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3. The 2009 edition of the GEISA spectroscopic database

Author

Jacquinet-Husson, N., Crepeau, L., Armante, R., Boutammine, C., Chédin, A., Scott, N.A., Crevoisier, C., Capelle, V., Boone, C., Poulet-Crovisier, N., Barbe, A., Campargue, A., Chris Benner, D., Benilan, Y., Bézard, B., Boudon, V., Brown, L.R., Coudert, L.H., Coustenis, A., Dana, V., Devi, V.M., Fally, S., Fayt, A., Flaud, J.-M., Goldman, A., Herman, M., Harris, G.J., Jacquemart, D., Jolly, A., Kleiner, I., Kleinböhl, A., Kwabia-Tchana, F., Lavrentieva, N., Lacome, N., Xu, Li-Hong, Lyulin, O.M., Mandin, J.-Y., Maki, A., Mikhailenko, S., Miller, C.E., Mishina, T., Moazzen-Ahmadi, N., Müller, H.S.P., Nikitin, A., Orphal, J., Perevalov, V., Perrin, A., Petkie, D.T., Predoi-Cross, A., Rinsland, C.P., Remedios, J.J., Rotger, M., Smith, M.A.H., Sung, K., Tashkun, S., Tennyson, J., Toth, R.A., Vandaele, A.-C., and Vander Auwera, J.

Published
2011
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6. The HITRAN 2008 molecular spectroscopic database

Author

Rothman, L.S., Gordon, I.E., Barbe, A., Benner, D.Chris, Bernath, P.F., Birk, M., Boudon, V., Brown, L.R., Campargue, A., Champion, J.-P., Chance, K., Coudert, L.H., Dana, V., Devi, V.M., Fally, S., Flaud, J.-M., Gamache, R.R., Goldman, A., Jacquemart, D., Kleiner, I., Lacome, N., Lafferty, W.J., Mandin, J.-Y., Massie, S.T., Mikhailenko, S.N., Miller, C.E., Moazzen-Ahmadi, N., Naumenko, O.V., Nikitin, A.V., Orphal, J., Perevalov, V.I., Perrin, A., Predoi-Cross, A., Rinsland, C.P., Rotger, M., Šimečková, M., Smith, M.A.H., Sung, K., Tashkun, S.A., Tennyson, J., Toth, R.A., Vandaele, A.C., and Vander Auwera, J.

Published
2009
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11. Abstracts of the 6th FECS Conference 1998 Lectures

Author

Rowland, F. Sherwood, Blake, Donald R., Larsen, B. R., Lindskog, Anne, Peterson, Peter J., Williams, W. Peter, Wallington, T. J., Pilling, M. J., Carslaw, N., Creasey, D. J., Heard, D. E., Jacobs, P., Lee, J., Lewis, A. C., McQuaid, J. B., Stockwell, William R., Frank, Hartmut, Sacco, P., Cocheo, V., Lynge, E., Andersen, A., Nilsson, R., Barlow, L., Pukkala, E., Nordlinder, R., Boffetta, P., Grandjean, P., Heikkil, P., Hürte, L. G., Jakobsson, R., Lundberg, I., Moen, B., Partanen, T., Riise, T., Borowiak, A., De Saeger, E., Schnitzler, K. G., Gravenhorst, G., Jacobi, H. W., Moelders, S., Lammel, G., Busch, G., Beese, F. O., Dentener, F. J., Feichter, J., Fraedrich, K., Roelofs, G. J., Friedrich, R., Reis, S., Voehringer, F., Simpson, D., Moussiopoulos, N., Sahm, P., Tourlou, P. M., Salmons, R., Papameletiou, D., Maqueda, J. M., Suhr, Per B., Bell, W., Paton-Walsh, C., Woods, P. T., Partridge, R. H., Slemr, J., Slemr, F., Schmidbauer, N., Ravishankara, A. R., Jenkin, Michael E., de Leeuw, G., van Eijk, A. M. J., Flossmann, A. I., Wobrock, W., Mestayer, P. G., Tranchant, B., Ljungström, E., Karlsson, R., Larsen, S. E., Roemer, M., Builtjes, P. J. H., Koffi, Brigitte, Koffi, Ernest N’Dri, De Saeger, Emile, Ro-Poulsen, H., Mikkelsen, T. N., Hummelshøj, P., Hovmand, M. F., Simoneit, Bernd R. T., van der Meulen, A., Meyer, Michael B., Berndt, T., Böge, O., Stratmann, F., Cass, Glen R., Harrison, Roy M., Shi, Ji Ping, Hoffmann, T., Warscheid, B., Bandur, R., Marggraf, U., Nigge, W., Kamens, Richard, Jang, Myoseon, Strommen, Mike, Chien, Chao-Jung, Leach, Keri, Ammann, M., Kalberer, M., Arens, F., Lavanchy, V., Gâggeler, H. W., Baltensperger, U., Davies, J. A., Cox, R. A., Alonso, S. García, Pastor, R. Pérez, Argüello, Gustavo A., Willner, Helge, Berndt, T., Böge, O., Bogillo, V. I., Pokrovskiy, V. A., Kuraev, O. V., Gozhyk, P. F., Bolzacchini, E., Bruschi, M., Fantucci, P., Meinardi, S., Orlandi, M., Rindone, B., Bolzacchini, Ezio, Bohn, Birger, Rindone, Bruno, Bruschi, Maurizo, Zetzsch, Cornelius, Brussol, C., Duane, M., Larsen, B., Carlier, P., Kotzias, D., Caracena, A. Baeza, Aznar, A. Miñana, Ferradás, E. González, Christensen, C. S., Skov, H., Hummelshøj, P., Jensen, N. O., Lohse, C., Cocheo, V., Sacco, P., Chatzis, C., Cocheo, V., Sacco, P., Boaretto, C., Quaglio, F., Zaratin, L., Pagani, D., Cocheo, L., Cocheo, Vincenzo, Asnar, Agustin Minana, Baldan, Annerita, Ballesta, Pascual P., Boaretto, Caterina, Caracena, Antonia B., Ferradas, Enrique Gonzalez, Gonzalez-Flesca, Nobert, Goelen, Eddie, Hansen, Asger B., Sacco, Paolo, De Saeger, Emile, Skov, Henrik, Consonni, V., Gramatica, P., Santagostino, A., Galvani, P., Bolzacchini, E., Consonni, Viviana, Gramatica, Paola, Todeschini, Roberto, Dippel, G., Reinhardt, H., Zellner, R., Dämmer, K., Bednarek, G., Breil, M., Zellner, R., Febo, A., Allegrini, I., Giliberti, C., Perrino, C., Fogg, P. G. T., Geiger, H., Barnes, I., Becker, K. H., Maurer, T., Geyskens, F., Bormans, R., Lambrechts, M., Goelen, E., Giese, Martina, Frank, Hartmut, Glasius, M., Hornung, P., Jacobsen, J. K., Klausen, H. S., Klitgaard, K. C., Møller, C. K., Petersen, A. P. F., Petersen, L. S., Wessel, S., Hansen, T. S., Lohse, C., Boaretto, E., Heinemeier, J., Glasius, M., Di Bella, D., Lahaniati, M., Calogirou, A., Jensen, N. R., Hjorth, J., Kotzias, D., Larsen, B. R., Gonzalez-Flesca, N., Cicolella, A., Bates, M., Bastin, E., Gurbanov, M. A., Akhmedly, K. M., Balayev, V. S., Haselmann, K. F., Ketola, R., Laturnus, F., Lauritsen, F. R., Grøn, C., Herrmann, H., Ervens, B., Reese, A., Umschlag, Th., Wicktor, F., Zellner, R., Herrmann, H., Umschlag, Th., Müller, K., Bolzacchini, E., Meinardi, S., Rindone, B., Jenkin, Michael E., Hayman, Garry D., Jensen, N. O., Courtney, M., Hummelshøj, P., Christensen, C. S., Larsen, B. R., Johnson, Matthew S., Hegelund, Flemming, Nelander, Bengt, Kirchner, Frank, Klotz, B., Barnes, Ian, Sørensen, S., Becker, K. H., Etzkorn, T., Platt, U., Wirtz, K., Martín-Reviejo, M., Laturnus, Frank, Martinez, E., Cabañas, B., Aranda, A., Martín, P., Salgado, S., Rodriguez, D., Masclet, P., Jaffrezo, J. L., Hillamo, R., Mellouki, A., Le Calvé, S., Le Bras, G., Moriarty, J., O’Donnell, S., Wenger, J., Sidebottom, H., Mingarrol, M. T. Bomboi, Cosin, S., Pastor, R. Pérez, Alonso, S. García, Sanz, M. J., Bravo, I., Gonzalez, D., Pérez, M. A., Mustafaev, Islam, Mammadova, Saida, Noda, J., Hallquist, M., Langer, S., Ljungström, E., Nohara, K., Kutsuna, S., Ibusuki, T., Oehme, Michael, Kölliker, Stephan, Brombacher, Stephan, Merz, Leo, Pastor, R. Pérez, Alonso, S. García, Cabezas, A. Quejido, Peeters, J., Vereecken, L., El Yazal, J., Pfeffer, Hans-Ulrich, Breuer, Ludger, Platz, J., Nielsen, O. J., Sehested, J., Wallington, T. J., Ball, J. C., Hurley, M. D., Straccia, A. M., Schneider, W. F., Pérez-Casany, M. P., Nebot-Gil, I., Sánchez-Marín, J., Putz, E., Folberth, G., Pfister, G., Weissflog, L., Elansky, N. P., Sørensen, Søren, Barnes, Ian, Becker, K. H., Shao, M., Heiden, A. C., Kley, D., Rockel, P., Wildt, J., Silva, G. V. A., Vasconcelos, M. T., Fernandes, E. O., Santos, A. M. S., Skov, Henrik, Hansen, Asger, Løfstrøm, Per, Lorenzen, Gitte, Stabel, J. R., Wolkoff, P., Pedersen, T., Strom, A. B., Skov, Henrik, Hertel, Ole, Jensen, Finn Palmgren, Hjorth, Jens, Galle, Bosse, Wallin, Svante, Theloke, J., Libuda, H. G., Zabel, F., Touaty, Muriel, Bonsang, Bernard, Ullerstam, M., Langer, S., Ljungström, E., Wenger, John, Bonard, Amélie, Manning, Marcus, Nolan, Sinéad, O’Sullivan, Niamh, Sidebottom, Howard, Wenger, John, Collins, Eoin, Moriarty, Jennie, O’Donnell, Sinéad, Sidebottom, Howard, Wenger, John, Collins, Eoin, Moriarty, Jennie, O’Donnell, Sinéad, Sidebottom, Howard, Wenger, John, Sidebottom, Howard, Chadwick, Paul, O’Leary, Barbara, Treacy, Jack, Wolkoff, Peder, Clausen, Per A., Wilkins, Cornelius K., Hougaard, Karin S., Nielsen, Gunnar D., Zilinskis, Viktors, Jansons, Guntis, Peksens, Aigars, Lazdins, Agris, Arinci, Y. V., Erdöl, N., Ekinci, E., Okutan, H., Manlafalioglu, I., Bakeas, Evangelos B., Siskos, Panayotis A., Viras, Loizos G., Smirnioudi, Vasiliki N., Bottenheim, Jan W., Biesenthal, Thomas, Gong, Wanmin, Makar, Paul, Delmas, Véronique, Menard, Tamara, Tatry, Véronique, Moussafir, Jacques, Thomas, Dominique, Coppalle, Alexis, Ellermann, Thomas, Hertel, Ole, Skov, Henrik, Frohn, Lise, Manscher, Ole H., Friis, Jørgen, Girgzdiene, Rasa, Girgzdys, Aloyzas, Gurevich, N. A., Gårdfeldt, Katarina, Langer, Sarka, Hermans, C., Vandaele, A. C., Carleer, M., Fally, S., Colin, R., Bernath, P. F., Jenouvrier, A., Coquart, B., Mérienne, M. -F., Hertel, Ole, Frohn, Lise, Skov, Henrik, Ellermann, Thomas, Huntrieser, H., Schlager, H., Feigl, C., Kemp, Kåre, Palmgren, Finn, Kiilsholm, Sissi, Rasmussen, Alix, Sørensen, Jens Havskov, Klemm, Otto, Lange, Holger, Larsen, René Wugt, Larsen, Niels Wessel, Nicolaisen, Flemming, Sørensen, Georg Ole, Beukes, Jon Are, Larsen, Poul Bo, Jensen, Steen Solvang, Fenger, Jes, de Leeuw, Gerrit, Kunz, Gerard, Cohen, Leo, Schlünzen, Heinke, Muller, Frank, Schulz, Michael, Tamm, Susanne, Geernaert, Gary, Hertel, Ole, Pedersen, Britta, Geernaert, Lise Lotte Sørensen, Lund, Søren, Vignati, Elisabetta, Jickells, Tim, Spokes, Lucinda, Matei, C., Jinga, O. A., Jinga, D. C., Moliner, R., Braekman-Danheux, C., Fontana, A., Suelves, I., Thieman, T., Vassilev, S., Skov, Henrik, Hertel, Ole, Zlatev, Zahari, Brandt, Jørgen, Bastrup-Birk, Annemarie, Ellermann, Thomas, Frohn, Lise, Vandaele, A. C., Hermans, C., Carleer, M., Tsouli, A., Colin, R., Windsperger, Andreas M., Turi, Kristina, Dworak, Oliver, Zellweger, C., Weingartner, E., Rüttimann, R., Hofer, P., Baltensperger, U., Ziv, A., Iakovleva, E., Palmgren, F., Berkovicz, R., Skov, H., Alastuey, A., Querol, X., Chaves, A., Lopez-Soler, A., Ruiz, C., Andrees, J. M., Allegrini, I., Febo, A., Giusto, M., Angeloni, M., Di Filippo, P., D’Innocenzio, F., Lepore, L., Marconi, A., Arshinov, M. Yu., Belan, B. D., Davydov, D. K., Kovaleskii, V. K., Plotinov, A. P., Pokrovskii, E. V., Sklyadneva, T. K., Tolmachev, G. N., Arshinov, M. Yu., Belan, B. D., Sklyadneva, T. K., Behnke, Wolfgang, Elend, Manfred, Krüger, Ulrich, Zetzsch, Cornelius, Belan, B. D., Arshinov, M. Yu., Davydov, D. K., Kovalevskii, V. K., Plotnikov, A. P., Pokrovskii, E. V., Rasskazchikova, T. M., Sklyadneva, T. K., Tolmachev, G. N., Belan, B. D., Arshinov, M. Yu., Simonenkov, D. V., Tolmachev, G. N., Bilde, Merete, Aker, Pamela M., Börensen, C., Kirchner, U., Scheer, V., Vogt, R., Ellermann, T., Geernaert, L. L. S., Pryor, S. C., Barthelmie, R. J., Feilberg, Anders, Nielsen, Torben, Kamens, Richard M., Freitas, M. C., Marques, A. P., Reis, M. A., Alves, L. C., Ilyinskikh, N. N., Ilyinskikh, I. N., Ilyinskikh, E. N., Johansen, Keld, Stavnsbjerg, Peter, Gabrielsson, Pär, Bak, Flemming, Andersen, Erik, Autrup, Herman, Kamens, Richard, Jang, Myoseon, Strommen, Michael, Leach, Keri, Kirchner, U., Scheer, V., Börensen, C., Vogt, R., Igor, Komov, Svjatoslav, Galiy, Anatoliy, Burlak, Komov, I. L., Istchenko, A. A., Lourenço, M. G., MacTavish, D., Sirois, A., Masclet, Pierre, Jaffrezo, Jean Luc, van der Meulen, A., Milukaite, A., Morkunas, V., Jurgutis, P., Mikelinskiene, A., Nielsen, Torben, Feilberg, Anders, Binderup, Mona Lise, Pineda, M., Palacios, J. M., Garcia, E., Cilleruelo, C., Moliner, R., Popovitcheva, O. B., Trukhin, M. E., Persiantseva, N. M., Buriko, Yu, Starik, A. M., Demirdjian, B., Suzanne, J., Probst, T. U., Rietz, B., Alfassi, Z. B., Pokrovskiy, V. A., Zenobi, R., Bogatyr’ov, V. M., Gun’ko, V. M., Querol, X., Alastuey, A., Lopez-Soler, A., Mantilla, E., Plana, F., Artiño, B., Rauterberg-Wulff, A., Israël, G. W., Rocha, Teresa A. P., Duarte, Armando C., Röhrl, Andreas, Lammel, Gerhard, Spindler, G., Müller, K., Herrmann, H., Strommen, Michael R., Vignati, Elisabetta, de Leeuw, Gerrit, and Berkowicz, Ruwim

Published
1998
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14. Improved water vapour spectroscopy in the 4174-4300 cm⁻¹ region and its impact on SCIAMACHY HDO/H₂O measurements

Author

Scheepmaker, R. A., Frankenberg, C., Galli, A., Butz, A., Schrijver, H., Deutscher, N. M., Wunch, D., Warneke, T., Fally, S., and Aben, I.

Subjects
Earth sciences, ddc:550
Abstract

The relative abundance of the heavy water isotopologue HDO provides a deeper insight into the atmospheric hydrological cycle. The SCanning Imaging Absorption spectroMeter for Atmospheric CartograpHY (SCIAMACHY) allows for global retrievals of the ratio HDO/HO in the 2.3 micron wavelength range. However, the spectroscopy of water lines in this region remains a large source of uncertainty for these retrievals. We therefore evaluate and improve the water spectroscopy in the range 4174–4300 cm⁻¹ and test if this reduces systematic uncertainties in the SCIAMACHY retrievals of HDO/H₂O. We use a laboratory spectrum of water vapour to fit line intensity, air broadening and wavelength shift parameters. The improved spectroscopy is tested on a series of ground-based high resolution FTS spectra as well as on SCIAMACHY retrievals of H2O and the ratio HDO/H₂O. We find that the improved spectroscopy leads to lower residuals in the FTS spectra compared to HITRAN 2008 and Jenouvrier et al. (2007) spectroscopy, and the retrievals become more robust against changes in the retrieval window. For both the FTS and SCIAMACHY measurements, the retrieved total H₂O columns decrease by 2–4% and we find a negative shift of the HDO/H₂O ratio, which for SCIAMACHY is partly compensated by changes in the retrieval setup and calibration software. The updated SCIAMACHY HDO/H₂O product shows somewhat steeper latitudinal and temporal gradients and a steeper Rayleigh distillation curve, strengthening previous conclusions that current isotope-enabled general circulation models underestimate the variability in the near-surface HDO/H₂O ratio.

Published
2013

15. IUPAC critical evaluation of the rotational-vibrational spectra of water vapor. Part II: Energy levels and transition wavenumbers for HD16O, HD17O, and HD18O

Author

Tennyson, Jonathan, Bernath, P. F., Brown, Linda, Campargue, Alain, Csaszar, Attila G, Daumont, L., Gamache, Robert, Hodges, J.T., Naumenko, O. V., Polyansky, O., Rothman, L. S., Toth, R.-A., Vandaele, Ann Carine, Zobov, N.F., Fally, S., Fazliev, A. Z., Furtenbacher, T., Gordon, I.E., Hu, Shui-Ming, Mikhailenko, S. N., Voronin, Boris A, Department of Physics and Astronomy [UCL London], University College of London [London] ( UCL ), Jet Propulsion Laboratory ( JPL ), California Institute of Technology ( CALTECH ) -NASA, LIPhy-LAME, Laboratoire Interdisciplinaire de Physique [Saint Martin d’Hères] ( LIPhy ), Université Joseph Fourier - Grenoble 1 ( UJF ) -Centre National de la Recherche Scientifique ( CNRS ) -Université Joseph Fourier - Grenoble 1 ( UJF ) -Centre National de la Recherche Scientifique ( CNRS ), Department of Environmental, Earth, and Atmospheric Sciences [Lowell], University of Massachusetts at Lowell ( UMass Lowell ), Open Laboratory of Bond Selective Chemistry, University of Science and Technology of China [Hefei] ( USTC ), Department of Chemistry [Waterloo], University of Waterloo [Waterloo], Department of Chemistry [York, UK], University of York [York, UK], Laboratoire de Spectrométrie Physique ( LSP ), Université Joseph Fourier - Grenoble 1 ( UJF ) -Centre National de la Recherche Scientifique ( CNRS ), Laboratory of Molecular Spectroscopy, Institute of Chemistry, Groupe de spectrométrie moléculaire et atmosphérique - UMR 7331 ( GSMA ), Université de Reims Champagne-Ardenne ( URCA ) -Centre National de la Recherche Scientifique ( CNRS ), Physics Laboratory ( NIST ), National Institute of Standards and Technology [Gaithersburg] ( NIST ), Institute of Atmospheric Optics ( IAO ), Siberian Branch of the Russian Academy of Sciences ( SB RAS ), Institute of Applied Physics of RAS, Russian Academy of Sciences [Moscow] ( RAS ), Atomic and Molecular Physics Division ( AMPD ), Harvard-Smithsonian Center for Astrophysics, Belgian Institute for Space Aeronomy / Institut d'Aéronomie Spatiale de Belgique ( BIRA-IASB ), Institut of Applied Physics ( IAP ), Service de Chimie Quantique et Photophysique, Université Libre de Bruxelles [Bruxelles] ( ULB ), Institute of Atmospheric Optics SB RAS, Eötvös Loránd University ( ELTE ), V.E. Zuev Institute of Atmospheric Optics ( IAO ), University College of London [London] (UCL), Jet Propulsion Laboratory (JPL), NASA-California Institute of Technology (CALTECH), LAsers, Molécules et Environnement (LAME-LIPhy), Laboratoire Interdisciplinaire de Physique [Saint Martin d’Hères] (LIPhy), Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF)-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF), University of Massachusetts [Lowell] (UMass Lowell), University of Massachusetts System (UMASS)-University of Massachusetts System (UMASS), University of Science and Technology of China [Hefei] (USTC), Laboratoire de Spectrométrie Physique (LSP), Université Joseph Fourier - Grenoble 1 (UJF)-Centre National de la Recherche Scientifique (CNRS), Groupe de spectrométrie moléculaire et atmosphérique (GSMA), Université de Reims Champagne-Ardenne (URCA)-Centre National de la Recherche Scientifique (CNRS), Physics Laboratory (NIST), National Institute of Standards and Technology [Gaithersburg] (NIST), V.E. Zuev Institute of Atmospheric Optics (IAO), Siberian Branch of the Russian Academy of Sciences (SB RAS), Russian Academy of Sciences [Moscow] (RAS), Atomic and Molecular Physics Division [Cambridge] (AMP), Harvard-Smithsonian Center for Astrophysics (CfA), Harvard University [Cambridge]-Smithsonian Institution-Harvard University [Cambridge]-Smithsonian Institution, Belgian Institute for Space Aeronomy / Institut d'Aéronomie Spatiale de Belgique (BIRA-IASB), Institut of Applied Physics (IAP), Université libre de Bruxelles (ULB), and Eötvös Loránd University (ELTE)

Subjects
HD17O, [PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics], HD16O, Aéronomie, [ PHYS.PHYS.PHYS-OPTICS ] Physics [physics]/Physics [physics]/Optics [physics.optics], [PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph], [ PHYS.PHYS.PHYS-ATOM-PH ] Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph], Atmospheric physics, HD18O, Infrared spectra, W@DIS, Information system, Database, Microwave spectra, Spectroscopie [électromagnétisme, optique, acoustique], Transition wavenumbers, Chimie quantique, Energy levels, MARVEL, ComputingMilieux_MISCELLANEOUS, Water vapor
Abstract

This is the second of a series of articles reporting critically evaluated rotational-vibrational line positions, transition intensities, pressure dependences, and energy levels, with associated critically reviewed assignments and uncertainties, for all the main isotopologues of water. This article presents energy levels and line positions of the following singly deuterated isotopologues of water: HD16O, HD17O, and HD18O. The MARVEL (measured active rotational-vibrational energy levels) procedure is used to determine the levels, the lines, and their self-consistent uncertainties for the spectral regions 0-22708, 0-1674, and 0-12105cm-1 for HD16O, HD17O, and HD18O, respectively. For HD16O, 54740 transitions were analyzed from 76 sources, the lines come from spectra recorded both at room temperature and from hot samples. These lines correspond to 36690 distinct assignments and 8818 energy levels. For HD17O, only 485 transitions could be analyzed from three sources; the lines correspond to 162 MARVEL energy levels. For HD18O, 8729 transitions were analyzed from 11 sources and these lines correspond to 1864 energy levels. The energy levels are checked against ones determined from accurate variational nuclear motion computations employing exact kinetic energy operators. This comparison shows that the measured transitions account for about 86% of the anticipated absorbance of HD16O at 296K and that the transitions predicted by the MARVEL energy levels account for essentially all the remaining absorbance. The extensive list of MARVEL lines and levels obtained are given in the Supplementary Material of this article, as well as in a distributed information system applied to water, W@DIS, where they can easily be retrieved. In addition, the transition and energy level information for H217O and H218O, given in the first paper of this series [Tennyson, et al. J Quant Spectr Rad Transfer 2009;110:573-96], has been updated. © 2010 Elsevier Ltd., SCOPUS: ar.j, info:eu-repo/semantics/published

Published
2010
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16. HDO and D2O long path spectroscopy: Ongoing work of the Brussels-Reims Team

Author

Daumont, Ludovic, Jenouvrier, A., Carleer, M., Fally, S., Vandaele, A. C., and Hermans, C.

Subjects
HITRAN, Astronomical spectroscopy
Abstract

Laboratory absorption spectra of H2O-D2O mixtures have been recorded in the spectral region 8800-1500 cm-1 by Fourier transform spectroscopy at high resolution (0.03 cm-1 ). The 50 m base long cell from Reims was used to record spectra with total pressure £ absorption path products of about 6000 torr m. In the continuation of our previous work concerning water vapor 1 ; 2 ; 3 ; 4 ; 5 ; 6 ; 7 ; 8 ; 9 ; 10 , the present study deals with the Deuterium enriched spectra. Two spectra with diÆerent mixing ratios for H 2 O, HDO and D 2 O species were recorded. The identiØcation of the HDO and D 2 O lines has been made by comparison of ratios between pure and enriched spectra. Partial pressures were carefully determined using (i) H2 ^16O previously determined line intensities, (ii) HDO and D 2 O line intensity ratios, and (iii) total pressures. The lines identiØcation was checked through the evolution of the integrated absorption coe±cients with the partial pressures. The observed lines have been Øtted to Voigt line proØles from which line positions (cali- brated afterwards), integrated absorption cross-sections and self-broadening coe±cients have been determined. For the two deuterated species the integrated absorption cross sections could be measured down to 5 10-27 cm/molecule. Comparisons with the most recent experimental data and calculations are presented.

Published
2006
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17. Water vapour line assignments in the 9250-26 000 cm (-1) frequency range

Author

Tolchenov, R. N., Naumenko, O., Zobov, N. F., Shirin, S. V., Polyansky, O. L., Tennyson, J., Carleer, M., Coheur, P. F., Fally, S., Jenouvrier, A., and Vandaele, A. C.

Subjects
water vapour, line assignments, atmospheric radiation, HIGH-RESOLUTION SPECTRUM, POTENTIAL-ENERGY SURFACE, ABSORPTION-SPECTRUM, CM(-1) REGION, MU-M, ROVIBRATIONAL ANALYSIS, ICLAS-VECSEL, CAVITY-RING, POSITIONS, PARAMETERS
Abstract

Line parameters for water vapour in natural abundance have recently been determined for the 9250-13 000 cm(-1) region [M.-F. Wrienne, A. Jenouvrier, C. Hermans, A.C. Vandaele, M. Carleer, C. Clerbaux, P.-F. Coheur, R. Colin, S. Fally, M. Bach, J. Quant. Spectrosc. Radiat. Transfer 82 (2003) 99] and the 13 000-26 000 cm(-1) region [P.-F. Coheur, S. Fally, M. Carleer, C. Clerbaux, R. Colin, A. Jenouvrier, M.-F. Wrienne, C. Hermans, A.C. Vandaele, J. Quant. Spectrosc. Radial. Transfer 74 (2002) 493] using a high-resolution Fourier-transform spectrometer with a long-path absorption cell. These spectra are analysed using several techniques including variational line lists and assignments made. In total, over 15 000 lines were assigned to transitions involving more than 150 exited vibrational states of (H2O)-O-16. Twelve new vibrational band origins are determined and estimates for a further 16 are presented. (c) 2005 Elsevier Inc. All rights reserved.

Published
2005

18. Improved water vapour spectroscopy in the 4174-4300 cm(-1) region and its impact on SCIAMACHY HDO/H2O measurements

Author

Scheepmaker, R A, Frankenberg, C, Galli, A, Butz, A, Schrijver, H, Deutscher, N M, Wunch, D, Warneke, T, Fally, S, Aben, I, Scheepmaker, R A, Frankenberg, C, Galli, A, Butz, A, Schrijver, H, Deutscher, N M, Wunch, D, Warneke, T, Fally, S, and Aben, I

Abstract

The relative abundance of the heavy water isotopologue HDO provides a deeper insight into the atmospheric hydrological cycle. The SCanning Imaging Absorption spectroMeter for Atmospheric CartograpHY (SCIAMACHY) allows for global retrievals of the ratio HDO/H2O in the 2.3 micron wavelength range. However, the spectroscopy of water lines in this region remains a large source of uncertainty for these retrievals. We therefore evaluate and improve the water spectroscopy in the range 4174-4300 cm(-1) and test if this reduces systematic uncertainties in the SCIAMACHY retrievals of HDO/H2O. We use a laboratory spectrum of water vapour to fit line intensity, air broadening and wavelength shift parameters. The improved spectroscopy is tested on a series of ground-based high resolution FTS spectra as well as on SCIAMACHY retrievals of H2O and the ratio HDO/H2O. We find that the improved spectroscopy leads to lower residuals in the FTS spectra compared to HITRAN 2008 and Jenouvrier et al. (2007) spectroscopy, and the retrievals become more robust against changes in the retrieval window. For both the FTS and SCIAMACHY measurements, the retrieved total H2O columns decrease by 2-4% and we find a negative shift of the HDO/H2O ratio, which for SCIAMACHY is partly compensated by changes in the retrieval setup and calibration software. The updated SCIAMACHY HDO/H2O product shows somewhat steeper latitudinal and temporal gradients and a steeper Rayleigh distillation curve, strengthening previous conclusions that current isotope-enabled general circulation models underestimate the variability in the near-surface HDO/H2O ratio.

Published
2013

22. Ground-based FTIR and MAX-DOAS observations of formaldehyde at Réunion Island and comparisons with satellite and model data

Author

Vigouroux, C., primary, Hendrick, F., additional, Stavrakou, T., additional, Dils, B., additional, De Smedt, I., additional, Hermans, C., additional, Merlaud, A., additional, Scolas, F., additional, Senten, C., additional, Vanhaelewyn, G., additional, Fally, S., additional, Carleer, M., additional, Metzger, J.-M., additional, Müller, J.-F., additional, Van Roozendael, M., additional, and De Mazière, M., additional

Published
2009
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25. Technical Note: New ground-based FTIR measurements at Ile de La Réunion: observations, error analysis, and comparisons with independent data

Author

Senten, C., primary, De Mazière, M., additional, Dils, B., additional, Hermans, C., additional, Kruglanski, M., additional, Neefs, E., additional, Scolas, F., additional, Vandaele, A. C., additional, Vanhaelewyn, G., additional, Vigouroux, C., additional, Carleer, M., additional, Coheur, P. F., additional, Fally, S., additional, Barret, B., additional, Baray, J. L., additional, Delmas, R., additional, Leveau, J., additional, Metzger, J. M., additional, Mahieu, E., additional, Boone, C., additional, Walker, K. A., additional, Bernath, P. F., additional, and Strong, K., additional

Published
2008
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32. Improved water vapour spectroscopy in the 4174-4300cm-1 region and its impact on SCIAMACHY HDO/H2O measurements.

Author

Scheepmaker, R. A., Frankenberg, C., Galli, A., Butz, A., Schrijver, H., Deutscher, N. M., Wunch, D., Warneke, T., Fally, S., and Aben, I.

Subjects
SPECTRUM analysis, ATMOSPHERIC water vapor, DEUTERIUM oxide, ABSORPTION spectra, CARTOGRAPHY, FOURIER transform spectroscopy
Abstract

The article focuses on a study on water vapour spectroscopy and its impact on the ratio of heavy water (HDO) and water (H2O) in Scanning Imaging Absorption spectrometer for Atmospheric Cartography (SCIAMACHY). In the study,the impact of updated water spectroscopy is tested on total column retrievals of high-resolution Fourier-Transform Spectrometers (FTS). It shows negative shift in the HDO/H2O ratio for both the SCHIAMACHY and FTS measurements.

Published
2012
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34. Fourier Transform Spectroscopy of the O2Herzberg Bands. III. Absorption Cross Sections of the Collision-Induced Bands and of the Herzberg Continuum

Author

Fally, S., Vandaele, A.C., Carleer, M., Hermans, C., Jenouvrier, A., Mérienne, M.-F., Coquart, B., and Colin, R.

Abstract

Absorption spectra of molecular oxygen were measured in the laboratory under temperature and pressure conditions prevailing in the Earth's atmosphere. Spectra of pure O2, O2+ N2, and O2+ Ar were recorded in the 41 700 to 33 000 cm−1region (240–300 nm) at a maximal optical path difference of 0.45 cm using a Fourier transform spectrometer and a multiple reflection gas cell. The different components of the spectra, namely the discrete bands of the three Herzberg systems, the Herzberg continuum, and the collision-induced diffuse Wulf bands, were separated. The contribution of the Herzberg bands was first subtracted using the line parameters determined previously [A. Jenouvrier, M.-F. Mérienne, B. Coquart, M. Carleer, S. Fally, A. C. Vandaele, C. Hermans, and R. Colin, J. Mol. Spectrosc.198, 136–162 (1999)] from high-resolution data. Spectra recorded at various pressures then made it possible to determine by linear regression the intensity of the Wulf bands and the Herzberg continuum. The characteristics of the Wulf bands have been investigated in details: vibrational analysis, pressure effect, foreign gas effect, and a simulated spectrum are reported. The Herzberg continuum cross section is determined below the dissociation limit. A comparison with literature data is given. The new O2absorption cross sections and O2–O2collision-induced absorption cross sections are useful in connection with atmospheric measurements of ozone and other trace gases in the UV spectral region.

Published
2000
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35. Fourier Transform Spectroscopy of the O2Herzberg Bands

Author

Mérienne, M.-F., Jenouvrier, A., Coquart, B., Carleer, M., Fally, S., Colin, R., Vandaele, A.C., and Hermans, C.

Abstract

From absorption spectra obtained at high resolution by coupling a Fourier transform spectrometer to a long-path multiple reflection cell [A. Jenouvrier, M.-F. Mérienne, B. Coquart, M. Carleer, S. Fally, A. C. Vandaele, C. Hermans, and R. Colin, J. Mol. Spectrosc.198, 136–162 (1999)] the intensities of the O2Herzberg bands (A3Σ+u–X3Σ−g, c1Σ−u–X3Σ−g, A′3Δu–X3Σ−g) have been studied at ambient temperature. The integrated cross section values are given for the lines of the (v′–0) bands in the A3Σ+u–X3Σ−g, c1Σ−u–X3Σ−g, and A′3Δu–X3Σ−gtransitions with v′ = 0–11, v′ = 2–19, and v′ = 2–12, respectively. The band oscillator strengths have been deduced and transition moments have been calculated. The total absorption values in the region of the Herzberg bands together with the photoabsorption values determined previously above the dissociation limit can be modeled by a single curve, in agreement with the continuity relationship of the cross sections through the dissociation limit.

Published
2000
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40. Fourier transform measurements of SO2 absorption cross sections: II.: Temperature dependence in the 29000–44000cm−1 (227–345nm) region

Author

Vandaele, A.C., Hermans, C., and Fally, S.

Subjects
*FOURIER transforms, *SULFUR dioxide, *ABSORPTION, *TEMPERATURE effect, *ULTRAVIOLET radiation, *PLANETARY spectra
Abstract

Abstract: This paper is the second of a series that reports results on the measurements of the absorption cross section of SO2 in the UV/visible region at high resolution and that investigates high temperatures in support to planetary applications. Absorption cross sections of SO2 have been obtained in the 29000–44000cm−1 spectral range (227–345nm) with a Fourier transform spectrometer at a resolution of 2cm−1 (0.4500cm MOPD and boxcar apodisation). Pure SO2 samples were used and measurements were performed at room temperature (298K) as well as at 318, 338 and 358K. Temperature effects in this spectral region are investigated and are favorably compared to existing studies in the literature. Comparison of the absorption cross section at room temperature shows good agreement in intensity with most of the literature data, but shows that most of the latter suffer from inaccurate wavelength scale definition. Moreover, literature data are often given only on restricted spectral intervals. Combined with the data described in the first part of this series of papers on SO2, this new data set offers the considerable advantage of covering the large spectral interval extending from 24000 to 44000cm−1 (227–420nm), at the four temperatures investigated. [Copyright &y& Elsevier]

Published
2009
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41. Fourier transform measurements of SO2 absorption cross sections:: I. Temperature dependence in the 24000–29000cm−1 (345–420nm) region

Author

Hermans, C., Vandaele, A.C., and Fally, S.

Subjects
*FOURIER transform spectroscopy, *ABSORPTION cross sections, *SULFUR dioxide, *TEMPERATURE effect, *SPECTRUM analysis
Abstract

Abstract: Absorption cross sections of SO2 have been obtained in the 24000–29000cm−1 spectral range (345–420nm) with a Fourier transform spectrometer at a resolution of 2cm−1. Pure SO2 samples were used and measurements were performed at room temperature (298K) as well as at 318, 338 and 358K. This is the first time that temperature effects in this spectral region are reported and investigated. This paper is the first of a series that will report on measurements of the absorption cross section of SO2 in the UV/visible region at a higher than previously reported resolution and that will investigate temperature effects in support of tropospheric, stratospheric and astrophysical or planetary applications. [Copyright &y& Elsevier]

Published
2009
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42. Absorption cross-sections of <f>NO2</f>: simulation of temperature and pressure effects

Author

Vandaele, A.C., Hermans, C., Fally, S., Carleer, M., Mérienne, M.-F., Jenouvrier, A., Coquart, B., and Colin, R.

Subjects
*ABSORPTION, *SPECTRUM analysis
Abstract

The measurements of the NO2 absorption cross sections by several authors have been considered in order to derive its temperature and pressure dependences in the 13 200–42 000 cm−1 spectral range. The temperature dependence is assumed to be linear in the temperature range investigated (217.0–298.5 K), whereas the influence of the total pressure is expressed as a temperature-dependent broadening coefficient. From measurements performed with mixtures of NO2 in air and in N2, values of γair0 (296 K) and γN20 (296 K) were found to be, respectively, 0.081±0.002 and 0.069±0.003 cm−1 atm−1. The temperature coefficient n obtained in the present work is 0.8±0.1. The parameterization of the cross sections developed in this work can reproduce measured cross sections within 4%. [Copyright &y& Elsevier]

Published
2003
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43. Line positions and energy levels of the 18O substitutions from the HDO/D2O spectra between 5600 and 8800cm−1

Author

Mikhailenko, S.N., Tashkun, S.A., Daumont, L., Jenouvrier, A., Carleer, M., Fally, S., and Vandaele, A.C.

Subjects
*ENERGY levels (Quantum mechanics), *RADIATIVE transfer, *ABSORPTION spectra, *INFRARED spectra, *FOURIER transform spectroscopy, *PHASE transitions
Abstract

Abstract: Absorption spectra of HDO/D2O mixtures recorded in the 5600–8800cm−1 region with a total pressure of water from 13 up to 18hPa and an absorption path length of 600m have been analyzed in order to obtain new spectroscopic data for HD18O and D2 18O. In spite of the low natural 18O concentration (about 2×10−3 with respect to the 16O one), about 1100 transitions belonging to HD18O and more than 280 transitions belonging to D2 18O have been assigned. Most of the D2 18O transitions belong to the ν 1+ν 2+ν 3 and 2ν 1+ν 3 bands. Sets of energy levels for seven vibrational states of D2 18O and four states of HD18O are reported for the first time. The comparison of the experimental data with the calculated values based on Partridge–Schwenke global variational calculations is discussed. [ABSTRACT FROM AUTHOR]

Published
2010
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44. Critical evaluation of measured rotation–vibration transitions and an experimental dataset of energy levels of HD18O

Author

Mikhailenko, S.N., Tashkun, S.A., Putilova, T.A., Starikova, E.N., Daumont, L., Jenouvrier, A., Fally, S., Carleer, M., Hermans, C., and Vandaele, A.C.

Subjects
*RADIATIVE transitions, *ENERGY levels (Quantum mechanics), *FOURIER transform spectroscopy, *ABSORPTION spectra, *VIBRATIONAL spectra
Abstract

Abstract: All available transitions from microwave to visible region (0.2–12 105cm−1) of the HD18O molecule were collected and tested using the RITZ computer code. Literature data were completed by transitions assigned to HD18O in long path Fourier transform absorption spectra of the H2O, HDO and D2O gas mixtures with natural abundance of oxygen-18. In addition about 40 unassigned lines between 4200 and 6600cm−1 of our previous water study associated with the HD18O molecule have been found and assigned. The new long path absorption spectra of the HDO and D2O mixtures allow us to observe about 1000 transitions of HD18O in the 6125–10720cm−1 spectral region. These data have been critically analyzed and used to obtain the most complete and precise set of the experimental energy levels of this molecule. [Copyright &y& Elsevier]

Published
2009
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45. HDO absorption spectrum above 11500cm−1: Assignment and dynamics

Author

Voronin, B.A., Naumenko, O.V., Carleer, M., Coheur, P.-F., Fally, S., Jenouvrier, A., Tolchenov, R.N., Vandaele, A.C., and Tennyson, J.

Subjects
*ABSORPTION spectra, *SPECTRUM analysis, *LASER spectroscopy, *MOLECULAR spectroscopy
Abstract

Abstract: Assignment of an HDO line list extracted from a recently measured H2O/HDO/D2O Fourier transform absorption spectrum recorded in the 11600–23000cm−1 region by Bach et al. (M. Bach, S. Fally, P.-F. Coheur, M. Carleer, A. Jenouvrier, A.C. Vandaele, J. Mol. Spectrosc. 232 (2005) 341–350.) is presented. More than 94% of the 3256 lines are given quantum number assignments and ascribed to line absorption by HDO; most of the remaining lines are actually due to D2O. High accuracy variational predictions of line positions and intensities are used for the spectral assignment process. Assignments to the ν 1 +5ν 3, 2ν 2 +5ν 3, ν 1 + ν 2 +3ν 3 and ν 1 +6ν 3 bands are presented for the first time. Comparisons are made with published ICLAS spectra covering the same spectral region and suggestions made for its recalibration. The results are used to illustrate the dynamical behaviour of highly excited vibrational states of HDO and to discuss previous vibrational assignments to high lying rotation–vibration states of this system. [Copyright &y& Elsevier]

Published
2007
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46. Combined analysis of the high sensitivity Fourier transform and ICLAS-VeCSEL absorption spectra of D2O between 8800 and 9520cm−1

Author

Naumenko, O.V., Leshchishina, O., Shirin, S., Jenouvrier, A., Fally, S., Vandaele, A.C., Bertseva, E., and Campargue, A.

Subjects
*ABSORPTION, *EXCITON theory, *INDUSTRIAL lasers, *POTENTIAL energy surfaces
Abstract

Abstract: The absorption spectrum of dideuterated water, D2O, has been recorded between 8800 and 9520cm−1 by intracavity laser absorption spectroscopy (ICLAS) based on a vertical external cavity system emitting laser (VeCSEL) and by high sensitivity Fourier Transform spectroscopy. The combined analysis of the spectra has allowed attributing 1223 transitions to the D2O species. The spectrum assignment was performed on the basis of the recent results of variational calculations based on an optimized potential energy surface of D2O. A set of 687 energy levels was derived from transitions assigned to eight upper vibrational states, 577 of them being reported for the first time. A detailed line list has been generated. The line intensities were retrieved mainly from the FTS spectrum and the absolute integrated intensities of the 2v 1 + v 2 + v 3 and the v 2 +3v 3 bands dominating the spectrum have been determined. [Copyright &y& Elsevier]

Published
2006
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48. Fourier Transform Spectroscopy of the O(2) Herzberg Bands.

Author

Jenouvrier A, Mérienne MF, Coquart B, Carleer M, Fally S, Vandaele AC, Hermans C, and Colin R

Abstract

The absorption spectra of the O(2) Herzberg band systems (A(3)Sigma(+)(u)-X(3)Sigma(-)(g), c(1)Sigma(-)(u)-X(3)Sigma(-)(g), and A' (3)Delta(u)-X(3)Sigma(-)(g)) lying in the wavelength region 240-300 nm were reinvestigated. The coupling of a long absorption cell and a high-resolution Fourier transform spectrometer has allowed the observation of numerous weak lines which were not reported previously. From the rotational analysis of the line positions, determined with an accuracy of 0.005 cm(-1), the molecular constants of the A(3)Sigma(+)(u), v = 0-12, c(1)Sigma(-)(u), v = 2-19, and A' (3)Delta(u), v = 2-12 levels are improved significantly. The interaction between the A and c states is described quantitatively. A new interpretation of the perturbations observed in the energy region close to the dissociation limit is given which involves a weakly bound (3)Pi(u) state as the most probable perturbing state. Copyright 1999 Academic Press.

Published
1999
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49. Absorption cross-sections of atmospheric constituents: NO2, O2, and H2O.

Author

Hermans C, Vandaele AC, Carleer M, Fally S, Colin R, Jenouvrier A, Coquart B, and Mérienne MF

Abstract

Absorption spectroscopy, which is widely used for concentration measurements of tropospheric and stratospheric compounds, requires precise values of the absorption cross-sections of the measured species. NO(2), O(2) and its collision-induced absorption spectrum, and H(2)O absorption cross-sections have been measured at temperature and pressure conditions prevailing in the Earth's atmosphere. Corrections to the generally accepted analysis procedures used to resolve the convolution problem are also proposed.

Published
1999
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