For nearly 450 million years, mycorrhizal fungi have constructed networks to collect and trade nutrient resources with plant roots1,2. Owing to their dependence on host-derived carbon, these fungi face conflicting trade-offs in building networks that balance construction costs against geographical coverage and long-distance resource transport to and from roots3. How they navigate these design challenges is unclear4. Here, to monitor the construction of living trade networks, we built a custom-designed robot for high-throughput time-lapse imaging that could track over 500,000 fungal nodes simultaneously. We then measured around 100,000 cytoplasmic flow trajectories inside the networks. We found that mycorrhizal fungi build networks as self-regulating travelling waves-pulses of growing tips pull an expanding wave of nutrient-absorbing mycelium, the density of which is self-regulated by fusion. This design offers a solution to conflicting trade demands because relatively small carbon investments fuel fungal range expansions beyond nutrient-depletion zones, fostering exploration for plant partners and nutrients. Over time, networks maintained highly constant transport efficiencies back to roots, while simultaneously adding loops that shorten paths to potential new trade partners. Fungi further enhance transport flux by both widening hyphal tubes and driving faster flows along 'trunk routes' of the network5. Our findings provide evidence that symbiotic fungi control network-level structure and flows to meet trade demands, and illuminate the design principles of a symbiotic supply-chain network shaped by millions of years of natural selection.
Soft amorphous materials are viscoelastic solids ubiquitously found around us, from clays and cementitious pastes to emulsions and physical gels encountered in food or biomedical engineering. Under an external deformation, these materials undergo a noteworthy transition from a solid to a liquid state that reshapes the material microstructure. This yielding transition was the main theme of a workshop held from January 9 to 13, 2023 at the Lorentz Center in Leiden. The manuscript presented here offers a critical perspective on the subject, synthesizing insights from the various brainstorming sessions and informal discussions that unfolded during this week of vibrant exchange of ideas. The result of these exchanges takes the form of a series of open questions that represent outstanding experimental, numerical, and theoretical challenges to be tackled in the near future.
Early in the COVID-19 pandemic, there were reports that the spread of the SARS-CoV-2 virus occurred via an airborne route created by asymptomatic individuals. This transport pathway inspired us to better understand air flows in everyday activities such as speech, which, surprisingly, had been little studied. We undertook this challenge using 1) laboratory experiments designed to visualize exhalations accompanying simple phrases and 2) numerical solutions of the Navier-Stokes equations for conditions representative of breathing and speaking; both research directions were new to all of the co-authors. The results suggested that in spite of the complexity of speech, the vortical nature of plosive sounds produce significant transport in front of a speaker, so much so that even after a few seconds of speech in a poorly ventilated space the mitigation recommended by the "six-foot rule" is questionable. In addition, the studies led us to investigate how such flows occur for professional musicians performing in opera, the effects of masks on the air flow, and the interplay between contact time and separation distance when thinking about strategies to minimize contact with an airborne virus. As a result of their expertise, the authors were involved in other pandemic-related projects and some of these educational and research connections are documented also, e.g., modeling of crowds and student projects such as developing a suite of CO2 sensors to monitor the effectiveness of ventilation. Finally, these activities occurred during a time of rapid evolution of institutional policies in response to the pandemic and we record the evolution of policies at Princeton University, including times of restricted access to the lab followed by the stepwise re-start of different laboratory and university activities.
Clusters of contaminations have been identified within rehearsing choirs during the COVID-19 pan-demic. In particular, singing and playing wind instruments are known to generate enhanced release of respiratory droplets, which are then transported by the expiratory flows. By tracking the air exhaled by professional opera singers and musicians from the MET Orchestra in New York City, we measure the spatial extent of the various air flows in opera. While loud singing is often associated with fast flows, professional opera singers and musicians are usually exhaling air flows slower than the air jets exhaled by a person breathing at rest. However, we identify a few situations leading to the release of rapid air jets that are able to enhance the transport of pathogenic droplets within an orchestra. Finally, we show how singing with a facemask and covering the bell of a wind instrument provide a strong reduction of the transport of respiratory droplets, in addition to the filtration features of a mask.
Shear thickening denotes the reversible increase in viscosity of a suspension of rigid particles under external shear. This ubiquitous phenomenon has been documented in a broad variety of multiphase particulate systems, while its microscopic origin has been successively attributed to hydrodynamic interactions and frictional contact between particles. The relative contribution of these two phenomena to the magnitude of shear thickening is still highly debated, and we report here a discriminating experimental study using a model shear-thickening suspension that allows us to independently tune both the surface chemistry and the surface roughness of the particles. We show here that both properties matter when it comes to continuous shear thickening (CST) and that the presence of hydrogen bonds between the particles is essential to achieve discontinuous shear thickening (DST) by enhancing solid friction between closely contacting particles. Moreover, a simple argument allows us to predict the onset of CST, which for these very rough particles occurs at a critical volume fraction much lower than that previously reported in the literature. Finally, we demonstrate how mixtures of particles with opposing surface chemistry make it possible to finely tune the shear-thickening response of the suspension at a fixed volume fraction, paving the way for a fine control of the shear-thickening transition in engineering applications.
Helmet continuous positive applied pressure is a form of noninvasive ventilation (NIV) that has been used to provide respiratory support to COVID-19 patients. Helmet NIV is low-cost, readily available, provides viral filters between the patient and clinician, and may reduce the need for invasive ventilation. Its widespread adoption has been limited, however, by the lack of a respiratory monitoring system needed to address known safety vulnerabilities and to monitor patients. To address these safety and clinical needs, we developed an inexpensive respiratory monitoring system based on readily available components suitable for local manufacture. Open-source design and manufacturing documents are provided. The monitoring system comprises flow, pressure, and CO2 sensors on the expiratory path of the helmet circuit and a central remote station to monitor up to 20 patients. The system is validated in bench tests, in human-subject tests on healthy volunteers, and in experiments that compare respiratory features obtained at the expiratory path to simultaneous ground-truth measurements from proximal sensors. Measurements of flow and pressure at the expiratory path are shown to deviate at high flow rates, and the tidal volumes reported via the expiratory path are systematically underestimated. Helmet monitoring systems exhibit high-flow rate, nonlinear effects from flow and helmet dynamics. These deviations are found to be within a reasonable margin and should, in principle, allow for calibration, correction, and deployment of clinically accurate derived quantities.
Carbonated droplets deposited on a superhydrophobic surface float on a self-generated cushion of gas.
Face masks are used widely to mitigate the spread of infectious diseases. While their main purpose is to filter pathogenic droplets, masks also represent a porous barrier to exhaled and inhaled air flow. In this study, we characterize the aerodynamic effect of the presence of a mask by tracking the air exhaled by a person through a mask, using both infrared imaging and particle image velocimetry performed on illuminated fog droplets surrounding a subject. We show how a mask confines the exhaled flows within tens of centimeters in front of a person breathing or speaking. In addition, we show that the tissue of common surgical face masks has a low permeability, which efficiently transforms the jetlike flows of exhalation produced during breathing or speaking into quasivertical buoyancy-driven flows. Therefore, wearing a mask offers a strong mitigation of direct transport of infectious material in addition to providing a filtering function. By comparing results on human subjects and model experiments, we propose a model to rationalize how a mask changes the air flow, and thus we provide quantitative insights that are useful for descriptions of disease transmission.
A drop of an aqueous suspension of nanoparticles placed on a substrate forms a solid deposit as it dries. For dilute suspensions, particles accumulate within a narrow ring at the drop edge, whereas a uniform coating covering the entire wetted area forms for concentrated suspensions. In between these extremes, we report two additional regimes characterized by non-uniform deposit thicknesses and by distinct crack morphologies. We show that both the deposit shape and the number of cracks are controlled exclusively by the initial particle volume fraction. The different regimes share a common avalanche-like crack propagation dynamics, as a result of the delamination of the deposit from the substrate.
This paper is associated with a video winner of a 2020 American Physical Society'sDivision of Fluid Dynamics (DFD) Milton van Dyke Award for work presented at theDFD Gallery of Fluid Motion. The original video is available online at the Gallery of FluidMotion,https://doi.org/10.1103/APS.DFD.2020.GFM.V0067
As first described by Leidenfrost, liquid droplets levitate over their own vapor when placed on a sufficiently hot substrate. The Leidenfrost effect not only confers remarkable properties such as mechanical and thermal insulation, zero adhesion, and extreme mobility but also requires a high energetic thermal cost. We describe here a previously unexplored approach using active liquids able to sustain levitation in the absence of any external forcing at ambient temperature. We focus on the particular case of carbonated water placed on a superhydrophobic solid and demonstrate how millimetric fizzy drops self-generate a gas cushion that provides levitation on time scales on the order of a minute. Last, we generalize this new regime to different kinds of chemically reactive droplets able to jump from the Cassie-Baxter state to a levitating regime, paving the way to the levitation of nonvolatile liquids.
Asphaltenes, heavy aromatic components of crude oil, are known to adsorb on surfaces and can lead to pipe clogging or hinder oil recovery. Because of their multicomponent structure, the details of their interactions with surfaces are complex. We investigate the effect of the physicochemical properties of the substrate on the extent and mechanism of this adsorption. Using wetting measurements, we relate the initial kinetics of deposition to the interfacial energy of the surface. We then quantify the longterm adsorption dynamics using a quartz crystal microbalance and ellipsometry. Finally, we investigate the mechanism and morphology of adsorption with force spectroscopy measurements as a function of surface chemistry. We determine different adsorption regimes differing in orientation, packing density, and initial kinetics on different substrate functionalizations. Specifically, we find that alkane substrates delay the initial monolayer formation, fluorinated surfaces exhibit fast adsorption but low bonding strength, and hydroxyl substrates lead to a different adsorption orientation and a high packing density of the asphaltene layer.
Asphaltenes are heavy aromatic components of crude oil. Their complex chemical makeup-an aromatic core surrounded by aliphatic side chains-enables them to adhere to most surfaces. Their buildup in pipes can result in clogging and lead to interruption of production operations and expensive mechanical cleaning. We demonstrate the use of liquid-impregnated surfaces (LIS) to prevent asphaltene deposition and buildup on substrates. Indeed, these surfaces expose a liquid interface to the working fluid, which combines the benefits of a dynamic defect-free surface and tunable interfacial properties. In contrast to bulk additives that are typically mixed into the oil phase, the impregnating liquid also provides the great benefit of protecting the underlying solid surface with a stable and minimal layer of lubricant, thereby reducing costs and eliminating the need for subsequent downstream removal. We first select and confirm the thermodynamic stability of a suitable lubricant and its lack of interaction with asphaltenes. By using a carefully selected system composed of a textured and functionalized solid substrate in conjunction with a fluorinated lubricant, we show that asphaltene adsorption is prevented over long time scales. We further demonstrate the possibility of building such a system with representative industrial materials such as aluminum and expose the resulting substrate to an external shear flow to simulate pipe flow conditions.
This paper is associated with a video winner of a 2019 American Physical Society's Division of Fluid Dynamics (DFD) Milton van Dyke Award for work presented at the DFD Gallery of Fluid Motion. The original video is available online at the Gallery of Fluid Motion, littps://doi.org/10.1103/APS.DFD.2019.GFM.V0082.
Shear thickening denotes the rapid and reversible increase in viscosity of a suspension of rigid particles under external shear. This ubiquitous phenomenon has been documented in a broad variety of multiphase particulate systems, while its microscopic origin has been successively attributed to hydrodynamic interactions and frictional contact between particles. The relative contribution of these two phenomena to the magnitude of shear thickening is still highly debated and we report here a discriminating experimental study using a model shear-thickening suspension that allows us to tune independently both the surface chemistry and the surface roughness of the particles. We show here that both properties matter when it comes to continuous shear thickening (CST) and that the presence of hydrogen bonds between the particles is essential to achieve discontinuous shear thickening (DST) by enhancing solid friction between closely contacting particles. Moreover, a simple argument allows us to predict the onset of CST, which for these highly-textured particles occurs at a critical volume fraction much lower than that previously reported in the literature. Finally, we demonstrate how mixtures of particles with opposing surface chemistry make it possible to finely tune the shear-thickening response of the suspension at a fixed volume fraction, paving the way for a fine control of shear-thickening transition in engineering applications.