Trihalomethane formation potential of filter isolates of electrolyte-extractable soil organic carbon

Certain organic C moieties of soil origin in drinking source waters of Sacramento-San Joaquin Delta (Delta) can react with chlorine to form trihalomethanes (THMs) during the disinfection process. Isolation and characterization of them and quantitation of their THM formation potential (THMFP) is necessary for developing effective strategies to reduce their influxes in Delta waters and for removing them during drinking water treatment. In this study, organic C from two Delta soils was extracted using deionized H(2)O and four Na- or Ca-based electrolytes of varying electrical conductivity values. Extracts were filtered into particulate, colloidal, fine colloidal, and soluble organic C for quantitation and THMFP determination. Results suggested that <1.5% of soil organic C was electrolyte-extractable. The soluble organic C fraction from both soils dominated in quantity and THMFP. Electrolyte effects were cation dependent. Sodium-based electrolytes at either conductivity level did not significantly decrease extractable organic C (EOC) or THMFP compared with deionized H(2)O. In contrast, Ca-based electrolytes reduced EOC and THMFP by >50% even at 1 dS m(-1). Further increase in Ca concentration did not significantly decrease EOC or THMFP. Most reduction in EOC and THMFP by Ca-based electrolytes occurred with the fractions other than the soluble organic C. Results suggested that under natural soil leaching and runoff conditions, the majority of THMFP is associated with organic C of <0.025 mum in diameter. Further molecular characterization of the fractions with high THMFP may help understand the nature of chlorine-reactive organic C from Delta soils.     

Microbial response to heavy metal-polluted soils: community analysis from phospholipid-linked fatty acids and ester-linked fatty acids extracts

Heavy metal pollution of soil is of concern for human health and ecosystem function. The soil microbial community should be a sensitive indicator of metal contamination effects on bioavailability and biogeochemical processes. Simple methods are needed to determine the degree of in situ pollution and effectiveness of remediating metal-contaminated soils. Currently, phospholipid-linked fatty acids (PLFAs) are preferred for microbial profiling but this method is time consuming, whereas direct soil extraction and transesterification of total ester-linked fatty acids (ELFAs) is attractive because of its simplicity. The 1998 mining acid-metal spill of >4000 ha in the Guadiamar watershed (southwestern Spain) provided a unique opportunity to study these two microbial lipid profiling methods. Replicated treatments were set up as nonpolluted, heavy metal polluted and reclaimed, and polluted soils. Inferences from whole community-diversity analysis and correlations of individual fatty acids with metals suggested Cu, Cd, and Zn were the most important in affecting microbial community structure, along with pH. The microbial stress marker, monounsaturated fatty acids, was significantly lower for reclaimed and polluted soil over nonpolluted soils for both PLFA and ELFA extraction. Another stress marker, the monounsaturated to saturated fatty acids ratio, only showed this for the PLFA. The general fungal marker (18:2omega6c), the arbuscule mycorrhizae marker (16:1omega5c), and iso- and anteiso-branched PLFAs (gram positive bacteria) were suppressed with increasing pollution whereas 17:0cy (gram negative bacteria) increased with metal pollution. For both extraction methods, richness and diversity were greater in nonpolluted soils and lowest in polluted soils. The ELFA method was sensitive for reflecting metal pollution on microbial communities and could be suitable for routine use in ecological monitoring and risk assessment programs because of its simplicity and reproducibility.     

Modified Fenton's processes for effective in‐situ chemical oxidation—Laboratory and field evaluation

Fenton's reagent in its conventional form, although effective for contaminant treatment, is impractical from an in‐situ field application perspective due to low pH requirements (i.e., pH 3‐4), and limited reagent mobility when introduced into the subsurface. Modified Fenton's processes that use chelated‐iron catalysts and stabilized hydrogen peroxide have been developed with the goal of promoting effective in‐situ field application under native pH conditions (i.e., pH 5‐7), while extending the longevity of hydrogen peroxide. Laboratory experiments conducted in soil columns packed with organic soil to compare modified Fenton's catalysts with conventional catalysts (acidified iron [II]) indicated superior mobility and sorption characteristics for modified Fenton's catalysts. Furthermore, the acidic pH of a conventional catalyst was buffered to the native soil range, leading to increased iron precipitation/adsorption following permeation through the soil column. The chelates present within the modified Fenton's catalyst showed greater affinity toward iron compared with the native soil and, hence, minimized iron loss through adsorption during the permeation process even at pH 5‐7. Field effectiveness of the modified Fenton's process was demonstrated at a former dry‐cleaning facility located in northeast Florida. Preliminary laboratory‐scale experiments were conducted on soil‐slurry and groundwater samples to test the process efficacy for remediation of chlorinated solvents. Based on successful experimental results that indicated a 94 percent (soil slurry) to 99 percent (groundwater) reduction of cis‐1,2‐DCE, PCE, and TCE, a field‐scale treatment program was initiated utilizing a plurality of dual‐zone direct push injection points installed in a grid fashion throughout the site. Results of treatment indicated a 72 percent reduction in total chlorinated contamination detected in the site groundwater following the first injection event; the reduction increased to 90 percent following the second injection event. © 2002 Wiley Periodicals Inc.     

THE LODGING VELOCITY FOR EMERGENT AQUATIC PLANTS IN OPEN CHANNELS1

ABSTRACT: The growth of aquatic plants in open‐channels has many adverse environmental effects including, but not limited to, impeding the transport of water, hindering navigation, increasing flood elevations, increasing sediment deposition, and degrading water quality. Existing control strategies include physical removal and chemical treatment. Physical removal is only a temporary solution and chemical treatment is unacceptable if the water will be consumed by humans. The hydrodynamic method can wash out the encroached aquatic plants by keeping flow velocity higher than the critical velocity required to bend and rupture (lodge) their stems. This approach is a promising, physically‐based, efficient, economic, and permanent solution for this problem. However, the success of this approach requires the accurate prediction of the critical lodging velocity. This paper presents an analytic study of the lodging velocity for the submerged portion of aquatic plants of narrow leaved emergent stems that are wider at bottom than the top. Based on the principles of engineering materials and the theory of turbulent flow, a semi‐empirical formula is derived for the prediction of the critical lodging velocity. It indicates that the lodging of aquatic plants is controlled not only by flow conditions but also the geometric and mechanical characteristics of the plants. These analytic results provide a satisfactory explanation of the lodging phenomena observed in the field and are verified by the available experimental data.     

THE STRUCTURE AND PRACTICE OF WATER QUALITY TRADING MARKETS1

ABSTRACT: The use of transferable discharge permits in water pollution, what we will call water quality trading (WQT), is rapidly growing in the U.S. This paper reviews the current status of WQT nationally and discusses the structures of the markets that have been formed. Four main structures are observed in such markets: exchanges, bilateral negotiations, clearinghouses, and sole source offsets. The goals of a WQT program are environmental quality and cost effectiveness. In designing a WQT market, policy makers are constrained by legal restrictions and the physical characteristics of the pollution problem. The choices that must be made include how trading will be authorized, monitored and enforced. How these questions are answered will help determine both the extent to which these goals are achieved, and the market structures that can arise. After discussing the characteristics of different market structures, we evaluate how this framework applies in the case of California's Grassland Drainage Area Tradable Loads Program.     

Carbon storage by urban soils in the United States

We used data available from the literature and measurements from Baltimore, Maryland, to (i) assess inter-city variability of soil organic carbon (SOC) pools (1-m depth) of six cities (Atlanta, Baltimore, Boston, Chicago, Oakland, and Syracuse); (ii) calculate the net effect of urban land-use conversion on SOC pools for the same cities; (iii) use the National Land Cover Database to extrapolate total SOC pools for each of the lower 48 U.S. states; and (iv) compare these totals with aboveground totals of carbon storage by trees. Residential soils in Baltimore had SOC densities that were approximately 20 to 34% less than Moscow or Chicago. By contrast, park soils in Baltimore had more than double the SOC density of Hong Kong. Of the six cities, Atlanta and Chicago had the highest and lowest SOC densities per total area, respectively (7.83 and 5.49 kg m(-2)). On a pervious area basis, the SOC densities increased between 8.32 (Oakland) and 10.82 (Atlanta) kg m(-2). In the northeastern United States, Boston and Syracuse had 1.6-fold less SOC post- than in pre-urban development stage. By contrast, cities located in warmer and/or drier climates had slightly higher SOC pools post- than in pre-urban development stage (4 and 6% for Oakland and Chicago, respectively). For the state analysis, aboveground estimates of C density varied from a low of 0.3 (WY) to a high of 5.1 (GA) kg m(-2), while belowground estimates varied from 4.6 (NV) to 12.7 (NH) kg m(-2). The ratio of aboveground to belowground estimates of C storage varied widely with an overall ratio of 2.8. Our results suggest that urban soils have the potential to sequester large amounts of SOC, especially in residential areas where management inputs and the lack of annual soil disturbances create conditions for net increases in SOC. In addition, our analysis suggests the importance of regional variations of land-use and land-cover distributions, especially wetlands, in estimating urban SOC pools.     

Competitive adsorption and desorption of arsenate,vanadate, and molybdate onto the low-cost adsorbent materials alum water treatment sludge and bauxite

When low-cost adsorbents are being used to remove contaminant ions (e.g. arsenate, vanadate, and molybdate) from wastewater, competitive adsorption/desorption are central processes determining their removal efficiency. Competitive adsorption of As, V, and Mo was investigated using equimolar oxyanion concentrations in single, binary, and tertiary combinations in adsorption isotherm and pH envelope studies while desorption of previously adsorbed oxyanions was examined in solutions containing single and binary oxyanion combinations. The low-cost adsorbent materials used were alum water treatment sludge (amorphous hydroxy-Al) and bauxite ore (crystalline Al oxides). Adsorption isotherm and pH envelope studies showed that Mo had only a small effect in decreasing adsorption of As and V but V and As had substantial and similar effects in reducing adsorption of the other. As had a greater effect than V in reducing adsorption of Mo and it was concluded that the affinity of oxyanions for the surfaces of water treatment sludge and bauxite followed the order As > V >> Mo. In 0.3 M NaCl electrolyte, desorption of previously adsorbed oxyanions amounted to 0.3–3.4% for V and As, and 11–20% for Mo. As had approximately four times greater effect than Mo in increasing desorption of V while V had about three times the effect of Mo in increasing desorption of As. Thus, the order of oxyanions in inducing desorption of the other oxyanions (i.e. As on V and As) was the same as that for adsorption selectivity: As > V >> Mo. Water treatment sludge was a more effective adsorbent than bauxite because it had a greater adsorption capacity for all three anions and, in addition, they were held more strongly so desorption in the background electrolyte was proportionately less. It was concluded that at similar molar concentrations, arsenate would tend to reduce adsorption of vanadate as well as displace vanadate already held on adsorbent surfaces while both anions will compete effectively with molybdate. The limiting factor for simultaneous removal of As, V, and Mo from multielement solutions by adsorption will therefore be the removal of Mo.     

Reduction of urban traffic–related particulate matter—leaf trait matters

Environmental Science and Pollution Research - Particulate matter in European cities, especially in urban areas, is mainly from urban road traffic and constitutes a great threat to the health of...     

Inundation influences on bioavailability of phosphorus in managed wetland sediments in agricultural landscapes

Agricultural runoff carries high nutrient loads to receiving waters, contributing to eutrophication. Managed wetlands can be used in integrated management efforts to intercept nutrients before they enter downstream aquatic systems, but detailed information regarding sorption and desorption of P by wetland sediments during typical inundation cycles is lacking. This study seeks to quantify and elucidate how inundation of wetland sediments affects bioavailability of P and contributions of P to downstream systems. A managed wetland cell in Tunica County, Mississippi was subjected to a simulated agricultural runoff event and was monitored for bioavailable phosphorus (water-extractable P [P], Fe-P, and Al-P) of wetland sediments and water level during the runoff event and for 130 d afterward. Inundation varied longitudinally within the wetland, with data supporting significant temporal relationships between inundation and P desorption. Concentrations of P were significantly higher at the site that exhibited variable hydroperiods (100 m) as compared with sites under consistent inundation. This suggests that sites that are inundated for longer periods of time desorb less P immediately to the environment than sites that have periodic or ephemeral inundation. Concentrations of iron oxalate and NaOH-P were significantly higher at the least inundated site as compared with all other sites (F = 5.43; = 0.001) irrespective of time. These results support the hypothesis that increased hydraulic residence time decreases the bioavailability of P in wetland sediments receiving agricultural runoff. This finding suggests that the restoration of wetlands in the mid-southern United States may be hydrologically managed to improve P retention.