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From January to December 2010, surface snow samples were collected with monthly resolution at the Concordia station (75°06'S, 123°20'E), on the Antarctic plateau, and analysed for major and trace elements in both dissolved and particulate (i.e. insoluble particles, >0.45 μm) phase. Additional surface snow samples were collected with daily resolution, for the determination of sea-salt sodium and not-sea-salt calcium, in order to support the discussion on the seasonal variations of trace elements. Concentrations of alkaline and alkaline-earth elements were higher in winter (April-October) than in summer (November-March) by a factor of 1.2-3.3, in agreement with the higher concentration of sea-salt atmospheric particles reaching the Antarctic plateau during the winter. Similarly, trace elements were generally higher in winter by a factor of 1.2-1.5, whereas Al and Fe did not show any significant seasonal trend. Partitioning between dissolved and particulate phases did not change with the sampling period, but it depended only on the element: alkaline and alkaline-earth elements, as well as Co, Cu, Mn, Pb and Zn were for the most part (>80%) in the dissolved phase, whereas Al and Fe were mainly associated with the particulate phase (>80%) and Cd, Cr, V were nearly equally distributed between the phases. Finally, the estimated marine and crustal enrichment factors indicated that Cd, Cr, Cu, Pb and Zn have a dominant anthropogenic origin, with a possible contribution from the Concordia station activities.
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http://dx.doi.org/10.1016/j.chemosphere.2014.10.094 | DOI Listing |
Environ Pollut
September 2025
State Key Laboratory of Water Pollution Control and Green Resource Recycling, School of the Environment, Nanjing University, Nanjing 210023, Jiangsu, China. Electronic address:
o,p'-dichlorodiphenyltrichloroethane (2,4'-DDT) is a typical persistent organic pollutant (POP) characterized by environmental persistence and acute toxicity. Its pronounced hydrophobicity drives preferential adsorption onto suspended particulate matter (SPM) in aquatic systems. This study systematically investigated the photochemical transformation mechanism of 2,4'-DDT in the Pearl River SPM-water system.
View Article and Find Full Text PDFSci Total Environ
September 2025
Graduate School of Agriculture, Meijo University, 1-501 Shiogamaguchi, Nagoya 468-8502, Japan. Electronic address:
Halogenated polycyclic aromatic hydrocarbons (HPAHs) including chlorinated (ClPAHs) and brominated (BrPAHs) variants, are emerging contaminants that are considered the next-generation candidates of persistent organic pollutants. Since there was a significant gap exists in understanding of partitioning dynamics of HPAHs between the particulate phase (PP) and dissolved phase (DP) considering many congeners, this study analyzed 75 congeners of parent PAHs and HPAHs (p/HPAHs) in the samples collected from 27 sites from 20 water bodies in Sri Lanka. The results revealed that the mean of the total concentrations of PAHs, ClPAHs, and BrPAHs in the aqueous phase (PP + DP) were 55.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
Department of Chemistry & Chemical Biology, McMaster University, Hamilton, Ontario L8S 4M1, Canada.
Road dust, which consists of brake and tire wear, pavement particles, crustal material, semivolatile vehicle exhaust components, and natural organic matter, can contribute to both airborne particulate matter and urban runoff. To date, research has mainly focused on the health impact of road dust, but little work has been conducted to characterize its role as a reactive surface in the environment. Our group has previously shown that illuminated road dust is a source of singlet oxygen, an important environmental oxidant.
View Article and Find Full Text PDFBioresour Technol
September 2025
State Key Laboratory of Urban-rural Water Resource and Environment, School of Environment, Harbin Institute of Technology, No. 73, Huanghe Road, Nangang District, Harbin 150090, China. Electronic address:
The high-rate contact stabilization (HiCS) process enables energy-efficient carbon capture from wastewater, yet the interactions of contact phase parameters require clarification. This study systematically investigated the effects of contact time (Tc: 10 - 40 min) and dissolved oxygen concentration (DOc: below 0.2, 0.
View Article and Find Full Text PDFACS ES T Water
April 2025
Gerald May Department of Civil, Construction & Environmental Engineering, MSC01 1070, University of New Mexico, Albuquerque, New Mexico 87131, United States.
Understanding oxidized uranium [U(VI)] reactions with natural organic matter (NOM) is necessary to predict the solubility and mobility of U and NOM in waters from organically rich geologic uranium deposits influenced by natural and anthropogenic processes. Here, we investigated the changes in the chemical composition of NOM resulting from its reaction with U(VI) under acidic and neutral pH under controlled laboratory conditions. We employed a multianalytical approach, including X-ray photoelectron spectroscopy (XPS), Fourier transform ion cyclotron resonance-mass spectrometry (FTICR-MS), transmission electron microscopy (TEM), and X-ray absorption spectroscopy (XAS).
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