Nitrogen isotope analysis of free glycine in soil using isotope dilution mass spectrometry [An article from: Soil Biology and Biochemistry]
Book Details
PublisherElsevier
ISBN / ASINB000PC0K9O
ISBN-13978B000PC0K95
AvailabilityAvailable for download now
MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from Soil Biology and Biochemistry, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
To enable the estimation of production and consumption rates of free glycine in soils through ^1^5N isotope dilution experiments, an isotope dilution mass spectrometric method was developed. The method, which enabled high precision N isotope ratio determination of glycine in soil extracts at @d^1^5N levels up to 4000%% and concentrations from approximately 2@mM, is based on the following steps: (i) addition of glycine spike to the soil extract, (ii) removal of humic substances and pre-concentration of glycine using solid phase extraction, (iii) derivatization of amino acids, (iv) separation of the derivatives using gas chromatography (GC), (v) their combustion to yield sample N"2 gas, and (vi) finally the use of N isotope ratio mass spectrometry (IRMS). Judging by uncertainty budget calculations, the precision obtained (SD=0.01-0.06at% ^1^5N) is sufficient for detecting differences in N isotopic ratios obtained in ^1^5N isotope dilution experiments.
Description:
To enable the estimation of production and consumption rates of free glycine in soils through ^1^5N isotope dilution experiments, an isotope dilution mass spectrometric method was developed. The method, which enabled high precision N isotope ratio determination of glycine in soil extracts at @d^1^5N levels up to 4000%% and concentrations from approximately 2@mM, is based on the following steps: (i) addition of glycine spike to the soil extract, (ii) removal of humic substances and pre-concentration of glycine using solid phase extraction, (iii) derivatization of amino acids, (iv) separation of the derivatives using gas chromatography (GC), (v) their combustion to yield sample N"2 gas, and (vi) finally the use of N isotope ratio mass spectrometry (IRMS). Judging by uncertainty budget calculations, the precision obtained (SD=0.01-0.06at% ^1^5N) is sufficient for detecting differences in N isotopic ratios obtained in ^1^5N isotope dilution experiments.
