Detection of indoor PCB contamination by thermal desorption of dust. A rapid screening method?

Although PCB in caulking materials has been forbidden for many years in most of Europe, including Denmark, there has been continued interest to measure PCB levels in the air of contaminated buildings and blood of the occupants (Mengon and Schlatter 1993, Fromme et al. 1996, Ewers et al. 1998, Currado and Harrad 1998, Gabrio et al. 2000). The relatively low priority for investigations of this contamination is probably due to the small quantities inhaled compared to exposure via food, and the rapid metabolism of the most volatile congeners demonstrated by low concentrations of all congeners in the blood of exposed persons (Ewers et al. 1998, Gabrio et al. 2000). There is, however, evidence that PCB containing caulking materials have been used even during the '90s (Fromme et al. 1996). In Denmark, it is estimated that 75 t PCB is still in buildings (Organization of Sealant Branch's Manufacturers and Distributors 2000). During an investigation of dust from buildings with excessive microbial growth (including 35 rooms from 9 buildings), the analysis of semivolatile compounds by thermal desorption-GC/MS of samples from a single building surprisingly revealed large amounts of PCBs containing 3, 4 and 5 chlorine atoms, 10-20 times the amounts found in samples from other buildings. Extraction of the dust by SFE followed by GC/ECD analysis for 12 PCB congeners showed that there was approximately 20 times the total PCB concentrations in dust from the polluted building compared to the levels in the other buildings. Subsequent headspace analysis of caulking material from the polluted building revealed this to be the source. Shelf dust functions as a passive sampling medium and, thus, can be used as a screening method to detect PCB and other semivolatile pollution indoors.     

Fate and potential environmental effects of methylenediphenyl diisocyanate and toluene diisocyanate released into the atmosphere

Information from a variety of sources has been collected and summarized to facilitate an overview of the atmospheric fate and potential environmental effects of emissions of methylenediphenyl diisocyanate (MDI) or toluene diisocyanate (TDI) to the atmosphere. Atmospheric emissions of both MDI and TDI are low, both in terms of concentration and mass, because of their low volatility and the need for careful control over all aspects of their lifecycle from manufacture through disposal. Typical emission losses for TDI are 25 g/t of TDI used in slabstock foam production. MDI emission losses are lower, often less than 1 g/t of MDI used. Dispersion modeling predicts that concentrations at the fenceline or beyond are very low for typical releases. Laboratory studies show that TDI (and by analogy MDI) does not react with water in the gas phase at a significant rate. The primary degradation reaction of these aromatic diisocyanates in the atmosphere is expected to be oxidation by OH radicals with an estimated half-life of one day. Laboratory studies also show that this reaction is not expected to result in increased ground-level ozone accumulation.     

Comparison of two methods for estimation of soil sorption for imidacloprid and carbofuran

Predicting the fate and transport of pesticides in soil environment is an important issue especially in understanding and modelling of the environmental behaviour of pesticides. Classical batch sorption method often has been identified as insufficient to derive the actual extent of sorption. In this study, the batch equilibrium method was compared to the centrifugation method, which can permit measurement of sorption under more natural conditions. The results of the comparison of the batch with the centrifugation method for imidacloprid and carbofuran pesticides indicate that the batch method overestimates sorption in comparison to the centrifugation method. These results are in agreement with others, which use high soil:solution ratios with batch and those that used the centrifugation method.     

Preliminary evidence that copper inhibits the degradation of DDT to DDE in pip and stonefruit orchard soils in the Auckland region,New Zealand

Orchards (n=13) were sampled as part of a larger survey investigating agrichemical residues (pesticides and trace elements) in cropping soils in the Auckland region, New Zealand. SigmaDDT concentrations in orchard soils ranged from <0.03 to 24.41 mg kg(-1). DDT (o,p'- and p,p'-) comprised at least 40% of the SigmaDDT residues in 67% of orchards in which DDT residues were detected. There was a highly significant negative correlation (-0.924, P<0.001) between copper concentration (21-490 mg kg-1) and the ratio of DDE:DDT (0.4-5.2) in pip and stonefruit orchard soils. In further investigations involving five pip and stone fruit orchard sites and one grazing paddock it was found that soil respiration and the ratio of soil microbial carbon to soil carbon (%Cmic/Org-C) in orchard soils decreased with increasing copper concentration. These findings are consistent with the conclusion that elevated soil copper concentrations in pip and stone fruit orchard soils in the Auckland region may have reduced the ability of the indigenous soil microbial community to degrade DDT to DDE     

Toxicity and bioaccumulation of reduced TNT metabolites in the earthworm Eisenia andrei exposed to amended forest soil

Soils contaminated with 2,4,6-trinitrotoluene (TNT) and TNT primary reduction products have been found to be toxic to certain soil invertebrates, such as earthworms. The mechanism of toxicity of TNT and of its by-products is still not known. To ascertain if one of the TNT reduction products underlies TNT toxicity, we tested the toxicity and bioaccumulation of TNT reduction products. 2-Amino-4,6-dinitrotoluene (2-ADNT), 4-amino-2,6-dinitrotoluene (4-ADNT), 2,4-diamino-6-nitrotoluene (2,4-DANT) and 2,6-diamino-4-nitrotoluene (2,6-DANT) were tested separately in adult earthworms (Eisenia andrei) following a 14-d exposure to amended sandy loam forest soil. TNT, 4-ADNT, and 2-ADNT were lethal to earthworms (14-d LC(50) were: 580, 531 and 1088 micromol kg(-1), or 132, 105 and 215 mgkg(-1) dry soil, respectively) and gave the following order of toxicity: 4-ADNT>TNT>2-ADNT. Exposure to 2,4-DANT and to 2,6-DANT caused no mortality at 600 micromol kg(-1) or 100 mgkg(-1) dry soil. We found that all four TNT reduction products accumulated in earthworm tissues and 2-ADNT reached the highest levels at 3.0+/-0.3 micromol g(-1) tissue. The 14-d bioaccumulation factors were 5.1, 6.4, 5.1 and 3.2 for 2-ADNT, 4-ADNT, 2,4-DANT and 2,6-DANT, respectively. Results also suggest that some TNT metabolites are at least as toxic as TNT and should be considered when evaluating the overall toxicity of TNT-contaminated soil to earthworms.     

Multiphase flow and transport through fractured heterogeneous porous media

The migration of Dense, Non-Aqueous Phase Liquid (DNAPL) and dissolved phase contamination through a fractured heterogeneous porous medium has been investigated through the use of a multiphase compositional model. The sensitivity of the timescales of migration and the distribution of contaminant in the subsurface to the mean permeability, the variance of the permeability, and the degree of fracturing of the domain were examined. It was found that increasing the mean permeability of the domain allowed the DNAPL to penetrate deeper into the subsurface, while decreasing the mean permeability caused the DNAPL to pool at shallower depths. The presence of fractures within the system was found to control the infiltration only in the most fractured domain. Moment analysis of the nonwetting phase showed that large-scale movement had ceased after approximately 9 years (maximum duration of the source-on condition was approximately 4.5 years). This tended to be due to a redistribution of the DNAPL towards a residual configuration, as was evidenced by the gradual trending of average nonwetting phase saturations within the domain to a static value. The dissolved phase plume was found to migrate at essentially the same rate as the nonwetting phase, due to the reduced relative permeability of lenses containing DNAPL, and due to diffusive losses of mass to the matrix of fractured clay and silty-clay lenses. Some exceptions to this were found when the DNAPL could not overcome the displacement pressure of a lens, and could not by-pass the lens due to the lack of available driving force after the source had been shut off.     

Spatial and temporal shifts in stable isotope values of the bottom-dwelling shrimp<Emphasis Type="Italic"> Nauticaris marionis</Emphasis> at the sub-Antarctic archipelago

Spatial and temporal dynamics of carbon and nitrogen stable isotope signatures of the bottom-dwelling caridean shrimp Nauticaris marionis were measured during April and May between 1984 and 2000 in the vicinity of Marion Island (the Prince Edward Islands, Southern Ocean). There was one trophic-level enrichment in bulk ¹⁵N and ¹³C signatures between small (<20 mm long) and large (>20 mm) specimens of N. marionis, suggesting distinct trophic differentiation among major shrimp size groups. Both ¹⁵N and ¹³C values of N. marionis increased with the depth, reflecting changes in their diet. There were no clear temporal trends in bulk ¹⁵N signatures of N. marionis. However, compound-specific ¹⁵N measurements of amino acids indicated that N. marionis from the inter-island realm occupied the trophic level of second order carnivores, while similarly sized shrimps in the near-shore realm were at the trophic level of first order carnivores. Compound-specific measurements also identified a change in the source of inorganic nitrogen at the base of the food web between the inter-island and near-shore realms. In contrast to the bulk ¹⁵N values, a significant shift in bulk ¹³C values of N. marionis was observed between 1984 and more recent years. This temporal change appears to be linked to changes in the overall productivity of the Prince Edward Island inter-island system, which could be linked to global climate change.Communicated by J.P. Thorpe, Port Erin     

Genetic variability in littoral gastropods: Phosphoglucose isomerase and phosphoglucomutase in Patella vulgata and P. aspera

Genetic variability of the phosphoglucose isomerase (PGI) and phosphoglucomutase (PGM) loci are compared in Patella vulgata L. and P. aspera Lamark from two sites on the west and south coasts of Ireland. P. vulgata was less variable than P. aspera at these 2 loci, and in only 1 of 7 other loci briefly examined was P. vulgata more variable. Evidence is also presented that the PGI enzyme in P. vulgata is more stable at high temperature than that of P aspera. The significance of these observations is discussed in the light of, the different zonal distributions of these species on the shore.     

The Presence of Calcium Oxalate Dihydrate (Weddellite) in Street Sediments from Niterói, Brazil and Its Health Implications

Established research in first world urban environments has shown street sediments to be effective sinks for heavy metals and emphasises the health risks to children by its inhalation or ingestion. In third world countries with fewer pollution controls, contamination may be augmented by additional pollutants such as sewage discharge into urban streets and/or periodic inundation with sewage-laden run-off. This pollutant not only contains heavy metals and organic matter, but calcium oxalates that may derive directly from the sewage itself. To study this premise street sediments were collected from sites of varying industrialisation and sewage contamination within the city of Niteroi, Brazil. Calcium oxalate dihydrate (weddellite) was identified by X-ray diffraction, fourier transform infra red and scanning electron microscopy techniques and oxalate concentrations in <63m and colloidal (clay and organic matter) fractions, were determined by ion chromatography. Oxalate in colloidal fractions averaged 43601mgkg^–1 in sewage contaminated industrialised urban zones, 4519mgkg^–1 in suburban areas and 17477mgkg^–1 in suburbs with favelas (shantytowns-of Niterói). Oxalate concentrations coincide with high levels of metal ions (Fe, Mn, Zn, Pb, Ni, Cr) that stabilise calcium oxalate dihydrate and prevent its dehydration to the monohydrate (whewellite). Lower levels of oxalate were found in lichen-covered roof sediment, plaster and mortar samples. Oxalate concentration coincides with sewage contamination and street sediments appear to act as a sink for calcium oxalate dihydrate derived from sewage. Previous studies have shown that low levels of exposure can damage kidneys and the nervous system, while prolonged exposure can cause severe corneal, retinal and skin damage, cyanosis and possibly gangrene. Contact with blood serum may result in hypocalcemia, muscular stimulation, convulsions and finally collapse. The conditions described are common throughout urban areas of the developing world and may suggest a particular environmental hazard in these regions.