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Text-fig. 5. East-west cross section of the Urema Graben and Cheringoma Plateau adapted from Pfaffhuber et al. (2009). The Urema Graben is ca. 45–50 km broad. Note that in this scheme, the Eocene Limestone (i.e., the Cheringoma Fm) is overlain by Oligocene sandstone in the position mapped as Mazamba Formation by Real (1966) and by Tinley (1977). in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 5. East-west cross section of the Urema Graben and Cheringoma Plateau adapted from Pfaffhuber et al. (2009). The Urema Graben is ca. 45–50 km broad. Note that in this scheme, the Eocene Limestone (i.e., the Cheringoma Fm) is overlain by Oligocene sandstone in the position mapped as Mazamba Formation by Real (1966) and by Tinley (1977).
Text-fig. 4. Type specimens of Magnolia allasoniae MARTINETTO sp. nov. from the Pliocene locality Ca' Viettone. a1–a4: Holotype (MGPT-PU141081) in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 5) in a black and white print (a1), in a new digital photograph in basal view (a2), ventral view (a3) and dorsal view (a4); b1–b4: Paratype MGPT-PU141082 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 4) in a black and white print (b1), in a new digital photograph in basal view (b2), ventral view (b3) and dorsal view (b4); c1–c4: Paratype MGPT-PU141083 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 6) in a black and white print (c1), in a new digital photograph in basal view (c2), ventral view (c3) and dorsal view (c4); d1–d4: Paratype MGPT-PU141084 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 7) in a black and white print (d1), in a new digital photograph in basal view (d2), ventral view (d3) and internal view (d4). Scale bars 1 mm. in Late Messinian Flora From The Post-Evaporitic Deposits Of The Piedmont Basin (Northwest Italy)
Text-fig. 4. Type specimens of Magnolia allasoniae MARTINETTO sp. nov. from the Pliocene locality Ca' Viettone. a1–a4: Holotype (MGPT-PU141081) in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 5) in a black and white print (a1), in a new digital photograph in basal view (a2), ventral view (a3) and dorsal view (a4); b1–b4: Paratype MGPT-PU141082 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 4) in a black and white print (b1), in a new digital photograph in basal view (b2), ventral view (b3) and dorsal view (b4); c1–c4: Paratype MGPT-PU141083 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 6) in a black and white print (c1), in a new digital photograph in basal view (c2), ventral view (c3) and dorsal view (c4); d1–d4: Paratype MGPT-PU141084 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 7) in a black and white print (d1), in a new digital photograph in basal view (d2), ventral view (d3) and internal view (d4). Scale bars 1 mm.
Supplementary information for the paper about foreign authors in russian journals (2000-2021, ca 600 journals)
<p>This is a supplementary dataset for the article about foreign authors in Russian Scopus-indexed journals (in Russian). It contains publication and citation data for countries, journals, country clusters, subject areas and topics</p> <p>Based on the set of ca.90000 papers with strictly foreign affiliations (without Russian affiliations) in ca 600 journals for 2000-2021</p>
In-situ XANES data for the calcination of Ca(II)/Ce(IV)-doped LaPO4 monazite
<p>These files include raw data from high temperature in-situ HERFD-XANES measurements at the ROBL beamline at the ESRF as well as laboratory PXRD data of the solid solution La1-xCax/2Cex/2PO4 produced by co-precipitation and a solid state route. All necessary background information will be found in the journal article this data will be linked to.</p>
Dataset: Xtrackers California Municipal Bond ETF (CA) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Fig. 4 in M Or P Ho L O Gi Ca L Va R Iati On An D P Op U Lat Io N Structure Of The Natterjack Toad, Epidalea Calamita, In Northern Part Of The Range In Belarus
Fig. 4. Variation of the ratios males and females in the Natterjack toad Epidalea calamita population during the activity season in Belarus.
Fig. 3 in M Or P Ho L O Gi Ca L Va R Iati On An D P Op U Lat Io N Structure Of The Natterjack Toad, Epidalea Calamita, In Northern Part Of The Range In Belarus
Fig. 3. The color differences of males and females Natterjack toad Epidalea calamita in population of Belarus.
Fig. 3 in M Or P Ho L O Gi Ca L Va R Iati On An D P Op U Lat Io N Structure Of The Natterjack Toad, Epidalea Calamita, In Northern Part Of The Range In Belarus
Fig. 3. The color differences of males and females Natterjack toad Epidalea calamita in population of Belarus.
Рис. 2. Варианты преΑсказанной Αоменной структуры патогенраспознающих моΛекуΛ гемоцитов моΛΛюсков Planorbarius corneus. a — фибриногенпоΑобные беΛки, b — гаΛектины, c — F-Λектины. УсΛовные обозначения и сокращения, зΑесь и ΑаΛее: горизонтаΛьные красные поΛоски — сигнаΛьный пептиΑ, горизонтаΛьные розовые — обΛасть низкой сΛожности, вертикаΛьные синие поΛоски — трансмембранная обΛасть, FBG — фибриногеновый Αомен, FTP — Αомен фукоΛектина, EGF — Αомен эпиΑермаΛьного фактора роста, EGF_CA — каΛьцийсвязывающий EGF-поΑобный Αомен, PAN_AP — APPLE-поΑобный Αомен, SCAN — обΛасть, богатая Λейцином, GLECT — гаΛактозосвязывающий Λектин, CLECT — Λектин C-типа, Gal-bind — гаΛактозиΑ–связывающий Λектин, ML — MD-2- поΑробный Αомен распознавания ΛипиΑов Fig. 2. Variants of the predicted domain structure of pattern recognition molecules from hemocytes of Planorbarius corneus molluscs. a — fibrinogen-related proteins, b — galectins, c — F-lectins. Symbols and abbreviations (here and further): horizontal red stripes — signal peptide, horizontal pink stripes — a low complexity region, vertical blue stripes — transmembrane region, FBG — fibrinogen-related domain, FTP — fucolectin domain, EGF — epidermal growth factor-like domain, EGF_CA — calcium-binding EGF-like domain, PAN_AP — APPLE-like domain, SCAN — leucine rich region, Apple — APPLE domain, GLECT — galactose-binding lectin, CLECT — C-type lectin, Gal-bind — galactoside-binding lectin, ML — MD-2-related lipid-recognition domain in Pathogen recognition molecules from hemocytes of Planorbarius corneus molluscs (Planorbidae, Pulmonata)
Рис. 2. Варианты преΑсказанной Αоменной структуры патогенраспознающих моΛекуΛ гемоцитов моΛΛюсков Planorbarius corneus. a — фибриногенпоΑобные беΛки, b — гаΛектины, c — F-Λектины. УсΛовные обозначения и сокращения, зΑесь и ΑаΛее: горизонтаΛьные красные поΛоски — сигнаΛьный пептиΑ, горизонтаΛьные розовые — обΛасть низкой сΛожности, вертикаΛьные синие поΛоски — трансмембранная обΛасть, FBG — фибриногеновый Αомен, FTP — Αомен фукоΛектина, EGF — Αомен эпиΑермаΛьного фактора роста, EGF_CA — каΛьцийсвязывающий EGF-поΑобный Αомен, PAN_AP — APPLE-поΑобный Αомен, SCAN — обΛасть, богатая Λейцином, GLECT — гаΛактозосвязывающий Λектин, CLECT — Λектин C-типа, Gal-bind — гаΛактозиΑ–связывающий Λектин, ML — MD-2- поΑробный Αомен распознавания ΛипиΑов Fig. 2. Variants of the predicted domain structure of pattern recognition molecules from hemocytes of Planorbarius corneus molluscs. a — fibrinogen-related proteins, b — galectins, c — F-lectins. Symbols and abbreviations (here and further): horizontal red stripes — signal peptide, horizontal pink stripes — a low complexity region, vertical blue stripes — transmembrane region, FBG — fibrinogen-related domain, FTP — fucolectin domain, EGF — epidermal growth factor-like domain, EGF_CA — calcium-binding EGF-like domain, PAN_AP — APPLE-like domain, SCAN — leucine rich region, Apple — APPLE domain, GLECT — galactose-binding lectin, CLECT — C-type lectin, Gal-bind — galactoside-binding lectin, ML — MD-2-related lipid-recognition domain
Amber Lipid17 Simulations of POPC/POPS Membranes with Ca+2 Counterions
<p><strong>System: </strong>Simulations of POPC/POPS (5:1, 144 lipids in total) membranes with Ca+2 counterions</p> <p><strong>Number of POPS:</strong> 24.</p> <p><strong>Number of POPC</strong> 120.</p> <p><strong>Number of waters:</strong> 5760.</p> <p><strong>Number of Ions: </strong>12.</p> <p><strong>Lipid model:</strong> Amber Lipid 17 [IR Gould, AA Skjevik, CJ Dickson, BD Madej, RC Walker: "Lipid17: A Comprehensive AMBER Force Field for the Simulation of Zwitterionic and Anionic Lipids" in prep. (2018)].</p> <p><strong>Ion models: </strong> Li/Merz Ions [Li, P. <em>J. Chem. Theory Comput.</em> <strong>9</strong> 2733-2748 (2013)].</p> <p><strong>Water model:</strong> TIP3P [WL Jorgensen, J Chandrasekhar, JD Madura, RW Impey, ML Klein <em>J. Chem. Phys.</em> <strong>79</strong> 926 (1983)].</p> <p><strong>Simulation engine:</strong> Amber16 [DA Case et al. <em>AMBER 2017</em> UCSF (2017)].</p> <p><strong>Number of independent repeats per setup: </strong>2.<br> <strong>Trajectory lengths per repeat:</strong> 200 ns.<br> <strong>Previously equilibrated for:</strong> 100 ns.<br> <strong>Sampling rate:</strong> every 10 ps.</p> <p><strong>Time integration step:</strong> 2 fs.</p> <p><strong>Thermodynamic ensemble:</strong> NpT. <br> <strong>Temperature coupling:</strong> 'Langevin' at T = 298 K.<br> <strong>Pressure coupling: '</strong>Berendsen' [<em>J. Chem. Phys.</em> <strong>81</strong> 3684 (1984); <em>J. Chem. Phys.</em> <strong>103</strong> 10252 (1995)] with xy and z coupled separately at p = 1.0 bar with no surface tension.</p> <p><strong>Electrostatics: </strong>PME [<em>J. Chem. Phys.</em> <strong>98</strong> 10089 (1993);<em> J. Chem. Theory Comput.</em> <strong>9</strong> 3878 (2013)].<br> <strong>Van der Waals:</strong> Turned off between 1.0 nm and 1.5 nm.</p> <p><strong>Constraints: </strong>Lengths of covalent bonds involving Hydrogens in lipids using SHAKE [<em>J. Comput. Phys.</em> <strong>23</strong> 327 (1977)], in water using SETTLE [<em>J. Comput. Chem. </em><strong>13</strong> 952 (1992)].</p> <p><strong>Used in publications: </strong>OHS Ollila et al. "NMRlipids IV: Headgroup & glycerol backbone structures, and cation binding in bilayers with PS lipids" in prep (2018).</p>
Stable Water Isotope Surveys - Muskoka River Watershed ON CA 2015-16
<p>This dataset includes river stable water isotope surveys from the Muskoka River watershed ON CA, conducted from April 2015 through November 2016. Ten river survey sites and one headwater stream site are included with listed site ID, sample date and ratios of oxygen and hydrogen isotope ratios. Data includes location of river survey sites and additional source water sampling sites (precipitation, snowmelt, groundwater). Daily average streamflow records for the 2015-2016 period of surveys originally sourced from the Water Survey of Canada website are included here (but can also be downloaded independently) for four of the six gauging stations referenced with the river survey isotope dataset. Water Survey of Canada gauging station locations are also provided.</p>
Fig. 1 in Evaluation of Intracellular Ca Concentration by Fura 2 Ratiometry in Encystment-induced Colpoda cucullus
Fig. 1. The elevation in the intracellular Ca2+ concentration (F /F 340 380 ratio) in encystment-induced C. cucullus. F340 and F380 are the fluorescence intensities of fura 2 excited at 340-nm and 380-nm light, respectively. The cells loaded with fura 2-AM were suspended in 1 mM Tris-HCl buffer (pH 7.2) containing 0.1 mM CaCl2 (open circles), the same buffer without addition of CaCl2 (closed squares or closed circles), and the same buffer containing 10 µM EGTA (open squares) at high (50,000 cells/ml) ('H') or low (2,000 cells/ ml) ('L') cell density. Open triangles show the F340/F380 ratios of the cells suspended in 1 mM Tris-HCl buffer (pH 7.2) without addition of 0.1 mM CaCl2 at a low cell density (2,000 cells/ml) together with a high-density (48,000 particles/ml) PLP (26 µm in diameter, Sigma-Aldrich) ('L/PLP'). Points and attached bars correspond to the means of 5 identical measurements and standard errors.
Text-fig. 5. CA climate charts for the Monte Tondo and Tossignano floras, showing climatic ranges of the Nearest Living Relatives of the fossil taxa with respect to MPwarm. For legend see Text-fig. 3. in Palaeoenvironmental Analysis Of The Messinian Macrofossil Floras Of Tossignano And Monte Tondo (Vena Del Gesso Basin, Romagna Apennines, Northern Italy)
Text-fig. 5. CA climate charts for the Monte Tondo and Tossignano floras, showing climatic ranges of the Nearest Living Relatives of the fossil taxa with respect to MPwarm. For legend see Text-fig. 3.
Text-fig. 4. CA climate charts for the Monte Tondo and Tossignano floras, showing climatic ranges of the Nearest Living Relatives of the fossil taxa with respect to MAP. For legend see Text-fig. 3. in Palaeoenvironmental Analysis Of The Messinian Macrofossil Floras Of Tossignano And Monte Tondo (Vena Del Gesso Basin, Romagna Apennines, Northern Italy)
Text-fig. 4. CA climate charts for the Monte Tondo and Tossignano floras, showing climatic ranges of the Nearest Living Relatives of the fossil taxa with respect to MAP. For legend see Text-fig. 3.
Text-fig. 3. CA climate charts for the Monte Tondo and Tossignano floras, showing climatic ranges of the Nearest Living Relatives of the fossil taxa with respect to MAT. Right-hand positoned large bold figures and shaded areas in each case indicate the Coexistence Interval, with the number of overlapping taxa being at a maximum. in Palaeoenvironmental Analysis Of The Messinian Macrofossil Floras Of Tossignano And Monte Tondo (Vena Del Gesso Basin, Romagna Apennines, Northern Italy)
Text-fig. 3. CA climate charts for the Monte Tondo and Tossignano floras, showing climatic ranges of the Nearest Living Relatives of the fossil taxa with respect to MAT. Right-hand positoned large bold figures and shaded areas in each case indicate the Coexistence Interval, with the number of overlapping taxa being at a maximum.
Text-fig. 1. D&E tree of Endress and Doyle (2009), from the combined morphological and molecular analysis of Doyle and Endress (2000), with modifications based on more recent data, showing the inferred evolution of the reticulum grading character (39). Boxes under names of taxa indicate their character state; shading of branches indicates their reconstructed state based on parsimony optimization with MacClade (Maddison and Maddison 2003). Nymph = Nymphaeales, Aust = Austrobaileyales, Chlor = Chloranthaceae, Piper = Piperales, Ca = Canellales, Magnol = Magnoliales. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 1. D&E tree of Endress and Doyle (2009), from the combined morphological and molecular analysis of Doyle and Endress (2000), with modifications based on more recent data, showing the inferred evolution of the reticulum grading character (39). Boxes under names of taxa indicate their character state; shading of branches indicates their reconstructed state based on parsimony optimization with MacClade (Maddison and Maddison 2003). Nymph = Nymphaeales, Aust = Austrobaileyales, Chlor = Chloranthaceae, Piper = Piperales, Ca = Canellales, Magnol = Magnoliales.
Fig. 5 in Two New Species of Japanese Earthworms (Annelida, Oligochaeta, Megadrilacea, Megascolecidae) Update Biodiversity on Okinawa and at Lake Biwa to ca. 30 Species
Fig. 5. Metaphire kinki sp. nov. P2 specimen (photo courtesy Kazuhiro Masunaga March, 2011 with LBM permission via M.J. Grygier pers. comm. 22nd July, 2015).
Fig. 4 in Early evolution of Coriariaceae (Cucurbitales) in light of a new early Campanian (ca. 82 Mya) pollen record from Antarctica
Fig. 4. The evolution of chromosome numbers in Coriaria inferred under a best-fitting maximum-likelihood model (Materials and Methods).
Fig. 1 in Early evolution of Coriariaceae (Cucurbitales) in light of a new early Campanian (ca. 82 Mya) pollen record from Antarctica
Fig. 1. Distribution map of Coriaria species generated from georeferenced data available in GBIF (accessed Jan 2019).
Fig. 2 in Early evolution of Coriariaceae (Cucurbitales) in light of a new early Campanian (ca. 82 Mya) pollen record from Antarctica
Fig. 2. Selected extant and fossil species of Coriaria. A, C. myrtifolia (photo by Tanja M. Schuster); B, Holotype of C. longaeva G. de Saporta, 1866, showing the characteristic venation pattern, leaf attachment, and terminal inflorescence; C, C. sarmentosa flowers showing protogyny (photo by Pieter Pelser, PhytoImages, Nickrent & al., 2006 –); D, Fruits of C. sarmentosa with accrescent corollas (photo by Tanja M. Schuster); E, The characteristically small leaves of C. microphylla or C. ruscifolia subsp. microphylla (photo by Axel Dalberg Poulsen); F, C. ruscifolia in Chile (photo by Mark Olson).
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.