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C. Joblin

Publications and source records attributed to C. Joblin.

At least 37 records · Page 2Linked to original sources

Mixed aliphatic and aromatic composition of evaporating very small grains in NGC 7023 revealed by the 3.4/3.3 $μ$m ratio

In photon-dominated regions (PDRs), UV photons from nearby stars lead to the evaporation of very small grains (VSGs) and the production of gas-phase polycyclic aromatic hydrocarbons (PAHs). Our goal is to achieve better insight into the composition and evolution of evaporating very small grains (eVSGs) and PAHs through analyzing the infrared (IR) aliphatic and aromatic emission bands. We combined spectro-imagery in the near- and mid-IR to study the spatial evolution of the emission bands in the prototypical PDR NGC 7023. We used near-IR spectra obtained with AKARI to trace the evolution of the 3.3$μ$m and 3.4$μ$m bands, which are associated with aromatic and aliphatic C-H bonds on PAHs. The spectral fitting involves an additional broad feature centred at 3.45$μ$m. Mid-IR observations obtained with Spitzer are used to discriminate the signatures of eVSGs, neutral and cationic PAHs. We correlated the spatial evolution of all these bands with the intensity of the UV field to explore the processing of their carriers. The intensity of the 3.45$μ$m plateau shows an excellent correlation with that of the 3.3$μ$m aromatic band (correlation coefficient R = 0.95), indicating that the plateau is dominated by the emission from aromatic bonds. The ratio of the 3.4$μ$m and 3.3$μ$m band intensity ($I_{3.4}/I_{3.3}$) decreases by a factor of 4 at the PDR interface from the more UV-shielded to the more exposed layers. The transition region between the aliphatic and aromatic material is found to correspond spatially with the transition zone between neutral PAHs and eVSGs. We conclude that the photo-processing of eVSGs leads to the production of PAHs with attached aliphatic sidegroups that are revealed by the 3.4$μ$m emission band. Our analysis provides evidence for the presence of very small grains of mixed aromatic and aliphatic composition in PDRs.

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The chemistry and spatial distribution of small hydrocarbons in UV-irradiated molecular clouds: the Orion Bar PDR

We study the spatial distribution and chemistry of small hydrocarbons in the Orion Bar PDR. We used the IRAM-30m telescope to carry out a millimetre line survey towards the Orion Bar edge, complemented with ~2'x2' maps of the C2H and c-C3H2 emission. We analyse the excitation of the detected hydrocarbons and constrain the physical conditions of the emitting regions with non-LTE radiative transfer models. We compare the inferred column densities with updated gas-phase photochemical models including 13CCH and C13CH isotopomer fractionation. ~40% of the lines in the survey arise from hydrocarbons (C2H, C4H, c-C3H2, c-C3H, C13CH, 13CCH, l-C3H and l-H2C3). We detect new lines from l-C3H+ and improve its rotational spectroscopic constants. Anions or deuterated hydrocarbons are not detected: [C2D]/[C2H]<0.2%, [C2H-]/[C2H]<0.007% and [C4H-]/[C4H]<0.05%. Our gas-phase models can reasonably match the observed column densities of most hydrocarbons (within factors <3). Since the observed spatial distribution of the C2H and c-C3H2 emission is similar but does not follow the PAH emission, we conclude that, in high UV-flux PDRs, photodestruction of PAHs is not a necessary requirement to explain the observed abundances of the smallest hydrocarbons. Instead, gas-phase endothermic reactions (or with barriers) between C+, radicals and H2 enhance the formation of simple hydrocarbons. Observations and models suggest that the [C2H]/[c-C3H2] ratio (~32 at the PDR edge) decreases with the UV field attenuation. The observed low cyclic-to-linear C3H column density ratio (<3) is consistent with a high electron abundance (Xe) PDR environment. In fact, the poorly constrained Xe gradient influences much of the hydrocarbon chemistry in the more UV-shielded gas. We propose that reactions of C2H isotopologues with 13C+ and H atoms can explain the observed [C13CH]/[13CCH]=1.4(0.1) fractionation level.

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Physical structure of the photodissociation regions in NGC 7023. Observations of gas and dust emission with Herschel

The determination of the physical conditions in molecular clouds is a key step towards our understanding of their formation and evolution of associated star formation. We investigate the density, temperature, and column density of both dust and gas in the photodissociation regions (PDRs) located at the interface between the atomic and cold molecular gas of the NGC 7023 reflection nebula. We study how young stars affect the gas and dust in their environment. Our approach combining both dust and gas delivers strong constraints on the physical conditions of the PDRs. We find dense and warm molecular gas of high column density in the PDRs.

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Kinematics of the ionized-to-neutral interfaces in Monoceros R2

Context. Monoceros R2 (Mon R2), at a distance of 830 pc, is the only ultra-compact H ii region (UC H ii) where its associated photon-dominated region (PDR) can be resolved with the Herschel Space Observatory. Aims. Our aim is to investigate observationally the kinematical patterns in the interface regions (i.e., the transition from atomic to molecular gas) associated with Mon R2. Methods. We used the HIFI instrument onboard Herschel to observe the line profiles of the reactive ions CH+, OH+ and H2O+ toward different positions in Mon R2. We derive the column density of these molecules and compare them with gas-phase chemistry models. Results. The reactive ion CH+ is detected both in emission (at central and red-shifted velocities) and in absorption (at blue-shifted velocities). OH+ is detected in absorption at both blue- and red-shifted velocities, with similar column densities. H2O+ is not detected at any of the positions, down to a rms of 40 mK toward the molecular peak. At this position, we find that the OH+ absorption originates in a mainly atomic medium, and therefore is associated with the most exposed layers of the PDR. These results are consistent with the predictions from photo-chemical models. The line profiles are consistent with the atomic gas being entrained in the ionized gas flow along the walls of the cavity of the H ii region. Based on this evidence, we are able to propose a new geometrical model for this region. Conclusions. The kinematical patterns of the OH+ and CH+ absorption indicate the existence of a layer of mainly atomic gas for which we have derived, for the first time, some physical parameters and its dynamics.

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Unveiling the dust nucleation zone of IRC+10216 with ALMA

We report the detection in IRC+10216 of lines of HNC $J$=3-2 pertaining to 9 excited vibrational states with energies up to $\sim$5300 K. The spectrum, observed with ALMA, also shows a surprising large number of narrow, unidentified lines that arise in the vicinity of the star. The HNC data are interpreted through a 1D--spherical non--local radiative transfer model, coupled to a chemical model that includes chemistry at thermochemical equilibrium for the innermost regions and reaction kinetics for the external envelope. Although unresolved by the present early ALMA data, the radius inferred for the emitting region is $\sim$0.06'' (i.e., $\simeq$ 3 stellar radii), similar to the size of the dusty clumps reported by IR studies of the innermost region ($r <$ 0.3''). The derived abundance of HNC relative to H$_2$ is $10^{-8} <$ $χ$(HNC) $< 10^{-6}$, and drops quickly where the gas density decreases and the gas chemistry is dominated by reaction kinetics. Merging HNC data with that of molecular species present throughout the inner envelope, such as vibrationally excited HCN, SiS, CS, or SiO, should allow us to characterize the physical and chemical conditions in the dust formation zone.

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The Far-IR View of Star and Planet Forming Regions

The far-IR range is a critical wavelength range to characterize the physical and chemical processes that transform the interstellar material into stars and planets. Objects in the earliest phases of stellar and planet evolution release most of their energy at these long wavelengths. In this contribution we briefly summarise some of the most relevant scientific advances achieved by the Herschel Space Observatory in the field. We also anticipate those that will be made possible by the large increase in sensitivity of SPICA cooled telescope. It is concluded that only through sensitive far-IR observations much beyond Herschel capabilities we will be able to constrain the mass, the energy budget and the water content of hundreds of protostars and planet-forming disks.

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Spatial distribution of small hydrocarbons in the neighborhood of the Ultra Compact HII region Monoceros R2

We study the chemistry of small hydrocarbons in the photon-dominated regions (PDRs) associated with the ultra-compact HII region Mon R2. Our goal is to determine the variations of the abundance of small hydrocarbons in a high-UV irradiated PDR and investigate their chemistry. We present an observational study of CH, CCH and c-C$_3$H$_2$ in Mon R2 combining data obtained with the IRAM 30m telescope and Herschel. We determine the column densities of these species, and compare their spatial distributions with that of polycyclic aromatic hydrocarbon (PAH). We compare the observational results with different chemical models to explore the relative importance of gas-phase, grain-surface and time-dependent chemistry in these environments. The emission of the small hydrocarbons show different patterns. The CCH emission is extended while CH and c-C$_3$H$_2$ are concentrated towards the more illuminated layers of the PDR. The ratio of the column densities of c-C$_3$H$_2$ and CCH shows spatial variations up to a factor of a few, increasing from $N(c-C$_3$H$_2$)/N(CCH)\approx0.004$ in the envelope to a maximum of $\sim0.015-0.029$ towards the 8$μ$m emission peak. Comparing these results with other galactic PDRs, we find that the abundance of CCH is quite constant over a wide range of G$_0$, whereas the abundance of c-C$_3$H$_2$ is higher in low-UV PDRs. In Mon R2, the gas-phase steady-state chemistry can account relatively well for the abundances of CH and CCH in the most exposed layers of the PDR, but falls short by a factor of 10 to reproduce c-C$_3$H$_2$. In the molecular envelope, time-dependent effects and grain surface chemistry play a dominant role in determining the hydrocarbons abundances. Our study shows that CCH and c-C$_3$H$_2$ present a complex chemistry in which UV photons, grain-surface chemistry and time dependent effects contribute to determine their abundances.

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Evolution of PAHs in photodissociation regions: Hydrogenation and charge states

Various studies have emphasized variations of the charge state and composition of the interstellar polycyclic aromatic hydrocarbon (PAH) population in photodissociation regions (PDRs). We aim to model the spatial evolution of the charge and hydrogenation states of PAHs in PDRs. We focus on the specific case of the north-west (NW) PDR of NGC 7023 and also discuss the case of the diffuse interstellar medium (ISM). The physical conditions in NGC 7023 NW are modelled using a state-of-the-art PDR code. We then use a new PAH chemical evolution model that includes recent experimental data on PAHs and describes multiphoton events. We consider a family of compact PAHs bearing up to 96 carbon atoms. The calculated ionization ratio is in good agreement with observations in NGC 7023 NW. Within the PDR, PAHs evolve into three major populations: medium-sized PAHs (50 90) can be superhydrogenated, and smaller species (Nc<50) are fully dehydrogenated. In the cavity, where the fullerene C60 was recently detected, all the studied PAHs are found to be quickly fully dehydrogenated. PAH chemical evolution exhibits a complex non-linear behaviour as a function of the UV radiation field because of multiphoton events. Steady state for hydrogenation is reached on timescales ranging from less than a year for small PAHs, up to 10000 years for large PAHs at Av=1. We identified critical reactions that need more studies. Our new model allows us to rationalize the observational constraints without any fitting parameter. PAHs smaller than 50 carbon atoms are not expected to survive in the NGC 7023 NW PDR. A similar conclusion is obtained for the diffuse ISM. Carbon clusters turn out to be end products of PAH photodissociation, and the evolution of these clusters needs to be investigated further to evaluate their impact on the chemical and physical evolution of PDRs.

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The chemistry of ions in the Orion Bar I. - CH+, SH+, and CF+: The effect of high electron density and vibrationally excited H2 in a warm PDR surface

The abundances of interstellar CH+ and SH+ are not well understood as their most likely formation channels are highly endothermic. Using data from Herschel, we study the formation of CH+ and SH+ in a typical high UV-illumination photon-dominated region (PDR), the Orion Bar. Herschel/HIFI provides velocity-resolved data of CH+ 1-0 and 2-1 and three hyperfine transitions of SH+. Herschel/PACS provides information on the excitation and spatial distribution of CH+ (up to J=6-5). The widths of the CH+ 2-1 and 1-0 transitions are of ~5 km/s, significantly broader than the typical width of dense gas tracers in the Orion Bar (2-3 km/s) and are comparable to the width of tracers of the interclump medium such as C+ and HF. The detected SH+ transitions are narrower compared to CH+ and have line widths of 3 km/s, indicating that SH+ emission mainly originates in denser condensations. Non-LTE radiative transfer models show that electron collisions affect the excitation of CH+ and SH+, and that reactive collisions need to be taken into account to calculate the excitation of CH+. Comparison to PDR models shows that CH+ and SH+ are tracers of the warm surface region (AV<1.5) of the PDR with temperatures between 500-1000 K. We have also detected the 5-4 transition of CF+ (FWHM=1.9 km/s) with an intensity that is consistent with previous observations of lower-J CF+ transitions toward the Orion Bar. A comparison to PDR models indicate that the internal vibrational energy of H2 can explain the formation of CH+ for typical physical conditions in the Orion Bar near the ionization front. H2 vibrational excitation is the most likely explanation of SH+ formation as well. The abundance ratios of CH+ and SH+ trace the destruction paths of these ions, and through that, indirectly, the ratios of H, H2 and electron abundances as a function of depth into the cloud.

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The chemistry of C3 & Carbon Chain Molecules in DR21(OH)

(Abridged) We have observed velocity resolved spectra of four ro-vibrational far-infrared transitions of C3 between the vibrational ground state and the low-energy nu2 bending mode at frequencies between 1654--1897 GHz using HIFI on board Herschel, in DR21(OH), a high mass star forming region. Several transitions of CCH and c-C3H2 have also been observed with HIFI and the IRAM 30m telescope. A gas and grain warm-up model was used to identify the primary C3 forming reactions in DR21(OH). We have detected C3 in absorption in four far-infrared transitions, P(4), P(10), Q(2) and Q(4). The continuum sources MM1 and MM2 in DR21(OH) though spatially unresolved, are sufficiently separated in velocity to be identified in the C3 spectra. All C3 transitions are detected from the embedded source MM2 and the surrounding envelope, whereas only Q(4) & P(4) are detected toward the hot core MM1. The abundance of C3 in the envelope and MM2 is \sim6x10^{-10} and \sim3x10^{-9} respectively. For CCH and c-C3H2 we only detect emission from the envelope and MM1. The observed CCH, C3, and c-C3H2 abundances are most consistent with a chemical model with n(H2)\sim5x10^{6} cm^-3 post-warm-up dust temperature, T_max =30 K and a time of \sim0.7-3 Myr. Post warm-up gas phase chemistry of CH4 released from the grain at t\sim 0.2 Myr and lasting for 1 Myr can explain the observed C3 abundance in the envelope of DR21(OH) and no mechanism involving photodestruction of PAH molecules is required. The chemistry in the envelope is similar to the warm carbon chain chemistry (WCCC) found in lukewarm corinos. The observed lower C3 abundance in MM1 as compared to MM2 and the envelope could be indicative of destruction of C3 in the more evolved MM1. The timescale for the chemistry derived for the envelope is consistent with the dynamical timescale of 2 Myr derived for DR21(OH) in other studies.

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Herschel / HIFI observations of CO, H2O and NH3 in Mon R2

Context. Mon R2 is the only ultracompact HII region (UCHII) where the associated photon-dominated region (PDR) can be resolved with Herschel. Due to its brightness and proximity, it is the best source to investigate the chemistry and physics of highly UV-irradiated PDRs. Aims. Our goal is to estimate the abundance of H2O and NH3 in this region and investigate their origin. Methods. We present new observations obtained with HIFI and the IRAM-30m telescope. Using a large velocity gradient approach, we model the line intensities and derive an average abundance of H2O and NH3 across the region. Finally, we model the line profiles with a non-local radiative transfer model and compare these results with the abundance predicted by the Meudon PDR code. Results. The variations of the line profiles and intensities indicate complex geometrical and kinematical patterns. The H2O lines present a strong absorption at the ambient velocity and emission in high velocity wings towards the HII region. The spatial distribution of the o-H2^18O line shows that the its emission arises in the PDR surrounding the HII region. By modeling the o-H2^18O emission we derive a mean abundance of o-H2O of ~10^-8 relative to H2. The ortho-H2O abundance is however larger, ~1x10^-7, in the high velocity wings. Possible explanations for this larger abundance include an expanding hot PDR and/or an outflow. Ammonia seems to be present only in the envelope with an average abundance of ~2x10^-9 relative to H2. Conclusions. The Meudon PDR code can account for the measured water abundance in the high velocity gas as long as we assume that it originates from a <1 mag hot expanding layer of the PDR, i.e. that the outflow has only a minor contribution to this emission. To explain the abundances in the rest of the cloud the molecular freeze out and grain surface chemistry would need to be included.

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Evaporating Very Small Grains as tracers of the UV radiation field in Photo-dissociation Regions

Context. In photo-dissociation regions (PDRs), Polycyclic Aromatic Hydrocarbons (PAHs) could be produced by evaporation of Very Small Grains (VSGs) by the impinging UV radiation field from a nearby star. Aims. We investigate quantitatively the transition zone between evaporating Very Small Grains (eVSGs) and PAHs in several PDRs. Methods. We study the relative contribution of PAHs and eVSGs to the mid-IR emission in a wide range of excitation conditions. We fit the observed mid-IR emission of PDRs by using a set of template band emission spectra of PAHs, eVSGs and gas lines. The fitting tool PAHTAT (PAH Toulouse Astronomical Templates) is made available to the community as an IDL routine. From the results of the fit, we derive the fraction of carbon f_eVSG locked in eVSGs and compare it to the intensity of the local UV radiation field. Results. We show a clear decrease of f_eVSG with increasing intensity of the local UV radiation field, which supports the scenario of photo-destruction of eVSGs. Conversely, this dependence can be used to quantify the intensity of the UV radiation field for different PDRs, including non resolved ones. Conclusions. PAHTAT can be used to trace the intensity of the local UV radiation field in regions where eVSGs evaporate, which correspond to relatively dense (nH = [100, 10^5 ] cm-3) and UV irradiated PDRs (G0 = [100, 5x10^4]) where H2 emits in rotational lines.

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Spectral line survey of the ultracompact HII region Mon R2

Ultracompact (UC) HII regions constitute one of the earliest phases in the formation of a massive star and are characterized by extreme physical conditions (Go>10^5 Habing field and n>10^6 cm^-3). The UC HII Mon R2 is the closest one and therefore an excellent target to study the chemistry in these complex regions. We carried out a 3mm and 1mm spectral survey using the IRAM 30-m telescope towards three positions that represent different physical environments in Mon R2: (i) the ionization front (IF) at (0",0"); two peaks in the molecular cloud (ii) MP1 at the offset (+15",-15") and (iii) MP2 at the farther offset (0",40"). In addition, we carried out extensive modeling to explain the chemical differences between the three observed regions. We detected more than thirty different species. We detected SO+ and C4H suggesting that UV radiation plays an important role in the molecular chemistry of this region. We detected the typical PDR molecules CN, HCN, HCO, C2H, and c-C3H2. While the IF and the MP1 have a chemistry similar to that found in high UV field and dense PDRs like the Orion Bar, the MP2 is more similar to lower UV/density PDRs like the Horsehead nebula. We also detected complex molecules that are not usually found in PDRs (CH3CN, H2CO, HC3N, CH3OH and CH3C2H). Sulfur compounds CS, HCS+, C2S, H2CS, SO and SO2 and the deuterated species DCN and C2D were also identified. [DCN]/[HCN]=0.03 and [C2D]/[C2H]=0.05, are among the highest in warm regions. Our results show that the high UV/dense PDRs present a different chemistry from that of the low UV case. Abundance ratios like [CO+]/[HCO+] or [HCO]/[HCO+] are good diagnostics to differentiate between them. In Mon R2 we have the two classes of PDRs, a high UV PDR towards the IF and the adjacent molecular bar and a low-UV PDR which extends towards the north-west following the border of the cloud.

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Spatial variation of the cooling lines in the Orion Bar from Herschel/PACS

We present spatially resolved Herschel/PACS observations of the Orion Bar. We have characterise the emission of the far-infrared fine-structure lines of [CII] (158um), [OI] (63 and 145um), and [NII] (122um) that trace the gas local conditions. The observed distribution and variation of the lines are discussed in relation to the underlying geometry and linked to the energetics associated with the Trapezium stars. These observations enable us to map the spatial distribution of these fine-structure lines with a spatial resolution between 4" and 11" and covering a total square area of about 120"x105". The spatial profile of the emission lines are modelled using the radiative transfer code Cloudy. We find that the spatial distribution of the [CII] line coincides with that of the [OI] lines. The [NII] line peaks closer to the ionising star than the other three lines, but with a small region of overlap. We can distinguish several knots of enhanced emission within the Bar indicating the presence of an inhomogenous and structured medium. The emission profiles cannot be reproduced by a single photo-dissociation region, clearly indicating that, besides the Bar, there is a significant contribution from additional photo-dissociation region(s) over the area studied. The combination of both the [NII] and [OI] 145um lines can be used to estimate the [CII] emission and distinguish between its ionised or neutral origin. We have calculated how much [CII] emission comes from the neutral and ionised region, and find that at least 82% originates from the photo-dissocciation region. Together, the [CII] 158um and [OI] 63 and 145um lines account for 90% of the power emitted by the main cooling lines in the Bar (including CO, H2, etc...), with [OI] 63um alone accounting for 72% of the total.

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Fusion between ground- and space-based mid-infrared observations

Mid-infrared astronomy (operating at wavelengths ranging from 2 to 25 $μ$m) has progressed significantly in the last decades, thanks to the improvement of detector techniques and the growing diameter of telescopes. Space observatories benefit from the absence of atmospheric absorption, allowing to reach the very high sensitivities needed to perform 3D hyperspectral observations, but telescopes are limited in diameter ($< 1$ meter) and therefore provide observations at low angular resolution (typically a few seconds of arc). On the other hand, ground-based facilities suffer from strong atmospheric absorption but use large telescopes (above 8m diameter) to perform sub-arcsecond angular resolution imaging through selected windows in the mid-infrared range. In this Paper, we present a method based on Lee and Seung's Non-negative Matrix Factorization (NMF) to merge data from space and ground based mid-infrared (mid-IR) telescopes in order to combine the best sensitivity, spectral coverage and angular resolution. We prove the efficiency of this technique when applied to real mid-IR astronomical data. We suggest that this method can be applied to any combination of low and high spatial resolution positive hyperspectral datasets, as long as the spectral variety of the data allows decomposition into components using NMF.

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OH emission from warm and dense gas in the Orion Bar PDR

As part of a far-infrared (FIR) spectral scan with Herschel/PACS, we present the first detection of the hydroxyl radical (OH) towards the Orion Bar photodissociation region (PDR). Five OH rotational Lambda-doublets involving energy levels out to E_u/k~511 K have been detected (at ~65, ~79, ~84, ~119 and ~163um). The total intensity of the OH lines is I(OH)~5x10^-4 erg s^-1 cm^-2 sr^-1. The observed emission of rotationally excited OH lines is extended and correlates well with the high-J CO and CH^+ J=3-2 line emission (but apparently not with water vapour), pointing towards a common origin. Nonlocal, non-LTE radiative transfer models including excitation by the ambient FIR radiation field suggest that OH arises in a small filling factor component of warm (Tk~160-220 K) and dense (n_H~10^{6-7} cm^-3) gas with source-averaged OH column densities of ~10^15 cm^-2. High density and temperature photochemical models predict such enhanced OH columns at low depths (A_V<1) and small spatial scales (~10^15 cm), where OH formation is driven by gas-phase endothermic reactions of atomic oxygen with molecular hydrogen. We interpret the extended OH emission as coming from unresolved structures exposed to far-ultraviolet (FUV) radiation near the Bar edge (photoevaporating clumps or filaments) and not from the lower density "interclump" medium. Photodissociation leads to OH/H2O abundance ratios (>1) much higher than those expected in equally warm regions without enhanced FUV radiation fields.

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Herschel observations of Extra-Ordinary Sources: Methanol as a probe of physical conditions in Orion KL

We have examined methanol emission from Orion KL with of the {\em Herschel}/HIFI instrument, and detected two methanol bands centered at 524 GHz and 1061 GHz. The 524 GHz methanol band (observed in HIFI band 1a) is dominated by the isolated $Δ$J$=$0, K$=-4\rightarrow$-3, v$_t$$=$0 Q branch, and includes 25 E-type and 2 A-type transitions. The 1061 GHz methanol band (observed in HIFI band 4b) is dominated by the $Δ$J$=$0, K$=7\rightarrow$6, v$_t$$=$0 Q branch transitions which are mostly blended. We have used the isolated E-type v$_t$$=$0 methanol transitions to explore the physical conditions in the molecular gas. With HIFI's high velocity resolution, the methanol emission contributed by different spatial components along the line of sight toward Orion KL (hot core, low velocity flow, and compact ridge) can be distinguished and studied separately. The isolated transitions detected in these bands cover a broad energy range (upper state energy ranging from 80 K to 900 K), which provides a unique probe of the thermal structure in each spatial component. The observations further show that the compact ridge is externally heated. These observations demonstrate the power of methanol lines as probes of the physical conditions in warm regions in close proximity to young stars.

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Detection of OH$^+$ and H$_2$O$^+$ towards Orion~KL

We report observations of the reactive molecular ions OH$^+$, H$_2$O$^+$, and H$_3$O$^+$ towards Orion KL with Herschel/HIFI. All three $N=1-0$ fine-structure transitions of OH$^+$ at 909, 971, and 1033GHz and both fine-structure components of the doublet {\it ortho}-H$_2$O$^+$ $1_{11}-0_{00}$ transition at 1115 and 1139GHz were detected; an upper limit was obtained for H$_3$O$^+$. OH$^+$ and H$_2$O$^+$ are observed purely in absorption, showing a narrow component at the source velocity of 9 kms$^{-1}$, and a broad blueshifted absorption similar to that reported recently for HF and {\it para}-H$_{2}^{18}$O, and attributed to the low velocity outflow of Orion KL. We estimate column densities of OH$^+$ and H$_2$O$^+$ for the 9 km s$^{-1}$ component of $9 \pm 3 \times 10^{12}$cm$^{-2}$ and $7 \pm 2 \times 10^{12}$cm$^{-2}$, and those in the outflow of $1.9 \pm 0.7 \times 10^{13}$cm$^{-2}$ and $1.0 \pm 0.3 \times 10^{13}$cm$^{-2}$. Upper limits of $2.4\times 10^{12}$cm$^{-2}$ and $8.7\times 10^{12}$cm$^{-2}$ were derived for the column densities of {\it ortho} and {\it para}-H$_3$O$^+$ from transitions near 985 and 1657GHz. The column densities of the three ions are up to an order of magnitude lower than those obtained from recent observations of W31C and W49N. The comparatively low column densities may be explained by a higher gas density despite the assumption of a very high ionization rate.

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