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Alternative Methods for Measuring Inorganic, Organic, and Total Dissolved Nitrogen in Soil
Author(s) -
Hood-Nowotny Rebecca,
Umaina Hinko-Najera,
Inselbacher Erich,
Oswald- Lachouani Petra,
Wanek Wolfgang
Publication year - 2010
Publication title -
soil science society of america journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.836
H-Index - 168
eISSN - 1435-0661
pISSN - 0361-5995
DOI - 10.2136/sssaj2009.0389
Subject(s) - chemistry , ammonium , soil water , dissolved organic carbon , persulfate , detection limit , environmental chemistry , nitrogen , extraction (chemistry) , nitrate , ammonium persulfate , chromatography , catalysis , organic chemistry , ecology , polymer , polymerization , biology
There are numerous methods for measuring inorganic, dissolved organic, and microbial N in soils, although many of these are complex or require expensive equipment. We have modified methods for the measurement of NH 4 + , NO 3 − , total dissolved N (TDN), and soil microbial biomass N (SMBN) in soils. The methods are based on a microtiter plate format and are rapid and simple to perform. Ammonium is quantified by a colorimetric method based on the Berthelot reaction. Total dissolved N and SMBN (by CH 3 Cl fumigation‐extraction) are quantified as NO 3 − after alkaline persulfate oxidation. Nitrate is estimated directly or after persulfate oxidation by reduction of NO 3 − to NO 2 − by VCl 3 and subsequent colorimetric determination of NO 2 − by acidic Griess reaction. The new suite of methods was compared with conventional methods such as high‐performance anion‐exchange chromatography for NO 3 − and high‐temperature catalytic oxidation for TDN. Our methods produced comparable detection limits, linearities, and precisions compared with the conventional methods. Limits of quantification were 7 μg NH 4 + –N L −1 , 55 μg NO 3 − –N L −1 , and 0.275 mg TDN L −1 The accuracy of the proposed methods was excellent, with recoveries of added NH 4 + , NO 3 − , and glycine ranging between 96 and 99%. Linearities of the respective calibrations were high ( R 2 > 0.99), and precisions for NH 4 + (CV = 2.1%), NO 3 − (CV = 3.5%), and TDN (CV = 3.9%) were comparable to the reference methods. The simplicity, rapidity, and low cost of the proposed methods therefore allow an expansion of the scope and range of N cycle studies where sophisticated instrumentation is not available.
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