TY - JOUR
T1 - An overview of millimeter‐wave spectroscopic measurements of chlorine monoxide at Thule, Greenland, February–March, 1992
T2 - Vertical profiles, diurnal variation, and longer‐term trends
AU - de Zafra, R. L.
AU - Emmons, L. K.
AU - Reeves, J. M.
AU - Shindell, D. T.
PY - 1994/6/22
Y1 - 1994/6/22
N2 - Measurements of chlorine monoxide in the stratosphere over Thule, Greenland (76.3N, 68.4W) were made quasi‐continuously during the period February 8 to March 24, 1992, using a high‐sensitivity ground based mm‐wave spectrometer. These observations give diurnal, short term, and long term changes in the mixing ratio and vertical distribution of ClO. At an equivalent time after the Antarctic winter solstice, very large concentrations (up to ∼1.5 ppbv) occur in lower stratospheric ClO, resulting in massive ozone destruction. We saw no evidence for large (∼1 to 1.5 ppbv) amounts of ClO in the 16–25 km range over Thule in February or March, in agreement with UARS (satellite) observations by the MLS mm‐wave spectrometer for this period, and in marked contrast to UARS/MLS and ER‐2 aircraft measurements over northern Europe and eastern Canada, respectively, during January, 1992. We have evidence for smaller enhancements (∼0.2 to 0.5 ppbv) in the 18–30 km range during late February‐early March, which could result from transport of residual low NO2 air following earlier PSC processing (the last of which occurred at least one month earlier, however) or the result of chemical processing by Pinatubo aerosols. Direct influence of Pinatubo aerosols on Arctic ozone during the spring of 1992 has been difficult to assess, and this enhancement of low‐altitude ClO might be a significant indicator of aerosol effects.
AB - Measurements of chlorine monoxide in the stratosphere over Thule, Greenland (76.3N, 68.4W) were made quasi‐continuously during the period February 8 to March 24, 1992, using a high‐sensitivity ground based mm‐wave spectrometer. These observations give diurnal, short term, and long term changes in the mixing ratio and vertical distribution of ClO. At an equivalent time after the Antarctic winter solstice, very large concentrations (up to ∼1.5 ppbv) occur in lower stratospheric ClO, resulting in massive ozone destruction. We saw no evidence for large (∼1 to 1.5 ppbv) amounts of ClO in the 16–25 km range over Thule in February or March, in agreement with UARS (satellite) observations by the MLS mm‐wave spectrometer for this period, and in marked contrast to UARS/MLS and ER‐2 aircraft measurements over northern Europe and eastern Canada, respectively, during January, 1992. We have evidence for smaller enhancements (∼0.2 to 0.5 ppbv) in the 18–30 km range during late February‐early March, which could result from transport of residual low NO2 air following earlier PSC processing (the last of which occurred at least one month earlier, however) or the result of chemical processing by Pinatubo aerosols. Direct influence of Pinatubo aerosols on Arctic ozone during the spring of 1992 has been difficult to assess, and this enhancement of low‐altitude ClO might be a significant indicator of aerosol effects.
UR - https://www.scopus.com/pages/publications/84986401409
U2 - 10.1029/93GL01677
DO - 10.1029/93GL01677
M3 - Article
AN - SCOPUS:84986401409
SN - 0094-8276
VL - 21
SP - 1271
EP - 1274
JO - Geophysical Research Letters
JF - Geophysical Research Letters
IS - 13
ER -