“…C and N concentrations were determined by elemental analysis (NA 1500 Series 2; Carlo-Erba, Stanford, CA, USA). Ca, P and K concentrations were determined by sulphuric acid/hydrogen peroxide digestion, followed by ammonium molybdate/ascorbic acid colorimetric determination using flow injection analysis (FIAstar spectrophotometer 5023; Tecator, H€ oganas, Sweden) for P, and flame atomic absorbance spectrometry (Atomic Absorption Spectrophotometer Analyst 100; Perkin Elmer, Waltham, MA, USA) for Ca and K. Silica concentrations were assessed using an alkaline sodium hydroxide/hydrogen peroxide digest followed by determination of concentrations using flow injection analysis (Carneiro et al, 2007). Root lignin and lignin-like substances were assessed using a sulphuric acid digestion method with the remaining oven-dried, acid-insoluble residue operationally defined as the root lignin and lignin-like fraction (Woodin et al, 2009).…”