干旱区中小城市降雪中金属元素沉降通量研究

文章以干旱区中小城市昌吉市为研究区，选择2011年12月至2012年2月期间较为典型的6场次降雪进行采样，利用ICP-MS测定降雪中20种金属元素，并探讨金属元素的沉降通量、富集特征及其来源。研究表明，降雪中Al的年沉降通量最大，为10.32 mg/m²；Fe、Ba、Zn、V、Cu的年沉降通量次之，集中在1.40~6.11 mg/m²；As、Ni、Mn、Cr、Mo、Sb年沉降通量较小，集中在0.08~0.39 mg/m²；Be、Co、Cd、Pb、Hg、Tl、Th、U的年沉降通量最小，集中在0.001~0.053 mg/m²。Al、Fe、Mn、Be、Th富集系数在0.32~3.05之间，这些金属元素主要来自自然来源；Cd与Hg富集系数分别为923.23、2511.47，达到严重富集的程度；其余金属元素富集系数在10~500之间，属中度富集。昌吉州境内煤炭资源丰富，近年煤炭开采量较大，城区供暖面积不断加大，供暖不断加强；市区车流量急剧增加，运输排放加剧；近郊及周边地区各类工业的分布等是各类金属元素在雪中富集的主要原因。冰雪节后冰灯拆除，降雪可有效捕集大气中的汞，冬季气温不利于Hg挥发等对Hg的严重富集也有重要影响。     

鞍山市大气尘和金属元素沉降通量及污染特征

通过采集鞍山市11个点位的降尘样品以及土壤样品,用ICP-MS分析了Cu、Mn、Zn、Pb等元素含量,并计算其沉降通量。结果表明,鞍山地区大气降尘的沉降通量为2.92～59.8g/(m2.month),其中鞍钢厂区沉降通量均值为31.6g/(m2.month),分别是周边地区和对照地区的4.72倍和10.5倍。重金属As、Cr、Pb和Cd的沉降通量分别为3.78、45.5、42.8、0.457g/(hm2.month)。降尘中各元素的富集系数为0.29～190,其中Cu、Fe、Zn、Mo、Cd、Pb和Se的富集系数大于10,说明这些元素主要来自于人为源。鞍钢厂区土壤中Cu、Pb、Mn、Zn、Mo、Cd、Ca、Fe和Se的含量较辽宁省土壤背景值高,说明其土壤环境已经受到了人类活动的影响。     

新疆大气氮沉降监测研究进展浅析

通过对新疆12个监测点氮沉降研究结果发现,无机活性氮浓度(p NH 4+、p NO 3-、NH 3、NO 2)在不同生态系统存在较大的时空差异,氮沉降通量变化随人为干扰程度呈递增趋势。总结了当前新疆大气氮沉降监测研究进展,包括主要监测方法、不同生态系统大气氮素干沉降的时空差异性分析、大气氮素干湿沉降通量估算。对大气氮素干湿沉降通量的整体估算、不同生态系统的监测常态化等还存在不足,未来评估氮沉降的综合气候效应、定量临界负荷以及生态系统对氮沉降通量急剧增加的响应是今后研究的重点方向。     

大气磷干沉降采样方法对比分析

以四川农业大学成都校区为监测点,采用大气主动采样法(AA)、大气干表面法(ADS)及大气湿表面法(AWS)3种常用干沉降采集方法做大气磷干沉降通量对比试验。结果表明,3种采样方法获得的大气磷干沉降通量间具有显著的差异性及相关性(P0.05),三者间可以进行换算统一;AA法适用于较短采样周期的连续性监测研究,ADS法适用于较长采样周期(5 d)的监测研究,而AWS法更适用于在长采样周期(月)内选取一段时间作为干沉降监测的研究。     

株洲夏季大气中气态总汞浓度特征

为研究株洲市夏季优良天气下大气中气态总汞(TGM)的浓度特征,于2013年8月利用大气汞分析仪(2537X,加拿大)进行了20 d的连续在线观测。结果显示,实验期间株洲市大气TGM的平均浓度为(4.20±3.37)ng/m3,中值浓度为3.40 ng/m3,高于背景地区和沿海城市,略低于国内其他重点城市。晴天、阴雨天TGM浓度分别为3.59、7.96 ng/m3。晴天TGM浓度具有一定日变化规律,最高值出现在早上7:00~9:00,之后逐渐降低,17:00出现最低值;TGM白天和夜间浓度分别为3.57、3.62 ng/m3,昼夜变化不大。晴天TGM与一次污染物SO2、CO、NO2具有显著的正相关性,与O3呈显著负相关性。株洲市夏季主导风向为东南风,该方向没有明显污染源,西北方向风向频率较低,但TGM浓度明显升高,其主要来源可能是位于西北方向的清水塘工业区。     

平顶山市大气PM10、PM2.5 污染调查

于2003年12月-2004年11月对平顶山市城区大气PM10、PM2.5污染进行了调查.结果表明,2004年大气PM10、PM2.5质量浓度分别为0.031 mg/m3～0.862 mg/m3、0.019 mg/m3～0.438 mg/m3;年均值分别为0.174 mg/m3、0.114 mg/m3,超标0.74倍、6.60倍.PM10、PM2.5污染的季节变化趋势是以冬季、春季高,秋季次之,夏季最低,细颗粒(PM2.5)约占PM10 65%;As、Pb、Cd、S、Zn、Cu、Mn、Ca等元素是颗粒物中主要污染元素,易在PM2.5中富集.平顶山市大气颗粒物污染的主要来源有煤炭燃烧、汽车尾气、城市基础建设和有色金属冶炼行业.     

2002—2012年京津唐PM10变化规律及差异

对2002年6月—2012年5月京津唐城市群大气可吸入颗粒物(PM10)质量浓度的长期监测数据进行分析,结合3市的地理、气候气象条件,分析了京津唐城市群大气颗粒物质量浓度的变化特征;根据3市PM10相互之间的发散系数,定量分析了3市PM10变化的差异。结果表明,2002—2012年北京市的PM10质量浓度变化范围为0.012~0.600 mg/m3,天津、唐山2市的PM10质量浓度变化范围分别为0.014~0.600、0.019~0.452 mg/m3。2008、2011年天津市PM10质量浓度年平均值达到二级标准,唐山市从2008年后PM10质量浓度年平均值达到二级标准;北京市PM10质量浓度总体变化趋势为春季秋季冬季夏季,天津、唐山市均为冬季春季秋季夏季,但不同年份的变化趋势略不同;北京-唐山、北京-天津、天津-唐山之间PM10的月度发散系数范围分别为0.402 7~0.159 2、0.406 8~0.142 9、0.323 1~0.107 8,说明空间距离最近的天津-唐山之间大气污染的相互影响较北京-天津、北京-唐山之间大。     

铅冶炼企业周边大气降尘中铅、镉、砷量及其对土壤的影响

通过在2012年5月-2013年4月1个周期年内，对修复基地和对照点每月大气降尘中铅、镉、砷沉降量的监测，结果表明：修复基地大气降尘中铅、镉、砷含量明显较对照点高，年总沉降量分别是对照点的17．6倍、16．3倍和14．1倍，表明铅冶炼企业对基地大气降尘中铅、镉、砷含量影响显著；大气降尘中铅、镉、砷沉降量受位置和时间影响较大，在相距不到100 m的测点间，沉降量相差1倍以上，冬季主导风明显、地面植被少、二次扬尘大，使处于铅冶炼企业下风向的基地降尘中铅、镉、砷沉降量较大。沉降量时空不均匀与土壤污染不均匀现状一致，也验证了铅冶炼企业是基地大气和土壤重金属污染的主要来源。以降尘缸模拟土壤进行测算，结果表明大气降尘中镉对土壤污染速度最快，风险最大。     

西安市区大气中PM2.5和PM10质量浓度污染特征

2013年3月—2014年2月期间,设置1个监测点位,采集了西安市区大气环境中PM10和PM2.5样品,采用重量法测定了PM2.5和PM10质量浓度。结果表明,西安市区PM2.5质量浓度为16~558μg/m3,平均值为128μg/m3,超标率69.1%;PM10质量浓度范围为32~887μg/m3,平均值为249μg/m3,超标率71.8%。虽然PM2.5和PM10质量浓度的逐日变化幅度比较大,但是整体变化趋势非常相似,存在显著的正相关关系(r=0.831 9)。PM2.5和PM10质量浓度存在明显的季节变化,均为冬季最高,春季次之,秋季较低,夏季最低。ρ(PM2.5)/ρ(PM10)为0.245~0.822,平均值为0.510,说明PM2.5在PM10中所占比例大于PM2.5~10;此外,该比值呈现一定的季节变化规律,冬季、夏季较高,秋季次之,春季最低。霾天气发生时,该比值和PM2.5质量浓度明显高于无霾天气。     

遵义市PM10中元素污染特征、来源与生态风险评价

采集2012年3月-2013年2月遵义市丁字口（市区点）、凤凰山（背景点）监测点的 PM10样品，并对 PM10中元素污染特征、来源和生态风险进行分析与评价。结果表明，遵义市 PM10质量浓度季节变化为：冬季＞春季＞秋季＞夏季，且市区点高于背景点，冬季超标率均为100％。PM10中 As、Pb、Hg、Mn质量浓度市区点高于背景点，且均为冬季最高。富集因子分析表明，Pb、As、Cd、Hg、Mn、Cu、Zn来自人为污染，生态危害顺序为：Cd＞Pb ＞As＞Cu ＞Zn ＞Ni ＞Cr，其中 Cd 的潜在生态危害为极强。     

长沙市大气中醛酮类化合物浓度变化特征

参照美国环保署EPA-TO11标准方法,于2014年7—10月监测了长沙市大气中醛酮类化合物的质量浓度。主要监测到的醛酮类化合物为甲醛、乙醛、丙酮、丙醛、甲基丙烯醛,夏季质量浓度最高的是甲醛(13.86 mg/m³),其次是乙醛(7.28 mg/m³)、丙酮(7.14 mg/m³),秋季质量浓度最高的是甲醛(10.31 mg/m³),其次是丙酮(8.37 mg/m³)、乙醛(5.78 mg/m³)。夏季醛酮类化合物的总量高于秋季,甲醛、乙醛、丙酮的质量浓度最大值基本出现在13:00—15:00。C1/C2(甲醛/乙醛)、C2/C3(乙醛/丙醛)的平均值分别为2.02、10.19。分析了醛酮类化合物之间的相关性以及它们可能的来源。丙醛和甲醛、乙醛的相关性较好,三者有共同的人为来源。夏季大气中除丙酮外,其他醛酮类化合物的相关性均较好。夏季甲基丙烯醛和甲醛、乙醛、丙酮有相同的自然来源。综合分析可知,长沙大气中醛酮类化合物质量浓度受自然因素和人为因素的双重影响。     

Air quality and deposition of trace elements in Didouche Mourad, Algeria

Total suspended particulate matter and deposition fluxes of particles were investigated in the town of Didouche Mourad which is located 13 km north of Constantine. Samples of air particulate matter were collected at one site located in the heart of the town and situated 3 km north of a cement plant. Samples were collected from 2 November 2002 to 28 April 2003 every 3 days using a high volume air sampler. Sampling intervals were 24 h in all cases. During the same period, samples of dust fallout were collected at the same site. Samples were collected at 30-day intervals. Lead, chromium, manganese, nickel, copper, cobalt and cadmium deposition fluxes were measured and both the soluble and insoluble fractions were determined. Furthermore, the information gathered by this study was correlated with the corresponding hourly weather data provided by a weather station installed at the study station. The possible sources for dust and trace metals were analyzed by comparing average contributions of wind aspects to the concentrations and depositions of mass and chemical species with the average frequencies of wind direction. The mean concentration was 300 μg/m³. The average dust deposition rate through the period of study was 221 mg/(m².day). Results indicate that anthropogenic sources contribute greatly to trace elements. An exposure assessment to the heavy metals taking into account the inhalation route and soil dust ingestion was carried out and allowed direct comparison of trace metal intakes via these routes.     

Heavy metal concentration in deepwater rose shrimp species (Parapenaeus longirostris,Lucas, 1846) collected from the Marmara Sea Coast in Tekirdağ

Zn, Cd, Cr, Hg, As (total), Cu, Pb, and Ni levels of the deepwater rose shrimp (Parapenaeus longirostris, Lucas 1846), which were collected from the Tekirda? coast of the Marmara Sea, were evaluated. The Marmara Sea is the recipient of discharges from both land-based sources and the Black Sea Bosphorus stream. There are large numbers of anthropogenic activities in the coastal region of the northern Marmara Sea that include urban effluent, discharges from touristic resorts, agricultural runoff, fishing, and transportation. Heavy metal contamination of water resources may cause critical health problems for the people living around these water bodies. In deepwater rose shrimp (P. longirostris), the highest concentration level detected for Zn was 22.4?±?24.4 mg/kg in winter 2012, Cd 0.106?±?0.01 mg/kg in summer 2012, Cr 0.77?±?0.05 mg/kg in winter 2012, Hg 0.18?±?0.04 mg/kg in summer 2011, As 9.93?±?1.4 mg/kg in spring 2012, Cu 25.48?±?0.3 mg/kg in winter 2012, Pb 2.12?±?0.8 mg/kg in spring, and Ni 19.25?±?7.1 mg/kg in spring. The values of heavy metal analysis were compared to both the Turkish Food Codex (TFC) limits and international standards for human consumption. The Pb, As, and Cu levels were found to be higher than the maximum allowable limits.     

北京市大气气态汞变化特征

采用Tekran 2537X大气汞分析仪在线测量北京市城区大气中气态元素汞(GEM,简称大气汞) 浓度,研究大气汞浓度随不同气象条件的变化特征。通过分析2016年10月—2017年9月大气汞监测数据发现,该监测点全年大气汞浓度为0.48～16.25 ng/m³,均值为(3.41±1.79)ng/m³。春季、夏季、秋季和冬季大气汞浓度均值依次为2.93 、2.95、4.27、3.37 ng/m³,其中,秋季大气汞浓度明显高于其他季节 。秋季大气汞浓度显著偏高可能由不利的大气扩散条件导致。大气汞夜间浓度显著高于白天浓度。同时,将大气汞与SO₂、CO及PM_2.5进行相关性分析,发现大气汞浓度变化趋势与SO₂、CO和PM_2.5呈显著正相关。结合风向和风速进行污染来源分析,得到该点位大气汞在西南和东北方向上受人为排放源影响较大。污染源类型分析表明,冬季大气汞与CO同源性强,主要来自本地供暖用煤。     

Atmospheric deposition of major and trace elements in Amman, Jordan

Wet and dry deposition samples were collected in the capital of Jordan, Amman. Concentrations of Al, Ba, Bi, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, Sb, V, Zn, Fe, Sr, Mg²⁺, Ca²⁺, Na⁺, K⁺, Cl⁻, NO₃ ⁻ and SO₄ ²⁻, along with pH were determined in collected samples. Mean trace metal concentrations were similar or less than those reported for other urban regions worldwide, while concentrations of Ca²⁺ and SO₄ ²⁻ were among the highest. High Ca²⁺ concentrations were attributed to the calcareous nature of the local soil and to the influence of the Saharan dust. However, high SO₄ ²⁻ concentrations were attributed to the influence of both anthropogenic and natural sources. Except for Cl⁻, NO₃ ⁻, SO₄ ²⁻ and Cu, monthly dry deposition fluxes of all measured species were higher than wet deposition fluxes. The annual wet deposition fluxes of trace metals were much lower than those reported for other urban areas worldwide.     

Characterisation of particulate matter emissions from the Zimbabwe Mining and Smelting Company (ZIMASCO) Kwekwe Division (Zimbabwe): a ferrochrome smelter

Particulate matter emissions from stack number 2 of a majorferrochrome smelter, Zimbabwe Mining and Smelting Company(ZIMASCO) were characterized and the rates at which the elementsCr, Fe, Cu and Zn and total ferrochrome dust are emitted into theatmosphere were determined. The extent of soil contamination bythe dust deposited around the smelter in the generally prevailingsoutheasterly wind direction around the smelter was carried out.The highest concentrations of Cr and Fe occurred in the fineparticulates of sizes less than 59 m whilst that of Cu and Znoccurred in the coarse particulates of size range 70-100 m.The emission rates from stack 2 were; total ferrochromeparticulates 62.17 kg h^-1, Cr 6.217 kg h^-1, Fe 2.423 kg h^-1, Zn42 mg h^-1 and 6 mg h^-1 for Cu. Particulate matter was emitted at arate of 289 mg m^-3 from stack number 2. This value exceeds thelegal limit of 200 mg m^-3. Chromium and iron are the metalsin the largest amounts. The particles that constitute the largestproportion of the dust were in the range of 58-107.5 m. Thisis a characteristic feature of the particulate matter emissionsfrom ZIMASCO. Soils in the downwind direction from the smelterwere polluted with Cr up to a distance of about 700 m outward fromthe perimeter of the boundary of the smelter.     

Contributions of dry and wet depositions of polychlorinated dibenzo-p-dioxins and dibenzofurans to a contaminated site resulting from a penetachlorophenol manufacturing process

The soils at a factory for manufacturing pentachlorophenol were heavily contaminated by polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). In order to verify the contributions of dry and wet deposition of PCDD/Fs from the ambient air, the concentration of PCDD/Fs in ambient air and soil were measured, the partition of particle- and gas-phases of atmospheric PCDD/Fs was calculated, and the annual fluxes of total dry and wet PCDD/F depositions were modeled. Average atmospheric PCDD/F concentration was 1.24 ng Nm^???3 (or 0.0397 ng I-TEQ Nm^???3). Moreover, over 92.8% of total PCDD/Fs were in the particle phase, and the dominant species were high chlorinated congeners. The total PCDD/F fluxes of dry and wet deposition were 119.5 ng m^???2 year^???1 (1.34 ng I-TEQ m^???2 year^???1) and 82.0 ng m^???2 year^???1 (1.07 ng I-TEQ m^???2 year^???1), respectively. By scenario simulation, the total fluxes of dry and wet PCDD/F depositions were 87.1 and 68.6 ng I-TEQ, respectively. However, the estimated PCDD/F contents in the contaminated soil were 839.9 ?? g I-TEQ. Hence, the contributions of total depositions of atmospheric PCDD/F were only 0.02%. The results indicated that the major sources of PCDD/F for the contaminated soil could be attributed to the pentachlorophenol manufacturing process.     

Characteristic Study of Dry Deposition, Concentration, Compositions for Particulates Mass and Ionic Species During Summer and Autumn Season at a Traffic Sampling Site

Aerosol samples for dry deposition and total suspend particulates (TSP) were collected from August to November of 2003 in central Taiwan. Ion chromatography was used to analyze the related water-soluble ionic species (Cl⁻, NO₃ ⁻, SO₄ ²⁻, Na⁺, NH₄ ⁺, K⁺, Mg²⁺ and Ca²⁺). The results obtained in this study indicated that the ambient air particulate mass concentrations in the daytime period (averaged 975.4 μg m⁻³) were higher than the nighttime period (averaged 542.1 μg m⁻³). And the daytime dry deposition fluxes (averaged 58.12 μg m⁻² sec⁻¹) were about 2.2 times as that of nighttime dry deposition fluxes (averaged 26.54 μg m⁻² sec⁻¹) of the downward dry deposition. The average values downward and upward of dry deposition fluxes for the weekend period were almost higher than the weekday period for either daytime or nighttime period. Furthermore, the average daytime dry deposition fluxes (averaged 26.37 μg m⁻² sec⁻¹) were also about 2.3 times as that of nighttime dry deposition fluxes (averaged 11.52 μg m⁻² sec⁻¹). Moreover, the results also indicate that SO₄ ²⁻ and Ca²⁺ have higher average composition for total suspended particulates in the daytime period while Ca²⁺, SO₄ ²⁻, and Na⁺ have the higher average composition for total suspends particulates in the nighttime period.     

西宁市非采暖季和采暖季PM2.5中14种金属元素特征

于2012年11月采暖季和2013年9月非采暖季,在青藏高原典型城市西宁市4个采样点采集细颗粒物(PM_(2.5))样品,共获得40个有效样品。用微波消解-ICP-MS法、原子荧光法分析了样品中14种重点防控金属。结果表明:14种重点防控金属中Ag、Tl平均质量浓度为0.10~0.50 ng/m~3,Co、Sb、Hg平均质量浓度为0.50~4.00 ng/m~3,V、Cd、Cr、Ni、Cu、As平均质量浓度为4.00~50.0 ng/m~3,Mn、Pb、Zn平均质量浓度为50.0~2 000 ng/m~3。采样期间,采暖季相比非采暖季,PM_(2.5)质量浓度有下降趋势,不同采样区金属元素浓度有增有减。富集因子分析结果表明,重点防控金属元素在非采暖季主要来源于土壤风沙扬尘、机动车尾气和工业排放,采暖季主要来源于土壤风沙扬尘、燃煤、燃油、机动车尾气和工业排放。非采暖季Zn、Ag、Cd、Hg、Tl和Pb富集因子较高,采暖季Zn、As、Ag、Cd、Sb、Hg、Tl、Pb富集因子较高,更容易受到人为源的影响。