Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
Environ Sci Pollut Res Int
2017 Jun 01;2416:14218-14233. doi: 10.1007/s11356-017-8851-6.
Show Gene links
Show Anatomy links
Response of marine benthic fauna to thin-layer capping with activated carbon in a large-scale field experiment in the Grenland fjords, Norway.
Samuelsson GS
,
Raymond C
,
Agrenius S
,
Schaanning M
,
Cornelissen G
,
Gunnarsson JS
.
???displayArticle.abstract???
A field experiment with thin-layer capping was conducted in the Grenland fjords, Norway, for remediation in situ of mercury and dioxin-contaminated sediments. Experimental fields at 30 and 95 m depth were capped with (i) powdered activated carbon (AC) mixed with clay (AC+cla`y), (ii) clay, and (iii) crushed limestone. Ecological effects on the benthic community and species-feeding guilds were studied 1 and 14 months after capping, and a total of 158 species were included in the analyses. The results show that clay and limestone had only minor effects on the benthic community, while AC+clay caused severe perturbations. AC+clay reduced the abundance, biomass, and number of species by up to 90% at both 30 and 95 m depth, and few indications of recovery were found during the period of this investigation. The negative effects of AC+clay were observed on a wide range of species with different feeding strategies, although the suspension feeding brittle star Amphiura filiformis was particularly affected. Even though activated carbon is effective in reducing sediment-to-water fluxes of dioxins and other organic pollutants, this study shows that capping with powdered AC can lead to substantial disturbances to the benthic community.
Fig. 1.
a The Grenland fjords are located in south-eastern Norway. b The magnesium smelter (pollutant source) was situated in the inner part of the fjord system, nearby the mouth of the Skien River. c The experimental fields at 30 m are located in the Ormerfjord, and d the fields at 80–95 m depth are located in the Eidangerfjord
Fig. 2. Similarities and dissimilarities in the macrobenthic community in a dendrogram for hierarchical cluster analysis at 30 m depth (group average linking), b ordination plot (n-MDS) at 30 m depth, and c ordination plot (n-MDS) at 80–95 m depth
Fig. 3. Organisms sorted in feeding guilds and taxonomic groups in: a number of species per sample at 30 m, b number of species per sample at 80–95 m, c organism abundance per square meter at 30 m, d organism abundance per square meter at 80–95 m, e biomass (g wet weight) per square meter at 30 m, f biomass (g wet weight) per square meter at 80–95 m. Mean ± SE, month 1 n = 3, month 14 n = 5
Beckingham,
Observations of limited secondary effects to benthic invertebrates and macrophytes with activated carbon amendment in river sediments.
2013, Pubmed
Beckingham,
Observations of limited secondary effects to benthic invertebrates and macrophytes with activated carbon amendment in river sediments.
2013,
Pubmed
Beckingham,
Field-scale reduction of PCB bioavailability with activated carbon amendment to river sediments.
2011,
Pubmed
Cho,
Field methods for amending marine sediment with activated carbon and assessing treatment effectiveness.
2007,
Pubmed
Cho,
Field application of activated carbon amendment for in-situ stabilization of polychlorinated biphenyls in marine sediment.
2009,
Pubmed
Cornelissen,
Large-scale field study on thin-layer capping of marine PCDD/F-contaminated sediments in Grenlandfjords, Norway: physicochemical effects.
2012,
Pubmed
Cornelissen,
A large-scale field trial of thin-layer capping of PCDD/F-contaminated sediments: Sediment-to-water fluxes up to 5 years post-amendment.
2016,
Pubmed
Cornelissen,
Remediation of contaminated marine sediment using thin-layer capping with activated carbon--a field experiment in Trondheim harbor, Norway.
2011,
Pubmed
Cornelissen,
Extensive sorption of organic compounds to black carbon, coal, and kerogen in sediments and soils: mechanisms and consequences for distribution, bioaccumulation, and biodegradation.
2005,
Pubmed
Ghosh,
In-situ sorbent amendments: a new direction in contaminated sediment management.
2011,
Pubmed
Janssen,
Assessment of field-related influences on polychlorinated biphenyl exposures and sorbent amendment using polychaete bioassays and passive sampler measurements.
2011,
Pubmed
Janssen,
Biological responses to activated carbon amendments in sediment remediation.
2013,
Pubmed
Janssen,
Assessment of nontoxic, secondary effects of sorbent amendment to sediments on the deposit-feeding organism Neanthes arenaceodentata.
2012,
Pubmed
Jonker,
Ecotoxicological effects of activated carbon addition to sediments.
2009,
Pubmed
Jonker,
Effects of sedimentary sootlike materials on bioaccumulation and sorption of polychlorinated biphenyls.
2004,
Pubmed
Josefsson,
Capping efficiency of various carbonaceous and mineral materials for in situ remediation of polychlorinated dibenzo-p-dioxin and dibenzofuran contaminated marine sediments: sediment-to-water fluxes and bioaccumulation in boxcosm tests.
2012,
Pubmed
Knutzen,
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.
2003,
Pubmed
Kupryianchyk,
Ecotoxicological effects of activated carbon amendments on macroinvertebrates in nonpolluted and polluted sediments.
2011,
Pubmed
Kupryianchyk,
In situ treatment with activated carbon reduces bioaccumulation in aquatic food chains.
2013,
Pubmed
Kupryianchyk,
Long-term recovery of benthic communities in sediments amended with activated carbon.
2012,
Pubmed
Kupryianchyk,
Bioturbation and dissolved organic matter enhance contaminant fluxes from sediment treated with powdered and granular activated carbon.
2013,
Pubmed
Lillicrap,
Assessment of the direct effects of biogenic and petrogenic activated carbon on benthic organisms.
2015,
Pubmed
Lin,
Bioturbation delays attenuation of DDT by clean sediment cap but promotes sequestration by thin-layered activated carbon.
2014,
Pubmed
Lohrer,
Bioturbators enhance ecosystem function through complex biogeochemical interactions.
2004,
Pubmed
McLeod,
Biological uptake of polychlorinated biphenyls by Macoma balthica from sediment amended with activated carbon.
2007,
Pubmed
McLeod,
Biodynamic modeling of PCB uptake by Macoma balthica and Corbicula fluminea from sediment amended with activated carbon.
2008,
Pubmed
Millward,
Addition of activated carbon to sediments to reduce PCB bioaccumulation by a polychaete (Neanthes arenaceodentata) and an amphipod (Leptocheirus plumulosus).
2005,
Pubmed
Nybom,
Effects of activated carbon ageing in three PCB contaminated sediments: Sorption efficiency and secondary effects on Lumbriculus variegatus.
2015,
Pubmed
Nybom,
Responses of Lumbriculus variegatus to activated carbon amendments in uncontaminated sediments.
2012,
Pubmed
Rakowska,
In situ remediation of contaminated sediments using carbonaceous materials.
2012,
Pubmed
Samuelsson,
Capping in situ with activated carbon in Trondheim harbor (Norway) reduces bioaccumulation of PCBs and PAHs in marine sediment fauna.
2015,
Pubmed
Worm,
Impacts of biodiversity loss on ocean ecosystem services.
2006,
Pubmed
Zimmerman,
Effects of dose and particle size on activated carbon treatment to sequester polychlorinated biphenyls and polycyclic aromatic hydrocarbons in marine sediments.
2005,
Pubmed
Zimmerman,
Addition of carbon sorbents to reduce PCB and PAH bioavailability in marine sediments: physicochemical tests.
2004,
Pubmed