In nutrient-poor soils, carnivorous plants like the cape sundew supplement their diets by eating insects. To entice their prey, the cape sundew secretes droplets of sugary water. But unwary insects who land to feed soon find themselves unable to pull away from this viscoelastic liquid. Complex molecules in the fluid grant it elasticity, so when insects pull against it, the liquid stretches and pulls back instead of breaking up. Other carnivorous plants, like the pitcher plant, use similar non-Newtonian tricks to trap insects. (Video and image credit: Deep Look)
Many plants gain the soil-bound nutrients they need by trading with symbiotic fungi. Underground, these fungi spread networks that gather and store phosphorus, which they then trade with host plants to get the carbon they need. Research shows that the fungi can be shrewd traders, moving phosphorus from nutrient-rich areas to poorer ones in order to maximize their trade gains.
What you see above are snapshots of some of this transport within the fungal network. Notice how flow within the branching network changes direction. The fungus can force these flow reversals in a matter of seconds, allowing it to move nutrients to wherever the best returns are found. (Image and research credit: M. Whiteside et al.)
When brooding their eggs, penguins can rarely leave the nest, but answering nature’s call is still necessary. To keep the nest clean, Adélie penguins project their feces up to more than a meter away. A new study refines previous calculations on this subject and finds that the penguin’s rectum develops far higher pressures than that of humans.
In one hypothetical calculation, the authors estimate that a human of average height, capable of developing penguin-like rectal pressures, would project excrement more than 3 meters. In the authors’ words, “He/she should not use usual rest rooms.”
Knowing the likely range of contact for penguins is important primarily for zookeepers, who understandably would like to avoid such projectiles. (Image credit: H. Neufeld; research credit: H. Tajima and F. Fujisawa; via phys.org)
Flying snakes undulate through the air as they glide. But, unlike on land, these wiggles aren’t for propulsion. A new study shows instead that they are key to the snake staying stable in flight.
Upon take-off, a flying snake flattens its body, forming a wing-like shape that helps them generate lift and control drag. But while they glide, they also slither and pitch their tail.
Researchers recorded more than 150 flights by live snakes, then used that data to construct their own digital snake. The model could fly like a real snake or be tested without undulations to see what would happen. The researchers discovered that, without that mid-air slithering, the snake quickly lost control and rolled to the side. (Image and research credit: I. Yeaton et al.; via NYTimes; submitted by Kam-Yung Soh)
Some single-celled organisms, like dinoflagellates, light up when disturbed. This bioluminescence is considered a defense mechanism, triggered by threats to the organism. Now researchers are quantifying just what it takes to light up a single dinoflagellate.
Dinoflagellates respond both to stress caused by the fluid flow around them and to mechanical deformation — in other words, getting poked. Both methods involve bending and stretching the dinoflagellate’s cell wall, which stretches calcium-ion channels connected to bioluminescence. The researchers found that the intensity of the light produced depended both on the amount and speed of cell wall deformation.
The model built from their observations should help scientists better understand what forces cause a specific response. That means dinoflagellates could be used as a non-invasive means of understanding fluid flow around swimmers like dolphins or sea lions! (Image and research credit: M. Jalaal et al.; via APS Physics)
For juvenile fish, feeding is a challenge. Their small size — often less than 5 mm in length — makes hydrodynamically capturing prey much harder because of viscosity’s relatively larger effect on them. But size may not be the only factor in determining their success, as a new study shows.
Researchers studied feeding behaviors of two, equally-sized species’ larvae: zebrafish and guppies. The biggest difference between these two species is their developmental time prior to beginning to hunt on their own. Guppies develop five times longer than zebrafish larvae before they start feeding.
Both fish have the same hydrodynamic limitations to overcome. If you look closely at the first image, you’ll see fluid being pushed ahead of the fish as it swims. The researchers refer to this as a bow wave, and it effectively announces to any prey that the fish is approaching. To sneak up on prey, the fish has to be able to generate enough suction force to pull its food in from beyond the bow wave’s reach. The experiments showed that guppies were able to do this reliably, while zebrafish could not. The subsequent difference in their feeding success was stark: the guppies’ success rate was almost five times that of the zebrafish! (Image and research credit: T. Dial and G. Lauder, source; via G. Lauder)
Vibrate a pool of water, and you’ll get Faraday waves, ripple-like excitations that form their own distinctive pattern compared to the driving vibration. But you don’t have to vibrate a pure liquid to see Faraday waves. A recent study observed them in vibrated earthworms!
Odd as this may sound, the results make sense. When anesthetized (as they were in the experiments), earthworms are essentially a liquid wrapped in an elastic membrane, which is not so different from a droplet held together by surface tension.
But why vibrate earthworms in the first place? It turns out earthworms are a good model organism for studies of vertebrate neural systems, so observing how vibrations propagate through them can provide insight into how our own nervous systems transmit information. (Image, research, and submission credit: I. Maksymov and A. Pototsky)
Getting wet can be a problem for many animals. A wet insect could quickly become too heavy to fly, and a wet bird can struggle to stay warm. But these animals have a secret weapon: tiny, multi-scale roughness on their wings, scales, and feathers that helps them shed water. Watch the latest FYFD video to learn how! (Image and video credit: N. Sharp; research credit: S. Kim et al.)
Many plants have evolved an ability to move remarkably quickly. Often, this capability is driven by water. Here we see the moss Sphagnumaffine, which disperses its spores explosively. The process is triggered by the spore capsule gradually drying out; its shape changes from round to cylindrical, pressurizing the capsule. Once the internal pressure is high enough to overcome the strength of the capsule’s upper membrane, the capsule bursts, sending a plume of spores aloft. The sudden release of spore-laden air forms a vortex ring, which lifts the spores higher far more efficiently than they would be otherwise. (Image credit: capsule dry-out – J. Edwards et al., spore dispersal – J. Edwards et al. 2010; research credit: J. Edwards et al.)
Our bodies are filled with a network of blood vessels responsible for keeping our cells oxygenated and carrying away waste products. In many ways, our blood vessels are tiny pipes, but there’s a crucial difference in the flow they carry: it’s pulsatile. Because the flow is driven by our hearts, rather than a continuous pump, every heartbeat creates a distinct cycle of acceleration and deceleration in the flow. And new research has found that this cycle, when combined with curvature or flow restrictions like plaque build-up, can create turbulence in unexpected places.
Specifically, the researchers found that decelerating pipe flows can develop a helical instability that breaks down into turbulence, even in vessels where purely laminar flow would be expected. In the animations above, you can see the flow slow, develop swirls and then break into turbulence. The flow becomes laminar again as it accelerates, but during that brief bout of turbulence there’s much higher forces on the walls of a blood vessel. Over time, that extra force could contribute to inflammation or even hardening of the arteries. (Image and research credit: D. Xu et al.; via phys.org)
