Journal of Environmental Monitoring最新文献

Leather tanneries around the world, including China, introduce chromium (Cr) and other metals into the environment. In China, the population pressure compels the utilization of every piece of available land for food production. In this study, we investigated the content, leachability and possible storage sinks for Cr and other metals in soils around facilities of leather industry in southern China. It was found that Cr in soils impacted by tannery can be as high as 2484 mg Cr kg⁻¹ soil, and the mean contents of other metals such as Zn (214 mg Zn kg⁻¹ soil), Cd (5.4 mg Cd kg⁻¹ soil), As (17 mg As kg⁻¹ soil) exceeded the soil quality standards and guidelines in China and Canada. Simulated leaching studies (i.e., Synthetic Precipitation Leaching Procedure) indicated that these soils could release Cr and other metals in concentrations above the environmental quality guidelines and standards for water in China and Canada. As a result, the mobility of metals from these soils can potentially contaminate both groundwater and surface water. We also found differential leachability of metals with soil properties such as total metal and total carbon contents. Principal component analysis of the total contents of 32 elements showed that the possible major sinks for Cr are organic matter and oxides of Fe/Mn/Al, while sulfates and phosphates are potential storage of Cd, Zn, Cu and Pb. The information obtained from this study can be valuable for the restoration of ecosystem functions (i.e., food production) in the study area.

494 smelter employees from New Brunswick participated in a bone lead survey conducted by McMaster University in 2008, using the four element "clover-leaf" geometry germanium detector system. The employees were measured at two different bone sites, tibia and calcaneus, each measurement lasting 30 minutes. Scattered photons, including Pb X-rays, were collected by the germanium detectors located behind the ¹⁰⁹Cd source. A strong positive correlation was observed between tibia and calcaneus lead concentrations. Having been provided with blood lead levels, a cumulative blood lead index (CBLI) was generated. The employees were classified into four groups based on their date of hire, and their CBLI levels were compared to their tibia and calcaneus lead concentrations in the different groups. The slopes of bone Pb versus CBLI varied amongst groups, with those hired earliest showing the steepest slopes. This could be taken to imply a non-linearity in the uptake of Pb by bone from blood. In this paper, the association of the bone lead concentrations versus CBLI has been expressed by a polynomial function for the whole group of employees.

The size, morphology and chemical composition of 37,715 individual particles collected over 22 sampling days in the vicinity of a large integrated steel production were studied by scanning and transmission electron microscopy. Based on the morphology, chemistry and beam stability the particles were classified into the following fourteen groups: silicates, sea salt, calcium sulfates, calcium carbonates, carbonate-silicate mixtures, sulfate-silicate mixtures, iron oxides, iron mixtures, metal oxide-metals, complex secondary particles, soot, Cl-rich particles, P-rich particles, and other particles. The majority of iron oxide (≈85%) and metal oxide-metal (≈70%) particles as well as ≈20% of the silicate particles are fly ashes from high temperature processes. The emissions from the steel work are dominated by iron oxide particles. For source apportionment, seven source categories and two sectors of local wind direction (industrial and urban background) were distinguished. In both sectors PM₁₀ consists of four major source categories: 35% secondary, 20% industrial, 17% soil and 16% soot in the urban background sector compared to 45% industrial, 20% secondary, 13% soil, and 9% soot in the industrial sector. As the secondary and the soot components are higher in the urban background sector than in the industrial sector, it is concluded that both components predominantly originate from urban background sources (traffic, coal burning, and domestic heating). Abatement measures should not only focus on the steel work but should also include the urban background aerosol.

Xiamen is one of China's most rapidly developing metropolises. The objectives of the present study were: (1) to establish the levels and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in soil across the Xiamen metropolis, (2) to evaluate the extent to which PAH concentrations were elevated in the high urbanization area (HUA) of the island and how these compared with those in the low urbanization area (LUA) of the mainland, and (3) to evaluate the PAH hazard based upon their Carcinogenic Potential (CP), defined as toxicity equivalence of ∑PAHs. Twenty two alternative relative carcinogenic potency schemes were used and compared. Results demonstrated PAH concentrations to be greatly elevated across the entire metropolis. Significantly, the most enriched compounds represented the greatest concern with respect to carcinogenicity. The CP of more than 25% of the industrial samples from the island surpassed the Canadian guidance threshold value (600 μg kg⁻¹) for an excess lifetime cancer risk (ELCR) of 1 in 10⁻⁶. While soil samples from the remaining land uses on the island were all below this threshold, PAH levels in soil were nonetheless elevated (enrichment factors of between 4.1 ± 1.9 and 16.3 ± 12.4 in the HUA, and between 1.3 ± 0.7 and 10.8 ± 4.4 in the LUA). Results relating to agricultural locations on the island indicated 75% of the samples in HUA and 28% of the samples in LUA to be above the USEPA guidance value for BaP (15 μg kg⁻¹). Given the exceptionally high population density on the island there is a need for further research to evaluate multiple pathway PAH exposure risks.

Oil spills relating to shipping incidents remain of substantial concern with respect to marine pollution. Whilst most frequently a reactive approach is adopted in post-incident monitoring (for the specific product involved), this paper reports important physical and compositional characteristics of commonly transported oils and oil products to afford pro-active assessments. These properties include specific gravity, viscosity, elemental composition and, of particular relevance, the relative class compositions between aliphatics, aromatics, resins and asphaltenes. The latter were determined experimentally using thin layer chromatography with flame ionization detection. Diagnostic ratios of specific compounds are reported, statistically analysed, and their significance in identification of different oil types and the weathering processes is discussed. The influence of the properties on fates under different environmental conditions (selected to represent contrasting European regional seas) are examined using the NOAA Automated Data Inquiry for Oil Spills (ADIOS2) model. Relative contributions of the different environmental conditions and properties to the fate of the oil at sea are discussed.

Atmospheric concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs), and polybrominated diphenyl ethers (PBDEs) were measured in Taizhou, a large electronic equipment waste (e-waste) recycling area in East China. The mean concentrations (in summer and winter) of PCDD/Fs (0.45 and 0.39 pg WHO-TEQ m⁻³, where WHO-TEQ is the toxic equivalent set by the World Health Organisation), PBDD/Fs (0.22 and 0.18 pg WHO-TEQ m⁻³), and PBDEs (270 and 225 pg m⁻³) in this region have declined compared with those in 2005, due to regulations on primitive e-waste recycling activities. However, these concentrations remain higher than the historically highest levels in Europe and North America. The congener profiles of 2,3,7,8-substituted PCDD/Fs were similar, with OCDD, 1,2,3,4,6,7,8-HpCDF, OCDF, and 1,2,3,4,6,7,8-HpCDD being the most abundant congeners at all sites. The PCDD/F homologue profiles in the present study were different from those typically observed at non-e-waste locations, indicating a distinct source in this region. Seasonal differences were found in the lower brominated PBDE profiles. These differences indicate that the PBDE emission sources in summer (e.g., strong evaporation sources) differed from those in winter. However, the relatively steady congener profiles of the highly brominated PBDEs suggest that these PBDEs were controlled primarily by similar emission mechanisms. The lifetime excess cancer risks from exposure to PCDD/Fs and PBDD/Fs via inhalation ranged from 0.7 × 10⁻⁵ to 5.4 × 10⁻⁵, or approximately 80 cancer cases in the Taizhou population.

An automated near infra-red (IR) continuous wave cavity ring down spectrometer with sample preconcentration has been developed for the measurement of ethene (C₂H₄) in air. The spectrometer incorporated a distributed feedback diode laser operating at wavelengths λ∼ 1.6 μm and a pre-concentration system containing an adsorbent, molecular sieve 4A (MS4A). An absorption line located at 6148.58 cm⁻¹, and free from spectral overlap with other atmospheric molecules, was used for ethene detection. The spectrometer has a capacity for determination of atmospheric ethene mixing ratios at half hour time intervals, with a detection limit (2 SD above baseline noise) of 280 ppt. Both weekday and weekend measurements were performed in ambient air for periods of up to 30 hours. Average daytime mixing ratios of ethene were observed to be 2 ppbv and 1 ppbv during weekdays and weekends respectively. The mixing ratios of ethene varied from 0.6 ppbv to 1.2 ppbv in Bristol air during the weekend, with influence of meteorological conditions. The observed variations are discussed with consideration of probable sources and various meteorological parameters. A correlation is observed in the mixing ratio of ethene and nitrogen dioxide.

¹³⁷Cs is one of the conservative tracers applied to the study of oceanic circulation processes on decadal time scales. To investigate the spatial distribution and the temporal variation of ¹³⁷Cs concentrations in surface seawater in the North Pacific Ocean after 1957, a technique for optimum interpolation (OI) was applied to understand the behaviour of ¹³⁷Cs that revealed the basin-scale circulation of Cs ¹³⁷Cs in surface seawater in the North Pacific Ocean: ¹³⁷Cs deposited in the western North Pacific Ocean from global fallout (late 1950s and early 1960s) and from local fallout (transported from the Bikini and Enewetak Atolls during the late 1950s) was further transported eastward with the Kuroshio and North Pacific Currents within several years of deposition and was accumulated in the eastern North Pacific Ocean until 1967. Subsequently, ¹³⁷Cs concentrations in the eastern North Pacific Ocean decreased due to southward transport. Less radioactively contaminated seawater was also transported northward, upstream of the North Equatorial Current in the western North Pacific Ocean in the 1970s, indicating seawater re-circulation in the North Pacific Gyre.

Selection of sampling device, sampling location and period are important first steps in the measurement of exposure to bioaerosols in indoor air. The steps following the sampling include treatment of samples and laboratory analysis. In this study, settling bacteria, endotoxin, fungi and serine protease have been measured in Danish homes using Electrostatic Dust Fall Collectors (EDCs). The effects of the presence of occupants, sampling on open surfaces versus in bookcases and treatment of samples have been studied. Concentrations of bacteria and endotoxin were significantly higher when occupants were at home than when they were absent. Across homes, higher concentrations of fungi were found in spring than in winter, as was the total inflammatory potential, while higher concentrations of protease were found in winter than in spring. The placement of the EDCs in bookcases versus on an open surface significantly affected the measured concentrations of bacteria and endotoxin. Direct extraction of EDC cloths caused a higher measured concentration of bacteria, fungi and serine protease than if EDC cloths were extracted post-storage at -20 °C. Extraction of EDC cloths caused an average of 51% and 58% extraction of bacteria and fungi respectively. In conclusion, EDCs should be placed on open surfaces during the sampling, how much occupants are present in their home during sampling and sampling season should be considered, EDC cloths should not be stored in a freezer before extraction of microorganisms, but extraction suspensions can be stored at -80 °C without affecting the number of microorganisms significantly.

Optimization of a water quality network through a change in sampling frequency is the only way to increase cost-efficiency without any reduction in the robustness of the data. Existing techniques define optimal sampling frequency based on analysis of historical data from the monitoring network under investigation. Their application to a large network comprised of many sites and many monitored parameters is both technical and challenging. This paper presents a simple non-parametric method for reviewing sampling frequency that is consistent with highly censored environmental data and oriented towards reduction of sampling frequency as a cost-saving measure. Based on simple descriptive statistics, the method is applicable to large networks with long time series and many monitored parameters. The method also provides metrics for interpretation of newly collected data, which enables identification of sites for which a future change in sampling frequency may be necessary, ensuring that the monitoring network is both current and adaptive. Application of this method to the New Zealand National Groundwater Monitoring Programme indicates that reduction of sampling frequency at any site would result in a significant loss of information. This paper also discusses the potential for reducing analysis frequency as an alternative to reduction of sampling frequency.