An Endemic Spurge in Florida

A pistillate cyathium of a Telephus spurge.

A pistillate cyathium of a Telephus spurge.

Endemism fascinates me. Why some organisms occur in certain restrict areas geographically and nowhere else is such a fun topic to ponder. On a recent trip to the Florida Panhandle, I was lucky enough to encounter a wonderful little plant endemic to pine flatwoods located at the very tip of the Apalachicola region. It is a type of spurge known as Telephus spurge (Euphorbia telephioides) whose natural history is captivating to say the least.

The Telephus spurge is a denizen of dry, sandy soils. Its fleshy leaves and deep, tuberous taproot not only allow it to handle drought via the storage of water and nutrients, its root system also allows it to live a long time. Though it is hard to say how long individuals can actually live, lifetimes measured in decades are well within the realm of possibility. Like many members of the spurge family (Euphorbiaceae), the Telephus spurge is also well defended by toxic, milky sap.

A staminate cyathium of a Telephus spurge.

A staminate cyathium of a Telephus spurge.

The inflorescence of the Telephus spurge is defined as a cyathium. Plants can produce multiple cyathia per plant, and for the Telephus spurge, these can contain only male, only female, or both reproductive structures. Sex of individual Telephus spurge is an interesting topic unto itself and very important when it comes to conservation (more on that in a bit). Individual Telephus spurge can be fluid in their sexual expression from one year to the next. Individuals that produced only male cyathia one year can go on to produce only female or bisexual cyathia in subsequent years. No one can say for sure what triggers these changes among individuals, but disturbance and energy reserves likely play a considerable role.

One of the most important aspects of Telephus spurge ecology is fire. Without regular fires, the entire habitat of the Telephus spurge would gradually close in with woody shrubs and trees and disappear. Even though most of the top parts of these plants are killed by fires, their large tuberous root system allows them to readily regrow what was lost. That is not to say that individuals regularly regrow after fires. In fact, plants have been known to disappear for years at a time following top killing events, only to resprout at some point in the future when favorable conditions return.

Telephus spurge fruits are quite pretty!

Telephus spurge fruits are quite pretty!

At this point, it should be obvious that for this species to persist, its habitat needs to be maintain via fire. Management for this species is very important given its narrow distribution and sporadic occurrence on the landscape. However, there are still many hurdles in the way of effective Telephus spurge conservation. For starters, though it once likely enjoyed a more contiguous distribution throughout the Apalachicola region, habitat destruction from logging, ditching, and development have highly fragmented its populations into tiny clusters. The smaller these clusters become, the more vulnerable they are to extirpation.

Another factor complicating the conservation of this species is its aforementioned sexual fluidity. Because we still don’t know what triggers a change in sexual expression among individuals from one year to the next, populations can fluctuate greatly in terms of their reproductive capacity. For instance, if a population comprised of many individuals with bisexual cyathia one year suddenly switches to producing mostly male cyathia the following year, seed production can decrease greatly. Until we know more about the reproductive ecology of this species, maintaining populations with regular fire while limiting the amount of logging and development is the best chance we have at ensuring this extremely rare spurge has a future on this planet.

The one upside to this story is that, where properly managed, Telephus spurge can reach high abundances. With a little bit of effort, these populations are relatively easy to map and seed can be collected and maintained to preserve valuable genetic material. Still, without proper management and land conservation/restoration efforts, the future of this tiny spurge and many of its botanical neighbors hangs in the balance. Support your local land conservancy today, because stories like this are far more common than you think!

Further Reading: [1] [2]



My Unforgettable Encounter with a Fevertree

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When someone asks you if you would like to see a wild fever tree, you have to say yes. As a denizen of cold climates defined by months of freezing temperatures, I will never miss an opportunity to encounter any species in its native habitat that cannot survive frosts. This was the scenario I found myself in last week as friend and habitat restoration specialist for the Atlanta Botanical Garden, Jeff Talbert, was showing us around a wonderful chunk of Florida scrubland he has been managing over the last few years.

He drove our small group over to an area that, up until a year or two ago, was completely choked with swamp titi (Cyrilla racemiflora). Like many habitats throughout southeastern North America, this patch of Florida scrub is dependent on regular fires to maintain ecological function. Without it, aggressive shrubs like titi completely take over, choking out much of the amazing biodiversity that makes this region unique. Jeff and his team have been very busy restoring fire to this ecosystem and the results have been impressive to say the least.

We walked off the two-track, down into a wet depression and were greeted by an impressive population of spoon-leaf sundews (Drosera intermedia), which is a good sign that water quality on the site is improving. After a few minutes of sundew admiration, Jeff motioned for us to look upward towards the surrounding tree line. That’s when we saw it. Growing up out of the small seep that was feeding this wet depression was a spindly tree with bright pink splotches decorating its canopy. This was to be my first encounter with a fevertree (Pinckneya bracteata).

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A few of us were willing to get our feet wet and were rewarded with a close look at the growth habit of this incredible tree. Clustered at the end of its spindly branches are dark green, ovate leaves that give the tree a tropical appearance. Erupting from the middle of some of those leafy branches were the inflorescences. These are what produce the pink splotches I could see in the canopy of larger individuals. They remind me a lot of a poinsettia and at first, I thought this tree might be a member of the genus Euphorbia. Indeed, the pink coloration comes from a handful of rather large, leaf-like sepals attached to the base of each inflorescence.

Upon seeing the flowers, I instantly knew this was not a member of Euphorbiaceae. Each flower was long and tubular ending in five reflexed lobes. They are colorful structures in and of themselves, adorned with splashes of pink and yellow. After a bit of scrutiny, our group was finally able to place this within its true taxonomic lineage, the coffee family (Rubiaceae).

Within the coffee family, fevertree is closely related to the genus Cinchona. Like Cinchona, the fevertree produces quinine and other alkaloids that are effective in treating malaria. Fevertree has been used for millennia to do just that, hence the common name. It also seems fitting that fevertrees tend to grow in wetland habitats where mosquitos can be abundant. However, this is by no means an obligate wetland species. Those who have grown fevertree frequently succeed in establishing plants in dry, upland habitats as well. Perhaps highly disturbed wetlands are some of the few places where this spindly tree can avoid intense competition from other forms of vegetation.

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Fevertrees do need regular disturbance to persist. They are not a large, robust tree by any means and can easily get outcompeted by more aggressive vegetation. However, this species does have a trick that enables individuals to persist when disturbances don’t come frequent enough. Fevertree is highly clonal. Instead of producing a single trunk, it sends out numerous stems in all directions in search of a gap in the canopy. This clonal habit allows it to eek out an existence in the gaps between its more robust neighbors until disturbances return and clear things out.

This clonal habit is also very important when it comes to reproduction. Fevertree requires a decent amount of sunlight to successfully flower and set seed. By using its clonal stems to find light gaps, it can at least guarantee some level of reproduction until fires, floods, or some other form of canopy clearing disturbance frees up enough space for it to prosper and its seeds to germinate. However, its clonal habit can also hurt its reproductive capacity over the long term if recruitment of new individuals does not occur.

Fevertree is considered self-incompatible. In other words, its flowers cannot be pollinated via pollen from a genetically identical individual. As more and more clonal shoots are produced, the tree effectively increases the chances that its own pollen will end up on its own flowers. This is yet another important reason why regular disturbance favors fevertree reproduction. Fevertree seeds need light and bare ground to germinate, which is usually provided as fires and other disturbances clear the canopy and open up bare ground. Only then can enough unrelated individuals establish to ensure plenty of successful pollination opportunities.

With its long, tubular flowers and bright pink sepals, fevertrees don’t seem to have any trouble attracting pollinators, which mainly consist of ruby-throated hummingbirds and bumblebees. Only these organisms have what it takes to successfully access the pollen and nectar rewards of this plant and travel the distances necessary to ensure pollen ends up on unrelated individuals. The seeds that result from pollination are winged and can travel a decent distance with a decent wind. With any luck, a few seeds will end up in another disturbance-cleared wet area and usher in the next generation of fevertrees.

I am so happy that restoration activities at this site are making more suitable habitat for this unique tree. Looking around, we saw many more small individuals starting to emerge where there was once a dense canopy of titi. Hopefully with ongoing management, this population will continue to grow and spread, securing the a future for this species in a region with an ever-growing human presence. If you ever find the opportunity to see one of these trees in person, do yourself a favor and take it!

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

The Future of New Zealand's Shrubby Tororaro Lies in Cultivation

Photo by Jon Sullivan licensed under CC BY-NC 2.0

Photo by Jon Sullivan licensed under CC BY-NC 2.0

I was watching a gardening show hosted by one of my favorite gardeners, Carol Klein, when she introduced viewers to a beautiful, divaricating shrub whose branching structure looked like a dense tracery of orange twigs. She referred to the shrub as a wiggy wig and remarked on its beauty and form before moving on to another wonderful plant. I was taken aback by the structure of the shrub and had to learn more. Certainly its form had to be the result of delicate pruning and selective breeding. Imagine my surprise when I found its growth habit was inherent to this wonderful and rare species.

The wiggy wig or shrubby tororaro is known to science as Muehlenbeckia astonii. It is a member of the buckwheat family (Polygonaceae) endemic to grey scrub habitats of eastern New Zealand. Though this species is widely cultivated for its unique appearance, the shrubby tororaro is not faring well in the wild. For reasons I will cover in a bit, this unique shrub is considered endangered. To understand some of these threats as well as what it will take to bring it back from the brink, we must first take a closer look at its ecology.

Photo by WJV&DB licensed under CC BY-SA 3.0

Photo by WJV&DB licensed under CC BY-SA 3.0

As mentioned, the shrubby tororaro is endemic to grey scrub habitats of eastern New Zealand. It is a long lived species, with individuals living upwards of 80 years inder the right conditions. Because its habitat is rather dry, the shrubby tororaro grows a deep taproot that allows it to access water deep within the soil. That is not to say that it doesn’t have to worry about drought. Indeed, the shrubby tororaro also has a deciduous habit, dropping most if not all of its tiny, heart-shaped leaves when conditions become too dry. During the wetter winter months, its divaricating twigs become bathed in tiny, cream colored flowers that are very reminiscent of the buckwheat family. From a reproductive standpoint, its flowers are quite interesting.

The shrubby tororaro is gynodioecious, which means individual shrubs produce either only female flowers or what is referred to as ‘inconstant male flowers.’ Essentially what this means is that certain individuals will produce some perfect flowers that have functional male and female parts. This reproductive strategy is thought to increase the chances of cross pollination among unrelated individuals when populations are large enough. Following successful pollination, the remaining tepals begin to swell and surround the hard nut at the center, forming a lovely translucent fruit-like structure that entices dispersal by birds. As interesting and effective as this reproductive strategy can be in healthy populations, the shrubby tororaro’s gynodioecious habit starts to break down as its numbers decrease in the wild.

Photo by Jon Sullivan licensed under CC BY-NC 2.0

Photo by Jon Sullivan licensed under CC BY-NC 2.0

As New Zealand was colonized, lowland habitats like the grey scrub were among the first to be converted to agriculture and that trend has not stopped. What grey scrub habitat remains today is highly degraded by intense grazing and invasive species. Habitat loss has been disastrous for the shrubby tororaro and its neighbors. Though this shrub was likely never common, today only a few widely scattered populations remain and most of these are located on private property, which make regular monitoring and protection difficult.

Observations made within remnant populations indicate that very little reproduction occurs anymore. Either populations are comprised of entirely female individuals or the few inconstant males that are produced are too widely spaced for pollination to occur. Even when a crop of viable seeds are produced, seedlings rarely find the proper conditions needed to germinate and grow. Invasive grasses and other plants shade them out and invasive insects and rodents consume the few that manage to make it to the seedling stage. Without intervention, this species will likely go extinct in the wild in the coming decades.

Photo by John Pons licensed under CC BY-SA 4.0

Photo by John Pons licensed under CC BY-SA 4.0

Luckily, conservation measures are well underway and they involve cultivation by scientists and gardeners alike. There is a reason this shrub has become very popular among gardeners - it is relatively easy to grow and propagate. From hardwood cuttings taken in winter, the shrubby tororaro will readily root and grow into a clone of the parent plant. Not only has this aided in spreading the plant among gardeners, it has also allowed conservationists to preserve and bolster much of the genetic diversity within remaining wild populations. By cloning, growing, and distributing individuals among various living collections, conservationists have at least safeguarded many of the remaining individuals.

Moreover, cultivation on this scale means dwindling wild populations can be supplemented with unrelated individuals that produce both kinds of flowers. By increasing the numbers within each population, conservationists are also decreasing the distances between female and inconstant male individuals, which means more chances for pollination and seed production. Though by no means out of the proverbial woods yet, the shrubby tororaro’s future in the wild is looking a bit brighter.

This is good news for biodiversity of the region as well. After all, the shrubby tororaro does not exist in a vacuum. Numerous other organisms rely on this shrub for their survival. Birds feed heavily on its fruits and disperse its seeds while the larvae of at least a handful of moths feed on its foliage. In fact, the larvae of a few moths utilize the shrubby tororaro as their sole food source. Without it, these moths would perish as well. Of course, those larvae also serve as food for birds and lizards. Needless to say, saving the shrubby tororaro benefits far more than just the plant itself. Certainly more work is needed to restore shrubby tororaro habitat but in the meantime, cultivation is ensuring this species will persist into the future.

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

The Knife-Edge Economy of Panama's Trash-Basket Treelet

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Trade-offs abound in nature. It would be impossible for any organism to evolve a combination of attributes that are ideal under all circumstances. This is especially true for plants. The botanical world’s need to obtain water and nutrients from roots while simultaneously maximizing photosynthetic area often means finding a balance between allocating resources to leaves and roots. This trade-off is made especially apparent in species like Panama’s basurera (Quadrella antonensis), whose name translates to trash basket.

The basurera is a rare treelet endemic to only a few highland locations in Panama where it grows in the dense shade of the rainforest canopy. It earned the name basurera because this tiny tree has adopted a litter trapping lifestyle. The few leaves it produces form a basket-like structure at the tip of its spindly stem. As debris falls from the canopy above, some of it is trapped by basurera’s leafy basket. The fact that basurera collects debris isn’t all that shocking. Many understory plants are saddled with a debris load to one degree or another. The most striking feature of its anatomy can be found by digging around in the litter trapped within its leafy basket.

Even “large” basurera are not that big. [SOURCE]

Even “large” basurera are not that big. [SOURCE]

From its tiny stem and branches emerges numerous adventitious roots. These roots branch out into the humus as it builds up within the basket. Not only do the roots help the treelet to hold onto any litter that falls into the basket, they also function just like roots in the soil. As the roots branch and fork, they produce copious fine root hairs. These root hairs have even been found to associate with arbuscular mycorrhizal fungi! Indeed, the basurera is creating its own soil by trapping litter from above that it can use to obtain nutrients that it can’t get from the soil at its base. However, in using its leaves to do this, this treelet puts a damper on its potential photosynthetic capacity.

As humus develops within the basket, it blocks sunlight from hitting the leaves. As you can imagine, this creates a delicate knife-edge economy in this already shady habitat. By manipulating the amount of humus in the basket, scientists have shown that the basurera relies on that humus for sustenance. When the humus was selectively removed, basurera lack the nutrients needed to produce more leaves. However, as humus builds up, the plant photosynthesizes less and less. It would appear that this species has dealing with a trade-off in assimilating carbon and acquiring other forms of nutrients.

Adventitious roots emerging from the stem of a basurera. [SOURCE]

Adventitious roots emerging from the stem of a basurera. [SOURCE]

Research suggests that the shift towards litter trapping likely has to do with the nutrient-poor soils in which the basurera grows. Instead of relying on the ground to provide it with the nutrients it needs, the basurera simply produces its own supply of soil in its leaves. It seems that for this shade-tolerant treelet, obtaining nutrients is more pressing than maximizing photosynthesis. However, in doing so, it is sacrificing growth and reproduction. By studying 112 individuals over the course of a year, scientists found that only 30 basurera actually flowered and, out of those 30, only 10 fruits were produced. Such low reproductive output likely explains why this treelet can only be found in a few areas of Panama. It also makes the basurera extremely vulnerable to disturbance. With slow growth and even slower reproduction, the basurera is at high risk from anything that can reduce population numbers.

Despite its rarity in the highland forests of Panama, the basurera nonetheless offers a window into the economic balance plants must strike as they try to make a living. It just goes to show you that even small, obscure species have a lot to teach us about the evolution of life on our planet.



Photo Credits & Further Reading: [1]

Can Cultivation Save the Canary Island Lotuses?

Photo by VoDeTan2 Dericks-Tan licensed under the GNU Free Documentation License

Photo by VoDeTan2 Dericks-Tan licensed under the GNU Free Documentation License

Growing and propagating plants is, in my opinion, one of the most important skills humanity has ever developed. That is one of the reasons why I love gardening so much. Growing a plant allows you to strike up a close relationship with that species, which provides valuable insights into its biology. In today’s human-dominated world, it can also be an important step in preventing the extinction of some plants. Such may be the case for four unique legumes native to the Canary Islands provided it is done properly.

The Canary Islands are home to an impressive collection of plants in the genus Lotus, many of which are endemic. Four of those endemic Lotus species are at serious risk of extinction. Lotus berthelotii, L. eremiticus, L. maculatus, and L. pyranthus are endemic to only a few sites on this archipelago. Based on old records, it would appear that these four were never very common components of the island flora. Despite their rarity in the wild, at least one species, L. berthelotii, has been known to science since it was first described in 1881. The other three were described within the last 40 years after noting differences among plants being grown locally as ornamentals.

Photo by John Rusk licensed under CC BY 2.0

Photo by John Rusk licensed under CC BY 2.0

All four species look superficially similar to one another with their thin, silvery leaves and bright red to yellow flowers that do a great impression of a birds beak. The beak analogy seems apt for these flowers as evidence suggests that they are pollinated by birds. In the wild, they exhibit a creeping habit, growing over rocks and down overhangs. It is difficult to assess whether their current distributions truly reflect their ecological needs or if they are populations that are simply hanging on in sites that provide refugia from the myriad threats plaguing their survival.

None of these four Lotus species are doing well in the wild. Habitat destruction, the introduction of large herbivores like goats and cattle, as well as a change in the fire regime have seen alarming declines in their already small populations. Today, L. eremiticus and L. pyranthus are restricted to a handful of sites on the island of La Palma and L. berthelotii and L. maculatus are restricted to the island of Tenerife. In fact, L. berthelotii numbers have declined so dramatically that today it is considered nearly extinct in the wild.

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Contrast this with their numbers in captivity. Whereas cultivation of L. eremiticus and L. pyranthus is largely restricted to island residents, L. berthelotii and L. maculatus and their hybrids can be found in nurseries all over the world. Far more plants exist in captivity than in their natural habitat. This fact has not been lost on conservationists working hard to ensure these plants have a future in the wild. However, simply having plants in captivity does not mean that the Canary Island Lotus are by any means safe.

One of the biggest issues facing any organism whose numbers have declined is that of reduced genetic diversity. Before plants from captivity can be used to augment wild populations, we need to know a thing or two about their genetic makeup. Because these Lotus can readily be rooted from cuttings, it is feared that most of the plants available in the nursery trade are simply clones of only a handful of individuals. Also, because hybrids are common and cross-pollination is always a possibility, conservationists fear that the individual genomes of each species may run the risk of being diluted by other species’ DNA.

Photo by VoDeTan2 Dericks-Tan licensed under the GNU Free Documentation License

Photo by VoDeTan2 Dericks-Tan licensed under the GNU Free Documentation License

Luckily for the Canary Island Lotus species, a fair amount of work is being done to not only protect the remaining wild plants, but also augment existing as well as establish new populations. To date, many of the remaining plants are found within the borders of protected areas of the island. Also, new areas are being identified as potential places where small populations or individuals may be hanging on, protected all this time by their inaccessibility. At the same time, each species has been seed banked and entered into cultivation programs in a handful of botanical gardens.

Still, one of the best means of ensuring these species can enjoy a continued existence in the wild is by encouraging their cultivation. Though hybrids have historically been popular with the locals, there are enough true species in cultivation that there is still reason for hope. Their ease of cultivation and propagation means that plants growing in peoples’ gardens can escape at least some of the pressures that they face in the wild. If done correctly, ex situ cultivation could offer a safe haven for these unique species until the Canary Islands can deal with the issues facing the remaining wild populations.

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

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

An Iris With Multiple Parents

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The Abbeville iris (Iris nelsonii) is a very special plant. It is the rarest of the so-called “Louisiana Irises” and can only be found growing naturally in one small swamp in southern Louisiana. If you are lucky, you can catch it in flower during a few short weeks in spring. The blooms come in a range of colors from reddish-purple to nearly brown, an impressive sight to see siting atop tall, slender stems. However, the most incredible aspect of the biology of this species is its origin. The Abbeville iris is the result of hybridization between not two but three different iris species.

When I found out I would be heading to Louisiana in the spring of 2019, I made sure that seeing the Abbeville iris in person was near the top of my to-do list. How could a botany nut not want to see something so special? Iris nelsonii was only officially described as a species in 1966. Prior to that, many believed hybridization played a role in its origin. Multiple aspects of its anatomy appear intermediate between other native irises. It was not until proper molecular tests were done that the picture became clear.

The Abbeville iris genome contains bits and pieces of three other irises native to Louisiana. The most obvious parent was yet another red-flowering species - the copper iris (Iris fulva). It also contains DNA from the Dixie iris (Iris hexagona) and the zig-zag iris (Iris brevicaulis). If you had a similar childhood as I did, then you may have learned in grade school biology class that hybrids are usually biological dead ends. They may exhibit lots of beneficial traits but, like mules, they are often sterile. Certainly this is often the case, especially for hybrid animals, however, more and more we are finding that hybridization has resulted in multiple legitimate speciation events, especially in plants.

Iris fulva. Photo by Richard licensed under CC BY-NC-ND 2.0

Iris fulva. Photo by Richard licensed under CC BY-NC-ND 2.0

Iris hexagona. Photo by beautifulcataya licensed under CC BY-NC-ND 2.0

Iris hexagona. Photo by beautifulcataya licensed under CC BY-NC-ND 2.0

Iris brevicaulis. Photo by peganum licensed under CC BY-SA 2.0

Iris brevicaulis. Photo by peganum licensed under CC BY-SA 2.0

How exactly three species of iris managed to “come together” and produce a functional species like I. nelsonii is interesting to ponder. Each of its three parent species prefers a different sort of habitat than the others. For instance, the copper iris is most often found in seasonally wet, shady bottomland hardwood forests as well as the occasional roadside ditch, whereas the Dixie iris is said to prefer more open habitats like wet prairies. In a few very specific locations, however, these types of habitats can be found within relatively short distances of each other.

Apparently at some point in the past, a few populations swapped pollen and the eventual result was a stable hybrid that would some day be named Iris nelsonii. As mentioned, this is a rare plant. Until it was introduced to other sites to ensure its ongoing existence in the wild, the Abbeville iris was only known to occur in any significant numbers at one single locality. This necessitates the question as to whether or not this “species” is truly unique in its ecology to warrant that status. It could very well be that that single locality just happens to produce a lot of one off hybrids.

In reality, the Abbeville iris does seem to “behave” differently from any of its parental stock. For starters, it seems to perform best in habitats that are intermediate of its parental species. This alone has managed to isolate it enough to keep the Abbeville from being reabsorbed genetically by subsequent back-crossing with its parents. Another mechanism of isolation has to do with its pollinators. The Abbeville iris is intermediate in its floral morphology as well, which means that pollen placement may not readily occur when pollinators visit different iris species in succession. Also, being largely red in coloration, the Abbeville iris receives a lot of attention from hummingbirds.

Although hummingbirds do not appear to show an initial preference when given the option to visit copper and Abbeville irises at a given location, research has found that once hummingbirds visit an Abbeville iris flower, they tend to stick to that species provided enough flowers are available. As such, the Abbeville iris likely gets the bulk of the attention from local hummingbirds while it is in bloom, ensuring that its pollen is being delivered to members of its own species and not any of its progenitors. For all intents and purposes, it would appear that this hybrid iris is behaving much like a true species.

As with any rare plant, its ongoing survival in the wild is always cause for concern. Certainly Louisiana is no stranger to habitat loss and an ever-increasing human population coupled with climate change are ongoing threats to the Abbeville iris. Changes in the natural hydrologic cycle of its swampy habitat appear to have already caused a shift in its distribution. Whereas it historically could be found in abundance in the interior of the swamp, reductions in water levels have seen it move out of the swamp and into ditches where water levels remain a bit more stable year round. Also, if its habitat were to become more fragmented, the reproductive barriers that have maintained this unique species may degrade to the point in which it is absorbed back into an unstable hybrid mix with one or a couple of its parent species. Luckily for the Abbeville, offspring have been planted into at least one other location, which helps to reduce the likelihood of extinction due to a single isolated event.

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

The Creeping Fuchsia

Photo by James Gaither licensed under CC BY-NC-ND 2.0

Photo by James Gaither licensed under CC BY-NC-ND 2.0

Meet Fuchsia procumbens aka the creeping Fuchsia. This lovely plant is endemic to New Zealand where, sadly, it is threatened. In its native habitat, it is strictly a coastal species, prefering to grow in sandy soils. The  flowers are quite unlike most other members of the genus Fuchshia and they exhibit an interesting flowering strategy. 

Fuchsia procumbens produces 3 distinct flower forms, flowers with only  working male parts, flowers with only working female parts, and hermaphroditic flowers. One reason for this is to avoid self-pollination. The other reason may have something to do with energy costs. When growing conditions are less than stellar, the plant saves energy by producing male flowers. 

Photo by Martin Reith licensed under CC BY-SA 4.0

Photo by Martin Reith licensed under CC BY-SA 4.0

Pollen is relatively cheap after all. When conditions improve, the plant may allocate more resources to female and hermaphroditic flowers. This strategy worries some botanists because it seems like some populations of F. procumbens only ever produce single sex flowers. After pollination, the flowers give way to bright red berries that are larger than the flowers themselves!

The most interesting thing about this species is, despite its apparent specificity in habitat preferences in the wild, it competes well with aggressive grasses, which has made it a very popular ground cover. As it turns out, its growing popularity in the garden trade may save this species from being placed on the endangered species list.

Photo Credits: [1] [2]

Further Reading: [1] [2]

The Smallest of the Giants

Photo by Edwino S. Fernando [source]

Photo by Edwino S. Fernando [source]

There are a lot of cool ways to discover a new species but what about tripping over one? That is exactly how Rafflesia consueloae was found. Researchers from the University of the Philippines Los Baños were walking through the forest back in 2014 when one of them tripped over something. To their surprise, it was the bloom of a strange parasitic plant.

This was an exciting discovery because it meant that that strange family of holoparasitic plants called Rafflesiaceae just got a little bit bigger. Rafflesiaceae is famous the world over for the size of its flowers. Whereas the main body of plants in this family consists of tiny thread-like structures living within the tissues of forest vines, the flowers of many are huge. In fact, with a flower 3 feet (1 meter) in diameter, which can weigh as much as 24 lbs. (11 kg), Rafflesia arnoldii  produces the largest flower on the planet. This new species of Rafflesia, however, is a bit of a shrimp compared to its cousins.

In fact, R. consueloae produces the smallest flowers of the genus. Of the individuals that have been found, the largest flower clocked in at 3.83 inches (9.37 cm) in diameter. Needless to say, this was an exciting discovery and those responsible for it quickly set about observing the plant in detail. Cameras were set up to monitor flower development as well as to keep track of any animals that might pay it a visit. It turns out that, like its cousins, R. consueloae appears to be a specialist parasite on a group of vines in the genus Tetrastigma.

One of the unique characteristics of R. consueloae, other than its size, is the fact that its flowers don’t seem to produce any noticeable scent. This is a bit odd considering that its cousins are frequently referred to as “corpse flowers” thanks to the fact that they both look and smell like rotting meat. That is not to say that this species produces no scent at all. In fact, researchers noted that the fruits of R. consueloae smell a bit like coconut.

Its discoverers were quick to note that the discovery of such a strange parasitic plant in this particular stretch of forest is exciting because of the state of disrepair the forest is in. This region has suffered heavily from deforestation and fragmentation and it has long been thought that such specialized parasites like those in the genus Rafflesia could not persist after logging. As such, this discovery offers at least some hope that they may not be as sensitive as we once thought. Still, that does not mean that R. consueloae is by any means secure in its future.

To date, R. consueloae has only been found growing in two localities in Pantabangan, Phillippines. Though it is possible that more populations will be found growing elsewhere, its limited distribution nonetheless places it at high risk for extinction. Further habitat loss and the potential for anthropogenic forest fires are considerable threats to these plants and the hosts they simply can’t live without.

Despite plenty of observation, no one is quite sure how this species manages to reproduce successfully. Individual flowers are said to be either male or female but without a scent, its hard to say who or what pollinates them. Similarly, it still remains a mystery as to how R. consueloae (or any of its relatives for that matter) accomplish seed dispersal. Some small mammals were seen feeding on fruits but what happens after that is anyone’s guess. It seems like the various Rafflesiaceae still have many mysteries to be solved.

Photo Credit: [1]

Further Reading: [1]

 

Maxipiñon: One of the Rarest Pines in the World

Photo by Ruff tuff cream puff licensed under public domain

Photo by Ruff tuff cream puff licensed under public domain

The maxipiñon (Pinus maximartinezii) is one of the rarest pines on Earth. A native of southern Sierra Madre Occidental, Mexico, nearly all individuals of this species can be found scattered over an area that collectively spans only about 3 to 6 square miles (5 – 10 km²) in size. Needless to say, the maxipiñon teeters on the brink of extinction. As a result, a lot of effort has been put forward to better understand this species and to develop plans aimed at ensuring it is not lost forever.

The maxipiñon has only been known to science for a few decades. It was described back in 1964 after botanist Jerzy Rzedowski noted some exceptionally large pine seeds for sale at a local market. He named the species in honor of Maximino Martínez, who contributed greatly to our understanding of Mexican conifers. However, it was very obvious that the maxipiñon was well known among the residents of Zacatecas.

Pinus_maximartinezii_range_map_1.png

The reason for this are its seeds. The maxipiñon is said to produce the largest and most nutritious seeds of all the pines. As such, it is a staple of the regional diet. Conversations with local farmers suggest that it was much more common as recent as 60 years ago. Since then, its numbers have been greatly reduced. It soon became apparent that in order to save this species, we had to learn a lot more about what threatens its survival.

The most obvious place to start was recruitment. If any species is to survive, reproduction must outpace death. A survey of local markets revealed that a lot of maxipiñon seeds were being harvest from the wild. This would be fine if maxipiñon were widespread but this is not the case. Over-harvesting of seeds could spell disaster for a species with such small population sizes.

Indeed, surveys of wild maxipiñon revealed there to be only 2,000 to 2,500 mature individuals and almost no seedlings. However, mature trees do produce a considerable amount of cones. Therefore, the conclusion was made that seed harvesting may be the single largest threat to this tree. Subsequent research has suggested that seed harvests actually may not be the cause of its rarity. It turns out, maxipiñon population growth appears to be rather insensitive to the number of seeds produced each year. Instead, juvenile tree survival seems to form the biggest bottleneck to population growth.

Photo by Krzysztof Ziarnek, Kenraiz licensed under CC BY-SA 4.0

You see, this tree appears to be more limited by suitable germination sites than it does seed numbers. It doesn’t matter if thousands of seeds are produced if very few of them ever find a good spot to grow. Because of this, scientists feel that there are other more serious threats to the maxipiñon than seed harvesting. However, humans are still not off the hook. Other human activities proved to be far more damaging.

About 50 years ago, big changes were made to local farming practices. More and more land was being cleared for cattle grazing. Much of that clearing was done by purposefully setting fires. The bark of the maxipiñon is very thin, which makes it highly susceptible to fire. As fires burn through its habitat, many trees are killed. Those that survive must then contend with relentless overgrazing by cattle. If that wasn’t enough, the cleared land also becomes highly eroded, thus further reducing its suitability for maxipiñon regeneration. Taken together, these are the biggest threats to the ongoing survival of this pine. Its highly fragmented habitat no longer offers suitable sites for seedling growth and survival.

As with any species this rare, issues of genetic diversity also come into play. Though molecular analyses have shown that maxipiñon does not currently suffer from inbreeding, it has revealed some interesting data that give us hints into the deeper history of this species. Written in maxipiñon DNA is evidence of an extreme population bottleneck that occurred somewhere between 400 and 1000 years ago. It appears that this is not the first time this tree has undergone population decline.

There are a few ways in which these data can be interpreted. One is that the maxipiñon evolved relatively recently from a small number of unique and isolated individuals. Perhaps a hybridization event occurred between two closely related piñon species - the weeping piñon (Pinus pinceana) and Nelson piñon (Pinus nelsonii). Another possibility, which does not rule out hybridization, is that the maxipiñon may actually be the result of artificial selection by agriculturists of the region. Considering the value of its seeds today, it is not hard to imagine farmers selecting and breeding piñon for larger seeds. It goes without saying that these claims are largely unsubstantiated and would require much more evidence to say with any certainty, however, there is plenty of evidence that civilizations like the Mayans were conserving and propagation useful tree species much earlier than this.

Despite all we have learned about the maxipiñon over the last few decades, the fate of this tree is far from secure. Ex situ conservation efforts are well underway and you can now see maxipiñon specimens growing in arboreta and botanical gardens around the world. Seeds from these populations are being used for storage and to propagate more trees. Sadly, until something is done to protect the habitat on which it relies, there is no telling how long this species will last in the wild. This is why habitat conservation efforts are so important. Please support local land conservation efforts in your area because the maxipiñon is but one species facing the loss of its habitat.

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

Further Reading [1] [2] [3]

The Creeping Strawberry Pine

Photo by Tindo2 - Tim Rudman licensed under CC BY-NC 2.0

Photo by Tindo2 - Tim Rudman licensed under CC BY-NC 2.0

With its small, creeping habit and bright red, fleshy female cones, it is easy to see how Microcachrys tetragona earned its common name “creeping strawberry pine.” This miniature conifer is as adorable as it is interesting. With a fossil history that spans 66 million years of Earth’s history, it also has a lot to teach us about biogeography.

Today, the creeping strawberry pine can only be found growing naturally in western Tasmania. It is an alpine species, growing best in what is commonly referred to as alpine dwarf scrubland, above 1000 m (3280 ft) in elevation. Like the rest of the plants in such habitats, the creeping strawberry pine does not grow very tall at all. Instead, it creeps along the ground with its prostrate branches that barely extend more than 30 cm (0.9 ft) above the soil. This, of course, is likely an adaptation to its alpine environment. Plants that grow too tall frequently get knocked back by brutal winds and freezing temperatures among other things.

The creeping strawberry pine is not a member of the pine family (Pinaceae) but rather the podocarp family (Podocarpaceae). This family is interesting for a lot of reasons but one of the coolest is the fact that they are charismatic representatives of the so-called Antarctic flora. Along with a handful of other plant lineages, it is thought that Podocarpaceae arose during a time when most of the southern continents were combined into a supercontinent called Gondwana. Subsequent tectonic drift has seen the surviving members of this flora largely divided among the continents of the Southern Hemisphere. By combining current day distributions with fossil evidence, researchers are able to use families such as Podocarpaceae to tell a clearer picture of the history of life on Earth.

What is remarkable is that among the various podocarps, the genus Microcachrys produces pollen with a unique morphology. When researchers look at pollen under the microscope, whether extant or fossilized, they can say with certainty if it belongs to a Microcachrys or not. The picture we get from fossil evidence paints an interesting story for Microcachrys diversity compared to what we see today. It turns out, Microcachrys endemic status is a more recent occurrence.

This distinctive, small, trisaccate pollen grain is typical of what you find with Microcachrys whereas all other podocarps produce bisaccate pollen. J.I. Raine, D.C. Mildenhall, E.M. Kennedy (2011). New Zealand fossil spores and pollen: an illustrat…

This distinctive, small, trisaccate pollen grain is typical of what you find with Microcachrys whereas all other podocarps produce bisaccate pollen. J.I. Raine, D.C. Mildenhall, E.M. Kennedy (2011). New Zealand fossil spores and pollen: an illustrated catalogue. 4th edition. GNS Science miscellaneous series no. 4. http://data.gns.cri.nz/sporepollen/index.htm

The creeping strawberry pine is what we call a paleoendemic, meaning it belongs to a lineage that was once far more widespread but today exists in a relatively small geographic location. Fossilized pollen from Microcachrys has been found across the Southern Hemisphere, from South America, India, southern Africa, and even Antarctica. It would appear that as the continents continued to separate and environmental conditions changed, the mountains of Tasmania offered a final refuge for the sole remaining species in this lineage.

Another reason this tiny conifer is so charming are its fruit-like female cones. As they mature, the scales around the cone swell and become fleshy. Over time, they start to resemble a strawberry more than anything a gymnosperm would produce. This is yet another case of convergent evolution on a seed dispersal mechanism among a gymnosperm lineage. Birds are thought to be the main seed dispersers of the creeping strawberry pine and those bright red cones certainly have what it takes to catch the eye of a hungry bird. It must be working well for it too. Despite how narrow its range is from a global perspective, the creeping strawberry pine is said to be locally abundant and does not face the same conservation issues that many other members of its family currently face. Also, its unique appearance has made it something of a horticultural curiosity, especially among those who like to dabble in rock gardening.

Mature female cones look more like angiosperm fruit than a conifer cone. Photo by Mnyberg licensed under CC BY-SA 4.0

Mature female cones look more like angiosperm fruit than a conifer cone. Photo by Mnyberg licensed under CC BY-SA 4.0

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

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

The Golden Fuchsia: A Case Study in Why Living Collections Matter

Photo by FarOutFlora licensed under CC BY-NC-ND 2.0

Photo by FarOutFlora licensed under CC BY-NC-ND 2.0

The golden Fuchsia (Deppea splendens) is a real show stopper. It is impossible to miss this plant when it is in full bloom. Amazingly, if it were not for the actions of one person, this small tree may have disappeared without anyone ever knowing it existed in the first place. The golden Fuchsia is yet another plant that currently exists only in cultivation.

The story of the golden Fuchsia starts in the early 1970’s. During a trek through the mountains of southern Mexico, Dr. Dennis Breedlove, then the curator of botany for the California Academy of Sciences, stumbled across a peculiar looking shrub growing in a steep canyon. It stood out against the backdrop of Mexican oaks, pines, and magnolias. Standing at about 15 to 20 feet tall and adorned with brightly colored, pendulous inflorescences, it was clear that this species was something special indeed.

Photo by FarOutFlora licensed under CC BY-NC-ND 2.0

Photo by FarOutFlora licensed under CC BY-NC-ND 2.0

A subsequent expedition to Chiapas in the early 1980’s was aimed at collecting seeds of this wonderful plant. It turned out to be relatively easy to germinate and grow, provided it didn’t experience any hard frost events. Plants were distributed among botanical gardens and nurseries and it appeared that the golden Fuchsia was quickly becoming something of a horticultural treasure. Despite all of the attention it was paid, the golden Fuchsia was only properly described in 1987.

Sadly, around the same time that botanists got around to formally naming the plant, tragedy struck. During yet another trip to Chiapas, Dr. Breedlove discovered that the cloud forest that once supported the only known population of golden Fuchsia had been clear cut for farming. Nothing remained but pasture grasses. No other wild populations of the golden Fuchsia have ever been found.

Photo by Stickpen licensed under public domain

Photo by Stickpen licensed under public domain

If it was not for those original seed collections, this plant would have gone completely extinct. It owes its very existence to the botanical gardens and horticulturists that have propagated it over the last 30+ years. All of the plants you will encounter today are descendants of that original collection.

The role of ex situ living collections play in the conservation of species is invaluable. The golden Fuchsia is yet another stark reminder of this. If it were not for people like Dr. Breedlove and all of the others who have dedicated time and space to growing the golden Fuchsia, this species would have only been known as a curious herbarium specimen. The most alarming part about all of this is that as some botanical gardens continue to devalue living collections in favor of cheap landscaping and event hosting, living collections are getting pushed to the side, neglected, or even worse, destroyed. We must remember that living collections are a major piece of the conservation puzzle and their importance only grows as we lose more and more wild spaces to human expansion.

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

Further Reading: [1] [2]

A New Species of Waterfall Specialist Has Been Discovered In Africa

A. habit, whole plant, in fruit, showing the flat root, a pillar-like ‘haptera’, and a shoot with three inflorescences, B. detail of shoot with three branches, C. view of upper surface of a flattened root, with six short, erect shoots, each with 1–2…

A. habit, whole plant, in fruit, showing the flat root, a pillar-like ‘haptera’, and a shoot with three inflorescences, B. detail of shoot with three branches, C. view of upper surface of a flattened root, with six short, erect shoots, each with 1–2 1-flowered inflorescences emerging from spathellum remains, D. side view of plant showing, on the lower surface of the flattened root, the pillar-like haptera, branched at base; upper surface of root with spathellum-sheathed inflorescence base, E. plant attached to rock by weft of thread-like root hairs (indicated with arrow) from base of pillar-like haptera; upper surface of flattened root with two shoots, F. side view of flower showing one of two tepals in full frontal view, G. as F. with tepal removed, exposing the gynoecium with, to left, the arched-over androecium, H. side view of flower with androecium in centre, two tepals flanking the gynoecium, I. androecium (leftmost of three anthers missing), J. transverse section of andropodium, K. view of gynoecium from above showing funneliform style-stigma base, L. fruit, dehisced, M. transverse section of bilocular fruit, showing septum and placentae, N. placentae with seeds, divided by septum, O. seeds, P. seed with mucilage outer layer. Drawn by Andrew Brown from Lebbie A2721 [SOURCE]

At first glance, this odd plant doesn’t look very special. However, it is the first new member of the family Podostemaceae to be found in Africa in over 30 years. It has been given the name Lebbiea grandiflora and it was discovered during a survey to assess the impacts of a proposed hydroelectric dam. By examining the specimen, Kew botanists quickly realized this plant was unique. Sadly, if all goes according to plan, this species may not be long for this world unless something is done to preserve it.

Members of the family Podostemaceae are strange plants. Despite how delicate they look, these plants specialize in growing submersed on rocks in waterfalls, rapids, and other fast flowing bodies of water. They are generally small plants, though some species can grow to lengths of 3 ft. (1 m) or more. The best generalization one can make about this group is that they like clean, fast-flowing water with plenty of available rock surfaces to grow on.

Lebbiea grandiflora certainly fits this description. It is native to a small portion of Sierra Leone and Guinea where it grows on slick rock surfaces only during the wet season. As the dry season approaches and the rivers shrink in size, L. grandiflora quickly sets seed and dies.

As mentioned, the area in which this plant was discovered is slated for the construction of a large hydroelectric dam. The building of this dam will most certainly destroy the entire population of this plant. As soon as water slows, becomes more turbid, and sediments build up, most Podostemaceae simply disappear. Unfortunately, I appears this plant was in trouble even before the dam came into the picture.

As mentioned, Podostemaceae need clean rock surfaces on which to germinate and grow. Without them, the seedlings simply can’t get established. Mining operations further upstream of the Sewa Rapids have been dumping mass quantities of sediment into the river for years. All of this sediment eventually makes it down into L. grandiflora territory and chokes out available germination sites.

Alarmed at the likely extinction of this new species, the Kew team wanted to try and find other populations of L. grandiflora. Amazingly, one other population was found growing in a river near Koukoutamba, Guinea. Sadly, the discovery of this additional population is bitter sweet as the World Bank is apparently backing another hydro-electric dam project on that river as well.

The only hope for the continuation of this species currently will be to (hopefully) find more populations and collect seed to establish ex situ populations both in other rivers as well as in captivity if possible. To date, no successful purposeful seeding of any Podostemaceae has been reported (if you know of any, please speak up!). Currently L. grandiflora has been given “Critically Endangered” status by the IUCN and the botanists responsible for its discovery hope that, coupled with the publication of this new species description, more can be done to protect this small rheophytic herb.

Photo Credit: [1] [2]

Further Reading: [1]

The Flora of Antarctica: Life on a Frozen Continent

Photo by Carloszelayeta licensed under the GNU Free Documentation License.

Photo by Carloszelayeta licensed under the GNU Free Documentation License.

Antarctica - the frozen continent. It is hard to think of a place on Earth that is less hospitable to life. Yet life does exist here and some of it is botanical. Though few in number, Anarctica’s diminutive flora is able to eke out an existence wherever the right conditions present themselves. It goes without saying that these plants are some of the hardiest around.

It is strange to think of Antarctica as having any flora at all. How many descriptions of plant families and genera say something to the effect of “found on nearly every continent except for Antarctica.” It didn’t always used to be this way though. Antarctica was once home to a diverse floral assemblage that rivaled anything we see in the tropics today. Millions upon millions of years of continental drift has seen this once lush landmass positioned squarely at Earth’s southern pole.

Antarctica_6400px_from_Blue_Marble.jpg

Situated that far south, Antarctica has long since become a frozen wasteland of sorts. The landscape is essentially a desert. Instead of no precipitation, however, most water in this neck of the woods is completely locked up in ice for most of the year. This is one reason why plants have had such a hard time making a living there. That is not to say that some plants haven’t made it. In fact, a handful of species thrive under these conditions.

When anyone goes looking for plants in Antarctica, they must do so wherever conditions ease up enough for part of the year to allow terrestrial life to exist. In the case of this frozen continent, this means hanging out along the coast or one of handful of islands situated just off of the mainland. Here, enough land thaws during the brief summer months to allow a few plant species to take root and grow.

Antarctic hair grass (Deschamsia antarctica). Photo by Lomvi2 licensed under CC BY-SA 3.0

Antarctic hair grass (Deschamsia antarctica). Photo by Lomvi2 licensed under CC BY-SA 3.0

The flora of Antarctica proper consists of 2 flowering plant species, about 100 species of mosses, and roughly 30 species of liverwort. The largest of these are the flowering plants - a grass known as Antarctic hair grass (Deschamsia antarctica), and member of the pink family with a cushion-like growth habit called Antarctic pearlwort (Colobanthus quitensis). Whereas the hair grass benefits from being wind pollinated, the Antarctic pearlwort has had to get creative with its reproductive needs. Instead of relying on pollinators, which simply aren’t present in any abundance on Antarctica, it appears that the pearlwort has shifted over to being entirely self-pollinated. This seems to work for it because if the mother plant is capable of living on Antarctica, so too will its clonal offspring.

By far the dominant plant life on the continent are the mosses. With 100 species known to live on Antarctica, it is hard to make generalizations about their habits other than to say they are pretty tough plants. Most live out their lives among the saturated rocks of the intertidal zones. What we can say about these mosses is that they support a bewildering array of microbial life, from fungi and lichens to protists and tardigrades. Even in this frozen corner of the world, plants form the foundation for all other forms of life.

Photo by Liam Quinn licensed under CC BY-SA 2.0

Photo by Liam Quinn licensed under CC BY-SA 2.0

Antarctic pearlwort (Colobanthus quitensis). Photo by Patricio Novoa Quezada licensed under CC BY 2.0

Antarctic pearlwort (Colobanthus quitensis). Photo by Patricio Novoa Quezada licensed under CC BY 2.0

The coastal plant communities of Antarctica represent hotbeds of biodiversity for this depauperate continent. They reach their highest densities on the Antarctic Peninsula as well as on coastal islands such as south Orkney Islands and the South Shetland Islands. Here, conditions are just mild enough among the various rocky crevices for germination and growth to occur. Still, life on Antarctica is no cake walk. A short growing season, punishing waves, blistering winds, and trampling by penguins and seals present quite a challenge to Antarctica’s botanical denizens. They are able to live here despite these challenges.

Photo by Gilad Rom licensed under CC BY-NC 2.0

Photo by Gilad Rom licensed under CC BY-NC 2.0

Still, humans take their toll. The Antarctic Peninsula is experiencing some of the most rapid warming on the planet over the last century. As this region grows warmer and drier each year, plants are responding accordingly. Antarctic mosses along the peninsula are increasingly showing signs of stress. They are starting to prioritize the production of protective pigments in their tissues over growth and reproduction. Moreover, new species of moss are starting to take over. Rapid warming and drying of the Antarctic Peninsula appears to be favoring species that are more desiccation tolerant at the expense of the continents endemic moss species.

Changes in the structure and composition of Antarctica’s moss beds is far from being a scientific curiosity for only bryologists to ponder. It is a symptom of greater changes to come.

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

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

The Curious Case of the Yellowwood Tree

Photo by Plant Image Library licensed under CC BY-SA 2.0

Photo by Plant Image Library licensed under CC BY-SA 2.0

The immense beauty and grace of the yellowwood (Cladrastis kentukea) is inversely proportional to its abundance. This unique legume is endemic to the eastern United States and enjoys a strangely patchy distribution. Its ability to perform well when planted far outside of its natural range only deepens the mystery of the yellowwood.

The natural range of the yellowwood leaves a lot of room for speculation. It hits its highest abundances in the Appalachian and Ozark highlands where it tends to grow on shaded slopes in calcareous soils. Scattered populations can be found as far west as Oklahoma and as far north as southern Indiana but nowhere is this tree considered a common component of the flora.

Cladrastis_kentukea_range_map_1.png

Though the nature of its oddball distribution pattern iscurious to say the least, it is likely that its current status is the result of repeated glaciation events and a dash of stochasticity. The presence of multiple Cladrastis species in China and Japan and only one here in North America is a pattern shared by multiple taxa that once grew throughout each continent. A combination of geography, topography, and repeated glaciation events has since fragmented the ranges of many genera and perhaps Cladrastis is yet another example.

The fact that yellowwood seems to perform great as a specimen tree well outside of its natural range says to me that this species was probably once far more wide spread in North America than it is today. It may have been pushed south by the ebb and flow of the Laurentide Ice Sheet and, due to the stochastic nuances of seed dispersal, never had a chance to recolonize the ground it had lost. Again, this is all open to speculation as this point.

Despite being a member of the pea family, yellowwood is not a nitrogen fixer. It does not produce nodules on its roots that house rhizobium. As such, this species may be more restricted by soil type than other legumes. Perhaps its inability to fix nitrogen is part of the reason it tends to favor richer soils. It may also have played a part in its failure to recolonize land scraped clean by the glaciers.

Yellowwood's rarity in nature only makes finding this tree all the more special. It truly is a sight to behold. It isn't a large tree by any standards but what it lacks in height it makes up for in looks. Its multi-branched trunk exhibits smooth, gray bark reminiscent of beech trees. Each limb is decked out in large, compound leaves that turn bright yellow in autumn.

Photo by Elektryczne jabłko licensed under CC BY-SA 4.0

Photo by Elektryczne jabłko licensed under CC BY-SA 4.0

When mature, which can take upwards of ten years, yellowwood produces copious amounts of pendulous inflorescences. Each inflorescence sports bright white flowers with a dash of yellow on the petals. In some instances, even pink flowers are produced! It doesn't appear that any formal pollination work has been done on this tree but surely bees and butterflies alike visit the blooms. The name yellowwood comes from the yellow coloration of its heartwood, which has been used to make furniture and gunstocks in the past.

Whether growing in the forest or in your landscape, yellowwood is one of the more stunning trees you will find in eastern North America. Its peculiar natural history only lends to its allure.

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

Further Reading: [1] [2]

Saving One of North America's Rarest Shrubs

Photo by Stan Shebs licensed under CC BY-SA 3.0

Photo by Stan Shebs licensed under CC BY-SA 3.0

The chance to save a species from certain extinction cannot be wasted. When the opportunity presents itself, I believe it is our duty to do so. Back in 2010, such an opportunity presented itself to the state of California and what follows is a heroic demonstration of the lengths dedicated individuals will go to protect biodiversity. Thought to be extinct for 60 years, the Franciscan manzanita (Arctostaphylos franciscana) has been given a second chance at life on this planet.

California is known the world over for its staggering biodiversity. Thanks to a multitude of factors that include wide variations in soil and climate types, California boasts an amazing variety of plant life. Some of the most Californian of these plants belong to a group of shrubs and trees collectively referred to as 'manzanitas.' These plants are members of the genus Arctostaphylos, which hails from the family Ericaceae, and sport wonderful red bark, small green leaves, and lovely bell-shaped flowers. Of the approximately 105 species, subspecies, and varieties of manzanita known to science, 95 of them can be found growing in California.

It has been suggested that manzanitas as a whole are a relatively recent taxon, having arisen sometime during the Middle Miocene. This fact complicates their taxonomy a bit because such a rapid radiation has led manzanita authorities to recognize a multitude of subspecies and varieties. In California, there are also many endemic species that owe their existence in part to the state's complicated geologic history. Some of these manzanitas are exceedingly rare, having only been found growing in one or a few locations. Sadly, untold species were probably lost as California was settled and human development cleared the land. 

Such was the case for the Franciscan manzanita. Its discovery dates back to the late 1800's. California botanist and manzanita expert, Alice Eastwood, originally collected this plant on serpentine soils around the San Francisco Bay Area. In the years following, the growing human population began putting lots of pressure on the surrounding landscape.

Photo by Daderot (public domain)

Photo by Daderot (public domain)

Botanists like Eastwood recognized this and went to work doing what they could to save specimens from the onslaught of bulldozers. Luckily, the Franciscan manzanita was one such species. A few individuals were dug up, rooted, and their progeny were distributed to various botanical gardens. By the 1940's, the last known wild population of Franciscan manzanita were torn up and replaced by the unending tide of human expansion into the Bay Area.

It was apparent that the Franciscan manzanita was gone for good. Nothing was left of its original populations outside of botanical gardens. It was officially declared extinct in the wild. Decades went by without much thought for this plant outside of a few botanical circles. All of that changed in 2009.

It was in 2009 when a project began to replace a stretch of roadway called Doyle Drive. It was a massive project and a lot of effort was invested to remove the resident vegetation from the site before work could start in earnest. Native vegetation was salvaged to be used in restoration projects but most of the clearing involved the removal of aggressive roadside trees. A chipper was brought in to turn the trees into wood chips. Thanks to a bit of serendipity, a single area of vegetation bounded on all sides by busy highway was spared from wood chip piles. Apparently the only reason for this was because a patrol car had been parked there during the chipping operation.

Cleared of tall, weedy trees, this small island of vegetation had become visible by road for the first time in decades. That fall, a botanist by the name of Daniel Gluesenkamp was driving by the construction site when he noticed an odd looking shrub growing there. Luckily, he knew enough about manzanitas to know something was different about this shrub. Returning to the site with fellow botanists, Gluesenkamp and others confirmed that this odd shrubby manzanita was in fact the sole surviving wild Franciscan manzanita. Needless to say, this caused a bit of a stir among conservationists.

median arc.JPG

The shrub had obviously been growing in that little island of serpentine soils for quite some time. The surrounding vegetation had effectively concealed its presence from the hustle and bustle of commuters that crisscross this section of on and off ramps every day. Oddly enough, this single plant likely owes its entire existence to the disturbance that created the highway in the first place. Manzanitas lay down a persistent seed bank year after year and those seeds can remain dormant until disturbance, usually fire but in this case road construction, awakens them from their slumber. It is likely that road crews had originally disturbed the serpentine soils just enough that this single Franciscan manzanita was able to germinate and survive.

The rediscovery of the last wild Franciscan manzanita was bitter sweet. On the one hand, a species thought extinct for 60 years had been rediscovered. On the other hand, this single individual was extremely stressed by years of noxious car exhaust and now, the sudden influx of sunlight due to the removal of the trees that once sheltered it. What's more, this small island of vegetation was doomed to destruction due to current highway construction. It quickly became apparent that if this plant had any chance of survival, something drastic had to be done.

Many possible rescue scenarios were considered, from cloning the plant to moving bits of it into botanical gardens. In the end, the most heroic option was decided on - this single Franciscan manzanita was going to be relocated to a managed natural area with a similar soil composition and microclimate.

Moving an established shrub is not easy, especially when that particular individual is already stressed to the max. As such, numerous safeguards were enacted to preserve the genetic legacy of this remaining wild individual just in case it did not survive the ordeal. Stem cuttings were taken so that they could be rooted and cloned in a lab. Rooted branches were cut and taken to greenhouses to be grown up to self-sustaining individuals. Numerous seeds were collected from the surprising amount of ripe fruits present on the shrub that year. Finally, soil containing years of this Franciscan manzanita's seedbank as well as the microbial community associated with the roots, were collected and stored to help in future reintroduction efforts.

A fran rescue.JPG

Finally, the day came when the plant was to be dug up and moved. Trenches were dug around the root mass and a dozen metal pipes were driven into the soil 2 feet below the plant so that the shrub could safely be separated from the soil in which it had been growing all its life. These pipes were then bolted to I-beams and a crane was used to hoist the manzanita up and out of the precarious spot that nurtured it in secret for all those years.

Upon arriving at its new home, experts left nothing to chance. The shrub was monitored daily for the first ten days of its arrival followed by continued weekly visits after that. As anyone that gardens knows, new plantings must be babied a bit before they become established.  For over a year, this single shrub was sheltered from direct sun, pruned of any dead and sickly branches, and carefully weeded to minimize competition. Amazingly, thanks to the coordinated effort of conservationists, the state of California, and road crews, this single individual lives on in the wild.

Of course, one single individual is not enough to save this species from extinction. At current, cuttings, and seeds provide a great starting place for further reintroduction efforts. Similarly, and most importantly, a bit of foresight on the part of a handful of dedicated botanists nearly a century ago means that the presence of several unique genetic lines of this species living in botanical gardens means that at least some genetic variability can be introduced into the restoration efforts of the Franciscan manzanita.

In an ideal world, conservation would never have to start with a single remaining individual. As we all know, however, this is not an ideal world. Still, this story provides us with inspiration and a sense of hope that if we can work together, amazing things can be done to preserve and restore at least some of what has been lost. The Franciscan manzanita is but one species that desperately needs our help an attention. It is a poignant reminder to never give up and to keep working hard on protecting and restoring biodiversity.

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

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

 

An Endangered Iris With An Intriguing Pollination Syndrome

iris1.JPG

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. 

Photo by Dr. Avishai Teicher Pikiwiki Israel licensed under CC BY 2.5

Photo by Dr. Avishai Teicher Pikiwiki Israel licensed under CC BY 2.5

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. Photo by Gideon Pisanty (Gidip) גדעון פיזנטי • CC BY 3.0

A Eucerine bee visiting a nectar source. Photo by Gideon Pisanty (Gidip) גדעון פיזנטי • CC BY 3.0

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.

Photo by Dr. Avishai Teicher Pikiwiki Israel licensed under CC BY 2.5

Photo by Dr. Avishai Teicher Pikiwiki Israel licensed under CC BY 2.5

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]

 

Saving Bornean Peatlands is a Must For Conservation

Photo by Dukeabruzzi licensed under CC BY-SA 4.0

Photo by Dukeabruzzi licensed under CC BY-SA 4.0

The leading cause of extinction on this planet is loss of habitat. As an ecologist, it pains me to see how frequently this gets ignored. Plants, animals, fungi - literally every organism on this planet needs a place to live. Without habitat, we are forced to pack our flora and fauna into tiny collections in zoos and botanical gardens, completely disembodied from the environment that shaped them into what we know and love today. That’s not to say that zoos and botanical gardens don’t play critically important roles in conservation, however, if we are going to stave off total ecological meltdown, we must also be setting aside swaths of wild lands.

There is no way around it. We cannot have our cake and eat it too. Land conservation must be a priority both at the local and the global scale. Wild spaces support life. They buffer life from storms and minimize the impacts of deadly diseases. Healthy habitats filter the water we drink and, for many people around the globe, provide much of the food we eat. Every one of us can think back to our childhood and remember a favorite stretch of stream, meadow, or forest that has since been gobbled up by a housing development. For me it was a forested stream where I learned to love the natural world. I would spend hours playing in the creek, climbing trees, and capturing bugs to show my parents. Since that time, someone leveled the forest, built a house, and planted a lawn. With that patch of forest went all of the insects, birds, and wildflowers it once supported.

Scenarios like this play out all too often and sadly on a much larger scale than a backyard. Globally, forests have taken the brunt of human development. It is hard to get a sense of the scope of deforestation on a global scale, but the undisputed leaders in deforestation are Brazil and Indonesia. Though the Amazon gets a lot of press, few may truly grasp the gravity of the situation playing out in Southeast Asia.

Deforestation is a clear and present threat throughout tropical Asia. This region is growing both in its economy and population by about 6% every year and this growth has come at great cost to the environment. Indonesia (alongside Brazil) accounts for 55% of the world’s deforestation rates. This is a gut-wrenching statistic because Indonesia alone is home to the most extensive area of intact rainforest in all of Asia. So far, nearly a quarter of Indonesia’s forests have been cleared. It was estimated that by 2010, 2.3 million hectares of peatland forests had been felled and this number shows little signs of slowing. Experts believe that if these rates continue, this area could lose the remainder of its forests by 2056.

Consider the fact that Southeast Asia contains 6 of the world’s 25 biodiversity hotspots and you can begin to imagine the devastating blow that the levelling of these forests can have. Much of this deforestation is done in the name of agriculture, and of that, palm oil and rubber take the cake. Southeast Asia is responsible for producing 86% of the world’s palm oil and 87% of the world’s natural rubber. What’s more, the companies responsible for these plantations are ranked among some of the least sustainable in the world.

Borneo is home to a bewildering array of life. Researchers working there are constantly finding and describing new species, many of which are found nowhere else in the world. Of the roughly 15,000 plant species known from Borneo, botanists estimate that nearly 5,000 (~34%) of them are endemic. This includes some of the more charismatic plant species such as the beloved carnivorous pitcher plants in the genus Nepenthes. Of these, 50 species have been found growing in Borneo, many of which are only known from single mountain tops.

It has been said that nowhere else in the world has the diversity of orchid species found in Borneo. To date, roughly 3,000 species have been described but many, many more await discovery. For example, since 2007, 51 new species of orchid have been found. Borneo is also home to the largest flower in the world, Rafflesia arnoldii. It, along with its relatives, are parasites, living their entire lives inside of tropical vines. These amazing plants only ever emerge when it is time to flower and flower they do! Their superficial resemblance to a rotting carcass goes much deeper than looks alone. These flowers emit a fetid odor that is proportional to their size, earning them the name “carrion flowers.”

Rafflesia arnoldii in all of its glory. Photo by SofianRafflesia licensed under CC BY-SA 4.0

Rafflesia arnoldii in all of its glory. Photo by SofianRafflesia licensed under CC BY-SA 4.0

Photo by Orchi licensed under CC BY-SA 3.0

Photo by Orchi licensed under CC BY-SA 3.0

If deforestation wasn’t enough of a threat to these botanical treasures, poachers are having considerable impacts on Bornean botany. The illegal wildlife trade throughout southeast Asia gets a lot of media attention and rightfully so. At the same time, however, the illegal trade of ornamental and medicinal plants has gone largely unnoticed. Much of this is fueled by demands in China and Vietnam for plants considered medicinally valuable. At this point in time, we simply don’t know the extent to which poaching is harming plant populations. One survey found 347 different orchid species were being traded illegally across borders, many of which were considered threatened or endangered. Ever-shrinking forested areas only exacerbate the issue of plant poaching. It is the law of diminishing returns time and time again.

Photo by Orchi licensed under CC BY-SA 3.0

Photo by Orchi licensed under CC BY-SA 3.0

But to lump all Bornean forests under the general label of “rainforest” is a bit misleading. Borneo has multitude of forest types and one of the most globally important of these are the peatland forests. Peatlands are vital areas of carbon storage for this planet because they are the result of a lack of decay. Whereas leaves and twigs quickly breakdown in most rainforest situations, plant debris never quite makes it that far in a peatland. Plant materials that fall into a peatland stick around and build up over hundreds and thousands of years. As such, an extremely thick layer of peat is formed. In some areas, this layer can be as much as 20 meters deep! All the carbon tied up in the undecayed plant matter is carbon that isn’t finding its way back into our atmosphere.

Sadly, tropical peatlands like those found in Borneo are facing a multitude of threats. In Indonesia alone, draining, burning, and farming (especially for palm oil) have led to the destruction of 1 million hectares (20%) of peatland habitat in only a single decade. The fires themselves are especially worrisome. For instance, it was estimated that fires set between 1997-1998 and 2002-2003 in order to clear the land for palm oil plantations released 200 million to 1 billion tonnes of carbon into our atmosphere. Considering that 60% of the world’s tropical peatlands are found in the Indo-Malayan region, these numbers are troubling.

The peatlands of Borneo are totally unlike peatlands elsewhere in the world. Instead of mosses, gramminoids, and shrubs, these tropical peatlands are covered in forests. Massive dipterocarp trees dominate the landscape, growing on a spongey mat of peat. What’s more, no water flows into these habitats. They are fed entirely by rain. The spongey nature of the peat mat holds onto water well into the dry season, providing clean, filtered water where it otherwise wouldn’t be available.

Photo by JeremiahsCPs licensed under CC BY-SA 3.0

Photo by JeremiahsCPs licensed under CC BY-SA 3.0

This lack of decay coupled with their extremely acidic nature and near complete saturation makes peat lands difficult places for survival. Still, life has found a way, and Borneo’s peatlands are home to a staggering diversity of plant life. They are so diverse, in fact, that when I asked Dr. Craig Costion, a plant conservation officer for the Rainforest Trust, for something approaching a plant list for an area of peatland known as Rungan River region, he replied:

“Certainly not nor would there ever be one in the conceivable future given the sheer size of the property and the level of diversity in Borneo. There can be as many as a 100 species per acre of trees in Borneo... Certainly a high percentage of the species would only be able to be assigned to a genus then sit in an herbarium for decades until someone describes them.”

And that is quite remarkable when you think about it. When you consider that the Rungan River property is approximately 385,000 acres, the number of plant species to consider quickly becomes overwhelming. To put that in perspective, there are only about 500 tree species native to the whole of Europe! And that’s just considering the trees. Borneo’s peatlands are home to myriad plant species from liverworts, mosses, and ferns, to countless flowering plants like orchids and others. We simply do not know what kind of diversity places like Borneo hold. One could easily spend a week in a place like the Rungan River and walk away with dozens of plant species completely new to science. Losing a tract of forest in such a biodiverse region is a huge blow to global biodiversity.

Nepenthes ampullaria relies on decaying plant material within its pitcher for its nutrient needs. Photo by en:User:NepGrower licensed under Public Domain

Nepenthes ampullaria relies on decaying plant material within its pitcher for its nutrient needs. Photo by en:User:NepGrower licensed under Public Domain

Also, consider that all this plant diversity is supporting even more animal diversity. For instance, the high diversity of fruit trees in this region support a population of over 2,000 Bornean orangutans. That is nearly 4% of the entire global population of these great apes. They aren’t alone either, the forested peatlands of Borneo are home to species such as the critically endangered Bornean white-bearded gibbon, the proboscis monkey, the rare flat-headed cat, and the oddly named otter civet. All these animals and more rely on the habitat provided by these forests. Without forests, these animals are no more.

The flat-headed cat, an endemic of Borneo. Photo by Jim Sanderson licensed under CC BY-SA 3.0

The flat-headed cat, an endemic of Borneo. Photo by Jim Sanderson licensed under CC BY-SA 3.0

At this point, many of you may be feeling quite depressed. I know how easy it is to feel like there is nothing you can do to help. Well, what if I told you that there is something you can do right now to save a 385,000 acre chunk of peatland rainforest? That’s right, by heading over to the Rainforest Trust’s website (https://www.rainforesttrust.org/project/saving-stronghold-critically-endangered-bornean-orangutan/) you can donate to their campaign to buy up and protect the Rungan River forest tract.

Click on the logo to learn more!

Click on the logo to learn more!

By donating to the Rainforest Trust, you are doing your part in protecting biodiversity in one of the most biodiverse regions in the world. What’s more, you can rest assured that your money is being used effectively. The Rainforest Trust consistently ranks as one of the top environmental protection charities in the world. Over their nearly three decades of operation, the Rainforest Trust has protected more than 15.7 million acres of land in over 20 countries. Like I said in the beginning, habitat loss is the leading cause of extinction on this planet. Without habitat, we have nothing. Plants are that habitat and by supporting organizations such as the Rainforest Trust, you are doing your part to fight the biggest threats our planet faces. 

Further Reading: [1] [2] [3] [4] [5] [6] [7] [8] [9] [10]

Photo Credits: [1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11]

The Traveler's Palm

© CEphoto, Uwe Aranas licensed under CC BY-SA 3.0

© CEphoto, Uwe Aranas licensed under CC BY-SA 3.0

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 Madagascan 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.

Photo by H. Zell licensed under CC BY-SA 3.0

Photo by H. Zell licensed under CC BY-SA 3.0

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 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.

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.

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 muzzles 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 as well. 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.

Photo by Jeffdelonge licensed under CC BY-SA 3.0

Photo by Jeffdelonge licensed under CC BY-SA 3.0

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]

 

The Grasstree of Southwestern Australia

Taken by John O'Neill licensed under CC BY-SA 3.0

Taken by John O'Neill licensed under CC BY-SA 3.0

Southwestern Australia is home to a wonderful and unique flora. A combination of highly diverse, nutrient-poor soil types, bush fires, and lots of time have led to amazing adaptive radiations, the result of which are myriad plant species found nowhere else in the world. One of the most incredible members of southwestern Australia's flora is the grassplant (Kingia australis). Like all plants of this region, it is one hardy species.

The taxonomic history of the grassplant has been a bit muddled. As its common name suggests, it was once thought to be a type of grasstree (genus Xanthorrhoea), however, its resemblance to this group is entirely superficial. It has since been placed in the family Dasypogonaceae. Along with three other genera, this entire family is endemic to Australia. Growing in southwestern Australia presents lots of challenges such as obtaining enough water and nutrients to survive and for the grassplant, these have been overcome in some fascinating ways.

The way in which the grassplant manages this is incredible. Its trunk is not really a true trunk but rather a dense cluster of old leaf bases. Within this pseudotrunk, the grassplant grows a series of fine roots. Research has shown this to be an adaptation to life in a harsh climate. Because water can be scarce and nutrients are in short supply, the grassplant doesn't take any chances. Water hitting the trunk is rapidly absorbed by these roots as are any nutrients that come in the form of things like bird droppings.

Photo by Casliber licensed under CC BY-SA 3.0

Photo by Casliber licensed under CC BY-SA 3.0

Coupled with its underground roots, the grassplant is able to eek out a living in this dry and impoverished landscape. That being said, its life is spent in the slow lane. Plants are very slow growing and estimates place some of the larger individuals at over 600 years in age. Its amazing how some of the harshest environments can produce some of the longest lived organisms.

As you can probably imagine, reproduction in this species can also be a bit of a challenge. Every so often, flower clusters are produced atop long, curved stems. Their production is stimulated by fire but even then, with nutrients in poor supply, it is not a frequent event. Some plants have been growing for over 200 years without ever producing flowers. This lifestyle makes the grassplant sensitive to disturbance. Recruitment is limited, even in good flowering years and plants take a long time to mature. That is why conservation of their habitat is of utmost importance.

Photo Credits: [1] [2]

Further Reading: [1] [2]

Begonia's Hawaiian Cousin

Photo by Forest and Kim Starr licensed under CC BY 2.0

Photo by Forest and Kim Starr licensed under CC BY 2.0

Begoniaceae is a strange family. It consists of two genera - Begonia, which comprises roughly 1,400 species, and Hillebrandia, which consists of a single species endemic to Hawai'i (Symbegonia has since been placed back into Begonia). Although I adore the entire family, its that single genus that is the focus of our attention today. Far from being a strange one-off, Hillebrandia has a fascinating evolutionary history.

The sole species, Hillebrandia sandwicensis, is the only member of the family native to Hawai'i. It differs from the genus Begonia in characters such as its petals, which are more numerous and more differentiated, its ovaries, which do not completely close, as well as various morphological characteristics of its fruit and pollen, which I won't go into here. It occurs naturally only on the islands of Kauai, Maui, and Molokai where it inhabits wet ravines in montane rainforest zones. Nowhere is this species considered abundant. 

Since its discovery in 1866, H. sandwicensis has been the object of much curiosity. Where did it originate? How old of a species is it? How did it get to Hawai'i? Thanks to some molecular work, a few of these questions are becoming a bit more clear. For starters, we can now confidently say that Hillebrandia is a sister lineage to all other Begonias. This in turn has provided a crucial step in our understanding of its biogeography.

Photo by John Game licensed under CC BY 2.0

Photo by John Game licensed under CC BY 2.0

Molecular dating techniques place the genus Hillebrandia at about 51–65 million years old, much older than any of the Hawaiian islands. As such, it is likely that this lineage is not the results of an adaptive radiation like we see in most of the archipelago's flora and fauna. Instead, it is now believed that H. sandwicensis is the only known relict species in Hawaiian flora. In other words, the ancestor of H. sandwicensis did not arrive at Hawai'i and then evolve into the species we know today. Instead, it is more likely that the lineage arose elsewhere and then, through a random long-distance seed dispersal event, made it to Hawai'i's oldest islands some 30 million years ago and has been island hopping to younger islands ever since. 

Although its recent history and geographic origins are still open to much speculation, the story of this unique genus has gotten a bit clearer. Its status as Hawai'i's only known relict plant species is quite exciting to say the least. What we can say for sure is that its history was likely full of serendipity that should be celebrated each time someone has an encounter with this lovely Hawaiian plant.

Photo Credits: [1] [2]

Further Reading: [1]