Evidence map›Paper›PMID 25382456›Full record

ArticleThe New phytologist2015

Exploring the transfer of recent plant photosynthates to soil microbes: mycorrhizal pathway vs direct root exudation.

Christina Kaiser, Matt R Kilburn, Peta L Clode, Lucia Fuchslueger, Marianne Koranda, John B Cliff, Zakaria M Solaiman, Daniel V Murphy

Abstract read
In one paragraph

Article in The New phytologist, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

115 citing papers in PubMed.

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  20. Plant Diversity Reduces the Risk of Antibiotic Resistance Genes in Agroecosystems.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article

55 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Christina KaiserSoil Biology and Molecular Ecology Group, School of Earth and Environment, Institute of Agriculture, The University of Western Australia, Crawley, WA, 6009, Australia.
Matt R KilburnCentre for Microscopy, Characterisation and Analysis, The University of Western Australia, Crawley, WA, 6009, Australia.
Peta L ClodeCentre for Microscopy, Characterisation and Analysis, The University of Western Australia, Crawley, WA, 6009, Australia.
Lucia FuchsluegerDepartment of Microbiology and Ecosystem Science, Division of Terrestrial Ecosystem Research, Faculty of Life Sciences, University of Vienna, Althanstrasse 14, Vienna, A-1090, Austria.
Marianne KorandaDepartment of Microbiology and Ecosystem Science, Division of Terrestrial Ecosystem Research, Faculty of Life Sciences, University of Vienna, Althanstrasse 14, Vienna, A-1090, Austria.
John B CliffCentre for Microscopy, Characterisation and Analysis, The University of Western Australia, Crawley, WA, 6009, Australia.
Zakaria M SolaimanSoil Biology and Molecular Ecology Group, School of Earth and Environment, Institute of Agriculture, The University of Western Australia, Crawley, WA, 6009, Australia.
Daniel V MurphySoil Biology and Molecular Ecology Group, School of Earth and Environment, Institute of Agriculture, The University of Western Australia, Crawley, WA, 6009, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plants rapidly release photoassimilated carbon (C) to the soil via direct root exudation and associated mycorrhizal fungi, with both pathways promoting plant nutrient availability. This study aimed to explore these pathways from the root's vascular bundle to soil microbial communities. Using nanoscale secondary ion mass spectrometry (NanoSIMS) imaging and (13) C-phospho- and neutral lipid fatty acids, we traced in-situ flows of recently photoassimilated C of (13) CO2 -exposed wheat (Triticum aestivum) through arbuscular mycorrhiza (AM) into root- and hyphae-associated soil microbial communities. Intraradical hyphae of AM fungi were significantly (13) C-enriched compared to other root-cortex areas after 8 h of labelling. Immature fine root areas close to the root tip, where AM features were absent, showed signs of passive C loss and co-location of photoassimilates with nitrogen taken up from the soil solution. A significant and exclusively fresh proportion of (13) C-photosynthates was delivered through the AM pathway and was utilised by different microbial groups compared to C directly released by roots. Our results indicate that a major release of recent photosynthates into soil leave plant roots via AM intraradical hyphae already upstream of passive root exudations. AM fungi may act as a rapid hub for translocating fresh plant C to soil microbes.

Indexed as

PhotosynthesisSoil MicrobiologyBiomarkersCarbonCarbon IsotopesColony Count, MicrobialFatty AcidsHyphaeLightMycorrhizaeNanotechnologyNitrogenNitrogen IsotopesPhospholipidsPlant ExudatesPlant RootsBiomarkersCarbonCarbon IsotopesFatty AcidsNitrogenNitrogen IsotopesPhospholipidsPlant Exudatesarbuscular mycorrhizal (AM) fungibelowground carbon allocationhyphospheremycorrhizosphereNanoSIMSpriming effectrecent photosynthatesroot exudates

Identifiers

PMID25382456
PMCPMC4357392

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.