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951.
Taylor Alicia A. Tsuji Joyce S. Garry Michael R. McArdle Margaret E. Goodfellow William L. Adams William J. Menzie Charles A. 《Environmental management》2020,65(1):131-159
Environmental Management - Decades of study indicate that copper oral exposures are typically not a human health concern. Ingesting high levels of soluble copper salts can cause acute... 相似文献
952.
Jonathan Thornburg Charles E. Rodes Phillip A. Lawless Ron Williams 《Atmospheric environment (Oxford, England : 1994)》2009,43(28):4251-4258
The Detroit Exposure and Aerosol Research Study (DEARS) provided data to compare outdoor residential coarse particulate matter (PM10–2.5) concentrations in six different areas of Detroit with data from a central monitoring site. Daily and seasonal influences on the spatial distribution of PM10–2.5 during Summer 2006 and Winter 2007 were investigated using data collected with the newly developed coarse particle exposure monitor (CPEM). These data allowed the representativeness of the community monitoring site to be assessed for the greater Detroit metro area. Multiple CPEMs collocated with a dichotomous sampler determined the precision and accuracy of the CPEM PM10–2.5 and PM2.5 data.CPEM PM2.5 concentrations agreed well with the dichotomous sampler data. The slope was 0.97 and the R2 was 0.91. CPEM concentrations had an average 23% negative bias and R2 of 0.81. The directional nature of the CPEM sampling efficiency due to bluff body effects probably caused the negative CPEM concentration bias.PM10–2.5 was observed to vary spatially and temporally across Detroit, reflecting the seasonal impact of local sources. Summer PM10–2.5 was 5 μg m?3 higher in the two industrial areas near downtown than the average concentrations in other areas of Detroit. An area impacted by vehicular traffic had concentrations 8 μg m?3 higher than the average concentrations in other parts of Detroit in the winter due to the suspected suspension of road salt. PM10–2.5 Pearson Correlation Coefficients between monitoring locations varied from 0.03 to 0.76. All summer PM10–2.5 correlations were greater than 0.28 and statistically significant (p-value < 0.05). Winter PM10–2.5 correlations greater than 0.33 were statistically significant (p-value < 0.05). The PM10–2.5 correlations found to be insignificant were associated with the area impacted by mobile sources during the winter. The suspected suspension of road salt from the Southfield Freeway, combined with a very stable atmosphere, caused concentrations to be greater in this area compared to other areas of Detroit. These findings indicated that PM10–2.5, although correlated in some instances, varies sufficiently across a complex urban airshed that that a central monitoring site may not adequately represent the population's exposure to PM10–2.5. 相似文献
953.
The effect of specimen confinement on the determination of the effective diffusion coefficients, D*, for chloride, a non-reactive (non-adsorbing) solute, diffusing in a compacted soil was evaluated. The diffusion tests were performed by placing an acetic acid/sodium acetate buffer solution containing ZnCl2 (pH approximately 4.8) in a reservoir in contact with unconfined and confined specimens of a compacted sand-clay mixture for test durations of 7 or 14 d. The concentrations of chloride in the reservoir were measured as a function of time during the test, as well as a function of depth within the specimen at the end of the test. The resulting concentration distributions were analyzed using two models to Fick's second law for non-reactive solute diffusion in porous media, viz., (1) an analytical model assuming the porosity distribution could be represented by a single, weighted mean porosity and (2) a commercially available model, POLLUTE, that directly accounted for the measured porosity distribution. The D* for unconfined specimens based on the analytical model tended to be overestimated by a factor ranging from 1.13 to 1.59 relative to the D* using POLLUTE, whereas the D* values based on both methods for confined specimens typically were more consistent. In addition, the D* for unconfined specimens was greater than the D* for confined specimens when soil concentrations were used for the analysis, presumably due to the higher porosity for the unconfined specimens relative to the confined specimens. Analyses based on reservoir concentrations were inconsistent and contradictory in some cases, suggesting that the D* values based on soil concentrations were more reliable. 相似文献
954.
Putting humans in ecology: consistency in science and management 总被引:1,自引:0,他引:1
Normal and abnormal levels of human participation in ecosystems can be revealed through the use of macro-ecological patterns. Such patterns also provide consistent and objective guidance that will lead to achieving and maintaining ecosystem health and sustainability. This paper focuses on the consistency of this type of guidance and management. Such management, in sharp contrast to current management practices, ensures that our actions as individuals, institutions, political groups, societies, and as a species are applied consistently across all temporal, spatial, and organizational scales. This approach supplants management of today, where inconsistency results from debate, politics, and legal and religious polarity. Consistency is achieved when human endeavors are guided by natural patterns. Pattern-based management meets long-standing demands for enlightened management that requires humans to participate in complex systems in consistent and sustainable ways. 相似文献
955.
Seasonal variation of heavy metals in ambient air and precipitation at a single site in Washington, DC 总被引:1,自引:0,他引:1
Melaku S Morris V Raghavan D Hosten C 《Environmental pollution (Barking, Essex : 1987)》2008,155(1):88-98
Atmospheric samples of precipitation and ambient air were collected at a single site in Washington, DC, for 7 months (for ambient air samples) and 1 year (for wet deposition samples) and analyzed for arsenic, cadmium, chromium and lead. The ranges of heavy metal concentrations for 6-day wet deposition samples collected over the 1-year period were 0.20-1.3 microg/l, 0.060-5.1 microg/l, 0.062-4.6 microg/l and 0.11-3.2 microg/l for arsenic, cadmium, chromium and lead, respectively, with a precision better than 5% for more than 95% of the measurements. The ranges of heavy metal concentrations for the 6-day ambient air samples were 0.800-15.7 ng/m(3), 1.50-30.0 ng/m(3), 16.8-112 ng/m(3), and 2.90-137 ng/m(3) for arsenic, cadmium, chromium and lead, respectively, with a precision better than 10%. The spread in the heavy metal concentration over the observation period suggests a high seasonal variability for heavy metal content in both ambient air and wet deposition samples. 相似文献
956.
Peltier GL Meyer JL Jagoe CH Hopkins WA 《Environmental pollution (Barking, Essex : 1987)》2008,154(2):283-290
We used the biomonitor, Corbicula fluminea, to investigate the contributions of trace elements associated with different point sources and land uses in a large river. Trace elements were analyzed in tissues of clams collected from 15 tributary streams draining five land use or point source types: agriculture, forest, urban, coal-fired power plant (CFPP), and wastewater (WWTP). Clams from forested catchments had elevated Hg concentrations, and concentrations of arsenic and selenium were highest (5.0+/-0.2 and 13.6+/-0.9 microg g(-1) dry mass (DM), respectively) in clams from CFPP sites. Cadmium concentrations were significantly higher in clams from urban and CFPP sites (4.1+/-0.2 and 3.6+/-0.9 microg g(-1) DM, respectively). Non-metric multidimensional scaling (NMS) of tissue concentrations in clams clustered at CFPP and forest/agriculture sites at opposite ends of the ordination space, and the distribution of sites was driven by Cu, Zn, Cd, and Hg. 相似文献
957.
Han YJ Holsen TM Evers DC Driscoll CT 《Environmental pollution (Barking, Essex : 1987)》2008,156(3):1348-1356
Changes in deposition of gaseous divalent mercury (Hg(II)) and particulate mercury (Hg(p)) in New Hampshire due to changes in local sources from 1996 to 2002 were assessed using the Industrial Source Complex Short Term (ISCST3) model (regional and global sources and Hg atmospheric reactions were not considered). Mercury (Hg) emissions in New Hampshire and adjacent areas decreased significantly (from 1540 to 880 kg yr−1) during this period, and the average annual modeled deposition of total Hg also declined from 17 to 7.0 μg m−2 yr−1 for the same period. In 2002, the maximum amount of Hg deposition was modeled to be in southern New Hampshire, while for 1996 the maximum deposition occurred farther north and east. The ISCST3 was also used to evaluate two future scenarios. The average percent difference in deposition across all cells was 5% for the 50% reduction scenario and 9% for the 90% reduction scenario. 相似文献
958.
Zhang C Yoon H Werth CJ Valocchi AJ Basu NB Jawitz JW 《Journal of contaminant hydrology》2008,102(1-2):49-60
Nonaqueous phase liquid (NAPL) dissolution was studied in three-dimensional (3D) heterogeneous experimental aquifers (25.5 cm x 9 cm x 8.5 cm) with two different longitudinal correlation lengths (2.1 cm and 1.1 cm) and initial spill volumes (22.5 ml and 10.5 ml). Spatial and temporal distributions of NAPL during dissolution were measured using magnetic resonance imaging (MRI). At high NAPL spill volume, average effluent concentrations initially increased during dissolution, as NAPL pools transitioned to NAPL ganglia, and then decreased as the total NAPL-water interfacial area decreased over time. Experimental results were used to test six dissolution models: (i and ii) a one-dimensional (1D) model using either specific NAPL-water interfacial area values estimated from MR images at each time step (i.e., 1D quasi-steady state model), or an empirical mass transfer (Sh') correlation (i.e., 1D transient model), (iii and iv) a multiple analytical source superposition technique (MASST) using either the NAPL distribution determined from MR images at each time step (i.e., MASST steady state model), or the NAPL distribution determined from mass balance calculations (i.e., MASST transient model), (v) an equilibrium streamtube model, and (vi) a 3D grid-scale pool dissolution model (PDM) with a dispersive mass flux term. The 1D quasi-steady state model and 3D PDM captured effluent concentration values most closely, including some concentration fluctuations due to changes in the extent of flow reduction. The 1D transient, MASST steady state and transient, and streamtube models all showed a monotonic decrease in effluent concentration values over time, and the streamtube model was the most computationally efficient. Changes during dissolution of the effective NAPL-water interfacial area estimated from imaging data are similar to changes in effluent concentration values. The 1D steady state model incorporates estimates of the effective NAPL-water interfacial area directly at each time point; the 3D PDM does so indirectly through mass balance and a relative permeability function, which causes reduced water flow through high saturation NAPL regions. Hence, when model accuracy is required, the results indicate that a surrogate of this effective interfacial area is required. Approaches to include this surrogate in the MASST and streamtube models are recommended. 相似文献
959.
We report the ability of nickel-based catalysts to degrade explosives compounds in aqueous solution. Several nickel catalysts completely degraded the explosives, although rates varied. Nearly all of the organic explosive compounds tested, including 2,4,6-trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX), were rapidly degraded to below detection limits by a powdered nickel on an alumina-silicate support (Aldrich nickel catalyst). Perchlorate degradation was minimal (<25%). Degradation of TNT by Aldrich nickel catalyst resulted in apparent first-order kinetics. Significant gaseous 14C was released and collected in an alkaline solution (most likely carbon dioxide) from [14C]RDX and [14C]HMX, indicating heterocyclic ring cleavage. Significant gaseous 14C was not produced from [14C]TNT, but spectrophotometric evidence indicated loss of aromaticity. Degradation occurred in low ionic strength solutions, groundwater, and from pH 3 to pH 9. Degradation of TNT, RDX, and HMX was maintained in flow-through columns of Aldrich nickel catalyst mixed with sand down to a hydraulic retention time of 4h. These data indicate that nickel-based catalysts may be an effective means for remediation of energetics-contaminated groundwater. 相似文献
960.
Chu S Henny CJ Kaiser JL Drouillard KG Haffner GD Letcher RJ 《Environmental pollution (Barking, Essex : 1987)》2007,145(1):374-381
Current-use chlorophenoxy herbicides including 2,4-dichlorophenoxyacetic acid, dicamba, triclopyr, dicamba, dimethyl tetrachloroterephthalate (DCPA or dacthal), and the metabolite of pyrethroids, 3-phenoxybenzoic acid (3-PBA), and the fungicide, chlorothalonil, were investigated in the eggs of osprey (Pandion haliaetus) that were collected from 15 sites from five study areas Puget Sound/Seattle area of Washington State, USA. DCPA differs from acidic chlorophenoxy herbicides, and is not readily hydrolyzed to free acid or acid metabolites, and thus we developed a new method. Of the 12 chlorophenoxy herbicides and chlorothalonil analyzed only DCPA could be quantified at six of these sites (2.0 to 10.3 pg/g fresh weight). However, higher levels (6.9 to 85.5 pg/g fresh weight) of the unexpected DCPA structural isomer, dimethyl tetrachlorophthalate (diMe-TCP) were quantified in eggs from all sites. diMe-TCP concentrations tended to be higher in eggs from the Everett Harbor area. As diMe-TCP is not an industrial product, and not commercially available, the source of diMe-TCP is unclear. Regardless, these findings indicate that DCPA and diMe-TCP can be accumulated in the food chain of fish-eating osprey, and transferred in ovo to eggs, and thus may be of concern to the health of the developing chick and the general reproductive health of this osprey population. 相似文献