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562 results for “Bumblebees”
Supplementary material 5 from: Polce C, Maes J, Rotllan-Puig X, Michez D, Castro L, Cederberg B, Dvorak L, Fitzpatrick Ú, Francis F, Neumayer J, Manino A, Paukkunen J, Pawlikowski T, Roberts S, Straka J, Rasmont P (2018) Distribution of bumblebees across Europe. One Ecosystem 3: e28143. https://doi.org/10.3897/oneeco.3.e28143
csv table with values for:
Supplementary material 4 from: Polce C, Maes J, Rotllan-Puig X, Michez D, Castro L, Cederberg B, Dvorak L, Fitzpatrick Ú, Francis F, Neumayer J, Manino A, Paukkunen J, Pawlikowski T, Roberts S, Straka J, Rasmont P (2018) Distribution of bumblebees across Europe. One Ecosystem 3: e28143. https://doi.org/10.3897/oneeco.3.e28143
AUC and model settings
Supplementary material 3 from: Polce C, Maes J, Rotllan-Puig X, Michez D, Castro L, Cederberg B, Dvorak L, Fitzpatrick Ú, Francis F, Neumayer J, Manino A, Paukkunen J, Pawlikowski T, Roberts S, Straka J, Rasmont P (2018) Distribution of bumblebees across Europe. One Ecosystem 3: e28143. https://doi.org/10.3897/oneeco.3.e28143
Table S III.2 Pearson's correlation between all bioclimatic and topographic predictors.
FIGURE 35–37 in Review of some mites (Acari: Laelapidae) associated with ants and bumblebees in Western Siberia, Russia
FIGURE 35–37. Cosmolaelaps siberiensis sp. nov., female. 35, leg II; 36, leg III; 37, leg IV.
Figure 2 in New distributional records of Bumblebees (Hymenoptera: Apidae) from Bangus Valley in North Kashmir of Union territory of Jammu and Kashmir, India
Figure 2. Species distribution of Bumblebees (Hymenoptera: Apidae) from Bangus valley, in North-Kashmir Himalaya of Indian Himalayan Region.
Figure 1 in New distributional records of Bumblebees (Hymenoptera: Apidae) from Bangus Valley in North Kashmir of Union territory of Jammu and Kashmir, India
Figure 1. Map showing the study area for sampling of Bumblebee specimens from Bangus Valley in North Kashmir of Indian Himalayan Region.
Figure 3 in Discovery of a Nearctic vicariant bumblebee (Hymenoptera: Apidae) in Eurasia uncovers secondary trans-Beringian exchanges of insect faunas
Figure 3. Median-joining haplotype networks of the available COI sequences of Bombus balteatus Dahlbom 1832 and B. kirbiellus Curtis 1835 from Chukotka and other areas. The circle size is proportional to the number of available sequences belonging to a certain haplotype (the smallest circle = one sequence). The small red circles indicate hypothetical ancestral haplotypes. Red numbers near branches indicate the number of nucleotide substitutions between haplotypes. The dashed red line shows the species-level boundary.
Dataset for paper "Effects of Heavy Metal Accumulation Mediated by Floral Rewards on Key Stages of Growth and Development of Bumblebees (Bombus terrestris L.)"
Open the record for dataset details and reuse information.
TABLE 1 in A new wave of Mesoamerican bumblebees? Revising the weisi-complex to reject numts and pseudospecies (Apidae: Bombus)
<p><b>TABLE 1.</b> Collections from which material has been examined.</p><table><tbody><tr><th>Abbreviation</th><th>Address</th></tr></tbody><tbody><tr><th>AMNH</th><td>American Museum of Natural History, New York, USA</td></tr><tr><th>BMEC</th><td>Bohart Museum of Entomology, University of California, Davis, California, USA</td></tr><tr><th>CAS</th><td>California Academy of Sciences, San Francisco, California, USA</td></tr><tr><th>CNIN</th><td>Colección Nacional de Insectos, Universidad Nacional Autónoma de México, D.F, México</td></tr><tr><th>ECOAB</th><td>El Colegio de la Frontera Sur, San Cristóbal de Las Casas, Chiapas, México</td></tr><tr><th>EMEC</th><td>Essig Museum Entomological Collection, University of California, Berkeley, California, USA</td></tr><tr><th>INHS</th><td>Illinois Natural History Survey, Champaign, Illinois, USA</td></tr><tr><th>LACM</th><td>Natural History Museum of Los Angeles, Los Angeles, California, USA</td></tr><tr><th>MNHP</th><td>Museum National d’Histoire Naturelle, Paris, France</td></tr><tr><th>MZFC</th><td>Museo de Zoología, Facultad de Ciencia UNAM, D. F. Mexico</td></tr><tr><th>NHMUK</th><td>Natural History Museum, London, UK</td></tr><tr><th>SDEI</th><td>Senckenberg Deutsches Entomologisches Institut, Senckenberg, Germany</td></tr><tr><th>SEMC</th><td>Snow Entomological Museum Collection, Lawrence, Kansas, USA</td></tr><tr><th>UCRC</th><td>University of California Riverside Entomology Research Museum, Riverside, California, USA</td></tr><tr><th>UDLAP</th><td>Universidad de las Américas, Puebla, México</td></tr><tr><th>USDA-ARS</th><td>Bee Biology and Systematics Laboratory, Utah State University, Logan, Utah, USA</td></tr><tr><th>USNM</th><td>United State National Entomological Collection, Washington DC, USA</td></tr><tr><th>VAB</th><td>Van Asperen de Boer, Amsterdam, Netherlands (now in Naturalis)</td></tr><tr><th>ZMHB</th><td>Museum für Naturkunde an der Humboldt-Universität, Berlin, Germany</td></tr><tr><th>ZMUC</th><td>Zoological Museum University of Copenhagen, Denmark</td></tr><tr><th>ZSM</th><td>Zoologische Staatssammlung München, Germany</td></tr></tbody></table>
Linked collectors and determiners for: Early-diverging bumblebees from across the roof of the world: the high-mountain subgenus Mendacibombus revised from species' gene coalescents and morphology (Hymenoptera, Apidae).
Natural history specimen data linked to collectors and determiners held within, "Early-diverging bumblebees from across the roof of the world: the high-mountain subgenus Mendacibombus revised from species' gene coalescents and morphology (Hymenoptera, Apidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/3f8866d2-529e-43ad-b971-29fc52a13858">https://bionomia.net/dataset/3f8866d2-529e-43ad-b971-29fc52a13858</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/3f8866d2-529e-43ad-b971-29fc52a13858">https://gbif.org/dataset/3f8866d2-529e-43ad-b971-29fc52a13858</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Widespread polytypic species or complexes of local species? Revising bumblebees of the subgenus Melanobombus world-wide (Hymenoptera, Apidae, Bombus).
Natural history specimen data linked to collectors and determiners held within, "Widespread polytypic species or complexes of local species? Revising bumblebees of the subgenus Melanobombus world-wide (Hymenoptera, Apidae, Bombus)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/7ca72f76-4fae-4305-8601-4662f4cd2b96">https://bionomia.net/dataset/7ca72f76-4fae-4305-8601-4662f4cd2b96</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/7ca72f76-4fae-4305-8601-4662f4cd2b96">https://gbif.org/dataset/7ca72f76-4fae-4305-8601-4662f4cd2b96</a>. Formatted as a Frictionless Data package.
Data from: Intra-specific differences in cognition: Bumblebee queens learn better than workers
<p><span>Species' cognitive traits are shaped by their ecology, and even within a species, cognition can </span><span><span>reflect the behavioural requirements of individuals with diffferent roles</span></span><span>. Social insects have a number of discrete roles (castes) within a colony, and thus offer a useful system to determine how ecological requirements shape cognition. Bumblebee queens are a critical point in the lifecycle of their colony, since its future success is reliant on a single individual's ability to learn about floral stimuli while finding a suitable nest site; </span><span><span>thus, one might expect particularly adept learning capabilities at this stage</span></span><span>. I compared wild </span><i><span>Bombus vosnesenskii</span></i><span> queens and workers on their ability to learn a colour association and found that queens performed better than workers. In addition, queens of another species, </span><i><span>B. insularis, </span></i><span>a cuckoo species with a different lifecycle but similar requirements at this stage, performed equally well as the non-parasitic queens. To control for differences in foraging experience, I then repeated this comparison with lab-based </span><i><span>B. impatiens</span></i><span>, and found that </span><span><span>unmated</span></span><span> queens performed better than workers. These results add to the body of work on how ecology shapes cognition and opens the door to further research in comparative cognition using wild bees.</span></p>
Figure 1 in Bumblebees of the Azores (Apidae: Bombus)
Figure 1. Islands of the Azores archipelago (Wikimedia Commons).
Figure 4 in In a group of its own? Rediscovery of one of the world's rarest and highest mountain bumblebees, Bombus tanguticus
Figure 4. First label from the queen of Bombus tanguticus in Figure 1.
Figure 1 in Hitchhiking with the Vikings? The anthropogenic bumblebee fauna of Iceland - past and present
Figure 1. Distribution records of bumblebee species in Iceland.
Specialized metabolites in floral resources: effects and detection in buff-tailed bumblebees
<p>The selection of appropriate food resources by bees is a critical aspect for the maintenance of their populations, especially in the current context of global change and pollinator decline. Wild bees have a sophisticated ability to forage selectively on specific resources, and can assess the quality of pollen using contact chemosensory perception (taste). While numerous studies have investigated the detection of pollen macronutrients in bees and their impact on bee health and reproductive success, only a few studies have described the gustatory responses of bees towards specialized metabolites. In addition, these studies mostly focused on the response to nectar and neglected pollen, which is the main food resource for both bee imagines and larvae. Whether bees have the ability to detect specialized toxic metabolites in pollen and then rapidly adapt their foraging behavior to avoid them is very little studied. In this study, we tested whether pollen specialized metabolites affect bumblebees at both the micro-colony and individual levels (<i>i.e. </i>bioassays using supplemented pollen), and whether foragers detect these specialized metabolites and potentially display an avoidance behavior (<i>i.e. </i>preference tests using supplemented syrup). Bumblebees were fed with either amygdalin-, scopolamine- or sinigrin-supplemented pollen diets in ratios that mimic 50%, 100% and 200% of naturally occurring concentrations. We found no effect of these specialized metabolites on resource collection, reproductive success and stress response at the micro-colony level. At the individual level, bumblebees fed on 50%-amygdalin or 50%-scopolamine diets displayed the highest scores for damage to their digestive systems. Interestingly, during the preference tests, the solution with 50%-scopolamine displayed a phagostimulatory activity, whereas solution with 50%-amygdalin had a deterrent effect and could trigger an active avoidance behavior in bumblebees, with a faster proboscis retraction. Our results suggest that regulation of toxin intake is not as well-established and effective as the regulation of nutrient intake in bees. Bees are therefore not equally adapted to all specialized pollen metabolites that they can come into contact with.</p>
Visual Tracking of Entire Bumblebee Colonies Using Novel Pipeline Finds No Evidence of Gut-Brain Axis (Replicates 3, 4)
<p>This archive contains raw data processed from video files taken of bumblebee colonies during replicates 3 and 4 of a study on the effect of the gut microbiome on social behaviour. Files ending with "_raw.csv" contain data on read tags, while ones ending with "_noID.csv" contain data on potential tags. Files are named as follows: R[replicate number][Baseline/Data][Day]R[recording session][HiveID][VideoID]</p>
Fig. 5 in Barcoding cryptic bumblebee taxa: B. lucorum, B. crytarum and B. magnus, a case study (Hymenoptera: Apidae: Bombus)
Fig. 5: Comparison of ABI colour traces of fresh (CRY-09) and 100 year old museum DNA (B. magnus turkestanicus), with two miscoding lesions of type T → C, one marked by Y (mixed bases IUPAC code for T/C) in the ABI output file, and one miscoding lesion of type G → A marked by R (mixed bases IUPAC code for G/A) in the ABI output file.
FIGURE 51. B in The bumblebees of North China (Apidae, Bombus Latreille)
FIGURE 51. B. deuteronymus worker visiting Cirsium leo (Asteraceae) in Gansu (PW).
Figures 1-6 from: Bossert S (2015) Recognition and identification of bumblebee species in the Bombus lucorum-complex (Hymenoptera, Apidae) – A review and outlook. Deutsche Entomologische Zeitschrift 62(1): 19-28. https://doi.org/10.3897/dez.62.9000
Figures 1-6 - Shape of first collar as described in the literature. Head and parts of the mesosoma of the respective species are shown in a lateral view. 1–2. Bombus lucorum; 3–4. Bombus cryptarum; 5–6. Bombus magnus. The drawings were provided by Johann Neumayer and are based on Bertsch et al. (2004).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
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