1. |
- Rämö, Robert, et al.
(författare)
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Sediment Remediation Using Activated Carbon: Effects of Sorbent Particle Size and Resuspension on Sequestration of Metals and Organic Contaminants.
- 2022
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Ingår i: Environmental toxicology and chemistry. - : Wiley. - 1552-8618 .- 0730-7268. ; 41:4, s. 1096-1110
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Tidskriftsartikel (refereegranskat)abstract
- Thin-layer capping using activated carbon (AC) has been described as a cost-effective in situ sediment remediation method for organic contaminants. In this study, we compare the capping efficiency of powdered AC (PAC) against granular AC (GAC) using contaminated sediment from Oskarshamn harbor, Sweden. The effects of resuspension on contaminant retention and cap integrity were also studied. Intact sediment cores were collected from the outer harbor and brought to the laboratory. Three thin-layer caps, consisting of PAC or GAC mixed with clay, or clay only, were added to the sediment surface. Resuspension was created using a motor-driven paddle to simulate propeller wash from ship traffic. Passive samplers were placed in the sediment and in the water column to measure the sediment-to-water release of PAHs, PCBs, and metals. Our results show that a thin-layer cap with PAC reduced sediment-to-water fluxes of PCBs by 57 % under static conditions and 91 % under resuspension. Thin-layer capping with GAC was less effective than PAC, but reduced fluxes of high-molecular weight PAHs. Thin-layer capping with AC was less effective in retaining metals, except for Cd, which release was significantly reduced by PAC. Resuspension generally decreased water concentrations of dissolved cationic metals, perhaps due to sorption to suspended sediment particles. Sediment resuspension in treatments without capping increased fluxes of PCBs with log Kow > 7 and PAHs with log Kow 5 6, but resuspension reduced PCB and PAH fluxes through the PAC thin-layer cap. Overall, PAC performed better than GAC, but adverse effects on the benthic community and transport of PAC to non-target areas are drawbacks that favor the use of GAC. This article is protected by copyright. All rights reserved.© 2022 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
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2. |
- Arellano, Santiago, 1981
(författare)
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Studies of Volcanic Plumes with Remote Spectroscopic Sensing Techniques -DOAS and FTIR measurements on volcanoes of the Network for Observation of Volcanic and Atmospheric Change-
- 2014
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Volcanism is a rich geodynamical process, closely linked to the origin and ongoing evolution of the lithosphere, atmosphere, hydrosphere and biosphere. Humans have benefited from the resources provided by volcanoes but also been threatened by the dangers of volcanic eruptions, which accurate prediction remains elusive. This is partly due to the inherent complexity of volcanic systems and partly because of the difficulty of conducting key observations to characterize them. In particular, since the segregation and escape of magmatic volatiles are essential mechanisms behind volcanic eruptions, monitoring the intensity and composition of the resulting emissions in the atmosphere is essential to characterize the state of volcanic activity; however, their direct measurement is not always feasible.Remote spectroscopic sensing, whereby gas species can be quantified by their spectral signatures in electromagnetic radiation gathered at a prudent distance from the plume, offers the possibility to conduct reliable and sustainable monitoring of volcanic emissions. To expand the remote sensing capabilities of volcanological observatories the Network for Observation of Volcanic and Atmospheric Change (NOVAC) was established in 2005. The central theme of this thesis is the acquisition, analysis and interpretation of measurements of volcanic gas emissions on volcanoes of NOVAC. Measurements of the mass flow rate of SO2 and the molar ratios of SO2 against BrO and HCl were obtained by scanning-Differential Optical Absorption Spectroscopy (DOAS) of scattered solar ultraviolet radiation and by Fourier-Transform Spectroscopy (FTIR) of direct solar infrared radiation. The uncertainty of the measurements is characterized and methods for combining observations from different sensors implemented. Statistical and physical models of degassing are proposed for selected volcanoes of the network. The resulting time-series of emission on 16 volcanoes is one of the more detailed compilations of volcanic degassing in the last decade, particularly from passive emissions which are difficult to detect from satellite platforms. This work aims at advancing our knowledge of volcanic eruptions for a better mitigation of their risks.
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3. |
- Baresel, Christian, et al.
(författare)
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Uncertainty-Accounting Environmental Policy and Management of Water Systems
- 2007
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Ingår i: Environmental Science & Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 41:10, s. 3653–3659-
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Tidskriftsartikel (refereegranskat)abstract
- Environmental policies for water quality and ecosystemmanagement do not commonly require explicit stochasticaccounts of uncertainty and risk associated with thequantification and prediction of waterborne pollutant loadsand abatement effects. In this study, we formulate andinvestigate a possible environmental policy that does requirean explicit stochastic uncertainty account. We compareboth the environmental and economic resource allocationperformance of such an uncertainty-accounting environmentalpolicy with that of deterministic, risk-prone and riskaverseenvironmental policies under a range of differenthypothetical, yet still possible, scenarios. The comparisonindicates that a stochastic uncertainty-accountingpolicy may perform better than deterministic policies overa range of different scenarios. Even in the absence ofreliable site-specific data, reported literature values appearto be useful for such a stochastic account of uncertainty.
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4. |
- Drake, Henrik, et al.
(författare)
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Extreme fractionation and micro-scale variation of sulphur isotopes during bacterial sulphate reduction in deep groundwater systems
- 2015
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Ingår i: Geochimica Et Cosmochimica Acta. - : Elsevier BV. - 0016-7037 .- 1872-9533. ; 161, s. 1-18
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Tidskriftsartikel (refereegranskat)abstract
- This study conducted at the Aspo Hard Rock Laboratory, SE Sweden, determines the extent and mechanisms of sulphur-isotope fractionation in permanently reducing groundwater in fractured crystalline rock. Two boreholes > 400 m below the ground surface were investigated. In the 17-year-old boreholes, the Al instrumentation pipes had corroded locally (i.e., Al[oxy] hydroxides had formed) and minerals (i.e., pyrite, iron monosulphide, and calcite) had precipitated on various parts on the equipment. By chemically and isotopically comparing the precipitates on the withdrawn instrumentation and the borehole waters, we gained new insight into the dynamics of sulphate reduction, sulphide precipitation, and sulphur-isotope fractionation in deep-seated crystalline-rock settings. An astonishing feature of the pyrite is its huge variability in delta S-34, which can exceed 100 parts per thousand in total (i.e., -47.2 to +53.3 parts per thousand) and 60 parts per thousand over 50 mu m of growth in a single crystal. The values at the low end of the range are up to 71 parts per thousand lower than measured in the dissolved sulphate in the water (20-30 parts per thousand), which is larger than the maximum difference reported between sulphate and sulphide in pure-culture experiments (66 parts per thousand) but within the range reported from natural sedimentary settings. Although single-step reduction seems likely, further studies are needed to rule out the effects of possible S disproportionation. The values at the high end of the range (i.e., high delta S-34(py)) are much higher than could be produced from the measured sulphate under any biogeochemical conditions. This strongly suggests the development of closed-system conditions near the growing pyrite, i.e., the rate of sulphate reduction exceeds the rate of sulphate diffusion in the local fluid near the pyrite, causing the local aqueous phase (and thus the forming pyrite) to become successively enriched in heavy S (S-34). Consequently, the delta S-34 values of the forming pyrite become exceptionally high and strongly decoupled from the delta S-34 values of the sulphate in the bulk fluid. The Al-(oxy) hydroxide and calcite precipitates are explained by a combination of deposit and galvanic corrosion initiated by Al corrosion by H2S produced by sulphate-reducing microorganisms. (C) 2015 Elsevier Ltd. All rights reserved.
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5. |
- Eveborn, David, 1978-, et al.
(författare)
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Phosphorus in soil treatment systems : accumulation and mobility
- 2014
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Ingår i: Water Research. - : Elsevier. - 0043-1354 .- 1879-2448. ; 64, s. 42-52
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Tidskriftsartikel (refereegranskat)abstract
- In several western countries, septic tanks with subsequent soil treatment systems (STS) are a common treatment technique for domestic wastewater in rural areas. However the suitability of STS (especially relatively close to surface waters) can be questioned since the discharge of phosphorus (P) from such effluents is not well known. In this study, six STS in Sweden (11 to 28 years old) were investigated by means of batch and column experiments on samples taken from the unsaturated subsoil beneath the distribution pipes. At all sites the wastewater had clearly influenced the soil. This was observed through decreased pH, increased amounts of oxalate extractable metals and altered P sorption properties. The amount of accumulated P in the STS (defined as the amount of total P in the STS samples minus the amount of total P in unused soil samples) were found to be between 0.32 and 0.87 kg m-3, which in most cases was just a small fraction of the estimated P load (< 30%). Column studies revealed that remarkably high P concentrations (up to 6 mg L-1) were leached from the material when deionized water was applied. However, the response to deionized water varied between the sites. The affinity for P in the soils was well correlated to the amount of oxalate-extractable aluminium (as evidenced by a strong relationship between oxalate-extractable Al and oxalate-extractable P) and generally soils with high content of oxalate extractable Al was also less vulnerable to P leakage.
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6. |
- Ghosh, Devanita
(författare)
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Distribution and Biogeochemical Cycling of Arsenic In Grey and Brown Sand Aquifers in the Bengal Delta Plains (India)
- 2016
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- An elevated level of Arsenic (As) in aquifers from India and Bangladesh affecting the human health has been widely reported since the late 1980s. The thesis aim is to investigate the present status of As contamination and biogeochemical cycling with direct role of diverse indigenous bacterial communities in As cycling in the Bengal Delta Plain (BDP) aquifers in Nadia district, West Bengal (India). The As(III) oxidizing bacterial communities were predominant in grey sand aquifers (GSA), but were characteristically absent in brown sand aquifers (BSA). Rainwater recharge containing inorganic and organic dissolved compounds played an important role in shaping the different groups of bacterial phenotypes. It included thearsenite-oxidizing bacteria as revealed by the aioA and 16S rRNA phylogeny. These bacterial communities in BDP groundwater were assumed to utilize the dissolved and sedimentary organic carbon (DOC and SOC) as the primary carbon source for respiration, and remobilization/immobilization of As involving reductive dissolution of iron oxyhydroxides. Hence, sediment and groundwater of these aquifer waters were characterized for their different inorganic constituents (metals) and organic compound classes. There were notable differences between the groundwater DOC and SOC pools. The only similarity between these carbon pools is presence of petroleum-derived hydrocarbons. The SOC in BSA has good correlation with the clay and silt-rich fraction. Notably, As formed complexes with iron, but not manganese. Biomarker characterization in sediments showed presence of terrigenous inputs along with petroleum-derived hydrocarbons. However, these hydrocarbons were absent in BSA sediments, and so were the arsenite oxidizing bacterial communities. Although DOC in groundwater plays an important role in sustaining the microorganisms, the contrasting character of SOC in BSA and GSA strongly influence the shaping of microbial community structure and biogeochemical cycling of As. This particularly affects the natural ‘safe’ drinking water capacity. Overall, the study gives a new directionfor long-term research on As biogeochemical cycling in the contaminated BDP aquifers.
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7. |
- Routh, Joyanto, 1968-, et al.
(författare)
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Trace-element geochemistry of Onion Creek near Van Stone lead-zinc mine (Washington, USA) — Chemical analysis and geochemical modeling
- 1996
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Ingår i: Chemical Geology. - : Elsevier. - 0009-2541 .- 1872-6836. ; 133:1, s. 211-224
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Tidskriftsartikel (refereegranskat)abstract
- Van Stone lead-zinc mine in Washington is a possible contamination source of Columbia River water. Breaching of an old tailings pond, seepage of contaminated water, and surficial transport of mine tailings have increased trace-element (TE) concentrations in the Onion Creek water and sediments. Chemical analyses of water and sediment samples indicate high TE levels near the breached tailings pond. TE contamination indices for sediments indicate high values of Pb, Zn, and other TE’s which decrease downstream. High Kd values (> 104) for several TE’s (e.g., Al, Cd, Fe, Mn, Pb, V, and Zn) suggest their enrichment in the solid phase. TE concentrations in Onion Creek water and sediment sharply attenuate downstream due to: (1) enhanced carbonate dissolution, thereby increasing pH and immobilizing TE’s; (2) sorption to oxides; and (3) change in lithology from carbonate to granite. Speciation model MINTEQA2 was used to study the effect on TE dispersion due to dissolution-precipitation reactions and adsorption to ferrihydrite. In addition to the field and chemical data, the model also supports the hypothesis that Onion Creek sediments are the major sink for TE’s at VSM. Model runs indicate precipitation of Al, Ba, Ca, Fe, Mg, and Mn minerals from oversaturation, whereas TE’s with low concentrations (Cr, Cu, Ni, Se) or geochemically more mobile (As, Mo, Sb) remain dissolved in water. Near the tailings ponds, high pH and abundance of sorption sites in sediments contribute to the complete adsorption of Pb and Zn species. Because ambient conditions result in the sorption of most Pb and Zn ions, Onion Creek water quality meets EPA regulatory standards. These species will persist in Onion Creek sediments as sorbed or insoluble complexes, and without drastic pH changes (< 4.0) they will remain immobilized. However, continued TE enrichment in sediments will prove hazardous to filter feeding and aquatic organisms.
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8. |
- Jiang, Tao, et al.
(författare)
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Influence of dissolved organic matter (DOM) characteristics on dissolved mercury (Hg) species composition in sediment porewater of lakes from southwest China
- 2018
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Ingår i: Water Research. - : Elsevier. - 0043-1354 .- 1879-2448. ; 146, s. 146-158
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Tidskriftsartikel (refereegranskat)abstract
- The origin and composition of dissolved organic matter (DOM) in porewater of lake sediments is intricate and decisive for fate of pollutants including mercury (Hg). While there are many reports on the relationship between dissolved organic carbon concentration (DOC) and mercury (Hg) concentrations in aquatic systems, there are few in which DOM compositional properties, that may better explain the fate of Hg, have been the focus. In this study, porewaters from sediments of three lakes, Caihai Lake (CH), Hongfeng Lake (HF) and Wujiangdu Lake (WJD), all located in southwest China, were selected to test the hypothesis that DOM optical properties control the fate of Hg in aquatic ecosystems. Porewater DOM was extracted and characterized by UV-Vis absorption and fluorescence spectroscopy. A two end-member (autochthonous and allochthonous DOM) mixing model was used to unveil the origin of DOM in porewaters of the three lakes. Our results show a higher input of terrestrial DOM in the pristine lake CH, as compared to lakes HF and WJD lakes, which were both influenced by urban environments and enriched in autochthonous DOM. While the relationships between the concentrations of DOC and the different chemical forms of Hg forms were quite inconsistent, we found important links between specific DOM components and the fate of Hg in the three lakes. In particular, our results suggest that allochthonous, terrestrial DOM inhibits Hg(II) availability for Hg methylating micro-organisms. In contrast, autochthonous DOM seems to have been stimulated MeHg formation, likely by enhancing the activity of microbial communities. Indeed, DOM biodegradation experiments revealed that differences in the microbial activity could explain the variation in the concentration of MeHg. While relationships between concentrations of DOC and Hg vary among different sites and provide little information about Hg cycling, we conclude that the transport and transformation of Hg (e.g. the methylation process) are more strongly linked to DOM chemical composition and reactivity.
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9. |
- Fornieles-Callejon, J., et al.
(författare)
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Extremely low frequency band station for natural electromagnetic noise measurement
- 2015
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Ingår i: Radio Science. - 0048-6604 .- 1944-799X. ; 50:3, s. 191-201
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Tidskriftsartikel (refereegranskat)abstract
- A new permanent ELF measurement station has been deployed in Sierra Nevada, Spain. It is composed of two magnetometers, oriented NS and EW, respectively. At 10 Hz, their sensitivity is 19 V/pT and the signal-to-noise ratio (SNR) is 28 dB for a time-varying signal of 1 pT, the expected field amplitude in Sierra Nevada. The station operates for frequencies below 24 Hz. The magnetometers, together with their corresponding electronics, have been specifically designed to achieve such an SNR for small signals. They are based on high-resolution search coils with ferromagnetic core and 10(6) turns, operating in limited geometry configuration. Different system noise sources are considered, and a study of the SNR is also included. Finally, some initial Schumann resonance measurements are presented in order to validate the performance of the measurement station, including 1 h length spectra, daily variations of resonance amplitudes and frequencies for the different seasons, and a 3 day spectrogram.
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10. |
- Järlskog, Ida, 1991, et al.
(författare)
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Concentrations of tire wear microplastics and other traffic-derived non-exhaust particles in the road environment
- 2022
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Ingår i: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 170
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Tidskriftsartikel (refereegranskat)abstract
- Tire wear particles (TWP) are assumed to be one of the major sources of microplastic pollution to the environment. However, many of the previously published studies are based on theoretical estimations rather than field measurements. To increase the knowledge regarding actual environmental concentrations, samples were collected and analyzed from different matrices in a rural highway environment to characterize and quantify TWP and other traffic-derived non-exhaust particles. The sampled matrices included road dust (from kerb and in-between wheeltracks), runoff (water and sediment), and air. In addition, airborne deposition was determined in a transect with increasing distance from the road. Two sieved size fractions (2–20 µm and 20–125 µm) were analyzed by automated Scanning Electron Microscopy/Energy Dispersive X-ray spectroscopy (SEM/EDX) single particle analysis and classified with a machine learning algorithm into the following subclasses: TWP, bitumen wear particles (BiWP), road markings, reflecting glass beads, metals, minerals, and biogenic/organic particles. The relative particle number concentrations (%) showed that the runoff contained the highest proportion of TWP (up to 38 %). The share of TWP in kerb samples tended to be higher than BiWP. However, a seasonal increase of BiWP was observed in coarse (20–125 µm) kerb samples during winter, most likely reflecting studded tire use. The concentration of the particle subclasses within airborne PM80-1 decreases with increasing distance from the road, evidencing road traffic as the main emission source. The results confirm that road dust and the surrounding environment contain traffic-derived microplastics in both size fractions. The finer fraction (2–20 µm) dominated (by mass, volume, and number) in all sample matrices. These particles have a high potential to be transported in water and air far away from the source and can contribute to the inhalable particle fraction (PM10) in air. This highlights the importance of including also finer particle fractions in future investigations.
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