Export 7 results:
Sort by: Author Title Type [ Year  (Desc)]
Rosen, JL, Brook EJ, Severinghaus JP, Blunier T, Mitchell LE, Lee JE, Edwards JS, Gkinis V.  2014.  An ice core record of near-synchronous global climate changes at the Bolling transition. Nature Geoscience. 7:459-463.   10.1038/ngeo2147   AbstractWebsite

The abrupt warming that initiated the Bolling-Allerod interstadial was the penultimate warming in a series of climate variations known as Dansgaard-Oeschger events. Despite the clear expression of this transition in numerous palaeoclimate records, the relative timing of climate shifts in different regions of the world and their causes are subject to debate. Here we explore the phasing of global climate change at the onset of the Bolling-Allerod using air preserved in bubbles in the North Greenland Eemian ice core. Specifically, we measured methane concentrations, which act as a proxy for low-latitude climate, and the N-15/N-14 ratio of N-2, which reflects Greenland surface temperature, over the same interval of time. We use an atmospheric box model and a firn air model to account for potential uncertainties in the data, and find that changes in Greenland temperature and atmospheric methane emissions at the Bolling onset occurred essentially synchronously, with temperature leading by 4.5(-24)(+21) years. We cannot exclude the possibility that tropical climate could iag changing methane concentrations by up to several decades, if the initial methane rise came from boreal sources alone. However, because even boreal methane-producing regions lie far from Greenland, we conclude that the mechanism that drove abrupt change at this time must be capable of rapidly transmitting climate changes across the globe.

Brook, EJ, Severinghaus JP.  2011.  Methane and megafauna. Nature Geoscience. 4:271-272.   10.1038/ngeo1140   AbstractWebsite
Grachev, AM, Brook EJ, Severinghaus JP, Pisias NG.  2009.  Relative timing and variability of atmospheric methane and GISP2 oxygen isotopes between 68 and 86 ka. Global Biogeochemical Cycles. 23   10.1029/2008gb003330   AbstractWebsite

The global biogeochemical cycle of methane has received wide attention because of methane's role as a greenhouse gas. Measurements of methane in air trapped in Greenland ice cores provide a high-resolution record of methane levels in the atmosphere over the past similar to 100 ka, providing clues about what controls the methane cycle on geologic timescales. Remarkable similarity between local temperature recorded in Greenland ice cores and changes in global methane concentrations has been noted in previous studies, with the inference that the local temperature variations have global significance, but the resolution of sampling and measurement precision limited fine-scale comparison of these variables. In this work a higher-precision (similar to 2 ppb) methane data set was obtained from the Greenland Ice Sheet Project 2 (GISP2) ice core for the time interval between 86 and 68 ka, encompassing three large abrupt warming events early in the last glacial period: Dansgaard-Oeschger (D-O) events 19, 20, and 21. The new data set consists of duplicate measurements at 158 depths, with average time resolution of 120 years. Such detailed measurements over D-O 21, the longest in Greenland records, have not yet been reported for other ice cores. The new data set documents short-term variability (similar to 20 ppb typical amplitude), which is remarkably persistent, and in many cases similar features are observed in the most detailed published delta(18)O(ice) record. High-precision GISP2 delta(15)N data show that changes in Greenland temperature are synchronous with the methane variations at the onset of D-O events 19, 20, and 21, supporting previous results from the Greenland Ice Core Project ice core for D-O 19 and 20. Cross-spectral analysis quantifies the extremely close similarity between the new methane record and the delta(18)O(ice) record. Because methane sources are widely distributed over the globe, this work further validates delta(18)O(ice) at Greenland summit as a geographically broad climate indicator on millennial to multicentennial timescales.

Grachev, AM, Brook EJ, Severinghaus JP.  2007.  Abrupt changes in atmospheric methane at the MIS 5b-5a transition. Geophysical Research Letters. 34   10.1029/2007gl029799   AbstractWebsite

New ice core analyses show that the prominent rise in atmospheric methane concentration at Dansgaard-Oeschger event 21 was interrupted by a century-long 20% decline, which was previously unrecognized. The reversal was found in a new similar to 100-year resolution study of methane in the GISP2 ice core, encompassing the beginning of D-O event 21, which also corresponds to the transition from MIS 5b to 5a. Although a corresponding reversal (within age uncertainty) is observed in climate proxies measured in GISP2 ice, including delta O-18(ice), electrical conductivity, light scattering, and several ions, this feature has not been discussed previously. Abrupt changes in methane are paralleled by changes in delta N-15 of trapped air, a quantity that reflects local temperature change at Greenland summit. The reversal described here supports the hypothesis that climate can be unstable during major transitions, as was previously described for the last deglaciation.

Huber, C, Beyerle U, Leuenberger M, Schwander J, Kipfer R, Spahni R, Severinghaus JP, Weiler K.  2006.  Evidence for molecular size dependent gas fractionation in firn air derived from noble gases, oxygen, and nitrogen measurements. Earth and Planetary Science Letters. 243:61-73.   10.1016/j.epsl.2005.12.036   AbstractWebsite

We present elemental and isotopic measurements of noble gases (He, Ne, Ar, Kr, and Xe), oxygen and nitrogen of firn air from two sites. The first set of samples was taken in 1998 at the summit of the Devon Ice Cap in the eastern part of Devon Island. The second set was taken in 2001 at NGRIP location (North Greenland). He and Ne are heavily enriched relative to Ar with respect to the atmosphere in the air near the close-off depth at around 50-70 in. The enrichment increases with depth and reaches the maximum value in the deepest samples just above the zone of impermeable ice where no free air could be extracted anymore. Similarly, elemental ratios of O(2)/N(2), O(2)/Ar and Ar/N(2) are increasing with depth. In contrast but in line with expectations, isotopic ratios of (15)N/(14)N, (18)O/(16)O, and (36)Ar/(40)Ar show no significant enrichment near the close-off depth. The observed isotopic ratios in the firn air column can be explained within the uncertainty ranges by the well-known processes of gravitational enrichment and thermal diffusion. To explain the elemental ratios, however, an additional fractionation process during bubble inclusion has to be considered. We implemented this additional process into our firn air model. The fractionation factors were found by fitting model profiles to the data. We found a very similar close-off fractionation behavior for the different molecules at both sites. For smaller gas species (mainly He and Ne) the fractionation factors are linearly correlated to the molecule size, whereas for diameters greater than about 3.6 A the fractionation seems to be significantly smaller or even negligible. An explanation for this size dependent fractionation process could be gas diffusion through the ice lattice. At Devon Island the enrichment at the bottom of the firn air column is about four times higher compared to NGRIP. We explain this by lower firn diffusivity at Devon Island, most probably due to melt layers, resulting in significantly reduced back diffusion of the excess gas near the close-off depth. The results of this study considerably increase the understanding of the processes occurring during air bubble inclusion near the close-off depth in firn and can help to improve the interpretation of direct firn air measurements, as well as air bubble measurements in ice cores, which are used in numerous studies as paleo proxies. (c) 2006 Elsevier B.V. All rights reserved.

Caillon, N, Jouzel J, Severinghaus JP, Chappellaz J, Blunier T.  2003.  A novel method to study the phase relationship between Antarctic and Greenland climate. Geophysical Research Letters. 30   10.1029/2003gl017838   AbstractWebsite

A classical method for understanding the coupling between northern and southern hemispheres during millennial-scale climate events is based on the correlation between Greenland and Antarctic ice core records of atmospheric composition. Here we present a new approach based on the use of a single Antarctic ice core in which measurements of methane concentration and inert gas isotopes place constraints on the timing of a rapid climate change in the North and of its Antarctic counterpart. We applied it to the Marine Isotope Stage (MIS) 5d/c transition early in the last glaciation similar to108 ky BP. Our results indicate that the Antarctic temperature increase occurred 2 ky before the methane increase, which is used as a time marker of the warming in the Northern Hemisphere. This result is in agreement with the "bipolar seesaw'' mechanism used to explain the phase relationships documented between 23 and 90 ky BP [Blunier and Brook, 2001].

Brook, EJ, Harder S, Severinghaus J, Steig EJ, Sucher CM.  2000.  On the origin and timing of rapid changes in atmospheric methane during the last glacial period. Global Biogeochemical Cycles. 14:559-572.   10.1029/1999gb001182   AbstractWebsite

We present high resolution records of atmospheric methane from the GISP2 (Greenland Ice Sheet Project 2) ice core for four rapid climate transitions that occurred during the past 50 ka: the end of the Younger Dryas at 11.8 ka, the beginning of the Bolling-Allerod period at 14.8 ka, the beginning of interstadial 8 at 38.2 ka, and the beginning of interstadial 12 at 45.5 ka. During these events, atmospheric methane concentrations increased by 200-300 ppb over time periods of 100-300 years, significantly more slowly than associated temperature and snow accumulation changes recorded in the ice core record. We suggest that the slower rise in methane concentration may reflect the timescale of terrestrial ecosystem response to rapid climate change. We find no evidence for rapid, massive methane emissions that might be associated with large-scale decomposition of methane hydrates in sediments. With additional results from the Taylor Dome Ice Core (Antarctica) we also reconstruct changes in the interpolar methane gradient tan indicator of the geographical distribution of methane sources) associated with some of the rapid changes in atmospheric methane. The results indicate that the rise in methane at the beginning of the Bolling-Allerod period and the later rise at the end of the Younger Dryas were driven by increases in both tropical and boreal methane sources. During the Younger Dryas (a 1.3 ka cold period during the last deglaciation) the relative contribution from boreal sources was reduced relative to the early and middle Holocene periods.