The Upside Down World of Orchid Flowers

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Did you know that most orchid flowers you see are actually blooming upside down? That's right, referred to as "resupination," the lower lip of many orchid flowers is actually the top petal and, as the flower develops inside the bud, the whole structure makes a 180° rotation. How and why does this happen?

The lip of an orchid flower usually serves to attract pollinators as well as function as a landing pad for them. The flower of an orchid is an incredibly complex organ with an intriguing evolutionary history. Basically, the lip is the most derived structure on the flower and, in most cases, it is the most important structure in initiating pollination.

 The non-resupinate flowers of the grass pink ( Calopogon tuberosus ) showing the lip on top.

The non-resupinate flowers of the grass pink (Calopogon tuberosus) showing the lip on top.

As an orchid flower bud develops, it begins to exhibit gravitropic tendencies, meaning it responds to the pull of gravity. By removing specific floral organs like the column and pollinia, researchers found that they produce special hormones called auxins that tell the developing bud to begin the process of resupination. The ovary starts to twist, causing the flower to stand on its head.

Not all orchids exhibit resupinate flowers. Grass pinks (Calopogon tuberosus) famously bloom with the lip pointing up as it does in the early stages of bud development. It is an interesting mechanism and serves to demonstrate the stepwise tendencies that the forces of natural selection and evolution can manifest. But why does it occur at all? What is the evolutionary advantage of resupinate flowers?

 Not only are  Dracula  flowers resupinate, many species also face them towards the ground.

Not only are Dracula flowers resupinate, many species also face them towards the ground.

The most likely answer to this biological twist is that, for orchids, resupination places the lip in such a way that facilitates pollination by whatever the flowers are attracting. For many orchids, this means providing an elaborate landing strip in the form of the lip. For the grass pinks, which operate by slamming visiting bees downward onto the column to achieve pollination, placing the lip at the top makes more mechanical sense. When a bee visits the upward pointing lip thinking it will find a pollen-rich meal, the lip bend at the base like a hinge. Anything goes in evolution provided the genes are present for selection to act upon and nowhere is this fact more beautifully illustrated than in orchids.

Further Reading: [1] [2] [3]

Viper's Bugloss

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Throughout much of North America, brown fields, roadsides, and other waste places occasionally take on a wonderful blue hue. Often time the cause of this colorful display is none other than Echium vulgare, or as its commonly referred to, viper's bugloss. Viper’s bugloss is a member of the borage family and was originally native to most of Europe and Asia. However, humans introduced it to North America some time ago. It has since naturalized quite well and is even considered invasive in parts of Washington. No matter your views on this plant, the reproductive ecology of this species is quite interesting.

Viper's bugloss produces its flowers on spikes. Starting off pink and gradually changing to blue as they mature, the flowers ripen their male portions on their first day and ripen their female portions on the second day. This is known as "protandry." Plants that exhibit this lifestyle offer researchers a window into the advantages and disadvantages with regards to the fitness investment of each sex. What they have found in viper's bugloss is that there are clearly distinct strategies for each type of flower.

Male flowers are pollinator limited. They must hedge their bets towards increasing the number of visitors. Bees are the main pollinators of this species and the more bees that visit, the more pollen can be disseminated. Unlike female flowers, which are resource limited, male flowers can produce pollen and nectar quite cheaply. Because of this, male flowers produce significantly more nectar than female flowers to bring in more bees. As the anthers senesce and give way to receptive styles, things begin to change. The plant now has to redirect resources into producing seed. At this point, resources are everything. The plant produces considerably less nectar resources than pollen but the bees can’t know that without visiting.

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The other interesting aspect its reproductive ecology has to do with population size. Bees are notorious for favoring plants that are more numerous on the landscape. This makes a lot of sense. Why spend time looking for uncommon plants when they can go for easier, more numerous targets. This can be very detrimental to the fitness of rare plant species. However, plants like viper's bugloss don't seem to fall victim to this.

By looking at large and small populations, researchers found that pollination success pretty much evens out for viper's bugloss no matter how numerous it is in a given area. Large populations receive many more visits from bees but the bees spend less time on each flower. When viper's bugloss populations are small, flowers receive fewer visits but bees spend more time at each flower. This results is no significant difference in the reproductive fitness of either population.

Considering how efficient this plant is reproductively, it is no wonder it has done so well outside of its native range. Add to this its ability to grow in some of the worst soil conditions, it goes without saying that viper's bugloss is here to stay. If you find this species growing, certainly take time to get up close with the flowers. You will be glad you did.

Photo Credits: [1] [2]

Further Reading: [1] [2] [3]


Rodents as Pollinators

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It may come as a surprise to some that small mammals such as rodents, shrews, and even marsupials have been coopted by plants for pollination services. Far from being occasional evolutionary oddities, many plants have coopted small furry critters for their reproductive needs. Some of the best illustrations of this phenomenon occur in the Protea family (Proteaceae).

  Protea nana

Protea nana

The various members of Proteaceae are probably best known for their bizarre floral displays. Indeed, they are most often encountered outside of their native habitats as outlandish additions to the cut flower industry. Superficial interest in beauty aside, the floral structure of the various protea genera and species is complex to say the least. They are well adapted to ensure cross pollination regardless of what the inflorescence attracts. Most notable is the fact that pollen doesn’t stay on the anthers. Instead, it is deposited on the tip of a highly modified style, which is referred to as the pollen presenter. Usually these structures remain closed until some visiting animal triggers their release.

 The inconspicuous floral display of  Protea cordata .

The inconspicuous floral display of Protea cordata.

Although birds and insects have taken up a majority of the pollination needs of this family, small mammals have entered into the equation on multiple occasions. Pollination by rodents, shrews, and marsupials is collectively referred to as therophilly and it appears to be quite a successful strategy at that. Therophilous pollination has arisen in more than one genera within Proteaceae.

  Leucospermum arenarium  in the field and one of its pollinators,  Gerbillurus paeba,  feeding on flowers. (A) Pollen presenter contact on  G. paeba . (B)  G. paeba  foraging on  L. arenarium   [Source]

Leucospermum arenarium in the field and one of its pollinators, Gerbillurus paeba, feeding on flowers. (A) Pollen presenter contact on G. paeba. (B) G. paeba foraging on L. arenarium [Source]

A therophilous pollination syndrome appears to come complete with a host of unique morphological characters aimed at keeping valuable pollen and nectar away from birds and insects. The inflorescences of therophilous species like Protea nana, P. cordata, and Leucospermum arenarium are usually tucked deep inside the branches of these bushes, often at or near ground level. They are also quite robust and sturdy in nature, which is thought to be an adaptation to avoid damage incurred by the teeth of hungry mammals. The inflorescences of therophilous proteas also tend to have brightly colored or even shiny flowers surrounded by inconspicuous brown involucral bracts.

 (C) Flowering  L. arenarium  with dense, mat-forming inflorescences. (D) Geoflorous inflorescences. (E) Pendulous inflorescences above ground level.  [Source]

(C) Flowering L. arenarium with dense, mat-forming inflorescences. (D) Geoflorous inflorescences. (E) Pendulous inflorescences above ground level. [Source]

Contrasted against bird pollinated proteas, these inflorescences can seem rather drab but that is because small mammals like rodents and shrews are drawn in by another sense - smell. Therophilous proteas tend to produce inflorescences with strong musty or yeasty odors. They also produce copious amounts of sugar-rich, syrupy nectar. Small mammals, after all, need to take in a lot of calories throughout their waking hours and it appears that proteas use that to their advantage.

 A small mouse pollinating  Protea nana

A small mouse pollinating Protea nana

As a rodent or shrew slinks in to take a drink, its head gets completely covered in pollen. In fact, they become so dusted with pollen that, before small, easy to hide trail cameras became affordable, pollen loads in the feces of rodents were the main clue that these plants were attracting something other than birds or insects. What’s more, the flowering period of many of these therophilous proteas occurs in the spring, right around the time when many small mammals go into breeding mode. Its during this time that small mammals need all of the energy they can get.

  Protea humiflora  being pollinated by two different species of rodent in South Africa.

Protea humiflora being pollinated by two different species of rodent in South Africa.

As odd as it may seem, rodent pollination appears to be a successful strategy for a considerable amount of protea species. The proteas aren’t alone either. Other plants appear to have evolved therophilous pollination as well. Nature, after all, works with what it has available and small mammals like rodents make up a considerable portion of regional faunas. With that in mind, it is no wonder that more plants have not converged on a similar strategy. Likely many have, we just need to take the time to sit down and observe.

Photo Credits: [1] [2] [3] [4] [5] [6] [7]

Further Reading: [1] [2] [3] [4] [5]



Cycad Pollinators

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When it comes to insect pollination, flowering plants get all of the attention. However, flowers aren't the only game in town. More and more we are beginning to appreciate the role insects play in the pollination of some gymnosperm lineages. For instance, did you know that many cycad species utilize insects as pollen vectors? The ways in which these charismatic gymnosperms entice insects is absolutely fascinating and well worth understanding in more detail.

Cycads or cycad-like plants were some of the earliest gymnosperm lineages to arise on this planet. They did so long before familiar insects like bees, wasps, and butterflies came onto the scene. It had long been assumed that, like a vast majority of extant gymnosperms, cycads relied on the wind to get pollen from male cones to female cones. Indeed, many species certainly utilize to wind to one degree or another. However, subsequent work on a few cycad genera revealed that wind might not cut it in most cases.

 White-haired cycad ( Encephalartos friderici-guilielm i)

White-haired cycad (Encephalartos friderici-guilielmi)

It took placing living cycads into wind tunnels to obtain the first evidence that something strange might be going on with cycad pollination. The small gaps on the female cones were simply too tight for wind-blown pollen to make it to the ovules. Around the same time, researchers began noting the production of volatile odors and heat in cycad cones, providing further incentives for closer examination.

Subsequent research into cycad pollination has really started to pay off. By excluding insects from the cones, researchers have been able to demonstrate that insects are an essential factor in the pollination of many cycad species. What's more, often these relationships appear to be rather species specific.

  Cycadophila yunnanensis ,  C. nigra , and other beetles on a cone of  Cycas  sp.

Cycadophila yunnanensis, C. nigra, and other beetles on a cone of Cycas sp.

By far, the bulk of cycad pollination services are being performed by beetles. This makes a lot of sense because, like cycads, beetles evolved long before bees or butterflies. Most of these belong to the superfamily Cucujoidea as well as the true weevils (Curculionidae). In some cases, beetles utilize cycad cones as places to mate and lay eggs. For instance, male and female cones of the South African cycad Encephalartos friderici-guilielmi were found to be quite attractive to at least two beetle genera. 

Beetles and their larvae were found on male cones only after they had opened and pollen was available. Researchers were even able to observe adult beetles emerging from pupae within the cones, suggesting that male cones of E. friderici-guilielmi function as brood sites. Adult beetles carrying pollen were seen leaving the male cones and visiting the female cones. The beetles would crawl all over the fuzzy outer surface of the female cones until they became receptive. At that point, the beetles wriggle inside and deposit pollen. Seed set was significantly lower when beetles were excluded.

 Male cone of  Zamia furfuracea  with a mating (lek) assembly of  Rhopalotria mollis  weevils.

Male cone of Zamia furfuracea with a mating (lek) assembly of Rhopalotria mollis weevils.

For the Mexican cycad Zamia furfuracea, weevils also utilize cones as brood sites, however, the female cones go to great lengths to protect themselves from failed reproductive efforts. The adult weevils are attracted to male cones by volatile odors where they pick up pollen. The female cones are thought to also emit similar odors, however, larvae are not able to develop within the female cones. Researchers attribute this to higher levels of toxins found in female cone tissues. This kills off the beetle larvae before they can do too much damage with their feeding. This way, the cycad gets pollinated and potentially harmful herbivores are eliminated. 

Beetles also share the cycad pollination spotlight with another surprising group of insects - thrips. Thrips belong to an ancient order of insects whose origin dates back to the Permian, some 298 million years ago. Because they are plant feeders, thrips are often considered pests. However, for Australian cycads in the genus Macrozamia, they are important pollinators.

  Macrozamia macleayi  female cone.

Macrozamia macleayi female cone.

Thrip pollination was studied in detail in at least two Macrozamia species, M. lucida and M. macleayi. It was noted that the male cones of these species are thermogenic, reaching peak temperatures of around   104 °F (40 °C). They also produce volatile compounds like monoterpenes as well as lots of CO2 and water vapor during this time. This spike in male cone activity also coincides with a mass exodus of thrips living within the cones.

 Thrips ( Cycadothrips chadwicki ) leaving a thermogenic pollen cone of  Macrozamia lucida.

Thrips (Cycadothrips chadwicki) leaving a thermogenic pollen cone of Macrozamia lucida.

Thrips apparently enjoy cool, dry, and dark places to feed and breed. That is why they love male Macrozamia cones. However, if the thrips were to remain in the male cones only, pollination wouldn't occur. This is where all of that male cone metabolic activity comes in handy. Researchers found that the combination of rising heat and humidity, and the production of monoterpenes aggravated thrips living within the male cones, causing them to leave the cones in search of another home.

Inevitably many of these pollen-covered thrips find themselves on female Macrozamia cones. They crawl inside and find things much more to their liking. It turns out that female Macrozamia cones do not produce heat or volatile compounds. In this way, Macrozamia are insuring pollen transfer between male and female plants.

 Thrips up close.

Thrips up close.

Pollination in cycads is a fascinating subject. It is a reminder that flowering plants aren't the only game in town and that insects have been providing such services for eons. Additionally, with cycads facing extinction threats on a global scale, understanding pollination is vital to preserving them into the future. Without reproduction, species will inevitably fail. Many cycads have yet to have their pollinators identified. Some cycad pollinators may even be extinct. Without boots on the ground, we may never know the full story. In truth, we have only begun to scratch the surface of cycads and their pollinators.

Photo Credits: [1] [2] [3] [4] [5] [6] [7]

Further Reading: [1] [2] [3] [4] [5] [6]

Meet the Crypts

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If you have ever spent time in an aquarium store, you have undoubtedly come across a Cryptocoryne or two. Indeed, these plants are most famous for their indispensable role in aquascaping freshwater aquaria. As organisms, however, crypts receive considerably less attention. Nonetheless, a handful of dedicated botanists have devoted time and effort to understanding this wonderful genus of tropical Aroids. What follows is a brief introduction to the world of Cryptocoryne plants. 

Cryptocoryne is a genus that currently consists of around 60 - 65 species, all of which are native to tropical regions of Asia and New Guinea. Every few years it seems at least one or two new species are added to this list and without a doubt, more species await discovery. All crypts are considered aquatic to one degree or another. Ecologically speaking, however, species fall into four broad categories based on the types of habitats they prefer.

  Cryptocoryne cognata in situ .

Cryptocoryne cognata in situ.

The most familiar crypts grow along the banks of slow-moving rivers and streams and find themselves submerged for a large portion of their life. Others grow in seasonally flooded habitats and experience a pronounced dry season. These species usually go dormant until flood waters return. Still others can be found growing in swampy forested habitats, often in acidic peat swamps. Finally, a few crypts have adapted to living in tidal zones in both fresh and brackish waters.

Like all aquatic plants, crypts face a lot of challenges living in water. One of the biggest challenges is reproduction. Despite their aquatic nature, crypts will not flower successfully underwater. If growing submerged, most crypt species reproduce vegetatively via a creeping rhizome. As such, crypts often form large, clonal colonies in both the wild and in aquaria, a fact that has made a few crypts aggressive invaders in places like Florida.

  Cryptocoryne wendtii  is one of the most common species in the aquarium trade. Its textured leaves are thought to have a higher surface area, allowing this plant to thrive in shaded aquatic habitats.

Cryptocoryne wendtii is one of the most common species in the aquarium trade. Its textured leaves are thought to have a higher surface area, allowing this plant to thrive in shaded aquatic habitats.

Given proper hydrologic cycles, however, crypts will flower and when they do, it is truly a sight to behold. As is typical of aroids, crypts produce an inflorescence comprised of a spadix with whirls of male and female flowers covered by a decorative sheath called a spathe. This spathe is the key to successful flowering among the various crypt species.

 Species like  C. becketti  have become invasive in places like Florida, no doubt thanks to aquarium hobbyists.

Species like C. becketti have become invasive in places like Florida, no doubt thanks to aquarium hobbyists.

If the spathe were to open underwater, the inflorescence would quickly rot. Instead, most crypts seem to have an uncanny ability to sense water levels. At early stages of development, the spathe completely encloses the developing spadix in a water tight package. The tubular spathe continues to grow upward until the top has breached the surface. Consequently, the overall length of a crypt inflorescence is highly variable depending on the water level of its habitat. Crypts living in tidal zones take this a step further. Somehow they are able to time their flowering events to the ebb and flow of the tides, only producing flowers during periods of the month when tides are at their lowest.

  Cryptocoryne ligua

Cryptocoryne ligua

With the tip of the inflorescence safely above water, the spathe will finally open revealing their surprisingly complex anatomy and coloration. It is a shame that most crypt growers never get to see such floral splendor in person. The spathe of many crypt species emit a faint but unpleasant odor. Additionally, some species adorn the spathe with fringes that, coupled with stark coloration, is thought to improve the chances of pollinator visitation.

Pollinators are poorly studied among crypts, however, it is thought that small flies take up the bulk of the work. Lured in by the promise of a rotting meal on which they can feed and lay their eggs, the flies become trapped inside the long tube of the spathe. Like the pitfall traps of a pitcher plant, the inner walls of the spathe are coated in a waxy substance that keeps the insects from crawling out before they do their job.

In general, the female flowers mature first. If the insect inside has visited a crypt of the same species the day before, it is likely carrying pollen and thus deposits said pollen onto the stigmas of the current crypt. After the female flowers have had a chance at being fertilized, the male flowers then mature. The insects inside are then dusted with new pollen, the walls of the spathe lose their slippery properties, and the insects are released in hopes of repeated the process again.

 The fruit of a  Cryptocoryne  is called a syncarp.

The fruit of a Cryptocoryne is called a syncarp.

To the best of my knowledge, most crypts are not self-compatible. Instead, plants must receive pollen from unrelated individuals to set seed. Because large crypt colonies are often made up of clones of a single mother plant, sexual reproduction can be rather infrequent among the various species. Nonetheless sexual reproduction does occur and the seeds are produced in a different way than most other aroids. Instead of berries, crypts produce their seeds in a aggregated collection of fruits called a syncarp. When ripe, the syncarp opens like a little star and the seeds float away on the current.

One species, Cryptocoryne ciliata, takes seed production to a whole different level by producing viviparous seeds. Before the syncarp even opens, the seeds actually germinate on the mother plant. In this way, tiny seedlings complete with roots and leaves are released instead of seeds. Seedlings have a much greater surface area than seeds and readily get stuck in mud as well as other aquatic vegetation. In this way, C. ciliata offspring get a jump start on the establishment process. It is no wonder then that C. ciliata has one of the widest distributions of any of the crypt species.

  Cryptocoryne ciliata

Cryptocoryne ciliata

Despite plenty of overlap among the ranges of various crypt species, the genus displays an amazing array of variation. Some have likened crypts to Araceae's version of Darwin's finches in that the unique ecology of each species appears to have created barriers to species introgression. Though hybrids do occur, each crypt seems to maintain its own niche via a unique habitat requirement, differing flower phenology, or a specific set of pollinators. It would appear that much can be learned about the mechanics of speciation by studying the various Cryptocoryne and their habits.

Unfortunately, the limited geographic distribution and specific habitat requirements of crypt species is cause for concern. Many are growing more and more rare as human settlements expand and destroy valuable crypt habitat. As popular as some crypts may be in cultivation, many others have proven too idiosyncratic to grow on a commercial level. More work is certainly needed to properly assess populations and bring plants into cultivation as a form of ex situ conservation.

  Cryptocoryne cordata  Var. Siamensis 'Rosanervig' is a contoversial variety names recognized by the stark patterns of venation on its leaves.

Cryptocoryne cordata Var. Siamensis 'Rosanervig' is a contoversial variety names recognized by the stark patterns of venation on its leaves.

Proper study is further complicated by the fact that many crypt species are highly plastic. They have to be in order to survive the rigors of their aquatic environment. True species identification can really only be assessed when flowers are present and some populations seem to prefer vegetative over sexual reproduction a majority of the time. A multitude of subspecies exist, though the degree to which they should be formally recognized is up for debate.

I think it is safe to say that Cryptocoryne is a genus worth far more attention than it currently receives. They are without a doubt important components of the ecology of their native habitats and humans would do well to understand them a bit better. With a bit more attention from botanical gardens and other conservation organizations, perhaps the future for many crypts does not have to be so bleak.

Photo Credits: [1] [2] [3] [4] [5]

Further Reading: [1] [2] [3] [4] [5]

 

Toxic Nectar

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I was introduced to the concept of toxic nectar thanks to a species of shrub quite familiar to anyone who has spent time in the Appalachian Mountains. Locals will tell you to never place honeybee hives near a patch of rosebay (Rhododendron maximum) for fear of so-called "mad honey." Needless to say, the concept intrigued me.

A quick internet search revealed that this is not a new phenomenon either. Humans have known about toxic nectar for thousands of years. In fact, honey made from feeding bees on species like Rhododendron luteum and R. ponticum has been used more than once during times of war. Hives containing toxic honey would be placed along known routs of Roman soldiers and, after consuming the seemingly innocuous treat, the soldiers would collapse into a stupor only to be slaughtered by armies lying in wait.

  Rhododendron luteum

Rhododendron luteum

The presence of toxic nectar seems quite confusing. The primary function of nectar is to serve as a reward for pollinators after all. Why on Earth would a plant pump potentially harmful substances into its flowers?

It is worth mentioning at this point that the Rhododendrons aren't alone. A multitude of plant species produce toxic nectar. The chemicals that make them toxic, though poorly understood, vary almost as much as the plants that make them. Although there have been repeated investigations into this phenomenon, the exact reason(s) remain elusive to this day. Still, research has drummed up some interesting data and many great hypotheses aimed at explaining the patterns.

 Catalpa nectar has been shown to deter some ants and butterflies but not large bees.

Catalpa nectar has been shown to deter some ants and butterflies but not large bees.

The earliest investigations into toxic nectar gave birth to the pollinator fidelity hypothesis. Researchers realized that meany bees appear to be less sensitive to alkaloids in nectar than are some Lepidopterans. This led to speculation that perhaps some plants pump toxic compounds into their nectar to deter inefficient pollinators, leading to more specialization among pollinating insects that can handle the toxins.

Another hypothesis is the nectar robber hypothesis. This hypothesis is quite similar to the pollinator fidelity hypothesis except that it extends to all organisms that could potentially rob nectar from a flower without providing any pollination services. As such, it is a matter of plant defense.

 The nectar of  Cyrilla racemiflora  is thought to be toxic to some bees.

The nectar of Cyrilla racemiflora is thought to be toxic to some bees.

Others feel that toxic nectar may be less about pollinators or nectar robbers and more about microbial activity. Sugary nectar can be a breeding ground for microbes and it is possible that plants pump toxic compounds into their nectar to keep it "fresh." If this is the case, the antimicrobial benefits could outweigh the cost to pollinators that may be harmed or even deterred by the toxic compounds.

Finally, it could be that toxic nectar may have no benefit to the plant whatsoever. Perhaps toxic nectar is simply the result of selection for defense compounds elsewhere in the plant and therefore is expressed in the nectar as a result of pleiotropy. If this is the case then toxic nectar might not be under as strong selection pressures as is overall defense against herbivores. If so, the plants may not be able to control which compounds eventually end up in their nectar. Provided defense against herbivores outweighs any costs imposed by toxic nectar then plants may not have the ability to evolve away from such traits.

 Where Spathodea campanulata is invasive, its nectar causes increased mortality in native bee hives.

Where Spathodea campanulata is invasive, its nectar causes increased mortality in native bee hives.

So, where does the science land us with these hypotheses? Do the data support any of these theories? This is where things get cloudy. Despite plenty of interest, evidence in support of the various hypotheses is scant. Some experiments have shown that indeed, when given a choice, some bees prefer non-toxic to toxic nectar. Also, toxic nectar appears to dissuade some ants from visiting flowers, however, just as many experiments have demonstrated no discernible effect on bees or ants. What's more, at least one investigation found that the amount of toxic compounds within the nectar of certain species varies significantly from population to population. What this means for pollination is anyone's' guess.

It is worth noting that most of the pollination-related hypotheses about toxic nectar have been tested using honeybees. Because they are generalist pollinators, there could be something to be said about toxic nectar deterring generalist pollinators in favor of specialist pollinators. Still, these experiments have largely been done in regions where honeybees are not native and therefore do not represent natural conditions.

Simply put, it is still too early to say whether toxic nectar is adaptive or not. It could very well be that it does not impose enough of a negative effect on plant fitness to evolve away from. More work is certainly needed. So, if you are someone looking for an excellent thesis project, here is a great opportunity. In the mean time, do yourself a favor and don't eat any mad honey.

Photo Credits: [1] [2] [3] [4]

Further Reading: [1] [2] [3] [4] [5] [6]

 

 

The Trumpet Creeper

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With its impressive bulk and those stunning tubular red flowers, one would be excused for thinking that the trumpet creeper (Campsis radicans) was a tropical vine. Indeed, the family to which it belongs, Bignoniaceae, is largely tropical in its distribution. There are a handful of temperate representatives, however, and the trumpet creeper is one of the most popular. Its beauty aside, this plant is absolutely fascinating.

As many of you probably know, the trumpet creeper can reach massive proportions. In the garden, this can often result in collapsed structures as its weight and speed of growth is something few adequately prepare for. In the wild, I most often see this vine in somewhat disturbed forests, usually near a floodplain. As such, it is supremely adapted to take a hit and keep on growing year after year.

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One of the many reasons this plant performs so well both where it is native and where it is not is that it recruits body guards. This is easy to witness in a garden setting as the branches and especially the flowers are frequently crawling with ants. Trumpet creepers trade food for protection via specialized organs called extrafloral nectaries. These structures secrete sugary nectar that is readily sucked up by tenacious ants. When a worker ant finds a vine, more workers are soon to follow. 

Amazingly for a temperate plant, trumpet creepers produce more extrafloral nectaries of all four categories - petiole, calyx, corolla, and fruit. What this means is that all of the important organs are covered in insects that viciously attack anything that might threaten this sugary food supply. Hassle one of these vines at your own peril. With its photosynthetic and reproductive structures protected, trumpet creepers make a nice living once established.

Reproduction is another fascinating aspect of trumpet creeper biology. A closer inspection of the floral anatomy will reveal a bilobed stigma. Amazingly, this stigma has the ability to open and close as potential pollinators visit the flowers. Stigmatic movement in the trumpet creeper has attracted a bit of attention from researchers over the years. What is its function?

Evidence suggests that the opening and closing of the lobed stigma is way of increasing the chances of pollination. Touch alone is not enough to trigger the movement. However, when researchers dusted pollen onto the stigma, then it began to close. What's more, this action happens within 15 to 60 seconds. Amazingly, there appears to be a threshold to whether the stigma stays closed or reopens after 3 hours or so.

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It turns out, the threshold seems to depend on the amount of pollen being deposited. Only after 350 grains found their way onto the stigma did it close permanently. Experts feel that this a means by which the plant ensured ample seed set. If too few pollen grains end up on the stigma, the plant risks not having all of its ovules fertilized. By permanently closing after enough pollen grains are present, the plant can ensure that the pollen grains can germinate and fertilize the ovules without being brushed off.

It is interesting to note that the flowers frequently remain on the plant after they have been fertilized. This likely serves to maintain a largely floral display that continues to attract pollinators until most of the flowers have been pollinated. Speaking of pollinators, observations have revealed that the trumpet creeper is pollinated primarily by ruby-throated hummingbirds. Although insects like bumblebees frequently visit these blooms, bringing pollen with them in the process, hummingbirds, on average, bring and deposit 10 times as much pollen as any other visitor. And, considering the threshold on pollen mentioned above, trumpet creeper appears to have evolved a pollination syndrome with these lovely little birds.

Photo Credits: [1] [2] [3] [4]

Further Reading: [1] [2] [3] [4]

How Aroids Turn Up the Heat

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A subset of plants have evolved the ability to produce heat, a fact that may come as a surprise to many reading this. The undisputed champions of botanical thermogenesis are the aroids (Araceae). Exactly why they do so is still the subject of scientific debate but the means by which heat is produced is absolutely fascinating.

The heat producing organ of an aroid is called the spadix. Technically speaking, a spadix is a spike of minute flowers closely arranged around a fleshy axis. All aroid inflorescences have one and they come in a wide variety of shapes, colors, and textures. To produce heat, the spadix is hooked up to a massive underground energy reserve largely in the form of carbohydrates or sugars. The process of turning these sugars into heat is rather complex and surprisingly animal-like.

 Cross section of a typical aroid inflorescence with half of the protective spathe removed. The spadix is situated in the middle with a rings of protective hairs (top), male flowers (middle), and female flowers (bottom).

Cross section of a typical aroid inflorescence with half of the protective spathe removed. The spadix is situated in the middle with a rings of protective hairs (top), male flowers (middle), and female flowers (bottom).

It all starts with a compound we are rather familiar with - salicylic acid - as it is the main ingredient in Aspirin. In aroids, however, salicylic acid acts as a hormone whose job it is to initiate both the heating process as well as the production of floral scents. It signals the mitochondria packed inside a ring of sterile flowers located at the base of the spadix to change their metabolic pathway.

In lieu of their normal metabolic pathway, which ends in the production of ATP, the mitochondria switch over to a pathway called the "Alternative Oxidase Metabolic Pathway." When this happens, the mitochondria start burning sugars using oxygen as a fuel source. This form of respiration produces heat.

 Thermal imaging of the inflorescence of  Arum maculatum .

Thermal imaging of the inflorescence of Arum maculatum.

As you can imagine, this can be a costly process for plants to undergo. A lot of energy is consumed as the inflorescence heats up. Nonetheless, some aroids can maintain this costly level of respiration intermittently for weeks on end. Take the charismatic skunk cabbage (Symplocarpus foetidus) for example. Its spadix can reach temperatures of upwards of 45 °F (7 °C) on and and off for as long as two weeks. Even more incredible, the plant is able to do this despite freezing ambient temperatures, literally melting its way through layers of snow.

For some aroids, however, carbohydrates just don't cut it. Species like the Brazilian Philodendron bipinnatifidum produce a staggering amount of floral heat and to do so requires a different fuel source - fat. Fats are not a common component of plant metabolisms. Plants simply have less energy requirements than most animals. Still, this wonderful aroid has converged on a fat-burning metabolic pathway that puts many animals to shame. 

 The inflorescence of  Philodendron bipinnatifidum  can reach temps as high as 115 °F (46 °C)

The inflorescence of Philodendron bipinnatifidum can reach temps as high as 115 °F (46 °C)

P. bipinnatifidum stores lots of fat in sterile male flowers that are situated between the fertile male and female flowers near the base of the spadix. As soon as the protective spathe opens, the spadix bursts into metabolic action. As the sun starts to set and P. bipinnatifidum's scarab beetle pollinators begin to wake up, heat production starts to hit a crescendo. For about 20 to 40 minutes, the inflorescence of P. bipinnatifidum reaches temperatures as high as 95 °F (35 °C) with one record breaker maxing out at 115 °F (46 °C)! Amazingly, this process is repeated again the following night.

It goes without saying that burning fat at a rate fast enough to reach such temperatures requires a lot of oxygen. Amazingly, for the two nights it is in bloom, the P. bipinnatifidum inflorescence consumes oxygen at a rate comparable to that of a flying hummingbird, which are some of the most metabolically active animals on Earth.

 The world's largest inflorescence belongs to the titan arum ( Amorphophallus titanum ) and it too produces heat.

The world's largest inflorescence belongs to the titan arum (Amorphophallus titanum) and it too produces heat.

Again, why these plants go through the effort of heating their reproductive structures is still a bit of a mystery. For most, heat likely plays a role in helping to volatilize floral scents. Anyone that has spent time around blooming aroids knows that this plant family produces a wide range of odors from sweet and spicy to downright offensive. By warming these compounds, the plant may be helping to lure in pollinators from a greater distance away. It is also thought that the heat may be an attractant in and of itself. This is especially true for temperate species like the aforementioned skunk cabbage, which frequently bloom during colder months of the year. Likely both play a role to one degree or another throughout the aroid family.

What we can say is that the process of plant thermogenesis is absolutely fascinating and well worth deeper investigation. We still have much to learn about this charismatic group of plants.

LEARN MORE ABOUT AROID POLLINATION HERE

Photo Credits: [1] [2] [3] [4] [5]

Further Reading: [1] [2] [3] [4] [5] [6] [7] [8]

 

Pollen Competition

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The animal kingdom is rife with sexual conflict. We are all aware of what is going on when two stag deer lock antlers or when a group of male sage grouse flaunt themselves on leks as females look on. But what about plants? Is there sexual conflict among plant species? Whether pollen ends up on a stigma via wind or animal, is there any way for a plant to "choose" who gets to fertilize the ovule?

It turns out, yes, there is. Sexual competition is part of the pollination process. In fact, some of the most familiar floral morphologies may have evolved as a way of weeding out weak paternal lines. To understand this process better, though, we must first quickly review exactly what goes on during pollination.

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Pollen is a male gamete. Each grain is haploid and contains only a single copy of a plants' chromosomes. When a pollen grain lands on a stigma, the grain germinates like a tiny seed, sending down a root-like growth called a pollen tube. This tube grows down into the ovary until it finds an unfertilized ovule. At this point, sperm travels down the pollen tube where it can unite with the ovule, thus forming a seed.

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Its the formation of this pollen tube that introduces the idea of competition among pollen grains. Again, whether by wind or animal, the pollen arriving to a new plant generally doesn't come from a single individual. Pollen from many potential fathers can arrive all at once. As such, the race to fertilize the ovules can be quite intense, and this is where competition begins.

Remember, pollen only contains a single set of chromosomes from the parent plant, thus all alleles, both functioning and deleterious, are represented. During the growth of the pollen tube, upwards of 60% of the pollen genome is actively transcribed. Any pollen containing lots of deleterious alleles is going to have a much harder time competing with pollen grains that have fewer deleterious alleles. Their tubes have a harder time making it to the ovules in time to fertilize them.

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It is thought that the length of the style (the stem connecting the stigma to the ovaries) may also provide a sort of "proving ground" for pollen too. For instance, picture the flowers of a lily or a mallow. Those long, slender styles may actually be acting like a race track. Only the pollen with the best selection of genetic material will be able to grow their pollen tubes fast enough to reach the ovules, leaving the weaker competition in the dust. In this way, plants may actually be sorting out stronger paternal lines, which makes sense for sessile organisms that can't see.

As with everything in nature, there is far more nuance to this than what I have outlined above. Much work is being done to test some of the earlier assumptions and data surrounding this concept of pollen competition. It certainly happens but the degree to which any given species utilizes such methods is up for debate. Still, it paints a much more interesting picture of mate selection in plants. Static, plants are not!

Photo Credits: [1] [2] [3] [4] [5]

Further Reading: [1] [2] [3] [4] [5] [6] [7]

 

The Intriguing Pollination of a Central American Anthurium

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As an avid gardener of both indoors and out, there are few better experiences than getting to see familiar plants growing in the wild for the first time. That experience is made all the better when you find out new and interesting facts about their ecology. On a recent trip to Costa Rica, I was introduced to a wide variety of Anthurium species. I marveled at how amazing these plants look in situ and was taken aback to learn that many produce flowers with intoxicating aromas.

I was also extremely fortunate to be in the presence of some aroid experts during this trip and their knowledge fueled my interest in getting up close and personal with what little time I had with these plants. They were able to ID the plants and introduce me to their biology. One species in particular has been the subject of interest in an ongoing pollination study that has proven to be unique.

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The plant in question is known scientifically as Anthurium acutifolium and it is rather charming once you get to know it. It is a terrestrial plant with relatively large leaves for its overall size. Its range includes portions of lowland Costa Rica and Panama. Its flowers are typical of what one would expect out of this family. They are fused into a type of inflorescence known as a spadix and can range in color from white to green and occasionally red. If you are lucky to visit the spadix between roughly 8:00 AM and 12:30 PM, you may notice a rich scent that, to me, is impossible to describe in words.

It's this scent that sets the stage for pollination in this species. During some down time, University of Vienna grad student Florian Etl discovered that the spadix of A. acutifolium was getting a lot of attention from a particular species of small bee. Closer inspection revealed that they were all males of a species of oil-collecting bee known as Paratetrapedia chocoensis. Now, the females of these oil collecting bees are well known in the pollination literature. They visit flowers that secrete special oils that the females then use to build nests and feed their young. This is why the attention from male bees was so intriguing.

 A: A male  P. chocoensis  bee approaching a scented spadix of an inflorescence of  A. acutifolium . B: The abdominal mopping behavior of male  P. chocoensis  oil bees on a spadix. C: Ventral side of the abdomen of a male  P.chocoensis  covered with pollen. D: A male  P. chocoensis  bee on a spadix of an inflorescence of  A. acutifolium , touching the pollen shedding anthers. E: Pubescent region pressed on the surface of  A. acutifolium  during the mopping behavior. F: A scented inflorescence of  A. acutifolium  with three male  P. chocoensis  individuals. G: Image of the abdomen of a male  P.chocensis  in lateral view showing the conspicuous pubescent region. ( SOURCE )

A: A male P. chocoensis bee approaching a scented spadix of an inflorescence of A. acutifolium. B: The abdominal mopping behavior of male P. chocoensis oil bees on a spadix. C: Ventral side of the abdomen of a male P.chocoensis covered with pollen. D: A male P. chocoensis bee on a spadix of an inflorescence of A. acutifolium, touching the pollen shedding anthers. E: Pubescent region pressed on the surface of A. acutifolium during the mopping behavior. F: A scented inflorescence of A. acutifolium with three male P. chocoensis individuals. G: Image of the abdomen of a male P.chocensis in lateral view showing the conspicuous pubescent region. (SOURCE)

Males would land on the spadix and begin rubbing the bottom of their abdomen along its surface. In doing so, they inevitably picked up and deposited pollen. To date, such behavior was unknown among male oil bees. What exactly were these male bees up to?

As it turns out, the males were collecting fragrances. Close inspection of their morphology revealed that each male has a small patch of dense hairs underneath their abdomen. The males are definitely not after fatty oils or nectar as A. acutifolium does not secrete either of these substances. Instead, it would appear that the male oil bees are there to collect scent, which is mopped up by that dense patch of hairs. Even more remarkable is the fact that in order to properly collect these fragrance compounds, the bees are likely using solvents that they have collected from other flowering plant species around the forest.

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What they are doing with these scent compounds remains a mystery but some potential clues lie in another scent/pollination system. Male orchid bees perform similar scent-collecting activities in order to procure unique scent bouquets. Though the exact function of their scent collecting is not known either, we do know that these scents are used in the process of finding and procuring mates. It is likely that these male oil bees are using them in a similar way.

Taken together, these data suggest that a very specific pollination syndrome involving A. acutifolium and male oil bees has evolved in Central American forests. No other insects were observed visiting the flowers of A. acutifolium and the scents only ever attracted males of these specific oil bees during the hours in which the spadix was actively producing the compounds. This is a remarkable pollination syndrome and one that encourages us to start looking elsewhere in the forest. This, my friends, is why there is no substitute for simply taking the time to observe nature. We must take the time to get outside and poke around because we stand to miss out on so much of what makes our world tick and without such knowledge, we risk losing so much. 

Photo Credits: Florian Etl [1]

Further Reading: [1]

Daffodil Insights

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Daffodils seem to be everywhere. Their horticultural popularity means that, for many of us, these plants are among the first flowers we see each spring. Daffodils are so commonplace that it's as if they evolved to live in our gardens and nowhere else. Indeed, daffodils have had a long, long history with human civilization, so much so that it is hard to say when our species first started to cohabitate. Our familiarity with these plants belies an intriguing natural history. What follows is a brief overview of the world of daffodils. 

If you are like me, then you may have gone through most of your life not noticing much difference between garden variety daffodils. Though many of us will be familiar with only a handful of daffodil species and cultivars, these introductions barely scratch the surface. One may be surprised to learn that as of 2008, more than 28,000 daffodil varieties have been named and that number continues to grow each and every year. Even outside of the garden, there is some serious debate over the number of daffodil species, much of this having to do with what constitutes a species in this group.

  Narcissus poeticus

Narcissus poeticus

As I write this, all daffodils fall under the genus Narcissus. Estimates as to the number of species within Narcissus range from as few as 50 to as many as 80. The genus itself sits within the family Amaryllidaceae and is believed to have originated somewhere between the late Oligocene and early Miocene, some 18 to 30 million years ago. Despite its current global distribution, Narcissus are largely Mediterranean plants, with peak diversity occurring on the Iberian Peninsula. However, thanks to the aforementioned long and complicated history in cultivation, it has become quite difficult to understand the full range of diversity in form and habitat of many species. To understand this, we first need to understand a bit about their reproductive habits.

Much of the evolution of Narcissus seems to center around floral morphology and geographic isolation. More specifically, the length of the floral tube or "corona" and the position of the sexual organs within, dictates just who can effectively pollinate these plants. The corona itself is not made up of petals or sepals but instead, its tube-like appearance is due to a fusion of the stamens into the famous trumpet-like tube we know and love.

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Variation in corona shape and size has led to the evolution of three major pollination strategies within this genus. The first form is the daffodil form, whose stigma is situated at the mouth of the corolla, well beyond the 6 anthers. This form is largely pollinated by larger bees. The second form is the paperwhite form, whose stigma is situated more closely to or completely below the anthers at the mouth of the corona. This form is largely pollinated by various Lepidoptera as well as long tongued bees and flies. The third form is the triandrus form, which exhibits three distinct variations on stigma and anther length, all of which are situated deep within the long, narrow corona. The pendant presentation of the flowers in this group is thought to restrict various butterflies and moths from entering the flower in favor of bees.

  Narcissus tazetta

Narcissus tazetta

The variations on these themes has led to much reproductive isolation among various Narcissus populations. Plants that enable one type of pollinator usually do so at the exclusion of others. Reproductive isolation plus geographic isolation brought on by differences in soil types, habitat types, and altitudinal preferences is thought to have led to a rapid radiation of these plants across the Mediterranean. All of this has gotten extremely complicated ever since humans first took a fancy to these bulbs.

  Narcissus cyclamineus

Narcissus cyclamineus

Reproductive isolation is not perfect in these plants and natural hybrid zones do exist where the ranges of two species overlap. However, hybridization is made much easier with the helping hand of humans. Whether via landscape disturbance or direct intervention, human activity has caused an uptick in Narcissus hybridization. For centuries, we have been mixing these plants and moving them around with little to no record as to where they originated. What's more, populations frequently thought of as native are actually nothing more than naturalized individuals from ancient, long-forgotten introductions. For instance, Narcissus populations in places like China, Japan, and even Great Britain originated in this manner.

All of this mixing, matching, and hybridizing lends to some serious difficulty in delineating species boundaries. It would totally be within the bounds of reason to ask if some of the what we think of as species represent true species or simply geographic varieties on the path to further speciation. This, however, is largely speculative and will require much deeper dives into Narcissus phylogenetics.

  Narcissus triandrus

Narcissus triandrus

Despite all of the confusion surrounding accurate Narcissus taxonomy, there are in fact plenty of true species worth getting to know. These range in form and habit far more than one would expect from horticulture. There are large Narcissus, small Narcissus, there are Narcissus with yellow flowers and Narcissus with white flowers, some with upright flowers and some with pendant flowers. There are even a handful of fall blooming Narcissus. The variety of this genus is staggering if you are not prepared for it.

  Narcissus viridiflorus  - a green, fall-blooming daffodil

Narcissus viridiflorus - a green, fall-blooming daffodil

After pollination, the various Narcissus employ a seed dispersal strategy that doesn't get talked about enough in reference to this group. Attached to each hard, black seed are fatty structures known as eliasomes. Eliasomes attract ants. Like many spring flowering plant species around the globe, Narcissus utilize ants as seed dispersers. Ants pick up the seeds and bring them back to their nests. They go about removing the eliasomes and then discard the seed. The seed, safely tucked away in a nutrient-rich ant midden, has a much higher chance of germination and survival than if things were left up to simple chance. It remains to be seen whether or not Narcissus obtain similar seed dispersal benefits from ants outside of their native range. Certainly Narcissus populations persist and naturalize readily, however, I am not aware if ants have any part in the matter.

 The endangered  Narcissus alcaracensis .

The endangered Narcissus alcaracensis.

Despite their popularity in the garden, many Narcissus are having a hard go of it in the wild. Habitat destruction, climate change, and rampant collecting of wild bulbs are having serious impacts on Narcissus numbers. The IUCN considered at least 5 species to be endangered and a handful of some of the smaller species already thought to be extinct in the wild. In response to some of these issues, protected areas have been established that encompass at least some of the healthy populations that remain for some of these species.

If you are anything like me, you have ignored Narcissus for far too long. Sure, they aren't native to the continent on which I live, and sure, they are one of the most commonly used plants in a garden setting, but every species has a story to tell. I hope that, armed with this new knowledge, you at least take a second look at the Narcissus popping up around your neighborhood. More importantly, I hope this introduction makes you appreciate their wild origins and the fact that we still have much to learn about these plants. I have barely scratched the surface of this genus and there is more more information out there worth perusing. Finally, I hope we can do better for the wild progenitors of our favorite garden plants. They need all the help they can get and unless we start speaking up and working to preserve wild spaces, all that will remain are what we have in our gardens and that is not a future I want to be a part of.

Photo Credits: [1] [2] [3] [4] [5] [6] [7]

Further Reading: [1] [2] [3] [4] [5] [6] [7] [8] [9]

 

Do Yeasts Aid Pollination For the Stinking Hellebore?

Whether they are growing in their native habitat or in some far away garden, Hellebores are some of the earliest plants to bloom in the spring. Hellebore flowers can often be seen blooming long before the snow has melted away. All early blooming plant species are faced with the challenge of attracting pollinators. Though the competition for insect attention is minimal among these early bloomers, only the hardiest insects are out and about on cold, dreary days. It stands to reason then that anything that can entice a potential pollinator would be of great benefit for a plant.

That is why the presence of yeast in the nectar of at least one species of Hellebore has attracted the attention of scientists. The species in question is known scientifically as Helleborus foetidus. The lack of appeal in its binomial is nothing compared to its various common names. One can often find H. foetidus for sale under names like the "stinking hellebore" or worse, "dungwort." All of these have to do with the unpleasant aroma given off by its flowers and bruised foliage. Surprisingly, that is not the topic of this post.

What is more intriguing about the flowers of H. foetidus is that the nectar produced by its smelly green flowers harbors dense colonies of yeast. Yeasts are everywhere on this planet and despite their economic importance, little is known about how they function in nature. For instance, what the heck are these yeast colonies doing in the nectar of this odd Hellebore?

To test this, two researchers from the Spanish National Research Council manipulated yeast colonies within the flowers to see what might be happening. It turns out, yeast in the nectar of H. foetidus actually warms the flowers. As the yeast feed on the sugars within the nectar, their metabolic activity can raise the temperature of the flowers upwards of 2 °C above the ambient. To date, the only other ways in which floral heating has been achieved is either via specific metabolic processes within the floral tissues or by direct heating from the sun. 

In heating the flowers, these yeast colonies may be having serious impacts on the reproductive success of H. foetidus. For starters, these plants are most at home under the forest canopies of central and western Europe. What's more, many populations find themselves growing in the dense shade of evergreens. This completely rules out the ability to utilize solar energy to heat blooms. Additionally, floral heat can mean more visits by potential pollinators. Experiments have shown that bees preferentially visit flowers that are slightly warmer than ambient temperatures. Even the flowers themselves can benefit from that heat. Warmer flowers have higher pollination rates and better seed set.

  Bombus terrestris  was one of the most common floral visitors of  Helleborus foetidus.

Bombus terrestris was one of the most common floral visitors of Helleborus foetidus.

Yeast colonies also have their downsides. The heat generated by the yeast comes from the digestion of sugars. Indeed, nectar housing yeast colonies had drastically reduced sugar loads than nectar without yeast. This has the potential to offset many of the benefits of floral warming in large part because bees are good at discriminating. Bees are visiting these blooms as a food source and by diminishing the sugar loads within the nectar, the yeast may be turning bees off to this potential source. The question then becomes, do bees prefer heat over sugar-rich food? The authors think there might be a trade-off, with bees preferring heated flowers on colder days and sugar-rich flowers on warmer days.

Though the authors found evidence for heating, they did not test for pollinator preference. All we know at this point is that yeast in the nectar significantly warms H. foetidus flowers. Until we know whether bees are making a decision based on yeast colonies, we cannot say whether this is a case of a mutualism or form of parasitism. Such questions will be the subject of future research. Nonetheless, this is a wonderful example of why we need to pay way more attention to the function of yeasts in nature.

Photo Credits: [1] [2] [3]

Further Reading: [1] [2]

From Herbivore to Pollinator Thanks to a Parasitoid

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In the Atlantic forests of Brazil resides a small orchid known scientifically as Dichaea cogniauxiana. Like most plant species, this orchid experiences plenty of pressure from herbivores. It faces rather intense pressures from two species of weevil in the genus Montella. These weevils are new to science and have yet been given full species status. What's more, they don't appear to eat the leaves of D. cogniauxiana. Instead, female weevils lay eggs in the developing fruits and the larvae hatch out and consume the seeds within. In other words, they treat the fruits like a nursery chamber.

This is where this relationship gets interesting. You see, the weevils themselves appear to take matters into their own hands. Instead of waiting to find already pollinated orchids, an event that can be exceedingly rare in the dense Amazonian forests, these weevils go about pollinating the orchids themselves. Females have been observed picking up orchid pollinia and depositing the pollen onto the stigmas. In this way, they ensure that there will be developing fruits in which they can raise their young.

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Left unchecked, the weevil larvae readily consume all of the developing seeds within the pod, an unfortunate blow to the reproductive efforts of this tiny orchid. However, the situation changes when parasitoid wasps enter the mix. The wasps are also looking for a place to rear their young but the wasp larvae do not eat orchid seeds. Instead, the wasps must find juicy weevil larvae in which to lay their eggs. When the wasp larvae hatch out, they eat the weevil larvae from the inside out and this is where things get really interesting.

The wasp larvae develop at a much faster rate than do the weevil larvae. As such, they kill the weevil long before it has a chance to eat all of the orchid seeds. By doing so, the wasp has effectively rescued the orchids reproductive effort. Over a five year period, researchers based out of the University of Campinas found that orchid fruits in which wasp larvae have killed off the weevil larvae produced nearly as many seeds as uninfected fruits. As such, the parasitoid wasps have made effective pollinators out of otherwise destructive herbivorous weevils.

The fact that a third party (in this case a parasitic wasp) can change a herbivore into an effective pollinator is quite remarkable to say the least. It reminds us just how little we know about the intricate ways in which species interact and form communities. The authors note that even though pollination in this case represents selfing and thus reduced genetic diversity, it nonetheless increases the reproductive success of an orchid that naturally experiences low pollination rates to begin with. In the hyper diverse and competitive world of Brazilian rainforests, even self-pollination cab be a boost for this orchid.

Photo Credits: [1] [2]

Further Reading: [1]

An Endangered Iris With An Intriguing Pollination Syndrome

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The Golan iris (Iris hermona) is a member of the Oncocyclus section, an elite group of 32 Iris species native to the Fertile Crescent region of southwestern Asia. They are some of the showiest irises on the planet. Sadly, like many others in this section, the Golan iris is in real danger of going extinct.

The Golan iris has a rather limited distribution. Despite being named in honor of Mt. Hermon, it is restricted to the Golan Heights region of northern Israel and southwestern Syria. Part of the confusion stems from the fact that the Golan iris has suffered from a bit of taxonomic uncertainty ever since it was discovered. It is similar in appearance to both I. westii and I. bismarckiana with which it is frequently confused. In fact, some authors still consider I. hermona to be a variety of I. bismarckiana. This has led to some serious issues when trying to assess population numbers. Despite the confusion, there are some important anatomical differences between these plants, including the morphology of their rhizomes and the development of their leaves. Regardless, if these plants are in fact different species, it means their respective numbers in the wild decrease dramatically. 

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Like other members of the Oncocyclus group, the Golan iris exhibits an intriguing pollination syndrome with a group of bees in the genus Eucera. Their large, showy flowers may look like a boon for pollinators, however, close observation tells a different story. The Golan iris and its relatives receive surprisingly little attention from most of the potential pollinators in this region.

One reason for their lack of popularity has to do with the rewards (or lack thereof) they offer potential visitors. These irises produce no nectar and very little pollen. Because of this and their showy appearance, most pollinators quickly learn that these plants are not worth the effort. Instead, the only insects that ever pay these large blossoms any attention are male Eucerine bees. These bees aren't looking for food or fragrance, however. Instead, they are looking for a place to rest. 

 A Eucerine bee visiting a nectar source. 

A Eucerine bee visiting a nectar source. 

The Oncocyclus irises cannot self pollinate, which makes studying potential pollinators a bit easier. During a 5 year period, researchers noted that male Eucerine bees were the only insects that regularly visited the flowers and only after their visits did the plants set seed. The bees would arrive at the flowers around dusk and poke around until they found one to their liking. At that point they would crawl down into the floral tube and would not leave again until morning. The anatomy of the flower is such that the bees inevitably contact stamen and stigma in the process. Their resting behavior is repeated night after night until the end of the flowering season and in this way pollination is achieved. Researchers now believe that the Golan iris and its relatives are pollinated solely by these sleeping male bees.

Sadly, the status of the Golan iris is rather bleak. As recent as the year 2000, there were an estimated 2,000 Golan irises in the wild. Today that number has been reduced to a meager 350 individuals. Though there is no single smoking gun to explain this precipitous decline, climate change, cattle grazing, poaching, and military activity have exacted a serious toll on this species. Plants are especially vulnerable during drought years. Individuals stressed by the lack of water succumb to increased pressure from insects and other pests. Vineyards have seen an uptick in Golan in recent years as well, gobbling up viable habitat in the process.

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It is extremely tragic to note that some of the largest remaining populations of Golan irises can be found growing in active mine fields. It would seem that one of the only safe places for these endangered plants to grow are places that are extremely lethal to humans. It would seem that our propensity for violent tribalism has unwittingly led to the preservation of this species for the time being.

At the very least, some work is being done not only to understand what these plants need in order to germinate and survive, but also assess the viability of relocated plants that are threatened by human development. Attempts at transplanting individuals in the past have been met with limited success but thankfully the Oncocyclus irises have caught the eye of bulb growers around the world. By sharing information on the needs of these plants in cultivation, growers can help expand on efforts to save species like the Golan iris.

Photo Credits: [1] [2] [3] [4]

Further Reading: [1] [2] [3] [4]

 

California Bumblebee Decline Linked to Feral Honeybees

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Worldwide, pollinators are having a rough go of it. Humans have altered the landscape to such a degree that many species simply can't keep up. The proverbial poster child for pollinator issues is the honeybee (Apis mellifera). As a result, countless native pollinators get the short shrift when it comes to media attention. This isn't good because outside of intense industrial agriculture, native pollinators make up the bulk of pollination services. Similarly, honeybee fandom often overshadows any potential negative effects these introduced insects might be having on native pollinators.

Long term scientific investigations are starting to paint a more nuanced picture of the impact introduced honeybees are having on native ecosystems. For instance, research based out of California is finding that honeybees are playing a big role in the decline of native bumblebee populations. What's more, these negative impacts are only made worse in the light of climate change.

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For over 15 years, ecologist Dr. Diane Thompson has been studying bumblebee populations in central California. At no point during those early years did any of the bumblebee species she focuses on show signs of decline. In fact, they were quite common. Then, around the year 2000, feral honeybees started to establish themselves in the area. Honeybee colonies were becoming more and more numerous each and every year and that is when she started noticing changes in bumblebee behavior and numbers.

You see, honeybees are extremely successful foragers. They are generalists, which means they can visit a wide variety of flower types. As a result, they are extremely good at competing for floral resources compared to native bumblebees. Her results show that increases in the number of honeybee colonies caused not only a reduction in foraging among the native bumblebees, they also caused a reduction in bumblebee colony success. The native bumblebees simply weren't raising as many young as they were before honeybees entered the system.

 Decreased rainfall cause a decline in flower densities of  Scrophularia californica , a key resource for native bumblebees in this system.

Decreased rainfall cause a decline in flower densities of Scrophularia californica, a key resource for native bumblebees in this system.

Climate change is only making things worse. As drought years become not only more severe but also more intense, the amount of flowers available during the growing season also declines. With fewer flowers on the landscape, bumblebees and honeybees are forced into closer proximity for foraging and the clear winner in most foraging disputes are the tenacious honeybees. As such, bumblebees are chased off the already diminishing floral displays. By 2014, Dr. Thompson had quantified a significant decline in native bumblebee populations as a result.

It would be all too convenient to say that this research represents an isolated case. It does not. More and more research is finding that honeybees frequently out-compete native pollinators for resources such as food and nesting sites. Such effects are especially pronounced in rapidly changing ecosystems. Although honeybees are here to stay, it is important that we realize the impacts that these feral insects are having on our native ecosystems and begin to better appreciate and facilitate the services provided by our native pollinators. 

Photo Credits: [1] [2] [3]

Further Reading: [1] [2] [3] [4]

On the Ecology of Krameria

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There is something satisfying about saying "Krameria." Whereas so many scientific names act as tongue twisters, Krameria rolls of the tongue with a satisfying confidence. What's more, the 18 or so species within this genus are fascinating plants whose lifestyles are as exciting as their overall appearance. Today I would like to give you an overview of these unique parasitic plants.

Commonly known as rhatany, these plants belong to the family Krameriaceae. This is a monotypic clade, containing only the genus Krameria. Historically there has been a bit of confusion as to where these plants fit on the tree of life. Throughout the years, Krameria has been placed in families like Fabaceae and Polygalaceae, however, more recent genetic work suggests it to be unique enough to warrant a family status of its own. 

Regardless of its taxonomic affiliation, Krameria is a wonderfully specialized genus of plants with plenty of offer the biologically curious among us. All 18 species are shrubby, though at least a couple species can sometimes barely qualify as such. They are a New World taxon with species growing native as far south as Paraguay and Chile and as far north as Kansas and Colorado. They generally inhabit dry habitats.

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As I briefly mentioned above, most if not all of the 18 species are parasitic in nature. They are what we call "hemiparasites" in that despite stealing from their hosts, they are nonetheless fully capable of photosynthesis. It is interesting to note that no one has yet been able to raise these plants in captivity without a host. It would seem that despite being able to photosynthesize, these plants are rather specialized parasites. 

That is not to say that they have evolved to live off of a specific host. Far from it actually. A wide array of potential hosts, ranging from annuals to perennials, have been identified. What I find most remarkable about their parasitic lifestyle is the undeniable advantage it gives these shrubs in hot, dry environments. Research has found that despite getting a slow start on growing in spring, the various Krameria species are capable of performing photosynthesis during extremely stressful periods and for a much longer duration than the surrounding vegetation. 

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The reason for this has everything to do with their parasitic lifestyle. Instead of producing a long taproot to reach water reserves deep in the soil, these shrubs invest in a dense layer of lateral roots that spread out in the uppermost layers of soil seeking unsuspecting hosts. When these roots find a plant worth parasitizing, they grow around its roots and begin taking up water and nutrients from them. By doing this, Krameria are no longer limited by what water or other resources their roots can find. Instead, they have managed to tap into large reserves that would otherwise be locked away inside the tissues of their neighbors. As such, the Krameria do not have to worry about water stress in the same way that non-parasitic plants do. 

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By far the most stunning feature of the genus Krameria are the flowers. Looking at them it is no wonder why they have been associated with legumes and milkworts. They are beautiful and complex structures with a rather specific pollination syndrome. Krameria flowers produce no nectar to speak of. Instead, they have evolved alongside a group of oil-collecting bees in the genus Centris.

One distinguishing feature of Krameria flowers are a pair of waxy glands situated on each side of the ovary. These glands produce oils that female Centris bees require for reproduction. Though Centris bees are not specialized on Krameria flowers, they nonetheless visit them in high numbers. Females alight on the lip and begin scraping off oils from the glands. As they do this, they inevitably come into contact with the stamens and pistil. The female bees don't feed on these oils. Instead, they combine it with pollen and nectar from other plant species into nutrient-rich food packets that they feed to their developing larvae.  

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Following fertilization, seeds mature inside of spiny capsules. These capsules vary quite a bit in form and are quite useful in species identification. Each spine is usually tipped in backward-facing barbs, making them excellent hitchhikers on the fur and feathers of any animal that comes into contact with them.  

Photo Credits: [1] [2] [3] [4] [5]

Further Reading: [1] [2] [3] [4]

The Traveler's Palm

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This nifty looking tree is commonly referred to as the traveler's palm (Ravenala madagascariensis). In reality, it is not a palm at all but rather a close cousin of the bird of paradise plants (Strelitziaceae). It is endemic to Madagascar and the only member of its genus. Even more fascinating is its relationship with another uniquely Malagascan group - the lemurs. But first we must ask, what's in a name?

The name "traveler's palm" has two likely explanations. The first has to do with the orientation of that giant fan of leaves. The tree is said to align its photosynthetic fan in an east-west orientation, which can serve as a crude compass, allowing weary travelers to orient themselves. I found no data to support this. The other possibility comes from the fact that this tree collects a lot of water in its nooks and crannies. Each of its hollow leaf bases can hold upwards of a quart of rain water! Get to it quick, though, because these water stores soon stagnate.

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Flowers are produced between the axils of the leaves and closely resemble those of its bird of paradise cousins. Closer observation will reveal that they are nonetheless quite unique. For starters, they are large and contained within stout green bracts. Also, they are considerably less showy than the rest of the family. They don't produce any strong odors but they do fill up with copious amounts of sucrose-rich nectar. Finally, the flowers remain closed, even when mature and are amazingly sturdy structures. It may seem odd for a plant to guard its flowers so tightly until you consider how they are pollinated.

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It seems fitting that an endemic plant like the traveler's palm would enter into a pollination syndrome with another group of Madagascar endemics. As it turns out, lemurs seem to be the preferred pollinators of this species. Though black lemurs, white fronted lemurs, and greater dwarf lemurs have been recorded visiting these blooms, it appears that the black-and-white ruffed lemur manages a bulk of the pollination services for this plant.

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Watching the lemurs feed, one quickly understands why the flowers are so stout. Lemurs force open the blooms to get at the nectar inside. The long muzzle of the black-and-white ruffed lemur seem especially suited for accessing the energy-rich nectar within. The flowers themselves seem primed for such activity. The enclosed anthers are held under great tension. When a lemur pries apart the petals, the anthers spring forward and dust its muzzle with pollen. Using both its hands and feet, the lemur must wedge its face down into the nectar chamber in order to take a sip. In doing so, it inevitably comes into contact with the stigma. Thus, pollination is achieved. Once fertilized, the traveler's palm produces seeds that are covered in beautiful blue arils.

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All in all, this is one unique plant. Though its not the only plant to utilize lemurs as pollinators, it is nonetheless one of the more remarkable examples. Its stunning appearance has made it into something of a horticultural celebrity and one can usually find the traveler's palm growing in larger botanical gardens around the world. Though the traveler's palm itself is not endangered, its lemur pollinators certainly are. As I have said time and again, plants do not operate in a vacuum. To save a species, one must consider the entirety of its habitat. This is why land conservation is so vitally important. Support a land conservancy today!

Photo Credits: [1] [2]

Further Reading: [1] [2] [3]

 

Cockroaches & Unexpected Partnerships

Say "cockroach" and most people will start to squirm. These indefatigable insects are maligned the world over because of a handful of species that have settled in quite nicely among human habitats. The world of cockroaches is far more diverse than most even care to realize, and where they occur naturally, these insects provide important ecological services. For instance, over the last decade or so, researchers have added pollination and seed dispersal to the list of cockroach activities. 

That's right, pollination and seed dispersal. It may seem odd to think of roaches partaking in such interactions but a study published in 2008 provides some of the first evidence that roaches are doing more with plants than eating their decaying tissues. After describing a new species of Clusia in French Guiana, researchers set out to investigate what, if anything, was pollinating it. The plant was named Clusia sellowiana and its flowers emitted a strange scent. 

 Cockroach pollinating  C. sellowiana

Cockroach pollinating C. sellowiana

The source of this scent was the chemical acetoin. It seemed to be a rather attractive scent as a small variety of insects were observed visiting the flowers. However, only one insect seemed to be performing the bulk of pollination services for this new species - a small cockroach called Amazonia platystylata. It turns out that the roaches are particularly sensitive to acetoin and although they don't have any specific anatomical features for transferring pollen, their rough exoskeleton nonetheless picks up and deposits ample amounts of the stuff. 

It would appear that C. sellowiana has entered into a rather specific relationship with this species of cockroach. Although this is only the second documentation of roach pollination, it certainly suggests that more attention is needed. This Clusia isn't alone in its interactions with cockroaches either. As I hinted above, roaches can now be added to the list of seed dispersers of a small parasitic plant native to Japan. 

 (A) M. humile fruit showing many minute seeds embedded in the less juicy pulp. (B) Fallen fruits. (C) Blattella nipponica feeding on the fruit. (D) Cockroach poop with seeds. (E) Stained cockroach-ingested seeds

Monotropastrum humile looks a lot like Monotropa found growing in North America. Indeed, these plants are close cousins, united under the family Ericaceae. Interestingly enough, it was only recently found that camel crickets are playing an important role in the seed dispersal of this species. However, it looks like they aren't the only game in town. Researchers have also found that a forest dwelling cockroach called Blattella nipponica serves as a seed disperser as well. 

The roaches were observed feeding on the fruits of this parasitic plant, consuming pulp and seed alike. What's more, careful observation of their poop revealed that seeds of M. humile passed through the digestive tract unharmed. Cockroaches can travel great distances and therefore may provide an important service in distributing the seeds of a rather obscure parasitic plant. To think that this is an isolated case seems a bit naive. It seems to me like we should pay a little more attention to what cockroaches are doing in forests around the world. 

Photo Credits: [1] [2] [3]

Further Reading: [1] [2]

Resin Midges, Basal Angiosperms, and a Strange Pollination Syndrome

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When we try to talk about clades that are "basal" or "sister" to large taxonomic groups, your average listener either consciously or unconsciously thinks "primitive." Primitive has connotations of something that under-developed or unfinished. This is simply not the case. Take, for instance, a family of basal angiosperms called Schisandraceae.

This family is nestled within the order Austrobaileyales, which, along with a small handful of other families, represent the earliest branches of the angiosperm family tree still alive today.  To call them primitive, however, would be a serious misnomer. Because they diverged so early on, these lineages represent serious success stories in flowering plant evolution, having survived for hundreds of millions of years. Instead, we must think of them as fruitful early experiments in angiosperm evolution.

Floral morphology of and interaction between midge and their larvae (white arrows) in Illicium dunnianum

Still, the proverbial proof is in the pudding and if there was any sort of physical evidence one could put forth to remove our hierarchical prejudices about the taxonomic position of these plants, it would have to be their bizarrely specific pollination syndromes.  Members of the family Schisandraceae have entered into intense relationships with a group of flies known as midges and their interactions are anything but primitive. 

We will start with two species of plant native throughout parts of Asia. Meet as Illicium dunnianum and Illicium tsangii. More will be familiar with this genus than they may realize as Illicium gives us the dreaded star anise flavor our grandparents liked to sneak into our cookies as kids (but I digress). These particular species, however, have more to offer the world than flavoring. They are also very important plants for a group of gall midges in the genus Clinodiplosis.

The midges cannot reproduce without I. dunnianum or I. tsangii. You see, these midges lay their eggs within the flowers of these plants and, in doing so, end up pollinating them in the process. At first glance it may seem like a very one-sided relationship. Female midges deposit their eggs all along the carpels packed away inside large, fleshy whorl of tepals. As the midges crawl all over the reproductive organs looking for a suitable place to lay, they inevitably pick up and deposit pollen. 

Floral morphology and interaction between midge larvae (white arrows) in  Illicium tsangii

This is not the end of this relationship though. After eggs have been deposited, something strange happens to the Illicium flowers. For starters, they develop nursery chambers around the midge larvae. Additionally, their tepals begin producing heat. Enough heat is produced to keep the nursery chamber temperature significantly warmer than the ambient air temperature. What's more flower heating intensifies throughout the duration of fruit development. It was originally hypothesized that this heating had something to do with floral odor volatilization and seed incubation, however, experiments have shown that at least seed development in these two shrubs is not influenced by floral heat in any major way. The same cannot be said for the midge larvae. 

As the flowers mature and give way to developing seeds, the midge larvae are hard at work feeding on tiny bits of the flowers themselves. When researchers looked at midge larvae development on these Illicium species, they found that they were completely dependent upon the floral heat for survival. Any significant drop in temperature caused them to die. Essentially, the plants appear to be producing heat more for the midges than for themselves. It may seem odd that these two plants would invest so much energy to heat their flowers so that midge larvae feeding on their tissues can survive but such face-value opinions rarely stand in ecology.

One must not forget that those larvae grow up to be adult midges that will go on to pollinate the Illicium flowers the following season. Although the plants are taking a bit of a hit by allowing the larvae to develop within their tissues, they are nonetheless ensuring that enough pollinators will be around to repeat the process again. If that wasn't cool enough, the relationship between each of these plants and their pollinators are rather specific and the authors of at least one paper believe that the midges that pollinate each species are new to science. 

Now, if I haven't managed to convince you that this angiosperm sister lineage is anything but primitive, then let's take a look at another genus within the family Schisandraceae that have taken this midge pollination syndrome to the next level. This story also takes place in Asia but instead involves a genus of woody vines known as Kadsura

Like the Illicium we mentioned earlier, a handful of Kadsura species rely on midges for pollination. The way in which they go about maintaining this relationship is a bit more involved. The midges that are attracted by Kadsura flowers are known as resin midges and their larvae live off of plant resins. The flowers of Kadsura are another story entirely. They are as odd as they are beautiful. 

 Flowers, pollinators ,and their larvae (white arrows) in  Kadsura heteroclita .

Flowers, pollinators ,and their larvae (white arrows) in Kadsura heteroclita.

In male flowers, stamens are arranged in dense, cone-like structures called androecia whereas the female flowers contain a compact shield-like structure with the uppermost part of the stigma barely emerging. This is called a gynoecium. Even weirder, the male flowers of one particularly strange species, Kadsura coccinea, produce large, swollen inner tepals. 

Once Kadsura flowers begin to open, visiting midges are not far behind. Male flowers seem to attract more midges than female flowers and it is thought that this has to do with varying amounts of special attractant chemicals produced by the flowers themselves. Regardless, midges set to work exploring the blooms with males looking for mates and females looking for a place to lay their eggs. 

When a suitable spot has been found, females will deposit their eggs into the floral tissues with their ovipositor. The wounded plant tissues immediately begin producing resin, not unlike a wounded pine tree. In the case of K. coccinea, it would appear that the oddly swollen tepals are specifically targeted by female midges for egg laying. They too produce resin upon having eggs laid within. 

The oddball flowers of Kadsura coccinea showing swollen tepals.

The function of plant resins in many cases are to fight off pathogens. From beetles to fungi, resin helps plug up and seal off wounds. This does not seem to be the case in the Kadsura-midge relationship though. The so-called "brood chambers" within the floral tissues go on producing resin for upwards of 6 days after the midge eggs were laid. Eventually the floral parts whither and drop off but the midge larvae seem to be quite happy in their resin-filled homes. 

As it turns out, the resin midge larvae feed on the viscous resin as their sole food source. Instead of trying to ward off these pesky little insects, the plants seem to be encouraging them to raise their offspring within! Just as we saw in the Asian Illicium, these Kadsura vines seem to be providing brood sites for their pollinators. Also, just as the Illicium-midge relationship thought to be species specific, each species of Kadsura appears to have its own specific species of resin midge pollinator! K. coccinea even goes as far as to produce tepals specifically geared towards raising midge larvae, thus keeping them away from their more valuable reproductive organs. In return for the nursery service, Kadsura have their pollinators all to themselves.

Pollination mutualisms in which plants trade raising larvae for pollen transfer are extremely derived and some of the most specialize plant/animal interactions on the planet. To find such relationships in these basal or sister lineages is living proof that these plants are anything but primitive. In the energy-reproductive investment trade-off, it appears that ensuring ample pollinator opportunities far outweighs the cost of providing them with nursery chambers. It is remarkable to think just how intertwined the relationships between these plants and there pollinators truly are. Take that, plant taxonomic prejudices! 

Photo Credits: [1] [2]

Further Reading: [1] [2] 

 

A Common Plant With An Odd Pollination Mechanism

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Pollination is not an altruistic enterprise. Each party involved is trying to maximize its gains while minimizing its losses. Needless to say, cheaters abound in natural systems. As such, plants have gone to great lengths to ensure that their reproductive investments pay off in the long run. Take, for instance, the case of the fragrant water-lily (Nymphaea odorata). 

Most of us have encountered this species at some point in our lives. Those who have often remark on the splendor of their floral displays. Certainly this is not lost on pollinators either. Coupled with their aromatic scent, these aquatic plants must surely be a boon to any insect looking for pollen and nectar. Still, the flowers of the fragrant water-lily take no chances.

Close observation will reveal an interesting pattern in the blooming cycle of this water-lily. On the first day that the flowers open, only the female portions are mature. The structure itself is bowl-like in shape. Filling this stigmatic bowl is a viscous liquid. After the first day, the flowers close for the evening and reopen to reveal that the stigma is no longer receptive and instead, the anthers have matured.

Many insects will visit these floating flowers throughout the blooming period. Everything from flies, to beetles, and various sorts of bees have been recorded. Seed set in this species is pollen limited so any insect visiting a female flower must deposit pollen if reproduction is to be achieved. This is where that bowl of sticky liquid comes into play. The liquid itself is rather unassuming until you see an insect fall in.

Due to the presence of surfactants, any insect that falls into the fluid immediately sinks to the bottom. The flowers seem primed to encourage this to happen too. The flexible inner stamens that surround the bowl bend under the weight of heavier insects, thus dumping them into the liquid below. Only by observing this process under extreme magnification does all of this make sense.

The liquid within the bowl essentially washes off any pollen that a visiting insect had stuck to its body. As the pollen falls off, it drifts down to the bottom of the bowl where it contacts the receptive stigma. Thus, cross-pollination is achieved. Most of the time, insect visitors are able to crawl out without any issue. However, the occasional insect will drown within the fluid. Alas, that is no sweat off the water-lily's back. Having dropped off the pollen it was carrying, it is of little use to that flower anymore.

Once a water-lily flower has been fertilized, its stem begins to curl up like a spring. This draws the ovaries underwater where they can develop in relative safety. It also ensures that, upon maturing, the seeds are more likely to find a suitable underwater site for germination. To think that this drama plays out time and time again unbeknownst to the casual observer is something I find endlessly fascinating about the natural world.

Photo Credit: [1] [2]

Further Reading: [1] [2]