Historical trends in trace element deposition were analyzed using herbaria specimens. We determined Al, Fe, Mg, Mn, Ca, Na, P, K, S, As, Cd, Cr, Cu, Ni, Pb and Zn contents in leaves of eight specimens collected in 1941. To assess changes, we collected the same plants from a botanical garden in 2012. The concentrations of major elements showed large species variability. However, temporal trends were predominately detected for heavy metals. The Cd, Ni and Cr contents in the 2012 leaves were 10, 13 and 16 times higher, respectively, than in 1941. Urban activities have substantially raised the levels of these metals in urban atmospheres due to changes in human activities over 70 years of urban growth. Nevertheless, Pb has decreased (−126%) in recent decades thanks to controlled lead fuel combustion. In short, metal deposition trend to increase Cr, Ni and Cd levels.

This study aims to investigate factors leading to agglomeration of citrate coated silver (AgNP-Cit), polyvinylpyrrolidone coated AgNPPVP and titanium dioxide (TiO2) nanoparticles in surface waters and wastewater. ENPs (1 mg/L) were spiked to unfiltered, filtered, ultrafiltered (<10 kDa and <1 kDa) samples. Z-average particle sizes were measured after 1 h, 1 day and 1 week. AgNP-PVP was stable in all fractions of the samples and kept their original size around 60 nm over 1 week. Agglomeration of AgNP-Cit and TiO2 was positively correlated with Ca2+ concentration, but dissolved organic carbon concentrations > 2 mg/L contributed to stabilizing these NP. Moreover, agglomeration of AgNP-Cit in the various organic matter fractions showed that high molecular weight organic compounds such as biopolymers provide stabilization in natural water. A generalized scheme for the agglomeration behavior of AgNP-Cit, AgNP-PVP and TiO2 in natural waters was proposed based on their relation with Ca2+, Mg2+ and DOC concentration.

Atmospheric deposition in the Athabasca Oil Sands Region decreased exponentially with distance from the industrial center. Throughfall deposition (kg ha−1 yr−1) of NH4–N (.8–14.7) was double that of NO3–N (.3–6.7), while SO4–S ranged from 2.5 to 23.7. Gaseous pollutants (NO2, HNO3, NH3, SO2) are important drivers of atmospheric deposition but weak correlations between gaseous pollutants and deposition suggest that particulate deposition is also important. The deposition (eq ha−1) of base cations (Ca + Mg + Na) across the sampling network was highly similar to N + S deposition, suggesting that acidic deposition is neutralized by base cation deposition and that eutrophication impacts from excess N may be of greater concern than acidification. Emissions from a large forest fire in summer 2011 were most prominently reflected in increased concentrations of HNO3 and throughfall deposition of SO4–S at some sites. Deposition of NO3–N also increased as did NH4–N deposition to a lesser degree.

We synthesized the effects of ozone on wheat quality based on 42 experiments performed in Asia, Europe and North America. Data were analysed using meta-analysis and by deriving response functions between observed effects and daytime ozone concentration. There was a strong negative effect on 1000-grain weight and weaker but significant negative effects on starch concentration and volume weight. For protein and several nutritionally important minerals (K, Mg, Ca, P, Zn, Mn, Cu) concentration was significantly increased, but yields were significantly decreased by ozone. For other minerals (Fe, S, Na) effects were not significant or results inconclusive. The concentration and yield of potentially toxic Cd were negatively affected by ozone. Some baking properties (Zeleny value, Hagberg falling number) were positively influenced by ozone. Effects were similar in different exposure systems and for spring and winter wheat. Ozone effects on quality should be considered in future assessments of food security/safety.

A series of experiments were performed to simulate the environmental behavior and fate of graphene oxide nanoparticles (GONPs) involved in the surface environment relating to divalent cations, natural organic matter (NOM), and hydraulics. The electrokinetic properties and hydrodynamic diameters of GONPs was systematically determined to characterize GONPs stability and the results indicated Ca2+ (Mg2+) significantly destabilized GONPs with high aggregate strength factors (SF) and fractal dimension (FD), whereas NOM decreased aggregate SF with lower FD and improved GONPs stability primarily because of increasing steric repulsion and electrostatic repulsion. Furthermore, the GONPs resuspension from the sand bed into overlying water with shear flow confirmed that the release would be restricted by Ca2+ (Mg2+), however, enhanced by NOM. The interaction energy based on Derjaguin–Landau–Verwey–Overbeek theory verifies the aggregation and resuspension well. Overall, these experiments provide an innovative look and more details to study the behavior and fate of GONPs.

The anatomical and chemical characteristics of sweetgum were studied after 11 years of elevated CO2 (544 ppm, ambient at 391 ppm) exposure. Anatomically, branch xylem cells were larger for elevated CO2 trees, and the cell wall thickness was thinner. Chemically, elevated CO2 exposure did not impact the structural components of the stem wood, but non-structural components were significantly affected. Principal component analysis (PCA) was employed to detect differences between the CO2 treatments by considering numerous structural and chemical variables, as well as tree size, and data from previously published sources (i.e., root biomass, production and turnover). The PCA results indicated a clear separation between trees exposed to ambient and elevated CO2 conditions. Correlation loadings plots of the PCA revealed that stem structural components, ash, Ca, Mg, total phenolics, root biomass, production and turnover were the major responses that contribute to the separation between the elevated and ambient CO2 treated trees.

A Terrestrial Biotic Ligand Model (TBLM) for Ni toxicity to barley root elongation (RE) developed from experiments conducted in sand culture was used to predict toxicity in non-calcareous soils. Ca2+ and Mg2+ concentrations and pH in sand solution were varied individually and TBLM parameters were computed. EC50 increased as Mg2+ increased, whereas the effect of Ca2+ was insignificant. TBLM parameters developed from sand culture were validated by toxicity tests in eight Ni-amended, non-calcareous soils. Additional to Ni2+ toxicity, toxicity from all solution ions was modelled independently as an osmotic effect and needed to be included for soil culture results. The EC50s and EC10s in soil culture were predicted within twofold of measured results. These are close to the results obtained using parameters estimated from the soil culture data itself.

Metals bioaccumulated in aquatic organisms are considered to be a good indicator of bioavailable metal contamination levels in freshwaters. However, bioaccumulation depends on the metal, the species, and the water chemistry that influences metal bioavailability. In the laboratory, a kinetic model was used to describe waterborne Pb bioaccumulated in Gammarus pulex. Uptake and elimination rate constants were successfully determined and the effect of Ca2+ on Pb uptake was integrated into the model. Thereafter, accumulated Pb concentrations in organisms were predicted with the model and compared with those measured in native populations from the Seine watershed (France). The predictions had a good agreement with the bioaccumulation levels observed in native gammarids and particularly when the effect of calcium was considered. To conclude, kinetic parameters experimentally derived for Pb in G. pulex are applicable in environmental conditions. Moreover, the consideration of the water's chemistry is crucial for a reliable interpretation of bioaccumulation.

The Clinch and Powell Rivers (Virginia, USA) support diverse mussel assemblages. Extensive coal mining occurs in both watersheds. In large reaches of both rivers, major ion concentrations are elevated and mussels have been extirpated or are declining. We conducted a laboratory study to assess major ion effects on growth and survival of juvenile Villosa iris. Mussels were exposed to pond water and diluted pond water with environmentally relevant major ion mixtures for 55 days. Two treatments were tested to mimic low-flow concentrations of Ca2+, Mg2+, SO42−, HCO3+, K+ and Cl− in the Clinch and Powell Rivers, total ion concentrations of 419 mg/L and 942 mg/L, respectively. Mussel survival (>90%) and growth in the two treatments showed little variation, and were not significantly different than in diluted pond water (control). Results suggest that major ion chronic toxicity is not the primary cause for mussel declines in the Clinch and Powell Rivers.

Particulate matter samples were collected from several locations during September 2011 and September 2012 in Riyadh, Saudi Arabia. In addition to determining particulate matter (as PM10) concentrations, the samples were analyzed for several metals and ions. PM concentration was approximately 3 times higher than the Country’s ambient air quality standards respectively. Metals and ions contributed to about 21.5% and 16.2% of the PM concentrations respectively. Summer vs. winter comparison showed that PM concentrations were approximately 84% higher in summer and the crustal matter species such as Fe, Mn, Ti, Ca+2, Mg+2 increased several folds in summer, primarily attributed to dust storms. The weekdays PM concentrations were 17% more than the weekend concentrations, indicating weekday activities contribute to the concentrations. The dust storms lead to over 200% increase in the PM and some elements primarily Al, Fe, Mg and Ca. Spatial comparison at industrial and residential locations revealed about 60% increase in PM concentrations and substantial increase in Zn, Mn, B, Mg, Fe, and Al and the ions K+, SO4--, and Cl- at industrial locations. Bivariate correlations among the metals and ions demonstrated that strong correlation existed between Al, Fe, Mg, K and Mn suggesting a common origin for these species i.e. the crustal mineral aerosols. The correlations among cations and anions implied the presence of compounds in the atmosphere such as CaSO4, (NH4)2SO4, KCl, KSO4, and also to some extent MgSO4. An investigation of ionic ratios revealed that ratios SO4-2/NO3-, Ca+2/K+, and Ca+2/Na+ could be possible indicators to identify scenarios industrial over residential locations, storm days over no storm days and summer over winter periods respectively.