| 31. |
- Rämö, Robert, et al.
(författare)
-
Sediment Remediation Using Activated Carbon: Effects of Sorbent Particle Size and Resuspension on Sequestration of Metals and Organic Contaminants.
- 2022
-
Ingår i: Environmental toxicology and chemistry. - : Wiley. - 1552-8618 .- 0730-7268. ; 41:4, s. 1096-1110
-
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.
|
|
| 32. |
- Hetzinger, S., et al.
(författare)
-
High-resolution analysis of trace elements in crustose coralline algae from the North Atlantic and North Pacific by laser ablation ICP-MS
- 2011
-
Ingår i: Palaeogeography Palaeoclimatology Palaeoecology. - 0031-0182. ; 302:1-2, s. 81-94
-
Tidskriftsartikel (refereegranskat)abstract
- We have investigated the trace elemental composition in the skeleta of two specimens of attached-living coralline algae of the species Clathromorphum compactum from the North Atlantic (Newfoundland) and Clathromorphum nereostratum from the North Pacific/Bering Sea region (Amchitka Island, Aleutians). Samples were analyzed using Laser Ablation-Inductively Coupled Plasma Mass Spectrometry (IA-ICP-MS) yielding for the first time continuous individual trace elemental records of up to 69 years in length. The resulting algal Mg/Ca, Sr/Ca, U/Ca, and Ba/Ca ratios are reproducible within individual sample specimens. Algal Mg/Ca ratios were additionally validated by electron microprobe analyses (Amchitka sample). Algal Sr/Ca, U/Ca, and Ba/Ca ratios were compared to algal Mg/Ca ratios, which previously have been shown to reliably record sea surface temperature (SST). Ratios of Sr/Ca from both Clathromorphum species show a strong positive correlation to temperature-dependent Mg/Ca ratios, implying that seawater temperature plays an important role in the incorporation of Sr into algal calcite. Linear Sr/Ca-SST regressions have provided positive, but weaker relationships as compared to Mg/Ca-SST relationships. Both, algal Mg/Ca and Sr/Ca display clear seasonal cycles. Inverse correlations were found between algal Mg/Ca and U/Ca, Ba/Ca, and correlations to SST are weaker than between Mg/Ca, Sr/Ca and SST. This suggests that the incorporation of U and Ba is influenced by other factors aside from temperature. (C) 2010 Elsevier B.V. All rights reserved.
|
|
| 33. |
- Hylén, Astrid, 1991, et al.
(författare)
-
Enhanced benthic nitrous oxide and ammonium production after natural oxygenation of long-term anoxic sediments
- 2022
-
Ingår i: Limnology and Oceanography. - : Wiley. - 0024-3590 .- 1939-5590. ; 67:2
-
Tidskriftsartikel (refereegranskat)abstract
- Coastal and shelf sediments are central in the global nitrogen (N) cycle as important sites for the removal offixed N. However, this ecosystem service can be hampered by ongoing deoxygenation in many coastal areas.Natural reoxygenation could reinstate anoxic sediments as sites wherefixed N is removed efficiently. To investi-gate this further, we studied benthic N cycling in previously long-term anoxic sediments, following a largeintrusion of oxygenated water to the Baltic Sea. During three campaigns in 2016–2018, we measured in situsediment–waterfluxes of ammonium (NHþ4), nitrate (NO�3), oxygen (O2), dissolved inorganic carbon, and NO�3reduction processes using benthic chamber landers. Sediment microprofiles of O2, nitrous oxide (N2O), andhydrogen sulfide were measured in sediment cores. At a permanently oxic station, denitrification to N2was themain NO�3reduction process. Benthic N2O production appeared to be linked to nitrification, although no netN2Ofluxes from the sediment were detected. At newly oxygenated sites, dissimilatory NO�3reduction to NHþ4comprised almost half of the total NO�3reduction. At these stations, the removal offixed N was inefficient dueto high effluxes of NHþ4. Sedimentary N2O production was associated with incomplete denitrification, account-ing for 41–88% of the total denitrification rate. Microprofiling revealed algae aggregates as potential hotspots ofseafloor N2O production. Our results show that transient oxygenation of euxinic systems initiates benthic NO�3reduction, but may not lead to efficient sedimentary removal offixed N. Instead, recycling of N compounds ispromoted, which may accelerate the return to anoxia.
|
|
| 34. |
- Kylander, Malin E., et al.
(författare)
-
Potentials and problems of building detailed dust records using peat archives : An example from Store Mosse (the "Great Bog"), Sweden
- 2016
-
Ingår i: Geochimica et Cosmochimica Acta. - : Elsevier BV. - 0016-7037 .- 1872-9533 .- 0046-564X. ; 190, s. 156-174
-
Tidskriftsartikel (refereegranskat)abstract
- Mineral dust deposition is a process often overlooked in northern mid-latitudes, despite its potential effects on ecosystems. These areas are often peat-rich, providing ample material for the reconstruction of past changes in atmospheric deposition. The highly organic (up to 99% in some cases) matrix of atmospherically fed mires, however, makes studying the actual dust particles (grain size, mineralogy) challenging. Here we explore some of the potentials and problems of using geochemical data from conservative, lithogenic elements (Al, Ga, Rb, Sc, Y, Zr, Th, Ti and REE) to build detailed dust records by using an example from the 8900-yr peat sequence from Store Mosse (the "Great Bog"), which is the largest mire complex in the boreo-nemoral region of southern Sweden. The four dust events recorded at this site were elementally distinct, suggesting different dominant mineral hosts. The oldest and longest event (6385-5300 cal yr BP) sees a clear signal of clay input but with increasing contributions of mica, feldspar and middle-REE- rich phosphate minerals over time. These clays are likely transported from a long-distance source (< 100 km). While dust deposition was reduced during the second event (5300-4370 cal yr BP), this is the most distinct in terms of its source character with [Eu/Eu*] UCC revealing the input of plagioclase feldspar from a local source, possibly active during this stormier period. The third (2380- 2200 cal yr BP) and fourth (1275-1080 cal yr BP) events are much shorter in duration and the presence of clays and heavy minerals is inferred. Elemental mass accumulation rates reflect these changes in mineralogy where the relative importance of the four dust events varies by element. The broad changes in major mineral hosts, grain size, source location and approximated net dust deposition rates observed in the earlier dust events of longer duration agree well with paleoclimatic changes observed in northern Europe. The two most recent dust events are much shorter in duration, which in combination with evidence of their local and regional character, may explain why they have not been seen elsewhere.
|
|
| 35. |
- Maskenskaya, Olga M., et al.
(författare)
-
Source and character of syntaxial hydrothermal calcite veins in Paleoproterozoic crystalline rocks revealed by fine-scale investigations
- 2014
-
Ingår i: Geofluids. - : Wiley. - 1468-8115 .- 1468-8123. ; 14:4, s. 495-511
-
Tidskriftsartikel (refereegranskat)abstract
- Calcite veins in Paleoproterozoic granitoids on the Baltic Shield are the focus of this study. These veins are distinguished by their monomineralic character, unusual thickness and closeness to Neoproterozoic dolerite dykes and therefore have drawn attention. The aim of this study was to define the source of these veins and to unravel their isotopic and chemical nature by carrying out fine-scale studies. Seven calcite veins covering a depth interval of 50-420m below the ground surface and composed of breccias or crack-sealed fillings typically expressing syntaxial growth were sampled and analysed for a variety of physicochemical variables: homogenization temperature (T-h) and salinity of fluid inclusions, and stable isotopes (Sr-87/Sr-86, C-13/C-12, O-18/O-16), trace-element concentrations (Fe, Mn, Mg, Sr, rare earth elements) and cathodoluminescence (CL) of the solid phase. The fluid-inclusion data show that the calcites were precipitated mainly from relatively low-temperature (T-h=73-106 degrees C) brines (13.4-24.5wt.% CaCl2), and the Sr-87/Sr-86 is more radiogenic than expected for Rb-poor minerals precipitated from Neoproterozoic fluids. These features, together with the distribution of C-13 and O-18 values, provide evidence that the calcite veins are not genetic with the nearby Neoproterozoic dolerite dykes, but are of Paleozoic age and were precipitated from warm brines expressing a rather large variability in salinity. Whereas the isotopic and chemical variables express rather constant average values among the individual veins, they vary considerably on fine-scale across individual veins. This has implications for understanding processes causing calcite-rich veins to form and capture trace metals in crystalline bedrock settings.
|
|
| 36. |
- Ranta, E., et al.
(författare)
-
Fluid-rock reactions in the 1.3Ga siderite carbonatite of the GrOnnedal-ika alkaline complex, Southwest Greenland
- 2018
-
Ingår i: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 173:10
-
Tidskriftsartikel (refereegranskat)abstract
- Petrogenetic studies of carbonatites are challenging, because carbonatite mineral assemblages and mineral chemistry typically reflect both variable pressure-temperature conditions during crystallization and fluid-rock interaction caused by magmatic-hydrothermal fluids. However, this complexity results in recognizable alteration textures and trace-element signatures in the mineral archive that can be used to reconstruct the magmatic evolution and fluid-rock interaction history of carbonatites. We present new LA-ICP-MS trace-element data for magnetite, calcite, siderite, and ankerite-dolomite-kutnohorite from the iron-rich carbonatites of the 1.3Ga GrOnnedal-ika alkaline complex, Southwest Greenland. We use these data, in combination with detailed cathodoluminescence imaging, to identify magmatic and secondary geochemical fingerprints preserved in these minerals. The chemical and textural gradients show that a 55m-thick basaltic dike that crosscuts the carbonatite intrusion has acted as the pathway for hydrothermal fluids enriched in F and CO2, which have caused mobilization of the LREEs, Nb, Ta, Ba, Sr, Mn, and P. These fluids reacted with and altered the composition of the surrounding carbonatites up to a distance of 40m from the dike contact and caused formation of magnetite through oxidation of siderite. Our results can be used for discrimination between primary magmatic minerals and later alteration-related assemblages in carbonatites in general, which can lead to a better understanding of how these rare rocks are formed. Our data provide evidence that siderite-bearing ferrocarbonatites can form during late stages of calciocarbonatitic magma evolution.
|
|
| 37. |
- Sonesten, Lars
(författare)
-
Deformiteter hos oligochaeter i Vänern
- 2014
-
Rapport (övrigt vetenskapligt/konstnärligt)abstract
- Bottenlevande slamrörmaskar, oligochaeter, är känsliga miljöindikatorer i alla typerav vatten. I en retrospektiv studie har deformiteter hos oligochaeter från treolika nordliga Vänervikar jämförts under en period med minskad antropogen belastningmed avseende på näringsämnen och olika metaller. Stora mängder av miljöfarligaämnen finns dock lagrade i de sediment som oligochaeterna lever i.Resultaten från undersökningen visar på att de allra grövsta deformitetsformerna,dvs. groteskt förändrade ventrala borst, med tiden generellt sett har minskat i omfattning.Det finns däremot inga tecken på att lättare deformiteter har minskatnämnvärt annat än lokalt. Utöver de skador som noterades på ventrala borst vidtidigare undersökningar så noterades i denna undersökning även att deformiteterhos både dorsala och ventrala borst har tillkommit hos arten Potamothrix hammoniensisi samtliga tre fjärdar. Deformiteterna spänner mellan lättare och mergrava skador, där de lätta dominerar. Liknande skador hos dorsala borst har endastundantagsvis setts i tidigare material från Vänern.Även om förekomsten av de mest grava deformiteterna har minskat, så visar resultatenpå att de lättare skadorna inte har minskat noterbart under den undersöktaperioden annat än på vissa provplatser. Detta skulle kunna tyda på att oligochaeternafortfarande påverkas av upplagrade miljögifter i sedimenten.
|
|
| 38. |
|
|
| 39. |
- Hogmalm, Johan, 1979, et al.
(författare)
-
In situ Rb-Sr and K-Ca dating by LA-ICP-MS/MS: an evaluation of N2O and SF6 as reaction gases
- 2017
-
Ingår i: Journal of Analytical Atomic Spectrometry. - : Royal Society of Chemistry (RSC). - 0267-9477 .- 1364-5544. ; 32:2, s. 305-313
-
Tidskriftsartikel (refereegranskat)abstract
- In situ dating of K-rich minerals, e.g. micas and K-feldspar, by the Rb–Sr isotopic system is a new development made possible by the ICP-MS/MS technique. Online chemical separation of Rb and Sr is possible in an O2-filled reaction cell, wherein a portion of the Sr reacts to SrO+ while simultaneously no RbO+ is formed. O2 reactions provide stable analytical conditions sufficient for precise and accurate determination of Rb/Sr and Sr/Sr isotopic ratios using 80 micron laser ablation spots. However, to date <10% of the Sr reacts with O2 as reaction gas, leaving room for improvement using more potent reaction gases. With a more efficient reactive transfer, it should be possible to obtain similar results with a smaller laser spot size, hence gaining higher spatial resolution. In this study, we have evaluated N2O and SF6 as reaction gases since they have previously been shown to react strongly with Sr+, without affecting Rb+. Analytical conditions, including cell parameters and reaction gas flow rate were optimized while ablating NIST SRM 610. The main reaction product is SrO+ for N2O reaction and SrF+ for SF6 reaction. Both gases show significantly higher reaction product formation compared to O2 with >85% of Sr reacting with N2O and >70% Sr reacting with SF6; Rb does not react with either gas. As a result, the sensitivity for Sr reaction products is ∼10 times higher with N2O and ∼8 times higher with SF6 compared to O2. With these more reactive gases, the error of mica isochron ages, calibrated against a newly developed nano-particulate pressed powder tablet of mica–Mg, is ∼1% using a 50 μm laser spot. Our tests show that both N2O and SF6 form interfering reaction products, e.g., SrOH (N2O), SiF3 and TiF3 (SF6) that are difficult to handle using single mass spectrometer instruments, but which can be overcome using MS/MS. Using SF6 combined with H2, it is possible to measure 40Ca+ as 40Ca19F+, free from interference of 40Ar+ and 40K+. This facilitates the dating of micas by the K–Ca isotopic system; we present the first in situ K–Ca age determination.
|
|
| 40. |
- Konrad-Schmolke, Matthias, 1970, et al.
(författare)
-
Discrimination of thermodynamic and kinetic contributions to the heavy rare earth element patterns in metamorphic garnet
- 2022
-
Ingår i: Journal of Metamorphic Geology. - : Wiley. - 0263-4929 .- 1525-1314. ; 41:4, s. 465-90
-
Tidskriftsartikel (refereegranskat)abstract
- Variations of rare earth element (REE) concentrations in metamorphic garnet are an important source of information of geodynamic and geochemical processes in the deeper Earth. In order to extract this information, the thermodynamic equilibrium and kinetic contributions of the REE uptake in garnet must be distinguished and quantified. Utilizing high-resolution trace element and μ-Raman mapping together with combined thermodynamic–geochemical–diffusion models, we demonstrate that the equilibrium and kinetic aspects of the REE uptake in metamorphic garnet can be discriminated by interpreting 2D trace element mapping in a single sample. The heavy (H) REE (Tb to Lu) zoning in the investigated garnet from a high-pressure blueschist comprises an inner part with an overall decrease from core to inner rim, followed by a concentric zone of HREE enrichment and a drastic HREE decrease towards the outermost rim. The central peak in the garnet core decreases in intensity with decreasing atomic number of the REE. The broad overall shape of this pattern resembles those often observed in metamorphic garnet from different rock types and tectonic settings. Superimposed on this trend is a concentric pattern of minor recurring fluctuations in the HREE concentrations with at least six regularly spaced sets of peaks and troughs along the entire garnet radius. Comparison of the observed inclusion suite, the trace element maps and thermodynamic–geochemical models show that the inner part with decreasing HREE concentrations results from fractional garnet growth in an unchanged mineral assemblage, whereas the REE enrichment zone is caused by the breakdown of titanite. We suggest that the width of the central peak is controlled by the bulk permeability of the interconnected transport matrix and the fraction of matrix minerals that the garnet equilibrates with. The superimposed REE fluctuations result from changing element transport properties of the host rock and mark recurring changes from equilibrium REE uptake to transport-limited REE uptake in garnet. Such fluctuating element transport properties can be best explained by pulse-like fluid fluxes that rhythmically change the interconnectivity of the intercrystalline transport matrix. Increasing numbers of published spatially highly resolved REE analyses show that such trace element fluctuations are common in metamorphic garnet indicating that recurring changes in rock permeabilities due to pulsed fluid fluxes are a common phenomenon during metamorphism.
|
|
