Abstract
Arctic sea routes are opening up for maritime transport due to sea ice retreat leading to increasing human activities in the Arctic and concomitant pressures on the environment. Organotin compounds are used in antifouling paints of large seagoing vessels and are known to leach into the marine environment and accumulate in sediments and biota. As organotin levels in Svalbard sediments have not been documented in peer-reviewed literature before, this study describes the levels in sediment of harbours around Svalbard (Ny-Ålesund, Longyearbyen, Svea, Pyramiden and Barentsburg). Organotin levels in sediments of Svalbard harbours were low (below the detection limit up to 14 ng Sn/g dw sum-butyltin) compared to other Arctic regions with a longer history of shipping. Levels were below known no effect levels and in accordance, no imposex was found in marine whelks from Ny-Ålesund harbour. Of all other analysed compounds in sediments of Kongsfjorden (polycyclic aromatic hydrocarbon (PAHs), polychlorinated biphenyls, polybrominated diphenylethers and perfluorinated compounds) PAH levels were highest and in one sample above action levels. It is advised to continue monitoring contaminant levels, for which the current results form a good basis. If contaminant levels rise, mitigation measures can be taken in time.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Arctic sea routes are opening up for maritime transport due to sea ice retreat. This leads to increasing human activities in the Arctic and concomitant pressures on the environment (Stępień et al. 2014). Local sources of contaminants are closely linked to activities in the area such as shipping, mining and harbour activities and may cause local hotspots of contamination. Contaminants are also transported to the Arctic region from diffuse sources far away by evaporation and air currents, or via rivers and ocean currents (AMAP 1998, 2010), causing widespread contamination of pristine areas, and in particular the marine environment (MacDonald et al. 2000; Letcher et al. 2010; Andersen et al. 2015).
Svalbard is an archipelago in the Barents Sea, bordering the Greenland Sea in the west and the Arctic Ocean in the north, about midway between continental Norway and the North Pole. Svalbard has a few human settlements consisting of the main settlement of Longyearbyen, the Russian mining community of Barentsburg, the historical mining settlement of Pyramiden, the research station of Ny-Ålesund, and the Norwegian mining community of Svea. The main industries on Svalbard are coal mining, tourism, education and research.
Local sources of contamination in Svalbard are a consequence of local settlements, shipping and (historical) coal mining (Kozak et al. 2013). Persistent contaminants such as polycyclic aromatic hydrocarbon (PAHs), polychlorinated biphenyls (PCBs), polybrominated diphenylethers (PBDEs) and perfluorinated compounds (PFCs) are associated with local settlements and coal mining on Svalbard (Hop et al. 2001; Evenset et al. 2006a, 2009). Contaminants related to shipping include air pollution (such as PAHs, fine particles, S and NOx), waste (solid and liquid) and organotin compounds (OTCs), such as tributyltin (TBT; Van Aardenne et al. 2013; Eckhardt et al. 2013; Matthiessen 2013). Organotin compounds are biocides that are added to paint used on ship hulls to prevent hull fouling and thereby decrease drag and fuel consumption (Lindholdt et al. 2015). These anti-fouling compounds leach into the marine environment and have caused shipping-related accumulation of TBT in sediment resulting in the chronic exposure of aquatic organisms (Matthiessen 2013). A well-known effect of TBT exposure is imposex in gastropod molluscs such as marine whelks (Mensink et al. 2002). Imposex is the formation of male characteristics in female snails. It was estimated that about 150 species showed signs of imposex worldwide (Matthiessen et al. 1999). Since the 1960s, TBT has been applied as anti-fouling biocide in paint, until in 2003, the International Maritime Organization (IMO) banned new application of TBT coatings on ships and since 2008 no TBT is allowed to be present on ships (IMO 2001). Not all countries have ratified the treaty yet. In 2012, some 61 contracting states representing 80 % of the worlds tonnage had ratified the treaty (IMO 2012). New input of TBT from TBT-coated ships cannot be excluded in the Arctic in addition to persistent historical TBT pollution. As TBT slowly degrades over time into dibutyltin (DBT) and finally into monobutyltin (MBT), the relative presence of these three compounds can indicate how recent the TBT input was. For this purpose, the Butyltin Degradation Index (BDI) was developed (Diez et al. 2002).
In Ny-Ålesund harbour, imposex has been reported once for the marine snail Buccinum undatum in the mid-1990s (Brick and Bolte 1994). There is, however, no peer-reviewed information available on past or current organotin levels in sediments or biota of Svalbard harbours, nor has imposex been studied further. Organotin contamination and imposex have been studied and identified in other Arctic harbours in Greenland (Jacobsen and Asmund 2000; Strand and Asmund 2003; Strand et al. 2006), Iceland (Skarphédinsdóttir et al. 1996; Svavarsson 2000) and Alaska (Tallmon 2012).
This study focuses on providing insight into organotin contamination of sediments of Svalbard harbours and the occurrence of imposex in marine whelks (Buccinum sp.) of Ny-Ålesund harbour, Kongsfjorden. In addition, levels of other contaminants (PAHs, PCBs, PBDEs and PFCs) were analysed in the sediment of several locations within Kongsfjorden to get a further understanding of local inputs of contaminants in this Svalbard fjord. This will provide a basis to assess pressures and impacts of current and future activities in Svalbard in order to develop relevant and effective mitigation measures in the future.
Materials and methods
Sediment sampling
Sediment in and near harbours of Svalbard was collected in 2009, 2012 and 2013 using a Van Veen grab (Table 1; Fig. 1). In Kongsfjorden (in 2012 and 2013), sediment was sampled at three sites (Ny-Ålesund harbour, Ny-Ålesund Thiisbukta and Kongsfjorden reference). Sampling location Ny-Ålesund Thiisbukta is located in the intertidal part of a bay adjacent to the west of Ny-Ålesund harbour and close to an abandoned waste dump on land. In Kongsfjorden, the upper 5 cm sediment layer from five grabs was mixed and homogenized on board and two subsamples of 200 ml each of this homogenate were stored in pre-rinsed 250-ml glass jars with aluminium foil between sample and lid. Sediment at Ny-Ålesund Thiisbukta was collected directly from shore during low tide. Five sediment surface samples were mixed and homogenized and two subsamples of 200 ml each from this location were stored. In Longyearbyen and Svea (in 2013), sediment from four grabs was mixed and homogenized on board and two subsamples were stored according to the same procedures used in Kongsfjorden. In Pyramiden and Barentsburg (2009) the sampling procedure was slightly different; the upper 0–1 cm from one grab at each sampling station was taken out using a small Plexiglas core and stored directly in pre-cleaned glass jars or polypropylene containers. All sediment samples were frozen to −20 °C immediately after sampling until further analysis.
Sampling of organisms
Nineteen individuals of Buccinum sp. were sampled using baited traps in Ny-Ålesund harbour (near the old coal pier) in July 2013. Snails were kept alive and cool prior to imposex staging. Snails were examined for imposex occurrence using standard procedures (OSPAR Commission 2009).
Chemical analysis
Organotin analysis in sediments consisted of MBT, DBT, TBT, monophenyltin (MPhT), diphenyltin (DPhT) and triphenyltin (TPhT), using an RvA accredited method (Verslycke et al. 2005). In short, tripropyltinchloride was added to the samples as internal standard after which the organotin compounds were extracted by adding methanol, acetic acid and hexane. Compounds were subsequently derivatized using sodium tetraethylborate (4 % in water) after which sodium hydroxide was added to the samples. The hexane layer containing the derivatized compounds was then cleaned by eluting over an aluminium oxide column with pentane. Extracts were concentrated to one ml using a turbovap and subsequently analysed by GC–MS.
PFCs were analysed according to the procedure by Kwadijk et al. (2010). In short, samples were extracted using acetonitrile and cleaned up using hexane and ENVI-Carb. Extracts were analysed using LC–ESI–MS.
PBDEs and PCBs were extracted using the accelerated solvent extraction technique with in-cell clean-up using florisil. Extraction took place over three cycles using a static time of 10 min with a mixture of pentane: dichloromethane (85:15) at 40 °C. Extracts were concentrated to 1 ml.
For PCBs, 1 µl of sample was injected on a Shimadzu GCMS2010 (GC) coupled to a GCMS-QP2010 Ultra (MS) detector (Shimadzu, ‘s Hertogenbosch, the Netherlands). Column used was a 30 m × 0.25 mm i.d. HT8 with a film thickness of 0.25 µm. Detection was performed using electron impact (EI) in single ion monitoring (SIM) mode. Injection port and source temperatures were 250 and 200 °C, respectively. Oven temperature program started at 90 °C, hold for 3 min, increased by 20 °C/min to 170 °C followed by an increase by 2.5 °C/min to 292 °C. At the end of the program, a column was heated to 320 °C for 10 min. The following quantifier and qualifier ions were monitored, respectively, 256 and 258 for PCB 28, 292 and 290 for PCB 52, 326 and 324 for PCB 101, PCB 112 and PCB 118, 360 and 362 for PCB 138 and PCB 153, 394 and 396 for PCB 180. Recovery was typically between 80 and 110 % for all compounds. Calibration curves consisted of nine points within a range of 1–650 ng/ml. R 2 ≥ 0.999 was achieved for each calibration curve for all compounds.
For PBDEs, 1 µl of sample was injected on an Agilent 6890 GC–MS (Agilent, Amstelveen, the Netherlands) using a 50 m × 0.25 mm i.d. CPsil8 column with a film thickness of 0.25 µm. Injection port and source temperatures were 275 and 200 °C, respectively. Oven temperature program started at 90 °C, hold for 3 min, increased by 30 °C/min to 210 °C followed by an increase by 5 °C/min to 290 °C. At the end of the program, a column was heated to 325 °C for 25 min. M/z 79 and 81 were used as quantifier and qualifier ions, respectively. Recovery was typically between 80 and 110 % for all compounds. Calibration curves consisted of nine points within a range of 0.1–500 ng/ml. R 2 ≥ 0.999 was achieved for each calibration curve for all compounds.
PAHs were analysed according to De Boer et al. (2001). In short, PAHs were extracted from the sediments with soxhlet (hexane/acetone 1:1). The extract is concentrated to 10 ml, cleaned over a silica gel–aluminium oxide column and, after addition of 1 ml of acetonitril, concentrated by evaporation to 1 ml of acetonitril. The PAH levels in the acetonitril solution were then analysed by HPLC equipped with fluorescence detection. acenaphthylene was not measured since it was not part of the standard method used for the measurements of PAH in the samples. Naphthalene was excluded from analyses due to fluctuating high background levels in the blanks which would lead to questionable results.
Limit of detection (d limit) was defined as <5 times the method blank or the lowest used calibration point, whichever is highest. Reference materials and method blanks were analysed with each set of samples. All results for blanks and reference materials were within normal limits.
Data treatment
In cases where the TBT concentration was above d limit in a sediment sample, the BDI was calculated as following (Diez et al. 2002):
In case MBT and DBT concentrations were below d limit, the values for these compounds to be included in the calculation were calculated as 0.5 * d limit.
The PAH concentrations were summed as the 16 US EPA PAHs (sum-16-PAH) (naphthalene (Nap), acenaphthylene (Acy), acenaphthene (Ace), fluorene (Fl), phenanthrene (Phe), anthracene (An), fluoranthene (Flu), pyrene (Pyr), benzo[a]anthracene (BaA), chrysene (Chr), benzo[b]fluoranthene (BbF), benzo[k]fluoranthene (BkF), benzo[a]pyrene (BaP), indeno[1,2,3 cd]pyrene (Inp), dibenz[a,h]anthracene (DBA) and benzo[ghi]perylene (BgP). Naphthalene and acenaphthylene were, however, not included in the analysis. The PCB concentrations were presented as sum-7-PCB (PCB-28, PCB-52, PCB-101, PCB-118, PCB-138, PCB-153 and PCB-180).
Results
Organotin concentrations
Organotin concentrations in sediments of Svalbard harbours were low (<d limit—14 ng Sn/g dw; Table 2). MBT and DBT were only detected in Kongsfjorden sediment. TBT was present in 20–67 % of the samples, except for samples from Longyearbyen harbour where no TBT was found above d limit. The highest number of samples with TBT was found in Svea harbour (67 % above d limit), whereas highest sum-butyltin concentrations were found in Ny-Ålesund harbour (<d limit—14 ng Sn/g dw). TPhT was only detected in a single sediment sample of Pyramiden harbour (1.4 ng/g dw), whereas MPhT and DPhT were not detected in any of the sediment samples.
A BDI could be calculated for 13 of the sediment samples with a TBT concentration above d limit (Table 3). The BDI for these samples ranged between 0.4 and 8.3. The BDI was <1 in samples of Pyramiden, Barentsburg, Svea and one sample of Ny-Ålesund. The BDI was >1 for most samples of Ny-Ålesund.
Imposex scores
No imposex was found in females of Buccinum sp. of Ny-Ålesund harbour (Table 4). Of the investigated 19 individuals, three were males and 16 were females.
Other contaminants
The sediment sample collected at Thiisbukta contained the highest sum-16-PAH concentration (17,717 g/g dw), about ten times higher than concentrations in Ny-Ålesund harbour and more than a factor 1000 higher than at the Kongsfjorden reference sites (Table 5). PAH concentrations varied within Ny-Ålesund harbour with sum-16-PAH concentrations being almost two times higher in the sediments around the coal pier of the harbour than in sediments at the commercial pier and further westwards of the coal pier.
PCB concentrations in sediment were low in Kongsfjorden (<d.l.—1.613 ng/g dw sum-7-PCB; Table 6). Highest concentrations were found in Ny-Ålesund harbour (two out of five samples), but there were also concentrations above detection levels at Thiisbukta (one out of one sample) and the reference site (one out of four samples) in Kongsfjorden. All PBDE concentrations in sediment of Kongsfjorden were below d limits. PFC concentrations in sediment of Kongsfjorden were all below d limits, except at one sample at Thiisbukta that contained levels of two PFCs just above detection level (0.2 ng/g perfluorodecane sulphonate (PFDS) dw and 0.2 ng/g perfluorooctane sulphonate (PFOS) dw).
Discussion
Organotin concentrations
Organotin concentrations in sediment of Svalbard harbours were low (<d.l.—14 ng Sn/g dw/24.5 ng kation/g dw for sum-butyltin; 64 % of all sediment samples had all organotin compounds below d limit). TBT levels above d limit varied from 0.3 to 2.9 ng Sn/g dw. Most of the Ny-Ålesund harbour samples (with TBT levels above d limit) had a BDI of >1 suggesting no recent inputs of butyltins in this harbour (Diez et al. 2002), except for one sample with a BDI of 0.8. The latter, however, consisted of a low TBT concentration of 0.3 ng Sn/g dw, and both MBT and DBT concentrations were below d limit. These low concentrations may have resulted in a deviating BDI value, since the other BDI values in Ny-Ålesund harbour were calculated on OTC concentrations mainly above d limit. The few samples of Pyramiden, Barentsburg and Svea with TBT levels above d limits all had a BDI < 1, showing that there may still be some fresh input of TBT in the area. Pyramiden and Barentsburg only had one sediment sample above d limit with a BDI of <1. Svea had four out of six sediment samples above d limit with all showing a BDI of <1. Shipping traffic to Pyramiden is relatively low with only tourist vessels frequenting the area during summer whereas shipping traffic to Barentsburg and Svea is considerably higher with an active coal mine industry at these places. OTC levels in the sediment of another study in Isfjorden (Pyramiden, Longyearbyen, Barentsburg and Colesbukta) confirm low to non-detectable levels of OTC in Svalbard sediments (Evenset et al. 2006a). In this study, two out of 18 sediment samples in 2005 had TBT concentrations above d limit and contained 1.8 ng Sn/g dw (Longyearbyen) and 3.6 ng Sn/g dw (Barentsburg) (Evenset et al. 2006a). Low levels of TBT were explained by seasonally restricted shipping activities around Svalbard due to heavy ice conditions in winter time and a high sedimentation rate, for example in VanMeijenfjord (Svea), covering and diluting sediment concentrations (Cochrane et al. 2001).
Information on OTC concentrations in sediment of Arctic harbours is very limited. In Nuuk harbour, Greenland, sediment concentrations were reported up to 171 ng Sn/g dw for TBT and 180 ng Sn/g dw for sum-butyltin in 1997 (Jacobsen and Asmund 2000). OTCs were not detected in sediment samples of the coastal area of Thule Air Base and Qaanaaq, West Greenland, in 2002 (Strand et al. 2006). This suggests that OTC levels in Arctic sediment are low compared to more populated regions around the world, where the lowest OTC concentrations were reported in the range of up to 27–124 ng Sn/g dw (along the coasts of Italy in 1999–2000, of Japan in 2003, and of Vietnam in 2003; Antizar-Ladislao 2008). Highest TBT concentrations were reported in sediment of an American harbour in 2001–2003 and a Japanese harbour in 2005 (up to 14,000 ng Sn/g dw; Antizar-Ladislao 2008). Even though decreases of OTC concentrations have been reported in water and biota, sediment does not tend to show clear (>20 %) decreasing trends globally since TBT may not be easily broken down in (especially anaerobic) sediment (Matthiessen 2013; Kim et al. 2014).
More information is available on OTC levels in Arctic benthic invertebrates. TBT concentration varied between 0.5 and 4 ng Sn/g ww in Nucella lapillus and 5–65 ng Sn/g ww in Mytilus edulis near Reykjavík harbour in 1993–1994, whereas DBT concentrations fluctuated around 5 ng Sn/g ww in N. lapillus and between 1 and 6 ng Sn/g ww in M. edulis (Skarphédinsdóttir et al. 1996). Concentrations of TBT and degradation products in M. edulis of Nuuk harbour in Greenland were close to 1 ng Sn/g ww in 1997 (Jacobsen and Asmund 2000). At one station in West Greenland, low OTC levels were detected in biota in 2002, in whelks (3.1 ng Sn/g dw sum-butyltin) and clams (11 ng Sn/g dw sum-butyltin; Strand et al. 2006). In other south-western harbours of West Greenland, organotin concentrations were above detection level in biological samples (bivalves) in 66 % of the samples in 1999–2000, with concentrations up to 283 ng/g ww sum-butyltin (Strand and Asmund 2003). In Alaska, evidence of TBT contamination in mussels collected in 2007–2009 was shown in four out of 10 harbours, with a range of 29–54 ng TBT/g ww in mussels at the contaminated harbours (Tallmon 2012). No OTC levels were measured in biota of Svalbard harbours.
All TBT concentrations in the sediment of Svalbard harbours were below the lowest action level of 3 ng Sn/g dw for dredged materials of OSPAR contracting parties (OSPAR Commission 2004; Schipper et al. 2010) and below no observed effect concentrations (NOEC) of 80 ng Sn/g dw (Stronkhorst and Van Hattum 2003).
A field study in Greenland harbours showed that imposex in gastropods may be a more sensitive biomarker for the presence of TBT in the marine environment than the analysis of TBT in sediment or biota samples (Strand et al. 2006). In the gastropod samples collected in Ny-Ålesund harbour in 2013, none of the 16 female specimen showed any stage of imposex. Imposex occurrence has been found in Ny-Ålesund, Kongsfjorden, in marine snail samples of 1992 (Brick and Bolte 1994). At that time, five out of eight female specimen showed signs of imposex. The BDI in Kongsfjorden suggested that no new sources of TBT were presented in Ny-Ålesund harbour. This may be a further sign that OTC concentrations in Ny-Ålesund harbour have decreased over the past two decades and are currently below effect levels in the harbour. However, other Arctic harbours in Alaska and Greenland did show imposex occurrence (Strand et al. 2006; Tallmon 2012). Imposex development occurred in Buccinum sp. in all five sampled harbours in west Greenland in 1999–2000 (Strand and Asmund 2003) and in Buccinum finmarkianum at seven of eight marine stations off Thule Air Base in Northwest Greenland in 2002 (Strand et al. 2006). Nucella lima samples from harbour sites in Alaska in 2007–2009 exhibited imposex, with 36–87.5 % females affected per site (Tallmon 2012). Studies on imposex in the dogwhelks (N. lapillus) in Icelandic waters in 1998 show that levels of imposex have decreased considerably since the early 1990s after banning the use of TBT-containing paints on small vessels (Svavarsson 2000).
Other contaminants
PAHs concentrations were highest of all compounds analysed in Kongsfjorden sediment (1–16,787 ng/g dw), and below lowest European action levels of 2000 ng/g dw for sum-16-PAH for dredged sediment, except for the sediment sample from Thiisbukta (16,787 ng/g dw; OSPAR Commission 2004). The sediment sample of Thiisbukta fell into category 2 (poor/bad) for sum-16-PAH of 2000–20,000 ng/g dw in Norway and were above action level 1 for sum-6-PAH of 1000 ng/g dw in Germany (OSPAR Commission 2004). The sediment sample of Thiisbukta bay consisted of fine sediment with clear black carbon particles which may explain the elevated PAH levels in this sample. In 1997 PAH levels in Kongsfjorden sediment were 927 ng/g dw (Olsson et al. 1998). There are records of several old oil spills in Ny-Ålesund due to leakage from oil tanks or damaged pipes (Skei 1994) with major spills in 1986 and 1990 (Olsson et al. 1998). Additionally, local coal mining related activities may have caused a further input of PAHs into the harbour.
Low levels of PCBs were detected in Kongsfjorden sediments (d.l.—1.6 ng/g sum-7-PCB dw), both in the harbour area and near the dumpsite. Levels are below lowest European action levels of 20 ng/g dw for sum-7-PCB as set for dredged sediment (OSPAR Commission 2004). Low levels of PCBs in Kongsfjorden sediments have been described before in 1991 (0.32 ng/g sum-7-PCB dw; Skei 1994), 1997 (0.07 ng/g sum-7-PCB dw; Olsson et al. 1998) and 2007 (0.17–0.25 ng/g sum-7-PCB dw; Tessmann 2008). Sum-7-PCB concentrations in sediment of other Svalbard fjords were 0.02–3.50 ng/g (Barentsburg), 0.85–4.30 ng/g (Longyearbyen), 0.03–0.82 ng/g (Pyramiden), and 1.84 ng/g (Isfjorden) in September 1998 (Cochrane et al. 2001), 0.70–6.72 ng/g (Barentsburg), 0.16–0.70 ng/g (Longyearbyen) and 1.91–12.4 ng/g (Pyramiden) in 2005 (Evenset et al. 2006a), and 0.10–0.38 ng/g (Longyearbyen), 0.74–5.41 ng/g (Barentsburg) and 1.8–20.2 ng/g (Pyramiden) in 2009 (Evenset et al. 2009). Flux calculations indicated that local sources are important sources outside these settlements (Governor of Svalbard 2008). Elevated levels outside Pyramiden and Barentsburg were probably due to a flooding event in the summer of 2005. High levels of PCB have been measured in soil from these Russian settlements (Jartun et al. 2009), and flood water probably transported contaminated soil to the marine environment.
Other analysed contaminant groups showed levels below d limit in Kongsfjorden sediment, except for the sediment sample at Thiisbukta that showed low levels of PFCs consisting of PFDS and PFOS concentration just above detection level (0.2 ng/g dw). To our knowledge, PFC levels in Kongsfjorden sediment have not been described in peer-reviewed journals before. PFOS concentrations in sediment of Isfjorden varied between 0.10 and 0.54 ng/g dw, whereas sum-PBDE concentrations were between 0.05 and 1.10 ng/g dw in 2005 (Evenset et al. 2006b).
The fact that, of all Kongsfjorden sediment samples, the sampling location at Thiisbukta often showed levels of contaminants above d limit does not come as a surprise. This site is located directly below an old terrestrial garbage dump and may receive contaminants through run-off from the dumpsite area. In a study from 2000/2001 concentrations of PAHs and PCBs in macrobenthos were highest close to the settlement in Kongsfjorden compared to samples taken further out in the fjord, suggesting a local input of these compounds (Hop et al. 2001). Hop et al. (2001) showed that PAH levels in macrobenthos of the main fjords of Svalbard were quite variable both between and within fjords with highest levels in Isfjorden, followed by Grønfjorden, Billefjorden and Adventfjorden, and lowest levels in Kongsfjorden (Hop et al. 2001). Based on the Norwegian guide for classification of fjords, Kongsfjorden macrobenthos was judged insignificantly polluted for PAH (Hop et al. 2001).
Sediment is highly heterogeneous in terms of composition (sediment fractions, organic carbon) and contaminant load as is also shown by this study. Often, a considerable number of sediment samples are needed from each location to obtain an acceptable standard error. In order to get a better insight into contaminant load in sediment and temporal trends of contaminants, a reduction in variance may be achieved by sampling sediments using sediment traps in low turbidity areas. This way mainly freshly transported sediment is sampled giving a more representative picture of the contents and contaminant load of freshly formed sediment layers. However, due to glacial run-off Svalbard fjords such as Kongsfjorden, Isfjorden (including Adventfjorden, Grønfjorden and Billefjord) and VanMijenfjorden receive large amounts of sediment every year (Evenset et al. 2006a, b; Governor of Svalbard 2008). This sediment has a low organic content and some of it will accumulate close to the settlements and thus ‘dilute’ any contaminants that are emitted from the settlements. Therefore, sampling locations should also be carefully selected with knowledge on the sedimentation rates and sources around a settlement.
Future developments
TBT-containing paint has been shown to be highly effective as antifouling paint preventing organisms attaching to ship hulls, thereby preventing the introduction of non-indigenous species and reducing drag on the ship. For the Antarctic region, the best option to prevent the introduction of non-indigenous species is under discussion including the question of whether local sources of TBT contamination may be preferred over the introduction of non-indigenous species with possible catastrophic and non-reversible effects (Lewis et al. 2004). With the predicted increased shipping in the Arctic, the prevention of introduction of invasive species is also a high priority. However, in the meantime, alternative methods to stop fouling have been developed or are under development (for example Müller et al. 2012; Pérez et al. 2016).
Levels of organotin in sediment of Svalbard harbours are currently low and below NOECs based on the results of this study. However, organotin levels below detection level are no guarantee that effects do not occur as TBT may also cause effects below detection level (Strand et al. 2006). A further study on imposex occurrence in all Svalbard harbours may give a more thorough insight into current effects of OTCs in Svalbard.
In the future, with sea ice receding and shipping opportunities in the area rising, more ships may frequent Svalbard shipping lanes and harbours (via the Northern Sea Route and Transpolar Sea Route). As not all countries have ratified the ban on TBT-containing paints for vessels, chances that TBT-containing vessels frequent the area increase. This may result in an elevation of TBT concentrations in areas along shipping lanes and harbours (Ten Hallers-Tjabbes et al. 2003; Schipper et al. 2010). Regular monitoring of sediment organotin concentrations and/or imposex occurrence in gastropods will provide information on organotin trends in the area. If organotin concentrations increase, mitigation is then possible by actively limiting the access of TBT-containing vessels in the Arctic region.
References
AMAP (1998) Assessment report 1998: Arctic pollution issues. Arctic Monitoring and Assessment Programme, Oslo, xii + 859 pp
AMAP (2010) AMAP assessment 2009—persistent organic pollutants (POPs) in the Arctic. Sci Total Environ Special Issue 408:2851–3051
Andersen MS, Fuglei E, König M, Lipasti I, Pedersen ÅØ, Polder A, Yoccoz NG, Routti H (2015) Levels and temporal trends of persistent organic pollutants (POPs) in arctic foxes (Vulpes lagopus) from Svalbard in relation to dietary habits and food availability. Sci Total Environ 511:112–122
Antizar-Ladislao B (2008) Environmental levels, toxicity and human exposure to tributyltin (TBT)-contaminated marine environment. A review. Environ Int 34:292–308
Brick M, Bolte M (1994) Cytology of the outer penis epithelium of Buccinum undatum (L.) from the arctic region—an observation of the imposex phenomenon. Helgoländer Meeresun 48:123–131
Cochrane SJ, Naes K, Carroll J, Trannum HC, Johansen R, Dahle S (2001) Marine environmental assessment of the settlements Barentsburg, Longyaerbyen and Pyramiden in Isfjorden, Svalbard (in Norwegian). Akvaplan-niva report 414-1466, 57 pp
De Boer J, van der Zande TE, Pieters H, Ariese F, Schipper CA, van Brummelen T, Vethaak AD (2001) Organic contaminants and trace metals in flounder liver and sediment from the Amsterdam and Rotterdam harbours and off the Dutch coast. J Environ Monit 3:386–393
Diez S, Abalos M, Bayona JM (2002) Organotin contamination in sediments from the Western Mediterranean enclosures following 10 years of TBT regulation. Water Res 36:905–918
Eckhardt S, Hermansen O, Grythe H, Fiebig M, Stebel K, Cassiani M, Baecklund A, Stohl A (2013) The influence of cruise ship emissions on air pollution in Svalbard—a harbinger of a more polluted Arctic? Atmos Chem Phys 13:8401–8409
Evenset A, Christensen GN, Palerud R (2006a) Contaminants in marine sediments, Isfjorden, Svalbard 2005 (in Norwegian). Akvaplan-niva report 414.3341, 37 pp
Evenset A, Christensen GN, Berger U (2006b) Organochlorines, polybrominated diphenyl ethers and perfluorinated compounds in marine sediments from Isfjorden, Svalbard. Organohalog Compd 68:1458–1461
Evenset A, Christensen GN, Palerud R (2009) Contaminants in marine sediments from Isfjorden, Svalbard 2009: Longyearbyen, Barentsburg, Pyramiden and Coles Bay (in Norwegian). Akvaplan-niva report 4707-1, 134 pp
Governor of Svalbard (2008) PCBs in Svalbard, status of knowledge and management. April 2008. Report 1/2008, 38 pp
Hop H, Sagerup K, Schlabach M, Gabrielsen GW (2001) Persistent organic pollutants in marine macro-benthos near urban settlements in Svalbard; Longyearbyen, Pyramiden, Barentsburg, and Ny-Ålesund. Norwegian Polar Institute report 8, 43 pp
IMO (2001) International convention on the control of harmful anti-fouling systems on ships. AFS convention, London, 5 October 2001
IMO (2012) International convention on the control of harmful anti-fouling systems on ships. Ratification by the United States of America. AFS.1/Circ.49, 21 August 2012
Jacobsen JA, Asmund G (2000) TBT in marine sediments and blue mussels (Mytilus edulis) from central-west Greenland. Sci Total Environ 245:131–136
Jartun M, Ottesen RT, Volden T, Lundkvist Q (2009) Local sources of polychlorinated biphenyls (PCB) in Russian and Norwegian settlements on Spitsbergen Island, Norway. J Toxicol Environ Health Part A 72:284–294
Kim NS, Hong SH, Yim UH, Shin K-H, Shim WJ (2014) Temporal changes in TBT pollution in water, sediment, and oyster from Jinhae Bay after the total ban in South Korea. Mar Pollut Bull 86:547–554
Kozak K, Polkowska Z, Ruman M, Kozioł K, Namieśnik J (2013) Analytical studies on the environmental state of the Svalbard Archipelago provide a critical source of information about anthropogenic global impact. Trends Anal Chem 50:107–126
Kwadijk CJAF, Korytár P, Koelmans AA (2010) Distribution of perfluorinated compounds in aquatic systems in The Netherlands. Environ Sci Technol 44:3746–3751
Letcher RJ, Bustnes JO, Dietz R, Jenssen BM, Jørgensen EH, Sonne C, Verreault J, Vijayan MM, Gabrielsen GW (2010) Exposure and effects assessment of persistent organohalogen contaminants in arctic wildlife and fish. Sci Total Environ 408:2995–3043
Lewis PN, Riddle MJ, Hewitt CL (2004) Management of exogenous threats to Antarctica and the sub-Antarctic Islands: balancing risks from TBT and non-indigenous marine organisms. Mar Pollut Bull 49:999–1005
Lindholdt A, Dam-Johansen K, Olsen SM, Yebra DM, Kiil S (2015) Effects of biofouling development on drag forces of hull coatings for ocean-going ships: a review. J Coat Technol Res 12:415–444
Macdonald RW, Barrie LA, Bidleman TF, Diamond ML, Gregor DJ, Semkin RG, Strachan WMJ, Li YF, Wania F, Alaee M, Alexeeva LB, Backus SM, Bailey R, Bewers JM, Gobeil C, Halsall CJ, Harner T, Hoff JT, Jantunen LMM, Lockhart WL, Mackay D, Muir DCG, Pudykiewicz J, Reimer KJ, Smith JN, Stern GA, Schroeder WH, Wagemann R, Yunker MB (2000) Contaminants in the Canadian Arctic: 5 years of progress in understanding sources, occurrence and pathways. Sci Total Environ 254:93–234
Matthiessen P (2013) Detection, monitoring, and control of tributyltin—an almost complete success story. Environ Toxicol Chem 32:487–489
Matthiessen P, Reynoldson T, Billinghurst Z, Brassard DW, Cameron P, Chandler GT, Davies IM, Horiguchi T, Mount DR, Oehlmann J, Pottinger TG, Sibley PK, Thompson HM, Vethaak AD (1999) Field assessment of endocrine disruption in invertebrates. In: DeFur PL, Crane M, Ingersoll C, Tattersfield L (eds) Endocrine disruption in invertebrates: endocrinology, testing and assessment. SETAC Technical Publication, Pensacola, pp 199–270
Mensink BP, Kralt H, Vethaak AD, Ten Hallers-Tjabbes CC, Koeman JH, van Hattum B, Boon JP (2002) Imposex induction in laboratory reared juvenile Buccinum undatum by tributyltin (TBT). Environ Toxicol Pharmacol 11:49–65
Müller WE, Wang X, Guo YW, Schröder HC (2012) Potentiation of the cytotoxic activity of copper by polyphosphate on biofilm-producing bacteria: a bioinspired approach. Mar Drugs 10:2369–2387
Olsson K, Savinov V, Gulliksen B, Dahle S (1998) Contaminants in marine sediments, Svalbard 1997. Akvaplan-niva Report 414.98.1386, 43 pp
OSPAR Commission (2004) Overview of contracting parties’ national action levels for dredged material. ISBN 1-904426-46-8. http://sednet.org/download/OSPAR_Commission_2004.pdf
OSPAR Commission (2009) JAMP guidelines for contaminant-specific biological effects (OSPAR Agreement 2008-09). Ref. No:2008-9
Pérez M, García M, Ruiz D, Autino JC, Romanelli G, Blustein G (2016) Antifouling activity of green-synthesized 7-hydroxy-4-methylcoumarin. Mar Environ Res 113:134–140
Schipper CA, Rietjens IMCM, Burgess RM, Murk AJ (2010) Application of bioassays in toxicological hazard, risk, and impact assessments of dredged sediments. Mar Pollut Bull 60:2026–2042
Skarphédinsdóttir H, Ólafsdóttir K, Svavarsson J, Jóhannesson T (1996) Seasonal fluctuations of tributyltin (TBT) and dibutyltin (DBT) in the dogwhelk, Nucella lapillus (L.), and the blue mussel, Mytilus edulis L., in Icelandic waters. Mar Pollut Bull 32:358–361
Skei I (1994) Miljøgeokjemiske undersøkelser i Kongsfjorden 1991 og 1992 (Environmental geochemichal survey in Kongsfjorden 1991 and 1992.) Norwegian Institute for Water Research report 0-90112, 42 pp
Stępień A, Koivurova T, Kankaanpää P (2014) The strategic assessment of development of the Arctic: an assessment conducted for the European Union. University of Lapland, Arctic Centre 183 pp
Strand J, Asmund G (2003) Tributyltin accumulation and effects in marine molluscs from West Greenland. Environ Pollut 123:31–37
Strand J, Glahder CM, Asmund G (2006) Imposex occurrence in marine whelks at a military facility in the high Arctic. Environ Pollut 142:98–102
Stronkhorst J, Van Hattum B (2003) Contaminants of concern in Dutch marine harbor sediments. Arch Environ Contam Toxicol 45:306–316
Svavarsson J (2000) Imposex in the Dogwhelk (Nucella lapillus) due to TBT contamination: improvement at high latitudes. Mar Pollut Bull 40:893–897
Tallmon DA (2012) Tributyltin contamination and imposex in Alaska harbors. Bull Environ Contam Toxicol 88:245–249
Ten Hallers-Tjabbes CC, Wegener J-W, Van Hattum BAGM, Kemp JF, Ten Hallers E, Reitsema TJ, Boon JP (2003) Imposex and organotin concentrations in Buccinum undatum and Neptunea antiqua from the North Sea: relationship to shipping density and hydrographical conditions. Mar Environ Res 55:203–233
Tessmann M (2008) Trophic transfer of persistent organic pollutants in the benthic food web of Kongsfjorden, Spitzbergen. Master thesis. Christian-Albrecht-Universität zu Kiel, Germany
van Aardenne J, Colette A, Degraeuwe B, Hammingh P, De Vlieger I (2013) The impact of international shipping on European air quality and climate forcing. EEA Technical Report, Volume 4/2013, 88 p
Verslycke TA, Vethaak AD, Arijs K, Janssen CR (2005) Flame retardants, surfactants and organotins in sediment and mysid shrimp of the Scheldt estuary (The Netherlands). Environ Pollut 136:19–31
Acknowledgements
Captains of the Teisten research vessel of Kings Bay AS in 2012 and 2013 (Ny-Ålesund, Svalbard), Markus Brand (collection of snails), Emiel Brummelhuis (taxonomic identification of snails) and Johan Jol (imposex staging of snails) are highly thanked for their contributions. Carola van Zweeden is kindly thanked for making the map. The reviewers are kindly thanked for further improving the manuscript and Bart van den Heuvel and Anneke van den Brink for the final proof reading. The Wageningen UR TripleP@Sea innovation Program (KB-14-007) is acknowledged for funding this study.
Author information
Authors and Affiliations
Corresponding author
Additional information
This article belongs to the special issue on the ‘Kongsfjorden ecosystem – new views after more than a decade of research’, coordinated by Christian Wiencke and Haakon Hop.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
About this article
Cite this article
van den Heuvel-Greve, M.J., Szczybelski, A.S., van den Brink, N.W. et al. Low organotin contamination of harbour sediment in Svalbard. Polar Biol 39, 1699–1709 (2016). https://doi.org/10.1007/s00300-016-1907-0
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00300-016-1907-0