Effect of Si-rich substances on phosphorous adsorption by sandy soils

Environmental Science and Pollution Research - The poor adsorption capacity of sandy soils is one of the primary reasons of a high level of phosphorus (P) leaching. Silicon (Si)-rich soil...     

A spatial assessment of the forest carbon budget for Ukraine

Mitigation and Adaptation Strategies for Global Change - The spatial representation of forest cover and forest parameters is a prerequisite for undertaking a systems approach to the full and...     

Long-term changes of heavy metal and sulphur concentrations in ecosystems of the Taymyr Peninsula (Russian Federation) North of the Norilsk Industrial Complex

The Norilsk industrial ore smelting complex (Taymyr Peninsula, Russian Federation) has significantly impacted many components of local terrestrial and aquatic environments. Whether it has had a major impact on the wider Russian Arctic remains controversial as studies are scarce. From 1986 to 2004, data on heavy metal (Cu, Ni, Zn, Hg, Cd and Hg) concentrations in fish (burbot), moss, lichens, periphyton, hydric soils and snow in and around Norilsk and the most northern parts of the Taymyr Peninsula were analysed. Very high concentrations of Cu (203 μg L?1 ± 51 μg L?1) and Ni (113 μg L?1 ± 15 μg L?1) were found in the water of the Schuchya River close to Norilsk. Heavy metal concentrations in burbot liver were highest in Lake Pyasino near Norilsk compared to other study regions that were >100 km distant. From 1989-1996, Cu (121 μg L?1 ± 39 μg L?1 SD), Zn (150 μg L?1) ± 70 μg L?1) and Ni (149 μg L?1 ± 72 μg L?1) snow concentrations were greatest in Norilsk, but were low elsewhere. By 2004, these concentrations had dropped significantly, especially for Cu-74 μg L?1 (±18.7 μg L?1 SD), Zn-81.7 μg L?1 (± 31.3 μg L?1 SD) and Ni-80 μg L?1(±18.0 μg L?1 SD). Norilsk and its surroundings are subject to heavy pollution from the Norilsk metallurgical industry but these are absent from the greater Arctic region due to the prevailing winds and the Byrranga Mountains. Pollution abatement measures have been made so further investigations are necessary in order to assess their efficiency.     

Evaluation of 360 degree feedback ratings: relationships with each other and with performance and selection predictors

Feedback from 360 degree ratings based on competency principles and used for developmental purposes was investigated for interrelationships among the ratings and for its relationships with performance and selection data. Relationships among: (1) feedback ratings from supervisors, peers, and self; (2) feedback ratings and selection test data; and (3) feedback ratings and performance appraisals on about 2000 employees of a Midwestern insurance company were examined. The 360 ratings by peers and managers were related to performance appraisals. All significant correlations of manager and peer ratings with selection tests were positive, but significant correlations of 360 degree self‐ratings with selection tests were negative. Copyright © 2001 John Wiley & Sons, Ltd.     

Improved sample preparation and GC–MS analysis of priority organic pollutants

Mass spectrometry is a major tool for analysing organic pollutants. However, scientists often complain about laborious sample preparation. The development of new commercial high-resolution mass spectrometers gives a chance to improve simultaneously speed, reliability, and sensitivity of the analysis. Here, we used the time-of-flight high-resolution mass spectrometer Pegasus GC-HRT to identify and quantify 55 priority organic pollutants in water samples. This mass spectrometer has a high resolution of 50,000, a high mass accuracy of about 1 ppm and a very high acquisition rate of up to 200 full mass range spectra per second. 1 mL water samples were extracted with 1 mL dichloromethane. Results show that the sample preparation and analysis are achieved 30 times faster, requiring 1,000 times less water and 350 times less solvent than the classic 8270 method of the United States Environmental Protection Agency. The detection limit is 1 μg/L. The quantification limit is 10 μg/L. Our procedure, named accelerated water sample preparation, is simpler, faster, cheaper, safer and more reliable than 8270 Method.     

Solar energy harvesting in the epicuticle of the oriental hornet (Vespa orientalis)

The Oriental hornet worker correlates its digging activity with solar insolation. Solar radiation passes through the epicuticle, which exhibits a grating-like structure, and continues to pass through layers of the exo-endocuticle until it is absorbed by the pigment melanin in the brown-colored cuticle or xanthopterin in the yellow-colored cuticle. The correlation between digging activity and the ability of the cuticle to absorb part of the solar radiation implies that the Oriental hornet may harvest parts of the solar radiation. In this study, we explore this intriguing possibility by analyzing the biophysical properties of the cuticle. We use rigorous coupled wave analysis simulations to show that the cuticle surfaces are structured to reduced reflectance and act as diffraction gratings to trap light and increase the amount absorbed in the cuticle. A dye-sensitized solar cell (DSSC) was constructed in order to show the ability of xanthopterin to serve as a light-harvesting molecule.     

Rapid liquid–liquid extraction for the reliable GC/MS analysis of volatile priority pollutants

Mass spectrometry is a powerful tool for the analysis of organic pollutants in the environment. Nevertheless, sample preparation for GC/MS analysis is often criticized for being too laborious and requiring expensive equipment. Thus, purge-and-trap or headspace devices are the most popular nowadays to investigate volatile organic pollutants. At the same time, modern commercial high-resolution mass spectrometers allow for the significant simplification of the sample preparation procedures due to better acquisition rate, accurate mass measurements, and improved sensitivity. Here, we used a time-of-flight high-resolution mass spectrometer Pegasus GC-HRT (LECO, USA) to identify and quantify 47 volatile priority organic pollutants in water. The developed accelerated water sample preparation approach requires just 1 mL of water and 1 mL of dichloromethane. The detection limits of the analytes are about 1 μg L^?1, while the quantification limits are approximately 5 μg L^?1. These limits correspond to those required by Method 8260C of the United States Environmental Protection Agency. Here, we demonstrate that sample preparation for the reliable and sensitive GC/MS analysis of volatile organic priority pollutants may be achieved in 5 min in 5-mL vials in the field or just prior to GC/MS analysis in the laboratory without the use of any expensive equipment.