We describe the nesting biology of Centris (Paracentris) burgdorfi, a solitary bee that nests in sandstone in northeastern Brazil. The nest consists of a shallow tunnel with access to the brood cells. Females of C. burgdorfi made 1–7 brood cells per nest with each cell requiring 2.58 ± 0.40 (X ± SD) days to construct. The average cell-building construction time was longer when compared to other Centris species. Females were larger than males, and this difference was reflected in the size of their respective emergence cells. The temperature within C. burgdorfi nests was lower when compared to ambient temperature. Our study is the first to report the nesting biology of C. burgdorfi. The detailed behavior of the female inside the nest was also described, which is unusual in the study of solitary bee nesting biology.
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Melittological notes from Guatemala (Hymenoptera: Anthophila), 1. New country records for Centris Fabricius (Apidae) and Zikanapis Moure (Colletidae)
Three species of bees (Hymenoptera: Apidae, Colletidae) are newly recorded for Guatemala: Centris obscurior Michener, Centris vidua Mocsáry, and Zikanapis inbio (Michener, Engel and Ayala). We discuss aspects of their biology and circumstances of the collecting events and provide information on their presently known distribution.
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- Award ID(s):
- 2127744
- PAR ID:
- 10512979
- Publisher / Repository:
- Center for Systematic Entomology, Inc.
- Date Published:
- Journal Name:
- Insecta mundi
- ISSN:
- 0749-6737
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Introduction Interest for bee microbiota has recently been rising, alleviating the gap in knowledge in regard to drivers of solitary bee gut microbiota. However, no study has addressed the microbial acquisition routes of tropical solitary bees. For both social and solitary bees, the gut microbiota has several essential roles such as food processing and immune responses. While social bees such as honeybees maintain a constant gut microbiota by direct transmission from individuals of the same hive, solitary bees do not have direct contact between generations. They thus acquire their gut microbiota from the environment and/or the provision of their brood cell. To establish the role of life history in structuring the gut microbiota of solitary bees, we characterized the gut microbiota of Centris decolorata from a beach population in Mayagüez, Puerto Rico. Females provide the initial brood cell provision for the larvae, while males patrol the nest without any contact with it. We hypothesized that this behavior influences their gut microbiota, and that the origin of larval microbiota is from brood cell provisions. Methods We collected samples from adult females and males of C. decolorata ( n = 10 each, n = 20), larvae ( n = 4), and brood cell provisions ( n = 10). For comparison purposes, we also sampled co-occurring female foragers of social Apis mellifera ( n = 6). The samples were dissected, their DNA extracted, and gut microbiota sequenced using 16S rRNA genes. Pollen loads of A. mellifera and C. decolorata were analyzed and interactions between bee species and their plant resources were visualized using a pollination network. Results While we found the gut of A. mellifera contained the same phylotypes previously reported in the literature, we noted that the variability in the gut microbiota of solitary C. decolorata was significantly higher than that of social A. mellifera . Furthermore, the microbiota of adult C. decolorata mostly consisted of acetic acid bacteria whereas that of A. mellifera mostly had lactic acid bacteria. Among C. decolorata , we found significant differences in alpha and beta diversity between adults and their brood cell provisions (Shannon and Chao1 p < 0.05), due to the higher abundance of families such as Rhizobiaceae and Chitinophagaceae in the brood cells, and of Acetobacteraceae in adults. In addition, the pollination network analysis indicated that A. mellifera had a stronger interaction with Byrsonima sp. and a weaker interaction with Combretaceae while interactions between C. decolorata and its plant resources were constant with the null model. Conclusion Our data are consistent with the hypothesis that behavioral differences in brood provisioning between solitary and social bees is a factor leading to relatively high variation in the microbiota of the solitary bee.more » « less
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Abstract Historical data suggest that many bee species have declined in body size. Larger‐bodied bees with narrow phenological and dietary breadth are most prone to declines in body size over time. This may be especially true in solitary, desert‐adapted species that are vulnerable to climate change such as
Centris pallida (Hymenoptera: Apidae). In addition, body size changes in species with size‐linked behaviours could threaten the prevalence of certain behavioural phenotypes long‐term.C. pallida solitary bees are found in the Sonoran Desert. Males use alternative reproductive tactics (ARTs) and are dimorphic in both morphology and behaviour.C. pallida male body size has been studied since the 1970s in the same population. The authors collected body size data in 2022 and combined it with published records from 1974–2022. The authors find a persistent decline in the mean head width of patrolling males, and shifts towards smaller body sizes in the populations of males found foraging and hovering. Both morphs declined in average body size, and the proportion of large‐morph males in the population decreased by 8%. Mating males did not decline in mean body size over the last five decades. The authors discuss hypotheses related to the decline inC. pallida male head width. Finally, the authors advocate forC. pallida as an excellent study system for understanding the stability of ARTs with size‐linked behavioural phenotypes. -
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Incoming solar radiation (wavelengths 290–2500 nm) significantly affects an organism’s thermal balance via radiative heat gain. Species adapted to different environments can differ in solar reflectance profiles. We hypothesized that conspecific individuals using thermally distinct microhabitats to engage in fitness-relevant behaviors would show intraspecific differences in reflectance: we predicted individuals that use hot microclimates (where radiative heat gain represents a greater thermoregulatory challenge) would be more reflective across the entire solar spectrum than those using cooler microclimates. Differences in near-infrared (NIR) reflectance (700–2500 nm) are strongly indicative of thermoregulatory adaptation as, unlike differences in visible reflectance (400–700 nm), they are not perceived by ecological or social partners. We tested these predictions in male
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