arXiv subjects

Ewine F. van Dishoeck

Publications and source records attributed to Ewine F. van Dishoeck.

At least 199 records · Page 11Linked to original sources

arXiv2015

Double DCO+ rings reveal CO ice desorption in the outer disk around IM Lup

In a protoplanetary disk, a combination of thermal and non-thermal desorption processes regulate where volatiles are liberated from icy grain mantles into the gas phase. Non-thermal desorption should result in volatile-enriched gas in disk-regions where complete freeze-out is otherwise expected. We present ALMA observations of the disk around the young star IM Lup in 1.4 mm continuum, C18O 2-1, H13CO+ 3-2 and DCO+ 3-2 emission at ~0".5 resolution. The images of these dust and gas tracers are clearly resolved. The DCO+ line exhibits a striking pair of concentric rings of emission that peak at radii of ~0".6 and 2" (~90 and 300 AU, respectively). Based on disk chemistry model comparison, the inner DCO+ ring is associated with the balance of CO freeze-out and thermal desorption due to a radial decrease in disk temperature. The outer DCO+ ring is explained by non-thermal desorption of CO ice in the low-column-density outer disk, repopulating the disk midplane with cold CO gas. The CO gas then reacts with abundant H2D+ to form the observed DCO+ outer ring. These observations demonstrate that spatially resolved DCO+ emission can be used to trace otherwise hidden cold gas reservoirs in the outmost disk regions, opening a new window onto their chemistry and kinematics.

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arXiv2015

A low-mass protostar's disk-envelope interface: disk-shadowing evidence from ALMA DCO+ observations of VLA1623

Due to instrumental limitations and a lack of disk detections, the structure between the envelope and the rotationally supported disk has been poorly studied. This is now possible with ALMA through observations of CO isotopologs and tracers of freezeout. Class 0 sources are ideal for such studies given their almost intact envelope and young disk. The structure of the disk-envelope interface of the prototypical Class 0 source, VLA1623A which has a confirmed Keplerian disk, is constrained from ALMA observations of DCO+ 3-2 and C18O 2-1. The physical structure of VLA1623 is obtained from the large-scale SED and continuum radiative transfer. An analytic model using a simple network coupled with radial density and temperature profiles is used as input for a 2D line radiative transfer calculation for comparison with the ALMA Cycle 0 12m array and Cycle 2 ACA observations of VLA1623. DCO+ emission shows a clumpy structure bordering VLA1623A's Keplerian disk, suggesting a cold ring-like structure at the disk-envelope interface. The radial position of the observed DCO+ peak is reproduced in our model only if the region's temperature is between 11-16K, lower than expected from models constrained by continuum and SED. Altering the density has little effect on the DCO+ position, but increased density is needed to reproduce the disk traced in C18O. The DCO+ emission around VLA1623A is the product of shadowing of the envelope by the disk. Disk-shadowing causes a drop in the gas temperature outside of the disk on >200AU scales, encouraging deuterated molecule production. This indicates that the physical structure of the disk-envelope interface differs from the rest of the envelope, highlighting the drastic impact that the disk has on the envelope and temperature structure. The results presented here show that DCO+ is an excellent cold temperature tracer.

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arXiv2015

The complex chemistry of outflow cavity walls exposed: the case of low-mass protostars

Complex organic molecules are ubiquitous companions of young low-mass protostars. Recent observations suggest that their emission stems, not only from the traditional hot corino, but also from offset positions. In this work, 2D physicochemical modelling of an envelope-cavity system is carried out. Wavelength-dependent radiative transfer calculations are performed and a comprehensive gas-grain chemical network is used to simulate the physical and chemical structure. The morphology of the system delineates three distinct regions: the cavity wall layer with time-dependent and species-variant enhancements; a torus rich in complex organic ices, but not reflected in gas-phase abundances; and the remaining outer envelope abundant in simpler solid and gaseous molecules. Strongly irradiated regions, such as the cavity wall layer, are subject to frequent photodissociation in the solid phase. Subsequent recombination of the photoproducts leads to frequent reactive desorption, causing gas-phase enhancements of several orders of magnitude. This mechanism remains to be quantified with laboratory experiments. Direct photodesorption is found to be relatively inefficient. If radicals are not produced directly in the icy mantle, the formation of complex organics is impeded. For efficiency, a sufficient number of FUV photons needs to penetrate the envelope; and elevated cool dust temperatures need to enable grain-surface radical mobility. As a result, a high stellar luminosity and a sufficiently wide cavity favor chemical complexity. Furthermore within this paradigm, complex organics are demonstrated to have unique lifetimes and be grouped into early (formaldehyde, ketene, methanol, formic acid, methyl formate, acetic acid, glycolaldehyde) and late (acetaldehyde, dimethyl ether, ethanol) species.

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arXiv2015

Photodesorption of H2O, HDO, and D2O ice and its impact on fractionation

The HDO/H2O ratio in interstellar gas is often used to draw conclusions on the origin of water in star-forming regions and on Earth. In cold cores and in the outer regions of protoplanetary disks, gas-phase water comes from photodesorption of water ice. We present fitting formulae for implementation in astrochemical models using photodesorption efficiencies for all water ice isotopologues obtained using classical molecular dynamics simulations. We investigate if the gas-phase HDO/H2O ratio reflects that present in the ice or whether fractionation can occur during photodesorption. Probabilities for the top four monolayers are presented for photodesorption of X (X=H,D) atoms, OX radicals, and X2O and HDO molecules following photodissociation of H2O, D2O, and HDO in H2O amorphous ice at temperatures from 10-100 K. Isotope effects are found for all products: (1) H atom photodesorption probabilities from H2O ice are larger than those for D atom photodesorption from D2O ice by a factor of 1.1; the ratio of H and D photodesorbed upon HDO photodissociation is a factor of 2. This process will enrich the ice in deuterium atoms over time; (2) the OD/OH photodesorption ratio upon D2O and H2O photodissociation is on average a factor of 2, but the ratio upon HDO photodissociation is almost constant at unity for all temperatures; (3) D atoms are more effective in kicking out neighbouring water molecules than H atoms. However, the ratio of the photodesorbed HDO and H2O molecules is equal to the HDO/H2O ratio in the ice, therefore, there is no isotope fractionation upon HDO and H2O photodesorption. Nevertheless, the enrichment of the ice in D atoms due to photodesorption can over time lead to an enhanced HDO/H2O ratio in the ice, and, when photodesorbed, also in the gas. The extent to which the ortho/para ratio of H2O can be modified by the photodesorption process is also discussed. (Abridged)

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arXiv2015

Molecular photodissociation

Photodissociation is the dominant removal process of molecules in any region exposed to intense ultraviolet (UV) radiation. This includes diffuse and translucent interstellar clouds, dense photon-dominated regions, high velocity shocks, the surface layers of protoplanetary disks, and cometary and exoplanetary atmospheres. The rate of photodissociation depends on the cross sections for absorption into a range of excited electronic states, as well as on the intensity and shape of the radiation field at each position into the region of interest. Thus, an acccurate determination of the photodissociation rate of even a simple molecule like water or carbon monoxide involves many detailed considerations ranging from its electronic structure to its dissociation dynamics and the specifics of the radiation field that the molecule is exposed to. In this review chapter, each of these steps in determining photodissociation rates is discussed systematically and examples are provided.

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arXiv2015

APEX-CHAMP+ high-J CO observations of low-mass young stellar objects: IV. Mechanical and radiative feedback

During the embedded stage of star formation, bipolar molecular outflows and UV radiation from the protostar are important feedback processes. Our aim is to quantify the feedback, mechanical and radiative, for a large sample of low-mass sources. The outflow activity is compared to radiative feedback in the form of UV heating by the accreting protostar to search for correlations and evolutionary trends. Large-scale maps of 26 young stellar objects, which are part of the Herschel WISH key program are obtained using the CHAMP+ instrument on the APEX (12CO and 13CO 6-5), and the HARP-B instrument on the JCMT (12CO and 13CO 3-2). Maps are used to determine outflow parameters and envelope models are used to quantify the amount of UV-heated gas and its temperature from 13CO 6-5 observations. All sources in our sample show outflow activity and the outflow force, F_CO, is larger for Class 0 sources than for Class I sources, even if their luminosities are comparable. The outflowing gas typically extends to much greater distances than the power-law envelope and therefore influences the surrounding cloud material directly. Comparison of the CO 6-5 results with Herschel-HIFI H2O and PACS high-J CO lines, both tracing currently shocked gas, shows that the two components are linked, even though the transitions do not probe the same gas. The link does not extend down to CO 3-2. The conclusion is that CO 6-5 depends on the shock characteristics (density and velocity), whereas CO 3-2 is more sensitive to conditions in the surrounding environment (density). The radiative feedback is responsible for increasing the gas temperature by a factor of two, up to 30-50 K, on scales of a few thousand AU, particularly along the direction of the outflow. The mass of the UV heated gas exceeds the mass contained in the entrained outflow in the inner ~3000 AU and is therefore at least as important on small scales.

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arXiv2015

Complex organic molecules in organic-poor massive young stellar objects

Massive young stellar objects (MYSOs) with hot cores are classic sources of complex organic molecules. The origins of these molecules in such sources, as well as the small- and large-scale differentiation between nitrogen- and oxygen-bearing complex species, are poorly understood. We aim to use complex molecule abundances toward a chemically less explored class of MYSOs with weak hot organic emission lines to constrain the impact of hot molecular cores and initial ice conditions on the chemical composition toward MYSOs. We use the IRAM 30m and the Submillimeter Array to search for complex organic molecules over 8-16 GHz in the 1~mm atmospheric window toward three MYSOs with known ice abundances, but without luminous molecular hot cores. Complex molecules are detected toward all three sources at comparable abundances with respect to CH$_3$OH to classical hot core sources. The relative importance of CH$_3$CHO, CH$_3$CCH, CH$_3$OCH$_3$, CH$_3$CN, and HNCO differ between the organic-poor MYSOs and hot cores, however. Furthermore, the N-bearing molecules are generally concentrated toward the source centers, while most O- and C-bearing molecules are present both in the center and in the colder envelope. Gas-phase HNCO/CH$_3$OH ratios are tentatively correlated with the ratios of NH$_3$ ice over CH$_3$OH ice in the same lines of sight, which is consistent with new gas-grain model predictions. Hot cores are not required to form complex organic molecules, and source temperature and initial ice composition both seem to affect complex organic distributions toward MYSOs. To quantify the relative impact of temperature and initial conditions requires, however, a larger spatially resolved survey of MYSOs with ice detections.

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arXiv2014

Ro-vibrational excitation of an organic molecule (HCN) in protoplanetary disks

(Abridged) Organic molecules are important constituents of protoplanetary disks. Their ro-vibrational lines observed in the near- and mid-infrared are commonly detected toward T Tauri disks. These lines are the only way to probe the chemistry in the inner few au where terrestrial planets form. To understand this chemistry, accurate molecular abundances have to be determined. This is complicated by excitation effects. Most analyses so far have made the assumption of local thermal equilibrium (LTE). Starting from estimates for the collisional rate coefficients of HCN, non-LTE slab models of the HCN emission were calculated to study the importance of different excitation mechanisms. Using a new radiative transfer model, the HCN emission from a full two-dimensional disk was then modeled to study the effect of the non-LTE excitation, together with the line formation. We ran models tailored to the T Tauri disk AS 205 (N) where HCN lines in both the 3 μm and 14 μm bands have been observed by VLT-CRIRES and the Spitzer Space Telescope. Reproducing the observed 3 μm / 14 μm flux ratios requires very high densities and kinetic temperatures ($n > 10^{14}$ cm$^{-3}$ and $T > 750$ K), if only collisional excitation is accounted for. Radiative pumping can, however, excite the lines easily out to considerable radii $\sim$ 10 au. Consequently, abundances derived from LTE and non-LTE models do not differ by more than a factor of about 3. Models with both a strongly enhanced abundance within $\sim$ 1 au (jump abundance) and constant abundance can reproduce the current observations, but future observations with the MIRI instrument on JWST and METIS on the E-ELT can easily distinguish between the scenarios and test chemical models. Depending on the scenario, ALMA can detect rotational lines within vibrationally excited levels.

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arXiv2014

Astrochemistry of dust, ice and gas: introduction and overview

A brief introduction and overview of the astrochemistry of dust, ice and gas and their interplay is presented, aimed at non-specialists. The importance of basic chemical physics studies of critical reactions is illustrated through a number of recent examples. Such studies have also triggered new insight into chemistry, illustrating how astronomy and chemistry can enhance each other. Much of the chemistry in star- and planet-forming regions is now thought to be driven by gas-grain chemistry rather than pure gas-phase chemistry, and a critical discussion of the state of such models is given. Recent developments in studies of diffuse clouds and PDRs, cold dense clouds, hot cores, protoplanetary disks and exoplanetary atmospheres are summarized, both for simple and more complex molecules, with links to papers presented in this volume. In spite of many lingering uncertainties, the future of astrochemistry is bright: new observational facilities promise major advances in our understanding of the journey of gas, ice and dust from clouds to planets.

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arXiv2014

Herschel/PACS view of disks around low-mass stars and brown dwarfs in the TW Hya association

We conducted Herschel/PACS observations of five very low-mass stars or brown dwarfs located in the TW Hya association with the goal of characterizing the properties of disks in the low stellar mass regime. We detected all five targets at $70\,μ{\rm{m}}$ and $100\,μ{\rm{m}}$ and three targets at $160\,μ{\rm{m}}$. Our observations, combined with previous photometry from 2MASS, WISE, and SCUBA-2, enabled us to construct SEDs with extended wavelength coverage. Using sophisticated radiative transfer models, we analyzed the observed SEDs of the five detected objects with a hybrid fitting strategy that combines the model grids and the simulated annealing algorithm and evaluated the constraints on the disk properties via the Bayesian inference method. The modelling suggests that disks around low-mass stars and brown dwarfs are generally flatter than their higher mass counterparts, but the range of disk mass extends to well below the value found in T Tauri stars, and the disk scale heights are comparable in both groups. The inferred disk properties (i.e., disk mass, flaring, and scale height) in the low stellar mass regime are consistent with previous findings from large samples of brown dwarfs and very low-mass stars. We discuss the dependence of disk properties on their host stellar parameters and find a significant correlation between the Herschel far-IR fluxes and the stellar effective temperatures, probably indicating that the scaling between the stellar and disk masses (i.e., $M_{\rm{disk}} \propto M_{\star}$) observed mainly in low-mass stars may extend down to the brown dwarf regime.

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arXiv2014

A Substellar-Mass Protostar and its Outflow of IRAS 15398-3359 Revealed by Subarcsecond-Resolution Observations of H$_2$CO and CCH

Sub-arcsecond ($0.^{\prime\prime}5$) images of H$_2$CO and CCH line emission have been obtained in the $0.8$ mm band toward the low-mass protostar IRAS 15398-3359 in the Lupus 1 cloud as one of the Cycle 0 projects of the Atacama Large Millimeter/Submillimeter Array. We have detected a compact component concentrated in the vicinity of the protostar and a well-collimated outflow cavity extending along the northeast-southwest axis. The inclination angle of the outflow is found to be about $20^\circ$, or almost edge-on, based on the kinematic structure of the outflow cavity. This is in contrast to previous suggestions of a more pole-on geometry. The centrally concentrated component is interpreted by use of a model of the infalling rotating envelope with the estimated inclination angle, and the mass of the protostar is estimated to be less than $0.09\ M_\odot$. Higher spatial resolution data are needed to infer the presence of a rotationally supported disk for this source, hinted at by a weak high-velocity H$_2$CO emission associated with the protostar.

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arXiv2014

Protoplanetary disk masses from CO isotopologues line emission

One of the methods for deriving disk masses relies on direct observations of the gas, whose bulk mass is in the outer cold ($T\lesssim30$K) regions. This zone can be well traced by rotational lines of less abundant CO isotopologues, that probe the gas down to the midplane. The total CO gas mass is then obtained with the isotopologue ratios taken to be constant at the elemental isotope values found in the local ISM. This approach is however imprecise, because isotope selective processes are ignored. The aim of this work is an isotopologue selective treatment of CO isotopologues, in order to obtain a more accurate determination of disk masses. The isotope-selective photodissociation, the main process controlling the abundances of CO isotopologues in the CO-emissive layer, is properly treated for the first time in a full disk model (DALI, Bruderer et al. 2012; Bruderer 2013). The chemistry, thermal balance, line and continuum radiative transfer are all considered together with a chemical network that treats $^{13}$CO, C$^{18}$O, C$^{17}$O, isotopes of all included atoms, and molecules, as independent species. Isotope selective processes lead to regions in the disk where the isotopologues abundance ratios are considerably different from the elemental ratio. The results of this work show that considering CO isotopologue ratios as constants can lead to an underestimate of disk masses by up to almost two orders of magnitude if grains have grown to larger sizes. This may explain observed discrepancies in mass determinations from different tracers. The dependence of the various isotopologues emission on stellar and disk parameters is investigated. Including CO isotope selective processes is crucial to determine the gas mass of the disk accurately (through ALMA observations) and thus to provide the amount of gas which may eventually form planets or change the dynamics of forming planetary systems.

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arXiv2014

Methanol Along the Path from Envelope to Protoplanetary Disc

Interstellar methanol is considered to be a parent species of larger, more complex organic molecules. A physicochemical simulation of infalling parcels of matter is performed for a low-mass star-forming system to trace the chemical evolution from cloud to disc. An axisymmetric 2D semi-analytic model generates the time-dependent density and velocity distributions, and full continuum radiative transfer is performed to calculate the dust temperature and the UV radiation field at each position as a function of time. A comprehensive gas-grain chemical network is employed to compute the chemical abundances along infall trajectories. Two physical scenarios are studied, one in which the dominant disc growth mechanism is viscous spreading, and another in which continuous infall of matter prevails. The results show that the infall path influences the abundance of methanol entering each type of disc, ranging from complete loss of methanol to an enhancement by a factor of > 1 relative to the prestellar phase. Critical chemical processes and parameters for the methanol chemistry under different physical conditions are identified. The exact abundance and distribution of methanol is important for the budget of complex organic molecules in discs, which will be incorporated into forming planetary system objects such as protoplanets and comets. These simulations show that the comet-forming zone contains less methanol than in the precollapse phase, which is dominantly of prestellar origin, but also with additional layers built up in the envelope during infall. Such intriguing links will soon be tested by upcoming data from the Rosetta mission.

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arXiv2014

Photodissociation and chemistry of N$_2$ in the circumstellar envelope of carbon-rich AGB stars

The envelopes of AGB stars are irradiated externally by ultraviolet photons; hence, the chemistry is sensitive to the photodissociation of N$_2$ and CO, which are major reservoirs of nitrogen and carbon, respectively. The photodissociation of N$_2$ has recently been quantified by laboratory and theoretical studies. Improvements have also been made for CO photodissociation. For the first time, we use accurate N$_2$ and CO photodissociation rates and shielding functions in a model of the circumstellar envelope of the carbon-rich AGB star, IRC +10216. We use a state-of-the-art chemical model of an AGB envelope, the latest CO and N$_2$ photodissociation data, and a new method for implementing molecular shielding functions in full spherical geometry with isotropic incident radiation. We compare computed column densities and radial distributions of molecules with observations. The transition of N$_2$ $\to$ N (also, CO $\to$ C $\to$ C$^+$) is shifted towards the outer envelope relative to previous models. This leads to different column densities and radial distributions of N-bearing species, especially those species whose formation/destruction processes largely depend on the availability of atomic or molecular nitrogen, for example, C$_n$N ($n$=1, 3, 5), C$_n$N$^-$ ($n$=1, 3, 5), HC$_n$N ($n$=1, 3, 5, 7, 9), H$_2$CN and CH$_2$CN. The chemistry of many species is directly or indirectly affected by the photodissociation of N$_2$ and CO, especially in the outer shell of AGB stars where photodissociation is important. Thus, it is important to include N$_2$ and CO shielding in astrochemical models of AGB envelopes and other irradiated environments. In general, while differences remain between our model of IRC +10216 and the observed molecular column densities, better agreement is found between the calculated and observed radii of peak abundance.

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arXiv2014

Water and methanol in low-mass protostellar outflows: gas-phase synthesis, ice sputtering and destruction

Water in outflows from protostars originates either as a result of gas-phase synthesis from atomic oxygen at T > 200 K, or from sputtered ice mantles containing water ice. We aim to quantify the contribution of the two mechanisms that lead to water in outflows, by comparing observations of gas-phase water to methanol (a grain surface product) towards three low-mass protostars in NGC1333. In doing so, we also quantify the amount of methanol destroyed in outflows. To do this, we make use of JCMT and Herschel-HIFI data of H2O, CH3OH and CO emission lines and compare them to RADEX non-LTE excitation simulations. We find up to one order of magnitude decrease in the column density ratio of CH3OH over H2O as the velocity increases in the line wings up to ~15 km/s. An independent decrease in X(CH3OH) with respect to CO of up to one order of magnitude is also found in these objects. We conclude that gas-phase formation of H2O must be active at high velocities (above 10 km/s, relative to the source velocity) to re-form the water destroyed during sputtering. In addition, the transition from sputtered water at low velocities to formed water at high velocities must be gradual. We place an upper limit of two orders of magnitude on the destruction of methanol by sputtering effects.

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arXiv2014

Effects of Reagent Rotation and Vibration on H + OH (v,j) $\to$ O + H2

The dynamics of the reaction H + OH $\to$ O (3P) + H2 have been studied in a series of quasi-classical trajectory (QCT) calculations and transition state theory (TST) methods using high quality 3A' and 3A'' potential energy surfaces (PESs). Accurate OH (v, j) state resolved cross sections and rate constants on both potential energy surfaces are presented and fitted for OH at (v = 0, j = 0-16) and (v = 1, j = 0-6). The cross sections were calculated for different collisional energies (Ec), ranging from the threshold energy at each specific rovibrational state up to 1.0 eV with step sizes of 0.1 eV or less. They increase steeply with collision energy when the barrier to reaction can be overcome, after which the cross sections stay nearly constant with energy. State resolved rate constants in the temperature range 200-2500 K are presented based on the cross sections. Total thermal rate constants were calculated by summing the rates for reaction on the 3A' and 3A'' potential energy surfaces weighted by 1/3 and taking into account the thermal populations of the rovibrational states of the OH molecules. It is shown that the improved canonical variational transition (CVT) treatments with the approximation of zero-curvature tunneling (ZCT) or small-curvature tunneling (SCT) produce results more in accord with the QCT results than the TST and CVT methods. The reactions are governed by the direct reaction mechanism. The rate constants for OH in excited vibrational and rotational states are orders of magnitude larger than the thermal rate constants, which needs to be taken into account in astrochemical models.

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arXiv2014

Water: from clouds to planets

Results from recent space missions, in particular Spitzer and Herschel, have lead to significant progress in our understanding of the formation and transport of water from clouds to disks, planetesimals, and planets. In this review, we provide the underpinnings for the basic molecular physics and chemistry of water and outline these advances in the context of water formation in space, its transport to a forming disk, its evolution in the disk, and finally the delivery to forming terrestrial worlds and accretion by gas giants. Throughout, we pay close attention to the disposition of water as vapor or solid and whether it might be subject to processing at any stage. The context of the water in the solar system and the isotopic ratios (D/H) in various bodies are discussed as grounding data point for this evolution. Additional advances include growing knowledge of the composition of atmospheres of extra-solar gas giants, which may be influenced by the variable phases of water in the protoplanetary disk. Further, the architecture of extra-solar systems leaves strong hints of dynamical interactions, which are important for the delivery of water and subsequent evolution of planetary systems. We conclude with an exploration of water on Earth and note that all of the processes and key parameters identified here should also hold for exoplanetary systems.

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arXiv2014

Warm formaldehyde in the Oph IRS 48 transitional disk

Simple molecules like H2CO and CH3OH in protoplanetary disks are the starting point for the production of more complex organic molecules. So far, the observed chemical complexity in disks has been limited due to freeze out of molecules onto grains in the bulk of the cold outer disk. Complex molecules can be studied more directly in transitional disks with large inner holes, as these have a higher potential of detection, through UV heating of the outer disk and the directly exposed midplane at the wall. We use Atacama Large Millimeter/submillimeter Array (ALMA) Band 9 (~680 GHz) line data of the transitional disk Oph IRS 48, previously shown to have a large dust trap, to search for complex molecules in regions where planetesimals are forming. We report the detection of the H2CO 9(1,8)-8(1,7) line at 674 GHz, which is spatially resolved as a semi-ring at ~60 AU radius centered south from the star. The inferred H2CO abundance is ~10^{-8} derived by combining a physical disk model of the source with a non-LTE excitation calculation. Upper limits for CH3OH lines in the same disk give an abundance ratio H2CO/CH3OH>0.3, which points to both ice formation and gas-phase routes playing a role in the H2CO production. Upper limits on the abundances of H13CO+, CN and several other molecules in the disk are also derived and found to be consistent with full chemical models. The detection of the H2CO line demonstrates the start of complex organic molecules in a planet-forming disk. Future ALMA observations should be able to push down the abundance detection limits of other molecules by 1-2 orders of magnitude and test chemical models of organic molecules in (transitional) disks.

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