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      The ultrafast snap of a finger is mediated by skin friction

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          Abstract

          The snap of a finger has been used as a form of communication and music for millennia across human cultures. However, a systematic analysis of the dynamics of this rapid motion has not yet been performed. Using high-speed imaging and force sensors, we analyse the dynamics of the finger snap. We discover that the finger snap achieves peak angular accelerations of 1.6 × 10 6 ° s −2 in 7 ms, making it one of the fastest recorded angular accelerations the human body produces (exceeding professional baseball pitches). Our analysis reveals the central role of skin friction in mediating the snap dynamics by acting as a latch to control the resulting high velocities and accelerations. We evaluate the role of this frictional latch experimentally, by covering the thumb and middle finger with different materials to produce different friction coefficients and varying compressibility. In doing so, we reveal that the compressible, frictional latch of the finger pads likely operates in a regime optimally tuned for both friction and compression. We also develop a soft, compressible friction-based latch-mediated spring actuated model to further elucidate the key role of friction and how it interacts with a compressible latch. Our mathematical model reveals that friction plays a dual role in the finger snap, both aiding in force loading and energy storage while hindering energy release. Our work reveals how friction between surfaces can be harnessed as a tunable latch system and provides design insight towards the frictional complexity in many robotic and ultra-fast energy-release structures.

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          Most cited references42

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          Flexible mechanisms: the diverse roles of biological springs in vertebrate movement.

          The muscles that power vertebrate locomotion are associated with springy tissues, both within muscle and in connective tissue elements such as tendons. These springs share in common the same simple action: they stretch and store elastic strain energy when force is applied to them and recoil to release energy when force decays. Although this elastic action is simple, it serves a diverse set of functions, including metabolic energy conservation, amplification of muscle power output, attenuation of muscle power input, and rapid mechanical feedback that may aid in stability. In recent years, our understanding of the mechanisms and importance of biological springs in locomotion has advanced significantly, and it has been demonstrated that elastic mechanisms are essential for the effective function of the muscle motors that power movement. Here, we review some recent advances in our understanding of elastic mechanisms, with an emphasis on two proposed organizing principles. First, we review the evidence that the various functions of biological springs allow the locomotor system to operate beyond the bounds of intrinsic muscle properties, including metabolic and mechanical characteristics, as well as motor control processes. Second, we propose that an energy-based framework is useful for interpreting the diverse functions of series-elastic springs. In this framework, the direction and timing of the flow of energy between the body, the elastic element and the contracting muscle determine the function served by the elastic mechanism (e.g. energy conservation vs power amplification). We also review recent work demonstrating that structures such as tendons remodel more actively and behave more dynamically than previously assumed.
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            Biomechanics: deadly strike mechanism of a mantis shrimp.

            Stomatopods (mantis shrimp) are well known for the feeding appendages they use to smash shells and impale fish. Here we show that the peacock mantis shrimp (Odontodactylus scyllarus) generates an extremely fast strike that requires major energy storage and release, which we explain in terms of a saddle-shaped exoskeletal spring mechanism. High-speed images reveal the formation and collapse of vapour bubbles next to the prey due to swift movement of the appendage towards it, indicating that O. scyllarus may use destructive cavitation forces to damage its prey.
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              Elastic energy storage in the shoulder and the evolution of high-speed throwing in Homo

              Although some primates, including chimpanzees, throw objects occasionally 1,2 , only humans regularly throw projectiles with high speed and great accuracy. Darwin noted that humans’ unique throwing abilities, made possible when bipedalism emancipated the arms, enabled foragers to effectively hunt using projectiles 3 . However, there has been little consideration of the evolution of throwing in the years since Darwin made his observations, in part because of a lack of evidence on when, how, and why hominins evolved the ability to generate high-speed throws 4-8 . Here, we show using experimental studies of throwers that human throwing capabilities largely result from several derived anatomical features that enable elastic energy storage and release at the shoulder. These features first appear together approximately two million years ago in the species Homo erectus. Given archaeological evidence that suggests hunting activity intensified around this time 9 , we conclude that selection for throwing in order to hunt likely played an important role in the evolution of the human genus.
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                Author and article information

                Contributors
                Journal
                Journal of The Royal Society Interface
                J. R. Soc. Interface.
                The Royal Society
                1742-5662
                November 2021
                November 17 2021
                November 2021
                : 18
                : 184
                Affiliations
                [1 ]Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA 30311, USA
                [2 ]George W. Woodruff School of Mechanical Engineering, Georgia Tech, Atlanta, GA 30311, USA
                [3 ]Department of Physics, Harvey Mudd College, Claremont, CA 91711, USA
                Article
                10.1098/rsif.2021.0672
                34784775
                78da8cce-d3ff-4f88-85b1-9b63a6c9edab
                © 2021

                https://royalsociety.org/journals/ethics-policies/data-sharing-mining/

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