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USGS2014

Annual agricultural pesticide use for Midwest Stream-Quality Assessment, 2012-13

This report provides estimates of annual agricultural use of 190 pesticide compounds for counties and selected watersheds of Midwestern States for 2012 and 2013 compiled for subsequent analysis by the National Water-Quality Assessment Program, Midwest Stream-Quality Assessment (MSQA). One of the goals of MSQA is to characterize contaminants at perennial-stream sites throughout the Corn Belt. Evaluating pesticide inputs from agricultural sources will aid in that characterization. Crop acres for selected Midwestern crops were obtained from the Cropland Data Layer of the U.S. Department of Agriculture’s National Agricultural Statistics Service and used in conjunction with GfK Kynetec, Inc. proprietary Crop Reporting District-level pesticide-use data to estimate pesticide use for counties and watersheds. Estimated pesticide use (EPest) values were calculated by using both the “EPest-high” and “EPest-low” methods, the distinction being that there are more counties with estimated pesticide use for EPest-high compared to EPest-low, owing to differing assumptions about missing survey data. County-level and watershed-level estimates of annual agricultural pesticide use are provided as downloadable, tab-delimited files for both EPest-high and Epest-low. Summary graphs of MSQA watershed-level pesticide use for selected crops are also provided.

Data Series↗
USGS2014

Site-characteristic and hydrologic data for selected wells and springs on Federal land in Clark County, Nevada

Site-characteristic and hydrologic data for selected wells and springs on U.S. Bureau of Land Management, National Park Service, U.S. Fish and Wildlife Service, and U.S. Forest Service land in Clark County, Nevada, were updated in the U.S. Geological Survey’s National Water Information System (NWIS) to facilitate multi-agency research. Data were researched and reviewed, sites were visited, and NWIS data were updated for 231 wells and 198 springs, including 36 wells and 67 springs that were added to NWIS and 44 duplicate sites that were deleted. The site-characteristic and hydrologic data collected, reviewed, edited, and added to NWIS include locations, well water levels, spring discharges, and water chemistry. Site-characteristic and hydrologic data can be accessed from links to the NWIS web interface; data not available through the web interface are presented in appendixes to this report.

Nevada↗
USGS2014

Groundwater-quality data in the North San Francisco Bay Shallow Aquifer study unit, 2012: results from the California GAMA Program

Groundwater quality in the 1,850-square-mile North San Francisco Bay Shallow Aquifer (NSF-SA) study unit was investigated by the U.S. Geological Survey (USGS) from April to August 2012, as part of the California State Water Resources Control Board (SWRCB) Groundwater Ambient Monitoring and Assessment (GAMA) Program’s Priority Basin Project (PBP). The GAMA-PBP was developed in response to the California Groundwater Quality Monitoring Act of 2001 and is being conducted in collaboration with the SWRCB and Lawrence Livermore National Laboratory (LLNL). The NSF-SA study unit was the first study unit to be sampled as part of the second phase of the GAMA-PBP, which focuses on the shallow aquifer system. The GAMA NSF-SA study was designed to provide a spatially unbiased assessment of untreated-groundwater quality in the shallow aquifer systems and to facilitate statistically consistent comparisons of untreated-groundwater quality throughout California. The shallow aquifer system in the NSF-SA study unit was defined as the part of the aquifer system that is used by many private domestic wells and is shallower than the primary aquifer system used by many public-supply wells. In the NSF-SA study unit located in Marin, Mendocino, Napa, Solano, and Sonoma Counties, groundwater samples were collected from 71 wells. Seventy of the wells were selected by using a spatially distributed, randomized grid-based method to provide statistical representation of the study unit (grid wells), and one well was selected to aid in evaluation of water-quality issues (understanding well). The groundwater samples were analyzed for organic constituents (volatile organic compounds [VOCs], pesticides, and pesticide degradates); constituents of special interest (perchlorate and 1,2,3-trichloropropane [1,2,3-TCP]); naturally occurring inorganic constituents (trace elements, nutrients, major and minor ions, silica, and total dissolved solids [TDS]); and radioactive constituents (radon-222 and gross alpha and gross beta radioactivity). Naturally occurring isotopes (stable isotopes of hydrogen, oxygen, boron, strontium, and inorganic carbon in water, tritium activities, and carbon-14 abundances) were measured to help identify the sources and ages of the sampled groundwater. In total, 207 constituents and water-quality indicators were measured. Three types of quality-control samples (blanks, replicates, and matrix spikes) were collected at up to 13 percent of the wells in the NSF-SA study unit, and the results for these samples were used to evaluate the quality of the data for the groundwater samples. Blanks rarely contained detectable concentrations of any constituent, suggesting that contamination from sample-collection procedures was not a significant source of bias in the data for the groundwater samples. Replicate samples generally were within the limits of acceptable analytical reproducibility. Matrix-spike recoveries were within the acceptable range (70 to 130 percent) for approximately 91 percent of the compounds. Most of the wells sampled for this study were private domestic wells. Private domestic wells are not regulated in California, and groundwater from these wells is rarely analyzed for water-quality constituents. Although regulatory benchmarks for drinking-water quality do not apply to private domestic wells, to provide some context for the results, concentrations of constituents measured in the untreated groundwater were compared with regulatory and non-regulatory health-based benchmarks established by the U.S. Environmental Protection Agency (USEPA) and California Department of Public Health (CDPH), to non-regulatory health-based benchmarks established by the USGS in cooperation with the USEPA, and to non-regulatory benchmarks established for aesthetic concerns by the CDPH. Comparisons between data collected for this study and benchmarks for drinking water are for illustrative purposes only and are not indicative of compliance or non-compliance with those benchmarks. Most of the organic and inorganic constituents that were detected in groundwater samples from the 70 grid wells in the NSF-SA study unit were detected at concentrations less than drinking-water benchmarks. Of the 149 organic and special-interest constituents analyzed for in groundwater samples, 31 were detected; concentrations of most detected constituents were less than regulatory and non-regulatory health-based benchmarks. One VOC, benzene, and one insecticide, dieldrin, were detected at concentrations above their respective health-based benchmarks. In total, VOCs were detected in 40 percent of the grid wells sampled, pesticides and pesticide degradates were detected in 13 percent, and perchlorate was detected in 27 percent of the 70 grid wells sampled. Groundwater samples from 70 grid wells were analyzed for trace elements, major and minor ions, nutrients, and radioactive constituents; most detected concentrations were less than health-based benchmarks. Exceptions are 12 detections of manganese greater than the USGS Health-Based Screening Level (HBSL), 7 detections of arsenic greater than the USEPA maximum contaminant level (MCL-US) of 10 micrograms per liter (μg/L), 2 detections of boron greater than the HBSL of 6,000 μg/L, 2 detections of fluoride greater than the CDPH maximum contaminant level (MCL-CA) of 2 milligrams per liter (mg/L), 2 detections of nitrate greater than the MCL-US of 10 mg/L, and two detections of radon-222 greater than the proposed MCL-US of 4,000 picocuries per liter. Results for constituents with non-regulatory benchmarks set for aesthetic concerns from the grid wells showed that iron concentrations greater than the CDPH secondary maximum contaminant level (SMCL-CA) of 300 μg/L were detected in 13 grid wells. Chloride was detected at a concentration greater than the SMCL-CA recommended benchmark of 250 mg/L in two grid wells. Sulfate concentrations greater than the SMCL-CA recommended benchmark of 250 mg/L were measured in two grid wells, and the concentration in one of these wells was also greater than the SMCL-CA upper benchmark of 500 mg/L. TDS concentrations greater than the SMCL-CA recommended benchmark of 500 mg/L were measured in 15 grid wells, and concentrations in 4 of these wells were also greater than the SMCL-CA upper benchmark of 1,000 mg/L.

California↗
USGS2014

Area- and depth- weighted averages of selected SSURGO variables for the conterminous United States and District of Columbia

This digital data release consists of seven data files of soil attributes for the United States and the District of Columbia. The files are derived from National Resources Conservations Service’s (NRCS) Soil Survey Geographic database (SSURGO). The data files can be linked to the raster datasets of soil mapping unit identifiers (MUKEY) available through the NRCS’s Gridded Soil Survey Geographic (gSSURGO) database ( http://www.nrcs.usda.gov/wps/portal/nrcs/detail/soils/survey/geo/?cid=nrcs142p2_053628 ). The associated files, named DRAINAGECLASS, HYDRATING, HYDGRP, HYDRICCONDITION, LAYER, TEXT, and WTDEP are area- and depth-weighted average values for selected soil characteristics from the SSURGO database for the conterminous United States and the District of Columbia. The SSURGO tables were acquired from the NRCS on March 5, 2014. The soil characteristics in the DRAINAGE table are drainage class (DRNCLASS), which identifies the natural drainage conditions of the soil and refers to the frequency and duration of wet periods. The soil characteristics in the HYDRATING table are hydric rating (HYDRATE), a yes/no field that indicates whether or not a map unit component is classified as a "hydric soil". The soil characteristics in the HYDGRP table are the percentages for each hydrologic group per MUKEY. The soil characteristics in the HYDRICCONDITION table are hydric condition (HYDCON), which describes the natural condition of the soil component. The soil characteristics in the LAYER table are available water capacity (AVG_AWC), bulk density (AVG_BD), saturated hydraulic conductivity (AVG_KSAT), vertical saturated hydraulic conductivity (AVG_KV), soil erodibility factor (AVG_KFACT), porosity (AVG_POR), field capacity (AVG_FC), the soil fraction passing a number 4 sieve (AVG_NO4), the soil fraction passing a number 10 sieve (AVG_NO10), the soil fraction passing a number 200 sieve (AVG_NO200), and organic matter (AVG_OM). The soil characteristics in the TEXT table are percent sand, silt, and clay (AVG_SAND, AVG_SILT, and AVG_CLAY). The soil characteristics in the WTDEP table are the annual minimum water table depth (WTDEP_MIN), available water storage in the 0-25 cm soil horizon (AWS025), the minimum water table depth for the months April, May and June (WTDEPAMJ), the available water storage in the first 25 centimeters of the soil horizon (AWS25), the dominant drainage class (DRCLSD), the wettest drainage class (DRCLSWET), and the hydric classification (HYDCLASS), which is an indication of the proportion of the map unit, expressed as a class, that is "hydric", based on the hydric classification of a given MUKEY. (See Entity_Description for more detail). The tables were created with a set of arc macro language (aml) and awk (awk was created at Bell Labsin the 1970s and its name is derived from the first letters of the last names of its authors – Alfred Aho, Peter Weinberger, and Brian Kernighan) scripts. Send an email to mewieczo@usgs.gov to obtain copies of the computer code (See Process_Description.) The methods used are outlined in NRCS's "SSURGO Data Packaging and Use" (NRCS, 2011). The tables can be related or joined to the gSSURGO rasters of MUKEYs by the item 'MUKEY.' Joining or relating the tables to a MUKEY grid allows the creation of grids of area- and depth-weighted soil characteristics. A 90-meter raster of MUKEYs is provided which can be used to produce rasters of soil attributes. More detailed resolution rasters are available through NRCS via the link above.

Data Series↗
USGS2014

Characterization of selected bed-sediment-bound organic and inorganic contaminants and toxicity, Barnegat Bay and major tributaries, New Jersey, 2012

A study of bed-sediment toxicity and organic and inorganic contaminants was conducted by the U.S. Geological Survey (USGS) in cooperation with the New Jersey Department of Environmental Protection (NJDEP). Bed-sediment samples were collected once from 22 sites in Barnegat Bay and selected major tributaries during August–September 2012 and analyzed for toxicity and a suite of organic and inorganic contaminants by the USGS and the U.S. Army Corps of Engineers. Sampling sites were selected to coincide with an existing water-quality monitoring network used by the NJDEP and others in order to evaluate water-quality conditions in Barnegat Bay and the surrounding watershed. Two of the 22 sites are reference sites and are within or adjacent to the study area; bed-sediment samples from reference sites allow for comparisons of results for the Barnegat Bay watershed to results from less affected settings within the region. Toxicity testing was conducted by exposing the estuarine amphipod Leptocheirus plumulosus and the freshwater amphipod Hyalella azteca to sediments for 28 days, and the percent survival, difference in biomass, and individual dry weights were measured. Reproductive effects also were evaluated for estuarine samples. Bed-sediment samples from four sites within Barnegat Bay were subjected to a toxicity identification evaluation to determine probable causes of toxicity. Samples were analyzed for a suite of 94 currently-used pesticides, 21 legacy pesticides, 24 trace elements, 40 polycyclic aromatic hydrocarbons, 7 polychlorinated biphenyls (PCBs) as Arochlor mixtures, and 145 individual PCB congeners. Concentrations of detected compounds were compared to sediment-quality guidelines, where appropriate.

New Jersey↗
USGS2014

Watershed Data Management (WDM) database for Salt Creek streamflow simulation, DuPage County, Illinois, water years 2005-11

The U.S. Geological Survey (USGS), in cooperation with DuPage County Stormwater Management Division, maintains a USGS database of hourly meteorologic and hydrologic data for use in a near real-time streamflow simulation system, which assists in the management and operation of reservoirs and other flood-control structures in the Salt Creek watershed in DuPage County, Illinois. Most of the precipitation data are collected from a tipping-bucket rain-gage network located in and near DuPage County. The other meteorologic data (wind speed, solar radiation, air temperature, and dewpoint temperature) are collected at Argonne National Laboratory in Argonne, Ill. Potential evapotranspiration is computed from the meteorologic data. The hydrologic data (discharge and stage) are collected at USGS streamflow-gaging stations in DuPage County. These data are stored in a Watershed Data Management (WDM) database. An earlier report describes in detail the WDM database development including the processing of data from January 1, 1997, through September 30, 2004, in SEP04.WDM database. SEP04.WDM is updated with the appended data from October 1, 2004, through September 30, 2011, water years 2005–11 and renamed as SEP11.WDM. This report details the processing of meteorologic and hydrologic data in SEP11.WDM. This report provides a record of snow affected periods and the data used to fill missing-record periods for each precipitation site during water years 2005–11. The meteorologic data filling methods are described in detail in Over and others (2010), and an update is provided in this report.

Illinois↗
USGS2014

Groundwater geochemical and selected volatile organic compound data, Operable Unit 1, Naval Undersea Warfare Center, Division Keyport, Washington, July 2013

Previous investigations indicate that concentrations of chlorinated volatile organic compounds (CVOCs) are substantial in groundwater beneath the 9-acre former landfill at Operable Unit 1, Naval Undersea Warfare Center, Division Keyport, Washington. The U.S. Geological Survey has continued to monitor groundwater geochemistry to ensure that conditions remain favorable for contaminant biodegradation as specified in the Record of Decision for the site. This report presents groundwater geochemical and selected CVOC data collected at Operable Unit 1 by the U.S. Geological Survey during July 9–18, 2013, in support of longterm monitoring for natural attenuation. Groundwater samples were collected from 13 wells and 9 piezometers, as well as from 10 shallow groundwater passive-diffusion sampling sites in the nearby marsh. Samples from all wells and piezometers were analyzed for oxidation-reduction (redox) sensitive constituents and dissolved gases. Samples from all piezometers and four wells also were analyzed for CVOCs, as were all samples from the passive-diffusion sampling sites. In 2013, concentrations of redox-sensitive constituents measured at all wells and piezometers were consistent with those measured in previous years, with dissolved oxygen concentrations at all except an upgradient well 0.2 milligrams per liter or less; little to no detectable nitrate; abundant dissolved manganese, iron, and methane; and commonly detected sulfide. In the upper aquifer of the northern plantation in 2013, CVOC concentrations at all piezometers were similar to those measured in previous years, and concentrations of the reductive dechlorination byproducts ethane and ethene were slightly lower or the same as concentrations measured in 2012. In the upper aquifer of the southern plantation, CVOC concentrations measured in piezometers during 2013 continued to be variable as in previous years, and often very high, and reductive dechlorination byproducts were detected in two of the three wells and in all but one piezometer. Beneath the marsh adjacent to the southern plantation, chloroethene concentrations measured in 2013 continued to vary spatially and temporaly, and also were very high. Total CVOC concentrations, at what have been historically the most contaminated passive-diffusion sampler sites (S-4, S-4B, S-5, and S-5B) remained elevated. For the intermediate aquifer in 2013, concentrations of reductive dechlorination byproducts ethane and ethene and CVOCs were consistent with those measured in previous years.

Washington↗
USGS2014

Water-level data for the Albuquerque Basin and adjacent areas, central New Mexico, period of record through September 30, 2013

The Albuquerque Basin, located in central New Mexico, is about 100 miles long and 25–40 miles wide. The basin is defined as the extent of consolidated and unconsolidated deposits of Tertiary and Quaternary age that encompasses the structural Rio Grande Rift within the basin. Drinking-water supplies throughout the basin were obtained solely from groundwater resources until December 2008, when treatment and distribution of surface water from the Rio Grande began. A population increase of about 20 percent in the basin from 1990 to 2000 and a 22-percent increase from 2000 to 2010 resulted in an increased demand for water. An initial network of wells was established by the U.S. Geological Survey (USGS) in cooperation with the City of Albuquerque from April 1982 through September 1983 to monitor changes in groundwater levels throughout the basin. This network consisted of 6 wells with analog-to-digital recorders and 27 wells where water levels were measured monthly in 1983. Currently (2013), the network consists of 123 wells and piezometers. (A piezometer is a specialized well open to a specific depth in the aquifer, often of small diameter and nested with other piezometers open to different depths.) The USGS, in cooperation with the Albuquerque Bernalillo County Water Utility Authority, currently (2013) measures and reports water levels from the 123 wells and piezometers in the network; this report presents water-level data collected by USGS personnel at those 123 sites through water year 2013.

New Mexico↗
USGS2014

Groundwater-quality data in the Santa Cruz, San Gabriel, and Peninsular Ranges Hard Rock Aquifers study unit, 2011-2012: results from the California GAMA program

Groundwater quality in the 2,400-square-mile Santa Cruz, San Gabriel, and Peninsular Ranges Hard Rock Aquifers (Hard Rock) study unit was investigated by the U.S. Geological Survey (USGS) from March 2011 through March 2012, as part of the California State Water Resources Control Board (SWRCB) Groundwater Ambient Monitoring and Assessment (GAMA) Program’s Priority Basin Project (PBP). The GAMA-PBP was developed in response to the California Groundwater Quality Monitoring Act of 2001 and is being conducted in collaboration with the SWRCB and Lawrence Livermore National Laboratory (LLNL). The Hard Rock study unit was the 35th study unit to be sampled as part of the GAMA-PBP. The GAMA Hard Rock study was designed to provide a spatially unbiased assessment of untreated-groundwater quality in the primary aquifer system and to facilitate statistically consistent comparisons of untreated-groundwater quality throughout California. The primary aquifer system is defined as those parts of the aquifers corresponding to the perforation intervals of wells listed in the California Department of Public Health (CDPH) water-quality-monitoring database for the Hard Rock study unit. Groundwater quality in the primary aquifer system may differ from the quality in the shallower or deeper water-bearing zones; shallow groundwater may be more vulnerable to surficial contamination. In the Hard Rock study unit, groundwater samples were collected from 112 wells and springs in 3 study areas (the Santa Cruz, the San Gabriel, and the Peninsular Ranges) in San Mateo, Santa Clara, Santa Cruz, San Benito, Los Angeles, Orange, Riverside, San Bernardino, and San Diego Counties. Eighty-three wells and 11 springs were selected by using a spatially distributed, randomized grid-based method to provide statistical representation of the study unit (grid wells), and 15 wells and 3 springs were selected to aid in evaluation of water-quality issues (understanding wells). The groundwater samples were analyzed for field water-quality indicators; organic constituents; one constituent of special interest (perchlorate); naturally occurring inorganic constituents; and radioactive constituents. Naturally occurring isotopes and dissolved noble gases were also measured to help identify the sources and ages of the sampled groundwater. In total, 209 constituents and water-quality indicators were measured. Three types of quality-control samples (blanks, replicates, and matrix spikes) were collected at approximately 10 percent of the wells in the Hard Rock study unit, and the results for these samples were used to evaluate the quality of the data for the groundwater samples. Blanks rarely contained detectable concentrations of any constituent, suggesting that contamination from sample collection procedures was not a significant source of bias in the data for the groundwater samples. Replicate samples generally were within the limits of acceptable analytical reproducibility. Median matrix-spike recoveries were within the acceptable range (70 to 130 percent) for approximately 92 percent of the compounds. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, untreated groundwater typically is treated, disinfected, and (or) blended with other waters to maintain water quality. Regulatory benchmarks apply to water that is served to the consumer, not to untreated groundwater. However, to provide some context for the results, concentrations of constituents measured in the untreated groundwater were compared with regulatory and nonregulatory health-based benchmarks established by the U.S. Environmental Protection Agency (USEPA) and CDPH, and to nonregulatory benchmarks established for aesthetic concerns by the CDPH. Comparisons between data collected for this study and benchmarks for drinking water are for illustrative purposes only and are not indicative of compliance or non-compliance with those benchmarks. All organic constituents and most inorganic constituents that were detected in groundwater samples from the 112 wells in the Hard Rock study unit were detected at concentrations less than drinking-water benchmarks. Of the 149 organic and special-interest constituents, 34 were detected in groundwater samples; concentrations of all detected constituents were less than regulatory and nonregulatory health-based benchmarks. In total, VOCs were detected in 44 percent of the 94 grid wells sampled, pesticides and pesticide degradates were detected in 18 percent, and perchlorate was detected in 48 percent. Trace elements, nutrients, major and minor ions, and radioactive constituents were sampled for at 94 grid wells; most detected concentrations were less than health-based benchmarks. Exceptions in the Hard Rock study unit grid wells include 3 detections of arsenic greater than the USEPA maximum contaminant level (MCL-US) of 10 micrograms per liter (μg/L), 3 detections of boron greater than the CDPH notification level (NL-CA) of 1,000 μg/L, 2 detections of molybdenum greater than the USEPA lifetime health advisory level (HAL-US) of 40 μg/L, 2 detections of nitrite plus nitrate (as nitrogen) greater than the MCL-US of 10 milligrams per liter (mg/L), 3 detections of fluoride greater than the CDPH maximum contaminant level (MCL-CA) of 2 mg/L, 5 detections of radon-222 greater than the proposed MCL-US of 4,000 picocuries per liter (pCi/L), and 11 detections of unadjusted gross alpha radioactivity greater than the MCL-US of 15 pCi/L. Seven of the 11 samples having unadjusted gross alpha activity greater than the MCL-US also had total uranium concentrations greater than the MCL-US of 30 μg/L and (or) uranium activities greater than the MCL-CA of 20 pCi/L. Results for constituents with nonregulatory benchmarks set for aesthetic concerns showed that iron concentrations greater than the CDPH secondary maximum contaminant level (SMCL-CA) of 300 μg/L were detected in samples from 19 grid wells. Manganese concentrations greater than the SMCL-CA of 50 μg/L were detected in 27 grid wells. Chloride was detected at a concentration greater than the SMCL-CA upper benchmark of 500 mg/L in one grid well. TDS concentrations in three grid wells were greater than the SMCL-CA upper benchmark of 1,000 mg/L.

California↗
USGS2014

Geochemical and modal data for igneous rocks associated with epithermal mineral deposits

The purposes of this report are to (1) present available geochemical and modal data for igneous rocks associated with epithermal mineral deposits and (2) to make those data widely and readily available for subsequent, more in-depth consideration and interpretation. Epithermal precious and base-metal deposits are commonly associated with subduction-related calc-alkaline to alkaline arc magmatism as well as back-arc continental rift magmatism. These deposits form in association with compositionally diverse extrusive and intrusive igneous rocks. Temperature and depth regimes prevailing during deposit formation are highly variable. The deposits form from hydrothermal fluids that range from acidic to near-neutral pH, and they occur in a variety of structural settings. The disparate temperature, pressure, fluid chemistry, and structural controls have resulted in deposits with wide ranging characteristics. Economic geologists have employed these characteristics to develop classification schemes for epithermal deposits and to constrain the important genetic processes responsible for their formation.

Data Series↗
USGS2014

Dissolved pesticide concentrations entering the Sacramento-San Joaquin Delta from the Sacramento and San Joaquin Rivers, California, 2012-13

Surface-water samples were collected from the Sacramento and San Joaquin Rivers where they enter the Sacramento–San Joaquin Delta, and analyzed by the U.S. Geological Survey for a suite of 99 current-use pesticides and pesticide degradates. Samples were collected twice per month from May 2012 through July 2013 and from May 2012 through April 2013 at the Sacramento River at Freeport, and the San Joaquin River near Vernalis, respectively. Samples were analyzed by two separate laboratory methods by using gas chromatography with mass spectrometry or liquid chromatography with tandem mass spectrometry. Method detection limits ranged from 0.9 to 10.5 nanograms per liter (ng/L). A total of 37 pesticides and degradates were detected in water samples collected during the study (18 herbicides, 11 fungicides, 7 insecticides, and 1 synergist). The most frequently detected pesticides overall were the herbicide hexazinone (detected in 100 percent of the samples); 3,4-dichloroaniline (97 percent), which is a degradate of the herbicides diuron and propanil; the fungicide azoxystrobin (83 percent); and the herbicides diuron (72 percent), simazine (66 percent), and metolachlor (64 percent). Insecticides were rarely detected during the study. Pesticide concentrations varied from below the method detection limits to 984 ng/L (hexazinone). Twenty seven pesticides and (or) degradates were detected in Sacramento River samples, and the average number of pesticides per sample was six. The most frequently detected compounds in these samples were hexazinone (detected in 100 percent of samples), 3,4-dichloroaniline (97 percent), azoxystrobin (88 percent), diuron (56 percent), and simazine (50 percent). Pesticides with the highest detected maximum concentrations in Sacramento River samples included the herbicide clomazone (670 ng/L), azoxystrobin (368 ng/L), 3,4-dichloroaniline (364 ng/L), hexazinone (130 ng/L), and propanil (110 ng/L), and all but hexazinone are primarily associated with rice agriculture. In addition to the twice monthly sampling, surface-water samples were collected from the Sacramento River on 5 consecutive days following a rainfall event in the Sacramento urban area. Samples collected following this event contained an average of 11 pesticides. The insecticides carbaryl, fipronil, and imidacloprid; the herbicide DCPA; and the fungicide imazalil were only detected in the Sacramento River during this storm-runoff event, and two detections of fipronil during this period exceeded the U.S. Environmental Protection Agency Aquatic Life Benchmark (11 ng/L) for chronic toxicity to invertebrates in freshwater. In San Joaquin River samples, 26 pesticides and (or) degradates were detected, and the average number detected per sample was 9. The most frequently detected compounds in these samples were hexazinone and metolachlor (detected in 100 percent of samples); diuron (96 percent); the fungicide boscalid (96 percent); the degradates 3,4-dicloroaniline (92 percent) and NN-(3,4-Dichlorophenyl)-N’-methylurea (DCPMU; 83 percent); simazine (83 percent); and azoxystrobin (75 percent). The pesticides with the highest detected maximum concentrations were hexazinone (984 ng/L), diuron (695 ng/L), simazine (524 ng/L), the herbicide prometryn (155 ng/L), metolachlor (127 ng/L), boscalid (112 ng/L), DCPMU (111 ng/L), and the herbicide pendimethalin (108 ng/L).

California↗
USGS2015

Wetland paleoecological study of southwest coastal Louisiana: sediment cores and diatom calibration dataset

Wetland sediment data were collected in 2009 and 2010 throughout the southwest Louisiana Chenier Plain as part of a pilot study to develop a diatom-based proxy for past wetland water chemistry and the identification of sediment deposits from tropical storms. The complete dataset includes forty-six surface sediment samples and nine sediment cores. The surface sediment samples were collected in fresh, intermediate, and brackish marsh and are located coincident with Coastwide Reference Monitoring System (CRMS) sites. The nine sediment cores were collected at the Rockefeller Wildlife Refuge (RWR) located in Grand Chenier, La.

Louisiana↗
USGS2014

Pharmaceutical compounds in shallow groundwater in non-agricultural areas of Minnesota: study design, methods, and data, 2013

The U.S. Geological Survey, in cooperation with the Minnesota Pollution Control Agency, completed a study on the occurrence of pharmaceutical compounds and other contaminants of emerging concern in shallow groundwater in non-agricultural areas of Minnesota during 2013. This report describes the study design and methods for the study on the occurrence of pharmaceuticals and other contaminants of emerging concern, and presents the data collected on pharmaceutical compounds. Samples were analyzed by the U.S. Geological Survey National Water Quality Laboratory for 110 pharmaceutical compounds using research method 9017. Samples from 21 of 45 wells had detectable concentrations of at least one of the 110 compounds analyzed. One sample contained detectable concentrations of nine compounds, which was the most detected in a single sample. Fewer than five compounds were detected in most samples. Among all samples, 27 of the 110 compounds were detected in groundwater from at least one well. Desmethyldiltiazem and nicotine were the most frequently detected compounds, each detected in 5 of 46 environmental samples (one well was sampled twice so a total of 46 environmental samples were collected from 45 wells). Caffeine had the highest detectable concentration of all the compounds at 2,060 nanograms per liter.

Minnesota↗
USGS2015

Water- and air-quality and surficial bed-sediment monitoring of the Sweetwater Reservoir watershed, San Diego County, California, 2003-09

In 1998, the U.S. Geological Survey, in cooperation with the Sweetwater Authority, began a study to assess the overall health of the Sweetwater watershed in San Diego County, California. This study was designed to provide a data set that could be used to evaluate potential effects from the construction and operation of State Route 125 within the broader context of the water quality and air quality in the watershed. The study included regular sampling of water, air, and surficial bed sediment at Sweetwater Reservoir (SWR) for chemical constituents, including volatile organic compounds (VOCs), base-neutral and acid- extractable organic compounds (BNAs) that include polycyclic aromatic hydrocarbons (PAHs), pesticides, and metals. Additionally, water samples were collected for anthropogenic organic indicator compounds in and around SWR. Background water samples were collected at Loveland Reservoir for VOCs, BNAs, pesticides, and metals. Surficial bed-sediment samples were collected for PAHs, organochlorine pesticides, and metals at Sweetwater and Loveland Reservoirs. To monitor changes in contaminant concentration in water and air at SWR during the construction and operation of State Route 125, this study was divided into three phases. Phase One sampling (September 1998 to September 2004) was designed to establish baseline conditions for target compounds in terms of detection frequency and concentration in air and water. Phase Two (October 2004 to September 2007) continued sampling at selected monitoring sites during construction of State Route 125 to assess any effect from the construction process and the use of heavy equipment to build the roadway. Phase Three (October 2007 to August 2009) continued sampling for 2 years after the opening of State Route 125 to assess the potential changes in water quality related to vehicle emissions from the roadway alignment. Surficial bed-sediment samples were collected three times during the study—at the beginning of the study, at the start of Phase Two, and at the end of the study. This report describes the study design and the sampling and analytical methods and presents data from water, air, and surficial bed-sediment samples collected from the sixth to eleventh years of the study (October 2003–August 2009), spanning the last year of Phase one and all of Phases Two and Three. Data collected during the first 5 years of sampling have been previously published. Three types of quality-control samples were used in this study—matrix spikes, blanks, and replicates. Matrix-spike data are considered to be adequate if the recovery concentration is within 30 percent of the matrix concentration. Replicate data are considered to be adequate if the replicate sample concentration is within 30 percent of the environmental sample concentration. Additionally, surrogate compounds were added to most samples to monitor sample-specific performance of the analytical method. Most VOC matrix-spike recovery data associated with water samples are within acceptable criteria, but three VOCs had recoveries below the acceptable criteria; these compounds may not have been detected in water samples if they were present at low concentrations. Data for blanks associated with water samples for VOCs and metals showed no detections above their laboratory reporting levels. Most replicate data are within acceptable criteria. Quality-control data for VOC air samples resulted in flagging several reported concentrations for acetone, benzene, ethenylbenzene, and naphthalene because they may be biased high. Acetone, benzene, and toluene were detected at low concentrations in almost every VOC air blank. Some PAH and pesticide concentrations in air samples were designated as estimated because of method performance limitations. PAHs in surficial bed sediment had 83 percent of surrogates below the acceptable criteria. No matrix-spike data for metals in surficial bed sediment were outside the acceptable criteria; only beryllium had a replicate comparison outside the acceptable criteria. Sampling results show concentrations of the gasoline oxygenate methyl tert -butyl ether in water and air samples declined after it was phased out by the State of California in January 2004. The largest concentrations of gasoline hydrocarbons benzene and toluene in water were detected at or near the surface of the SWR. Isophorone and phenol were the two most frequently detected BNA compounds in water. Diuron, prometon, and simazine were the most frequently detected pesticide compounds in water. Concentrations of benzene and toluene in air samples were highest during the cooler months and had a consistent seasonal pattern over time. Ten PAH compounds were detected frequently in air samples. Twelve pesticide compounds were also detected in air samples. Surficial bed-sediment samples were analyzed for 53 PAHs; 22 of the compounds had one or more detections. Surficial bed-sediment samples were analyzed for 22 organic compounds; only 6 compounds had one or more detections. Surficial bed-sediment samples were analyzed for 37 metals.

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USGS2004

Acetamide herbicides and their degradation products in ground water and surface water of the United States, 1993-2003

During 1993 through 2003, the U.S. Geological Survey conducted a number of studies to investigate and document the occurrence, fate, and transport of acetamide herbicides and their degradation products in ground and surface water. As part of these studies, approximately 5,100 water samples were collected and analyzed for the acetamide parent herbicides acetochlor, alachlor, dimethenamid, flufenacet, and metolachlor and their degradation products ethanesulfonic acid, oxanilic acid, and sulfinyl acetic acid. During this period, various analytical methods were developed to detect and measure concentrations of acetamide herbicides and their degradation products in ground water and surface water. Results showed that the degradation products of acetamide herbicides in ground water were detected more frequently and occurred at higher concentrations than their parent compounds. Further study showed that the acetamide herbicides and their degradation products were detected more frequently in surface water than in ground water. In general, the parent compounds were detected at similar or greater frequencies than the degradation products in surface water. The developed methods and data were valuable for acquiring information about the occurrence, fate, and transport of the herbicides and their degradation products and the importance of analyzing for both parent compounds and their degradate products in water-quality studies.

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USGS2014

Data compilation for assessing sediment and toxic chemical loads from the Green River to the lower Duwamish Waterway, Washington

Between February and June 2013, the U.S. Geological Survey collected representative samples of whole water, suspended sediment, and (or) bed sediment from a single strategically located site on the Duwamish River, Washington, during seven periods of different flow conditions. Samples were analyzed by Washington-State-accredited laboratories for a large suite of compounds, including polycyclic aromatic hydrocarbons and other semivolatile compounds, polychlorinated biphenyl Aroclors and the 209 congeners, metals, dioxins/furans, volatile organic compounds, pesticides, butyltins, hexavalent chromium, and total organic carbon. Chemical concentrations associated with bulk bed sediment (<2 mm) and fine bed sediment (<62.5 μm) fractions were compared to chemical concentrations associated with suspended sediment. Bulk bed sediment concentrations generally were lower than fine bed sediment and suspended-sediment concentrations. Concurrent with the chemistry sampling, additional parameters were measured, including instantaneous river discharge, suspended-sediment concentration, sediment particle-size distribution, and general water-quality parameters. From these data, estimates of instantaneous sediment and chemical loads from the Green River to the Lower Duwamish Waterway were calculated.

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USGS2014

Evidence of Absence software

Evidence of Absence software (EoA) is a user-friendly application used for estimating bird and bat fatalities at wind farms and designing search protocols. The software is particularly useful in addressing whether the number of fatalities has exceeded a given threshold and what search parameters are needed to give assurance that thresholds were not exceeded. The software is applicable even when zero carcasses have been found in searches. Depending on the effectiveness of the searches, such an absence of evidence of mortality may or may not be strong evidence that few fatalities occurred. Under a search protocol in which carcasses are detected with nearly 100 percent certainty, finding zero carcasses would be convincing evidence that overall mortality rate was near zero. By contrast, with a less effective search protocol with low probability of detecting a carcass, finding zero carcasses does not rule out the possibility that large numbers of animals were killed but not detected in the searches. EoA uses information about the search process and scavenging rates to estimate detection probabilities to determine a maximum credible number of fatalities, even when zero or few carcasses are observed.

Data Series↗
USGS2014

Water temperature differences by plant community and location in re-established wetlands in the Sacramento-San Joaquin Delta, California, July 2005 to February 2008

Rates of carbon storage in wetlands are determined by the balance of its inputs and losses, both of which are affected by environmental factors such as water temperature and depth. In the autumn of 1997, the U.S. Geological Survey re-established two wetlands with different shallow water depths—about 25 and 55 centimeters deep—to investigate the potential to reverse subsidence of delta islands by preserving and accumulating organic substrates derived from plant biomass inputs over time. Because cooler water temperatures can slow decomposition rates and increase accretion of plant biomass, water temperature was recorded from July 2005 to February 2008 in the deeper of the two wetlands, where areas of emergent and submerged vegetation persisted throughout the study, to assess differences in water temperature between the two vegetation types. Water temperature was compared at three depths in the water column between areas of emergent and submerged vegetation and between areas near the water inflow and in the wetland interior in both vegetation types. The latter comparison was a way of evaluating the effect of the length of time water had resided in the wetland on water temperatures. There were statistically significant differences in water temperature at all depths between the two vegetation types. Overall, in areas of emergent marsh vegetation, the mean water temperature at the surface was 1.4 degrees Celsius (°C) less than it was in areas of submerged vegetation; however, when analyses accounted for the changes in temperature due to seasonal and diurnal cycles, differences in the mean water temperature between the vegetation types were even greater than this. For example, in the spring, the mean temperatures in areas of emergent marsh vegetation at the surface, mid-point, and near the sediment in the water column were 2.0, 2.3, and 2.1 °C less, respectively, than water temperatures in areas of submerged vegetation. When diurnal changes in temperature were accounted for by comparing temperatures in mid-afternoon (at 3 p.m.), water-temperature differences were even greater than the seasonal means indicated. In areas of emergent vegetation, the mean temperatures were cooler than temperatures in areas of submerged vegetation at the surface, the mid-point, and near the sediment in the water column by 3.9, 3.6, and 2.3 °C, respectively. Furthermore, from July 2005 through December 2006, water temperatures at the surface in the interior of the wetland were significantly cooler than in areas near the inflow supplying water from the San Joaquin River by 1.0 °C in areas of submerged vegetation and by 1.1 °C in areas of emergent vegetation.

California↗