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Astron. Astrophys. 361, 1079-1094 (2000) 3. Results3.1. One-point observationsHNCO was detected in 36 SEST sources (from 56 observed) and in 22
OSO sources (from 27). Because of one source belonging to both
samples, the total number of detected objects is 57. In many cases
Table 5 summarizes the 220 GHz SEST results for HNCO
Table 5. C18O (2-1) and HNCO ( Table 6. C18O (1-0) and HNCO ( Examples of measured spectra are given in Fig. 2, Fig. 3.
Fig. 2 shows spectra of a few sources covering
The HNCO line profile in Orion KL can be decomposed into at
least two components which likely correspond to the so-called
classical "Hot Core" and "Plateau" outflow components (see, e.g.,
Harris et al. 1995). The ratio between these components is practically
the same for the An inspection of Table 5 shows that the derived
C18O velocities are systematically lower (more negative)
than the HNCO ones. The difference is
3.2. MapsIn order to estimate source sizes and their spatial association
with YSO and infrared (IR) sources we mapped 2 southern sources in the
The sources remain spatially unresolved. E.g. for
G 301.12-0.20 we obtain a FWHM 3.3. Detection of the
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Fig. 5. Left panel: parts of the Orion low-resolution 220 GHz spectrum corresponding to higher ![]() ![]() ![]() |
There is a weak bump in the redshifted C18O
wing which can be attributed to HNCO
. Due to the uncertainty in fitting
the C18O line profile the intensity of the HNCO feature
cannot be reliably determined but it is lower than reported by Sutton
et al. (1985). Our best estimate for the integrated intensity is
K km/s, but a reliable error
cannot be given.
There is also a feature at the
frequency in the 220 GHz spectrum. It is located in the wing of a
C2H3CN line. The integrated intensity is
K km/s. The identification of
this feature with HNCO seems to be reliable. The only other candidate
is the C2H5OH
line at 219391.81 MHz. However, there is no sign of other ethanol
lines in our spectrum so we reject this alternative. In the
461 GHz spectrum the
feature is
clearly detected. Its integrated intensity is
K km/s.
The HNCO lines are split into several hyperfine components mainly
due to the 14N spin. This splitting is clearly seen in the
transition (Fig. 3) at
22 GHz. Earlier HNCO hyperfine structure in the
line was only observed in the dark
cloud TMC-1 (Brown 1981) where possible deviations from the optically
thin LTE (Local Thermodynamic Equilibrium) intensity ratios (3:5:1)
were found. In our spectra the hyperfine ratios are consistent with
the optically thin LTE values. Taking into account the measurement
uncertainties, an upper limit on the optical depth in this transition
for the sources detected in Effelsberg is
.
To the best of our knowledge no isotopomer of HNCO except the main
one has been detected in space yet. This detection would be important
for estimates of HNCO optical depths which are believed to be small
(e.g. Jackson et al. 1984; Churchwell et al. 1986). The frequency
separations between the HN13CO and the main isotopomer
lines are rather small corresponding to a few km/s, so in sources with
broad lines like Orion A or Sgr A the HN13CO
lines will be blended. However, there are some strong HNCO sources in
our sample with narrower lines which show features attributable to
HN13CO. The most reliable one is seen in the
G 301.12-0.20 spectrum
(Fig. 6). A weak feature on the blue shoulder of the main isotope
line is very close in frequency to the expected location of the
HN13CO line.
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Fig. 6. The HNCO ![]() ![]() |
For comparison we show in addition to HNCO also the C34S spectrum. It is noteworthy that there is no bump in this spectrum corresponding to the discussed feature in HNCO.
The line we identify with HN13CO is shifted by
MHz from the expected
HN13CO transition frequency. This
shift, if it is significant, cannot
be explained by instrumental effects like in the case of our
C18O data because the feature is very close to the main
isotope line. The shift greatly exceeds the uncertainty of the
transition frequency derived from the laboratory data (Winnewisser et
al. 1976) which is 25 kHz. This makes the identification
questionable. Detection of other HN13CO lines would be
important in this respect. There is no corresponding feature in the
HNCO spectrum (the
spectrum is too noisy). This could
mean that the optical depth in this transition is significantly lower.
Indeed, at sufficiently high temperatures
(
K) it can be about 2 times
lower than in the
transition
according to Eq. (2) (see the discussion in Sect. 4.2).
If our identification of the discussed line with HN13CO
is correct we can estimate the optical depth assuming the same
excitation as for the main isotopomer. For G 301.12-0.20 we
obtain if we assume the terrestrial
12C/13C isotope ratio
(12C/13C = 89) and
for 12C/13C =
40. A high optical depth in the
HNCO
line does not contradict our conclusion of low optical depth in the
transition because the line strengths
for these transitions are different (see discussion in
Sect. 4.2). Therefore, the optical depth in some lines of
the main isotopomer might be rather high. This contradicts the usual
assumption of low optical depth in all HNCO lines (e.g., Jackson et
al. 1984; Churchwell et al. 1986) and could imply serious consequences
for the analysis of HNCO excitation and abundances.
© European Southern Observatory (ESO) 2000
Online publication: October 10, 2000
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