SummaryHow mechanical and biological processes are coordinated across cells, tissues, and organs to produce complex traits is a key question in biology. Cardamine hirsuta, a relative of Arabidopsis thaliana, uses an explosive mechanism to disperse its seeds. We show that this trait evolved through morphomechanical innovations at different spatial scales. At the organ scale, tension within the fruit wall generates the elastic energy required for explosion. This tension is produced by differential contraction of fruit wall tissues through an active mechanism involving turgor pressure, cell geometry, and wall properties of the epidermis. Explosive release of this tension is controlled at the cellular scale by asymmetric lignin deposition within endocarp b cells—a striking pattern that is strictly associated with explosive pod shatter across the Brassicaceae plant family. By bridging these different scales, we present an integrated mechanism for explosive seed dispersal that links evolutionary novelty with complex trait innovation.Video Abstract

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The coupling between community composition and climate change spans a gradient from no lags to strong lags. The no-lag hypothesis is the foundation of many ecophysiological models, correlative species distribution modelling and climate reconstruction approaches. Simple lag hypotheses have become prominent in disequilibrium ecology, proposing that communities track climate change following a fixed function or with a time delay. However, more complex dynamics are possible and may lead to memory effects and alternate unstable states. We develop graphical and analytic methods for assessing these scenarios and show that these dynamics can appear in even simple models. The overall implications are that (1) complex community dynamics may be common and (2) detailed knowledge of past climate change and community states will often be necessary yet sometimes insufficient to make predictions of a community's future state.

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We consider the dynamic snapping instability of elastic beams and shells. Using the Kirchhoff rod and Föppl-von Kármán plate equations, we study the stability, deformation modes, and snap-through dynamics of an elastic arch with clamped boundaries and subject to a concentrated load. For parameters typical of everyday and technological applications of snapping, we show that the stretchability of the arch plays a critical role in determining not only the postbuckling mode of deformation but also the timescale of snapping and the frequency of the arch's vibrations about its final equilibrium state. We show that the growth rate of the snap-through instability and its subsequent ringing frequency can both be interpreted physically as the result of a sound wave in the material propagating over a distance comparable to the length of the arch. Finally, we extend our analysis of the ringing frequency of indented arches to understand the 'pop' heard when everted shell structures snap-through to their stable state. Remarkably, we find that not only are the scaling laws for the ringing frequencies in these two scenarios identical but also the respective prefactors are numerically close; this allows us to develop a master curve for the frequency of ringing in snapping beams and shells. ULC 0.5 N load cell. p-2

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Convergent evolution is a phenomenon whereby similar traits evolved independently in not closely related species, and is often interpreted in functional terms. Spines in mollusk seashells are classically interpreted as having repeatedly evolved as a defense in response to shell-crushing predators. Here we consider the morphogenetic process that shapes these structures and underlies their repeated emergence. We develop a mathematical model for spine morphogenesis based on the mechanical interaction between the secreting mantle edge and the calcified shell edge to which the mantle adheres during shell growth. It is demonstrated that a large diversity of spine structures can be accounted for through small variations in control parameters of this natural mechanical process. This physical mechanism suggests that convergent evolution of spines can be understood through a generic morphogenetic process, and provides unique perspectives in understanding the phenotypic evolution of this second largest phylum in the animal kingdom.H omoplasy, the appearance of similar traits in separate evolutionary lineages as a result of convergence, parallelism, or evolutionary reversals, is a major concern in phylogenetic analysis for which it is viewed as noise. However, over the past two decades, homoplasy has also become a subject of increasing interest, stimulated by the rise of evolutionary developmental biology (evo devo) and the wish to uncover the developmental basis of this phenomenon (1-3). Spines constitute the most prominent ornamentation of mollusk shells and have evolved in many distantly related fossil and current mollusk species (at least 55 genera and 21 families of current gastropods; 10 genera and 8 families of current bivalves; 11 genera and 8 families of ammonoids; and 6 fossil nautiloid genera; see Fig. 1 for examples). Convergent evolution of spines in mollusks has been addressed in functional terms, these structures being interpreted as having evolved as a defense in response to shell-crushing predators (4-6). This hypothesis is itself the basis of the widely cited "escalation hypothesis," according to which long-term trends in the fossil record were caused by the evolutionary response of prey to predation pressure (7). The idea that convergent evolution of similar mollusk ornamentations might be fully explained in functional terms is based on the premise that similar characters, perceived as well designed for a presumed function, cannot conceivably have independently evolved fortuitously. Therefore, natural selection is thought to have repeatedly shaped similar functional traits out of random variations.Over the past two decades, there has been an increasing awareness that selectionist hypotheses on their own have partial explanatory value for understanding the evolution of biological form, because they do not address the origin of traits thought to increase reproductive success (8-10). In other words, even if spines act in some species as protection against predators, to hypothesize that this feature has sprea...

We demonstrate the passive control of viscous flow in a channel by using an elastic arch embedded in the flow. Depending on the fluid flux, the arch may 'snap' between two states -constricting and unconstricting -that differ in hydraulic conductivity by up to an order of magnitude. We use a combination of experiments at a macroscopic scale and theory to study the constricting and unconstricting states, and determine the critical flux required to transition between them. We show that such a device may be precisely tuned for use in a range of applications, and in particular has potential as a passive microfluidic fuse to prevent excessive fluxes in rigid-walled channels.