Showing posts with label tropism. Show all posts
Showing posts with label tropism. Show all posts

When Is A Chloroplast Not A Chloroplast?

Biology concepts – gravitropism, plastid, chloroplast, chromoplast, amyloplast, leucoplast, malaria parasite

Believe it or not, the way plant roots know to grow into the dirt is related to photosynthesis! “How can this be?” you ask. Well, let’s talk about it.

The cells in the tips of the plant rootlet respond positively to gravity, called gravitropism(the older word for it is geotropism). If you lay a growing plant on its side, the roots will respond by growing (turning) toward the gravity within 10 minutes. The mechanism for this stimulation involves tension and a plant hormone called auxin.

Auxin is a growth hormone that gets redirected
in the growing plant root. The statoliths settle
and trigger the hormone to some cells more than
others. Auxin means ”to grow” in Greek, but in
some cases, like in gravitropism of roots, it
actually inhibits growth.
The rootcap (the cells at the tip of the root) have some specialized cells called statocyte (stat = position, and cyte = cell). Inside the statocytes are dense granules called statoliths (lith = stone). The statoliths are made of densely packed starch and are a specialized type of organelle called an amyloplast, which is used in many plant cells for storing carbohydrate in the form of starch (amylo = starch). The statoliths are denser than the cytoplasm of the cell; they don’t just float around, they settle out according to gravity.

Since the statoliths are connected to the membrane of the cell by the cytoskeletal actin molecules, so when they settle toward gravity, some cells in the membrane are stretched and some are compressed. This tension signals the cells to change the number of receptors for the growth control hormone auxin. More tension (more stretch) causes the auxin to move away, toward cells that are under less tension. Auxin prevents cell enlargement and cell division, so those root tip cells on the bottom receive more inhibition. Those on top enlarge more and divide more, so the root turns down. If the root is already vertical, the tension is equal in all directions, and the growth is equal in all directions – the root gets thicker and longer.

Gravitropism is related to photosynthesis in that both mechanisms involve chloroplasts, sort of. Root cells don’t perform photosynthesis, they are underground, so they don’t have chloroplasts. But they do have the amyloplastid statoliths, and these are related to chloroplasts.

Both amyloplasts and chloroplasts are specialized versions of the plant organelle called the plastid. We asked last week about what defines a plant cell – maybe the plastid is it. All plant cells have some plastids, but in different plant cells they may take different forms, including chloroplasts, chromoplasts, leucoplasts, amyloplasts, elaioplasts, or proteinoplasts, but they all start out as proplastids (pro = early and plastos = form in Greek).

Proplastids are in every new plant cell. From there
they can differentiate into other forms, including
the chloroplast. Other plastids are used for storage
or biochemical production. We will talk about statoliths
again when we discuss proprioception.
When acell divides, each daughter gets its share of proplastids, and then depending on the chemical signals that the daughter cell receives, the proplastid will differentiate (from latin, means to make separate) into the types of plastids that the cell needs. A proplastid can become any type of plastid, and from time to time can change between forms as the plant cell requires. Think of it as a sort of stem cell inside a plant cell – if the cell happens to be in the stem of the plant, it could be a stem cell inside a stem cell!

Proplastids become etioplasts, chloroplasts or leucoplasts. The etioplast is a sort of pre-chloroplast; a chloroplast without chlorophyll. It is waiting to be stimulated by light energy before it decides to spend all the energy it requires to make the chlorophyll. The old science fair project about growing bean plants in the dark demonstrates the etioplasts. The plants are white when grown in the dark, but bring them into the light and they soon green up. The sunlight stimulates the etioplasts to make chlorophyll, become full-fledged chloroplasts and start photosynthesizing.

This is a photomicrograph of the plastids of a
red flower petal. The chromoplasts hold the
xanthocyanin pigments, but we see it as a
continuous color because they are so small.

If the proplastid does not differentiate toward a chloroplast pathway (etioplast too) then it will become a leucoplast (leuko = white). The leucoplasts don’t have color; they become specialized for the storage of plant materials. If they store starch, they are called amyloplasts. Lipid storing leucoplasts are called elaioplasts, while protein storing plastids are called proteinoplasts. Each type serves a crucial purpose in the cells they inhabit, and they can all interchange, depending on the conditions the plant cell finds itself in.

Even more important, leucoplasts that are not serving as storage organelles have biosynthetic functions. They work in the production of fatty acids and amino acids. Amino acids link together to from proteins, so their synthesis is very important for plants. Plants must manufacture every amino acid it needs, whereas we get many of ours in our diet. There are even some amino acids that humans can’t make, called the essential amino acids. Of the twenty common amino acids, nine of them must be taken in through our diet, and some people with pathologies can’t make up to seven more. Plants don’t have this luxury; all their amino acids must be made on site. Good thing they have leucoplasts.

There is one other type of plastid that we haven’t talked about, the one that is important for the Autumn tourist trade. Etioplasts and chloroplasts can differentiate into chromoplasts, organelles that store pigments (colored molecules) other than chlorophyll. Chlorophyll provides energy through photosynthesis, but they also have a cost. The old saying, “It takes money to make money” applies to plants as well. It takes energy to make chlorophyll, so it only pays to make chlorophyll when there is ample sunlight to put through photosynthesis. When the days get shorter, the profit margin for producing chlorophyll goes down, so the plant just stops making it.

Twin females were imaged after a lifetime of smoking or non-smoking.   
Can you guess who was exposed to the oxygen radicals in cigarette
smoke her whole adult life?
The oxygen produced in plant cells during photosynthesis can damage many molecules; oxygen likes to react with other compounds and steal or donate electrons. This oxidative damage can wreak havoc with the cells, just look at the face of a long time smoker – the damage and aging process from the oxidants in cigarette smoke will be evident. The chromoplast pigments, like carotenoids (oranges and yellows) and xanthocyanins (reds and purples), can serve as antioxidants, and protect the other cell structures from the damaging effects of oxygen.

So the chloroplasts lose their chlorophyll in autumn and could be called leucoplasts, but the chromoplasts still have the pigments that had been masked by the greater number of chlorophyll molecules. The trees turn magnificent colors and bring people from the cities to stay in bed and breakfasts, and to purchase handmade scarves and way too much maple syrup and apple butter. Economy and biology are so often interrelated.

Plastids are the quintescential plant organelles – no plant cell is without them in some form (well O.K., there is one exception, we’ll talk about that next week). But that still doesn’t mean that they define a plant cell. Remember that algae are not plants, but they have chloroplasts, and chloroplasts are one type of plastid. There is even a bigger exception in this area; some of the apicomplexans.

Certain protozoal organisms, including the malaria parasite (Plasmodium falciparum) contain an organelle called an apicoplast. P. facliparum or its ancestor obtained an algae cell by secondary endosymbiosis (the primary endosymbiotic event was the algae taking in a cyanobacterium), so the apicoplast has a four, not two, membrane system.

The apicoplast of the malaria parasite is of plastid
origin, but it undergoes some unplant-like changes
during cell division. Image D with the branched
apicoplast is my favorite. Those in panel F will
grow to look the one in panel A.
The apicoplast does not perform photosynthesis; we aren’t exactly sure what it does – but it is crucial for the survival of the parasite. It is located in the front of the parasite (in the direction it moves and invades cells) and is always close to the nucleus and the mitochondrion. This suggests some role(s) in energy production and molecule synthesis.

There is evidence that the apicoplast works in fatty acid and heme synthesis, like the leucoplast or in the production of ubiquinones that are important for the electron transfer chain in the mitochondria. There is also evidence that it is involved in FeS cluster production, like the hydrogenosomeand mitosome. Both of these pieces of evidence show the interelationships of the endosymbiosed organelles and the connection between energy production and energy use. Whatever their functions are, if you destroy or inhibit it the malaria bug dies. As such, it has been a popular target for anti-malarial drugs.

Malaria parasites cured of their apicoplasts (cured means freed of) do not die right away. They just can’t invade any new cells and therefore can’t complete their life cycle. This is why anti-apicoplast drugs may be a boon to malaria treatment. The biosynthetic pathways in the apicoplast are the targets of four recent drugs, but the primary way to stop malaria remains the mosquito net. There is strong hope that a new vaccine, called RTS,S is a light at the end of the tunnel for this killer of millions.
The melanosome and the plastid have more in common.
The very rudimentary eye of some dinoflagellates
(dinos = rotating, and flagellum = whip) has a melanin-like
molecule in the pigment cup and the structure is called a
melanosome. However, it is of plastid orgin. The picture
above is of Polykrikos herdmanae. It has 8 transverse flagella,
as well as the pigmented eyespot to detect light sources.


One final thought on the plastid – an addition to the exception of melanosomes. We discussed a few weeks ago that melanosomes were the only organelles that could move from cell to cell. Well, that isn’t exactly so. I held off on adding the plastid to that list until we had discussed what a plastid was.

A 2012 study at Rutgers University tested whether plastids and mitochondria could move between plant cells. There results showed that entire plastid genomes could be seen in recipient cells, and the fact that the whole chromosome passed indicated that the plastid was probably moving from cell to cell intact. But there was no movement of the mitochondria, so it is a plastid (and melanosome) specific event.  The researchers hypothesize that this may be a way for plant cells to repopulate damaged cells with working organelles. As such, it would be similar to how mammalian stem cells can move mitochondria into damaged cells during tissue repair. But that is another story.

We have repeatedly talked about how the mitochondrion and plastid can replicate on their own and then are portioned out to the daughter cells when a parent divides. Can it really be that simple? I’ll bet there is a definite mechanism, and I bet that mechanism has exceptions. Let’s look into this next time.

Gregory Thyssena,Zora Svaba, and Pal Maligaa (2012). Cell-to-cell movement of plastids in plants Proc Natl Acad Sci U S A. , 109 (7) DOI: 10.1073/pnas.1114297109

For more information or classroom activties on plastids, gravitropism, or Plasmodium falciparum see:

Plastids –

Gravitropism –
207.62.235.67/case/biol215/docs/roots_gravity.pdf

Plasmodium falciparum

Plants That Don’t Sleep Will Take The Dirt Nap

Biology concepts – nastic movements, turgor pressure, evolutionary pressure, tropism, osmosis

If you don’t let a Mimosa pudica (sensitive plant) plant rest at night, it will wilt away to nothing. A plant that needs a good night’s sleep? Really? We have talked about how sleep revitalizes different brain functions, especially within the hypothalamus (The Best Cure For Insomnia Is To Get A Lot Of Sleep), but plants don’t have a hypothalamus or any brain for that matter. So why does it die if it can't rest; is it out of its mind?


The prayer plant on the left is how it looks during the day, but
on the right, the leaves have folded or curled up. They also stand
straight up, as if at attention. A tough way to spend the night, but
it must serve some purpose.
The prayer plant (Maranta leukoneura) folds up its leaves at night and tilts them upward. When morning comes, the leaves tilt back into their day position and unfold to catch as much sunlight as possible. The folded leaves might look like they are praying (hence the name), and it may appear that they are sleeping, but this is just anthropomorphism.

Humans have a need to feel connected to the rest of Earth’s life, and in the process, we tend to see the behaviors of other organisms in human terms, trying to assign some human motivation to them. So, is the plant sleeping? Does it need to rest? No. Sleep in animals implies inactivity and neural rearrangement, and these don’t occur in plants.


Charles Darwin performed crucial experiments
in plant movement in his later life, including the
identification that chemical signals moving in the
plant are responsible for growth toward the light
(heliotropism). Notice that his son got pretty good
billing as an assistant.
However, the fact that the plant carries out this activity every night suggests that it has evolved in response to some pressure, some need. Surprisingly little is known about why plants move their leaves at night, but there are a few hypotheses. Some scientists believe that changing the angle of the leaves helps funnel dewdrops and overnight rain down the trunk or stem to the roots. Charles Darwin published two books on these plant movements, his theory being that the behavior reduced the chance of chill or freezing.

Another hypothesis suggests that leaves fold up to keep the rain from pooling on them and promoting bacterial or fungal growth. Or perhaps, apposing one leaf closely to the opposite leaf reduces the amount of water lost overnight. However, aquatic plants don’t have to worry about loss of water, but some immersed plants, like Myriophyllum Mattogrossense, still fold up at night. It may be a holdover from their terrestrial days, as most of today’s aquatic plants evolved from terrestrial plants.

My personal favorite proposes that by folding up their leaves, the plants give nocturnal predators a better shot at seeing, hearing, and smelling nocturnal prey. By helping the predators, plants are indirectly protecting themselves from animals that would eat them- plants are sly little devils (more anthropomorphism). It is probable that different plants move for different reasons, so one hypothesis almost certainly won’t cut it for all organisms.

Plants have night moves other than folding leaves. Morning glories (Ipomoea violacea) close their flowers overnight. The reasons for this movement may be a little plainer. Dry pollen sticks to pollinators better than wet pollen, so closing off the stigma to rain or dew keeps the pollen dry. It also takes energy to maintain an open flower; this energy would be best spent when pollinators are around. If the plant’s pollinators are diurnal, they why leave the buffet open all night?


Just as animals have an internal clock, plants gauge
their movements according to the circadian period.
Often plants match their rhythms to pollinator animals
they depend on or to avoid the active periods of
predators. Anyway, I like the picture.
There are also flowers that have the exact opposite behavior, opening their flowers as the sun sets. Philodendron selloum (Is It Hot In Here Or Is It Just My Philodendron) is a classic example, with its spathe closing down in the early morning hours.

Moonflowers (Ipomoea alba) are another example.  At about 8:00 pm, the moonflower opens. A single flower can go from completely closed to fully open in less than a minute (http://www.moonlightsys.com/themoon/flower.html). The morning glories and the moonflowers are both of genus Ipomoea, but they have opposite behaviors – different pressures lead to different adaptations, even in closely related species.

These movements of plant structures are independent of the direction of the stimulus, ie. they are not following the sun or being blown by a particularly wind, so they are called nastic movements. Nyctinasty (nyc = night or darkness, nastic = firm or pressed close) is the specific movement of leaves or flowers in a daily pattern, open during the day and closed at night. If directed by the position of a stimulus, the movements are called tropisms (heliotropism, thigmotropism, gravitropism).


The left picture shows that changes in the pulvinus shape could affect the direction of the entire petiole and all the leaves, or individual leaves (like on the sensitive plant). The middle cartoon indicates that filling the central vacuole with water can change the shape of the cell, pushing in one or more directions. The right image shows just how the extensor cells on the bottom must be inflated to lift the petiole, while turgidity in the flexor cells makes the leaf drop.
Nyctinastic movements are accomplished by the flow of water in and out of specific cells in the pulvini (swellings, singular is pulvinus) at the base of the petioles (the stalk that attaches the leaf blade to the stem). It is not unlike our muscle movements in that there is an extensor and a flexor pair. When K+ and Cl- are pumped into the extensor cells on the bottom of the pulvini, they become hypertonic and water follows the ions through osmosis. This causes the extensor cells to swell due to increased turgor pressure.

Turgor pressure refers to the pressure of the cell contents against the cell wall. This increased turgor pressure at the bottom of the petiole pushes the leaf up. In an opposite fashion, night causes a movement of ions to the flexor cells on the top of the petiole. Water flows out of the extensors and into the flexors by osmosis, causing the stem to droop. Flowers and leaves open and close by the same movements, with the extensor and flexor cells located at their bases.

Turgor pressure is the same mechanism which causes the venus flytrap (Dionaea muscipula) to snap closed its jaws of death when an insect disturbs its trigger hairs. These hairs are located on the nectar laden, red lobes of the trap. Touching just one trigger hair doesn’t spring the trap, two must be displaced within 20 seconds of each other. This saves energy and unnecessary trap closings; each trap snaps shut only four or five times, then dies. If you thought the moonflower moved fast, check out the venus flytrap (http://www.youtube.com/watch?v=ymnLpQNyI6g). I’m just surprised we can’t hear the water shooting into the flexor cells!


The venus flytrap supplements its diet of water and carbon
dioxide with proteins from the insects it catches and digests.
The bright surface with nectar draws them in, where they trigger the
mechanosensor hairs. The magnified image on the right shows a
trigger hair with its hinge that transmits a signal to the pulvini to
swell quickly and snap the trap shut.
The trigger hairs are mechanosensors. The stimulus that trips the trigger and causes the flow of ions and water in the extensor and flexor cells of the hinge region is directionally irrelevant; therefore, the snapping shut of the trap can be considered a nastic movement. In this case, as with the sensitive plant (Mimosa pudica), the movement is called haptonasty (hapto = touch).

A small percentage of plants have nyctinastic movements, so they are an exception to the rule that plants don’t move actively, but even a small percentage means that thousands of species do have these movements. This many exceptions underscores the point that nyctinasty must perform an important function.

Just as humans with fatal familial insomnia die from a lack of sleep (An Infectious, Genetic Disease), the sensitive plant has a much shorter lifespan when nyctinasty is prevented. A plant hormone that stimulates leaf opening was identified in 2006. When given to plants continuously, it caused the leaves to remain open. When nyctinasty was prevented in this way, the leaves were noticeably damaged within a few days, and the plant was dead in less than two weeks. It may not be sleep, but whatever it is, it is just as important.

Some plants are open during the day and some are open at night, just as some animals are active during the day and some during the night. And just as plants adapt to a time schedule to promote survival, animal adaptations are crucial to life in the light or the dark. But that doesn’t mean that some organisms won’t throw us a curve, as we will discover next time.

Ueda, M. and Y. Nakamura. 2006. Metabolites involved in plant movement and ‘memory’: nyctinasty of legumes and trap movement in the Venus flytrap. Natural Product Reports, 23 (4): 548-557.

For more information, classroom activities or laboratories on nastic movements or turgor pressure, see:

nastic movements –

turgor pressure –

Is It Hot In Here Or Is It Just My Philodendron?

Biology concepts – thermoregulation, pollination, tropisms, flower structure, plant communication

In many ways, plants are “smarter” than people (forgive the anthropomorphism). We can change our environment to suit our needs or move to a better environment. But plants can’t flip the light switch, can’t buy a bottle of water to quench their thirst, can’t turn on the air conditioner, and can’t hire a truck and move all their stuff to a better place.


Plants can react to many physical signals. We can sense gravity, but they can
differentiate parts of themselves with gravity – roots grow towards gravity
(positive geotropism) and stems grow away from gravity (negative geotropism).
So what can plants do given these limitations? They can make their own food (photosynthesis) – they’ve got us beat right there. They can turn to face the light (phototropism) or the sun (heliotropism). These abilities were explained by none other than Charles Darwin and his son in an elegant series of experiments in 1880.

Plant stems can grow away from gravity (negative geotropism or gravitism), while their roots grow toward gravity (positive geotropism) or water (hydrotropism). Finally, plants can twist around a wire and hold on (thigmotropism). Pretty talented, wouldn't you say? 

But wait, there's more. Plants can also communicate with one another. They alter their biochemistry to become less appealing to predatory insects or microorganisms, and their responses become better with each attack. After they develop a good defense for a particular predator, they will warn nearby members of the same species via dispersed chemicals. The warned plants then generate the best defense the first time they are attacked.

Plants can also recognize kin – and be nice to them. Research shows that plants grow less aggressively when surrounded by seedlings from the same mother plant compared to when surrounded by non-kin competitors. I wish I could get my kids to act that nicely towards one another.

Plants also commune with animals. The acacia tree has an arrangement with the ants that live on it. The tree produces hollow thorns for the ants to live in, and produces food for them to eat. In exchange, the ants protect the plant from predators such as caterpillars by attacking them. The ants will also prune away dead leaves and destroy nearby plants that might compete with their tree for light.


The acacia tree provides hollow thorns for ants to live in; the tree’s wood is so hard
that the ants can’t hollow it out on their own. The acacia wood was once used as nails. 
The acacia is related to the mimosa (sensitive plant) we discussed previously.
This is a great arrangement for both ant and tree (symbiotic mutualism), but becomes tricky during pollination. The ants will attack any insect that touches their tree; even potential pollinators.  So the acacia produces a chemical at the flower when an insect lands to feed on the nectar; it says, “this guy is O.K., don’t kill him.” Amazing - I can’t get the cats to come when I call them - and I feed them! Maybe saying someone is as dumb as a potted plant isn’t much of an insult.

Plants may be “smart” about temperature as well. They don’t regulate their own heat, and are usually the same temperature as the surrounding environment. Remember from the last post that it takes lots of energy to be an endotherm, so ectothermic plants enjoy great energy savings by adopting room temperature as their own.

A few plants can spike their temperature for a short time, usually to attract pollinators, but they can’t regulate the temperature. It is like setting a fire; it burns at as high a temperature as the fuel will allow, and then goes out.


P. selloum grows in tropical environments, but can
be found as a landscape planting in Georgia, the
Carolinas, and the gulf coast. It can grow 8 meters
(26 ft) tall and the leaves can be 1 meter (3 ft) in width.
Our exception to the rule of plant ectothermy is the philodendron. Many species of this genus can raise their temperature during the period when they produce pollen, and can regulate that temperature over a short period of time (2 days). The species Philodendron selloum (P. selloum, also called Philodendron bipinnatifidum, split leaf philodendron, tree philodendron) has been the most studied and will serve as our model.

P. selloum flowers in a structure called an inflorescence. This consists of a covering spathe and a spadix in the center. The flowers are located on the spadix, with a specific arrangement of male and female flowers, making the philodendron a monoecious plant (male and female on same plant). However, the flowers are incomplete, since each individual flower has only the male (pollen producing stamen) or female (ovule containing pistil) organs.


The flower of P. selloum is about 25 cm (10 in)
tall and the flowers are plain white, as it does
not use color to attract pollinators.
The male flowers are located on the top half of the spadix, while the middle region contains sterile male flowers, and the female flowers are located at the base. This arrangement, with the sterile gap in the middle, decreases the chances that the pollinators will pollinate a female flower on the same plant (self-pollination).

Self-pollination reduces genetic diversity as the offspring are clones of the parent (we will talk more about this next time). Also to help prevent self-pollination, the male flowers produce pollen in the first evening of the anthesis; the time period when the flower is open and fully functional. The female flowers can receive pollen on the second evening.


The spadix can reach and hold temperatures of 45 ˚C (113˚F)
and is most concentrated in the sterile male flowers. The female
flowers don’t produce heat, as this would damage the ovules.
P. selloum raises the temperature of the spadix, specifically the male flowers. The attractant is a female beetle sex pheromone that makes male beetles of a specific species think that potential mates are on this particular flower. To maximize the effect of the pheromone, the increased temperature of the spadix volatilizes the chemical (evaporates it into the air) so it can spread a greater distance. The beetles just follow their nose back to the correct plant!

The heat comes from a special reaction within the plant. Photosynthesis is actually an endergonic (energy consuming) reaction, it eats up heat, leaving the plant cooler. But respiration (creating ATP from the carbohydrates of photosynthesis) is exorgonic (heat releasing). These two processes are basically a wash, so P. selloum needs another way to generate the heat for the spadix.

Moreover, the P. selloum heat production must correlate to the time when the pollen is mature, must be localized to the spadix, and must be regulated. To do this, the philodendron has independently evolved the same trick that human babies use to stay warm!

Babies have a big surface area compared to their volume, so they tend to lose heat rapidly. This is why parents dress babies warmer than they dress themselves. To generate more heat, babies have brown fat (brown adipose tissue or BAT). BAT has more mitochondria than regular adipose (fat) tissue, and the iron in the mitochondria make this fat appear almost brown in color. The increased mitochondrial number helps to generate more heat as the fat is metabolized.

Fat is metabolized to generate heat instead of carbohydrates because it has more energy. Fat carries almost 9 kcal/gm, while carbohydrates contain only 4 kcal/gm. This is also why fat is used to store energy, it would take more than 2.5x the volume to store the same energy if it were all in the form of carbohydrate, especially since carbohydrates are connected with water when stored, while fats are not. Being fat is actually the most compact way to store energy.


Brown adipose tissue (BAT) has a centrally located nucleus and
several small lipid droplets in order to make room for the many
mitchondria. On the right, white fat cells have an offset nucleus
and are completely filled with a single lipid droplet.
To really up the heat ante, the mitochondria have an uncoupling protein (UCP) that disconnects the burning of fat from the generation of ATP. Instead of putting some of the energy into making ATP, all the energy is put toward giving off heat. Since babies aren’t coordinated enough to exercise to increase heat, and shivering isn’t that efficient, this non-shivering thermogenesis (NST) is their way to stay warm.

It was thought that adults didn’t have BAT, but recent studies indicate that most adults have some, and some people have a lot. BAT generation can actually help keep you thin, because the BAT is more readily metabolized –regular fat is a guard against bad times and the body holds on to it tightly, but BAT it is meant to be burned. New research suggests that chronic cold can stimulate BAT development, so forget your winter coat and just freeze your way into that size two.

P. selloum has developed BAT as well, an excellent example of convergent evolution (unrelated organisms develop similar characteristics). Plants use the alternative oxidase protein to uncouple fat metabolism from ATP generation instead of UCP, but the process is nearly the same. Using non-shivering thermogenesis, P. selloum can raise the temperature of the spadix to 104-113˚F and hold it there.

More amazing, P. selloum can somehow sense the ambient temperature and keep the spadix temperature 20-30˚F above that of the environment during that first evening. During the second day, the temperature is held around 80-95˚F, but is not controlled so stringently. The second evening sees a slow, regulated decrease in temperature to ambient by the third morning. It's a complex mechanism, but the payoff is survival of the species.

The whole thing is pretty smart for a plant, or for any organism. Next time, we will investigate the relationship between the pollinator beetle and P. selloum, and how limiting pollination to one species of beetle breaks a rule.

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For more information, classroom activities, or laboratories on tropisms, pollination, plant communication, or P. selloum:

Plant tropism –

pollination –

plant communication –

P. selloum
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