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87 results for “Bombyx”
Fig. 4 in Standard method for detecting Bombyx mori nucleopolyhedrovirus disease-resistant silkworm varieties
Fig. 4. IIM for placing silkworms on mulberry leaves. (A) One larva was placed on each leaf. (B) The larva eating the leaf. (C) The leaf after being eaten by the silkworm.
Fig. 3 in Standard method for detecting Bombyx mori nucleopolyhedrovirus disease-resistant silkworm varieties
Fig. 3. GIM for placing silkworms on mulberry leaves. (A) The leaves were arranged in the box after smearing them with BmNPV, and then they were air dried. (B) Five larvae were placed on each leaf. (C) The leaves after being eaten by the silkworms.
Figure 5 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 5. TEM micrograph of chitosan nanoparticles prepared by ionic gelation method. Table 3. Antimicrobial activity of silver nanoparticles (µl) with different concentrations against fungal and bacterial isolates.
Figure 1 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 1. Mean weight of healthy and infected fourth and fifth instar larvae of B. mori. Isolation and identification of bacterial isolates: Total of 7 bacterial were successfully isolated from the outer surface and the inner bоdy of silkworm larvae.
Figure 4 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 4. Transmissiоn electron microscоpy micrоgraph of silver nanoparticles.
Figure 3 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 3. Final dispersion formed after reduction (A) silver and (B) chitosan.
Mechanism of Ca2+ in regulating pupation defects of Bombyx mori after exposure to chlorantraniliprole
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Knockdown of BmorCPR67 gene disrupts prepupal–pupal transition of silkworm Bombyx mori by thinning the endocuticle
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Data from: Role of Atg3, Atg5, and Atg12 in the crosstalk between apoptosis and autophagy in the posterior silk gland of Bombyx mori
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FIGURE 7. Spiophanes uschakowi Zachs, 1933 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 7. Spiophanes uschakowi Zachs, 1933: A. Anterior end, dorsal view. B. Chaetiger 5–12, lateral view; arrow indicates simple vertical opening of glandular organ in chaetiger 11. C. Neuropodial hooks with reduced hood from chaetiger 19. — All Syntype, RAS 1/25826. Scale: A, B 0.5 mm; C 10 µm.
FIGURE 8 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 8. First presence of neuropodial hooks in relation to body width on chaetiger 4 in both Spiophanes bombyx and S. norrisi sp. nov.
FIGURE 5 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 5. Spiophanes norrisi sp. nov.: A. Anterior end, dorsal view; methyl green stained nuchal and dorsal ciliated organs. B. Anterior end, lateral view; methyl green stained openings of glandular organs on chaetigers 5, 7, and 8; arrow indicates simple vertical opening of glandular organ in chaetiger 14. C–F. Parapodium from chaetiger 2, 5, 11, and 19, all anterior view. G. Neuropodial hooks with reduced hood from chaetiger 19. H. Neuropodial chaeta from chaetiger 5. I. Sabre chaeta from chaetiger 11. K. Neuropodial chaeta from chaetiger 2. — B = LACM–AHF V. 1962–50 (Paratype); all others LACM–AHF V5102. Scale: A, B 0.5 mm, C–F 0.1 mm. G–K 5 µm.
FIGURE 2 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 2. Spiophanes bombyx (Claparède, 1870): A. Anterior end, dorsal view. B. Chaetigers 9–15 with dorsal ciliated organs and dorsal ciliated crests, dorsal view. — Specimens from the North Sea, German Bight, depth 24 m, leg. K. Meißner, Jul 2008. Scale: in µm.
FIGURE 10 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 10. Phylogenetic relationships among five Spiophanes species based on partial mitochondrial and nuclear sequences. A. Maximum–likelihood bootstrap consensus tree (1000 replicates) based on COI haplotypes. Numbers above branches are likelihood bootstrap values; numbers below branches are Bayesian posterior probabilities and parsimony consensus percentages. Trees are rooted using sequences of Prionospio as outgroup (P. steenstrupi EU835668; Prionospio sp.1 EU835667). B. Maximum–parsimony bootstrap consensus tree (1000 replicates) based on 18S haplotypes. Numbers above branches are parsimony bootstrap values; numbers below branches are Bayesian posterior probabilities and likelihood bootstrap percentages. Trees are rooted using sequences of Prionospio as outgroup (P. ehlersi EU340095; P. dubia EU418859).
FIGURE 3 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 3. Spiophanes bombyx (Claparède, 1870): Chaetiger 10–18, dorsal view, methyl green stained nuchal organs. — Specimen from Turkey, Iskenderum Bay, sublittoral, leg. E. Dagli, Sep 2005. Scale: 0.5 mm.
FIGURE 4 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 4. Spiophanes bombyx (Claparède, 1870): A. Chaetigers 4–9 with openings of glandular organs on chaetigers 5, 7, 8, 9, lateral view. B. Neuropodial hooks from chaetiger 16, dorsal apical view. C. Chaetigers 9–11, lateral view. D. Posterior end with stout curved notochaeta, dorsal view. — A, B, D specimens from the North Sea, German Bight, depth 24 m, leg. K. Meißner, Jul 2008; C specimen from the Gulf of Naples, depth 20 m, leg. P. Lanera, March 2005. Scale: in µm.
FIGURE 9 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 9. Number of neuropodial hooks in relation to body width on chaetiger 4 in both Spiophanes bombyx and S. norrisi sp. nov.
X-ray diffraction images of juvenile hormone diol kinase from the silk worm Bombyx mori
<p>X-ray diffraction images of juvenile hormone diol kinase (JHDK) from the silk worm Bombyx mori</p>
FIGURE 31 in Systematic position of Bombyx incomposita (Lepidoptera: Bombycidae), with notes on its immature biology and hostplant association
FIGURE 31. Phylogenetic tree of the Bombycinae for 6 genera (11 species) constructed using maximum likelihood and Bayesian inference for the combined 6 genes (COI, CAD, EF-1α, GAPDH, RpS5 and wgl). Bombyx incomposita is sister to B. huttoni. Support values are indicated by bootstrap and Bayesian posterior probability on respective branches. Branch lengths are proportional to inferred substitution rate.
FIGURES 24–30 in Systematic position of Bombyx incomposita (Lepidoptera: Bombycidae), with notes on its immature biology and hostplant association
FIGURES 24–30. Genitalia and wing venation of Bombyx incomposita: 24, male genitalia; 25, phallus (posterior on the right, anterior on the left); 26, tergum VIII; 27, sternum VIII; 28, female genitalia; 29, forewing; 30, hindwing. Scale bars = 2 mm and 10 mm (Figs. 29–30).
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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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