The aim of our study was to investigate how exposure to heavy metal-rich waters from gypsum mining affects the morphology and levels of primary DNA damage in Gammarus balcanicus. Chemical analysis revealed increased concentrations of metals in water and sediment collected at a site impacted by gypsum mine wastewaters. The specimens also showed elevated total tissue metal levels when compared with the organisms collected at the reference site. The most prominent increase was observed for strontium, followed by iron, nickel, vanadium, aluminium, and manganese. The major pathway of entry for these toxic substances was through the degraded exoskeleton as a consequence of excessive strontium input (unbalanced calcium/strontium ratio) and altered permeability. Disturbed exoskeleton integrity was observed only in individuals collected downstream of the gypsum mine, which was confirmed by electron microscopy. Levels of primary DNA damage were evaluated using the alkaline comet assay in the haemolymph of the specimens.

Protons and other cations may inhibit metal uptake and alleviate metal toxicity in aquatic organisms, but less is known about these interactions in soil organisms. The present study investigated the influence of solution chemistry on uptake and toxicity of Ni in Enchytraeus crypticus after 14 days exposure. Ca2+, Mg2+ and Na+ were found to exert significant effects on both uptake and toxicity of Ni. An extended Langmuir model, which incorporated cation competition effects, well predicted Ni uptake. The LC50{Ni2+} predicted by a developed Biotic Ligand Model matched well with observed values. These suggest that cation competition needs to be taken into account when modelling uptake and effects. The binding constants of Ni2+, Mg2+ and Na+ on the uptake and toxic action sites were similar, but for Ca2+ they differed. This indicates that the effect of Ca2+ on Ni2+ toxicity cannot simply be explained by the competition for entry into organism.

This study aims to investigate effects of freshwater components in order to predict agglomeration behavior of silver nanoparticles coated with citrate (AgNP-Cit), polyvinylpyrrolidone (AgNP-PVP), and of TiO2 nanoparticles. Agglomeration studies were conducted in various media based on combinations of ions, natural organic matter (humic, fulvic acid) and surfactants (sodium dodecyl sulfate, alkyl ethoxylate), at a constant ionic strength of 10 mM over time for up to 1 week. Agglomeration level of AgNP-Cit and TiO2 was mostly dependent on the concentration of Ca2+ in media, and their size strongly increased to micrometer scale over 1 week. However, AgNP-Cit and TiO2 were stabilized to particle size around 500 nm in the presence of NOM, surfactants and carbonate over 1 week. AgNP-PVP maintained their original size in all media except in the presence of Mg2+ ions which led to significant agglomeration. Behavior of these engineered nanoparticles was similar in a natural freshwater medium.

Studying the physiologic effects of components of fine particulate mass (PM2.5) could contribute to a better understanding of the nature of toxicity of air pollution.We examined the relation between acute changes in cardiovascular and respiratory function, and PM2.5-associated-metals.Using generalized linear mixed models, daily changes in ambient PM2.5-associated metals were compared to daily changes in physiologic measures in 59 healthy subjects who spent 5-days near a steel plant and 5-days on a college campus.Interquartile increases in calcium, cadmium, lead, strontium, tin, vanadium and zinc were associated with statistically significant increases in heart rate of 1–3 beats per minute, increases of 1–3 mmHg in blood pressure and/or lung function decreases of up to 4% for total lung capacity.Metals contained in PM2.5 were found to be associated with acute changes in cardiovascular and respiratory physiology.

Irregular discharges of polluted stormwater into drainage systems during base flow (no rainfall) result in acute ecological impacts within fluvial and estuarine environments. In this study, metal and TSS concentrations were significantly more variable during business hours of weekdays (i.e. high-business activity) than weekends/public holidays (i.e. low-business activity) within three highly-urbanised catchments of Sydney estuary (Australia), as determined by analysing multivariate dispersion (PERMDISP). Concentrations of TSS and all metals analysed (Al, Ca, Cu, Fe, Mg, Pb and Zn) were also significantly greater during high- than low-business periods within at least one of the three catchments. In no case were concentrations significantly higher during low- than high-business periods. This pattern of contamination supports the hypothesis that commercial and industrial sources are major contributors of irregular discharges of contamination to Sydney estuary. Irregular discharges and consequential ecological impacts may be effectively reduced in this environment by focussing management efforts on these activities.

No studies document essential (calcium, magnesium, phosphorus, potassium, sodium), trace (barium, boron, chromium, cobalt, copper, iron, manganese, molybdenum, selenium, zinc) or toxic element (antimony, arsenic, cadmium, lead, mercury, thallium) concentrations in any members of the family Molidae, including the world’s largest bony fish, the ocean sunfish (Mola mola). Here, we analyzed 21 elements in the liver of one M. mola. These values were compared to liver concentrations in multiple species with spatial and dietary overlap. Concentrations of calcium (3339ppm wet weight) and iron (2311ppm wet weight) were extremely elevated in comparison to a number of other fish species, indicating that calcium and/or iron toxicity may have occurred in this animal. Concentrations of toxic elements were generally low, with the exception of cadmium (3.5ppm). This study represents the first report of essential, trace and toxic elements in this species.

Marine biofouling is a serious environmental problem worldwide. As an effort to find environmental friendly antifoulants, indole derivatives were determined for their activities to inhibit the growth of bacteria and diatom. The minimum inhibitory concentrations (MICs) of indole derivatives against bacteria were very low, especially for 6-chloroindole. It was proved that 6-chloroindole obviously inhibited the growth of bacteria, interfered with the formation of bacterial biofilm, destroyed bacterial cell morphology and also inhibited the growth of diatom Cylindrotheca sp. as well. By using noninvasive micro-test technique (NMT), 6-chloroindole triggered algal cellular Ca2+ efflux. The highest value was 72.03pmolcm−2s−1, 10.6 times of the control group. The present studies indicated that indole derivatives might have the potential to be new antifouling agents because of their excellent antibacterial and anti-algal activities. At the same time, Ca2+ efflux might be one of the mechanisms that indole derivatives inhibited the growth of diatom.

The suitability of a rootless Bromeliad species (Tillandsia usneoides) as biomonitor of airborne trace elements in urban areas of the Mediterranean basin was evaluated. The study was performed at five sites of the city of Pisa (Tuscany, Central Italy) differing for land use, anthropogenic activities and/or proximity to emission sources. The elements investigated were Al, As, B, Ba, Bi, Ca, Cd, Co, Cr, Cs, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, Sb, Sr, V and Zn. Unwashed and washed samples, collected after 36 days of exposure (May–June 2011), were analyzed by ICP–MS. Results showed significant differences among sampling sites for several elements. Concentrations of Al, Ba, Bi, Cd, Co, Cu, Pb, Sb and Zn were the highest in urban/traffic and/or suburban/traffic areas. Some of these elements e.g. Ba, Cu, Sb and Zn are commonly considered as traffic–related elements. In the industrial site, the main elements found were Mg, Sr and Zn. Iron, Mn, Na and V concentrations were much higher in rural/remote areas. Enrichment factors highlighted that T. usneoides showed: high resistance/tolerance to heavy metal toxicity, specificity, capability to well–definitely represent a sampling site, quantitative response to pollutant exposure. The results indicated that T. usneoides reflects the intrinsic characteristics of each sampling area and allows tracing back differences related to the various emission sources by factor analysis.

The size distribution of water-soluble inorganic components of urban aerosols in Shanghai was studied. The size-resolved aerosol samples collected by an 8-stage cascade sampler between April and May of 2012 were analyzed by ion chromatography. The ion mass concentrations followed the sequence of SO42−>NO3−~NH4+>Ca2+>Na+ ~Cl−>K+>Mg2+>F− for each size fraction below 2.1μm, while the sequence was NO3−>SO4−2>Ca2+>NH4+>Na+>Cl−>K+>Mg2+>F− for coarse mode particles larger than 3.3μm. The size distribution in 5 fractions showed that SO42−, NO3−, and NH4+ were generally in the fine mode peaking below 1μm while Ca2+, Mg2+, Na+, and Cl− were bimodally distributed with a second peak larger than 2.1μm. Back trajectory analyses revealed that the air masses could be classified into three main groups. The total ion concentrations were comparable between the terrestrial and mixing regimes. In the terrestrial regime, fine mode sulfate and nitrate were predominantly associated with ammonium. The excessive sulfate and nitrate over the whole size range might exist in the forms of Ca(NO3)2 and CaSO4. In the maritime regime, the decrease in SO42−, NO3−, and NH4+ contributed to the improvement in air quality. Besides marine aerosols, local emissions from soil dust and coal combustion were also important sources of sea-salt type ions (i.e., Na+ and Cl−).

Urban fugitive dust samples were collected to determine the chemical profiles of fugitive dust over Xi'an. Seventy eight samples were collected and divided into categories of paved road dust, construction dust, cement dust, and soil dust. Eighteen elements, including Na, Mg, Al, Si, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Ba, and Pb, and eight water–soluble inorganic ions, including Na+, Mg2−, Ca2−, NH4−, F−, Cl−, NO3− and SO42−, were measured. The most abundant elements in these urban dust samples were Al, Si, Ca, and Fe. Al, Si, K, and Ti and showed strong positive correlations with each other, indicating they are typical dust trace elements. In contrast, elements of Ca, Zn, As, and Pb had negative correlations to crustal elements. Si/Al, K/Al, Ti/Al, Mn/Al, and Fe/Al ratios varied insignificantly among these four samples types; these ratios are similar to the properties of loess, desert, and Gobi soil dust reported in previous studies. A significantly higher Ca/Al ratio was dominant in the chemical profile of the cement samples. In addition, high Pb/Al and Zn/Al ratios were detected in comparison with those in the Gobi soil, desert soil, and loess soil samples, which indicated that Pb/Al and Zn/Al ratios can be considered as markers of urban dust. To t a l water–soluble ions occupied only a small fraction (<5%) in the urban fugitive soil samples indicating that most of the materials in the fugitive dust were insoluble. Ca2+ and SO42− were the most abundant ions in all samples. Most of the Ca and K in the fugitive soil samples were in insoluble phases, which differ significantly in comparison with combustion sources. A strong correlation was observed between Ca2+ and estimated CO32− levels indicating that most of Ca2+ was in the form of CaCO3 rather than other calcium minerals in Xi’an fugitive dust.