Chaparral wildfire shifts the functional potential for soil pyrogenic organic matter and nitrogen cycling

Wildfires reshape soil microbiomes and chemistry, enhancing nitrogen availability and leaving behind pyrogenic organic matter (PyOM), a difficult to degrade carbon substrate potentially used by pyrophilous or “fire-loving” microbes. Understanding whether pyrophilous bacteria can metabolize post-fire resources is critical for predicting the fate of both carbon and nitrogen. We explored how secondary succession of pyrophilous bacteria align with changes in functional gene composition, particularly genes related to PyOM degradation and microbial nitrogen metabolism using shotgun metagenomics on 30 burned and unburned soils collected at 17, 25, 34, 131, and 376 days after a high-severity wildfire in a fire-adapted chaparral in Southern California. In burned soils, genes for PyOM degradation increased over time by 167% and for inorganic nitrogen cycling by 117%, while unburned soils showed no significant changes. Genes encoding catechol and protocatechuate, intermediates in the PyOM degradation pathway, indicate that the easier-to-degrade ortho-cleavage pathways consistently dominated the burned plots. These genes were often found alongside genes for nitrification and nitrogen retention, including assimilatory and dissimilatory nitrate reduction to ammonia (DNRA). We reconstructed 446 bacterial metagenome-assembled genomes (MAGs) and linked gene profiles to dominant taxa. Increases in genes associated with PyOM degradation and N cycling coincided with the dominance of pyrophilous Massilia and Noviherbaspirillum , which encoded distinct pathways for PyOM and inorganic N metabolism over time. Together, these findings reveal unrecognized functional shifts in bacterial communities over a high-resolution successional timeline, providing insights into the long-term impact of fire on microbial-mediated ecosystem processes that shape soil carbon and nitrogen dynamics. • Fine-scale metagenomics of post-fire soils collected at 17, 25, 34, 131, and 376 days. • Catechol and protocatechuate ortho-cleavage pathways dominated bacterial PyOM degradation in burned soils. • Nitrogen cycling genes increased in burned plots, especially those related to nitrogen retention processes. • PyOM and N genes linked to pyrophilous genera like Massilia and Noviherbaspirillum.

Authors

Institutions

Publication Details

Journal
Soil Biology and Biochemistry
Published
2025-09-21
DOI
https://doi.org/10.1016/j.soilbio.2025.109985
Citations
2
Primary Topic
Fire effects on ecosystems
Type
article
Field-Weighted Citation Impact
2.21
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Chaparral wildfire shifts the functional potential for soil pyrogenic organic matter and nitrogen cycling

Peter M. Homyak, M. Fabiola Pulido‐Chavez, Michael J. Wilkins, Amelia R. Nelson et al.
2 citations
Soil Biology and Biochemistry
Fire effects on ecosystems
2.21
article

Chaparral wildfire shifts the functional potential for soil pyrogenic organic matter and nitrogen cycling

Peter M. Homyak, M. Fabiola Pulido‐Chavez, Michael J. Wilkins, Amelia R. Nelson, Sydney I. Glassman
article en
2 citations

Abstract

Wildfires reshape soil microbiomes and chemistry, enhancing nitrogen availability and leaving behind pyrogenic organic matter (PyOM), a difficult to degrade carbon substrate potentially used by pyrophilous or “fire-loving” microbes. Understanding whether pyrophilous bacteria can metabolize post-fire resources is critical for predicting the fate of both carbon and nitrogen. We explored how secondary succession of pyrophilous bacteria align with changes in functional gene composition, particularly genes related to PyOM degradation and microbial nitrogen metabolism using shotgun metagenomics on 30 burned and unburned soils collected at 17, 25, 34, 131, and 376 days after a high-severity wildfire in a fire-adapted chaparral in Southern California. In burned soils, genes for PyOM degradation increased over time by 167% and for inorganic nitrogen cycling by 117%, while unburned soils showed no significant changes. Genes encoding catechol and protocatechuate, intermediates in the PyOM degradation pathway, indicate that the easier-to-degrade ortho-cleavage pathways consistently dominated the burned plots. These genes were often found alongside genes for nitrification and nitrogen retention, including assimilatory and dissimilatory nitrate reduction to ammonia (DNRA). We reconstructed 446 bacterial metagenome-assembled genomes (MAGs) and linked gene profiles to dominant taxa. Increases in genes associated with PyOM degradation and N cycling coincided with the dominance of pyrophilous Massilia and Noviherbaspirillum , which encoded distinct pathways for PyOM and inorganic N metabolism over time. Together, these findings reveal unrecognized functional shifts in bacterial communities over a high-resolution successional timeline, providing insights into the long-term impact of fire on microbial-mediated ecosystem processes that shape soil carbon and nitrogen dynamics. • Fine-scale metagenomics of post-fire soils collected at 17, 25, 34, 131, and 376 days. • Catechol and protocatechuate ortho-cleavage pathways dominated bacterial PyOM degradation in burned soils. • Nitrogen cycling genes increased in burned plots, especially those related to nitrogen retention processes. • PyOM and N genes linked to pyrophilous genera like Massilia and Noviherbaspirillum.

Soil Biology and BiochemistryVol. 211
University of California, Riverside (US), Colorado State University (US)
Openalex Percentile: Top 11%
Fire effects on ecosystems
2.21
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.