Krystyna Koziol

Dr. Krystyna Koziol

orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2021 in Science of The Total Environment
Verified
Journal Article
Closed access
FPFilip Pawlak
Filip Pawlak
KKKrystyna Koziol
Krystyna Koziol
ZPZaneta Polkowska
Zaneta Polkowska

24 January 2025 in Environmental Science: Advances
Verified
Journal Article
Open access
PDF file
DMDerek Muir
Derek Muir
María J. GunnarsdóttirMaría J. Gunnarsdóttir
María J. Gunnarsdóttir
KKKrystyna Koziol
Krystyna Koziol
FHFrank A. von Hippel
Frank A. von Hippel
Danuta SzumińskaDanuta Szumińska
Danuta Szumińska
KVKatrin Vorkamp
Katrin Vorkamp
Local sources of persistent organic pollutants (POPs) and Chemicals of Emerging Arctic Concern (CEACs) from use in communities, shipping, and industrial activity contribute to contamination as does long-range environmental transport. Increased human activity in the Arctic as the climate warms may enhance the significance of local sources. Furthermore, climate change may lead to secondary sources of POPs and CEACs from existing reservoirs in the Arctic. This review examines the emerging evidence for releases from these secondary sources of formerly deposited POPs and CEACs as the Arctic climate warms and the potential for future releases with increased infrastructure development and economic activity. Arctic permafrost degradation represents an important source of natural and anthropogenic polycyclic aromatic hydrocarbons (PAHs), and indications exist of releases of POPs related to permafrost thaw, from previous deposition as well as waste sites. Deposition of POPs and some CEACs to Arctic glaciers is relatively well studied while fewer studies explore the impacts of remobilization. Expansion of economic development has the potential for increasing emissions or creating new sources of CEACs in the Arctic. The predicted northward expansion of agriculture, aquaculture, and ship traffic could bring increased emissions of CEACs to northern waters, including pesticides not previously used in the Arctic. Increased industrial chemical use, e.g. fire-fighting foams, flame retardants, lubricant and plastic additives, is likely to occur following the expansion of infrastructure such as airports, seaports, mining, and oil and gas development. While PAHs are relatively well-studied, there is an urgent need for environmental measurements and modelling of emissions of CEACs associated with the expansion of economic activity in the Arctic as well as to predict the future release of legacy POPs from secondary sources, particularly from permafrost.

1 January 2015 in Polar Research
Verified
Journal Article
Open access
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KKKatarzyna Kozak
Katarzyna Kozak
KKKrystyna Koziol
Krystyna Koziol
Bartłomiej LuksBartłomiej Luks
Bartłomiej Luks
SCStanisław Chmiel
Stanisław Chmiel
Marek RumanMarek Ruman
Marek Ruman
Żaneta PolkowskaŻaneta Polkowska
Żaneta Polkowska
The role of atmospheric precipitation in introducing contaminants to the surface waters of the Fuglebekken catchment, Spitsbergen

1 October 2013 in TrAC Trends in Analytical Chemistry
Verified
Journal Article
Closed access
KKKatarzyna Kozak
Katarzyna Kozak
Żaneta PolkowskaŻaneta Polkowska
Żaneta Polkowska
Marek RumanMarek Ruman
Marek Ruman
KKKrystyna Koziol
Krystyna Koziol
JNJacek Namiesnik
Jacek Namiesnik

15 September 2011 in Sensors
Verified
Journal Article
Open access
PDF file
Żaneta PolkowskaŻaneta Polkowska
Żaneta Polkowska
KCKatarzyna Cichala-Kamrowska
Katarzyna Cichala-Kamrowska
Marek RumanMarek Ruman
Marek Ruman
KKKrystyna Koziol
Krystyna Koziol
WKWiesława Ewa Krawczyk
Wiesława Ewa Krawczyk
JNJacek Namiesnik
Jacek Namiesnik
The Fuglebekken basin is situated in the southern part of the island of Spitsbergen (Norwegian Arctic), on the Hornsund fjord (Wedel Jarlsberg Land). Surface water was collected from 24 tributaries (B1–B24) and from the main stream water in the Fuglebekken basin (25) between 10 July 2009 and 30 July 2009. The present investigation reveals the results of the analysis of these samples for their PAH and PCB content. Twelve of 16 PAHs and seven PCBs were determined in the surface waters from 24 tributaries and the main stream. Total PAH and PCB concentrations in the surface waters ranged from 4 to 600 ng/L and from 2 to 400 ng/L respectively. The highest concentrations of an individual PCB (138–308 ng/L and 123 ng/L) were found in samples from tributaries B9 and B5. The presence in the basin (thousands of kilometres distant from industrial centres) of PAHs and PCBs is testimony to the fact that these compounds are transported over vast distances with air masses and deposited in regions devoid of any human pressure.

1 May 2018 in Science of The Total Environment
Verified
Journal Article
Closed access
KKKlaudia Kosek
Klaudia Kosek
KKKatarzyna Kozak
Katarzyna Kozak
KKKrystyna Koziol
Krystyna Koziol
KJKatarzyna Jankowska
Katarzyna Jankowska
SCStanisław Chmiel
Stanisław Chmiel
Żaneta PolkowskaŻaneta Polkowska
Żaneta Polkowska