Slingshot spiders build tensed, underdamped webs for ultrafast launches and speedy halts.

We develop a mathematical model to capture the web dynamics of slingshot spiders (Araneae: Theridiosomatidae), which utilize a tension line to deform their orb webs into conical springs to hunt flying insects. Slingshot spiders are characterized by their ultrafast launch speeds and accelerations (exceeding 1300 [Formula: see text]), however a theoretical approach to characterize the underlying spatiotemporal web dynamics remains missing. To address this knowledge gap, we develop a 2D-coupled damped oscillator model of the web. Our model reveals three key insights into the dynamics of slingshot motion. First, the tension line plays a dual role: enabling the spider to load elastic energy into the web for a quick launch (in milliseconds) to displacements of 10-15 body lengths, but also enabling the spider to halt quickly, attenuating inertial oscillations. Second, the dominant energy dissipation mechanism is viscous drag by the silk lines - acting as a low Reynolds number parachute. Third, the web exhibits underdamped oscillatory dynamics through a finely-tuned balance between the radial line forces, the tension line force and viscous drag dissipation. Together, our work suggests that the conical geometry and tension-line enables the slingshot web to act as both an elastic spring and a shock absorber, for the multi-functional roles of risky predation and self-preservation.

Tunable hygromorphism: structural implications of low molecular weight gels and electrospun nanofibers in bilayer composites.

This investigation highlights the potential for electrospun nanofiber mats and self-assembled nanofiber networks to be interfaced synergistically to induce hygromorphic behaviour. Control poly(vinyl alcohol) (PVA) electrospun active layers and 1,3:2,4-di-p-methylbenyliedene sorbitol (MDBS) self-assembled passive layers encapsulated in an ethylene oxide-epichlorohydrin (EO-EPI) copolymer matrix were fabricated to examine the influence of composition on the properties guiding hygromorphism, such as water transport, layer thickness, and layer modulus. Experimentally determined material constants were utilized in conjunction with mathematical modeling to determine ideal layer properties. It was revealed that the active layer with the highest PVA content exhibited the fastest water transport, and the passive layer with the highest MDBS content displayed the slowest water transport. However, the hygromorphic bilayer fabricated utilizing the lowest PVA content and the highest MDBS fraction was predicted to induce the highest change in curvature due to the lower modulus and thickness of the PVA nanofiber active layer. Decreasing the MDBS content reduced the passive layer modulus while increasing water transport, which theoretically reduced the overall bilayer curvature. The hygromorphic bilayer composites fabricated using these ideal control layers exhibited folding bias and response variations dependent upon active layer composition and imposed folding directions. By utilizing the favorable force balances between the active layer with the lower PVA content and the passive layer with the highest MDBS amount in conjunction with folding bias in a non-preferential direction, it was possible to achieve hygromorphic unfolding and refolding with hydration. Through modelling and individual layer examination, a unique platform built on two independent fiber networks has been designed to achieve biomimetic hygromorphism in synthetic bilayer composites.

Poroelastic plant-inspired structures & materials to sense, regulate flow, and move.

Despite their lack of a nervous system and muscles, plants are able to feel, regulate flow, and move. Such abilities are achieved through complex multi-scale couplings between biology, chemistry, and physics, making them difficult to decipher. A promising approach is to decompose plant responses in different blocks that can be modeled independently, and combined later on for a more holistic view. In this perspective, we examine the most recent strategies for designing plant-inspired soft devices that leverage poroelastic principles to sense, manipulate flow, and even generate motion. We will start at the organism scale, and study how plants can use poroelasticity to carry informationin-lieuof a nervous system. Then, we will go down in size and look at how plants manage to passively regulate flow at the microscopic scale using valves with encoded geometric non-linearities. Lastly, we will see at an even smaller scale, at the nanoscopic scale, how fibers orientation in plants' tissues allow them to induce motion using water instead of muscles.

Ultrafast launch of slingshot spiders using conical silk webs.

In the Theridiosomatidae spider family, at least three genera (Epeirotypus, Naatlo and Theridiosoma) use their three-dimensional cone-shaped webs as ultrafast slingshots that catapult both the spider and the web towards prey [1-3]. Also known as slingshot spiders, theridiosomatids build three-dimensional conical webs with a tension line directly attached to the center of the web. In 1932, Hingston [1] hypothesized that the slingshot spider releases the tension line using its front legs, while holding the web with its rear legs. Coddington [2] detailed how female spiders meticulously build their webs line-by-line. But lacking to date has been quantification of spider kinematics, such as displacement, velocity and acceleration. Here we report the first quantification of theridiosomatid motion, revealing that slingshot spiders generate the fastest arachnid full body motion through use of their webs for external latch-mediated spring actuation [4].

Restricting Molecular Mobility in Polymer Nanocomposites with Self-Assembling Low-Molecular-Weight Gel Additives.

Multiscale investigation of molecular gel additives in polymer matrices guides understanding of how solution-state assemblies result in mechanically enhanced, solid-state nanocomposites. Model polymers, poly(ethylene oxide- co-epichlorohydrin) (EO-EPI) and poly(vinyl acetate) (PVAc), were utilized as matrices and reinforced by cholesterol-pyridine (CP) nanofiber networks. The CP nanofillers suppress ethylene oxide segment melting for EO-EPI composites, whereas for PVAc nanocomposites, cause a polymer-gel dissociation transition. Incorporation of crystalline CP fiber networks led to an order of magnitude increase in tensile storage modulus due to restrictions on polymer chain mobility. This decrease in molecular mobility was confirmed by decreased loss moduli for both EO-EPI and PVAc composites. Excitingly, PVAc nanocomposites display an additional relaxation mode caused by release of PVAc chains from the transient molecular gel assembly. For both EO-EPI and PVAc composites, bulk flow can be suppressed to temperatures up to 100 °C by simply increasing the CP concentration.