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.Comment: 13 pages, 11 figures. Accepted for publication in A&A. Typos correcte

Mixed aliphatic and aromatic composition of evaporating very small grains in NGC 7023 revealed by the 3.4/3.3 μ\mum 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$\mu$m and 3.4$\mu$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$\mu$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$\mu$m plateau shows an excellent correlation with that of the 3.3$\mu$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$\mu$m and 3.3$\mu$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$\mu$m emission band. Our analysis provides evidence for the presence of very small grains of mixed aromatic and aliphatic composition in PDRs.Comment: Accepted for publication in A&A. Abstract abridged, language editing applied in v

Polycyclic aromatic hydrocarbons and molecular hydrogen in oxygen-rich planetary nebulae: the case of NGC6720

Evolved stars are primary sources for the formation of polycyclic aromatic hydrocarbons (PAHs) and dust grains. Their circumstellar chemistry is usually designated as either oxygen-rich or carbon-rich, although dual-dust chemistry objects, whose infrared spectra reveal both silicate- and carbon-dust features, are also known. The exact origin and nature of this dual-dust chemistry is not yet understood. Spitzer-IRS mid-infrared spectroscopic imaging of the nearby, oxygen-rich planetary nebula NGC6720 reveals the presence of the 11.3 micron aromatic (PAH) emission band. It is attributed to emission from neutral PAHs, since no band is observed in the 7 to 8 micron range. The spatial distribution of PAHs is found to closely follow that of the warm clumpy molecular hydrogen emission. Emission from both neutral PAHs and warm H2 is likely to arise from photo-dissociation regions associated with dense knots that are located within the main ring. The presence of PAHs together with the previously derived high abundance of free carbon (relative to CO) suggest that the local conditions in an oxygen-rich environment can also become conducive to in-situ formation of large carbonaceous molecules, such as PAHs, via a bottom-up chemical pathway. In this scenario, the same stellar source can enrich the interstellar medium with both oxygen-rich dust and large carbonaceous molecules.Comment: Accepted by MNRAS. 5 page

Detection of the buckminsterfullerene cation (C60+) in space

In the early 90s, C60+ was proposed as the carrier of two diffuse interstellar bands (DIBs) at 957.7 and 963.2 nm, but a firm identification still awaits gas-phase spectroscopic data. Neutral C60, on the other hand, was recently detected through its infrared emission bands in the interstellar medium and evolved stars. In this contribution, we present the detection of C60+ through its infrared vibrational bands in the NGC 7023 nebula, based on spectroscopic observations with the Spitzer space telescope, quantum chemistry calculation, and laboratory data from the literature. This detection supports the idea that C60+ could be a DIB carrier, and provides robust evidence that fullerenes exist in the gas-phase in the interstellar medium. Modeling efforts to design specific observations, combined with new gas-phase data, will be essential to confirm this proposal. A definitive attribution of the 957.7 and 963.2 nm DIBs to C60+ would represent a significant step forward in the field.Comment: To appear in "Proceedings of IAU 297 symposium on the Diffuse Interstellar Bands", eds. J. Cami and N. Cox (5 pages

Variations in solar wind fractionation as seen by ACE/SWICS over a solar cycle and the implications for Genesis Mission results

We use ACE/SWICS elemental composition data to compare the variations in solar wind fractionation as measured by SWICS during the last solar maximum (1999-2001), the solar minimum (2006-2009) and the period in which the Genesis spacecraft was collecting solar wind (late 2001 - early 2004). We differentiate our analysis in terms of solar wind regimes (i.e. originating from interstream or coronal hole flows, or coronal mass ejecta). Abundances are normalized to the low-FIP ion magnesium to uncover correlations that are not apparent when normalizing to high-FIP ions. We find that relative to magnesium, the other low-FIP elements are measurably fractionated, but the degree of fractionation does not vary significantly over the solar cycle. For the high-FIP ions, variation in fractionation over the solar cycle is significant: greatest for Ne/Mg and C/Mg, less so for O/Mg, and the least for He/Mg. When abundance ratios are examined as a function of solar wind speed, we find a strong correlation, with the remarkable observation that the degree of fractionation follows a mass-dependent trend. We discuss the implications for correcting the Genesis sample return results to photospheric abundances.Comment: Accepted for publication in Ap

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.Comment: 6 pages, 5 figures. Accepted for publication in A&

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.Comment: 30 pages, 23 figures, 15 tables. Accepted for publication in A&A (English edited, abstract abridged

Mid-infrared PAH and H2 emission as a probe of physical conditions in extreme PDRs

Mid-infrared (IR) observations of polycyclic aromatic hydrocarbons (PAHs) and molecular hydrogen emission are a potentially powerful tool to derive physical properties of dense environments irradiated by intense UV fields. We present new, spatially resolved, \emph{Spitzer} mid-IR spectroscopy of the high UV-field and dense photodissocation region (PDR) around Monoceros R2, the closest ultracompact \hII region, revealing the spatial structure of ionized gas, PAHs and H$_2$ emissions. Using a PDR model and PAH emission feature fitting algorithm, we build a comprehensive picture of the physical conditions prevailing in the region. We show that the combination of the measurement of PAH ionization fraction and of the ratio between the H$_2$ 0-0 S(3) and S(2) line intensities, respectively at 9.7 and 12.3 $\mu$m, allows to derive the fundamental parameters driving the PDR: temperature, density and UV radiation field when they fall in the ranges $T = 250-1500$K, $n_H=10^4-10^6$cm$^{-3}$, $G_0=10^3-10^5$ respectively. These mid-IR spectral tracers thus provide a tool to probe the similar but unresolved UV-illuminated surface of protoplanetary disks or the nuclei of starburst galaxies.Comment: Accepted for publication in ApJ Letter

Interstellar C60+

Buckminsterfullerene (C60) was recently detected through its infrared emission bands in the interstellar medium (ISM), including in the proximity of massive stars, where physical conditions could favor the formation of the cationic form, C60+. In addition, C60+ was proposed as the carrier of two diffuse interstellar bands in the near-IR, although a firm identification still awaits for gas-phase spectroscopic data. We examined in details the Spitzer IRS spectra of the NGC 7023 reflection nebula, at a position close (7.5") to the illuminating B star HD 200775, and found four previously unreported bands at 6.4, 7.1, 8.2 and 10.5 \mu m in addition to the classical bands attributed to Polycylic Aromatic Hydrocarbons (PAHs) and neutral C60. These 4 bands are observed only in this region of the nebula, while C60 emission is still present slightly further away from the star, and PAH emission even further away. Based on this observation, on theoretical calculations we perform, and on laboratory studies, we attribute these bands to C60+. The detection of C60+ confirms the idea that large carbon molecules exist in the gas-phase in these environments. In addition, the relative variation of the C60, and C60+, band intensities constitutes a potentially powerful probe of the physical conditions in highly UV-irradiated regions.Comment: Accepted for publication in A&A, v2: minor corrections of typos and language and additional reference include

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$\mu$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.Comment: 18 pages, 11 figures, 7 tables. Proposed for acceptance in A&A. Abstract abridge