Activity concentrations of 137Cs were detected in more than 400 outer spruce bark samples collected at sites variably affected by Chernobyl fallout across the Czech Republic in 1995 and 2010. The temporal changes in the 137Cs activities were found. The mean effective half-life (TEF) for 137Cs in spruce bark was 9.6 years, and the mean environmental half-life (TE) was 14 years. The effective half-lives were significantly higher in areas with higher long-term annual precipitation sums. Coefficient a in linear regression y = ax + b of half-lives on precipitation sums was 0.015 y mm−1 for TEF and 0.036 y mm−1 for TE. The aggregated transfer factor of 137Cs from soil to bark was determined and the pre-Chernobyl bark contamination related to year 2010 was estimated.

With the aim of investigating the effects of carbonaceous sorbent amendment on plant health and end point contaminant bioavailability, plant experiments were set up to grow maize (Zea mays) in soil contaminated with polycyclic aromatic hydrocarbons (PAHs) and metals. Maize and pine derived biochars, as well as a commercial grade activated carbon, were used as amendments. Plant growth characteristics, such as chlorophyll content and shoot to root biomass, improved with sorbent amendment to varying extents and contaminant uptake to shoots was consistently reduced in amended soils. By further defining the conditions in which sorbent amended soils successfully reduce contaminant bioavailability and improve plant growth, this work will inform field scale remediation efforts.

Concentration and enantiomeric fractions (EFs) of chiral chlorinated pesticides (α-hexachlorocyclohexane (α-HCH), trans-, cis- and oxychlordane) were determined in Arctic zooplankton, mainly Calanus spp. collected in the period 2007–11 from Svalbard fjords and open pack-ice. The temporal and spatial enantiomer distribution varied considerably for all species and chiral pesticides investigated. An overall enantiomeric excess of (+)-oxychlordane (EF 0.53–0.86) were observed. Cis-chlordane was close to racemic (EF 0.46–0.55), while EF for trans-chlordane varied between 0.29 and 0.55, and between 0.38 and 0.59 for α-HCH. The biodegradation potential for trans-chlordane was higher compared to cis-chlordane. The comprehensive statistical evaluation of the data set revealed that the EF distribution of α-HCH was affected by ice cover to a higher extent compared to cis-chlordane. Potential impact from benthic processes on EFs in zooplankton is an interesting feature and should be further investigated. Enantiomeric selective analyses may be a suitable tool for investigations of climate change related influences on Arctic ecosystems.

Uptake and elimination kinetics of metals in soil invertebrates are a function of both soil and organism properties. This study critically reviewed metal toxicokinetics in soil invertebrates and its potential use for assessing bioavailability. Uptake and elimination rate constants of different metals are summarized. Invertebrates have different strategies for essential and non-essential metals. As a consequence, different types of models must be applied to describe metal uptake and elimination kinetics. We discuss model parameters for each metal separately and show how they are influenced by exposure concentrations and by physiological properties of the organisms. Soil pH, cation exchange capacity, clay and organic matter content significantly affect uptake rates of non-essential metals in soil invertebrates. For essential metals, kinetics is hardly influenced by soil properties, but rather prone to physiological regulation mechanisms of the organisms. Our analysis illustrates that toxicokinetics can be a valuable measurement to assess bioavailability of soil-bound metals.

This review provides a summary of studies analysing metal concentrations in soils and soil solution at European roadsides. The data collected during 27 studies covering a total of 64 sites across a number of European countries were summarised. Highest median values of Cr, Cu, Ni, Pb, and Zn were determined in the top soil layer at the first 5 m beside the road. Generally, the influence of traffic on soil contamination decreased with increasing soil depth and distance to the road. The concentration patterns of metals in soil solution were independent from concentrations in the soil matrix. At 10-m distance, elevated soil metal concentrations, low pH, and low percolation rates led to high solute concentrations. Directly beside the road, high percolation rates lead to high annual loadings although solute concentrations are comparatively low. These loadings might be problematic, especially in regions with acidic sandy soils and a high groundwater table.

Concentrations of NO2 and O3 were measured inside and outside a dense broad-leaved forest canopy adjacent to a busy traffic route in the City of Gothenburg, Sweden, with duplicate passive diffusion samplers during six one-week periods starting well before leaf senescence and ending when leaves were largely senescent. Concentrations of NO2 were lower inside the forest canopy during all periods (representing a significant effect, p = 0.016), on average by 7% or 2.7 μg m−3. O3 showed a more variable response with an average non-significant effect of 2% lower in the forest stand. There was no systematic trend of the difference in concentrations inside and outside the forest stand of the pollutants with the progression of autumn leaf senescence. Our study indicates that the effect of urban vegetation on air pollution concentrations is small, although it seems to exist for NO2 in a traffic polluted environment.

Understanding temporal and spatial variation in soil chemicals is critical in exposure assessments. We measured eight metals in subsamples, duplicates (∼0.3 m), and repeat soil samples taken 1–6 years after initial sampling (∼5 m). We estimated variance components (VCs) of metal concentrations using nested analyses accounting for sampling area, land use and soil type, and calculated coefficients of variation (CVs) for repeat sample pairs. Total variance for all metals was similar, but VCs were proportioned differently by metal and sample type. Spatial variation explained the majority of variance in duplicate samples. CVs of metal concentrations were not significantly different over the long time interval, but repeat samples had larger VCs for unexplained error. Sampling area and land use were important for Ba and Mn, and Pb and Hg, respectively. Results suggest metals are stable over long times and suitable for exposure assessments, but that individual metal behavior should be considered.

Surface carbon dioxide concentrations were measured using a non-dispersive infrared carbon dioxide sensor at Lampang Rajabhat University from April to May 2013 and at the University of the Philippines-Diliman campus starting September 2013. Factors influencing the variations in these measurements were determined using multiple linear regression and a Lagrangian transport model. Air temperature and sea level pressure were the dominant meteorological factors that affect the CO2 variations. However, these factors are not enough. Surface CO2 flux and transboundary transport needs to be considered as well.