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Two-dimensional rheological laminar hemodynamics through a diseased tapered artery with a mild stenosis present is simulated theoretically and computationally. The effect of different metallic nanoparticles homogeneously suspended in the blood is considered, motivated by drug delivery (pharmacology) applications. The Eringen micropolar model has been deployed for hemorheological characteristics in the whole arterial region. The conservation equations for mass, linear momentum, angular momentum (micro-rotation), and energy and nanoparticle species are normalized by employing suitable non-dimensional variables. The transformed equations are solved numerically subject to physically appropriate boundary conditions using the finite element method with the variational formulation scheme available in the FreeFEM++ code. A good correlation is achieved between the FreeFEM++ computations and existing results. The effect of selected parameters (taper angle, Prandtl number, Womersley parameter, pulsatile constants, and volumetric concentration) on velocity, temperature, and microrotational (Eringen angular) velocity has been calculated for a stenosed arterial segment. Wall shear stress, volumetric flow rate, and hemodynamic impedance of blood flow are also computed. Colour contours and graphs are employed to visualize the simulated blood flow characteristics. It is observed that by increasing Prandtl number (Pr), the micro-rotational velocity decreases i.e., microelement (blood cell) spin is suppressed. Wall shear stress decreases with the increment in pulsatile parameters (B and e), whereas linear velocity increases with a decrement in these parameters. Furthermore, the velocity decreases in the tapered region with elevation in the Womersley parameter (α). The simulations are relevant to transport phenomena in pharmacology and nano-drug targeted delivery in hematology.

Social cues, such as eye gaze and pointing fingers, can increase the prioritisation of specific locations for cognitive processing. A previous study using a manual reaching task showed that, although both gaze and pointing cues altered target prioritisation (reaction times [RTs]), only pointing cues affected action execution (trajectory deviations). These differential effects of gaze and pointing cues on action execution could be because the gaze cue was conveyed through a disembodied head; hence, the model lacked the potential for a body part (i.e., hands) to interact with the target. In the present study, the image of a male gaze model, whose gaze direction coincided with two potential target locations, was centrally presented. The model either had his arms and hands extended underneath the potential target locations, indicating the potential to act on the targets (Experiment 1), or had his arms crossed in front of his chest, indicating the absence of potential to act (Experiment 2). Participants reached to a target that followed a nonpredictive gaze cue at one of three stimulus onset asynchronies. RTs and reach trajectories of the movements to cued and uncued targets were analysed. RTs showed a facilitation effect for both experiments, whereas trajectory analysis revealed facilitatory and inhibitory effects, but only in Experiment 1 when the model could potentially act on the targets. The results of this study suggested that when the gaze model had the potential to interact with the cued target location, the model's gaze affected not only target prioritisation but also movement execution.

The present study considers two-dimensional mathematical modeling of non-Newtonian nanofluid hemodynamics with heat and mass transfer in a stenosed coronary artery in the presence of a radial magnetic field. The second-grade differential viscoelastic constitutive model is adopted for blood to mimic non-Newtonian characteristics, and blood is considered to contain a homogenous suspension of nanoparticles. The Vogel model is employed to simulate the variation of blood viscosity as a function of temperature.The governing equations are an extension of the Navier-Stokes equations with linear Boussinesq's approximation and Buongiorno's nanoscale model (which simulates both heat and mass transfer). The conservation equations are normalized by employing appropriate nondimensional variables. It is assumed that the maximum height of the stenosis is small in comparison with the radius of the artery, and, furthermore, that the radius of the artery and length of the stenotic region are of comparable magnitude. To study the influence of vessel geometry on blood flow and nanoparticle transport, variation in the design and size of the stenosis is considered in the domain. The transformed equations are solved numerically by means of the finite element method based on the variational approach and simulated using the FreeFEM++ code. A detailed grid-independence study is included. Blood flow, heat, and mass transfer characteristics are examined for the effects of selected geometric, nanoscale, rheological, viscosity, and magnetic parameters, that is, stenotic diameter (d), viscoelastic parameter (λ 1 ), thermophoresis parameter (N t ), Brownian motion parameter (N b ), and magnetic body force parameter (M) at the throat of the stenosis and throughout the arterial domain. The velocity, temperature, and nanoparticle concentration fields are also visualized through instantaneous patterns of contours. An increase in magnetic and thermophoresis parameters is found to enhance the temperature, nanoparticle concentration, and skin-friction coefficient. Increasing Brownian motion parameter is observed to accelerate the blood flow. Narrower stenosis significantly alters the temperature and nanoparticle distributions and magnitudes. The novelty of the study relates to the combination of geometric complexity, multiphysical nanoscale, and thermomagnetic behavior, and also the simultaneous presence of biorheological behavior (all of which arise in actual cardiovascular heat transfer phenomena) in a single work with extensive visualization of the flow, heat, and mass transfer characteristics. The simulations are relevant to the diffusion of nano-drugs in magnettargeted treatment of stenosed arterial disease. K E Y W O R D Sarterial stenosis, finite element method, magnetohydrodynamics, nano-drugs, non-Newtonian blood flow, thermophoresis, Vogel's model