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Table 5:

Integrated optical depths of optically thin lines (see Sects. 4.1.2 and 4.1.3) and resulting excitation temperatures.
Species $\int{\tau {\rm d}V}$ Excitation temperature
  $J =1 \leftarrow0$ $J=2\leftarrow1^a$ $J=2\leftarrow1/J=1\leftarrow0^a$ $T_{\rm ex, 1-0}^b$ $T_{\rm ex, 2-1}^{a,b}$ $T_{\rm ex,LTE}^c$
  (km s-1)   (K)
SiO $0.412\pm0.021$ $1.440\pm0.270$ $3.495\pm0.679$ 5.51 5.21 23
C34Sa $0.292\pm0.020$ $0.440\pm0.040$ $1.507\pm0.172$ 5.83 5.27 $7.2\pm0.4$
H13CO+ $2.804\pm0.259$ $2.500\pm0.050$ $0.892\pm0.084$ 5.20 5.17 $3.8\pm0.3$
H13CN $1.791\pm0.243$ $2.100\pm0.080$ $1.173\pm0.165$ 5.37 5.24 $4.8\pm0.5$
HN13C $0.307\pm0.181$ $0.900\pm0.070$ $2.932\pm1.743$ 5.20 5.17 -
CS-NEd $0.080\pm0.010$ $0.280\pm0.080$ $3.500\pm1.092$ - - $11 \pm 3 $
a In the cases of C34S and CS, $J=2 \leftarrow1$ should be replaced by $J =4 \leftarrow3$. With the exception of the SiO $J=2 \leftarrow1$ line (Fig. 3), the $J=2 \leftarrow1$ and $4\leftarrow3$ data were taken from Muller et al. (2006). b LVG excitation temperatures of optically thin lines with $T_{\rm kin} = 80$ K, $T_{\rm CMB} = 5.14$ K, and n(H 2) = 2000 cm-3. c Excitation temperatures under conditions of Local Thermodynamical Equilibrium (LTE). For the uncertainty in the estimate from SiO (this includes so far unpublished SiO J=4-3 data), see Sect. 4.1.2. d CS absorption toward the north-eastern continuum component, displaced from the main absorption line by -147 km s-1. Since no spatial density has been derived for this feature, Cols. 5 and 6 are left empty.

Source LaTeX | All tables | In the text

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