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Table 3

Spectral-line results for ammonia, hydrogen sulphide, hydroxyl, and silicon monoxide.

Species and Rotational Eupp/k Rest freq. Setting & rms Peak Area Veloc. range
elec./vibr. state quantum nums. (K) (GHz) sideband (mK) (mK) (K km s-1) LSR (km s-1) Comments

ortho-NH3v = 0 JK = 27 572.498 14 USB 6.6 (1.05) 308 15.5 [–50; +65]
JK = 170 1763.525 19 LSB 77.8 (1.02) 1441 68.9 g-fitted
para-NH3v = 0 JK = 127 1763.821 19 LSB 77.8 (1.02) 450 21.0 g-fitted
JK = 143 1763.602 19 LSB 77.8 (1.02) ≲100 ≲4.5
ortho-H2S v = 0 JKa,Kc = 31,2–22,1 117 1196.012 05 LSB 88.8 (1.01) 177 10.3 g-fitted
para-H2S v = 0 JKa,Kc = 31,3–20,2 103 1002.779 09 USB 33.1 (1.05) 97 4.22 g-fitted tent. detec.
JKa,Kc = 52,4–51,3 303 1862.436 01 LSB 90.9 (0.97) 590 11.8 g-fitted
OH v = 0 J = 3/2–1/2 270 1834.747 16 LSB 55.5 (0.98) 1768 85.5 [–40; +90]
28SiO v = 0 J = 14–13 219 607.608 13 LSB 5.4 (0.99) 370 15.5 [–40; +105]
J = 16–15 283 694.294 17 USB 13.4 (1.08) 384 15.1 [–35; +85]
v = 1 J = 13–12 1957 560.325 14 LSB 6.6 (1.08) 76 2.13 [–15; +67]
J = 15–14 2017 646.429 12 LSB 7.8 (0.93) 108 3.01 [–20; +60]
J = 23–22 2340 990.355 09 LSB 33.1 (1.06) 178 5.12 g-fitted
J = 27–26 2550 1161.945 06 USB 59.5 (1.03) 190 5.36 g-fitted
J = 40–39 3462 1717.236 04 USB 64.5 (1.05) 160 4.98 g-fitted tent. detec.
v = 2 J = 26–25 4282 1111.235 07 USB 22.0 (1.08) 140 3.43 g-fitted
J = 27–26 4297 1153.804 06 LSB 59.5 (1.04) 925 25.3 g-fitted maser ?
J = 28–27 4355 1196.353 05 LSB 88.8 (1.01) 50 2.50 g-fitted tent. detec.
29SiO v = 0 J = 13–12 187 557.179 14 LSB 6.6 (1.08) 138 5.73 [–15; +75]
J = 26–25 722 1112.798 07 USB 22.0 (1.08) 203 7.07 g-fitted
v = 1 J = 16–15 2036 680.865 17 LSB 13.4 (1.10) 35 0.97 g-fitted
30SiO v = 0 J = 26–25 713 1099.708 07 LSB 22.0 (1.09) 231 6.47 [–20; +70]
J = 42–41 1832 1771.251 19 USB 77.8 (1.02) 153 3.68 g-fitted tent. detec.

Notes.

(†)

Since ortho- and para-NH3 behave as different chemical species, for para-NH3 the level excitation energies are relative to that of the lowest para level (JK = ), while for ortho-NH3 are given w.r.t. the JK = level. Since the ortho and para spin isomer variants of hydrogen sulphide behave as different chemical species, for ortho-H2S the level excitation energy is relative to its lowest (ortho) energy level, the JKa,Kc = 10,1, while for the para species they are given w.r.t. the JKa,Kc = 00,0 ground level.

(‡)

For the spectral resolution in km s-1 given in parentheses.

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