Photodegradation of chlorpyrifos with humic acid-bound suspended matter.

Land exploitation in several developing countries, including tropical areas, has caused a rapid change of the landscape, from forest to farms. This has led to an increase of pesticide use and concentration of suspended matter in river waters, which may cause soil erosion of these areas. Humic acid (HA), one of the main components in the soil particulate organic matter, has a positive effect on the photodegradation of organic matter in water; however, the efficiency of HA-bound suspended matter (HABSM) for pesticide photodegradation is not known. The aim of this study is to clarify the effect of HABSM on the photodegradation of chlorpyrifos employed in artificial soil particulate covered with HA. Experiments were carried out in liquid HA phase, with/without HABSM phase and HABSM with additional LHA phase under light. The adsorption procedure of the pesticide on HABSM was also studied. Our results reveal that adsorption takes place within a short time period on HABSM and that photodegradation is successfully achieved. The additional LHA+HABSM phase have not demonstrated any significant effect of HA concentration to photodegradation of chlorpyrifos. For instance, when 2.0mg/L chlorpyrifos was used in the experiments, concentration reductions caused by adsorption, photodegradation under suspended matter and HABSM were found to be 19.3, 17.7, and 61.7% respectively. This finding suggests that HABSM can be considered as a potential catalyst for pesticide photodegradation under sunlight.

Investigation of the effects of hydrogenotrophic denitrification and anammox on the improvement of the quality of the drinking water supply system.

A drinking water supply system operates at Chyasal (in the Kathmandu Valley, Nepal) for purifying the groundwater that has high levels of ammonium nitrogen (NH4-N). However, high NO3-N concentrations were seen in the water after treatment. To further improve the quality of the drinking water, two types of attached growth reactors were developed for the purification system: (i) a hydrogenotrophic denitrification (HD reactor) and (ii) a concurrent reactor with anammox and hydrogenotrophic denitrification (AnHD reactor). For the HD reactor fed by water containing NO3-N, the denitrification efficiency was high (95-98%) for all NO3-N feed rates (20-40 mg/L). The nitrite-nitrogen (NO2-N) and nitrate-nitrogen (NO3-N) concentrations in the effluent were ∼0.5 mg/L. On the other hand, the AnHD reactor fed with water containing NH4-N and NO2-N was operated under varying flow rates of H2(30-70 mL/min) and intermittent supply periods (1-2 h). The efficiency of the anammox process was found to increase with decreasing H2flow rates or with increasing intermittency of the H2supply, while the efficiency of denitrification decreased under these conditions. For the optimal condition of 1.5 h intermittent H2supply, the anammox and denitrification efficiencies of the AnHD reactor reached 80% and 42%, respectively, while the concentrations of both NH4-N and NO2-N in the effluent were <1.0 mg/L, and no NO3-N was detected. From the experimental results, it is clear that both HD and AnHD reactors can function as efficient and critical units of the water purification system.

Performance of intermittent aeration reactor on NH4-N removal from groundwater resources.

To study the effect of intermittent aeration period on ammonium-nitrogen (NH4-N) removal from groundwater resources, synthetic groundwater was prepared and three reactors were operated under different conditions--"reactor A" under continuous aeration, "reactor B" under 6 h intermittent aeration, and "reactor C" under 2 h intermittent aeration. To facilitate denitrification simultaneously with nitrification, "acetate" was added as an external carbon source with step-wise increase from 0.5 to 1.5 C/N ratio, where C stands for total carbon content in the system, and N for NH4-N concentration in the synthetic groundwater. Results show that complete NH4-N removal was obtained in "reactor B" and "reactor C" at 1.3 and 1.5 C/N ratio respectively; and partial NH4-N removal in "reactor A". These results suggest that intermittent aeration at longer interval could enhance the reactor performance on NH4-N removal in terms of efficiency and low external carbon requirement. Because of consumption of internal carbon by the process, less amount of external carbon is required. Further increase in carbon in a form of acetate (1.5 to 2.5 C/N ratios) increases removal rate (represented by reaction rate coefficient (k) of kinetic equation) as well as occurrence of free cells. It suggests that the operating condition at reactor B with 1.3 C/N ratio is more appropriate for long-term operation at a pilot-scale.

Vulnerability of freshwater resources in large and medium Nepalese river basins to environmental change.

This paper discusses vulnerability of freshwater resources in large and medium Nepalese river basins to environmental change based on evaluation of water resource availability and variation, resource development and use, ecological health and management capacity; and compares the situation with selected sub-basins of the Ganges and the Mekong basins in Asia. Results suggest that water resources in the medium river basins are more vulnerable than in the large basins; and Nepalese basins, in general, are more vulnerable than other selected basins in the Asian region. The vulnerability in the Nepalese basins is more related to poor management capacity followed by resources variation and the least to development pressure. The poor management capacity is mainly related to low productivity of water use and the resources stress is related mainly to variation of the resource.

Presence and mobility of arsenic in estuarine wetland soils of the Scheldt estuary (Belgium).

We aimed to assess the presence and availability of arsenic (As) in intertidal marshes of the Scheldt estuary. Arsenic content was determined in soils sampled at 4 sampling depths in 11 marshes, together with other physicochemical characteristics. Subsequently, a greenhouse experiment was set up in which pore water arsenic (As) concentrations were measured 4 times in a 298-day period in 4 marsh soils at different sampling depths (10, 30, 60 and 90 cm) upon adjusting the water table level to 0, 40 and 80 cm below the surface of these soils. The As content in the soil varied significantly with sampling depth and location. Clay and organic matter seem to promote As accumulation in the upper soil layer (0-20 cm below the surface), whereas sulfide precipitation plays a significant role at higher sampling depths (20-100 cm below the surface). The As concentrations in the pore water of the greenhouse experiment often significantly exceeded the Flemish soil sanitation thresholds for groundwater. There were indications that As release is not only affected by the reductive dissolution of Fe/Mn oxides, but also by e.g. a direct reduction of As(V) to As(III). Below the water table, sulfide precipitation seems to lower As mobility when reducing conditions have been sufficiently established. Above the water table, sulfates and bicarbonates induce As release from the solid soil phase to the pore water.

Spatial distribution of arsenic in the intertidal sediments of River Scheldt, Belgium.

A study was carried out to assess the spatial distribution of arsenic in the intertidal sediments of the River Scheldt in Belgium. Sediment samples were collected from different locations along the River Scheldt up to 100 cm depth and analysed for the major physicochemical properties. The study reveals that the arsenic contents in the sediment samples vary in a wide range, from 2.3 to 140.2 mg kg(-1) dry weight. Moreover, the arsenic concentrations are generally below the background concentrations and remediation thresholds of arsenic in Flanders, Belgium. The occurrence of arsenic is found closely related to some physicochemical properties of the sediments. Arsenic has a strong positive correlation with organic matter and clay contents. On the contrary, a negative correlation exists between arsenic, sand and pH. It is recommended to develop and use organic matter control practices for lowering further accumulation of arsenic within the sediments.

Sphingosine 1-phosphate as a major bioactive lysophospholipid that is released from platelets and interacts with endothelial cells.

The serum-borne lysophospholipid mediators sphingosine 1-phosphate (Sph-1-P) and lysophosphatidic acid (LPA) have been shown to be released from activated platelets and to act on endothelial cells. In this study, we employed the repeated lipid extraction (under alkaline and acidic conditions), capable of detecting Sph-1-P, LPA, and possibly structurally similar lysophospholipids, whereby a marked formation of [(32)P]Sph-1-P, but not [(32)P]LPA, was observed in [(32)P]orthophosphate-labeled platelets. Platelet Sph-1-P release, possibly mediated by protein kinase C, was greatly enhanced in the presence of albumin, which formed a complex with Sph-1-P. This finding suggests that platelet Sph-1-P may become accessible to depletion by albumin when its transbilayer movement (flipping) across the plasma membrane is enhanced by protein kinase C. Although human umbilical vein endothelial cells expressed receptors for both Sph-1-P and LPA, Sph-1-P acted much more potently than LPA on the cells in terms of intracellular Ca(++) mobilization, cytoskeletal reorganization, and migration. The results suggest that Sph-1-P, rather than LPA, is a major bioactive lysophospholipid that is released from platelets and interacts with endothelial cells, under the conditions in which critical platelet-endothelial interactions (including thrombosis, angiogenesis, and atherosclerosis) occur. Furthermore, albumin-bound Sph-1-P may account for at least some of the serum biological activities on endothelial cells, which have been ascribed to the effects of albumin-bound LPA, based on the similarities between LPA and serum effects.

Inactivation of coliphage Q beta by potassium ferrate.

The kinetics of inactivation of a bacteriophage by potassium ferrate were studied with the F-specific RNA-coliphage Q beta. Inactivation in phosphate buffer (pH 6, 7 and 8) containing ferrate could be described by Hom's model. The inactivation rate depended on the pH. However, the relative effects of ferrate concentration and exposure time on inactivation were not affected by a change in pH from 6 to 8. In a study of the mechanism by which ferrate inactivated the virus, the efficiency of viral inactivation after ferrate decomposed in buffer was assayed. Inactivation was still effective and still followed Hom's equation after the complete decomposition of ferrate ion; however, the efficiency of that inactivation disappeared when sodium thiosulfate was added, suggesting that long-lived oxidative intermediates capable of viral inactivation were generated during the decomposition of ferrate ions.

Cytoplasmic cleavage during zoosporogenesis in Thraustochytrium sp.: ultrastructure and the effects of colchicine and D2O.

Subplasmalemma microtubules were present in the cleavage furrows during zoosporogenesis in Thraustochytrium sp. The microtubules transversed the furrows but were not at right angles to nor circumferentially arranged in the plane of cleavage. Evidence of microtubule-plasmalemma bridges was found. Colchicine and deuterium oxide inhibited cleavage. The data suggested that microtubules had a motive rather than a structural function.

Herpes-type virus particles associated with a fungus.

A cultutre of the fungus Thraustochytrium, isolated from an estuary, was infected by ani enveloped virus. The nucleocapsid measured 110 nanometers in diameter and containied a core of DNA. The virus replicated in the nucleus. These findings stronigly suggest that the particles are a herpes-type virus.