The particularly high sensitivity to soil water deficit of leaf appearance on branches indicates that this process is a major determinant of the adaptation of plant leaf area to soil water deficit. The origin of this particular developmental response to soil water deficit is unclear, but it seems to be related to constitutive characteristics of branches rather than to competition for assimilates between axes differing in sink strength.

The application to grapevine of a generic model developed in annual plants made it possible to identify constants in main stem development and to determine the hierarchical structure of branches with respect to the modular structure of the stem in response to intra- and inter-shoot trophic competition.

BackgroundThe increasing temperature associated with climate change impacts grapevine phenology and development with critical effects on grape yield and composition. Plant breeding has the potential to deliver new cultivars with stable yield and quality under warmer climate conditions, but this requires the identification of stable genetic determinants. This study tested the potentialities of the microvine to boost genetics in grapevine. A mapping population of 129 microvines derived from Picovine x Ugni Blanc flb, was genotyped with the Illumina® 18 K SNP (Single Nucleotide Polymorphism) chip. Forty-three vegetative and reproductive traits were phenotyped outdoors over four cropping cycles, and a subset of 22 traits over two cropping cycles in growth rooms with two contrasted temperatures, in order to map stable QTLs (Quantitative Trait Loci).ResultsTen stable QTLs for berry development and quality or leaf area were identified on the parental maps. A new major QTL explaining up to 44 % of total variance of berry weight was identified on chromosome 7 in Ugni Blanc flb, and co-localized with QTLs for seed number (up to 76 % total variance), major berry acids at green lag phase (up to 35 %), and other yield components (up to 25 %). In addition, a minor QTL for leaf area was found on chromosome 4 of the same parent. In contrast, only minor QTLs for berry acidity and leaf area could be found as moderately stable in Picovine. None of the transporters recently identified as mutated in low acidity apples or Cucurbits were included in the several hundreds of candidate genes underlying the above berry QTLs, which could be reduced to a few dozen candidate genes when a priori pertinent biological functions and organ specific expression were considered.ConclusionsThis study combining the use of microvine and a high throughput genotyping technology was innovative for grapevine genetics. It allowed the identification of 10 stable QTLs, including the first berry acidity QTLs reported so far in a Vitis vinifera intra-specific cross. Robustness of a set of QTLs was assessed with respect to temperature variation.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-015-0588-0) contains supplementary material, which is available to authorized users.

Responses of grapevine vegetative growth components to mild, medium and severe soil water deficits were used to identify simple and sensitive indicators for early diagnosis of water stress. Soil water deficit was characterised as the fraction of transpirable soil water (FTSW) remaining in a water‐depleted rootzone. Growth components included the number of emerged leaves on first (Ist) and second (IInd) order lateral branches, the leaf area and internode length of each phytomer of Ist order lateral branches, and the frequency of IInd order lateral branching. These components were measured in a greenhouse on Shiraz (syn. Syrah) grapevines, over a 38‐day period of stabilised soil water regimes. Leaf emergence rate, final leaf area and final internode length of lateral branches I were relatively insensitive to mild and medium water deficits. They only decreased in response to severe water deficits. The frequency of IInd order lateral branching showed a similar trend, but was inhibited at severe water deficits. The leaf emergence rate of lateral branches II was highly sensitive to FTSW, and decreased even in response to mild water deficits. Because measurement of leaf emergence rate is a time consuming process, further analysis of the data was undertaken to identify a simpler but similarly effective indicator of cumulative water deficit. Accordingly, we established that the final length of lateral branches I was sensitive to medium water deficits, while the final ratio of the number of leaves on lateral branches II to the number of leaves on lateral branches I, was sensitive to even mild water deficits. Both of these composite indicators (derived variables) were relatively easy to measure and showed potential as early indicators of water deficits. They were more sensitive to FTSW than was predawn leaf water potential. Moreover, the final ratio of the number of leaves on lateral branches II to the number of leaves on lateral branches I was even more sensitive to FTSW than was stomatal conductance.