Abstract
Efforts to improve sea level forecasting on a warming planet have focused on determining the temperature, sea level and extent of polar ice sheets during Earth’s past interglacial warm periods1,2,3. About 400,000 years ago, during the interglacial period known as Marine Isotopic Stage 11 (MIS11), the global temperature was 1 to 2 degrees Celsius greater2 and sea level was 6 to 13 metres higher1,3. Sea level estimates in excess of about 10 metres, however, have been discounted because these require a contribution from the East Antarctic Ice Sheet3, which has been argued to have remained stable for millions of years before and includes MIS114,5. Here we show how the evolution of 234U enrichment within the subglacial waters of East Antarctica recorded the ice sheet’s response to MIS11 warming. Within the Wilkes Basin, subglacial chemical precipitates of opal and calcite record accumulation of 234U (the product of rock–water contact within an isolated subglacial reservoir) up to 20 times higher than that found in marine waters. The timescales of 234U enrichment place the inception of this reservoir at MIS11. Informed by the 234U cycling observed in the Laurentide Ice Sheet, where 234U accumulated during periods of ice stability6 and was flushed to global oceans in response to deglaciation7, we interpret our East Antarctic dataset to represent ice loss within the Wilkes Basin at MIS11. The 234U accumulation within the Wilkes Basin is also observed in the McMurdo Dry Valleys brines8,9,10, indicating11 that the brine originated beneath the adjacent East Antarctic Ice Sheet. The marine origin of brine salts10 and bacteria12 implies that MIS11 ice loss was coupled with marine flooding. Collectively, these data indicate that during one of the warmest Pleistocene interglacials, the ice sheet margin at the Wilkes Basin retreated to near the precipitate location, about 700 kilometres inland from the current position of the ice margin, which—assuming current ice volumes—would have contributed about 3 to 4 metres13 to global sea levels.
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Main
Large uncertainties in reconstructions of sea level highstands during Earth’s past warm interglacial periods, as well as in the predictions of future sea level rise, result in part from the poorly constrained climate sensitivity of the East Antarctic Ice Sheet (EAIS). The EAIS is the world’s largest freshwater reservoir and ice loss in response to a warming climate is expected to be focused on the low-elevation basins most susceptible to grounding line retreat, including the Wilkes, Pensacola and Aurora basins14, which could collectively contribute 8–10 m in sea level rise15 (Fig. 1). Yet an idea that has prevailed for decades argues that the EAIS has remained stable on million-year timescales4,5. The apparent stability of East Antarctica is inferred primarily from the preservation of ancient glacial features, slow erosion and a lack of evidence for major melting within the Transantarctic Mountains4,5, the polar desert range that borders the EAIS (Fig. 1). Although this result was initially supported by ice-sheet models that required unrealistic warming (>10 °C) to yield ice loss16, recent models that incorporate ice–ocean interactions do predict an East Antarctic response to modest warming within low-elevation basins, including the Wilkes Basin, while preserving ice in the Transantarctic Mountains13,14. The susceptibility of the marine basins to deglaciation has gained support from observations gathered from Pleistocene sediment cores collected offshore of the Wilkes Basin17. These data reveal oscillations in the provenance of detrital sediment that have been interpreted to reflect a shift from coastal to on-continent erosion driven by Wilkes Basin ice loss during interglacial periods MIS5, MIS9 and MIS11 that was greater than the ice loss observed in the Holocene. Despite these theoretical advances and observations, which have shifted scientific views towards a more dynamic EAIS, neither the computational models nor offshore sedimentary records are capable of determining both the timing and magnitude of EAIS deglaciation during Pleistocene interglacials. These past interglacial warm periods are characterized by global warming of 1–2 °C above preindustrial temperatures, a substantial warming increase that is analogous to projected near-future climate change1. Thus, any additional means of recognizing the timing and magnitude of past ice-loss events in East Antarctica in response to warming may clarify the height of sea level highstands in both the past and future.
Such additional methods for documenting ice sheet collapse have recently been developed by Chen and others7 who showed that the collapse of the Laurentide ice sheet 15–20 thousand years ago (ka) was associated with a transient 3‰ increase in the δ234U (where δ234U = [(234U/238U)AR − 1] × 1,000) composition of Atlantic waters relative to modern seawater. Aqueous enrichment in 234U above secular equilibrium (δ234U = 0‰) reflects rock–water interaction18 and in glacial systems may be attributed to the recoil injection of 234U into basal ice and subglacial waters incurred during the α-decay of parent 238U housed within debris-laden basal ice and subglacial sediments (Fig. 2, bottom inset). From the change in ocean water compositions, Chen and others7 inferred that a reservoir strongly enriched in 234U within the Laurentide ice sheet was flushed rapidly into the ocean during early phases of the last glacial termination. They pointed to the brines of the McMurdo Dry Valleys, Antarctica, which currently exhibit δ234U compositions greater than 3,000‰ (refs. 8,10), as a possible analogue to the Laurentide 234U-enriched reservoir.
Results
Here we report results from a new Antarctic archive of δ234U compositions: chemical precipitates formed in subglacial aquatic environments beneath the EAIS. These aqueous chemical precipitates form as a byproduct of subglacial freezing, a process that consumes subglacial waters, concentrating solutes to the point of calcite19,20 or amorphous silica/opal21,22 precipitation. The oxygen compositions of Antarctic calcite precipitates are among the most 18O-depleted compositions on Earth20,23,24, which confirms their precipitation from Antarctic subglacial waters23. Precipitates sampled from either deglaciated bedrock surfaces23,24 or from exposed sections of basal ice or moraines20,25 place the location of precipitate formation beneath the ice. Because they can be dated by 234U–230Th methods (see Methods), these precipitates record the δ234U of subglacial waters at the time of sample precipitation (δ234Ui) and collectively reveal that 234U enrichment is not limited to the waters of the McMurdo Dry Valleys alone, but rather, is observed to be both geographically and temporally ubiquitous in the aquatic environments of East Antarctica (Fig. 1).
Figure 1 shows the distribution of both new (Extended Data Table 1) and existing24,25,26 U-series data for five EAIS precipitate locations, four of which border the EAIS along the Transantarctic Mountains within the Pensacola and Wilkes basins; the fifth lies within the Aurora basin. Precipitates from each of these locations exhibit δ234Ui compositions well in excess of secular equilibrium and marine compositions (δ234U = 145‰ (ref. 27), Fig. 1). These observations imply that subglacial waters are the source and cause of change in marine δ234U (ref. 7) 15–20 ka and inform us that basal waters from the Laurentide ice sheet were flushed in advance of large-scale deglaciation. A comparison between the 234U–230Th date and the δ234Ui for EAIS precipitates yields an apparent shared history for this continent-scale compilation that is characterized by 234U accumulation, with δ234Ui increasing by >2,000‰ over the past 300 ka or so (Fig. 3). Part of this long-term archive of 234U accumulation is recorded in a single geographic location by a subglacial precipitate sample from Elephant Moraine (PRR50489). This centimetre-thick sample of layered opal and calcite has been dated at multiple horizons, revealing 234U–230Th dates from 265 ka to 150 ka and record changes of δ234Ui within the subglacial waters of the Wilkes subglacial basin of >700‰ (Fig. 3). An additional sample from Elephant Moraine (PRR39222) also exhibits variations in δ234U with stratigraphic position. Though low U/Th for PRR39222 inhibits a reliable age determination, the measured δ234U values, uncorrected for 234U decay, are approximately 40–140‰ and correlate with stratigraphic position (the top corresponds to higher δ234U, Extended Data Table 1). With the formation time unknown, we can instead model the δ234Ui values for formation 0–450 ka for both the top and bottom of the sample (Fig. 3, purple curves). If we assume sample precipitation rates (0.5–5 mm kyr−1) similar to Antarctic calcite dated by U–Th methods (for example, PRR50489) we can define a formation duration for PRR39222 (45 mm) of about 10–90 kyr. Assuming these durations, along with the requirement that the bottom and top of the sample intersect the purple curves shown in Fig. 3, permits the definition of possible δ234Ui ingrowth (that is, the production and accumulation of radiogenic daughter products) histories (black arrows, Fig. 3). We find that possible ingrowth histories are congruent with the shared δ234Ui ingrowth history for the region if this sample formed about 400 ka (Extended Data Fig. 3) but incongruent at earlier formation times (Extended Data Fig. 3). Although uncertainty on the age of PRR39222 remains, the occurrence of low δ234U (<500‰) in subglacial fluids is apparently rare (Fig. 3), having been identified in this region only in samples older than about 300 kyr (with the exception of a single outlier in the Taylor Valley dataset). This suggests that PRR39222 records the ingrowth of 234U within Wilkes Basin waters at about 300–400 ka.
As introduced above, 234U enrichment has been recorded in waters of the McMurdo Dry Valleys. The McMurdo Dry Valleys are the largest ice-free area of Antarctica, where land-terminating glaciers permit subglacial brines to emanate onto the surface or into proglacial lakes11. The source of McMurdo Dry Valleys fluids has been extensively studied: the geochemistry10, isotopic composition28 and bacterial ecosystems12 all point to origination from a marine flooding event that occurred before isolation of fluids from the atmosphere on timescales greater than 200 kyr29,30 (see Methods for further discussion). Citing observations of ancient preserved features and slow erosion within the Transantarctic Mountains4,5, the timing of the marine incursion associated with McMurdo Dry Valleys brines has often been relegated to occurring millions of years ago in the warmer Miocene climate10,12. Modern McMurdo Dry Valleys brines and surface lakes found in both the Taylor and Wright valleys, however, are observed to share characteristics with fluids beneath the EAIS: they are currently strongly enriched in 234U (Fig. 1, δ234U > 3,000‰)8,10. Carbonates that formed within past proglacial lakes of Taylor Valley also record elevated δ234U values9, suggesting that these palaeolakes, like modern Lake Bonney11, were also fed by subglacial waters. Similar to the subglacial precipitates in the EAIS, we note that the existing data for these McMurdo Dry Valleys lake carbonates document an increase in δ234Ui over the past 300 kyr or so (Fig. 3a). This coevolution of δ234U in McMurdo Dry Valleys and EAIS fluids supports the view that McMurdo Dry Valleys brines formed much more recently than the Miocene and have been sourced from subglacial EAIS fluids within the Wilkes Basin that have been cryoconcentrated in transit by subglacial freezing11.
The accumulation to high values (>3,000‰) and the evolution of δ234Ui with time as recorded by EAIS precipitates, McMurdo Dry Valleys lake carbonates and modern fluids both match the model predictions of 234U ingrowth by direct injection into fluids during the decay of 238U housed within subglacial sediments (Fig. 2 and Supplementary Information). Collectively, these data point to a subglacial water reservoir starting with low δ234U compositions that have increased by 234U recoil ejection from sediments but that has not yet reached a steady-state δ234U composition (δ234USS), which is attained after >1 million years of rock–water contact (Fig. 2). To place an estimate on the duration of rock–water contact, we employ a model that simulates 234U ingrowth histories from α recoils and explores two key variables: the onset time and the δ234USS (see Supplementary Information). A number of physical variables influence the rate of 234U ingrowth and δ234USS, including sediment grain size, uranium content and porosity (Fig. 2). For the purposes of estimating the timing of reservoir inception, we need not uniquely determine any of these reservoir traits which, given their occurrence beneath the EAIS, are poorly known. Rather, we can explore extreme ranges of all variables via their net effect on δ234USS and identify, using a maximum likelihood test, the model ingrowth histories that best match the measured data. However, it is expected that the physical traits controlling 234U accumulation differ from one subglacial reservoir to the next (Fig. 2). For example, the approximately 2,000‰ range in δ234U observed between modern waters and young (<25 kyr) precipitates from across East Antarctica probably reflects differences in the sediment characteristics between these geographically and geologically distinct regions (Fig. 3). This heterogeneity does not apply to sample PRR50489, a centimetre-thick sample that provides a >100-kyr record of 234U accumulation beneath the ice in a single location. Using a maximum-likelihood test, we compare the measured results for PRR50489 with model simulations of 234U ingrowth for a range of reservoir isolation times (100–800 kyr), initial δ234U (that is, δ234Ui) for the subglacial reservoir (0–1,500‰) and δ234USS (2,000–9,000‰). The uncertainty in the timing of reservoir isolation is dominated by the possible range of δ234Ui compositions for the reservoir. Assuming values as low as those observed in sample PRR39222 or marine compositions (145‰), best-fit paths correspond to reservoir inception times of \({435}_{-25}^{+20}\,{\rm{k}}{\rm{a}}\) (95% confidence interval, χν2 = 3.9) (Fig. 3b, c). If the reservoir were initially enriched in 234U, perhaps up to 500‰ as in the oldest carbonates found in Taylor Valley, the best-fit path is shifted with an inception time of \({390}_{-15}^{+25}\,{\rm{k}}{\rm{a}}\) (95% confidence interval, χν2 = 3.9) (Fig. 3c). Thus, even assuming a range of δ234Ui compositions that lie between sample PRR39222 and the oldest Taylor Valley carbonates, we identify a reservoir inception time coincident with MIS11. In contrast, for reservoir isolation to have begun during the next interglacial (MIS9) would require a δ234Ui in subglacial waters of >1,000‰ (Fig. 3c), consistent with the lowest values observed in Elephant Moraine sample PRR50489. The formation of subglacial samples during subsequent interglacials (MIS5, MIS7), along with documented 234U accumulation during these times, is inconsistent with MIS5 or MIS7 ice loss and instead point to an earlier reservoir isolation that permits 234U to accumulate to the values observed.
Discussion and conclusions
Measured data from both EAIS precipitates and carbonates from the McMurdo Dry Valleys unequivocally record 234U accumulation within fluids that initiated at δ234U values lower than present (Fig. 3). Our documented accumulation does not reflect a 234U system in steady state (black dashed line, Fig. 3) and are thus inconsistent with fluids that have experienced isolation and contact with rocks on million-year durations. Collectively, these observations are inconsistent with models for extreme EAIS stability on million-year timescales. Rather, these data require that the subglacial reservoir within the low-elevation Wilkes Basin began at a lower δ234U and remained at least partially isolated with respect to uranium for only about 400 kyr. Without such isolation 234U would not have accumulated, requiring that over the past 400 kyr or so, the evacuation and replacement of 234U-enriched fluids from the ice sheet base was exceeded by 234U enrichment. The accumulation of 234U in this isolated to partially isolated reservoir implies ice stability over the past 400 kyr. The lower δ234U values inferred at MIS10 to MIS11, however, imply that the replacement of 234U-enriched fluids, perhaps by flushing of basal waters or ice cap retreat, did outpace 234U ingrowth at this time. This interpretation of the 234U accumulation record in East Antarctica draws on the observed 234U cycling in the Laurentide ice sheet, where 234U-enriched subglacial waters were documented at the peak of Laurentide ice extent/volume (25 ka)6, but the reservoir was released to global oceans in response to deglaciation7. Although any record of 234U accumulation beneath the EAIS before MIS11 is not reflected in the data presented here, we may infer from the documentation of 234U enrichment beneath the Laurentide6,7, Cordilleran22, Iceland31, Greenland32 and Antarctic ice masses that 234U accumulation occurs in response to protracted rock–water contact in an isolated or partially isolated reservoir. On the basis of the documented response in Atlantic coral δ234Ui to Laurentide deglaciation7, we suggest that any pool of pre-MIS11 234U-rich waters stored beneath the EAIS as well as Greenland and West Antarctica (see below) was released to the oceans, which may explain, in conjunction with diagenetic effects, why the δ234Ui compositions of MIS11 corals record a change in marine δ234Ui compositions33 a factor of ten greater than the change recorded7 in response to the most recent deglaciation .
There are few possible ice-sheet responses to MIS11 warming that may have led to the observed cycling in δ234U. Increased warming could have led to enhanced glacial ablation on the EAIS, complete with surface melting, moulin formation and flushing basal waters that reset the 234U accumulation at the base of the ice. The basal flushing volumes required to lower the δ234U within subglacial waters are 3–4 orders of magnitude higher than estimates of present-day subglacial water volumes (Extended Data Fig. 5, Methods and Supplementary Information). The question arises of whether MIS11 warming was sufficient to induce such surface melting and meltwater penetration to the bed, within the Wilkes Basin. Ice-sheet models14 and our current climate do not support this response and instead show that EAIS retreat within the marine basins would have to be driven by ocean–ice interactions, which would occur before sufficient warming to permit surface melting and basal flushing at such high volumes. In short, polar conditions like today’s would have persisted on the ice surface even as the ice mass retreated within the low-elevation marine basins in response to warming oceans.
Thus, an alternative explanation to basal flushing for the observed cycling in δ234U is that the Wilkes Basin grounding line moved closer to the precipitate sampling locations during MIS11 as a result of ice interaction with warming oceans (Fig. 1). Under such a mechanism for removal of 234U-enriched waters, the geographic position of subglacial precipitates could be used to infer whether ice in a specific location remained stable or was lost at a particular point in time. For example, the Elephant Moraine samples derive from a glacial catchment that extends into the Wilkes Basin about 700 km inboard of the current grounding line (Fig. 1). The loss of 234U at this location implies substantial retreat within the Wilkes Basin at MIS11. Such a collapse is plausible: the inland-sloping topography of Wilkes Basin makes grounding-line retreat in this region susceptible to a positive feedback that could produce more than 800 km of grounding-line migration13. And while basal flushing and grounding-line retreat could work hand-in-hand to some extent, the width of an ablation zone within a retreating ice sheet at high latitudes would be sufficiently narrow (<30 km)34,35 to render the relative contribution of flushing to resetting 234U accumulation relatively minor when compared to the hundreds of kilometres of grounding-line migration required to affect the samples studied here. In other words, these samples are so far inland, and the conditions are still so cold, that grounding-line retreat must be the dominant mechanism for 234U resetting.
If ice retreated from Wilkes Basin, which lies below sea level, it would fill with seawater, replacing or mixing with high-δ234U-composition waters. Following MIS11, the subsequent re-advance of ice over marine sediments with connate seawater would impart marine signatures to subglacial waters, consistent with the geochemical, isotopic and biogeochemical evidence for marine sourcing of McMurdo Dry Valleys fluids10,12. In addition, proposed ice loss in MIS11 within the Wilkes Basin is consistent with glaciological evidence and with maximum meteorite terrestrial ages at the Elephant Moraine of around 400 kyr (see Methods for further discussion). The accumulation of 234U at the Elephant Moraine throughout MIS5, MIS7 and very likely MIS9 (Fig. 1) suggests that any ice loss during these shorter-duration warmer periods, as resolved by offshore sedimentary records17, did not reach this far back into the Wilkes Basin.
Indeed, offshore sedimentary archives record a more pronounced on-continent weathering signal during MIS11 than in subsequent interglacials17. At the warmer and longer MIS11 interglacial the EAIS grounding line must have retreated to the proximity of the Elephant Moraine, about 700 km inland from the current coastline. A minimum contribution of Wilkes Basin collapse to global sea level at MIS11 can be estimated if we assume that: (1) grounding-line retreat was not accompanied by ice-sheet thickening, as invoked for warmer Pliocene conditions36, and (2) ice volumes before MIS11 warming were at least comparable with the current, well known ice volumes13. Both assumptions are probably safe. Models predict36 ice thickening during Pliocene warmth where low sea-ice coverage leads to increased precipitation, conditions that do not apply to the colder Pleistocene. Similarly, ice volumes within the Wilkes Basin before MIS11 warming are likely to be comparable or greater than at present. Preceding MIS11 warming, MIS12 was one of the coldest glacial periods of the Pleistocene2, whereas currently, during one of the warmest Pleistocene interglacials, the basin contains ice volumes that would contribute an estimated 3–4 m (ref. 13) to global sea level rise in response to the reported extent of Wilkes Basin grounding-line retreat.
The record presented here tightly brackets the EAIS response to a warming world: 1–2 °C warming during the long MIS11 interglacial, with the warmest temperatures observed since about 2 million years ago, resulted in hundreds of kilometres of grounding-line retreat, while similar temperatures during the subsequent and shorter MIS5 and MIS9 interglacials did not result in a comparable retreat. Our interpretation of a diminished MIS11 ice sheet in the Wilkes Basin that contributed several metres to global sea level is also consistent with distal geologic data for the sea level during this interglacial. Sea-level reconstructions resulting from MIS11 warming are up to 4 m higher than the subsequent interglacials, suggesting that the Wilkes Basin may account for the difference in sea-level highstands. The MIS11 highstands of 6–13 m3 have been attributed to the near-complete collapse of the Greenland (4.5–6 m; ref. 37) and West Antarctic (3.2–5 m; ref. 38) ice sheets alone3, which can account for a maximum of only 11 m. The 700 km of grounding-line retreat reported here would very probably result in several metres of global sea-level rise, suggesting that MIS11 highstands greater than 11 m and perhaps as high as 13 m may occur in response to 1–2 °C of global warming.
Methods
U-series methods
234U–230Th dates were produced at the University of California Santa Cruz (UCSC) Keck Isotope Laboratory. Sample digestions were carried out using either 7N HNO3 (calcite) or concentrated HF + HNO3 (opal). Samples were spiked with a gravimetrically calibrated mixed 229Th–236U tracer and dried down. U and Th separates were purified using an ion chromatography procedure that used 1 ml of AG1-X8 anion resin. Total procedural blanks for U and Th were <5 pg and minor relative to sample sizes. Uranium isotopic measurements were conducted using the IsotopX X62 Thermal Ionization Mass Spectrometer (TIMS) housed at UCSC and measured uranium as UO2 using a Si-gel emitter. Uranium compositions were corrected for oxide isobaric interferences following ref. 42. Mass-dependent fractionation correction was applied using a linear correction with the correction factor determined from long-term measurement of standards. Uranium dead times for the Daly were calibrated using NBS U-500. Accuracy of the uranium method was evaluated using the uranium standard NBS4321. Extended Data Fig. 4 shows NBS4321 analyses measured over the duration of this study. Thorium isotopic determinations used the UCSC TIMS, by graphite loading and a Daly peak hopping routine. Thorium fractionation and dead time were estimated by running NBS U 500 as a metal. 234U–230Th date accuracy was tested using MIS5e coral dated by Hamelin and others43, an in-house opal standard in secular equilibrium and subglacial carbonate precipitate previously dated by Frisia et al.24 (Extended Data Table 3). U–Th ages are calculated using codes designed at UCSC. Decay constants for all data and models were from Cheng et al.44. All uncertainties are reported at 2σ. Mass spectrometry methods are described in greater detail in Supplementary Information.
Simulating porewater δ234U evolution
The δ234U enrichment in subglacial settings could result from direct injection or preferential leaching of 234U from glacial sediments into subglacial waters. Preferential leaching of 234U relative to 238U has experimentally been shown to increase fluid δ234U to marine-like compositions on laboratory timescales; however, there is a finite pool of leachable 234U in rocks, such that on longer residence times (>104 yr) both natural and experimental waters reveal submarine δ234U (ref. 45). In the EAIS, however, the accumulation to high δ234U values (4,000‰) and the topology of δ234Ui with time both match the model predictions of 234U accumulation by direct injection into fluids incurred during the decay of 238U housed within subglacial sediments. Collectively, these data point to a subglacial water reservoir that initiated with low δ234U compositions and then increased by 234U recoil injection but has yet to reach the δ234USS value that the 234U system would attain after approximately a million years of rock–water contact. The time-dependent evolution of 234U in sediment porewaters may be described by a model presented in Supplementary Information. Using this model, simulated 234U/238U fluid evolutions are evaluated by comparison with the measured data using a maximum-likelihood test (also detailed in Supplementary Information).
Influence of hydrological flushing on δ234U of subglacial waters
Our analyses of subglacial precipitates record a progressive increase in δ234U of subglacial waters, from which these precipitates formed, since MIS11, when the δ234U reservoir has been reset to very low values. We consider here (and within Supplementary Information, where the model is described in full with equations) whether this MIS11 resetting event may have had to do simply with an increase in basal melting, for example, caused by thickening of the ice sheet due to a warming-induced increase in precipitation46, and the associated increase in hydrological flushing rates of the subglacial water reservoir. The results of this model show that only very short flushing timescales, of <10 years, result in low values of the steady-state activity ratio. We expect that comparably low values were reached during the event that reset the δ234U values during MIS11 (Fig. 3). This result applies to other combinations of parameters beyond the ones illustrated in Extended Data Fig. 5. For instance, similar curves can be obtained for a weathering timescale of ten million years as long as the 234U ejection factor is about ten times larger than the values shown in Extended Data Fig. 5, which would require finer-grained subglacial sediments. It is useful at this point to estimate, for reference, what is the flushing rate for the subglacial zone of the modern Antarctic ice sheet. Pattyn41 used a numerical ice-sheet model to calculate that basal melting produces approximately 65 km3 of melt per year. Assuming no large change in subglacial water storage and allowing for some losses to infiltration into deep groundwater systems (for example, see ref. 47) and to basal freezing, this means that the continental-scale hydrological throughflow rate is approximately a few tens of cubic kilometres per year. Dowdeswell and Siegert48 estimated that subglacial Antarctic lakes alone contain about 10,000 km3. Another large water reservoir that is hydrologically connected to the basal meltwater system is the porewater in subglacial tills that exchanges chemical species through Darcian flow, physical deformation accompanying ice sheet motion, and ionic diffusion (for example, see ref. 49). It would require a till layer less than 2 m thick on average across the entire base of the ice sheet for the porewater reservoir to amount to an additional 10,000 km3 of subglacial storage, assuming reasonable porosity of 35%. Hence, the total subglacial water storage is similar to a few tens of thousands of cubic kilometres. Dividing this volume by the throughflow rate of a few tens of cubic kilometres per year yields an approximate flushing timescale for the modern Antarctic ice sheet of about 1,000 yr. According to Extended Data Fig. 5, such a timescale would allow a build-up of steady-state U234 activity ratios comparable to the ones observed in our samples (thousands of ‰). However, the flushing timescale would have to be lowered by about 2–3 orders of magnitude, to 1–10 years, to bring the δ234USS to values as low as a few hundred ‰. Although, for simplicity, we have focused here on the discussion of the δ234USS, we have also performed calculations of the time evolution of δ234U for a large range of the control parameters f, τf and τw. We find that the flushing timescale is the predominant timescale that controls the rate of δ234U convergence towards its steady-state value. This is particularly the case when the flushing timescale is much shorter than the mean lifetime of 234U (τf ≪ τ4 = 354,260 yr) because the time-dependent, exponential terms in equations (8) and (10) are either dependent on 1/τf or on the sum (1/τf + 1/τ4). When the flushing timescale is short, the 1/τ4 term becomes negligibly small and the evolution of δ234U with time depends only on exponential terms governed by t/τf. This means that a decrease in the flushing timescale to small values, for example, 1–10 yr, from a larger value (for example, between 100 yr and 10,000 yr) would very quickly bring the subglacial δ234U close to its new and lower steady-state value. For instance, δ234U would be within 5% of the steady-state value after only 3–30 yr have elapsed following the decrease of the flushing timescale to 1–10 yr.
There is no reason to suspect that the total volume of water stored beneath the ice sheet was lower by 2–3 orders of magnitude during MIS11 than today. In fact, this volume is unlikely to change much through time and temporal variations in the flushing timescale must be largely controlled by variations in the water throughflow rate, which would have to increase by 2–3 orders of magnitude compared to today to substantially lower subglacial δ234U. Hence, the ice-sheet base would have to be flushed at the rate of approximately 1,000–10,000 km3 per year as compared to the modern rate of around 10 km3 per year. This kind of increase cannot be attributed to an increase in basal melting rate, say, due to ice-sheet thickening during MIS11, which at most could increase the throughflow rate by a small factor, for example, a factor of two. The only process that can introduce enough water to the ice sheet base to lower the flushing timescale by a few orders of magnitude is the penetration of surface meltwater to the ice base through moulins and fractures, as happens on the Greenland Ice Sheet and temperate mountain glaciers50,51. Indeed, two prior studies of δ234U in subglacial waters from beneath Athabasca Glacier and the Greenland Ice Sheet do have very low values, 3–40‰ for the former52 and 5–270‰ for the latter32. The Athabasca Glacier subglacial zone is flushed on seasonal timescales52, whereas the Greenland basins examined in ref. 32 can easily have 0.1–10-yr timescales compatible with the range of values δ234U observed there (Extended Data Fig. 5). In Greenland, however, these observed low δ234U values come from locations where mean annual temperatures in the ablation zone are warmer than −10 °C, whereas most of the EAIS surface is an accumulation zone with mean annual temperatures falling between −30 °C and −50 °C (see ref. 53). Occurrence of sufficient surface melting to cause large enough meltwater penetration to the ice base over current Antarctic accumulation areas would require warming of a few dozen degrees Celsius. Yet the numerical ice-sheet model54 predicts retreat of the ice sheet from subglacial basins such as the Wilkes and Aurora basins with a much smaller thermal forcing accompanying the worst-case Representative Concentration Pathway (RCP8.5) scenario. This indicates that these marine-based regions of the ice sheet will experience grounding-line retreat due to ice–ocean interactions before an ablation zone with high surface melt and substantial water penetration to the bed develops over these regions. Therefore, our favoured interpretation for the low value of δ234U around the time of MIS11 is ice-sheet retreat followed by seawater intrusion into subglacial basins located below sea level rather than a dramatic decrease in the flushing timescale not accompanied by an ice-sheet retreat.
Sample descriptions and field settings
New data presented here are from samples collected from the Pensacola Mountains and the Elephant Moraine, both within East Antarctica. A total of three samples were dated at multiple horizons (PRR16794, PRR50489 and PRR39222). These samples were provided by the Byrd Polar Rock Repository at The Ohio State University55.
Sample PRR16794 at the Pensacola Mountains is entirely calcite and exhibits a fine-scale internal layering related to precipitate growth (Extended Data Fig. 1). The uranium content is 5 ppm. U–Th dates between the top and bottom are within uncertainty at around 200 ka but δ234Ui values are resolvable from top to bottom in the range 1,875–1,990‰ (Supplementary Table 1). The δ18OSMOW of calcite is −9.3‰ (Extended Data Table 2). Sample PRR50489 from the Elephant Moraine consists of inter-bedded calcite and opal, exhibited in discrete layering related to precipitate growth (Extended Data Fig. 2). The δ18OSMOW of the calcite in this sample is −19.87‰ (Extended Data Table 2). The uranium content of calcites are <1 ppm. Opal U concentrations are in the range 10–30 ppm. U–Th dates for opals between the top and bottom of the sample span >100 thousand years in duration and exhibit δ234Ui values of 1,470–2,000‰ (Extended Data Table 1).
Sample PRR39222 from the Elephant Moraine is a precipitate of black calcite. Sample PRR39222 consists of calcite sparite crystals that radiate upwards and out from nucleation surfaces. Organic material is abundant. Silicates are also present but less common. The δ18OSMOW of calcite from this sample is −19.45‰ (Extended Data Table 2). Bulk sample uranium concentrations are <1 ppm and δ234U measured values are in the range 40–140‰ and scale with stratigraphic position in the sample (Extended Data Fig. 3, Extended Data Table 1). The U and Th composition of a calcite digested in 7N HNO3 will represent a mixture of uranium and thorium sourced from the calcite; organics (which are abundant); and U and Th adsorbed onto silicates. Because of adsorbed thorium, we cannot determine a U–Th date and we have therefore restricted our interpretation of PRR39222 to the uranium composition alone. The uranium isotopic composition is also a mixture of the three above sources, but it can be demonstrated that the uranium sourced from the organics or adsorbed onto the surface of detrital silicates is in isotopic equilibrium with the waters that produce the calcite. A definitive test as to whether PRR39222 reliably records subglacial fluid compositions is provided by calcite analysis from sample PRR50489.
Unlike PRR39222, PRR50489 has opals that reliably record the 234U ingrowth within subglacial waters. The calcite measurement from PRR50489 yields values concordant with the values for opal that lie both stratigraphically above and below (Extended Data Table 1). This strongly supports the argument that the bulk calcite digestion, despite having multiple sources of uranium, reliably records the uranium composition of the waters. The calcite from PRR50489 is very similar to PRR39222 and thus can serve as a proxy. Similarities include high Th/U; crystal morphology, of radiating sparite crystals and black colour; and nearly identical δ18O and δ13C values (Extended Data Table 2).
The Elephant Moraine is a supraglacial moraine—an intra-ice site of sediment and rock accumulation of a once deeply residing section of dirty basal ice. The exhumation of this basal ice section occurs as East Antarctic ice flows off the high polar plateau (>2,000 m), and into the western slopes of the Transantarctic Mountains at an elevation of 120 m below the plateau56. As flowing ice interacts with the underlying bedrock topography, this basal layer is transported upwards towards the ice surface56. Surrounding the moraine is a blue-ice area, where there is substantial loss of snow and ice to sublimation. This blue ice is just a small section of a larger sublimation belt that occurs as the thick ice of the EAIS flows eastward and is blocked by the Transantarctic Mountains56. The only exception to EAIS termination within such a sublimation zone is where outlet glaciers are squeezed through the major valleys cutting across the Transantarctic Mountains, such as the Taylor Glacier, which occupies Taylor Valley (see below). The occurrence of upturned ice sections from the base of the EAIS along the western flank of the Transantarctic Mountains is not uncommon. Several such sections25,55,56,57,58, marked by both blue-ice sections bearing meteorites58 as well as exhumed dirty basal ice layers which can contain subglacial precipitates such as those found at Elephant Moraine, Lewis Cliff25 and in proximity to the Pensacola Mountains55 (Fig. 1). The subglacial precipitates that form at the base of the EAIS become frozen into this debris-laden ice layer and are exhumed along with sediments and clasts. Ice ablation at the surface leaves the precipitate samples ‘stranded’. The precipitates are relatively rare compared to other lithologies. It has been suggested by Taylor59 and reviewed by Faure and Mensing56 that the timing of supraglacial moraine inception is directly linked with the timing of thinning of the EAIS. These authors hypothesized that if East Antarctica were thicker, the ice flowing over the bedrock protrusion beneath the Elephant Moraine would have a more muted surface expression than that of a supraglacial moraine. Under this thick-ice condition, the underlying topography would induce an inflection in the ice surface but would be limited to producing a ‘ramp’ that may have crevasses and ice pinnacles at its crest. Under such thick-ice conditions, the EAIS dirty basal ice would not reach the surface. If the ice were to thin in response to climate, the exhumed basal ice would intersect the surface, initiating the formation of the supraglacial moraine. As such, an estimate on the timing of ice thinning can be constrained by estimates of the duration for which morainal materials have resided there, which is provided by exposure dating. Terrestrial ages exist for meteorites found within proximity (<1 km) of the moraine in blue-ice areas. The longest-exposed meteorite dates to 370 ka (ref. 60), suggesting that the Elephant Moraine and the thinning of EAIS ice initiated no sooner than the very end of the MIS11 boundary.
The McMurdo Dry Valleys are the largest rock oasis of Antarctica, where land-terminating glaciers permit subglacial brines to emanate onto the surface or into proglacial lakes11. Taylor Valley, one of the McMurdo Dry Valleys, is occupied by Taylor Glacier, an outlet glacier of the EAIS, and is one of the many narrow mountain passes through which the EAIS extrudes as it flows from the high polar plateau towards the coast. Subglacial discharge reaches the surface at the snout of Taylor Glacier. There hypersaline fluids emanate seasonally in what is referred to as ‘Blood Falls’ owing to the iron oxides that form upon oxidation of soluble iron10,12,61. Subglacial discharge of brines is also detected, geochemically at depth within the proglacial lake (Lake Bonney) that abuts Taylor Glacier8,62. Surveys using airborne transient electromagnetics to image resistivity identify high-solute liquids connecting Lake Bonney to a subglacial region that extends up-glacier for kilometres until increased ice thickness prevents further detection11. It has been speculated that these fluids extend the length of Taylor Glacier back to the EAIS11. The δ234U composition of subglacial discharge in Taylor Valley is in the range 3,500–5,000‰ (Fig. 1, 3)8,10. Similarly 234U-enriched waters are observed in groundwater-fed lakes in Wright Valley, immediately to the north of Taylor Valley8, suggesting that such subglacial discharge has a role in the formation and composition of these lakes as well. Such an observation suggests a shared source for Wright Valley and Taylor Valley fluids and supports speculation that all McMurdo Dry Valleys fluids are sourced from beneath the EAIS. This fuels further speculation that such fluids occur throughout the EAIS but are more readily observed in locations where glaciers terminate on land. Within the McMurdo Dry Valleys lakes, Holocene age carbonates record δ234U compositions similar to modern waters9. Similar lakes are theorized to occupy Taylor Valley at each interglacial period over the past 350 kyr or so9. As discussed in the main text, the δ234U composition of these past carbonates reflects an origination from a 234U-enriched subglacial reservoir and that this reservoir increases in 234U with time, suggesting a coevolution with fluids within the Wilkes Basin. In addition to the age constraints provided by the apparent 234U ingrowth record (Fig. 3), noble gas measurements from the deep waters of the modern Lake Bonney fed by subglacial discharge11 provide additional age constraints. Excess in both 4He and 40Ar up to 200× atmospheric values point to fluid isolation from the atmosphere and contact with rock on durations that exceed 200 kyr (refs. 29,30). This is a minimum estimate, as any dilution by surface waters that exist in the shallow waters of Lake Bonney would yield an apparently younger date. Although these authors suggest that such isolation occurred in situ within Lake Bonney, a compelling documentation for glacial advance and retreat on glacial–interglacial timescales9,63,64 that implies that Taylor Glacier at times occupied the extent of Taylor Valley and reached the Ross Sea suggests that Lake Bonney is an ephemeral feature. In short, these waters did not reside in Lake Bonney for 200 kyr because Lake Bonney did not exist at that time and was filled by ice during the documented expansions of Taylor Glacier. The detection of subglacial discharge beneath Taylor Glacier provides a solution11—the long-term isolation of fluids occurred not in Lake Bonney but beneath the EAIS before their passage beneath Taylor Glacier and into the proglacial Lake Bonney.
Data availability
All data used are included within the Extended Data Tables 1–4 and Extended Data Figs. 1–5 and uploaded to https://doi.org/10.26022/IEDA/111548.
Code availability
Any codes used are available upon request.
References
Dutton, A. et al. Sea-level rise due to polar ice-sheet mass loss during past warm periods. Science 349, aaa4019 (2015).
Lisiecki, L. E. & Raymo, M. E. A Pliocene-Pleistocene stack of 57 globally distributed benthic δ18O records. Paleoceanogr. Paleoclimatol. 20, PA1003 (2005).
Raymo, M. E. & Mitrovica, J. X. Collapse of polar ice sheets during the stage 11 interglacial. Nature 483, 453–456 (2012).
Sugden, D. E., Marchant, D. R. & Denton, G. H. The case for a stable East Antarctic ice sheet: the background. Geogr. Ann. Ser. A 75, 151–154 (1993).
Sugden, D. E. et al. Preservation of Miocene glacier ice in East Antarctica. Nature 376, 412–414 (1995).
Refsnider, K. A. et al. Subglacial carbonates constrain basal conditions and oxygen isotopic composition of the Laurentide Ice Sheet over Arctic Canada. Geology 40, 135–138 (2012).
Chen, T. et al. Ocean mixing and ice-sheet control of seawater 234U/238U during the last deglaciation. Science 354, 626–629 (2016).
Henderson, G. M., Hall, B. L., Smith, A. & Robinson, L. F. Control on (234U/238U) in lake water: a study in the Dry Valleys of Antarctica. Chem. Geol. 226, 298–308 (2006).
Hendy, C. H., Healy, T. R., Rayner, E. M., Shaw, J. & Wilson, A. T. Late Pleistocene glacial chronology of the Taylor Valley, Antarctica, and the global climate. Quat. Res. 11, 172–184 (1979).
Lyons, W. B. et al. The geochemistry of englacial brine from Taylor Glacier, Antarctica. J. Geophys. Res. Biogeosci. 124, 633–648 (2019).
Mikucki, J. A. et al. Deep groundwater and potential subsurface habitats beneath an Antarctic dry valley. Nat. Commun. 6, 6831 (2015).
Mikucki, J. A. & Priscu, J. C. Bacterial diversity associated with Blood Falls, a subglacial outflow from the Taylor Glacier, Antarctica. Appl. Environ. Microbiol. 73, 4029–4039 (2007).
Mengel, M. & Levermann, A. Ice plug prevents irreversible discharge from East Antarctica. Nat. Clim. Chang. 4, 451–455 (2014).
DeConto, R. M. & Pollard, D. Contribution of Antarctica to past and future sea-level rise. Nature 531, 591–597 (2016).
Gasson, E., DeConto, R. & Pollard, D. Antarctic bedrock topography uncertainty and ice sheet stability. Geophys. Res. Lett. 42, 5372–5377 (2015).
Huybrechts, P. Glaciological modelling of the Late Cenozoic East Antarctic ice sheet: stability or dynamism? Geogr. Ann. Ser. A 75, 221–238 (1993).
Wilson, D. J. et al. Ice loss from the East Antarctic Ice Sheet during late Pleistocene interglacials. Nature 561, 383–386 (2018).
Kigoshi, K. Alpha-recoil thorium-234: dissolution into water and the uranium-234/uranium-238 disequilibrium in nature. Science 173, 47–48 (1971).
Hallet, B. Deposits formed by subglacial precipitation of CaCO3. Geol. Soc. Am. Bull. 87, 1003–1015 (1976).
Faure, G., Hoefs, J., Jones, L. M., Curtis, J. B. & Pride, D. E. Extreme 18O depletion in calcite and chert clasts from the Elephant Moraine on the East Antarctic ice sheet. Nature 332, 352–354 (1988).
Hallet, B. Subglacial silica deposits. Nature 254, 682–683 (1975).
Blackburn, T. et al. Composition and formation age of amorphous silica coating glacially polished surfaces. Geology 47, 347–350 (2019).
Aharon, P. Oxygen, carbon and U-series isotopes of aragonites from Vestfold Hills, Antarctica: clues to geochemical processes in subglacial environments. Geochim. Cosmochim. Acta 52, 2321–2331 (1988).
Frisia, S. et al. The influence of Antarctic subglacial volcanism on the global iron cycle during the Last Glacial Maximum. Nat. Commun. 8, 15425 (2017).
Fitzpatrick, J. J., Muhs, D. R. & Jull, A. J. T. Saline minerals in the Lewis Cliff ice tongue, Buckley Island quadrangle, Antarctica. Contrib. Antarctic Res. I 50, 57–69 (1990).
Goodwin, I. D. et al. Modern to Glacial age subglacial meltwater drainage at Law Dome, coastal East Antarctica from topography, sediments and jökulhlaup observations. Geol. Soc. Lond. Spec. Publ. 461, 215–230 (2018).
Chutcharavan, P. M., Dutton, A. & Ellwood, M. J. Seawater 234U/238U recorded by modern and fossil corals. Geochim. Cosmochim. Acta 224, 1–17 (2018).
Berry Lyons, W., Frape, S. K. & Welch, K. A. History of McMurdo Dry Valley lakes, Antarctica, from stable chlorine isotope data. Geology 27, 527–530 (1999).
Poreda, R. J., Hunt, A. G., Lyons, W. B. & Welch, K. A. The helium isotopic chemistry of Lake Bonney, Taylor Valley, Antarctica: timing of late Holocene climate change in Antarctica. Aquat. Geochem. 10, 353–371 (2004).
Warrier, R. B., Castro, M. C., Hall, C. M., Kenig, F. & Doran, P. T. Reconstructing the evolution of Lake Bonney, Antarctica using dissolved noble gases. Appl. Geochem. 58, 46–61 (2015).
Pogge von Strandmann, P. A. E. et al. Riverine behaviour of uranium and lithium isotopes in an actively glaciated basaltic terrain. Earth Planet. Sci. Lett. 251, 134–147 (2006).
Arendt, C. A. et al. Influence of glacial meltwater on global seawater δ234U. Geochim. Cosmochim. Acta 225, 102–115 (2018).
Bard, E., Fairbanks, R. G., Hamelin, B., Zindler, A. & Hoang, C. T. Uranium-234 anomalies in corals older than 150,000 years. Geochim. Cosmochim. Acta 55, 2385–2390 (1991).
Catania, G. A., Neumann, T. A. & Price, S. F. Characterizing englacial drainage in the ablation zone of the Greenland ice sheet. J. Glaciol. 54, 567–578 (2008).
Bøggild, C. E., Brandt, R. E., Brown, K. J. & Warren, S. G. The ablation zone in northeast Greenland: ice types, albedos and impurities. J. Glaciol. 56, 101–113 (2010).
Yamane, M. et al. Exposure age and ice-sheet model constraints on Pliocene East Antarctic ice sheet dynamics. Nat. Commun. 6, 7016 (2015).
Reyes, A. V. et al. South Greenland ice-sheet collapse during marine isotope stage 11. Nature 510, 525–528 (2014).
Gomez, N., Mitrovica, J. X., Tamisiea, M. E. & Clark, P. U. A new projection of sea level change in response to collapse of marine sectors of the Antarctic Ice Sheet. Geophys. J. Int. 180, 623–634 (2010).
Fretwell, P. et al. Bedmap2: improved ice bed, surface and thickness datasets for Antarctica. Cryosphere 7, 375–393 (2013).
Greene, C. A., Gwyther, D. E. & Blankenship, D. D. Antarctic Mapping Tools for Matlab. Comput. Geosci. 104, 151–157 (2017).
Pattyn, F. Antarctic subglacial conditions inferred from a hybrid ice sheet/ice stream model. Earth Planet. Sci. Lett. 295, 451–461 (2010).
Condon, D. J., McLean, N., Noble, S. R. & Bowring, S. A. Isotopic composition (238U/235U) of some commonly used uranium reference materials. Geochim. Cosmochim. Acta 74, 7127–7143 (2010).
Hamelin, B., Bard, E., Zindler, A. & Fairbanks, R. G. 234U/238U mass spectrometry of corals: how accurate is the U–Th age of the last interglacial period? Earth Planet. Sci. Lett. 106, 169–180 (1991).
Cheng, H. et al. Improvements in 230Th dating, 230Th and 234U half-life values, and U–Th isotopic measurements by multi-collector inductively coupled plasma mass spectrometry. Earth Planet. Sci. Lett. 371/372, 82–91 (2013).
Andersen, M. B., Erel, Y. & Bourdon, B. Experimental evidence for 234U–238U fractionation during granite weathering with implications for 234U/238U in natural waters. Geochim. Cosmochim. Acta 73, 4124–4141 (2009).
Prentice, M. L. & Matthews, R. K. Tertiary ice sheet dynamics: the snow gun hypothesis. J. Geophys. Res. Solid Earth 96, 6811–6827 (1991).
Christoffersen, P., Bougamont, M., Carter, S. P., Fricker, H. A. & Tulaczyk, S. Significant groundwater contribution to Antarctic ice streams hydrologic budget. Geophys. Res. Lett. 41, 2003–2010 (2014).
Dowdeswell, J. A. & Siegert, M. J. Ice-sheet numerical modeling and marine geophysical measurements of glacier-derived sedimentation on the Eurasian Arctic continental margins. Geol. Soc. Am. Bull. 111, 1080–1097 (1999).
Tulaczyk, S., Kamb, B. & Engelhardt, H. F. Estimates of effective stress beneath a modern West Antarctic ice stream from till preconsolidation and void ratio. Boreas 30, 101–114 (2001).
Howat, I. M., Joughin, I., Tulaczyk, S. & Gogineni, S. Rapid retreat and acceleration of Helheim Glacier, east Greenland. Geophys. Res. Lett. 32, L22502 (2005).
Howat, I. M., Tulaczyk, S., Waddington, E. & Björnsson, H. Dynamic controls on glacier basal motion inferred from surface ice motion. J. Geophys. Res. Earth Surf. 113, F03015 (2008).
Arendt, C. A., Aciego, S. M., Sims, K. W. W. & Aarons, S. M. Seasonal progression of uranium series isotopes in subglacial meltwater: implications for subglacial storage time. Chem. Geol. 467, 42–52 (2017).
Bréant, C., Martinerie, P., Orsi, A., Arnaud, L. & Landais, A. Modelling firn thickness evolution during the last deglaciation: constraints on sensitivity to temperature and impurities. Clim. Past 13, 833–853 (2017).
Golledge, N. R. et al. The multi-millennial Antarctic commitment to future sea-level rise. Nature 526, 421–425 (2015).
The Polar Rock Repository. Archive of information about geological samples available for research from the Ohio State University Byrd Polar and Climate Research Center (BPCRC) Polar Rock Repository https://data.nodc.noaa.gov/cgi-bin/iso?id=gov.noaa.ngdc.mgg.geology:archived-data_BPCRC-polar-rock-repository (NOAA National Centers for Environmental Information, 2019).
Faure, G. & Mensing, T. M. The Transantarctic Mountains: Rocks, Ice, Meteorites And Water (Springer Science & Business Media, 2010).
Faure, G. & Taylor, K. S. The geology and origin of the Elephant Moraine on the East Antarctic Ice Sheet. Antarct. J. US 20, 11 (1985).
Cassidy, W., Harvey, R., Schutt, J., Delisle, G. & Yanai, K. The meteorite collection sites of Antarctica. Meteoritics 27, 490–525 (1992).
Taylor, K. S. Lithologies and Distribution of Clasts in the Elephant Moraine, Allan Hills South Victoria Land, Antarctica. MSc thesis, Kent State Univ. (1986).
Nishiizumi, K., Elmore, D. & Kubik, P. W. Update on terrestrial ages of Antarctic meteorites. Earth Planet. Sci. Lett. 93, 299–313 (1989).
Lyons, W. B. et al. Halogen geochemistry of the McMurdo Dry Valleys lakes, Antarctica: clues to the origin of solutes and lake evolution. Geochim. Cosmochim. Acta 69, 305–323 (2005).
Lyons, W. B. et al. Strontium isotopic signatures of the streams and lakes of Taylor Valley, Southern Victoria Land, Antarctica: chemical weathering in a polar climate. Aquat. Geochem. 8, 75–95 (2002).
Brook, E. J. et al. Chronology of Taylor Glacier advances in Arena Valley, Antarctica, using in situ cosmogenic 3He and 10Be. Quat. Res. 39, 11–23 (1993).
Bockheim, J. G., Prentice, M. L. & McLeod, M. Distribution of glacial deposits, soils, and permafrost in Taylor Valley, Antarctica. Arct. Antarct. Alp. Res. 40, 279–286 (2008).
Acknowledgements
We thank J. Schutt, G. Faure and D. Schmidt for their sample collection at the Elephant Moraine and A. Grunow and the Byrd Polar Rock Repository for providing samples with a ‘PRR’ prefix. We also thank J. Paces, S. Hemming and T. Rasbury for their input. This research was funded by NSF 1644171 to T.B. and S.T.
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T.B. wrote the manuscript, led this study and developed the U-series methods. G.H.E. performed model simulations, tracer calibration and U-series data reduction. S.T. interpreted data and performed modelling. M.S. prepared samples and performed clean laboratory work. G.P. performed clean laboratory work and tracer calibration. N.McL. did the maximum likelihood model construction. B.H. interpreted data. J.C.Z. performed the oxygen isotopic analyses. B.C. did the SEM imaging. J.T.B. prepared samples and performed clean laboratory work.
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Extended data figures and tables
Extended Data Fig. 1 Images of sample PRR16794.
a, b, Sample shown in visible light (with location of dated horizons corresponding to data reported in Extended Data Table 1) (a) and the scanning electron microscope (SEM)/energy-dispersive X-ray spectroscopy (EDS) compositional map showing variations in manganese (green for high Mn, black for low Mn) (b).
Extended Data Fig. 2 Images of sample PRR50489.
a, b, Sample shown in visible light (with location of dated horizons corresponding to data reported in Extended Data Table 1) (a) and the SEM/EDS compositional map showing Ca and Si (b). The sample exhibits an angular unconformity, indicating that the sample physically moved beneath the ice before accumulation began again. Clct, calcite.
Extended Data Fig. 3 Model constraints on 234U ingrowth history of PRR39222.
The inset photograph shows sample PRR39222 under visible light with the location of δ234U measurements marked. The main plot shows the measured δ234U for PRR39222 at three horizons, revealing an increasing δ234U from top to bottom (Extended Data Table 1). Because of the high thorium (Th) contents, we cannot define a formation age and thus cannot identify a reliable δ234Ui. The purple curves in Fig. 3 represent the possible δ234Ui values for the top (higher δ234U) and bottom (lower δ234U) for any formation time. What we do not know is the absolute time at which this sample formed or the duration it formed over. However, we do know that: (1) the δ234Ui for the top and bottom of the sample must lie on these purple lines; (2) the sample must be younger than 1,500 kyr given that the measured δ234U is not in secular equilibrium. In addition to these known conditions, we can assume that the calcite in PRR39222 probably formed very rapidly as indicated by: (1) morphology, specifically radiating clusters of blade-like sparite; (2) lack of unconformities; (3) shared δ18O and δ13C composition with rapidly forming calcite from PRR50489, which is constrained by geochronology. Data from the literature as well as the geochronologic constraints presented in Extended Data Table 1 provide limits on the rate of sub-ice calcite formation (0.5 mm kyr−1 is shallow and 5 mm kyr−1 is steep). Given a known sample dimension of 4.5 cm, any assumed precipitation rate translates to a time duration for sample formation of 10–90 kyr. Assuming these durations, along with the requirement that the bottom and top of the sample intersects the purple curves in Fig. 3, permits us to define possible δ234Ui ingrowth histories (black arrows in Fig. 3). The rate of modelled 234U accumulation as recorded by PRR39222 is strongly controlled by assumed formation age with only a narrow time range yielding 234U ingrowth histories consistent with the other Wilkes Basin fluid histories. For example, if the sample were to have formed at 1,000 ka, we predict a change in δ234Ui of about 300% from the top to the bottom of this sample. Such rapid ingrowth histories result in δ234U compositions that would result in δ234U compositions that far exceeds anything observed in Antarctica (>6,000‰). If, however, the sample were to have formed at about 400 ka, the projected ingrowth histories would match both model projections and measured data for the Wilkes Basin. Only scenarios that place PRR39222 formation at roughly <500 ka yield projected ingrowth histories consistent with the blue curve. In addition to the above analysis, the occurrence of low δ234U (<500‰) in subglacial fluids is apparently rare, having been identified in this region only in samples older than about 300 ka. Collectively, this suggests that the 234U ingrowth history recorded by PRR39222 is at least consistent with formation at about 400 ka.
Extended Data Fig. 4 Long-term results of measurements of NBS 4321 (5.2919 × 10−5 ± 0.013 × 10−5 (0.25%)) at UCSC using an IsotopX X62, TIMS.
All uncertainties are absolute 2σ.
Extended Data Fig. 5 Steady-state activity ratio of 234U and 238U as a function of the flushing timescale for three different values of the 234U ejection factor.
The dotted line shows the assumed level of δ234U in meltwater. The assumed weathering timescale is 100 million years.
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Blackburn, T., Edwards, G.H., Tulaczyk, S. et al. Ice retreat in Wilkes Basin of East Antarctica during a warm interglacial. Nature 583, 554–559 (2020). https://doi.org/10.1038/s41586-020-2484-5
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