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Context. The chemistry of sulphur-bearing species in the interstellar medium remains poorly understood, but might play a key role in the chemical evolution of star-forming regions. Aims. Coupling laboratory experiments to observations of sulphur-bearing species in different parts of star-forming regions, we aim to understand the chemical behavior of the sulphur species in cold and warm regions of protostars, and we ultimately hope to connect them. Methods. We performed laboratory experiments in which we tested the reactivity of hydrogen sulfide (H2S) on a cold substrate with hydrogen and/or carbon monoxide (CO) under different physical conditions that allowed us to determine the products from sulphur reactions using a quadrupole mass spectrometer. The laboratory experiments were complemented by observations. We observed two luminous binary sources in the Cygnus-X star-forming complex, Cygnus X-N30 and N12, covering a frequency range of 329-361 GHz at a spatial resolution of 1 '' 5 with the SubMillimeter Array (SMA). This study was complemented by a 3 mm line survey of Cygnus X-N12 covering specific frequency windows in the frequency ranges 72.0-79.8 GHz at a spatial resolution of 34 '' 0-30 '' 0 and 84.2-115.5 GHz at a spatial resolution of 29 '' 0-21 '' 0, with the IRAM-30 m single-dish telescope. Column densities and excitation temperatures were derived under the local thermodynamic equilibrium approximation. Results. We find that OCS is a direct product from H2S reacting with CO and H under cold temperatures (T < 100 K) from laboratory experiments. OCS is therefore found to be an important solid-state S-reservoir. We identify several S-species in the cold envelope of Cyg X-N12, principally organo-sulphurs (H2CS, CS, OCS, CCS, C3S, CH3SH, and HSCN). For the hot cores of Cyg X-N12 and N30, only OCS, CS and H2CS were detected. We found a difference in the S-diversity between the hot core and the cold envelope of N12, which is likely due to the sensitivity of t

Gas phase Elemental abundances in Molecular CloudS (GEMS) is an IRAM 30 m Large Program designed to provide estimates of the S, C, N, and O depletions and gas ionization degree, X(e(-)), in a selected set of star-forming filaments of Taurus, Perseus, and Orion. Our immediate goal is to build up a complete and large database of molecular abundances that can serve as an observational basis for estimating X(e(-)) and the C, O, N, and S depletions through chemical modeling. We observed and derived the abundances of 14 species ((CO)-C-13, (CO)-O-18, HCO+, (HCO+)-C-13, (HCO+)-O-18, HCN, (HCN)-C-13, HNC, HCS+, CS, SO, (SO)-S-34, H2S, and OCS) in 244 positions, covering the A(V) similar to 3 to similar to 100 mag, n(H-2) similar to a few 10(3) to 10(6) cm(-3), and T-k similar to 10 to similar to 30 K ranges in these clouds, and avoiding protostars, HII regions, and bipolar outflows. A statistical analysis is carried out in order to identify general trends between different species and with physical parameters. Relations between molecules reveal strong linear correlations which define three different families of species: (1) (CO)-C-13 and (CO)-O-18 isotopologs; (2) (HCO+)-C-13, (HCO+)-O-18, H-13 CN, and HNC; and (3) the S-bearing molecules. The abundances of the CO isotopologs increase with the gas kinetic temperature until T-K similar to 15 K. For higher temperatures, the abundance remains constant with a scatter of a factor of similar to 3. The abundances of H-13 CO+, HC18 O+, H-13 CN, and HNC are well correlated with each other, and all of them decrease with molecular hydrogen density, following the law proportional to n(H-2)(-0.8 +/- 0.2). The abundances of S-bearing species also decrease with molecular hydrogen density at a rate of (S-bearing/H)(gas) proportional to n(H-2)(-0.6 +/- 0.1). The abundances of molecules belonging to groups 2 and 3 do not present any clear trend with gas temperature. At scales of molecular clouds, the (CO)-O-18 abundance is the quantity that

Context. Carbon monosulphide (CS) is among the most abundant gas-phase S-bearing molecules in cold dark molecular clouds. It is easily observable with several transitions in the millimeter wavelength range, and has been widely used as a tracer of the gas density in the interstellar medium in our Galaxy and external galaxies. However, chemical models fail to account for the observed CS abundances when assuming the cosmic value for the elemental abundance of sulfur. Aims. The CS+O -> CO + S reaction has been proposed as a relevant CS destruction mechanism at low temperatures, and could explain the discrepancy between models and observations. Its reaction rate has been experimentally measured at temperatures of 150-400 K, but the extrapolation to lower temperatures is doubtful. Our goal is to calculate the CS+O reaction rate at temperatures <150 K which are prevailing in the interstellar medium. Methods. We performed ab initio calculations to obtain the three lowest potential energy surfaces (PES) of the CS+O system. These PESs are used to study the reaction dynamics, using several methods (classical, quantum, and semiclassical) to eventually calculate the CS + O thermal reaction rates. In order to check the accuracy of our calculations, we compare the results of our theoretical calculations for T similar to 150-400 K with those obtained in the laboratory. Results. Our detailed theoretical study on the CS+O reaction, which is in agreement with the experimental data obtained at 150-400 K, demonstrates the reliability of our approach. After a careful analysis at lower temperatures, we find that the rate constant at 10 K is negligible, below 10(-15) cm(3) s(-1), which is consistent with the extrapolation of experimental data using the Arrhenius expression. Conclusions. We use the updated chemical network to model the sulfur chemistry in Taurus Molecular Cloud 1 (TMC 1) based on molecular abundances determined from Gas phase Elemental abundances in Molecular CloudS (GEMS)

Gas phase Elemental abundances in Molecular CloudS (GEMS) is an IRAM 30 m Large Program designed to provide estimates of the S, C, N, and O depletions and gas ionization degree, X(e-), in a selected set of star-forming filaments of Taurus, Perseus, and Orion. Our immediate goal is to build up a complete and large database of molecular abundances that can serve as an observational basis for estimating X(e-) and the C, O, N, and S depletions through chemical modeling. We observed and derived the abundances of 14 species (13CO, C18O, HCO+, H13CO+, HC18O+, HCN, H13CN, HNC, HCS+, CS, SO, 34SO, H2S, and OCS) in 244 positions, covering the AV ~3 to ~100 mag, n(H2) ~ a few 103 to 106 cm-3, and Tk ~10 to ~30 K ranges in these clouds, and avoiding protostars, HII regions, and bipolar outflows. A statistical analysis is carried out in order to identify general trends between different species and with physical parameters. Relations between molecules reveal strong linear correlations which define three different families of species: (1) 13CO and C18O isotopologs; (2) H13CO+, HC18O+, H13 CN, and HNC; and (3) the S-bearing molecules. The abundances of the CO isotopologs increase with the gas kinetic temperature until TK ~ 15 K. For higher temperatures, the abundance remains constant with a scatter of a factor of ~3. The abundances of H13 CO+, HC18 O+, H13 CN, and HNC are well correlated with each other, and all of them decrease with molecular hydrogen density, following the law ∝ n(H2)-0.8 ± 0.2. The abundances of S-bearing species also decrease with molecular hydrogen density at a rate of (S-bearing/H)gas ∝ n(H2)-0.6 ± 0.1. The abundances of molecules belonging to groups 2 and 3 do not present any clear trend with gas temperature. At scales of molecular clouds, the C18O abundance is the quantity that better correlates with the cloud mass. We discuss the utility of the 13CO/C18O, HCO+/H13CO+, and H13 CO+/H13CN abundance ratios as chemical diagnostics of star formation in e, Astrodynamics & Space Missions

Context. Sulphur is one of the most abundant elements in the Universe. Surprisingly, sulphuretted molecules are not as abundant as expected in the interstellar medium and the identity of the main sulphur reservoir is still an open question.Aims. Our goal is to investigate the H2S chemistry in dark clouds, as this stable molecule is a potential sulphur reservoir.Methods. Using millimeter observations of CS, SO, H2S, and their isotopologues, we determine the physical conditions and H2S abundances along the cores TMC 1-C, TMC 1-CP, and Barnard 1b. The gas-grain model NAUTILUS is used to model the sulphur chemistry and explore the impact of photo-desorption and chemical desorption on the H2S abundance.Results. Our modeling shows that chemical desorption is the main source of gas-phase H2S in dark cores. The measured H2S abundance can only be fitted if we assume that the chemical desorption rate decreases by more than a factor of 10 when n(H) > 2 x 10(4). This change in the desorption rate is consistent with the formation of thick H2O and CO ice mantles on grain surfaces. The observed SO and H2S abundances are in good agreement with our predictions adopting an undepleted value of the sulphur abundance. However, the CS abundance is overestimated by a factor of 5-10. Along the three cores, atomic S is predicted to be the main sulphur reservoir.Conclusions. The gaseous H2S abundance is well reproduced, assuming undepleted sulphur abundance and chemical desorption as the main source of H2S. The behavior of the observed H2S abundance suggests a changing desorption efficiency, which would probe the snowline in these cold cores. Our model, however, highly overestimates the observed gas-phase CS abundance. Given the uncertainty in the sulphur chemistry, we can only conclude that our data are consistent with a cosmic elemental S abundance with an uncertainty of a factor of 10.

Sulphur is one of the most abundant elements in the Universe. Surprisingly, sulphuretted molecules are not as abundant as expected in the interstellar medium and the identity of the main sulphur reservoir is still an open question. Our goal is to investigate the H S chemistry in dark clouds, as this stable molecule is a potential sulphur reservoir. Using millimeter observations of CS, SO, H S, and their isotopologues, we determine the physical conditions and H S abundances along the cores TMC 1-C, TMC 1-CP, and Barnard 1b. The gas-grain model Nautilus is used to model the sulphur chemistry and explore the impact of photo-desorption and chemical desorption on the H S abundance. Our modeling shows that chemical desorption is the main source of gas-phase H S in dark cores. The measured H S abundance can only be fitted if we assume that the chemical desorption rate decreases by more than a factor of 10 when > 2 × 10 . This change in the desorption rate is consistent with the formation of thick H O and CO ice mantles on grain surfaces. The observed SO and H S abundances are in good agreement with our predictions adopting an undepleted value of the sulphur abundance. However, the CS abundance is overestimated by a factor of 5 - 10. Along the three cores, atomic S is predicted to be the main sulphur reservoir. The gaseous H S abundance is well reproduced, assuming undepleted sulphur abundance and chemical desorption as the main source of H S. The behavior of the observed H S abundance suggests a changing desorption efficiency, which would probe the snowline in these cold cores. Our model, however, highly overestimates the observed gas-phase CS abundance. Given the uncertainty in the sulphur chemistry, we can only conclude that our data are consistent with a cosmic elemental S abundance with an uncertainty of a factor of 10.

We present Atacama Large Millimeter/submillimeter Array maps of the starless molecular cloud core Ophiuchus/H-MM1 in the lines of deuterated ammonia (ortho-NH2 D), methanol (CH3 OH), and sulfur monoxide (SO). The dense core is seen in NH2 D emission, whereas the CH3 OH and SO distributions form a halo surrounding the core. Because methanol is formed on grain surfaces, its emission highlights regions where desorption from grains is particularly efficient. Methanol and sulfur monoxide are most abundant in a narrow zone that follows the eastern side of the core. This side is sheltered from the stronger external radiation field coming from the west. We show that photodissociation on the illuminated side can give rise to an asymmetric methanol distribution but that the stark contrast observed in H-MM1 is hard to explain without assuming enhanced desorption on the shaded side. The region of the brightest emission has a wavy structure that rolls up at one end. This is the signature of Kelvin-Helmholtz instability occurring in sheared flows. We suggest that in this zone, methanol and sulfur are released as a result of grain-grain collisions induced by shear vorticity. © 2020. The American Astronomical Society. All rights reserved.

Context. Sulphur is one of the most abundant elements in the Universe. Surprisingly, sulphuretted molecules are not as abundant as expected in the interstellar medium and the identity of the main sulphur reservoir is still an open question. Aims. Our goal is to investigate the H2S chemistry in dark clouds, as this stable molecule is a potential sulphur reservoir. Methods. Using millimeter observations of CS, SO, H2S, and their isotopologues, we determine the physical conditions and H2S abundances along the cores TMC 1-C, TMC 1-CP, and Barnard 1b. The gas-grain model NAUTILUS is used to model the sulphur chemistry and explore the impact of photo-desorption and chemical desorption on the H2S abundance. Results. Our modeling shows that chemical desorption is the main source of gas-phase H2S in dark cores. The measured H2S abundance can only be fitted if we assume that the chemical desorption rate decreases by more than a factor of 10 when nH > 2 × 104. This change in the desorption rate is consistent with the formation of thick H2O and CO ice mantles on grain surfaces. The observed SO and H2S abundances are in good agreement with our predictions adopting an undepleted value of the sulphur abundance. However, the CS abundance is overestimated by a factor of 5-10. Along the three cores, atomic S is predicted to be the main sulphur reservoir. Conclusions. The gaseous H2S abundance is well reproduced, assuming undepleted sulphur abundance and chemical desorption as the main source of H2S. The behavior of the observed H2S abundance suggests a changing desorption efficiency, which would probe the snowline in these cold cores. Our model, however, highly overestimates the observed gas-phase CS abundance. Given the uncertainty in the sulphur chemistry, we can only conclude that our data are consistent with a cosmic elemental S abundance with an uncertainty of a factor of 10.

Context. AB Aur is a Herbig Ae star that hosts a prototypical transition disk. The disk shows a plethora of features connected with planet formation mechanisms, such as spiral arms, dust cavities, and dust traps. Understanding the physical and chemical characteristics of these features is crucial to advancing our knowledge of the planet formation processes. Aims. We aim to characterize the gaseous disk around the Herbig Ae star AB Aur. A complete spectroscopic study was performed using NOEMA to determine the physical and chemical conditions with high spatial resolution. Methods. We present new NOrthern Extended Millimeter Array (NOEMA) interferometric observations of the continuum and (CO)-C-12, (CO)-C-13, (CO)-O-18, H2CO, and SO lines obtained at high resolution. We used the integrated intensity maps and stacked spectra to derive reliable estimates of the disk temperature. By combining our (CO)-C-13 and (CO)-O-18 observations, we computed the gas-to-dust ratio along the disk. We also derived column density maps for the different species and used them to compute abundance maps. The results of our observations were compared with a set of Nautilus astrochemical models to obtain insight into the disk properties. Results. We detected continuum emission in a ring that extends from 0.6 '' to similar to 2.0 '', peaking at 0.97 '' and with a strong azimuthal asymmetry. The molecules observed show different spatial distributions, and the peaks of the distributions are not correlated with the binding energy. Using H2CO and SO lines, we derived a mean disk temperature of 39 K. We derived a gas-to-dust ratio that ranges from 10 to 40 along the disk. Abundance with respect to (CO)-C-13 for SO (similar to 2 x 10(-4)) is almost one order of magnitude greater than the value derived for H2CO (1.6 x 10(-5)). The comparison with Nautilus models favors a disk with a low gas-to-dust ratio (40) and prominent sulfur depletion. Conclusions. From a very complete spectroscopic study of the p

Context. Sulphur is one of the most abundant elements in the Universe (S/H ~ 1.3 × 10) and plays a crucial role in biological systems on Earth. The understanding of its chemistry is therefore of major importance. Aims. Our goal is to complete the inventory of S-bearing molecules and their abundances in the prototypical photodissociation region (PDR) the Horsehead nebula to gain insight into sulphur chemistry in UV irradiated regions. Based on the WHISPER (Wide-band High-resolution Iram-30 m Surveys at two positions with Emir Receivers) millimeter (mm) line survey, our goal is to provide an improved and more accurate description of sulphur species and their abundances towards the core and PDR positions in the Horsehead. Methods. The Monte Carlo Markov chain (MCMC) methodology and the molecular excitation and radiative transfer code RADEX were used to explore the parameter space and determine physical conditions and beam-averaged molecular abundances. Results. A total of 13 S-bearing species (CS, SO, SO, OCS, HCS-both ortho and para-HDCS, CS, HCS, SO, HS, SH, NS and NS) have been detected in the two targeted positions. This is the first detection of SO in the Horsehead and the first detection of NS in any PDR. We find a differentiated chemical behaviour between C-S and O-S bearing species within the nebula. The C-S bearing species CS and o-HCS present fractional abundances a factor of > two higher in the core than in the PDR. In contrast, the O-S bearing molecules SO, SO, and OCS present similar abundances towards both positions. A few molecules, SO, NS, and NS, are more abundant towards the PDR than towards the core, and could be considered as PDR tracers. Conclusions. This is the first complete study of S-bearing species towards a PDR. Our study shows that CS, SO, and HS are the most abundant S-bearing molecules in the PDR with abundances of approximately a few 10. We recall that SH, SH, S, and S are not observable at the wavelengths covered by the WHISPER survey. A