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  <front>
    <journal-meta><journal-id journal-id-type="publisher">CP</journal-id><journal-title-group>
    <journal-title>Climate of the Past</journal-title>
    <abbrev-journal-title abbrev-type="publisher">CP</abbrev-journal-title><abbrev-journal-title abbrev-type="nlm-ta">Clim. Past</abbrev-journal-title>
  </journal-title-group><issn pub-type="epub">1814-9332</issn><publisher>
    <publisher-name>Copernicus Publications</publisher-name>
    <publisher-loc>Göttingen, Germany</publisher-loc>
  </publisher></journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.5194/cp-17-2091-2021</article-id><title-group><article-title>Climate, cryosphere and carbon cycle controls on Southeast Atlantic
orbital-scale carbonate deposition since the<?xmltex \hack{\break}?> Oligocene (30–0 Ma)</article-title><alt-title>Controls and orbital pacing of Southeast Atlantic carbonate deposition (30–0 Ma)​​​​​​​</alt-title>
      </title-group><?xmltex \runningtitle{Controls and orbital pacing of Southeast Atlantic carbonate deposition (30--0\,Ma)​​​​​​​}?><?xmltex \runningauthor{A. J. Drury et al.}?>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes" rid="aff1 aff2">
          <name><surname>Drury</surname><given-names>Anna Joy</given-names></name>
          <email>ajdrury@marum.de</email><email>a.j.drury@ucl.ac.uk</email>
        <ext-link>https://orcid.org/0000-0001-6206-7284</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Liebrand</surname><given-names>Diederik</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-6925-7889</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Westerhold</surname><given-names>Thomas</given-names></name>
          
        <ext-link>https://orcid.org/0000-0001-8151-4684</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3">
          <name><surname>Beddow</surname><given-names>Helen M.</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff4">
          <name><surname>Hodell</surname><given-names>David A.</given-names></name>
          
        <ext-link>https://orcid.org/0000-0001-8537-1588</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Rohlfs</surname><given-names>Nina</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff5">
          <name><surname>Wilkens</surname><given-names>Roy H.</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-4844-1046</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff6">
          <name><surname>Lyle</surname><given-names>Mitchell</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-0861-0511</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff7">
          <name><surname>Bell</surname><given-names>David B.</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff7">
          <name><surname>Kroon</surname><given-names>Dick</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Pälike</surname><given-names>Heiko</given-names></name>
          
        <ext-link>https://orcid.org/0000-0003-3386-0923</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3">
          <name><surname>Lourens</surname><given-names>Lucas J.</given-names></name>
          
        </contrib>
        <aff id="aff1"><label>1</label><institution>MARUM – Center for Marine Environmental Sciences, University of Bremen, Leobener Strasse 8, 28359 Bremen, Germany</institution>
        </aff>
        <aff id="aff2"><label>2</label><institution>Department of Earth Sciences, University College London, Gower Street, London, WC1E 6BT, UK</institution>
        </aff>
        <aff id="aff3"><label>3</label><institution>Department of Earth Sciences, Faculty of Geosciences, Utrecht
University, Utrecht, the Netherlands</institution>
        </aff>
        <aff id="aff4"><label>4</label><institution>Department of Earth Science, University of Cambridge, Cambridge, EH9 3FE, UK</institution>
        </aff>
        <aff id="aff5"><label>5</label><institution>School of Ocean and Earth Science and Technology, University of Hawaii, Honolulu, Hawaii 96822, USA</institution>
        </aff>
        <aff id="aff6"><label>6</label><institution>College of Earth, Ocean, and Atmospheric Science, Oregon State
University, Corvallis, Oregon 97331, USA</institution>
        </aff>
        <aff id="aff7"><label>7</label><institution>School of GeoSciences, University of Edinburgh, Edinburgh, CB2 3EQ, UK</institution>
        </aff>
      </contrib-group>
      <author-notes><corresp id="corr1">Anna Joy Drury (ajdrury@marum.de, a.j.drury@ucl.ac.uk)</corresp></author-notes><pub-date><day>15</day><month>October</month><year>2021</year></pub-date>
      
      <volume>17</volume>
      <issue>5</issue>
      <fpage>2091</fpage><lpage>2117</lpage>
      <history>
        <date date-type="received"><day>5</day><month>August</month><year>2020</year></date>
           <date date-type="rev-request"><day>4</day><month>September</month><year>2020</year></date>
           <date date-type="rev-recd"><day>29</day><month>May</month><year>2021</year></date>
           <date date-type="accepted"><day>15</day><month>June</month><year>2021</year></date>
      </history>
      <permissions>
        <copyright-statement>Copyright: © 2021 </copyright-statement>
        <copyright-year>2021</copyright-year>
      <license license-type="open-access"><license-p>This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this licence, visit <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link></license-p></license></permissions><self-uri xlink:href="https://cp.copernicus.org/articles/.html">This article is available from https://cp.copernicus.org/articles/.html</self-uri><self-uri xlink:href="https://cp.copernicus.org/articles/.pdf">The full text article is available as a PDF file from https://cp.copernicus.org/articles/.pdf</self-uri>
      <abstract><title>Abstract</title>
    <p id="d1e225">The evolution of the Cenozoic cryosphere from unipolar to
bipolar over the past 30 million years (Myr) is broadly known. Highly
resolved records of carbonate (CaCO<inline-formula><mml:math id="M1" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>) content provide insight into the
evolution of regional and global climate, cryosphere, and carbon cycle
dynamics. Here, we generate the first Southeast Atlantic CaCO<inline-formula><mml:math id="M2" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content
record spanning the last 30 Myr, derived from X-ray fluorescence (XRF)
ln(Ca <inline-formula><mml:math id="M3" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) data collected at Ocean Drilling Program Site 1264 (Walvis Ridge,
SE Atlantic Ocean). We present a comprehensive and continuous depth and age
model for the entirety of Site 1264 (<inline-formula><mml:math id="M4" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 316 m; 30 Myr). This
constitutes a key reference framework for future palaeoclimatic and
palaeoceanographic studies at this location. We identify three phases with
distinctly different orbital controls on Southeast Atlantic CaCO<inline-formula><mml:math id="M5" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
deposition, corresponding to major developments in climate, the cryosphere
and the carbon cycle: (1) strong <inline-formula><mml:math id="M6" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity pacing
prevails during Oligocene–Miocene global warmth (<inline-formula><mml:math id="M7" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 30–13 Ma), (2) increased eccentricity-modulated precession pacing appears after the middle Miocene Climate Transition (mMCT) (<inline-formula><mml:math id="M8" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 14–8 Ma), and (3) pervasive
obliquity pacing appears in the late Miocene (<inline-formula><mml:math id="M9" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 7.7–3.3 Ma)
following greater importance of high-latitude processes, such as increased
glacial activity and high-latitude cooling. The lowest CaCO<inline-formula><mml:math id="M10" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content
(92 %–94 %) occurs between 18.5 and 14.5 Ma, potentially reflecting dissolution
caused by widespread early Miocene warmth and preceding Antarctic
deglaciation across the Miocene Climatic Optimum (<inline-formula><mml:math id="M11" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 17–14.5 Ma)
by 1.5 Myr. The emergence of precession pacing of CaCO<inline-formula><mml:math id="M12" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition at
Site 1264 after <inline-formula><mml:math id="M13" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 14 Ma could signal a reorganisation of
surface and/or deep-water circulation in this region following Antarctic
reglaciation at the mMCT. The increased sensitivity to precession at Site 1264 between 14 and 13 Ma is associated with an increase in mass accumulation
rates (MARs) and reflects increased regional CaCO<inline-formula><mml:math id="M14" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> productivity and/or
recurrent influxes of cooler, less corrosive deep waters. The highest
carbonate content (%CaCO<inline-formula><mml:math id="M15" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>) and MARs indicate that the late Miocene–early Pliocene Biogenic
Bloom (LMBB) occurs between <inline-formula><mml:math id="M16" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.8 and 3.3 Ma at Site 1264; broadly
contemporaneous with the LMBB in the equatorial Pacific Ocean. At Site 1264,
the onset of the LMBB roughly coincides with appearance of strong obliquity
pacing of %CaCO<inline-formula><mml:math id="M17" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>, reflecting increased high-latitude forcing. The
global expression of the LMBB may reflect increased nutrient input into the
global ocean resulting from enhanced aeolian dust and/or glacial/chemical
weathering fluxes, due to enhanced glacial activity and increased meridional
temperature gradients. Regional variability in the<?pagebreak page2092?> timing and amplitude of
the LMBB may be driven by regional differences in cooling, continental
aridification and/or changes in ocean circulation in the late Miocene.</p>
  </abstract>
    </article-meta>
  </front>
<body>
      

<sec id="Ch1.S1" sec-type="intro">
  <label>1</label><title>Introduction</title>
      <p id="d1e374">Over the last 30 million years (Myr), Earth's climate system evolved
considerably from the early unipolar Antarctic Coolhouse to our modern-day
Icehouse world
(Zachos
et al., 2001; De Vleeschouwer et al., 2017, 2020; Littler et al., 2019;
Westerhold et al., 2020). Inferred from benthic foraminiferal oxygen isotope
data (<inline-formula><mml:math id="M18" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O), the Oligocene–early Miocene (30–17 million years
ago [Ma]) was characterised by variable Antarctic ice volumes
(Liebrand et al., 2017).
This unipolar Coolhouse was marked by high-amplitude glacial–interglacial
cycles that were predominantly eccentricity paced
(Wade and Pälike,
2004; Pälike et al., 2006; Liebrand et al., 2016, 2017; Beddow et al.,
2018). During the warm Miocene Climatic Optimum (MCO; 17–14.7 Ma), the
Antarctic ice sheet shrank relative to its early Miocene size
(Shevenell
et al., 2004, 2008; Holbourn et al., 2015; Gasson et al., 2016; Levy et al.,
2016), before prevalent unipolar conditions were re-established when
Antarctica reglaciated across the middle Miocene Climate Transition (mMCT)
around <inline-formula><mml:math id="M19" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 13.9 Ma (Shevenell
et al., 2004, 2008; Holbourn et al., 2005, 2014; Levy et al., 2016).
Following the onset of strong obliquity pacing at <inline-formula><mml:math id="M20" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.7 Ma (Drury
et al., 2017, 2018b) and further global cooling during the late
Miocene–early Pliocene (7–5 Ma, Herbert et al.,
2016), a fully bipolar Icehouse world was established at <inline-formula><mml:math id="M21" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 2.7 Ma
(Bailey et al., 2013).</p>
      <p id="d1e409">High-resolution carbonate records provide insight into past dynamics and
long-term evolution of Earth's climate and carbon cycle. Carbonate
deposition is largely controlled by a combination of the amount of biogenic
carbonate productivity in the surface waters and the degree of dissolution
in the water column and/or seafloor, as well as sedimentary processes such
as winnowing and dilution (Berger,
1970; Van Andel et al., 1975; Lyle et al., 1995, 2019; Lyle, 2003;
Pälike et al., 2012). Primary and export productivity are sensitive
recorders of past climate variability, responding to changes in solar
insolation and nutrient availability (Coxall
and Wilson, 2011; Pälike et al., 2012; Lyle and Baldauf, 2015; Carter et
al., 2016; Liebrand et al., 2018). Dissolution at the seafloor is primarily
driven by regional changes in the lysocline and carbonate compensation
depth, with less carbonate preserving at greater depths and/or in areas
with corrosive bottom waters
(Berger,
1970; Van Andel et al., 1975; Lyle et al., 2019). Changes in deep-sea
currents can alter the composition of the sediment through processes like
winnowing or dilution, which respectively remove fine-grained material or
increase certain sedimentary components relative to others (e.g. increased
dilution with terrigenous material). Understanding past changes in carbonate
deposition can inform about past climate development by helping to
disentangle how global processes affected regional production and deposition
of biogenic carbonates. Deep marine carbonate variability in the Equatorial
Pacific Ocean is well documented for the Cenozoic (Van
Andel et al., 1975; Lyle, 2003; Pälike et al., 2012; Lyle and Baldauf,
2015; Kochhann et al., 2016; Beddow et al., 2018; Lyle et al., 2019).
However, relatively few Atlantic records of comparable quality, resolution
and extent exist (e.g.
Liebrand et al., 2016), limiting our understanding of the palaeoceanographic
evolution of this basin. Improving our understanding of the Southeast
Atlantic Ocean, including the Angola Basin, is of particular interest, as
the water column structure and surface and deep-water ocean circulation in
this region were affected by palaeoceanographic conditions in both the North
Atlantic Ocean and Southern Ocean (Seidov and Maslin, 2001;
Bell et al., 2015).</p>
      <p id="d1e412">Here, we present the first astronomically tuned record of Southeast
Atlantic carbonate deposition spanning the last 30 Myr at orbital-scale
resolution. We use expanded deep-sea sedimentary sequences from Ocean
Drilling Program (ODP) Site 1264 (Leg 208; Shipboard
Scientific Party Leg 208, 2004a), located on the Angola Basin side of Walvis
Ridge. New high-resolution X-ray fluorescence (XRF) core-scanning data is
collected for the middle Miocene–present sediments at ODP Site 1264, which is
integrated with published Oligocene–early Miocene XRF data from ODP Sites 1264 and 1265
(Liebrand
et al., 2016). The XRF ln(Ca <inline-formula><mml:math id="M22" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) data are used to verify, update and revise
the composite depth scale and splice at Site 1264 to form a continuous
315.96 m record. Carbonate content (%CaCO<inline-formula><mml:math id="M23" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>) is estimated using the
XRF ln(Ca <inline-formula><mml:math id="M24" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) data. We generate an astrochronology between 3 and 17 Ma using the new %CaCO<inline-formula><mml:math id="M25" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data, which is integrated with published
Oligocene–early Miocene and Plio-Pleistocene age models (Bell
et al., 2014; Liebrand et al., 2016). The resulting high-resolution records
will help determine shifts in the orbital pacing of Southeast Atlantic
CaCO<inline-formula><mml:math id="M26" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition in relation to the broader climatic trends of the last
30 Myr. We investigate how widespread Miocene warmth followed by Antarctic
glaciation influenced the pacing and preservation of Southeast Atlantic
carbonate deposition. Finally, we establish the relative timing of the late
Miocene–early Pliocene Biogenic Bloom (LMBB; acronym from Lyle et al., 2019)
in the Southeast Atlantic Ocean versus Pacific Ocean and explore what this
reveals about the global and regional driving forces of this
multi-million-year productivity event.</p>
</sec>
<sec id="Ch1.S2">
  <label>2</label><title>Materials and methods</title>
<sec id="Ch1.S2.SS1">
  <label>2.1</label><title>ODP Sites 1264 and 1265</title>
      <p id="d1e471">This study utilises material recovered at ODP Site 1264 on the Angola Basin
side of Walvis Ridge in the Southeast Atlantic (Fig. 1; 28<inline-formula><mml:math id="M27" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>31.955<inline-formula><mml:math id="M28" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula> S, 2<inline-formula><mml:math id="M29" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>50.730<inline-formula><mml:math id="M30" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula> E, 2505 m water depth; Shipboard Scientific Party Leg 208, 2004a), which<?pagebreak page2093?> was drilled during ODP Leg 208 to provide a Cenozoic deep-sea record of the South Atlantic
(Shipboard Scientific Party Leg 208, 2004a, b). At Site 1264, a continuous <inline-formula><mml:math id="M31" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 316 m shipboard
stratigraphic splice was developed back to the early Oligocene using
magnetic susceptibility and 600/450 nm colour reflectance data
(Shipboard Scientific Party Leg 208, 2004a).
Oligocene–early Miocene XRF ln(Ca <inline-formula><mml:math id="M32" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) data were used to verify the shipboard splice and produce a revised composite depth (rmcd) scale
(Liebrand et al., 2016, 2018). Liebrand
et al. (2016) filled four short Oligocene–early Miocene core gaps at Site 1264
with data from Site 1265 (Fig. 1; 28<inline-formula><mml:math id="M33" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>50.101<inline-formula><mml:math id="M34" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula> S, 2<inline-formula><mml:math id="M35" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>38.354<inline-formula><mml:math id="M36" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula> E, 3059 m water depth; Shipboard Scientific Party Leg 208, 2004b) to provide a continuous sedimentary sequence. Site 1264 and the relevant intervals of Site 1265 are characterised by high biogenic
carbonate, with shipboard analysis indicating an average CaCO<inline-formula><mml:math id="M37" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content
of 92 %–96 % (Shipboard Scientific Party
Leg 208, 2004a, b). At Site 1264, shipboard linear sedimentation rates (LSR)
derived from bio-magnetostratigraphy were exceptionally low for the
early–middle Miocene (19–12 Ma; LSR <inline-formula><mml:math id="M38" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 3.9–5.4 m Myr<inline-formula><mml:math id="M39" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>, average of 4.7 m Myr<inline-formula><mml:math id="M40" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>).
Higher shipboard LSR occurred during the Oligocene–early Miocene (30–19 Ma; LSR <inline-formula><mml:math id="M41" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 5.3–9.3 m Myr<inline-formula><mml:math id="M42" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>, average of 7.1 m Myr<inline-formula><mml:math id="M43" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) and early Plio-Pleistocene (3–0 Ma;
LSR <inline-formula><mml:math id="M44" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 4.5–7.4 m Myr<inline-formula><mml:math id="M45" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>, average of 6.0 m Myr<inline-formula><mml:math id="M46" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>). The highest shipboard LSR
occurred in the late Miocene–early Pliocene (12–3 Ma), where LSR average
15.9 m Myr<inline-formula><mml:math id="M47" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> (7.7–30.5 m Myr<inline-formula><mml:math id="M48" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>). The shipboard LSR for the Oligocene–early
Miocene (30–17 Ma) and Plio-Pleistocene (5.3–0.0 Ma) were confirmed by
previous studies on Sites 1264 and 1265, which also support the shipboard
notion that these sites are excellent recorders of orbital-scale climate
dynamics
(Liebrand
et al., 2011, 2016, 2017, 2018; Bell et al., 2014, 2015).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F1" specific-use="star"><?xmltex \currentcnt{1}?><?xmltex \def\figurename{Figure}?><label>Figure 1</label><caption><p id="d1e691"><bold>(a)</bold> Site overview showing location of Sites 1264 and 1265 on the Angola Basin side of Walvis Ridge, as well as <bold>(b)</bold> the differences between core box photos and line scan images compiled with CODD.  Figure made with GeoMapApp (<uri>http://www.geomapapp.org</uri>, last access: 9 September 2021)/CC BY/CC BY  (Ryan et al., 2009).</p></caption>
          <?xmltex \igopts{width=441.017717pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/2091/2021/cp-17-2091-2021-f01.png"/>

        </fig>

</sec>
<sec id="Ch1.S2.SS2">
  <label>2.2</label><title>Core images</title>
      <p id="d1e716">To assist with splice verification, astronomical tuning and data
interpretation, we compiled composite core images for ODP Site 1264 from
both cropped line scan images and core table-top photos (JANUS – <uri>http://www-odp.tamu.edu/database/</uri>, last access: May 2020 for core table-top photos and November 2014 for line scan images) using Code for Ocean
Drilling Data (CODD 2.1 – <uri>http://www.codd-home.net</uri>, last access: May 2021​​​​​​​; Wilkens et al., 2017). After cropping
the original line scan images, core section images were compiled into
a single image for each core and scaled to depth using the
“Includes_Core_Image_Assembly” functions. The line scan images obtained during ODP Leg 208
“Walvis Ridge” are redder in colour than they appear in the core table-top
photos. This is likely an artefact of the line-scanning calibration, which
had only recently been introduced at the time (Fig. 1). The individual core
images were also compiled from lighting-corrected table-top core box photos
using the “Includes_Core_Table_Photos” functions. These table-top core box images more realistically
represent the original colour of the cores. However, because the
core-box-derived images are exceptionally white, we preferentially use the
line-scan-derived images, as the sedimentary cyclicity at Site 1264 is
better visible in these images, and thus these are more beneficial to evaluating
and revising the stratigraphic splice together with XRF and physical
property data (see Fig. 2; Sect. 2.3 and 3.1). The individual
core box and line scan core images were then combined into a single composite
image along the revised Site 1264 splice using the “SpliceImages”
function. The individual core box and line scan core images from Site 1265
(Westerhold et al., 2017) were
spliced into the four Oligocene–early Miocene core gaps in the Site 1264 splice image
using the Site 1264 to Site 1265 ties from
Liebrand et al. (2016) updated to accommodate any splice revisions (see also Sect. 3.1 and Fig. S5 and Table S5 in the Supplement). This resulted in a continuous
spliced image of the sedimentary succession at Site 1264–1265 spanning the
early Oligocene to present day.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F2" specific-use="star"><?xmltex \currentcnt{2}?><?xmltex \def\figurename{Figure}?><label>Figure 2</label><caption><p id="d1e727">Overview of main splice change between the shipboard splice <bold>(a)</bold> and the revised splice presented in this study <bold>(b)</bold>. The interval between arrows on the splice was revised based on the ln(Ca <inline-formula><mml:math id="M49" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) data. The shipboard magnetic susceptibility (MS) is too low amplitude in the late Miocene in particular to robustly revise the splice, whereas ln(Ca <inline-formula><mml:math id="M50" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) data showed the sedimentary variability well. In certain high CaCO<inline-formula><mml:math id="M51" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> intervals Ba counts were also used to revise the composite splice (Fig. S3). The individual holes are shown for the shipboard splice only, with splice intervals shown between consecutive turquoise (top) and purple (bottom)
vertical lines.</p></caption>
          <?xmltex \igopts{width=497.923228pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/2091/2021/cp-17-2091-2021-f02.png"/>

        </fig>

</sec>
<sec id="Ch1.S2.SS3">
  <label>2.3</label><title>X-ray fluorescence core scanning</title>
      <p id="d1e773">XRF core scanner data were collected at ODP Site 1264 between 0 and 205 rmcd
(revised metres composite depth, this study) to connect with previously published XRF
core-scanning data spanning 205–315.96 rmcd (Liebrand
et al., 2016). The new XRF data were generated in four measurement campaigns
in 2011 (195–205 rmcd), 2013 (29.21–153.28 rmcd), 2017 (141.49–195.12 rmcd)
and 2018 (0–33.35 rmcd). Ca, Fe, K, Mn, Si and Ti were measured directly at
the core surface of Site 1264 archive halves using a 10 kV run at 1–2 cm
resolution over a 1.2 cm<inline-formula><mml:math id="M52" display="inline"><mml:msup><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:math></inline-formula> area with a slit size of 10 mm down-core and
12 mm cross-core with XRF Core Scanner II/III (AVAATECH serial no. 2/12) at
the MARUM – University of Bremen. In 2018, Ba and Sr were additionally
measured with the same slit conditions using a 50 kV run across intervals
that proved more problematic to accurately correlate between holes. The
following settings were used: in 2011, 10 kV/0.15 mA/10 s count time/Cl-Rh filter on the MARUM XRF III (see also Liebrand
et al., 2016); in 2013, 10 kV/0.2 mA/15 s count time/Cl-Rh
filter on the MARUM XRF III; in 2017, 10 kV/0.15 mA/15 s count time/no filter on the MARUM XRF II; and in 2018, 50 kV/0.5 mA/7 s count time/Cu filter and 10 kV/0.035 mA/7 s count time/no filter on the MARUM XRF III. The split core surface was covered with a 4 <inline-formula><mml:math id="M53" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>m
thick SPEXCerti Prep Ultralene1 foil to avoid contamination of the XRF
measurement unit and desiccation of the sediment. Selected intervals were
rerun during successive campaigns to account for differences in measurement
intensity between datasets, including with the published Liebrand
et al. (2016) data. All data were inspected directly following collection,
and outliers were removed if they were clearly associated with cracks and/or
uneven sediment surface. A further four measurement points, often at section
ends, were removed because intensities were<?pagebreak page2094?> unrealistically low. The XRF datasets
collected in 2011, 2013 and 2017 were calibrated to the 2018 dataset using an individual
linear regression for each element (see Supplement and Figs. S1 and S2). The 2011 XRF dataset includes the data originally published in Liebrand et al. (2016). All XRF core-scanning
intensity data and derived information are reported in Table S1.</p>
</sec>
<sec id="Ch1.S2.SS4">
  <label>2.4</label><?xmltex \opttitle{XRF-derived CaCO${}_{{3}}$ estimates and CaCO${}_{{3}}$ MARs}?><title>XRF-derived CaCO<inline-formula><mml:math id="M54" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> estimates and CaCO<inline-formula><mml:math id="M55" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs</title>
      <p id="d1e820">Liebrand et al. (2016) showed that the XRF ln(Ca <inline-formula><mml:math id="M56" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) ratio shows a strong positive
correlation with shipboard coulometric CaCO<inline-formula><mml:math id="M57" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data from Site 1264
(Shipboard Scientific Party Leg 208, 2004a). We use a
similar approach to generate a continuous record of CaCO<inline-formula><mml:math id="M58" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content using
the combined Site 1264 XRF ln(Ca <inline-formula><mml:math id="M59" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) dataset calibrated to the shipboard CaCO<inline-formula><mml:math id="M60" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data (%CaCO<inline-formula><mml:math id="M61" display="inline"><mml:mrow><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub><mml:mo>=</mml:mo><mml:mn mathvariant="normal">80.238</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">1.069</mml:mn><mml:mo>+</mml:mo><mml:mo>(</mml:mo><mml:mn mathvariant="normal">2.526</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.188</mml:mn><mml:mo>×</mml:mo><mml:mi>ln⁡</mml:mi><mml:mo>(</mml:mo><mml:mrow class="chem"><mml:mi mathvariant="normal">Ca</mml:mi></mml:mrow><mml:mo>/</mml:mo><mml:mrow class="chem"><mml:mi mathvariant="normal">Fe</mml:mi></mml:mrow><mml:mo>)</mml:mo><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>; <inline-formula><mml:math id="M62" display="inline"><mml:mrow><mml:msup><mml:mi>r</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M63" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.622; Fig. S6). The
Oligocene–early Miocene calibration used by Liebrand
et al. (2016) is within the 2<inline-formula><mml:math id="M64" display="inline"><mml:mi mathvariant="italic">σ</mml:mi></mml:math></inline-formula> uncertainty of the new %CaCO<inline-formula><mml:math id="M65" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
calibration, which equates to <inline-formula><mml:math id="M66" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>2.2 % in the calibrated
%CaCO<inline-formula><mml:math id="M67" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> dataset. The uncertainty in the calibration likely originates
from the scatter of the shipboard coulometry-derived %CaCO<inline-formula><mml:math id="M68" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data
that were used in the calibration. This uncertainty only pertains to the
absolute %CaCO<inline-formula><mml:math id="M69" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> values. The trends and cyclicity observed in the
calibrated CaCO<inline-formula><mml:math id="M70" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data are independent of this uncertainty, as these
patterns are present in the raw ln(Ca <inline-formula><mml:math id="M71" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) time series.</p>
      <p id="d1e997">The new and recalibrated %CaCO<inline-formula><mml:math id="M72" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data from Site 1264 were combined
with the %CaCO<inline-formula><mml:math id="M73" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data from Site 1265 (Liebrand
et al., 2016) to form a <inline-formula><mml:math id="M74" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 315 m/<inline-formula><mml:math id="M75" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 30 Myr
continuous record of CaCO<inline-formula><mml:math id="M76" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content at Walvis Ridge. Bulk and CaCO<inline-formula><mml:math id="M77" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
mass accumulation rates (MARs; g cm<inline-formula><mml:math id="M78" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M79" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) were calculated using the
following formulas:

                <disp-formula specific-use="gather" content-type="numbered"><mml:math id="M80" display="block"><mml:mtable displaystyle="true"><mml:mlabeledtr id="Ch1.E1"><mml:mtd><mml:mtext>1</mml:mtext></mml:mtd><mml:mtd><mml:mrow><mml:mstyle class="stylechange" displaystyle="true"/><mml:msub><mml:mi mathvariant="normal">MAR</mml:mi><mml:mi mathvariant="normal">Bulk</mml:mi></mml:msub><mml:mo>=</mml:mo><mml:msub><mml:mi mathvariant="italic">ρ</mml:mi><mml:mi mathvariant="normal">dry</mml:mi></mml:msub><mml:mo>×</mml:mo><mml:mi mathvariant="normal">LSR</mml:mi><mml:mo>,</mml:mo></mml:mrow></mml:mtd></mml:mlabeledtr><mml:mlabeledtr id="Ch1.E2"><mml:mtd><mml:mtext>2</mml:mtext></mml:mtd><mml:mtd><mml:mrow><mml:mstyle displaystyle="true" class="stylechange"/><mml:msub><mml:mi mathvariant="normal">MAR</mml:mi><mml:mrow><mml:msub><mml:mrow class="chem"><mml:mi mathvariant="normal">CaCO</mml:mi></mml:mrow><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:msub><mml:mo>=</mml:mo><mml:msub><mml:mi mathvariant="italic">ρ</mml:mi><mml:mi mathvariant="normal">dry</mml:mi></mml:msub><mml:mo>×</mml:mo><mml:mi mathvariant="normal">LSR</mml:mi><mml:mo>×</mml:mo><mml:mfenced open="(" close=")"><mml:mstyle displaystyle="true"><mml:mfrac style="display"><mml:mrow><mml:mi mathvariant="italic">%</mml:mi><mml:msub><mml:mrow class="chem"><mml:mi mathvariant="normal">CaCO</mml:mi></mml:mrow><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow><mml:mn mathvariant="normal">100</mml:mn></mml:mfrac></mml:mstyle></mml:mfenced><mml:mo>,</mml:mo></mml:mrow></mml:mtd></mml:mlabeledtr><mml:mlabeledtr id="Ch1.E3"><mml:mtd><mml:mtext>3</mml:mtext></mml:mtd><mml:mtd><mml:mrow><mml:mstyle displaystyle="true" class="stylechange"/><mml:msub><mml:mi mathvariant="normal">MAR</mml:mi><mml:mi mathvariant="normal">detrital</mml:mi></mml:msub><mml:mo>=</mml:mo><mml:msub><mml:mi mathvariant="normal">MAR</mml:mi><mml:mi mathvariant="normal">Bulk</mml:mi></mml:msub><mml:mo>-</mml:mo><mml:msub><mml:mi mathvariant="normal">MAR</mml:mi><mml:mrow><mml:msub><mml:mrow class="chem"><mml:mi mathvariant="normal">CaCO</mml:mi></mml:mrow><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:msub><mml:mo>.</mml:mo></mml:mrow></mml:mtd></mml:mlabeledtr></mml:mtable></mml:math></disp-formula>

            The LSR (here in cm kyr<inline-formula><mml:math id="M81" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) were calculated using the new astrochronology (Sect. 4).
Dry bulk density <inline-formula><mml:math id="M82" display="inline"><mml:mrow><mml:msub><mml:mi mathvariant="italic">ρ</mml:mi><mml:mi mathvariant="normal">dry</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula> (g cm<inline-formula><mml:math id="M83" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) was estimated using the
shipboard gamma ray attenuation (GRA) bulk density data calibrated to the
shipboard discrete dry density data (Shipboard Scientific
Party Leg 208, 2004a) (Fig. S7). The uncertainty in the MARs
is difficult to quantify. The largest uncertainties affecting bulk,
CaCO<inline-formula><mml:math id="M84" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> and detrital MARs arise from uncertainties in the <inline-formula><mml:math id="M85" display="inline"><mml:mrow><mml:msub><mml:mi mathvariant="italic">ρ</mml:mi><mml:mi mathvariant="normal">dry</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula>, which was calculated using shipboard GRA and discrete dry density
data, and the LSR, both of which are difficult to estimate. CaCO<inline-formula><mml:math id="M86" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs
additionally have <inline-formula><mml:math id="M87" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>2.2 % 2<inline-formula><mml:math id="M88" display="inline"><mml:mi mathvariant="italic">σ</mml:mi></mml:math></inline-formula> calibration uncertainty.
However, as %CaCO<inline-formula><mml:math id="M89" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> is so high at Site 1264, the %CaCO<inline-formula><mml:math id="M90" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
calibration uncertainty will have a smaller affect<?pagebreak page2095?> compared with the changes
in LSR. Because detrital MARs are low and calculated using the difference
between bulk and CaCO<inline-formula><mml:math id="M91" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs, changes in detrital MARs should be treated
cautiously.</p>
</sec>
</sec>
<sec id="Ch1.S3">
  <label>3</label><title>Results</title>
<sec id="Ch1.S3.SS1">
  <label>3.1</label><title>Site 1264 splice revision, off-splice mapping, and the Site 1264 to Site 1265 correlation</title>
      <p id="d1e1308">The line scan core photos and XRF data, especially the ln(Ca <inline-formula><mml:math id="M92" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) and Ba
data, show that there are several misalignments in sedimentary features when
using the shipboard composite depth scale, leading to duplicated and/or
missing intervals in the shipboard splice (Fig. 2). These<?pagebreak page2096?> misalignments are
especially pronounced in intervals where the shipboard physical property
data was low amplitude due to very high CaCO<inline-formula><mml:math id="M93" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content, e.g. during the
late Miocene–early Pliocene interval. Predominantly using the XRF ln(Ca <inline-formula><mml:math id="M94" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe)
ratio, the shipboard splice was verified between 0 and 205 rmcd and revised
where needed (Figs. 2 and S3; Tables S2 and S3). Where the inter-hole correlation based on the ln(Ca <inline-formula><mml:math id="M95" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) ratio was
ambiguous, the Ba data were used (see Fig. S3). Revisions
were made between 27 and 149 rmcd and generally resulted in changes of less
than 0.6 m relative to the shipboard composite depth (Tables S2
and S3), with the exception where Core 1264A-11H was shifted by <inline-formula><mml:math id="M96" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>1.26 m
relative to Core 1264B-11H to improve the correlation (Fig. 2). The core
images, the new ln(Ca <inline-formula><mml:math id="M97" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) data, and shipboard 600/450 nm colour reflectance and MS data (Shipboard Scientific Party Leg 208, 2004a)
were also used to map off-splice intervals of Holes 1264A and 1264B onto the
splice between 0 and 196.13 rmcd (Table S4).</p>
      <p id="d1e1356">Liebrand
et al. (2016, 2018) previously revised the Oligocene–early Miocene interval of
the composite depth scale, stratigraphic splice and mapping pairs for Site 1264, as well as the Site-to-Site correlation between Sites 1264 and 1265.
The revisions in the upper sedimentary succession (0–205 rmcd) result in a
cumulative shift of <inline-formula><mml:math id="M98" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>1.96 m to the Liebrand
et al. (2016, 2018) Site 1264 composite depth scale, stratigraphic splice,
mapping pairs and Site 1264 depths in the Site 1264 to Site 1265 correlation
between 196.13 and 315.96 rmcd (Tables S2–S5). Furthermore,
the line scan composite core photos showed that the mapping of Core
1264B-29H to the splice, erroneously corrected in Liebrand et al. (2018) from original mapping in Liebrand
et al. (2016), should be adjusted (see Fig. S4 and Table S4).
The composite depth scale and splice revisions resulted in two small gaps in
the Plio-Pleistocene Site 1264 isotope record (Bell et al.,
2014): <inline-formula><mml:math id="M99" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 15 cm (<inline-formula><mml:math id="M100" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 17 kyr) between 27.25–27.40 rmcd and <inline-formula><mml:math id="M101" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 25 cm (<inline-formula><mml:math id="M102" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 11 kyr) between 54.18–54.43 rmcd, which were filled with new isotope data
(Westerhold et al., 2020).</p>
</sec>
<sec id="Ch1.S3.SS2">
  <label>3.2</label><?xmltex \opttitle{Site~1264 XRF intensities, CaCO${}_{{3}}$ estimates and MARs}?><title>Site 1264 XRF intensities, CaCO<inline-formula><mml:math id="M103" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> estimates and MARs</title>
      <p id="d1e1412">The XRF-derived CaCO<inline-formula><mml:math id="M104" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content at Site 1264 is generally high
throughout, ranging between minimum values of 92 % and maximum values of
97 % (Fig. 3). The range of observed %CaCO<inline-formula><mml:math id="M105" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> variability is close to
the 2.2 % uncertainty associated with the calibration. However, we are
confident that both the long-term trends and short-term variability
discussed below represent true changes in carbonate content, as these
patterns originate in the original ln(Ca <inline-formula><mml:math id="M106" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) ratio. The calibration
uncertainty is most relevant to the absolute carbonate content. The
recalibrated CaCO<inline-formula><mml:math id="M107" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content span 93 %–96 % between <inline-formula><mml:math id="M108" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 205
and <inline-formula><mml:math id="M109" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 316 rmcd (early Oligocene–early Miocene), which agrees
within error with the original calibrated CaCO<inline-formula><mml:math id="M110" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content reported and
discussed in detail by Liebrand
et al. (2016). The lowest CaCO<inline-formula><mml:math id="M111" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content (92 %–93 %) occurs between 205
and 190 rmcd (middle Miocene). The CaCO<inline-formula><mml:math id="M112" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content shows especially clear
0.5 m cycles in this interval. CaCO<inline-formula><mml:math id="M113" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content increases slightly to
94 % between 190 and 180 rmcd (middle Miocene) and then remains around
94 %–95 % until <inline-formula><mml:math id="M114" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 118 rmcd (early late Miocene). The
CaCO<inline-formula><mml:math id="M115" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content initially displays short 0.6 m cycles, but after
<inline-formula><mml:math id="M116" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 185 rmcd (middle Miocene), 0.2–0.3 m cycles are superimposed
upon <inline-formula><mml:math id="M117" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1–2 m cycles. CaCO<inline-formula><mml:math id="M118" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content then undergoes a
two-step rapid increase to 96 % between <inline-formula><mml:math id="M119" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 118 and 110 rmcd
and again to 97 % between 105 and 100 rmcd (both latest Miocene).
CaCO<inline-formula><mml:math id="M120" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content remains around 97 % until 90 rmcd, after which the
CaCO<inline-formula><mml:math id="M121" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content decreases slightly to around 96 % until 40 rmcd (early
Pliocene). Between <inline-formula><mml:math id="M122" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 118 and <inline-formula><mml:math id="M123" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 40 rmcd (latest
Miocene–early Pliocene), <inline-formula><mml:math id="M124" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1.0 m cycles and occasionally
<inline-formula><mml:math id="M125" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 0.5 m cycles are prevalent, although the amplitude of the
short-term cycles is reduced compared to the deeper interval. CaCO<inline-formula><mml:math id="M126" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
content slowly drops to 95 % by 15 rmcd (Pleistocene) and decrease further to 93 %–94 % in the upper 15 m of the record. Short-term cycles are less
well expressed in this upper interval. The Si and K intensities are
comparable throughout the record, although Si is generally slightly higher
than K (Fig. 3). Both elements, together with Fe and Ti intensities, display
the same short-term variability and long-term trends (Figs. 3 and
S2), indicating that these elements reflect changes in
aluminosilicates. As the trends of Si and K are inverse to those seen in the
CaCO<inline-formula><mml:math id="M127" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content, this supports that Site 1264 is predominantly composed
of carbonate and clay, with minimal influence of biogenic silica. The
amplitude of changes in Si and K becomes much smaller relative to CaCO<inline-formula><mml:math id="M128" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
content changes between <inline-formula><mml:math id="M129" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 115 and 0 rmcd compared to between
<inline-formula><mml:math id="M130" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 315 and 115 rmcd.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F3" specific-use="star"><?xmltex \currentcnt{3}?><?xmltex \def\figurename{Figure}?><label>Figure 3</label><caption><p id="d1e1638">On the new revised composite depth (rmcd) <bold>(a)</bold> Site 1264 XRF Si (green) and K (teal) intensities, <bold>(b)</bold> %CaCO<inline-formula><mml:math id="M131" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data derived from ln(Ca <inline-formula><mml:math id="M132" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) for Sites 1264 (dark red) and 1265 (black), <bold>(c)</bold> bulk and CaCO<inline-formula><mml:math id="M133" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs for Sites 1264 (bulk is dark blue; CaCO<inline-formula><mml:math id="M134" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> is light blue) and 1265 (bulk is black; CaCO<inline-formula><mml:math id="M135" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> is dark grey), <bold>(d)</bold> sedimentation rates in m Myr<inline-formula><mml:math id="M136" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> for Sites 1264 (light grey) and 1265 (black), and the
combined composite core photo for Site 1264–1265 compiled using line
scan <bold>(e)</bold> and core box photo images <bold>(f)</bold>. The depth-domain wavelet spectra are shown for the %CaCO<inline-formula><mml:math id="M137" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data after it was detrended to remove all cycles greater than 2 m <bold>(g)</bold> or greater than 40 m <bold>(h)</bold>. The periods are highlighted in metres. The wavelets were generated using the code from Torrence and Compo (1998) and Grinsted et al. (2004). The approximate stratigraphic location of the MCO and the LMBB are highlighted by shaded grey areas.</p></caption>
          <?xmltex \igopts{width=455.244094pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/2091/2021/cp-17-2091-2021-f03.png"/>

        </fig>

      <p id="d1e1737">Because CaCO<inline-formula><mml:math id="M138" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content accounts for <inline-formula><mml:math id="M139" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 90 % of the sediment
mass, the bulk (0.3–4.7 g cm<inline-formula><mml:math id="M140" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M141" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) and CaCO<inline-formula><mml:math id="M142" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> (0.3–4.5 g cm<inline-formula><mml:math id="M143" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M144" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) MARs are remarkably similar, with trends controlled almost
completely by variability in LSR (Fig. 3). LSR also strongly affect detrital
MARs; however, these remain low throughout at Site 1264 (0.01–0.2 g cm<inline-formula><mml:math id="M145" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M146" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>). The Oligocene-early Miocene CaCO<inline-formula><mml:math id="M147" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs generally oscillate between 1 and 2 g cm<inline-formula><mml:math id="M148" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M149" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> from <inline-formula><mml:math id="M150" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 315 to 205 rmcd.
MARs are very low (<inline-formula><mml:math id="M151" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 0.3–0.7 g cm<inline-formula><mml:math id="M152" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M153" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) between 205 and 190 rmcd, before slowly increasing to 1.0–2.5 g cm<inline-formula><mml:math id="M154" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M155" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> between 190 and <inline-formula><mml:math id="M156" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 118 rmcd. The highest CaCO<inline-formula><mml:math id="M157" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs (2.5–4.5 g cm<inline-formula><mml:math id="M158" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M159" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) occur between <inline-formula><mml:math id="M160" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 118 and 35 rmcd, with values
decreasing back to 1–2 g cm<inline-formula><mml:math id="M161" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M162" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> after <inline-formula><mml:math id="M163" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 35 rmcd. The
highest frequency variability in the bulk and CaCO<inline-formula><mml:math id="M164" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs results from
changes in dry bulk density (Shipboard Scientific Party
Leg 208, 2004a); however, this variability is smaller than that variability
reflecting the changing resolution of the astrochronology (see Sect. 4.2).</p>
</sec>
</sec>
<?pagebreak page2097?><sec id="Ch1.S4">
  <label>4</label><title>Depth and age models for Site 1264</title>
<sec id="Ch1.S4.SS1">
  <label>4.1</label><title>Cyclostratigraphy and initial bio-/magnetostratigraphic age model</title>
      <p id="d1e2039">Here, we describe the imprint of cyclic patterns on the Site 1264 CaCO<inline-formula><mml:math id="M165" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
content (Fig. 3). New cyclostratigraphy covers the upper <inline-formula><mml:math id="M166" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 205 m of the sedimentary succession at Site 1264, which corresponds to strata of
middle Miocene to late Pleistocene age. Cyclostratigraphy of the lowermost
<inline-formula><mml:math id="M167" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 111 m from Site 1264 (between <inline-formula><mml:math id="M168" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 205 and
<inline-formula><mml:math id="M169" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 316 rmcd), which corresponds to the early Oligocene to early
Miocene time interval, was previously described in great detail
(Liebrand
et al., 2016). A cycle interpretation and age model were also previously
presented for the upper <inline-formula><mml:math id="M170" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 57 m from Site 1264
(Bell et al., 2014); however, due to several splice
revisions between 27 and 55 rmcd (see Sect. 3.1) we briefly re-evaluate
the cycle imprint on this part of the record (see Sect. 4.1.3 and 4.1.4).</p>
      <p id="d1e2087">The upper <inline-formula><mml:math id="M171" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 205 m is split into four intervals that are
characterised by distinct cyclic patterns and/or average sedimentation rates
(Sect. 4.1.1, 4.1.2, 4.1.3 and 4.1.4). We apply an 11th order
polynomial age model computed on selected (i.e. high-quality) biostratigraphic and
magnetostratigraphic depth-age points to obtain a first-order approximation
of the durations of the cycles that we identify in the depth domain (see
Table S6, Figs. S8 and S9). After applying the
polynomial age model, the record was tuned to generate an astrochronology
(Sect. 4.2; Figs. 4 and S10).</p>

      <?xmltex \floatpos{p}?><fig id="Ch1.F4" specific-use="star"><?xmltex \currentcnt{4}?><?xmltex \def\figurename{Figure}?><label>Figure 4</label><caption><p id="d1e2099">Overview of the new astrochronology for the last 30 Myr. The four
panels show the different tuning strategies employed. (I.a) 30–9.7 Ma:
CaCO<inline-formula><mml:math id="M172" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>(/benthic <inline-formula><mml:math id="M173" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O) to eccentricity; (I.b) 9.7–8.0 Ma:
CaCO<inline-formula><mml:math id="M174" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> to <inline-formula><mml:math id="M175" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mo>(</mml:mo><mml:mi>T</mml:mi><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>; (II) 8.0–3.3 Ma: CaCO<inline-formula><mml:math id="M176" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>(/benthic <inline-formula><mml:math id="M177" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O)
to <inline-formula><mml:math id="M178" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mi>T</mml:mi></mml:mrow></mml:math></inline-formula>–<inline-formula><mml:math id="M179" display="inline"><mml:mi>P</mml:mi></mml:math></inline-formula>; and (III) 3.3–0.0 Ma: benthic <inline-formula><mml:math id="M180" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O to LR04. The
composite core photo compiled from line scan images is used here as it
highlights the sedimentological cyclicity best. Zoomed in figures showing
the exact depth-age tie points are shown in Fig. S10.</p></caption>
          <?xmltex \igopts{width=611.734252pt, angle=90}?><graphic xlink:href="https://cp.copernicus.org/articles/17/2091/2021/cp-17-2091-2021-f04.png"/>

        </fig>

<sec id="Ch1.S4.SS1.SSS1">
  <label>4.1.1</label><?xmltex \opttitle{Depth interval between 205 and 190\,rmcd}?><title>Depth interval between 205 and 190 rmcd</title>
      <?pagebreak page2099?><p id="d1e2209">The depth-domain wavelet analysis of the CaCO<inline-formula><mml:math id="M181" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content between 205 and
190 rmcd highlights the lithological cycles in %CaCO<inline-formula><mml:math id="M182" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>, which broadly
varies around 2 and 0.5 m in length (Fig. 3) The biostratigraphic and magnetostratigraphic (bio-magnetostratigraphic)
age model indicates that the LSR vary around 5 m Myr<inline-formula><mml:math id="M183" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>. Applying this LSR to
the 2 and 0.5 m cycles yield durations of approximately 405 and
<inline-formula><mml:math id="M184" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr, respectively. These durations are in very close
agreement with the strong eccentricity pacing of CaCO<inline-formula><mml:math id="M185" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content
variability found for the underlying early Oligocene–early Miocene sediment
package (Liebrand
et al., 2016). We infer that eccentricity pacing of the carbonate record
remained dominant from the base of Site 1264 to <inline-formula><mml:math id="M186" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 190 rmcd
regardless of the changes in LSR, which were lower between 205 and 190 rmcd
compared to the deeper interval (Fig. 3). This interpretation is in agreement
with visual inspection of the data, which shows bundling of <inline-formula><mml:math id="M187" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr cycles (e.g. the <inline-formula><mml:math id="M188" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 95 and <inline-formula><mml:math id="M189" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 125 kyr
cycles) within longer 405 kyr cycles (Figs. 3 and 4I.a).</p>
</sec>
<sec id="Ch1.S4.SS1.SSS2">
  <label>4.1.2</label><?xmltex \opttitle{Depth interval between 190 and 115\,rmcd}?><title>Depth interval between 190 and 115 rmcd</title>
      <p id="d1e2296">The depth interval between 190 and 115 rmcd is marked by cycles that
gradually shift from 0.2 to 0.3 m, from <inline-formula><mml:math id="M190" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1 to
<inline-formula><mml:math id="M191" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 2 m, and from <inline-formula><mml:math id="M192" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 4 to <inline-formula><mml:math id="M193" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 6 m respectively in
the depth-domain wavelet analysis of the CaCO<inline-formula><mml:math id="M194" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data (Fig. 3). The
bio-magnetostratigraphic age model indicates that these gradually shifting,
quasi-stable cyclicities in the depth domain reflect low but gradually
increasing LSR from <inline-formula><mml:math id="M195" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 10 m Myr<inline-formula><mml:math id="M196" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> between 190 and 160 rmcd to
<inline-formula><mml:math id="M197" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 15 m Myr<inline-formula><mml:math id="M198" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> between 160 and 115 rmcd. Based on this initial age
model, we tentatively link the 0.2 to 0.3 m cycles to precession, the
<inline-formula><mml:math id="M199" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1 to <inline-formula><mml:math id="M200" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 2 m cycles to <inline-formula><mml:math id="M201" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr
eccentricity and the <inline-formula><mml:math id="M202" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 4 to <inline-formula><mml:math id="M203" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 6 m cycles to 405 kyr eccentricity (Fig. S9). These inferred durations of these
cycles correspond to known ratios between precession, short and long
eccentricity of five precession cycles per <inline-formula><mml:math id="M204" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr cycle,
and about four <inline-formula><mml:math id="M205" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr cycles per 405 kyr cycle. Overall,
the bio-magnetostratigraphic age model suggests that the <inline-formula><mml:math id="M206" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity cycle remains the most strongly expressed cycle between
17 and 13 Ma, in line with the strong <inline-formula><mml:math id="M207" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity
cycles observed between 30 and 17 Ma (see Sect. 4.1.1 and Liebrand
et al., 2016). Strong <inline-formula><mml:math id="M208" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity cycles were also
noted in this interval in the equatorial Pacific
(Kochhann et al., 2016).
The presence of a weak 405 kyr signal in the Site 1264 CaCO<inline-formula><mml:math id="M209" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content
contrasts with the Oligocene interval, for which no uniform imprint of the
405 kyr cycle on CaCO<inline-formula><mml:math id="M210" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content could be discerned (Liebrand
et al., 2016).</p>
</sec>
<sec id="Ch1.S4.SS1.SSS3">
  <label>4.1.3</label><?xmltex \opttitle{Depth interval between 115 and 35\,rmcd}?><title>Depth interval between 115 and 35 rmcd</title>
      <p id="d1e2474">Because of several splice revisions in the upper 55 rmcd of Site 1264 (see
Sect. 3.1.), we deem a modest re-evaluation of the cyclostratigraphy for
this interval beneficial for subsequently obtaining a final tuned age model
(see also Sect. 4.1.4.), even though detailed investigations were
previously made (Bell et al., 2014). Visible inspection of
the CaCO<inline-formula><mml:math id="M211" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content data and the associated depth-domain wavelet analysis
both show that there is short-term cyclicity present in the data between 115
and 35 rmcd (Fig. 3). However, the amplitude of these cycles is much reduced
in comparison to the previous depth intervals, which means that the cycles
are not statistically significant above the 95 % level in the depth-domain
wavelet analyses. Nevertheless, we document depth periodicities of
<inline-formula><mml:math id="M212" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 0.5, <inline-formula><mml:math id="M213" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1, <inline-formula><mml:math id="M214" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 3–4, and
<inline-formula><mml:math id="M215" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 10–12 m. We compute average LSR of 20 to 30 m Myr<inline-formula><mml:math id="M216" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> based on
the bio-magnetostratigraphic ages and tentatively infer that these depth
cycles are respectively linked to the 20 kyr precession (<inline-formula><mml:math id="M217" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 0.5 m), the 40 kyr obliquity (<inline-formula><mml:math id="M218" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 1 m), and the <inline-formula><mml:math id="M219" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110
and 405 kyr eccentricity cycles (<inline-formula><mml:math id="M220" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 3–4 and <inline-formula><mml:math id="M221" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 10–12 m) (Figs. 3, S8 and S9). Between 55 and 35 rmcd, we
visually derive an antiphase relationship between CaCO<inline-formula><mml:math id="M222" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content data
and benthic foraminiferal <inline-formula><mml:math id="M223" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O data (Fig. S11), which aids our tuning approach for this interval (see Sect. 4.2.2).</p>
</sec>
<sec id="Ch1.S4.SS1.SSS4">
  <label>4.1.4</label><?xmltex \opttitle{Depth interval between 35 and 0\,rmcd}?><title>Depth interval between 35 and 0 rmcd</title>
      <p id="d1e2592">At Site 1264, clear cyclicity is generally hard to observe in the upper
interval of the depth-domain CaCO<inline-formula><mml:math id="M224" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content wavelet analysis, except for
the presence of occasional stronger <inline-formula><mml:math id="M225" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1.0–1.5 m cycles.
Visually, we can identify higher-frequency cycles in the CaCO<inline-formula><mml:math id="M226" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content
data; however, the amplitude of these cycles is muted compared to the cycles
observed between 115 and 35 rmcd. Benthic foraminiferal <inline-formula><mml:math id="M227" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O
maxima (Bell et al., 2014) appear to coincide with
CaCO<inline-formula><mml:math id="M228" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima in the upper 35 m; however, this phase relationship
is not well defined throughout this interval and becomes less clear at the
top of the record. We derive averaged LSR of <inline-formula><mml:math id="M229" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 10 m Myr<inline-formula><mml:math id="M230" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> for 0–35 rmcd based on the initial bio-magnetostratigraphic age model. The observed
1.0 to 1.5 m cycles are probably linked to the <inline-formula><mml:math id="M231" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr
eccentricity paced cycles or the main ice age cycles of the middle and late
Pleistocene. This would indicate a change in response of both benthic
foraminiferal <inline-formula><mml:math id="M232" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O and CaCO<inline-formula><mml:math id="M233" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content during this time
interval, in line with the evolution of the global cryosphere and climate
systems during this time
(Bailey
et al., 2013). Based on the initial age model we note an absence of clear
precession and obliquity-paced cyclicity in both benthic foraminiferal
<inline-formula><mml:math id="M234" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O and CaCO<inline-formula><mml:math id="M235" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content records during the last 2.5 Ma
(Fig. S9).</p>
</sec>
</sec>
<sec id="Ch1.S4.SS2">
  <label>4.2</label><title>Astronomically tuned age model</title>
      <p id="d1e2717">Two published astrochronologies exist for Site 1264–1265: (1) an Oligocene–early
Miocene one (30 to 17 Ma), based on tuning CaCO<inline-formula><mml:math id="M236" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content to eccentricity
(Liebrand et al., 2016), and (2) a Plio-Pleistocene one (5.3 to 0 Ma) based on a correlation of the Site 1264 benthic foraminiferal <inline-formula><mml:math id="M237" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O
record to the LR04 Plio-Pleistocene benthic <inline-formula><mml:math id="M238" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O stack
(Lisiecki and Raymo, 2005; Bell et al., 2014). Because of
the splice revisions between 27 and 149 rmcd at Site 1264, we re-evaluated
the Bell et al. (2014) chronology in the early Pliocene
prior to 3.5 Ma/<inline-formula><mml:math id="M239" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 27 rmcd. The Oligocene to early Miocene
astrochronology remains unchanged, but we updated the depth–age tie points
to accommodate the cumulative <inline-formula><mml:math id="M240" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>1.96 m shift in the revised composite depth
scale of the overlying sedimentary sequence. The cyclostratigraphic analyses
in the depth-domain indicate that the combined Site 1264–1265 CaCO<inline-formula><mml:math id="M241" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
content record is suitable for developing an astrochronology for the
interval 17–3.5 Ma (see Sect. 4.1) using the flexible best-practice
guidelines outlined in Sinnesael
et al. (2019). Because of the variable imprint of eccentricity (<inline-formula><mml:math id="M242" display="inline"><mml:mi>E</mml:mi></mml:math></inline-formula>),
obliquity (<inline-formula><mml:math id="M243" display="inline"><mml:mi>T</mml:mi></mml:math></inline-formula>) and precession (<inline-formula><mml:math id="M244" display="inline"><mml:mi>P</mml:mi></mml:math></inline-formula>) recorded at Site 1264, it was not possible
to implement a uniform tuning strategy for the entire record. In all, we
employed three distinct strategies to achieve a 30 Myr astrochronology for
Site 1264 (Table S7 and Fig. S10):
<list list-type="custom"><list-item><label>I.</label>
      <p id="d1e2798">30–8.0 Ma: CaCO<inline-formula><mml:math id="M245" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content tuned to eccentricity; obliquity is also used in 2.4 Myr minima (when stable in the solution).
<list list-type="custom"><list-item><label>a.</label>
      <p id="d1e2812">30–9.7 Ma: CaCO<inline-formula><mml:math id="M246" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content tuned to <inline-formula><mml:math id="M247" display="inline"><mml:mi>E</mml:mi></mml:math></inline-formula> (visually aided by <inline-formula><mml:math id="M248" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O, where available).</p></list-item><list-item><label>b.</label>
      <p id="d1e2843">9.7–8.0 Ma: CaCO<inline-formula><mml:math id="M249" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> tuned content to <inline-formula><mml:math id="M250" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mo>(</mml:mo><mml:mi>T</mml:mi><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>.</p></list-item></list></p></list-item><list-item><label>II.</label>
      <p id="d1e2870">8.0–3.3 Ma: CaCO<inline-formula><mml:math id="M251" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content tuned to <inline-formula><mml:math id="M252" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mi>T</mml:mi><mml:mo>-</mml:mo><mml:mi>P</mml:mi></mml:mrow></mml:math></inline-formula> (visually aided by <inline-formula><mml:math id="M253" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O, where available).</p></list-item><list-item><label>III.</label>
      <p id="d1e2908">3.3–0.0 Ma: benthic <inline-formula><mml:math id="M254" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O tuned to LR04.</p></list-item></list></p>
<?pagebreak page2100?><sec id="Ch1.S4.SS2.SSS1">
  <label>4.2.1</label><?xmltex \opttitle{Early Oligocene--late Miocene (30.0--8.0\,Ma)}?><title>Early Oligocene–late Miocene (30.0–8.0 Ma)</title>
      <p id="d1e2930">Liebrand
et al. (2016) showed that CaCO<inline-formula><mml:math id="M255" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content maxima between 30 and 17 Ma  coincide with benthic
<inline-formula><mml:math id="M256" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O maxima, which are both antiphase with the <inline-formula><mml:math id="M257" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity components. They generated an astrochronology by tuning
CaCO<inline-formula><mml:math id="M258" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima to eccentricity maxima (see Liebrand
et al., 2016, for details). As the variability and dominant cyclicity in
CaCO<inline-formula><mml:math id="M259" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content for the 17–8 Ma interval are comparable to the 30–17 Ma
interval (see Sect. 4.3.1 and 4.3.2), we consider the inverse phase
relationship between CaCO<inline-formula><mml:math id="M260" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content and <inline-formula><mml:math id="M261" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr
eccentricity to be valid between 30 and 8 Ma. We therefore also employ the
Liebrand
et al. (2016) tuning strategy of CaCO<inline-formula><mml:math id="M262" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima to eccentricity
maxima between 17 and 8 Ma (Fig. 4). When benthic foraminiferal stable isotope
records become available for the interval between 17 and 8 Ma, the stability of
the Oligocene–late Miocene phase relationship between CaCO<inline-formula><mml:math id="M263" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content and
<inline-formula><mml:math id="M264" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity can be tested.</p>
      <p id="d1e3020">The CaCO<inline-formula><mml:math id="M265" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content to eccentricity tuning strategy is very robust where
the amplitude modulation of <inline-formula><mml:math id="M266" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity is high;
however, this amplitude is muted during 2.4 Myr eccentricity minima
(<inline-formula><mml:math id="M267" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 17.0–16.6, <inline-formula><mml:math id="M268" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 14.6–14.2, <inline-formula><mml:math id="M269" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 12.6–12.2, <inline-formula><mml:math id="M270" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 9.7–9.3 Ma). The imprint of obliquity is
apparent in these 2.4 Myr eccentricity minima and can act as an alternative
tuning target when <inline-formula><mml:math id="M271" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity amplitude is
reduced. However, because of uncertainties in past changes to tidal
dissipation and dynamical ellipticity, the exact phase of obliquity is not
known before 10 Ma
(Lourens
et al., 2005; Zeeden et al., 2013, 2014). We therefore apply two slightly
adapted approaches of the Liebrand
et al. (2016) tuning strategy to the 17–8 Ma interval.
<list list-type="custom"><list-item><label>I.a.</label>
      <p id="d1e3077">From 17 to 9.7 Ma, we tune CaCO<inline-formula><mml:math id="M272" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima to <inline-formula><mml:math id="M273" display="inline"><mml:mi>E</mml:mi></mml:math></inline-formula> maxima (La2004;
Laskar et al.,
2004), with an uncertainty better than <inline-formula><mml:math id="M274" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>50 kyr. This uncertainty
increases to up to <inline-formula><mml:math id="M275" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>100 kyr in the 2.4 Myr minima at <inline-formula><mml:math id="M276" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 17.0–16.6, <inline-formula><mml:math id="M277" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 14.6–14.2 and <inline-formula><mml:math id="M278" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 12.6–12.2 Ma
(Fig. 4I.a).</p></list-item><list-item><label>I.b.</label>
      <p id="d1e3133">From 9.7 to 8.0 Ma, we tune CaCO<inline-formula><mml:math id="M279" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima to <inline-formula><mml:math id="M280" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mo>(</mml:mo><mml:mi>T</mml:mi><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula> maxima (La2004;
Laskar et al.,
2004). Generally, the CaCO<inline-formula><mml:math id="M281" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima are tuned to <inline-formula><mml:math id="M282" display="inline"><mml:mi>E</mml:mi></mml:math></inline-formula> maxima, with
an uncertainty better than <inline-formula><mml:math id="M283" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>50 kyr. During the 2.4 Myr eccentricity
minima <inline-formula><mml:math id="M284" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 9.7–9.3 Ma, CaCO<inline-formula><mml:math id="M285" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima are tuned to ET
maxima (uncertainty up to <inline-formula><mml:math id="M286" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>40 kyr; Fig. 4I.b).</p></list-item></list>
We chose to tune to the La2004 solution (Laskar et al., 2004), as over the last 30 Myr the eccentricity components are essentially identical to the La2011_ecc3L solution (Laskar et al., 2011) used in Liebrand
et al. (2016). Furthermore, the obliquity solution used in the (I.b) approach is
currently only available in the La2004 solution.</p>
      <p id="d1e3207">There was potential to develop an astrochronology at precession level, as
the cyclostratigraphic analyses show that precession cycles are also
imprinted in the CaCO<inline-formula><mml:math id="M287" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content younger than 14 Ma (see Sect. 4.1).
However, as uncertainties in past tidal dissipation and dynamical
ellipticity mean the phase of precession is also uncertain before 10 Ma
(Lourens et al., 2005; Zeeden et al.,
2013), we chose a conservative strategy of only tuning to eccentricity prior
to 9.7 Ma.</p>
</sec>
<sec id="Ch1.S4.SS2.SSS2">
  <label>4.2.2</label><?xmltex \opttitle{Late Miocene--mid-Pliocene (8.0--3.3\,Ma)}?><title>Late Miocene–mid-Pliocene (8.0–3.3 Ma)</title>
      <?pagebreak page2101?><p id="d1e3228">After 8 Ma, the <inline-formula><mml:math id="M288" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity imprint on CaCO<inline-formula><mml:math id="M289" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
content decreases significantly, whilst the imprint of obliquity and
precession is more prevalent between 8 and 2.5 Ma. We therefore apply a
different tuning strategy between 8.0 and 3.3 Ma to accommodate the change
in prevalent cyclicity in the CaCO<inline-formula><mml:math id="M290" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content from
eccentricity–precession-driven content (older than 8 Ma) to
obliquity–precession-driven content (younger than 8 Ma) (see Sect. 4.1). The
contrasting relationship between benthic <inline-formula><mml:math id="M291" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O and CaCO<inline-formula><mml:math id="M292" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
content in the latest Miocene–Pleistocene compared to the Oligocene–early
Miocene also indicates that different tuning approaches are warranted. Where latest Miocene–Pleistocene benthic <inline-formula><mml:math id="M293" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O and
CaCO<inline-formula><mml:math id="M294" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content are both available (6.0–3.3 Ma; Bell et al., 2014; Westerhold et
al., 2020), the two proxies show an inverse relationship, with the
obliquity- and precession-driven CaCO<inline-formula><mml:math id="M295" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima coinciding with
benthic <inline-formula><mml:math id="M296" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O maxima. This contrast to the Oligocene–early
Miocene relationship between these proxies with the 110 kyr
eccentricity-driven CaCO<inline-formula><mml:math id="M297" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content minima coinciding with benthic
<inline-formula><mml:math id="M298" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O minima (Liebrand
et al., 2016). The late Miocene–Pleistocene phase relationship between
benthic <inline-formula><mml:math id="M299" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O and obliquity is well established, with benthic
<inline-formula><mml:math id="M300" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O minima coinciding with obliquity maxima (Shackleton
et al., 1995; Shackleton and Hall, 1997; Hodell et al., 2001; Zeeden et al.,
2013; Drury et al., 2017, 2018b). As the relationship between benthic
<inline-formula><mml:math id="M301" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O and CaCO<inline-formula><mml:math id="M302" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content is inverse after 6.0 Ma, we assume
that CaCO<inline-formula><mml:math id="M303" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content maxima correlate to obliquity maxima for the entire
8 to 3.3 Ma interval. Precession and obliquity are the two prevalent
cyclicities present in both the CaCO<inline-formula><mml:math id="M304" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content and benthic <inline-formula><mml:math id="M305" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O data. The interference pattern observed in both benthic <inline-formula><mml:math id="M306" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O and CaCO<inline-formula><mml:math id="M307" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content is most similar to an <inline-formula><mml:math id="M308" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mi>T</mml:mi><mml:mo>-</mml:mo><mml:mi>P</mml:mi></mml:mrow></mml:math></inline-formula> solution. We
therefore generated an astrochronology by tuning CaCO<inline-formula><mml:math id="M309" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> maxima to <inline-formula><mml:math id="M310" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mi>T</mml:mi><mml:mo>-</mml:mo><mml:mi>P</mml:mi></mml:mrow></mml:math></inline-formula>
maxima guided by benthic <inline-formula><mml:math id="M311" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O where these are available
(uncertainty up to <inline-formula><mml:math id="M312" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>10 kyr; Fig. 4II). Based on the shipboard
biostratigraphy, there was some indication that there might be an
unconformity of <inline-formula><mml:math id="M313" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 0.6 Myr in the late Miocene at the base of
Core 1264A-7H (<inline-formula><mml:math id="M314" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 76–77 rmcd) (Shipboard
Scientific Party Leg 208, 2004a). However, we find excellent agreement
between the CaCO<inline-formula><mml:math id="M315" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content and the <inline-formula><mml:math id="M316" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mi>T</mml:mi><mml:mo>-</mml:mo><mml:mi>P</mml:mi></mml:mrow></mml:math></inline-formula> solution, with 80 and 75 rmcd
correlating well with 6.3–6.1 Ma (Fig. 4II).</p>
</sec>
<sec id="Ch1.S4.SS2.SSS3">
  <label>4.2.3</label><?xmltex \opttitle{Mid-Pliocene--Pleistocene (3.3--0.0\,Ma)}?><title>Mid-Pliocene–Pleistocene (3.3–0.0 Ma)</title>
      <p id="d1e3532">We used the original Bell et al. (2014) age model between
3.3 and 0 Ma because no changes were made to the shipboard splice in the
upper 27 rmcd (3.5 Myr). The Bell et al. (2014) age model
was generated by correlating a benthic foraminiferal <inline-formula><mml:math id="M317" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O stack
comprising data from ODP Sites 1264 and 1267 to the LR04 <inline-formula><mml:math id="M318" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O
stack (Lisiecki and Raymo, 2005). We validated the
Bell et al. (2014) age model by comparing the Site 1264
<inline-formula><mml:math id="M319" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O record to the equatorial Atlantic CR17 <inline-formula><mml:math id="M320" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O
stack (Wilkens et al., 2017), which has
an independent tuning based on MS and lightness. The agreement between the
1264 and CR <inline-formula><mml:math id="M321" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O records is very good (Fig. 4III), which
further supports the accuracy of the original Bell et al. (2014) age model in this interval.</p>
</sec>
</sec>
</sec>
<sec id="Ch1.S5">
  <label>5</label><title>Discussion</title>
<sec id="Ch1.S5.SS1">
  <label>5.1</label><?xmltex \opttitle{History of South Atlantic CaCO${}_{{3}}$ deposition and its changing orbital pacing since the Oligocene}?><title>History of South Atlantic CaCO<inline-formula><mml:math id="M322" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition and its changing orbital pacing since the Oligocene</title>
      <p id="d1e3618">Previous work at ODP Site 1264 shows that the recovered sediments record the
orbital climate variability of the Southeast Atlantic for the last 30 Myr
(Shipboard
Scientific Party Leg 208, 2004a; Bell et al., 2014, 2015; Liebrand et al.,
2016). Oligocene to early Miocene carbonate and benthic <inline-formula><mml:math id="M323" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O
records from Site 1264 show that the early Coolhouse was dominated by large
<inline-formula><mml:math id="M324" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity-driven variability in the Antarctic ice
sheet (for
full discussion, see Liebrand et al., 2016, 2017). By the Pliocene, Atlantic
benthic <inline-formula><mml:math id="M325" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">13</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>C gradients indicate that North Atlantic Deep Water
(NADW) heavily influenced Southeast Atlantic Site 1264
(for full discussion,
see Bell et al., 2014, 2015). The new complete and continuous depth
(<inline-formula><mml:math id="M326" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 316 m; Sect. 3.1; Fig. 3) and age (<inline-formula><mml:math id="M327" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 30 Myr;
Sect. 4; Fig. 4) model presented here constitutes a reference framework for
future palaeoclimatic and palaeoceanographic studies at Site 1264.
Furthermore, the new data (Fig. 5) enable investigation of how long-term
climate trends and orbital-scale climate variability impacted this region,
especially between 17 and 5 Ma, for which no high-resolution Southeast
Atlantic records previously existed.</p>

      <?xmltex \floatpos{p}?><fig id="Ch1.F5" specific-use="star"><?xmltex \currentcnt{5}?><?xmltex \def\figurename{Figure}?><label>Figure 5</label><caption><p id="d1e3666">New data from Site 1264–1265 on the new astrochronology. <bold>(a)</bold> Site 1264 benthic foraminiferal <inline-formula><mml:math id="M328" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O (Bell
et al., 2014; Liebrand et al., 2016; Westerhold et al., 2020) and the benthic <inline-formula><mml:math id="M329" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O Megasplice (De Vleeschouwer et al., 2017). <bold>(b)</bold> Site 1264 Si intensity (counts). The left axis of <bold>(c)</bold> shows %<inline-formula><mml:math id="M330" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 63 <inline-formula><mml:math id="M331" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>m coarse fraction (%CF) (Liebrand et al., 2016; Keating-Bitonti and Peters, 2019), and the
right axis shows XRF-derived CaCO<inline-formula><mml:math id="M332" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data from Sites 1264 (dark red) and 1265
(black). <bold>(d)</bold> Bulk and CaCO<inline-formula><mml:math id="M333" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs for Sites 1264 (dark and light blue, respectively) and 1265 (black and grey, respectively). <bold>(e)</bold> Eccentricity and <bold>(f)</bold> obliquity solutions (Laskar et al., 2004). <bold>(g)</bold> Line scan and <bold>(h)</bold> core box photo Site 1264–1265 composite core photos. <bold>(i)</bold> Wavelet spectra in the time domain of the CaCO<inline-formula><mml:math id="M334" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data detrended to remove cycles over 200 kyr. <bold>(j)</bold> Wavelet spectra in the time domain of the CaCO<inline-formula><mml:math id="M335" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data detrended to remove cycles over 4 Myr (Torrence and Compo, 1998; Grinsted et al., 2004). The MCO, mMCT and LMBB are annotated.</p></caption>
          <?xmltex \igopts{width=569.055118pt, angle=90}?><graphic xlink:href="https://cp.copernicus.org/articles/17/2091/2021/cp-17-2091-2021-f05.png"/>

        </fig>

      <p id="d1e3781">At Site 1264, CaCO<inline-formula><mml:math id="M336" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content is very high, with all long- and short-term
variability occurring between 92 % and 97.5 % CaCO<inline-formula><mml:math id="M337" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> (Fig. 5). CaCO<inline-formula><mml:math id="M338" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content varied between 94 % and 96 % during the Oligocene-early Miocene (30–18.5 Ma), with MARs of <inline-formula><mml:math id="M339" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1–2.5 g cm<inline-formula><mml:math id="M340" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M341" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> and are discussed in greater detail in Liebrand et al. (2016). The lowest CaCO<inline-formula><mml:math id="M342" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content (92 %–93.5 %) and MARs (<inline-formula><mml:math id="M343" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 0.3–0.7 g cm<inline-formula><mml:math id="M344" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M345" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) occur between <inline-formula><mml:math id="M346" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 18.5 and 14.4 Ma, which broadly coincides with the Miocene Climatic Optimum (MCO; 17–14.7 Ma; Shevenell et al.,
2004; Holbourn et al., 2005) (see Sect. 5.2 for discussion). Broadly
concurrent with cooling in the lead up to the middle Miocene Climate Transition
(mMCT; <inline-formula><mml:math id="M347" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 13.9 Ma), CaCO<inline-formula><mml:math id="M348" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content increases and remains
between 94 % and 96 % during the early late Miocene (14.4–8.0 Ma), coincident with MARs of <inline-formula><mml:math id="M349" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1–2.5 g cm<inline-formula><mml:math id="M350" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M351" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> (see Sect. 5.2 for discussion). The highest CaCO<inline-formula><mml:math id="M352" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content (96 %–97.5 %) and MARs (2.5–4.5 g cm<inline-formula><mml:math id="M353" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M354" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) occur between 8 and 4 Ma (Fig. 5), potentially indicating high
carbonate productivity coincident with the known age of the global late
Miocene–early Pliocene Biogenic Bloom (LMBB; acronym from
Lyle et al., 2019) (see Sect. 5.3 for
further discussion).</p>
      <?pagebreak page2103?><p id="d1e3973">Carbonate deposition is strongly affected by the balance between biogenic
carbonate productivity (mostly in the surface water) and carbonate
dissolution in the water column and at the sea floor. Sedimentary processes,
such as dilution with terrigenous material and/or the removal of
fine-grained material through winnowing, can affect both the amount and
composition of the carbonate preserved. The relative importance of biogenic
productivity versus dissolution is discussed in detail in Liebrand
et al. (2016) for the Oligocene to early Miocene, in Sect. 5.2 for the
early–middle Miocene and in Sect. 5.3 for the late Miocene–early Pliocene.
Over the last 30 Myr, detrital MARs were low, indicating that dilution with
terrigenous material was not a major contributing factor in controlling
carbonate deposition at Site 1264. Winnowing may have removed fine fraction
material, including coccolith carbonate, thereby reducing carbonate
deposition at Site 1264. By comparing MARs between nearby sites recovered
during DSDP Leg 74, Shackleton et
al. (1984) suggested that winnowing may have affected parts of the Walvis
Ridge. They suggested that winnowing was especially pronounced at DSDP Site 526 (1054 m water depth) since the late Oligocene. Site 1264 is situated on
a very gentle slope above the lysocline and carbonate compensation depth
(palaeowater depths: 2–2.5 km). Winnowing likely had less of an effect on Site 1264 compared to Site 526, as Site 1264 is not positioned on the shallowest parts of the Walvis Ridge bathymetry. Nonetheless,
Shackleton et al. (1984) also found
some indication of winnowing at DSDP Site 525 (2467 m water depth) since the
late Pliocene. Independent constraints on winnowing are not available for
the entire 30 Myr interval; however, detailed fine fraction weights are
available between 30 and 17 Ma (Liebrand
et al., 2016; their Fig. 2). If these data are interpreted as a proxy for
winnowing, this would suggest that winnowing is modest during the middle
Oligocene, increasing during late Oligocene warming and relatively high
across the Oligocene–Miocene Transition (OMT; Fig. 5). During the early Miocene
(post OMT, pre-middle Miocene) winnowing is comparable to late Oligocene values
(Fig. 5). There is evidence for winnowing to have increased towards the
condensed middle Miocene part of the Site 1264 record, as there is an
increase in both high-resolution and low-resolution percent <inline-formula><mml:math id="M355" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 63 <inline-formula><mml:math id="M356" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>m coarse fraction (%CF) (Liebrand
et al., 2016; Keating-Bitonti and Peters, 2019) (Fig. 5). However, between
18.5 and 8 Ma, the Site 1264 %CF varies within a 5 % range, suggesting the amount of winnowing remained stable (Fig. 5; Keating-Bitonti and Peters, 2019). After <inline-formula><mml:math id="M357" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 3 Ma, %CF gradually increases from 20 % to 40 % (Fig. 5), which is the largest increase seen in the entire record and could indicate
that Site 1264 is affected by winnowing at this time. The presence of
winnowing is also supported by the fact that deeper Walvis Ridge Site 1266
and Site 1267 both have higher sedimentation rates than Site 1264 in the last 3 Ma, whereas the opposite would be expected if deep-sea dissolution alone was considered (productivity should affect all sites similarly).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F6" specific-use="star"><?xmltex \currentcnt{6}?><?xmltex \def\figurename{Figure}?><label>Figure 6</label><caption><p id="d1e4000">Zoomed-in panels highlighting the three distinctly different
orbital controls on Southeast Atlantic CaCO<inline-formula><mml:math id="M358" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition. <bold>(a)</bold> Example of strong eccentricity (<inline-formula><mml:math id="M359" display="inline"><mml:mi>E</mml:mi></mml:math></inline-formula>) pacing present between 30 and 13 Ma. <bold>(b)</bold> Example of the prevalent eccentricity-modulated precession pacing present between 14 and 8 Ma. <bold>(c)</bold> Example of the pervasive obliquity forcing present between 8 and <inline-formula><mml:math id="M360" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 3.3 Ma. An example of stronger obliquity appearing in a 2.4 Myr eccentricity minimum, when eccentricity-modulated precession is muted, is also shown in <bold>(b)</bold>. CaCO<inline-formula><mml:math id="M361" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> minima correlate with eccentricity maxima between 30 and 8 Ma <bold>(a, b)</bold>. Between 8 and 0 Ma, CaCO<inline-formula><mml:math id="M362" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> maxima
correlate with obliquity maxima <bold>(c)</bold>.</p></caption>
          <?xmltex \igopts{width=341.433071pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/2091/2021/cp-17-2091-2021-f06.png"/>

        </fig>

      <p id="d1e4069">The influence of the long 405 kyr eccentricity on CaCO<inline-formula><mml:math id="M363" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition at
Site 1264 is complicated. The imprint of the 405 kyr cycle on CaCO<inline-formula><mml:math id="M364" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
content was not constant during the Oligocene interval at Site 1264
(Liebrand
et al., 2016). This contrasts with the clearer imprint of a 405 kyr cycle on
CaCO<inline-formula><mml:math id="M365" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition during the Miocene between <inline-formula><mml:math id="M366" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 21 and 5 Ma.
For periodicities shorter than 405 kyr, we can recognise three distinctly
different orbital imprints on the variability in CaCO<inline-formula><mml:math id="M367" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content (Figs. 5 and 6).
<list list-type="order"><list-item>
      <p id="d1e4118">The <inline-formula><mml:math id="M368" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity is the dominant driver between 30 and
<inline-formula><mml:math id="M369" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 13 Ma (Fig. 6a).</p></list-item><list-item>
      <p id="d1e4136">Precession-driven %CaCO<inline-formula><mml:math id="M370" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> oscillations appear <inline-formula><mml:math id="M371" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 14–13 Ma and are the main pacer of short-term variability until <inline-formula><mml:math id="M372" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 8 Ma (Fig. 6b).</p></list-item><list-item>
      <p id="d1e4163">Obliquity becomes a significant driver at Site 1264 after <inline-formula><mml:math id="M373" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.7 Ma and together with precession imprints a characteristic interference pattern on %CaCO<inline-formula><mml:math id="M374" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> (Fig. 6c).</p></list-item></list>
Although different tuning strategies are used to generate a continuous
astrochronology (Sect. 4.2), these shifts in imprinted cyclicity are also
visible in the depth and bio-magnetostratigraphic age model spectra,
indicating that the shifts are independent of the changes in tuning strategy
(see Sect. 4.1 and Fig. S9).</p>
      <p id="d1e4183">The three pacings observed in Southeast Atlantic CaCO<inline-formula><mml:math id="M375" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition
broadly coincide with major developments in climate, the cryosphere and/or
the carbon cycle over the last 30 Myr. At Site 1264, the strong expression
of <inline-formula><mml:math id="M376" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity-driven %CaCO<inline-formula><mml:math id="M377" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> variability
between 17 and 13 Ma parallels the dominant pacing of %CaCO<inline-formula><mml:math id="M378" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> during the
Oligocene–early Miocene (30–17 Ma; Figs. 5 and 6a; for further details, see
Liebrand et al., 2016). The prevalence of <inline-formula><mml:math id="M379" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity pacing
at Site 1264 is in line with the wider understanding that Oligocene to middle Miocene unipolar Coolhouse climate was predominantly paced by short-term
eccentricity during widespread global warmth (Pälike
et al., 2006; Tian et al., 2013; Holbourn et al., 2014, 2015; Beddow et al.,
2016, 2018; Voigt et al., 2016; Kochhann et al., 2016; Liebrand et al.,
2016, 2017; De Vleeschouwer et al., 2017, 2020; Westerhold et al., 2020).
The strong <inline-formula><mml:math id="M380" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr cyclicity observed in marine archives is
attributed to eccentricity-driven changes in ice volume and/or deep-sea
temperature, likely associated with changes in atmospheric CO<inline-formula><mml:math id="M381" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula> (Pälike
et al., 2006; Holbourn et al., 2015; Liebrand et al., 2017; Greenop et al.,
2019).</p>
      <p id="d1e4244">The orbital imprint on CaCO<inline-formula><mml:math id="M382" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content shifts between 14 and 13 Ma, when
eccentricity-modulated precession cycles progressively become more clearly
superimposed on the larger <inline-formula><mml:math id="M383" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr cycles. These precession
cycles remain the main driver of carbonate deposition until <inline-formula><mml:math id="M384" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 8 Ma, although obliquity cycles are visible during the 2.4 Myr eccentricity
minima from <inline-formula><mml:math id="M385" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 12.6 to 12.2 Ma and <inline-formula><mml:math id="M386" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 9.7 to 9.3 Ma, when the imprint of precession and <inline-formula><mml:math id="M387" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity
is muted (Figs. 5 and 6b). Strong obliquity was also observed in benthic
<inline-formula><mml:math id="M388" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O data from the South China Sea during the <inline-formula><mml:math id="M389" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 9.7–9.3 Ma node (Holbourn
et al., 2013). The strong obliquity intervals that are observed across
multiple marine archives support the idea that obliquity exerts greater control on
the climate system as a whole when the orbital configuration is
characterised by long-term eccentricity minima coincident with long-term
obliquity maxima (Holbourn
et al., 2013, 2018; Drury et al., 2017; Levy et al., 2019). The shift to
stronger precession pacing occurs after global cooling and the reglaciation
of Antarctica across the mMCT (<inline-formula><mml:math id="M390" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 13.9 Ma; Holbourn et al., 2005).
Some precession-driven %CaCO<inline-formula><mml:math id="M391" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> cycles were observed and superimposed on
larger <inline-formula><mml:math id="M392" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity cycles between 23.5 and 19.5 Ma at
Site 1264 (Fig. 5; Liebrand
et al., 2016). However, the relative amplitude of eccentricity and
precession is different in the middle to late Miocene compared to the
Oligocene–early Miocene. In the Oligocene–early Miocene, the amplitude of
the <inline-formula><mml:math id="M393" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity cycles in CaCO<inline-formula><mml:math id="M394" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content were
greater than the precession-driven CaCO<inline-formula><mml:math id="M395" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content cycles. In contrast,
we observe a decrease in strength of the <inline-formula><mml:math id="M396" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr
eccentricity cycles concurrent with the strong precession pacing of the
CaCO<inline-formula><mml:math id="M397" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content between 14 and 8 Ma (Fig. 5). The influence of early–middle Miocene climate<?pagebreak page2104?> evolution on Southeast Atlantic carbonate deposition is
discussed further in Sect. 5.2.</p>
      <p id="d1e4376">Although some power remains in the <inline-formula><mml:math id="M398" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity
bandwidth, the orbital imprint seen in CaCO<inline-formula><mml:math id="M399" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content changes around 7.7 Ma to a strong obliquity–precession interference pattern, which remains
visible until <inline-formula><mml:math id="M400" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 3.3 Ma (Figs. 5 and 6c). The onset of prevalent
obliquity–precession pacing of %CaCO<inline-formula><mml:math id="M401" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> observed at Site 1264 after
<inline-formula><mml:math id="M402" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.7 Ma has been observed globally in benthic <inline-formula><mml:math id="M403" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O records and is associated with increased influence of
high-latitude processes, such as enhanced glacial activity and high-latitude
cooling (Drury
et al., 2016, 2017, 2018b; Holbourn et al., 2018; see also Sect. 5.3).
Although benthic <inline-formula><mml:math id="M404" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O data are not available at Site 1264
between 8.0 and 6.0 Ma, the obliquity–precession interference pattern is visible
in the benthic <inline-formula><mml:math id="M405" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O record between 6.0 and 3.3 Ma (Fig. 4).
Relative to the Oligocene–early late Miocene, the amplitude of the
variability in CaCO<inline-formula><mml:math id="M406" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content is reduced during the latest Miocene and
early Pliocene. Concurrent with the waning influence of <inline-formula><mml:math id="M407" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity at Site 1264, the highest CaCO<inline-formula><mml:math id="M408" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content (96 %–97.5 %)
of the entire record occurs between 8 and<?pagebreak page2105?> 4 Ma. The influence of the complex
late Miocene climate system on carbonate deposition is discussed in Sect. 5.3.</p>
      <p id="d1e4477">After 3.3 Ma, the short-term orbital imprint is more difficult to
characterise. The wavelet analysis shows that <inline-formula><mml:math id="M409" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr
eccentricity influence increases in the Plio-Pleistocene compared to the
latest Miocene (Fig. 5). The influence of some obliquity and precession
forcing on %CaCO<inline-formula><mml:math id="M410" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> remains until <inline-formula><mml:math id="M411" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 0.9 Ma, when the
<inline-formula><mml:math id="M412" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity pacing characteristic of the middle
Pleistocene appears after the mid-Pleistocene Transition (MPT;
Bell et al., 2014). Compared to Site 1264, the transition
from <inline-formula><mml:math id="M413" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 40 to <inline-formula><mml:math id="M414" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr pacing is recorded
more clearly at nearby Site 1267, where it is visible in the benthic <inline-formula><mml:math id="M415" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O data, composite core photos and physical property data
(physical
property data from Shipboard Scientific Party Leg 208, 2004c; benthic
<inline-formula><mml:math id="M416" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O data from Bell et al., 2014; composite core photos from
Westerhold et al., 2017). This difference in expression of the MPT may
partly relate to water depth differences between the sites, as the deeper
Site 1267 (4356 m water depth) may record a stronger deep-water signal
compared to Site 1264 (2507 m water depth). Alternatively, winnowing may
have obscured some of the cyclicity at Site 1264, considering the indication
that both Sites 1264 and 525 (both <inline-formula><mml:math id="M417" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 2.4–2.5 km water depth)
were affected by winnowing in the late Pliocene–early Pleistocene.
Nonetheless, although the onset of the Pleistocene <inline-formula><mml:math id="M418" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr
cycles is not exceptionally clear at Site 1264, it is apparent that these
cycles only appear after 0.9 Ma at both Sites 1264 and 1267 (Fig. 5), which
is considerably later than in the eastern equatorial Pacific, where
<inline-formula><mml:math id="M419" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr cycles first appear in carbonate records at 1.6 Ma
(Lyle et al., 2019).</p>
      <p id="d1e4568">Benthic foraminiferal <inline-formula><mml:math id="M420" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O records are only available for the
Oligocene–early Miocene (30–17 Ma; Liebrand et al., 2011, 2016) and the Plio-Pleistocene (5.3–0.0 Ma; Bell et al., 2014). It is therefore not yet possible to
track the evolution of the relationship between the climate–cryosphere
system (encompassed by benthic <inline-formula><mml:math id="M421" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O) and South Atlantic
carbonate deposition over the last 30 Myr. However, in contrast to the
in-phase %CaCO<inline-formula><mml:math id="M422" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>–benthic <inline-formula><mml:math id="M423" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O relationship on
<inline-formula><mml:math id="M424" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity periodicities between 30 and 17 Ma
(Liebrand
et al., 2016), the new Site 1264 %CaCO<inline-formula><mml:math id="M425" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data have an inverse
relationship with benthic <inline-formula><mml:math id="M426" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O on obliquity periodicities for
the last 6.0 Myr (Figs. 4 and S11). This points to a
considerably different relationship between the cryosphere and controls on
carbonate deposition at Site 1264 in the late Miocene–Pleistocene compared
to the Oligocene–early Miocene. The in-phase Oligocene to early Miocene
%CaCO<inline-formula><mml:math id="M427" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>-benthic <inline-formula><mml:math id="M428" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O relationship on <inline-formula><mml:math id="M429" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr periodicities observed at Site 1264 has been observed elsewhere for the
Oligocene through to the middle Miocene, including across the mMCT
(Holbourn
et al., 2014, 2015; Kochhann et al., 2016; Liebrand et al., 2016; Beddow et
al., 2018; Tian et al., 2018). It is possible that the
%CaCO<inline-formula><mml:math id="M430" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>–benthic <inline-formula><mml:math id="M431" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O relationship changed from in-phase
on 110 kyr eccentricity periodicities to anti-phase on obliquity
periodicities, concurrent with the <inline-formula><mml:math id="M432" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.7 Ma shift in
CaCO<inline-formula><mml:math id="M433" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition from a predominantly eccentricity–precession-paced
system to one that is more controlled by obliquity–precession. Such an
interpretation would further support the notion that the Earth's system
underwent a major shift in its response to orbital forcing in the late
Miocene–early Pliocene, with Northern Hemisphere high-latitude processes
steadily growing in importance in the latest Miocene
(Kirtland Turner, 2014; Drury et al., 2017, 2018b; De Vleeschouwer et al., 2020).</p>
</sec>
<sec id="Ch1.S5.SS2">
  <label>5.2</label><?xmltex \opttitle{Eccentricity to precession switch, low {\%}CaCO${}_{{3}}$ deposition and the early--middle Miocene warmth}?><title>Eccentricity to precession switch, low %CaCO<inline-formula><mml:math id="M434" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition and the early–middle Miocene warmth</title>
      <p id="d1e4723">The early–middle Miocene marks a warm interval where Antarctic ice volume
underwent major change and climatic trends deviated from the overall
Cenozoic cooling pattern (Miller
et al., 1991; Shevenell et al., 2004; Holbourn et al., 2005, 2014, 2015;
Tian et al., 2013, 2014; Super et al., 2018). The MCO
(defined in the benthic foraminiferal <inline-formula><mml:math id="M435" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O as between 17
and 14.7 Ma; Holbourn et al.,
2015) was characterised by pervasive global warmth and more humid
conditions, together with lower meridional temperature gradients and greatly
reduced continental ice sheets in Antarctica compared to the present day
(Lear
et al., 2000, 2015; Billups and Schrag, 2002; Shevenell et al., 2004; John
et al., 2011; Pound et al., 2012; Gasson et al., 2016; Levy et al., 2016).
Distal marine records that track variations in land ice volume and deep-sea
temperatures are marked by a strong <inline-formula><mml:math id="M436" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity
pacing, coupled with large 400 kyr driven carbon cycle perturbations
(Monterey Excursion) (Shevenell
et al., 2008; Holbourn et al., 2014, 2015; Tian et al., 2014; Kochhann et
al., 2016; Ohneiser and Wilson, 2018). The MCO warmth, ice volume decrease
and carbon cycle perturbations have been hypothesised to be driven by
increased atmospheric CO<inline-formula><mml:math id="M437" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula> levels associated with volcanic degassing
from the Columbia River Flood Basalts, with the earliest eruptions occurring
after <inline-formula><mml:math id="M438" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 17.2 Ma (Foster
et al., 2012; Barry et al., 2013; Greenop et al., 2014; Kasbohm and Schoene,
2018; Moore et al., 2018, 2020; Super et al., 2018; Cahoon et al., 2020;
Sosdian et al., 2020). The warm MCO conditions were reversed <inline-formula><mml:math id="M439" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 13.9 Ma during the mMCT when major continental ice sheets reappeared on
Antarctica associated with a large decrease in atmospheric CO<inline-formula><mml:math id="M440" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula> and
global temperatures (Shevenell
et al., 2004; Holbourn et al., 2005; Foster et al., 2012; Pound et al.,
2012; Badger et al., 2013; Lear et al., 2015; Gasson et al., 2016; Levy et
al., 2016; Super et al., 2018, 2020).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F7" specific-use="star"><?xmltex \currentcnt{7}?><?xmltex \def\figurename{Figure}?><label>Figure 7</label><caption><p id="d1e4779">Middle to late Miocene Site 1264–1265 data on the new astrochronology:
<bold>(a)</bold> BAYSPAR TEX<inline-formula><mml:math id="M441" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">86</mml:mn></mml:msub></mml:math></inline-formula> SSTs from Site 608 (blue dots are the 50th
percentile; medium blue is 65 % CL; light blue is 95 % CL;
Super et al., 2018); <bold>(b)</bold> benthic <inline-formula><mml:math id="M442" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O Megasplice (De Vleeschouwer et al., 2017); <bold>(c)</bold> XRF-derived CaCO<inline-formula><mml:math id="M443" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data from Site 1264–1265; <bold>(d)</bold> bulk and CaCO<inline-formula><mml:math id="M444" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs for Site 1264–1265 (dark and light blue, respectively); <bold>(e)</bold> Site 1264–1265 line scan and <bold>(f)</bold> core box composite core photos; and <bold>(g)</bold> wavelet spectra in
the time domain of the CaCO<inline-formula><mml:math id="M445" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data detrended to remove cycles <inline-formula><mml:math id="M446" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 200 kyr (Torrence and Compo, 1998; Grinsted et al., 2004). The approximate location of the MCO and the mMCT are also shown.</p></caption>
          <?xmltex \igopts{width=497.923228pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/2091/2021/cp-17-2091-2021-f07.png"/>

        </fig>

      <p id="d1e4865">Benthic foraminiferal <inline-formula><mml:math id="M447" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O records are not yet available at
Site 1264 for this interval, so it is not possible to recognise the MCO
using this dataset. Nonetheless, the lowest %CaCO<inline-formula><mml:math id="M448" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content
(92 %–93.5 %) and MARs (<inline-formula><mml:math id="M449" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 0.3–0.7 g cm<inline-formula><mml:math id="M450" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M451" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) occur
between <inline-formula><mml:math id="M452" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 18.5 and 14.4 Ma and broadly coincide with the MCO (Figs. 5c and 7c). Low detrital MARs (bulk–CaCO<inline-formula><mml:math id="M453" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs), Si and K intensity
indicates that biogenic silica and detrital input remains<?pagebreak page2106?> relatively
constant and minimal across this interval. The low detrital MARs at Site 1264 (average 0.09 g cm<inline-formula><mml:math id="M454" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M455" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) are comparable to the non-carbonate MARs of nearby sites drilled during Leg 74, particularly DSDP Site 525
(Shackleton et al., 1984). Dilution
was therefore not the main driving factor of the early–middle Miocene low
%CaCO<inline-formula><mml:math id="M456" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content at Site 1264. Winnowing could have removed the
<inline-formula><mml:math id="M457" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 63 <inline-formula><mml:math id="M458" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>m fraction at Site 1264 (Fig. 5); however, such winnowing
also tends to remove both small CaCO<inline-formula><mml:math id="M459" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> and detrital particles,
ultimately raising the overall CaCO<inline-formula><mml:math id="M460" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content but lowering the
CaCO<inline-formula><mml:math id="M461" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MAR (Marcantonio et al., 2014). A 10 % increase
in the percent <inline-formula><mml:math id="M462" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 63 <inline-formula><mml:math id="M463" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>m coarse fraction (%CF) after
<inline-formula><mml:math id="M464" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 18.5 Ma (Fig. 5; Liebrand
et al., 2016) indicates that some winnowing occurred. However, between 18.5 and 8 Ma, the Site 1264 %CF varies within a 5 % range but never increases to the high %CF values seen in the Plio-Pleistocene (Fig. 5;
Keating-Bitonti and Peters, 2019). This
indicates that increased dissolution and/or decreased productivity likely also
drove the early–middle Miocene low CaCO<inline-formula><mml:math id="M465" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content at Site 1264. An increase
of B <inline-formula><mml:math id="M466" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Ca concentration at Sites 1264 and 1266 after 15.5 Ma
(Kender et al., 2014) indicates that dissolution
influenced the early–middle Miocene low CaCO<inline-formula><mml:math id="M467" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content at Site 1264.</p>
      <p id="d1e5061">The recovery of %CaCO<inline-formula><mml:math id="M468" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content <inline-formula><mml:math id="M469" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 14.5 Ma agrees well
with the end of the MCO <inline-formula><mml:math id="M470" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 14.7 Ma (Holbourn et al., 2015). However,
at Site 1264, the decreasing CaCO<inline-formula><mml:math id="M471" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content starts <inline-formula><mml:math id="M472" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 18.5 Ma, which is <inline-formula><mml:math id="M473" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1.5 Myr before the decrease in benthic <inline-formula><mml:math id="M474" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O normally associated with the onset of the MCO (Fig. 5). During the
early–middle Miocene, low %CaCO<inline-formula><mml:math id="M475" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> and CaCO<inline-formula><mml:math id="M476" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs were
observed at multiple sites in the eastern equatorial Pacific Ocean (EEP;
DSDP Site 574; IODP Sites U1335 to U1338), initially decreasing after 18–17.5 Ma, before recovering to early Miocene values by 15–14.5 Ma
(Piela
et al., 2012; Kochhann et al., 2016). Multiproxy evidence at these EEP sites
indicates that the low %CaCO<inline-formula><mml:math id="M477" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> and CaCO<inline-formula><mml:math id="M478" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs values were
associated with increased deep-sea dissolution rather than decreased
productivity, with the peak dissolution occurring at the onset of the MCO
(Piela
et al., 2012;<?pagebreak page2107?> Kochhann et al., 2016). This dissolution horizon has been
traced regionally across the equatorial Pacific as the “Lavender” seismic
unconformity, with the dissolution potentially linked to the intensification
of proto-NADW formation leading to increased corrosive Antarctic Bottom
Water (AABW) reaching the Pacific
(Mayer et al., 1985). This hypothesis
could not be tested at the time due to the absence of any comparable
Atlantic carbonate records. However, the new evidence of low
%CaCO<inline-formula><mml:math id="M479" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> and CaCO<inline-formula><mml:math id="M480" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs at Site 1264 in the Southeast
Atlantic indicates that dissolution occurred in the Atlantic and the Pacific
during the early to middle Miocene. Increased dissolution across ocean basins
indicates a global forcing, supporting suggestions that the dissolution seen
in the Pacific was associated with elevated atmospheric <inline-formula><mml:math id="M481" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<inline-formula><mml:math id="M482" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula>, increased
carbon storage in the deep ocean and shoaling of the carbonate compensation
depth during the early–middle Miocene global warmth (Pälike
et al., 2012; Piela et al., 2012; Kochhann et al., 2016).</p>
      <p id="d1e5193">Assuming that the low CaCO<inline-formula><mml:math id="M483" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content and MARs at Site 1264 is
dissolution driven (e.g. see also Kender et al.,
2014), rather than reflecting a decrease in carbonate rain, there is
evidence that carbonate dissolution preceded the MCO by <inline-formula><mml:math id="M484" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1.5 Myr in the Southeast Atlantic (Site 1264) and <inline-formula><mml:math id="M485" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1.0–0.5 Myr
in the equatorial Pacific (Piela
et al., 2012; Kochhann et al., 2016). Few early–middle Miocene atmospheric
CO<inline-formula><mml:math id="M486" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula> or sea surface temperature (SST) records extend back to 18.5 Ma,
but long-term trends in early–middle Miocene TEX<inline-formula><mml:math id="M487" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">86</mml:mn></mml:msub></mml:math></inline-formula>-derived SSTs from the
North Atlantic Ocean indicate that SSTs may have been at MCO levels since
<inline-formula><mml:math id="M488" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 20 Ma (Super et al., 2018; Fig. 7a). It is
not yet clear whether elevated SSTs prior to the MCO are a global
phenomenon. However, the likely dissolution-induced lows in Southeast
Atlantic and equatorial Pacific CaCO<inline-formula><mml:math id="M489" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> deposition up to
<inline-formula><mml:math id="M490" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1.5 Myr before the MCO indicate that the MCO itself was
preconditioned by elevated temperatures and atmospheric <inline-formula><mml:math id="M491" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<inline-formula><mml:math id="M492" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula>.</p>
      <p id="d1e5277">Shortly after the MCO, the overall Cenozoic cooling trend resumes across the
mMCT with the reappearance of large ice sheets on Antarctica around 13.9 Ma.
At Site 1264, the %CaCO<inline-formula><mml:math id="M493" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> values increase after <inline-formula><mml:math id="M494" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 14.5 Ma, which could reflect decreased deep-sea dissolution and/or increased
surface ocean productivity. Between 14 and 13 Ma, the orbital imprint on
CaCO<inline-formula><mml:math id="M495" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> at Site 1264 progressively shifts from <inline-formula><mml:math id="M496" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr
eccentricity-dominated pacing to precession-dominated pacing superimposed on
the <inline-formula><mml:math id="M497" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity cycles (Figs. 6a, b and 7c). In
comparison to the Oligocene–early Miocene, the <inline-formula><mml:math id="M498" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr
eccentricity cycles are more muted, and the precession cycles are of higher
amplitude and more clearly expressed during the middle to late Miocene (Figs. 5 and
6b). The change in orbital imprint at Site 1264 after the mMCT may indicate
that productivity in this region became more sensitive to precession forcing
following changes to ocean circulation and/or the hydrological cycle driven
by the reglaciation of Antarctica, global cooling and increased meridional
temperature gradients. The shift towards strong precession pacing occurs as
carbonate content recovers after the MCO. Site 1264 likely experienced
increased carbonate deposition during the MCO as indicated by low LSR and
MARs between 18.5 and 14.4 Ma. The increased preservation of precession cycles
at Site 1264 after 14 Ma (i.e. after the mMCT) could also reflect a shift
in deep-water circulation patterns bringing less corrosive deep waters to
Site 1264, which is supported by the increase in B <inline-formula><mml:math id="M499" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Ca at Sites 1264 and 1266
(Kender et al., 2014). This deep-water change would
have enabled better preservation of precession-driven productivity cycles
after the mMCT compared to the early–middle Miocene.</p>
</sec>
<sec id="Ch1.S5.SS3">
  <label>5.3</label><title>Late Miocene-early Pliocene Biogenic Bloom</title>
      <p id="d1e5342">The latest Miocene (<inline-formula><mml:math id="M500" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 8–5.3 Ma) was a complicated and dynamic
interval when climate and ecosystems recognisable to the present-day first
appeared (Herbert et al., 2016). There is abundant
evidence for a global and long-lasting increase in primary productivity in
the global surface ocean during the late Miocene to early Pliocene
(Farrell
et al., 1995; Dickens and Owen, 1999; Diester-Haass et al., 2002, 2005).
This late Miocene–early Pliocene Biogenic Bloom (LMBB; as defined by
Lyle et al., 2019) has been recognised
between <inline-formula><mml:math id="M501" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 8 and 4 Ma in upwelling and oligotrophic areas of
all major oceanic basins (Kroon
et al., 1991; Dickens and Owen, 1999; Hermoyian and Owen, 2001;
Diester-Haass et al., 2002, 2004, 2005; Grant and Dickens, 2002; Liao and
Lyle, 2014; Lyle and Baldauf, 2015; Lyle et al., 2019). At Site 1264–1265,
the highest CaCO<inline-formula><mml:math id="M502" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content (96 %–97.5 %) occurs between <inline-formula><mml:math id="M503" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 8 and 4 Ma, and the highest bulk and CaCO<inline-formula><mml:math id="M504" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs (<inline-formula><mml:math id="M505" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 2–4.5 g cm<inline-formula><mml:math id="M506" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M507" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) are found between <inline-formula><mml:math id="M508" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.8 and 3.3 Ma (Figs. 5 and
8c), which falls within the broad timing associated with the LMBB. As
%CaCO<inline-formula><mml:math id="M509" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> is so high at Site 1264, CaCO<inline-formula><mml:math id="M510" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs account for most of
the variability in the bulk MARs. Similarly, Lyle et al. (2019) showed that the LMBB is expressed between <inline-formula><mml:math id="M511" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 8 and 4.4 Ma in the bulk and CaCO<inline-formula><mml:math id="M512" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>
MAR of six sites in the eastern equatorial Pacific (EEP), with CaCO<inline-formula><mml:math id="M513" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs
accounting for most of the bulk MAR variability (Fig. 8d). Despite the
influence of palaeogeographical heterogeneity on the absolute EEP MARs, it
becomes apparent after normalisation that common productivity patterns are
visible across the EEP (Lyle et al., 2019; Fig. 8b and d). The Site 1264 CaCO<inline-formula><mml:math id="M514" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs are generally higher than the EEP sites (Fig. 8c and d), except for ODP Sites 849 and 850, which are the two highest sedimentation EEP sites (Lyle et al., 2019).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F8" specific-use="star"><?xmltex \currentcnt{8}?><?xmltex \def\figurename{Figure}?><label>Figure 8</label><caption><p id="d1e5478">Late Miocene to present data on the new astrochronology. <bold>(a)</bold> The left axis shows XRF-derived CaCO<inline-formula><mml:math id="M515" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data from Site 1264 (dark red), and the right axis shows <inline-formula><mml:math id="M516" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 63 <inline-formula><mml:math id="M517" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>m coarse fraction (%CF)
(Keating-Bitonti and Peters, 2019). <bold>(b)</bold> Normalised Site 1264 MARs (this study) and a normalised eastern equatorial Pacific (EEP) stack comprising data from ODP Sites 848, 849, 850, and 851 and IODP Sites U1335, U1337, and U1338 (Lyle et al., 2019). <bold>(c)</bold> Site 1264 CaCO<inline-formula><mml:math id="M518" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs. <bold>(d)</bold> MARS from EEP ODP Sites 848, 849, 850, and 851 and IODP
Sites U1335 and U1338 (Lyle et al., 2019). Site U1337 is not shown here as it was partly affected by winnowing (see Lyle et al., 2019, for details).</p></caption>
          <?xmltex \igopts{width=497.923228pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/2091/2021/cp-17-2091-2021-f08.png"/>

        </fig>

      <p id="d1e5533">The exact cause of the LMBB is poorly understood; however, key hypotheses
suggest the increased primary productivity was caused by (1) increased
nutrient input into the surface ocean through increased weathering/dust
input and/or (2) changes to the global distribution of nutrients through
changes in atmospheric and oceanic circulation patterns. The widespread
documentation of the LMBB shows that the expression and timing is regionally
variable (Liao
and Lyle,<?pagebreak page2108?> 2014; Lyle et al., 2019; Sutherland et al., 2019). However, most
of these records are low resolution and insufficient for accurately
constraining regional differences, so we cannot yet distinguish between
global changes to the nutrient budget and changes to the regional
distribution of nutrients in the ocean (e.g. changes in ocean circulation
and/or upwelling). The availability of orbital-scale %CaCO<inline-formula><mml:math id="M519" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> and MARs
from Site 1264 and the EEP provide the opportunity to compare the LMBB at
high resolution for the first time. Based on increased CaCO<inline-formula><mml:math id="M520" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs, the
timing of the LMBB at Site 1264 and the EEP generally agrees well (Fig. 8b),
which corroborates the global nature of the LMBB. After increasing from 8 Ma
onwards, MARs peak between 7.2 and 6.6 Ma at both Walvis Ridge and the
equatorial Pacific (Fig. 8b), which supports a global LMBB optimum occurring
between <inline-formula><mml:math id="M521" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.0 and 6.4 Ma (Lyle
and Baldauf, 2015; Lyle et al., 2019). Site 1264 also has the highest
absolute %CaCO<inline-formula><mml:math id="M522" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> values between 7.2 and 6.6 Ma, indicating high
productivity of carbonate producers at this time (Figs. 5 and 8a). However,
the LMBB extends to 3.3 Ma at Site 1264, in contrast to the western EEP,
where the LMBB ends <inline-formula><mml:math id="M523" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 4.4 Ma (Fig. 8b). In the far eastern
equatorial Pacific near South America, high CaCO<inline-formula><mml:math id="M524" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs continue to
<inline-formula><mml:math id="M525" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 3 Ma (Fig. 8 in Lyle
et al., 2019), which is further evidence for regional variability of the
termination of the LMBB production interval. The recognition of global
patterns and temporal heterogeneity in the expression of the LMBB between
the Pacific and the Southeast Atlantic could reflect different regional
responses to a single climatic forcing and/or multiple driving forces.</p>
      <p id="d1e5595">Constraining which primary producers drove the LMBB at different regions
will be useful for disentangling regional and global patterns. During the
latest Miocene–early Pliocene (<inline-formula><mml:math id="M526" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 8–3 Ma), the new Site 1264
%CaCO<inline-formula><mml:math id="M527" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data displays an inverse relationship with the low-resolution
record of the percent <inline-formula><mml:math id="M528" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 63 <inline-formula><mml:math id="M529" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>m coarse fraction (%CF)
(Keating-Bitonti and Peters, 2019;
adapted to this study's new composite depth and age model; Figs. 5c and 8a).
The %CF specifically shows the opposite trend to %CaCO<inline-formula><mml:math id="M530" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> across
the LMBB: decreasing %CF from 8 Ma, with the lowest %CF values
occurring <inline-formula><mml:math id="M531" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7 Ma, in line with the maximum values in
%CaCO<inline-formula><mml:math id="M532" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>. Through the middle to late Miocene and early Pliocene, the LSR at
Site 1264 are either similar or higher at Site 1264 (2505 m) relative to
deeper Site 1266 (3806 m). The available %CF and %CaCO<inline-formula><mml:math id="M533" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> from Site 1264 also do not display a strong relationship prior to 8 Ma. This all suggests
that any winnowing at Site 1264 was minimal and stable for<?pagebreak page2109?> the middle to late
Miocene and early Pliocene. The inverse %CF-%CaCO<inline-formula><mml:math id="M534" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> relationship
therefore could indicate that the LMBB was predominantly driven by a change
in the calcareous phytoplankton (coccolithophores) versus foraminifera ratio
at Site 1264. Based on Si intensity, there is no evidence that biogenic
silica producers play a major role in the LMBB at Site 1264 (Fig. 5). This
contrasts with the EEP, which is upwelling dominated and where a combination
of calcareous (coccolithophores) and siliceous (diatoms) phytoplankton drove
the LMBB (Lyle
and Baldauf, 2015; Lyle et al., 2019).</p>
      <p id="d1e5673">Although we cannot yet accurately distinguish global increases in nutrient
delivery to the ocean versus the regional redistribution of nutrients
causing localised increased primary productivity, we can consider links
between this prolonged productivity event and the dynamic changes observed
during the late Miocene. Terrestrial and sea surface temperatures decreased
rapidly during the late Miocene cooling between <inline-formula><mml:math id="M535" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.0 and 5.4 Ma
(Pound
et al., 2011, 2012; Herbert et al., 2016). There is evidence for dynamic ice
sheet activity, although there is no major late Miocene increase in benthic
<inline-formula><mml:math id="M536" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O records suggesting that there was no long-term expansion
in continental ice sheet extent or substantial deep-sea cooling
(Hodell
et al., 2001; Drury et al., 2016, 2017, 2018b; Holbourn et al., 2018; Tian
et al., 2018). The carbon cycle underwent major change in the atmospheric,
terrestrial and marine realms, with evidence for an atmospheric <inline-formula><mml:math id="M537" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<inline-formula><mml:math id="M538" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula>
decrease around <inline-formula><mml:math id="M539" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 8–7 Ma (Bolton
and Stoll, 2013; Herbert et al., 2016; Mejía et al., 2017; Tanner et
al., 2020), the rise of terrestrial C<inline-formula><mml:math id="M540" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">4</mml:mn></mml:msub></mml:math></inline-formula> plants on land
(Cerling et al., 1997;
Behrensmeyer et al., 2007; Uno et al., 2016; Tauxe and Feakins, 2020) and
the globally synchronous marine late Miocene carbon isotope shift (LMCIS;
<inline-formula><mml:math id="M541" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.5–6.9 Ma) linked to global changes in oceanic circulation
(Haq et al., 1980; Hodell and Venz-Curtis, 2006; Reghellin et al., 2015, 2020; Drury et al., 2017, 2018a).</p>
      <p id="d1e5734">At Site 1264, the onset of elevated CaCO<inline-formula><mml:math id="M542" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs (<inline-formula><mml:math id="M543" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 7.8 Ma)
roughly coincides with the shift from eccentricity–precession pacing to
pervading obliquity–precession pacing of %CaCO<inline-formula><mml:math id="M544" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>, which infers an
increased influence of high-latitude processes in the Southeast Atlantic
(Fig. 5). The onset of strong obliquity pacing is also observed
<inline-formula><mml:math id="M545" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.7 Ma as asymmetric (i.e. sawtooth-shaped) benthic <inline-formula><mml:math id="M546" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O cycles, which have a characteristic “interglacial–glacial”
anti-phase relationship with benthic <inline-formula><mml:math id="M547" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">13</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>C on obliquity
timescales (Drury et al.,
2017). The appearance of strong obliquity forcing in multiple systems
shortly after 8 Ma implies increased influence of high-latitude climate
processes, such as increased glacial activity and high-latitude cooling.
There is widespread evidence that the late Miocene cooling was especially
pronounced in the high latitudes and reached near-modern gradients around
5.4 Ma (Pound et al.,
2012; Herbert et al., 2016). The growing importance of the high-latitudes in
the latest Miocene is further supported by evidence that deep-sea stable
<inline-formula><mml:math id="M548" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">13</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>C and <inline-formula><mml:math id="M549" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O switched from in-phase to anti-phase
on eccentricity timescales (Kirtland Turner, 2014; De
Vleeschouwer et al., 2020) as a result of continental carbon reservoirs
shrinking during cold periods due to increased extent of low-carbon Arctic
biomes, such as ice sheets, polar deserts and tundra
(De Vleeschouwer et al., 2020). There
is also ice-proximal evidence for enhanced glacial activity in both the
Northern Hemisphere and Southern Hemisphere, potentially indicating early transient
bipolar cryosphere activity in the latest Miocene (O'Connell
et al., 1996; Fronval and Jansen, 1996; Wolf-Welling et al., 1996; Kong et
al., 2010; Williams et al., 2010). Increased glacial weathering after 8 Ma
may have contributed to the onset of the LMBB through increased the nutrient
influx into the ocean. An increased nutrient flux may also be driven by
enhanced chemical weathering through Himalayan uplift and the
intensification of the Indian and Asian monsoon systems in the latest
Miocene (Kroon
et al., 1991; Filippelli, 1997; Zhisheng et al., 2001; Holbourn et al.,
2018; Yang et al., 2019). Finally, the LMBB may be partly driven by
increased nutrient input into the ocean as a result of widespread
continental aridification coupled with trade wind intensification due to
greater meridional gradients during the late Miocene cooling (7–5.4 Ma)
(Hovan,
1995; Filippelli, 1997; Diester-Haass et al., 2006; Tipple and Pagani, 2007;
Lyle et al., 2008; Pound et al., 2012; Herbert et al., 2016).</p>
      <p id="d1e5814">Regional variability in the LMBB may in turn be driven by regional
differences in the extent of late Miocene cooling (Pound et al., 2012;
Herbert et al., 2016), as well as regional diachrony in aridification
(Molnar,
2005; Schuster et al., 2006; Lyle et al., 2008; Dupont et al., 2013). The
LMCIS (<inline-formula><mml:math id="M550" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 7.5–6.9 Ma) has been linked to the onset of near-modern thermohaline circulation with NADW percolating further into the South
Atlantic (Hodell
and Venz-Curtis, 2006; Drury et al., 2017; Keating-Bitonti and Peters,
2019). A major shift in oceanic circulation would likewise affect the
redistribution of nutrients around the globe, thereby potentially
contributing to regional differences in nutrient supply. All these aspects
go some way to explain why the LMBB began after <inline-formula><mml:math id="M551" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 8 Ma;
however, it is unclear why the LMBB continued into the Pliocene, and
especially why it continued until 3.3 Ma at Site 1264. Further work
disentangling global versus regional productivity patterns is needed in
future to explore causal links in greater detail.</p>
</sec>
</sec>
<sec id="Ch1.S6" sec-type="conclusions">
  <label>6</label><title>Conclusions</title>
      <?pagebreak page2110?><p id="d1e5840">We present a continuous Site 1264-encompassing depth (<inline-formula><mml:math id="M552" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 316 m)
and age (<inline-formula><mml:math id="M553" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 30 Myr) model that constitutes a reference
framework for future palaeoclimatic and palaeoceanographic studies. To
achieve this framework, we generated new high-resolution (1–2 cm) XRF
records between 17 and 0 Ma at ODP Site 1264 in the Southeast Atlantic.
We used the XRF data to revise the shipboard composite splice, especially in
the late Miocene–early Pliocene interval. The new ln(Ca <inline-formula><mml:math id="M554" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) records were
integrated with previously published Oligocene–early Miocene XRF records and
calibrated to shipboard %CaCO<inline-formula><mml:math id="M555" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data to obtain the first continuous
Southeast Atlantic carbonate record spanning the last 30 million years.
Because of the variable orbital forcing imprint recorded in the Site 1264
CaCO<inline-formula><mml:math id="M556" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content, we employed three distinct tuning strategies to achieve
a 30 Myr astrochronology: (I.a) 30–9.7 Ma: CaCO<inline-formula><mml:math id="M557" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content(/benthic
<inline-formula><mml:math id="M558" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O) to eccentricity; (I.b) 9.7–8.0 Ma: CaCO<inline-formula><mml:math id="M559" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content to
<inline-formula><mml:math id="M560" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mo>(</mml:mo><mml:mi>T</mml:mi><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>; (II) 8.0–3.3 Ma: CaCO<inline-formula><mml:math id="M561" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content(/benthic <inline-formula><mml:math id="M562" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O) to
<inline-formula><mml:math id="M563" display="inline"><mml:mrow><mml:mi>E</mml:mi><mml:mi>T</mml:mi><mml:mo>-</mml:mo><mml:mi>P</mml:mi></mml:mrow></mml:math></inline-formula>; and (III) 3.3–0.0 Ma: benthic <inline-formula><mml:math id="M564" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O to LR04.</p>
      <p id="d1e5972">The %CaCO<inline-formula><mml:math id="M565" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> and CaCO<inline-formula><mml:math id="M566" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs were used to investigate carbonate
deposition in the Southeast Atlantic since the Oligocene. We recognise
three distinct orbital pacings of the short-term %CaCO<inline-formula><mml:math id="M567" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> variability,
broadly related to major changes in climate, the cryosphere and/or the
carbon cycle: (1) <inline-formula><mml:math id="M568" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 110 kyr eccentricity-driven pacing
dominates from 30 to <inline-formula><mml:math id="M569" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 13 Ma during Oligocene–Miocene global
warmth; (2) eccentricity-modulated precession-driven pacing appears after the
mMCT and prevails from 14 to 8 Ma; (3) increased obliquity–precession-driven
pacing prevails between <inline-formula><mml:math id="M570" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.7 and 3.3 Ma, following increased
influence of high-latitude processes.</p>
      <p id="d1e6024">The lowest CaCO<inline-formula><mml:math id="M571" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content (92 %–94 %) occurs between 18.5 and 14.4 Ma,
suggesting increased dissolution and/or decreased carbonate rain at Site 1264 potentially caused by the widespread global warmth associated with the
MCO. However, the beginning of the low CaCO<inline-formula><mml:math id="M572" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content at Site 1264
precedes the MCO by <inline-formula><mml:math id="M573" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1.5 Myr, in line with evidence for
dissolution-induced %CaCO<inline-formula><mml:math id="M574" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> lows in the equatorial Pacific Ocean
1.0–0.5 Myr before the MCO. This may indicate that the global warmth and
Antarctic deglaciation across the MCO was preconditioned for up to
<inline-formula><mml:math id="M575" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1.5 Myr by a prolonged interval of early Miocene global
warmth. The emergence of precession-driven pacing in the Site 1264
CaCO<inline-formula><mml:math id="M576" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content after <inline-formula><mml:math id="M577" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 14 Ma suggests that Antarctic ice
sheet expansion and global cooling across the mMCT caused regional
productivity to become more sensitive to precession forcing and/or signifies
the appearance of less corrosive deep waters at Site 1264 leading to better
preservation of precession-driven productivity cycles.</p>
      <p id="d1e6085">In association with the late Miocene Biogenic Bloom (LMBB), the highest
CaCO<inline-formula><mml:math id="M578" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> content (95 %–97.5 %) occurs between <inline-formula><mml:math id="M579" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 8 and 4 Ma and
the highest CaCO<inline-formula><mml:math id="M580" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs (<inline-formula><mml:math id="M581" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 2–4.5 g cm<inline-formula><mml:math id="M582" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> kyr<inline-formula><mml:math id="M583" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) are found
between <inline-formula><mml:math id="M584" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 7.8 and 3.3 Ma. The onset of elevated CaCO<inline-formula><mml:math id="M585" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs
(<inline-formula><mml:math id="M586" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 7.8 Ma) roughly coincides with the shift from
eccentricity–precession pacing to pervading obliquity–precession pacing of
%CaCO<inline-formula><mml:math id="M587" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>, which suggests a link between the onset of the LMBB and the
increased influence of high-latitude processes, such as enhanced glacial
activity and high-latitude cooling. The timing of the LMBB in the Site 1264
MARs agrees well with the onset in the eastern equatorial Pacific (EEP),
although the LMBB lasts <inline-formula><mml:math id="M588" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 1 Myr longer in the South Atlantic
(<inline-formula><mml:math id="M589" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 3.3 Ma) than in the EEP (<inline-formula><mml:math id="M590" display="inline"><mml:mo lspace="0mm">∼</mml:mo></mml:math></inline-formula> 4.4 Ma). Global
patterns in the LMBB may be driven by increased nutrient input through
increased late Miocene glacial weathering and/or increased weathering
associated with Himalayan uplift/intensification of the monsoon. A global
increase in the oceanic nutrient flux may be related to increased dust input
following increased continental aridification and enhanced trade winds due
to the increased latitudinal temperature gradients that appeared during the
late Miocene cooling (7–5.4 Ma). Regional differences in the expression of
the LMBB most likely reflect changes in oceanic nutrients distribution
driven by regional differences in the extent of the late Miocene cooling,
diachrony in the spread of continental aridification and/or changes in
oceanic circulation following the late Miocene carbon isotope shift.</p>
</sec>

      
      </body>
    <back><notes notes-type="dataavailability"><title>Data availability</title>

      <p id="d1e6203">All data are archived on the open-access database PANGAEA (<ext-link xlink:href="https://doi.org/10.1594/PANGAEA.919489" ext-link-type="DOI">10.1594/PANGAEA.919489</ext-link>, Drury et al., 2020). A presentation discussing this publication is available at <ext-link xlink:href="https://doi.org/10.5194/egusphere-egu21-3152" ext-link-type="DOI">10.5194/egusphere-egu21-3152</ext-link> (Drury et al., 2021a). All figures are available as high-resolution downloads, and further information (including all datasets) is also available in the Supplement.</p>
  </notes><notes notes-type="videosupplement"><title>Video supplement</title>

      <p id="d1e6215">The key findings of this publication are summarised in a webinar by Anna Joy Drury, as part of the SedsOnline Scientific Webinar series. This webinar is available at  <uri>https://www.youtube.com/watch?v=G30Eo0twx9s</uri> (last access: 4 October 2021; Drury et al., 2021b).</p>
  </notes><app-group>
        <supplementary-material position="anchor"><p id="d1e6221">A list of supplemental tables and figures is provided here.<?xmltex \hack{\newline}?><?xmltex \hack{\newline}?>
Supplementary tables:
<list list-type="bullet"><list-item>
      <p id="d1e6234">S1. Site 1264 XRF and Site 1264–1265 CaCO<inline-formula><mml:math id="M591" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data, including sedimentation
rates and all MARs. The uncalibrated Site 1264 XRF datasets and the full Site 1265
CaCO<inline-formula><mml:math id="M592" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> data are also included.</p></list-item><list-item>
      <p id="d1e6256">S2. Offsets/affine tables for Site 1264.</p></list-item><list-item>
      <p id="d1e6260">S3. Splice tie table for Site 1264.</p></list-item><list-item>
      <p id="d1e6264">S4. Mapping tables for Site 1264.</p></list-item><list-item>
      <p id="d1e6268">S5. Site 1264 to Site 1265 correlation to accommodate splice revisions.</p></list-item><list-item>
      <p id="d1e6272">S6. Selected (i.e. high-quality) bio-magnetostratigraphic events for Site 1264.</p></list-item><list-item>
      <p id="d1e6276">S7. New astrochronology (with sedimentation rates) for Site 1264</p></list-item></list>
Supplementary figures:
<list list-type="bullet"><list-item>
      <p id="d1e6283">S1. XRF intercalibration of the four measurement campaigns.</p></list-item><list-item>
      <p id="d1e6287">S2. Downcore intercalibrated XRF data from Site 1264, including ln(Ca <inline-formula><mml:math id="M593" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe), Si,
Fe, K, Ti and Mn.</p></list-item><list-item>
      <p id="d1e6298">S3. Splice revision panels for the entire interval showing revisions.</p></list-item><list-item>
      <p id="d1e6302">S4. Revisions to the off-splice mapping pairs of Core 1264B-29H.</p></list-item><list-item>
      <p id="d1e6306">S5. Generation of the composite core image of ODP Sites 1264 and 1265.</p></list-item><list-item>
      <p id="d1e6310">S6. Calibration of ln(Ca <inline-formula><mml:math id="M594" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Fe) to shipboard %CaCO<inline-formula><mml:math id="M595" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>.</p></list-item><list-item>
      <p id="d1e6330">S7. Calculation of bulk and CaCO<inline-formula><mml:math id="M596" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> MARs.</p></list-item><list-item>
      <p id="d1e6343">S8. Polynomial fit through the selected (i.e. high-quality) bio-magnetostratigraphic events for Site 1264.</p></list-item><list-item>
      <p id="d1e6347">S9. Spectral analysis of %CaCO<inline-formula><mml:math id="M597" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> on the polynomial age model.</p></list-item><list-item>
      <p id="d1e6360">S10. Oversized panels showing depth-to-age tie points and age model generation.</p></list-item><list-item>
      <p id="d1e6364">S11. Antiphase relationship between benthic <inline-formula><mml:math id="M598" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="italic">δ</mml:mi><mml:mn mathvariant="normal">18</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>O and %CaCO<inline-formula><mml:math id="M599" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>.</p></list-item></list> The supplement related to this article is available online at: <inline-supplementary-material xlink:href="https://doi.org/10.5194/cp-17-2091-2021-supplement" xlink:title="zip">https://doi.org/10.5194/cp-17-2091-2021-supplement</inline-supplementary-material>.</p></supplementary-material>
        </app-group><notes notes-type="authorcontribution"><title>Author contributions</title>

      <p id="d1e6390">AJD, DL, LJL and TW designed the study. AJD, DL, TW, HMB, LJL, NR, RHW, HP, DAH, DK, DBB and ML contributed to the data collection, processing and analysis. AJD, DL, TW and LJL contributed to the stratigraphy and astrochronology. AJD wrote the manuscript with input from all co-authors (DL, TW, HMB, DAH, NR, RHW, ML, DDB, DK, HP, LJL).</p>
  </notes><notes notes-type="competinginterests"><title>Competing interests</title>

      <p id="d1e6396">The authors declare that they have no conflict of interest.</p>
  </notes><notes notes-type="disclaimer"><title>Disclaimer</title>

      <p id="d1e6402">Publisher's note: Copernicus Publications remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p>
  </notes><ack><title>Acknowledgements</title><p id="d1e6408">This research used samples and data provided by the Ocean Drilling Program
(ODP), sponsored by the US National Science Foundation (NSF) and
participating countries. This research used data acquired at the XRF Core
Scanner Lab at the MARUM – Center for Marine Environmental Sciences,
University of Bremen, Germany. We especially thank Ursula Röhl and Vera
Lukies (MARUM) for their assistance with XRF core scanning; Alex
Wülbers, Walter Hale, and Holger Kuhlmann (IODP Bremen
Core Repository) for core handling, and Tim van Peer for valuable
discussions.  We also thank both reviewers for their constructive insights and Luc Beaufort for serving as editor.</p><p id="d1e6410">Funding for this research was provided by the Deutsche
Forschungsgemeinschaft (DFG, German Research Foundation) to Thomas Westerhold and Anna Joy Drury (project no. 242225091, 408101468). Anna Joy Drury and Diederik Liebrand were postdoctoral researchers and Heiko Pälike was the principal investigator in ERC Consolidator Grant “EARTHSEQUENCING” (grant agreement no. 617462). Anna Joy Drury is currently funded by the
European Union's Horizon 2020 research and innovation programme under the
Marie Skłodowska-Curie grant (agreement no. 796220). Diederik Liebrand is funded through the Cluster of Excellence “The Ocean Floor – Earth’s Uncharted Interface” (Research Unit Recorder), DFG grant no. 390741603. Mitch Lyle was funded by NSF grant OCE-1656960. Lucas J. Lourens's part of the research was carried out under the program of
the Netherlands Earth System Science Centre (NESSC; gravitation grant no. 024.002.001), financially supported
by the Dutch Ministry of Education, Culture and Science (OCW) through a NWO-ALW grant (project no. 865.10.001).</p></ack><notes notes-type="financialsupport"><title>Financial support</title>

      <p id="d1e6416">This research has been supported by the Deutsche Forschungsgemeinschaft (grant nos. 242225091 and 408101468), the H2020 European Research Council (grant no. 617462), European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant (grant no. 796220), the National Science Foundation (grant no. OCE-1656960), the Cluster of Excellence “The Ocean Floor – Earth’s Uncharted Interface” (Research Unit Recorder, DFG Grant Number 390741603), the Netherlands Earth System Science Centre (NESSC; gravitation grant no. 024.002.001), and the Dutch Ministry of Education, Culture and Science (OCW) through NWO-ALW grant (project no. 865.10.001).<?xmltex \hack{\newline}?><?xmltex \hack{\newline}?>The article processing charges for this open-access<?xmltex \notforhtml{\newline}?> publication were covered by the University of Bremen.</p>
  </notes><notes notes-type="reviewstatement"><title>Review statement</title>

      <p id="d1e6427">This paper was edited by Luc Beaufort and reviewed by two anonymous referees.</p>
  </notes><ref-list>
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    <!--<article-title-html>Climate, cryosphere and carbon cycle controls on Southeast Atlantic orbital-scale carbonate deposition since the Oligocene (30–0&thinsp;Ma)</article-title-html>
<abstract-html><p>The evolution of the Cenozoic cryosphere from unipolar to
bipolar over the past 30 million years (Myr) is broadly known. Highly
resolved records of carbonate (CaCO<sub>3</sub>) content provide insight into the
evolution of regional and global climate, cryosphere, and carbon cycle
dynamics. Here, we generate the first Southeast Atlantic CaCO<sub>3</sub> content
record spanning the last 30&thinsp;Myr, derived from X-ray fluorescence (XRF)
ln(Ca&thinsp;∕&thinsp;Fe) data collected at Ocean Drilling Program Site 1264 (Walvis Ridge,
SE Atlantic Ocean). We present a comprehensive and continuous depth and age
model for the entirety of Site 1264 ( ∼ &thinsp;316&thinsp;m; 30&thinsp;Myr). This
constitutes a key reference framework for future palaeoclimatic and
palaeoceanographic studies at this location. We identify three phases with
distinctly different orbital controls on Southeast Atlantic CaCO<sub>3</sub>
deposition, corresponding to major developments in climate, the cryosphere
and the carbon cycle: (1) strong  ∼ &thinsp;110&thinsp;kyr eccentricity pacing
prevails during Oligocene–Miocene global warmth ( ∼ &thinsp;30–13&thinsp;Ma), (2) increased eccentricity-modulated precession pacing appears after the middle Miocene Climate Transition (mMCT) ( ∼ &thinsp;14–8&thinsp;Ma), and (3) pervasive
obliquity pacing appears in the late Miocene ( ∼ &thinsp;7.7–3.3&thinsp;Ma)
following greater importance of high-latitude processes, such as increased
glacial activity and high-latitude cooling. The lowest CaCO<sub>3</sub> content
(92&thinsp;%–94&thinsp;%) occurs between 18.5 and 14.5&thinsp;Ma, potentially reflecting dissolution
caused by widespread early Miocene warmth and preceding Antarctic
deglaciation across the Miocene Climatic Optimum ( ∼ &thinsp;17–14.5&thinsp;Ma)
by 1.5&thinsp;Myr. The emergence of precession pacing of CaCO<sub>3</sub> deposition at
Site 1264 after  ∼ &thinsp;14&thinsp;Ma could signal a reorganisation of
surface and/or deep-water circulation in this region following Antarctic
reglaciation at the mMCT. The increased sensitivity to precession at Site 1264 between 14 and 13&thinsp;Ma is associated with an increase in mass accumulation
rates (MARs) and reflects increased regional CaCO<sub>3</sub> productivity and/or
recurrent influxes of cooler, less corrosive deep waters. The highest
carbonate content (%CaCO<sub>3</sub>) and MARs indicate that the late Miocene–early Pliocene Biogenic
Bloom (LMBB) occurs between  ∼ &thinsp;7.8 and 3.3&thinsp;Ma at Site 1264; broadly
contemporaneous with the LMBB in the equatorial Pacific Ocean. At Site 1264,
the onset of the LMBB roughly coincides with appearance of strong obliquity
pacing of %CaCO<sub>3</sub>, reflecting increased high-latitude forcing. The
global expression of the LMBB may reflect increased nutrient input into the
global ocean resulting from enhanced aeolian dust and/or glacial/chemical
weathering fluxes, due to enhanced glacial activity and increased meridional
temperature gradients. Regional variability in the timing and amplitude of
the LMBB may be driven by regional differences in cooling, continental
aridification and/or changes in ocean circulation in the late Miocene.</p></abstract-html>
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