基于卫星遥感数据(AOD)估算PM2.5的研究进展

雾霾天气的频繁出现,不断向人们警示中国大气环境污染的严重性.细颗粒物PM2.5作为空气质量评价指标之一,由于粒径小、为有毒性物质提供载体的特性,对人们的健康和生活产生很大的负面影响.近年来,PM2.5的相关研究引起了世界各国研究者的广泛关注,通过地基手段获得PM2.5质量浓度受到环境、地理等因素的限制,而利用卫星遥感技术估算地面PM2.5质量浓度,覆盖面广、估算精度可靠,对环境污染监测和治理具有重要意义.在综合了国内外关于气溶胶光学厚度(AOD)估算PM2.5文献的基础上,对AOD和PM2.5的数据源和估算的方法及手段作了简要介绍,分析总结了AOD与PM2.5相关性与PM2.5遥感估算的模型,并展望了未来PM2.5研究的发展方向.     

Elemental and individual particle analysis of atmospheric aerosols from high Himalayas

Atmospheric aerosols were collected during the scientific expedition to Mt. Qomolangma (Everest) in May–June, 2005. The elemental concentrations of the aerosols were determined by inductively coupled plasma mass spectrometry. This yielded data for the concentration of 14 elements: Na, Mg, Al, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, and Pb. The mean elemental concentrations were generally comparable with those from central Asia and the Arctic, while much higher than those from Antarctic. Size, morphology, and chemical composition of 900 individual aerosol particles were determined by scanning electron microscopy and energy-dispersive X-ray microanalysis. Based on morphology and elemental composition, the particles were clustered into eight groups: soot (8%), tar ball (3%), alumosilicates/silica (55%), calcium sulfate (16%), Ca/Mg carbonate (2%), Fe/Ti-rich particles (3%), Pb-rich particles (1%), and biological particles (12%). The sampling site, located at 6,520 m in the Himalayas, is particularly remote and located at high altitude. Nonetheless, high aerosol enrichment factors for copper, chromium, lead, nickel, vanadium, and zinc all suggest the influence of long-range transported pollution, while enrichment in calcium and the presence of alumino-silicates in individual particle analyses indicates a distinct mineral dust influence. The backward air mass trajectories showed that the northwestern part of India may contribute to the atmospheric aerosol in the central high Himalayas.     

Effects of biochar addition on greenhouse gas emissions and microbial responses in a short-term laboratory experiment

Biochar application to soil has drawn much attention as a strategy to sequester atmospheric carbon in soil ecosystems. The applicability of this strategy as a climate change mitigation option is limited by our understanding of the mechanisms responsible for the observed changes in greenhouse gas emissions from soils, microbial responses, and soil fertility changes. We conducted an 8-wk laboratory incubation using soils from PASTURE (silt loam) and RICE PADDY (silt loam) sites with and without two types of biochar (biochar from swine manure [CHAR-M] and from barley stover [CHAR-B]). Responses to addition of the different biochars varied with the soil source. Addition of CHAR-B did not change CO and CH evolution from the PASTURE or the RICE PADDY soils, but there was a decrease in NO emissions from the PASTURE soil. The effects of CHAR-M addition on greenhouse gas emissions were different for the soils. The most substantial change was an increase in NO emissions from the RICE PADDY soil. This result was attributed to a combination of abundant denitrifiers in this soil and increased net nitrogen mineralization. Soil phosphatase and N-acetylglucosaminidase activity in the CHAR-B-treated soils was enhanced compared with the controls for both soils. Fungal biomass was higher in the CHAR-B-treated RICE PADDY soil. From our results, we suggest CHAR-B to be an appropriate amendment for the PASTURE and RICE PADDY soils because it provides increased nitrogen availability and microbial activity with no net increase in greenhouse gas emissions. Application of CHAR-M to RICE PADDY soils could result in excess nitrogen availability, which may increase NO emissions and possible NO leaching problems. Thus, this study confirms that the ability of environmentally sound biochar additions to sequester carbon in soils depends on the characteristics of the receiving soil as well as the nature of the biochar.     

Can conservation of single surrogate species protect co-occurring species?

Conservation of surrogate species is expected to benefit co-occurring species with similar distributions that share the same habitat, yet the usefulness of this approach to protect nontarget species has been extensively challenged. In this study, we aimed to assess whether co-occurring species could be afforded protection under the conservation of two proposed surrogate species, the giant panda and the takin. We undertook a thorough study on the habitat requirements of these two endangered species, based on the analysis of their habitat preferences. The results revealed that the giant panda exhibits more specialized habitat preferences than does the takin and that habitat separation between these species mainly reflected differences in their dietary requirements and preferences. We suggest that these differences might facilitate their coexistence in sympatric areas. Meanwhile, results of a discriminant function analysis showed that protection of giant pandas would protect 82.1 % of the panda’s habitat, but only 25.4 % of the takin’s habitat and just 57.0 % of the joint habitats of these species. Importantly, our results also showed that a joint surrogate species approach to conservation would protect 86.9 % of the panda’s habitat, 53.7 % of the takin’s habitat, and 72.2 % of the joint habitats of these species. This is a higher degree of habitat protection than the single surrogate conservation of pandas. We conclude that the joint surrogate species approach should be adopted to improve biodiversity conservation.     

Physicochemical properties of chars at different treatment temperatures

In this study, the physicochemical properties of the char of Indonesian SM coal following heat treatment at various temperatures were evaluated using X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and morphological and specific surface area analysis. Based on these analyses, heat treatment of coal was determined to be the most effective in increasing the coal rank. In the XPS analysis, the C–O and C–O–C groups and quaternary-N species were found to be of a lower grade coal when the pretreatment temperature decreased, meanwhile the C–C group and pyridinic species increased. In the FT-IR analysis, the collapse of the C–O and C–O–C group was observed due to the collapse of the ether group. In SEM and Brunauer–Emmett–Teller (BET) analysis, a decrease in the ether group was shown to be accompanied with the formation of micropores.

Implications Recently, XPS analyses have been reported as coal surface analysis. Usually, they have reported the analysis of the coals with different rank. This study investigated the coal surface characteristics of the coals pretreated at different temperature using various analyses (BET, SEM, XPS, FT-IR), and this study can be the basis for other research and applications.     

1986 APCA Government Agencies Directory

Carbonaceous species (organic carbon [OC] and elemental carbon [EC]) and inorganic ions of particulate matter less than 2.5 μm (PM_2.5) were measured to investigate the chemical characteristics of long-range-transported (LTP) PM_2.5 at Gosan, Jeju Island, in Korea in the spring and fall of 2008–2012 (excluding 2010). On average, the non-sea-salt (nss) sulfate (4.2 µg/m³) was the most dominant species in the spring, followed by OC (2.6 µg/m³), nitrate (2.1 µg/m³), ammonium (1.7 µg/m³), and EC (0.6 µg/m³). In the fall, the nss-sulfate (4.7 µg/m³) was also the most dominant species, followed by OC (4.0 µg/m³), ammonium (1.7 µg/m³), nitrate (1.1 µg/m³), and EC (0.7 µg/m³). Both sulfate and OC were higher in the fall than in the spring, possibly due to more common northwest air masses (i.e., coming from China and Korea polluted areas) and more frequent biomass burnings in the fall. There was no clear difference in the EC between the spring and fall. The correlation between OC and EC was not strong; thus, the OC measured at Gosan was likely transported across a long distance and was not necessarily produced in a manner similar to the EC. Distinct types of LTP events (i.e., sulfate-dominant LTP versus OC-dominant LTP) were observed. In the sulfate-dominant LTP events, air masses directly arrived at Gosan without passing over the Korean Peninsula from the industrial area of China within 48 hr. During these events, the aerosol optical depth (AOD) increased to 1.63. Ionic balance data suggest that the long-range transported aerosols are acidic. In the OC-dominant LTP event, a higher residence time of air masses in Korea was observed (the air masses departing from the mainland of China arrived at the sampling site after passing Korea within 60–80 hr).

Implications:?In Northeast Asia, various natural and anthropogenic sources contribute to the complex chemical components and affect local/regional air quality and climate change. Chemical characteristics of long-range-transported (LTP) PM_2.5 were investigated during spring and fall of 2008, 2009, 2011, and 2012. Based on air mass types, sulfate-dominant LTP and OC-dominant LTP were observed. A long-term variation and chemical characteristics of PM_2.5 along with air mass and satellite data are required to better understand long-range-transported aerosols.     

人工泳池水质的模糊综合评判及分析

用模糊数学方法 ,处理人工泳池水质监测数据 ,综合评判泳池水质状况 ,分析水质参数间关系 ,探讨了该方法应用的可能性     

Removal of tetracycline from water by Fe-Mn binary oxide

Significant concerns have been raised over the presence of antibiotics including tetracyclines in aquatic environments. A series of Fe-Mn binary oxide with different Fe:Mn molar ratios was synthesized by a simultaneous oxidation and coprecipitation process for TC removal. Results showed that Fe-Mn binary oxide had higher removal efficiency than that of hydrous iron oxide and hydrous manganese oxide, and that the oxide with a Fe:Mn molar ratio of 5:1 was the best in removal than other molar ratios. The tetracycline removal was highly pH dependent. The removal of tetracycline decreased with the increase of initial concentration, but the absolute removal quantity was more at high concentration. The presence of cations and anions such as Ca²⁺, Mg²⁺, CO₃^2- and SO₄^2- had no significant effect on the tetracycline removal in our experimental conditions, while SiO₃^2- and PO₄^3- had hindered the adsorption of tetracycline. The mechanism investigation found that tetracycline removal was mainly achieved by the replacement of surface hydroxyl groups by the tetracycline species and formation of surface complexes at the water/oxide interface. This primary study suggests that Fe-Mn binary oxide with a proper Fe:Mn molar ratio will be a very promising material for the removal of tetracycline from aqueous solutions.     

Gas phase trichloroethylene removal at low concentration using activated carbon fiber

The breakthrough adsorption behaviors of gas phase trichloroethylene in a packed bed of activated carbon fibers(ACF) were investigated. The specific surface area of the ACF was 600 m^2/g, 1400 m^2/g and 1600 m^2/g, respectively, and the concentration of trichloroethylene ranged from 270 mg/m^3 to 2700 mg/m^3 . Results showed that the capacity of adsorption increased with increasing specific surface area, the relationship between the logarithms of 10% breakthrough time and concentration was approximately linear over the experimental range, the breakthrough time decreased with increasing temperature and humidity. The breakthrough curves at different inlet concentration or different temperature can be predicted by several simple theoretical models with good agreements.     

有机酸强化Fe(Ⅲ)还原介导的Shewanella oneidensis MR-1降解磺胺甲噁唑

在实验室条件下,研究了Shewanella oneidensis MR-1对磺胺甲噁唑（Sulfamethoxazole,SMX）的降解特性以及低分子有机酸强化Fe（Ⅲ）还原介导的S.oneidensis MR-1对SMX的降解.结果表明,S.oneidensis MR-1对不同浓度SMX的降解能力与体系中的有机酸和Fe（Ⅲ）密切相关.低浓度SMX对其生长影响不大,高浓度时细菌生长则受到抑制,进而抑制SMX的降解率.当低分子有机酸单独加入体系后,S.oneidensis MR-1对SMX的最大降解率为58.5%;Fe（Ⅲ）单独加入体系后,S.oneidensis MR-1对SMX的最大降解率为67.6%.此外,当柠檬酸和Fe（OH）₃同时加入体系后,S.oneidensis MR-1对SMX生物降解和铁还原作用促进效果最显著,培养5 d后SMX降解率为90.3%.最后,采用液相色谱-质谱联用仪（LC-MS）对SMX的降解中间产物进行了分析,推测SMX的可能降解途径是由S-N键断裂引起的.本研究以期为地下水污染场地修复提供理论依据.