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461,131 results for “FIGURES”
Figure 3. Cacopsylla hyalinonemae Li in Chinese psyllids in the genus Cacopsylla (Hemiptera: Sternorrhyncha: Psylloidea) associated with Spiraea (Rosaceae)
Figure 3. Cacopsylla hyalinonemae Li and Yang, 1989, adult. (a) Head, front view, antennae removed; (b) male terminalia, in profile, ignoring distal segment of aedeagus and phallobase; (c) inner view of paramere; (d) distal segment of aedeagus; (e) female terminalia, in profile; (f) fore wing; (g) hind wing; (h) distal two segments of antenna. Scale bar: a = 0.286 mm; b = 0.155 mm; c, d, h = 0.124 mm; e = 0.167 mm; f, g = 0.714 mm.
Figure 1 in Chinese psyllids in the genus Cacopsylla (Hemiptera: Sternorrhyncha: Psylloidea) associated with Spiraea (Rosaceae)
Figure 1. Cacopsylla falcata sp. nov., adult. (a) Head, front view, antennae removed; (b) male terminalia, in profile, ignoring distal segment of aedeagus and phallobase; (c) inner view of paramere; (d) distal segment of aedeagus; (e) female terminalia, in profile; (f) fore wing; (g) distal two segments of antenna. Scale bar: a = 0.25 mm; b, e = 0.155 mm; c, d, g = 0.124 mm; f = 0.625 mm.
Figure 5 in Morphology of tube-like threads related to Limnochares aquatica (L., 1758) (Acariformes: Hydrachnidia: Limnocharidae) in the laboratory
Figure 5. Scanning electron microscopy (SEM) of threads from the thread cloth and some external characteristics of the water mites Limnochares aquatica (L.). (a) Bunch of the hollow collapsed threads sometimes bending at different angles (arrow). Scale bar = 10 µm; (b) threads crossing freely and sometimes torn (arrow). Note a thread partly retaining its natural shape (arrowhead). Scale bar = 5 µm; (c) front view of a mite. Scale bar = 500 µm; (d) portion of the dorsal surface showing proposed dermal gland orifices (glandularia) provided either with a sensitive hair (arrows) or with a short spine (arrowheads). Scale bar = 100 µm; (e) slit-like orifice (arrow) provided with a sharp spine at the pole of the structure. Scale bar = 20 µm; (f) identical slit-like orifice (arrow) possessing a sensitive hair situated on the pedestal at the pole of the orifice. Scale bar = 20 µm.
Figure 2 in First record of a non-pollinating fig wasp (Hymenoptera: Sycophaginae) from Dominican amber, with estimation of the size of its host figs
Figure 2. Linear regression between Idarnes carme sp. gp ovipositor sheath lengths and median host fig diameters. Lines represent fitted model (red) and fig diameter ±95% CI (blue) for a 1.2 mm ovipositor sheath length, which represents the ovipositor sheath length of I. thanatos sp. nov. Each point represents a different fig wasp species and the fig diameter of its host species.
Figure 1 in Morphology of tube-like threads related to Limnochares aquatica (L., 1758) (Acariformes: Hydrachnidia: Limnocharidae) in the laboratory
Figure 1. Water mites Limnochares aquatica (L.) and threads' associations during maintenance in the laboratory. (a) A mite in a drop of water with white spots on the dorsal surface (arrows); (b) Another, larger, mite in a drop of water revealing a small white flock on the posterior portion of the idiosoma (arrow); (c) A mite engaging with an extremely large flock association at its venter (arrowhead). Note the hardly distinguished possible detachment of the colourless threads from the dorsal body surface (arrow) forming figures of balls; (d) The balls of threads containing also inclusions of additional organic substances. Scale bars = 1 mm.
Figure 7 in Improving knowledge of the cyclorrhaphan larva (Diptera)
Figure 7. Coelopa frigida (Coleophidae), third stage preserved larva, lateral view, head to the right, from the 2nd abdominal segment to the pseudocephalon, showing distribution of black spicules, length 5 mm.
Figure 5 in Improving knowledge of the cyclorrhaphan larva (Diptera)
Figure 5. Cibarial ridges and head skeleton pump in the basal sclerites of cyclorrhaphan larvae, mandibles to the left. a, head skeleton in situ, third stage larva of Alipumilio femoratus Shannon (Diptera, Syrphidae), ventro-lateral view, 1 = mandibles, 2 = cibarial ridges on the floor of the basal sclerite; b, Eumerus sp. Meigen (Syrphidae), lateral view, 3 = pharynx running along the floor of the basal sclerite, 4 = valve at the rear of the upturned ventral cornu, 5 = bands of muscle originating on the dorsal cornu and inserting on the roof of the pharynx and the ventral cornu that operate the pump, specimen prepared and donated by C.J. Hartley to the National Museums, Scotland.
Figure 4 in Improving knowledge of the cyclorrhaphan larva (Diptera)
Figure 4. Head skeletons of exemplar saprophages, lateral view, mandible towards centre; figures in parentheses are lengths of the basal sclerites in mm. a, Neophyllomyza acyglossa (Milichiidae) (0.2); b, Leucophora personata (Collin) (Anthomyiidae) (0.4); c, Chyromya femorellum (Fallén) (Chyromyidae) (0.4); d, Strongylophthalmyia ustulata (Zetterstedt) (Strongylophthalmyiidae) (0.4); e, Lonchaea nitens (Lonchaeidae) (0.3); f, Meoneura lamellata Collin (Carnidae) (0.2); g, Stegana coleoptrata (Drosophilidae) (0.4); h, Camilla fuscipes Collin (Camillidae) (0.3); i, Suillia variegata (Loew) (Heleomyzidae) (0.5); j, Lonchaea sylvatica (Lonchaeidae) (0.3).
Figure 2 in Morphology of tube-like threads related to Limnochares aquatica (L., 1758) (Acariformes: Hydrachnidia: Limnocharidae) in the laboratory
Figure 2. Threads of the water mites Limnochares aquatica (L.) in a light microscope. (a) Freely interlaced threads in oil immersion in a common microscope. Note that practically colourless threads are unbranched and totally devoid of any internal substances, being sometimes bent at different angle. Scale bar = 20 µm; (b) Differential-interferential contrast (DIC) showing threads' replicas. Scale bar = 5 µm; (c) DIC of gentian-violet stained preparation showing both empty threads and thread with a core (arrow). Scale bar = 20 µm; (d) Bright field (BF) of gentian-violet stained preparation obviously indicating colourless threads and contaminating bacteria and bacterial chain (arrows) freely dispersed in the sample. Scale bar = 5 µm.
Figure 8 in Chinese psyllids in the genus Cacopsylla (Hemiptera: Sternorrhyncha: Psylloidea) associated with Spiraea (Rosaceae)
Figure 8. Microscopic photograph of fore wing membrane of Cacopsylla spp., showing texture of surface spinules. (a) C. falcata sp. nov.; (b) C. hyalinonemae Li and Yang, 1989; (c) C. nocturna sp. nov.; (d) C. qilianensis sp. nov.; (e) C. spiraeicola (Li, 2011).
Figure 5 in The type specimens and type localities of the orangutans, genus Pongo Lacépède, 1799 (Primates: Hominidae)
Figure 5. The nomenclature and geographic distribution of the subspecies of Pongo pygmaeus, (A) following Groves (2001), and (B) as revised in this paper
Figure 6 in Sharing the space: coexistence among terrestrial predators in Neotropical caves
Figure 6. Ordering diagram for the five model species produced by the canonical correspondence analysis (CCA). Legend: Hum = humidity; Temp = temperature; Subs = substrate.
Figure 2 in Swimming and bipedal bottom-running in the pig-nosed turtle Carettochelys insculpta Ramsay, 1886
Figure 2. Detail of hindlimb action during bipedal bottom running in large Carettochelys insculpta. Numerals indicate field sequence. Tail is stippled. Short horizontal lines indicate substratum beneath hindlimbs. Note that, at field 6, neither rear limb is in contact with the substratum.
Figure 2 in Sharing the space: coexistence among terrestrial predators in Neotropical caves
Figure 2. Substrate categories utilised for the field observations and the canonical correspondence analysis (CCA). Rocky substrates: (a) wall and (b) unconsolidated substrate (scale = 5 cm). Organic substrates: (c) guano (forceps for scale) and (d) leaf litter. Photographs by the authors.
Figure 1 in Terrestrial isopods and myriapods in a forested scree slope: subterranean biodiversity, depth gradient and annual dynamics
Figure 1. Distribution of Isopoda, Diplopoda and Chilopoda along the depth gradient of the scree slope expressed as the total number of individuals trapped in two sampling periods (November 2008–November 2009; November 2009–July 2010).
Figure 5 in Sharing the space: coexistence among terrestrial predators in Neotropical caves
Figure 5. Ordering diagram of the species produced by the canonical correspondence analysis (CCA). Legend: Hum = humidity; Temp = temperature; Subs = substrate. The codes for species are given in Appendix 1.
Figure 2 in Observations of multiple pelagic egg masses from small-sized jumbo squid (Dosidicus gigas) in the Gulf of California
Figure 2. (a) Distribution of ommastrephid egg mass diameters. Dosidicus gigas (small) are from the present study. Dosidicus gigas (large) is from Staaf et al. (2008). Illex illecebrosus are from Durward et al. (1980) and O'Dor and Balch (1985). Nototodarus gouldi are from O'Shea et al. (2004). Todarodes pacificus are from Bower and Sakurai (1996) and Puneeta et al. (2015). (b) 80-cm egg mass (30 May #1). (c) 122-cm egg mass (29 May #2).
Figure 31 in Rocky-intertidal cheilostome bryozoans from the vicinity of the Sesoko Biological Station, west-central Okinawa, Japan
Figure 31. Bryopesanser latesco Tilbrook: (a) NSMT-Te 1167, autozooids; (b) NSMT-Te 1100, orifice; (c) NSMT-Te 1054, ovicelled and non-ovicelled autozooids; (d) NSMT-Te 1103, ovicelled and nonovicelled autozooids; note sharp projection on proximal peristomial rim in lower-right zooid, and size difference in avicularia between lower right and lower left zooids. Panels are scanning electron microscopic images of dried, unbleached specimen (a) or bleached specimens (b–d). Scale bars: a, c, d = 300 µm; b = 100 µm.
Figure 37 in Rocky-intertidal cheilostome bryozoans from the vicinity of the Sesoko Biological Station, west-central Okinawa, Japan
Figure 37. Rhynchozoon lunifrons sp. nov.: (a) NSMT-Te 1196 (paratype), colony view; (b) enlargement from preceding panel, showing autozooids typically having three processes associated with orifice; (c–f) NSMT-Te 1197 (paratype), (c) marginal autozooids showing shape and orientation of suboral avicularian chamber, (d) marginal autozooids, showing orifice shape, (e) well-calcified ovicelled autozooids, showing large semicircular area of exposed entooecium on ovicell, (f) endozooidal ovicells, with three zooids showing a second ovicell (arrowheads) lateral to orifice. All panels are scanning electron microscopic images of bleached specimens. Scale bars: a = 1.0 mm; b = 500 µm; c–f = 300 µm.
Figure 29 in Rocky-intertidal cheilostome bryozoans from the vicinity of the Sesoko Biological Station, west-central Okinawa, Japan
Figure 29. Arthropoma harmelini sp. nov., NSMT-Te 1159 (holotype): (a) autozooids, showing crescentic suboral umbo, which in top-centre zooid is continuous with peristomial rim; (b) orifice; (c) ovicelled autozooids, with one ovicell showing a lateral extension; note there is no row of pseudopores between orifice and floor of developing ooecium; (d) ovicelled and non-ovicelled autozooids; (e) autozooids with developing ooecia; note lack of pseudopores between orifice and floor of ooecium; (f) colony margin, showing interzooidal connections. All panels are scanning electron microscopic images of bleached specimen. Scale bars: a, c, e, f = 300 µm; b = 100 µm; d = 500 µm.
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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.