兰州市取暖期可吸入颗粒物中单颗粒矿物组成特征

为研究兰州市2005年冬季大气可吸入颗粒物(PM10)中单颗粒的矿物组成,用能谱扫描电镜识别和统计了兰州市区(东方红广场)和郊区(榆中县)两个采样点的单矿物颗粒。结果在市区样品中识别出方解石、伊/蒙混层、石英、斜长石、伊利石、石膏、绿泥石、高岭石、浊沸石和钾长石等21种矿物,前7种占统计总量的75%以上;郊区样品中识别出20种矿物,以方解石、石英、伊利石、绿泥石、斜长石和伊/蒙混层为主(占70%以上),与市区相比缺少钾石膏、金红石和水铝酸钙而增加了硫酸镁和磷灰石。总体来看,大气PM10中的矿物颗粒可分为粘土类、长石类、碳酸盐类、硫酸盐类、氧化物类和其他六类,以粘土类和碳酸盐类矿物为主(约占60%);冬季市区颗粒物表面的“硫化”现象较郊区严重;这些矿物颗粒主要来自地表土,人为排放和大气中二次化学反应生成的矿物的贡献较小。     

Size Distributions and Elemental Compositions of Particulate Matter on Clear, Hazy and Foggy days in Beijing, China

Total suspended particulates(TSP)samples were collected using low pressure impactors(Andersen Series 20-800,USA)on typical clear,hazy and foggy days in Beijing in order to investigate the characteristics of size distributions and elemental compositions of particulate matter(PM)in different weather conditions. The concentrations of sixteen elements,including Na,Mg,Al,K,Ca,Mn,Fe,Ni,Cu,Zn,As,Se,Cd,Ba,Tl and Pb were detected using inductively coupled plasma mass spectrometry(ICP-MS).The results showed that Ca,Al,Fe,Mg and Ba on foggy days were 2.0-2.6 times higher than on clear days,and 2.3-2.9 times higher than on hazy days.Concentrations of Cu,Zn,As,Se and Pb on foggy days were 163.5,1186.7,65.9,32.0 and 708.2 ng m-3,respectively,in fine particles,and 68.1,289.5,19.8,1.6 and 103.8 ng m-3,respectively,in coarse particles.This was 1.0-8.4 times higher and 1.4-7.4 times higher than on clear and hazy days,respectively.It is then shown that Mg,Al,Fe,Ca and Ba were mainly associated with coarse particles,peaking at 4.7-5.8μm;that Cd,Se,Zn,As,Tl and Pb were most dominant in fine particles,peaking at 0.43-1.1μm;and that Na,K,Ni,Cu and Mn had a multi-mode distribution,with peaks at 0.43-1.1μm and 4.7-5.8μm.The enrichment factors indicated that coal combustion along with vehicle and industry emissions may be the main sources of pollution elements.     

三峡小江回水区透明度季节变化及其影响因子分析

三峡成库后其季节调蓄过程使该水域湖沼学特征具有独特性.根据三峡小江流域回水区段为期2年的定位跟踪观测,对透明度(SD)和主要环境指标的相互关系进行分析研究.研究期间,小江回水区透明度均值为170±7cm,各采样点透明度差异不明显且季节变化过程一致,自春末夏初开始降至最低水平,夏季汛期相对稳定,夏末入秋持续升高,冬季维持在较高状态,入春后下降.对透明度和主要环境指标的相关性分析发现,无机悬浮颗粒(PIM)是影响透明度的主要指标.透明度同PIM、Chl.a多元回归模型为:SD=(-89.389±8.101)·lg(PIM)+(-84.008±8.624)·lg(Chl.a)+(264.132±8.232).汛期低水位状态下(145-150m)小江回水区水动力条件趋于天然河道,河道输沙量增加使无机悬浮颗粒含量远高于藻类生物量而成为影响透明度的主要环境指标.在中水位(150-156m)和高水位(156m以上),虽然藻类进入非生长季节,但水位抬升和水体滞留时间的延长促使悬浮颗粒物大量沉淀,悬浮生长于表层水体的藻类成为影响透明度的主要环境指标,生物作用对透明度的影响明显.     

中国东部主要河流稀土元素地球化学特征

在2007年底至2008年初的枯水期间,系统采集了中国东部流域面积和径流量较大的33条河流沉积物、悬浮颗粒物和水样,采用等离子质谱法、X荧光光谱法等方法测定了14种稀土元素含量以及常量组分和水体pH值等理化指标。研究发现中国河流稀土元素浓度总体高于世界均值,且南方河流沉积物、悬浮物稀土元素含量高于北方河流,南方河流悬浮物态中稀土、重稀土呈现一定程度的相对富集,与我国上地壳稀土丰度和稀土矿产种类的南北分异相吻合。展示了以中国东部泥质岩稀土元素丰度标准化后的稀土配分模式及Ce、Eu异常特征,发现河流沉积物的中、重稀土元素相对富集,悬浮物轻稀土相对富集,溶解相重稀土富集的特征;北方河流溶解相稀土元素浓度明显大于南方河流,且除小清河外,溶解相Eu不同于沉积物与悬浮物而呈强烈的正异常,主要与河水理化性质影响下的稀土分异有关。研究发现小清河等少数河流沉积物中稀土元素为异常高值,经Al标准化处理、计算拟合剩余值后,认为小清河等河流稀土元素已受人为污染的影响。     

河水中悬浮颗粒物对重金属的吸附行为

本研究以瓯江河水为对象,研究河水中悬浮颗粒物对重金属（Cu、Zn、Cd、Pb）离子的吸附行为．分别进行了Cu、Zn、Cd、Pb在悬浮颗粒物的吸附速率,解吸速率以及溶解性有机质（DOM）对吸附解吸行为的影响实验．结果表明：河水中悬浮颗粒物对Cu、Zn、Cd、Ph的吸附和解吸速率较快,吸附平衡时间为8h,解吸平衡时间为4h...     

阿塔卡马海沟表层水颗粒有机碳与微生物群落呼吸作用的时空变化研究

海沟是全球大洋体系的重要组成部分。研究这一极端环境的生物地球化学循环过程有助于我们进一步理解海洋的物质循环。前期研究发现,海沟表层水体的初级生产力(NPP)对海沟沉积物埋藏的有机碳性质具有重要影响,但是,颗粒有机碳(POC)在沉降过程中被微生物呼吸和降解的过程尚不清楚。因此,本研究利用2018年春"太阳号"阿塔卡马海沟(Atacama Trench)国际联合航次SO261所采集的表层水样品,测试其中POC浓度、C/N、δ¹³C、δ¹⁵N等参数,并结合0.2—0.8、0.8—3.0、>3.0μm三种粒径微生物群落呼吸(microbial community respiration,MCR)速率测试,探究其日变化模式及不同站位的空间变化模式,进而衡量微生物对POC的呼吸降解作用。结果表明,该海域表层水中对POC降解占主导作用的微生物类群粒径为0.8—3.0μm;24 h时间序列实验表明MCR随时间呈现"M"型曲线的双峰变化模式,且和C/N、δ¹³C、δ¹⁵N等参数变化趋势吻合,表明同一站位的呼吸速...     

安徽省大气颗粒物污染特征分析

对2016年全年颗粒物监测浓度数据进行统计分析,得到了安徽省颗粒物污染的空间分布、浓度和粒径,以及污染传输特征。结果表明,淮河以北、沿江和江淮之间、长江以南和皖南山区城市颗粒物污染随地理位置不同表现出明显的区域化特征,污染程度由北向南减轻,污染过程明显表现出由北向南逐步扩散传输的规律,污染程度越重,污染深入南方的范围越广,持续时间也越长。冬季污染较重的城市,上午出现明显的高浓度时段,全天变化为"双峰双谷"型。夏、秋季节夜间细颗粒物(PM_2.5)浓度贡献比增加。PM_2.5与PM₁₀(可吸入颗粒物)质量浓度比值冬季最高,春季较低。污染重的城市冬季PM_2.5占比高。     

胶州湾海水中悬浮颗粒对溶解态微量元素的影响

运用离子色谱离线螯合结合ICP-MS的方法,对胶州湾海水中的微量元素(V,Co,Ni,Cu,Mo,Cd,Pb,U,REEs)进行了精确的定量分析。在测试前对在同一站位不同层位采集的平行海水样品进行了两种不同的酸化处理:一份采取先过滤后酸化的方式,以获得海水中溶解态微量元素的含量;另一份采取直接酸化后分析的方式,以评估悬浮颗粒中的可交换态微量元素对溶解态微量元素测定结果可能造成的影响。通过对比研究发现,不同处理方法得到的V、Ni、Cu、Co、Pb以及稀土元素(REEs)的质量浓度存在很大差异,说明悬浮颗粒物质可能对海水中相应元素的测定产生较大的影响。各种微量元素之间的差异和相应离子或离子团的电荷性质、在海水中的配位作用以及悬浮颗粒物质的表面电荷性质有关。初步研究结果表明,在类似于胶州湾这样的近海海域,悬浮颗粒物质是控制微量元素分布特征的一个重要因素。     

A comparative study of mercury contamination in the Tagus estuary (Portugal) and major French estuaries (Gironde,Loire, Rhône)

Concentrations of mercury were determined for the waters, suspended matter and sediments of the Tagus and of major French estuaries.The Tagus estuary is one of the most contaminated by mercury derived from the outfalls of a chloralkali plant and from other industrial sources. In deposited sediments the median level, 1·0 μg Hg g^?1, is twenty times higher than the natural background and Hg contents depend on the sediment grain-size, age and the distance from waste-outfalls. Suspended matter is more regularly and highly contaminated (median value: 4·5 μg Hg g^?1). In the French estuaries Hg levels in the suspended material decrease with salinity due to dilution and/or remobilization processes. In June 1982, in the Loire estuary, high values of Hg are observed in the middle estuary and attributed to urban and industrial sources.In the Tagus estuary, the general distribution of total dissolved Hg confirms the contamination: it increases seaward from 10 ng 1^?1 in the river to 80 ng 1^?1 in the estuary outlet. The dissolved Hg is almost totally organic in the river, inorganic in the middle estuary due to inorganic Hg effluents and again organic in the lower estuary. This variation is related to the dissolved organic carbon values. The dissolved Hg levels in the Loire Estuary (5–300 ng 1^?1) are much higher than in the Gironde estuary (3–6 ng 1^?1) and of the same order as those observed in the Tagus estuary.     

Particulate matter exchange across a Rjord sill

Recent studies have indicated the existence of a considerably higher planktonic biomass in the deep waters of the Saguenay Fjord as compared to corresponding depths in the adjacent St Lawrence Estuary on the other side of a shallow sill. The hypothesis that has been put forward to explain this phenomenon is related to the advection of near surface estuarine waters, at times very rich in particulate matter, over the entrance sill into the deeper waters of the fjord. Mixing processes associated with the development of a density flow, the presence of a hydraulic jump or other mechanisms are assumed to be responsible for the common occurrence of lower density subsurface water within the basin as compared to that penetrating over the sill.The exchange processes between the estuary and the fjord are described and an estimate made of the estuarine water volume that penetrates into the lower layer of the fjord over a semidiurnal tide cycle. From these calculations, the replacement time for the outer basin was estimated to range between one and four days. The biological characteristics of this water were used to establish a budget for particulate matter exchange which showed, in early August, a typical net input of ? 188 t of particulate organic carbon into the deep waters of the fjord over one tide cycle.