2006
DOI: 10.5194/bg-3-293-2006
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Nitrogen oxides emission from two beech forests subjected to different nitrogen loads

Abstract: Abstract. We analysed nitrogen oxides (N 2 O, NO) and carbon dioxide (CO 2 ) emissions from two beech forest soils close to Vienna, Austria, which were exposed to different nitrogen input from the atmosphere. The site Schottenwald (SW) received 20.2 kg N ha −1 y −1 and Klausenleopoldsdorf (KL) 12.6 kg N ha −1 y −1 through wet deposition. Nitric oxide emissions from soil were measured hourly with an automatic dynamic chamber system. Daily N 2 O measurements were carried out by an automatic gas sampling system. … Show more

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Cited by 89 publications
(55 citation statements)
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“…The site AB5, with high emissions, was located close to a fur farm. The long lasting extra nitrogen deposition from the farm could result in a higher nitrate availability in soil and thus higher N 2 O emissions (Kitzler et al 2006). However, the measured N-deposition during years 2003-2004 was not statistically higher in AB5 than in the other AB sites.…”
Section: Discussionmentioning
confidence: 99%
“…The site AB5, with high emissions, was located close to a fur farm. The long lasting extra nitrogen deposition from the farm could result in a higher nitrate availability in soil and thus higher N 2 O emissions (Kitzler et al 2006). However, the measured N-deposition during years 2003-2004 was not statistically higher in AB5 than in the other AB sites.…”
Section: Discussionmentioning
confidence: 99%
“…N 2 O emissions from the soil can be assumed negligible at our sites but N 2 emissions could potentially be substantial. Kitzler et al (2006) found only very low N 2 O (<0.5 Nkg/ha/year) and N 2 emissions (2.2 Nkg/ ha/year) at a comparable forest on carbonate bedrock. Much higher N 2 emission from carbonatic soils was reported by Jandl et al (2008) in a modeling study.…”
Section: Uncertaintiesmentioning
confidence: 92%
“…After gas sampling, the test tubes were opened again, soils were quantitatively retrieved, homogenized and prepared for further analyses. Gas samples were analysed within 48h as described by Kitzler et al (2006b) by automated headspace gas chromatography. Briefly, the GC was equipped with a 63Ni electron capture detector to quantify N 2 O concentrations and a flame ionization detector and a methanizer to quantify CO 2 and CH 4 concentrations.…”
Section: Measurement Of Gas Fluxes and Chemical Analysismentioning
confidence: 99%