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157 results for “F2”
Seasonal high-frequency measurements of discharge, water temperature, and specific conductivity from Huey Creek at F2, McMurdo Dry Valleys, Antarctica (1990-2023, ongoing)
As part of the Long Term Ecological Research (LTER) project in the McMurdo Dry Valleys of Antarctica, a systematic sampling program has been undertaken to monitor the glacial meltwater streams in that region. This package contain data pertaining to continuous monitored water quality and quantity parameters measured with automatic recording devices on streams in this region. Specifically, this metadata record describes the hydrology data set for the McMurdo Dry Valleys' Huey Stream at the F2 streamgage, located in the Fryxell Basin of Taylor Valley. Measurements commenced during the 1990-91 season. The Huey at F2 control was buried by sediment and rock sometime before 29 Dec 2010 and the site was abandoned on 19 Jan 2011. An upstream location was established 28 Dec 2012. This dataset extends through the first half of the 2022-23 field season.
Daily summarized seasonal measurements of discharge, water temperature, and specific conductivity from Huey Creek at F2, McMurdo Dry Valleys, Antarctica (1990-2023, ongoing)
As part of the Long Term Ecological Research (LTER) project in the McMurdo Dry Valleys of Antarctica, a systematic sampling program has been undertaken to monitor the glacial meltwater streams in that region. This package contains daily summaries derived from 15-minute measurements of water quality and quantity parameters measured with automatic recording devices on streams in this region. Specifically, this metadata record describes the daily hydrological summaries for the McMurdo Dry Valley's Huey Creek at F2, located in the Fryxell Basin of Taylor Valley. Measurements commenced during the 1990-91 austral summer and are ongoing. This dataset extends through the first half of the 2019-20 field season. The Huey at F2 control was buried by sediment and rock sometime before 29 Dec 2010 and the site was abandoned on 19 Jan 2011. An upstream location was established 28 Dec 2012. This dataset extends through the first half of the 2022-23 field season.
The datasets used in the manuscript named "Dynamical Seasonal Prediction of Tropical Cyclone Activity Using a Global Ensemble Prediction System FGOALS-f2 V1.0"
<p>The hindcast and real-time prediction output of FGOALS-f2 V1.0 used in the study named "Dynamical Seasonal Prediction of Tropical Cyclone Activity Using a Global Ensemble Prediction System FGOALS-f2 V1.0"</p>
Quartet of familiar females – 16p11.2 Del mouse strain – 2 WT + 2 Del/+ - F2
<p>We monitored the individual and social behaviours of each quartet of mice over three days and nights in the Live Mouse Tracker system (LMT, plugin 931; de Chaumont et al. 2019 Nat. Biomed. Engin.). This system tracks individually mice living in a group over several days and nights and extracts automatically the number, total duration and mean duration of more than thirty behavioural events describing the posture of the mouse, the types of social contacts, the dynamic social approach and escapes and complex social groupings (see de Chaumont et al. 2019 Nat. Biomed. Engin.). In this system, the four mice (10-14 weeks of age; 2 WT mice and 2 Del/+ mice) from the same housing cage (housed together from weaning on) were left undisturbed for 71 hours in a large transparent Plexiglas cage (50 x 50 x 40 cm), with fresh bedding, a house (width: 100 mm, depth: 75 mm, height: 40 mm) in red Plexiglas, 6 dental cotton rolls as well as food and water ad libitum. Light/dark cycle and temperature conditions were similar to those of the housing room (12/12h light/dark, lights on at 07:00 AM, 100 lux when the lights were on). Each recording session started between 03:00 and 04:00 PM. At the end of the session, mice were placed back in their home cage and the LMT setup was cleaned with soap water and dried with paper towels. The upload includes the sqlite database from LMT (processed).</p>
Tibial apophysis slightly curved outward as seen from below (F1); embolus twisted with deep indentation, appearing bifid (F2) in An of Zelotibia (Araneae, Gnaphosidae), a spider genus with a species swarm in the Albertine Rift
Tibial apophysis slightly curved outward as seen from below (F1); embolus twisted with deep indentation, appearing bifid (F2)
Text-fig. 4. Paludocyon bohemicus (SCHLOSSER, 1899), from Tuchořice, the Czech Republic, lower teeth. a: NM-Pv 11677, left m1 (lectotype), a1 – buccal view, a2 – lingual view, a3 – occlusal view; b: NM-Pv 11700, left mandible with c, alveoli for p1–p2, and p3–m2, b1 – occlusal view, b2 – lingual view, b3 – buccal view; c: NM-Pv 11695, right mandible with p2–m2, c1 – lingual view, c2 – buccal view, c3 – occlusal view; d: NM-Pv 11698, right p4–m2, d1 – lingual view, d2 – occlusal view, d3 – buccal view; e: NM-Pv 11697, right p3–m3, e1 – occlusal view, e2 – lingual view; f: NM-Pv 11699, left mandible with p3–m3, f1 – lingual view, f2 – occlusal view, f3 – buccal view; g: NM-Pv 11722, left p4–m3, g1 – buccal view, g2 – lingual view, g3 – occlusal view. in The Amphicyoninae (Amphicyonidae, Carnivora, Mammalia) Of The Early Miocene From Tuchořice, The Czech Republic
Text-fig. 4. Paludocyon bohemicus (SCHLOSSER, 1899), from Tuchořice, the Czech Republic, lower teeth. a: NM-Pv 11677, left m1 (lectotype), a1 – buccal view, a2 – lingual view, a3 – occlusal view; b: NM-Pv 11700, left mandible with c, alveoli for p1–p2, and p3–m2, b1 – occlusal view, b2 – lingual view, b3 – buccal view; c: NM-Pv 11695, right mandible with p2–m2, c1 – lingual view, c2 – buccal view, c3 – occlusal view; d: NM-Pv 11698, right p4–m2, d1 – lingual view, d2 – occlusal view, d3 – buccal view; e: NM-Pv 11697, right p3–m3, e1 – occlusal view, e2 – lingual view; f: NM-Pv 11699, left mandible with p3–m3, f1 – lingual view, f2 – occlusal view, f3 – buccal view; g: NM-Pv 11722, left p4–m3, g1 – buccal view, g2 – lingual view, g3 – occlusal view.
Text-fig. 6. Megamphicyon carnutense (ANTUNES et GINSBURG, 1977), from Tuchořice, the Czech Republic, lower teeth. a: NMPv 11708, left p4, a1 – occlusal view, a2 – buccal view, a3 – lingual view; b: NM-Pv 11709, left p4, b1 – occlusal view, b2 – buccal view, b3 – lingual view; c: NM-Pv 11710, left m1, c1 – lingual view, c2 – occlusal view, c3 – buccal view; d: NM-Pv 11711, left m1, d1 – lingual view, d2 – occlusal view, d3 – buccal view; e: NM-Pv 11747, left m1–m3, e1 – occlusal view, e2 – lingual view, e3 – buccal view; f: NM-Pv 11713, left m2, f1 – lingual view, f2 – occlusal view, f3 – buccal view; g: NM-Pv 11714, left m2, g1 – lingual view, g2 – occlusal view, g3 – buccal view; h: NM-Pv 11718, right m2, h1 – lingual view, h2 – occlusal view, h3 – buccal view, h4 – distal view; i: NM-Pv 11716, left m2 in occlusal view; j: NM-Pv 11717, left m2, j1 – occlusal view, j2 – buccal view; k: NMPv 11696, right m2–m3, k1 – lingual view, k2 – buccal view, k3 – occlusal view. in The Amphicyoninae (Amphicyonidae, Carnivora, Mammalia) Of The Early Miocene From Tuchořice, The Czech Republic
Text-fig. 6. Megamphicyon carnutense (ANTUNES et GINSBURG, 1977), from Tuchořice, the Czech Republic, lower teeth. a: NMPv 11708, left p4, a1 – occlusal view, a2 – buccal view, a3 – lingual view; b: NM-Pv 11709, left p4, b1 – occlusal view, b2 – buccal view, b3 – lingual view; c: NM-Pv 11710, left m1, c1 – lingual view, c2 – occlusal view, c3 – buccal view; d: NM-Pv 11711, left m1, d1 – lingual view, d2 – occlusal view, d3 – buccal view; e: NM-Pv 11747, left m1–m3, e1 – occlusal view, e2 – lingual view, e3 – buccal view; f: NM-Pv 11713, left m2, f1 – lingual view, f2 – occlusal view, f3 – buccal view; g: NM-Pv 11714, left m2, g1 – lingual view, g2 – occlusal view, g3 – buccal view; h: NM-Pv 11718, right m2, h1 – lingual view, h2 – occlusal view, h3 – buccal view, h4 – distal view; i: NM-Pv 11716, left m2 in occlusal view; j: NM-Pv 11717, left m2, j1 – occlusal view, j2 – buccal view; k: NMPv 11696, right m2–m3, k1 – lingual view, k2 – buccal view, k3 – occlusal view.
Text-fig. 3. Outcrop cross section of the turbidite facies distribution in the Majalengka, correlated northwest to southeast. The progradation pattern indicated by thickening of sandstone into the basin area are shown. F1 – heterolithic sandstone-mudstone 1; F2 – heterolithic sandstone-mudstone 2; F3 – mudstone facies; F4 – heterolithic fine sand and mudstone; F5 – conglomeratic to massive sandstone facies (Muljana 2012). in Lithofacies And Ichnofacies Of Turbidite Deposits, West Java, Indonesia
Text-fig. 3. Outcrop cross section of the turbidite facies distribution in the Majalengka, correlated northwest to southeast. The progradation pattern indicated by thickening of sandstone into the basin area are shown. F1 – heterolithic sandstone-mudstone 1; F2 – heterolithic sandstone-mudstone 2; F3 – mudstone facies; F4 – heterolithic fine sand and mudstone; F5 – conglomeratic to massive sandstone facies (Muljana 2012).
Figure 10 Optimal matrices for functions f1 (a), f2 (b), and f3 (c)-SELECTING OPERATIONS FOR ASSEMBLER ENCODING
<p>In the experiments, the following sets of operations were tested (a description of all<br> the operations specified below is presented in Appendix 1):<br> • Set 1 (all four-parameter operations used during the research reported in [15,17]):<br> CHG, CHGC0, CHGC1, CHGC2, CHGC3, CHGC4, CHGR0, CHGR1,<br> CHGR2, CHGR3, CHGR4, CHGM0, CHGM1, CHGM2, JMP;<br> • Set 2 (the most effective four-parameter operations used in the previous research):<br> CHGC0, CHGC3, CHGR0, CHGR3, CHGM0, CHGM2, JMP;<br> • Set 3: simpler variants of operations included in Set 1, the simpler operations, unlike<br> their more complex counterparts, always changed either the whole column or the<br> whole row or the whole matrix, operations from this set had maximally three<br> parameters;<br> • Set 4 (the three-parameter operations and jumps): CHG_VALUE, CHG_MEMORY,<br> JMP.</p>
FRACTESUS_VTT_15Kh2MFAA_F2_report
<div>Fractesus project. Fracture test mini-CT. Raw data 15Kh2MFAA. VTT. </div> <div> <div> <p> </p> </div> </div>
FRACTESUS_UoB_SA508_KJc_MCT_-100_F2
<div>Fractesus project. Fracture test mini-CT. Raw data SA508 Cl.3. UoB. </div>
Fig. 6. Electrophoresis agarose gel showing RFLP pattern comparison between the F2 in Detection of maize bushy stunt phytoplasma in leafoppers collected in native corn crops grown at high elevations in southeast Mexico
Fig. 6. Electrophoresis agarose gel showing RFLP pattern comparison between the F2nR2 sequences amplified from Dalbulus elimatus and Idiodonus wickhami digested with AluI, BstUI, HaeIII, HinfI, and Tsp509I. Molecular weight (MW) marker, 1 kb plus.
Text-fig. 11. Lower teeth of Masillamys mattaueri (HARTENBERGER) from Mas de Gimel (Hérault, France; MP 10, late early Eocene). a) MGL 641, left p4; a1 – occlusal view, a2 – buccal aspect, a3 – lingual aspect. b) MGL 220, right p4; b1 – occlusal view, b2 – buccal aspect, b3 – lingual aspect. c) MGL 233, right m1; c1 – occlusal view, c2 – buccal aspect, c3 – lingual aspect. d) MGL 665, right m1; d1 – occlusal view, d2 – buccal aspect, d3 – lingual aspect. e) MGL 225, holotype, right m2; e1 – occlusal view, e2 – buccal aspect, e3 – lingual aspect. f) MGL 222, left m1; f1 – lingual aspect, f2 – occlusal view, f3 – buccal aspect. g) MGL 231, right m2; g1 – occlusal view, g2 – buccal aspect, g3 – lingual aspect. h) MGL 646, left m3; h1 – buccal aspect, h2 – lingual aspect, h3 – occlusal view. i) MGL 619, right m3; i1 – buccal aspect, i2 – lingual aspect, i3 – occlusal view. Scale bar 1 mm. in A Reevaluation Of The Taxonomic Status Of The Rodent Masillamys Tobien, 1954 From Messel (Germany, Late Early To Early Middle Eocene, 48-47 M.Y.)
Text-fig. 11. Lower teeth of Masillamys mattaueri (HARTENBERGER) from Mas de Gimel (Hérault, France; MP 10, late early Eocene). a) MGL 641, left p4; a1 – occlusal view, a2 – buccal aspect, a3 – lingual aspect. b) MGL 220, right p4; b1 – occlusal view, b2 – buccal aspect, b3 – lingual aspect. c) MGL 233, right m1; c1 – occlusal view, c2 – buccal aspect, c3 – lingual aspect. d) MGL 665, right m1; d1 – occlusal view, d2 – buccal aspect, d3 – lingual aspect. e) MGL 225, holotype, right m2; e1 – occlusal view, e2 – buccal aspect, e3 – lingual aspect. f) MGL 222, left m1; f1 – lingual aspect, f2 – occlusal view, f3 – buccal aspect. g) MGL 231, right m2; g1 – occlusal view, g2 – buccal aspect, g3 – lingual aspect. h) MGL 646, left m3; h1 – buccal aspect, h2 – lingual aspect, h3 – occlusal view. i) MGL 619, right m3; i1 – buccal aspect, i2 – lingual aspect, i3 – occlusal view. Scale bar 1 mm.
Text-fig. 7. Teeth of Masillamys parvus TOBIEN, from Messel (Hesse, Germany, MP 11), HLMD-Me 625, holotype. a) left upper M2, protocone damaged, occlusal view. b) left upper M3, occlusal view. c) left lower p4; c1 – occlusal view, c2 – buccal aspect, c3 – lingual aspect. d) left lower m2, metaconid damaged; d1 – occlusal view, d2 – buccal aspect, d3 – lingual aspect. e) right m3, occlusal view. f) left m3; f1 – occlusal view, f2 – buccal aspect, base of crown lacking, f3 – lingual aspect; g) SMF-ME 2099A: right lower tooth row with dp4 to m3, g1 – occlusal view, g2 – lingual aspect. Scale bar 1 mm. in A Reevaluation Of The Taxonomic Status Of The Rodent Masillamys Tobien, 1954 From Messel (Germany, Late Early To Early Middle Eocene, 48-47 M.Y.)
Text-fig. 7. Teeth of Masillamys parvus TOBIEN, from Messel (Hesse, Germany, MP 11), HLMD-Me 625, holotype. a) left upper M2, protocone damaged, occlusal view. b) left upper M3, occlusal view. c) left lower p4; c1 – occlusal view, c2 – buccal aspect, c3 – lingual aspect. d) left lower m2, metaconid damaged; d1 – occlusal view, d2 – buccal aspect, d3 – lingual aspect. e) right m3, occlusal view. f) left m3; f1 – occlusal view, f2 – buccal aspect, base of crown lacking, f3 – lingual aspect; g) SMF-ME 2099A: right lower tooth row with dp4 to m3, g1 – occlusal view, g2 – lingual aspect. Scale bar 1 mm.
Project F2 - Discovering Potential Market for the Integration of Public Transportation and Emerging Shared-Mobility Services
<p>This dataset compiles the results of ridesharing trajectory data aggregation, the analysis result of the transit and ridesharing trip data, and raw data of transit station coordinates and schedules in Chengdu, China. This is part of STRIDE project F2 titled "Discovering Potential Market for the Integration of Public Transportation and Emerging Shared-Mobility Services."</p>
Nämforsen, Laxön F2, Ådals Liden 193:1
Nämforsen, Laxön, Hallström_F2, Ådals Liden 193:1, Ångermanland. For more information see www.namforsen.com and www.shfa.se Source: Objaverse 1.0 / Sketchfab
Nämforsen, Notön F2, Ådals-Liden 193.
Nämforsen, Notön, Hallström_F2, Ådals-Liden 193, Ångermanland. For more information see www.namforsen.com and www.shfa.se Source: Objaverse 1.0 / Sketchfab
Nämforsen, Brådön F2, Ådals-Liden 193:1
Nämforsen, Brådön, Hallström_F2, Ådals-Liden 193:1. Ångermanland. For more information see www.namforsen.com and www.shfa.se Source: Objaverse 1.0 / Sketchfab
SNP data for F2 population derived from Oryza rufipogon and O. nivara
<p>To elucidate the genetic architecture underlying phenotypic divergence is essential to the understanding of ecological adaptation and speciation. Two wild rice species (<em>O. rufipogon</em> and <em>O. nivara</em>) are a progenitor-daughter species pair with ecological divergence and provide a unique system for studying ecological adaptation/speciation. Here, we constructed a high-resolved linkage map and conducted a quantitative trait locus (QTL) analysis of 19 phenotypic traits using an F<sub>2</sub> population generated from a cross between the perennial <em>O. rufipogon</em> and annual <em>O. nivara</em>. We identified 113 QTLs associated with interspecific divergence of 16 quantitative traits, with effect sizes ranging from 1.61% to 34.1% in terms of the percentage of variation explained (PVE). The distribution of effect sizes of QTLs followed a negative exponential, suggesting that a few genes of large effect and many genes of small effect were responsible for the phenotypic divergence. We observed 18 clusters of QTLs (QTL hotspots), with each involving multiple adaptive traits, demonstrating the importance of coinheritance of loci/genes in ecological adaptation/speciation. Analysis of effect direction and <em>v</em>-test statistics revealed that interspecific differentiation of most traits was driven by divergent natural selection, supporting the argument that ecological adaptation/speciation would proceed rapidly under coordinated selection on multiple traits.</p>
Figure 101. Acrotelsella aff. marginata F2 in On some silverfish taxa from the Cape York region of northern Australia (Zygentoma: Lepismatidae: Ctenolepismatinae)
Figure 101. Acrotelsella aff. marginata F2 from Punsand Bay campground, Queensland.
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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)
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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.
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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.