JWST
/
MIRI Detection of a Carbon-rich Chemistry in the Disk of a Solar Nebula Analog
María José Colmenares
1
,
16
, Edwin A. Bergin
1
, Colette Salyk
2
, Klaus M. Pontoppidan
3
,
4
, Nicole Arulanantham
5
,
Jenny Calahan
6
, Andrea Banzatti
7
, Sean Andrews
6
, Geoffrey A. Blake
4
, Fred Ciesla
8
, Joel Green
5
, Feng Long
(
龙
凤
)
9
,
15
, Michiel Lambrechts
10
, Joan Najita
11
, Ilaria Pascucci
9
, Paola Pinilla
12
, Sebastiaan Krijt
13
,
Leon Trapman
14
and
the JDISCS Collaboration
1
Department of Astronomy, University of Michigan, 1085 South University Avenue, Ann Arbor, MI 48109, USA;
mjcolmen@umich.edu
2
Vassar College, 124 Raymond Avenue, Poughkeepsie, NY 12604, USA
3
Jet Propulsion Laboratory, California Institute of Technology, 4800 Oak Grove Drive, Pasadena, CA 91109, USA
4
Division of Geological and Planetary Sciences, California Institute of Technology, MC 150-21, 1200 E California Boulevard, Pasadena, CA 91125, USA
5
Space Telescope Science Institute, 3700 San Martin Drive, Baltimore, MD 21218, USA
6
Center for Astrophysics, Harvard & Smithsonian, 60 Garden Street, Cambridge, MA 02138, USA
7
Department of Physics, Texas State University, 749 North Comanche Street, San Marcos, TX 78666, USA
8
Dept. of the Geophysical Sciences, The University of Chicago, Chicago, IL 60637, USA
9
Lunar and Planetary Laboratory, University of Arizona, Tucson, AZ 85721, USA
15
10
Center for Star and Planet Formation and Natural History Museum of Denmark, Globe Institute, University of Copenhagen, Oster Voldgade 5-7, 1350 Cope
nhagen,
Denmark
11
NSFs NOIRLab, 950 N. Cherry Avenue, Tucson, AZ 85719, USA
12
Mullard Space Science Laboratory, University College London, Holmbury St Mary, Dorking, Surrey RH5 6NT, UK
13
School of Physics and Astronomy, University of Exeter, Stocker Road, Exeter, EX4 4QL, UK
14
Department of Astronomy, University of Wisconsin-Madison, 475 N Charter Street, Madison, WI 53706, USA
Received 2024 July 2; revised 2024 October 22; accepted 2024 October 23; published 2024 December 11
Abstract
It has been proposed, and con
fi
rmed by multiple observations, that disks around low-mass stars display a molecule-
rich emission and carbon-rich disk chemistry as compared to their hotter, more massive solar counterparts. In this
work, we present JWST Disk Infrared Spectral Chemistry Survey MIRI-MRS observations of the solar-mass star
DoAr 33, a low-accretion rate T Tauri star showing an exceptional carbon-rich inner disk. We report detections of
H
2
O, OH, and CO
2
, as well as the more complex hydrocarbons, C
2
H
2
and C
4
H
2
. Through the use of
thermochemical models, we explore different spatial distributions of carbon and oxygen across the inner disk and
compare the column densities and temperatures obtained from LTE slab model retrievals. We
fi
nd the best match to
the observed column densities with models that have carbon enrichment, and the retrieved emitting temperature
and area of C
2
H
2
with models that have C
/
O
=
2
–
4 inside the 500 K carbon-rich dust sublimation line. This
suggests that the origin of the carbon-rich chemistry is likely due to the sublimation of carbon-rich grains near the
soot line. This would be consistent with the presence of dust processing as indicated by the detection of crystalline
silicates. We propose that this long-lived hydrocarbon-rich chemistry observed around a solar-mass star is a
consequence of the unusually low M-star-like accretion rate of the central star, which lengthens the radial mixing
timescale of the inner disk, allowing the chemistry powered by carbon grain destruction to linger.
Uni
fi
ed Astronomy Thesaurus concepts:
Protoplanetary disks
(
1300
)
;
Astrochemistry
(
75
)
;
Planet formation
(
1241
)
1. Introduction
The predominant approach for understanding the connec-
tions between disk composition and the atmospheres of giant
planets relies on the elemental carbon-to-oxygen
(
C
/
O
)
ratio
(
K. I. Öberg et al.
2011b
; N. Madhusudhan
2012
)
.Ata
baseline level, the temperature-dependent condensation
sequence of volatile carriers of oxygen and carbon, such as CO,
CO
2
, and H
2
O, can lead to spatially varying C
/
O ratios in both
the gas and solid components
(
K. I. Öberg et al.
2011b
)
.
Beyond the CO snowline, the expectation is that all of the C
and O carriers reside mostly in the solids, frozen as icy mantles
atop dust grain cores. As dust grains move closer to the star and
cross the corresponding local snowlines, the icy mantles will
sublimate and alter the abundance of C and O in the gas. This
implies that the material available for planet formation will
change across the disk, potentially yielding a variety of planet
compositions.
However, a variety of mechanisms can in
fl
uence the gaseous
C
/
O ratio. For instance, extensive inward pebble drift can
supply abundant water ice to the inner disk. Once this water ice
sublimates it would substantially lower the gaseous inner disk
C
/
O ratio
(
R. A. Booth & J. D. Ilee
2019
; A. Banzatti et al.
2020
,
2023
)
. Extensive planetesimal formation and water
sequestration beyond the snowline should have the opposite
effect
(
raising inner disk gas-phase C
/
O; J. R. Najita et al.
2013
)
. The trapping of ices can also strongly in
fl
uence the C
/
O
ratio
(
N. F. W. Ligterink et al.
2024
)
. These concepts focus on
the most volatile and abundant components that are found as
molecular ices coating the more refractory solid grain cores,
which are themselves composed of solid-state organics and
The Astrophysical Journal,
977:173
(
24pp
)
, 2024 December 20
https:
//
doi.org
/
10.3847
/
1538-4357
/
ad8b4f
© 2024. The Author
(
s
)
. Published by the American Astronomical Society.
15
NASA Hubble Fellowship Program Sagan Fellow.
16
Corresponding author.
Original content from this work may be used under the terms
of the
Creative Commons Attribution 4.0 licence
. Any further
distribution of this work must maintain attribution to the author
(
s
)
and the title
of the work, journal citation and DOI.
1
silicate minerals
(
B. T. Draine
2011
)
. Closer to the star, within
1 au, there will exist additional dust sublimation fronts that
return this less volatile material to the gas. Of particular
importance for the composition of planets forming within this
region is the soot line. This is the theorized sublimation front of
carbonaceous organic material
(
M. E. Kress et al.
2010
)
that is
believed to activate near
∼
500 K
(
J. Li et al.
2021
)
. This
sublimation will
fl
ood the gas with carbon, elevating the local
gaseous C
/
O ratio while at the same time lowering C
/
O in the
solids. Interior to the soot line, this would lead to the formation
of rocky planets with reduced carbon content, such as the Earth
(
J. Li et al.
2021
)
. Beyond the soot line, it would facilitate the
formation of worlds with signi
fi
cant carbon inventories in their
mantles, which, through outgassing, would impact the nascent
atmospheric composition
(
E. A. Bergin et al.
2023
)
.
Within this context, spectroscopic surveys of protoplanetary
disks by the Spitzer Space Telescope
(
M. W. Werner et al.
2004
)
isolated a dichotomy where disks surrounding very low-
mass stars
(
<
0.2
M
e
)
have elevated C
2
H
2
/
HCN and
HCN
/
H
2
O
fl
ux ratios
(
I. Pascucci et al.
2009
,
2013
)
in
comparison to solar-mass T Tauri disks. This is suggested to be
the result of an increase in the gaseous C
/
O ratio in the
innermost regions close to the star
(
J. R. Najita et al.
2013
;
I. Pascucci et al.
2013
)
. Additional support for this dichotomy
has also been seen in recent spectra of disks surrounding very
low-mass stars obtained with the James Webb Space Telescope
(
JWST
)
. The disk around 2MASS-J160532-1933159
(
0.14
M
e
)
exhibits broad optically thick spectral features of
C
2
H
2
,
13
C
12
CH
2
, as well as detections of benzene
(
C
6
H
6
)
, and
C
4
H
2
(
B. Tabone et al.
2023
)
, also found in ISO-ChaI 147
(
A. M. Arabhavi et al.
2024
)
and Sz 28
(
J. Kanwar et al.
2024a
)
, along with emission from HC
3
N, C
3
H
4
, and C
2
H
6
.
Other than C
2
H
2
, these species were not isolated in Spitzer
spectra, and the chemistry surrounding these very low-mass
stars appears to be hydrocarbon dominated.
The origin of the hydrocarbon chemistry is uncertain. One
possibility is the destruction of carbon-rich organics near the
soot line. However, this points toward a conundrum: if this
chemistry is a result of carbon-rich grain destruction near
500 K, then these emission features should be prevalent
surrounding more luminous early-type stars, but they are not.
J. Mah et al.
(
2023
)
provide an alternative explanation. They
suggest that the supply of carbon-rich gas from the outer disk
may provide the fuel to generate hydrocarbons in the inner disk
gas. This is more prevalent in lower-mass stars, which have ice
lines that lie close to their stars where the viscous timescales
are shorter, in addition to the radial drift of particles being more
ef
fi
cient
(
P. Pinilla et al.
2013
)
. This scenario was proposed to
explain the spectrum of Sz 114, which showed strong water
emission lines despite having the same stellar mass as J160532-
1933159, likely due to the difference in their pebble disks
(
C. Xie et al.
2023
)
. Alternatively, C. Walsh et al.
(
2015
)
propose that a combination of weak far-ultraviolet
(
FUV
)
and
X-ray-driven chemistry in M dwarf disks is the cause of
abundant C
2
H
2
and HCN observed in the atmosphere of
the disk.
With the idea that carbon-rich chemistry so far has been
expected to be dominant in low-mass stars, in this work, we
present JWST MIRI observations of the hydrocarbon-rich
source, DoAr 33, a 1.1
M
e
star. We detect the emission of H
2
O,
CO
2
, OH, and C
2
H
2
, including its isotopologue
13
C
12
CH
2
,
C
4
H
2
, and tentatively CH
4
and HC
3
N, for all of which we
retrieve column densities, temperatures, and emitting areas, as
described in Section
2
. With the objective of disentangling the
origin of a rich carbon and oxygen chemistry in the inner disk
of solar analogs, in Section
3
we introduce thermochemical
models with varying abundances of the main carbon and
oxygen carriers. We calculate abundances, column densities,
and
fl
ux-weighted temperatures for comparison with the
detected molecules in Section
4
. We then discuss
(
Section
5
)
how DoAr 33 may shed important light on the origin of the
hydrocarbon dichotomy found within disks surrounding solar-
mass and very low-mass stars.
2. Observations and Retrievals
2.1. Observations and Data Reduction
We present JWST
(
J. Rigby et al.
2023
)
, MIRI
(
G. S. Wright
et al.
2023
)
, MRS
(
M. Wells et al.
2015
; I. Argyriou et al.
2023
)
observations of DoAr 33, observed as a part of the JWST
Cycle 1 GO1584 program
(
PIs C. Salyk and K. Pontoppidan
)
,
and the JWST Disk Infrared Spectral Chemistry Survey
(
JDISCS; K. M. Pontoppidan et al.
2024
)
. The properties of
DoAr 33 are listed in Table
1
. This source was acquired by
JWST using the MRS target acquisition procedure along with
the neutral density
fi
lter. We used the four-point dither pattern
in the negative direction and observed in all three MIRI-MRS
grating settings such that we had full spectral coverage
(
4.9
–
28
μ
m
)
. The exposure time per module was set to
1687.224 s in order to achieve a signal-to-noise ratio
∼
100 at
the longest wavelengths.
The spectrum was reduced with the standard JDISCS
reduction pipeline, explained in detail in K. M. Pontoppidan
et al.
(
2024
)
. This custom pipeline produces a higher spectral
contrast than the standard JWST pipeline by using observations
of asteroids as spectral response function calibrators, which
produces a higher signal-to-noise ratio for Channels 3 and 4
when compared to a traditional calibration using stars. In the
case of DoAr 33, the 1.15.0 version of the JWST Calibration
Pipeline
(
H. Bushouse et al.
2024
)
and the jwst_1253.pmap
Calibration Reference Data System context was used. The
reduced spectrum is shown in Figure
1
. The process to compute
the continuum involves an iterative procedure as described in
K. M. Pontoppidan et al.
(
2024
)
. This method begins by
applying a median
fi
lter to the spectrum to smooth it out and
then comparing it with past iterations. During each iteration,
wavelength channels exhibiting a lower
fl
ux density than the
previous iteration are kept, while rejected ones are replaced
through linear interpolation; a second-order Savitzky
–
Golay
fi
lter is utilized to further smooth the result. The regions
13.4
–
14.1
μ
m and 14.95
–
15
μ
m are excluded from the
continuum calculation to avoid overestimation because broad
molecular features from the
Q
branch of organic molecules
produce a pseudocontinuum.
2.2. LTE Slab Model Retrievals
To benchmark the thermochemical models of DoAr 33, we
fi
rst retrieve best-
fi
t column densities, temperatures, and
emitting areas for each detected molecule using the local
thermal equilibrium
(
LTE
)
slab models in
spectools
_
ir
(
C. Salyk
2022
)
. These models assume an isothermal slab of
gas that can be characterized by only its temperature, line-of-
sight column density, and emitting area. The emitting area can
be interpreted as a circle of radius
R
slab
, in which case an
2
The Astrophysical Journal,
977:173
(
24pp
)
, 2024 December 20
Colmenares et al.
emitting radius can be obtained by assuming
p
=
A
R
slab
2
.
However, the emission may instead arise from one or more
rings with total area
A
. The code uses the line parameters from
the HITRAN database
(
I. E. Gordon et al.
2022
)
to model the
emission spectra of different molecules, allowing us to directly
compare to the observations. The code takes into account
mutual line overlap, which has been shown to cause saturation
in regions of dense line clustering for the organics
(
B. Tabone
et al.
2023
)
and in ortho
–
para line pairs for water
(
A. Banzatti
et al.
2024
)
. Despite their simplicity, LTE models have been
able to successfully reproduce infrared molecular spectra
observed with Spitzer
(
e.g., J. S. Carr & J. R. Najita
2011
;
C. Salyk et al.
2011
)
and more recently JWST
(
e.g., D. Gasman
et al.
2023
; C. Xie et al.
2023
; C. E. Muñoz-Romero et al.
2024
; M. Temmink et al.
2024a
)
.
We follow a procedure similar to previous works
(
C. Salyk
et al.
2011
; S. L. Grant et al.
2023
)
to obtain the parameters
from the slab models. We run a grid of slab models with
N
col
=
10
14
–
10
22
cm
−
2
in steps of
=
N
log
0.166
col
and
T
slab
=
100
–
1500 K in steps of 25 K. These models are
generated within the spectral window of 12
–
16.5
μ
m and then
compared with the MRS spectrum through a
χ
2
minimization.
The only exception is the OH models, which are run until
T
slab
=
3000 K and within a window of 12
–
28
μ
m to maximize
the amount of features included in the
fi
t. We convolve the
models at each wavelength to the corresponding MIRI-MRS
resolving power by adopting the spectral resolution measured
by K. M. Pontoppidan et al.
(
2024
)
, which, in the spectral range
considered, is in agreement with previous measurements
(
A. Labiano et al.
2021
; O. C. Jones et al.
2023
)
. Then, we
select a spectral window for each molecule to calculate the
reduced
χ
2
and
fi
nd the best-
fi
t parameters. The details of the
χ
2
calculation are explained in Appendix
D
, and the spectral
ranges used to calculate it are shown in Figures
18
and
19
. For
each column density and temperature pair in the grid, we adjust
the emitting area to minimize
χ
2
for that pair. Then, we
fi
nd the
lowest of those
χ
2
values among the pairs in the grid. The
resulting
χ
2
maps for each molecule can be found in
Appendix
D
.
Molecules like C
2
H
2
, HCN, H
2
O and OH have a signi
fi
cant
amount of overlap in their emission; therefore, we implement
an additional step to further isolate their emission. First, we
fi
nd
the best-
fi
t model for H
2
O. Then, prior to simulating CO
2
,we
subtract the best-
fi
tH
2
O model to eliminate interfering features
that could in
fl
uence the
fi
tting. Similarly, we subtract the best
CO
2
model from the residual spectrum before
fi
tting the rest of
the molecules. This ensures that we are only taking into
account the most signi
fi
cant feature of each species. In the case
of C
2
H
2
, we simultaneously
fi
t its spectrum with
13
C
12
CH
2
and
HCN due to the overlap in wavelength of their emission
features. We test all possible combinations of column densities
and temperatures within the speci
fi
ed grid, allowing the values
to vary independently. We report the parameters of the best-
fi
t
models for each molecule in Table
2
, and we show the
fi
t of the
13
–
16.5
μ
m region in Figure
2
. The individual models, along
with the residuals, are shown in Figures
18
and
19
.
In the case of H
2
O, we only focus on the rotational
transitions detected around 13
–
16.5
μ
m, for which we found a
single component with
T
=
600 K,
= ́
-
N
310cm
HO
18
2
2
and
R
slab
=
0.27 auis able to reproduce the features. More detailed
Figure 1.
JWST MIRI-MRS spectrum of DoAr 33. The insets show isolated emission features of some of the molecules detected, and the calculated continuum is
shown as a pink line. Most of the unmarked emission lines correspond to water vapor. We discuss the presence of dust emission features in Appendix
A
.
Table 1
Stellar and Disk Properties of DoAr 33
Property
Value
Reference
Spectral type
K4
J. Bouvier & I. Appenzeller
(
1992
)
Distance
139 pc
Gaia Collaboration et al.
(
2018
)
T
eff
4467 K
S. M. Andrews et al.
(
2010
)
Luminosity
1.5
L
e
S. M. Andrews et al.
(
2010
)
Mass
1.1
M
e
S. M. Andrews et al.
(
2018
)
Inclination
41
°
.8
J. Huang et al.
(
2018
)
Accretion rate 2.52
×
10
−
10
M
e
yr
−
1
L. A. Cieza et al.
(
2010
)
3
The Astrophysical Journal,
977:173
(
24pp
)
, 2024 December 20
Colmenares et al.
modeling, including more than one temperature component or a
temperature gradient, could be implemented to simultaneously
fi
t for the rotational transitions across the MIRI bandpass
(
A. Banzatti et al.
2023
; C. E. Muñoz-Romero et al.
2024
;
K. R. Schwarz et al.
2024
; M. Temmink et al.
2024b
)
;
however, this lies beyond the scope of this work. The water
rotational emission is believed to arise from larger disk radii
than for the vibrational mode emission
(
D. Gasman et al.
2023
)
; therefore, this approach allows us to isolate water
emission that is cospatial with that of the organics in the
inner disk.
We
fi
t the
Q
branch of C
2
H
2
and
13
C
12
CH
2
at
∼
13.7
μ
m
while limiting the emitting area and temperature of both species
to be the same. We
fi
nd that models with
=
T
500
CH
22
K,
R
slab
=
0.17 au,
=
N
10
CH
17
22
cm
−
2
, and C
2
H
2
/
13
C
12
CH
2
=
4.64 are able to reproduce the full acetylene feature. Given the
local interstellar medium
12
C
/
13
C ratio of 68, this suggests that
12
C
2
H
2
emission is optically thick, although not optically thick
enough to blend into a pseudocontinuum as observed in other
carbon-rich sources
(
B. Tabone et al.
2023
)
. Because of this
and the large degeneracies that are present when simulta-
neously
fi
tting three species, we determine the actual C
2
H
2
column from
13
C
12
CH
2
with an assumed isotopic ratio. We
discuss this further in Section
4.2
.
We also detect the presence of rotational lines of OH, which
we
fi
t across a larger wavelength range to obtain a better
constraint of the parameters. The regions used for the
χ
2
fi
t are
shown shaded in Figure
18
. The best-
fi
t temperature,
T
OH
=
950 K, is higher than that of water
(
=
T
600
HO
2
K
)
,
with a low column density of
N
OH
=
3
×
10
14
cm
−
2
. Despite its
relatively high
fl
ux at longer wavelengths, the column density
and temperature have large uncertainties. We also checked for
the presence of lines due to prompt emission between 10 and
12
μ
m caused by UV photodissociation of water
(
J. R. Najita
et al.
2010
)
. For reference, we created a high-temperature
(
6000 K
)
OH slab model, which we show in the top panel of
Figure
19
. The insets show that some of the lines between 10
and 12
μ
m show the
Λ
-doublet asymmetry previously observed
with Spitzer
(
J. S. Carr & J. R. Najita
2014
)
and predicted by
B. Tabone et al.
(
2021
,
2024
)
, indicative of prompt emission.
These features are very weak compared to the thermal OH
observed at longer wavelengths, suggesting that this source has
a low UV
fi
eld.
In the case of diacetylene
(
C
4
H
2
)
, we only detect emission
from the
Q
branch at
∼
15.9
μ
m, which we are able to
fi
t
with a model with
= ́
N
210
CH
15
42
cm
−
2
,
T
=
150 K, and
R
slab
=
1.36 au. We also explored models where we
fi
xed the
temperature and emitting area to the one found for C
2
H
2
. This
is discussed further in Section
4.3.1
. We also report a tentative
detection of methane
(
CH
4
)
at
∼
7.65
μ
m and HC
3
Nat
∼
15.07
μ
m, which we further discuss in Section
5.5
. We also
detect the presence of CO emission around 5
μ
m; however,
because these features are from optically thin transitions at high
energy levels
(
e.g., M. Temmink et al.
2024a
)
, they cannot be
used to determine the CO column density.
3. Methods
3.1. Disk Modeling
For modeling the disk, we used the Dust and Lines
(
DALI
)
thermochemical code
(
S. Bruderer et al.
2012
; S. Bruderer
2013
)
, with the extensions implemented by A. D. Bosman et al.
(
2022b
)
to reproduce the inner disk regions more accurately.
Figure 2.
Continuum-subtracted spectrum and best-
fi
t slab models for the molecules detected. The data were offset vertically for clarity. The pink-shaded region
shows the composite model of C
2
H
2
,
13
C
12
CH
2
, HCN, CO
2
,H
2
O, C
4
H
2
, and HC
3
N. We show a closer look at the HC
3
N feature in Figure
12
.
Table 2
Best-
fi
t Parameters from the Slab Models
Molecule
log
N
col
T
slab
R
slab
(
cm
−
2
)(
K
)(
au
)
H
2
O
18.5
-
+
0.3
0.
4
600
-
+
85
10
6
0.27
CO
2
17.8
-
+
0.5
1.0
200
-
+
57
65
0.77
C
2
H
2
a
17.0
-
+
0.3
0.3
500
-
+
74
87
0.17
13
C
12
CH
2
b
16.3
(
500
)(
0.17
)
HCN
14.0
600
3.99
C
4
H
2
15.3
150
1.36
OH
14.5
950
1.14
Note.
The uncertainties are reported only for cases with a closed 1
σ
contour,
based on Figure
17
.
(
a
)
This column is uncertain; see Section
4
for a discussion.
(
b
)
The emitting area and temperature are
fi
xed to that of C
2
H
2
during the
fi
tting.
4
The Astrophysical Journal,
977:173
(
24pp
)
, 2024 December 20
Colmenares et al.
These extensions include the increased formation of H
2
, water
UV shielding, and dissociation heating
(
A. E. Glassgold &
J. R. Najita
2015
)
. As DoAr 33 shares a similar spectral type
classi
fi
cation
(
K4
)
with AS 209
(
K5
)
, we use the AS 209 stellar
spectrum from K. Zhang et al.
(
2021
)
. The UV emission,
generated by accretion
(
E. Gullbring et al.
2000
)
,isan
important driver of the surface chemistry in low-mass T Tauri
systems
(
P. Woitke et al.
2009
; I. Kamp et al.
2024
)
. Based on
the lower accretion rate of DoAr 33
(
2.5
×
10
−
10
M
e
yr
−
1
)
compared to AS 209
(
5
×
10
−
8
M
e
yr
−
1
)
, we decreased the
FUV emission by a factor of
∼
100 to account for the difference
in accretion rates between the two sources. The low UV
fl
ux is
consistent with the lack of prompt OH emission due to H
2
O
photodissociation, as discussed in Section
2.2
. We show the
spectra of both sources in Figure
15
.
In terms of the physical structure of the disk, we consider a
viscous accretion disk
(
D. Lynden-Bell & J. E. Pringle
1974
)
that follows the form
()
⎜⎟⎜⎟
⎛
⎝
⎞
⎠
⎡
⎣
⎢
⎛
⎝
⎞
⎠
⎤
⎦
⎥
S=S
-
gg
--
R
R
R
R
exp
,
1
c
cc
gas
2
where
Σ
gas
is the surface density of the gas,
R
c
is the critical
radius,
Σ
c
is the surface density at
R
c
, and
γ
is the power-law
slope. The scale height angle is de
fi
ned by
()
⎜⎟
⎛
⎝
⎞
⎠
=
y
hh
r
R
,2
c
c
where
ψ
is the
fl
aring angle, and the physical scale height is
H
(
r
)
∼
rh
. We include two different dust populations made up
of small
(
0.005
–
1
μ
m
)
and large
(
0.005
–
1000
μ
m
)
dust grains,
distributed in the disk according to
()
()
()
()
⎜⎟
⎡
⎣
⎢
⎛
⎝
⎞
⎠
⎤
⎦
⎥
r
p
=
-S
-
f
Hr
z
Hr
1
2
exp
1
2
3
dust,small
dust
2
()
()
()
⎜⎟
⎡
⎣
⎢
⎛
⎝
⎞
⎠
⎤
⎦
⎥
r
pc
c
=
S
-
f
Hr
z
Hr
2
exp
1
2
.4
dust,large
dust
2
Here,
Σ
dust
is the surface density of small and large dust,
f
is
the large dust fraction, and
χ
describes the settling of large
dust. The values for all of the parameters used can be found in
Table
3
. The opacities of both populations follow the DSHARP
opacities
(
T. Birnstiel et al.
2018
)
used by K. Zhang et al.
(
2021
)
. The photometry of DoAr 33 shows an emission bump
around
∼
100
μ
m
(
Y. Liu et al.
2022
)
. In order to reproduce this
feature, we increased the scale height of the large dust outside
10 au. This effectively mimics a wall of dust, consistent with
the gap substructure at
∼
9 au inferred from millimeter
observations of the source
(
J. Huang et al.
2018
)
. Our spectral
energy distribution
(
SED
)
-
fi
tting procedure is further explained
in Appendix
C
. The resulting 2D gas and dust density pro
fi
les
are shown in Figure
3.
In order to properly model the full hydrocarbon chemistry
and include the relevant species, we use an expanded chemical
network as presented in S. E. Duval et al.
(
2022
)
. The original
network follows that implemented by C. Walsh et al.
(
2015
)
,
with the modi
fi
cations added by A. D. Bosman et al.
(
2022b
)
.
We also vary the initial abundances in the disk in order to
mimic the environment of an elevated C
/
O ratio. We have two
different scenarios that give rise to a change in C
/
O: an excess
of CH
4
or an excess of CH
4
accompanied by H
2
O depletion.
At the same time, in order to explore the origin of excess
carbon, we apply the changes in abundances to two regions:
inside a dust temperature of
T
dust
=
250 K or inside of
T
dust
=
500 K. The latter temperature has been argued to be
associated with the sublimation of carbon-rich grains at the
“
soot line
”
by J. Li et al.
(
2021
)
. This is a process that would
locally elevate the C
/
O ratio as carbon grains carry
∼
50% of
elemental carbon in the interstellar medium
(
ISM; A. Mishra &
A. Li
2015
; E. A. Bergin et al.
2015
)
. These two setups will
allow us to differentiate between a scenario where the excess
carbon is produced due to the sublimation of carbon grains at
the soot line
(
500 K model
)
, which would happen in the inner
disk, therefore resulting in high temperatures and a scenario
where the carbon is sublimated off icy grains in the outer disk
and then transported inward via advection resulting in a more
Table 3
Thermochemical Model Parameters
Parameter
Symbol
Value
Critical radius
R
c
20 au
Gas surf. dens. at
R
c
Σ
c
13 g cm
−
2
Surf. dens. power-law slope
γ
0.9
Disk opening angle
h
c
0.045
Disk
fl
aring angle
ψ
0.08
Large dust fraction
f
0.999
Large dust settling
χ
0.1 for
r
10 au
0.8 for
r
>
10 au
Figure 3.
Gas
(
top
)
and dust
(
bottom
)
density pro
fi
les from the thermochemical
models. The orange line in the bottom plot shows the continuum
τ
=
1 line at
15
μ
m. Inside 10 au, the large dust population is mostly settled in the midplane.
5
The Astrophysical Journal,
977:173
(
24pp
)
, 2024 December 20
Colmenares et al.
spatially extended distribution with overall lower temperatures
(
250 K models
)
. This would be roughly consistent with the
model of the origin of hydrocarbon-rich chemistry suggested
by J. Mah et al.
(
2023
)
. Outside of the 250 K and 500 K
regions, the abundances of carbon and oxygen carriers are set
so that the C
/
O ratio is solar. As a standard for comparison, we
also include a model with solar abundance everywhere in the
disk. This results in a grid of 19 models, for which we indicate
the names and abundances considered in Table
4
.
In this work, we refrain from comparing the observations to
simulated spectra, in part due to the uncertainty that can arise
from accounting for mutual line overlap, which can be
signi
fi
cant for molecules like C
2
H
2
, as demonstrated in
B. Tabone et al.
(
2023
)
. But, more importantly, we aim to
focus on the retrieved outputs from the data, rather than on the
details of the radiative transfer. Therefore, we will compare to
column densities, emitting areas, and
fl
ux-weighted tempera-
tures
(
discussed below
)
. This reduces the time required to
forward model this source using complex thermochemical
models. This solution should approximate the key effects and
enable a direct exploration of why DoAr 33 is a rare K star
exhibiting rich hydrocarbon emission.
3.2. Flux-weighted Temperatures
Column density estimates derived from observations can
intrinsically reduce the uncertainty arising from not knowing
how the gas is distributed vertically in the disk since they are
integrated along the line of sight; therefore, they can be directly
compared to the column densities calculated in the thermo-
chemical models, without having to match a 2D gas
distribution. This is not the case for the emitting temperature,
which requires that we consider where in the disk this emission
is coming from. From the thermochemical models, we are able
to obtain a 2D temperature distribution for both the gas and the
dust components; we show these distributions in Figure
4
.
However, in order to compare to the estimates from the slab
models, we must calculate a representative value for each
molecule in the thermochemical models. Here, we describe the
procedure we applied to condense the 2D temperature
structures into a single emitting temperature.
In the LTE slab models, the temperature retrieved for each
species is a representative temperature at which the gas we can
observe is emitting. In order to draw a similar parallel, we make
use of contribution functions, which trace where in the disk an
emission line is formed. Once the necessary information about
energy levels, statistical weights, and Einstein A coef
fi
cients is
provided to DALI in the form of LAMDA
17
fi
les
(
F. L. Schöier
et al.
2005
)
, the code is able to perform excitation calculations
for any given molecule included in the chemical network. With
this information, we can calculate the 2D contribution function
of a speci
fi
ed transition
(
S. Bruderer et al.
2012
)
to understand
where it is originating physically. It is important to note that the
region where a speci
fi
c line is generated does not necessarily
correspond to the region where that species is most abundant
due to, e.g., the effects of optical depth. Therefore, this method
allows us to mimic an emitted temperature instead of a
temperature simply weighted by abundance. In the case of
C
2
H
2
, the spectroscopic information for the LAMDA
fi
le was
compiled based on the ExoMol database
(
K. L. Chubb et al.
2020
)
.
In practice, we select a speci
fi
c transition for each of the
species observed in the MIRI spectrum and calculate its
contribution function in DALI. To select the transition, we use
the spectral line analysis tool
iSLAT
18
(
E. Jellison et al.
2024
)
,
which takes line transition information from HITRAN
(
I. E. Gordon et al.
2022
)
. This tool allows us to input the
parameters obtained from the
fi
tting of slab models and
generate a synthetic spectrum. Once the spectrum is generated,
a spectral range can be selected for which the strongest line
transition is shown. We then select the strongest transition of
each molecule in the spectral range between 12 and 17
μ
m for
which we calculate the contribution function using DALI. The
selected transitions are indicated in Table
5
and plotted for the
Table 4
Input Abundances of the Thermochemical Models Inside the 250 K and 500 K Contours
Name
Total C
Total O
C
/
OH
2
OCOCO
2
CH
4
Solar
5.00
×
10
−
5
1.44
×
10
−
4
0.47
1.20
×
10
−
4
8.50
×
10
−
5
4.15
×
10
−
5
8.50
×
10
−
6
ch4_excess_co_1_t500
2.03
×
10
−
4
4.50
×
10
−
4
1
1.20
×
10
−
4
8.50
×
10
−
5
4.15
×
10
−
5
1.62
×
10
−
4
ch4_excess_co_2_t500
4.91
×
10
−
4
1.02
×
10
−
3
2
1.20
×
10
−
4
8.50
×
10
−
5
4.15
×
10
−
5
4.49
×
10
−
4
ch4_excess_co_1_t250
2.03
×
10
−
4
4.50
×
10
−
4
1
1.20
×
10
−
4
8.50
×
10
−
5
4.15
×
10
−
5
1.62
×
10
−
4
ch4_excess_co_2_t250
4.91
×
10
−
4
1.02
×
10
−
3
2
1.20
×
10
−
4
8.50
×
10
−
5
4.15
×
10
−
5
4.49
×
10
−
4
co_dep_co_1_t500
1.20
×
10
−
4
2.49
×
10
−
4
1
1.20
×
10
−
4
8.50
×
10
−
6
0
1.20
×
10
−
4
co_dep_co_2_t500
2.49
×
10
−
4
5.06
×
10
−
4
2
1.20
×
10
−
4
8.50
×
10
−
6
0
2.49
×
10
−
4
co_dep_co_4_t500
5.06
×
10
−
4
1.02
×
10
−
3
4
1.20
×
10
−
4
8.50
×
10
−
6
0
5.06
×
10
−
4
co_dep_co_1_t250
1.20
×
10
−
4
2.49
×
10
−
4
1
1.20
×
10
−
4
8.50
×
10
−
6
0
1.20
×
10
−
4
co_dep_co_2_t250
2.49
×
10
−
4
5.06
×
10
−
4
2
1.20
×
10
−
4
8.50
×
10
−
6
0
2.49
×
10
−
4
co_dep_co_4_t250
5.06
×
10
−
4
1.02
×
10
−
3
4
1.20
×
10
−
4
8.50
×
10
−
6
0
5.06
×
10
−
4
co_water_dep_co_1_t500
1.20
×
10
−
5
3.25
×
10
−
5
1
1.20
×
10
−
5
8.50
×
10
−
6
0
1.20
×
10
−
5
co_water_dep_co_2_t500
3.25
×
10
−
5
7.35
×
10
−
5
2
1.20
×
10
−
5
8.50
×
10
−
6
0
3.25
×
10
−
5
co_water_dep_co_4_t500
7.35
×
10
−
5
1.56
×
10
−
4
3
1.20
×
10
−
5
8.50
×
10
−
6
0
7.35
×
10
−
5
co_water_dep_co_1_t250
1.20
×
10
−
5
3.25
×
10
−
5
1
1.20
×
10
−
5
8.50
×
10
−
6
0
1.20
×
10
−
5
co_water_dep_co_2_t250
3.25
×
10
−
5
7.35
×
10
−
5
2
1.20
×
10
−
5
8.50
×
10
−
6
0
3.25
×
10
−
5
co_water_dep_co_4_t250
7.35
×
10
−
5
1.56
×
10
−
4
4
1.20
×
10
−
5
8.50
×
10
−
6
0
7.35
×
10
−
5
water_dep_no_co
8.50
×
10
−
5
2.55
×
10
−
4
1.75
1.20
×
10
−
5
8.50
×
10
−
5
0
8.50
×
10
−
5
water_dep_co
1.13
×
10
−
4
2.55
×
10
−
4
1.36
1.20
×
10
−
5
5.67
×
10
−
5
2.83
×
10
−
5
8.50
×
10
−
5
Note.
The abundances are reported with respect to H.
17
https:
//
home.strw.leidenuniv.nl
/~
moldata
/
18
https:
//
github.com
/
spexod
/
iSLAT
6
The Astrophysical Journal,
977:173
(
24pp
)
, 2024 December 20
Colmenares et al.
solar model in Figure
4
. We map these contribution functions
to the gas temperature in the disk model and calculate a single
contribution function-weighted temperature for each model.
These temperatures are discussed in Section
4
, where we
compare them to the temperatures derived from slab models.
4. Results
The thermochemical modeling process returns 2D distribu-
tions of abundances in the disk for all of the species included in
the chemical network. Here, we only focus on the oxygen and
carbon carriers that are detected in the MIRI-MRS spectrum of
DoAr 33. In order to directly compare the modeling products to
the parameters retrieved from the LTE slab models, we
compute column densities and
fl
ux-weighted temperatures for
all of the models described in Table
4
based on the abundance
maps. We calculated the radial distributions of column
densities by vertically integrating the abundance from the
surface of the disk down to the
τ
=
1 surface at 15
μ
m
(
shown
as an orange line in Figure
3
)
. For the contribution function-
weighted temperature, we followed the procedure outlined in
Section
3.2
In Sections
4.1
–
4.3
, we individually discuss the results for
each molecule. We include all of the abundance maps for H
2
O,
CO
2
, and C
2
H
2
in Appendix
E
. To make the analysis more
tractable, we did not include HCN and HC
3
N and did not
attempt to match the retrieved columns for these species.
4.1. H
2
O, CO
2
, and OH
In the top left panel of Figure
5
, we show the column density
of water as a function of radius for all of the models, colored
according to the C
/
O ratio assumed. The line styles indicate
whether we assume the increased C
/
O is a product of only
carbon enhancement or the combination of carbon enhance-
ment and oxygen depletion, and we include a model with solar
abundances for comparison.
The solar abundance model predicts the overall highest
column density for water, which then decreases beyond 1 au.
The high column density of the solar abundance model appears
to be inconsistent with the reference values retrieved through
the LTE slab models
(
Table
2
)
. In fact, all of the models that
consider the default water abundance of
∼
10
−
4
, shown in solid
lines, overpredict the column density of water. Only the models
where we include water depletion are able to match the water
column. However, there are several important caveats to
determining an overall water abundance through column
densities. For one, we do not model the entire water spectrum,
and therefore, the
fi
t results reported for water in Table
2
are
only approximately valid
(
see A. Banzatti et al.
2023
;
D. Gasman et al.
2023
; C. E. Muñoz-Romero et al.
2024
)
.
We note that the retrieved water column is consistent with
values obtained for other full disks like GW Lup
(
S. L. Grant
et al.
2023
)
and FZ Tau
(
K. M. Pontoppidan et al.
2024
)
, but in
this latter disk, the retrieved water column of
∼
10
18
cm
−
2
was
found to be consistent with solar abundances. In our case, the
models with the canonical water abundance of
∼
10
−
4
predict
columns closer to 10
20
cm
−
2
. This discrepancy could be, in
part, because some of the columns we modeled might not have
the right temperature for IR emission, as has been noted by
R. Meijerink et al.
(
2009
)
and A. D. Bosman et al.
(
2022a
)
. The
modeled columns depend on how far into the disk we assume
we can see, which is highly dependent on the gas-to-dust ratio.
In our models, the water emission is arising from material with
a gas
/
dust ratio of
∼
10
5
, which is consistent with previous
fi
ndings of a well-settled dust disk
(
Y. Liu et al.
2012
)
.Itis
possible that a potential solution to the water column issue
(
e.g., R. Meijerink et al.
2009
)
is a lower hydrogen column,
which would also have implications for the overall carbon
chemistry. This is explored in Section
5.2
. Stronger observa-
tional constraints on the total gas and dust content are needed to
be able to model the water column more accurately.
We then examined the column densities of the second most
signi
fi
cant oxygen tracer in the MIRI spectrum, CO
2
. In the top
right panel of Figure
5
, we show the column densities
calculated for this molecule. In contrast to water, the column
density of this molecule is highest around 1 au. Both H
2
O and
CO
2
share the same precursor, OH. A. D. Bosman et al.
(
2022b
)
and S. E. Duval et al.
(
2022
)
suggested that CO
2
formation in the warm
(
>
400 K
)
gas is curtailed as OH is more
Figure 4.
Gas
(
top
)
and dust
(
bottom
)
temperature pro
fi
les from the
thermochemical models. The colored contours in the top
fi
gure represent the
contribution functions for the
water
_
dep
_
co
model
(
see Table
4
)
, where
90% of the emission is produced. The transitions for each molecule are
indicated in Table
5
. The lines in the bottom plot represent the 250 K and
500 K contours, inside of which we change the abundances to increase the C
/
O
ratio.
Table 5
Strongest Line Transitions in the 12
–
16
μ
m Region for Best-
fi
t Slab Model
Parameters
Species
Einstein A Coeff.
E
u
Wavelength
(
s
−
1
)(
K
)(
μ
m
)
H
2
O
3.48
3950.8
14.2096
CO
2
1.54
1113.3
14.9777
C
2
H
2
6.06
1358.3
13.6992
7
The Astrophysical Journal,
977:173
(
24pp
)
, 2024 December 20
Colmenares et al.
likely to react with H
2
than CO. The models are only able to
reproduce the column density retrieved from slab models in the
zone around 1 au. For reference, the emitting area estimated
from the slab models is shown as a shaded annulus of the same
area. This indicates that the CO
2
emission is likely coming
from a ring of gas around 1 au. One implication of this result is
that it would suggest that CO
2
emission would trace cooler gas
than regions with abundant water vapor, which has been found
in some instances via analysis of JWST spectra
(
C. Xie et al.
2023
; D. Gasman et al.
2023
)
.
In the bottom left panel of Figure
5
, we compared the
retrieved OH column density. As expected, the models with a
lower C
/
O ratio produce the highest OH columns. More
speci
fi
cally, the model with a solar C
/
O ratio predicts a column
of almost 10
18
cm
−
2
, much higher than the retrieved best
fi
tof
3
×
10
14
cm
−
2
. Nonetheless, the uncertainty of the column
density does not allow us to rule out C
/
O
=
1, pointing more
toward a C
/
O
1. We note that despite the weak prompt
emission at shorter wavelengths, OH emission may not be in
non-LTE
(
see discussion for H
2
O by B. Tabone et al.
2021
)
;
therefore, the best-
fi
t parameters from the LTE models might
not fully represent the local gas properties.
In Figure
6
, we show the model emitting temperatures for
C
2
H
2
,CO
2
, and H
2
O, along with the estimate from the slab
model
fi
tting. We show only the water depletion scenarios
since they are consistent with the water column densities from
the slab models. Overall, the thermochemical models predict
water has the highest temperature, and CO
2
has the lowest,
which is consistent with the expectation from the slab model
retrievals from observations. Nonetheless, the CO
2
and H
2
O
temperatures do not allow us to differentiate between the two
different carbon enhancement scenarios proposed
(
see
Section
3.1
)
.
4.2. C
2
H
2
and
13
C
12
CH
2
As mentioned in Section
2.2
, in order to derive the actual
C
2
H
2
column, we assume an isotopic ratio. This ratio is
unknown, and B. Tabone et al.
(
2023
)
assumed 35 based on the
models of P. M. Woods & K. Willacy
(
2009
)
. We adopt this
value and report the C
2
H
2
column density to be
́
N
3
5
CCH
13 12
2
,
which results in
= ́
-
N
7.5 10 cm
CH
17
2
22
. We note this value
could be substantially higher as the
12
C
/
13
C ratio of
hydrocarbons and nitriles in the outer disk of TW Hya is
closer to the interstellar value
(
P. Hily-Blant et al.
2019
;
Figure 5.
Column density for H
2
O, CO
2
, and C
2
H
2
as a function of radius for the models in Table
4
. The color bar re
fl
ects the value of C
/
O for each model, and the
linestyle indicates the method for increasing the C
/
O ratio. The dashed
–
dotted horizontal line shows the best-
fi
t value found from LTE slab models, along with the
shaded 1
σ
uncertainty. The shaded gray vertical region corresponds to the emitting area estimated from slab models. In the case of CO
2
, we assumed this value to be
an annulus of the same area instead of a continuous distribution, and we placed the ring where it best matched the thermochemical models.
8
The Astrophysical Journal,
977:173
(
24pp
)
, 2024 December 20
Colmenares et al.
E. A. Bergin et al.
2024
; T. C. Yoshida et al.
2024
)
. Therefore,
the uncertainties of the C
2
H
2
column shown in Figure
5
stem
from assuming
12
C
/
13
C can go from
≈
5, as directly retrieved
from slab models to 68, the interstellar value.
From the thermochemical models, it is clear to see that,
similarly to water, the C
2
H
2
emitting column peaks in the inner
disk and then decreases between 0.4 and 1 au. The difference
in the location of the column density drop is due to where the
C
/
O ratio is increased. In the models where C
/
O is increased
within
T
=
500 K, the carbon-rich chemistry is restricted to a
smaller area, whereas in the other models, the C
2
H
2
column is
more spatially extended. It is clear that most models that are
able to match the expectation from the slab model
fi
t have
C
/
O
>
2.
Contrary to CO
2
and H
2
O, in the case of C
2
H
2
, the selection
of the temperature where we transition from solar to a high
C
/
O ratio
(
i.e., 250 K versus 500 K
)
plays an important role in
determining the
fi
nal weighted temperature, as we can see in
Figure
6
, most of the models cluster around a particular value.
In the models where the carbon-rich chemistry is allowed to be
more spatially extended, the C
2
H
2
has a lower temperature.
This implies that a high C
/
O ratio extended over larger radii
would produce an overall lower emitting temperature for the
hydrocarbons. Similarly, by restricting the extent of the high
C
/
O ratio
(
i.e., the 500 K transition models
)
, we limit the
presence of C
2
H
2
to the innermost disk, which in turn results in
a higher emitting temperature since the material is closer to the
star. Comparing to the temperature retrieved from slab models,
we are not able to strictly discriminate between the two
scenarios since most of the
fl
ux-weighted temperatures are
within the uncertainty range. This is also true for water, where
there is an overlap in the
fl
ux-weighted temperatures.
In our approach, the key to distinguishing between a radially
extended or limited carbon-rich chemistry is the emitting area.
Slab models retrieve a maximum emitting area of
()
p
0.25 au
2
for C
2
H
2
, corresponding to the 3
σ
contour shown in Figure
17
.
The 500 K contour for the gas temperature extends to 0.4 au in
the IR-emitting layer
(
Figure
4
)
, whereas it goes past 1 au for
the 250 K contour. This small emitting area, in combination
with the high emitting temperature of C
2
H
2
, indicates that the
carbon chemistry is only released in the innermost disk, where
the sublimation of carbonaceous grains is possible. If the
carbon-rich material present in this system traced by C
2
H
2
is
caused by an advection of material from further out in the disk
(
J. Mah et al.
2023
)
, then it should produce more extended
emission than inferred here.
4.3. Other Hydrocarbons
4.3.1. C
4
H
2
We compare the retrieved C
4
H
2
column to that predicted by
our thermochemical models in Figure
7
. Based on the
χ
2
maps
(
Figure
17
)
from the slab model
fi
tting, this column likely
represents an upper limit. In turn, this makes it consistent with
the models where we assumed C
/
O
=
2. The C
4
H
2
emission is
extended over a larger area than C
2
H
2
and is therefore
compatible with a lower-emitting temperature
(
150 K
)
.To
provide a more de
fi
nite constraint, we explored
fi
tting C
4
H
2
with the same emitting temperature as C
2
H
2
in Appendix
B
and
found that the higher temperature is incompatible with the
Q
-
branch feature. This indicates the presence of a warm
(
<
400 K
)
hydrocarbon-rich reservoir in addition to the hot
(
>
400 K
)
C
2
H
2
. We discuss the potential origin of these two reservoirs in
Section
5.3
.
4.3.2. Nondetections
The chemical network used in this work is able to predict
chemical abundances for over 400 species. Therefore, we
checked the predictions for the abundance of hydrocarbons that
have been detected in hydrocarbon-rich low-mass sources
(
B. Tabone et al.
2023
; A. M. Arabhavi et al.
2024
; J. Kanwar
et al.
2024a
)
, in order to see if we can obtain any additional
constraints on the C
/
O ratio. In the top row of Figure
8
,we
show the predicted column densities for C
2
H
4
,C
2
H
6
, and
C
6
H
6
. In the case of C
2
H
4
and C
2
H
6
, the predicted columns are
lower than
∼
10
14
cm
−
2
for all of the models. Based on this, we
assumed an average column for C
2
H
4
and C
2
H
6
and produced
LTE slab models with two different sets of temperatures and
emitting areas, mimicking the ones found for C
2
H
2
and C
4
H
2
.
Figure 6.
Contribution function-weighted temperatures of carbon and oxygen-
bearing species for the water depletion models. The symbols represent where in
the model the C
/
O ratio is changed, inside
T
=
250 K or
T
=
500 K. The
markers are shifted horizontally for clarity. For comparison, we include the
temperature retrieved from slab models as a black square, with errors
corresponding to the 1
σ
uncertainty.
Figure 7.
Same as Figure
5
, but for C
4
H
2
.
9
The Astrophysical Journal,
977:173
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)
, 2024 December 20
Colmenares et al.
The lower panel of Figure
8
shows the produced spectra, as
well as the parameters assumed for each one. It is clear that the
emission from these molecules would be too faint to be
observable in the DoAr 33 spectrum. This indicates that our
model prediction is consistent with the nondetection of C
2
H
4
and C
2
H
6
. The columns for these two molecules do not have
any discernible trend in terms of the C
/
O ratio, making them
poor C
/
O tracers for this source. Despite this prediction being
consistent with our observations, we note that the predicted
columns for these species are lower than the ones being
detected in low-mass sources
(
A. M. Arabhavi et al.
2024
;
J. Kanwar et al.
2024a
)
. This could be because the formation of
hydrocarbons larger than C
2
H
2
might be sensitive to the
explicit X-ray luminosity and the presence or absence of
cosmic rays
(
E. Raul et al.
2024
)
or due to the completeness of
the hydrocarbon reactions in the chemical network
(
J. Kanwar
et al.
2024b
)
.
In contrast, C
6
H
6
follows a similar trend to C
2
H
2
, where high
column densities are predicted for the high C
/
O ratio models,
as shown in the top right panel of Figure
8
. Because of this, we
attempted a retrieval in the 14.8
–
14.9
μ
m range, where the
main feature is located, using the spectroscopic
fi
les and
partition functions provided by A. M. Arabhavi et al.
(
2024
)
.
We
fi
rst subtracted the contribution from all of the other
detected molecules, adopting the parameters from the best-
fi
t
slab models Table
2
. Then, we estimated the column density of
C
6
H
6
, assuming a given emitting area and temperature. Similar
to the other hydrocarbons, we tested two cases, one where the
C
6
H
6
is cospatial with C
2
H
2
, i.e., a small emitting area and high
temperature, and one where the C
6
H
6
is cospatial with C
4
H
2
,
having a lower temperature and bigger emitting area. The
resulting column density retrieved for each case is overplotted
with the model predictions as horizontal lines in the top right
panel of Figure
8
. The bottom right panel shows the spectra of
both sets of best-
fi
t parameters, overplotted with the observed
spectrum and the composite model of the detected molecules.
Both sets of solutions point toward C
/
O
=
2
–
4, but we are not
able to con
fi
rm the presence of C
6
H
6
in this spectrum.
5. Discussion
We
fi
nd that C
/
O
>
1 is needed to explain the hydrocarbon-
rich environment around DoAr 33. The two methods to
increase the C
/
O ratio are to deplete oxygen and
/
or enrich
carbon. Here, we
fi
rst discuss how C
/
O can be increased
through water sequestration. Then, we argue that C
/
O
>
1
cannot be achieved through oxygen depletion alone and
propose that additional carbon must be supplied to the gas
phase. We explore how much excess carbon is inferred to be
present in the inner disk of DoAr 33 and consider the two main
mechanisms that have been proposed to explain the origin of
this carbon excess. We also discuss the implications of CH
4
detection in the context of carbon grain sublimation.
5.1. Depletion of Water
It has been posited that planetesimals and protoplanets
forming beyond the water iceline could trap a signi
fi
cant
fraction of the oxygen content as long as the ef
fi
ciency of
accretion onto larger bodies is higher than the drift rate of icy
pebbles
(
J. R. Najita et al.
2013
)
. Modeling of dust and gas
dynamics also showed that outer disk gaps, if deep enough, can
reduce or stop the inward
fl
ux of icy pebbles and reduce the
oxygen enrichment of inner disks by reducing water ice
sublimation inside the snowline
(
A. Kalyaan et al.
2021
,
2023
)
.
These scenarios would raise the C
/
O as the inner disk accretes
the remaining oxygen-poor gas. Stellar accretion proceeds over
several million years, encompassing the initial phases of rocky
planet assembly and the main phase of giant planet formation
Figure 8.
The top row shows the column density predictions from the thermochemical models for C
2
H
4
,C
2
H
6
, and C
6
H
6
. The bottom row shows slab models that
simulate the conditions predicted by the thermochemical calculations. The parameters used for each slab model are listed in the
fi
gure. Two sets of slab models were
tested, one cospatial with C
2
H
2
(
orange
)
and one cospatial with C
4
H
2
(
green
)
. These models
(
green and orange
)
are shown on top of the data
(
black
)
in the bottom left.
The pink-shaded region in the bottom right panel corresponds to the same composite model as in Figure
2
.
10
The Astrophysical Journal,
977:173
(
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)
, 2024 December 20
Colmenares et al.
(
L. Hartmann et al.
2016
)
. Thus, if a signi
fi
cant population of
planetesimals forms, this is a possible scenario for raising C
/
O.
However, in this instance, the volatile reservoir in the inner
disk would be mostly dominated by CO and CO
2
gas, meaning
that, at most, the inner disk could reach a C
/
O ratio of
∼
2
/
3
−
1. In the case of DoAr 33, we have shown that
C
/
O
>
1 is needed to reproduce the C
2
H
2
column. Therefore,
even though planetesimal formation in the outer disk could be
invoked to increase C
/
O, an additional release of carbon is
needed to go beyond C
/
O
=
1.
5.2. Total Carbon Content
To understand the source of the carbon enrichment, we
fi
rst
examine the amount of excess carbon that is consistent with the
observations of DoAr 33. In our thermochemical models, we
assume varying degrees of extra carbon being released into the
system initially in the form of CH
4
inside the soot line
(
Table
4
)
. At the midplane in our model the soot line is located
at
∼
0.08 au
(
Figure
4
)
, which results in a maximum of
∼
0.5
×
10
−
3
M
⊕
of carbon released as CH
4
gas for model
water
_
dep
_
co
(
CH
4
=
8.5
×
10
−
5
)
, calculated by integrat-
ing the total CH
4
mass in the disk inside 500 K. Conversely, in
the dust distribution modeling process
(
Appendix
C
)
,we
considered that the amount of refractory organics carried by the
large dust population accounted for 40% of the total dust mass
(
T. Birnstiel et al.
2018
)
. This results in
∼
1.5
×
10
−
3
M
⊕
of
carbon being present as solids inside 0.08 au. Therefore, our
thermochemical models require that, at most, only a third of the
carbon present in refractories is released into the gas.
The presence or absence of carbon grains can strongly
in
fl
uence the carbon content of forming planetary systems
(
E. A. Bergin et al.
2023
)
. In the context of the solar system,
the sublimation of carbon grains has been posited to explain the
carbon depletion found in meteorites and the Earth
(
E. A. Bergin et al.
2015
; J. Li et al.
2021
)
. It is possible that
the carbon grains that are not sublimated to go into forming
planetesimals. However, we stress our models are not self-
consistent. The SED modeling, which includes predetermina-
tion of the dust composition as part of the dust optical
constants, is a separate step from the thermochemical
calculations, each with independent assumptions of the
elemental carbon content in gas and solids.
Thus, it is entirely possible, given the similarity between the
estimate of the excess carbon in the gas and the total carbon
available in the dust
(
within a factor of 3
)
, that all of the solid-
state carbon inside 0.08 au has been released to the gas. We
note that this solution assumes the presence of a dust trap, as
potentially indicated by the Atacama Large Millimeter
/
submillimeter Array
(
ALMA
)
continuum and the SED, and
water depletion to lower the water column. Alternately, as
discussed in Section
4.1
, the overall gas
/
dust ratio may be
lower than assumed by at least an order of magnitude. This
would reduce the water column and allow for solutions with
“
normal or solar
”
water content
(
i.e., the dotted and the solid
lines in Figure
5
)
. In this instance, the C
2
H
2
column would also
be reduced to near the lower end of the allowed range in the
column density. Here, higher C
/
O ratios and carbon content
are required to bring the column closer to the middle of our
retrieved estimate
(
∼
few
×
10
17
cm
−
2
)
. Future work that
combines the effects of carbon destruction on the emission of
both solids and gaseous species is needed to ensure consistency
and derive more accurate estimates. Finally, while carbon
grains represent one potential source term for excess carbon,
other scenarios have been proposed, which are discussed
below.
5.3. Origin of Carbon Enrichment
Currently, there are two potential models for the origin of the
excess carbon. One posits that the carbon supply can originate
in the outer disk via gas accretion of material with C
/
O
>
1
(
J. Mah et al.
2023
)
, and the other suggests that carbon grain
destruction near the soot line can increase the carbon content of
the inner disk
(
J. Li et al.
2021
)
.
We will discuss each in turn but note two things:
fi
rst, in our
analysis, the difference in emitting temperature and area found
for C
2
H
2
and C
4
H
2
suggests that the carbon-rich chemistry in
this source is not necessarily restricted to the innermost disk.
On the same note, ALMA has observed many disks that appear
to have C
/
O
>
1 beyond 10 au
(
e.g., A. D. Bosman et al.
2021b
)
, and temperatures are hot enough to sublimate carbon
grains only in the inner 1 au for T Tauri disks
(
J. Li et al.
2021
)
;
thus, these solutions are likely not exclusive. However, they do
have different implications for the composition of planets.
5.3.1. Carbon-rich Gas Advection
The model presented by J. Mah et al.
(
2023
)
suggests that
the accretion of CH
4
-rich gas into the inner disk can explain the
excess carbon observed in low-mass sources. This scenario
works if pebbles in the outer disk are large enough to be close
to the drift limit, with fragmentation velocities
(
v
frag
)
higher
than 5 m s
−
1
. In this case, the system gets an early in
fl
ux of
water-rich pebbles crossing the water iceline, enhancing the
gas. The in
fl
ux of water-rich pebbles eventually runs out, and
the oxygen-enriched gas gets accreted by the star within
∼
2 Myr. Only then, the system is left with carbon-rich gas that
can be advected into the inner disk.
In this concept, CH
4
is released into the gas with an
abundance that exceeds both CO and CO
2
providing
C
/
O
=
(
CH
4
+
CO
+
CO
2
)
/
(
CO
+
2CO
2
+
H
2
O
)
>
1. This
leads to an important point. In protostellar envelopes, the CO
and CO
2
ice abundances have been determined via Spitzer
spectroscopic surveys and are
∼
60% relative to water
(
K. I. Öberg et al.
2011a
)
. Assuming a water ice abundance
of order
∼
2
×
10
−
4
(
relative to H
2
)(
K. M. Pontoppidan et al.
2004
)
, then the typical abundance of CO and CO
2
ice are of
order
∼
10
−
4
relative to H
2
. This does not account for the gas-
phase CO and CO
2
content, and thus the gas & ices carry
>
25% of the cosmically available carbon, which is 4.28
×
10
−
4
,
relative to H
2
(
M.-F. Nieva & N. Przybilla
2012
)
. In sum, if CO
and CO
2
are present at levels expected in protostellar gas
(
inside their respective ice lines
)
, then to achieve C
/
O
>
1, one
must destroy nearly
all
carbon-rich grains, which hold an
equivalent amount of elemental carbon as the gas
/
ices. This
seems implausible beyond 10 au as the destruction mechanisms
for carbon grains in the outer disk are highly ineffective
(
D. E. Anderson et al.
2017
; L. Klarmann et al.
2018
)
.
However, the ALMA observations of C
/
O
>
1 also coincide
with many systems where the CO gas-phase abundance has
been reduced
(
A. Miotello et al.
2023
)
. Simulations account for
the presence of strong C
2
H emission in these disks via the
release of CH
4
from grains at the level of a few percent of the
solid-state carbon inventory
(
A. D. Bosman et al.
2021a
)
.
These results empirically infer that
(
CH
4
+
CO
+
CO
2
)
/
(
CO
+
11
The Astrophysical Journal,
977:173
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)
, 2024 December 20
Colmenares et al.