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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.
Text-fig. 4. a: Conglomeratic to massive sandstone facies 1, facies A are composed of Andesit (AF), Clay (CF) and Sandstone (SF) fragments lain on medium-sandstone. b: Conglomeratic to massive sandstone facies, outcropping of massive sandstone facies comprises of fine to medium grain size of grey to yellowish sandstone. c: Heterolithic sandstone-mudstone facies, intercalation of fine sand with silt and shale as type form of heterolithic sandstone mudstone as indicated by a high sand/shale ratio. d: Example outcrops of heterolithic sandstone-mudstone 2 indicated by low sand/shale ratio. e: Heterolithic fine sand and mudstone and mudstone facies, intercalation of thin sandstone and shale. f: Representative of slump deposits outcrops belong to conglomeratic to massive sandstone facies, which is indicated by the intercalation of sandstone and shale and some disturbed beds or layers as seen in slump deposits. The facies type is normally deposited within the basin floor, channel margin or as a product of the overbank deposits. In this figure the slump deposit is shown as internal bedding, some occurred on the bedding-plane. Trend slope measurement of the fold-axis revealed values N 135°E and N 108°E. in Lithofacies And Ichnofacies Of Turbidite Deposits, West Java, Indonesia
Text-fig. 4. a: Conglomeratic to massive sandstone facies 1, facies A are composed of Andesit (AF), Clay (CF) and Sandstone (SF) fragments lain on medium-sandstone. b: Conglomeratic to massive sandstone facies, outcropping of massive sandstone facies comprises of fine to medium grain size of grey to yellowish sandstone. c: Heterolithic sandstone-mudstone facies, intercalation of fine sand with silt and shale as type form of heterolithic sandstone mudstone as indicated by a high sand/shale ratio. d: Example outcrops of heterolithic sandstone-mudstone 2 indicated by low sand/shale ratio. e: Heterolithic fine sand and mudstone and mudstone facies, intercalation of thin sandstone and shale. f: Representative of slump deposits outcrops belong to conglomeratic to massive sandstone facies, which is indicated by the intercalation of sandstone and shale and some disturbed beds or layers as seen in slump deposits. The facies type is normally deposited within the basin floor, channel margin or as a product of the overbank deposits. In this figure the slump deposit is shown as internal bedding, some occurred on the bedding-plane. Trend slope measurement of the fold-axis revealed values N 135°E and N 108°E.
Text-fig. 14. a, b: Acer aff. campestre. a: Oriolo MSF 664. b: Oriolo MSF 666. c, d: Acer aff. monspessulanum. c: Oriolo MSF 641. d: Oriolo MSF 662. e: Acer aff. opulus subsp. obtusatum Oriolo MSF 669. f, g: Acer aff. cappadocicum subsp. lobelii. f: Oriolo MSF 675. g: Oriolo MSF 631. h, i: Cornus sp. Oriolo MSF 655, two views of a strongly folded leaf impression. Scale bars 50 mm (a, e–g), 10 mm (b–d, h, i). in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. 14. a, b: Acer aff. campestre. a: Oriolo MSF 664. b: Oriolo MSF 666. c, d: Acer aff. monspessulanum. c: Oriolo MSF 641. d: Oriolo MSF 662. e: Acer aff. opulus subsp. obtusatum Oriolo MSF 669. f, g: Acer aff. cappadocicum subsp. lobelii. f: Oriolo MSF 675. g: Oriolo MSF 631. h, i: Cornus sp. Oriolo MSF 655, two views of a strongly folded leaf impression. Scale bars 50 mm (a, e–g), 10 mm (b–d, h, i).
Dataset: Amicus Therapeutics, Inc. (FOLD) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Supplementary Simulation Data for "A contact-based analysis of local energetic frustration dynamics identifies key residues enabling RfaH fold-switch"
<p>Additional simulation data for "A contact-based analysis of local energetic frustration dynamics identifies key residues enabling RfaH fold-switch"</p> <p><strong>Content:</strong></p> <p>'clusters_foldswitch': Contains representative structures in PDB format of the refolding landscape of RfaH using all-atom structure-based models. The QA and QB values indicated in each filename correspond to the fraction of native contacts contain in the representative structure in comparison to the total number of contacts in the structure of the autoinhibited ⍺-folded (A) and active β-folded (B) states of the C-terminal domain of RfaH.</p> <p>'input_one_fs': Contains a trajectory of RfaH refolding from the ⍺-folded to the β-folded state, with each frame contained into a separate PDB file, totalling 400 PDB files. These files can be used with the frustration-based windowing method scripts and Colab notebook made available at https://github.com/pb3lab/RfaH-frustration</p> <p>'input_many_fs': Contains several trajectory of RfaH reversible refolding between the ⍺-folded and β-folded states, with each frame contained into a separate PDB file, totalling 11,999 PDB files. These files can be used with the frustration-based windowing method scripts and Colab notebook made available at https://github.com/pb3lab/RfaH-frustration</p> <p>'output_one_fs': Contains output results from the analysis of local energetic frustration dynamics of the 400 frames contained in 'input_one_fs' using the windowing method available in the Colab notebook at https://github.com/pb3lab/RfaH-frustration.</p> <p>'output_many_fs': Contains output results from the analysis of local energetic frustration dynamics of the 11,999 frames contained in 'input_many_fs' using the windowing method available in the Python script at https://github.com/pb3lab/RfaH-frustration.</p>
Figure 1 in Factors affecting the number of leaves included in the shelters of the leaf-folding caterpillar, Vanessa indica (Lepidoptera: Nymphalidae)
Figure 1. Leaf shelters of Vanessa indica larvae: (A) a one-leaf shelter of a later instar; (B) a two-leaf shelter of a later instar, a gap in the shelter surface was covered with a part of another leaf; (C) a two-leaf shelter of an early instar; (D) a one-leaf shelter of an early instar, the shelter was not folded fully, and a gap was covered with silk threads. Scale bars are 20 mm.
Figure 3 in Factors affecting the number of leaves included in the shelters of the leaf-folding caterpillar, Vanessa indica (Lepidoptera: Nymphalidae)
Figure 3. The number of leaves used was compared between untrenched (U) and trenched (T) shelters with Mann-Whitney U test (*p <0.05; NS, not significant). Sample sizes are shown in Table 3. No shelters of first instar larvae had trenches.
Figure 4 in Two-fold increase in White Stork (Ciconia ciconia) population in Lithuania: a consequence of changing agriculture?
Figure 4. Proportion of White Stork nests built in different tree species (% of all nests in trees).
Fig. 7 in Suraqalatia Brasieri Görmuş, Lawa & Nuaimy, 2017 (Larger Benthic Foraminifera; Suraqalatiidae N. Fam.) From The Late Maastrichtian Of The Tarbur Formation (Zagros Fold-Thrust-Belt) And Remarks On Dicyclina Munier-Chalmas, 1887
Fig. 7 Dicyclina schlumbergeri Munier-Chalmas, Late Maastrichtian Tarbur Formation of the Naghan section. a–b Oblique equatorial sections showing embryonic chamber, kidney-shaped in outline. Note the presence of primary partitions only (arrows). c Oblique section of a juvenile specimen. d, f Partial, slightly oblique axial sections. e Fragmentary equatorial section. Scale bars = 1 mm. Thin-sections: 2NG 191 (a), NG 83 (b), NG 13-1 (c), NG 34 (d), NG 49 (e), 2NG 34 big (f).
Fig. 3 in Suraqalatia Brasieri Görmuş, Lawa & Nuaimy, 2017 (Larger Benthic Foraminifera; Suraqalatiidae N. Fam.) From The Late Maastrichtian Of The Tarbur Formation (Zagros Fold-Thrust-Belt) And Remarks On Dicyclina Munier-Chalmas, 1887
Fig. 3 Suraqalatia brasieri Görmüş, Lawa & Al Nuaimy, upper Maastrichtian Tarbur Formation of Mandegan (a, c) and Naghan sections (b, d, f); oblique, partly tangential sections. e development of annular chambers (in grey) in some orbitolinids (modified from Douglass, 1960, fig. 21) and two sections (X–X' and Y–Y') comparable to those illustrated in a–d, and f. Abbreviations: b = beam, ch = chamber, ib = intercalary beam, s = septum, sn = subepidermal network. Thin-sections: Rt 63 (a), 2NG 183 (b), Rt 36 (c), 2NG 146 (d), 2NG 169 (f).
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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.