AIRCRAFT-BORNE DETECTION OF STRATOSPHERIC COLUMN AMOUNTS OF O-3, NO2,OCLO2 CLNO3, HNO3, AND AEROSOLS AROUND THE ARCTIC VORTEX (79-DEGREES-N TO 39-DEGREES-N) DURING SPRING 1993 .1. OBSERVATIONAL DATA
K. Pfeilsticker et al., AIRCRAFT-BORNE DETECTION OF STRATOSPHERIC COLUMN AMOUNTS OF O-3, NO2,OCLO2 CLNO3, HNO3, AND AEROSOLS AROUND THE ARCTIC VORTEX (79-DEGREES-N TO 39-DEGREES-N) DURING SPRING 1993 .1. OBSERVATIONAL DATA, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 102(D9), 1997, pp. 10801-10814
Using several remote sensing techniques on board a research aircraft (
Transall C-160), we measured the stratospheric column amounts of O-3,
NO2, OClO, ClNO3, and HNO3, and the height-resolved aerosol backscatte
ring ratios during March 7-10, 1993. During this period the polar vort
ex extended from the Arctic well into the Mediterranean (35 degrees N)
. Several underflights of the vortex and its edge region were conducte
d, covering Arctic (79 degrees N) to Mediterranean latitudes (39 degre
es N). During all the flights, moderate amounts of NO2 (0.7-2 . 10(15)
/cm(2)), elevated amounts of HNO3 (1.75-2.35 . 10(16)/cm(2)), ClNO3 (2
.4-5.4 . 10(15)/cm(2)),and OClO (6-13 . 10(12)/cm(2)) were found insid
e the vortex, indicating that the air masses of the vortex were still
chemically disturbed. The observation is interpreted as the polar vort
ex going from the stage of its wintertime denoxification (conversion o
f NOx into NOy) and chlorine activation (conversion of HCl and ClNO3 i
nto chlorine oxides) to the springtime reverse processes via the forma
tion of enhanced amounts of ClNO3. In addition, first measurements of
OClO (6.10(12)/cm(2) at solar zenith angle 90 degrees) and high amount
s of ClNO3 (4.10(15)/cm(2)) around 40 degrees N are reported.