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We then used 2000 complete millet seeds from NKLE-F4T3P7L57F1 for microscopy observation and morphological analysis of the angle of the embryo notch, width of the opening of the embryo notch, and depth of the embryo notch.
We measured several parameters: (1) angle of the embryo notch, θ; (2) width of the opening of the embryo notch, w1; (3) total width of the seed, wt; (4) depth of the embryo notch, d1; and (5) depth of the seed at the longest side, dt (Fig. 2b).
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We found that the required pulse energy increases as a function of depth within the embryo, as shown in Fig. 3(A).
A final prediction of our model is that a reversal of embryonic elongation should lead to a consequent reduction in the depth of the keyhole in embryos.
In addition, the average depth of the keyhole in these embryos was typically greater than that observed for mec-8; sym-3 or mec-8; sym-4 mutants as well as for fbn-1 single mutants (Table 1).
We then measured the angle, depth percentage and width percentage of the embryo notch for both modern and ancient millet seeds (Table 1).
The depth of the magma ocean is dependent on the time between the embryo-embryo collision and the planetesimal impact as well as the cooling rate of the magma ocean (Fig. 4, points contained in the black ellipse).
To investigate how predictions would improve with the availability of grandparental genotypes, we sequenced the genomes of the embryo's four grandparents to 10× depth.
Depending on the gestational age of the embryo, regions-of-interest in the image can extend well beyond the depth-of-focus for a fixed-focus transducer.
θ angle of embryo notch; w 1 width of the opening of the embryo notch; w t width of the seed at the longest side; d 1 depth of embryo notch; d t depth of the seed at the longest side.
Would you like to know the sex of the embryo?
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