Element immobilization in refuse incinerator ashes by solidification in glass, ceramic or cement

Incineration of municipal refuse results in the production of massive quantities of fly ash and bottom ash. Toxic elements in the original refuse may be concentrated up to 40-fold in the resultant ash. There is concern that burial of such ash in landfills could result in leaching of these elements downward into groundwater. In this study, refuse ashes were incorporated into glass, ceramic and cement composites to immobilize such toxic elements. The EP Toxicity Test (1986) was used to show that extraction of such elements by simulated acid rain is effectively blocked in these new solid materials.     

3,3′,4,4′-Tetrachlorobiphenyl in human fat and milk samples

Samples of adipose tissue from 7 male persons and 10 samples of human milk were analyzed for 3,3′,4,4′-tetrachlorobiphenyl by HRGC-HRMS. The levels found are in the lower ppt-range on a fat weight basis     

Butyltins in sediments from Boston Harbor, USA

Sediments from 12 sites in Boston Harbor were assayed for butyltins. The highest levels of tributyltin (TBT) were found at sites where commercial or pleasure boats were moored, where ocean going vessels dock, and at a former shipyard. Little or no TBT was detected at sites which do not have a history of significant boating activity. Dibutyltin and monobutyltin were also detected at most sites, indicating that degradation of TBT occurs at these sites.     

The fate of chlorobenzenes and permethrins during anaerobic sewage sludge digestion

Mixed primary sewage sludge was incubated anaerobically with and without azide addition to prevent biological activity. The behaviour of 1,3-, 1,4- and 1,2-dichlorobenzene, 1,3,5-, 1,2,4- and 1,2,3-trichlorobenzene, 1,2,3,4- and 1,2,4,5-tetrachlorobenzene, hexachlorobenzene, and cis- and trans-permethrin was examined to determine their potential removal during anaerobic digestion. All the chlorobenzenes were removed to varying extents over 32 days of incubation, ranging from 25% removal for 1,3,5-trichlorobenzene to 80% removal for 1,4-dichlorobenzene. Biodegradation may have been responsible for the reductions in 1,3- and 1,4-dichlorobenzene and 1,2,4- and 1,2,3-trichlorobenzene as there was no significant removal of these compounds in azide treated sludge. The removal over 32 days of cis- and transpermethrin was 87% and 96% respectively. These removals were attributed to a chemical or physical process.     

Long-term change in the suitability of welsh streams for dippers Cinclus cinclus as a result of acidification and recovery: a modelling study

Using a recognized and widely used hydrochemical model, MAGIC, long-term changes in acidity were simulated at 104 sites in the acid sensitive region of upland Wales. Conditions were modelled in the future (2010) under different reductions in sulphate deposition from 0 to 90% of 1984 values. Chemical output from the model was used to simulate change in the chemical suitability of streams for a species of river bird, the Dipper Cinclus cinclus, known to be affected by acidification According to simulations, only reductions in sulphate deposition by over 50% of 1984 levels prevented decline in the number of streams chemically suitable for Dippers. Greater reductions in deposition in the model permitted some recovery except where conifer forestry occupied acid sensitive catchments. There are several uncertainties with the models in their present form.     

Distribution and bioaccumulation of selenium in aquatic microcosms

Closed-system microcosms were used to study factors affecting the fate of selenium (Se) in aquatic systems. Distribution and bioaccumulation of Se varied among sediment types and Se species. A mixture of dissolved (75)Se species (selenate, selenite and selenomethionine) was sorbed more rapidly to fine-textured, highly organic pond sediments than to sandy riverine sediments. Sulfate did not affect the distribution and bioaccumulation of (75)Se over the range 80-180 mg SO(4) liter(-1). When each Se species was labeled separately, selenomethionine was lost from the water column more rapidly than selenate or selenite. Selenium lost from the water column accumulated primarily in sediments, but volatilization was also an important pathway for loss of Se added as selenomethionine. Loss rates of dissolved Se residues were more rapid than rates reported from mesocosm and field studies, suggesting that sediment: water interactions are more important in microcosms than in larger test systems. Daphnids accumulated highest concentrations of Se, followed by periphyton and macrophytes. Selenium added as selenomethionine was bioaccumulated preferentially compared to that added as selenite or selenate. Organoselenium compounds such as selenomethione may thus contribute disproportionately to Se bioaccumulation and toxicity in aquatic organisms.     

Residues of phosphamidon in rice fields

Thirty-day-old seedlings of rice plants (IR-20 variety) from the nursery were transplanted into experimental plots and after 52 days were sprayed with phosphamidon (Dimecron 85% EC) at two dose-rates (0.38 kg a.i. ha(-1) and 0.76 kg a.i. ha(-1)). Residues of phosphamidon in the plant, soil and water were analysed by GLC, at various time intervals, and were found to decrease steadily up to 15 days. A second application of the pesticide was made on day 113 and grains harvested on day 138. The residue level in the plants was 0.12 microg g(-1) and in the grains 0.04 microg g(-1) with the high dose. This is slightly below the EPA prescribed tolerance level of 0.05 microg g(-1). The residues in both soil and water were very low, 24 h after spraying.     

Ozone-induced changes in CO2 assimilation, O2 evolution and chlorophyll a fluorescence transients in barley

Spring barley (Hordeum vulgare cv. Klaxon) plants, 9 days old, were exposed to 0.05, 0.10 or 0.15 microl litre(-1) ozone (O3) for 12 days. Fumigation was administered for 7 h between 9.00 h and 16.00 h each day. Using conventional IRGA equipment, the carbon dioxide exchange rate (CER) was shown to decrease with increasing concentration of O3 during the exposure period, falling to 60% of the control value at the highest O3 concentration. Transpiration rates and stomatal conductance showed similar trends. Light saturation curves, obtained using a leaf disc oxygen electrode, demonstrated that O3-treated leaves had lower apparent quantum yields (QY) and generally lower rates of O2 evolution at saturating light and CO2 levels. Oscillations in chlorophyll a fluorescence, normally observed in control plants, could not be detected after O3 treatment and could only be restored to some extent by feeding the phosphate sequestering agent D-mannose to the leaves.     

An automated systems for air sampling with annular denuder systems at a remote site

An automated air sampling system has been designed for use with the annular denuder system (ADS). The automated air sampling system allows for accurate measurements of air volume and day-night sampling while preventing the accumulation of moisture within the ADS caused by condensation or cloud events. The sampling system consists of air flow, monitoring and control subsystems. Calibration of the sampling system against a Hoffer turbine flow meter indicated accurate measurement of air flow volumes. Field testing and preliminary data have shown that the sampling system functions well in a remote mountain forest site, and was relatively unaffected by condensation, fog, or cloud events.