Publications
Following publications have been announced by our department Matter Transport and Ecosystem Dynamics. For further information please contact Dr Johannes Bieser, author and co-author of the publications:
Slemr, F., Martin, L., Labuschagne, C., Mkololo, T., Angot, H., Magand, O., Dommergue, A., Garat, P., Ramonet, M., & Bieser, J. (2020): Atmospheric mercury in the Southern Hemisphere – Part 1: Trend and inter-annual variations in atmospheric mercury at Cape Point, South Africa, in 2007–2017, and on Amsterdam Island in 2012–2017. Atmos. Chem. Phys., 20, 7683–7692, doi:10.5194/acp-20-7683-2020
Abstract:
The Minamata Convention on Mercury (Hg) entered into force in 2017, committing its 116 parties (as of January 2019) to curb anthropogenic emissions. Monitoring of atmospheric concentrations and trends is an important part of the effectiveness evaluation of the convention. A few years ago (in 2017) we reported an increasing trend in atmospheric Hg concentrations at the Cape Point Global Atmosphere Watch (GAW) station in South Africa (34.3535∘ S, 18.4897∘ E) for the 2007–2015 period. With 2 more years of measurements at Cape Point and the 2012–2017 data from Amsterdam Island (37.7983∘ S, 77.5378∘ E) in the remote southern Indian Ocean, a more complex picture emerges: at Cape Point the upward trend for the 2007–2017 period is still significant, but no trend or a slightly downward trend was detected for the period 2012–2017 at both Cape Point and Amsterdam Island. The upward trend at Cape Point is driven mainly by the Hg concentration minimum in 2009 and maxima in 2014 and 2012. Using ancillary data on 222Rn, CO, O3, CO2, and CH4 from Cape Point and Amsterdam Island, the possible reasons for the trend and its change are investigated. In a companion paper this analysis is extended for the Cape Point station by calculations of source and sink regions using backward-trajectory analysis.
Bieser, J., Angot, H., Slemr, F., & Martin, L. (2020): Atmospheric mercury in the Southern Hemisphere – Part 2: Source apportionment analysis at Cape Point station, South Africa. Atmos. Chem. Phys., 20, 10427–10439, doi:10.5194/acp-20-10427-2020
Abstract:
Mercury (Hg) contamination is ubiquitous. In order to assess its emissions, transport, atmospheric reactivity, and deposition pathways, worldwide Hg monitoring has been implemented over the past 10–20 years, albeit with only a few stations in the Southern Hemisphere. Consequently, little is known about the relative contribution of marine and terrestrial Hg sources, which is important in the context of growing interest in effectiveness evaluation of Hg mitigation policies. This paper constitutes Part 2 of the study describing a decade of atmospheric Hg concentrations at Cape Point, South Africa, i.e. the first long-term (> 10 years) observations in the Southern Hemisphere. Building on the trend analysis reported in Part 1, here we combine atmospheric Hg data with a trajectory model to investigate sources and sinks of Hg at Cape Point. We find that the continent is the major sink, and the ocean, especially its warm regions (i.e. the Agulhas Current), is the major source for Hg.
Further, we find that mercury concentrations and trends from long-range transport are independent of the source region (e.g. South America, Antarctica) and thus indistinguishable. Therefore, by filtering out air masses from source and sink regions we are able to create a dataset representing a southern hemispheric background Hg concentrations. Based on this dataset, we were able to show that the interannual variability in Hg concentrations at Cape Point is not driven by changes in atmospheric circulation but rather due to changes in global emissions (gold mining and biomass burning).
Schreiberová, M., Vlasáková, L., Vlček, O., Šmejdířová, J., Horálek, J., & Bieser, J. (2020): Benzo[a]pyrene in the Ambient Air in the Czech Republic: Emission Sources, Current and Long-Term Monitoring Analysis and Human Exposure. Atmosphere 2020, 11, 955, doi:10.3390/atmos11090955
Abstract:
This paper provides a detailed, thorough analysis of air pollution by benzo[a]pyrene (BaP) in the Czech Republic. The Czech residential sector is responsible for more than 98.8% of BaP, based on the national emission inventory. According to the data from 48 sites of the National Air Quality Monitoring Network, the range of annual average concentration of BaP ranges from 0.4 ng·m−3 at a rural regional station to 7.7 ng·m−3 at an industrial station. Additionally, short-term campaign measurements in small settlements have recorded high values of daily benzo[a]pyrene concentrations (0.1–13.6 ng·m−3) in winter months linked to local heating of household heating. The transboundary contribution to the annual average concentrations of BaP was estimated by the CAMx model to range from 46% to 70% over most of the country. However, the contribution of Czech sources can exceed 80% in residential heating hot spots. It is likely that the transboundary contribution to BaP concentrations was overestimated by a factor of 1.5 due to limitations of the modeling approach used. During the period of 2012–2018, 35–58% of the urban population in the Czech Republic were exposed to BaP concentrations above target. A significant decreasing trend, estimated by the Mann-Kendall test, was found for annual and winter BaP concentrations between 2008 and 2018.
