The concentrations of selected metals—Cr, Ni, Cu, Zn, Cd, and Pb—were determined in the samples of Hypogymnia physodes lichen and Pleurozium schreberi moss collected in Polish and Czech Euroregions Praded and Glacensis. More specifically, the samples were collected in Bory Stobrawskie, Bory Niemodlińskie, and Kotlina Kłodzka (Poland) and in Jeseniki (Czech Republic). The concentration of metals in the samples was measured using the atomic absorption spectrometry (flame AAS technique and electrothermal atomization AAS technique). The results were used to calculate the comparison factor (CF) that quantifies the difference in concentration of a given bioavailable analyte × accumulated in lichens and mosses: CF = 2 (c x,lichen − c x,moss) (c x,lichen + c x,moss)−1. The values of CF greater than 0.62 indicate the most probable location of heavy metals deposited in the considered area. In this work, the method was used to show a significant contribution of urban emissions to the deposition of heavy metals in the area of Bory Stobrawskie and in the vicinity of Kłodzko City.

This study assessed effects of a mixture of two pesticides, diazinon and permethrin, on 48-h sediment toxicity to Hyalella azteca in a constructed wetland mesocosm containing non-vegetated and vegetated sections. Sediment samples were collected at inflow, middle, and back points within each section 5, 24, 72 h, 7, 14, and 21 days post-amendment. Pesticides were detected in sediments throughout non-vegetated and vegetated wetland sections. H. azteca 48-h survival varied across sampling period, wetland location, and vegetation type with lowest survival occurring within the first 72 h of the inflow and middle locations of the non-vegetated section. Sediment toxicity was ameliorated by 14 and 7 days within the non-vegetated and vegetated sections, respectively. Relationships between pesticide concentrations and animal survival indicated toxicity was from both diazinon and cis-permethrin in the non-vegetated section and primarily cis-permethrin in the vegetated section. Results show that vegetation ameliorated pesticide mixture 48-h sediment toxicity to H. azteca earlier and to a greater extent than non-vegetated constructed wetlands. A 21-day retention time is necessary to improve 48-h H. azteca sediment survival to ≥90% in wetlands of this size.

Numerous time series studies have quantified the potential association between daily variations in air pollution and daily variations in non-accidental deaths. In order to account for the presence of unmeasured confounders, a smooth function of time trend is typically used as a proxy for these variables. We shed light on the validity of the results obtained by using this approach. Specifically, we use data from the National Morbidity, Mortality and Air Pollution Study database, and carry out a carefully designed simulation study. Our findings suggest that the use of a smooth function of time trend cannot fully account for the presence of unmeasured confounders, especially when their impact is strong relatively to the effect of air pollution, and when several unobservables are not included in the model.

In this study, the effects of industrial and urban pollution on Pb, Al, Cd, Cu, and Zn accumulation, peroxidase activity, and pigment and protein contents were investigated in shrub and tree leaves in Antakya, Turkey. We determined that industrial and traffic activities produce the most plant-incorporated air pollutants in Antakya City. Cu and Al amounts were high in plants in the urban street location and Cd, Pb, and Zn amounts where high for all plants in the industrial site. Acer negundo L. showed maximum Pb and Zn accumulation at the industrial site and Al accumulation for the urban street site. Higher Cd and Cu amounts were detected in Platanus orientalis L. and Nerium oleander L. in the industrial and urban street sites, respectively. Compared to the control site, decreases in pigment and total soluble protein contents and increases in peroxidase enzyme activity were more evident in industrial and urban street sites. Our results indicated that industry and urban air pollution is high in Antakya City and Pb pollution was at an especially alarming level for vegetation and human health.

Aqueous natural organic matter (NOM) impacted by two contrasting human impacts was analyzed using by multiresponse fluorescence, decoupled with the resolution routine PARAFAC. The first site is Chalk River, Ontario, Canada, near a pit formerly used to dispose low-level wastes. The second site is the Grand River in Cambridge, south-central Ontario, which is impacted by urban activities and agriculture. Our analysis included raw water, plus fractions from ultrafiltration and solid-phase extraction (SPE). The fluorescence spectra of the NOM, resolved with PARAFAC, showed three common features: humic-like components, at excitation/emission wavelengths 325-350/450-475 nm, fulvic-like components at 325/380-420 nm and protein-like components, at 275/300 nm. Ultrafiltration revealed that most of the NOM comprised fine material below 5,000 Da cut-off (<4% of the total) in the urban-impacted sites and the clean site at Chalk River, but the colloidal fraction (larger than 5,000 Da) was substantially higher in the contaminated water, with ∼18-26% of the total. The protein-like components in the contaminated Chalk River water were affected by ultrafiltration, but less so in the clean Chalk River sample and the urban-impacted waters. SPE preferentially removed the protein-like component in the contaminated Chalk River water (typically 89-95% signal decrease), but had a limited effect on humic- and fulvic-like components elsewhere. In conclusion, multiresponse fluorescence provided new information on the NOM quality from two contrasting sites, aided by ultrafiltration and SPE. These results are consistent with the in situ production of NOM in the Chalk River contaminated site, and natural production at the other sites.

This study examined the relationship between abundance of submerged aquatic vegetation (SAV) and the water trophic status of a group of lakes located in northwestern Hillsborough county. SAV abundance was expressed by the percent of lake volume infested with SAV (PVI) and the percent of lake area covered with SAV (PAC). The group of lakes was divided into two subgroups based on SAV abundance less than 20 PVI (PVI < 20) and lakes with more than 20 PVI (PVI > 20). Mean concentrations of total phosphorus (TP), total nitrogen (TN), and chlorophyll-α in lake water were used as indicators of trophic status, with the concentration of each nutrient in one group of lakes compared to its corresponding concentration in the other group. Lakes with PVI < 20 had a mean concentration of TP and chlorophyll-α of 28 and 11 µg/l, respectively, while those with a PVI > 20 had a mean concentration of 18 and 4 µg/l for the same parameters, respectively. The results of a t test and one-way ANOVA performed at the 95% confidence level indicated that the differences were significant for the concentrations of TP and chlorophyll-α but not for TN, the last of which had a mean lake water concentration of 0.8 and 0.7 mg/l for the PVI < 20 and PVI > 20 subgroups, respectively.

Reducing conditions of submerged soils were simulated in laboratory experiments by keeping various soil samples from urban areas under an aqueous solution in sealed flasks for several lengths of time. A polluted soil from a different origin was also included for comparison. Metals dissolved at various times were determined, and availability and bio-accessibility of metals present in the solid phase were estimated. Although significant amounts of Fe and Mn were dissolved, other metals were released to the solution to a much lesser extent. This effect is attributed to the greater solubility of reduced forms of Fe and Mn, and the small amounts of other metals dissolved during water-logging were related with metals retained by, or occluded in, the reduced Fe or Mn compounds. The amounts of available and bio-accessible metals remaining in the solid phase were significantly increased by water-logging, particularly the latter form. Such increase of metal mobility is likely to favour metal leaching to the water table as well as the transfer of potentially toxic elements to humans during recreational activities.

In this paper, two Indian fly ashes (from Talcher and Ramagundam) were converted into zeolites and both the raw fly ash and zeolite were used to treat two British acidic mine waters. The results demonstrate that fly ash zeolites are more effective than raw fly ash for treatment of acid mine drainage. Fly ash has been found effective for removal of Pb, but with increased dosing, caused release of Ba, Cr, Sr (both fly ashes) plus Zn, Ni (Talcher), or Fe (Ramagundam) into mine water. In contrast, increased dosing with fly ash zeolite removed 100% Pb, 98.9% Cd, 98.8% Zn, 85.6% Cu, 82.8% Fe, 48.3% Ni, and 44.8% Ba from mine water. Fly ash is amorphous in nature and many metals attached on the surface of the ash particles are easily leached off when ash comes in contact with acidic mine water. However, fly ash zeolite is crystalline in nature and due to its high cation exchange properties, most of the metals present in acid mine water are retained in surface sites.

Neutral starch microspheres (NSMs) were synthesized with epichlorohydrin as the cross-linking agent from soluble starch by inverse microemulsion method. Anionic starch microspheres (ASMs) were prepared from NSMs by the secondary polymerization with chloroacetic acid as the anionic etherifying agent. Scanning electron microscopy (SEM) revealed that microspheres had good sphericity and fine dispersibility, and the average particle size was about 75 μm. The adsorption procedure of Cu2+, Pb2+ on ASMs was carried out by batch experiments, Langmuir and Freundlich adsorption models were applied to describe the experimental isotherms, the adsorption equilibrium data were found to fit the Langmuir and Freundlich isotherm model, the Freundlich isotherm was more adequate than the Langmuir isotherm in simulating the adsorption isotherm of Cu2+,the adsorption of Cu2+, Pb2+ on ASMs was a spontaneous, the isosteric heat of adsorption at different adsorption levels was always negative and indicative of an exothermic process. The pseudo first- and second-order kinetic models were used to describe the kinetic data, and the rate constants were evaluated. The experimental data fitted well to the second-order kinetic model, which indicated that the chemical sorption was the rate-limiting step, instead of mass transfer.

The Diep River is a major freshwater ecosystem in the Western Cape, South Africa. Although it is surrounded by many sources of metal pollution, the actual metal levels in this river system are unknown. Wetland plants are known to accumulate metals and may possibly be used as biomonitors of metal contamination in a river system. One such species, the sedge Bolboschoenus maritimus, is found in abundance along the banks of this river. The aim of this study was to investigate and monitor the degree of metal contamination in the water and sediments of the lower Diep River, as well as to study the seasonal accumulation and distribution of metals in B. maritimus, and the use thereof as biomonitor species. Two sampling sites were used: one site above the wetland section of the river, receiving runoff mainly from agricultural lands (site 1), and one site close to the river mouth (site 2), exposed to several possible pollution sources. Water, sediment, and plant (root, leaf and stem) samples were collected seasonally for 1 year and analyzed for Al, Zn, Cu, and Fe. There was greater bioaccumulation of metals by plants at site 2, due to greater bioavailability of metals. B. maritimus was shown to be a root accumulator of metals. Seasonal fluctuations in root, stem, and leaf metal concentrations did not follow seasonal sediment concentration patterns. However, using B. maritimus as test species did provide valuable additional information to sediment and water analyses. More extensive research is needed to conclude whether this species is an effective biomonitor in the lower Diep River environment.