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Revision of the genus Paramecocephala Benvegnú, 1968 (Heteroptera, Pentatomidae). The Neotropical genus Paramecocephala Benvegnú, 1968 is revised based on morphological characters, particularly of the genitalia of both sexes. Formerly monobasic with P. foveata Benvegnú, 1968, type species, the genus received two species recently transferred from Mecocephala Dallas, 1851: M. fusca Haglund, 1868 and M. uruguayensis Pirán, 1970. Five new species are herein described: P. australis Frey-da-Silva & Grazia sp. nov., P. bachmanni Frey-da-Silva & Grazia sp. nov., P. bergrothi Frey-da-Silva & Grazia sp. nov., P. guianensis Frey-da-Silva & Grazia sp. nov. and P. subsolana Frey-da-Silva & Grazia sp. nov. Illustrations of the genitalia, a key to the species and a distribution map are provided.

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The genus Anthidium Fabricius in the South America: key for the species, descriptive notes, and geographical distribution (Hymenoptera, Megachilidae, Anthidiini). The Anthidiini, in South America, is represented by a single genus Anthidium Fabricius, 1804 (type-species: Apis manicata Linnaeus, 1758). Thirty nine species are treated in this paper, as follows: Anthidium alsinai Urban, 2001; A. andinum Joergensen, 1912; A. anurospilum Moure, 1957 nom. reval. (formerly = A. espinosai Ruiz, 1938); A. atricaudum Cockerell, 1926; A. aymara Toro & Rodríguez, 1998; A. chilense Spinola, 1851; A. chubuti Cockerell, 1910; A. colliguayanum Toro & Rojas, 1970; A. cuzcoense Schrottky, 1910; A. danieli Urban, 2001; A. decaspilum Moure, 1957; A. deceptum Smith, 1879; A. edwini Ruiz, 1935; A. espinosai Ruiz, 1938; A. falsificum Moure, 1957; A. friesei Cockerell, 1911; A. funereum Schletterer, 1890; A. garleppi Schrottky, 1910 = A. matucanense Cockerell, 1914 syn. nov.; A. gayi Spinola, 1851; A. igori Urban, 2001; A. larocai Urban, 1997; A. latum Schrottky, 1902; A. luizae Urban, 2001; A. manicatum (Linnaeus, 1758); A. masunariae Urban, 2001; A. nigerrimum Schrottky, 1910; A. paitense Cockerell, 1926; A. penai Moure, 1957; A. peruvianum Schrottky, 1910; A. rafaeli Urban, 2001; A. rozeni Urban, 2001; A. rubripes Friese, 1908 = A. boliviense Friese, 1920 syn. nov. = A. adriani Ruiz, 1935 syn. nov. = A. kuscheli Moure, 1957 syn. nov.; A. sanguinicaudum Schwarz, 1933; A. sertanicola Moure & Urban, 1964; A. tarsoi Urban, 2001; A. toro Urban. 2001; A. vigintiduopunctatum Friese, 1904; A. vigintipunctatum Friese, 1908, and A. weyrauchi Schwarz, 1943. Some taxonomic comments are made for each species, and new data on geographic distribution are also given. The females of A. andinum, A. igori, A. rozeni and the male of A. anurospilum are described for the first time. Identification keys (for males and females), as well as illustrations for almost all species, are provided.

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Redescription and transference of the genus Fregolia Gounelle, 1911 to Callidiopini (Coleoptera, Cerambycidae). The genus Fregolia is transferred from Cleomenini Lacordaire, 1869 to Callidiopini Lacordaire, 1869. The genus and its type species, Fregolia listropteroides Gounelle, 1911, the only known species to the genus, are redescribed including characters of the mouth pieces, endosternites, wing venation, and male and female terminalia.

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Synopsis of the genus Strongylaspis Thomson, 1860 (Coleoptera, Cerambycidae, Prioninae, Macrotomini). The genus Strongylaspis Thomson, 1860 with its twelve known species are briefly treated herein: S. batesi Lameere, 1903, S. bullatus Bates, 1872, S. championi Bates, 1884, S. corticarius (Erichson, 1848), S. dohrni Lameere, 1903, S. fryi Lameere, 1912, S. graniger Bates, 1884, S. hirticollis Tippmann, 1953, S. kraepelini Lameere, 1903, S. macrotomoides Tippmann, 1953, S. sericans Tippmann, 1953, S. sericeus Zajciw, 1970. The genus as well as the species, Strongylaspis championi, S. bullatus and S. corticarius are redescribed; the last one including characterization of wings and male and female terminalia. Four new species are added: S. aureus sp. nov. (BRASIL, Amazonas), S. migueli sp. nov. (BRASIL, Mato Grosso), S. christianae sp. nov. (BRASIL, Mato Grosso) and S. bolivianus sp. nov. (BOLIVIA). All the species, but S. dohrni, are illustrated and keyed. Maps of distribution are also given.

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The genus Xylocopa Latreille in Rio Grande do Sul, Brazil (Hymenoptera, Anthophoridae). A survey of the genus Xylocopa Latreille, 1802 is given for Rio Grande do Sul, the southernmost State of Brazil. Data are based on several studies on the bee fauna of southern Brazil and on unpublished observations. A key is provided to the species (males and females) and information on distribution, nesting habits and relation to flowers. Rio Grande do Sul is strikingly rich in species of Xylocopa because of the diversity of habitats and its geographic position in the transition of tropical/subtropical to temperate climate. Nineteen species, classified into ten subgenera, have been recorded in Rio Grande do Sul. Here we maintain the subgenera Ioxylocopa, Megaxylocopa and Xylocospila, which were put into synonymy recently by Minckley (1998). The species are: Xylocopa (Dasyxylocopa) bimaculata Friese, 1903; Xylocopa (Ioxylocopa) chrysopoda Schrottky, 1902; Xylocopa (Megaxylocopa) frontalis (Olivier, 1789); Xylocopa (Nanoxylocopa) ciliata Burmeister, 1876; Xylocopa (Neoxylocopa) augusti Lepeletier, 1841; Xylocopa (N.) brasilianorum (Linnaeus, 1767); Xylocopa (N.) haematospila Moure, 1951; Xylocopa (N.) hirsutissima Maidl, 1912; Xylocopa (N.) nigrocincta Smith, 1854; Xylocopa (N.) ordinaria Smith, 1874; Xylocopa (N.) suspecta Moure & Camargo, 1988; Xylocopa (N.) tacanensis Moure, 1949; Xylocopa (Schonnherria) macrops Lepeletier, 1841; Xylocopa (S.) simillima Smith, 1854; Xylocopa (S.) splendidula Lepeletier, 1841; Xylocopa (S.) varians Smith, 1874; Xylocopa (Stenoxylocopa) artifex Smith, 1874; Xylocopa (Xylocopoda) elegans Hurd & Moure, 1963; Xylocopa (Xylocopsis) funesta Maidl, 1912; Xylocopa (Xylocospila) bambusae Schrottky, 1902. Xylocopa tacanensis is for the first time recorded in Brasil.

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Synopsis of the genus Phacellocerina Lane, 1964 (Coleoptera, Cerambycidae, Lamiinae, Anisocerini). The genus Phacellocerina Lane, 1964 and P. limosa (Bates, 1862) (type species) are redescribed; P. silvanae sp. nov. is described from Colombia (Santa Marta). A key to the species is added.

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The genus Anisocerus and the two species, A. scopifer (Germar, 1824) and A. stellatus Guérin-Ménéville, 1855, are redescribed and illustrated. A new synonym is proposed: A. stellatus Guérin-Méneville, 1855 = A. onca White, 1855 syn. nov. The two species are redescribed and illustrated.

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Unanthribus gen. nov. is proposed to include Unanthribus maximus sp. nov. (type species) described from Brazil (Pará), and U. grandis (Jordan, 1911) comb. nov., which is redescribed. The species are illustrated and keyed.

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The genus Physopleurus Lacordaire, 1869 = Basitoxus (Parabasitoxus) Fragoso & Monné, 1995 syn. nov. is revised and redefined based on new characters. The following species are treated (in sequence that appear in the presented key): Physopleurus exiguus sp. nov. (Bolivia and Brazil), P. crassidens (Bates, 1869), P. longiscapus Lameere, 1912, P. rugosus (Gahan, 1894), P. tritomicros Lameere, 1912, P. seripierriae sp. nov. (Brazil, Mato Grosso), P. dohrnii Lacordaire, 1869, P. villardi (Lameere, 1902) = Aplagiognathus guatemalensis Casey, 1912 syn. nov., P. amazonicus (Fragoso & Monné, 1995) comb. nov., and. P. maillei (Audinet-Serville, 1832) comb. nov. The latter two species formerly in Basitoxus (Parabasitoxus) Fragoso & Monné, 1995. Illustrations of Basitoxus megacephalus (Germar, 1824) are included to allow comparisons with Physopleurus species. Key to species of Physopleurus is added.

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This work, dedicated to the study of nesting habits of the species of the Neotropical genus Partamona Schwarz, is a sequence to the taxonomic revision recently published elsewhere. A total of 214 nests and nest aggregations of 18 species [Partamona epiphytophila Pedro & Camargo, 2003; P. testacea (Klug, 1807); P. mourei Camargo, 1980; P. vicina Camargo, 1980; P. auripennis Pedro & Camargo, 2003; P. combinata Pedro & Camargo, 2003; P. chapadicola Pedro & Camargo, 2003; P. nhambiquara Pedro & Camargo, 2003; P. ferreirai Pedro & Camargo, 2003; P. pearsoni (Schwarz, 1938); P. gregaria Pedro & Camargo, 2003; P. batesi Pedro & Camargo, 2003; P. ailyae Camargo, 1980; P. cupira (Smith, 1863); P. mulata Moure in Camargo, 1980; P. seridoensis Pedro & Camargo, 2003; P. criptica Pedro & Camargo, 2003; P. helleri (Friese, 1900)] were studied , including data about habitat, substrate, structural characteristics, construction materials and behavior. The descriptions of the nests are illustrated with 48 drawings. Partial data of the nests of P. bilineata (Say, 1837), P. xanthogastra Pedro & Camargo, 1997, P. orizabaensis (Strand, 1919), P. peckolti (Friese, 1901), P. aequatoriana Camargo, 1980, P. musarum (Cockerell, 1917) and P. rustica Pedro & Camargo, 2003 are also presented. Nests of P. grandipennis (Schwarz, 1951), P. yungarum Pedro & Camargo, 2003, P. subtilis Pedro & Camargo, 2003, P. vitae Pedro & Camargo, 2003, P. nigrior (Cockerell, 1925), P. sooretamae Pedro & Camargo, 2003 and P. littoralis Pedro & Camargo, 2003 are unknown. The species of Partamona build notable nest entrance structures, with special surfaces for incoming / exiting bees; some of them are extremely well-elaborated and ornamented, serving as flight orientation targets. All species endemic to western Ecuador to Mexico with known nesting habits (P. orizabaensis, P. peckolti, P. xanthogastra, P. bilineata, P. aequatoriana and P. musarum) build their nests in several substrates, non-associated with termitaria, such as cavities and crevices in walls, among roots of epiphytes and in bases of palm leaves, in abandoned bird nests, under bridges, and in other protected places, except P. peckolti that occasionally occupies termite nests. In South America, on the eastern side of the Andes, only P. epiphytophila and P. helleri nest among roots of epiphytes and other substrates, non-associated with termitaria. All other species studied (P. batesi, P. gregaria, P. pearsoni, P. ferreirai, P. chapadicola, P. nhambiquara, P. vicina, P. mourei, P. auripennis, P. combinata, P. cupira, P. mulata, P. ailyae, P. seridoensis, P. criptica and P. rustica) nest inside active termite nests, whether epigeous or arboreous. The only species that builds obligate subterranean nests, associated or not with termite or ant nests (Atta spp.) is P. testacea. Nests of Partamona have one vestibular chamber (autapomorphic for the genus) closely adjacent to the entrance, filled with a labyrinth of anastomosing pillars and connectives, made of earth and resins. One principal chamber exists for food and brood, but in some species one or more additional chambers are filled with food storage pots. In nests of P. vicina, there is one atrium or "false nest", between the vestibule and the brood chamber, which contains involucral sheaths, cells and empty pots. All structures of the nest are supported by permanent pillars made of earth and resins (another autapomorphy of the genus). The characters concerning nesting habits were coded and combined with morphological and biogeographic data, in order to hypothesize the evolutive scenario of the genus using cladistic methodology. The phylogenetic hypothesis presented is the following: (((((P. bilineata (P. grandipennis, P. xanthogastra)) (P. orizabaensis, P. peckolti)) (P. aequatoriana, P. musarum)) P. epiphytophila, P. yungarum, P. subtilis, P. vitae) (((((P. testacea (P. mourei, P. vicina)) (P. nigrior (P. auripennis, P. combinata))) (P. ferreirai (P. pearsoni (P. gregaria (P. batesi (P. chapadicola, P. nhambiquara)))))) ((((P. ailyae, P. sooretamae) P. cupira, P. mulata) P. seridoensis) P. criptica, P. rustica, P. littoralis)) P. helleri))). One area cladogram is presented. Dates of some vicariance / cladogenesis events are suggested. For bilineata / epiphytophila group, which inhabits the Southwestern Amazonia and the Chocó-Mexican biogeographical components, the origin of ancestral species is attributed to the Middle Miocene, when the transgressions of the Maracaibo and Paranense seas isolated the tropical northwestern South America from the eastern continental land mass. The next cladogenic event in the history of the bilineata / epiphytophila group is attributed to the Plio-Pleistocene, when the Ecuadorian Andes reached more than 3000 m, and the ancestral species was fragmented in two populations, one occupying the western Andes (ancestral species of the bilineata subgroup) and other the southwestern Amazon (ancestral species of the epiphytophila subgroup). Other aspects of the history of Partamona are also discussed.

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Neotropical Meliponini: the genus Partamona Schwarz, 1939 (Hymenoptera, Apidae). The systematics and biogeography of Partamona Schwarz, a Neotropical genus of stingless bees (Meliponini, Apinae, Apidae), are revised. Seventeen new species are described: P. epiphytophila sp. nov., P. subtilis sp. nov., P. nhambiquara sp. nov., P. batesi sp. nov., P. yungarum sp. nov., P. vitae sp. nov., P. ferreirai sp. nov., P. gregaria sp. nov., P. auripennis sp. nov., P. nigrilabris sp. nov., P. combinata sp. nov., P. chapadicola sp. nov., P. seridoensis sp. nov., P. littoralis sp. nov., P. criptica sp. nov., P. rustica sp. nov. and P. sooretamae sp. nov. Partamona pseudomusarum Camargo, 1980, is considered as junior synonym of P. vicina Camargo, 1980. Types of P. grandipennis (Schwarz, 1951), P. xanthogastra Pedro & Camargo, 1996-1997, P. pearsoni (Schwarz, 1938), P. ailyae Camargo, 1980, P. pseudomusarum, P. vicina, P. mulata Moure in Camargo, 1980, P. aequatoriana Camargo, 1980, P. mourei Camargo, 1980, P. peckolti, (Friese, 1901), P. testacea (Klug, 1807), P. helleri (Friese, 1900) and P. musarum (Cockerell, 1917) were examined. Lectotypes of P. orizabaensis (Strand, 1919), and P. cupira (Smith, 1863) are designated. An identification key for the species and drawings of morphological characters are presented. A phylogenetic hypothesis, based mainly on morphological characters is proposed. Four groups are defined, considering the shape of mandible of workers and sternum VII of males: bilineata / epiphytophila group (western Amazon to México), including P. bilineata (Say), P. grandipennis, P. xanthogastra P. orizabaensis P. peckolti P. epiphytophila sp. nov., P. subtilis sp. nov., P. nhambiquara sp. nov., P. batesi sp. nov., P. yungarum sp. nov. and P. vitae sp. nov.; musarum group (Central Brazil, north of South America to Central America), including P. musarum, P. aequatoriana, P. vicina, P. mourei, P. pearsoni, P. ferreirai sp. nov., P. gregaria sp. nov. and P. testacea; nigrior group (Central Brazil to northeast of South America) including P. nigrior (Cockerell, 1925), P. auripennis sp. nov., P. nigrilabris sp. nov., P. combinata sp. nov., P. chapadicola sp. nov., P. seridoensis sp. nov. and P. littoralis sp. nov., and cupira group (southeastern and Central Brazil), including P. cupira, P. mulata, P. ailyae, P. sooretamae sp. nov., P. criptica sp. nov., P. rustica sp. nov. and P. helleri. Some geographic distribution patterns, congruent with that of other Meliponini bees, are commented.

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O gênero Beloesthes Thomson, 1864 e B. megabasoides Thomson, 1864 são redescritos e figurados. Alcathousites asperipennis (Fairmaire & Germain, 1859) comb. nov. (antes em Leiopus) = Alcathousites chaclacayoi Gilmour, 1962 syn. nov.

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O gênero Lophyraspis e as seguintes espécies, juntamente com algumas mudanças nomenclaturais, são tratados: Lophyraspis Stål, 1869 = Gerridius Fowler, 1896 syn. rest.; Lophyraspis muscaria (Fabricius, 1803) = Gerridius scutellatus Fowler, 1896 syn. nov. = Gerridius abbreviatus Baker, 1907 syn. nov.; Lophyraspis pygmaea (Fabricius, 1803); Lophyraspis scutellata (Fabricius, 1803) = L. cristata Stål, 1869 syn. nov. = L. armata Haviland, 1925 syn. nov.; Lophyraspis spinosa (Funkhouser, 1930) comb. nov. (anteriormente em Mina Walker, 1858); Lophyraspis fenestrata sp. nov. (Brasil, Amazonas); Lophyraspis diminuta sp. nov. (Brasil, Mato Grosso).