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Acid deposition is widespread in Japan, but acidification of stream water is rare in forest ecosystems. Bedrock‐derived cations, including those released into the soil by weathering of bedrock minerals, generally act to neutralize acid deposition and flow out into streams. Volcanic ash, which is widespread in Japan, may also release cations and neutralize acids, but the contribution of volcanic‐ash‐derived cations is currently poorly explored. To assess the importance of volcanic ash as a source of base cations, we examined strontium in two catchments underlain by chert bedrock at Mount Amamaki, Japan. Additionally, we obtained comparative data from two sandstone‐bedrock catchments in the same area. We measured 87Sr/86Sr ratios in samples of stream water, bulk precipitation, riverbed rock, and soil from the catchments. We used the 87Sr/86Sr data to analyze the relative contributions of atmospheric deposition, bedrock, and volcanic ash in soil as sources of Sr in the stream waters. We estimated volcanic ash in soil to contribute between 46% and 78% of stream‐water Sr for one chert‐bedrock catchment, and between 0% and 52% for the other. We conclude that volcanic ash in soil is an important source of Sr in stream water. Thus, volcanic ash can act as a source of base cations and hence contribute to the acid‐neutralizing capacity of soil in forest ecosystems in Japan. [ABSTRACT FROM AUTHOR]

Collection and cooking of wild vegetables have provided seasonal enjoyments for Japanese local people as provisioning and cultural ecosystem services. However, the Fukushima Daiichi Nuclear Power Plant accident in March 2011 caused extensive radiocesium contamination of wild vegetables. Restrictions on commercial shipments of wild vegetables have been in place for the last 10 years. Some species, including buds of Aralia elata, are currently showing radiocesium concentrations both above and below the Japanese reference level for food (100 Bq/kg), implying that there are factors decreasing and increasing the 137Cs concentration. Here, we evaluated easy-to-measure environmental variables (dose rate at the soil surface, organic soil layer thickness, slope steepness, and presence/absence of decontamination practices) and the 137Cs concentrations of 40 A. elata buds at 38 locations in Fukushima Prefecture to provide helpful information on avoiding collecting highly contaminated buds. The 137Cs concentrations in A. elata buds ranged from 1 to 6,280 Bq/kg fresh weight and increased significantly with increases in the dose rate at the soil surface (0.10–6.50 μSv/h). Meanwhile, the 137Cs concentration in A. elata buds were not reduced by decontamination practices. These findings suggest that measuring the latest dose rate at the soil surface at the base of A. elata plants is a helpful way to avoid collecting buds with higher 137Cs concentrations and aid in the management of species in polluted regions. [ABSTRACT FROM AUTHOR]

A two‐stage sampler was designed to investigate the vertical distribution of heavy metals and trace elements that contaminate forest soils through atmospheric deposition. The hand‐corer consisted of two L‐shaped aluminum angles that were driven separately into the soil to reduce friction between the corer wall and the soil. This allowed for soil cores to be collected with less compression than with traditional corers. The corer is easily made, inexpensive, lightweight, and easy to carry. The degree of compression of soil cores collected at a depth of 20 cm from various montane forests in Japan was usually less than 10% (collected core length >18 cm); although, more compression occurred in soil with a higher air content. The degree of compression of soil cores collected from urban forests was lower than that in montane forests. When the two‐stage sampler was compared with a tube‐type sampler in a Japanese cedar (Cryptomeria japonica) forest, the compression degree of a soil core collected with the two‐stage sampler was a quarter that of the tube‐type sampler. The collection of less‐compressed soil cores will allow for reconstruction of a more accurate linear depth distribution of contaminants. To demonstrate this, we investigated the vertical distribution of Pb, Sb, and radioactive 137Cs in soil cores collected from conifer plantations on Mount Tsukuba, Japan, in April 2011. The migration centers of anthropogenic Pb, Sb, and 137Cs were positioned at 7.9, 7.5, and 3.3 cm from the ground surface, respectively. These distances probably reflect differences in the history of atmospheric pollution. [ABSTRACT FROM AUTHOR]

The aggregated transfer factor (Tag) is commonly used to represent the actual transfer of radiocesium from soil to wild edible plants, but the values have shown substantial variation since the Fukushima nuclear accident. To elucidate the factors causing this variation, we investigated the effects of spatial scale and vertical 137Cs distribution in the soil on the variation of Tag-137Cs values for one of the most severely contaminated wild edible plants, Eleutherococcus sciadophylloides Franch. et Sav. (Koshiabura). The variation in Tag-137Cs values was not reduced by direct measurement of 137Cs deposition in soil samples from the Koshiabura habitat, as a substitute for using spatially averaged airborne survey data at the administrative district scale. The 137Cs activity concentration in Koshiabura buds showed a significant positive correlation with the 137Cs inventories only in the organic horizon of soil from the Koshiabura habitat. The ratio of 137Cs inventories in the organic horizon to the total 137Cs deposition in soil exhibited substantial variation, especially in broad-leaved deciduous forests that Koshiabura primarily inhabits. This variation may be the cause of the wide range of Tag-137Cs values observed in Koshiabura buds when calculated from the total 137Cs deposition in soil. [ABSTRACT FROM AUTHOR]

A heterogeneous chiral imidazolodinone catalyst was synthesized by immobilization on a sulfated chitin through non‐covalent ionic interactions. The chitin‐based organocatalyst promoted the asymmetric Diels‐Alder reaction with high enantioselectivity under heterogeneous conditions and was successfully reused multiple times without apparent loss of catalytic activity and enantioselectivity. [ABSTRACT FROM AUTHOR]

Heterogeneous multiple‐catalyst assemblies were developed in which the flavinium cation and Na or Li cations were easily immobilized on a chitin‐derived anionic polymeric scaffold through noncovalent ionic interactions. The supramolecular flavinium catalysts were successfully employed in the environmentally friendly heterogeneous Baeyer–Villiger oxidation and sulfoxidation by H2O2. Owing to the cooperative catalytic effect of flavinium, alkali metal, and sulfated chitin, the supramolecular flavinium assembly showed higher catalytic activity for the Baeyer–Villiger oxidation of cyclic ketones than the corresponding homogeneous flavinium catalyst. Because the ionic assembly was stable under the reaction conditions, the catalyst could be readily recovered by simple filtration and reused. [ABSTRACT FROM AUTHOR]