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227 results for “Aphidiinae”
FIGURE 5 in Parasitoids (Hymenoptera: Braconidae: Aphidiinae) attacking aphids feeding on Prunoideae and Maloideae crops in Southeast Europe: aphidiine-aphid-plant associations and key
FIGURE 5. Labial palpi of A. transcaspicus Telenga (female).
FIGURE 1 in A new species of Acanthocaudus Smith (Braconidae: Aphidiinae), with a key to species and new host and distribution records for aphidiines associated with Silphium perfoliatum L. (Asterales: Asteraceae)
FIGURE 1. Lateral habitus, Acanthocaudus bicolor Kula, new species, based on type series.
Figure 5 from: Kim S, Tomanović Ž, Yu Y, Sohn J, Han Y, Lee G, Kim H (2021) Three new species of the genus Aphidius (Hymenoptera, Braconidae, Aphidiinae) from South Korea. Journal of Hymenoptera Research 86: 63-77. https://doi.org/10.3897/jhr.86.70767
Figure 5 Aphidius areolatus Ashmead, female A body B wing C antennae D head E propodeum F dorsal view of petiole G lateral view of petiole.
Figure 4 from: Kim S, Tomanović Ž, Yu Y, Sohn J, Han Y, Lee G, Kim H (2021) Three new species of the genus Aphidius (Hymenoptera, Braconidae, Aphidiinae) from South Korea. Journal of Hymenoptera Research 86: 63-77. https://doi.org/10.3897/jhr.86.70767
Figure 4 Aphidius asiaticus Kim & Tomanović, sp. nov., female A body B wing C antennae D head E propodeum F dorsal view of petiole G lateral view of petiole.
Figure 2 from: Kim S, Tomanović Ž, Yu Y, Sohn J, Han Y, Lee G, Kim H (2021) Three new species of the genus Aphidius (Hymenoptera, Braconidae, Aphidiinae) from South Korea. Journal of Hymenoptera Research 86: 63-77. https://doi.org/10.3897/jhr.86.70767
Figure 2 Aphidius longicarpus Kim & Tomanović, sp. nov., female A body B wing C antennae D head E propodeum F dorsal view of petiole G lateral view of petiole.
Figure 3 from: Kim S, Tomanović Ž, Yu Y, Sohn J, Han Y, Lee G, Kim H (2021) Three new species of the genus Aphidius (Hymenoptera, Braconidae, Aphidiinae) from South Korea. Journal of Hymenoptera Research 86: 63-77. https://doi.org/10.3897/jhr.86.70767
Figure 3 Aphidius longistigmus Kim & Tomanović, sp. nov., female A body B wing C antennae D head E propodeum F dorsal view of petiole G lateral view of petiole.
Supplementary material 1 from: Kim S, Tomanović Ž, Yu Y, Sohn J, Han Y, Lee G, Kim H (2021) Three new species of the genus Aphidius (Hymenoptera, Braconidae, Aphidiinae) from South Korea. Journal of Hymenoptera Research 86: 63-77. https://doi.org/10.3897/jhr.86.70767
Table S1
Figure 1 from: Kim S, Tomanović Ž, Yu Y, Sohn J, Han Y, Lee G, Kim H (2021) Three new species of the genus Aphidius (Hymenoptera, Braconidae, Aphidiinae) from South Korea. Journal of Hymenoptera Research 86: 63-77. https://doi.org/10.3897/jhr.86.70767
Figure 1 Neighbour-joining tree of 28 Aphidius spp. from South Korea based on their COI DNA barcode. Diaeretiella rapae was used for an outgroup.
Supplementary material 1 from: Kim S, Tomanović Ž, Petrović A, Čkrkić J, Lee G, Lim J, Kim H (2022) Toxares koreanus sp. nov. – a new Toxares species from South Korea (Hymenoptera, Braconidae, Aphidiinae). Journal of Hymenoptera Research 92: 185-198. https://doi.org/10.3897/jhr.92.84146
Figure S1
Figure 7 from: Mitrović M, Tomanović Ž (2018) New internal primers targeting short fragments of the mitochondrial COI region for archival specimens from the subfamily Aphidiinae (Hymenoptera, Braconidae). Journal of Hymenoptera Research 64: 191-210. https://doi.org/10.3897/jhr.64.25399
Figure 7 Scheme with overview of PCR attempts to recover the barcoding region of cytochrome c oxidase subunit I with novel primers from archival specimens from the genera Aphidius, Praon, Lysiphlebus, Ephedrus and Monoctonus. Primer pairs coloured red were used in direct PCR; black coloured primers were used in secondary nested reactions. Positions where short fragments within the subsequences overlap are marked with a pattern.
Figure 3 from: Mitrović M, Tomanović Ž (2018) New internal primers targeting short fragments of the mitochondrial COI region for archival specimens from the subfamily Aphidiinae (Hymenoptera, Braconidae). Journal of Hymenoptera Research 64: 191-210. https://doi.org/10.3897/jhr.64.25399
Figure 3 Agarose gel visualizing the products of direct PCR in initial trials testing the novel primers with fresh Praon samples. Three direct PCR reactions were conducted with primer pairs: 1. LCO1490/Pr1Rd, 2. Pr2Fd/Pr2Rd, 3. Pr3Fd/HCO2198. The species included in trials are PF1- P. volucre, PF2- P. dorsale, PF3- P. abjectum; M – marker.
Figure 6 from: Mitrović M, Tomanović Ž (2018) New internal primers targeting short fragments of the mitochondrial COI region for archival specimens from the subfamily Aphidiinae (Hymenoptera, Braconidae). Journal of Hymenoptera Research 64: 191-210. https://doi.org/10.3897/jhr.64.25399
Figure 6 Agarose gel visualizing the products of nested trials with products of direct PCR for samples LD8 – L. confusus, LD9 – L. desertorum; LD12 – L. fabarum; and LD13 – L. alpinus. The products of LD8 and LD9 from PCR with LCO1490/Lys1Rd were submitted to secondary reactions combining two primer pairs, viz., 1. LCO1490/Lys1Rn; and 2. Lys1Fn/Lys1Rd. Amplicons of LD8, LD9 and LD12 obtained with Aph2Fd/Lys2Rd were submitted to secondary nested trials with primer pairs Aph2Fd/Lys2Rn and Lys2Fn/Lys2Rd. Products from direct PCR with Lys3Fd/HCO2198 were used as the template for nested reactions with Lys3Fd/Aph3Rn and Lys3Fn/HCO2198.
Figure 5 from: Mitrović M, Tomanović Ž (2018) New internal primers targeting short fragments of the mitochondrial COI region for archival specimens from the subfamily Aphidiinae (Hymenoptera, Braconidae). Journal of Hymenoptera Research 64: 191-210. https://doi.org/10.3897/jhr.64.25399
Figure 5 Agarose gel visualizing the products of direct PCR in initial trials testing the novel primers with fresh Lysiphlebus samples. Tested combinations of primers were: 1) LCO1490/Lys1Rd; 2) Aph2Fd/Lys2Rd; 3) Pr2Fd/Lys2Rd; and 4) Lys3Fd/HCO2198. The species included in trials were: LF1 - L. hirticornis; LF2 - L. cardui; and LF3 - L. fabarum; M – marker.
Figure 4 from: Mitrović M, Tomanović Ž (2018) New internal primers targeting short fragments of the mitochondrial COI region for archival specimens from the subfamily Aphidiinae (Hymenoptera, Braconidae). Journal of Hymenoptera Research 64: 191-210. https://doi.org/10.3897/jhr.64.25399
Figure 4 Agarose gel visualizing the products of nested trials with products of direct PCR for samples PD12 - P. barbatum, PD14 - P. yomenae, and PD15 - P. yomenae. The products from PCR with Pr2Fd/Pr2Rd were submitted to secondary nested trials with primer pairs Pr2Fd/Pr2Rn and Aph2Fn/Pr2Rd. Amplicons obtained with Pr3Fd/HCO2198 were used as the template for nested reactions with Pr3Fd/Pr3Rn and Pr3Fn/HCO2198.
Figure 1 from: Mitrović M, Tomanović Ž (2018) New internal primers targeting short fragments of the mitochondrial COI region for archival specimens from the subfamily Aphidiinae (Hymenoptera, Braconidae). Journal of Hymenoptera Research 64: 191-210. https://doi.org/10.3897/jhr.64.25399
Figure 1 Position of internal degenerative primers within the barcoding region of COI. Aphidius - specific primers: Aph1Fn, Aph1Rn, Aph1Rd, Aph2Fd, Aph2Fn, Aph2Rn, Aph2Rd, Aph3Fd, Aph3Fn and Aph3Rn; Lysiphlebus - specific primers: Lys1Fn, Lys1Rd, Lys2Fn, Lys2Rn, Lys2Rd, Lys3Fd and Lys3Fn; Praon - specific primers: Pr1Fn, Pr1Rn, Pr1Rd, Pr2Fd, Pr2Rn, Pr2Rd, Pr3Fd, Pr3Fn and Pr3Rn. Arrows refer to the direction of the primers, forward or reverse. The exact position of internal primers is designated in comparison to the first nucleotide of the forward LCO1490 primer sequence (5' GGTCAACAAATCATAAAGATATTGG 3').
Figure 2 from: Mitrović M, Tomanović Ž (2018) New internal primers targeting short fragments of the mitochondrial COI region for archival specimens from the subfamily Aphidiinae (Hymenoptera, Braconidae). Journal of Hymenoptera Research 64: 191-210. https://doi.org/10.3897/jhr.64.25399
Figure 2 Agarose gel visualizing the products of direct PCR in initial trials testing the novel primers with fresh Aphidius samples. Three direct PCR reactions were conducted with the following primer pairs: 1 LCO1490/Aph1Rd 2 Aph2Fd/Aph2Rd; and 3 Aph3Fd/HCO2198. The species included in trials were: AF1- A. tanacetarius, AF2- A. sussi, AF3- A. sonchi, AF4- A. linosiphonis and AF5- A. ribis. M – marker.
Figure 8 from: Mitrović M, Tomanović Ž (2018) New internal primers targeting short fragments of the mitochondrial COI region for archival specimens from the subfamily Aphidiinae (Hymenoptera, Braconidae). Journal of Hymenoptera Research 64: 191-210. https://doi.org/10.3897/jhr.64.25399
Figure 8 The evolutionary history was inferred by using the Maximum Likelihood method based on the Tamura-Nei model. The tree with the highest log likelihood is shown. There were a total of 568 positions in the final dataset. Initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using the Maximum Composite Likelihood (MCL) approach, and then selecting the topology with superior log likelihood value. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The percentage of replicate trees >50% in which the associated taxa clustered together in the bootstrap test (500 replicates) are shown next to the branches.
Figure 3 from: Tian H-W, van Achterberg C, Chen X-X (2018) The genera Areopraon Mackauer, 1959 and Pseudopraon Starý, 1975 (Hymenoptera, Braconidae, Aphidiinae) from China, with keys to species. ZooKeys 780: 61-70. https://doi.org/10.3897/zookeys.780.26264
Figure 3 Pseudopraonhei Tian & Chen, sp. n. A head, anterior aspect B head, dorsal aspect C mesonotum, dorsal aspect D propodeum, dorsal aspect ET1, dorsal aspect F habitus, lateral aspect G fore wing H antennae I hind wing J ovipositor & ovipositor sheath, lateral aspect K metasoma, lateral aspect L mesosoma, lateral aspect. Scale bars: 0.2 mm.
Figure 2 from: Tian H-W, van Achterberg C, Chen X-X (2018) The genera Areopraon Mackauer, 1959 and Pseudopraon Starý, 1975 (Hymenoptera, Braconidae, Aphidiinae) from China, with keys to species. ZooKeys 780: 61-70. https://doi.org/10.3897/zookeys.780.26264
Figure 2 Areopraonchui Tian & Chen, sp. n. A fore wing B hind wing C mesosoma, lateral aspect D mesoscutum, dorsal aspect E metasoma, lateral aspect FT1, dorsal aspect G head, anterior aspect H head, dorsal view I antenna J propodeum, dorsal aspect K ovipositor sheaths, dorsal aspect.
Figure 4 from: Mitrović M, Starý P, Jakovljević M, Petrović A, Žikić V, Pérez Hidalgo N, Tomanović Ž (2019) Integrative taxonomy of root aphid parasitoids from the genus Paralipsis (Hymenoptera, Braconidae, Aphidiinae) with description of new species. ZooKeys 831: 49-69. https://doi.org/10.3897/zookeys.831.31808
Figure 4 Phylogenetic relationship inferred using the maximum parsimony (MP) method. The consistency index is (0.533333), the retention index is (0.681818), and the composite index is 0.476540 (0.363636) for all sites and parsimony-informative sites. The MP tree was obtained using the subtree-pruning-regrafting (SPR) algorithm with search level 1, in which the initial trees were obtained by the random addition of sequences (10 replicates). The percentage of replicate trees in which >50% of the associated taxa clustered together in the bootstrap test (500 replicates) is shown next to the branches (in red color). Since the topology is identical, the bootstrap support of branches obtained by the maximum likelihood method is presented in black color as well. Barcoding haplotypes of the analyzed archival Paralipsis specimens are designated with codes from PH1 to PH14, species name, host aphid and host plant. Abbreviations for the countries of origin are as follows: GER – Germany; FRA – France; SRB – Serbia; LIT – Lithuania; CR – Czech Republic; MOL – Moldova; MOR – Morocco; and ESP – Spain.
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