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Fig. 5 in Rodentolepis microstoma isolated from different species of Sigmodontinae rodents (Rodentia: Cricetidae) in the Cuenca del Plata, Argentina: Morphological aspects and molecular characterization
Fig. 5. Phylogenetic tree of Rodentolepis spp. (Hymenolepididae: Cestoda) based on concatenated cox1 mitochondrial and ITS1 ribosomal DNA. Phylogenetic tree inferred using Bayesian method. Maximum Likelihood bootstrap values of clades are listed first, followed by Bayesian Posterior Probabilities respectively, for clade frequencies exceeding 65%.
Fig. 4 in Rodentolepis microstoma isolated from different species of Sigmodontinae rodents (Rodentia: Cricetidae) in the Cuenca del Plata, Argentina: Morphological aspects and molecular characterization
Fig. 4. Phylogenetic tree of Rodentolepis spp. (Hymenolepididae: Cestoda) based on cox1 mitochondrial DNA. Phylogenetic tree inferred using Bayesian method. Maximum Likelihood bootstrap values of clades are listed first, followed by Bayesian Posterior Probabilities respectively, for clade frequencies exceeding 65%.
Fig. 1 in Rodentolepis microstoma isolated from different species of Sigmodontinae rodents (Rodentia: Cricetidae) in the Cuenca del Plata, Argentina: Morphological aspects and molecular characterization
Fig. 1. Morphological features of Rodentolepis microstoma: (A, D, G, J) scolex and rostellar hooks; (B, E, H, K) mature proglottids; (C, F, I, L) egg from different host species, (A–C) Akodon; (D–F) Necromys; (G–I) Thaptomys; (J–L) Oxymycterus.
Fig. 3 in Rodentolepis microstoma isolated from different species of Sigmodontinae rodents (Rodentia: Cricetidae) in the Cuenca del Plata, Argentina: Morphological aspects and molecular characterization
Fig. 3. Phylogenetic tree of Rodentolepis spp. (Hymenolepididae: Cestoda) based on ITS1 mitochondrial DNA. Phylogenetic tree inferred using Bayesian method. Maximum Likelihood bootstrap values of clades are listed first, followed by Bayesian Posterior Probabilities respectively, for clade frequencies exceeding 65%.
Fig. 4 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. 4. The haplotype network for the mt-CO1 gene (815 bp) of E. canadensis (G6/7). 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. 2 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. 2. Phylogenetic tree of Echinococcus granulosus s.l. isolates generated using mt-CO1 gene sequences (815 bp). The phylogenetic tree was constructed using the Maximum Likelihood method and TN93 + G model. Evolutionary analyses were conducted in MEGA X. For each reference sequence, the GenBank accession number and species name are listed below: MN787562 (E. equinus), KY766905 (E. equinus), KP161210 (E. equinus) AB786665 (E. equinus) AF346403 (E. equinus), KX010854 (E. canadensis) MK321260 (E. canadensis) KX010856 (E. canadensis), AB893263 (E. canadensis), AB777923 (E. canadensis), MK165232 (E. ortleppi), MT072979 (E. granulosus s.s.), NC_044548 (E. granulosus s.s.), MG672293 (E. granulosus s.s.), KT001423 (E. multilocularis), AY684274 (T. saginata). ■: E. canadensis (G6/7) isolates; ▴: E. equinus isolates.
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. 2 in Identification of a new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea Gyrodactylidae) isolated from Diptychus maculatus in Yarkand River, Xinjiang, China
Fig. 2. Line drawings of the haptoral structures of Gyrodactylus diptychi n. sp. (A & B) Hamulus-bar complex, (C) Hamuli (HA), (D) Male copulatory organ (MCO),(E) Dorsal bar (DB), (F) Ventral bar (VB), (G) Marginal hook (MH), (H) Marginal hook sickle(MHS).
Fig. 1 in Identification of a new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea Gyrodactylidae) isolated from Diptychus maculatus in Yarkand River, Xinjiang, China
Fig. 1. Light micrographs of Gyrodactylus diptychi n. sp. (A) Hamulus-bar complex, (B) Hamuli (HA), (C) Male copulatory organ (MCO), (D) Dorsal bar (DB), (E) Ventral bar (VB), (F) Marginal hook (MH), (G) Marginal hook sickle(MHS).
Fig. 2 in Morphological and molecular characterization of parabasilids isolated from ex situ nonhuman primates and their keepers at different institutions in Brazil
Fig. 2. Phylogenetic analysis of a 100 bp fragment of the ITS variable region by the maximum likelihood test and the Kimura 2-parameter (K2P) evolutionary model of parabasilids isolated from samples of ex situ nonhuman primates (NHPs) and their keepers at different institutions in Brazil. Tree not rooted.
Fig. 5 in Identification of a new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea Gyrodactylidae) isolated from Diptychus maculatus in Yarkand River, Xinjiang, China
Fig. 5. The phylogenetic tree constructed by the BI and ML methods based on the ITS1-5.8S-ITS2 rDNA sequences from selected Gyrodactylus species. Numbers along branches represent Bayesian posterior probability/ML bootstrap support.
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.
Fig. 3 in Identification of a new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea Gyrodactylidae) isolated from Diptychus maculatus in Yarkand River, Xinjiang, China
Fig. 3. Marginal hook sickles of Gyrodactylus diptychi n. sp.; G. hemivicinus from Gusev (1985); G. kafirniganensis from Gusev (1985); G. marjami from Gusev (1985); G. montanus from Gusev (1985); G. narzikulovi from Gusev (1985); G. seravshani from Gusev (1985); G. vicinus from Gusev (1985); G. aksuensis from Gusev (1985); G. tokobaevi from Gusev (1985); G. dzhalilovi from Gusev (1985); G. editus from Gusev (1985); G. gymnodiptychi from Zhang et al., 2023; Scale bars: 20 μm.
Fig. 4 in Identification of a new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea Gyrodactylidae) isolated from Diptychus maculatus in Yarkand River, Xinjiang, China
Fig. 4. Morphological comparison of (A) Gyrodactylus diptychi n. sp., (B) Gyrodactylus hemivicinus, (C) Gyrodactylus kafirniganensis, and (D) Gyrodactylus montanus.
Fig. 3. T. brumpti trophozoite isolates obtained from A in Morphological and molecular characterization of parabasilids isolated from ex situ nonhuman primates and their keepers at different institutions in Brazil
Fig. 3. T. brumpti trophozoite isolates obtained from A. trivirgatus stool samples were subjected to rapid Panoptic staining kit (A–D). A. Trophozoite with three flagella visible in the anterior region (*) and a rounded nucleus (black arrow). B. Trophozoite with prominent axostyle in the posterior region (black arrow). C. Trophozoite with three flagella visible in the anterior region (black *). D. Trophozoite with a rounded body and visible undulating membrane (black arrow). E. Human isolate of Tetratrichomonas sp. F. T. batrachorum isolated from L. chrysomelas with many vacuoles inside the cell (white *). G. P. hominis isolated from S. collinsi with clearly visible axostyle (white *) and undulating membrane. H. H. hampli trophozoite with three flagella detected in howler monkey (A. guariba), surrounded by bacteria (black arrow). Maginification: 1000x.
Fig. 1. Maximum likelihood tree generating from a 399 in Isolation and Characterization of Polymorphic Microsatellite Loci for Caridina cantonensis and Transferability Across Eight Confamilial Species (Atyidae, Decapoda)
Fig. 1. Maximum likelihood tree generating from a 399-bp long COI dataset (GenBank accession no. MH176649-MH176993). SH-alrt/ bootstrap support values are indicated at major nodes. Each coloured notation represents one species.
FIGURE 18. Diplacanthus tenuistriatus isolated shoulder girdle complexes. 1–4, NMS G.2014.15.21 in The diplacanthid fishes (Acanthodii, Diplacanthiformes, Diplacanthidae) from the Middle Devonian of Scotland
FIGURE 18. Diplacanthus tenuistriatus isolated shoulder girdle complexes. 1–4, NMS G.2014.15.21 from Marwick, Orkney: 1, external surface of scapulocoracoid, pectoral fin spine, pinnal plate and admedian spine; 2, admedian spine; 3, 4, scale-like ornament on pinnal plate; 5, NMS G.2014.15.22 from Marwick, Orkney, internal surface; 6–9, transverse sections of NMS G.2014.4.20 from Marwick, Orkney: 6, pinnal plate; 7, multiple odontode on plate; 8, scalelike ornament; 9, transverse section through pinnal plate, pectoral fin spine base, scapulocoracoid and perichondral bone sheet; 10, 11, NMS G.2014.4.27 from Flashes, Hoy, Orkney, transverse section through base of admedian spine and inner perichondral bone sheet; 10, whole width; 11, scale-like ornament in groove. Scale bars equal 1 cm in 1, 5; 5.0 mm in 2; 1.0 mm in 3, 4, 6; 0.5 mm in 9, 10; 0.1 mm in 7, 8, 11; 0.05 mm in 4.
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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.