Insecta Mundi
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870
The soybean aphid, Aphis glycines Matsumura (Hemiptera: Aphididae), is a major pest of soybean, Glycine max (L.) Merr., both in Asia where it is native, and in the USA where it is adventive. The rapid spread and establishment of the soybean aphid in the USA since its discovery in 2000 was successful because of extensive soybean production in the Midwest and the wide distribution of common buckthorn, Rhamnus cathartica (L.), its preferred primary winter host. The survivorship of four soybean aphid biotypes on common and glossy buckthorn, Frangula alnus Mill., were compared. Our study showed that nymph oviparae of soybean aphid biotypes 1, 2, 3 and 4 reached adulthood and produced eggs on glossy buckthorn. When comparing morphs between the hosts, greater numbers were recorded on common than glossy buckthorn, with one exception where the number of eggs per bud for soybean aphid biotype 2 was not different between the hosts. We found for the first-time soybean aphid biotypes 2 and 3 apterous males produced on common and glossy buckthorn. Morphological descriptions of live and mounted alate and apterous males are presented.
869
New adult host records of Agrilus langei Obenberger, A. pilosicollis Fisher, and Dicerca mutica LeConte (Coleoptera: Buprestidae) are reported. The known geographic range of A. pilosicollis is expanded from the type location in Kansas south to Texas and east to North Carolina. Images with key characters of each of the three species are included.
868
We recognize and review 40 species of Chlamydastis Meyrick, 1916 (Lepidoptera: Depressariidae) from Costa Rica, including four previously described (i.e., C. vividella (Busck, 1914), revived status; C. phytoptera (Busck, 1914); C. orion Busck, 1920; and C. ungulifera (Meyrick, 1929)) and 36 new species: C. abelulatei Phillips and Brown, new species; C. carolinagodoyae Phillips and Brown, new species; C. angelsolisi Phillips and Brown, new species; C. lindapitkinae Phillips and Brown, new species; C. iangauldi Phillips and Brown, new species; C. anniapicadoae Phillips and Brown, new species; C. antonioazofeifai Phillips and Brown, new species; C. mignondavisae Phillips and Brown, new species; C. marianofigueresi Phillips and Brown, new species; C. colleenhitchcockae Phillips and Brown, new species; C. bernardoespinozai Phillips and Brown, new species; C. bobandersoni Phillips and Brown, new species; C. carlosviquezi Phillips and Brown, new species; C. christerhanssoni Phillips and Brown, new species; C. christhompsoni Phillips and Brown, new species; C. paulhansoni Phillips and Brown, new species; C. elenaulateae Phillips and Brown, new species; C. gladysrojasae Phillips and Brown, new species; C. powelli Phillips and Brown, new species; C. gracewoodae Phillips and Brown, new species; C. juanmatai Phillips and Brown, new species; C. isidrochaconi Phillips and Brown, new species; C. jimlewisi Phillips and Brown, new species; C. jimmilleri Phillips and Brown, new species; C. montywoodi Phillips and Brown, new species; C. johnnoyesi Phillips and Brown, new species; C. luisdiegogomezi Phillips and Brown, new species; C. paulthiaucourti Phillips and Brown, new species; C. dondavisi Phillips and Brown, new species; C. irenecanasae Phillips and Brown, new species; C. manuelzumbadoi Phillips and Brown, new species; C. noramartinae Phillips and Brown, new species; C. vitorbeckeri Phillips and Brown, new species; C. ronaldzunigai Phillips and Brown, new species; C. munifigueresae Phillips and Brown, new species; and C. willsflowersi Phillips and Brown, new species.COI nucleotide sequences (“DNA barcodes”) were obtained for 33 of the species, which helped associate males with females for sexually dimorphic species and revealed a few cryptic, presumably evolutionary siblings. We illustrate adults of all species, along with their male and female genitalia, where available.Nineteen species were reared from caterpillars, and their foodplants are listed. In Costa Rica, 15 species of Chlamydastis are recorded exclusively from Sapotaceae; one species each exclusively from Clethraceae, Vochysiaceae, Combretaceae, and Melastomataceae. Larvae are illustrated for 10 of the 36 new species, and superficial larval descriptions are provided based on photographs and notes. Of the 40 species of Chlamydastis reported from Costa Rica, 32 have been light-collected or reared from Área de Conservación Guanacaste.
867
The relationship between the beetle family Eucnemidae and the parasitic proctotrupoid family Vanhorniidae is discussed. The only proven host for Vanhornia eucnemidarum Crawford in North America is an undetermined species of the genus Isorhipis Boisduval and Lacordaire. In Europe, the only known host for Vanhornia leileri Hedqvist is Hylis cariniceps (Reitter). The biologies of the hosts differ radically and it appears unlikely that they could be parasitized in a typical proctotrupoid fashion in which eggs are placed in or on the host larva. This supports the hypothesis that small Vanhorniidae larvae attach themselves to the newly hatched beetle larvae, before they enter the wood on which they feed. The taxonomy of the genus Vanhornia Crawford is briefly discussed.
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865
A new genus, Cicatrisphaerion Lingafelter, Morris, Skillman, and Santos-Silva (Coleoptera: Cerambycidae), and three new species of the same authorship, C. wappesi from Quintana Roo, Mexico, C. rileyi from Chiapas, Mexico, and Eupogonius wappesi from Quintana Roo, Mexico, are described. New records and clarification on the distribution of Psyrassaforma janzeni Chemsak, 1991 and P. nitida Chemsak, 1991 are provided. Ameriphoderes amoena (Chemsak and Linsley, 1979) is redescribed based on four male specimens and a new country record from Guatemala is documented. New distributional records are provided for Estola flavobasalis Breuning, 1940 (including a new country record for Bolivia) and Estola vittulata Bates, 1874. A redescription and new distributional record are provided for Eupogonius flavovittatus Breuning, 1940 based on a female specimen.
864
The tribe Platynini (Coleoptera: Carabidae: Harpalinae) is revised for New Zealand. Eight genera and forty-three species are recognized. Four genera and sixteen species are described as new: Ctenognathus davidsoni Larochelle and Larivière new species, Ctenognathus earlyi Larochelle and Larivière new species, Ctenognathus garnerae Larochelle and Larivière new species, Ctenognathus hoarei Larochelle and Larivière new species, Ctenognathus kaikoura Larochelle and Larivière new species, Ctenognathus marieclaudiae Larochelle new species, Ctenognathus perumalae Larochelle and Larivière new species, Ctenognathus takahe Larochelle and Larivière new species, Ctenognathus tawanui Larochelle and Larivière new species, Ctenognathus tepaki Larochelle and Larivière new species, Ctenognathus urewera Larochelle and Larivière new species, Kiwiplatynus Larochelle and Larivière new genus, Kiwiplatynus taranaki Larochelle and Larivière new species, Kupeplatynus Larochelle and Larivière new genus, Maoriplatynus Larochelle and Larivière new genus, Maoriplatynus marrisi Larochelle and Larivière new species, Prosphodrus mangamuka Larochelle and Larivière new species, Prosphodrus sirvidi Larochelle and Larivière new species, Prosphodrus waimana Larochelle and Larivière new species, Tuiplatynus Larochelle and Larivière new genus. Lectotypes are designated for twelve taxa: Anchomenus adamsi Broun, 1886, Anchomenus colensonis White, 1846, Anchomenus feredayi Bates, 1874, Anchomenus helmsi Sharp, 1881, Anchomenus intermedius Broun, 1908, Anchomenus macrocoelis Broun, 1908, Anchomenus munroi Broun, 1893, Anchomenus sophronitis Broun, 1908, Colpodes crenatus Chaudoir, 1878, Colpodes neozelandicus Chaudoir, 1878, Ctenognathus littorellus Broun, 1908, and Ctenognathus pictonensis Sharp, 1886.Six new combinations are established: Ctenognathus bidens (Chaudoir, 1878) = Kiwiplatynus bidens (Chaudoir, 1878); Ctenognathus crenatus (Chaudoir, 1878) = Kupeplatynus crenatus (Chaudoir, 1878); Ctenognathus lucifugus (Broun, 1886) = Kupeplatynus lucifugus (Broun, 1886); Ctenognathus sulcitarsis (Broun, 1880) = Kupeplatynus sulcitarsis (Broun, 1880); Ctenognathus libitus (Broun, 1914) = Tuiplatynus libitus (Broun, 1914); Ctenognathus sophronitis (Broun, 1908) = Tuiplatynus sophronitis (Broun, 1908).Fifteen new synonymies are established: Ctenognathus littorellus Broun, 1908 = Ctenognathus adamsi(Broun, 1886); Anchomenus parabilis Broun, 1880 = Ctenognathus cardiophorus (Chaudoir, 1878); Anchomenus integratus Broun, 1908 = Ctenognathus colensonis (White, 1846); Anchomenus macrocoelis Broun, 1908 = Ctenognathus edwardsii (Bates, 1874); Ctenognathus actochares Broun, 1894 = Ctenognathus elevatus(White, 1846); Anchomenus punctulatus Broun, 1877, Anchomenus montivagus Broun, 1880, Anchomenus perrugithorax Broun, 1880, Anchomenus politulus Broun, 1880, Anchomenus suborbithorax Broun, 1880, and Colpodes neozelandicus Chaudoir, 1878 = Ctenognathus novaezelandiae (Fairmaire, 1843); Ctenognathus simmondsi Broun, 1912 = Ctenognathus pictonensis Sharp, 1886; Anchomenus (Platynus) cheesemani Broun, 1880 and Calathus deformipes Broun, 1880 = Kupeplatynus crenatus (Chaudoir, 1878); Anchomenus munroi Broun, 1893 = Kupeplatynus lucifugus (Broun, 1886). Ctenognathus elevatus (White, 1846), previously synonymized with Ctenognathus novaezelandiae (Fairmaire, 1843), is reinstated as full species. A revision of all taxa is provided. Descriptions, identification keys, illustrations of male genitalia, habitus photos, distributional data and maps are given. Extensive information on ecology, biology, dispersal power, and collecting techniques is included for each species.
863
862
861
Peru’s Cosñipata Region in Cuzco and Madre de Dios Departments is a valley between Manu National Park and the Amarakaeri Communal Reserve that ranges from 400 to 4,000 m elevation. A team of experienced lepidopterists sampled the butterfly fauna of this valley for more than a decade (7,440 field person-hours). We analyze the data for Lycaenidae (Lepidoptera: Papilionoidea), a family for which we have taxonomic expertise. After adding data on the fauna from museums and the literature, we present an annotated checklist of the 340 Lycaenidae species recorded from the Cosñipata Region with notes for each species on the elevations and seasons at which it occurs, adult behavior, and sampled relative abundance. Species richness is twice that recorded for Trinidad or Brazil’s Parque Nacional do Itatiaia, each of which also has a mix of low, mid, and high elevation habitats. There was an average of 8.3 adult specimens per species in the fieldwork sample. For those species with more than 8 specimens, the median elevational range was 1,100 m. Species richness in low elevation habitats was greater than that at mid or high elevations, which is contrary to findings for some other Neotropical insects. We present evidence why further sampling is likely to increase this difference. Maximal adult species richness occurs during the transition from dry to wet seasons (September to November) at all elevations, but there is little evidence that adults of species occur only during this season. Sampled relative abundances were skewed so that 70% of the species were encountered less frequently than average (1/340). These results are consistent with the observation that most species are rarely encountered using standard sampling methods.