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The interaction of organic carbon (OC) with clay and metals stabilizes soil carbon (C), but the influence of specific clay-metal-OC assemblages (flocs) needs further evaluation. This study aimed to investigate the stability of flocs in soil as affected by external C inputs. Flocs representing OC-mineral soil fractions were synthesized using dissolved organic C (DOC) combined with kaolinite (1:1 layer structure) or montmorillonite (2:1 layer structure) clays in the absence or presence of two levels of Fe (III) (named low or high Fe). Flocs were mixed with soil (classified as Luvisol) and incubated with or without 13C labelled plant residue (i.e., ryegrass) for 30 days. The CO2 emissions and DOC concentrations as well as their 13C signatures from all treatments were examined. Total C mineralization from flocs was approximately 70% lower than non-flocced DOC. The flocs made with montmorillonite had 16–43% lower C mineralization rate than those made with kaolinite with no Fe or low Fe. However, when flocs were made with high Fe, clay mineralogy did not significantly affect total C mineralization. A positive priming effect (PE) of flocs on native soil OC was observed in all treatments, with a stronger PE found in lower Fe treatments. The high-Fe clay flocs inhibited ryegrass decomposition, while the flocs made without clay had no impact on it. Interestingly, flocs significantly decreased the PE of ryegrass on native soil OC decomposition. These results indicate that the adsorption of DOC onto clay minerals in the presence of Fe (III) stabilizes it against decomposition processes and its stability increases as Fe in flocs increases. Flocs also protect soil OC from the PE of external degradable plant C input. This study showed that Fe level and clay mineralogy play an important role in controlling soil C stability.

The continuous rise of atmospheric nitrous oxide (N2O) is an environmental issue of global concern. In biogeochemical studies, N2O production is commonly assumed to arise solely from enzymatic reactions in microbes and fungi. However, iron, manganese and organic compounds readily undergo redox reactions with intermediates in the nitrogen cycle that produce N2O abiotically under relevant environmental conditions at circumneutral pH. Although these abiotic N2O production pathways have been known to occur for close to a century, they are often neglected in modern ecological studies. In this Synthesis and Emerging Ideas paper, we highlight the defining characteristics, environmental controls, and isotopic signatures of abiotic reactions between nitrogen cycle intermediates (hydroxylamine, nitric oxide, and nitrite), redox-active metals (iron and manganese) and organic matter (humic and fulvic acids) that can lead to N2O production. We also discuss the emerging idea that abiotic reactions coupled to biotic processes have widespread ecological relevance and encourage consideration of abiotic production mechanisms in future biogeochemical investigations of N2O cycling.