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Fig. 77–87 in Review Of The Genus Geloemyia (Diptera, Pyrgotidae), With Discussion Of Its Taxonomic Position
Fig. 77–87. Geloemyia stylata: holotype ♀ (NHMW): 77 — habitus; 78 — head, anterolateral view; 79 — antennae, lateral view; 80 — right wing, ventrally; 81 — left wing, ventrally; 82 — postgena, proepisternum and fore femur, posterior view; 83 — mid femur, anterior view; 84 — hind femur, anterior view; 85 — scutellum; 86 — abdomen, lateral view; 87 — labels.
Fig. 62–66 in Review Of The Genus Geloemyia (Diptera, Pyrgotidae), With Discussion Of Its Taxonomic Position
Fig. 62–66. Geloemyia namibica, sp. n., paratype ♂ (62–64) (MNKB) and ♀ (65–66) (SIZK): 62 — abdomen, ventral view; 63 — epandrium, lateral view; 64 — glans of phallus; 65 — aculeus; 66 — spermatheca (one of the three).
Fig. 54–61 in Review Of The Genus Geloemyia (Diptera, Pyrgotidae), With Discussion Of Its Taxonomic Position
Fig. 54–61. Geloemyia namibica, sp. n., paratype ♀ (SIZK): 54 — habitus; 55–58 — head (55 — lateral, 56 — anterolateral, 57 — dorsal, 58 — anteroventral view); 59 — wing; 60 — mesonotum, dorsal view; 61 — labels.
Fig. 1–10 in Review Of The Genus Geloemyia (Diptera, Pyrgotidae), With Discussion Of Its Taxonomic Position
Fig. 1–10. Geloemyia wings: 1 — G. namibica Korneyev, sp. n.; 2 — G. wonjuensis; 3–4 — G. trifasciata (3 — ♀, 4 — ♂); 5 — G. cockerelli; 6 — G. trifasciata holotype ♀; 7 — G. cheni Kim, Han & Korneyev, sp. n. paratype ♀; 8–9 — G. quadriseta (8 — syntype ♀ G. quadriseta, syntype ♀ G. ornata); 10 — G. nigrofasciata holotype ♀; dm — discomedial cel; cua — anterior cubital cell; dm-cu — discal mediocubital crossvein; cua — anterior cubital cell; arrows indicate spurious vein.
Fig. 16–20 in Taxonomic Review Of The Genus Yunnantettix (Orthoptera, Tetrigidae) From The Oriental Region
Fig. 16–20. Yunnantettix bannanensis, male (16–17) and Y. elytratus, female (18–20): 16, 18 — head and pronotum, lateral view; 17 — body, dorsal view; 19 — head and pronotum, dorsal view; 20 — head, frontal view (16–17 after Zheng, 1995; 18–19 after Günther, 1939, with modification; 20 after Shishodia, 1991).
Fig. 1–13 in Taxonomic Review Of The Genus Yunnantettix (Orthoptera, Tetrigidae) From The Oriental Region
Fig. 1–13. Yunnantettix thaicus sp. n.: 1 — male head and pronotum, lateral view; 2 — female anterior part of pronotum, lateral view; 3 — male head and anterior part of pronotum, dorsal view; 4 — male head, frontal view; 5 — female antenna, dorsal view; 6 — male hind femur, lateral view; 7 — male fore femur, lateral view; 8 — male hind tarsus, lateral view; 9 — male apex of abdomen, lateral view; 10 — the same, dorsal view; 11 — the same, ventral view; 12 — female apex of abdomen, lateral view; 13 — female 7th sternite and subgenital plate, ventral view. Scale bars 1 mm.
Fig. 1 in A Review Of Major Impact Factors Of Hostilities Influencing Biodiversity In The Eastern Ukraine (Modeled On Selected Animal Species)
Fig. 1. Spatial distribution of ignitions in 2010–2014 on studied area (dotted line is ATO zone's limits in 1.06– 30.09.2014).
Fig. 5 in A Review Of Major Impact Factors Of Hostilities Influencing Biodiversity In The Eastern Ukraine (Modeled On Selected Animal Species)
Fig. 5. Distribution of two snake species, H. caspius and E. dione, in Ukrainian East (ATO zone is indicated by dotted line, burnt area marked inside zone).
Fig. 3 in A Review Of Major Impact Factors Of Hostilities Influencing Biodiversity In The Eastern Ukraine (Modeled On Selected Animal Species)
Fig. 3. Spatial local distribution of ignitions in 2010–2014 in the outskirts of Slavyanoserbsk, Luhansk Region.
APPENDIX A - SEARCH PROTOCOLE AND PAPERS LIST - Cognitive Neuroscience's Transposition in STEAM Classroom: A Systematic Literature Review
<p>An integrative literature review was performed corresponding to PRISMA’ protocol in order to integrate issues over an innovative curriculum through cognitive sciences didactic transposition in STEAM classrooms. The search action was handled using various international databases. Each paper was selected alongside the PICO strategy and a defined selection criterion. Analysis of the literature between 2000 and 2021 is presented.</p>
Fig. 88–99 in Review Of The Genus Geloemyia (Diptera, Pyrgotidae), With Discussion Of Its Taxonomic Position
Fig. 88–99. Geloemyia trifasciata: non-type ♀ (88, 90–96) and ♂ (89, 97–99) (SIZK): 88, 89 — habitus, left; 90, 91 — head (90 — lateral, 91 — anterior view); 92 — right wing, dorsally; 93 — apex of oviscape and eversible membrane, lateral view; 94 — aculeus, ventrally; 95 — same, apex, enlarged; 96 — spermathecae; 97 — epandrium and hypandrium, right view; 98, 99 — phallus glans (98 — ventral, 99 — lateral view).
FIG. 1 in What, if anything, is Lycosa accentuata Latreille, 1817? - Review of a nomenclatural conundrum (Araneae: Lycosidae)
FIG. 1. — Schematic timeline of the different interpretations of Latreille's Lycosa accentuata Latreille, 1817. The names on the right are the most closely matching currently valid taxa, and the years refer to the major taxonomic publications detailed and discussed in Table 1. It is clear that the recent inversion of preceding usage, as proposed by Canard & Cruveillier (2019), contradicts all previous interpretations of the name. This figure should be read in conjunction with the detailed information in Table 1.
FIG. 2 in What, if anything, is Lycosa accentuata Latreille, 1817? - Review of a nomenclatural conundrum (Araneae: Lycosidae)
FIG. 2. — Neotype of Lycosa accentuata Latreille, 1817 (junior subjective synonym of Araneus trabalis Clerck, 1757) from forêt de Fontainebleau near Paris: A, dorsal view; B, ventral view; C, epigyne in situ. Scale bars: A, B, 5 mm; C, 0.2 mm.
Fig. 6 in A review of the Asian species of the Cercyon unipunctatus group (Coleoptera: Hydrophilidae: Sphaeridiinae)
Fig. 6. Cercyon undulipennis sp. nov. A – dorsal and lateral habitus of paratype from China: Yunnan: Gaoligong Shan; B–D – male genitalia of the holotype (B – tegmen; C – median lobe; D – sternite 9). E–H – ventral morphology (E – meso- and metaventrite; F – detail of mesoventral plate; G – mentum; H – prosternum and antennal groove).
fig. 6 in Review of the Late Jurassic erymoid lobsters (Crustacea: Decapoda)
fig. 6) of Eryma fossata (Oxfordian, Galgenberg near Hildesheim, Germany); J, original figure of Sauvage (1891: pl. 4, fig. 6) of Eryma leblanci (Kimmeridgian, Boulogne-sur-Mer, France); K, original figure of Sauvage (1891: pl. 3, fig. 5) of Eryma boloniensis (Kimmeridgian, Boulogne-sur-Mer, France); L, original figure of Sauvage (1891: pl. 4, fig. 3) of Eryma beaugrandi (Kimmeridgian, Boulogne-sur-Mer, France); M, N, original figures of Morière (1883: pl. 1, figs 1-2) of the syntypes of Eryma villersi (Oxfordian, Villers-sur-Mer, France); O, original figure of Van Straelen (1925: pl. 9, fig. 1) of the holotype of Eryma morieri Hée, 1924 (Oxfordian, Villers-sur-Mer, France); P, Q, specimen from the Callovian of Villers-sur-Mer (France, private collection of J.-P. Pezy). Photographs: L. Cazes. Scale bars: 1 cm.
RICE WHEAT CROPPING SYSTEMS-CONSTRAINTS AND STRATEGIES : A REVIEW
<p>The rice-wheat cropping system (RWCS) in the Indo-Gangetic plains (IGP) of South Asia with the help of Green<br> Revolution in the early 1970’s greatly contributed to India's food self-sufficiency and livelihood of millions of<br> peoplethus, became the country's primary source of food-grain production. However, deterioration of soil health and<br> quality, ground water depletion, water stress, labour shortage, introduction of new weeds and pests particularly<br> Phalaris minor, Scirpophaga incertulas and climate change have all contributed to a major production standstill and<br> deterioration in recent years by which the sustainability of rice wheat cropping system is now at jeopardy. Traditional<br> agronomic practices had various negative implications on the sustainability of rice wheat cropping system with the<br> introduction of HYVs. So, a paradigm shift is required to achieve long-term productivity, sustainability and allow<br> farmers to minimise inputs, optimise yields, enhance profitability, maintain the natural resource base and reduce risk<br> owing to both environmental and economic issues through resource-conserving technologies (RCTs) including<br> zero/minimaltillage, PUSA decomposer, bed planting, crop residue management, mechanical rice transplanter (MRT)<br> and crop diversification. This article focuses some of the issues that need to be addressed in the RWCS in order to<br> achieve the goal of increasing regional productivity and assuring food security while maximising the effective use of<br> natural resources, enhancing rural livelihoods and aiding in poverty alleviation.</p>
Figure 98 in A review of the genus Leiurus Ehrenberg, 1828 (Scorpiones: Buthidae) with description of four new species from the Arabian Peninsula
Figure 98: Selected morphometrics of Leiurus, Cicileiurus, Cicileus and Compsobuthus compared to other Buthus group scorpions. A–B. Scatter plots of the fraction of fixed finger length distal to db (A) and est (B) vs. the ratio of movable finger length to carapace length. Each point represents one sex of one species. Larger ordinate values correspond to more basal positions of the trichobothria, and larger abscissa values to longer pedipalp fingers. There was a significant inverse correlation between relative length of the portion of the fixed finger distal to db and est (R = -0.6534, -0.5488, respectively), and the relative length of the movable finger (the latter being a measure of elongation of both fixed and movable fingers). Highlighted symbols show that Leiurus (light magenta circles), Cicileiurus (red triangle), Cicileus (green squares) and Compsobuthus (yellow circles) are located in the lower right halves of the plots, i.e. all have relatively elongated fingers and more distal placement of both db and est. Gray circles are data from other Buthus group species. C. Scatter plot of the fraction of fixed finger length distal to db vs. the fraction distal to est. The strong positive correlation (R = 0.8052) indicates a tendency for db and est to move together towards more distal locations as the fixed finger becomes more elongated. Species above the diagonal (solid blue) have db proximal to est, and those below have db distal to est. Solid gray lines in A–C are fits by least squares regression through all points. D. Scatter plot of pedipalp femur L/W (a measure of pedipalp elongation) vs. carapace L (a measure of body size). These two variables were not significantly correlated (R = 0.094). Data were compiled from the literature and specimens in the authors collections for 38 genera and 203 species representing the majority of taxa in the Buthus group, including both males (N = 124) and females (N = 97). Genera (and number of species) included: Afghanobuthus (1), Androctonus (11), Apistobuthus (2), Baloorthochirus (1), Birulatus (2), Buthacus (13), Butheoloides (11), Butheolus (5), Buthiscus (1), Buthus (26), Cicileiurus (1), Cicileus (2), Compsobuthus (33), Congobuthus (1), Darchenia (1), Gint (1), Hemibuthus (1), Hottentotta (31), Leiurus (10), Liobuthus (1), Lissothus (3), Mesobuthus (7), Neobuthus (2), Odontobuthus (6), Orthochirus (12), Pantobuthus (1), Pectinibuthus (1), Plesiobuthus (1), Polisius (1), Razianus (3), Saharobuthus (1), Somalibuthus (1), Vachoniolus (4), Vachonus (1).
Figure 100 in A review of the genus Leiurus Ehrenberg, 1828 (Scorpiones: Buthidae) with description of four new species from the Arabian Peninsula
Figure 100: Geographic plot of locality data of material examined for five species of Leiurus from the Arabian Peninsula. Map colored by terrain with shaded relief, indicating major physiographic regions.
Figure 96 in A review of the genus Leiurus Ehrenberg, 1828 (Scorpiones: Buthidae) with description of four new species from the Arabian Peninsula
Figure 96: Carapace and tergites I–III of representatives of six genera of the Buthus group. A. Compsobuthus acutecarinatus (Simon, 1882), male, Jabal Qara, Oman. B. Cicileus exilis (Pallary, 1928), male, Hoggar, Algeria. C. Leiurus quinquestriatus (Ehrenberg, 1828), female, Egypt. D. Sassanidotus gracilis (Birula, 1900), female, Hormozgan Prov., Iran. E. Odontobuthus bidentatus Lourenço & Pézier, 2002, male, Omidiyeh, Iran. F. Apistobuthus susanae Lourenço 1998, male, Albadji, Iran. Scale bars: A, B, D: 1 mm; C, E, F: 2 mm.
Figure 93 in A review of the genus Leiurus Ehrenberg, 1828 (Scorpiones: Buthidae) with description of four new species from the Arabian Peninsula
Figure 93: Medial intercarinal areas of tergite III of female Leiurus spp. A. L. arabicus sp. n., paratype, Jeddah, Saudi Arabia. B. L. arabicus sp. n., paratype, Wadi Khumrah, Saudi Arabia (NHMB 17bj). C. L. haenggii sp. n., paratype, Yemen. D. L. haenggii sp. n., paratype, Wadi Maraba, Saudi Arabia (NHMB 17al). E. L. heberti sp. n., paratype, Jabal Samhan. Oman. F. L. abdullahbayrami Yağmur, Koç et Kunt, 2009, Caybasi Village, Turkey. G. L. brachycentrus (Ehrenberg, 1829) stat. n., Al Mansuriah, Yemen. H. L. macroctenus sp. n., paratype, Masirah Island, Oman. I. L. hebraeus (Birula, 1908) stat. n., Israel (NHMB 17a). J. L. hebraeus Birula, 1908, Kurayyima, Jordan. K. L. quinquestriatus (Ehrenberg, 1828), Kharga Oasis, Egypt (NHMB 17i). L. L. jordanensis Lourenço, Modry et Amr, 2002, al-Tawil, Saudi Arabia.
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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.