京杭运河上游河段磷污染时空分布特征及污染源解析

为揭示京杭运河上游桐乡段总磷浓度不能稳定达到GB 3838—2002《地表水环境质量标准》Ⅲ类标准的原因,在桐乡段干流布设24个采样点,入河支流布设18个采样点,开展水质加密监测,研究磷污染发生的时空变化规律;基于水质常规指标的主成分分析,以及各主成分因子中强载荷指标与三维荧光组分的相关性分析,对重点河段磷的主要污染源进行解析;并基于绝对主成分—多元线性回归模型,定量评价主要磷污染源的贡献率。结果表明：1）京杭运河上游桐乡段干流入境水总磷浓度为0.14~0.20 mg/L,沿程监测点5~7、9和21~24有明显变差趋势,最高浓度达0.40 mg/L;部分入河支流水质较差,总磷浓度达到0.44 mg/L。2）主成分分析得到3个主因子,因子1以氨氮、溶解态磷为主要载荷,与类蛋白质组分显著相关,代表生产生活污染;因子2以高锰酸盐指数、溶解态磷、颗粒态氮为主要载荷,与类腐殖质组分显著相关,代表农业源;因子3以颗粒态磷、颗粒态氮为主要载荷,与浊度显著相关,代表码头污染与底泥源。3）运河上游河段的磷污染主要发生在干流监测点5~7和9,主要为码头污染与底泥源,其在丰水期和平水期的贡献率分别为65.9%和31.8%;监测点21~24主要为农业源,其在丰水期和平水期的贡献率分别为34.0%和32.1%;此外,生产生活污染在丰水期也有较大影响,其对监测点5~7和9、21~24的贡献率分别为42.6%、31.8%。

     

The Effect of Grain Size and Element Concentration in Identifying Contaminant Sources

The distribution of metal contaminants between different size fractions of marine sediments is well known. However, the use of size normalization techniques may alter the ability or usefulness in identifying potential sources in complex environments. In a reassessment of metal data from the shelf area of Sydney, Australia, the mud and sand fractions were investigated separately by PCA and PLS methodologies. The analyses were able to produce clear distinctions between industrial/urban sources when based on a suite of metals rather than individual (single-element) concentrations. Signature analysis by PLS with copper, lead, zinc, manganese, chromium, cobalt, nickel, and cadmium demonstrated the dispersion of the fine-grained contaminated material to the south in the East Australian Current. However, due to the commonality between many of the metals, a subset of four metals was used to define the signature. This significantly improved separation, showing clear plumes extending ～30 km from the source rivers.     

苏州市区灰霾现象形成的气象条件分析

随着社会和经济的快速发展,灰霾现象的发生有逐渐上升趋势,严重影响城市形象和群众的身心健康。苏州市的灰霾现象发生频率1—2月最高,7—8月最低。通过寻找形成灰霾现象的主要气象控制因子,有助于判别不同气象条件在灰霾天气形成中的作用。采用基于因子分析的主成分提取方法,将6个气象因子观测资料整合为3个主成分,并逐一揭示4个典型季节各主成分的支配因子在灰霾天气形成中的作用。结果表明,热量条件是影响1—2月、4—5月和7—8月霾日形成的主要气象条件。动力条件是10—11月霾日形成的主要气象条件,水分条件影响相对较弱,仅起辅助作用。     

The Distribution and Sources of Polycyclic Aromatic Hydrocarbons in Surface Sediments Along the Egyptian Mediterranean Coast

Coastal marine sediment samples were collected from 31 sampling stations along the Egyptian Mediterranean Sea coast. All sediment samples were analyzed to determine aliphatic and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC) contents and grain size analysis. Total concentrations of 16 EPA-PAHs in the sediments were varied from 88 to 6338 ng g⁻¹ with an average value of 154 ng g⁻¹ (dry weight). However, the concentrations of total aliphatic were varied from 1.3 to 69.9 ng g⁻¹ with an average value of 15.6 ng g⁻¹ (dry weight). The highest contents of PAHs were found in the Eastern harbor (6338 ng g⁻¹), Manzala (5206 ng g⁻¹) and El-Jamil East (4895 ng g⁻¹) locations. Good correlations observed between a certain numbers of PAH concentrations allowed to identify its origin. The average total organic carbon (TOC) percent was varied from 0.91 to 4.54%. Higher concentration of total pyrolytic hydrocarbons (∑COMB) than total fossil hydrocarbons (∑PHE) declared that atmospheric fall-out is the significant source of PAHs to marine sediments of the Egyptian Mediterranean coast. The selected marked compounds, a principal component analysis (PCA) and special PAHs compound ratios (phenanthrene/anthracene vs fluoranthene/pyrene; ∑COMB/∑EPA-PAHs) suggest the pyrogenic origins, especially traffic exhausts, are the dominant sources of PAHs in most locations. Interferences of rather petrogenic and pyrolytic PAH contaminations were noticed in the harbors due to petroleum products deliveries and fuel combustion emissions from the ships staying alongside the quays.     

堆肥过程中有机质和微生物群落的动态变化

利用3个容积约为50 L的平行生物反应装置研究堆肥过程中温度、湿度（水分含量）、pH值和有机质的动态变化情况。按照Van Soest方法根据有机质不同的溶解特性将其分为：溶于沸水的有机质H2O、溶于中性试剂的有机质SOLU、半纤维素（HEMI）、纤维素（CELL）和木质素（LIGN）。结果表明：反应装置内环境湿度调控在60%左右时,堆肥系统内借助生化反应,温度最高可达到约50℃。堆肥材料在反应初期呈现偏酸性（pH=6.5）,而随着反应的发生,pH逐渐变为中性或弱碱性（pH=7.4）。经过20 d的堆肥实验,有机质总量降解了约47%。在微生物作用下的各类有机质的降解率不同,按大小排序为H2O〉HEMI〉CELL〉SOLU〉LIGN,其降解率分别是85%、56%、36%、32%和27%。为了深入理解堆肥过程中有机质的降解机制,文章采用磷脂脂肪酸（PLFAs）技术对体系中的微生物群落变化进行了初步分析,发现微生物优势群落随反应温度的改变发生明显变化,在堆肥初期和堆肥中期,细菌占优势,而堆肥末期时真菌比例较高。在堆肥的过程中,革兰氏阴性菌的比例呈下降趋势,而革兰氏阳性菌的比例呈上升趋势。     

Comparative Metal Distribution in Hair of Pakistani and Libyan Population and Source Identification by Multivariate Analysis

Using nitric acid-perchloric acid wet digestion based FAAS method ten selected metals (Cd, Co, Cr, Fe, K, Mn, Na, Ni, Pb and Zn) were determined in the scalp hair of male Pakistani and Libyan donors (n = 62), between 3–54 years age and residing in typical urban areas. The study was taken up to identify sources of metal distribution in two diverse population segments exposed to different environments. Sodium emerged with the highest mean hair concentration of 511.0 μg/g and 496.9 μg/g for Libyan and Pakistani donors respectively, followed by K, at 266.2 μg/g and 242.4 μg/g for the two donor categories. Cadmium showed the lowest mean hair concentration for both Pakistani (0.380 μg/g) and Libyan (0.530 μg/g) donors. Levels of Na, K, Pb, Cr and Cd were higher in hair of Libyan donors compared with Pakistani counterparts which showed higher comparative levels of Zn, Fe, Co, Ni and Mn. Strong metal-to-metal correlations were found between Na–K (r = 0.638) and Cd–Co (r = 0.574) for Pakistani donors, while for Libyan donors, Na–K (r = 0.680) and Fe–Mn (r = 0.624) correlations emerged as strongly significant. Only K was found to have a strong positive correlation (r = 0.611) with age for Pakistani donors while this correlation was significantly negative (r = −0.500) for Libyan donors, probably arising from individual food habits. Other metals showed no viable relationship with age. Principal Component Analysis (PCA) and Cluster Analysis (CA) of the data evidenced food, industrial emissions and automobile emissions as possible sources of metal distribution. The results of the present study are compared with those reported for subjects from other regions of the world.     

Does Soil Acidification Affect Spruce Needle Chemical Composition and Tree Growth?

In 1994, a large survey of soil chemistry was undertaken in thecounty of Värmland in central Sweden (Lundström et al., 1998).The southern part of the county was affected by soilacidification whereas there were no such indications in thenorthern part. To investigate the influence of soil chemistryon the trees at the specific sites, the survey was continued byan analysis of needle chemistry (Norway spruce) which wasundertaken at 150 of the 180 sites, and of tree growth at 65 ofthe 180 sites. Growth was expressed as a ratio between expectedgrowth, estimated with a national, empirical growth model, andthe growth observed in the field. In statistical analyses,using rank correlation, PCA and PLS, there were only weakindications of an influence of soil chemistry on needlechemistry and on tree growth. A moderate correlation betweennitrogen and sulphur in needles was found, which wasinterpreted as an effect of deposition and of processes in thetree canopy. No obvious regional pattern of the growth ratiowas found, in contrast to the clear pattern of soilacidification. The statistical analysis could not with anycertainty point out any of the soil chemistry variables asespecially important for the tree growth ratio.     

Continuous performance assessment and improvement of integrated HSE and maintenance systems by multivariate analysis in gas transmission units

In this study, an integrated “Health, Safety, and Environment (HSE)” and maintenance systems are presented. Multivariate analysis is used for continuous performance assessment and improvement of these systems. The two subjects of “Maintenance System” and “HSE” have been individually investigated several times in different studies. However, few studies have been done to integrate these two systems and provide an integrated system for their implementation. This study evaluates current maintenance and HSE systems of a Gas Transmission Unit by Data Envelopment Analysis (DEA) and Principal Component Analysis (PCA). Moreover, decision making units (DMUs) are examined and ranked. Employees are considered as DMUs. This is done through investigating and measuring their efficiencies and identifying the inefficient and less-efficient units. Since an increase in the number of inputs does not lead to an increase in the number of outputs with the same scale, an output-oriented DEA with a Variable Returns to Scale (VRS) is used. The Fuzzy DEA (FDEA) is also used in this research to decrease uncertainty existing in qualitative indicators and human error. Finally, suggestions are given to improve those DMUs. The managers and employees of the gas transmission unit constitute the statistical population of the study. To achieve the objectives of this study, standard questionnaires with respect to HSE and Maintenance system are completed by operators. The proposed approach would help policy makers and top managers of Gas Transmission Company to have a more comprehensive and thorough understanding the working conditions with respect to the maintenance and HSE features.     

基于实测光谱与MODIS数据的太湖悬浮物定量估测

以太湖为研究区域,对太湖水体的水面反射光谱进行实地测试,并取样在实验室进行水质分析;根据光谱分析得到的悬浮物特征波段,估测悬浮物浓度;最后,对比MODIS波段,用最敏感波段及主成分分析法建立悬浮物估测模型.结果表明,576nm附近的反射率峰值、841nm处反射率一阶微分值和808nm附近的反射峰高与悬浮物浓度都有较好的相关性,其中峰高法和一阶微分法对悬浮物浓度的估测精度相当;MODIS波段1与悬浮物浓度相关性最好,经过主成分变化后的第一主成分和第二主成分可以较好地估测悬浮物浓度.因此,可利用MODIS数据对太湖悬浮物进行长期动态监测.     

Use of thermal desorption-gas chromatography-mass spectrometry (TD-GC-MS) on identification of odorant emission focus by volatile organic compounds characterisation

Volatile organic compounds (VOCs) from several different municipal solid wastes’ treatment plants in Mallorca (Spain) have been analysed by thermal desorption-gas chromatography-mass spectrometry (TD-GC-MS). Ambient (immission) air was collected during February and March 2011 by active sampling onto sorbents Tenax™ TA and Carboxen™ 1000. The study presents the chemical characterisation of 93 volatile organic compounds (VOCs) from an overall set of 84 immission air samples. 70 VOCs were positively identified.The linear fit for all 93 external standard calibration, from 10 mg L⁻¹ to 150 mg L⁻¹ (n = 4), was within the range 0.974 < r² < 0.998. Limits of detection of the method (LOD) for all the standards were within the range 1.1-4,213 pg, as the absolute standard amount spiked into sorbent tubes in 1 μL standard mixture (dissolved in methanol).Overall results stated systematic correlation between waste’s nature and VOCs’ air composition. Organic wastes show main contribution of terpenes, waste water sludge residues’ of reduced sulphured compounds (RSCs) and municipal solid wastes show contribution of a wide sort of VOCs. The use of a chemometric approach for variable’s reduction to 12 principal components enables evaluation of similarities and dissimilarities between facilities. PCA clearly related samples to its corresponding facility on the basis of their VOCs composition and the ambient temperature.