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85 results for “Telenomus”
Figs. 5–10 in Telenomus alecto (Crawford) (Hymenoptera: Scelionidae), parasitoid of Diatraea magnifactella Dyar (Lepidoptera: Crambidae) from Jalisco, Mexico: a study based on morphological and molecular evidence
Figs. 5–10. Telenomus alecto, female: (5) FSCA 00091198, mesosoma, dorsal view; (6) FSCA 00091198, mesosoma, lateral view; (7) FSCA 00091198, mesosoma, posterolateral view; (8) FSCA 00091198,mesosoma, ventrolateral view; (9) FSCA 00091197, T1–T2, anterolateral view; (10) FSCA 00091198, metasoma, dorsal view.
Figs. 2–4 in Telenomus alecto (Crawford) (Hymenoptera: Scelionidae), parasitoid of Diatraea magnifactella Dyar (Lepidoptera: Crambidae) from Jalisco, Mexico: a study based on morphological and molecular evidence
Figs. 2–4. Telenomus alecto, female: (2) FSCA 00091145, head, mesosoma, metasoma, dorsal view; (3) FSCA 00091497, head, anterior view; (4) FSCA 00091497, mouthparts, anteroventral view.
Fig. 1 in Biology of Telenomus pachycoris (Hymenoptera: Scelionidae), a parasitoid of eggs of Pachycoris torridus (Hemiptera: Scutelleridae): the effects of egg age, exposure time, and temperature
Fig. 1. Number of generations of Telenomus pachycoris reared in Pachycoris torridus eggs at different constant temperatures with 70 ± 10% RH and a photoperiod of 12:12 h L:D.
Figure 1 in Toxicity of insecticides to the egg parasitoids Telenomus podisi and Trissolcus teretis (Hymenoptera: Scelionidae)
Figure 1 Bioassay setup. Potter Spray Tower (A), experimental cage (B), Duran tube with adult parasitoids inside covered with aluminum foil used to introduce the wasps into the experimental cage (C), glass plate being sprayed with the Potter Spray Tower before the setup of the experimental cage (D), adult cages mounted with the Duran tube connected (E), experimental cages setup with circulating air flow allowing the elimination of possible toxic gases (F).
Fig. 1 in Telenomus podisi parasitism on Dichelops melacanthus and Podisus nigrispinus eggs at different temperatures
Fig. 1. Distribution of lifetime parasitism of Telenomus podisi Ashmead (Hymenoptera: Scelionidae) in Dichelops melacanthus eggs (Dallas) (Hemiptera: Pentatomidae) at different temperatures. (A) 15 °C, (B) 20 °C, (C) 25 °C, (D) 30 °C at 80 ± 10% RH and a 14:10 h (L:D) photoperiod. Arrows indicate parasitism of 80%.
Telenomus cultratus Mayr, lectotype female, NHMW-HYM#0005385
<p><em>Telenomus cultratus </em>Mayr, 1879: 699, 701, 703</p> <p><em>Aphanurus cultratus</em> (Mayr, 1879) </p> <p><em>Microphanurus cultratus </em>(Mayr, 1879) </p> <p><em>Asolcus cultratus</em> (Mayr, 1879)</p> <p><em>Trissolcus cultratus</em> (Mayr, 1879)</p> <p>This specimen has also been referred to by the following CUID: NHMW 0008A.</p>
Telenomus simoni Mayr, lectotype female, NHMW-HYM#0006879
<p><em>Telenomus simoni</em> Mayr, 1879: 699, 705 (Talamas et al. 2017)</p> <p><em>Telenomus simonii </em>Mayr, 1879</p> <p><em>Trissolcus simoni</em> (Mayr, 1879)</p> <p>This specimen has also been referred to by the following CUID: NHMW 0004.</p>
Telenomus umbripennis Mayr, paralectotype female, NHMW-HYM#0006900
<p><em>Telenomus umbripennis</em> Mayr, 1879: 701, 712</p> <p>Paralectotype and host caterpillar (reared from same group of eggs on oak leaf).</p> <p>Lectotype is nearly destroyed (only mesosoma remains).</p>
Learning can be detrimental for a parasitic wasp: R scripts and Telenomus podisi data
<p>Animals have evolved the capacity to learn, and the conventional view is that learning allows individuals to improve foraging decisions. We describe a first case of maladaptive learning where a parasitoid learns to associate chemical cues from an unsuitable host, thereby re-enforcing a reproductive cul-de-sac (evolutionary trap). <i>Telenomus podisi</i> parasitizes eggs of the exotic stink bug <i>Halyomorpha halys</i> at the same rate as eggs of its coevolved host, <i>Podisus maculiventris</i>, but the parasitoid cannot complete its development in the exotic species. We hypothesized that <i>T. podisi </i>learns to exploit cues from this non-coevolved species, thereby increasing unsuccessful parasitism rates. We conducted bioassays to compare the responses of naïve <i>vs</i>. experienced parasitoids on chemical footprints left by one of the two host species. Both naïve and experienced females showed a higher response to footprints of <i>P. maculiventris</i> than of <i>H. halys</i>. Furthermore, parasitoids that gained an experience on <i>H. halys</i> significantly increased their residence time within the arena and the frequency of re-encounter with the area contaminated by chemical cues. Maladaptive learning in the <i>T. podisi</i> - <i>H. halys</i> association is expected to further decrease parasitoid reproductive success and have consequences for population dynamics of sympatric native and exotic host species.</p>
Telenomus alsophilae, FSCA 00061221
<p><em>Telenomus alsophilae</em> Viereck</p> <p>female, FSCA 00061221</p> <p>USA: MA: AXK: Almanac Pond, 41.28356566N, -70.00078497E, ex. eggs of <em><span>Alsophila pometaria</span></em><span> (Lepidoptera: Geometridae) </span>coll. 19-APR-2022 on scrub oak, emerged 11-MAY-2022, leg. JC Andersen</p> <p>22-057B</p>
Telenomus alsophilae, FSCA 00060690
<p><em>Telenomus alsophilae</em> Viereck</p> <p>female, FSCA 00060690</p> <p>USA: MA: AXK: Almanac Pond, 41.28356566N, -70.00078497E, ex. eggs of <em>Alsophila pometaria </em>(Lepidoptera: Geometridae) coll. 19-APR-2022 on scrub oak, emerged 23-MAY-2022, leg. JC Andersen</p> <p>22-057I</p>
Telenomus alsophilae, FSCA 00061241
<p><em>Telenomus alsophilae</em> Viereck</p> <p>female, FSCA 00061241</p> <p>USA: MA: AXK: Almanac Pond, 41.28356566N, -70.00078497E, ex. eggs of <em>Alsophila pometaria</em> (Lepidoptera: Geometridae) coll. 19-APR-2022 on scrub oak, emerged 19-MAY-2022, leg. JC Andersen</p> <p>22-050C</p>
Fig. 11. Genitalia 3 in Telenomus alecto (Crawford) (Hymenoptera: Scelionidae), parasitoid of Diatraea magnifactella Dyar (Lepidoptera: Crambidae) from Jalisco, Mexico: a study based on morphological and molecular evidence
Fig. 11. Genitalia 3 (CIBE 18-029).
Telenomus euproctidis Wilcox, holotype female, USNMENT01109316
<p>GipMothLab 3348.12/15/10</p> <p>♀</p> <p>Ex. eggs from Japan-species?</p> <p>Ex eggs Euproctis conspersa 12-15-10</p> <p>Telenomus euproctidis Wilcox</p> <p>TypeNo 23067 USNM</p>
Telenomus sechellensis, FSCA 00051806
<p><em>Telenomus sechellensis</em></p> <p>FSCA 00051806</p> <p>RBX Lab Culture, Gqeberha, RSA, 5-II-2024, Dr. Geman Mulcahy, specimens sourced from lab, likely found on macademia farms in Limpopo or Mpumalanga, RSA</p>
Telenomus sechellensis Paratype female, NHMUK012858972
<p><em>Telenomus sechellensis</em></p> <p>Paratype female, NHMUK012858972</p> <p>[85] [Mahe ‘08-9. Seychelles Exp.] [Seychelle Islands. Percy Sladen Trust Expedition 1913-170.] [Telenomus seychellensis. J.J. Kieffer. Paratype.]</p>
Telenomus sechellensis FSCA 00060556
<p><em>Telenomus sechellensis </em>FSCA 00060556</p> <p>RBX Lab Culture, Gqeberha, RSA, 5-II-2024, Dr. Geman Mulcahy, specimens sourced from lab, likely found on macademia farms in Limpopo or Mpumalanga, RSA</p>
Telenomus sechellensis FSCA 00060557
<p><em>Telenomus sechellensis </em>FSCA 00060557</p> <p>RBX Lab Culture, Gqeberha, RSA, 5-II-2024, Dr. Geman Mulcahy, specimens sourced from lab, likely found on macademia farms in Limpopo or Mpumalanga, RSA</p>
Telenomus cristatus Johnson, holotype female, FSCA 00060143
<p><em>Telenomus cristatus </em>Johnson, holotype female, FSCA 00060143</p> <p>[St. Johns Bluff Duval Co., FLA.] [E. E. Grissell 30-VIII-1978 Collection] [HOLOTYPE Telenomus cristatus Johnson 1982]</p>
Telenomus wullschlegeli Mayr, lectotype female, NHMW-HYM#0005398
<p><em>Telenomus wullschlegeli </em>Mayr, 1879: 701, 702, 711</p>
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