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Wagner, TJW, Dell RW, Eisenman I, Keeling RF, Padman L, Severinghaus JP.  2018.  Wave inhibition by sea ice enables trans-Atlantic ice rafting of debris during Heinrich events. Earth and Planetary Science Letters. 495:157-163.   10.1016/j.epsl.2018.05.006   AbstractWebsite

The last glacial period was punctuated by episodes of massive iceberg calving from the Laurentide Ice Sheet, called Heinrich events, which are identified by layers of ice-rafted debris (IRD) in ocean sediment cores from the North Atlantic. The thickness of these IRD layers declines more gradually with distance from the iceberg sources than would be expected based on present-day iceberg drift and decay. Here we model icebergs as passive Lagrangian particles driven by ocean currents, winds, and sea surface temperatures. The icebergs are released in a comprehensive climate model simulation of the last glacial maximum (LGM), as well as a simulation of the modern climate. The two simulated climates result in qualitatively similar distributions of iceberg meltwater and hence debris, with the colder temperatures of the LGM having only a relatively small effect on meltwater spread. In both scenarios, meltwater flux falls off rapidly with zonal distance from the source, in contrast with the more uniform spread of IRD in sediment cores. To address this discrepancy, we propose a physical mechanism that could have prolonged the lifetime of icebergs during Heinrich events. The mechanism involves a surface layer of cold and fresh meltwater formed from, and retained around, large densely packed armadas of icebergs. This leads to wintertime sea ice formation even in relatively low latitudes. The sea ice in turn shields the icebergs from wave erosion, which is the main source of iceberg ablation. We find that sea ice could plausibly have formed around the icebergs during four months each winter. Allowing for four months of sea ice in the model results in a simulated IRD distribution which approximately agrees with the distribution of IRD in sediment cores. (C) 2018 Elsevier B.V. All rights reserved.

Resplandy, L, Keeling RF, Stephens BB, Bent JD, Jacobson A, Rodenbeck C, Khatiwala S.  2016.  Constraints on oceanic meridional heat transport from combined measurements of oxygen and carbon. Climate Dynamics. 47:3335-3357.   10.1007/s00382-016-3029-3   AbstractWebsite

Despite its importance to the climate system, the ocean meridional heat transport is still poorly quantified. We identify a strong link between the northern hemisphere deficit in atmospheric potential oxygen (APO = O + 1.1 CO) and the asymmetry in meridional heat transport between northern and southern hemispheres. The recent aircraft observations from the HIPPO campaign reveal a northern APO deficit in the tropospheric column of 10.4 1.0 per meg, double the value at the surface and more representative of large-scale air-sea fluxes. The global northward ocean heat transport asymmetry necessary to explain the observed APO deficit is about 0.7-1.1 PW, which corresponds to the upper range of estimates from hydrographic sections and atmospheric reanalyses.

Tanhua, T, Keeling RF.  2012.  Changes in column inventories of carbon and oxygen in the Atlantic Ocean. Biogeosciences. 9:4819-4833.   10.5194/bg-9-4819-2012   AbstractWebsite

Increasing concentrations of dissolved inorganic carbon (DIC) in the interior ocean are expected as a direct consequence of increasing concentrations of CO2 in the atmosphere. This extra DIC is often referred to as anthropogenic carbon (C-ant), and its inventory, or increase rate, in the interior ocean has previously been estimated by a multitude of observational approaches. Each of these methods is associated with hard to test assumptions since C-ant cannot be directly observed. Results from a simpler concept with fewer assumptions applied to the Atlantic Ocean are reported on here using two large data collections of carbon relevant bottle data. The change in column inventory on decadal time scales, i.e. the storage rate, of DIC, respiration compensated DIC and oxygen is calculated for the Atlantic Ocean. We report storage rates and the confidence intervals of the mean trend at the 95% level (CI), reflecting the mean trend but not considering potential biasing effects of the spatial and temporal sampling. For the whole Atlantic Ocean the mean trends for DIC and oxygen are non-zero at the 95% confidence level: DIC: 0.86 (CI: 0.72-1.00) and oxygen: -0.24 (CI: -0.41-(-0.07)) mol m(-2) yr(-1). For oxygen, the whole Atlantic trend is dominated by the subpolar North Atlantic, whereas for other regions the O-2 trends are not significant. The storage rates are similar to changes found by other studies, although with large uncertainty. For the subpolar North Atlantic the storage rates show significant temporal and regional variation of all variables. This seems to be due to variations in the prevalence of subsurface water masses with different DIC and oxygen concentrations leading to sometimes different signs of storage rates for DIC compared to published C-ant estimates. This study suggest that accurate assessment of the uptake of CO2 by the oceans will require accounting not only for processes that influence C-ant but also additional processes that modify CO2 storage.

Keeling, RF, Garcia HE.  2002.  The change in oceanic O2 inventory associated with recent global warming. Proceedings of the National Academy of Sciences of the United States of America. 99:7848-7853.   10.1073/pnas.122154899   AbstractWebsite

Oceans general circulation models predict that global warming may cause a decrease in the oceanic O-2 inventory and an associated O-2 outgassing. An independent argument is presented here in support of this prediction based on observational evidence of the ocean's biogeochemical response to natural warming. On time scales from seasonal to centennial, natural O-2 flux/heat flux ratios are shown to occur in a range of 2 to 10 nmol of O-2 per joule of warming, with larger ratios typically occurring at higher latitudes and overlongertime scales. The ratios are several times larger than would be expected solely from the effect of heating on the O-2 solubility, indicating that most of the O-2 exchange is biologically mediated through links between heating and stratification. The change in oceanic O-2 inventory through the 1990s is estimated to be 0.3 +/- 0.4 X 10(14) mol of O-2 per year based on scaling the observed anomalous long-term ocean warming by natural O-2 flux/heating ratios and allowing for uncertainty due to decadal variability. Implications are discussed for carbon budgets based on observed changes in atmospheric O-2/N-2 ratio and based on observed changes in ocean dissolved inorganic carbon.

Keeling, RF, Stephens BB.  2001.  Antarctic sea ice and the control of Pleistocene climate instability (vol 16, pg 112, 2001). Paleoceanography. 16:330-334.   10.1029/2001pa000648   AbstractWebsite

In the paper “Antarctic sea ice and the control of Pleistocene climate instability” by Ralph F. Keeling and Britton B. Stephens (Paleoceanography, 16(1), 112-131,2001), approximately 10 paragraphs from section 5 and Appendix A were inadvertently omitted. The end of the paper from section 5 through the references, including Appendix A and Figure A1, appear below.

Keeling, RF, Stephens BB.  2001.  Antarctic sea ice and the control of Pleistocene climate instability. Paleoceanography. 16:112-131,330-334.   10.1029/2000pa000529   Abstract

A hypothesis is presented for the origin of Pleistocene climate instability, based on expansion of Antarctic sea ice and associated changes in the oceans' salinity structure. The hypothesis assumes that thermohaline overturning is dominated by the reconfigured conveyor of Toggweiler and Samuels [1993b], in which deepwater upwelling is restricted to high southern latitudes. The reconfigured conveyor is shown to be potentially stabilized in an "on" mode by precipitation at high southern latitudes and potentially destabilized into "on" and "off" modes by the counteracting influence of Antarctic sea ice. The mechanism is clarified by the use of a hydraulic analogue. We hypothesize that this mechanism accounts for dominant patterns of thermohaline overturning and climate instability between Pleistocene warm and cold periods. The hypothesis is shown to be consistent with a range of paleoceanographic evidence and to potentially account for details of observed rapid climate changes during glacial and interglacial periods, including aspects of interhemispheric timing.

Najjar, RG, Keeling RF.  2000.  Mean annual cycle of the air-sea oxygen flux: A global view. Global Biogeochemical Cycles. 14:573-584.   10.1029/1999gb900086   AbstractWebsite

A global monthly-mean climatology of the air-sea oxygen flux is presented and discussed. The climatology is based on the ocean oxygen climatology of Najjar and Keeling [1997] and wind speeds derived from a meteorological analysis center. Seasonal variations are characterized by outgassing of oxygen during spring and summer and ingassing of oxygen during fall and winter, a pattern consistent with thermal and biological forcing of the air-sea oxygen flux. The annual mean flux pattern is characterized by ingassing at high latitudes and the tropics and outgassing in middle latitudes. The air-sea oxygen flux is shown to exhibit patterns that agree well with patterns seen in a marine primary productivity climatology, in model generated air-sea O-2 fluxes, in estimates of remineralization in the shallow aphotic zone based on seasonal oxygen variations, in observed seasonal nutrient-temperature relationships, and in independent estimates of meridional oxygen transport in the Atlantic ocean. We also find that extratropical mixed layer new production during the spring-summer period, computed from biological seasonal net outgassing of oxygen, is equivalent to the production of 4.5-5.6 Gt C, much lower than previous estimates based on atmospheric O-2/N-2 measurements.

Stephens, BB, Keeling RF, Heimann M, Six KD, Murnane R, Caldeira K.  1998.  Testing global ocean carbon cycle models using measurements of atmospheric O2 and CO2 concentration. Global Biogeochemical Cycles. 12:213-230.   10.1029/97gb03500   AbstractWebsite

We present a method for testing the performance of global ocean carbon cycle models using measurements of atmospheric O-2 and CO2 concentration. We combine these measurements to define a tracer, atmospheric potential oxygen (APO approximate to O-2 + CO2), which is conservative with respect to terrestrial photosynthesis and respiration. We then compare observations of APO to the simulations of an atmospheric transport model which uses ocean-model air-sea fluxes and fossil fuel combustion estimates as lower boundary conditions. We present observations of the annual-average concentrations of CO2, O-2, and APO at 10 stations in a north-south transect. The observations of APO show a significant interhemispheric gradient decreasing towards the north. We use air-sea CO2, O-2, and N-2 fluxes from the Princeton ocean biogeochemistry model, the Hamburg model of the ocean carbon cycle, and the Lawrence Livermore ocean biogeochemistry model to drive the TM2 atmospheric transport model. The latitudinal variations in annual-average APO predicted by the combined models are distinctly different from the observations. All three models significantly underestimate the interhemispheric difference in APO, suggesting that they underestimate the net southward transport of the sum of O-2 and CO2 in the oceans. Uncertainties in the model-observation comparisons include uncertainties associated with the atmospheric measurements, the atmospheric transport model, and the physical and biological components of the ocean models. Potential deficiencies in the physical components of the ocean models, which have previously been suggested as causes for anomalously large heat fluxes out of the Southern Ocean, may contribute to the discrepancies with the APO observations. These deficiencies include the inadequate parameterization of subgrid-scale isopycnal eddy mixing, a lack of subgrid-scale vertical convection, too much Antarctic sea-ice formation, and an overestimation of vertical diffusivities in the main thermocline.