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Mittelasien (Kasachstan, Kirgistan, Tadschikistan, Turkmenistan, Usbekistan) ist neben dem Mediterranraum das bedeutendste paläarkische Bienen-Diversitätszentrum (MICHENER 1979). POPOV (1957) schätzt für den Raum 1.200 Arten aus 70 Gattungen, die Gesamtzahl dürfte jedoch bei über 2.000 Arten liegen. Über die innere biogeographische Gliederung der Region und die Lage von Endemiezentren ist bei den Bienen jedoch kaum etwas bekannt (POPOV 1958, MARIKOVSKAYA 1999). Am Beispiel der Seidenbienengattung Colletes, die hier aufgrund ihres Artenreichtums sowie des breiten Spektrums besiedelter Lebensraumtypen und Klimagebiete repräsentativ für andere Bienengruppen behandelt wird, werden Verbreitungsbilder analysiert und Endemiezentren identifiziert. Faunistisches und biogeographisches Arbeiten in Mittelasien ist bis heute ein aufwändiges Unternehmen. Die Größe des Raumes – mit 4 Mio. km² fast halb so groß wie Europa –, die in vielen Regionen unterentwickelte Infrastruktur sowie die in vergangenen und gegenwärtigen bürokratischen Hemmnissen begründete schwierige Zugänglichkeit vieler Gebiete ist ursächlich für den unzureichenden Bearbeitungsstand vieler Taxa. Durch uneinheitliche Transliteration, Schreibfehler bei der Etikettierung und Umbenennung von Orten ist die Identifikation von Fundorten häufig schwierig und in einigen Fällen selbst unter Zuhilfenahme historischen Kartenmaterials unmöglich. Die begrenzte Verfügbarkeit lokalfaunistischer Literatur in deutschen Bibliotheken und die Sprachbarriere bei der Nutzung kyrillisch geschriebener Arbeiten sind ein weiteres Hindernis. Aufgrund dieser Schwierigkeiten und dem daraus resultierenden niedrigen Erfassungsgrad in weiten Teilen Mittelasien haben die hier vorgelegten Ergebnisse vorläufigen Charakter.
Three new species of Eupetersia Blüthgen, 1928 (Hymenoptera, Halictidae) from the Oriental Region
(2012)
Three new species, Eupetersia (Nesoeupetersia) singaporensis sp. nov., collected in a mangrove swamp in Singapore, and Eupetersia (Nesoeupetersia) sabahensis sp. nov., collected in the mountains of Sabah, Borneo, and Eupetersia (Nesoeupetersia) yanegai sp. nov., collected in Thailand, are described. This genus is more diversified in the sub-Saharan region, including Madagascar. The only other Oriental species, E. nathani (Baker, 1974), was described from India and is diagnosed and re-illustrated here.
Members of the genus Centris Fabricius (Hymenoptera: Apoidea: Anthophila) constitute a significant component of the Neotropical (including insular) bee fauna, exhibiting high species richness, a moderate to large body size, and extensive interactions with various important plant groups. Females of most species possess specialized morphology adapted for collecting oils from flowers. This study documents the presence of the genus in Cuba, recognizing six species: C. aethiops Cresson, C. cornuta Cresson, C. fulviventris Cresson, C. poecila Lepeletier, C. taina Genaro and Breto new species, and C. tarsata F. Smith. Detailed information is provided for each species, encompassing a diagnosis, natural history, floral associations, seasonal occurrence, and distribution. Centris taina new species is described from Cuba, based on both sexes, which were previously misidentified as C. versicolor (Fabr.) for females and C. fasciatus F. Smith for males due to sexual dimorphism. Centris tarsata is reported as a new national record for Cuba, possibly introduced by humans from South America and now established and widely distributed across the entire island. A key to differentiate the Cuban species of Centris is presented.
ZooBank registration. urn:lsid:zoobank.org:pub:257916DF-2129-4694-876C-49C858046BF6
The bee fauna of the Greater Puerto Rico area was studied. A review of the previous relevant studies is presented. An annotated catalog and information about the origin and distributional patterns are also provided. Thirty-nine species of bees occur in Puerto Rico and adjacent islands. This fauna is composed of four elements: exclusive Puerto Rican endemics (26.5%); Antillean endemics occurring on multiple islands (76.5%); continental species that have also colonized the Antilles (23.5%); and species introduced through human activity (12.8%). The bee fauna was both low in its diversity and showed the highest level of disharmony in relation to other faunas of the Greater Antilles. A lectotype is here designated for Agapostemon krugii Wolcott, 1936.
Many early taxonomic works on North American bees were published by Europeans using specimens collected in the New World, some with type locations so imprecise that uncertainty on the nomenclatural status remains to this day. Two examples come from Fabricius (1745–1808) who described Andrena virescens Fabricius, 1775 and Apis viridula Fabricius, 1793 from “America” and “Boreal America”, respectively. The former species of Agapostemon Guérin-Méneville, 1844 occurs across most of the United States and southern Canada, the latter presumed an endemic to Cuba. The type materials of these two taxa have never been compared to each other, though a morphology-based phylogenetic analysis placed both in distinct species groups. Here we synonymize Apis viridula under Ag. virescens, thereby making Ag. femoralis (Guérin-Méneville, 1844) available as the name for the Cuban species. A lectotype for Ag. femoralis (the type species for the genus Agapostemon) is hereby designated to stabilize this taxonomy. We also synonymize Ag. obscuratus Cresson, 1869 under Ag. femoralis, suggesting that it represents a dark colour polymorphism. As Ag. cubensis Roberts, 1972 is a junior secondary homonym of Ag. cubensis (Spinola, 1851), we offer Ag. robertsi as a replacement name for the former.
Fourteen new species of the Colletes fasciatus species group are described, all of them endemic to the winter rainfall area in South Africa: C. ascopalis sp. nov. ♀, C. carolinae sp. nov. ♀♂, C. cedarbergensis sp. nov. ♀, C. fabiani sp. nov. ♀♂, C. fuscitergus sp. nov. ♂, C. khoisanorum sp. nov. ♀, C. kogelbergensis sp. nov. ♀♂, C. littoralis sp. nov. ♀, C. longitarsus sp. nov. ♂, C. peerboomi sp. nov. ♀, C. richtersveldensis sp. nov. ♀, C. ruschia sp. nov. ♀♂, C. spinipes sp. nov. ♂, C. troetroeensis sp. nov. ♀. Two species are synonymized based on newly recognized sex associations: C. katharinae Kuhlmann, 2007 syn. nov. is synonymized with C. infracognitus Cockerell, 1937 and C. bokkeveldi Kuhlmann, 2007 syn. nov. with C. zygophyllum Kuhlmann, 2007. The previously unknown female of C. inornatus Cockerell, 1946 is described for the first time and new records of already described species are added. All of the currently known 37 species of the C. fasciatus-group are imaged and included in a key to facilitate their identification.
The South African endemic bee genus Redivivoides Michener, 1981 is revised and redefined. The genus comprises seven species, six of which are described here as new: Redivivoides capensis sp. nov. ♀♂, R. eardleyi sp. nov. ♀, R. kamieskroonensis sp. nov. ♀, R. karooensis sp. nov. ♀♂, R. namaquaensis sp. nov. ♀♂ and R. variabilis sp. nov. ♀♂. A key to species is provided.
The South African endemic bees of the "euryglossiform" species of the genus Scrapter Lepeletier & Serville, 1828 are revised and illustrated. The species-group is defined for the first time and comprises 20 species, 16 of which are described here as new: Scrapter exiguus sp. nov. ♀, ♂, S. gessorum sp. nov. ♀, S. inexpectatus sp. nov. ♀, S. luteistigma sp. nov. ♀, ♂, S. minutissimus sp. nov. ♂, S. minutuloides sp. nov. ♀, S. minutus sp. nov. ♀, S. nanus sp. nov. ♀, ♂, S. nigerrimus sp. nov. ♀, S. nigritarsis sp. nov. ♀, S. papkuilsi sp. nov. ♀, ♂, S. punctatus sp. nov. ♀, ♂, S. pygmaeus sp. nov. ♀, S. roggeveldi sp. nov. ♀, ♂, S. spinipes sp. nov. ♀, ♂ and S. ulrikae sp. nov. ♀, ♂. For S. acanthophorus Davies, 2005 and S. sittybon Davies, 2005 the female is here described for the first time. A key to all species is provided.
The nitidus species group of the bee genus Scrapter Lepeletier & Serville, 1828 is redefi ned, revised and 15 species are described as new for science: S.caeruleus sp. nov. ♀, S.confusus sp. nov. ♀♂, S.convexoides sp. nov. ♂, S. convexus sp. nov. ♀♂, S. crassipunctatus sp. nov. ♀♂, S.felicis sp. nov. ♀♂, S.fl avipunctatus sp. nov. ♀♂, S.imparilis sp. nov. ♀♂, S. littoralis sp. nov. ♀, S.longicornis sp. nov. ♂, S.montanus sp. nov. ♀♂, S.mpumalangensis sp. nov. ♀♂, S.obtusus sp. nov. ♀♂, S. perpunctatulus sp. nov. ♂ and S.variabilis sp. nov. ♀♂. The previously unknown males of S. divergens (Friese, 1925), S. semirufus Cockerell, 1932 and S. perpunctatus Cockerell, 1933 are described for the fi rst time. All currently known 28 species of the S. nitidus species group are redescribed, imaged and included in a key to facilitate their identifi cation.
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 %).