Affiliations 

  • 1 School of Environmental Science and Natural Resources, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600, UKM Bangi, Selangor, Malaysia. shahrulnadzir@ukm.edu.my
  • 2 School of Environmental and Geographical Science, University of Nottingham Malaysia Campus, Jalan Broga, 43500, Semenyih, Selangor, Malaysia
  • 3 Centre for Tropical Climate Change System (IKLIM), Institute of Climate Change, Universiti Kebangsaan Malaysia, 43600, UKM Bangi, Selangor, Malaysia
  • 4 Centre of Atmospheric Sciences, Chemistry Department, University of Cambridge, Cambridge, CB2 1EW, UK
  • 5 School of Environmental Science and Natural Resources, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600, UKM Bangi, Selangor, Malaysia
  • 6 Centre for Atmospheric Informatics and Emissions Technology, Cranfield University, Cranfield, MK43 0AL, UK
  • 7 Department of Environmental Sciences, Faculty of Environmental Studies, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia
  • 8 National Antarctic Research Centre, IPS Building, University Malaya, 50603, Kuala Lumpur, Malaysia
  • 9 Earth Observation Centre (EOC), Institute of Climate Change, Universiti Kebangsaan Malaysia, 43600, Bangi, Selangor Darul Ehsan, Malaysia
  • 10 Space Science Centre (ANGKASA), Institute of Climate Change Level 5, Research Complex Building, Universiti Kebangsaan Malaysia, 43600, UKM Bangi, Selangor, Malaysia
  • 11 Environmental Health and Industrial Safety Program, School of Diagnostic Science and Applied Health, Faculty of Health Sciences, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300, Kuala Lumpur, Malaysia
  • 12 Biotechnology Faculty of Engineering, Computing and Science Swinburne University of Technology Sarawak Campus (SUTS), 93350, Kuching, Sarawak, Malaysia
  • 13 School of Biological Sciences, Universiti Sains Malaysia, 11800, Penang, Malaysia
  • 14 Sultan Mizan Antarctic Research Foundation, 902-4, Jalan Tun Ismail, 50480, Kuala Lumpur, Malaysia
  • 15 Department of Aquatic Science Faculty of Resource Science & Technology University Malaysia Sarawak, 94300, Kota Samarahan, Sarawak, Malaysia
  • 16 Ecotech Pty. Limited, 1492, Ferntree Gully Road, Knoxfield, VIC, 3180, Australia
Environ Sci Pollut Res Int, 2018 Jan;25(3):2194-2210.
PMID: 29116536 DOI: 10.1007/s11356-017-0521-1

Abstract

The Antarctic continent is known to be an unpopulated region due to its extreme weather and climate conditions. However, the air quality over this continent can be affected by long-lived anthropogenic pollutants from the mainland. The Argentinian region of Ushuaia is often the main source area of accumulated hazardous gases over the Antarctic Peninsula. The main objective of this study is to report the first in situ observations yet known of surface ozone (O3) over Ushuaia, the Drake Passage, and Coastal Antarctic Peninsula (CAP) on board the RV Australis during the Malaysian Antarctic Scientific Expedition Cruise 2016 (MASEC'16). Hourly O3 data was measured continuously for 23 days using an EcoTech O3 analyzer. To understand more about the distribution of surface O3 over the Antarctic, we present the spatial and temporal of surface O3 of long-term data (2009-2015) obtained online from the World Meteorology Organization of World Data Centre for greenhouse gases (WMO WDCGG). Furthermore, surface O3 satellite data from the free online NOAA-Atmospheric Infrared Sounder (AIRS) database and online data assimilation from the European Centre for Medium-Range Weather Forecasts (ECMWF)-Monitoring Atmospheric Composition and Climate (MACC) were used. The data from both online products are compared to document the data sets and to give an indication of its quality towards in situ data. Finally, we used past carbon monoxide (CO) data as a proxy of surface O3 formation over Ushuaia and the Antarctic region. Our key findings were that the surface O3 mixing ratio during MASEC'16 increased from a minimum of 5 ppb to ~ 10-13 ppb approaching the Drake Passage and the Coastal Antarctic Peninsula (CAP) region. The anthropogenic and biogenic O3 precursors from Ushuaia and the marine region influenced the mixing ratio of surface O3 over the Drake Passage and CAP region. The past data from WDCGG showed that the annual O3 cycle has a maximum during the winter of 30 to 35 ppb between June and August and a minimum during the summer (January to February) of 10 to 20 ppb. The surface O3 mixing ratio during the summer was controlled by photochemical processes in the presence of sunlight, leading to the depletion process. During the winter, the photochemical production of surface O3 was more dominant. The NOAA-AIRS and ECMWF-MACC analysis agreed well with the MASEC'16 data but twice were higher during the expedition period. Finally, the CO past data showed the surface O3 mixing ratio was influenced by the CO mixing ratio over both the Ushuaia and Antarctic regions. Peak surface O3 and CO hourly mixing ratios reached up to ~ 38 ppb (O3) and ~ 500 ppb (CO) over Ushuaia. High CO over Ushuaia led to the depletion process of surface O3 over the region. Monthly CO mixing ratio over Antarctic (South Pole) were low, leading to the production of surface O3 over the Antarctic region.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.