Estimating middle-, neighborhood-, and urban-scale contributions to elemental carbon in Mexico City with a rapid response aethalometer.

A successive moving average subtraction method is developed and applied to black carbon measured over 5-min intervals at a downtown location near many small emitters and at a suburban residential site within the urban plume but distant from specific emitters. Short-duration pulses assumed to originate from nearby sources are subtracted from the concentrations at each site and are summed to estimate middle-scale (approximately 0.1-1 km) contributions. The difference of the remaining baselines at the urban and suburban monitors is interpreted as the contribution to the downtown monitor from source emissions mixed over a neighborhood scale (1-5 km). The baseline at the suburban site is interpreted as the contribution of the mixture of black carbon sources for the entire city. When applied to a 24-day period from February and March 1997 in Mexico City, the analysis showed that 65% of the 24-hr black carbon was part of the urban mixture, 23% originated in the neighborhood surrounding the monitor, and only 12% was contributed from nearby sources. These analyses indicate that a fixed-site monitor can reasonably represent exposures in its surrounding neighborhood even when many local sources, such as exhaust from diesel buses and trucks, affect the monitor.     

Dry deposition and particle size distributions of nitrate and sulfate in ambient air

This study reports the dry deposition pollutants of anion species (NO₃ ^‐ and SO₄ ^‐2) in the Ping Tung City of Southern Taiwan. Several deposition properties are discussed in this paper. It included dry deposition flux, anion species size distribution and deposition velocities. Noll Rotary Impactor (NRI) and Microorifice Uniform Deposit Impactor (MOUDI) were used to collect ambient air coarse and fine particulate. Dry deposition plate was applied to collect particle deposition flux. Dionex 2000i/SP Ion Chromatography equipped with 4 mm AG4A‐SC and AS4A‐SC column was employed to analyze the anion species. The eluent solution is 1.8 mM sodium carbonate/1.7 mM sodium bicarbonate. The measured dry deposition flux of nitrate ranged from 0.63 to 3.96 mg/m²‐day and averaged 2.12 mg/m²‐day, while the measured dry deposition of sulfate ranged from 1.17 to 9.53 mg/m²‐day and averaged 3.92 mg/m²‐day. The particle size distribution of nitrate has bimodal particle size distributions. However, the sulfate displayed uniform particle size distribution for all four sampling sites. Mean cumulative fraction (F%) of nitrate in the particle size range below 1, 2.5, 10 and 25 μm, in sequence, were 34.6%, 60.9%, 91.0% and 97.6%, respectively. However, the mean F% of sulfate in the particle size range below 1, 2.5, 10 and 25 um, in sequence, were 57.3%, 82.6%, 90.3% and 98.0%, respectively. The sulfate has more F% in the submicron particles. The mean MMD _o of nitrate and sulfate are 2.35 and 0.87 μm, respectively. The mean dry deposition velocities of nitrate and sulfate are 0.45 and 0.38 cm/sec, respectively.     

Trace analysis of airborne toluene diisocyanate as a pentafluorobenzyl derivative by gas chromatography with electron capture detection

Trace analysis of airborne toluene diisocyanate (TDI) vapor was accomplished by measuring the derivative using gas chromatography with electron‐capture detector after collecting gas samples with a microimpinger containing 2 ml toluene, 1 μl pentafluorobenzyl alcohol, and 1 μl triethylamine. The sampling efficiency was determined to be 99.4% for short‐term exposure level of TDI and the 2,4‐ and 2,6‐isomers of TDI were well separated. The derivative was identified to be a new compound with a molecular weight of 570 by mass spectrometry in fast atomic bombardment mode and nuclear magnetic resonance spectrometry. This method is convenient and can be applied in the field where airborne TDI is in vapor form.     

Effects of Modified Starch and Different Molecular Weight Polyvinyl Alcohols on Biodegradable Characteristics of Polyvinyl Alcohol/Starch Blends

The common biodegradable properties of polymer make them an excellent pair for blending, and the water solubility of polyvinyl alcohol (PVA) makes it easy to mix evenly with the starch. In this study, PVAs with different molecular weights were blended with various compositions of cross-linked starch (CLS) to explore the effects of molecular weight of PVA on the biodegradable characteristics of the PVA/starch blends. Comparing the biodegradability of all the various PVA/starch blends, a PVA was singled out from the PVA/starch blends of higher biodegradability. Further, the chosen PVA was then blended with the acid-modified starch (AMS) to systematically investigate the effects of the modified processing of starch on the biodegradable characteristics of the PVA/starch blends. Differential scanning calorimetry (DSC) analysis of PVA and PVA/starch specimens reveal that the T_m values of PVA/starch specimens reduce gradually as their CLS or AMS contents increase. After the CLS is blended in PVAs of different molecular weights, the tensile strength (??_f) and elongation at break (??_f) values of (P₁₀₀S₀)G₂₀M₁ specimen increase and simultaneously reduce, respectively, as their molecular weights of PVA increase from about 80,000 (PVA_BF-17) to 120,000 (PVA_BF-26). The ??_f and ??_f values of the PVA/modified-starch blends decrease with an increase in the modified starch contents. The ??_f values of the PVA/AMS specimens decrease with an increase in the concentrations of hydrochloric acid. Comparing the ??_f values of the PVA/CLS specimens with those of the PVA/AMS specimens, the ??_f values of the PVA/CLS specimens are better than those of the PVA/AMS specimens. On the contrary, the ??_f values of the PVA/AMS specimens are better than those of the PVA/CLS specimens. According to the biodegradability of all the PVA/starch blends, PVA with higher molecular weights displays higher biodegradability. The biodegradability of the PVA/modified-starch blends increase as the modified starch contents of the PVA/modified-starch blends increase. As evidenced by the results of the biodegradability test, the biodegradability of the PVA/modified-starch blends, therein PVA is blended with 1N AMS, shows better biodegradability. The result of bio-reaction kinetics experiment can evaluate the decomposition tendency of the PVA/starch blends up to any biodegradable rate under ambient environment. Using the kinetic model of the first order reaction, it is estimated that 16.20?years and 12.47?years will be needed for the PVA_BF-17/starch blends, containing 20 and 40% of CLS respectively, to be degraded up to 70% under ambient environment. In addition, it is 1.68?years for the PVA_BF-26 blends with the 40% 2N AMS under decomposition environment while it is 1.94?years for the 40% 1N AMS. Overall, the decomposition potential of PVA/AMS specimens is better than PVA/CLS specimens. Furthermore, the 1N(26P₆₀AS₄₀)₁₀₀G₂₀M₁ specimen is coincidence the biodegradable material criteria of Environmental Protection Administration (EPA) of Taiwan.     

Modification of an ecosystem model for filling medium-sized gaps in tower-based estimates of net ecosystem productivity

Gap filling of flux data is necessary to assist with periodic interruptions in the measurement data stream. The gap-filling model (GFM), first described in Xing et al. [Xing, Z., Bourque, C.P.-A., Meng, F.-R., Zha, T.-S., Cox, R.M., Swift, E., 2007. A simple net ecosystem productivity model for gap filling of tower-based fluxes: an extension of Landsberg's equation with modifications to the light interception term. Ecol. Model. 206, 250–262], was modified to account for the day-to-day control of net ecosystem productivity (NEP) by incorporating air and soil temperature as new controlling variables in the calculation of NEP. To account for the multiple-phase influences of air and soil temperature on plant growth we model ecosystem respiration as a function of soil and canopy respiration. The paper presents model development in an incremental fashion in order to quantify the contribution of individual model enhancements to the prediction of NEP during periods when air and soil temperature variations are important.     

Mercury and Organochlorine Contamination in Brown Trout (Salmo Trutta) and Arctic Charr (Salvelinus Alpinus) from High Mountain Lakes in Europe and the Svalbard Archipelago

High concentration of Hg, less volatile PCB congeners and p,p-DDE in Arctic charr from an arctic lake was mainly causedby biomagnification in the food chain where cannibalism was thedriving force. We suggest that low sediment fluxes of Hg, low net production of methyl mercury, and short food chains excludingpiscivory explain the low levels of Hg in the invertebrate feeding fish population in five European high mountain lakes.Concentrations of less volatile PCB congeners in insectivorous fish populations from the European high mountain lakes were mainly influenced by fish age and atmospheric deposition, indicated by the sediment inventory. Atmospheric deposition influenced by local sources may explain the higher concentrationsof pesticides (p,p-DDT, p,p-DDE and -HCH) observedin fish from the Pyrenees compared to the other sites. Theconcentrations of Hg and organochlorines did not exceedthe guidelines for fish consumption, except for Hg levelsin the oldest fish from the arctic lake.     

Aerosol chemical and optical properties during the Mt. Zirkel Visibility Study

Aerosol chemical and optical properties were measured near the Mt. Zirkel Wilderness Area in northwestern Colorado. Six-hour PM2.5 (particles with aerodynamic diameters less than 2.5 microm) mass concentrations and PM2.5 dry particle light scattering at 550 nm averaged 4.6 microg m(-3) and 8.6 Mm(-1), respectively. Sulfates, organic carbon, and geological material were the principle components of particle mass and light scattering. Hygroscopic growth was consistent with that expected for ammonium sulfate aerosols. Size distributions derived from three-wavelength (i.e., 450, 550, and 700 nm) nephelometer data were similar to those measured in other remote areas of the western USA. Quasi-dry chemical light scattering efficiencies derived using Mie theory were 3.6 m2 g(-1) for organic carbon, 2.5 m2 g(-1) for sulfates (ammonium sulfate and ammonium bisulfate), 2.6 m2 g(-1) for ammonium nitrate, and 1.76 m2 g(-1) for geological material. These values are lower than but consistent with previously reported results. Realistic efficiencies could not be derived using the multiple linear regression (MLR) approach.     

Dilution sampling and analysis of particulate matter in biomass-derived syngas

Thermochemical biomass gasification, followed by conversion of the produced syngas to fuels and electrical power, is a promising energy alternative. Real-world characterization of particulate matter (PM) and other contaminants in the syngas is important to minimize damage and ensure efficient operation of the engines it powers and the fuels created from it. A dilution sampling system is demonstrated to quantify PM in syngas generated from two gasification plants utilizing different biomass feedstocks: a BioMax?15 Biopower System that uses raw and torrefied woodchips as feedstocks, and an integrated biorefinery (IBR) that uses rice hulls and woodchips as feedstocks. PM_2.5 mass concentrations in syngas from the IBR downstream of the purification system were 12.8–13.7 μg·m⁻³, which were significantly lower than the maximum level for catalyst protection (500 μg·m⁻³) and were 2–3 orders of magnitude lower than those in BioMax?15 syngas (2247–4835 μg·m⁻³). Ultrafine particle number concentration and PM_2.5 chemical constituents were also much lower in the IBR syngas than in the BioMax?15. The dilution sampling system enabled reliable measurements over a wide range of concentrations: the use of high sensitivity instruments allowed measurement at very low concentrations (∼1 μg·m⁻³), while the flexibility of dilution minimized sampling problems that are commonly encountered due to high levels of tars in raw syngas (∼1 g·m⁻³).     

Health risk assessment of organochlorine pesticides with emphasis on DDTs and HCHs in abandoned agricultural soils

The aim of this study was to evaluate the consequence of changing land use from agriculture land to other use purposes with respect to OCPs non-cancer and cancer risk on human health, based on concentrations of DDTs and HCHs in soils collected from 55 locations representing 12 different land use types. There were no non-cancer risks of DDTs and γ-HCHs on adults and children, and there were very low cancer risks of DDD, o,p'-DDE, DDT, α-HCH, β-HCH, γ-HCH based on their total concentrations in all samples. Nonetheless, there were significant correlations of DDT to its metabolites (DDE and DDD) (r = 0.506 and r = 0.648) and DDE to DDD (r = 0.438) both at p < 0.01. OCP levels should be routinely monitored in different environmental media and food in order to verify whether there is fresh input. Their potential risks on human health should also be assessed.