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Made available in DSpace on 2022-04-28T17:21:54Z (GMT). No. of bitstreams: 0 Previous issue date: 2022-04-05 Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) National Science Foundation (NSF) U.S. Department of Agriculture (USDA) Fundacao de Apoio a Pesquisa do Distrito Federal (FAPDF) Aim An antitropical pattern is characterized by the occurrence of closely related taxa south and north of the tropics but absent or uncommonly represented closer to the equator, in contrast to most taxa, which tend to have their highest diversity in the tropical regions. We investigate the antitropical distribution of eucerine bees with the aim of contributing to the characterization and understanding of this pattern. Location All continents except Antarctica and Australia. Taxon Eucerine bees (Hymenoptera: Apidae: Eucerinae). Methods We carried out phylogenomic dating under two different clock models and used multiple strategies to vary matrix composition, evaluating the overlapping of divergence times estimated across models using Bhattacharyya coefficients. Lastly, we reconstructed the biogeographic history of eucerine bees using a Bayesian implementation of the DEC model. Results Eucerinae is estimated to have started diversifying during the Palaeocene, with all its tribes originating during the Palaeocene/Eocene transition in southern South America. At least two range expansions happened into North America before the full closure of the Isthmus of Panama. We show that divergence between closely related groups with disjunct distributions would have happened in periods when the climate favoured the expansion of open habitats and became isolated when the forests were re-established. Main conclusions We describe the early diversification of eucerine bees, revealing an intimate association with southern South America. Events of range evolution of Eucerinae were likely affected by periods of global cooling and aridification, and palaeoclimatic and vegetational conditions probably have been more relevant to the formation of the antitropical distribution of Eucerinae than the consolidation of the Isthmus of Panama connecting the Americas. We also demonstrate that most uncertainty in divergence time estimation is not due to the amount of molecular data being used, but more likely other factors like fossil calibrations and violations of clock models. Univ Sao Paulo, Fac Filosofia Ciencias & Letras, Dept Biol, Lab Biol Comparada & Abelhas LBCA, Ribeirao Preto, Brazil Utah State Univ, USDA ARS, Pollinating Insects Res Unit, Logan, UT 84322 USA Univ Fed Minas Gerais, Dept Zool, Lab Evolucao Mamiferos, Belo Horizonte, MG, Brazil Univ Brasilia, Dept Zool, Lab Abelhas, Brasilia, DF, Brazil

Gynandromorphs are individuals that exhibit aspects of both males and females simultaneously and are the most commonly reported sexual anomalies in bees. We describe the first known specimen of a gynandromorph of the specialist pollinator Florilegus condignus (Cresson, 1878) (Hymenoptera: Apidae: Eucerini) collected in an agricultural field in northwestern Mississippi, USA. Additionally, we include and discuss phenological data from collections made in Mississippi and the Mid-Atlantic region of the United States.

Sex‐associated differences in behavior can have large ecological consequences, especially in plant–pollinator communities where floral visitor behavior affects plant reproduction. Whether these differences are prevalent enough to impact community‐level processes, however, is unknown. Using 256 plant–pollinator communities, we built networks where the floral interactions of each sex were modeled separately, comparing observations to simulated networks where sex was randomized. We found that (1) in many species the sexes differed in their network roles and visited different partners, with females tending to visit more species and more peripheral species than males; (2) more generalist species differed more in network roles between the sexes; and (3) networks where nodes were separated by sex were more specialized than simulated networks, but were similarly resistant to perturbations. These findings suggest that despite variation among species, sex‐associated differences in behavior are large enough to impact the network roles of male and female pollinators and common enough to influence the interaction patterns of entire plant–pollinator communities.

Efforts to understand activity patterns of bees, our most important pollinators, often rely on opportunistically collected museum records to model temporal shifts or declines. This type of data, however, may not be suitable for this purpose given high spatiotemporal variability of native bee activity. By comparing phenological metrics calculated from intensive systematic inventory data with those from opportunistic museum records for bee species spanning a range of functional traits, we explored biases and limitations of data types to determine best practices for bee monitoring and assessment. We compiled half a million records of wild bee occurrence from opportunistic museum collections and six systematic inventory efforts, focusing analyses on 45 well-represented species that spanned five functional traits: sociality, nesting habits, floral specialization, voltinism, and body size. We then used permutation tests to evaluate differences between data types in estimating three phenology metrics: flight duration, number of annual abundance peaks, and date of the highest peak. We used GLMs to test for patterns of data type significance across traits. All 45 species differed significantly in the value of at least one phenology metric depending on the data type used. The date of the highest abundance peak differed for 40 species, flight duration for 34 species, and the number of peaks for 15 species. The number of peaks was more likely to differ between data types for larger bees, and flight duration was more likely to differ for larger bees and specialist bees. Our results reveal a strong influence of data type on phenology metrics that necessitates consideration of data source when evaluating changes in phenological activity, possibly applicable to many taxa. Accurately assessing phenological change may require expanding wild bee monitoring and data sharing.

A systematic study of Perdita subgenus Procockerellia Timberlake and the related subgenus Allomacrotera Timberlake results in the synonymy of the latter with the former, and two specific synonymies: Perdita (Hexaperdita) glamis Timberlake is a junior synonym of Perdita (Procockerellia) stephanomeriae Timberlake, while Perdita (Procockerellia) brachyglossa Timberlake is a junior synonym of Perdita (Cockerellia) imbellis Timberlake. Perdita (Procockerellia) moldenkei Timberlake is moved to subgenus Cockerellia Ashmead. A revised subgeneric diagnosis and key to the three included species are provided. Diagnoses of species are updated with novel characters; distributions and biological data are expanded. A gynandromorph of P. (Procockerellia) moabensis Timberlake, the first known in the genus Perdita, is reported.

Perdita subgenus Heteroperdita Timberlake, a distinctive subgenus of 22 species from the southwestern United States and adjacent Mexico, all specialists on Tiquilia (Boraginaceae), is revised. Nine new species are described: Perdita (Heteroperdita) desdemona Portman, sp. n., P. (H.) exusta PortmanGriswold, sp. n., P. (H.) hippolyta PortmanGriswold, sp. n. (male previously incorrectly described as P. pilonotata Timberlake), P. (H.) hooki PortmanNeff, sp. n., P. (H.) nuttalliae Portman, sp. n., P. (H.) prodigiosa PortmanGriswold, sp. n., P. (H.) sycorax Portman, sp. n., P. (H.) titania PortmanGriswold, sp. n., and P. (H.) yanegai Portman, sp. n. The following sexes are associated and described for the first time: the male of P. (H.) frontalis Timberlake, 1968, the female of P. (H.) optiva Timberlake, 1954, and the true male of P. (H.) pilonotata Timberlake, 1980. Perdita (H.) fasciatella Timberlake, 1980 is proposed as a junior synonym of P. (H.) sexfasciata Timberlake, 1954. A neotype is designated for P. (H.) pilonotata Timberlake, 1980. Two species in particular, P. prodigiosa and P. pilonotata, are sexually dimorphic with distinctive ant-like males. Information is presented on floral relationships, phenology, and geographic distribution. Identification keys for males and females are provided.

The resin bees of the genus Anthidiellum Cockerell, 1904 are revised for China. Seven species are confirmed to occur in China including five new combinations: A. (Pycnanthidium) carinatum (Wu, 1962) comb. nov., A. (P.) coronum (Wu, 2004a) comb. nov., A. (P.) latipes (Bingham, 1897) comb. nov., A. (Clypanthidium) popovii (Wu, 1962) comb. nov., and A. (Anthidiellum) yunnanensis (Wu, 1962) comb. nov.. These five species had previously been classified as Trachusa (Paraanthidium), which is characterized by much larger-bodied bees (only four species of Trachusa (Paraanthidium) are confirmed to occur in China after this study; others reported in the literature were misplaced to genus). Additionally, Anthidiellum ludingensis Wu, 1993, and Anthidiellum (Anthidiellum) xinjiangensis Wu, 2004b, are removed from Anthidiellum forming the new combinations Pseudoanthidium (Pseudoanthidium) ludingense (Wu, 1993) and P. (P.) xinjiangense (Wu, 2004b), thus extending the range of the genus in China to include Sichuan. Illustrations and a key to known Chinese Anthidiellum species are provided.

The Sub-Saharan bee genus Serapista Cockerell is revised. It comprises six species. Serapista pernigra Cockerell is restored as a valid species, S. aspernigra Eardley and Griswold, new species, is described from the eastern part of southern Africa and Serapista rhodesiana Mavromoustakis is synonymized with S. pernigra. Descriptions, keys for identification, distributional records and floral associations of the species of Serapista are given.

The monotypic Perdita subgenus Xeromacrotera Timberlake is currently known only from the male sex. Here, the female of Perdita (Xeromacrotera) cephalotes (Cresson, 1878) is associated, resulting in two new junior synonyms of P. (X.) cephalotes: Perdita (Procockerellia) excellens Timberlake, 1958, new synonym and Perdita (Cockerellia) autumnalis Timberlake, 1977, new synonym. The true number of maxillary palpi are reported, and updated subgeneric and species diagnoses are provided. In addition, Perdita boharti PortmanGriswold, new name, is designated as a replacement name for the primary junior homonym P. bohartorum Parker, 1983 (not P. bohartorum Timberlake, 1956) and is assigned to the related subgenus Cockerellia Ashmead.

Two new species of squash bees, Peponapis pacifica Ayala and Griswold sp. n. and P. parkeri Griswold and Ayala sp. n., are described and illustrated. Peponapis pacifica is oligolectic on flowers of Schizocarpum longisepalum (Cucurbitaceae) endemic to Mexico, where it is found in the tropical dry forest along the Pacific Coast, between Sonora and Chiapas and in the Balsas River basin; and P. parkeri is known only from the Pacific slope of Costa Rica. A key for the North and Central American species of Peponapis is provided.Se describen e ilustran 2 especies nuevas de abejas, Peponapis pacifica Ayala and Griswold sp. n. y P. parkeri Griswold and Ayala sp. n. De éstas, P. pacifica es oligoléctica sobre flores de Schizocarpum longisepalum (Cucurbitaceae), endémica de México, con distribución asociada al bosque tropical caducifolio a lo largo de la vertiente del Pacífico entre Sonora y Chiapas y en la Cuenca del río Balsas; P. parkeri es conocida sólo para la vertiente del Pacífico de Costa Rica. Se incluye una clave para las especies de América del norte y central.

Descriptions and diagnoses of ten new Nearctic species of Stelis subgenus Stelis are presented: S. alta, S. anasazi, S. anthocopae, S. broemelingi, S. imperialis, S. joanae, S. lamelliterga, S. occidentalis, S. paiute, and S. shoshone. Six of these species have been reared from trapnests. Host associations, all within the tribe Osmiini (Megachilidae), are provided.

The southern African bee genus Plesianthidium Cameron is revised. It comprises twelve species. Two new species are described: Plesianthidium (Spinanthidium) richtersveldense sp. nov. (Namibia and South Africa) and P. (S.) namaquaense sp. nov. (South Africa). Two species, Plesianthidium calvini (Cockerell, 1932) and P. rufocaudatum (Friese, 1909), are reinstated as valid species. Keys for the identification of the species of Plesianthidium are given.

The orchid bee genus Eufriesea Cockerell is documented for the first time from the southwestern United States, extending its apparent range north well beyond its previous tropical/subtropical boundaries. Eufriesea coerulescens (Lepeletier de Saint Fargeau 1841) is recorded from the Guadalupe Mountains of western Texas and southeastern New Mexico, USA. Whether E. coerulescens is resident in the USA, or merely a vagrant from Mexico, remains unclear. Distinctive morphological traits shared with the holotype are enumerated and illustrated. In addition, observations that question the current species concept and distribution of E. coerulescens are provided.

The rare genus Trachusoides, previously known only from a single species inhabiting the Western Ghats of India, is reviewed. Trachusoides elsieae, new species, is described from Laos, additional records for T. simplex are documented, and a key to separate the species is provided.

Griswold, Terry, Miller, Wensdae (2010): A Revision of Perdita (Xerophasma) Timberlake (Hymenoptera: Andrenidae). Zootaxa 2517 (1): 1-14, DOI: 10.11646/zootaxa.2517.1.1, URL: https://biotaxa.org/Zootaxa/article/view/zootaxa.2517.1.1

"Two new species of squash bees, Peponapis pacifica Ayala and Griswold sp. n. and P. parkeri Griswold and Ayala sp. n., are described and illustrated. Peponapis pacifica is oligolectic on flowers of Schizocarpum longisepalum (Cucurbitaceae) endemic to Mexico, where it is found in the tropical dry forest along the Pacific Coast, between Sonora and Chiapas and in the Balsas River basin; and P. parkeri is known only from the Pacific slope of Costa Rica. A key for the North and Central American species of Peponapis is provided."