| 1. |
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| 2. |
- Bolin, Marie, et al.
(författare)
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Prediction of Preeclampsia by Combining Serum Histidine-Rich Glycoprotein and Uterine Artery Doppler
- 2012
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Ingår i: American Journal of Hypertension. - : Oxford University Press (OUP). - 0895-7061 .- 1941-7225. ; 25:12, s. 1305-1310
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Tidskriftsartikel (refereegranskat)abstract
- BackgroundPreeclampsia is associated with both maternal and perinatal morbidity and mortality. Histidine-rich glycoprotein (HRG) is a protein interacting with angiogenesis, coagulation, and inflammatory responses, processes known to be altered in preeclamptic pregnancies. Significantly lower levels of HRG have been demonstrated as early as in the first trimester in women later developing preeclampsia compared with normal pregnancies. The aim of this study was to investigate whether the combination of HRG and uterine artery Doppler ultrasonography can be used as a predictor of preeclampsia.MethodsA total of 175 women were randomly selected from a case-control study; 86 women had an uncomplicated pregnancy and 89 women later developed preeclampsia. Blood samples and pulsatility index (PI) were obtained from both cases and controls in gestational week 14.ResultsHRG levels were significantly lower in women who developed preterm preeclampsia compared with controls, but not for women developing preeclampsia in general. PI was significantly higher in the preeclampsia group compared with controls, especially in preterm preeclampsia. The combination of HRG and PI revealed a sensitivity of 91% and a specificity of 62% for preterm preeclampsia.ConclusionsThe combination of HRG and uterine artery Doppler may predict preterm preeclampsia in early pregnancy.
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| 3. |
- Celma, Alberto, et al.
(författare)
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Analysis of polycyclic aromatic hydrocarbons (PAHs) and their derivatives in biochar treated stormwater
- 2023
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Ingår i: MethodsX. - 2215-0161. ; 10
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Tidskriftsartikel (refereegranskat)abstract
- Polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs (oxy-PAHs) and nitrogen heterocyclic polycyclic aromatic compounds (N-PACs) are persistent and semi-volatile organic compounds primarily formed due to incomplete combustion of organic material or, in the case of the derivatives, through transformation reactions of PAHs. Their presence in the environment is ubiquitous and many of them have been proven carcinogenic, teratogenic, and mutagenic. These toxic pollutants can therefore pose a threat to both ecosystem and human health and urges for remediation strategies for PAHs and derivatives from water bodies. Biochar is a carbon-rich material resulting from the pyrolysis of biomass resulting in a very porous matter with high surface area for an enhanced interaction with chemicals. This makes biochar a promising alternative for filtering micropollutants from contaminated aquatic bodies. In this work, a previously developed and validated methodology for the analysis of PAHs, oxy-PAHs and N-PACs in surface water samples was adapted for its utilization in biochar treated stormwater with special emphasis on scaling down the solid-phase extraction as well as including an additional filtering step for the removal of particulate matter in the media. & BULL; Optimized extraction method for PAHs, oxy-PAHs and N-PACs from stormwater treated with biochar. & BULL; Biochar strongly impacts the stormwater matrix and, therefore, additional steps are required in the extraction methodology. & BULL; Solid-phase extraction combined with GC-MS have been used to analyse PAHs, oxy-PAHs and N-PACs in stormwater treated with biochar.
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| 4. |
- Dahlberg, Anna-Karin, et al.
(författare)
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Capping fiberbank sediments to reduce persistent organic pollutants (POPs) fluxes : A large-scale laboratory column experiment
- 2023
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Ingår i: Environmental Pollution. - : Elsevier BV. - 0269-7491 .- 1873-6424. ; 333
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Tidskriftsartikel (refereegranskat)abstract
- Deposits of contaminated wood fiber waste (fiberbanks), originating from sawmills and pulp and paper industries, have been found in the aquatic environment in boreal countries. In-situ isolation capping has been proposed as a remediation solution because it has the potential to prevent dispersal of persistent organic pollutants (POPs) from this type of sediment. However, knowledge about the performance of such caps when placed on very soft (un-consolidated), gaseous organic rich sediment is scarce. We investigated the effectiveness of conventional in-situ capping to limit POPs fluxes to the water column from contaminated fibrous sediments that produce gas. A controlled, large-scale laboratory column (40 cm diameter, 2 m height) experiment was performed over 8 months to study changes in sediment-to-water fluxes of POPs and particle resuspension before and after capping the sediment with crushed stones (& GE;4 mm grain size). Two different cap thicknesses were tested (20 and 45 cm) on two types of fiberbank sediment with different fiber type composition. Results showed that capping fiberbank sediment with a 45 cm gravel cap reduced the sediment-to-water flux by 91-95% for p,p'-DDD, o,p'-DDD, by 39-82% for CB-101, CB-118, CB-138, CB-153, CB-180 and by 12-18% for HCB, whereas for less hydrophobic PCBs, capping was largely ineffective (i.e. CB-28 and CB-52). Although cap application caused particle resus-pension, the long-term effect of the cap was reduced particle resuspension. On the other hand, substantial sediment consolidation released large volumes of contaminated pore water into the overlying water body. Importantly, both sediment types produced large amount of gas, observed as gas voids forming inside the sediment and gas ebullition events, which increased pore water advection and affected the structural integrity of the cap. This may limit the practical applicability of this method on fiberbank sediments.
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| 5. |
- Dahlberg, Anna-Karin, et al.
(författare)
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Dispersal of persistent organic pollutants from fiber-contaminated sediments : biotic and abiotic pathways
- 2021
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Ingår i: Journal of Soils and Sediments. - : Springer Science and Business Media LLC. - 1439-0108 .- 1614-7480. ; 21:4, s. 1852-1865
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Tidskriftsartikel (refereegranskat)abstract
- PurposeNumerous sites contaminated with fiber emissions from pulp and paper industries are found in coastal areas of the Baltic Sea, but there is limited knowledge about the magnitude of dispersal of persistent organic pollutants (POPs) from these anthropogenic, organic-rich sediments called fiberbanks. The aim of this study was to quantify and compare different POP dispersal pathways from such fiberbanks. Dispersal mechanisms studied included abiotic and biotic routes (dissolved in water, particle-bound, and bioaccumulation).Materials and methodsContaminated fibrous sediments located in Ångermanälven River estuary in north-eastern Sweden were studied in sediment types representing different fiber content (i.e., fiberbanks, fiber-rich sediments, and less fiber impacted sediments). Sediment-to-water fluxes of dissolved contaminants (polychlorinated biphenyls (PCBs), hexachlorobenzene (HCB), and dichlorodiphenyltrichloroethane (DDT)) were measured in situ using benthic flux chambers. Particle resuspension was measured by sampling bottom water, before and after disturbing the sediment surface. Benthic biota was collected to determine the body burden of contaminants and to determine biota-pore water accumulation factors (BAFPW) and biota-sediment accumulation factors (BSAFs). In addition, concentrations of dissolved POPs in the water column were measured in field using passive samplers. Instrumental analysis was performed using gas chromatography coupled to a triple quadrupole mass spectrometer (GC-MS/MS).Results and discussionThe flux of dissolved Σ20PCBs was approximately two times higher from one of the investigated fiberbanks (3.4 ng m− 2 day− 1) compared to the other. The average particle burden of PCBs was also higher at this fiberbank after artificial disturbance (15 ng g−1 particle), which indicates that larger amounts of contaminants are likely to disperse via particle resuspension from this site compared to the other fiberbank (4.8 ng g− 1 particle). The difference might be associated with a layer of recently settled minerogenic material that covers one of the fiberbanks, which probably functions as a protective barrier. The lack of benthic biota implies that contaminant release by bioturbation is negligible in the studied fiberbanks. However, benthic biota from fiber-rich sediment showed bioaccumulation and biomagnification of contaminants.ConclusionsThe importance of diffusive flux from fiberbanks under undisturbed conditions became apparent when the different dispersal pathways were quantified. However, no dispersal pathway could be judged as irrelevant, since even under undisturbed conditions, advective particle transport was significant. Additionally, the uptake by biota and trophic transfer can be considerable. Quantification of dispersal routes and understanding of the relative importance of various pathways is critical for proper risk assessment and management of contaminated sediments.
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| 6. |
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| 7. |
- Dahlberg, Anna-Karin, 1982-, et al.
(författare)
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Persistent organic pollutants in wood fiber–contaminated sediments from the Baltic Sea
- 2020
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Ingår i: Journal of Soils and Sediments. - : Springer Science and Business Media LLC. - 1439-0108 .- 1614-7480. ; 20:5, s. 2471-2483
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Tidskriftsartikel (refereegranskat)abstract
- Many coastal areas in the Baltic Sea are contaminated with wood fiber and pollutants from pulp and paper industries. These anthropogenic, organic-rich, sediments (fiberbanks) have not been characterized and knowledge about their role as secondary sources for dispersal of persistent organic pollutants (POPs) is limited. Hence, the aim of this study was to elucidate the fate of POPs and the relationships between sorption (KD and KTOC), sediment type, and compound hydrophobicity (KOW) in fiber-contaminated sediments.
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| 8. |
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| 9. |
- Goransson, Gunnel, et al.
(författare)
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Assessing the Risk of Contaminant Dispersion From Fibrous Sediments of Industrial Origin
- 2021
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Ingår i: Frontiers in Marine Science. - : Frontiers Media S.A.. - 2296-7745. ; 8
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Tidskriftsartikel (refereegranskat)abstract
- Unregulated discharges of wastewater from pulp and paper factories resulted in the formation of relatively thick organic (cellulose) rich sediments in shallow waters along the Swedish coast. These deposits are known as fiberbanks and are contaminated by persistent organic pollutants (POPs), metals and methylmercury, which can be dispersed by diffusion and advective processes coupled to propeller wash, high river discharges, strong wind waves and submarine landslides. Based on a case study of polychlorinated biphenyls (PCBs), one group of prevalent POPs in the fiberbanks, we present a probabilistic approach to estimate the potential risk of dispersion of fiberbank contaminants. The approach allows for estimation of the dispersal pathways that dominates the risk within a given time and provides more insight about the significance of various dispersion processes. We show that it is highly likely that chemical diffusion and advection triggered by ship-induced resuspension will disperse PCBs (sum of seven congeners; sigma 7PCB) above a threshold level for environmental impact, while the likelihood of river and wind-wave generated resuspension dispersion pathways are lower (similar to 20%, respectively). We further show that there is approximately 5% likelihood that a submarine landslide will disperse sigma 7PCB above the threshold level. The study implies that the governing parameters for risk assessment specifically should include reliable data on contaminant concentration, water depth above the fiberbank, estimation of concerned fiberbank areas, time duration of erosive fluid flows and measured diffusion. The approach provides insight into the importance of various dispersion processes. We suggest that it can be applied to support risk assessment, especially when there are limited available data and/or knowledge about the system under study.
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| 10. |
- Sha, Bo, et al.
(författare)
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Fluorotelomer alcohols (FTOHs), brominated flame retardants (BFRs), organophosphorus flame retardants (OPFRs) and cyclic volatile methylsiloxanes (cVMSs) in indoor air from occupational and home environments
- 2018
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Ingår i: Environmental Pollution. - : Elsevier BV. - 0269-7491 .- 1873-6424. ; 241, s. 319-330
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Tidskriftsartikel (refereegranskat)abstract
- Indoor air samples were collected from private homes and various occupational indoor environments using passive air sampler and analysed for fluorotelomer alcohols (FTOHs), brominated flame retardants (BFRs), organophosphorus flame retardants (OPFRs) and cyclic volatile methyl siloxanes (cVMSs). The aim was to investigate their occurrence in indoor air, factors that may affect their presence and human daily exposure dose (DED) via inhalation. In general, levels of cVMSs were 3-4 orders of magnitude greater than the other compound classes. OPFRs concentration was found significantly higher than BFRs in indoor air. The most abundant compounds in each chemical class were 8:2 FTOH, 2,4,6-TBP, TNBP and TCEP and decamethylcyclopentasiloxane (D5). Home samples contained higher level of FTOHs, BFRs and cVMSs than occupational environments, whereas concentration of OPFRs in office samples were higher. BFRs concentrations were significantly correlated with building age and with the number of electronic/ electrical devices at the sampling sites. Moreover, significantly lower levels of FTOHs and cVMSs were observed in rooms with forced-ventilation system. Estimated DED via inhalation was significantly higher at home than in office and the total DED was on average 3-5 orders of magnitude lower than the reference value. (C) 2018 Elsevier Ltd. All rights reserved.
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| 11. |
- Volchko, Yevheniya, 1979, et al.
(författare)
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Assessing costs and benefits of improved soil quality management in remediation projects : A study of an urban site contaminated with PAH and metals
- 2020
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Ingår i: Science of the Total Environment. - : Elsevier. - 0048-9697 .- 1879-1026. ; 707
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Tidskriftsartikel (refereegranskat)abstract
- Contaminants in the soil may threaten soil functions (SFs) and, in turn, hinder the delivery of ecosystem services (ES). A framework for ecological risk assessments (ERAs) within the APPLICERA - APPLICable site-specific Environmental Risk Assessment research project promotes assessments that consider other soil quality parameters than only contaminant concentrations. The developed framework is: (i) able to differentiate the effects of contamination on SFs from the effects of other soil qualities essential for soil biota; and (ii) provides a robust basis for improved soil quality management in remediation projects. This study evaluates the socio-economic consequences of remediation alternatives stemming from a Tier 1 ERA that focusses on total contaminant concentrations and soil quality standards and a detailed, site-specific Tier 3 Triad approach that is based on the APPLICERA framework. The present study demonstrates how Tier 1 and Tier 3 ERAs differ in terms of the socio-economic consequences of their remediation actions, as well as presents a novel method for the semi-quantitative assessment of on-site ES. Although the presented Tier 3 ERA is more expensive and time-consuming than the more traditional Tier 1 ERA approach, it has the potential to lower the costs of remediation actions, decrease greenhouse gas emissions, reduce other environmental impacts, and minimise socio-economic losses. Furthermore, the remediation actions stemming from the Tier 3 ERA were predicted to exert far less negative ES effects than the actions proposed based on the results of the Tier 1 ERA.
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| 12. |
- Wiberg, Karin, et al.
(författare)
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Spatial distribution of legacy pesticides in river sediment from the Republic of Moldova
- 2021
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Ingår i: Chemosphere. - : Elsevier BV. - 0045-6535 .- 1879-1298. ; 279
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Tidskriftsartikel (refereegranskat)abstract
- Historical use of organochlorine pesticides (OCPs) in the Republic of Moldova could pose a potential risk for the aquatic environment due to the persistence, bioaccumulation and toxic properties of these environmental pollutants. However, knowledge on environmental concentrations of legacy OCPs in Moldova is limited. In this study, surface sediment from the two main rivers; Dniester (8 sites, n = 15) and Prut (6 sites, n = 12), and two tributary rivers; Bic (11 sites, n = 11) and Raut (6 sites, n = 6), were collected during 2017-2018 and analyzed for hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs) and their transformation products (DDDs and DDEs) using gas chromatography coupled to mass spectrometry (GC-MS/MS). Sediment concentrations of Sigma 6DDX (1.9-140 ng g(-1) dry weight (dw)) and Sigma(4)HCHs (n.d-2.5 ng g(-1) dw) were found. In the big rivers, the average Sigma 6DDX concentration (18 ng g(-1) dw) were 35 times higher than Sigma(4)HCHs (0.51 ng g(-1) dw). Whereas, in the small rivers the average Sigma 6DDX concentration (32 ng g(-1) dw) was approximately 41 times higher than Sigma(4)HCHs (0.77 ng g(-1) dw). Compared to previous studies from Eastern Europe, the sediment levels were generally similar as found in Moldova's neighboring countries (Romania and Ukraine). Overall, the contamination profile indicates long-term ageing of OCPs used in the past in the agricultural sector. Less than half of the sites (45%) had levels that pose a potential risk for benthic organisms. Hence, further work is needed to determine the bioaccumulation of OCPs in the aquatic food web in this region and the associated risks to ecosystems and human health.
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| 13. |
- Ahrens, Lutz, et al.
(författare)
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Analysis of per- and polyfluoroalkyl substances (PFASs) and phenolic compounds in Swedish rivers over four different seasons
- 2018
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- Syftet med denna studie var att undersöka miljökoncentrationer, sammansättning, säsongsvariationoch flöden av 28 PFAS-substanser och 10 fenolära ämnen i 10 svenska vattendrag över fyra olikaårstider (oktober 2016, januari 2017, april 2017 och juli 2017). Totalt detekterades 7 av 28 PFASämneni relativt låga nivåer (i genomsnitt 3,2 ng per liter för Σ28PFAS) i flodvatten (n = 40).Koncentrationerna av de fenolära föreningarna var generellt högre (genomsnittshalt 230 ng per literför summan av alla fenoler som mättes; n = 38). Detektionsfrekvensen var dock låg (i genomsnitt50%), vilket resulterade i låga mediankoncentrationer för summahalten (0 ng per liter). Dedominerande PFAS-substanserna var perfluorbutansulfonsyra (PFBS, 38% av Σ28PFAS),perfluoroktansyra (PFOA, 21%) och perfluoroktansulfonsyra (PFOS (grenad), 8,9%) medan dedominerande fenolära föreningarna var 4-nonylfenol (4-NP, 67%), 4-tert-nonylfenol-dietoxilat (4-NP-EO2, 20%) och 2,4,6-tribromfenol (TBP, 10%). Koncentrationerna av PFAS och fenolföreningaruppvisade ingen säsongsvariation under de fyra undersökta årstiderna, vilket indikerar ett relativtstabilt flöde av dessa två ämnesklasser till vattendragen. De uppmätta PFAS-koncentrationerna varinte relaterade till koncentrationerna av fenolära föreningarna, vilket indikerar olika källor för de tvåämnesklasserna. Flödena för totalhalterna uppskattades till 220 g per dag (81 kg per år) för Σ28PFAS,och >70 gånger högre för de fenolära ämnena med totalflöden på 16000 g per dag (5700 kg per år).Miljökvalitetsstandarden för ett årligt genomsnitt (AA-EQS) som anges i EU: s ramdirektiv förvatten (WFD) överskreds för 33% (n = 13) av vattenproverna för summan av linjära och grenadePFOS och för 13% (n = 5) av för 4-NP. Detta indikerar att halterna av PFOS och 4-NP utgör enpotentiell risk för vattenmiljön. AA-EQS för 4-oktylfenol (4-OP) och pentaklorfenol (PCP)överskreds inte i något fall.vatten (WFD) överskreds för 33% (n = 13) av vattenproverna för summan av linjära och grenadePFOS och för 13% (n = 5) av för 4-NP. Detta indikerar att halterna av PFOS och 4-NP utgör enpotentiell risk för vattenmiljön. AA-EQS för 4-oktylfenol (4-OP) och pentaklorfenol (PCP)överskreds inte i något fall.
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| 14. |
- Ahrens, Lutz, et al.
(författare)
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Analysis of per- and polyfluoroalkyl substances (PFASs) and phenolic compounds in Swedish rivers over four different seasons
- 2018
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- Per- and polyfluoroalkyl substances (PFASs) and phenolic compounds are emerging organic pollutants characterized by their persistency, bioaccumulation and toxicity potential. In this study, 28 PFASs and 10 phenolic compounds were investigated in 10 Swedish rivers over four different seasons (October 2016, January 2017, April 2017 and July 2017). The objective was to investigate the levels, composition profiles, sesonal trends and fluxes for both compound classes. In total, 7 out of 28 PFASs and 9 out of 10 phenolic compounds were detected in surface water from the 10 rivers. The average concentration in all samples was 3.2 ng L-1 for ∑28PFASs (median 2.4 ng L-1, n = 40), while 230 ng L-1 for the sum of the phenolic compounds (median 0 ng L-1, n = 38). Highest average ∑28PFAS concentrations were found in Rönneån with 10 ng L-1 (median 11 ng L-1), followed by Norrström with 9.0 ng L-1 (median 9.1 ng L-1), whereas no PFASs were detected in Umeå älv and Ångermanälven. On the other hand, highest average of the sum of the phenolic compound concentrations were found in Nyköpingsån with 1500 ng L-1 (median 57 ng L-1), while for the other rivers the average ranged between 50 ng L-1 and 140 ng L-1, except for Emån where TBP was only detected in one sample with 0.33 ng L-1. This indicates that PFASs and phenolic compounds origin from different sources. The dominant PFASs were perfluorobutane sulfonic acid (PFBS, 38 % of the ∑28PFASs), perfluorooctanoic acid (PFOA, 21 %), and perfluorooctane sulfonic acid (PFOS (branched), 8.9 %), while the dominant phenolic compounds were 4nonylphenol (4-NP, 67 %), 4-tert-nonylphenol-diethoxylate (4-NP-EO2, 20 %), and 2,4,6tribromophenol (TBP, 10 %). The concentrations of PFASs and phenolic compounds were relatively constant during the four investigated seasons which indicates a relatively steady input of these two compound classes into the river systems. The daily fluxes of Σ28PFAS was estimated to be in total 220 g d-1 (81 kg year-1), whereas the daily fluxes of phenolic compounds was estimated to be 16000 g d-1 (5700 kg year-1) for all 10 investigated rivers. The Annual Average Environmental Quality Standard (AA-EQS) of the EU Water Framework Directive (WFD) was exceeded in 33% (n = 13) of the surface water samples for the sum of linear and branched PFOS and in 13% (n = 5) of the surface water samples for 4NP. This indicates that there is a potential risk for the aquatic environment. The AA-EQS of 4-octylphenol (4-OP) and pentachlorophenol (PCP) was not exceeded in any surface water sample.
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| 15. |
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| 16. |
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| 17. |
- Ahrens, Lutz, et al.
(författare)
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Screening av perfluoralkylerade ämnen och flamskyddsmedel i svenska vattendrag
- 2014
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- Syftet med projektet var att studera förekomst av perfluoralkylerade ämnen (PFASs) samt relativt nya flamskyddsmedel (FRs) i svenska vattendrag. Vi provtog på 44 platser (totalt 41 vattendrag) och bestämde innehållet av PFASs (alla platser) och FRs (25 platser). Av de 12 utvalda FRs, kunde 3 kvantifieras. TCIPP var det klart dominerade ämnet med en halt på upp till 3900 ng L-1 (Fyrisån). 2,4,6-TBP uppvisade högre halter i åar i södra Sverige. Vattendragen med de högsta av σFRs var Fyrisån och Norrström. Den totala belastningen på östersjön av σFRs uppskattades till 38 kg dag-1, där ångermanlandsälven och Norrström stod för de största bidragen. Det ska noteras att i dessa belastningssiffror ingår inte äldre FRs med omfattande historisk användning, t.ex. PBDE. Totalt 13 av 25 de analyserade PFASs kunde kvantifieras. Medelvärdet av σPFASs i alla vattendrag var 9,5 ng L-1, och de högsta medelhalterna uppmättes för PFBS och PFHxS (~2 ng L-1). Det sammanlagda utflödet av σPFASs uppgick till 3,2 kg dag-1. PFOS överskred miljökvalitetsnormen på 0,65 ng L-1 (årligt medelvärde; AA-EQS; 2013/39/EU) på 12 av 44 platser.Den här fältstudien baseras på en provtagningskampanj med ögonblicksprovtagning, och därför ska alla rapporterade värden tolkas med försiktighet. Verifikation av höga resultat och mer detaljerade studier på platser med förhöjda värden rekommenderas. Studien pekar också på att uppströmsmätningar är nödvändiga för att finna viktiga föroreningskällor.
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| 18. |
- Ahrens,, Lutz, et al.
(författare)
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Screening av PFAS i grund- och ytvatten
- 2016
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- Levels of 26 per- and polyfluoroalkyl substances (PFASs) were measured in 502 water samples originat-ing from Swedish groundwater, surface water, sewage treatment plant (STP) effluents and landfill leachates. In drinking water source areas, the average Σ26PFAS concentration was 8.4 ng L-1. The national drinking water guideline value of 90 ng L-1 for Σ7PFASs was exceeded in 2% of these samples. In water not used for drinking water, Σ26PFASs average concentration was 142 ng L-1. PFOS concentra-tions exceeded the Annual Average Environmental Quality Standard (AA-EQS) of the EU Water Frame-work Directive in 42% of the surface water samples. Among the different water categories, the landfill leachates had the highest average concentration of Σ26PFAS with 487 ng L-1, followed by surface water (average 112 ng L-1), groundwater (49 ng L-1), STP effluents (35 ng L-1) and background screening lakes (3.4 ng L-1). The composition profile of the PFASs differed between the types of waters showing an even distribution of ΣPFCAs, ΣPFSAs and ΣPFAS precursors in groundwater, whereas in all other water categories, ΣPFCAs were dominant. As FOSA, PFNA, PFDA, and 6:2 FTSA were frequently detected in drinking water source areas (constituted 20%, 7.3%, 5.9%, and 4.4% of the Σ26PFASs, respectively), it is reasonable to consider the inclusion of these in the Swedish drinking water guideline.
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| 19. |
- Ahrens, Lutz, et al.
(författare)
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Screening of perfluoroalkyl substances and organic flame retardants in Swedish Rivers : Screening av perfluoralkylerade ämnen och flamskyddsmedel i svenska vattendrag
- 2013
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- The occurrence and effects of ubiquitously present persistent organic pollutants (POPs) in the environment is one of the challenges the society is facing today. Two categories of chemicals that have gained increased public attention during the last decades are organic flame retardants (FRs) and perfluoroalkyl substances (PFASs). Many representatives from these compound groups have bioaccumulative, persistent and toxic properties. This has led to a ban of some of these compounds based on international agreements.FRs and PFASs end up in surface waters and sometimes also in ground water due to their widespread distribution, disinclination of getting removed at wastewater treatment plants (WWTPs), and persistence. However, the knowledge of the occurrence, fate, and effect in the environment of FRs and PFASs is still in great need of research, especially for recently introduced compounds (such as novel FRs). The objective of this project was to provide a snapshot of the current pollution situation of PFASs and selected novel FRs in Swedish surface waters. We sampled at 44 sites (representing 41 rivers and streams) along the whole coastline of Sweden and analysed their content of PFASs (all sites) and FRs (25 sites representing 23 rivers).Among the 12 target FRs, 3 could be quantified (2,4,6-TBP, TCIPP, and TPHP). TCIPP was the predominant compound with a level up to 3 900 ng L-1. The 2,4,6-TBP showed higher levels in southern rivers. The river with highest levels of ΣFRs was Fyrisån, and the total riverine input of the targeted FRs into the Baltic Sea was estimated to 38 kg day-1 with Ångermanlandsälven and Norrström as major contributors. It should be noted that these values only include the targeted, relatively novel FRs, while historically more important FRs such as the polybrominated diphenyl ethers (PBDEs), are not included.In total 13 PFASs were detected (PFBA, PFHxA, PFHpA, PFOA, PFNA, PFDA, PFUnDA, PFDoDA, PFTeDA, FOSA, PFBS, PFHxS, PFOS) among the 25 target compounds. The mean ΣPFAS level of all sampled rivers was 9.5 ng L-1 and the median 4.2 ng L-1, and the highest mean values were found for PFBS and PFHxS (~2 ng L-1 for each compound). Streams in the north (e.g. Alterälven, Öre älv, Gide älv, Lögde älv and Ljungan) showed generally higher fractions of the longer chained perfluoroalkyl carboxylic acids (PFCAs; i.e. PFNA, PFDA, PFUnDA, PFDoDA, PFTeDA) whereas in the south the fractions of PFHpA and PFOA were higher. The total riverine input of all PFASs into recipient seas was estimated to 3.2 kg day-1 (1150 kg yr-1).PFOS exceeded the annual average Environmental Quality Standard (AA-EQS; 2013/39/EU) of 0.65 ng L-1 at 12 of 44 sampling sites, which are located in all parts of Sweden (Ume älv at Gubböle, Ångermanälven, Delångersån, Fyrisån, Norrström, Nyköpingsån, Emån, Lyckebyån, Rönneån, Nissan, Viskan and Göta älv at Alelyckan).As this study was a one-time grab sampling campaign for screening purposes, all values should be interpreted with care. A screening study like the current may, however, reveal hot spots. Verification and more detailed studies over a longer time period are recommended for sites with elevated levels. Our study also suggests that upstream monitoring is necessary to reveal important pollution sources.
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| 20. |
- Ahrens, Lutz, et al.
(författare)
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Screening of PFASs in groundwater and surface water
- 2016
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- Per- and polyfluoroalkyl substances (PFASs) are emerging organic pollutants characterized by their persistency, and bioaccumulation and toxicity potential. In this study, 26 PFASs were screened in 502 water samples originating from Swedish groundwater, surface water, sewage treatment plant (STP) effluents and landfill leachates. The objectives were to establish baseline concentrations of PFASs in the aquatic environment, to screen for potential sources, and to compare PFAS concentrations with guideline values for estimation of potential effects on the ecosystem and human health. In drinking water source areas, the average ∑26PFAS concentration was 8.4 ng L-1 with a median value of 0.6 ng L-1 (n = 172). The drinking water guideline value of 90 ng L-1 for ∑7PFASs (PFPeA, PFHxA, PFHpA, PFOA, PFBS, PFHxS, PFOS) established by the Swedish National Food Agency was exceeded in 4 samples (2% of the total number of samples in this category). In water not used for drinking water, ∑26PFASs concentrations were on average 142 ng L-1 (median 5.4 ng L-1). The high average PFAS concentrations can be explained by the fact that some samples showed extremely high PFAS concentrations with a maximum ∑26PFASs value of 12 900 ng L-1. In surface water, PFOS concentrations exceeded the annual average Environmental Quality Standard (AA-EQS) of the EU Water Framework Directive (WFD) in 42% of the samples. Among the different water categories, the landfill leachates had the highest average concentration of ∑26PFAS with 487 ng L-1 (median 435 ng L-1, n = 10), followed by surface water (average 112 ng L-1, median 4.1 ng L-1, n = 285), groundwater (average 49 ng L-1, median 0.4 ng L-1, n = 164), STP effluents (average 35 ng L-1, median 26 ng L-1; n = 13) and background screening lakes (remote lakes; average 3.4 ng L-1, median 1.4 ng L-1, n = 10). The composition profile of the PFASs differed between the types of waters showing an even distribution of ∑PFCAs, ∑PFSAs and ∑PFAS precursors in groundwater, whereas in all other water categories (surface water, background lakes, STP effluents and landfill leachates), ∑PFCAs were dominant. As FOSA, PFNA, PFDA, and 6:2 FTSA were frequently detected in drinking water source areas (constituted 20%, 7.3%, 5.9%, and 4.4% of the ∑26PFASs, respectively), it is reasonable to consider the inclusion of these in the Swedish drinking water guideline.
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- Ahrens, Lutz, et al.
(författare)
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The relevant role of ion mobility separation in LC-HRMS based screening strategies for contaminants of emerging concern in the aquatic environment
- 2021
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Ingår i: Chemosphere. - : Elsevier BV. - 0045-6535 .- 1879-1298. ; 280
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Tidskriftsartikel (refereegranskat)abstract
- Ion mobility separation (IMS) coupled to high resolution mass spectrometry (IMS-HRMS) is a promising technique for (non-)target/suspect analysis of micropollutants in complex matrices. IMS separates ionized compounds based on their charge, shape and size facilitating the removal of co-eluting isomeric/isobaric species. Additionally, IMS data can be translated into collision cross-section (CCS) values, which can be used to increase the identification reliability. However, IMS-HRMS for the screening of contaminants of emerging concern (CECs) have been scarcely explored. In this study, the role of IMS-HRMS for the identification of CECs in complex matrices is highlighted, with emphasis on when and with which purpose is of use. The utilization of IMS can result in much cleaner mass spectra, which considerably facilitates data interpretation and the obtaining of reliable identifications. Furthermore, the robustness of IMS measurements across matrices permits the use of CCS as an additional relevant parameter during the identification step even when reference standards are not available. Moreover, an effect on the number of true and false identifications could be demonstrated by including IMS restrictions within the identification workflow. Data shown in this work is of special interest for environmental researchers dealing with the detection of CECs with state-of-the-art IMS-HRMS instruments.
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