Fate and degradation of the chemical warfare agent soman on sands

Soman is one of the most toxic nerve agents of the known chemical warfare agents. There is actually few knowledge on the behavior of soman in the event of an environmental contamination. It is in particular unknown whether soman remains on a given surface, evaporates into air, or degrades. Here, we studied the evaporation of soman deposited on silica sand using a laboratory-sized wind tunnel, thermal desorption, and gas chromatography. We also investigated the degradation of soman on silica sand by ³¹phosphorus solid state magic angle spinning nuclear magnetic resonance and gas chromatography–mass spectrometry. Results show that a drop of soman on silica sand spreads laterally while evaporating. The maximum vapor concentration was found when the spreading of the soman drop was maximum on the surface. Simultaneously, soman was absorbed gradually into the pore of sand and degraded to O-pinacolyl-methylphosphonic acid following a pseudo-first-order rate reaction over weeks. To our best knowledge, this is the first report on the fate of soman in a sandy environment.     

Higher Cd adsorption on biogenic elemental selenium nanoparticles

Cadmium (Cd) is a carcinogenic metal contaminating the environment and ending up in wastewaters. There is therefore a need for improved methods to remove Cd by adsorption. Biogenic elemental selenium nanoparticles have been shown to adsorb Zn, Cu and Hg, but these nanoparticles have not been tested for Cd removal. Here we studied the time-dependency and adsorption isotherm of Cd onto biogenic elemental selenium nanoparticles using batch adsorption experiments. We measured ζ-potential values to assess the stability of nanoparticles loaded with Cd. Results show that the maximum Cd adsorption capacity amounts to 176.8 mg of Cd adsorbed per g of biogenic elemental selenium nanoparticles. The ζ-potential of Cd-loaded nanoparticles became less negative from ?32.7 to ?11.7 mV when exposing nanoparticles to an initial Cd concentration of 92.7 mg L^?1. This is the first study that demonstrates the high Cd uptake capacity of biogenic elemental selenium nanoparticles, of 176.8 mg g^?1, when compared to that of traditional adsorbents such as carboxyl-functionalized activated carbon, of 13.5 mg g^?1. An additional benefit is the easy solid–liquid separation by gravity settling due to coagulation of Cd-loaded biogenic elemental selenium nanoparticles.     

Variations in the elemental compositions of plants,and computer‐aided sampling in ecosystems∗

To obtain comparable results of multi‐element analysis of plant materials by different laboratories, a harmonized sampling procedure for terrestrial and marine ecosystems is essential. The heterogeneous distribution of chemical elements in living organisms is influenced by different biological parameters. These parameters are mainly characterized by genetic predetermination, seasonal changes, edaphic and climatic conditions, and delocalization processes of chemical substances by metabolic activities.

The biological variations of the element content in plants were divided into 5 systematic levels, which are: 1. the plant species; 2. the population; 3. the stand (within an ecosystem); 4. the individual; and 5. the plant compartment. Each of these systematic levels can be related to: 1. genetic variabilities; 2. different climatic, edaphic and anthropogenic influences; 3. microclimatic or microedaphic conditions; 4. age of plants (stage of development), exposure to environmental influences (light, wind, pollution etc.), seasonal changes; and 5. transport and deposition of substances within the different plant compartments (organs, tissues, cells, organelles).

An expert system for random and systematic sampling for multi‐element analysis of environmental materials, such as plants, soils and precipitation is presented. After statistical division of the research area, the program provides advice for contamination‐free collection of environmental samples.     

Positive relationships between phenol oxidase activity and extractable phenolics in estuarine soils

Decomposition of recalcitrant materials such as phenolics is known to play a pivotal role in organic matter decomposition and nutrient cycling in estuaries. The specific goals of this study were to determine temporal and spatial variations of phenol oxidase and phenolics in estuarine soils, and to elucidate controlling factors for phenol oxidase activity. To achieve these goals, phenol oxidase activity and phenolic content were measured in soils developed along the side of an estuary in the Han River, Korea. Soil samples were collected in three locations with different vegetation: mud flats, Zizania-dominated soils, and Salix-dominated soils. Monthly measurements were also made in a Zizania-dominated site over a year period. Phenol oxidase activity varied between 0.00 and 0.28 diqc min^?1 g^?1, whilst phenolic content ranged from 0.0–10.5 μg g^?1. A correlation analysis revealed that phenol oxidase activity exhibited positive correlations with phenolic content in both seasonal and spatial data. The same relationship was found when the data were analysed separately for each site. Unlike peatlands or upland forest soils where negative correlations were often found between phenol oxidase activity and phenolics, substrate induction appears to account for the positive correlation in the present study.     

Numerical and field investigation of enhanced in situ denitrification in a shallow-zone well-to-well recirculation system

This study investigated efficiency of in situ enhanced biological denitrification of nitrate-contaminated groundwater which employs a well-to-well circulation in a shallow zone where oxygen might give an adverse affect on the denitrification processes. The numerical model developed for the efficiency test included sequential aerobic and nitrate-based respiration, multi-Monod kinetics of reactive components, growth and decay of biomass, and denitrification inhibition associated with the presence of oxygen. Moreover, reaction kinetics for production of toxic intermediates such as nitrite and nitrous oxide were also included in the model. The developed model was applied to the analysis of enhanced in situ denitrification using an injection/extraction well pair. To evaluate the relative remediation effectiveness, comparisons were made between a continuous fumarate injection test (CFIT) system and a pulsed fumarate injection test (PFIT) system, where both systems had the same total fumarate mass injected into the aquifer. The PFIT system was preferable to the CFIT system because of the high possibility of occurrence of clogging in the latter case at the injection well, with no other significant advantages found in either the CFIT or the PFIT system. Accordingly, this developed numerical model is useful to predict and evaluate an in situ bioremediation by denitrification in aquifers.     

Photoacoustic infrared spectroscopy for conducting gas tracer tests and measuring water saturations in landfills

Gas tracer tests can be used to determine gas flow patterns within landfills, quantify volatile contaminant residence time, and measure water within refuse. While gas chromatography (GC) has been traditionally used to analyze gas tracers in refuse, photoacoustic spectroscopy (PAS) might allow real-time measurements with reduced personnel costs and greater mobility and ease of use. Laboratory and field experiments were conducted to evaluate the efficacy of PAS for conducting gas tracer tests in landfills. Two tracer gases, difluoromethane (DFM) and sulfur hexafluoride (SF₆), were measured with a commercial PAS instrument. Relative measurement errors were invariant with tracer concentration but influenced by background gas: errors were 1-3% in landfill gas but 4-5% in air. Two partitioning gas tracer tests were conducted in an aerobic landfill, and limits of detection (LODs) were 3-4 times larger for DFM with PAS versus GC due to temporal changes in background signals. While higher LODs can be compensated by injecting larger tracer mass, changes in background signals increased the uncertainty in measured water saturations by up to 25% over comparable GC methods. PAS has distinct advantages over GC with respect to personnel costs and ease of use, although for field applications GC analyses of select samples are recommended to quantify instrument interferences.     

Terpenoids tame aggressors: role of chemicals in stingless bee communal nesting

Social insects aggressively defend their nest and surrounding against non-nestmates, which they recognize by an unfamiliar profile of aliphatic hydrocarbons on the cuticle. Prominent exceptions are communal nest aggregations of stingless bees. Stingless bees (Apidae: Meliponini) are also unique in possessing cuticular terpenes which are derived from tree resins and have not yet been reported for any other insect. We showed experimentally that sesquiterpenes from the body surface of the communal nesting bee Tetragonilla collina reduced aggression in otherwise aggressive bees which did not have sesquiterpenes themselves. In the field, bee species nesting in aggregations with T. collina often lack sesquiterpenes in their own cuticular profiles. These species show little aggression towards T. collina, whereas it can be heavily attacked by non-aggregated species that also possess cuticular sesquiterpenes. We conclude that appeasement by sesquiterpenes represents a novel mechanism to achieve interspecific tolerance in social insects.     

Pilot study of personal, indoor and outdoor exposure to benzene, formaldehyde and acetaldehyde

There is a lack of data for health risk assessment of long term personal exposure to certain ubiquitous air pollutants present particularly in urban atmospheres. The relationship between ambient background concentrations and personal exposure is often unknown. A pilot campaign to measure indoor concentrations, outdoor concentrations and personal exposure to benzene, formaldehyde and acetaldehyde was conducted in a medium sized French town. A strong contribution to total personal exposure was observed from indoor sources, especially for formaldehyde and acetaldehyde, suggesting that indoor sources are dominant for these compounds. For benzene, the average personal exposure exceeded a 10 μgm^?3 limit value, although this was not the case for the ambient background concentration. For formaldehyde, the limit level was also exceeded. Observations suggest that true personal exposure cannot be determined directly from measurements pertaining from fixed ambient background monitoring stations. It is hoped that this will be taken into consideration by the bodies responsible for monitoring air pollution and the future European Air Quality Directive.     

Determinants of homeowners' attitudes to the installation of high-voltage overhead transmission lines

This article deals comprehensively with factors which influence attitudes to the placement of high-voltage overhead transmission lines (HVOTLs). It employs an analytical schema which links the initial stimulus of the power lines' proposal in an area to Background and Socio-economic independent variables and a set of mediating variables. From a survey of 600 residents in three different domiciliary settings in Queensland, Australia, results indicate an absence of positive attitudes and, at best, neutral ones to HVOTL placement. By multinomial logistic regression, the study probes the grounds behind negativity and extreme negativity, uncovering direct links between these attitudes and certain of the variables included in the analytical schema.