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Subsequently, we found that the wing patterns of 45 butterfly species closely related to genus Kallima were also composed of the NGP elements, although their appearances differed from the leaf-like patterns found in Kallima.
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The researchers determined that the wing patterns of, say, the map butterfly may be apparent to many birds, but to others of their kind their wing patterns are likely a blur, even from just a few inches away.
Because our comparative morphological analyses demonstrated that the wing patterns of species closely related to Kallima leaf butterflies are explained by the NGP, it is hypothesized that the developmental processes forming the wing patterns of these species include common molecular mechanisms, probably core developmental programs for wing pattern formation to satisfy the NGP.
We found that the wing margin phenotype characteristic of N 54/9/+ mutant wings (Fig. 2A) was strongly enhanced when dpn expression was reduced in the wing blade (Fig. 2D).
It was found that the wing shape used in this study resulted in the viscous features formed on the top of the wing exhibiting high sensitivity to the oscillating conditions and these influenced the performance of the wing.
The wing pattern of ismenias Meigen 1829.
Seasonal variation in the wing pattern of the Common Buckeye.
The analysis found that the pattern of missing records strongly matched the pattern of medallion taxi accidents across the city.
We find that the wing tissue shapes itself through patterned contractions and shear that occur in the context of patterned extra-cellular matrix (ECM) connections to a surrounding cuticular scaffold.
We found that the delorean wing phenotype is enhanced upon reduction of D-JNK when we observed the anterior wing margin of delorean homozygotes that carry one copy of the bsk allele (genotype: bsk pkn dln / pkn dln; Figure 5).
It was found that the reflectivity of black wings was lower than that of green wings, which was less than 8%% in the range of 400 900 nm.
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