Insecta Mundi
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0378
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.
0423
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.
0418
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.
571
A trimaculate male of the diplopod genus Apheloria Chamberlin (Polydesmida: Xystodesmidae/-inae: Apheloriini) from 1.3 km (0.8 mi) west of McKenney, Dinwiddie County (Co.), Virginia, is designated the Neotype of Julus virginiensis Drury 1770, thereby stabilizing the earliest name for a North American milliped and authenticating its prior assignment to this taxon. The existing concept of Apheloria is accepted in the absence of a revisionary treatment, and a modern description of A. v. virginiensis with gonopod drawings and color photos is provided. Drury’s original account and his letter to the Virginian who sent him the original specimens are quoted verbatim to eliminate future library searches. The specific name has been associated with at least three genera, and its confusing history is clarified by summarizing works in each. Authentic localities, mapped to the extent now possible, reveal a distribution south of the James River in piedmont and coastal Virginia that extends southwestward to the Blue Ridge foothills and at least as far south in North Carolina (NC) as Greensboro, the “Triangle” (Raleigh/Durham/Chapel Hill region), and Albemarle Sound in the east. Based on the holotypes, A. aspila and A. tigana, both by Chamberlin, are placed in synonymy under A. v. virginiensis (syns. nov.), and although its status is still under review, A. waccamana Chamberlin, whose type locality is Lake Waccamaw, Columbus Co., in southeastern NC, may be the correct name for today’s A. tigana. All samples so labeled must be reexamined for misidentifications of A. v. virginiensis.
743
The following five species of Dermestidae (Coleoptera) are recorded for the first time from Guatemala: Attagenus fasciatus (Thunberg), Dermestes (Dermestinus) caninus caninus Germar, Orphinus fulvipes (Guérin-Méneville), Trogoderma simplex Jayne and Thorictodes heydeni Reitter. The species are recorded from the Guatemalan departments of Petén, Izabal and Zacapa.
0161
573
With an incident in Palo Duro Canyon, Texas, USA, Scolopendra heros Girard (Chilopoda: Scolopendromorpha: Scolopendridae) becomes the third centipede species known to prey on bats; S. gigantea Linnaeus and S. viridicornis Newport have been so documented in Venezuela and Brazil, respectively. The Texas predation was interrupted by the predator/prey pair’s falling around 15–20 m from the canyon wall and, perhaps also, by human presence where they landed. The centipede uncoiled and retreated to shelter under a nearby rock and, after initial immobilization, so did the bat.
0023
A generic-level phylogenetic review of the Macrodactylini (Coleoptera: Scarabaeidae: Melolonthinae)
(2007)
A revision of the generic classification of the tribe Macrodactylini is provided using morphological characters of adults. The revision is based on a taxonomic analysis of 80 genera historically placed in the tribe and a cladistic analysis of 32 genera conforming to the new tribal definition. Synapomorphies for the newly defined Macrodactylini include: the length of the fifth ventrite longer than the fourth ventrite when viewed ventrally, fifth ventrite lacking a complete suture between the tergite and sternite, and the metathoracic tibial spurs (if present) offset, allowing the metatarsus to move past them. Thirty-two genera constitute the newly defined Macrodactylini: Agaocnemis Moser, Alvarinus Blanchard, Ancistrosoma Curtis, Anomonyx Saylor, Anoplosiagum Blanchard, Astaenosiagum Martínez, Barybas Blanchard, Calodactylus Blanchard, Ceraspis Le Peletier and Serville, Ceratolontha Arrow, Chariodactylus Moser, Chariodema Blanchard, Chremastodus Solier, Clavipalpus Laporte, Ctenotis Burmeister, Dasyus Le Peletier and Serville, Dicrania Le Peletier and Serville, Gama Blanchard, Gastrohoplus Moser, Hercitis Burmeister, Hieritis Burmeister, Isonychus Mannerheim, Issacaris Fairmaire, Macrodactylus Dejean, Manodactylus Moser, Manopus Laporte, Oedichira Burmeister, Pectinosoma Arrow, Plectris Le Peletier and Serville, Pristerophora Harold, Rhinaspis Perty, and Schizochelus Blanchard. Sixteen genera are removed or their removal is confirmed from the historical Macrodactylini: Coenonycha Horn, Dichelonyx Harris, and Gymnopyge Linell (to Dichelonychini), Homalochilus Blanchard, Homoliogenys Gutiérrez, Liogenys Guérin-Méneville, and Pacuvia Curtis (to Diplotaxini), Diphycerus Deyrolle and Fairmaire (to Diphycerini), Hyperius Deyrolle and Fairmaire (to Melolonthini), Apterodemidea Gutiérrez (to Sericoidini), Blepharotoma Blanchard (to Liparetrini ), Diaphylla Erichson (removed from Macrodactylini, and currently unplaced into existing melolonthine tribes), Hilarianus Blanchard, Manonychus Moser, Pseudoisonychus Frey (removed from Macrodactylini, and currently unplaced into existing melolonthine tribes) and Zabacana Saylor (to Epectinaspis (Rutelinae)). Nine new generic synonyms are proposed: Corminus Burmeister, junior synonym of Alvarinus Blanchard; Ctilocephala Burmeister, Eubarybas Gutiérrez, and Pseudohercitis Moser, each a junior synonym of Barybas Blanchard; Byrasba Harold, Rhinaspoides Moser, and Ulomenes Blanchard, each a junior synonym of Rhinaspis Perty; Demodema Blanchard, a junior synonym of Plectris Le Peletier and Serville; and Pachylotoma Blanchard, junior synonym of Gama Blanchard.
0004
Published claims in 1887-1903 that the mole cricket Neocurtilla hexadactyla (Perty) occurs in Puerto Rico all seem to be derived from a misidentification made by Agustín Stahl, a medical practitioner and collector of natural history objects, published in 1882. That species does not seem now to occur in Puerto Rico and almost certainly never did. However, the opportunity still exists for it to colonize by wind-assisted flight from islands to the southeast just as we believe did the mole cricket Scapteriscus didactylus (Latreille) as an immigrant. Stahl evidently mistook the latter for the former. According to some subsequent authors, he also stated that it (the mole cricket now believed to be S. didactylus) arrived in the port of Mayagüez in a cargo of guano about 1850 from Peru and thus colonized Puerto Rico. We found no verification for that story, and we doubt it. The first detection of the presence of S. didactylus in Puerto Rico may have been by a French expedition in 1797, but this species may have been present much earlier. Two other species of Scapteriscus were later detected in Puerto Rico. One, S. abbreviatus Scudder, was detected in 1917 and likely arrived as a contaminant of ship ballast some time earlier, perhaps at the port of Mayagüez. The other, S. imitatus Nickle and Castner, was detected about 1940 and seems to have been introduced inadvertently, as a result of mistaken identity. In broad terms, S. didactylus, S. abbreviatus, and S. imitatus are adventive species (meaning they arrived from somewhere else and are not native) in Puerto Rico. The vernacular name changa in Puerto Rico is owned by S. didactylus, which is called West Indian mole cricket in the English-speaking Caribbean. Historical accounts suggest that populations of S. didactylus and of two pest Phyllophaga spp. (Coleoptera: Scarabaeidae) surged after 1876/1877 and declined after 1920. This coincidence suggests that the cause may have been the same. The cause of the rise might conceivably have been introduction of the mongoose Herpestes javanicus (E. Geoffroy St. Hilaire) in 1877 (because it may have destroyed vertebrate predators) and the cause of the decline might conceivably have been introduction of the toad Bufo marinus L. in 1920, because it is a predator of Phyllophaga and Scapteriscus.
0367
A gomphid male from west-central Wisconsin (Eau Claire County, North Fork Eau Claire River, 11 June 1994, K. J. Tennessen leg) with characters that are intermediate between Ophiogomphus carolus Needham, 1897 and Ophiogomphus rupinsulensis (Walsh), 1862 is described and illustrated. The specimen appears to be a hybrid based on intermediate character states of 1) color pattern (slightly closer to O. carolus), 2) hamule morphology (shaped slightly more like those of O. carolus), and 3) anal appendage morphology (slightly more like those of O. rupinsulensis).