<p>Trace elements and isotopes (TEIs) are important to marine life and are essential tools for studying ocean processes<sup><CitationRef CitationID="CR1">1</CitationRef></sup>. Two different frameworks have arisen regarding marine TEI cycling: reversible scavenging favours water-column control on TEI distributions<sup><CitationRef AdditionalCitationIDS="CR3 CR4" CitationID="CR2">2</CitationRef>–<CitationRef CitationID="CR5">5</CitationRef></sup>, and seafloor boundary exchange emphasizes sedimentary imprints on water-column biogeochemistry<sup><CitationRef CitationID="CR6">6</CitationRef>,<CitationRef CitationID="CR7">7</CitationRef></sup>. These two views lead to disparate interpretations of TEI behaviours<sup><CitationRef AdditionalCitationIDS="CR9" CitationID="CR8">8</CitationRef>–<CitationRef CitationID="CR10">10</CitationRef></sup>. Here we use rare earth elements and neodymium isotopes as exemplar tracers of particle scavenging<sup><CitationRef CitationID="CR11">11</CitationRef></sup> and boundary exchange<sup><CitationRef CitationID="CR6">6</CitationRef>,<CitationRef CitationID="CR7">7</CitationRef>,<CitationRef CitationID="CR12">12</CitationRef></sup>. We integrate these data with models of particle cycling and sediment diagenesis to propose a general framework for marine TEI cycling. We show that, for elements with greater affinity for manganese oxide than biogenic particles, scavenging is a net sink throughout the water column, contrary to a common assumption for reversible scavenging<sup><CitationRef CitationID="CR3">3</CitationRef>,<CitationRef CitationID="CR13">13</CitationRef></sup>. In this case, a benthic flux supports increasing elemental concentrations with water depth. This sedimentary source consists of two components: one recycled from elements scavenged by water-column particles, and another newly introduced to the water column through marine silicate weathering inside sediment<sup><CitationRef CitationID="CR8">8</CitationRef>,<CitationRef CitationID="CR14">14</CitationRef>,<CitationRef CitationID="CR15">15</CitationRef></sup>. Abyssal oxic diagenesis drives this benthic source, and exerts a strong influence on water-column biogeochemistry through seafloor geometry and bottom-intensified turbulent mixing<sup><CitationRef CitationID="CR16">16</CitationRef>,<CitationRef CitationID="CR17">17</CitationRef></sup>. Our findings affirm the role of authigenic minerals, often overshadowed by biogenic particles, in water-column cycling<sup><CitationRef CitationID="CR18">18</CitationRef></sup>, and suggest that the abyssal seafloor, often regarded as inactive, is a focus of biogeochemical transformation<sup><CitationRef CitationID="CR19">19</CitationRef>,<CitationRef CitationID="CR20">20</CitationRef></sup>.</p>

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Abyssal seafloor as a key driver of ocean trace-metal biogeochemical cycles

  • Jianghui Du,
  • Brian A. Haley,
  • James McManus,
  • Patrick Blaser,
  • Jörg Rickli,
  • Derek Vance

摘要

Trace elements and isotopes (TEIs) are important to marine life and are essential tools for studying ocean processes1. Two different frameworks have arisen regarding marine TEI cycling: reversible scavenging favours water-column control on TEI distributions25, and seafloor boundary exchange emphasizes sedimentary imprints on water-column biogeochemistry6,7. These two views lead to disparate interpretations of TEI behaviours810. Here we use rare earth elements and neodymium isotopes as exemplar tracers of particle scavenging11 and boundary exchange6,7,12. We integrate these data with models of particle cycling and sediment diagenesis to propose a general framework for marine TEI cycling. We show that, for elements with greater affinity for manganese oxide than biogenic particles, scavenging is a net sink throughout the water column, contrary to a common assumption for reversible scavenging3,13. In this case, a benthic flux supports increasing elemental concentrations with water depth. This sedimentary source consists of two components: one recycled from elements scavenged by water-column particles, and another newly introduced to the water column through marine silicate weathering inside sediment8,14,15. Abyssal oxic diagenesis drives this benthic source, and exerts a strong influence on water-column biogeochemistry through seafloor geometry and bottom-intensified turbulent mixing16,17. Our findings affirm the role of authigenic minerals, often overshadowed by biogenic particles, in water-column cycling18, and suggest that the abyssal seafloor, often regarded as inactive, is a focus of biogeochemical transformation19,20.