantial percentage of the concentration in the runoff; for other compounds, the concentrations in rainfall were much greater than in the runoff. For example, diazinon concentrations in rainfall were about 70 percent of the diazinon concentration in the runoff, whereas the chlorpyrifos concentration in the rain was 1.8 times greater than in the runoff. The more water-soluble pesticides—carbaryl, metolachlor, napropamide, and simazine—followed the same pattern as diazinon and had lower concentrations in rain compared to runoff. Similar to chlorpyrifos,compounds with low water solubilities and higher soil-organic carbon partition coefficients, including dacthal, pendimethalin, and trifluralin, were found to have higher concentrations in rain than in runoff water and were presumed to partition to the suspended sediments and organic matter on the ground. During the 2002–04 study period, the herbicide dacthal had the highest detection frequencies for all sample types collected from the Central Valley sites (67–100 percent). The most frequently detected compounds in the wet-deposition samples were dacthal, diazinon, chlorpyrifos, and simazine (greater than 90 percent). The median wet-deposition amounts for these compounds were 0.044 micrograms per square meter per day (μg/m 2 /day), 0.209 μg/m 2 /day, 0.079 μg/m 2 /day, and 0.172 μg/m 2 /day, respectively. For the dry-deposition samples, detection frequencies were greater than 73 percent for the compounds dacthal, metolachor, and chlorpyrifos, and median deposition amounts were an order of magnitude less than for wet deposition. The differences between wet deposition and dry deposition appeared to be closely related to the Henry’s Law (H) constant of each compound, although the mass deposited by dry deposition takes place over a much longer time frame. Pesticides detected in rainfall usually were detected in the aqueous phase of the soil-box runoff water, and the runoff concentrations were generally similar to those in the rainfall. For compounds detected in the aqueous phase and suspended-sediment samples of soil-box runoff, concentrations of pesticides in the aqueous phase generally were detected in low concentrations and had few corresponding detections in the suspended- sediment samples. Dacthal, diazinon, chlorpyrifos, and simazine were the most frequently detected pesticides (greater than 83 percent) in the aqueous-phase samples, with median concentrations of 0.010 μg/L, 0.045 μg/L, 0.016 μg/L, and 0.077 μg/L, respectively. Simazine was the most frequently detected compound in the suspended-sediment samples (69 percent), with a median concentration of 0.232 μg/L. Results for compounds detected in the surficial-soil samples collected throughout the study period showed that there was an increase in concentration for some compounds, indicating atmospheric deposition of these compounds onto the soil-box surface. In the San Joaquin Valley, the compounds chlorpyrifos, dacthal, and iprodione were detected at higher concentrations (between 1.4 and 2 times greater) than were found in the background samples collected from the San Joaquin Valley soil-box sites. In the Sacramento Valley, the compounds chlorpyrifos, dacthal, iprodione, parathionmethyl, and its oxygen analog, paraoxon-methyl, were detected in samples collected during the study period in low concentrations, but were not detected in the background concentration of the Sacramento Valley soil mix.

California

External quality assurance project report for the National Atmospheric Deposition Program’s National Trends Network and Mercury Deposition Network, 2013–14

The U.S. Geological Survey Branch of Quality Systems operated five distinct programs to provide external quality assurance monitoring for the National Atmospheric Deposition Program’s (NADP) National Trends Network and Mercury Deposition Network during 2013–14. The National Trends Network programs include (1) a field audit program to evaluate sample contamination and stability, (2) an interlaboratory comparison program to evaluate analytical laboratory performance, and (3) a colocated sampler program to evaluate bias from precipitation sampler upgrades. The Mercury Deposition Network programs include the (4) system blank program and (5) an interlaboratory comparison program. The results indicate that NADP data continue to be of sufficient quality for the analysis of spatial distributions and time trends for chemical constituents in wet deposition. The field audit program results indicate that sample contamination levels for calcium, nitrate, and sulfate continued to increase during the study period while sodium and chloride contamination decreased and magnesium, potassium, ammonium, and hydrogen-ion contamination have remained relatively constant. Analyte losses due to potential sample instability were negligible. The NADP Central Analytical Laboratory produced interlaboratory comparison results with low bias and variability compared to other domestic and international laboratories that support atmospheric deposition monitoring. Colocated sampler program results from dissimilar colocated collectors suggest that the retrofit of the National Trends Network with N-CON Systems precipitation collectors could cause shifts in NADP annual deposition (concentration multiplied by depth) values from +6.2 to +51 percent for ammonium, from +8.1 to +61 percent for nitrate, from 3.8 to 71 percent for sulfate, from –24 to +15 percent for hydrogenion deposition, and larger shifts (from –14 to +102 percent) for calcium, magnesium, sodium, potassium, and chloride. The N-CON Systems collector typically catches more precipitation than the NADP-approved Aerochem Metrics Model 301 collector, but it typically caught slightly less precipitation than the Aerochem Metrics collector at a wind-swept, high-altitude site during water year 2013. Paired, identical OTT Pluvio-2 and ETI Noah IV rain gages were operated at the same sites. Results of the colocated rain gages indicate from 0 to 3.7 percent median absolute percent difference for weekly precipitation-depth measurements and from 0.05 to 5.6 absolute percent difference for annual total precipitation depth. The Mercury Deposition Network programs include the system blank program and an interlaboratory comparison program. System blank results indicated that maximum total mercury contamination concentrations in samples were less than the third percentile of all Mercury Deposition Network sample concentrations. The Mercury Analytical Laboratory produced chemical concentration results with low bias and variability compared with other domestic and international laboratories that support atmospheric-deposition monitoring.

Scientific Investigations Report

External quality assurance project report for the National Atmospheric Deposition Program’s National Trends Network and Mercury Deposition Network, 2015–16

The U.S. Geological Survey Precipitation Chemistry Quality Assurance project operated five distinct programs to provide external quality assurance monitoring for the National Atmospheric Deposition Program’s (NADP) National Trends Network and Mercury Deposition Network during 2015–16. The National Trends Network programs include (1) a field audit program to evaluate sample contamination and stability, (2) an interlaboratory comparison program to evaluate analytical laboratory performance, and (3) a colocated sampler program to evaluate bias and variability attributed to automated precipitation samplers. The Mercury Deposition Network programs include the (4) system blank program and (5) an interlaboratory comparison program. The results indicate that NADP data continue to be of sufficient quality for the analysis of spatial distributions and time trends for chemical constituents in wet deposition. The field audit program results indicate increased sample contamination for calcium, magnesium, and potassium relative to 2010 levels, and slight fluctuation in sodium contamination. Nitrate contamination levels dropped slightly during 2014–16, and chloride contamination leveled off between 2007 and 2016. Sulfate contamination is similar to the 2000 level. Hydrogen ion contamination has steadily decreased since 2012. Losses of ammonium and nitrate resulting from potential sample instability were negligible. The NADP Central Analytical Laboratory produced interlaboratory comparison results with low bias and variability compared to other domestic and international laboratories that support atmospheric deposition monitoring. Significant absolute bias above the magnitudes of the detection limits was observed for nitrate and sulfate concentrations, but no analyte determinations exceeded the detection limits for blanks. Colocated sampler program results from dissimilar colocated collectors indicate that the retrofit of the National Trends Network with N-CON Systems Company, Inc. precipitation collectors could cause substantial shifts in NADP annual deposition (concentration multiplied by depth) values. Median weekly relative percent differences for analyte concentrations ranged from -4 to +76 percent for cations, from 5 to 6 percent for ammonium, from +14 to +25 percent for anions, and from -21 to +8 percent for hydrogen ion contamination. By comparison, weekly absolute concentration differences for paired identical N-CON Systems Company, Inc., collectors ranged from 4–22 percent for cations; 2–9 percent for anions; 4–5 percent for ammonium; and 13–14 percent for hydrogen ion contamination. The N-CON Systems Company, Inc. collector caught more precipitation than the Aerochem Metrics Model 301 collector (ACM) at the WA99/99WA sites, but it typically caught slightly less precipitation than the ACM at ND11/11ND, sites which receive more wind and snow than WA99/99WA. Paired, identical OTT Pluvio-2 and ETI Noah IV precipitation gages were operated at the same sites. Median absolute percent differences for daily measured precipitation depths ranged from 0 to 7 percent. Annual absolute differences ranged from 0.08 percent (ETI Noah IV precipitation gages) to 11 percent (OTT Pluvio-2 precipitation gages). The Mercury Deposition Network programs include the system blank program and an interlaboratory comparison program. System blank results indicate that maximum total mercury contamination concentrations in samples were less than the third percentile of all Mercury Deposition Network sample concentrations (1.098 nanograms per liter; ng/L). The Mercury Analytical Laboratory produced chemical concentration results with low bias and variability compared with other domestic and international laboratories that support atmospheric-deposition monitoring. The laboratory’s performance results indicate a +1-ng/L shift in bias between 2015 (-0.4 ng/L) and 2016 (+0.5 ng/L).

Scientific Investigations Report