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== feel free to experiment here ==
=== Species added ===


=== Table 1A - Bimolecular Ox ===
Species added between versions 14.5.0-alpha.5 and 14.5.0-alpha.9:


{| border=1 cellspacing=0 cellpadding=5  
{| border=1 cellspacing=0 cellpadding=5
|-valign="top" bgcolor="#CCCCCC"
!width='100px' bgcolor='#CCCCCC'|Name
!width="275px"|GEOS-Chem Reaction
!width='100px' bgcolor='#CCCCCC'|Formula
!width="275px"|v10 (JPL 10-6)
!width='200px' bgcolor='#CCCCCC'|Fullname
!width="275px"|JPL 15-10
!width='30px' bgcolor='#CCCCCC'|Advected
!width="275px"|Comparison
!width='30px' bgcolor='#CCCCCC'|Dry deposited
 
!width='30px' bgcolor='#CCCCCC'|Gas
|-valign="top"
!width='30px' bgcolor='#CCCCCC'|Photolyzed
|No quantitative updates || || ||
!width='30px' bgcolor='#CCCCCC'|Wet deposited


|-valign='top'
|ACO3
|C3H3O3
|Peroxyacetyl radical for APAN
|
|
|X
|
|
|-valign='top'
|ACR
|C3H4O
|Acrolein
|X
|X
|X
|X
|
|-valign='top'
|ACRO2
|C3H5O4
|Peroxy radical from ACR
|
|
|X
|
|
|-valign='top'
|ALK7
|C7H16
|Lumped >= C6 Alkanes
|X
|
|X
|
|
|-valign='top'
|APAN
|C3H3NO5
|Peroxyacryloyl nitrate
|X
|X
|X
|X
|X
|-valign='top'
|APINN
|C10H17NO4
|1st gen organic nitrate from APIN
|X
|X
|X
|X
|X
|-valign='top'
|APINO2
|C10H17O3
|Peroxy radical from APIN
|
|
|X
|
|
|-valign='top'
|APINP
|C10H18O3
|Hydroperoxide from APIN
|X
|X
|X
|
|X
|-valign='top'
|AROMCHO
|C5H6O4
|ACCOMECHO from MCM
|X
|X
|X
|
|X
|-valign='top'
|AROMCO3
|C5H5O6
|Lumped aromatic peroxyacetyl radical
|
|
|X
|
|
|-valign='top'
|AROMPN
|C5H5NO8
|Lumped PN from aromatics
|X
|X
|X
|X
|X
|-valign='top'
|BPINN
|C10H17NO4
|Saturated 1st gen BPIN organic nitrate
|X
|X
|X
|X
|X
|-valign='top'
|BPINO
|C9H14O
|Ketone from BPIN
|X
|X
|X
|
|X
|-valign='top'
|BPINO2
|C10H17O3
|Peroxy radical from BPIN
|
|
|X
|
|
|-valign='top'
|BPINON
|C9H13NO4
|Saturated 2nd gen BPIN organic nitrate
|X
|X
|X
|X
|X
|-valign='top'
|BPINOO2
|C10H17O3
|2nd-gen peroxy radical from BPIN
|
|
|X
|
|
|-valign='top'
|BPINOOH
|C9H14O3
|2nd-gen peroxide from BPIN
|X
|X
|X
|
|X
|-valign='top'
|BPINP
|C10H18O3
|Peroxide from BPIN
|X
|X
|X
|
|X
|-valign='top'
|BUTN
|C4H7NO4
|C4H6 alkyl nitrate
|X
|X
|X
|
|X
|-valign='top'
|BUTO2
|C4H7O3
|peroxy radical from C4H6
|
|
|X
|
|
|-valign='top'
|C4H6
|C4H6
|1,3-butadiene
|X
|
|X
|
|
|-valign='top'
|C96N
|C9H15NO4
|Saturated 2nd gen monoterpene organic nitrate
|X
|X
|X
|X
|X
|-valign='top'
|C96O2
|C10H17O3
|2nd-gen peroxy radical from APIN
|
|
|X
|
|
|-valign='top'
|C96O2H
|C9H16O3
|Peroxide from APIN 2nd gen
|X
|X
|X
|
|X
|-valign='top'
|EBZ
|C8H10
|Ethylbenzene
|X
|
|X
|
|
|-valign='top'
|GCO3
|HOCH2CO3
|Peroxyacetyl radical for PHAN
|
|
|X
|
|
|-valign='top'
|HACTA
|HOCH2CO2H
|Hydroxyacetic/glycolic acid
|X
|X
|X
|
|X
|-valign='top'
|LIMAL
|C10H16O2
|Aldehyde from limonene
|X
|X
|X
|
|X
|-valign='top'
|LIMKB
|C10H16O3
|2nd gen ketone from limonene
|X
|X
|X
|
|X
|-valign='top'
|LIMKET
|C10H16O2
|Ketone from limonene
|X
|X
|X
|
|X
|-valign='top'
|LIMKO2
|C10H17O3
|2nd-gen peroxy radical from LIMO
|
|
|X
|
|
|-valign='top'
|LIMN
|C10H17NO4
|Saturated 1st gen limonene organic nitrate
|X
|X
|X
|X
|X
|-valign='top'
|LIMNB
|C10H15NO4
|Saturated 1st gen LIMO organic nitrate
|X
|X
|X
|X
|X
|-valign='top'
|LIMO2H
|C10H18O3
|Acid from LIMO
|X
|X
|X
|
|X
|-valign='top'
|LIMO3
|C10H17O3
|Acylperoxy radical from LIMO
|
|
|X
|
|
|-valign='top'
|LIMO3H
|C10H18O4
|Peracid from LIMO
|X
|X
|X
|
|X
|-valign='top'
|LIMPAN
|C10H17NO4
|PAN from LIMO
|X
|X
|X
|X
|X
|-valign='top'
|MEKCO3
|C3H5O4
|False
|
|
|X
|
|
|-valign='top'
|MEKPN
|C3H5NO6
|MEK peroxyacetyl nitrate
|X
|X
|X
|X
|X
|-valign='top'
|MYRCO
|C10H18O3
|Aldehyde or ketone from myrcene
|X
|X
|X
|
|X
|-valign='top'
|PHAN
|C2H3NO6
|Peroxyhydroxyacetic nitric anhydride
|X
|X
|X
|X
|X
|-valign='top'
|PIN
|C10H17NO4
|Saturated 1st gen monoterpene organic nitrate
|X
|X
|X
|X
|X
|-valign='top'
|PINAL
|C10H16O2
|Pinonaldehyde
|X
|X
|X
|
|X
|-valign='top'
|PINO3
|C10H17O3
|Acylperoxy radical from APIN
|
|
|X
|
|
|-valign='top'
|PINO3H
|C10H18O4
|Pinonic peracid
|X
|X
|X
|
|X
|-valign='top'
|PINONIC
|C10H18O3
|Pinonic acid
|X
|X
|X
|
|X
|-valign='top'
|PINPAN
|C10H17NO4
|PAN from pinonaldehyde
|X
|X
|X
|X
|X
|-valign='top'
|R7N1
|C7H15NO5
|Peroxy radical from R7N2
|
|
|X
|
|
|-valign='top'
|R7N2
|RO2NO
|C7 Lumped alkyl nitrate
|X
|X
|X
|X
|X
|-valign='top'
|R7O2
|C7H15O2
|Peroxy radical from ALK7
|
|
|X
|
|
|-valign='top'
|R7P
|C7H16O2
|Peroxide from R7O2
|X
|X
|X
|X
|X
|-valign='top'
|RNO3
|RO2NO
|Lumped aromatic nitrate
|X
|X
|X
|X
|X
|-valign='top'
|STYR
|C8H8
|Styrene
|X
|
|X
|
|
|-valign='top'
|TLFUO2
|C5H7O5
|False
|
|
|X
|
|
|-valign='top'
|TLFUONE
|C5H6O2
|Aromatic furanones
|X
|X
|X
|
|X
|-valign='top'
|TMB
|C8H10
|Trimethylbenzenes
|
|
|X
|
|
|-valign='top'
|ZRO2
|C7H9O5
|RO2 for making lumped aromatic nitrate
|
|
|X
|
|
|}
|}


=== Table 1A - Bimolecular O1D ===
 
=== Species removed===
{| border=1 cellspacing=0 cellpadding=5
|-valign="top" bgcolor="#CCCCCC"
!width="275px"|GEOS-Chem Reaction
!width="275px"|v10 (JPL 10-6)
!width="275px"|JPL 15-10
!width="275px"|Comparison
 
|-valign="top"
|CH3Cl + O1D || not active || || 
 
|-valign="top"
|CH3CCl3 + O1D || not active || ||
 
|-valign="top"
|O1D + HCFC22 = O + HCFC22 + ClO + Cl
|1e-10
|1.02e-10
|[[File:JPL201510andGCv10_O1DplHCFC22_eq_OplHCFC22plClOplCl.png|200px|thumb|left|JPL201510andGCv10_O1DplHCFC22_eq_OplHCFC22plClOplCl.png]]
 
|-valign="top"
|O1D + HCFC142b
|2.20E-10
|2.00E-10
|[[File:JPL201510andGCv10_O1DplHCFC142b.png|200px|thumb|left|JPL201510andGCv10_O1DplHCFC142b.png]]


|-valign="top"
Species removed between versions 14.5.0-alpha.5 and 14.5.0-alpha.9:
|O1D + CFC113
|2.00E-10
|2.32E-10
|[[File:JPL201510andGCv10_O1DplCFC113.png|200px|thumb|left|JPL201510andGCv10_O1DplCFC113.png]]


|-valign="top"
{| border=1 cellspacing=0 cellpadding=5
|O1D + CFC114
!width='100px' bgcolor='#CCCCCC'|Name
|1.30E-10
!width='100px' bgcolor='#CCCCCC'|Formula
|1.3E-10*exp(-25/T)
!width='200px' bgcolor='#CCCCCC'|Fullname
|[[File:JPL201510andGCv10_O1DplCFC114.png|200px|thumb|left|JPL201510andGCv10_O1DplCFC114.png]]
!width='30px' bgcolor='#CCCCCC'|Advected
 
!width='30px' bgcolor='#CCCCCC'|Dry deposited
|-valign="top"
!width='30px' bgcolor='#CCCCCC'|Gas
|O1D + CFC115
!width='30px' bgcolor='#CCCCCC'|Photolyzed
|5.0E-11
!width='30px' bgcolor='#CCCCCC'|Wet deposited
|5.4E-11*exp(-30/T)
|[[File:JPL201510andGCv10_O1DplCFC115.png|200px|thumb|left|JPL201510andGCv10_O1DplCFC115.png]]


|}
|}
<table>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 1A - Bimolecular Singlet O2 </th></tr>
<tr><td colspan=4>No quantitative updates.</td></tr>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 1B - Bimolecular HOx </th></tr>
<tr><td colspan=4>No quantitative updates.</td></tr>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 1C - Bimolecular  NOx  </th></tr>
<tr><td colspan=4>No quantitative updates.</td></tr>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 1D - Bimolecular Organic</th></tr>
<tr><th width="20%">GEOS-Chem Reaction</th><th>v10 (JPL 10-6)</th><th>JPL 15-10</th><th>Comparison</th></tr>
<tr><td>MACR + O3 = OH + HO2 + HCOOH + CO + MGLY + CH2O</td><td>1.40E-15*exp(-2100/T)</td><td>1.5e-15*exp(-2110/T)</td><td width="30%">[[File:JPL201510andGCv10_MACRplO3_eq_OHplHO2plHCOOHplCOplMGLYplCH2O.png|200px|thumb|left|JPL201510andGCv10_MACRplO3_eq_OHplHO2plHCOOHplCOplMGLYplCH2O.png]]</td></tr>
<tr><td>MVK + O3 = OH + HO2 + HCOOH + CO + ALD2 + MGLY + CH2O</td><td>8.50E-16*exp(-1520/T)</td><td>8.5e-16*exp(-1520/T)</td><td width="30%">[[File:JPL201510andGCv10_MVKplO3_eq_OHplHO2plHCOOHplCOplALD2plMGLYplCH2O.png|200px|thumb|left|JPL201510andGCv10_MVKplO3_eq_OHplHO2plHCOOHplCOplALD2plMGLYplCH2O.png]]</td></tr>
<tr><td>MACR + OH = MAO3 + MRO2</td><td>8.0E-12*exp(380/T)</td><td>9.6e-12*exp(360./T)</td><td width="30%">[[File:JPL201510andGCv10_MACRplOH_eq_MAO3plMRO2.png|200px|thumb|left|JPL201510andGCv10_MACRplOH_eq_MAO3plMRO2.png]]</td></tr>
<tr><td>MVK + OH = VRO2</td><td>2.6e-12*exp(610/T)</td><td>2.7e-12*exp(580./T)</td><td width="30%">[[File:JPL201510andGCv10_MVKplOH_eq_VRO2.png|200px|thumb|left|JPL201510andGCv10_MVKplOH_eq_VRO2.png]]</td></tr>
<tr><td>ISOP + OH = RIO2</td><td>3.1e-11*exp(350/T)</td><td>3.0e-11*exp(360./T)</td><td width="30%">[[File:JPL201510andGCv10_ISOPplOH_eq_RIO2.png|200px|thumb|left|JPL201510andGCv10_ISOPplOH_eq_RIO2.png]]</td></tr>
<tr><td>MACR + NO3 = MAN2</td><td>2.30e-15</td><td>3.4e-15</td><td width="30%">[[File:JPL201510andGCv10_MACRplNO3_eq_MAN2.png|200px|thumb|left|JPL201510andGCv10_MACRplNO3_eq_MAN2.png]]</td></tr>
<tr><td>ISOP + NO3 = INO2</td><td>3.3E-12*exp(-450/T)</td><td>3.5e-12*exp(-450/T)</td><td width="30%">[[File:JPL201510andGCv10_ISOPplNO3_eq_INO2.png|200px|thumb|left|JPL201510andGCv10_ISOPplNO3_eq_INO2.png]]</td></tr>
<tr><th colspan=4>Table 1F - Bimolecular ClOx </th></tr>
<tr><td colspan=4>Non CFC/HCFC ClOx needs review.  (volunteer by putting your name here)</td></tr>
<tr><td>OH + HCFC22 = Cl + H2O</td><td>1.05E-12*exp(-1600./T)</td><td>9.2e-13*exp(-1560./T)</td><td width="30%">[[File:JPL201510andGCv10_OHplHCFC22_eq_ClplH2O.png|200px|thumb|left|JPL201510andGCv10_OHplHCFC22_eq_ClplH2O.png]]</td></tr>
<tr><td>OH + HCFC123 = Cl + H2O</td><td>6.30E-13*exp(-850./T)</td><td>7.4e-13*exp(-900./T)</td><td width="30%">[[File:JPL201510andGCv10_OHplHCFC123_eq_ClplH2O.png|200px|thumb|left|JPL201510andGCv10_OHplHCFC123_eq_ClplH2O.png]]</td></tr>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 1G - Bimolecular BrOx </th></tr>
<tr><td colspan=4>Needs review. (volunteer by putting your name here)</td></tr>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 1H - Bimolecular IOx </th></tr>
<tr><td colspan=4>Needs review. (volunteer by putting your name here)</td></tr>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 1I - Bimolecular SOx </th></tr>
<tr><td colspan=4>Needs review. (volunteer by putting your name here)</td></tr>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 2-1 - Termolecular</th></tr>
<tr><th width="20%">GEOS-Chem Reaction</th><th>v10 (JPL 10-6)</th><th>JPL 15-10</th><th>Comparison</th></tr>
<tr><td>HO2 + NO2 + M = HNO4</td><td>GP(A0 = 2.e-31, B0 = 3.4, A1 = 2.9e-12, B1 = 1.1)</td><td>GP(A0 = 1.9e-31, B0 = 3.4, A1 = 4e-12, B1 = 0.3)</td><td width="30%">[[File:JPL201510andGCv10_HO2plNO2plM_eq_HNO4.png|200px|thumb|left|JPL201510andGCv10_HO2plNO2plM_eq_HNO4.png]]</td></tr>
<tr><td>NO2 + NO3 + M = N2O5</td><td>GP(A0 = 2.00E-30, B0 = 4.4E+00, A1 = 1.40E-12, B1 = 7.0E-01)</td><td>GP(A0 = 2.4e-30, B0 = 3., A1 = 1.6e-12, B1 = -0.1)</td><td width="30%">[[File:JPL201510andGCv10_NO2plNO3plM_eq_N2O5.png|200px|thumb|left|JPL201510andGCv10_NO2plNO3plM_eq_N2O5.png]]</td></tr>
<tr><td>OH + CO + M = H + CO2</td><td>GY(A0 = 5.9e-33, B0 = 1.4e0, A1 = 1.1e-12, B1 = -1.3e0, A2 = 1.5e-13, B2 = -0.6e0, A3 = 2.1e09, B3 = -6.1e0)</td><td>GY(A0 = 5.9e-33, B0 = 1., A1 = 1.1e-12, B1 = -1.3e0, A2 = 1.5e-13, B2 = 0., A3 = 2.1e09, B3 = -6.1e0)</td><td width="30%">[[File:JPL201510andGCv10_OHplCOplM_eq_HplCO2.png|200px|thumb|left|JPL201510andGCv10_OHplCOplM_eq_HplCO2.png]]</td></tr>
<tr><td>OH + PRPE + M = PO2</td><td>GP(A0 = 8.00E-27, B0 = 3.5E+00, A1 = 3.00E-11, B1 = 1.0E+00)</td><td>GP(A0 = 4.6e-27, B0 = 4., A1 = 2.6e-11, B1 = 1.3)</td><td width="30%">[[File:JPL201510andGCv10_OHplPRPEplM_eq_PO2.png|200px|thumb|left|JPL201510andGCv10_OHplPRPEplM_eq_PO2.png]]</td></tr>
<tr><td>ClO + ClO + M = Cl2O2</td><td>GP(1.60E-32, 4.5E+00 , 3.00E-12, 2.0E+00)</td><td>GP(A0 = 1.9e-32, B0 = 3.6, A1 = 3.7e-12, B1 = 1.6)</td><td width="30%">[[File:JPL201510andGCv10_ClOplClOplM_eq_Cl2O2.png|200px|thumb|left|JPL201510andGCv10_ClOplClOplM_eq_Cl2O2.png]]</td></tr>
<tr><th colspan=4 bgcolor="#CCFFFF">Table 3-1</th></tr>
<tr><td>N2O5 = NO2 + NO3</td><td>GP(A0 = 7.40E-04, B0 = 4.4E+00, C0 = -11000., A1 = 5.18E+14, B1 = 7.0E-01, C1 = -11000.)</td><td>GP(A0 = 2.4e-30/5.8e-27, B0 = 3., C0 = -10840, A1 = 1.6e-12/5.8e-27, B1 = -0.1, C1 = -10840)</td><td width="30%">[[File:JPL201510andGCv10_N2O5_eq_NO2plNO3.png|200px|thumb|left|JPL201510andGCv10_N2O5_eq_NO2plNO3.png]]</td></tr>
<tr><td>HNO4 = HO2 + NO2</td><td>GP(A0 = 2.e-31 / 2.1e-27, B0 = 3.4, C0 = -10900., A1 = 2.9e-12 / 2.1e-27, B1 = 1.1, C1 = -10900.)</td><td>GP(A0 = 1.9e-31 / 2.1e-27, B0 = 3.4, C0 = -10900., A1 = 4e-12 / 2.1e-27, B1 = 0.3, C1 = -10900.)</td><td width="30%">[[File:JPL201510andGCv10_HNO4_eq_HO2plNO2.png|200px|thumb|left|JPL201510andGCv10_HNO4_eq_HO2plNO2.png]]</td></tr>
<tr><td colspan=4>1. Termolecular rates coefficients are evaluated from -0.5km to 11km in the  1976 US Std Atmosphere temperature and pressures</td></tr>
<tr><td colspan=4>2. GP is short hand for the GEOS-Chem rate form denoted by P in globchem.dat and corresponding to the JPL termolecular rate defined as k_f([M],T) in Section 2.1</td></tr>
<tr><td colspan=4>3. GY is short hand for the GEOS-Chem rate form denoted by Y in globchem.dat and corresponding to the JPL termolecular rate defined as k^{ca}_f([M],T) in Section 2.1</td></tr>
</table>
--[[User:Bmy|Bob Y.]] ([[User talk:Bmy|talk]]) 19:54, 19 May 2015 (UTC)

Latest revision as of 19:10, 3 October 2024

Species added

Species added between versions 14.5.0-alpha.5 and 14.5.0-alpha.9:

Name Formula Fullname Advected Dry deposited Gas Photolyzed Wet deposited
ACO3 C3H3O3 Peroxyacetyl radical for APAN X
ACR C3H4O Acrolein X X X X
ACRO2 C3H5O4 Peroxy radical from ACR X
ALK7 C7H16 Lumped >= C6 Alkanes X X
APAN C3H3NO5 Peroxyacryloyl nitrate X X X X X
APINN C10H17NO4 1st gen organic nitrate from APIN X X X X X
APINO2 C10H17O3 Peroxy radical from APIN X
APINP C10H18O3 Hydroperoxide from APIN X X X X
AROMCHO C5H6O4 ACCOMECHO from MCM X X X X
AROMCO3 C5H5O6 Lumped aromatic peroxyacetyl radical X
AROMPN C5H5NO8 Lumped PN from aromatics X X X X X
BPINN C10H17NO4 Saturated 1st gen BPIN organic nitrate X X X X X
BPINO C9H14O Ketone from BPIN X X X X
BPINO2 C10H17O3 Peroxy radical from BPIN X
BPINON C9H13NO4 Saturated 2nd gen BPIN organic nitrate X X X X X
BPINOO2 C10H17O3 2nd-gen peroxy radical from BPIN X
BPINOOH C9H14O3 2nd-gen peroxide from BPIN X X X X
BPINP C10H18O3 Peroxide from BPIN X X X X
BUTN C4H7NO4 C4H6 alkyl nitrate X X X X
BUTO2 C4H7O3 peroxy radical from C4H6 X
C4H6 C4H6 1,3-butadiene X X
C96N C9H15NO4 Saturated 2nd gen monoterpene organic nitrate X X X X X
C96O2 C10H17O3 2nd-gen peroxy radical from APIN X
C96O2H C9H16O3 Peroxide from APIN 2nd gen X X X X
EBZ C8H10 Ethylbenzene X X
GCO3 HOCH2CO3 Peroxyacetyl radical for PHAN X
HACTA HOCH2CO2H Hydroxyacetic/glycolic acid X X X X
LIMAL C10H16O2 Aldehyde from limonene X X X X
LIMKB C10H16O3 2nd gen ketone from limonene X X X X
LIMKET C10H16O2 Ketone from limonene X X X X
LIMKO2 C10H17O3 2nd-gen peroxy radical from LIMO X
LIMN C10H17NO4 Saturated 1st gen limonene organic nitrate X X X X X
LIMNB C10H15NO4 Saturated 1st gen LIMO organic nitrate X X X X X
LIMO2H C10H18O3 Acid from LIMO X X X X
LIMO3 C10H17O3 Acylperoxy radical from LIMO X
LIMO3H C10H18O4 Peracid from LIMO X X X X
LIMPAN C10H17NO4 PAN from LIMO X X X X X
MEKCO3 C3H5O4 False X
MEKPN C3H5NO6 MEK peroxyacetyl nitrate X X X X X
MYRCO C10H18O3 Aldehyde or ketone from myrcene X X X X
PHAN C2H3NO6 Peroxyhydroxyacetic nitric anhydride X X X X X
PIN C10H17NO4 Saturated 1st gen monoterpene organic nitrate X X X X X
PINAL C10H16O2 Pinonaldehyde X X X X
PINO3 C10H17O3 Acylperoxy radical from APIN X
PINO3H C10H18O4 Pinonic peracid X X X X
PINONIC C10H18O3 Pinonic acid X X X X
PINPAN C10H17NO4 PAN from pinonaldehyde X X X X X
R7N1 C7H15NO5 Peroxy radical from R7N2 X
R7N2 RO2NO C7 Lumped alkyl nitrate X X X X X
R7O2 C7H15O2 Peroxy radical from ALK7 X
R7P C7H16O2 Peroxide from R7O2 X X X X X
RNO3 RO2NO Lumped aromatic nitrate X X X X X
STYR C8H8 Styrene X X
TLFUO2 C5H7O5 False X
TLFUONE C5H6O2 Aromatic furanones X X X X
TMB C8H10 Trimethylbenzenes X
ZRO2 C7H9O5 RO2 for making lumped aromatic nitrate X


Species removed

Species removed between versions 14.5.0-alpha.5 and 14.5.0-alpha.9:

Name Formula Fullname Advected Dry deposited Gas Photolyzed Wet deposited
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