Insecta Mundi
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0469
0468
Pyroghatsiana, a new genus of pyrochroine Pyrochroidae is described from the Southern Ghats of the Indian continental southern tip. The only known specimen is a female, Pyroghatsiana madurensis (Pic), new combination, originally placed in Dendroides Latreille, and subsequently transferred to Pseudodendroides Blair. Several striking differences including the dorsal interocular width between the compound eyes, shape and length of the third antennal segment, and shape of the pronotum preclude placement of Pyroghatsiana in either Dendroides, Pseudodendroides, or any other existing pyrochroine genus.
0467
We provide the current holdings of Meropeidae in the Florida State Collection of Arthropods (FSCA). To date, FSCA holds a well-curated collection of extant meropeids representing 17 U.S. states and Western Australia (n = 316 Merope tuber Newman, fi ve Austromerope poultoni Killington). Merope tuber records from Vermont, Texas, and South Carolina are published here for the fi rst time. A total of 298 pinned M. tuber and four pinned
A. poultoni; six M. tuber specimens preserved in 95% ethanol; and 12 M. tuber and one A. poultoni sputter-coated with gold-palladium for SEM are available for researchers interested in studying this unique family of insects.
0466
Carulaspis juniperi (Bouché) is newly documented as occurring in the Korean fauna of armored scales (Hemiptera: Diaspididae). The characters of this genus and species are redescribed based on specimens collected in Korea. In addition, four species of aphelinids (Hymenoptera: Aphelinidae) associated with C. juniperi were collected in Korea during the survey. Of these, Aphytis japonicus DeBach and Azim and Encarsia explorata (Silvestri) are recorded for the fi rst time from C. juniperi.
0465
Scale insects (Hemiptera: Coccoidea) of avocado, Persea americana Mill. (Lauraceae) were collected in the State of Valle del Cauca, Colombia. The study was conducted for one year, during October 2008–October 2009.
As a result of this study, 34 scale insect species in seven families (Coccidae, Diaspididae, Kerriidae, Margarodidae,
Monophlebidae, Pseudococcidae and Putoidae) were collected. Together with previous records, the number of scale insects collected on avocado in Colombia increased to 44 species and to 137 species worldwide. Species commonly collected on avocado in Colombia include Hemiberlesia cyanophylli (Signoret), Pseudoparlatoria parlatorioides (Comstock) (Diaspididae), Ceroplastes rubens Maskell, Coccus hesperidum L., Protopulvinaria pyriformis (Cockerell), Pulvinaria psidii Maskell, Saissetia neglecta De Lotto (Coccidae) and Ferrisia williamsi Kaydan and Gullan (Pseudococcidae). Twenty-two scale insect species are new records on avocado for Colombia of which nine species are new records worldwide, namely, Lindingaspis rossi (Maskell), Pseudischnaspis bowreyi (Cockerell) (Diaspididae), Pulvinaria psidii Maskell, Saissetia neglecta De Lotto (Coccidae), Ferrisia kondoi Kaydan and Gullan, Pseudococcus jackbeardsleyi Gimpel and Miller, Ps. landoi (Balachowsky) (Pseudococcidae), Eurhizococcus colombianus Jakubski (Margarodidae) and Austrotachardiella colombiana Kondo and Gullan (Kerriidae).
0464
0463
The name Melolontha hypocrita Mannerheim, 1829 has been long unused, even though it is the type species of Hyporhiza Dejean, 1833. I examined the only known specimen from the type series and here designate it as the lectotype. Examination of this lectotype reveals that this species is best placed in the genus Rhinaspis Perty, 1830. Consequently, the genus Hyporhiza Dejean, 1833 is confi rmed as a junior synonym of Rhinaspis. Further, the replacement name Rhinaspis fuhrmanni is proposed for Rhinaspis hypocrita (Blanchard, 1850), a new secondary homonym of Rhinaspis hypocrita (Mannerheim, 1829). A homonymy problem was also discovered and corrected for the genus Plectris LePeletier and Serville, 1828. The replacement name Plectris schoolmeestersi is proposed for Plectris paraguayensis Moser, 1924, which is a secondary junior homonym of Plectris paraguayensis (Moser, 1921).
0462
0461
Epimelitta postimelina Giesbert, 1996 and Odontocera apicula Bates, 1885 are transferred to the new genus Odontomelitta. Epimelitta postimelina, with closed procoxal cavities, cannot remain in Epimelittta Bates, 1870, a genus characterized by open procoxal cavities. The short elytra and tegmen (with caliper-shaped lateral lobes) of the aedeagus of both species excludes them from the genus Odontocera Audinet-Serville, 1833, with long elytra and tegmen (with strap-shaped lateral lobes). Both species are illustrated, and host plant and host flower records provided for O. apicula.
0460
The island arc of the Lesser Antilles lies at the eastern margin of the Caribbean Sea in the Western Hemisphere, and stretches from the eastern end of the islands of the Greater Antilles (at the Virgin Islands), south to a position near the continental islands of Trinidad and Tobago at the north eastern corner of South America. The islands are a part of the West Indian Islands biodiversity “hotspot” and have been available for terrestrial colonization for about the past 15 million years. This is a status report on present knowledge of the beetle faunas of these islands, which is composed of 90 families, 1210 genera, and 2612 recognized species. Many additional species are not yet identified, or are unnamed, or remain to be discovered. Reported for the first time from the Lesser Antilles are four families, 49 genera, 105 species, and 1253 new island records. The largest families are Curculionidae (588 species), Staphylinidae (389 species), Chrysomelidae (181 species), Tenebrionidae (142 species), Cerambycidae (138 species), Scarabaeidae (127 species), and Carabidae (126 species). There are differing patterns of species distributions: 154 species are probably introduced by human activities; 985 are endemic species (limited to a single island); 465 are species endemic to more than one island of the Lesser Antilles; 212 are species limited to just islands of the West Indies; and 800 are native (naturally occurring) species which also have part of their distributional range in North, Central, or South America. Most of the widely distributed beetle fauna has probably come from South America by over-water dispersal. There is no compelling evidence for a vicariance origin of any part of the beetle fauna. Earlier colonists have had more time to form endemic genera (18) and endemic species. The more widely distributed species probably represent distributions achieved in and since the Pleistocene.