The Chemistry of Soils, Rocks and Plant Bioindicators in Three Ecosystems of the Holy Cross Mountains, Poland

In June of 2000, biogeochemical study was carried out in three ecosystems of the Holy Cross Mountains (south-central Poland). This paper presents element concentrations and stable sulfur (and in one site lead) isotope ratios in rocks, detailed soil profiles, and plant bioindicators including epiphytic lichen Hypogymnia physodes (L.) Nyl., mosses (Pleurozium schreberi (Brid.) Mitt., Hypnum cupressiforme Hedw. S. Str., Hylocomium splendens (Hedw.) B.S.G.), Scots pine (Pinus sylvestris L.), common birch (Betula pendula Roth.), aspen (Populus tremula L.) and English oak (Quercus robur L.). Chemical analyses were performed with ICP-AES and AAS methods in the accredited laboratory (Central Chemical Laboratory of the Polish Geological Institute in Warsaw). The principal objective of this study was to compare the chemical composition of rocks, soils and selected plant bioindicators between investigation sites using the same methods of sample collection, preparation and analyses. The results of this study have shown that there is a high variability in concentrations of elements in plant bioindicators from the same sites that can not be explained only by soil properties or anthropogenic influence. This conclusion indicates that for biomonitoring purposes (especially with vascular plants) we cannot neglect individual features of the species examined.     

Connecting sources, fractions and algal availability of sediment phosphorus in shallow lakes: An approach to the criteria for sediment phosphorus concentrations

Although point and nonpoint sources contribute roughly equal nutrient loads to lakes, their relative role in supporting algae growth has not been clarified. In this research, we have established a quantitative relationship between algae-available phosphorus (P) and P chemical fractions in sediments; the latter indicates the relative contribution of point versus nonpoint sources. Surface sediments from three large shallow lakes in eastern China, namely, the Chaohu, Taihu and Hongzehu Lakes, were sampled to assess their algae-available P and chemically extracted P fractions. The algae-available P primarily comes from iron/aluminium (hydr)oxide-bound P (Fe/Al-bound P), 45% of which is algae-available P. The ratio of Fe/Al-bound P to calcium compound-bound P (Ca-bound P) indicated the relative contribution of point to nonpoint sources, with the point sources contributing the majority of increased Fe/Al-bound P in sediments. Therefore, the reduction of point sources from urbanized areas, rather than nonpoint sources from agricultural areas that primarily contribute to the Ca-bound P fraction, should be prioritized to alleviate cyanobacterial algal blooms (CyanoHABs) in shallow lakes with sediment P as a potential source to support algae growth. With these important results, we proposed a conceptual model for “P-pumping suction” from sediments to algae to aid in the development of the criteria for sediment P concentrations in shallow lakes.     

Toxicity assessing for chlorpyrifos-contaminated soil with three different earthworm test methods

Earthworm toxicity tests are useful tools for terrestrial risk assessment but require a hierarchy of test designs that differ in effect levels (behavior, sublethal, lethal). In this study, the toxicity of chlorpyrifos contaminated soil on earthworms was assessed. In addition to the acute and chronic tests, an avoidance response test was applied. Earthworms were exposed to sublethal and lethal concentration of chlorpyrifos, and evaluated for acute toxicity, growth, fecundity and avoidance response after a certain exposure period. The test methods covered all important ecological relevant endpoints (acute, chronic, behavioral). Concentration of 78.91 mg/kg, chlorpyrifos caused significant toxic effects in all test methods, but at lower test concentrations, only significant chronic toxic effects could be observed. In the present study, chlorpyrifos had adverse effect on growth and fecundity in earthworm exposed to 5 mg/kg chlorpyrifos after eight weeks. The avoidance response test, however, showed significant repellent effects concentration of 40 mg/kg chlorpyrifos. For chlorpyrifos, concentration affecting avoidance response was far greater than growth and fecundity, it seemed likely that earthworms were not able to escape from pesticide-contaminated soil into the clean soil in field and hence were exposed continuously to elevated concentrations of pesticides.     

区域风险评价方法研究

基于定量风险评价的基本原理,提出一种区域风险评价方法。主要针对有多个重大危险源存在的区域,在对单个危险源进行风险评价的基础上,应用叠加原理得到描述该区域整体风险状况的定量评价结果。同时考虑了消防部门和医疗机构在事故应急救援中的积极作用,并将其量化为区域风险的补偿系数。通过实例验证了该方法的可行性,展示了该方法的应用效果。区域风险评价方法不仅能够反映区域风险的分布状况,而且对区域重大危险源的规划和布局具有较好的决策支持作用。     

基于地面监测数据的2013~2015年长三角地区PM2.5时空特征

近年来,长三角地区灰霾天气持续增多,空气细颗粒物污染问题日益突出。基于2013年1月至2015年5月长三角地区及周边缓冲区内共214个空气质量监测站点PM_2.5逐时监测数据,运用普通克里金插值方法,从年、季、月尺度上分析了PM_2.5的空间分布格局和时间动态变化。结果表明:(1)2 a来,长三角地区PM_2.5浓度空间分布明显呈现整体北部高南部低,局部地区略有突出的分布特征;长三角地区PM_2.5浓度年均值为57.08μg/m³;其中,江苏省PM_2.5的年均值为三省市最高,为65.84μg/m³;其次为上海市,年均值为53.87μg/m³;浙江省PM_2.5的年均值较小,为51.53μg/m³。(2)从季节尺度分析,长三角地区PM_2.5浓度变化表现出冬春季高,夏秋季低的变化趋势;这与区域内冬季风向来源、降水稀少、气象扩散条件差有着密切的关系; (3)长三角地区月浓度变化大致呈U形分布; 12月份PM_2.5浓度最高; 3月份以后, PM_2.5浓度开始呈逐步下降趋势;在5~9月份,区域PM_2.5处于"U"字的谷底,其中6月份夏收时期秸秆焚烧、气象等因素导致PM_2.5浓度有略微升高;进入10月份后迅速攀升,且11、12月份呈现持续升高态势。     

杭州市家庭室内空气中PBDEs的污染现状与特征

分析评价了杭州市家庭室内空气中多溴联苯醚(PBDEs)的污染现状及特征.结果显示:杭州家庭客厅空气中气相和颗粒相PBDEs的总浓度平均值分别为52.57 pg·m-3,范围为21.37～83.47 pg·m-3、卧室浓度为43.78 pg·m-3,范围为28.72～58.75 pg·m-3,BDE-47和BDE-99是家庭室内空气中最重要的两种单体,占总浓度的62.75％.室内空气中气相PBDEs浓度是颗粒相的1.49倍.高层建筑中的PBDEs浓度与低层建筑差别不大,均处于较低水平.PBDEs的理化性质、环境条件是影响其气固分配的重要因素.     

快速消解分光光度法测定低浓度水样化学需氧量的不确定度评定

摘要：运用测量不确定度评定的方法和程序,分析了快速消解分光光度法（HJ／T399—2007）测量水质化学需氧量测试过程中不确定度的来源,主要是标准溶液配制、标准曲线拟合、样品重复测定、分光光度计、取水样体积这五部分引入的不确定度。本次测量相对合成不确定度为0．027;最大的相对不确定度分量是标准曲线拟合引起的,相对不确定度为0．015;最小的相对不确定度分量是取水样体积引起的,相对不确定度为0．0032;本次测量结果为：56．0mg／L±3．04mg／L,k=2。     

Leaching of styrene and other aromatic compounds in drinking water from PS bottles

Bottled water may not be safer, or healthier, than tap water. The present studies have proved that styrene and some other aromatic compounds leach continuously from polystyrene （PS） bottles used locally for packaging. Water sapmles in contact with PS were extracted by a preconcentration technique called as ＂purge and trap＂ and analysed by gas chromatograph-mass spectrometer （GC/MS）. Eleven aromatic compounds were identified in these studies. Maximum concentration of styrene in PS bottles was 29.5 μg/L. Apart from styrene, ethyl benzene, toluene and benzene were also quantified but their concentrations were much less than WHO guide line values. All other compounds were in traces. Quality of plastic and storage time were the major factor in leaching of styrene. Concentration of styrene was increased to 69.53 μg/L after one-year storage. In Styrofoam and PS cups studies, hot water was found to be contaminated with styrene and other aromatic compounds. It was observed that temperature played a major role in the leaching of styrene monomer from Styrofoam cups. Paper cups were found to be safe for hot drinks.     

Impacts of converting from leaded to unleaded gasoline on ambient lead concentrations in Jakarta metropolitan area

Total suspended particulate mater （TSP） concentrations were monitored for one year from July 2000 and for one year from April 2003 in Jakarta City. Thirteen elemental TSP components, aluminum （Al）, sodium （Na）, iron （Fe）, lead （Pb）, potassium （K）, zinc （Zn）, titanium （Ti）, manganese （Mn）, bromine （Br）, copper （Cu）, chromium （Cr）, nickel （Ni）, and vanadium （V） were analyzed by a sequential X-ray fluorescence spectrometer. Al, Na, Fe, K, and Pb were major components at most of the sampling locations in 2000. However, only Pb in 2003 dramatically decreased to one tenth. The phase-out of leaded gasoline began on July 1, 2001 in Jakarta City and lead content in gasoline decreased to one tenth, too. The decrease in Pb concentration was a result of the phase-out of leaded gasoline, as lead emissions mainly are exhaust gas from vehicles.     

火焰原子吸收光谱法测定电镀废水中高浓度的锡

采用盐酸消解样品,用火焰原子吸收光谱法测定电镀废水中高浓度的锡的质量浓度,方法简单可靠。通过实验样品的分析,验证了方法的准确度和精密度。该方法干扰少,数据准确,适合废水分析。