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Fig. 45 in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 45. Glyptapanteles mouldsi Fagan-Jeffries, Bird & Austin sp. nov., paratypes, ♀. A–F. QM T250978. G. QM T250979. A. Lateral habitus. B. Fore wing. C. Dorsal mesosoma. D. Anterior head. E. Lateral head. F. Dorsal metasoma. G. Dorsal head.
Fig. 44. Glyptapanteles mnesampela Austin, 2000 in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 44. Glyptapanteles mnesampela Austin, 2000 holotype, ♀ (ANIC 32-141445). A. Lateral habitus. B. Dorsal propodeum and metasoma. C. Anterior head. Images courtesy of O. Evangelista (ANIC).
Fig. 36 in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 36. Glyptapanteles goodwinnoakes Fagan-Jeffries, Bird & Austin sp. nov., paratype, ♀ (QM T250956). A. Lateral habitus. B. Dorsal head. C. Anterior head. D. Dorsal habitus. E. Fore wing. F. Lateral head.
Fig. 29 in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 29. Glyptapanteles doreyi Fagan-Jeffries, Bird & Austin sp. nov., paratype, ♀ (ANIC 32 130330), 'clade B'. A. Lateral habitus. B. Fore wing. C. Dorsal head. D. Dorsal metasoma. E. Anterior head. F. Lateral head. G. Dorsal mesosoma.
Fig. 7. A in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 7. A. Glyptapanteles harveyi Fagan-Jeffries, Bird & Austin sp. nov., paratype, ♀ (WAM E109889), arrow indicating faint median carina at the posterior end of the propodeum. B. G. kittelae Fagan-Jeffries, Bird & Austin sp. nov., holotype, ♀ (SAMA 32-46156), propodeum with median carina completely absent.
Fig. 8. A in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 8. A. Glyptapanteles andamookaensis Fagan-Jeffries, Bird & Austin sp. nov., holotype, ♀ (SAMA 32-035451), hind femur mostly dark. B. G. kittelae Fagan-Jeffries, Bird & Austin sp. nov., holotype, ♀ (SAMA 32-46156), hind femur mostly light brown.
Fig. 6. A. Glyptapanteles mnesampela Austin, 2000 in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 6. A. Glyptapanteles mnesampela Austin, 2000, holotype, ♀ (ANIC 32-141445), T1 and T2 pale. B. G. eburneus Fagan-Jeffries, Bird & Austin sp. nov., holotype, ♀ (AM K.517935), T1 and T2 pale. C. G. rixi Fagan-Jeffries, Bird & Austin sp. nov., holotype, ♀ (QM T250981), T2 pale, T1 darker than T2. D. G. mouldsi Fagan-Jeffries, Bird & Austin sp. nov., paratype, ♀, (QM T250978), T1 dark, T2 pale. E. G. dowtoni Fagan-Jeffries, Bird & Austin sp. nov., paratype, ♀ (QM T250953), T1 dark, T2 pale. F. G. harveyi Fagan-Jeffries, Bird & Austin sp. nov., paratype, ♀ (WAM E109889), T1 dark, T2 dark.
Fig. 5. A in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 5. A. Glyptapanteles albigena Fagan-Jeffries, Bird & Austin sp. nov., holotype, ♀ (ANIC 32 130334), arrow indicating a large pale gena spot. B. G. sanniopolus Fagan-Jeffries, Bird & Austin sp. nov., holotype, ♀ (ANIC 32 130370), arrow indicating a large pale gena spot. C. G. kittelae Fagan- Jeffries, Bird & Austin sp. nov., holotype, ♀ (SAMA 32-46156) arrow indicating small (clearly visible) pale gena spot. D. G. harveyi Fagan-Jeffries, Bird & Austin sp. nov., paratype, ♀ (WAM E109889), arrow indicating small (faint, barely visible) pale gena spot. E. G. baylessi Fagan-Jeffries, Bird & Austin sp. nov. paratype, ♀ (AM K.517936), gena without a pale spot.
Fig. 2 in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 2. Maximum likelihood phylogeny constructed using IQ-TREE ver. 1.6.12 of a concatenated COI and wingless alignment including Glyptapanteles Ashmead, 1904 from Australia, Papua New Guinea and Fiji, with specimens of Cotesia Cameron, 1891 from Australia included for contextual placement of the genus. Branch support values are given as SH-aLRT support (%) / ultrafast bootstrap support (%), with symbols representing value ranges as follows: * = 96–100; • = 91–95; ^ = 85–90; - = <85.
Fig. 3 in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 3. Known distribution of the described species of Glyptapanteles Ashmead, 1904 from Australia, represented by coloured circles or part circles, with each species represented by a different colour (see key to colours below map).
Fig. 4 in Systematic revision of the parasitoid wasp genus Glyptapanteles Ashmead (Hymenoptera: Braconidae: Microgastrinae) for Australia results in a ten-fold increase in species
Fig. 4. Distribution of species groups of Glyptapanteles Ashmead, 1904 in Australia. A. G. albigena species group. B. G. arcanus species group. C. G. austini species group. D. G. eburneus species group. E. G. mouldsi species group. F. G. niveus species group. G. Unplaced species of Glyptapanteles in Australia.
Native generalist natural enemies and an introduced specialist parasitoid together control an invasive forest insect
<p>Specialized natural enemies have long been considered a major force driving the population dynamics of outbreaking forest insects. While research has traditionally focused on the role of specialist parasitoids, recent studies and reviews reflect an appreciation of complex interactions among many regulatory factors. The sources suggest that specialist parasitoids and generalist predators can each inflict strong top‐down effects and that specialists and generalists can interact to regulate insect herbivore populations. Here we use the model study organism winter moth (<i>Operophtera brumata</i>) in its invasive range in the northeast United States to investigate interactions between the introduced, host-specific tachinid parasitoid <i>Cyzenis albicans</i> and native, generalist pupal predators. Prior research in Canada showed that predation of winter moth pupae increased after <i>C. albicans </i>establishment. To explain this phenomenon, the following hypotheses have been suggested: (1) parasitoids suppress the winter moth population to a density that can be maintained by generalist predators, (2) unparasitized pupae are preferred by predators and thus experience higher mortality rates, or (3) <i>C. albicans </i>sustain higher predator populations throughout the year more effectively than winter moth alone. We tested these hypotheses by deploying winter moth pupae over six years spanning 2005 to 2017 and by modeling pupal predation rates as a function of winter moth density and <i>C. albicans </i>establishment. We also compared predation rates of unparasitized and parasitized pupae and considered additional mortality by a native pupal parasitoid. We found support for the first hypothesis; we detected both temporal and spatial density dependence, but only in the latter years of the study when winter moth densities were lower. We found no evidence for the latter two hypotheses. Our findings suggest that pupal predators have a regulatory effect on winter moth populations only after populations have been reduced, presumably by the introduction of the host-specific parasitoid <i>C. albicans</i>.</p>
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>
Fig. 2 in A Review Of The Carpathian Ephialtini Parasitoids (Hymenoptera, Ichneumonidae, Pimplinae) Associated With Spiders
Fig. 2. Clistopyga, face (frontal view), Ơ: 1 — C. rufator; 2 — C. incitator; 3 — C. canadensis; 4 — C. sziladyi.
Fig. 4 in A Review Of The Carpathian Ephialtini Parasitoids (Hymenoptera, Ichneumonidae, Pimplinae) Associated With Spiders
Fig. 4. Schizopyga and Sinarachna, ♀. 1–5 — Schizopyga: 1 — S. coxator, habitus (lateral view); 2 — S. circulator, face (frontal view); 3 — S. coxator, face (frontal view); 4 — S. coxator, pronotum (lateral view); 5 — S. circulator, pronotum (lateral view); 6–7 — Sinarachna, tergites III–IV of metasoma (dorsal view): 6 — S. pallipes; 7 — S. nigricornis.
Fig. 3 in A Review Of The Carpathian Ephialtini Parasitoids (Hymenoptera, Ichneumonidae, Pimplinae) Associated With Spiders
Fig. 3. Polysphincta, ♀. 1–2 — metapleuron (lateral view): 1 — P. tuberosa; 2 — P. vexator; 3–5 — metasoma (dorsal view): 3 — P. tuberosa, tergites III–IV; 4 — P. rufipes, tergites II–IV; 5 — P. vexator, tergites II–IV.
FIG. 10 in High diversity of pimpline parasitoid wasps (Hymenoptera, Ichneumonidae, Pimplinae) from the lowermost Eocene Fur Formation (Denmark)
FIG. 10. — Holotype of Xanthopimpla ciboisae n. sp. (FUR-10046), photograph and interpretative drawing, where dotted lines represent uncertain and/or interpolated interpretations. Scale bar: 2 mm.
FIG. 7 in High diversity of pimpline parasitoid wasps (Hymenoptera, Ichneumonidae, Pimplinae) from the lowermost Eocene Fur Formation (Denmark)
FIG. 7. — Specimens of Epitheronia stigmatica (Henriksen, 1922), n. comb.: A, C, holotype, deposited at the Natural History Museum in Copenhagen; B, D, specimen MOL-MM-3141. Photographs (A, B), detail (E) and interpretative drawings (B, D), where dotted lines represent uncertain and/or interpolated interpretations. Scale bars: 2 mm.
FIG. 4 in High diversity of pimpline parasitoid wasps (Hymenoptera, Ichneumonidae, Pimplinae) from the lowermost Eocene Fur Formation (Denmark)
FIG. 4. — Holotype of Crusopimpla minuta n. sp. (FUR-13076), photograph (A), detail (B) and interpretative drawing (C), where dotted lines represent uncertain and/or interpolated interpretations. Scale bars: A, C, 1 mm; B, 0.5 mm.
FIG. 3 in High diversity of pimpline parasitoid wasps (Hymenoptera, Ichneumonidae, Pimplinae) from the lowermost Eocene Fur Formation (Denmark)
FIG. 3. — Holotype of Crusopimpla elongata n. sp. (FUR-11220), photograph (A) and interpretative drawing (B), where dotted lines represent uncertain and/or interpolated interpretations. Scale bar: 1 mm.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.