TY - JOUR
T1 - The stable isotopic composition of molecular hydrogen in the tropopause region probed by the CARIBIC aircraft
AU - Batenburg, A.M.
AU - Schuck, T.J.
AU - Baker, A.K.
AU - Zahn, A.
AU - Brenninkmeijer, C.A.M.
AU - Röckmann, T.
PY - 2012
Y1 - 2012
N2 - More than 450 air samples that were collected in the upper troposphere – lower stratosphere
(UTLS) region around the tropopause (TP) by the CARIBIC aircraft (Civil Aircraft
for the Regular Investigation of the Atmosphere Based on an Instrument Container)
have been analyzed 5 for molecular hydrogen (H2) mixing ratios (m(H2)) and H2
isotopic composition (deuterium content, D).
More than 120 of the analysed samples consisted of air from the lowermost stratosphere
(LMS). These show that m(H2) does not vary appreciably with O3-derived
height above the thermal TP, whereas D does increase with height. The isotope
10 enrichment is caused by competing H2 production and destruction processes that enrich
the stratospheric H2 reservoir in deuterium (D); the exact shapes of the profiles
are mainly determined by mixing of stratospheric with tropospheric air. Tight negative
correlations are found between D and the mixing ratios of methane (CH4)
and nitrous oxide (N2O), as a result of the relatively long lifetimes of these three
15 species. The correlations are described by D [h] = −0.35 ·m(CH4)[ppb]+768 and
D [h] = −1.90·m(N2O)[ppb]+745. These correlations are similar to previously published
results and likely hold globally.
Samples that were collected from the Indian subcontinent up to 40 N before, during
and after the summer monsoon season show no significant seasonal change in m(H2),
20 but D is up to 15h lower in the July, August and September monsoon samples.
This D lowering is correlated with m(CH4) increase. The significant correlation with
m(CH4) and the absence of a perceptible m(H2) increase that accompanies the D
lowering indicates that microbial production of very D-depleted H2 in the wet season
may contribute to this phenomenon.
25 Some of the samples have very high m(H2) and very low D values, which indicates
a pollution effect. Aircraft engine exhaust plumes are a suspected cause, since the
effect mostly occurs in samples collected close to airports, but no similar signals are
found in other chemical tracers to support this. The isotopic source signature of the H2 pollution seems to be on the low end of the signature for fossil fuel burning.
AB - More than 450 air samples that were collected in the upper troposphere – lower stratosphere
(UTLS) region around the tropopause (TP) by the CARIBIC aircraft (Civil Aircraft
for the Regular Investigation of the Atmosphere Based on an Instrument Container)
have been analyzed 5 for molecular hydrogen (H2) mixing ratios (m(H2)) and H2
isotopic composition (deuterium content, D).
More than 120 of the analysed samples consisted of air from the lowermost stratosphere
(LMS). These show that m(H2) does not vary appreciably with O3-derived
height above the thermal TP, whereas D does increase with height. The isotope
10 enrichment is caused by competing H2 production and destruction processes that enrich
the stratospheric H2 reservoir in deuterium (D); the exact shapes of the profiles
are mainly determined by mixing of stratospheric with tropospheric air. Tight negative
correlations are found between D and the mixing ratios of methane (CH4)
and nitrous oxide (N2O), as a result of the relatively long lifetimes of these three
15 species. The correlations are described by D [h] = −0.35 ·m(CH4)[ppb]+768 and
D [h] = −1.90·m(N2O)[ppb]+745. These correlations are similar to previously published
results and likely hold globally.
Samples that were collected from the Indian subcontinent up to 40 N before, during
and after the summer monsoon season show no significant seasonal change in m(H2),
20 but D is up to 15h lower in the July, August and September monsoon samples.
This D lowering is correlated with m(CH4) increase. The significant correlation with
m(CH4) and the absence of a perceptible m(H2) increase that accompanies the D
lowering indicates that microbial production of very D-depleted H2 in the wet season
may contribute to this phenomenon.
25 Some of the samples have very high m(H2) and very low D values, which indicates
a pollution effect. Aircraft engine exhaust plumes are a suspected cause, since the
effect mostly occurs in samples collected close to airports, but no similar signals are
found in other chemical tracers to support this. The isotopic source signature of the H2 pollution seems to be on the low end of the signature for fossil fuel burning.
U2 - 10.5194/acpd-12-589-2012
DO - 10.5194/acpd-12-589-2012
M3 - Article
SN - 1680-7375
VL - 12
SP - 589
EP - 622
JO - Atmospheric Chemistry and Physics Discussions
JF - Atmospheric Chemistry and Physics Discussions
ER -