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However, in this case the wider thermal tolerance was interpreted to be the result of the changes in temperature experienced during the Pleistocene [ 50], while in the species of Troglocharinus the tolerance goes beyond the temperatures experienced through their entire evolutionary history.
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The trnN of L. pallens exhibited a mismatch in the sixth base pair of the acceptor stem, while in all of the species of Solenopsis, the TΨC stem was formed by only 2 bp and had a large TΨC loop.
The highest proportions of polymorphic SNPs were observed for E. grandis, E. urophylla and E. camaldulensis, between 40.9% and 49.4%, while in the two species of the more distant section Maidenaria, the proportion of polymorphic SNPs was around 22 to 25%.
Within the species of relevance (B. peninsularis and B. perkinsi), these pseudogenes were fixed at 100%% while prevalence of Wolbachia infections in other species was overly low (<20 %).
While we used in our studies in the majority species of the Agaricales and to less extend species from the Boletales and other orders (Table 2), Saar and colleagues analysed the electric properties of larger species ranges of Polyporales and Boletales with poroid hymenia, in addition to species from the Agaricales, Russulales and others (Saar 2013; Saar and Parmasto 2014; Saar and Salm 2014).
At a supraspecific level, the trio of C. spp. 17, 18 and 19 was found in the Neotropics, while the noncosmopolitan species of the sister group of C. elegans were all collected in Asia.
The bunyoro rabbit (Poelagus majorita) has a broad range in Central Africa, while the three species of rockhares (genus Pronolagus) are all found in Southern Africa.
Three previously proposed [ 46] active site residues, His190, Asp65, and Asp94 (E. coli numbering), are 100% conserved in the species studied, while replacement of His 247 with asparagine occurs in Caldivirga maquilingensis, Thermoplasma acidophilum, Picrophilus torridus, and Thermoplasma volcanium.
Species from outgroup families Propeamussiidae and Limidae are treated as byssal attachers: Waller [ 49] speculated that the typical habit of the Propeamussidae is to actively secrete a byssus based on the presence of a byssal notch in the adult, while species of the Limidae have been directly observed to byssally attach or build nests made of byssus threads [ 50, 51].
While in some species the location of the dnaA gene coincides with the origin of replication [ 29], this is not the case in H. influenzae and presumably not in A. actinomycetemcomitans either.
Thus, while the species in each of these assemblages are distributed across a range of body sizes, individuals are typically more similar in size and usually small.
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