Accelerated remediation of pesticide-contaminated soil with zerovalent iron

High pesticide concentrations in soil from spills or discharges can result in point-source contamination of ground and surface waters. Cost-effective technologies are needed for on-site treatment that meet clean-up goals and restore soil function. Remediation is particularly challenging when a mixture of pesticides is present. Zerovalent iron (Fe0) has been shown to promote reductive dechlorination and nitro group reduction of a wide range of contaminants in soil and water. We employed Fe0 for on-site treatment of soil containing > 1000 mg metolachlor, > 55 mg alachlor, > 64 mg atrazine, > 35 mg pendimethalin, and > 10 mg chlorpyrifos kg(-1). While concentrations were highly variable within the windrowed soil, treatment with 5% (w/w) Fe0 resulted in > 60% destruction of the five pesticides within 90 d and increased to > 90% when 2% (w/w) Al2(SO4)3 was added to the Fe0. GC/MS analysis confirmed dechlorination of metolachlor and alachlor during treatment. Our observations support the use of Fe0 for ex situ treatment of pesticide-contaminated soil.     

Concentrations of Hchs and Ddts in the Tissues of River Dolphins,Platanista Gangetica,From the River Ganges,India

Abstract

Concentrations of HCH and DDT organochlorine insecticide residues were measured in blubber, muscle and oil samples from three specimens of river dolphins, Platanista gangetica, from the River Ganges, India. Concentrations of HCH and DDT ranged from 94 to 289 ng g^?1 and from 1324 to 9388 ng g^?1 on wet wt. basis respectively. Comparisons are made with other aquatic mammals and other studies on river dolphins. P. gangetica appears to exhibit similar patterns of accumulation with age and with ß-HCH and p-p′-DDE being accumulated to higher levels than other HCH isomers and parent DDT and its other metabolites, respectively. These organochlorines may pose a health risk to river dolphin populations that are already showing evidence of environmental stress. Further studies are recommended.     

Origin and Distribution of Suspended Organic Matter As Inferred From Carbon Isotope Composition in A Mediterranean Semi-Enclosed Marine System

Abstract

The origin and distribution of suspended organic matter, the trophic features and the stable carbon isotopic composition of particulate organic carbon (POC) were studied monthly in a Western Mediterranean semi-enclosed basin. Sampling stations were selected as a function of wind-exposure and the degree of vegetation cover and then compared with an adjacent unvegetated site. the predominant vegetation was seagrass (Posidonia oceanica and Cymodocea nodosa) and Caulerpa prolifera. Water samples were analyzed for total suspended matter (inorganic and organic fractions), photosynthetic pigments (chlorophyll-a and phaeopigments), dissolved organic carbon, particulate organic carbon and their isotopic composition. Temperature and salinity were also measured at the same sampling sites within range of Mediterranean limits. the suspended organic matter concentration was 1.77 ± 1.55 mg l^?1; the chlorophyll-a concentration was low (0.35 ± 0.24 μg l^?1); the disolved organic carbon concentration was 2,140 ± 2,010 μg l^?1; the particulate organic carbon concentration was 212 ± 106 μg l^?1 and the isotopic composition was 18.77 ± 2.51%_°. There were significant temporal differences except for phaeopigments, POC and its POC isotopic composition, and there were no spatial differences other than for δ¹³C. This picture highlighted a general seasonal trend and trophical features similar to adjacent sea.

Spatial differences in δ¹³C showed that the source of suspended organic matter was different between stations as that between sources and wind-hydrodynamic constraints. In     

Toxic elements leaching in different soils affected by the spill from the aznalcollar pyrite mine (Sevilla,Spain)

A study has been made of the leaching of Cd, Zn, Pb, Cu, Tl and As in three representative soils of the zone affected by the spill from a pyrite mine in Aznalcollar (Sevilla, Spain) employing packed soil columns. According to the breakthrough and cumulative leaching curves, the relative mobilities of the different toxic elements in the columns are as follows: Tl > Cd > Zn > As > Cu > Pb. The results also show that the soils themselves have a good capacity for immobilizing the soluble fraction of the elements from the spilled mud, this capacity varying as follows: clayey soil with a high carbonate content > clayey soil with a moderate carbonate content > sandy‐clay loam soil with a low carbonate content. The results obtained in the work are a valuable contribution to the necessary assessment of the impact of the toxic spill on underground waters.     

Tessaria absinthioides: a possible bio‐monitor for Cd,Pb, and Cu,in the middle and lower basin of the loa river,North Chile

Some ecotoxic metals such as Cd, Pb, and Cu in Tessaria absinthioides were quantified to study its possible use as a bio‐indicator and/or bio‐monitor of these metals. This plant was chosen for its abundance in the area under study, along Chile and even in southern Latin America. For Cd, Pb, and Cu in all three parts of the plant (leaves, stems and roots) a different concentration pattern in each sampling areas was observed. In sampling areas Coya Sur and La Cascada copper and cadmium concentration decrease in order: leaves > roots > stems. In samples collected in Xalquincha the lowest concentrations of Cd and Pb were observed in stems. A maximum of cadmium concentration (9ug/gd.w. in leaves) was found in samples from La Cascada, a inflow to river Loa in Calama. High concentrations of lead were found in roots and leaves. Collected data demonstrate that the main pathway for cadmium is from ground water via roots into the plant. Some data obtained for lead and copper indicate that the influence of dust particles adsorbed on leaves and stems can be higher than uptake from ground water.     

Exposure of ground water to alachlor,atrazine and metolachlor in maize areas of ribatejo and oeste (Portugal)

In irrigated maize areas of an important Portuguese agricultural area, Ribatejo and Oeste Region, alachlor, atrazine and metolachlor were detected in ground water.

During the study performed from 1996 to 1998 atrazine was the herbicide that showed the highest frequency of detection. In the 177 ground water samples collected 62% were contaminated with atrazine, 30% with alachlor and 12% with metolachlor. All these herbicides were detected both in ground water for human consumption and for irrigation, in some cases above 0.1 ug/L. The maximum levels quantified were 13μg/L for alachlor, 30μg/L for atrazine and 56 μg/L for metolachlor.

Seasonal variation of residues in ground water it is also presented through several examples of studies performed during the period 1991–1999.     

The distribution,metabolism and toxicity of 14c-DDT in model aquarium tanks with fish and sediment simulating a tropical marine environment

Studies conducted on the distribution, fate and metabolism of DDT in a model ecosystem simulating a tropical marine environment of fish, Gobious nudiceps, Lethrinus harak, Gobious keinesis, Gobious nebulosis and white shrimp (Panaeus setiferus), show that DDT concentration in the water decreases rapidly within the first 24?h. Rapid accumulation of the pesticide in the biota also reaches a maximum level in 24?h before gradually declining. The bioaccumulation factors calculated for the fish species (G. keinesis) and white shrimp (P. Setiferus) were 270 and 351, respectively, after 24?h. There was a steady build up of DDT residues in the sediment during the first 24?h which continued to a maximum concentration of 6.66?ng/g in the seawater/fish/sediment ecosystem after 3 weeks and 5.27?ng/g in the seawater/shrimps/sediment ecosystem after 2.7 days. The depuration of the accumulated pesticide was slow with only 54% lost in G. nudiceps within 3 days of exposure in fresh sea water. By contrast, depuration was fast in the white shrimp, which lost 97% of the accumulated pesticide under the same conditions. DDT was found to be toxic to two of the fish species (G. nebulosis and L. harak) and to white shrimp, and the degree of toxicity was dependent on the particular species. The 24?h LC₅₀ at room temperature for the fish species G. nebulosis and white shrimp was found to be 0.011 and 0.116?mg/kg, respectively. These levels are comparable to the ones recorded for the temperate organisms. Degradation of DDT to its primary metabolites, DDE and DDD, was found in all the compartments of the ecosystem with DDE being the major metabolite in the fish, shrimps and sediment, while in seawater, DDD dominated as the major metabolite.     

Speciation analysis of butyltin compounds in sediments of the Theoule harbour (France) by GC/AES

Over the last years, great progress in the research on speciation of butyltins has been made. Many coupling techniques have been successfully developed, with better applications to sediments samples in the environment. Sediments were collected from 1999 to 2000 to elucidate butyltin pollution in Theoule harbour. Most of the analysed samples showed evidence of butyltin compounds. The results show that the concentration of Tributyltin (TBT) was in the range 20–200?µg/kg in March 1999, 20–340?µg/kg in June 1999, 180–1280?µg/kg in July 2000, and 55–820?µg/kg in October 2000. A comparison of the MBT, DBT, and TBT results show that in 1999 the concentrations were in the order TBT?DBT?>?MBT, with some exceptions. The patterns observed in many sediment cores show a great disparity of organotin input concentration among the cores collected during one month and also during two different months, and from one season to the other. This paper provides information on the use of the acetic acid leaching system in the determination of butyltin. The method is applied to evaluate the occurrence of these species in sediments from the Theoule harbour, between 1999 and 2000. In this study, a GC/AES was applied, complemented with acetic acid leaching and monitored using two certified reference materials: PACS-2 reference sediment and BCR 462 (Report EUR 18406 EN, 1998).     

Royal jelly inhibited N-acetylation and metabolism of 2-aminofluorene in human liver tumor cells (J5)

The present study was carried out to evaluate the question of whether or not royal jelly affects N-acetylation and metabolism of 2-aminofluorene (2-AF) in the human liver tumor cell line (J 5). N-acetylation and metabolism of 2-AF in intact J5 cells was determined by using high performance liquid chromatography for the amounts of acetylated and nonacetylated 2-AF and profile of 2-AF metabolism. The results indicated that royal jelly displayed a dose-dependent inhibition of N-acetylation of 2-AF in J5 cells. Royal jelly also decreased the profile of 2-AF metabolites in J5 cells. This report is the first demonstration which showed that royal jelly affects N-acetylation of 2-AF in human liver tumor cells (J5).