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.
312
datasets available to search
ShareScore release 0.7.1
Dataset results
312 results for “Diplura”
Figure 6 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography
Figure 6. Olfactory chemoreceptor of the last antennomere in soil-adapted species: A, Campodea (Paurocampa) suensoni Tuxen, 1930 from Dos Aguas, Valencia, Spain; and cave-adapted species: B, Cycladiacampa irakleiae Sendra, 2020 from Spilaio Ioanni Cave, Irakleia Island, Greece; C, Pacificampa daidarabotchi Sendra, 2018 from Mejito-do Cave, Kyushu Island, Japan; D, undescribed Plusiocampinae from Huitième Ciel Cave. Banqiao, Hubei, China; E, Turkmenocampa mirabilis Sendra & Stoev, 2017 from Kaptarhana Cave, Koytendog District, Lebap, Turkmenistan; F, Remycampa herbanica from Montaña Blanca Cave, Fuerteventura Island, Spain.
Figure 5 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography
Figure 5. Bar chart showing the relative number of soil (orange) and cave-adapted (blue) dipluran species per family, subfamily and genus.
Figure 16 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 16. Scanning electron micrographs of the secretion. A, distal end of the infudibuliform complex with the extruded filaments. B, C, detail of filaments showing the granular surface.
Figure 15 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 15. Scanning electron micrographs of the cerci of Recent projapygids (genera indet.) expelling the glandular substance. A–C, different magnifications of cerci of a specimen from Brazil showing the solidified secretion forming filamentous masses. D, distal part of cerci of a Costa Rican specimen showing an incipient secretion. Arrows indicate the glandular substance in C and D. In A, the box labelled B corresponds to panel B; In B, the box labelled C corresponds to panel C. Abbreviations: ids, infundibuliform distal segment; ipds, infundibuliform predistal segment; ss, simple setae; tp, longitudinal tegumentary pleats. Scale bars: 1 mm in A; 0.2 mm in B; 0.05 mm in C, D.
Figure 14 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 14. Palaeoecological reconstruction of Electroprojapyx alchemicus gen. et sp. nov, using their cerci as chemical weapons for hunting a springtail in the Cretaceous amber forest. Illustration by O. Sanisidro, with scientific supervision.
Figure 8 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 8. Volume renderings of Symphylurinus sp. 1 (AMNH JZC-DR005) in Miocene Dominican amber. A, dorsal habitus. B, ventral habitus. C, right lateral habitus. All to the same scale. Scale bar: 1 mm.
Figure 7 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 7. Camera lucida drawings of Symphylurinus sp. 1 (AMNH JZC-DR005) in Miocene Dominican amber. A, left ventrolateral habitus. B, detail of right tarsi of leg III. C, right abdominal stylus V. D, right abdominal stylus VI. E, right abdominal stylus VII. F, detail of infundibuliform complex of left cercus. Abbreviations: a, apical macroseta; lp, labial palpus; M, sternal macroseta; sa, subapical macroseta; scA, lateral subcoxal appendage; stI–stVII, stylus I–VII; vm, ventromedial macroseta. C–F are to the same scale. Scale bars: 0.5 mm in A; 0.2 mm in B; 0.1 mm in C–F.
Figure 5 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 5. Volume renderings of holotype of Symphylurinopsis punctatus gen. et sp. nov. (M-2232) in Miocene Dominican amber. A, dorsal habitus. B, ventral habitus. C, left lateral habitus. All to the same scale. Scale bar: 1 mm.
Figure 1 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 1. Scanning electron micrographs of Recent specimens representing the two body plans of predatory diplurans. A, Japygoidea specimen from Malta, dorsal view. B, Projapygoidea specimen from Thailand, ventral view. C, detail of cercal forceps. D, detail of right cercus. Scale bars: 2 mm in A; 0.5 mm in B.
Figure 4 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 4. Camera lucida drawings of holotype of Symphylurinopsis punctatus gen. et sp. nov. (M-2232) in Miocene Dominican amber. A, detail of cerci. B, dorsal habitus. Abbreviations: lp, labial palp; scA, lateral subcoxal appendage; stI– stVII, stylus I–VII. Scale bars: 0.5 mm.
Figure 3 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 3. Photomicrographs of holotype of Symphylurinopsis punctatus gen. et sp. nov. (M-2232) in Miocene Dominican amber. A, dorsal habitus. B, detail of setigerous punctures on tergites IV–VII. C, detail of head. D, detail of cerci in ventral view. Abbreviations: gp, genital papilla; lp, labial palp; mp, maxillary palp; stVII, stylus VII. Scale bars: 0.5 mm in A; 0.1 mm in B–D.
Figure 2 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 2. Holotype of Electroprojapyx alchemicus gen. et sp. nov. (AMNH JZCBu-1957) in Cretaceous Burmese amber. A, photomicrographs of left ventrolateral habitus of the dipluran fossilized in a preying-and-spraying position with its prey. B, detail of cerci with arrows pointing to the secreted substance. C, camera lucida drawing of the specimen with the secreted filaments in red. D, detail of antennae of the dipluran with the Collembola between them. Abbreviations: b, bubble; scA, lateral subcoxal appendage; stII–stVII, stylus II–VII. Scale bars: 0.5 mm in A, C, D; 0.1 mm in B.
Fig. 6 in New evidence for an Anatolian bridge: Colonization of Euromediterranean lands by cave-adapted Plusiocampinae (Diplura, Campodeidae), with establishment of a new genus
Fig. 6. SEM micrographs of Anatoliacampa diclensis Sendra, Tusun & Satar gen. et sp. nov. (a) Right eversible vesicle on an abdominal segment. (b) Right stylus on abdominal segment IV. Abbreviations: a, apical; sa, subapical; and m, medial macrosetae.
Fig. 1 in New evidence for an Anatolian bridge: Colonization of Euromediterranean lands by cave-adapted Plusiocampinae (Diplura, Campodeidae), with establishment of a new genus
Fig. 1. SEM micrographs of Anatoliacampa diclensis Sendra, Tusun & Satar gen. et sp. nov. (a) Cupuliform organ of the apical antennomere. (b) Detail of sensilla of the cupuliform organ. (c) Lateral view of the apical antennomere. (d) Glandular setae on the exterior rim of the cupuliform organ. (e) Detail of apical portion of glandular setae. (f) Detail of medial portion of gouge sensilla.
Fig. 2 in New evidence for an Anatolian bridge: Colonization of Euromediterranean lands by cave-adapted Plusiocampinae (Diplura, Campodeidae), with establishment of a new genus
Fig. 2. SEM micrographs of Anatoliacampa diclensis Sendra, Tusun & Satar gen. et sp. nov. (a) Medial antennomeres. (b) Proximal antennomeres. (c) Distal gouge sensilla on a medial antennomere. (d) Detail of central portion of gouge sensilla. Abbreviation: ft, flagellum of the trichobothria.
Fig. 5 in New evidence for an Anatolian bridge: Colonization of Euromediterranean lands by cave-adapted Plusiocampinae (Diplura, Campodeidae), with establishment of a new genus
Fig. 5. Anatoliacampa diclensis Sendra, Tusun & Satar gen. et sp. nov. (a) Urosternite I of the male, 6- paratype (MZB (MCNB) 2022-5694). (b) Urosternite I of the female, ♀- holotype (DUZM-2121). Abbreviation: a1, glandular a1 setae.
Fig. 9 in New evidence for an Anatolian bridge: Colonization of Euromediterranean lands by cave-adapted Plusiocampinae (Diplura, Campodeidae), with establishment of a new genus
Fig. 9. Maximum likelihood (ML) tree obtained from CO1 sequence data showing significant (>70) bootstrap support values. Anatoliacampa clustered with Plusiocampinae representatives from Turkey and Bulgaria.
Fig. 8 in New evidence for an Anatolian bridge: Colonization of Euromediterranean lands by cave-adapted Plusiocampinae (Diplura, Campodeidae), with establishment of a new genus
Fig. 8. Colonization way of Euromediterranean lands during the end of the Oligocene, 25 m. a. Abbreviations, taxonomic groups: Ces: Cestocampa; Par: Paratachycampa; Pat: Patrizicampa; Sty: Stygiocampa; Cycl: Cycladiacampa irakleiae; Anat: Anatoliacampa diclensis; Red highlights the current distribution of Plusiocampinae in Euromediterranean lands; the red arrow indicates the direction of the Plusiocampinae arrival from East Asia. source map © 2020 Colorado Plateau Geosystems Inc. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in New evidence for an Anatolian bridge: Colonization of Euromediterranean lands by cave-adapted Plusiocampinae (Diplura, Campodeidae), with establishment of a new genus
Fig. 4. SEM micrographs of Anatoliacampa diclensis Sendra, Tusun & Satar gen. et sp. nov., metathoracic leg. (a) Distal portion of the metathoracic leg. (b) Lateral view of pretarsus in upward position. (c) Detail of lateral crest of the pretarsus. (d) Dorsal proximal portion of lateral crest. (e) Lateral view of pretarsus in downward position. (f) Distal portion of the lateral processes of the pretarsus. Abbreviations: dm, dorsal macrosetae; vt, ventral macrosetae.
Fig. 3 in New evidence for an Anatolian bridge: Colonization of Euromediterranean lands by cave-adapted Plusiocampinae (Diplura, Campodeidae), with establishment of a new genus
Fig. 3. Thoracic nota of Anatoliacampa diclensis Sendra, Tusun & Satar gen. et sp. nov., ♀- holotype (DUZM-2121).
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.