Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
6
datasets available to search
ShareScore release 0.9.0
Dataset results
6 results for “Xylophanes”
FIGURES 8–12 in Morphology and DNA barcoding reveal three cryptic species within the Xylophanes neoptolemus and loelia species-groups (Lepidoptera: Sphingidae)
FIGURES 8–12. Drawings of diagnostic details of the male genitalia of Xylophanes loelia (Figs. 8a–c), X. lolita n. sp. (Figs. 9a–c), X. neoptolemus (Figs. 10a–c), X. balcazari n. sp. (Figs. 11a–c), and X. cthulhu n. sp. (Figs. 12a–c); a. uncus in lateral view, b. harpe, c. posterior end of the aedeagus.
FIGURES 1–4. 1a in Morphology and DNA barcoding reveal three cryptic species within the Xylophanes neoptolemus and loelia species-groups (Lepidoptera: Sphingidae)
FIGURES 1–4. 1a. Chaerocampa trilineata Walker, [1865], Lectotype, ♂, Venezuela; 1b. Watercolour of the original type of Sphinx neoptolemus Cramer, 1780; 2a and 2b. Xylophanes balcazari n. sp., Holotype, ♂, Mexico, Guerrero; 3a and 3b. Sphinx neoptolemus, Neotype, ♂, Venezuela, Aragua; 4a and 4b. Xylophanes cthulhu n. sp., Holotype, ♂, Guatemala, Izabal. (2a, 3a, 4a: dorsal view; 2b, 3b, 4b: ventral view).
FIGURE 13 in Morphology and DNA barcoding reveal three cryptic species within the Xylophanes neoptolemus and loelia species-groups (Lepidoptera: Sphingidae)
FIGURE 13. Strict consensus of the nine equally most-parsimonious cladograms (length=133, CI=0.78, RI=0.94) resulting from the phylogenetic analysis of the complete dataset of DNA barcode sequences for 38 specimens belonging to the Xylophanes neoptolemus (yellow) and X. loelia (blue) species complexes (X. cyrene, X. aglaor and X. libya are outgroup taxa). Each specimen is identified by its SampleID code (see Table 1), and the two specimens with short sequences are highlighted in boxes. The branch lengths are proportional to the number of changes (indicated on branches, optimized under FAST optimization); Bremer support and rescaled Bremer support values are given above the branches for each node, and bootstrap support values are indicated below. Clades within the X. neoptolemus complex are named after groups 1, 2 and 3 as described in the text.
FIGURES 5–7. 5a and 5b. Xylophanes lolita n in Morphology and DNA barcoding reveal three cryptic species within the Xylophanes neoptolemus and loelia species-groups (Lepidoptera: Sphingidae)
FIGURES 5–7. 5a and 5b. Xylophanes lolita n. sp., Holotype, ♂, Brazil, Minas Gerais; 6a and 6b. Chaerocampa loelia Druce, 1878, Lectotype, ♂, Panama, Chiriquí; 7a. Xylophanes heinrichi Closs, 1917, Holotype, ♂ "Amazonas". (5a, 6a, 7a: dorsal view; 5b, 6b: ventral view).
Data from: A diversification relay race from Caribbean-Mesoamerica to the Andes: historical biogeography of Xylophanes hawkmoths
<p>The regions of the Andes and Caribbean-Mesoamerica are both hypothesized to be the cradle for many Neotropical lineages, but few studies have fully investigated the dynamics and interactions between Neotropical bioregions. The NewWorld hawkmoth genus Xylophanes is the most taxonomically diverse genus in the Sphingidae, with the highest endemism and richness in the Andes and Caribbean-Mesoamerica. We integrated phylogenomic and DNA barcode data and generated the first time-calibrated tree for this genus, covering 93.8% of the species diversity. We used event-based likelihood ancestral area estimation and biogeographic stochastic mapping to examine the speciation and dispersal dynamics of Xylophanes across bioregions. We also used trait-dependent diversification models to compare speciation and extinction rates of lineages associated with different bioregions. Our results indicate that Xylophanes originated in Caribbean-Mesoamerica in the Late Miocene, and immediately diverged into five major clades. The current species diversity and distribution of Xylophanes can be explained by two consecutive phases. In the first phase, the highest Xylophanes speciation and emigration rates occurred in the Caribbean-Mesoamerica, and the highest immigration rates occurred in the Andes, whereas in the second phase the highest immigration rates were found in Amazonia, and the Andes had the highest speciation and emigration rates.</p>
Data from: A diversification relay race from Caribbean-Mesoamerica to the Andes: historical biogeography of Xylophanes hawkmoths
Open the record for dataset details and reuse information.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
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
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.