Adam E. Scrivner

Testing the extraction of past seawater Nd isotopic composition from North Atlantic deep sea sediments and foraminifera.

Neodymium isotopes provide a paleoceanographic proxy for past deep water circulation and local weathering changes and have been measured on various authigenic marine sediment components, including fish teeth, ferromanganese oxides extracted by acid-reductive leaching, cleaned foraminifera, and foraminifera with Fe-Mn oxide coatings. Here we compare Nd isotopic measurements obtained from ferromanganese oxides leached from bulk sediments and planktonic foraminifera, as well as from oxidatively-reductively cleaned foraminiferal shells from sediment cores in the North Atlantic. Sedimentary volcanic ash contributes a significant fraction of the Nd when the ferro-manganese (Fe-Mn) oxide coatings are leached from bulk sediments. Reductive leachates of marine sediments from North Atlantic core tops near Iceland, or directly downstream from Iceland-Scotland Overflow Waters, record ɛNd values that are significantly higher than seawater, indicating that volcanic material is easily leached by acid-reductive methods. The ɛNd values from sites more distal to Iceland are similar to modern seawater values, showing little contamination from Iceland-derived volcanogenic material. In all comparisons, core top planktonic foraminifera ɛNd values more closely approximate modern deep seawater than the bulk sediment reductive leached value suggesting that the foraminifera provide a route toward quantifying the Nd isotopic signature of deep North Atlantic water masses.

Radiocarbon evidence for alternating northern and southern sources of ventilation of the deep Atlantic carbon pool during the last deglaciation

Significance This study sheds light on the mechanisms of deglacial atmospheric CO2 rise and, more specifically, on the hypothesized role of a “bipolar seesaw” in deep Atlantic ventilation. Comparing new high-resolution radiocarbon reconstructions from the Northeast Atlantic with existing data from the Southern Ocean, we show that a bipolar ventilation seesaw did indeed operate during the last deglaciation. Whereas today the deep Atlantic’s carbon pool is “flushed” from the north by North Atlantic Deep Water export, it was flushed instead from the south during Heinrich Stadial 1 and the Younger Dryas, in time with sustained atmospheric CO2 rise. Recent theories for glacial–interglacial climate transitions call on millennial climate perturbations that purged the deep sea of sequestered carbon dioxide via a “bipolar ventilation seesaw.” However, the viability of this hypothesis has been contested, and robust evidence in its support is lacking. Here we present a record of North Atlantic deep-water radiocarbon ventilation, which we compare with similar data from the Southern Ocean. A striking coherence in ventilation changes is found, with extremely high ventilation ages prevailing across the deep Atlantic during the last glacial period. The data also reveal two reversals in the ventilation gradient between the deep North Atlantic and Southern Ocean during Heinrich Stadial 1 and the Younger Dryas. These coincided with periods of sustained atmospheric CO2 rise and appear to have been driven by enhanced ocean–atmosphere exchange, primarily in the Southern Ocean. These results confirm the operation of a bipolar ventilation seesaw during deglaciation and underline the contribution of abrupt regional climate anomalies to longer-term global climate transitions.

North Atlantic versus Southern Ocean contributions to a deglacial surge in deep ocean ventilation

Past glacial-interglacial climate transitions were accompanied by millennial-scale pulses in atmospheric CO2 that are widely thought to have resulted from the release of CO2 via the Southern Ocean. However, direct proxy evidence for a Southern Ocean role in regulating past ocean-atmosphere CO2 exchange is scarce. Here we use combined radiocarbon and neodymium isotope measurements from the last deglaciation to confirm greatly enhanced overturning and/or air-sea exchange rates relative to today, in particular during the Bolling-Allerod warm interval. We show that this deglacial pulse in ocean ventilation was not driven by the North Atlantic overturning alone, and must have involved an increase in the ventilation of southern-sourced deep waters. Our results thus confirm the removal of a physical and/or dynamical barrier to effective air-sea (CO2) exchange in the Southern Ocean during deglaciation, and highlight the Antarctic region as a key locus for global climate/carbon-cycle feedbacks.

Radiocarbon constraints on the glacial ocean circulation and its impact on atmospheric CO2

While the ocean’s large-scale overturning circulation is thought to have been significantly different under the climatic conditions of the Last Glacial Maximum (LGM), the exact nature of the glacial circulation and its implications for global carbon cycling continue to be debated. Here we use a global array of ocean–atmosphere radiocarbon disequilibrium estimates to demonstrate a ∼689±53 14C-yr increase in the average residence time of carbon in the deep ocean at the LGM. A predominantly southern-sourced abyssal overturning limb that was more isolated from its shallower northern counterparts is interpreted to have extended from the Southern Ocean, producing a widespread radiocarbon age maximum at mid-depths and depriving the deep ocean of a fast escape route for accumulating respired carbon. While the exact magnitude of the resulting carbon cycle impacts remains to be confirmed, the radiocarbon data suggest an increase in the efficiency of the biological carbon pump that could have accounted for as much as half of the glacial–interglacial CO2 change.

Graphitization of Small Carbonate Samples for Paleoceanographic Research at the Godwin Radiocarbon Laboratory, University of Cambridge

A new radiocarbon preparation facility was set up in 2010 at the Godwin Laboratory for Palaeoclimate Research, at the University of Cambridge. Samples are graphitized via hydrogen reduction on an iron powder catalyst before being sent to the Chrono Centre, Belfast, or the Australian National University for accelerator mass spectrometry (AMS) analysis. The experimental set-up and procedure have recently been developed to investigate the potential for running small samples of foraminiferal carbonate. By analysing background values of samples ranging from 0.04-0.6mgC along with similar sized secondary standards, the set-up and experimental procedures were optimised for small samples. ‘Background’ modern radiocarbon contamination has been minimised through careful selection of iron powder, and graphitization has been optimised through the use of ‘small volume’ reactors, allowing samples containing as little as 0.08mgC to be graphitized and accurately dated. Graphitization efficiency/fractionation is found not to be the main limitation on the analysis of samples smaller than 0.07mgC, which rather depends primarily on AMS ion beam optics, suggesting further improvements in small sample analysis might yet be achieved with our methodology.