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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-22-1003-2026</article-id><title-group><article-title>Spatially contrasted response of Devonian anoxia  to astronomical forcing</article-title><alt-title>Spatially contrasted response of Devonian anoxia to astronomical forcing</alt-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes" rid="aff1">
          <name><surname>Gérard</surname><given-names>Justin</given-names></name>
          <email>justin.gerard@uclouvain.be</email>
        <ext-link>https://orcid.org/0000-0002-6477-1459</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff2">
          <name><surname>Pohl</surname><given-names>Alexandre</given-names></name>
          
        <ext-link>https://orcid.org/0000-0003-2328-351X</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Sablon</surname><given-names>Loïc</given-names></name>
          
        <ext-link>https://orcid.org/0009-0000-0489-2702</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3">
          <name><surname>Huygh</surname><given-names>Jarno</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3">
          <name><surname>Da Silva</surname><given-names>Anne-Christine</given-names></name>
          
        <ext-link>https://orcid.org/0000-0003-4191-7600</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Crucifix</surname><given-names>Michel</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-3437-4911</ext-link></contrib>
        <aff id="aff1"><label>1</label><institution>Université catholique de Louvain (UCLouvain), Earth and Life Institute (ELI), 1348 Louvain-la-Neuve, Belgium</institution>
        </aff>
        <aff id="aff2"><label>2</label><institution>Université Bourgogne Europe, CNRS, Biogéosciences UMR 6282, 21000 Dijon, France</institution>
        </aff>
        <aff id="aff3"><label>3</label><institution>University of Liège, SediCClim Department of Geology, Sart Tilman, 4000 Liége, Belgium</institution>
        </aff>
      </contrib-group>
      <author-notes><corresp id="corr1">Justin Gérard (justin.gerard@uclouvain.be)</corresp></author-notes><pub-date><day>13</day><month>May</month><year>2026</year></pub-date>
      
      <volume>22</volume>
      <issue>5</issue>
      <fpage>1003</fpage><lpage>1021</lpage>
      <history>
        <date date-type="received"><day>29</day><month>August</month><year>2025</year></date>
           <date date-type="rev-request"><day>2</day><month>September</month><year>2025</year></date>
           <date date-type="rev-recd"><day>14</day><month>April</month><year>2026</year></date>
           <date date-type="accepted"><day>16</day><month>April</month><year>2026</year></date>
      </history>
      <permissions>
        <copyright-statement>Copyright: © 2026 Justin Gérard et al.</copyright-statement>
        <copyright-year>2026</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/22/1003/2026/cp-22-1003-2026.html">This article is available from https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026.html</self-uri><self-uri xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026.pdf">The full text article is available as a PDF file from https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026.pdf</self-uri>
      <abstract><title>Abstract</title>

      <p id="d2e143">The Devonian period, spanning from 419 to 359 million years ago, was marked by a warmer-than-present climate and recurring ocean anoxic events, with evidence increasingly suggesting a link between these events and astronomical forcing. Here, we explore how astronomical forcing influences ocean oxygenation by modulating the continental weathering flux of phosphate within a Late Devonian climate framework. To investigate this, we performed transient simulations spanning 1.1 Myr, crossing a 2.4 Myr eccentricity node using the cGENIE Earth system model. These simulations were driven by spatially resolved fluxes of reactive phosphorus from continents, computed using the emulator developed by <xref ref-type="bibr" rid="bib1.bibx76" id="text.1"/>, trained on GEOCLIM and HadSM3 outputs. Our results provide new evidence supporting eccentricity maxima as a driver of Late Devonian anoxic events. Additionally, global analysis reveals that obliquity variations can leave an imprint on global ocean oxygen levels via their influence on biological productivity, suggesting a potential pathway for obliquity-driven anoxia under greenhouse conditions. Regional analysis revealed pronounced spatial heterogeneity in the biogeochemical response to astronomical forcing. Local ocean circulation emerged as a critical factor in shaping these patterns. The simulations indicate that astronomical forcing can, through its impact on continental weathering fluxes, exert a dominant influence on ocean oxygenation, with regional oxygen concentrations varying by up to 35 % and driving changes in regional anoxic volume of up to 19 %. Finally, these findings help explain why proxy records from different locations may show divergent expressions of astronomical signals, potentially leading to contrasting interpretations of their role in driving ocean anoxia.</p>
  </abstract>
    
<funding-group>
<award-group id="gs1">
<funding-source>Fonds De La Recherche Scientifique - FNRS</funding-source>
<award-id>T.0037.22</award-id>
</award-group>
<award-group id="gs2">
<funding-source>National Natural Science Foundation of China</funding-source>
<award-id>ATALTrack (VO 1276/6-1)</award-id>
<award-id>ATALTrack (BO 1829/12-1)</award-id>
</award-group>
</funding-group>
</article-meta>
  </front>
<body>
      

      
<sec id="Ch1.S1" sec-type="intro">
  <label>1</label><title>Introduction</title>
      <p id="d2e160">Throughout the Devonian Period, multiple oceanic anoxic events (OAEs) occurred <xref ref-type="bibr" rid="bib1.bibx3" id="paren.2"/>, with estimated durations ranging from 10<sup>4</sup> to 10<sup>6</sup> years <xref ref-type="bibr" rid="bib1.bibx44" id="paren.3"/>. The Late Devonian, approximately 379–360 million years ago (Ma), was particularly marked by pronounced environmental crises and ocean anoxia, such as the well-known Kellwasser and Hangenberg events <xref ref-type="bibr" rid="bib1.bibx45 bib1.bibx11" id="paren.4"/>. There is still no consensus on the mechanisms responsible for the initiation and the duration of these Devonian OAEs <xref ref-type="bibr" rid="bib1.bibx36 bib1.bibx67 bib1.bibx83" id="paren.5"/>. Existing hypotheses include extensive volcanic activity <xref ref-type="bibr" rid="bib1.bibx54 bib1.bibx61 bib1.bibx65 bib1.bibx44" id="paren.6"/>, the proliferation and expansion of terrestrial plants <xref ref-type="bibr" rid="bib1.bibx2 bib1.bibx24 bib1.bibx83" id="paren.7"/>, climate cooling <xref ref-type="bibr" rid="bib1.bibx43 bib1.bibx84 bib1.bibx38 bib1.bibx63" id="paren.8"/>, shifts in sea level and oceanic circulation dynamics <xref ref-type="bibr" rid="bib1.bibx95 bib1.bibx25 bib1.bibx14" id="paren.9"/>, and changes in the position of the continents <xref ref-type="bibr" rid="bib1.bibx9 bib1.bibx35" id="paren.10"/>. There is also growing evidence that astronomical forcing could modulate at least some of these events, primarily through a “top-down” mechanism <xref ref-type="bibr" rid="bib1.bibx11" id="paren.11"/> whereby cyclic changes in temperature and precipitation alter continental nutrient fluxes to the ocean <xref ref-type="bibr" rid="bib1.bibx23 bib1.bibx58 bib1.bibx24 bib1.bibx94 bib1.bibx41" id="paren.12"/>. Specifically, studies conducted in Poland by <xref ref-type="bibr" rid="bib1.bibx22" id="text.13"/> identified that the deposition of anoxic black shales associated with the <italic>Annulata</italic>, Dasberg, and Hangenberg events is separated by approximately 2.4 million years (Myr). This suggests a role of eccentricity in the timing of these events, as the variance spectrum of eccentricity often contains such a cycle <xref ref-type="bibr" rid="bib1.bibx50" id="paren.14"/>. However, substantial uncertainties persist regarding the phase relationship of the astronomical forcing to the onset and development of Devonian OAEs. For instance, some cyclostratigraphic interpretations have reported the occurrence of the upper Kellwasser anoxic event, after a 2.4 Myr eccentricity minima <xref ref-type="bibr" rid="bib1.bibx24 bib1.bibx19 bib1.bibx94" id="paren.15"/>, while other studies reported strong obliquity and eccentricity, resulting in marine eutrophication leading to the upper Kellwasser <xref ref-type="bibr" rid="bib1.bibx53 bib1.bibx41" id="paren.16"/>. Hence, these contrasting findings underscore the growing importance of better quantifying the contribution of astronomical forcing to Devonian oceanic oxygen levels and the pathways by which astronomical forcing may have modulated ocean oxygenation at that time.</p>
      <p id="d2e232">Our objective is to assess the impact of astronomical forcing on ocean anoxia, specifically through the modulation of continental nutrient fluxes, within a Late Devonian climate context. To this end, we performed transient simulations using the Earth system model of intermediate complexity cGENIE <xref ref-type="bibr" rid="bib1.bibx72" id="paren.17"/>, coupled offline with a continental weathering flux of nutrients. This flux is computed using an emulator trained on outputs from the general circulation model (GCM) HadSM3 <xref ref-type="bibr" rid="bib1.bibx87" id="paren.18"/> and the geochemical model GEOCLIM <xref ref-type="bibr" rid="bib1.bibx55" id="paren.19"/>, as developed in <xref ref-type="bibr" rid="bib1.bibx76" id="text.20"/>. By incorporating a GCM, we account for the changes in precipitation and evaporation caused by astronomical forcing more accurately than with the standard version of cGENIE. In addition to improving the representation of hydrological responses, this approach further enhances the simulation of nutrient fluxes to the ocean, limited in the standard cGENIE model version due to its non-dimensional treatment of continental weathering <xref ref-type="bibr" rid="bib1.bibx16" id="paren.21"/>. This modelling framework allows, on the one hand, for a mechanistic assessment of how variations in orbital parameters (namely eccentricity, precession, and obliquity) affect terrestrial weathering rates and nutrient fluxes to the ocean, thereby influencing the development and spatial extent of anoxic conditions. On the other hand, the influence of astronomical forcing on oxygen levels through changes in ocean circulation is captured by cGENIE. A detailed description of the model configuration and experimental design is presented in Sect. 2. In Sect. 3.1, we examine the global characteristics of the transient coupled simulations, followed by a regional analysis in Sect. 3.2.</p>
</sec>
<sec id="Ch1.S2">
  <label>2</label><title>Methods</title>
<sec id="Ch1.S2.SS1">
  <label>2.1</label><title>Models description</title>
      <p id="d2e265">cGENIE is an Earth system model of intermediate complexity <xref ref-type="bibr" rid="bib1.bibx15" id="paren.22"/> designed to simulate long-term interactions between climate, biogeochemical cycles, and ocean–atmosphere processes <xref ref-type="bibr" rid="bib1.bibx72" id="paren.23"/>. The ocean circulation component (3D) uses a frictional-geostrophic model to simulate the transport of heat, salinity, and biogeochemical tracers through advection, convection, and parametrised mixing. The sea ice module (2D) uses a simplified thermodynamic–dynamic scheme to compute ice thickness and fractional coverage based on thermal balances and surface flux exchanges. The atmospheric module (2D) is an energy–moisture balance layer that transports heat and humidity through advection and diffusion, with precipitation triggered by a humidity threshold. These three components form the C-GOLDSTEIN framework, fully described in <xref ref-type="bibr" rid="bib1.bibx27" id="text.24"/> and <xref ref-type="bibr" rid="bib1.bibx56" id="text.25"/>. The BIOGEM module simulates ocean biogeochemistry, including nutrient-limited biological productivity and tracer cycling, and handles air–sea gas exchange processes. The ATCHEM module tracks atmospheric chemical species and computes their partial pressures to represent changes in atmospheric composition <xref ref-type="bibr" rid="bib1.bibx72" id="paren.26"/>. For this study, we used an open-system configuration version of cGENIE with regard to carbon and phosphorus (P), which includes the SEDGEM and ROKGEM modules. SEDGEM provides a representation of sedimentary stratigraphy and the preservation of biogenic carbonates and organic carbon (C<sub>org</sub>) deposited on the seafloor <xref ref-type="bibr" rid="bib1.bibx71 bib1.bibx39" id="paren.27"/>. ROKGEM is a spatially explicit weathering module that simulates temperature- and runoff-dependent weathering rates, allowing dynamic feedbacks between climate, weathering, and the carbon cycle over multimillion-year timescales <xref ref-type="bibr" rid="bib1.bibx16" id="paren.28"/>.</p>
      <p id="d2e299">In the standard configuration of cGENIE, continental weathering is simply a function of the global mean continental temperature. This is inadequate to capture the effects of the astronomical forcing, as the latter primarily affects climate through changes in the spatial and seasonal distribution of incoming solar radiation (insolation). To address this, we replaced this simplified scheme with a state-of-the-art continental weathering module, which accounts for the coupled contributions of chemical weathering and erosion. Specifically, we used the framework described in <xref ref-type="bibr" rid="bib1.bibx76" id="text.29"/> to couple cGENIE with a climate–weathering emulator. This emulator computes weathering fluxes under varying boundary conditions (orbital parameters and <inline-formula><mml:math id="M4" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> based on statistical relationships derived from outputs of HadCM3L, HadSM3 (the latter being the slab-ocean version of HadCM3) <xref ref-type="bibr" rid="bib1.bibx87" id="paren.30"/>, and GEOCLIM (used with fixed present-day average lithological fractions), explicitly accounting for the coupled contributions of chemical weathering and physical erosion to continental weathering. Both HadCM3L and HadSM3 were used, as the 81 HadSM3 simulations used to train the emulator required heat convergence flux data obtained from HadCM3L. The weathering fluxes are instantaneously routed from continental source cells to the closest ocean coastal grid cell via a nearest-neighbour scheme, which remains suitable given the similar grid layouts, both adapted from <xref ref-type="bibr" rid="bib1.bibx79" id="text.31"/>, and the limited knowledge of the Late Devonian hydrological network. A detailed overview of GEOCLIM’s continental weathering module is presented in <xref ref-type="bibr" rid="bib1.bibx55" id="text.32"/>, while a complete description of the emulator’s architecture, training process, and topography is documented in <xref ref-type="bibr" rid="bib1.bibx76" id="text.33"/> and repeated here for clarity (see Fig. <xref ref-type="fig" rid="F1"/>).</p>

      <fig id="F1"><label>Figure 1</label><caption><p id="d2e338">Topography of the Late Devonian (370 Ma). Topography according to <xref ref-type="bibr" rid="bib1.bibx79" id="text.34"/>, reproduced from <xref ref-type="bibr" rid="bib1.bibx76" id="text.35"/>. The bathymetry is identical to the one shown in Fig. <xref ref-type="fig" rid="F2"/>b.</p></caption>
          <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f01.png"/>

        </fig>

      <p id="d2e356">The coupling between the emulator and cGENIE is deliberately minimal and targeted, replacing the continental nutrient flux of dissolved phosphate (PO<sub>4</sub>) provided by cGENIE with values computed by the emulator. This replacement is performed offline every 1000 years, a frequency that is appropriate for capturing the long-term variability caused by the astronomical forcing. All other components and processes within the model remain unchanged, as our cGENIE setup uses a simplified, single-nutrient (PO<sub>4</sub>) control on biological productivity <xref ref-type="bibr" rid="bib1.bibx72" id="paren.36"/>. In this configuration, biological productivity is driven by both [PO<sub>4</sub>] availability and local insolation. An increase in surface PO<sub>4</sub> availability stimulates biological productivity, thereby enhancing microbial oxygen consumption through remineralization in the water column. Moreover, limiting the coupling to a single flux ensures that other variables computed by ROKGEM remain unaffected, maintaining consistency and simplicity in the overall setup. As a result, cGENIE now responds to spatially-resolved, astronomically-driven variations in continental PO<sub>4</sub> flux, thereby allowing a more robust investigation of the influence of orbital forcing on ocean anoxia.</p>
      <p id="d2e409">In our simulations, the ocean is discretised on a <inline-formula><mml:math id="M11" display="inline"><mml:mrow><mml:mn mathvariant="normal">36</mml:mn><mml:mo>×</mml:mo><mml:mn mathvariant="normal">36</mml:mn></mml:mrow></mml:math></inline-formula> horizontal equal-area grid with 16 levels along the vertical that are logarithmically spaced (from 60 to 560 m). We use the continental configuration on which the emulator from <xref ref-type="bibr" rid="bib1.bibx76" id="text.37"/> was trained, namely that of <xref ref-type="bibr" rid="bib1.bibx79" id="text.38"/>, which represents the palaeogeography at 370 Ma (see Fig. <xref ref-type="fig" rid="F2"/>). As this continental reconstruction was also used in <xref ref-type="bibr" rid="bib1.bibx35" id="text.39"/>, the large-scale ocean circulation patterns and associated diagnostics described there remain valid here; in particular, the overturning circulation shows only limited sensitivity to temperature changes (see their Fig. 7c). Because the modelled climate system is older than the mid-Mesozoic advent of open-ocean planktic calcifiers (approximately 200 Ma), the representation of calcium carbonate (CaCO<sub>3</sub>) production is adapted accordingly <xref ref-type="bibr" rid="bib1.bibx69" id="paren.40"/>. Specifically, CaCO<sub>3</sub> production is restricted to shallow-marine carbonate platforms, spatially constrained based on the reconstructions of <xref ref-type="bibr" rid="bib1.bibx46" id="text.41"/>. The surface albedo and zonally averaged wind stress profiles are prescribed from the HadCM3L simulation of <xref ref-type="bibr" rid="bib1.bibx76" id="text.42"/>, conducted with the same <inline-formula><mml:math id="M14" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> (926 ppm) as in <xref ref-type="bibr" rid="bib1.bibx88" id="text.43"/> and an orbital configuration characterized by an eccentricity of 0, a longitude of perihelion of 0<inline-formula><mml:math id="M16" display="inline"><mml:mi mathvariant="italic">°</mml:mi></mml:math></inline-formula>, and an obliquity of 23<inline-formula><mml:math id="M17" display="inline"><mml:mi mathvariant="italic">°</mml:mi></mml:math></inline-formula>. These fields are incorporated into cGENIE using the open-source “muffingen” suite v0.9.24 <xref ref-type="bibr" rid="bib1.bibx70" id="paren.44"/>, and are held constant throughout the transient simulation. The solar constant is set to 1325 W m<sup>−2</sup> based on <xref ref-type="bibr" rid="bib1.bibx31" id="text.45"/>, less than today because this younger Sun was also weaker. The atmospheric oxygen concentration is set to 80 % of its present-day value to reflect the lower levels characteristic of the Late Devonian <xref ref-type="bibr" rid="bib1.bibx47 bib1.bibx59" id="paren.46"/>. The estimated climate sensitivity of cGENIE is approximately 3 °C per doubling of <inline-formula><mml:math id="M19" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub>, which is close to the mean value from the Coupled Model Intercomparison Project (CMIP) 5 and slightly lower than that from CMIP6 <xref ref-type="bibr" rid="bib1.bibx97" id="paren.47"/>. Ocean and atmosphere parameter values follow the standard cGENIE setup of <xref ref-type="bibr" rid="bib1.bibx10" id="text.48"/> and are identical to those in <xref ref-type="bibr" rid="bib1.bibx64" id="text.49"/> and in <xref ref-type="bibr" rid="bib1.bibx35" id="text.50"/>. In our setup, the empirical equation proposed by <xref ref-type="bibr" rid="bib1.bibx26" id="text.51"/> represents C<sub>org</sub> burial in marine sediments, while the empirical parameterization of <xref ref-type="bibr" rid="bib1.bibx92" id="text.52"/> accounts for redox-dependent regeneration of P from sediments. Following <xref ref-type="bibr" rid="bib1.bibx26" id="text.53"/>, C<sub>org</sub> burial scales with the flux of organic matter reaching the seafloor and is therefore a function of surface ocean productivity. Following <xref ref-type="bibr" rid="bib1.bibx92" id="text.54"/>, a significant portion of P initially bound in organic matter is degraded in surface sediments and released into the ocean as dissolved PO<sub>4</sub>. Furthermore, PO<sub>4</sub> release from sediments is enhanced under low-oxygen conditions in line with observations <xref ref-type="bibr" rid="bib1.bibx42" id="paren.55"/>. A detailed description of these schemes and their implementation in cGENIE is provided in <xref ref-type="bibr" rid="bib1.bibx39" id="text.56"/>.</p>

      <fig id="F2" specific-use="star"><label>Figure 2</label><caption><p id="d2e605">Late Devonian (370 Ma) bathymetry. Comparison between <bold>(a)</bold> the continental reconstruction from <xref ref-type="bibr" rid="bib1.bibx79" id="text.57"/>, <bold>(b)</bold> the same reconstruction interpolated onto the HadCM3L model grid used in the emulator, and <bold>(c)</bold> as per <bold>(b)</bold> on the cGENIE grid.</p></caption>
          <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f02.png"/>

        </fig>

</sec>
<sec id="Ch1.S2.SS2">
  <label>2.2</label><title>Experimental setup</title>
      <p id="d2e637">The astronomical forcing for the Devonian is not known precisely, due to the chaotic nature of the Solar System and the subtle, yet cumulative, effects of tidal dissipation on axial precession <xref ref-type="bibr" rid="bib1.bibx51" id="paren.58"/>. A series of plausible solutions is now available <xref ref-type="bibr" rid="bib1.bibx96" id="paren.59"/>, but our experiment design was finalised before that publication appeared. Nevertheless, the astronomical solution employed here shares the same frequency content and amplitude-modulation structure as those found across the Zeebe–Lantink ensemble. We adopted the same hybrid approach as <xref ref-type="bibr" rid="bib1.bibx76" id="text.60"/>. It relies, for planetary motion, on the solution by <xref ref-type="bibr" rid="bib1.bibx51" id="text.61"/> (La11a), from which we extracted the interval between 123.3 and 122.2 Ma. This interval features a resonance between the 2.4 Myr eccentricity period (associated with the <italic>g4–g3</italic> terms) and the 1.2 Myr obliquity modulation (associated with the <italic>s4–s3</italic> terms), as in most of the Cenozoic. This resonance is characterised by an increase in obliquity variance when eccentricity reaches a 2.4 Myr node, at which point its variance is lowest and the 100 000 years (kyr) component of the eccentricity signal disappears. The node occurs approximately midway through the selected interval.</p>
      <p id="d2e659">We coupled this solution with the precession model of <xref ref-type="bibr" rid="bib1.bibx80" id="text.62"/>, following the procedure outlined in <xref ref-type="bibr" rid="bib1.bibx5" id="text.63"/>. This involves first performing a harmonic decomposition of the planetary solution (using R code based on <xref ref-type="bibr" rid="bib1.bibx82" id="altparen.64"/>), and then specifying a reference obliquity and general precession rate. These reference values are given by <xref ref-type="bibr" rid="bib1.bibx28" id="text.65"/> for the period around 370 Ma. With this construction, the solution yields obliquity frequencies of 30.555 and 37.335 years, and climatic precession frequencies of 16.470 and 19.386 years, which are considered plausible for the Late Devonian. The R code used to generate these time series is available in <xref ref-type="bibr" rid="bib1.bibx18" id="text.66"/>. We verified that the time series of obliquity and longitude of perihelion are nearly identical to those obtained by integrating, forward in time, the precession model of <xref ref-type="bibr" rid="bib1.bibx49" id="text.67"/> with an appropriate Earth–Moon distance and dynamical ellipticity. The latter approach is admittedly more straightforward, but was not integrated into our workflow at the time the experiment was prepared.</p>
      <p id="d2e681">The length and choice of this specific astronomical solution reflect a compromise between representativeness and computational feasibility, given that a 1.1 Myr simulation with cGENIE requires 2 months of continuous computation on our systems. In particular, we cannot know whether the (<italic>g4–g3</italic>) versus (<italic>s4–s3</italic>) resonance was active during the Devonian, but previous cyclostratigraphic interpretations assumed a well-expressed 2.4 Myr eccentricity node and pronounced obliquity cycles when crossing the node <xref ref-type="bibr" rid="bib1.bibx24" id="paren.68"/>. The chosen solution satisfies these assumptions. Moreover, it conveniently includes within a single sequence a transition from well-expressed 100 kyr eccentricity cycles modulated by a 405 kyr cycle, to the 2.4 Myr node (during which the 100 kyr cycles disappear), and then back to well-expressed 100 kyr eccentricity cycles. For reference, we use the heliocentric convention for expressing the longitude of perihelion, which is therefore 0° when perihelion occurs in September (as in <xref ref-type="bibr" rid="bib1.bibx76" id="altparen.69"/>, and <xref ref-type="bibr" rid="bib1.bibx35" id="altparen.70"/>).</p>
      <p id="d2e699">cGENIE reached equilibrium through a two-step spin-up process similar to <xref ref-type="bibr" rid="bib1.bibx71" id="text.71"/>, <xref ref-type="bibr" rid="bib1.bibx39" id="text.72"/> and <xref ref-type="bibr" rid="bib1.bibx91" id="text.73"/>. In the initial spin-up phase (SPIN1), ocean dynamics and biogeochemical cycling equilibrate with fixed atmospheric <inline-formula><mml:math id="M25" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> and <inline-formula><mml:math id="M27" 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 under a closed system. Burial of CaCO<sub>3</sub>, C<sub>org</sub>, and P are balanced by global weathering inputs, and the resulting data are used to determine global equilibrium burial rates. The second spin-up phase (SPIN2) uses an open-system setup, with weathering fluxes set to the equilibrium with burial rates from SPIN1 and allowed to respond to temperature. A complete description of this two-step procedure in cGENIE, including C<sub>org</sub> and P feedbacks, is detailed in <xref ref-type="bibr" rid="bib1.bibx39" id="text.74"/>. We found that during the SPIN2, the model exhibited significant drift, most notably in <inline-formula><mml:math id="M31" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub>, with the system requiring up to 500 kyr to reach equilibrium. To address this, we heuristically adjusted the initial <inline-formula><mml:math id="M33" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> concentration in SPIN1 to guide the model toward a geochemically consistent Late Devonian state. Part of this consistency has already been achieved by estimating the initial mean PO<sub>4</sub> concentration based on outputs from GEOCLIM. By the end of SPIN2, the system reached an atmospheric <inline-formula><mml:math id="M36" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> concentration of approximately 550 ppm, consistent with the estimates of <xref ref-type="bibr" rid="bib1.bibx13" id="text.75"/> and <xref ref-type="bibr" rid="bib1.bibx20" id="text.76"/>, and an average surface PO<sub>4</sub> concentration of 0.47 <inline-formula><mml:math id="M39" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup>, in agreement with <xref ref-type="bibr" rid="bib1.bibx81" id="text.77"/>. Furthermore, the system achieved modern-like burial fluxes (similar to <xref ref-type="bibr" rid="bib1.bibx39" id="text.78"/>), including 0.144 PgC yr<sup>−1</sup> of CaCO<sub>3</sub> (reef only) <xref ref-type="bibr" rid="bib1.bibx29" id="paren.79"/>, 0.075 PgC yr<sup>−1</sup> of C<sub>org</sub> <xref ref-type="bibr" rid="bib1.bibx26 bib1.bibx7" id="paren.80"/>, and 0.062 Tmol yr<sup>−1</sup> of P <xref ref-type="bibr" rid="bib1.bibx4 bib1.bibx75" id="paren.81"/>. The cause of this drift remains unclear, but our testing indicates that drift is affected by the continental configuration and model resolution. A full investigation of its origin lies beyond the scope of this study, as it would require substantial computational time, with a 500 kyr simulation requiring roughly 1 month of runtime.</p>
      <p id="d2e935">Starting from the equilibrium state (SPIN2), the continental PO<sub>4</sub> nutrient flux provided by cGENIE is replaced with values computed by the emulator. The model is then run for an additional 100 kyr with astronomical parameters fixed at their average value across the adopted astronomical solution, allowing the system to adjust to the new PO<sub>4</sub> flux boundary condition. This average astronomical configuration is characterised by an eccentricity of 0.027, an obliquity of 0.388 rad (22.23°) <xref ref-type="bibr" rid="bib1.bibx28" id="paren.82"/> and longitude of perihelion set to 90° (<inline-formula><mml:math id="M48" display="inline"><mml:mrow><mml:mi>sin⁡</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mi mathvariant="italic">ϖ</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>). To ensure continuity, the global average flux of PO<sub>4</sub> computed by the emulator is rescaled (decreased by approximately 10 %) to perfectly align with the global average flux of PO<sub>4</sub> computed by the built-in weathering module of cGENIE at the end of SPIN2. Following this adaptation period, a series of 3 transient simulations spanning the full 1.1 Myr astronomical solution were conducted. These include: (1) a run with all astronomical parameters evolving (Full); (2) a sensitivity experiment with only obliquity varying while eccentricity and precession were held constant at their average values (Obli); (3) a run in which only eccentricity and precession vary, with obliquity fixed at its average value (Ecc-prec). Simulations description is summarized in Table <xref ref-type="table" rid="T1"/>. Additionally, a control simulation was performed in which all astronomical parameters were held constant at their mean values.</p>

<table-wrap id="T1" specific-use="star"><label>Table 1</label><caption><p id="d2e998"><italic>Experimental design</italic>. The type indicates whether the model operates in a closed or open configuration, with the closed setup meaning that every chemical species lost through sedimentation is compensated by an equivalent input from weathering. The emulator is the one from <xref ref-type="bibr" rid="bib1.bibx76" id="text.83"/> that is built on model outputs from HadCM3L, HadSM3, and GEOCLIM. Initial conditions (IC) for SPIN1 are derived from GEOCLIM simulations and include PO<sub>4</sub>, alkalinity (ALK), calcium, and sulfate. Forcings correspond to quantities that are explicitly prescribed during the simulations and are the same as in <xref ref-type="bibr" rid="bib1.bibx39" id="text.84"/>. Boundary conditions (BC) are derived from HadCM3L simulations as described in <xref ref-type="bibr" rid="bib1.bibx88" id="text.85"/>.</p></caption><oasis:table frame="topbot"><oasis:tgroup cols="7">
     <oasis:colspec colnum="1" colname="col1" align="left"/>
     <oasis:colspec colnum="2" colname="col2" align="left"/>
     <oasis:colspec colnum="3" colname="col3" align="left"/>
     <oasis:colspec colnum="4" colname="col4" align="right"/>
     <oasis:colspec colnum="5" colname="col5" align="left"/>
     <oasis:colspec colnum="6" colname="col6" align="left"/>
     <oasis:colspec colnum="7" colname="col7" align="left"/>
     <oasis:thead>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">Name</oasis:entry>
         <oasis:entry colname="col2">Type</oasis:entry>
         <oasis:entry colname="col3">Emulator</oasis:entry>
         <oasis:entry colname="col4">Duration (kyr)</oasis:entry>
         <oasis:entry colname="col5">IC</oasis:entry>
         <oasis:entry colname="col6">Forcings</oasis:entry>
         <oasis:entry colname="col7">BC</oasis:entry>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row>
         <oasis:entry colname="col1">SPIN1</oasis:entry>
         <oasis:entry colname="col2">Closed</oasis:entry>
         <oasis:entry colname="col3">Off</oasis:entry>
         <oasis:entry colname="col4">20</oasis:entry>
         <oasis:entry colname="col5">–</oasis:entry>
         <oasis:entry colname="col6"><inline-formula><mml:math id="M52" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub>; <inline-formula><mml:math id="M54" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>O<sub>2</sub>; surface</oasis:entry>
         <oasis:entry colname="col7">Constant wind fields</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2"/>
         <oasis:entry colname="col3"/>
         <oasis:entry colname="col4"/>
         <oasis:entry colname="col5"/>
         <oasis:entry colname="col6">flux of DIC and ALK</oasis:entry>
         <oasis:entry colname="col7">and albedo profile (HadCM3L)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">SPIN2</oasis:entry>
         <oasis:entry colname="col2">Open</oasis:entry>
         <oasis:entry colname="col3">Off</oasis:entry>
         <oasis:entry colname="col4">500</oasis:entry>
         <oasis:entry colname="col5">SPIN1</oasis:entry>
         <oasis:entry colname="col6"><inline-formula><mml:math id="M56" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>O<sub>2</sub></oasis:entry>
         <oasis:entry colname="col7">as in SPIN1</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">SPIN3</oasis:entry>
         <oasis:entry colname="col2">Open</oasis:entry>
         <oasis:entry colname="col3">On</oasis:entry>
         <oasis:entry colname="col4">100</oasis:entry>
         <oasis:entry colname="col5">SPIN2</oasis:entry>
         <oasis:entry colname="col6"><inline-formula><mml:math id="M58" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>O<sub>2</sub></oasis:entry>
         <oasis:entry colname="col7">as in SPIN1</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Full</oasis:entry>
         <oasis:entry colname="col2">Open</oasis:entry>
         <oasis:entry colname="col3">On</oasis:entry>
         <oasis:entry colname="col4">1100</oasis:entry>
         <oasis:entry colname="col5">SPIN3</oasis:entry>
         <oasis:entry colname="col6"><inline-formula><mml:math id="M60" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>O<sub>2</sub></oasis:entry>
         <oasis:entry colname="col7">as in SPIN1</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Obli</oasis:entry>
         <oasis:entry colname="col2">Open</oasis:entry>
         <oasis:entry colname="col3">On</oasis:entry>
         <oasis:entry colname="col4">1100</oasis:entry>
         <oasis:entry colname="col5">SPIN3</oasis:entry>
         <oasis:entry colname="col6"><inline-formula><mml:math id="M62" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>O<sub>2</sub></oasis:entry>
         <oasis:entry colname="col7">as in SPIN1</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Ecc-prec</oasis:entry>
         <oasis:entry colname="col2">Open</oasis:entry>
         <oasis:entry colname="col3">On</oasis:entry>
         <oasis:entry colname="col4">1100</oasis:entry>
         <oasis:entry colname="col5">SPIN3</oasis:entry>
         <oasis:entry colname="col6"><inline-formula><mml:math id="M64" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>O<sub>2</sub></oasis:entry>
         <oasis:entry colname="col7">as in SPIN1</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup></oasis:table></table-wrap>

</sec>
</sec>
<sec id="Ch1.S3">
  <label>3</label><title>Results</title>
<sec id="Ch1.S3.SS1">
  <label>3.1</label><title>Moderate global astronomical influence</title>
      <p id="d2e1360">The global time series of atmospheric <inline-formula><mml:math id="M66" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub>, oceanic PO<sub>4</sub>, and dissolved O<sub>2</sub> concentrations ([PO<sub>4</sub>] and [O<sub>2</sub>] respectively) for each transient simulation conducted across the astronomical solution are shown in Fig. <xref ref-type="fig" rid="F3"/>. Throughout the reference simulation with all astronomical parameters evolving (black line in Fig. <xref ref-type="fig" rid="F3"/>), atmospheric <inline-formula><mml:math id="M72" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> fluctuates by up to 40 ppm around a mean value of 555 ppm, driven by interactions within the open carbon cycle (ROKGEM and C<sub>org</sub> burial). In the ocean, globally-averaged [PO<sub>4</sub>] varies by approximately 0.1 <inline-formula><mml:math id="M76" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup> around a mean of 2.67 <inline-formula><mml:math id="M78" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup>, while global mean [O<sub>2</sub>] remains within a range of 5 <inline-formula><mml:math id="M81" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup> around an average of 54 <inline-formula><mml:math id="M83" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup> (see Appendix). The temporal variability of both atmospheric <inline-formula><mml:math id="M85" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> and oceanic [PO<sub>4</sub>] is almost exclusively driven by the combined forcings of eccentricity and precession, with obliquity playing a very minor role (see Fig. <xref ref-type="fig" rid="F3"/>a, b). Overall, variations in global mean concentrations caused by astronomical forcing remain of moderate amplitude. This is consistent with the results of <xref ref-type="bibr" rid="bib1.bibx76" id="text.86"/> and unsurprising considering that global averages can mask spatially heterogeneous responses, including contrasting and potentially compensating regional signals.</p>

      <fig id="F3" specific-use="star"><label>Figure 3</label><caption><p id="d2e1578">Global response to astronomical forcing. Global time series of <bold>(a)</bold> <inline-formula><mml:math id="M88" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub>, ocean <bold>(b)</bold> [PO<sub>4</sub>] and <bold>(c)</bold> [O<sub>2</sub>]. The black curve represents the simulation in which all astronomical parameters evolve. The blue curve represents the simulation with only obliquity varying, while the red curve corresponds to the simulation where only eccentricity and precession evolve. <bold>(d)</bold> The astronomical solution used in the simulations, with eccentricity in dotted red, climatic precession in red and obliquity in blue. Here, <inline-formula><mml:math id="M92" display="inline"><mml:mi>e</mml:mi></mml:math></inline-formula> denotes the eccentricity, and <inline-formula><mml:math id="M93" display="inline"><mml:mi mathvariant="italic">ϖ</mml:mi></mml:math></inline-formula> represents the longitude of perihelion.</p></caption>
          <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f03.png"/>

        </fig>

      <p id="d2e1648">Atmospheric <inline-formula><mml:math id="M94" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> and oceanic [PO<sub>4</sub>] evolve in anti-phase throughout the simulation (see black and red curves in Fig. <xref ref-type="fig" rid="F3"/>a, b). This inverse relationship occurs because intensified weathering simultaneously enhances CO<sub>2</sub> consumption and increases the continental flux of PO<sub>4</sub> to the ocean, leading to lower atmospheric <inline-formula><mml:math id="M99" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> and higher oceanic [PO<sub>4</sub>]. The dominant control of eccentricity and precession on atmospheric <inline-formula><mml:math id="M102" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> and oceanic [PO<sub>4</sub>] arises from their pronounced effect on continental weathering fluxes. Specifically, these two orbital parameters can drive changes in PO<sub>4</sub> delivery to the ocean of up to 9.5 %, compared to only about 1.5 % under obliquity-driven forcing alone. When all three orbital parameters evolve simultaneously, this modulation can reach 10.5 %. In our simulations, the dominant driver is the precession-sensitive monsoon system captured by the emulator: precession alters monsoon intensity and distribution, which directly modulates the spatial pattern of runoff and thus weathering and PO<sub>4</sub> delivery. Beyond this, eccentricity is positively correlated with PO<sub>4</sub> weathering, such that periods of high eccentricity are associated with enhanced oceanic [PO<sub>4</sub>], a feature already identified and documented in <xref ref-type="bibr" rid="bib1.bibx76" id="text.87"/>.</p>
      <p id="d2e1788">A global low-oxygen state characterises the ocean in these simulations (see Fig. <xref ref-type="fig" rid="F3"/>c) compared to the modern climate <xref ref-type="bibr" rid="bib1.bibx78 bib1.bibx30" id="paren.88"/>, consistent with the findings of <xref ref-type="bibr" rid="bib1.bibx35" id="text.89"/> under similar boundary conditions and the estimations made by <xref ref-type="bibr" rid="bib1.bibx86" id="text.90"/> based on long-term geochemical proxy data. While all three orbital parameters affect global-mean [O<sub>2</sub>], they operate through distinct mechanisms. Eccentricity and precession primarily influence global [O<sub>2</sub>] by modulating the oceanic PO<sub>4</sub> inventory. The relationship between globally-averaged [PO<sub>4</sub>] and [O<sub>2</sub>] is evidenced by a strong correlation (<inline-formula><mml:math id="M114" display="inline"><mml:mrow><mml:msup><mml:mi>R</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup><mml:mo>=</mml:mo></mml:mrow></mml:math></inline-formula> 0.82 and <inline-formula><mml:math id="M115" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value <inline-formula><mml:math id="M116" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.016)<fn id="Ch1.Footn1"><p id="d2e1876">All presented statistics account for the temporal autocorrelation inherent in our setup, using an effective sample size correction based on the <inline-formula><mml:math id="M117" display="inline"><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mi mathvariant="normal">eff</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula> method, following the approach of <xref ref-type="bibr" rid="bib1.bibx8" id="text.91"/>.</p></fn> between the two red curves in Fig. <xref ref-type="fig" rid="F3"/>b, c. These [PO<sub>4</sub>] variations arise from changes in the continental weathering flux of PO<sub>4</sub>, with high eccentricity associated with reduced global [O<sub>2</sub>]. In contrast, obliquity exerts only a very weak effect on global [PO<sub>4</sub>] that is insufficient to explain the simulated [O<sub>2</sub>] variations. This is reflected by the almost absent correlation (<inline-formula><mml:math id="M123" display="inline"><mml:mrow><mml:msup><mml:mi>R</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup><mml:mo>=</mml:mo></mml:mrow></mml:math></inline-formula> 0.06 and <inline-formula><mml:math id="M124" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value <inline-formula><mml:math id="M125" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.467) between the two blue curves in Fig. <xref ref-type="fig" rid="F3"/>b, c. Instead, obliquity primarily influences global [O<sub>2</sub>] through its strong modulation of high-latitude insolation, as also noted by <xref ref-type="bibr" rid="bib1.bibx35" id="text.92"/>. Because modelled biological productivity explicitly depends on local insolation <xref ref-type="bibr" rid="bib1.bibx72" id="paren.93"/>, obliquity substantially alters oxygen consumption in these regions. These variations lead to changes in subsurface (around 60–130 m depth) [O<sub>2</sub>] of up to 4 <inline-formula><mml:math id="M128" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup>. As these [O<sub>2</sub>] anomalies emerge in deep-water formation zones, they are efficiently distributed throughout the global ocean via large-scale overturning circulation, resulting in consistent oxygen variations of approximately 4 <inline-formula><mml:math id="M131" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup> across the benthic ocean (not shown). Consequently, times of high obliquity are associated with decreased global [O<sub>2</sub>], driven by increased biological productivity in high-latitude regions. There, the productivity anomalies driven by obliquity are more than three times larger than those caused by eccentricity and precession combined. Hence, the combination of high eccentricity and high obliquity results in the most severe depletion of simulated global [O<sub>2</sub>] (see Fig. <xref ref-type="fig" rid="F3"/>c, d).</p>
</sec>
<sec id="Ch1.S3.SS2">
  <label>3.2</label><title>High regional variability</title>
      <p id="d2e2074">To assess regional expressions of [O<sub>2</sub>] variability driven by astronomical forcing, we defined distinct regions, as shown together with their associated watersheds in Fig. <xref ref-type="fig" rid="F4"/>a and b. They are named after their approximate paleogeographic positions: region SA (South America), region WL (western Laurussia), region Si (Siberia), region NP (northern pole), and region LG (Laurussia-Gondwana). These regions were initially constrained by the depth distribution of Devonian anoxia proxy data, which predominantly originates from shallow-marine settings. Because the ocean floor from the Devonian period has been lost to subduction and plate tectonic processes, proxies for deep-water properties are scarce <xref ref-type="bibr" rid="bib1.bibx32 bib1.bibx79" id="paren.94"/>. Consequently, grid cells deeper than 1000 m were excluded, except for those associated with deep-water formation, which occurs in regions SA and NP. Within this depth-limited framework, we further refined the regions by grouping model grid points based on the temporal variance of [PO<sub>4</sub>] and [O<sub>2</sub>] (see Appendix A), with the final result shown in Fig. <xref ref-type="fig" rid="F4"/>a. Hence, this approach enables us to assess whether astronomical forcing triggers distinct biogeochemical responses across various regions.</p>

      <fig id="F4" specific-use="star"><label>Figure 4</label><caption><p id="d2e2114">Regional variation of [O<sub>2</sub>] and anoxia. <bold>(a)</bold> Definition of the five regions. <bold>(b)</bold> Watersheds based on the nearest-neighbour continental runoff routing scheme. The colour of the continental grid cell indicates in which region the weathering flux of PO<sub>4</sub> computed by the emulator of <xref ref-type="bibr" rid="bib1.bibx76" id="text.95"/> is routed. The hashed areas represent the regions as defined in cGENIE and are the same as in panel <bold>(a)</bold>. The discrepancies between the watersheds and the regions arise from the different grid resolution of cGENIE and HadSM3. <bold>(c)</bold> Time series of average oceanic [O<sub>2</sub>] anomalies and anoxic volume anomalies (in %) for each region. These quantities were computed over the full extent of each region, from the second vertical layer down to approximately 1000 m depth, excluding the surface layer as it is in equilibrium with the atmosphere. The anoxic volume is shown in a darker colour, and the anomaly is expressed as a difference of %. The anoxic threshold is set at 6.5 <inline-formula><mml:math id="M141" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup> after <xref ref-type="bibr" rid="bib1.bibx77" id="text.96"/>. For both [O<sub>2</sub>] and anoxic volume, the <inline-formula><mml:math id="M144" display="inline"><mml:mi>y</mml:mi></mml:math></inline-formula> axis scales are identical across all regional panels to allow direct comparison. As in Fig. <xref ref-type="fig" rid="F3"/>, the bottom panel displays the astronomical forcing, but shown in black for clarity.</p></caption>
          <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f04.png"/>

        </fig>

      <p id="d2e2208">Figure <xref ref-type="fig" rid="F4"/>c displays the time series of regionally-averaged [O<sub>2</sub>] and anoxic volume anomalies, for each region (as defined in Fig. <xref ref-type="fig" rid="F4"/>a), in the reference simulation with all astronomical parameters evolving concurrently (Full). The results highlight a marked spatial heterogeneity in the biogeochemical response to astronomical forcing. On the one hand, regions SA and LG exhibit strong sensitivity to astronomical variability. In these regions, [O<sub>2</sub>] fluctuates by 45 and 19.5 <inline-formula><mml:math id="M147" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup>, respectively, equivalent to a 35 % deviation from their regional means. Simulated [O<sub>2</sub>] reach their lowest values during periods of maximum eccentricity. These pronounced oxygen variations translate into substantial changes in anoxic volume, reaching approximately 19 % in region SA and 13.5 % in region LG. On the other hand, region Si is mostly unaffected by astronomical forcing. Temporal variability in both [O<sub>2</sub>] and anoxic volume is limited to approximately 5 % and 2.5 %, respectively, with the anoxic volume remaining stable throughout most of the simulation. Although the signal is subtle in magnitude, region Si exhibits an opposite precession phasing compared to regions SA and LG, a feature resulting from their locations in different hemispheres. Region NP exhibits no anoxic conditions over the period, because of its consistently high [O<sub>2</sub>] and the limited magnitude of [O<sub>2</sub>] variations, which are insufficient for any grid cell in the region to cross the anoxic threshold. These high [O<sub>2</sub>] values over region NP are expected given the presence of major deep water formation in this region, whereas the relatively weaker deep water formation in region SA explains why this region can exhibit anoxia (see Figs. <xref ref-type="fig" rid="FA1"/>e and <xref ref-type="fig" rid="FA2"/>).</p>
      <p id="d2e2305">The relative influence of individual astronomical parameters is clarified by the power spectrum analysis of the [O<sub>2</sub>] time series (Fig. <xref ref-type="fig" rid="F5"/>). Precession emerges as the dominant driver of [O<sub>2</sub>] variability in regions SA, WL, Si, and LG, while [O<sub>2</sub>] in region NP is primarily shaped by obliquity. Although eccentricity produces no distinct spectral peak, it remains essential through its modulation of precession amplitude (see Fig. <xref ref-type="fig" rid="F4"/>c). Notably, periods of high eccentricity tend to coincide with decreased oxygen levels across all regions, underscoring its consistent impact.</p>

      <fig id="F5" specific-use="star"><label>Figure 5</label><caption><p id="d2e2341">Normalized Fourier power spectrum of the regional [O<sub>2</sub>] time series. Vertical dashed lines indicate the characteristic periods of the astronomical parameters: 19 kyr for precession, 30 kyr for obliquity, and 100 and 405 kyr for eccentricity.</p></caption>
          <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f05.png"/>

        </fig>

      <p id="d2e2359">By definition, variations in anoxic volume arise from changes in regional [O<sub>2</sub>]. Typically, these [O<sub>2</sub>] fluctuations are closely tied to changes in biological productivity and subsequent demineralization. In regions SA, WL, and LG, [O<sub>2</sub>] variability is almost entirely driven by variations in the [PO<sub>4</sub>] component of biological productivity (regional <inline-formula><mml:math id="M162" 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="M163" display="inline"><mml:mo>≥</mml:mo></mml:math></inline-formula> 0.75 and <inline-formula><mml:math id="M164" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> values <inline-formula><mml:math id="M165" display="inline"><mml:mrow><mml:mo>&lt;</mml:mo><mml:msup><mml:mn mathvariant="normal">10</mml:mn><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>). In region NP, [O<sub>2</sub>] variability aligns closely with the insolation component of biological productivity (<inline-formula><mml:math id="M167" 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> = 0.66 and <inline-formula><mml:math id="M168" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value <inline-formula><mml:math id="M169" display="inline"><mml:mrow><mml:mo>&lt;</mml:mo><mml:msup><mml:mn mathvariant="normal">10</mml:mn><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>), whereas the [PO<sub>4</sub>] component shows no meaningful relationship (<inline-formula><mml:math id="M171" display="inline"><mml:mrow><mml:msup><mml:mi>R</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.01</mml:mn></mml:mrow></mml:math></inline-formula>, <inline-formula><mml:math id="M172" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value <inline-formula><mml:math id="M173" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.63). This indicates that insolation-forced biological productivity, rather than [PO<sub>4</sub>], controls [O<sub>2</sub>] dynamics in this region. Region Si exhibits a distinct behaviour compared with all others. It is the only region where [O<sub>2</sub>] variability is not primarily driven by biological productivity (<inline-formula><mml:math id="M177" display="inline"><mml:mrow><mml:msup><mml:mi>R</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.22</mml:mn></mml:mrow></mml:math></inline-formula> and <inline-formula><mml:math id="M178" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value <inline-formula><mml:math id="M179" display="inline"><mml:mrow><mml:mo>&lt;</mml:mo><mml:msup><mml:mn mathvariant="normal">10</mml:mn><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>), indicating the dominance of another mechanism. The strong correspondence between [O<sub>2</sub>] in region Si and the northern hemisphere mean (<inline-formula><mml:math id="M181" display="inline"><mml:mrow><mml:msup><mml:mi>R</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.79</mml:mn></mml:mrow></mml:math></inline-formula>, <inline-formula><mml:math id="M182" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value <inline-formula><mml:math id="M183" display="inline"><mml:mrow><mml:mo>&lt;</mml:mo><mml:msup><mml:mn mathvariant="normal">10</mml:mn><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>) suggests that large-scale physical transport and mixing, consistent with strong currents and circulation in this region (see Fig. 7), drive these regional [O<sub>2</sub>] fluctuations. Overall, our results indicate that when regional [O<sub>2</sub>] variability is high, it is primarily driven by the [PO<sub>4</sub>] component of biological productivity. However, when [PO<sub>4</sub>] fluctuations are limited, other processes, such as insolation-forced changes in biological productivity or large-scale advection and mixing, become more critical.</p>
      <p id="d2e2673">With the link between [PO<sub>4</sub>] and [O<sub>2</sub>] established, we now turn to the drivers of [PO<sub>4</sub>] variability. Figure <xref ref-type="fig" rid="F6"/> shows the time series of average [PO<sub>4</sub>] and PO<sub>4</sub> weathering, in addition to the linear regression between these two quantities for each region. Region NP has been excluded because there is no direct regional weathering flux of PO<sub>4</sub> coming from the continents. For correlation analysis, the [PO<sub>4</sub>] time series for each region (except region Si) was slightly shifted to best align with the weathering time series. This adjustment accounts for the natural time lag between the two quantities, as [PO<sub>4</sub>] typically increases when the weathering flux of PO<sub>4</sub> is high. Namely, even as continental weathering begins to decrease, [PO<sub>4</sub>] continues to rise as long as the PO<sub>4</sub> input to a given region temporarily exceeds the rate at which it is consumed, producing a lag of several thousand years between the weathering signal and the [PO<sub>4</sub>] response (see Fig. <xref ref-type="fig" rid="F6"/>). To ensure the mechanism remains consistent with an astronomical-forcing interpretation, this lag was chosen to maximize the correlation but was limited to a maximum of 5 kyr (approximately one-fourth of a precession cycle). Because both the magnitude of the PO<sub>4</sub> weathering peak and the rate at which PO<sub>4</sub> is consumed through biological productivity differ across regions, the resulting lag is region-specific. When a negative lag is applied to [PO<sub>4</sub>] in regions SA, WL, and LG, it becomes clear that regional weathering accounts for most of the variations in [PO<sub>4</sub>]. Hence, in these regions, variations in [O<sub>2</sub>] and anoxic extent are predominantly driven by regional [PO<sub>4</sub>], hence PO<sub>4</sub> weathering, which in turn is mainly modulated by eccentricity and precession (see Fig. <xref ref-type="fig" rid="F6"/>).</p>

      <fig id="F6" specific-use="star"><label>Figure 6</label><caption><p id="d2e2858">Link between continental PO<sub>4</sub> weathering flux and regional [PO<sub>4</sub>]. Displayed are correlations between regional [PO<sub>4</sub>] and their corresponding regional weathering fluxes. A negative time lag is applied in the figures on the right, where the regression is computed, and is absent from the figures on the left. Regions SA, WL, and LG have all <inline-formula><mml:math id="M210" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> values smaller than <inline-formula><mml:math id="M211" display="inline"><mml:mrow><mml:msup><mml:mn mathvariant="normal">10</mml:mn><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>, while region Si has a <inline-formula><mml:math id="M212" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value of 0.35. Region NP is excluded from the analysis due to the absence of direct continental PO<sub>4</sub> weathering.</p></caption>
          <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f06.png"/>

        </fig>

      <p id="d2e2933">In region Si, the relationship between [PO<sub>4</sub>] and PO<sub>4</sub> weathering differs fundamentally from that of all other regions. Unlike SA, WL, and LG, where regional PO<sub>4</sub> weathering clearly imprints on [PO<sub>4</sub>], no meaningful correspondence emerges in region Si. The regional PO<sub>4</sub> weathering flux is comparatively weak (about half that of region LG), and strong currents promote rapid advection and mixing, preventing local accumulation of weathered PO<sub>4</sub> (see Fig. <xref ref-type="fig" rid="F7"/>). As a result, regional [PO<sub>4</sub>] variations do not reflect local weathering input. Instead, [PO<sub>4</sub>] in region Si closely follows the broader Northern Hemisphere signal (<inline-formula><mml:math id="M222" display="inline"><mml:mrow><mml:msup><mml:mi>R</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.98</mml:mn></mml:mrow></mml:math></inline-formula> and <inline-formula><mml:math id="M223" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value <inline-formula><mml:math id="M224" display="inline"><mml:mrow><mml:mo>&lt;</mml:mo><mml:msup><mml:mn mathvariant="normal">10</mml:mn><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>), indicating that large-scale transport governs its temporal evolution. This behaviour is consistent with the mechanism identified earlier: circulation and mixing dominate both [O<sub>2</sub>] and [PO<sub>4</sub>] variability in region Si.</p>

      <fig id="F7" specific-use="star"><label>Figure 7</label><caption><p id="d2e3070">Surface ocean circulation. Mean horizontal ocean velocity (m s<sup>−1</sup>) averaged over the upper 300 m. Arrow direction indicates flow orientation, while arrow length is proportional to velocity magnitude (also represented with background shading).</p></caption>
          <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f07.png"/>

        </fig>

</sec>
</sec>
<sec id="Ch1.S4">
  <label>4</label><title>Discussion</title>
<sec id="Ch1.S4.SS1">
  <label>4.1</label><title>Implications</title>
      <p id="d2e3108">We used cGENIE with an upgraded representation of weathering taken from <xref ref-type="bibr" rid="bib1.bibx76" id="text.97"/>, to investigate the influence of astronomical forcing on Late Devonian ocean oxygenation. Our simulations show that prescribing plausible atmospheric <inline-formula><mml:math id="M228" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>O<sub>2</sub> for the Late Devonian (80 % of the modern; <xref ref-type="bibr" rid="bib1.bibx47" id="altparen.98"/>, and <xref ref-type="bibr" rid="bib1.bibx59" id="altparen.99"/>) leads to an oceanic background state already depleted in [O<sub>2</sub>], which likely contributed to the increased frequency of anoxic events observed throughout this period <xref ref-type="bibr" rid="bib1.bibx3" id="paren.100"/>. We found that astronomical forcing leaves a discernible imprint on the global time series of atmospheric <inline-formula><mml:math id="M231" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub>, oceanic [PO<sub>4</sub>], and dissolved [O<sub>2</sub>]. Notably, the evolution of atmospheric <inline-formula><mml:math id="M235" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> under astronomical forcing closely mirrors the results reported by <xref ref-type="bibr" rid="bib1.bibx76" id="text.101"/>, exhibiting a similar amplitude of approximately 40 ppm, with higher atmospheric <inline-formula><mml:math id="M237" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> concentrations corresponding to periods of minimum eccentricity. A similar <inline-formula><mml:math id="M239" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub> range was also obtained by <xref ref-type="bibr" rid="bib1.bibx91" id="text.102"/> when running cGENIE with astronomical forcing, using a very different experimental setup featuring an idealized continental configuration and no representation of C<sub>org</sub> burial. In our simulations, [O<sub>2</sub>] variations primarily occur through the influence of eccentricity and precession on continental weathering fluxes, as well as obliquity on high-latitude biological productivity. Periods of combined high eccentricity and high obliquity produce the most pronounced deoxygenation, although global mean [O<sub>2</sub>] variations remain within a modest magnitude range of 5 <inline-formula><mml:math id="M244" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup> throughout the simulations. Because the ocean exhibits substantial spatial heterogeneity in benthic [O<sub>2</sub>], with differences reaching 100 <inline-formula><mml:math id="M247" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup>, it is unlikely for the simulated [O<sub>2</sub>] variations to drive global-scale benthic areas below the anoxia threshold. Based on our modelling, it is thus highly implausible that the astronomical forcing alone could induce an anoxic event over the entire global ocean (i.e., including the benthic ocean).</p>
      <p id="d2e3325">Building on the global-scale analysis, we performed a more localized investigation by defining specific regions to capture potentially distinct biogeochemical dynamics induced by astronomical forcing. The results reveal that eccentricity maxima commonly coincide with the most pronounced anoxic extent, supporting the proposal by <xref ref-type="bibr" rid="bib1.bibx53" id="text.103"/> and <xref ref-type="bibr" rid="bib1.bibx41" id="text.104"/> that the Upper Kellwasser coincide with an eccentricity maxima configuration. However, both the magnitude and the dominant astronomical parameter driving this response vary markedly across regions, underscoring the spatial heterogeneity captured in our simulations. While certain regions exhibit strong sensitivity to astronomical forcing, with [O<sub>2</sub>] varying by up to 35 % and the anoxic volume by up to 19 %, others remain largely unaffected. Regions near continental margins (i.e., more directly influenced by weathering fluxes) exhibit a strong precessional control, with the largest variations in [O<sub>2</sub>] and anoxic volume occurring in these weathering-dominated settings. This influence is not limited to low-latitude areas; for instance, region SA exhibits a notable precession signal despite its relatively high latitude, whereas precession is generally thought to primarily affect low latitudes due to its strong control on precipitation patterns <xref ref-type="bibr" rid="bib1.bibx21" id="paren.105"/>. In contrast, high-latitude regions far from continental margins (i.e., less directly influenced by weathering fluxes) are more sensitive to obliquity-driven changes, particularly through their influence on the insolation component of biological productivity. These findings underscore the pivotal role of PO<sub>4</sub> weathering and biological productivity in shaping regional biogeochemical responses, aligning with the “top-down” hypothesis proposed in <xref ref-type="bibr" rid="bib1.bibx11" id="text.106"/>. However, physical processes such as ocean circulation and tracer advection can override this control, as exemplified in region Si, where local [O<sub>2</sub>] and [PO<sub>4</sub>] dynamics are decoupled from regional weathering due to strong transport. Our results further demonstrate how regions SA, WL and LG, characterized by relatively weak surface circulation, provide ideal conditions for astronomically driven weathering variations to leave a substantial imprint on local [O<sub>2</sub>].</p>
      <p id="d2e3395">Altogether, these results demonstrate that astronomical forcing can exert pronounced control on ocean biogeochemistry, with its impact shaped by local physical conditions. Furthermore, the regional analysis of the shallow ocean suggests that an astronomical signal may appear globally distributed across the observational record. However, it also indicates that proxy records from distinct locations may reflect fundamentally different expressions of an astronomical signal, potentially leading to contrasting interpretations of its role in driving ocean anoxia.</p>
      <p id="d2e3398">Despite the important contribution that astronomical forcing can exert on [O<sub>2</sub>], the biogeochemical response of the system remains relatively simple when compared to the forcing. Specifically, the regions often exhibit a quasi-linear response to the forcing, lacking clear signs of long-term memory effects or strong non-linearities. This is particularly surprising given that redox-dependent P regeneration is represented in our model configuration, using the scheme from <xref ref-type="bibr" rid="bib1.bibx92" id="text.107"/>, a feature explicitly proposed in <xref ref-type="bibr" rid="bib1.bibx62" id="text.108"/> to explain the sustainability of Late Devonian anoxia based on the investigation of sedimentary concentrations. Hence, the absence of prolonged anoxia in our simulations indicates that the PO<sub>4</sub> variations induced by astronomical forcing may be either too gradual or too limited in amplitude to trigger or maintain an anoxic state over extended timescales in our experimental setup (e.g., 10<sup>5</sup> years). Our results also suggest that anoxic events could manifest as a series of smaller, short-lived, precession-paced episodes (see Fig. <xref ref-type="fig" rid="F4"/>c and video in the Supplement) rather than a single, prolonged global event, similar to the scenario proposed by <xref ref-type="bibr" rid="bib1.bibx37" id="text.109"/>. These findings motivate future studies centred on additional processes that may influence the system response, including vegetation–climate interactions driven by orbital forcing and the effects of large, episodic nutrient inputs. In particular, assessing the persistence and biogeochemical consequences of such perturbations could help constrain the conditions under which sustained anoxia might emerge.</p>
</sec>
<sec id="Ch1.S4.SS2">
  <label>4.2</label><title>Limitations</title>
      <p id="d2e3448">Because cGENIE is a relatively simple model, it suffers from well-known intrinsic limitations. Among these are its coarse spatial resolution, resulting in a simplified representation of continental geometry and shallow-water environments, the absence of explicitly resolved atmospheric dynamics, a basic hydrological scheme, and the lack of ice-sheet dynamics. Nevertheless, cGENIE has been widely used in previous studies and has demonstrated its capacity to reproduce large-scale ocean circulation features <xref ref-type="bibr" rid="bib1.bibx66 bib1.bibx52 bib1.bibx10 bib1.bibx57 bib1.bibx64 bib1.bibx34 bib1.bibx48" id="paren.110"/> and to accurately simulate key aspects of ocean biogeochemistry <xref ref-type="bibr" rid="bib1.bibx72 bib1.bibx71 bib1.bibx16 bib1.bibx93 bib1.bibx1 bib1.bibx68 bib1.bibx17 bib1.bibx89 bib1.bibx60 bib1.bibx85" id="paren.111"/>. These studies collectively demonstrate the model’s reliability in simulating paleoclimate conditions and associated biogeochemical responses. Furthermore, some of these limitations are addressed by our specific experimental design. The prescribed wind stress field, although not responsive to climate variability, was derived from HadCM3L simulations conducted by <xref ref-type="bibr" rid="bib1.bibx76" id="text.112"/>. Hence, further assessments of the impact of dynamically evolving wind stress and albedo fields under astronomical forcing, through dedicated experiments specifically designed to isolate and quantify these effects, would be valuable, particularly using higher-complexity models (e.g., IPSL). This is further encouraged by the results of <xref ref-type="bibr" rid="bib1.bibx77" id="text.113"/>, who showed that astronomically driven changes in ocean circulation and ventilation can exert a strong control on oxygenation, with regional variations reaching up to 40 <inline-formula><mml:math id="M259" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup> in a Late Cretaceous context. More generally, the emulator accounts for changes in precipitation associated with variations in astronomical configuration and atmospheric <inline-formula><mml:math id="M261" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula>CO<sub>2</sub>, thereby improving the representation of hydrological controls on PO<sub>4</sub> weathering. Together, these features enable a more realistic representation of two central climate components in our study: PO<sub>4</sub> weathering and ocean circulation.</p>
      <p id="d2e3518">Still, several important limitations of our approach carry implications for interpreting the results. Our results could depend on the selected paleogeographic reconstruction, given the substantial uncertainties that persist in deep-time topography and, by extension, in slope, erosion, and weathering patterns. It would therefore be valuable for future studies to assess how alternative reconstructions, such as those from <xref ref-type="bibr" rid="bib1.bibx90" id="text.114"/> or <xref ref-type="bibr" rid="bib1.bibx12" id="text.115"/>, might influence these processes and the resulting oceanic response. Moreover, a simple nearest-neighbour scheme was used to route continental weathering products into the ocean; alternative watershed configurations could yield significantly different regional responses to astronomical forcing. Similarly, the use of HadCM3L, HadSM3, and GEOCLIM necessarily reflects one possible representation of climate and weathering dynamics; alternative emulator models or hydrological schemes could yield quantitatively different outcomes, although assessing the magnitude of such differences would require dedicated sensitivity experiments. The current setup also does not capture extreme events that may substantially influence sedimentary fluxes, and relies on a simplified organic matter sedimentation scheme that lacks oxygen dependence, highlighting the potential benefit of integrating more advanced models of organic matter diagenesis like OMEN-SED <xref ref-type="bibr" rid="bib1.bibx40" id="paren.116"/> in future work. Additionally, the surface wind stress field is held constant throughout the simulations, preventing realistic changes in circulation patterns in response to evolving astronomical configurations. The exclusion of ice sheets and sea-level variations removes critical mechanisms through which obliquity can strongly impact [O<sub>2</sub>], although the accurate representation of sea-level changes would remain challenging at the cGENIE grid resolution. Several studies have suggested that these processes may have contributed to, or exacerbated, Late Devonian anoxic events <xref ref-type="bibr" rid="bib1.bibx6 bib1.bibx14 bib1.bibx41" id="paren.117"/>. As a result, the influence of obliquity identified in this study may be underestimated, though it still leaves a discernible imprint on the global ocean. For all these reasons, we emphasize the importance of further modelling efforts to better connect orbital forcing with ocean anoxia. For instance, subsequent work would benefit from incorporating dynamic albedo and wind-stress profiles when exploring the full range of climate–circulation–biogeochemistry interactions. They could also explicitly test the robustness of the Late Devonian background state and its sensitivity to evolving external forcing across multiple models. In this context, Earth System Models of Intermediate Complexity (EMICs) offer a promising path forward, as they allow for long-timescale simulations while explicitly resolving many key physical and biogeochemical processes.</p>
</sec>
</sec>
<sec id="Ch1.S5" sec-type="conclusions">
  <label>5</label><title>Conclusions</title>
      <p id="d2e3551">We have explored the role of astronomical forcing in driving ocean anoxia under a Late Devonian climate configuration. Our experimental setup relies on an offline coupling between cGENIE and a fast climate-weathering emulator, based on a GCM, developed by <xref ref-type="bibr" rid="bib1.bibx76" id="text.118"/>. It allowed us to capture the influence of astronomical forcing on oceanic [O<sub>2</sub>] via its modulation of continental PO<sub>4</sub> weathering fluxes. At the global scale, astronomical forcing exerts a moderate impact on ocean [O<sub>2</sub>], with the most pronounced deoxygenation occurring during intervals of combined high eccentricity and high obliquity. While eccentricity and precession primarily affect [O<sub>2</sub>] through their control on PO<sub>4</sub> weathering fluxes, obliquity exerts its influence by modulating the insolation component of biological productivity at high latitudes, highlighting that even in a greenhouse world, obliquity can leave an imprint on ocean biogeochemistry, hence possibly sedimentary records. At the regional scale, eccentricity maxima also correspond to the most extensive anoxic conditions, providing new evidence supporting a strong impact of eccentricity maxima on the development of Late Devonian anoxic events. However, the biogeochemical response remains highly variable across regions. Our results show that astronomical forcing can act as a dominant control on ocean [O<sub>2</sub>], driving regional changes in anoxic volume of up to 19 %. An unanticipated result is that local ocean circulation can represent a central driver of the spatial heterogeneity in [O<sub>2</sub>] responses to astronomical forcing. As a result, sedimentary records from different locations may reflect contrasting imprints of the same astronomical signal, potentially leading to contrasting interpretations of its role in pacing Late Devonian anoxia. Finally, while this study provides insights into how astronomical forcing affects Late Devonian ocean [O<sub>2</sub>], it also stresses the difficulty of explaining the duration of Devonian anoxic events and the uncertainties in their spatial extent, underscoring that much modelling and data integration work remains to fully understand the drivers and dynamics of Late Devonian anoxia.</p>
</sec>

      
      </body>
    <back><app-group>

<app id="App1.Ch1.S1">
  <label>Appendix A</label><title>Background state and ocean circulation</title>
      <p id="d2e3641">Figure <xref ref-type="fig" rid="FA1"/>a, b, and d show a strong hemispheric asymmetry in oxygenation, with a substantially more oxygenated Northern Hemisphere compared to the Southern Hemisphere. This pattern primarily reflects large-scale ocean circulation (Fig. <xref ref-type="fig" rid="FA1"/>e), which allows well-oxygenated surface waters to ventilate the deep ocean in the Northern Hemisphere. In contrast, a pronounced oxygen minimum zone (OMZ) develops across much of the Southern Hemisphere (Fig. <xref ref-type="fig" rid="FA1"/>d), where meridional overturning circulation is nearly absent. The OMZ is shallower towards low latitudes, where primary productivity is high, consistent with enhanced biological oxygen demand (Fig. <xref ref-type="fig" rid="FA1"/>c). Primary productivity is also relatively elevated at high latitudes, while minimum values occur at mid latitudes, where downwelling associated with subtropical gyres prevents primary productivity. The seafloor [O<sub>2</sub>] map further indicates that most anoxic conditions at the seafloor are restricted to shallow ocean regions, as confirmed by comparison with the model bathymetry (Fig. <xref ref-type="fig" rid="F2"/>c). These shallow regions therefore correspond to areas where sedimentary P regeneration feedbacks are expected to be strongest.</p>

      <fig id="FA1" specific-use="star"><label>Figure A1</label><caption><p id="d2e3666">Background state at the end of SPIN3. [O<sub>2</sub>] at a depth of 600 m <bold>(a)</bold> and at the seafloor <bold>(b)</bold>. <bold>(c)</bold> Primary productivity (Pmol C yr<sup>−1</sup>). <bold>(d)</bold> Meridional average of [O<sub>2</sub>]. <bold>(e)</bold> Meridional overturning streamfunction (1 Sv <inline-formula><mml:math id="M278" display="inline"><mml:mo>≡</mml:mo></mml:math></inline-formula> 10<sup>6</sup> m<sup>3</sup> s<sup>−1</sup>). The white dashed lines in <bold>(a)</bold>, <bold>(b)</bold>, and <bold>(d)</bold> indicate the boundaries for the anoxic (A) and hypoxic (H) regions, with threshold values taken after <xref ref-type="bibr" rid="bib1.bibx77" id="text.119"/>.</p></caption>
        <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f08.png"/>

      </fig>

      <fig id="FA2" specific-use="star"><label>Figure A2</label><caption><p id="d2e3773">Deep water formation. Convective adjustments (expressed as the number of convective adjustments integrated across the water column per year) for <bold>(a)</bold> high eccentricity-high obliquity and <bold>(b)</bold> low eccentricity-low obliquity astronomical configurations.</p></caption>
        <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f09.png"/>

      </fig>

      <p id="d2e3789">Changes in ocean circulation associated with astronomical forcing are small in our simulations, with a maximum variation in overturning strength of 0.7 Sv (Sverdrup) when all orbital parameters vary together (0.56 Sv for eccentricity-precession forcing and 0.32 Sv for obliquity alone). Figure <xref ref-type="fig" rid="FA2"/> further indicates that the main regions of deep-water formation remain largely unchanged between extreme orbital configurations (extracted from the 1.1 Myr transient simulation). This small variability likely reflects the absence of dynamical changes in ocean circulation associated with orbital variations across the simulations. It may also indicate that the large-scale ocean circulation in cGENIE is not sufficiently sensitive to variations in surface albedo and wind stress forcing. Overall, the spatial distribution of deep-water formation explains the global overturning circulation pattern shown in Fig. <xref ref-type="fig" rid="FA1"/>e.</p>
</app>

<app id="App1.Ch1.S2">
  <label>Appendix B</label><title>Defining regions</title>
      <p id="d2e3805">This section clarifies how we refined the definition of the different regions based on the temporal variance of [O<sub>2</sub>] and [PO<sub>4</sub>]. Figure <xref ref-type="fig" rid="FB1"/> shows the normalized temporal variance of these two tracers, averaged over the upper 1000 m, consistent with the depth range applied in our regional analysis (see Sect. 3.2). First, a clear distinction between regions SA and WL emerges from both [O<sub>2</sub>] and [PO<sub>4</sub>] variance fields, particularly around 30° S and 60° W, providing strong justification for separating them. Second, region LG was initially split into two sub-regions based on the spatial structure of the variance fields. However, the temporal evolution and variability of [O<sub>2</sub>], anoxic volume, and [PO<sub>4</sub>] were found to be highly consistent across these sub-regions. Consequently, we merged them into a single, unified region, which we now refer to as region LG. These refinements provide a clear and consistent basis for the regional definitions presented in Fig. <xref ref-type="fig" rid="F4"/>a. Although regional boundaries are somewhat arbitrary, they follow coherent patterns of variability and are broad enough to avoid overinterpreting hyper-localised phenomena (at the single grid cell level). The resulting regions are not intended as universal classifications, but rather as a practical framework for exploring the spatial heterogeneity of climate–biogeochemical interactions.</p>

      <fig id="FB1"><label>Figure B1</label><caption><p id="d2e3869">Temporal variance. Normalized temporal variance of <bold>(a)</bold>  [O<sub>2</sub>] and <bold>(b)</bold> [PO<sub>4</sub>] averaged over the upper 1000 m. Dashed coloured lines indicate regional boundaries, as defined in Fig. <xref ref-type="fig" rid="F4"/>.</p></caption>
        
        <graphic xlink:href="https://cp.copernicus.org/articles/22/1003/2026/cp-22-1003-2026-f10.png"/>

      </fig>


</app>
  </app-group><notes notes-type="codeavailability"><title>Code availability</title>

      <p id="d2e3912">The code for the version of the “muffin” release of the cGENIE Earth system model used in this paper, is tagged as v0.9.72, and is assigned a DOI: <ext-link xlink:href="https://doi.org/10.5281/zenodo.19682719" ext-link-type="DOI">10.5281/zenodo.19682719</ext-link> <xref ref-type="bibr" rid="bib1.bibx74" id="paren.120"/>. Configuration files for the specific experiments presented in the paper can be found in the directory: genie-userconfigs/PUBS/published/Gerard_et_al_2025. Details of the experiments, plus the command line needed to run each one, are given in the “readme.txt” file in that directory. All other configuration files and boundary conditions are provided as part of the code release. A manual detailing code installation, basic model configuration, tutorials covering various aspects of model configuration, experimental design, and output, plus the processing of results, is assigned the following DOI: <ext-link xlink:href="https://doi.org/10.5281/zenodo.13377225" ext-link-type="DOI">10.5281/zenodo.13377225</ext-link>
<xref ref-type="bibr" rid="bib1.bibx73" id="paren.121"/>.</p>
  </notes><notes notes-type="dataavailability"><title>Data availability</title>

      <p id="d2e3930">No datasets were used in this article.</p>
  </notes><notes notes-type="videosupplement"><title>Video supplement</title>

      <p id="d2e3936">Spatial [O<sub>2</sub>] anomaly (bottom), averaged from the second vertical layer down to approximately 1000 m depth, evolving through the 1.1 Myr astronomical solution (top). Dashed lines indicate the percentage of the water column (up to 1000 m) below the anoxic threshold of 6.5 <inline-formula><mml:math id="M291" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol kg<sup>−1</sup>. The red dot represents climatic precession, the red cross eccentricity, and the blue dot obliquity. Periods of reduced [O<sub>2</sub>] appear as distinct pulses rather than a single prolonged event. For instance, severe deoxygenation is particularly evident at 0.15 and 0.98 Myr. The video is available at <ext-link xlink:href="https://doi.org/10.5446/73022" ext-link-type="DOI">10.5446/73022</ext-link> <xref ref-type="bibr" rid="bib1.bibx33" id="paren.122"/>.</p>
  </notes><app-group>
        <supplementary-material position="anchor"><p id="d2e3984">The supplement related to this article is available online at <inline-supplementary-material xlink:href="https://doi.org/10.5194/cp-22-1003-2026-supplement" xlink:title="zip">https://doi.org/10.5194/cp-22-1003-2026-supplement</inline-supplementary-material>.</p></supplementary-material>
        </app-group><notes notes-type="authorcontribution"><title>Author contributions</title>

      <p id="d2e3993">JG conducted the cGENIE experiments, developed the code for the analysis, performed all computations, and drafted the manuscript. AP contributed to the development of the open setup configuration of cGENIE. MC and ACDS contributed to the study design. All authors contributed to the discussion of results, writing the manuscript and approved the final version.</p>
  </notes><notes notes-type="competinginterests"><title>Competing interests</title>

      <p id="d2e3999">The contact author has declared that none of the authors has any competing interests.</p>
  </notes><ack><title>Acknowledgements</title><p id="d2e4006">Computational resources have been provided by the supercomputing facilities of the Université catholique de Louvain (CISM/UCL) and the Consortium des Équipements de Calcul Intensif en Fédération Wallonie Bruxelles (CÉCI).</p></ack><notes notes-type="financialsupport"><title>Financial support</title>

      <p id="d2e4011">This research has been supported by the Fonds De La Recherche Scientifique – FNRS, project WarmAnoxia (grant no. T.0037.22). AP acknowledges the support of the French Agence Nationale de la Recherche (ANR) (reference no. ANR-23-CE01-0003, project CYCLO-SED).</p>
  </notes><notes notes-type="reviewstatement"><title>Review statement</title>

      <p id="d2e4017">This paper was edited by Yannick Donnadieu and reviewed by Alexander Farnsworth and one anonymous referee.</p>
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