537 research outputs found

    The effect of advance ratio on the aerodynamics of revolving wings

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    Recent studies have demonstrated that a quasi-steady model closely matches the instantaneous force produced by an insect wing during hovering flight. It is not clear, however, if such methods extend to forward flight. In this study we use a dynamically scaled robotic model of the fruit fly Drosophila melanogaster to investigate the forces produced by a wing revolving at constant angular velocity while simultaneously translating at velocities appropriate for forward flight. Because the forward and angular velocities were constant wing inertia was negligible, and the measured forces can be attributed to fluid dynamic phenomena. The combined forward and revolving motions of the wing produce a time-dependent free-stream velocity profile, which suggests that added mass forces make a contribution to the measured forces. We find that the forces due added mass make a small, but measurable, component of the total force and are in excellent agreement with theoretical values. Lift and drag coefficients are calculated from the force traces after subtracting the contributions due to added mass. The lift and drag coefficients, for fixed angle of attack, are not constant for non-zero advance ratios, but rather vary in magnitude throughout the stroke. This observation implies that modifications of the quasi-steady model are required in order to predict accurately the instantaneous forces produced during forward flight. We show that the dependence of the lift and drag coefficients upon advance ratio and stroke position can be characterized effectively in terms of the tip velocity ratio – the ratio of the chordwise components of flow velocity at the wing tip due to translation and revolution. On this basis we develop a modified quasi-steady model that can account for the varying magnitudes of the lift and drag coefficients. Our model may also resolve discrepancies in past measurements of wing performance based on translational and revolving motion

    A linear systems analysis of the yaw dynamics of a dynamically scaled insect model

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    Recent studies suggest that fruit flies use subtle changes to their wing motion to actively generate forces during aerial maneuvers. In addition, it has been estimated that the passive rotational damping caused by the flapping wings of an insect is around two orders of magnitude greater than that for the body alone. At present, however, the relationships between the active regulation of wing kinematics, passive damping produced by the flapping wings and the overall trajectory of the animal are still poorly understood. In this study, we use a dynamically scaled robotic model equipped with a torque feedback mechanism to study the dynamics of yaw turns in the fruit fly Drosophila melanogaster. Four plausible mechanisms for the active generation of yaw torque are examined. The mechanisms deform the wing kinematics of hovering in order to introduce asymmetry that results in the active production of yaw torque by the flapping wings. The results demonstrate that the stroke-averaged yaw torque is well approximated by a model that is linear with respect to both the yaw velocity and the magnitude of the kinematic deformations. Dynamic measurements, in which the yaw torque produced by the flapping wings was used in real-time to determine the rotation of the robot, suggest that a first-order linear model with stroke-average coefficients accurately captures the yaw dynamics of the system. Finally, an analysis of the stroke-average dynamics suggests that both damping and inertia will be important factors during rapid body saccades of a fruit fly

    Branched 1-Manifolds and Presentations of Solenoids

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    The aim of the project was to study the presentations of solenoids by branched 1-manifolds. We begin by studying two properties of branched 1-manifolds which effect the presentation of solenoids, orientability and recurrence. Solenoids are shown to come in two varieties, those presented by orientable branched 1-manifolds and those presented by nonorientable branched 1-manifolds. Two methods of determining whether or not a branched 1-manifold is orientable are given. Recurrence is shown to be a necessary and sufficient condition for a branched 1-manifold to present a solenoid. We then show how the question of whether or not a branched 1-manifold is recurrent can be converted into question in graph theory for which there exist efficient algorithms. Next we consider two special types of presentations, elementary presentations and (p, fj)-block presentations, which allow us to extract algebraic invariants for the equivalence of solenoids. A slightly stronger version of a result of Williams [39] is obtained which states that any solenoid with a fixed point is equivalent to one presented by an elementary presentation. The proof is constructive and gives a method for finding elementary presentation given a presentation of a solenoid with a fixed point. Williams has shown, [39], that there is a complete invariant for the equivalence of solenoids given by an elementary presentation in terms of the shift equivalence of endomorphisms of a free group. We prove a result which shows that every solenoid can be given by a countably infinite number of equivalent (p, q)-block presentations. The (p, q)-block presentations again allow us to find invariants for the equivalence of solenoids in terms of the shift equivalence of endomorphisms of a free group. Finally we consider further invariants for the equivalence of solenoids which are derived from the endomorphism invariants. First we examine the invariants which arise upon abelianizing the free group in question. Second we introduce new invariants which reflect some of the non-abelian character of these endomorphisms. These new non-abelian invariants are then used to solve a problem posed by Williams in [39]

    Integrative Model of Drosophila Flight

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    This paper presents a framework for simulating the flight dynamics and control strategies of the fruit fly Drosophila melanogaster. The framework consists of five main components: an articulated rigid-body simulation, a model of the aerodynamic forces and moments, a sensory systems model, a control model, and an environment model. In the rigid-body simulation the fly is represented by a system of three rigid bodies connected by a pair of actuated ball joints. At each instant of the simulation, the aerodynamic forces and moments acting on the wings and body of the fly are calculated using an empirically derived quasi-steady model. The pattern of wing kinematics is based on data captured from high-speed video sequences. The forces and moments produced by the wings are modulated by deforming the base wing kinematics along certain characteristic actuation modes. Models of the fly’s visual and mechanosensory systems are used to generate inputs to a controller that sets the magnitude of each actuation mode, thus modulating the forces produced by the wings. This simulation framework provides a quantitative test bed for examining the possible control strategies employed by flying insects. Examples demonstrating pitch rate, velocity, altitude, and flight speed control, as well as visually guided centering in a corridor are presented

    Neuromuscular control of wingbeat kinematics in Anna's hummingbirds (Calypte anna)

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    Hummingbirds can maintain the highest wingbeat frequencies of any flying vertebrate – a feat accomplished by the large pectoral muscles that power the wing strokes. An unusual feature of these muscles is that they are activated by one or a few spikes per cycle as revealed by electromyogram recordings (EMGs). The relatively simple nature of this activation pattern provides an opportunity to understand how motor units are recruited to modulate limb kinematics. Hummingbirds made to fly in low-density air responded by moderately increasing wingbeat frequency and substantially increasing the wing stroke amplitude as compared with flight in normal air. There was little change in the number of spikes per EMG burst in the pectoralis major muscle between flight in normal and low-density heliox (mean=1.4 spikes cycle^(–1)). However the spike amplitude, which we take to be an indication of the number of active motor units, increased in concert with the wing stroke amplitude, 1.7 times the value in air. We also challenged the hummingbirds using transient load lifting to elicit maximum burst performance. During maximum load lifting, both wing stroke amplitude and wingbeat frequency increased substantially above those values during hovering flight. The number of spikes per EMG burst increased to a mean of 3.3 per cycle, and the maximum spike amplitude increased to approximately 1.6 times those values during flight in heliox. These results suggest that hummingbirds recruit additional motor units (spatial recruitment) to regulate wing stroke amplitude but that temporal recruitment is also required to maintain maximum stroke amplitude at the highest wingbeat frequencies

    A New Low Reynolds Number Facility for Active Flow Control Applications

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    Recent interest in gaining understanding of the dynamics and behavior of the leading-edge vortex structure observed in biological flight systems has prompted the construction of a new low Reynolds number facility. This facility, a recirculating oil tunnel, gives several distinct advantages over similar facilities, utilizing water or air as the working fluid, for this kind of study. Additionally, as understanding is gained, active flow control strategies leading to the stabilization of the leading-edge vortex structure will be investigated, and this facility is specially equipped to enable this study. The tunnel has been designed and installed at the California Institute of Technology Graduate Aeronautical Laboratories. Design features of the facility will be discussed, along with some preliminary measurements conducted on a NACA 0012 wing

    Unsteadiness in Flow over a Flat Plate at Angle-of-Attack at Low Reynolds Numbers

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    Flow over an impulsively started low-aspect-ratio flat plate at angle-of-attack is investigated for a Reynolds number of 300. Numerical simulations, validated by a companion experiment, are performed to study the influence of aspect ratio, angle of attack, and planform geometry on the interaction of the leading-edge and tip vortices and resulting lift and drag coefficients. Aspect ratio is found to significantly influence the wake pattern and the force experienced by the plate. For large aspect ratio plates, leading-edge vortices evolved into hairpin vortices that eventually detached from the plate, interacting with the tip vortices in a complex manner. Separation of the leading-edge vortex is delayed to some extent by having convective transport of the spanwise vorticity as observed in flow over elliptic, semicircular, and delta-shaped planforms. The time at which lift achieves its maximum is observed to be fairly constant over different aspect ratios, angles of attack, and planform geometries during the initial transient. Preliminary results are also presented for flow over plates with steady actuation near the leading edge

    Force production and flow structure of the leading edge vortex on flapping wings at high and low Reynolds numbers

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    The elevated aerodynamic performance of insects has been attributed in part to the generation and maintenance of a stable region of vorticity known as the leading edge vortex (LEV). One explanation for the stability of the LEV is that spiraling axial flow within the vortex core drains energy into the tip vortex, forming a leading-edge spiral vortex analogous to the flow structure generated by delta wing aircraft. However, whereas spiral flow is a conspicuous feature of flapping wings at Reynolds numbers (Re) of 5000, similar experiments at Re=100 failed to identify a comparable structure. We used a dynamically scaled robot to investigate both the forces and the flows created by a wing undergoing identical motion at Re of ~120 and ~1400. In both cases, motion at constant angular velocity and fixed angle of attack generated a stable LEV with no evidence of shedding. At Re=1400, flow visualization indicated an intense narrow region of spanwise flow within the core of the LEV, a feature conspicuously absent at Re=120. The results suggest that the transport of vorticity from the leading edge to the wake that permits prolonged vortex attachment takes different forms at different Re

    Progress in Interferometry for LISA at JPL

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    Recent advances at JPL in experimentation and design for LISA interferometry include the demonstration of Time Delay Interferometry using electronically separated end stations, a new arm-locking design with improved gain and stability, and progress in flight readiness of digital and analog electronics for phase measurements.Comment: 11 pages, 9 figures, LISA 8 Symposium, Stanford University, 201

    Cortical tau is associated with microstructural imaging biomarkers of neurite density and dendritic complexity in Alzheimer's disease

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    INTRODUCTION: In Alzheimer's disease (AD), hyperphosphorylated tau is closely associated with focal neurodegeneration, but the mechanism remains uncertain. METHODS: We quantified cortical microstructure using neurite orientation dispersion and density imaging in 14 individuals with young onset AD. Diffusion tensor imaging measured mean diffusivity (MD). Amyloid beta and tau positron emission tomography were acquired and associations with microstructural measures were assessed. RESULTS: When regional volume was adjusted for, in the medial temporal lobe there was a significant negative association between neurite density and tau (partial R2  = 0.56, p = 0.008) and between orientation dispersion and tau (partial R2  = 0.66, p = 0.002), but not between MD and tau. In a wider cortical composite, there was an association between orientation dispersion and tau (partial R2  = 0.43, p = 0.030), but not between other measures and tau. DISCUSSION: Our findings are consistent with tau causing first dendritic pruning (reducing dispersion/complexity) followed by neuronal loss. Advanced magnetic resonance imaging (MRI) microstructural measures have the potential to provide information relating to underlying tau deposition
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