Publications

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Book Chapter
Atwater, T, Sclater J, Sandwell D, Severinghaus J, Marlow M.  1993.  Fracture zone traces across the North Pacific Cretaceous Quiet Zone and their tectonic implications. The Mesozoic Pacific : geology, tectonics, and volcanism : a volume in memory of Sy Schlanger. ( Pringle MS, Sager WW, Sliter WV, Stein S, Eds.).:137-154., Washington, DC: American Geophysical Union Abstract
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Journal Article
Petrenko, VV, Martinerie P, Novelli P, Etheridge DM, Levin I, Wang Z, Blunier T, Chappellaz J, Kaiser J, Lang P, Steele LP, Hammer S, Mak J, Langenfelds RL, Schwander J, Severinghaus JP, Witrant E, Petron G, Battle MO, Forster G, Sturges WT, Lamarque JF, Steffen K, White JWC.  2013.  A 60 yr record of atmospheric carbon monoxide reconstructed from Greenland firn air. Atmospheric Chemistry and Physics. 13:7567-7585.   10.5194/acp-13-7567-2013   AbstractWebsite

We present the first reconstruction of the Northern Hemisphere (NH) high latitude atmospheric carbon monoxide (CO) mole fraction from Greenland firn air. Firn air samples were collected at three deep ice core sites in Greenland (NGRIP in 2001, Summit in 2006 and NEEM in 2008). CO records from the three sites agree well with each other as well as with recent atmospheric measurements, indicating that CO is well preserved in the firn at these sites. CO atmospheric history was reconstructed back to the year 1950 from the measurements using a combination of two forward models of gas transport in firn and an inverse model. The reconstructed history suggests that Arctic CO in 1950 was 140-150 nmol mol(-1), which is higher than today's values. CO mole fractions rose by 10-15 nmol mol(-1) from 1950 to the 1970s and peaked in the 1970s or early 1980s, followed by a approximate to 30 nmol mol(-1) decline to today's levels. We compare the CO history with the atmospheric histories of methane, light hydrocarbons, molecular hydrogen, CO stable isotopes and hydroxyl radicals (OH), as well as with published CO emission inventories and results of a historical run from a chemistry-transport model. We find that the reconstructed Greenland CO history cannot be reconciled with available emission inventories unless unrealistically large changes in OH are assumed. We argue that the available CO emission inventories strongly underestimate historical NH emissions, and fail to capture the emission decline starting in the late 1970s, which was most likely due to reduced emissions from road transportation in North America and Europe.

Taylor, KC, White JWC, Severinghaus JP, Brook EJ, Mayewski PA, Alley RB, Steig EJ, Spencer MK, Meyerson E, Meese DA, Lamorey GW, Grachev A, Gow AJ, Barnett BA.  2004.  Abrupt climate change around 22 ka on the Siple Coast of Antarctica. Quaternary Science Reviews. 23:7-15.   10.1016/j.quascirev.2003.09.004   AbstractWebsite

A new ice core from Siple Dome, Antarctica suggests the surface temperature increased by similar to6degreesC in just several decades at approximately 22 ka BP. This abrupt change did not occur 500 kin away in the Byrd ice core, or in climate proxy records in the Siple Dome core indicative of the mid-latitude Pacific. This demonstrates there was significant spatial heterogeneity in the response of the Antarctic climate during the last deglaciation and draws attention to unexplained mechanisms of abrupt climate change in Antarctica. (C) 2003 Elsevier Ltd. All rights reserved.

Bauska, TK, Baggenstos D, Brook EJ, Mix AC, Marcott SA, Petrenko VV, Schaefer H, Severinghaus JP, Lee JE.  2016.  Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation. Proceedings of the National Academy of Sciences of the United States of America. 113:3465-3470.   10.1073/pnas.1513868113   AbstractWebsite

An understanding of the mechanisms that control CO2 change during glacial-interglacial cycles remains elusive. Here we help to constrain changing sources with a high-precision, high-resolution deglacial record of the stable isotopic composition of carbon in CO2 (delta C-13-CO2) in air extracted from ice samples from Taylor Glacier, Antarctica. During the initial rise in atmospheric CO2 from 17.6 to 15.5 ka, these data demarcate a decrease in delta C-13-CO2, likely due to a weakened oceanic biological pump. From 15.5 to 11.5 ka, the continued atmospheric CO2 rise of 40 ppm is associated with small changes in delta C-13-CO2, consistent with a nearly equal contribution from a further weakening of the biological pump and rising ocean temperature. These two trends, related to marine sources, are punctuated at 16.3 and 12.9 ka with abrupt, century-scale perturbations in delta C-13-CO2 that suggest rapid oxidation of organic land carbon or enhanced air-sea gas exchange in the Southern Ocean. Additional century-scale increases in atmospheric CO2 coincident with increases in atmospheric CH4 and Northern Hemisphere temperature at the onset of the Bolling (14.6-14.3 ka) and Holocene (11.6-11.4 ka) intervals are associated with small changes in delta C-13-CO2, suggesting a combination of sources that included rising surface ocean temperature.

Marcott, SA, Bauska TK, Buizert C, Steig EJ, Rosen JL, Cuffey KM, Fudge TJ, Severinghaus JP, Ahn J, Kalk ML, McConnell JR, Sowers T, Taylor KC, White JWC, Brook EJ.  2014.  Centennial-scale changes in the global carbon cycle during the last deglaciation. Nature. 514:616-+.   10.1038/nature13799   AbstractWebsite

Global climate and the concentration of atmospheric carbon dioxide (CO2) are correlated over recent glacial cycles(1,2). The combination of processes responsible for a rise in atmospheric CO2 at the last glacial termination(1,3) (23,000 to 9,000 years ago), however, remains uncertain(1-3). Establishing the timing and rate of CO2 changes in the past provides critical insight into the mechanisms that influence the carbon cycle and helps put present and future anthropogenic emissions in context. Here we present CO2 and methane (CH4) records of the last deglaciation from a new high-accumulation West Antarctic ice core with unprecedented temporal resolution and precise chronology. We show that although low-frequency CO2 variations parallel changes in Antarctic temperature, abrupt CO2 changes occur that have a clear relationship with abrupt climate changes in the Northern Hemisphere. A significant proportion of the direct radiative forcing associated with the rise in atmospheric CO2 occurred in three sudden steps, each of 10 to 15 parts per million. Every step took place in less than two centuries and was followed by no notable change in atmospheric CO2 for about 1,000 to 1,500 years. Slow, millennial-scale ventilation of Southern Ocean CO2-rich, deep-ocean water masses is thought to have been fundamental to the rise in atmospheric CO2 associated with the glacial termination(4), given the strong covariance of CO2 levels and Antarctic temperatures(5). Our data establish a contribution from an abrupt, centennial-scale mode of CO2 variability that is not directly related to Antarctic temperature. We suggest that processes operating on centennial timescales, probably involving the Atlantic meridional overturning circulation, seem to be influencing global carbon-cycle dynamics and are at present not widely considered in Earth system models.

Bauska, TK, Brook EJ, Marcott SA, Baggenstos D, Shackleton S, Severinghaus JP, Petrenko VV.  2018.  Controls on millennial-scale atmospheric CO2 variability during the last glacial period. Geophysical Research Letters. 45:7731-7740.   10.1029/2018gl077881   AbstractWebsite

Changes in atmospheric CO2 on millennial-to-centennial timescales are key components of past climate variability during the last glacial and deglacial periods (70-10 ka), yet the sources and mechanisms responsible for the CO2 fluctuations remain largely obscure. Here we report the C-13/C-12 ratio of atmospheric CO2 during a key interval of the last glacial period at submillennial resolution, with coeval histories of atmospheric CO2, CH4, and N2O concentrations. The carbon isotope data suggest that the millennial-scale CO2 variability in Marine Isotope Stage 3 is driven largely by changes in the organic carbon cycle, most likely by sequestration of respired carbon in the deep ocean. Centennial-scale CO2 variations, distinguished by carbon isotope signatures, are associated with both abrupt hydrological change in the tropics (e.g., Heinrich events) and rapid increases in Northern Hemisphere temperature (Dansgaard-Oeschger events). These events can be linked to modes of variability during the last deglaciation, thus suggesting that drivers of millennial and centennial CO2 variability during both periods are intimately linked to abrupt climate variability. Plain Language Summary Ice cores provide unique records of variations in atmospheric CO2 prior to the instrumental era. While it is clear that changes in atmospheric CO2 played a significant role in driving past climate change, it is unclear what in turn drove changes in atmospheric CO2. Here we investigate enigmatic changes in atmospheric CO2 levels during an interval of the last glacial period (similar to 50,000 to 35,000 years ago) that are associated with abrupt changes in polar climate. To determine the sources and sinks for atmospheric CO2, we measured the stable isotopes of carbon in CO2 and found that the primary source of carbon to the atmosphere was an organic carbon reservoir. Most likely, this carbon was sourced from a deep ocean reservoir that waxed and waned following changes in either the productivity of the surface ocean or stratification of the deep ocean. We also found that atmospheric CO2 can change on the centennial timescale during abrupt climate transitions in the Northern Hemisphere. This observation adds to a growing body of evidence that abrupt changes in atmospheric CO2 are an important component of past carbon cycle variability.

Battle, MO, Severinghaus JP, Sofen ED, Plotkin D, Orsi AJ, Aydin M, Montzka SA, Sowers T, Tans PP.  2011.  Controls on the movement and composition of firn air at the West Antarctic Ice Sheet Divide. Atmospheric Chemistry and Physics. 11:11007-11021.   10.5194/acp-11-11007-2011   AbstractWebsite

We sampled interstitial air from the perennial snowpack (firn) at a site near the West Antarctic Ice Sheet Divide (WAIS-D) and analyzed the air samples for a wide variety of gas species and their isotopes. We find limited convective influence (1.4-5.2 m, depending on detection method) in the shallow firn, gravitational enrichment of heavy species throughout the diffusive column in general agreement with theoretical expectations, a similar to 10 m thick lock-in zone beginning at similar to 67 m, and a total firn thickness consistent with predictions of Kaspers et al. (2004). Our modeling work shows that the air has an age spread (spectral width) of 4.8 yr for CO2 at the firn-ice transition. We also find that advection of firn air due to the 22 cm yr(-1) ice-equivalent accumulation rate has a minor impact on firn air composition, causing changes that are comparable to other modeling uncertainties and intrinsic sample variability. Furthermore, estimates of 1 age (the gas age/ice age difference) at WAIS-D appear to be largely unaffected by bubble closure above the lock-in zone. Within the lock-in zone, small gas species and their isotopes show evidence of size-dependent fractionation due to permeation through the ice lattice with a size threshold of 0.36 nm, as at other sites. We also see an unequivocal and unprecedented signal of oxygen isotope fractionation within the lock-in zone, which we interpret as the mass-dependent expression of a size-dependent fractionation process.

Kawamura, K, Severinghaus JP, Ishidoya S, Sugawara S, Hashida G, Motoyama H, Fujii Y, Aoki S, Nakazawa T.  2006.  Convective mixing of air in firn at four polar sites. Earth and Planetary Science Letters. 244:672-682.   10.1016/j.epsl.2006.02.017   AbstractWebsite

Air withdrawn from the firn, at four polar sites (Dome Fuji, H72 and YM85, Antarctica and North GRIP, Greenland) was measured for delta N-15 of N-2 and delta O-18 of O-2 to test for the presence of convective air mixing in the top part of the firn, known as the "convective zone". Understanding the convective zone and its possible relationship to surface conditions is important for constructing accurate ice-core greenhouse gas chronologies and their phasing with respect to climate change. The thickness of the convective zone was inferred from a regression line with barometric slope of the data in the deep firn. It is less than a few meters at H72 and NGRIP, whereas a substantial convective zone is found at Dome Fuji (8.6 +/- 2.6 m) and YM85 (14.0 +/- 1.8 m). By matching the outputs of a diffusion model to the data, effective eddy diffusivities required to mix the firn air are found. At the surface of Dome Fuji and YM85, these are found to be several times greater than the molecular diffusivity in free air. The crossover from dominance of convection to molecular diffusion takes place at 7 +/- 2, 11 +/- 2 and 0.5 +/- 0.5 m at Dome Fuji, YM85 and NGRIP, respectively. These depths can be used as an alternative definition of the convective zone thickness. The firn permeability at Dome Fuji is expected to be high because of intense firn metamorphism due to the low accumulation rate and large seasonal air temperature variation at the site. The firn layers in the top several meters are exposed to strong temperature gradients for several decades, leading to large firn grains and depth hoar that enhance permeability. The thick convective zone at YM85 is unexpected because the temperature, accumulation rate and near-surface density are comparable to NGRIP. The strong katabatic wind at YM85 is probably responsible for creating the deep convection. The largest convective zone found in this study is still only half of the current inconsistency implied from the deep ice core gas isotopes and firn densification models. (c) 2006 Elsevier B.V. All rights reserved.

Severinghaus, JP, Albert MR, Courville ZR, Fahnestock MA, Kawamura K, Montzka SA, Muhle J, Scambos TA, Shields E, Shuman CA, Suwa M, Tans P, Weiss RF.  2010.  Deep air convection in the firn at a zero-accumulation site, central Antarctica. Earth and Planetary Science Letters. 293:359-367.   10.1016/j.epsl.2010.03.003   AbstractWebsite

Ice cores provide unique archives of past atmospheres and climate, but interpretation of trapped-gas records and their climatic significance has been hampered by a poor knowledge of the prevalence of air convection in the firn layer on top of polar ice sheets. In particular, the phasing of greenhouse gases and climate from ice cores has been obscured by a discrepancy between empirical and model-based estimates of the age difference between trapped gases and enclosing ice, which may be due to air convection. Here we show that deep air convection (>23 m) occurs at a windy, near-zero-accumulation rate site in central Antarctica known informally as the Megadunes site (80.77914 degrees S, 124.48796 degrees E). Deep convection is evident in depth profiles of air withdrawn from the firn layer, in the observed pattern of the nitrogen isotope ratio (15)N/(14)N, the argon isotope ratio (40)Ar/(36)Ar, and in the mixing ratios of the anthropogenic halocarbons methyl chloroform (CH(3)CCl(3)) and HFC-134a (CH(2)FCF(3)). Transport parameters (diffusivities) were inferred and air was dated using measured carbon dioxide (CO(2)) and methane (CH(4)) mixing ratios, by comparing with the Law Dome atmospheric record, which shows that these are the oldest firn air samples ever recovered (CO(2) mean age = 1863 AD). The low accumulation rate and the consequent intense metamorphism of the firn (due to prolonged exposure to seasonal temperature cycling) likely contribute to deep air convection via large grain size and vertical cracks that act as conduits for vigorous air motion. The Megadunes site provides a possible modern analog for the glacial conditions in the Vostok, Dome Fuji, and Dome C ice core records and a possible explanation for lower-than-expected (15)N/(14)N ratios in trapped air bubbles at these times. A general conclusion is that very low accumulation rate causes deep air convection via its effect on firn structural characteristics. (C) 2010 Elsevier B.V. All rights reserved.

Rhodes, RH, Brook EJ, Chiang JCH, Blunier T, Maselli OJ, McConnell JR, Romanini D, Severinghaus JP.  2015.  Enhanced tropical methane production in response to iceberg discharge in the North Atlantic. Science. 348:1016-1019.   10.1126/science.1262005   AbstractWebsite

The causal mechanisms responsible for the abrupt climate changes of the Last Glacial Period remain unclear. One major difficulty is dating ice-rafted debris deposits associated with Heinrich events: Extensive iceberg influxes into the North Atlantic Ocean linked to global impacts on climate and biogeochemistry. In a new ice core record of atmospheric methane with ultrahigh temporal resolution, we find abrupt methane increases within Heinrich stadials 1, 2, 4, and 5 that, uniquely, have no counterparts in Greenland temperature proxies. Using a heuristic model of tropical rainfall distribution, we propose that Hudson Strait Heinrich events caused rainfall intensification over Southern Hemisphere land areas, thereby producing excess methane in tropical wetlands. Our findings suggest that the climatic impacts of Heinrich events persisted for 740 to 1520 years.

Severinghaus, JP, Keeling RF, Miller BR, Weiss RF, Deck B, Broecker WS.  1997.  Feasibility of using sand dunes as archives of old air. Journal of Geophysical Research-Atmospheres. 102:16783-16792.   10.1029/97jd00525   AbstractWebsite

Large unaltered samples of the atmosphere covering the past century would complement the history of atmospheric gases obtained from bubbles in ice cores, enabling measurement of geochemically important species such as O-2, (CH4)-C-14, and (CO)-C-14. Sand dunes are a porous media with interstitial air in diffusive contact with the atmosphere, somewhat analogous to the unconsolidated layer of firn atop glaciers. Recent studies have demonstrated the value of firn as an archive of old air [Battle et al., 1996; Bender et al., 1994a]. Unlike firn, sand dunes are incompressible and so remain permeable to greater depths and may extend the firn record into the past century. To evaluate the feasibility of using sand dunes as archives of old air, we drilled 60 m deep test holes in the Algodones Dunes, Imperial Valley, California. The main objective was to see if the air in a sand dune is as old as predicted by a diffusion model, or if the dune is rapidly flushed by advective pumping during windstorms and barometric pressure changes. We dated the air with chlorofluorocarbons and krypton-85, anthropogenic tracers whose atmospheric concentrations are known and have been increasing rapidly in the past half century. These tracer data match the pure diffusion model well, showing that advection in this dune is negligible compared to diffusion as a transport mechanism and that the mean age of the air at 61 m depth is similar to 10 years. Dunes therefore do contain old air. However, dunes appear to suffer from two serious drawbacks as archives. Microbial metabolism is evident in elevated CO2 and N2O and depressed CH4 and O-2 concentrations in this dune, corrupting the signals of interest in this and probably most dunes. Second, isotopic analyses of N-2 and O-2 from the dune show that fractionation of the gases occurs due to diffusion of water vapor, complicating the interpretation of the O-2 signal beyond the point of viability for an air archive. Sand dunes may be useful for relatively inert gases with large atmospheric concentration changes such as chlorofluorocarbons.

Buizert, C, Martinerie P, Petrenko VV, Severinghaus JP, Trudinger CM, Witrant E, Rosen JL, Orsi AJ, Rubino M, Etheridge DM, Steele LP, Hogan C, Laube JC, Sturges WT, Levchenko VA, Smith AM, Levin I, Conway TJ, Dlugokencky EJ, Lang PM, Kawamura K, Jenk TM, White JWC, Sowers T, Schwander J, Blunier T.  2012.  Gas transport in firn: multiple-tracer characterisation and model intercomparison for NEEM, Northern Greenland. Atmospheric Chemistry and Physics. 12:4259-4277.   10.5194/acp-12-4259-2012   AbstractWebsite

Air was sampled from the porous firn layer at the NEEM site in Northern Greenland. We use an ensemble of ten reference tracers of known atmospheric history to characterise the transport properties of the site. By analysing uncertainties in both data and the reference gas atmospheric histories, we can objectively assign weights to each of the gases used for the depth-diffusivity reconstruction. We define an objective root mean square criterion that is minimised in the model tuning procedure. Each tracer constrains the firn profile differently through its unique atmospheric history and free air diffusivity, making our multiple-tracer characterisation method a clear improvement over the commonly used single-tracer tuning. Six firn air transport models are tuned to the NEEM site; all models successfully reproduce the data within a 1 sigma Gaussian distribution. A comparison between two replicate boreholes drilled 64 m apart shows differences in measured mixing ratio profiles that exceed the experimental error. We find evidence that diffusivity does not vanish completely in the lock-in zone, as is commonly assumed. The ice age- gas age difference (Delta age) at the firn-ice transition is calculated to be 182(-9)(+3) yr. We further present the first intercomparison study of firn air models, where we introduce diagnostic scenarios designed to probe specific aspects of the model physics. Our results show that there are major differences in the way the models handle advective transport. Furthermore, diffusive fractionation of isotopes in the firn is poorly constrained by the models, which has consequences for attempts to reconstruct the isotopic composition of trace gases back in time using firn air and ice core records.

Buizert, C, Gkinis V, Severinghaus JP, He F, Lecavalier BS, Kindler P, Leuenberger M, Carlson AE, Vinther B, Masson-Delmotte V, White JWC, Liu ZY, Otto-Bliesner B, Brook EJ.  2014.  Greenland temperature response to climate forcing during the last deglaciation. Science. 345:1177-1180.   10.1126/science.1254961   AbstractWebsite

Greenland ice core water isotopic composition (delta O-18) provides detailed evidence for abrupt climate changes but is by itself insufficient for quantitative reconstruction of past temperatures and their spatial patterns. We investigate Greenland temperature evolution during the last deglaciation using independent reconstructions from three ice cores and simulations with a coupled ocean-atmosphere climate model. Contrary to the traditional delta O-18 interpretation, the Younger Dryas period was 4.5 degrees +/- 2 degrees C warmer than the Oldest Dryas, due to increased carbon dioxide forcing and summer insolation. The magnitude of abrupt temperature changes is larger in central Greenland (9 degrees to 14 degrees C) than in the northwest (5 degrees to 9 degrees C), fingerprinting a North Atlantic origin. Simulated changes in temperature seasonality closely track changes in the Atlantic overturning strength and support the hypothesis that abrupt climate change is mostly a winter phenomenon.

Severinghaus, JP, Macdonald KC.  1988.  High inside Corners at Ridge-Transform Intersections. Marine Geophysical Researches. 9:353-367.   10.1007/bf00315005   AbstractWebsite

A large topographic high commonly occurs near the intersection of a rifted spreading center and a transform fault. The high occurs at the inside of the 90° bend in the plate boundary, and is called the ‘high inside corner’, while the area across the spreading center, the ‘outside corner’, is often anomalously low. To better understand the origin of this topographic asymmetry, we examine topographic maps of 53 ridge-transform intersections. We conclude the following: (1) High inside corners occur at 41 out of 42 ridge-transform intersections at slow spreading ridges, and thus should be considered characteristic and persistent features of rifted slow spreading ridges. They are conspicuously absent at fast spreading ridges or at spreading centers that lack a rift valley. (2) High inside corners occur wherever an axial rift valley is present, and an approximate 1:1 correlation exists between the relief of the rift valley and the magnitude of the asymmetry. (3) Large high inside corners occur at both long and short transform offsets. (4) High inside corners at long offsets decay off-axis faster than predicted by the square root of age cooling model, precluding a thermalisostatic origin, but consistent with dynamic or flexural uplift models.These observations support the existing hypothesis that the asymmetry is due to the contrast in lithospheric coupling that occurs in the active transform versus the inactive fracture zone. Active faulting in the transform breaks the lithosphere along a high angle fault, permitting vertical movement of the inside corner block, whereas the inactive fracture zone forms a weld that couples the outside corner to the adjacent block, preventing it from rising. Large asymmetry at very short transform offsets appears to be caused by the added effect of a second uplift mechanism. Young lithosphere in the rift valley couples to the older plate, and when it leaves the rift valley it lifts the older plate with it. At very short offsets, this ‘coupled uplift’ acts upon the high inside corner; at long offsets, it may upwarp the older plate or its expression may be muted.

Taylor, KC, Mayewski PA, Alley RB, Brook EJ, Gow AJ, Grootes PM, Meese DA, Saltzman ES, Severinghaus JP, Twickler MS, White JWC, Whitlow S, Zielinski GA.  1997.  The Holocene Younger Dryas transition recorded at Summit, Greenland. Science. 278:825-827.   10.1126/science.278.5339.825   AbstractWebsite

Analysis of ice from Dye-3, Greenland, has demonstrated that the transition between the Younger Dryas and Holocene climate periods occurred over a 40-year period. A near annually resolved, multiparameter record of the transition recorded in the GISP2 core from Summit, Greenland, shows that most of the transition occurred in a series of steps with durations of about 5 years. Some climate proxies associated with more northern regions. Changes in atmospheric water vapor are likely to have played a large role in the climate transition.

Baggenstos, D, Severinghaus JP, Mulvaney R, McConnell JR, Sigl M, Maselli O, Petit JR, Grente B, Steig EJ.  2018.  A horizontal ice core from Taylor Glacier, its implications for Antarctic climate history, and an improved Taylor Dome ice core time scale. Paleoceanography and Paleoclimatology. 33:778-794.   10.1029/2017pa003297   AbstractWebsite

Ice core records from Antarctica show mostly synchronous temperature variations during the last deglacial transition, an indication that the climate of the entire continent reacted as one unit to the global changes. However, a record from the Taylor Dome ice core in the Ross Sea sector of East Antarctica has been suggested to show a rapid warming, similar in style and synchronous with the Oldest Dryas-Bolling warming in Greenland. Since publication of the Taylor Dome record, a number of lines of evidence have suggested that this interpretation is incorrect and reflects errors in the underlying time scale. The issues raised regarding the dating of Taylor Dome currently linger unresolved, and the original time scale remains the de facto chronology. We present new water isotope and chemistry data from nearby Taylor Glacier to resolve the confusion surrounding the Taylor Dome time scale. We find that the Taylor Glacier record is incompatible with the original interpretation of the Taylor Dome ice core, showing that the warming in the area was gradual and started at similar to 18 ka BP (before 1950) as seen in other East Antarctic ice cores. We build a consistent, up-to-date Taylor Dome chronology from 0 to 60 ka BP by combining new and old age markers based on synchronization to other ice core records. The most notable feature of the new TD2015 time scale is a gas age-ice age difference of up to 12,000 years during the Last Glacial Maximum, by far the largest ever observed.

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.

Schaefer, H, Petrenko VV, Brook EJ, Severinghaus JP, Reeh N, Melton JR, Mitchell L.  2009.  Ice stratigraphy at the Pakitsoq ice margin, West Greenland, derived from gas records. Journal of Glaciology. 55:411-421.   10.3189/002214309788816704   AbstractWebsite

Horizontal ice-core sites, where ancient ice is exposed at the glacier surface, offer unique opportunities for paleo-studies of trace components requiring large sample volumes. Following previous work at the Pakitsoq ice margin in West Greenland, we use a combination of geochemical parameters measured in the ice matrix (delta(18)O(ice)) and air occlusions (delta(18)O(atm), delta(15)N of N(2) and methane concentration) to date ice layers from specific climatic intervals. The data presented here expand our understanding of the stratigraphy and three-dimensional structure of ice layers outcropping at Pakitsoq. Sections containing ice from every distinct climatic interval during Termination I, including Last Glacial Maximum, Bolling/Allerod, Younger Dryas and the early Holocene, are identified. In the early Holocene, we find evidence for climatic fluctuations similar to signals found in deep ice cores from Greenland. A second glacial-interglacial transition exposed at the extreme margin of the ice is identified as another outcrop of Termination I (rather than the onset of the Eemian interglacial as postulated in earlier work). Consequently, the main structural feature at Pakitsoq is a large-scale anticline with accordion-type folding in both exposed sequences of the glacial-Holocene transition, leading to multiple layer duplications and age reversals.

Landais, A, Caillon N, Severinghaus J, Barnola JM, Goujon C, Jouzel J, Masson-Delmotte V.  2004.  Isotopic measurements of air trapped in ice to quantify temperature changes. Comptes Rendus Geoscience. 336:963-970.   10.1016/j.crte.2004.03.013   AbstractWebsite

Isotopic measurements of air trapped in ice to quantify temperature changes. Isotopic measurements in polar ice core have shown a succession of rapid warming periods during the last glacial period over Greenland. However, this method underestimates the surface temperature variations. A new method based on gas thermal diffusion in the firn manages to quantify surface temperature variations through associated isotopic fractionations. We developed a method to extract air from the ice and to perform isotopic measurements to reduce analytical uncertainties to 0.006 and 0.020parts per thousand for delta(15)N and delta(40)Ar. It led to a 16 +/- 1.5degreesC surface temperature variation during a rapid warming (-70000 yr). (C) 2004 Academie des sciences. Publie par Elsevier SAS. Tous droits reserves.

Petrenko, VV, Smith AM, Brailsford G, Riedel K, Hua Q, Lowe D, Severinghaus JP, Levchenko V, Bromley T, Moss R, Muhle J, Brook EJ.  2008.  A new method for analyzing (14)C of methane in ancient air extracted from glacial ice. Radiocarbon. 50:53-73. AbstractWebsite

We present a new method developed for measuring radiocarbon of methane ((14)CH(4)) in ancient air samples extracted from glacial ice and dating 11,000-15,000 calendar years before present. The small size (similar to 20 mu g CH(4) carbon), low CH(4) concentrations ([CH(4)], 400-800 parts per billion [ppb]), high carbon monoxide concentrations ([CO]), and low (14)C activity of the samples created unusually high risks of contamination by extraneous carbon. Up to 2500 ppb CO in the air samples was quantitatively removed using the Sofnocat reagent. (14)C procedural blanks were greatly reduced through the construction of a new CH(4) conversion line utilizing platinized quartz wool for CH(4) combustion and the use of an ultra-high-purity iron catalyst for graphitization. The amount and (14)C activity of extraneous carbon added in the new CH(4) conversion line were determined to be 0.23 +/- 0.16 pg and 23.57 +/- 16.22 pMC, respectively. The amount of modern (100 pMC) carbon added during the graphitization step has been reduced to 0.03 mu g. The overall procedural blank for all stages of sample handling was 0.75 0.38 pMC for similar to 20-mu g, (14)C-free air samples with [CH(4)] of 500 ppb. Duration of the graphitization reactions for small (<25 mu g C) samples was greatly reduced and reaction yields improved through more efficient water vapor trapping and the use of a new iron catalyst with higher surface area. (14)C corrections for each step of sample handling have been determined. The resulting overall (14)CH(4) uncertainties for the ancient air samples are similar to 1.0 pMC.

Arnold, T, Harth CM, Mühle J, Manning AJ, Salameh PK, Kim J, Ivy DJ, Steele PL, Petrenko VV, Severinghaus JP, Baggenstos D, Weiss RF.  2013.  Nitrogen trifluoride global emissions estimated from updated atmospheric measurements. Proceedings of the National Academy of Sciences.   10.1073/pnas.1212346110   AbstractWebsite

Nitrogen trifluoride (NF3) has potential to make a growing contribution to the Earth’s radiative budget; however, our understanding of its atmospheric burden and emission rates has been limited. Based on a revision of our previous calibration and using an expanded set of atmospheric measurements together with an atmospheric model and inverse method, we estimate that the global emissions of NF3 in 2011 were 1.18 ± 0.21 Gg⋅y−1, or ∼20 Tg CO2-eq⋅y−1 (carbon dioxide equivalent emissions based on a 100-y global warming potential of 16,600 for NF3). The 2011 global mean tropospheric dry air mole fraction was 0.86 ± 0.04 parts per trillion, resulting from an average emissions growth rate of 0.09 Gg⋅y−2 over the prior decade. In terms of CO2 equivalents, current NF3 emissions represent between 17% and 36% of the emissions of other long-lived fluorinated compounds from electronics manufacture. We also estimate that the emissions benefit of using NF3 over hexafluoroethane (C2F6) in electronics manufacture is significant—emissions of between 53 and 220 Tg CO2-eq⋅y−1 were avoided during 2011. Despite these savings, total NF3 emissions, currently ∼10% of production, are still significantly larger than expected assuming global implementation of ideal industrial practices. As such, there is a continuing need for improvements in NF3 emissions reduction strategies to keep pace with its increasing use and to slow its rising contribution to anthropogenic climate forcing.

Kawamura, K, Parrenin F, Lisiecki L, Uemura R, Vimeux F, Severinghaus JP, Hutterli MA, Nakazawa T, Aoki S, Jouzel J, Raymo ME, Matsumoto K, Nakata H, Motoyama H, Fujita S, Goto-Azuma K, Fujii Y, Watanabe O.  2007.  Northern Hemisphere forcing of climatic cycles in Antarctica over the past 360,000 years. Nature. 448:912-U4.   10.1038/nature06015   AbstractWebsite

The Milankovitch theory of climate change proposes that glacial interglacial cycles are driven by changes in summer insolation at high northern latitudes(1). The timing of climate change in the Southern Hemisphere at glacial-interglacial transitions (which are known as terminations) relative to variations in summer insolation in the Northern Hemisphere is an important test of this hypothesis. So far, it has only been possible to apply this test to the most recent termination(2,3), because the dating uncertainty associated with older terminations is too large to allow phase relationships to be determined. Here we present a new chronology of Antarctic climate change over the past 360,000 years that is based on the ratio of oxygen to nitrogen molecules in air trapped in the Dome Fuji and Vostok ice cores(4,5). This ratio is a proxy for local summer insolation(5), and thus allows the chronology to be constructed by orbital tuning without the need to assume a lag between a climate record and an orbital parameter. The accuracy of the chronology allows us to examine the phase relationships between climate records from the ice cores(6-9) and changes in insolation. Our results indicate that orbital-scale Antarctic climate change lags Northern Hemisphere insolation by a few millennia, and that the increases in Antarctic temperature and atmospheric carbon dioxide concentration during the last four terminations occurred within the rising phase of Northern Hemisphere summer insolation. These results support the Milankovitch theory that Northern Hemisphere summer insolation triggered the last four deglaciations(3,10,11).

Petrenko, VV, Severinghaus JP, Brook EJ, Muhle J, Headly M, Harth CM, Schaefer H, Reeh N, Weiss RF, Lowe D, Smith AM.  2008.  A novel method for obtaining very large ancient air samples from ablating glacial ice for analyses of methane radiocarbon. Journal of Glaciology. 54:233-244.   10.3189/002214308784886135   AbstractWebsite

We present techniques for obtaining large (similar to 100 L STP) samples of ancient air for analysis of (14)C of methane ((14)CH(4)) and other trace constituents. Paleoatmospheric (14)CH(4) measurements should constrain the fossil fraction of past methane budgets, as well as provide a definitive test of methane clathrate involvement in large and rapid methane concentration ([CH(4)]) increases that accompanied rapid warming events during the last deglaciation. Air dating to the Younger Dryas-Preboreal and Oldest Dryas-Bolling abrupt climatic transitions was obtained by melt extraction from old glacial ice outcropping at an ablation margin in West Greenland. The outcropping ice and occluded air were dated using a combination of delta(15)N of N(2), delta(18)O of O(2), delta(18)O(ice) and [CH(4)] measurements. The [CH(4)] blank of the melt extractions was <4 ppb. Measurements of delta(18)O and delta(15)N indicated no significant gas isotopic fractionation from handling. Measured Ar/N(2), CFC-11 and CFC-12 in the samples indicated no significant contamination from ambient air. Ar/N(2), Kr/Ar and Xe/Ar ratios in the samples were used to quantify effects of gas dissolution during the melt extractions and correct the sample [CH(4)]. Corrected [CH(4)] is elevated over expected values by up to 132 ppb for most samples, suggesting some in situ CH(4) production in ice at this site.

Mitchell, LE, Buizert C, Brook EJ, Breton DJ, Fegyveresi J, Baggenstos D, Orsi A, Severinghaus J, Alley RB, Albert M, Rhodes RH, McConnell JR, Sigl M, Maselli O, Gregory S, Ahn J.  2015.  Observing and modeling the influence of layering on bubble trapping in polar firn. Journal of Geophysical Research-Atmospheres. 120:2558-2574.   10.1002/2014jd022766   AbstractWebsite

Interpretation of ice core trace gas records depends on an accurate understanding of the processes that smooth the atmospheric signal in the firn. Much work has been done to understand the processes affecting air transport in the open pores of the firn, but a paucity of data from air trapped in bubbles in the firn-ice transition region has limited the ability to constrain the effect of bubble closure processes. Here we present high-resolution measurements of firn density, methane concentrations, nitrogen isotopes, and total air content that show layering in the firn-ice transition region at the West Antarctic Ice Sheet (WAIS) Divide ice core site. Using the notion that bubble trapping is a stochastic process, we derive a new parameterization for closed porosity that incorporates the effects of layering in a steady state firn modeling approach. We include the process of bubble trapping into an open-porosity firn air transport model and obtain a good fit to the firn core data. We find that layering broadens the depth range over which bubbles are trapped, widens the modeled gas age distribution of air in closed bubbles, reduces the mean gas age of air in closed bubbles, and introduces stratigraphic irregularities in the gas age scale that have a peak-to-peak variability of 10 years at WAIS Divide. For a more complete understanding of gas occlusion and its impact on ice core records, we suggest that this experiment be repeated at sites climatically different from WAIS Divide, for example, on the East Antarctic plateau.

Fudge, TJ, Steig EJ, Markle BR, Schoenemann SW, Ding QH, Taylor KC, McConnell JR, Brook EJ, Sowers T, White JWC, Alley RB, Cheng H, Clow GD, Cole-Dai J, Conway H, Cuffey KM, Edwards JS, Edwards RL, Edwards R, Fegyveresi JM, Ferris D, Fitzpatrick JJ, Johnson J, Hargreaves G, Lee JE, Maselli OJ, Mason W, McGwire KC, Mitchell LE, Mortensen N, Neff P, Orsi AJ, Popp TJ, Schauer AJ, Severinghaus JP, Sigl M, Spencer MK, Vaughn BH, Voigt DE, Waddington ED, Wang XF, Wong GJ, Members WDP.  2013.  Onset of deglacial warming in West Antarctica driven by local orbital forcing. Nature. 500:440-+.   10.1038/nature12376   AbstractWebsite

The cause of warming in the Southern Hemisphere during the most recent deglaciation remains a matter of debate(1,2). Hypotheses for a Northern Hemisphere trigger, through oceanic redistributions of heat, are based in part on the abrupt onset of warming seen in East Antarctic ice cores and dated to 18,000 years ago, which is several thousand years after high-latitude Northern Hemisphere summer insolation intensity began increasing from its minimum, approximately 24,000 years ago(3,4). An alternative explanation is that local solar insolation changes cause the Southern Hemisphere to warm independently(2,5). Here we present results from a new, annually resolved ice-core record from West Antarctica that reconciles these two views. The records show that 18,000 years ago snow accumulation in West Antarctica began increasing, coincident with increasing carbon dioxide concentrations, warming in East Antarctica and cooling in the Northern Hemisphere(6) associated with an abrupt decrease in Atlantic meridional overturning circulation(7). However, significant warming in West Antarctica began at least 2,000 years earlier. Circum-Antarctic sea-ice decline, driven by increasing local insolation, is the likely cause of this warming. The marine-influenced West Antarctic records suggest a more active role for the Southern Ocean in the onset of deglaciation than is inferred from ice cores in the East Antarctic interior, which are largely isolated from sea-ice changes.