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With the discovery of Mitocybe auriportae Cook and Loomis, 1928 (Platydesmida: Andrognathidae) in Alameda County (Co.), east of San Francisco Bay, a potential overall distribution in coastal California is projected based on those of partly congruent diplopods. The area extends from northern Mendocino to central Monterey cos. and inland to central Lake, Yolo, and Santa Clara cos.
Past concepts and synonymies of Anadenobolus monilicornis (Porat, 1876) (Spirobolida: Rhinocricidae), including the implied synonymy of Rhinocricus ectus Chamberlin, 1920, are consolidated into a formal account with the fi rst illustrations of the holotype. Prior to 1492, A. monilicornis was probably indigenous to an unknown number of southern Antillean islands, but through modern commerce, man has introduced it to Florida, Bermuda, Barbados, the Cayman Islands, and Jamaica, and probably repeatedly (re)introduced conspecifi c material to all the Lesser Antilles, resulting in subcontinuous gene pool mixing and reticulate evolution. A broad species concept is necessary to encompass the multitudinous variants, some of which have been recognized as species; only one true Caribbean species of Anadenobolus Silvestri, 1897, may exist, for which arboreus (Saussure, 1859) is the oldest name. The distribution of A. monilicornis presently extends from Bermuda and southern coastal Florida through the Greater and Lesser Antilles (excepting Cuba) to eastern coastal Venezuela and central Suriname, with outlier populations in Jamaica, the Cayman Islands, and Tampa Bay and the eastern Floridian panhandle; excepting Barbados, the indigenous range may have extended from Hispaniola through the same area. Introductions into Manitoba, Canada, and North Carolina, USA, have not yielded viable populations. Localities are newly recorded from St. Thomas, US Virgin Islands.
A summary of the milliped faunas of Pakistan, Bangladesh, and Kashmir (Arthropoda: Diplopoda)
(2014)
Three female callipodidan samples from northern Pakistan are assigned to Bollmania kohalana (Attems, 1936) (Caspiopetalidae), the only ordinal representative documented from the country; a new record of Kaschmiriosoma loebli Jeekel, 2003 (Polydesmida: Paradoxosomatidae), is also provided. Localities are summarized for the 14 Pakistani, 6 Kashmirian, and 5 Bangladeshi diplopods. The last include one unidentifi able female of Zephronia Gray, 1832 (Sphaerotheriida: Zephroniidae), and two adventive species, Trachyjulus calvus (Pocock, 1893) (Spirostreptida: Cambalopsidae) and Asiomorpha coarctata (Saussure, 1860) (Polydesmida: Paradoxosomatidae); all constitute new country records. Two obscurely documented Bangladeshi diplopods are Gonoplectus cautus (Attems, 1936) (Spirostreptida: Harpagophoridae), and Trichopeltis watsoni Pocock, 1895 (Polydesmida: Cryptodesmidae). The Pakistani polydesmidan, Quasidesmus puschtun Golovatch, 1991, is transferred from Pyrgodesmidae to Cryptodesmidae.
The parajulid milliped genus Pseudojulus Bollman comprises four species: P. obtectus (Bollman), P.paynei (Hoffman), n. comb., andP. carolinensis andP. coastalis, new species; Arvechambus Causey comprises two species, A. hummi and A. weemsi, both by Causey. Georgiulus Hoffman is placed in synonymy under Fseudojulus; G. hubrichti Hoffman is placed under P. paynei; and A. australis Causey is placed under A. hummi. The genera are sympatric in north Florida and southern Georgia, but Pseudojulus extends northward to coastal South Carolina and southcentral North Carolina, and westward to Alabama west of Mobile Bay. Both genera belong to the Aniulini and possess unique features; in Pseudojulus the anterior gonopod coxae are fused into a "shelf" on the dorsal surface ofthe complex that extends ventrad along the caudal margin and possesses a pair of posterior median syncoxallobes or laminas of varying lengths and configurations. Arvechambus exhibits a suite of apomorphies and is sister to the rest of the tribe collectively: the 8th sternum possesses elevated lateral lobes that overhang the sides ofthe gonopodal aperture; the 7th pleurotergite possesses lobes that also overlie the sides of the aperture; the anterior gonopods lack lateral syncoxal processes, the coxal lobes, much larger than in other tribal genera, arise laterad and obscure part of the telopodite in anterior view, and the telopodite is elongate rather than clavate; and the 2nd pleurotergite in females possesses lobes that overhang and effectively close the cyphopodal aperture.
Previous treatments ofthe east-Nearctic spirobolid genus Narceus Rafinesque have overlooked the name, N. woodruffi Causey. The holotype is lost, but examinations of a non-typical male and two paratype and three non-typical females show it to be a valid species, perhaps endemic to north Florida, distinguished by its small size and the configurations of the gonopods and coxal lobes of legs 3-6 in males. Supplemental anatomical notes are presented on the non-typical male along with comparative drawings of the lobes and gonopods of N. woodruffi, N. american us (Beauvois), and N. annularis (Rafinesque); distributions of species of Narceus in Florida are depicted on a map. Substantial size differences between ostensibly conspecific males of N. american us in Texas and Arkansas suggest that Narceus may be more complex than the current concept
of four species.
The taxonomically neglected milliped order Glomeridesmida and family Glomeridesmidae (infraclass
Pentazonia, superorder Limacomorpha) inhabit 21, rather than seven, regions of the world, being newly recorded
from Thailand; Cambodia; the Republics of Palau, the Philippines, and Vanuatu; New Britain, Bismarck Archipelago;
the Island of New Guinea (both West Papua [formerly Irian Jaya], Indonesia, and Papua New Guinea);
and Sulawesi and Borneo, Indonesia. Occurrence in Fiji is confirmed with two additional samples, and discovery is
predicted in southern China, Myanmar, and perhaps Madagascar. Coupled with published localities, these records
suggest subcontinuous (super)ordinal and familial ranges extending some 12,480 km (7,800 mi) southeastward from
northwestern Thailand to Fiji. Though infrequently encountered, the taxa may actually be diverse and abundant
within this area, which encompasses all of the Indochina and Malay peninsulas, the Philippines, Palau, the Island
of Borneo and Indonesia, Papua New Guinea, the Solomon and Santa Cruz Islands, Vanuatu, and Fiji; it excludes
Taiwan, Australia, New Caledonia, and the Loyalty Islands. The paucity of preserved individuals probably results
from their dark pigmentations and minute sizes, adults being <6.5 mm long; Berlese extractions and sieved litter
techniques are recommended over hand collecting. Glomeridesmida are much more continuous, widespread, and
abundant in the “east” than previously believed and clearly do not comprise a minor, insignificant taxon. The first
glomeridesmidan photos are published.
Based on two “uni-ocellate” females, the world’s first introductions of the milliped order Stemmiulida are recorded from Florida, United States (US). One individual was collected in 1976 in Gainesville, Alachua County (Co.)., in northcentral peninsular Florida, and the other was taken in 1991 some 408 km (255 mi) to the south-southeast in Pompano Beach, Broward Co. The absence of further individuals and additional samples suggests that the introductions did not result in viable populations, and stemmiulidans are not presently established in the state; the Gainesville site was reinvestigated in 2012 without finding additional specimens. New records from Mexico include the first from Chiapas, Oaxaca, Tabasco, Yucatan, San Luis Potosí, and Tamaulipas states, with the northernmost ordinal locality now becoming Rancho del Cielo, northwest of Gómez Farias, in the last. A northward range expansion of about 460 km (288 mi) from the previous limit, Xalapa, Veracruz, the site lies a mere 40 km (25 mi) south of the Tropic of Cancer and only some 320 km (200 mi) south of the Rio Grande and the US border at McAllen, Hidalgo Co., Texas. Indigenous Stemmiulida are not expected in the forested Rio Grande Valley of southernmost Texas, but their occurrence in the adjoining Mexican state renders such a discovery more plausible than before.
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.
The endemic Floridian milliped genus, Floridobolus Causey, 1957, more closely related to tylobolinines in the western United States (US), Mexico, and Guatemala than syntopic spirobolines, is incorporated into Spirobolidae (Spirobolida: Spirobolidea). With taxonomic priority by one year, its monotypic family is reduced to Floridobolinae, n. stat., comprising Floridobolini and Tylobolini, n. stats., the counterpart to Spirobolinae, comprising Spirobolini and Aztecolini, n. tribe; relationships are Floridobolini + (Tylobolini + (Aztecolini + Spirobolini)). Like F. penneri Causey, 1957, 208 km (130 mi) to the south in the Lake Wales Ridge, Polk and Highlands counties (cos.), F. orini n. sp., inhabits “Big Scrub” environments in the Ocala National Forest, Marion Co. Biogeographic reconstructions, compatible with broader hypotheses on the class’ evolutionary history, indicate that, from a presumptive source area in northern Mexico where the subfamilies overlap, spirobolid stock penetrated the “proto-US” four times, once per tribe, before the Western Interior Seaway developed in the Cretaceous Period, Mesozoic Era. Three expansions headed northeastward into future “Appalachia,” from which taxa spread southward as the Seaway receded. Floridobolini, the fi rst invader, had to be in “proto-Georgia” and positioned to penetrate Florida when the sand dunes that comprise the “Central Highlands” emerged from the sea in the Oligocene (Cenozoic), ~25 mya. As sea levels rose and fell, the dunes fragmented into islands and the subcontinuous Floridobolus population was partitioned. The southernmost became F. penneri; F. orini inhabited a northern island; and a graduate student is investigating other insular remnants for additional species. Shortly after Floridobolini began spreading, Hiltonius/ Tylobolini arose and expanded both southward to Guatemala and northwestward to California; Tylobolus Cook, 1904, diverged in the latter area and dispersed northward to Washington and eastward to Utah/Arizona. The third invader, and the second to disperse northeastward, was Aztecolini, which probably eradicated Floridobolini from some of its established range and was partitioned into Mexican (Aztecolus Chamberlin, 1943) and US (Chicobolus Chamberlin, 1947) taxa by the Seaway. The fi nal invader, Spirobolini, dispersed northwestward and northeastward to both the Pacifi c and Atlantic coasts; instead of Trans-Beringia, we prefer penetration of the Asian part of “Asiamerica,” when it temporarily formed during the Cretaceous, to explain the Mongolian fossil genus, Gobiulus Dzik, 1975, herein assigned to Tylobolini, and the occurrence of Spirobolus Brandt, 1833, in China and Taiwan today. In the east, Narceus Rafi nesque, 1820, spread across Appalachia, eradicated most remaining populations of Floridobolus and Chicobolus, and expanded to Maine and Québec after retreat of the Wisconsin glaciation. Chicobolus and Narceus also penetrated earliest Florida; the former established itself in the Central Highlands, spread through the widening peninsula as sea levels fell, and remained on insular refugia when waters rose. Apparently fueled by the different Floridian environments, Narceus underwent time-consuming speciation; consequently, Floridobolus and Chicobolus still survive on the peninsula, and an allopatric population of the latter inhabits coastal South Carolina. However, N. gordanus (Chamberlin, 1943) occurs syntopically with both in peninsular Florida and may be actively eradicating them from their last stronghold. Trigoniulus niger, takahasii, and segmentatus, all by Takakuwa, 1940, are removed from Spirobolidae and returned toTrigoniulidae (Trigoniulidea). New records in the Appendix include the fi rst of Aztecolus from Durango and Jalisco, Mexico.