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12,237 results for “2019”
Fig. 4 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 4. Photomicrographs of reproductive stages of female O. circumpicta. (A) early developing, (B) late developing, (C) ripe, (D) partially spawned, (E) spent/absorbing, (F) resting.
Fig. 5 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 5. Photomicrographs of reproductive stages of male O. circumpicta. (A) early developing, (B) late developing, (C) ripe, (D) partially spawned, (E) spent/absorbing, (F) resting.
Fig. 3 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 3. Monthly variations in the surface water temperature, salinity and chlorophyll a at the sampling location from September 2003 to September 2004. The sea surface temperature and salinity data were obtained from Korea Hydrographic and Oceanographic Agency, and the chlorophyll a were referred from NASA EARTHDATA (https:// earthdata.nasa.gov/, USA)
Fig. 5 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 5. Lynceus amplopedia sp. nov., male, scanning electron microscopy (paratype NMHD-615845). A, head, anterior view (left antenna removed); B, head, anteroventral view, left antenna removed; C, head, right lateral view; D, rostral apex, left lateral view; E, left mandible, lateral view; F, left first antennae; G, telson with opercular lamella, ventral view. H, right clasper, anterior view; I, left clasper, posterior view, encircled areas with scales; J, setae (magnification of I); K, clasper gripping area with setae, apical view; L, large palp (e5), right clasper, dorsal view; M, clasper palm (e3) with scales (upper encircled area in I), lateral view; N, setae and scales of clasper gripping area (magnification of I). Abbreviations: e3–e5 = endites 3–5.
Fig. 5 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 5. Planotergum kowalevski sp. nov., holotype female (8.6 × 11.7 mm) (ZMMU Ma 3506), Red Sea: a, front of carapace, eye and antenna, dorsal view; b, antenna, dorsal view; c, antenna, ventral view; d, ventral view of P2; e, left third maxilliped; f, ventral view of P2. Scale bars = 1.0 mm.
Fig. 4 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 4. Planotergum kowalevski sp. nov., holotype female (8.6 × 11.7 mm) (ZMMU Ma 3506), Red Sea: a, ventral view of chelipeds and third maxillipeds; b and c, eyes; d, front of carapace, dorsal view; e, thoracic sternites; f, ventral view of ambulatory appendages (P2–5); g, P2; h, chelipeds. Scale bars = 3.0 mm
Fig. 2 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 2. Species composition and percentage of eels collected from the Fengshan River. The bar charts in white represent A. japonica, and those in gray represent A. marmorata. The numbers in every bar chart are the total number of captured eels.
Fig. 1 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 1. Map of the sampling sites in the Fengshan River of Taiwan. The Fengshan River is located in northwestern Taiwan, East Asia. FS1 and FS2 are in the lower reaches, FS3 and FS4 are in the middle reaches, and FS5 and FS6 are in the upper reaches of the Fengshan River. This figure was drawn by using Adobe Illustrator CS6 (Adobe Systems Incorporated, USA).
Fig. 3 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 3. Planotergum kowalevski sp. nov., holotype female (8.6 × 11.7 mm) (ZMMU Ma 3506), Red Sea: a and b, general dorsal view; c, ventral view; d, lateral view. Scale bars = 5.0 mm.
Fig. 2. Planotergum mirabile Balss, 1935. a, c, d, g–n in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 2. Planotergum mirabile Balss, 1935. a, c, d, g–n, female (7.7 × 10.1 mm) (ZRC 1985.130), Singapore; b, e, f, female (10.2 × 13.4 mm) (ZRC 1969.11.19.12), Java Sea: a and b, general dorsal view; c, left third maxilliped; d, right antenna (ventral view, dorsal covered by bryozoan); e, right antenna (dorsal view); f, left eye; g, i, l, n, P2–5 (dorsal views, setae intact); h, j, k, m, o, P2–5 (ventral views, setae denuded); k, P2, ventral view.
Fig. 1 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 1. Map of localities where representatives of the genus Planotergum Balss, 1935 have been reported.
Fig. 3 in Ophiacantha scissionis Lee & Stöhr & Bae & Shin 2019, sp. nov.
Fig. 3. Relative mRNA expression of sMYH, fMYH, dio2, gria3, s100b and neurod1 in the glass eels of A. japonica and A. marmorata. The mRNA expression levels were presented as mean ± SD. The asterisk (*) shows that the mRNA expression levels between A. japonica and A. marmorata were significantly different (p <0.05). N = 10 for each eel species.
Рис. 1. ФиΛогенетические Αеревья хантавируса AMRV и его прироΑного носитеΛя восточноазиатской мыши Apodemus peninsulae Thomas, 1906. А. ФиΛогенетическое Αерево восточноазиатской мыши Apodemus peninsulae, построенное метоΑом «максимаΛьного правΑопоΑобия» (ML) и поΛученное на основе анаΛиза участка гена цитохрома b мтΔНК (744 п.н.). В узΛах ветвΛения указаны бутстреп-поΑΑержки, рассчитанные ΑΛя 1000 повторов. Цветными Λиниями обозначены фиΛогенетические Λинии: Αве Китайские (зеΛеный), Корейская «Korea» (синий), Амурская «Amur» (красный). ПоΛужирным шрифтом выΑеΛены собственные образцы. Названия образцов из GenBank/NCBI быΛи сокращены; B. ФиΛогенетическое Αерево из работы Α. Н. Яшиной с ΑопоΛнениями, построенное метоΑом «бΛижайшего сосеΑа» (NJ) на основе посΛеΑоватеΛьностей фрагмента М-сегмента (2737–2980 н.п.) генома хантавирусов. В узΛах ветвΛения указаны бутстреппоΑΑержки, рассчитанные ΑΛя 1000 повторов. Жирным выΑеΛены иссΛеΑованные РНК изоΛяты (Яшина 2012; Яшина и Αр. 2019) Fig. 1. Phylogenetic trees of AMRV and its natural reservoir host — the Korean field mouse Apodemus peninsulae Thomas, 1906. A. Phylogenetic tree of the Korean field mouse Apodemus peninsulae constructed by the "maximum likelihood" method (ML). The data are obtained from the analysis of the cytochrome b mtDNA gene fragments (744 bp). Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. Colored lines indicate phylogenetic lines: two Chinese (green), Korea (blue), and Amur (red). Own samples are highlighted in bold. The names of the samples from GenBank/NCBI have been shortened; B. Phylogenetic tree from L. N. Yashina's work with additions constructed by the neighbour joining method (NJ). It is based on the sequences of an M-segment fragment (2737–2980 bp) of the hantavirus genome. Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. The researched RNA isolates are highlighted in bold (Yashina 2012; Yashina et al. 2019) in Variability of the gene cyt b in the Korean field mouse Apodemus peninsulae Thomas, 1906 - a reservoir host of AMRV in the Khasansky District of Primorsky Krai
Рис. 1. ФиΛогенетические Αеревья хантавируса AMRV и его прироΑного носитеΛя восточноазиатской мыши Apodemus peninsulae Thomas, 1906. А. ФиΛогенетическое Αерево восточноазиатской мыши Apodemus peninsulae, построенное метоΑом «максимаΛьного правΑопоΑобия» (ML) и поΛученное на основе анаΛиза участка гена цитохрома b мтΔНК (744 п.н.). В узΛах ветвΛения указаны бутстреп-поΑΑержки, рассчитанные ΑΛя 1000 повторов. Цветными Λиниями обозначены фиΛогенетические Λинии: Αве Китайские (зеΛеный), Корейская «Korea» (синий), Амурская «Amur» (красный). ПоΛужирным шрифтом выΑеΛены собственные образцы. Названия образцов из GenBank/NCBI быΛи сокращены; B. ФиΛогенетическое Αерево из работы Α. Н. Яшиной с ΑопоΛнениями, построенное метоΑом «бΛижайшего сосеΑа» (NJ) на основе посΛеΑоватеΛьностей фрагмента М-сегмента (2737–2980 н.п.) генома хантавирусов. В узΛах ветвΛения указаны бутстреппоΑΑержки, рассчитанные ΑΛя 1000 повторов. Жирным выΑеΛены иссΛеΑованные РНК изоΛяты (Яшина 2012; Яшина и Αр. 2019) Fig. 1. Phylogenetic trees of AMRV and its natural reservoir host — the Korean field mouse Apodemus peninsulae Thomas, 1906. A. Phylogenetic tree of the Korean field mouse Apodemus peninsulae constructed by the "maximum likelihood" method (ML). The data are obtained from the analysis of the cytochrome b mtDNA gene fragments (744 bp). Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. Colored lines indicate phylogenetic lines: two Chinese (green), Korea (blue), and Amur (red). Own samples are highlighted in bold. The names of the samples from GenBank/NCBI have been shortened; B. Phylogenetic tree from L. N. Yashina's work with additions constructed by the neighbour joining method (NJ). It is based on the sequences of an M-segment fragment (2737–2980 bp) of the hantavirus genome. Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. The researched RNA isolates are highlighted in bold (Yashina 2012; Yashina et al. 2019)
Geochemical and isotopic compositions of lake waters, creek and permafrost of Central Yakutia from 2017, 2018 and 2019
<p>The file contains a table of all data of geochemical and isotopic compositions of lake waters, creek and permafrost of Central Yakutia from 2017, 2018 and 2019.</p>
Fig. 1 in The first record of Rhabdocoela, Alcha sinensis, Wang & Hu, 2019 (Platyhelminthes: Polycystididae) from Korea
Fig. 1. Alcha sinensis Wang & Hu, 2019: (A) habitus from a live animal; (B, C) squeezed live specimen showing the characteristic bands of blue and yellow pigment; (D) ventral plate of stylet; (E & F) dorsal plate of stylet; (G) lamellar plate covering (D) and (F). Abbreviations used in the figures: e: eye; eg: (fertilized) egg; ma: male atrium; o: ovary; p: proboscis; ph: pharynx; st: stylet; sv: seminal vesicle; t: testis; vi: vitellarium. Scale bars; A-C: 100 μm, D-G: 20 μm).
CLDF dataset derived from Sawka et al.'s "Toka-Leya of Zambia" from 2019
<p>Cite the source of the dataset as:</p> <blockquote> <p>Sawka, Kenneth S. and Mbewe, Christopher and Josephat, Daka and Schwertfeger, Jacob (2019): Toka-Leya of Zambia: Southern Province: Livingstone, Kazungula, Zimba, and Kalomo District. SIL International.</p> </blockquote>
ICSE 2018 and ICPC 2019 Session Video Recordings
<p>Session recordings analyzed in two following research works:</p> <ul> <li>Title: <em>The Road to Live Programming: Insights From the Practice</em> <ul> <li>Authors: Juraj Kubelka, Romain Robbes, Alexandre Bergel</li> <li><a href="https://www.icse2018.org/event/icse-2018-technical-papers-the-road-to-live-programming-insights-from-the-practice">ICSE 2018</a></li> </ul> </li> <li>Title: <em>Live Programming and Software Evolution: Questions during a Programming Change Task</em> <ul> <li>Authors: Juraj Kubelka, Romain Robbes, Alexandre Bergel</li> <li><a href="https://conf.researchr.org/home/icpc-2019">ICPC 2019</a></li> </ul> </li> </ul> <p>The dataset includes the following audio and video recordings and the file names are composed of <session-id>-<participant-id>.</p> <p>Session Video Recordings [session id, participant id, spoken language]:</p> <ol> <li>S1-P1, Audio is excluded at the request of the participant</li> <li>S2-P2, English</li> <li>S3-P3, Spanish</li> <li>S4-P5, English</li> <li>S5-P8, Spanish</li> <li>S6-P9, Spanish</li> <li>S7-P11, English</li> <li>S8-P4, English</li> <li>S9-P5, Spanish</li> <li>S10-P6, English</li> <li>S11-P4, English</li> <li>S12-P5, Spanish</li> <li>S13-P6, English</li> <li>S14-P8, Spanish</li> <li>S15-P9, Spanish</li> <li>S16-P10, English</li> <li>S17-P11, English</li> </ol> <p>Participants who spoke Spanish during the session spoke their mother tongue. English-speaking participants use English as a second language.</p> <p> </p>
Summary data to support Hall (2019), '(e) in Normandy: The sociolinguistics, phonology and phonetics of the "Loi de Position"'
<p>Article abstract:</p> <p>This article uses the pronunciation of stressed Intonational Phrase-final /ε/ and /e/ in two communities in Normandy, France, to illustrate the convergence of two sociolinguistic processes on the same phonological result: increasing application of the <em>Loi de Position</em>. In both communities (one rural and further from Paris, one urban and closer to Paris), there is now no consistent community-wide phonetic distinction between the two phonemes in that environment. It is suggested that the <em>Loi de Position</em> is already widely applied in the rural site, but speakers are still conscious of the formal norm whereby it is not applied; for the urban site, apparent-time changes for this variable reflect changes in Parisian speech. The theoretical implications of the study concerning speakers’ organisation of their vowel-space, and concerning the increasing application of the <em>Loi de Position</em> in the French of France, are examined. These conclusions are reached by per-speaker analysis of F1 and F2 separately from each other (rare in French linguistics). As a measure of community cohesion, the article introduces to linguistics the coefficient of variation (more common in biology and medicine).</p>
JCDL 2019, ORKG, use case dataset
<p>DILS 2019 use-case dataset, collected via subject matter experts to represent DILS 2019 papers as a machine readable graph model</p>
Simulation results from HadGEM-UKCA perturbed parameter ensembles for Yoshioka et al. 2019 JAMES
<p>This dataset was created from perturbed parameter ensembles (PPEs) using HadGEM-UKCA atmospheric composition climate model and used in Yoshioka et al. (Ensembles of Global Climate Model Variants Designed for the Quantification and Constraint of Uncertainty in Aerosols and their Radiative Forcing) submitted to The Journal of Advances in Modeling Earth Systems (JAMES). It contains the following data;</p> <p>N50_sfc_data.tar.gz contains simulated number concentrations of particles larger than 50 nm from one-at-a-time screening experiments used in Figure 1 of the paper. teaca-teacl are job IDs of different experiments where values of parameters RAIN_FRAC and CLOUD_ICE_THRESH were varied;<br> teaca: RAIN_FRAC=0.6, CLOUD_ICE_THRESH=0.7<br> teacb: RAIN_FRAC=0.6, CLOUD_ICE_THRESH=0.5<br> teacc: RAIN_FRAC=0.6, CLOUD_ICE_THRESH=0.3<br> teacd: RAIN_FRAC=0.6, CLOUD_ICE_THRESH=0.1<br> teace: RAIN_FRAC=0.4, CLOUD_ICE_THRESH=0.7<br> teacf: RAIN_FRAC=0.4, CLOUD_ICE_THRESH=0.5<br> teacg: RAIN_FRAC=0.4, CLOUD_ICE_THRESH=0.3<br> teach: RAIN_FRAC=0.4, CLOUD_ICE_THRESH=0.1<br> teaci: RAIN_FRAC=0.2, CLOUD_ICE_THRESH=0.7<br> teacj: RAIN_FRAC=0.2, CLOUD_ICE_THRESH=0.5<br> teack: RAIN_FRAC=0.2, CLOUD_ICE_THRESH=0.3<br> teacl: RAIN_FRAC=0.2, CLOUD_ICE_THRESH=0.1</p> <p>CCN0p2_Stations_for_figure6.xlsx contains cloud condensation nuclei concentration at 0.2% supersaturation calculated for the AER ensemble of simulations at station locations used to create Figure 6 of the paper.</p> <p>Mean_Variance_CCN0p2_L9_AER_2008ANN.nc and Mean_Variance_CCN0p2_L9_AER-ATM_2006ANN.nc are emulator means and variances of annual average cloud condensation nuclei concentration at 0.2% supersaturation at model level 9 (~650m) in AER and AER-ATM ensembles and used in Figures 7 and 8.</p> <p>Mean_Variance_AOD550_AER_2008ANN.nc and Mean_Variance_AOD550_AER-ATM_2006ANN.nc are emulator means and variances of annual average aerosol optical depth at 550 nm in AER and AER-ATM ensembles and used in Figures 7 and 8.</p> <p>Mean_Variance_RFnet_AER_2008ANN.nc and Mean_Variance_ERF_AER-ATM_2006ANN.nc are emulator means and variances of annual average aerosol radiative forcing in AER ensemble and aerosol effective radiative forcing in AER_ATM ensemble and used in Figures 7, 8 and 9.</p> <p>Mean_Variance_SeaSalt_Load_AER_2008ANN.nc and Mean_Variance_SeaSalt_Load_AER-ATM_2006ANN.nc are emulator means and variances of annual average column mass loading of sea salt aerosol in AER and AER-ATM ensembles and used in Figure 9.</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.