Comparison of two polarity measurements of hydrophobic organic matter for the evaluation of water treatment processes: XAD resin and PRAM.

Dissolved organic matter (DOM) is a mixture of thousands of organic molecules wide-ranging in molecular weight, polarity and physicochemical properties. DOM is responsible for multiple water treatment issues such as trihalomethane (THM) formation potential and membrane fouling. Two methods of evaluating the polarity of DOM are being used for water treatment application: a serial XAD resin adsorption method at acid pH and the polarity rapid assessment method (PRAM) by parallel solid phase extraction (SPE) cartridges at natural pH. These two methods have been described by their authors as able to define a hydrophobic fraction though they do so by sorption onto different types of material at different pHs. The first part of this study compared the PRAM and XAD methods and showed that the hydrophobic fractions defined by the two approaches were not correlated. This result highlighted the difficulties in defining fractions as 'hydrophobic material'. It appeared that the sorbents for XAD-8 (an acrylic polymer containing oxygen) at pH <3 and C-18 (a pure hydrocarbon polymer coating on silica particles) at neutral or pH <3 did not retain similar hydrophobic fractions. This hypothesis was verified by fluorescence spectroscopy of the effluent of the XAD-8 resin and PRAM C-18 SPE cartridge. Finally the study concentrated on the use of fluorescence and ultrafiltration methods in series with PRAM to gain more insight into the structure and characteristics of the hydrophobic DOM present in drinking water sources. This evaluation showed that the smaller molecular weight fraction of DOM (<1 kDa) had a higher percentage of hydrophobic character and that the fluorescence-defined aromatic protein fraction was the most hydrophilic.

Fishing, fish consumption and advisory awareness among Louisiana's recreational fishers.

This paper presents results from the first known population-based survey of recreational fishers in Louisiana (n=1774). The ultimate goal of this study was to obtain data in support of the development of regional advisories for a high exposure population with unique seafood consumption patterns. Between July and August of 2008, a survey was mailed to a random sample of licensed recreational fishers to characterize local fishing habits, sportfish consumption, and advisory awareness. Eighty-eight percent of respondents reported eating sportfish. Respondents ate an estimated mean of four fish meals per month, of which, approximately half were sportfish. Over half of all sportfish meals (54%) were caught in the Gulf of Mexico or bordering brackish areas. Sportfish consumption varied by license and gender; and was highest among Sportsman's Paradise license holders (2.8±0.2 meals per month), and males (2.2±0.1 meals per month). The most frequently consumed sportfish species were red drum, speckled trout, catfish, bass, crappie and bream. Advisory awareness rates varied by gender, ethnicity, geographic area, license type, age and education; and were lowest among women (53%), African-Americans (43%), fishers from the southeast of Louisiana (50%), holders of Senior Hunting and Fishing licenses (51%), individuals between 15 and 19 years of age (41%), and individuals with less than a high school education (43%). Results were used to identify ways to optimize monitoring, advisory development and outreach activities.

An evaluation of mercury levels in Louisiana fish: trends and public health issues.

To characterize statewide fish tissue mercury levels in edible finfish the first comprehensive analysis of Louisiana's fish tissue mercury database was conducted. Analyses were based on fifteen years of fish tissue mercury data collected from 368 waterbodies between 1994 and 2008 (n=14,344). The overall objectives of this study were to establish baseline fish tissue mercury levels; and evaluate species-specific temporal and spatial trends in fish tissue mercury levels. Fish tissue mercury levels ranged from 0.001 ppm (the detection limit) to 5.904 ppm for king mackerel; with an overall geometric mean of 0.218 ppm. Ninety-five percent of samples had mercury levels below the FDA's action level of 1.0 ppm for methylmercury in commercial food. Forty-four percent of all samples had mercury levels above the U.S. EPA's methylmercury fish tissue criterion of 0.3 ppm for sportfish. Species of potential concern include cobia, king mackerel, blackfin tuna, greater amberjack, spotted bass, bowfin, largemouth bass and freshwater drum. There was a significant but small decline in statewide length-adjusted largemouth bass mercury levels between 1994-1999 to 2003-2008 (p<0.05). The highest fish mercury levels were observed in Pearl, Calcasieu, Mermentau, Ouachita, Pontchartrain and Sabine basins. Length-adjusted largemouth bass mercury levels were significantly higher in wetlands and rivers/streams vs. lakes; and in wetlands vs. estuaries (p<0.05). Data were analyzed from a public health perspective to make recommendations for optimizing monitoring and outreach.

Evaluation of the impact of fuel hydrocarbons and oxygenates on groundwater resources.

The environmental behavior of fuel oxygenates (other than methyl tert-butyl ether [MTBE]) is poorly understood because few data have been systematically collected and analyzed. This study evaluated the potential for groundwater resource contamination by fuel hydrocarbons (FHCs) and oxygenates (e.g., tert-butyl alcohol [TBA], tertamyl methyl ether [TAME], diisopropyl ether [DIPE], ethyl tert-butyl ether [ETBE], and MTBE) by examining their occurrence, distribution, and spatial extent in groundwater beneath leaking underground fuel tank (LUFT) facilities, focusing on data collected from over 7200 monitoring wells in 868 LUFT sites from the greater Los Angeles, CA, region. Excluding the composite measure total petroleum hydrocarbons as gasoline (TPHG), TBA has the greatestsite maximum (geometric mean) groundwater concentration among the study analytes; therefore, its presence needs to be confirmed at LUFT sites so that specific cleanup strategies can be developed. The alternative ether oxygenates (DIPE, TAME, and ETBE) are less likely to be detected in groundwater beneath LUFT facilities in the area of California studied and when detected are present at lower dissolved concentrations than MTBE, benzene, or TBA. Groundwater plume length was used as an initial indicator of the threat of contamination to drinking water resources. Approximately 500 LUFT sites were randomly selected and analyzed. The results demonstrate MTBE to pose the greatest problem, followed by TBA and benzene. The alternative ether oxygenates were relatively localized and indicated lesser potential for groundwater resource contamination. However, all indications suggest the alternative ether oxygenates would pose groundwater contamination threats similar to MTBE if their scale of usage is expanded. Plume length data suggest that in the absence of a completely new design and construction of the underground storage tank (UST) system, an effective management strategy may involve placing greater emphasis on UST program for ensuring adequate enforcement and compliance with existing UST regulations.

Evaluation of granular activated carbon technology for the removal of methyl tertiary butyl ether (MTBE) from drinking water.

This study evaluated granular activated carbons (GACs) using rapid small-scale column tests (RSSCTs) on methyl tert-butyl ether (MTBE) levels from 20 to 2000 microg/L, with or without the presence of tert-butyl alcohol, benzene, toluene, p-xylene (BTX) in two groundwater (South Lake Tahoe Utility District [Lake Tahoe, CA] and Arcadia Well Field [Santa Monica, CA]) and a surface water source (Lake Perris, CA). Direct comparison between two GACs was made for RSSCTs conducted with surface water from Lake Perris. The impact of natural organic matter on GAC performance was investigated and found to correspond with total organic carbon concentration in the three source waters. Significant reduction in GAC performance for MTBE due to competitive adsorption from soluble fuel components (e.g., BTX) was observed. Little or no difference in GAC usage rate or bed life was detected as the empty-bed contact time is changed from 10 to 20 min for RSSCTs conducted in the two groundwater sources, whereas the RSSCTs conducted in the surface water source exhibited significant increase in GAC usage rate as the empty-bed contact time is decreased from 20 to 10 min. This finding suggests that the higher NOM content of the surface water over the groundwater sources caused a greater competitive-adsorption effect that made more sites on the GAC to be unavailable to MTBE, thus decreasing its rate of adsorption and GAC performance for MTBE. Finally, the impact of differential influent MTBE concentration on GAC performance was demonstrated.