Echiniscus
publication ID |
https://doi.org/ 10.1111/zoj.12090 |
persistent identifier |
https://treatment.plazi.org/id/666D485F-FFB7-FFF6-FF5D-FA21FAC45956 |
treatment provided by |
Marcus |
scientific name |
Echiniscus |
status |
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RELATIONSHIPS WITHIN ECHINISCUS View in CoL
Deep phylogenetic structure within Echiniscus is missing for the most part, but a sister group relationship to D. oihonnae was well supported in all analyses. The majority of species or complexes of species (all but E. bigranulatus ) were supported but with different data sets: the blumi-canadensis complex, E. granulatus , E. spiniger , and E. testudo with 18S rRNA information ( Fig. 4A View Figure 4 ), and E. merokensis , E. wendti , E. spiniger , and E. testudo with 28S rRNA data ( Fig. 4B View Figure 4 ). Instead, the parsimony network constructed with the 18S rRNA data revealed three groups based on cuticular design that had statistical support (AMOVA: F ST = 0.944, P <0.001, genetic variation explained: 52.3% among cuticular design groups, 42.2% among populations within cuticular design groups, and 5.5% within populations). These three groups ( Fig. 5 View Figure 5 ) are composed of: (1) blumicanadensis ; (2) viridissimus , spiniger , testudo , bigranulatus , jenningsi , and wendti ; and (3) trisetosus Tar 612 and 635, granulatus and merokensis . By contrast, other classical groups based also on cuticle designs (presented in Table 1 and Fig. 1 View Figure 1 : bigranulatus , blumi-canadensis , merokensis , arctomys, and viridis ; Ramazzotti & Maucci, 1983; Peluffo et al., 2002; Pilato et al., 2007, 2008) did not find statistical or phylogenetic support from any of the genetic markers used, whether analysed individually or in combination. The parsimony network constructed with the 28S rRNA data or combining 18S and 28S rRNA sequences (networks not shown) did not yield any interpretable groups as specimens appeared mixed, and with no statistical (AMOVA) support (P> 0.05) in any case.
When considering uncorrected pairwise p -distances ( Table 5), differences within each Echiniscus species were up to 0.3% for 18S rRNA and up to 0.8% for 28S rRNA. Comparing uncorrected P -values among Echiniscus species , differences for 18S rRNA were 0.5–1.7% and for 28S rRNA 0.5–4.3%. Diploechiniscus oihonnae (sister group of Echinsicus ) had differences between 2.6 and 3.5% for 18S rRNA with respect to the Echiniscus species , and for 28S rRNA were 1.7–5.0%.
The sequence fragment delimited by primer pair 28Sa to 28S7b1 presented problems because the majority of the sequences were incomplete. A shorter fragment between primers 28Sa and 28S5b was complete in the majority of taxa and had enough differences to discriminate among species (a gap was present between within- and among-species differences; Table 5): within Echiniscus species genetic differences were 0.0–0.8%, and among Echiniscus species , 1.0–3.7%, this range being 2.4–4.1% for the sister group of Echiniscus , D. oihonnae , with respect to the Echiniscus species. In comparison, differences between Echiniscus species and Testechiniscus species were 1.8–4.1% for 18S rRNA and 2.8–4.5% for 28S rRNA fragment a-5b. Differences among other Heterotardigrada genera (from the same order) were 4.4–8.7% for 18S rRNA and 4.3–10.4% for 28S (a-5b) rRNA, and in Eutardigrada genera were 3.1–8.1% for 18S rRNA and 4.6–7.8% for 28S (a-5b) rRNA.
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