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250 results for “Cyphophthalmi”
Figure 14 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 14. Cyphophthalmus gordani sp. nov. (holotype except B, F – female paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 35. A in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 35. A, geographical distribution of the three phylogenetic lines of the genus Cyphophthalmus (signs often cover more than one locality); B, distribution of presented species in south-eastern part of the Balkan Peninsula.
Figure 34 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 34. Cyphophthalmus hlavaci sp. nov. (paratypes from Bast). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 6 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 6. Detail of integument ornamentation of the third opisthosomal segment, dorsal. A, Cyphophthalmus corfuanus (Kratochvíl); B, Cyphophthalmus zetae sp. nov.; C, Cyphophthalmus martensi sp. nov.; D, Cyphophthalmus beschkovi (Mitov); E, Cyphophthalmus sp. (Cave, Mt. Biokovo, Dalmatia); F, Cyphophthalmus noctiphilus (Kratochvíl).
Figure 5 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 5. Distal portion of ovipositor (left terminal lobe excluded), ventral view. A, Cyphophthalmus minutus (Kratochvíl) topotype; B, Cyphophthalmus gordani sp. nov.; C, Cyphophthalmus neretvanus sp. nov.; D, Cyphophthalmus trebinjanus sp. nov.; E, Cyphophthalmus ognjenovici sp. nov.; F, Cyphophthalmus rumijae sp. nov.; G, Cyphophthalmus martensi sp. nov. Circles represent insertion of ventral setae; x represent insertion of dorsal setae. Scale bar = 100 Mm.
Figure 4 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 4. Distal portion of ovipositor (left terminal lobe excluded), ventral view. A, Cyphophthalmus gjorgjevici (Hadži), (Rašće, Macedonia); B, Cyphophthalmus paragamiani sp. nov.; C, Cyphophthalmus thracicus sp. nov.; D, Cyphophthalmus cf. thracicus (Evros, Greece); E, Cyphophthalmus corfuanus (Kratochvíl) (Corfu); F, Cyphophthalmus zetae sp. nov.; G, Cyphophthalmus hlavaci sp. nov. Circles represent insertion of ventral setae; x represent insertion of dorsal setae. Scale bar = 100 Mm.
Figure 7 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 7. Cyphophthalmus paragamiani sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 3. Male anal regions. A–B in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 3. Male anal regions. A–B, Cyphophthalmus corfuanus (Kratochvíl); C, Cyphophthalmus serbicus (Hadži); D, Cyphophthalmus ere Karaman; E, Cyphophthalmus ognjenovici sp. nov.; F, Cyphophthalmus duricorius Joseph.
Figure 1. A, C in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 1. A, C, Siro exilis Hoffman, 1963 (West Virginia, Summers County). A, spermatopositor, dorsal view; C, ventral prosomal complex. B, D, Cyphophthalmus teyrovskyi (Kratochvíl, 1938). B, spermatopositor, dorsal view; D, ventral prosomal complex. Not to scale.
Figure 2. A–B, spiracles. A in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 2. A–B, spiracles. A, Siro exilis Hoffman (West Virginia, Summers County), light micoscopy microphotograph; B, Cyphophthalmus hlavaci sp. nov., scanning electron micrograph. C–D, outlet ducts and pores of anal glands. C, S. exilis Hoffman (West Virginia, Summers County); D, Cyphophthalmus serbicus (Hadži). E–F, spermatopositor movable fingers (digiti mobiles). E, Cyphophthalmus cf. zetae sp. nov. (Manastir Morača, Montenegro); F, Cyphophthalmus gordani sp. nov. Not to scale.
Figure 8 in The Iberian Peninsula: ancient history of a hot spot of mite harvestmen (Arachnida: Opiliones: Cyphophthalmi: Sironidae) diversity
Figure 8. Paramiopsalis eduardoi sp. nov., confocal laser scanning micrograph of the spermatopositor of a male paratype, dorsal view. Total length is 180 Mm.
Figure 5 in The Iberian Peninsula: ancient history of a hot spot of mite harvestmen (Arachnida: Opiliones: Cyphophthalmi: Sironidae) diversity
Figure 5. Paramiopsalis eduardoi sp. nov., scanning electron microgarphs of a male paratype. A, ventral view of whole body. B, ozophore. C, prosomal ventral complex. D, anal region. E, spiracle.
Figure 4 in The Iberian Peninsula: ancient history of a hot spot of mite harvestmen (Arachnida: Opiliones: Cyphophthalmi: Sironidae) diversity
Figure 4. Paramiopsalis eduardoi sp. nov., paratype female. A, dorsal view. B, ventral view. C, lateral view. Scale bars: 0.5 mm.
Figure 9 in The Iberian Peninsula: ancient history of a hot spot of mite harvestmen (Arachnida: Opiliones: Cyphophthalmi: Sironidae) diversity
Figure 9. Phylogeny of selected members of the family Sironidae, based on the combined analysis of 18S, 28S, cytochrome c oxidase subunit I (COI), and 16S under direct optimization and equal weighting. The support values on branches indicate the jackknife frequencies. Each weighting scheme is assigned a code corresponding to the ratio of indel/transversion, transversion/transition, and transition values. Tree lengths for the different parameter sets are as follows: 111, 2914; 121, 4585; 211, 3228; 3221, 6168. Black squares indicate monophyly; grey squares indicate that either the group is paraphyletic or the internal relationships are different.
Figure 7 in The Iberian Peninsula: ancient history of a hot spot of mite harvestmen (Arachnida: Opiliones: Cyphophthalmi: Sironidae) diversity
Figure 7. Paramiopsalis eduardoi sp. nov., scanning electron microgarphs of the legs of a male paratype. A, metatarsus and tarsus I. B, tarsal claw I. C, metatarsus and tarsus II. D, tarsal claw II. E, metatarsus and tarsus III. F, tarsal claw III. G, metatarsus and tarsus IV. H, detail of the adenostyle. I, tarsal claw IV.
Figure 2. Parasiro coiffaiti Juberthie, 1956, lectotype male. A, dorsal view. B, ventral view. C in The Iberian Peninsula: ancient history of a hot spot of mite harvestmen (Arachnida: Opiliones: Cyphophthalmi: Sironidae) diversity
Figure 2. Parasiro coiffaiti Juberthie, 1956, lectotype male. A, dorsal view. B, ventral view. C, lateral view. Scale bars: 0.5 mm.
FIGURES 1 – 2 in A new Afrotropical Ogovea (Opiliones, Cyphophthalmi) from Cameroon, with a discussion on the taxonomic characters in the family Ogoveidae
FIGURES 1 – 2. Holotype of Ogovea cameroonensis sp. n. 1. Dorsal view; 2. Ventral view.
FIGURE 5 in A new Miopsalis from Mindanao supports a biogeographic umbilicus between Borneo and the southern Philippines (Arachnida: Opiliones: Cyphophthalmi: Stylocellidae)
FIGURE 5. Left: Schematic of complete phylogeny inferred from maximum likelihood analysis of four molecular loci (lnL = -41177.18), showing major groups of Opiliones. Right: Detail of phylogenetic relationships and geographical origins of Miopsalis specimens. Numbers on nodes indicate ultrafast bootstrap resampling frequencies.
FIGURE 4 in A new Miopsalis from Mindanao supports a biogeographic umbilicus between Borneo and the southern Philippines (Arachnida: Opiliones: Cyphophthalmi: Stylocellidae)
FIGURE 4. Miopsalis dilly sp. nov. (A) Spermatopositor, dorsal view. (B) Same, ventral view. (C) Detail of the gonopore complex. Scale bars as indicated.
FIGURE 2 in A new Miopsalis from Mindanao supports a biogeographic umbilicus between Borneo and the southern Philippines (Arachnida: Opiliones: Cyphophthalmi: Stylocellidae)
FIGURE 2. Miopsalis dilly sp. nov. (A) Male paratype, ventral view of prosomal complex. (B) Female paratype, same. (C) Male paratype, ventral view of posterior part of opisthosoma. (D) Female paratype, same. Scale bars: 500 µm.
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