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1.
Sci Total Environ ; 668: 867-880, 2019 Jun 10.
Artículo en Inglés | MEDLINE | ID: mdl-30870754

RESUMEN

In many aquatic environments, municipal wastewater treatment facility (WWTF) effluent discharges influence local hydrologic and chemical connectivity between the surface-water and adjacent alluvial shallow-groundwater systems. Fourmile Creek located in Polk County, Iowa received effluent from the Ankeny WWTF for nearly forty years before it was shut down in November 2013. The decommissioning of the municipal WWTF provided a unique opportunity to characterize the recovery from impacts of treated wastewater discharge on water quality at the surface-water/groundwater interface in a shallow, unconfined alluvial aquifer. Dissolved major element and trace element concentrations in Fourmile Creek surface water, hyporheic-zone water, and shallow, unconfined groundwater were monitored upstream and downstream from the WWTF discharge before and after the shutdown. Multivariate statistical techniques including principal component analysis (PCA) and agglomerative hierarchical clustering (AHC) were used to differentiate source-water contributions, characterize elemental components, and describe surface-water/groundwater interaction dynamics. During the post-closure assessment, there was subsurface attenuation of wastewater constituents including Al, B, Cu, Gd, K, Mo, Na, P, Pb, Sb, and Zn. During the same time, groundwater concentrations increased for As, Ba, Ca, Fe, Mg, Mn, SiO2, Sr, and U and represented a profile characteristic of the shallow alluvial aquifer. Hydrologic conditions transitioned from predominantly wastewater infiltration and hyporheic exchange before the WWTF shutdown, to predominantly discharge of native groundwater. Precipitation-driven streamflow events created fluctuations in the groundwater water-table elevations, resulting in variable contact between the saturated and unsaturated zones within the unconfined, alluvial aquifer and intermittent exposure to constituents stored in the sediments. The inorganic fingerprint of municipal wastewater was flushed relatively quickly (≤19 weeks) from the hyporheic zone indicating that processes like diffusion or sorption/desorption that might extend recovery may not be important for many trace elements in this system.

2.
Water Res ; 44(4): 1062-71, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19822342

RESUMEN

The effects of a dilute (ionic strength=5x10(-3)M) plume of treated sewage, with elevated levels (3.9 mg/L) of dissolved organic carbon (DOC), upon the pH-dependency and magnitude of bacterial transport through an iron-laden, quartz sand aquifer (Cape Cod, MA) were evaluated using sets of replicate, static minicolumns. Compared with uncontaminated groundwater, the plume chemistry diminished bacterial attachment under mildly acidic (pH 5.0-6.5) in-situ conditions, in spite of the 5-fold increase in ionic strength and substantively enhanced attachment under more alkaline conditions. The effects of the hydrophobic neutral and total fractions of the plume DOC; modest concentrations of fulvic and humic acids (1.5 mg/L); linear alkyl benzene sulfonate (LAS) (25 mg/L); Imbentin (200 microg/L), a model nonionic surfactant; sulfate (28 mg/L); and calcium (20 mg/L) varied sharply in response to relatively small changes in pH, although the plume constituents collectively decreased the pH-dependency of bacterial attachment. LAS and other hydrophobic neutrals (collectively representing only approximately 3% of the plume DOC) had a disproportionately large effect upon bacterial attachment, as did the elevated concentrations of sulfate within the plume. The findings further suggest that the roles of organic plume constituents in transport or bacteria through acidic aquifer sediments can be very different than would be predicted from column studies performed at circumneutral pH and that the inorganic constituents within the plume cannot be ignored.


Asunto(s)
Agua Dulce/química , Microbiología del Suelo , Contaminantes del Agua/química , Benzopiranos/análisis , Benzopiranos/química , Calcio/análisis , Calcio/química , Carbono/análisis , Carbono/química , Filtración , Agua Dulce/microbiología , Sustancias Húmicas/análisis , Concentración de Iones de Hidrógeno , Cinética , Concentración Osmolar , Aguas del Alcantarillado/análisis , Aguas del Alcantarillado/química , Aguas del Alcantarillado/microbiología , Dióxido de Silicio/química , Sulfatos/análisis , Sulfatos/química , Tensoactivos/análisis , Tensoactivos/química , Contaminantes del Agua/análisis
3.
Aquat Toxicol ; 86(1): 91-8, 2008 Jan 20.
Artículo en Inglés | MEDLINE | ID: mdl-18023888

RESUMEN

The synthetic organic compound 4-nonylphenol (NP) has been detected in many human-impacted surface waters in North America. In this study, we examined the ability of NP to alter reproductive competence in male fathead minnows after a 28 day flow-through exposure in a range of environmentally relevant concentrations bracketing the U.S. Environmental Protection Agency toxicity-based NP chronic exposure criterion of 6.1 microg NP/L. Exposure to NP at and above the EPA chronic exposure criterion resulted in an induction of plasma vitellogenin (VTG) within 14 days. However, 7 days after the cessation of exposure, VTG concentrations had dropped more than 50% and few males expressed VTG above the detection threshold. All of the morphological endpoints, including gonadosomatic index, hepatosomatic index, secondary sexual characters, and histopathology, were unaltered by all NP treatments. However, when NP-exposed male fish were allowed to compete with control males for access to nest sites and females, most treatments altered the reproductive competence of exposed males. At lower NP concentrations, exposed males out-competed control males, possibly by being primed through the estrogenic NP exposure in a fashion similar to priming by pheromones released from female fathead minnows. At higher NP exposure concentrations, this priming effect was negated by the adverse effects of the exposure and control males out-competed treated males. Results of this study indicate the complexity of endocrine disrupting effects and the need for multiple analysis levels to assess the effects of these compounds on aquatic organisms.


Asunto(s)
Cyprinidae , Exposición a Riesgos Ambientales , Fenoles/toxicidad , Reproducción/efectos de los fármacos , Contaminantes Químicos del Agua/toxicidad , Animales , Femenino , Masculino , Fenoles/análisis , Distribución Aleatoria , Conducta Sexual Animal/efectos de los fármacos , Factores de Tiempo , Vitelogeninas/sangre
4.
Environ Sci Technol ; 35(19): 3869-76, 2001 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-11642446

RESUMEN

The nature and chlorine reactivity of organic constituents in reclaimed water (tertiary-treated municipal wastewater) before, during, and after recharge into groundwater at the Montebello Forebay in Los Angeles County, CA, was the focus of this study. Dissolved organic matter (DOM) in reclaimed water from this site is primarily a mixture of aromatic sulfonates from anionic surfactant degradation, N-acetyl amino sugars and proteins from bacterial activity, and natural fulvic acid, whereas DOM from native groundwaters in the aquifer to which reclaimed water was recharged consists of natural fulvic acids. The hydrophilic neutral N-acetyl amino sugars that constitute 40% of the DOM in reclaimed water are removed during the first 3 m of vertical infiltration in the recharge basin. Groundwater age dating with 3H and 3He isotopes, and determinations of organic and inorganic C isotopes, enabled clear differentiation of recent recharged water from older native groundwater. Phenol structures in natural fulvic acids in DOM isolated from groundwater produced significant trihalomethanes (THM) and total organic halogen (TOX) yields upon chlorination, and these structures also were responsible for the enhanced SUVA and specific fluorescence characteristics relative to DOM in reclaimed water. Aromatic sulfonates and fulvic acids in reclaimed water DOM produced minimal THM and TOX yields.


Asunto(s)
Compuestos de Cloro/química , Eliminación de Residuos Líquidos , Purificación del Agua , Abastecimiento de Agua , Aminoácidos/química , Compuestos de Cloro/análisis , Conservación de los Recursos Naturales , Monitoreo del Ambiente , Halógenos/química , Compuestos Orgánicos/análisis , Contaminantes del Suelo , Trihalometanos/análisis , Trihalometanos/química
5.
J Contam Hydrol ; 51(3-4): 163-78, 2001 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11588824

RESUMEN

In January 1999, wastewater influent and effluent from the pretreatment plant at the Stringfellow hazardous waste disposal site were sampled along with groundwater at six locations along the groundwater contaminant plume. The objectives of this sampling and study were to identify at the compound class level the unidentified 40-60% of wastewater organic contaminants, and to determine what organic compound classes were being removed by the wastewater pretreatment plant, and what organic compound classes persisted during subsurface waste migration. The unidentified organic wastes are primarily chlorinated aromatic sulfonic acids derived from wastes from DDT manufacture. Trace amounts of EDTA and NTA organic complexing agents were discovered along with carboxylate metabolites of the common alkylphenolpolyethoxylate plasticizers and nonionic surfactants. The wastewater pretreatment plant removed most of the aromatic chlorinated sulfonic acids that have hydrophobic neutral properties, but the p-chlorobenzene-sulfonic acid which is the primary waste constituent passed through the pretreatment plant and was discharged in the treated wastewaters transported to an industrial sewer. During migration in groundwater, p-chlorobenzenesulfonic acid is removed by natural remediation processes. Wastewater organic contaminants have decreased 3- to 45-fold in the groundwater from 1985 to 1999 as a result of site remediation and natural remediation processes. The chlorinated aromatic sulfonic acids with hydrophobic neutral properties persist and have migrated into groundwater that underlies the adjacent residential community.


Asunto(s)
Agua Dulce/análisis , Residuos Peligrosos/análisis , Eliminación de Residuos Líquidos/métodos , Contaminantes Químicos del Agua/análisis , Contaminantes Químicos del Agua/clasificación , Contaminación Química del Agua/análisis , California , Fraccionamiento Químico , Espectroscopía de Resonancia Magnética , Espectroscopía Infrarroja Corta , Movimientos del Agua , Contaminación Química del Agua/prevención & control , Purificación del Agua
6.
Environ Sci Technol ; 35(24): 4805-16, 2001 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-11775156

RESUMEN

This investigation into the occurrence, character, and transformation of dissolved organic matter (DOM) in treatment wetlands in the western United States shows that (i) the nature of DOM in the source water has a major influence on transformations that occur during treatment, (ii) the climate factors have a secondary effect on transformations, (iii) the wetlands receiving treated wastewater can produce a net increase in DOM, and (iv) the hierarchical analytical approach used in this study can measure the subtle DOM transformations that occur. As wastewater treatment plant effluent passes through treatment wetlands, the DOM undergoes transformation to become more aromatic and oxygenated. Autochthonous sources are contributed to the DOM, the nature of which is governed by the developmental stage of the wetland system as well as vegetation patterns. Concentrations of specific wastewater-derived organic contaminants such as linear alkylbenzene sulfonate, caffeine, and ethylenediaminetetraacetic acid were significantly attenuated by wetland treatment and were not contributed by internal loading.


Asunto(s)
Carbono/metabolismo , Conservación de los Recursos Naturales/métodos , Agua Dulce/química , Compuestos Orgánicos/metabolismo , Oxígeno/metabolismo , Aguas del Alcantarillado/química , Biodegradación Ambiental , Clima , Interacciones Hidrofóbicas e Hidrofílicas , Espectroscopía de Resonancia Magnética , Oxidación-Reducción , Suelo , Espectroscopía Infrarroja por Transformada de Fourier , Estados Unidos
7.
Environ Sci Technol ; 28(5): 890-7, 1994 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-22191831
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