Abstract

The origin and carbon content of the deep water mass that fills the North Atlantic Basin, either Antarctic Bottom Water (AABW) or North Atlantic Deep Water (NADW) is suggested to influence the partitioning of CO2 between the ocean and atmosphere on glacial–interglacial timescales. Fluctuations in the strength of Atlantic meridional overturning circulation (AMOC) have also been shown to play a key role in global and regional climate change on timescales from annual to millennial. The North Atlantic is an important and well-studied ocean basin but many proxy records tracing ocean circulation in this region over the last glacial cycle are challenging to interpret. Here we present new B/Ca-[CO32−] and boron isotope-pH data from sites spanning the North Atlantic Ocean from 2200 to 3900 m and covering the last 130 kyr from both sides of the Mid-Atlantic Ridge. These data allow us to explore the potential of the boron-based proxies as tracers of ocean water masses to ultimately identify the changing nature of Atlantic circulation over the last 130 kyr. This possibility arises because the B/Ca and boron isotope proxies are directly and quantitatively linked to the ocean carbonate system acting as semi-conservative tracers in the modern ocean. Yet the utility of this approach has yet to be demonstrated on glacial–interglacial timescales when various processes may alter the state of the deep ocean carbonate system. We demonstrate that the deep (∼3400 m) North Atlantic Ocean exhibits considerable variability in terms of its carbonate chemistry through the entirety of the last glacial cycle. Our new data confirm that the last interglacial marine isotope stage (MIS) 5e has a similar deep-water geometry to the Holocene, in terms of the carbonate system. In combination with benthic foraminiferal δ13C and a consideration of the [CO32−] of contemporaneous southern sourced water, we infer that AABW influences the eastern abyssal North Atlantic throughout the whole of the last glacial (MIS2 through 4) whereas, only in the coldest stages (MIS2 and MIS4) of the last glacial cycle was AABW an important contributor to our deep sites in both North Atlantic basins. Taken together, our carbonate system depth profiles reveal a pattern of changing stratification within the North Atlantic that bears strong similarities to the atmospheric CO2 record, evidencing the important role played by ocean water mass geometry and the deep ocean carbonate system in driving changes in atmospheric CO2 on these timescales.

Highlights

  • Analytical techniquesSediment samples from core material were washed with deionised water and sieved to >63 m, to separate fine and coarse fractions

  • B/Ca data were gathered in isolation for around 40-70 sample intervals per core (~1 per 2-4 kyrs) and around 30 tests of C. wuellerstorfi were separated from ~20 (1 per 7 kyrs) sediment samples for separate δ11B measurements

  • Samples were measured for boron isotope composition on Thermo Scientific Neptune MC-ICPMS at the University of Southampton, following previous protocols (Foster, 2008)

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Summary

Analytical techniques

Sediment samples from core material were washed with deionised water and sieved to >63 m, to separate fine and coarse fractions. As all work is carried out on shallowly buried well preserved tests, the level of physical cleaning (Barker et al, 2003) could be reduced to minimise sample loss, though strict criteria are used to rule out clay contaminated results (samples with Al/Ca >100μmol/mol removed). For those samples analysed for δ11B only, an aliquot of ~10% was removed from the cleaned and dissolved sample for elemental analysis for this purpose. Clay contamination can be a problem for boron isotope analysis due to the relatively high concentration of boron in clays (B3+ can substitute for Al3+) and the low δ11B of clay derived boron (Deyhle and Kopf, 2004; Oi et al, 1989)

Determination of boron isotopic composition
Element ratios
Carbonate system reconstructions and calculations
Full Text
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