吸湿性播撒对暖性对流云减雨影响的数值模拟

利用以色列特拉维夫大学二维面对称分档云模式（two-dimensional slab-symmetric detailed spectral bin microphysical model of Tel Aviv University）,对2016年9月4日16:00（北京时）前后我国华东地区的一次暖性浅对流云降水过程进行模拟,模式模拟的强回波中心高度和最大回波强度范围与观测基本一致。并在此基础上进行了小于1 μm的吸湿性核的播撒减雨试验,分别考虑了不同播撒时间、不同播撒高度以及不同播撒剂量的敏感性测试。结果表明:在云的发展阶段早期播撒能起到更好的减雨效果,播撒时间越早对大粒子生长过程的抑制作用越强,随着播撒时间向后推移,受抑制作用最显著的粒径段向小粒径端偏移;在云中心过饱和度大的区域下方进行播撒,减雨效果更加明显,当播撒剂量为350 cm-3时,地面累积降水量减少率可达23.3%;另外,随着播撒剂量的增加,减雨效果更加显著,甚至能达到消雨的效果。因此,在暖性浅对流云中合理地播撒小于1 μm的吸湿性核能达到较好的减雨或消雨效果。     

A Closure Study of Aerosol Hygroscopic Growth Factor during the 2006 Pearl River Delta Campaign

Measurements of aerosol physical, chemical and optical parameters were carried out in Guangzhou, China from 1 July to 31 July 2006 during the Pearl River Delta Campaign. The dry aerosol scattering coefficient was measured using an integrating nephelometer and the aerosol scattering coefficient for wet conditions was determined by subtracting the sum of the aerosol absorption coefficient, gas scattering coefficient and gas absorption coefficient from the atmospheric extinction coefficient. Following this, the aerosol hygroscopic growth factor, f(RH), was calculated as the ratio of wet and dry aerosol scattering coefficients. Measurements of size-resolved chemical composition, relative humidity (RH), and published functional relationships between particle chemical composition and water uptake were likewise used to find the aerosol scattering coefficients in wet and dry conditions using Mie theory for internally- or externally-mixed particle species [(NH₄)₂SO₄, NH₄NO₃, NaCl, POM, EC and residue]. Closure was obtained by comparing the measured f(RH) values from the nephelometer and other in situ optical instruments with those computed from chemical composition and thermodynamics. Results show that the model can represent the observed f(RH) and is appropriate for use as a component in other higher-order models.     

Changes in dissolved organic matter (DOM) amount and composition along nested headwater stream locations during baseflow and stormflow

Amount and composition of dissolved organic matter (DOM) were evaluated for multiple, nested stream locations in a forested watershed to investigate the role of hydrologic flow paths, wetlands and drainage scale. Sampling was performed over a 4‐year period (2008–2011) for five locations with drainage areas of 0.62, 3.5, 4.5, 12 and 79 ha. Hydrologic flow paths were characterized using an end‐member mixing model. DOM composition was determined using a suite of spectrofluorometric indices and a site‐specific parallel factor analysis model. Dissolved organic carbon (DOC), humic‐like DOM and fluorescence index were most sensitive to changes with drainage scale, whereas dissolved organic nitrogen, specific UV absorbance, Sr and protein‐like DOM were least sensitive. DOM concentrations and humic‐like DOM constituents were highest during both baseflow and stormflow for a 3.5‐ha catchment with a wetland near the catchment outlet. Whereas storm‐event concentrations of DOC and humic DOM constituents declined, the mass exports of DOC increased with increasing catchment scale. A pronounced dilution in storm‐event DOC concentration was observed at peak stream discharge for the 12‐ha drainage location, which was not as apparent at the 79‐ha scale, suggesting key differences in supply and transport of DOM. Our observations indicate that hydrologic flow paths, especially during storms, and the location and extent of wetlands in the catchment are key determinants of DOM concentration and composition. This study furthers our understanding of changes in DOM with drainage scale and the controls on DOM in headwater, forested catchments. Copyright © 2014 John Wiley & Sons, Ltd.     

Satellite-measured atmospheric aerosol content in Korea: anthropogenic signals from decadal records

Spatiotemporal characteristics and anthropogenic signals of aerosol optical thickness (AOT) distributions over Korea are investigated in this study using AOT time-series data from the Moderate Resolution Imaging Spectroradiometer (MODIS). AOT observations, a quantitative measure of the atmospheric quality, had significant geographical variations during the study period (2000–2010). Comparing metro cities or counties with similar populations, western regions showed higher AOT values than eastern regions. Particular matter with a diameter < 10 µm (PM₁₀), including aeolian dust or yellow dust, is the primary component of atmospheric aerosols, and their transport into the region has shown a strong seasonal pattern with its peak from March to April and lows from July to September. These seasonal dust patterns, however, did not correspond well to temporal AOT records, which typically reached the maximum level in June nationwide. Rather, widespread regional fire events and humidity showed significant correlations with AOT time-series. This correlation rapidly increased as the range of fire occurrence was extended to the west as far as 115°E. The relative humidity also had a significant correlation with AOT during the month of June. In addition to urban emission of anthropogenic aerosols, regional biomass burning and secondary growth of hygroscopic aerosols are considered important contributors to the degradation of the atmospheric environment during the non-Asian Dust season over the Korean Peninsula.     

Water-soluble organics in atmospheric particles: A critical review of the literature and application of thermodynamics to identify candidate compounds

Although organic compounds typically constitute a substantial fraction of the fine particulate matter (PM) in the atmosphere, their molecular composition remains poorly characterized. This is largely because atmospheric particles contain a myriad of diverse organic compounds, not all of which extract in a single solvent or elute through a gas chromatograph; therefore, a substantial portion typically remains unanalyzed. Most often the chemical analysis is performed on a fraction that extracts in organic solvents such as benzene, ether or hexane; consequently, information on the molecular composition of the water-soluble fraction is particularly sparse and incomplete.This paper investigates theoretically the characteristics of the water-soluble fraction by splicing together various strands of information from the literature. We identify specific compounds that are likely to contribute to the water-soluble fraction by juxtaposing observations regarding the extraction characteristics and the molecular composition of atmospheric particulate organics with compound-specific solubility and condensibility for a wide variety of organics. The results show that water-soluble organics, which constitute a substantial fraction of the total organic mass, include C2 to C7 multifunctional compounds (e.g., diacids, polyols, amino acids). The importance of diacids is already recognized; our results provide an impetus for new experiments to establish the atmospheric concentrations and sources of polyols, amino acids and other oxygenated multifunctional compounds.     

GBPP－100型地面雨滴谱仪测量的可靠性

用ＧＢＰＰ－１００型地面雨滴谱仪与吸水纸斑，点法进行同步观测，对比分析ＧＢＰＰ－１００型地面雨滴谱仪测量的可靠性。结果表明：（１）两种方法测量雨滴谱所得资料除平均直径、均立方根直径相似性稍差外，其它特征量的线性相关显著性水平均为０．００５；（２）两种方法所得雨滴谱资料除平均直径、均立方根直径、降水强度稍有差异外，其它特征量均无显著差异。     

Estimation of PM_(2.5) Mass Concentration from Visibility

Aerosols in the atmosphere not only degrade visibility, but are also detrimental to human health and transportation. In order to develop a method to estimate PM_2.5 mass concentration from the widely measured visibility, a field campaign was conducted in Southwest China in January 2019. Visibility, ambient relative humidity(RH), PM_2.5 mass concentrations and scattering coefficients of dry particles were measured. During the campaign, two pollution episodes, i.e., from 4-9 Ja...     

固相萃取—高温裂解—气相色谱质谱法测定西台晶间卤水中溶解性有机质

采用3种固相萃取材料(C18、XAD-8/4和PPL)分离富集西台吉乃尔盐湖卤水中的溶解性有机物(DOM),通过总有机碳/总氮分析(TOC/TN)、紫外—可见光谱分析、元素分析、傅里叶变换红外光谱分析(FTIR)、高温裂解—气相色谱质谱联用仪(Py-GC/MS)等对富集的有机物进行表征和分析方法比较。结果表明,西台吉乃尔盐湖卤水中的溶解性有机物主要有多糖类,芳香类、含氮类有机物,烷烃烯烃类化合物。PPL,C18和XAD-8/4的回收率分别为40±2%,7±2%和16±1%,虽然C18和XAD-8/4回收率较低,但3种吸附剂都有各自的特点,C18较易吸附烷烃烯烃类有机物,XAD-8/4较易吸附芳香类有机物,PPL较易吸附含N类有机物和多糖类有机物。     

Spatio-temporal changes in totally and enzymatically hydrolyzable amino acids of superficial sediments from three contrasted areas

Spatio-temporal changes in totally and enzymatically hydrolyzable amino acids (THAA and EHHA) and EHAA/THAA ratios of superficial sediments were assessed during 1997-1999 in three areas (i.e., the Gulf of Lions, the Bay of Biscay, and Central Chile) differing in their primary productivity. In all three areas, and even off Central Chile where a strong El Niño event took place during 1997-1998, spatial changes were always much greater than temporal ones. The factors affecting the spatial distributions of amino acid concentrations differed among areas. In the Gulf of Lions, sediment granulometry was apparently the most important driving force of THAA, EHAA, and EHAA/THAA, and there was no marked difference between stations located on the open slope and those in submarine canyons. Conversely, in the Bay of Biscay, there were clear differences between the stations located off Cap-Breton, on the open slope, and those in the Cap-Ferret canyon; the latter two featuring lower EHAA and THAA but higher EHAA/THAA. This pattern is likely to result from the predominance of different sources of organic matter and especially from the importance of continental inputs to the Cap-Breton canyon. Off Central Chile, amino acid concentrations and ratios were both maximal around 100 m depth, probably reflecting the interaction between the primary productivity gradient and the presence of an oxygen minimum zone (OMZ) reducing the degradation of sedimentary organics. When comparing the average values collected in the three areas studied, THAA and EHAA were highest in Central Chile, intermediate in the Bay of Biscay and lowest in the Gulf of Lions. EHAA/THAA ratios were also highest in Central Chile but were lowest in the Bay of Biscay. Differences between the Gulf of Lions and the Bay of Biscay could have been affected by sampling design. In Central Chile, the use of labile organic carbon to total organic carbon (C-LOM/TOC) and EHAA/THAA as indices of organic matter lability led to very similar results. This was not the case in the Bay of Biscay. It is therefore argued that the use of C-LOM/TOC should be restricted to highly productive areas.     

A comparison of two techniques for the isolation of adsorbed dissolved organic material from seawater

¹³C solid-phase NMR and pyrolysis-chemical ionization mass spectrometry were used to characterize adsorbed organic material isolated on an XAD-2 macroreticular resin. Pyrolysis-chemical ionization mass spectrometry was used directly to fingerprint the organics sorbed to a titanium foil exposed in the same marine environment. The XAD-2 isolate was shown to be fractionated relative to the native material and contaminated with the isolation resin.