Do Added Microplastics, Native Soil Properties, and Prevailing Climatic Conditions Have Consequences for Carbon and Nitrogen Contents in Soil? A Global Data Synthesis of Pot and Greenhouse Studies.

Microplastics threaten soil ecosystems, strongly influencing carbon (C) and nitrogen (N) contents. Interactions between microplastic properties and climatic and edaphic factors are poorly understood. We conducted a meta-analysis to assess the interactive effects of microplastic properties (type, shape, size, and content), native soil properties (texture, pH, and dissolved organic carbon (DOC)) and climatic factors (precipitation and temperature) on C and N contents in soil. We found that low-density polyethylene reduced total nitrogen (TN) content, whereas biodegradable polylactic acid led to a decrease in soil organic carbon (SOC). Microplastic fragments especially depleted TN, reducing aggregate stability, increasing N-mineralization and leaching, and consequently increasing the soil C/N ratio. Microplastic size affected outcomes; those <200 µm reduced both TN and SOC contents. Mineralization-induced nutrient losses were greatest at microplastic contents between 1 and 2.5% of soil weight. Sandy soils suffered the highest microplastic contamination-induced nutrient depletion. Alkaline soils showed the greatest SOC depletion, suggesting high SOC degradability. In low-DOC soils, microplastic contamination caused 2-fold greater TN depletion than in soils with high DOC. Sites with high precipitation and temperature had greatest decrease in TN and SOC contents. In conclusion, there are complex interactions determining microplastic impacts on soil health. Microplastic contamination always risks soil C and N depletion, but the severity depends on microplastic characteristics, native soil properties, and climatic conditions, with potential exacerbation by greenhouse emission-induced climate change.

Low carbon availability in paleosols nonlinearly attenuates temperature sensitivity of soil organic matter decomposition.

Temperature sensitivity (Q10 ) of soil organic matter (SOM) decomposition is an important parameter in models of the global carbon (C) cycle. Previous studies have suggested that substrate quality controls the intrinsic Q10 , whereas environmental factors can impose large constraints. For example, physical protection of SOM and its association with minerals attenuate the apparent Q10 through reducing substrate availability and accessibility ([S]). The magnitude of this dampening effect, however, has never been quantified. We simulated theoretical Q10 changes across a wide range of [S] and found that the relationship between Q10 and the log10 -transformed [S] followed a logistic rather than a linear function. Based on the unique Holocene paleosol chronosequence (7 soils from ca. 500 to 6900 years old), we demonstrated that the Q10 decreased nonlinearly with soil age up to 1150 years, beyond which Q10 remained stable. Hierarchical partitioning analysis indicated that an integrated C availability index, derived from principal component analysis of DOC content and parameters reflecting physical protection and mineral association, was the main explanatory variable for the nonlinear decrease of Q10 with soil age. Microbial inoculation and 13 C-labelled glucose addition showed that low C availability induced by physical protection and minerals association attenuated Q10 along the chronosequence. A separate soil incubation experiment indicated that Q10 increased exponentially with activation energy (Ea ) in the modern soil, suggesting that SOM chemical complexity regulates Q10 only when C availability is high. In conclusion, organic matter availability strongly decreased with soil age, whereas Michelis-Menten kinetics defines the Q10 response depending on C availability, but Arrhenius equation describes the effects of increasing substrate complexity.

Wildfire effects on mercury fate in soils of North-Western Siberia.

Arctic soils store 49 Gg mercury (Hg) - an extremely toxic heavy metal, whereas soil Hg can be released to the atmosphere by wildfires. For the first time we investigated the effects of wildfires on the fate of soil Hg in North-Western (NW) Siberia based on GIS maps of areas burned during the last 38 years and a field paired comparison of unburned and burned areas in tundra (mosses, lichens, some grasses, and shrubs) and forest-tundra (multi-layered canopy of larch trees, shrubs, mosses, and lichens). These field surveys were deepened by soil controlled burning to assess the Hg losses from organic horizon and mineral soil. The soil Hg stocks in the organic horizon and in the top 10 cm of the mineral soil were 3.3 ± 0.6 and 16 ± 3 mg Hg m-2 for unburned tundra and forest-tundra, respectively. After the burning by wildfires, the soil Hg stocks decreased to 2.4 ± 0.1 and 6.6 ± 0.2 mg Hg m-2 for tundra and forest-tundra, respectively. By the averages annual burned areas in NW Siberia 527 km2, wildfires in tundra and forest-tundra released 0.19 and 2.9 Mg soil Hg per year, respectively, corresponding to 28 % and 59 % of the initial soil Hg stocks. These direct effects of wildfires on Hg volatilization are raised by indirect post-pyrogenic consequences on Hg fate triggered by the vegetation succession and adsorption of atmospheric Hg on the surface of charred biomass. Charred lichens and trees accumulated 4-16 times more Hg compared to the living biomass. Blackened burned vegetation and soil reduced surface albedo and slowly increased soil temperatures in Arctic after wildfires. This created favorable conditions for seeding grasses and shrubs after wildfire and transformed burned high-latitude ecosystems into greener areas, increasing their capacity to trap atmospheric Hg by vegetation, which partly compensate the burning losses of soil Hg.