TY - JOUR
T1 - The stable isotopic signature of biologically produced molecular hydrogen (H2)
AU - Walter, S.
AU - Laukenmann, S.
AU - Stams, A.J.M.
AU - Vollmer, M.K.
AU - Gleixner, G.
AU - Roeckmann, T.
PY - 2011
Y1 - 2011
N2 - Biologically produced molecular hydrogen (H2) is characterized by a very strong depletion
in deuterium. Although the biological source to the atmosphere is small compared
to photochemical or combustion sources, it makes an important contribution to
the global isotope budget of molecular hydrogen (H2). Large uncertainties exist in the
quantification of the individual production and degradation processes that contribute to
the atmospheric budget, and isotope measurements are a tool to distinguish the contributions
from the different sources. Measurements of δD from the various H2 sources
are scarce and for biologically produced H2 only very few measurements exist. Here
the first systematic study of the isotopic composition of biologically produced H2 is
presented.
We investigated δD of H2 produced in a biogas plant, covering different treatments
of biogas production, and from several H2 producing microorganisms such as bacteria
or green algae. A Keeling plot analysis provides a robust overall source sig
nature of δD = –712‰ (±13‰) for the samples from the biogas reactor (at 38 °C,
δDH2O = 73.4 ‰), with a fractionation constant εH2−H2O of –689‰ (±20 ‰). The pure
culture samples from different microorganisms give a mean source signature of δD =
–728‰ (± 39 ‰), and a fractionation constant εH2−H2O of –711‰ (± 45 ‰) between
H2 and the water, respectively. The results confirm the massive deuterium depletion
of biologically produced H2 as was predicted by calculation of the thermodynamic fractionation
factors for hydrogen exchange between H2 and water vapor. As expected
for a thermodynamic equilibrium, the fractionation factor is largely independent of the
substrates used and the H2 production conditions. The predicted equilibrium fractionation
coefficient is positively correlated with temperature and we measured a change
25 of 2.2‰/°C between 45 °C and 60 °C. This is in general agreement with the theoretical predictions.
AB - Biologically produced molecular hydrogen (H2) is characterized by a very strong depletion
in deuterium. Although the biological source to the atmosphere is small compared
to photochemical or combustion sources, it makes an important contribution to
the global isotope budget of molecular hydrogen (H2). Large uncertainties exist in the
quantification of the individual production and degradation processes that contribute to
the atmospheric budget, and isotope measurements are a tool to distinguish the contributions
from the different sources. Measurements of δD from the various H2 sources
are scarce and for biologically produced H2 only very few measurements exist. Here
the first systematic study of the isotopic composition of biologically produced H2 is
presented.
We investigated δD of H2 produced in a biogas plant, covering different treatments
of biogas production, and from several H2 producing microorganisms such as bacteria
or green algae. A Keeling plot analysis provides a robust overall source sig
nature of δD = –712‰ (±13‰) for the samples from the biogas reactor (at 38 °C,
δDH2O = 73.4 ‰), with a fractionation constant εH2−H2O of –689‰ (±20 ‰). The pure
culture samples from different microorganisms give a mean source signature of δD =
–728‰ (± 39 ‰), and a fractionation constant εH2−H2O of –711‰ (± 45 ‰) between
H2 and the water, respectively. The results confirm the massive deuterium depletion
of biologically produced H2 as was predicted by calculation of the thermodynamic fractionation
factors for hydrogen exchange between H2 and water vapor. As expected
for a thermodynamic equilibrium, the fractionation factor is largely independent of the
substrates used and the H2 production conditions. The predicted equilibrium fractionation
coefficient is positively correlated with temperature and we measured a change
25 of 2.2‰/°C between 45 °C and 60 °C. This is in general agreement with the theoretical predictions.
U2 - 10.5194/bg-9-4115-2012
DO - 10.5194/bg-9-4115-2012
M3 - Article
SN - 1810-6277
VL - 9
SP - 12521
EP - 12541
JO - Biogeosciences Discussions
JF - Biogeosciences Discussions
ER -