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15N natural abundance studies in Australian commercial sugarcane
Authors:Biggs  Ian M.  Stewart  George R.  Wilson  John R.  Critchley  Christa
Affiliation:(1) Department of Botany, The University of Queensland, St Lucia, Qld, 4072, Australia;(2) Present address: CSIRO Division of Sustainable Ecosystems, 120 Meiers Road, Indooroopilly, Qld, 4068, Australia
Abstract:The measurement of natural 15N abundance is a well-established technique for the identification and quantification of biological N2 fixation in plants. Associative N2 fixing bacteria have been isolated from sugarcane and reported to contribute potentially significant amounts of N to plant growth and development. It has not been established whether Australian commercial sugarcane receives significant input from biological N2 fixation, even though high populations of N2 fixing bacteria have been isolated from Australian commercial sugarcane fields and plants. In this study, delta15N measurements were used as a primary measure to identify whether Australian commercial sugarcane was obtaining significant inputs of N via biological N2 fixation. Quantification of N input, via biological N2 fixation, was not possible since suitable non-N2 fixing reference plants were not present in commercial cane fields. The survey of Australian commercially grown sugarcane crops showed the majority had positive leaf delta15N values (73% >3.00permil, 63% of which were >5.00permil), which was not indicative of biological N2 fixation being the major source of N for these crops. However, a small number of sites had low or negative leaf delta15N values. These crops had received high N fertiliser applications in the weeks prior to sampling. Two possible pathways that could result in low delta15N values for sugarcane leaves (other than N2 fixation) are proposed; high external N concentrations and foliar uptake of volatilised NH3. The leaf delta15N value of sugarcane grown in aerated solution culture was shown to decrease by approximately 5permil with increasing external N concentration (0.5–8.0 mM), with both NO3 and NH4+ nitrogen forms. Foliar uptake of atmospheric NH3 has been shown to result in depleted leaf delta15N values in many plant species. Acid traps collected atmospheric N with negative delta15N value (–24.45±0.90permil) from above a field recently surface fertilised with urea. The delta15N of leaves of sugarcane plants either growing directly in the soil or isolated from soil in pots dropped by 3.00permil in the same field after the fertiliser application. Both the high concentration of external N in the root zone (following the application of N-fertilisers) and/or subsequent foliar uptake of volatilised NH3 could have caused the depleted leaf delta15N values measured in the sugarcane crops at these sites.
Keywords:nitrogen metabolism    /content/x77vna7ln2h99fm2/xxlarge948.gif"   alt="  delta"   align="  BASELINE"   BORDER="  0"  >15N  Saccharum spp.  N2 fixation
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