There are limited data on persistent organic pollutants (POPs) in the soils of the Tibetan Plateau. This paper presents data from a survey of organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in 40 background surface (0–5 cm) soils of the Tibetan Plateau. Soil concentrations (pg/g, dw) ranged as follows: DDTs, 13-7700; HCHs, 64-847; HCB, 24-564; sum of 15 PCBs, 75-1021; and sum of 9 PBDEs, below detection limit −27. Soil DDT, HCB, PCB and PBDE concentrations were strongly influenced by soil organic carbon content. HCH concentrations were clearly associated with the proximity to source regions in south Asia. The air–soil equilibrium status of POPs suggested the Tibetan soils may be partial “secondary sources” of HCB, low molecular weight PCBs and HCHs and will likely continue to be “sinks” for the less volatile DDE and DDT.

Several recent studies have reported temporal trends in metal contamination in mosses, but such assessments did not evaluate uncertainty in temporal changes, therefore providing weak statistical support for time comparisons. Furthermore, levels of contaminants in the environment change in both space and time, requiring space-time modelling methods for map estimation. We propose an indicator of spatial and temporal variation based on space-time estimation by indicator kriging, where uncertainty at each location is estimated from the local distribution function, thereby calculating variability intervals for comparison between several biomonitoring dates. This approach was exemplified using copper concentrations in mosses from four Portuguese surveys (1992, 1997, 2002 and 2006). Using this approach, we identified a general decrease in copper contamination, but spatial patterns were not uniform, and from the uncertainty intervals, changes could not be considered significant in the majority of the study area.

Mercury loads in tropical estuaries are largely controlled by the rainfall regime that may cause biodilution due to increased amounts of organic matter (both live and non-living) in the system. Top predators, as Trichiurus lepturus, reflect the changing mercury bioavailability situations in their muscle tissues. In this work two variables [fish weight (g) and monthly total rainfall (mm)] are presented as being important predictors of total mercury concentration (T-Hg) in fish muscle. These important explanatory variables were identified by a Weibull Regression model, which best fit the dataset. A predictive model using readily available variables as rainfall is important, and can be applied for human and ecological health assessments and decisions. The main contribution will be to further protect vulnerable groups as pregnant women and children. Nature conservation directives could also improve by considering monitoring sample designs that include this hypothesis, helping to establish complete and detailed mercury contamination scenarios.

Psychotropic substances were monitored in eight big cities of Italy over one year, starting in May 2010, in the frame of the Ariadrugs Project. Yearly average concentrations ranged from 0.02 ± 0.01 to 0.26 ± 0.11 ng/m³ for cocaine, from 0.05 ± 0.05 to 0.96 ± 1.37 ng/m³ for cannabinoids, from 16 ± 6 to 61 ± 28 ng/m³ for nicotine, and from 1.0 ± 0.8 to 8 ± 7 ng/m³ for caffeine. Palermo and Turin were the cities suffering the lowest and the highest psychotropic substance concentrations, respectively. Nicotine and cocaine exhibited trends less seasonally modulated than common air toxicants. Caffeine and cannabinoids peaked in winter dropping close to zero from May to August. In Rome, where various anthropic contours were investigated in February 2011, differences were observed both in net concentrations and ratios of psychotropic substances vs. regulated toxicants. Ambient drugs look as a consequence of addiction and their burdens give insights about the corresponding consumes.

To investigate the bioaccumulation patterns of microcystins (MCs) in organs of two gastropods, samples were collected in Lake Dianchi monthly from May to October, 2008, when cyanobacteria typically bloom. The average MCs concentrations for Radix swinhoei (pulmonate) and Margarya melanioides (prosobranch) tended to be similar for the different organs: the highest values in the hepatopancreas (9.33 by 3.74μg/g DW), followed by digestive tracts (1.66 by 3.03μg/g DW), gonads (0.45 by 1.34μg/g DW) and muscles (0.22 by 0.40μg/g DW). Pulmonate had higher value than prosobranch because of the stronger bioaccumulation ability in hepatopancreas. The levels in organs of R. swinhoei were correlated with environmentally dissolved MCs, but influenced by intracellular MCs for M. melanioides. The estimated MCs concentrations in edible parts of M. melanioides were beyond the WHO’s provisional tolerable daily intake (0.04μg/kg), suggesting the risk of consumption of M. melanioides from the lake.

Annual and weekly mercury (Hg) concentrations, precipitation depths, and Hg wet deposition in the Great Lakes region were analyzed by using data from 5 monitoring networks in the USA and Canada for a 2002–2008 study period. High-resolution maps of calculated annual data, 7-year mean data, and net interannual change for the study period were prepared to assess spatial patterns. Areas with 7-year mean annual Hg concentrations higher than the 12 ng per liter water-quality criterion were mapped in 4 states. Temporal trends in measured weekly data were determined statistically. Monitoring sites with significant 7-year trends in weekly Hg wet deposition were spatially separated and were not sites with trends in weekly Hg concentration. During 2002–2008, Hg wet deposition was found to be unchanged in the Great Lakes region and its subregions. Any small decreases in Hg concentration apparently were offset by increases in precipitation.

Methylmercury (MeHg), dissolved organic carbon (DOC), and sulfate (SO₄ ⁼) relationships were investigated in the mining-influenced St. Louis River watershed in northeast Minnesota. Fewer wetlands and higher SO₄ ⁼ in the mining region lead to generally lower availability and solubility of DOC in mining streams compared to non-mining streams. MeHg concentrations, however, are similarly low in mining and non-mining streams during low flow periods, implying that the extra DOC found in non-mining streams carries little MeHg with it during these periods. High water levels elevated MeHg concentrations in both stream types owing to release from wetlands of DOC species that contain MeHg and remain relatively soluble in streams with elevated ionic strength. In-river methylation appeared to be a negligible component of the MeHg budget for the St. Louis River during this study as MeHg and DOC concentrations were intermediate to those observed in its mining-influenced and wetland-dominated tributaries.

Transfer of aqueous methylmercury (MeHg) to primary consumers in aquatic foodwebs is poorly understood despite its importance for bioaccumulation of MeHg. We studied bioaccumulation of MeHg in simple aquatic food chains of two humic boreal streams in relation to streamwater chemistry, food web characteristics and dietary fatty acid (FA) biomarkers. Transfer of aqueous MeHg into primary consumers was similar in both streams, resulting in higher MeHg in consumers in the MeHg-rich stream. Trophic enrichment of MeHg and dietary retention of FA biomarkers was the same in both streams, suggesting that exposure to aqueous MeHg at the base of the food chain determined levels of MeHg in biota. In addition, contents of dietary biomarkers suggested that ingestion of algae reduced MeHg bioaccumulation, while ingestion of bacteria stimulated MeHg uptake. Dietary uptake of bacteria could thus be an important pathway for MeHg-transfer at the bottom of food chains in humic streams.

∑₃₀PAH gas phase concentrations (13–86 and 22–40 ng m⁻³ in the Mediterranean and Black Seas, respectively) dominated the atmospheric levels due to the high contribution of phenanthrene, dibenzothiophene and their alkylated derivates. The high variability of PAH atmospheric concentrations in the different sub-basins is due to several factors (i.e. air-mass trajectory, proximity to sources and losses by deposition). The ∑₃₀PAH atmospheric deposition (dominated by low MW PAH net air–water diffusive fluxes) is estimated to be ∼3100 ton y⁻¹ (Mediterranean) and ∼500 ton y⁻¹ (Black Sea). Net volatilization for certain PAHs was estimated. Deposition fluxes (1–2 orders of magnitude higher than reported PAH settling fluxes in the water column) confirm an important depletion/sink of water column PAH in the photic zone, especially for low MW PAHs. Degradation processes in the water column may be responsible for this decoupling. Conversely, high MW PAHs dry deposition fluxes are similar to their settling fluxes.

Arsenic (As) reduction and translocation are key processes for As hyperaccumulation by the hyperaccumulator Pteris vittata L. Micro-X-ray adsorption spectroscopy of P. vittata’s rhizoid tissues revealed that As reduction mainly occurred in endodermis during translocation from epidermis to vascular bundle. Prior to reduction, arsenate (As (V)) translocation was an active process requiring energy and employing a phosphate (P) transporter. Use of a synchrotron X-ray microprobe showed that As (V) and P were cotransported and that this process could be enhanced by As (V) exposure or P deficiency but restrained by energy release inhibition caused by 2,4-dinitrophenol or sodium orthovanadate. In contrast, after As reduction, As(III) translocation differed from P translocation and was more efficient, appearing free from the apparent endodermal blockage. The results here revealed the role of the P transporter on As translocation as well as the key role of As reduction in As hyperaccumulation by P. vittata.