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Many systematists have given special emphasis to morphological similarities shared between aphelenchs and tylenchs, as discerned by light microscopy, such as the protrusible stomatostylet, esophageal structures, and genital structure in females [ 15, 16, 18, 49- 53].
The morphological support for such hypotheses is weak, however, and the best evolutionary explanation for the detailed morphological similarities shared by afrotherian paenungulates and laurasiatherian ferungulates remains convergent acquisition in isolation, rather than in sympatry [ 19].
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This association is also supported by morphological similarities in euspermatozoa shared by many members of this clade [ 38].
Thus, genetic similarity, shared morphological traits, and their sympatric distributions further support the hypothesis of a hybridization event between the species related to X. maculatus and X. mixei.
The H. sapiens scaphoid morphology shares morphological similarities with both Au.
Although the overall landscape of trait variations was not structured, it remained possible that some subgroups of strains shared morphological similarities.
Hong [ 19] speculated that Pterygiella Oliver and Xizangia D.Y. Hong, two genera of the traditional tribe Rhinantheae endemic to China, shared morphological similarities with Pedicularis and Phtheirospermum Bunge ex Fischer & C.A. Meyer.
MVHPs exhibit morphological similarities with SSA/P, share high frequency of BRAF mutations and are commonly detected in the distal colon.
However, little information is available on the brain response to implanted high-aspect-ratio nanoparticles, which share morphological similarities with asbestos fibres.
Each cell has distinct gene-expression patterns even when sharing morphological similarities.
Moreover, although M. catarrhalis is focused on by clinicians, the isolation of M. catarrhalis from clinical samples is complicated by the presence of Neisseria strains because these organisms share morphological similarities [ 49].
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