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313 results for “Family history”
Research data for "Hutters in the Zamoyski Family Entail - history of an environmentally conditioned social group"
<p>Research data for "Hutters in the Zamoyski Family Entail - history of an environmentally conditioned social group" (v1_2024)</p>
Linked collectors and determiners for: Family groups of Diopsoidea and Nerioidea (Diptera: Schizophora) - Definition, history and relationships.
Natural history specimen data linked to collectors and determiners held within, "Family groups of Diopsoidea and Nerioidea (Diptera: Schizophora) - Definition, history and relationships". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/ffaf3b73-8bfe-499d-9073-0ce8c104e078">https://bionomia.net/dataset/ffaf3b73-8bfe-499d-9073-0ce8c104e078</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/ffaf3b73-8bfe-499d-9073-0ce8c104e078">https://gbif.org/dataset/ffaf3b73-8bfe-499d-9073-0ce8c104e078</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: UPNG Natural History Collection Plant Family Acanthaceae to Anacardiaceae.
Natural history specimen data linked to collectors and determiners held within, "UPNG Natural History Collection Plant Family Acanthaceae to Anacardiaceae". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/70eea0dd-92cb-4e40-b8cc-3c3913641277">https://bionomia.net/dataset/70eea0dd-92cb-4e40-b8cc-3c3913641277</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/70eea0dd-92cb-4e40-b8cc-3c3913641277">https://gbif.org/dataset/70eea0dd-92cb-4e40-b8cc-3c3913641277</a>. Formatted as a Frictionless Data package.
Figure 6 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)
Figure 6. Time calibration using the program BEAST. The error bar on each node represents the 95% confidence interval calculated by the program. The column on the right shows the time slice of Isthmian closure (3.5–2.5 Mya; Coates & Obando, 1996). Pli + Ple: Pliocene + Pleistocene.
Figure 4 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)
Figure 4. Strict consensus of three most parsimonious trees produced from 3373 aligned characters (TL = 3337; CI = 0.43; RI = 0.59) using maximum parsimony. Of these, 2315 are constant characters and 798 are potentially parsimony-informative. Numbers above and below branches are bootstrap (> 50%) and Bremer values, respectively.
Figure 3. A, the single most parsimonious tree derived from 2129 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)
Figure 3. A, the single most parsimonious tree derived from 2129 aligned characters of mitochondrial genes (12S, 16S, cyt-b) (CI = 0.40; TL = 31; RI = 0.58) using maximum parsimony. Of these, 1229 characters are constant and 708 characters are parsimony-informative. Numbers above branches are bootstrap values and below are Bremer values. B, strict consensus of 96 trees generated from 1244 aligned characters of nuclear genes (Rag1 and Cmos) (CI = 0.82; TL = 205; RI = 0.84) using maximum parsimony. Of these, 1086 characters are constant and 90 are parsimonyinformative. Numbers above branches are bootstrap values and below are Bremer values.
Figure 2 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)
Figure 2. Previous hypotheses regarding the position of Rhinoclemmys among geoemydids (upper cladograms) and the relationships among the species of the genus (lower cladograms). †Fossil taxon.
Unraveling the evolutionary history of the snakefly family Inocelliidae (Insecta: Raphidioptera) through integrative phylogenetics
<p>Inocelliidae is one of the two extant families of the holometabolan order Raphidioptera (snakeflies), with the modern fauna represented by seven genera and 44 species. The evolutionary history of the family is little known. Here we present the first phylogenetic and biogeographic analyses based on a worldwide sampling of taxa and datasets combined with morphological characters and mitochondrial genomes, aiming to investigate the intergeneric phylogeny and historical biogeography of Inocelliidae. The phylogenetic inference from the combined analysis of morphological and molecular data recovered the sister-group relationship between a clade of (<em>Negha</em> + <em>Indianoinocellia</em>) + <em>Sininocellia</em> and a clade of <em>Fibla</em> + the <em>Inocellia</em> clade (interiorly nested by <em>Amurinocellia</em> and <em>Parainocellia</em>). <em>Amurinocellia</em> <strong>stat. rev.</strong> and <em>Parainocellia</em><strong> stat. rev. et emend. nov.</strong> are relegated to subgeneric status within Inocellia, while a newly erected subgenus of <em>Inocellia</em>, <em>Epinocellia</em> <strong>subgen. nov.</strong>, accommodates the former <em>Parainocellia</em> <em>burmana</em> (U. Aspöck and H. Aspöck, 1968) plus a new species <em>Inocellia</em> (<em>Epinocellia</em>) weii sp. nov. Further, the <em>Inocellia</em> crassicornis group constitutes the nominate subgenus <em>Inocellia</em> <strong>stat. nov</strong>., but the <em>Inocellia</em> <em>fulvostigmata</em> group is paraphyletic. Diversification within Inocelliidae is distinguished by an Eocene divergence leading to extant genera and a Miocene radiation of species. A biogeographic scenario depicts how the diverse inocelliid fauna from East Asia could have originated from western North America via dispersal across the Beringia during the early Tertiary, and how the Miocene ancestors of <em>Inocellia</em> could have accomplished long-distance dispersals via the Tibet‐Himalayan corridor or eastern Palaearctic to western Palaearctic. Our results shed new light specifically on the evolution of Inocelliidae and, in general, the Raphidioptera.</p>
Figure 1 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)
Figure 1. Distribution of the family Geoemydidae (data compiled from Iverson, 1992).
Data from: Little bits of dragonfly history repeating exemplified by a new Pennsylvanian family
<p>During its 320 million years evolution, dragon- and damselflies (Odonata) wing morphology underwent intense modifications. The resulting diversity prompted comparative analyses focusing on phylogeny. However, homoplasy proved to plague wing-related characters. Concurrently, limited benefits were obtained from considering fossil taxa, similarly impacted. Herein we investigate two aspects particularly affected by convergence, namely the acquisition of vein-like structuring elements derived from regular cross-venation, termed conamina; and the evolution of butter knife wing shape. Conamen implementation is found to be consistently linked with vein curvature sharpening, itself generating potential breaking points. Conamina therefore likely evolved to address wing integrity issues during ever-more-demanding flight performance. Moreover, an existing conamen is likely to trigger the acquisition of further, associated conamina. As for butter knife shape, previously documented in the extinct Archizygoptera and among damselflies, we report a new, 315-million-years-old occurrence with the rare species <em>Haidilaozhen</em> <em>cuiae</em> gen. et sp. nov. (family Haidilaozhenidae fam. nov.), from the Xiaheyan locality (China). The repeated acquisition of butter-knife-shaped wing can be related to slow-speed flight and, in turn, predator avoidance. In both cases of iterated regularities, the unique 'network-and-membrane' wing design proper to insects is found to compose a strong, constraining factor.</p>
Intravenous Alcohol Administration Using BrAc Method in Healthy Subjects With and Without a Family History of Alcoholism
ClinicalTrials.gov study NCT00612352. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Ketamine/Placebo Family History Positive Study
ClinicalTrials.gov study NCT00588952. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Characterizing the Effects of Family History of Alcoholism on Alcohol Analgesia
ClinicalTrials.gov study NCT04925076. IPD Sharing: NO. Countries: 1. Publications: 2.
Impact of Family History and Decision Support on High-risk Cancer Screening
ClinicalTrials.gov study NCT02247336. IPD Sharing: NO. Countries: 1. Publications: 2.
Family Health History in Diverse Care Settings (FHH)
ClinicalTrials.gov study NCT01956773. IPD Sharing: Not stated. Countries: 1. Publications: 4.
Family History and Cancer Risk Study
ClinicalTrials.gov study NCT05079334. IPD Sharing: NO. Countries: 1. Publications: 1.
Educational CD-ROM Compared With Standard Informed Consent for Patients With Colorectal Cancer or a Family History of Colorectal Cancer
ClinicalTrials.gov study NCT00450424. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Data from: Little bits of dragonfly history repeating exemplified by a new Pennsylvanian family
Open the record for dataset details and reuse information.
Data from: Assessing completeness of cancer family history in EHRs using genetically-defined kinships: a cross-sectional study
Open the record for dataset details and reuse information.
A family history: Effects of parental age on offspring life-history traits in bighorn sheep
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.