Bibliography - E. D. Galbraith
- Galbraith, E. D., E. Y. Kwon, A. Gnanadesikan, K. B. Rodgers, Stephen M. Griffies, D. Bianchi, Jorge Sarmiento, J. P. Dunne, J. Simeon, R. D. Slater, Andrew T. Wittenberg, and I. Held, 2011: Climate Variability and Radiocarbon in the CM2Mc Earth System Model. Journal of Climate, American Meteorological Society, doi:10.1175/2011JCLI3919.1
[ Abstract ]The distribution of radiocarbon (14C) in the ocean and atmosphere has fluctuated on timescales ranging from seasons to millennia. It is thought that these fluctuations partly reflect variability in the climate system, offering a rich potential source of information to help understand mechanisms of past climate change. Here, a long simulation with a new, coupled model is used to explore the mechanisms that redistribute 14C within the Earth system on inter-annual to centennial timescales. The model, CM2Mc, is a lower-resolution version of the Geophysical Fluid Dynamics Laboratory's CM2M model, uses no flux adjustments, and incorporates a simple prognostic ocean biogeochemistry model including 14C. The atmospheric 14C and radiative boundary conditions are held constant, so that the oceanic distribution of 14C is only a function of internal climate variability. The simulation displays previously-described relationships between tropical sea surface 14C and the model-equivalents of the El Niño Southern Oscillation and Indonesian Throughflow. Sea surface 14C variability also arises from fluctuations in the circulations of the subarctic Pacific and Southern Ocean, including North Pacific decadal variability, and episodic ventilation events in the Weddell Sea that are reminiscent of the Weddell Polynya of 1974-1976. Interannual variability in the air-sea balance of 14C is dominated by exchange within the belt of intense Southern Westerly winds, rather than at the convective locations where the surface 14C is most variable. Despite significant interannual variability, the simulated impact on air-sea exchange is an order of magnitude smaller than the recorded atmospheric 14C variability of the past millennium. This result partly reflects the importance of variability in the production rate of 14C in determining atmospheric 14C, but may also reflect an underestimate of natural climate variability, particularly in the Southern Westerly winds.
- Rodgers, K. B., S. E. Mikaloff-Fletcher, D. Bianchi, C. Beaulieu, E. D. Galbraith, A. Gnanadesikan, A. G. Hogg, D. Iudicone, B. R. Lintner, T. Naegler, P. J. Reimer, Jorge Sarmiento, and R. D. Slater, 2011: Interhemispheric gradient of atmospheric radiocarbon reveals natural variability of Southern Ocean winds. Climate of the Past, European Geosciences Union, 7, doi:10.5194/cp-7-1123-2011 1123-1138
[ Abstract ]Tree ring Δ14C data (Reimer et al., 2004; McCormac et al., 2004) indicate that atmospheric Δ14C varied on
multi-decadal to centennial timescales, in both hemispheres, over the period between AD950 and 1830. The Northern and Southern Hemispheric Δ14C records display similar variability, but from the data alone is it not clear whether these variations are driven by the production of 14C in the stratosphere (Stuiver and Quay, 1980) or by perturbations to exchanges
between carbon reservoirs (Siegenthaler et al., 1980). As the sea-air flux of 14CO2 has a clear maximum in the open ocean regions of the Southern Ocean, relatively modest perturbations to the winds over this region drive significant perturbations
to the interhemispheric gradient. In this study, model
simulations are used to show that Southern Ocean winds are likely a main driver of the observed variability in the interhemispheric gradient over AD950-1830, and further, that this variability may be larger than the Southern Ocean wind trends that have been reported for recent decades (notably 1980-2004). This interpretation also implies that there may have been a significant weakening of the winds over the Southern Ocean within a few decades of AD1375, associated
with the transition between the Medieval Climate Anomaly and the Little Ice Age. The driving forces that could have produced such a shift in the winds at the Medieval Climate Anomaly to Little Ice Age transition remain unknown. Our process-focused suite of perturbation experiments with models raises the possibility that the current generation of coupled
climate and earth system models may underestimate the natural background multi-decadal- to centennial-timescale variations in the winds over the Southern Ocean.
- Jaccard, S. L., E. D. Galbraith, Daniel Sigman, and G. H. Haug, 2010: A pervasive link between Antarctic ice core and subarctic Pacific sediment records over the past 800 kyrs. Quaternary Science Reviews, 29, doi:10.1016/j.quascirev.2009.10.007 206-212
[ Abstract ]Recently developed XRF core-scanning methods permit paleoceanographic reconstructions on timescales similar to those of ice-core records. We have investigated the distribution of biogenic barium (Ba/Al), opal and carbonate (Ca/Al) in a sediment core retrieved from the abyssal subarctic Pacific (ODP 882,
50°N, 167°E, 3244 m) over an interval that spans the full length of the EPICA Dome C (EDC) ice-core record. Ba/Al and biogenic opal show a strong resemblance to the EDC δD and CO2, with generally high
concentrations during interglacials and lower values during ice ages of the past 800 kyrs. The sedimentary
Ba/Al and biogenic opal are most easily interpreted as indicating a reduced sinking flux of
organic matter from the surface ocean during cold periods. The Ba/Al maxima during peak interglacials
are accompanied by transient Ca/Al peaks in these otherwise carbonate-devoid sediments, which are
best explained by a deepening of the calcite lysocline, presumably due to reduced storage of respired CO2 in the deep North Pacific. For most of the ‘‘luke-warm’’ interglacials noted between 420 and 750 ka in
EDC, the Ba/Al peaks in ODP 882 are also lower, further strengthening the evidence for a simple physical
link between global climate and the biogeochemistry of the subarctic Pacific.
- Jaccard, S. L., E. D. Galbraith, Daniel Sigman, G. H. Haug, R. Francois, T. F. Pedersen, P. Dulski, and H. R. Thierstein, 2009: Subarctic Pacific evidence for a glacial deepening of the oceanic respired carbon pool. Earth and Planetary Science Letters, 277, doi:10.1016/j.epsl.2008.10.017 156-165
[ Abstract ]Measurements of benthic foraminiferal cadmium: calcium (Cd/Ca) have indicated that the
glacial–interglacial change in deep North Pacific phosphate (PO4) concentration was
minimal, which has been taken by some workers as a sign that the biological pump did not
store more carbon in the deep glacial ocean. Here we present sedimentary redoxsensitive
trace metal records from Ocean Drilling Program (ODP) Site 882 (NW subarctic Pacific,
water depth 3244 m) to make inferences about changes in deep North Pacific oxygenation –
and thus respired carbon storage – over the past 150,000 yr. These observations are
complemented with biogenic barium and opal measurements as indicators for past organic
carbon export to separate the influences of deepwater
oxygen concentration and
sedimentary organic carbon respiration on the redox state of the sediment. Our results
suggest that the deep subarctic Pacific water mass was depleted in oxygen during glacial
maxima, though it was not anoxic. We reconcile our results with the existing benthic
foraminiferal Cd/Ca by invoking a decrease in the fraction of the deep ocean nutrient
inventory that was preformed, rather than remineralized. This change would have
corresponded to an increase in the deep Pacific storage of respired carbon, which would
have lowered atmospheric carbon dioxide (CO2) by sequestering CO2 away from the
atmosphere and by increasing ocean alkalinity through a transient dissolution event in the
deep sea. The magnitude of change in preformed nutrients suggested by the North Pacific
data would have accounted for a majority of the observed decrease in glacial atmospheric
pCO2.
- Galbraith, E. D., S. L. Jaccard, T. F. Pedersen, Daniel Sigman, G. H. Haug, M. S. Cook, J. R. Southon, and R. Francois, 2007: Carbon dioxide release from the North Pacific abyss during the last deglaciation. Nature, doi:10.1038/nature06227 890-893
[ Abstract ]Atmospheric carbon dioxide concentrations were significantly lower during glacial
periods than during intervening interglacial periods, but the mechanisms responsible for
this difference remain uncertain. Many recent explanations call on greater carbon storage
in a poorly ventilated deep ocean during glacial periods, but direct evidence regarding
the ventilation and respired carbon content of the glacial deep ocean is sparse and often
equivocal. Here we present sedimentary geochemical records from sites spanning the
deep subarctic Pacific that - together with previously published results - show that a
poorly ventilated water mass containing a high concentration of respired carbon dioxide
occupied the North Pacific abyss during the Last Glacial Maximum. Despite an inferred
increase in deep Southern Ocean ventilation during the first step of the deglaciation
(18,000–15,000 years ago), we find no evidence for improved ventilation in the
abyssal subarctic Pacific until a rapid transition 14,600 years ago: this change was
accompanied by an acceleration of export production from the surface waters above but
only a small increase in atmospheric carbon dioxide concentration. We speculate that
these changes were mechanistically linked to a roughly coeval increase in deep water
formation in the North Atlantic, which flushed respired carbon dioxide from northern
abyssal waters, but also increased the supply of nutrients to the upper ocean, leading to
greater carbon dioxide sequestration at mid-depths and stalling the rise of atmospheric
carbon dioxide concentrations. Our findings are qualitatively consistent with hypotheses
invoking a deglacial flushing of respired carbon dioxide from an isolated, deep ocean
reservoir, but suggest that the reservoir may have been released in stages, as
vigorous deep water ventilation switched between North Atlantic and Southern Ocean
source regions.
Direct link to page: http://cmi.princeton.edu/bibliography/results.php?author=3698