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824 results for “Discrimination”
Fig. 1 in Geometric morphometric on a new species of Trichodinidae. A tool to discriminate trichodinid species combined with traditional morphology and molecular analysis
Fig. 1. Microphotographs of Trichodina bellottii n. sp. from Austrolebias bellottii. (A–D) Adhesive disc after dry silver impregnation. E) Ciliature. (F) Macronucleus with methylene-blue staining. Scale bars: 20 μm.
Sex-dependent discrimination learning in lizards: a meta-analysis
<p>Raw data and R code used for analysis and to create plots</p>
Data for the publication "Rare Earth Elements in oyster shells: provenance discrimination and potential vital effects"
<p>Rare Earth Elements (REE) and yttrium measurements from modern and archaeological oyster shells collected by LA-ICP-MS. This dataset is used in the publication 'Rare Earth Elements in oyster shells: provenance discrimination and potential vital effects'.</p>
Figure 1 in Comparison of two morphometric methods for discriminating honey bee (Apis mellifera L.) populations in Turkey
Figure 1. Sampling locations in Turkey (Thrace: 1–2; Aegean: 3; Central Anatolia/ Mediterranean: 4–11; Southeastern Anatolia: 12–13; Northeastern Anatolia: 14–15).
Text-fig. 9. Sex estimation of Moča skull (Komárno district, southern Slovakia), linear discriminant analysis using Henke's Late Upper Palaeolithic and Mesolithic database (n = 129, f = 46, m = 83), as well as according to recent Howells's database (n = 2524, f = 1156, m = 1368) with variables M1 (GOL) and M45 (ZYB). in A Late Upper Palaeolithic Skull From Moča (The Slovak Republic) In The Context Of Central Europe
Text-fig. 9. Sex estimation of Moča skull (Komárno district, southern Slovakia), linear discriminant analysis using Henke's Late Upper Palaeolithic and Mesolithic database (n = 129, f = 46, m = 83), as well as according to recent Howells's database (n = 2524, f = 1156, m = 1368) with variables M1 (GOL) and M45 (ZYB).
Text-fig. 10. Regional affinity of the Moča skull (Komárno district, southern Slovakia), linear discriminant analysis using the Henke's Late Upper Palaeolithic and Mesolithic database (Europe, n = 76) with variables M1 (GOL), M5 (BNL), M8 (XCB), M40 (BPL), W – West Europe, CE – Central-East Europe, S – South Europe. in A Late Upper Palaeolithic Skull From Moča (The Slovak Republic) In The Context Of Central Europe
Text-fig. 10. Regional affinity of the Moča skull (Komárno district, southern Slovakia), linear discriminant analysis using the Henke's Late Upper Palaeolithic and Mesolithic database (Europe, n = 76) with variables M1 (GOL), M5 (BNL), M8 (XCB), M40 (BPL), W – West Europe, CE – Central-East Europe, S – South Europe.
Figure 3 in Application of multifactorial discriminant analysis in the morphostructural differentiation of wild and cultured populations of Vieja Azul (Andinoacara rivulatus)
Figure 3. Cluster from Mahalanobis distances for cultured and wild populations of both sexes. HP: Cultured females; HS: wild females; MP: cultures males; MS: wild males.
Figure 2 in Application of multifactorial discriminant analysis in the morphostructural differentiation of wild and cultured populations of Vieja Azul (Andinoacara rivulatus)
Figure 2. Plot of the individual observation discriminant scores obtained with the canonical discriminant function. HP: Cultured females; HS: wild females; MP: cultures males; MS: wild males.
Figure 1 in Application of multifactorial discriminant analysis in the morphostructural differentiation of wild and cultured populations of Vieja Azul (Andinoacara rivulatus)
Figure 1. (a) Location of 25 anatomic landmark points designed on the left-side view of Andinoacara rivulatus; (b) 32 truss characters making up a truss network. 1- Commissure of the mouth; 2- most cranial point of the upper premaxilla; 3- origin of pelvic fin; 4- origin of dorsal fin; 5- origin of anal fin; 6- most cranial point of the base of the tenth spine of the dorsal fin; 7- ending of anal fin; 8- ending of dorsal fin; 9- ventral origin of caudal fin; 10- dorsal origin of caudal fin; 11- most cranial point of caudal peduncle; 12- most caudal point of caudal peduncle; 13- ending of pectoral fin; 14- end of operculum; 15- cranial edge of the eye; 16- caudal edge of the eye; 17- preoccipital (most posterior aspect of neurocranium); 18- below operculum; 19- origin of pectoral fin; 20- lower end of the head; 21- anal opening; 22- most cranial point of the lower premaxilla; 23- ending of 1st dorsal fin ray; 24- ending of the last anal fin ray; 25- ending of the pelvic fin radius.
Figure 6 in Discrimination of the sister hedgehog species Erinaceus concolor and E. roumanicus (Erinaceomorpha: Mammalia): a geometric morphometric approach
Figure 6. Multivariate regression analysis of shape variables vs centroid size of the dorsal cranium (closed circle: E. concolor, n = 39; open circle: E. roumanicus, n = 10).
Figure 4 in Discrimination of the sister hedgehog species Erinaceus concolor and E. roumanicus (Erinaceomorpha: Mammalia): a geometric morphometric approach
Figure 4. PCA scatter plot graphics showing the variations in the mandible (closed circle: E. concolor, n = 54; open circle: E. roumanicus, n = 14) with warped outline drawings describing shape changes along the PC1 axis for each species.
Figure 5 in Discrimination of the sister hedgehog species Erinaceus concolor and E. roumanicus (Erinaceomorpha: Mammalia): a geometric morphometric approach
Figure 5. Histograms of the crossvalidation results. a. Dorsal surface of crania, b. Right side of mandible. Red bars: E. concolor; blue bars: E. roumanicus.
Fig. 3 in Isotopic discrimination and persistence of the C marker in adults of Anastrepha fraterculus (Diptera: Tephritidae) Brazilian-1 morphotype
Fig. 3. Stable carbon isotopic signature of Anastrepha fraterculus adults switched from different adult diets (sugar, mixture of sugar plus hydrolyzed yeast, or Gainesville diet) to apple (C3-based diet) over time.
Fig. 2 in Isotopic discrimination and persistence of the C marker in adults of Anastrepha fraterculus (Diptera: Tephritidae) Brazilian-1 morphotype
Fig. 2. Stable carbon isotopic signature of Anastrepha fraterculus adults switched from papaya slices (C3-based adult diet) to sugar (C4-based adult diet) over time.
Fig. 8 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 8. Morphological features distinguishing the distal portion of the humerus of Rangifer tarandus (A) and Cervus elaphus (B), in anterior (A1, B1), distal (A2,B2), and posterior (A3,B3) views (modified from Breda 2005).
Fig. 7 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 7. Morphological features distinguishing the proximal portion of the humerus of Rangifer tarandus (A) and Cervus elaphus (B) (modified from Pales and García 1981).
Fig. 6 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 6. Scatterplots of different combinations of scapular measurements and indices for Rangifer tarandus and Cervus elaphus from Kiputz IX (southern Pyrenees, Spain), Late Pleistocene. Abbreviations: GLP, greatest anteroposterior length of the glenoid process; LG, greatest anteroposterior length of the glenoid cavity; SLC, minimum diameter of the scapular neck.
Fig. 3 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 3. Osteological measurements of the scapula (A, B) and the humerus (C, D) (modified from Weinstock 2000a). All drawings are based on Rangifer tarandus.
Fig. 4 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 4. Morphological features distinguishing the scapulae of the cervid mammals Rangifer tarandus, BGG KI-IX.2D.39.618 (A) and Cervus elaphus, BGG KI-IX.2C.28.142 (B), from Kiputz IX (southern Pyrenees, Spain), Late Pleistocene, in lateral (A 1, B 1) and distal (A 2, B 2) views; α, the angle formed by the glenoid cavity and the supraglenoid tubercle.
Fig. 9 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 9. Scatterplot of the greatest breadth of the trochlea (BT) vs. the depth of the distal epiphysis (Dd) of the humerus of Rangifer tarandus and Cervus elaphus from Kiputz IX and other European sites.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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