Literature DB >> 28307122

Leaf 15N abundance of subarctic plants provides field evidence that ericoid, ectomycorrhizal and non-and arbuscular mycorrhizal species access different sources of soil nitrogen.

Anders Michelsen1,2, Inger K Schmidt1, Sven Jonasson1, Chris Quarmby2, Darren Sleep2.   

Abstract

The natural abundance of the nitrogen isotope 15, δ15N, was analysed in leaves of 23 subarctic vascular plant species and two lichens from a tree-line heath at 450 m altitude and a fellfield at 1150 m altitude close to Abisko in N. Sweden, as well as in soil, rain and snow. The aim was to reveal if plant species with different types of mycorrhizal fungi also differ in their use of the various soil N sources. The dwarf shrubs and the shrubs, which in combination formed more than 65% of the total above-ground biomass at both sites, were colonized by ericoid or ectomycorrhizal fungi. Their leaf δ15N was between-8.8 and-5.5‰ at the heath and between-6.1 and -3.3‰ at the fellfield. The leaf δ15N of non- or arbuscular mycorrhizal species was markedly different, ranging from -4.1 to -0.4‰ at the heath, and from -3.4 to+2.2‰ at the fellfield. We conclude that ericoid and ectomycorrhizal dwarf shrubs and shrubs utilize a distinct N source, most likely a fraction of the organic N in fresh litter, and not complexed N in recalcitrant organic matter. The latter is the largest component of soil total N, which had a δ15N of -0.7‰ at the heath and +0.5‰ at the fellfield. Our field-based data thus support earlier controlled-environment studies and studies on the N uptake of excised roots, which have demonstrated protease activity and amino acid uptake by ericoid and ectomycorrhizal tundra species. The leaves of ectomycorrhizal plants had slightly higher δ15N (fellfield) and N concentration than leaves of the ericoids, and Betula nana, Dryas octopetala and Salix spp. also showed NO inf3sup- reductase activity. These species may depend more on soil inorganic N than the ericoids. The δ15N of non- or arbuscular mycorrhizal species indicates that the δ15N of inorganic N available to these plants was higher than that of average fresh litter, probably due to high microbial immobilization of inorganic N. The δ15N of NH inf4sup+ -N was +12.3‰ in winter snow and +1.9‰ in summer rain. Precipitation N might be a major contributer in species with poorly developed root systems, e.g. Lycopodium selago. Our results show that coexisting plant species under severe nutrient limitation may tap several different N sources: NH inf4sup+ , NO inf3sup- and organic N from the soil, atmospheric N2, and N in precipitation. Ericoid and ectomycorrhizal fungi are of major importance for plant N uptake in tundra ecosystems, and mycorrhizal fungi probably exert a major control on plant δ15N in organic soils.

Entities:  

Keywords:  Arctic mycorrhiza; Legume and lichen N2 fixation; Nitrate reductase activity; Plant; Stable isotopes; soil and precipitation δ15N

Year:  1996        PMID: 28307122     DOI: 10.1007/BF00328791

Source DB:  PubMed          Journal:  Oecologia        ISSN: 0029-8549            Impact factor:   3.225


  8 in total

1.  In situ mineralization of nitorgen and phosphorus of arctic soils after perturbations simulating climate change.

Authors:  Sven Jonasson; Mats Havström; Michael Jensen; Terry V Callaghan
Journal:  Oecologia       Date:  1993-08       Impact factor: 3.225

2.  Estimation of N2 fixation based on differences in the natural abundance of 15N among freshwater N2-fixing and non-N2-fixing algae.

Authors:  B Gu; V Alexander
Journal:  Oecologia       Date:  1993-10       Impact factor: 3.225

3.  The ability of several high arctic plant species to utilize nitrate nitrogen under field conditions.

Authors:  Owen K Atkin; Rafael Villar; W Raymond Cummins
Journal:  Oecologia       Date:  1993-11       Impact factor: 3.225

4.  The nutritional status of plants from high altitudes : A worldwide comparison.

Authors:  Ch Körner
Journal:  Oecologia       Date:  1989-11       Impact factor: 3.225

5.  Nitrogen nutrition and isotope differences among life forms at the northern treeline of Alaska.

Authors:  E-D Schulze; F S Chapin; G Gebauer
Journal:  Oecologia       Date:  1994-12       Impact factor: 3.225

6.  Natural 15N abundance of presumed N2-fixing and non-N2-fixing plants from selected ecosystems.

Authors:  Ross A Virginia; C C Delwiche
Journal:  Oecologia       Date:  1982-09       Impact factor: 3.225

7.  Shoot biomass, δ13C, nitrogen and chlorophyll responses of two arctic dwarf shrubs to in situ shading, nutrient application and warming simulating climatic change.

Authors:  Anders Michelsen; Sven Jonasson; Darren Sleep; Mats Havström; Terry V Callaghan
Journal:  Oecologia       Date:  1996-01       Impact factor: 3.225

8.  Inhibition of growth, and effects on nutrient uptake of arctic graminoids by leaf extracts - allelopathy or resource competition between plants and microbes?

Authors:  Anders Michelsen; Inger K Schmidt; Sven Jonasson; John Dighton; Helen E Jones; Terry V Callaghan
Journal:  Oecologia       Date:  1995-09       Impact factor: 3.225

  8 in total
  22 in total

1.  Weak habitat specificity in ectomycorrhizal communities associated with Salix herbacea and Salix polaris in alpine tundra.

Authors:  Martin Ryberg; Mathias Andreasen; Robert G Björk
Journal:  Mycorrhiza       Date:  2010-08-03       Impact factor: 3.387

2.  Foliar pH as a new plant trait: can it explain variation in foliar chemistry and carbon cycling processes among subarctic plant species and types?

Authors:  J H C Cornelissen; H M Quested; R S P van Logtestijn; N Pérez-Harguindeguy; D Gwynn-Jones; S Díaz; T V Callaghan; M C Press; R Aerts
Journal:  Oecologia       Date:  2005-10-11       Impact factor: 3.225

3.  Does warming by open-top chambers induce change in the root-associated fungal community of the arctic dwarf shrub Cassiope tetragona (Ericaceae)?

Authors:  Kelsey Erin Lorberau; Synnøve Smebye Botnen; Sunil Mundra; Anders Bjørnsgaard Aas; Jelte Rozema; Pernille Bronken Eidesen; Håvard Kauserud
Journal:  Mycorrhiza       Date:  2017-03-27       Impact factor: 3.387

4.  Foliar and fungal 15N:14N ratios reflect development of mycorrhizae and nitrogen supply during primary succession: testing analytical models.

Authors:  Erik A Hobbie; Ari Jumpponen; Jim Trappe
Journal:  Oecologia       Date:  2005-10-28       Impact factor: 3.225

5.  Characteristics of root-cultivable endophytic fungi from Rhododendron ovatum Planch.

Authors:  Lei-Chen Lin; Yu-Sin Ye; Wan-Rou Lin
Journal:  Braz J Microbiol       Date:  2018-12-03       Impact factor: 2.476

6.  Foliar 15N natural abundance indicates phosphorus limitation of bog species.

Authors:  Beverley R Clarkson; Louis A Schipper; Bernard Moyersoen; Warwick B Silvester
Journal:  Oecologia       Date:  2005-05-11       Impact factor: 3.225

7.  Microbial biomass C, N and P in two arctic soils and responses to addition of NPK fertilizer and sugar: implications for plant nutrient uptake.

Authors:  Sven Jonasson; Anders Michelsen; Inger K Schmidt; Esben V Nielsen; Terry V Callaghan
Journal:  Oecologia       Date:  1996-06       Impact factor: 3.225

8.  15N natural abundances and N use by tundra plants.

Authors:  K Nadelhoffer; G Shaver; B Fry; A Giblin; L Johnson; R McKane
Journal:  Oecologia       Date:  1996-08       Impact factor: 3.225

9.  The natural abundance of (15)N in mat-forming lichens.

Authors:  Christopher J Ellis; Peter D Crittenden; Charles M Scrimgeour; Carl Ashcroft
Journal:  Oecologia       Date:  2003-04-15       Impact factor: 3.225

10.  Combustion influences on natural abundance nitrogen isotope ratio in soil and plants following a wildfire in a sub-alpine ecosystem.

Authors:  Edith Huber; Tina L Bell; Mark A Adams
Journal:  Oecologia       Date:  2013-05-07       Impact factor: 3.225

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