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This suggests that plant species characteristic of each habitat are fairly evenly distributed on the shared species pool phylogeny, but that once the initial sorting of species into the two habitat types has occurred, the processes operating on them affect each habitat differently.
Both approaches yielded the same, highly resolved topology, which is largely congruent, for the shared species, with our current understanding of Saccharomycotina phylogeny [ 21].
This topology is congruent, for the shared species, with previous global fungal phylogenies (Fitzpatrick et al. 2006; Marcet-Houben and Gabaldón 2009) and with above results on noncoding RNA genes.
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The relative abundances of these shared species, however, shift from one site to another as shown in the previous section and below.
We used the abundance-based coverage estimator of species richness (ACE) and the Chao shared species estimator that provides a correction based on the relative abundance of rare species.
It is also possible that many of the apparently shared species may in fact be cryptic species or species that are distinguishable morphologically but lack apparent genetic differentiation.
Within the equation, c is the number of shared species and b is the number of species only in given GLT and not in ERG.
Each of the three sites shared species, particularly representatives of the genus Anthracobia.
In order to represent the number of shared species between each sample, the Sørensen Dice index was calculated for each pairwise comparison (Table 3).
Remember that the mean range size field is the proportion of shared species.
Nevertheless the number of shared species between MLS and LLS is also higher (11) than between ULS and MLS (9) (Table 2), which is consistent with BC clustering.
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