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268 results for “Emperors,”
Total number of Roman imperial portraits, per emperor (N=2135), excluding imperial portraits of unknown emperors
<p>The figure presented here includes the total number of sculptural portraits of Roman emperors (mostly carved from marble or casted in bronze) that were collected for the purposes of analyzing the representation of Roman emperors in freestanding sculpture. PhD dissertation: S. Heijnen (2022), Portraying Change: The Representation of Roman Emperors in Freestanding Sculpture (ca. 50 BC - ca. 400 AD). Dissertation. Radboud University.</p>
Number of imperial portraits (average), per year of reign (N=1625), excluding emperors that ruled less than a year and imperial portraits that circulated prior to the emperor's accession
<p>The figure presented here includes the average number of sculptural portraits of Roman emperors (mostly carved from marble or casted in bronze), per year of rule, that were collected for the purposes of analyzing the representation of Roman emperors in freestanding sculpture. PhD dissertation: S. Heijnen (2022), Portraying Change: The Representation of Roman Emperors in Freestanding Sculpture (ca. 50 BC - ca. 400 AD). Dissertation. Radboud University.</p>
Fig. 4 in First Specimen-based Records of Redfin Emperor Monotaxis heterodon (Perciformes: Lethrinidae) from Japan, with New Diagnostic Characters Applicable to Identification of Preserved Specimens
Fig. 4. Eyes (A, B), occipital region (C, D), and inner surface of pectoral-fin base (E, F) of M. heterodon (A, C, E) and M. grandoculis (B, D, F), showing differences between the two species. A, KAUM–I. 88394, 215.0 mm SL, fresh condition; B, D, F, KAUM–I. 46014, 185.5 mm SL, fresh (B) and preserved (D, F) conditions; C, E, URM-P 34768, 189.1 mm SL, preserved condition.
Fig. 3 in First Specimen-based Records of Redfin Emperor Monotaxis heterodon (Perciformes: Lethrinidae) from Japan, with New Diagnostic Characters Applicable to Identification of Preserved Specimens
Fig. 3. Relationships of (A) snout length (excluding lips) (% of SL) and (B) spinous anal-fin base length (% of SL) to SL (mm) in M. heterodon (red circles) and M. grandoculis (blue triangles).
Fig. 2 in First Specimen-based Records of Redfin Emperor Monotaxis heterodon (Perciformes: Lethrinidae) from Japan, with New Diagnostic Characters Applicable to Identification of Preserved Specimens
Fig. 2. Fresh (A) and preserved (B) specimen of Monotaxis grandoculis (KAUM–I. 46014, 185.5 mm SL) from Yoron-jima island, Amami Islands, Japan.
Fig. 1 in First Specimen-based Records of Redfin Emperor Monotaxis heterodon (Perciformes: Lethrinidae) from Japan, with New Diagnostic Characters Applicable to Identification of Preserved Specimens
Fig. 1. Fresh (A) and preserved (B) specimen of Monotaxis heterodon (KAUM–I. 88394, 215.0 mm SL) from Ryukyu Islands, Japan.
Fig. 1 in Identification of the Commercially Important Oreosomatid Fish (Zeiformes: Teleostei) of the Emperor Seamounts, with Comments on Diagnostic Characters of the Species
Fig. 1. Lateral view of oreosomatids. A, Allocyttus folletti from the Emperor Seamounts, SNFR 22402, 289.8 mm SL; B, Allocyttus verrucosus from New Zealand, NSMT-P 41168, 187.2 mm SL; caudal peduncle of A. folletti; C, SNFR 10560, 293.4 mm SL, Emperor Seamounts, and that of A. verrucosus; D, NSMT-P 41168, 187.2 mm SL, New Zealand; nasal of oreosomatids; E, A. folletti, SNFR 10561, 347 mm SL, Emperor Seamounts; F, A. verrucosus, NSMT-P 113107, 238.4 mm SL, west coast of Australia. Abbreviations: NA, nasal; PN, posterior nostril.
Fig. 3 in Identification of the Commercially Important Oreosomatid Fish (Zeiformes: Teleostei) of the Emperor Seamounts, with Comments on Diagnostic Characters of the Species
Fig. 3. Lateral aspect (above) and abdomen (below) of Allocyttus folletti. A, SNFR 10560, 293.4 mm SL, Emperor Seamounts; B, CAS-SU 15377, holotype of Allocyttus folletti, off California, traced from Myers (1960: fig. 1). Arrows indicate the rows of scutes.
Fig. 2 in Identification of the Commercially Important Oreosomatid Fish (Zeiformes: Teleostei) of the Emperor Seamounts, with Comments on Diagnostic Characters of the Species
Fig. 2. Scales on mid-side of body in, (A) Allocyttus folletti, FAKU 72575, 397 mm SL, Emperor Seamounts, and (B) Allocyttus verrucosus, NSMT-P 113107, 238.4 mm SL, Australia; enlarged scales of dorsal-fin base (S-DFB) in (C) A. folletti, SNFR 22403, 289.3 mm SL, Emperor Seamounts, and (D) A. verrucosus, BSKU 48476, 136.5 mm SL, off South Africa.
Рис. 7–9. Coelorinchus idiolepis sp. nov. (7 — гоΛотип, 8 — паратип) и C. anisacanthus, гоΛотип, 81,5 мм HL (9), гоΛова, виΔ сбоку. Обозначения: oo — Δиаметр гΛаза, po — посторбитаΛьная ΔΛина. Масштаб: 7 — 20 мм; 8, 9 — 10 мм Figs. 7–9. Coelorinchus idiolepis sp. nov. (7 — holotype, 8 — paratype) and C. anisacanthus, holotype, 81.5 mm HL (9), head, lateral view. Symbols: oo — diameter of eye, po — postorbital length. Scale bars: 7 — 20 mm; 8, 9 — 10 mm in Coelorinchus From The Hawaiian-Emperor Seamount Chain (The Pacific Ocean) (Teleostei, Gadiformes, Macrouridae)
Рис. 7–9. Coelorinchus idiolepis sp. nov. (7 — гоΛотип, 8 — паратип) и C. anisacanthus, гоΛотип, 81,5 мм HL (9), гоΛова, виΔ сбоку. Обозначения: oo — Δиаметр гΛаза, po — посторбитаΛьная ΔΛина. Масштаб: 7 — 20 мм; 8, 9 — 10 мм Figs. 7–9. Coelorinchus idiolepis sp. nov. (7 — holotype, 8 — paratype) and C. anisacanthus, holotype, 81.5 mm HL (9), head, lateral view. Symbols: oo — diameter of eye, po — postorbital length. Scale bars: 7 — 20 mm; 8, 9 — 10 mm
Рис. 10–20. Coelorinchus idiolepis sp. nov., изоΛированные чешуи (10–17 — гоΛотип, 18–20 — паратип): 10, 11 — преΔорсаΛьная обΛасть; 12, 13, 18 — истмус; 14–16 — бока теΛа в интерΔорсаΛьном промежутке; 17 — абΔомен; 19, 20 — бока теΛа наΔ основанием груΔного пΛавника. Масштаб: 10–17 — 2,5 мм (Λинейка общая); 18–20 — 1,5 мм (Λинейка общая) in Coelorinchus From The Hawaiian-Emperor Seamount Chain (The Pacific Ocean) (Teleostei, Gadiformes, Macrouridae)
Рис. 10–20. Coelorinchus idiolepis sp. nov., изоΛированные чешуи (10–17 — гоΛотип, 18–20 — паратип): 10, 11 — преΔорсаΛьная обΛасть; 12, 13, 18 — истмус; 14–16 — бока теΛа в интерΔорсаΛьном промежутке; 17 — абΔомен; 19, 20 — бока теΛа наΔ основанием груΔного пΛавника. Масштаб: 10–17 — 2,5 мм (Λинейка общая); 18–20 — 1,5 мм (Λинейка общая)
FIGURE 1 in A New Grenadier Fish of the Genus Lucigadus (Macrouridae, Gadiformes, Teleostei) from the Emperor Seamounts, Northwestern Pacific
FIGURE 1. Emperor Seamounts chain in the northwestern Pacific, extending north-south along approximately the 170° meridian from about latitude 55°N southward to 30°N. (http://nwpbfo.nomaki.jp/fisheries.html)
Fig. 6 in Negligible evidence for detrimental effects of Leucocytozoon infections among Emperor Geese (Anser canagicus) breeding on the Yukon-Kuskokwim Delta, Alaska
Fig. 6. Comparison of mass measures for incubating adult female Emperor Geese infected with Leucocytozoon parasites genetically characterized in this study L. simondi clade A (blue), L. simondi clade B (red), or other/mixed Leucocytozoon (grey; see Materials and methods) using boxplots (Panel A) and plotted by incubation day (Panel B). The trendline in panel B is depicts predicted mass given the day of incubation and positive Leucocytozoon infection status from our top-ranking regression model (see Results). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 5. Phylogenetic tree depicting inferred genetic relationships among Leucocytozoon mitochondrial DNA cytochrome b in Negligible evidence for detrimental effects of Leucocytozoon infections among Emperor Geese (Anser canagicus) breeding on the Yukon-Kuskokwim Delta, Alaska
Fig. 5. Phylogenetic tree depicting inferred genetic relationships among Leucocytozoon mitochondrial DNA cytochrome b haplotypes identified from blood samples collected from Emperor Geese inhabiting the Yukon-Kuskokwim Delta, Alaska during 2006–2016 and those previously reported for closely related haemosporidian morphospecies on the National Center for Biotechnology Information GenBank and Malavi databases (accession IDs in parentheses). Bars to the right of tree represent the assignment of sequences to L. simondi clade A (teal), L. simondi clade B (orange), or other Leucocytozoon. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4. Phylogenetic tree depicting inferred genetic relationships among Haemoproteus mitochondrial DNA cytochrome b in Negligible evidence for detrimental effects of Leucocytozoon infections among Emperor Geese (Anser canagicus) breeding on the Yukon-Kuskokwim Delta, Alaska
Fig. 4. Phylogenetic tree depicting inferred genetic relationships among Haemoproteus mitochondrial DNA cytochrome b haplotypes identified from blood samples collected from Emperor Geese inhabiting the Yukon-Kuskokwim Delta, Alaska during 2006–2016 and those previously reported for closely related haemosporidian morphospecies on the National Center for Biotechnology Information GenBank and Malavi databases (accession IDs in parentheses).
Fig. 1 in Negligible evidence for detrimental effects of Leucocytozoon infections among Emperor Geese (Anser canagicus) breeding on the Yukon-Kuskokwim Delta, Alaska
Fig. 1. Mass of adult female nesting Emperor Geese per day of incubation for birds infected (red) and uninfected (black/white) with Leucocytozoon parasites using samples collected on the Yukon-Kuskokwim Delta, Alaska during 2006–2016. Trend lines indicate the predicted mass for an individual goose throughout the incubation period from day 11 based upon on the top supported model (Mass ~ Inc + Leu). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2. Minimum spanning network for haemosporidian mitochondrial DNA cytochrome b haplotypes identified from blood samples collected from Emperor Geese inhabiting the YukonKuskokwim Delta, Alaska during 2006–2016 in Negligible evidence for detrimental effects of Leucocytozoon infections among Emperor Geese (Anser canagicus) breeding on the Yukon-Kuskokwim Delta, Alaska
Fig. 2. Minimum spanning network for haemosporidian mitochondrial DNA cytochrome b haplotypes identified from blood samples collected from Emperor Geese inhabiting the YukonKuskokwim Delta, Alaska during 2006–2016. Circles are drawn proportional to the frequency at which haplotypes were detected. Shading represented the assignment of representative sequences for haplotypes to L. simondi clade A (teal), L. simondi clade B (orange), or other Leucocytozoon (grey) in phylogenetic analyses (see Results and Fig. 5). Lines are drawn proportional to genetic distance and are labeled per the number of mutations represented (except single nucleotide polymorphisms which are unlabeled). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Linked collectors and determiners for: Lethrinus ravus, a new species of emperor fish (Perciformes: Lethrinidae) from the western Pacific and eastern Indian oceans..
Natural history specimen data linked to collectors and determiners held within, "Lethrinus ravus, a new species of emperor fish (Perciformes: Lethrinidae) from the western Pacific and eastern Indian oceans.". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/d1ac76ee-4d54-4cbf-aa32-a0559c72b730">https://bionomia.net/dataset/d1ac76ee-4d54-4cbf-aa32-a0559c72b730</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/d1ac76ee-4d54-4cbf-aa32-a0559c72b730">https://gbif.org/dataset/d1ac76ee-4d54-4cbf-aa32-a0559c72b730</a>. Formatted as a Frictionless Data package.
Global analysis of emperor penguin populations
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Emperor Nero
Youthful portrait of the emperor Nero (AD 37-68). Roman, around 60 AD. Archaeological Museum, Corinth, Italy. Photogrammetric Model: Agisoft Photoscan, Autodesk Memento, Meshmixer. Source: Objaverse 1.0 / Sketchfab
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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.