Basic molecular phylogenetic information on the genus is available [ 3].
(C,D) Principal coordinate analysis of the UDCA and vitamin E treatment data at the genus level, respectively.
The analyses were generated from the abundance data at the genus level.
There is no reciprocal painting data on species of the genus Cebus.
Based on cytogenetic data, the genus Lepilemur can be divided into the eight traditionally recognized species, L. ankaranensis, L. dorsalis, L. edwardsi, L. leucopus, L. microdon, L. mustelinus, L. ruficaudatus and L. septentrionalis.
Available data on the vent mussel of genus Bathymodiolus are mainly focused on the effect of heavy metals and oxidative stress on enzymatic activities [ 14] and specific gene expression (e.g. metallothioneins) [ 15].
A previous study based on DNA sequence data has classified the genus into three subfamilies, Dryadoideae, Spiraeoideae, and Rosoideae, and each can be further separated into several supertribes and tribes.
More recently, in a phylogenetic analysis of the Infraorder Caridea based on 16S and 18S sequence data, the genus Lysmata formed a distinct clade, well separated from the other hippolytids [ 24], supporting Christoffersen's view of a paraphyletic Hippolytidae.
While several published papers confirm that lactobacilli are the dominant species in a healthy vaginal environment and are replaced by other commensal anaerobes (but remain present in very low numbers) in women with BV, there is a paucity of qPCR data on Lactobacillus genus and species in African populations.
These data confirmed the results of previous studies on the genus Quercus, highlighting the usefulness of this sequence for taxa identification [ 36].
The multivariate community data on genus level (standardised, square-root transformed, Bray-Curtis similarity was used to calculate resemblance) was analysed by means of non-parametric permutational ANOVA (PERMANOVA [45], [46]) to assess differences between the Gollum and Whittard areas, between water depths, and between sediment layers.
