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Members of Eupraxillella Hartmann-Schröder and Rosenlfelft, 1989, had been described with thirty chaetigers, 4 pre-pygidial achaetigers, a pygidium with a short edge, and with a ring of cirri anus on the cone, with anal ventral valve.

The form of the pygidium (with an anal pore found over the cone), and anal valve are normal for customers of Praxillella. The number of chaetigers among customers of Praxillella differs from 18 to 19, and there are 3‒4 pre-pygidial achaetigers. Based mostly primarily on the pygidium, situation of the anus and anal valve, Eupraxillella is a junior synonym of Praxillella , and Eupraxillella antarctica Hartmann-Schröder and Rosenlfelft, 1989, need to be regarded as Praxillella antarctica com.

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nov. Pseudoclyemene Arwidsson 1906 Arwidsson I. Studien über die Skandinavischen und Arktischen Maldaniden nebst zusammenstellung der brigen bisher bekannten Arten dieser Familie. Zool Jahr Supp 9: 1-308.

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was erected on the foundation of the duration of the nuchal grooves. This is a special character for the genus. Nevertheless, customers of this species have a pygidium with a limited edge, and a ring of cirri of distinct lengths the anus is found on the cone. Though Arwidsson (1906) Arwidsson I.

Studien über die Skandinavischen und Arktischen Maldaniden nebst zusammenstellung der brigen bisher bekannten Arten https://www.reddit.com/r/PaperHub/comments/x9r6o1/paper_help/ dieser Familie. Zool Jahr Supp 9: one-308.

does not explain the presence of an anal valve, the authentic figures resemble regular specimens of Praxillella . In this circumstance, we acknowledge Pseudoclyemene as a junior synonym of Praxillella , and P.

quadrilobata Arwidsson, 1906, will have to be regarded as Praxillella quadrilobata com. nov. Members of Euclymene africana ( Gravier ). From equally the text and figures, it is apparent that users of the species do not present a midventral cirrus that is more time than the remaining cirri, a problem that is component of the definition of Euclymene . As a result, these species are herein transferred to Isocirrus : I.

africana (Gravier, 1905) comb. nov. , and I.

watsoni (Gravier, 1905) comb. nov. Comments on monophyly of Euclymeninae: In their inferences of phylogenetic hypotheses describing morphological people between users of Maldanidae, De Assis and Christoffersen (2011) De Assis JE and Christoffersen ML. Phylogenetic interactions within just Maldanidae (Capitellida: Annelida), based on morphological people. Syst Biodiver 9: forty one-55. http://dx. doi. org/10.

https://doi. org/ten.

observed Euclymeninae to be monophyletic. Kobayashi et al. (2018) Kobayashi G, Goto R, Takano T and Kojima S. Molecular phylogeny of Maldanidae (Annelida): multiple losses of tube-capping plates and evolutionary shifts in habitat depth. Mol Phylogen Evol 127: 332-344. doi: https://doi. org/ten. ympev. 04. 036. https://doi. org/ten. ympev. 04. subsequently inferred phylogenetic hypotheses for only sequence details and obtained a paraphyletic Euclymeninae due to customers of Nicomachinae in just the former clade. Based mostly on their results, Kobayashi et al. (2018) Kobayashi G, Goto R, Takano T and Kojima S. Molecular phylogeny of Maldanidae (Annelida): many losses of tube-capping plates and evolutionary shifts in habitat depth. Mol Phylogen Evol 127: 332-344. doi: https://doi. org/10. ympev. 04. 036. https://doi. org/10. ympev. 04. concluded that the morphological people used by De Assis and Christoffersen (2011) De Assis JE and Christoffersen ML. Phylogenetic interactions inside of Maldanidae (Capitellida: Annelida), primarily based on morphological people. Syst Biodiver 9: 41-fifty five. http://dx. doi. org/ten. https://doi. org/ten. are not synapomorphies for Euclymeninae.

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