Literature DB >> 16073424

Energy requirement for symbiotic nitrogen fixation.

J H Silsbury1.   

Abstract

Comparing the energy required by legumes for symbiotic nitrogen fixation with that of assimilation of nitrate, Gibson concluded the costs to be about the same. About 15% of net photosynthetic production by the plant may be used in meeting its nitrogen requirements. If energy for the fixation of nitrogen symbiotically and that for the assimilation of NH4+ or NO3- from the soil solution are both provided by the chemical products of photosynthesis, then the CO2 respired in supplying that energy must contribute to the total efflux of CO2 from the plant in the dark. McCree and Thornley have discussed methods of partitioning the dark CO2 efflux into a growth (synthesis) and a maintenance component. Both nitrogen fixation and nitrogen assimilation can be expected to contribute to the CO2 flux associated with synthesis. If Gibson is correct, nodulated plants using only symbiotically fixed nitrogen should have the same growth coefficient as non-nodulated plants supplied with exogenous mineral nitrogen when grown in the same conditions. I have examined this hypothesis using a modification of the method used by McCree with Trifolium subterraneum L. cultivar Woogenellup as test material.

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Year:  1977        PMID: 16073424     DOI: 10.1038/267149a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  8 in total

1.  Environmental and genotypic effects on the respiration associated with symbiotic nitrogen fixation in peas.

Authors:  J D Mahon
Journal:  Plant Physiol       Date:  1979-05       Impact factor: 8.340

2.  Water Stress Effects on Nitrogen Assimilation and Growth of Trifolium subterraneum L. Using Dinitrogen or Ammonium Nitrate.

Authors:  T M Dejong; D A Phillips
Journal:  Plant Physiol       Date:  1982-02       Impact factor: 8.340

3.  Economy of Carbon and Nitrogen in Nodulated and Nonnodulated (NO(3)-grown) Cowpea [Vigna unguiculata (L.) Walp.].

Authors:  C A Atkins; J S Pate; G J Griffiths; S T White
Journal:  Plant Physiol       Date:  1980-11       Impact factor: 8.340

4.  Seasonal patterns of 13C partitioning between shoots and nodulated roots of N2- or nitrate-fed Pisum sativum L.

Authors:  A S Voisin; C Salon; C Jeudy; F R Warembourg
Journal:  Ann Bot       Date:  2003-04       Impact factor: 4.357

5.  Elevated CO(2) modifies N acquisition of Medicago truncatula by enhancing N fixation and reducing nitrate uptake from soil.

Authors:  Huijuan Guo; Yucheng Sun; Yuefei Li; Xianghui Liu; Qin Ren; Keyan Zhu-Salzman; Feng Ge
Journal:  PLoS One       Date:  2013-12-05       Impact factor: 3.240

6.  Nodule carbohydrate catabolism is enhanced in the Medicago truncatula A17-Sinorhizobium medicae WSM419 symbiosis.

Authors:  Estíbaliz Larrainzar; Erena Gil-Quintana; Amaia Seminario; Cesar Arrese-Igor; Esther M González
Journal:  Front Microbiol       Date:  2014-08-27       Impact factor: 5.640

7.  Legumes Modulate Allocation to Rhizobial Nitrogen Fixation in Response to Factorial Light and Nitrogen Manipulation.

Authors:  Colleen A Friel; Maren L Friesen
Journal:  Front Plant Sci       Date:  2019-11-05       Impact factor: 5.753

8.  Soil nitrogen availability and plant genotype modify the nutrition strategies of M. truncatula and the associated rhizosphere microbial communities.

Authors:  Anouk Zancarini; Christophe Mougel; Anne-Sophie Voisin; Marion Prudent; Christophe Salon; Nathalie Munier-Jolain
Journal:  PLoS One       Date:  2012-10-15       Impact factor: 3.240

  8 in total

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