2011.0.00471.S/2011.0.00471.S_2012-05-29/2011.0.00471.S_2012-05-29/sg_ouss_id/group_ouss_id/member_ouss_id/calibrated

full summary of this dataset can be found here

Spectral setup

SpwIDFrame#chanskyfreq(MHz)Chwid(kHz)BW(MHz)beam("x" deg)
0TOPO384097422.8 ~ 98360.1244.141937.5000002.4 x 1.6, 68.6
1TOPO384098463.9 ~ 99401.1244.141937.5000002.4 x 1.6, 67.3
2TOPO384085937.4 ~ 86874.6244.141937.5000002.8 x 1.8, 69.3
3TOPO384088354.1 ~ 89291.3244.141937.5000002.7 x 1.8, 70.5

Observed fields

FieldIDFieldNameR.A.DecEpochnRows
0J0538-44005:38:50.361000-44.05.08.93900J200055080
1J0637-75206:35:46.507000-75.16.16.81500J200045900
330_Doradus05:38:44.488191-69.04.12.94344J200073440
430_Doradus05:38:49.407087-69.04.12.92004J200073440
530_Doradus05:38:42.032531-69.04.35.74914J200073440
630_Doradus05:38:46.951427-69.04.35.72573J200073440
730_Doradus05:38:51.870323-69.04.35.70232J200073440
830_Doradus05:38:44.495768-69.04.58.53142J200073440
930_Doradus05:38:49.414664-69.04.58.50801J200073440


Spectral window: 0

Lovas recommendation (http://physics.nist.gov/cgi-bin/micro/table5/start.pl)

click table head to collapse/expand

Rest frequency (MHz)Molecular transition
97535.908g-CH3CH2OH 21(1,21)-21(0,21) t=1-0
97536.849g-CH3CH2OH 23(1,23)-23(0,23) t=1-0
97546.875g-CH3CH2OH 29(1,28)-29(2,28) t=1-0
97549.692g-CH3CH2OH 26(0,26)-26(1,26) t=1-0
97562.844g-CH3CH2OH 24(1,24)-24(0,24) t=1-0
97569.000unidentified
97574.042g-CH3CH2OH 20(1,20)-20(0,20) t=1-0
97577.278CH3OCHO 8(5,3)-7(5,2) E t=1
97577.900unidentified
97582.808CH3OH 2(1,1)-1(1,0) A--
97597.180CH3OCHO 8(3,6)-7(3,5) A t=1
97600.390g-CH3CH2OH 25(1,25)-25(0,25) t=1-0
97603.000unidentified
97618.700unidentified
97631.329g-CH3CH2OH 27(0,27)-27(1,27) t=1-0
97632.700H213CS 3(1,3)-2(1,2)
97649.502g-CH3CH2OH 19(1,19)-19(0,19) t=1-0
97651.392CH3OCHO 10(4,7)-10(3,8) E
97661.356CH3OCHO 8(4,5)-7(4,4) A t=1
97662.000unidentified
97672.030CH313CH2CN 11(2,10)-10(2,9)
97678.260CH3OH 21(6,16)-22(5,17) A--
97679.380CH3OH 21(6,15)-22(5,18) A++
97694.197CH3OCHO 10(4,7)-10(3,8) A
97702.340SO2 7(3,5)-8(2,6)
97715.40134SO N,J=2,3-1,2
97729.400unidentified
97738.762CH3OCHO 8(6,3)-7(6,2) E t=1
97739.300unidentified
97752.824CH3OCHO 8(4,4)-7(4,3) A t=1
97753.400unidentified
97755.610g-CH3CH2OH 28(1,28)-28(0,28) t=1-0
97774.307g-CH3CH2OH 18(1,18)-18(0,18) t=1-0
97815.987g-CH3CH2OH 29(1,29)-29(0,20) t=1-0
97833.634H2CCCC 11(1,11)-10(1,10)
97846.300unidentified
97862.540C5H 21/2 J=41/2-39/2 e
97868.730C5H 21/2 J=41/2-39/2 f
97869.800unidentified
97874.000unidentified
97885.626CH3OCHO 8(5,4)-7(5,3) E t=1
97886.000unidentified
97897.129CH3OCHO 8(4,4)-7(4,3) E t=1
97897.500unidentified
97915.600unidentified
97926.000unidentified
97931.200unidentified
97932.445g-CH3CH2OH 31(0,31)-31(1,31) t=1-0
97957.200unidentified
97962.858g-CH3CH2OH 17(1,17)-17(0,17) t=1-0
97980.953CS 2-1
97995.212l-C3H 21/2 J=9/2-7/2 F=5-4e
97995.951l-C3H 21/2 J=9/2-7/2 F=4-3e
98011.649l-C3H 21/2 J=9/2-7/2 F=5-4f
98012.576l-C3H 21/2 J=9/2-7/2 F=4-3f
98030.400CH3OH 24(6,19)-23(7,16) A--
98030.440CH3OH 24(6,18)-23(7,17) A++
98033.907CH3CH213CN 11(7,*)-10(7,*)
98039.612CH313CH2CN 11(7,*)-10(7,*)
98040.565CH313CH2CN 11(6,*)-10(6,*)
98042.563CH3CH213CN 11(5,*)-10(5,*)
98052.969CH313CH2CN 11(5,*)-10(5,*)
98056.191CH313CH2CN 11(9,*)-10(9,*)
98060.000unidentified
98072.727CH3CH213CN 11(4,8)-10(4,7)
98074.628CH3CH213CN 11(4,7)-10(4,6)
98087.345CH313CH2CN 11(4,8)-10(4,7)
98089.684CH313CH2CN 11(4,7)-10(4,6)
98117.426CH3CH213CN 11(3,9)-10(3,8)
98134.865CH313CH2CN 11(3,9)-10(3,8)
98153.787SiC4 32-31
98165.34613CH3CH2CN 11(1,10)-10(1,9)
98177.578CH3CH2CN 11(2,10)-10(2,9)
98182.199CH3OCHO 8(7,1)-7(7,0) E
98190.653CH3OCHO 8(7,1)-7(7,0) A
98190.653CH3OCHO 8(7,2)-7(7,1) A
98191.414CH3OCHO 8(7,2)-7(7,1) E
98218.353H2CCCC 11(3,9)-10(3,8)
98218.355H2CCCC 11(3,8)-10(3,7)
98230.313g-CH3CH2OH 16(1,16)-16(0,16) t=1-0
98238.285H2CCCC 11(2,9)-10(2,8)
98244.941H2CCCC 11(0,11)-10(0,10)
98257.700unidentified
98265.900unidentified
98268.515CCCS 17-16
98270.369CH3OCHO 8(6,2)-7(6,1) E
98278.870CH3OCHO 8(6,3)-7(6,2) E
98279.746CH3OCHO 8(6,3)-7(6,2) A
98279.788CH3OCHO 8(6,2)-7(6,1) A
98333.900unidentified
98351.900unidentified

Spectral window: 1

Lovas recommendation (http://physics.nist.gov/cgi-bin/micro/table5/start.pl)

click table head to collapse/expand

Rest frequency (MHz)Molecular transition
98474.55033SO N,J=2,3-1,2 F=3/2-1/2
98482.15033SO N,J=2,3-1,2 F=5/2-3/2
98489.08033SO N,J=2,3-1,2 F=7/2-5/2
98493.68033SO N,J=2,3-1,2 F=9/2-7/2
98512.519HC5N 37-36
98523.881CH3CH2CN 11(6)-10(6)
98524.663CH3CH2CN 11(7)-10(7)
98524.690C5H 23/2 J=41/2-39/2 f
98527.190C5H 23/2 J=41/2-39/2 e
98532.075CH3CH2CN 11(8)-10(8)
98533.983CH3CH2CN 11(5)-10(5)
98544.152CH3CH2CN 11(9,*)-10(9,*)
98564.832CH3CH2CN 11(4,8)-10(4,7)
98566.797CH3CH2CN 11(4,7)-10(4,6)
98606.771CH3OCHO 8(3,6)-7(3,5) E
98610.104CH3CH2CN 11(3,9)-10(3,8)
98611.195CH3OCHO 8(3,6)-7(3,5) A
98630.000unidentified
98651.514(CH3)2CO 5(5,1)-4(4,1) EE
98655.097H2CCCC 11(1,10)-10(1,9)
98663.000unidentified
98682.635CH3OCHO 8(4,5)-7(4,4) A
98696.000unidentified
98701.106CH3CH2CN 11(3,8)-10(3,7)
98711.931CH3OCHO 8(4,5)-7(4,4) E
98747.797CH3OCHO 8(4,4)-7(4,3) E
98771.000unidentified
98792.314CH3OCHO 8(4,4)-7(4,3) A
98800.980(CH3)2CO 5(5,0)-4(4,0) EE
98863.314CH3CHO 5(1,4) - 4(1,3) E
98875.160CH3OCHO 11(4,8)-11(3,9) A
98900.951CH3CHO 5(1,4) - 4(1,3) A--
98926.723AlF 3-2
98940.020CCCN 10-9 J=21/2-19/2
98958.780CCCN 10-9 J=19/2-17/2
98976.278SO2 28(7,21)-29(6,24)
99011.000unidentified
99068.000unidentified
99083.405C6H 21/2 J=71/2-69/2 f
99087.000unidentified
99118.600NH2D 5(2,4)-4(1,4)
99120.000unidentified
99128.097C6H- 36-35
99134.046C6H 21/2 J=71/2-69/2 e
99143.725g-CH3CH2OH 27(2,26)-27(1,26) t=1-0
99172.534CH3CH213CN 11(2,9)-10(2,8)
99203.460CH3SH 2(1)-2(0) E
99264.980CH3SH 3(1)-3(0) E
99299.905SO N,J=2,3-1,2
99311.195NH2CN 5(1,5)-4(1,4)
99324.358CH3OCH3 4(1,4)-3(0,3) EA+AE
99325.208CH3OCH3 4(1,4)-3(0,3) EE
99326.058CH3OCH3 4(1,4)-3(0,3) AA
99361.000unidentified
99378.000unidentified
99392.526SO2 29(4,26)-28(5,23)

Spectral window: 2

Lovas recommendation (http://physics.nist.gov/cgi-bin/micro/table5/start.pl)

click table head to collapse/expand

Rest frequency (MHz)Molecular transition
85939.100unidentified
85943.000unidentified
85945.968CH2CHCN 9(8,*)-8(8,*) 2v11
85973.249CH3OCH3 13(2,12)-12(3,9) AA
85976.131CH3OCH3 13(2,12)-12(3,9) EE
85979.002CH3OCH3 13(2,12)-12(3,9) EA
85979.025CH3OCH3 13(2,12)-12(3,9) AE
85987.176CH2CHCN 9(2,7)-8(2,6) 1v11
86010.000unidentified
86021.008CH3OCHO 7(5,2)-6(5,1) E
86027.674CH3OCHO 7(5,3)-6(5,2) E
86029.445CH3OCHO 7(5,3)-6(5,2) A
86030.212CH3OCHO 7(5,2)-6(5,1) A
86034.300unidentified
86048.500C4H 2S J=9-8 2v7 L
86054.967HC15N 1-0
86074.274CH3NH2 4(1)A2 -4(0)A1 F=3-3
86074.498CH3NH2 4(1)A2 -4(0)A1 F=5-5
86075.369CH3NH2 4(1)A2 -4(0)A1 F=4-4
86093.983SO N,J=2,2-1,1
86104.440C4H 2S J=9-8 2v7 U
86133.200unidentified
86148.000unidentified
86151.600unidentified
86181.413CCS N,J=7,6-6,5
86204.600unidentified
86207.800unidentified
86210.079CH3OCHO 7(4,4)-6(4,3) A
86220.900unidentified
86223.548CH3OCHO 7(4,3)-6(4,2) E
86223.780CH3OCH3 2(2,0)-2(1,1) AE
86224.106CH3OCHO 7(4,4)-6(4,3) E
86225.615CH3OCH3 2(2,0)-2(1,1) EA
86226.727CH3OCH3 2(2,0)-2(1,1) EE
86228.720CH3OCH3 2(2,0)-2(1,1) AA
86239.600unidentified
86243.430SiO 2-1 v=1
86243.500unidentified
86248.200unidentified
86250.576CH3OCHO 7(4,3)-6(4,2) A
86254.848CH2CHCN 9(2,7)-8(2,6) 2v11
86259.700unidentified
86263.100unidentified
86263.500unidentified
86265.826CH3OCHO 7(3,5)-6(3,4) A
86268.659CH3OCHO 7(3,5)-6(3,4) E
86291.800unidentified
86297.200unidentified
86300.500unidentified
86300.700unidentified
86311.267g-CH3CH2OH 5(2,4)-4(2,3) t=0-0
86312.700unidentified
86317.000unidentified
86338.736H13CN 1-0 F=1-1
86340.176H13CN 1-0 F=2-1
86342.255H13CN 1-0 F=0-1
86369.100unidentified
86378.200unidentified
86381.831NH2CHO 7(1,6)-7(0,7) F=7-7
86382.751NH2CHO 7(1,6)-7(0,7)
86383.130NH2CHO 7(1,6)-7(0,7) F=8-8
86383.318NH2CHO 7(1,6)-7(0,7) F=6-6
86386.300unidentified
86389.200unidentified
86389.200unidentified
86395.800unidentified
86398.474CH3CH213CN 10(1,10)-9(1,9)
86398.600unidentified
86398.800unidentified
86416.900unidentified
86421.800unidentified
86440.200unidentified
86445.800unidentified
86458.271CH2DCN 5(1,5)-4(1,4)
86459.300unidentified
86473.000unidentified
86473.400unidentified
86481.000unidentified
86484.212CH3CH2CN 29(3,27)-28(4,24)
86486.600unidentified
86492.970HCOOD 4(0,4)-3(0,3)
86536.600unidentified
86543.700unidentified
86546.180HCOOH 4(1,4)-3(1,3)
86555.912g-CH3CH2OH 5(4,2)-4(4,1) t=0-0
86556.012g-CH3CH2OH 5(4,1)-4(4,0) t=0-0
86557.564s-CH2CHOH 2(1,2)-1(0,1)
86562.780Si13CC 4(1,4)-3(1,3)
86570.249C7H 21/2 99/2-97/2 f
86593.687CCCO 9-8
86604.292g-CH3CH2OH 5(3,3)-4(3,2) t=0-0
86615.602CH3OH 7(2,6)-6(3,3) A--
86617.74229Si34S 5-4
86621.734g-CH3CH2OH 5(3,2)-4(3,2) t=0-0
86639.095SO2 8(3,5)-9(2,8)
86650.849CH2CHCH3 5(0,5)-4(0,4) E
86651.584CH2CHCH3 5(0,5)-4(0,4) A
86670.820HCO 1(0,1)-0(0,0) 3/2-1/2 F=2-1
86708.350HCO 1(0,1)-0(0,0) 3/2-1/2 F=1-0
86708.374CCCS 15-14
86745.317CH3CH2CN 8(1,8)-7(0,7)
86754.288H13CO+ 1-0
86777.430HCO 1(0,1)-0(0,0) 1/2-1/2 F=1-1
86781.400unidentified
86784.500unidentified
86794.500unidentified
86803.600unidentified
86805.750HCO 1(0,1)-0(0,0) 1/2-1/2 F=0-1
86812.300unidentified
86814.388CH2DCN 5(4,*)-4(4,*)
86819.848CH3CH2CN 10(1,10)-9(1,9)
86824.595CH2DCN 5(3,3)-4(3,2)
86824.597CH2DCN 5(3,2)-4(3,1)
86831.480CH3SH 13(3)-14(2) A++
86833.932CH2DCN 5(0,5)-4(0,4)
86846.995SiO 2-1 v=0
86864.000unidentified

Spectral window: 3

Lovas recommendation (http://physics.nist.gov/cgi-bin/micro/table5/start.pl)

click table head to collapse/expand

Rest frequency (MHz)Molecular transition
88358.420CH3OCHO 22(5,17)-22(4,18) A
88402.000unidentified
88445.000unidentified
88481.000unidentified
88540.600unidentified
88594.809CH3OH 15(3,13)-14(4,10) A++
88630.415HCN 1-0 F=1-1
88631.847HCN 1-0 F=2-1
88633.936HCN 1-0 F=0-1
88667.901CH3NH2 2(0)B1 -1(0)B2
88668.681CH3NH2 2(0)E2+1 -1(0)E2+1
88669.543CH3NH2 2(0)E1+1 -1(0)E1+1
88669.626CH3NH2 2(0)A1 -1(0)A2
88706.220CH3OCH3 15(2,13)-15(1,14) EA+AE
88707.701CH3OCH3 15(2,13)-15(1,14) EE
88709.181CH3OCH3 15(2,13)-15(1,14) AA
88720.56734SO2 7(3,5)-8(2,6)
88723.239CH3OCHO 11(3,9)-11(2,10) A
88741.800unidentified
88749.800unidentified
88758.419CH3CH2CN 27(3,24)-27(2,25)
88765.500unidentified
88770.800unidentified
88843.117CH3OCHO 7(1,6)-6(1,5) E
88851.641CH3OCHO 7(1,6)-6(1,5) A
88855.080CH3CH213CN 10(2,9)-9(2,8)
88861.000unidentified
88865.692H15NC 1-0
88913.850C5H 23/2 J=37/2-35/2 f
88915.940C5H 23/2 J=37/2-35/2 e
88916.000unidentified
88939.993CH3OH 15(3,12)-14(4,11) A--
88940.238H2CCCC 10(1,10)-9(1,9)
88957.000unidentified
88977.000unidentified
89043.500unidentified
89045.590CCCN 9-8 J=19/2-17/2
89060.827t-CH3CH2OH 18(4,14)-17(5,13)
89064.360CCCN 9-8 J=17/2-15/2
89082.200unidentified
89084.000unidentified
89086.423HCN 1-0 F=1-1 (0,2,0)=0
89087.914HCN 1-0 F=2-1 (0,2,0)=0
89090.130HCN 1-0 F=0-1 (0,2,0)=0
89093.200unidentified
89103.72029SiS 5-4
89104.300HC7N 79-78
89116.025CH3CH213CN 10(6,*)-9(6,*)
89118.949CH3CH213CN 10(7,*)-9(7,*)
89121.504CH3CH213CN 10(5,*)-9(5,*)
89122.297CH313CH2CN 10(6,*)-9(6,*)
89123.590CH313CH2CN 10(7,*)-9(7,*)
89129.913CH313CH2CN 10(5,*)-9(5,*)
89130.350CH313CH2CN 10(8,*)-9(8,*)
89142.905CH3CH213CN 10(4,7)-9(4,6)
89143.857CH3CH213CN 10(4,6)-9(4,5)
89154.617CH313CH2CN 10(4,7)-9(4,6)
89155.789CH313CH2CN 10(4,6)-9(4,5)
89188.526HCO+ 1-0
89234.000unidentified
89235.656CH3CH213CN 10(3,7)-9(3,6)
89251.160CH2DOH 2(0,2)-1(0,1) o1
89259.143CH313CH2CN 10(3,7)-9(3,6)
89275.410CH2DOH 2(0,2)-1(0,1) e1

uv sampling

FieldIDSpwIDuv_min(klambda)uv_max(klambda)
0025.009361.357
0125.009361.356
0225.012361.334
0325.009361.351
1025.404353.677
1125.400353.666
1225.419353.620
1325.407353.653
3024.348372.823
3124.344372.795
3224.339372.752
3324.350373.029
4023.166360.704
4123.160360.702
4223.198360.647
4323.178360.553
5021.546366.897
5121.547366.840
5221.549366.826
5321.545366.964
6021.522355.379
6121.523355.381
6221.526355.382
6321.521355.365
7023.081360.991
7123.075360.991
7223.113360.990
7323.092360.993
8021.040372.926
8121.040372.906
8221.041372.875
8321.039373.075
9021.200361.505
9121.201361.505
9221.202361.505
9321.200361.507

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