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Studies by (Tsakalidou et al. 1994) have concluded that even though LAB are weakly lipolytic, the enterococcal strains showed a significantly higher activity than the strains of most other genera of LAB.
The blade narrows at one end instead of showing an expansion like most other genera.
Its location is variable, from a very anterior position in Rhinotermitinae, to a more posterior position in most other genera (see Table 1).
Considering that this genus contains by far the largest number of species of any genus in the family Aphididae, it is clear that Aphis has diversified to exploit an extremely large number of host plants [5], [6], but the morphologies of congeneric species are remarkably similar compared to those of most other genera [2], [5], [7], [8].
Among New World genera, we find Regina to be non-monophyletic with respect to most other genera, as in previous phylogenetic studies (e.g. [ 41, 186]).
Phenotypically similar LGT were common in all species of the genus, but also occurred in most other genera of the Helianthinae so far screened.
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In contrast, most other dinosaur genera are monospecific, containing only a single known species.
Most other related genera in Vitaceae, including Muscadinia, 2n = 40, have multiples of 10 chromosomes.
* p < 0.05; ** p < 0.01 Compared with other Cyperaceae and most other angiosperm genera, Eleocharis species vary greatly in genome size (Table 1[ 25]).
However, few sRNAs have been identified outside several well-studied species of gamma-proteobacteria and thus relatively little is known about the role of RNA-mediated regulation in most other bacterial genera.
In the course of the investigations on Orcula, samples of most other orculid genera (including Alvariella Hausdorf, 1996, Orculella Steenberg, 1925, Pilorcula Germain, 1912, Pagodulina Clessin, 1872, Sphyradium Charpentier, 1837 and Schileykula Gittenberger, 1983) were analyzed for the same set of mt and nc markers.
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