Stable C and N isotope abundances in water-extractable organic matter from air-dried soils as potential indices of microbially utilized organic matter

Stable carbon (C) and nitrogen (N) isotopes (13C and 15N) in water-extractable organic matter (WEOM) derived from air-dried soils may be applicable to elucidate the microbial decomposition of soil organic matter (SOM), which is crucial in terrestrial C cycles. A total of 40 soil samples were collected from a depth of 0–6 cm from a temperate broadleaved forest in Japan with vegetation succession from grassland approximately 150 years ago. Those soil samples were air-dried before the water extraction process and organic matter analysis. The C and N concentrations of WEOM were <3.6% of those of the bulk soil and were positively correlated with those of the bulk soil at a p-value of < 0.01. A positive correlation between the two fractions (i.e., WEOM and bulk soils) was also found for natural 13C and 15N abundances (δ13C and δ15N; p < 0.01). However, the C/N ratio of WEOM was slightly correlated with that of bulk soils, exhibiting a narrow range of values of ~10. Thus, those features of the WEOM were similar to the well-known features of microbial biomass. The δ13C and δ15N enrichments in WEOM relative to bulk soil, the difference in stable isotope abundances between bulk SOM and WEOM were negatively and positively correlated, respectively, with the concentrations of organo-mineral complexes and short-range order minerals (non-crystalline oxyhydroxides of aluminum and iron, allophane, imogolite, and allophane-like constituents), which play significant roles in SOM stabilization in soils. These relationships suggest that the stable isotopic enrichments in WEOM can be a good indicator of the microbial utilization of soil C and N under different substrate availabilities, which are crucial to SOM decomposition and decomposability substantially varying from local to global scales

Plastic-associated metal(loid)s in the urban river environments of Mongolia

The widespread distribution of plastic debris in riverine environment is one of the major concerns of environmental pollution because of its potential impact on the aquatic ecosystem. In this study, we investigated the accumulation of metal(loid)s on polystyrene foam (PSF) plastics collected from the floodplain of the Tuul River of Mongolia. The metal(loid)s sorbed on plastics were extracted from the collected PSF via sonication after peroxide oxidation. The size-dependent association of metal(loid)s with plastics indicates that PSFs act as vectors for pollutants in the urban river environment. The mean concentrations of metal(loid)s (i.e., B, Cr, Cu, Na, and Pb) indicate a higher accumulation of the metal(loid)s on meso-sized PSFs compared with macro- and micro-sized PSFs. In addition, the images from scanning electron microscopy (SEM) indicated not only the degraded surface of plastics showing fractures, holes, and pits but also the adhered mineral particles and microorganisms on the PSFs. The interaction of metal(loid)s with plastics was probably facilitated by the physical and chemical properties of altered surface of plastics through photodegradation, followed by an increase in surface area by size reduction and/or biofilm development in the aquatic environment. The enrichment ratio (ER) of metals on PSF samples suggested the continuous accumulation of heavy metals on plastics. Our results demonstrate that the widespread plastic debris could be a carrier of hazardous chemicals in the environment. Considering that the negative impacts of plastic debris on environmental health are major concerns to be addressed, the fate and behavior of the plastics especially their interaction with pollutants in aquatic environments should be further studied

Development of Field Estimation Technique and Improvement of Environmental Tritium Behavior Model

To estimate the environmental transfer of tritium into the atmosphere and to establish tritium analysis techniques, this study improves our previous compartment model and proposes new analytical technique based on the microwave heating method and a water-sample purification technique using ion resin. This article introduces a new conceptual approach for estimating environmental tritium behavior

Preliminary Investigation of Pretreatment Methods for Liquid Scintillation Measurements of Environmental Water Samples Using Ion Exchange Resins

This paper presents an evaluation of a rapid pretreatment method for tritium analysis, that uses ion exchange resins (the batch method). The standard water samples were prepared with river water collected in Okinawa, Japan. Powdex resin was used in this study, which is an ion exchange resins in the form of powder beads. First, 100 mL of the standard sample was stirred with the cation exchange (PCH) and anion exchange (PAO) resins, as well as with activated carbon. To determine the optimal stirring time, we tested stirring times of 5, 10, 20 and 30 min. Additionally, to determine a suitable amount of ion exchange resin for environmental water samples, variations in the amount of resin and activated carbon were tested. Under the conditions of Experiment-3 (0.3 g, 0.3 g and 0.6 g of PCH, PAO and activated carbon, respectively) and with a stirring time of 5 min, electrical conductivity values of less than 1 mSm^ were achieved. These results demonstrate the effectiveness of the removal of impurities in the sample water by ion exchange resins and confirm that such an effect can be achieved during a short period of time (i.e., in 5 min)

129I/127I ratios in Scottish coastal surface sea water: geographical and temporal responses to changing emissions

This work constitutes the first survey of I isotope ratios for Scottish sea water including the first data for the west of Scotland. These data are of importance because of the proximity to the world’s second largest emission source of 129I to the sea, the Sellafield nuclear reprocessing plant, because of the increasing importance of the sea to land transfer of 129I and also as input data for dose estimates based on this pathway of 129I. 129I/127I ratios in SW Scotland reached 3 × 10−6 in 2004. No strong variation of I isotope ratios was found from 2003 to 2005 in Scottish sea waters. Iodine isotope ratios increased by about a factor of 6 from 1992 to 2003 in NE Scotland, in agreement with the increase of liquid 129I emissions from Sellafield over that time period. It is demonstrated that 129I/127I ratios agree better than 129I concentrations for samples from similar locations taken in very close temporal proximity, indicating that this ratio is more appropriate to interpret than the radionuclide concentration

Development of Field Estimation Technique and Improvement of Environmental Tritium Behavior Model

To estimate the environmental transfer of tritium into the atmosphere and to establish tritium analysis techniques, this study improves our previous compartment model and proposes new analytical technique based on the microwave heating method and a water-sample purification technique using ion resin. This article introduces a new conceptual approach for estimating environmental tritium behavior

Preliminary Investigation of Pretreatment Methods for Liquid Scintillation Measurements of Environmental Water Samples Using Ion Exchange Resins

This paper presents an evaluation of a rapid pretreatment method for tritium analysis, that uses ion exchange resins (the batch method). The standard water samples were prepared with river water collected in Okinawa, Japan. Powdex resin was used in this study, which is an ion exchange resins in the form of powder beads. First, 100 mL of the standard sample was stirred with the cation exchange (PCH) and anion exchange (PAO) resins, as well as with activated carbon. To determine the optimal stirring time, we tested stirring times of 5, 10, 20 and 30 min. Additionally, to determine a suitable amount of ion exchange resin for environmental water samples, variations in the amount of resin and activated carbon were tested. Under the conditions of Experiment-3 (0.3 g, 0.3 g and 0.6 g of PCH, PAO and activated carbon, respectively) and with a stirring time of 5 min, electrical conductivity values of less than 1 mSm−1 were achieved. These results demonstrate the effectiveness of the removal of impurities in the sample water by ion exchange resins and confirm that such an effect can be achieved during a short period of time (i.e., in 5 min)