
Understanding trends in stratospheric NO y and NO 2
Author(s) -
McLinden C. A.,
Olsen S. C.,
Prather M. J.,
Liley J. B.
Publication year - 2001
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2000jd000100
Subject(s) - ozone layer , sunset , sunrise , ozone depletion , stratosphere , environmental science , atmospheric sciences , ozone , atmospheric chemistry , twilight , halogen , nitrogen , nitrous oxide , zenith , meteorology , chemistry , geography , physics , alkyl , remote sensing , organic chemistry , astronomy
Nitrous oxide (N 2 O), an important greenhouse gas, has been increasing since 1980 at a rate of about +3% per decade. Recently, a notably greater rate of increase of about +5% per decade since 1980 was reported for measurements of stratospheric nitrogen dioxide (NO 2 ) over Lauder, New Zealand. Since N 2 O is the dominant source of odd‐nitrogen compounds in the stratosphere, including NO 2 , this presents an obvious conundrum. Analysis here shows that these apparently conflicting trends are generally consistent when viewed in a global‐change framework, specifically, when concurrent trends in stratospheric ozone and halogens are included. Using a combination of photochemical and three‐dimensional chemistry‐transport models, we predict a 1980–2000 trend in the NO 2 , as measured over Lauder, New Zealand, of +4.3%/decade when these concurrent trends are considered. Of this, only +2.4%/decade is attributed directly to the increase in N 2 O; the remainder includes +2.5%/decade due to the ozone change and −0.6%/decade to the increased halogens' impact on odd‐nitrogen partitioning. The slant column densities of NO 2 , as measured from the zenith scattered sunlight during twilight, are found to (1) overestimate the trend by +0.4%/decade as compared to the true vertical column densities and (2) display a diurnally varying trend with a maximum during the night and large gradients through sunrise and sunset in good agreement with measurement. Nonetheless, measurements such as these are essential for identifying global change and provide a lesson in understanding it: careful simulation of the time, location, and geometry of measurements must be combined with concurrent trends in related chemical species and climate parameters.