arXiv subjects

A. Campargue

Publications and source records attributed to A. Campargue.

7 recordsLinked to original sources

arXiv2026

The HITRAN2024 methane update

Spectroscopic parameters of methane from many different studies were gathered to improve the HITRAN database towards its 2024 version. After a validation process using high-resolution FTS and CRDS spectra, about 80,000 lines of the four most abundant isotopologues were replaced from the dyad to the triacontad regions. These changes amount to 51,000 transition wavenumbers, 18,000 line intensities, 33,000 pressure-broadening half-widths, and 3300 assignments. 44,000 new lines were added with 16,000 old lines removed, extending the database from 12,000 cm$^{-1}$ up to 14,000 cm$^{-1}$, and covering some gaps. A greater focus was brought on the pentad, octad, and tetradecad regions, targeted by several remote sensing instruments. In these regions, comparisons of spectral fits from multiple line lists were performed, taking only the parameters that provide best fit for each line. In the $ν_3$ band, in addition to replacing the previous values, speed-independent pressure broadening parameters of $^{12}$CH$_4$ were gathered and used to fit Padé-approximant functions. These functions then replaced any outdated experimental data in $ν_3$, missing data in the new lines, as well as the values that were determined to be outside their physical boundaries. The CH$_3$D broadening parameters were replaced in the same manner, for missing and low or high values, using a semi-empirical formula instead.

astro-ph.EP↗

arXiv2025

SpeCT: A state-of-the-art tool to calculate correlated-k tables and continua of CO$_2$-H$_2$O-N$_2$ gas mixtures

A key challenge in modeling (exo)planetary atmospheres lies in generating extensive opacity datasets that cover the wide variety of possible atmospheric composition, pressure, and temperature conditions. This critical step requires specific knowledge and can be considerably time-consuming. To circumvent this issue, most available codes approximate the total opacity by summing the contributions of individual molecular species during the radiative transfer calculation. This approach neglects inter-species interactions, which can be an issue for precisely estimating the climate of planets. To produce accurate opacity data, such as correlated-k tables, chi factor corrections of the far-wings of the line profile are required. We propose an update of the chi factors of CO$_2$ absorption lines that are relevant for terrestrial planets (pure CO$_2$, CO$_2$-N$_2$ and CO$_2$-H$_2$O). These new factors are already implemented in an original user-friendly open-source tool designed to calculate high resolution spectra, named SpeCT. The latter enables to produce correlated-k tables for mixtures made of H$_2$O, CO$_2$ and N$_2$, accounting for inter-species broadening. In order to facilitate future updates of these chi factors, we also provide a review of all the relevant laboratory measurements available in the literature for the considered mixtures. Finally, we provide in this work 8 different correlated-k tables and continua for pure CO$_2$, CO$_2$-N$_2$, CO$_2$-H$_2$O and CO$_2$-H$_2$O-N$_2$ mixtures based on the MT_CKD formalism (for H$_2$O), and calculated using SpeCT. These opacity data can be used to study various planets and atmospheric conditions, such as Earth's paleo-climates, Mars, Venus, Magma ocean exoplanets, telluric exoplanets.

astro-ph.EP↗

arXiv2025

New beyond-Voigt line-shape profile recommended for the HITRAN database

Parameters associated with the collisional perturbation of spectral lines are essential for modeling the absorption of electromagnetic radiation in gas media. The HITRAN molecular spectroscopic database provides these parameters, although originally they were associated only with the Voigt profile parameterization. However, in the HITRAN2016 and HITRAN2020 editions, Voigt, speed-dependent Voigt and Hartmann-Tran (HT) profiles have been incorporated, thanks to the new relational structure of the database. The HT profile was introduced in HITRAN in 2016 as a recommended profile for the most accurate spectral interpretations and modeling. It was parameterized with a four-temperature-range temperature dependence. Since then, however, some features of the HT profile have been revealed that are problematic from a practical perspective. These are: the singular behavior of the temperature dependencies of the velocity-changing parameters when the shift parameter crosses zero and the difficulty in evaluating the former for mixtures. In this article, we summarize efforts to eliminate the above-mentioned problems that led us to recommend using the quadratic speed-dependent hard-collision (qSDHC) profile with double-power-law (DPL) temperature dependencies. We refer to this profile as a modified Hartmann-Tran (mHT) profile. The computational cost of evaluating it is the same as for the HT profile. We give a detailed description of the mHT profile (also including line mixing) and discuss the representation of its parameters, together with their DPL temperature parametrization adopted in the HITRAN database. We discuss an efficient algorithm for evaluating this profile and provide corresponding computer codes in several programming languages: Fortran, Python, MATLAB, Wolfram Mathematica, and LabVIEW. We also discuss the associated update of the HITRAN Application Programming Interface (HAPI).

physics.atom-ph↗

arXiv2024

Room temperature detection of the (H2)2 dimer

The hydrogen dimer, (H2)2, is among the most weakly bound van der Waals complexes and a prototype species for first principles ab initio studies. The detection of the (H2)2 infrared absorption spectrum was reported more than thirty years ago at a temperature of 20 K. Due to the sharp decrease of the (H2)2 abundance with temperature, a detection at room temperature was generally considered as hardly achievable. Here we report the first room temperature detection of partly resolved rotational structures of (H2)2 by cavity ring down spectroscopy at sub-atmospheric pressures, in the region of the first overtone band of H2 near 1.2 micron. The quantitative analysis of the absorption features observed around ten allowed or forbidden transition frequencies of the monomer provides insight on the structure of this elusive species and a benchmark for future theoretical studies.

physics.chem-ph↗

arXiv2016

A near infrared line list for \NH: Analysis of a Kitt Peak spectrum after 35 years

A Fourier Transform (FT) absorption spectrum of room temperature NH3 in the region 7400 - 8600 cm-1 is analysed using a variational line list and ground state energies determined using the MARVEL procedure. The spectrum was measured by Dr Catherine de Bergh in 1980 and is available from the Kitt Peak data center. The centers and intensities of 8468 ammonia lines were retrieved using a multiline fitting procedure. 2474 lines are assigned to 21 bands providing 1692 experimental energies in the range 7000 - 9000 cm-1. The spectrum was assigned by the joint use of the BYTe variational line list and combination differences. The assignments and experimental energies presented in this work are the first for ammonia in the region 7400 - 8600 cm-1, considerably extending the range of known vibrational-excited states

physics.chem-ph↗

arXiv2014

High sensitivity Cavity Ring Down spectroscopy of 18O enriched carbon dioxide between 5850 and 7000 cm-1: Part III-Analysis and theoretical modeling of the 12C17O2, 16O12C17O, 17O12C18O, 16O13C17O and 17O13C18O spectra

More than 19,700 transitions belonging to 11 isotopologues of carbon dioxide have been assigned in the room temperature absorption spectrum of highly 18O enriched carbon dioxide recorded by very high sensitivity CW-Cavity Ring Down spectroscopy between 5851 and 6990 cm-1 (1.71-1.43 \mum). This third and last report is devoted to the analysis of the bands of five 17O containing isotopologues present at very low concentration in the studied spectra: 16O12C17O, 17O12C18O, 16O13C17O, 17O13C18O and 12C17O2 (627, 728, 637, 738 and 727 in short hand notation). On the basis of the predictions of effective Hamiltonian models, a total of 1759, 1786, 335, 273 and 551 transitions belonging to 24, 24, 5, 4 and 7 bands were rovibrationally assigned for 627, 728, 637, 738 and 727, respectively. For comparison, only five bands were previously measured in the region for the 728 species. All the identified bands belong to the \deltaP=8 and 9 series of transitions, where P=2V1+V2+3V3 is the polyad number (Vi are vibrational quantum numbers). The band-by-band analysis has allowed deriving accurate spectroscopic parameters of 61 bands from a fit of the measured line positions. Two interpolyad resonance perturbations were identified.

physics.atom-ph↗

arXiv2009

Pluto's lower atmosphere structure and methane abundance from high-resolution spectroscopy and stellar occultations

Context: Pluto possesses a thin atmosphere, primarily composed of nitrogen, in which the detection of methane has been reported. Aims: The goal is to constrain essential but so far unknown parameters of Pluto's atmosphere such as the surface pressure, lower atmosphere thermal stucture, and methane mixing ratio. Methods: We use high-resolution spectroscopic observations of gaseous methane, and a novel analysis of occultation light-curves. Results: We show that (i) Pluto's surface pressure is currently in the 6.5-24 microbar range (ii) the methane mixing ratio is 0.5+/-0.1 %, adequate to explain Pluto's inverted thermal structure and ~100 K upper atmosphere temperature (iii) a troposphere is not required by our data, but if present, it has a depth of at most 17 km, i.e. less than one pressure scale height; in this case methane is supersaturated in most of it. The atmospheric and bulk surface abundance of methane are strikingly similar, a possible consequence of the presence of a CH4-rich top surface layer.

astro-ph.EP↗