{"pageNumber":"345","pageRowStart":"8600","pageSize":"25","recordCount":16506,"records":[{"id":70023609,"text":"70023609 - 2001 - Infiltration of late Palaeozoic evaporative brines in the reelfoot rift: A possible salt source for Illinois Basin formation waters and MVT mineralizing fluids","interactions":[],"lastModifiedDate":"2013-03-20T20:03:42","indexId":"70023609","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":3042,"text":"Petroleum Geoscience","active":true,"publicationSubtype":{"id":10}},"title":"Infiltration of late Palaeozoic evaporative brines in the reelfoot rift: A possible salt source for Illinois Basin formation waters and MVT mineralizing fluids","docAbstract":"Salinities and homogenization temperatures of fluid inclusions in Mississippi Valley-type (MVT) deposits provide important insights into the regional hydrology of the Illinois basin/Reelfoot rift system in late Palaeozoic time. Although the thermal regime of this basin system has been plausibly explained, the origin of high salinities in the basin fluids remains enigmatic. Topographically driven flow appears to have been essential in forming these MVT districts, as well as many other districts worldwide. However, this type of flow is recharged by fresh water making it difficult to account for the high salinities of the mineralizing fluids over extended time periods. Results of numerical experiments carried out in this study provide a possible solution to the salinity problem presented by the MVT zinc-lead and fluorite districts at the margins of the basin system. Evaporative concentration of surface water and subsequent infiltration into the subsurface are proposed to account for large volumes of brine that are ultimately responsible for mineralization of these districts. This study demonstrates that under a range of geologically reasonable conditions, brine infiltration into an aquifer in the deep subsurface can coexist with topographically driven flow. Infiltration combined with regional flow and local magmatic heat sources in the Reelfoot rift explain the brine concentrations as well as the temperatures observed in the Southern Illinois and Upper Mississippi Valley districts.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Petroleum Geoscience","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1144/petgeo.7.3.269","issn":"13540793","usgsCitation":"Rowan, E., and De Marsily, G., 2001, Infiltration of late Palaeozoic evaporative brines in the reelfoot rift: A possible salt source for Illinois Basin formation waters and MVT mineralizing fluids: Petroleum Geoscience, v. 7, no. 3, p. 269-279, https://doi.org/10.1144/petgeo.7.3.269.","startPage":"269","endPage":"279","numberOfPages":"11","costCenters":[],"links":[{"id":269822,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1144/petgeo.7.3.269"},{"id":232336,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"7","issue":"3","noUsgsAuthors":false,"publicationDate":"2022-06-06","publicationStatus":"PW","scienceBaseUri":"505a3af5e4b0c8380cd620f2","contributors":{"authors":[{"text":"Rowan, E. L. 0000-0001-5753-6189","orcid":"https://orcid.org/0000-0001-5753-6189","contributorId":34921,"corporation":false,"usgs":true,"family":"Rowan","given":"E. L.","affiliations":[],"preferred":false,"id":398196,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"De Marsily, G.","contributorId":8262,"corporation":false,"usgs":true,"family":"De Marsily","given":"G.","email":"","affiliations":[],"preferred":false,"id":398195,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023605,"text":"70023605 - 2001 - The concept of hydrologic landscapes","interactions":[],"lastModifiedDate":"2022-12-20T18:30:52.645765","indexId":"70023605","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2529,"text":"Journal of the American Water Resources Association","active":true,"publicationSubtype":{"id":10}},"title":"The concept of hydrologic landscapes","docAbstract":"Hydrologic landscapes are multiples or variations of fundamental hydrologic landscape units. A fundamental hydrologic landscape unit is defined on the basis of land-surface form, geology, and climate. The basic land-surface form of a fundamental hydrologic landscape unit is an upland separated from a lowland by an intervening steeper slope. Fundamental hydrologic landscape units have a complete hydrologic system consisting of surface runoff, ground-water flow, and interaction with atmospheric water. By describing actual landscapes in terms of land-surface slope, hydraulic properties of soils and geologic framework, and the difference between precipitation and evapotranspiration, the hydrologic system of actual landscapes can be conceptualized in a uniform way. This conceptual framework can then be the foundation for design of studies and data networks, syntheses of information on local to national scales, and comparison of process research across small study units in a variety of settings. The Crow Wing River watershed in central Minnesota is used as an example of evaluating stream discharge in the context of hydrologic landscapes. Lake-research watersheds in Wisconsin, Minnesota, North Dakota, and Nebraska are used as an example of using the hydrologic-landscapes concept to evaluate the effect of ground water on the degree of mineralization and major-ion chemistry of lakes that lie within ground-water flow systems.","language":"English","publisher":"American Water Resources Association","doi":"10.1111/j.1752-1688.2001.tb00973.x","issn":"1093474X","usgsCitation":"Winter, T.C., 2001, The concept of hydrologic landscapes: Journal of the American Water Resources Association, v. 37, no. 2, p. 335-349, https://doi.org/10.1111/j.1752-1688.2001.tb00973.x.","productDescription":"15 p.","startPage":"335","endPage":"349","costCenters":[],"links":[{"id":232260,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"country":"United States","state":"Minnesota, Nebraska, North Dakota, Wisconsin","geographicExtents":"{\"type\":\"FeatureCollection\",\"features\":[{\"type\":\"Feature\",\"geometry\":{\"type\":\"MultiPolygon\",\"coordinates\":[[[[-91.217706,43.50055],[-96.453049,43.500415],[-96.452948,45.268925],[-96.835451,45.586129],[-96.587093,45.816445],[-96.639066,45.935318],[-104.045443,45.94531],[-104.048807,48.933636],[-95.153711,48.998903],[-95.153314,49.384358],[-94.878454,49.333193],[-94.640803,48.741171],[-93.818375,48.534442],[-92.984963,48.623731],[-92.634931,48.542873],[-92.698824,48.494892],[-92.341207,48.23248],[-92.066269,48.359602],[-91.542512,48.053268],[-90.88548,48.245784],[-90.703702,48.096009],[-89.489226,48.014528],[-90.735927,47.624343],[-92.058888,46.809938],[-92.025789,46.710839],[-91.781928,46.697604],[-90.880358,46.957661],[-90.78804,46.844886],[-90.920813,46.637432],[-90.327548,46.550262],[-89.929158,46.29975],[-88.141001,45.930608],[-88.13364,45.823128],[-87.831442,45.714938],[-87.887828,45.358122],[-87.647454,45.345232],[-87.72796,45.207956],[-87.59188,45.094689],[-87.983065,44.72073],[-87.970702,44.530292],[-87.021088,45.296541],[-87.73063,43.893862],[-87.910172,43.236634],[-87.800477,42.49192],[-90.614589,42.508053],[-91.078097,42.806526],[-91.177728,43.118733],[-91.062562,43.243165],[-91.217706,43.50055]]],[[[-104.053249,41.001406],[-104.053127,43.000585],[-98.568936,42.998537],[-98.042011,42.767316],[-97.834172,42.868794],[-97.256752,42.853913],[-96.409408,42.487595],[-95.850188,41.184798],[-95.885349,40.721093],[-95.336242,40.019104],[-102.051744,40.003078],[-102.051614,41.002377],[-104.053249,41.001406]]],[[[-86.880572,45.331467],[-86.956192,45.351179],[-86.82177,45.427602],[-86.880572,45.331467]]]]},\"properties\":{\"name\":\"Minnesota\",\"nation\":\"USA  \"}}]}","volume":"37","issue":"2","noUsgsAuthors":false,"publicationDate":"2007-06-08","publicationStatus":"PW","scienceBaseUri":"505baa53e4b08c986b3227d1","contributors":{"authors":[{"text":"Winter, T. C.","contributorId":23485,"corporation":false,"usgs":true,"family":"Winter","given":"T.","email":"","middleInitial":"C.","affiliations":[],"preferred":false,"id":398187,"contributorType":{"id":1,"text":"Authors"},"rank":1}]}}
,{"id":70023601,"text":"70023601 - 2001 - Detection of pesticides and pesticide metabolites using the cross reactivity of enzyme immunoassays","interactions":[],"lastModifiedDate":"2022-10-25T17:31:24.461178","indexId":"70023601","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2143,"text":"Journal of AOAC International","active":true,"publicationSubtype":{"id":10}},"title":"Detection of pesticides and pesticide metabolites using the cross reactivity of enzyme immunoassays","docAbstract":"Enzyme immunoassay is an important environmental analysis method that may be used to identify many pesticide analytes in water samples. Because of similarities in chemical structure between various members of a pesticide class, there often may be an unwanted response that is characterized by a percentage of cross reactivity. Also, there may be cross reactivity caused by degradation products of the target analyte that may be present in the sample. In this paper, the concept of cross reactivity caused by degradation products or by nontarget analytes is explored as a tool for identification of metabolites or structurally similar compounds not previously known to be present in water samples. Two examples are examined in this paper from various water quality studies. They are alachlor and its metabolite, alachlor ethane sulfonic acid, and atrazine and its class members, prometryn and propazine. A method for using cross reactivity for the detection of these compounds is explained in this paper.","language":"English","publisher":"Oxford University Press","doi":"10.1093/jaoac/84.1.162","issn":"10603271","usgsCitation":"Thurman, E., and Aga, D., 2001, Detection of pesticides and pesticide metabolites using the cross reactivity of enzyme immunoassays: Journal of AOAC International, v. 84, no. 1, p. 162-167, https://doi.org/10.1093/jaoac/84.1.162.","productDescription":"6 p.","startPage":"162","endPage":"167","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232222,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":408706,"rank":2,"type":{"id":15,"text":"Index Page"},"url":"https://academic.oup.com/jaoac/article/84/1/162/5656441"}],"volume":"84","issue":"1","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"5059ff6be4b0c8380cd4f199","contributors":{"authors":[{"text":"Thurman, E.M.","contributorId":102864,"corporation":false,"usgs":true,"family":"Thurman","given":"E.M.","affiliations":[],"preferred":false,"id":398176,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Aga, D.S.","contributorId":18521,"corporation":false,"usgs":true,"family":"Aga","given":"D.S.","affiliations":[],"preferred":false,"id":398175,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023596,"text":"70023596 - 2001 - Estimating equation for mixed populations of floods in Massachusetts","interactions":[],"lastModifiedDate":"2012-03-12T17:20:02","indexId":"70023596","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2341,"text":"Journal of Hydrologic Engineering","active":true,"publicationSubtype":{"id":10}},"title":"Estimating equation for mixed populations of floods in Massachusetts","docAbstract":"A single equation for estimating the peak flows of annual floods at ungauged sites in Massachusetts was developed by combining the conditional probabilities of floods caused by tropical cyclones and ice-jam releases with the conditional probability of \"ordinary\" floods. Regression equations for these three flood populations demonstrated that two basin characteristics, drainage-basin area and basin head, and frequency of flooding determined the corresponding peak-flow rates.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Journal of Hydrologic Engineering","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1061/(ASCE)1084-0699(2001)6:1(72)","issn":"10840699","usgsCitation":"Murphy, P., 2001, Estimating equation for mixed populations of floods in Massachusetts: Journal of Hydrologic Engineering, v. 6, no. 1, p. 72-74, https://doi.org/10.1061/(ASCE)1084-0699(2001)6:1(72).","startPage":"72","endPage":"74","numberOfPages":"3","costCenters":[],"links":[{"id":207303,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1061/(ASCE)1084-0699(2001)6:1(72)"},{"id":232139,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"6","issue":"1","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505a0b18e4b0c8380cd5257e","contributors":{"authors":[{"text":"Murphy, P.J.","contributorId":91903,"corporation":false,"usgs":true,"family":"Murphy","given":"P.J.","email":"","affiliations":[],"preferred":false,"id":398164,"contributorType":{"id":1,"text":"Authors"},"rank":1}]}}
,{"id":70023594,"text":"70023594 - 2001 - A functional relation for field-scale nonaqueous phase liquid dissolution developed using a pore network model","interactions":[],"lastModifiedDate":"2018-12-03T09:01:54","indexId":"70023594","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":"A functional relation for field-scale nonaqueous phase liquid dissolution developed using a pore network model","docAbstract":"<div id=\"abstracts\" class=\"Abstracts\"><div id=\"aep-abstract-id16\" class=\"abstract author\"><div id=\"aep-abstract-sec-id17\"><p><span>A pore network&nbsp;model&nbsp;with cubic chambers and rectangular&nbsp;tubes&nbsp;was used to estimate the&nbsp;nonaqueous phase liquid&nbsp;(NAPL) dissolution rate coefficient,&nbsp;</span><i>K</i><sub>diss</sub><i>a</i><sub>i</sub><span>, and NAPL/water total specific interfacial&nbsp;area,&nbsp;</span><i>a</i><sub>i</sub>.<span>&nbsp;</span><i>K</i><sub>diss</sub><i>a</i><sub>i</sub><span>&nbsp;was computed as a function of modified&nbsp;Peclet number(</span><i>Pe</i><span>′) for various&nbsp;NAPL&nbsp;saturations (</span><i>S</i><sub>N</sub>) and<span>&nbsp;</span><i>a</i><sub>i</sub><span>&nbsp;during&nbsp;drainage&nbsp;and&nbsp;imbibition&nbsp;and during dissolution without displacement. The largest contributor to&nbsp;</span><i>a</i><sub>i</sub><span>&nbsp;</span>was the interfacial area in the water-filled corners of chambers and tubes containing NAPL. When<span>&nbsp;</span><i>K</i><sub>diss</sub><i>a</i><sub>i</sub><span>&nbsp;</span>was divided by<span>&nbsp;</span><i>a</i><sub>i</sub>, the resulting curves of dissolution coefficient,<span>&nbsp;</span><i>K</i><sub>diss</sub><span>&nbsp;</span>versus<span>&nbsp;</span><i>Pe</i>′ suggested that an approximate value of<span>&nbsp;</span><i>K</i><sub>diss</sub><span>&nbsp;could be obtained as a weak function of&nbsp;hysteresis&nbsp;or&nbsp;</span><i>S</i><sub>N</sub>. Spatially and temporally variable maps of<span>&nbsp;</span><i>K</i><sub>diss</sub><i>a</i><sub>i</sub><span>&nbsp;calculated using the network model were used in&nbsp;field-scale&nbsp;simulations of NAPL dissolution. These simulations were compared to simulations using a constant value of&nbsp;</span><i>K</i><sub>diss</sub><i>a</i><sub>i</sub><span>&nbsp;and the empirical&nbsp;correlation&nbsp;of Powers et al. [Water Resour. Res. 30(2) (1994b) 321]. Overall, a methodology was developed for incorporating&nbsp;pore-scale&nbsp;processes into field-scale&nbsp;prediction&nbsp;of NAPL dissolution.</span></p></div></div></div>","language":"English","publisher":"Elsevier","doi":"10.1016/S0169-7722(00)00171-6","issn":"01697722","usgsCitation":"Dillard, L., Essaid, H., and Blunt, M., 2001, A functional relation for field-scale nonaqueous phase liquid dissolution developed using a pore network model: Journal of Contaminant Hydrology, v. 48, no. 1-2, p. 89-119, https://doi.org/10.1016/S0169-7722(00)00171-6.","productDescription":"31 p.","startPage":"89","endPage":"119","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232741,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207628,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1016/S0169-7722(00)00171-6"}],"volume":"48","issue":"1-2","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"5059e3e5e4b0c8380cd462ad","contributors":{"authors":[{"text":"Dillard, L.A.","contributorId":32695,"corporation":false,"usgs":true,"family":"Dillard","given":"L.A.","email":"","affiliations":[],"preferred":false,"id":398159,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Essaid, H.I.","contributorId":22342,"corporation":false,"usgs":true,"family":"Essaid","given":"H.I.","email":"","affiliations":[],"preferred":false,"id":398158,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Blunt, M.J.","contributorId":40764,"corporation":false,"usgs":true,"family":"Blunt","given":"M.J.","email":"","affiliations":[],"preferred":false,"id":398160,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023593,"text":"70023593 - 2001 - Regional water-quality analysis of 2,4-D and dicamba in river water using gas chromatography-isotope dilution mass spectrometry","interactions":[],"lastModifiedDate":"2018-11-30T06:57:21","indexId":"70023593","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2040,"text":"International Journal of Environmental Analytical Chemistry","active":true,"publicationSubtype":{"id":10}},"title":"Regional water-quality analysis of 2,4-D and dicamba in river water using gas chromatography-isotope dilution mass spectrometry","docAbstract":"<div class=\"hlFld-Abstract test\"><div class=\"abstractSection abstractInFull\"><p>Gas chromatography with isotope dilution mass spectrometry (GC-MS) and enzyme-linked immunosorbent assay (ELISA) were used in regional National Water Quality Assessment studies of the herbicides, 2,4-D and dicamba, in river water across the United States. The GC-MS method involved solid-phase extraction, derivatized with deuterated 2,4-D, and analysis by selected ion monitoring. The ELISA method was applied after preconcentration with solid-phase extraction. The ELISA method was unreliable because of interference from humic substances that were also isolated by solid-phase extraction. Therefore, GC-MS was used to analyzed 80 samples from river water from 14 basins. The frequency of detection of dicamba (28%) was higher than that for 2,4-D (16%). Concentrations were higher for dicamba than for 2,4-D, ranging from less than the detection limit (7lt; 0.05 μg/L) to 3.77μg/L, in spite of 5 times more annual use of 2,4-D as compared to dicamba. These results suggest that 2,4-D degrades more rapidly in the environment than dicamba.</p></div></div>","language":"English","publisher":"Taylor & Francis","doi":"10.1080/03067310108044398","issn":"03067319","usgsCitation":"Thurman, E., Zimmerman, L., Aga, D., and Gilliom, R.J., 2001, Regional water-quality analysis of 2,4-D and dicamba in river water using gas chromatography-isotope dilution mass spectrometry: International Journal of Environmental Analytical Chemistry, v. 79, no. 3, p. 185-198, https://doi.org/10.1080/03067310108044398.","productDescription":"14 p.","startPage":"185","endPage":"198","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232740,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"79","issue":"3","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"50e4a5a1e4b0e8fec6cdbeaf","contributors":{"authors":[{"text":"Thurman, E.M.","contributorId":102864,"corporation":false,"usgs":true,"family":"Thurman","given":"E.M.","affiliations":[],"preferred":false,"id":398157,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Zimmerman, L.R.","contributorId":28624,"corporation":false,"usgs":true,"family":"Zimmerman","given":"L.R.","email":"","affiliations":[],"preferred":false,"id":398155,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Aga, D.S.","contributorId":18521,"corporation":false,"usgs":true,"family":"Aga","given":"D.S.","affiliations":[],"preferred":false,"id":398154,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Gilliom, R. J.","contributorId":60650,"corporation":false,"usgs":true,"family":"Gilliom","given":"R.","email":"","middleInitial":"J.","affiliations":[],"preferred":false,"id":398156,"contributorType":{"id":1,"text":"Authors"},"rank":4}]}}
,{"id":70023589,"text":"70023589 - 2001 - Molecular resolution and fragmentation of fulvic acid by electrospray ionization/multistage tandem mass spectrometry","interactions":[],"lastModifiedDate":"2018-12-03T08:05:21","indexId":"70023589","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":761,"text":"Analytical Chemistry","active":true,"publicationSubtype":{"id":10}},"title":"Molecular resolution and fragmentation of fulvic acid by electrospray ionization/multistage tandem mass spectrometry","docAbstract":"Molecular weight distributions of fulvic acid from the Suwannee River, Georgia, were investigated by electrospray ionization/quadrupole mass spectrometry (ESI/QMS), and fragmentation pathways of specific fulvic acid masses were investigated by electrospray ionization/ion trap multistage tandem mass spectrometry (ESI/MST/MS). ESI/QMS studies of the free acid form of low molecular weight poly(carboxylic acid) standards in 75% methanol/25% water mobile phase found that negative ion detection gave the optimum generation of parent ions that can be used for molecular weight determinations. However, experiments with poly(acrylic acid) mixtures and specific high molecular weight standards found multiply charged negative ions that gave a low bias to molecular mass distributions. The number of negative charges on a molecule is dependent on the distance between charges. ESI/MST/MS of model compounds found characteristic water loss from alcohol dehydration and anhydride formation, as well as CO2 loss from decarboxylation, and CO loss from ester structures. Application of these fragmentation pathways to specific masses of fulvic acid isolated and fragmented by ESI/MST/MS is indicative of specific structures that can serve as a basis for future structural confirmation after these hypothesized structures are synthesized.","language":"English","publisher":"ACS","doi":"10.1021/ac0012593","issn":"00032700","usgsCitation":"Leenheer, J., Rostad, C., Gates, P.M., Furlong, E., and Ferrer, I., 2001, Molecular resolution and fragmentation of fulvic acid by electrospray ionization/multistage tandem mass spectrometry: Analytical Chemistry, v. 73, no. 7, p. 1461-1471, https://doi.org/10.1021/ac0012593.","productDescription":"11 p.","startPage":"1461","endPage":"1471","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232657,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207588,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1021/ac0012593"}],"volume":"73","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-03-07","publicationStatus":"PW","scienceBaseUri":"505a5d10e4b0c8380cd7012d","contributors":{"authors":[{"text":"Leenheer, J.A.","contributorId":75123,"corporation":false,"usgs":true,"family":"Leenheer","given":"J.A.","affiliations":[],"preferred":false,"id":398146,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Rostad, C.E.","contributorId":50939,"corporation":false,"usgs":true,"family":"Rostad","given":"C.E.","email":"","affiliations":[],"preferred":false,"id":398145,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Gates, Paul M.","contributorId":31411,"corporation":false,"usgs":true,"family":"Gates","given":"Paul","email":"","middleInitial":"M.","affiliations":[],"preferred":false,"id":398144,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Furlong, E. T. 0000-0002-7305-4603","orcid":"https://orcid.org/0000-0002-7305-4603","contributorId":98346,"corporation":false,"usgs":true,"family":"Furlong","given":"E. T.","affiliations":[],"preferred":false,"id":398148,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Ferrer, I.","contributorId":97260,"corporation":false,"usgs":true,"family":"Ferrer","given":"I.","email":"","affiliations":[],"preferred":false,"id":398147,"contributorType":{"id":1,"text":"Authors"},"rank":5}]}}
,{"id":70023580,"text":"70023580 - 2001 - Occurrence of cyanazine compounds in groundwater: Degradates more prevalent than the parent compound","interactions":[],"lastModifiedDate":"2018-11-30T06:36:38","indexId":"70023580","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":"Occurrence of cyanazine compounds in groundwater: Degradates more prevalent than the parent compound","docAbstract":"<p>A recently developed analytical method using liquid chromatography/mass spectrometry was used to investigate the occurrence of cyanazine and its degradates cyanazine acid (CAC), cyanazine amide (CAM), deethylcyanazine (DEC), and deethylcyanazine acid (DCAC) in groundwater. This research represents some of the earliest data on the occurrence of cyanazine degradates in groundwater. Although cyanazine was infrequently detected in the 64 wells across Iowa sampled in 1999, cyanazine degradates were commonly found during this study. The most frequently detected cyanazine compound was DCAC (32.8%) followed by CAC (29.7%), CAM (17.2%), DEC (3.1%), and cyanazine (3.1%). The frequency of detection for cyanazine or one or more of its degradates (CYTOT) was more than 12-fold over that of cyanazine alone (39.1% for CYTOT versus 3.1% for cyanazine). Of the total measured concentration of cyanazine, only 0.2% was derived from its parent compound - with DCAC (74.1%) and CAC (18.4%) comprising 92.5% of this total. Thus, although DCAC and CAC had similar frequencies of detection, DCAC was generally present in higher concentrations. No concentrations of cyanazine compounds for this study exceeded water-quality criteria for the protection of human health. Only cyanazine, however, has such a criteria established. Nevertheless, because these cyanazine degradates are still chlorinated, they may have similar toxicity as their parent compound - similar to what has been found with the chlorinated degradates of atrazine. Thus, the results of this study documented that data on the degradates for cyanazine are critical for understanding its fate and transport in the hydrologic system. Furthermore, the prevalence of the chlorinated degradates of cyanazine found in groundwater suggests that to accurately determine the overall effect on human health and the environment from cyanazine its degradates should also be considered. In addition, because CYTOT was found in 57.6% of the samples collected from alluvial aquifers, about 2-5 times more frequently than the other major aquifer types (glacial drift, bedrock/karst, bedrock/nonkarst) under investigation, this finding has long-term implications for the occurrence of CYTOT in streams. It is anticipated that low-level concentrations of CYTOT will continue to be detected in streams for years after the use of cyanazine has terminated (scheduled for the year 2000 in the United States), primarily through its movement from groundwater into streams during base-flow conditions.</p>","language":"English","publisher":"American Chemical Society","doi":"10.1021/es001520x","issn":"0013936X","usgsCitation":"Kolpin, D., Thurman, E., and Linhart, S.M., 2001, Occurrence of cyanazine compounds in groundwater: Degradates more prevalent than the parent compound: Environmental Science & Technology, v. 35, no. 6, p. 1217-1222, https://doi.org/10.1021/es001520x.","productDescription":"6 p.","startPage":"1217","endPage":"1222","onlineOnly":"N","additionalOnlineFiles":"N","costCenters":[{"id":351,"text":"Iowa Water Science Center","active":true,"usgs":true},{"id":589,"text":"Toxic Substances Hydrology 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M.","contributorId":102517,"corporation":false,"usgs":true,"family":"Linhart","given":"S.","email":"","middleInitial":"M.","affiliations":[],"preferred":false,"id":398109,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023575,"text":"70023575 - 2001 - Sources of global warming in upper ocean temperature during El Niño","interactions":[],"lastModifiedDate":"2015-05-12T14:02:29","indexId":"70023575","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2315,"text":"Journal of Geophysical Research C: Oceans","active":true,"publicationSubtype":{"id":10}},"title":"Sources of global warming in upper ocean temperature during El Niño","docAbstract":"<p><span>Global average sea surface temperature (SST) from 40&deg;S to 60&deg;N fluctuates &plusmn;0.3&deg;C on interannual period scales, with global warming (cooling) during El Ni&ntilde;o (La Ni&ntilde;a). About 90% of the global warming during El Ni&ntilde;o occurs in the tropical global ocean from 20&deg;S to 20&deg;N, half because of large SST anomalies in the tropical Pacific associated with El Ni&ntilde;o and the other half because of warm SST anomalies occurring over &sim;80% of the tropical global ocean. From examination of National Centers for Environmental Prediction [</span><i>Kalnay et al.</i><span>, 1996] and Comprehensive Ocean-Atmosphere Data Set [</span><i>Woodruff et al.</i><span>, 1993] reanalyses, tropical global warming during El Ni&ntilde;o is associated with higher troposphere moisture content and cloud cover, with reduced trade wind intensity occurring during the onset phase of El Ni&ntilde;o. During this onset phase the tropical global average diabatic heat storage tendency in the layer above the main pycnocline is 1&ndash;3 W m</span><sup>&minus;2</sup><span>above normal. Its principal source is a reduction in the poleward Ekman heat flux out of the tropical ocean of 2&ndash;5 W m</span><sup>&minus;2</sup><span>. Subsequently, peak tropical global warming during El Ni&ntilde;o is dissipated by an increase in the flux of latent heat to the troposphere of 2&ndash;5 W m</span><sup>&minus;2</sup><span>, with reduced shortwave and longwave radiative fluxes in response to increased cloud cover tending to cancel each other. In the extratropical global ocean the reduction in poleward Ekman heat flux out of the tropics during the onset of El Ni&ntilde;o tends to be balanced by reduction in the flux of latent heat to the troposphere. Thus global warming and cooling during Earth's internal mode of interannual climate variability arise from fluctuations in the global hydrological balance, not the global radiation balance. Since it occurs in the absence of extraterrestrial and anthropogenic forcing, global warming on decadal, interdecadal, and centennial period scales may also occur in association with Earth's internal modes of climate variability on those scales.</span></p>","language":"English","publisher":"Wiley","doi":"10.1029/1999JC000130","issn":"01480227","usgsCitation":"White, W.B., Cayan, D.R., Dettinger, M., and Auad, G., 2001, Sources of global warming in upper ocean temperature during El Niño: Journal of Geophysical Research C: Oceans, v. 106, no. C3, p. 4349-4367, https://doi.org/10.1029/1999JC000130.","productDescription":"19 p.","startPage":"4349","endPage":"4367","onlineOnly":"N","additionalOnlineFiles":"N","costCenters":[],"links":[{"id":489785,"rank":1,"type":{"id":40,"text":"Open Access Publisher Index Page"},"url":"https://doi.org/10.1029/1999jc000130","text":"Publisher Index Page"},{"id":232374,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"106","issue":"C3","noUsgsAuthors":false,"publicationDate":"2001-03-15","publicationStatus":"PW","scienceBaseUri":"505b937ae4b08c986b31a4f5","contributors":{"authors":[{"text":"White, Warren B.","contributorId":26111,"corporation":false,"usgs":true,"family":"White","given":"Warren","email":"","middleInitial":"B.","affiliations":[],"preferred":false,"id":398088,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Cayan, Daniel R. 0000-0002-2719-6811 drcayan@usgs.gov","orcid":"https://orcid.org/0000-0002-2719-6811","contributorId":1494,"corporation":false,"usgs":true,"family":"Cayan","given":"Daniel","email":"drcayan@usgs.gov","middleInitial":"R.","affiliations":[],"preferred":false,"id":398087,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Dettinger, Mike 0000-0002-7509-7332 mddettin@usgs.gov","orcid":"https://orcid.org/0000-0002-7509-7332","contributorId":859,"corporation":false,"usgs":true,"family":"Dettinger","given":"Mike","email":"mddettin@usgs.gov","affiliations":[{"id":438,"text":"National Research Program - Western Branch","active":true,"usgs":true}],"preferred":false,"id":398090,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Auad, Guillermo","contributorId":78120,"corporation":false,"usgs":true,"family":"Auad","given":"Guillermo","email":"","affiliations":[],"preferred":false,"id":398089,"contributorType":{"id":1,"text":"Authors"},"rank":4}]}}
,{"id":70023571,"text":"70023571 - 2001 - Methyl tert‐butyl ether degradation in the unsaturated zone and the relation between MTBE in the atmosphere and shallow groundwater","interactions":[],"lastModifiedDate":"2018-11-28T10:35:28","indexId":"70023571","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":3722,"text":"Water Resources Research","onlineIssn":"1944-7973","printIssn":"0043-1397","active":true,"publicationSubtype":{"id":10}},"title":"Methyl tert‐butyl ether degradation in the unsaturated zone and the relation between MTBE in the atmosphere and shallow groundwater","docAbstract":"<p><span>Atmospheric methyl tert‐butyl ether (MTBE) concentrations in southern New Jersey generally exceeded concentrations in samples taken from the unsaturated zone. A simple unsaturated zone transport model indicates that MTBE degradation can explain the attenuation with half‐lives from a few months to a couple of years. Tert‐butyl alcohol (TBA), a possible degradation product of MTBE, was detected in unsaturated‐zone samples at concentrations exceeding atmospheric levels at some sites, suggesting the possible conversion of MTBE to TBA. At sites where MTBE was detected in shallow groundwater, the concentration was typically higher than the overlying unsaturated‐zone concentration. This observation is consistent with outgassing from the aquifer and combined with the unsaturated‐zone attenuation suggests some of the MTBE detections in shallow groundwater are nonatmospheric in origin, coming from leaking tanks, road runoff, or other sources. The identification of sources of MTBE in groundwater and attenuation mechanisms through the hydrologic cycle is critical in developing an understanding of the long‐term effect of MTBE releases.</span></p>","language":"English","publisher":"American Geophysical Union","doi":"10.1029/2000WR900292","usgsCitation":"Baehr, A.L., Charles, E., and Baker, R.J., 2001, Methyl tert‐butyl ether degradation in the unsaturated zone and the relation between MTBE in the atmosphere and shallow groundwater: Water Resources Research, v. 37, no. 2, p. 223-233, https://doi.org/10.1029/2000WR900292.","productDescription":"11 p.","startPage":"223","endPage":"233","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":488090,"rank":1,"type":{"id":40,"text":"Open Access Publisher Index Page"},"url":"https://doi.org/10.1029/2000wr900292","text":"Publisher Index Page"},{"id":232333,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"37","issue":"2","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505a5616e4b0c8380cd6d348","contributors":{"authors":[{"text":"Baehr, Arthur L.","contributorId":104523,"corporation":false,"usgs":true,"family":"Baehr","given":"Arthur","email":"","middleInitial":"L.","affiliations":[],"preferred":false,"id":398078,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Charles, Emmanuel G. 0000-0002-3338-4958","orcid":"https://orcid.org/0000-0002-3338-4958","contributorId":3637,"corporation":false,"usgs":false,"family":"Charles","given":"Emmanuel G.","affiliations":[],"preferred":false,"id":398077,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Baker, Ronald J. rbaker@usgs.gov","contributorId":1436,"corporation":false,"usgs":true,"family":"Baker","given":"Ronald","email":"rbaker@usgs.gov","middleInitial":"J.","affiliations":[{"id":470,"text":"New Jersey Water Science Center","active":true,"usgs":true}],"preferred":true,"id":398079,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023560,"text":"70023560 - 2001 - User interface for ground-water modeling: Arcview extension","interactions":[],"lastModifiedDate":"2012-03-12T17:20:01","indexId":"70023560","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2341,"text":"Journal of Hydrologic Engineering","active":true,"publicationSubtype":{"id":10}},"title":"User interface for ground-water modeling: Arcview extension","docAbstract":"Numerical simulation for ground-water modeling often involves handling large input and output data sets. A geographic information system (GIS) provides an integrated platform to manage, analyze, and display disparate data and can greatly facilitate modeling efforts in data compilation, model calibration, and display of model parameters and results. Furthermore, GIS can be used to generate information for decision making through spatial overlay and processing of model results. Arc View is the most widely used Windows-based GIS software that provides a robust user-friendly interface to facilitate data handling and display. An extension is an add-on program to Arc View that provides additional specialized functions. An Arc View interface for the ground-water flow and transport models MODFLOW and MT3D was built as an extension for facilitating modeling. The extension includes preprocessing of spatially distributed (point, line, and polygon) data for model input and postprocessing of model output. An object database is used for linking user dialogs and model input files. The Arc View interface utilizes the capabilities of the 3D Analyst extension. Models can be automatically calibrated through the Arc View interface by external linking to such programs as PEST. The efficient pre- and postprocessing capabilities and calibration link were demonstrated for ground-water modeling in southwest Kansas.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Journal of Hydrologic Engineering","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1061/(ASCE)1084-0699(2001)6:3(251)","issn":"10840699","usgsCitation":"Tsou, M., and Whittemore, D.O., 2001, User interface for ground-water modeling: Arcview extension: Journal of Hydrologic Engineering, v. 6, no. 3, p. 251-257, https://doi.org/10.1061/(ASCE)1084-0699(2001)6:3(251).","startPage":"251","endPage":"257","numberOfPages":"7","costCenters":[],"links":[{"id":232176,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207323,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1061/(ASCE)1084-0699(2001)6:3(251)"}],"volume":"6","issue":"3","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505bbfc5e4b08c986b329d68","contributors":{"authors":[{"text":"Tsou, Ming-shu","contributorId":20507,"corporation":false,"usgs":false,"family":"Tsou","given":"Ming-shu","email":"","affiliations":[],"preferred":false,"id":398039,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Whittemore, Donald O.","contributorId":28748,"corporation":false,"usgs":false,"family":"Whittemore","given":"Donald","email":"","middleInitial":"O.","affiliations":[],"preferred":false,"id":398040,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023559,"text":"70023559 - 2001 - Evaluation of mixed-population flood-frequency analysis","interactions":[],"lastModifiedDate":"2012-03-12T17:20:02","indexId":"70023559","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2341,"text":"Journal of Hydrologic Engineering","active":true,"publicationSubtype":{"id":10}},"title":"Evaluation of mixed-population flood-frequency analysis","docAbstract":"A mixed population of flood flows was shown to cause quality-of-fit problems if a single-population flood-frequency distribution was used to describe the flood data. The three populations in this mix were \"ordinary,\" tropical cyclone, and ice-jam-release floods. Parametric descriptions of the single and separated flood populations were evaluated using probability-plot correlation-coefficient tests. These tests quantified how well the flood-probability distributions agreed with plotting-position descriptions of the data and quantified the differences due to the mixed-population analysis. High outliers caused the high skewness found in the single- population analyses. The tropical cyclone component was underestimated by single-population analyses at gauging stations in Massachusetts that had little data.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Journal of Hydrologic Engineering","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1061/(ASCE)1084-0699(2001)6:1(62)","issn":"10840699","usgsCitation":"Murphy, P., 2001, Evaluation of mixed-population flood-frequency analysis: Journal of Hydrologic Engineering, v. 6, no. 1, p. 62-70, https://doi.org/10.1061/(ASCE)1084-0699(2001)6:1(62).","startPage":"62","endPage":"70","numberOfPages":"9","costCenters":[],"links":[{"id":207302,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1061/(ASCE)1084-0699(2001)6:1(62)"},{"id":232138,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"6","issue":"1","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505a0c9be4b0c8380cd52c06","contributors":{"authors":[{"text":"Murphy, P.J.","contributorId":91903,"corporation":false,"usgs":true,"family":"Murphy","given":"P.J.","email":"","affiliations":[],"preferred":false,"id":398038,"contributorType":{"id":1,"text":"Authors"},"rank":1}]}}
,{"id":70023557,"text":"70023557 - 2001 - Urbanization effects on the hydrology of the Atlanta, Georgia (USA)","interactions":[],"lastModifiedDate":"2012-03-12T17:20:10","indexId":"70023557","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":"Urbanization effects on the hydrology of the Atlanta, Georgia (USA)","docAbstract":"For the period from 1958 to 1996, streamflow and rainfall characteristics of a highly urbanized watershed were compared with less-urbanized and non-urbanized watersheds in the vicinity of Atlanta, Georgia (USA). Water levels in several wells completed in surficial and crystalline-rock aquifers also were evaluated. Annual runoff coefficients (runoff as a fractional percentage of precipitation) ranged from 0.31 to 0.34 and were not significantly different for the urban stream (Peachtree Creek). Peak flows for the largest 25 stormflows at Peachtree Creek were 30% to 80% greater than peak flows for the other streams. A 2-day storm recession constant for Peachtree Creek was much larger, that is streamflow decreased more rapidly than for the other streams. Average low flow of Peachtree Creek was 25 to 35% less than the other streams, possibly the result of decreased infiltration caused by the more efficient routing of storm water and the paving of groundwater recharge areas. The timing of groundwater level variations was similar annually in each well, reflecting the seasonal recharge. Although water level monitoring only began during the late 1970s and early 1980s for the two urban wells, water levels in these wells have been declining compared to non-urban wells since then. The water level decline is attributed to decreased groundwater recharge in the urban watersheds due to increased imperviousness and related rapid storm runoff. Likewise, the increased urbanization from the 1960s to the 1990s of the Peachtree Creek watershed produced more runoff than urbanization in the less urbanized Big Creek and Sweetwater Creek watersheds.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"IAHS-AISH Publication","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","issn":"01447815","usgsCitation":"Peters, N., and Rose, S., 2001, Urbanization effects on the hydrology of the Atlanta, Georgia (USA): IAHS-AISH Publication, no. 269, p. 109-116.","startPage":"109","endPage":"116","numberOfPages":"8","costCenters":[],"links":[{"id":232739,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"issue":"269","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505bbe45e4b08c986b3294c6","contributors":{"authors":[{"text":"Peters, N.E.","contributorId":33332,"corporation":false,"usgs":true,"family":"Peters","given":"N.E.","email":"","affiliations":[],"preferred":false,"id":398035,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Rose, S.","contributorId":56002,"corporation":false,"usgs":true,"family":"Rose","given":"S.","email":"","affiliations":[],"preferred":false,"id":398036,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023555,"text":"70023555 - 2001 - Effect of the 1997-1998 ENSO-related drought on hydrology and salinity in a Micronesian wetland complex","interactions":[],"lastModifiedDate":"2022-10-13T16:10:50.202353","indexId":"70023555","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":1583,"text":"Estuaries","active":true,"publicationSubtype":{"id":10}},"title":"Effect of the 1997-1998 ENSO-related drought on hydrology and salinity in a Micronesian wetland complex","docAbstract":"<div id=\"Abs1-section\" class=\"c-article-section\"><div id=\"Abs1-content\" class=\"c-article-section__content\"><p>The potential effects of global climate change on coastal ecosystems have attracted considerable attention, but the impacts of shorter-term climate perturbations such as ENSO (El Niño-Southern Oscillation) are lesser known. In this study, we determined the effects of the 1997–1998 ENSO-related drought on the hydrology and salinity of a Micronesian mangrove ecosystem and an adjacent freshwater swamp. A network of 9 piezometer clusters installed at the study site served as sampling points for continuous and manual measurements of salinity and water level. During the drought period from January through April 1998, mean water table levels in the mangroves and freshwater swamp were approximately 12 and 54 cm lower, respectively, than during May through December when precipitation returned to near normal levels. At the peak of the drought (February 1998), the most dramatic result was a reversal in groundwater flow that sent groundwater from the mangroves upstream toward the freshwater swamp. Flow nets constructed for this period and immediately after illustrate the strong hydrological linkage between the two systems. This linkage was also illustrated by measurements of groundwater salinity in the piezometer network. Ninety-six percent of the salinity measurements taken in the mangroves during the study were at least 10‰ less than the salinity of sea water, indicating that the mangroves were consistently receiving freshwater flows. An analysis of variance of groundwater salinity measurements during and after the drought showed that salinity levels in the 0.5 and 1.0 m depth piezometers were greater during than after the drought. In a comparison of salinity values in 0.5-m wells during low tide, mean salinity was approximately twice as high during the drought than after (14.7‰ versus 6.2‰, respectively). This study demonstrates that short-term climate perturbations such as ENSO can disrupt important coastal processes. Over repeated drought cycles, such perturbations have the potential to affect the structure and function of mangrove forests and upstream ecosystems.</p></div></div>","language":"English","publisher":"Springer","doi":"10.2307/1353237","issn":"01608347","usgsCitation":"Drexler, J., and Ewel, K.C., 2001, Effect of the 1997-1998 ENSO-related drought on hydrology and salinity in a Micronesian wetland complex: Estuaries, v. 24, no. 3, p. 347-356, https://doi.org/10.2307/1353237.","productDescription":"10 p.","startPage":"347","endPage":"356","costCenters":[],"links":[{"id":232697,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"country":"Micronesia","otherGeospatial":"Kosrae","geographicExtents":"{\n  \"type\": \"FeatureCollection\",\n  \"features\": [\n    {\n      \"type\": \"Feature\",\n      \"properties\": {},\n      \"geometry\": {\n        \"type\": \"Polygon\",\n        \"coordinates\": [\n          [\n            [\n         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162.9986572265625,\n              5.2567772244185464\n            ],\n            [\n              163.01204681396484,\n              5.262589136408595\n            ]\n          ]\n        ]\n      }\n    }\n  ]\n}","volume":"24","issue":"3","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505a0614e4b0c8380cd510f9","contributors":{"authors":[{"text":"Drexler, J.Z. 0000-0002-0127-3866","orcid":"https://orcid.org/0000-0002-0127-3866","contributorId":54766,"corporation":false,"usgs":true,"family":"Drexler","given":"J.Z.","affiliations":[],"preferred":false,"id":398028,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Ewel, K. C.","contributorId":70352,"corporation":false,"usgs":true,"family":"Ewel","given":"K.","email":"","middleInitial":"C.","affiliations":[],"preferred":false,"id":398029,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023554,"text":"70023554 - 2001 - Methyl tert-butyl ether biodegradation by indigenous aquifer microorganisms under natural and artificial oxic conditions","interactions":[],"lastModifiedDate":"2018-12-03T08:38:44","indexId":"70023554","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":"Methyl tert-butyl ether biodegradation by indigenous aquifer microorganisms under natural and artificial oxic conditions","docAbstract":"<div class=\"hlFld-Abstract\"><div id=\"abstractBox\"><p class=\"articleBody_abstractText\">Microbial communities indigenous to a shallow groundwater system near Beaufort, SC, degraded milligram per liter concentrations of methyl<span>&nbsp;</span><i>tert</i>-butyl ether (MTBE) under natural and artificial oxic conditions. Significant MTBE biodegradation was observed where anoxic, MTBE-contaminated groundwater discharged to a concrete-lined ditch. In the anoxic groundwater adjacent to the ditch, concentrations of MTBE were &gt;1 mg/L. Where groundwater discharge occurs, dissolved oxygen (DO) concentrations beneath the ditch exceeded 1.0 mg/L to a depth of 1.5 m, and MTBE concentrations decreased to &lt;1 μg/L prior to discharge. MTBE mass flux calculations indicate that 96% of MTBE mass loss occurs in the relatively small oxic zone prior to discharge. Samples of a natural microbial biofilm present in the oxic zone beneath the ditch completely degraded [U-<sup>14</sup>C]MTBE to [<sup>14</sup>C]CO<sub>2</sub><span>&nbsp;</span>in laboratory liquid culture studies, with no accumulation of intermediate compounds. Upgradient of the ditch in the anoxic, MTBE- and BTEX-contaminated aquifer, addition of a soluble oxygen release compound resulted in oxic conditions and rapid MTBE biodegradation by indigenous microorganisms. In an observation well located closest to the oxygen addition area, DO concentrations increased from 0.4 to 12 mg/L in &lt;60 days and MTBE concentrations decreased from 20 to 3 mg/L. In the same time period at a downgradient observation well, DO increased from &lt;0.2 to 2 mg/L and MTBE concentrations decreased from 30 to &lt;5 mg/L. These results indicate that microorganisms indigenous to the groundwater system at this site can degrade milligram per liter concentrations of MTBE under natural and artificial oxic conditions.</p></div></div>","language":"English","publisher":"ACS","doi":"10.1021/es0013879","issn":"0013936X","usgsCitation":"Landmeyer, J., Chapelle, F.H., Herlong, H., and Bradley, P., 2001, Methyl tert-butyl ether biodegradation by indigenous aquifer microorganisms under natural and artificial oxic conditions: Environmental Science & Technology, v. 35, no. 6, p. 1118-1126, https://doi.org/10.1021/es0013879.","productDescription":"9 p.","startPage":"1118","endPage":"1126","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232696,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207605,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1021/es0013879"}],"volume":"35","issue":"6","noUsgsAuthors":false,"publicationDate":"2001-02-10","publicationStatus":"PW","scienceBaseUri":"505a5616e4b0c8380cd6d345","contributors":{"authors":[{"text":"Landmeyer, J. E.","contributorId":91140,"corporation":false,"usgs":true,"family":"Landmeyer","given":"J. E.","affiliations":[],"preferred":false,"id":398025,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Chapelle, F. H.","contributorId":101697,"corporation":false,"usgs":true,"family":"Chapelle","given":"F.","email":"","middleInitial":"H.","affiliations":[],"preferred":false,"id":398026,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Herlong, H.H.","contributorId":106391,"corporation":false,"usgs":true,"family":"Herlong","given":"H.H.","email":"","affiliations":[],"preferred":false,"id":398027,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Bradley, P. M. 0000-0001-7522-8606","orcid":"https://orcid.org/0000-0001-7522-8606","contributorId":29465,"corporation":false,"usgs":true,"family":"Bradley","given":"P. M.","affiliations":[],"preferred":false,"id":398024,"contributorType":{"id":1,"text":"Authors"},"rank":4}]}}
,{"id":70023547,"text":"70023547 - 2001 - Natural attenuation of volatile organic compounds (VOCs) in the leachate plume of a municipal landfill: Using alkylbenzenes as process probes","interactions":[],"lastModifiedDate":"2018-12-03T10:01:47","indexId":"70023547","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":"Natural attenuation of volatile organic compounds (VOCs) in the leachate plume of a municipal landfill: Using alkylbenzenes as process probes","docAbstract":"More than 70 individual VOCs were identified in the leachate plume of a closed municipal landfill. Concentrations were low when compared with data published for other landfills, and total VOCs accounted for less than 0.1% of the total dissolved organic carbon. The VOC concentrations in the core of the anoxic leachate plume are variable, but in all cases they were found to be near or below detection limits within 200 m of the landfall. In contrast to the VOCs, the distributions of chloride ion, a conservative tracer, and nonvolatile dissolved organic carbon, indicate little dilution over the same distance. Thus, natural attentuation processes are effectively limiting migration of the VOC plume. The distribution of C2-3-benzenes, paired on the basis of their octanol-water partition coefficients and Henry's law constants, were systematically evaluated to assess the relative importance of volatilization, sorption, and biodegradation as attenuation mechanisms. Based on our data, biodegradation appears to be the process primarily responsible for the observed attenuation of VOCs at this site. We believe that the alkylbenzenes are powerful process probes that can and should be exploited in studies of natural attenuation in contaminated ground water systems.","language":"English","publisher":"Wiley","doi":"10.1111/j.1745-6584.2001.tb02300.x","issn":"0017467X","usgsCitation":"Eganhouse, R., Cozzarelli, I.M., Scholl, M.A., and Matthews, L., 2001, Natural attenuation of volatile organic compounds (VOCs) in the leachate plume of a municipal landfill: Using alkylbenzenes as process probes: Groundwater, v. 39, no. 2, p. 192-202, https://doi.org/10.1111/j.1745-6584.2001.tb02300.x.","productDescription":"11 p.","startPage":"192","endPage":"202","numberOfPages":"11","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232572,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"39","issue":"2","noUsgsAuthors":false,"publicationDate":"2005-12-13","publicationStatus":"PW","scienceBaseUri":"505a62e1e4b0c8380cd72177","contributors":{"authors":[{"text":"Eganhouse, Robert P. eganhous@usgs.gov","contributorId":2031,"corporation":false,"usgs":true,"family":"Eganhouse","given":"Robert P.","email":"eganhous@usgs.gov","affiliations":[{"id":436,"text":"National Research Program - Eastern Branch","active":true,"usgs":true}],"preferred":true,"id":397994,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Cozzarelli, Isabelle M. 0000-0002-5123-1007 icozzare@usgs.gov","orcid":"https://orcid.org/0000-0002-5123-1007","contributorId":1693,"corporation":false,"usgs":true,"family":"Cozzarelli","given":"Isabelle","email":"icozzare@usgs.gov","middleInitial":"M.","affiliations":[{"id":436,"text":"National Research Program - Eastern Branch","active":true,"usgs":true},{"id":49175,"text":"Geology, Energy & Minerals Science Center","active":true,"usgs":true}],"preferred":true,"id":397993,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Scholl, Martha A. 0000-0001-6994-4614 mascholl@usgs.gov","orcid":"https://orcid.org/0000-0001-6994-4614","contributorId":1920,"corporation":false,"usgs":true,"family":"Scholl","given":"Martha","email":"mascholl@usgs.gov","middleInitial":"A.","affiliations":[{"id":37277,"text":"WMA - Earth System Processes Division","active":true,"usgs":true}],"preferred":true,"id":397996,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Matthews, L.L.","contributorId":81278,"corporation":false,"usgs":true,"family":"Matthews","given":"L.L.","email":"","affiliations":[],"preferred":false,"id":397995,"contributorType":{"id":1,"text":"Authors"},"rank":4}]}}
,{"id":70023530,"text":"70023530 - 2001 - Spectroscopic evidence for ternary surface complexes in the lead(II)-malonic acid-hematite system","interactions":[],"lastModifiedDate":"2018-12-03T08:43:35","indexId":"70023530","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":2222,"text":"Journal of Colloid and Interface Science","active":true,"publicationSubtype":{"id":10}},"title":"Spectroscopic evidence for ternary surface complexes in the lead(II)-malonic acid-hematite system","docAbstract":"<div id=\"abstracts\" class=\"Abstracts\"><div id=\"aep-abstract-id4\" class=\"abstract author\"><div id=\"aep-abstract-sec-id5\"><p id=\"simple-para0005\">Using extended X-ray absorption fine structure (EXAFS) and attenuated total reflectance Fourier-transform infrared (ATR-FTIR) measurements, we examined the sorption of Pb(II) to hematite in the presence of malonic acid. Pb L<sub>III</sub>-edge EXAFS measurements performed in the presence of malonate indicate the presence of both Fe and C neighbors, suggesting that a major fraction of surface-bound malonate is bonded to adsorbed Pb(II). In the absence of Pb(II), ATR-FTIR measurements of sorbed malonate suggest the formation of more than one malonate surface complex. The dissimilarity of the IR spectrum of malonate sorbed on hematite to those for aqueous malonate suggest at least one of the sorbed malonate species is directly coordinated to surface Fe atoms in an inner-sphere mode. In the presence of Pb, little change is seen in the IR spectrum for sorbed malonate, indicating that geometry of malonate as it coordinates to sorbed Pb(II) adions is similar to the geometry of malonate as it coordinates to Fe in the hematite surface. Fits of the raw EXAFS spectra collected from pH 4 to pH 8 result in average Pb–C distances of 2.98 to 3.14 Å, suggesting the presence of both four- and six-membered Pb–malonate rings. The IR results are consistent with this interpretation. Thus, our results suggest that malonate binds to sorbed Pb(II) adions, forming ternary metal-bridging surface complexes.</p></div></div></div>","language":"English","publisher":"Elsevier","doi":"10.1006/jcis.2000.7345","issn":"00219797","usgsCitation":"Lenhart, J., Bargar, J., and Davis, J., 2001, Spectroscopic evidence for ternary surface complexes in the lead(II)-malonic acid-hematite system: Journal of Colloid and Interface Science, v. 234, no. 2, p. 448-452, https://doi.org/10.1006/jcis.2000.7345.","productDescription":"5 p.","startPage":"448","endPage":"452","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232332,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207407,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1006/jcis.2000.7345"}],"volume":"234","issue":"2","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505b95b0e4b08c986b31b068","contributors":{"authors":[{"text":"Lenhart, J.J.","contributorId":59585,"corporation":false,"usgs":true,"family":"Lenhart","given":"J.J.","email":"","affiliations":[],"preferred":false,"id":397936,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Bargar, J.R.","contributorId":82466,"corporation":false,"usgs":true,"family":"Bargar","given":"J.R.","email":"","affiliations":[],"preferred":false,"id":397938,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Davis, J.A.","contributorId":71694,"corporation":false,"usgs":true,"family":"Davis","given":"J.A.","email":"","affiliations":[],"preferred":false,"id":397937,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023525,"text":"70023525 - 2001 - Assessing an open-well aquifer test in fractured crystalline rock","interactions":[],"lastModifiedDate":"2018-11-30T05:34:49","indexId":"70023525","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":"Assessing an open-well aquifer test in fractured crystalline rock","docAbstract":"Use of open wells to conduct aquifer tests in fractured crystalline rock aquifers is potentially problematic, because open wells can hydraulically connect highly permeable fracture zones at different depths within the rock. Because of this effect, it is questionable whether estimates of the hydraulic properties of the rock obtained from analysis of an open-well aquifer test in fractured crystalline rock are representative of the true rock properties. To address this issue, rock properties estimated from such a test are compared with rock properties estimated from an aquifer test at the same location in which packers were installed in wells to restrict vertical fluid movement along the wellbores. Results indicate that when the open-hole test is analyzed with a numerical model that accurately represents the three-dimensional heterogeneity structure in the wellfield, the open-hole test estimates of the rock hydraulic properties are similar to the packer-isolated test estimates. When the open-well test is analyzed using a model having an oversimplified representation of the rock heterogeneity, the estimates of rock transmissivity are similar to the transmissivity estimates from the packer-isolated test, but the storativity estimates are larger than the storativity estimates from the packer-isolated test. These results indicate the importance of accurately representing the rock heterogeneity structure when analyzing an open-hole aquifer test in fractured crystalline rock.Use of open wells to conduct aquifer tests in fractured crystalline rock aquifers is potentially problematic, because open wells can hydraulically connect highly permeable fracture zones at different depths within the rock. Because of this effect, it is questionable whether estimates of the hydraulic properties of the rock obtained from analysis of an open-well aquifer test in fractured crystalline rock are representative of the true rock properties. To address this issue, rock properties estimated from such a test are compared with rock properties estimated from an aquifer test at the same location in which packers were installed in wells to restrict vertical fluid movement along the wellbores. Results indicate that when the open-hole test is analyzed with a numerical model that accurately represents the three-dimensional heterogeneity structure in the wellfield, the open-hole test estimates of the rock hydraulic properties are similar to the packer-isolated test estimates. When the open-well test is analyzed using a model having an oversimplified representation of the rock heterogeneity, the estimates of rock transmissivity are similar to the transmissivity estimates from the packer-isolated test, but the storativity estimates are larger than the storativity estimates from the packer-isolated test. These results indicate the importance of accurately representing the rock heterogeneity structure when analyzing an open-hole aquifer test in fractured crystalline rock.","language":"English","publisher":"National Ground Water Association","doi":"10.1111/j.1745-6584.2001.tb00352.x","issn":"0017467X","usgsCitation":"Tiedeman, C.R., and Hsieh, P.A., 2001, Assessing an open-well aquifer test in fractured crystalline rock: Ground Water, v. 39, no. 1, p. 68-78, https://doi.org/10.1111/j.1745-6584.2001.tb00352.x.","productDescription":"11 p.","startPage":"68","endPage":"78","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232292,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"country":"United States","state":"New Hampshire","city":"Mirror Lake","geographicExtents":"{\n  \"type\": \"FeatureCollection\",\n  \"features\": [\n    {\n      \"type\": \"Feature\",\n      \"properties\": {},\n      \"geometry\": {\n        \"type\": \"Polygon\",\n        \"coordinates\": [\n          [\n            [\n              -72.037353515625,\n              43.9058083561574\n            ],\n            [\n              -71.4111328125,\n              43.9058083561574\n            ],\n            [\n              -71.4111328125,\n              44.43377984606822\n            ],\n            [\n              -72.037353515625,\n              44.43377984606822\n            ],\n            [\n              -72.037353515625,\n              43.9058083561574\n            ]\n          ]\n        ]\n      }\n    }\n  ]\n}","volume":"39","issue":"1","noUsgsAuthors":false,"publicationDate":"2005-12-13","publicationStatus":"PW","scienceBaseUri":"5059edc9e4b0c8380cd499e2","contributors":{"authors":[{"text":"Tiedeman, C. R.","contributorId":104107,"corporation":false,"usgs":true,"family":"Tiedeman","given":"C.","email":"","middleInitial":"R.","affiliations":[],"preferred":false,"id":397923,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Hsieh, P. A.","contributorId":40596,"corporation":false,"usgs":true,"family":"Hsieh","given":"P.","email":"","middleInitial":"A.","affiliations":[],"preferred":false,"id":397922,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023524,"text":"70023524 - 2001 - Methyl t-Butyl Ether Mineralization in Surface-Water Sediment Microcosms under Denitrifying Conditions","interactions":[],"lastModifiedDate":"2018-12-03T09:24:31","indexId":"70023524","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":850,"text":"Applied and Environmental Microbiology","active":true,"publicationSubtype":{"id":10}},"title":"Methyl t-Butyl Ether Mineralization in Surface-Water Sediment Microcosms under Denitrifying Conditions","docAbstract":"Mineralization of [U-14C] methyl t-butyl ether (MTBE) to 14CO2 without accumulation of t-butyl alcohol (TBA) was observed in surface-water sediment microcosms under denitrifying conditions. Methanogenic activity and limited transformation of MTBE to TBA were observed in the absence of denitrification. Results indicate that bed sediment microorganisms can effectively degrade MTBE to nontoxic products under denitrifying conditions.","language":"English","publisher":"ASM","doi":"10.1128/AEM.67.4.1975-1978.2001","issn":"00992240","usgsCitation":"Bradley, P., Chapelle, F.H., and Landmeyer, J., 2001, Methyl t-Butyl Ether Mineralization in Surface-Water Sediment Microcosms under Denitrifying Conditions: Applied and Environmental Microbiology, v. 67, no. 4, p. 1975-1978, https://doi.org/10.1128/AEM.67.4.1975-1978.2001.","productDescription":"4 p.","startPage":"1975","endPage":"1978","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":478930,"rank":10000,"type":{"id":41,"text":"Open Access External Repository Page"},"url":"https://www.ncbi.nlm.nih.gov/pmc/articles/92824","text":"External Repository"},{"id":232254,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207361,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1128/AEM.67.4.1975-1978.2001"}],"volume":"67","issue":"4","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505a5613e4b0c8380cd6d33d","contributors":{"authors":[{"text":"Bradley, P. M. 0000-0001-7522-8606","orcid":"https://orcid.org/0000-0001-7522-8606","contributorId":29465,"corporation":false,"usgs":true,"family":"Bradley","given":"P. M.","affiliations":[],"preferred":false,"id":397919,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Chapelle, F. H.","contributorId":101697,"corporation":false,"usgs":true,"family":"Chapelle","given":"F.","email":"","middleInitial":"H.","affiliations":[],"preferred":false,"id":397921,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Landmeyer, J. E.","contributorId":91140,"corporation":false,"usgs":true,"family":"Landmeyer","given":"J. E.","affiliations":[],"preferred":false,"id":397920,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023523,"text":"70023523 - 2001 - A partition-limited model for the plant uptake of organic contaminants from soil and water","interactions":[],"lastModifiedDate":"2018-11-30T05:41:03","indexId":"70023523","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":"A partition-limited model for the plant uptake of organic contaminants from soil and water","docAbstract":"<div class=\"hlFld-Abstract\"><div id=\"abstractBox\"><p class=\"articleBody_abstractText\">In dealing with the passive transport of organic contaminants from soils to plants (including crops), a partition-limited model is proposed in which (i) the maximum (equilibrium) concentration of a contaminant in any location in the plant is determined by partition equilibrium with its concentration in the soil interstitial water, which in turn is determined essentially by the concentration in the soil organic matter (SOM) and (ii) the extent of approach to partition equilibrium, as measured by the ratio of the contaminant concentrations in plant water and soil interstitial water, α<sub>pt</sub><span>&nbsp;</span>(≤ 1), depends on the transport rate of the contaminant in soil water into the plant and the volume of soil water solution that is required for the plant contaminant level to reach equilibrium with the external soil-water phase. Through reasonable estimates of plant organic-water compositions and of contaminant partition coefficients with various plant components, the model accounts for calculated values of α<sub>pt</sub><span>&nbsp;</span>in several published crop-contamination studies, including near-equilibrium values (i.e., α<sub>pt</sub><span>&nbsp;</span>≅ 1) for relatively water-soluble contaminants and lower values for much less soluble contaminants; the differences are attributed to the much higher partition coefficients of the less soluble compounds between plant lipids and plant water, which necessitates much larger volumes of the plant water transport for achieving the equilibrium capacities. The model analysis indicates that for plants with high water contents the plant-water phase acts as the major reservoir for highly water-soluble contaminants. By contrast, the lipid in a plant, even at small amounts, is usually the major reservoir for highly water-insoluble contaminants.</p></div></div>","language":"English","publisher":"ACS","doi":"10.1021/es0017561","issn":"0013936X","usgsCitation":"Chiou, C.T., Sheng, G., and Manes, M., 2001, A partition-limited model for the plant uptake of organic contaminants from soil and water: Environmental Science & Technology, v. 35, no. 7, p. 1437-1444, https://doi.org/10.1021/es0017561.","productDescription":"8 p.","startPage":"1437","endPage":"1444","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232253,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207360,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1021/es0017561"}],"volume":"35","issue":"7","noUsgsAuthors":false,"publicationDate":"2001-03-02","publicationStatus":"PW","scienceBaseUri":"5059e4d3e4b0c8380cd46959","contributors":{"authors":[{"text":"Chiou, C. T.","contributorId":97080,"corporation":false,"usgs":true,"family":"Chiou","given":"C.","email":"","middleInitial":"T.","affiliations":[],"preferred":false,"id":397918,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Sheng, G.","contributorId":70961,"corporation":false,"usgs":true,"family":"Sheng","given":"G.","email":"","affiliations":[],"preferred":false,"id":397917,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Manes, M.","contributorId":17390,"corporation":false,"usgs":true,"family":"Manes","given":"M.","email":"","affiliations":[],"preferred":false,"id":397916,"contributorType":{"id":1,"text":"Authors"},"rank":3}]}}
,{"id":70023516,"text":"70023516 - 2001 - Potential artifacts in interpretation of differential breakthrough of colloids and dissolved tracers in the context of transport in a zero-valent iron permeable reactive barrier","interactions":[],"lastModifiedDate":"2018-12-03T09:30:36","indexId":"70023516","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":"Potential artifacts in interpretation of differential breakthrough of colloids and dissolved tracers in the context of transport in a zero-valent iron permeable reactive barrier","docAbstract":"Many published studies have used visual comparison of the timing of peak breakthrough of colloids versus conservative dissolved tracers (hereafter referred to as dissolved tracers or tracers) in subsurface media to determine whether they are advected differently, and to elucidate the mechanisms of differential advection. This purely visual approach of determining differential advection may have artifacts, however, due to the attachment of colloids to subsurface media. The attachment of colloids to subsurface media may shift the colloidal peak breakthrough to earlier times, causing an apparent \"faster\" peak breakthrough of colloids relative to dissolve tracers even though the transport velocities for the colloids and the dissolved tracers may actually be equivalent. In this paper, a peak shift analysis was presented to illustrate the artifacts associated with the purely visual approach in determining differential advection, and to quantify the peak shift due to colloid attachment. This peak shift analysis was described within the context of microsphere and bromide transport within a zero-valent iron (ZVI) permeable reactive barrier (PRB) located in Fry Canyon, Utah. Application of the peak shift analysis to the field microsphere and bromide breakthrough data indicated that differential advection of the microspheres relative to the bromide occurred in the monitoring wells closest to the injection well in the PRB. It was hypothesized that the physical heterogeneity at the grain scale, presumably arising from differences in inter- versus intra-particle porosity, contributed to the differential advection of the microspheres versus the bromide in the PRB. The relative breakthrough (RB) of microspheres at different wells was inversely related to the ionic strength of ground water at these wells, in agreement with numerous studies showing that colloid attachment is directly related to solution ionic strength.","language":"English","publisher":"Wiley","doi":"10.1111/j.1745-6584.2001.tb02471.x","issn":"0017467X","usgsCitation":"Zhang, P., Johnson, W., Piana, M., Fuller, C.C., and Naftz, D.L., 2001, Potential artifacts in interpretation of differential breakthrough of colloids and dissolved tracers in the context of transport in a zero-valent iron permeable reactive barrier: Ground Water, v. 39, no. 6, p. 831-840, https://doi.org/10.1111/j.1745-6584.2001.tb02471.x.","productDescription":"10 p.","startPage":"831","endPage":"840","costCenters":[{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232136,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"39","issue":"6","noUsgsAuthors":false,"publicationDate":"2005-12-13","publicationStatus":"PW","scienceBaseUri":"505a7ebde4b0c8380cd7a703","contributors":{"authors":[{"text":"Zhang, P.","contributorId":92822,"corporation":false,"usgs":true,"family":"Zhang","given":"P.","email":"","affiliations":[],"preferred":false,"id":397901,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Johnson, W.P.","contributorId":43315,"corporation":false,"usgs":true,"family":"Johnson","given":"W.P.","email":"","affiliations":[],"preferred":false,"id":397900,"contributorType":{"id":1,"text":"Authors"},"rank":2},{"text":"Piana, M.J.","contributorId":22940,"corporation":false,"usgs":true,"family":"Piana","given":"M.J.","email":"","affiliations":[],"preferred":false,"id":397897,"contributorType":{"id":1,"text":"Authors"},"rank":3},{"text":"Fuller, C. C.","contributorId":29858,"corporation":false,"usgs":true,"family":"Fuller","given":"C.","email":"","middleInitial":"C.","affiliations":[],"preferred":false,"id":397898,"contributorType":{"id":1,"text":"Authors"},"rank":4},{"text":"Naftz, D. L.","contributorId":40624,"corporation":false,"usgs":true,"family":"Naftz","given":"D.","email":"","middleInitial":"L.","affiliations":[],"preferred":false,"id":397899,"contributorType":{"id":1,"text":"Authors"},"rank":5}]}}
,{"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":70023512,"text":"70023512 - 2001 - Online bibliographic sources in hydrology","interactions":[],"lastModifiedDate":"2016-08-25T12:24:42","indexId":"70023512","displayToPublicDate":"2001-01-01T00:00:00","publicationYear":"2001","noYear":false,"publicationType":{"id":2,"text":"Article"},"publicationSubtype":{"id":10,"text":"Journal Article"},"seriesTitle":{"id":3345,"text":"Science and Technology Libraries","active":true,"publicationSubtype":{"id":10}},"title":"Online bibliographic sources in hydrology","docAbstract":"<p><span>Traditional commercial bibliographic databases and indexes provide some access to hydrology materials produced by the government; however, these sources do not provide comprehensive coverage of relevant hydrologic publications. This paper discusses bibliographic information available from the federal government and state geological surveys, water resources agencies, and depositories. In addition to information in these databases, the paper describes the scope, styles of citing, subject terminology, and the ways these information sources are currently being searched, formally and informally, by hydrologists. Information available from the federal and state agencies and from the state depositories might be missed by limiting searches to commercially distributed databases.</span></p>","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Science and Technology Libraries","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1300/J122v21n03_05","issn":"0194262X","usgsCitation":"Wild, E.C., and Havener, W.M., 2001, Online bibliographic sources in hydrology: Science and Technology Libraries, v. 21, no. 3-4, p. 63-86, https://doi.org/10.1300/J122v21n03_05.","startPage":"63","endPage":"86","numberOfPages":"24","costCenters":[],"links":[{"id":232695,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"21","issue":"3-4","noUsgsAuthors":false,"publicationStatus":"PW","scienceBaseUri":"505a6e40e4b0c8380cd75564","contributors":{"authors":[{"text":"Wild, Emily C. 0000-0001-6157-7629 ecwild@usgs.gov","orcid":"https://orcid.org/0000-0001-6157-7629","contributorId":1810,"corporation":false,"usgs":true,"family":"Wild","given":"Emily","email":"ecwild@usgs.gov","middleInitial":"C.","affiliations":[{"id":5081,"text":"Libraries","active":false,"usgs":true}],"preferred":false,"id":397883,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Havener, W. Michael","contributorId":29996,"corporation":false,"usgs":true,"family":"Havener","given":"W.","email":"","middleInitial":"Michael","affiliations":[],"preferred":false,"id":397882,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023494,"text":"70023494 - 2001 - Identification of alkyl dimethylbenzylammonium surfactants in water samples by solid-phase extraction followed by ion trap LC/MS and LC/MS/MS","interactions":[],"lastModifiedDate":"2021-05-27T18:49:24.646915","indexId":"70023494","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":"Identification of alkyl dimethylbenzylammonium surfactants in water samples by solid-phase extraction followed by ion trap LC/MS and LC/MS/MS","docAbstract":"A novel methodology was developed for the determination of alkyl (C12, C14, and C16) dimethylbenzylammonium chloride (benzalkonium chloride or BAC, Chemical Abstract Service number: 8001-54-5) in water samples. This method is based on solid-phase extraction (SPE) using polymeric cartridges, followed by high-performance liquid chromatography/ion trap mass spectrometry (LC/MS) and tandem mass spectrometry(MS/MS) detection, equipped with an electrospray interface in positive ion mode. Chromatographic separation was achieved for three BAC homologues by using a C18 column and a gradient of acetonitrile/10 millimolar aqueous ammonium formate. Total method recoveries were higher than 71% in different water matrices. The main ions observed by LC/MS were at mass-to-charge ratios (m/z) of 304, 332, and 360, which correspond to the molecular ions of the C12, C14, and C16 alkyl BAC, respectively. The unequivocal structural identification of these compounds in water samples was performed by LC/MS/MS after isolation and subsequent fragmentation of each molecular ion. The main fragmentation observed for the three different homologues corresponded to the loss of the toluyl group in the chemical structure, which leads to the fragment ions at m/z 212, 240, and 268 and a tropylium ion, characteristic of all homologues, at m/z 91. Detection limits for the methodology developed in this work were in the low nanogram-per-liter range. Concentration levels of BAC - ranging from 1.2 to 36.6 micrograms per liter - were found in surface-water samples collected downstream from different wastewater-treatment discharges, thus indicating its input and persistence through the wastewater-treatment process.","language":"English","publisher":"ACS","doi":"10.1021/es001742v","issn":"0013936X","usgsCitation":"Ferrer, I., and Furlong, E., 2001, Identification of alkyl dimethylbenzylammonium surfactants in water samples by solid-phase extraction followed by ion trap LC/MS and LC/MS/MS: Environmental Science & Technology, v. 35, no. 12, p. 2583-2588, https://doi.org/10.1021/es001742v.","productDescription":"6 p.","startPage":"2583","endPage":"2588","costCenters":[{"id":452,"text":"National Water Quality Laboratory","active":true,"usgs":true},{"id":589,"text":"Toxic Substances Hydrology Program","active":true,"usgs":true}],"links":[{"id":232447,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"},{"id":207468,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1021/es001742v"}],"volume":"35","issue":"12","noUsgsAuthors":false,"publicationDate":"2001-05-19","publicationStatus":"PW","scienceBaseUri":"505a3820e4b0c8380cd61454","contributors":{"authors":[{"text":"Ferrer, I.","contributorId":97260,"corporation":false,"usgs":true,"family":"Ferrer","given":"I.","email":"","affiliations":[],"preferred":false,"id":397828,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Furlong, E. T. 0000-0002-7305-4603","orcid":"https://orcid.org/0000-0002-7305-4603","contributorId":98346,"corporation":false,"usgs":true,"family":"Furlong","given":"E. T.","affiliations":[],"preferred":false,"id":397829,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
,{"id":70023483,"text":"70023483 - 2001 - Effects of urbanization on streamflow in the Atlanta area (Georgia, USA): A comparative hydrological approach","interactions":[],"lastModifiedDate":"2012-03-12T17:20:00","indexId":"70023483","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":"Effects of urbanization on streamflow in the Atlanta area (Georgia, USA): A comparative hydrological approach","docAbstract":"For the period from 1958 to 1996, streamflow characteristics of a highly urbanized watershed were compared with less-urbanized and non-urbanized watersheds within a 20 000 km2 region in the vicinity of Atlanta, Georgia: In the Piedmont and Blue Ridge physiographic provinces of the southeastern USA. Water levels in several wells completed in surficial and crystalline-rock aquifers were also evaluated. Data were analysed for seven US Geological Survey (USGS) stream gauges, 17 National Weather Service rain gauges, and five USGS monitoring wells. Annual runoff coefficients (RCs; runoff as a fractional percentage of precipitation) for the urban stream (Peachtree Creek) were not significantly greater than for the less-urbanized watersheds. The RCs for some streams were similar to others and the similar streams were grouped according to location. The RCs decreased from the higher elevation and higher relief watersheds to the lower elevation and lower relief watersheds: Values were 0.54 for the two Blue Ridge streams. 0.37 for the four middle Piedmont streams (near Atlanta), and 0.28 for a southern Piedmont stream. For the 25 largest stormflows, the peak flows for Peachtree Creek were 30% to 100% greater then peak flows for the other stream. The storm recession period for the urban stream was 1-2 days less than that for the other streams and the recession was characterized by a 2-day storm recession constant that was, on average, 40 to 100% greater, i.e. streamflow decreased more rapidly than for the other streams. Baseflow recession constants ranged from 35 to 40% lower for Peachtree Creek than for the other streams; this is attributed to lower evapotranspiration losses, which result in a smaller change in groundwater storage than in the less-urbanized watersheds. Low flow of Peachtree Creek ranged from 25 to 35% less than the other streams, possibly the result of decreased infiltration caused by the more efficient routing of stormwater and the paving of groundwater rechange areas. The timing of daily or monthly groundwater-level fluctuations was similar annually in each well, reflecting the seasonal recharge. Although water-level monitoring only began in the 1980s for the two urban wells, water levels displayed a notable decline compared with non-urban wells since then; this is attributed to decreased groundwater rechange in the urban watersheds due to increased imperviousness and related rapid storm runoff. Copyright ?? 2001 John Wiley & Sons, Ltd.","largerWorkType":{"id":2,"text":"Article"},"largerWorkTitle":"Hydrological Processes","largerWorkSubtype":{"id":10,"text":"Journal Article"},"language":"English","doi":"10.1002/hyp.218","issn":"08856087","usgsCitation":"Rose, S., and Peters, N., 2001, Effects of urbanization on streamflow in the Atlanta area (Georgia, USA): A comparative hydrological approach: Hydrological Processes, v. 15, no. 8, p. 1441-1457, https://doi.org/10.1002/hyp.218.","startPage":"1441","endPage":"1457","numberOfPages":"17","costCenters":[],"links":[{"id":207359,"rank":9999,"type":{"id":10,"text":"Digital Object Identifier"},"url":"https://dx.doi.org/10.1002/hyp.218"},{"id":232252,"rank":0,"type":{"id":24,"text":"Thumbnail"},"url":"https://pubs.usgs.gov/thumbnails/outside_thumb.jpg"}],"volume":"15","issue":"8","noUsgsAuthors":false,"publicationDate":"2001-05-25","publicationStatus":"PW","scienceBaseUri":"505a0829e4b0c8380cd519da","contributors":{"authors":[{"text":"Rose, S.","contributorId":56002,"corporation":false,"usgs":true,"family":"Rose","given":"S.","email":"","affiliations":[],"preferred":false,"id":397794,"contributorType":{"id":1,"text":"Authors"},"rank":1},{"text":"Peters, N.E.","contributorId":33332,"corporation":false,"usgs":true,"family":"Peters","given":"N.E.","email":"","affiliations":[],"preferred":false,"id":397793,"contributorType":{"id":1,"text":"Authors"},"rank":2}]}}
]}