Find research datasets worth reusing

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 in EVALUATION OF THE EFFECTIVENESS OF USING A UNIVERSAL METHOD FOR ISOLATING GENOMIC dsDNA BY SALTING OUT TECHNIQUE ACCORDING TO THE S.M. ALJANABI AND I. MARTINEZ PROTOCOL FOR YEAST SACCHAROMYCES CEREVISIAE

Figure 2. Quantification of extracted Saccharomyces cerevisiae DNA by UVVis Spectrophotometry (DNA samples: 1–15).

opencc-by-4.0Dec 2011View details →

Fig. 3. Agarose gel image Fig. 4 in Optimization Of Dna Extraction Protocol For Dna Isolation From Air-Dried Collection Material For Further Phylogenetic Analysis (Coleoptera: Carabidae)

Fig. 3. Agarose gel image Fig. 4. Agarose gel image (successful PCR amplification) (failed PCR amplification) M: marker (bp) M: marker (bp) A1: Agonum fuliginosum Panzer, 1809 A: Agonum fuliginosum Panzer, 1809 A2: Agonum thoreyi Dejean, 1828 O: Omophron aequale aequale Morawitz, 1863 O: Omophron aequale aequale Morawitz, 1863 N: Notiophilus semistriatus Say, 1823 N: Notiophilus semistriatus Say, 1823 Nk: negative control. Nk: negative control.

opencc-by-4.0Dec 2011View details →

Fig. 1 in Optimization Of Dna Extraction Protocol For Dna Isolation From Air-Dried Collection Material For Further Phylogenetic Analysis (Coleoptera: Carabidae)

Fig. 1. Photo of Omophron aequale jacobsoni Fig. 2. Photo of Omophron aequale jacobsoni Semenov, 1922 before incubation. Semenov, 1922 after 16 h (56°C) incubation time in tissue lysis buffer with proteinase K.

FIGURE 15 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 15. Allometric shape variation in the M1-3 of Sparassodonta as shown by the Procrustes-transformed coordinates. (A) Superimposed differences in allometric shape at the smallest (black) and largest (gray) extremes of the size range of the dataset. (B-C) Deformation grids showing differences in allometric shape variation between the sample average and (B) minimum size and (C) maximum size. Differences between loci are magnified by a factor of 2 to better illustrate patterns of variation.

FIGURE 6 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 6. Inter-locus variation in the M1-3 of Sparassodonta as shown by the Procrustes-transformed coordinates of the geometric morphometric analysis. (A) Superimposed differences between tooth loci in the Procrustes-transformed coordinates of the average shape of M1 (large gray circles) and M3 (small black circles). The other three images show deformation grids from the average shape of all 114 examined specimens relative to the average shape of (B) M1, (C) M2, and (D) M3. Differences between loci are magnified by a factor of 3 to better illustrate patterns of variation.

FIGURE 7 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 7. Plot of shape data (as regression score; see Drake and Klingenberg, 2008 for definition) versus natural log centroid size for all teeth of known locus in the trigon + talon dataset, showing the allometric signal in the data and the slight clustering of the teeth by locus. The extreme outlier in centroid size is the M3 of Proborhyaena gigantea, which is very large compared to the other teeth examined.

FIGURE 11 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 11. Similar to Figure 10, but with the trigon-only dataset. Plot of the first two canonical variates (CVs) of the all-taxon, trigon-only discriminant analysis with tooth locus coded by symbol and incorrectly-classified specimens uncolored. Convex hulls represent morphospace occupied by each tooth locus.

FIGURE 3 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 3. Right upper molar row of Borhyaena tuberata (MACN-A 6203), showing the change in absolute and relative sizes of the paracone and metacone from M1-3 and the relatively little inter-locus variation in stylar shelf morphology. Scale equals 5 mm.

FIGURE 2. Right M2 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 2. Right M2 of Acyon myctoderos (UATF-V-000926), a specimen close to the mean shape of the entire dataset, showing the morphological features of interest (A) and geometric morphometric landmarks and semilandmarks (B) used in this study. Anatomical abbreviations: alc, anterolabial cingulum (often extensive and continuous with preparaconular crista); cc, centrocrista; ef, ectoflexus; mco, metaconule; met, metacone; msl, metastylar lobe of stylar shelf; par, paracone; pco, paraconule; pmc, postmetacrista; ppc, preparacrista; pro, protocone; psl, parastylar lobe of stylar shelf; ss, stylar shelf; StA, stylar cusp A; StB, stylar cusp B. In B, squares represent fixed landmarks and circles represent semilandmarks.

FIGURE 16 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 16. (A) TPS deformation grid showing allometric shape variation extrapolated beyond the lower bounds of the present dataset by a factor of 3 compared to (B) a photograph of the M3 of Pediomys elegans (modified from Davis, 2007: fig. 3c). Scale equals 1 mm.

FIGURE 14 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 14. Visualization of shape changes in two Miocene borhyaenids that show little change between tooth loci. (A) M1 (gray) and M3 (black) of Borhyaena tuberata (MACN-A 6404) and (B) M2 (gray) and M3 (black) of Arctodictis sinclairi (AMNH 27909).

FIGURE 13. Superimposed landmark diagrams visualizing shape changes between M1 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 13. Superimposed landmark diagrams visualizing shape changes between M1 (large gray circles) and M3 (small black circles) of selected non-borhyaenid sparassodonts: (A) Allqokirus australis (MNHC 8267), (B) Patene coluapiensis (AMNH 28448), (C) Procladosictis anomala (MACN-A 10327), (D) Hondadelphys fieldsi (UCMP 37960), (E) Sipalocyon gracilis (AMNH 9254), (F) Lycopsis longirostrus (UCMP 38061), (G) Prothylacynus patagonicus (MACN-A 707), (H) Thylacosmilus atrox (MMP 1443).

FIGURE 8 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 8. Plot of teeth by locus on the first two principal components for the all-taxon, trigon + talon dataset, colorcoded as pertaining to either Borhyaenoidea, Hathliacynidae, or basal Sparassodonta.

FIGURE 10 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 10. Plot of the first two canonical variates (CVs) of the all taxon, trigon + talon discriminant analysis, with tooth locus coded by symbol and incorrectly-classified specimens uncolored. Convex hulls represent morphospace occupied by each tooth locus.

FIGURE 9 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 9. Plot of teeth by locus on the first two principal components for the all-taxon, trigon + talon dataset, colorcoded by relative grinding area (RGA) for that particular taxon. Gray symbols represent taxa for which RGA could not be measured.

FIGURE 17 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics

FIGURE 17. Comparison of the TPS deformation grids for the M3 of Procladosictis anomala (A) and the mean M3 shape for the entire sample exaggerated by a factor of 3 (B), both contrasted against the mean tooth shape for the entire sample.