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Fig. 5 in Peculiarities of Trypanosoma rangeli KP1(-) Strains Isolated from the Wild Rodent Phyllomys dasythrix (Santa Catarina, Brazil): Comparisons with T. rangeli KP1(+) strains and Trypanosoma lewisi (Kinetoplastea, Trypanosomatidae)
Fig. 5. kDNA minicircle amplicons presented by all KP1(+) and KP1(–) Trypanosoma rangeli strains examined in this study, and obtained by polymerase chain reaction using the primers 121/122. (M) molecular marker (100-bp DNA ladder).
Fig. 4 in Peculiarities of Trypanosoma rangeli KP1(-) Strains Isolated from the Wild Rodent Phyllomys dasythrix (Santa Catarina, Brazil): Comparisons with T. rangeli KP1(+) strains and Trypanosoma lewisi (Kinetoplastea, Trypanosomatidae)
Fig. 4. Isoenzyme profiles at IDH locus presented by KP1(+) and KP1(–) Trypanosoma rangeli strains and T. lewisi.
Fig. 3 in Peculiarities of Trypanosoma rangeli KP1(-) Strains Isolated from the Wild Rodent Phyllomys dasythrix (Santa Catarina, Brazil): Comparisons with T. rangeli KP1(+) strains and Trypanosoma lewisi (Kinetoplastea, Trypanosomatidae)
Fig. 3. Diagrammatic representation of the electrophoretic patterns of malate dehydrogenase (MDH), phosphoglucomutase (PGM), glucose phosphate isomerase (GPI) and malic enzyme (ME) displayed by KP1(–) and KP1(+) Trypanosoma rangeli strains, and T. lewisi.
Fig. 1 in Peculiarities of Trypanosoma rangeli KP1(-) Strains Isolated from the Wild Rodent Phyllomys dasythrix (Santa Catarina, Brazil): Comparisons with T. rangeli KP1(+) strains and Trypanosoma lewisi (Kinetoplastea, Trypanosomatidae)
Fig. 1. Camera lucida drawings of representative bloodstream trypomastigotes of Trypanosoma rangeli KP1(–) and KP1(+) strains from experimentally infected mice by metacyclic trypomastigotes grown in DMEM medium. The position of the nucleus in each trypomastigote is indicated by arrowheads. Parasites were from Giemsa-stained smears of each strain, as seen under optical microscopy (×1,000). In a trypomastigote of the strain SC-61 are indicated the reference points for taking measurements: anterior end (A), posterior end (P), nucleus (N) and free flagellum (F).
Fig. 2 in Peculiarities of Trypanosoma rangeli KP1(-) Strains Isolated from the Wild Rodent Phyllomys dasythrix (Santa Catarina, Brazil): Comparisons with T. rangeli KP1(+) strains and Trypanosoma lewisi (Kinetoplastea, Trypanosomatidae)
Fig. 2. Comparative growth in axenic cultures of Trypanosoma rangeli strains [KP1(–) and KP1(+)] and T. lewisi. Data (106 cells/μL) are the averages and the maximum growth from the values taken at the 4th, 7th, 10th, 13th, 17th and 20th days of cultivation in liver infusion-tryptose broth supplemented with 20% fetal calf serum (LIT-20) at 27.3 ± 0.4°C.
Figure 2. a in Fleas (Insecta: Siphonaptera) On Lithuania Small Rodents
Figure 2. a) Ctenophthalmus agyrtes, b) Megabothris turbidus, c) M. walkeri, d) Hystrichopsylla talpae
FIGURE 3 in Biostratigraphy and biochronology of late Cenozoic North American rodent assemblages
FIGURE 3. Examples of Microtus m1 morphology. A-C, Microtus pennsylvanicus (from Martin, 1990), D-F, Microtus paroperarius (from van der Meulen, 1978). ACC = anteroconid complex, BRA = buccal reentrant angle, LRA = lingual reentrant angle. Numbers in illustration D refer to triangle numbers.
FIGURE 1 in Biostratigraphy and biochronology of late Cenozoic North American rodent assemblages
FIGURE 1. Distribution of select pre-Rancholabrean Cenozoic rodent assemblages used to construct the database in Supplementary Material. 1 = Rancho el Ocote, MX; 2 = Concha, MX; 3 = Yepómera, MX; 4 = El Golfo, CA; 5 = Vallecito-Fish Creek sequence (e.g., Layer Cake, Arroyo Seco, Vallecito Creek), CA; 6 = San Pedro Valley sequence (e.g., Benson, Curtis Ranch, Duncan), AZ; 7 = Verde, AZ; 8 = McKay Reservoir, OR; 9 = Warren, CA; 10 = Panaca, NV; 11 = White Bluffs, WA; 12 = Kennewick, WA; 13 = Buckeye Creek, NV; 14 = Fish Springs Flat, NV; 15 = Grand View-Hagerman sequence (e.g., Grand View, Sand Point, Hagerman, Birch Creek, Froman Ferry), ID; 16 = Donnelly Ranch, CO; 17 = San Timoteo Badlands, CA; 18 = Wellington Hills, NV; 19 = Mesa del Sol, NM; 20 = Boyle Ditch, WY; 21 = Virden, NM; 22 = Ft. Selkirk, YT; 23 = El Casco, CA; 24 = SAM Cave, NM; 25 = Little Dell Dam, UT; 26 = Porcupine Cave, CO; 27 = Hansen Bluff, NM; 28 = Meade Basin reference section (see Figure 2 for all assemblages; includes Arlene's Ledge/Robin's Roost in OK), KS/NM; 29 = Little Sioux and Wright (new), IA; 30 = Cape Deceit, AL; 31 = Santee, NE; 32 = Mailbox, NE; 33 = Sand Draw area (Sand Draw, Zwiebel Channel), NE; 34 = Pipe Creek Sinkhole, IN; 35 = Hudspeth/Red Light, TX; 36 = Bull Draw/Deadman's Crk, TX; 37 = Red Corral, TX; 38 = Cita Canyon, TX; 39 = Blanco, TX; 40 = Vera, TX; 41 = Beck Ranch, TX; 42 = Fyllan Cave, TX; 43 = Conard Fissure, AK; 44 = Port Kennedy Cave, PA; 45 = Hanover Quarry, PA; 46 = Cumberland Cave, MD; 47 = Haile 15A, Haile 16A, FL; 48 = Inglis 1A/1C, FL; 49 = Hamilton Cave, WV; 50 = White Rock, KS; 51 = Dixon, KS, 52 = Leisey Shell Pit, FL, 53 = Hoye Canyon, NV.
FIGURE 2 in Biostratigraphy and biochronology of late Cenozoic North American rodent assemblages
FIGURE 2. Depositional basin framework on which chronological ordering of assemblages (= localities) in Supplementary Material is mostly based. See Supplementary Material and text for full rodent communities, locality data, and information sources. LSD = lowest stratigraphic datum, HSD = highest stratigraphic datum. LSDs and HSDs are regional basin limits, but may also represent global limits (highest or lowest records anywhere in North America). Esr = estimated age based on sedimentation rate from Hart and Brueseke, 1999), ft = fission track date from Walkup et al., 2016), CMZ = Cenozoic Mammal Zone, xxx... = dated volcanic ash beds. Continued on next page.
FIGURE 4 in Biostratigraphy and biochronology of late Cenozoic North American rodent assemblages
FIGURE 4. Plot of arvicoline species richness on ordinate against CMZ midpoints on abscissa. Numbers on graph are CMZs. CMZ 1 omitted.
FIGURE 12 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 12. Three-dimensional models visualizing the sequence of the wear stages (A-E) for the m1 of Pliospalax. Occlusal view. (1) anterosinusid, (2) protosinusid, (3) sinusid, (4) posterosinusid, (5) mesosinusid.
FIGURE 11 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 11. Three-dimensional model visualizing the sequence of the wear stages (11.1-11.9) for the left m1 of Spalax microphthalmus (REG 22729) from Hungary. Labial and occlusal view. The scale bars apply to all panels of the figure.
FIGURE 6 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 6. Three-dimensional model visualizing the sequence of the wear stages (6.1-6.12) for the m1 of Pliospalax tourkobouniensis (TB1-901), from the locality of Tourkobounia-1 in Greece (De Bruijn and Van der Meulen, 1975). Labial and occlusal view. The scale bars apply to all panels of the figure.
FIGURE 5 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 5. Three-dimensional model visualizing the sequence of the wear stages (5.1-5.9) for the holotype (m1) of Pliospalax tourkobouniensis (TB1 481), from the locality of Tourkobounia-1 in Greece (De Bruijn and Van der Meulen, 1975). Labial and occlusal view. The scale bars apply to all panels of the figure.
FIGURE 2 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 2. Three-dimensional model visualizing the sequence of the wear stages (2.1-2.12) for the m1 of Pliospalax macoveii (ACA 859) from the locality of Çalta in Turkey (Şen, 1977). Labial and occlusal view. Inverted figure of the specimen. The scale bars apply to all panels of the figure.
FIGURE 3 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 3. Three-dimensional model visualizing the sequence of the wear stages (3.1-3.12) for the right m1 of Pliospalax macoveii (ACA 881) from the locality of Çalta in Turkey (Şen, 1977). Labial and occlusal view. Inverted figure of the specimen. The scale bars apply to all panels of the figure.
FIGURE 8 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 8. Three-dimensional model visualizing the sequence of the wear stages (8.1-8.9) for the right m1 of Spalax microphthalmus (REG 22726) from Romania. Labial and occlusal view. Inverted figure of the specimen. The scale bars apply to all panels of the figure.
FIGURE 10 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 10. Three-dimensional model visualizing the sequence of the wear stages (10.1-10.12) for the right m1 of Spalax microphthalmus (REG 22729) from Hungary. Labial and occlusal view. Inverted figure of the specimen. The scale bars apply to all panels of the figure.
FIGURE 9 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 9. Three-dimensional model visualizing the sequence of the wear stages (9.1-9.9) for the left m1 of Spalax microphthalmus (REG 22726) from Romania. Labial and occlusal view. The scale bars apply to all panels of the figure.
FIGURE 4 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 4. Three-dimensional model visualizing the sequence of the wear stages (4.1-4.12) for the left m1 of Pliospalax macoveii (ACA 881) from the locality of Çalta in Turkey (Şen, 1977). Labial and occlusal view. The scale bars apply to all panels of the figure.
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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.