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986 results for “Classicism”
Fig. 1 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach
Fig. 1. Present extension of Singapore's mangroves (in green). The numbers indicate the sites that were sampled during the 1-month Singapore Mangrove Insect Project (SMIP 2009); and the 2-year Mangrove Insect Project (MIP 2012-2014). 1, Mandai mangroves; 2, Kranji Nature Trail; 3, Sungei Buloh Wetland Reserve; 4, Lim Chu Kang; 5, Sarimbun mangroves; 6, Berlayer Creek; 7, Pulau Semakau original or old mangrove (SMO); 8, Pulau Semakau, replanted or new mangrove (SMN); 9, Changi creek; 10, Pulau Tekong; 11, Pulau Ubin, Chek Jawa; 12, Pasir Ris; 13, Pulau Seletar; 14, Sungei Cina.
Fig. 4 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach
Fig. 4. Thinophilus apicatus sp. nov., male. A, Detail of surstyli ventrally; B, Tips cerci dorsally; C, Ventral view of epandrium; D, Lateral view of epandrium.
Fig. 3 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach
Fig. 3. Thinophilus apicatus sp. nov., male. A, Mid femur; B, Hind femur; C, Posterior view of fore leg; D, Anterior view of fore coxa.
Source Data for the paper: "Quantum-classical simulations reveal the photoisomerization mechanism of a prototypical first-generation molecular motor"
<p>This dataset contains the raw data for the results shown in the paper.</p> <p>For each figure of the paper (main text), one directory with data file(s) is provided.</p>
Fig. 7 in Fractal analysis of ostracod shell variability: A comparison with geometric and classic morphometrics
Fig. 7. RW1/RW2 plot showing the neat separation of Krithe compressa from Krithe iniqua specimens. Deformation grids along RW1 (set at values of –0.2 and 0.2) are reported. A. Plot of RW1 against RW2 scores. B, C. Shell deformation at extreme values along RW1.
Fig. 4 in Fractal analysis of ostracod shell variability: A comparison with geometric and classic morphometrics
Fig. 4. Main morphological features of studied ostracods species. A. Krithe iniqua Abate, Barra, Aiello, and Bonaduce, 1993, right valve, transparence drawing from external view, sample 59, B.O.C. 2518, upper Pliocene, KI−29, sample 59. B. Krithe compressa (Seguenza, 1880), right valve, transparence drawing from external view, KC−29, sample 58, B.O.C. 2547, upper Pliocene.
Fig. 2 in Fractal analysis of ostracod shell variability: A comparison with geometric and classic morphometrics
Fig. 2. Krithe iniqua Abate, Barra, Aiello, and Bonaduce, 1993, right valves; transparence drawings from external view; sample 59; upper Pliocene. A. KI−01, B.O.C. 2490. B. KI−02, B.O.C. 2491. C. KI−03, B.O.C. 2492. D. KI−04, B.O.C. 2493. E. KI−05, B.O.C. 2494. F. KI−06, B.O.C. 2495. G. KI−07, B.O.C. 2496. H. KI−08, B.O.C. 2497. I. KI−09, B.O.C. 2498. J. KI−10, B.O.C. 2499. K. KI−11, B.O.C. 2500. I. KI−12, B.O.C. 2501. L. KI−13, B.O.C. 2502. M. KI−14, B.O.C. 2503. N. KI−15, B.O.C. 2504. O. KI−16, B.O.C. 2505. P. KI−17, B.O.C. 2506. Q. KI−18, B.O.C. 2507. R. KI−19, B.O.C. 2508. S. KI−20, B.O.C. 2509. T. KI−21, B.O.C. 2510. U. KI−22, B.O.C. 2511. V. KI−23, B.O.C. 2512. W. KI−24, B.O.C. 2513. Y. KI−25, B.O.C. 2514. Z. KI−26, B.O.C. 2515. AA. KI−27, B.O.C. 2516. BB. KI−28, B.O.C. 2517.
Fig. 9 in Fractal analysis of ostracod shell variability: A comparison with geometric and classic morphometrics
Fig. 9. Continuous shape variation in Krithe compressa valves drawn along RW 2. Deformation grids relate to specimen of the three different samples belonging to Krithe compressa from the highest (A) to the lowest (C) RW 2 scores (see Fig. 7). Deformation grid in B refers to undeformed shape. From the above, a valve from sample 58 (specimen KC 25), a specimen from sample 51 (KC 16), and a specimen from sample 50 (KC 1).
Fig. 5 in Fractal analysis of ostracod shell variability: A comparison with geometric and classic morphometrics
Fig. 5. The logarithm of number of pairs C of points with mutual distance smaller than R (̊m), as a function of log(R). Vertical dashed lines are the limits inside which the linear slope of log(C) on log(R) provides the best fitting to the data.
Fig. 1. A in Fractal analysis of ostracod shell variability: A comparison with geometric and classic morphometrics
Fig. 1. A. Ideal uniform network of 225 points spaced 2 mm apart over an area of 30 × 30 mm2. B. The log of number of pairs C of the stations, with mutual distance smaller than R, as a function of log(R) (mm); the vertical dashed lines represent the lower (4 mm) and upper (16 mm) limits of R, inside which the linear slope provides the best fitting to the investigated co−ordinates.
Fig. 8 in Fractal analysis of ostracod shell variability: A comparison with geometric and classic morphometrics
Fig. 8. This plot is the same as in Fig. 7, except for marks have been appended according to sample of provenance instead of species.
Fig. 3 in Fractal analysis of ostracod shell variability: A comparison with geometric and classic morphometrics
Fig. 3. Krithe compressa (Seguenza, 1880), right valves; transparence drawings from external view; sample 50 (A–G), sample 51 (H–R), sample 58 (S–BB); upper Pliocene. A. KC−01, B.O.C. 2519. B. KC−02, B.O.C. 2520. C. KC−03, B.O.C. 2521. D. KC−04, B.O.C. 2522.E. KC−05, B.O.C. 2523. F. KC−06, B.O.C. 2524. G. KC−07, B.O.C. 2525. H. KC−08, B.O.C. 2526. I. KC−09, B.O.C. 2527. J. KC−10, B.O.C. 2528. K. KC−11, B.O.C. 2529. L. KC−12, B.O.C. 2530. M. KC−13, B.O.C. 2531. N. KC−14, B.O.C. 2532. O. KC−15, B.O.C. 2533. P. KC−16, B.O.C. 2534. Q. KC−17, B.O.C. 2535. R. KC−18, B.O.C. 2536. S. KC−19, B.O.C. 2537. T. KC−20, B.O.C. 2538. U. KC−21, B.O.C. 2539. V. KC−22, B.O.C. 2540. W. KC−23, B.O.C. 2541. X. KC−24, B.O.C. 2542. Y. KC−25, B.O.C. 2543. Z. KC−26, B.O.C. 2544. AA. KC−27, B.O.C. 2545. BB. KC−28, B.O.C. 2546.
A boreal forest model benchmarking dataset for North America: a case study with the Canadian Land Surface Scheme including Biogeochemical Cycles (CLASSIC)
<p>A boreal forest model benchmarking dataset for North America by harmonizing eddy covariance and supporting measurements from black spruce (Picea mariana)-dominated mature forest stands.</p> <p>Dataset glossary and users’ instructions are documented in ‘README.md’. </p>
Hindustani Classical Music Transcription Dataset
<p>This dataset includes the transcriptions of Hindustani classical music recordings. Overall there are 430 pieces each having a 25-sec duration. These pieces include 329 Alap, 79 mid, and 22 end sections taken from 50 music recordings. Each transcription consists of annotations for Shrutis (22 in one octave) in 3 Shaptak (22 * 3 = 66), Alankar, and Silence or noise. We also include a symbol table mapping each annotation to a unique Unicode character.</p> <p> </p> <p>_________________________________________________________________________________________________________<br> This project was funded under grant number: ECR/2018/000204 by the Science & Engineering Research Board (SERB).</p>
Evidence for stronger sexual selection in males than females using an adapted method of Bateman's classic study of Drosophila melanogaster
<p>Bateman’s principle, originally a test of Darwin’s theoretical ideas, has since become fundamental to sexual selection theory and vital to contextualising the role of anisogamy and the operational sex ratio in sex differences in both reproductive competition and precopulatory sexual selection. Despite this, Bateman’s principle has received substantial criticism, and researchers have highlighted both statistical and methodological errors, suggesting that Bateman’s original experiment contains too much sampling bias for there to be any evidence of sexual selection. This study uses Bateman’s original method as a template, accounting for two fundamental flaws in his original experiments, (i) viability effects and (ii) a lack of mating behaviour observation. Experimental populations of <em>Drosophila melanogaster</em> consisted of wild-type focal individuals and non-focal individuals established by backcrossing the brown eye (<em>bw<sup>-</sup></em>) eye-colour marker. Mating assays included direct observation of mating behaviour and subsequently, total number of offspring were counted, to obtain measures of mating success, reproductive success, and standardised variance measures based on Bateman’s principle. The results provide observational support for Bateman’s principle, particularly that (i) males had significantly more variation in number of mates compared to females and (ii) males had significantly more individual variation in total number of offspring. We also find significantly steeper Bateman gradient for males compared to females, suggesting that sexual selection is operating more intensely in males. However, female remating was limited, providing the opportunity for future study to further explore female reproductive success in correlation with higher levels of remating.</p>
The Multidomain Sector and Its Relation to the Classical Sectors of the Regional Security Complex
<p>The Multidomain Sector and Its Relation to the Classical Sectors of the Regional Security Complex -model of multidomain sector</p> <p>The model was drafted as a part of research supported by Poland’s National Centre for Science under the grant entitled: The adaptation of the regional security complex in the face of climate change: the example of the Arctic, with number: UMO-2019/35/N/HS5/00578.</p>
Exact Thermodynamics and Transport in the Classical Sine-Gordon Model
<p>Raw data and Mathematica Notebook for the thermodynamics of the classical sine-Gordon model.</p> <p>It can be found:</p> <ol> <li>A transfer matrix code for equilibrium correlation functions.</li> <li>A solver for the classical Thermodynamic Bethe Ansatz and partitioning protocol.</li> <li>Monte Carlo data of the partitioning protocol.</li> </ol> <p> </p>
Data for: Simulated climate change causes asymmetric responses in insect life history timing potentially disrupting a classic ecological speciation system
<p>Climate change may alter phenology within populations with cascading consequences for community interactions and ongoing evolutionary processes. Here, we measured the response to climate change in two sympatric, recently diverged (~170 years) populations of <em>Rhagoletis</em> <em>pomonella</em> flies specialized on different host fruits (hawthorn and apple) and their parasitoid wasp communities. We tested whether warmer temperatures affect dormancy regulation and its consequences for synchrony across trophic levels and temporal isolation between divergent populations. Under warmer temperatures, both fly populations developed earlier. However, warming significantly increased the proportion of maladaptive pre-winter development in apple, but not hawthorn, flies. Parasitoid phenology was less affected, potentially generating ecological asynchrony. Observed shifts in fly phenology under warming may decrease temporal isolation, potentially limiting ongoing divergence. Our findings of complex sensitivity of life-history timing to changing temperatures predict that coming decades may see multifaceted ecological and evolutionary changes in temporal specialist communities.</p>
A Frontline Therapy Trial in Participants With Advanced Classical Hodgkin Lymphoma
ClinicalTrials.gov study NCT01712490. IPD Sharing: YES. Countries: 21. Publications: 9.
Tislelizumab in Participants With Relapsed or Refractory Classical Hodgkin Lymphoma
ClinicalTrials.gov study NCT04318080. IPD Sharing: YES. Countries: 2. Publications: 0.
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.