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3,101 results for “Historical”
Fig. 15 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 15. Apodrosus quisqueyanus. (A) habitus, dorsal view; (B) head, frontal view; (C) habitus, lateral view; (D) habitus, ventral view; (E) and (F) aedeagus in dorsal and lateral view, respectively; (G) spermatheca. This figure is published in colour in the online version of this journal, which can be accessed via http:// www.brill/ise
Fig. 13 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 13. Apodrosus viridium. (A) habitus, dorsal view; (B) head, frontal view; (C) habitus, lateral view; (D) habitus, ventral view; (E) and (F) aedeagus in dorsal and lateral view, respectively; (G) spermatheca. This figure is published in colour in the online version of this journal, which can be accessed via http:// www.brill/ise
Fig. 21 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 21. DIVA reconstruction of ancestral areas for the species of Apodrosus and the most closely related Anypotactus (under the command "maxareas=2"; 17 splitting events). The optimized areas are displayed at the right end of each branch; joint ancestral areas are linked with a comma and alternative optimizations are separated with a forward slash.
Fig. 18 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 18. Occurrences of Apodrosus species in (A) the Bahamas (Grand Bahama and Andros Island) and (B) Hispaniola, Mona Island, and the Turks and Caicos Islands.
Fig. 7 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 7. Apodrosus andersoni. (A) habitus, dorsal view; (B) head, frontal view; (C) habitus, lateral view; (D) habitus, ventral view; (E) and (F) aedeagus in dorsal and lateral view, respectively; (G) spermatheca. This figure is published in colour in the online version of this journal, which can be accessed via http:// www.brill/ise
Fig. 10 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 10. Apodrosus eximius. (A) habitus, dorsal view; (B) head, frontal view; (C) habitus, lateral view; (D) habitus, ventral view; (E) and (F) aedeagus in dorsal and lateral view, respectively; (G) spermatheca. This figure is published in colour in the online version of this journal, which can be accessed via http:// www.brill/ise
Fig. 6 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 6. Apodrosus artus. (A) habitus, dorsal view; (B) head, frontal view; (C) habitus, lateral view; (D) habitus, ventral view; (E) and (F) aedeagus in dorsal and lateral view, respectively. This figure is published in colour in the online version of this journal, which can be accessed via http://www.brill/ise
Fig. 8 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 8. Apodrosus earinusparsus. (A) habitus, dorsal view; (B) head, frontal view; (C) habitus, lateral view; (D) habitus, ventral view; (E) and (F) aedeagus in dorsal and lateral view, respectively; (G) spermatheca. This figure is published in colour in the online version of this journal, which can be accessed via http:// www.brill/ise
Fig. 5 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 5. Apodrosus wolcotti, female terminalia. (A) sternum VIII; (B) and (C) coxites in dorsal and lateral view, respectively; (D) spermatheca.
Fig. 2 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 2. (A) Apodrosus epipolevatus, head, ventral view; (B) A. argentatus, mandibles with deciduous processes attached; (C) A. wolcotti, right maxilla, ventral view; (D) A. wolcotti, labial prementum, ventral view. This figure is published in colour in the online version of this journal, which can be accessed via http:// www.brill/ise
Fig. 23. Preferred area cladogram for Apodrosus, selected among six alternative cladograms produced under assumption 2 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 23. Preferred area cladogram for Apodrosus, selected among six alternative cladograms produced under assumption 2 with component analysis, with inferred ancestral areas mapped on the main internal branch. Area labels as in Fig. 21. See text for further detail.
Fig. 12 in Revision, phylogeny and historical biogeography of the genus Apodrosus Marshall, 1922 (Coleoptera: Curculionidae: Entiminae)
Fig. 12. Apodrosus mammuthus. (A) habitus, dorsal view; (B) head, frontal view; (C) habitus, lateral view; (D) habitus, ventral view; (E) and (F) aedeagus in dorsal and lateral view, respectively; (G) spermatheca. This figure is published in colour in the online version of this journal, which can be accessed via http:// www.brill/ise
Historical translocations and stocking alter the genetic structure of a Mediterranean lobster fishery
Stocking is often used to supplement wild populations that are overexploited or have collapsed, yet it is unclear how this affects the genetic diversity of marine invertebrate populations. During the 1970s, a lobster stock enhancement programme was carried out around the island of Corsica in the Mediterranean using individuals translocated from the Atlantic coast of France. This included the release of thousands of hatchery-reared post-larval lobsters and several adult individuals, but no monitoring plan was established to assess whether these animals survived and recruited to the population. In this study, we sampled European lobster (<i>Homarus gammarus</i>) individuals caught around Corsica and tested whether they showed Atlantic ancestry. Due to a natural marked phylogeographic break between Atlantic and Mediterranean lobsters, we hypothesised that lobsters with dominant (>0.50) Atlantic ancestry were descended from historical stocking releases. Twenty Corsican lobsters were genotyped at 79 single nucleotide polymorphisms and assignment analysis showed that the majority (13) had dominant Atlantic ancestry. This suggests that the hatchery stocking programme carried out in Corsica during the 1970s, using individuals translocated from the Atlantic coast of France, has likely augmented local recruitment but at a cost of altering the genetic structure of the Corsican lobster population.
RIBuild: Material properties for historic building materials and insulation materials
<p>This dataset consists of</p> <p>1) Excel sheets with material properties for a) a collection of historic building materials and b) insulation materials suited for internal insulation. Material properties were collected from all RIBuild partner countries. The main purpose was to locate data set not included in the DELPHIN database that contained the needed data for DELPHIN simulations.</p> <p>2) Excel sheets with material properties for specific historic building materials used in Italy and Switzerland. As these materials were supposed to be included in hygrothermal simulations with DELPHIN performed in RIBuild, a full material characterization was required as described in RIBuild deliverable D2.1 and in the DELPHIN specifications. Material characterization was performed at RTU.</p> <p>Requirements concerning input need for DELPHIN simulations are described in RIBuild deliverable D2.1.</p> <p>Overview of data files to be found in 'RIBuild data WP2 Mat Prop' as part of this dataset.</p> <p> </p>
RIBuild: Survey of historic building stock - with case studies on renovation
<p>Database prepared in Excel including four elements, as background information for RIBuild Deliverable D1.1 about the historic building stock:</p> <p>Historic buildings stock energy consumption (1)</p> <p>Historic building stock description (2)</p> <p>Building construction elements (3)</p> <p>Case studies (4)</p> <p>Element (1)-(3) are referring to the historic building stock in RIBuild partner countries in general, while element (4) contains examples of carried out renovation projects, involving internal insulation of a historic building.</p> <p>If available, the case study sheets contain information about the floor area, present use, the building envelope (thickness, materials), renovation history, pre- and post-energy usage and renovation cost. Further, information about typical defects and the main driving forces for the renovation project, planning or design tools used, whether the goal with the renovation was achieved and the satisfaction of the users.</p> <p>Overview of data files to be found in 'RIBuild data WP1' as part of this dataset.</p>
Historical Issue Data of Projects on Jira
<p>This dataset contains all the historical issues from sixty-six Apache Open Source projects collected in February 2018. It was used in the paper “Traceability Network Analysis: A Case Study of Links In Issue Tracking Systems” published in the Seventh International Workshop on Artificial Intelligence and Requirements Engineering (AIRE'20) to study issue traceability as a network structure.</p>
ICFHR 2020 Competition on Image Retrieval for Historical Handwritten Fragments (HisFrag20) Dataset
<p>This competition investigates the performance of large-scale retrieval of historical document fragments based on writer recognition. The analysis of historic fragments is a difficult challenge commonly solved by trained humanists.<br> We focus on the task of automatic image retrieval to simulate common scenarios of humanities research, such as fragment or writer retrieval. Therefore, we created a large dataset consisting of more than 120000 fragments.<br> The goal is then to find similar patches of the same page or manuscript. contains ~100 000 fragments using the Historical-IR19 as base dataset, they should all contain some text, however some fragments are quite small.</p> <p>Training-set: contains ~100 000 fragments using the Historical-IR19 as base dataset, they should all contain some text, however some fragments are quite small.</p> <p>Test-set: contains about 20 000 new fragments</p> <p>Naming-convention: WID_PID_FID.jpg , where WID=writer id, PID: page id, FID= fragment id</p> <p>For more information visit: <a href="https://lme.tf.fau.de/research/competitions/hisfragir20/">https://lme.tf.fau.de/research/competitions/hisfragir20/</a></p>
Data from: Out of sight, out of mind: Widespread nuclear and plastid-nuclear discordance in the flowering plant genus Polemonium (Polemoniaceae) suggests widespread historical gene flow despite limited nuclear signal
Phylogenomic data from a rapidly increasing number of studies provide new evidence for resolving relationships in recently radiated clades, but they also pose new challenges for inferring evolutionary histories. Most existing methods for reconstructing phylogenetic hypotheses rely solely on algorithms that only consider incomplete lineage sorting as a cause of intra- or inter-genomic discordance. Here, we utilize a variety of methods, including those to infer phylogenetic networks, to account for both incomplete lineage sorting and introgression as a case for nuclear and cytoplasmic-nuclear discordance using phylogenomic data from the recently radiated flowering plant genus Polemonium (Polemoniaceae), an ecologically diverse genus in Western North America with known and suspected gene flow between species. We find evidence for widespread discordance among nuclear loci that can be explained by both incomplete lineage sorting and reticulate evolution in the evolutionary history of Polemonium. Furthermore, the histories of organellar genomes show strong discordance with the inferred species tree from the nuclear genome. Discordance between the nuclear and plastid genome is not completely explained by incomplete lineage sorting, and only one case of discordance is explained by detected introgression events. Our results suggest that multiple processes have been involved in the evolutionary history of Polemonium and that results from the plastid genome do not accurately reflect species relationships. We discuss several potential causes for this cytoplasmic-nuclear discordance, which emerging evidence suggests is more widespread across the Tree of Life than previously thought.
FIGURES 7–12 in Aphonopelma braunshausenii Tesmoingt, 1996 is a nomen dubium, with review of some historic morphological characters ineffective at species delineation (Araneae: Theraphosidae)
FIGURES 7–12. Labia of the above Aphonopelma specimens all showing near identical morphology in shape and cuspule density, 7 Aphonopelma platnicki holotype male BMNH 1894.2.18.1, 8 Aphonopelma clarki holotype female BMNH 1959.1.2 [= A. hentzi Girard, 1853 per Hamilton et al. 2016)], 9 Aphonopelma anax non-type male OUMNH 2009-001, 10 Aphonopelma pallidum holotype male BMNH 1898.12.24.34–37, 11 Aphonopelma bicoloratum non-type male OUMNH 2011-045, 12 Aphonopelma marxi non-type male OUMNH 2007-064. Scale lines = 1mm.
FIGURES 1–6 in Aphonopelma braunshausenii Tesmoingt, 1996 is a nomen dubium, with review of some historic morphological characters ineffective at species delineation (Araneae: Theraphosidae)
FIGURES 1–6. Ocular tubercles of some Aphonopelma species showing variation in size and distance between eyes, 1 Aphonopelma platnicki holotype male BMNH 1894.2.18.1, 2 Aphonopelma clarki holotype female BMNH 1959.1.2 [= A. hentzi Girard, 1853 per Hamilton et al. 2016)], 3 Aphonopelma anax non-type male OUMNH 2009-001, 4 Aphonopelma pallidum holotype male BMNH 1898.12.24.34–37, 5 Aphonopelma bicoloratum non-type male OUMNH 2011-045, 6 Aphonopelma marxi nontype male OUMNH 2007-064. Scale lines = 1mm.
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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.