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Novelli et al. 1992
Novelli, P.C., Steele, L.P. and Tans, P.P. (1992). Mixing ratios of carbon monoxide in the troposphere. Journal of Geophysical Research 97. doi: 10.1029/92JD02010. issn: 0148-0227.

Carbon monoxide (CO) mixing ratios were measured in air samples collected weekly at eight locations. The air was collected as part of the CMDL/NOAA cooperative flask sampling program (Climate Monitoring and Diagnositics Laboratory, formerly Geophysical Monitoring of Climatic Change, Air Resources Laboratory/National Oceanic and Atmospheric Administration) at Point Barrow, Alaska (71¿N), Niwot Ridge, Colorado (40¿N), Mauna Loa and Cape Kumakahi, Hawaii (19¿N), Guam, Marianas Islands (13¿N), Christmas Island (2¿N), Ascension Island (8¿S) and American Samoa (14¿S). Half-liter or 3-L glass flasks fitted with glass piston stopcocks holding teflon O rings were used for sample collection. CO levels were determined within several weeks of collection using gas chromatography followed by mercuric oxide reduction detection, and mixing ratios were referenced against the CMDL/NOAA carbon monoxide standard scale. During the period of study (mid-1988 through December 1990) CO levels were greatest in the high latitudes of the northern hemisphere (mean mixing ratio from January 1989 to December 1990 at Point Barrow was approximately 154 ppb) and decreased towards the south (mean mixing ratio at Samoa over a similar period was 65 ppb.

Mixing ratios varied seasonally, the amplitude of the seasonal cycle was greatest in north and decreased to the south. Carbon monoxide levels were affected by both local and regional scale processes. The difference in CO levels between northern and southern latitudes also varied seasonally. The greatest difference in CO mixing ratios between Barrow and Samoa was observed during the northern winter (about 150 ppb). The smallest difference, 40 ppb, occurred during the austral winter. The annually averaged CO difference between 71¿N and 14¿S was approximately 90 ppb in both 1989 and 1990; the annually averaged interhemispheric gradient from 71¿N to 41¿S is estimated as approximately 95 ppb. ¿American Geophysical Union 1992

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Abstract

Keywords
Atmospheric Composition and Structure, Troposphere—composition and chemistry, Atmospheric Composition and Structure, Geochemical cycles, Atmospheric Composition and Structure, General or miscellaneous, Atmospheric Composition and Structure, Pollution—urban and regional
Journal
Journal of Geophysical Research
http://www.agu.org/journals/jb/
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American Geophysical Union
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