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Table A.4

Triple-Gaussian fitting results for CO, H2O, NH3, SiO, SO, and SO2.

Central component HEVW components
Species and Rotational E upp Peak FWHM Blue peak FWHM Red Peak
elec./vibr. state quantum nums. (K) Tmb (mK) (km s-1) Tmb (mK) (km s-1) Tmb (mK)

12CO v = 0 J = 6–5 116 1091 38 292 19 366
J = 10–9 304 1499 37 366 22 452
J = 16–15 752 1296 31 205 17 264
13CO v = 0 J = 6–5 111 82 49 48 12 38
J = 9–8 238 131 47
J = 10–9 291 173 39
J = 16–15 719 257 19
ortho-H2O v = 0 JKa,Kc = 11,0–10,1 27 1143 43 −253 17 92
JKa,Kc = 30,3–21,2 163 4664 43 −1514 17 538
JKa,Kc = 31,2–30,3 215 1809 45 −268 21 232
JKa,Kc = 31,2–22,1 215 2919 46 −425 13 310
JKa,Kc = 32,1–31,2 271 2009 41 −25 25 364
JKa,Kc = 53,2–52,3 698 1802 31
v2 = 1 JKa,Kc = 21,2–10,1 2379 1007 32
JKa,Kc = 82,7–83,4 3556 46 16
para-H2O v = 0 JKa,Kc = 11,1–00,0 53 3140 43 −804 18 373
JKa,Kc = 20,2–11,1 101 3317 40 −469 12 287
JKa,Kc = 21,1–20,2 137 1570 45 −101 23 267
JKa,Kc = 42,2–41,3 454 1183 50 16 167
JKa,Kc = 63,3–62,4 952 1011 31
v2 = 1 JKa,Kc = 11,1–00,0 2352 244 28
v2 = 2 JKa,Kc = 21,1–20,2 4684 114 27
v3 = 1 JKa,Kc = 63,3–62,4 6342 169 27
ortho-HO v = 0 JKa,Kc = 31,2–30,3 215 209 34
para-HO v = 0 JKa,Kc = 11,1–00,0 53 205 35 −62 19 47
ortho-HO v = 0 JKa,Kc = 30,3–21,2 162 350 26
JKa,Kc = 31,2–30,3 215 232 35
para-HO v = 0 JKa,Kc = 11,1–00,0 53 126 38 −49 11 −9
JKa,Kc = 20,2–11,1 101 72 35
ortho-NH3v = 0 JK= 27 235 41 89 19 183
JK= 170 1441 45
para-NH3v = 0 JK= 127 450 44
OH v = 0 J = 3/2–1/2 270 1695 40 122 19 641
28SiO v = 0 J = 14–13 219 369 32 41 25 65
J = 16–15 283 378 28 43 23 90
29SiO v = 0 J = 13–12 187 118 41 12 25 20
J = 26–25 722 203 32
30SiO v = 0 J = 26–25 713 193 23
J = 42–41 1832 153 22
SO v = 0 JN = 1314–1213 193 70 32 2 24 26
JN = 1312–1211 194 60 31 0 24 20
JN = 1313–1212 201 64 29 10 21 30
JN = 1516–1415 253 75 35 5 13 10
SO2v = 0 JKa,Kc = 165,11–154,12 186 16 29 −4 14 19

Notes.

(†)

Since the ortho and para spin isomer variants of both water and ammonia behave as different chemical species, for all ortho transition Eupp/k values are relative to the corresponding lowest ortho energy level, while for the para transitions they are given w.r.t. the corresponding lowest para energy level.

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