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132 results for “Cotesia”
Fig. 31. A–B in Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species
Fig. 31. A–B. Cotesia urabae Austin & Allen, 1989, paratype, ♀ (WINC). A. Habitus in dorsal view. B. Fore wing. C–E. Cotesia vestalis (Haliday, 1834), ♀ (WINC). C. Head in dorsal view and anteromesoscutum. D. Propodeum and dorsal metasoma E. Fore wing.
Fig. 34. A in Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species
Fig. 34. A. Fore wing terminology, abbreviation: pt = pterostigma. B. General morphological terminology, abbreviations: ams = anteromesoscutum, mt = metanotum, pp = propodeum, sc = scutellum (also referred to as the mesoscutellum), sd = scutellar disk, ss = scutellar sulcus, T1 = first metasomal tergite, T2 = second metasomal tergite, T3 = third metasomal tergite.
Fig. 28 in Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species
Fig. 28. Cotesia rufiventris (Bingham, 1906), paralectotype, ♀ (NHMUK). A. Mesosoma in dorsal view and T1–3 B. Habitus in dorsal view and fore wing C. Habitus in lateral view.
Fig. 27 in Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species
Fig. 27. Cotesia ruficrus (Haliday, 1834), ♀ (ANIC 32 130230) A. Habitus in lateral view. B. Habitus in dorsal view. C. Fore wing.
Fig. 25 in Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species
Fig. 25. Cotesia reidarum sp. nov., holotype, ♀ (QM T246703). A. Habitus in dorsal view. B. Habitus in lateral view. C. Head in dorsal view. D. Head in anterior view. E. Propodeum. F. Fore wing.
Fig. 22 in Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species
Fig. 22. Cotesia ocellata sp. nov., holotype, ♀ (SAMA 32-44404). A. Head in dorsal view and anteromesoscutum. B. Habitus in lateral view. C. T1–3. D. Habitus in dorsal view. E. Head in anterior view. F. Mesoscutum and propodeum. G. Fore wing.
Spontaneous parthenogenesis in the parasitoid wasp Cotesia typhae: low frequency anomaly or evolving process?
<p>Raw data linked to the manuscript, including phenotyping and genotyping results for all Cotesia typhae females analyzed in this study.</p>
Figs 1–6 in Cotesia Pappi Sp. N. (Hymenoptera, Braconidae: Microgastrinae) From Turkey
Figs 1–6. Cotesia pappi sp. n.: 1 = head in dorsal view, 2 = 15–18th joints of antenna, 3 = hind tibia and tarsal joints, 4 = fore wing, 5 = hind wing, 6= basal tergite. Scale bar 0.5 mm
Figs. 2−7. Cotesia dictyoplocae. 2 in First report of Cotesia dictyoplocae (Hymenoptera: Braconidae), a larval parasitoid of Antheraea assamensis (Lepidoptera: Saturniidae), from India
Figs. 2−7. Cotesia dictyoplocae. 2, Body in habitus; 3, head in frontal view; 4, propodeum; 5, wings; 6, mesosoma with metasoma in part; 7, metasoma with propodeum.
Fig. 2 in Three new species and two new records of the genus Cotesia Cameron (Hymenoptera: Braconidae) from Iran
Fig. 2. Cotesia khuzestanensis Zargar & Gupta sp. nov., ICAR-NBAIR/NIM/MICROG/COT/451611. A. Head, frontal view. B. Head, dorsal view. C. Mesosoma, dorsal view. D. Fore wing. E. Metasoma, dorsal view. F. Habitus, lateral view.
Fig. 4 in Three new species and two new records of the genus Cotesia Cameron (Hymenoptera: Braconidae) from Iran
Fig. 4. Cotesia cynthiae (Nixon, 1974). A. Head, frontal view., ICAR-NBAIR/NIM/MICROG/ COT/3416. B. Head, dorsal view. C. Mesosoma, dorsal view. D. Fore wing. E. Metasoma, dorsal view. F. Habitus, lateral view.
Fig. 3 in Three new species and two new records of the genus Cotesia Cameron (Hymenoptera: Braconidae) from Iran
Fig. 3. Cotesia zagrosensis Zargar & Gupta sp. nov., ICAR-NBAIR/NIM/MICROG/COT/6717. A. Head, frontal view. B. Head, dorsal view. C. Mesosoma, dorsal view. D. Fore wing. E. Metasoma, dorsal view. F. Habitus, dorsal view.
Fig. 5 in Three new species and two new records of the genus Cotesia Cameron (Hymenoptera: Braconidae) from Iran
Fig. 5. Cotesia glabrata (Telenga, 1955), ICAR-NBAIR/NIM/MICROG/COT/20416. A. Head, frontal view. B. Head, dorsal view. C. Mesosoma, dorsal view. D. Fore wing. E. Metasoma, dorsal view. F. Habitus, lateral view.
Fig. 1 in Cotesia invirae, sp. nov., from South Brazil: a new gregarious microgastrine wasp (Hymenoptera: Braconidae) reared from Opsiphanes invirae (Nymphalidae) feeding on palms
Fig. 1. (a) Lateral view of female Cotesia invirae; (b) view of the labrum, mandibles and labial palps; (c) front view of the face; (d) lateral view of the antenna; (e) dorsal view of the mesosoma; (f) dorsal view of abdomen; (g) view of the forewing in situ; (h) details of the spurs of the tibia (inner and outer); (i) larvae of C. invirae; (j) front view of the pupa of C. invirae; (k) dorsal view of pupa of C. invirae; (l) lateral view of the pupa of C. invirae; (m) front view of head, the larvae of C. invirae; (n) view of the cocoons of C. invirae, arranged regularly and secured with silk threads to each other in the form of palisades on the host. Some material here previously reported in Salgado-Neto (2013) as from C. alius.
Fig. 1. Neighbor-joining tree generated under the Kimura 2 in Cotesia flavipes (Hymenoptera: Braconidae) as a biological control agent of sugarcane stem borers in Colombia's Cauca River Valley
Fig. 1. Neighbor-joining tree generated under the Kimura 2-parameter (K2P) nucleotide substitution model. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1,000 replicates) is shown next to the branches. Abbreviations for sugarcane mills in Colombia's Cauca River Valley are as follows: Manuelita (MN), Mayagüez (MY), Pichichí (PC), Providencia (PV), Riopaila (RP), Risaralda (RS), Sancarlos (SC). GeneBank C. flavipes accessions:Uganda - JQ396735.1, Brazil - DQ232320.1, India - DQ232336.1, Kenya - DQ232317, Thailand - DQ232340.1, USA - DQ232330.1, South Pakistan - JQ396714.1, Jamaica - DQ232321.1, Pakistan - DQ232335.1, Sri Lanka - DQ232327.1, Indonesia - DQ232337.1, Mauritius - DQ232319.1, Reunion - DQ232329.1, Papua New Guinea - DQ232316.1.
Fig. 2 in Cotesia flavipes (Hymenoptera: Braconidae) as a biological control agent of sugarcane stem borers in Colombia's Cauca River Valley
Fig. 2. Distribution of Cotesia flavipes in different sugarcane mills of Colombia's Cauca River Valley.
Fig. 5 in Approaches for assessing the impact of Zea mays (Poaceae) on the behavior of Spodoptera frugiperda (Lepidoptera: Noctuidae) and its parasitoid Cotesia marginiventris (Hymenoptera: Braconidae)
Fig. 5. Spodoptera frugiperda moths prefer to oviposit on uninfested Zea mays plants. To test the effect of prior infestation with S. frugiperda (FAW) compared to a non-treated (NT) control plant on S. frugiperda oviposition preference, a pair-wise oviposition assay was performed using 3 independent experiments (Experiments 1–3). In each experiment, 6 uninfested plants and 6 infested plant treatments were used, and egg masses on each plant counted (Table). The total number of egg masses on each treatment was determined and from these data the percent total oviposition (%NT and %infested plant) calculated. The graph shows the mean (± SE) percent parasitism for each treatment,and the treatments were statistically significantly different using a pair-wise t-test: P ≤ 0.05; n = 3.
Fig. 6. Cotesia marginiventris wasps have a in Approaches for assessing the impact of Zea mays (Poaceae) on the behavior of Spodoptera frugiperda (Lepidoptera: Noctuidae) and its parasitoid Cotesia marginiventris (Hymenoptera: Braconidae)
Fig. 6. Cotesia marginiventris wasps have a marginal preference to oviposit on Spodoptera frugiperda on W22 compared to B104 Zea mays inbred plants. To test the effect of different Z. mays varieties on oviposition preference of C. marginiventris, a pair-wise oviposition assay was performed using 13 independent experiments (Experiments 1–13). In each experiment, the number of S. frugiperda larvae recovered from B104 or W22 genotypes that were parasitized by C. marginiventris (P), not-parasitized (NP), or had died shortly afer collection (D), and the percentage of larvae parasitized was calculated by (P/[P + NP]) × 100 for each plant variety (Table). Experiments that had less than 5 parasitized larvae or more than 15 dead (bold) were discarded. The graph shows mean (± SE) percentage parasitism for each treatment. The treatments were not significantly different using a pair-wise t-test with P ≤ 0.05 and n = 8.
Fig. 3 in Approaches for assessing the impact of Zea mays (Poaceae) on the behavior of Spodoptera frugiperda (Lepidoptera: Noctuidae) and its parasitoid Cotesia marginiventris (Hymenoptera: Braconidae)
Fig. 3. Stages of Cotesia marginiventris development. Representative images of C. marginiventris adult (A), larva emerging from S. frugiperda host (B) and pupae (C) are shown. Size bars are 20 µm.
Fig. 4 in Approaches for assessing the impact of Zea mays (Poaceae) on the behavior of Spodoptera frugiperda (Lepidoptera: Noctuidae) and its parasitoid Cotesia marginiventris (Hymenoptera: Braconidae)
Fig. 4. Larval growth assays of Spodoptera frugiperda. Two independent larval growth assays for S. frugiperda on the Zea mays inbred line B104. Graph shows mean larval weights (± SE) from 3 to 7 d afer infestation, n = (35–100). Because these growth assays were done at different times, they were not statistically compared.
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