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A. Fuente

Publications and source records attributed to A. Fuente.

At least 19 recordsLinked to original sources

Series of core collapse numerical simulations (SOLANUM) I: Modelling the early and late infall in a sun-like protostar

Magnetohydrodynamical simulations and interferometric observations toward young stellar objects reveal the accretion of gas that may alter the physical properties and chemical composition of protostellar disks. Our goal is to constrain the physical history and properties of late infalling gas, and assess its potential to change the physical and chemical properties of the disk. We carried out a core collapse simulation of 5 M$_{\odot}$ of gas endowed with tracer and sink particles during $\sim 3.6\times 10^{5}$ yr. We analyzed the properties of the rotationally supported disk, and the origin and physical history of the gas from which it is initially formed. We also selected the tracer particles that describe the late infall to analyze their origin and physical history, and compare them to the information obtained from the disk. The final mass of the sink reaches 1.02 M$_\odot$, while the mass of the disk stays fairly constant around 0.02 M$_\odot$. Throughout its evolution, the disk radius increases up to $\sim 40$ au and its density is reduced by a factor of $\sim 8$. Filaments that channel gas from the envelope to the disk and sink appear as a result of the magnetic interchange instability. Tracer particles can identify late infalling gas, whose physical properties resemble that of observed streamers and are only accreted in the final snapshots of the simulation. The origin and physical history of the late infalling gas are different from those of the gas that initially forms the disk. Core collapse simulations predict the appearance of filaments that connect the envelope to the disk. The late accretion of gas through these channels has properties similar to those of streamers and brings gas to the disk with a different physical history that could translate into a different chemical composition.

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Discovery of sulfur oxides in the ejecta of a B[e] supergiant

B[e] supergiants represent a rare class of luminous, evolved massive stars surrounded by dusty circumstellar disks. Since their intense UV fields were long thought to sterilize their surroundings, molecular detections beyond carbon monoxide have remained elusive, leaving their chemical reservoirs largely unexplored. Whether these environments can sustain a complex molecular chemistry is a fundamental question with significant astrochemical implications. Here we report the detection of chemically rich molecular gas surrounding the B[e] supergiant HD~87643, using ALMA observations. Our data reveal the presence of the sulfur oxides SO and SO$_2$ and other sulfur-bearing species, marking the first detection of these molecules in an early-type evolved massive star. We find a high fractional abundance of SO$_2$ relative to H$_2$, which our chemical modelling can reproduce in timescales as short as $\sim$10$^4$ yr in an oxygen-rich environment. These results indicate that the detected molecules trace a short-lived, rapidly evolving phase of out-of-equilibrium chemistry. Furthermore, we measure an anomalously low $^{32}$SO/$^{33}$SO, that we attribute to mass-independent fractionation driven by intense photochemistry. This mechanism mirrors processes proposed to explain the $^{33}$S excesses in the atmosphere of the Archaean Earth. Our findings suggest that B[e] supergiants could serve as unique laboratories for studying sulfur chemistry under extreme radiation conditions, opening potential avenues to investigate the fractionation processes that shaped the isotopic signatures found in the early geological record.

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Evolution of Chemistry in the envelope of HOt corinoS (ECHOS). III. Sulphur chemistry in the Class 0 objects HH 212 and NGC 1333 IRAS 4A

Our goal is to find chemical diagnostics to determine the physical conditions in protostellar envelopes and help establish the development of matter during the formation of a low-mass star, as well as investigating a possible variation of sulphur depletion during the star formation process at the scale of the cold envelope. With observations with the Yebes-40m and IRAM-30m telescopes, we estimate column densities of sulphur-bearing species in the Class 0 objects HH212 and NGC1333 IRAS4A. A neural emulator of the chemical code Nautilus is used to constrain the chemical time, density, gas temperature, cosmic ray ionization rate, and sulphur elemental abundance in the cold envelope of these objects. We compare the resulting abundances of these species with those towards the Class 0 object B335. While sulphur-bearing species containing carbon chains are between 3 and 7 times more abundant in B335 than in the other two objects, sulphur oxides and nitrogen-bearing species are 3 times more abundant in NGC1333 IRAS4A. Our chemical modelling shows that, while the chemistry of HH212 and NGC1333 IRAS4A is well reproduced considering a gas temperature of 25 K and a sulphur depletion of a factor of 100 in their envelopes, significant differences are found in their average density and cosmic ray ionization rate. Comparing with similar studies in pre-stellar and protostellar cores, we derive an increase in the SO/CS and SO$_2$/C$_2$S ratios of about two orders of magnitude and a potential decrease in the HCS$^+$/CS ratio of a factor of 10 in the transition from the pre-stellar to the Class 0 phase. Sulphur compounds are good evolutionary tracers of the pre- to protostellar phase transition, with oxygen-bearing species being more abundant than those containing carbon in the evolved sources. Nonetheless, sulphur depletion in the cold envelope of Class 0 objects remains similar to that in starless cores.

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Modeling the UV-photon irradiation of CS$_2$-bearing ices in the laboratory with the pyRate gas-grain astrochemical code. New insights into the missing sulfur problem

Observations indicate that the total abundance of S-bearing species in dense clouds is orders of magnitude lower than the cosmic sulfur abundance. Addressing this "missing sulfur problem" requires a combination of astronomical observations, laboratory experiments, and theoretical models. In this work, we use the pyRate astrochemical model to simulate the VUV photon irradiation of a CO$_2$:CS$_2$ ice mixture at 10 K in the laboratory, with the goal of supporting the interpretation of the experimental results and testing our current understanding of the sulfur evolution in interstellar ices. For this purpose, the astrochemical model was adapted to the experimental conditions, and the chemical network was compiled from several sources to ensure that all known reactions involving sulfur species were included. The results indicate that nondiffusive chemistry is necessary to reproduce the formation of S-bearing species observed in the experiment. However, some discrepancies were found in the major S-bearing ice chemistry products predicted by the model and the experiment. The compounds OCS, CS, and SO are overpredicted by the model, while it falls short in accounting for $\rm SO_2$ and sulfur allotropes. These discrepancies are likely due to a combination of an incomplete knowledge of the chemical reactions at play (either because of missing reactions and/or because of unconstrained reaction barriers), and uncertainties in the experimental analysis. This work represents the first effort to model the chemistry of a multicomponent ice analog with a rate-equation based code, and highlights the complementary nature of theoretical and experimental astrochemistry to disentangle the chemical evolution of sulfur in the interstellar medium.

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Ice chemistry that can be unveiled with the JWST: SynthIceSpec, a synthetic spectrum generator to test spectral limits. Solid CO_2 as a dust thermometer and solid CH_3CN detectability in cold cores

As the (JWST) pursues its observing journey, several thousands of icy-grain spectra are expected to be measured and analysed. The inventory of ices in particular, via the observations of background sources, is accessible for hundreds of lines of sight (LOSs) per molecular-cloud region, opening the possibility to add strong constraints on the solid phase chemistry in a vast domain of cloud densities. SynthIceSpec is a synthetic infrared (IR) spectrum generator that has been designed as a tool to support observing proposals and to test the outcome of chemical models. It is based on laboratory measurements of pure and mixed ices, where each vibrational component is fitted by a sum of Gaussian profiles. Given an initial ice chemical composition (either set by the user or the outputs of a chemical model), a full JWST spectrum is generated, to which the contribution of silicates; continuum, stellar photospheric absorption bands; and extinction law can be added. For the continuum, stellar photospheric models for a wide range of spectral types can be selected by the program, or, Spectral Energy Distribution (SEDs). We present a few use cases of SynthIceSpec: we probed the impact of dust temperature on CO_2 ice formation using IR data and gas-grain modelling. Next, we used SynthIceSpec to explore the detectability of the main feature of CH_3CN at 4.45 um in a cold core environment with the JWST, which was previously tentatively detected in YSOs. The detection thresholds we derive are reasonably low and observable, but identification is directly impacted by the photosphere absorptions that can greatly hinder identification. For some photostellar types, it could remain feasible. Coupled with the Estimated Time Calculator of the Space Telescope Science Institute, SynthIceSpec can be used to find the optimum observational setup for new observations.

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PRODIGE - envelope to disk with NOEMA: VII. (Complex) organic molecules in the NGC1333 IRAS4B1 outflow: A new laboratory for shock chemistry

Shock chemistry is an excellent tool to shed light on the formation and destruction mechanisms of complex organic molecules (COMs). The L1157-mm outflow is the only low-mass protostellar outflow that has extensively been studied in this regard. Using the data taken as part of the PRODIGE (PROtostars & DIsks: Global Evolution) large program, we aim to map COM emission and derive the molecular composition of the protostellar outflow driven by the Class 0 protostar NGC1333 IRAS4B1 to introduce it as a new laboratory to study the impact of shocks on COM chemistry. In addition to typical outflow tracers such as SiO and CO, outflow emission is seen from H2CO, HNCO, and HC3N, as well as from the COMs CH3OH, CH3CN, and CH3CHO, and even from deuterated species such as DCN, D2CO, and CH2DOH. Maps of integrated intensity ratios between CH3OH and DCN, D2CO, and CH3CHO reveal gradients with distance from the protostar. Intensity ratio maps of HC3N and CH3CN with respect to CH3OH peak in the southern lobe where temperatures are highest. Rotational temperatures derived towards two positions, one in each lobe, are found in the range ~50-100 K. Abundances with respect to CH3OH are higher by factors of a few than for the L1157-B1. In conclusion, for the first time, we securely detected the COMs CH3CN, CH3CHO, and CH2DOH in the IRAS 4B1 outflow, serendipitously with limited sensitivity and bandwidth. Targeted observations will enable the discovery of new COMs and a more detailed analysis of their emission. Morphological differences between molecules in the IRAS 4B1 outflow lobes and their relative abundances provide first proof that this outflow is a promising new laboratory for shock chemistry, which will offer crucial information on COM formation and destruction as well as outflow structure and kinematics.

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PDRs4All XVIII. JWST-NIRCam Photometric properties of protoplanetary disks in the Orion Nebula Cluster

We use the high angular resolution NIRCam images from the PDRs4All program, combined with those of GTO program 1256, to extract key properties of disks in the Orion Nebula Cluster. We measure disk radii in silhouette against the bright background, identify dissociation fronts (DFs) and ionization fronts (IFs), determine Paschen $\alpha$ intensities, and derive near-infrared spectral energy distributions (SEDs). From these diagnostics we define a typology of ONC disks. Type I sources show merged IFs and DFs close to the disk surface. Type II sources have DFs at the disk surface and IFs located tens of astronomical units away. Type III sources show a DF at the disk surface but no IF. For all types, PAH emission traces the PDR. We find that the disk radius $r_{\rm disk}$ increases with projected distance to the ionizing source $d_{\rm proj}$, following $r_{\rm disk} \propto d_{\rm proj}^{0.30}$, consistent with disk truncation by photoevaporation. Disk radii measured in the infrared are larger than those measured at millimeter wavelengths, suggesting radial dust segregation within the disks. In agreement with PDR models, the thermal pressure in the disk PDR increases with the FUV radiation field $G_0$, but with a flatter slope. Finally, the SEDs of candidate Jupiter Mass Binary Objects (JuMBOs) are similar to those of Type III disks, except for JuMBO24, which resembles a Type I or Type II source. Its SED is consistent with a young low-mass binary hosting an unresolved ionized disk.

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Chemical study of two starless cores in the B213/L1495 filament

The chemical evolution of pre-stellar cores during their transition to a protostellar stage is not yet fully understood. Detailed chemical characterizations of these sources are needed to better define their chemistry during star formation. Our goal is to characterize the chemistry of the starless cores C2 and C16 in the B213/L1495 filament of the Taurus Molecular Cloud, and to understand how it relates to the environmental conditions and the evolutionary state of the cores. We made use of two complete spectral surveys at 7 mm of these sources, carried out using the Yebes 40-m telescope. Derived molecular abundances were compared with those of other sources in different evolutionary stages and with values computed by chemical models. Including isotopologs, 22 molecules were detected in B213-C2, and 25 in B213-C16. The derived rotational temperatures have values of between $\sim$ 5 K and $\sim$ 9 K. A comparison of the two sources shows lower abundances in C2, except for l-C$_{3}$H and HOCO$^{+}$, which have similar values in both cores. Model results indicate that both cores are best fit assuming early-time chemistry, and point to C2 being in a more advanced evolutionary stage, as it presents a higher molecular hydrogen density and sulfur depletion, and a lower cosmic-ray ionization rate. Our chemical modeling successfully accounts for the abundances of most molecules, including complex organic molecules and long cyanopolynes (HC$_{5}$N, HC$_{7}$N), but fails to reproduce those of the carbon chains CCS and C$_{3}$O. Chemical differences between C2 and C16 could stem from the evolutionary stage of the cores, with C2 being closer to the pre-stellar phase. Both cores are better fit assuming early-time chemistry of t $\sim$ 0.1 Myr. The more intense UV radiation in the northern region of B213 could account for the high abundances of l-C$_{3}$H and HOCO$^{+}$ in C2.

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Why the Northern Hemisphere Needs a 30-40 m Telescope and the Science at Stake. How do Planetary Systems Form?

The detection and characterization of protoplanets in protoplanetary disks around young stars is emerging as a transformative field that will redefine our understanding of how planetary systems form. While current facilities have revealed the diversity of mature exoplanets and the complex structures of disks, we still lack the crucial observational link between them: a statistically meaningful census of planets caught in the act of formation. This white paper argues that such a breakthrough requires access to the nearest and most informative star-forming regions, roughly half of which are poorly accessible or entirely unreachable from Cerro Armazones. Although the ELT alone will strongly impact our knowledge of planet formation, its location prevents Europe from fully exploiting the necessary parameter space. A 30-40 m telescope in the northern hemisphere is therefore essential for obtaining diffraction-limited imaging of protoplanets and disks across the entire sky, enabling robust demographics, exploiting synergies with ngVLA, Gaia, and other facilities covering the north, and ensuring that Europe remains at the forefront of the planet-formation revolution in the coming decades.

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Observations of sulfuretted species in HL Tau

Protoplanetary disks inherit their chemical composition from their natal molecular cloud, but the extent to which this material is preserved versus reset through chemical reprocessing remains an open question. Understanding this balance is a major topic in astrochemistry. Comparing the chemical composition of the envelope and the protoplanetary disk is key to solving the topic. The goal of this paper is to investigate the chemical differences between the disk and the surrounding envelope by comparing the column density ratios of a few selected species in each region. The source we focus on is HL Tau. We present new NOEMA observations of HL Tau targeting the following species: CS, H2CO, H2S, and SO2. We produced zeroth-, first-, and second-moment maps for the species where emission was detected and used them to analyze the spatial distribution and kinematic properties of the different molecules in the disk and the envelope. We derived the column densities and compared the values derived for the envelope and disk. We also computed the rotational diagram for the SO2 detected transitions. Assuming two different temperature regimes, 17 and 58 K, we derived column densities for the species surveyed in the disk and compared them with values derived for the envelope. We find large differences in the derived column density ratios of the surveyed molecules, especially for N(CS)/N(H2S), which is 40 to 50 times larger in the envelope. We attribute these variations to the different excitation and UV-irradiation regimes in the disk and envelope. We also note strong gradients in the ratios between different positions of the disk and tentatively attribute them to different levels of turbulence at different azimuths. The observed differences in molecular ratios in the envelope and the disk are suggestive of chemical reprocessing of the gas during the formation and evolution of the protoplanetary disk.

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A quest for sulfur-bearing refractory species. Identification of CaS in the interstellar medium

The recent detection of refractory molecules in massive star-forming regions provides a means of probing the innermost regions of disks around massive stars. These detections also make it possible to explore the chemical composition of refractories through gas-phase observations. In this regard, identifying refractory compounds containing sulfur could reveal potential connections between sulfur and refractories, as well as help determine the sulfur budget in these extreme environments. We find convincing evidence of a reliable detection of CaS, and tentative detections of KS and KSH in the disk G351.77-mm1. These are the first ever identifications of these species in the interstellar medium. The CaS, KS, and KSH column densities are about 3 orders of magnitude lower than those of the abundant sulfur compounds SO$_2$, CH$_3$SH and SiS, proving that these species are not the major reservoir of sulfur at the spatial scales probed by our observations. Higher angular resolution observations at different wavelengths are required to confirm these detections, which are of paramount importance to gain insights into the formation of gas-phase refractory molecules.

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Fine-tuning the complex organic molecule formation: sulfur and CO ice as regulators of surface chemistry

Grain-surface chemistry plays a crucial role in the formation of molecules of astrobiological interest, including H$_{2}$S and complex organic molecules (COMs). They are commonly observed in the gas phase toward star-forming regions, but their detection in ices remains limited. Combining gas-phase observations with chemical modeling is therefore essential for advancing our understanding of their chemistry. In this paper we investigate the factors that promote or hinder molecular complexity combining gas-phase observations of CH$_{3}$OH, H$_{2}$S, OCS, N$_{2}$H$^{+}$, and C$^{18}$O with chemical modeling in two dense cores: Barnard-1b and IC348. We observed millimeter emission lines of CH$_{3}$OH, H$_{2}$S, OCS, N$_{2}$H$^{+}$, and C$^{18}$O along strips using the IRAM 30m and Yebes 40m telescopes. We used the gas-grain chemical model \texttt{Nautilus} to reproduce the observed abundance profiles adjusting parameters such as initial sulfur abundances and binding energies. H$_{2}$S, N$_{2}$H$^{+}$ and C$^{18}$O gas-phase abundances vary up to one order of magnitude towards the extinction peak. CH$_{3}$OH abundance remains quite uniform. These abundances can only be reproduced assuming a decreasing sulfur budget, which lowers H$_{2}$S and enhances CH$_{3}$OH abundances. Decreasing binding energies, which are expected in CO-rich apolar ices, are also required. The sulfur depletion required by H$_2$S is generally higher than that required by CH$_3$OH, suggesting unknown sulfur sinks. These findings highlight the intricate relationship between sulfur chemistry and COM formation, driven by the competition between sulfur and CO for hydrogen atoms. Our study emphasizes that the growth of CO ice and the progressive sequestration of hydrogen atoms by sulfur are critical in determining whether chemical complexity can develop, providing key insights into the early stages of star and planet formation.

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ANTIHEROES-PRODIGE: Quantifying the connection from envelope to disk with the IRAM 30m telescope and NOEMA I. Attack of the streamers: L1448N's fight for order in the chaos

Star formation is a hierarchical process ranging from molecular clouds down to individual protostars. In particular how infalling asymmetric structures, called streamers, delivering new material onto protostellar systems, are connected to the surrounding envelope is not understood. We investigate the connection between the cloud material at 10000 au scales down to 300 au scales towards L1448N in the Perseus star-forming region hosting three young Class 0/I protostellar systems. Sensitive molecular line observations taken with the IRAM 30m telescope and NOEMA at 1.4 mm are used to study the kinematic properties in the region traced by the molecular lines. Several infalling streamers are associated with the protostellar systems, some of them traced by C18O and DCN, while one of them is bright in SO and SO2. The kinematic properties of the former streamers are consistent with the velocities observed at large envelope scales of 10000 au, while the latter case show different kinematics. The masses and infall rates of the streamers are 0.01 Msun and 0.01-0.1 Msun and 10^-6 Msun/yr and 5-18x10^-6 Msun/yr for IRS3A and IRS3C, respectively. The envelope mass in the L1448N region is ~16Msun, thus the mass of a single streamer is low compared to the envelope mass (<1%). However, compared to the estimated mass of the protostellar systems a single streamer could deliver up to 1% and 8-17% of mass towards IRS3A (M*~1.2 Msun) and IRS3C (M*~1 Msun), respectively. The rotational signatures of structures in L1448N are all connected - from the large-scale envelope, infalling streamers, down to the rotation of all three disks. Two of the three Class 0/I protostellar systems are still fed by this surrounding material, which can be associated to the remnant envelope. However, we also find a streamer that is bright in SO and SO2 towards IRS3C that could be connected to a nearby sulfur reservoir.

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Gas-phase Elemental abundances in Molecular cloudS (GEMS) XI. The evolution of HCN, HNC, and N2H+ isotopic ratios in starless cores

Isotopic ratios have been used as chemical diagnostics to investigate the origin of the material in the Solar System. We have determined the HCN, HNC, and N2H+ isotopic ratios and the chemical age in a large sample of 23 starless cores located in different environments. This work uses IRAM 30m data to constrain the D/H ratio of HCN, HNC, and N2H+ as well as the 14N/15N ratio of HCN and HNC. The observed abundances have been modeled using the chemical code DNAUTILUS 2.0. Deuterated compounds are detected in all of our sample cores, with average DNC/HNC, DCN/HCN, and N2D+/N2H+ values of 0.054$\pm$0.019, 0.036$\pm$0.033, and 0.15$\pm$0.11, respectively. The deuterium fractions (Dfrac) show a weak correlation with temperature and a large scatter that reflects that other factors such as core evolution could also play a significant role. Our chemical model is able to reproduce all the observed values with 0.2-0.3 Myr in Taurus and 0.3-0.5 Myr in Perseus and Orion. The 14N/15N isotopic ratio is found to be different between HCN/HC15N (430$\pm$120) and HNC/H15NC (296$\pm$64). We find no correlation between these ratios and the deuterium fractions, but we report a weak correlation with temperature. The Dfrac of HCN, HNC, and N2H+ can be used as evolutionary tracers of starless cores as long as the physical parameters are well constrained. The HCN/HC15N and HNC/H15NC ratios are not correlated with Dfrac, suggesting that the detected variations are not correlated with the core evolutionary stage. The average value of the HCN/HC15N ratio in our sample is significantly higher than the values measured in protostars and protoplanetary disks, possibly indicating that nitrogen fractionation processes are taking place during the protostellar phase.

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PRODIGE VI -- Envelope to Disk with NOEMA: VI. The Missing Sulfur Problem

Determining the amount of sulfur in volatiles and refractories in the ISM remains one of the main problems in astrochemistry. The detection of H$_2$S ices, which are thought to be one of the main sulfur reservoirs, has not been achieved yet, and the only S-bearing species detected in the ices to date is OCS. PRODIGE large survey observations with NOEMA of several Class 0/I protostars in the Perseus Molecular Cloud provide a perfect opportunity to study the H$_2$S and OCS composition of the ices through the volatiles sublimated in the warm inner core (T$>$100K, n $\sim10^6$cm$^{-3}$) of these protostars. Our aim is to determine the H$_2$S/OCS ratio in the warm inner core of 24 protostars in order to study how it is affected by different factors during its evolution. We used the NOEMA millimeter observations from the PRODIGE program of H$_2$S, H$_2^{33}$S, OCS, OC$^{33}$S and OC$^{34}$S to estimate the H$_2$S and OCS column densities in the warm inner cores. We used SO and SO$_2$ data from the ALMA archive to give a rough estimate of the total sulfur abundance. We explore the chemistry of H$_2$S and OCS in the warm cores using chemical and dynamical simulations of the collapse of a dense core to form a protostar. The estimated H$_2$S/OCS ratio reveals a segregation of the sources into ``OCS-poor'' and ``OCS-rich'' protostars, where the OCS-poor protostars present higher H$_2$S/OCS ratios than the OCS-rich ones. Total sulfur abundance is always dominated by either H$_2$S or OCS, grows with evolution during the Class 0 phase up to $D_S<8$, and decreases again in the Class I. Simulations show that temperature changes in the pre-stellar phase and during the collapse can produce substantial differences in the H$_2$S and OCS abundances and in the H$_2$S/OCS ratio. Our analysis shows that the H$_2$S/OCS ratio is strongly influenced by the environment and the initial conditions of the cloud.

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PDRs4All XV: CH radical and H$_3^+$ molecular ion in the irradiated protoplanetary disk d203-506

Most protoplanetary disks experience a phase in which they are subjected to strong ultraviolet radiation from nearby massive stars. This UV radiation can substantially alter their chemistry by producing numerous radicals and molecular ions. In this Letter we present detailed analysis of the JWST-NIRSpec spectrum of the d203-506 obtained as part of the PDRs4All Early Release Science program. Using state-of-the-art spectroscopic data, we searched for species using a multi-molecule fitting tool, PAHTATmol, that we developed for this purpose. Based on this analysis, we report the clear detection of ro-vibrational emission of the CH radical and likely detection of the H$_3^+$ molecular ion, with estimated abundances of a few times 10$^{-7}$ and approximately 10$^{-8}$, respectively. The presence of CH is predicted by gas-phase models and well explained by hydrocarbon photochemistry. H$_3^+$ is usually formed through reactions of H$_2$ with H$_2^+$ originating from cosmic ray ionization of H$_2$. However, recent theoretical studies suggest that H$_3^+$ also forms through UV-driven chemistry in strongly irradiated ($G_0>$10$^3$), dense ($n_{\rm H} >10^{6}$ cm$^{-3}$) gas. The latter is favored as an explanation for the presence of ``hot'' H$_3^+$ ($T_{\rm ex}\gtrsim$1000 K) in the outer disk layers of d203-506, coinciding with the emission of FUV-pumped H$_2$ and other ``PDR species'', such as CH$^+$, CH$_3^+$, and OH. Our detection of infrared emission from vibrationally excited H$_3^+$ and CH raises questions about their excitation mechanisms and, underscore that UV radiation can have a profound impact on the chemistry of planet forming disks. They also demonstrate the power of JWST pushing the limit for the detection of elusive species in protoplanetary disks.

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PRODIGE - envelope to disk with NOEMA: V. Low 12C/13C ratios for CH3OH and CH3CN in hot corinos

The 12C/13C isotope ratio has been derived towards numerous cold clouds (20-50 K) and a couple protoplanetary disks and exoplanet atmospheres. However, direct measurements of this ratio in the warm gas (>100 K) around young low-mass protostars remain scarce, but are required to study its evolution during star and planet formation. We derived 12C/13C ratios from the isotopologues of the complex organic molecules (COMs) CH3OH and CH3CN in the warm gas towards seven Class 0/I protostellar systems to improve our understanding of the evolution of the 12C/13C ratios during star and planet formation. We used the data that were taken as part of the PRODIGE large program with the NOEMA at 1mm. The emission of CH3OH and CH3CN is spatially unresolved in the PRODIGE data (300au scale). Derived rotational temperatures exceed 100K, telling us that they trace the gas of the hot corino, where CH3CN probes hotter regions than CH3OH on average (290 K versus 180 K). The column density ratios between the 12C and 13C isotopologues, derived from LTE analysis, range from 4 to 30, thus, are significantly lower than the expected local ISM isotope ratio of about 68. Assuming that CH3CN and CH3OH may inherit the 12C/13C ratio from their precursor species, astrochemical models were conducted for the latter and compared with our observational results. We conclude that an enrichment in 13C in COMs at the earliest protostellar stages is likely inherited from the COMs' precursor species, whose 12C/13C ratios are set during the prestellar stage via isotopic exchange reactions. This also implies that low 12C/13C ratios observed at later evolutionary stages could at least partially be inherited. A final conclusion on 12C/13C ratios in protostellar environments requires improved observations to tackle current observational limitations and additional modelling efforts.

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PDRs4All. XII. FUV-driven formation of hydrocarbon radicals and their relation with PAHs

We present subarcsecond-resolution ALMA mosaics of the Orion Bar PDR in [CI] 609um, C2H (4-3), and C18O (3-2) emission lines complemented by JWST images of H2 and aromatic infrared band (AIB) emission. The rim of the Bar shows very corrugated structures made of small-scale H2 dissociation fronts (DFs). The [CI] 609 um emission peaks very close (~0.002 pc) to the main H2-emitting DFs, suggesting the presence of gas density gradients. These DFs are also bright and remarkably similar in C2H emission, which traces "hydrocarbon radical peaks" characterized by very high C2H abundances, reaching up to several x10^-7. The high abundance of C2H and of related hydrocarbon radicals, such as CH3, CH2, and CH, can be attributed to gas-phase reactions driven by elevated temperatures, the presence of C+ and C, and the reactivity of FUV-pumped H2. The hydrocarbon radical peaks roughly coincide with maxima of the 3.4/3.3 um AIB intensity ratio, a proxy for the aliphatic-to-aromatic content of PAHs. This implies that the conditions triggering the formation of simple hydrocarbons also favor the formation (and survival) of PAHs with aliphatic side groups, potentially via the contribution of bottom-up processes in which abundant hydrocarbon radicals react in situ with PAHs. Ahead of the DFs, in the atomic PDR zone (where [H]>>[H2]), the AIB emission is the brightest, but small PAHs and carbonaceous grains undergo photo-processing due to the stronger FUV field. Our detection of trace amounts of C2H in this zone may result from the photoerosion of these species. This study provides a spatially resolved view of the chemical stratification of key carbon carriers in a PDR. Overall, both bottom-up and top-down processes appear to link simple hydrocarbon molecules with PAHs in molecular clouds; however, the exact chemical pathways and their relative contributions remain to be quantified.

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