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.
4,368
datasets available to search
ShareScore release 0.9.0
Dataset results
4,368 results for “male description”
Figure 3 in First records of Aganainae (Lepidoptera: Erebidae) from Zanzibar Island with a description of the male of Phaegorista bisignibasis Prout, 1918
Figure 3. Aganainae from Kiwengwa Forest, Zanzibar Island, Tanzania. (A-B) Asota speciosa (Drury, 1773). (C) Asota speciosa var. undulifera Walker 1856. (D) Soloe tripunctata Druce 1896. Scale bar = 10 mm. (Photos: Elizaveta A. Spitsyna).
Figures 28–33. Male genitalia. 28–31. P. otus. 28 in Notes on Pachypasa otus and the description of a new Iranian Pachypasa species (Lepidoptera, Lasiocampidae, Lasiocampinae, Lasiocampini)
Figures 28–33. Male genitalia. 28–31. P. otus. 28. Greece, Crete, genitalia slide 13.504 (MWM/ZSM). 29. SW Turkey, Alanya, genitalia slide otus-1 (CGM). 30. SE Turkey, Province Van, genitalia slide 8017 (MWM/ZSM). 31. Israel, N Golan Heights, genitalia slide 10.632 (MWM/ZSM). 32. Israel, Dead Sea, genitalia slide otus-3 (CGM). 33–34. P. hausmanni. 33. Holotype, Iran, Province Fars, genitalia slide hausm-1 (CGM). 34. Paratype, Iran, Province Kohgiluyeh and Boyer-Ahmad, genitalia slide hausm-2 (CGM). Scale bar – 1 mm.
Figs 16‒24 in First illustrated description of the male of Diphya macrophthalma, the type species of the genus (Araneae, Tetragnathidae)
Figs 16‒24. Male palp and epigyne of Diphya macrophthalma Nicolet, 1849: 16, 17 terminal part of palp with removed bulb, ventro-retrolateral, retrolateral and dorso-retrolateral; 19‒21 bUlb, dorsal, anterior and prolateral-anterior; 22 epigyne, ventral; 23 epigyne, dorsal; 24 anterior chamber of receptacle with glands (Am, accompanying membrane; Co, conductor; Cd, copulatory ducts; Da, dorso-retrolateral apophysis; Em, embolus; Ef, epigynal furrow; Ev, embolus ventrally; Fo, fovea; Gc, gland cilia; Mp, median plate; Oc, copulatory opening; Pc, central plate; Pd, dorsal part of paracymbium; Pi, pit; Pm, marginal plate. Scale = 0.1 mm if not otherwise indicated.
Figs 9‒15 in First illustrated description of the male of Diphya macrophthalma, the type species of the genus (Araneae, Tetragnathidae)
Figs 9‒15. Male palp of Diphya macrophthalma Nicolet, 1849: 9, whole palp, retrolateral; 10, 11, terminal part of palp, retro-ventral and antero-ventral; 12, same, prolateral; 13, 14 same, anterior and dorsal; 15, terminal part of the bulb, retrolateral (Am, accompanying membrane; Co, conductor; Da, dorso-retrolateral apophysis; Em, embolus; Ev, embolus ventrally; Pd, spine like dorsal part; Tg, tegulum). Scale = 0.2 mm.
Figs 1‒8 in First illustrated description of the male of Diphya macrophthalma, the type species of the genus (Araneae, Tetragnathidae)
Figs 1‒8. Somatic characters of Diphya macrophthalma Nicolet, 1849: 1, 2, female habitus, dorsal; 3, female habitus, ventral; 4, 5, male prosoma, frontal and dorsal; 6, male habitus, dorsal; 7, male prosoma, ventral; 8, female prosoma, ventral. Fig. 2, holotype, made by Tanikawa. Scale = 0.2 mm if not otherwise indicated.
Figs 25‒35. Diphya macrophthalma Nicolet, 1849 in First illustrated description of the male of Diphya macrophthalma, the type species of the genus (Araneae, Tetragnathidae)
Figs 25‒35. Diphya macrophthalma Nicolet, 1849 (Figs 25‒30, 33‒35) and D. rugosa Tullgren, 1902 (Figs 31, 32): 25, 26, 29‒32 epigyne, ventral; 27, 28 epigyne, dorsal; 33 paracymbium and tibia, ventro-retrolateral; 34, male epigastral area showing epiandrous spigots; 35, male spinnerets; 29, 30 holotype; 31, 32 syntype. Figs 30, 32 after TANIKAWA (1995). Figs 29, 31 made by A. Tanikawa (Ap, anterior pockets; Cd, copulatory ducts; Pc, central plate; Pl, mating plug; Pm, marginal plate; Ra, anterior chambers of receptacles; Rp, posterior chambers of receptacles).
Figs 1–8. Trypogeus Lacordaire, 1869, males. 1–3, 8 – T in The longicorn beetle genus Trypogeus Lacordaire, 1869 (Coleoptera: Cerambycidae) in Vietnam, with descriptions of three new species
Figs 1–8. Trypogeus Lacordaire, 1869, males. 1–3, 8 – T. pygmaeus sp. n., holotype; 4–5, 7 – T. superbus Pic, 1922; 6 – T. gressitti Miroshnikov, 2014, holotype. 1–2, 4 – habitus: 1, 4 – dorsal view, 2 – ventral view; 3, 5–6 – head, ventral view; 7 – head and pronotum; 8 – head, pronotum and base of elytra. Рис. 1–8. Trypogeus Lacordaire, 1869, самцы. 1–3, 8 – T. pygmaeus sp. n., гоΛотип; 4–5, 7 – T. superbus Pic, 1922; 6 – T. gressitti Miroshnikov, 2014, гоΛотип. 1–2, 4 – общий виÃ: 1, 4 – сверху, 2 – снизу; 3, 5–6 – гоΛова снизу; 7 – гоΛова и переÃнеспинка; 8 – гоΛова, переÃнеспинка и основание наÃкрыΛий.
Figure 10 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 10: Phylogenetic relationships within LONgidOrUS and ParalONgidOrUS. Bayesian 50% majority rule consensus tree as inferred from D2 and D3 expansion segments of 28S rRNA sequence alignment under the general time-reversible model of sequence evolution with correction for invariable sites and a gamma-shaped distribution (GTR + I + G: –lnL = 14601.9935; AIC = 29619.9870; freqA = 0.2204; freqC = 0.2274; freqG = 0.2934; freqT = 0.2588; R(a) = 0.7487; R(b) = 2.4740; R(c) = 1.4407; R(d) = 0.3992; R(e) = 4.6932; R(f) = 1.0000; Pinva = 0.2290; and Shape = 0.6290). Posterior probabilities greater than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changes per site.
Figure 9 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 9: Relationship of body length to length of functional and replacement odontostyle (= Odontostyle and • = replACement ODOntOStyle); length in three developmental stages and mature females of LONgidOrUS JONeSi.
Figure 8 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 8: Scanning electron microscopy of LONgidOrUS JONeSi (Siddiqi, 1962). A–D, Female head region in lateral and ventrolateral view showing internal (ip) and outer labial papillae (op), oral aperture (oa), stylet (st), and amphidial aperture (aa); E–F, Female tail in lateral view (a = anus); G–H, Vulval region in lateral and ventral view (v = vulva). (Scale bars: A–D = 5 μm; E = 10 μm; F = 20 μm; G–H = 30 μm).
Figure 6 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 6: Light micrographs of LONgidOrUS JONeSi (Siddiqi, 1962). Male and first-stage juvenile. A, Entire body of male; B, Anterior region of male; C, Tail region of male arrows showing position of supplements (spl); D, Entire body of J1; E, ANterior region of J1 arrows showing position of guiding ring (gr) and replacement odontostyle (rodt); F–G, Tail regions of J1. (Scale bars: A = 200 μm; B–C = 40 μm; D = 100 μm; E–G = 10 μm).
Figure 3 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 3: Scanning electron microscopy of ParalONgidOrUS Sali (Siddiqi et al., 1963). A–C, Female head region in lateral and ventrolateral view showing internal (ip) and outer labial papillae (op), cephalic lobe (cl), cephalic papillae (cp), oral aperture (oa), and amphidial aperture (aa). D–E, Female tail in lateral and ventral view (a = anus). F–G: Vulval region (v = vulva). (Scale bars: A–C = 5 μm; D = 30 μm; E, F = 10 μm; G = 20 μm).
Figure 2 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 2: Light micrographs of ParalONgidOrUS Sali (Siddiqi et al., 1963). A–D, lip region of 1st, 2nd, and 3rd stage juveniles and female; E–H, Tail region of 1st, 2nd, and 3rd stage juveniles and female (Scale bars: A–H = 10 μm).
Figure 1 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 1: Light micrographs of ParalONgidOrUS Sali (Siddiqi et al., 1963). Female: A, Pharynx; B–D, Lip region arrow showing amphid; E, Gonad; F, Tail region arrow showing position of anus G, Tail region arrows showing position of caudal pores; H, Ventral view of vulva; I, Vulval region (Scale bars: A = 50 μm; B–D= 10 μm; E= 50 μm; F–I= 10 μm).
Figure 11 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 11: Phylogenetic relationships within LONgidOrUS and ParalONgidOrUS. Bayesian 50% majority rule consensus tree as inferred from 18S rRNA gene sequence alignment under a transitional of invariable sites model with invariable sites and a gamma-shaped distribution (TIM2 + I + G: – lnL= 6866.9821; AIC = 14129.9643; freqA = 0.2626; freqC = 0.2109; freqG = 0.2668; freqT = 0.2597; R(a) = 1.8892; R(b) = 3.9662; R(c) = 1.8892; R(d) = 1.0000; R(e) = 7.1009; R(f) = 1.0000; Pinva = 0.7060; and Shape = 0.6020). Posterior probabilities greater than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changes per site.
Figure 7 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 7: Light micrographs of LONgidOrUS JONeSi (Siddiqi, 1962). A–D, lip region of 1st, 2nd, 3rd, and 4th stage juveniles; E–H, Tail region of 1st, 2nd, 3rd, and 4th stage juveniles (Scale bars: A–H = 10 μm).
Figure 5 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 5: Light micrographs of LONgidOrUS JONeSi (Siddiqi, 1962). Female: A, Pharynx; B–E, Lip regions; F, Gonad; G–H, Pharyngeal bulb; I, Entire female body; J–K, Vulval regions; L, ventral view of tail; M–O, Female tails (Scale bars: A = 50 μm; B–E, G–H, J–O = 10 μm; F = 20 μm; I = 500 μm) am = amphid; bp = body pores; v = vulva; svn = subventrolateral nuclei; dn = dorsal nuclei; a = anus).
Figure 4 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 4: Relationship of body length to length of functional and replacement odontostyle (= Odontostyle and • = replACement ODOntOStyle); length in three developmental stages and mature females of ParalONgidOrUS Sali.
Fig. 7 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes
Fig. 7. Maximum likelihood (ML) phylogenetic tree from entire mt genomes (15,254 bp alignment). Tip-labels indicate NCBI accession numbers. Numbers above branches show Maximum Likelihood bootstrap support whereas numbers below branches show the Bayesian Posterior Probability support. Ixodes pavlovskyi Pomerantzev, 1946, one of the species of "other Ixodes" clade (sensu Barker et al., 2021), for which an entire mitochondrial (mt) genome was available in GenBank, was set as the outgroup. The scale bar indicates 0.07 nucleotide substitutions per nucleotide site for the 15,254 nucleotide sites in our alignment of theses entire mt genomes. So, for example, there were about 1067 nucleotide substitutions along the branch that leads to I. (Ceratixodes) uriae plus I. (Sternalixodes) holocyclus plus I. (Exopalpiger) fecialis, which is marked with an asterisk (i.e. 0.07 nucleotide substitutions per nucleotide site x 15,254 nucleotide sites (bps) = 1067 nucleotide substitutions). Ticks in bold were sequenced in the present study.
Fig. 6 in Rediscovery of Ixodes confusus in Australia with the first description of the male from Australia, a redescription of the female and the mitochondrial (mt) genomes of five species of Ixodes
Fig. 6. The mitochondrial genomes of Ixodes (Sternalixodes) confusus, I. (St.) myrmecobii, I. (St.) cornuatus, I. (St.) hirsti and I. (St.) trichosuri. Protein-coding genes are shown in green, tRNAs are in yellow, rRNAs are in red whereas the two control regions are in blue. Protein-coding genes are labelled by their fourcharacter abbreviations, tRNAs are labelled by their one-letter amino acid abbreviations whereas the two control regions are labelled as CR1 and CR2. Variation in the size of mitochondrial genome is indicated in parenthesis. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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.