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Register a new userConstraining the abundances of complex organics in the inner regions of solar-type protostars
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The high abundances of Complex Organic Molecules (COMs) with respect to methanol, the most abundant COM, detected towards low-mass protostars, tend to be underpredicted by astrochemical models. This discrepancy might come from the large beam of the single-dish telescopes, encompassing several components of the studied protostar, commonly used to detect COMs. To address this issue, we have carried out multi-line observations of methanol and several COMs towards the two low-mass protostars NGC1333-IRAS2A and -IRAS4A with the Plateau de Bure interferometer at an angular resolution of 2 arcsec, resulting in the first multi-line detection of the O-bearing species glycolaldehyde and ethanol and of the N-bearing species ethyl cyanide towards low-mass protostars other than IRAS 16293. The high number of detected transitions from COMs (more than 40 methanol transitions for instance) allowed us to accurately derive the source size of their emission and the COMs column densities. The COMs abundances with respect to methanol derived towards IRAS2A and IRAS4A are slightly, but not substantitally, lower than those derived from previous single-dish observations. The COMs abundance ratios do not vary significantly with the protostellar luminosity, over five orders of magnitude, implying that low-mass hot corinos are quite chemically rich as high-mass hot cores. Astrochemical models still underpredict the abundances of key COMs, such as methyl formate or di-methyl ether, suggesting that our understanding of their formation remains incomplete.
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The [HDO]/[H2O] ratio is a crucial parameter for probing the history of water formation. So far, it has been measured for only three solar type protostars and yielded different results, possibly pointing to a substantially different history in their formation. In the present work, we report new interferometric observations of the HDO 4 2,2 - 4 2,3 line for two solar type protostars, IRAS2A and IRAS4A, located in the NGC1333 region. In both sources, the detected HDO emission originates from a central compact unresolved region. Comparison with previously published interferometric observations of the H218$O 3 1,3 - 2 2,0 line shows that the HDO and H$_2$O lines mostly come from the same region. A non-LTE LVG analysis of the HDO and H218$O line emissions, combined with published observations, provides a [HDO]/[H2O] ratio of 0.3 - 8 % in IRAS2A and 0.5 - 3 % in IRAS4A. First, the water fractionation is lower than that of other molecules such as formaldehyde and methanol in the same sources. Second, it is similar to that measured in the solar type protostar prototype, IRAS16293-2422, and, surprisingly enough, larger than that measured in NGC1333 IRAS4B. {The comparison of the measured values towards IRAS2A and IRAS4A with the predictions of our gas-grain model GRAINOBLE gives similar conclusions to those for IRAS 16293, arguing that these protostars {share} a similar chemical history, although they are located in different clouds.
Deuterium-to-hydrogen (D/H) enrichments in molecular species provide clues about their original formation environment. The organic materials in primitive solar system bodies have generally higher D/H ratios and show greater D/H variation when compared to D/H in solar system water. We propose this difference arises at least in part due to 1) the availability of additional chemical fractionation pathways for organics beyond that for water, and 2) the higher volatility of key carbon reservoirs compared to oxygen. We test this hypothesis using detailed disk models, including a sophisticated, new disk ionization treatment with a low cosmic ray ionization rate, and find that disk chemistry leads to higher deuterium enrichment in organics compared to water, helped especially by fractionation via the precursors CH$_2$D$^+$/CH$_3^+$. We also find that the D/H ratio in individual species varies significantly depending on their particular formation pathways. For example, from $sim20-40$ AU, CH$_4$ can reach $rm{D/Hsim2times10^{-3}}$, while D/H in CH$_3$OH remains locally unaltered. Finally, while the global organic D/H in our models can reproduce intermediately elevated D/H in the bulk hydrocarbon reservoir, our models are unable to reproduce the most deuterium-enriched organic materials in the solar system, and thus our model requires some inheritance from the cold interstellar medium from which the Sun formed.
Complex organics are now commonly found in meteorites, comets, asteroids, planetary satellites, and interplanetary dust particles. The chemical composition and possible origin of these organics are presented. Specifically, we discuss the possible link between Solar System organics and the complex organics synthesized during the late stages of stellar evolution. Implications of extraterrestrial organics on the origin of life on Earth and the possibility of existence of primordial organics on Earth are also discussed.
Methanol is a key species in astrochemistry since it is the most abundant organic molecule in the ISM and is thought to be the mother molecule of many complex organic species. Estimating the deuteration of methanol around young protostars is of crucial importance because it highly depends on its formation mechanisms and the physical conditions during its moment of formation. We analyse dozens of transitions from deuterated methanol isotopologues coming from various existing observational datasets from the IRAM-PdBI and ALMA sub-mm interferometers to estimate the methanol deuteration surrounding three low-mass protostars on Solar System scales. A population diagram analysis allows us to derive a [CH$_2$DOH]/[CH$_3$OH] abundance ratio of 3-6 % and a [CH$_3$OD]/[CH$_3$OH] ratio of 0.4-1.6 % in the warm inner protostellar regions. These values are ten times lower than those derived with previous single-dish observations towards these sources but they are 10-100 times higher than the methanol deuteration measured in massive hot cores. Dust temperature maps obtained from Herschel and Planck observations show that massive hot cores are located in warmer molecular clouds than low-mass sources, with temperature differences of $sim$10 K. Comparison with the predictions of the gas-grain astrochemical model GRAINOBLE shows that such a temperature difference is sufficient to explain the different deuteration observed in low- to high-mass sources, suggesting that the physical conditions of the molecular cloud at the origin of the protostars mostly govern the present observed deuteration of methanol. The methanol deuteration measured in this work is higher by a factor of 5 than the upper limit in methanol deuteration estimated in comet Hale-Bopp, implying that an important reprocessing of the organic material would have occurred in the solar nebula during the formation of the Solar System.
The physical evolution of Young Stellar Objects (YSOs) is accompanied by an enrichment of the molecular complexity, mainly triggered by the heating and energetic processing of the astrophysical ices. In this paper, a study of how the ice column density varies across the protostellar evolution has been performed. Tabulated data of H$_2$O, CO$_2$, CH$_3$OH, HCOOH observed by ground- and space-based telescopes toward 27 early-stage YSOs were taken from the literature. The observational data shows that ice column density and spectral index ($alpha$), used to classify the evolutionary stage, are well correlated. A 2D continuum radiative transfer simulation containing bare and grains covered by ices at different levels of cosmic-ray processing were used to calculate the Spectral Energy Distributions (SEDs) in different angle inclinations between face-on and edge-on configuration. The H$_2$O:CO$_2$ ice mixture was used to address the H$_2$O and CO$_2$ column density variation whereas the CH$_3$OH and HCOOH are a byproduct of the virgin ice after the energetic processing. The simulated spectra were used to calculate the ice column densities of YSOs in an evolutionary sequence. As a result, the models show that the ice column density variation of HCOOH with $alpha$ can be justified by the envelope dissipation and ice energetic processing. On the other hand, the ice column densities are mostly overestimated in the cases of H$_2$O, CO$_2$ and CH$_3$OH, even though the physical and cosmic-ray processing effects are taken into account.
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