Olivier Cattani

Eight glacial cycles from an Antarctic ice core

The Antarctic Vostok ice core provided compelling evidence of the nature of climate, and of climate feedbacks, over the past 420,000 years. Marine records suggest that the amplitude of climate variability was smaller before that time, but such records are often poorly resolved. Moreover, it is not possible to infer the abundance of greenhouse gases in the atmosphere from marine records. Here we report the recovery of a deep ice core from Dome C, Antarctica, that provides a climate record for the past 740,000 years. For the four most recent glacial cycles, the data agree well with the record from Vostok. The earlier period, between 740,000 and 430,000 years ago, was characterized by less pronounced warmth in interglacial periods in Antarctica, but a higher proportion of each cycle was spent in the warm mode. The transition from glacial to interglacial conditions about 430,000 years ago (Termination V) resembles the transition into the present interglacial period in terms of the magnitude of change in temperatures and greenhouse gases, but there are significant differences in the patterns of change. The interglacial stage following Termination V was exceptionally long—28,000 years compared to, for example, the 12,000 years recorded so far in the present interglacial period. Given the similarities between this earlier warm period and today, our results may imply that without human intervention, a climate similar to the present one would extend well into the future.The Antarctic Vostok ice core provided compelling evidence of the nature of climate, and of climate feedbacks, over the past 420,000 years. Marine records suggest that the amplitude of climate variability was smaller before that time, but such records are often poorly resolved. Moreover, it is not possible to infer the abundance of greenhouse gases in the atmosphere from marine records. Here we report the recovery of a deep ice core from Dome C, Antarctica, that provides a climate record for the past 740,000 years. For the four most recent glacial cycles, the data agree well with the record from Vostok. The earlier period, between 740,000 and 430,000 years ago, was characterized by less pronounced warmth in interglacial periods in Antarctica, but a higher proportion of each cycle was spent in the warm mode. The transition from glacial to interglacial conditions about 430,000 years ago (Termination V) resembles the transition into the present interglacial period in terms of the magnitude of change in temperatures and greenhouse gases, but there are significant differences in the patterns of change. The interglacial stage following Termination V was exceptionally long—28,000 years compared to, for example, the 12,000 years recorded so far in the present interglacial period. Given the similarities between this earlier warm period and today, our results may imply that without human intervention, a climate similar to the present one would extend well into the future.

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.

A Review of Antarctic Surface Snow Isotopic Composition: Observations, Atmospheric Circulation, and Isotopic Modeling*

A database of surface Antarctic snow isotopic composition is constructed using available measurements, with an estimate of data quality and local variability. Although more than 1000 locations are documented, the spatial coverage remains uneven with a majority of sites located in specific areas of East Antarctica. The database is used to analyze the spatial variations in snow isotopic composition with respect to geographical characteristics (elevation, distance to the coast) and climatic features (temperature, accumulation) and with a focus on deuterium excess. The capacity of theoretical isotopic, regional, and general circulation atmospheric models (including “isotopic” models) to reproduce the observed features and assess the role of moisture advection in spatial deuterium excess fluctuations is analyzed.

A new 27 ky high resolution East Antarctic climate record

The ice core recently drilled at the Dome Concordia site on the East Antarctic plateau provides a new high resolution isotope record covering part of the last glacial, the last transition and the Holocene. The two step shape of the deglaciation is remarkably similar for all the ice cores now available on the East Antarctic plateau. The first warming trend ends about 14000 years ago and is followed by the well marked Antarctic Cold Reversal (ACR) with a secondary peak common to all records. During the deglaciation, there are more similarities between the near coastal site of Taylor Dome and inland East Antarctica than between Taylor Dome and central Greenland. However, the results for EPICA do appear to confirm the Taylor Dome timescale after about 14 ka, showing cooling into the ACR roughly in phase between Greenland and Antarctica. While the overall deglacial pattern is asynchronous, this suggests that the now classical picture of a temperature seesaw between Antarctica and Greenland may be too simplistic.

10Be evidence for the Matuyama-Brunhes geomagnetic reversal in the EPICA Dome C ice core.

An ice core drilled at Dome C, Antarctica, is the oldest ice core so far retrieved. On the basis of ice flow modelling and a comparison between the deuterium signal in the ice with climate records from marine sediment cores, the ice at a depth of 3,190 m in the Dome C core is believed to have been deposited around 800,000 years ago, offering a rare opportunity to study climatic and environmental conditions over this time period. However, an independent determination of this age is important because the deuterium profile below a depth of 3,190 m depth does not show the expected correlation with the marine record. Here we present evidence for enhanced 10Be deposition in the ice at 3,160–3,170 m, which we interpret as a result of the low dipole field strength during the Matuyama–Brunhes geomagnetic reversal, which occurred about 780,000 years ago. If correct, this provides a crucial tie point between ice cores, marine cores and a radiometric timescale.

A late-glacial high-resolution site and source temperature record derived from the EPICA Dome C isotope records (East Antarctica)

The timing and synchronisation of Greenland and Antarctic climate events that occurred during the last glacial period are still under debate, as is the magnitude of temperature change associated with these events. Here we present detailed records of local and moisture-source temperature changes spanning the period 27-45 kyr BP from water stable isotope measurements (deltaD and delta(18)O) in the recently drilled EPICA Dome C ice core, East Antarctic plateau. Using a simple isotopic model, site (DeltaT(site)) and source (DeltaT(source)) temperatures are extracted from the initial 50-yr high-resolution isotopic records, taking into account the changes in seawater isotopic composition. The deuterium isotope variability is very similar to the less precise deltaD record from the Vostok ice core, and the site temperature inversion leads to a temperature profile similar to the classical palaeothermometry method, due to compensations between source and ocean water corrections. The reconstructed DeltaT(site) and DeltaT(source) profiles show different trends during the glacial: the former shows a decreasing trend from the warm Al event (38 kyr BP) toward the Last Glacial Maximum, while the latter shows increasing values from 41 to 28 kyr BP. The low-frequency deuterium excess fluctuations are strongly influenced by obliquity fluctuations, controlling the low- to high-latitude temperature gradients, and show a remarkable similarity with a high-resolution southeast Atlantic sea surface temperature record. A comparison of the temperature profiles (site and source) and temperature gradient (DeltaT(source)-DeltaT(site)) with the non-sea-salt calcium and sodium records suggests a secondary influence of atmospheric transport changes on aerosol variations.

Fossil water in large stalagmite voids as a tool for paleoprecipitation stable isotope composition reconstitution and paleotemperature calculation

The deuterium content of macroscopic fluid inclusions, several millimetres large, observed on two stalagmite polished sections has been measured with high accuracy (<F0.5x). Although several recent studies have already focused on the stable isotope content of microscopic fluid inclusions, this is the first time that such measurements have been made on large inclusions by direct injection of the water in the spectrometer, eliminating technical problems due to the extraction of water from microscopic inclusions (crushing and heating). The first results from four fluid inclusions of two stalagmites of South Western and Southern France demonstrate that: (1) for the same stalagmite and the same age, the deuterium content is similar; (2) the fluid inclusion deuterium content difference between the sites is in agreement with the present day dripping water; (3) calculated paleotemperatures at 100 ka are in the range of those derived from pollen, marine and ice core records. Despite the fact that macroscopic fluid inclusions have rarely been observed, it appears that they can give precious data for paleoclimatologists on the stable isotope content (d 18 O, dD and deuterium excess d) of the past cave dripping water, which is a proxy of the rainfall water, and that it can be accurately dated by the TIMS U/Th method on the host calcite up to 500 ka. D 2002 Elsevier Science B.V. All rights reserved.

Water isotope ratio (δ2H and δ18O) measurements in atmospheric moisture using an optical feedback cavity enhanced absorption laser spectrometer

Water vapor isotopes represent an innovative and excellent tool for understanding complex mechanisms in the atmospheric water cycle over different time scales, and they can be used for a variety of applications in the fields of paleoclimatology, hydrology, oceanography, and ecology. We use an ultrasensitive near-infrared spectrometer, originally designed for use on airborne platforms in the upper troposphere and lower stratosphere, to measure the water deuterium and oxygen-18 isotope ratios in situ, in ground-level tropospheric moisture, with a high temporal resolution (from 300 s down to less than 1 s). We present some examples of continuous monitoring of near-surface atmospheric moisture, demonstrating that our infrared laser spectrometer could be used successfully to record high-concentration atmospheric water vapor mixing ratios in continuous time series, with a data coverage of similar to 90%, interrupted only for daily calibration to two isotope ratio mass spectrometry-calibrated local water standards. The atmospheric data show that the water vapor isotopic composition exhibits a high variability that can be related to weather conditions, especially to changes in relative humidity. Besides, the results suggest that observed spatial and temporal variations of the stable isotope content of atmospheric water vapor are strongly related to water vapor transport in the atmosphere.

The isotopic composition of water vapour and precipitation in Ivittuut, southern Greenland

Since September 2011, a wavelength-scanned cavity ring-down spectroscopy analyser has been remotely operated in Ivittuut, southern Greenland, providing the first record of surface water vapour isotopic composition based on continuous measurements in South Greenland and the first record including the winter season in Greenland. The comparison of vapour data with measurements of precipitation isotopic composition suggest an equilibrium between surface vapour and precipitation. δ18O and deuterium excess are generally anti-correlated and show important seasonal variations, with respective amplitudes of∼ 10 and∼ 20 ‰, as well as large synoptic variations. The data depict small summer diurnal variations. At the seasonal scale, δ18O has a minimum in November– December and a maximum in June–July, while deuterium excess has a minimum in May–June and a maximum in November. The approach of low-pressure systems towards South Greenland leads to δ18O increase (typically+5 ‰) and deuterium excess decrease (typically −15 ‰). Seasonal and synoptic variations coincide with shifts in the moisture sources, estimated using a quantitative moisture source diagnostic based on a Lagrangian back-trajectory model. The atmospheric general circulation model LMDZiso correctly captures the seasonal and synoptic variability of δ18O, but does not capture the observed magnitude of deuterium excess variability. Covariations of water vapour isotopic composition with local and moisture source meteorological parameters have been evaluated. δ18O is strongly correlated with the logarithm of local surface humidity, consistent with Rayleigh distillation processes, and with local surface air temperature, associated with a slope of ∼ 0.4 ‰◦C−1. Deuterium excess correlates with local surface relative humidity as well as surface relative humidity from the dominant moisture source area located in the North Atlantic, south of Greenland and Iceland.

Measurements of water vapor isotope ratios with wavelength-scanned cavity ring-down spectroscopy technology: new insights and important caveats for deuterium excess measurements in tropical areas in comparison with isotope-ratio mass spectrometry

The new infrared laser spectroscopic techniques enable us to measure the isotopic composition (δ(18)O and δ(2)H) of atmospheric water vapor. With the objective of monitoring the isotopic composition of tropical water vapor (West Africa, South America), and to discuss deuterium excess variability (d=δ(2)H - 8δ(18)O) with an accuracy similar to measurements arising from isotope-ratio mass spectrometry (IRMS), we have conducted a number of tests and calibrations using a wavelength-scanned cavity ring-down spectroscopy (WS-CRDS) technique. We focus in this paper on four main aspects regarding (1) the tubing material, (2) the humidity calibration of the instrument, (3) the water vapor concentration effects on δ, and (4) the isotopic calibration of the instrument. First, we show that Synflex tubing strongly affects δ(2)H measurements and thus leads to unusable d values. Second, we show that the mixing ratio as measured by WS-CRDS has to be calibrated versus atmospheric mixing ratio measurements and we also suggest possible non-linear effects over the whole mixing ratio range (~2 to 20 g/kg). Third, we show that significant non-linear effects are induced by water vapor concentration variations on δ measurements, especially for mixing ratios lower than ~5 g/kg. This effect induces a 5 to 10‰ error in deuterium excess and is instrument-dependent. Finally, we show that an isotopic calibration (comparison between measured and true values of isotopic water standards) is needed to avoid errors on deuterium excess that can attain ~10‰.