The concentrations, profiles, sources and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) were determined in 40 surface soil samples collected from Beijing, Tianjin and surrounding areas, North China in 2007, and all sampling sites were far from industrial areas, roadsides and other pollution sources, and across a range of soil types in remote, rural villages and urban areas. The total concentrations of 16 PAHs ranged from 31.6 to 1475.0 ng/g, with an arithmetic average of 336.4 ng/g. The highest PAH concentrations were measured in urban soils, followed by rural village soils and soils from remote locations. The remote-rural village-urban PAH concentration gradient was related to population density, gross domestic product (GDP), long-range atmospheric transport and different types of land use. In addition, the PAH concentration was well correlated with the total organic carbon (TOC) concentration of the soil. The PAH profile suggested that coal combustion and biomass burning were primary PAH sources.

In urban cities in Southern China, the tissue S/N ratios of epilithic mosses (Haplocladium microphyllum), varied widely from 0.11 to 0.19, are strongly related to some atmospheric chemical parameters (e.g. rainwater SO42−/NH4+ ratios, each people SO2 emission). If tissue S/N ratios in the healthy moss species tend to maintain a constant ratio of 0.15 in unpolluted area, our study cities can be divided into two classes: class I (S/N > 0.15, S excess) and class II (S/N < 0.15, N excess), possibly indicative of stronger industrial activity and higher density of population, respectively. Mosses in all these cities obtained S and N from rainwater at a similar ratio. Sulphur and N isotope ratios in mosses are found significantly linearly correlated with local coal δ34S and NH4+–N wet deposition, respectively, indicating that local coal and animal NH3 are the major atmospheric S and N sources.

Batch adsorption experiments were carried out to study the adsorptive removal and diffusion mechanism of para-chlorophenol (p-CP) onto Calgon Filtrasorb 400 (F400) activated carbon. The external mass transfer resistance is negligible in the adsorption process carried out under different conditions in batch operation. Intraparticle diffusion model plots were used to correlate the batch p-CP adsorption data; three distinct linear sections were obtained for every batch operation. The textural properties of F400 activated carbon showed that it has a large portion of supermicropores, which is comparable to the size of the p-CP molecules. Due to the stronger interactions between p-CP molecules and F400 micropores, p-CP molecules predominantly diffused and occupied active sites in micropore region by hopping mechanism, and eventually followed by a slow filling of mesopores and micropores. This hypothesis is proven by the excellent agreement of the intraparticle diffusion model plots and the textural properties of F400 activated carbon.

Two peat bogs from remote alpine sites in Australia were found to contain detailed and coherent histories of atmospheric metal pollution for Pb, Zn, Cu, Mo, Ag, As, Cd, Sb, Zn, In, Cr, Ni, Tl and V. Dramatic increases in metal deposition in the post-1850 AD portion of the cores coincide with the onset of mining in Australia. Using both Pb isotopes and metals, pollutants were ascribed to the main atmospheric pollution emitting sources in Australia, namely mining and smelting, coal combustion and agriculture. Results imply mining and metal production are the major source of atmospheric metal pollution, although coal combustion may account for up to 30% of metal pollutants. A novel finding of this study is the increase in the otherwise near-constant Y/Ho ratio after 1900 AD. We link this change to widespread and increased application of marine phosphate fertiliser in Australia's main agricultural area (the Murray Darling Basin).

Mt. Gongga area in southwest China was impacted by Hg emissions from industrial activities and coal combustion, and annual means of atmospheric TGM and PHg concentrations at a regional background station were 3.98 ng m-3 and 30.7 pg m-3, respectively. This work presents a mass balance study of Hg in an upland forest in this area. Atmospheric deposition was highly elevated in the study area, with the annual mean THg deposition flux of 92.5 μg m-2 yr-1. Total deposition was dominated by dry deposition (71.8%), and wet deposition accounted for the remaining 28.2%. Forest was a large pool of atmospheric Hg, and nearly 76% of the atmospheric input was stored in forest soil. Volatilization and stream outflow were identified as the two major pathways for THg losses from the forest, which yielded mean output fluxes of 14.0 and 8.6 μg m-2 yr-1, respectively.

The temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was examined in dated sediments from five lakes in Western China. The surficial concentrations of seven carcinogenic PAHs (BaA, Chyr, BbF, BkF, BaP, DBA and INP, hereafter denoted as PAH7) were highly site-specific. The ΣPAH7 concentrations generally increased from the deep layers to surface sediments. The temporal trends of ΣPAH7 concentrations were clearly different from those reported in developed countries. From 1950s to 1980s, which PAHs started to decrease in developed countries, is the right period that PAHs started to increase rapidly in Western China. The fluxes and mass inventories suggest that the PAH7 input over the past three decades was much more rapidly than it was before the 1980s. Source identification indicates that the PAHs were primarily from biomass burning and domestic coal combustion, and increasing vehicular and/or industrial coal combustion emission was also found.

Samples of airborne particulate matter (PM₂.₅) were collected at a site in Lahore, Pakistan from November 2005 to January 2006. A total of 129 samples were collected using an Andersen Reference Ambient Air Sampler 2.5-400 sampler and analyzed for major ions, trace metals, and organic and elemental carbon concentrations. The data set was then analyzed by positive matrix factorization (PMF) to identify the possible sources of the atmospheric PM collected in this urban area. Six factors reproduced the PM₂.₅ sample compositions with meaningful physical interpretation of the resolved factors. The sources included secondary PM, diesel emissions, biomass burning, coal combustion, two-stroke vehicle exhaust, and industrial sources. Diesel and two-stroke vehicles contributed about 36%, biomass burning about 15%, and coal combustion sources around 13% of the PM₂.₅ mass. Nearly two thirds of the PM₂.₅ mass is carbonaceous material. Secondary particles contributed about 30% of PM₂.₅ mass. The conditional probability function (CPF) was then used to help identify likely locations of the sources present in this area. CPF analysis point to the east and northeast, which are directions of urban and industrial areas located across the border near Amritsar, India as the most probable source for high PM₂.₅ concentration from diesel and two-stroke vehicles exhaust in Lahore. Analysis of those days within three different ranges of PM₂.₅ concentration shows that most of the measured high PM₂.₅ mass concentrations were driven by diesel and two-stroke vehicle emissions including the associated primary sulfate. The use of the potential source contribution function (PSCF) to find the source locations of regionally transported particles is inapplicable in situations when high PM₂.₅ concentrations are dominated by local sources and local meteorology.

Linear anionic polyacrylamide (LA-PAM) is being considered as a soil amendment to reduce seepage and infiltration in unlined earthen canals. While polyacrylamides have been extensively used for potable water treatment, dewatering sewage sludge, coal and mine processing, paper manufacturing, and agriculture, little is known about its ecological impact to aquatic ecosystems. Acute toxicity (LC₅₀, 24 and 48 h) and chronic exposure tests (limited and continuous exposures) were conducted on Daphnia magna. In the chronic limited exposure experiments, Daphnia were exposed to LA-PAM for only 24 h whereas for the chronic continuous exposure the concentrations of 0, 0.5, 1, 5, 10, and 100 mg/L were tested and the endpoints of growth, onset to reproduction, fecundity, and mortality were measured for the duration of 32 days. There was no significant difference among the chronic, limitedly exposed organisms. The acute toxicity for LA-PAM was measured at 100, 150, 200, 250, and 300 mg/L. The acute test showed that the LC₅₀ for LA-PAM was at 152 mg/L. Overall in the chronic, continuous exposure test, D. magna was negatively impacted by LA-PAM at levels as low as 1 mg/L. Growth was reduced by 37% and 89% at 1 and 100 mg/L, respectively. Fecundity and onset to reproduction was impaired at 10 and 100 mg/L. Kinematic viscosity ranged from 0.98 cSt at 1 mg/L to 2.9 at 100 mg/L. At these levels, mechanical and physiological impairments due to the viscous properties of LA-PAM are the proposed mechanisms of reduction in the life history traits of D. magna.

A monitoring program of particulate matter was conducted at eight sampling sites in four highly industrialized cities (Shenyang, Anshan, Fushun, and Jinzhou) of Liaoning Province in Northeast China to identify the major potential sources of ambient PM₂.₅. A total of 814 PM₂.₅ and PM₂.₅₋₁₀ samples were collected between 2004 and 2005. All PM samples were collected simultaneously in four cities and analyzed gravimetrically for mass concentrations. A sum of 16 elemental species concentrations in the PM samples were determined using inductively coupled plasma atomic emission spectroscopy. Annual means of PM₂.₅ concentrations ranged from 65.0 to 222.0 μg m⁻³ in all the eight sampling sites, and the spatial and seasonal variations were discussed. Enrichment factors were calculated, and Cr, Cu, Zn, As, Cd, and Pb will be pollution-derived elements. Site-to-site comparisons of PM₂.₅ species in each city were examined using coefficient of divergence, revealing that the two sites in each city are similar in elemental species. Principle component analysis was used for preliminary source analysis of PM₂.₅. Three or four factors in each city were isolated, and similar sources (crustal source, coal combustion, vehicle exhaust, iron making, or some other metallurgical activities) were identified at four cities.

We assessed the impacts of a specific conductance gradient attributable to treated coal-mining discharges on the fish communities of a southwestern Pennsylvania stream. Total dissolved solids concentrations were determined from specific conductance values. A total of 10,940 fish representing seven families and 42 species/hybrids were collected from 17 stations over the entire survey. Species richness, density, and the coefficient of community loss (I) showed marked impairment at the two stations directly below the discharges and the downstream recovery was interrupted at one station by untreated discharges from a mine refuse pile. Species richness declined from 28 at the reference site to 7 at the station directly below the treated effluents. This study suggests that the threshold for in-stream conductivity impairment to fish communities in this region is in the range of 3,000-3,500 µS/cm and 2,000-2,300 mg/l of total dissolved solids, respectively.