Find research datasets worth reusing

opencc-by-4.0Dec 2022View details →

Рис. 1. Ctenoceratoda tancrei, бабочки из разΛичных ΛокаΛитетов: а, e — Киргизский хр., нац. парк «АΛа-Арча»; b, f — хр. ΔжумгаΛтоо, массив Сары-Кайкы; c, d, g, h — хр. МоΛΑо-Тоо, пер. Коро-Гоо. a–d — самцы, e–h — самки Fig. 1. Ctenoceratoda tancrei, the wing pattern variability: a, e — Kirghiz Mts., «Ala-Archa» national park; b, f — Dzhumgaltoo Mts., Sary-Kaiky gorge; c, d, g, h — Moldo-Too Mts., Koro-Goo Pass. a–d — males, e–h — females in Morphometric analysis of genitalia of Ctenoceratoda tancrei (Graeser, 1892) (Lepidoptera, Noctuidae)

Рис. 1. Ctenoceratoda tancrei, бабочки из разΛичных ΛокаΛитетов: а, e — Киргизский хр., нац. парк «АΛа-Арча»; b, f — хр. ΔжумгаΛтоо, массив Сары-Кайкы; c, d, g, h — хр. МоΛΑо-Тоо, пер. Коро-Гоо. a–d — самцы, e–h — самки Fig. 1. Ctenoceratoda tancrei, the wing pattern variability: a, e — Kirghiz Mts., «Ala-Archa» national park; b, f — Dzhumgaltoo Mts., Sary-Kaiky gorge; c, d, g, h — Moldo-Too Mts., Koro-Goo Pass. a–d — males, e–h — females

opencc-by-4.0Feb 2022View details →

Fig. 1 in Change Of Morphometric And Allometric Patterns On Wings Of Banded Demoiselle (Calopteryx Splendens) Males In Case Of Ecologically Different Watercourse Types

Fig. 1. The typical appearance of watercourse types in Northeast Hungary (A = creek, B = brook, C = stream, D = little river, E = medial river). (Photo: Miskolczi, M.)

opencc-by-4.0Feb 2022View details →

Fig. 5 in Change Of Morphometric And Allometric Patterns On Wings Of Banded Demoiselle (Calopteryx Splendens) Males In Case Of Ecologically Different Watercourse Types

Fig. 5. PCA with watercourse type, for fore and hind wing (1. component = 77.66%; 2. component = 11.70%) (filled symbols: fore wing, empty symbols: hind wing). Symbols:

opencc-by-4.0Feb 2022View details →

Fig. 2 in Change Of Morphometric And Allometric Patterns On Wings Of Banded Demoiselle (Calopteryx Splendens) Males In Case Of Ecologically Different Watercourse Types

Fig. 2. Measuring points on the right fore wing of Calopteryx splendens males (A = landmarks related to size and shape measurements, B = landmarks related to measurements on

opencc-by-4.0Oct 2019View details →

Рис. 1. Bryoxena centralasiae, изменчивость крыΛового рисунка: а, λ — Киргизский хр., нац. парк «АΛа-Арча»; в, г, з — хр. ΔжумгаΛтоо, массив Сары-Кайкы; д, к, м — хр. МоΛΑо-Тоо, пер. Коро-Гоо; б, е — Ферганский хр., пер. Урумбаш; ж, и — АΛайский хр., пер. ТаΛΑык Fig. 1. Bryoxena centralasiae, the wing pattern variability: а, λ — Kirghiz Mts., «Ala-Archa» national park; в, г, з — Dzhumgaltoo Mts., Sary-Kaiky gorge; д, к, м — Moldo-Too Mts., Koro-Goo Pass; б, е — Fergansky Mts., Urumbash Pass; ж, и — Alai Mts., Taldyk Pass in Morphometric Analysis Of The Genitalia Of (Staudinger, 1882) (Lepidoptera, Noctuidae)

Рис. 1. Bryoxena centralasiae, изменчивость крыΛового рисунка: а, λ — Киргизский хр., нац. парк «АΛа-Арча»; в, г, з — хр. ΔжумгаΛтоо, массив Сары-Кайкы; д, к, м — хр. МоΛΑо-Тоо, пер. Коро-Гоо; б, е — Ферганский хр., пер. Урумбаш; ж, и — АΛайский хр., пер. ТаΛΑык Fig. 1. Bryoxena centralasiae, the wing pattern variability: а, λ — Kirghiz Mts., «Ala-Archa» national park; в, г, з — Dzhumgaltoo Mts., Sary-Kaiky gorge; д, к, м — Moldo-Too Mts., Koro-Goo Pass; б, е — Fergansky Mts., Urumbash Pass; ж, и — Alai Mts., Taldyk Pass

Fig. 5 in A geometric morphometric study of the wing shapes of Pieris rapae (Lepidoptera: Pieridae) from the Qinling Mountains and adjacent regions: An environmental and distance-based consideration

Fig. 5. Hind wing shape variation (CV1: 50.41%; CV2: 15.49%). The colored circles in the image above represent the average discrete point center of populations; the number is the population ID. Thin-plate spline analysis results are shown by colored grid, which represents wing shape deformation. The numbers on the grid are landmarks of wings. Blue color denotes contraction between landmarks, and red color indicates expansion between landmarks. The North group and South group correspond to the boundary of Qinling Mountains as the boundary between northern and southern China.

Fig. 4 in A geometric morphometric study of the wing shapes of Pieris rapae (Lepidoptera: Pieridae) from the Qinling Mountains and adjacent regions: An environmental and distance-based consideration

Fig. 4. Forewing shape variation (CV1: 46.68%; CV2: 14.88%). The colored circles in the image above represent the average discrete point centers of populations; the number is the population ID. Thin-plate spline analysis results are shown by colored grid, which represents wing shape deformation. The numbers on the grid are landmarks of wings. Blue colored notes contraction between landmarks, and red color indicates expansion between landmarks. The North group and South group correspond to the boundary of Qinling Mountains as the boundary between northern and southern China.

Fig. 1 in A geometric morphometric study of the wing shapes of Pieris rapae (Lepidoptera: Pieridae) from the Qinling Mountains and adjacent regions: An environmental and distance-based consideration

Fig. 1. Distribution map of the P. rapae populations studied and the integrated physical regionalization (diverse environments) in the Qinling Mountains and adjacent regions. Note: The numbers represent the IDs of the populations; the circles and groups represent the populations divided by the cluster analysis from Fig. 6.

Fig. 3 in A geometric morphometric study of the wing shapes of Pieris rapae (Lepidoptera: Pieridae) from the Qinling Mountains and adjacent regions: An environmental and distance-based consideration

Fig. 3. Boxplot of P. rapae centroid size (CS) with the mean, standard error, and standard deviation illustrating variations in wing size across geographical populations.

Fig. 6 in A geometric morphometric study of the wing shapes of Pieris rapae (Lepidoptera: Pieridae) from the Qinling Mountains and adjacent regions: An environmental and distance-based consideration

Fig. 6. UPGMA tree of P. rapae forewing and hind wing among different populations, based on Euclidian distances between mean wing shapes. The cluster numbers are population IDs (see Table 1).The groups are divided by Euclidian distances, i.e., the forewing divided by a linkage distance at 0.0027 and the hind wing by a linkage distance at 0.0038.

Fig. 2 in Sexual dimorphism and population differentiation in the Chilean Neotropical moth Macaria mirthae (Lepidoptera, Geometridae): a wing geometric morphometric example

Fig. 2. Benítez et al. (2015), representation of the 13 morphological landmarks identified in the forewings of Macaria mirthae.

Fig. 3 in Sexual dimorphism and population differentiation in the Chilean Neotropical moth Macaria mirthae (Lepidoptera, Geometridae): a wing geometric morphometric example

Fig. 3. PCA analysis of the sexual shape dimorphism of Macaria mirthae: the figure shows the first two orthogonal PC components' axes that represent the shape space dimensions, also a decomposition of shape variation between sexes. *Each point represents a different shape.

Fig. 5 in Sexual dimorphism and population differentiation in the Chilean Neotropical moth Macaria mirthae (Lepidoptera, Geometridae): a wing geometric morphometric example

Fig. 5. Multivariate regression of the wing shape on the wing centroid size of Macaria mirthae. Grey points represent female wings and black points represent male wings.

Fig. 1 in Sexual dimorphism and population differentiation in the Chilean Neotropical moth Macaria mirthae (Lepidoptera, Geometridae): a wing geometric morphometric example

Fig. 1. Graphical scheme of the location of the two Valleys in Atacama Desert in the north of Chile.

Fig. 10 in Wing geometric morphometrics to distinguish and identify Haematobosca flies (Diptera: Muscidae) from Thailand

Fig. 10. Hierarchical agglomerative clustering tree based on shape similarities of test specimens (male as yellow and female as gray) and reference data of Haematobosca sanguinolenta and H. aberrans. Euclidean distances were used for the construction of the tree. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2 in Wing geometric morphometrics to distinguish and identify Haematobosca flies (Diptera: Muscidae) from Thailand

Fig. 2. The topographic map of the Haematobosca fly collection sites in Thailand: Chiang Mai (1), Kanchanaburi (2), and Nakhon Ratchasima (3) (A). The Nzi trap used for fly collection was placed near animal hosts at each collection site (B, C). This map was prepared from the United States Geological Survey (USGS) National Map Viewer available at http://viewer.nationalmap.gov/viewer/, accessed on February 10, 2023.

Fig. 9 in Wing geometric morphometrics to distinguish and identify Haematobosca flies (Diptera: Muscidae) from Thailand

Fig. 9. Factor map of the principal components (PC1, 46% as horizontal axis and PC2, 22% as vertical axis) from wing shape variables of test specimens (male and female) and reference data of Haematobosca sanguinolenta and H. aberrans. Squares represent mean values in each group.

Fig. 8 in Wing geometric morphometrics to distinguish and identify Haematobosca flies (Diptera: Muscidae) from Thailand

Fig. 8. Linear regression between centroid size and the first shape-based principal component (PC) of Haematobosca sanguinolenta (A) and H. aberrans (B). Linear regression prediction is shown by the orange dots. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3. The 10 in Wing geometric morphometrics to distinguish and identify Haematobosca flies (Diptera: Muscidae) from Thailand

Fig. 3. The 10 landmarks on the wing of Haematobosca flies used in the wing geometric morphometric analysis.

Fig. 7 in Wing geometric morphometrics to distinguish and identify Haematobosca flies (Diptera: Muscidae) from Thailand

Fig. 7. Hierarchical agglomerative clustering tree based on shape similarities of each individual for male and female Haematobosca sanguinolenta and H. aberrans. Euclidean distances were used for the construction of the tree.