Enrichment of lignin-derived carbon in mineral-associated soil organic matter

Abstract

A modern paradigm of soil organic matter proposes that persistent carbon (C) derives primarily from microbial residues interacting with minerals, challenging older ideas that lignin moieties contribute to soil C because of inherent recalcitrance. We proposed that aspects of these old and new paradigms can be partially reconciled by considering interactions between lignin decomposition products and redox-sensitive iron (Fe) minerals. An Fe-rich tropical soil (with C₄ litter and either ¹³C-labeled or unlabeled lignin) was pretreated with different durations of anaerobiosis (0−12 days) and incubated aerobically for 317 days. Only 5.7 ± 0.2% of lignin ¹³C was mineralized to CO₂ versus 51.2 ± 0.4% of litter C. More added lignin-derived C (48.2 ± 0.9%) than bulk litter-derived C (30.6 ± 0.7%) was retained in mineral-associated organic matter (MAOM; density >1.8 g cm⁻³), and 12.2 ± 0.3% of lignin-derived C vs 6.4 ± 0.1% of litter C accrued in clay-sized (<2 μm) MAOM. Longer anaerobic pretreatments increased added lignin-derived C associated with Fe, according to extractions and nanoscale secondary ion mass spectrometry (NanoSIMS). Microbial residues are important, but lignin-derived C may also contribute disproportionately to MAOM relative to bulk litter-derived C, especially following redox-sensitive biogeochemical interactions.

Citation

Huang, Wenjuan; Hammel, Kenneth E.; Hao, Jialong; Thompson, Aaron; Timokhin, Vitaliy I.; Hall, Steven J. 2019. Enrichment of lignin-derived carbon in mineral-associated soil organic matter. Environmental Science & Technology. 53(13): 7522-7531. https://doi.org/10.1021/acs.est.9b01834.