Spatial distribution and sources of polycyclic aromatic hydrocarbons (PAHs) in green mussels (Perna viridis) from coastal areas of Peninsular Malaysia: implications for source identification of perylene

Distribution of polycyclic aromatic hydrocarbons (PAHs) was determined in green mussels (Perna viridis) from various sites in coastal waters of Peninsular Malaysia between August 2004 and January 2007, in order to assess contamination by petroleum hydrocarbons. The range of ∑PAHs detected in mussels was from 766 to 110500 (ng/g lipid wt.). High concentrations of PAHs were found in mussel tissues collected near Penang Bridge. The ratios of methyl phenanthrenes to phenanthrene (∑MP/P ratio) for Penang, Kg. Pasir Puteh and Tebing Runtuh (Johore Straits) were greater than 2, indicating extensive input of petrogenic PAHs. The results indicated that male individuals elevated more considerable concentrations of PAHs in their soft tissues in comparison to female individuals. The results of independent sample T-test showed that there were no significant differences (p > 0.05) between male and female mussels analysed in the Pasir Panjang station. Negative significant correlations (r = ?0.890, p < 0.01) and (r = ?0.0655, p < 0.05), were found between weight and total of PAHs in female and male species, respectively. This indicated that body weight of each individual was not affected by the PAHs concentrations. The present study proposes the use of soft tissue of Perna viridis as a biomonitor of perylene bioavailability and contamination in coastal waters of Peninsular Malaysia.     

Principal component analysis application in polycyclic aromatic hydrocarbons “mussel watch” analyses for source identification

This article aims to show how a careful pre-treatment of data can be used to demonstrate various features embedded in a given data set obtained from a “mussel watch” survey, namely site- and source-specific characteristics and weather-related changes, and to provide indications so as to allow comparison with analyses performed on another substrate matrix. Polycyclic aromatic hydrocarbons (PAHs) biomonitored in the aquatic environment by means of caged mussels are compared by site and by season. Moreover, their fingerprints were compared to marine sediments and atmospheric airborne PAHs. The characterization of the sampling stations by means of the multivariate technique called principal component analysis (PCA) allows distinguishing the prevalence of pyrogenic or petrogenic types of pollution and between two kinds of combustibles. This was confirmed by jointly analyzing the percent composition of sea (mussel) and air (filter) samples.     

低功率因数电功率表在使用中应注意的问题

通过分析电功率表的测量原理、接线方式和读数方法,详细介绍低功率因数电功率表在使用中应该注意的问题。     

自制数字式光学定律演示仪

采用旋转电位器与数字表头制做了数字式光学定律演示仪，它能够演示光的反射定律，折射定律，全反射现象。     

利用智能毫秒表改进大学物理实验计时系统的尝试

在大学物理实验中,有很多实验使用人工秒表计时,由于系统误差较大往往不能得到理想的实验结果,而经过改进采用数字毫秒表计时后,就解决了这个问题,使实验误差控制在百分之一以内。     

Analysis of 32 priority substances from EU water framework directive in wastewaters,surface and drinking waters with a fast sample treatment methodology

A simple, fast, and sensitive method is proposed for the analysis of 32 priority substances (PS) from EU Water Framework Directive (WFD) and the first Watch List in effluents of wastewater treatment plants (EWW), surface waters (SW) and drinking waters (DW). Dispersive liquid-liquid microextraction (DLLME) and gas chromatography coupled to tandem mass spectrometry (GC-MS/MS) is used. For DLLME, a mixture of 1,1,2-trichloroethane as extraction solvent (75 µL) and acetonitrile as disperser solvent (3.2 mL) is proposed. The method was validated in EWW, SW and DW, showing satisfactory accuracy values ranging from 90% to 104%, good precision (relative standard deviation, RSD%, lower than 13%) and uncertainty values between 7% and 34%. Regarding sensitivity, method limits of quantification (MLOQs) of 4.8, 5.2 and 8.8 ng L^?1 for DW, SW and EWW, respectively, were obtained. The developed method was applied to analyze PS in water from effluents of waste water treatment plants (WWTPs), surface water of the Llobregat River and its main tributaries (Catalonia, NE Spain) and drinking water from a Drinking Water Treatment Plant (DWTP). Moreover, the efficiency of treatment plants (DWTP, WWTP) on the elimination of PS was evaluated. Only 3 PS (lindane, terbutryn and dicofol) were detected, being terbutryn the compound found at the highest levels (up to 493 ng L^?1 in EWW samples). Regarding environmental quality standard (WFD) for terbutryn in surface waters, only one sample, the Rubí stream (431 ng L^?1), showed levels of terbutryn higher than maximum allowable concentration (340 ng L^?1).