Adropion, Pilato, 1987
publication ID |
https://doi.org/10.1093/zoolinnean/zlad151 |
publication LSID |
lsid:zoobank.org:pub:044A402-2A0F-4135-9410-7DE081CB11C4Corresponding |
DOI |
https://doi.org/10.5281/zenodo.14536918 |
persistent identifier |
https://treatment.plazi.org/id/03AF87C4-A632-FFB9-AC71-68DDFB248FA7 |
treatment provided by |
Plazi (2024-11-29 00:32:51, last updated 2024-12-20 16:23:39) |
scientific name |
Adropion |
status |
|
Composition of Adropion
The genus Adropion was inferred as polyphyletic by Bertolani et al. (2014). Gąsiorek and Michalczyk (2020) confirmed the non-monophyly of Adropion and established Guidettion (the latter having only three bar-like macroplacoids in the pharynx). However, the genus is still heterogeneous in terms of the number of macroplacoids: the majority of species exhibit three placoids, whereas there is a small group of species with only two macroplacoids, i.e. A. belgicae , A. diphasconiellum comb. nov. et stat. rev., and A. gani . The adoption of molecular phylogenetic methods in tardigrade research has shown that the number and shape of placoids in the pharynx is indicative of common ancestry (e.g. Gąsiorek et al. 2019, Guidetti et al. 2022). Thus, it is plausible that A. belgicae and A. diphasconiellum comb. nov. et stat. rev. are closely related and represent a separate evolutionary lineage. If reciprocal monophyly is confirmed molecularly, they should be erected as a new genus. However, A. gani is designated as nomen inquirendum, because having two rod-like macroplacoids arranged in parentheses (i.e. as in the members of the genus Pilatobius ) it does not fit the current diagnosis of Adropion . Moreover, recently three species of Adropion , each with three placoids, were transferred to Kararehius ( Zawierucha et al. 2023) . Their systematic affinity remains to be verified genetically.
Bertolani R, Guidetti R, Marchioro T et al. Phylogeny of Eutardigrada: new molecular data and their morphological support lead to the identification of new evolutionary lineages. Molecular Phylogenetics and Evolution 2014; 76: 110 - 26. https: // doi. org / 10.1016 / j. ympev. 2014.03.006
Gasiorek P, Stec D, Morek W et al. Deceptive conservatism of claws: distinct phyletic lineages concealed within Isohypsibioidea (Eutardigrada) revealed by molecular and morphological evidence. Contributions to Zoology 2019; 88: 78 - 132. https: // doi. org / 10.1163 / 18759866 - 20191350
Gasiorek P, Michalczyk L. Phylogeny of Itaquasconinae in the light of the evolution of the flexible pharyngeal tube in Tardigrada. Zoologica Scripta 2020; 49: 499 - 515. https: // doi. org / 10.1111 / zsc. 12424
Guidetti R, Giovannini I, Del Papa V et al. Phylogeny of the asexual lineage Murrayidae (Macrobiotoidea, Eutardigrada) with the description of Paramurrayon gen. nov. and Paramurrayon meieri sp. nov. Invertebrate Systematics 2022; 36: 1099 - 117. https: // doi. org / 10.1071 / IS 22031
Zawierucha K, Stec D, Dearden PK et al. Two new tardigrade genera from New Zealand's Southern Alp glaciers display morphological stasis and parallel evolution. Molecular Phylogenetics and Evolution 2023; 178: 107634. https: // doi. org / 10.1016 / j. ympev. 2022.107634
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
SubFamily |
Itaquasconinae |