Open Access
Table A.2
Measured parameters of identified molecular transitions in the three cores.
Transitions | 869 | 1390 | 4149 | ||||||
---|---|---|---|---|---|---|---|---|---|
W | FWHM | VLSR | W | FWHM | VLSR | W | FWHM | VLSR | |
(mK km s−1) | (km s−1) | (km s−1) | (mK km s−1) | (km s−1) | (km s−1) | (mK km s−1) | (km s−1) | (km s−1) | |
c-C3HD 32,2 – 31,3 | ≤4.0 | 4.5(1.2) | 0.35(0.10) | 11.2 | ≤3.6 | ||||
c-C3HD 21,2 – 10,1 | ≤4.0 | 86.9(8.8) | 0.62(0.01) | 11.2 | 193(19.3) | 0.51(0.01) | -2.0 | ||
c-C3HD 21,1 – 11,0 | ≤4.9 | 19.7(2.6) | 0.58(0.05) | 11.2 | 39.3(4.2) | 0.42(0.03) | -2.0 | ||
c-CC13CH2 20,2 – 11,1 | ≤4.0 | ≤4.4 | 17.9(2.1) | 0.37(0.03) | -2.1 | ||||
c-CC13CH2 21,2 – 10,1 | ≤4.0 | ≤4.4 | 18.1(2.2) | 0.39(0.03) | -1.8 | ||||
c-CC13CH2 31,2 – 30,3 | ≤3.9 | ≤4.3 | 5.8(1.4) | 0.48(0.14) | -2.0 | ||||
H2CCO 41,4 – 31,3 | 23.6(2.7) | 0.61(0.05) | -5.0 | 23.1(2.7) | 0.75(0.06) | 11.4 | 19.1(2.2) | 0.47(0.04) | -2.0 |
H2CCO 40,4 – 30,3 | 15.8(2.0) | 0.58(0.07) | -5.0 | 12.7(1.9) | 0.87(0.15) | 11.4 | 13.0(1.8) | 0.46(0.06) | -1.9 |
H2CCO 41,3 – 31,2 | 19.4(2.4) | 0.63(0.06) | -5.0 | 11.2(1.8) | 0.89(0.13) | 11.4 | 15.3(1.9) | 0.41(0.03) | -2.0 |
H2CCO 51,5 – 41,4 | 18.0(2.3) | 0.47(0.04) | -5.0 | 14.1(2.3) | 0.7(0.3) | 11.4 | 13.0(1.9) | 0.38(0.04) | -1.9 |
H2CCO 50,5 – 40,4 | 11.7(2.0) | 0.53(0.07) | -4.9 | ≤5.3 | 10.2(1.7) | 0.41(0.05) | -1.9 | ||
C3S 14 – 13 | ≤ 1.6 | ≤4.0 | 10.3(1.6) | 0.41(0.05) | -1.9 | ||||
CH2DCCH 51,5 – 41,4 | ≤4.0 | ≤4.4 | 6.7(1.2) | 0.32(0.07) | -1.9 | ||||
CH2DCCH 50,5 – 40,4 | ≤4.0 | ≤4.4 | 11.9(1.6) | 0.44(0.06) | -1.9 | ||||
CH2DCCH 51,4 – 41,3 | ≤4.0 | ≤4.4 | 7.7(1.4) | 0.43(0.07) | -1.9 | ||||
CH2DCCH 61,6 – 51,5 | ≤4.9 | ≤5.4 | 7.2(1.6) | 0.40(0.04) | -2.0 | ||||
CH2DCCH 60,6 – 50,5 | ≤4.9 | ≤5.4 | 12.8(1.9) | 0.34(0.03) | -2.0 | ||||
CH2DCCH 61,5 – 51,4 | ≤4.9 | ≤5.4 | 8.9(1.5) | 0.32(0.04) | -2.0 | ||||
HNO 10,1 – 00,0 | 57.8(5.9) | 0.67(0.02) | -5.3 | 12.1(1.8) | 0.62(0.07) | 11.1 | 7.3(1.4) | 0.46(0.08) | -2.2 |
CCS NJ=67 – 56 | 11.7(1.7) | 0.49(0.02) | -5.1 | 72.4(7.3) | 0.57(0.01) | 11.1 | 157.1(15.8) | 0.45(0.01) | -2.1 |
CCS NJ=87 – 76 | ≤4.8 | 13.5(1.9) | 0.39(0.05) | 11.3 | 15.7(2.0) | 0.29(0.03) | -1.8 | ||
HC3N 9 – 8 | ≤4.0 | 273.6(27.4) | 0.58(0.01) | 11.3 | 265.8(26.7) | 0.42(0.01) | -1.9 | ||
HC3N 11 –10 | ≤4.8 | 88.9(9.0) | 0.57(0.01) | 11.3 | 88.6(8.9) | 0.36(0.01) | -1.9 | ||
p-c-C3H2 20,2 – 11,1 | 17.9(2.2) | 0.61(0.05) | -5.0 | 168.1(16.9) | 0.59(0.01) | 11.3 | 151.7(15.2) | 0.47(0.01) | -1.9 |
p-c-C3H2 32,2 – 31,3 | ≤3.9 | 20.4(2.5) | 0.53(0.05) | 11.3 | 11.5(1.6) | 0.31(0.04) | -1.9 | ||
l-C3H2 41,4 – 31,3 | ≤4.0 | 18.6(2.3) | 0.69(0.07) | 11.2 | 10.9(11.3) | 0.51(0.05) | -2.0 | ||
l-C3H2 40,4 – 30,3 | ≤4.0 | 8.9(1.6) | 0.51(0.08) | 11.4 | 7.7(1.3) | 0.62(0.08) | -2.1 | ||
l-C3H2 41,3 – 31,2 | ≤3.9 | 19.2(2.3) | 0.53(0.04) | 11.3 | 11.1(1.6) | 0.38(0.05) | -1.8 | ||
o-c-C3H2 31,2 – 30,3 | ≤3.9 | 67.1(6.8) | 0.52(0.02) | 11.2 | 28.1(3.1) | 0.41(0.02) | -2.0 | ||
o-c-C3H2 21,2 – 10,1 | 62.7(6.4) | 0.66(0.02) | -4.9 | 366.8(36.7) | 0.61(0.01) | 11.3 | 302(30.4) | 0.42(0.01) | -1.9 |
CH3O N = 1 − 0, K = 0, J = 3∕2 − 1∕2, F = 1 − 1, Λ = −1 | 5.9(1.5) | 0.46(0.04) | -4.9 | ≤4.3 | ≤3.5 | ||||
CH3O N = 1 − 0, K = 0, J = 3∕2 − 1∕2, F = 2 − 1, Λ = −1 | 7.6(1.5) | 0.49(0.05) | -4.9 | ≤4.3 | 4.8(1.3) | 0.47(0.11) | -1.9 | ||
CH3O N = 1 − 0, K = 0, J = 3∕2 − 1∕2, F = 2 − 1, Λ = +1 | 9.9(1.6) | 0.63(0.10) | -4.9 | 7.7(1.6) | 0.46(0.10) | 11.4 | ≤3.5 | ||
HOCN 40,4 – 30,3 | ≤3.9 | ≤4.3 | 8.5(1.4) | 0.52(0.07) | -1.9 | ||||
DC3N 10 – 9 | ≤3.9 | 19.1(2.3) | 0.62(0.05) | 11.2 | 14.5(1.8) | 0.41(0.03) | -1.9 | ||
OCS 7 – 6 | 38.1(4.0) | 0.57(0.03) | -4.9 | 29.5(3.4) | 0.84(0.06) | 11.2 | 24.2(2.7) | 0.38(0.02) | -1.9 |
OCS 8 – 7 | 34.4(3.8) | 0.53(0.03) | -4.9 | 24.1(3.1) | 0.80(0.08) | 11.3 | 18.7(2.3) | 0.37(0.02) | -1.9 |
o-D2CS | ≤3.9 | 18.9(2.3) | 0.39(0.05) | 11.3 | 23.1(2.5) | 0.36(0.02) | -1.9 | ||
HC18O+ 1 – 0 | 8.8(1.5) | 0.49(0.08) | -4.9 | 37.7(4.0) | 0.59(0.03) | 11.2 | 28.5(3.0) | 0.36(0.02) | -2.0 |
HCS+ 2 – 1 | 21.7(2.5) | 0.52(0.04) | -4.8 | 18.5(2.3) | 0.68(0.06) | 11.5 | 40.0(4.2) | 0.42(0.01) | -1.8 |
e-CH3CCH 52 – 42 | ≤3.9 | ≤4.3 | 4.7(1.2) | 0.43(0.11) | -2.0 | ||||
e-CH3CCH 51 – 41 | ≤3.9 | 18.6(2.5) | 0.92(0.09) | 11.4 | 40.0(4.1) | 0.43(0.01) | -1.9 | ||
e-CH3CCH 50 – 40 | ≤3.9 | 13.4(1.9) | 0.78(0.10) | 11.3 | 42.1(4.4) | 0.42(0.01) | -1.9 | ||
HOCO+ 40,4 – 30,3 | ≤3.9 | 10.2(1.7) | 0.45(0.08) | 11.3 | 10.2(1.5) | 0.42(0.05) | -1.9 | ||
C4H N = 9–8 J = 9.5–8.5 | 9.6(2.0) | 0.95(0.19) | -5.0 | 58.8(6.0) | 0.58(0.02) | 11.4 | 48.6(5.0) | 0.35(0.01) | -1.9 |
C4H N = 9–8 J = 8.5–7.5 | 4.3(1.2) | 0.43(0.13) | -5.0 | 53.5(5.7) | 0.58(0.02) | 11.3 | 49.5(5.1) | 0.30(0.01) | -1.9 |
C4H N = 10–0 J= 10.5–9.5 | ≤4.9 | 49.8(5.2) | 0.63(0.02) | 11.4 | 23.9(2.7) | 0.36(0.02) | -1.9 | ||
C4H N = 10–0 J= 9.5–8.5 | ≤4.9 | 47.8(5.1) | 0.66(0.02) | 11.4 | 22.1(2.6) | 0.37(0.02) | -1.9 | ||
NH2D 11,1 – 10,1 F = 0–1 | ≤3.9 | 111.1(11.2) | 0.52(0.01) | 11.3 | 49.8(5.1) | 0.48(0.01) | -1.8 | ||
NH2D 11,1 – 10,1 F = 2–1 | ≤3.9 | 141.2(14.2) | 0.55(0.01) | 11.2 | 70.7(7.2) | 0.47(0.01) | -1.9 | ||
NH2D 11,1 – 10,1 F = 2–2 | ≤3.9 | 145.3(14.6) | 0.54(0.01) | 11.3 | 159.8(16.0) | 0.59(0.01) | -1.9 | ||
NH2D 11,1 – 10,1 F = 1–2 | ≤3.9 | 139.4(14.1) | 0.54(0.01) | 11.3 | 58.8(6.0) | 0.50(0.01) | -1.8 | ||
NH2D 11,1 – 10,1 F = 1–0 | ≤3.9 | 133.6(13.9) | 0.65(0.01) | 11.3 | 58.1(5.9) | 0.46(0.01) | -1.9 | ||
E-CH3CHO 50,5 – 40,4 | 5.8(1.6) | 0.45(0.11) | -4.9 | 14.5(2.0) | 0.40(0.05) | 11.4 | 10.6(1.8) | 0.43(0.04) | -2.0 |
E-CH3CHO 31,3 – 20,2 | ≤4.8 | ≤5.2 | 5.1(1.4) | 0.34(0.08) | -2.0 | ||||
A-CH3CHO 50,5 – 40,4 | 5.7(1.4) | 0.31(0.06) | -4.9 | ≤5.3 | 12.3(1.8) | 0.38(0.04) | -1.9 | ||
A-CH3CHO 51,4 – 41,3 | ≤4.8 | 11.3(1.1) | 0.42(0.11) | 11.3 | 5.9(1.3) | 0.27(0.08) | -2.0 | ||
C3O 10 – 9 | ≤3.9 | ≤4.9 | 5.7(1.4) | 0.31(0.07) | -1.9 | ||||
C34S 2 – 1 | 97.8(9.9) | 0.59(0.01) | -5.0 | 114.4(11.5) | 0.64(0.01) | 11.3 | 89.5(9.0) | 0.38(0.01) | -2.0 |
E-CH3OH 5−1 – 40 | ≤3.9 | 7.0(1.9) | 0.93(0.19) | 11.6 | 5.6(1.3) | 0.32(0.09) | -1.9 | ||
E-CH3OH 2−1 – 1−1 | 308.1(30.8) | 0.46(0.01) | -5.0 | 381.5(38.2) | 0.56(0.01) | 11.2 | 325.5(32.5) | 0.34(0.01) | -1.9 |
E-CH3OH 20 – 10 | 27.5(3.1) | 0.49(0.03) | -4.9 | 26.8(3.2) | 0.60(0.04) | 11.3 | 38.3(4.1) | 0.35(0.01) | -1.9 |
A-CH3OH 20 – 10 | 402.4(40.3) | 0.46(0.01) | -5.0 | 283.7(28.4) | 0.57(0.01) | 11.3 | 423.0(42.3) | 0.35(0.01) | -1.9 |
A-CH3OH 21 – 11 | ≤4.9 | ≤5.4 | 5.0(1.3) | 0.30(0.09) | -1.9 | ||||
34SO 23 – 12 | 86.7(8.7) | 0.51(0.01) | -5.2 | 114.4(11.5) | 0.56(0.01) | 11.1 | 46.9(4.9) | 0.42(0.01) | -2.2 |
c-C3D2 31,3 – 20,2 | ≤4.9 | 8.9(1.6) | 0.39(0.08) | 11.2 | 8.5(1.7) | 0.45(0.05) | -1.9 | ||
CS 2 – 1 | 307.5(30.8) | 0.94(0.01) | -4.8 | 794.8(79.5) | 0.78(0.01) | 11.3 | 78.3(7.9) | 0.87(0.02) | -1.9 |
l-C3H ![]() |
≤4.8 | ≤5.3 | 8.5(1.5) | 0.31(0.05) | -2.0 | ||||
l-C3H ![]() |
≤4.8 | 15.0(2.5) | 0.83(0.13) | 11.1 | 9.8(1.7) | 0.38(0.05) | -2.0 | ||
l-C3H ![]() |
≤4.8 | 10.7(1.9) | 0.51(0.09) | 11.1 | 9.8(1.8) | 0.45(0.05) | -2.1 | ||
33 SO 23 – 12 F=![]() ![]() |
≤4.8 | 10.9(2.1) | 0.62(0.08) | 11.2 | ≤4.3 | ||||
SO NJ 23 – 12 | 780.9 (78.1) | 0.69(0.02) | -5.0 | 1429.4(143.0) | 0.63(0.01) | 11.2 | 328.4(32.9) | 0.45(0.01) | -2.0 |
NS+ 2–1 | 6.6(1.8) | 0.62(0.14) | -5.3 | ≤5.3 | ≤4.3 | ||||
CH3SH 40,4,0 – 30,3,0 | 6.9(1.5) | 0.38(0.11) | -5.1 | ≤5.3 | 7.2(1.7) | 0.52(0.10) | -2.0 | ||
CH3SH 41,3,1 – 31,2,1 | 7.9(1.7) | 0.50(0.09) | -5.0 | ≤5.3 | ≤4.3 | ||||
o-H2C34S | ≤4.8 | ≤4.3 | 6.8(1.6) | 0.41(0.07) | -1.9 | ||||
o-H2CS | 37.8(4.0) | 0.61(0.02) | -5.0 | 58.2(6.0) | 0.55(0.02) | 11.2 | 111.2(11.2) | 0.39(0.01) | -2.0 |
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