ライフサイエンスコーパス: hydrodynamic

1 order is often frustrated by the presence of hydrodynamics.

2 self-formed lobes that scale with backwater hydrodynamics.

3 tal momenta, a manifestation of relativistic hydrodynamics.

4 io calculations that predict wavelike phonon hydrodynamics.

5 a phase diagram for air evolution regarding hydrodynamics.

6 he feedback mechanisms between reactions and hydrodynamics.

7 ations in CSF production, absorption, or its hydrodynamics.

8 upon suitable balance between magnetism and hydrodynamics.

9 onal motion predicted by classical colloidal hydrodynamics.

10 the process that gives rise to turbulence in hydrodynamics(1)-represents the mechanism by which a sma

11 Nevertheless, life history and hydrodynamics also covary with latitude-these also affec

12 New hydrodynamic analyses demonstrate that Palaeozoic jawles

13 We couple spatially-explicit 2-D hydrodynamic analyses with economic models, and find tha

14 enhance flagellar thrust; however, detailed hydrodynamic analysis supporting this claim is lacking.

15 ctrum to a level suitable for a quantitative hydrodynamic analysis.

16 We report here kinetic, thermodynamic, hydrodynamic and computational studies that show that a

17 rpretation of our results by determining the hydrodynamic and solvation properties of our OmpW-micell

18 Pa/9min) on molecular mass distribution, and hydrodynamic and structural parameters of amylose (maize

19 The combination of two-dimensional radiation hydrodynamic and three-dimensional hybrid simulations sh

20 ndation for fundamental studies of bacterial hydrodynamics and also provides a novel, to our knowledg

21 gy and astrophysics to biology, magneto- and hydrodynamics and condensed matter physics.

22 s in present use and based on incompressible hydrodynamics and interaction with a rigid ocean floor o

23 xplained by considering the coupling between hydrodynamics and muscle contraction characteristics, as

24 been made in the understanding of microbial hydrodynamics and surface interactions over the last dec

25 chment location and rate depend on the local hydrodynamics and, as revealed by a mathematical model b

26 gmented aqueductal cerebrospinal fluid (CSF) hydrodynamics, and expansion of summated brain and CSF v

27 confluence of muscle contractile properties, hydrodynamics, and the high speeds required likely impos

28 By focusing on hydrodynamic aspects of the problem, we apply group theo

29 d, optimizing fouling mitigation strategies, hydrodynamics at the membrane surface, and membrane modu

30 opy ( D( )/ D( ) ~ 7.6), consistent with the hydrodynamic behavior predicted for such a long, nearly

31 le of discrete water molecules in modulating hydrodynamic behaviors of individual ions is poorly unde

32 e position to a near-neighbour, could obtain hydrodynamic benefits if they exhibit a tailbeat phase d

33 mework for synthesizing DO observations with hydrodynamic-biogeochemical model simulations and meteor

34 and fast-flowing water adapted species with hydrodynamic bodies are significantly associated with se

35 Our work reveals that hydrodynamics can profoundly affect how bacteria compete

36 Results indicate that the use of hydrodynamic cavitation amplifies the detection capabili

37 y combining enzymatic digestion of the meat, hydrodynamic cavitation to disassemble pathogens from th

38 Our use of hydrodynamic cavitation to separate pathogens is compare

39 Our analysis further reveals that hydrodynamic cell reorientation and Lagrangian flow stru

40 The hydrodynamic communication channel therefore plays a lar

41 earch indicate that an appropriate choice of hydrodynamic conditions can minimize bacteria accumulati

42 However, the effects of hydrodynamic conditions on spatiotemporal deposition pat

43 ting parameters, such as feed concentration, hydrodynamic conditions, and feed temperature, on the so

44 tuations in their sources and changes in the hydrodynamic conditions, respectively.

45 mporal deposition patterns between different hydrodynamic conditions: high and low permeate water flu

46 tant solvent motion that effectively induces hydrodynamic correlations between particles.

47 using several dynamical models and find that hydrodynamic correlations, depending on their range, can

48 onsistent with predictions from contemporary hydrodynamic cosmological simulations that were not tune

49 ibution of surface excitations, and suppress hydrodynamic counterflow.

50 this shear-induced structuring is driven by hydrodynamic coupling between the flocs and the confinin

51 Hydrodynamic coupling effects pertinent to quartz crysta

52 Intracranial volumetry and aqueductal CSF hydrodynamics (CSF peak-to-peak velocity amplitude and a

53 Here, we establish a hydrodynamic description of aggregating granular gases t

54 ch electrical transport features a universal hydrodynamic description, even at room temperature(1,2).

55 noparticles (citrate-coated) with an initial hydrodynamic diameter (D(h)) of 24.6 +/- 0.4 nm examined

56 The NLCs were evaluated for hydrodynamic diameter (Z-ave), polydispersity index (PDI

57 mall gold nanoparticles (core diameter 2 nm; hydrodynamic diameter 3-4 nm) across the BBB was studied

58 le and stable in aqueous-based media, with a hydrodynamic diameter of 229 +/- 28 nm.

59 synthesized by in situ polymerization, has a hydrodynamic diameter of 25 nm and can be customized via

60 weight percent (wt%) content of IO on GO and hydrodynamic diameter of 414 nm, which is associated wit

61 The nanosensors show hydrodynamic diameter ranging from 234.2 +/- 3.5 to 801.

62 ld in the SWIR (14-33%), compact size (13 nm hydrodynamic diameter), and long-term stability in aqueo

63 loids were found to increase with decreasing hydrodynamic diameter, D(h), and were proportional to 1/

64 d particle size distribution and the average hydrodynamic diameter.

65 correlation spectroscopy detected that their hydrodynamic diameters ranged from 207 to 222 nm.

66 elf-diffusion coefficients D determining the hydrodynamic dimensions.

67 The methodology relies on hydrodynamic dispersion modeling of a smooth analyte gra

68 prey school, even if this results in higher hydrodynamic drag.

69 The crucial hydrodynamic driver in this situation is the depression

70 d a detailed calculation based on a nonlocal hydrodynamic Drude model for the metal permittivity.

71 We find a host of spectacular optical and hydrodynamic effects driven by ultralow applied field (E

72 model accounting for multibond kinetics and hydrodynamic effects due to the flow of a cellular suspe

73 esent a comprehensive investigation into the hydrodynamic effects of mastigonemes using a genetically

74 d exchange of water drives locomotion due to hydrodynamic effects.

75 morphology is compatible with a diversity of hydrodynamic efficiencies including passive control of w

76 lly more prolate headshields exhibit maximum hydrodynamic efficiency when swimming free from substrat

77 Investigations using cyclic voltammetry and hydrodynamic electrochemistry show that the presence of

78 t finite carrier density are consistent with hydrodynamic electron flow in graphene(5-8), a clear dem

79 (2-11), the fundamental spatial structure of hydrodynamic electrons-the Poiseuille flow profile-has r

80 ary minimum are relatively more resistant to hydrodynamic energies (including detachment associated e

81 lects other bottom current features, such as hydrodynamic energy, grain size, nutrient transport, etc

82 in soil C(org) but, when combined with high hydrodynamic energy, significant erosion occurred.

83 jellyfish's muscle system and its bell in a hydrodynamic environment, we explore the swimming elicit

84 Eu-type generalized hydrodynamic equations have been derived from the Boltzm

85 Galerkin method to solve Eu-type generalized hydrodynamic equations in multidimensions.

86 in models that account for the geography and hydrodynamic features of the region support the hypothes

87 virtual parcels of water are tracked through hydrodynamic fields, provides an increasingly popular fr

88 rtex street, similar to that of the inverted hydrodynamic fish trail.

89 explain the interaction between whiskers and hydrodynamic fish trails.

90 This method involves local sampling using hydrodynamic flow confinement of a lysis buffer, followe

91 Here, we probe the hydrodynamic flow field around a catalytically active co

92 ies of fermion transport, with relevance for hydrodynamic flow of electrons, neutrons, and quarks.

93 at low velocities, friction is controlled by hydrodynamic flow through the porous hydrogel network an

94 l quantity for distinguishing ballistic from hydrodynamic flow.

95 on of bacteria to insoluble substrates under hydrodynamic flow.

96 rnal factors such as ions, (macro)molecules, hydrodynamic flows, or electromagnetic fields can be dir

97 dyes were used in order to characterize the hydrodynamic focusing as a function of flow rate ratio o

98 ed using a single cell flow system, in which hydrodynamic focusing drives cells along in a single fil

99 The hydrodynamic force experienced by a CTC was also studied

100 ambers of the microfluidic device, where the hydrodynamic force then induces precise rotation of the

101 e-dependent capillary adhesion attributed to hydrodynamic forces above a critical separation rate.

102 We find that the torque required by the hydrodynamic forces and body inertia exhibits a wave pat

103 , an active cell cortex and nucleus, and for hydrodynamic forces and flow of the extracellular fluid,

104 atics, we present direct measurements of the hydrodynamic forces generated by flagella with and witho

105 ell, especially by counteracting part of the hydrodynamic forces of the bloodstream encountered by th

106 We find that the hydrodynamic forces required for this entrainment strong

107 In vitro hydrodynamic forces such as compression, shear and tensi

108 which circumvents these limitations by using hydrodynamic forces to exert nanoscale-precision control

109 he presence of blood flow and the associated hydrodynamic forces, reducing the likelihood of adhesion

110 perse particulates that experience transient hydrodynamic forces.

111 bled high temporal and spatial resolution of hydrodynamic forces.

112 ly variable diazotrophic community driven by hydrodynamic forcing in an upwelling system.

113 otrophic community and its relationship with hydrodynamic forcing.

114 e use a recently extended "Smoothed Particle Hydrodynamics" formulation to examine potential mechanis

115 collar filter, thanks to the formation of a 'hydrodynamic gasket' above the collar.

116 puzzling observation of a difference in spin hydrodynamic generation for particles and anti-particles

117 have been significant interests in the spin hydrodynamic generation phenomenon from multiple discipl

118 microfluidic crystal lattices, we show that hydrodynamic gradients hinder transverse bacterial dispe

119 Although various aspects of electron hydrodynamics have been revealed in recent experiments(2

120 on rising oil droplets and their associated hydrodynamic impacts including flow fields and momentum

121 differences in morphology, growth rates, and hydrodynamic impacts.

122 PC-MRI is widely used to evaluate CSF hydrodynamics in normal pressure hydrocephalus (NPH), Ch

123 strates the anomalous landscape for electron hydrodynamics in systems beyond graphene, and presents e

124 ization, within the framework of generalized hydrodynamics, including diffusive corrections.

125 This demonstrates that hydrodynamics influence species interaction and evolutio

126 ivity in a mouse model of hemophilia A after hydrodynamic injection of Cas9-sgAlb and B domain-delete

127 ion in animals that were later challenged by hydrodynamic injection or transduction with adeno-associ

128 mice were transfected with an HBV plasmid by hydrodynamic injection.

129 re was enriched in liver tumors initiated by hydrodynamic injections of activated-NOTCH as compared w

130 method is compatible with electrokinetic and hydrodynamic injections, with detection limits of 70 and

131 We suggest that hydrodynamic instabilities adjust the angular-momentum d

132 Chemical, morphological, mechanical and hydrodynamic instabilities at the metal anode produce un

133 pair with other partners as a result of the hydrodynamic instabilities generated by collective cell

134 ming planets within the disk(2) or (magneto-)hydrodynamic instabilities(3).

135 environments, e.g., induced by chemistry or hydrodynamic instabilities.

136 d solid-like resistance to morphological and hydrodynamic instability.

137 opulsion direction changes the nature of the hydrodynamic interaction from attractive to repulsive an

138 rises from the interplay between contact and hydrodynamic interaction, which channel seemingly errati

139 iour resulting only from the balance between hydrodynamic interactions and external alignment.

140 distributions while accounting for colloidal hydrodynamic interactions and thermodynamic non-ideality

141 These hydrodynamic interactions are shape dependent and can be

142 pen the way to a thorough description of the hydrodynamic interactions between such active particles

143 Our theory describes the elasto-capillary-hydrodynamic interactions between the membrane of the ba

144 develop a theoretical framework to model the hydrodynamic interactions between the tracer and the act

145 tion technique in order to include naturally hydrodynamic interactions in implicit solvent simulation

146 Hydrodynamic interactions play a role in synchronized mo

147 in the formulation to take into account the hydrodynamic interactions.

148 se flood hazard data from a ~90 m resolution hydrodynamic inundation model to demonstrate the impact

149 ion is co-determined by the spatial decay of hydrodynamic lift and the global deficiency of cell disp

150 t] dominates over [Formula: see text] in the hydrodynamic limit.

151 cell, time-resolved mechanical response to a hydrodynamic load.

152 ed plasticity, and particulate flow aided by hydrodynamic lubrication.

153 (0)-P with biophysical approaches, including hydrodynamic measurements and small-angle X-ray scatteri

154 Centering is achieved via a hydrodynamic mechanism based on Darcy friction between t

155 action of the cell projections, suggesting a hydrodynamic mechanism.

156 ng steady-state kinetic analysis as in other hydrodynamic methods.

157 We use hydrodynamic mobility to evaluate the size of spermidine

158 rodynamic separation utilizes differences in hydrodynamic mobility to separate bound DNA-biomolecule

159 ehavior, Lars Onsager proposed a statistical hydrodynamic model based on quantized vortices.

160 We used a hydrodynamic model, satellite images of resuspension eve

161 ian particle tracking framework and the BNAM hydrodynamic model, we found enhanced connectivity over

162 th the predictions from our elasto-capillary-hydrodynamic model.

163 nts are qualitatively described by a minimal hydrodynamic model.

164 Here we conduct climatology-hydrodynamic modeling to quantify the effects of sea lev

165 Using hydrodynamic modeling, we demonstrate that a mode where

166 Their locomotion imparts hydrodynamic momentum to the surrounding water in the fo

167 Spain (42.5 degrees N, 8.9 degrees W); (2) a hydrodynamic numerical model at 300 m spatial resolution

168 We quantified the kinematics and hydrodynamics of a diverse group of small swimming anima

169 mental setup that simulates the intracranial hydrodynamics of a pneumocephalus patient during flight.

170 ne bending elasticity, a property related to hydrodynamics of cells and organelles.

171 We confirm predictions based on hydrodynamics of fluid membranes, finding long-range cor

172 rical shape on the settling of sediments and hydrodynamics of turbidity currents in a narrow channel.

173 assical nucleation theory to the large-scale hydrodynamics on the droplet scale, bringing together tw

174 easily integrated with upstream electronic, hydrodynamic, or other focusing units to produce efficie

175 A plausible hydrodynamic origin of anomalous transport in simple por

176 The elasto-hydrodynamic origin of the fragmentation explains the st

177 lumns can be well predicted through coupling hydrodynamic parameters and surface complexation constan

178 ltracentrifugation was utilized to determine hydrodynamic parameters of reversibly associating specie

179 We report masses and hydrodynamic particle sizes of insoluble particles forme

180 Hydrodynamic performance varies with morphology, proximi

181 never been specifically investigated from a hydrodynamic perspective.

182 lipid systems at the mesoscopic scale where hydrodynamics plays an essential role, e.g. by modulatin

183 idic system only with the knowledge of local hydrodynamics, polymorphs, and comprehensive image analy

184 From this measurement, using a hydrodynamic power balance, we infer the mean flagellar

185 Increased hydrodynamic pressure in retracting cell projections nor

186 s, crucial for a better understanding of the hydrodynamic processes during such events and offering a

187 rgy and matter is driven by hydrological and hydrodynamic processes such as river and groundwater dis

188 The method, HAP-NMR (hydrodynamic profiling by NMR), is an extension of the p

189 deposited film in terms of viscoelastic and hydrodynamic properties are fulfilled.

190 models accurately predicted the experimental hydrodynamic properties measured for each structure.

191 can affect the chemically induced changes in hydrodynamic properties of fractures.

192 The critical role of two-phase hydrodynamic properties on non-Fickian transport and sat

193 e of OAS1 monomer and dimer, comparing their hydrodynamic properties with OAS2.

194 pumping systems are needed, neither for the hydrodynamic pumping of the mobile phase as in high-perf

195 Hydrodynamic radii measured in urine, cerebrospinal flui

196 er levels of phenolic proton intensities and hydrodynamic radii relative to the control starch-phenol

197 es information on diffusion coefficients and hydrodynamic radii.

198 the formation of aggregates with an average hydrodynamic radius 38 +/- 2 nm.

199 ts concentration, absolute molecular weight, hydrodynamic radius and intrinsic viscosity.

200 ligand surface density, which determine the hydrodynamic radius and optical absorption of such nanop

201 glycosidic linkages were analyzed by GC-MS, hydrodynamic radius and proton magnetic resonance of gel

202 Our focus is on determining the apparent hydrodynamic radius and the related accuracy bias, which

203 see text], diffuses as a particle of 600-nm hydrodynamic radius dissolved in water.

204 al diffusion remain valid, but the effective hydrodynamic radius grows linearly with protein volume f

205 was proven to allow the determination of the hydrodynamic radius of metal-containing nanoparticles, e

206 fer a high dynamic range to characterize the hydrodynamic radius of particles.

207 ated calcium phosphate solutions, PNS with a hydrodynamic radius of R(h) ~ 1 nm is formed and (ii) fo

208 The hydrodynamic radius of RNP particles (86 nm) precludes s

209 nd therefore is suited well to measuring the hydrodynamic radius of small molecules, proteins, supram

210 sample, the dissociation constant (K(d)) and hydrodynamic radius of the complex were determined to be

211 l to the optical-extinction-weighted average hydrodynamic radius of the particle systems.

212 to exist as alpha helices in solution with a hydrodynamic radius of ~3 nm in size.

213 rsion is capable of measuring accurately the hydrodynamic radius over several orders of magnitude.

214 ich is defined as the smallest change in the hydrodynamic radius that Taylor dispersion can resolve a

215 rtition coefficients of solutes differing in hydrodynamic radius were consistent with size-based theo

216 e more sensitive to protein structure (i.e., hydrodynamic radius), than to molecular mass (size).

217 re, and aqueductal cerebrospinal fluid (CSF) hydrodynamics relative to spaceflight and to establish a

218 A hydrodynamic representation of the numerical simulations

219 atio of propulsive force/swimming speed (the hydrodynamic resistance) and the power output of the fla

220 of the boundary fluid to reduce near-surface hydrodynamic resistance, thus promoting particle-surface

221 It combines picomolar sensitivity with high hydrodynamic resolution, and can be carried out with pho

222 ects at low shock pressures and leading to a hydrodynamic response at the highest loading conditions.

223 Our analysis of the nonlocal hydrodynamic response leads to the conjecture that the d

224 ively described by a model that accounts for hydrodynamic screening of packed cilia and the chemomech

225 Here, we present Hydro-Seq, a scalable hydrodynamic scRNA-seq barcoding technique, for high-thr

226 Single molecule free solution hydrodynamic separation utilizes differences in hydrodyn

227 es in AnMBRs and emphasize the importance of hydrodynamic shear and membrane surface properties on th

228 ive DLVO force between particle pairs to the hydrodynamic shear force opposing it.

229 We reported that hydrodynamic shear stress (SS) mechanoregulates inflamma

230 To measure the sensitivity to hydrodynamic signals in these receiver cells, we present

231 ation and coordination among schoolmates via hydrodynamic signals within the pulsed jet created by th

232 We demonstrate a radiation hydrodynamic simulation of optical vortex pulse-ablated

233 A two-dimensional (2-D) radiation hydrodynamic simulation reproduced the cone structure we

234 While a hydrodynamic simulation, analytical results, and dilutio

235 Here we report a radiation hydrodynamics simulation of early galaxy formation(11,12

236 Hydrodynamic simulations attribute this to the high Mach

237 Hydrodynamic simulations indicate that the highest-mass

238 Using hydrodynamic simulations of a RBC and parasite, where bo

239 that, by including this Magellanic Corona in hydrodynamic simulations of the Magellanic Clouds fallin

240 Using a theoretical model based on hydrodynamic singularities, we capture quantitatively th

241 quantification and the ability to measure in hydrodynamic situations, such as the bloodstream.

242 technique fractionates ENPs on the basis of hydrodynamic size and demonstrates a unique capability t

243 -linking with multiple GNPs), via a combined hydrodynamic size and electron microscopy analysis.

244 Reduction of hydrodynamic size and intrinsic viscosity was observed i

245 ree of substitution, contents of metal ions, hydrodynamic size distribution, intrinsic viscosity, pas

246 ptomagnetic readouts of signal phase lag and hydrodynamic size increase of MNPs, NECA-based target qu

247 MM hydrodynamic size increased with increasing l-alpha-phos

248 FA chain length impacted MM with hydrodynamic size increasing from 3.8 nm for decanoic ac

249 eter as measured by electron microscopy, and hydrodynamic size of the PFH nanodroplets were 150 to 23

250 The dual (charge and hydrodynamic size) separation mode was deemed necessary

251 trast-enhancing nanoparticles with different hydrodynamic sizes and relaxivity properties were compar

252 ile no relevant changes were observed in the hydrodynamic sizes of HTR-free compared to HTR-loaded na

253 present) conditions through a combination of hydrodynamic slip and surface interactions with asperiti

254 This surprising effect is due to hydrodynamic slip at the liquid-solid interface and occu

255 These cumulative findings reveal that hydrodynamic slip moderately decreases colloid bulk deli

256 Hydrodynamic slip was calibrated to experimentally obser

257 We prove that smoothed particle hydrodynamic (SPH) kernels can be used as edge features

258 e particle dynamics (DPD), smoothed particle hydrodynamics (SPH) and computational thermodynamics (CT

259 Here, we use the Smoothed Particle Hydrodynamics (SPH) approach to study various positional

260 t a microfluidic platform, the Time-Resolved Hydrodynamic Stretcher (TR-HS), which allows the investi

261 s these swimmers to exploit readily produced hydrodynamic structures.

262 These findings, in tandem with complementary hydrodynamic studies of CshA_RD1-17, indicate that this

263 bulence(11)-an instability known to occur in hydrodynamics, superconductors and Bose-Einstein condens

264 amics of an elastically pinned membrane in a hydrodynamic surrounding and subject to external forces.

265 rences, whereas the efficient and low-volume hydrodynamic system helps to lower the detection limit t

266 d the growth of HCC tumors induced using the hydrodynamic tail vein injection and orthotopic implanta

267 on was also observed in mouse CCA induced by hydrodynamic tail vein injection of notch intracellular

268 le immunocompetent mice with HCC, induced by hydrodynamic tail vein injection of proto-oncogenes, enh

269 Mice were given hydrodynamic tail vein injections of clustered regularly

270 e show in a mouse model of tyrosinaemia that hydrodynamic tail-vein injection of plasmid DNA encoding

271 ficient mice at the time of liver injury via hydrodynamic tail-vein injection.

272 By performing hydrodynamic tail-vein injections, we tested the impact

273 Active hydrodynamic theories are a powerful tool to study the e

274 ssipative) hard-sphere model and formulate a hydrodynamic theory based on Navier-Stokes equations to

275 present a kinetic approach complemented by a hydrodynamic theory for agents with mixed alignment symm

276 Hence, a modified diffusion model based on hydrodynamic theory is proposed to separate the direct (

277 the motor concentration, in agreement with a hydrodynamic theory.

278 hat the rear-squeezing mechanism is aided by hydrodynamics through a pressure gradient.

279 chronal swimmers may provide clues about the hydrodynamic traits shared by swimming and flying animal

280 Hydrodynamic transfer of the EAT gene to mice prevents h

281 on of two immiscible fluids and (ii) role of hydrodynamic transport and mixing between the low salini

282 mulations of coupled dynamic two-phase flow, hydrodynamic transport and wettability alteration in a 2

283 Our results will enable the study of hydrodynamic transport in quantum critical fluids releva

284 per trapping site, on the basis of a passive hydrodynamic trapping principle.

285 e, vertical tracking microscope, based on a 'hydrodynamic treadmill' with no bounds for motion along

286 Although there is a regional hydrodynamic trend across the uPBC, this variation is li

287 lyse and quantitatively model the ultra-fast hydrodynamic trigger waves in a universal framework of a

288 Here we present the discovery of 'hydrodynamic trigger waves' in cellular communities of t

289 ordinate their behaviour using variations of hydrodynamic trigger waves.

290 ytic efficacy was probed by using cyclic and hydrodynamic voltammetry on heterogeneous catalyst inks

291 ample, cyclic homopolymers exhibit a reduced hydrodynamic volume and a slower degradation profile com

292 tilized to separate mAb species with similar hydrodynamic volume but different surface characteristic

293 XRD spectra and hydrodynamic volume distribution revealed that growth of

294 ligosaccharides according to their charge to hydrodynamic volume ratios.

295 tography to obtain fractions sorted by size (hydrodynamic volume).

296 In hydrodynamics, vortex generation upon the transition fro

297 e behavior, structural dynamics and swimming hydrodynamics, we perform extensive computational simula

298 d mechanical modeling revealed that swimming hydrodynamics were accurately captured without including

299 Hydrodynamics, which generally describes the flow of a f

300 mbranes as the support, so that it optimizes hydrodynamics while maintaining even fluxes.