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Register a new userCS Depletion in Prestellar Cores
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The CS molecule is known to be absorbed onto dust in the cold and dense conditions, causing it to get significantly depleted in the central region of cores. This study is aimed to investigate the depletion of the CS molecule using the optically thin C$^{34}$S molecular line observations. We mapped five prestellar cores, L1544, L1552, L1689B, L694-2, and L1197 using two molecular lines, C$^{34}$S $(J=2-1)$ and N$_2$H$^+$ $(J=1-0)$ with the NRO 45-m telescope, doubling the number of cores where the CS depletion was probed using C$^{34}$S. In most of our targets, the distribution of C$^{34}$S emission shows features that suggest that the CS molecule is generally depleted in the center of the prestellar cores. The radial profile of the CS abundance with respect to H$_2$ directly measured from the CS emission and the Herschel dust emission indicates that the CS molecule is depleted by a factor of $sim$3 toward the central regions of the cores with respect to their outer regions. The degree of the depletion is found to be even more enhanced by an order of magnitude when the contaminating effect introduced by the presence of CS molecules in the surrounding envelope that lie along the line-of-sight is removed. Except for L1197 which is classified as relatively the least evolved core in our targets based on its observed physical parameters, we found that the remaining four prestellar cores are suffering from significant CS depletion at their central region regardless of the relative difference in their evolutionary status.
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Young massive stars are usually found embedded in dense massive molecular clumps and are known for being highly obscured and distant. During their formation process, deuteration is regarded as a potentially good indicator of the very early formation stages. In this work, we test the observability of the ground-state transition of ortho-H$_2$D$^+$ $J_{rm {K_a, K_c}} = 1_{10}$-$1_{11} $ by performing interferometric and single-dish synthetic observations using magneto-hydrodynamic simulations of high-mass collapsing molecular cores, including deuteration chemistry. We studied different evolutionary times and source distances (from 1 to 7 kpc) to estimate the information loss when comparing the column densities inferred from the synthetic observations to the column densities in the model. We mimicked single-dish observations considering an APEX-like beam and interferometric observations using CASA and assuming the most compact configuration for the ALMA antennas. We found that, for centrally concentrated density distributions, the column densities are underestimated by about 51% in the case of high-resolution ALMA observations ($leqslant$1) and up to 90% for APEX observations (17). Interferometers retrieve values closer to the real ones, however, their finite spatial sampling results in the loss of contribution from large-scale structures due to the lack of short baselines. We conclude that, the emission of o-H$_2$D$^+$ in distant massive dense cores is faint and would require from $sim$1 to $sim$7 hours of observation at distances of 1 and 7 kpc, respectively, to achieve a 14$sigma$ detection in the best case scenario. Additionally, the column densities derived from such observations will certainly be affected by beam dilution in the case of single-dishes and spatial filtering in the case of interferometers.
We report the detection of D2CO in a sample of starless dense cores, in which we previously measured the degree of CO depletion. The deuterium fractionation is found extremely high, [D2CO]/[H2CO] ~ 1-10 %, similar to that reported in low-mass protostars. This provides convincing evidence that D2CO is formed in the cold pre-stellar cores, and later desorbed when the gas warms up in protostars. We find that the cores with the highest CO depletions have also the largest [D2CO]/[H2CO] ratios, supporting the theoretical prediction that deuteration increases with increasing CO depletion.
We study the abundance of CCH in prestellar cores both because of its role in the chemistry and because it is a potential probe of the magnetic field. We also consider the non-LTE behaviour of the N=1-0 and N=2-1 transitions of CCH and improve current estimates of the spectroscopic constants of CCH. We used the IRAM 30m radiotelescope to map the N=1-0 and N=2-1 transitions of CCH towards the prestellar cores L1498 and CB246. Towards CB246, we also mapped the 1.3 mm dust emission, the J=1-0 transition of N2H+ and the J=2-1 transition of C18O. We used a Monte Carlo radiative transfer program to analyse the CCH observations of L1498. We derived the distribution of CCH column densities and compared with the H2 column densities inferred from dust emission. We find that while non-LTE intensity ratios of different components of the N=1-0 and N=2-1 lines are present, they are of minor importance and do not impede CCH column density determinations based upon LTE analysis. Moreover, the comparison of our Monte-Carlo calculations with observations suggest that the non-LTE deviations can be qualitatively understood. For L1498, our observations in conjunction with the Monte Carlo code imply a CCH depletion hole of radius 9 x 10^{16} cm similar to that found for other C-containing species. We briefly discuss the significance of the observed CCH abundance distribution. Finally, we used our observations to provide improved estimates for the rest frequencies of all six components of the CCH(1-0) line and seven components of CCH(2-1). Based on these results, we compute improved spectroscopic constants for CCH. We also give a brief discussion of the prospects for measuring magnetic field strengths using CCH.
The recent unexpected detection of terrestrial complex organic molecules in the cold (~ 10 K) gas has cast doubts on the commonly accepted formation mechanisms of these species. Standard gas-phase mechanisms are inefficient and tend to underproduce these molecules, and many of the key reactions involved are unconstrained. Grain-surface mechanisms, which were presented as a viable alternative, suffer from the fact that they rely on grain surface diffusion of heavy radicals, which is not possible thermally at very low temperatures. One of the simplest terrestrial complex organic molecules, methanol is believed to form on cold grain surfaces following from successive H atom additions on CO. Unlike heavier species, H atoms are very mobile on grain surfaces even at 10 K. Intermediate species involved in grain surface methanol formation by CO hydrogenation are the radicals HCO and CH3O, as well as the stable species formaldehyde H2CO. These radicals are thought to be precursors of complex organic molecules on grain surfaces. We present new observations of the HCO and CH3O radicals in a sample of prestellar cores and carry out an analysis of the abundances of the species HCO, H2CO, CH3O, and CH3OH, which represent the various stages of grain-surface hydrogenation of CO to CH3OH. The abundance ratios between the various intermediate species in the hydrogenation reaction of CO on grains are similar in all sources of our sample, HCO:H2CO:CH3O:CH3OH ~ 10:100:1:100. We argue that these ratios may not be representative of the primordial abundances on the grains but, rather, suggest that the radicals HCO and CH3O are gas-phase products of the precursors H2CO and CH3OH, respectively. Gas-phase pathways are considered and simple estimates of HCO and CH3O abundances are compared to the observations. Critical reaction rate constants, branching ratios, and intermediate species are finally identified.
We studied the abundance of HCN, H13CN, and HN13C in a sample of prestellar cores, in order to search for species associated with high density gas. We used the IRAM 30m radiotelescope to observe along the major and the minor axes of L1498, L1521E, and TMC 2, three cores chosen on the basis of their CO depletion properties. We mapped the J=1-0 transition of HCN, H13CN, and HN13C towards the source sample plus the J=1-0 transition of N2H+ and the J=2-1 transition of C18O in TMC 2. We used two different radiative transfer codes, making use of recent collisional rate calculations, in order to determine more accurately the excitation temperature, leading to a more exact evaluation of the column densities and abundances. We find that the optical depths of both H13CN(1-0) and HN13C(1-0) are non-negligible, allowing us to estimate excitation temperatures for these transitions in many positions in the three sources. The observed excitation temperatures are consistent with recent computations of the collisional rates for these species and they correlate with hydrogen column density inferred from dust emission. We conclude that HCN and HNC are relatively abundant in the high density zone, n(H2) about 10^5 cm-3, where CO is depleted. The relative abundance [HNC]/[HCN] differs from unity by at most 30 per cent consistent with chemical expectations. The three hyperfine satellites of HCN(1-0) are optically thick in the regions mapped, but the profiles become increasingly skewed to the blue (L1498 and TMC 2) or red (L1521E) with increasing optical depth suggesting absorption by foreground layers.
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