Sentence examples for shoot leaf from inspiring English sources

The major explanatory variable highlighted in these experiments was the shoot leaf number, mainly early in the season.

Anatomical meta-expression data reveal that Lsi6 is highly expressed in the root, shoot, leaf, and palea/lemma tissues.

Application of GB to plants grown in a controlled environment slightly reduced growth rates, resulting in a lower shoot leaf area at concentrations of 50, 100, or 200 mM.

At the end of the four-week recovery period, new shoot, leaf, rhizome, shootbase, total biomass, and RGR were lower in the 137-cm depth treatment than in both the 40- and 91-cm depth treatments, but there were no differences for these variables between the 40- and 91-cm depth treatments.

Additionally, transcriptome resources were generated from various tissues including xylem, phloem, root, shoot, leaf and reproductive tissues from species such as E. grandis, E. gunnii, E. globulus, E. camaldulensis and E. tereticornis (Mizrachi et al. [2010]; http://web.up.ac.za/eucagen/; http://eucgenie.org/; Healey et al. [2014]).

The latter two genes were expressed in shoot, leaf and culm in moderately high levels.

Number of leaf shoots, leaf heights and surface water depth (<30 cm and >60 cm) were recorded for each quadrat.

Tissue samples were taken at 40 DAS; shoots (leaf blade) and roots were rapidly frozen in liquid nitrogen and stored at −70°C until analyzed.

In class IV shoots, leaf outgrowth was suppressed, and gametophores comprised a raspberry-like dome of cells above a zone of rhizoid emergence.

Expression of SNB and Os03g60430 showed an inverse correlation with the abundance of miR172 in two-leaf shoots, leaf four and leaf ten, but generally the expression of miR172 was not inversely correlated with the expression of its targets in the tissues analyzed.

Tissue samples of tender shoot, young leaf, expanded leaf, mature leaf, flower, and fruit were collected in 2010.