Field application of SPME as a novel tool for occupational exposure assessment with inhalational anesthetics

Occupational exposure to inhalational anesthetics occurs routinely in operating rooms. It could induce serious health hazards and diseases. This exposure assessment is a crucial step in determining risks. In this study, a pen-shaped holder for solid-phase microextraction (SPME) sampler was successfully applied as a time-weighted average sampling tool for workshift exposure assessment of operation room staff to halothane. It proved to be very convenient for use in occupational environments such as operation rooms. Samples were analyzed by a gas chromatography-mass spectrometry. The validity of the SPME method was checked in real-world conditions with Occupational Safety and Health Administration (OSHA) 103 standard method for the determination of inhalational anesthetics. A good agreement between OSHA 103 and SPME methods was obtained and results demonstrated no statistically significant differences in anesthetic concentrations determined by the two analytical methods (p?≥?0.05). It is concluded that SPME in retracted mode could successfully be applied in occupational exposure assessment purposes.     

Radiation exposure to Marine biota around the Fukushima Daiichi NPP

The dose rates for six marine organisms, pelagic fish, benthic fish, mollusks, crustaceans, macroalgae, and polychaete worms, representative in marine ecosystems, have been predicted by the equilibrium model with the measured seawater activity concentrations at three locations around the Fukushima Daiich nuclear power plant after the accident on March 11, 2011. Model prediction showed that total dose rates for the biota in the costal sea reached 4.8E4 μGy/d for pelagic fish, 3.6E6 μGy/d for crustaceans, 3.8E6 μGy/d for benthic fish, 5.2E6 μGy/d for macroalgae, 6.6E6 μGy/d for mollusks, and 8.0E6 μGy/d for polychaete worms. The predicted total dose rates remained above the UNSCEAR’s (United Nations Scientific Committee on the Effect of Atomic Radiation) benchmark level (1.0E4 μGy/d for an individual aquatic organism), for only the initial short period, which seems to be insufficiently long to bring about any detrimental effect on the marine biota at the population level. Furthermore, the total dose rates for benthic fish and crustaceans approximated using the measured activity concentration of the biota and bottom sediment was well below the benchmark level. From these results, it may be concluded that the impact of the ionizing radiation on the marine biota around the Fukushima NPP as a consequence of the accident would be insignificant.     

Aliphatic and polycyclic aromatic hydrocarbons in the surface sediments of the Mediterranean: assessment and source recognition of petroleum hydrocarbons

Coastal marine sediment samples were collected from ten sampling stations along the Egyptian Mediterranean coast in April 2010. All sediment samples were analyzed for aliphatic (C7 to C34) and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC) contents and grain size analysis. Total aliphatic hydrocarbons ranged from 1621.82 to 9069.99 ng/g (dry weight), while aromatic hydrocarbons (16 PAHs) varied between 208.69 and 1020.02 ng/g with an average of 530.68?±?225.86 ng/g?dwt. Good correlations observed between certain PAH concentrations allowed to identify its origin. The average TOC percent was varied from 0.13 to 1.46 %. Principal component analysis was used to determine the sources of hydrocarbon pollutants in sediments of Mediterranean. Additionally, special PAHs compound ratios suggest the petrogenic origins.     

Quantitative analyses of selected polychlorinated biphenyl (PCB) congeners in water,soil, and sediment during winter and spring seasons from Msunduzi River,South Africa

The lack of information and the need for knowledge on the organic pollutants within the area of KwaZulu-Natal together with the global problem of water supply have prompted our investigation into the analyses of eight polychlorinated biphenyl (PCB) congeners in the Msunduzi River of KwaZulu-Natal, South Africa. Soil, sediment, and water samples were collected at ten different sites along the river during winter and spring seasons. Soil and sediment samples were extracted using ultra sonication with dichloromethane while water samples were liquid-liquid extracted using dichloromethane. All sample extracts were cleaned-up using a multi-layer silica gel column and analyzed with gas chromatography-mass spectrometry. Quality assurance measures were also determined. The percentage recoveries for water were 53–128 for all the PCBs analyzed, while sediment recoveries ranged between 69 and 105%. The highest total concentrations of the PCBs in sediment were 214.21–610.45 ng/g dw at the Du Toit sampling site and 30.86–444.43 ng/g dw basis at the wastewater treatment inlet for winter and spring, respectively. Soil PCB concentrations were 76.53–397.75 ng/g dw at the Msunduzi Town sampling site and 20.84–443.49 ng/g (dry weight) at the Du Toit sampling site for winter and spring, respectively. In addition, high PCB concentrations were found in effluent of the wastewater treatment inlet compared to other sampling sites, which ranged between 0.68–22.37 and 2.53–35.69 ng/mL for winter and spring seasons, respectively. In all the sampling sites selected for this study, Du Toit afforded the highest PCB concentration levels and the lowest was after chlorination at the Darvill wastewater treatment plant. The results presented are new and it is the first study of organic pollutants such as PCBs that has been carried out on this river.     

Differences in the treatment efficiency of a cold-resistant floating bed plant receiving two types of low-pollution wastewater

A floating bed system vegetated with Oenanthe javanica was adopted in this study to treat two types of low-pollution wastewater (LPW): polluted river water (PRW) and treated domestic wastewater (DW). The water was treated for 111 days during the low-temperature season. The results indicated that the total nitrogen (TN) removal rates were higher in the DW groups than in the PRW groups during the initial 30 days. This difference may stem from the different C/N ratio of the influent. As the water temperature rose above 15.5 °C after March 12, the purification capability of nitrogen in the DW groups was enhanced, and the removal rates of TN were 89.8 and 76.8 % in DW and the control 2 at 111 days. Conversely, the performance of total phosphorus (TP) removal was robust during the initial stage of the experiment, despite receiving domestic wastewater with a relatively high N/P ratio (16:1). The TP removal rates in DW were as high as 91.5 % compared to 78.9 % in PRW at 30 days. At the same time, the N/P ratios of plant tissue were higher in the DW groups compared to that in the PRW groups. Plant uptake played a significant role in nutrient removal in the PRW groups (52.5 % for TN, 68.2 % for TP), followed by sedimentation. In contrast, plant uptake only accounted for 25.3 % of TN removal and 24.1 % of TP removal in DW. The results provide engineering parameters for the future design of an ecological remediation technology for LPW purification.     

Large-scale carbon stock assessment of woody vegetation in tropical dry deciduous forest of Sathanur reserve forest,Eastern Ghats,India

Tropical dry forests are one of the most widely distributed ecosystems in tropics, which remain neglected in research, especially in the Eastern Ghats. Therefore, the present study was aimed to quantify the carbon storage in woody vegetation (trees and lianas) on large scale (30, 1 ha plots) in the dry deciduous forest of Sathanur reserve forest of Eastern Ghats. Biomass of adult (≥10 cm DBH) trees was estimated by species-specific allometric equations using diameter and wood density of species whereas in juvenile tree population and lianas, their respective general allometric equations were used to estimate the biomass. The fractional value 0.4453 was used to convert dry biomass into carbon in woody vegetation of tropical dry forest. The mean aboveground biomass value of juvenile tree population was 1.86 Mg/ha. The aboveground biomass of adult trees ranged from 64.81 to 624.96 Mg/ha with a mean of 245.90 Mg/ha. The mean aboveground biomass value of lianas was 7.98 Mg/ha. The total biomass of woody vegetation (adult trees + juvenile population of trees + lianas) ranged from 85.02 to 723.46 Mg/ha, with a mean value of 295.04 Mg/ha. Total carbon accumulated in woody vegetation in tropical dry deciduous forest ranged from 37.86 to 322.16 Mg/ha with a mean value of 131.38 Mg/ha. Adult trees accumulated 94.81% of woody biomass carbon followed by lianas (3.99%) and juvenile population of trees (1.20%). Albizia amara has the greatest biomass and carbon stock (58.31%) among trees except for two plots (24 and 25) where Chloroxylon swietenia contributed more to biomass and carbon stock. Similarly, Albizia amara (52.4%) showed greater carbon storage in juvenile population of trees followed by Chloroxylon swietenia (21.9%). Pterolobium hexapetalum (38.86%) showed a greater accumulation of carbon in liana species followed by Combretum albidum (33.04%). Even though, all the study plots are located within 10 km radius, they show a significant spatial variation among them in terms of biomass and carbon stocks which could be attributed to variation in anthropogenic pressures among the plots as well as to changes in tree density across landscapes. Total basal area of woody vegetation showed a significant positive (R ² = 0.978; P = 0.000) relationship with carbon storage while juvenile tree basal area showed the negative relationship (R ² = 0.4804; P = 0.000) with woody carbon storage. The present study generates a large-scale baseline data of dry deciduous forest carbon stock, which would facilitate carbon stock assessment at a national level as well as to understand its contribution on a global scale.     

Biomonitoring of arsenic through mangrove oyster (Crassostrea corteziensis Hertlein, 1951) from coastal lagoons (SE Gulf of California): occurrence of arsenobetaine and other arseno-compounds

In this study, we examined the bioavailability of arsenic through the mangrove oyster Crassostrea corteziensis sampled from seven coastal lagoons in SE Gulf of California during the rainy and dry seasons. As concentrations in soft tissue of oysters C. corteziensis fluctuated between 5.2 and 11.6 μg/g on dry weight; organisms from the control site presented the lowest As concentrations in the two sampling seasons. As speciation was evaluated in selected samples and indicated that arsenobetaine was the major arseno-compound accounting for 53.5–74.7 % of total As. Lower percentage contributions were obtained for nonextractable As (9.7–25.5 %) and other molecules such as arsenocholine and methyl-arsonate (<5 %). Inorganic As was detectable in only two samples, at concentrations lower than 0.1 μg/g. These As data are the first generated in NW Mexico and indicate that C. corteziensis is safe for human consumption in terms of arseno-compounds. It is evident that As bioavailability in these lagoons is low.     

Profiles,sources, and transport of polycyclic aromatic hydrocarbons in soils affected by electronic waste recycling in Longtang,south China

We studied the profiles, possible sources, and transport of polycyclic aromatic hydrocarbons (PAHs) in soils from the Longtang area, which is an electronic waste (e-waste) recycling center in south China. The sum of 16 PAH concentrations ranged from 25 to 4,300 ng/g (dry weight basis) in the following order: pond sediment sites (77 ng/g), vegetable fields (129 ng/g), paddy fields (180 ng/g), wastelands (258 ng/g), dismantling sites (678 ng/g), and former open burning sites (2,340 ng/g). Naphthalene, phenanthrene, fluoranthene, pyrene, chrysene, and benzo[b]fluoranthene were the dominant PAHs and accounted for approximately 75 % of the total PAHs. The similar composition characteristics of PAHs and the significant correlations among individual, low molecular weight, high molecular weight, and total PAHs were found in all six sampling site types, thus indicating that PAHs originated from similar sources. The results of both isomeric ratios and principal component analyses confirmed that PAHs were mainly derived from the incomplete combustion of e-waste. The former open burning sites and dismantling sites were the main sources of PAHs. Soil samples that were taken closer to the point sources had high PAH concentrations. PAHs are transported via different soil profiles, including those in agricultural fields, and have been detected not only in 0- to 40-cm-deep soil but also in 40 cm to 80 cm-deep soil. PAH concentrations in soils in Longtang have been strongly affected by primitive e-waste recycling, particularly by former open burning activities.     

Characterization of an urban landfill soil by using physicochemical analysis and solid phase microextraction (SPME)—GC/MS

We have aimed at characterizing top soil samples taken in-situ from five different locations of the unregulated dumping site in Eskişehir/Turkey for a period of six months. The study is the first attempt in the city and in Turkey, regarding particularly the SPME (Solid Phase Microextraction Technique) analysis method utilized. A comprehensive research has been conducted to produce critical soil data to be used for indicating current risks as well as the urgency of rehabilitating the site and establishing a sanitary landfill in the site. Conventional physicochemical analytical methods and SPME technique were used to analyze the samples. Physicochemical analyses were performed for determining the pH, total dried matter, volatile matter, total nitrogen, phosphorus, macro elements and heavy metals. Meteorological data were also recorded for the same period. SPSS.10.0 statistical program was used to determine the correlation between meteorological data and physicochemical analysis results. Mean values were used in the correlation analyses. These data indicated that the air temperature and precipitation have significant effects on soil characteristics. SPME, coupled with GC/MS, was used to identify eighty six volatile and semi-volatile organic compounds contained in soil samples. The samples were extracted by headspace SPME with heating (δHS-SPME). SPME analyses were conducted using a commercially available polydimethylsiloxane/divinylbenzene (PDMS/DVB) fiber having a film thickness of 65 μm (Supelco) as a capture medium. The experimentally optimized headspace sampling conditions were arranged (15 min. at 50^˚C) before a 30 min. sampling period.     

Frequency Analysis for Precipitation Events and Dry Durations of Virginia

Stormwater Control Measures (SCMs) are widely used to control and treat stormwater runoff pollution. The first step in SCM design is to evaluate the precipitation patterns at a site. SCMs are normally designed using a storm with a specific return period. A robust design process that uses frequency distribution of precipitation and monitoring of performance could improve our understanding of the behavior and limitations of a particular design. This is not the current norm in the design of SCMs. In this research, frequency analyses (FA) of precipitation events was conducted using hourly precipitation data from 1948 to 2010 for eight sites representing the four major physiographic regions of Virginia. The available data were treated using an inverse distance method to eliminate missing gaps before processing into events determined by minimum inter-event times. FA was at each site to develop frequency plots of precipitation and dry duration. FA of the eight locations indicates a range of rainfall depths from 22.9 mm in Bristol to 35.6 mm in Montebello, compared to the nominal “water quality storm” of 25.4 mm (i.e., 1 in.). Similarly, for dry duration, for a 10 % exceedance probability, the range is from 16.8 days in Richmond and Norfolk to 19.5 days in Montebello. Dry duration provides guidance for vegetation selection, which is important for some SCMs. The degree of variability in both parameters argues for consideration of site-specific information in design. FA was also used to provide guidance to improve monitoring programs. Monte Carlo simulations demonstrated that performance monitoring programs applied in different regions would likely encounter more than 30 % of precipitation events less than 6.35 mm, and 10 % over 25.4 mm under various sampling regimes. The percentages of precipitation events encountered in the Coastal Plain and Piedmont regions are not impacted by sampling regimes, however the Blue Ridge Mountains and Valley and Ridge regions are likely impacted. Anticipating event occurrences improves the chances of implementing a successful monitoring program. The use of these results could enhance the performance of SCMs with consideration of local conditions for both monitoring SCMs and their design basis.     

Evaluation of a novel hollow fiber membrane technique for collection of 1,1-dimethylhydrazine in air

The purpose of this study was to develop a novel one-step method for the time-weighted average determination of 1,1-dimethylhydrazine (UDMH) in the air followed by spectrophotometric detection. For this reason, 0.1% hydrochloric acid as the absorbent was used in hollow fiber (HF) membrane for sampling of UDMH from an atmospheric standard chamber. Response surface methodology (RSM) with central composite design (CCD) was used to optimize the sampling parameters, such as flow rate and sampling time. Moreover, several analytical parameters including breakthrough (BT) volume, storage time, and carryover effect of the proposed HF were investigated. The results showed that optimal sampling rate was 9.90 mL/min. In order to validate the proposed method, it was compared with the National Institute for Occupational Safety and Health (NIOSH) 3515 method, which showed good compatibility between the two methods. Intra- and inter-day repeatability values of the HF method were in the range 0.082–0.1 and 0.091–0.12, respectively, and the limits of detection (LODs) and limits of quantitation (LOQs) were 0.002 and 0.006 ng/mL, respectively. The storage time of the proposed HF was 7 days at 2 °C. These results demonstrated that the one-step HF membrane offered a high sensitivity for sampling of UDMH in air.     

Speciation of As(III) and As(V) in water and sediment using reverse-phase ion-pair high-performance liquid chromatography-neutron activation analysis (HPLC-NAA)

Total As content and the As species distribution in water and sediments from the Kwabrafo stream, a major water body draining the Obuasi gold mining community in southwestern Ghana, have been investigated. Total As content was determined by instrumental neutron activation analysis (INAA). Ion-pair reverse phase high-performance liquid chromatography-neutron activation analysis (HPLC-NAA) was used for speciation of As species. Solid phase extraction with phosphate buffer was used to extract soluble As species from lyophilized sediment. The mass balance after phosphate extraction of soluble As species in sediment varied from 89 to 96 %. Compositionally appropriate reference material International Atomic Energy Agency (IAEA)-Lake Sediment (SL)-1 was used to check the validity of INAA method for total As determination. The measured values are in good agreement with the IAEA recommended value and also within the 95 % confidence interval. The accuracy of the measurement in terms of relative deviation from the IAEA recommended value was ±0.83 %. “In-house” prepared As(III) and As(V) standards were used to validate the HPLC-INAA method used for the As species determination. Total As concentration in the water samples ranged from 1.15 to 9.20 mg/L. As(III) species in water varied from 0.13 to 0.7 mg/L, while As(V) species varied from 0.79 to 3.85 mg/L. Total As content in sediment ranged from 2,134 to 3,596 mg/kg dry mass. The levels of As(III) and As(V) species in the sediment ranges from 138 to 506 mg/kg dry mass and 156 to 385 mg/kg dry mass, respectively.     

Assessment of organochlorine pesticides and plasticisers in the Selangor River basin and possible pollution sources

A study on the quality of water abstracted for potable use was conducted in the Selangor River basin from November 2008 to July 2009. Seven sampling sites representing the intake points of water treatment plants in the basin were selected to determine the occurrence and level of 15 organochlorine pesticides (OCPs), six phthalate esters (PAEs) and bisphenol A (BPA). Results indicated OCPs were still detected regularly in 66.1 % of the samples with the Σ₁₅OCPs ranging from 0.6–25.2 ng/L. The first data on PAEs contamination in the basin revealed Σ₆PAEs concentrations were between 39.0 and 1,096.6 ng/L with a median concentration of 186.0 ng/L while BPA concentration ranged from <1.2 to 120.0 ng/L. Although di-n-butyl phthalate was detected in all the samples, concentrations of di-ethyl(hexyl)phthalate were higher. Sampling sites located downstream recorded the highest concentrations, together with samples collected during the dry season. Comparison of the detected contaminants with the Department of Environment Water Quality Index (DOE-WQI) showed some agreement between the concentration and the current classification of stream water. While the results suggest that the sites were only slightly polluted and suitable to be used as drinking water source, its presence is cause for concern especially to the fragile firefly “Pteroptyx tener” ecosystem located further downstream.     

食品企业周边空气中异味挥发性有机物测定方法比较

以1个典型食品生产企业(酱菜厂)周边的异味挥发性有机物监测为例,介绍了罐采样-GC/MS、便携式GC/MS、SPME-GC/MS以及SPME-异味分析系统等4种监测方法的实际应用,从定性、定量监测结果等方面,比较了4种监测方法的特点。罐采样-GC/MS、便携式GC-MS 2种方法适用于定性、定量检测,在有标准样品的前提下,定量结果总体可比;SPME-GC/MS以及SPME-异味分析系统2种方法更适用于定性检测。     

Contributions of dry and wet depositions of polychlorinated dibenzo-p-dioxins and dibenzofurans to a contaminated site resulting from a penetachlorophenol manufacturing process

The soils at a factory for manufacturing pentachlorophenol were heavily contaminated by polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). In order to verify the contributions of dry and wet deposition of PCDD/Fs from the ambient air, the concentration of PCDD/Fs in ambient air and soil were measured, the partition of particle- and gas-phases of atmospheric PCDD/Fs was calculated, and the annual fluxes of total dry and wet PCDD/F depositions were modeled. Average atmospheric PCDD/F concentration was 1.24 ng Nm^???3 (or 0.0397 ng I-TEQ Nm^???3). Moreover, over 92.8% of total PCDD/Fs were in the particle phase, and the dominant species were high chlorinated congeners. The total PCDD/F fluxes of dry and wet deposition were 119.5 ng m^???2 year^???1 (1.34 ng I-TEQ m^???2 year^???1) and 82.0 ng m^???2 year^???1 (1.07 ng I-TEQ m^???2 year^???1), respectively. By scenario simulation, the total fluxes of dry and wet PCDD/F depositions were 87.1 and 68.6 ng I-TEQ, respectively. However, the estimated PCDD/F contents in the contaminated soil were 839.9 ?? g I-TEQ. Hence, the contributions of total depositions of atmospheric PCDD/F were only 0.02%. The results indicated that the major sources of PCDD/F for the contaminated soil could be attributed to the pentachlorophenol manufacturing process.     

连续流动注射间接测定空气中的五氧化二磷

建立连续流动注射间接测定空气中五氧化二磷的方法。空气中的五氧化二磷用过氯乙烯滤膜或滤筒采样,加入去离子水反应生成正磷酸,过滤、洗涤、定容后运用连续流动注射仪进行测定。优化了抗坏血酸浓度、硫酸浓度、钼酸盐浓度以及恒温室温度等影响显色的因素。最佳条件下,实际样品五氧化二磷加标回收率为96.0%~102%,相对标准偏差在4%以下;采样体积为300 L时,方法检出限为0.001 6 mg/m~3。t检验结果表明,所建方法与现行国标法的测定结果无显著性差异。方法分析速度快、重现性好、灵敏度高,适用于空气中五氧化二磷的测定。     

Pristine aquatic systems in a Long Term Ecological Research (LTER) site of the Brazilian Cerrado

The maintenance of limnological monitoring programs in the Cerrado Domain is crucial as a provision of useful information about temporal variations in land use and their respective water quality responses, considering its importance as water source for different Brazilian hydrographic basins. The purpose of this research was to describe limnological variables of low-order lotic systems located in the Cerrado Long Term Ecological Research (LTER) site (Environmental Protection Area (APA) Gama and Cabeça de Veado, Federal District of Brazil). Altogether, nine different streams were considered in this study. Samplings were conducted between 2010 and 2012, concentrated in the dry and rainy seasons. The sampling sites were generally characterized by low nutrient concentrations (e.g., medians, TP?=?14.8 μg L^?1, TN?=?20.0 μg L^?1, NO₃?=?13.8 μg L^?1) and slightly acidic waters (median, pH?=?5.3), with quite low electrical conductivity values (median?=?6.4 μS cm^?1). However, water quality degradation as a response to diffuse pollution was reported in some sampling points (e.g., Onça and Gama streams), expressed by relatively higher N and P concentrations, which were probably highlighted by the good water quality of the data set as whole. Although there was a trend to higher values of nitrogen forms during the dry season, significant statistical differences between the seasonal periods were reported only for the variables temperature and dissolved silica, which were higher in the dry and rainy season, respectively. The streams located in the preserved areas inside the ecological stations of APA Gama and Cabeça de Veado can still be considered good examples of reference lotic systems in the Cerrado Domain; notwithstanding, this study reported incipient signs of water quality degradation which cannot be overlooked in future limnological monitoring.     

Occurrence and sorption properties of arsenicals in marine sediments

The content of total arsenic, the inorganic forms: arsenite (As(III)) and arsenate (As(V)), the methylated forms: monomethylarsonic acid and dimethylarsinic acid (DMA), trimethylarsenic oxide, tetramethylarsenonium ion and arsenobetaine was measured in 95 sediment samples and 11 pore water samples from the Baltic Sea near the island of Bornholm at depths of up to 100 m. As(III+V) and DMA were detected in the sediment and As(III+V) was detected in the sediment pore water. Average total As concentration of 10.6?±?7.4 mg/kg dry matter (DM) in the sediment corresponds to previously reported values in the Baltic Sea and other parts of the world. Existing data for on-site measurements of sorption coefficients (Kd) of arsenicals in marine and freshwater sediments show large variability from <1 to >1,000 L/kg. In this work, calculated sorption coefficients (Kd and Koc) for As(III+V) showed significant correlation with depth, dissolved oxygen (DO), salinity and sediment classification; for depths <70 m, salinity <11 %, DO >9 mg/L and sand/silt/clay sediments the Kd was 118?±?76 L/kg DM and for depths >70 m, salinity >11 %, DO?<?9 mg/L and muddy sediments the Kd was 513?±?233 L/kg DM. The authors recommend using the found Kd value for arsenic in marine sediments when conditions are similar to the Baltic Sea. At locations with significant anthropogenic point sources or where the local geology contains volcanic rock and sulphide mineral deposits, there may be significantly elevated arsenic concentrations, and it is recommended to determine on-site Kd values.     

Application of portable gas chromatography-photo ionization detector combined with headspace sampling for field analysis of benzene, toluene, ethylbenzene, and xylene in soils

A method based on headspace (HS) sampling coupling with portable gas chromatography (GC) with photo ionization detector (PID) was developed for rapid determination of benzene, toluene, ethylbenzene, and xylenes (BTEX) in soils. Optimal conditions for HS gas sampling procedure were determined, and the influence of soil organic matter on the recovery of BTEX from soil was investigated using five representative Chinese soils. The results showed that the HS-portable-GC-PID method could be effectively operated at ambient temperature, and the addition of 15 ml of saturated NaCl solution in a 40-ml sampling vial and 60 s of shaking time for sample solution were optimum for the HS gas sampling procedure. The recoveries of each BTEX in soils ranged from 87.2 to 105.1 %, with relative standard deviations varying from 5.3 to 7.8 %. Good linearity was obtained for all BTEX compounds, and the detection limits were in the 0.1 to 0.8 μg kg^?1 range. Soil organic matter was identified as one of the principal elements that affect the HS gas sampling of BTEX in soils. The HS-portable-GC-PID method was successfully applied for field determination of benzene and toluene in soils of a former chemical plant in Jilin City, northeast China. Considering its satisfactory repeatability and reproducibility and particular suitability to be operated in ambient environment, HS sampling coupling with portable GC-PID is, therefore, recommended to be a suitable screening tool for rapid on-site determination of BTEX in soils.     

Ecological vulnerability: seasonal and spatial assessment of trace metals in soils and plants in the vicinity of a scrap metal recycling factory in Southwestern Nigeria

The concentrations of selected heavy metals in the soil and vegetation in the immediate vicinity of a metal scrap recycling factory were determined in the dry and wet seasons using the Atomic Absorption Spectrophotometer. The results showed that the soil pH in all the sites indicated slight acidity (from 5.07 to 6.13), high soil organic matter content (from 2.08 to 5.60 %), and a well-drained soil of sandy loam textural composition. Soil heavy metal content in the dry season were 0.84–3.12 mg/kg for Pb, 0.26–0.46 mg/kg for Cd, 9.19–24.70 mg/kg for Zn, and 1.46–1.97 mg/kg for Cu. These values were higher than those in the wet season which ranged from 0.62–0.69 mg/kg for Pb, 0.67–0.78 mg/kg for Cd, 0.84–1.00 mg/kg for Zn, and 1.26–1.45 mg/kg for Cu. Except for cadmium in the dry season, the highest concentrations occurred in the northern side of the factory for all the elements in both seasons. An increase in the concentrations of the elements up to 350 m in most directions was also observed. There was no specific pattern in the level of the metals in the leaves of the plant used for the study. However, slightly elevated values were observed in the wet season (Pb 0.53 mg/kg, Cd 0.59 mg/kg, Cu 0.88 mg/kg) compared with the dry season values (Pb 0.50 mg/kg, Cd 0.57 mg/kg, Cu 0.83 mg/kg). This study showed that the elevated concentrations of these metals might be associated with the activities from the recycling plant, providing the basis for heavy metal pollution monitoring and control of this locality that is primarily used for agricultural purposes.