Markus Leuenberger

One-to-one coupling of glacial climate variability in Greenland and Antarctica.

Precise knowledge of the phase relationship between climate changes in the two hemispheres is a key for understanding the Earth’s climate dynamics. For the last glacial period, ice core studies have revealed strong coupling of the largest millennial-scale warm events in Antarctica with the longest Dansgaard–Oeschger events in Greenland through the Atlantic meridional overturning circulation. It has been unclear, however, whether the shorter Dansgaard–Oeschger events have counterparts in the shorter and less prominent Antarctic temperature variations, and whether these events are linked by the same mechanism. Here we present a glacial climate record derived from an ice core from Dronning Maud Land, Antarctica, which represents South Atlantic climate at a resolution comparable with the Greenland ice core records. After methane synchronization with an ice core from North Greenland, the oxygen isotope record from the Dronning Maud Land ice core shows a one-to-one coupling between all Antarctic warm events and Greenland Dansgaard–Oeschger events by the bipolar seesaw6. The amplitude of the Antarctic warm events is found to be linearly dependent on the duration of the concurrent stadial in the North, suggesting that they all result from a similar reduction in the meridional overturning circulation.

Carbon Isotope Constraints on the Deglacial CO2 Rise from Ice Cores

By the Numbers As carbon dioxide is exchanged between the atmosphere, the oceans, and the terrestrial biosphere, its carbon isotopic composition is modified by various processes involved in its transfer between the different reservoirs. The carbon isotopic composition of the carbon dioxide contained in bubbles of air trapped in ice cores thus provides a record of the processes that regulated the composition of the atmosphere in the past. Using data from three Antarctic ice cores, Schmitt et al. (p. 711, published online 29 March; see the Perspective by Brook) present a record of the carbon isotopic makeup of atmospheric CO2 for the past 24,000 years. The findings reveal the dominant role of the oceans during the early part of the deglaciation and the effects of the regrowth of the terrestrial biosphere later in the deglacial transition. Before the deglaciation, during the Last Glacial Maximum, the carbon cycle was essentially at equilibrium. The stable isotopic composition of the carbon in carbon dioxide over the last 24,000 years illuminates past carbon cycle behavior. The stable carbon isotope ratio of atmospheric CO2 (δ13Catm) is a key parameter in deciphering past carbon cycle changes. Here we present δ13Catm data for the past 24,000 years derived from three independent records from two Antarctic ice cores. We conclude that a pronounced 0.3 per mil decrease in δ13Catm during the early deglaciation can be best explained by upwelling of old, carbon-enriched waters in the Southern Ocean. Later in the deglaciation, regrowth of the terrestrial biosphere, changes in sea surface temperature, and ocean circulation governed the δ13Catm evolution. During the Last Glacial Maximum, δ13Catm and atmospheric CO2 concentration were essentially constant, which suggests that the carbon cycle was in dynamic equilibrium and that the net transfer of carbon to the deep ocean had occurred before then.

Changing boreal methane sources and constant biomass burning during the last termination

Past atmospheric methane concentrations show strong fluctuations in parallel to rapid glacial climate changes in the Northern Hemisphere superimposed on a glacial–interglacial doubling of methane concentrations. The processes driving the observed fluctuations remain uncertain but can be constrained using methane isotopic information from ice cores. Here we present an ice core record of carbon isotopic ratios in methane over the entire last glacial–interglacial transition. Our data show that the carbon in atmospheric methane was isotopically much heavier in cold climate periods. With the help of a box model constrained by the present data and previously published results, we are able to estimate the magnitude of past individual methane emission sources and the atmospheric lifetime of methane. We find that methane emissions due to biomass burning were about 45u2009Tg methane per year, and that these remained roughly constant throughout the glacial termination. The atmospheric lifetime of methane is reduced during cold climate periods. We also show that boreal wetlands are an important source of methane during warm events, but their methane emissions are essentially shut down during cold climate conditions.

Stable isotope constraints on Holocene carbon cycle changes from an Antarctic ice core

Reconstructions of atmospheric CO2 concentrations based on Antarctic ice cores reveal significant changes during the Holocene epoch, but the processes responsible for these changes in CO2 concentrations have not been unambiguously identified. Distinct characteristics in the carbon isotope signatures of the major carbon reservoirs (ocean, biosphere, sediments and atmosphere) constrain variations in the CO2 fluxes between those reservoirs. Here we present a highly resolved atmospheric δ13C record for the past 11,000u2009years from measurements on atmospheric CO2 trapped in an Antarctic ice core. From mass-balance inverse model calculations performed with a simplified carbon cycle model, we show that the decrease in atmospheric CO2 of about 5u2009parts per million by volume (p.p.m.v.). The increase in δ13C of about 0.25‰ during the early Holocene is most probably the result of a combination of carbon uptake of about 290 gigatonnes of carbon by the land biosphere and carbon release from the ocean in response to carbonate compensation of the terrestrial uptake during the termination of the last ice age. The 20u2009p.p.m.v. increase of atmospheric CO2 and the small decrease in δ13C of about 0.05‰ during the later Holocene can mostly be explained by contributions from carbonate compensation of earlier land-biosphere uptake and coral reef formation, with only a minor contribution from a small decrease of the land-biosphere carbon inventory.

Pooled versus separate measurements of tree-ring stable isotopes.

δ(13)C and δ(18)O of tree rings contain time integrated information about the environmental conditions weighted by seasonal growth dynamics and are well established as sources of palaeoclimatic and ecophysiological data. Annually resolved isotope chronologies are frequently produced by pooling dated growth rings from several trees prior to the isotopic analyses. This procedure has the advantage of saving time and resources, but precludes from defining the isotopic error or statistical uncertainty related to the inter-tree variability. Up to now only a few studies have compared isotope series from pooled tree rings with isotopic measurements from individual trees. We tested whether or not the δ(13)C and the δ(18)O chronologies derived from pooled and from individual tree rings display significant differences at two locations from the Iberian Peninsula to assess advantages and constraints of both methodologies. The comparisons along the period 1900-2003 reveal a good agreement between pooled chronologies and the two mean master series which were created by averaging raw individual values (Mean) or by generating a mass calibrated mean (MassC). In most of the cases, pooled chronologies show high synchronicity with averaged individual samples at interannual scale but some differences also show up especially when comparing δ(18)O decadal to multi-decadal variations. Moreover, differences in the first order autocorrelation among individuals may be obscured by pooling strategies. The lack of replication of pooled chronologies prevents detection of a bias due to a higher mass contribution of one sample but uncertainties associated with the analytical process itself, as sample inhomogeneity, seems to account for the observed differences.

A global picture of the first abrupt climatic event occurring during the last glacial inception

The orbital-scale transition from the last interglacial to glacial climate corresponds to the progressive organization of global millennial-scale climate variability. Here, we investigate the struc ...

Measurements of the 17O excess in water with the equilibration method.

The equilibration method is the present-day standard method for measuring delta18O in water samples. The mass-to-charge ratio of 45 is measured at the same time but generally not used for further analysis. We show that an improved equilibration method can be used for precise determination of delta17O in addition to that of delta18O, and therefore can estimate 17O excess values to a precision of better than 0.1 per thousand. To control the masking effect of the 14 times more abundant 13C on mass 45, we propose to use a chemical buffer in the water samples to keep the pH value and therefore the fractionation during the equilibration process of the 13C constant. With this improved method, the precision for the delta18O value could also be slightly improved from 0.05 to 0.03 per thousand. Furthermore, we discuss the influences of the amount of water, the temperature, the CO2 gas pressures, and changes in the pH during the measuring procedure on oxygen and carbon isotopes. We noticed that measured delta45 values are a good control for delta18O measurements. This study tries to fathom the possibilities and limitations of the equilibration method for measuring 17O excess values of water samples.