Data from: Microplastic biodegradability does not modify plant carbon input in soil but accelerate soil carbon loss in agroecosystems
Abstract
Microplastics (MPs) are emerging contaminants that disrupt terrestrial carbon (C) cycling, yet how their biodegradability modulates the turnover of plant-derived C remains unclear. Here, we investigated how two widely used MPs—non-biodegradable polyethylene (PE) and biodegradable polylactic acid (PLA)—affected the fate of photosynthetically fixed C in dryland agroecosystem. The goal was to explore how MPs influenced C fluxes across soil-plant-atmosphere continuum (SPAC) and assess their implications on climate change.
We conducted a two-year field experiment to evaluate how PE and PLA-based MPs affected plant photosynthetic C fixation and its subsequent turnover in soil. Using 13CO2 pulse-labeling, we traced the flow of photosynthetically fixed C across the SPAC under low, medium and high MPs concentrations. We quantified: (i) 13C distribution in plant shoots, roots, and bulk soil; (ii) 13C allocation among soil aggregate size fractions; and (iii) microbial EEAs, CAZy gene abundance, and soil respiration dynamics.
Soil C sink capacity tended to decline for both MPs types, as cumulative soil CO2 emissions increased. On average, 13C retained in soil decreased from 50.8 to 41.1 mg m-2 in MPs treatments, relative to the control. Interestingly, the underlying mechanisms differed from MP types. Non-biodegradable PE-MPs weakened soil aggregation and reduced 13C retention in macro-aggregates. However, biodegradable PLA-MPs generated marginal effects on aggregation, and enhanced the activity of microbial hydrolase, which negatively affected C retention. Moreover, metagenomics confirmed that PLA-MPs enhanced microbial decomposition capacity by enriching C degradation and energy metabolism genes. Finally, photosynthetic C assimilation remained unchanged with increasing MPs concentrations, regardless of MPs types.
Synthesis and applications. Both MP types can evidently impair soil C pools and differentially alter soil C cycling via the biodegradation-dependent mechanisms. These findings challenge the widely held assumption that biodegradable MPs are inherently environmentally benign, as their presence in soils undermines C storage capacity. The findings offer insights into future applications as: 1) to phase down the increment and stock of soil MPs, in favour of truly green alternatives of plastic mulching; 2) to update the estimation methods of soil C emission in global terrestrial ecosystems considering the presence of soil MPs.
Dataset DOI: 10.5061/dryad.t76hdr8dx
Description of the data and file structure
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
PE-L: polyethylene microplastics in low concentration
PE-M: polyethylene microplastics in medium concentration
PE-H: polylactic acid microplastics in high concentration
PLA-L: polylactic acid microplastics in low concentration
PE-M: polylactic acid microplastics in medium concentration
PE-H: polylactic acid microplastics in high concentration
Data:
*13C-Shoot/Root/Soil/Respiration: 13C content in shoots, roots, soil and soil respiration (mg m-2)
*Total recovery: Total recovery of 13C (%)
*Shoots(%)/Roots(%)/Soil(%)/Respiration(%): The recovery distribution of 13C in shoots, roots, soil, and respiration (%).
*MacroC: 13C in macro-aggregates (mg m-2)
*MicroC: 13C in micro-aggregates (mg m-2)
*MicroC: 13C in silt and clay (mg m-2)
*Macrog/Microg/Siltg: Weight distribution of soil aggregates (g)
*MWD: mean weight diameter (mm)
*MBC: microbial biomass carbon (mg kg-1 soil)
*MBN: microbial biomass nitrogen (mg kg-1 soil)
*Soil enzyme activity: C-hydrolase; N-hydrolase; C-oxidase (n mol h-1 g-1)
