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Because genetic diversity (Fig. 1b) was sampled independently of the other population characteristics i.e. at slightly different sites (Fig. 1c-e), genetic diversity was attributed to each exact kelp forest using its strong relationship with latitude (Table S2).
This morphology diversity was attributed to the radial variation of parameters including temperature, viscosity, axial velocity and stress in spinning path and was in good agreement with the droplet deformation criteria based on the reduced capillary number.
An important bulk of species diversity was attributed to the prokaryotic (Bacteria and Archaea) and eukaryotic (Protists) marine microbes.
In this case, high diversity was attributed to the area serving as a glacial refugium and for maintaining a very large population size in a favorable climate.
The AMOVA results also showed that most of the genetic diversity was attributed to the among-population effects.
However, when looking at how diversity is partitioned among groups via AMOVA, we noticed that most of the diversity was attributed to differences within groups (88.1%, against 62.5% on Garris' report), rather than among the three inferred groups.
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These high measures of population-level diversity were attributed to long lifespan and wind-mediated pollen dispersal.
Responsibility for the low diversity is attributed to the highly frequent E3a*-M2 and E1*-M33 lineages (72.0% and 15.6%, respectively) that are shared among all ethnic clusters.
Nearly 10% of all angiosperms are contained within the Asterales; a clade that is mainly comprised of 12 recognized families with a majority of the diversity being attributed to just two families, Asteraceae (e.g. sunflowers, thistles) and Campanulaceae (e.g. Lobelia and relatives).
The viral load within the surface microlayer of scleractinian corals is enumerated as being 10-10 VLPs mL-1[ 379] and, based on VLP morphological diversity, is attributed to infecting various microbial hosts (bacteria, archaea, cyanobacteria, fungi and algae) residing within the coral mucus [ 380].
Mutation rates were shown to be similar in humans and Drosophila [ 39, 40], so the ten fold difference in average nucleotide diversity between species was attributed to the approximately ten fold larger long term effective population size in Drosophila than in humans (Ne = 300,000 versus 20,000 respectively) [ 41, 42].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com