{"pageNumber":"342","pageRowStart":"8525","pageSize":"25","recordCount":16445,"records":[{"id":70023706,"text":"70023706 - 2001 - Petrographic and geochemical evidence for the formation of primary, bacterially induced lacustrine dolomite: La Roda 'white earth' (Pliocene, Central Spain)","interactions":[],"lastModifiedDate":"2012-03-12T17:20:12","indexId":"70023706","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":3369,"text":"Sedimentology","active":true,"publicationSubtype":{"id":10}},"title":"Petrographic and geochemical evidence for the formation of primary, bacterially induced lacustrine dolomite: La Roda 'white earth' (Pliocene, Central Spain)","docAbstract":"Upper Pliocene dolomites ('white earth') from La Roda, Spain, offer a good opportunity to evaluate the process of dolomite formation in lakes. The relatively young nature of the deposits could allow a link between dolomites precipitated in modern lake systems and those present in older lacustrine formations. The La Roda Mg-carbonates (dolomite unit) occur as a 3??5- to 4-m- thick package of poorly indurated, white, massive dolomite beds with interbedded thin deposits of porous carbonate displaying root and desiccation traces as well as local lenticular gypsum moulds. The massive dolomite beds consist mainly of loosely packed 1- to 2-??m-sized aggregates of dolomite crystals exhibiting poorly developed faces, which usually results in a subrounded morphology of the crystals. Minute rhombs of dolomite are sparse within the aggregates. Both knobbly textures and clumps of spherical bodies covering the crystal surfaces indicate that bacteria were involved in the formation of the dolomites. In addition, aggregates of euhedral dolomite crystals are usually present in some more clayey (sepiolite) interbeds. The thin porous carbonate (mostly dolomite) beds exhibit both euhedral and subrounded, bacterially induced dolomite crystals. The carbonate is mainly Ca-dolomite (51-54 mol% CaCO3), showing a low degree of ordering (degree of ordering ranges from 0??27 to 0??48). Calcite is present as a subordinate mineral in some samples. Sr, Mn and Fe contents show very low correlation coefficients with Mg/Ca ratios, whereas SiO2 and K contents are highly correlated. ??18O- and ??13C-values in dolomites range from -3??07??? to 5??40??? PDB (mean = 0??06, ?? = 1??75) and from -6??34??? to -0??39??? PDB (mean = -3??55, ?? = 1??33) respectively. Samples containing significant amounts of both dolomite and calcite do not in general show significant enrichment or depletion in 18O and 13C between the two minerals. The correlation coefficient between ??18O and ??13C for dolomite is extremely low and negative (r = -0??05), whereas it is higher and positive (r = 0??47) for calcite. The lacustrine dolomite deposit from La Roda is interpreted mainly as a result of primary precipitation of dolomite in a shallow, hydrologically closed perennial lake. The lake was supplied by highly saturated HCO3-/CO32- groundwater that leached dolomitic Mesozoic formations. Precipitation of dolomite from alkaline lake waters took place under a semi-arid to arid climate. However, according to our isotopic data, strong evaporative conditions were not required for the formation of the La Roda dolomite. A significant contribution by bacteria to the formation of the dolomites is assumed in view of both petrographic and geochemical evidence.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Sedimentology","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1046/j.1365-3091.2001.00388.x","issn":"00370746","usgsCitation":"Garcia, D., Cura, M., Calvo, J.P., Ordonez, S., Jones, B., and Canaveras, J., 2001, Petrographic and geochemical evidence for the formation of primary, bacterially induced lacustrine dolomite: La Roda 'white earth' (Pliocene, Central Spain): Sedimentology, v. 48, no. 4, p. 897-915, https://doi.org/10.1046/j.1365-3091.2001.00388.x.","startPage":"897","endPage":"915","numberOfPages":"19","costCenters":[],"links":[{"id":478922,"rank":10000,"type":{"id":41,"text":"Open Access External Repository Page"},"url":"https://doi.org/10.1046/j.1365-3091.2001.00388.x","text":"External Repository"},{"id":207545,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1046/j.1365-3091.2001.00388.x"},{"id":232582,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"48","issue":"4","noUsgsAuthors":false,"publicationDate":"2001-12-21","publicationStatus":"PW","scienceBaseUri":"505a7791e4b0c8380cd7851a","contributors":{"authors":[{"text":"Garcia, Del","contributorId":72169,"corporation":false,"usgs":true,"family":"Garcia","given":"Del","email":"","affiliations":[],"preferred":false,"id":398508,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Cura, M.A.","contributorId":92017,"corporation":false,"usgs":true,"family":"Cura","given":"M.A.","email":"","affiliations":[],"preferred":false,"id":398509,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Calvo, J. P.","contributorId":24136,"corporation":false,"usgs":true,"family":"Calvo","given":"J.","email":"","middleInitial":"P.","affiliations":[],"preferred":false,"id":398505,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Ordonez, S.","contributorId":100156,"corporation":false,"usgs":true,"family":"Ordonez","given":"S.","email":"","affiliations":[],"preferred":false,"id":398510,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Jones, B.F.","contributorId":52156,"corporation":false,"usgs":true,"family":"Jones","given":"B.F.","email":"","affiliations":[],"preferred":false,"id":398506,"contributorType":{"id":1,"text":"Authors"},"rank":5},{"text":"Canaveras, J.C.","contributorId":66885,"corporation":false,"usgs":true,"family":"Canaveras","given":"J.C.","email":"","affiliations":[],"preferred":false,"id":398507,"contributorType":{"id":1,"text":"Authors"},"rank":6}]}}
,{"id":70023737,"text":"70023737 - 2001 - Transport and fate of organic wastes in groundwater at the Stringfellow hazardous waste disposal site, southern California","interactions":[],"lastModifiedDate":"2018-12-03T08:32:04","indexId":"70023737","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2233,"text":"Journal of Contaminant Hydrology","active":true,"publicationSubtype":{"id":10}},"title":"Transport and fate of organic wastes in groundwater at the Stringfellow hazardous waste disposal site, southern California","docAbstract":"<div id=\"abstracts\" class=\"Abstracts\"><div id=\"aep-abstract-id10\" class=\"abstract author\"><div id=\"aep-abstract-sec-id11\"><p><span>In January 1999,&nbsp;wastewater&nbsp;influent and&nbsp;effluent&nbsp;from the&nbsp;pretreatment&nbsp;plant at the Stringfellow hazardous&nbsp;waste disposal&nbsp;site were sampled along with&nbsp;groundwater&nbsp;at six locations along the groundwater contaminant&nbsp;plume. The objectives of this sampling and study were to identify at the compound class level the unidentified 40–60% of wastewater&nbsp;organic contaminants, and to determine what organic compound classes were being removed by the wastewater pretreatment plant, and what organic compound classes persisted during subsurface waste migration. The unidentified&nbsp;organic wastes&nbsp;are primarily chlorinated aromatic&nbsp;sulfonic acids&nbsp;derived from wastes from DDT manufacture. Trace amounts of&nbsp;EDTA&nbsp;and NTA organic&nbsp;complexing agents&nbsp;were discovered along with&nbsp;carboxylate&nbsp;metabolites&nbsp;of the common alkylphenolpolyethoxylate&nbsp;plasticizers&nbsp;and nonionic&nbsp;surfactants. The wastewater pretreatment plant removed most of the aromatic chlorinated sulfonic acids that have hydrophobic neutral properties, but the&nbsp;</span><i>p</i>-chlorobenzenesulfonic acid which is the primary waste constituent passed through the pretreatment plant and was discharged in the treated wastewaters transported to an industrial sewer. During migration in groundwater,<span>&nbsp;</span><i>p</i><span>-chlorobenzenesulfonic acid is removed by natural&nbsp;remediation&nbsp;processes. Wastewater organic contaminants have decreased 3- to 45-fold in the groundwater from 1985 to 1999 as a result of site remediation and natural remediation processes. The chlorinated aromatic sulfonic acids with hydrophobic neutral properties persist and have migrated into groundwater that underlies the adjacent residential community.</span></p></div></div></div>","language":"English","publisher":"Elsevier ","doi":"10.1016/S0169-7722(01)00133-4","issn":"01697722","usgsCitation":"Leenheer, J., Hsu, J., and Barber, L.B., 2001, Transport and fate of organic wastes in groundwater at the Stringfellow hazardous waste disposal site, southern California: Journal of Contaminant Hydrology, v. 51, no. 3-4, p. 163-178, https://doi.org/10.1016/S0169-7722(01)00133-4.","productDescription":"16 p.","startPage":"163","endPage":"178","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232506,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207506,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1016/S0169-7722(01)00133-4"}],"volume":"51","issue":"3-4","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505bb743e4b08c986b32715d","contributors":{"authors":[{"text":"Leenheer, J.A.","contributorId":75123,"corporation":false,"usgs":true,"family":"Leenheer","given":"J.A.","affiliations":[],"preferred":false,"id":398637,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Hsu, J.","contributorId":68925,"corporation":false,"usgs":true,"family":"Hsu","given":"J.","email":"","affiliations":[],"preferred":false,"id":398636,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Barber, L. B.","contributorId":64602,"corporation":false,"usgs":true,"family":"Barber","given":"L.","email":"","middleInitial":"B.","affiliations":[],"preferred":false,"id":398635,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023739,"text":"70023739 - 2001 - Effect of scale on the behavior of atrazine in surface waters","interactions":[],"lastModifiedDate":"2012-03-12T17:20:13","indexId":"70023739","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1565,"text":"Environmental Science & Technology","onlineIssn":"1520-5851","printIssn":"0013-936X","active":true,"publicationSubtype":{"id":10}},"title":"Effect of scale on the behavior of atrazine in surface waters","docAbstract":"Field runoff is an important transport mechanism by which agricultural pesticides, including atrazine, move into the hydrologic environment. Atrazine is chosen because it is widely used, is transported in runoff relatively easily, is widely observed in surface waters, and has relatively little loss in the stream network. Data on runoff of atrazine from experimental plot and field studies is combined with annual estimates of load in numerous streams and rivers, resulting in a data set with 408 observations that span 14 orders of magnitude in area. The load as a percent of use (LAPU) on an annual basis is the parameter that is compared among the studies. There is no difference in the mean or range of LAPU values for areas from the size of experimental field plots (???0.000023 ha) and small watersheds (<100 000 ha). The relatively invariant LAPU value observed across a large range of watershed areas implies that the characteristics of atrazine itself (application method and chemical properties) are important in determining the extent of runoff. The variable influences on the extent of runoff from individual watershed characteristics and weather events are superimposed on the relatively invariant LAPU value observed across the range of watershed areas. The results from this study establish the direct relevance for agricultural field plot studies to watershed studies across the full range of scale.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Environmental Science and Technology","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1021/es001220f","issn":"0013936X","usgsCitation":"Capel, P., and Larson, S., 2001, Effect of scale on the behavior of atrazine in surface waters: Environmental Science & Technology, v. 35, no. 4, p. 648-657, https://doi.org/10.1021/es001220f.","startPage":"648","endPage":"657","numberOfPages":"10","costCenters":[],"links":[{"id":207508,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1021/es001220f"},{"id":232508,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"35","issue":"4","noUsgsAuthors":false,"publicationDate":"2001-01-12","publicationStatus":"PW","scienceBaseUri":"505a0603e4b0c8380cd5109d","contributors":{"authors":[{"text":"Capel, P. D. 0000-0003-1620-5185","orcid":"https://orcid.org/0000-0003-1620-5185","contributorId":95498,"corporation":false,"usgs":true,"family":"Capel","given":"P. D.","affiliations":[],"preferred":false,"id":398641,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Larson, S.J.","contributorId":17641,"corporation":false,"usgs":true,"family":"Larson","given":"S.J.","email":"","affiliations":[],"preferred":false,"id":398640,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023782,"text":"70023782 - 2001 - In situ stimulation of groundwater denitrification with formate to remediate nitrate contamination","interactions":[],"lastModifiedDate":"2018-12-03T09:43:33","indexId":"70023782","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1565,"text":"Environmental Science & Technology","onlineIssn":"1520-5851","printIssn":"0013-936X","active":true,"publicationSubtype":{"id":10}},"title":"In situ stimulation of groundwater denitrification with formate to remediate nitrate contamination","docAbstract":"In situ stimulation of denitrification has been proposed as a mechanism to remediate groundwater nitrate contamination. In this study, sodium formate was added to a sand and gravel aquifer on Cape Cod, MA, to test whether formate could serve as a potential electron donor for subsurface denitrification. During 16- and 10-day trials, groundwater from an anoxic nitrate-containing zone (0.5-1.5 mM) was continuously withdrawn, amended with formate and bromide, and pumped back into the aquifer. Concentrations of groundwater constituents were monitored in multilevel samplers after up to 15 m of transport by natural gradient flow. Nitrate and formate concentrations were decreased 80-100% and 60-70%, respectively, with time and subsequent travel distance, while nitrite concentrations inversely increased. The field experiment breakthrough curves were simulated with a two-dimensional site-specific model that included transport, denitrification, and microbial growth. Initial values for model parameters were obtained from laboratory incubations with aquifer core material and then refined to fit field breakthrough curves. The model and the lab results indicated that formate-enhanced nitrite reduction was nearly 4-fold slower than nitrate reduction, but in the lab, nitrite was completely consumed with sufficient exposure time. Results of this study suggest that a long-term injection of formate is necessary to test the remediation potential of this approach for nitrate contamination and that adaptation to nitrite accumulation will be a key determinative factor.In situ stimulation of denitrification has been proposed as a mechanism to remediate groundwater nitrate contamination. In this study, sodium formate was added to a sand and gravel aquifer on Cape Cod, MA, to test whether formate could serve as a potential electron donor for subsurface denitrification. During 16- and 10-day trials, groundwater from an anoxic nitrate-containing zone (0.5-1.5 mM) was continuously withdrawn, amended with formate and bromide, and pumped back into the aquifer. Concentrations of groundwater constituents were monitored in multilevel samplers after up to 15 m of transport by natural gradient flow. Nitrate and formate concentrations were decreased 80-100% and 60-70%, respectively, with time and subsequent travel distance, while nitrite concentrations inversely increased. The field experiment breakthrough curves were simulated with a two-dimensional site-specific model that included transport, denitrification, and microbial growth. Initial values for model parameters were obtained from laboratory incubations with aquifer core material and then refined to fit field breakthrough curves. The model and the lab results indicated that formate-enhanced nitrite reduction was nearly 4-fold slower than nitrate reduction, but in the lab, nitrite was completely consumed with sufficient exposure time. Results of this study suggest that a long-term injection of formate is necessary to test the remediation potential of this approach for nitrate contamination and that adaptation to nitrite accumulation will be a key determinative factor.","language":"English","publisher":"ACS","doi":"10.1021/es001360p","issn":"0013936X","usgsCitation":"Smith, R.L., Miller, D., Brooks, M.H., Widdowson, M., and Killingstad, M., 2001, In situ stimulation of groundwater denitrification with formate to remediate nitrate contamination: Environmental Science & Technology, v. 35, no. 1, p. 196-203, https://doi.org/10.1021/es001360p.","productDescription":"8 p.","startPage":"196","endPage":"203","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232547,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207525,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1021/es001360p"}],"volume":"35","issue":"1","noUsgsAuthors":false,"publicationDate":"2000-11-29","publicationStatus":"PW","scienceBaseUri":"505a39abe4b0c8380cd619da","contributors":{"authors":[{"text":"Smith, R. L.","contributorId":93904,"corporation":false,"usgs":true,"family":"Smith","given":"R.","email":"","middleInitial":"L.","affiliations":[{"id":595,"text":"U.S. Geological Survey","active":false,"usgs":true}],"preferred":false,"id":398823,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Miller, D.N.","contributorId":36324,"corporation":false,"usgs":true,"family":"Miller","given":"D.N.","email":"","affiliations":[],"preferred":false,"id":398821,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Brooks, M. H.","contributorId":107735,"corporation":false,"usgs":true,"family":"Brooks","given":"M.","email":"","middleInitial":"H.","affiliations":[],"preferred":false,"id":398825,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Widdowson, M.A.","contributorId":46262,"corporation":false,"usgs":true,"family":"Widdowson","given":"M.A.","email":"","affiliations":[],"preferred":false,"id":398822,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Killingstad, M.W.","contributorId":105478,"corporation":false,"usgs":true,"family":"Killingstad","given":"M.W.","email":"","affiliations":[],"preferred":false,"id":398824,"contributorType":{"id":1,"text":"Authors"},"rank":5}]}}
,{"id":70023783,"text":"70023783 - 2001 - Using multiple geochemical tracers to characterize the hydrogeology of the submarine spring off Crescent Beach, Florida","interactions":[],"lastModifiedDate":"2020-10-03T16:49:35.074196","indexId":"70023783","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1213,"text":"Chemical Geology","active":true,"publicationSubtype":{"id":10}},"title":"Using multiple geochemical tracers to characterize the hydrogeology of the submarine spring off Crescent Beach, Florida","docAbstract":"<p id=\"simple-para.0080\">A spectacular submarine spring is located about 4 km east of Crescent Beach, FL, in the Atlantic Ocean. The single vent feature of Crescent Beach Spring provides a unique opportunity to examine onshore–offshore hydrogeologic processes, as well as point source submarine ground water discharge. The Floridan aquifer system in northeastern Florida consists of Tertiary interspersed limestone and dolomite strata. Impermeable beds confine the water-bearing zones under artesian pressure. Miocene and younger confining strata have been eroded away at the vent feature, enabling direct hydrologic communication of Eocene ground water with coastal bottom waters.</p><p id=\"simple-para.0085\">The spring water had a salinity of 6.02, which was immediately diluted by ambient seawater during advection/mixing. The concentration of major solutes in spring water and onshore well waters confirm a generalized easterly flow direction of artesian ground water. Nutrient concentrations were generally low in the reducing vent samples, and the majority of the total nitrogen species existed as NH<sub>3</sub>. The submarine ground water tracers, Rn-222 (1174 dpm l<sup>−1</sup>, dpm), methane (232 nM) and barium (294.5 nM) were all highly enriched in the spring water relative to ambient seawater. The concentrations of the reverse redox elements U, V and Mo were expectedly low in the submarine waters. The strontium isotope ratio of the vent water (<sup>87</sup>Sr/<sup>86</sup>Sr=0.70798) suggests that the spring water contain an integrated signature indicative of Floridan aquifer system ground water. Additional Sr isotopic ratios from a series of surficial and Lower Floridan well samples suggest dynamic ground water mixing, and do not provide clear evidence for a single hydrogeologic water source at the spring vent. In this karst-dominated aquifer, such energetic mixing at the vent feature is expected, and would be facilitated by conduit and fractured flow. Radium isotope activities were utilized to estimate flow-path trajectories and to provide information on potential travel times between an onshore well and the spring. Using either<span>&nbsp;</span><sup>223</sup>Ra and<span>&nbsp;</span><sup>224</sup>Ra or<span>&nbsp;</span><sup>228</sup>Ra, and qualifying this approach with several key assumptions, estimates of water mass travel times from an upper Floridan well in Crescent Beach to the submarine vent feature (distance=4050 m) are in the order of ∼0.01–0.1 m min<sup>−1</sup>.</p>","language":"English","publisher":"Elsevier","doi":"10.1016/S0009-2541(01)00322-9","issn":"00092541","usgsCitation":"Swarzenski, P., Reich, C., Spechler, R., Kindinger, J., and Moore, W., 2001, Using multiple geochemical tracers to characterize the hydrogeology of the submarine spring off Crescent Beach, Florida: Chemical Geology, v. 179, no. 1-4, p. 187-202, https://doi.org/10.1016/S0009-2541(01)00322-9.","productDescription":"16 p.","startPage":"187","endPage":"202","numberOfPages":"16","costCenters":[],"links":[{"id":232585,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"country":"United States","state":"Florida","otherGeospatial":"Crescent Beach","geographicExtents":"{\n  \"type\": \"FeatureCollection\",\n  \"features\": [\n    {\n      \"type\": \"Feature\",\n      \"properties\": {},\n      \"geometry\": {\n        \"type\": \"Polygon\",\n        \"coordinates\": [\n          [\n            [\n              -81.28028869628905,\n              29.74798440371394\n            ],\n            [\n              -81.23153686523438,\n              29.74798440371394\n            ],\n            [\n              -81.23153686523438,\n              29.786429141465277\n            ],\n            [\n              -81.28028869628905,\n              29.786429141465277\n            ],\n            [\n              -81.28028869628905,\n              29.74798440371394\n            ]\n          ]\n        ]\n      }\n    }\n  ]\n}","volume":"179","issue":"1-4","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505bc07be4b08c986b32a152","contributors":{"authors":[{"text":"Swarzenski, P.W. 0000-0003-0116-0578","orcid":"https://orcid.org/0000-0003-0116-0578","contributorId":29487,"corporation":false,"usgs":true,"family":"Swarzenski","given":"P.W.","affiliations":[],"preferred":false,"id":398826,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Reich, C. D. 0000-0002-2534-1456","orcid":"https://orcid.org/0000-0002-2534-1456","contributorId":36978,"corporation":false,"usgs":true,"family":"Reich","given":"C. D.","affiliations":[],"preferred":false,"id":398827,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Spechler, R. M.","contributorId":85961,"corporation":false,"usgs":true,"family":"Spechler","given":"R. M.","affiliations":[],"preferred":false,"id":398829,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Kindinger, J. L.","contributorId":38983,"corporation":false,"usgs":true,"family":"Kindinger","given":"J. L.","affiliations":[],"preferred":false,"id":398828,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Moore, W.S.","contributorId":90875,"corporation":false,"usgs":true,"family":"Moore","given":"W.S.","email":"","affiliations":[],"preferred":false,"id":398830,"contributorType":{"id":1,"text":"Authors"},"rank":5}]}}
,{"id":70023882,"text":"70023882 - 2001 - Methanogenic biodegradation of charcoal production wastes in groundwater at Kingsford, Michigan, USA","interactions":[],"lastModifiedDate":"2020-02-24T06:19:17","indexId":"70023882","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1934,"text":"IAHS-AISH Publication","active":true,"publicationSubtype":{"id":10}},"title":"Methanogenic biodegradation of charcoal production wastes in groundwater at Kingsford, Michigan, USA","docAbstract":"A house exploded in the City of Kingsford, Michigan USA. The explosion was caused by CH4 that leaked into the basement from the surrounding soil. Evidence suggests that biodegradation of products from the distillation and spillage at or near a former wood carbonization plant site was the major source of CH4 and CO2 in the groundwater system. The plant area is directly upgradient from deep groundwater, samples of which are green-yellow in colour, have a very strong odour of burnt wood, contain high concentrations of mononuclear aromatic and phenolic compounds, and extremely high concentrations of volatile fatty acids. The majority of the dissolved compounds in these groundwater samples have been shown, using laboratory microcosms, to be anaerobically biodegradable to CH4 and CO2. The biodegradable compounds, and the amounts of CH4 and CO2 produced in the microcosms, are consistent with observations from field samples.","language":"English","publisher":"IAHS-AISH Publication","issn":"01447815","usgsCitation":"Michael, G.E., Warren, E., and Westjohn, D., 2001, Methanogenic biodegradation of charcoal production wastes in groundwater at Kingsford, Michigan, USA: IAHS-AISH Publication, no. 269, p. 303-310.","productDescription":"8 p.","startPage":"303","endPage":"310","numberOfPages":"8","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":231624,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"country":"United States","state":"Michigan","county":"Dickinson 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Godsy E.","contributorId":80859,"corporation":false,"usgs":true,"family":"Michael","given":"Godsy","email":"","middleInitial":"E.","affiliations":[],"preferred":false,"id":399177,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Warren, E.","contributorId":15360,"corporation":false,"usgs":true,"family":"Warren","given":"E.","email":"","affiliations":[],"preferred":false,"id":399175,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Westjohn, D.B.","contributorId":68411,"corporation":false,"usgs":true,"family":"Westjohn","given":"D.B.","affiliations":[],"preferred":false,"id":399176,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023983,"text":"70023983 - 2001 - The behaviour of 39 pesticides in surface waters as a function of scale","interactions":[],"lastModifiedDate":"2017-01-05T11:03:32","indexId":"70023983","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"The behaviour of 39 pesticides in surface waters as a function of scale","docAbstract":"A portion of applied pesticides runs off agricultural fields and is transported through surface waters. In this study, the behaviour of 39 pesticides is examined as a function of scale across 14 orders of magnitude from the field to the ocean. Data on pesticide loads in streams from two US Geological Survey programs were combined with literature data from field and watershed studies. The annual load as percent of use (LAPU) was quantified for each of the fields and watersheds and was used as the normalization factor across watersheds and compounds. The in-stream losses of each pesticide were estimated for a model stream with a 15 day travel time (similar in characteristics to the upper Mississippi River). These estimated in-stream losses agreed well with the observed changes in apparent LAPU values as a function of watershed area. In general, herbicides applied to the soil surface had the greatest LAPU values and minimal in-stream losses. Soil-incorporated herbicides had smaller LAPU values and substantial in-stream losses. Insecticides generally had LAPU values similar to the incorporated herbicides, but had more variation in their in-stream losses. On the basis of the LAPU values of the 39 pesticides as a function of watershed area, a generalized conceptual model of the movement of pesticides from the field to the ocean is suggested. The importance of considering both field runoff and in-stream losses is discussed in relation to interpreting monitoring data and making regulatory decisions.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Hydrological Processes","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1002/hyp.212","issn":"08856087","usgsCitation":"Capel, P., Larson, S., and Winterstein, T.A., 2001, The behaviour of 39 pesticides in surface waters as a function of scale: Hydrological Processes, v. 15, no. 7, p. 1251-1269, https://doi.org/10.1002/hyp.212.","productDescription":"19 p.","startPage":"1251","endPage":"1269","costCenters":[],"links":[{"id":231902,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207182,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.212"}],"volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"505ba9e4e4b08c986b3225ad","contributors":{"authors":[{"text":"Capel, P. D. 0000-0003-1620-5185","orcid":"https://orcid.org/0000-0003-1620-5185","contributorId":95498,"corporation":false,"usgs":true,"family":"Capel","given":"P. D.","affiliations":[],"preferred":false,"id":399592,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Larson, S.J.","contributorId":17641,"corporation":false,"usgs":true,"family":"Larson","given":"S.J.","email":"","affiliations":[],"preferred":false,"id":399590,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Winterstein, T. A.","contributorId":25156,"corporation":false,"usgs":true,"family":"Winterstein","given":"T.","email":"","middleInitial":"A.","affiliations":[],"preferred":false,"id":399591,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023984,"text":"70023984 - 2001 - Evaluation of persistent hydrophobic organic compounds in the Columbia River Basin using semipermeable-membrane devices","interactions":[],"lastModifiedDate":"2012-03-12T17:20:02","indexId":"70023984","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"Evaluation of persistent hydrophobic organic compounds in the Columbia River Basin using semipermeable-membrane devices","docAbstract":"Persistent hydrophobic organic compounds are of concern in the Columbia River because they have been correlated with adverse effects on wildlife. We analysed samples from nine main-stem and six tributary sites throughout the Columbia River Basin (Washington and Oregon) for polychlorinated dibenzo-p-dioxins, dibenzofurans, polychlorinated biphenyls, organochlorine pesticides, and priority-pollutant polycyclic aromatic hydrocarbons. Because these compounds may have important biological consequences at aqueous concentrations well below the detection limits associated with conventional sampling methods, we used semipermeable-membrane devices to sample water and achieved parts-per-quintillion detection limits. All of these compound classes were prevalent within the basin, but concentrations of many analytes were highest in the vicinity of Portland-Vancouver, indicating that the Willamette subbasin-and perhaps the urban area in particular-is an important source of these compounds. Data collected during basin low-flow conditions in 1997 and again during basin high-flow conditions in 1998 indicate that in-stream processes such as dilution by relatively clean inflow, and flow through island hyporheic zones may be important mechanisms for attenuating dissolved concentrations of hydrophobic compounds.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Hydrological Processes","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1002/hyp.213","issn":"08856087","usgsCitation":"McCarthy, K.A., and Gale, R., 2001, Evaluation of persistent hydrophobic organic compounds in the Columbia River Basin using semipermeable-membrane devices: Hydrological Processes, v. 15, no. 7, p. 1271-1283, https://doi.org/10.1002/hyp.213.","startPage":"1271","endPage":"1283","numberOfPages":"13","costCenters":[],"links":[{"id":207199,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.213"},{"id":231938,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"505a0caae4b0c8380cd52c47","contributors":{"authors":[{"text":"McCarthy, K. A.","contributorId":107309,"corporation":false,"usgs":true,"family":"McCarthy","given":"K.","email":"","middleInitial":"A.","affiliations":[],"preferred":false,"id":399594,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Gale, R.W.","contributorId":81653,"corporation":false,"usgs":true,"family":"Gale","given":"R.W.","email":"","affiliations":[],"preferred":false,"id":399593,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023987,"text":"70023987 - 2001 - Distribution of oxygen-18 and deuteriun in river waters across the United States","interactions":[],"lastModifiedDate":"2018-11-30T05:24:24","indexId":"70023987","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"Distribution of oxygen-18 and deuteriun in river waters across the United States","docAbstract":"<div class=\"para\">\n<p>Reconstruction of continental palaeoclimate and palaeohydrology is currently hampered by limited information about isotopic patterns in the modern hydrologic cycle. To remedy this situation and to provide baseline data for other isotope hydrology studies, more than 4800, depth- and width-integrated, stream samples from 391 selected sites within the USGS National Stream Quality Accounting Network (NASQAN) and Hydrologic Benchmark Network (HBN) were analysed for &delta;<sup>18</sup>O and &delta;<sup>2</sup>H (<a title=\"Link to external resource: http://water.usgs.gov/pubs/ofr/ofr00-160/pdf/ofr00-160.pdf\" href=\"http://water.usgs.gov/pubs/ofr/ofr00-160/pdf/ofr00-160.pdf\">http://water.usgs.gov/pubs/ofr/ofr00-160/pdf/ofr00-160.pdf</a>). Each site was sampled bimonthly or quarterly for 2&middot;5 to 3 years between 1984 and 1987. The ability of this dataset to serve as a proxy for the isotopic composition of modern precipitation in the USA is supported by the excellent agreement between the river dataset and the isotopic compositions of adjacent precipitation monitoring sites, the strong spatial coherence of the distributions of &delta;<sup>18</sup>O and &delta;<sup>2</sup>H, the good correlations of the isotopic compositions with climatic parameters, and the good agreement between the &lsquo;national&rsquo; meteoric water line (MWL) generated from unweighted analyses of samples from the 48 contiguous states of &delta;<sup>2</sup>H=8&middot;11&delta;<sup>18</sup>O+8&middot;99 (<i>r</i><sup>2</sup>=0&middot;98) and the unweighted global MWL of sites from the Global Network for Isotopes in Precipitation (GNIP) of the International Atomic Energy Agency and the World Meteorological Organization (WMO) of &delta;<sup>2</sup>H=8&middot;17&delta;<sup>18</sup>O+10&middot;35.</p>\n</div>\n<div class=\"para\">\n<p>The national MWL is composed of water samples that arise in diverse local conditions where the local meteoric water lines (LMWLs) usually have much lower slopes. Adjacent sites often have similar LMWLs, allowing the datasets to be combined into regional MWLs. The slopes of regional MWLs probably reflect the humidity of the local air mass, which imparts a distinctive evaporative isotopic signature to rainfall and hence to stream samples. Deuterium excess values range from 6 to 15&permil; in the eastern half of the USA, along the northwest coast and on the Colorado Plateau. In the rest of the USA, these values range from &minus;2 to 6&permil;, with strong spatial correlations with regional aridity. The river samples have successfully integrated the spatial variability in the meteorological cycle and provide the best available dataset on the spatial distributions of &delta;<sup>18</sup>O and &delta;<sup>2</sup>H values of meteoric waters in the USA.</p>\n</div>","language":"English","publisher":"Wiley","doi":"10.1002/hyp.217","issn":"08856087","usgsCitation":"Kendall, C., and Coplen, T.B., 2001, Distribution of oxygen-18 and deuteriun in river waters across the United States: Hydrological Processes, v. 15, no. 7, p. 1363-1393, https://doi.org/10.1002/hyp.217.","productDescription":"31 p.","startPage":"1363","endPage":"1393","onlineOnly":"N","additionalOnlineFiles":"N","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":231977,"rank":1,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"country":"United States","geographicExtents":"{\n  \"type\": \"FeatureCollection\",\n  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       -123.31054687499999,\n              49.03786794532644\n            ]\n          ]\n        ]\n      }\n    }\n  ]\n}","volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"505a02ede4b0c8380cd50273","contributors":{"authors":[{"text":"Kendall, Carol 0000-0002-0247-3405 ckendall@usgs.gov","orcid":"https://orcid.org/0000-0002-0247-3405","contributorId":1462,"corporation":false,"usgs":true,"family":"Kendall","given":"Carol","email":"ckendall@usgs.gov","affiliations":[{"id":438,"text":"National Research Program - Western Branch","active":true,"usgs":true}],"preferred":true,"id":399606,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Coplen, Tyler B. 0000-0003-4884-6008 tbcoplen@usgs.gov","orcid":"https://orcid.org/0000-0003-4884-6008","contributorId":508,"corporation":false,"usgs":true,"family":"Coplen","given":"Tyler","email":"tbcoplen@usgs.gov","middleInitial":"B.","affiliations":[{"id":37277,"text":"WMA - Earth System Processes Division","active":true,"usgs":true},{"id":37464,"text":"WMA - Laboratory & Analytical Services Division","active":true,"usgs":true},{"id":27111,"text":"National Water Quality Program","active":true,"usgs":true},{"id":436,"text":"National Research Program - Eastern Branch","active":true,"usgs":true}],"preferred":true,"id":399605,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70024020,"text":"70024020 - 2001 - Annual suspended sediment and trace element fluxes in the Mississippi, Columbia, Colorado, and Rio Grande drainage basins","interactions":[],"lastModifiedDate":"2012-03-12T17:20:02","indexId":"70024020","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"Annual suspended sediment and trace element fluxes in the Mississippi, Columbia, Colorado, and Rio Grande drainage basins","docAbstract":"Suspended sediment, sediment-associated, total trace element, phosphorus (P), and total organic carbon (TOC) fluxes were determined for the Mississippi, Columbia, Rio Grande, and Colorado Basins for the study period (the 1996, 1997, and 1998 water years) as part of the US Geological Survey's redesigned National Stream Quality Accounting Network (NASQAN) programme. The majority (??? 70%) of Cu, Zn, Cr, Ni, Ba, P, As, Fe, Mn, and Al are transported in association with suspended sediment; Sr transport seems dominated by the dissolved phase, whereas the transport of Li and TOC seems to be divided equally between both phases. Average dissolved trace element levels are markedly lower than reported during the original NASQAN programme; this seems due to the use of 'clean' sampling, processing, and analytical techniques rather than to improvements in water quality. Partitioning between sediment and water for Ag, Pb, Cd, Cr, Co, V, Be, As, Sb, Hg, and Ti could not be estimated due to a lack of detectable dissolved concentrations in most samples. Elevated suspended sediment-associated Zn levels were detected in the Ohio River Basin and elevated Hg levels were detected in the Tennessee River, the former may affect the mainstem Mississippi River, whereas the latter probably do not. Sediment-associated concentrations of Ag, Cu, Pb, Zn, Cd, Cr, Co, Ba, Mo, Sb, Hg, and Fe are markedly elevated in the upper Columbia Basin, and appear to be detectable (Zn, Cd) as far downstream as the middle of the basin. These elevated concentrations seem to result from mining and/or mining-related activities. Consistently detectable concentrations of dissolved Se were found only in the Colorado River Basin. Calculated average annual suspended sediment fluxes at the mouths of the Mississippi and Rio Grande Basins were below, whereas those for the Columbia and Colorado Basins were above previously published annual values. Downstream suspended sediment-associated and total trace element fluxes increase in the Mississippi and Columbia Basins, whereas fluxes markedly decrease in the Colorado Basin. No consistent pattern in trace element fluxes was detected in the Rio Grande Basin.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Hydrological Processes","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1002/hyp.209","issn":"08856087","usgsCitation":"Horowitz, A.J., Elrick, K.A., and Smith, J., 2001, Annual suspended sediment and trace element fluxes in the Mississippi, Columbia, Colorado, and Rio Grande drainage basins: Hydrological Processes, v. 15, no. 7, p. 1169-1207, https://doi.org/10.1002/hyp.209.","startPage":"1169","endPage":"1207","numberOfPages":"39","costCenters":[],"links":[{"id":207169,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.209"},{"id":231868,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"5059ec3ae4b0c8380cd4913b","contributors":{"authors":[{"text":"Horowitz, A. J.","contributorId":102066,"corporation":false,"usgs":true,"family":"Horowitz","given":"A.","email":"","middleInitial":"J.","affiliations":[],"preferred":false,"id":399709,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Elrick, K. A.","contributorId":98731,"corporation":false,"usgs":true,"family":"Elrick","given":"K.","email":"","middleInitial":"A.","affiliations":[],"preferred":false,"id":399708,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Smith, J.J.","contributorId":106175,"corporation":false,"usgs":true,"family":"Smith","given":"J.J.","email":"","affiliations":[],"preferred":false,"id":399710,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70024023,"text":"70024023 - 2001 - Optimal estimation of suspended-sediment concentrations in streams","interactions":[],"lastModifiedDate":"2016-10-06T16:01:12","indexId":"70024023","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"Optimal estimation of suspended-sediment concentrations in streams","docAbstract":"Optimal estimators are developed for computation of suspended-sediment concentrations in streams. The estimators are a function of parameters, computed by use of generalized least squares, which simultaneously account for effects of streamflow, seasonal variations in average sediment concentrations, a dynamic error component, and the uncertainty in concentration measurements. The parameters are used in a Kalman filter for on-line estimation and an associated smoother for off-line estimation of suspended-sediment concentrations. The accuracies of the optimal estimators are compared with alternative time-averaging interpolators and flow-weighting regression estimators by use of long-term daily-mean suspended-sediment concentration and streamflow data from 10 sites within the United States. For sampling intervals from 3 to 48 days, the standard errors of on-line and off-line optimal estimators ranged from 52.7 to 107%, and from 39.5 to 93.0%, respectively. The corresponding standard errors of linear and cubic-spline interpolators ranged from 48.8 to 158%, and from 50.6 to 176%, respectively. The standard errors of simple and multiple regression estimators, which did not vary with the sampling interval, were 124 and 105%, respectively. Thus, the optimal off-line estimator (Kalman smoother) had the lowest error characteristics of those evaluated. Because suspended-sediment concentrations are typically measured at less than 3-day intervals, use of optimal estimators will likely result in significant improvements in the accuracy of continuous suspended-sediment concentration records. Additional research on the integration of direct suspended-sediment concentration measurements and optimal estimators applied at hourly or shorter intervals is needed.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Hydrological Processes","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1002/hyp.207","issn":"08856087","usgsCitation":"Holtschlag, D., 2001, Optimal estimation of suspended-sediment concentrations in streams: Hydrological Processes, v. 15, no. 7, p. 1133-1155, https://doi.org/10.1002/hyp.207.","startPage":"1133","endPage":"1155","numberOfPages":"23","costCenters":[{"id":382,"text":"Michigan Water Science Center","active":true,"usgs":true}],"links":[{"id":231940,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207201,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.207"}],"volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"505a6ee0e4b0c8380cd7584a","contributors":{"authors":[{"text":"Holtschlag, D. J. 0000-0001-5185-4928","orcid":"https://orcid.org/0000-0001-5185-4928","contributorId":102493,"corporation":false,"usgs":true,"family":"Holtschlag","given":"D. J.","affiliations":[],"preferred":false,"id":399716,"contributorType":{"id":1,"text":"Authors"},"rank":1}]}}
,{"id":70024050,"text":"70024050 - 2001 - Applicability of NASQAN data for ecosystem assessments on the Missouri River","interactions":[],"lastModifiedDate":"2016-10-13T11:13:20","indexId":"70024050","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"Applicability of NASQAN data for ecosystem assessments on the Missouri River","docAbstract":"The effectiveness of ecological restoration efforts on large developed rivers is often unknown because comprehensive ecological monitoring programs are often absent. Although Eulerian water-quality monitoring programs, such as the National Stream Quality Accounting Network (NASQAN) program, are more common, they are usually not designed for ecological assessment. Therefore, this paper addresses the value of NASQAN for ecological assessments on the Missouri River and identifies potential program additions and modifications to assess certain ecological changes in physical habitat, biological structure and function, and ecotoxicity. Five additional sites: The analysis of chlorophyll, mercury, ATP, potential endocrine disruptors, total trace elements, and selected total hydrophobic organics; and the hourly measurement of dissolved oxygen, turbidity, and temperature are recommended. Hourly measurements would require an entirely new operational aspect to NASQAN. However, the presence of data loggers and satellite transmitters in the gauging stations at all NASQAN sites substantially improves the feasibility of continuous water-quality monitoring. The use of semipermeable membrane devices (SPMDs) to monitor dissolved bioaccumulating organics and trace elements, identification and enumeration of zooplankton, and characterization of the bioavailability of organic matter are also recommended. The effect of biological processes on the conservative assumptions that are used in flux and source determinations of NASQAN constituents are also evaluated. Organic carbon, organic nitrogen, dissolved phosphate, and dissolved inorganic nitrogen are the NASQAN constituents most vulnerable to biological processes and thus violation of conservative assumptions.","language":"English","publisher":"Wiley","doi":"10.1002/hyp.215","issn":"08856087","usgsCitation":"Blevins, D.W., and Fairchild, J., 2001, Applicability of NASQAN data for ecosystem assessments on the Missouri River: Hydrological Processes, v. 15, no. 7, p. 1347-1362, https://doi.org/10.1002/hyp.215.","productDescription":"16 p.","startPage":"1347","endPage":"1362","numberOfPages":"16","costCenters":[{"id":192,"text":"Columbia Environmental Research Center","active":true,"usgs":true}],"links":[{"id":231714,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207093,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.215"}],"volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"5059ec81e4b0c8380cd492e9","contributors":{"authors":[{"text":"Blevins, Dale W. dblevins@usgs.gov","contributorId":2729,"corporation":false,"usgs":true,"family":"Blevins","given":"Dale","email":"dblevins@usgs.gov","middleInitial":"W.","affiliations":[],"preferred":true,"id":399808,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Fairchild, James","contributorId":147786,"corporation":false,"usgs":false,"family":"Fairchild","given":"James","affiliations":[],"preferred":false,"id":399807,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023514,"text":"70023514 - 2001 - Distribution of inorganic mercury in Sacramento River water and suspended colloidal sediment material","interactions":[],"lastModifiedDate":"2018-11-30T05:51:10","indexId":"70023514","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":887,"text":"Archives of Environmental Contamination and Toxicology","active":true,"publicationSubtype":{"id":10}},"title":"Distribution of inorganic mercury in Sacramento River water and suspended colloidal sediment material","docAbstract":"<p class=\"Para\">The concentration and distribution of inorganic Hg was measured using cold-vapor atomic fluorescence spectrometry in samples collected at selected sites on the Sacramento River from below Shasta Dam to Freeport, CA, at six separate times between 1996 and 1997. Dissolved (ultrafiltered, 0.005 μm equivalent pore size) Hg concentrations remained relatively constant throughout the system, ranging from the detection limit (&lt; 0.4 ng/L) to 2.4 ng/L. Total Hg (dissolved plus colloidal suspended sediment) concentrations ranged from the detection limit at the site below Shasta Dam in September 1996 to 81 ng/L at the Colusa site in January 1997, demonstrating that colloidal sediment plays an important role in the downriver Hg transport. Sequential extractions of colloid concentrates indicate that the greatest amount of Hg associated with sediment was found in the “residual” (mineral) phase with a significant quantity also occurring in the “oxidizable” phase. Only a minor amount of Hg was observed in the “reducible” phase. Dissolved Hg loads remained constant or increased slightly in the downstream direction through the study area, whereas the total inorganic Hg load increased significantly downstream especially in the reach of the river between Bend Bridge and Colusa. Analysis of temporal variations showed that Hg loading was positively correlated to discharge.</p>","language":"English","publisher":"Springer","doi":"10.1007/s002440010159","issn":"00904341","usgsCitation":"Roth, D., Taylor, H.E., Domagalski, J.L., Dileanis, P.D., Peart, D., Antweiler, R.C., and Alpers, C.N., 2001, Distribution of inorganic mercury in Sacramento River water and suspended colloidal sediment material: Archives of Environmental Contamination and Toxicology, v. 40, no. 2, p. 161-172, https://doi.org/10.1007/s002440010159.","productDescription":"12 p.","startPage":"161","endPage":"172","costCenters":[{"id":154,"text":"California Water Science Center","active":true,"usgs":true},{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232737,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207627,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1007/s002440010159"}],"volume":"40","issue":"2","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505a02dbe4b0c8380cd5021e","contributors":{"authors":[{"text":"Roth, D.A.","contributorId":100864,"corporation":false,"usgs":true,"family":"Roth","given":"D.A.","email":"","affiliations":[],"preferred":false,"id":397892,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Taylor, Howard E. hetaylor@usgs.gov","contributorId":1551,"corporation":false,"usgs":true,"family":"Taylor","given":"Howard","email":"hetaylor@usgs.gov","middleInitial":"E.","affiliations":[{"id":5044,"text":"National Research Program - Central Branch","active":true,"usgs":true}],"preferred":true,"id":397887,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Domagalski, Joseph L. 0000-0002-6032-757X joed@usgs.gov","orcid":"https://orcid.org/0000-0002-6032-757X","contributorId":1330,"corporation":false,"usgs":true,"family":"Domagalski","given":"Joseph","email":"joed@usgs.gov","middleInitial":"L.","affiliations":[{"id":154,"text":"California Water Science Center","active":true,"usgs":true}],"preferred":true,"id":397890,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Dileanis, Peter D. dileanis@usgs.gov","contributorId":71541,"corporation":false,"usgs":true,"family":"Dileanis","given":"Peter","email":"dileanis@usgs.gov","middleInitial":"D.","affiliations":[{"id":154,"text":"California Water Science Center","active":true,"usgs":true}],"preferred":false,"id":397891,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Peart, D.B.","contributorId":45304,"corporation":false,"usgs":true,"family":"Peart","given":"D.B.","email":"","affiliations":[],"preferred":false,"id":397888,"contributorType":{"id":1,"text":"Authors"},"rank":5},{"text":"Antweiler, Ronald C. 0000-0001-5652-6034 antweil@usgs.gov","orcid":"https://orcid.org/0000-0001-5652-6034","contributorId":1481,"corporation":false,"usgs":true,"family":"Antweiler","given":"Ronald","email":"antweil@usgs.gov","middleInitial":"C.","affiliations":[{"id":5044,"text":"National Research Program - Central Branch","active":true,"usgs":true}],"preferred":true,"id":397889,"contributorType":{"id":1,"text":"Authors"},"rank":6},{"text":"Alpers, Charles N. 0000-0001-6945-7365 cnalpers@usgs.gov","orcid":"https://orcid.org/0000-0001-6945-7365","contributorId":411,"corporation":false,"usgs":true,"family":"Alpers","given":"Charles","email":"cnalpers@usgs.gov","middleInitial":"N.","affiliations":[{"id":154,"text":"California Water Science Center","active":true,"usgs":true}],"preferred":true,"id":397893,"contributorType":{"id":1,"text":"Authors"},"rank":7}]}}
,{"id":70178174,"text":"70178174 - 2001 - Assessment of selenium effects in lotic ecosystems","interactions":[],"lastModifiedDate":"2016-11-04T13:02:32","indexId":"70178174","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1480,"text":"Ecotoxicology and Environmental Safety","active":true,"publicationSubtype":{"id":10}},"title":"Assessment of selenium effects in lotic ecosystems","docAbstract":"<p><span>The selenium literature has grown substantially in recent years to encompass new information in a variety of areas. Correspondingly, several different approaches to establishing a new water quality criterion for selenium have been proposed since establishment of the national water quality criterion in 1987. Diverging viewpoints and interpretations of the selenium literature have lead to opposing perspectives on issues such as establishing a national criterion based on a sediment-based model, using hydrologic units to set criteria for stream reaches, and applying lentic-derived effects to lotic environments. This Commentary presents information on the lotic verse lentic controversy. Recently, an article was published that concluded that no adverse effects were occurring in a cutthroat trout population in a coldwater river with elevated selenium concentrations (C. J. Kennedy, L. E. McDonald, R. Loveridge, and M. M. Strosher, 2000, </span><i>Arch. Environ. Contam. Toxicol.</i><span> 39, 46–52). This article has added to the controversy rather than provided further insight into selenium toxicology. Information, or rather missing information, in the article has been critically reviewed and problems in the interpretations are discussed.</span></p>","language":"English","publisher":"Elsevier","doi":"10.1006/eesa.2001.2111","usgsCitation":"Hamilton, S., and Palace, V.P., 2001, Assessment of selenium effects in lotic ecosystems: Ecotoxicology and Environmental Safety, v. 50, no. 3, p. 161-166, https://doi.org/10.1006/eesa.2001.2111.","productDescription":"6 p.","startPage":"161","endPage":"166","costCenters":[{"id":192,"text":"Columbia Environmental Research Center","active":true,"usgs":true}],"links":[{"id":330767,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"50","issue":"3","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"581d9e2ce4b0dee4cc90cbd1","contributors":{"authors":[{"text":"Hamilton, Steven J.","contributorId":174108,"corporation":false,"usgs":false,"family":"Hamilton","given":"Steven J.","affiliations":[],"preferred":false,"id":653135,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Palace, Vince P.","contributorId":176210,"corporation":false,"usgs":false,"family":"Palace","given":"Vince","email":"","middleInitial":"P.","affiliations":[],"preferred":false,"id":653136,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70185193,"text":"70185193 - 2001 - In situ spectroscopic and solution analyses of the reductive dissolution of Mn02 by Fe(II)","interactions":[],"lastModifiedDate":"2018-12-03T08:40:13","indexId":"70185193","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1565,"text":"Environmental Science & Technology","onlineIssn":"1520-5851","printIssn":"0013-936X","active":true,"publicationSubtype":{"id":10}},"title":"In situ spectroscopic and solution analyses of the reductive dissolution of Mn02 by Fe(II)","docAbstract":"<p><span>The reductive dissolution of MnO</span><sub>2</sub><span> by Fe(II) under conditions simulating acid mine drainage (pH 3, 100 mM SO</span><sub>4</sub><sup>2</sup><sup>-</sup><span>) was investigated by utilizing a flow-through reaction cell and synchrotron X-ray absorption spectroscopy. This configuration allows collection of in situ, real-time X-ray absorption near-edge structure (XANES) spectra and bulk solution samples. Analysis of the solution chemistry suggests that the reaction mechanism changed (decreased reaction rate) as MnO</span><sub>2</sub><span> was reduced and Fe(III) precipitated, primarily as ferrihydrite. Simultaneously, we observed an additional phase, with the local structure of jacobsite (MnFe</span><sub>2</sub><span>O</span><sub>4</sub><span>), in the Mn XANES spectra of reactants and products. The X-ray absorbance of this intermediate phase increased during the experiment, implying an increase in concentration. The presence of this phase, which probably formed as a surface coating, helps to explain the reduced rate of dissolution of manganese(IV) oxide. In natural environments affected by acid mine drainage, the formation of complex intermediate solid phases on mineral surfaces undergoing reductive dissolution may likewise influence the rate of release of metals to solution.</span></p>","language":"English","publisher":"American Chemical Society","doi":"10.1021/es001356d","usgsCitation":"Villinski, J.E., O’Day, P.A., Corley, T.L., and Conklin, M.H., 2001, In situ spectroscopic and solution analyses of the reductive dissolution of Mn02 by Fe(II): Environmental Science & Technology, v. 35, no. 6, p. 1157-1163, https://doi.org/10.1021/es001356d.","productDescription":"7 p. ","startPage":"1157","endPage":"1163","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":337707,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"35","issue":"6","noUsgsAuthors":false,"publicationDate":"2001-02-16","publicationStatus":"PW","scienceBaseUri":"58cba41fe4b0849ce97dc772","contributors":{"authors":[{"text":"Villinski, John E.","contributorId":189392,"corporation":false,"usgs":false,"family":"Villinski","given":"John","email":"","middleInitial":"E.","affiliations":[],"preferred":false,"id":684698,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"O’Day, Peggy A.","contributorId":189393,"corporation":false,"usgs":false,"family":"O’Day","given":"Peggy","email":"","middleInitial":"A.","affiliations":[],"preferred":false,"id":684699,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Corley, Timothy L.","contributorId":189394,"corporation":false,"usgs":false,"family":"Corley","given":"Timothy","email":"","middleInitial":"L.","affiliations":[],"preferred":false,"id":684700,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Conklin, Martha H.","contributorId":189395,"corporation":false,"usgs":false,"family":"Conklin","given":"Martha","email":"","middleInitial":"H.","affiliations":[],"preferred":false,"id":684701,"contributorType":{"id":1,"text":"Authors"},"rank":4}]}}
,{"id":70185194,"text":"70185194 - 2001 - Water sustainability -- Science or management?","interactions":[],"lastModifiedDate":"2017-03-16T10:43:59","indexId":"70185194","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":3825,"text":"Groundwater","active":true,"publicationSubtype":{"id":10}},"title":"Water sustainability -- Science or management?","docAbstract":"<p>No abstract available&nbsp;</p>","language":"English","publisher":"Wiley","doi":"10.1111/j.1745-6584.2001.tb02352.x","usgsCitation":"Wood, W., 2001, Water sustainability -- Science or management?: Groundwater, v. 39, no. 5, p. 641-641, https://doi.org/10.1111/j.1745-6584.2001.tb02352.x.","productDescription":"1 p. ","startPage":"641","endPage":"641","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":337709,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"39","issue":"5","noUsgsAuthors":false,"publicationDate":"2005-12-13","publicationStatus":"PW","scienceBaseUri":"58cba41fe4b0849ce97dc770","contributors":{"authors":[{"text":"Wood, Warren W.","contributorId":47770,"corporation":false,"usgs":false,"family":"Wood","given":"Warren W.","affiliations":[{"id":6601,"text":"Michigan State University","active":true,"usgs":false}],"preferred":false,"id":684702,"contributorType":{"id":1,"text":"Authors"},"rank":1}]}}
,{"id":70024043,"text":"70024043 - 2001 - The national stream quality accounting network: A flux-basedapproach to monitoring the water quality of large rivers","interactions":[],"lastModifiedDate":"2012-03-12T17:20:20","indexId":"70024043","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"The national stream quality accounting network: A flux-basedapproach to monitoring the water quality of large rivers","docAbstract":"Estimating the annual mass flux at a network of fixed stations is one approach to characterizing water quality of large rivers. The interpretive context provided by annual flux includes identifying source and sink areas for constituents and estimating the loadings to receiving waters, such as reservoirs or the ocean. Since 1995, the US Geological Survey's National Stream Quality Accounting Network (NASQAN) has employed this approach at a network of 39 stations in four of the largest river basins of the USA: The Mississippi, the Columbia, the Colorado and the Rio Grande. In this paper, the design of NASQAN is described and its effectiveness at characterizing the water quality of these rivers is evaluated using data from the first 3 years of operation. A broad range of constituents was measured by NASQAN, including trace organic and inorganic chemicals, major ions, sediment and nutrients. Where possible, a regression model relating concentration to discharge and season was used to interpolate between chemical observations for flux estimation. For water-quality network design, the most important finding from NASQAN was the importance of having a specific objective (that is, estimating annual mass flux) and, from that, an explicitly stated data analysis strategy, namely the use of regression models to interpolate between observations. The use of such models aided in the design of sampling strategy and provided a context for data review. The regression models essentially form null hypotheses for concentration variation that can be evaluated by the observed data. The feedback between network operation and data collection established by the hypothesis tests places the water-quality network on a firm scientific footing.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Hydrological Processes","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1002/hyp.205","issn":"08856087","usgsCitation":"Hooper, R.P., Aulenbach, B., and Kelly, V., 2001, The national stream quality accounting network: A flux-basedapproach to monitoring the water quality of large rivers: Hydrological Processes, v. 15, no. 7, p. 1089-1106, https://doi.org/10.1002/hyp.205.","startPage":"1089","endPage":"1106","numberOfPages":"18","costCenters":[],"links":[{"id":207041,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.205"},{"id":231600,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"505badfbe4b08c986b323e9c","contributors":{"authors":[{"text":"Hooper, R. P.","contributorId":26321,"corporation":false,"usgs":true,"family":"Hooper","given":"R.","email":"","middleInitial":"P.","affiliations":[],"preferred":false,"id":399785,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Aulenbach, Brent T.","contributorId":62766,"corporation":false,"usgs":true,"family":"Aulenbach","given":"Brent T.","affiliations":[],"preferred":false,"id":399786,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Kelly, V.J.","contributorId":14009,"corporation":false,"usgs":true,"family":"Kelly","given":"V.J.","email":"","affiliations":[],"preferred":false,"id":399784,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70024009,"text":"70024009 - 2001 - Chemical and isotopic evidence of nitrogen transformation in the Mississippi River, 1997-98","interactions":[],"lastModifiedDate":"2018-12-03T10:10:10","indexId":"70024009","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"Chemical and isotopic evidence of nitrogen transformation in the Mississippi River, 1997-98","docAbstract":"<p>Nitrate (NO3) and other nutrients discharged by the Mississippi River are suspected of causing a zone of depleted dissolved oxygen (hypoxic zone) in the Gulf of Mexico each summer. The hypoxic zone may have an adverse affect on aquatic life and commercial fisheries. The amount of NO3 delivered by the Mississippi River to the Gulf of Mexico is well documented, but the relative contributions of different sources of NO3, and the magnitude of subsequent in-stream transformations of NO3, are not well understood. Forty-two water samples collected in 1997 and 1998 at eight stations located either on the Mississippi River or its major tributaries were analysed for NO3, total nitrogen (N), atrazine, chloride concentrations and NO3 stable isotopes (δ15N and δ18O). These data are used to assess the magnitude and nature of in-stream N transformation and to determine if the δ15N and δ18O of NO3 provide information about NO3 sources and transformation processes in a large river system (drainage area 2 900 000 km2) that would otherwise be unavailable using concentration and discharge data alone. Results from 42 samples indicate that the δ15N and δ18O ratios between sites on the Mississippi River and its tributaries are somewhat distinctive, and vary with season and discharge rate. Of particular interest are two nearly Lagrangian sample sets, in which samples from the Mississippi River at St Francisville, LA, are compared with samples collected from the Ohio River at Grand Chain, II, and the Mississippi River at Thebes, IL. In both Lagrangian sets, mass-balance calculations indicate only a small amount of in-stream N loss. The stable isotope data from the samples suggest that in-stream N assimilation and not denitrification accounts for most of the N loss in the lower Mississippi River during the spring and early summer months.</p>","language":"English","publisher":"Wiley","doi":"10.1002/hyp.214","issn":"08856087","usgsCitation":"Battaglin, W.A., Kendall, C., Chang, C.C., Silva, S.R., and Campbell, K., 2001, Chemical and isotopic evidence of nitrogen transformation in the Mississippi River, 1997-98: Hydrological Processes, v. 15, no. 7, p. 1285-1300, https://doi.org/10.1002/hyp.214.","productDescription":"16 p.","startPage":"1285","endPage":"1300","costCenters":[{"id":191,"text":"Colorado Water Science Center","active":true,"usgs":true},{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":207092,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.214"},{"id":231711,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"country":"United States","otherGeospatial":"Mississippi River","volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"5059f546e4b0c8380cd4c14a","contributors":{"authors":[{"text":"Battaglin, William A. 0000-0001-7287-7096 wbattagl@usgs.gov","orcid":"https://orcid.org/0000-0001-7287-7096","contributorId":1527,"corporation":false,"usgs":true,"family":"Battaglin","given":"William","email":"wbattagl@usgs.gov","middleInitial":"A.","affiliations":[{"id":191,"text":"Colorado Water Science Center","active":true,"usgs":true}],"preferred":true,"id":399673,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Kendall, Carol 0000-0002-0247-3405 ckendall@usgs.gov","orcid":"https://orcid.org/0000-0002-0247-3405","contributorId":1462,"corporation":false,"usgs":true,"family":"Kendall","given":"Carol","email":"ckendall@usgs.gov","affiliations":[{"id":438,"text":"National Research Program - Western Branch","active":true,"usgs":true}],"preferred":true,"id":399675,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Chang, Cecily C.Y.","contributorId":68032,"corporation":false,"usgs":true,"family":"Chang","given":"Cecily","email":"","middleInitial":"C.Y.","affiliations":[],"preferred":false,"id":399677,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Silva, Steven R. srsilva@usgs.gov","contributorId":3162,"corporation":false,"usgs":true,"family":"Silva","given":"Steven","email":"srsilva@usgs.gov","middleInitial":"R.","affiliations":[{"id":438,"text":"National Research Program - Western Branch","active":true,"usgs":true}],"preferred":true,"id":399674,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Campbell, K.","contributorId":63351,"corporation":false,"usgs":false,"family":"Campbell","given":"K.","affiliations":[{"id":47665,"text":"St. Anthony Falls Laboratory, University of Minnesota, Minneapolis, MN, USA","active":true,"usgs":false}],"preferred":false,"id":399676,"contributorType":{"id":1,"text":"Authors"},"rank":5}]}}
,{"id":70023979,"text":"70023979 - 2001 - Estimating suspended sediment and trace element fluxes in large river basins: Methodological considerations as applied to the NASQAN programme","interactions":[],"lastModifiedDate":"2012-03-12T17:20:02","indexId":"70023979","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1924,"text":"Hydrological Processes","active":true,"publicationSubtype":{"id":10}},"title":"Estimating suspended sediment and trace element fluxes in large river basins: Methodological considerations as applied to the NASQAN programme","docAbstract":"In 1994, the NASQAN (National Stream Quality Accounting Network) programme was redesigned as a flux-based water-quality monitoring network for the Mississippi, Columbia, Colorado, and Rio Grande Basins. As the new programme represented a departure from the original, new sampling, processing, analytical, and data handling procedures had to be selected/developed to provide data on discharge, suspended sediment concentration, and the concentrations of suspended sediment and dissolved trace elements. Annual suspended sediment fluxes were estimated by summing daily instantaneous fluxes based on predicted suspended sediment concentrations derived from discharge-based log-log regression (rating-curve) models. The models were developed using both historical and current site-specific discharge and suspended sediment concentrations. Errors using this approach typically are less than ?? 10% for the 3-year reporting period; however, the magnitude of the errors increases substantially for temporal spans shorter than 1 year. Total, rather than total-recoverable, suspended sediment-associated trace element concentrations were determined by direct analysis of material dewatered from large-volume whole-water samples. Site-specific intra- and inter-annual suspended sediment-associated chemical variations were less (typically by no more than a factor of two) than those for either discharge or suspended sediment concentrations (usually more than 10-fold). The concentrations, hence the annual fluxes, for suspended sediment-associated phosphorus and organic carbon, determined by direct analyses, were higher than those determined using a more traditional paired, whole-water/filtered-water approach (by factors ranging from 1.5- to 10-fold). This may be important for such issues as eutrophication and coastal productivity. Filtered water-associated (dissolved) trace element concentrations were markedly lower than those determined during the historical NASQAN programme; many were below their respective detection limits. This resulted from the use of clean sampling, processing, and analytical protocols. Hence, the fluxes for filtered water-associated (dissolved) Ag, Pb, Co, V, Be, Sb, and Se, as well as the total (filtered water plus suspended sediment-associated) fluxes for these constituents, could not be estimated.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Hydrological Processes","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1002/hyp.206","issn":"08856087","usgsCitation":"Horowitz, A.J., Elrick, K.A., and Smith, J., 2001, Estimating suspended sediment and trace element fluxes in large river basins: Methodological considerations as applied to the NASQAN programme: Hydrological Processes, v. 15, no. 7, p. 1107-1132, https://doi.org/10.1002/hyp.206.","startPage":"1107","endPage":"1132","numberOfPages":"26","costCenters":[],"links":[{"id":207166,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.206"},{"id":231865,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"15","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"505a0b4fe4b0c8380cd52684","contributors":{"authors":[{"text":"Horowitz, A. J.","contributorId":102066,"corporation":false,"usgs":true,"family":"Horowitz","given":"A.","email":"","middleInitial":"J.","affiliations":[],"preferred":false,"id":399580,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Elrick, K. A.","contributorId":98731,"corporation":false,"usgs":true,"family":"Elrick","given":"K.","email":"","middleInitial":"A.","affiliations":[],"preferred":false,"id":399579,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Smith, J.J.","contributorId":106175,"corporation":false,"usgs":true,"family":"Smith","given":"J.J.","email":"","affiliations":[],"preferred":false,"id":399581,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023978,"text":"70023978 - 2001 - Anthropogenic organic matter in the Great Marsh of the Indiana Dunes National Lakeshore and its implications","interactions":[],"lastModifiedDate":"2012-03-12T17:20:02","indexId":"70023978","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2033,"text":"International Journal of Coal Geology","active":true,"publicationSubtype":{"id":10}},"title":"Anthropogenic organic matter in the Great Marsh of the Indiana Dunes National Lakeshore and its implications","docAbstract":"Cores from the Great Marsh area of the Indiana Dunes National Lakeshore were examined in order to document variations in concentration, type and size of anthropogenic organic matter (AnOM-coal, coke, etc.) and discuss their relationship to the concentration of such trace elements as Pb, Zn, and Mn in the near-surface sediment section. The results indicate that the first appearance of AnOM corresponds to the onset of industrialization in the area. There is also a general relationship between the occurrence of AnOM and Zn, Pb, and Mn. Trace metals were likely transported from the industrial sites to the area of their deposition as sulfur-bearing coatings on small anthropogenic particles. After deposition, these sulfur-bearing compounds reacted with organic matter within the marsh. As a result of bacterial reduction, the pyrite was produced, as suggested by a close relationship between the pyrite and AnOM. Distance from the industrial complex upwind as well as local hydrologic conditions are among the major factors controlling distribution of AnOM and trace elements. At the same distance from the source, types and sizes of AnOM are influenced by the duration and frequency of flooding. ?? 2001 Elsevier Science B.V. All rights reserved.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"International Journal of Coal Geology","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1016/S0166-5162(01)00016-7","issn":"01665162","usgsCitation":"Mastalerz, M., Souch, C., Filippelli, G.M., Dollar, N., and Perkins, S., 2001, Anthropogenic organic matter in the Great Marsh of the Indiana Dunes National Lakeshore and its implications: International Journal of Coal Geology, v. 46, no. 2-4, p. 157-177, https://doi.org/10.1016/S0166-5162(01)00016-7.","startPage":"157","endPage":"177","numberOfPages":"21","costCenters":[],"links":[{"id":231827,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207148,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1016/S0166-5162(01)00016-7"}],"volume":"46","issue":"2-4","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"5059ec5be4b0c8380cd4920e","contributors":{"authors":[{"text":"Mastalerz, Maria","contributorId":78065,"corporation":false,"usgs":true,"family":"Mastalerz","given":"Maria","affiliations":[],"preferred":false,"id":399578,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Souch, C.","contributorId":46368,"corporation":false,"usgs":true,"family":"Souch","given":"C.","email":"","affiliations":[],"preferred":false,"id":399575,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Filippelli, G. M.","contributorId":64070,"corporation":false,"usgs":false,"family":"Filippelli","given":"G.","email":"","middleInitial":"M.","affiliations":[],"preferred":false,"id":399577,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Dollar, N.L.","contributorId":24635,"corporation":false,"usgs":true,"family":"Dollar","given":"N.L.","email":"","affiliations":[],"preferred":false,"id":399574,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Perkins, S.M.","contributorId":63273,"corporation":false,"usgs":true,"family":"Perkins","given":"S.M.","email":"","affiliations":[],"preferred":false,"id":399576,"contributorType":{"id":1,"text":"Authors"},"rank":5}]}}
,{"id":70023747,"text":"70023747 - 2001 - Demonstration of significant abiotic iron isotope fractionation in nature","interactions":[],"lastModifiedDate":"2018-12-03T10:03:00","indexId":"70023747","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1796,"text":"Geology","active":true,"publicationSubtype":{"id":10}},"title":"Demonstration of significant abiotic iron isotope fractionation in nature","docAbstract":"<p><span>Field and laboratory studies reveal that the mineral ferrihydrite, formed as a result of abiotic oxidation of aqueous ferrous to ferric Fe, contains Fe that is isotopically heavy relative to coexisting aqueous Fe. Because the electron transfer step of the oxidation process at pH &gt;5 is essentially irreversible and should favor the lighter Fe isotopes in the ferric iron product, this result suggests that relatively heavy Fe isotopes are preferentially partitioned into the readily oxidized Fe(II)(OH)</span><sub><i>x</i>(aq)</sub><span>&nbsp;species or their transition complexes prior to oxidation. The apparent Fe isotope fractionation factor, α</span><sub>ferrihydrite- water</sub><span>, depends primarily on the relative abundances of the Fe(II)</span><sub>(aq)</sub><span>species. This study demonstrates that abiotic processes can fractionate the Fe isotopes to the same extent as biotic processes, and thus Fe isotopes on their own do not provide an effective biosignature.</span></p>","language":"English","publisher":"GSW","doi":"10.1130/0091-7613(2001)029<0699:DOSAII>2.0.CO;2","issn":"00917613","usgsCitation":"Bullen, T., White, A.F., Childs, C., Vivit, D., and Schultz, M., 2001, Demonstration of significant abiotic iron isotope fractionation in nature: Geology, v. 29, no. 8, p. 699-702, https://doi.org/10.1130/0091-7613(2001)029<0699:DOSAII>2.0.CO;2.","productDescription":"4 p.","startPage":"699","endPage":"702","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232667,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"29","issue":"8","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"5059fe91e4b0c8380cd4edcd","contributors":{"authors":[{"text":"Bullen, T.D.","contributorId":79911,"corporation":false,"usgs":true,"family":"Bullen","given":"T.D.","email":"","affiliations":[],"preferred":false,"id":398670,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"White, A. F.","contributorId":36546,"corporation":false,"usgs":true,"family":"White","given":"A.","email":"","middleInitial":"F.","affiliations":[],"preferred":false,"id":398668,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Childs, C.W.","contributorId":82891,"corporation":false,"usgs":true,"family":"Childs","given":"C.W.","email":"","affiliations":[],"preferred":false,"id":398671,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Vivit, D.V.","contributorId":28609,"corporation":false,"usgs":true,"family":"Vivit","given":"D.V.","email":"","affiliations":[],"preferred":false,"id":398667,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Schultz, M.S.","contributorId":66023,"corporation":false,"usgs":true,"family":"Schultz","given":"M.S.","email":"","affiliations":[],"preferred":false,"id":398669,"contributorType":{"id":1,"text":"Authors"},"rank":5}]}}
,{"id":70023721,"text":"70023721 - 2001 - Groundwater residence times in Shenandoah National Park, Blue Ridge Mountains, Virginia, USA: A multi-tracer approach","interactions":[],"lastModifiedDate":"2018-12-03T09:11:42","indexId":"70023721","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1213,"text":"Chemical Geology","active":true,"publicationSubtype":{"id":10}},"title":"Groundwater residence times in Shenandoah National Park, Blue Ridge Mountains, Virginia, USA: A multi-tracer approach","docAbstract":"<p><span>Chemical and isotopic properties of water discharging from springs and wells in Shenandoah National Park (SNP), near the crest of the Blue Ridge Mountains, VA, USA were monitored to obtain information on groundwater residence times. Investigated time scales included seasonal (wet season, April, 1996; dry season, August–September, 1997), monthly (March through September, 1999) and hourly (30-min interval recording of specific conductance and temperature, March, 1999 through February, 2000). Multiple environmental tracers, including tritium/helium-3 (</span><sup>3</sup><span>H/</span><sup>3</sup><span>He), chlorofluorocarbons (CFCs), sulfur hexafluoride (SF</span><sub>6</sub><span>), sulfur-35 (</span><sup>35</sup><span>S), and stable isotopes (</span><i>δ</i><sup>18</sup><span>O and </span><i>δ</i><sup>2</sup><span>H) of water, were used to estimate the residence times of shallow groundwater discharging from 34 springs and 15 wells. The most reliable ages of water from springs appear to be based on SF</span><sub>6</sub><span> and </span><sup>3</sup><span>H/</span><sup>3</sup><span>He, with most ages in the range of 0–3 years. This range is consistent with apparent ages estimated from concentrations of CFCs; however, CFC-based ages have large uncertainties owing to the post-1995 leveling-off of the CFC atmospheric growth curves. Somewhat higher apparent ages are indicated by </span><sup>35</sup><span>S (&gt;1.5 years) and seasonal variation of </span><i>δ</i><sup>18</sup><span>O (mean residence time of 5 years) for spring discharge. The higher ages indicated by the </span><sup>35</sup><span>S and </span><i>δ</i><sup>18</sup><span>O data reflect travel times through the unsaturated zone and, in the case of </span><sup>35</sup><span>S, possible sorption and exchange of S with soils or biomass. In springs sampled in April, 1996, apparent ages derived from the </span><sup>3</sup><span>H/</span><sup>3</sup><span>He data (median age of 0.2 years) are lower than those obtained from SF</span><sub>6</sub><span> (median age of 4.3 years), and in contrast to median ages from </span><sup>3</sup><span>H/</span><sup>3</sup><span>He (0.3 years) and SF</span><sub>6</sub><span> (0.7 years) obtained during the late summer dry season of 1997. Monthly samples from 1999 at four springs in SNP had SF</span><sub>6</sub><span>apparent ages of only 1.2 to 2.5±0.8 years, and were consistent with the 1997 SF</span><sub>6</sub><span> data. Water from springs has low excess air (0–1 cm</span><sup>3</sup><span> kg</span><sup>−1</sup><span>) and N</span><sub>2</sub><span>–Ar temperatures that vary seasonally. Concentrations of He and Ne in excess of solubility equilibrium indicate that the dissolved gases are not fractionated. The seasonal variations in N</span><sub>2</sub><span>–Ar temperatures suggest shallow, seasonal recharge, and the excess He and Ne data suggest waters mostly confined to gas exchange in the shallow, mountain-slope, water-table spring systems. Water from wells in the fractured rock contains up to 8 cm</span><sup>3</sup><span> kg</span><sup>−1</sup><span> of excess air with ages in the range of 0–25 years. Transient responses in specific conductance and temperature were observed in spring discharge within several hours of large precipitation events in September, 1999; both parameters increased initially, then decreased to values below pre-storm base-flow values. The groundwater residence times indicate that flushing rates of mobile atmospheric constituents through groundwater to streams draining the higher elevations in SNP average less than 3 years in base-flow conditions.</span></p>","language":"English","publisher":"Elsevier","doi":"10.1016/S0009-2541(01)00317-5","issn":"00092541","usgsCitation":"Plummer, N., Busenberg, E., Böhlke, J., Nelms, D., Michel, R.L., and Schlosser, P., 2001, Groundwater residence times in Shenandoah National Park, Blue Ridge Mountains, Virginia, USA: A multi-tracer approach: Chemical Geology, v. 179, no. 1-4, p. 93-111, https://doi.org/10.1016/S0009-2541(01)00317-5.","productDescription":"19 p.","startPage":"93","endPage":"111","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232187,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207329,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1016/S0009-2541(01)00317-5"}],"country":"United States","state":"Virginia","otherGeospatial":"Shenandoah National Park","volume":"179","issue":"1-4","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505a2dc0e4b0c8380cd5bff4","contributors":{"authors":[{"text":"Plummer, Niel 0000-0002-4020-1013 nplummer@usgs.gov","orcid":"https://orcid.org/0000-0002-4020-1013","contributorId":190100,"corporation":false,"usgs":true,"family":"Plummer","given":"Niel","email":"nplummer@usgs.gov","affiliations":[{"id":436,"text":"National Research Program - Eastern Branch","active":true,"usgs":true}],"preferred":true,"id":398556,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Busenberg, E.","contributorId":56796,"corporation":false,"usgs":true,"family":"Busenberg","given":"E.","affiliations":[],"preferred":false,"id":398555,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Böhlke, J.K. 0000-0001-5693-6455","orcid":"https://orcid.org/0000-0001-5693-6455","contributorId":96696,"corporation":false,"usgs":true,"family":"Böhlke","given":"J.K.","affiliations":[],"preferred":false,"id":398558,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Nelms, D.L.","contributorId":32189,"corporation":false,"usgs":true,"family":"Nelms","given":"D.L.","email":"","affiliations":[],"preferred":false,"id":398554,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Michel, R. L.","contributorId":86375,"corporation":false,"usgs":true,"family":"Michel","given":"R.","email":"","middleInitial":"L.","affiliations":[],"preferred":false,"id":398557,"contributorType":{"id":1,"text":"Authors"},"rank":5},{"text":"Schlosser, P.","contributorId":106656,"corporation":false,"usgs":true,"family":"Schlosser","given":"P.","email":"","affiliations":[],"preferred":false,"id":398559,"contributorType":{"id":1,"text":"Authors"},"rank":6}]}}
,{"id":70023720,"text":"70023720 - 2001 - Compound-specific carbon isotope analysis of a contaminant plume in Kingsford, Michigan, USA","interactions":[],"lastModifiedDate":"2020-02-24T06:20:32","indexId":"70023720","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1934,"text":"IAHS-AISH Publication","active":true,"publicationSubtype":{"id":10}},"title":"Compound-specific carbon isotope analysis of a contaminant plume in Kingsford, Michigan, USA","docAbstract":"<p>Compound-specific isotope analysis was used to study a contaminated site near Kingsford, Michigan, USA. Organic compounds at three of the sites studied had similar 13C values indicating that the contaminant source is the same for all sites. At a fourth site, chemical and 13C values had evolved due to microbial degradation of organics, with the 13C being much heavier than the starting materials. A microcosm experiment was run to observe isotopic changes with time in the methane evolved and in compounds remaining in the water during degradation. The 13C values of the methane became heavier during the initial period of the run when volatile fatty acids were being consumed. There was an abrupt decrease in the 13C values when fatty acids had been consumed and phenols began to be utilized. The 13C value of the propionate remaining in solution also increased, similar to the results found in the field.</p>","language":"English","publisher":"IAHS-AISH Publication","issn":"01447815","usgsCitation":"Michel, R.L., Silva, S.R., Bemis, B., Godsy, E., and Warren, E., 2001, Compound-specific carbon isotope analysis of a contaminant plume in Kingsford, Michigan, USA: IAHS-AISH Publication, no. 269, p. 311-316.","productDescription":"6 p.","startPage":"311","endPage":"316","numberOfPages":"6","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232186,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"country":"United States","state":"Michigan","city":"Kingsford","geographicExtents":"{\"type\":\"FeatureCollection\",\"features\":[{\"type\":\"Feature\",\"geometry\":{\"type\":\"Polygon\",\"coordinates\":[[[-87.6203,45.9852],[-87.6208,45.8973],[-87.6993,45.8976],[-87.6994,45.7219],[-87.8187,45.7217],[-87.8468,45.7218],[-87.8475,45.7218],[-87.8495,45.724],[-87.8527,45.7259],[-87.8566,45.7278],[-87.8593,45.7304],[-87.8621,45.7331],[-87.8635,45.7365],[-87.8642,45.7397],[-87.8654,45.7427],[-87.8665,45.7458],[-87.8691,45.7485],[-87.873,45.7508],[-87.8775,45.7536],[-87.8814,45.7545],[-87.8853,45.7549],[-87.8877,45.7551],[-87.8892,45.7551],[-87.8925,45.7543],[-87.8957,45.7539],[-87.899,45.7543],[-87.9016,45.7552],[-87.9056,45.7574],[-87.9076,45.758],[-87.9087,45.7581],[-87.9121,45.7577],[-87.9146,45.7582],[-87.9151,45.7583],[-87.9173,45.7587],[-87.9199,45.7586],[-87.9219,45.7573],[-87.9232,45.7569],[-87.9258,45.7574],[-87.9284,45.7581],[-87.9324,45.7593],[-87.9356,45.7598],[-87.9415,45.7584],[-87.9472,45.7581],[-87.9545,45.7587],[-87.9591,45.7588],[-87.9641,45.7601],[-87.9673,45.7615],[-87.9705,45.7633],[-87.9725,45.7644],[-87.9757,45.7663],[-87.9796,45.7676],[-87.9841,45.7695],[-87.9874,45.7705],[-87.9908,45.772],[-87.9919,45.7732],[-87.9905,45.7755],[-87.9892,45.7764],[-87.9879,45.7773],[-87.9858,45.7796],[-87.9845,45.7823],[-87.9858,45.7845],[-87.9872,45.7881],[-87.9885,45.7903],[-87.9901,45.7924],[-87.994,45.7952],[-87.9971,45.7967],[-87.9984,45.7964],[-87.9991,45.7962],[-88.0031,45.7953],[-88.0064,45.7931],[-88.0084,45.7926],[-88.0104,45.7922],[-88.014,45.791],[-88.0199,45.79],[-88.0264,45.789],[-88.0296,45.7886],[-88.0313,45.7883],[-88.0333,45.7879],[-88.0392,45.7866],[-88.0439,45.7847],[-88.0497,45.7833],[-88.0509,45.783],[-88.0549,45.7819],[-88.0583,45.7818],[-88.0595,45.7818],[-88.0641,45.7809],[-88.0694,45.7814],[-88.071,45.7818],[-88.0732,45.7826],[-88.0779,45.7848],[-88.0805,45.7861],[-88.0862,45.788],[-88.0908,45.789],[-88.095,45.7905],[-88.0989,45.7914],[-88.103,45.7937],[-88.1064,45.7966],[-88.1082,45.7991],[-88.1109,45.8013],[-88.1155,45.8035],[-88.1201,45.8053],[-88.1237,45.8067],[-88.1275,45.8086],[-88.1283,45.8092],[-88.1314,45.8118],[-88.1341,45.8143],[-88.1359,45.8164],[-88.1365,45.8196],[-88.1349,45.8225],[-88.1323,45.8249],[-88.1298,45.8273],[-88.1265,45.8296],[-88.1195,45.8342],[-88.1159,45.8368],[-88.1154,45.8371],[-88.1124,45.8388],[-88.1093,45.8408],[-88.1079,45.8431],[-88.1059,45.8454],[-88.1042,45.8472],[-88.1025,45.8486],[-88.101,45.8499],[-88.0984,45.8523],[-88.0951,45.8541],[-88.0926,45.8562],[-88.0899,45.8584],[-88.0873,45.8603],[-88.0853,45.8626],[-88.0817,45.8644],[-88.0772,45.8658],[-88.074,45.869],[-88.0733,45.8713],[-88.0728,45.8721],[-88.0748,45.8735],[-88.0774,45.8749],[-88.0807,45.8768],[-88.085,45.8777],[-88.0882,45.879],[-88.089,45.8792],[-88.0925,45.8802],[-88.0965,45.882],[-88.1005,45.8838],[-88.1018,45.8865],[-88.1037,45.8893],[-88.1042,45.8906],[-88.1046,45.8925],[-88.1061,45.8985],[-88.1055,45.9016],[-88.1053,45.9044],[-88.104,45.9067],[-88.1036,45.9071],[-88.103,45.9076],[-88.1005,45.9099],[-88.0992,45.9117],[-88.0965,45.9131],[-88.0954,45.9141],[-88.096,45.9154],[-88.098,45.9168],[-88.1013,45.9182],[-88.1046,45.9196],[-88.1085,45.9203],[-88.1125,45.9216],[-88.1149,45.9221],[-88.1171,45.9225],[-88.1187,46.1216],[-88.1178,46.2471],[-87.7424,46.2469],[-87.6189,46.2476],[-87.6187,46.1582],[-87.6205,46.0712],[-87.6203,45.9852]]]},\"properties\":{\"name\":\"Dickinson\",\"state\":\"MI\"}}]}","issue":"269","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"5059f93ee4b0c8380cd4d50b","contributors":{"authors":[{"text":"Michel, R. L.","contributorId":86375,"corporation":false,"usgs":true,"family":"Michel","given":"R.","email":"","middleInitial":"L.","affiliations":[],"preferred":false,"id":398553,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Silva, S. R.","contributorId":27474,"corporation":false,"usgs":true,"family":"Silva","given":"S.","email":"","middleInitial":"R.","affiliations":[],"preferred":false,"id":398550,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Bemis, B.","contributorId":55608,"corporation":false,"usgs":true,"family":"Bemis","given":"B.","affiliations":[],"preferred":false,"id":398551,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Godsy, E.M.","contributorId":56685,"corporation":false,"usgs":true,"family":"Godsy","given":"E.M.","email":"","affiliations":[],"preferred":false,"id":398552,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Warren, E.","contributorId":15360,"corporation":false,"usgs":true,"family":"Warren","given":"E.","email":"","affiliations":[],"preferred":false,"id":398549,"contributorType":{"id":1,"text":"Authors"},"rank":5}]}}
,{"id":70023718,"text":"70023718 - 2001 - Effect of natural gas exsolution on specific storage in a confined aquifer undergoing water level decline","interactions":[],"lastModifiedDate":"2022-10-17T15:34:57.210806","indexId":"70023718","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1861,"text":"Ground Water","active":true,"publicationSubtype":{"id":10}},"title":"Effect of natural gas exsolution on specific storage in a confined aquifer undergoing water level decline","docAbstract":"<p>The specific storage of a porous medium, a function of the compressibility of the aquifer material and the fluid within it, is essentially constant under normal hydrologic conditions. Gases dissolved in ground water can increase the effective specific storage of a confined aquifer, however, during water level declines. This causes a reduction in pore pressure that lowers the gas solubility and results in exsolution. The exsolved gas then displaces water from storage, and the specific storage increases because gas compressibility is typically much greater than that of water or aquifer material.</p><p>This work describes the effective specific storage of a confined aquifer exsolving dissolved gas as a function of hydraulic head and the dimensionless Henry's law constant for the gas. This relation is applied in a transient simulation of ground water discharge from a confined aquifer system to a collapsed salt mine in the Genesee Valley in western New York. Results indicate that exsolution of gas significantly increased the effective specific storage in the aquifer system, thereby decreasing the water level drawdown.</p>","language":"English","publisher":"National Groundwater Association","doi":"10.1111/j.1745-6584.2001.tb02340.x","issn":"0017467X","usgsCitation":"Yager, R.M., and Fountain, J., 2001, Effect of natural gas exsolution on specific storage in a confined aquifer undergoing water level decline: Ground Water, v. 39, no. 4, p. 517-525, https://doi.org/10.1111/j.1745-6584.2001.tb02340.x.","productDescription":"9 p.","startPage":"517","endPage":"525","costCenters":[],"links":[{"id":232149,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"39","issue":"4","noUsgsAuthors":false,"publicationDate":"2005-12-13","publicationStatus":"PW","scienceBaseUri":"505a05f5e4b0c8380cd5104e","contributors":{"authors":[{"text":"Yager, R. M.","contributorId":8069,"corporation":false,"usgs":true,"family":"Yager","given":"R.","email":"","middleInitial":"M.","affiliations":[],"preferred":false,"id":398545,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Fountain, J.C.","contributorId":43104,"corporation":false,"usgs":true,"family":"Fountain","given":"J.C.","email":"","affiliations":[],"preferred":false,"id":398546,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023685,"text":"70023685 - 2001 - U.S. Geological Survey programs and investigations related to soil and water conservation","interactions":[],"lastModifiedDate":"2014-08-15T11:03:13","indexId":"70023685","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2072,"text":"International Journal of Sediment Research","active":true,"publicationSubtype":{"id":10}},"title":"U.S. Geological Survey programs and investigations related to soil and water conservation","docAbstract":"The U.S. Geological Survey has a rich tradition of collecting hydrologic data, especially for fluxes of water and suspended sediment, that provide a foundation for studies of soil and water conservation. Applied and basic research has included investigations of the effects of land use on rangelands, croplands, and forests; hazards mapping; derivation of flood and drought frequency, and other statistics related to streamflow and reservoir storage; development and application of models of rainfall-runoff relations, chemical quality, and sediment movement; and studies of the interactive processes of overland and channel flow with vegetation. Networks of streamgaging stations and (or) sampling sites within numerous drainage basins are yielding information that extends databases and enhances the ability to use those data for interpretive studies.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"International Journal of Sediment Research","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","publisher":"Elsevier","issn":"10016279","usgsCitation":"Osterkamp, W.R., and Gray, J.R., 2001, U.S. Geological Survey programs and investigations related to soil and water conservation: International Journal of Sediment Research, v. 16, no. 3, p. 421-429.","productDescription":"9 p.","startPage":"421","endPage":"429","costCenters":[{"id":502,"text":"Office of Surface Water","active":true,"usgs":true}],"links":[{"id":232228,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"16","issue":"3","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505bbafee4b08c986b32843f","contributors":{"authors":[{"text":"Osterkamp, W. R.","contributorId":46044,"corporation":false,"usgs":true,"family":"Osterkamp","given":"W.","email":"","middleInitial":"R.","affiliations":[],"preferred":false,"id":398443,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Gray, J. R.","contributorId":63372,"corporation":false,"usgs":true,"family":"Gray","given":"J.","email":"","middleInitial":"R.","affiliations":[],"preferred":false,"id":398444,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
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