Analytes Certified for in 2022
This method is required to adjust soil chemical results based on air-dry samples to an oven-dry (105oC)
basis. When the air-dry moisture content (M%) is known, the correction from air-dry
to oven-dry is as follows:
Oven-dry result = [Air-dry result x (100+ M%)]/100
Initially, milled air-dry soil is extracted for 1 h with 2M KCl at a 1:10 soil/solution ratio. For 7C1a to 7C1h methods, mineral-N components are quantified by steam distillations and subsequent titrations. For 7C2 methods, mineral-N fractions in the clarified soil extract are determined by automated colorimetric procedures. Ammonium ions (NH4+) are measured by a modified Berthelot indophenol reaction, while the Griess-Ilosvay reaction is used for NO3-N (and NO2-N). The methods specify reporting results for NH4-N and NO3-N [plus NO2-N if present], respectively, as mg N/kg on an oven-dry (105oC) basis. Specifically, method 7C2a relates to an automated colour, continuous segmented flow analytical finish, while Method 7C2b codes an automated colour finish by flow injection analysis. Little difference is expected in results due to choice of colorimetric finish.
This test on milled air-dry sample at a soil/water ratio of 1:5 for 1 h is suitable for use on all soils, irrespective of whether acidic or alkaline. It usually underestimates the soluble salt status of soils containing natural or added gypsum, particularly if ³ 1% of gypsum is present. Such soils would have an EC of about 2 dS/m. Soil EC x 0.336 (Method 3B1) approximates percent total soluble salts, while approximate soil ionic strength (Method 3C1) at 0.1 bar (I0.1) can be calculated as follows: I0.1 = [0.0446*EC1:5 – 0.000173], where I0.1 has units of mM, and EC1:5 has units of dS/m @ 25oC.
Analysis of Mehlich 3 extract using inductively-coupled atomic emission spectroscopy (ICP-AES)
This method for total soil OC involves production, purification and measurement of CO2 evolved when soil carbon is ignited in a stream of O2. Because all C compounds are converted to CO2, the C from carbonates, charcoal, undecomposed wood, etc, will be included, as no soil pre-treatment is specified. In the volumetric sub-method 6B2a, concentrated KOH solution is used to absorb the CO2 released. The difference between the original volume of gas in the burette and the volume produced after ignition equals the volume of CO2 evolved from the sample, after correction for gas temperature and pressure. Sub-method 6B2b is similar to Method 6B2a, except the CO2 produced by ignition is measured via infrared / thermal conductivity detection. Both 6B2a and 6B2b use finely-milled air-dry sample, with weights varying with expected C concentrations. Surrogate estimates can be obtained by NIR (method 6B4a) or MIR (method 6B4b) reflectance spectroscopy. The methods specify reporting as %C on an oven-dry (105oC) basis.
Following quantitative action / pre-treatment to account for or to physically remove (if present) charcoal and to chemically remove carbonate with excess 5% H2SO3 solution on a hot plate in a fume cabinet, the residual, re-dried soil sample is analysed for soil C by a suitable method, preferably Method 6B2b. The method involving carbonate removal and soil C analysis uses finely-milled air-dry sample, with weights varying with expected C concentrations. The method specifies reporting as %C on an oven-dry (105oC) basis.
Microwave digestion - open system without HF, and final medium HNO3/peroxide. ICP-AES finish.
Finely divided dry sample. Dumas combustion.