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Featured researches published by B. Calpini.


Journal of Geophysical Research | 2007

Validation of Aura Microwave Limb Sounder Ozone by ozonesonde and lidar measurements

Yibo Jiang; L. Froidevaux; Alyn Lambert; Nathaniel J. Livesey; William G. Read; J. W. Waters; Bojan Bojkov; Thierry Leblanc; I. S. McDermid; Sophie Godin-Beekmann; Mark J. Filipiak; R. S. Harwood; R. Fuller; W. H. Daffer; Brian J. Drouin; R. E. Cofield; D. T. Cuddy; R. F. Jarnot; B. W. Knosp; V. S. Perun; Michael J. Schwartz; W. V. Snyder; P. C. Stek; R. P. Thurstans; P. A. Wagner; M. Allaart; S. B. Andersen; G. E. Bodeker; B. Calpini; H. Claude

We present validation studies of MLS version 2.2 upper tropospheric and stratospheric ozone profiles using ozonesonde and lidar data as well as climatological data. Ozone measurements from over 60 ozonesonde stations worldwide and three lidar stations are compared with coincident MLS data. The MLS ozone stratospheric data between 150 and 3 hPa agree well with ozonesonde measurements, within 8% for the global average. MLS values at 215 hPa are biased high compared to ozonesondes by A`20% at middle to high latitude, although there is a lot of variability in this altitude region. Comparisons between MLS and ground-based lidar measurements from Mauna Loa, Hawaii, from the Table Mountain Facility, California, and from the Observatoire de Haute-Provence, France, give very good agreement, within A`5%, for the stratospheric values. The comparisons between MLS and the Table Mountain Facility tropospheric ozone lidar show that MLS data are biased high by A`30% at 215 hPa, consistent with that indicated by the ozonesonde data. We obtain better global average agreement between MLS and ozonesonde partial column values down to 215 hPa, although the average MLS values at low to middle latitudes are higher than the ozonesonde values by up to a few percent. MLS v2.2 ozone data agree better than the MLS v1.5 data with ozonesonde and lidar measurements. MLS tropical data show the wave one longitudinal pattern in the upper troposphere, with similarities to the average distribution from ozonesondes. High upper tropospheric ozone values are also observed by MLS in the tropical Pacific from June to November.


Journal of Geophysical Research | 2007

A trajectory-based estimate of the tropospheric ozone column using the residual method

Mark R. Schoeberl; J. R. Ziemke; B. Bojkov; Nathaniel J. Livesey; B. Duncan; Susan E. Strahan; L. Froidevaux; S. S. Kulawik; Pawan K. Bhartia; S. Chandra; Pieternel F. Levelt; Jacquelyn C. Witte; Anne M. Thompson; E. Cuevas; A. Redondas; David W. Tarasick; J. Davies; G. E. Bodeker; Georg Hansen; Bryan J. Johnson; Samuel J. Oltmans; H. Vömel; M. Allaart; H. Kelder; M. J. Newchurch; Sophie Godin-Beekmann; Gérard Ancellet; H. Claude; S. B. Andersen; E. Kyrö

We estimate the tropospheric column ozone using a forward trajectory model to increase the horizontal resolution of the Aura Microwave Limb Sounder (MLS) derived stratospheric column ozone. Subtracting the MLS stratospheric column from Ozone Monitoring Instrument total column measurements gives the trajectory enhanced tropospheric ozone residual (TTOR). Because of different tropopause definitions, we validate the basic residual technique by computing the 200-hPa-to-surface column and comparing it to the same product from ozonesondes and Tropospheric Emission Spectrometer measurements. Comparisons show good agreement in the tropics and reasonable agreement at middle latitudes, but there is a persistent low bias in the TTOR that may be due to a slight high bias in MLS stratospheric column. With the improved stratospheric column resolution, we note a strong correlation of extratropical tropospheric ozone column anomalies with probable troposphere-stratosphere exchange events or folds. The folds can be identified by their colocation with strong horizontal tropopause gradients. TTOR anomalies due to folds may be mistaken for pollution events since folds often occur in the Atlantic and Pacific pollution corridors. We also compare the 200-hPa-to-surface column with Global Modeling Initiative chemical model estimates of the same quantity. While the tropical comparisons are good, we note that chemical model variations in 200-hPa-to-surface column at middle latitudes are much smaller than seen in the TTOR.


Journal of Geophysical Research | 2012

Southern Hemisphere Additional Ozonesondes (SHADOZ) ozone climatology (2005-2009): Tropospheric and tropical tropopause layer (TTL) profiles with comparisons to OMI-based ozone products

Anne M. Thompson; Sonya K. Miller; Simone Tilmes; Debra W. Kollonige; Jacquelyn C. Witte; Samuel J. Oltmans; Bryan J. Johnson; Masatomo Fujiwara; Francis J. Schmidlin; Gert J. R. Coetzee; Ninong Komala; Matakite Maata; Maznorizan Mohamad; J. Nguyo; C. Mutai; Shin-Ya Ogino; F. Raimundo da Silva; N. M. Paes Leme; Françoise Posny; Rinus Scheele; Henry B. Selkirk; Masato Shiotani; R. Stübi; Gilbert Levrat; B. Calpini; V. Thouret; Haruo Tsuruta; Jessica Valverde Canossa; H. Vömel; Seiichiro Yonemura

[1]xa0We present a regional and seasonal climatology of SHADOZ ozone profiles in the troposphere and tropical tropopause layer (TTL) based on measurements taken during the first five years of Aura, 2005–2009, when new stations joined the network at Hanoi, Vietnam; Hilo, Hawaii; Alajuela/Heredia, Costa Rica; Cotonou, Benin. In all, 15 stations operated during that period. A west-to-east progression of decreasing convective influence and increasing pollution leads to distinct tropospheric ozone profiles in three regions: (1) western Pacific/eastern Indian Ocean; (2) equatorial Americas (San Cristobal, Alajuela, Paramaribo); (3) Atlantic and Africa. Comparisons in total ozone column from soundings, the Ozone Monitoring Instrument (OMI, on Aura, 2004-) satellite and ground-based instrumentation are presented. Most stations show better agreement with OMI than they did for EP/TOMS comparisons (1998–2004; Earth-Probe/Total Ozone Mapping Spectrometer), partly due to a revised above-burst ozone climatology. Possible station biases in the stratospheric segment of the ozone measurement noted in the first 7 years of SHADOZ ozone profiles are re-examined. High stratospheric bias observed during the TOMS period appears to persist at one station. Comparisons of SHADOZ tropospheric ozone and the daily Trajectory-enhanced Tropospheric Ozone Residual (TTOR) product (based on OMI/MLS) show that the satellite-derived column amount averages 25% low. Correlations between TTOR and the SHADOZ sondes are quite good (typical r2= 0.5–0.8), however, which may account for why some published residual-based OMI products capture tropospheric interannual variability fairly realistically. On the other hand, no clear explanations emerge for why TTOR-sonde discrepancies vary over a wide range at most SHADOZ sites.


Journal of Geophysical Research | 2014

Accuracy of ground surface broadband shortwave radiation monitoring

Laurent Vuilleumier; Mathias Hauser; Christian Félix; Franck Vignola; Philippe Blanc; A. Kazantzidis; B. Calpini

The uncertainty of broadband shortwave radiation monitoring is determined for direct, diffuse, and global irradiance for measurements obtained at the Payerne (Switzerland) station of the Baseline Surface Radiation Network (BSRN). The uncertainty estimates include sources that reflect realistic long-term operation conditions. The uncertainties are derived using the methodology specified by the Guide to the expression of uncertainty in measurement. The differences between redundant determinations of direct, diffuse, and global irradiance are analyzed and are shown to be compatible with the uncertainties. In addition, the signatures of some uncertainty sources are sought within the error statistics to find out if corrections can be applied and what their magnitude is. The global and diffuse irradiance uncertainties range from 1.8% to 2.4% without correction and are less than 1.8% with corrections. These uncertainties are close to or satisfy the BSRN targets for large signals (global: 1000 W m A2 , diffuse: 500 W m-2). For small signals (50 W m-2), the targets are not achieved, mainly as a result of uncertainties associated with the data acquisition electronics (DAQ). The direct irradiance uncertainty is ~1.5%, 3 times larger than the BSRN uncertainty target. An accuracy gain can also be achieved at the DAQ level, but even without considering the DAQ uncertainty, the target is exceeded by a factor of about 2. The direct irradiance uncertainty remains ~1% even using an absolute cavity radiometer as transfer standard for correcting the pyrheliometer sensitivity. Thus, the direct irradiance accuracy target of 0.5% is probably not achievable with the best commercially available technology.


Journal of The Electrochemical Society | 1993

Copper Film Growth by Chemical Vapor Deposition Electrical and Optical Measurements in Real Time, and Studies of Morphology

B. Lecohier; B. Calpini; J. M. Philippoz; H. van den Bergh; D. Laub; P. A. Buffat

The deposition of copper by low pressure chem. vapor deposition (CVD) from Cu bis-hexafluoroacetylacetonate is monitored in real time and in situ by the measurement of the optical reflectivity and elec. resistance of the growing metal film. Changes of the deposit morphol. during growth were analyzed by interrupting the CVD process at different stages and observing the samples by transmission electron microscopy. Pure copper is deposited at 400 Deg and 1 mbar total reactor pressure of helium, precursor, and water vapor. Two successive regimes are distinguished in the deposition: island formation and continuous film growth. The transition between these two regimes is visible in the real time specular reflectance measurement. The copper deposition rate is twice higher during the island growth than during the continuous film growth at the applied conditions. The influence of a metal seeding layer (from 0.001 monolayer to 1 monolayer) on the Cu deposition is shown both in the real time measurements and in the ex situ anal. of films.


Atmospheric Environment | 1998

A combined determination of wind velocities and ozone concentrations for a first measurement of ozone fluxes with a DIAL instrument during the MEDCAPHOT-TRACE campaign

Luca Fiorani; B. Calpini; L. Jaquet; H. van den Bergh; Eric Durieux

Abstract From a data set collected during the MEDCAPHOT-TRACE field campaign, we demonstrate that ozone fluxes can be determined with a shot-per-shot DIAL instrument operated in the UV spectral region. This is done by the simultaneous reconstruction of ozone concentrations and of wind speeds using the same sample of lidar returns. A correlation scheme is used for the wind velocity retrieval, in which the transport of the spatial inhomogeneities of the aerosol backscattering coefficient along the optical path of the system is analyzed.


TEMPERATURE: ITS MEASUREMENT AND CONTROL IN SCIENCE AND INDUSTRY, VOLUME 8: Proceedings of the Ninth International Temperature Symposium | 2013

GCOS reference upper air network (GRUAN): Steps towards assuring future climate records

Peter W. Thorne; H. Vömel; G. E. Bodeker; Michael Sommer; A. Apituley; Franz H. Berger; Stephan Bojinski; G. O. Braathen; B. Calpini; Belay Demoz; Howard J. Diamond; J. Dykema; Alessandro Fasso; Masatomo Fujiwara; Tom Gardiner; D. F. Hurst; Thierry Leblanc; Fabio Madonna; A. Merlone; A.C. Mikalsen; C. D. Miller; Tony Reale; K. Rannat; C. Richter; Dian J. Seidel; Masaru Shiotani; D. Sisterson; D.G.H. Tan; Russell S. Vose; J. Voyles

The observational climate record is a cornerstone of our scientific understanding of climate changes and their potential causes. Existing observing networks have been designed largely in support of operational weather forecasting and continue to be run in this mode. Coverage and timeliness are often higher priorities than absolute traceability and accuracy. Changes in instrumentation used in the observing system, as well as in operating procedures, are frequent, rarely adequately documented and their impacts poorly quantified. For monitoring changes in upper-air climate, which is achieved through in-situ soundings and more recently satellites and ground-based remote sensing, the net result has been trend uncertainties as large as, or larger than, the expected emergent signals of climate change. This is more than simply academic with the tropospheric temperature trends issue having been the subject of intense debate, two international assessment reports and several US congressional hearings. For more than a decade the international climate science community has been calling for the instigation of a network of reference quality measurements to reduce uncertainty in our climate monitoring capabilities. This paper provides a brief history of GRUAN developments to date and outlines future plans. Such reference networks can only be achieved and maintained with strong continuing input from the global metrological community.


WIT Transactions on Ecology and the Environment | 1999

Photo-oxidant formation in the Milan metropolitan area

B. Calpini; A. Clappier; R. Jimenez; Gilles Larcheveque; B. Lazzarotto; Alberto Martilli; F. Pasi; Ph Quaglia; V. Simeonov; H. Van den Bergh

During the Limitation of Oxidant Prodn. (LOOP) campaign, different instruments were deployed, providing a complete data set. This will be used to evaluate the model and its ability to reproduce pollution events. Then, the complete data set will be used for a better definition of the model inputs. The final aim of the LOOP project is to use the model to test different abatement strategies, particularly by defining the region where ozone prodn. is NOx or VOC sensitive.


Remote Sensing | 2006

Meteorological water vapor Raman lidar: advances

Todor Dinoev; Pablo Roberto Ristori; Yuri Arshinov; Sergey Bobrovnikov; I. N. Serikov; B. Calpini; H. van den Bergh; V. Simeonov

We present the design and preliminary results of a water vapor Raman lidar, developed explicitly for meteorological applications. The lidar was designed for Meteoswiss as a fully automated, eye-safe instrument for routine water vapor measurements in the troposphere. The lidar is capable of day and nighttime vertical profiling of the tropospheric water vapor with 15 to 30 min temporal resolution. The daytime operation is achieved by decreasing the solar background employing the narrow field-of-view, narrow-band technique. The daytime vertical operational range exceeds 4 km, while the nighttime range is above 7.5 km. The lidar receiver is built on a compact multi-telescope configuration coupled with fibers to a grating polychromator used for spectral separation and partial background suppression. An additional near range fiber in one of the telescopes increases the signal level in the near range and allows water vapor retrieval starting from 100 m. The water vapor mixing ratio is retrieved using the ratio of the water vapor and the nitrogen Raman signals. An additional detection channel for oxygen Raman signal is used for aerosol correction.


WIT Transactions on Ecology and the Environment | 1999

In-situ OH kinetics study providing an indicator for ozone formation limitation

F. Jeanneret; Frank Kirchner; A. Clappier; H. Van den Bergh; B. Calpini

Hydroxyl radicals dominate daytime tropospheric chem., responsible for reactive removal of most trace gases (e.g., volatile org. compds.[VOC]), and is an active participant in the NO and NO2 cycle. Pump-and-probe LIDAR was used to examine the OH- chem. in the planetary boundary layer. This method consists of a high OH- concn. prodn. by a first laser beam (pump), including a flash photolysis of O3: O3 + hv (256 nm) -> O(1D) + O2, and the reaction, O(1D) + H2O -> 2OH. Its relaxation is followed by measuring the time evolution of the radical by laser-induced fluorescence (probe beam). A simulation of this expt. showed that in a short delay time, a direct est. of the total hydrocarbon reactivity defined as SVOC was obtained. The pump-and-probe technique allows measurements which can distinguish between locations where O3 formation mainly depends on NOx concns. and those where it mainly depends on VOC concns.

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V. Simeonov

École Polytechnique Fédérale de Lausanne

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A. Clappier

École Polytechnique Fédérale de Lausanne

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R. Jimenez

École Polytechnique Fédérale de Lausanne

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Frank Kirchner

École Polytechnique Fédérale de Lausanne

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H. van den Bergh

École Polytechnique Fédérale de Lausanne

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