Biomedical subjects

Kristoffer Naes

Publications and source records attributed to Kristoffer Naes.

9 recordsLinked to original sources

PubMed2006

Modelling the long-term fate of polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs) in the Grenland Fjords, Norway.

The development and application of a predictive fate model (DIG--Dioxins in Grenland) for polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F) in the marine environment of the Norwegian Grenland Fjords are described. The objective of the modelling study was to predict long-term future changes in PCDD/F concentrations in the fjord following the cessation of point source emissions. To assess the reliability of the model, the model performance was evaluated by comparing model results to field measurements collected between 1989 and 2001. Model bias (defined as the ratio of median predicted concentration and median observed concentration) for prediction of concentrations for three different PCDD/F congeners (2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), 1,2,3,6,7,8-hexadibenzofuran (HxCDF) and octachlorodibenzofuran (OCDF)) in the fjord was between 0.53 and 24, which was deemed a satisfactory result for models of this type. The model was run to determine the dynamic change in concentrations between 1950 and 2050 and to examine the key fluxes of PCDD/Fs in the fjord. Between 1990 and 2050 sediment concentrations of TCDD, HxCDF and OCDF were predicted to fall at fairly constant but gradually slowing rates to concentrations 52, 98 and 88 times lower, respectively, of their 1990 values. Losses of PCDD/Fs from the bottom sediments in the Frierfjord were predicted to be a combination of sediment burial and net resuspension to the water column. Sediment burial was shown to be relatively more important in the fjord's deep-water sediments, whereas resuspension was relatively more important in the shallow sediments. For the shallower sediments, a net water-to-sediment flux was predicted for all three congeners up until the mid-1970s, when emission reductions were initiated, and thereafter a net sediment-to-water flux was predicted. The shallow sediments acted as net sources to the deeper sediments and to the fishing areas in the outer fjord.

Benzofurans↗

PubMed2006

Polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) in the Grenlandfjords (Norway)--disposition, levels, and effects.

Polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) are regarded as highly toxic. Their lipophilicity and persistence also render them subject to bioaccumulation. The Grenlandfjords (southern Norway) have long been polluted by PCDD/Fs through the magnesium production at Herøya (1951-2002). Therefore, extensive environmental monitoring was performed in the area, and the project "Dioxins in the Grenlandfjords--DIG" was launched to study abiotic mass balances, biotic processes and ecological risk. This article describes some results from DIG on the dispositions of PCDD/Fs in the food web and biological effects. Furthermore, data from the Norwegian monitoring of the Grenlandfjords are described. Differences in cod liver PCDD/F levels were found between stations, with the highest concentrations in the inner fjord (the Frierfjord), closest to the pollution source. Furthermore, considerable decreases in the concentrations followed the large discharge reductions (1975 and 1990). Contrary to earlier food web studies on other organochlorines, it was found that the concentrations of PCDD/Fs decline with higher trophic level. Higher chlorinated congeners also constituted a lower percentage of sigmaPCDD/Fs higher in the food chain. The results indicated a limited bioaccumulation of PCDD/Fs, especially of higher chlorinated congeners, likely due to reduced membrane permeability (high molecular size), and possibly slow transport through intestinal aqueous phases. Hepatic cod 7-ethoxyresorufin O-deethylase (EROD) activities differed between the Frierfjord and the Eidangerfjord, showing the different PCDD/F exposure in the two fjords. Furthermore, seasonal variations in cytochrome P-450 (CYP) 1A activity were shown, with different responses between genders. The differences were likely linked to the reproductive cycle of the fish.

Animals↗

PubMed2006

Flows of dioxins and furans in coastal food webs: inverse modeling, sensitivity analysis, and applications of linear system theory.

Rate constant bioaccumulation models are applied to simulate the flow of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in the coastal marine food web of Frierfjorden, a contaminated fjord in southern Norway. We apply two different ways to parameterize the rate constants in the model, global sensitivity analysis of the models using Extended Fourier Amplitude Sensitivity Test (Extended FAST) method, as well as results from general linear system theory, in order to obtain a more thorough insight to the system's behavior and to the flow pathways of the PCDD/Fs. We calibrate our models against observed body concentrations of PCDD/Fs in the food web of Frierfjorden. Differences between the predictions from the two models (using the same forcing and parameter values) are of the same magnitude as their individual deviations from observations, and the models can be said to perform about equally well in our case. Sensitivity analysis indicates that the success or failure of the models in predicting the PCDD/F concentrations in the food web organisms highly depends on the adequate estimation of the truly dissolved concentrations in water and sediment pore water. We discuss the pros and cons of such models in understanding and estimating the present and future concentrations and bioaccumulation of persistent organic pollutants in aquatic food webs.

Animals↗

PubMed2006

Bioaccumulation of native polycyclic aromatic hydrocarbons from sediment by a polychaete and a gastropod: freely dissolved concentrations and activated carbon amendment.

The present paper describes a study on the bioaccumulation of native polycyclic aromatic hydrocarbons (PAHs) from three harbors in Norway using the polychaete Nereis diversicolor and the gastropod Hinia reticulata. First, biota-sediment accumulation factors (BSAFs) were measured in laboratory bioassays using the original sediments. Median BSAFs were 0.004 to 0.01 kg organic carbon/kg lipid (10 PAHs and 6 organism-sediment combinations), which was a factor of 89 to 240 below the theoretical BSAF based on total sediment contents (which is approximately one). However, if BSAFs were calculated on the basis of measured freely dissolved PAH concentrations in the pore water (measured with polyoxymethylene passive samplers), it appeared that these BSAFfree values agreed well with the measured BSAFs, within a factor of 1.7 to 4.3 (median values for 10 PAHs and six organism-sediment combinations). This means that for bioaccumulation, freely dissolved pore-water concentrations appear to be a much better measure than total sediment contents. Second, we tested the effect of 2% (of sediment dry wt) activated carbon (AC) amendments on BSAE The BSAFs were significantly reduced by a factor of six to seven for N. diversicolor in two sediments (i.e., two of six organism-sediment combinations), whereas no significant reduction was observed for H. reticulata. This implies that either site-specific evaluations of AC amendment are necessary, using several site-relevant benthic organisms, or that the physiology of H. reticulata caused artifactually high BSAF values in the presence of AC.

Animals↗

PubMed2005

Distribution of PCNs, PCBs, and other POPs together with soot and other organic matter in the marine environment of the Grenlandsfjords, Norway.

The apparently dissolved concentration of polychlorinated naphthalenes (PCNs) and three planar polychlorinated biphenyls (pPCBs) were sampled and analysed in the water column of a marine fjord system. We also measured how much of these persistent organic pollutants (POPs) were associated with suspended particles. The field observations showed that an unexpectedly high portion of the pollutants were particle-associated. The factor of deviation from model predictions had positive linear regression on the soot carbon:particulate organic carbon ratio of the particles, and on estimates of the soot-water distribution coefficient for the PCNs. The spatial distribution of surface sediment concentrations of PCNs and polycyclic aromatic hydrocarbons (PAH) were found to consistently follow the sediment content of soot (f(SC)) to a larger extent than the bulk organic matter (f(OC)). There were no systematic differences in the strength of correlation of sediments concentrations of other POPs, i.e. octachlorostyrene and organochlorine pesticides with sediment concentration to f(SC) and f(OC). Mechanisms possible of generating these types of observations, e.g. adsorption to soot carbon in the marine particle, are discussed.

Animals↗

PubMed2005

Testing common sediment-porewater distribution models for their ability to predict dissolved concentrations of POPs in The Grenlandsfjords, Norway.

This study compares in situ observed porewater concentration of persistent organic pollutants (POPs) with predictions by common solid-water phase distribution models. Bottom sediments were sampled in The Grenlandsfjords, Norway, and the interstitial porewater was isolated from the solids by centrifugation and filtration. Both phases were analysed for polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/F), polycyclic aromatic hydrocarbons (PAH), and organic carbon. Based on the sediments' solid phase content of POPs, organic carbon, and soot carbon, we used the organic matter partitioning (OMP), and also the soot and organic matter partitioning (SOMP) model to estimate the porewater concentration. The OMP model gave better agreement to observations than the SOMP model for both PCDD/Fs and PAHs. The observed concentration of the PCDD/Fs in the sediments' porewater was much higher than in the deep water of the fjord. The logarithm of the organic matter-water partitioning coefficent (log K(OC)) in the porewater had positive linear regression on the logarithm of the octanol-water partitioning coefficient (log K(OW)). The slope of the regression model was indistinguishable from 1, except for the PAHs as a group which had a slope less than 1. This contrasts to previous studies undertaken in The Grenlandsfjords water column, where the slopes were higher than 1 for PCDD/Fs, and the K(OC) were much higher than the K(OW). One explanation may be that the influence of POPs adsorption to soots decrease because competitive sorption by other compounds in the sediment are higher than in the water column. This indicates that the sorption isotherms for these POPs need better understanding in order to be applicable in both the water column and the porewater.

Algorithms↗

PubMed2003

Polycyclic aromatic hydrocarbons (PAHs) and organochlorines (OCs) in bottom sediments of the Guba Pechenga, Barents Sea, Russia.

Surface sediment samples from the Guba Penchenga and adjacent areas: Varangerfjord, Guba Malaya Volokovaya and Guba Bol'shaya Volokovaya (south-western Barents Sea) collected in March-April 1997 were analysed for polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), chlorinated pesticides: p,p'-DDT, p,p'-DDE, p,p'-DDD, alpha- and gamma-HCH, and hexachlorobenzene (HCB). Mean summation operator PAH (sum of the two- to six-ring PAHs) concentration in sediments from the Guba Pechenga (1481 ng/g dry wt.) was significantly higher than in sediments from adjacent areas (252 ng/g dry wt.), where PAH contamination levels were similar to reported for unpolluted sediments of the northern Norway fjords and open parts of the Barents Sea. Differences between HCB levels as well as summation operator HCH (sum of alpha- and gamma-HCH) levels found in Guba Pechenga sediments and adjacent area sediments were not significant. Concentrations of these contaminants varied in ranges 0.28-1.76 and 0.05-0.68 ng/g dry wt., respectively, and were consistent with literature data on PAH levels in sediments from the northern Norway harbours, Kola Bay (Russia) and south-eastern part of the Barents Sea. Average total DDT concentration in Guba Pechenga sediments (10.5 ng/g dry wt.) was one and 2-3 orders higher than those found in sediments from the Pechora Sea and from the seas of eastern Arctic, respectively, however, it was comparable with DDT levels reported for harbours of northern Norway and Kola Bay. Significant difference between total DDT levels in Guba Pechenga and in the adjacent areas (mean 1.8 ng/g) was found. Among compounds of DDT family, p,p'-DDT isomer prevailed in all sediment samples indicating a possible local 'fresh' DDT source. Mean summation operator PCB (sum of PCB-28, 31, 52, 101, 118, 105, 153, 138, 156, 180, 209) concentration in the Guba Pechenga sediments (12.8 ng/g dry wt.) was significantly higher than in sediments of adjacent areas (2.1 ng/g dry wt.), but it was lower in comparison with summation operator PCB levels reported for the northern Norway harbours and Kola Bay sediments. The highest levels of contaminants were found in sediments collected close to the Liinakhamari harbour. The origin of both PAHs and OCs in the Guba Pechenga sediments is a combination of local sources and long-range transport from lower latitudes.

Ecosystem↗

PubMed2003

Polycyclic aromatic hydrocarbons (PAHs) in bottom sediments of the Kara Sea shelf, Gulf of Ob and Yenisei Bay.

PAH concentration and distribution has been examined in surface sediments samples from the Kara Sea, Russia. The study includes 13 samples from the South-eastern Kara Sea shelf, one sample from the south-western part of the sea, 4 samples from the Baydaratskaya Bay, 5 samples from the Gulf of Ob and 4 samples from the Yenisei Bay, collected in August-September 1993-1994. Cluster analysis and principal component analysis (PCA) were used to identify common patterns and possible sources of PAHs. The total PAH concentration (sum of two- to six-ring aromatic hydrocarbons) in the Kara Sea sediments was generally lower than in the Barents Sea sediments and comparable to the levels in the Pechora and White seas. Two- and three-ring aromatic hydrocarbons predominated in Kara Sea sediments, which indicate a relatively stronger petrogenic origin than that in the adjacent seas. The highest total PAH concentrations within the Kara Sea were found in sediments from the Yenisei Bay and in the South-western part of the Kara Sea in the Eastern Novaya Zemlya Trough. The PAHs of the Yenisei Bay sediments were dominated by perylene and PAHs of petrogenic origin, but had also a strong indication of PAHs of pyrogenic origin. The dominating PAH group in the South-western part of the Kara Sea were four- to six-ring aromatic hydrocarbons, indicating pyrogenic origin. Perylene levels were high in all the Kara Sea samples, and highest levels were found in areas of strong terrigenous influence. The most probable source is decaying peat products being transported to the Kara Sea by both large and small rivers.

Biological Availability↗

PubMed2003

Polychlorinated dibenzofurans/dibenzo-p-dioxins (PCDF/PCDDs) and other dioxin-like substances in marine organisms from the Grenland fjords, S. Norway, 1975-2001: present contamination levels, trends and species specific accumulation of PCDF/PCDD congeners.

Discharge of WHO toxicity equivalents (TEQs) of PCDF/PCDDs to Frierfjorden, Norway has been reduced from an estimated sum of 50-100 kg in the period 1951-1975 to about 6-7 kg in 1976-1990, and further to about 20 g for 1991-2000. In accordance with this, the yearly monitoring since 1987 has shown considerably decreasing contamination in organisms, first highly significant in all indicator species from 1990 to 1991, then levelling off. Present concentrations thus are still high. Compared with estimated "high background" (reference) concentrations of 10 ng TEQ(PCDF/PCDD)/kg w.w. in liver of cod and in hepatopancreas ("brown meat") of crabs, Frierfjord samples in 2001 were about 60 and 70 times higher, respectively. With considerable uncertainty due to large fluctuations, the rate of yearly decrease for TEQ(PCDF/PCDD) in cod liver 1991-2001 has been calculated to 10-12%. A hypothetic target value of 50 ng TEQ/kg w.w. will not be reached until 2015-2020, possibly even later. Including contributions from dioxin-like PCBs and PCNs, the weekly maximum tolerable amount of cod liver and crab hepatopancreas from Frierfjorden in 2001 were about 2-3 g. Multivariate analysis of PCDF/PCDD congener profiles in four fish species, mussels and crabs resulted in five distinct groups, separating four of the species and grouping the remaining two together, hence demonstrating examples of species specific accumulation characteristics.

Animals↗