Changes in Eastern Pacific ocean ventilation at intermediate depth over the last 150 kyr BP

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Abstract

The circulation patterns of the deep glacial Pacific Ocean are still debated. Difficulties arise due to the scarcity of reliable paleoceanographic records that can document the past movements and properties of Pacific Ocean water masses. Here, we jointly use δ13C and δ18O measured on the epibenthic foraminifer Cibicidoides wuellerstorfi, from the MD02-2529 sediment core collected at 1619 m water depth in the eastern equatorial Pacific, to monitor changes in water mass circulation spanning the past 150 kyr BP. After the extraction of short-term (centennial to millennial-scale) δ13C and δ18O changes, which were ~ 1.0 and 0.5‰, respectively, we observed that these rapid δ13C and δ18O shifts were closely interrelated during the last 150 kyr BP. A comparison of MD02-2529 with other benthic δ13C records localized to the north and south of the core location revealed that MD02-2529 was alternately bathed by a northern nutrient-rich and a southern nutrient-poor water mass. The comparison provided a diagnostic for the latitudinal movements of a sharp water mass front that was particularly evident during marine isotope stages 4 and 3 on the millennial timescale. By considering that δ13C is an indicator of the northern vs. southern origin of the water that bathed the MD02-2529 coring site in the past, we found that a North Pacific water mass, that occasionally spreads to the eastern Pacific Ocean as deep as 1600 m and as far south as 8°N, was responsible for shifts toward the positive δ18O we observed in the past. We then used the δ13C/δ18O relationship to reconstruct latitudinal temperature and/or salinity gradients of the water mass that were linked to changes in the northern and/or the southern water mass end-members. Evolution of the δ13C/δ18O relationship spanning the past 150 kyr BP has shed light on how hydrological processes occurring at northern and southern high latitudes are transmitted to the ocean's interior through water mass advection.

Introduction

Modern deep-water formation sites are localized in the northern North Atlantic and around Antarctica in the Weddell and Ross Seas (Kuhlbrodt et al., 2007), while there is no deep-water formation in the North Pacific. North Atlantic Deep Water (NADW) ventilates most of the present-day deep Atlantic Ocean. The fact that there is no NADW equivalent for the North Pacific makes the present-day Thermohaline Circulation (THC) asymmetric. The absence of North Pacific deep-water formation leads to oxygen depletion between ~ 500 and ~ 2500 m in the entire present-day North Pacific Ocean (Helly and Levin, 2004) (Fig. 1a).

Drastic changes in Pacific Ocean circulation triggered by high-latitude hydrological processes are candidates for explaining part of the observed changes in atmospheric carbon dioxide during the Pleistocene (Haug and Sigman, 2009, Sigman et al., 2010). However, up until now there have not been any simple schemes for how past circulation in the Pacific could have differed from modern circulation. On one hand, an increase in the nutrient content of the deep glacial ocean could suggest that deep Pacific Ocean circulation was reduced (Sigman et al., 2010). On the other hand, Wunsch (2003) argued that reduced circulation during glacial periods is unlikely since increased wind-induced mixing may have favoured enhanced overturning.

Information regarding oceanic geochemistry and the temperature and/or the salinity of past water masses can be extracted from stable isotopes measured on benthic foraminifera tests that are contained in marine sediment cores. The distribution of the δ13C of ΣCO2 in the modern ocean is tightly linked to the oxygen and nutrient content, which are shaped by large-scale oceanic water mass movements (Kroopnick, 1985). Since the δ13C of benthic foraminifera reflects the δ13C of the Dissolved Inorganic Carbon (DIC) in seawater, past changes in the seawater oxygen and/or nutrient content can be reconstructed using the δ13C obtained from benthic foraminifera tests in deep-sea sediments (Duplessy et al., 1984). On the other hand, the δ18O of seawater (δ18Osw) is related to salinity (Delaygue et al., 2000), and past changes in δ18Osw can be monitored using benthic foraminifera δ18O (Zahn et al., 1991, Lynch-Stieglitz et al., 1999). However, the temperature fractionation that modulates the difference between the δ18Osw and the δ18O of foraminifer tests, makes foraminifera δ18O values a mixed signal for both temperature and δ18Osw (salinity).

The work described here makes a first attempt to jointly use benthic foraminifera δ13C and δ18O signatures in order to combine the information provided by each independently. We present a new high-resolution record of stable isotope measurements performed on epibenthic foraminifera that were obtained from a marine sediment core located in the Panama Basin (core MD02-2529, 08°12.33′N; 84°07.32′W; 1619 m water depth) that spans the past 150 kyr BP. The eastern equatorial Pacific (EEP) is situated at the confluence of northern suboxic and southern oxic waters at intermediate depths (Fig. 1). Therefore, studying past changes in water mass properties from this region will provide insights regarding how the North Pacific shadow zone has evolved in the past.

Section snippets

Modern-day Pacific Ocean circulation

In the modern North Pacific Ocean, relatively low sea surface salinities restrict North Pacific Intermediate Water (NPIW) formation to the upper 500 m of water depth (Warren, 1983, Talley, 1993; Reid, 1997; Emile-Geay et al., 2003, Fig. 1). Waters flowing below this depth have a remote southern component composed of a mixture of both NADW and waters originating from the Southern Ocean, at both intermediate (the Antarctic Intermediate Water, AAIW) and abyssal depths (the Antarctic Bottom Water,

Pacific Ocean paleoceanography deduced from benthic δ13C and δ18O

For the Last Glacial Maximum (LGM) time slice a deconvolution of temperature and salinity can be performed using an analysis of sedimentary pore water, for which salinity (chlorinity) together with benthic foraminifera stable isotopes and pore water δ18Osw measurements provide temperature and salinity estimations (Adkins et al., 2002). Such an analysis was performed on sediments collected from different oceanic basins and indicated that the deep ocean was uniformly cold, but that sharp salinity

Methods

We measured stable carbon and oxygen isotopes on the benthic foraminifer species Cibicidoides wuellerstorfi, and on the planktonic foraminifera species Globigerinoides ruber and Neogloboquadrina dutertrei in the > 250 μm size fraction in MD02-2529 core. Samples containing one to four benthic foraminifera and two to six planktonic foraminifera were treated with H3PO4 at 70 °C. The resulting CO2 was analysed using a Finnigan Delta Advantage mass spectrometer at CEREGE. We performed ~ 20 replicates on

Patterns and significance of the C. wuellerstorfi isotopic signatures

With epibenthic foraminifera considered as oxic taxa (see e.g. Jorissen, 1999), the presence of C. wuellerstorfi throughout the sedimentary sequence indicates that bottom water oxygen concentrations never reached dysoxic values over the time interval studied (Fig. 2). The δ18O of C. wuellerstorfi18OCw) for the last 10 kyr BP was ~ 2.6 ± 0.1‰ (Fig. 2). Between 10 and 20 kyr BP, the last glacial termination was marked by a δ18OCw increase of ~ 2‰ (Fig. 2). MIS2 values of benthic δ18O remained rather

The origin and extent of glacial EEP water masses at mid-depth

One valid explanation for long-term and rapid variations in δ13CCw recorded during the last glacial period in core MD02-2529 potentially lies in long-term and rapid movements of a sharp water mass front located in the vicinity of the coring site at approximately 1600 m water depth. To test this hypothesis we first compared epibenthic foraminiferal δ13C records available from the north and the south of the MD02-2529 core location in the 1400 to 1800 m water depth range (Fig. 1).

The sediment core

Conclusions

We measured stable isotopes on benthic foraminifera from the MD02-2529 marine sediment core collected in Panama Basin at ~ 1600 m water depth, which spans the last 150 kyr BP. The δ13CCw record is characterized by relatively stable and high values for the last 25 kyr BP, as compared to earlier time periods when δ13CCw values were more variable at millennial and longer timescales. We found that millennial-scale δ13CCw anomalies prior to 25 kyr BP were negatively correlated with millennial-scale δ18OCw

Acknowledgements

We thank Frauke Rostek for measuring alkenones and Corinne Sonzogni for performing the stable isotope analyses. We thank Jess Adkins, Alan Mix, Olivier Marchal, Rainer Zahn, and Cécile Blanchet for the discussions and advices. We thank Yiming Wang for the English language editing. The quality of the manuscript was substantially improved by the constructive comments of Peter deMenocal and two anonymous reviewers.

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      In synchrony with the Dansgaard-Oeschger cycles, the circulation cell of the North Pacific at intermediate depth intensified and expanded during the cold stages of the last glacial period with a larger dominance of the Pacific Intermediate Water mass (Keigwin, 1998); while the flow of the Southern Component water (i.e., Antarctic Intermediate Water) arrived during interstadials, but contracted to the South during stadials (Hendy and Kennett, 2003; Erdem et al., 2020). Vigorous circulation at intermediate depths in the Southern Ocean has explained the millennial scale variability observed in the sedimentary record of the Northeast Pacific (Hendy and Kennett, 2003; Leduc et al., 2010; Cartapanis et al., 2011). The millennial scale variability of δ13CU (Fig. 6A) from the Magdalena margin, Baja California, was contrasted with the δ13C of core ODP Site 1014 (Fig. 6A) (sensitive to the NPIW mode of the Californian margin; Stott et al., 2000) and MD02-2529 (Fig. 6A) (sensitive to the AAIW mode of the Panama basin; Leduc et al., 2010), as well as the end-members of the Southern Ocean (Fig. 6A, SO213/2-84-1; Ronge et al., 2015) and the North Pacific (Fig. 6A, SO201-2-101 KL; Max et al., 2017).

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