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Indicator genera analyses (999 permutations) based on sample groups predefined by treatment were carried out using the multipatt function of R to evaluate whether significant indicator genera were associated with pyrene treatment by calculating the group-equalized point-biserial correlation coefficient based on genera relative abundance data (Cáceres and Legendre 2009).
In the absence of fossil data for aloes and related genera, analyses were constrained to the mean age of 34.2 Ma inferred for the crown node of Asphodeloideae in a recent study of all Asparagales families [ 34].
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Pairwise comparison showed that this difference was significant in six of the ten genera analysed (one-way ANOVA; Table 2) and greatest in Glycine.
Total carotenoids contents was lower in the domesticated plants of the ten genera analysed (Table 2) whereby the extent of the difference with their wild progenitors was genus-dependent (P < 0.001, Figure 1A).
Molecular data do not support the distinction of Bangia and Porphyra as monophyletic genera, and analyses of these data have resulted in the transfer of a majority of species previously placed in Porphyra, including species of commercial value, to new genera (e.g. Nelson et al. 2006; Sutherland et al. 2011).
Twenty-one species from 21 gymnolaemate genera were analysed by immunocytochemical stainings and confocal laser scanning microscopy.
To distinguish between the genera of actinomycetes, analyses of the taxonomic and physicochemical properties of the organism are necessary, including analyses of mycolic acid and menaquinone and the sugars and amino acids composing the cell wall.
Several studies have shown that high level taxa can indeed be used as surrogates for species or genera in spatial analyses at the local or regional scale (e.g. [44] [45]; but see [46] for a different example).
Our results are in line with findings of previous studies [4] and a recent report that proposes a revision of the genus Microcoleus into at least two genera based on analyses of molecular, morphological, and structural characters [11].
For the purpose of assessing phylogenetic relationships, we choose representative species of the diplogastrid genera for molecular analyses.
It is likely that intrafamilial relationships can be further resolved by including other genera in rearrangement analyses.
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