Stable isotope techniques can be used as a tool in nitrogen cycling studies of different ecosystems. The studies are based on measurement of the heavy (15N)- to- light (14N) isotopic ratios of nitrogen in different biospheric pools. Isotope ratio mass spectrometry (IRMS) is the most precise technique to use for analysis of nitrogen isotopic ratios. This thesis deals with the development of methods for compound-specific nitrogen isotope analysis of ammonium and glycine in aqueous solutions and soil extracts using Gas Chromatography - Combustion (GC-C) - IRMS. For ammonium, three different techniques were developed: equilibrium headspace analysis, solid phase microextraction (SPME) and the purge and trap (P & T) technique, which were all based on conversion of ammonium to ammonia with subsequent separation of ammonia for analysis. In the SPME and P & T approaches, custom-made absorbents were used for pre-concentration, followed by thermal desorption into the GC-C-IRMS system. For the equilibrium headspace technique, high precision measurements of the nitrogen isotopic ratio were obtained for concentrations above 420 mg N L-1. With further improvements and the use of suitable equipment, the method has the potential to be used for solutions containing ammonium in the low mg N L-1 range. The SPME technique increased the sensitivity by a factor of » 3 compared to the headspace technique, but was less precise. In addition, the NafionÒ material used for absorption showed a memory effect in the desorption step. With the P & T technique a large variation in the measured isotopic value was observed (using solutions containing 2 mg N L-1) which was due to a non-quantitative thermal desorption. However, with further improvements, the P & T technique has the potential to be used for samples containing below 1.0 µg N, which is a much lower amount than that possible with any method used today. A method for determination of the nitrogen isotopic ratio in free glycine in soil extract