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13,017 results for “Positionning”
FIGURE 7 in Phylogenetic position of Kinnareemimus khonkaenensis (Dinosauria: Theropoda: Ornithomimosauria) from the Lower Cretaceous of Thailand
FIGURE 7. Comparison of proximal tibia in lateral view (line drawing) of Kinnareemimus (A), Tyrannomimus (B), Garudimimus (C), Beishanlong (D), and Deinocheirus (E). Comparison of fibula in proximal view (line drawing) of Kinnareemimus (F), Garudimimus (G), Deinocheirus (H), Sinornithomimus (I), and Gallimimus (J). Pedal unguals in lateral (K, M, O, Q) and ventral (L, N, P, R, S - V) views of (K, L) Nqwebasaurus (Choiniere et al. 2012), (M, N) Kinnareemimus (SM-PW5A-122), (O, P) Tyrannomimus (Hattori et al. 2023), (Q, R) Garudimimus (Kobayashi & Barsbold 2005b), (S) Deinocheirus (Lee et al. 2014), (T) cf. Qiupalong sp. (McFeeters et al. 2017), (U) Bissekty ornithomimid (Sues & Averianov 2016), and (V) Kazak Ornithomimid (Averianov et al. 2017). Not to scale.
FIGURE 5 in Phylogenetic position of Kinnareemimus khonkaenensis (Dinosauria: Theropoda: Ornithomimosauria) from the Lower Cretaceous of Thailand
FIGURE 5. Phylogenetic analyses (A) modified after Choiniere et al. (2012) and found Kinnareemimus within the Deinocheiridae, (B) modified after McFeeters et al. (2016) and found Kinnareemimus as a basal ornithomimosaur. Numbers next to nodes are Bremer support values.
FIGURE 2 in Phylogenetic position of Kinnareemimus khonkaenensis (Dinosauria: Theropoda: Ornithomimosauria) from the Lower Cretaceous of Thailand
FIGURE 2. Previous cladistic analyses from (A) Senter 2007, (B) Choiniere et al. 2012, (C) Lee et al. 2014, (D) McFeeters et al. 2017.
FIGURE 4 in Phylogenetic position of Kinnareemimus khonkaenensis (Dinosauria: Theropoda: Ornithomimosauria) from the Lower Cretaceous of Thailand
FIGURE 4. Left metatarsals of Kinnareemimus in proximal (A, C, G, N), anterior (B, D, E, I, J), posterior (H, L), and distal (F, K, M) views. Incomplete left metatarsal III SM-PW5A-100 (E-H), mid shaft of the left metatarsal III SM-PW5A-103 (I, L, M), and distal portion of the left metatarsal III SM-PW5A-107 (J, K, N). Cross section of metatarsal III SM-PW5A-100 (G), SM-PW5A-103 (M), and SM-PW5A-107 (N). Abbreviation: bif: bifurcation of posterior ridge; elp: extensor ligament pit; nap: nonarticular platform; prid: posterior ridge; arrowhead = medial expansion. Scale bar = 5 cm.
FIGURE 3 in Phylogenetic position of Kinnareemimus khonkaenensis (Dinosauria: Theropoda: Ornithomimosauria) from the Lower Cretaceous of Thailand
FIGURE 3. Left tibia of Kinnareemimus in anterior (A, B), posterior (C), medial (D), lateral (E, F), proximal (G, H), and distal (I, J) views. Left fibula of Kinnareemimus in proximal (K) and lateral (L) views. Abbreviations: cc, cnemial crest; fc, fibular crest; ig, intercondylar groove; it, incisura tibialis; lc, lateral condyle; lm, lateral malleolus; mc, medial condyle; mm, medial malleolus. Scale bar = 10 cm.
FIGURE 6 in Phylogenetic position of Kinnareemimus khonkaenensis (Dinosauria: Theropoda: Ornithomimosauria) from the Lower Cretaceous of Thailand
FIGURE 6. Phylogenetic analysis modified after Hattori et al. (2023) and found Kinnareemimus as a basal ornithomimosaur.
FIGURE 8 in Phylogenetic position of Kinnareemimus khonkaenensis (Dinosauria: Theropoda: Ornithomimosauria) from the Lower Cretaceous of Thailand
FIGURE 8. Simplified cladogram showing morphological diversity of ornithomimosaur metatarsals (left metatarsals II, III, IV in proximal and anterior views). Nqwebasaurus (modified from Choiniere et al. 2012; Sereno 2017); Harpymimus (modified from Kobayashi & Barsbold 2005a); Kinnareemimus (modified from Buffetaut et al. 2009); Beishanlong (modified from Makovicky et al. 2010); Garudimimus (modified from Kobayashi & Barsbold 2005b); Deinocheirus (modified from Lee et al. 2014); Ornithomimus velox (modified from Claessens & Loewen 2015); arcto = arctometatarsus; pre-sub = pre-subarctometatarsus; sub = subarctometatarsus; DEINO = Deinocheiridae; * = Ornithomimoidea (according to Sereno 2017) or Macrocheiriformes (according to Cuesta et al. 2021).
Figure 7. A in Re-evaluation of the systematic position of the order Prostomatida (Protista: Ciliophora), with the establishment of two new genera and two new species
Figure 7. A, putative secondary structure of V9 region of small subunit ribosomal RNA (SSU rRNA) gene of 18 representative species. The major differences are indicated by shading. B, the unique sites of the alignment of SSU rRNA gene sequences for the two groups. Group 1 contains Prostomatida and Trimyemidae; group 2 contains Apsiktratidae and some representative prorodontids.
Figure 3 in Re-evaluation of the systematic position of the order Prostomatida (Protista: Ciliophora), with the establishment of two new genera and two new species
Figure 3. Platina marina gen. nov., sp. nov. from life (A–L), after protargol staining (M, O–R) and after 4ʹ,6-diamidino-2-phenylindole (DAPI) staining (N). A, ventral view of a representative individual, showing general appearance of body. B, the caudal cilium (arrow). C, H, I, lateral view, showing shape variants and transverse bulge located on dorsal side (arrowheads). D–G, ventral view, showing shape variants. J, K, compressed individuals, showing the silverline system of the ventral side (arrows) and dorsal side (arrowheads), and perioral cilia (double arrowheads). L, silverline system of the dorsal side. M, N, showing the macronucleus and micronucleus (arrow). O, ciliary pattern of the anterior portion of the cell, showing the circumoral kinety (arrowhead) and perioral kineties (arrow). P, the dividing line between the ventral side and the dorsal side, showing the only transverse row of kinetids on the dorsal side (arrowhead). Q, R, side view of the holotype specimen, showing ciliary pattern of the cell, circumoral kinety (arrowheads) and the only transverse row of kinetids on the dorsal side (arrow) except for perioral kineties. Scale bars: 25 μm in A–I; 10 μm in Q, R.
Figure 6 in Re-evaluation of the systematic position of the order Prostomatida (Protista: Ciliophora), with the establishment of two new genera and two new species
Figure 6. Maximum likelihood (ML) tree inferred from small subunit ribosomal RNA (SSU rRNA) gene sequences, showing the phylogenetic positions of the three newly sequenced species (bold font). Numbers near the nodes represent the ML bootstrap values and Bayesian inference (BI) posterior probabilities, respectively. Fully supported (100/1.00) branches are marked with filled circles. Asterisks (*) indicate disagreements between the ML and BI trees. The scale bar corresponds to five substitutions per 100 nucleotide positions.
Figure 2 in Re-evaluation of the systematic position of the order Prostomatida (Protista: Ciliophora), with the establishment of two new genera and two new species
Figure 2. Platina marina gen. nov., sp. nov. from life (A, F, G) and after protargol staining (B–E, H). A, ventral view of a representative individual, showing general appearance of body. B, C, dorsal (C) and ventral (B) side view of the holotype specimen, showing ciliary pattern of the cell, circumoral kinety (arrows) and the gap (arrowhead) in circumoral kinety. D, ciliary pattern of the anterior portion of the cell, showing the circumoral kinety (CK), perioral kineties (PK) and the only transverse row of kinetids on the dorsal side (arrowhead). E, showing the dividing line (arrow) between ventral side and dorsal side. F, lateral view (a) and ventral side view (b) of the same specimen, showing dorsoventrally flattened body and transverse bulge located on the dorsal side (arrowhead). G, silverline system of dorsal side. H, silverline system of ventral side. I, a schematic diagram of an apical view of the cell, showing the circumoral kinety (double arrowhead), perioral kineties (arrowheads) and the only transverse row of kinetids on the dorsal side (arrow). Scale bars: 15 μm.
Figure 1 in Re-evaluation of the systematic position of the order Prostomatida (Protista: Ciliophora), with the establishment of two new genera and two new species
Figure 1. Maps showing the location and photographs showing the appearance of the sampling sites. A, location of Qingdao and sampling sites. B, photograph of intertidal area near Zhanqiao Pier where Parametacystis pulchra gen. nov., sp. nov. and Platina marina gen. nov., sp. nov. were collected. C, photograph of a small pond in Taipingjiao Park where Apsiktrata gracilis was collected. S, salinity; T, temperature.
Figure 4 in Re-evaluation of the systematic position of the order Prostomatida (Protista: Ciliophora), with the establishment of two new genera and two new species
Figure 4. Drawing (A–E) and photomicrographs (F–L) of Parametacystis pulchra gen. nov., sp. nov. from life (A, D, F–H) and after protargol staining (B, C, E, I–L). A, lateral view of a representative individual, showing general appearance of body and protruding caudal vacuole (arrow). B, C, side view of the holotype specimen, showing ciliary pattern of the cell and circumoral kinety (arrowheads). D, showing the pattern of the silverline system and cortical granules. E, ciliary pattern of the anterior portion of the cell, showing the circumoral kinety (CK) and the perioral kineties (PK). F, showing the protruding caudal vacuole (arrow). G, lateral view of a slightly contracted individual, showing the furrows in ectoplasm (arrowheads). H, compressed individual, showing the pattern of the silverline system and cortical granules (arrows). I, lateral view of holotype specimen, showing ciliary pattern and macronucleus (Ma). J, showing the macronucleus and micronucleus (arrow). K, L, showing the circumoral kinety (arrowheads) and perioral kineties (arrows). Scale bars: 20 μm.
ECMWF IFS potential salinity and temperature data interpolated to ALAMO float positions. Results of tropical cyclone tracking algorithm for TC Irma, Florence, Teddy and Ida simulations with ECMWF IFS.
<p>ECMWF IFS potential salinity and temperature data interpolated to ALAMO float positions. The data is from forecasts of tropical cyclone Irma, Florence, Teddy and Ida performed at horizontal atmosphere resolutions of TCo1279, TCo2559, TCo3999, TCo7999 and ocean resolutions of eORCA025 and eORCA025.</p> <p> </p> <p>Data also contains the results of tracking these tropical cyclones in the ECMWF IFS simulations. </p>
Data from: Evolutionary patterns of ploidy and genome size variations show positive correlations with taxonomic diversity in tropical gingers (Zingiberaceae)
<p><strong>Premise: </strong>Cytogenetic traits such as an organism's chromosome number and genome size are taxonomically critical and can define angiosperm diversity. Variations in these cytogenetic traits by evolutionary processes such as polyploidization are known to be common, although underexplored in tropical plants. Zingiberaceae is a pantropical monocot family with ~1500 species where cytogenetic characters have often been used to define taxonomic boundaries, but a family-wide synthesis of cytogenetic patterns is absent.</p> <p><strong>Methods:</strong> A time-calibrated Bayesian phylogenetic tree was constructed to test for different models of chromosome number and genome size evolution in Zingiberaceae. We next tested how chromosome number and genome size variations differed with lineage-age, taxonomic diversity, and distributional range at two taxonomic ranks: within the family Zingiberaceae, and in the genus Hedychium using correlations, generalized linear models and phylogenetic least square models.</p> <p><strong>Key results:</strong> The most frequent changes in chromosome number within Zingiberaceae were demi-polyploidization and polyploidization (~57 % of the time), followed by ascending dysploidy (~27 %). The subfamily Zingiberoideae showed descending dysploidy at its base, while Alpinioideae showed polyploidization at its internal nodes. Although chromosome counts and genome sizes did not corroborate with each other, suggesting that they are not equivalent, at both taxonomic ranks, higher chromosome number variations and higher genome size variations were associated with higher taxonomic diversity and wider biogeographic distribution.</p> <p><strong>Conclusions:</strong> Within Zingiberaceae, multiple incidences of polyploidization were discovered, and these cytogenetic events appear to have impacted the morphology, decreased genome sizes, and increased taxonomic diversity, distributional range and invasiveness of plants within this family. </p>
Women's status in Higher leadership positions in Ethiopia since 1991
<p>Gender equality in decision-making positions is crucial to achieving the goals of good governance, peace, democracy, and inclusive/sustainable development. The major aim of this research article is to investigate the representation trend of women in higher decision-making positions over the last thirty years, since 1991. The federal three organs of government (law formulating, law enforcing, and law interpreting bodies) were the focus of this research. This research is a mixed type of research that inculcates both qualitative and quantitative data types. Secondary data sources from relevant government institutions were mostly used. The data analyzed through content analysis of documents and presented via descriptive data presenting techniques. The result of this research disclosed the underrepresentation of women's in Ethiopian federal higher leadership positions across the last three decades, despite today's some advancement of women's involvement in decision-making positions. Furthermore, Women never held certain higher-level leadership positions, such as the Prime Minister position, which seems to be forbidden for women. Women made up 23%, 19%, 19%, and 24% of the legislature, the House of Federation (HoF), ministerial posts, and judicial bodies, respectively. Women are visibly underrepresented in the Ethiopian executive body as compared to others. Thus, substantial policy and practical initiatives are needed to remove institutional, social, and economic barriers to boost women's advanced visibility in senior leadership roles.</p>
Replication package for: An Analysis of Positionality Statements in Software Engineering Research
Open the record for dataset details and reuse information.
Indoor Positioning - de Blasio et al - dataset paper IEEE Access (2018)
<p>This zip file contains the raw BLE data in .xlsx format obtained in the tests detailed in the following article (attached pdf):</p> <p>Gabriel de Blasio, Alexis Quesada-Arencibia, Carmelo R. García, José Carlos Rodríguez-Rodríguez, Roberto Moreno-Díaz jr. A Protocol-Channel-Based Indoor Positioning Performance Study for Bluetooth Low Energy, IEEE Access vol. 6, pp. 33440-33450 (2018)<br>DOI: 10.1109/ACCESS.2018.2837497</p>
Indoor Positioning - de Blasio et al - dataset paper Sensors (2019)
<p>This zip file contains the raw BLE data in .xlsx format obtained in the tests detailed in the following article (attached pdf):</p> <p>de Blasio, Gabriele Salvatore, Rodríguez-Rodríguez, José C., Garcia, Carmelo R., Quesada-Arencibia, Alexis. Beacon-related parameters of bluetooth low energy: development of a semi-automatic system to study their impact on indoor positioning systems, Sensors vol. 19(4), (2019) DOI: 10.3390/s19143087</p>
Effects of M-components on needle activity in positive cloud-to-ground lightning flashes
<p>The data supports the manuscript entitled “Effects of M-components on needle activity in positive cloud-to-ground lightning flashes”. The high-speed video data files of the positive cloud-to-ground lightning lighnting (F20064 and F20065) of *.avi can be opened by Photron Camera Control software (Photron Fastcam Viewer) that can be download from this link: https://photron.com/photron-support/</p> <p>In addition, MATLAB can open the *.mat file (electric field change data), and Microsoft Excel can open the *.xlsx file (Guangdong-Hong Kong-Macao Lightning Location data (F20064 & F20065).</p> <p>The data can be used freely for scientific purposes with the appropriate citation.</p>
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.