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150 results for “TEMPO”
Figure 8 in Reappraisal and new material of the holotype of Draconyx loureiroi (Ornithischia: Iguanodontia) provide insights on the tempo and modo of evolution of thumb-spiked dinosaurs
Figure 8. Three dimensional models of the pes of Draconyx loureiroi holotype ML 357. Articulated pes (ML 357-12) (A–F) in medial (A), lateral (B), dorsal (C), plantar (D) and caudal (E) views, F, detail of metatarsal I. Abbreviations: as: astragalus, ca, calcalneum, fi: fibula, lm: lateral malleolus, mm: medial malleolus, mt-I: metatarsal I, mt-II: metatarsal II, mt-III: metatarsal III, mt-IV: metatarsal IV, p II-1: pedal phalanx II-1, p II-1: pedal phalanx II-2, p III-1: pedal phalanx III-1, p III-3: pedal phalanx III-3, ta-3: tarsal 3, ta-4: tarsal 4, un-II: ungual II, un-III: ungual III.
Figure 6 in Reappraisal and new material of the holotype of Draconyx loureiroi (Ornithischia: Iguanodontia) provide insights on the tempo and modo of evolution of thumb-spiked dinosaurs
Figure 6. Three dimensional models of limb bones elements of Draconyx loureiroi holotype ML 357 (ML 357 6-8), femur (A–E) and tibia and proximal end of fibula (F–J). Femur (ML 357 – 6) in cranial view (A), medial view (B), caudal view (C), lateral view (D) and distal view (E). Tibia (ML 357 – 7) and proximal end of fibula (ML 357 – 8) in cranial view (F), medial view (G), caudal view (H), lateral (I) and proximal (J) views.
Figure 1 in Reappraisal and new material of the holotype of Draconyx loureiroi (Ornithischia: Iguanodontia) provide insights on the tempo and modo of evolution of thumb-spiked dinosaurs
Figure 1. Geographical and geological settings of ML 357. A, B, Stratigraphic log of the Lourinhã Formation and position of the specimen. C, Re-adapted from Rotatori et al. (2020). Map of the Iberian Peninsula courtesy of Eduardo Puertolas-Pascual.
Figure 7 in Reappraisal and new material of the holotype of Draconyx loureiroi (Ornithischia: Iguanodontia) provide insights on the tempo and modo of evolution of thumb-spiked dinosaurs
Figure 7. Comparison of distal sections of femoral shaft from selected iguanodontians. A, Draconyx loureiroi, B, Uteodon aphanoecetes, C, Cumnoria prestwichii, D, Camptosaurus dispar, E, Barilium dawsoni, F, Mantellisaurus atherfieldensis and G, Iguanodon galvensis. Abbreviations: cod: condylid, eg: extensor groove, fg: flexor groove, lc: lateral condyle, mc: medial condyle. Distal sections drawn from: Carpenter & Wilson, 2008; Galton & Powell, 1980; Norman, 2011; Norman, 1986; Verdù et al., 2018.
Figure 2 in Reappraisal and new material of the holotype of Draconyx loureiroi (Ornithischia: Iguanodontia) provide insights on the tempo and modo of evolution of thumb-spiked dinosaurs
Figure 2. Two maxillary teeth of Draconyx loureiroi holotype ML 357 in labial and lingual views. Completely preserved maxillary in labial (A) and lingual (C) views; isolated maxillary crown in labial (B) and lingual (D) views. Abbreviations: ne: neck, os: occlusal surface, pr: primary ridge, tr: tertiary ridges.
Figure 4 in Reappraisal and new material of the holotype of Draconyx loureiroi (Ornithischia: Iguanodontia) provide insights on the tempo and modo of evolution of thumb-spiked dinosaurs
Figure 4. Three dimensional models of axial skeleton of Draconyx loureiroi holotype ML 357 (A–F): Caudal n.2 ML 357-10 in cranial view (A), left lateral view (B), caudal view (C), right lateral view (D), ventral view (E) and dorsal view (F). Caudal n.3 ML 357-11 (G–L) in cranial view (G), left lateral view (H), caudal view (I), right lateral view (J), ventral view (K) and dorsal view (L). Caudal n.1 ML 357-9 (M-R): cranial view (M), left lateral view (N), caudal view (O), right lateral view (P), ventral view (Q) and dorsal view (R). Abbreviations: cf: chevron facet, k: keel, nc: neural canal, ns: neural spine, tp: transverse process.
Figure 14 in Reappraisal and new material of the holotype of Draconyx loureiroi (Ornithischia: Iguanodontia) provide insights on the tempo and modo of evolution of thumb-spiked dinosaurs
Figure 14. Comparison of the manual anatomy of selected styracosternans. Uteodon aphanoecetes left manus (specimen CM 11337) in extensor view (A), proximal view (D) and palmar view (G). Camptosaurus dispar right manus, reversed (specimen USNM 4277) in extensor view (B), proximal view (E) and palmar view (H) (holotype USNM 4282). Magnamanus soriaensis right manus (holotype MNS 2000) in extensor view (C), proximal view (F) and palmar view (I). Note the difference in the structure of the carpus: Uteodon aphanoecetes presents a partially fused and not closely packed carpus, Camptosaurus dispar presents a partially fused but closely packed carpus while Magnamanus soriaensis presents the typical stout and fused element of Styracosterna. J, Stratigraphic distribution of these characters. Abbreviations: dc1: distal carpal 1, dc2: distal carpal 2, dc3: distal carpal 3, dc4: distal carpal4, dc5: distal carpal 5, in: intermedium, mc1: metacarpal 1, ra: radiale, ul: ulnare.
Figure 9 in Reappraisal and new material of the holotype of Draconyx loureiroi (Ornithischia: Iguanodontia) provide insights on the tempo and modo of evolution of thumb-spiked dinosaurs
Figure 9. Three dimensional models of the articulated leg (A–B) and pes (C–D) of Draconyx loureiroi holotype ML 357. Leg in medial view (A) and lateral view (B). Pes in medial (C) and lateral (D) views.
Percursos da etnografia digital no estudo com os Mebêngôkre (Kayapó) em tempos pandêmicos
<p>Neste trabalho descrevo brevemente os caminhos percorridos na minha pesquisa de <br>Mestrado sobre os “Processos de formação de novas categorias conceituais e as agências <br>linguísticas Mebêngôkre Kayapó”135. O estudo é formado por narrativas autobiográficas que <br>me situam no contexto da pesquisa e detalham as travessias que me conduziram ao estudo de <br>alguns aspectos da língua Mẽbêngôkre, amparada na antropologia linguística. Trata-se de um <br>estudo etnográfico que envolveu, diálogos com interlocutores Kayapó, diferentes fontes <br>bibliográficas e de leituras sobre línguas Jê. Assim, será descrito os atravessamentos da <br>pesquisa devido à chegada da pandemia e os percursos que o trabalho foi tomando. </p>
All structures for electronic coupling for TEMPO
<ol> <li>'all_263_structures' folder contains all 263 structures' xyz files.</li> <li> 'results_all_coup_casscf_ma_tzvp.csv' contains names of all the structures with correct active space obtained using CASSCF-GMH1.</li> <li> 'results_all_coup_casscf_ma_svp.csv' contains names of all the structures with correct active space obtained using CASSCF-GMH2.</li> <li>'tddft_basis_coupling.csv' contains names of the five randomly selected structures.</li> </ol>
The tempo of greening in the European Alps: Spatial variations on a common theme
<p>The long-term increase of satellite-based proxies of vegetation cover is a well-documented response of seasonally snow-covered ecosystems to climate warming. However, observed greening trends are far from being uniform and substantial uncertainty remains concerning the underlying causes of this spatial variability. Here, we processed surface reflectance of the moderate resolution imaging spectroradiometer (MODIS) to investigate trends and drivers of changes in the annual peak values of the Normalized Difference Vegetation Index (NDVI). Our study focuses on the above treeline ecosystems in the European Alps. The NDVI changes of these ecosystems are highly sensitive to land cover and biomass changes and are marginally affected by anthropogenic disturbances. We found a widespread greening for the period 2000-2020, a pattern that is consistent with the overall increase of summer temperature. At the local scale, the spatial variability of greening was mainly due to the preferential response of north-facing slopes between 1900 m and 2400 m. Using high resolution imagery, we noticed that the presence of screes and outcrops locally magnified this response. At the regional scale, we identified hotspots of greening where vegetation cover is sparser than expected given the elevation and exposure. Most of these hotspots experienced delayed snowmelt and green-up dates in recent years. We conclude that the ongoing greening in the Alps primarily reflects the high responsiveness of sparsely vegetated ecosystems that are able to benefit the most from temperature and water-related habitat amelioration above treeline.</p>
Data from: Mosaic evolution of the skull in labrid fishes involves differences in both tempo and mode of morphological change
<p>Modularity is a ubiquitous feature of organismal design that plays an important role in structuring patterns of morphological diversification. Modularity can facilitate evolutionary changes by allowing subsets of traits to coevolve as integrated units and follow quasi-independent evolutionary trajectories, a pattern that may be particularly consequential in the case of highly complex morphological structures. Here we examine modularity in a complex and highly kinetic structure, the teleost skull, and ask if a modular organization of the skull has influenced the diversification dynamics of the shapes of its osteological components across the labrid phylogeny. We compiled one of the largest three-dimensional morphological datasets of fishes to date, and used geometric morphometrics to quantify patterns of cranial shape evolution across 184 species of wrasses (Labridae). We then tested several hypotheses of modularity inspired by functional and developmental relationships between cranial bones and compared phenotypic rates among modules. We also compared the fit of models of trait evolution for the entire skull and the various articulated bones that it comprises. Our analyses indicated strong support for a two-module hypothesis, one that encompasses the oral and pharyngeal jaws, and another module comprised of the neurocranium, hyoid apparatus and operculum. This functional hypothesis yielded one of the highest significant rate differentials across modules, yet we also found that the best-fitting models of trait evolution differed among skull bones. These results suggest that modularity can influence morphological diversification in complex biological structures via differences in both the tempo and mode of evolutionary change.</p>
HER-TEMPO - Real World Treatment-related Outcomes on T-DXd in Canada
ClinicalTrials.gov study NCT06386263. IPD Sharing: YES. Countries: 1. Publications: 1.
Funfitness Program With Music Tempo on Perceived Exertion, Flexibility, Balance and Cognition in Gym Going Females
ClinicalTrials.gov study NCT06985797. IPD Sharing: NO. Countries: 1. Publications: 9.
Low-dose Maximal-intent Versus Controlled-tempo Resistance Training on Quality-of-life in Older Adults
ClinicalTrials.gov study NCT06124911. IPD Sharing: NO. Countries: 1. Publications: 1.
Efficacy of a Timolol Nasal Spray as a Treatment for Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT) - (TEMPO)
ClinicalTrials.gov study NCT02484716. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Low-dose Maximal-intent Versus Controlled-tempo Resistance Training on Quality-of-life in Adults
ClinicalTrials.gov study NCT06107855. IPD Sharing: NO. Countries: 1. Publications: 2.
Data from: Journeys through discrete-character morphospace: synthesising phylogeny, tempo, and disparity
Open the record for dataset details and reuse information.
Data from: Tempo and mode of performance evolution across multiple independent origins of adhesive toe pads in lizards
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Data from: Early and Middle Triassic trends in diversity, evenness, and size of foraminifers on a carbonate platform in south China: Implications for tempo and mode of biotic recovery from the end-Permian mass extinction
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