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20 results for “Hirsutella”
Figure 1 in Toxicity and ovicidal activity of different entomopathogenic fungi, Hirsutella extracts on Tetranychus urticae (Acari: Tetranychidae)
Figure 1. Accumulated mortality of T. urticae females at 24, 48 and 72 h after being fed with mulberry leaf discs treated with different concentrations of crude extract, six species of Hirsutella under residual effect bioassay. For each extract and mite, means followed by the same letter are not significantly different (p = 0.05; Tukey HDS test).
Fig. 4 in Mexican strains of Hirsutella isolated from Diaphorina citri (Hemiptera: Liviidae): Morphologic and molecular characterization
Fig. 4. Production of mucilaginous colonies by Hirsutella citriformis Mexican strains under dark conditions. Mucilaginous colony produced by strain INIFAP- Hir-1 (lef) and colonies without mucilage in strain IB-Hir-1 (right), both afer 5 days of culture under dark conditions.
Fig. 1 in Mexican strains of Hirsutella isolated from Diaphorina citri (Hemiptera: Liviidae): Morphologic and molecular characterization
Fig. 1. Phylogenetic tree constructed with sequences of ITS1-5.8S-ITS2 of 19 Hirsutella species enlisted in the NCBI and 7 Mexican strains isolated from D. citri in Mexico. Percentages from bootstrap analysis that support branches in the tree are shown in the respective nodes. Scale represents the number of substitutions/100 nucleotides.
Fig. 5 in Mexican strains of Hirsutella isolated from Diaphorina citri (Hemiptera: Liviidae): Morphologic and molecular characterization
Fig. 5. Mortality of Diaphorina citri caused by Hirsutella citriformis blastospores. Values followed by the same letter did not differ statistically (Tukey; P = 0.05). Lines in the bars indicate SD.
Fig. 1 in Hirsutella sp. (Hypocreales: Ophiocordycipitaceae) affecting the invasive social wasp Vespula vulgaris (Hymenoptera: Vespidae) in southern Chile
Fig. 1. Vespula vulgaris adult infected with Hirsutella sp. found in southern Chile. A. Mycotized wasp cadaver; B–C. synnema arising from the abdomen of the wasp; D. conidiogenous cells with cylindrical bases and an elongated, narrowed neck; E. conidiogenous cells and conidia. Horizontal scale bars represent 20 µm in C, D, and E.
Fig. 1 in Effect of Mexican Hirsutella citriformis (Hypocreales: Ophiocordycipitaceae) strains on Diaphorina citri (Hemiptera: Liviidae) and the predators Chrysoperla rufilabris (Neuroptera: Chrysopidae) and Hippodamia convergens (Coleoptera: Coccinellidae)
Fig. 1. Overall mean mortality of Diaphorina citri adults caused by conidia of 8 Hirsutella citriformis strains applied by contact (3 separate bioassays) under controlled conditions (26 ± 1 °C, 76 ± 4% RH, 16:8 h L:D photoperiod). Error bars represent the standard error (n = 7).
Fig. 3 in Effect of Mexican Hirsutella citriformis (Hypocreales: Ophiocordycipitaceae) strains on Diaphorina citri (Hemiptera: Liviidae) and the predators Chrysoperla rufilabris (Neuroptera: Chrysopidae) and Hippodamia convergens (Coleoptera: Coccinellidae)
Fig. 3. Mean mortality of Diaphorina citri caused by blastospores of 5 Hirsutella citriformis strains under controlled conditions (26 ± 1 °C, 76 ± 4% RH, 16:8 h L:D photoperiod) during 26 d post inoculation. Different letters indicate significant differences (Tukey's test, α = 0.05). Error bars represent the standard error (n = 7).
Figure 2 in First record of Hirsutella saussurei in the Galápagos Islands and first evidence parasitizing the invasive paper wasp, Polistes versicolor
Figure 2. Phialidae (conidia attached at the apical part of the sterigmata) ofH. saussurei (Cooke) Speare (Ascomycota:Hypocreales) from our sample,photographed using a digital camera attached to a microscope (1000 X) and previously dyed with blue of lactophenol.
Figure 1 in First record of Hirsutella saussurei in the Galápagos Islands and first evidence parasitizing the invasive paper wasp, Polistes versicolor
Figure 1. Synnemata of H. saussurei (Cooke) Speare (Ascomycota:Hypocreales) arising from host (P. versicolor (Olivier) (Hymenoptera: Vespidae)), picture was taken during a sampling at Cerro Luna, in Santa Cruz (Galápagos, Ecuador). It is possible to observe the hyphae of the fungi arising from some parts of the wasp body.
FIGURE 14. Bairdoppilata hirsutella Maddocks, n in Taxonomic applications of the esophageal flapper valve in Bairdoppilata and Glyptobairdia (Bairdiidae, Ostracoda), with comments on anatomy, ontogeny, and geography
FIGURE 14. Bairdoppilata hirsutella Maddocks, n. sp. A, molting juvenile, female A–1, specimen 689J, USNM 139894: posterior region of body with zygum, genital lobes, furca, and postabdominal seta. Scale bar = 50 µm.
FIGURE 11. Bairdoppilata hirsutella Maddocks, n in Taxonomic applications of the esophageal flapper valve in Bairdoppilata and Glyptobairdia (Bairdiidae, Ostracoda), with comments on anatomy, ontogeny, and geography
FIGURE 11. Bairdoppilata hirsutella Maddocks, n. sp. H:L scatter plot for 4 specimens from Eltanin station 25: Holotype specimen 634M (USNM 139891), and paratype specimens 635F (USNM 139892), 636W, and 689J (USNM 139894). Also plotted here are specimen 468F (SUM 121353), which was collected in the Gulf of Mexico and is of uncertain species identity, and the Lectotype RV of Bairdia hirsuta Brady.
FIGURE 13. Bairdoppilata hirsutella Maddocks, n in Taxonomic applications of the esophageal flapper valve in Bairdoppilata and Glyptobairdia (Bairdiidae, Ostracoda), with comments on anatomy, ontogeny, and geography
FIGURE 13. Bairdoppilata hirsutella Maddocks, n. sp. A–D, holotype adult male specimen 634M, USNM 139891: A, dorsal view of zygum, both furcae, and left hemipenis; B, distal element, copulatory tube, and terminal appendages of left hemipenis; C, dorsal view of esophageal valve with ring, collar, belt, plate, and both braces; D, A2 distal claws. E, adult female specimen 635F, USNM 139892: genital lobe. F, molting juvenile specimen 689J, USNM 139894, A–1: detail of antennal claws to show how ramus and claws are withdrawn during molting. Scale bar = 50 µm.
FIGURE 12. Bairdoppilata hirsutella Maddocks, n in Taxonomic applications of the esophageal flapper valve in Bairdoppilata and Glyptobairdia (Bairdiidae, Ostracoda), with comments on anatomy, ontogeny, and geography
FIGURE 12. Bairdoppilata hirsutella Maddocks, n. sp. A–C, molting juvenile specimen 689J, USNM 139894, instar A–1: A, LV interior in reflected light, with narrow infold, broad but weakly calcified inner lamella, and vestibules partly filled with fluid; B, LV interior in reflected light, with AMS, showing striated, hummocky texture of inner chitinous lining, as sensilla and cuticle are being withdrawn from older valve; C, anterior margin of RV interior in reflected light, showing narrow (normal) infold. D–K, holotype adult male specimen 634M, USNM 139891: D–E, LV and RV interiors in reflected light, with broad calcified inner lamella, shallow vestibules separated ventrally, prominent selvage and fringes; F, RV interior, posterodorsal edge with denticles of supplemental dentition; G, LV interior, posterodorsal edge with locules of supplemental dentition beneath dorsal overhang; H–I, RV and LV exteriors in transmitted light, with broad (normal) inner lamellae, fairly deep vestibules, NPC, sensilla, and AMS; J–K, RV and LV exteriors in reflected light, showing smooth surface and sensilla; RV caudal process is damaged. L–M, adult female specimen 635F, USNM 139892: RV and LV exteriors in transmitted light, with AMS and sensilla. Scale bar = 50 µm.
Supplementary material 1 from: Qu J, Zou X, Cao W, Xu Z, Liang Z (2021) Two new species of Hirsutella (Ophiocordycipitaceae, Sordariomycetes) that are parasitic on lepidopteran insects from China. MycoKeys 82: 81-96. https://doi.org/10.3897/mycokeys.82.66927
Tables S1–S3. A total of 71 taxa were selected to represent the morphological and ecological diversity of Hirsutella asexual morphs and Ophiocordyceps
Fig. 2 in Mexican strains of Hirsutella isolated from Diaphorina citri (Hemiptera: Liviidae): Morphologic and molecular characterization
Fig. 2. Phylogenetic tree constructed with sequences of the 28S ribosomal gene of 14 Hirsutella species enlisted in the NCBI and 7 Mexican strains isolated from D. citri in Mexico. Percentages from bootstrap analysis that support branches in the tree are shown in the respective nodes. Scale represents the number of substitutions/100 nucleotides.
Fig. 3 in Mexican strains of Hirsutella isolated from Diaphorina citri (Hemiptera: Liviidae): Morphologic and molecular characterization
Fig. 3. Percentage of mucilaginous colonies developed from fragments of mycelial colonies of 7 Hirsutella Mexican strains afer 5 days under dark conditions. Values followed by the same letter did not differ statistically (Tukey; P = 0.05). Lines in the bars indicate SD.
Figure 1 from: Qu J, Zou X, Cao W, Xu Z, Liang Z (2021) Two new species of Hirsutella (Ophiocordycipitaceae, Sordariomycetes) that are parasitic on lepidopteran insects from China. MycoKeys 82: 81-96. https://doi.org/10.3897/mycokeys.82.66927
Figure 1 Phylogenetic tree of Hirsutella species combined with RPB1, tef1, ITS, 18S rDNA and 28S rDNA datasets, using the maximum likelihood method. Numbers below the branches are bootstrap percentage values, based on 10,000 replicates, ML/BPP.
Figure 3 from: Qu J, Zou X, Cao W, Xu Z, Liang Z (2021) Two new species of Hirsutella (Ophiocordycipitaceae, Sordariomycetes) that are parasitic on lepidopteran insects from China. MycoKeys 82: 81-96. https://doi.org/10.3897/mycokeys.82.66927
Figure 3 Morphological characteristics of Hirsutella kuankuoshuiensisA the insect specimens with single and thin synnemata (HKAS112885) B, C colonial morphology on PDA agar media for 20 d B shows the front of the colony and C shows the back of the colony D–GLM images showing conidiogenous cells and conidia D, E the structure of conidiogenous cells on mycelia F the images of conidiogenous cells on synnemata (optical microscope) H–J conidial morphology (LM) G conidia with mucilage (SEM). Scale bars: 10 mm (A–C); bar of G was shown in the figure; the rest of the bars were 10 μm. LM, light microscopy; PDA, potato dextrose agar; SEM, scanning electron microscopy.
Figure 2 from: Qu J, Zou X, Cao W, Xu Z, Liang Z (2021) Two new species of Hirsutella (Ophiocordycipitaceae, Sordariomycetes) that are parasitic on lepidopteran insects from China. MycoKeys 82: 81-96. https://doi.org/10.3897/mycokeys.82.66927
Figure 2 Morphological characteristics of Hirsutella flavaA the infected insect specimens with a long and single synnemata (HKAS112884) B, C colonial morphology on PDA agar media for 20 d B shows the front of the colony and C shows the back of the colony D–GLM images of the general morphology of conidiogenous cells and conidia H–KSEM images showing conidiogenous cells and conidial structure; Scale bars: 1 cm (A); 5 cm (B, C), 10 μm (D–G); the rest of the bars are shown in the figure. LM, light microscopy; PDA, potato dextrose agar; SEM, scanning electron microscopy.
Study the Impact of Hirsutella Sinensis Nutrient Supplements Has on Improving Muscle Health and Metabolism in Elderly
ClinicalTrials.gov study NCT05284149. IPD Sharing: NO. Countries: 1. Publications: 0.
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