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Tiphallus torreon n. sp., the fi rst rhachodesmid milliped from Coahuila, Mexico, displays an iridescent turquoise pigmentation with patterned white paranotal markings and a truncated, subapical projection from the broad, non-descript gonopodal acropodite. Four genera – Strongylodesmus Saussure, Mexidesmus Loomis, and Ceuthauxus and Tiphallus, both by Chamberlin – contain forms exhibiting this general condition, but the last is the only one whose type species does. Synthetic treatments are essential to advance familial knowledge beyond the descriptive stage, and revising these four taxa would constitute a meaningful initial study. Rhachodesmidae extend from northern Nuevo León, Mexico, ca. 77 km (48 mi) from the Rio Grande, to central Costa Rica; Glomeridae (Glomerida), Platydesmidae (Platydesmida), and Stemmiulidae (Stemmiulida) show similar distributions whereas Allopocockiidae (Spirobolida) and Rhysodesmus Cook (Polydesmida: Xystodesmidae) traverse the river and occupy southernmost Texas. Tridontomidae, the other component of Rhachodesmoidea, occupies a small enclave in Alta Verapaz, Guatemala. Rhachodesmidae/oidea do not occur in Panama and are initially recorded from Belize; localities are needed from Honduras.
Mimuloria Chamberlin 1928 is revived from synonymy under Nannaria Chamberlin 1918a for Nannariini (Polydesmida: Xystodesmidae) with simple but apically ornamented gonopodal acropodites that arch or lean mediad and cross body midlines and opposing acropodites in situ. It encompasses two assemblages based primarily on the nature of the ornamentations, the castanea and dilatata species groups. The former includes three established species [M. castanea (McNeill 1887) M. missouriensis Chamberlin 1928 and M. davidcauseyi (Causey 1950a)], and the latter contains two new ones (M. dilatata [M. d. dilatata, M. d. sigmoidea], and M.
rhysodesmoides). Castanaria Causey 1950b is returned to synonymy under Mimuloria, and C. depalmai Causey 1950b is placed under M. castanea, thereby constituting a new synonymy. The fi rst illustrations of the holotype gonopods of Fontaria oblonga C. L. Koch 1847 and N. minor Chamberlin 1918a unequivocally establish their identities, and the convoluted nomenclatural tangle involving Oenomaea Hoffman 1964 and O. pulchella (Bollman 1889a) is detailed. Whether in Oenomaea or a new genus, separate generic status seems appropriate for Nannariini with subterminal solenomeres; N. morrisoni Hoffman 1948 and its potential synonym N. shenandoa Hoffman 1949 may also belong here. Initial tribal localities are reported from Alabama, South Carolina, and coastal Virginia and Maryland, and “O. pulchella” occurs in northern Alabama north/west of the Tennessee River; M. castanea is newly recorded from Missouri and Tennessee. A horizontally subtriangular distribution in the eastern and midwestern states is projected for Nannariini, which even occur on South Bass Island, Ohio, in Lake Erie, and may thus inhabit
nearby Pelee Island, Ontario, Canada.