Determination of selected heavy metals in air samples from the northern part of Jordan

In this work, the atmospheric concentrations of selected heavy metals including lead (Pb), iron (Fe), cadmium (Cd), copper (Cu), nickel (Ni), manganese (Mn), and zinc (Zn) were measured for two different sampling sites (urban and rural) in the northern part of Jordan (Irbid city). Samples were collected according to a certain schedule for 1 year. High volume air samplers and glass fiber filters were used to collect the samples. Collected samples were digested using a mixture of analytical grade nitric acid and analytical grade hydrochloric acid, and analyzed to evaluate the levels of heavy metals by atomic absorption spectrophotometry. Six heavy metals (Pb, Fe, Cu, Ni, Mn, and Zn) were measured in all samples; the concentrations of Cd and Co were not detected in Irbid atmosphere by atomic absorption spectroscopy. The results were used to determine the levels of heavy metal pollutants in air, possible sources, and to compare the levels of selected heavy metals in the two studied sites. Aerosols from the rural site have lower concentrations for all the metals compared to those from the urban site. The daily and monthly variations of the elements were investigated. All heavy metals in urban and rural sites reached maximum concentrations in June, July, and August. This is consistent with the increased activities leading to particulate matter emission during the summer period. The enrichment factors with respect to earth crust and correlation coefficients of heavy metals were investigated to predict the possible sources of heavy metals in air.     

Contribution of primary and secondary sources to organic aerosol and PM2.5 at SEARCH network sites

Chemical tracer methods for determining contributions to primary organic aerosol (POA) are fairly well established, whereas similar techniques for secondary organic aerosol (SOA), inherently complicated by time-dependent atmospheric processes, are only beginning to be studied. Laboratory chamber experiments provide insights into the precursors of SOA, but field data must be used to test the approaches. This study investigates primary and secondary sources of organic carbon (OC) and determines their mass contribution to particulate matter 2.5 microm or less in aerodynamic diameter (PM2.5) in Southeastern Aerosol Research and Characterization (SEARCH) network samples. Filter samples were taken during 20 24-hr periods between May and August 2005 at SEARCH sites in Atlanta, GA (JST); Birmingham, AL (BHM); Centerville, AL (CTR); and Pensacola, FL (PNS) and analyzed for organic tracers by gas chromatography-mass spectrometry. Contribution to primary OC was made using a chemical mass balance method and to secondary OC using a mass fraction method. Aerosol masses were reconstructed from the contributions of POA, SOA, elemental carbon, inorganic ions (sulfate [SO4(2-)], nitrate [NO3-], ammonium [NH4+]), metals, and metal oxides and compared with the measured PM2.5. From the analysis, OC contributions from seven primary sources and four secondary sources were determined. The major primary sources of carbon were from wood combustion, diesel and gasoline exhaust, and meat cooking; major secondary sources were from isoprene and monoterpenes with minor contributions from toluene and beta-caryophyllene SOA. Mass concentrations at the four sites were determined using source-specific organic mass (OM)-to-OC ratios and gave values in the range of 12-42 microg m(-3). Reconstructed masses at three of the sites (JST, CTR, PNS) ranged from 87 to 91% of the measured PM2.5 mass. The reconstructed mass at the BHM site exceeded the measured mass by approximately 25%. The difference between the reconstructed and measured PM2.5 mass for nonindustrial areas is consistent with not including aerosol liquid water or other sources of organic aerosol.     

Formation of organic tracers for isoprene SOA under acidic conditions

The chemical compositions of a series of secondary organic aerosol (SOA) samples, formed by irradiating mixtures of isoprene and NO in a smog chamber in the absence or presence of acidic aerosols, were analyzed using derivatization-based GC–MS methods. In addition to the known isoprene photooxidation products 2-methylglyceric acid, 2-methylthreitol, and 2-methylerythritol, three other peaks of note were detected: one of these was consistent with a silylated-derivative of sulfuric acid, while the remaining two were other oxidized organic compounds detected only when acidic aerosol was present. These two oxidation products were also detected in field samples, and their presence was found to be dependent on both the apparent degree of aerosol acidity as well as the availability of isoprene aerosol. The average concentrations of the sum of these two compounds in the ambient PM_2.5 samples ranged from below the GC–MS detection limit during periods when the isoprene emission rate or apparent acidity were low to approximately 200 ng m^?3 (calibrations being based on a surrogate compound) during periods of high isoprene emissions. These compounds presently unidentified have the potential to serve as organic tracers of isoprene SOA formed exclusively in the presence of acidic aerosol and may also be useful in assessments in determining the importance and impact of aerosol acidity on ambient SOA formation.     

Externalities of Fugitive Dust

It is known that fugitive dust can cause human health and environmental problems, alone or in combination with other air pollutants. These problems are referred to as ‘external costs’ that have been traditionally ignored. However, there is a growing interest towards quantifying externalities to assist policy and decision-making. With this in mind, the present study aimed at discussing the environmental regulations that deal with fugitive dust, the impact of fugitive dust on human health and global climate system, and the available methods for calculating fugitive dust externalities. The damage cost associated with human health and global environmental problems was predicted based on the environmental strategy priority model. The damage cost estimated by the model ranged from 40 to 374 EUR/kg of emitted fugitive dust with a mean value of 120 EUR/kg of emitted fugitive dust. It was also found that PM_2.5 and PM₁₀ have contributed to about 60% and 36% of the estimated damage cost, respectively. The remaining 4% was attributed to both nitrate and sulfate aerosols.     

Application of geographically weighted regression model to analysis of spatiotemporal varying relationships between groundwater quantity and land use changes (case study: Khanmirza Plain,Iran)

Understanding the spatiotemporal relationships between land use/cover changes (LUCC) and groundwater resources is necessary for effective and efficient land use management. In this paper, geographically weighted regression (GWR) and ordinary least squares (OLS) models have been expanded to analyze varying spatial relationships between groundwater quantity changes and LUCC for three periods: 1987–2000, 2000–2010, and 1987–2010 in the Khanmirza Plain of southwestern Iran. For this purpose, TM images were used to generate LUCC (rainfed, irrigated, meadow, and bare lands). Groundwater quantity variables, including groundwater level changes (GLC) and groundwater withdrawal differences (GWD), were gathered from piezometric and agricultural wells data. The analysis of spatial autocorrelation (Moran’s I and local indicators of spatial association ) demonstrated that GWR has a better ability to model spatially varying data with very minimal clustering of residuals. The results R ² and corrected Akaike’s Information Criterion parameters revealed that the GWR has the lowest similarity in space and time in neighboring situations and it has the high ability to explain more variance in the LUCC as a function of the groundwater quantity changes. All results of the distribution of local R ² values from GWR confirm our assertion that there is a spatiotemporal relationship between types of land use and each of groundwater quantity variables within the region. According to the t test results from GWR, there are significant differences between the GLC and GWD and the land use types in different places of region in each of the three time series. The GWR results can help decision-makers to make appropriate decisions for future planning.     

Appearance of aldehydes in the surface layer of lake waters

The paper presents results concerning the changes in the content of aldehydes in samples of lake water collected near the lake surface. The study of lake waters was undertaken to explain which physicochemical parameters of the environment have the greatest influence on the level of aldehydes, which of the aldehydes are most often met in surface water and in what concentrations. We observed that formaldehyde, acetaldehyde, propanal, glyoxal, methylglyoxal and acetone were commonly present in surface water samples, while semi-volatile and poorly soluble aldehydes such as nonanal and decanal were observed seasonally. The contents of total aldehydes varied in a wide range, from 55 to 670 μg/l, and the concentration of total organic carbon varied significantly from 3 to 18 mg /l, but there was no evident correlation between them in all of samples. The total content of aldehydes did not depend on the meteorological parameters such as air temperature, UV radiation and ozone concentration; however, it was noted that the level of carbonyl concentration is related to the period of intense precipitation: in the period of very low precipitations, the highest contents of total aldehydes were determined in all of the water samples, and in the periods of intense precipitations, the content of total aldehydes was drastically smaller.     

Metals in sediments and mangrove oysters (Crassostrea rhizophorae) from the Caroni Swamp,Trinidad

Metals can have significant impacts on inhabitants of mangrove swamps as well as consumers of mangrove-associated fauna. Yet, for several Caribbean islands, assessments regarding the impact of metals on such ecosystems are particularly sparse. The present study investigated the distribution and potential impact of Cd, Cr, Cu, Ni, Pb and Zn in the Caroni Swamp, Trinidad and Tobago’s largest mangrove ecosystem. Surface sediments and mangrove oysters (Crassostrea rhizophorae) from 10 sites in the swamp were analysed for the 6 identified metals. The concentration ranges (in μg/g dry wt.) of metals in sediments from Caroni Swamp were: Zn (113.4–264.6), Cr (27–69.7), Ni (10.7–41.1) and Cu (11–40.7). Based on Canadian Sediment Quality Guidelines (CSQGs), metals in sediments posed a low to medium risk to aquatic life. The concentration ranges (in μg/g wet wt.) for metals in Crassostrea rhizophorae tissues were: Zn (123.2–660), Cu (4.2–12.3), Ni (0.1–5.5), Pb (0.1–0.9), Cr (0.2–0.3) and Cd (0.1–0.2). Multiple evaluations indicated that zinc posed a potential threat to the health of oyster consumers. Information from this study is vital for managing the Caroni Swamp, safeguarding the health of consumers of shellfish on this Caribbean island and serving as a useful baseline for future local and regional risk assessments.     

Metal binding in soil cores and sediments in the vicinity of a dammed agricultural and industrial watershed

The environment is witnessing a downgrade caused by the amelioration of the industrial and agricultural sectors, namely, soil and sediment compartments. For those reasons, a comparative study was done between soil cores and sediments taken from two locations in the Qaraaoun reservoir, Lebanon. The soil cores were partitioned into several layers. Each layer was analyzed for several physicochemical parameters, such as functional groups, particle size distribution, ζ-potential, texture, pH, electric conductivity, total dissolved solids, organic matter, cation exchange capacity, active and total calcareous, available sodium and potassium, and metal content (cadmium, copper, and lead). The metal content of each site was linked to soil composition and characteristics. The two sites showed distinguishable characteristics for features such as organic matter, pH, mineral fraction, calcareous, and metal content. The samples taken toward the south site (Q1), though contain lower organic matter than the other but are more calcareous, showed higher metal content in comparison to the other site (Q2) (average metal content of Q1 > Q2; for Cd 3.8?>?1.8 mg/kg, Cu 28.6?>?21.9 mg/kg, Pb 26.7?>?19 mg/kg). However, the metal content in this study did not correlate as much to the organic matter; rather, it was influenced by the location of the samples with respect to the dam, the reservoir’s hydrodynamics, the calcareous nature of the soil, and the variation of the industrial and agricultural influence on each site.     

Fluoride distribution and the effect of some ions along Alexandria coastal Mediterranean seawater of Egypt

The coastal seawater of Mediterranean of Alexandria receives large amount of discharged waters containing industrial wastes, sewage, and agricultural and domestic drainage. Fluoride and some parameters were( chemical and physical) determined. The data gave indication that the content and the amount of the discharged water largely affect the chemical composition of the coastal water. Stepwise regression analysis was highly significant and the model was very fruitful, where the observed and calculated values were mostly concordant. This may indicated that there was a relation between fluoride content in cosslal seawater and its content in the discharged water.     

On-line CO, CO2 emissions evaluation and (benzene, toluene, xylene) determination from experimental burn of tropical biomass

Atmospheric pollution and global warming issues are increasingly becoming major environmental concerns. Fire is one of the significant sources of pollutant gases released into the atmosphere; and tropical biomass fires, which are of particular interest in this study, contribute greatly to the global budget of CO and CO₂. This pioneer research simulates the natural biomass burning strategy in Malaysia using an experimental burning facility. The investigation was conducted on the emissions (CO₂, CO, and Benzene, Toluene, Ethylbenzene, Xylenes (BTEX)) from ten tropical biomass species. The selected species represent the major tropical forests that are frequently subjected to dry forest fire incidents. An experimental burning facility equipped with an on-line gas analyzer was employed to determine the burning emissions. The major emission factors were found to vary among the species, and the specific results were as follows. The moisture content of a particular biomass greatly influenced its emission pattern. The smoke analysis results revealed the existence of BTEX, which were sampled from a combustion chamber by enrichment traps aided with a universal gas sampler. The BTEX were determined by organic solvent extraction followed by GC/MS quantification, the results of which suggested that the biomass burning emission factor contributed significant amounts of benzene, toluene, and m,p-xylene. The modified combustion efficiency (MCE) changed in response to changes in the sample moisture content. Therefore, this study concluded that the emission of some pollutants mainly depends on the burning phase and sample moisture content of the biomass.