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The taxonomic position of Onthophagus (Palaeonthophagus) lemuroides d’Orbigny, 1898 and Onthophagus
(Palaeonthophagus) fortigibber Reitter, 1909 is discussed (Coleoptera: Scarabaeidae: Scarabaeinae: Onthophagini).
A key to the species is given. Photos of type specimens of the two taxa and significant chromatic varieties, and
drawings of aedeagi are presented.
Evidence is presented that the subspecies Chrysobothris thoracica guadeloupensis Descarpentries, 1981
(Coleoptera: Buprestidae) should be recognized at the species level. Character evidence is provided to separate C.
guadeloupensis, new status, from C. thoracica Fabricius, 1798. Both species are illustrated with habitus photographs
and images of the male genitalia.
Acoma howdenorum, Acoma westcotti, Acoma quadrilaminata, and Acoma cimarron (Coleoptera: Scarabaeidae: Melolonthinae), all new species, are described from Yuma County, Arizona, USA, and Baja California Sur, Baja California (Norte), and Sonora, Mexico, respectively. Habitus of the four new species is illustrated, and an updated key to the described species in the genus is provided. Distribution and variation of Acoma glabrata Cazier are also discussed.
The Orizabus Fairmaire (Coleoptera: Scarabaeidae: Dynastinae: Pentodini) of the USA are reviewed. Orizabus pinalicus new species and O. mcclevei new species are described. Lectotypes are here designated for eight species names: Bothynus pyriformis LeConte, Pseudaphonus lucidus Casey, Orizabus snowii Horn, Orizabus cultripes Fairmaire, Orizabus isodonoides Fairmaire, Orizabus sallei Fairmaire, Orizabus fontinalis Casey, and Orizabus ponderosus Casey. Illustrations of diagnostic characters and a key to the five included species are presented. The Mexican species O. isodonoides and O. rubricollis Prell are also illustrated for comparison to the new species.
The female of Nothopleurus subsulcatus (Dalman, 1823) (Coleoptera: Cerambycidae: Prioninae: Macrotomini) is described for the first time, and the female of Strongylaspis bullata Bates, 1872 is redescribed. Color photographs of the habitus of both, and key characters for the former are included. New distributional records within Mexico for N. subsulcatus and Strongylaspis championi Bates, 1884 are given.
An additional 137 species and two tribes are added to the cerambycid fauna of Bolivia while 12 species are deleted. This brings the total number of species known from Bolivia to 1,561. Comments and statistics regarding the growth of knowledge on the Bolivian Cerambycid fauna and species endemicity are included.
I add new collection and phenological data on the North American earwigfly, Merope tuber Newman, and new county records for the red scorpionfly, Panorpa rufa Gray, and veined scorpionfly, Panorpa venosa Westwood, in Florida. Additionally, I report on a new Georgia county record for the extralimital species, Panorpa ferruginea Byers, the ferruginous scorpionfly, and speculate on its potential occurrence in Florida.
Five new species of anilline ground beetles (Carabidae: Trechinae: Bembidiini) are described from the Appalachian Mountains and Piedmont Plateau of eastern United States. Two species, Anillinus unicoi n. sp. (from the Unicoi Mountains, North Carolina) and A. carltoni n. sp. (from the Great Smoky Mountains, North Carolina/Tennessee), inhabit the crests of adjacent mountain ranges, and share similarities with A. moseleyae Sokolov and Carlton. These three comprise a high-altitude group of species in the region. The third species A. chilhowee n. sp. is one of the smallest representatives of the loweae-group of species. It differs from its relatives in characters of male genitalia and inhabits the isolated Chilhowee Mountain ridge between Ocoee and Hiwassee Rivers (Polk County, Tennessee). The fourth and fifth species possess complex arrays of spines on the internal sac of the aedeagus, similar to A. valentinei (Jeannel) from caves of Alabama. In the case of A. smokiensis n. sp. (Gregory Cave, Great Smoky Mountains National Park, Tennessee), the aedeagal similarity suggests a close relationship with A. valentinei. Anillinus chandleri n. sp. from the Piedmont Plateau (Sumter National Forest, South Carolina) is similar to A. cornelli Sokolov and Carlton, also described from the Carolina Piedmont region. Keys are provided for the new species, where possible.
Saba Island (Caribbean Netherlands) is one of the northernmost islands of the Lesser Antilles. It is only 13 square kilometers but contains a wide variety of potential spider habitats including dry, moist, and elfin forests. As part of a collaborative effort between Conservation International and Saba Conservation Foundation, during a several week period in March and May 2008 we briefly surveyed the island for spiders and other arthropods. This survey, the first for spiders of Saba, resulted in the identification of 18 families and 76 spider species, including six new species that will be described elsewhere and may be endemic to Saba. The species richness of Saba’s spider fauna is considerably higher than that reported from other small Caribbean islands. We conclude this is probably a combined result of undersampling and lower habitat diversity on these other islands.
The diplopod orders Callipodida and Polydesmida, and their respective families Abacionidae and
Xystodesmidae, are initially recorded from South Dakota as is Polydesmidae from North Dakota. Other new records of
indigenous taxa include Abacion Rafinesque, 1820/A. texense (Loomis, 1937) and Pleuroloma/P. flavipes, both by
Rafinesque, 1820, from South Dakota, and Pseudopolydesmus Attems, 1898/P. serratus (Say, 1821) from Alabama,
Connecticut, Delaware, New Hampshire, North Dakota, South Carolina, and the District of Columbia. New records of
Aniulus garius Chamberlin, 1912, A. (Hakiulus) d. diversifrons (Wood, 1867), and Oriulus venustus (Wood, 1864)
(Julida: Parajulidae) are provided for western Minnesota and/or eastern North Dakota. Published records from these
states are summarized, and the introduced taxa, Julidae/Cylindroiulus Verhoeff, 1894/C. caeruleocinctus (Wood, 1864)
and Paradoxosomatidae/Oxidus Cook, 1911/O. gracilis (C. L. Koch, 1847), are newly recorded from the Dakotas. The
distribution of P. serratus, which extends from Maine to South Carolina and the Florida panhandle, west to Texas, and
north to Fargo, North Dakota is described and discussed. This distribution exhibits a prominent southeastern lacuna
which we hypothesize suggests replacement by younger, more successful species, as postulated for a similar distributional
gap in Scytonotus granulatus (Say, 1821).
The milliped genus Euryurus Koch, 1847, and the species, E. leachii (Gray, 1832) (Polydesmida: Euryuridae), are recorded from three sites on the northern part of Crowley’s Ridge (Cross, Lee, and Poinsett counties), Arkansas, where the only prior familial records are of Auturus evides (Bollman, 1887). Coupled with the published locality of E. leachii in Phillips Co., at the southern extremity of the Ridge, the only known occurrences of both the genus and species in Arkansas and west of the Mississippi River are in this physiographic feature. The Arkansas population is geographically peripheral but anatomically intermediate between the two recognized subspecies, E. l. leachii and E. l. fraternus Hoffman, 1978, and we do not assign it to a race. Molecular investigations seem necessary to resolve relationships in the “E. leachii complex.”
The biogeographic significance of Diplopoda is substantiated by 50 maps documenting indigenous occurrences of the 16 orders, the three Spirostreptida s. l. suborders – Cambalidea, Epinannolenidea, Spirostreptidea – and all higher taxa including Diplopoda itself. The class is indigenous to all continents except Antarctica and islands/archipelagos in all temperate and tropical seas and oceans except the Arctic; it ranges from Kodiak Island and the northern Alaskan Panhandle, United States (USA), southern Hudson Bay, Canada, and near or north of the Arctic Circle in Iceland, continental Scandinavia, and Siberia to southern “mainland” Argentina, the southern tips of Africa and Tasmania, and Campbell Island, subantarctic New Zealand. The vast, global distribution is interrupted by sizeable, poorly- or unsampled areas including the Great Basin, USA; the Atacama Desert region of Chile and neighboring countries; southern South American islands; the central Kalahari and Sahara deserts; the Gobi Desert, Mongolia, and all of north-central and western China; from north of the Caspian Sea, Russia, to central Kazakhstan; and the “Outback” of central Australia. Five Arabian countries lack both samples and published records of indigenous diplopods – Bahrain, Kuwait, Oman, Qatar, and United Arab Emirates – as do Turks and Caicos, in the New World, and Mauritania and possibly Egypt, Africa. New records, including the first for Chilognatha from Botswana and the first specific localities from Northern Territory, Australia, are cited in the Appendix. Increased emphasis on mappings in taxonomic research is warranted along with investigations of insular “species swarms” that constitute a microcosm of the early evolution of the class. The largest “species swarm” in the Diplopoda is Diplopoda itself!
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.