Changes in deep ocean ventilation are commonly invoked as the primary cause of lower glacial atmospheric CO2. The water mass structure of the glacial deep Atlantic Ocean and the mechanism by which it may have sequestered carbon remain elusive. Here we present neodymium isotope measurements from cores throughout the Atlantic that reveal glacial–interglacial changes in water mass distributions. These results demonstrate the sustained production of North Atlantic Deep Water under glacial conditions, indicating that southern-sourced waters were not as spatially extensive during the Last Glacial Maximum as previously believed. We demonstrate that the depleted glacial δ13C values in the deep Atlantic Ocean cannot be explained solely by water mass source changes. A greater amount of respired carbon, therefore, must have been stored in the abyssal Atlantic during the Last Glacial Maximum. We infer that this was achieved by a sluggish deep overturning cell, comprised of well-mixed northern- and southern-sourced waters.
Changes in Atlantic Meridional Overturning Circulation are important in controlling glacial–interglacial climatic shifts due to their role in regulating heat transport in the surface ocean and carbon storage in the deep ocean1,2. Nutrient-based proxy reconstructions suggest that overturning circulation in the Atlantic during the Last Glacial Maximum (LGM) was different to that of the modern ocean3,4,5. These nutrient proxy reconstructions are often interpreted as indicating that during the LGM North Atlantic Deep Water (NADW) shoaled to form Glacial North Atlantic Intermediate Water (GNAIW) and was completely replaced by southern-sourced water in the deep Atlantic (>2.5 km)6,7. However, elucidation of the water mass distribution in such reconstructions is complicated by the fact that the nutrient content of deep waters may vary independently of their source and dynamics8; meanwhile, modelling studies of glacial Atlantic overturning have produced conflicting results9.
In the modern ocean Antarctic Bottom Water (AABW), which is formed in the high latitude Southern Ocean, represents a major inefficiency in the biological pump—the name given to the biologically mediated processes which sequester carbon in the deep ocean. In this region, deep waters are upwelled to the surface, allowing dissolved carbon to be outgassed to the atmosphere, but these waters sink again before their nutrient load can be fully consumed by marine organisms, thus they are said to have a high-preformed nutrient concentration10. The formation of NADW and AABW, and their resultant proportions in the deep ocean thus controls the preformed nutrient concentration of the deep ocean, which, in part, controls atmospheric pCO2 (ref. 11). Ice core records show that atmospheric CO2 concentrations rose by ∼90 p.p.m. between the LGM and the Holocene12. However, considered in isolation, the replacement of high-preformed nutrient AABW with low-preformed nutrient NADW, which has been suggested to have occurred across the last deglaciation, would have increased the efficiency of the biological pump and thereby decreased atmospheric CO2 (refs 11, 13). If our current understanding of glacial–interglacial circulation changes is correct then other parts of the carbon cycle must have counteracted the effects of switching from the GNAIW to NADW mode of deep water formation across the deglaciation. Alternatively, nutrient proxy reconstructions of the Atlantic may be recording carbon cycle changes rather than differences in water mass sourcing.
Neodymium isotopes are a water mass tracer independent of biological processes, allowing deconvolution of changes in water mass sourcing and nutrient regeneration14. Modern NADW has a characteristic ɛNd value (normalized 143Nd/144Nd ratio in parts per ten thousand) of −13.5 (ref. 15) while seawater in the deep Southern Ocean shows ɛNd values around −8.5 (ref. 16), because it has a greater proportion of Pacific Deep Water (PDW) which has an ɛNd of −3.5 (ref. 17). Away from continental margins water masses throughout the deep ocean reflect the quasi-conservative mixing of these deep water masses14. Planktic foraminifera from sea-floor sediment cores have been shown to successfully preserve bottom water ɛNd, thereby offering an archive of past seawater ɛNd (ref. 18).
Here we present Holocene and LGM seawater ɛNd reconstructions, based on foraminiferal ɛNd measurements from 24 cores (Supplementary Table 1, Supplementary Fig. 1) spanning from 46° S to 40° N in the Atlantic Ocean. These reconstructions are used to decipher the nature of changes in Atlantic water mass distributions between glacial and interglacial conditions. Although the LGM reconstruction shows more radiogenic neodymium isotope values than the Holocene profile, the observation of less radiogenic values in the deep North Atlantic than the deep South Atlantic indicates that NADW was produced under glacial conditions. When compared with benthic foraminiferal carbon isotope values, the neodymium isotope measurements reveal that more respired organic carbon was stored in the deep Atlantic Ocean during the LGM than in the Holocene.
Core top foraminiferal ɛNd versus seawater ɛNd
Figure 1 cross plots the Holocene foraminiferal ɛNd values (Supplementary Tables 2 and 3) against the nearest available published seawater ɛNd measurements. Data points were only included in the cross plot if the seawater measurements were within both 10° of latitude and longitude and within 500 m depth of the core site. Most of the data points on the cross plot are within error of the 1:1 line, indicating that foraminifera are faithfully preserving seawater ɛNd. Despite the distance criteria outlined above being applied, the three data points which are outside of error of the 1:1 line are likely due to the seawater data not being of sufficiently close proximity to represent the water mass bathing the core sites. This effect is likely to be particularly prominent in site locations that are near water mass boundaries.
Holocene Atlantic ɛNd reconstruction
We gridded our Holocene foraminiferal ɛNd measurements (Supplementary Table 2) with suitable published data (Fig. 2c). The published data includes results from measurements made on foraminifera, fish debris, high resolution crusts and leachates (Supplementary Tables 3 and 4). As some measurements made on leachates have been shown to be susceptible to contamination by the detrital fraction19,20, results from sites where the core top leachate ɛNd values deviated significantly from nearby seawater values were excluded from the reconstruction. The data points included from the crusts BM1969.05 and TR079 D-14 (Supplementary Table 4) were dated outside of the definition of the LGM used for selecting sediment core data (23–18 ka); however, the records from these crusts were used to argue for the stability of seawater ɛNd across glacial–interglacial cycles in their respective locations21. The slightly older glacial data points from these crusts were therefore deemed appropriate for inclusion in the LGM time slice. DIVA gridding was performed using Ocean Data View22 with the ‘signal-to-noise ratio’ variable set to a value of 25. This variable determines how much a single data point is able to influence the overall plot and this level was chosen to reduce the influence of single data points, as was done by Curry and Oppo4.
The Holocene reconstruction shows the most unradiogenic ɛNd values, around −13, below 1,500 m at the northernmost extent of the plot (Fig. 2c). These values become more radiogenic to the south, with the greatest propagation of this unradiogenic signal centred at 2,000–4,000 m water depth. This is surrounded by areas with more radiogenic ɛNd values, from −8 to −10, at all depths south of 25° S; below 4,000 m from 25° S to the equator; and above 1,500 m at all latitudes. Although the data set is not as extensive as that used in δ13C reconstructions4, this reconstruction replicates the salient features of the seawater ɛNd (Fig. 2a). The only significant mismatches are above 1,000 m at all latitudes and below 4,000 m north of 40° N; in these regions the gridding procedure extrapolates from the nearest data point to the edge of the profile due to a lack of data based constraints. These areas should therefore be interpreted with caution and for this reason the depth range of 0–1,000 m is excluded from later reconstructions.
Last Glacial Maximum Atlantic ɛNd reconstruction
The good correlation between seawater ɛNd and the salinity profile of the modern Atlantic23 demonstrates that the modern seawater ɛNd profile is the result of mixing between northern- and southern-sourced water masses. Collectively, these observations provide confidence that this selection of cores can be used to constrain past Atlantic water mass distributions below 1,000 m. The LGM ɛNd reconstruction (Fig. 3b) shows the most unradiogenic values around −12.5 between 1,500 and 2,000 m extending from the North Atlantic to ∼10° N which then transition to values around −8 at 40° S. In contrast, the deep North Atlantic is occupied by a homogeneous water mass with an ɛNd around −10.5; ɛNd values become more radiogenic to the south, reaching −5.5 at 45° S. The largest differences between the LGM and modern Atlantic profiles occur below 2,500 m (Fig. 3); the deep North Atlantic shifts from ɛNd values around −10.5 in the glacial to −13.5 in the modern ocean, whilst the deep South Atlantic shifts from −5.5 to −8.5. This coherent spatial pattern of changes in ɛNd values in the Atlantic between the LGM and the Holocene (Fig. 3b) is consistent with a change in water mass advection and indicates there was a greater influence of southern-sourced waters in the deep Atlantic under glacial conditions.
The change observed in the deep South Atlantic between the LGM and Holocene (Fig. 3) is consistent with a lower flux of NADW into the Southern Ocean under cooler, glacial conditions24,25. This lower flux of NADW resulted in the deep Southern Ocean being filled with a greater proportion of water of Pacific and Indian Ocean origin that was more radiogenic in composition than Atlantic-sourced deep water26,27,28. The deep South Atlantic, however, remained less radiogenic than the deep Pacific26,28, requiring a source of unradiogenic neodymium to the deep South Atlantic under glacial conditions. Furthermore, the deep North Atlantic was less radiogenic than the deep South Atlantic during the LGM (Fig. 3b); this implies that northern-sourced water with its unradiogenic ɛNd must have been exported to abyssal depths under glacial climate conditions. The mixing of GNAIW with denser southern-sourced waters is deemed an unlikely explanation given the large amount of energy required to mix these intermediate waters down to abyssal depths in the North Atlantic. Rather, these observations suggest that two glacial North Atlantic-sourced water masses existed during the LGM: GNAIW at depths above 2,500 m and denser Glacial NADW (GNADW)29 below 2,500 m.
The inference of a lower flux of GNADW under glacial conditions24 than NADW in the Holocene resulting in a more radiogenic composition of Glacial AABW (GAABW) than AABW would cause the deep Atlantic to exhibit more radiogenic ɛNd values without a change in the water mass mixing proportions in the deep Atlantic. By taking this end-member change of deep southern-sourced water ɛNd into account, however, our results can be used to calculate the proportion of the Atlantic ventilated by NADW (%NADW) both in the Holocene and during the LGM (Supplementary Table 5), and thus elucidate changes in water mass mixing proportions from the effect of the change in the AABW end-member composition. In each case three end-members were required; namely NADW; AABW and Antarctic Intermediate Water, or their glacial counterparts (Supplementary Fig. 2). A binary mixing calculation was performed between a northern- and a southern-sourced water mass at each core site using equation (1). The choice of southern-sourced water varied with depth and latitude according to the observed boundary between Antarctic Intermediate Water and Lower Circumpolar Deep Water as defined by a salinity of 34.7 psu (ref. 30) and the gradient in neodymium concentration (but not ɛNd) between them in the Atlantic sector of the modern Southern Ocean16.
The modern seawater ɛNd and [Nd] end-member values were taken from published seawater data (Supplementary Fig. 2). For the glacial ocean, the ɛNd and [Nd] of NADW and PDW were kept constant; support for the stability of the ɛNd of both comes from crust data31 whilst there is, at present, no proxy for past neodymium concentration available. The more radiogenic ɛNd of GAABW was taken from a South Atlantic record of benthic foraminifera32 and the concentration calculated by conservative mixing of NADW and PDW (ref. 16). Unlike records from the deep South Atlantic26,32, the new intermediate depth glacial foraminiferal ɛNd data from the South Atlantic measured in this work exhibit no changes between the LGM and the Holocene (GeoB2107-3 and GeoB2104-3; Supplementary Table 2), so the neodymium composition of Glacial Antarctic Intermediate Water was assumed to be the same as in the modern ocean. This observation clearly demonstrates that the intermediate and deep South Atlantic were isotopically distinct in terms of neodymium during the LGM, reinforcing the need for two distinct southern-sourced end-member water masses in the mixing calculations.
Figure 4 shows the %NADW values calculated for the Holocene and LGM Atlantic gridded into meridional sections using the same technique employed for the ɛNd data profiles plotted in Fig. 2. In the LGM ɛNd profile (Fig. 3b), the most radiogenic values, around −5.5, are observed at 4,000 m depth in the South Atlantic, whereas less radiogenic values, around −6.5, are seen at ∼5,000 m at the same latitude. The more radiogenic values come from the Mid-Atlantic Ridge; the less radiogenic from the Cape Basin, which lies to the east of the Mid-Atlantic Ridge. The ɛNd difference between these sites likely reflects a longitudinal mixing gradient between radiogenic, Pacific-derived, circumpolar waters28 and less radiogenic North Atlantic derived waters25. A similar phenomenon is seen in modern seawater data from the South Atlantic although the offset is less pronounced16. The results from the deep Cape Basin26 were, therefore, excluded from the mixing proportion plots in Fig. 4 as the longitudinal gradient in ɛNd observed in the deep South Atlantic obscures the latitudinal mixing gradient which is the primary interest here.
The gridded profile of the Holocene %NADW results (Fig. 4a) shows the Atlantic north of 20° N and below 1,500 m depth is mostly (>90%) NADW. %NADW decreases at all depths to the south, with the 50% mixing line occurring near 10° S at 5,000 m, but not until 30° S from 2,000 to 4,000 m. The LGM %NADW contours, including the 50% contour, (Fig. 4b) are similar to the Holocene profile above 2,500 m (Fig. 4a). The greatest difference between the two plots occurs below 2,500 m in the North Atlantic, which has significantly less NADW in the LGM profile (55–80% NADW) than in the Holocene profile (>90% NADW). From this observation it is clear that there was a greater proportion of southern-sourced waters in the deep Atlantic during the LGM than in the Holocene; however, it is also clear that the deep Atlantic was not occupied solely by southern-sourced waters during the LGM.
Although changes in the proportion of NADW in the deep Atlantic between glacial and interglacial conditions are the simplest explanation for the results in Figs 3 and 4, other alternatives must be considered. The sensitivity of the calculated %NADW for the glacial deep Bermuda Rise ɛNd of −10.4 (OCE326-GGC6; 33.7° N, 57.6° W, 4,540 m)18 to the neodymium composition of end-member water masses is shown in Fig. 5. The ɛNd of AABW, considered to be known with reasonable confidence32, was held constant. The ɛNd of GNADW was varied from a near maximum possible value of −10.5 to a minimum of −16.5, similar to the least radiogenic value of −16 that was used in similar calculations performed for a nearby site33. As the %NADW result is dependent on the relative neodymium concentrations of the northern and southern end-members, the ratio of [Nd]GNADW to [Nd]GAABW was varied from 0.2 to 1. The latter value was used in similar calculations performed for a South Atlantic site32 and is used as an upper limit in this work as ratios >1 would require more neodymium dissolved in the deep Atlantic than the deep Pacific, a situation that is not consistent with the observation that neodymium concentrations increase with water mass age in the modern ocean34.
Using the glacial end-member values assigned in Fig. 4, the deep Bermuda Rise site was calculated to be bathed by 72% NADW during the LGM (black box, Fig. 5). In contrast an ɛNd(GNADW) of −10.5 and concentration ratio of 0.2 yields nearly 100% NADW, whilst an ɛNd(GNADW) of −16.5 and a concentration ratio of 1.0 means just 44% NADW is required to explain the ɛNd observed at the Bermuda Rise during the LGM. Although the resultant uncertainty in the %NADW at the Bermuda Rise of ±28% is significant, all end-member configurations yield %NADW in the glacial deep North Atlantic values >44%. This is a robust finding that directly contradicts the notion that the deep Atlantic was dominated by southern-sourced waters during the LGM. Furthermore, the lower estimate of 44% is deemed unlikely to be realistic as less radiogenic ɛNd(NADW) values appear restricted to interstadials, and have been interpreted as pulses of Labrador Sea Water formation during these warm intervals33 or unradiogenic weathering pulses during ice sheet retreat35. Rather, most evidence suggests that ɛNd(GNADW) values were similar to or slightly more radiogenic than NADW in the modern Atlantic21 yielding higher %NADW values (Fig. 5). The influence of analytical error on the calculated %NADW values is small; using the external error bounds of 0.5 epsilon units18 gives a range of 67–77% NADW at the deep Bermuda Rise during the LGM.
Although these uncertainties do limit the certainty of the exact proportion of the deep Atlantic that was ventilated by northern-sourced waters during the LGM, the need for Glacial NADW appears inescapable. If localized processes, such as boundary exchange, were controlling the glacial ɛNd profile, one would expect to see a heterogeneous profile controlled by regional detrital inputs. Furthermore, modelling studies have shown that boundary exchange processes are not able to explain the magnitude of the observed glacial–interglacial shifts in deep ocean ɛNd and thus changes in water mass advection must be invoked to explain them36. Reconstructions of glacial deep water mass ventilation from radiocarbon37, and carbonate ion concentration from B/Ca38,39 also show a younger, better ventilated, water mass in the deep North Atlantic than the deep South Atlantic. These proxies, therefore, also provide evidence for a significant proportion of northern-sourced deep waters in the deep North Atlantic during the LGM, supporting the results shown in Fig. 4.
Reconciling the glacial ɛNd values in the Atlantic with nutrient proxy based reconstructions requires a greater amount of respired organic carbon in the deep glacial Atlantic relative to the modern situation4,8. Circulation versus biological sources of carbon can be differentiated by cross plots of ɛNd against benthic foraminiferal δ13C for the Holocene and LGM Atlantic (Fig. 6). Deep water mass mixing end-members were ascribed to each plot as detailed in the Supplementary Information. The South Atlantic foraminiferal values (grey regions Fig. 6) were corrected for the Mackensen Effect, the phenomenon where benthic foraminifera display δ13C values lower than that of the overlying deep water due to a phytodetrital layer of light organic carbon on the sea floor40. The composition of NADW is similar in the Holocene and LGM cross plots with δ13C and ɛNd values ∼1.4‰ and −13.5, respectively, whereas glacial AABW δ13C is more depleted (−0.5‰) and ɛNd more radiogenic (−5.5) than its modern counterpart (0.4‰, −8.5).
The blue curves show the values expected for conservative mixing between these end-members for each time slice; those points falling along this mixing line have seen little input of biological carbon. During the LGM, data points lying close to the mixing line come from cores shallower than 3,000 m. Most of the glacial data points from cores located below 3,000 m sit well below the mixing curve which we interpret as being caused by the addition of respired organic matter with a low δ13C (usually∼−20‰)41. It is important to note that these cores represent locations within both northern- and southern- sourced glacial deep water, so this signal was not advected from either source but was acquired by biological processes along the advection pathway; this highlights the shortcomings of using δ13C in isolation as a proxy for water mass mixing. The lower than expected δ13C values could also in part be due to the use of mixed Cibicidoides species for some of the benthic foraminiferal δ13C measurements. The variable depth habitats of different Cibicidoides species could lead to offsets of the measured foraminiferal calcite δ13C from bottom water δ13C (ref. 42). The inference of organic matter remineralization being the dominant cause of the offset, however, is supported by a recent study that modelled the glacial Atlantic and predicted a biological regenerative imprint in the glacial deep Atlantic δ13C (ref. 8). The same study calculated that, after allowing for this remineralisation of organic matter, the glacial deep North Atlantic was ventilated by 50–80% NADW, which compares well with the ɛNd derived values of 55–80% NADW produced in this work (Fig. 4b).
The accumulation of respired organic carbon in the deep Atlantic during the LGM could be due to higher surface productivity and thus export of organic carbon to the deep ocean under glacial climate conditions. Although glacial productivity reconstructions in the northwestern Atlantic are sparse, nearby regions show elevated export production during the LGM relative to the Holocene43. Higher glacial surface productivity, however, cannot explain the depth dependence of the δ13C offset in the LGM (Fig. 6b), nor can it explain the chemocline seen at ∼2,500 m in nutrient proxy reconstructions3,4. Thus it seems likely that the greater amount of respired organic matter in the deep Atlantic during the LGM must have also been at least partially due to a longer residence time of seawater in the glacial deep Atlantic than in the modern Atlantic. This conclusion is supported by a modelling study of a 231Pa/230Th data compilation which concluded that the glacial Atlantic had rapid overturning in the shallow cell but slower overturning at depth44.
Our findings are summarized in hypothetical overturning schematics for the Atlantic Ocean during glacials and interglacials in Fig. 7. In the glacial scenario (Fig. 7b) there are two distinct northern-sourced water masses, separated by density differences. The glacial northern-sourced intermediate depth water mass was likely formed by convection south of Iceland45 and is inferred to have overturned rapidly44. The deep Atlantic cell is surmised to have overturned more slowly and may have been supplied by NADW formed in the Nordic Seas during seasonal ice-free periods coming over the Greenland-Scotland Ridge46. Brine rejection from sea ice may also have contributed to this process47. A lower flux of GNADW during the LGM than NADW in the Holocene in to the deep North Atlantic would then explain how AABW was able to penetrate much further north during the LGM (Fig. 4b) than in the modern Atlantic Ocean where it has little influence north of the equator (Fig. 4a). In contrast, the deep South Atlantic shows less of a change in water mass mixing proportions between the LGM and the Holocene (Fig. 4) because it is dominated by southern-sourced waters in both climate states (Fig. 7).
Many modelling studies and hypothesized glacial overturning schemes invoke GNAIW being incorporated into deep waters elsewhere in the glacial ocean to ventilate the deep ocean with low-preformed nutrient concentration water10,13,48. Here, we have presented evidence that instead the deep Atlantic was ventilated directly from the North Atlantic resolving the difficulty in reconciling glacial CO2 drawdown with the observed proxy data. Another important prediction of our work is that switching from the glacial to interglacial mode of North Atlantic circulation (Fig. 7) would flush respired organic carbon from the deep Atlantic and would therefore be expected to raise atmospheric CO2 without invoking changes in nutrient utilization in the high latitude Southern Ocean13. Although a full carbon cycle model would be required to quantify this effect, the resumption of strong NADW production at the start of the Bølling-Allerød inferred from ɛNd and 231Pa/230Th records, coincides with a ∼12 p.p.m. increase in atmospheric CO2 (Supplementary Fig. 3)12,18,49. This increase likely reflects the flushing of respired carbon from the deep Atlantic by strong NADW production during the deglaciation50.
ɛNd measurements were made on uncleaned planktic foraminifera from Holocene and LGM samples of cores from throughout the western Atlantic basin or selected regions within the eastern Atlantic (Fig. 2d); all core names and locations are listed in Supplementary Table 1 and plotted in Supplementary Fig. 1. Eastern Atlantic cores were limited to sites south of the Walvis Ridge or sites on bathymetric rises above the sill depth of the Mid-Atlantic Ridge (3,750 m)51. This selection was based on the criteria outlined by Curry and Oppo4, and was intended to avoid the regions of the eastern Atlantic which are ventilated through fracture zones in the Mid-Atlantic Ridge and thus do not display the same latitudinal water mass mixing gradient as the western Atlantic52. Cores north of 45° N were excluded as they have been shown to be susceptible to the influence of volcanic ash and IRD in the North Atlantic19,53.
Age controls for cores used in this work range from planktic or benthic foraminiferal δ18O records to radiocarbon dates (Supplementary Table 1) and came from published age models, with the exception of the Ceara Rise cores. The radiocarbon-based age models developed in this work for the latter cores, ODP 925E, ODP 928B and ODP 929B, are presented in Supplementary Table 6. For all cores, depths which were assigned calendar ages between 23 and 18 ka were included in the LGM reconstruction.
Samples were prepared for analysis following the methods of Roberts et al.18 and references therein. In short, where possible, ∼80 mg of mixed planktic foraminifera were picked from the coarse fraction (>63 μm) for neodymium isotope measurements. After picking, foraminifera tests were broken open between two glass plates, rinsed, sonicated and any clays removed. The samples were then dissolved in 1 mol l−1 reagent grade acetic acid. The REEs were extracted from the dissolved sample using Eichrom TRUspec resin in 100 ml Teflon columns. Neodymium was then separated from the other rare earth elements using Eichrom LNspec resin on volumetrically calibrated Teflon columns.
Neodymium isotopic measurements
Neodymium isotopes were analysed using the Nu Plasma HR or Neptune Plus multi-collector inductively coupled plasma mass spectrometers at the University of Cambridge. 146Nd/144Nd was normalized to 0.7219 and samples were bracketed with a concentration-matched solution of reference standard JNdi-1, the measured composition of which varied between runs but was corrected to the accepted value of 143Nd/144Nd=0.512115 (ref. 54). The ɛNd of each sample is reported with the external error (2σ) of the bracketing standards from the corresponding measurement session, unless the internal error was larger than the external error, in which case the combined internal and external error (2σ) is reported.
Eight complete procedural blanks for the process from foraminiferal dissolution through to column chemistry were run on a TIMS Sector 54 at the University of Cambridge using a 150Nd spike. For the typical sample, of at least 15 ng, the average blank of 66 pg of neodymium is <0.5% of the total neodymium.
Benthic foraminiferal stable isotopes
Benthic foraminifera (mixed Cibicidoides species; between 3 and 7 tests) were picked for stable isotope analysis from the coarse fraction (>125 μm) of samples without published δ13C data. Samples were analysed by the Godwin Laboratory at the University of Cambridge using either a Micromass Multicarb Sample Preparation System attached to a VG SIRA or a Thermo Kiel device attached to a Thermo MAT253 Mass Spectrometer in dual inlet mode. Isotopic ratios are presented relative to standard Vienna PeeDee Belemnite; external precision was ±0.06‰ for δ13C.
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Sample material was provided by the Godwin Laboratory for Paleoclimate Research at the University of Cambridge, the International Ocean Discovery Program the GeoB Core Repository at the MARUM—Center for Marine Environmental Sciences, University of Bremen and Petrobras. We thank Jo Kerr and Aurora Elmore for providing additional samples. We thank Thiago Pereira dos Santos for providing the unpublished age model data for GL1090; we thank Jo Clegg and Vicky Rennie for technical support and Natalie Roberts for helpful discussions. Radiocarbon analyses were supported by NERC radiocarbon grant 1752.1013 and Nd isotope analyses by NERC grants NERC NE/K005235/1 and NERC NE/F006047/1 to A.M.P. J.N.W.H. was supported by a Rutherford Memorial Scholarship. S.M. was supported through the DFG Research Center/Cluster of Excellence ‘The Ocean in the Earth System’. C.M.C. acknowledges financial support from FAPESP (grant 2012/17517-3).
The authors declare no competing financial interests.
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Howe, J., Piotrowski, A., Noble, T. et al. North Atlantic Deep Water Production during the Last Glacial Maximum. Nat Commun 7, 11765 (2016). https://doi.org/10.1038/ncomms11765
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