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167 results for “Predatory mites”
Fig. 1 in The Predatory Mites (Phytoseiidae, Parasitiformes) In The Fauna Of Ukraine: A Review With A Key To Species And New Combinations In The Genus Transeius
Fig. 1. Transeius begljarovi (Abbasova, 1970), ♀ (1–7), Ơ (8, 9): 1 — dorsal shield; 2 — ventral body surface; 3 — metapodal plates; 4 — posterior part of peritremal shield; 5 — chelicera; 6 — spermatheca; 7 — fragment of leg IV; 8 — ventrianal shield; 9 — chelicerae with spermatodactil.
Fig. 3 in The Predatory Mites (Phytoseiidae, Parasitiformes) In The Fauna Of Ukraine: A Review With A Key To Species And New Combinations In The Genus Transeius
Fig. 3. Transeius herbarius (Wainstein, 1960), ♀ (1–7), Ơ (8, 9): 1 — dorsal shield; 2 — ventral body surface; 3 — metapodal plates; 4 — posterior part of peritremal shield; 5 — chelicera; 6 — spermatheca; 7 — fragment of leg IV (macrosetae shown only); 8 — ventrianal shield; 9 — chelicerae with spermatodactil.
Fig. 7 in The Predatory Mites (Phytoseiidae, Parasitiformes) In The Fauna Of Ukraine: A Review With A Key To Species And New Combinations In The Genus Transeius
Fig. 7. Transeius montanus (Wainstein, 1962), ♀ (1–7), Ơ (8, 9): 1 — dorsal shield; 2 — ventral body surface; 3 — metapodal plates; 4 — posterior part of peritremal shield; 5 — chelicera; 6 — spermatheca; 7 — fragment of leg IV; 8 — ventrianal shield; 9 — chelicerae with spermatodactil.
Fig. 8 in The Predatory Mites (Phytoseiidae, Parasitiformes) In The Fauna Of Ukraine: A Review With A Key To Species And New Combinations In The Genus Transeius
Fig. 8. Transeius proximus (Кolоdoсhкa, 1991), ♀ (1–9), Amblyseius (Amblyseius) avetianae Arutujan et Ohandjanian, 1972 (10): 1 — dorsal shield; 2 — ventral body surface; 3 — metapodal plates; 4 — caudal part of peritremal shield;5 — chelicera; 6 — spermatheca; 7 — fragment of leg IV; 8 — chelicera; 9, 10 — spermatheca.
Fig. 6 in The Predatory Mites (Phytoseiidae, Parasitiformes) In The Fauna Of Ukraine: A Review With A Key To Species And New Combinations In The Genus Transeius
Fig. 6. Transeius masseei (Nesbitt, 1951), ♀ (1–7), Ơ (8, 9): 1 — dorsal shield; 2 — ventral body surface; 3 — metapodal plates; 4 — posterior part of peritremal shield; 5 — chelicera; 6 — spermatheca; 7 — fragment of leg IV (macrosetae shown only); 8 — ventrianal shield; 9 — chelicerae with spermatodactil.
Fig. 9 in The Predatory Mites (Phytoseiidae, Parasitiformes) In The Fauna Of Ukraine: A Review With A Key To Species And New Combinations In The Genus Transeius
Fig. 9. Transeius volgini (Wainstein et Beglyarov, 1971), ♀ (1–8), Ơ (9, 10): 1 — dorsal shield; 2 — backward curved ends of peritremes; 3 — posterior part of ventral body surface; 4 — metapodal plates; 5 — posterior part of peritremal shield; 6 — chelicera; 7 — spermatheca; 8 — fragment of leg IV; 9 — ventrianal shield; 10 — chelicerae with spermatodactil.
Unexpected effects of local management and landscape composition on predatory mites and their food resources in vineyards
<p>This research was funded by the project SECBIVIT.</p> <p>Dataset of the results in the Articel: Unexpected effects of local management and landscape composition on predatory mites and their food resources in vineyards.</p> <p>For further information also see: </p> <ul> <li>Sampled grape varieties: http://doi.org/10.5281/zenodo.4562219 </li> <li>https://www.secbivit.boku.ac.at/</li> </ul>
Figure 12 in Additional contributions to the knowledge of Philippine predatory mites mainly of the subfamilies Cunaxinae and Cunaxoidinae (Acari: Prostigmata: Cunaxidae)
Figure 12 Scutopalus clavatus (Shiba), female idiosoma: a – dorsum; b – venter. Scale bar 100 µm.
Figure 7 in Additional contributions to the knowledge of Philippine predatory mites mainly of the subfamilies Cunaxinae and Cunaxoidinae (Acari: Prostigmata: Cunaxidae)
Figure 7 Lupaeus longisetus (Corpuz-Raros), female: a – gnathosoma; b – chelicera. Scale bar 50 µm.
Figure 2 Cunaxa minidiscondyla n in Additional contributions to the knowledge of Philippine predatory mites mainly of the subfamilies Cunaxinae and Cunaxoidinae (Acari: Prostigmata: Cunaxidae)
Figure 2 Cunaxa minidiscondyla n. sp., female idiosoma: a – dorsum; b – venter. Scale bar 100 µm.
Figure 1 Cunaxa minidiscondyla n in Additional contributions to the knowledge of Philippine predatory mites mainly of the subfamilies Cunaxinae and Cunaxoidinae (Acari: Prostigmata: Cunaxidae)
Figure 1 Cunaxa minidiscondyla n. sp., female: a – subcapitulum; b – palp; c – chelicera. Scale bar
Figure 2 in Functional and numerical responses of the predatory mite Amblyseius aerialis (Acari: Phytoseiidae) toAceria guerreronis (Acari: Eriophyidae)
Figure 2 Mean number of eggs laid byAmblyeius aerialis females provided with different densities
Figure 3 in Functional and numerical responses of the predatory mite Amblyseius aerialis (Acari: Phytoseiidae) toAceria guerreronis (Acari: Eriophyidae)
Figure 3 Average oviposition rates (eggs/female ± SE) byAmbyseius aerialis females given different
Figure 3 in Quality control of the predatory mite Euseius scutalis (Acari: Phytoseiidae) againstTetranychus turkestani (Acari: Tetranychidae) over 30 generations of rearing on cattail pollen
Figure 3 Offspring sex ratio of females of Euseius scutalis fedTetranychus turkestani before (G0)
Figure 1 in Quality control of the predatory mite Euseius scutalis (Acari: Phytoseiidae) againstTetranychus turkestani (Acari: Tetranychidae) over 30 generations of rearing on cattail pollen
Figure 1 he age-stage survival rate (sxj) of Euseius scutalis fedTetranychus turkestani before (G0)
Table 1 in Predation and oviposition potential of Brazilian populations of the predatory mite Amblyseius tamatavensis (Acari: Phytoseiidae) on eggs of Bemisia tabaci (Insecta: Hemiptera)
<p><b>Table 1</b> Sites and plants where the populations of <i>Amblyseius tamatavensis</i> were collected in Brazil (May 2015 to May 2016).</p><table><tbody><tr><th>Populations</th><th><b>Substrate</b></th></tr></tbody><tbody><tr><th>1.Olho d’Água das Flores (Alagoas)</th><td><i>Ipomoea pes-caprae</i> (Convolvulaceae)</td></tr><tr><th>2.Jataí (Goiás)</th><td>Several plants</td></tr><tr><th>3.Nova Crixás (Goiás)</th><td>Several plants</td></tr><tr><th>4.Bom Repouso (Minas Gerais)</th><td>Several plants</td></tr><tr><th>5.Ituiutaba (Minas Gerais)</th><td>Several plants</td></tr><tr><th>6.Senador Amaral (Minas Gerais)</th><td>Several plants</td></tr><tr><th>7.Campinas (São Paulo)</th><td><i>Psidium guajava</i> (Myrtaceae)</td></tr><tr><th>8.Cananéia (São Paulo)</th><td><i>Persea americana</i> (Lauraceae)</td></tr><tr><th>9.Mogi Guaçu (São Paulo)</th><td><i>Citrus</i> sp. (Rutaceae)</td></tr><tr><th>10.Piracicaba, ESALQ (São Paulo)</th><td><i>Gossypium</i> sp. (Malvaceae)</td></tr><tr><th>11.Piracicaba, Areão (São Paulo)</th><td><i>Rosa</i> sp. (Rosaceae)</td></tr><tr><th>12.Saltinho (São Paulo)</th><td><i>Cocos nucifera</i> (Arecaceae)</td></tr><tr><th>13.Santa Maria da Serra (São Paulo)</th><td>Several plants</td></tr><tr><th>14. Laboratory</th><td><i>Capsicum annuum</i> (Solanaceae)</td></tr></tbody></table>
Table 3 in Predation and oviposition potential of Brazilian populations of the predatory mite Amblyseius tamatavensis (Acari: Phytoseiidae) on eggs of Bemisia tabaci (Insecta: Hemiptera)
<p><b>Table 3</b> Daily means (± standard error of the mean) of eggs of <i>Bemisia tabaci</i> killed and eggs laid by adult female of populations of <i>Amblyseius tamatavensis</i> collected in different Brazilian municipalities.</p><table><tbody><tr><th><b>Collection sites</b></th><th><b>Predation</b></th><th><b>Oviposition</b></th></tr></tbody><tbody><tr><th>Olho d’água das Flores</th><td>7.9 ± 0.7 a</td><td>1.2 ± 0.2 a</td></tr><tr><th>Laboratório</th><td>7.0 ± 0.4 b</td><td>1.1 ± 0.3 ab</td></tr><tr><th>Jataí</th><td>6.5 ± 0.4 c</td><td>0.8 ± 0.1 c</td></tr><tr><th>Saltinho</th><td>6.5 ± 0.3 c</td><td>1.0 ± 0.1 b</td></tr><tr><th>Mogi-Guaçu</th><td>6.5 ± 0.3 c</td><td>0.8 ± 0.0 c</td></tr><tr><th>Piracicaba - Fazenda Areão</th><td>6.5 ± 0.2 c</td><td>1.0 ± 0.2 b</td></tr><tr><th>Senador Amaral</th><td>6.5 ± 0.1 c</td><td>0.9 ± 0.3 bc</td></tr><tr><th>Bom Repouso</th><td>6.3 ± 0.3 cd</td><td>0.9 ± 0.2 bc</td></tr><tr><th>Ituiutaba</th><td>6.3 ± 0.2 cd</td><td>0.8 ± 0.1 c</td></tr><tr><th>Campinas</th><td>6.3 ± 0.2 cd</td><td>1.0 ± 0.1 b</td></tr><tr><th>Cananéia</th><td>6.3 ± 0.1 cd</td><td>0.9 ± 0.2 bc</td></tr><tr><th>Santa Maria da Serra</th><td>6.1 ± 0.4 d</td><td>0.8 ± 0.1 c</td></tr><tr><th>Piracicaba - ESALQ</th><td>6.0 ± 0.5 d</td><td>0.9 ± 0.1 bc</td></tr><tr><th>Nova Crixás</th><td>5.0 ± 0.3 e</td><td>0.7 ± 0.2 c</td></tr></tbody></table><p>For each column, rates followed by the same letter are not statistically different (Kruskal-Wallis ANOVA; Dunn´s test).</p>
Figure 2 in Evaluation of prey stage preference of the predatory miteNeoseiulus longispinosus (Evans) on the spider mite pest Tetranychus neocaledonicus (André) (Acari: Phytoseiidae, Tetranychidae)
Figure 2 Mean consumption rate (%) of nymphs of Neoseiulus longispinosus on different life stages
Figure 1 in Evaluation of prey stage preference of the predatory miteNeoseiulus longispinosus (Evans) on the spider mite pest Tetranychus neocaledonicus (André) (Acari: Phytoseiidae, Tetranychidae)
Figure 1 Mean consumption rate (%) of adults of Neoseiulus longispinosus on different life stages
Figure 4 in Suitability of different pollen grains and Tetranychus urticae as food for the predatory mite, Amblyseius swirskii (Acari: Phytoseiidae)
Figure 4. Exine patterns of four plant pollens prepared using a Scanning Electron Microscopy (SEM).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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