Abstract

Abstract. Phosphorus is often invoked as the ultimate limiting nutrient, modulating primary productivity on geological timescales. Consequently, along with nitrogen, phosphorus bioavailability exerts a fundamental control on organic carbon production, linking all the biogeochemical cycles across the Earth system. Unlike nitrogen that can be microbially fixed from an essentially infinite atmospheric reservoir, phosphorus availability is dictated by the interplay between its sources and sinks. While authigenic apatite formation has received considerable attention as the dominant sedimentary phosphorus sink, the quantitative importance of reduced iron-phosphate minerals, such as vivianite, has only recently been acknowledged, and their importance remains underexplored. Combining microscopic and spectroscopic analyses of handpicked mineral aggregates with sediment geochemical profiles, we characterize the distribution and mineralogy of iron-phosphate minerals present in methane-rich sediments recovered from the northern South China Sea. Here, we demonstrate that vivianite authigenesis is pervasive in the iron-oxide-rich sediments below the sulfate–methane transition zone (SMTZ). We hypothesize that the downward migration of the SMTZ concentrated vivianite formation below the current SMTZ. Our observations support recent findings from non-steady-state post-glacial sedimentary successions, suggesting that iron reduction below the SMTZ, probably driven by iron-mediated anaerobic oxidation of methane (Fe-AOM), is coupled to phosphorus cycling on a much greater spatial scale than previously assumed. Calculations reveal that vivianite acts as an important burial phase for both iron and phosphorus below the SMTZ, sequestering approximately half of the total reactive iron pool. By extension, sedimentary vivianite formation could serve as a mineralogical marker of Fe-AOM, signalling low-sulfate availability against methanogenic and ferruginous backdrop. Given that similar conditions were likely present throughout vast swathes of Earth's history, it is possible that Fe-AOM and vivianite authigenesis may have modulated methane and phosphorus availability on the early Earth, as well as during later periods of expanded marine oxygen deficiency. A better understanding of vivianite authigenesis, therefore, is fundamental to test long-standing hypotheses linking climate, atmospheric chemistry and the evolution of the biosphere.

Highlights

  • Phosphorus (P) is an essential nutrient, and its availability limits primary production on both short and long timescales (Algeo and Ingall, 2007; Ruttenberg, 2014)

  • We stress that we do not advocate this approach to replace porewater analysis but, in its absence, we argue that porewater data from nearby sites, when combined with solid-phase distributions from Site 973-4, allow us to estimate the approximate position of the sulfate–methane transition zone (SMTZ), albeit with caveats

  • Combining bulk geochemical extractions with microscopic and spectroscopic analyses of handpicked mineral aggregates, we show that vivianite formation occurs within the iron- and methane-rich sediments from the Taixinan Basin, South China Sea

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Summary

Introduction

Phosphorus (P) is an essential nutrient, and its availability limits primary production on both short and long timescales (Algeo and Ingall, 2007; Ruttenberg, 2014). Through a combination of organic matter remineralization and reductive dissolution of Fe-oxides, PO4 is released into the sediment porewater where precipitation of P-bearing minerals has the potential to sequester P over potentially geologically relevant timescales (Jensen et al, 1995; Ruttenberg and Berner, 1993; Sundby et al, 1992). Authigenic carbonate fluorapatite (CFA) is typically assumed to be the dominant sedimentary P mineral, accounting for around half of global marine P burial (Ruttenberg, 2014). Another potentially important group of P burial phases, which have only recently been recognized, are Fe(II)-phosphate minerals such as vivianite (Fe3(PO4)2 · 8H2O). The global importance of these phosphates, remains under-constrained

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