The Detection of a Hot Molecular Core in the Extreme Outer Galaxy

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Published 2021 December 1 © 2021. The American Astronomical Society. All rights reserved.
, , Citation Takashi Shimonishi et al 2021 ApJ 922 206 DOI 10.3847/1538-4357/ac289b

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0004-637X/922/2/206

Abstract

Interstellar chemistry in low-metallicity environments is crucial to understand chemical processes in the past metal-poor universe. Recent studies of interstellar molecules in nearby low-metallicity galaxies have suggested that metallicity has a significant effect on the chemistry of star-forming cores. Here we report the first detection of a hot molecular core in the extreme outer Galaxy, which is an excellent laboratory to study star formation and the interstellar medium in a Galactic low-metallicity environment. The target star-forming region, WB 89–789, is located at a galactocentric distance of 19 kpc. Our Atacama Large Millimeter/submillimeter Array observations in 241–246, 256–261, 337–341, and 349–353 GHz have detected a variety of carbon-, oxygen-, nitrogen-, sulfur-, and silicon-bearing species, including complex organic molecules (COMs) containing up to nine atoms, toward a warm (>100 K) and compact (<0.03 pc) region associated with a protostar (∼8 × 103 L). Deuterated species such as HDO, HDCO, D2CO, and CH2DOH are also detected. A comparison of fractional abundances of COMs relative to CH3OH between the outer Galactic hot core and an inner Galactic counterpart shows a remarkable similarity. On the other hand, the molecular abundances in the present source do not resemble those of low-metallicity hot cores in the Large Magellanic Cloud. The results suggest that great molecular complexity exists even in the primordial environment of the extreme outer Galaxy. The detection of another embedded protostar associated with high-velocity SiO outflows is also reported.

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1. Introduction

Understanding the star formation and interstellar medium (ISM) at low metallicity is crucial to unveil physical and chemical processes in the past Galactic environment or those in high-redshift galaxies, where the metallicity was significantly lower compared to the present-day solar neighborhood.

Hot molecular cores are one of the early stages of star formation, and they play a key role in the formation of the chemical complexity of the ISM. Physically, hot cores are defined as having a small source size (≲0.1 pc), high density (≳106 cm−3), and warm gas/dust temperature (≳100 K) (e.g., van Dishoeck & Blake 1998; Kurtz et al. 2000). The chemistry of hot cores is characterized by the sublimation of ice mantles, which accumulated over the course of star formation. In cold molecular clouds and prestellar cores, gaseous molecules and atoms are frozen onto dust grains. With dust temperatures increasing owing to star formation activities, chemical reactions among heavy species become active on grain surfaces, forming larger complex molecules (e.g., Garrod & Herbst 2006). In addition, sublimated molecules, such as CH3OH and NH3, are subject to further gas-phase reactions (e.g., Nomura & Millar 2004; Taquet et al. 2016). As a result, warm and dense gas around protostars become chemically rich, and embedded protostars are observed as one of the most powerful molecular line emitters, called a hot core. They are important targets for astrochemical studies of star-forming regions, because a variety of molecular species, including complex organic molecules (COMs), are often detected in hot cores (Herbst & van Dishoeck 2009 and references therein). Thus, detailed studies of the chemical properties of hot cores are important for understanding complex chemical processes triggered by star formation.

Recent ALMA (Atacama Large Millimeter/submillimeter Array) observations of hot molecular cores in a nearby low-metallicity galaxy, the Large Magellanic Cloud (LMC), have suggested that the metallicity has a significant effect on their molecular compositions (Shimonishi et al. 2016b, 2020; Sewiło et al. 2018); e.g., the metallicity of the LMC is ∼1/2–1/3 of the solar neighborhood. A comparison of molecular abundances between LMC and Galactic hot cores suggests that organic molecules (e.g., CH3OH, a classical hot-core tracer) show a large abundance variation in low-metallicity hot cores (Shimonishi et al. 2020). There are organic-poor hot cores that are unique to the LMC (Shimonishi et al. 2016b), while there are relatively organic-rich hot cores, where the abundances of organic molecules roughly scale with the metallicity (Sewiło et al. 2018). Astrochemical simulations for low-metallicity hot cores suggest that dust temperature during the initial ice-forming stage would play a key role in giving rise to the chemical diversity of organic molecules (Acharyya & Herbst 2018; Shimonishi et al. 2020). On the other hand, sulfur-bearing molecules such as SO2 and SO are commonly detected in known LMC hot cores, and their molecular abundances roughly scale with the metallicity of the LMC. Although the reason is still under debate, the results suggest that SO2 can be an alternative molecular species to trace hot-core chemistry in metal-poor environments.

The above results suggest that molecular abundances in hot cores do not always simply scale with the elemental abundances of their parent environments. However, it is still unclear if the observed chemical characteristics of LMC hot cores are common in other low-metallicity environments or they are uniquely seen only in the LMC. Currently, known low-metallicity hot-core samples are limited to those in the LMC. It is thus vital to understand the universal characteristics of interstellar chemistry by studying the chemical compositions of star-forming cores in diverse metallicity environments.

Recent surveys (e.g., Anderson et al. 2015, 2018; Izumi et al.2017; Wenger et al. 2021) have found a number of (∼10–20) star-forming region candidates in the extreme outer Galaxy, which is defined as having a galactocentric distance (DGC) larger than 18 kpc (Yasui et al. 2006; Kobayashi et al. 2008). The extreme outer Galaxy has a very different environment from those in the solar neighborhood, with lower metallicity (less than −0.5 dex, Fernández-Martín et al. 2017; Wenger et al. 2019), lower gas density (e.g., Nakanishi & Sofue 2016), and small or no perturbation from spiral arms. Such an environment is of great interest for studies of the star formation and ISM in the early phase of the Milky Way formation and those in dwarf galaxies (Ferguson et al. 1998; Kobayashi et al. 2008). The low-metallicity environment is in common with the Magellanic Clouds, and thus the extreme outer Galaxy is an ideal laboratory to test the universality of the low-metallicity molecular chemistry observed in the LMC and SMC.

Among star-forming regions in the extreme outer Galaxy, WB 89–789 (IRAS 06145+1455; 06h17m24fs2, 14°54'42'', J2000) has a particularly young and active nature (Brand & Wouterloot 1994). It is located at the galactocentric distance of 19.0 kpc, and its distance from Earth is 10.7 kpc (based on optical spectroscopy of a K3 III star; Brand & Wouterloot 2007). The metallicity of WB 89–789 is estimated to be a factor of 4 lower than the solar value according to the Galactic oxygen abundance gradient reported in the literature (Fernández-Martín et al. 2017; Bragança et al. 2019; Wenger et al. 2019; Arellano-Córdova et al. 2020, 2021). The region is associated with dense clouds traced by CS and CO (Brand & Wouterloot 2007). The total mass of the cloud is estimated to be 6 × 103 M for a ∼10 pc diameter area (Brand & Wouterloot 1994). An H2O maser is detected toward the region (Wouterloot et al. 1993), but no centimeter radio continuum is found (Brand & Wouterloot 2007). Several Class I protostar candidates were identified by previous infrared observations (Brand & Wouterloot 2007).

We here report the first detection of a hot molecular core in the extreme outer Galaxy based on submillimeter observations toward WB 89–789 with ALMA. Section 2 describes the details of the target source, observations, and data reduction. The observed molecular line spectra and images, as well as analyses of physical and chemical properties of the source, are presented in Section 3. A discussion about the properties of the hot core and comparisons of molecular abundances with known Galactic and LMC hot cores is given in Section 4. This section also presents the detection of another embedded protostar with high-velocity outflows in the WB 89–789 region. The conclusions are given in Section 5.

2. Target, Observations, and Data Reduction

2.1. Target

The target star-forming region is WB 89–789 (Brand & Wouterloot 1994). The region contains three Class I protostar candidates identified by near-infrared observations (Brand & Wouterloot 2007), and one of them is a main target of the present ALMA observations. The region observed with ALMA is indicated on a near-infrared two-color image shown in Figure 1. The observed position is notably reddened compared with other parts of WB 89–789.

Figure 1.

Figure 1. Near-infrared two-color image of the WB 89–789 star-forming region based on 2MASS data (Skrutskie et al. 2006). Blue is the J band (1.25 μm), and red is the Ks band (2.16 μm). The image size is 100'' × 100''. The green square indicates the field of view of the ALMA submillimeter images shown in Figures 45.

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2.2. Observations

Observations were conducted with ALMA in 2018 and 2019 as part of the Cycle 5 (2017.1.01002.S) and Cycle 6 (2018.1.00627.S) programs (PI: T. Shimonishi). A summary of the present observations is shown in Table 1. The pointing center of the antennas is R.A. = 06h17m23s and decl. = 14°54'41'' (ICRS). The total on-source integration time is 115.5 minutes for Band 6 data and 64.1 minutes for Band 7. Flux and bandpass calibrators are J0510+1800, J0854+2006, and J0725–0054 for Band 6, and J0854+2006 and J0510+1800 for Band 7. Phase calibrators are J0631+2020 and J0613+1708 for Band 6 and J0643+0857 and J0359+1433 for Band 7. Four spectral windows are used to cover the sky frequencies of 241.40–243.31, 243.76–245.66, 256.90–258.81, and 258.76–260.66 GHz for Band 6, ad 337.22–339.15, 339.03–340.96, 349.12–351.05, and 350.92–352.85 GHz for Band 7. The channel spacing is 0.98 MHz, which corresponds to 1.2 km s−1 for Band 6 and 0.85 km s−1 for Band 7. The total number of antennas is 45–49 for Band 6 and 43–44 for Band 7. The minimum–maximum baseline lengths are 15.1–783.5 m for Band 6 and 15.1–500.2 m for Band 7. The FWHM of the primary beam is about 25'' for Band 6 and 18'' for Band 7.

Table 1. Observation Summary

 ObservationOn-sourceMeanNumberBaseline  Channel
 DateTimePWV a ofMinMaxBeam size b MRS c Spacing
  (min)(mm)Antennas(m)(m)('' × '')('') 
Band 62018 Dec 6—115.50.5–1.545–4915.1783.50.41 × 0.505.60.98 MHz
(250 GHz)2019 Apr 16       (1.2 km s−1)
Band 72018 Apr 30—64.10.6–1.043–4415.1500.20.46 × 0.525.40.98 MHz
(350 GHz)2018 Aug 22       (0.85 km s−1)

Notes.

a Precipitable water vapor. b The average beam size of the continuum achieved by TCLEAN with Briggs weighting and the robustness parameter of 0.5. Note that we use a common circular restoring beam size of 0farcs50 for Band 6 and 7 data to construct the final images. c Maximum recoverable scale.

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2.3. Data Reduction

Raw data are processed with the Common Astronomy Software Applications (CASA) package. We use CASA 5.4.0 (Band 6) and 5.1.1 (Band 7) for the calibration and CASA 5.5.0 for the imaging. The synthesized beam sizes of 0farcs39–0farcs42 × 0farcs49–0farcs52 with a position angle of −36° for Band 6 and 0farcs45–0farcs46 × 0farcs51–0farcs52 with a position angle of −54° for Band 7 are achieved with Briggs weighting and a robustness parameter of 0.5. In this paper, we use a common circular restoring beam size of 0farcs50, which corresponds to 0.026 pc (5350 au) at the distance of WB 89–789. The synthesized images are corrected for the primary beam pattern using the impbcor task in CASA. The continuum image is constructed by selecting line-free channels. Before the spectral extraction, the continuum emission is subtracted from the spectral data using the CASA's uvcontsub task.

The spectra and continuum flux are extracted from the 0farcs50 diameter circular region centered at R.A. = 06h17m24fs073 and decl. = 14°54'42farcs27 (ICRS), which corresponds to the submillimeter continuum center of the target and is equivalent to the hot-core position. Hereafter, the source is referred to as WB 89–789 SMM1.

3. Results and Analysis

3.1. Spectra

Figures 23 show submillimeter spectra extracted from the continuum center of WB 89–789 SMM1. Spectral lines are identified with the aid of the Cologne Database for Molecular Spectroscopy 6 (CDMS; Müller et al. 2001, 2005) and the molecular database of the Jet Propulsion Laboratory 7 (JPL; Pickett et al. 1998). The detection criterion adopted here is the 3σ significance level and the velocity coincidence with the systemic velocity (Vsys) of WB 89–789 SMM1 (34.5 km s−1). The lines with a significance level higher than 2.5σ but lower than 3σ are indicated as tentative detection in the tables in Appendix A. More than 85% of lines are detected above the 5σ level.

Figure 2.

Figure 2. ALMA band 6 spectra extracted from the 0farcs50 (0.026 pc) diameter region centered at the present hot molecular core in the extreme outer Galaxy, WB 89–789 SMM1. Detected emission lines are labeled. Unidentified lines are indicated by "?". The source velocity of 34.5 km s−1 is assumed.

Standard image High-resolution image
Figure 3.

Figure 3. Same as in Figure 2, but for ALMA Band 7.

Standard image High-resolution image

Line parameters are measured by fitting a Gaussian profile to detected lines. We estimate the peak brightness temperature, the FWHM, the LSR velocity, and the integrated intensity for each line based on the fitting. For spectral lines for which a Gaussian profile does not fit well, their integrated intensities are calculated by directly integrating the spectrum over the frequency region of emission. Full details of the line fitting can be found in Appendix A (tables of measured line parameters) and Appendix B (figures of fitted spectra). The table also contains the estimated upper limits on important nondetection lines.

A variety of carbon-, oxygen-, nitrogen-, sulfur-, and silicon-bearing species, including COMs containing up to nine atoms, are detected from WB 89–789 SMM1 (see Table 2). Multiple high-excitation lines (upper state energy >100 K) are detected for many species. Measured line widths are typically 3–6 km s−1. Most of the lines consist of a single velocity component, but SiO has Doppler-shifted components at Vsys ± 5 km s−1 as indicated in Figure B1 in Appendix B.

Table 2. Summary of Detected Molecular Species

2 atoms3 atoms4 atoms5 atoms6 atoms7 atoms8 atoms9 atoms
CNHDOH2COc-C3H2 CH3OHCH3CHOHCOOCH3 CH3OCH3
NOH13CO+ HDCOHC3N 13CH3OHc-C2H4O C2H5OH
CSHC18O+ D2COH2CCOCH2DOH  C2H5CN
C34SH13CNHNCOHCOOHCH3CN   
C33SHC15NH2CS NH2CHO   
SOCCH      
34SOSO2       
33SO 34SO2       
SiOOCS      
  13OCS      

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3.2. Images

Figures 45 show synthesized images of continuum and molecular emission lines observed toward the target region. The images are constructed by integrating spectral data in the velocity range where the emission is detected. Most molecular lines, except for those of the molecular radicals CN, CCH, and NO, have their intensity peak at the continuum center, which corresponds to the position of a hot core. Simple molecules such as H13CO+, H13CN, CS, and SO are extended compared to the beam size. Secondary intensity peaks are also seen in those species. Complex molecules and HDO are concentrated at the hot-core position. A characteristic symmetric distribution is seen in SiO. Further discussion about the distribution of the observed emission is presented in Section 4.2.

Figure 4.

Figure 4. Integrated intensity distributions of molecular emission lines. Gray contours represent the 1.2 mm continuum distribution and the contour levels are 5σ, 10σ, 20σ, 40σ, and 100σ of the rms noise (0.044 mJy beam−1). Low signal-to-noise ratio regions (S/N < 2) are masked. The spectra discussed in the text are extracted from the region indicated by the black open circle. The blue cross represents the 1.2 mm continuum center. The synthesized beam size is shown by the gray filled circle in each panel. North is up, and east is to the left.

Standard image High-resolution image
Figure 5.

Figure 5. Same as in Figure 4.

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3.3. Derivation of Column Densities, Gas Temperatures, and Molecular Abundances

3.3.1. Rotation Diagram Analysis

Column densities and rotation temperatures are estimated based on the rotation diagram analysis for the molecular species where multiple transitions with different excitation energies are detected (Figure 6). We here assume an optically thin condition and the local thermodynamic equilibrium (LTE). We use the following formulae based on the standard treatment of the rotation diagram analysis (e.g., Sutton et al. 1995; Goldsmith & Langer 1999):

Equation (1)

where

Equation (2)

and Nu is a column density of molecules in the upper energy level, gu is the degeneracy of the upper level, k is the Boltzmann constant, ∫Tb dV is the integrated intensity estimated from the observations, ν is the transition frequency, S is the line strength, μ is the dipole moment, Trot is the rotational temperature, Eu is the upper state energy, N is the total column density, and Q(Trot) is the partition function at Trot. All of the spectroscopic parameters required in the analysis are extracted from the CDMS or JPL database. Derived column densities and rotation temperatures are summarized in Table 3.

Figure 6.

Figure 6. Results of rotation diagram analyses. Upper-limit points are shown by the downward arrows. The solid lines represent the fitted straight line. Derived column densities and rotation temperatures are shown in each panel. The open squares are excluded in the fit because they significantly deviate from other data points. The gray squares are also excluded in the fit because of their large S μ2 values. CH3OH is fitted using only E-type transitions, which are shown in blue. For HCOOH, trans- (square) and cis- (circle) species are plotted together. See Section 3.3.1 for details.

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Table 3. Estimated Rotation Temperatures, Column Densities, and Source Sizes

Molecule Trot N(X) N(X) Non-LTESize
 (K)(cm−2)(cm−2)('')
H2 1.1 × 1024 0.85 c
H13CO+ 35(7.0 ± 0.1) × 1012 (7.6 ± 0.9) × 1012 >1.5 d
HC18O+ 35(5.8 ± 0.9) × 1011 (5.7 ± 0.6) × 1011 1.18 d
CCH35(2.7 ± 0.1) × 1014 >2 d
c-C3H2 35(9.5 ± 2.2) × 1013 (8.2 ± 0.9) × 1013 a >1 d
H2CO39(1.1 ± 0.1) × 1014 (1.3 ± 0.1) × 1014 a >1.5 d
HDCO39(5.1 ± 0.3) × 1013 >1 d
D2CO ${{39}}_{-5}^{+6}$ (2.3 ± 0.5) × 1013 ⋯ ⋯>1 d
CN35(3.3 ± 0.2) × 1014 (2.5 ± 0.3) × 1014 >2 d
H13CN35(1.2 ± 0.1) × 1013 (1.1 ± 0.1) × 1013 0.92 d
HC15N35(6.3 ± 0.2) × 1012 (5.8 ± 0.6) × 1012 0.75 d
HC3N200(2.7 ± 0.3) × 1013 (2.1 ± 0.2) × 1013 0.65
NO35(9.0 ± 2.5) × 1014 (8.9 ± 0.9) × 1014 >1.5 d
HNCO ${{237}}_{-15}^{+17}$ (3.0 ± 0.2) × 1014 0.54
CH3CN ${{279}}_{-11}^{+12}$ (1.8 ± 0.1) × 1014 (8.6 ± 0.8) × 1013 0.51
13CH3CN200<5 × 1012
C2H5CN ${{130}}_{-15}^{+20}$ (6.3 ± 1.7) × 1013 0.52
NH2CHO ${{140}}_{-7}^{+8}$ (4.2 ± 0.7) × 1013 0.56
SiO35(2.5 ± 0.2) × 1012 (2.5 ± 0.3) × 1012 0.65
CS36(1.5 ± 0.2) × 1014 (2.0 ± 0.3) × 1014 >1.5
C34S36(3.1 ± 0.1) × 1013 0.70
C33S ${{36}}_{-3}^{+4}$ (1.5 ± 0.2) × 1013 0.61
OCS ${{106}}_{-5}^{+6}$ (6.5 ± 0.5) × 1014 (6.4 ± 0.7) × 1014 0.55
13OCS200(8.7 ± 2.4) × 1013 0.45
H2CS ${{43}}_{-2}^{+3}$ (1.5 ± 0.1) × 1014 (1.4 ± 0.2) × 1014 a 0.62
SO ${{35}}_{-1}^{+1}$ (4.0 ± 0.3) × 1014 (4.5 ± 0.5) × 1014 0.70 d
34SO35(5.9 ± 0.1) × 1013 0.66
33SO35(1.1 ± 0.1) × 1013 0.53
SO2 ${{166}}_{-5}^{+5}$ (1.2 ± 0.1) × 1015 0.53
34SO2 166(5.9 ± 0.9) × 1013 0.51
CH3SH200<3 × 1014
HDO ${{217}}_{-12}^{+14}$ (2.2 ± 0.2) × 1015 0.52
CH3OH ${{245}}_{-4}^{+4}$ (1.9 ± 0.1) × 1016 (2.6 ± 0.1) × 1016 b 0.51
13CH3OH ${{181}}_{-9}^{+10}$ (2.8 ± 0.2) × 1015 0.46
CH2DOH ${{155}}_{-15}^{+18}$ (4.6 ± 0.3) × 1015 0.52
HCOOCH3 ${{181}}_{-5}^{+6}$ (8.6 ± 0.4) × 1015 0.51
CH3OCH3 ${{137}}_{-4}^{+5}$ (2.6 ± 0.1) × 1015 0.52
C2H5OH ${{136}}_{-12}^{+14}$ (9.6 ± 1.3) × 1014 0.50
CH3CHO ${{192}}_{-34}^{+52}$ (6.4 ± 0.8) × 1014 0.49
trans-HCOOH ${{71}}_{-9}^{+11}$ (2.7 ± 0.6) × 1014 0.58
cis-HCOOH ${{69}}_{-21}^{+50}$ (2.4 ± 1.2) × 1013 0.49
H2CCO ${{92}}_{-11}^{+14}$ (1.0 ± 0.2) × 1014 0.55
c-C2H4O200(8.9 ± 2.0) × 1013 0.47

Notes. For Trot and N(X), those derived from rotation diagrams are shown in italics. Uncertainties and upper limits are of the 2σ level and do not include systematic errors due to adopted spectroscopic constants. See Sections 3.3.13.3.3 and 4.2 for details.

a Assuming ortho/para ratio of 3. b Assuming E-CH3OH/A-CH3OH ratio of unity (Wirström et al. 2011). c Size of continuum emission. d Associated with the extended component.

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Most molecular species are well fitted by a single temperature component. Data points in diagrams of CH3CN and C2H5CN are relatively scattered. For CH3OH, CH3CN, HNCO, SO2, and HCOOCH3, transitions with relatively large S μ2 values at low Eu (<300 K) are excluded from the fit in order to avoid the possible effect of optical thickness (see gray points in Figure 6). Adapted threshold values are log S μ2 > 1.1 for CH3OH, log S μ2 > 2.4 for CH3CN, log S μ2 > 1.6 for HNCO, log S μ2 > 1.2 for SO2, and log S μ2 > 1.8 for HCOOCH3.

Complex organic molecules, HDO, and SO2 show high rotation temperatures (>130 K). This suggests that they originate from a warm region associated with a protostar. On the other hand, C33S and D2CO, and H2CS show lower temperatures, suggesting that they arise from a colder region in the outer part of the protostellar envelope. SO also shows a low rotation temperature. Its Trot is close to that of C33S. However, SO lines are often optically thick in dense cores, particularly for low-Eu lines, thus the derived rotation temperature would be an upper limit.

3.3.2. Column Densities of Other Molecules

Column densities of molecular species for which rotation diagram analysis is not applicable are estimated from Equation (1) after solving it for N. Their rotation temperatures are estimated as follows, by taking into account that the sight line of WB 89–789 SMM1 contains both cold and warm gas components as described in Section 3.3.1.

The rotation temperature of C33S is applied to those of CS and C34S, considering a similar distribution of isotopologues. Similarly, the rotation temperature of D2CO is applied to H2CO and HDCO, and to that of SO2 to 34SO2. For other species, we assume that molecules with an extended spatial distribution trace a relatively low-temperature region rather than a high-temperature gas associated with a hot core. CN, CCH, H13CO+, HC18O+, H13CN, HC15N, NO, SiO, 34SO, 33SO, and c-C3H2 correspond to this case. We assume a rotation temperature of 35 K for those species, which is roughly equivalent to that of C33S.

High gas temperatures are observed for COMs, SO2, and HDO, which are associated with a compact hot-core region. The average temperature of those species is ∼200 K. We assume this temperature for column density estimates (including upper limit) of c-C2H4O, HC3N, 13CH3CN, 13OCS, and CH3SH. Estimated column densities are summarized in Table 3.

We have also estimated column densities of selected species based on non-LTE calculations with RADEX (van der Tak et al. 2007). For input parameters, we use the H2 gas density of 2.1 × 107 cm−3 according to our estimate in Section 3.3.3 and the background temperature of 2.73 K. Kinetic temperatures are assumed to be the same as temperatures tabulated in Table 3. The line intensities and widths are taken from the tables in Appendix A. 8 We assume an empirical 10% uncertainty for input line intensities. The resultant column densities are summarized in Table 3. The calculated non-LTE column densities are reasonably consistent with the LTE estimates.

3.3.3. Column Density of H2, Dust Extinction, and Gas Mass

A column density of molecular hydrogen (${N}_{{{\rm{H}}}_{2}}$) is estimated from the dust continuum data. We use the following equation to calculate ${N}_{{{\rm{H}}}_{2}}$ based on the standard treatment of optically thin dust emission:

Equation (3)

where Fν /Ω is the continuum flux density per beam solid angle as estimated from the observations, κν is the mass absorption coefficient of dust grains coated by thin ice mantles at 1200/870 μm as taken from Ossenkopf & Henning (1994), and we here use 1.07 cm2 g−1 for 1200 μm and 1.90 cm2 g−1 for 870 μm, Td is the dust temperature and Bν (Td ) is the Planck function, Z is the dust-to-gas mass ratio, μ is the mean atomic mass per hydrogen (1.41, according to Cox 2000), and mH is the hydrogen mass. We use the dust-to-gas mass ratio of 0.002, which is obtained by scaling the Galactic value of 0.008 by the metallicity of the WB 89–789 region.

A line of sight toward a hot core contains dust grains with different temperatures because of the temperature gradient in a protostellar envelope. Representative dust temperatures (i.e., mass-weighted average temperature) would fall somewhere in between that of a warm inner region and a cold outer region. Shimonishi et al. (2020) presented a detailed analysis of effective dust temperature in the sight line of a low-metallicity hot core in the LMC, based on a comparison of ${N}_{{{\rm{H}}}_{2}}$ derived by submillimeter dust continuum with the above method, model fitting of spectral energy distributions (SEDs), and the 9.7 μm silicate dust absorption depth. The paper concluded that Td = 60 K for the dust continuum analysis yields an ${N}_{{{\rm{H}}}_{2}}$ value that is consistent with those obtained by other different methods. This temperature corresponds to an intermediate value between a cold gas component (∼50 K) represented by SO and a warm component (∼150 K) represented by CH3OH and SO2 in this LMC hot core. The present hot core, WB 89–789 SMM1, harbors similar temperature components as discussed in Sections 3.3.1 and 3.3.2. We thus applied Td = 60 K for the present source. The continuum brightness of SMM1 is measured to be 11.33 ± 0.05 mJy beam−1 for 1200 μm and 28.0 ± 0.2 mJy beam−1 for 870 μm (3σ uncertainty). Based on the above assumption, we obtain ${N}_{{{\rm{H}}}_{2}}=1.6\times {10}^{24}$ cm−2 for 1200 μm and ${N}_{{{\rm{H}}}_{2}}=1.2\times {10}^{24}$ cm−2 for the 870 μm. The ${N}_{{{\rm{H}}}_{2}}$ value changes by a factor of up to 1.6 when the assumed Td is varied between 40 and 90 K.

Alternatively, a column density of molecular hydrogen can be determined by the model fitting of the observed SED. The best-fit SED discussed in Section 4.1 yields AV = 184 mag. We here use a standard value of NH/E(BV) = 5.8 × 1021 cm−2 mag−1 (Draine 2003) and a slightly high AV /E(BV) ratio of 4 for dense clouds (Whittet et al. 2001). Taking into account a factor of 4 lower metallicity, we obtain ${N}_{{{\rm{H}}}_{2}}$/AV = 2.9 × 1021 cm−2 mag−1, where we assume that all the hydrogen atoms are in the form of H2. Using this conversion factor, we obtain ${N}_{{{\rm{H}}}_{2}}=5.3\times {10}^{23}$ cm−2. This ${N}_{{{\rm{H}}}_{2}}$ is similar to the ${N}_{{{\rm{H}}}_{2}}$ derived from the aforementioned method assuming Td = 150 K. Such Td may be somewhat high as a typical dust temperature in the line of sight, but it is not a very unrealistic value given the observed temperature range of molecular gas toward WB 89–789 SMM1.

In this paper, we use ${N}_{{{\rm{H}}}_{2}}=1.1\times {10}^{24}$ cm−2 as a representative value, which corresponds to the average of ${N}_{{{\rm{H}}}_{2}}$ derived by the dust continuum data and the SED fitting. This ${N}_{{{\rm{H}}}_{2}}$ corresponds to AV = 380 mag using the above conversion factor. Assuming the source diameter of 0.026 pc and a uniform spherical distribution of gas around a protostar, we estimate the gas number density to be ${n}_{{{\rm{H}}}_{2}}=2.1\times {10}^{7}$ cm−3, where the total gas mass of 13 M is enclosed. Similarly, the mass for a 0.1 pc diameter region (i.e., a canonical size of dense cores) is estimated to be 75 M with Td = 60 K, where Band 6 and Band 7 estimates are averaged. For the whole field shown in Figures 45, which roughly corresponds to a 0.5 pc diameter region, the total mass is estimated to be 800–2500 M, where we assume Td = 20–10 K for extended dust emission. Note that this is a lower limit because the maximum recoverable scale of the present observations is 5farcs4 (0.28 pc).

3.3.4. Fractional Abundances and Isotope Abundance Ratios

Fractional abundances with respect to H2 are shown in Table 4, which are calculated based on column densities estimated in Sections 3.3.13.3.3. The fractional abundances normalized by the CH3OH column density are also discussed in Sections 4.34.4 because of the nonnegligible uncertainty associated with ${N}_{{{\rm{H}}}_{2}}$ (see Section 3.3.3).

Table 4. Estimated Fractional Abundances

Molecule N(X)/${N}_{{{\rm{H}}}_{2}}$
 0.026 pc area0.1 pc area
HCO+ a (9.5 ± 3.2) × 10−10 (1.5 ± 0.3) × 10−9
H2CO(1.0 ± 0.3) × 10−10 (1.2 ± 0.1) × 10−10
HDCO(4.7 ± 1.3) × 10−11 (3.9 ± 0.2) × 10−11
D2CO(2.1 ± 0.7) × 10−11 (2.0 ± 0.3) × 10−11
C2H(2.5 ± 0.7) × 10−10 (5.8 ± 1.2) × 10−10
c-C3H2 (8.6 ± 3.1) × 10−11 (5.9 ± 1.2) × 10−11
CN(3.0 ± 0.8) × 10−10 (6.6 ± 1.3) × 10−10
HCN a (1.7 ± 0.6) × 10−9 (1.2 ± 0.3) × 10−9
HC3N(2.5 ± 0.7) × 10−11 (1.4 ± 0.1) × 10−11
NO(8.1 ± 3.2) × 10−10 (1.6 ± 0.1) × 10−9
HNCO(2.7 ± 0.8) × 10−10 (7.1 ± 0.6) × 10−11
CH3CN b (4.2 ± 2.7) × 10−10 (3.7 ± 2.8) × 10−10
C2H5CN(5.8 ± 2.2) × 10−11 (2.4 ± 0.9) × 10−11
NH2CHO(3.8 ± 1.2) × 10−11 (1.8 ± 0.1) × 10−11
SiO(2.2 ± 0.6) × 10−12 (1.2 ± 0.1) × 10−12
CS c (9.7 ± 3.3) × 10−10 (6.4 ± 1.3) × 10−10
SO c (1.9 ± 0.5) × 10−9 (1.3 ± 0.3) × 10−9
OCS a (1.2 ± 0.5) × 10−8 (4.1 ± 1.4) × 10−9
H2CS(1.4 ± 0.4) × 10−10 (9.0 ± 1.0) × 10−11
SO2 (1.1 ± 0.3) × 10−9 (2.9 ± 0.1) × 10−10
CH3SH<3 × 10−10 <2 × 10−10
HDO(2.0 ± 0.6) × 10−9 (7.7 ± 0.9) × 10−10
CH3OH a (3.8 ± 1.3) × 10−7 (1.7 ± 0.3) × 10−7
CH2DOH(4.2 ± 1.2) × 10−9 (1.5 ± 0.2) × 10−9
HCOOCH3 (7.8 ± 2.2) × 10−9 (3.0 ± 0.2) × 10−9
CH3OCH3 (2.3 ± 0.6) × 10−9 (1.0 ± 0.1) × 10−9
C2H5OH(8.7 ± 2.7) × 10−10 (3.3 ± 0.8) × 10−10
CH3CHO(5.8 ± 1.8) × 10−10 (2.1 ± 0.4) × 10−10
HCOOH d (2.7 ± 1.0) × 10−10 (1.2 ± 0.4) × 10−10
H2CCO(9.2 ± 3.0) × 10−11 (3.7 ± 0.9) × 10−11
c-C2H4O(8.1 ± 2.8) × 10−11 (5.9 ± 1.2) × 10−11

Notes. Uncertainties and upper limits are of the 2σ level. Column densities of molecules for a 0.026 pc area are summarized in Table 3. An empirical uncertainty of 30% is assumed for ${N}_{{{\rm{H}}}_{2}}$.

a Estimated from the 13C isotopologue with 12C/13C = 150. b Rotation diagram analysis of CH3CN is used to derive a lower limit and the nondetection of 13CH3CN for an upper limit. c Estimated from the 34S isotopologue with 32S/34S = 35. d Sum of trans- and cis- species.

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Abundances of HCO+, HCN, SO, CS, OCS, and CH3OH are estimated from their isotopologues, H13CO+, H13CN, 34SO, C34S, O13CS, and 13CH3OH. Detections of isotopologue species for SO, CS, OCS, and CH3OH imply that the main species would be optically thick. Isotope abundance ratios of 12C/13C = 150 and 32S/33S = 35 are assumed, which are obtained by extrapolating the relationship between isotope ratios and galactocentric distances reported in Wilson & Rood (1994) and Humire et al. (2020) to DGC = 19 kpc.

Abundance ratios are derived for several rare isotopologues; we obtain CH2DOH/CH3OH = 0.011 ± 0.002, D2CO/HDCO = 0.45 ± 0.10, 34SO/33SO =5 ± 1, C34S/C33S = 2 ± 1, and 32SO2/34SO2 = 20 ± 4. The 32SO2/34SO2 ratio in WB 89–789 SMM1 is similar to the solar 32S/34S ratio (22, Wilson & Rood 1994), although we expect a slightly higher value in the outer Galaxy due to the 32S/34S gradient in the Galaxy (Chin et al. 1996; Humire et al. 2020). Astrophysical implications for the deuterated species are discussed in Section 4.4.

The rotation diagram of CH3CN is rather scattered. Although its isotopologue line is not detected, optical thickness might affect the column density estimate, as CH3CN is often optically thick in hot cores (e.g., Fuente et al. 2014). To obtain a possible range of its column density, we use the rotation diagram of 12CH3CN data to estimate a lower limit and the nondetection of the 13CH3CN(190–180) line at 339.36630 GHz (Eu = 163 K) for an upper limit.

We have also repeated the analysis for the spectra extracted from a 0.1 pc (1farcs93) diameter region at the hot-core position, for the sake of comparison with LMC hot cores (see Section 4.4). Those abundances are also summarized in Table 4. The abundances for a 0.1 pc area do not drastically vary from those for a 0.026 pc area. Molecules with a compact spatial distribution (e.g., COMs) tend to decrease their abundances by a factor of ∼2–3 in the 0.1 pc data due to the beam dilution effect. In contrast, those with extended spatial distributions and intensity peaks outside the hot-core region (H13CO+, CCH, CN, and NO) increase by a factor of ∼2 in the 0.1 pc data.

4. Discussion

4.1. Hot Molecular Core and Protostar Associated with WB 89–789 SMM1

The nature of WB 89–789 SMM1 is characterized by (i) the compact distribution of warm gas (∼0.03 pc, see Section 4.2), (ii) the high gas temperature that can trigger the ice sublimation (≥100 K, Section 3.3.1), (iii) the high density (2 × 107 cm−3, Section 3.3.3), (iv) the association with a luminous protostar (see below), and (v) the presence of chemically rich molecular gas. Those properties suggest that the source is associated with a hot molecular core.

Figure 7 shows an SED of SMM1, where the data are collected from available databases and literature (Brand & Wouterloot 2007; Wright et al. 2010; Yamamura et al. 2010). The bolometric luminosity of the source is estimated to be 8.4 × 103 L based on the SED fitting with the model of Robitaille et al. (2007). This luminosity is equivalent to a stellar mass of about 10 M according to the mass–luminosity relationship of zero-age main-sequence (ZAMS) stars (Zinnecker & Yorke 2007).

Figure 7.

Figure 7. The SED of WB 89–789 SMM1. The plotted data are obtained by the ESO 2.2 m telescope (pluses, black; Brand & Wouterloot 2007), the WISE all-sky survey (open diamonds, light green; Wright et al. 2010), AKARI FIS all-sky survey (open diamonds, blue; Yamamura et al. 2010), and ALMA (filled star, red, this work). The angular resolution of each data is indicated in brackets. The gray dashed line indicates the best-fitted SED with the model of Robitaille et al. (2007).

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Note that far-infrared data, which is important for the luminosity determination of embedded sources, is insufficient for SMM1. Only upper limits are provided due to the low angular resolution of available AKARI FIS all-sky survey data. Thus, the derived luminosity (and therefore mass) may be lower than the current estimate. Future high-spatial-resolution infrared observations in those missing wavelengths are highly required.

Alternatively, we can estimate the luminosity of SMM1 by scaling the luminosity of a low-metallicity LMC hot core, ST16, whose SED is well determined based on a comprehensive infrared data set from 1 to 1200 μm (Shimonishi et al. 2020). This LMC hot core has a total luminosity of 3.1 × 105 L and a Ks -band magnitude ([Ks ]) of 13.4 mag at 50 kpc, while SMM1 has [Ks ] = 14.7 mag at 10.7 kpc. Scaling the luminosity of ST16 with the distance and Ks -band magnitude, we obtain 4.3 × 103 L for SMM1, which is a factor of 2 lower than the estimate by the SED fitting. In either case, present estimates suggest that the luminosity of SMM1 would correspond to the lower end of high-mass ZAMS or upper end of intermediate-mass ZAMS.

4.2. Distribution of Molecular Line Emission and Dust Continuum

The observed emission lines and continuum show different spatial distributions depending on species. Those distributions have important clues to understand their origins. A schematic illustration of the temperature structure and molecular gas distribution in WB 89–789 SMM1 is shown in Figure 8 based on the discussion in this section.

Figure 8.

Figure 8. Schematic illustration of the molecular gas distribution and the temperature structure in WB 89–789 SMM1.

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We have estimated the spatial extent of the observed emission by fitting a two-dimensional Gaussian to the continuum center (Table 3). Compact distributions (FWHM =0farcs5–0farcs6, 0.026–0.031 pc), comparable with the beam size, are seen in HDO, COMs, CH3CN, HNCO, OCS, and high-excitation SO2 lines. HC3N is slightly extended (FWHM = 0farcs65). They are concentrated at the hot-core position, suggesting that they originate from a warm region where ice mantles are sublimated.

SO, 34SO, 33SO, and low-excitation SO2 show relatively compact distributions (FWHM = 0farcs5–0farcs7, 0.026–0.036 pc) at the hot-core position, but also show a secondary peak at the south side of the hot core. This secondary peak coincides with the peak of the NO emission. Other sulfur-bearing species such as C34S, C33S, and H2CS show compact distributions (FWHM = 0farcs6–0farcs0.7, 0.031–0.052 pc) centered at the hot core.

A characteristic distribution that is symmetric to the hot-core position is seen in SiO. It shows a compact emission (FWHM = 0farcs65) at the hot-core center, but also shows other peaks at the northeast and southwest sides of the hot core. Those secondary peaks are slightly elongated. SiO is a well-known shock tracer. The observed structure would have originated from the shocked gas produced by bipolar protostellar outflows. A driving source of the outflows would be a protostar embedded in a hot core as the distribution of SiO is symmetric with the hot-core position.

Even extended distributions (FWHM > 1farcs0) are seen in CN, CCH, H13CO+, HC18O+, H13CN, HC15N, NO, CS, H2CO, and HDCO, D2CO, and low-excitation CH3OH. Gas-phase reactions and nonthermal desorption of icy species would have a nonnegligible contribution to the formation of those species because they are widely distributed beyond the hot core. We note that dust continuum, H13CN, HC15N have a moderately sharp peak (FWHM < 1farcs0) at the hot-core position in addition to the extended component. c-C3H2 shows a patchy distribution, whose secondary peak at the southwest of the hot core does not coincide with those of other species.

Molecular radicals (CN, CCH, and NO) do not have their emission peak at the hot-core position. This would suggest that the chemistry outside the hot-core region largely contributes to their production. CN and CCH are known to be abundant in photodissociation regions (PDRs) because atomic carbon is efficiently provided by the photodissociation of CO under moderate UV fields (e.g., Fuente et al. 1993; Jansen et al. 1995; Sternberg & Dalgarno 1995; Rodriguez-Franco et al. 1998; Pety et al. 2017). In the present source, their emission shows a similar spatial distribution. A similar distribution between CN and CCH has been also observed in an LMC hot core by Shimonishi et al. (2020); they argue that CN and CCH would trace PDR-like outflow cavity structures that are irradiated by the UV light from a protostar associated with a hot core. We speculate that this is also the case for WB 89–789 SMM1.

Figure 9 shows the velocity maps (moment 1) of CN and CCH lines. CN and CCH emission are elongated in the southwest direction from the hot core (see also Figure 4). The figure also shows a possible direction of protostellar outflows expected from the spatial distribution of SiO. The elongated directions of CN and CCH coincide with the inferred direction of outflows. In addition, the elongated southwest parts of CN and CCH are blueshifted by ∼1–2 km s−1 compared to the hot-core position. This may be due to outflow gas motion, although CN and CCH would trace an outflow cavity wall rather than the outflow gas itself. Actually, the observed velocity shift is smaller than a typical value of high-velocity wing components in massive protostellar outflows (≥5 km s−1; e.g., Beuther et al.2002; Maud et al. 2015). We note that a clear velocity structure is not seen in the SiO velocity map, except for the position of another embedded protostar discussed in Section 4.5. Future observations of optically thick outflow tracers such as CO are necessary to confirm the presence of high-velocity gas associated with protostellar outflows.

Figure 9.

Figure 9. Velocity maps (moment 1) of CN and CCH lines. The color scale indicates the offset velocity relative to the systemic velocity of 34.5 km s−1. A possible direction of outflows expected from the distributions of SiO is shown by the red arrows. Contours represent the integrated intensity distribution, and the contour levels are 8%, 20%, 40%, and 60% of the peak value. Low signal-to-noise regions (S/N < 5) are masked. The blue cross represents the 1.2 mm continuum center.

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4.3. Molecular Abundances: Comparison with Galactic Hot Cores

Figure 10 shows a comparison of molecular abundances between WB 89–789 SMM1 and other known Galactic hot cores. The data for an intermediate-mass hot core, NGC 7192 FIRS2, are adopted from Fuente et al. (2014). The abundances are based on the 220 GHz region observations for a 0.009 pc diameter area centered at the hot core. The luminosity of NGC 7192 FIRS2 (∼500 L) corresponds to that of a 5 M ZAMS. The data for a high-mass source, the Orion hot core, are adopted from Sutton et al. (1995), based on the 340 GHz region observations for a 0.027 pc diameter area at the hot core. The abundance of HNCO is taken from Schutte & Greenberg (1997).

Figure 10.

Figure 10. Comparison of molecular abundances between an outer Galactic hot core (black, WB 89–789 SMM1), an intermediate-mass hot core (green, NGC 7192 FIRS2), and a high-mass hot core (cyan, Orion). An abundance difference by a factor of 4 is indicated by the black solid line with hats. The area with thin vertical lines indicates the error bar. No data are available for HDO in NGC 7192 FIRS2. See Section 4.3 for details.

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The molecular abundances in WB 89–789 SMM1 are generally lower than those of the inner Galactic counterparts. The degree of the abundance decrease is roughly consistent with the lower metallicity of the WB 89–789 region as indicated by the scale bar in Figure 10. Particularly, SMM1 and the intermediate-mass hot core NGC 7192 FIRS2 show similar molecular abundances after taking into account the four times lower metallicity of the former source. For the comparison with Orion, it seems that HC3N, C2H5CN, and SO2 are significantly less abundant in SMM1 even taking into account the lower metallicity, while CH3OH is overabundant in SMM1 despite the low metallicity.

To further focus on chemical complexity at low metallicity, Figure 11 shows a comparison of fractional abundances of COMs normalized by the CH3OH column density for WB 89–789 SMM1 and NGC 7192 FIRS2. Such a comparison is useful for investigating the chemistry of organic molecules in warm and dense gas around protostars (Herbst & van Dishoeck 2009; Drozdovskaya et al. 2019) because CH3OH is believed to be a parental molecule for the formation of even larger COMs (e.g., Nomura & Millar 2004; Garrod & Herbst 2006). In addition, CH3OH is a product of grain surface reaction, thus warm CH3OH gas mainly arises from a high-temperature region, where ices are sublimated and characteristic hot-core chemistry proceeds. Furthermore, the normalization by CH3OH can cancel the metallicity effect in the abundance comparison.

Figure 11.

Figure 11. Comparison of molecular abundances normalized by the CH3OH column density for (a) WB 89–789 SMM1 versus NGC 7192 FIRS2 and (b) WB 89–789 SMM1 versus ST16 (LMC). Carbon- and oxygen-bearing species are shown by the blue squares, nitrogen-bearing species in green, and sulfur-bearing species in red. The dotted lines in panel (a) represent an abundance ratio of 2:1 and 1:2 for WB 89–789 SMM1: NGC 7192 FIRS2, while the solid line represents that of the 1:1 ratio. Similarly, the dotted lines in panel (b) represent a ratio of 100:1, 10:1, 1:10, and 1:100 for WB 89–789 SMM1:ST16, while the solid line represents a 1:1 ratio. The leftward triangles in panel (b) indicate the upper limit for ST16. See Section 4.3 for details.

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The N(X)/N(CH3OH) ratios are remarkably similar between WB 89–789 SMM1 and NGC 7192 FIRS2 as shown in Figure 11(a). The ratios of SMM1 coincide with those of NGC 7192 FIRS2 within a factor of 2 for the most molecular species. The correlation coefficient is calculated to be 0.94, while it is 0.96 if CH3CN is excluded. It seems that CH3CN deviates from the overall trend, although the uncertainty is large due to the opacity effect (see 3.3.4). C2H5OH also slightly deviates from the trend. The reason for their behavior is still unclear, but it may be related to the formation pathway of those molecules.

The above two comparisons suggest that chemical compositions of the hot core in the extreme outer Galaxy scale with the metallicity. In the WB 89–789 region, the metallicity is expected to be four times lower compared to the solar neighborhood. The observed abundances of COMs in the SMM1 hot core are lower than the other Galactic hot cores, but the decrease is proportional to this metallicity. Furthermore, similar N(COMs)/N(CH3OH) ratios suggest that CH3OH is an important parental species for the formation of larger COMs in a hot core, as suggested by the aforementioned theoretical studies.

CH3OH ice is believed to form on grain surfaces, and several formation processes are proposed by laboratory experiments; i.e., hydrogenation of CO, ultraviolet photolysis, and radiolysis of ice mixtures (e.g., Hudson & Moore 1999; Watanabe et al. 2007). It is known that CH3OH is already formed in quiescent prestellar cores before star formation occurs (Boogert et al. 2011). Solid CH3OH will chemically evolve to larger COMs through a combination of photolysis, radiolysis, and grain heating during the warm-up phase that leads to the formation of a hot core (Garrod & Herbst 2006). High-temperature gas-phase chemistry of sublimated CH3OH would also contribute to the COM formation (Nomura & Millar 2004; Taquet et al. 2016). The present results suggest that various COMs can form even in a low-metallicity environment, if their parental molecule, CH3OH, is efficiently produced in a star-forming core. The detection of a chemically rich star-forming core in the extreme outer Galaxy has an impact on the understanding of the occurrence of the chemical complexity in a primordial environment of the early phase of the Galaxy formation. We here note that observations of ice mantle compositions have not been reported for the outer Galaxy so far. Future infrared observations of ice absorption bands toward embedded sources in the outer Galaxy are important.

4.4. Molecular Abundances: Comparison with LMC Hot Cores

It is still unknown if the observed simply metallicity-scaled chemistry of COMs in the WB 89–789 SMM1 hot core is common in other hot-core sources in the outer Galaxy. A comparison of the present data with those of hot cores in the LMC would provide a hint for understanding the universality of low-metallicity hot-core chemistry. The metallicity of the LMC is reported to be lower than the solar value by a factor of 2 to 3 (e.g., Dufour et al. 1982; Westerlund 1990; Russell & Dopita 1992; Choudhury et al. 2016), which is in common with the outer Galaxy.

Figure 12 shows a comparison of molecular abundances between WB 89–789 SMM1 and three LMC hot cores. The plotted molecular column densities for LMC hot cores are adopted from Shimonishi et al. (2016a) for ST11, Shimonishi et al. (2020) for ST16, and Sewiło et al. (2018) from N113 A1. Another LMC hot core in Sewiło et al. (2018), N113 B3, has similar molecular abundances to N113 A1. The ${N}_{{{\rm{H}}}_{2}}$ value of ST11 and N113 A1 is reestimated using the same dust opacity data and dust temperature (Td = 60 K) as in this work; we obtained ${N}_{{{\rm{H}}}_{2}}=1.2\times {10}^{24}$ cm−2 for ST11 and ${N}_{{{\rm{H}}}_{2}}\,=9.2\times {10}^{23}$ cm−2 for N113 A1. The dust temperature assumed in ST16 is 60 K as described in Section 3.3.3. Molecular column densities are estimated for circular/elliptical regions of 0.12 × 0.12 pc, 0.10 × 0.10 pc, and 0.21 × 0.13 pc for ST11, ST16, and N113 A1, respectively. For a fair comparison, we have recalculated ${N}_{{{\rm{H}}}_{2}}$ and molecular column densities of SMM1 for a 0.1 pc (1farcs93) diameter region. Those abundances are plotted in Figure 12 and summarized in Table 4.

Figure 12.

Figure 12. Comparison of molecular abundances between an outer Galactic hot core, WB 89–789 SMM1 (black), and three LMC hot cores, ST11 (red), ST16 (orange), and N113 A1 (light yellow). Abundances of SMM1 are calculated for a 0.1 pc diameter region. The area with the thin vertical lines indicates the error bar. The bar with a color gradient indicates an upper limit. The absence of bars indicates the lack of available data. See Section 4.4 for details.

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The chemical composition of the outer Galaxy hot core does not resemble those of LMC hot cores as seen in Figure 12. The dissimilarity is also seen in the N(X)/N(CH3OH) comparison between SMM1 and ST16 as shown in Figure 11(b), where the correlation coefficient is calculated to be 0.69.

Shimonishi et al. (2020) argue that SO2 will be a good tracer of low-metallicity hot-core chemistry because (i) it is commonly detected in LMC hot cores with similar abundances, and (ii) it originated from a compact hot-core region. SO also shows similar abundances within LMC hot cores. In WB 89–789 SMM1, however, the abundances of SO2 and SO relative to H2 are lower by a factor of 28 and 5 compared with LMC hot cores. The measured rotation temperatures of SO2 are similar between those hot cores, i.e., 166 K (SO2) for SMM1, 232 K (SO2) and 86 K (34SO2) for ST16, 190 K (SO2) and 95 K (34SO2) for ST11. The SO2 column densities for ST16 and ST11 are estimated from 34SO2, while that for SMM1 is from SO2. However, the SO2 column density of SMM1 increases only by a factor of up to 3 when it is estimated from 34SO2 (see Section 3.3.4). Thus, the low SO2 abundance in the outer Galactic hot core would not be due to the optical thickness.

In contrast to the S–O bond-bearing species, the C–S bond-bearing species such as CS, H2CS, and OCS do not show a significant abundance decrease in WB 89–789 SMM1. Thus, it is not straightforward to attribute the low abundance of SO2 (and perhaps SO) to the low elemental abundance ratio of sulfur in the outer Galaxy. Hot-core chemistry models suggest that SO2 is mainly produced in high-temperature gas-phase reactions in warm gas, using H2S sublimated from ice mantles (Charnley 1997; Nomura & Millar 2004). This also applies to the SO2 formation in low-metallicity sources as shown in astrochemical simulations for LMC hot cores (Shimonishi et al.2020). We speculate that the different behavior of SO2 in the outer Galaxy and LMC hot cores may be related to differences in the evolutionary stage of hot cores. A different luminosity of host protostars may also contribute to the different sulfur chemistry, i.e., ∼8 × 103 L for WB 89–789 SMM1, while several ×105 L for LMC hot cores. A different cosmic-ray ionization rate between the outer Galaxy and the LMC may also affect the chemical evolution, although the rate is not known for the outer Galaxy.

Among nitrogen-bearing molecules, NO shows interesting behavior in LMC hot cores. After correcting for the metallicity, NO is overabundant in LMC hot cores compared with Galactic counterparts despite the low elemental abundance of nitrogen in the LMC (Shimonishi et al. 2020). Only NO shows such behavior among the nitrogen-bearing molecules observed in LMC hot cores. In WB 89–789 SMM1, however, such an overabundance of NO is not observed. The NO abundance of SMM1 is 1.6 × 10−9 for a 0.1 pc region data. This is a factor of 5 lower than a typical NO abundance in Galactic high-mass hot cores (8×10−9, Ziurys et al. 1991), which is consistent with a factor of 4 lower metallicity in WB 89–789. The present high-spatial-resolution data have revealed that NO does not mainly arise from a hot-core region, as shown in Figure 4. It has an intensity peak at the south part of the hot core, where low-excitation lines of SO and SO2 also have a secondary peak (Section 4.2). Thus, shock chemistry or photochemistry, rather than high-temperature chemistry, would contribute to the production of NO in low-metallicity protostellar cores. In that case, a lower luminosity of SMM1 than those of LMC hot cores may contribute to the different behavior of NO.

For other nitrogen-bearing molecules, HNCO and CH3CN, a clear difference is not identified between outer Galactic and LMC hot cores, although the number of data points is limited and the abundance uncertainty is large. The reason for the unusually low abundance of SiO in SMM1 is unknown. It may be related to different shock conditions or grain compositions because dust sputtering by shock is mainly responsible for the production of SiO gas.

The formation of COMs is one of the important standpoints for low-metallicity hot-core chemistry. It is reported that CH3OH shows a large abundance variation in LMC hot cores (Shimonishi et al. 2020). There are organic-poor hot cores such as ST11 and ST16, while N113 A1 and B3 are organic rich. The CH3OH abundance of WB 89–789 SMM1 is higher than those of any known LMC hot cores. The abundances of HCOOCH3 and CH3OCH3 in SMM1 are comparable with those of an organic-rich LMC hot core, N113 A1. The detection of many other COMs in SMM1 suggests the source has experienced rich organic chemistry despite its low-metallicity nature.

Astrochemical simulations for LMC hot cores suggest that dust temperature at the initial ice-forming stage has a major effect on the abundance of CH3OH gas in the subsequent hot-core stage (Acharyya & Herbst 2018; Shimonishi et al. 2020). Simulations of grain surface chemistry dedicated to the LMC environment also suggest that dust temperature is one of the key parameters for the formation of CH3OH in dense cores (Acharyya & Herbst 2015; Pauly & Garrod 2018). This is because (i) CH3OH is mainly formed by the grain surface reaction, and (ii) the hydrogenation reaction of CO, which is a dominant pathway for the CH3OH formation, is sensitive to the dust temperature due to the high volatility of atomic hydrogen. For this reason, it is inferred that organic-rich hot cores had experienced a cold stage (≲10K) that is sufficient for CH3OH formation before the hot-core stage, while organic-poor ones might have missed such a condition for some reason. Alternatively, the slight difference in the hot core's evolutionary stage may contribute to the CH3OH abundance variation, because the high-temperature gas-phase chemistry is rapid, and it can decrease CH3OH gas at a late stage (e.g., Nomura & Millar 2004; Garrod & Herbst 2006; Vasyunin & Herbst 2013; Balucani et al. 2015).

Low-metallicity hot-core chemistry simulations in Shimonishi et al. (2020) argue that the maximum achievable abundances of CH3OH gas in a hot-core stage significantly decrease as the visual extinction of the initial ice-forming stage decreases. On the other hand, the simulations show that the CH3OH gas abundance is simply metallicity scaled if the initial ice-forming stage is sufficiently shielded. In a well-shielded initial condition, the grain surface is cold enough to trigger CO hydrogenation, and the resultant CH3OH abundance is roughly regulated by the elemental abundances. The observed metallicity-scaled chemistry of COMs in WB 89–789 SMM1 implies that the source had experienced such an initial condition before the hot-core stage.

Deuterium chemistry is widely used in interpreting the chemical and physical history of interstellar molecules (e.g., Caselli & Ceccarelli 2012; Ceccarelli et al. 2014). The measured CH2DOH/CH3OH ratio in WB 89–789 SMM1 is 1.1% ± 0.2%, which is comparable to the higher end of those ratios observed in high-mass protostars and the lower end of those in low-mass protostars (e.g., see Figure 2 in Drozdovskaya et al. 2021). The ratio is orders of magnitude higher than the deuterium-to-hydrogen ratio in the solar neighborhood (2×10−5; Linsky et al. 2006; Prodanović et al. 2010) and that in the big bang nucleosynthesis (3 × 10−5; Burles 2002 and references therein). This suggests that the efficient deuterium fractionation occurred upon the formation of CH3OH in SMM1. The D2CO/HDCO ratio is 45% ± 10%, which is comparable to those observed in low-mass and high-mass protostars (e.g., Zahorecz et al. 2021). This would suggest that physical conditions for deuterium fractionation could be similar between WB 89–789 SMM1 and inner Galactic protostars. Note that higher-spatial-resolution observations and detailed multiline analyses would affect the measured abundance of deuterated species as reported in Persson et al. (2018) for the case of a nearby low-mass protostar. The H2CO column density derived in this work may be a lower limit because the line is often optically thick, thus we do not discuss the abundance ratio relative to H2CO.

It is known that the deuterium fractionation efficiently proceeds at low temperature (e.g., Roberts et al. 2003; Caselli & Ceccarelli 2012; Taquet et al. 2014; Furuya et al. 2016). This is because the key reaction for the trigger of deuterium fractionation, ${{\rm{H}}}_{3}^{+}$ + HD → H2D+ + H2 + 232 K, is exothermic and its backward reaction cannot efficiently proceed below 20 K. In addition, gaseous neutral species such as CO and O efficiently destruct H2D+, thus their depletion at low temperature further enhances the deuterium fractionation (e.g., Caselli & Ceccarelli 2012). A sign of high deuterium fractionation observed in WB 89–789 SMM1 suggests that the source had experienced such a cold environment during its formation. This picture is consistent with the implication obtained from the metallicity-scaled chemistry of COMs, which also suggests the occurrence of a cold and well-shielded initial condition as discussed above.

Although the low metallicity is common between the outer Galaxy and the LMC, their star-forming environments would be different; the LMC has more harsh environments as inferred from active massive star formation over the whole galaxy, while that for the outer Galaxy might be quiescent due to its low star formation activity. Those environmental differences need to be taken into account for further understanding of the chemical evolution of star-forming regions at low metallicity. A future extensive survey of protostellar objects toward the outer Galaxy is thus vitally important for further discussion. Astrochemical simulations dedicated to the environment of the outer Galaxy, and the application to lower-mass protostars, are also important.

4.5. Another Embedded Protostar Traced by High-velocity SiO Gas

We have also detected a compact source associated with high-velocity SiO gas at the east side of WB 89–789 SMM1. Hereafter, we refer to this source as WB 89–789 SMM2. According to the SiO emission, the source is located at R.A. = 06h17m24fs246 and decl. = 14°54'43farcs25 (ICRS), which is 2farcs7 (0.14 pc) away from SMM2. Figure 13(a) shows the SiO(6–5) spectrum extracted from a 0farcs6 diameter region centered at the above position. The SiO line is largely shifted to the blue and red sides relative to the systemic velocity in a symmetric fashion. The peaks of the shifted emission are located at Vsys ± 25 km s−1.

Figure 13.

Figure 13. (a) SiO(6–5) spectrum of WB 89–789 SMM2. The dotted line indicates a systemic velocity of 34.5 km s−1. High-velocity (Vsys ± 25 km s−1) SiO components are seen at the blue-/redshifted sides of the systemic velocity. (b) Velocity map (moment 1) of the SiO(6–5) line. The color scale indicates the offset velocity relative to the systemic velocity. Low signal-to-noise ratio regions (S/N < 5) are masked. Gray contours represent the intensity distribution of SiO(6–5) integrated from 0 to 60 km s−1, and the contour levels are 1.5σ, 4σ, and 12σ of the rms level. The yellow star indicates the SiO center of SMM2, while the blue cross indicates the hot-core position (SMM1). The subset panel shows the 1200 μm continuum image for a 1farcs2 × 1farcs2 region centered at SMM2. See Section 4.5 for details.

Standard image High-resolution image

Figure 13(b) shows a velocity map and the integrated intensity distribution of SiO(6–5). In the figure, to focus on SiO in WB 89–789 SMM2, the intensity is integrated over a much wider velocity range (0–60 km s−1) compared with that adopted in Figure 4 (31–38 km s−1). The velocity map clearly indicates that the velocity structure of SiO in SMM2 is spatially symmetric to the SiO center. At this position, a local peak is seen in the 1200 μm continuum as shown in the figure, suggesting the presence of an embedded source. SMM2 does not show any emission lines of COMs, and no alternative molecular lines are identified at the frequencies of Doppler-shifted SiO emission. Also taking into account the clear spectral and spatial symmetry, the observed lines must be attributed to high-velocity SiO gas.

The spectral characteristics of the observed high-velocity SiO resemble those of extremely high-velocity (EHV) outflows observed in Class 0 protostars (Bachiller et al. 1991; Tafalla et al. 2010, 2015; Tychoniec et al. 2019). The EHV flows are known to appear as a discrete high-velocity (V ≳ 30 km s−1) peak and are observed in the youngest stage of star formation (Bachiller 1996; Matsushita et al. 2019 and references therein). The EHV flows extend up to several thousands of astronomical units from the central protostar in SiO and usually have collimated bipolar structures (e.g., Bachiller et al. 1991; Hirano et al. 2010; Matsushita et al. 2019; Tychoniec et al. 2019). The beam size of the present data is about 5000 au, thus such structures will not be fully spatially resolved. Actually, a symmetric spatial distribution of blue-/redshifted SiO is only marginally resolved into two beam size regions (Figure 13(b)). The spatial extent of SiO emission is about 1'' (0.052 pc). Assuming an outflow velocity of 25 km s−1, we estimate a dynamical timescale of EHV flows to be at least 2000 yr. This is roughly consistent with the dynamical timescales of other EHV sources, which range from a few hundred to a few thousand years (Bachiller 1996 and references therein).

A 1200 μm continuum flux in a 0farcs6 diameter region centered at SMM2 is 0.60 ± 0.05 mJy beam−1. Assuming Td = 20 K, we obtain ${N}_{{{\rm{H}}}_{2}}=3.2\times {10}^{23}$ cm−2. This is equivalent to a gas number density of ${n}_{{{\rm{H}}}_{2}}=4.9\times {10}^{6}$ cm−3. If we assume a higher Td , i.e., 40 K, then the derived column density is 2.5 times lower than the 20 K case. In either case, the continuum data suggest the presence of high-density gas at this position. A column density and fractional abundance of SiO gas at the above position is estimated to be N(SiO) ∼ 2 × 1013 cm−2 and N(SiO)/${N}_{{{\rm{H}}}_{2}}\sim 6\times {10}^{-11}$, where we assume optically thin emission in the LTE and the gas/dust temperature of 20 K. The fractional abundance will be two times higher if we assume the gas/dust temperature of 10 K or 40 K. The SiO abundance in SMM2 is at least 30 times higher than that observed in SMM1. The observed enhancement of SiO in SMM2 would be related to shock chemistry triggered by EHV outflows.

Previous single-dish observations of CO detected extended (∼20'') molecular outflows in the WB 89–789 region (Brand & Wouterloot 1994, 2007). The center of the outflow gas coincides with the position of the IRAS source (IRAS 06145+1455; 06h17m24fs2, 14°54'42'', J2000). This position is consistent with those of SMM1 or SMM2, given the large beam size of CO(3–2) observations (14'') in Brand & Wouterloot (2007). The observed CO outflow gas has an extended blueshifted component (20 < VLSR < 31 km s−1) toward the southeast direction from the center, while a redshifted component (37 < VLSR < 55 km s−1) is extended toward the northwest direction (see Figure 9 in Brand & Wouterloot 2007). This outflow direction coincides with that of the high-velocity SiO outflows observed in this work. The SiO outflows from SMM2 may have a common origin with the large-scale CO outflows.

In summary, it is likely that a compact, high-density, and embedded object is located at the position of WB 89–789 SMM2. Presumably, a protostar associated with SMM2 is driving the observed high-velocity SiO gas flows. Its short dynamical timescale and similarity to EHV flows suggest that the object is at the youngest stage of star formation (Class 0/I). Nondetection of warm gas emission also supports its young nature. We note that the detailed structure of high-velocity SiO gas is not fully spatially resolved, and CO lines, which often trace high-velocity outflows, are not covered in the present data. Future high-spatial-resolution observations of CO and other outflow tracers are key to further clarify the nature of WB 89–789 SMM2.

5. Summary

The extreme outer Galaxy is an excellent laboratory to study star formation and ISM in a Galactic low-metallicity environment. The following conclusions are obtained in this work.

  • 1.  
    A hot molecular core is for the first time detected in the extreme outer Galaxy (WB 89–789 SMM1), based on submillimeter observations with ALMA toward the WB 89–789 star-forming region located at the galactocentric distance of 19 kpc.
  • 2.  
    A variety of carbon-, oxygen-, nitrogen-, sulfur-, and silicon-bearing species, including COMs containing up to nine atoms and larger than CH3OH, are detected toward a warm (>100 K) and compact (<0.03 pc) region associated with a protostar (∼8 × 103 L). The results suggest that a great molecular complexity exists even in a lower-metallicity environment of the extreme outer Galaxy.
  • 3.  
    For deuterated species, we have detected HDO, HDCO, D2CO, and CH2DOH. HDO and CH2DOH arise from a compact and high-temperature (Trot = 155–220) region, while HDCO and D2CO are in a lower-temperature (Trot ∼ 40 K) and slightly extended region. The measured ratios of CH2DOH/CH3OH and D2CO/HDCO are 1.1% ± 0.2% and 45% ± 10%, respectively.
  • 4.  
    Fractional abundances of CH3OH and other COMs relative to H2 generally scale with the metallicity of WB 89–789, which is a factor of 4 lower than the solar value.
  • 5.  
    A comparison of fractional abundances of COMs relative to the CH3OH column density between the outer Galactic hot core and a Galactic intermediate-mass hot core shows a remarkable similarity. The results suggest a metallicity-scaled chemistry for the formation of COMs in this source. CH3OH is an important parental molecule for COMs formation even in a lower-metallicity environment.
  • 6.  
    On the other hand, the molecular abundances of the present hot core do not resemble those of LMC hot cores. We speculate that different luminosities or star-forming environments between outer Galactic and LMC hot cores may contribute to this.
  • 7.  
    According to astrochemical simulations of low-metallicity hot cores, the observed metallicity-scaled chemistry of COMs in WB 89–789 SMM1 implies that the source had experienced a well-shielded and cold ice-forming stage before the hot-core stage.
  • 8.  
    We have also detected another compact source (WB 89–789 SMM2) associated with high-velocity SiO gas (Vsys ± 25 km s−1) in the same region. The characteristics of the source resemble those of EHV outflows observed in Class 0 protostars. Physical properties and dynamical timescale of this outflow source are discussed.

This paper makes use of the following ALMA data: ADS/JAO.ALMA#2017.1.01002.S and 2018.1.00627.S. ALMA is a partnership of ESO (representing its member states), NSF (USA) and NINS (Japan), together with NRC (Canada), MOST and ASIAA (Taiwan), and KASI (Republic of Korea), in cooperation with the Republic of Chile. The Joint ALMA Observatory is operated by ESO, AUI/NRAO and NAOJ. This work has made extensive use of the Cologne Database for Molecular Spectroscopy and the molecular database of the Jet Propulsion Laboratory. This work makes use of data products from the Two Micron All Sky Survey, which is a joint project of the University of Massachusetts and the Infrared Processing and Analysis Center/California Institute of Technology, funded by the National Aeronautics and Space Administration and the National Science Foundation. This work was supported by JSPS KAKENHI grant Nos. 19H05067, 21H00037, and 21H01145. Finally, we would like to thank an anonymous referee for insightful comments, which substantially improved this paper.

Software: CASA (McMullin et al. 2007).

Appendix A: Measured Line Parameters

Tables A1A9 summarize the measured line parameters (see Section 3.1 for details). The tabulated uncertainties and upper limits are of 2σ level and do not include systematic errors due to continuum subtraction. Upper limits are estimated assuming ΔV = 4 km s−1.

Table A1. Line Parameters for HDO, H13CO+, HC18O+, CCH, c-C3H2, H2CO, HDCO, and D2CO

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
HDO21, 1–21, 2 95241.561550.99 ± 0.034.85.05 ± 0.2934.60.04
HDO73, 4–64, 3 837241.973570.28 ± 0.022.10.63 ± 0.1234.10.04
H13CO+ 3–225260.255345.85 ± 0.022.314.23 ± 0.1334.10.03
HC18O+ 4–341340.630690.64 ± 0.051.91.29 ± 0.2034.10.07
CCH N = 4–3, ${\text{}}J=\tfrac{9}{2}\mbox{--}\tfrac{7}{2}$, F = 5–442349.337714.39 ± 0.042.612.32 ± 0.2433.70.08(1)
CCH N = 4–3, ${\text{}}J=\tfrac{7}{2}\mbox{--}\tfrac{5}{2}$, F = 4–342349.399283.54 ± 0.042.810.49 ± 0.2633.70.08(1)
c-C3H2 32, 1–21, 2 18244.222150.23 ± 0.024.81.18 ± 0.2733.60.04
c-C3H2 53, 2–44, 1 45260.479750.09 ± 0.021.60.15 ± 0.1032.90.03(2)
H2CO51, 5–41, 4 62351.768647.02 ± 0.053.727.32 ± 0.4034.20.08
HDCO42, 3–32, 2 63257.748700.94 ± 0.022.82.80 ± 0.1434.30.03
HDCO42, 2–32, 1 63259.034910.97 ± 0.022.93.00 ± 0.1834.30.03
D2CO41, 3–31, 2 35245.532750.64 ± 0.032.31.54 ± 0.1534.20.04
D2CO62, 5–52, 4 80349.630610.76 ± 0.042.41.92 ± 0.2333.90.08

Note. (1) Blend of two hyperfine components. (2) Tentative detection.

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Table A2. Line Parameters for N-bearing Molecules

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
H13CN3–225259.011803.25 ± 0.024.214.45 ± 0.1934.30.03
HC15N3–225258.157001.95 ± 0.023.67.45 ± 0.1934.30.03
CN N = 3–2, ${\text{}}J=\tfrac{5}{2}\mbox{--}\tfrac{5}{2}$, ${\text{}}F=\tfrac{3}{2}\mbox{--}\tfrac{3}{2}$ 33339.446780.30 ± 0.042.60.82 ± 0.2234.60.07
CN N = 3–2, ${\text{}}J=\tfrac{5}{2}\mbox{--}\tfrac{5}{2}$, ${\text{}}F=\tfrac{5}{2}\mbox{--}\tfrac{5}{2}$ 33339.475900.39 ± 0.041.70.71 ± 0.1734.00.07
CN N = 3–2, ${\text{}}J=\tfrac{5}{2}\mbox{--}\tfrac{5}{2}$, ${\text{}}F=\tfrac{7}{2}\mbox{--}\tfrac{7}{2}$ 33339.516640.73 ± 0.041.81.38 ± 0.1834.10.07
CN N = 3–2, ${\text{}}J=\tfrac{5}{2}\mbox{--}\tfrac{3}{2}$, ${\text{}}F=\tfrac{5}{2}\mbox{--}\tfrac{5}{2}$ 33340.008130.95 ± 0.042.12.16 ± 0.2033.90.07
CN N = 3–2, ${\text{}}J=\tfrac{5}{2}\mbox{--}\tfrac{3}{2}$, ${\text{}}F=\tfrac{3}{2}\mbox{--}\tfrac{3}{2}$ 33340.019630.93 ± 0.041.81.81 ± 0.1734.10.07
CN N = 3–2, ${\text{}}J=\tfrac{5}{2}\mbox{--}\tfrac{3}{2}$, ${\text{}}F=\tfrac{7}{2}\mbox{--}\tfrac{5}{2}$ 33340.031553.08 ± 0.042.78.71 ± 0.2533.80.07
CN N = 3–2, ${\text{}}J=\tfrac{5}{2}\mbox{--}\tfrac{3}{2}$, ${\text{}}F=\tfrac{5}{2}\mbox{--}\tfrac{3}{2}$ 33340.035413.04 ± 0.042.16.87 ± 0.2633.70.07(1)
CN N = 3–2, ${\text{}}J=\tfrac{7}{2}\mbox{--}\tfrac{5}{2}$, ${\text{}}F=\tfrac{9}{2}\mbox{--}\tfrac{7}{2}$ 33340.247774.38 ± 0.032.411.32 ± 0.2233.40.07(1)
CN N = 3–2, ${\text{}}J=\tfrac{7}{2}\mbox{--}\tfrac{5}{2}$, ${\text{}}F=\tfrac{5}{2}\mbox{--}\tfrac{5}{2}$ 33340.261770.91 ± 0.041.91.85 ± 0.1834.10.07
CN N = 3–2, ${\text{}}J=\tfrac{7}{2}\mbox{--}\tfrac{5}{2}$, ${\text{}}F=\tfrac{7}{2}\mbox{--}\tfrac{7}{2}$ 33340.264951.02 ± 0.042.02.12 ± 0.1833.90.07
NO ${\text{}}J=\tfrac{7}{2}\mbox{--}\tfrac{5}{2}$, ${\rm{\Omega }}=\tfrac{1}{2}$, ${\text{}}F=\tfrac{9}{2}$ +$\tfrac{7}{2}$ 36351.043520.29 ± 0.032.50.78 ± 0.2233.70.08
NO ${\text{}}J=\tfrac{7}{2}\mbox{--}\tfrac{5}{2}$, ${\rm{\Omega }}=\tfrac{1}{2}$, ${\text{}}F=\tfrac{7}{2}$ +$\tfrac{5}{2}$ 36351.051710.50 ± 0.042.11.10 ± 0.2034.30.08(2)
HNCO114, 7–104, 6 720241.498640.32 ± 0.084.81.20 ± 0.1333.80.04(2)
HNCO113, 9–103, 8 445241.619300.51 ± 0.024.12.19 ± 0.2533.60.04(2)
HNCO112, 10–102, 9 240241.70385<0.60<2.60.04(3)
HNCO110, 11–100, 10 70241.774030.93 ± 0.024.94.87 ± 0.2634.60.04
HNCO111, 10–101, 9 113242.639700.79 ± 0.025.04.18 ± 0.2734.70.04
HNCO161, 16–151, 15 186350.333060.69 ± 0.045.13.73 ± 0.4434.50.08
HNCO164, 13–154, 12 794351.24085<0.25<1.10.08(3)
HNCO163, 14–153, 13 518351.416800.33 ± 0.045.21.83 ± 0.4534.40.08(2)
HNCO162, 15–152, 14 314351.537800.43 ± 0.035.42.47 ± 0.4934.10.08
HNCO162, 14–152, 13 314351.551570.46 ± 0.035.82.82 ± 0.5335.20.08
HNCO160, 16–150, 15 143351.633260.72 ± 0.044.03.02 ± 0.4134.60.08
HNCO231, 23–240, 24 333351.994870.33 ± 0.035.51.91 ± 0.4735.90.08
CH3CN1410–1310 806257.033440.14 ± 0.022.40.36 ± 0.1034.00.03(2)
CH3CN149–13−9 671257.12704<0.35<1.50.03(2) (4)
CH3CN148–138 549257.210880.24 ± 0.016.31.64 ± 0.2734.90.03(2)
CH3CN147–137 442257.284940.42 ± 0.024.92.20 ± 0.2134.30.03(2)
CH3CN146–13−6 350257.349180.90 ± 0.024.74.51 ± 0.2034.40.03(2)
CH3CN145–135 271257.40358<1.00<4.30.03(2) (3)
CH3CN144–134 207257.448131.14 ± 0.024.35.22 ± 0.1934.40.03(2)
CH3CN143–13−3 157257.482791.55 ± 0.024.67.55 ± 0.2034.50.03(2)
CH3CN142–132 121257.507561.56 ± 0.024.47.34 ± 0.2034.60.03(2)
CH3CN141–131 100257.522431.63 ± 0.023.86.61 ± 0.1834.70.03(2)
CH3CN140–130 93257.527381.69 ± 0.024.37.79 ± 0.1834.40.03
CH3CN196–18−6 425349.212310.73 ± 0.043.93.07 ± 0.3534.20.08(2)
CH3CN195–185 346349.286010.81 ± 0.043.42.97 ± 0.3034.30.08(2)
CH3CN194–184 282349.346340.92 ± 0.034.34.18 ± 0.4034.40.08(2)
CH3CN193–18−3 232349.393301.24 ± 0.034.15.38 ± 0.3934.40.08(5)
CH3CN192–182 196349.426851.04 ± 0.044.24.72 ± 0.3734.60.08(2)
CH3CN191–181 175349.446991.25 ± 0.034.15.42 ± 0.3834.50.08(5)
CH3CN190–180 168349.453701.23 ± 0.043.95.10 ± 0.3834.20.08
13CH3CN190–180 163339.36630<0.11<0.450.05
HC3N27–26165245.606321.55 ± 0.034.27.02 ± 0.2534.30.04

Note. (1) Blend of three hyperfine components. (2) Blend of three two components. (3) Blend with CH3OH. (4) Blend with HCOOCH3. (5) Blend of four hyperfine components.

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Table A3. Line Parameters for Si- and S-bearing Molecules

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
SiO6–544260.518010.64 ± 0.022.71.86 ± 0.1334.10.03
SO NJ = 66–55 56258.255835.34 ± 0.023.620.20 ± 0.1934.10.03
SO NJ = 33–23 26339.341460.49 ± 0.043.41.76 ± 0.3434.00.07
SO NJ = 87–76 81340.714163.85 ± 0.043.915.81 ± 0.3934.20.07
34SO NJ = 33–23 25337.89225<0.15<0.60.07
34SO NJ = 89–78 77339.857270.69 ± 0.044.43.26 ± 0.3833.00.07
33SO NJ = 67–56 47259.284030.34 ± 0.076.80.81 ± 0.0633.50.03(1) (2)
CS5–435244.9355614.57 ± 0.033.249.51 ± 0.2033.90.04
C33S5–435242.913611.31 ± 0.023.75.18 ± 0.2134.20.04
C33S7–665340.052571.05 ± 0.043.94.35 ± 0.3434.30.07
C34S7–665337.396462.46 ± 0.043.38.65 ± 0.3134.10.07
H2CS71, 6–61, 5 60244.048502.91 ± 0.033.09.37 ± 0.1934.20.04
H2CS101, 10–91, 9 102338.083191.68 ± 0.043.97.04 ± 0.3634.20.07
OCS20–19123243.218041.82 ± 0.034.28.17 ± 0.2434.30.04
OCS28–27237340.449271.26 ± 0.044.05.40 ± 0.3934.50.07
OCS29–28254352.599571.05 ± 0.044.55.01 ± 0.4034.30.08
O13CS20–19122242.435430.20 ± 0.024.81.00 ± 0.3234.90.04
SO2 52, 4–41, 3 24241.615800.88 ± 0.025.14.79 ± 0.2834.20.04(3)
SO2 268, 18–277, 21 480243.24543<0.10<0.40.04
SO2 140, 14–131, 13 94244.254221.15 ± 0.026.37.67 ± 0.3334.20.04
SO2 263, 23–254, 22 351245.339230.41 ± 0.022.81.21 ± 0.1534.50.04
SO2 103, 7–102, 8 73245.563421.04 ± 0.025.35.86 ± 0.2734.30.04
SO2 73, 5–72, 6 48257.099970.96 ± 0.025.65.76 ± 0.2434.20.03(4)
SO2 324, 28–323, 29 531258.388720.46 ± 0.024.12.01 ± 0.2133.90.03
SO2 207, 13–216, 16 313258.666970.32 ± 0.073.40.76 ± 0.0833.10.03(2)
SO2 93, 7–92, 8 63258.942200.91 ± 0.025.45.26 ± 0.2334.40.03
SO2 184, 14–183, 15 197338.305990.65 ± 0.034.43.09 ± 0.3734.00.07
SO2 201, 19–192, 18 199338.61181<0.90<3.80.07(5)
SO2 282, 26–281, 27 392340.316410.48 ± 0.036.03.02 ± 0.5034.50.07
SO2 53, 3–42, 2 36351.257220.75 ± 0.045.94.73 ± 0.5134.10.08
SO2 144, 10–143, 11 136351.873870.70 ± 0.034.43.32 ± 0.3834.00.08
34SO2 140, 14–131, 13 94244.481520.34 ± 0.021.50.54 ± 0.0933.60.04
13CH3SH141, 14–131, 13 A131350.00956<0.15<0.70.08

Note. (1) Blend of four hyperfine components. (2) The integrated intensity is calculated by directly integrating the spectrum. (3) Partial blend with HNCO. (4) Blend with HCOOCH3. (5) Blend with CH3OH.

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Table A4. Line Parameters for CH3OH, 13CH3OH, and CH2DOH

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
CH3OH253 A–252 A+ 804241.588760.72 ± 0.024.53.49 ± 0.2534.50.04
CH3OH50 E–40 E48241.700162.45 ± 0.034.010.57 ± 0.2434.20.04
CH3OH5−1 E–4−1 E40241.767233.70 ± 0.033.212.53 ± 0.2034.20.04
CH3OH50 A+–40 A+ 35241.791354.15 ± 0.033.013.29 ± 0.1934.10.04
CH3OH54 A–44 A 115241.806521.46 ± 0.024.36.65 ± 0.2334.70.04(1)
CH3OH5−4 E–4−4 E123241.813251.33 ± 0.024.36.13 ± 0.2334.70.04
CH3OH53 A+–43 A+ 85241.832722.08 ± 0.024.29.35 ± 0.2534.30.04(2)
CH3OH52 A–42 A 73241.842282.13 ± 0.025.011.37 ± 0.2633.70.04(1)
CH3OH5−3 E–4−3 E98241.852301.54 ± 0.024.47.13 ± 0.2334.60.04
CH3OH51 E–41 E56241.879032.26 ± 0.033.99.26 ± 0.2334.40.04
CH3OH52 A+–42 A+ 73241.887671.82 ± 0.033.97.63 ± 0.2334.50.04
CH3OH5−2E–4−2 E61241.904152.94 ± 0.033.811.83 ± 0.2134.00.04(1)
CH3OH14−1 E–13−2 E249242.446081.28 ± 0.024.86.55 ± 0.2534.60.04(3)
CH3OH243 A–242 A+ 746242.490240.88 ± 0.024.64.30 ± 0.2534.40.04
CH3OH51 A–41 A 50243.915792.75 ± 0.023.610.69 ± 0.2134.30.04
CH3OH223 A–222 A+ 637244.330371.06 ± 0.024.95.54 ± 0.2734.60.04
CH3OH91 E–80 E, νt = 1396244.337981.08 ± 0.024.75.38 ± 0.2534.60.04
CH3OH18−6 E–17−7 E, νt = 1889245.094500.31 ± 0.024.11.35 ± 0.2634.30.04
CH3OH213 A–212 A+ 586245.223021.22 ± 0.034.25.50 ± 0.2434.40.04
CH3OH183 A+–182 A 447257.402091.50 ± 0.026.09.52 ± 0.2534.00.03(4)
CH3OH193 A+–192 A 491258.780251.22 ± 0.025.47.05 ± 0.2334.10.03
CH3OH172 A–161 A, νt = 1653259.273690.79 ± 0.024.23.54 ± 0.1934.60.03
CH3OH241 E–240 E717259.581400.62 ± 0.024.42.89 ± 0.1834.70.03
CH3OH20−8 E–21−7 E808260.064320.43 ± 0.023.81.75 ± 0.1734.80.03
CH3OH203 A+–202 A 537260.381461.22 ± 0.014.76.02 ± 0.2534.30.03
CH3OH74 A+–64A+, νt = 2679337.273560.59 ± 0.044.32.68 ± 0.4934.50.07(1)
CH3OH7−2 E–6−2 E, νt =2710337.279180.54 ± 0.032.71.54 ± 0.4834.80.07
CH3OH70 A+–60 A+, νt = 2573337.284320.78 ± 0.035.34.36 ± 0.4534.70.07
CH3OH71 A+–61 A+, νt = 1390337.297480.97 ± 0.034.14.25 ± 0.3935.30.07(1)
CH3OH72 E–62 E, νt = 2651337.302640.65 ± 0.034.22.94 ± 0.3934.50.07
CH3OH7−1 E–6−1 E, νt = 2597337.312360.57 ± 0.044.72.87 ± 0.4134.30.07
CH3OH76 A+–66 A+, νt = 1533337.463700.62 ± 0.045.53.62 ± 0.4734.60.07(1)
CH3OH100 E–9−9 E, νt = 1916337.472590.40 ± 0.045.62.38 ± 0.4733.80.07
CH3OH7−6 E–6−6 E, νt = 1558337.490560.71 ± 0.044.33.23 ± 0.3634.80.07(5)
CH3OH73 E–63 E, νt = 1482337.519140.80 ± 0.044.33.68 ± 0.3834.90.07
CH3OH75 A+–65 A+, νt = 1485337.546120.84 ± 0.044.74.19 ± 0.3934.70.07(1)
CH3OH74 E–64 E, νt = 1428337.58168<1.00<4.30.07(6)
CH3OH7−2 E–6−2 E, νt = 1429337.605290.87 ± 0.033.83.51 ± 0.5335.00.07
CH3OH7−3 E–6−3 E, νt = 1387337.610661.01 ± 0.033.74.03 ± 0.3234.60.07(1)
CH3OH72 A+–62 A+, νt = 1363337.625751.03 ± 0.043.43.71 ± 0.3034.70.07
CH3OH72 A–62 A, νt = 1364337.635751.00 ± 0.034.14.34 ± 0.3934.60.07
CH3OH70 E–60 E, νt = 1365337.643911.26 ± 0.037.910.58 ± 0.7034.30.07(2)
CH3OH73 A+–63 A+, νt = 1461337.655200.98 ± 0.033.23.34 ± 0.3334.40.07(1)
CH3OH74 A+–64 A+, νt = 1546337.685610.92 ± 0.044.03.89 ± 0.3734.90.07(2)
CH3OH7−1 E–6−1 E, νt = 1478337.707570.83 ± 0.044.94.39 ± 0.4434.50.07
CH3OH70 A+–60 A+, νt = 1488337.748830.88 ± 0.044.23.96 ± 0.3634.90.07
CH3OH20−6 E–21−5 E676337.837800.45 ± 0.043.51.69 ± 0.3034.60.07
CH3OH71 A–61 A, νt = 2748337.877550.51 ± 0.043.21.75 ± 0.2834.60.07
CH3OH71 A–61 A, νt = 1390337.969440.89 ± 0.044.44.13 ± 0.3834.50.07
CH3OH70 E–60 E78338.124492.19 ± 0.043.47.84 ± 0.3034.40.07
CH3OH7−1 E–6−1 E71338.344592.91 ± 0.043.510.81 ± 0.3234.20.07
CH3OH76 E–66 E244338.404610.98 ± 0.043.84.00 ± 0.3334.70.07
CH3OH70 A+–60 A+ 65338.408703.41 ± 0.032.910.59 ± 0.2834.10.07
CH3OH7−6 E–6−6 E254338.430970.88 ± 0.034.64.25 ± 0.3834.60.07
CH3OH76 A+–66 A+ 259338.442371.04 ± 0.044.34.79 ± 0.3634.70.07(1)
CH3OH7−5 E–6−5 E189338.456541.12 ± 0.034.75.62 ± 0.3934.50.07
CH3OH75 E–65 E201338.475231.15 ± 0.034.15.02 ± 0.3434.60.07
CH3OH75 A+–65 A+ 203338.486321.22 ± 0.034.96.42 ± 0.4234.50.07(1)
CH3OH7−4 E–6−4 E153338.504071.31 ± 0.034.76.52 ± 0.4134.80.07
CH3OH74 E–64 E161338.530261.30 ± 0.044.25.87 ± 0.3534.40.07
CH3OH73 A+–63 A+ 115338.540831.95 ± 0.045.511.45 ± 0.4733.30.07(1)
CH3OH7−3 E–6−3 E128338.559961.40 ± 0.044.56.74 ± 0.3834.40.07
CH3OH73 E–63 E113338.583221.46 ± 0.044.36.70 ± 0.3734.60.07
CH3OH71 E–61 E86338.614941.95 ± 0.044.49.18 ± 0.3834.40.07
CH3OH72 A+–62 A+ 103338.639801.60 ± 0.044.16.97 ± 0.3434.50.07
CH3OH7−2 E–6−2 E91338.722902.52 ± 0.044.110.98 ± 0.3534.90.07(1)
CH3OH213 E–212 E, νt = 1951339.42217<0.18<0.80.07
CH3OH22 A+–31 A+ 45340.141141.08 ± 0.034.45.05 ± 0.3835.20.07
CH3OH166 A–175 A 509340.393660.90 ± 0.044.03.87 ± 0.3434.70.07
CH3OH111 E–100 E, νt = 1444340.683970.98 ± 0.035.15.29 ± 0.4634.80.07
CH3OH153 E–164 E, νt = 1695350.286490.70 ± 0.034.93.65 ± 0.4234.60.08
CH3OH40 E–3−1 E36350.687661.87 ± 0.044.69.18 ± 0.4034.10.08
CH3OH183 E–182 E, νt = 1812350.72388<0.25<1.10.08
CH3OH11 A+–00 A+ 17350.905102.38 ± 0.043.79.29 ± 0.3334.40.08
CH3OH95 E–104 E241351.236480.97 ± 0.044.74.82 ± 0.4034.50.08
13CH3OH42 A–51 A 60242.373150.17 ± 0.025.10.93 ± 0.2736.30.04
13CH3OH153 A+–152 A 322257.421790.48 ± 0.023.92.02 ± 0.1834.50.03
13CH3OH163 A+–162 A 358258.153000.59 ± 0.024.62.90 ± 0.1934.80.03(7)
13CH3OH173 A+–172 A 396259.03649<0.20<0.90.03(8)
13CH3OH21 E–10 E28259.986530.54 ± 0.022.91.68 ± 0.1634.50.03(9)
13CH3OH130 A+–121 A+ 206338.759950.60 ± 0.043.72.33 ± 0.3234.40.07
13CH3OH11 A+–00 A+ 17350.103120.58 ± 0.043.11.87 ± 0.2834.70.08
13CH3OH81 E–72 E103350.421580.49 ± 0.044.62.38 ± 0.4134.00.08
CH2DOH112, 9 o1–111, 10 o1 177242.033600.32 ± 0.031.80.60 ± 0.1433.20.04
CH2DOH52, 3 e0–51, 4 e0 48243.225990.56 ± 0.022.91.74 ± 0.1735.50.04
CH2DOH42, 2 e0–41, 3 e0 38244.841130.35 ± 0.024.21.55 ± 0.2534.40.04
CH2DOH102, 8 o1–101, 9 o1 153244.988850.13 ± 0.023.90.54 ± 0.2234.70.04
CH2DOH52, 3 o1–51, 4 o1 68257.394510.26 ± 0.022.20.61 ± 0.1034.40.03
CH2DOH42, 3 e1–31, 3 o1 48257.895670.30 ± 0.022.30.72 ± 0.0934.60.03
CH2DOH42, 3 e0–41, 4 e0 38258.337110.42 ± 0.022.81.25 ± 0.1234.30.03
CH2DOH90, 9 e0–81, 8 e0 96337.348660.63 ± 0.042.81.84 ± 0.2535.10.07
CH2DOH61, 6 e0–50, 5 e0 48338.957110.39 ± 0.043.51.46 ± 0.3235.10.07
CH2DOH152, 14 o1–151, 14 e1 292339.485720.24 ± 0.032.20.56 ± 0.2034.90.07
CH2DOH62, 4 e1–51, 4 o1 72340.127090.42 ± 0.033.51.55 ± 0.4334.80.07
CH2DOH131,13 e0–120, 12 e1 196340.243440.57 ± 0.032.91.76 ± 0.3334.20.07(10)
CH2DOH22, 1 e0–11, 0 e0 23340.348290.29 ± 0.043.71.15 ± 0.3234.10.07
CH2DOH134, 9 e1–133, 11 o1 267349.183830.24 ± 0.042.20.57 ± 0.2234.30.08
CH2DOH124, 8 e1–123, 10 o1 239349.356130.22 ± 0.043.10.75 ± 0.3035.30.08
CH2DOH114, 8 e1–113, 8 o1 213349.495210.22 ± 0.043.70.85 ± 0.3234.30.08(11)
CH2DOH114, 7 e1–113, 9 o1 213349.508870.47 ± 0.041.60.80 ± 0.2234.80.08
CH2DOH104, 6 e1–103, 8 o1 190349.643600.32 ± 0.042.80.97 ± 0.2834.40.08
CH2DOH94, 5 e1–93, 7 o1 168349.761680.30 ± 0.047.22.31 ± 0.6236.40.08(12)
CH2DOH84, 5 e1–83, 5 o1 149349.862110.34 ± 0.046.02.15 ± 0.5533.40.08(12)
CH2DOH74, 4 e1–73, 4 o1 132349.951680.48 ± 0.033.41.73 ± 0.2934.30.08(12)
CH2DOH64, 3 e1–63, 3 o1 117350.027350.64 ± 0.042.41.60 ± 0.2634.20.08(12)
CH2DOH54, 2 e1–53, 2 o1 104350.090240.57 ± 0.042.01.21 ± 0.2334.20.08(12)
CH2DOH44, 1 e1–43, 1 o1 94350.141300.33 ± 0.034.01.41 ± 0.3733.80.08(12)
CH2DOH62, 5 e1–51, 5 o1 72350.453870.53 ± 0.032.61.46 ± 0.2834.20.08
CH2DOH51, 4 e1–50, 5 e0 49350.632070.58 ± 0.043.21.98 ± 0.3235.20.08
CH2DOH22, 1 o1–11, 0 o1 42351.60685<0.15<0.70.08
CH2DOH81, 8 e0–71, 7 e0 80351.796430.54 ± 0.042.51.44 ± 0.3034.40.08
CH2DOH22, 0 o1–11, 1 o1 42352.34437<0.15<0.70.08
CH2DOH81, 8 e1–71, 7 e1 93352.801960.40 ± 0.042.61.10 ± 0.2334.40.08

Note. (1) Blend of two CH3OH lines with similar spectroscopic constants. (2) Blend of three CH3OH lines with similar spectroscopic constants. (3) Possible blend with C2H5OH. (4) Blend with CH3CN. (5) Blend with HCOOCH3. (6) Blend with 34SO. (7) Partial blend with HC15N. (8) Possible blend with HDCO. (9) Blend with CH3OCH3. (10) Partial blend with CN. (11) Tentative detection. (12) Blend of two CH2DOH lines with similar spectroscopic constants.

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Table A5. Line Parameters for C2H5OH

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
C2H5OH1411, 3–1311, 2 297242.175480.15 ± 0.025.40.87 ± 0.4034.70.04(1)
C2H5OH149, 5–139, 4 248242.221290.16 ± 0.025.50.93 ± 0.2933.70.04(1)
C2H5OH148, 6–138, 5 228242.271150.13 ± 0.024.10.57 ± 0.2334.60.04(1)
C2H5OH147, 8–137, 7 209242.349840.30 ± 0.024.11.30 ± 0.2335.70.04(1)
C2H5OH1410, 4–1310, 3 266242.429870.36 ± 0.021.60.62 ± 0.0835.30.04(2)
C2H5OH146, 9–136, 8 193242.475500.35 ± 0.024.31.60 ± 0.2334.60.04(1)
C2H5OH147, 8–137, 7 204242.524220.37 ± 0.021.50.57 ± 0.0834.90.04(1)
C2H5OH146, 9–136, 8 188242.625610.42 ± 0.021.50.67 ± 0.0834.60.04(1)
C2H5OH145, 10–135, 9 180242.685020.13 ± 0.023.60.51 ± 0.1934.60.04(1)
C2H5OH145, 9–135, 8 180242.693050.35 ± 0.021.50.56 ± 0.0834.70.04
C2H5OH143, 12–133, 11 160242.770110.15 ± 0.023.40.55 ± 0.1735.20.04
C2H5OH145, 10–135, 9 175242.816440.09 ± 0.023.30.33 ± 0.1833.80.04(3)
C2H5OH145, 9–135, 8 175242.825120.10 ± 0.023.90.42 ± 0.2135.60.04
C2H5OH144, 11–134, 10 169242.995970.28 ± 0.033.10.91 ± 0.1934.20.04
C2H5OH144, 11–134, 10 164243.120340.38 ± 0.021.50.58 ± 0.0835.20.04
C2H5OH144, 10–134, 9 169243.206530.36 ± 0.021.70.64 ± 0.0934.30.04
C2H5OH141, 13–131, 12 152244.633960.24 ± 0.023.80.99 ± 0.2134.50.04
C2H5OH143, 11–133, 10 160245.327150.39 ± 0.021.40.60 ± 0.0834.60.04
C2H5OH161, 15–152, 14 117257.060900.26 ± 0.025.31.49 ± 0.2334.10.03
C2H5OH143, 11–132, 11 156259.322640.09 ± 0.024.30.40 ± 0.1934.20.03(3)
C2H5OH159, 6–149, 5 261259.539130.28 ± 0.022.40.71 ± 0.1034.40.03(1)
C2H5OH157, 9–147, 8 222259.697900.11 ± 0.024.70.57 ± 0.2134.40.03(1)
C2H5OH1510, 5–1410, 4 279259.756530.27 ± 0.022.40.69 ± 0.1434.90.03(1)
C2H5OH159, 6–149, 5 255259.777140.28 ± 0.021.50.43 ± 0.0734.50.03(1)
C2H5OH158, 8–148, 7 235259.814440.29 ± 0.022.30.72 ± 0.1034.00.03(1)
C2H5OH156, 10–146, 9 206259.852180.30 ± 0.022.30.74 ± 0.1034.70.03(1)
C2H5OH157, 9–147, 8 216259.885070.28 ± 0.023.10.93 ± 0.1334.70.03(1)
C2H5OH153, 13–143, 12 172260.046640.28 ± 0.022.20.64 ± 0.1035.20.03
C2H5OH155, 11–145, 10 192260.107610.09 ± 0.014.70.43 ± 0.2434.50.03(3)
C2H5OH155, 10–145, 9 192260.122760.11 ± 0.024.60.52 ± 0.2034.50.03
C2H5OH153, 13–143, 12 168260.141680.29 ± 0.023.51.06 ± 0.1534.90.03
C2H5OH155, 10–145, 9 187260.266130.27 ± 0.022.50.71 ± 0.1133.90.03
C2H5OH154, 12–144, 11 181260.457730.12 ± 0.024.40.57 ± 0.1935.10.03
C2H5OH154, 12–144, 11 176260.591330.28 ± 0.022.40.74 ± 0.1034.50.03
C2H5OH202, 19–192, 18 234338.887920.39 ± 0.045.02.07 ± 0.4335.50.07(4)
C2H5OH167, 9–166, 10 176338.671730.35 ± 0.044.71.76 ± 0.4033.40.07(1)
C2H5OH147, 7–146, 8 150339.061060.28 ± 0.034.01.21 ± 0.3434.50.07(1)
C2H5OH137, 6–136, 7 138339.201540.38 ± 0.031.90.79 ± 0.2533.90.07(1)
C2H5OH127, 5–126, 6 127339.312530.24 ± 0.034.91.24 ± 0.4035.90.07
C2H5OH117, 4–116, 5 117339.398440.25 ± 0.034.01.07 ± 0.3334.60.07(1)
C2H5OH87, 1–86, 2 92339.544090.30 ± 0.042.10.67 ± 0.2034.40.07(1)
C2H5OH94, 6–83, 5 58339.978920.24 ± 0.043.80.97 ± 0.3235.00.07
C2H5OH204, 16–194, 15 252350.365060.40 ± 0.043.91.65 ± 0.3335.70.08(5)
C2H5OH202, 19–191, 18 179350.534350.30 ± 0.043.31.06 ± 0.2934.90.08
C2H5OH135, 8–124, 8 163351.965480.25 ± 0.032.00.55 ± 0.1835.30.08

Note. (1) Blend of two C2H5OH lines with similar spectroscopic constants. (2) Blend of four C2H5OH lines with similar spectroscopic constants. (3) Tentative detection. (4) Blend of three C2H5OH lines with similar spectroscopic constants. (5) Possible blend with CH3CHO.

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Table A6. Line Parameters for HCOOCH3

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
HCOOCH3 204, 17–194, 16 A νt = 1322242.610070.35 ± 0.022.40.92 ± 0.1434.30.04
HCOOCH3 195, 14–185, 13 A130242.896030.74 ± 0.023.62.85 ± 0.1934.50.04
HCOOCH3 194, 15–184, 14 A νt = 1313244.066670.35 ± 0.023.41.28 ± 0.1834.40.04
HCOOCH3 2010, 10–1910, 9 E νt = 1378244.112420.13 ± 0.024.00.56 ± 0.2233.90.04
HCOOCH3 2012, 8–1912, 7 A νt = 1407244.198300.17 ± 0.024.80.89 ± 0.2534.50.04(1)
HCOOCH3 2010, 11–1910, 10 A νt = 1377244.528540.38 ± 0.023.01.21 ± 0.1634.70.04(1)
HCOOCH3 204, 17–194, 16 E135244.580340.74 ± 0.024.63.64 ± 0.2434.70.04
HCOOCH3 204, 17–194, 16 A135244.594050.78 ± 0.023.63.02 ± 0.1934.80.04
HCOOCH3 2011, 10–1911, 9 E νt = 1391244.729660.29 ± 0.032.20.67 ± 0.1234.10.04
HCOOCH3 209, 12–199, 11 A νt = 1365244.845340.43 ± 0.022.91.33 ± 0.1734.30.04(1)
HCOOCH3 194, 15–184, 14 E νt = 1313244.902130.30 ± 0.023.61.17 ± 0.1934.40.04
HCOOCH3 2010, 11–1910, 10 E νt = 1377245.082710.15 ± 0.024.00.65 ± 0.2235.30.04
HCOOCH3 208, 12–198, 11 E νt = 1354245.261740.17 ± 0.025.00.88 ± 0.2634.70.04
HCOOCH3 208, 13–198, 12 A νt = 1354245.342550.34 ± 0.023.21.14 ± 0.1934.20.04
HCOOCH3 209, 12–199, 11 E νt = 1365245.543880.28 ± 0.022.50.75 ± 0.1335.00.04
HCOOCH3 2015, 5–1915, 4 A273245.651210.42 ± 0.023.21.43 ± 0.1734.70.04(1)
HCOOCH3 2015, 5–1915, 4 E273245.656780.29 ± 0.023.10.98 ± 0.1734.50.04
HCOOCH3 2015, 6–1915, 5 E273245.672980.33 ± 0.022.40.83 ± 0.1334.10.04
HCOOCH3 232, 22–222, 21 A νt = 1343256.999360.36 ± 0.024.21.62 ± 0.1834.80.03
HCOOCH3 231, 22–221, 21 A νt = 1343257.015470.36 ± 0.023.61.39 ± 0.1634.30.03
HCOOCH3 219, 12–209, 11 E νt = 1377257.049780.46 ± 0.024.52.18 ± 0.1934.20.03
HCOOCH3 205, 15–195, 14 E143257.226610.69 ± 0.024.13.03 ± 0.1734.60.03
HCOOCH3 205, 15–195, 14 A143257.252670.76 ± 0.024.43.58 ± 0.2134.40.03(1)
HCOOCH3 219, 13–209, 12 A νt = 1377257.297790.42 ± 0.023.71.66 ± 0.1634.00.03(1)
HCOOCH3 204, 16–194, 15 E νt = 1325257.588890.38 ± 0.024.61.86 ± 0.2135.40.03
HCOOCH3 223, 20–213, 19 E152257.690330.72 ± 0.023.72.88 ± 0.1634.60.03
HCOOCH3 223, 20–213, 19 A152257.699490.73 ± 0.023.52.75 ± 0.1534.50.03
HCOOCH3 218, 13–208, 12 E νt = 1366257.831090.27 ± 0.023.71.05 ± 0.1634.10.03
HCOOCH3 218, 14–208, 13 A νt = 1366257.889870.24 ± 0.022.30.59 ± 0.1133.80.03
HCOOCH3 218, 13–208, 12 A νt = 1366257.906130.26 ± 0.022.40.66 ± 0.1135.30.03
HCOOCH3 2116, 5–2016, 4 E306257.919890.25 ± 0.023.50.93 ± 0.1534.00.03
HCOOCH3 2116, 6–2016, 5 E306257.933830.21 ± 0.023.20.73 ± 0.1534.70.03
HCOOCH3 2115, 6–2015, 5 A285258.001760.46 ± 0.023.21.55 ± 0.1434.40.03(1)
HCOOCH3 241, 24–231, 23 A νt = 1345258.010750.63 ± 0.013.92.58 ± 0.1834.50.03(2)
HCOOCH3 2115, 7–2015, 6 E285258.024240.30 ± 0.022.20.69 ± 0.1135.00.03
HCOOCH3 219, 13–209, 12 E νt = 1377258.037970.31 ± 0.021.40.48 ± 0.0633.70.03
HCOOCH3 241, 24–231, 23 E νt = 1345258.055040.69 ± 0.024.93.57 ± 0.2135.00.03(1)
HCOOCH3 222, 20–212, 19 E152258.081040.85 ± 0.025.44.93 ± 0.2334.30.03
HCOOCH3 222, 20–212, 19 A152258.089490.76 ± 0.023.93.14 ± 0.1834.60.03
HCOOCH3 2114, 7–2014, 6 A266258.121190.69 ± 0.024.53.26 ± 0.2033.90.03(2)
HCOOCH3 2114, 8–2014, 7 E266258.142090.35 ± 0.023.81.41 ± 0.1634.70.03
HCOOCH3 2113, 8–2013, 7 A248258.277430.84 ± 0.016.35.64 ± 0.3636.00.03(2)
HCOOCH3 2112, 9–2012, 8 E232258.476450.47 ± 0.015.12.58 ± 0.2435.30.03
HCOOCH3 2112, 9–2012, 8 A232258.482980.62 ± 0.025.83.84 ± 0.2734.90.03(1)
HCOOCH3 232, 22–222, 21 E156258.490870.79 ± 0.023.93.27 ± 0.1734.70.03
HCOOCH3 232, 22–222, 21 A156258.496240.83 ± 0.015.04.38 ± 0.2834.40.03(1)
HCOOCH3 231, 22–221, 21 E156258.502730.81 ± 0.013.53.00 ± 0.1834.60.03
HCOOCH3 231, 22–221, 21 A156258.508180.85 ± 0.023.32.97 ± 0.1434.50.03
HCOOCH3 215, 17–205, 16 A νt = 1341258.701050.33 ± 0.022.70.93 ± 0.1234.30.03
HCOOCH3 2111, 10–2011, 9 E217258.746250.50 ± 0.023.51.84 ± 0.1535.00.03
HCOOCH3 2111, 11–2011, 10 A217258.756670.62 ± 0.024.93.20 ± 0.2134.90.03(1)
HCOOCH3 2111, 11–2011, 10 E217258.769970.59 ± 0.024.83.03 ± 0.2035.10.03(1)
HCOOCH3 213, 18–203, 17 A νt = 1333258.775320.35 ± 0.022.91.07 ± 0.1235.10.03
HCOOCH3 217, 14–207, 13 A νt = 1356259.003870.39 ± 0.024.31.77 ± 0.3234.20.03
HCOOCH3 217, 14–207, 13 E νt = 1356259.025830.29 ± 0.022.20.67 ± 0.0934.60.03
HCOOCH3 2110, 11–2010, 10 E203259.113950.46 ± 0.024.32.09 ± 0.1934.60.03
HCOOCH3 2110, 12–2010, 11 A203259.128180.77 ± 0.024.13.37 ± 0.1734.70.03(1)
HCOOCH3 2110, 12–2010, 11 E203259.137930.45 ± 0.023.41.63 ± 0.1434.60.03
HCOOCH3 213, 18–203, 17 E νt = 1333259.264990.28 ± 0.023.30.99 ± 0.1434.20.03
HCOOCH3 204, 16–194, 15 A139259.521810.68 ± 0.024.12.98 ± 0.1735.00.03
HCOOCH3 219, 12–209, 11 E190259.629300.46 ± 0.023.61.76 ± 0.1634.70.03
HCOOCH3 219, 13–209, 12 A190259.646530.85 ± 0.024.84.37 ± 0.2133.80.03(1)
HCOOCH3 219, 13–209, 12 E190259.653080.53 ± 0.023.52.01 ± 0.1534.40.03
HCOOCH3 213, 18–203, 17 E147260.244500.66 ± 0.024.12.89 ± 0.1734.70.03
HCOOCH3 218, 14–208, 13 A179260.392730.59 ± 0.023.52.22 ± 0.1534.60.03
HCOOCH3 218, 13–208, 12 A179260.415330.57 ± 0.024.02.42 ± 0.1734.60.03
HCOOCH3 278, 20–268, 19 A267337.503520.39 ± 0.042.91.19 ± 0.2934.80.07
HCOOCH3 278, 19–268, 18 A267338.355790.37 ± 0.043.41.33 ± 0.3134.70.07
HCOOCH3 277, 21–267, 20 E258338.396320.53 ± 0.034.42.46 ± 0.3934.90.07(1)
HCOOCH3 137, 7–126, 6 A86339.185910.19 ± 0.041.50.30 ± 0.1434.30.07(3)
HCOOCH3 137, 6–126, 7 A86339.196340.21 ± 0.032.70.63 ± 0.2534.70.07(3)
HCOOCH3 293, 26–283, 25 A νt = 1450339.882220.24 ± 0.043.80.99 ± 0.3434.60.07
HCOOCH3 285, 24–275, 23 E257340.741990.58 ± 0.044.93.03 ± 0.4234.30.07
HCOOCH3 285, 24–275, 23 A257340.754760.41 ± 0.035.32.33 ± 0.4534.70.07
HCOOCH3 295, 25–285, 24 E νt = 1460349.685480.26 ± 0.042.10.58 ± 0.2135.10.08
HCOOCH3 304, 27–294, 26 A νt = 1467350.132570.71 ± 0.032.01.48 ± 0.3033.50.08
HCOOCH3 303, 27–293, 26 A νt = 1467350.302540.33 ± 0.044.21.48 ± 0.3934.00.08
HCOOCH3 304, 27–294, 26 E νt = 1467350.550200.33 ± 0.043.71.27 ± 0.3733.90.08
HCOOCH3 276, 21–266, 20 E252350.919520.49 ± 0.034.42.27 ± 0.5234.60.08
HCOOCH3 276, 21–266, 20 A252350.947330.53 ± 0.043.92.21 ± 0.3534.40.08
HCOOCH3 287, 22–277, 21 E275350.998040.50 ± 0.044.32.29 ± 0.3734.80.08
HCOOCH3 287, 22–277, 21 A275351.015910.49 ± 0.044.92.57 ± 0.4335.20.08
HCOOCH3 295, 25–285, 24 E274351.517100.40 ± 0.044.71.99 ± 0.4035.20.08
HCOOCH3 295, 25–285, 24 A274351.529160.41 ± 0.044.62.02 ± 0.3935.00.08
HCOOCH3 288, 20–278, 19 E284351.823450.39 ± 0.044.01.67 ± 0.3534.60.08
HCOOCH3 288, 20–278, 19 A284351.842190.44 ± 0.043.41.59 ± 0.3035.00.08
HCOOCH3 304, 27–294, 26 E281352.282760.41 ± 0.043.01.31 ± 0.2834.60.08
HCOOCH3 304, 27–294, 26 A281352.292580.40 ± 0.044.51.87 ± 0.3834.70.08
HCOOCH3 303, 27–293, 26 E281352.404680.51 ± 0.042.01.09 ± 0.1734.10.08
HCOOCH3 303, 27–293, 26 A281352.414140.53 ± 0.043.72.09 ± 0.3234.40.08
HCOOCH3 331, 33–321, 32 A νt = 1479352.816840.32 ± 0.043.01.00 ± 0.2633.70.08(1)

Note. (1) Blend of two HCOOCH3 lines with similar spectroscopic constants. (2) Blend of three HCOOCH3 lines with similar spectroscopic constants. (3) Tentative detection.

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Table A7. Line Parameters for CH3OCH3

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
CH3OCH3 53, 2–42, 3 EE26241.528720.59 ± 0.025.03.12 ± 0.2633.30.04(1)
CH3OCH3 53, 2–42, 3 AA26241.531030.58 ± 0.025.23.23 ± 0.3236.30.04
CH3OCH3 213, 18–204, 17 EE226241.637300.25 ± 0.024.71.25 ± 0.2934.80.04(1)
CH3OCH3 131, 13–120, 12 EE81241.946540.92 ± 0.024.24.12 ± 0.2334.50.04(2)
CH3OCH3 232, 22–231, 23 EE253244.508300.16 ± 0.024.20.72 ± 0.2433.50.04
CH3OCH3 232, 22–231, 23 AA253244.512740.12 ± 0.023.30.40 ± 0.1734.50.04
CH3OCH3 182, 16–173, 15 EE164257.049880.46 ± 0.024.42.16 ± 0.1934.40.03(2)
CH3OCH3 273, 25–272, 26 EE356257.614530.09 ± 0.028.10.79 ± 0.3734.00.03(2) (3)
CH3OCH3 141, 14–130, 13 EE93258.549061.17 ± 0.024.45.43 ± 0.1934.20.03(2)
CH3OCH3 175, 12–174, 13 EE175259.311950.46 ± 0.079.03.34 ± 0.1635.00.03(2)
CH3OCH3 63, 4–52, 3 EE32259.489730.47 ± 0.013.01.48 ± 0.2034.40.03(1)
CH3OCH3 63, 4–52, 3 AA32259.493750.39 ± 0.012.91.21 ± 0.1934.40.03
CH3OCH3 235, 19–234, 20 EE287259.690070.41 ± 0.024.31.87 ± 0.1834.10.03(2)
CH3OCH3 215, 17–214, 18 EE246259.732150.47 ± 0.025.82.87 ± 0.2534.40.03(2)
CH3OCH3 205, 16–204, 17 EE227259.984410.53 ± 0.013.51.99 ± 0.2035.60.03(2)
CH3OCH3 245, 20–244, 21 EE309260.004390.43 ± 0.025.02.33 ± 0.2134.00.03(2)
CH3OCH3 195, 15–194, 16 EE208260.329220.46 ± 0.024.12.03 ± 0.2134.40.03(2)
CH3OCH3 255, 21–254, 22 EE332260.616850.35 ± 0.023.01.13 ± 0.1535.00.03(2)
CH3OCH3 212, 19–203, 18 AA220337.420460.57 ± 0.043.21.95 ± 0.3234.60.07
CH3OCH3 74, 4–63, 3 AE48337.723000.55 ± 0.042.31.33 ± 0.2835.10.07
CH3OCH3 74, 3–63, 3 EE48337.732190.40 ± 0.044.51.88 ± 0.3835.40.07
CH3OCH3 74, 4–63, 4 EE48337.778020.40 ± 0.033.81.59 ± 0.3233.80.07
CH3OCH3 74, 3–63, 4 AA48337.787210.71 ± 0.035.84.41 ± 0.5134.80.07
CH3OCH3 191, 18–182, 17 EE176339.491530.60 ± 0.043.92.50 ± 0.3334.50.07
CH3OCH3 103, 7–92, 8 EE63340.612620.45 ± 0.037.03.35 ± 0.5935.10.07
CH3OCH3 112, 9–101, 10 EE66349.806180.31 ± 0.044.61.52 ± 0.4133.60.08

Note. (1) Blend of three CH3OCH3 lines with similar spectroscopic constants. (2) Blend of four CH3OCH3 lines with similar spectroscopic constants. (3) Tentative detection.

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Table A8. Line Parameters for C2H5CN and NH2CHO

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
C2H5CN273, 25–263, 24 173241.625870.13 ± 0.024.90.69 ± 0.2933.30.04
C2H5CN279, 18–269, 17 253241.932180.23 ± 0.033.60.86 ± 0.2133.90.04(1)
C2H5CN2712, 15–2612, 14 322241.959050.12 ± 0.023.10.40 ± 0.1634.20.04(2)
C2H5CN278, 20–268, 19 234241.970450.30 ± 0.021.80.56 ± 0.1033.50.04(2)
C2H5CN2713, 14–2613, 13 350241.997100.12 ± 0.023.20.40 ± 0.1733.20.04(2)
C2H5CN277, 21–267, 20 217242.052490.23 ± 0.024.00.97 ± 0.2234.20.04(2)
C2H5CN276, 22–266, 21 203242.206980.30 ± 0.026.32.03 ± 0.3431.70.04(2)
C2H5CN274, 24–264, 23 181242.664690.32 ± 0.032.40.83 ± 0.1733.90.04
C2H5CN143, 11–132, 12 55245.023650.32 ± 0.022.30.77 ± 0.1435.10.04
C2H5CN300, 30–290, 29 194257.310640.11 ± 0.023.70.43 ± 0.1634.20.03
C2H5CN301, 30–290, 29 194257.583610.20 ± 0.021.50.32 ± 0.0633.60.03
C2H5CN299, 21–289, 20 277259.862760.11 ± 0.023.50.42 ± 0.1533.90.03(2)
C2H5CN2912, 17–2812, 16 347259.869890.35 ± 0.021.40.53 ± 0.0833.40.03(2)
C2H5CN2913, 16–2813, 15 374259.906640.09 ± 0.023.20.31 ± 0.1433.50.03(2) (3)
C2H5CN296, 24–286, 23 227260.221660.24 ± 0.023.10.80 ± 0.1534.80.03
C2H5CN295, 25–285, 24 215260.535690.27 ± 0.023.71.04 ± 0.1634.30.03
NH2CHO130, 13–121, 12 91244.85421<0.08<0.30.04
NH2CHO132, 12–131, 13 104258.636380.10 ± 0.023.90.40 ± 0.1735.60.03(3)
NH2CHO122, 10–112, 9 92260.189090.36 ± 0.024.41.67 ± 0.1934.70.03
NH2CHO169, 7–159, 6 380339.686060.36 ± 0.034.31.63 ± 0.3633.20.07(4)
NH2CHO168, 8–158, 7 329339.715190.30 ± 0.043.91.27 ± 0.3435.20.07(4)
NH2CHO167, 10–157, 9 284339.779540.36 ± 0.043.31.26 ± 0.2933.90.07(5)
NH2CHO166, 11–156, 10 246339.902500.29 ± 0.044.91.49 ± 0.4234.00.07(5)
NH2CHO163, 14–153, 13 166340.489630.37 ± 0.044.21.65 ± 0.3634.00.07
NH2CHO164, 13–154, 12 186340.534390.36 ± 0.045.21.98 ± 0.4434.10.07
NH2CHO164, 12–154, 11 186340.690740.46 ± 0.032.51.19 ± 0.2733.70.07
NH2CHO162, 14–152, 13 153349.478200.36 ± 0.043.61.41 ± 0.3333.90.08
NH2CHO92, 8–81, 7 58349.63403<0.30<1.30.08

Note. (1) Blend of four C2H5CN lines with similar spectroscopic constants. (2) Blend of two C2H5CN lines with similar spectroscopic constants. (3) Tentative detection. (4) Blend of four NH2CHO lines with similar spectroscopic constants. (5) Blend of two NH2CHO lines with similar spectroscopic constants.

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Table A9. Line Parameters for HCOOH, H2CCO, and c-C2H4O

MoleculeTransition Eu Frequency Tbr ΔV Tbr dV VLSR rmsNote
  (K)(GHz)(K)(km s−1)(K km s−1)(km s−1)(K) 
trans-HCOOH121, 12–111, 11 84257.975010.52 ± 0.025.53.00 ± 0.2334.50.03
trans-HCOOH154, 12–144, 11 181338.143840.42 ± 0.035.02.26 ± 0.4334.60.07
trans-HCOOH153, 13–143, 12 158338.201860.36 ± 0.034.41.70 ± 0.3934.70.07
trans-HCOOH154, 11–144, 10 181338.248820.35 ± 0.042.81.04 ± 0.2634.70.07
trans-HCOOH153, 12–143, 11 159340.229100.31 ± 0.045.81.92 ± 0.4935.10.07
cis-HCOOH130, 13–121, 12 95244.235100.33 ± 0.021.60.57 ± 0.0935.70.04
cis-HCOOH91, 9–80, 8 49244.247860.27 ± 0.022.50.73 ± 0.1634.20.04(1)
H2CCO124, 9–114, 8 284242.309380.12 ± 0.023.00.36 ± 0.1634.30.04(2)
H2CCO120, 12–110, 11 76242.375730.23 ± 0.024.00.99 ± 0.2733.80.04
H2CCO123, 10–113, 9 193242.398450.41 ± 0.033.11.35 ± 0.1934.40.04(2)
H2CCO122, 11–112, 10 128242.42466<0.10<0.40.04
H2CCO122, 10–112, 9 128242.536160.13 ± 0.023.20.43 ± 0.1935.50.04
H2CCO121, 11–111, 10 89244.712270.61 ± 0.033.42.24 ± 0.2034.40.04
H2CCO131,13–121, 12 100260.191980.67 ± 0.023.12.21 ± 0.1834.60.03
H2CCO171, 17–161, 16 160340.193080.41 ± 0.034.82.08 ± 0.6134.60.07(3)
c-C2H4O112, 10–101, 9 104338.771980.35 ± 0.034.21.57 ± 0.3534.60.07(4)

Note. (1) Partial blend with SO2. (2) Blend of two H2CCO lines with similar spectroscopic constants. (3) Partial blend with C2H5OH. (4) Blend of two c-C2H4O lines with similar spectroscopic constants.

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Appendix B: Fitted Spectra

Figures B1B11 show the results of the spectral line fitting (see Section 3.1 for details).

Figure B1.

Figure B1. ALMA spectra of the detected molecular emission lines. The blue lines represent fitted Gaussian profiles. For the molecules with multiple line detection, the spectra are sorted in ascending order of the upper state energy (the emission line with the lowest upper state energy is shown in the upper left panel and that with the highest energy is in the lower right panel). For SiO, the positions of primary and secondary peaks are indicated by arrows.

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Figure B2.

Figure B2. Same as in Figure B1 but for nitrogen-bearing molecules.

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Figure B3.

Figure B3. Same as in Figure B1 but for nitrogen-bearing molecules (continued).

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Figure B4.

Figure B4. Same as in Figure B1 but for sulfur-bearing molecules.

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Figure B5.

Figure B5. Same as in Figure B1 but for CH3OH.

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Figure B6.

Figure B6. Same as in Figure B1 but for CH3OH (continued) and 13CH3OH.

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Figure B7.

Figure B7. Same as in Figure B1 but for C2H5OH.

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Figure B8.

Figure B8. Same as in Figure B1 but for HCOOCH3.

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Figure B9.

Figure B9. Same as in Figure B1 but for HCOOCH3 (continued).

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Figure B10.

Figure B10. Same as in Figure B1 but for HCOOCH3 (continued), CH3OCH3, and CH3CHO.

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Figure B11.

Figure B11. Same as in Figure B1 but for HCOOH, H2CCO, and c-C2H4O.

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Footnotes

  • 6  
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  • 8  

    The following lines are used for non-LTE calculation with RADEX; H13CO+(3–2), HC18O+(4–3), H2CO(51,5–41,4), c-C3H2(32,1–21,2), CN(N = 3–2, ${\text{}}J=\tfrac{5}{2}\mbox{--}\tfrac{3}{2}$, ${\text{}}F=\tfrac{5}{2}\mbox{--}\tfrac{5}{2}$), H13CN(3–2), HC15N(3–2), HC3N(27–26), NO(${\text{}}J=\tfrac{7}{2}\mbox{--}\tfrac{5}{2}$, ${\rm{\Omega }}=\tfrac{1}{2}$, ${\text{}}F=\tfrac{9}{2}$ +$\tfrac{7}{2}$ ), CH3CN(140–130), SiO(6–5), CS(5–4), OCS(20–19), H2CS(71,6–61,5), SO(NJ =66–55), and CH3OH(75 E–65 E).

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10.3847/1538-4357/ac289b