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642 results for “ornaments”
Fig. 6 in Sexually dimorphic ornamentation in modern spinicaudatans and the taxonomic implications for fossil clam shrimps
Fig. 6. Carapaces and ornamentations of representatives of the extant spinicaudatan family Leptestheriidae. A. Leptestheria kawachiensis Uéno, 1927, from Hubei, China, NIGP Cr. 101, male, lateral view; left valve, oval outline (A1); growth bands in the upper part of carapace with wide radial fringes pattern (A2). B. Eoleptestheria ticinensis (Balsamo-Crivelli, 1859), from Jiangsu, China, NIGP Cr. 61, male, lateral view; right valve, oval outline (B1); growth bands in the ventral part of carapace with shallow fringes pattern, never developing reticulation or punctae between fringes (B2); details of ventral growth bands with shallow fringes pattern separated with smooth surface (B3, B4).
Fig. 4 in Sexually dimorphic ornamentation in modern spinicaudatans and the taxonomic implications for fossil clam shrimps
Fig. 4. Ornamentations on the growth bands in the extant spinicaudatan branchiopod Eulimnadia sp. and the extant laevicaudatan branchiopod Lynceus sp. A, B. Eulimnadia sp., from Jiangxi, China. A. NIGP Cr. 161, male, carapace in lateral view. B. NIGP Cr. 162, female, unornamented area near the ventral margin. C, D. Lynceus sp., from Heilongjiang, China. C. NIGP Cr. 173, male, carapace in lateral view. D. NIGP Cr. 174, female, isogonal reticulate ornamentation in the valve.
Fig. 3 in Sexually dimorphic ornamentation in modern spinicaudatans and the taxonomic implications for fossil clam shrimps
Fig. 3. Ornamentations on the growth bands of carapace of the extant spinicaudatan branchiopod Eocyzicus orientalis Daday, 1913, from Xinjiang, China. A. NIGP Cr. 1, male, ornamentation in the upper to middle parts of the carapace (A1), reticulate ornaments in the ventral part of the carapace (A2), dense pilosity on the growth lines near the edge of the carapace (A3). B. NIGP Cr. 2, female, ornamentation in the upper to middle parts of the carapace (B1), rows of nodular ornaments in the ventral part of the carapace (B2), stout setae on the growth lines near the edge of the carapace (B3).
Fig. 2 in Sexually dimorphic ornamentation in modern spinicaudatans and the taxonomic implications for fossil clam shrimps
Fig. 2. Ornamentation on the growth bands of carapaces of the extant spinicaudatan branchiopod Cyzicus sp., from Jilin, China. A. NIGP Cr. 141, male, ornamentation in the larval valve (A1), in the middle part of the carapace (A2), large reticulation and the radial lirae along the lower margin of the growth band (A3). B. NIGP Cr. 142, female, ornamentation in the larval valve (B1) and in the middle part of the carapace (B2), weakly ornamented area near the ventral margin (B3).
Fig. 8 in Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change
Fig. 8. Size comparison of squamosal versus face in Einiosaurus procurvicornis Sampson, 1995, subadult MOR 456 8-8-87-1 (A) and MOR 456 8-9-6-1, holotype (B, mirrored); squamosal superimposed in B. C. Outline of MOR 456 8-8-87-1 (red) superimposed over outline of MOR 456 8-9-6-1 (grey). D. Outline of MOR 591 (blue) superimposed over outline of MOR 456 8-9-6-1 (grey). Outlines aligned by otic notch.
Fig. 5 in Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change
Fig. 5. Lateral views of jugals of Einiosaurus procurvicornis Sampson, 1995, MOR 456 8-8-87-1 (A) and eucentrosauran (Einiosaurus procurvicornis or Achelousaurus horneri Sampson, 1995), MOR 591 (B, mirrored), from the Campanian Two Medicine Formation, Montana, USA. Arrow indicates epijugal.
Fig. 6 in Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change
Fig. 6. Ontogenetic series of supraorbital ornamentation of Einiosaurus procurvicornis Sampson, 1995 from the Campanian Canyon Bonebed, Two Medicine Formation (TM-046), Montana, USA. A, B. Juvenile, MOR 456 8-10-87-20 (A) and MOR 456 8-8-87-19 (B). C, D. Early subadult, MOR 456 8-9-7-3 (C) and MOR 456 2020-C-1 (D). E, F. Late subadult, MOR 456 8-8-87-1 (E) and MOR 456 8-23-87 (F). G, H. Young adult, MOR 456 2020-C-2 (G) and MOR 456 8-9-6-1 (H). B and D are mirrored. All specimens in anterior view, lateral is to the right in A–D, G, H; E, entire skull width; F, lateral is to the left.
Fig. 4 in Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change
Fig. 4. Anterior views of supraorbital ornamentation of Einiosaurus procurvicornis Sampson, 1995, MOR 456 8-8-87-1 (A) and eucentrosauran Einiosaurus procurvicornis or Achelousaurus horneri Sampson, 1995), MOR 591 (B), from the Campanian Two Medicine Formation, Montana, USA.
Fig. 7 in Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change
Fig. 7. Ontogenetic series of supraorbital ornamentation of Einiosaurus procurvicornis Sampson, 1995 from the Campanian Canyon Bonebed (TM-046), Montana, USA. A, B. Juvenile, MOR 456 8-10-87-20 (A) and MOR 456 8-8-87-19 (B). C, D. Early subadult, MOR 456 8-9-7-3 (C) and MOR 456 2020- C-1 (D). E, F. Late subadult, MOR 456 8-8-87-1 (E) and MOR 456 8-23-87 (F). G, H. Young adult, MOR 456 2020-C-2 (G) and MOR 456 8-9-6-1 (H). B, D–G are mirrored. All specimens in lateral view, anterior is to the left in all images.
Fig. 3 in Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change
Fig. 3. Right lateral views of supraorbital ornamentation of Einiosaurus procurvicornis Sampson, 1995, MOR 456 8-8-87-1 (A) and eucentrosauran (Einiosaurus procurvicornis or Achelousaurus horneri Sampson, 1995), MOR 591 (B) from the Campanian Two Medicine Formation, Montana, USA.
Fig. 2 in Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change
Fig. 2. Right lateral views of nasal horncores of Einiosaurus procurvicornis Sampson, 1995, MOR 456 8-8-87-1 (A) and eucentrosauran (Einiosaurus procurvicornis or Achelousaurus horneri Sampson, 1995), MOR 591 (B, mirrored), from the Campanian Two Medicine Formation, Montana, USA.
Fig. 1 in Comparative cranial osteology of subadult eucentrosauran ceratopsid dinosaurs from the Two Medicine Formation, Montana, indicates sequence of ornamentation development and complex supraorbital ontogenetic change
Fig. 1. Lateral views of articulated crania of subadult eucentrosaurans from the Campanian Two Medicine Formation, Montana, USA. A. Einiosaurus procurvicornis Sampson, 1995, MOR 456 8-8-87-1. B. Eucentrosauran (Einiosaurus procurvicornis or Achelousaurus horneri Sampson, 1995), MOR 591. Photographs (A1 and B1), osteological line drawings (A2, B2). Face of MOR 591 mirrored, with parietosquamosal frill superimposed. The contact outlines between the postorbital, jugal, and squamosal in A2 are estimated due to lack of externally visible sutures and may appear different from MOR 591 due to some breaks and gaps. P4–P7, parietal processes.
Fig. 1 in Invasion risks posed by ornamental freshwater fish trade to southeastern Brazilian rivers
Fig. 1. Cities and watersheds within the Minas Gerais State, Brazil, where the 39 ornamental fish stores were visited.
Fig. 2. A in Invasion risks posed by ornamental freshwater fish trade to southeastern Brazilian rivers
Fig. 2. A model describing the invasion stages that species must pass in order to represent an invasion risk for rivers in Minas Gerais State, Brazil.
Figure 1 in Trophic relationships among three species of ornamental fish from the region of Lake Amanã, Amazon
Figure 1. (A) Feed Strategy Carnegiella marthae. (1) Ephemenoptera (N), Diptera (L + A), Chironomidae (L) and Coleoptera (A); (2) Scales of fish; (3) Fragments of plants and insects. Points over an item indicates that they are overlapped; (B) Feed Strategy Carnegiella strigata. (1) Hymenoptera (A); (2) Coleoptera (A); (3) insect fragments; (4) fragments of plants; (5) Ephemenoptera (N); (6) Lepidoptera (L); (7) Chironomidae (L) and Gerridae (A + L). The points-arrested over an item indicates that they are overlapping; (C) Feed Strategy Gnathocharax steindachneri. (1) Chaoboridae (A); (2) Gerridae (N + A); (3) Hymenoptera (A); (4) fragments of insects; (5) fish scales; (6) Diptera (larvae + adults); (7) Coleoptera (A) and vegetable fragments; (8) Collembola, Homoptera (L) and Lepidoptera (L). Points over an item indicates that they are overlapped.
Fig. 6 in Adult identity crisis in Leucothrips (Thysanoptera: Thripidae) associated with the tropical ornamental plant Codiaeum variegatum (Euphorbiaceae)
Fig. 6. Divergence in the internal transcribed spacer 2 (ITS2) DNA sequence of Leucothrips specimens from Sechium edule in Costa Rica relative to those from other hosts. Sequences were aligned with MAFFT v7.293 using the G-INS-1 strategy.
Figs. 1–4 in Adult identity crisis in Leucothrips (Thysanoptera: Thripidae) associated with the tropical ornamental plant Codiaeum variegatum (Euphorbiaceae)
Figs. 1–4. Second instar larva of Leucothrips species: (1) morphotype-A abdominal tergite II spiracle at 1000× magnification; (2) morphotype-A prothorax; arrow indicates setae D6; (3) morphotype-B abdominal tergite II spiracle at 1000× magnification; (4) morphotype-B prothorax; arrow indicates setae D6; scale = 50 µm.
Fig. 5 in Adult identity crisis in Leucothrips (Thysanoptera: Thripidae) associated with the tropical ornamental plant Codiaeum variegatum (Euphorbiaceae)
Fig. 5. An unweighted pair group method with arithmetic mean (UPGMA) tree of Kimura 2-parameter distances (K2P) among the cytochrome oxidase c subunit 1 gene (COI) sequences of Leucothrips collections that are indistinguishable based on adult morphology. The optimal tree with the sum of branch length = 0.19814793 is shown. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches. The tree is drawn to scale. Analyses were conducted in MEGA version 6.
Fig 1 in Host specificity evaluation for Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae) on ornamental Ficus (Rosales: Moraceae)
Fig 1. Cage setup for Ficus benjamina variety choice test with Gynaikothrips uzeli in the greenhouse (year 2).
Fig. 4 in Direction and timing of dispersal of Scirtothrips dorsalis (Thysanoptera: Thripidae) on select ornamental host plant species in south Florida
Fig. 4. Flight behavior of Scirtothrips dorsalis during the day. Mean hourly captures of adults at (A) greenhouse and (B) field sites of TREC and MREC by the time sampled and cumulative degree-hours. Symbols represent means ± SD. An asterisk (*) indicates a significant difference between test locations at a given time based on a t-test at P ≤ 0.05.
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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.