Aminocyclopyrachlor is a pyrimidine carboxylic acid herbicide used to control broadleaf weeds and brush. Amending soil with activated charcoal is recommended to prevent off-site transport of aminocyclopyrachlor and non-target plant damage. We used the batch-equilibrium method to determine the concentration of aminocyclopyrachlor in a pseudo-steady state with biochar, soil, and biochar-soil systems (<10% biochar by weight). We observed that aminocyclopyrachlor is mobile in soils. Soil incorporation of activated charcoal removed nearly all of the aqueous aminocyclopyrachlor thereby limiting its bioavailability to non-target flora. On the other hand, biochars were less effective than activated charcoal. Biochar produced from olive mill waste feedstock was the most effective biochar that we assessed for reducing the aqueous herbicide concentration. Although these biochars reduced the aminocyclopyrachlor concentration, they would not be practical remediation media due to the extraordinarily high application rates required to reduce the concentration by 50% (2.13 × 105 kg ha−1–7.27 × 105 kg ha−1).

Silver fir is one of the most productive and ecologically valuable native European tree species, however, it has been experiencing decline which has periodically occurred over its natural range. This paper aims to investigate the recent climate–growth relationships of silver fir (Abies alba Mill.) and its temporal change along the course of its life. Long-term tree-ring databases, as well as records on climate, atmospheric SO2, NO3 and acid concentrations from four different regions in the Western Carpathians were used. The results provide clear evidence of significant increase of silver fir's radial increment over the entire Western Carpathian area since 1970–1980. The results indicated that the most probable factors behind the rapid recovery of tree radial increment were reductions in emissions of NO3 and SO2, alongside a significant increase in mean June, July and April temperatures.

In order to characterize polybrominated diphenyl ethers (PBDEs), and hydroxylated and methoxylated PBDEs (OH-PBDEs and MeO-PBDEs) in the soil–plant system, soil and plant samples were collected from an e-waste recycling area in China. Forty one PBDEs, twelve OH-PBDEs and MeO-PBDEs were detected in the soil and plant samples. Concentrations of PBDEs in roots were significantly correlated to their concentrations in the soils, but the percentages of lower brominated congeners in the plants were higher than those in the soils. Significant positive linear relationships exist between concentrations of ∑OH-PBDEs and ∑MeO-PBDEs with higher levels of ∑MeO-PBDEs than those of ∑OH-PBDEs in the soils, plant roots and leaves. A majority of the OH-/MeO-PBDEs had the hydroxyl or methoxy group at the ortho-positions to the biphenyl bond for most of the plant species. However the occurrence of meta- and para- substituted OH-/MeO-PBDEs in soils and plants were also confirmed.

Serum and urine samples from 120 children aged 5–13 years from Dae-gu, Korea, were analyzed for 16 perfluorinated compounds (PFCs). The total PFC concentrations in the serum were 4.26–29.70 ng/mL, and perfluorohexanesulfonate (PFHxS), perfluorooctanoic acid (PFOA), perfluorooctanesulfonate (PFOS, which was dominant overall, at 6.58 ng/mL), and perfluoroundecanoic acid (PFUndA) were detected in all serum samples. The total PFC concentrations in the urine ranged from below the detection limit to 14.9 ng/mL, and perfluoropentanoic acid (PFPeA) was predominant. The PFOS (p < 0.005) concentration was higher in the serum of children than that of Korean adults aged 20–29. Some of the PFC concentrations in the serum correlated negatively with body mass index and tended to increase with the duration of breastfeeding. However, there were no gender-specific differences in the PFC concentrations and no correlations between PFC concentrations in serum and urine.

Rainfall-triggered runoff is a major driver of pesticide input in streams. Only few studies have examined the suitability of passive sampling to quantify such episodic exposures. In this study, we used Empore™ styrene-divinylbenzene reverse phase sulfonated disks (SDB disks) and event-driven water samples (EDS) to assess exposure to 15 fungicides and 4 insecticides in 17 streams in a German vineyard area during 4 rainfall events. We also conducted a microcosm experiment to determine the SDB-disk sampling rates and provide a free-software solution to derive sampling rates under time-variable exposure. Sampling rates ranged from 0.26 to 0.77 L d−1 and time-weighted average (TWA) concentrations from 0.05 to 2.11 μg/L. The 2 sampling systems were in good agreement and EDS exceeded TWA concentrations on average by a factor of 3. Our study demonstrates that passive sampling is suitable to quantify episodic exposures from polar organic pesticides.

The potential benefit of urban vegetation in reducing heat related mortality in the city of Melbourne, Australia is investigated using a two-scale modelling approach. A meso-scale urban climate model was used to quantify the effects of ten urban vegetation schemes on the current climate in 2009 and future climates in 2030 and 2050. The indoor thermal performance of five residential buildings was then simulated using a building simulation tool with the local meso-climates associated with various urban vegetation schemes. Simulation results suggest that average seasonal summer temperatures can be reduced in the range of around 0.5 and 2 °C if the city were replaced by vegetated suburbs and parklands, respectively. With the limited buildings and local meso-climates investigated in this study, around 5–28% and 37–99% reduction in heat related mortality rate have been estimated by doubling the city's vegetation coverage and transforming the city into parklands respectively.

To determine the effects of ozone (O3) on the canopy carbon budget, we investigated photosynthesis and respiration of leaves of Siebold's beech saplings under free air O3 exposure (60 nmol mol−1, during daytime) in relation to the within-canopy light gradient; we then calculated the canopy-level photosynthetic carbon gain (PCG) and respiratory carbon loss (RCL) using a canopy photosynthesis model. Susceptibilities of photosynthesis and respiration to O3 were greater in leaves of upper canopy than in the lower canopy. The canopy net carbon gain (NCG) was reduced by O3 by 12.4% during one growing season. The increased RCL was the main factor for the O3-induced reduction in NCG in late summer, while contributions of the reduced PCG and the increased RCL to the NCG were almost the same in autumn. These results indicate contributions of changes in PCG and RCL under O3 to NCG were different between seasons.

Hydroxylated (OH-) and methoxylated (MeO-) polybrominated diphenyl ethers (PBDEs) have caused much concern because of their potential toxicity and worldwide distribution. These compounds are recently suggested to originate from the natural process in the ocean. However, their source remains highly controversial. In this study, we analyzed the contents of nine MeO-BDEs, ten OH-BDEs, and phytoplankton biomarkers (PBs) in two sediment cores collected from the East China Sea (ECS). The detection of 6-MeO-BDE-47, 2′-MeO-BDE-68, and 6-OH-BDE-47 have been reported since the 1920s, prior to the production of PBDEs. Significant relations were found between MeO/OH-BDEs and indicators of marine organic matters. The similar down-core variations and significant correlations between MeO/OH-BDEs and PBs suggest the possibility that phytoplankton produced these natural compounds. Laboratory incubation further demonstrates that phytoplankton can produce MeO-BDEs. Comparisons between the content ratios of 6-MeO-BDE-47/2′-MeO-BDE-68 and brassicasterol/dinosterol indicate that the signature of MeO-BDEs is controlled by the phytoplankton community structure.

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.