Morten B. Andersen

Strong and deep Atlantic meridional overturning circulation during the last glacial cycle

Extreme, abrupt Northern Hemisphere climate oscillations during the last glacial cycle (140,000 years ago to present) were modulated by changes in ocean circulation and atmospheric forcing. However, the variability of the Atlantic meridional overturning circulation (AMOC), which has a role in controlling heat transport from low to high latitudes and in ocean CO2 storage, is still poorly constrained beyond the Last Glacial Maximum. Here we show that a deep and vigorous overturning circulation mode has persisted for most of the last glacial cycle, dominating ocean circulation in the Atlantic, whereas a shallower glacial mode with southern-sourced waters filling the deep western North Atlantic prevailed during glacial maxima. Our results are based on a reconstruction of both the strength and the direction of the AMOC during the last glacial cycle from a highly resolved marine sedimentary record in the deep western North Atlantic. Parallel measurements of two independent chemical water tracers (the isotope ratios of 231Pa/230Th and 143Nd/144Nd), which are not directly affected by changes in the global cycle, reveal consistent responses of the AMOC during the last two glacial terminations. Any significant deviations from this configuration, resulting in slowdowns of the AMOC, were restricted to centennial-scale excursions during catastrophic iceberg discharges of the Heinrich stadials. Severe and multicentennial weakening of North Atlantic Deep Water formation occurred only during Heinrich stadials close to glacial maxima with increased ice coverage, probably as a result of increased fresh-water input. In contrast, the AMOC was relatively insensitive to submillennial meltwater pulses during warmer climate states, and an active AMOC prevailed during Dansgaard–Oeschger interstadials (Greenland warm periods).

Precise determination of the open ocean 234U/238U composition

Uranium has a long residence time in the open oceans, and therefore, its salinity-normalized U concentration and 234U/238U activity ratio (expressed herein as δ234U, the ‰ deviation from secular equilibrium) are assumed to be uniform. The marine 234U/238U activity ratio is currently in radioactive disequilibrium and shows a ∼15% excess of 234U with respect to the secular equilibrium value due to continuous input from riverine sources. Knowledge of the marine δ234U, and how it has evolved through the Quaternary, is important for validating age accuracy in the U series dating of marine carbonates, which is increasingly relied upon for providing a chronological basis in paleoclimate research. However, accurate and precise measurements of δ234U are technically difficult. Thus, existing compilations of the open ocean δ234U value vary by up to ∼10‰, and the assumed uniformity in the oceanic δ234U remains to be confirmed. Using MC-ICPMS techniques and a suite of multiple Faraday cups instead of the typical configurations based on a combined Faraday cup–multiplier array, a long-term reproducibility of better than ±0.3‰ (2σ) is achieved for δ234U measurements. Applying these very high precision techniques to open ocean seawater samples, an average δ234U of 146.8 ± 0.1‰ (2σm, n = 19) is obtained. These high-precision seawater measurements yield an external reproducibility of better than ±0.4‰ (2σ) and show that the open oceans have a uniform δ234U on the sub-‰ level. These new data constrain the vertical mixing time of the open oceans to less than 1000 years.

The oceanic budgets of nickel and zinc isotopes: the importance of sulfidic environments as illustrated by the Black Sea

Isotopic data collected to date as part of the GEOTRACES and other programmes show that the oceanic dissolved pool is isotopically heavy relative to the inputs for zinc (Zn) and nickel (Ni). All Zn sinks measured until recently, and the only output yet measured for Ni, are isotopically heavier than the dissolved pool. This would require either a non-steady-state ocean or other unidentified sinks. Recently, isotopically light Zn has been measured in organic carbon-rich sediments from productive upwelling margins, providing a potential resolution of this issue, at least for Zn. However, the origin of the isotopically light sedimentary Zn signal is uncertain. Cellular uptake of isotopically light Zn followed by transfer to sediment does not appear to be a quantitatively important process. Here, we present Zn and Ni isotope data for the water column and sediments of the Black Sea. These data demonstrate that isotopically light Zn and Ni are extracted from the water column, probably through an equilibrium fractionation between different dissolved species followed by sequestration of light Zn and Ni in sulfide species to particulates and the sediment. We suggest that a similar, non-quantitative, process, operating in porewaters, explains the Zn data from organic carbon-rich sediments. This article is part of the themed issue ‘Biological and climatic impacts of ocean trace element chemistry’.

Ocean mixing and ice-sheet control of seawater 234U/238U during the last deglaciation.

Uranium in the deep sea The ratio of 234U to 238U in seawater underlies modern marine uranium-thorium geochronology, but it is difficult to establish the ratio precisely. Chen et al. report two 234U/238U records derived from deep-sea corals (see the Perspective by Yokoyama and Esat). The records reveal a number of important similarities to and differences from existing records of the past 30,000 years. Higher values during the most recent 10,000 years than during earlier glaciated conditions may reflect enhanced subglacial melting during deglaciation. Science, this issue p. 626; see also p. 550 The 234U/238U ratios of deep-sea corals illuminate glacially driven changes of the past 30,000 years. Seawater 234U/238U provides global-scale information about continental weathering and is vital for marine uranium-series geochronology. Existing evidence supports an increase in 234U/238U since the last glacial period, but the timing and amplitude of its variability has been poorly constrained. Here we report two seawater 234U/238U records based on well-preserved deep-sea corals from the low-latitude Atlantic and Pacific Oceans. The Atlantic 234U/238U started to increase before major sea-level rise and overshot the modern value by 3 per mil during the early deglaciation. Deglacial 234U/238U in the Pacific converged with that in the Atlantic after the abrupt resumption of Atlantic meridional overturning. We suggest that ocean mixing and early deglacial release of excess 234U from enhanced subglacial melting of the Northern Hemisphere ice sheets have driven the observed 234U/238U evolution.

Inter-calibration of a proposed new primary reference standard AA-ETH Zn for zinc isotopic analysis

We have prepared a large volume of pure, concentrated and homogenous zinc standard solution. This new standard solution is intended to be used as a primary reference standard for the zinc isotope community, and to serve as a replacement for the nearly exhausted current reference standard, the so-called JMC-Lyon Zn. The isotopic composition of this new zinc standard (AA-ETH Zn) has been determined through an inter-laboratory calibration exercise, calibrated against the existing JMC-Lyon standard, as well as the certified Zn reference standard IRMM-3702. The data show that the new standard is isotopically indistinguishable from the IRMM-3702 zinc standard, with a weighted δ66/64Zn value of 0.28 ± 0.02‰ relative to JMC-Lyon. We suggest that this new standard be assigned a δ66/64Zn value of +0.28‰ for reporting of future Zn isotope data, with the rationale that all existing published Zn isotope data are presented relative to the JMC-Lyon standard. Therefore our proposed presentation allows for a direct comparison with all previously published data, and that are directly traceable to a certified reference standard, IRMM-3702 Zn. This standard will be made freely available to all interested labs through contact with the corresponding author.