2019
DOI: 10.1093/treephys/tpy131
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Plant-PET to investigate phloem vulnerability to drought inPopulus tremulaunder changing climate regimes

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Cited by 16 publications
(27 citation statements)
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“…The indirect empirical evidence of phloem transport failure comes from detection of severe shrinkage of phloem tissue prior to mortality , indirect measurement of phloem turgor loss (Salmon et al unpublished data), lack of labelled carbohydrate detection in phloem sap and stem respiration after pulse labelling with either 13 C (Dannoura et al 2019) or 11 C (Hubeau et al 2019), total depletion of carbohydrates in the roots of Norway spruce, while the canopy does not suffer reserve depletion (Hartmann et al 2013b).…”
Section: Is the Phloem Involved In Drought-induced Mortality?mentioning
confidence: 99%
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“…The indirect empirical evidence of phloem transport failure comes from detection of severe shrinkage of phloem tissue prior to mortality , indirect measurement of phloem turgor loss (Salmon et al unpublished data), lack of labelled carbohydrate detection in phloem sap and stem respiration after pulse labelling with either 13 C (Dannoura et al 2019) or 11 C (Hubeau et al 2019), total depletion of carbohydrates in the roots of Norway spruce, while the canopy does not suffer reserve depletion (Hartmann et al 2013b).…”
Section: Is the Phloem Involved In Drought-induced Mortality?mentioning
confidence: 99%
“…Similarly, even if evidence of reduced carbohydrate pools e.g. in root tissue indicate slow or no phloem transport (Hartmann et al 2013a;Hartmann et al 2013b), more direct measurements based on the detection of labelled carbohydrates (Dannoura et al 2019;Hubeau et al 2019) are needed to confirm cessation of transport in a wider range of tree species, and the possible reasons for it. Intriguingly, in at least some species the effect of carbohydrate reserves on plant survival time (O'Brien et al 2014) could arise from varying access to reserves or varying phloem transport capacity among plants in the same environment ).…”
Section: Is the Phloem Involved In Drought-induced Mortality?mentioning
confidence: 99%
“…Woody tissue photosynthetic rates range between 0.5 and 9 μmol CO 2 m −2 s −1 , with median values of 1.9 μmol CO 2 m −2 s −1 , and are generally lower than those in leaves, with maximum values being up to 75% of leaf photosynthesis (Ávila et al, ; Pfanz et al, ). Nevertheless, P wt is an important local carbon source for plant functioning, especially during drought stress when leaf photosynthesis and phloem transport are limited following stomatal closure and phloem dysfunction, respectively (Cernusak & Cheesman, ; Hubeau et al, ; Steppe, Sterck, & Deslauriers, ; Vandegehuchte et al, ).…”
Section: Introductionmentioning
confidence: 99%
“…The potential of 11 C-positron emission tomography ( 11 C-PET) in plant studies remains largely untapped (Hubeau and Steppe, 2015). In past studies, 11 C-tracing has been used to study the transport speed of phytomolecules such as plant hormones (e.g., methyl jasmonate in Thorpe et al, 2007) and photoassimilates (Kikuchi et al, 2008), and 11 C-imaging has been used to visualize the phloem pathway for part of the plant (Kawachi et al, 2006;Jahnke et al, 2009;De Schepper et al, 2013;Hubeau et al, 2019a) or the entire plant (Kawachi et al, 2011). The acquired tracer profiles can be implemented in mathematical models to study sugar loading, sugar translocation, radial sugar leakage and sugar unloading (Bühler et al, 2011(Bühler et al, , 2014Minchin, 2012;Hubeau et al, 2019a).…”
Section: The Power Of Imaging 11 C-labeled Compounds In Plant Researchmentioning
confidence: 99%
“…Also, the 20 min halflife of 11 C limits its use to short-term processes, in contrast to the longer-lived carbon isotope 14 C (half-life of 5,730 years). On the positive side, 11 C-tracing allows an in vivo observation of tracer movement, which has led to significant research progress in topics such as phloem sectoriality (De Schepper et al, 2013), unloading characteristics (Jahnke et al, 2009), leakage-retrieval of photoassimilates along the transport pathway (Thorpe and Minchin, 1991), phloem functioning under changing climate regimes (Hubeau et al, 2019a) and carbon allocation to root and fruit parts (Jahnke et al, 2009;Wang et al, 2014). Importantly, non-invasive measurements allow dynamic aspects of a process to be studied, and 11 C therefore provides a powerful tool to reveal the mechanisms of physiological processes (Minchin and Thorpe, 2003;Jahnke et al, 2009;Bühler et al, 2011;Hubeau et al, 2019a).…”
Section: Introductionmentioning
confidence: 99%