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Fig. 1 in First report of Crenosoma vulpis in Africa and Eucoleus aerophilus in Algeria
Fig. 1. Morphological characteristics of Crenosoma vulpis male. a) The anterior part of the nematode showing specific cuticular folds; b) the general appearance of the male nematode; c) posterior end of the worm showing the copulatory bursa and the spicules.
Fig. 3 in First report of Sarcocystis spp. (Apicomplexa, Sarcocystidae) in Lagostomus maximus (Desmarest, 1917) (Rodentia, Chinchillidae) in Argentina
Fig. 3. Phylogenetic tree of coxI using the Neighbor-Joining method. Sequences obtained from muscles samples of Lagostomus maximus (VC46, VC44, VC36, VC38, and VC43) form a separate clade of other Sarcocystis species with a sister clade formed by S. canis and Sarcocystis sp. sequences.
Fig. 1 in First report of Sarcocystis spp. (Apicomplexa, Sarcocystidae) in Lagostomus maximus (Desmarest, 1917) (Rodentia, Chinchillidae) in Argentina
Fig. 1. Photograph at inverted microscope at 40× magnification of a sarcocyst portion from a plains viscacha muscle pool.
Fig. 2 in First report of Sarcocystis spp. (Apicomplexa, Sarcocystidae) in Lagostomus maximus (Desmarest, 1917) (Rodentia, Chinchillidae) in Argentina
Fig. 2. Phylogenetic tree of 18S rRNA using the Neighbor-Joining method. Sequences obtained from muscles samples and individual cysts of Lagostomus maximus (VC46_1_cyst_B, VC46, VC44, VC38, and VC43) form a separate clade of other Sarcocystis species and S. nesbitti sequences formed a sister branch.
Fig. 3 in Co-infection of Echinococcus equinus and Echinococcus canadensis (G6/7) in a gray wolf in Turkey: First report and genetic variability of the isolates
Fig. 3. The haplotype network for the mt-CO1 gene (815 bp) of E. equinus. The size of the circles is proportional to the frequency of each haplotype. The number of mutations separating haplotypes is indicated by dash marks. The host diversity of haplotypes is shown in different colors. Hap: Haplotype.
Fig. 1 in First report on the molecular detection of Enterocytozoon bieneusi in livestock and wildlife around Qinghai Lake in the Qinghai-Tibetan Plateau area, China
Fig. 1. Phylogenetic tree of E. bieneusi isolates and reference based on ITS region sequence of small-subunit ribosomal RNA (SSU rRNA) genes.
Fig. 4 in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 4. Haplotype network of G1/G3 haplotypes identified on the basis of partial nad5 gene (628 bp). The G1 isolates obtained in this study (Hap01-Hap04), G3 isolates (Hap05, Hap06). Hatch marks represent the number of mutations between the haplotypes and the size of circle corresponds to the frequency of each haplotype in the population. Haplotypes formed by the isolates obtained in this study are marked with an asterisk.
Fig. 3. Haplotype network for E in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 3. Haplotype network for E. canadensis (G6/G7) using cox1 gene (616 bp) sequences of different countries. The E. canadensis (G6/G7) isolate obtained in this investigation (Hap_01) and the sequences identified as G7 in the Genbank database were utilized. Circle size relative to haplotype data set frequency. Each hatch mark is representative of one nucleotide change. Haplotypes formed by the isolates obtained in this study are marked with an asterisk.
Fig. 1 in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 1. Hydatid cyst image obtained from the lung (A) and liver (B) and C. tenuicollis (C,D) image obtained from its mesentery of wild boar.
Fig. 2. Haplotype network constructed using cox1 in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 2. Haplotype network constructed using cox1 (744 bp) gene sequences of T. hydatigena. Seven haplotypes formed by the T. hydatigena isolates obtained in this study: (Hap 1-Hap 7). Circle size relative to haplotype data set frequency. Each hatch mark is representative of one nucleotide change. Haplotypes formed by the isolates obtained in this study are marked with an asterisk.
FIGURE 3 in First report of Quaternary mammals from the Qalehjough area, Lut Desert, Eastern Iran
FIGURE 3. Stratigraphic section and the situation of fossil occurrence in Qalehjough fossil site (drawn by Narges Hashemi).
FIGURE 2. 1 in First report of Quaternary mammals from the Qalehjough area, Lut Desert, Eastern Iran
FIGURE 2. 1, Map depicting major cities and local villages around the Qalehjough fossil site. 2, Photograph of the fossil bearing sediments (photographed by Narges Hashemi).
FIGURE 1 in First report of Quaternary mammals from the Qalehjough area, Lut Desert, Eastern Iran
FIGURE 1. Locations of the Qalehjough fossil site, near Faizabad of Khorassan Razavi province, and other Quaternary fossil sites in Iran. Fossil vertebrate assemblages from these sites consist of following elements (E = Equus, R = Rhinocerotidae, and C = Caprinae): Qalehjough (E, R, C), Tapeh Naderi (E, C), Shadiakh (E, C), Qazvin (E, R, C), Saveh (E, R), Luristan (E), Qaleh bozi (E, R, C), Kermanshah (E, R), Shahreza (E), and Shahre Soukhteh (E).
FIGURE 4 in First report of Quaternary mammals from the Qalehjough area, Lut Desert, Eastern Iran
FIGURE 4. Photographs of selected vertebrate fossils from the Qalehjough fossil site. 1-2, a right P4 of Stephanorhinus cf. kirchbergensis (QHJ-45) in lateral (1) and occlusal (2) views. 3-5, three incisors of Equus (QHJ-12–14) in lateral views. 6-7, a right M3 of Equus (QHJ-22) in lateral (6) and occlusal (7) views. 8-9, a left M3 of Equus (QHJ-42) in lateral (8) and occlusal (9) views. 10, a first phalange of Sus (QHJ-37) in lateral view. 11, a left mandible of Ovis aries with P4 (QHJ-44) in lateral view. 12-13, a left M2 of O. aries (QHJ-5) in lateral (12) and occlusal (13) views. 14, a left mandible of Bos (QHJ-1) in lateral view. 15-16, a horn core (mesiodistal part) of Bos (QHJ-26) in internal (15) and external (16) views. 17-18, a left M2 of Gazella (QHJ-23) in lateral (17) and occlusal (18) views. Scale bars equal 1 mm.
FIGURE 15 in Deep-sea dragonfishes (Teleostei: Stomiiformes) collected from off northeastern Brazil, with a review of the species reported from the Brazilian Exclusive Economic Zone
FIGURE 15 | A. Eustomias bibulbosus, NPM 4642, 87 mm SL; B. Eustomias braueri, NPM 4816, 56 mm SL; C. Eustomias brevibarbatus, NPM 4646, 95 mm SL; D. Eustomias enbarbatus, NPM 4819, 60 mm SL; E. Eustomias minimus, NPM 4881, 69 mm SL; F. Eustomias schmidti, NPM 4882, 68 mm SL. Scale bars = 10 mm.
FIGURE 9 in Deep-sea dragonfishes (Teleostei: Stomiiformes) collected from off northeastern Brazil, with a review of the species reported from the Brazilian Exclusive Economic Zone
FIGURE 9 | A. Borostomias elucens, NPM 4299, 196 mm SL; B. Heterophotus ophistoma, NPM 4400, 223 mm SL. Scale bars = 10 mm.
FIGURE 16 in Deep-sea dragonfishes (Teleostei: Stomiiformes) collected from off northeastern Brazil, with a review of the species reported from the Brazilian Exclusive Economic Zone
FIGURE 16 | A. Grammatostomias dentatus, NPM 3184, 114 mm SL; B. Grammatostomias ovatus, NPM 3191, 67 mm SL; C. Leptostomias gladiator, NPM 4782, 83 mm SL. Scale bars = 10 mm.
FIGURE 8 in Deep-sea dragonfishes (Teleostei: Stomiiformes) collected from off northeastern Brazil, with a review of the species reported from the Brazilian Exclusive Economic Zone
FIGURE 8 | A. Astronesthes atlantica, NPM 4019, 32 mm SL; B. Astronesthes gemmifer, NPM 4799, 146 mm SL; C. Astronesthes gudrunae, NPM 4802, 111 mm SL; D. Astronesthes richardsoni, NPM 3194, 71 mm SL; E. Astronesthes similus, NPM 4811, 75 mm SL. Scale bars = 10 mm.
FIGURE 6 in Deep-sea dragonfishes (Teleostei: Stomiiformes) collected from off northeastern Brazil, with a review of the species reported from the Brazilian Exclusive Economic Zone
FIGURE 6 | A. Ichthyococcus polli, NPM 4119, 51 mm SL; B. Phosichthys argenteus, NPM 4560, 64 mm SL; C. Pollichthys mauli, NPM 3290, 38 mm SL; D. Vinciguerria nimbaria, NPM 3305, 27 mm SL. Scale bars = 10 mm.
FIGURE 11 in Deep-sea dragonfishes (Teleostei: Stomiiformes) collected from off northeastern Brazil, with a review of the species reported from the Brazilian Exclusive Economic Zone
FIGURE 11 | A. Stomias danae, NPM 4768, 95 mm SL; B. Stomias longibarbatus, NPM 4598, 173 mm SL. Scale bars = 10 mm.
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.