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167 results for “Predatory mites”
FIGURES 21–25 in Predatory mites from crops and pastures in South Africa: potential natural enemies of redlegged earth mite Halotydeus destructor (Acari: Penthaleidae)
FIGURES 21–25. Macrocheles propinquus sp. nov., female. 21. dorsal idiosoma; 22. ventral idiosoma; 23 epistome; 24. chelicera; 25. hypostome. Scale bar = 100 µm for 21, 22, 50 µm for 23, 24, 25.
FIGURES 43–47 in Predatory mites from crops and pastures in South Africa: potential natural enemies of redlegged earth mite Halotydeus destructor (Acari: Penthaleidae)
FIGURES 43–47. Pachylaelaps meganalis sp. nov., female. 43. dorsal idiosoma; 44. ventral idiosoma; 45. epistome; 46. chelicera; 47. hypostome. Scale bar = 100 µm for 43, 44, 80 µm for 45, 46, 47.
FIGURES 37–42 in Predatory mites from crops and pastures in South Africa: potential natural enemies of redlegged earth mite Halotydeus destructor (Acari: Penthaleidae)
FIGURES 37–42. Gamasiphoides rykei sp. nov., female. 37. dorsal idiosoma; 38. ventral idiosoma; 39. epistome; 40. chelicera; 41. hypostome; 42. palp genu. Scale bar = 100 µm for 37, 38, 50 µm for 40, 41. 42, 30 µm for 39.
FIGURES 10–15. 10 in Predatory mites from crops and pastures in South Africa: potential natural enemies of redlegged earth mite Halotydeus destructor (Acari: Penthaleidae)
FIGURES 10–15. 10. Hypoaspis calcarata sp. nov., female. 10, dorsal idiosoma. 11, ventral idiosoma. 12, hypostome. 13, chelicera. 14, epistome. 15, femur, genu and tibia I. Scale bar 100 µm for 10, 11, 50 µm for 12, 13, 14, 15.
FIGURES 34–36 in Predatory mites from crops and pastures in South Africa: potential natural enemies of redlegged earth mite Halotydeus destructor (Acari: Penthaleidae)
FIGURES 34–36. Gamasiphoides lootsi sp. nov., male. 34. sternitigenital shield; 35. chelicera; 36. femur, genu, and tibia of leg II. Scale bar = 100 µm for 34, 80 µm for 35, 36.
FIGURES 2–7 in Predatory mites from crops and pastures in South Africa: potential natural enemies of redlegged earth mite Halotydeus destructor (Acari: Penthaleidae)
FIGURES 2–7. Bdellodes edentata, sp. nov., female. 2, dorsal idiosoma. 3, ventral idiosoma and coxae. 4, hypostome. 5, palp. 6, chelicera. 7, tibia and tarsus I, dorsal aspect. Scale bar = 100 µm.
FIGURES 16–18 in A new species of predatory Scolothrips (Thysanoptera, Thripidae) feeding on Raoiella mites (Tenuipalpidae) in Australia
FIGURES 16–18. Scolothrips asura female. (16) Antenna; (17) Pro, meso and metanota; (18) Tergites I–III.
FIGURES 8–15 in A new species of predatory Scolothrips (Thysanoptera, Thripidae) feeding on Raoiella mites (Tenuipalpidae) in Australia
FIGURES 8–15. Scolothrips ochoa sp. n. female illuminated with Differential Interference Contrast (8) Head & pronotum; (9) Ventral surface of head; (10) Antenna; (11) Forewing dark area; (12) Tergites VIII–X; (13) Thoracic sternites; (14) Meso and metanota; (15) Tergites I–III.
FIGURES 5–7 in A new species of predatory Scolothrips (Thysanoptera, Thripidae) feeding on Raoiella mites (Tenuipalpidae) in Australia
FIGURES 5–7. Scolothrips ochoa sp. n. (5) Larva feeding on larval Raoiella; (6) Pupa with Raoiella eggs and nymphal skins; (7) Four images from cine film of pupa and emerging adult (note white cast cuticle: (a) Start of filming; (b) at 6 minutes; (c) at 11 minutes; (d) at 94 minutes).
FIGURES 1–4 in A new species of predatory Scolothrips (Thysanoptera, Thripidae) feeding on Raoiella mites (Tenuipalpidae) in Australia
FIGURES 1–4. Scolothrips ochoa sp. n. (1) Host tree, Lophostemon suaveolens; (2) Adult female feeding on Raoiella egg; (3) Slide mounted adult female; (4) Female head and antennae.
FIGURES 14–19 in Taxonomic notes on the predatory mite genus Proparholaspulus Ishikawa, 1980 and the first description of the male of Proparholaspulus ishikawai Liang & Hu 1993 (Acari: Parholaspididae)
FIGURES 14–19. Proparholaspulus ishikawai Liang & Hu, 1993, female. 14. Median projection of epistome; 15. Lateral projection of epistome; 16. Sternal shield; 17. Geniti-ventrianal shield; 18. Hypostome; 19. Tarsus II. Scale bar 14, 15 = 10μm; 16–19 = 50μm.
FIGURES 12–13 in Taxonomic notes on the predatory mite genus Proparholaspulus Ishikawa, 1980 and the first description of the male of Proparholaspulus ishikawai Liang & Hu 1993 (Acari: Parholaspididae)
FIGURES 12–13. Proparholaspulus ishikawai Liang & Hu, 1993, female. 12. Dorsum; 13. Venter. Scale bar 12, 13 = 1000μm.
FIGURES 1–2 in Taxonomic notes on the predatory mite genus Proparholaspulus Ishikawa, 1980 and the first description of the male of Proparholaspulus ishikawai Liang & Hu 1993 (Acari: Parholaspididae)
FIGURES 1–2. Proparholaspulus ishikawai Liang & Hu, 1993, male. 1. Dorsum; 2. Venter. Scale bar 1, 2 = 100μm.
FIGURES 3–7 in Taxonomic notes on the predatory mite genus Proparholaspulus Ishikawa, 1980 and the first description of the male of Proparholaspulus ishikawai Liang & Hu 1993 (Acari: Parholaspididae)
FIGURES 3–7. Proparholaspulus ishikawai Liang & Hu, 1993, male. 3. Tritosternum; 4. Gnathosoma; 5. Palp; 6. Chelicera; 7. Epistome; Scale bar 3–7 = 50μm.
FIGURES 8–11 in Taxonomic notes on the predatory mite genus Proparholaspulus Ishikawa, 1980 and the first description of the male of Proparholaspulus ishikawai Liang & Hu 1993 (Acari: Parholaspididae)
FIGURES 8–11. Proparholaspulus ishikawai Liang & Hu, 1993, male. 8. Leg I; 9. Leg II; 10. Leg III; 11. Leg IV. Scale bar 8–11 = 100μm.
Data from: A tiny cuckoo: risk-dependent interspecific brood parasitism in a predatory mite
<p><span>Many animal species protect their eggs against predators while others do not. When these species share the same habitat, the latter species may profit by adding their eggs to those of the protecting species. We show that one tiny predatory mite species protects its own eggs only to a limited extent, and instead adds them to those of another predatory mite species that does guard its eggs, resulting in reduced egg predation. This cuckoo behaviour comes with a cost, and therefore only occurs when egg predators are present. Furthermore, the parasites only add eggs to those of the guarding host species, not to those of another mite species that does not guard its eggs. To the best of our knowledge, this is the first study to show that facultative brood parasitism is more effective than brood care, in increasing offspring survival in the presence of egg predators.</span></p>
Northward range expansion of rooting ungulates decreases detritivore and predatory mite abundances in boreal forests
<p>The last decades wild boar populations have expanded northwards, colonizing boreal forests. The soil disturbances caused by wild boar rooting may have an impact on soil organisms that play a key role in organic matter turnover. However, the impact of wild boar colonisation on boreal forest ecosystems and soil organisms remains largely unknown. We investigated the effect of natural and simulated rooting on decomposer and predatory soil mites (total, adult and juvenile abundances; and proportion of adult-juvenile). Our simulated rooting experiment aimed to disentangle the effects of a) bioturbation due to soil mixing and b) removing organic material (wild boar food resources) on soil mites. Our results showed a decline in the abundance of adult soil mites in response to both natural and artificial rooting, while juvenile abundance and the relative proportion of adult-juvenile were not affected. The expansion of wild boar northwards and into new habitats has negative effects on soil decomposer abundances in boreal forests which may cascade through the soil food web ultimately affecting ecosystem processes. Our study also suggests that a combined use of natural and controlled experimental approaches is the way forward to reveal any subtle interaction between aboveground-belowground organisms and the ecosystem functions they drive.</p>
FIGURE 2 in Phytophagous and predatory mites on olive trees in Tunisia. Catalogue, description of one new species and key for identification (Acari, Eriophyidae, Tetranychidae, Tenuipalpidae and Phytoseiidae)
FIGURE 2: Ventral shields of the female of Typhlodromus (Anthoseius) mathieui n. sp.
FIGURE 1 in Phytophagous and predatory mites on olive trees in Tunisia. Catalogue, description of one new species and key for identification (Acari, Eriophyidae, Tetranychidae, Tenuipalpidae and Phytoseiidae)
FIGURE 1: Dorsal shield and peritreme of the female of Typhlodromus (Anthoseius) mathieui n. sp.
FIGURE 4 in Sustainable weed management and predatory mite (Acari: Phytoseiidae) dynamics in Tunisian citrus orchards
FIGURE 4: Mean Phytoseiidae densities (a) per citrus leaf, (b) per weed quadrat and (c) per trap for the two weeding modalities in three citrus species orchards of the experimental 2.
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