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13 results for “Doryctobracon”
FIGURE 7. Comparison concatenated tree ITS2 – 28S rDNA D2 in Description of two new species closely related to Doryctobracon areolatus (Szépligeti, 1911) (Hymenoptera, Braconidae), based on morphometric and molecular analyses
FIGURE 7. Comparison concatenated tree ITS2 – 28S rDNA D2 (UPGMA) produced from the nucleotide sequences (A), cluster analysis of the Mahalanobis distance (UPGMA) calculated from the shape of the wings components (B). (DAAP = Doryctobracon areolatus from Amapá, DAGO = D. areolatus from Goiás, DATO = D. areolatus from Tocantins, DASP = D. areolatus from São Paulo, YSAP = Doryctobracon whartoni sp. nov. (yellow stigma) from Amapá; BSAP = Doryctobracon adaimei sp. nov. (brown stigma) from Amapá, BSGO = D. adaimei sp. nov. from Goiás, BSTO = D. adaimei sp. nov. from Tocantins.
FIGURE 3 in Description of two new species closely related to Doryctobracon areolatus (Szépligeti, 1911) (Hymenoptera, Braconidae), based on morphometric and molecular analyses
FIGURE 3. Fore wing. (A) Doryctobracon whartoni sp. nov. (yellow stigma); (B) Doryctobracon adaimei sp. nov. (brown stigma).
FIGURE 8 in Description of two new species closely related to Doryctobracon areolatus (Szépligeti, 1911) (Hymenoptera, Braconidae), based on morphometric and molecular analyses
FIGURE 8. Phylogeny reconstruction for Doryctobracon species inferred by using the maximum likelihood and Neighborjoining methods using sequences from the molecular markers ITS2 (A), 28S-D2 (B) and their concatenated sequences (C). ML tree with the highest log likelihood (-1065.5986) and the optimal NJ tree with the sum of branch length (=0.13197667) shown for the ITS2 sequences were based on the Tamura 3-parameter model (Tamura, 1992); ML tree with the highest log likelihood (-719.5043) and the optimal NJ tree with the sum of branch length (=0.11870754) shown for the 28S-D2 sequences were based on the Tamura 3-parameter model; the ML tree with the highest log likelihood (-1598.9138) and the optimal NJ tree with the sum of branch length (=0.076130) for the concatenated ITS2 and 28S-D2 sequences was based, respectively, on the Tamura 3- parameter model+G (=0.1096)+I (=0.001%) and Tamura 3-parameter model+G (=0.1).
FIGURE 4 in Description of two new species closely related to Doryctobracon areolatus (Szépligeti, 1911) (Hymenoptera, Braconidae), based on morphometric and molecular analyses
FIGURE 4. Doryctobracon whartoni sp. nov. head, front view (A), mesosoma, smooth notaulices, dorsal view (B), head and mesosoma, smooth mesopleura (C), setaceous propodeum, dorsal view (D), ovipositor apex (E), pattern of ovipositor sheath bristles (F).
FIGURE 2 in Description of two new species closely related to Doryctobracon areolatus (Szépligeti, 1911) (Hymenoptera, Braconidae), based on morphometric and molecular analyses
FIGURE 2. Landmarks on fore wing of Doryctobracon areolatus. 1. base of vein costal; 2. Intersection of the parastigma, 1RS and wing margin; 3. Intersection of the end of stigma and R1a; 4. Intersection of the radial sector 3RSb and wing margin; 5. Intersection of vein 3M and wing margin; 6. Intersection of vein 3CU and wing margin; 7. Intersection of vein 3-1A and wing margin; 8. Intersection of the veins 3-1A and 2cu-a; 9. Intersection of the veins 2CUa, 3CU and 2cu-a; 10. Intersection of the veins 1-1A, 1cu-a and 2-1A; 11. Intersection of the veins 1-1A and base of wing; 12. Intersection of the veins M+CU, 1M and 1CU; 13. Intersection of the veins M+CU, 1cu-a and 1CU; 14 Intersection of the veins 2CUa, 1CU and 1m-cu; 15. Intersection of the veins 2M, r-m and 3M; 16. Intersection of the veins 1m-cu, (RS+M)a, 2RS and 2M; 17. Intersection of the veins 1M, (RS+M)a and 1RS; 18. Intersection of the veins 3RSa, 3RSb and r-m; 19. Intersection of the veins 3RSa, r and 2RS; 20. Intersection of the vein r and base of stigma (venational terminology according to Sharkey & Wharton 1997).
FIGURE 6 in Description of two new species closely related to Doryctobracon areolatus (Szépligeti, 1911) (Hymenoptera, Braconidae), based on morphometric and molecular analyses
FIGURE 6. Dispersion graphic of Doryctobracon areolatus males and females from Amapá (DAAP), Tocantins (DATO), Goiás (DAGO) and São Paulo (DASP); Doryctobracon whartoni sp. nov. yellow stigma, Amapá (YSAP); Doryctobracon adaimei sp. nov. brown stigma, Amapá (BSAP) and Goiás (BSGO) in the bidimensional space of canonical variables VC1 and VC2. The deformations diagrams indicate the presumable wing conformations for individuals in the superior and inferior ends of the canonical variables. Deformation magnitudes were amplified 3x for visualization.
FIGURE 1 in Description of two new species closely related to Doryctobracon areolatus (Szépligeti, 1911) (Hymenoptera, Braconidae), based on morphometric and molecular analyses
FIGURE 1. Chromatic variation on the wings and legs. Doryctobracon areolatus (A-A2), Doryctobracon whartoni sp. nov. (yellow stigma – YS) (B-B2), Doryctobracon adaimei sp. nov. (Goiás) (C-C2), D. adaimei sp. nov. (Tocantins) (D-D2), D. adaimei sp. nov. (Amapá) (brown stigma – BS) (E-E2). (the figures are not on the same scale).
FIGURE 5 in Description of two new species closely related to Doryctobracon areolatus (Szépligeti, 1911) (Hymenoptera, Braconidae), based on morphometric and molecular analyses
FIGURE 5. Doryctobracon adaimei sp. nov. head, front view (A), mesosoma smooth notaulices, dorsal view (B), head and mesosoma smooth mesopleura (C), propodeum, dorsal view (D), dorsal view of the petiole (E), modified spiracle (F), ovipositor apex (G), pattern of ovipositor sheath bristles (H).
Figure 1 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 1 Duration of development of non-diapausing and diapausing Doryctobracon areolatus females and males, parasitizing Anastrepha ludens larvae.
Figure 5 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 5 Net fecundity of Doryctobracon areolatus females from A non-diapausing and B diapausing cohorts.
Figure 3 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 3 Canonical analysis of adult parasitoids' morphological data from non-diapausing and diapausing Doryctobracon areolatus. A Comparison by type of development B comparison among females C comparison between sexes. The asterisk (*) indicates a significant difference.
Figure 2 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 2 Canonical analysis of morphological data from puparia containing non-diapausing and diapausing male and female Doryctobracon areolatus parasitoids. The asterisk (*) indicates a significant difference.
Figure 4 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 4 Female survival of Doryctobracon areolatus parasitoids in the fecundity bioassays.
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