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Table A.1

Parameters and fitting results for lines detected toward FG0.89SW.

Rest Freq. Transition Sul El/kB V0 ΔV τdV
(MHz) (K) (km s-1) (km s-1) (10-3 km s-1)

87284.105 C2N = 1–0 J = 3/2–1/2 F = 1–1 0.04 0.0 –0.45( 0.03) 20.90( 0.10) 777.( 0.)
87316.898 C2N = 1–0 J = 3/2–1/2 F = 2–1 0.42 0.0 7625.( 21.)
87328.585 C2N = 1–0 J = 3/2–1/2 F = 1–0 0.21 0.0 3799.( 0.)
87401.989 C2N = 1–0 J = 1/2–1/2 F = 1–1 0.21 0.0 3805.( 0.)
87407.165 C2N = 1–0 J = 1/2–1/2 F = 0–1 0.08 0.0 1528.( 0.)
87446.470 C2N = 1–0 J = 1/2–1/2 F = 1–0 0.04 0.0 780.( 0.)
88631.602 HCN  J = 1–0 1.00 0.0 –2.83( 0.01) 28.90( 0.01) 68 695.( 113.)
86339.922 H13CN  J = 1–0 1.00 0.0 –2.27( 0.14) 21.40( 0.30) 1821.( 25.)
86054.966 HC15J = 1–0 1.00 0.0 342.( 19.)
90663.568 HNC  J = 1–0 1.00 0.0 –1.75( 0.02) 20.80( 0.10) 24 767.( 68.)
87090.825 HN13J = 1–0 1.00 0.0 498.( 18.)
88865.715 H15NC  J = 1–0 1.00 0.0 70.( 18.)
93173.392 N2H+  J = 1–0 1.00 0.0 –3.29( 0.12) 21.00( 0.30) 7341.( 84.)
89188.525 HCO+  J = 1–0 1.00 0.0 –2.43( 0.02) 32.40( 0.01) 67 923.( 102.)
86754.288 H13CO+  J = 1–0 1.00 0.0 –1.83( 0.07) 18.40( 0.20) 3079.( 25.)
85162.223 HC18O+  J = 1–0 1.00 0.0 1310.( 28.)
87057.535 HC17O+  J = 1–0 1.00 0.0 69.( 17.)
89487.414 HOC+  J = 1–0 1.00 0.0 –0.78( 0.39) 20.50( 0.90) 626.( 24.)
86670.760 HCO  NK = 101–000J = 3/2–1/2 F = 2–1 0.42 0.0 1.44( 0.59) 18.10( 1.40) 309.( 22.)
86708.360 HCO  NK = 101–000J = 3/2–1/2 F = 1–0 0.25 0.0 115.( 19.)
86777.460 HCO  NK = 101–000J = 1/2–1/2 F = 1–1 0.25 0.0 118.( 20.)
86805.780 HCO  NK = 101–000J = 1/2–1/2 F = 0–1 0.08 0.0 47.( 19.)
63992.975 CH2NH  101–000 2.25 0.0 –0.71( 0.36) 13.80( 0.80) 301.( 16.)
72837.948 H2CO(p)  JKa,Kc = 101–000 1.00 0.0 –1.00( 0.04) 20.30( 0.10) 6061.( 22.)
78135.183 CH3NH2(o)  213–202 30.00 6.7 –6.19( 1.64) 20.60( 3.90) 60.( 21.)
79008.422 CH3NH2(o)  112–103 18.00 2.4 84.( 21.)
89956.068 CH3NH2(p)  110–101 6.00 2.1 110.( 25.)
60531.489 CH3OH  101–2-12 E 1.80 12.5 –5.26( 0.51) 21.20( 1.20) 431.( 21.)
76198.726 l-C3J = 7/2–5/2 3.85 4.2 0.18( 0.50) 17.50( 1.00) 222.( 8.)
76199.928 l-C3J = 7/2–5/2 2.85 4.2 167.( 0.)
76204.182 l-C3J = 7/2–5/2 3.85 4.2 222.( 0.)
76205.103 l-C3J = 7/2–5/2 2.85 4.2 167.( 0.)
82966.200 c-C3H2(o)  312–303 2.93 12.1 –0.94( 0.07) 18.70( 0.20) 439.( 27.)
85338.893 c-C3H2(o)  212–101 4.50 2.3 4013.( 34.)
59557.896 c-C3H2(p)  331–322 1.37 16.1 71.( 15.)
82093.559 c-C3H2(p)  202–111 1.37 2.5 1211.( 20.)
61797.009 l-C3H2(o)  313–212 8.00 16.3 –1.93( 0.00) 21.10( 2.60) 72.( 17.)
62950.993 l-C3H2(o)  312–211 8.00 16.4 132.( 18.)
82395.089 l-C3H2(o)  414–313 11.25 19.3 117.( 21.)
83165.345 l-C3H2(p)  303–202 4.00 6.0 83.( 23.)
60366.000 H2CCN(o)  303–202 54.00 2.9 –1.83( 2.03) 17.90( 4.50) 264.( 47.)
80486.000 H2CCN(o)  404–303 72.00 5.8 191.( 30.)
85457.300 CH3CCH  JK = 40–30 10.00 8.2 0.59( 1.54) 15.60( 4.00) 130.( 44.)
73577.451 CH3CN  JK = 43–33 7.00 69.6 –2.70( 0.00) 21.60( 0.00)
73584.543 CH3CN  JK = 42–32 6.00 33.9
73588.799 CH3CN  JK = 41–31 7.50 12.4
73590.218 CH3CN  JK = 40–30 8.00 5.3
91958.726 CH3CN  JK = 54–44 3.60 123.1
91971.130 CH3CN  JK = 53–43 12.80 73.1
91979.994 CH3CN  JK = 52–42 8.40 37.4
91985.314 CH3CN  JK = 51–41 9.60 16.0
91987.088 CH3CN  JK = 50–40 10.00 8.8
60058.127 H2CCO(o)  313–212 8.00 15.9 –1.62( 0.99) 21.20( 2.30) 132.( 18.)
61190.279 H2CCO(o)  312–211 8.00 16.0 130.( 18.)
80076.652 H2CCO(o)  414–313 11.25 18.8 76.( 19.)
81586.230 H2CCO(o)  413–312 11.25 18.9 90.( 20.)
65944.301 HNCO  303–202 3.00 3.2 –5.12( 0.88) 22.00( 2.10) 72.( 17.)
87925.237 HNCO  404–303 4.00 6.3 247.( 21.)
86846.960 SiO  J = 1–0 2.00 2.1 –2.29( 0.18) 20.60( 0.40) 1262.( 22.)
85759.199 29SiO  J = 1–0 2.00 2.1 112.( 28.)
57722.670 CH3CHO  303–202 A 3.25 2.8 –0.80( 0.73) 19.30( 1.70) 99.( 25.)
59285.370 CH3CHO  312–211 E 2.85 5.2 90.( 16.)
59379.499 CH3CHO  312–211 A 2.88 5.1 81.( 16.)
74891.677 CH3CHO  414–313 A 4.00 7.7 94.( 17.)
74924.134 CH3CHO  414–313 E 4.00 7.7 122.( 17.)
76866.436 CH3CHO  404–303 E 4.32 5.6 87.( 21.)
76878.953 CH3CHO  404–303 A 4.32 5.5 85.( 20.)
79099.313 CH3CHO  413–312 E 4.00 8.1 74.( 20.)
79150.166 CH3CHO  413–312 A 4.00 8.0 89.( 20.)
69002.890 NS  J = 3/2–1/2 F = 5/2–3/2e 2.00 1.1 –2.61( 0.78) 20.90( 1.80) 129.( 12.)
69017.991 NS  J = 3/2–1/2 F = 3/2–1/2e 0.74 1.1 48.( 0.)
69037.497 NS  J = 3/2–1/2 F = 3/2–3/2e 0.59 1.1 38.( 0.)
69040.324 NS  J = 3/2–1/2 F = 1/2–1/2e 0.59 1.1 38.( 0.)
69059.844 NS  J = 3/2–1/2 F = 1/2–3/2e 0.07 1.1 5.( 0.)
69283.195 NS  J = 3/2–1/2 F = 1/2–3/2f 0.07 1.1 5.( 0.)
69330.592 NS  J = 3/2–1/2 F = 3/2–3/2f 0.59 1.1 49.( 0.)
69411.943 NS  J = 3/2–1/2 F = 5/2–3/2f 2.00 1.1 135.( 14.)
69437.850 NS  J = 3/2–1/2 F = 1/2–1/2f 0.59 1.1 40.( 0.)
69485.223 NS  J = 3/2–1/2 F = 3/2–1/2f 0.74 1.1 50.( 0.)
69746.747 H2CS(o)  211–110 4.50 14.8 –1.60( 0.79) 14.10( 1.90) 90.( 13.)
68699.385 H2CS(p)  202–101 2.00 1.6 67.( 11.)
62931.800 SO  JK = 21–10 1.92 1.4 –1.01( 0.30) 19.70( 0.70) 644.( 20.)
86093.950 SO  JK = 22–11 1.50 15.2 53.( 18.)
69408.371 SO+  J = 3/2–1/2 e 1.31 0.0 1.54( 2.00) 20.00( 0.00) 63.( 10.)
69783.846 SO+  J = 3/2–1/2 f 1.31 0.0 63.( 0.)
57083.814 C4N = 6–5 J = 13/2–11/2 13.00 6.8 –1.05( 0.59) 18.50( 1.40) 165.( 28.)
57122.461 C4N = 6–5 J = 11/2–9/2 11.00 6.9 79.( 26.)
66600.700 C4N = 7–6 J = 15/2–13/2 15.00 9.6 114.( 16.)
66639.313 C4N = 7–6 J = 13/2–11/2 13.00 9.6 143.( 16.)
76117.438 C4N = 8–7 J = 17/2–15/2 17.00 12.8 177.( 20.)
76156.031 C4N = 8–7 J = 15/2–13/2 15.00 12.8 150.( 20.)
85634.012 C4N = 9–8 J = 19/2–17/2 19.00 16.4 89.( 27.)
85672.578 C4N = 9–8 J = 17/2–15/2 17.00 16.5 66.( 26.)
63686.052 HC3J = 7–6 7.00 9.2 –3.90( 0.46) 21.40( 0.90) 396.( 20.)
72783.822 HC3J = 8–7 8.00 12.2 300.( 17.)
81881.468 HC3J = 9–8 9.00 15.7 236.( 20.)
90979.023 HC3J = 10–9 10.00 19.6 151.( 28.)
57229.067 C2JN = 54–43 5.00 5.4 –1.35( 0.83) 18.20( 2.00) 84.( 27.)
69281.115 C2JN = 65–54 6.00 8.2 142.( 14.)
81505.170 C2JN = 76–65 7.00 11.5 72.( 18.)

Notes. For species with hyperfine structure, the relative intensities were fixed, and the given uncertainty corresponds to that in the total integrated intensity.

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