Showing posts with label defense. Show all posts
Showing posts with label defense. Show all posts

Sunday, September 8, 2019

Tiny Ninjas, Big Bites (A Guest Post)

By Alexis Brauner

Venom isn’t just a weapon for snakes and spiders.

A smaller, more dangerous insect is in existence and falls into the realm of venomous creatures: the assassin bug. This little critter is part of a scientific family called Reduviidae, a group where all the members share the same characteristic of being an ambush predatory bug. They prey on invertebrates (animals that don’t have a spine), such as crickets and mealworms, by injecting venom into them.

An assasin bug. Source: Fir0002/Flagstaffotos at Wikimedia Commons.

Assassin bugs are believed to have two versions of venom – one for feeding and one for defense. Both types of venom are made up of more than 100 proteins, but what is unique about it is its ability to paralyze and liquify the inside of the prey. That’s right… liquify. The tissues of the prey turn into a jello-like substance that the assassin bug can then suck through a long tube on its mouth called the proboscis.

How is the venom able to do that?

First, let’s peek at the mechanisms that work to carry the venom through the body of the assassin bug and into its meal.

The venom apparatus of an assassin bug is made up of three main parts: secretory glands, a muscle-driven pump, and a venom channel. The three secretory glands (the anterior main gland, posterior main gland, and accessory gland) are in the thorax and abdomen of the assassin bug. These separate glands release a specific form of assassin bug venom depending on what situation the bug is facing. For example, the anterior main gland releases a form of venom that does not paralyze prey but is thought to be used as a defense mechanism, while the posterior main gland releases the deadly form of venom.

The venom apparatus of an assassin bug. Source: Walker, et. al, 2018, modified by Alexis Brauner

Once released, the venom then makes its way to a muscle-driven pump within the head of the bug. The pump fills with the available venom when the muscle contracts and is released once the muscle relaxes. Think of the venom pump as a clothes pin: when you push on the prongs, the pin opens, and you can put things in it to hold; once you let go of the prongs, the mouth of the pin closes, but now the prong end is open. In this example, your fingers are the muscle and the clothes pin is the pump with one end open at a time. The muscle relaxation releases the venom into the venom channel in the interlocking maxillary stylets (also known as the fangs) of the assassin bug. And then…

BOOM!

Venom is in the food or the foe.

And if it’s in the food, then the tissues of the prey turn into liquid. This liquification phenomenon is caused by enzymes in assassin bug venom called proteases. All enzymes catalyze, or speed up, chemical reactions; however, proteases are specialized enzymes that catalyze the destruction of proteins. This means that the assassin bug venom goes into the prey and the proteases are like Pac-Men with razor sharp teeth that grind up the primarily protein tissue at such a lightning fast speed that, within seconds, the prey is juice!

Scientists continue to research assassin bug venom to learn more about its components, but one thing is for sure: The extraordinary liquid weapon housed in such a small insect is why assassin bugs are tiny ninjas with big bites.


To learn more:

Walker, A., Madio, B., Jin, J., Undheim, E., Fry, B., King, G. (2017). Melt With This Kiss: Paralyzing and Liquefying Venom of The Assassin Bug Pristhesancus plagipennis (Hemiptera: Reduviidae). Mol Cell Proteomics, 16 (4), 552-566. DOI: 10.1074/mcp.M116.063321.

Walker, A., Mayhew, M., Jin, J., Herzig, V., Undheim, E., Sombke, A., Fry, B., Meritt, D., King, F. (2018). The assassin bug Pristhesancus plagipennis produces two distinct venoms in separate gland lumens. Nat Commun, 9, 755. DOI: 10.1038/s41467-018-03091-5

Friday, August 30, 2019

A Tiny Surprise in Regards to Regeneration (A Guest Post)

A reposting of an original article by Jessica Klein in The Scorpion and the Frog.

The ability to regenerate limbs and tails is nothing new to reptiles and amphibians. Many lizards are able to drop their tails to escape an enemy, whereas salamanders have been known to grow back entire legs with muscle after being attacked by a predator. These regenerative characteristics have been seen to some extent in rabbits and pika before 2012, but were later discovered to occur extensively in, surprisingly enough, small African spiny mice.

One of the African spiny mouse species. Photo by Ashley Seifert and Tom Gawriluk.

In a study done by Ashley W. Seifert and Megan G. Seifert at the University of Kentucky, Todd M. Palmer and Malcolm Maden at the University of Florida, Stephen G. Kiama at the University of Nairobi, and Jacob R. Goheen at the University of Wyoming, African spiny mice were studied in order to view the extent of their regenerative properties, why they might occur, and the physiological processes that make it happen.

The rodents were captured in Kenya, where researchers learned that vigorous movement during handling caused the skin of African spiny mice to come apart. One mouse was reported to have an open wound that took up 60% of its back, just from being handled! Therefore, Dr. Seifert measured the amount of strength it took to tear the skin of spiny mice using something called a Hounsfield tensometer. He took the measurements from that tool and graphed them on a plot, creating something called a stress-strain curve which showed how much strength it took to tear the skin of the mouse.

The strength measurements revealed that the skin of these species was 77 times weaker than average mice, explaining why their skin tore so easily during the handling process. In order for the African spiny mice to survive such large injuries due to their extremely fragile skin, it would be beneficial to heal quickly or regenerate the skin. This is exactly what Dr. Seifert discovered.

An African spiny mouse shows
the regenerative process with
(1) being before the wound
(2) being after the wound and
(3) showing how the wound was
completely healed after 30 days.
Figure from Seifert, et al., 2012.
After the strength measurements were completed, the rodents were anaesthetized and had 4mm and 1.5cm wounds made on their skin, as well as 4mm holes punched in their ears in order to view the regeneration process. In an average rodent, the repair of a 4mm skin wound takes around 5 to 7 days and is accompanied by a significant amount of scarring. However, in the African spiny mouse it only took 1 to 2 days for scabbing of the skin wound to occur with new cells forming on the outside of the wound to repair it. After just 10 days, the ear of the mouse was fully healed. In the ear punches, there were no signs of scarring that would have been expected in a rodent, and healthy cartilage had formed. By the 21st day of the experiment, African spiny mice had developed new hair follicles and healthy new hair covering the once wounded area. In total, Dr. Seifert discovered that African spiny mice were capable of regenerating their skin, hair follicles, and sweat glands.

Dr. Seifert suggested the skin of African spiny mice is fragile because it allows them to escape predators. This would require a quick healing time to reduce the chance of infection and ultimately death in the mouse after escaping. This is why they may have gained the ability to regenerate their skin, but how exactly does this happen? Dr. Seifert and his research team recently showed that, in these species, it occurs through a process known as epimorphic regeneration. This is when a blastema (a mass of immature, unspecialized cells) forms where the wound once was. These cells are capable of turning into whatever type of tissue was present in that area. This particular method of regeneration is how salamanders are capable of regenerating their limbs. Again, more research would need to be done in order to confirm or deny this. However, one thing is true, and that is that more research into this could prove to be useful in the future of medicine when it comes to healing critical and invasive injuries. By discovering the physiological process behind this, and then being able to replicate it in a lab, researchers may discover ways to heal injuries faster.




Works Cited

Seifert, Ashley W., Stephen G. Kiama, Megan G. Seifert, Jacob R. Goheen, Todd M. Palmer, and Malcolm Maden. "Skin Shedding and Tissue Regeneration in African Spiny Mice (Acomys)." Nature 489 (2012): 561-65. doi:10.1038/nature11499

Gawriluk, Thomas R., Jennifer Simkin, Katherine L. Thompson, Shishir K. Biswas, Zak Clare-Salzler, John M. Kimani, Stephen G. Kiama, Jeramiah J. Smith, Vanessa O. Ezenwa & Ashley W. Seifert. "Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals" Nature Communications 7.11164 (2016). doi:10.1038/ncomms11164

Tuesday, July 5, 2016

A Tiny Surprise in Regards to Regeneration (A Guest Post)

By Jessica Klein

The ability to regenerate limbs and tails is nothing new to reptiles and amphibians. Many lizards are able to drop their tails to escape an enemy, whereas salamanders have been known to grow back entire legs with muscle after being attacked by a predator. These regenerative characteristics have been seen to some extent in rabbits and pika before 2012, but were later discovered to occur extensively in, surprisingly enough, small African spiny mice.

One of the African spiny mouse species. Photo by Ashley Seifert and Tom Gawriluk.

In a study done by Ashley W. Seifert and Megan G. Seifert at the University of Kentucky, Todd M. Palmer and Malcolm Maden at the University of Florida, Stephen G. Kiama at the University of Nairobi, and Jacob R. Goheen at the University of Wyoming, African spiny mice were studied in order to view the extent of their regenerative properties, why they might occur, and the physiological processes that make it happen.

The rodents were captured in Kenya, where researchers learned that vigorous movement during handling caused the skin of African spiny mice to come apart. One mouse was reported to have an open wound that took up 60% of its back, just from being handled! Therefore, Dr. Seifert measured the amount of strength it took to tear the skin of spiny mice using something called a Hounsfield tensometer. He took the measurements from that tool and graphed them on a plot, creating something called a stress-strain curve which showed how much strength it took to tear the skin of the mouse.

The strength measurements revealed that the skin of these species was 77 times weaker than average mice, explaining why their skin tore so easily during the handling process. In order for the African spiny mice to survive such large injuries due to their extremely fragile skin, it would be beneficial to heal quickly or regenerate the skin. This is exactly what Dr. Seifert discovered.

An African spiny mouse shows
the regenerative process with
(1) being before the wound
(2) being after the wound and
(3) showing how the wound was
completely healed after 30 days.
Figure from Seifert, et al., 2012.
After the strength measurements were completed, the rodents were anaesthetized and had 4mm and 1.5cm wounds made on their skin, as well as 4mm holes punched in their ears in order to view the regeneration process. In an average rodent, the repair of a 4mm skin wound takes around 5 to 7 days and is accompanied by a significant amount of scarring. However, in the African spiny mouse it only took 1 to 2 days for scabbing of the skin wound to occur with new cells forming on the outside of the wound to repair it. After just 10 days, the ear of the mouse was fully healed. In the ear punches, there were no signs of scarring that would have been expected in a rodent, and healthy cartilage had formed. By the 21st day of the experiment, African spiny mice had developed new hair follicles and healthy new hair covering the once wounded area. In total, Dr. Seifert discovered that African spiny mice were capable of regenerating their skin, hair follicles, and sweat glands.

Dr. Seifert suggested the skin of African spiny mice is fragile because it allows them to escape predators. This would require a quick healing time to reduce the chance of infection and ultimately death in the mouse after escaping. This is why they may have gained the ability to regenerate their skin, but how exactly does this happen? Dr. Seifert and his research team recently showed that, in these species, it occurs through a process known as epimorphic regeneration. This is when a blastema (a mass of immature, unspecialized cells) forms where the wound once was. These cells are capable of turning into whatever type of tissue was present in that area. This particular method of regeneration is how salamanders are capable of regenerating their limbs. Again, more research would need to be done in order to confirm or deny this. However, one thing is true, and that is that more research into this could prove to be useful in the future of medicine when it comes to healing critical and invasive injuries. By discovering the physiological process behind this, and then being able to replicate it in a lab, researchers may discover ways to heal injuries faster.




Works Cited

Seifert, Ashley W., Stephen G. Kiama, Megan G. Seifert, Jacob R. Goheen, Todd M. Palmer, and Malcolm Maden. "Skin Shedding and Tissue Regeneration in African Spiny Mice (Acomys)." Nature 489 (2012): 561-65. doi:10.1038/nature11499

Gawriluk, Thomas R., Jennifer Simkin, Katherine L. Thompson, Shishir K. Biswas, Zak Clare-Salzler, John M. Kimani, Stephen G. Kiama, Jeramiah J. Smith, Vanessa O. Ezenwa & Ashley W. Seifert. "Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals" Nature Communications 7.11164 (2016). doi:10.1038/ncomms11164

Monday, November 2, 2015

Body Armor is Not Always for Protection

When we see an animal covered in scales and plates, we assume that it has this armor to protect itself from predators. It seems obvious, which is probably why scientists had not really tested it… until now. And they found that it is not necessarily true.

An armadillo girdled lizard has some impressive body armor, but does it do what we think it does?
Image by Handre Basson at Wikimedia Commons.
Today at Accumulating Glitches, I talk about new research on the functions of plates and scales in cordylid lizards. Check it out here.

And to learn more, check this out:

Broeckhoven, C., Diedericks, G. and le Fras Mouton, P. What doesn’t kill you might make you stronger: functional basis for variation in body armour, Journal of Animal Ecology, 84, 1213–1221 (2015). DOI: 10.1111/1365-2656.12414.

Monday, August 24, 2015

The Weirdest Animals on Earth: 12 Amazing Facts About Octopuses


Photo of a day octopus by
Ahmed Abdul Rahman available
at Wikimedia Commons.
1. The plural of octopus is octopuses. How an English word is pluralized depends, in part, on its origins. Latin words that end in –us are generally pluralized by replacing the –us with an –i (the plural of alumnus, for example, is alumni). But octopus is not Latin – It comes from the ancient Greek word októpous, whose plural is októpodes. Although octopodes is technically correct, since it has been adopted into the English language, the word is now pluralized in the English way, making it octopuses. So octopi is commonly used but not technically correct, octopodes is technically correct but not commonly used and octopussies is just plain wrong.

2. Octopuses are mollusks. This means that they are not only closely related to squid and cuttlefish, but also to clams, oysters, snails and slugs.

3. Octopuses are crazy-smart. They can solve problems, learn from watching others, use tools, and remember experiences. They even have personalities and play with toys. Check this out:



4. Octopuses have nine brains! Rather than a large centralized brain like ours, octopus brains are more like the internet. Their main CPU is a fairly small brain in their head, but each of their eight arms has an additional brain of its own. In fact, two-thirds of an octopus’ neurons are in the arms, which can independently attach to things, push things, and even smell things. They can even react after they have been severed! Not only that, but their severed arms recognize their previous owner:



5. If an octopus loses an arm, it can grow back. Those crazy arms are like the brooms in Disney's Sorcerer's Apprentice in Fantasia!

6. Octopuses are amazing camouflage artists. Their soft bodies can squeeze into ridiculously small cracks and crevices and take on any number of shapes. A 50-pound octopus, for example, can squeeze through a 2-inch hole! They can also change the color and texture of their skin to match their background.


The mimic octopus, the ultimate master of disguise, doesn’t just imitate their background, but also flounders, starfish, poisonous lionfish, and sea snakes.



A vertebrate eye (left) versus an octopus eye (right).
1: Retina, 2: Nerve fibers, 3: Optic nerve, 4: Blind spot.
Image by Jerry Crimson Mann at Wikimedia.
7. Octopuses don’t have visual blind-spots. Most animal eyes detect light patterns when light travels to the retina (the layer in the back of the eye) and falls on photoreceptor cells, causing the cells to send electrical signals through the optic nerve to the brain. Vertebrate photoreceptor cells face backwards, so their nerve fibers come in front of the retina and then exit the eye together through the optic nerve, creating a small region in the back of the eye with no photoreceptor cells. If light falls on this spot, we literally will not see it, although our brain will compensate for this missing light by imagining what should be there based on the rest of what we see. We call this our blind spot. You can test your blind spot by closing your left eye and focusing your right eye on the “R” below. Move your face towards or away from the screen until the “L” disappears. You can test your left eye by staring at the “L” in the same way.
In octopus eyes, the photoreceptor cells face forwards and the nerve fibers go behind the retina. This means that they have a continuous layer of photoreceptor cells and no blind spot.

8. Octopuses are more blue blooded than police officers. Their blood is truly blue, due to the fact that they don’t have hemoglobin, our respiratory pigment that contains iron and turns red when it binds to oxygen. Rather, they have hemocyanin, which contains copper and turns blue when oxygen binds to it.

9. Octopuses have three hearts! They have two small hearts that each pump blood through the gills and a main systemic heart that collects the blood and pumps it through the circulatory system.

10. Octopus ink is a defensive chemical concoction. It not only obscures the view of an attacker, but it also contains a chemical that irritates the predator’s eyes and temporarily paralyzes its sense of smell.

11. Octopuses bite with a bird-like beak and venomous saliva, which is mostly used to subdue prey. Of the approximately 300 octopus species, only the small blue-ringed octopus is known to be deadly to humans.

12. Octopuses die after they mate for the first time. And they mate in an odd way too: males use the tip of their third arm on the right to either insert their spermatophores (sperm packets) directly into the female’s tubular breathing funnel or he just hands it to her (The tip of the third right arm can be used to tell if an octopus is male or female). If he hands it to her, she accepts it with one of her right arms (we don’t know why they’re right-handed this way). Then the males go off to die. The females eventually lay up to 400,000 fertilized eggs, although they can wait months before they do this. She tends them and guards them at the exclusion of all else until they hatch, at which point her body rapidly deteriorates as her cells die off.


Monday, July 6, 2015

Song Battles With Other Species Can Change Your Tune

Many animals defend territories from members of their own species for mating, breeding, and finding food and they often use species-specific vocalizations to do this. Defending a territory can be risky and costly in both energy and time, so even territorial animals generally don’t waste this effort on other species that do not share their same food and breeding needs. But what do you do if you live around another very similar species that has the same needs that you do? Can two species learn to speak each other’s languages to live in territorial harmony?

A common nightingale.
Photo by Frebeck at Wikimedia Commons.
A thrush nightingale.
Photo by Locaguapa at Wikimedia Commons.
Today at Accumulating Glitches, I tell the story of two species of nightingales and how they are learning to sing each other's songs to defend their territories! Check out the article here.

Monday, November 3, 2014

War and Peace


A group of Gelada baboons in Ethiopia.
Photo by A. Davey at Wikimedia Commons.
Syria and Iraq. Ukraine. The Gaza Strip. People are dying in large numbers at the hands of other humans, and for what? Land and resources? Is it really worth it? It is often said that humans are the only species so horrific as to kill its own species in war. But the fact is, we are not alone in what was previously thought to be a uniquely human trait. In many animal groups, individuals will band together in collective defense of territory and resources.

This week at Accumulating Glitches I talk about how group size influences the ability of primate groups to hold their territories. Check it out here.

And to learn more, check this out:

Willems, E.P. Hellriegel, B. and van Schaik, C.P. The collective action problem in primate territory economics, Proceedings of the Royal Society B, 280: 20130081 (2013). DOI: 10.1098/rspb.2013.0081.

Monday, October 13, 2014

Is That Lizard Possessed!? (A Guest Post)

By Tawny Liebe

Image from Chuck Heston on Flickr.
A creature straight from the depths of hell… or at least as close as you can get on this planet. The Texas horned lizard or “horny toad” is found in the deserts of the southwest United States and has an unusual adaptation to deter predation exclusively from a few species of canines. When threatened by coyotes, foxes, and dogs, the horned lizard squirts blood from its eyes to hit targets up to three feet away! A total of six species of horned lizard have been proven to respond this way to canine attack, while none have responded this way to other predators, such as the grasshopper mouse or the roadrunner. So what is the deal? How do they do this and how does it work as predator defense?

Veins have one-way valves
to prevent backflow.
Drawing by Tawny Liebe.

Before we get to that, there are a few things you need to know. First of all, the circulatory system includes a network of arteries and veins. Arteries carry blood full of oxygen to body tissues while veins carry blood that lacks oxygen from the rest of the body back to the heart. This means that for the blood, in someone’s foot for instance, to get all the way back to the heart through the veins, the blood must work against gravity. When you (or this lizard or many other species) move, blood is propelled from one chamber in the vein to the next until it reaches the heart. The blood is prevented from flowing back into the previous chamber by one-way valves, causing the blood to pool.

In order to squirt blood from their eyes, horned lizards manipulate the network of veins in their head so that they build up pressure, like a volcano getting ready to blow. By constricting a pair of throat muscles unique to reptiles, they effectively close their jugular veins and increase the blood pressure in their head. This is thought to be enhanced by another pair of muscles between the jugular veins and the eyes that help increase the blood pressure in the head even further, causing the blood to move into the sinuses of the eyes. The pressure continues to build until the blood breaks through the wall of the eye socket into the eyelids where it is forced into the tear duct and erupts like a Mentos in a Coke bottle all over whatever is chomping at the poor little lizard.

As if these lizards couldn’t get any more amazing, recent studies have shown that it is actually a compound in their blood that canines don’t like. Scientists have also found that this chemical is in their circulating blood, not just the blood that is squirted from their eye, rejecting an earlier hypothesis that the chemical is picked up in the tear duct. To top off all of this awesomeness, the chemical may be acquired through its main food source- harvester ants, which are venomous. These ants aren’t actually a requirement of the horned lizard’s diet and yet they are specialized to eat them. The horned lizard’s blood plasma binds to the venom, which neutralizes its toxicity and the resulting compound may be what deters these canines.

Now that we know how horned lizards are capable of this type of defense and how they most likely make their blood so undesirable, what is it about this chemical that is so appalling to these predators? It appears that the target area of the blood is the mouth since the horned lizard only squirts the blood when the canine begins to bite down on its head. This suggests that it may be the taste of the blood that prevents the horned lizard from becoming that coyote’s tasty snack.

The horned lizard’s ability to squirt blood at canines to prevent their untimely death is truly amazing and complex and there is still much to learn about it. Their ability makes me wonder how many other cool anti-predator adaptations there are out there in the animal and even the plant kingdom! Below is a video that will allow you to appreciate the full effect of this awesome defense strategy, enjoy!




References:

Heath, J.E. 1966. Venous shunts in the cephalic sinuses of horned lizards. Physiological Zoology 39(1): 30-35.Middendorf, G.A. and Sherbrooke, W.C. 1992. Canid elicitation of blood-squirting in a horned lizard (Phrynosoma cornutum). Copeia 1992(2): 519-527.

Middendorf, G.A. and Sherbrooke, W.C. 1992. Canid elicitation of blood-squirting in a horned lizard (Phrynosoma cornutum). Copeia 1992(2): 519-527.

Middendorf, G.A. et. al. 2001. Comparison of blood squirted from the circumorbital sinus and systemic blood in a horned lizard, Phyrnosoma cornutum. The Southwestern Naturalist 46(3): 384-387.

Middendorf, G.A. and Sherbrooke, W.C. 2004. Responses of kit foxes (Vulpes macrotis) to antipredator blood-squirting and blood of Texas horned lizards (Phrynosoma cornutum). Copeia 2004(3): 652-658.

Sherbrooke, W.C. 1992. Chiricahua Mountains Research Symposium. Horny “toad” tales from the Chiricahua mountains as, told by a biologist. Southwest Parks and Monuments Association, Tuscon, AZ. 78-80.