Hans Sanderson

Dr. Hans Sanderson

Department of Environmental Science Section of Environmental Chemistry and Toxicology Aarhus University Frederiksborgvej 399, DK-4000 Roskilde, Denmark

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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22 August 2007 in Atmospheric Chemistry and Physics
Verified
Journal Article
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WSWilliam Robert Simpson
William Robert Simpson
RGR. von Glasow
R. von Glasow
KRK. Riedel
K. Riedel
PAP. Anderson
P. Anderson
PAP. Ariya
P. Ariya
EWE. Wolff
E. Wolff
During springtime in the polar regions, unique photochemistry converts inert halide salt ions (e.g. Br−) into reactive halogen species (e.g. Br atoms and BrO) that deplete ozone in the boundary layer to near zero levels. Since their discovery in the late 1980s, research on ozone depletion events (ODEs) has made great advances; however many key processes remain poorly understood. In this article we review the history, chemistry, dependence on environmental conditions, and impacts of ODEs. This research has shown the central role of bromine photochemistry, but how salts are transported from the ocean and are oxidized to become reactive halogen species in the air is still not fully understood. Halogens other than bromine (chlorine and iodine) are also activated through incompletely understood mechanisms that are probably coupled to bromine chemistry. The main consequence of halogen activation is chemical destruction of ozone, which removes the primary precursor of atmospheric oxidation, and generation of reactive halogen atoms/oxides that become the primary oxidizing species. The different reactivity of halogens as compared to OH and ozone has broad impacts on atmospheric chemistry, including near complete removal and deposition of mercury, alteration of oxidation fates for organic gases, and export of bromine into the free troposphere. Recent changes in the climate of the Arctic and state of the Arctic sea ice cover are likely to have strong effects on halogen activation and ODEs; however, more research is needed to make meaningful predictions of these changes.

13 February 2002 in Environmental Science & Technology
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Journal Article
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SLSteve E. Lindberg
Steve E. Lindberg
SBSteve Brooks
Steve Brooks
Che-Jen LinChe-Jen Lin
Che-Jen Lin
KSKaren J. Scott
Karen J. Scott
MLMatthew Landis
Matthew Landis
ARAndreas Richter
Andreas Richter

12 March 2008 in Atmospheric Chemistry and Physics
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Journal Article
Open access
PDF file
ASA. Steffen
A. Steffen
TDT. Douglas
T. Douglas
Marc AmyotMarc Amyot
Marc Amyot
PAP. Ariya
P. Ariya
KAK. Aspmo
K. Aspmo
CTC. Temme
C. Temme
It was discovered in 1995 that, during the spring time, unexpectedly low concentrations of gaseous elemental mercury (GEM) occurred in the Arctic air. This was surprising for a pollutant known to have a long residence time in the atmosphere; however conditions appeared to exist in the Arctic that promoted this depletion of mercury (Hg). This phenomenon is termed atmospheric mercury depletion events (AMDEs) and its discovery has revolutionized our understanding of the cycling of Hg in Polar Regions while stimulating a significant amount of research to understand its impact to this fragile ecosystem. Shortly after the discovery was made in Canada, AMDEs were confirmed to occur throughout the Arctic, sub-Artic and Antarctic coasts. It is now known that, through a series of photochemically initiated reactions involving halogens, GEM is converted to a more reactive species and is subsequently associated to particles in the air and/or deposited to the polar environment. AMDEs are a means by which Hg is transferred from the atmosphere to the environment that was previously unknown. In this article we review Hg research taken place in Polar Regions pertaining to AMDEs, the methods used to collect Hg in different environmental media, research results of the current understanding of AMDEs from field, laboratory and modeling work, how Hg cycles around the environment after AMDEs, gaps in our current knowledge and the future impacts that AMDEs may have on polar environments. The research presented has shown that while considerable improvements in methodology to measure Hg have been made but the main limitation remains knowing the speciation of Hg in the various media. The processes that drive AMDEs and how they occur are discussed. As well, the role that the snow pack and the sea ice play in the cycling of Hg is presented. It has been found that deposition of Hg from AMDEs occurs at marine coasts and not far inland and that a fraction of the deposited Hg does not remain in the same form in the snow. Kinetic studies undertaken have demonstrated that bromine is the major oxidant depleting Hg in the atmosphere. Modeling results demonstrate that there is a significant deposition of Hg to Polar Regions as a result of AMDEs. Models have also shown that Hg is readily transported to the Arctic from source regions, at times during springtime when this environment is actively transforming Hg from the atmosphere to the snow and ice surfaces. The presence of significant amounts of methyl Hg in snow in the Arctic surrounding AMDEs is important because this species is the link between the environment and impacts to wildlife and humans. Further, much work on methylation and demethylation processes has occurred but these processes are not yet fully understood. Recent changes in the climate and sea ice cover in Polar Regions are likely to have strong effects on the cycling of Hg in this environment; however more research is needed to understand Hg processes in order to formulate meaningful predictions of these changes.


1 April 2004 in Regulatory Toxicology and Pharmacology
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Journal Article
Closed access
HSHans Sanderson
Hans Sanderson
DJDavid J Johnson
David J Johnson
TRTamara Reitsma
Tamara Reitsma
RBRichard A Brain
Richard A Brain
CWChristian J Wilson
Christian J Wilson
KSKeith R Solomon
Keith R Solomon

6 February 2004 in Environmental Science & Technology
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Journal Article
Closed access
MGMichael Evan Goodsite
Michael Evan Goodsite
JPJ. M. C. Plane
J. M. C. Plane
Henrik SkovHenrik Skov
Henrik Skov