Fate of disinfection by-products in groundwater during aquifer storage and recovery with reclaimed water

Knowledge on the behaviour of disinfection by-products (DBPs) during aquifer storage and recovery (ASR) is limited even though this can be an important consideration where recovered waters are used for potable purposes. A reclaimed water ASR trial in an anoxic aquifer in South Australia has provided some of the first quantitative information at field-scale on the fate and transport of trihalomethanes (THMs) and haloacetic acids (HAAs). The results revealed that THM half-lives varied from <1 to 65 days, with persistence of chloroform being highest and bromoform lowest. HAA attenuation was rapid (<1 day). Rates of THM attenuation were shown to be highly dependent on the geochemical environment as evidenced by the 2-5 fold reduction in half-lives at the ASR well which became methanogenic during the storage phase of the trial, as compared to an observation well situated 4 m away, which remained nitrate-reducing. These findings agree with previous laboratory-based studies which also show persistence declining with increased bromination of THMs and reducing redox conditions. Modelling suggests that the chlorinated injectant has sufficient residual chlorine and natural organic matter for substantial increases in THMs to occur within the aquifer, however this is masked in some of the field observations due to concurrent attenuation, particularly for the more rapidly attenuated brominated compounds. The model is based on data taken from water distribution systems and may not be representative for ASR since bromide and ammonia concentrations in the injected water and the possible role of organic carbon in the aquifer were not taken into consideration. During the storage phase DBP formation potentials were reduced as a result of the removal of precursor material despite an increase in the THM formation potential per unit weight of total organic carbon. This suggests that water quality improvements with respect to THMs and HAAs can be achieved through ASR in anoxic aquifers.     

Fate of autumn-applied metolachlor in a clay loam in the northern U.S. Corn Belt

Application of herbicides in autumn is of interest to land managers who seek to reduce the number of field operations during spring in the northern Corn Belt. A limited number of herbicides, however, posses the physical characteristics that are required to minimize loss from soil over winter. This study examined the fate of one of these herbicides, metolachlor, during three consecutive winters (1994-1995, 1995-1996, and 1996-1997) near Morris, MN. Metolachlor was applied to the top 5 cm of a clay loam that was packed into a 1.8-m long plastic pipe. The pipe was then set inside a larger diameter 1.8-m long plastic pipe that was buried vertically in the field. The gap between the pipes was insulated along the sides and sealed at the top; this configuration allowed collection of leachate and extraction of the smaller diameter pipe while the field soil was frozen. The experimental design was replicated thrice with sample date (date that the smaller diameter pipes were extracted from the field) as the main treatment. Pipes were extracted from the field at least twice during winter and sectioned into 2 cm or larger increments. The soil contained within these sections was then analyzed for metolachlor. Downward movement of metolachlor occurred in the soil profile during the autumn, but only in 1995. This movement was likely caused by exclusion during pore ice formation as the soil froze. At the time of complete soil thaw in spring, the majority of metolachlor was still detected in the zone of application (0-5 cm depth). Some metolachlor, however, was detected 1 to 3 cm below the zone of application in all three years. Downward movement during thaw was due primarily to infiltration of snowmelt and rain. Metolachlor was most vulnerable to degradation during spring, but some loss occurred in autumn prior to freeze-up. This study suggests that autumn-applied metolachlor moves little in a repacked clay loam profile during winter. Further studies are warranted in evaluating movement under a range of soil physical properties and management practices.     

Better estimates of soil carbon from geographical data: a revised global approach

Mitigation and Adaptation Strategies for Global Change - Soils hold the largest pool of organic carbon (C) on Earth; yet, soil organic carbon (SOC) reservoirs are not well represented in climate...     

Methodological complexities of product carbon footprinting: a sensitivity analysis of key variables in a developing country context

Product carbon footprinting schemes adopt different analytical methodologies. The calculations can also be affected by limited data availability and uncertainty surrounding the value of key variables. The combination of these factors reduces the validity of comparing carbon footprints between products and countries.We used data from sugar production in Zambia and Mauritius to test how variations in methodology affected the product carbon footprint (PCF). We calculated a PCF according to PAS 2050 and explored the sensitivity of the results to the variation of key variables.Results showed that land use change emissions can dominate PCFs. The largest potential impact came from assuming global worst case data for land use change emissions where a product's origin is unknown (+1900%). The issue of land use change can lead to high carbon footprints for products from developing countries where more natural vegetation is still being converted and data are most lacking. When land use change is not important, variables such as electricity emission factors, capital inputs and loss of soil carbon had significant impacts on the PCF.This analysis highlights the large effect of methodology on PCFs. These results are of particular concern for developing countries where data are scarce and the use of global worst case data may be prescribed. We recommend the development of more precise emission factors for tropical countries and bio-regions, and encourage the transparent use of PCF methodologies, where data sources, uncertainties and variability are explicitly noted.     

Sand and dust storms: underrated natural hazards

Sand and dust storms (SDS) are wind erosion events typically associated with dryland regions, although they can occur in most environments and their impacts are frequently experienced outside drylands because desert dust haze often is transported great distances. SDS represent hazards to society in numerous ways, yet they do not feature prominently in the disasters literature. This paper considers SDS in a hazard context by examining their ramifications in economic, physical, and social terms, with a focus on agriculture, health, transport, utilities, households, and the commercial and manufacturing sector. There are few assessments of the economic consequences of SDS and those studies that have been conducted lack consistency in data collection methods and analysis. SDS do not result in the significant damage to infrastructure usually associated with many disasters, but the cumulative effects on society can be significant because SDS occur more commonly than most other types of natural hazard.     

Fate of disinfection by-products in groundwater during aquifer storage and recovery with reclaimed water

Knowledge on the behaviour of disinfection by-products (DBPs) during aquifer storage and recovery (ASR) is limited even though this can be an important consideration where recovered waters are used for potable purposes. A reclaimed water ASR trial in an anoxic aquifer in South Australia has provided some of the first quantitative information at field-scale on the fate and transport of trihalomethanes (THMs) and haloacetic acids (HAAs). The results revealed that THM half-lives varied from <1 to 65 days, with persistence of chloroform being highest and bromoform lowest. HAA attenuation was rapid (<1 day). Rates of THM attenuation were shown to be highly dependent on the geochemical environment as evidenced by the 2-5 fold reduction in half-lives at the ASR well which became methanogenic during the storage phase of the trial, as compared to an observation well situated 4 m away, which remained nitrate-reducing. These findings agree with previous laboratory-based studies which also show persistence declining with increased bromination of THMs and reducing redox conditions. Modelling suggests that the chlorinated injectant has sufficient residual chlorine and natural organic matter for substantial increases in THMs to occur within the aquifer, however this is masked in some of the field observations due to concurrent attenuation, particularly for the more rapidly attenuated brominated compounds. The model is based on data taken from water distribution systems and may not be representative for ASR since bromide and ammonia concentrations in the injected water and the possible role of organic carbon in the aquifer were not taken into consideration. During the storage phase DBP formation potentials were reduced as a result of the removal of precursor material despite an increase in the THM formation potential per unit weight of total organic carbon. This suggests that water quality improvements with respect to THMs and HAAs can be achieved through ASR in anoxic aquifers.     

Bromide levels in natural waters: its relationship to levels of both chloride and total dissolved solids and the implications for water treatment

South Australian freshwaters from a wide variety of environments were analysed for bromide and the results correlated with both chloride and total dissolved solids (TDS) concentrations. A linear relationship was obtained which allows chloride data to be successfully used to estimate bromide concentrations. Bromide displayed a slightly better correlation with TDS indicating that an improved estimate of bromide could be made by reference to TDS data which is more easily and commonly obtained, and generally available extensively as historical data. The bromide content in relation to its ratio with both chloride and TDS contents was around seventy percent of the corresponding ratios found in seawater, a finding reported in other published data. The ability to estimate bromide concentrations is a potentially useful tool in the drinking water industry as it enables the assessment of the extent of bromate formation (predicted through the use of mathematical models and other water quality data) which is an important factor when ozonation is being considered as a treatment option, particularly as many water industry regulatory bodies have imposed stringent limits on the levels of acceptable bromate.