A New Species of Waterfall Specialist Has Been Discovered In Africa

Lebbiea grandiflora Oct2018.JPG

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.

 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]

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]

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]

On the Flora of Antarctica

Musgo_Antartico.jpg

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 here. 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 )

Antarctic hair grass (Deschamsia antarctica)

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.

Antarctic_Pearlwort.jpg
 Antarctic pearlwort ( Colobanthus quitensis )

Antarctic pearlwort (Colobanthus quitensis)

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.

Moss_on_Aitcho_Island.jpg

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]

Meet the Crypts

26165576_2033477836679071_8698732942376159621_n.jpg

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

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

  Cryptocoryne cognata in situ .

Cryptocoryne cognata in situ.

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

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

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

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

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

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

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

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

  Cryptocoryne ligua

Cryptocoryne ligua

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

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

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

 The fruit of a  Cryptocoryne  is called a syncarp.

The fruit of a Cryptocoryne is called a syncarp.

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

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

  Cryptocoryne ciliata

Cryptocoryne ciliata

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

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

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

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

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

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

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

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

 

The Curious Case of the Yellowwood Tree

17975570426_efd4213146_o.jpg

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 is open for plenty of speculation, 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 do quite well 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 was 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.

17822773749_905eb83e49_o.jpg

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 site 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.

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. 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] [4]

Further Reading: [1] [2]

Saving One of North America's Rarest Shrubs

Arctostaphylos_franciscana_3.jpg

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.

Arctostaphylos_franciscana_-_Regional_Parks_Botanic_Garden,_Berkeley,_CA_-_DSC04529.jpg

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. 

PikiWiki_Israel_42124_Iris_Hermona.JPG

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

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

 A Eucerine bee visiting a nectar source. 

A Eucerine bee visiting a nectar source. 

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

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

PikiWiki_Israel_42126_Iris_Hermona.JPG

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

Borneo_rainforest.jpg

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 land.

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 it 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.

Logging_road_East_Kalimantan_2005.jpg
5551935164_127180a252_b.jpg

Scenarios like this play out all too often and sadly on a much larger scale than a backyard. Globally, forests have felt taken the brunt of human development. Though it is hard to get a sense of the scope of deforestation on a global scale, 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 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.

 Palm oil plantations where there once was rainforest. 

Palm oil plantations where there once was rainforest. 

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.

Rafflesia arnoldii in all of its glory.

Phalaenopsis_bellina_Orchi_01.jpg

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.

Paphiopedilum_philippinense_Orchi_021.jpg

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 one 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.

Peat_Forest_Swamp_(10712654875).jpg

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.

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 is a huge blow to global biodiversity.

Headhunter's_trail_Mulu_N._bicalcarata_3.jpg
  Nepenthes ampullaria  relies on decaying plant material within its pitcher for its nutrient needs.

Nepenthes ampullaria relies on decaying plant material within its pitcher for its nutrient needs.

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.

Pongo_tapanuliensis_female.jpg
 The flat-headed cat, an endemic of Borneo. 

The flat-headed cat, an endemic of Borneo. 

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] [12]

The Traveler's Palm

Penang_Malaysia_Ravenala-madagascariensis-01.jpg

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

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

Travellers-Palm-flower.jpg

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

tpalm.JPG

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.

Southern-ruffed-lemur-grooming.jpg

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

Ravenala_madagascariensis2.jpg

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

Southwestern Australia is home to one of the world's most unique floras. 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 unique 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 member of the 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 were overcome in some fascinating ways.

The way in which the grassplant manages this is quite 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.

Coupled with its underground roots, the grassplant is able to eek out a living. 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

Begoniaceae is a strange family. It consists of two genera - Begonia, which is comprised of 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.

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]

 

 

 

 

The Plant That Grows a Perch

For flowering plants, entering into an evolutionary relationship with birds as pollinators can be a costly endeavor. It can take a lot of energy to coax birds to their blossoms. On the whole, bird pollinated flowers are generally larger, sturdier, and produce more nectar. They tend to invest heavily in pigmentation. The plants themselves are often more robust as well. Unlike hummingbirds, which usually hover as they feed, other nectar-feeding birds require a perch. Often this is simply a stout branch or a stem, however, a plant endemic to South Africa takes bird perches to a whole new level - it grows one. 

Meet the rat's tail (Babiana ringens). Though not readily apparent, this bizarre looking plant is a member of the iris family. It is endemic to the Cape Province of South Africa where it can be found growing in sandy soils. It produces a fan of erect, grass-like leaves and, when conditions are right, a side branch full of red tubular flowers. This is when things get a bit strange. 

From that flowering stalk emerges a much longer stalk that is said to resemble the tail of a rat, earning this plant its common name. This stalk rises well above the rest of the flowers. If you look closely at the tip of this stalk you will quickly realize this is yet another flower stalk, though this one is sterile. Such a stalk may seem like a strange structure for this plant to produce until you consider its pollinators. 

The rat's tail has entered into an evolutionary relationship with a species of bird known as the malachite sunbird (Nectarina femosa). To access the nectar within, the malachite sunbird can't simply walk up to and shove its face down into the flowers. Instead, it must access them from above. To do so, it perches itself on the rigid sterile flower stalk. Once in position, the malachite sunbird can dip its long, down-curved beak directly into the flowers. This is exactly what the plant requires. In this perched position, pollen is brushed all over its chest. 

babssunny.jpg

Researchers wanted to know how obligate this relationship really was. By removing the perch on selected plants, they were able to demonstrate a reduction in pollination success . Specifically, male sunbirds were less likely to visit plants without the perch stalk. Although these plants are capable of self pollinating, like any sexually reproducing organism, outcrossing is the key to success. By offering the birds a sturdy perch allowing them exclusive access to their nectar, the plants guarantee sunbird fidelity.  

Photo Credits: [1] [2]

Further Reading: [1]

Pollination with a Twist

Ensuring that pollen from one flower makes it to another flower of that species is paramount to sexual reproduction in plants. It's one of the main drivers of the diversity in shapes, sizes, and colors we see in flowers across the globe. Sometimes the mechanism isn't so obvious. Take, for instance, the flowers of Impatiens frithii.

The flowers of this Cameroonian endemic have been a bit of a puzzle since its discovery. Like all Impatiens, they have a long nectar spur. However, the spur on I. frithii is uniquely curved. This puzzled botanists because most of the Impatiens in this region are pollinated by sunbirds. The curved spur would appear to make accessing the nectar within quite difficult for a bird. Still, just because we can't imagine it, doesn't mean that it's impossible. Something must pollinate this lovely little epiphyte in one way or another. This is where close observation comes in handy.

Thanks to remote cameras and lots of patience, botanists were able to record pollination events. They quickly realized that sunbirds are indeed the primary pollinator of this species. This was a bit of a surprise given the shape of the flower. However, the way in which the flowers deposit pollen on this birds is what is most remarkable. As it turns out, successful reproduction in I. frithii all comes down to that curved nectar spur. 

When a sunbird probes the flower for nectar, its beak follows the contour of the spur and this causes the entire flower to twist. As it twists, the anthers and stigma make contact with the chin of the bird. This is unlike other Impatiens which deposit the pollen on top of the heads of visiting birds.

Such an adaptation is quite remarkable in many ways. For one, it is elegantly simple. Such a small alteration of floral architecture is all that is required. Second, by placing pollen on the underside of the head, the plant guarantees that only pollen from its species will ever come into contact with the stigma. This is what we call reproductive isolation, which is an important driver in speciation.

Photo Credit: [1]

Further Reading: [1]

Important Lessons From Ascension Island

Located in the middle of the South Atlantic, Ascension Island is probably not on the top of anyone's travel list. This bleak volcanic island doesn't have much to offer the casual tourist but what it lacks in amenities it makes up for in a rich and bizarre history. Situated about 2,200 km east of Brazil and 3,200 km west of Angola, this remote island is home to one of the most remarkable ecological experiments that is rarely talked about. The roots of this experiment stem back to a peculiar time in history and the results have so much to teach the human species about botany, climate, extinction, speciation, and much more. What follows is not a complete story; far from it actually. However, my hope is that you can take away some lessons from this and, at the very least, use it as a jumping off point for future discussions. 

Ascension Island is, as land masses go, quite young. It arose from the ocean floor a mere 1 million years ago and is the result of intense volcanic activity. Estimates suggest that volcanism was still shaping this island as little as 1000 years ago. Its volcanic birth, young age, isolated conditions, and nearly non-existent soils meant that for most of its existence, Ascension Island was a depauperate place. It was essentially a desert island. Early sailors saw it as little more than a stopover point to gather turtles and birds to eat as they sailed on to other regions. It wasn't until 1815 that any permanent settlements were erected on Ascension. 

In looking for an inescapable place to imprison Napoleon Bonaparte, the Royal Navy claimed Ascension in the name of King George III. Because Napoleon had a penchant for being an escape artist, the British decided to build a garrison on the island in order to make sure Napoleon would not be rescued. In doing so, the limitations of the island quickly became apparent. There were scant soils in which to grow vegetables and fresh water was nearly nonexistent. 

The native flora of Ascension was minimal. It is estimated that, until the island was settled, only about 25 to 30 plant species grew on the island. Of those 10 (2 grasses, 2 shrubs, and 6 ferns) were considered endemic. If the garrison was to persist, something had to be done. Thus, the Green Mountain garden was established. British marines planted this garden at an elevation of roughly 2000 feet. Here the thin soils supported a handful of different fruits and vegetables. In 1836, Ascension was visited by a man named Charles Darwin. Darwin took note of the farm that had developed and, although he admired the work that was done in making Ascension "livable" he also noted that the island was "destitute of trees."

 One of Ascension Island's endemic ferns -  Pteris adscensionis

One of Ascension Island's endemic ferns - Pteris adscensionis

Others shared Darwin's sentiment. The prevailing view of this time period was that any land owned by the British empire must be transformed to support people. Thus, the wheels of 'progress' turned ever forward. Not long after Darwin's visit, a botanist by the name of Joseph Hooker paid a visit to Ascension. Hooker, who was a fan of Darwin's work, shared his sentiments on the paucity of vegetation on the island. Hooker was able to convince the British navy that vegetating the island would capture rain and improve the soil. With the support of Kew Gardens, this is exactly what happened. Thus began the terraforming of Green Mountain.

For about a decade, Kew shipped something to the tune of 330 different species of plants to be planted on Ascension Island. The plants were specifically chosen to withstand the harsh conditions of life on this volcanic desert in the middle of the South Atlantic. It is estimated that 5,000 trees were planted on the island between 1860 and 1870. Most of these species came from places like Argentina and South Africa. Soon, more plants and seeds from botanical gardens in London and Cape Town were added to the mix. The most incredible terraforming experiment in the world was underway on this tiny volcanic rock. 

By the late 1870's it was clear the the experiment was working. Trees like Norfolk pines (Araucaria heterophylla), Eucalyptus spp. and figs (Ficus spp.), as well as different species of banana and bamboo had established themselves along the slopes of Green Mountain. Where there was once little more than a few species of grass, there was now the start of a lush cloud forest. The vegetation community wasn't the only thing that started to change on Ascension. Along with it changed the climate. 

Estimates of rainfall prior to these terraforming efforts are sparse at best. What we have to go on are anecdotes and notes written down by early sailors and visitors. These reports, however, paint a picture of astounding change. Before terraforming began, it was said that few if any clouds ever passed overhead and rain rarely fell. Those living on the island during the decade or so of planting attested to the fact that as vegetation began to establish, the climate of the island began to change. One of the greatest changes was the rain. Settlers on the island noticed that rain storms were becoming more frequent. Also, as one captain noted "seldom more than a day passes over now without a shower or mist on the mountain." The development of forests on Ascension were causing a shift in the island's water cycle. 

Plants are essentially living straws. Water taken up by the roots travels through their tissues eventually evaporating from their leaves. The increase in plant life on the island was putting more moisture into the air. The humid microclimate of the forest understory cooled the surrounding landscape. Water that would once have evaporated was now lingering. Pools were beginning to form as developed soils retained additional moisture.

Now, if you are anything like me, at this point you must be thinking to yourself "but what about the native flora?!" You have every right to be concerned. I don't want to paint the picture that everything was fine and dandy on Ascension Island. It wasn't. Even before the terraforming experiment began, humans and other trespassers left their mark on the local biota. With humans inevitably comes animals like goats, donkeys, pigs, and rats. These voracious mammals went to work on the local vegetation. The early ecology that was starting to develop on Ascension was rocked by these animals. Things were only made worse when the planting began.

Of the 10 endemic plants native to Ascension Island, 3 went extinct, having been pushed out by all of the now invasive plant species brought to the island. Another endemic, the Ascension Island parsley fern (Anogramma ascensionis) was thought to be extinct until four plants were discovered in 2010. The native flora of Ascension island was, for the most part, marginalized by the introduction of so many invasive species. This fact was not lost of Joseph Hooker. He eventually came to regret his ignorance to the impacts terraforming would have on the native vegetation stating “The consequences to the native vegetation of the peak will, I fear, be fatal, and especially to the rich carpet of ferns that clothed the top of the mountain when I visited it." Still, some plants have adapted to life among their new neighbors. Many of the ferns that once grew terrestrially, can now be found growing epiphytically among the introduced trees on Green Mountain. 

 The Ascension Island parsley fern ( Anogramma ascensionis )

The Ascension Island parsley fern (Anogramma ascensionis)

Today Ascension Island exists as a quandary for conservation ecologists. On the one hand the effort to protect and conserve the native flora and fauna of the island is of top priority. On the other hand, the existence of possibly the greatest terraforming effort in the world begs for ecological research and understanding. A balance must be sought if both goals are to be met. Much effort is being put forth to control invasive vegetation that is getting out of hand. For instance, the relatively recent introduction of a type of mesquite called the Mexican thorn (Prosopis juliflora) threatens the breeding habitat of the green sea turtle. Efforts to remove this aggressive species are now underway. Although it is far too late to reverse what has been done to Ascension Island, it nonetheless offers us something else that may be more important in the long run: perspective.

If anything, Ascension Island stands as a perfect example of the role plants play in regulating climate. The introduction of these 330+ plant species to Ascension Island and the subsequent development of a forest was enough to completely change the weather of that region. Where there was once a volcanic desert there is a now a cloud forest. With that forest came clouds and rain. If adding plants to an island can change the climate this much, imagine what the loss of plants from habitats around the world is doing. 

Each year an estimated 18 million acres of forest are lost from this planet. As human populations continue to rise, that number is only going to get bigger. It is woefully ignorant to assume that habitat destruction isn't having an influence on global climate. It is. Plants are habitat and when they go, so does pretty much everything else we hold near and dear (not to mention require for survival). If the story of Ascension does anything, I hope it serves as a reminder of the important role plants play in the function of the ecosystems of our planet. 

 The endemic Ascension spurge ( Euphorbia origanoides )

The endemic Ascension spurge (Euphorbia origanoides)

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

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

 

A Green Daffodil From Spain

22597693024_9a683923cc_b.jpg

There are some plants that are so ubiquitous in horticulture that I almost forget that they have wild constituents. Every plant in our gardens can trace its lineage back to the wild. As is often the case, I find the wild congeners of our most beloved horticultural curiosities to be far more fascinating. Take, for instance, the genus Narcissus. Who doesn't recognize a daffodil? The same cannot be said for their wild cousins. In fact, there exists some pretty fantastic species within this genus including a small handful of species that flower in autumn. 

One of the most unique among the fall flowering daffodils is a species known scientifically as Narcissus viridiflorus. This lovely little plant is quite restricted in its range. You will only find it growing naturally in a small region around Gibraltar where it is restricted to rich, clay and/or rocky soils. During years when it is not in flower, N. viridiflorus produces spindly, rush-like leaves. As such, it can be hard to find. 

 

Narcissus_viridiflorus_2.jpg

When Narcissus viridiflorus does decide to flower, it forgoes leaf production. From the bulb arises a single green scape. From that scape emerges the flower. The flowers of this bizarre daffodil are decidedly not very daffodil-like. They are rather reduced in form, with long, slender green petals and a nearly nonexistent daffodil cone. Also, they are green. Though I have not seen this investigated directly, it has been suggested that the green scape and flowers contain enough chlorophyll that they plant can recoup at least some of the energy involved in producing flowers and eventually seed. 

The flowers themselves open at night and are said to be very fragrant. Again, no data exists on who exactly pollinates this species but the timing, color, and smell all suggest nocturnal insects like moths. Like the other daffodils of this region, Narcissus viridiflorus is poorly understood. Taken in combination with its limited distribution one can easily see how such a species may be quite vulnerable to human disturbance. As it stands now, this species and many of its cousins are no more than horticultural curiosities for more niche bulb societies. In other words, Narcissus viridiflorus is in need of some real attention. 

Photo Credit: [1] [2]

Further Reading: [1]

On the Wood Rose and its Bats

New Zealand has some weird nature. It is amazing to see what an island free of any major terrestrial predators can produce. Unfortunately, ever since humans found their way to this unique island, the ecology has suffered. One of the most unique plant and animal interactions in the world can be found on this archipelago but for how much longer is the question.

The story starts with a species of bat. In fact, this bat is New Zealand's only native terrestrial mammal. That's right, I said terrestrial. The New Zealand lesser short-tailed bat spends roughly 40% of its time foraging for insects on the ground. It has lots of specialized adaptations that I won't go into here but the cool part is they forage in packs, stirring up insects from the leaf litter until they reach a level of feeding frenzy that I thought was only reserved for sharks or piranhas. Along with using echo location, they also have a highly developed sense of smell. This is important for our second player in this forest floor drama.

Enter Dactylanthus taylorii, the wood rose. This plant is not a rose at all but rather a member of the tropical family Balanophoraceae. More importantly, it is parasitic. It produces no chlorophyll and lives most of its life wrapped around the roots of its host tree underground. Every once in a while a small patch of flowers break through the dirt and just barely peak above the leaf litter. This give this species it's Māori name of "pua o te reinga" or "pua reinga", which translates to "flower of the underworld." The flowers emit a musky, sweet smell that attracts these ground foraging bats. The bats are one of the only pollinators left on the island. They sniff out the flowers and dine on the nectar, all the while being dusted with pollen. Recently, it has been found that New Zealand's giant ground parrot, the kakapo, is also believed to have been a pollinator of this plant. Sadly, today the kakapo exists solely on one small island of the New Zealand archipelago.

Both the wood rose and the New Zealand lesser short-tailed bat are considered at risk for extinction. When modern man came to these islands they brought with them the general suite of mammalian invasives like rats, mongoose, cats, and pigs, which are exacting a major toll on the local ecology. The plants and animals native to New Zealand have not shared an evolutionary history with such aggressive mammalian invaders and thus have no adaptations for coping with their sudden presence. The future of the wood rose, the New Zealand lesser short-tailed bat, and the kakapo, along with many other uniquely New Zealand species are for now uncertain.

Photo Credits: Joseph Dalton Hooker (1859) and Nga Manu Nature Reserve (http://www.ngamanu.co.nz/)

Further Reading:

http://bit.ly/2bBw8FT

http://bit.ly/2bKRY90

http://bit.ly/2bKpxfE

The Amazing Radiation of Hawaii's Lobeliads

Hawai'i is home to so many interesting species of plants, many of which are found nowhere else in the world. One group, however, stands out among the rest in that it represents the largest plant radiation not just in Hawai'i but on any island archipelago in the world!

I am of course talking about the Hawaiian lobelioids. We are familiar with species found on North America, which include the lovely cardinal flower (Lobelia cardinalis) and the great blue lobelia (Lobelia siphilitica), but the 6 genera that comprise the Hawaiian radiation are something quite different altogether.

Numbering roughly 125 species in total (and many extinct species as well), it was long thought that they were the result of at least 3 separate invasions. Thanks to recent DNA analysis, it is now believed that all 6 genera are the result of one single invasion by a lobelia-like ancestor. This may seem ridiculous but, when you consider the fact that this invasion happened back when Gardner Pinnacles and French Frigate Shoals were actual islands and none of the extant islands were even in existence, then you can kind of grasp the time scales involved that produced such a drastic and varied radiation.

Sadly, like countless Hawaiian endemics, the invasion of the human species has spelled disaster. Hawaiian endemics are declining at an alarming rate. Introduced pigs and rats eat seeds, devour seedlings, and even go as far as to chew right through the stems of adult plants. To make matters worse, many species evolved to a specific suite of pollinators. Take the genus Clermontia for example. The flowers of these species are evolved for pollination by the island's endemic honey creepers. Due to avian malaria and other human impacts, many honey creepers are endangered and some have already gone extinct. Without their pollinators, many of these lobelioids are doomed to slow extinction if they haven't disappeared already. For some, what few populations remain are now fenced off and have to be hand pollinated. As I have said all too often, the future of this great radiation of plants is uncertain.

Photo Credits: Oakapples (http://bit.ly/OjOqhU), Forest and Kim Starr (http://bit.ly/1miCAA5), Dave Janas

Further Reading:

http://bit.ly/2aIviF5

http://bit.ly/2bh9Dpv

http://bit.ly/2b4i5dV

Meeting Amborella trichopoda

When I found out I would be seeing a living Amborella, a lump formed in my throat. There I was standing in one of the tropical houses at the Atlanta Botanical Garden trying to keep my cool. No amount of patience was ample enough to quell my excitement. How was I going to react? How big were these plants? Would I see flowers? Could I touch them? What were they growing in? My curiosity was through the roof.

Naturally this sort of excitement is reserved for those of us familiar with Amborella trichopoda. This strange shrub is not something that would readily stand out against a backdrop of tropical flora. However, if life history and ecology were to be translated into outward appearances, Amborella would likely be one of the most gaudy plants on this planet. What I was about the lay eyes on is the only member of the sole genus belonging to the family Amborellaceae, which is the sole member of the order Amborellales.

Even more exciting is its position on the angiosperm family tree. As flowering plants go, Amborella is thought to be the oldest alive today. Okay, so maybe this shrub isn't the oldest flowering plant in the world. It is likely that at one time, many millions of years ago, there were more representatives of Amborellaceae growing on this planet. Until we turn up more fossil evidence it is nearly impossible to say. Still, Amborella's place in the story of flowering plant evolution is consistently located at the base.

That is not to say that this shrub is by any means primitive. I think the first thing that shocked me about these plants is just how "normal" they appear. Sans flowers, I didn't see much out of the ordinary about them. They certainly look like they belong on our timeline. Without proper training in plant anatomy and physiology, there is little one could deduce about their evolutionary position. Regardless of my ignorance on plant morphology, there is plenty to look at on Amborella.

For starters, Amborella has tracheids but no vessel elements, making its vascular system more like that of a gymnosperm than an angiosperm. Its small flowers are borne in the axils of the evergreen leaves. It has no petals, only bracts arranged into a spiral of tepals. The female flowers consist of 4 to 8 free carpels and do not produce a style. Male flowers look like nothing more than a spiral cluster of stamens borne on short filaments.

If plant anatomy isn't enough to convince you, then the genetic analyses tell a much more compelling story. DNA sequencing consistently places Amborella at the base of the flowering plant family tree. Again, this is not to say that this shrub is by any means "primitive" but rather its lineage diverged long before what we would readily recognize as a flowering plant evolved. As such, Amborella offers us a window into the early days of flowering plants. By comparing traits present in more derived angiosperms to those of Amborella, researchers are able to better understand how the most dominant group of plants found their place in this world.

Another interesting thing happened when researchers looked at the DNA of Amborella. What they found was more than just Amborella genes. Inside the mitochondrial DNA are an unprecedented amount of foreign DNA from algae, lichens and mosses. In fact, an entire chunk of DNA corresponded to an entire mitochondrial genome of a moss! Researchers now believe that this is a case of extreme horizontal gene transfer between Amborella and its neighbors both growing on and around it. Both in the wild and in cultivation, Amborella is covered in a sort of "biofilm." Whether or not such gene transfer has assisted in the conservatism of this lineage over time remains to be seen.

At this point you may be asking how this lineage has persisted for over 130 million years. For the most part, it is probably due to chance. However, there is one aspect of its ecology that really stands out in this debate and that is its geographic distribution. Amborella is endemic to Grande Terre, the main island of New Caledonia. This is a very special place for biodiversity.

New Caledonia is a small fragment of the once great super-continent Gondwana. New Caledonia, which was part of Australia at that time, broke away from Gondwana when the super-continent began to break up some 200-180 million years ago. New Caledonia then broke away from Australia some 66 million years ago and has not been connected to another land mass since. A warm, stable climate has allowed some of the most unique flora and fauna to persist for all that time. Amborella is but one of the myriad endemic plants that call New Caledonia home. For instance, 43 species of tropical conifers that grow on these small islands are found nowhere else in the world. The whole region is a refugia of a long lost world.

Being a biodiversity hot spot has not spared New Caledonia from the threats of modern man. Mining, agriculture, urbanization, and climate change are all threatening to undo much of what makes this place so unique. The loss of a species like Amborella would be a serious blow to biodiversity, conservation, and the world as whole. We cannot allow this species to exist only in cultivation. New Caledonia is one place we must desperately try to conserve. Meeting this species has left a mark on me. Being able to observe living Amborella up close and personal is something I will never forget as my chances of seeing this species in the wild are quite slim. I am so happy to know that places like the Atlanta Botanical Garden are committed to understanding and conserving this species both in the wild and in cultivation. For now Amborella is here to stay. Long may it be that way.

 

Further Reading:

http://bit.ly/29MuMuw

http://bit.ly/29MuML0

http://bit.ly/29ZKNJS

 

Lovely Lomatium

I officially learned how to botanize in the American west. Before then my skills were limited to "hey, look at the pretty flower" and then Googling my way to an answer. As such, I have a real soft spot for western botany. Despite the fact that I have not had the chance to exercise those muscles in some time, I nonetheless revisit the few groups that I do remember via the massive photo collection I built up during my tenure in Wyoming. One group I am particularly fond of are members of the genus Lomatium.

I had never really paid attention to members of the carrot family. I always associated that group with the Queen Anne's lace (Daucus carota) I encountered growing in ditches. In other words, I found them boring. All of that changed when I moved to Wyoming. Spring was slow to start that year. I mean really slow. I thought I had it bad in western New York where spring snow storms and freezing temperatures often delayed plant growth well into May. That year in Wyoming, the last snow storm hit on June 29th. Because of this, most of the plants we were trying to locate were biding their time underground waiting for favorable weather to kick off the growing season.

By mid June I was starving for plant life. I needed to see some greenery. That is when I first laid eyes on a Lomatium. They began appearing as tight clusters of highly dissected, rubbery leaves. Once I knew what to look for, I began finding them throughout the foothill regions where we were working. Since I was just getting familiar with the local flora, I was hard pressed to key anything out. Instead I just waited for flowers. I didn't have to wait very long. 

Soon entire hillsides were covered in little yellow umbels. They were squat plants, never growing too high. The constant winds that whipped across the terrain made sure of that. It soon became apparent that Lomatiums don't waste any time. Water is limited in these habitats and they have to make quick work of it while it is available. Another interesting thing to note is the sex of the flowers. Generally when I see a dense umbel like that, I just assumed they were hermaphroditic. In at least some Lomatium, this is actually not the case. The sex of the flowers is determined by age. 

Smaller plants tend to produce male flowers, whereas larger plants will produce hermaphrodites. This makes a lot of sense as producing only pollen requires much fewer resources than producing ovaries and eventually seeds. Needless to say, larger plants also produce the most seed and are often the driving force in population persistence and growth. The seeds themselves are quite interesting. They are winged and often quite fleshy until they dry. Wind is the predominant seed dispersal mechanism and there is no shortage of wind in sagebrush country. 

The phylogeny of this genus is quite confusing. I certainly haven't gotten my head wrapped around it. Individuals are notoriously hard to identify both physically and genetically. There is a large degree of genetic variation between plants and "new species" are still being discovered. At the same time, there is also a lot of endemism and some species like Lomatium cookii and Lomatium dissectum are of conservation concern. Aside from habitat destruction, over-grazing, and limited ranges, over-collection for herbal uses poses considerable threat to many species. 

Further Reading:

http://bit.ly/1VWvMfV

http://bit.ly/1VE24MF

http://bit.ly/1WUzohQ

http://bit.ly/1qXSVS8

http://bit.ly/245NDpH

A New Species of Parasite Discovered in Japan

A new species of parasitic plant has been discovered on the Japanese island of Yakushima. A small population was found by Suetsugu Kenji during a survey of the lowland laurel forests that cover much of the island. Despite being an authority on parasitic plants of this region, Professor Suetsugu did not recognize these plants. As such, a specimen was collected for a closer look.

An in depth examination revealed that this was indeed a new species. It has been named Sciaphila yakushimensi in honor of the island on which it was discovered. It belongs to a family of plants called Triuridaceae. They are closely related to the family Alismataceae and many members of this family have foregone photosynthesis for a parasitic lifestyle.

S. yakushimensi is what we call a mycoheterotroph. It parasitizes mycorrhizal fungi, taking the nutrients it needs and giving nothing in return. The fungi themselves are getting their nutrient needs from the trees that grow in the forest. As such, S. yakushimensi could not exist without an intact forest to support its fungal host.

This is the troubling part. Only two populations of S. yakushimensi have been discovered. Its parasitic lifestyle makes it difficult to get an accurate estimation of its numbers. These plants live most of their lives underground, only appearing when it is time to flower. Because of this, researchers are already suggesting that this species be considered endangered.

Sadly, its native forest is under constant threat of logging. Much of this region remains unprotected. Since mycoheterotrophs like S. yakushimensi rely on an intact forest capable of supporting its host fungi, any disturbance that threatens the forest can spell disaster for these parasites. Far from being a detriment to the forests in which they live, parasitic plants like S. yakushimensi can serve as a very important reminder of how crucial it is to preserve entire ecosystems rather than single species.

Photo Credit: Yamashita Hiroaki

Further Reading:

https://www.tsumura.co.jp/english/kampo/plant/090/090_01.html

The World's Largest Flower

Have you ever wondered which plants produce the largest single flower in the world?

Meet Rafflesia. Well, I should say Rafflesia arnoldii, which produces flowers that are over 3 feet (1 meter) in diameter and can weigh as much as 24 lbs. (11 kg)! Rafflesia is a genus that contains roughly 28 species that hail from the jungles of southeastern Asia. What is crazy about this genus is not just the fact that it produces the largest flower in the world, but also that they are all holoparasites. They do not produce stems, leaves, or true roots. They live out their entire lives inside of a group of vines related to North America's grapes. Except for flowering, Rafflesia exists entirely as a network of mycelium-like cells inside their vine hosts.

For a long time, the taxonomic status of this plant was highly debated but recent DNA evidence puts it in the order Malpighiales. From there, things get a little funny. One recent analysis suggested that Rafflesia belonged in the family Euphorbiaceae, however, it most likely warrants its own family - Rafflesiaceae.

 A view from the inside of another species of Rafflesia - Rafflesia tuan-mudae. The strangely spiked "disk" in the center is the column, which houses the reproductive organs.  Photo by Ch'ien C. Lee

A view from the inside of another species of Rafflesia - Rafflesia tuan-mudae. The strangely spiked "disk" in the center is the column, which houses the reproductive organs.

Photo by Ch'ien C. Lee

So, why produce such large flowers? Well, existing solely within a vine makes it hard to establish a large population in any given area, a difficult situation for any plants that rely on pollinators for reproduction. By growing very large and thus being able to produce a lot of "stink" (this plant is also referred to as the corpse plant), Rafflesia make sure that pollinators will come from far and wide to investigate, thus increasing their chances of cross pollinating. How this plant goes about spreading its seeds is still a mystery.

Most interesting of all, it has been discovered that there is some amount of horizontal gene transfer going on between Rafflesia and its host. Basically, Rafflesia obtains strands of DNA from the vine it lives in and uses them in its own genetic code. It is believed this incurs some fitness benefit to Rafflesia but it is yet not fully understood.

Sadly, many species within this family may be lost before we ever get a chance to get to know them better. Forests in this region are disappearing rapidly to make room for expanding populations and agriculture. What makes matters worse for the genus is that their lifestyle makes them very hard to study. It is especially difficult to obtain accurate population estimates. As more and more forest is cleared, we could be losing countless populations of these wonderful and intriguing plants. As with large mammals, it would seem that the world's largest flower is falling victim to the unending tide of human development.

Photo Credit: Tamara van Molken

and

Ch'ien C. Lee www.wildborneo.com.my/photo.phpf=cld05120647.jpg

Further Reading:

http://journals.plos.org/plosgenetics/article?id=10.1371%2Fjournal.pgen.1003265

http://www.sciencedirect.com/science/article/pii/S0960982208013432

http://legacy.earlham.edu/~givenbe/Rafflesia/rafflesia/biodiv2.htm