Data from: Degradable versus inert microplastics: Effects on soil organic carbon persistence via microbial drivers in an agroecosystem
Abstract
Microplastics (MPs) are widespread in terrestrial ecosystems, raising global concerns that they may disrupt soil organic carbon (SOC) cycling and undermine agroecosystem contributions to climate mitigation. Yet it remains unclear how degradable versus inert MPs affect microbially mediated SOC stabilization.
We conducted a field experiment in a dryland agroecosystem using polyethylene (PE; inert) and polylactic acid (PLA; degradable) MPs at three residue levels, integrating metagenomics with SOC fractionation, microbial necromass quantification, and extracellular enzyme stoichiometry to resolve microbial pathways underpinning SOC persistence.
PE and PLA-MPs exerted contrasting effects on SOC stabilization. PE-MPs intensified microbial C limitation, enriched Actinobacteria, and increased the abundance of carbohydrate-degrading CAZy families, thereby accelerating decomposition and reducing particulate organic C by 10.5-16.7%; concomitantly, PE-MPs constrained microbial necromass formation and depleted SOC. In contrast, PLA-MPs increased labile C availability, stimulated C and N metabolic pathways and amino sugar metabolism. These responses enhanced microbial necromass formation by 3.6-6.9% and increased exopolysaccharide synthesis, ultimately promoting mineral-associated organic C accumulation.
Collectively, these polymer-specific microbial responses demonstrate how plastic residues can either weaken or reinforce soil C persistence, with implications for forecasting agroecosystem C sinks and guiding plastic substitution and residue management under climate relevant land stewardship.
https://doi.org/10.5061/dryad.zkh1893rz
Files and variables
File: DATA.csv
All raw data associated with the figures have been compiled in the file DATA.csv.
Notes:
Treatment:
- CT: control, no addition of microplastic
- PE1: polyethylene microplastics in low concentration
- PE2: polyethylene microplastics in medium concentration
- PE3: polylactic acid microplastics in high concentration
- PLA1: polylactic acid microplastics in low concentration
- PLA2: polylactic acid microplastics in medium concentration
- PLA3: polylactic acid microplastics in high concentration
Variables:
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POC: C contents of particulate organic carbon (g kg-1)
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MAOC: C contents of mineral-associated organic carbon (g kg-1)
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13C-POC: 13C in particulate organic carbon (mg m-2)
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13C-MAOC: 13C in mineral-associated organic carbon (mg m-2)
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FN: Fungal necromass (g kg-1)
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BN: Bacterial necromass (g kg-1)
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VL: Vector length (Unitless index derived from ratios of C-, N-, and P-acquiring extracellular enzyme activities. Because it is calculated from enzyme activity ratios or relative proportions, the original enzyme activity units cancel out. Higher vector length indicates stronger relative microbial C limitation)
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BG/AP: The ratio of β-glucosidase activity to acid phosphatase activity. This dimensionless ratio represents relative investment in C- versus P-acquiring enzymes (unitless).
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BG/(NAG+LAP): The ratio of B-glucosidase activity to the summed activities of N-acetylglucosaminidase and leucine aminopeptidase (unitless).
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CR: Cumulative respiration (mg CO2-C g-1 SOC)
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SHANNON: Shannon diversity was calculated from the taxonomic abundance table derived from metagenomic annotation and used to represent overall microbial taxonomic α-diversity (calculated using relative abundances; therefore, no physical unit applies)
