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62 results for “body form”
FIGURE 5 in Two species of nivicolous myxomycetes that formed fruiting bodies during three spring seasons in the lowlands of the Eastern Ukraine
FIGURE 5. Climate conditions in the study area during 2016–2019. Gray line indicates air temperature, grey area represents the thickness of snow cover (days with snow cover>30 cm are above the horizontal black line), and red lines correspond to the beginning/end dates, when myxomycetes were collected.
FIGURE 4. Lamproderma aff. pulchellum Meyl. A–D. Sporocarps. E, F. Capillitium. G. Peridium and spores. H, I in Two species of nivicolous myxomycetes that formed fruiting bodies during three spring seasons in the lowlands of the Eastern Ukraine
FIGURE 4. Lamproderma aff. pulchellum Meyl. A–D. Sporocarps. E, F. Capillitium. G. Peridium and spores. H, I. Spores.
FIGURE 3. Lamproderma pseudomaculatum Mar. Mey. et Poulain. A–D. Sporocarps. E, F. Capillitium. G in Two species of nivicolous myxomycetes that formed fruiting bodies during three spring seasons in the lowlands of the Eastern Ukraine
FIGURE 3. Lamproderma pseudomaculatum Mar. Mey. et Poulain. A–D. Sporocarps. E, F. Capillitium. G. Peridium (arrowheads indicate maculae). H, I. Spores.
FIGURE 2 in Two species of nivicolous myxomycetes that formed fruiting bodies during three spring seasons in the lowlands of the Eastern Ukraine
FIGURE 2. General appearance of collection sites at the time when nivicolous myxomycetes form fruiting bodies. A. National Park Homilsha forest. B, C. Kharkiv Forest-Park. D. Typical abundant fruiting of Lamproderma pseudomaculatum in Kharkiv Forest-Park.
FIGURE 1. Collection sites. 1. Kharkiv Forest-Park. 2. National Nature Park Homilsha Forest. 3 in Two species of nivicolous myxomycetes that formed fruiting bodies during three spring seasons in the lowlands of the Eastern Ukraine
FIGURE 1. Collection sites. 1. Kharkiv Forest-Park. 2. National Nature Park Homilsha Forest. 3. National Nature Park Slobozhanskyi.
Data from: How predation shaped fish: the impact of fin spines on body form evolution across teleosts
It is well known that predators can induce morphological changes in some fish: individuals exposed to predation cues increase body depth and the length of spines. We hypothesize that these structures may evolve synergistically, as together, these traits will further enlarge the body dimensions of the fish that gape-limited predators must overcome. We therefore expect that the orientation of the spines will predict which body dimension increases in the presence of predators. Using phylogenetic comparative methods, we tested this prediction on the macroevolutionary scale across 347 teleost families, which display considerable variation in fin spines, body depth and width. Consistent with our predictions, we demonstrate that fin spines on the vertical plane (dorsal and anal fins) are associated with a deeper-bodied optimum. Lineages with spines on the horizontal plane (pectoral fins) are associated with a wider-bodied optimum. Optimal body dimensions across lineages without spines paralleling the body dimension match the allometric expectation. Additionally, lineages with longer spines have deeper and wider body dimensions. This evolutionary relationship between fin spines and body dimensions across teleosts reveals functional synergy between these two traits and a potential macroevolutionary signature of predation on the evolutionary dynamics of body shape.
Figure 19 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 19. Haplochthonius simplex. (A) Anal region of larva; (B) anogenital region of tritonymph. Note: explanation of labels in text.
Figure 15 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 15. Sphaerochthonius splendidus, tritonymph, dorsal aspect. Note: explanation of labels in text.
Figure 13 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 13. Sphaerochthonius splendidus. (A) Anal region of larva; (B) Anogenital region of protonymph. Note: explanation of labels in text.
Figure 14 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 14. Sphaerochthonius splendidus, anogenital region. (A) Deutonymph; (B) Tritonymph. Note: explanation of labels in text.
Figure 11 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 11. Sphaerochthonius splendidus, adult, anogenital region. Note: explanation of labels in text.
Figure 6 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 6. Cosmochthonius ponticus, anogenital region. (A) Deutonymph; (B) Tritonymph. Note: explanation of labels in text.
Figure 5 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 5. Cosmochthonius ponticus, (A) Anal region of larva; (B) anogenital region of protonymph. Note: explanation of labels in text.
Figure 9. Tibia and tarsus I in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 9. Tibia and tarsus I of tritonymphs. (A) Cosmochthonius ponticus, antiaxial aspect; (B) C. ponticus, region of solenidion w; (C) Sphaerochthonius splendidus, antiaxial aspect; (D) S. splendidus, region of solenidion w; (E) S. splendidus, famulus ∈ covered by cerotegument: (F) Haplochthonius simplex, antiaxial aspect; (G) H. simplex, region of solenidion w. Notes: pairs of setae in parentheses; some setae are not illustrated; explanation of labels in text.
Figure 8 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 8. Lateral aspect of tritonymphs. (A) Cosmochthonius ponticus; (B) Sphaerochthonius splendidus. Note: explanation of labels in text.
Figure 7 in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 7. Cosmochthonius ponticus, tritonymph. (A) Dorsal aspect; (B) Fragment of rostrum. Note: explanation of labels in text.
Figure 3. Tibia and tarsus I in Differentiation of body form of Protoplophoroidea (Acari: Oribatida) in the light of ontogeny of three species
Figure 3. Tibia and tarsus I of adults, antiaxial aspect. (A) Cosmochthonius ponticus; (B) Sphaerochthonius splendidus; (C) Haplochthonius simplex. Notes: pairs of setae in parentheses; some setae are not illustrated; explanation of labels in text.
A Trial to Learn How a New Liquid Form of BAY1817080 is Tolerated and Taken up by the Body of Healthy Male Participants (Part A). By Labeling BAY1817080 With a Radioactive Substance (Carbon 14) Resear
ClinicalTrials.gov study NCT04487431. IPD Sharing: NO. Countries: 1. Publications: 1.
Body Responses to Bean Physical Form and "Beano"
ClinicalTrials.gov study NCT02110511. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Data from: Admixture mapping of male nuptial color and body shape in a recently formed hybrid population of threespine stickleback
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