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13,587 results for “specification”
The first comprehensive revision of all the species attributed to Melomys led J. I. Menzies in 1996 to resurrect the genus Paramelomys and to redefine its morphologicallimits and species content. Menzies created P. gressitti as a new species belonging to a group displaying morphological similarities and including also P. lorentzii and P. moncktoni. Monotypic Distribution. E New Guinea. Descriptive notes. Head-body 135-162 mm, hindfoot 30-34 mm; no specific data are available for body weight. Gressitt's Mosaic-tailed Rat is a medium-sized Paramelomys with a soft, thick and woolly pelage, a long narrow foot, and a tail with three hairs per scale. It exhibits a medium-sepia dorsal pelage and a gray-buff ventral one. Tail is slightly shorter (99%) than head-body length. The skull has a narrow zygomatic plate. Habitat. Moist tropical mountain forest between 2300 m and 2400 m. Food and Feeding. No information. Breeding. No information. Activity patterns. Gressitt's Mosaic-tailed Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List owing to its small geographic range (less than 3500 km?*) and the destruction ofits habitat by mining and logging activities. The major threat to Gressitt's Mosaic-tailed Rat is ongoing habitat degradation caused by nearby human populations; habitat on Mount Kandy has been destroyed by gold-miners and wood-cutters. Bibliography. Menzies (1996). in Muridae
The first comprehensive revision of all the species attributed to Melomys led J. I. Menzies in 1996 to resurrect the genus Paramelomys and to redefine its morphologicallimits and species content. Menzies created P. gressitti as a new species belonging to a group displaying morphological similarities and including also P. lorentzii and P. moncktoni. Monotypic Distribution. E New Guinea. Descriptive notes. Head-body 135-162 mm, hindfoot 30-34 mm; no specific data are available for body weight. Gressitt's Mosaic-tailed Rat is a medium-sized Paramelomys with a soft, thick and woolly pelage, a long narrow foot, and a tail with three hairs per scale. It exhibits a medium-sepia dorsal pelage and a gray-buff ventral one. Tail is slightly shorter (99%) than head-body length. The skull has a narrow zygomatic plate. Habitat. Moist tropical mountain forest between 2300 m and 2400 m. Food and Feeding. No information. Breeding. No information. Activity patterns. Gressitt's Mosaic-tailed Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List owing to its small geographic range (less than 3500 km?*) and the destruction ofits habitat by mining and logging activities. The major threat to Gressitt's Mosaic-tailed Rat is ongoing habitat degradation caused by nearby human populations; habitat on Mount Kandy has been destroyed by gold-miners and wood-cutters. Bibliography. Menzies (1996).
FIGURE 7 in Grismadox elsneri sp. nov.-a new species of ant-resembling sac spider from the Bolivian orocline, with indirect evidence of species-specific mimicry (Araneae: Corinnidae: Castianeirinae)
FIGURE 7. Live habitus of Grismadox elsneri sp. nov. and its putative ant models: A, female paratype (CBF); B, male holotype (IBSI-Ara 1710); C, Camponotus cf. crassus Mayr, 1862; D, C. cf. blandus (F. Smith, 1858).
FIGURE 5 in Grismadox elsneri sp. nov.-a new species of ant-resembling sac spider from the Bolivian orocline, with indirect evidence of species-specific mimicry (Araneae: Corinnidae: Castianeirinae)
FIGURE 5. Grismadox elsneri sp. nov., female genitalia: A, epigyne paratype (IBSI-Ara 1711), ventral; B, idem, dorsal (vulva); C, detail of CO, ventral; D, detail of ST, dorsal; E, detail of FD, dorsal (CO = copulatory opening; ST I = primary spermatheca; ST II = secondary spermathecae; FD = fertilization duct).
FIGURE 6 in Grismadox elsneri sp. nov.-a new species of ant-resembling sac spider from the Bolivian orocline, with indirect evidence of species-specific mimicry (Araneae: Corinnidae: Castianeirinae)
FIGURE 6. Grismadox elsneri sp. nov.: A, habitat, savanna grassland at the edge of Chiquitano forest; B, female paratype (CBF), life habitus in habitat, on a dry grass leaf.
FIGURE 3 in Grismadox elsneri sp. nov.-a new species of ant-resembling sac spider from the Bolivian orocline, with indirect evidence of species-specific mimicry (Araneae: Corinnidae: Castianeirinae)
FIGURE 3. Grismadox elsneri sp. nov., palp, male holotype (IBSI-Ara 1710): A, ventral view; B, retrolateral view; C, bulb, ventral view; D, detail of embolus, ventral view (dRTA = dorso-retrolateral tibial apophysis; vRTA = ventro-retrolateral tibial apophysis).
FIGURE 4 in Grismadox elsneri sp. nov.-a new species of ant-resembling sac spider from the Bolivian orocline, with indirect evidence of species-specific mimicry (Araneae: Corinnidae: Castianeirinae)
FIGURE 4. Grismadox elsneri sp. nov., paratype female (IBSI-Ara 1711): A, dorsal; B, ventral; C, lateral. Please note that most setae are broken off due to storage in ethanol. Scale bars 0.5 mm.
FIGURE 2 in Grismadox elsneri sp. nov.-a new species of ant-resembling sac spider from the Bolivian orocline, with indirect evidence of species-specific mimicry (Araneae: Corinnidae: Castianeirinae)
FIGURE 2. Grismadox elsneri sp. nov., holotype male (IBSI-Ara 1710): A, dorsal; B, ventral; C, lateral. Please note that most setae are broken off due to storage in ethanol. Scale bars 0.5 mm.
FIGURE 1 in Grismadox elsneri sp. nov.-a new species of ant-resembling sac spider from the Bolivian orocline, with indirect evidence of species-specific mimicry (Araneae: Corinnidae: Castianeirinae)
FIGURE 1. Ecoregion distribution of Grismadox elsneri sp. nov., according to the regionalization by Navarro & Ferreira (2007); A, Bolivia; B, Sub-Andean area at the Bolivian orocline; 1, Santa Cruz de la Colina, Urubo, Santa Cruz department; map produced with QGIS (version 2.14.3, http:// www.qgis.org/en/site).
Otomys cheesmani previously was included in O.typus but shown to be a distinct spe-cies based on morphological and molecular grounds. Monotypic. Distribution. Restricted to two known lo-calities in NW Ethiopia, S ofLake Tana. Descriptive notes. Head-body 165-210 mm, tail 77-106 mm, ear 22-24 mm, hindfoot 28-31 mm. No specific data are available for body weight. Cheesman's Vlei Rat has shaggy dark pelage and is larger than all other species of Otomys, except the Angolan Vlei Rat (O. anchietae). Fur of Cheesman's Vlei Rat is bright brown, with reddish shade above and pale yellowish gray below. Ears are blackish, and inner surfaces are covered with short rufous hairs. Forefeet and hindfeet are dark gray above. Tail is relatively short (49-3% of head-body length), blackish above and pale yellowish below but notappearing distinctly bicolored. Lower incisors with two deep grooves. M, has four laminae, and M" has eight or nine laminae. in Muridae
Otomys cheesmani previously was included in O.typus but shown to be a distinct spe-cies based on morphological and molecular grounds. Monotypic. Distribution. Restricted to two known lo-calities in NW Ethiopia, S ofLake Tana. Descriptive notes. Head-body 165-210 mm, tail 77-106 mm, ear 22-24 mm, hindfoot 28-31 mm. No specific data are available for body weight. Cheesman's Vlei Rat has shaggy dark pelage and is larger than all other species of Otomys, except the Angolan Vlei Rat (O. anchietae). Fur of Cheesman's Vlei Rat is bright brown, with reddish shade above and pale yellowish gray below. Ears are blackish, and inner surfaces are covered with short rufous hairs. Forefeet and hindfeet are dark gray above. Tail is relatively short (49-3% of head-body length), blackish above and pale yellowish below but notappearing distinctly bicolored. Lower incisors with two deep grooves. M, has four laminae, and M" has eight or nine laminae.
Evidence from the Literature to Answer Specific Research Questions
<p>All the relevant information that was extracted from the 21 selected articles to answer the four specific research questions (SRQ1, SRQ2, SRQ3, and SRQ4) are presented in a form of a complete table.</p>
Relocations for: Satellite-tracking reveals sex-specific migration distance in green turtles (Chelonia mydas)
<p>Relocations from 25 green turtles, tracked in West Africa in 2021.</p>
Evidence from the Literature to Answer Specific Research Questions
<p>All the relevant information that was extracted from the 21 selected articles to answer the four specific research questions (SRQ1, SRQ2, SRQ3, and SRQ4) are presented in a form of a complete table.</p>
Evidence from the Literature to Answer Specific Research Questions
<p>All the relevant information that was extracted from the 21 selected articles to answer the four specific research questions (SRQ1, SRQ2, SRQ3, and SRQ4) are presented in a form of a complete table.</p>
FIGURE 2 in Molecular investigation of the intra-specific genetic variation in Plantago ovata Forssk. (Plantaginaceae): An insight into potential ancestral area distribution and probable time of dispersal versus vicariance events
FIGURE 2 Combined RASP and chronological tree of BEAST for P. ovata accessions (The scale numbers are in MY).
FIGURE1 in Molecular investigation of the intra-specific genetic variation in Plantago ovata Forssk. (Plantaginaceae): An insight into potential ancestral area distribution and probable time of dispersal versus vicariance events
FIGURE1 TCS network of the studied P. ovata plants based on ITS sequences showing a higher level of nucleotide replacement within the Asiatic samples (Hatch marks indicate the number of mutations).
Data of Publication "Theoretical rheo-physics of silk: Intermolecular associations reduce the critical specific work for flow-induced crystallization"
<p>Data of Publication:</p> <p><em>Theoretical rheo-physics of silk: Intermolecular associations reduce the critical specific work for flow-induced crystallization<br> Charley Schaefer and Tom C. B. McLeish<br> Citation: Journal of Rheology 66, 515 (2022); doi: 10.1122/8.0000411<br> View online: https://doi.org/10.1122/8.0000411</em></p>
Supplemental Data for Generalized Testing for Finite State Specifications
<p>Additional supplemental data for <em>Generalized Testing for Finite State Specifications</em>.</p> <p>Files in this dataset:<br> - `edge-pair-analysis.tgz` contains all data from analysis done in Section III-B (On the bugginess of mined specs).<br> - `preliminary-study-mined-fsms.tgz` contains all mined FSMs used for analysis in Section III-B (On the bugginess of mined specs).<br> - `temari-study-data.tgz` contains all Temari experiment data for RQ1 (How generalizable is Temari?).</p>
Patient-specific identification of genome-wide DNA-methylation differences between intracranial and extracranial melanoma metastases
<p>This is the data used in github repository: https://github.com/TheresaKraft/MethylationManuscript</p>
FIGURE 4. Specific characteristics from P in Platystele peruviana sp nov. (Orchidaceae), the smallest orchid from Peru
FIGURE 4. Specific characteristics from P. peruviana. Photos taken from the type (dry specimen) A. Front view of the complete flower showing the lip and the glenion. B. back view of the complete flower showing the connate portion of lateral sepals. C. View of the lip and the glenion. D. Photo of the roots from the type (fresh specimen).
Network Theme: Continuous blood processing for patient specific therapies - Dr Robert Barker (University of Kent)
<p>This video is the third talk from our Future Blood Testing Network Plus Launch that took place on the 23/11/2021.</p> <p>Network Theme: Continuous blood processing for patient specific therapies - Dr Robert Barker (University of Kent)</p> <p>Bio: Dr Robert Barker is an Associate Professor in Chemistry in the School of Physical Sciences, School Director of Public Engagement, project lead for the ‘Future Human’ Signature Research, University of Kent (UoK). He is a Royal Society Industrial Fellow and the PI of the trans-disciplinary EPSRC project Optimising Me Manufacturing Systems [EP/R022534/1], exploring continuous blood processing for healthcare and developing a healthcare micro-factory that provides on-the-body manufacturing of therapeutics, continuously and in response to the body’s needs. His work focuses on the whole blood processing and the development of a manufacturing system for T-cell immunotherapies which present a cure for some of the most aggressive forms of cancer (acute lymphoblastic leukaemia and chronic lymphoblastic leukaemia). His research is at the interface of industry and the NHS to meet their needs for continuous blood monitoring and to help the shift away from the current one-size-fits-all approach to deliver patient-specific therapies.</p> <p>Further details on this event can be found at: https://futurebloodtesting.org/event/23-11-21-future-blood-testing-network-launch/</p> <p>This video is an output from the Future Blood Testing Network which is funded by EPSRC under Grant Number EP/W000652/1</p> <p>YouTube Link: https://youtu.be/T4UVEOM1cZU</p>
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.