Literature DB >> 15558328

Role of nutrient level and defoliation on symbiotic function: experimental evidence by tracing 14C/15N exchange in mycorrhizal birch seedlings.

Minna-Maarit Kytöviita1.   

Abstract

High nutrient availability and defoliation generally reduce ectomycorrhizal colonization levels in trees, but it is not known how this affects the functional aspects of mycorrhizal symbiosis. It was therefore investigated whether (1) defoliation or increasing substrate N availability reduce C allocation from the plant to the fungus and N allocation from the fungus to the plant (symbiotic resource exchange), (2) symbiotic resource exchange depends on relative N and P availability, and (3) fungal N translocation to plant and plant C allocation to fungus are interdependent. Birch (Betula pendula) seedlings were grown in symbiosis with the ectomycorrhizal fungus Paxillus involutus at five times excess N, or at five times excess N and P for 6 weeks. One-half of the plants were defoliated and the plant shoots were allowed to photosynthesize 14CO2 while the fungal compartment was exposed to 14NH4. After 3 days, the 14C of plant origin in fungal tissues and 15N of fungal origin in plant tissues were quantified. Nutrient availability had no observable effect on symbiotic resource exchange in non-defoliated systems. Defoliation reduced symbiotic N acquisition by plants at all levels of nutrient availability, with the reduction being most marked at higher N availability, indicating an increased tendency in the symbiotic system to discontinue resource exchange after defoliation at higher fertility levels. The concentration of 14C in extramatrical mycelium correlated significantly with the concentration of 15N in birch shoots. The results support the assumption that N delivery to the host by the mycorrhizal fungus is dependent on C flow from the plant to the fungus, and that exchanges between the partners are reciprocal. No significant reductions in root 14C content as a response to defoliation were observed, indicating that defoliation specifically reduced allocation to fungus, but not markedly to roots.

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Year:  2004        PMID: 15558328     DOI: 10.1007/s00572-004-0337-y

Source DB:  PubMed          Journal:  Mycorrhiza        ISSN: 0940-6360            Impact factor:   3.387


  8 in total

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Authors:  C A Gehring; T G Whitham
Journal:  Trends Ecol Evol       Date:  1994-07       Impact factor: 17.712

2.  Different photosynthesis-nitrogen relations in deciduous hardwood and evergreen coniferous tree species.

Authors:  P B Reich; M B Walters; B D Kloeppel; D S Ellsworth
Journal:  Oecologia       Date:  1995-09       Impact factor: 3.225

3.  Elevated CO2 and ozone reduce nitrogen acquisition by Pinus halepensis from its mycorrhizal symbiont.

Authors:  Minna-Maarit Kytöviita; Didier Le Thiec; Pierre Dizengremel
Journal:  Physiol Plant       Date:  2001-03       Impact factor: 4.500

4.  Microautoradiographic localization of phosphate and carbohydrates in mycorrhizal roots of Populus tremula x Populus alba and the implications for transfer processes in ectomycorrhizal associations.

Authors:  H Bücking; W Heyser
Journal:  Tree Physiol       Date:  2001-02       Impact factor: 4.196

5.  Defoliation effects on the ectomycorrhizal community of a mixed Pinus contorta/Picea engelmannii stand in Yellowstone Park.

Authors:  Kenneth W Cullings; Detlev R Vogler; V Thomas Parker; Shilpa Makhija
Journal:  Oecologia       Date:  2001-05-01       Impact factor: 3.225

6.  Extensive belowground carbon storage supports roots and mycorrhizae in regenerating scrub oaks.

Authors:  J Langley; B Drake; B Hungate
Journal:  Oecologia       Date:  2002-05-01       Impact factor: 3.225

7.  Effects of above-ground browsing by mammals on mycorrhizal infection in an early successional taiga ecosystem.

Authors:  L J Rossow; John P Bryant; Knut Kielland
Journal:  Oecologia       Date:  1997-03       Impact factor: 3.225

8.  Three-way interactions among ectomycorrhizal mutualists, scale insects, and resistant and susceptible pinyon pines.

Authors:  C A Gehring; N S Cobb; T G Whitham
Journal:  Am Nat       Date:  1997-05       Impact factor: 3.926

  8 in total
  4 in total

1.  Response of plants to ectomycorrhizae in N-limited conditions: which factors determine its variation?

Authors:  A Corrêa; R J Strasser; M A Martins-Loução
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2.  Carbon allocation in ectomycorrhizal plants at limited optimal N supply: an attempt aat unraveling conflicting theories.

Authors:  Ana Corrêa; Rüdiger Hampp; Elisabeth Magel; Maria-Amélia Martins-Loução
Journal:  Mycorrhiza       Date:  2011-01       Impact factor: 3.387

3.  Regulation of the leaf proteome by inoculation of Populus × canescens with two Paxillus involutus isolates differing in root colonization rates.

Authors:  Agnieszka Szuba; Łukasz Marczak; Leszek Karliński; Joanna Mucha; Dominik Tomaszewski
Journal:  Mycorrhiza       Date:  2019-08-27       Impact factor: 3.387

4.  Influence of leaf damage by the horse chestnut leafminer (Cameraria ohridella Deschka & Dimić) on mycorrhiza of Aesculus hippocastanum L.

Authors:  J Tyburska-Woś; K Nowak; B Kieliszewska-Rokicka
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  4 in total

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