Soot in the arctic snowpack: a cause for perturbations in radiative transfer

Recent data collected in the Arctic have demonstrated the transport of atmospheric aerosol of anthropogenic origin into that region. Concern over the radiative effect of the highly-absorbing soot component of this aerosol has resulted in a variety of atmospheric sampling efforts aimed at assessing the climatic impact of this component. However, little attention has been given to the measurement of soot deposited on the Arctic snowpack and the resulting perturbation of snow albedo, snowmelt rates and radiative transfer. Here we report measurements of light-absorbing material in the Arctic snowpack for longitudes from 25 E to 160 W. The contributions to light absorption due to natural crustal and soot aerosol are identified by their wavelength dependence. Reductions in Arctic snow albedo of one to several percent appear probable for the soot/ice mass fractions obtained to date. Estimates of the impact of this reduced albedo on the Arctic radiation budget over a season are shown to approximately equal that of the Arctic haze itself. The absorption of shortwave radiation by the springtime snowpack is estimated to be 5–10% higher than that of soot-free snow for this data.     

VOC concentrations measured in personal samples and residential indoor,outdoor and workplace microenvironments in EXPOLIS-Helsinki,Finland

Thirty target volatile organic compounds (VOC) were analyzed in personal 48-h exposure samples and residential indoor, residential outdoor and workplace indoor microenvironment samples as a component of EXPOLIS-Helsinki, Finland. Geometric mean residential indoor concentrations were higher than geometric mean residential outdoor concentrations for all target compounds except hexane, which was detected in 40% of residential outdoor samples and 11% of residential indoor samples, respectively. Geometric mean residential indoor concentrations were significantly higher than personal exposure concentrations, which in turn were significantly higher than workplace concentrations for compounds that had strong residential indoor sources (d-limonene, alpha pinene, 3-carene, hexanal, 2-methyl-1-propanol and 1-butanol). 40% of participants in EXPOLIS-Helsinki reported personal exposure to environmental tobacco smoke (ETS). Participants in Helsinki that were exposed to ETS at any time during the 48-h sampling period had significantly higher personal exposures to benzene, toluene, styrene, m,p-xylene, o-xylene, ethylbenzene and trimethylbenzene. Geometric mean ETS-free workplace concentrations were higher than ETS-free personal exposure concentrations for styrene, hexane and cyclohexane. Geometric mean personal exposures of participants not exposed to ETS were approximately equivalent to time weighted ETS-free indoor and workplace concentrations, except for octanal and compounds associated with traffic, which showed higher geometric mean personal exposure concentrations than any microenvironment (o-xylene, ethylbenzene,benzene, undecane, nonane, decane, m,p-xylene, and trimethylbenzene). Considerable differences in personal exposure concentrations and residential levels of compounds with mainly indoor sources suggested differences in product types or the frequency of product use between Helsinki, Germany and the United States.     

Computing surface concentration fluxes of trace gases from a variational method using measured variance and single-level concentration data

Surface fluxes of O₃, CO₂ and SO₂ were estimated from a variational method by using measured concentrations and variances of these trace gases. The measurements were taken over a deciduous forest when it was fully leafed during the summer of 1988 and when it was leafless during the winter of 1990. A flux–variance relation and a flux–gradient relation were employed as constraints in a cost function which is minimized to find the optimal estimate of concentration fluxes of the gases under study. Fluxes of O₃, CO₂ and SO₂ from the variational method were compared with fluxes estimated by the flux–variance relation and measured using an eddy correlation technique. Results show that the variational method improves the estimates of fluxes.     

东莞地区PM2.5湿清除的观测研究

通过对东莞市2013—2017年降水、PM_2.5观测数据统计研究发现,降雨及PM_2.5浓度存在负相关关系,降雨对PM_2.5具有一定的清除效果.PM_2.5浓度下降的降水过程有376次,浓度上升的降水过程有333次,部分降水过程浓度出现明显反弹,应与气溶胶再悬浮机制有关.在所有PM_2.5初始浓度低于40 μg·m^-3的个例中,浓度下降的个例占比约49.4%,而当PM_2.5初始浓度高于40 μg·m^-3时,浓度下降的个例占比约71.2%,说明PM_2.5粒子数量较多时,雨滴对粒子的捕获能力较强,降雨前PM_2.5的初始浓度可以作为判断降雨后PM_2.5浓度是否下降的预报依据.雨强小,也是造成雨后PM_2.5浓度反弹的原因.对于有效清除个例,雨强与清除率存在正相关关系,雨强越强,整体的清除作用有所加强.降水持续时间是影响PM_2.5清除作用的重要因素,持续时间超过6 h的小雨降水过程能达到40%的清除率效果,中雨以上降水过程持续时间越长,PM_2.5的清除效果越好.在浓度反弹的个例中,在低的初始浓度条件下,降水强度与降水持续时间对PM_2.5浓度反弹影响均较小,在初始浓度大于30 μg·m^-3的条件下,平均反弹幅度收窄,初始浓度的增加,使得雨滴与颗粒物之间的碰并作用加强,降水强度的增大,使这种碰并作用进一步加强,进而制约了PM_2.5浓度反弹的幅度.降雨末期,细粒径颗粒物数浓度回升明显,小雨滴蒸发使细粒子脱离再次在空中悬浮,是造成雨后颗粒物浓度出现回升的主要原因.     

Seasonal and diel variation of atmospheric mercury concentrations in the Reno (Nevada,USA) airshed

This paper describes total gaseous mercury (TGM) concentrations measured in Reno, Nevada from 2002 to 2005. The 3-year mean and median air Hg concentrations were 2.3 and 2.1 ng m⁻³, respectively. Mercury concentrations exhibited seasonality, with the highest concentrations in winter, and the lowest in summer and fall. A well-defined diel pattern in TGM concentration was observed, with maximum daily concentrations observed in the morning and minimum in the afternoon. A gradual increase of TGM concentration was observed in the evening and over night. The early morning increase in TGM was likely due to activation of local surface emission sources by rising solar irradiance and air temperature. The subsequent decline and afternoon minimum in TGM were likely related to increased vertical mixing and the buildup of atmospheric oxidants during the day resulting in increased conversion to oxidized species that are quickly deposited, coupled with weakening of the surface emissions processes. The described diel pattern was seasonally modulated with the greatest amplitude in variation of TGM concentrations occurring in the summer. It is suggested based on the comparison of diel TGM pattern with other gaseous pollutants that natural source surface emissions are a dominant source of TGM in the study area.     

Long-term Environmental Impact of Oil Spills

Oil contamination may persist in the marine environment for many years after an oil spill and, in exceptional cases such as salt marshes and mangrove swamps, the effects may be measurable for decades after the event. However, in most cases, environmental recovery is relatively swift and is complete within 2–10 years. Where oil has been eliminated from the scene, the long-term environmental impacts are generally confined to community structure anomalies that persist because of the longevity of the component species.     

Distribution of seasonal SO2 emissions from fuel combustion and industrial activities in Shanxi province,China, with 1/6°×1/4° longitude/latitude resolution

Spatial distribution of SO₂ emission inventory for 1994 from fuel combustion and industrial activities in Shanxi province, the Peoples’ Republic of China, has been created with 1/6°×1/4° latitude/longitude resolution. Total annual SO₂ emissions in 1994 in the province were estimated to be 669 GgS, of which 180 GgS were emitted in winter, 170 GgS in spring, 156 GgS in summer, and 163 GgS in fall. For the first time this emission inventory includes SO₂ emissions from village and township enterprises. Although SO₂ emissions from major industries were under control, SO₂ emissions from village and township enterprises became the major threat to the environment in the province.     

The aerosol at Barrow,Alaska: long-term trends and source locations

Aerosol data consisting of condensation nuclei (CN) counts, black carbon (BC) mass, aerosol light scattering (SC), and aerosol optical depth (AOD) measured at Barrow, Alaska from 1977 to 1994 have been analyzed by three-way positive matrix factorization (PMF3) by pooling all of the different data into one large three-way array. The PMF3 analysis identified four factors that indicate four different combinations of aerosol sources active throughout the year in Alaska. Two of the factors (F1, F2) represent Arctic haze. The first Arctic haze have factor F1 is dominant in January–February while the second factor F2 is dominant in March–April. They appear to be material that is generally ascribed to long-range transported anthropogenic particles. A lower ratio of condensation nuclei to scattering coefficient loadings is obtained for F2 indicating larger particles. Factor F3 is related to condensation nuclei. It has an annual cycle with two maxima, March and July–August indicating some involvement of marine biogenic sources. The fourth factor F4 represents the contribution to the stratospheric aerosol from the eruptions of El Chichon and Mt. Pinatubo. No significant long-term trend for F1 was detected while F2 shows a negative trend over the period from 1982 to 1994 but not over the whole measurement period. A positive trend of F3 over the whole period has been observed. This trend may be related to increased biogenic sulfur production caused by reductions in the sea-ice cover in the Arctic and/or an air temperature increase in the vicinity of Barrow. Potential source contribution function (PSCF) analysis showed that in winter and spring during 1989 to 1993 regions in Eurasia and North America are the sources of particles measured at barrow. In contrast to this, large areas in the North Pacific Ocean and the Arctic Ocean was contributed to observed high concentrations of CN in the summer season. Three-way positive matrix factorization was an effective method to extract time-series information contained in the measured quantities. PSCF was useful for the identification possible source areas and the potential pathways for the Barrow aerosol. The effects of long-distance transport, photochemical aerosol production, emissions from biogenic activities in the ocean, volcanic eruptions on the aerosol measurements made at Barrow were extracted using this combined methodology.     

Aerosol black carbon and ozone measurements at Mt. Krvavec EMEP/GAW station,Slovenia

We report on one-year continuous measurements of aerosol black carbon at the EMEP/GAW regional air quality station on Mt. Krvavec in Slovenia, where ozone concentration has been monitored routinely since 1991. The results show several characteristic BC and O₃ concentration patterns with positive and negative correlation.     

A generalized analytical solution for turbulent dispersion with inhomogeneous wind and diffusion coefficient

A technique is presented to solve analytically the turbulent diffusion equation for the concentration of a passive contaminant emitted from an elevated continuous source into the atmosphere. A generalized method of solution using Sturm–Liouville and WKB theories is developed to overcome difficulties due to the height‐dependent wind velocity and diffusion coefficient appearing in the diffusion equation. The method presented in this paper is able to derive an asymptotic expression for the concentration obtained from the solution of the atmospheric diffusion equation which involves explicitly inhomogeneous wind velocity and diffusion coefficient. The diffusion equation model derived from this method can be applied in a practical prediction of contaminant concentration in a turbulent atmosphere. This revised version was published online in August 2006 with corrections to the Cover Date.