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In this context, our study, motivated by such inconsistency between molecular and morphological data, provides valuable information that could help to distinguish the relevant factors involved in morphological variation of male genitalia in D. buzzatii and D. koepferae, a pair of species in the heart of an evolutionary conflict.
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However, the precise systematic position of Bourreria within Ehretiaceae cannot be resolved on the basis of the morphological data provided here.
Together, these morphological data provide additional evidence that GFP+ cells are newborn neurons and that many of them have reached advanced stages of development [7], [20], [46]-[48].
We report high levels of variation in the PEPCK gene fragment, and although the mixed model did not provide a better fit than a null coalescent, using both markers in combination with morphological data provided resolution for many species of Rhithrogena and constitutes an important advance in our understanding of this morphologically cryptic group.
Both molecular and morphological data provide strong support for considering the "Long-billed" Vulture to be comprised of two species (G. indicus and G. tenuirostris), and further analysis is warranted to determine the taxonomic distinctiveness of G. f. fulvescens.
Both molecular and morphological data provide strong support for considering the "Long-billed" Vulture (G. indicus) to be comprised of two species, the Long-billed Vulture (G. indicus) and the Slender-billed Vulture (G. tenuirostris), with both considered critically endangered by the IUCN [ 1].
As a basal step in deciphering peptidergic circuits, the data provides a morphological rationale to help identify candidate pre- and postsynaptic neurons by analysis of overlapping projections.
Recent cladistic analyses of morphological data have provided an undeniable advance in identifying the closest relatives of the theridiids as well as establishing the family's monophyly.
Our aim was to examine whether the combination of extensive morphological data could provide information to infer their likely relationships.
Morphological data are provided as supplementary information in Additional file 3. Additional file 1: A summary of the proteomics data analysis from Progenesis QI with abundances normalized using all 383 proteins.
This data provides an additional line of evidence supporting the genetic and morphological data that the SABD is distinct from the CBD in Victorian waters, Australia.
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