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1.
大气细粒子(PM2.5)污染是全球尤其是我国许多城市的重要环境问题。利用示踪物质识别和估算大气颗粒物来源是公认的可靠技术,纤维素可以作为示踪物质表征一次颗粒物的天然植被排放来源。本文针对大气细粒子中纤维素含量低、全程序空白相对较高等难点,优化建立了纤维素酶水解、GOD-苯酚-四氨基安替比林测糖法,在我国首次应用于测定大气PM2.5中纤维素的含量,估算天然植被排放源的贡献。方法检出限为0.26 μg/m3(纤维素),可以满足大气PM2.5纤维素测定要求;而且有效地降低了空白,全程序空白值(36.5 μg葡萄糖)低于文献方法空白值(53.8 μg葡萄糖),使之更适合于PM2.5的测定。使用本方法对2012年5月至6月采集的北京市大气PM2.5样品进行分析,纤维素检出率为96%,纤维素的平均含量为(0.573±0.17) μg/m3,折合为天然植被排放量占PM2.5质量浓度的1.37%±0.65%;天然植被排放源对有机碳的平均贡献率为4.4%,最大达到9.2%,反映出天然植被排放是北京市PM2.5的重要来源之 一。本研究方法为我国城市大气颗粒物(包括总悬浮颗粒物、PM10、PM2.5等)来源识别提供了新的手段。  相似文献   

2.
为了深入探讨黔南地区早石炭世黑色岩系沉积-构造环境,笔者对页岩气钻孔CY1井打屋坝组黑色岩系进行了详细采样测试,并重点分析了页岩稀土元素地球化学特征。分析结果表明,该区早石炭世页岩稀土元素总量(ΣREE)为(213.08~308.1)×10-6,平均值为251.43×10-6,大于北美页岩的平均值(173. 21×10-6);w(ΣLREE)/w(ΣHREE)及w(Ce)N/w(Yb)N等地球化学参数表明,轻、重稀土元素分异明显;REE分布模式呈平坦状,表现出轻稀土富集、重稀土元素亏损;δEu值为0.53~0.67 < 1,显示中等程度的负Eu异常,Ce异常表现不明显。根据δCe和Ce异常值的变化,反映研究区早石炭世为缺氧还原环境。根据稀土元素组合特征、δEu值的变化及w(La)N/w(Yb)N-ΣREE的图解特征,结合区域地质背景,认为黔南地区打屋坝组黑色页岩的物源来自黔中隆起和雪峰山隆起,母岩为沉积岩和花岗岩的混合,沉积区构造环境为被动大陆边缘构造背景。  相似文献   

3.
西准噶尔巴音达拉地区发育一套酸性火山岩,被称为卡拉岗组,岩石组合以流纹岩、英安岩、流纹质熔结凝灰岩等酸性火山岩为主。本文对卡拉岗组火山岩进行高精度锆石LA-ICP-MS U-Pb测年,获得英安岩和流纹岩的加权平均206Pb/238U年龄分别为（294.4±1.3）Ma（n=9,MSWD=0.8）和（298.4±2.5）Ma（n=9,MSWD=3.4）,其形成于早二叠世。岩石地球化学特征表明,卡拉岗组火山岩岩具有高硅（66.69%~75.21%）,富碱（Na2O+K2O：6.98%~8.35%）,低MgO（0.18%~1.32%）,贫钙（0.24%~2.49%）的特征,均属过铝质（A/CNK：1.14~1.33）及高钾钙碱性系列。微量元素数据显示,稀土总量为∑REE为83.82×10-6~197.61×10-6,（La/Yb）N=3.15~12.50,轻、重稀土元素分馏比较明显,轻稀土元素（LREE）较为富集,重稀土元素分布相对平坦,球粒陨石标准化配分模式为右倾型。微量元素富集大离子亲石元素（LILE）Rb、Th、U、K,并亏损高场强元素（HFSE）Nb、Ta、P、Ti。综合最新区域资料及本文研究成果,文章认为研究区早二叠世卡拉岗组火山岩岩浆来源于壳源物质不同程度的部分熔融,残留相中有少量斜长石和角闪石,为后碰撞伸展阶段的产物。  相似文献   

4.
内蒙古边家大院锡多金属矿床是大兴安岭南段多金属成矿带的代表性矿床之一,其西矿区主要发育斑岩型Sn-Cu-Mo矿体,矿体发育于石英斑岩体内。文章通过对石英斑岩开展全岩地球化学、锆石Hf同位素以及锆石微量元素地球化学分析研究,确定了该含矿岩体岩浆性质、来源及演化历史,探讨了成岩成矿关系,并进一步评估了该岩体成锡、铜矿潜力。研究表明,边家大院石英斑岩为准铝质-弱过铝质,高钾钙碱性花岗岩。稀土元素具有轻稀土元素富集、重稀土元素亏损,Eu负异常明显的特征。微量元素具有富集大离子亲石元素,亏损高场强元素的特征。结合其较低的Zr/Hf和Nb/Ta比值以及较高的Rb/Sr比值判断其经历了高分异结晶演化。根据锆石微量元素地球化学特征,确定边家大院石英斑岩源于还原性（ΔFMQ-0.15）、高温贫水（> 750oC）岩浆。边家大院石英斑岩εHf（t）为-0.86~5.99,TDM2=809~1240 Ma,为中元古代-新元古代年轻地壳部分熔融形成。根据锆石微量元素Ce4+/Ce3+,CeN/CeN*,Ce/Nd和EuN/EuN*指针性比值及岩浆特性判断,该石英斑岩有利于锡金属富集成矿,而成铜钼矿潜力小。  相似文献   

5.
为了研究祁连山大雪山地区大气PM2.5细粒子中可溶性无机离子组分的变化特征, 于2010年7月至2011年7月在祁连山冰川与生态环境综合观测站附近采集46个大气PM2.5的Telfon滤膜样品, 并应用离子色谱对可溶性离子进行了分析.结果显示: 所测样品的阴、 阳离子中, SO42-、 NO-3、 Ca2+和NH+4的质量浓度分别为1.54μg·m-3、 0.38μg·m-3、 0.73μg·m-3和0.22μg·m-3, 累计约占到水溶性离子总量的88%.可溶性离子浓度呈现出春夏季节明显高于秋冬季节的特征, 夏季的浓度最高, 其次是春季、 冬季和秋季. Cl-、 Ca2+、 Na+和Mg2+之间的相关性极高, SO42-和NO-3与大部分阳离子的相关性都很高, 说明大部分硫酸盐是来自于中亚沙尘源区的自然源, 而并非是通过人类活动造成的一次污染物通过二次反应过程得到的. NH+4仅与SO42-通过相关性检验说明, 该地区NH3主要中和了大气中硫酸并生成(NH4)2SO4.该地区的大气环境主要来源于自然源的影响, 但夏季风期间人为污染排放已经不可忽视, 这也得到HYSPLIT后向轨迹模式的计算验证.  相似文献   

6.
安林地区铁矿属典型的接触交代型铁矿，与成矿作用有关的岩浆岩为燕山期闪长岩，奥陶系马家沟组第三岩性段是主要的赋矿地层。通过对该矿区与成矿相关的岩矿石稀土元素地球化学研究表明：闪长岩w（ΣREE）平均=114.12×10-6，灰岩w（ΣREE）平均=11.98×10-6，磁铁矿石w（ΣREE）平均=26.13×10-6，矽卡岩w（ΣREE）平均=65.67×10-6，磁铁矿石和矽卡岩的稀土总量介于闪长岩与灰岩之间；稀土配分曲线总体上都表现为轻稀土相对富集的右倾型；闪长岩一般具有极弱的正Eu异常，灰岩具有较明显的负Eu异常，矽卡岩具有较弱的负Eu异常，磁铁矿石具弱的正Eu异常或Eu异常不明显；岩矿石的δCe值非常接近，且均不显示或显示极弱的负Ce异常；铁矿石和矽卡岩继承了来自闪长岩和灰岩的稀土元素特征，结合S、Pb同位素特征，认为闪长岩提供了主要成矿物质，赋矿地层也可能提供了部分成矿物质。  相似文献   

7.
新疆东天山葫芦岩体岩石学与地球化学研究   总被引：13，自引：3，他引：10  
葫芦岩体位于康古尔—黄山韧性剪切带东段,地表出露面积0.75km2。主要岩石类型有辉长闪长岩、辉长岩、辉石岩、辉橄岩、橄揽岩。岩相之间多呈渐变过渡关系,局部也有侵入接触。主量元素化学组成基本上属拉斑玄武岩系列。岩石相对富集LREE、适度亏损高场强元素(Nb、Ta、Ti)。岩浆演化过程中发生了较弱的同化混染作用。橄榄石、斜方辉石、单斜辉石和斜长石的分离结晶作用是岩浆演化的主要机制。四件样品εNd(t)值(＋6.4~+7.1),一件样品的εSr(t)=+3.4,其余三件的εSr(t)值(-10.1~-9.3),206Pb/204Pb(18.091~18.513)、207Pb/204Pb(15.459~15.528)、208Pb/204Pb(37.526~38.126)。元素地球化学和Nd、Sr、Pb同位素体系表明,源区软流圈来源的岩浆中混入了富集岩石圈地幔来源的岩浆。稀土元素地球化学证明,熔融作用发生于尖晶石稳定域内。由此可见,岩体是尖晶石稳定域内占主体的软流圈地幔与富集岩石圈地幔相互作用的结果。  相似文献   

8.
栖霞牙山花岗岩体形成于中生代早白垩世（118 Ma）,其岩石类型以花岗岩和花岗闪长岩为主,岩体中发育大量的暗色闪长质微粒包体。通过对牙山花岗岩及其暗色包体地球化学特征研究表明,包体围岩w（SiO2）=65.5%~68.82%,铝饱和度（A/CNK）为0.89~1.03<1.1,为准铝质钙碱性Ⅰ型花岗岩;暗色包体具有较低w（SiO2）值（54.82%~60.89%）、高w（TFe2O3）值（6.11%~8.15%）、高w（MgO）值（3.57%~5.19%）的特征。稀土元素配分模式图显示二者皆为轻稀土富集的右倾型曲线,微量元素蛛网图中二者均表现为富集Ba、K等大离子亲石元素,亏损Ta、Nb、Ti等高场强元素,具有大陆地壳的特征。暗色包体与寄主岩石的Sr同位素初始比值（87Sr/86Sr）i分别为0.709 29~0.709 58和0.709 21~0.709 71,应为同源岩浆的产物。两阶段Nd模式年龄（T2DM）分为2 291 Ma-2 391 Ma和2 208 Ma-2 353 Ma,表明可能是古元古界陆壳物质部分熔融的产物。Pb同位素特征显示牙山岩体的原始岩浆以下地壳为主,w（Nb）/w（Ta）值介于下地壳与原始地幔之间,表明可能受到幔源物质的影响,包体中大量磷灰石呈针状结晶状态,进一步暗示存在岩浆混合作用。综上并结合区域构造背景认为,牙山岩体为早白垩世中晚期起源于火山弧环境的壳源特征花岗岩,形成过程中存在幔源物质的加入,它的形成与太平洋板块的俯冲作用密切相关。  相似文献   

9.
陆内强碱性火山岩的成因：以山东无棣大山霞石岩为例   总被引：2，自引：0，他引：2  
罗丹  陈立辉  曾罡 《岩石学报》2009,25(2):311-319
本文以山东无棣的大山更新世霞石岩为例,通过全岩的元素地球化学和Sr-Nd-Hf同位素组成特征,探讨陆内强碱性幔源火山岩的成因及其源区特征。山东地区的新生代玄武岩主要分为早晚两期,早期以橄榄玄武岩为主,晚期以强碱性岩为主（包括霞石岩、碧玄岩等,常见地幔橄榄岩捕掳体）。大山霞石岩为晚期火山作用的代表,具有富碱和贫硅铝等强碱性火山岩的典型特征。在微量元素组成上,大山霞石岩以强烈富集轻稀土元素和大离子亲石元素,在原始地幔标准化图上以明显亏损Zr、Hf、Ti为特征(Hf/Hf*=0.66~0.68,Ti/Ti*=0.68~0.70)。其Sr-Nd-Hf同位素比值均一(87Sr/86Sr>=0.70333~0.70339,εNd=5.95~6.34,εHf>=8.26~8.43),与早期玄武岩组成一个两端元混合的排列,其中大山霞石岩位于亏损端元一侧。在同位素组成相同的情况下,大山霞石岩相对山东新生代早期玄武岩具有明显偏低的Hf/Sm、Hf/Hf*、Ti/Ti*比值,说明源区残留矿物组合可以造成高场强元素Zr、Hf、Ti与稀土元素之间的明显分馏,暗示源区存在非橄榄岩组分。大山霞石岩相对橄榄岩来源熔体偏低的CaO含量和偏高的Zr/Hf比(47.9~48.4),说明其源区残留过剩的单斜辉石,源岩中的非橄榄岩成分为辉石岩或角闪石岩。中等亏损的同位素组成特征说明这些非橄榄岩组分可能与该区显生宙的地壳重循环过程有关。  相似文献   

10.
准噶尔盆地陆东—五彩湾地区石炭系火山岩位于上石炭统巴塔玛依内山组地层中,主要为玄武岩、玄武质安山岩和安山岩,基本属于钙碱性系列。火山岩的Mg#介于38~57之间,全碱含量较高K2O＋Na2O为4.75%~6.16％）,TiO2的含量（0.96%~2.04％）和Na2O/K2O比值（均大于2）较高,轻稀土元素（LREE）相对重稀土元素（HREE）富集（(La/Yb)N=2.4~4.7）,同时显示有轻微的重稀土分馏（(Gd/Yb)N=1.5~1.8）,无明显的Ce异常,大部分样品具有轻微的Eu负异常（δEu＝0.89~1.05）,大离子亲石元素（LILE）相对高场强元素（HFSE）富集,Nb、Ta相对于LREE和LILE明显亏损,La/Nb比值为2.0~2.8,Th/La比值（≈0.1）较低,Zr/Y比值（3.95~7.03）较高。火山岩(87Sr/86Sr) i＝0.70278~0.70365,εNd(t)＝＋5.69 ~ ＋8.24,tDM为0.47~0.67Ga。这些特征连同相关判别图解一起表明,这套火山岩不是形成于典型的板内或岛弧环境,而是形成于后碰撞期伸展背景下,是软流圈物质上涌发生部分熔融、产生的岩浆在上升和侵位的过程中受到了晚石炭世之前弧组分混染的产物。其所携带的弧岩浆特征继承自混染的碰撞前的弧组分。  相似文献   

11.
分析了2014~2018年北方5个典型中小盆地城市(兰州、银川、临汾、太原、南阳)PM10与PM2.5的浓度变化特征和大致来源类型。除2018年银川PM2.5浓度外,各市PM10和PM2.5年均浓度均超标;兰州、银川和南阳PM10与PM2.5呈逐年下降趋势,南阳下降最明显;临汾PM10与PM2.5呈逐年上升趋势;太原PM10与PM2.5稳定维持在一个高浓度状态。5个城市颗粒物浓度的季节变化特征一致:冬春高、夏秋低。对PM2.5/PM10值而言,冬季和夏季该比值较高,分别受取暖和降水的影响;春季和秋季该比值较低,分别受沙尘和秸秆焚烧及高强度建筑施工的影响。5市PM2.5和PM10浓度具有良好的线性关系,细颗粒占比大小顺序为临汾>南阳>太原>银川>兰州。  相似文献   

12.
Size distribution of PM10 mass aerosols and its ionic characteristics were studied for 2 years from January 2006 to December 2007 at central Delhi by employing an 8-stage Andersen Cascade Impactor sampler. The mass of fine (PM2.5) and coarse (PM10?2.5) mode particles were integrated from particle mass determined in different stages. Average concentrations of mass PM10 and PM2.5 were observed to be 306 ± 182 and 136 ± 84 μg m?3, respectively, which are far in excess of annual averages stipulated by the Indian National Ambient Air Quality Standards (PM10: 60 μg m?3 and PM2.5: 40 μg m?3). The highest concentrations of PM10?2.5 (coarse) and PM2.5 (fine) were observed 505 ± 44 and 368 ± 61 μg m?3, respectively, during summer (June 2006) period, whereas the lower concentrations of PM10?2.5 (35 ± 9 μg m?3) and PM2.5 (29 ± 13 μg m?3) were observed during monsoon (September 2007). In summer, because of frequent dust storms, coarse particles are more dominant than fine particles during study period. However, during winter, the PM2.5 contribution became more pronounced as compared to summer probably due to enhanced emissions from anthropogenic activities, burning of biofuels/biomass and other human activities. A high ratio (0.58) of PM2.5/PM10 was observed during winter and low (0.24) during monsoon. A strong correlation between PM10 and PM2.5 (r 2 = 0.93) was observed, indicating that variation in PM10 mass is governed by the variation in PM2.5. Major cations (NH4 +, Na+, K+, Ca2+ and Mg2+) and anions (F?, Cl?, SO4 2? and NO3 ?) were analyzed along with pH. Average concentrations of SO4 2? and NO3 ? were observed to be 12.93 ± 0.98 and 10.33 ± 1.10 μg m?3, respectively. Significant correlation between SO4 2? and NO3 ? in PM1.0 was observed indicating the major sources of secondary aerosol which may be from thermal power plants located in the southeast and incomplete combustion by vehicular exhaust. A good correlation among secondary species (NH+, NO3 ? and SO4 2?) suggests that most of NH4 + is in the form of ammonium sulfate and ammonium nitrate in the atmosphere. During winter, the concentration of Ca2+ was also higher; it may be due to entrainment of roadside dust particles, traffic activities and low temperature. The molar ratio (1.39) between Cl? and Na+ was observed to be close to that of seawater (1.16). The presence of higher Cl? during winter is due to western disturbances and probably local emission of Cl? due to fabric bleaching activity in a number of export garment factories in the proximity of the sampling site.  相似文献   

13.
运用电感耦合等离子体质谱和煤质分析等技术方法,对内蒙古胜利煤田0-1号钻孔揭露的早白垩世1、2和4号煤层(共20个煤分层,1个夹矸)进行了研究。结果显示,1、2号煤层的挥发分产率大于44%,透光率小于50%,煤类为褐煤;4号煤层挥发分产率42%,透光率53%,煤类为次烟煤(长焰煤);1、2号煤层灰分和硫含量较高,4号煤层灰分和硫含量较低。与世界煤微量元素含量平均值相比,1、2和4号煤层中Sb富集,V、Zr、Nb、Hf、W等元素轻微富集,其它微量元素的含量接近或低于世界煤含量的平均值。1、2和4号煤层中稀土元素和钇(REY)含量较低,根据上地壳标准值(La/Lu)N比值,所有煤分层均显示重稀土富集类型特征,而煤中泥岩夹矸则显示轻稀土富集类型特征。  相似文献   

14.
Ambient air and coarse, fine and particulate-bound mercury (Hg(p)) pollutants were collected and analyzed from March 17 to May 22 and September 3, 2009 to March 5, 2010 at a highway traffic site located in Sha-Lu, central Taiwan. This study has the following objectives: (1) to measure the coarse and fine particulates concentrations and the particulate-bound mercury Hg(p) which was attached to these particulate; (2) to determine the average Hg(p) compositions in coarse and fine particulates and (3) to compare the Hg(p) concentrations and compositions particulate in this study to the those obtained in other studies. The results obtained in this study indicated that the average ambient air PM2.5, PM2.5–10 and PM10 were 18.79 ± 6.71, 11.22 ± 4.93 and 30.01 ± 10.27 μg/m3, respectively. The ranges of concentrations for Hg(p) in PM2.5 were from 0.0016 to 0.0557 ng/m3, from 0.0006 to 0.0364 ng/m3 in PM2.5–10 and from 0.0022 to 0.0862 ng/m3 in PM10. In addition, the highest particle-bound mercury compositions in PM2.5 were 16.85 ng/g and the lowest particle-bound mercury concentrations were 0.55 ng/g. The highest particle-bound mercury compositions in PM2.5–10 were 13.88 ng/g and the lowest particle-bound mercury in PM2.5–10 were 0.22 ng/g.  相似文献   

15.
新兴关键矿产——三稀（稀有、稀土、稀散）金属是支撑国家“十四五、十五五”节能环保、新一代信息技术、生物、高端装备制造、新材料、新能源以及新能源汽车7大战略性新兴产业发展的关键矿产资源。四川省三稀金属矿产资源非常丰富。但以往对三稀资源重视不够,资源家底不清,相关成矿作用的研究较为粗浅。笔者在总结三稀资源分布特点、分析研究成矿地质背景、典型矿床以及元素富集规律的基础上,估算了17种三稀金属的资源量,预测了资源潜力,提出四川进一步找矿勘查方向。  相似文献   

16.
Major and trace elements including rare earth elements (REEs) chemistry of the metapelitic rocks of Bulfat Complex (Iraqi Zagros Suture Zone) indicate their enrichment in large-ion Lithophile, light rare earth (LREE) elements, and relative depletion of high field strength and heavy rare earth (HREE) elements. The linear correlation coefficients between TiO2, K2O, and Al2O3 and total REE reveal that phyllosilicates (e.g., mica) and accessory minerals mainly Ti-bearing phases (e.g., ilmenite) are likely the dominant hosts for REEs. Chondrite-normalized REE patterns typical of continental margin settings with significant enrichment of LREE, prominent negative Eu anomalies, and nearly flat HREE are positively correlated with post-Archean Australian shale (PAAS) and upper continental crust (UCC) patterns. Additionally, their consistent elemental La/Sc, Th/Sc, La/Co, Th/Co, Cr/Th, and Eu/Eu* values suggest that sediments may have been originally derived from an old post-Archean upper continental crust composed chiefly of granitic component. It seems most likely that the felsic source rocks were originated by a process of intra-crustal differentiation such as partial melting and/or fractional crystallization involving fractionation of Ca-plagioclase. The geochemical evidences particularly REEs evaluation show that deposition of clasts occurred in an active continental margin setting during lower–upper Cretaceous period contemporaneous with the igneous activities. It is evident therefore that the clasts source is from the north–northeast side, i.e., from the active margin of Iranian microcontinent (Sanandaj–Sirjan Zone).  相似文献   

17.
The major, trace and rare earth elements geochemistry and clay mineral compositions in the river bed sediments from lower reaches of Godavari river suggest that they are derived from weathering of felsic rocks. Trace and rare earth elemental compositions indicate evidence of sedimentary sorting during transportation and deposition. Lower concentrations of transition elements, such as V, Ni and Cr imply enrichment of felsic minerals in these bed sediments. The REE pattern in lower Godavari sediments is influenced by the degree of source rock weathering. The light rare earth elements (LREE) content are indicating greater fractionation compared to the heavy rare earth elements (HREE). A striking relationship is observed between TiO2 and gZREE content suggesting a strong control by LREE-enriched titaniferous minerals on REE chemistry. Shale-normalized REE pattern demonstrate a positive Eu anomaly, suggesting weathering of feldspar and their secondary products, which are enriched in Eu. Chondrite-normalised REE pattern is characteristic of felsic volcanic, granites and gnessic source rocks. Trace elemental compositions in sediments located near urban areas suggest influence of anthropogenic activity. Chemical Index of Alteration (CIA) is high (avg. 65.76), suggesting a moderate chemical weathering environment. X-ray diffraction analysis of clay fraction shows predominance of clay minerals that are formed because of the chemical weathering of felsic rocks.  相似文献   

18.
Given the relevance of desert aerosols to environmental issues such as dust storms, climate change and human health effects, we provide a demonstration of how the bedrock geology of an arid area influences the mineralogy and geochemistry of even the finest particulate matter (i.e., the inhalable fraction <10 μm in size: PM10). PM10 samples extracted from desert sediments at geologically contrasting off-road sites in central and southeastern Australia (granitic, high grade metamorphic, quartzitic sandstone) were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS). The “granitic” PM10 are highly alkali feldspathic and illitic, with a wide range of accessory minerals including rutile (TiO2), monazite [(Ce, La, Nd, Th, Y) PO4], xenotime (YPO4), apatite [Ca5(PO4)3 (F, OH, Cl)], hematite (Fe3O4), zircon (ZrSiO4) and thorite (ThSiO4). This mineralogy is reflected in the geochemistry which shows notable enrichments in rare earth elements (REE) and most high field strength elements (both held in the accessory minerals), and higher than normal levels of low (<2.0) ionic potential elements (Na, K, Li, Cs, Rb: held in alkali feldspar and illite). The “metamorphic” resuspended PM10 define a mineralogy clearly influenced by local exposures of pelitic and calc-silicate schists (sillimanite, muscovite, calcite, Ca-amphibole), a dominance of monazite over other REE-bearing phases, and a geochemistry distinguished by enrichments in alkaline earth metals (Ca, Mg, Ba, Sr) and depletion in heavy REE. The “quartzite” PM10, derived from rocks already recycled by Precambrian erosion and sedimentary transport, show a sedimentologically mature mineralogy of mostly quartz and kaolinite, detrital accessory ilmenite, rutile, monazite and hematite, and the strongest geochemical depletion (especially K, Rb, Cs, Na, Ca, Mg, Ba).  相似文献   

19.
The objective of the study is to investigate spatio-temporal variations of PM10, PM2.5, and PM1 concentrations at seven residential sites, located in the vicinity of opencast coal projects, Basundhara Garjanbahal Area (BGA), India. Meteorological parameters such as wind speed, wind direction, relative humidity, and temperature were collected simultaneously with PM concentrations. Mean concentrations of PM10 in the range 215 ± 169–526 ± 412 μg m?3, PM2.5 in the range of 91 ± 79–297 ± 107 μg m?3, PM1 in the range of 68 ± 60–247 ± 84 μg m?3 were obtained. Coarse fractions (PM2.5–10) varied from 27 to 58% whereas fine fractions (PM1–2.5 and PM1) varied in the range of 51–73%. PM2.5 concentration was 41–74% of PM10 concentration, PM1 concentration was 31–62% of PM10 concentration, and PM1 concentration was 73–83% of PM2.5 concentration. Role of meteorology on PM concentrations was assessed using correlation analysis. Linear relationships were established among PM concentrations using least square regression analysis. With the aid of principal component analysis, two components were drawn out of eight variables, which represent more than 75% of variance. The results indicated that major sources of air pollutants (PM10, PM2.5, PM1, CO, CO2) at the residential sites are road dust raised by vehicular movement, spillage of coal generated during transportation, spontaneous combustion of coal, and biomass burning in village area.  相似文献   

20.
The increasing emission of primary and gaseous precursors of secondarily formed atmospheric particulate matter due to continuing industrial development and urbanization are leading to an increased public awareness of environmental issues and human health risks in China. As part of a pilot study, 12-h integrated fine fraction particulate matter (PM2.5) filter samples were collected to chemically characterize and investigate the sources of ambient particulate matter in Guiyang City, Guizhou Province, southwestern China. Results showed that the 12-h integrated PM2.5 concentrations exhibited a daytime average of 51 ± 22 µg m?3 (mean ± standard deviation) with a range of 17–128 µg m?3 and a nighttime average of 55 ± 32 µg m?3 with a range of 4–186 µg m?3. The 24-h integrated PM2.5 concentrations varied from 15 to 157 µg m?3, with a mean value of 53 ± 25 µg m?3, which exceeded the 24-h PM2.5 standard of 35 µg m?3 set by USEPA, but was below the standard of 75 µg m?3, set by China Ministry of Environmental Protection. Energy-dispersive X-ray fluorescence spectrometry (XRF) was applied to determine PM2.5 chemical element concentrations. The order of concentrations of heavy metals in PM2.5 were iron (Fe) > zinc (Zn) > manganese (Mn) > lead (Pb) > arsenic (As) > chromium (Cr). The total concentration of 18 chemical elements was 13 ± 2 µg m?3, accounting for 25% in PM2.5, which is comparable to other major cities in China, but much higher than cities outside of China.  相似文献   

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