Distributions and recent changes of carbon monoxide in the lower troposphere
- 20 August 1998
- journal article
- Published by American Geophysical Union (AGU) in Journal of Geophysical Research: Atmospheres
- Vol. 103 (D15) , 19015-19033
- https://doi.org/10.1029/98jd01366
Abstract
Since 1988, the distribution of carbon monoxide (CO) in the lower troposphere has been determined using a globally distributed air sampling network. Site locations range from 82°N to 90°S, with wide longitudinal coverage, and represent the marine boundary layer, regionally polluted atmospheres, and the free troposphere. These measurements present a unique, intercalibrated, and internally consistent data set that are used to better define the global temporal and spatial distribution of CO. In this paper, times series from 49 sites are discussed. With an average lifetime of ∼2 months, CO showed significant concentration gradients. In the marine boundary layer, mixing ratios were greatest in the northern winter (200–220 ppb) and lowest in the southern summer (35–45 ppb). The interhemispheric gradient showed strong seasonality with a maximum difference between the high latitudes of the northern and southern hemispheres (160–180 ppb) in February and March and a minimum in July and August (10–20 ppb). Higher CO was found in regions near human development relative to those over more remote areas. The distributions provide additional evidence of the widespread pollution of the lower atmosphere. Remote areas in the high northern hemisphere are polluted by anthropogenic activities in the middle latitudes, and those in the southern hemisphere are heavily influenced by the burning of biomass in the tropics. While tropospheric concentrations of CO exhibit periods of increase and decrease, the globally averaged CO mixing ratio over the period from 1990 through 1995 decreased at a rate of approximately 2 ppb yr−1.This publication has 48 references indexed in Scilit:
- An internally consistent set of globally distributed atmospheric carbon monoxide mixing ratios developed using results from an intercomparison of measurementsJournal of Geophysical Research: Atmospheres, 1998
- Transport‐induced interannual variability of carbon monoxide determined using a chemistry and transport modelJournal of Geophysical Research: Atmospheres, 1996
- Changes in CH4 and CO growth rates after the eruption of Mt. Pinatubo and their link with changes in tropical tropospheric UV fluxGeophysical Research Letters, 1996
- On the effects of stratospheric circulation changes on trace gas trendsJournal of Geophysical Research: Atmospheres, 1994
- Interannual variability over the eastern North Atlantic Ocean: Chemical and meteorological evidence for tropical influence on regional‐scale transport in the extratropicsJournal of Geophysical Research: Atmospheres, 1994
- Evidence for interannual variability of the carbon cycle from the National Oceanic and Atmospheric Administration/Climate Monitoring and Diagnostics Laboratory Global Air Sampling NetworkJournal of Geophysical Research: Atmospheres, 1994
- The growth rate and distribution of atmospheric methaneJournal of Geophysical Research: Atmospheres, 1994
- Concentration and 13C records of atmospheric methane in New Zealand and Antarctica: Evidence for changes in methane sourcesJournal of Geophysical Research: Atmospheres, 1994
- Reevaluation of the NOAA/CMDL carbon monoxide reference scale and comparisons with CO reference gases at NASA‐Langley and the Fraunhofer InstitutJournal of Geophysical Research: Atmospheres, 1994
- Net yield of OH, CO, and O3 from the oxidation of atmospheric methaneAtmospheric Environment. Part A. General Topics, 1992