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Fig. 5 in Clarifying the identities of the Asian potamid genera Potamiscus Alcock, 1909, Ranguna Bott, 1966, and Dromothelphusa Naiyanetr, 1992 (Crustacea: Brachyura: Potamoidea)
Fig. 5. Ranguna rangoonensis (Rathbun, 1904), holotype male (65.0 × 49.8 mm) (MCZ 5562), Burma. A, dorsal view of carapace; B, frontal view of cephalothorax; C, epistome and antennules; D, right third maxilliped (outer view); E, left third maxilliped (deformed, outer view); F, left third maxilliped (deformed, inner view); G, right third maxilliped (inner view); H, left chela (outer view); I, right chela (outer view); J–M, left first to fourth ambulatory legs, respectively. Photographs courtesy of MCZ. Scales: A–C, H, I = 10.0 mm; D–G = 5.0 mm; J–M = 2.0 mm.
Fig. 1. Potamiscus annandalii Alcock, 1909 in Clarifying the identities of the Asian potamid genera Potamiscus Alcock, 1909, Ranguna Bott, 1966, and Dromothelphusa Naiyanetr, 1992 (Crustacea: Brachyura: Potamoidea)
Fig. 1. Potamiscus annandalii Alcock, 1909, lectotype male (33.0 × 25.0 mm) (ZSIK 6602-3/9), India. A, overall dorsal view; B, frontal view of cephalothorax; C, thoracic sternum, pleonal somites 4–6 and telson; D, sternopleonal cavity showing left G1 in situ; E, right G1 (ventral view); F, right G1 (dorsal view); G, right G2.
Fig. 3. Potamiscus annandalii Alcock, 1909. A–E in Clarifying the identities of the Asian potamid genera Potamiscus Alcock, 1909, Ranguna Bott, 1966, and Dromothelphusa Naiyanetr, 1992 (Crustacea: Brachyura: Potamoidea)
Fig. 3. Potamiscus annandalii Alcock, 1909. A–E, paralectotype male (30.5 × 25.7 mm) (NHM 1909.9.2.5), India; F, paralectotype female (30.0 × 23.1 mm) (NHM 1909.9.2.5), India. A, chelae (outer view); B, pleon and telson; C, left G1 (ventral view); D, left G2; E, sternopleonal cavity showing pleonal press-button locking mechanism; F, sternopleonal cavity showing vulvae.
Fig. 5 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 5. Rivellia maculipennis (holotype ♂ of Cephalia maculipennis Bigot, 1886) (Platystomatidae), UMO (photos by V. Korneyev, 2006): a — specimen, with labels; b — habitus dorso-laterally.
Fig. 8 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 8. Cephalia, non-type ♂ (a) and ♀ (b–f) from Har Hermon (photos by V. Korneyev, 2012): a — habitus right; b — same, left; c — head, left; d — thorax, left; e — same, dorsally; f — wing.
Fig. 2 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 2. Setellia femoralis (holotype ♂ of Cephalia femoralis Wiedemann, 1830) (Richardiidae), ZMUK (photos by V. Korneyev, 2008): a — habitus dorsally; b — labels; c — head, left; d — head, dorsally; e — thorax and abdomen, left; f — abdomen, dorsally; g — wing.
Fig. 1 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 1. Setellia fascipennis (holotype ♂ of Cephalia fascipennis Wiedemann, 1830) (Richardiidae), ZMUK (photos by V. Korneyev, 2008): a — habitus dorsally; b — labels; c — head and thorax, left; d — same, dorsally; e — abdomen, dorsally; f — wing; g — abdomen, mid and hind legs, left.
Fig. 4 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 4. Acrosticta fulvicornis (holotype ♀ of Cephalia fulvicornis Bigot, 1886) (Ulidiidae), UMO (photos by V. Korneyev, 2006): a — specimen, with labels; b — habitus dorso-laterally; c — head, dorsally; d — same, left.
Fig. 7 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 7. Cephalia rufipes (possible holotype ♀ of Cephalia nigripes Meigen, 1826) (Ulidiidae), MNHNP (photos by V. Korneyev, 2005): a — habitus dorsally and labels; b — same, postero-dorsally.
Fig. 3 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 3. Herina flavoscutellata (holotype ♀ of Cephalia flavoscutellata Becker, 1900) (Ulidiidae), ZMH http:// id.luomus.fi/GV.8191 (photos by P. Malinen, 2022, CC BY 4.0, partly modified): a — habitus dorsally; b — same, left; c — labels; d — head, left; d — arista; f — wing.
Fig. 6 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 6. Myrmecothea myrmecoides (holotype ♂ of Cephalia myrmecoides Loew, 1860) (Ulidiidae), MCZ (photos by V. Korneyev, 2001): a — habitus right view; b — labels; c — head; d, e — left and right wing, respectively.
Fig. 9 in Identity Of Species Assigned To The Genus Cephalia (Diptera, Tephritoidea)
Fig. 9. Cephalia, non-type ♂, NHMW (photos by V. Korneyev, 2017): a — epandrium, postero-ventrally; b — hypandrium, ventrally; c — ejaculatory apodeme; d — phallus, detached.
Operating diagram of IF incubator, two identical incubators were used for eggs that were already sorted. They are made up of an isothermal enclosure and contain three tiers (100 × 60 × 17 cm). The water circulating in each tier comes from the same filtration, cooling and sterilisation device. As a result, the eggs placed in the different tiers are subject to the same temperature regime. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of IF incubator, two identical incubators were used for eggs that were already sorted. They are made up of an isothermal enclosure and contain three tiers (100 × 60 × 17 cm). The water circulating in each tier comes from the same filtration, cooling and sterilisation device. As a result, the eggs placed in the different tiers are subject to the same temperature regime.
Top view of DR1/DR2 double riffle, each section contains a spawning ground made up of eight gravel-filled trays, a rest area. The "double riffle" was designed to accommodate two groups from 25 to 50 specimens of broodstock in strictly identical conditions. The spawning grounds are equipped with waterproof, motion-sensing cameras with infrared night vision, connected to a 1000 Gb recorder. The diurnal and nocturnal activities of the two groups can therefore be simultaneously recorded over a long period. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Top view of DR1/DR2 double riffle, each section contains a spawning ground made up of eight gravel-filled trays, a rest area. The "double riffle" was designed to accommodate two groups from 25 to 50 specimens of broodstock in strictly identical conditions. The spawning grounds are equipped with waterproof, motion-sensing cameras with infrared night vision, connected to a 1000 Gb recorder. The diurnal and nocturnal activities of the two groups can therefore be simultaneously recorded over a long period.
FIGURE 4 in Confirming the identity of the Hypogeococcus species (Hemiptera: Pseudococcidae) associated with Harrisia martinii (Labour.) Britton (Cactaceae) in Australia: implications for biological control
FIGURE 4 Mean (± SE) development time in days of the first- and second-generation females, from the first nymph to adult emergence of the Australian Hypogeococcus (W = 39, p = 0.0545).
FIGURE 3 in Confirming the identity of the Hypogeococcus species (Hemiptera: Pseudococcidae) associated with Harrisia martinii (Labour.) Britton (Cactaceae) in Australia: implications for biological control
FIGURE 3 Phylogenetic trees based on COI sequence data (a) maximum likelihood (IQ-TREE) and (b) Bayesian (Mr. Bayes). Branch labels indicate the ultrafast bootstrap and SH-aLRT values for the maximum likelihood tree and posterior probabilities for the Bayesian tree. Paracoccus marginatus was used as the outgroup for both trees. The host plant family is followed by the country of collection. See Table S1 for further details on host plant species and specimen collection codes for Hypogeococcus. **Country of collection includes Argentina, Brazil, Puerto Rico, and the United States.
FIGURE 2 in Confirming the identity of the Hypogeococcus species (Hemiptera: Pseudococcidae) associated with Harrisia martinii (Labour.) Britton (Cactaceae) in Australia: implications for biological control
FIGURE 2 Phylogenetic trees based on EF1α sequence data (a) maximum likelihood (IQ-TREE) and (b) Bayesian (Mr. Bayes). Branch labels indicate the ultrafast bootstrap and SH-aLRT values for the maximum likelihood tree and posterior probabilities for the Bayesian tree. Planococcus ficus was used as the outgroup for both trees. The host plant family is followed by the country of collection. See Table S1 for further details on host plant species and specimen collection codes for Hypogeococcus.
FIGURE 5 in Confirming the identity of the Hypogeococcus species (Hemiptera: Pseudococcidae) associated with Harrisia martinii (Labour.) Britton (Cactaceae) in Australia: implications for biological control
FIGURE 5 (a) Mean (± SE) pre-oviposition period (days) of the first virgin females, the second virgin, and second mated female generations (H = 19.491, p <0.0001), means labelled with similar letters are not significantly different (Dunn's test, p <0.05); (b) realised fecundity of the first virgin females, the second virgin and second mated female generations (H = 1.2429, p = 0.5372).
FIGURE 1 in Confirming the identity of the Hypogeococcus species (Hemiptera: Pseudococcidae) associated with Harrisia martinii (Labour.) Britton (Cactaceae) in Australia: implications for biological control
FIGURE 1 The different morphological features of the Australian Hypogeococcus: Panels (a) and (b) show that the abdominal region has three circuli (1–3); panel (c) shows that the head region has two antennae (4), numerous slender capitate setae (5), and numerous multilocular pores (6); panel (d) shows the presence of numerous slender capitate setae (5) and numerous multilocular pores (6) in the abdominal region; panels (e) and (f) show that the posterior ventral area possess numerous multilocular pores (6) and numerous conical setae (7); panels (g) and (h) show the foreleg (8) with the curvature attachment point, mid-leg (9) and hindleg (10), both with attachment points ending in a bifurcation. These characters are consistent with Hypogeococcus pungens s.s.
FIGURE 2 in Achieving kinematic identity across shape diversity in musculoskeletal modeling
FIGURE 2. The top images show an overlay of the reduced-asymmetry australopithecine pelvis (beige) with the ADL australopithecine pelvis (dark green). The bottom color-coded distance map pelvis show the distance between the reduced-asymmetry australopithecine pelvis with the ADL australopithecine pelvis.
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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.