Active reconfiguration of cytoplasmic lipid droplets governs migration of nutrient-limited phytoplankton.

Nutrient availability, along with light and temperature, drives marine primary production. The ability to migrate vertically, a critical trait of motile phytoplankton, allows species to optimize nutrient uptake, storage, and growth. However, this traditional view discounts the possibility that migration in nutrient-limited waters may be actively modulated by the emergence of energy-storing organelles. Here, we report that bloom-forming raphidophytes harness energy-storing cytoplasmic lipid droplets (LDs) to biomechanically regulate vertical migration in nutrient-limited settings. LDs grow and translocate directionally within the cytoplasm, steering strain-specific shifts in the speed, trajectory, and stability of swimming cells. Nutrient reincorporation restores their swimming traits, mediated by an active reconfiguration of LD size and coordinates. A mathematical model of cell mechanics establishes the mechanistic coupling between intracellular changes and emergent migratory behavior. Amenable to the associated photophysiology, LD-governed behavioral shift highlights an exquisite microbial strategy toward niche expansion and resource optimization in nutrient-limited oceans.

The effect of the finite size of ions and Debye layer overspill on the screened Coulomb interactions between charged flat plates.

Screened repulsion between uniformly charged plates with an intervening electrolyte is analyzed for strongly overlapped electrical double layers (EDL), accounting for the steric effect of ions and their expulsion from EDL edges into the surrounding solution. As a generalization of a study by Philipse et al. which does not account for these effects, an analytical expression is derived for the repulsion pressure in the limit of infinitely long plates with a zero-field assumption, which agrees closely with the corresponding numerical solution at low inter-plate separations. Our results show an augmented repulsive pressure for finite-sized ions at strong EDL overlaps. For plates with a finite lateral size, we demonstrate a further extended domain of low inter-plate gaps where the repulsion pressure increases with ion size due to a strong interplay between the steric interaction of ions and the EDL overspill phenomenon, considered earlier in a study by Ghosal & Sherwood limited to the linear Debye-Hückel regime (which cannot account for the steric effect of ions). This investigation on a simple model should enhance our understanding of the interaction between charged particles in electrophoresis, nanoscale self-assembly, active particles, and various other electrokinetic systems.

Joule heating-induced particle manipulation on a microfluidic chip.

We develop an electrokinetic technique that continuously manipulates colloidal particles to concentrate into patterned particulate groups in an energy efficient way, by exclusive harnessing of the intrinsic Joule heating effects. Our technique exploits the alternating current electrothermal flow phenomenon which is generated due to the interaction between non-uniform electric and thermal fields. Highly non-uniform electric field generates sharp temperature gradients by generating spatially-varying Joule heat that varies along the radial direction from a concentrated point hotspot. Sharp temperature gradients induce a local variation in electric properties which, in turn, generate a strong electrothermal vortex. The imposed fluid flow brings the colloidal particles at the centre of the hotspot and enables particle aggregation. Furthermore, maneuvering structures of the Joule heating spots, different patterns of particle clustering may be formed in a low power budget, thus opening up a new realm of on-chip particle manipulation process without necessitating a highly focused laser beam which is much complicated and demands higher power budget. This technique can find its use in Lab-on-a-chip devices to manipulate particle groups, including biological cells.

Patterned surface charges coupled with thermal gradients may create giant augmentations of solute dispersion in electro-osmosis of viscoelastic fluids.

Augmenting the dispersion of a solute species and fluidic mixing remains a challenging proposition in electrically actuated microfluidic devices, primarily due to an inherent plug-like nature of the velocity profile under uniform surface charge conditions. While a judicious patterning of surface charges may obviate some of the concerning challenges, the consequent improvement in solute dispersion may turn out to be marginal. Here, we show that by exploiting a unique coupling of patterned surface charges with intrinsically induced thermal gradients, it may be possible to realize giant augmentations in solute dispersion in electro-osmotic flows. This is effectively mediated by the phenomena of Joule heating and surface heat dissipation, so as to induce local variations in electrical properties. Combined with the rheological premises of a viscoelastic fluid that are typically reminiscent of common biofluids handled in lab-on-a-chip-based micro-devices, our results demonstrate that the consequent electro-hydrodynamic forcing may open up favourable windows for augmented hydrodynamic dispersion, which has not yet been unveiled.

Electrically modulated capillary filling imbibition of nematic liquid crystals.

The flow of nematic liquid crystals (NLCs) in the presence of an electric field is typically characterized by the variation in its rheological properties due to transition in its molecular arrangements. Here, we bring out a nontrivial interplay of a consequent alteration in the resistive viscous effects and driving electrocapillary interactions, toward maneuvering the capillary filling dynamics over miniaturized scales. Considering a dynamic interplay of the relevant bulk and interfacial forces acting in tandem, our results converge nicely to previously reported experimental data. Finally, we attempt a scaling analysis to bring forth further insight to the reported observations. Our analysis paves the way for the development of microfluidic strategies with previously unexplored paradigms of interaction between electrical and fluidic phenomenon, providing with an augmented controllability on capillary filling as compared to tthose reported to be achievable by the existing strategies. This, in turn, holds utilitarian scopes in improved designs of functional capillarities in electro-optical systems, electrorheological utilities, electrokinetic flow control, as well as in interfacing and imaging systems for biomedical microdevices.

Electroosmosis of Viscoelastic Fluids: Role of Wall Depletion Layer.

We investigate electroosmotic flow of two immiscible viscoelastic fluids in a parallel plate microchannel. Contrary to traditional analysis, the effect of the depletion layer is incorporated near the walls, thereby capturing the complex coupling between rheology and electrokinetics. Toward ensuring realistic prediction, we show the dependence of electroosmotic flow rate on the solution pH and polymer concentration of the complex fluid. In order to assess our theoretical predictions, we have further performed experiments on electroosmosis of an aqueous solution of polyacrylamide (PAAm). Our analysis reveals that neglecting the existence of a depletion layer would result in grossly incorrect predictions of the electroosmotic transport of such fluids. These findings are likely to be of importance in understanding electroosmotically driven transport of complex fluids, including biological fluids, in confined microfluidic environments.

Electro-osmosis of nematic liquid crystals under weak anchoring and second-order surface effects.

Advent of nematic liquid crystal flows has attracted renewed attention in view of microfluidic transport phenomena. Among various transport processes, electro-osmosis stands as one of the efficient flow actuation mechanisms through narrow confinements. In the present study, we explore the electrically actuated flow of an ordered nematic fluid with ionic inclusions, taking into account the influences from surface-induced elasticity and electrical double layer (EDL) phenomena. Toward this, we devise the coupled flow governing equations from fundamental free-energy analysis, considering the contributions from first- and second-order elastic, dielectric, flexoelectric, charged surface polarization, ionic and entropic energies. The present study focuses on the influence of surface charge and elasticity effects in the resulting linear electro-osmosis through a slit-type microchannel whose surfaces are chemically treated to display a homeotropic-type weak anchoring state. An optical periodic stripe configuration of the nematic director has been observed, especially for higher electric fields, wherein the Ericksen number for the dynamic study is restricted to the order of unity. Contrary to the isotropic electrolytes, the EDL potential in this case was found to be dependent on the external field strength. Through a systematic investigation, we brought out the fact that the wavelength of the oscillating patterns is dictated mainly by the external field, while the amplitude depends on most of the physical variables ranging from the anchoring strength and the flexoelectric coefficients to the surface charge density and electrical double layer thickness.

Solvent-mediated nonelectrostatic ion-ion interactions predicting anomalies in electrophoresis.

We study the effects of solvent-mediated nonelectrostatic ion-ion interactions on electrophoretic mobility of a charged spherical particle. To this end, we consider the case of low surface electrostatic potential resulting in the linearization of the governing equations, which enables us to deduce a closed-form analytical solution to the electrophoretic mobility. We subsequently compare our results to the standard model using Henry's approach and report the changes brought about by the nonelectrostatic potential. The classical approach to determine the electrophoretic mobility underpredicts the particle velocity when compared with experiments. We show that this issue can be resolved by taking into account nonelectrostatic interactions. Our analysis further reveals the phenomenon of electrophoretic mobility reversal that has been experimentally observed in numerous previous studies.

Resolving Anomalies in Predicting Electrokinetic Energy Conversion Efficiencies of Nanofluidic Devices.

We devise a new approach for capturing complex interfacial interactions over reduced length scales, towards predicting electrokinetic energy conversion efficiencies of nanofluidic devices. By embedding several aspects of intermolecular interactions in continuum based formalism, we show that our simple theory becomes capable of representing complex interconnections between electro-mechanics and hydrodynamics over reduced length scales. The predictions from our model are supported by reported experimental data, and are in excellent quantitative agreement with molecular dynamics simulations. The present model, thus, may be employed to rationalize the discrepancies between low energy conversion efficiencies of nanofluidic channels that have been realized from experiments, and the impractically high energy conversion efficiencies that have been routinely predicted by the existing theories.

Electro-capillary effects in capillary filling dynamics of electrorheological fluids.

The flow of electrorheological fluids is characterized by an apparent increase in viscosity manifested by the yield stress property of the fluid, which is a function of the applied electric field and the concentration of the suspended solute phase within the dielectric medium. This property of electrorheological fluids generally hinders flow through a capillary if the imposed shear stress is lower than the induced yield stress. This results in a plug-like zone in the flow profile, thus giving the fluid Bingham plastic properties. In the present work, we study such influences of the yield stress on the capillary filling dynamics of an electrorheological fluid by employing a rheologically consistent reduced order formalism. One important feature of the theoretical formalism is its ability to address the intricate interplay between the surface tension and viscous forces, both of which depend sensitively on the electric field. Our analysis reveals that the progress of the capillary front is hindered at an intermediate temporal regime, which is attributable to the increase of the span of the plug-zone across the channel width with time. With a preliminary understanding on the cessation of the capillary front advancement due to the yield stress property of the electrorheological fluids, we further strive to achieve a basic comparison with an experimental study made earlier. Reasonable agreements with the reported data support our theoretical framework. Comprehensive scaling analysis brings further insight to our reported observations over various temporal regimes.

Alterations in streaming potential in presence of time periodic pressure-driven flow of a power law fluid in narrow confinements with nonelectrostatic ion-ion interactions.

We study the coupled effect of electrokinetic phenomena and fluid rheology in altering the induced streaming potential in narrow fluidic confinements, which is manifested by establishing a time periodic pressure-driven flow in presence of electrical double layer phenomenon. However, in sharp contrast with reported literature, we take into account nonelectrostatic ion-ion interactions toward estimating the same in addition to electrostatic interactions and steric effects. We employ power law based rheological model for estimating the induced streaming potential. We bring out an intricate interaction between nonelectrostatic interactions and fluid rheology on the concerned electrokinetic phenomena, bearing immense consequences toward designing of integrated lab-on-a-chip-based microdevices and nanodevices.

Electro-osmosis of electrorheological fluids.

Electrorheological fluids are suspensions that are characterized by a strong functional dependence of the constitutive behavior of the fluids on the electric field. In this work, we consider electro-osmosis of an electrorheological fluid through a channel where a transverse, nonuniform electric field is spontaneously induced due to the presence of an electric double layer that is manifested due to surface charge density at the channel wall. We reveal a nonlinear interplay between the applied electric field, the induced electric field, and the observed flow profiles, which is fundamentally distinctive from other types of nonlinear electrokinetic effects that have been extensively discussed in the literature, in a sense that here an interaction between the applied electric field, the induced electric field, and the dependence of the rheology on the resultant electric field happens to be the focal source of nonlinearity in the observed phenomena. We analyze the electro-osmotic flow control through the exploitation of a combined nonlinear interplay of the driving electrokinetic forces and the resistive viscous interactions, which gives rise to distinctive flow regimes as compared to those realized in cases of either Newtonian fluids or non-Newtonian fluids having electric-field-independent flow rheology.

Effects of solvent-mediated nonelectrostatic ion-ion interactions on a streaming potential in microchannels and nanochannels.

Here, we capture the consequences of solvent-mediated nonelectrostatic ion-ion interactions, coupled with the considerations of finite-sized effects of the ionic species, on electrokinetic transport in narrow fluidic confinements. We consider pressure-driven flow in microchannels and nanochannels in the presence of electrical double layer effects and analyze the establishment of a streaming potential as mediated by a Yukawa-like pair potential that integrates the ion specificity with the governing nonelectrostatic interactions. We bring out the influences of these interactions on electroviscous effects manifested due to the establishment of the streaming potential. Our considerations provide a plausible explanation for the gross overestimation of electrokinetic energy conversion efficiencies as predicted by classical electrical double layer theories that ignore nonelectrostatic interactions between the ionic species.