Gas-phase photolytic production of hydroxyl radicals in an ultraviolet purifier for air and surfaces

We have measured the concentration of hydroxyl radicals (OH) produced in the gas phase by a commercially available purifier for air and surfaces, using the time rate of decay of n-heptane added to an environmental chamber. The hydroxyl generator, an Odorox® BOSS? model, produces the OH through 185-nm photolysis of ambient water vapor. The steady-state concentration of OH produced in the 120 m³ chamber is, with 2σ error bars, (3.25 ± 0.80) × 10⁶ cm^?3. The properties of the hydroxyl generator, in particular the output of the ultraviolet lamps and the air throughput, together with an estimation of the water concentration, were used to predict the amount of OH produced by the device, with no fitted parameters. To relate this calculation to a steady-state concentration, we must estimate the OH loss rate within the chamber owing to reaction with the n-heptane and the 7 ppb of background hydrocarbons that are present. The result is a predicted steady-state concentration in excellent agreement with the measured value. This shows we understand well the processes occurring in the gas phase during operation of this hydroxyl radical purifier.

Implications: Hydroxyl radical air purifiers are used for cleaning both gaseous contaminants, such as volatile organic compounds (VOCs) or hazardous gases, and biological pathogens, both airborne and on surfaces. This is the first chemical kinetic study of such a purifier that creates gas-phase OH by ultraviolet light photolysis of H₂O. It shows that the amount of hydroxyls produced agrees well with nonparameterized calculations using the purifier lamp output and device airflow. These results can be used for designing appropriate remediation strategies.     

Costs and consequences of variation in the size of ruff leks

Summary We studied 13 ruff leks in a small region on the island of Gotland (Sweden) to investigate the effect of lek size on the costs and benefits of lekking for individual males. Male ruffs occur in two behaviourally and morphologically distinct forms, independents (residents plus marginals) and satellites, whose costs and benefits we have assessed separately. These ruff leks had from 1–10 resident (territory-holding) males and were visited daily by satellites, marginals and females from 5–25 May, when most copulations occurred. We used the average number of independent males, counted during censuses taken every 5 min during 2-h observation periods at each lek, as an index of mean lek size. Per independent male, the numbers of both satellites and females increased significantly with mean lek size. Female arrival rate and attendance (total female-minutes) also increased significantly with mean lek size as did the average per capita rate of mating success for resident males (that of satellites was not quite significant). Thus, the dispersion of both of these male categories did not appear to fit an ideal free distribution with respect to mating success. In addition, the number of independent-independent fights per independent and the rate of satellite-resident dyad formation per resident increased significantly with mean lek size. These results suggest that ruffs on larger leks enjoy higher mating success than those on smaller leks but also that costs increase with lek size. We suggest that independent males distribute themselves so as to maximize their own net benefits and that this factor can account for both the occurrence of ruff leks and the variation in their size. Correspondence to: J. Höglund     

Polybrominated diphenyl ethers in influents,suspended particulate matter,sediments, sewage treatment plant and effluents and biota from the Netherlands

Polybrominated diphenyl ethers (PBDEs) have been determined in 133 samples of suspended particulate matter (SPM), sediments, sewage treatment plant (STP) influents and effluents, fish and mussels from various locations in The Netherlands, as a part of a large Dutch national study on estrogenic contaminants in the aquatic environment (LOES project). Some PBBs were also analysed but not found in any of the samples at detectable levels. PBDEs and PBBs were included in this study because indications of long term effects on the balance of endocrine systems were found in the literature. High concentrations of decaBDE (up to 4600 g/kg dry weight) were found in SPM from the Western Scheldt. These levels are possibly related to spillage during use of PBDEs in industries upstream the river Scheldt in Belgium. SPM was identified as an important carrier for higher brominated diphenyl ethers in the aquatic environment. DecaBDE was not found at detectable levels in flounder, bream and mussels. The bioaccumulation of decaBDE in these fish and shellfish samples is apparently limited. Lower brominated PBDE congeners (tetra/penta) were also found in the Western Scheldt as well as in the Rhine delta and the river Meuse, but in much lower concentrations than the decaBDE. In contrast with decaBDE, the tetra and pentaBDEs were found in biota. It was concluded that at least a small part of the PBDE can pass STPs.     

Establishing principal soil quality parameters influencing earthworms in urban soils using bioassays

Potential contamination at ex-industrial sites means that, prior to change of use, it will be necessary to quantify the extent of risks to potential receptors. To assess ecological hazards, it is often suggested to use biological assessment to augment chemical analyses. Here we investigate the potential of a commonly recommended bioassay, the earthworm reproduction test, to assess the status of urban contaminated soils. Sample points at all study sites had contaminant concentrations above the Dutch soil criteria Target Values. In some cases, the relevant Intervention Values were exceeded. Earthworm survival at most points was high, but reproduction differed significantly in soil from separate patches on the same site. When the interrelationships between soil parameters and reproduction were studied, it was not possible to create a good model of site soil toxicity based on single or even multiple chemical measurements of the soils. We thus conclude that chemical analysis alone is not sufficient to characterize soil quality and confirms the value of biological assays for risk assessment of potentially contaminated soils.     

Taxonomy of groundwater quality using multivariate and spatial analyses in the Tuticorin District,Tamil Nadu,India

A holistic appraisal of the quality of groundwater from the Tuticorin District has been conducted using multivariate statistical and spatial analyses. The objectives of the study were to delineate the spatial and temporal variabilities in groundwater quality and to understand its suitability for human uses. A total of 100 groundwater samples were collected and analyzed for major cations and anions during pre-monsoon and post-monsoon. Water quality index rating was calculated to quantify overall water quality for human consumption. The PRM samples exhibit poor quality in greater percentage when compared with POM due to the dilution after rainfall. Correlation, factor analysis, and plot of the factor scores reflect the seawater intrusion and weathering process. The mineral stability diagrams indicated that the groundwater is in equilibrium with kaolinite and Ca-montmorillonite, whereas Gibbs plot showed that the chemical composition of groundwater in both districts is controlled by the natural weathering processes irrespective of seasons. The major water type identified in this study is the Ca²⁺–Mg²⁺–HCO₃ ^? type, which degrades into predominantly Na⁺–Cl^?–SO₄ ^2? more saline groundwater toward the coast.     

Aqueous-phase reactive uptake of dicarbonyls as a source of organic aerosol over eastern North America

We use a global 3-D atmospheric chemistry model (GEOS-Chem) to simulate surface and aircraft measurements of organic carbon (OC) aerosol over eastern North America during summer 2004 (ICARTT aircraft campaign), with the goal of evaluating the potential importance of a new secondary organic aerosol (SOA) formation pathway via irreversible uptake of dicarbonyl gases (glyoxal and methylglyoxal) by aqueous particles. Both dicarbonyls are predominantly produced in the atmosphere by isoprene, with minor contributions from other biogenic and anthropogenic precursors. Dicarbonyl SOA formation is represented by a reactive uptake coefficient γ = 2.9 × 10^?3 and takes place mainly in clouds. Surface measurements of OC aerosol at the IMPROVE network in the eastern U.S. average 2.2 ± 0.7 μg C m^?3 for July–August 2004 with little regional structure. The corresponding model concentration is 2.8 ± 0.8 μg C m^?3, also with little regional structure due to compensating spatial patterns of biogenic, anthropogenic, and fire contributions. Aircraft measurements of water-soluble organic carbon (WSOC) aerosol average 2.2 ± 1.2 μg C m^?3 in the boundary layer (<2 km) and 0.9 ± 0.8 μg C m^?3 in the free troposphere (2–6 km), consistent with the model (2.0 ± 1.2 μg C m^?3 in the boundary layer and 1.1 ± 1.0 μg C m^?3 in the free troposphere). Source attribution for the WSOC aerosol in the model boundary layer is 27% anthropogenic, 18% fire, 28% semi-volatile SOA, and 27% dicarbonyl SOA. In the free troposphere it is 13% anthropogenic, 37% fire, 23% semi-volatile SOA, and 27% dicarbonyl SOA. Inclusion of dicarbonyl SOA doubles the SOA contribution to WSOC aerosol at all altitudes. Observed and simulated correlations of WSOC aerosol with other chemical variables measured aboard the aircraft suggest a major SOA source in the free troposphere compatible with the dicarbonyl mechanism.