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432 results for “morphological development”
Spatiotemporal Patterns of Gene Expression During Development of a Complex Colony Morphology
GEO Series GSE274952. Saccharomyces cerevisiae. 36 samples. Type: Expression profiling by high throughput sequencing.
SNP microarray based 24 chromosome aneuploidy screening demonstrates that cleavage stage FISH poorly predicts aneuploidy in embryos that develop to morphologically normal blastocysts
GEO Series GSE18932. Homo sapiens. 206 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
FIGURE 9 in Morphological development, distribution and ecology of the arctic oribatid mite Hermannia scabra (Acari: Oribatida: Hermanniidae) and synonymy of Hermannia gigantea
FIGURE 9. Hermannia scabra (L. Koch, 1879), adult, microscope images: A—notogaster, dorsal view; B—tubercles of notogaster at surface focus; C—the same as B, but at deep focus (tuberculate and porose surface visible).
FIGURE 18 in Morphological development, distribution and ecology of the arctic oribatid mite Hermannia scabra (Acari: Oribatida: Hermanniidae) and synonymy of Hermannia gigantea
FIGURE 18. Hermannia scabra (L. Koch, 1879), larva (A) and tritonymph (B, C), SEM micrographs: A—anterior view; B—dorsal view; C—part of reticulate prodorsal surface with bothridial and exobothridial setae and bothridium. Scale bars 50 μm (A), 100 μm (B), 20 μm (C).
FIGURE 2 in Morphological development, distribution and ecology of the arctic oribatid mite Hermannia scabra (Acari: Oribatida: Hermanniidae) and synonymy of Hermannia gigantea
FIGURE 2. Hermannia scabra (L. Koch, 1879), adult: A—ventral view (subcapitulum and legs omitted); B—acetabula I–III, basal part of prodorsum and anterior part of notogaster, lateral view; C—posterior part of body, lateral view. Scale bar 100 μm.
FIGURE 1 in The parasitic barnacle Peltogaster reticulata Shiino, 1943 (Rhizocephala, Peltogastridae) fromRussian watersof the Sea of Japan:morphological description molecular identification and complete larval development
FIGURE 1. Pagurus minutus infested by Peltogaster reticulata, from Russian waters of the Sea of Japan (A), body outlines of the externa (B), immature externa (C); mature externae (D, E). Scale bar 1 mm.
Fig. 5 in Early development of Monoplex pilearis and Monoplex parthenopeus (Gastropoda: Cymatiidae): biology and morphology
Fig. 5 Comparison of the centroid sizes of M. parthenopeus and M. pilearis veliger lateral view images. The data shown are from the primary dataset. The centroid sizes of M. parthenopeus and M. pilearis were statistically significant according to two-sample normal Student's t test with a p value of <0.00001
Fig. 2 in Early development of Monoplex pilearis and Monoplex parthenopeus (Gastropoda: Cymatiidae): biology and morphology
Fig. 2 Egg clutches of M. pilearis and M. parthenopeus. a View from above and b view from the side of female M. pilearis with freshly laid egg clutch. c Female M. parthenopeus incubating egg clutch and d M. parthenopeus egg clutch after larvae have emerged from eggs and begun to form shells, approximately 12 days post-laying
Fig. 2 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)
Fig. 2 Flight and jumping musculatures of the bark louse genus Stenopsocus (Psocodea: BPsocoptera^: Stenopsocidae), lateral view. Redrawn and modified from Badonnel (1934) and Maki (1938). Indirect flight muscles were colored blue: DLM, dorsal longitudinal indirect flight muscle (dlm1); DVM, dorsoventral flight muscle (dvm1); ODM, oblique dorsal flight muscle (dlm2/3). Trochanter depressor muscles were colored by respective muscles. Terminology followed Crossley (1978), Brodsky (1994) and Beutel et al. (2014). The border of mesophragma is highlighted by green line
Fig. 4 in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 4 Young lateral shoots of P. vulgaris (material collected in June). Frontal views of plants with all but very young leaves removed. Phyllotaxy is anticlockwise in (a, c) and clockwise in (b, d). a A lateral shoot is formed in axil of the leaf i, then the main axis has formed flowers ii, iii (removed) and iv (probably abortive). b A lateral shoot is present in the axil of the leaf i, flower ii is removed, flower iii is very young. c A lateral shoot in the axil of the leaf i is formed, then the main axis has formed flowers ii (removed), iii, iv, v. d A lateral shoot in the axil of the leaf vi is formed, then the main axis has formed flowers vii, viii (removed), ix, x. Arabic figures 0 leaves of lateral shoots. Scale bars 0300 μm
Fig. 7 Pinguicula vulgaris, early flower development. a The earliest stage with a in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 7 Pinguicula vulgaris, early flower development. a The earliest stage with a very narrow calyx rim marked by arrows. b,c Initiation of calyx and androecium; the two massive stamen primordia appear just before corolla initiation. d-e Flowers with median abaxial petal initiated. f-i Further development of corolla. f and i Different views of the same flower, while g and h are different views of another flower. In f no connection between the median lower lip petal and lateral lower lip petals observable, but in i at the same young flower (as well as in another flower in g and h) it is clearly visible. h-i All petals are united by a rim. At this stage, the gynoecium is not visible. Abbreviations: pl, lower lip petals; pu, upper lip petals; s, spur, sl, lower lip sepals; su, upper lip sepals; st, stamen. Scale bars 0200 μm (a, b, c, f, g, h), 300 μm (d, e. i)
Fig. 2 in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 2 Shoot branching in Pinguicula alpina. Frontal view of shoot apices (a, d), their diagrams (b, e) and schematic representation of shoot systems (c, f). In a-c (collected 21 September 2006), leaves i-iii form a clockwise spiral, followed by flowers iv-vi; a lateral shoot with a clockwise spiral (prophylls 1-2 followed by flower 3) is present in the axil of leaf iii; leaves a-g form an anticlockwise spiral and belong to a shoot in the axil of the leaf 2. In d-f (collected 1 September 2006), leaves i-iv form an anticlockwise spiral followed by flower v; a lateral shoot with an anticlockwise spiral 1-5 is present in the axil of the leaf iv. Scale bars 0500 μm (a), 200 μm (d)
FIGURE 1 in Learning from Linnaeus: towards developing the foundation for a general structure concept for morphology*
FIGURE 1. Aristotelian definitions: The definition of the 'parent' kind is inherited by all of its 'first child generation' kinds and forms the Genus part of their definitions. These represent properties that an instance of a 'child' kind necessarily has to possess. On the other hand, the essential property of a 'child' kind represents the distinguishing property that is in combination with the Genus part sufficient for the recognition of an instance of that kind, since all and only individuals that are instances of this kind do possess this property. This forms the Differentia part of the kind's definition. Genus and Differentia together represent the essence of the kind and at the same time its definition.
FIGURE 4. Zoea VI in Larval development of the freshwater shrimp Atyaephyra desmarestii (Millet, 1831) sensu lato (Decapoda: Caridea: Atyidae) and morphological maturation from juveniles to adults
FIGURE 4. Zoea VI: A. Telson; B. Antennule; C. Antenna; D. Maxilla; E. 2nd Maxilliped; F. 3rd Maxilliped; G. 1st Pereiopod; H. 2nd Pereiopod. Scales: A. 2.35 mm; B. 1.57 mm; C. 3.33 mm; D. 2.74 mm; E. 0.49 mm; F. 1.27 mm; G. 1.76 mm; H. 1.86 mm.
Figure 8 in Postcranial skeletal development of Mugil cephalus (Teleostei: Mugiliformes): morphological and life-history implications for Mugiliformes
Figure 8. Drawings of development stages of the three anterior anal fin pterygiophores in Mugil cephalus larvae. A, L3: 3.9 mm standard length (SL), 15 days post-hatching (dph). B, L4: 4.6 mm SL, 19 dph. C, L6: 7.2 mm SL, 25 dph. Blue, cartilage; pink, bone. Abbreviations: dr, distal radial; pr, proximal radial. Scale bars: 100 µm.
Figure 4 in Postcranial skeletal development of Mugil cephalus (Teleostei: Mugiliformes): morphological and life-history implications for Mugiliformes
Figure 4. Detailed photographs of the anterior vertebral column of a cleared and stained specimen of Mugil cephalus (DMM IE/16314; L6: 6.5 mm standard length). A, dorsal view. B, dorsolateral view of the right side. Abbreviations: ec, epicentral; ep, epipleural; pa, parapophysis; ri, rib; vc, vertebral centrum. Scale bars: 200 µm.
Figure 6 in Postcranial skeletal development of Mugil cephalus (Teleostei: Mugiliformes): morphological and life-history implications for Mugiliformes
Figure 6. Drawings of development stages of the pectoral girdle in Mugil cephalus larvae. A, L1: 3.0 mm notochord length (NL), 14 days post-hatching (dph). B, L3: 3.6 mm NL, 18 dph. C, L4: 4.4 mm standard length (SL), 19 dph. D, L6: 7.2 mm SL, 25 dph. Blue, cartilage; pink, bone. Abbreviations: cl, cleithrum; co, coracoid; co-sc, coracoscapular cartilage; dr, distal radial; pcd, dorsal postcleithrum; pcv, ventral postcleithrum; pr, proximal radial; ptm, posttemporal; sc, scapula; su, supracleithrum. Scale bars: 200 µm.
FIGURE 4 in Morphology of developing larvae and a dichotomous key for five bubble-nesting Betta species (Teleostei: Osphronemidae)
FIGURE 4. Morphological and pigmentation features of immature stages of Betta imbellis (KUMF 7066). (a) Newly hatched larva (NL = 2.37 mm); (b) day 1 yolk sac larva (NL = 2.82 mm); (c) day 3 pre-flexion larva (NL = 2.98 mm); (d) day 9 preflexion larva (NL = 3.39 mm); (e) day 12 flexion larva (NL = 3.68 mm); (f) day 18 post-flexion larva (SL = 3.86 mm); (g) day 31 post-flexion larva (SL = 10.20 mm); (h) day 40 juvenile (SL = 12.88 mm).
FIGURE 6 in Morphology of developing larvae and a dichotomous key for five bubble-nesting Betta species (Teleostei: Osphronemidae)
FIGURE 6. Morphological and pigmentation features of immature stages of Betta siamorientalis (KUMF 7068); (a) Newly hatched larva (NL = 2.57 mm); (b) day 1 yolk sac larva (NL = 2.85 mm); (c) day 3 pre-flexion larva (NL = 3.12 mm); (d) day 9 pre-flexion larva (NL = 5.10 mm); (e) day 12 flexion larva (NL = 5.21 mm); (f) day 18 post-flexion larva (SL = 6.57 mm); (g) day 23 post-flexion larva (SL = 8.68.40 mm); (h) day 40 juvenile (SL = 11.56 mm).
FIGURE 2 in Morphology of developing larvae and a dichotomous key for five bubble-nesting Betta species (Teleostei: Osphronemidae)
FIGURE 2. General illustrations of Betta species' yolk sac larvae (A) and juvenile (B) showing morphometric characters and dark pigmentation patterns. Abbreviations of body dimensions: NL = notochord length, SL = standard length, BD = body depth, HL = head length, PreAL = pre-anal length, ED = eye diameter. Abbreviations for pigmentation patterns: a = punctate spot, b = stellate spot, c = longitudinal stripe along dorsal edge of yolk sac, d = faded stripe along ventral edge of tail, e = pre-orbital bar, f = first sub-orbital bar, g = second sub-orbital bar, h = post-orbital bar, I = post-orbital bar, j = pectoral fin base bar, k = dorsal stripe, l = central stripe, m = ventral stripe, n = caudal spot, o = small punctate spots on caudal fin.
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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.