2011
DOI: 10.1111/j.1365-3040.2011.02328.x
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Genetic determinism of anatomical and hydraulic traits within an apple progeny

Abstract: The apple tree is known to have an isohydric behaviour, maintaining rather constant leaf water potential in soil with low water status and/or under high evaporative demand. However, little is known on the xylem water transport from roots to leaves from the two perspectives of efficiency and safety, and on its genetic variability. We analysed 16 traits related to hydraulic efficiency and safety, and anatomical traits in apple stems, and the relationships between them. Most variables were found heritable, and we… Show more

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Cited by 40 publications
(23 citation statements)
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“…This finding is consistent with the results of two recent surveys of cavitation resistance conducted on a Pinus species (Corcuera et al 2011, Lamy et al 2011. This finding is also Genotypic variability and phenotypic plasticity of cavitation 1179 consistent with the large genotypic variability found in apple progeny derived from the crossing of two varieties (Lauri et al 2011). By contrast, the genotypic variability between beech populations was remarkably small.…”
Section: Genotypic Variability Of Vulnerability To Cavitationsupporting
confidence: 91%
“…This finding is consistent with the results of two recent surveys of cavitation resistance conducted on a Pinus species (Corcuera et al 2011, Lamy et al 2011. This finding is also Genotypic variability and phenotypic plasticity of cavitation 1179 consistent with the large genotypic variability found in apple progeny derived from the crossing of two varieties (Lauri et al 2011). By contrast, the genotypic variability between beech populations was remarkably small.…”
Section: Genotypic Variability Of Vulnerability To Cavitationsupporting
confidence: 91%
“…; Lauri et al . ; Christensen‐Dalsgaard & Tyree ). Poplars and willows are both water‐demanding and drought‐sensitive genera (Cochard et al .…”
Section: Introductionmentioning
confidence: 99%
“…Also, a QTL on LG8 was found for BBI at both tree and axis scales in Durand et al (2013) and for BBI, yield and number of flowers per inflorescence in Guitton et al (2012). This zone, located at 8–23 cM on LG8, partially overlapped with QTLs detected in SG family for a descriptor of tree vegetation density (Virlet et al, 2015), for traits linked to bud break (Celton et al, 2011; Allard et al, 2016), and traits involved in gas exchange and xylem conductance (Segura et al, 2008; Regnard et al, 2009; Lauri et al, 2011). The QTL on LG10 located between 55 and 78 cM for BBIs, γ ax , θ g ,00 and θ g ,01 co-localized with those detected for BBI, precocity and number of seeds per inflorescence in SG (Guitton et al, 2012) and for the percentage of bourses with one fruit on short axes in XB family (Celton et al, 2014).…”
Section: Discussionmentioning
confidence: 83%