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Dive into the research topics where Lieven Clarisse is active.

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Featured researches published by Lieven Clarisse.


Bulletin of the American Meteorological Society | 2012

Hyperspectral Earth Observation from IASI: Five Years of Accomplishments

Fiona Hilton; Raymond Armante; Thomas August; Christopher D. Barnet; Aurélie Bouchard; C. Camy-Peyret; Virginie Capelle; Lieven Clarisse; Cathy Clerbaux; Pierre-François Coheur; Andrew Collard; Cyril Crevoisier; G. Dufour; David P. Edwards; François Faijan; Nadia Fourrié; Antonia Gambacorta; Mitchell D. Goldberg; Vincent Guidard; Daniel Hurtmans; Sam Illingworth; Nicole Jacquinet-Husson; Tobias Kerzenmacher; Dieter Klaes; L. Lavanant; Guido Masiello; Marco Matricardi; A. P. McNally; Stuart M. Newman; Edward Pavelin

The Infrared Atmospheric Sounding Interferometer (IASI) forms the main infrared sounding component of the European Organisation for the Exploitation of Meteorological Satellitess (EUMETSATs) Meteorological Operation (MetOp)-A satellite (Klaes et al. 2007), which was launched in October 2006. This article presents the results of the first 4 yr of the operational IASI mission. The performance of the instrument is shown to be exceptional in terms of calibration and stability. The quality of the data has allowed the rapid use of the observations in operational numerical weather prediction (NWP) and the development of new products for atmospheric chemistry and climate studies, some of which were unexpected before launch. The assimilation of IASI observations in NWP models provides a significant forecast impact; in most cases the impact has been shown to be at least as large as for any previous instrument. In atmospheric chemistry, global distributions of gases, such as ozone and carbon monoxide, can be produ...


Philosophical Transactions of the Royal Society B | 2013

Towards a climate-dependent paradigm of ammonia emission and deposition

Mark A. Sutton; Stefan Reis; Stuart N. Riddick; U. Dragosits; E. Nemitz; Mark R. Theobald; Y. Sim Tang; Christine F. Braban; Massimo Vieno; Anthony J. Dore; Sarah Wanless; Francis Daunt; D. Fowler; Trevor D. Blackall; C. Milford; Chris Flechard; Benjamin Loubet; Raia Silvia Massad; Pierre Cellier; Erwan Personne; Pierre-François Coheur; Lieven Clarisse; Martin Van Damme; Yasmine Ngadi; Cathy Clerbaux; Carsten Ambelas Skjøth; Camilla Geels; Ole Hertel; Roy Wichink Kruit; Robert W. Pinder

Existing descriptions of bi-directional ammonia (NH3) land–atmosphere exchange incorporate temperature and moisture controls, and are beginning to be used in regional chemical transport models. However, such models have typically applied simpler emission factors to upscale the main NH3 emission terms. While this approach has successfully simulated the main spatial patterns on local to global scales, it fails to address the environment- and climate-dependence of emissions. To handle these issues, we outline the basis for a new modelling paradigm where both NH3 emissions and deposition are calculated online according to diurnal, seasonal and spatial differences in meteorology. We show how measurements reveal a strong, but complex pattern of climatic dependence, which is increasingly being characterized using ground-based NH3 monitoring and satellite observations, while advances in process-based modelling are illustrated for agricultural and natural sources, including a global application for seabird colonies. A future architecture for NH3 emission–deposition modelling is proposed that integrates the spatio-temporal interactions, and provides the necessary foundation to assess the consequences of climate change. Based on available measurements, a first empirical estimate suggests that 5°C warming would increase emissions by 42 per cent (28–67%). Together with increased anthropogenic activity, global NH3 emissions may increase from 65 (45–85) Tg N in 2008 to reach 132 (89–179) Tg by 2100.


Geophysical Research Letters | 2010

A correlation method for volcanic ash detection using hyperspectral infrared measurements

Lieven Clarisse; Fred Prata; Jean Lionel Lacour; Daniel Hurtmans; Cathy Clerbaux; Pierre-François Coheur

Remote satellite detection of airborne volcanic ash is important for mitigating hazards to aviation and for calculating plume altitudes. Infrared sounders are essential for detecting ash, as they can distinguishing aerosol type and can be used day and night. While broadband sensors are mainly used for this purpose, they have inherent limitations. Typically, water and ice can mask volcanic ash, while wind blown dust can yield false detection. High spectral resolution sounders should be able to overcome some of these limitations. However, existing detection methods are not easily applicable to hyperspectral sounders and there is therefore a pressing need for novel techniques. In response, we propose a sensitive and robust volcanic ash detection method for hyperspectral sounders based on correlation coefficients and demonstrate it on IASI observations. We show that the method differentiates ash from clouds and dust. Easy to implement, it could contribute to operational volcanic hazard mitigation.


Applied Optics | 2010

Retrieving radius, concentration, optical depth, and mass of different types of aerosols from high-resolution infrared nadir spectra

Lieven Clarisse; Daniel Hurtmans; Alfred J Prata; Federico Karagulian; Cathy Clerbaux; Martine De Mazière; Pierre-François Coheur

We present a sophisticated radiative transfer code for modeling outgoing IR radiation from planetary atmospheres and, conversely, for retrieving atmospheric properties from high-resolution nadir-observed spectra. The forward model is built around a doubling-adding routine and calculates, in a spherical refractive geometry, the outgoing radiation emitted by the Earth and the atmosphere containing one layer of aerosol. The inverse model uses an optimal estimation approach and can simultaneously retrieve atmospheric trace gases, aerosol effective radius, and concentration. It is different from existing codes, as most forward codes dealing with multiple scattering assume a plane-parallel atmosphere, and as for the retrieval, it does not rely on precalculated spectra, the use of microwindows, or two-step retrievals. The simultaneous retrieval on a broad spectral range exploits the full potential of current state-of-the-art hyperspectral IR sounders, such as AIRS and IASI, and should be particularly useful in studying major pollution events. We present five example retrievals of IASI spectra observed in the range from 800 to 1200 cm(-1) above dust, volcanic ash, sulfuric acid, ice particles, and biomass burning aerosols.


Reviews of Geophysics | 2016

Stratospheric Aerosol--Observations, Processes, and Impact on Climate

Stefanie Kremser; Larry W. Thomason; Marc von Hobe; Markus Hermann; Terry Deshler; Claudia Timmreck; Matthew Toohey; Andrea Stenke; Joshua P. Schwarz; R. Weigel; S. Fueglistaler; Fred Prata; Jean-Paul Vernier; Hans Schlager; John E. Barnes; Juan-Carlos Antuña-Marrero; Duncan Fairlie; Mathias Palm; Emmanuel Mahieu; Justus Notholt; Markus Rex; Christine Bingen; Filip Vanhellemont; John M. C. Plane; Daniel Klocke; Simon A. Carn; Lieven Clarisse; Thomas Trickl; Ryan R. Neely; Alexander D. James

Interest in stratospheric aerosol and its role in climate have increased over the last decade due to the observed increase in stratospheric aerosol since 2000 and the potential for changes in the sulfur cycle induced by climate change. This review provides an overview about the advances in stratospheric aerosol research since the last comprehensive assessment of stratospheric aerosol was published in 2006. A crucial development since 2006 is the substantial improvement in the agreement between in situ and space-based inferences of stratospheric aerosol properties during volcanically quiescent periods. Furthermore, new measurement systems and techniques, both in situ and space based, have been developed for measuring physical aerosol properties with greater accuracy and for characterizing aerosol composition. However, these changes induce challenges to constructing a long-term stratospheric aerosol climatology. Currently, changes in stratospheric aerosol levels less than 20% cannot be confidently quantified. The volcanic signals tend to mask any nonvolcanically driven change, making them difficult to understand. While the role of carbonyl sulfide as a substantial and relatively constant source of stratospheric sulfur has been confirmed by new observations and model simulations, large uncertainties remain with respect to the contribution from anthropogenic sulfur dioxide emissions. New evidence has been provided that stratospheric aerosol can also contain small amounts of nonsulfate matter such as black carbon and organics. Chemistry-climate models have substantially increased in quantity and sophistication. In many models the implementation of stratospheric aerosol processes is coupled to radiation and/or stratospheric chemistry modules to account for relevant feedback processes.


IEEE Journal of Selected Topics in Applied Earth Observations and Remote Sensing | 2009

Satellite Monitoring of Volcanic Sulfur Dioxide Emissions for Early Warning of Volcanic Hazards

Meike Rix; Pieter Valks; Nan Hao; J. van Geffen; Cathy Clerbaux; Lieven Clarisse; Pierre-François Coheur; Thilo Erbertseder; Walter Zimmer; Sunil Emmadi

Satellite-based remote sensing measurements of volcanic sulfur dioxide (SO2) provide critical information for reducing volcanic hazards. This paper describes the use of SO2 measurements from the thermal infrared sounder IASI and the UV-VIS instrument GOME-2 in services related to aviation hazard and early warning of volcanic unrest. The high sensitivity of both instruments to SO2 allows the detection and global tracking of volcanic eruption plumes and makes them a valuable tool for volcanic aviation hazard mitigation. The GOME-2 and IASI SO2 data are produced in near-real time and distributed to the Volcanic Ash Advisory Centers (VAACS) to assist them in issuing alerts to airlines and air traffic control organizations. Examples of recent eruptions affecting air traffic are presented including Jebel al Tair (Yemen, September 2007), Mount Okmok (Alaska, July 2008), and Mount Kasatochi (Alaska, August 2008). In addition, GOME-2 can detect changes in the SO2 emissions from passively degassing volcanoes and, therefore, provide critical information for hazard assessment. The monitoring of pre-eruptive degassing by GOME-2 is used in early warning of volcanic activity by a mobile volcano fast response system in combination with numerous other parameters, such as seismicity, deformation, and thermal anomalies.


Geophysical Research Letters | 2014

First simultaneous space measurements of atmospheric pollutants in the boundary layer from IASI: a case study in the North China Plain

Cathy Clerbaux; Lieven Clarisse; Sarah Safieddine; Matthieu Pommier; M. Van Damme; Sophie Bauduin; Charlotte Oudot; Juliette Hadji-Lazaro; Daniel Hurtmans; Pierre-François Coheur

In this paper we investigate a severe pollution episode that occurred in Beijing, Tianjin, and the Hebei province in January 2013. The episode was caused by the combination of anthropogenic emissions and a high-pressure system that trapped pollutants in the boundary layer. Using IASI (Infrared Atmospheric Sounding Interferometer) satellite measurements, high concentrations of key trace gases such as carbon monoxide (CO), sulfur dioxide (SO2), and ammonia (NH3) along with ammonium sulfate aerosol ((NH4)2SO4) are found. We show that IASI is able to detect boundary layer pollution in case of large negative thermal contrast combined with high levels of pollution. Our findings demonstrate that anthropogenic key pollutants, such as CO and SO2, can be monitored by IASI in the North China Plain during wintertime in support of air quality evaluation and management.


Remote Sensing | 2016

Development, Production and Evaluation of Aerosol Climate Data Records from European Satellite Observations (Aerosol_cci)

Thomas Popp; Gerrit de Leeuw; Christine Bingen; C. Brühl; Virginie Capelle; A. Chédin; Lieven Clarisse; Oleg Dubovik; R. G. Grainger; Jan Griesfeller; A. Heckel; Stefan Kinne; Lars Klüser; Miriam Kosmale; Pekka Kolmonen; Luca Lelli; Pavel Litvinov; Linlu Mei; Peter R. J. North; Simon Pinnock; Adam C. Povey; Charles Robert; Michael Schulz; Larisa Sogacheva; Kerstin Stebel; Deborah Stein Zweers; G. E. Thomas; L. G. Tilstra; Sophie Vandenbussche; Pepijn Veefkind

Producing a global and comprehensive description of atmospheric aerosols requires integration of ground-based, airborne, satellite and model datasets. Due to its complexity, aerosol monitoring requires the use of several data records with complementary information content. This paper describes the lessons learned while developing and qualifying algorithms to generate aerosol Climate Data Records (CDR) within the European Space Agency (ESA) Aerosol_cci project. An iterative algorithm development and evaluation cycle involving core users is applied. It begins with the application-specific refinement of user requirements, leading to algorithm development, dataset processing and independent validation followed by user evaluation. This cycle is demonstrated for a CDR of total Aerosol Optical Depth (AOD) from two subsequent dual-view radiometers. Specific aspects of its applicability to other aerosol algorithms are illustrated with four complementary aerosol datasets. An important element in the development of aerosol CDRs is the inclusion of several algorithms evaluating the same data to benefit from various solutions to the ill-determined retrieval problem. The iterative approach has produced a 17-year AOD CDR, a 10-year stratospheric extinction profile CDR and a 35-year Absorbing Aerosol Index record. Further evolution cycles have been initiated for complementary datasets to provide insight into aerosol properties (i.e., dust aerosol, aerosol absorption).


Journal of Geophysical Research | 2014

Separation of ash and sulfur dioxide during the 2011 Grímsvötn eruption

Eldbjørg Dirdal Moxnes; N. I. Kristiansen; Andreas Stohl; Lieven Clarisse; Adam J. Durant; Konradin Weber; Andreas Vogel

Modeling the transport of volcanic ash and gases released during volcanic eruptions is crucially dependent on knowledge of the source term of the eruption, that is, the source strength as a function of altitude and time. For the first time, an inversion method is used to estimate the source terms of both volcanic sulfur dioxide (SO2) and ash. It was applied to the explosive volcanic eruption of Grimsvotn, Iceland, in May 2011. The method uses input from the particle dispersion model, FLEXPART (flexible particle dispersion model), a priori source estimates, and satellite observations of SO2 or ash total columns from Infrared Atmospheric Sounding Interferometer to separately obtain the source terms for volcanic SO2 and fine ash. The estimated source terms show that SO2 was emitted mostly to high altitudes (5 to 13 km) during about 18 h (22 May, 00-18 UTC) while fine ash was emitted mostly to low altitudes (below 4 km) during roughly 24 h (22 May 06 UTC to 23 May 06 UTC). FLEXPART simulations using the estimated source terms show a clear separation of SO2 (transported mostly northwestward) and the fine ash (transported mostly southeastward). This corresponds well with independent satellite observations and measured aerosol mass concentrations and lidar measurements at surface stations in Scandinavia. Aircraft measurements above Iceland and Germany confirmed that the ash was located in the lower atmosphere. This demonstrates that the inversion method, in this case, is able to distinguish between emission heights of SO2 and ash and can capture resulting differences in transport patterns. Key Points Ash and SO2 source terms estimated using inverse techniques and satellite data The transport and separation of ash and SO2 are modeled Model simulations correspond well with a range of independent observations ©2014. The Authors.


Journal of Geophysical Research | 2015

Sulfur dioxide vertical column DOAS retrievals from the Ozone Monitoring Instrument: Global observations and comparison to ground-based and satellite data

Nicolas Theys; I. De Smedt; J. van Gent; Thomas Danckaert; T. Y. Wang; F. Hendrick; Trissevgeni Stavrakou; Sophie Bauduin; Lieven Clarisse; Can Li; N. A. Krotkov; Huan Yu; Hugues Brenot; M. Van Roozendael

We present a new data set of sulfur dioxide (SO2) vertical columns from observations of the Ozone Monitoring Instrument (OMI)/AURA instrument between 2004 and 2013. The retrieval algorithm used is an advanced Differential Optical Absorption Spectroscopy (DOAS) scheme combined with radiative transfer calculation. It is developed in preparation for the operational processing of SO2 data product for the upcoming TROPOspheric Monitoring Instrument/Sentinel 5 Precursor mission. We evaluate the SO2 column results with those inferred from other satellite retrievals such as Infrared Atmospheric Sounding Interferometer and OMI (Linear Fit and Principal Component Analysis algorithms). A general good agreement between the different data sets is found for both volcanic and anthropogenic SO2 emission scenarios. We show that our algorithm produces SO2 columns with low noise and is able to provide accurate estimates of SO2. This conclusion is supported by important validation results over the heavily polluted site of Xianghe (China). Nearly 4 years of OMI and ground-based multiaxis DOAS SO2 columns are compared, and an excellent match is found. We also highlight the improved performance of the algorithm in capturing weak SO2 sources by detecting shipping SO2 emissions in long-term averaged data, an unreported measurement from space.

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Pierre-François Coheur

Université libre de Bruxelles

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Cathy Clerbaux

Université libre de Bruxelles

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Daniel Hurtmans

Université libre de Bruxelles

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Martin Van Damme

Université libre de Bruxelles

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Simon Whitburn

Université libre de Bruxelles

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Nicolas Theys

Belgian Institute for Space Aeronomy

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Ariane Razavi

Université libre de Bruxelles

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Sophie Bauduin

Université libre de Bruxelles

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