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(E) Flower of 35S::CsPI transgenic lines, the arrow labels the first floral organ; (F) Flower of 35S::CsPI transgenic lines, which have 5 petals and 5 petaloid sepals, the arrow labels the first floral organ; (G) Flower bud of the 35S::CsPI transgenic lines; (H) the margin epidermis of the first floral organ from 35S::CsPI transgenic lines.
(A) Wild Arabidopsis thaliana flower, the arrow labels the first floral organ; (B) Flower bud of the wild Arabidopsis thaliana; (C) Sepal epidermis of wild Arabidopsis thaliana flower; (D) Petal epidermis of wild Arabidopsis thaliana flower.
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The arrow labeled with Pb indicates the energy for backscattering from Pb atoms at the surface.
The arrow labeled "Trigger" indicates 14 46:40.2, when station OURI triggered the EEW procedure.
The arrow labeled Dedana F. at the top of the figure denotes the location of the surface trace of the Dedana fault.
The groundwater pressure sensor was replaced on October 8, 2014, after the 2014 eruption had started (indicated by the arrow labeled SC).
The arrow labeled "e" in Fig. 5c indicates air-fall ash deposits comprising fine ash particles aggregated with accretionary lapilli (Fig. 5e); the thickness of this layer was 2 3 mm, and the size of the particles was 1 2 mm.
As can be seen in Figure 5b, unlike the symmetrical phase transformation of Type II or III, the yielding of Type I is caused by a ZnO bond breaking, as shown by the arrow labeled 1.
Also, anomalous intensifications of the ionospheric density (determined from the fbEs) that exceeded the normal ambient background values for local time and location could be seen for a few days after the main phase of the magnetic storm (identified in the middle panel of Fig. 1 by the arrow labeled with the letters B and C).
In Figure 4, the time per step suddenly increases at step 46 as indicated by the arrow labelled A. This was caused by one of the nodes performing in a substandard way which resulted in the entire simulation to take twice as long, as the other nodes were waiting for this node to complete its share of the work.
The loop formed was T1S → T1R → T2S → T2R → T3S → T3R → T4S → T4R → T5S → T5R → T6S → T6R → T1S → T2S → T3S → T4S → T5S → T6S → T1S → T1R → T2R → T3R → T4R → T5R → T6R, where each arrow represents a separate hybridization (array) with the biological sample at the base of the arrow labeled with Cy3 and the biological pool at the head of the arrow labeled with Cy5.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com