| 1. |
- Schönlau, Christine, 1986-, et al.
(författare)
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Effect-Directed Analysis of Ah Receptor-Mediated Potencies in Microplastics Deployed in a Remote Tropical Marine Environment
- 2019
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Ingår i: Frontiers in Environmental Science. - : Frontiers Media S.A.. - 2296-665X. ; 7
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Tidskriftsartikel (refereegranskat)abstract
- To facilitate the study of potential harmful compounds sorbed to microplastics, an effect-directed analysis using the DR CALUX® assay as screening tool for Aryl hydrocarbon receptor (AhR)-active compounds in extracts of marine deployed microplastics and chemical analysis of hydrophobic organic compounds (HOCs) was conducted. Pellets of three plastic polymers [low-density polyethylene (LDPE), high-density polyethylene (HDPE) and high-impact polystyrene (HIPS)] were deployed at Heron Island in the Great Barrier Reef, Australia, for up to 8 months. Detected AhR-mediated potencies (bio-TEQs) of extracted plastic pellets ranged from 15 to 100 pg/g. Contributions of target HOCs to the overall bioactivities were negligible. To identify the major contributors, remaining plastic pellets were used for fractionation with a gas chromatography (GC) fractionation platform featuring parallel mass spectrometric (MS) detection. The bioassay analysis showed two bioactive fractions of each polymer with bio-TEQs ranging from 5.7 to 14 pg/g. High resolution MS was used in order to identify bioactive compounds in the fractions. No AhR agonists could be identified in fractions of HDPE or LDPE. Via a multivariate statistical approach the polystyrene (PS) trimer 1e- Phenyl-4e-(1- phenylethyl)-tetralin was identified in fractions of HIPS and in fractions of the blank polymer of HIPS.
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| 2. |
- De Silva, Amila O., et al.
(författare)
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PFAS Exposure Pathways for Humans and Wildlife : A Synthesis of Current Knowledge and Key Gaps in Understanding
- 2021
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Ingår i: Environmental Toxicology and Chemistry. - : Pergamon Press. - 0730-7268 .- 1552-8618. ; 40:3, s. 631-657
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Forskningsöversikt (refereegranskat)abstract
- Here we synthesize current understanding of the magnitudes and methods for assessing human and wildlife exposures to poly- and perfluoroalkyl substances (PFAS). Most human exposure assessments have focused on two to five legacy PFAS and wildlife assessments are typically limited to targeted PFAS (up to ~30 substances). However, shifts in chemical production are occurring rapidly and targeted methods for detecting PFAS have not kept pace with these changes. Total fluorine (TF) measurements complemented by suspect screening using high resolution mass spectrometry are thus emerging as essential tools for PFAS exposure assessment. Such methods enable researchers to better understand contributions from precursor compounds that degrade into terminal perfluoroalkyl acids (PFAA). Available data suggest that diet is the major human exposure pathway for some PFAS but there is large variability across populations and PFAS compounds. Additional data on TF in exposure media and the fraction of unidentified organofluorine are needed. Drinking water has been established as the major exposure source in contaminated communities. As water supplies are remediated, and for the general population, exposures from dust, personal care products, indoor environments and other sources may be more important. A major challenge for exposure assessments is the lack of statistically representative population surveys. For wildlife, bioaccumulation processes differ substantially between PFAS and neutral lipophilic organic compounds, prompting a revaluation of traditional bioaccumulation metrics. There is evidence that both phospholipids and proteins are important for the tissue partitioning and accumulation of PFAS. New mechanistic models for PFAS bioaccumulation are being developed that will assist in wildlife risk evaluations.
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| 3. |
- Eriksson, Ulrika, 1972-, et al.
(författare)
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Comparison of PFASs contamination in the freshwater and terrestrial environments by analysis of eggs from osprey (Pandion haliaetus), tawny owl (Strix aluco), and common kestrel (Falco tinnunculus)
- 2016
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Ingår i: Environmental Research. - San Diego, USA : Academic Press. - 0013-9351 .- 1096-0953. ; 149, s. 40-47
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Tidskriftsartikel (refereegranskat)abstract
- The level of PFAS (per- and polyfluorinated alkyl substances) contamination in freshwater and terrestrial Swedish environments in 2013/2014 was assessed by analyzing a range of perfluorinated alkyl acids, fluorotelomer acids, sulfonamides, sulfonamidoethanols and polyfluoralkyl phosphate diesters (diPAPs) in predator bird eggs. Stable isotopes ((13)C and (15)N) were analyzed to elucidate the dietary source. The tawny owl (Strix aluco, n=10) and common kestrel (Falco tinnunculus, n=40), two terrestrial species, and the osprey (Pandion haliaetus, n=30), a freshwater specie were included. In addition, a temporal trend (1997-2001, 2008-2009, 2013) in osprey was studied as well. The PFAS profile was dominated by perfluorooctane sulfonic acid (PFOS) in eggs from osprey and tawny owl, while for common kestrel perfluorinated carboxylic acids (∑PFCA) exceeded the level of PFOS. PFOS concentration in osprey eggs remained at the same level between 1997 and 2001 and 2013. For the long-chained PFCAs, there were a significant increase in concentrations in osprey eggs between 1997 and 2001 and 2008-2009. The levels of PFOS and PFCAs were about 10 and five times higher, respectively, in osprey compared to tawny owl and common kestrel. Evidence of direct exposure from PFCA precursor compounds to birds in both freshwater and terrestrial environment was observed. Low levels of diPAPs were detected in a few samples of osprey (<0.02-2.4ng/g) and common kestrel (<0.02-0.16ng/g) eggs, and 6:2 FTSA was detected in a majority of the osprey eggs (<6.3-52ng/g). One saturated telomer acid (7:3 FTCA), which is a transformation marker from precursor exposure, was detected in all species (<0.24-2.7ng/g). The (15)N data showed higher levels in osprey eggs compared to tawny owl and common kestrel, indicating that they feed on a 2-3 times higher trophic level. We conclude that ospreys are continuously exposed to PFAS at levels where adverse toxic effects have been observed in birds.
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| 4. |
- Eriksson, Ulrika, et al.
(författare)
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Perfluoroalkyl substances (PFASs) in food and water from Faroe Islands
- 2013
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Ingår i: Environmental Science and Pollution Research. - : Springer Science and Business Media LLC. - 0944-1344 .- 1614-7499. ; 20:11, s. 7940-7948
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Tidskriftsartikel (refereegranskat)abstract
- Diet and drinking water are suggested to be major exposure pathways for perfluoroalkyl substances (PFASs). In this study, food items and water from Faroe Islands sampled in 2011/2012 were analyzed for 11 perfluoroalkyl carboxylic acids (PFCAs) and 4 perfluoroalkane sulfonic acids (PFSAs). The food samples included milk, yoghurt, crSme fraiche, potatoes, fish, and fish feed, and the water samples included surface water and purified drinking water. In total, nine PFCAs and four PFSAs were detected. Generally, the levels of PFAS were in the lower picogram per gram range. Perfluorobutanoic acid was a major contributor to the total PFASs concentration in water samples and had a mean concentration of 750 pg/L. Perfluoroundecanoic acid (PFUnDA) was predominating in milk and wild fish with mean concentrations of 170 pg/g. Perfluorooctane sulfonic acid (PFOS) was most frequently detected in food items followed by PFUnDA, perfluorononanoic acid, and perfluorooctanoic acid (PFOA). Levels of PFUnDA and PFOA exceeded those of PFOS in milk and fish samples. Prevalence of long-chain PFCAs in Faroese food items and water is confirming earlier observations of their increase in Arctic biota. Predominance of short-chain and long-chain homologues indicates exposure from PFOS and PFOA replacement compounds.
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| 5. |
- Karlsson, Therese, 1987, et al.
(författare)
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Comparison between manta trawl and in situ pump filtration methods, and guidance for visual identification of microplastics in surface waters
- 2020
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Ingår i: Environmental Science and Pollution Research. - : Springer Science and Business Media LLC. - 0944-1344 .- 1614-7499. ; 27:5, s. 5559-5571
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Tidskriftsartikel (refereegranskat)abstract
- Owing to the development and adoption of a variety of methods for sampling and identifying microplastics, there is now data showing the presence of microplastics in surface waters from all over the world. The difference between the methods, however, hampers comparisons, and to date, most studies are qualitative rather than quantitative. In order to allow for a quantitative comparison of microplastics abundance, it is crucial to understand the differences between sampling methods. Therefore, a manta trawl and an in situ filtering pump were compared during realistic, but controlled, field tests. Identical microplastic analyses of all replicates allowed the differences between the methods with respect to (1) precision, (2) concentrations, and (3) composition to be assessed. The results show that the pump gave higher accuracy with respect to volume than the trawl. The trawl, however, sampled higher concentrations, which appeared to be due to a more efficient sampling of particles on the sea surface microlayer, such as expanded polystyrene and air-filled microspheres. The trawl also sampled a higher volume, which decreased statistical counting uncertainties. A key finding in this study was that, regardless of sampling method, it is critical that a sufficiently high volume is sampled to provide enough particles for statistical evaluation. Due to the patchiness of this type of contaminant, our data indicate that a minimum of 26 particles per sample should be recorded to allow for concentration comparisons and to avoid false null values. The necessary amount of replicates to detect temporal or spatial differences is also discussed. For compositional differences and size distributions, even higher particle counts would be necessary. Quantitative measurements and comparisons would also require an unbiased approach towards both visual and spectroscopic identification. To facilitate the development of such methods, a visual protocol that can be further developed to fit different needs is introduced and discussed. Some of the challenges encountered while using FTIR microspectroscopic particle identification are also critically discussed in relation to specific compositions found.
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| 6. |
- Karlsson, Therese, et al.
(författare)
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Provtagningsmetoder för mikroplast >300 μm i ytvatten : En jämförelsestudie mellan pump och trål
- 2018
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- Mikroplast (MP) är en föroreningstyp som medför stora utmaningar för provtagning och analys. För att kunna förbättra framtida miljöövervakning så jämfördes här två vanliga metoder för provtagning av mikroplast >300 μm; mantatrål och pump. Sex provreplikat för vardera metod togs under vindstilla förhållanden på ett och samma område under en dag. Provtagningsvolymen för varje replikat var 20 m3 för pumpen och ca 60 m3 för trålen. Efterföljande analys gjordes med visuell bedömning av en och samma person där antropogena partiklar delades in i elva kategorier.I pumpproverna hittades mellan 0 och 8 MPs som i volym räknat gav ett medelvärde av 0,17 MP/m3. I trålproverna varierade antalet mellan 9 och 33 MP som i volym räknat gav en signifikant högre koncentration än i trålproverna med ett medelvärde av 0,32 MP/m3. Resultaten innebar även att för att uppnå en statistisk power på 60 % så skulle tio pumpreplikat behövas för att mäta skillnaden mellan det undersökta området och ett område utan mikroplast. För trålen skulle motsvarande kräva 2 replikat. Alternativt kan en större provvolym ge en ökad säkerhet i och med att fördelningsdata då närmar sig en normalfördelning. Variationerna i mätosäkerhet mellan metoderna bedöms framförallt vara relaterad till skillnad i provvolym och skulle också kunna kompenseras genom ökad pumpvolym, vilket skulle gå något snabbare jämfört med att göra fler replikat.Sammansättningen av MP varierade en del mellan replikaten men bestod främst av expanderad cellplast, filmer, filament, och fragment. I vartdera pumpprov var det i genomsnitt 1,3 filmer och 0,33 expanderade cellplastpartiklar medan trålen hade i genomsnitt 2,5 filmer och 9,2 expanderade cellplastpartiklar. Per volymenhet utgjorde filmer den största delen av MP i prover tagna med pump (40 %), medan cellplast dominerade i trålproverna (46 %). Cellplast tycks därmed provtas mer effektivt med trål vilket kan bero på att den flyter på det översta ytlagret som trålen provtar. Pumpen ligger något lägre i ytskiktet och jämförelsestudien indikerar att de båda provtagarna har en mer jämförbar provsammansättning för partiklar med en mer neutral flytkraft. I denna studie erhölls dock inte tillräckligt stort antal partiklar av olika plasttyper för att tillåta mer ingående statistiska jämförelser mellan provsammansättningarna.Sannolikheten för att få falska nollvärden ökar vid lägre partikelantal vilket börjar få en signifikant effekt under 5 partiklar per prov. Oavsett vilken metod som används är det viktigt att tillräckligt stor volym provtas för att besvara frågeställningar som skillnader mellan olika områden och skillnader mellan olika sorters plast.Bakgrund och syfte med rapportenÄven om metoder för provtagning, extraktion och identifikation av mikroplast har utvecklats snabbt under senare år så återstår ännu flera utmaningar. Flertalet studier publicerar förekomst av mikroplast i sjöar och hav. En av de utmaningarna består i hur vi på ett representativt sätt ska kunna provta en förorening som är så pass heterogen, både till form och också utbredning. En annan frågeställning är huruvida det går att jämföra resultat från två olika provtagningsmetoder. Här jämför vi två metoder som ofta används för att provta mikroplast med storlek över 300 μm i ytvatten; en mantatrål och en pump. Under en dag (10 oktober 2017) togs 6 replikat per metod på samma plats i Gullmarsfjorden utanför Lysekil. Genom att räkna mikroplast och annat mikroskräp i proverna var syftet att undersöka skillnader mellan replikat och skillnader mellan metoderna.Jämförelsen har gjorts på uppdrag av Naturvårdsverket och Havs- och vattenmyndigheten som ett led i arbetet med att utveckla övervakning av mikroskräp.
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| 7. |
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| 8. |
- Mattsson, Anna, et al.
(författare)
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Developmental exposure to a mixture of perfluoroalkyl acids (PFAAs) affects the thyroid hormone system and the bursa of Fabricius in the chicken
- 2019
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Ingår i: Scientific Reports. - : Nature Publishing Group. - 2045-2322. ; 9:1
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Tidskriftsartikel (refereegranskat)abstract
- Perfluoroalkyl acids (PFAAs) are ubiquitous environmental contaminants and eggs and nestlings of raptors and fish-eating birds often contain high levels of PFAAs. We studied developmental effects of a mixture of ten PFAAs by exposing chicken embryos to 0.5 or 3 μg/g egg of each compound in the mixture. Histological changes of the thyroid gland were noted at both doses and increased expression of mRNA coding for type III deiodinase was found at 0.5 μg/g egg. Serum concentrations of the free fraction of thyroid hormones (T3 and T4) were reduced by the PFAA mixture at 3 µg/g egg, which is in line with a decreased synthesis and increased turnover of thyroid hormones as indicated by our histological findings and the decreased mRNA expression of type III deiodinase. The relative weight of the bursa of Fabricius increased at a dose of 3 μg/g egg in females. The bursa is the site of B-cell development in birds and is crucial for the avian adaptive immune system. Analysis of plasma and liver concentrations of the mixture components showed differences depending on chain length and functional group. Our results highlight the vulnerability of the thyroid hormone and immune systems to PFAAs.
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| 9. |
- Mattsson, Anna, et al.
(författare)
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Metabolic Profiling of Chicken Embryos Exposed to Perfluorooctanoic Acid ( PFOA) and Agonists to Peroxisome Proliferator-Activated Receptors
- 2015
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Ingår i: PLOS ONE. - : Public Library Science. - 1932-6203. ; 10:12
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Tidskriftsartikel (refereegranskat)abstract
- Untargeted metabolic profiling of body fluids in experimental animals and humans exposed to chemicals may reveal early signs of toxicity and indicate toxicity pathways. Avian embryos develop separately from their mothers, which gives unique possibilities to study effects of chemicals during embryo development with minimal confounding factors from the mother. In this study we explored blood plasma and allantoic fluid from chicken embryos as matrices for revealing metabolic changes caused by exposure to chemicals during embryonic development. Embryos were exposed via egg injection on day 7 to the environmental pollutant perfluorooctanoic acid (PFOA), and effects on the metabolic profile on day 12 were compared with those caused by GW7647 and rosiglitazone, which are selective agonists to peroxisome-proliferator activated receptor a (PPAR alpha) and PPAR gamma, respectively. Analysis of the metabolite concentrations from allantoic fluid by Orthogonal Partial Least Squares Discriminant Analysis (OPLS-DA) showed clear separation between the embryos exposed to GW7647, rosiglitazone, and vehicle control, respectively. In blood plasma only GW7647 caused a significant effect on the metabolic profile. PFOA induced embryo mortality and increased relative liver weight at the highest dose. Sublethal doses of PFOA did not significantly affect the metabolic profile in either matrix, although single metabolites appeared to be altered. Neonatal mortality by PFOA in the mouse has been suggested to be mediated via activation of PPAR alpha. However, we found no similarity in the metabolite profile of chicken embryos exposed to PFOA with those of embryos exposed to PPAR agonists. This indicates that PFOA does not activate PPAR pathways in our model at concentrations in eggs and embryos well above those found in wild birds. The present study suggests that allantoic fluid and plasma from chicken embryos are useful and complementary matrices for exploring effects on the metabolic profile resulting from chemical exposure during embryonic development.
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| 10. |
- Nilsson, Helena, 1974-, et al.
(författare)
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A time trend study of significantly elevated perfluorocarboxylate levels in humans after using fluorinated ski wax
- 2010
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Ingår i: Environmental Science and Technology. - Washington, USA : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 44:6, s. 2150-2155
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Tidskriftsartikel (refereegranskat)abstract
- A time trend study focusing on ski waxing technicians' exposure to perfluorinated chemicals (PFCs) from fluorinated wax fumes was performed in 2007/2008. Levels of eight perfluorocarboxylates and three perfluorosulfonates were analyzed in monthly blood samples from eight technicians, Samples were collected before the ski season, i.e., preseason, then at four AS World Cup competitions in cross country skiing, and finally during an unexposed 5-month postseason period. The perfluorinated carboxylates perfluoroheptanoic acid (PFHpA), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUnDA) bioaccumulate, and continued exposure may contribute to elevated levels in ski technicians compared to the general population. The wax technicians' median blood level of PFOA is 112 ng/mL compared to 2.5 ng/mL in the general Swedish population. A significant correlation was found between number of working years and levels of perfluorocarboxylates. The PFOA levels in three technicians with "low" initial levels of PFOA (< 10.0 ng/mL in preseason blood) increased by 254, 134, and 120%, whereas five technicians with "high" initial levels (> 100 ng/mL in preseason sample) were at steady state. PFHxA is suggested to have a short half-life in humans relative the other perfluorocarboxylates. The levels of perfluorosulfonates were unaffected by the wax exposure.
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| 11. |
- Nilsson, Helena, 1974-, et al.
(författare)
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Biotransformation of fluorotelomer compound to perfluorocarboxylates in humans
- 2013
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Ingår i: Environment International. - : Elsevier. - 0160-4120 .- 1873-6750. ; 51, s. 8-12
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Tidskriftsartikel (refereegranskat)abstract
- Levels of perfluorocarboxylates (PFCAs) in biological compartments have been known for some time but their transport routes and distribution patterns are not properly elucidated. The opinions diverge whether the exposure of the general population occurs indirect through precursors or direct via PFCAs. Previous results showed that ski wax technicians are exposed to levels up to 92 000 ng/m(3) of 8:2 fluorotelomer alcohol (FTOH) via air and have elevated blood levels of PFCAs. Blood samples were collected in 2007-2011 and analyzed for C(4)-C(18) PFCAs, 6:2, 8:2 and 10:2 unsaturated fluorotelomer acids (FTUCAs) and 3:3, 5:3 and 7:3 fluorotelomer acids (FTCAs) using UPLC-MS/MS. Perfluorooctanoic acid (PFOA) was detected in levels ranging from 1.90 to 628 ng/mL whole blood (wb). Metabolic intermediates 5:3 and 7:3 FTCA were detected in all samples at levels up to 6.1 and 3.9 ng/mL wb. 6:2, 8:2 and 10:2 FTUCAs showed maximum levels of 0.07, 0.64 and 0.11 ng/mL wb. Also, for the first time levels of PFHxDA and PFOcDA were detected in the human blood at mean concentrations up to 4.22 ng/mL wb and 4.25 ng/mL wb respectively. The aim of this study was to determine concentrations of PFCAs and FTOH metabolites in blood from ski wax technicians.
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| 12. |
- Nilsson, Helena, 1974-, et al.
(författare)
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Inhalation exposure to fluorotelomer alcohols yield perfluorocarboxylates in human blood?
- 2010
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Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 44:19, s. 7717-7722
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Tidskriftsartikel (refereegranskat)abstract
- Levels of perfluorinated carboxylates (PFCAs) in different environmental and biological compartments have been known for some time, but the routes of exposure still remain unclear. The opinions are divergent whether the exposure to general populations occurs mainly indirect through precursor compounds or direct via PFCAs. Previous results showed elevated blood levels of PFCAs in ski wax technicians compared to a general population. The objective of this follow-up study was to determine concentrations of PFCAs, perfluorosulfonates (PFSAs), and fluorotelomer alcohols (FTOHs), precursor compounds that are known to degrade to PFCAs, in air collected in the breathing zone of ski wax technicians during work. We collected air samples by using ISOLUTE ENV+ cartridges connected to portable air pumps with an air flow of 2.0 L min(-1). PFCAs C5-C11 and PFSAs C4, C6, C8, and C10 were analyzed using LC-MS/MS and FTOHs 6:2, 8:2, and 10:2 with GC-MS/MS. The results show daily inhalation exposure of 8:2 FTOH in mu g/m(3) air which is up to 800 times higher than levels of PFOA with individual levels ranging between 830-255000 ng/m(3) air. This suggests internal exposure of PFOA through biotransformation of 8:2 FTOH to PFOA and PFNA in humans.
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| 13. |
- Nilsson, Helena, 1974-, et al.
(författare)
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Professional ski waxers' exposure to PFAS and aerosol concentrations in gas phase and different particle size fractions
- 2013
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Ingår i: Environmental science. Processes & impacts. - : Royal Society of Chemistry. - 2050-7887 .- 2050-7895. ; 15:4, s. 814-822
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Tidskriftsartikel (refereegranskat)abstract
- Previous reports show that professional ski waxers have elevated blood levels of perfluorinated substances (PFAS) such as perfluorooctanoate (PFOA) and are exposed to very high concentrations of PFAS in air during ski waxing. Aerosol exposure increases the risk of cardiovascular disease, and PFOA is a potential hormonal disruptor and carcinogen, and can affect the fatty acid metabolism. Animal studies have shown that 8: 2 FTOH can undergo biotransformation to PFOA. For the first time, this study presents an occupational scenario of professional ski waxers who are exposed to extremely high dust levels as well as per-and polyfluorinated compounds. Personal and fixed measurements of total aerosol, inhalable and respirable fractions were performed during World Cup events 2007-2010. The occupational exposure limit (OEL) is exceeded in 37% of the personal measurements with concentrations up to 15 mu g m(-3) in air. There are differences between personal and area total aerosol concentrations with levels from personal measurements twice as high as those from the area measurements. The personal levels for FTOH ranged up to 996 mg m(-3) (mean = 114 mu g m(-3)) and for PFOA up to 4.89 mu g m(-3) (mean = 0.53 mu g m(-3)) in ENV+ sorbent samples as compared to the general exposure levels from air reaching only low ng m(-3) (<30 ng m(-3)) levels. FTOHs were not detected in aerosols but PFOA showed an average level of 12 mu g m(-3) (range = 1.2-47 mu g m(-3)). The ski waxers' exposure to paraffin fumes and PFAS is not in compliance with the occupational exposure standards and by far exceed the general populations' exposure. Preventive measures must be taken to minimize the exposure in this occupational group.
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| 14. |
- Persson, Sara, et al.
(författare)
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Perfluoroalkyl acids in subarctic wild male mink (Neovison vison) in relation to age, season and geographical area
- 2013
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Ingår i: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 59, s. 425-430
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Tidskriftsartikel (refereegranskat)abstract
- This study investigates the influence of biological and environmental factors on the concentrations of perfluoroalkyl acids (PFAAs) in a top predator; the American mink Perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), perfluorooctane sulfonate (PFOS) and perfluoroalkyl carboxylates (PFCAs) with C-8-C-13 perfluorinated carbon chains were analyzed in livers from wild male mink liver (n = 101) from four areas in Sweden representing two inland environments (rural and highly anthropogenic, respectively) and two different coastal environments. Mean PFOS concentrations were 1250 ng/g wet weight and some mink from the urban inland area had among the highest PFOS concentrations ever recorded in mink (up to 21 800 ng/g wet weight). PFBS was detected in 89% of the samples, but in low concentrations (mean 0.6 ng/g ww). There were significant differences in PFAA concentrations between the geographical areas (p < 0.001-0.01). Age, body condition and body weight did not influence the concentrations significantly, but there was a seasonal influence on the concentrations of perfluorodecanoic acid (PFDA) and perfluoroundecanoic acid (PFUnDA) (p < 0.01 and p < 0.05, respectively), with lower concentrations in autumn samples than in samples taken" in the winter and spring. It is thus recommended to take possible seasonal differences into account when using mink exposure data. The overall results suggest that the mink is a suitable sentinel species for assessing and monitoring environmental levels of PFAAs. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
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| 15. |
- Roos, Anna Maria, et al.
(författare)
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Perfluoroalkyl substances in circum-ArcticRangifer : caribou and reindeer
- 2022
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Ingår i: Environmental Science and Pollution Research. - : Springer. - 0944-1344 .- 1614-7499. ; 29:16, s. 23721-23735
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Tidskriftsartikel (refereegranskat)abstract
- Livers of caribou and reindeer (Rangifer tarandus) from Canada (n = 146), Greenland (n = 30), Svalbard (n = 7), and Sweden (n = 60) were analyzed for concentrations of eight perfluoroalkyl carboxylic acids and four perfluoroalkane sulfonic acids. In Canadian caribou, PFNA (range < 0.01-7.4 ng/g wet weight, ww) and PFUnDA (<0.01-5.6 ng/g ww) dominated, whereas PFOS predominated in samples from South Greenland, Svalbard, and Sweden, although the highest concentrations were found in caribou from Southwest Greenland (up to 28 ng/g ww). We found the highest median concentrations of all PFAS except PFHxS in Akia-Maniitsoq caribou (Southwest Greenland, PFOS 7.2-19 ng/g ww, median 15 ng/g ww). The highest concentrations of ΣPFAS were also found in Akia-Maniitoq caribou (101 ng/g ww) followed by the nearby Kangerlussuaq caribou (45 ng/g ww), where the largest airport in Greenland is situated, along with a former military base. Decreasing trends in concentrations were seen for PFOS in the one Canadian and three Swedish populations. Furthermore, PFNA, PFDA, PFUnDA, PFDoDA, and PFTrDA showed decreasing trends in Canada's Porcupine caribou between 2005 and 2016. In Sweden, PFHxS increased in the reindeer from Norrbotten between 2003 and 2011. The reindeer from Västerbotten had higher concentrations of PFNA and lower concentrations of PFHxS in 2010 compared to 2002. Finally, we observed higher concentrations in 2010 compared to 2002 (albeit statistically insignificant) for PFHxS in Jämtland, while PFNA, PFDA, PFUnDA, PFDoDA, and PFTrDA showed no difference at all.
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| 16. |
- Rotander, Anna, 1978-, et al.
(författare)
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Increasing levels of long-chain perfluorocarboxylic acids (PFCAs) in Arctic and North Atlantic marine mammals, 1984-2009
- 2012
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Ingår i: Chemosphere. - : Elsevier. - 0045-6535 .- 1879-1298. ; 86:3, s. 278-285
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Tidskriftsartikel (refereegranskat)abstract
- Temporal variations in concentrations of perfluorinated carboxylic acids (PFCAs) and sulfonic acids (PFSAs), including perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) structural isomers, were examined in livers of pilot whale (Globicephala melas), ringed seal (Phoca hisida), minke whale (Balaenoptera acutorostrata), harbor porpoise (Phocoena phocoena), hooded seal (Cystophora cristata), Atlantic white-sided dolphin (Lagenorhynchus acutus) and in muscle tissue of fin whales (Balaenoptera physalus). The sampling spanned over 20 years (1984-2009) and covered a large geographical area of the North Atlantic and West Greenland. Liver and muscle samples were homogenized, extracted with acetonitrile, cleaned up using hexane and solid phase extraction (SPE), and analyzed by liquid chromatography with negative electrospray tandem mass spectrometry (LC-MS/MS). In general, the levels of the long-chained PFCAs (C9-C12) increased whereas the levels of PFOS remained steady over the studied period. The PFOS isomer pattern in pilot whale liver was relatively constant over the sampling years. However, in ringed seals there seemed to be a decrease in linear PFOS (L-PFOS) with time, going from 91% in 1984 to 83% in 2006.
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| 17. |
- Rotander, Anna, 1978-, et al.
(författare)
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Microplastics in Södertälje : From Lake Mälaren to the Baltic Sea
- 2019
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Rapport (övrigt vetenskapligt/konstnärligt)abstract
- 3Svensk sammanfattningTrots att ett ökat antal studier de senaste åren slagit fast att betydande mängder mikroplaster kontinuerligt släpps ut i den marina miljön så finns det en utbredd okunskap vad gäller vilka källor som bidrar mest. Det finns således ett behov av att identifiera och karakterisera punktkällor för utsläpp av mikroplaster.Den här studien har genomförts i Södertälje och prover har tagits uppströms Södertälje i Mälaren och nedströms till Östersjön. Området är förutom befolkningen påverkat av olika typer av industrier. Södertäljeviken är väldefinierad och har få tillflöden förutom från avrinning från staden och industriområden. Syftet med studien är att studera källor och spridning av mikroplaster till havet genom att analysera hur Södertäljeområdet påverkar förekomst och typ av mikroplaster i ytvatten och sediment.Ytvatten provtogs i nio stycken lokaler i Södertäljeviken, inklusive två tillflöden, vid två tillfällen under hösten 2017. Vid sex av dessa lokaler och vid ett tillfälle togs även sedimentkärnor. Ytvatten provtags med en pump som sorterade in partiklarna i två fraktioner: >300 μm och 50-300 μm. Halterna mikroskräppartiklar (mikroplast, fibrer och övriga antropogena partiklar) var i samtliga ytvattenprover högre i 50-300 μm fraktionen med skillnader som varierade mellan ca en faktor 5 och faktor 160. Halterna mikroplaster >300 μm i ytvatten varierade mellan 0.1 och 1 partiklar/m3. Det relativt låga antalet mikroplaster i kombination med variationer mellan de två tidpunkterna i halter försvårar slutsatserna om punktkällor.De vanligaste polymererna visade sig vara polyeten och polypropen baserat på analys med infraröd spektroskopi. Hälften av partiklarna som testades kunde dock inte tillskrivas en polymertyp och hamnade i kategorin "oidentifierad polymer". Ett karakteristiskt format rött fragment återfanns i flera av ytvattenproverna och sedimentproverna och var sannolikt färgflagor efter t.ex. bottenfärg.Halterna i ytvatten är jämförbara med studier från Östersjön, Gullmarsfjorden och Nyköpingsåarna (Nyköpingsån, Kilaån, Svärtaån och Trosaån) men lägre jämfört med ytvatten i Göteborg (Mölndalsån, Kvillebäcken, Säveån, Lärjeån och Stora ån).Halten mikroplast i ytvatten ökade inte nämnvärt från bakgrundsnivån i referenspunkten i Mälaren till början av Södertäljeviken (Snäckviken) med industrier, båttrafik osv. samt till centrala Södertälje (Maren) där Mälaren möter Östersjön. Nedströms centrum kunde en viss ökning av ytvattenhalten urskiljas i lokalen Igelstaviken med sina större industrier och Södertälje hamn. Halten mikroplast minskade sedan nedströms och ut i Östersjön. Detta överensstämde med sedimentproverna, dock kan man i ytsedimentet se en ökning redan i Snäckviken.Resultaten tyder på att det finns punktkällor kopplade till lokalerna Igelstaviken och Torpaviken men deras betydelse för det totala utsläppet av MP från land är inte fastlagd. Både båttrafik, industrier, och värmeverk finns kopplade till lokalerna. Inga kända plasttillverkare finns i områdena och det bör därför utredas hur mycket mikroplast som släpps ut från övrig tillverkningsindustri. Sedimentresultaten visar på gradienter med ökande halt i Södertäljeviken fram till Igelsta och därefter en gradvis minskande halt nedströms. Halten mikroplast i sediment är högre i bakgrundslokalen i Östersjön jämfört med bakgrundslokalen i Mälaren vilket tyder på en påverkan från Södertälje. Fler sedimentprov behöver analyseras för att säkerställa skillnaden då variationen av mikroplast i sediment inte är känd.
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| 18. |
- Rotander, Anna, et al.
(författare)
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Novel fluorinated surfactants tentatively identified in firefighters using liquid chromatography quadrupole time-of-flight tandem mass spectrometry and a case-control approach
- 2015
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Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 49:4, s. 2434-2442
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Tidskriftsartikel (refereegranskat)abstract
- Fluorinated surfactant-based aqueous film-forming foams (AFFFs) are made up of per- and polyfluorinated alkyl substances (PFAS) and are used to extinguish fires involving highly flammable liquids. The use of perfluorooctanesulfonic acid (PFOS) and other perfluoroalkyl acids (PFAAs) in some AFFF formulations has been linked to substantial environmental contamination. Recent studies have identified a large number of novel and infrequently reported fluorinated surfactants in different AFFF formulations. In this study, a strategy based on a case-control approach using quadrupole time-of-flight tandem mass spectrometry (QTOF-MS/MS) and advanced statistical methods has been used to extract and identify known and unknown PFAS in human serum associated with AFFF-exposed firefighters. Two target sulfonic acids [PFOS and perfluorohexanesulfonic acid (PFHxS)], three non-target acids [perfluoropentanesulfonic acid (PFPeS), perfluoroheptanesulfonic acid (PFHpS), and perfluorononanesulfonic acid (PFNS)], and four unknown sulfonic acids (Cl-PFOS, ketone-PFOS, ether-PFHxS, and Cl-PFHxS) were exclusively or significantly more frequently detected at higher levels in firefighters compared to controls. The application of this strategy has allowed for identification of previously unreported fluorinated chemicals in a timely and cost-efficient way.
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| 19. |
- Schönlau, Christine, 1986-, et al.
(författare)
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Aryl hydrocarbon receptor-mediated potencies in field-deployed plastics vary by type of polymer
- 2019
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Ingår i: Environmental Science and Pollution Research. - : Springer. - 0944-1344 .- 1614-7499. ; 26:9, s. 9097-9088
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Tidskriftsartikel (refereegranskat)abstract
- Plastic is able to sorb environmental pollutants from ambient water and might act as a vector for these pollutants to marine organisms. The potential toxicological effects of plastic-sorbed pollutants in marine organisms have not been thoroughly assessed. In this study, organic extracts from four types of plastic deployed for 9 or 12 months in San Diego Bay, California, were examined for their potential to activate the aryl hydrocarbon receptor (AhR) pathway by use of the H4IIE-luc assay. Polycyclic aromatic hydrocarbons (PAH), including the 16 priority PAHs, were quantified. The AhR-mediated potency in the deployed plastic samples, calculated as bio-TEQ values, ranged from 2.7 pg/g in polyethylene terephthalate (PET) to 277 pg/g in low-density polyethylene (LDPE). Concentrations of the sum of 24 PAHs in the deployed samples ranged from 4.6 to 1068 ng/g. By use of relative potency factors (REP), a potency balance between the biological effect (bio-TEQs) and the targeted PAHs (chem-TEQs) was calculated to 24-170%. The study reports, for the first time, in vitro AhR-mediated potencies for different deployed plastics, of which LDPE elicited the greatest concentration of bio-TEQs followed by polypropylene (PP), PET, and polyvinylchloride (PVC).
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| 20. |
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| 21. |
- Schönlau, C., et al.
(författare)
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Microplastics in sea-surface waters surrounding Sweden sampled by manta trawl and in-situ pump
- 2020
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Ingår i: Marine Pollution Bulletin. - : Elsevier. - 0025-326X .- 1879-3363. ; 153
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Tidskriftsartikel (refereegranskat)abstract
- Microplastics were sampled in open surface waters by using a manta trawl and an in-situ filtering pump. A total of 24 trawl samples and 11 pump samples were taken at 12 locations around Sweden. Overall, the concentration of microplastic particles was higher in pump samples compared to trawl samples. The median microplastic particle concentration was 0.04 particles per m−3 for manta trawl samples and 0.10 particles per m−3 in pump samples taken with a mesh size of 0.3 mm. The highest concentrations were recorded on the west coast of Sweden. Fibers were found in all samples and were also more frequent in the pump samples. Even higher concentrations of fibers and particles were found on the 0.05 mm pump filters. Using near-infrared hyperspectral imaging the majority of the particles were identified as polyethylene followed by polypropylene.
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| 22. |
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| 23. |
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| 24. |
- Aro, Rudolf, 1992-, et al.
(författare)
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Combustion ion chromatography for extractable organofluorine analysis
- 2021
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Ingår i: iScience. - : Cell Press. - 2589-0042. ; 24:9
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Tidskriftsartikel (refereegranskat)abstract
- Combustion ion chromatography (CIC) has found a role in environmental analytical chemistry for fluorine content analysis. It is used for extractable organofluorine (EOF) analysis to evaluate perfluoroalkyl and polyfluoroalkyl substances (PFASs) and other organofluorine burden. The prevailing assumption has been that all PFASs are incinerated in CIC and matrix components have no impact on this process, but this has not been experimentally evaluated. In this work, the combustion efficiencies of 13 different PFASs were determined (66-110%). A notable difference was observed between calibrating the CIC with inorganic fluorine or organofluorine. Potential interferences from cations and coextracted matrix components from whole blood and surface water samples were evaluated. These observations should be acknowledged when performing EOF analysis using CIC, overlooking either non-100% combustion efficiencies or the differences in calibrating the CIC with inorganic fluorine or organofluorine could lead to underestimating EOF content and through that to misguide policy decisions.
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| 25. |
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