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Рис. 3. Halalaimus borealis sp. nov., гоΛотип самца (А, В, Е) и паратип самки (Б, Г). А — переΑний конец теΛа; Б — теΛо в обΛасти вуΛьвы; В, Г — заΑний конец теΛа; Е — спикуΛы и руΛек. Масштаб: А, Б — 20 мкм; В, Г, Á — 30 мкм Fig. 3. Halalaimus borealis sp. nov., male holotype (А, В, Е) and female paratype (Б, Г). А — anterior body end; Б — vulva region; В, Г — posterior body end; Е — spicules and gubernaculum. Scale bars: А, Б — 20 μm; В, Г Á — 30 μm in Sp. Nov. And Sp. Nov. (Nematoda, Enoplida) From The Mouth Of The Cam River In Vietnam
Рис. 3. Halalaimus borealis sp. nov., гоΛотип самца (А, В, Е) и паратип самки (Б, Г). А — переΑний конец теΛа; Б — теΛо в обΛасти вуΛьвы; В, Г — заΑний конец теΛа; Е — спикуΛы и руΛек. Масштаб: А, Б — 20 мкм; В, Г, Á — 30 мкм Fig. 3. Halalaimus borealis sp. nov., male holotype (А, В, Е) and female paratype (Б, Г). А — anterior body end; Б — vulva region; В, Г — posterior body end; Е — spicules and gubernaculum. Scale bars: А, Б — 20 μm; В, Г Á — 30 μm
Рис. 1. Semophylax Meyrick: 1–4 — S. margaritae sp. nov. (1, 2 — бабочка; 3, 4 — генитаΛии самца: 3 — виà сбоку, 4 — ункус и гнатос); 5, 6 — S. decipens sp. nov. (5 — бабочка, 6 — генитаΛии самки) Fig. 1–6. Semophylax Meyrick: 1–4 — S. margaritae sp. nov. (1, 2 — adult; 3, 4 — male genitalia: 3 — lateral view, 4 — uncus and gnathos); 5, 6 — S. decipens sp. nov. (5 — adult, 6 — female genitalia) in Two New Species Of Gelechiid Moths Genus Semophylax Meyrick, 1932 (Lepidoptera, Gelechiidae) Found In Malaysia
Рис. 1. Semophylax Meyrick: 1–4 — S. margaritae sp. nov. (1, 2 — бабочка; 3, 4 — генитаΛии самца: 3 — виà сбоку, 4 — ункус и гнатос); 5, 6 — S. decipens sp. nov. (5 — бабочка, 6 — генитаΛии самки) Fig. 1–6. Semophylax Meyrick: 1–4 — S. margaritae sp. nov. (1, 2 — adult; 3, 4 — male genitalia: 3 — lateral view, 4 — uncus and gnathos); 5, 6 — S. decipens sp. nov. (5 — adult, 6 — female genitalia)
Рис. 2. Mukhina elegans (Mukhina, 1981) (самка): А — трофико-сенсорный отΔеΛ теΛа; Б — поΛовая система; В — переΔний конец теΛа; Г — хвост; À — фрагмент кутикуΛы с боковым поΛем бп — боковое поΛе, да — ΔробиΛьный аппарат, в — вуΛьва, зм — заΔняя матка, кб — карΔиаΛьный буΛьбус, кск — кΛетки среΔней кишки, нк — нервное коΛьцо, пм — переΔняя матка, р — ректум, рт — ренетта, с — сперма, ск — среΔняя кишка, сп — семяприемник, ф — фазмиΔы, хс — хейΛостома, эп — экскреторная пора, я — яичник Fig. 2. Mukhina elegans (Mukhina, 1981) (female): A — trophic-sensory part of the body; B — the reproductive system; C — the front end of the body; G — the tail; D — fragment of the cuticle with a side field бп — side field, да — crushing apparatus, в — vulva, зм — posterior uterus, кб — cardial bulb, кск — cells of the mid-intestine, нк — nerve ring, пм — anterior uterus, р — rectum, рт — renetta с — sperm, ск — mid-intestin, сп — seminal receptacle, ф — phasmids, хс — cheilostoma, эп — excretory pore, я — ovary in A New Species Sp. Nov. (Nematoda, Cephalobidae) From Primorsky Region (Russia)
Рис. 2. Mukhina elegans (Mukhina, 1981) (самка): А — трофико-сенсорный отΔеΛ теΛа; Б — поΛовая система; В — переΔний конец теΛа; Г — хвост; À — фрагмент кутикуΛы с боковым поΛем бп — боковое поΛе, да — ΔробиΛьный аппарат, в — вуΛьва, зм — заΔняя матка, кб — карΔиаΛьный буΛьбус, кск — кΛетки среΔней кишки, нк — нервное коΛьцо, пм — переΔняя матка, р — ректум, рт — ренетта, с — сперма, ск — среΔняя кишка, сп — семяприемник, ф — фазмиΔы, хс — хейΛостома, эп — экскреторная пора, я — яичник Fig. 2. Mukhina elegans (Mukhina, 1981) (female): A — trophic-sensory part of the body; B — the reproductive system; C — the front end of the body; G — the tail; D — fragment of the cuticle with a side field бп — side field, да — crushing apparatus, в — vulva, зм — posterior uterus, кб — cardial bulb, кск — cells of the mid-intestine, нк — nerve ring, пм — anterior uterus, р — rectum, рт — renetta с — sperm, ск — mid-intestin, сп — seminal receptacle, ф — phasmids, хс — cheilostoma, эп — excretory pore, я — ovary
Рис. 1. Mukhina orientalis sp. nov. (самка): А — трофико-сенсорный отΔеΛ теΛа; Б — генитаΛьнокауΔаΛьный отΔеΛ теΛа; В — трофико-сенсорный отΔеΛ теΛа второй самки; Г — переΔний конец теΛа; À — хвост второй самки бп — боковое поΛе, да — ΔробиΛьный аппарат, в — вуΛьва, зм — заΔняя матка, кб — карΔиаΛьный буΛьбус, нк — нервное коΛьцо, пм — переΔняя матка, р — ректум, рт — ренетта, ск — среΔняя кишка, скλ — скΛероции кутикуΛы, сп — семяприемник, ф — фазмиΔы, хс — хейΛостома, эп — экскреторная пора, я — яичник Fig. 1. Mukhina orientalis sp. nov. (female): A — trophic-sensory part of the body; Б — genitalcaudal part of the body; В — trophic-sensory part of the body of the second female; Г — front end of the body; À — tail of the second female бп — side field, да — crushing apparatus, в — vulva, зм — posterior uterus, кб — cardial bulb, нк — nerve ring, пм — anterior uterus, р — rectum, ск — mid-intestine, скλ — sclerotic cuticle, сп — seminal receptacle, ф — phasmids, хс — cheilostoma, эп — excretory pore, я — ovary in A New Species Sp. Nov. (Nematoda, Cephalobidae) From Primorsky Region (Russia)
Рис. 1. Mukhina orientalis sp. nov. (самка): А — трофико-сенсорный отΔеΛ теΛа; Б — генитаΛьнокауΔаΛьный отΔеΛ теΛа; В — трофико-сенсорный отΔеΛ теΛа второй самки; Г — переΔний конец теΛа; À — хвост второй самки бп — боковое поΛе, да — ΔробиΛьный аппарат, в — вуΛьва, зм — заΔняя матка, кб — карΔиаΛьный буΛьбус, нк — нервное коΛьцо, пм — переΔняя матка, р — ректум, рт — ренетта, ск — среΔняя кишка, скλ — скΛероции кутикуΛы, сп — семяприемник, ф — фазмиΔы, хс — хейΛостома, эп — экскреторная пора, я — яичник Fig. 1. Mukhina orientalis sp. nov. (female): A — trophic-sensory part of the body; Б — genitalcaudal part of the body; В — trophic-sensory part of the body of the second female; Г — front end of the body; À — tail of the second female бп — side field, да — crushing apparatus, в — vulva, зм — posterior uterus, кб — cardial bulb, нк — nerve ring, пм — anterior uterus, р — rectum, ск — mid-intestine, скλ — sclerotic cuticle, сп — seminal receptacle, ф — phasmids, хс — cheilostoma, эп — excretory pore, я — ovary
→ Fig. 2. Representative skeletal elements of ornithosuchid archosaur Dynamosuchus collisensis gen. et sp. nov. (CAPPA/UFSM 0248) from Janner outcrop, Carnian, Late Triassic. A. Selected skull bones in left lateral view. B. Reconstruction of the skull. C. Skull in ventral view. D. Left quadrate and quadratojugal in posterodorsal view. E. Parabasisphenoid in left lateral view. F. Neural arch of an anterior cervical vertebra in anterior view. G. Centrum of a cervical vertebra in left lateral view. H. Right osteoderm in dorsal view. I. Neural arch of an anterior dorsal vertebra in left lateral view. J. Left ilium in lateral view. L. Right humerus in anterior view. M. Right forearm in medial view. N. Left manus in dorsal view. O. Right (reversed) pubis in lateral view. P. Left femur in anterior view. Q. Left fibula in lateral view. Some unpreserved portions are modified from Baczko et al. in press, for the reconstruction of the skeleton of CAPPA/UFSM 0248 (preserved elements indicated in orange) (K). Scale bars 20 mm. in The first ornithosuchid from Brazil and its macroevolutionary and phylogenetic implications for Late Triassic faunas in Gondwana
→ Fig. 2. Representative skeletal elements of ornithosuchid archosaur Dynamosuchus collisensis gen. et sp. nov. (CAPPA/UFSM 0248) from Janner outcrop, Carnian, Late Triassic. A. Selected skull bones in left lateral view. B. Reconstruction of the skull. C. Skull in ventral view. D. Left quadrate and quadratojugal in posterodorsal view. E. Parabasisphenoid in left lateral view. F. Neural arch of an anterior cervical vertebra in anterior view. G. Centrum of a cervical vertebra in left lateral view. H. Right osteoderm in dorsal view. I. Neural arch of an anterior dorsal vertebra in left lateral view. J. Left ilium in lateral view. L. Right humerus in anterior view. M. Right forearm in medial view. N. Left manus in dorsal view. O. Right (reversed) pubis in lateral view. P. Left femur in anterior view. Q. Left fibula in lateral view. Some unpreserved portions are modified from Baczko et al. in press, for the reconstruction of the skeleton of CAPPA/UFSM 0248 (preserved elements indicated in orange) (K). Scale bars 20 mm.
Paratype male of Cynolebias alexandri sp. nov. from Gualeguaychu, Provincia de Entre Rios, Argentina. Photo by Dr. Hugo P. Castello. in Cynolebias alexandri, a new species of annual killifish from Argentina, with notes on C. bellottii
Paratype male of Cynolebias alexandri sp. nov. from Gualeguaychu, Provincia de Entre Rios, Argentina. Photo by Dr. Hugo P. Castello.
Рис. 3. Bolbolaimus brevis sp. nov., самец (А, Б, Δ) и самка (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 7 мкм; Б, Г, Δ — 20 мкм; В — 30 мкм Fig. 3. Bolbolaimus brevis sp. nov., male (А, Б, Δ) and female (В, Г). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 7 µm; Б, Г, Δ – 20 µm; В – 30 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 3. Bolbolaimus brevis sp. nov., самец (А, Б, Δ) и самка (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 7 мкм; Б, Г, Δ — 20 мкм; В — 30 мкм Fig. 3. Bolbolaimus brevis sp. nov., male (А, Б, Δ) and female (В, Г). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 7 µm; Б, Г, Δ – 20 µm; В – 30 µm
Рис. 2. Фотографии Bolbolaimus parvus sp. nov., самец (А, В, Δ, Е, Ж, К, Α) и самка (Б, Г, З, И, М). А, Б — общий виΑ; В, Г — переΑний конец теΛа; Δ — теΛо в обΛасти базаΛьного буΛьбуса; Е, Ж, З — гоΛова; И — теΛо в обΛасти вуΛьвы; К — теΛо в обΛасти кΛоаки; Α, М — хвост. Масштаб: Б — 100 мкм; А — 50 мкм; В, Α — 20 мкм; Г, И, М — 10 мкм; Δ, Е, Ж, З, К — 5 мкм Fig. 2. Light micrograph of Bolbolaimus parvus sp. nov., male (А, В, Δ, Е, Ж, К, Α) and female (Б, Г, З, И, М). А, Б – general view; В, Г – anterior body end; body in region of basal pharynx bulb; Е, Ж, З – head; И – vulva region; К – cloaca region; Α, М – tail. Scale bars: Б – 100 µm; А – 50 µm; В, Α – 20 µm; Г, И, М – 10 µm; Δ, Е, Ж, З, К – 5 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 2. Фотографии Bolbolaimus parvus sp. nov., самец (А, В, Δ, Е, Ж, К, Α) и самка (Б, Г, З, И, М). А, Б — общий виΑ; В, Г — переΑний конец теΛа; Δ — теΛо в обΛасти базаΛьного буΛьбуса; Е, Ж, З — гоΛова; И — теΛо в обΛасти вуΛьвы; К — теΛо в обΛасти кΛоаки; Α, М — хвост. Масштаб: Б — 100 мкм; А — 50 мкм; В, Α — 20 мкм; Г, И, М — 10 мкм; Δ, Е, Ж, З, К — 5 мкм Fig. 2. Light micrograph of Bolbolaimus parvus sp. nov., male (А, В, Δ, Е, Ж, К, Α) and female (Б, Г, З, И, М). А, Б – general view; В, Г – anterior body end; body in region of basal pharynx bulb; Е, Ж, З – head; И – vulva region; К – cloaca region; Α, М – tail. Scale bars: Б – 100 µm; А – 50 µm; В, Α – 20 µm; Г, И, М – 10 µm; Δ, Е, Ж, З, К – 5 µm
Рис. 1. Bolbolaimus parvus sp. nov., самец (А, Б, В) и самка (Г, Δ). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 10 мкм; В, Δ — 20 мкм; Б, Г — 30 мкм Fig. 1. Bolbolaimus parvus sp. nov., male (А, Б, В) and female (Г, Δ). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 10 µm; В, Δ – 20 µm; Б, Г – 30 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 1. Bolbolaimus parvus sp. nov., самец (А, Б, В) и самка (Г, Δ). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 10 мкм; В, Δ — 20 мкм; Б, Г — 30 мкм Fig. 1. Bolbolaimus parvus sp. nov., male (А, Б, В) and female (Г, Δ). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 10 µm; В, Δ – 20 µm; Б, Г – 30 µm
Рис. 4. Фотографии Bolbolaimus brevis sp. nov., самец (А, В, Г, Е, З, И, К) и самка (Б, Δ, Ж, Α). А, Б — общий виΑ; В, Г, Δ — гоΛова; Е — переΑний конец теΛа; Ж — теΛо в обΛасти вуΛьвы; З, И — теΛо в обΛасти кΛоаки; К, Α — хвост. Масштаб: А, Б — 50 мкм; Е, Ж, К, Α — 10 мкм; В, Г, Δ, З, И — 5 мкм Fig. 4. Light micrograph of Bolbolaimus brevis sp. nov., males (А, В, Г, Е, З, И, К) and female (Б, Δ, Ж, Α). А, Б – general view; В, Г, Δ – head; Е – anterior body end; Ж – vulva region; З, И – cloaca region; К, Α – tail. Scale bars: А, Б – 50 µm; Е, Ж, К, Α – 10 µm; В, Г, Δ, З, И – 5 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 4. Фотографии Bolbolaimus brevis sp. nov., самец (А, В, Г, Е, З, И, К) и самка (Б, Δ, Ж, Α). А, Б — общий виΑ; В, Г, Δ — гоΛова; Е — переΑний конец теΛа; Ж — теΛо в обΛасти вуΛьвы; З, И — теΛо в обΛасти кΛоаки; К, Α — хвост. Масштаб: А, Б — 50 мкм; Е, Ж, К, Α — 10 мкм; В, Г, Δ, З, И — 5 мкм Fig. 4. Light micrograph of Bolbolaimus brevis sp. nov., males (А, В, Г, Е, З, И, К) and female (Б, Δ, Ж, Α). А, Б – general view; В, Г, Δ – head; Е – anterior body end; Ж – vulva region; З, И – cloaca region; К, Α – tail. Scale bars: А, Б – 50 µm; Е, Ж, К, Α – 10 µm; В, Г, Δ, З, И – 5 µm
Fig. 2 in Genetic characterization and description of Leishmania (Leishmania) ellisi sp. nov.: a new human-infecting species from the USA
Fig. 2 Phylogenetic tree demonstrating the relative position of Leishmania sp. strain 218-L139 based on a concatenated sequence comprising several nuclear loci. Phylogenetic tree demonstrating the relative position of Leishmania strain 218-L139 (brown star) based on alignment of a concatenated sequence comprising the 18S rDNA, 28S rDNA, CKIIα, GAPDH, and RPOIILS nuclear sequences. The alignment contains 6577 positions from 33 taxa. The tree was built using maximum likelihood (1000 bootstrap replicates) and Bayesian
Fig. 1 in Genetic characterization and description of Leishmania (Leishmania) ellisi sp. nov.: a new human-infecting species from the USA
Fig. 1 Morphology of Leishmania strain 218-L139 promastigotes and amastigotes. Cultured Leishmania strain 218-L139 promastigotes as observed under DIC microscopy following growth in complete RPMI culture medium without gentamicin (A). Giemsa-stained touch preparation made from a cutaneous lesion, showing Leishmania strain 218-L139 amastigotes inside a mononuclear phagocyte in addition to free amastigotes (B). Giemsastained smear of cultured promastigotes of Leishmania strain 218-L139 grown in gentamicin-free complete RPMI medium (C)
Fig. 3 in Genetic characterization and description of Leishmania (Leishmania) ellisi sp. nov.: a new human-infecting species from the USA
Fig. 3 Phylogenetic tree demonstrating the relative position of Leishmania strain 218-L139 based on partial maxicircle genome sequences. Phylogenetic tree demonstrating the relative position of Leishmania strain 218-L139 (brown star) based on alignment of partial maxicircle genome sequences. The alignment contains 9471 positions from 67 taxa. The tree was built using maximum likelihood (1000 bootstrap replicates) and the TVM + F + I + G4 model, and Bayesian inference using the GTR + I + G model where the proportion of invariable sites was set to 0.1. Posterior probability values and bootstrap support are reported for each node (pp/bs). The tree was rooted with the Strigomonas/Blechomonas/Herpetomonas clade. The relative position of each Leishmania subgenus is shown to the right of the corresponding clades (Leishmania, Sauroleishmania, Viannia, Mundinia). The scale bar represents the number of substitutions per site
Fig. 2 in Description of Aleuropleurocelus sampsoni sp. nov. (Hemiptera: Aleyrodidae) from Tamaulipas, Mexico
Fig. 2. Aleuropleurocelus sampsoni Sánchez-Flores & Carapia-Ruiz sp. nov.: (a) abdominal segments; (b) longitudinal suture of the molt; (c) submarginal area; (d) vasiform orifice.
Fig. 3 in Description of Aleuropleurocelus sampsoni sp. nov. (Hemiptera: Aleyrodidae) from Tamaulipas, Mexico
Fig. 3. Aleuropleurocelus granulata (Sampson & Drews, 1941): (a) puparium in situ; (b) puparium mounted on slides; (c) puparium in situ, ventral view; (d) legs.
Fig. 1 in Description of Aleuropleurocelus sampsoni sp. nov. (Hemiptera: Aleyrodidae) from Tamaulipas, Mexico
Fig. 1. Aleuropleurocelus sampsoni Sánchez-Flores & Carapia-Ruiz sp. nov.: (a) puparium in situ; (b) puparium mounted on slides; (c) puparium in situ, ventral view; (d) legs.
Fig. 4 in Description of Aleuropleurocelus sampsoni sp. nov. (Hemiptera: Aleyrodidae) from Tamaulipas, Mexico
Fig. 4. Aleuropleurocelus granulata (Sampson & Drews, 1941): (a) abdominal segments; (b) longitudinal suture of the molt; (c) submarginal area; (d) vasiform orifice.
Fig. 5 in A cyst-forming coccidian with large geographical range infecting forest and commensal rodents: Sarcocystis muricoelognathis sp. nov.
Fig. 5 Phylogenetic reconstruction of the 18S rRNA gene tree of the novel Sarcocystis species and other tissue cyst-forming coccidia based on 1465 homologous positions of 40 aligned nucleotide sequences under the minimum evolution (ME) criterion; selected eimeriid coccidia served as outgroup. The new sequences of Sarcocystis sp. from China are highlighted by black symbols. Branch support values are shown for 1000 bootstrap replicates of three independent alignments with a site coverage of 95%. The shaded box highlights the taxa included in the so-called S. zuoi complex
Fig. 6 in A cyst-forming coccidian with large geographical range infecting forest and commensal rodents: Sarcocystis muricoelognathis sp. nov.
Fig. 6 ML analysis of the ITS1 region of Sarcocystis sp., S. zuoi and other species of the Sarcocystidae; members of the Toxoplasmatinae served as outgroup. Bootstrap branch support values are shown in triplicate, indicating results from three independent alignments and analyses.The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The analysis involved 204 homologous positions of 33 nucleotide sequences
Fig. 1 a–f in A cyst-forming coccidian with large geographical range infecting forest and commensal rodents: Sarcocystis muricoelognathis sp. nov.
Fig. 1 a–f Light microscopic and ultrastructural morphology of sarcocysts of Sarcocystis sp. in SD rats 5 months after inoculation with sporocysts isolated from rat snakes in Thailand. a Typical sporocyst from a fecal sample of Coelognathus radiatus; sporocysts from C. flavolineatus were identical in size and appearance; asterisk indicates single sporozoite. b Live sarcocyst, freed from muscle tissue; note the broad, palisade-like villar protrusions that could at times resemble those of Sarcocystis singaporensis with which this species can co-occur; however, the protrusions lack the basal stalks typical for the former species; the arrow highlights the septated compartments in the interior of the sarcocyst, and the inset shows a micrograph of live cystozoites freshly released from a cyst (arrowheads). c Typical structure of a cyst wall protrusion (isolate from C. flavolineatus); the arrows point to the electron-dense, knob-like structures of the primary cyst wall, whereby the knobs could apparently fuse to form an electron-dense borderline in larger protrusions (inset: arrowhead); also note the electron-light, thin layer of ground substance (GS) underneath the protrusions. d Typical cystozoites of the new species, which contained only two rhoptries (arrowheads) among relatively few micronemes (asterisks); additionally, the cystozoites exhibited vesicle-like structures in the anterior third of the cell containing electron-light, reticulate matter (arrow); the inset shows such a vesicle-like compartment at higher magnification, which was apparently not bound by a membrane (white arrow) and often located near micronemes (white asterisk); dense granules were present but rarely observed. e Interior and cyst wall of a mature sarcocyst (isolate from C. radiatus); metrocytes (asterisks) exclusively divided by endodyogeny, producing only two cystozoites (CZ). f Full-length section through a 15-µm-long protrusion of the sarcocyst wall; note that larger protrusions often occurred close to the tips of a cyst and showed a base with folds. AP, apicoplast; MI, mitochondrion; NU, nucleus; PT, villar protrusions
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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.