Monitoring CO 2 emissions to gain a dynamic view of carbon allocation to arbuscular mycorrhizal fungi

• Published in: Mycorrhiza Vol. 27; no. 1; p. 35
• Main Authors: Slavíková, Renata, Püschel, David, Janoušková, Martina, Hujslová, Martina, Konvalinková, Tereza, Gryndlerová, Hana, Gryndler, Milan, Weiser, Martin, Jansa, Jan
• Format: Journal Article
• Language: English
• Published: Germany 01-01-2017
• Subjects: Carbon - metabolism; Carbon Dioxide - chemistry; Carbon Dioxide - metabolism; Glomeromycota - physiology; Medicago truncatula - metabolism; Medicago truncatula - microbiology; Mycorrhizae - metabolism; Photosynthesis - physiology; Plant Roots - metabolism; Plant Shoots - metabolism; 13C isotope labelling; Medicago truncatula; Glomeromycota; Belowground carbon (C) allocation; Rhizophagus irregularis; Shade
• ISSN: 1432-1890

Quantification of carbon (C) fluxes in mycorrhizal plants is one of the important yet little explored tasks of mycorrhizal physiology and ecology.
CO
pulse-chase labelling experiments are increasingly being used to track the fate of C in these plant-microbial symbioses. Nevertheless, continuous monitoring of both the below- and aboveground CO
emissions remains a challenge, although it is necessary to establish the full C budget of mycorrhizal plants. Here, a novel CO
collection system is presented which allows assessment of gaseous CO
emissions (including isotopic composition of their C) from both belowground and shoot compartments. This system then is used to quantify the allocation of recently fixed C in mycorrhizal versus nonmycorrhizal Medicago truncatula plants with comparable biomass and mineral nutrition. Using this system, we confirmed substantially greater belowground C drain in mycorrhizal versus nonmycorrhizal plants, with the belowground CO
emissions showing large variation because of fluctuating environmental conditions in the glasshouse. Based on the assembled
C budget, the C allocation to the mycorrhizal fungus was between 2.3% (increased
C allocation to mycorrhizal substrate) and 2.9% (reduction of
C allocation to mycorrhizal shoots) of the plant gross photosynthetic production. Although the C allocation to shoot respiration (measured during one night only) did not differ between the mycorrhizal and nonmycorrhizal plants under our experimental conditions, it presented a substantial part (∼10%) of the plant C budget, comparable to the amount of CO
released belowground. These results advocate quantification of both above- and belowground CO
emissions in future studies.