Experimental evidence of two mechanisms coupling leaf-level C assimilation to rhizosphere CO 2 release

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Experimental evidence of two mechanisms coupling leaf-level C assimilation to rhizosphere CO 2 release. / Kayler, Zachary; Keitel, Claudia; Jansen, Kirstin et al.
in: Environmental and Experimental Botany, Jahrgang 135, 01.03.2017, S. 21-26.

Publikation: Beiträge in ZeitschriftenZeitschriftenaufsätzeForschungbegutachtet

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@article{cd523d0863214e5687a91b91d1348f65,
title = "Experimental evidence of two mechanisms coupling leaf-level C assimilation to rhizosphere CO 2 release",
abstract = "The time span needed for carbon fixed by plants to induce belowground responses of root and rhizosphere microbial metabolic processing is of high importance for quantifying the coupling between plant canopy physiology and soil biogeochemistry, but recent observations of a rapid link cannot be explained by new assimilate transport by phloem mass flow alone. We performed 13CO2 labeling experiments designed to test if belowground respiration response to photosynthesis is faster than the arrival of new assimilates and to shed light on potential mechanisms. We provide experimental evidence that at least two mechanisms are employed by plants to couple rhizosphere respiration to canopy assimilation. We observed a fast increase of belowground respiration with the onset of photosynthesis, which we assume is induced by pressure concentration waves travelling through the phloem. A second, much later occurring, peak in respiration is fueled by new assimilates labeled with 13C. Plants and the rhizosphere are thus more tightly coupled than previously thought. Ultimately, the addition of a faster assimilate delivery mechanism to our conceptual framework of ecosystem dynamics will lead to a better understanding of belowground carbon and nutrient cycling and subsequent ecosystem response to disturbance and environmental stress.",
keywords = "Biology, speed of link, phloem transport, soil respiration, pressure concentration wave, carbon isotope, rhizosphere",
author = "Zachary Kayler and Claudia Keitel and Kirstin Jansen and Arthur Gessler",
year = "2017",
month = mar,
day = "1",
doi = "10.1016/j.envexpbot.2016.12.002",
language = "English",
volume = "135",
pages = "21--26",
journal = "Environmental and Experimental Botany",
issn = "0098-8472",
publisher = "Elsevier B.V.",

}

RIS

TY - JOUR

T1 - Experimental evidence of two mechanisms coupling leaf-level C assimilation to rhizosphere CO 2 release

AU - Kayler, Zachary

AU - Keitel, Claudia

AU - Jansen, Kirstin

AU - Gessler, Arthur

PY - 2017/3/1

Y1 - 2017/3/1

N2 - The time span needed for carbon fixed by plants to induce belowground responses of root and rhizosphere microbial metabolic processing is of high importance for quantifying the coupling between plant canopy physiology and soil biogeochemistry, but recent observations of a rapid link cannot be explained by new assimilate transport by phloem mass flow alone. We performed 13CO2 labeling experiments designed to test if belowground respiration response to photosynthesis is faster than the arrival of new assimilates and to shed light on potential mechanisms. We provide experimental evidence that at least two mechanisms are employed by plants to couple rhizosphere respiration to canopy assimilation. We observed a fast increase of belowground respiration with the onset of photosynthesis, which we assume is induced by pressure concentration waves travelling through the phloem. A second, much later occurring, peak in respiration is fueled by new assimilates labeled with 13C. Plants and the rhizosphere are thus more tightly coupled than previously thought. Ultimately, the addition of a faster assimilate delivery mechanism to our conceptual framework of ecosystem dynamics will lead to a better understanding of belowground carbon and nutrient cycling and subsequent ecosystem response to disturbance and environmental stress.

AB - The time span needed for carbon fixed by plants to induce belowground responses of root and rhizosphere microbial metabolic processing is of high importance for quantifying the coupling between plant canopy physiology and soil biogeochemistry, but recent observations of a rapid link cannot be explained by new assimilate transport by phloem mass flow alone. We performed 13CO2 labeling experiments designed to test if belowground respiration response to photosynthesis is faster than the arrival of new assimilates and to shed light on potential mechanisms. We provide experimental evidence that at least two mechanisms are employed by plants to couple rhizosphere respiration to canopy assimilation. We observed a fast increase of belowground respiration with the onset of photosynthesis, which we assume is induced by pressure concentration waves travelling through the phloem. A second, much later occurring, peak in respiration is fueled by new assimilates labeled with 13C. Plants and the rhizosphere are thus more tightly coupled than previously thought. Ultimately, the addition of a faster assimilate delivery mechanism to our conceptual framework of ecosystem dynamics will lead to a better understanding of belowground carbon and nutrient cycling and subsequent ecosystem response to disturbance and environmental stress.

KW - Biology

KW - speed of link

KW - phloem transport

KW - soil respiration

KW - pressure concentration wave

KW - carbon isotope

KW - rhizosphere

U2 - 10.1016/j.envexpbot.2016.12.002

DO - 10.1016/j.envexpbot.2016.12.002

M3 - Journal articles

VL - 135

SP - 21

EP - 26

JO - Environmental and Experimental Botany

JF - Environmental and Experimental Botany

SN - 0098-8472

ER -

DOI