Buckthorns Gone Wild

Colletia paradoxa photo by James Gaither licensed by CC BY-NC-ND 2.0

Colletia paradoxa photo by James Gaither licensed by CC BY-NC-ND 2.0

When I think of the buckthorn family (Rhamnaceae), my mind conjures up images of battling with Rhamnus invasions around the Great Lakes or the amazing diversity of Ceanothus in western North America. Never have my thoughts drifted to the bizarre and wonderful genus Colletia. Native to temperate regions of South America, this strange group of spiny shrubs is certainly worth a closer look.

Though new to me, the genus Colletia has been known to science and horticulture since at least the late 1700’s. Hailing from temperate climates, at least two of the five known species of Colletia have found there way into temperate gardens elsewhere. Who could blame gardeners for their fascination with these shrubs. Close inspection of Colletia reveals surprisingly complex morphological features.

Colletia paradoxa

Colletia paradoxa

For starters, those large, thick, leaf-like thorns are not leaves at all. They are flattened extensions of the stem called cladodes. Instead of relying on leaves for most of their photosynthetic needs, the various Colletia instead produce chlorophyll in their stems. The cladodes function in much the same way as leaves in that their increased surface area maximizes photosynthetic potential. It is likely that cladodes are a means of conserving valuable resources for the plant.

Instead of producing vulnerable leaves that are subject to plenty of damage, these shrubs simply utilize stem tissues. Stems don’t need to be regrown year after year and by adorning the tips of the cladodes with spines, the plant is better able to protect its photosynthetic tissues. That is not to say that Colletia produce no leaves at all. Colletia will produce leaves near the base of each cladode, especially on younger tissues. Leaves, however, are deciduous and don’t stick around long enough to do much photosynthesizing.

Colletia ulicina with its red, tubular flowers. Photo by FarOutFlora licensed by CC BY-NC-ND 2.0

Colletia ulicina with its red, tubular flowers. Photo by FarOutFlora licensed by CC BY-NC-ND 2.0

The flowers of Colletia ulicina are pollinated by hummingbirds. photo by James Gaither licensed by CC BY-NC-ND 2.0

The flowers of Colletia ulicina are pollinated by hummingbirds. photo by James Gaither licensed by CC BY-NC-ND 2.0

Colletia are made all the more noticeable when they come into flower. For most species, clusters of lightly-scented, white flowers are produced at the base of the cladodes. For these species, insects are thought to be the predominant pollinators. Such is not the case for Colletia ulicina. This species produces sprays of bright red, tubular flowers along its stems. In the wild, these are pollinated by the green-backed firecrown hummingbird (Sephanoides sephaniodes).

Another interesting aspect of Colletia ecology is that they are all nitrogen fixers. To be fair, the plants themselves don’t do any of the fixing. Instead, they produce tiny structures on their roots called “nodules,” and those nodules house specialized bacteria collectively referred to as actinomycetes. In exchange for carbohydrates produced via photosynthesis, these bacteria fix nitrogen from the air. This extra boost of nitrogen allows Colletia to survive and excel in the nutrient-poor soils they call home.

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

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

The Nitrogen-Fixing Abilities of Cycads

Photo by Daderot Public Domain

Photo by Daderot Public Domain

Long before the first legumes came onto the scene, the early ancestors of Cycads were hard at work fixing atmospheric nitrogen. However, they don't do this on their own. Despite being plentiful in Earth's atmosphere, gaseous nitrogen is not readily available to most forms of life. Only a special subset of organisms are capable of turning gaseous nitrogen into forms usable for life. Some of the first organisms to do this were the cyanobacteria, which has led them down the path towards symbioses with various plants on many occasions. 

Cycads are but one branch of the gymnosperm tree. Their lineage arose at some point between the Carboniferous and Permian eras. Throughout their history it would seem that Cycads have done quite well in poor soils. They owe this success to a partnership they struck up with cyanobacteria. Although it is impossible to say when exactly this happened, all extant cycads we know of today maintain this symbiotic relationship with these tiny prokaryotic organisms. 

Cross section of a coralloid cycad root showing the green cyanobacteria inside. Photo by George Shepherd licensed under CC BY-NC-SA 2.0

Cross section of a coralloid cycad root showing the green cyanobacteria inside. Photo by George Shepherd licensed under CC BY-NC-SA 2.0

The relationship takes place in Cycad roots. Cycads don't germinate with cyanobacteria in tow. They must acquire them from their immediate environment. To do so, they begin forming specialized structures called precoralloid roots. Unlike other roots that generally grow downwards, these roots grow upwards. They must situate themselves in the upper layer of soil where enough light penetrates for cyanobacteria to photosynthesize.

The cyanobacteria enter into the precoralloid roots through tiny cracks and take up residence. This causes a change in root development. The Cycad then initiates their development into true coralloid roots, which will house the cyanobacteria from that point on. Cycads appear to be in full control of the relationship, dolling out carbohydrates in return for nitrogen depending on the demands of their environment. Coralloid roots can shed and reform throughout the lifetime of the plant. It is quite remarkable to think about how nitrogen-fixing symbiotic relationships between plants and microbes have evolved independently throughout the history of life on this planet.

Photo Credits: [1] [2]

Further Reading: [1] [2]

 

Meet the Sweetfern

Photo by Sten Porse licensed under CC BY-SA 3.0

Photo by Sten Porse licensed under CC BY-SA 3.0

I remember the first time I laid my eyes on Comptonia peregrina. I was new to botany at that point in my life so I didn't have a well developed search image for these sorts of things. I was scrambling down a dry ridge with a scattered overstory of gnarly looking chestnut oaks when I saw a streak of green just below me on a sandy outcropping. They were odd looking plants, the likes of which I had never seen before.

I took out my binoculars to get a better look. What were these strange organisms? Were they ferns? No, they seemed to have woody stems. Were they gymnosperms? No, I could make out what appeared to be male catkins. Luckily I never leave home without a field guide or two. Using what little terminology I knew, I was able to narrow my focus to a plant commonly called a "sweetfern."

Photo by Megan Hansen licensed under CC BY-SA 2.0

Photo by Megan Hansen licensed under CC BY-SA 2.0

This was one of the first instances in which I grasped just how troublesome common names can be. C. peregrina is mostly definitely not a fern. It is actually an angiosperm that hails from the bay family (Myricaceae). Comptonia is a monotypic genus, with C. peregrina being the only species. It is a denizen of dry, nutrient poor habitats. As such, it has some wonderful adaptations to deal with these conditions.

To start with, its a nitrogen fixer. Similar to legumes, it forms nodules on its roots that house specialized nitrogen-fixing bacteria called rhizobia. This partnership takes care of its nitrogen needs, but what about others? One study found that not only do the roots form nodules, they also form dense cluster roots. Oddly, closer observation found that these clusters were not associated with mycorrhizal fungi. What's more, they also found that these structures were most prevalent in highly disturbed soils. It is thought that this is one way that the plant can maximize its uptake of phosphorus under the harshest growing conditions. 

Photo by Jomegat licensed under CC BY-SA 3.0

Flowering in this species is not a showy event. C. peregrina can be monoecious or dioecious, producing male and female catkins towards the ends of its shoots. After fertilization, seeds develop inside bristly fruits. Seed banking appears to be an important reproductive strategy for this species. One study found that germinated seeds had lain dormant in the soil for over 70 years until disturbance opened up the canopy above. It is expected that seeds of this species could exhibit dormancy periods of a century or more. 

In total, this is one spectacular species. Not only does it have a unique appearance, it is also extremely hardy and an excellent species to plant in drought-prone soils wherever it is native. I do see it in landscaping from time to time. If you encounter this species in the wild, take the time to observe it in detail. You will be happy you did!

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

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

Of Gunnera and Cyanobacteria

Photo by UnconventionalEmma licensed under CC BY-NC 2.0

Photo by UnconventionalEmma licensed under CC BY-NC 2.0

Nitrogen is a limiting resource for plants. It is essential for life functions and yet they do not produce it on their own. Instead, plants need to get it from their environment. They cannot uptake gaseous nitrogen, which is a shame because it makes up 78.09% of our atmosphere. As such, some plants have developed very interesting ways of obtaining nitrogen from their environment. Some, like the legumes, produce special nodules on their roots, which house bacteria that fix atmospheric nitrogen. Other plants utilize certain species of mycorrhizal fungi. One family of plants, however, has evolved a symbiotic relationship that is unlike any other in the angiosperm world.

A Gunnera inflorescence.  Photo by Lotus Johnson licensed under CC BY-NC 2.0

A Gunnera inflorescence. Photo by Lotus Johnson licensed under CC BY-NC 2.0

Meet the Gunneras. This genus has a family all to itself - Gunneraceae. They can be found in many tropical regions from South America to Africa and New Zealand. Some species of Gunnera are small while others, like Gunnera manicata, have leaves that can be upwards of 6 feet in diameter. Their leaves are well armed with spikes and spines. All in all they are rather prehistoric looking. The real interesting thing about the Gunneras though, is in the symbiotic relationship they have formed with cyanobacteria in the genus Nostoc.

Traverse section of a Gunnera stem showing cyanobacteria colonies (C) and the cup-like structures (S) where they enter the stem. [SOURCE]

Traverse section of a Gunnera stem showing cyanobacteria colonies (C) and the cup-like structures (S) where they enter the stem. [SOURCE]

Gunnera produce cuo-like glands that house these cyanobacteria. The glands are filled with a special mucilage that not only attracts the cyanobacteria, but also stimulates it to grow. Once inside the glands, the cyanobacteria begins to grow into the plant, eventually fusing with the Gunnera cells. From there the cyanobacteria earn their keep by producing copious amounts of usable nitrogen and in return, the Gunnera supplies carbohydrates. This relationship is amazing and quite complex. It also offers researchers an insight into how such symbiotic relationships evolve.

Photo Credit: [1] [2] [3]

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