Statistical approaches for identifying air pollutant mixtures associated with aircraft departures at los angeles international airport

Aircraft departures emit multiple pollutants common to other near-airport sources, making it challenging to determine relative source contributions. While there may not be unique tracers of aircraft emissions, examination of multipollutant concentration patterns in combination with flight activity can facilitate source attribution. In this study, we examine concentrations of continuously monitored air pollutants measured in 2008 near a departure runway at Los Angeles International Airport (LAX), considering single-pollutant associations with landing and takeoff (LTO) of the aircraft (LTO activity, weighted by LTO cycle fuel burn), as well as multipollutant predictors of binary LTO activity. In the single-pollutant analyses, one-minute average concentrations of carbon monoxide, carbon dioxide, nitrogen oxides, and sulfur dioxide are positively associated with fuel burn-weighted departures on the runway proximate to the monitor, whereas ozone is negatively associated with fuel burn-weighted departures. In analyses in which the flight departure is predicted by pollutant concentrations, carbon dioxide and nitrogen oxides are the best individual predictors, but including all five pollutants greatly increases the power of prediction compared to single-pollutant models. Our results demonstrate that air pollution impacts from aircraft departures can be isolated using time-resolved monitoring data, and that combinations of simultaneously measured pollutants can best identify contributions from flight activity.     

Wastewater treatment plant and landfills as sources of polyfluoroalkyl compounds to the atmosphere

Polyfluoroalkyl compounds (PFCs) were determined in air around a wastewater treatment plant (WWTP) and two landfill sites using sorbent-impregnated polyurethane foam (SIP) disk passive air samplers in summer 2009. The samples were analyzed for five PFC classes (i.e., fluorotelomer alcohols (FTOHs), perfluorooctane sulfonamides (FOSAs), sulfonamidoethanols (FOSEs), perfluoroalkyl sulfonic acids (PFSAs), and perfluoroalkyl carboxylic acids (PFCAs)) to investigate their concentration in air, composition and emissions to the atmosphere. ∑PFC concentrations in air were 3-15 times higher within the WWTP (2280-24?040 pg/m(3)) and 5-30 times higher at the landfill sites (2780-26?430 pg/m(3)) compared to the reference sites (597-1600 pg/m3). Variations in the PFC pattern were observed between the WWTP and landfill sites and even within the WWTP site. For example, FTOHs were the predominant PFC class in air for all WWTP and landfill sites, with 6:2 FTOH as the dominant compound at the WWTP (895-12?290 pg/m(3)) and 8:2 FTOH dominating at the landfill sites (1290-17?380 pg/m(3)). Furthermore, perfluorooctane sulfonic acid (PFOS) was dominant within the WWTP (43-171 pg/m(3)), followed by perfluorobutanoic acid (PFBA) (55-116 pg/m(3)), while PFBA was dominant at the landfill sites (101-102 pg/m(3)). It is also noteworthy that the PFCA concentrations decreased with increasing chain length and that the emissions for the even chain length PFCAs outweighed emissions for the odd chain length compounds. Furthermore, highly elevated PFC concentrations were found near the aeration tanks compared to the other tanks (i.e., primary and secondary clarifier) and likely associated with increased volatilization during aeration that may be further enhanced through aqueous aerosol-mediated transport. ∑PFC yearly emissions estimated using a simplified dispersion model were 2560 g/year for the WWTP, 99 g/year for landfill site 1, and 1000 g/year for landfill site 2. These results highlight the important role of WWTPs and landfills as emission sources of PFCs to the atmosphere.     

Potential sources of pesticides,PCBs, and PAHs to the atmosphere of the Great Lakes

A probabilistic model called the potential source contribution function (PSCF) has been used to estimate atmospheric source regions of polycyclic aromatic hydrocarbons (PAHs), chlorinated pesticides, and polychlorinated biphenyls (PCBs) to the Great Lakes. This model allows us to map each compound's source region on a 0.5 degrees x 0.5 degrees latitude/longitude grid centered over the Great Lakes basin. PCBs primarily have urban sources, the strengths of which vary. Like PCBs, PAHs show a strong urban signature, but these compounds also seem to come from rural sites. The source regions of PAH become less distinct as the molecular weight of the compound increases. Since reactivity increases with PAH size, this diminishing trend may be an indication that atmospheric degradation plays a large role in PAH transport. The pesticides have the strongest source regions and are typically transported the farthest, often from areas distant from the Great Lakes basin.     

Atmospheric methane: trends and cycles of sources and sinks

For more than 20 years the global emissions and the lifetime of methane have probably been constant, so the buildup of methane in the atmosphere has been slowing down for as long. During this time, there have been periodic events occurring every seven to eight years, when global methane concentrations increased by some 10 ppb and later fell back, in some cases due to temporary increases of emissions from the northern tropics that spread to the global scale. These conclusions are derived from the accumulated global observations that now span 23 years and define the role of human activities in the recent cycle of atmospheric methane.     

Uncertainty assessment of the breath methane concentration method to determine methane production of dairy cows

The breath methane concentration method uses the methane concentrations in the cow's breath during feed bin visits as a proxy for the methane production rate. The objective of this study was to assess the uncertainty of a breath methane concentration method in a feeder and its capability to measure and rank cows' methane production. A range of controlled methane fluxes from a so-called artificial reference cow were dosed in a feed bin, and its exhaled air was sampled by a tube inside the feeder and analyzed. The artificial reference cow simulates the lungs, respiratory tract, and rumen of a cow and releases a variable methane flux to generate a concentration pattern in the exhaled breath that closely resembles a real cow's pattern. The strength of the relation between the controlled methane release rates of the artificial reference cow and the measured methane concentrations was analyzed by linear regression, using the coefficient of determination (R²) and the residual standard error as performance indicators. The effect of error sources (source-sampling distance, air turbulence, and cow's head movement) on this relation was experimentally investigated, both under laboratory and barn conditions. From the laboratory to the dairy barn at the 30-cm sampling distance, the R²-value decreased from 0.97 to 0.37 and the residual standard error increased from 75 to 86 ppm as a result of barn air turbulence, the latter increasing to a theoretical 94 ppm if modeled variability due to cow's head movement was accounted for as well. In practice, the effect of these random errors can be compensated by sampling strategies including repeated measurements on each cow over time, thus increasing the distinctive power between cows. However, systematic errors that may disturb the relation between concentration and production rate, such as cow variation in air exhalation rate and air flow patterns around sampling locations that differ between barns, cannot be compensated by repeated measurements. As a result, the methane concentrations of breath air will vary between cows with the same methane production. We conclude that the capability of the breath concentration measurement method to adequately measure and rank methane production rates among cows is highly uncertain and requires further investigation into variation sources with a systematic nature.     

Review of methane mitigation technologies with application to rapid release of methane from the Arctic

Methane is the most important greenhouse gas after carbon dioxide, with particular influence on near-term climate change. It poses increasing risk in the future from both direct anthropogenic sources and potential rapid release from the Arctic. A range of mitigation (emissions control) technologies have been developed for anthropogenic sources that can be developed for further application, including to Arctic sources. Significant gaps in understanding remain of the mechanisms, magnitude, and likelihood of rapid methane release from the Arctic. Methane may be released by several pathways, including lakes, wetlands, and oceans, and may be either uniform over large areas or concentrated in patches. Across Arctic sources, bubbles originating in the sediment are the most important mechanism for methane to reach the atmosphere. Most known technologies operate on confined gas streams of 0.1% methane or more, and may be applicable to limited Arctic sources where methane is concentrated in pockets. However, some mitigation strategies developed for rice paddies and agricultural soils are promising for Arctic wetlands and thawing permafrost. Other mitigation strategies specific to the Arctic have been proposed but have yet to be studied. Overall, we identify four avenues of research and development that can serve the dual purposes of addressing current methane sources and potential Arctic sources: (1) methane release detection and quantification, (2) mitigation units for small and remote methane streams, (3) mitigation methods for dilute (<1000 ppm) methane streams, and (4) understanding methanotroph and methanogen ecology.     

如何选购复合气调保鲜包装机

复合气调保鲜包装机是在真空包装机、充氮包装机的基础上研发的一种全新的食品果蔬保鲜包装设备。其最大特点是解决了真空包装经高温灭菌后食品口感品味破坏较大，充氮包装要求无菌包装而投资较大的欠缺。通过复合气调包装，能确保食品原有口感，口味，保证了食品的原汁原味。     

TCE diffusion to the atmosphere in phytoremediation applications

The phytoremediation of trichloroethylene (TCE) and other chlorinated compounds has been studied over the past decade, and full-scale systems are in place. The results regarding TCE fates and removal pathways are inconclusive and conflicting, particularly the results regarding volatilization to the atmosphere. Research presented here demonstrates that TCE is taken up by trees and volatilized to the atmosphere. TCE diffusion along the transpiration pathway is shown to be the primary process for TCE volatilization, although volatilization can occur from both stems and leaves. Two concurrent processes influence the eventual fate: transport with transpiration stream through xylem tissues and diffusion from transpiration stream to atmosphere. TCE diffusion flux invariably decreased with height for trees planted in soil or grown hydroponically. In both laboratory experiments and field sampling, TCE concentrations in the transpiration stream (e.g., xylem tissues) decreased with elevation. In field samples, TCE concentrations also decreased in the radial direction, providing fundamental evidence for diffusion. The TCE concentrations in tissues responded linearly to the exposure concentrations at the roots, while TCE diffusion from tree stems was influenced by concentration and transpiration rates.     

造纸林基地建设的土地来源

提出贯彻国家关于造纸原料林建设的近期和中远期两个层次的意见,对土地来源问题提出建议.     

Modified atmosphere packaging to extend the shelf life of tomatoes

An experimental retail packaging system was used to compare the atmospheric com-position and relative humidity which developed within packs sealed with a range of plastic films with different permeability properties, and to study the effects of these conditions on the rate of ripening (as indicated by colour change) and sensory quality of tomatoes. In packs sealed with several polyvinylchloride (PVC) films or with K-resin (a butadiene-styrene copolymer), an atmosphere containing 3–9% CO₂+3−9% 0₂ developed within circa 3–4 days at 10 or 12.5°C. Ripening of part ripe fruit was retarded, but continued normally after the packs were perforated, with no obvious adverse effects on the smell, flavour or texture of the fruit. In packs sealed with less permeable films (e.g. cellulose acetate), the internal atmosphere equilibrated to 10–18% CO₂+ < 2% O₂, resulting in complete inhibition of ripening, a high incidence of rotting and tainting of the fruit. Very high (98% or above) relative humidity within sealed packs also encouraged fungal spoilage. The possible commercial applications and benefits of this type of modified atmosphere (MA) packaging are discussed.     

All-time releases of mercury to the atmosphere from human activities

Understanding the biogeochemical cycling of mercury is critical for explaining the presence of mercury in remote regions of the world, such as the Arctic and the Himalayas, as well as local concentrations. While we have good knowledge of present-day fluxes of mercury to the atmosphere, we have little knowledge of what emission levels were like in the past. Here we develop a trend of anthropogenic emissions of mercury to the atmosphere from 1850 to 2008-for which relatively complete data are available-and supplement that trend with an estimate of anthropogenic emissions prior to 1850. Global mercury emissions peaked in 1890 at 2600 Mg yr(-1), fell to 700-800 Mg yr(-1) in the interwar years, then rose steadily after 1950 to present-day levels of 2000 Mg yr(-1). Our estimate for total mercury emissions from human activities over all time is 350 Gg, of which 39% was emitted before 1850 and 61% after 1850. Using an eight-compartment global box-model of mercury biogeochemical cycling, we show that these emission trends successfully reproduce present-day atmospheric enrichment in mercury.     

Direct volatilization of naphthalene to the atmosphere at a phytoremediation site

Phytoremediation systems are known to reduce groundwater contamination by at least three major mechanisms: plant uptake, phytovolatilization, and enhanced rhizosphere bioremediation. The potential for such systems to enhance a fourth remediation pathway--direct surface volatilization of contaminants through the subsurface and into the atmosphere-has not yet been investigated in the field. A vertical flux chamber was used to measure direct surface volatilization of naphthalene over nine months at a creosote-contaminated site in Oneida, Tennessee, where a phytoremediation system of poplar trees was installed in 1997. A maximum flux of 23 microg m(-2) h(-1) was measured in August 2004, and naphthalene removal by the direct volatilization pathway is estimated to be 50 g yr(-1) at this site. Results suggest that direct volatilization fluxes are most strongly affected by the groundwater level (thickness of the saturated zone), soil moisture, and changes in atmospheric pressure. At this site, transpiration and canopy interception resulting from the phytoremediation system significantly reduce the saturated thickness, increasing the vertical concentration gradient of naphthalene in the groundwater and thus increasing the upward diffusive flux of naphthalene through the subsurface. The presence of the trees, therefore, promotes direct volatilization into the atmosphere. This research represents the first known measurement of naphthalene attenuation by the direct volatilization pathway.     

充分利用俄罗斯木材资源浅议

俄罗斯制浆造纸工业自1989年产量滑坡后,近年来开始复苏,产量上升,并将继续增长.它拥有世界上最丰富的木材资源,但尚未充分开发利用.在此基础上,笔者认为我国造纸企业将有机会与俄罗斯加强合作、合资,充分利用其木材资源生产我国紧缺的化学木浆.     

Modeling of TCE diffusion to the atmosphere and distribution in plant stems

Fate of chlorinated solvents in phytoremediation has been delineated by many discoveries made in recent years. Plant uptake, metabolism, rhizosphere degradation, accumulation, and volatilization were shown to occur to differing degrees for many organic contaminants including chlorinated solvents. Among these mechanistic findings, recent research confirmed that volatile organic compounds (VOCs) volatilize from stems and that the resulting diffusive flux to the atmosphere is related to exposure concentration and to height up the stem. A comprehensive model was developed based upon all identified fate and transport mechanisms for VOCs, including translocation in the xylem flow and diffusion. The dispersion and diffusion in the radial direction were considered as one process (effective diffusion) as the two could not be investigated individually. The mechanism-based model mathematically indicates an exponential decrease of concentrations with height. While an analytic solution for the comprehensive model was not attained, it can serve as a starting point for other modeling efforts. The comprehensive model was simplified in this work for practical application to experimentally obtained data on trichloroethylene (TCE) fate. Model output correlated well with experimental results, and effective diffusivities for TCE in plant tissues were obtained through the model calibrations. The simplified model approximated TCE concentrations in the transpiration stream as well as TCE volatilization to the atmosphere. Xylem transport, including advection, dispersion, and diffusion through cell walls with subsequent volatilization to the atmosphere, is a major fate for VOCs in phytoremediation.     

气调包装(MAP)在鲜肉保鲜中的应用

概述了气调包装现状,详细阐述了肉品气调包装保鲜的机理及其影响因素,最后对气调包装在鲜肉保鲜中的应用应注意的问题进行了探讨。     

Emission of nitrous oxide to the atmosphere from direct-drilled and ploughed clay soils

The emission of nitrous oxide to the atmosphere was measured for 2 years (1977-79) from two clay soils (Denchworth and Lawford series) that had either been directdrilled or ploughed. On almost all sampling occasions the emission from directdrilled plots exceeded that from the ploughed plots by factors ranging up to 15-fold. Rates of nitrous oxide loss reached peaks of 2.5-3.0 mg N m-² h-¹ (equivalent to 0.6-0.7 kg N ha-¹ day-¹) from the direct-drilled plots on the Denchworth soil. Emissions of nitrous oxide from the Lawford soil were only 10-20% of those from the Denchworth soil. The total amount of nitrous oxide-N lost during each year from the Denchworth soil was estimated to be 5.4-8.6 kg N ha-¹ from the direct-drilled plots and 0.9-5.6 kg N ha-¹ from the ploughed plots.     

Historical perspective of industrial lead emissions to the atmosphere from a Canadian smelter

Dated sediment cores from four remote Canadian Shield headwater lakes, where atmospheric deposition has been the only input of anthropogenic Pb, situated along a transect extending 300 km from a nonferrous metal smelter, were analyzed for both lead concentrations and isotopic composition; porewater samples collected at the same sites were analyzed for Pb and other geochemical variables. The depth distributions of stable Pb isotope ratios show the presence of several isotopically distinct Pb types since the preindustrial period. Lead from the smelter emissions had an isotopic signature (e.g., 206Pb/207Pb approximately 0.993) that was clearly distinct from those of Pb in aerosols collected at sites remotefrom point sources in Eastern Canada (e.g., 206Pb/207Pb usually approximately 1.15-1.20) and the United States (e.g., 206Pb/207Pb usually approximately 1.15-1.22), allowing the geographical area impacted by the smelter Pb emissions to be traced. On the basis of the sediment Pb isotopic composition, it is estimated that lead from the smelter accounts for 89%, 88%, and 5-34% of the total inventory of anthropogenic Pb deposited in the sediments of lakes located 10, 25, and 150 km from the smelter, respectively; but lead from this point source was not detected in sediments of a fourth lake that is 300 km from the smelter. We also estimate that the amount of smelter-derived Pb deposited within a distance of 150 km is equivalent to 5-10% of the amount released by leaded gasoline combustion in all of Canada. Sharp decreases in the recent Pb fluxes to lake sediments indicate that the measures taken to mitigate metal emissions from the smelter were effective.