Influence of local and regional Mediterranean meteorology on SO₂ ground-level concentrations in SE Spain

This work presents the results of a 4-year study on sulfur dioxide (SO(2)) ground-level concentrations in an area of southeastern Spain, the L'Alacantí region, where the cement industry is important and coke use extends to other industries as well. The main source of SO(2) emissions in the area was found to be a the Lepold cement plant (one of the two cement plants in the area). The high levels of SO(2) probably extend back to 1920 when this plant began operations. Both local and Mediterranean-scale meteorological processes influence the SO(2) ground-level concentration and together explain the dispersion dynamics of this pollutant. The location and topography of the study zone result in NW Atlantic advections and E-SE sea breezes being the dominant atmospheric circulation patterns in the area. Under stable meteorological conditions, minor local circulations are also relevant to the SO(2) concentration levels. The high frequency of local circulations determines a concentration pattern that changes during the day, with impacts occurring preferentially in a W-NW direction from the source at midday (sea breeze and strong thermal mixture), and in a SE direction at night. This causes the SO(2) concentrations to present well-defined diurnal cycles with well-differentiated shapes depending on the location of the sampling station relative to the source. The dependence of SO(2) 10 min levels on the wind origin and speed throughout the day has been evaluated by studying statistical parameters including P95, P50 and arithmetic mean. Exceedances occur under specific dispersion conditions at distances less than 1 km from the source. However, the source is traceable at larger distances and the levels are higher than typical urban ones. P95 was used as an estimator of the occurrence of larger levels or impacts. Leeward of NW winds and the source, at night and in early morning, P95 levels are comprised between 30 and 55 μg m(-3). In contrast, with SE winds and at midday, P95 levels stay at 17 μg m(-3). The same P95 was obtained for winds lower than 5 m s(-1), which represent 89% of the winds in the area. However, stronger winds can have P95 levels above 125 μg m(-3).     

Mercury contamination-what we have learned since Minamata

Atmospheric cycling of mercury and other pollutants has become a major concern as industrialized countries have eliminated point discharges, sometimes by relocating the industries to underdeveloped and developing countries where point sources have become problems. Such circumventions may be to no avail in the long run as pollution continues to elevate levels of methylmercury in fish in waterways that are remote from direct contamination as well as where the source can be readily identified. Much has been learned about the cycling of mercury in the environment since human disabilities and deaths at Minamata, Japan, initially drew attention to the problem of methylmercury poisoning from the consumption of contaminated seafood in the 1950s. In that instance, methylmercury produced industrially concentrated to toxic levels in fish. As this manufacturing process was not used outside Japan, concern did not become immediate in other developed nations until the 1960s when it was established that mercury was not only biomethylated by microorganisms but also biomagnified through the food chain. Point sources to the waterways may have been eliminated too late to return the levels in fish to background because of the geochemical cycling of mercury through the environment. Despite decreases in domestic, industrial and agricultural point source releases over the last two decades, large quantities from non-point sources such as fossil fuel combustion, smelters, and incinerators are still being released. Much of this mercury is transported from the atmosphere to aquatic ecosystems and stored in sediments until it is again released to the water and atmosphere.     

The use of leeches to monitor aquatic PCB contamination at Mid-Canada radar line site 050: Four years post-remediation

The Mid-Canada Radar Line (MCRL) was built by the Canadian government during the 1950s and closed in the 1960s. MCRL Site 050 located in close proximity to Fort Albany First Nation was a source of polychlorinated biphenyls (PCBs); thus, this site was remediated in 2001. There has been concern in Fort Albany that the Albany River by MCRL Site 050 is still contaminated. We examined whether the aquatic environment surrounding MCRL Site 050 has returned to background levels four years post-remediation using leeches (Haemopis spp.) as bioindicators. Leech data for 2005 indicates that PCB levels remain higher near Site 050 than at the control site upstream; however, there has been a decrease in difference between Site 050 and the control site for leech body burden between years. Thus, the removal of the terrestrial source of PCB contamination at Site 050 appears to have removed the main source of aquatic PCBs.     

Presence and partitioning properties of the flame retardants pentabromotoluene, pentabromoethylbenzene and hexabromobenzene near suspected source zones in Norway

The brominated flame retardants (BFRs), pentabromotoluene (PBT), pentabromoethylbenzene (PBEB) and hexabromobenzene (HBB), exhibit physical-chemical properties similar to other persistent organic pollutants, and have been in use as flame retardants for several decades. Data on these BFRs in diverse environmental samples can be found in studies from the 1970s and 1980s, as well as in recent years, though very little in the years in between. Due to a lack of data, the cause for the apparent re-emergence of these BFRs in recent studies is unclear, and could reflect changes in production volumes, accumulation of transformation products from BFR precursors, improved analytical techniques or simply a re-emergence in concern. Very little data are available on their environmentally relevant partitioning properties, which could help to explain the occurrence and fate of these BFRs. In this study we analysed for the presence of HBB, PBT, and PBEB in diverse environmental samples from potential Norwegian BFR source zones. Additionally, environmental partitioning properties of these BFRs as well as brominated benzenes were estimated and validated using experimental data for brominated benzenes. Of the three BFRs, HBB was identified in detectable quantities at most source zones, PBEB only near a metal recycling factory, and PBT only in a few additional locations from where PBEB was detected. Data from this study show that HBB is likely widely distributed, as verified both by chemical analysis and estimated properties. Measured HBB levels in wastewater treatment plants indicate that the treatment practices used in the study locations are not effective at lowering HBB levels, perhaps due to association with low density suspended solids (e.g. microplastics).     

Polychlorinated biphenyls in two salt marsh sediments of the Venice Lagoon

Polychlorinated biphenyls (PCBs) were measured in two dated salt marsh cores of the Venice Lagoon to assess their input chronology and to evaluate the importance of atmospheric deposition as a source. Sampling sites were chosen in order to evidence the differences between areas located leeward and windward with respect to inputs originating in both the city of Venice and the industrial area. Concentrations of PCB indicators (0.13-15.6 ng g?1) increased gradually from the 1930s, reached maxima from the 1950s to the late 1970s, and then decreased. PCB loadings to marshes are driven by both the atmospheric deposition and the resuspension of subtidal sediments, this latter being more important for heavier congeners. The downwind marsh recorded higher fluxes (0.06-9.72 ng cm?2 year?1) than the upwind one (0.01-0.53 ng cm?2 year?1). Recent fluxes are rather consistent with bulk deposition measurements. A higher contribution of CB-101 and CB-118 was detected in the intermediate layers of the downwind site, suggesting a different PCB source for the corresponding time interval. In the other marsh, PCBs showed a rather constant composition at all levels (mostly CB-153, CB-138 and CB-180), accounting for a regional influence. Deep layers showed an enrichment of higher chlorinated congeners at both sites, whereas recent samples conserve the patterns typical of surficial and subsurficial subtidal sediments. The scientific approach adopted in this research can be considered as a sort of methodological procedure for the determination of fluxes and pathways of PCBs through the study of marsh cores.     

The history of hexachlorobenzene accumulation in Svalbard fjords

In the present study, we investigated the spatial and historical trends of hexachlorobenzene (HCB) contamination in dated sediments of three Svalbard fjords (Kongsfjorden, Hornsund, Adventfjorden) differing in environmental conditions and human impact. HCB concentrations ranging from below limit of quantification (6.86 pg/g d.w.) to 143.99 pg/g d.w. were measured. The highest concentrations were measured in two surface sediment layers of the core collected in Hornsund near the melting glacier. The lowest concentrations of HCB were measured in Adventfjorden, suggesting that local source of HCB is not significant and global transport processes are the major transport pathways. The history of HCB deposition did not fully reflect the history of HCB emission (largest in 1950s and 1960s). In case of several sediment cores, the HCB enrichment in surface (recent) sediments was noticed. This can indicate importance of secondary sources of HCB, e.g., the influx of HCB accumulated over decades on the surface of glaciers. Detected levels of HCB were generally low and did not exceed background concentration levels; thus, a negative effect on benthic organisms is not expected.     

The occurrence of the herbicide dalapon (2,2-dichloropropionate) in potable water as a disinfection by-product

Salts of 2,2-dichloropropionic acid, such as dalapon, are well known as herbicides and are regulated as such in potable water in Australia and elsewhere. It is also an identified disinfection by-product (DBP), but little is known about the compound's formation and typical levels from this source. This work presents results from a sampling campaign where 2,2-dichloropropionate was found at levels between 0.1 and 0.5 μg l(-1) in potable water samples from a major treatment plant in South East Queensland, Australia. However, levels were below the reporting limit (0.01 μg l(-1)) in the immediate source water for the plant. Also, temporal trends in 2,2-dichloropropionate observed in treated water during sampling mirrored those of trihalomethanes albeit at much lower concentrations, suggesting that the occurrence is due to in situ formation as a DBP. This could present a regulatory dilemma in some jurisdictions.     

The use of leeches and logit log-linear contingency models to assess and monitor aquatic PCB contamination originating from mid-Canada radar line site 050

Abandoned military sites in northern North America are relics of the Cold War and sources of polychlorinated biphenyls (PCBs). In the late 1990s, the Canadian federal and provincial governments began the cleanup of the mid-Canada radar line in Ontario, Canada. The first site to be remediated was Site 050 (Fort Albany First Nation) in 2001; however, the community remains concerned that contaminants may have moved prior to, during, and after remediation into the Albany River directly adjacent to Site 050. Thus, the Albany River was monitored (1999, 2001, 2002) during the remediation process to determine if the cleanup itself further contaminated the aquatic compartment, using leeches (Haemopis spp.) as bioindicators. Few organochlorines were found in leeches at levels higher than the detection limit, aside from PCBs. Leech data from the present study indicated that PCB levels were significantly higher near Site 050 than the control site upstream, indicating point source contamination from Site 050. The temporal trend in leech contaminant data indicated an increase in PCB contaminant load from 1999 (pre-remediation) to 2001 (immediately post-remediation), but this difference was not statistically significant due to high variances. Nevertheless, logit log-linear contingency modeling did reveal that immediately after cleanup (2001), contaminants (CBs 99, 118, 128, 156, 170, 183) in leeches were detected significantly more frequent than expected. When taken together, leech body burden and frequency of detection data suggest that the remediation process itself further contaminated the aquatic environment, if only temporarily. Lastly, the removal of the terrestrial source of PCBs during remediation did remove the source of aquatic contaminants in that body burden of contaminants in leeches were significantly lower a year after cleanup.     

Comparison of Nitrate Levels in Raw Water and Finished Water from Historical Monitoring Data on Iowa Municipal Drinking Water Supplies

Nitrate contamination of water sources is a concern where large amounts of nitrogen fertilizers are regularly applied to soils. Ingested nitrate from dietary sources and drinking water can be converted to nitrite and ultimately to N-nitroso compounds, many of which are known carcinogens. Epidemiologic studies of drinking water nitrate and cancer report mixed findings; a criticism is the use of nitrate concentrations from retrospective drinking water data to assign exposure levels. Residential point-of-use nitrate data are scarce; gaps in historical data for municipal supply finished water hamper exposure classification efforts. We used generalized linear regression models to estimate and compare historical raw water and finished water nitrate levels (1960s--1990s) in single source Iowa municipal supplies to determine whether raw water monitoring data could supplement finished water data to improve exposure assessment. Comparison of raw water and finished water samples (same sampling date) showed a significant difference in nitrate levels in municipalities using rivers; municipalities using other surface water or alluvial groundwater had no difference in nitrate levels. A regional aggregation of alluvial groundwater municipalities was constructed based on results from a previous study showing regional differences in nitrate contamination of private wells; results from this analysis were mixed, dependent upon region and decade. These analyses demonstrate using historical raw water nitrate monitoring data to supplement finished water data for exposure assessment is appropriate for individual Iowa municipal supplies using alluvial groundwater, lakes or reservoirs. Using alluvial raw water data on a regional basis is dependent on region and decade.     

General plume dispersion model (GPDM) for point source emission

Gaussian-based dispersion models are widely used to estimate local pollution levels. The accuracy of such models depends on stability classification schemes as well as plume rise equations. A general plume dispersion model (GPDM) for a point source emission, based on Gaussian plume dispersion equation, was developed. The program complex was developed using Java and Visual basic tools. It has the flexibility of using five kinds of stability classification schemes, i.e., Lapse Rate, Pasquill–Gifford (PG), Turner, σ–θ and Richardson number. It also has the option of using two types of plume rise formulations – Briggs and Holland’s. The model, applicable for both rural and urban roughness conditions, uses meteorological and emission data as its input parameters, and calculates concentrations of pollutant at the center of each cell in a predefined grid area with respect to the given source location. Its performance was tested by comparing with 4-h average field data of continuous releases of SO₂ from Dadri thermal power plant (Uttar Pradesh, India). Results showed that the Turner scheme used with Holland’s equation gives the best outcome having a degree of agreement (d) of 0.522.     

对应分析在大气颗粒物源解析中的应用研究

采用对应分析方法定性研究龙岩市大气颗粒物来源问题。结果表明:龙岩市4个监测点位中龙岩市环境监测站的主要污染源为高岭土矿和土壤风沙尘;龙岩学院与闽西职业技术学院的主要污染源为机动车尾气尘、燃煤尘和土壤风沙尘;龙岩师专的主要污染源为燃煤尘、小煤炉尘、水泥成品、水泥厂除尘器集尘和钢铁厂除尘器集尘。该方法能将R型因子分析和Q型因子分析结合起来,综合体现样品和元素之间的关系,为大气颗粒物源解析提供了一种新的途径。     

First study on anthropogenic Pt, Pd, and Rh levels in soils from major avenues of S?o Paulo City, Brazil

Over the last years, investigations on the increase of platinum (Pt), palladium (Pd), and rhodium (Rh) levels in urban environments of big cities all over the world - especially to catalytic converters emissions - have been grown up enormously. S?o Paulo City is the 6th largest megacity in the world having about 20 million inhabitants and an ever increasing seven million motor vehicle fleet. In spite of this, there has never been an investigation regarding Pt, Pd, and Rh levels in the city. In the present study, Pt, Pd, and Rh concentrations were determined in soils adjacent to seven main high-density traffic avenues in the metropolitan region of S?o Paulo City. Inductively coupled plasma mass spectrometry was employed - after ultrasound-assisted aqua regia leaching - as analytical technigue. The results showed concentration levels up to 378?ng?g^?1 for Pd, 208?ng?g^?1 for Pt, and 0.2 to 45?ng?g^?1 for Rh. These levels are much higher than those considered for the geochemical background of soils, indicating a catalytic converter source. Due to the different Pt/Pd/Rh ratio in Brazilian automobile catalytic converters, lower levels of Pt/Pd ratios compared with other similar studies were observed. The obtained results are the first data for monitoring Pt, Pd, and Rh pollution in S?o Paulo City soils.     

The Impact of Urbanization and Protection of Water Resources in Owerri and Environs SE, Nigeria

Untreated sewage and agriculture are the most important sources of contamination. The study was carried out by conducting a short-term surface water and groundwater pollution survey of the Owerri Urban area and its environs, in order to establish the current levels of pollution. An attempt has been made to show the relationships between pollution levels, population density, industrial and agricultural activities. The spatial distribution of pollutants due to a poor land use system and to human activities was investigated. This emphasises integrated planned development as a preventive measure for arresting pollution levels in fast growing urban centres. The total groundwater stored in the area amounts to 7.87 × 10⁹ m³. Twenty five percent of this is released as base flow into the adjacent rivers (Otamiri and Nworie). The annual groundwater recharge is 3.4 × 10⁹ m³. The enormous volume of groundwater stored and the comparatively low cost of development makes groundwater an excellent alternative supply source for the area (Uma et al., 1984).     

Thermogenic hydrocarbons in seawater of the Gippsland Shelf,southeast Australia

An offshore survey measured the concentration of thermogenic hydrocarbons (THCs) in samples extracted from seawater at 718 locations along 22 traverse lines across the Gippsland Shelf, southeast Australia, and recorded compounds typical of subsurface crude oil and natural gas (petroleum) accumulations. Background concentrations of 8 ppm, with isolated peak levels of 20 to 52 ppm, were detected in samples extracted from seawater at depths of 30 to 50 m over distances of 10 km. Two sources have been suggested — seepage of THCs from subsurface accumulations of petroleum, or THCs in waste-water discharged by several offshore petroleum production facilities which are present on the shelf. A waste-water source is favoured because of the transitory nature of the concentrations, and changes in composition consistent with plume drift away from the point(s) of discharge. Overall, however, the concentration of THCs in waters of the Gippsland Shelf compare favourably with levels in waters affected by urban runoff. The concentration of THCs in other coastal waters from urban and onshore sources is low, equivalent to the background concentration in the major oceans of the world.     

国家污染源监测数据管理系统构建

针对全国污染源监测数据管理和应用需求,设计了一套污染源监测数据指标集,分析了污染源排放达标评价对象及评价结果表征方法,突破了建立电子化排放标准库、数据录入全过程多层次质量控制等关键技术,并在需求分析、功能设计和技术方案选择的基础上,开发了覆盖国家、省、市3级应用的污染源监测数据管理信息软件平台,取得了很好的应用效果。     

Trace elements (Cu,Zn, and Hg) and δ<Superscript>13</Superscript>C/δ<Superscript>15</Superscript>N in seabird subfossils from three islands of the South China Sea and its implications

Seabird subfossils were collected on three islands of the Xisha Archipelago, South China Sea. Via elemental analysis, we identified that bird guano was a significant source for heavy metals Cu, Zn, and Hg. Cu and Zn levels in these guano samples are comparable to their levels in wildbird feces, but guano Hg was lower than previously reported. Trophic positions significantly impacted transfer efficiency of heavy metals by seabirds. Despite of a common source, trace elements, as well as stable isotopes (i.e., guano δ¹³C and collagen δ¹⁵N), showed island-specific characteristics. Bird subfossils on larger island had relatively greater metal concentrations and revealed higher trophic positions. Partition of element and isotope levels among the islands suggested that transfer efficacy of seabirds on different islands was different, and bird species were probably unevenly distributed among the islets. Island area is possibly a driving factor for distributions of seabird species.     

COPPER CONTENTS IN MEDITERRANEAN ECOSYSTEMS IN SOUTH AMERICA

Copper mining activities are very important in central Chile.Like other metals, copper is a nutrient for most plants at lowconcentration levels; however, at higher levels it may becometoxic. At present, copper abundance in mediterraneanecosystems is unknown both for vegetation and soils. In thisstudy, two localities of the Coastal Range in central Chilewere studied. Copper content was found to be mainly related tosite type, and secondly to the components of the ecosystem.Copper contents are similar to other mediterranean ecosystemsof the world. Soil was found to represent the main source ofdata variation.     

Use of the land snail Helix aspersa for monitoring heavy metal soil contamination in Northeast Algeria

The objective of this study was to investigate the impact of anthropogenic activities on soil quality using the land snail Helix aspersa as a bioindicator. Soil samples and snails were collected from several sites in Northeast Algeria during the summer and winter of 2010. All of the sites were chosen due to their proximity to industrial factories—a potential source of soil pollution via heavy metal contamination. The concentration of heavy metals (Pb, Cd, Mn, and Fe) in soil samples was analyzed using atomic absorption spectrophotometry. Activity levels of glutathione S-transferase (GST) and acetylcholinesterase (AChE), indicators of oxidative stress and neurotoxicity, respectively, were measured in snails collected from each site. GST and AChE activity were found to vary between sites and by season. The highest levels of GST activity were registered during the summer at sites closest to potential sources of pollution. AChE activity levels also peaked during the summer with the highest values recorded at the site in El Hadjar. These increased levels of bioindicative stress response correlated with increasing metal concentration in soil samples collected at each site.     

Evaluation of the urban/rural particle-bound PAH and PCB levels in the northern Spain (Cantabria region)

The aim of the present study was to evaluate the polycyclic aromatic hydrocarbon (PAH) and polychlorinated biphenyl (PCB) levels in PM(10) and PM(2.5), at one rural and three urban sites in the Cantabria region (northern Spain). From all of these pollutants, benzo(a)pyrene is regulated by the EU air quality directives; its target value (1?ng/m(3)) was not exceeded. The concentration values of the studied organic pollutants at the studied sites are in the range of those obtained at other European sites. A comparison between the rural-urban stations was developed: (a) PAH concentration values were lower in the rural site (except for fluorene). Therefore, the contribution of local sources to the urban levels of PAHs seems relevant. Results from the coefficient of divergence show that the urban PAH levels are influenced by different local emission sources. (b) PCB rural concentration values were higher than those found at urban sites. Because no local sources of PCBs were identified in the rural site, the contribution of more distant emission sources (about 40?km) to the PCB levels is considered to be the most important; the long-range transport of PCBs does not seem to be significant. Additionally, local PAH tracers were identified by a triangular diagram: higher molecular weight PAHs in Reinosa, naphthalene in Santander and anthracene/pyrene in Castro Urdiales. A preliminary PAH source apportionment study in the urban sites was conducted by means of diagnostic ratios. The ratios are similar to those reported in areas affected by traffic emissions; they also suggest an industrial emission source at Reinosa.     

Sources of PM10 and PM2.5 in Cairo’s ambient air

A source attribution study was performed to assess the contributions of specific pollutant source types to the observed particulate matter (PM) levels in the greater Cairo Area using the chemical mass balance (CMB) receptor model. Three intensive ambient monitoring studies were carried out during the period of February 21–March 3, 1999, October 27–November 27, 1999, and June 8–June 26, 2002. PM₁₀, PM_2.5, and polycyclic aromatic hydrocarbons (PAHs) were measured on a 24-h basis at six sampling stations during each of the intensive periods. The six intensive measurement sites represented background levels, mobile source impacts, industrial impacts, and residential exposure. Major contributors to PM₁₀ included geological material, mobile source emissions, and open burning. PM_2.5 tended to be dominated by mobile source emissions, open burning, and secondary species. This paper presents the results of the PM₁₀ and PM_2.5, source contribution estimates.