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Featured researches published by Jean-Pierre Pommereau.


Journal of Geophysical Research | 1989

Validation of SAGE II ozone measurements

D. M. Cunnold; Joseph M. Zawodny; William P. Chu; Jean-Pierre Pommereau; Florence Goutail; J. Lenoble; M. P. McCormick; Robert E. Veiga; D. Murcray; N. Iwagami; K. Shibasaki; P. C. Simon; W. Peetermans

Stratospheric aerosol and gas experiment (SAGE) II satellite-borne measurements of the stratospheric profiles of NO2 at sunset have been made since October 1984. The measurements are made by solar occultation and are derived from the difference between the absorptions in narrow bandwidth channels centered at 0.448 and 0.453 μm. The precision of the profiles is approximately 5% between an upper altitude of 36 km and a latitude-dependent lower altitude at which the mixing ratio is 4 ppbv (for example, approximately 25 km at mid-latitudes and 29 km in the tropics). At lower altitudes the precision is approximately 0.2 ppbv. The profiles are nominally smoothed over 1 km except at altitudes where the extinction is less than 2×10−5/km. (approximately 38 km altitude), where 5 km smoothing is employed. The profile measurement noise has an autocorrelation distance of 3–5 km for 1 km smoothing and more than 10 km for 5 km smoothing. The absolute accuracy of the measurements is estimated to be 15% based on uncertainties in the absorption cross-sections and their temperature dependence. Comparisons against two sets of balloon profiles and atmospheric trace molecules spectroscopy experiment (ATMOS) measurements show agreement within approximately 10% over the altitude range of 23 to 37 km at mid-latitudes. SAGE II NO2 measurements are calculated to be approximately 20% smaller at the mixing ratio peak than average limb infrared monitor of the stratosphere (LIMS) measurements in the tropics in 1979. They show acceptable agreement with SAGE I sunset NO2 measurements in the tropics in 1979–1981 when the limited resolution and precision of the SAGE I measurements and the differences between the two measurement techniques are considered.


Journal of Geophysical Research | 2008

Validation of Ozone Monitoring Instrument nitrogen dioxide columns

Edward Celarier; Ellen Brinksma; James F. Gleason; J. P. Veefkind; A. Cede; Jay R. Herman; Dimitri V. Ionov; Florence Goutail; Jean-Pierre Pommereau; J.-C. Lambert; M. Van Roozendael; Gaia Pinardi; F. Wittrock; A. Schönhardt; Andreas Richter; Ow Ibrahim; Thomas Wagner; Bojan Bojkov; George H. Mount; E. Spinei; C.M. Chen; Thomas J. Pongetti; Stanley P. Sander; E. J. Bucsela; Mark Wenig; Daan P. J. Swart; H. Volten; M. Kroon; Pieternel F. Levelt

[1] We review the standard nitrogen dioxide (NO2) data product (Version 1.0.), which is based on measurements made in the spectral region 415–465 nm by the Ozone Monitoring Instrument (OMI) on the NASA Earth Observing System-Aura satellite. A number of ground- and aircraft-based measurements have been used to validate the data product’s three principal quantities: stratospheric, tropospheric, and total NO2 column densities under nearly or completely cloud-free conditions. The validation of OMI NO2 is complicated by a number of factors, the greatest of which is that the OMI observations effectively average the NO2 over its field of view (minimum 340 km 2 ), while a ground-based instrument samples at a single point. The tropospheric NO2 field is often very inhomogeneous, varying significantly over tens to hundreds of meters, and ranges from 10 16 cm � 2 over urban and industrial areas. Because of OMI’s areal averaging, when validation measurements are made near NO2 sources the OMI measurements are expected to underestimate the ground-based, and this is indeed seen. Further, we use several different instruments, both new and mature, which might give inconsistent NO2 amounts; the correlations between nearby instruments is 0.8–0.9. Finally, many of the validation data sets are quite small and span a very short length of time; this limits the statistical conclusions that can be drawn from them. Despite these factors, good agreement is generally seen between the OMI and ground-based measurements, with OMI stratospheric NO2 underestimated by about 14% and total and tropospheric columns underestimated by 15–30%. Typical correlations between OMI NO2 and ground-based measurements are generally >0.6.


Journal of Geophysical Research | 1995

Intercomparison of UV/visible spectrometers for measurements of stratospheric NO2 for the Network for the Detection of Stratospheric Change

D. J. Hofmann; Paolo Bonasoni; Martine De Mazière; Franco Evangelisti; Giorgio Giovanelli; Aaron Goldman; Florence Goutail; Jerald W. Harder; R. O. Jakoubek; P. V. Johnston; Jim Kerr; W. Andrew Matthews; Tom Mcelroy; Richard McKenzie; George H. Mount; U. Platt; Jean-Pierre Pommereau; Alain Sarkissian; Paul C. Simon; Susan Solomon; J. Stutz; Alan Thomas; Michel Van Roozendael; Edmund Wu

During the period May 12–23, 1992, seven groups from seven countries met in Lauder, New Zealand, to intercompare their remote sensing instruments for the measurement of atmospheric column NO2 from the surface. The purpose of the intercomparison was to determine the degree of intercomparability and to qualify instruments for use in the Network for the Detection of Stratospheric Change (NDSC). Three of the instruments which took part in the intercomparison are slated for deployment at primary NDSC sites. All instruments were successful in obtaining slant column NO2 amounts at sunrise and sunset on most of the 12 days of the intercomparison. The group as a whole was able to make measurements of the 90° solar zenith angle slant path NO2 column amount that agreed to about ±10% most of the time; however, the sensitivity of the individual measurements varied considerably. Part of the sensitivity problem for these measurements is the result of instrumentation, and part is related to the data analysis algorithms used. All groups learned a great deal from the intercomparison and improved their results considerably as a result of this exercise.


Journal of Geophysical Research | 2006

Latitudinal and vertical distribution of bromine monoxide in the lower stratosphere from Scanning Imaging Absorption Spectrometer for Atmospheric Chartography limb scattering measurements

Christopher E. Sioris; L. J. Kovalenko; Christopher Anthony McLinden; R. J. Salawitch; M. Van Roozendael; Florence Goutail; M. Dorf; K. Pfeilsticker; Kelly Chance; C. von Savigny; X. Liu; Thomas P. Kurosu; Jean-Pierre Pommereau; H. Bösch; J. Frerick

[1] Vertical profiles of stratospheric bromine monoxide (BrO) in the 15–30 km range are retrieved from SCIAMACHY limb scatter data over the globe. First validation comparisons with the balloon-borne SAOZ-BrO and LPMA/DOAS instruments indicate retrieval biases of � 20% or less. Propagated spectral fitting uncertainties lead to a precision approaching � 25% on a 2 km grid at 25 km. This worsens at higher altitudes because of reduced signal and at lower altitudes because of the reduced penetrability of the atmosphere. In terms of volume mixing ratio (VMR), the single profile precision increases from � 4 pptv at 17 km to � 8 pptv at 27 km. Repeatability, an alternative indicator of precision, is 2–3 pptv for SCIAMACHY retrievals and independent of altitude. The BrO stratospheric number density peak generally lies 5 ± 2 km above the tropopause. In the tropics, the stratospheric BrO VMR generally increases with increasing altitude. The observed stratospheric BrO global distribution is generally consistent with previous balloon measurements but does not agree well with results of a model that uses Bry inferred only from the observed breakdown of long-lived bromoalkanes (i.e., methyl bromide and halons). We find best agreement with the observed vertical and latitudinal distribution of BrO for model results that include an 8.4 ± 2 pptv contribution to stratospheric Bry, most of which is expected from the breakdown of VSL (very short lived) bromocarbons, in addition to the � 16 pptv contribution from longer-lived sources. This suggests that stratospheric Bry exceeds 20 pptv. Profiles of Bry profiles derived from the balloon measurements of BrO also suggest Bry is in excess of 20 pptv, but the uncertainty and variability of these results do not allow us to definitively rule out this concentration. We find typical BrO VMRs of � 4 pptv at 15 km in the tropical tropopause layer, suggesting that a significant portion of the bromine from VSL bromoalkane sources may be carried across the tropopause in the form of inorganic decomposition products. We discuss a variety of VSL bromocarbons species that may be contributing to the elevated concentrations of stratospheric BrO.


Journal of the Atmospheric Sciences | 1999

Investigation of Pole-to-Pole Performances of Spaceborne Atmospheric Chemistry Sensors with the NDSC

J.-C. Lambert; Michel Van Roozendael; Martine De Mazière; Paul C. Simon; Jean-Pierre Pommereau; Florence Goutail; Alain Sarkissian; James F. Gleason

Abstract Spaceborne atmospheric chemistry sensors provide unique access to the distribution and variation of the concentration of many trace species on the global scale. However, since the measurements and the retrieval algorithms are sensitive to a variety of instrumental as well as atmospheric sources of error, they need to be validated carefully by correlative measurements. The quality control and validation of satellite measurements on the global scale, as well as in the long term, is one of the goals of the Network for the Detection of Stratospheric Change (NDSC). Started in 1991, at the present time the NDSC includes five primary and two dozen complementary stations distributed from the Arctic to the Antarctic, comprising a variety of instruments such as UV–visible spectrometers, Fourier transform infrared spectrometers, lidars, and millimeter-wave radiometers. After an overview of the main sources of uncertainty which could perturb the measurements from space, and of the ground-based data provided ...


Geophysical Research Letters | 1994

Ozone and nitrogen dioxide vertical distributions by uv-visible solar occultation from balloons

Jean-Pierre Pommereau; Jacques Piquard

A light and easily handled balloon-borne uv-visible spectrometer was designed for investigating ozone photochemistry in the Arctic winter. The optical sonde was flown 10 times during the EASOE campaign at Kiruna in Northern Sweden from November 1991 until March 1992. The flights gave the first simultaneous measurements of the vertical distributions of ozone and nitrogen dioxide in the Arctic winter.


Advances in Space Research | 1999

Network science landers for Mars

A.-M. Harri; O. Marsal; P. Lognonné; G.W. Leppelmeier; Tilman Spohn; Karl-Heinz Glassmeier; F. Angrilli; W. B. Banerdt; J. P. Barriot; J.J. Berthelier; Simon B. Calcutt; J.C. Cerisier; David Crisp; Véronique Dehant; Domenico Giardini; R. Jaumann; Y. Langevin; Michel Menvielle; G. Musmann; Jean-Pierre Pommereau; S. Di Pippo; D. Guerrier; K. Kumpulainen; Soren E. Larsen; Antoine Mocquet; Jouni Polkko; J. Runavot; W. Schumacher; T. Siili; J. Simola

Abstract The NetLander Mission will deploy four landers to the Martian surface. Each lander includes a network science payload with instrumentation for studying the interior of Mars, the atmosphere and the subsurface, as well as the ionospheric structure and geodesy. The NetLander Mission is the first planetary mission focusing on investigations of the interior of the planet and the large-scale circulation of the atmosphere. A broad consortium of national space agencies and research laboratories will implement the mission. It is managed by CNES (the French Space Agency), with other major players being FMI (the Finnish Meteorological Institute), DLR (the German Space Agency), and other research institutes. According to current plans, the NetLander Mission will be launched in 2005 by means of an Ariane V launch, together with the Mars Sample Return mission. The landers will be separated from the spacecraft and targeted to their locations on the Martian surface several days prior to the spacecrafts arrival at Mars. The landing system employs parachutes and airbags. During the baseline mission of one Martian year, the network payloads will conduct simultaneous seismological, atmospheric, magnetic, ionospheric, geodetic measurements and ground penetrating radar mapping supported by panoramic images. The payloads also include entry phase measurements of the atmospheric vertical structure. The scientific data could be combined with simultaneous observations of the atmosphere and surface of Mars by the Mars Express Orbiter that is expected to be functional during the NetLander Missions operational phase. Communication between the landers and the Earth would take place via a data relay onboard the Mars Express Orbiter.


Geophysical Research Letters | 1994

An overview of the EASOE Campaign

J. A. Pyle; N. R. P. Harris; J. C. Farman; F. Arnold; G. O. Braathen; R. A. Cox; P. Faucon; Roderic L. Jones; G. Mégie; A. O'Neill; U. Platt; Jean-Pierre Pommereau; Ulrich Schmidt; Frode Stordal

The scientific planning of the EASOE campaign is outlined and the various constituent and meteorological data sets are described.


Applied Optics | 2000

SALOMON: a new, light balloonborne UV–visible spectrometer for nighttime observations of stratospheric trace-gas species

Jean-Baptiste Renard; Michel Chartier; C. Robert; Gilles Chalumeau; Gwenaël Berthet; Michel Pirre; Jean-Pierre Pommereau; Florence Goutail

A new, light balloonborne UV-visible spectrometer, called SALOMON, is designed to perform nighttime measurements of stratospheric trace-gas species by using the Moon as a light source. The first flight, performed on 31 October 1998 at mid-latitude with a float altitude of 26.7 km, allowed the performance of the pointing system to be checked and vertical profiles of ozone, NO(2), NO(3), and possibly OBrO to be obtained. First the instrument and then the performance of the pointing system and the detector are described. Finally the vertical profiles are compared with other profiles obtained at the same location five years before with the heavier balloonborne spectrometer AMON, which uses a star as the light source.


Geophysical Research Letters | 1994

Observations of the vertical distribution of stratospheric OClO

Jean-Pierre Pommereau; Jacques Piquard

A light and easily operated balloon-borne UV-visible spectrometer was designed for investigating ozone chemistry in the Arctic winter. The optical sonde was flown 10 times during EASOE in northern Scandinavia in winter 1991–92 to measure O3 and NO2, the results of which are presented in a companion paper. On two occasions, 13 and 16 January 1992, during the coldest period of the campaign, when PSCs were visible from the ground, OClO mixing ratios of 16 ± 2 and 19 ± 3 ppt (1 s.d.) respectively were detected around 20 km at sunset. These are the first OClO profiles to be reported. They yield integrated columns of 5.8 and 8.9 1012 mol./cm² above 16 km and 17 km respectively. These values are consistent with ground-based and aircraft total column measurements in the Arctic.

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Dive into the Jean-Pierre Pommereau's collaboration.

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Florence Goutail

Centre national de la recherche scientifique

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Andrea Pazmino

Centre national de la recherche scientifique

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Michel Van Roozendael

Belgian Institute for Space Aeronomy

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Anne Garnier

Centre national de la recherche scientifique

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F. Hendrick

Belgian Institute for Space Aeronomy

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Franck Lefèvre

Centre national de la recherche scientifique

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Sergey Khaykin

Université Paris-Saclay

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M. Van Roozendael

Belgian Institute for Space Aeronomy

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