UCI FJX v7.3c = 7.3b + new integral weighting of solar and Rayleigh
NEW FMT: Jshort(a6)|Jlong(a16)|Notes, including q's. T or p at begin of block
   18 NWWW   27 NSSS 18 J-bins, reads J's (1-3 Xsect blks interp T or 'p'(until 'endofJ')
w-eff |wavelength (nm) | SPhot wtd, FJ#18 cuts at 778nm
          187.      191.      193.      196.      202.      208.
          211.      214.      261.      267.      277.      295.
          303.      310.      316.      333.      383.      599.
SPhot |solar #/cm2/s   | SUSIM average 11Nov94(low) + 29Mar92(med-high)
    a 1.391E+12 1.627E+12 1.664E+12 9.278E+11 7.842E+12 4.680E+12 solflx
    b 9.918E+12 1.219E+13 6.364E+14 4.049E+14 3.150E+14 5.893E+14 solflx
    c 7.670E+14 5.041E+14 8.895E+14 3.852E+15 1.547E+16 1.805E+17 solflx
SWatt |solarheat W/m2  | ASTM, scaled=1360.8 W/m2 (Kopp&Lean 2011)
    a   0.01473   0.01684   0.01702   0.00937   0.07664   0.04450 solarw
    b   0.09299   0.11278     4.818     2.962     2.218     3.703 solarw
    c     4.670     3.063     5.414     22.28     77.17    608.68 solarw
Y-PAR |photosyn act rad| Mccree 1972ab PAR spectrum
    a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Y-PAR
    b 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Y-PAR
    c 0.000E+00 0.000E+00 0.000E+00 5.138E-02 4.855E-01 6.760E-01 Y-PAR
Raylay|Rayleigh Scatter| flux weighted mean cross sections (cm^2)
    a 5.073E-25 4.479E-25 4.196E-25 3.906E-25 3.355E-25 2.929E-25 Raylay
    b 2.736E-25 2.581E-25 1.049E-25 9.492E-26 8.103E-26 6.135E-26 Raylay
    c 5.424E-26 4.925E-26 4.516E-26 3.644E-26 2.082E-26 4.427E-27 Raylay
O2    |O2=O+O          | JPL10
 180a 1.727E-21 1.989E-22 3.004E-23 9.833E-24 7.306E-24 6.827E-24 O2
 180b 6.238E-24 5.748E-24 1.153E-25 5.030E-25 4.150E-25 0.000E+00 O2
 180c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 O2
O2    |
 260a 2.273E-21 3.070E-22 4.943E-23 1.408E-23 7.688E-24 6.827E-24 O2
 260b 6.238E-24 5.888E-24 1.153E-25 5.030E-25 4.150E-25 0.000E+00 O2
 260c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 O2
O2    |
 300a 2.763E-21 4.269E-22 7.478E-23 2.100E-23 8.350E-24 6.827E-24 O2
 300b 6.238E-24 5.994E-24 1.153E-25 5.030E-25 4.150E-25 0.000E+00 O2
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 O2
O3    |O3-total        | JPl10+IUPAC 2/2013
 218a 5.988E-19 4.859E-19 4.307E-19 3.654E-19 3.410E-19 4.849E-19 O3
 218b 6.534E-19 9.320E-19 8.757E-18 3.513E-18 1.508E-18 7.925E-19 O3
 218c 2.456E-19 8.904E-20 3.661E-20 4.539E-21 6.167E-23 1.967E-21 O3
O3    |
 258a 5.989E-19 4.862E-19 4.314E-19 3.666E-19 3.421E-19 4.845E-19 O3
 258b 6.519E-19 9.299E-19 8.826E-18 3.566E-18 1.547E-18 8.260E-19 O3
 258c 2.617E-19 9.739E-20 4.139E-20 5.515E-21 6.167E-23 1.967E-21 O3
O3    |
 298a 5.990E-19 4.866E-19 4.320E-19 3.678E-19 3.432E-19 4.840E-19 O3
 298b 6.504E-19 9.278E-19 8.896E-18 3.618E-18 1.586E-18 8.595E-19 O3
 298c 2.778E-19 1.058E-19 4.617E-20 6.493E-21 6.167E-23 1.967E-21 O3
O3(1D)|Qyld O3=O(1D)+O2| JPL10 3/2013
 200a 4.842E-01 4.922E-01 5.071E-01 5.228E-01 6.040E-01 6.803E-01 O3(1D)
 200b 7.190E-01 7.549E-01 9.000E-01 8.989E-01 8.929E-01 9.000E-01 O3(1D)
 200c 8.901E-01 4.130E-01 8.985E-02 6.782E-02 0.000E+00 0.000E+00 O3(1D)
O3(1D)|
 260a 4.843E-01 4.922E-01 5.072E-01 5.229E-01 6.040E-01 6.802E-01 O3(1D)
 260b 7.189E-01 7.549E-01 9.000E-01 8.989E-01 8.929E-01 9.000E-01 O3(1D)
 260c 8.916E-01 4.656E-01 1.417E-01 6.995E-02 0.000E+00 0.000E+00 O3(1D)
O3(1D)|
 320a 4.843E-01 4.922E-01 5.072E-01 5.229E-01 6.040E-01 6.805E-01 O3(1D)
 320b 7.189E-01 7.550E-01 9.000E-01 8.989E-01 8.929E-01 9.000E-01 O3(1D)
 320c 8.967E-01 5.852E-01 2.919E-01 7.943E-02 0.000E+00 0.000E+00 O3(1D)
NO    |NO=N+O          |delta(1,0)&(0,0) scaled by 0.6 (WACCM in PhotoComp2008)
x298a 6.054E-19 6.936E-19 3.475E-19 0.000E+00 0.000E+00 0.000E+00 NO
 298b 0.000E+00 8.892E-21 0.000E+00 0.000E+00 0.000E+00 0.000E+00 NO
 298c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 NO
H2COa |H2CO=>H+HCO     | JPL10
 223a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 H2COa
 223b 0.000E+00 0.000E+00 3.143E-21 1.021E-20 1.269E-20 2.323E-20 H2COa
 223c 2.498E-20 1.133E-20 2.183E-20 4.746E-21 0.000E+00 0.000E+00 H2COa
H2COa |
 298a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 H2COa
 298b 0.000E+00 0.000E+00 3.147E-21 1.018E-20 1.266E-20 2.315E-20 H2COa
 298c 2.497E-20 1.131E-20 2.189E-20 4.751E-21 0.000E+00 0.000E+00 H2COa
H2COb |H2CO=>H2+CO     | JPL10
 223a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 H2COb
 223b 0.000E+00 0.000E+00 3.642E-21 5.787E-21 5.316E-21 8.181E-21 H2COb
 223c 7.917E-21 4.011E-21 1.081E-20 1.082E-20 2.088E-22 0.000E+00 H2COb
H2COb |
 298a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 H2COb
 298b 0.000E+00 0.000E+00 3.649E-21 5.768E-21 5.305E-21 8.154E-21 H2COb
 298c 7.914E-21 4.002E-21 1.085E-20 1.085E-20 2.081E-22 0.000E+00 H2COb
H2O2  |H2O2=>OH+OH     | JPL10
 200a 2.325E-19 4.629E-19 5.394E-19 5.429E-19 4.447E-19 3.755E-19 H2O2
 200b 3.457E-19 3.197E-19 5.346E-20 4.855E-20 3.423E-20 8.407E-21 H2O2
 200c 5.029E-21 3.308E-21 2.221E-21 8.598E-22 1.807E-23 0.000E+00 H2O2
H2O2  |
 300a 2.325E-19 4.629E-19 5.394E-19 5.429E-19 4.447E-19 3.755E-19 H2O2
 300b 3.457E-19 3.197E-19 5.465E-20 4.966E-20 3.524E-20 9.354E-21 H2O2
 300c 5.763E-21 3.911E-21 2.718E-21 1.138E-21 2.419E-23 0.000E+00 H2O2
CH3OOH|CH3OOH=>CH3O+OH |
 298a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 3.120E-19 CH3OOH
 298b 2.882E-19 2.250E-19 2.716E-20 2.740E-20 2.143E-20 5.624E-21 CH3OOH
 298c 3.520E-21 2.403E-21 1.697E-21 7.230E-22 6.973E-23 0.000E+00 CH3OOH
NO2   |NO2=>NO+O       | JPL10
 200a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 NO2
 200b 0.000E+00 0.000E+00 1.835E-20 4.693E-20 7.705E-20 1.078E-19 NO2
 200c 1.470E-19 1.832E-19 2.181E-19 3.138E-19 4.321E-19 1.636E-22 NO2
NO2   |
 294a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 NO2
 294b 0.000E+00 0.000E+00 2.313E-20 4.694E-20 7.553E-20 1.063E-19 NO2
 294c 1.477E-19 1.869E-19 2.295E-19 3.448E-19 4.643E-19 5.130E-22 NO2
NO3   |NO3=NO2+O/NO+O2 | JPL10, calculated q(NO2+O)=0.882, q(NO+O2)=0.112
 190a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 NO3
 190b 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 NO3
 190c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 5.294E-21 1.313E-18 NO3
NO3   |
 298a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 NO3
 298b 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 NO3
 298c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 3.796E-21 1.029E-18 NO3
N2O5  |N2O5=>NO2+NO3   | JPL10
 233a 0.000E+00 0.000E+00 8.922E-19 1.183E-18 5.868E-18 4.682E-18 N2O5
 233b 3.395E-18 2.613E-18 2.138E-19 2.155E-19 1.988E-19 3.772E-20 N2O5
 233c 2.182E-20 1.334E-20 8.419E-21 2.621E-21 1.313E-22 1.368E-25 N2O5
N2O5  |
 300a 0.000E+00 0.000E+00 1.078E-18 1.429E-18 7.088E-18 5.655E-18 N2O5
 300b 4.101E-18 3.156E-18 2.606E-19 2.645E-19 2.454E-19 5.154E-20 N2O5
 300c 3.210E-20 2.135E-20 1.468E-20 5.902E-21 6.002E-22 1.523E-24 N2O5
HNO2  |HONO=>OH+NO     | JPL10
 300a 9.693E-19 1.387E-18 1.574E-18 1.808E-18 2.154E-18 2.188E-18 HNO2
 300b 2.079E-18 1.911E-18 1.171E-19 1.849E-19 1.489E-19 5.487E-21 HNO2
 300c 9.353E-21 1.895E-20 3.195E-20 9.008E-20 6.900E-20 0.000E+00 HNO2
HNO3  |HONO2=>OH+NO2   | JPL10
 200a 4.169E-18 8.113E-18 8.882E-18 8.211E-18 3.777E-18 1.288E-18 HNO3
 200b 6.882E-19 4.998E-19 1.611E-20 1.794E-20 1.848E-20 3.383E-21 HNO3
 200c 1.374E-21 5.442E-22 2.087E-22 2.118E-23 8.193E-26 0.000E+00 HNO3
HNO3  |
 300a 4.284E-18 8.419E-18 9.368E-18 9.112E-18 4.462E-18 1.551E-18 HNO3
 300b 8.426E-19 5.852E-19 1.855E-20 2.162E-20 2.299E-20 4.371E-21 HNO3
 300c 1.920E-21 8.312E-22 3.573E-22 4.706E-23 2.539E-25 0.000E+00 HNO3
HNO4  |HO2NO2=>HO2+NO2 | JPL10 & scaled 1-micron J added to last bin
 300a 4.631E-18 7.576E-18 8.407E-18 7.479E-18 4.744E-18 2.854E-18 HNO4
 300b 2.217E-18 1.843E-18 2.799E-19 2.210E-19 1.539E-19 2.685E-20 HNO4
 300c 1.171E-20 5.683E-21 3.102E-21 8.269E-22 1.309E-23 5.542E-23 HNO4
ClNO3a|ClNO3=Cl+NO3    | JPL10
x200a 3.222E-19 7.351E-19 9.688E-19 1.664E-18 1.614E-18 1.774E-18 ClNO3a
 200b 1.921E-18 2.009E-18 1.948E-19 2.801E-19 2.046E-19 2.043E-20 ClNO3a
 200c 1.088E-20 6.655E-21 4.564E-21 2.324E-21 9.207E-22 8.211E-24 ClNO3a
ClNO3a|
x300a 3.527E-19 8.041E-19 1.055E-18 1.815E-18 1.705E-18 1.805E-18 ClNO3a
 300b 1.928E-18 2.001E-18 2.319E-19 3.033E-19 2.140E-19 2.787E-20 ClNO3a
 300c 1.564E-20 1.002E-20 7.086E-21 3.404E-21 1.177E-21 1.164E-23 ClNO3a
ClNO3b|ClNO3=ClO+NO2   | JPL10
x200a 2.147E-19 4.899E-19 6.457E-19 1.109E-18 1.076E-18 1.183E-18 ClNO3b
 200b 1.281E-18 1.339E-18 1.299E-19 1.867E-19 1.364E-19 1.362E-20 ClNO3b
 200c 7.256E-21 4.187E-21 2.372E-21 7.063E-22 2.641E-23 0.000E+00 ClNO3b
ClNO3b|
x300a 2.351E-19 5.361E-19 7.034E-19 1.210E-18 1.136E-18 1.203E-18 ClNO3b
 300b 1.285E-18 1.334E-18 1.546E-19 2.022E-19 1.427E-19 1.858E-20 ClNO3b
 300c 1.043E-20 6.303E-21 3.680E-21 1.052E-21 3.330E-23 0.000E+00 ClNO3b
Cl2   |Cl2=>Cl+Cl      | JPL10
x200a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Cl2
 200b 0.000E+00 0.000E+00 5.482E-21 2.419E-20 4.980E-20 8.413E-20 Cl2
 200c 1.393E-19 1.878E-19 2.265E-19 2.524E-19 6.328E-20 8.221E-22 Cl2
Cl2
x300a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Cl2
 300b 0.000E+00 0.000E+00 6.002E-21 2.708E-20 5.409E-20 8.855E-20 Cl2
 300c 1.404E-19 1.844E-19 2.185E-19 2.411E-19 6.552E-20 8.055E-22 Cl2
HOCl  |HOCl=>OH+Cl     | JPL10
x300a 0.000E+00 3.695E-21 1.571E-20 2.435E-20 5.887E-20 5.424E-20 HOCl
 300b 5.798E-20 6.694E-20 1.019E-19 6.541E-20 5.430E-20 5.570E-20 HOCl
 300c 6.067E-20 5.955E-20 5.376E-20 3.120E-20 6.529E-21 1.503E-23 HOCl
OClO  |OClO=>O+ClO     | JPL10
x204a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 HOCl
 204b 0.000E+00 0.000E+00 4.061E-19 5.616E-19 8.776E-19 1.211E-18 HOCl
 204c 1.857E-18 2.606E-18 2.522E-18 4.227E-18 3.254E-18 4.794E-20 HOCl
Cl2O2 |ClOOCl=>ClO+ClO | JPL10
x220a 0.000E+00 2.177E-19 9.321E-19 1.435E-18 3.578E-18 3.009E-18 Cl2O2
 220b 2.648E-18 2.357E-18 4.063E-18 1.971E-18 1.236E-18 8.681E-19 Cl2O2
 220c 5.719E-19 4.163E-19 3.234E-19 1.921E-19 3.857E-20 7.238E-22 Cl2O2
ClO   |ClO=>Cl+O       | JPL10
x300a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 ClO
 300b 0.000E+00 0.000E+00 4.737E-18 3.262E-18 1.858E-18 1.428E-18 ClO
 300c 5.982E-19 3.548E-19 1.427E-19 0.000E+00 0.000E+00 0.000E+00 ClO
BrO   |BrO=>Br+O       | JPL10
x300a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 BrO
 300b 0.000E+00 0.000E+00 0.000E+00 5.620E-19 1.202E-18 2.008E-18 BrO
 300c 3.239E-18 4.520E-18 5.064E-18 5.809E-18 7.350E-19 0.000E+00 BrO
BrNO3 |BrONO2=>BrO+NO2 | JPL10
x200a 0.000E+00 0.000E+00 5.484E-19 7.245E-19 3.702E-18 3.475E-18 BrNO3
 200b 3.182E-18 2.978E-18 5.304E-19 6.086E-19 4.489E-19 1.963E-19 BrNO3
 200c 1.584E-19 1.307E-19 1.110E-19 8.033E-20 3.377E-20 1.499E-21 BrNO3
BrNO3
x300a 0.000E+00 0.000E+00 8.026E-19 1.071E-18 5.166E-18 4.190E-18 BrNO3
 300b 3.467E-18 3.039E-18 5.567E-19 5.989E-19 4.528E-19 2.098E-19 BrNO3
 300c 1.705E-19 1.425E-19 1.207E-19 8.648E-20 3.716E-20 1.706E-21 BrNO3
HOBr  |HOBr=>OH+Br     | JPL10
x300a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 HOBr
 300b 0.000E+00 0.000E+00 1.324E-19 2.011E-19 2.202E-19 2.196E-19 HOBr
 300c 1.726E-19 1.367E-19 1.157E-19 1.125E-19 6.197E-20 3.253E-21 HOBr
BrCl  |BrCl=>Br+Cl     | JPL10
x200a 0.000E+00 0.000E+00 3.138E-21 3.852E-21 2.798E-20 4.258E-20 BrCl
 200b 4.915E-20 5.482E-20 2.293E-20 1.531E-20 7.620E-21 1.983E-21 BrCl
 200c 4.115E-21 9.571E-21 2.126E-20 1.102E-19 3.272E-19 2.338E-20 BrCl
BrCl
x300a 0.000E+00 0.000E+00 3.356E-21 4.152E-21 2.906E-20 4.234E-20 BrCl
 300b 4.785E-20 5.244E-20 2.430E-20 1.596E-20 8.718E-21 3.854E-21 BrCl
 300c 7.582E-21 1.550E-20 3.038E-20 1.223E-19 3.184E-19 2.414E-20 BrCl
N2O   |N2O=>N2+O       | JPL10
x200a 1.076E-19 8.490E-20 6.974E-20 5.200E-20 2.171E-20 6.405E-21 N2O
 200b 3.097E-21 2.473E-21 3.308E-25 1.048E-23 4.114E-23 0.000E+00 N2O
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 N2O
N2O
x300a 1.225E-19 1.006E-19 8.493E-20 6.658E-20 3.135E-20 1.150E-20 N2O
 300b 6.282E-21 4.614E-21 1.501E-24 4.070E-23 1.173E-22 0.000E+00 N2O
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 N2O
CFCl3 |CFCl3=>CFCl2+Cl | CFC-11    JPL10
x220a 2.177E-18 1.608E-18 1.302E-18 9.616E-19 4.538E-19 1.638E-19 CFCl3
 220b 9.562E-20 7.113E-20 4.112E-23 7.026E-22 1.892E-21 0.000E+00 CFCl3
 220c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CFCl3
CFCl3
x298a 2.237E-18 1.652E-18 1.339E-18 9.882E-19 4.884E-19 2.026E-19 CFCl3
 298b 1.266E-19 9.361E-20 9.732E-23 1.289E-21 2.955E-21 0.000E+00 CFCl3
 298c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CFCl3
CF2Cl2|CF2Cl2=>CF2Cl+  | CFC-12   JPL10
x220a 7.001E-19 4.044E-19 2.780E-19 1.507E-19 4.142E-20 6.627E-21 CF2Cl2
 220b 2.876E-21 5.395E-21 2.698E-25 8.767E-24 3.338E-23 0.000E+00 CF2Cl2
 220c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CF2Cl2
CF2Cl2
x300a 1.012E-18 5.844E-19 4.020E-19 2.178E-19 6.291E-20 1.258E-20 CF2Cl2
 300b 5.959E-21 8.779E-21 8.279E-25 2.466E-23 8.261E-23 0.000E+00 CF2Cl2
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CF2Cl2
F113  |CF3CCl3=>       | CF3CCl3 = CFC-113    JPL10
x210a 1.061E-18 6.852E-19 4.983E-19 2.810E-19 8.627E-20 2.020E-20 F113
 210b 1.043E-20 1.272E-20 4.158E-24 6.808E-23 1.800E-22 0.000E+00 F113
 210c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F113
F113
x300a 9.495E-19 5.932E-19 4.317E-19 2.618E-19 9.300E-20 2.661E-20 F113
 300b 1.453E-20 1.395E-20 6.689E-24 1.046E-22 2.685E-22 0.000E+00 F113
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F113
F114  |CF3CFCl2=>      | CF3CFCl2 = CFC-114   JPL10
x210a 1.291E-19 5.656E-20 3.403E-20 1.585E-20 4.491E-21 9.317E-22 F114
 210b 4.480E-22 6.972E-22 9.733E-26 2.472E-24 6.812E-24 0.000E+00 F114
 210c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F114
F114
x300a 1.203E-19 5.566E-20 3.520E-20 1.825E-20 6.078E-21 1.642E-21 F114
 300b 8.743E-22 9.578E-22 2.385E-25 6.055E-24 1.608E-23 0.000E+00 F114
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F114
F115  |CF3CF2Cl=>      | CF3CF2Cl = CFC-115   JPL10
x300a 6.876E-21 2.986E-21 1.891E-21 1.018E-21 3.531E-22 1.124E-22 F115
 300b 6.079E-23 6.176E-23 5.728E-27 6.317E-25 1.345E-24 0.000E+00 F115
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F115
CCl4  |CCl4=>          | CCl4 = Carbon-tetrachloride   JPL10
x200a 3.610E-18 1.670E-18 1.100E-18 7.155E-19 6.122E-19 4.744E-19 CCl4
 200b 3.774E-19 2.864E-19 6.486E-22 7.133E-21 1.323E-20 0.000E+00 CCl4
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CCl4
CCl4
x300a 3.707E-18 1.712E-18 1.124E-18 7.237E-19 6.267E-19 5.208E-19 CCl4
 300b 4.392E-19 3.544E-19 1.614E-21 1.234E-20 1.854E-20 0.000E+00 CCl4
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CCl4
CH3Cl |CH3Cl=>CH3+Cl   | CH3Cl = Methyl chloride   JPL10
x200a 2.838E-19 1.310E-19 8.192E-20 3.940E-20 1.098E-20 2.102E-21 CH3Cl
 200b 9.710E-22 1.654E-21 1.353E-25 4.702E-24 1.424E-23 0.000E+00 CH3Cl
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH3Cl
CH3Cl
x300a 2.842E-19 1.308E-19 8.238E-20 4.125E-20 1.284E-20 3.135E-21 CH3Cl
 300b 1.619E-21 2.046E-21 2.691E-25 9.348E-24 2.828E-23 0.000E+00 CH3Cl
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH3Cl
MeCCl3|CH3CCl3=>CH3CCl2| CH3CCl3 = Methyl chloroform   JPL10
x200a 2.720E-18 2.025E-18 1.688E-18 1.354E-18 7.434E-19 3.348E-19 MeCCl3
 200b 2.026E-19 1.374E-19 5.478E-23 1.440E-21 4.133E-21 0.000E+00 MeCCl3
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MeCCl3
MeCCl3
x300a 2.722E-18 2.020E-18 1.680E-18 1.338E-18 7.420E-19 3.515E-19 MeCCl3
 300b 2.232E-19 1.574E-19 2.197E-22 2.618E-21 5.521E-21 0.000E+00 MeCCl3
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MeCCl3
CH2Cl2|CH2Cl2=>CH2Cl+Cl| CH2Cl2 = di-chloromethane   JPL10
x200a 1.091E-18 6.168E-19 4.117E-19 2.063E-19 5.999E-20 1.421E-20 CH2Cl2
 200b 7.370E-21 9.789E-21 4.003E-24 5.376E-23 1.269E-22 0.000E+00 CH2Cl2
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH2Cl2
CH2Cl2
x300a 9.995E-19 5.790E-19 3.970E-19 2.144E-19 7.138E-20 2.124E-20 CH2Cl2
 300b 1.203E-20 1.237E-20 7.640E-24 1.026E-22 2.385E-22 0.000E+00 CH2Cl2
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH2Cl2
CHF2Cl|CHF2Cl=>CHF2+Cl | CHF2Cl = HCFC-22    JPL10
x200a 7.852E-21 2.816E-21 1.551E-21 6.716E-22 1.891E-22 4.359E-23 CHF2Cl
 200b 2.467E-23 3.483E-23 0.000E+00 2.454E-27 4.684E-25 0.000E+00 CHF2Cl
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CHF2Cl
CHF2Cl
x300a 7.528E-21 2.775E-21 1.578E-21 7.386E-22 2.375E-22 6.207E-23 CHF2Cl
 300b 3.512E-23 4.089E-23 0.000E+00 3.494E-27 6.670E-25 0.000E+00 CHF2Cl
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CHF2Cl
F123  |CF3CCHCl2=>     | CF3CCHCl2 = HCFC-123  JPL10
x210a 9.371E-19 5.088E-19 3.401E-19 1.837E-19 6.049E-20 1.614E-20 F123
 210b 8.774E-21 9.599E-21 4.437E-24 6.935E-23 1.699E-22 0.000E+00 F123
 210c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F123
F123
x295a 1.037E-18 6.011E-19 4.213E-19 2.461E-19 8.860E-20 2.646E-20 F123
 295b 1.495E-20 1.438E-20 1.191E-23 1.409E-22 3.152E-22 0.000E+00 F123
 295c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F123
F141b |CH3CFCl2=>      | CH3CFCl2 = HCFC-141b    JPL10
x200a 1.165E-18 7.326E-19 5.257E-19 3.034E-19 9.839E-20 2.384E-20 F141b
 200b 1.224E-20 1.398E-20 2.005E-24 6.588E-23 2.015E-22 0.000E+00 F141b
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F141b
F141b
x300a 1.126E-18 7.466E-19 5.559E-19 3.448E-19 1.221E-19 3.303E-20 F141b
 300b 1.757E-20 1.737E-20 5.164E-24 1.146E-22 3.133E-22 0.000E+00 F141b
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F141b
F142b |CH3CF2Cl=>      | CH3CF2Cl = HCFC-142b    JPL10
x210a 2.253E-20 8.483E-21 4.768E-21 2.113E-21 6.068E-22 1.276E-22 F142b
 210b 6.211E-23 9.375E-23 0.000E+00 1.766E-25 8.252E-25 0.000E+00 F142b
 210c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F142b
F142b
x298a 2.842E-20 1.172E-20 6.981E-21 3.370E-21 1.059E-21 2.543E-22 F142b
 298b 1.303E-22 1.602E-22 0.000E+00 4.755E-25 1.964E-24 0.000E+00 F142b
 298c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 F142b
CH3Br |CH3Br=>CH3+Br   | CH3Br = Methyl bromide     JPL10
x200a 1.064E-18 4.918E-19 5.748E-19 6.814E-19 7.562E-19 6.868E-19 CH3Br
 200b 6.096E-19 5.216E-19 6.038E-21 3.133E-20 3.378E-20 9.878E-26 CH3Br
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH3Br
CH3Br
x300a 1.091E-18 5.041E-19 5.891E-19 6.986E-19 7.717E-19 6.999E-19 CH3Br
 300b 6.239E-19 5.378E-19 7.764E-21 3.424E-20 3.540E-20 7.365E-25 CH3Br
 300c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH3Br
H1211 |CF2ClBr=>       | CF2ClBr = halon 1211       JPL10
x200a 5.810E-19 6.607E-19 7.844E-19 9.493E-19 1.290E-18 1.385E-18 H1211
 200b 1.313E-18 1.181E-18 2.933E-20 8.981E-20 8.335E-20 2.038E-23 H1211
 200c 3.698E-24 1.109E-24 3.929E-25 5.010E-27 0.000E+00 0.000E+00 H1211
H1211
x300a 5.063E-19 5.757E-19 6.828E-19 8.271E-19 1.105E-18 1.166E-18 H1211
 300b 1.105E-18 9.995E-19 3.541E-20 8.319E-20 7.215E-20 1.068E-22 H1211
 300c 2.727E-23 8.654E-24 3.067E-24 3.910E-26 0.000E+00 0.000E+00 H1211
H1301 |CF3Br=>         | CF3Br = halon 1301         JPL10
x200a 6.268E-20 8.611E-20 9.979E-20 1.158E-19 1.400E-19 1.404E-19 H1301
 200b 1.282E-19 1.096E-19 6.655E-22 5.389E-21 6.890E-21 1.311E-25 H1301
 200c 1.580E-26 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 H1301
H1301
x300a 5.426E-20 7.273E-20 8.354E-20 9.598E-20 1.173E-19 1.227E-19 H1301
 300b 1.165E-19 1.047E-19 1.413E-21 7.024E-21 7.262E-21 4.028E-25 H1301
 300c 4.856E-26 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 H1301
H2402 |CF2BrCF2Br=>    | CF2BrCF2Br = halon 2402    JPL10
x200a 1.038E-18 1.137E-18 1.167E-18 1.193E-18 1.145E-18 1.013E-18 H2402
 200b 9.185E-19 8.183E-19 1.999E-20 6.373E-20 5.698E-20 2.284E-24 H2402
 200c 6.437E-25 2.441E-25 1.156E-25 1.879E-27 0.000E+00 0.000E+00 H2402
H2402
x300a 1.023E-18 1.133E-18 1.175E-18 1.221E-18 1.213E-18 1.101E-18 H2402
 300b 1.008E-18 9.029E-19 2.581E-20 7.236E-20 6.360E-20 4.568E-23 H2402
 300c 1.287E-23 4.881E-24 2.311E-24 3.757E-26 0.000E+00 0.000E+00 H2402
CH2Br2|CH2Br2=>        | CH2Br2 = dibromo methane    JPL10
 200a 2.106E-18 2.100E-18 2.205E-18 2.384E-18 2.343E-18 2.413E-18 CH2Br2
 200b 2.691E-18 3.182E-18 1.489E-19 4.916E-19 3.187E-19 5.186E-23 CH2Br2
 200c 8.043E-24 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH2Br2
CH2Br2
 300a 1.983E-18 1.977E-18 2.076E-18 2.244E-18 2.206E-18 2.272E-18 CH2Br2
 300b 2.404E-18 2.561E-18 1.724E-19 3.708E-19 2.349E-19 2.670E-22 CH2Br2
 300c 4.141E-23 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH2Br2
CHBr3 |CHBr3=>         | CHBr3 = bromoform   JPL10
 210a 5.928E-18 4.527E-18 4.157E-18 3.943E-18 4.498E-18 4.775E-18 CHBr3
 210b 5.072E-18 5.503E-18 7.881E-19 9.160E-19 5.449E-19 7.716E-21 CHBr3
 210c 1.996E-21 6.036E-22 2.461E-22 3.240E-23 3.414E-25 0.000E+00 CHBr3
CHBr3
 300a 5.630E-18 4.299E-18 3.948E-18 3.744E-18 4.272E-18 4.535E-18 CHBr3
 300b 4.817E-18 5.227E-18 8.969E-19 9.049E-19 5.338E-19 1.676E-20 CHBr3
 300c 5.066E-21 1.783E-21 7.401E-22 9.748E-23 1.027E-24 0.000E+00 CHBr3
CH3I  |CH3I=>CH3+I     | CH3I = Methyl iodide    JPL10
 243a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH3I
 243b 3.958E-20 4.769E-20 8.257E-19 2.154E-19 7.349E-20 3.351E-20 CH3I
 243c 1.034E-20 4.435E-21 2.272E-21 4.393E-22 4.052E-24 0.000E+00 CH3I
CH3I
 300a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 CH3I
 300b 3.958E-20 4.769E-20 8.376E-19 2.438E-19 9.355E-20 4.680E-20 CH3I
 300c 1.529E-20 6.532E-21 3.328E-21 6.783E-22 1.038E-23 0.000E+00 CH3I
CF3I  |CF3I=>CF3+I     | CF3I = tri-fluoro iodo methane   JPL10
 243a 8.229E-21 3.885E-21 2.404E-21 1.653E-21 1.772E-21 2.856E-21 CF3I
 243b 4.178E-21 6.205E-21 5.540E-19 3.605E-19 2.108E-19 1.330E-19 CF3I
 243c 4.992E-20 2.036E-20 9.495E-21 1.567E-21 1.868E-23 0.000E+00 CF3I
CF3I
 300a 8.229E-21 3.885E-21 2.404E-21 1.653E-21 1.772E-21 2.856E-21 CF3I
 300b 4.178E-21 6.205E-21 5.164E-19 3.545E-19 2.275E-19 1.544E-19 CF3I
 300c 6.552E-20 2.972E-20 1.471E-20 2.620E-21 3.944E-23 0.000E+00 CF3I
OCS   |OCS=>CO+S       | OCS = carbonyl sulfide   JPL10
 200a 5.275E-20 3.879E-20 2.920E-20 2.343E-20 6.049E-20 1.232E-19 OCS
 200b 1.691E-19 2.181E-19 9.974E-21 4.126E-20 2.417E-20 9.292E-25 OCS
 200c 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 OCS
OCS
 300a 7.547E-20 5.314E-20 3.637E-20 2.436E-20 6.009E-20 1.222E-19 OCS
 300b 1.689E-19 2.186E-19 1.382E-20 4.616E-20 2.470E-20 3.294E-24 OCS
 300c 7.435E-26 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 OCS
PAN   |CH3C(O)COONO2=>  |PeroxyAcetylNitrate =CH3C(O)O2+NO2[0.70] =CH3C(O)O+NO3[0.30]
 250a 7.378E-19 1.680E-18 2.179E-18 3.774E-18 3.022E-18 2.163E-18 PAN
 250b 1.735E-18 1.343E-18 6.568E-20 9.393E-20 8.602E-20 2.421E-21 PAN
 250c 9.352E-22 4.320E-22 2.291E-22 5.393E-23 7.265E-25 0.000E+00 PAN
PAN   |
 298a 8.121E-19 1.847E-18 2.379E-18 4.129E-18 3.193E-18 2.239E-18 PAN
 298b 1.803E-18 1.407E-18 7.914E-20 1.055E-19 9.304E-20 3.531E-21 PAN
 298c 1.414E-21 6.696E-22 3.632E-22 9.109E-23 1.324E-24 0.000E+00 PAN
CH3NO3|CH3ONO2=>CH3O+NO2| Methyl nitrate JPL10
 200a 4.459E-18 8.856E-18 1.020E-17 1.021E-17 6.757E-18 3.480E-18 CH3NO3
 200b 2.248E-18 1.458E-18 2.364E-20 4.404E-20 6.296E-20 3.955E-21 CH3NO3
 200c 1.626E-21 6.610E-22 2.584E-22 2.194E-23 2.573E-27 0.000E+00 CH3NO3
CH3NO3
 300a 6.234E-18 1.238E-17 1.426E-17 1.427E-17 9.445E-18 4.866E-18 CH3NO3
 300b 3.143E-18 2.038E-18 3.219E-20 6.182E-20 8.858E-20 6.137E-21 CH3NO3
 300c 2.740E-21 1.236E-21 5.475E-22 6.702E-23 1.287E-26 0.000E+00 CH3NO3
ActAld|Acetaldhyde     |CH3CO=CH4+CO/CH3+HCO/H+CH3CO q=0.0/0.88/0.12 IUPAC14 P2 298K
p177a 0.000E+00 0.000E+00 1.989E-23 0.000E+00 3.699E-22 4.938E-22 ActAld
 177b 4.737E-22 4.659E-22 2.450E-20 3.409E-20 3.820E-20 3.732E-20 ActAld
 177c 2.707E-20 1.579E-20 6.566E-21 3.883E-22 5.683E-26 0.000E+00 ActAld
ActAld|
p566a 0.000E+00 0.000E+00 1.903E-23 0.000E+00 3.539E-22 4.725E-22 ActAld
 566b 4.533E-22 4.458E-22 2.270E-20 2.985E-20 3.199E-20 2.987E-20 ActAld
 566c 1.923E-20 9.497E-21 3.450E-21 1.914E-22 3.762E-26 0.000E+00 ActAld
ActAld|
p999a 0.000E+00 0.000E+00 1.822E-23 0.000E+00 3.389E-22 4.525E-22 ActAld
 999b 4.340E-22 4.269E-22 2.112E-20 2.647E-20 2.740E-20 2.479E-20 ActAld
 999c 1.485E-20 6.739E-21 2.319E-21 1.258E-22 2.790E-26 0.000E+00 ActAld
MeVK  |CH3C(O)CH=CH2 > | MethylVinyl Ketone = CH3C(O)CH=CH2    JPL10
p177a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MeVK
 177b 0.000E+00 0.000E+00 1.800E-22 4.760E-21 5.468E-21 5.834E-21 MeVK
 177c 5.243E-21 4.484E-21 3.669E-21 1.710E-21 9.063E-23 0.000E+00 MeVK
MeVK                   | =>C3H6+CO[0.6] CH2CHCO+CH3[0.2] CH3CO+C2H3[0.2]
p566a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MeVK
 566b 0.000E+00 0.000E+00 1.011E-22 2.673E-21 3.070E-21 3.275E-21 MeVK
 566c 2.943E-21 2.517E-21 2.061E-21 9.600E-22 5.079E-23 0.000E+00 MeVK
MeVK
p999a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MeVK
 999b 0.000E+00 0.000E+00 6.933E-23 1.833E-21 2.106E-21 2.247E-21 MeVK
 999c 2.019E-21 1.725E-21 1.414E-21 6.587E-22 3.477E-23 0.000E+00 MeVK
MeAcr |CH2C(CH3)CHO >  | Methacrolein => CH2=C(CH3)+HCO (q=0.003) JPL10
 298a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MeAcr
 298b 0.000E+00 0.000E+00 9.450E-24 2.852E-23 5.252E-23 7.912E-23 MeAcr
 298c 1.182E-22 1.500E-22 1.779E-22 1.959E-22 3.982E-23 0.000E+00 MeAcr
GlyAld|HOCH2CHO >      | Glycol Aldehyde => CH2OH+HCO[0.83] CH3OH+CO[0.10] OH+CH2CHO[0.07]   JPL10
 298a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 7.413E-20 1.879E-19 MeAcr
 298b 1.038E-19 4.946E-20 5.168E-20 5.719E-20 5.581E-20 4.810E-20 MeAcr
 298c 2.912E-20 1.567E-20 7.019E-21 7.099E-22 0.000E+00 0.000E+00 MeAcr
MEKeto|CH3COC2H5 >     | Methylethyl Ketone => C2H5+CH3CO[0.85] CH3+C2H5CO[0.15]  X67
p177a 0.000E+00 0.000E+00 4.387E-22 0.000E+00 4.393E-21 1.291E-21 MEKeto
 177b 1.231E-21 1.356E-21 3.133E-20 3.510E-20 3.397E-20 3.077E-20 MEKeto
 177c 1.981E-20 1.158E-20 5.697E-21 6.008E-22 2.756E-25 0.000E+00 MEKeto
MEKeto
p999a 0.000E+00 0.000E+00 1.982E-22 0.000E+00 1.984E-21 5.829E-22 MEKeto
 999b 5.559E-22 6.123E-22 1.415E-20 1.586E-20 1.534E-20 1.390E-20 MEKeto
 999c 8.947E-21 5.232E-21 2.574E-21 2.714E-22 1.244E-25 0.000E+00 MEKeto
PrAld |C2H5CHO >C2H5+  | Propionaldehyde(propanal) => C2H5+HCO  JPL10
 298a 0.000E+00 0.000E+00 1.797E-23 0.000E+00 3.430E-22 5.337E-22 PrAld
 298b 6.041E-22 6.842E-22 2.988E-20 4.520E-20 5.122E-20 5.545E-20 PrAld
 298c 4.628E-20 3.576E-20 2.436E-20 5.836E-21 1.246E-23 0.000E+00 PrAld
MGlyxl|CH3COC(O)H >HCO+| Methyl glyoxal = CH3COC(O)H => CH3CO + HCO   JPL10
p177a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MGlyxl
 177b 0.000E+00 0.000E+00 2.085E-20 3.955E-20 4.398E-20 4.414E-20 MGlyxl
 177c 3.504E-20 2.355E-20 1.811E-20 6.006E-21 1.256E-20 8.631E-22 MGlyxl
MGlyxl
p566a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MGlyxl
 566b 0.000E+00 0.000E+00 2.085E-20 3.955E-20 4.398E-20 4.414E-20 MGlyxl
 566c 3.504E-20 2.355E-20 1.811E-20 6.006E-21 7.045E-21 4.044E-22 MGlyxl
MGlyxl
p999a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 MGlyxl
 999b 0.000E+00 0.000E+00 2.085E-20 3.955E-20 4.398E-20 4.414E-20 MGlyxl
 999c 3.504E-20 2.355E-20 1.811E-20 6.006E-21 5.232E-21 2.543E-22 MGlyxl
Glyxla|CHOCHO=>HCO+HCO | Glyoxal[a] = CHOCHO => HCO+HCO      JPL10
p177a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Glyxla
 177b 0.000E+00 0.000E+00 1.173E-21 4.354E-21 5.353E-21 6.331E-21 Glyxla
 177c 7.090E-21 7.781E-21 7.452E-21 4.214E-21 5.124E-21 5.781E-23 Glyxla
Glyxla
p999a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Glyxla
 999b 0.000E+00 0.000E+00 1.173E-21 4.354E-21 5.353E-21 6.331E-21 Glyxla
 999c 7.090E-21 7.781E-21 7.452E-21 4.214E-21 2.864E-21 2.275E-23 Glyxla
Glyxlb|CHOCHO=>HCO+HCO | Glyoxal[b] = CHOCHO => H2+CO+CO     JPL10
p177a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Glyxlb
 177b 0.000E+00 0.000E+00 3.378E-21 1.177E-20 1.388E-20 1.453E-20 Glyxlb
 177c 1.224E-20 9.558E-21 6.758E-21 2.443E-21 7.973E-23 0.000E+00 Glyxlb
Glyxlb
p999a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Glyxlb
 999b 0.000E+00 0.000E+00 3.378E-21 1.177E-20 1.388E-20 1.453E-20 Glyxlb
 999c 1.224E-20 9.558E-21 6.758E-21 2.443E-21 7.973E-23 0.000E+00 Glyxlb
Glyxlc|CHOCHO=>HCO+HCO | Glyoxal[c] = CHOCHO => HCHO+CO      JPL10
p177a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Glyxlc
 177b 0.000E+00 0.000E+00 2.968E-21 1.178E-20 1.500E-20 1.704E-20 Glyxlc
 177c 1.636E-20 1.462E-20 1.148E-20 4.054E-21 4.054E-22 2.674E-24 Glyxlc
Glyxlc
p999a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Glyxlc
 999b 0.000E+00 0.000E+00 2.968E-21 1.178E-20 1.500E-20 1.704E-20 Glyxlc
 999c 1.636E-20 1.462E-20 1.148E-20 4.054E-21 2.775E-22 1.053E-24 Glyxlc
Acet-a|Acetn=CH3CO+CH3 | Acetone=CH3C(O)CH3          JPL10
p177a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Acet-a
 177b 0.000E+00 0.000E+00 0.000E+00 2.312E-20 2.824E-20 1.980E-20 Acet-a
 177c 5.927E-21 6.000E-22 5.868E-23 5.934E-25 0.000E+00 0.000E+00 Acet-a
Acet-a|
p566a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Acet-a
 566b 0.000E+00 0.000E+00 0.000E+00 1.486E-20 1.723E-20 1.240E-20 Acet-a
 566c 4.464E-21 7.146E-22 1.171E-22 2.202E-24 0.000E+00 0.000E+00 Acet-a
Acet-a|
p999a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Acet-a
 999b 0.000E+00 0.000E+00 0.000E+00 1.053E-20 1.237E-20 9.213E-21 Acet-a
 999c 3.702E-21 7.100E-22 1.357E-22 3.115E-24 0.000E+00 0.000E+00 Acet-a
Acet-b|Acetn=CH3+CH3+CO| Acetone=CH3C(O)CH3           JPL10
 235a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Acet-b
 235b 0.000E+00 0.000E+00 0.000E+00 3.678E-22 2.462E-22 1.158E-22 Acet-b
 235c 2.648E-23 6.014E-24 1.502E-24 4.211E-26 0.000E+00 0.000E+00 Acet-b
Acet-b|
 260a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Acet-b
 260b 0.000E+00 0.000E+00 0.000E+00 1.249E-21 1.020E-21 5.664E-22 Acet-b
 260c 1.681E-22 4.919E-23 1.477E-23 5.602E-25 0.000E+00 0.000E+00 Acet-b
Acet-b|
 298a 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 Acet-b
 298b 0.000E+00 0.000E+00 0.000E+00 4.209E-21 4.230E-21 2.804E-21 Acet-b
 298c 1.092E-21 4.079E-22 1.496E-22 7.707E-24 0.000E+00 0.000E+00 Acet-b
endofJ
------must have 'endofJ' to closeout the readin

Notes:
rev 7.3c (8/2015 = final version for Cloud-J v7.3c)
     new integrated solar fluxes and weighted X-sections for Rayleigh (only)
     in preparation for the 27 super-bins of Solar-J
     this should still reproduce Cloud-J v7.3 to <1%.
     not released ver 7.3b (6/2015)
     last FJ bin#18 cut at 778 nm to match RRTM, scaled Xsects by 2.131/1.805
     should be almost identical to results from 7.3

rev 7.3 (6/2014)
     initial dataset for Cloud-J v7.3 GMDD paper, revised for GMD paper to 7.3c
     needs v 7.2a code or later (Cloud-J)
     reformatted for unlimited read in (check dimension in read)
     long-name(A16) added to short-name(a6) plus notes
     each record is uniquly identified

rev 6.8d (6/2014)
    Acetaldehyde (CH3CO) fixed to account for Stern-Volmer q-yields (IUPAC P2 2013)

rev 6.8c (3/2013)
    Acetone major fixes - mistake with q-yields.
        NEW J-Acet-a (CH3O) is 3x (0km) to 5x (5km) faster than ver 6.8b
        NEW J-Acet-b (CO)   is 0.60x slower
        NEW in lower trop:  J-b / J-a = 0.28 (0km) to 0.18 (4km)

rev 6.8b (3/2012)
     Small fixes to correct short-w extrap.
     JPL 2010 rev 3/2012 VOC updates and change in Stern-Volmer method
        T is used to get p (or M) from the mean trop lapse rate
        thus VOCs are restricted to trop for accurate J's.
     Q-yields caclulated from Stern-Volmer relation at 3 tropospheric points.
        alt=   0 km      5 km      13 km
        M=   2.46E+19   1.50E+19   5.8E+18
        T=     295K      272K       220K
        p =    999 hPa   566 hPa    177 hPa
     X-sections can be interpolated as fn(T) or as fn(p) -
       thus each X-section block is identified by nnn(K) or pnnn(hPa)

==============================VOCs================================

PAN    = Peroxyacetyl nitrate = CH3C(O)COONO2
               CH3C(O)O2 + NO2   0.70   (Q fixed)
               CH3C(O)O + NO3    0.30

CH3NO3 = Methyl nitrate = CH3ONO2
               CH3O + NO2

ActAld = Acetaldehyde = CH3CHO      (IUPAC)
         Q-yield based on tables at 1 bar, only w > 300 nm
               CH4+CO     (1)  0.00    (Q fixed)
               CH3+HCO    (2)  0.88
               H+CH3CO    (3)  0.12

MeVK   = Methylvinyl ketone = CH3C(O)CH=CH2
         Q-yield = exp[-0.055*(w-308)]/5.5+9.2e-19*[M])
               C3H6+CO         0.60     (Q fixed)
               CH2CHCO+CH3     0.20
               CH3CO + C2H3    0.20

MeAcr  = Methacrolein CH2C(CH3)CHO
               CH2=C(CH3)+HCO  (recommended, uses q=0.003 everywhere)

GlyAld = Glycol aldehyde = HOCH2CHO
               CH2OH + HCO  (1)  0.83   (Q fixed)
               CH3OH + CO   (2)  0.10
               OH + CH2CHO  (3)  0.07

MEKeto = Methylethyl ketone = CH3COC2H5     (IUPAC)
               C2H5+CH3CO    0.85        (Q fixed)
               CH3+C2H5CO    0.15

PrAld  = Propionaldehyde (or propanal) = C2H5CHO
               C2H5 + HCO

MGlyxl = Methyl glyoxal = CH3COC(O)H
               CH3CO + HCO

Glyxl  = Glyoxal (CHO)2 or CHOCHO
               Glyxla   => HCO + HCO  (1) (Q by Xsects)
               Glyxlb   => H2 + 2 CO  (2)
               Glyxlc   => HCHO + CO  (3)

C3H6O = Acet = Acetone = CH3C(O)CH3
               Acet-a   => CH3CO+CH3     (Q by Xsects)
               Acet-b   => CH3+CH3+CO

===========================================================================

-------------------------other notes---------------------------------------
Solar fluxes from SUSIM:
11Nov1994 low solar
SOL#/cm2/s 1.360E+12 1.591E+12 1.629E+12 9.085E+11 7.674E+12 4.588E+12
           9.826E+12 1.209E+13 6.357E+14 4.040E+14 3.152E+14 5.897E+14
           7.705E+14 5.054E+14 8.934E+14 3.857E+15 1.544E+16 2.131E+17

std fast-JX = average of the two
SOL#/cm2/s 1.391E+12 1.627E+12 1.664E+12 9.278E+11 7.842E+12 4.680E+12
           9.918E+12 1.219E+13 6.364E+14 4.049E+14 3.150E+14 5.889E+14
           7.678E+14 5.045E+14 8.902E+14 3.853E+15 1.547E+16 2.131E+17

29Mar1992 med-high solar
SOL#/cm2/s 1.423E+12 1.662E+12 1.699E+12 9.468E+11 8.007E+12 4.771E+12
           1.001E+13 1.229E+13 6.370E+14 4.055E+14 3.148E+14 5.880E+14
           7.652E+14 5.034E+14 8.869E+14 3.849E+15 1.550E+16 2.131E+17

---------------------------------------------------------------------------
NO3 Xsections from JPL-2010:
   NO3a => NO2+O      (405 - 640 nm)  J_TOA = 0.2075 (190K)  0.1648 (298K)
   NO3b => NO+O2      (586 - 640 nm)  J_TOA = 0.0295 (190K)  0.0209 (298K)
     ratio = b/(a+b) = 0.1245 (190K)  0.1124 (298K)
recommend fixed Q-yield NO3b = 0.118,  NO3a = 0.882

NO3t 190   0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 5.296E-21 1.112E-18
NO3t 298   0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 3.796E-21 8.713E-19

NO3a   190 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 5.296E-21 9.736E-19
NO3a   298 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 3.796E-21 7.733E-19

NO3b   190 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 1.385E-19
NO3b   298 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00
           0.000E+00 0.000E+00 0.000E+00 0.000E+00 0.000E+00 9.797E-20

---------------------------------------------------------------------------
