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54 results for “Deflection”
FIGURE 8 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 8. Male genitalia (A, B) (top—lateral view, middle—plan view, bottom—aedeagus extracted, lateral view) C. Female genitalia (top—lateral view; bottom—ventral view, detail) A. M. inducta n. sp., Peru, Lagunas Arrebiatadas, prep. genit. MUSA_015149 B. M. huamanii n. sp., Peru, Tres Ríos, prep. genit. MUSA_015150 C. M. prattorum udima n. ssp., Peru, La Florida, prep. genit. KF-1473
FIGURE 9 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 9. Female genitalia (top—lateral view; bottom—ventral view, detail) A. M. ronda n. sp., Peru, Laguna Salahuido, prep. genit. MUSA_015151 B. M. inducta n. sp., Peru, Lagunas Arrebiatadas, prep. genit. MUSA_015152
FIGURE 6 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 6. Male genitalia (top—lateral view, middle—plan view, bottom—aedeagus extracted, lateral view) A. M. granatus n. sp. Peru, Rodríguez de Mendoza, prep. genit. KF-2736 B. M. placida n. sp. Ecuador, Zamora, prep. genit. KW-20-021 C. M. benigni tessmanni, Peru, Alto Río Nieva, prep. genit. KF-H_241 D. M. benigni tessmanni, Ecuador, Río Troya, prep. genit. KF-6282
FIGURE 4 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 4. Adults (left—dorsum, right—venter) A. M. granatus n. sp. ♂ Holotype, Ecuador, Paquisha Alto B. M. granatus n. sp. ♂ Paratype, Peru, Alto Río Nieva C. M. granatus n. sp.♀, Ecuador, San Andrés D. M. placida n. sp. ♂ Holotype, Ecuador, Zamora - Arcoiris
FIGURE 2 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 2. Adults (left—dorsum, right—venter) A. M. prattorum udima n. ssp. ♂ Paratype, Peru, vía Hacienda Udima B. M. prattorum udima n. ssp. ♀ Paratype, Peru, vía Hacienda Udima C. M. inducta n. sp. ♂ Holotype, Peru, Lagunas Arrebiatadas D. M. inducta n. sp. ♀ Paratype, Ecuador, Jimbura —San Andrés road
FIGURE 1 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 1. Adults (left—dorsum, right—venter) A. M. ronda n. sp.♂ Holotype, Peru, Laguna Salahuindo B. M. ronda n. sp.♀ Paratype, Peru, Laguna Salahuindo C. M. ronda amplia n. ssp. ♂ Holotype, Peru, Kañaris D. M. rufanalis (?) ♂, Peru, Hacienda Udima
Dataset and scripts for "Multimode characterization of an optical beam deflection setup"
<p>The main files are the following :</p> <p><strong>Multimode_characterization_of_an_optical_beam_deflection_setup.pdf </strong>is the preprint of the article.</p> <p><strong>flexion_analysis.m</strong> is a Matlab script which analyses the amplitudes and frequencies of the contrasts corresponding to deflexion modes of the cantilever and stored in flexion_data.mat to compute the OBD spot position and size, and plot Figs. 3a, 3b, and 5b of the article.<br><strong>torsion_analysis.m</strong> is a Matlab script which analyses the amplitudes and frequencies of the contrasts corresponding to torsion modes of the cantilever and stored in flexion_data.mat to compute the OBD spot position and size, and plot Figs. 3c, 3d, and 5c of the article.<br><strong>ModeNumberStudy.m</strong> is a Matlab script which creates Fig. 4 of the article.</p> <p>All other matlab scripts and mat files are dependecies, their use is commented in the main scripts.</p> <p> </p>
'Reconciling Surface Deflections From Simulations of Global Mantle Convection' : Numerical model dataset
<p><strong>Output data from TERRA simulations included in 'Reconciling Surface Deflections From Simulations of Global Mantle Convection'</strong></p> <p>Dataset includes:</p> <ul> <li>Full density field (`NC_visc_dens_037.tar.gz`)</li> <li>Radial stresses (directory `radial_stresses`)</li> <li>Spherical harmonic coefficients for density field (`density_sph.037`)</li> <li>Radial viscosity factors (`visc.dat`)</li> </ul> <p>Radial stresses are calculated at depths of:</p> <ul> <li>0 km (surface)</li> <li>45 km</li> <li>180 km</li> <li>270 km</li> </ul> <p>and with various amounts of shallow structure removed:</p> <ul> <li>NC_DT_rmir0 - No shallow structure removed</li> <li>NC_DT_rmir1 - 45 km removed</li> <li>NC_DT_rmir2 - 90 km removed</li> <li>NC_DT_rmir3 - 135 km removed</li> <li>NC_DT_rmir5 - 225 km removed</li> <li>NC_DT_rmir7 - 270 km removed</li> </ul>
FWD, LWD, and Transverse Profile Measurements for Introduction of Cycle Path Deflection Bowl Parameters
<p>Collected data for the scientific article "Structural Stability of Cycle Paths - Introducing Cycle Path Deflection Bowl Parameters from FWD measurements". FWD, LWD, and Transverse profile measurement data. </p>
DEFLECT I: Keystone Heart Embolic Deflection Trial
ClinicalTrials.gov study NCT01448421. IPD Sharing: Not stated. Countries: 0. Publications: 1.
Data from: Eyespots deflect predator attack increasing fitness and promoting the evolution of phenotypic plasticity
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Data from: Defensive posture in a terrestrial salamander deflects predatory strikes irrespective of body size
A wide variety of prey use defensive postures as a means of protection from predators. Many salamanders engage in broadly similar defensive postures, which may function as a warning signal and reduce the probability of attack, or may deflect predator attacks away from vital body parts. The extent to which these strategies (i.e. aposematism and deflection) act exclusively or synergistically, however, remains unknown. We deployed clay salamanders in the field, manipulating size (small, large) and posture (resting, defensive), and documented attack rates across three predator types. Competing risks analysis revealed that attack rates were affected by model size, deployment period, and leaf litter depth at the site of deployment, whereas model posture had no significant effect. Model size and posture did not interact, indicating that defensive posture was ineffective in deterring attack irrespective of prey size. Model prey in the defensive posture received significantly more attacks on the tail irrespective of size, and the defensive posture was more effective at deflecting avian attacks compared to mammal predation. We conclude that defensive posture increases tail conspicuousness without increasing predation risk, and primarily functions to deflect attacks away from vital body parts. The efficacy of defection may be further increased by tail undulation, however our use of static models means that we cannot exclude aposematic or deimatic functions for such movements. Our results provide important support for the deflection hypothesis in explaining antipredator behavior, and thereby set the stage for additional research targeting the functionality of attack deflection in natural predator-prey encounters.
FIGURE 16 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 16. Huancabamba Deflection area map with new taxa known localities.
Asymmetrical Solar Wind Deflection in the Martian Magnetosheath
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The deflection of veel
<p>A dataset about the deflection of <em>veel </em>in Dutch, based on the C-CLAMP corpus.</p>
Data from: Moth tails divert bat attack: evolution of acoustic deflection
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Data from: Defensive posture in a terrestrial salamander deflects predatory strikes irrespective of body size
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Numerical Simulations of Laboratory-Scale, Hypervelocity-Impact Experiments for Asteroid-Deflection Code Validation
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Tail autotomy works as a pre-capture defense by deflecting attacks
<p>Caudal autotomy is a dramatic antipredator adaptation where prey shed their tail in order to escape capture by a predator. The mechanism underlying the effectiveness of caudal autotomy as a pre-capture defense has not been thoroughly investigated. We tested two non-exclusive hypotheses, that caudal autotomy works by providing the predator with a 'consolation prize' that makes it break off the hunt to consume the shed tail, and the deflection hypothesis, where the autotomy event directs predator attacks to the autotomized tail enabling prey escape. Our experiment utilized domestic dogs Canis familiaris as model predator engaged to chase a snake-like stimulus with a detachable tail. The tail was manipulated to vary in length (long vs. short) and conspicuousness (green vs. blue), with the prediction that dog attacks on the tail should increase with length under the consolation prize hypothesis, and conspicuous color under the deflection hypothesis. The tail was attacked on 35% of trials, supporting the potential for pre-capture autotomy to offer anti-predator benefits. Dogs were attracted to the tail when it was conspicuously colored, but not when it was longer. This supports the idea that deflection of predator attacks through visual effects is the prime antipredator mechanism underlying the effectiveness of caudal autotomy as opposed to provision of a consolation prize meal.</p>
NEUROvascular NAVigation With Remotely Controlled Deflectable Guidewire, Study II (NeuroNAV Study II)
ClinicalTrials.gov study NCT06972966. IPD Sharing: NO. Countries: 1. Publications: 0.
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