A gas chromatography/pyrolysis/isotope ratio mass spectrometry system for high-precision deltaD measurements of atmospheric methane extracted from ice cores.

Air enclosures in polar ice cores represent the only direct paleoatmospheric archive. Analysis of the entrapped air provides clues to the climate system of the past in decadal to centennial resolution. A wealth of information has been gained from measurements of concentrations of greenhouse gases; however, little is known about their isotopic composition. In particular, stable isotopologues (deltaD and delta(13)C) of methane (CH(4)) record valuable information on its global cycle as the different sources exhibit distinct carbon and hydrogen isotopic composition. However, CH(4) isotope analysis is limited by the large sample size required and the demanding analysis as high precision is required. Here we present a highly automated, high-precision online gas chromatography/pyrolysis/isotope ratio monitoring mass spectrometry (GC/P/irmMS) technique for the analysis of deltaD(CH(4)). It includes gas extraction from ice, preconcentration, gas chromatographic separation and pyrolysis of CH(4) from roughly 500 g of ice with CH(4) concentrations as low as 350 ppbv. Ice samples with approximately 40 mL air and only approximately 1 nmol CH(4) can be measured with a precision of 3.4 per thousand. The precision for 65 mL air samples with recent atmospheric concentration is 1.5 per thousand. The CH(4) concentration can be obtained along with isotope data which is crucial for reporting ice core data on matched time scales and enables us to detect flaws in the measurement procedure. Custom-made script-based processing of MS raw and peak data enhance the system's performance with respect to stability, peak size dependency, hence precision and accuracy and last but not least time requirement.

[1]  T. Sowers Atmospheric methane isotope records covering the Holocene period , 2010 .

[2]  W. Brand,et al.  The stable isotope signature of methane emitted from plant material under UV irradiation , 2009 .

[3]  Quan Hua,et al.  14CH4 Measurements in Greenland Ice: Investigating Last Glacial Termination CH4 Sources , 2009, Science.

[4]  A. Sessions,et al.  Memory effects in compound-specific D/H analysis by gas chromatography/pyrolysis/isotope-ratio mass spectrometry. , 2008, Analytical chemistry.

[5]  J. Schmitt,et al.  A gas chromatography/combustion/isotope ratio mass spectrometry system for high-precision delta13C measurements of atmospheric methane extracted from ice core samples. , 2008, Rapid communications in mass spectrometry : RCM.

[6]  T. Stocker,et al.  Orbital and millennial-scale features of atmospheric CH4 over the past 800,000 years , 2008, Nature.

[7]  J. Schmitt,et al.  Changing boreal methane sources and constant biomass burning during the last termination , 2008, Nature.

[8]  H. Oerter,et al.  Accumulation and stable-isotope content in the hinterland of Neumayer station, Antarctica, since the IPY 1957/58. , 2008 .

[9]  H. Schaefer,et al.  Measurement of stable carbon isotope ratios of methane in ice samples , 2007 .

[10]  V. Petrenko,et al.  Ice Record of δ13C for Atmospheric CH4 Across the Younger Dryas-Preboreal Transition , 2006, Science.

[11]  D. Hauglustaine,et al.  Role of methane and biogenic volatile organic compound sources in late glacial and Holocene fluctuations of atmospheric methane concentrations , 2006 .

[12]  B. Alemán,et al.  Self-propelled Leidenfrost droplets. , 2006, Physical review letters.

[13]  T. Stocker,et al.  Isotope calibrated Greenland temperature record over Marine Isotope Stage 3 and its relation to CH4 , 2006 .

[14]  T. Sowers Late Quaternary Atmospheric CH4 Isotope Record Suggests Marine Clathrates Are Stable , 2006, Science.

[15]  F. Keppler,et al.  Methane emissions from terrestrial plants under aerobic conditions , 2006, Nature.

[16]  D. Etheridge,et al.  Unexpected Changes to the Global Methane Budget over the Past 2000 Years , 2005, Science.

[17]  J. Barnola,et al.  Records of the δ13C of atmospheric CH4 over the last 2 centuries as recorded in Antarctic snow and ice , 2005 .

[18]  W. Brand,et al.  Kel-F discs improve storage time of canopy air samples in 10-mL vials for CO2-delta13C analysis. , 2004, Rapid communications in mass spectrometry : RCM.

[19]  T. Stocker,et al.  N2O and CH4 variations during the last glacial epoch: Insight into global processes , 2004 .

[20]  Chapter 14 – Stable isotope measurements of atmospheric CO2 and CH4 , 2004 .

[21]  J. Schmitt,et al.  Amount-dependent isotopic fractionation during compound-specific isotope analysis. , 2003, Rapid communications in mass spectrometry : RCM.

[22]  E. Dlugokencky,et al.  Development of analytical methods and measurements of 13C/12C in atmospheric CH4 from the NOAA Climate Monitoring and Diagnostics Laboratory Global Air Sampling Network , 2002 .

[23]  W. Sturges,et al.  Changes in the global atmospheric methane budget over the last decades inferred from13C and D isotopic analysis of Antarctic firn air , 2001 .

[24]  S. Tyler,et al.  High-Precision Continuous-Flow Measurement of δ13C and δD of Atmospheric CH4 , 2001 .

[25]  W. Brand,et al.  Referencing strategies and techniques in stable isotope ratio analysis. , 2001, Rapid communications in mass spectrometry : RCM.

[26]  J. Hayes,et al.  Determination of the the H3 factor in hydrogen isotope ratio monitoring mass spectrometry. , 2001, Analytical chemistry.

[27]  J. Hayes,et al.  Correction of H3+ contributions in hydrogen isotope ratio monitoring mass spectrometry. , 2001, Analytical chemistry.

[28]  Behl,et al.  Carbon isotopic evidence for methane hydrate instability during quaternary interstadials , 2000, Science.

[29]  B. Stauffer,et al.  Changes in the atmospheric CH4 gradient between Greenland and Antarctica during the Last Glacial and the transition to the Holocene , 2000 .

[30]  Routine analysis by high precision gas chromatography/mass selective detector/isotope ratio mass spectrometry to 0.1 parts per mil. , 1999, Rapid communications in mass spectrometry : RCM.

[31]  E. Dlugokencky,et al.  The isotopic composition of atmospheric methane , 1999 .

[32]  J. Hayes,et al.  Quantitative Production of H2 by Pyrolysis of Gas Chromatographic Effluents , 1998 .

[33]  T. Stocker,et al.  Asynchrony of Antarctic and Greenland climate change during the last glacial period , 1998, Nature.

[34]  W. Meier-Augenstein A reference gas inlet module for internal isotopic calibration in high precision gas chromatography/combustion-isotope ratio mass spectrometry , 1997 .

[35]  H. Tobias,et al.  On-line pyrolysis as a limitless reduction source for high-precision isotopic analysis of organic-derived hydrogen. , 1997, Analytical chemistry.

[36]  Jerome Chappellaz,et al.  Changes in the atmospheric CH4 gradient between Greenland and Antarctica during the Holocene , 1997 .

[37]  K. Leckrone,et al.  Efficiency and temperature dependence of water removal by membrane dryers. , 1997, Analytical chemistry.

[38]  E. Brook,et al.  Rapid Variations in Atmospheric Methane Concentration During the Past 110,000 Years , 1996, Science.

[39]  H. Tobias,et al.  High-precision D/H measurement from hydrogen gas and water by continuous-flow isotope ratio mass spectrometry. , 1995, Analytical chemistry.

[40]  J. Hayes,et al.  Carbon isotopic analysis of atmospheric methane by isotope-ratio-monitoring gas chromatography-mass spectrometry. , 1995, Journal of geophysical research.

[41]  J. Hayes,et al.  Factors controlling precision and accuracy in isotope-ratio-monitoring mass spectrometry. , 1994, Analytical chemistry.

[42]  J. Hayes,et al.  Acquisition and processing of data for isotope-ratio-monitoring mass spectrometry. , 1994, Organic geochemistry.

[43]  B. Stauffer,et al.  The age of the air in the firn and the ice at Summit, Greenland , 1993 .

[44]  Duncan J. Wingham,et al.  NEW TECHNIQUES IN SATELLITE ALTIMETER TRACKING SYSTEMS. , 1986 .

[45]  I. Friedman,et al.  Deuterium content of natural waters and other substances , 1953 .