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Three new species of the albomarginatus species group of the genus Trachysphyrus (T. fidalgoi, T. riojanus, and T. tmetus) are described from the Subandean Desert (Monte) of Northwest Argentina. A key is given to these and to the five described species also known from Neotropic Argentina in the semiarid Prepuna, Subandino, and Chaco Serrano as well as in such wetter habitats as the Chaco Húmedo and Selva Tucumano-Boliviana (Yungas). Four additional species occur in Neantarctic Chile from Santiago south to Magallanes with overlap into the Nothofagus forests of southwest Argentina (Neuquén, Río Negro). Several species have been reared from cocoons of Lepidoptera (Megalopygidae, Psychidae) and others from mud nests of eumenid wasps (Hypodynerus Saussure, Pachymenes Saussure).
The origins of the Cuban bee fauna are reviewed. This fauna began to form 40 million years ago during the Proto Antilles period, through ancestors that arrived in successive invasions from adjacent continental areas. The composition of the Antillean fauna has evolved continuously over millions of years until the present time. The native bee fauna of Cuba is represented by 89 species, contained in 29 genera and 4 families. The number of genera represented per family is as follows: Colletidae (3), Halictidae (8), Megachilidae (4), and Apidae (14). The Cuban apifauna contains four principal groups with distinct biogeographic histories: endemic species of Cuba (43.8%); endemic species of the Antilles shared among multiple islands (33.1%); continental species whose distribution includes the Antilles (16.8%); and species introduced through human activity (6.3%). An analysis of the distributions of Cuban bee species reveals that areas of highest species endemism coincide with the main mountainous nuclei of the East, Center and West. These were: the Sierra Maestra mountain range (with 25 species), Nipe-Sagua-Baracoa (15), the Mountain range of Guaniguanico (14) and the Massif of Guamuaya (14). The distribution of the bees in the Cuban Archipelago was not uniform, possibly due to the ecological conditions of the respective habitats, the diversity and presence of specific food plants, and interspecific competition. The endemism of bees in Greater Antilles is considered high keeping in mind the mobility of the group, as observed not only in Cuba (43.8%) but also Jamaica (50%), Hispaniola (45.6%), and in Puerto Rico and adjacent islands (26.5 %).
In the eastern United States, the genus Cotinis Burmeister previously contained only C. nitida (L.), the common economic pest known as the "Green June Beetle". A new species from the Florida Keys, Cotinis aliena, is here described and illustrated. A checklist is provided for the genus, which includes 27 valid New World species, and 44 synonyms.
The Tetragonoderus (Peronoscelis) quadriguttatus assemblage is a postulated monophyletic part of the intersectus complex. This assemblage is characterized against a background that includes review of a classification of the genus and comparison, in the form of a key, to other unrelated Western Hemisphere genera that share elongate tibial spurs with Tetragonoderus Dejean. The principal, easily observed feature that unites the three members (T. laevigatus Chaudoir, 1876; T. deuvei, new species (type locality: Cuijaba, Mato Grosso, Brazil), and T. quadriguttatus Dejean) of the quadriguttatus assemblage is the four-spotted elytra (two spots per elytron). These species are treated in detail, including key, synonymy (as required), comparisons, description (external and male genitalic features), habitat (if known), locality data, and geographical range map. Also, T. subfasciatus Putzeys, 1846, the elytral color pattern of whose members may be confused with the spotted pattern of the quadriguttatus assemblage, is treated similarly. The following new synonymies were established: T. quadriguttatus Dejean 1829 = T. columbicus Steinheil 1875 = T. lacordairei Chaudoir 1876 = T. tetragrammus Chaudoir 1876; and T. laevigatus Chaudoir 1876 = T. chaudoiri Liebke 1928 (replacement name for the junior homonym, T. unicolor Chaudoir, 1876). Lectotypes are designated for T. unicolor Chaudoir, T. lacordairei Chaudoir, and T. subfasciatus Putzeys. A neotype is designated for T. quadriguttatus Dejean. New distribution records in the West Indies for T. quadriguttatus are recorded for the islands of Grand Cayman, Jamaica and Hispaniola. These records may be the result of recent natural overseas dispersal from northern South America, or they may be the result of human-mediated accidental introduction, or a combination of both. The southern Floridian (Nearctic) records for T. laevigatus probably represent a recent accidental introduction through commerce, followed by dispersal through flights of adults.
The genus Efferia Coquillett from the Bahamas, Cayman Islands, Cuba, and Jamaica is reviewed. The fauna now totals 16 species with 6 new species described (Ef. bellardii n. sp., Ef. bromleyi n. sp., Ef. hinei n. sp., Ef. insula n. sp., Ef. pina n. sp., and Ef. vinalensis n. sp.). Cuba has the greatest diversity with 10 species, Jamaica 3, the Bahamas 2, and the Cayman Islands 1. Efferia stylata (Fabricius) is removed from the species list of these West Indian islands. The wings of Ef. caymanensis Scarbrough and Ef. bromleyi, spermathecae of Ef. bromleyi, Ef. cubensis (Bromley), Ef. insula, Ef. nigritarsis (Hine), and terminalia of all species are illustrated. Keys for the identification of the species are provided. Specimens of two additional species from Cuba are in too poor a condition to be described but their terminalia are illustrated and the species are included in the key to the males.
Australophanus, new genus, is described and illustrated for Cryptamorpha redtenbacheri (Reitter). Platamus Erichson is synonymized under Telephanus Erichson, new synonymy. Euplatamus Sharp, new status, replaces Platamus Erichson as the genus name. Type species are designated for Aplatamus Grouvelle and Euplatamus Sharp. Telephanus velox (Haldeman) is synonymized under Telephanus atricapillus Erichson. A diagnosis of the tribe Telephanini, a key to the described telephanine genera of the world is presented, and a phylogeny of the family Silvanidae is proposed.
A preliminary checklist of Calpini is provided, incorporating corrections and changes to publication dates and nomenclature as presented in the checklists of Poole (1989), Fibiger and Lafontaine (2005), and Holloway (2005). Culasta Moore is removed from synonymy with Calyptra Ochsenheimer. Eudocima talboti (Prout) and Graphigona antica Walker are placed in synonymy with E. cajeta (Cramer) and G. regina (Guenée), respectively. Africalpe Krüger, Ferenta Walker, Gonodonta Hübner, Graphigona Walker, Oraesia Guenée, and Tetrisia Walker, are added to the tribe based on shared characters. The genera Cecharismena Möschler, Goniapteryx Perty, Pharga Walker, Phyprosopus Grote, Psammathodoxa Dyar, and Radara Walker are removed and considered incertae sedis. Hemiceratoides and Phyllodes are not considered to be members of Calpini.
Attempts to clarify the identity of obscure New Zealand spider taxa have lead to the conclusion that six species are best treated as nomina dubia [Philodromus rubrofrontus Urquhart 1891 (Philodromidae); Dictyna urquhartii Roewer 1951, (Dictynidae); Linyphia albiapiata Urquhart 1891, Linyphia cruenta Urquhart 1891, Linyphia multicolor Urquhart 1891, Linyphia pellos Urquhart 1891 (Linyphiidae)]. Four species currently listed in Araneus Clerck 1757 (Araneidae) are re-affirmed as synonyms [Araneus lineaacutus (Urquhart 1887) = Zealaranea crassa (Walckenaer 1842), Araneus powelli (Urquhart 1894) = Novaranea laevigata (Urquhart 1891), Araneus sublutius (Urquhart 1892b) = Zealaranea trinotata (Urquhart 1890), Araneus ventricosellus (Roewer 1942) = Eriophora heroine (L. Koch 1871)]. An old record of Araneus brisbanae (L. Koch 1867b) (Araneidae) from New Zealand is a misidentification of Eriophora decorosa Urquhart 1894. The family Philodromidae, the genera Dictyna Sundevall 1833 (Dictynidae) and Linyphia Latreille 1804 (Linyphiidae), as well as Tharpyna munda L. Koch 1875 (Thomisidae) and Araneus brisbanae (Araneidae) are absent from New Zealand.