14C-labeled biochar was produced by charring 14C-labeled Lolium residues. We incubated the 14C-labeled biochar in a Haplic Luvisol and in loess for 8.5聽years under controlled conditions. In total only about 6% of initially added biochar were mineralized to CO2 during the 8.5聽years. This is probably the slowest decomposition obtained experimentally for any natural organic compound. The biochar decomposition rates estimated by 14CO2 efflux between the 5th and 8th years were of 7聽脳聽10鈭? % per day. This corresponds to less than 0.3% per year under optimal conditions and is about 2.5聽times slower as reported from the previous shorter study (3.5 years).
After 3.5聽years of incubation, we analyzed 14C in dissolved organic matter, microbial biomass, and sequentially extracted neutral lipids, glycolipids, phospholipids, polysaccharides and BPCA. Biochar-derived C (14C) in microbial biomass ranged between 0.3 and 0.95% of the 14C input. Biochar-derived C in all lipid fractions was less than 1%. Over 3.5聽years, glycolipids and phospholipids were decomposed 1.6聽times faster (23% of their initial content per year) compared to neutral lipids (15%聽year鈭?). Polysaccharides contributed ca. 17% of the 14C activity in biochar. The highest portion of 14C in the initial biochar (87%) was in BPCA decreasing only 7% over 3.5聽years. Condensed aromatic moieties were the most stable fraction compared to all other biochar compounds and the high portion of BPCA in biochar explains its very high stability and its contribution to long-term C sequestration in soil.
Our new approach for analysis of biochar stability combines 14C-labeled biochar with 14C determination in chemical fractions allowed tracing of transformation products not only in released CO2 and in microbial biomass, but also evaluation of decomposition of various biochar compounds with different chemical properties.