Cedar Confusion

This is a guest post by Jeremiah Sandler. Words by Jeremiah. Photos by Daniel Murphy (except where noted).

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What makes a cedar a cedar?

I recently asked this question to a professor of mine because I kept hearing individuals in the field refer to many different species as “cedars”. It was puzzling to me because, being the taxonomy-nerd that I am, most of these plants are in entirely different plant families but still called the same thing. Yes, sometimes common names overlap with one another regionally; avoiding that mix up is the purpose of binomial nomenclature in the first place! So, what gives?! Why are 50+ different species all called cedars?

This professor is a forester, not a botanist. He told me the word “cedar” describes the wood. Turns out, after some research and conversation, that’s all there was to it. As defined by Google, a cedar is:

Any of a number of conifers that typically yield fragrant, durable timber, in particular.

Cedar wood is a natural repellent of moths, is resistant to termites, and is rot resistant. A good choice of outdoor lumber.

I was hoping to find either a phylogenetic or taxonomic answer to what makes a cedar a cedar. I didn’t. Taxonomic relationships between organisms are one of the most exciting parts of biology. Thankfully, some solace was found in the research:

There are true cedars and false cedars.

True cedars are in the family Pinaceae and in the genus Cedrus. Their leaves are short, evergreen needles in clusters. The female cones are upright and fat, between 3 – 4 inches long. Their wood possesses cedar quality, and they are native to the Mediterranean region and the Himalayas.

False cedars are in the family Cupressaceae, mostly in the following genera: Calocedrus, Chamaecyparis, Juniperus, and Thuja. Their leaves are scale-y, fan-like sprays. Female cones are very small, about half an inch long, and remain on the tree long after seed dispersal. The bark is often both reddish and stringy or peely. Their wood possesses cedar quality. It is easy to separate them from true cedars, but less obvious to tell them from one another. These false cedars are native to East Asia and northern North America.

I couldn’t do away with the umbrella term “cedar.” Every naturalist can agree that one of the most pleasurable things while outdoors looking at plants is identifying them. I have set a new objective to correctly identify and differentiate between all of the cedars and false cedars, rather than simply calling them cedars. I guess I’m just fussy like that.

What Do Desert Tortoises Eat?

Desert conditions are not intuitively conducive to life. In many regards they are extreme. Blistering, bleak, dry, and barren. The desert is a place unsuited for the faint of heart and the ill-equipped. Broadly speaking, life in the desert is reliant on one of two things: technology or evolutionary adaptation. Like many species native to desert environments, the desert tortoise employs the latter. It is at home in the desert because it evolved there. That is not to say that life is always easy for the desert tortoise and species like it, but it is possible, thanks to hundreds of thousands of years of making it work. As John Alcock puts it in, Sonoran Desert Spring, “the tortoise will deal with its environment through evolved design rather than seek to deny the desert its due.”

Perhaps it is because the desert is such a harsh environment, requiring finely tuned adaptations for survival, that sweeping changes can put resident species in peril – threatening their long-term existence. The desert tortoise is an example of this. Since 1990, Gopherus agassizii has found itself listed as threatened under the U.S. Endangered Species Act [it is categorized as vulnerable by the IUCN] due to significant population declines and loss of habitat. Getting there did not happen overnight, and it is impossible to pinpoint a sole cause of the tortoise’s decline. Instead, a suite of things have conspired against it, making it difficult to decide on the best route towards conservation.

In an October 2012 issue of BioScience, Averill-Murray, et al. enumerate some of the human-medaited threats that act both simultaneously and synergistically against desert tortoise populations:

Habitat conversion occurs as a result of urban development, mining, waste disposal, energy development, and road construction. Habitat modification is caused by military training, off-highway vehicle use, utility corridors, livestock grazing, and the proliferation of invasive plants. … Direct losses of tortoises also occur through predation, disease, collection from the wild, and recreational killing.

Apart from climate change, which is projected to substantially reduce the historical range of the desert tortoise in the coming years, the proliferation of introduced grasses is particularly disconcerting. Such grasses tend to increase wildfire frequency in areas where wildfire is historically rare and the native flora is ill-adapted to frequent fire. This can alter plant communities in a way that favors introduced plants over plants native to the region.

Desert Tortoise (Gopherus agassizii) - photo credit: wikimedia commons

Desert Tortoise (Gopherus agassizii) – photo credit: wikimedia commons

The desert tortoise is the largest terrestrial turtle in the United States, measuring up to 15 inches long and weighing up to 15 pounds. Their carapaces are generally dull brown or gray, although those of young tortoises may have orange markings. Their limbs are stocky and elephantine, and their front legs are shovel-like and equipped with claws for digging. They reach sexual maturity between ages 15-20, generally living for at least 35 years and as many as 50-100 years.

Desert tortoises are distributed throughout the Mohave and Sonoran Deserts of southeastern United States and into the Sonaron Desert and Sinaloan foothills of northwestern Mexico. Their habitat varies widely across their range. In general, tortoises prefer sites where the soil is loamy and easy to dig as they spend much of their time in underground dens; however, they also occur in rocky foothills where shelter can be found among the rocks. In the Mohave Desert, they are commonly found in plant communities that are dominated by creosote bush (Larrea tridentata), which they use for shade and an occasional food source.

Creasote Bush (Larrea tridentata) - photo credit: wikimedia commons

Creosote Bush (Larrea tridentata) – photo credit: wikimedia commons

Recently the species known as Gopherus agassizii was determined to consist of at least two (possibly four) distinct species. Desert tortoises that occur north and west of the Colorado River have retained the scientific name G. agassizii and are commonly referred to as Agassiz’s desert tortoise. Desert tortoises occurring east of the Colorado river have been given the name G. morafkai, commonly known as Morafka’s desert tortoise. In light of this, G. agassizii may find itself uplisted to endangered, as its range has been reduced to about 30% of its former self and its southern cousins can no longer be considered a genetic reservoir.

Seeing that desert tortoises have plenty of the right foods to eat ensures their immediate survival and holds them back from the precipice of extinction. The question, “What does a desert tortoise eat?,” was what peaked my curiosity in this subject to begin with. I knew they were herbivores (for the most part), so I assumed they must have a favorite food – something that composed the majority of their diet. Finding an answer to this question led me down a rabbit hole [or should I say a tortoise hole? Some tortoise dens can extend 30 feet or more into the banks of desert dry washes.] that led me to discover the complexity of these creatures. It turns out, there is no easy answer to my initial question. What a desert tortoise eats depends on where in its expansive range it resides, what time of year it is, what plants are available in a particular year, whether or not it’s a drought year, etc.

The desert tortoise is “one of the most studied reptiles in the world,” so hundreds of observations have been made, leading to dozens of reports and studies that examine the diet of the desert tortoise; however, the results are highly variable. Due to such variability, this fact sheet from the San Diego Zoo states matter-of-factly, “an ‘average’ tortoise diet [is] hard to characterize.” But let’s try.

The desert tortoise emerges from its winter den in early spring. At the same time, annual wildflowers are also emerging, taking advantage of warming temperatures and rare soil moisture accumulated during winter precipitation. This is the desert tortoise’s preferred banquet. Because there will be little water available the rest of the year, desert tortoises hydrate themselves mainly through the plants they eat. The lush stems, leaves, and flowers of annual wildflowers provide both nutrients and the water necessary to sustain themselves throughout much of the year and aid in their growth and reproduction.

As spring turns to summer, the tortoises switch to eating herbaceous perennials and grasses. By this point, both introduced annual grasses and native perennial bunchgrasses are drying up, but tortoises are still able to extract some nutrients and moisture by eating their dry stems and leaves. Cactus pads and fruits (particularly those in the genus Opuntia) as well as young leaves of shrubs also help tortoises subsist through the long, hot summers, which are mostly spent deep in their dens away from predators and the blistering heat.

A paper published in a March 1986 issue of Herpetologica follows a group of tortoises over the period of a year and makes a number of lifestyle observations, including their diet. The authors noted that much of their diet consisted of two annual wildflowers (Camissonia munzii and Langloisia setosissima), a perennial bunchgrass (Achnatherum hymenoides), and a non-native annual grass (Bromus rubens). A paper published in a 2010 issue of Journal of Herpetology compared the nutritional quality of four plant species commonly consumed by desert tortoises: a native and non-native grass (Achnatherum hymenoides and Schismus barbatus) and a native and non-native annual forb (Malacothrix glabrata and Erodium cicutarium). They found little difference between the native and non-native species in either catagory, but determined that the forbs were significantly more nutritious than the grasses, which lead them to recommend managament practices that would increase the availability of forbs (regardless of provenance) in tortoise habitat. Numerous studies have documented the frequent consumption of introduced plant species by desert tortoises.

Redstem stork's bill (Erodium cicutarium) is an introduced species commonly consumed by desert tortoises - image credit: wikimedia commons

Redstem stork’s bill (Erodium cicutarium) is an introduced species commonly consumed by desert tortoises – image credit: wikimedia commons

For me, one of the most interesting things to learn was the variety of “non-food” items that tortoises may consume. Tortoises are often observed eating soil and rocks, and are also known to eat bones, arthropods, feces, feathers, hair, and egg shells. The rocks are thought to act as a gastrolith, aiding in digestion. The other items may help supplement minerals and nutrients the tortoises are lacking in their plant-based diet, particularly calcium which is greatly needed for growth and reproduction. Shockingly, a report that appeared in a 2007 issue of The Southern Naturalist details incidences of tortoises eating the skeletal remains of other tortoises.

Desert tortoises are an engrossing subject of study, and so much more could be said about them. For now, I leave you with this passage from Alcock’s book:

To see a tortoise with wrinkled neck and solemn eyes, moving like an animated rock, is an essential part of the experience of the desert. The removal of even a single adult extinguishes a presence that was meant to persist for years to come and snuffs out a prehistoric spark of life in a spartan environment where life, so hard-won, should be celebrated.

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Urban Botanical Art

We live on a green planet, so it is no surprise that plants frequently find their way into our artwork. They make excellent subjects after all; and arguably, botanical art can be a close second (if not a tie) to seeing the real thing.

No place is plant-themed art needed more than in urban areas. Despite trying to cram plants in wherever we can find room, our cities remain dominated by concrete, asphalt, and steel. Plants help soften the hard edges we create, and they reintroduce nature to something that otherwise seems unnatural. But there isn’t always space for plants. Botanical art is the next best thing.

When I’m not looking out for plants, I’m looking out for plant art. What follows are a few of my discoveries this past year in my hometown of Boise, Idaho and beyond. In future travels, I hope to find more botanical art in other urban areas. Meanwhile, please feel free to share with me the botanical art in your neighborhood, either through twitter, tumblr, or some other means.

Parking garage in downtown Boise, Idaho

Parking garage in downtown Boise, Idaho

My dad's mural in downtown Mountain Home, Idaho

Mural by Stephen Murphy (my dad!) in downtown Mountain Home, Idaho

Mural in Freak Alley in downtown Boise, Idaho

Freak Alley Gallery in downtown Boise, Idaho

Mural in Freak Alley in downtown Boise, Idaho

Freak Alley Gallery in downtown Boise, Idaho

Agoseris sculpture at Foothills Learning Center in Boise, Idaho

Aero Agoseris sculpture (Agoseris glauca) at Foothills Learning Center in Boise, Idaho

Stop sign in Sunset Neighborhood in Boise, Idaho

Stop sign in Boise’s Sunset Neighborhood

Stop sign in Sunset Neighborhood in Boise, Idaho

Stop sign in Boise’s Sunset Neighborhood

Utility boxes in downtown Boise, Idaho

Utility boxes in downtown Boise, Idaho

Utility box in Boise, Idaho

Utility box in downtown Boise, Idaho

Influence of a Passion

This is a guest post by Samuel Malley.

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One of the most fascinating parts of plant interest is learning about those who have contributed to it as a whole. It has inspired great men and women who made it what it is today – from the Greek Theophrastrus, regarded as the father of botany through to Margaret Rebecca Dickinson who would bring these plants to life through illustrations. To learn about their lives is an absolute joy, knowing your passion has birthed these amazing people.

Take Carl Linnaeus, for example, a man who invented a method to name plants according to their genus, species, and so forth. We use this commonly today as it has become his legacy that impacts every botanist, gardener, and horticulturist as well as many others in the world. As the Roman naturalist Pliny the Elder would say “fortune favours the brave.” This quote would certainly apply to many. The dream to travel to new far away lands and discover new plant species would indeed inspire those willing to be brave and be rewarded in return. Even now in this day and age people are still imagining and travelling to see what else is out there. And who knows, a plant could be discovered soon that pushes the boundaries of what we think and know.

One of the first botanists I came across just as my obsession was starting was Luca Ghini. Born in 1490, he created the first botanical garden in Pisa, Italy. Ghini also created a technique of drying and pressing plants, eventually being recorded with having the first herbarium. This supposedly contained around three hundred specimens.

To me Luca is one of my personal heroes – someone who’s genius shaped the modern plant world. What a privilege it must have been to be the first to have stepped into the Pisa Garden or to be in the company of Luca as he added a new leaf to his collection. He passed away in 1556, and like every great botanist he left a legacy. Ghini is still here, alive through his garden and his drying technique. To the man himself, if I could go back in time, the two words that I would say to him would be, “Thank you.”

Pisa Botanical Garden - photo credit: Chris / flickr

Pisa Botanical Garden – photo credit: Chris/Flickr

The future ahead in plant interest is a very bright one, awaiting more great people to add to the rich, fascinating history it has to offer full of eye opening men and women.

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Samuel Malley is a horticulture student in the United Kingdom. He is an aspiring botanist and is also interested in creating unique garden sculptures. 

How a Plant Could Just Kill a Man, part two

Plants falling on people was a major theme in the Caustic Soda podcast Killer Plants episode, which is why part one of this two part series was devoted entirely to the subject. Yet, in the process of discussing death by falling branches and fruits, the hosts also mentioned at least three other highly dangerous and potentially deadly plants: ongaonga, gympie gympie, and the little apple of death. Those plants are featured here.

The nettle family, Urticaceae, includes a number of species that are best admired from a distance. Several genera (out of around 53 total) in this family are equipped with stinging hairs – sharp protrusions on leaves and stems that contain a variety of toxic compounds. Contact with these plants is ill-advised. Reactions vary from mild to extreme depending on the extent of the contact and the species in question. Two of the plant species mentioned by the hosts of Caustic Soda are members of this family – ongaonga (Urtica ferox) and gympie gympie (Dendrocnide moroides) – both of which are on the extreme side of the scale.

Urtica ferox is a New Zealand endemic that is commonly found in coastal and lowland areas as well as forest edges and shrublands. It is a shrub that reaches up to three meters tall and often occurs in dense thickets. The margins and midribs of its leaves are adorned with stiff hairs that are just a few millimeters long and poised to inject toxic compounds including histamine and acetylcholine upon contact. The “sting” is painful and can cause a variety of reactions including itching, inflammation, difficulty breathing, paralysis, blurred vision, and convulsions. Symptoms can last for several days, and neurological disorders occur in extreme cases.

Ongaonga has been blamed for killing several animals, including dogs and horses, but is charged with only one human death. In 1961, two hikers ventured into a patch of the stinging nettles. Shortly after contact they had trouble walking, breathing, and seeing. One of the men died a few hours later; the other recovered.

Ongaonga (Urtica ferox) - photo credit: www.eol.org

Ongaonga (Urtica ferox) – photo credit: www.eol.org

Several species in the nettle family can be found in Australia, one of which is particularly dangerous. Dendrocnide moroides, commonly known as stinging tree or suicide plant, is an early successional species, colonizing disturbed sites and sunlit gaps in the rainforest canopy. It grows to about three meters tall and has large heart-shaped leaves with sawtooth margins. All aboveground parts of the plant are covered in silicon hairs that are packed with a highly potent neurotoxin. The hairs detach easily from the plant and embed themselves in the skin of its victims. The “sting” is extremely painful and can last anywhere from days to months, possibly even returning from time to time years after contact. A rash, swelling, and itching sensation accompany the intense pain.

Following an encounter with the stinging tree, the “stingers” should be removed from the skin with a hair removal strip or some other sticky material, taking care not to break off the embedded tips. The affected area can be treated with diluted hydrochloric acid (1:10 by volume) to reduce the pain. Live plants are not the only ones to be wary of, as even old herbarium specimens have been said to sting those that handle them. Touching the plant isn’t even necessary, as the hairs easily dislodge from the plant in the wind and can be breathed in. One researcher reports developing a severe allergic reaction to the plant after working around it for several years and was advised by a doctor to abandon her research.

The spurge family, Euphorbiaceae, has many toxic plants among its ranks, including a species that Guiness World Records has awarded the world’s most dangerous tree. Commonly known as manchineel or beach apple, Hippomane mancinella demands respect, as a highly toxic latex sap is found throughout the entire plant. Just standing near it can result in painful blistering of the skin. Manchineel occurs along shorelines and in coastal woodlands and swamps in Central America and the West Indies, including southern Florida and the Florida Keys. It is a deciduous tree that grows to about fifteen meters tall, has thick grey bark, and glossy, elliptical leaves. Its fruits look like yellow-green crabapples and are sweet smelling and initially sweet tasting, that is until the burning and swelling starts followed by severe gastroenteritis.

Manchineel tree a.k.a. little apple of death (Hippomane mancinella) - photo credit: www.eol.org

Manchineel tree a.k.a. little apple of death (Hippomane mancinella) – photo credit: www.eol.org

Interaction with manchineel is inadvisable. The thick, milky sap seeps out of leaves, branches, bark, and fruits and causes intense blistering of the skin and temporary blindness if it gets near the eyes. During rainstorms, the sap becomes incorporated in raindrops and can drip or splash onto unwitting bystanders. Smoke from burning trees can also irritate the skin and eyes, and inhalation of the sawdust can result in bronchitis, laryngitis, and other respiratory issues. Modern history does not include reports of human fatalities resulting from eating the little apples of death, but descriptions offered by those who have consumed it confirm that it is an incredibly unpleasant experience.

Related Posts:

How a Plant Could Just Kill a Man, part one

Plants have killed plenty of people. When plants are implicated in the death of a human, we typically think of plant poisonings. Rightly so since their are a slew of poisonous plants with the potential to kill. However, oftentimes plants kill (or seriously injure) people without employing toxic substances. One of the best examples of this is falling plant parts. Gravity couples with sheer coincidence and/or human error, and tragedy ensues. In an episode entitled Killer Plants of the now defunct podcast, Caustic Soda, the hosts present some of these distressing scenarios. What follows is a summary of the plants that made their list.

Branches falling from trees, whether dead or alive, can cause some serious damage. Trees in the genus Eucalyptus, commonly known as gum trees, are one group to be particularly wary of. There are more than 700 species of Eucalyptus, most of which occur in Australia. Not all are large trees, but those that are can be massive, reaching from 100 to 200 feet and taller. Eucalyptus trees regularly shed branches, often unexpectedly, leading to serious injury or death to anyone who may find themselves on the ground below. Shedding branches is likely a strategy for conserving water during hot, dry summers, and it is common enough that Australian parks departments issue safety advisories to avoid parking or camping below the trees. Even arborists don’t take their chances with these unpredictable trees.

Red River Gum Tree Eucalyptus camaldulensis - photo credit: wikimedia commons

River red gum (Eucalyptus camaldulensis) – photo credit: wikimedia commons

Of course, eucalyptus trees are not the only trees that drop their branches without warning. A falling branch in Yosemite National Park claimed two victims last summer, for example; and falling branches have claimed the lives of a great deal of forest workers, wildland firefighters, and other forest visitors. This happens frequently enough that the branches in question have been given the ominous name widowmakers, and the U.S. Department of Labor lists them as one of many “potential hazards” in the logging industry. What are the chances of being killed by a falling tree? The Ranger’s Blog set out to answer that question and, to set your mind at ease, determined that the chances are pretty slim.

What about other falling plants? Saguaro cactus, for example. Carnegiea gigantea is a tree-like, columnar cactus native to the Sonoran Desert. It is a very slow growing and long-lived species that generally reaches around 40 feet tall but can potentially grow much taller. Saguaros are considered tree-like for their tall stature and branching habit, although not all saguaros develop branches. Some saguaro branches (or “arms”) can be quite large and considerably heavy. In 1982, an Arizona man discovered this when he and a friend were out shooting saguaros. Stupidly, the man repeatedly shot at the arm of an enormous cactus. Ultimately the arm split off and landed on the man, crushing him to death. Of course, saguaros don’t have to be shot at to fall on you. Another Arizona man was fixing a water leak in a Yuma subdivision when a sixteen foot tall saguaro toppled over on him. The man was crushed but lived to tell about it.

Saguaro cactus (Carnegiea gigantea) - photo credit: wikimedia commons

Saguaro cactus (Carnegiea gigantea) – photo credit: wikimedia commons

Palm trees drop things on people, too. One tragic example involves a man in Los Angeles standing below a Canary Island date palm (Phoenix canariensis) waiting for a ride to a funeral. The 2000 pound crown of the palm tree split and fell, pinning the man to the ground. Bystanders were unable to remove the crown, and the man died.

The coconut palm (Cocos nucifera) has an additional deadly weapon – its fruit. While the number of deaths by coconut are often exaggerated, they do occasionally occur. Injuries by coconut are more frequent, so precaution around the trees should be taken. After all, coconut palms can reach heights of 80 feet or more, and mature coconuts can weigh more than three pounds (considerably more when they are wet). A falling coconut is something to be mindful of, an observation that led Dr. Peter Barss to study coconut related injuries in Papa New Guinea over a period of 4 years. His research was published in 1984 in the Journal of Trauma and was later taken out of context and used to make the claim that coconuts kill significantly more people per year than sharks. Publicity spawned by this urban myth helped Barss earn an Ig Noble Prize in 2001. Concerns about coconut related injuries also led officials in India to order the removal of coconut palms around the Gandhi Museum in preparations for President Barack Obama’s 2010 visit.

Back in Australia, the towering bunya pine (Araucaria bidwillii) has its equivalent to the coconut in its massive cone. Measuring around a foot long and weighing in at 20+ pounds, these cones make living near bunya pines an act that is “not for the faint hearted.” When the cones are falling, they warrant warnings from the Australian government to keep away from these 90 foot tall trees. This harrowing feature puts bunya pines on a list of infamous plants in Australia with the potential to kill.

Bunya pine cone (Araucaria bidwillii) - photo credit: www.eol.org

Seed cone of bunya pine (Araucaria bidwillii) – photo credit: www.eol.org

Tomato vs. Dodder, or When Parasitic Plants Attack

At all points in their lives, plants are faced with a variety of potential attackers. Pathogenic organisms like fungi, bacteria, and viruses threaten to infect them with diseases. Herbivores from all walks of life swoop in to devour them. For this reason, plants have developed numerous mechanisms to defend themselves against threats both organismal and environmental. But what if the attacker is a fellow plant? Plants parasitizing other plants? It sounds egregious, but it’s a real thing. And since it’s been going on for thousands of years, certain plants have developed defenses against even this particular threat.

Species of parasitic plants number in the thousands, spanning more than 20 different plant families. One well known group of parasitic plants is in the genus Cuscuta, commonly known as dodder. There are about 200 species of dodder located throughout the world, with the largest concentrations found in tropical and subtropical areas. Dodders generally have thread-like, yellow to orange, leafless stems. They are almost entirely non-photosynthetic and rely on their host plants for water and nutrients. Their tiny seeds can lie dormant in the soil for a decade or more. After germination, dodders have only a few days to find host plants to wrap themselves around, after which their rudimentary roots wither up. Once they find suitable plants, dodders form adventitious roots with haustoria that grow into the stems of their host plants and facilitate uptake of water and nutrients from their vascular tissues.

A mass of dodder (Cuscuta sp.) - photo credit: wikimedia commons

A mass of dodder (Cuscuta sp.) – photo credit: wikimedia commons

Some plants are able to fend off dodder. One such instance is the cultivated tomato (Solanum lycopersicum) and its resistance to the dodder species, Cuscuta reflexa. Researchers in Germany were able to determine one of the mechanisms tomato plants use to deter dodder; their findings were published in a July 2016 issue of Science. The researchers hypothesized that S. lycopersicum was employing a similar tactic to that of a microbial invasion. That is, an immune response is triggered when a specialized protein known as a pattern recognition receptor (PRP) reacts with a molecule produced by the invader known as a microbe-associated molecular pattern (MAMP). A series of experiments led the researchers to determine that this was, in fact, the case.

The MAMP was given the name Cuscuta factor and was found “present in all parts of C. reflexa, including shoot tips, stems, haustoria, and, at lower levels, in flowers.” The PRP in the tomato plant, which was given the name Cuscuta receptor 1 (or CuRe 1), reacts with the Cuscuta factor, triggering a response that prohibits C. reflexa access to its vascular tissues. Starved for nutrients, the dodder perishes. When the gene that codes for CuRe 1 was inserted into the DNA of Solanum pennellii (a wild relative of the cultivated tomato) and Nicotiana benthamiana (a relative of tobacco and a species in the same family as tomato), these plants “exhibited increased resistance to C. reflexa infestation.” Because these transgenic lines did not exhibit full resitance to the dodder attack, the researchers concluded that “immunity against C. reflexa in tomato may be a process with layers additional to CuRe 1.”

photo credit: wikimedia commons

photo credit: wikimedia commons

A slew of crop plants are vulnerable to dodder and other parasitic plants, so determining the mechanisms behind resistance to parasitic plant attacks is important, especially since such infestations are so difficult to control, have the potential to cause great economic damage, and are also a means by which pathogens are spread. It is possible that equivalents to CuRe 1 exist in other plants that exhibit resistance to parasitic plants, along with other yet to be discovered mechanisms involved in such resistance, so further studies are necessary. Discoveries like this not only help us make improvements to the plants we depend on for food, but also give us a greater understanding about plant physiology, evolutionary ecology, and the remarkable ways that plants associate with one another.

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Maize Anatomy and the Anatomy of a Maze

Commonly known as corn throughout much of North America, maize is a distinctive emblem of the harvest season. It is one of the most economically important crops in the world (the third most important cereal after rice and wheat) and has scads of uses from food to feed to fuel. The story of its domestication serves as a symbol of human ingenuity, and its plasticity in both form and utility is a remarkable example of why plants are so incredible.

The genus Zea is in the grass family (Poaceae) and consists of five species: Z. diploperennis, Z. perennis, Z. luxurians, Z. nicaraguensis, and Z. mays. Maize is the common name of Zea mays subsp. mays, which is one of four Z. mays subspecies and the only domesticated taxon in the genus. All other taxa are commonly and collectively referred to as teosintes.

The domestication of maize, apart from being an impressive feat, has long been a topic of research and a challenging story to tease apart. The current understanding is that maize was first domesticated around 9000 years ago in the Balsas River valley in southern Mexico, the main progenitor being Zea mays subsp. parviglumis. It is astonishing how drastically different in appearance teosintes are from modern day maize, but it also explains why determining the crop wild relative of maize was so difficult.

Teosinte, teosinte-maize hybrid, and maize - photo credit: wikimedia commons

Teosinte, teosinte-maize hybrid, and maize – photo credit: wikimedia commons

Teosintes and maize both have tall central stalks; however, teosintes generally have multiple lateral branches which give them a more shrubby appearance. In teosinte, each of the lateral branches and the central stalk terminate in a cluster of male flowers; female flowers are produced at the nodes along the lateral branches. In maize, male flowers are borne at the top of the central stalk, and lateral branches are replaced by short stems that terminate in female flowers. This is where the ears develop.

Ears – or clusters of fruits – are blatantly different between teosintes and maize. To start with, teosinte produces a mere 5 to 12 fruits along a short, narrow cob (flower stalk). The fruits are angular and surrounded in a hard casing. Maize cobs are considerably larger both in length and girth and are covered in as many as 500 or more fruits (or kernels), which are generally more rounded and have a softer casing. They also remain on the cob when they are ripe, compared to teosinte ears, which shatter.

Evolutionary biologist, Sean B. Carroll, writes in a New York Times article about the amazing task of “transform[ing] a grass with many inconvenient, unwanted features into a high-yielding, easily harvested food crop.” These “early cultivators had to notice among their stands of plants variants in which the nutritious kernels were at least partially exposed, or whose ears held together better, or that had more rows of kernels, and they had to selectively breed them.” Carroll explains that this “initial domestication process which produced the basic maize form” would have taken several hundred to a few thousand years. The maize that we know and love today is a much different plant than its ancestors, and it is still undergoing regular selection for traits that we find desirable.

Female inflorescence (or "ear") of Zea mays subsp. mays - photo credit: wikimedia commons

Female inflorescence (or “ear”) of Zea mays subsp. mays – photo credit: wikimedia commons

To better understand and appreciate this process, it helps to have a basic grasp of maize anatomy. Maize is an impressive grass in that it regularly reaches from 6 to 10 feet tall and sometimes much taller. It is shallow rooted, but is held up by prop or brace roots – adventitious roots that emerge near the base of the main stalk. The stalk is divided into sections called internodes, and at each node a leaf forms. Leaf sheaths wrap around the entirety of the stalk, and leaf blades are long, broad, and alternately arranged. Each leaf has a prominent midrib. The stalk terminates in a many-branched inflorescence called a tassel.

Maize Anatomy 101 - image credit: Canadian Goverment

Maize Anatomy 101 – image credit: Canadian Government

Maize is monoecious, which means that it has separate male and female flowers that occur on the same plant. The tassel is where the male flowers are located. A series of spikelets occur along both the central branch and the lateral branches of the tassel. A spikelet consists of a pair of bracts called glumes, upper and lower lemmas and paleas (which are also bracts), and two simple florets composed of prominent stamens. The tassel produces and sheds tens of thousands of pollen grains which are dispersed by wind and gravity to the female inflorescences below and to neighboring plants.

Female inflorescences (ears) occur at the top of short stems that originate from leaf axils in the midsection of the stalk. Leaves that develop along this reduced stem wrap around the ears forming the husk. Spikelets form in rows along the flower stalk (cob) within the husk. The florets of these spikelets produce long styles that extend beyond the top of the husk. This cluster of styles is known as the silk. When pollen grains land on silk stigmas, pollen tubes grow down the entire length of the silks to reach the embryo sac. Successful fertilization produces a kernel.

The kernel – or fruit – is known botanically as a caryopsis, which is the standard fruit type of the grass family. Because the fruit wall and seed are fused together so tightly, maize kernels are commonly referred to as seeds. The entire plant can be used to produce feed for animals, but it is the kernel that is generally consumed (in innumerable ways) by humans.

There is so much more to be said about maize. It’s a lot to take in. Rather than delve too much further at this point, let’s explore one of the other ways that maize is used by humans to create something that has become another feature of the fall season – the corn maze.

Entering the corn maze at The Farmstead in Meridian, Idaho

Exploring the corn maze at The Farmstead in Meridian, Idaho

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Bat Pollinated Flowers of a Mexican Columnar Cactus

Pollination syndromes – suites of floral traits used to determine potential pollinators and routes of pollination – have been informative in studying plant-pollinator interactions, but are generally too simplistic to tell the full story. Most flowering plants are generalists when it comes to pollinators, whereas pollination syndromes imply specialization. Not all pollinators are created equal though, and some may be more effective at pollinating particular plants than others. In fact, occasionally pollination syndromes ring true and a predicted plant-pollinator combination turns out to be the most effective and reliable interaction.

According to a study published in American Journal of Botany by Ibarra-Cerdeña, et al., Stenocereus queretaroensis, a species of columnar cactus endemic to western Mexico, adheres to this scenario. Stenocereus is a genus in a group of columnar and tree-like cacti called the Pachycereeae tribe. Cactus in this group are generally bat pollinated; however, their flowers are typically visited by various species of birds and insects as well, and in some cases, bats are not the primary pollinator. In their introduction, the authors note that specialization appears to be more common in tropical latitudes, and chiropterophilic (bat pollinated) columnar cacti that occur in temperate regions can be comparatively more generalized. This is because “extratropical chiropterophilic cacti appear to be faced with unpredictable seasonal year-to-year variation in pollinators,” while “cacti in tropical regions” experience “highly reliable seasonal availability of nectar-feeding bats, thereby leading to a temporally stable pollination system.”

Stenocereus queretaroensis is a massive cactus, reaching up to ten meters tall. Several vertical stems rise from a short, stocky, central trunk. Each stem has up to eight distinctive ribs and averages around 15 centimeters in diameter. Groupings of white to grey spines up to four centimeters long appear along the ribs. Flowers are light-colored, around 10 to 14 centimeters in length, and occur along the upper half of the stems, extended well beyond the spines. Flowers open at night – producing abundant nectar – and close by the afternoon the following day. Floral characteristics led the authors of this study to predict bats to be the main pollinator, and they set up a series of experiments to test this.

Stenocereus queretaroensis - photo credit: wikimedia commons

Stenocereus queretaroensis – photo credit: wikimedia commons

Part of their experiment consisted of five treatments involving 130 flowers on 75 plants. One group of flowers was bagged and allowed to self-pollinate naturally, while another group was bagged and self-pollinated manually. A third group was left exposed during the night but bagged in the morning, while a fourth group was bagged during the night and exposed during the daytime. The final group was left alone. For each of these five treatments, aborted flowers and mature fruits were counted and seed set was determined. Nectar samples were taken from a separate group of flowers at two hour intervals from 8:00 PM to 8:00 AM, after which no nectar was produced. A camera was also used to document floral visits. Visits were deemed “legitimate” when the “visitor’s body came in contact with anthers and/or stigma” and “illegitimate” when “no contact with anthers or stigma” was made.

The researchers found S. queretaroensis to be “incapable of self-pollination,” as no fruit set occurred for the first two treatments. The control group and the nocturnally exposed group had nearly identical results, producing significantly more fruits with greater seed set compared to the nocturnally bagged group. During the day, flowers were visited by four species of birds (two hummingbirds, a woodpecker, and an oriole) and several species of bees (mainly honey bees). During the night, apart from illegitimate visits from a nectar robbing hawkmoth, one species of bat was the dominant floral visitor, and the majority (93.8%) of the visits were legitimate. This bat species was Leptonycteris curasoae, the southern long-nosed bat.

Leptonycteris curasoae - photo credit: wikimedia commons

Leptonycteris curasoae – photo credit: wikimedia commons

The abundance of nectar-feeding bats was monitored in the study area over a four year period, and L. curasoae was by far the most abundant species throughout the study period. Nectar produced in the flowers of S. queretaroensis was at its maximum around midnight, which seemed to correlate with observations of bat visits. Even though daytime visitors appeared to contribute to fruit and seed set, the nocturnal treatment produced significantly more fruit with significantly higher seed set, suggesting that bats are the more efficient pollinator. Insects visiting during the daytime, when nectar was decreasingly available, were most likely robbing pollen.

The authors acknowledge that for most plant species, “a wide array of taxonomically diverse fauna such as insects, birds, and mammals usually serve as potential pollinators,” and that “generalized pollination systems are more frequent than specialized ones.” However, in this case, “a close association between L. curasoae and S. queretaroensis [suggests] that the chiropterophilic syndrome is still a useful model.”

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Bats As Pollinators – An Introduction to Chiropterophily

Most plants that rely on animals to assist in pollination look to insects. In general, insects are abundant, easy to please, and efficient at transferring pollen. Because insect pollination is such a common scenario, it is easy to overlook pollination that is carried out by vertebrates. Birds are the most prominent pollinator among vertebrates, but mammals participate, too. The most common mammal pollinator is the bat.

About a fifth of all mammal species on the planet are bats, with species estimates numbering in the 1200-1300 range. Bats are the only mammals that can truly fly. They are not blind, nor are they flying rodents, and they are not going to suck your blood (except in very rare cases!). Most bats eat insects, but a small, significant group of them are nectarivorous. Their main food source is the nectar produced within flowers. In the process of feeding, these bats pollinate plants.

Out of 18 families in the order Chiroptera, only two include species with morphologies that set them apart as nectar-feeders. The family Pteropodidae, known commonly as Old World fruit bats or flying foxes, occurs in tropical and subtropical regions of Africa, Asia, Australia, Papa New Guinea, and the Pacific Islands. The family Phyllostomidae, known commonly as American leaf-nosed bats, occurs in tropical and subtropical regions of the Americas. For simplicity’s sake, the former are referred to as Old World bats, and the latter as New World bats. While both groups are similar in that they consist of species that feed on nectar, they are only distantly related, and thus the nectar feeding species in these families have distinct behavioral and morphological differences.

Grey headed flying fox photo credit: wikimedia commons

Grey headed flying fox (Pteropus poliocephalus), a floral visiting bat from Australia (photo credit: wikimedia commons)

More than 500 species of plants, spanning 67 plant families, are pollinated by bats. This pollination syndrome is known as chiropterophily. In general, flowers that use this approach tend to be white or dull in color, open at night, rich with nectar, and musty or rotten smelling. They are generally tubular, cup shaped, or otherwise radially symmetrical and are often suspended atop tall stalks or prominently located on branches or trunks. In a review published in Annals of Botany, Theodore Fleming, et al. state “flower placement away from foliage and nocturnal anthesis [blooming] are the unifying features of the bat pollination syndrome,” while all other characteristics are highly variable among species. The family Fabaceae contains the highest number of bat-pollinated genera. Cactaceae, Malvaceae, and Bignoniaceae follow closely behind.

The characteristics of bat pollinated flowers vary widely partly because the bats that visit them are so diverse. Between the two bat families there are similarities in their nectar-feeding species, including an elongated rostrum, teeth that are smaller in number and size, and a long tongue with hair-like projections on the tip. Apart from that, New World bats are much smaller than Old World bats, and their rostrums and tongues are much longer relative to the size of their bodies. New World bats have the ability to hover in front of flowers, while Old World bats land on flowers to feed. Old World bats do not have the ability to use echolocation to spot flowers, while New World bats do. Fleming, et al. conclude, “because of these differences, we might expect plants visited by specialized nectar-feeding [New World bats] to produce smaller flowers with smaller nectar volumes per flower than those visited by their [Old World bat] counterparts.”

Pollination by bats is a relatively new phenomenon, evolutionarily speaking. Flowers that are currently pollinated by bats most likely evolved from flowers that were once pollinated by insects. Some may have evolved from flowers that were previously bird pollinated. The question is, why adopt this strategy? Flowers that are bat pollinated are “expensive” to make. They are typically much bigger than insect pollinated flowers, and they contain large amounts of pollen and abundant, nutrient-rich nectar. Due to resource constraints, many plants are restricted from developing such flowers, but those that do may find themselves at an advantage with bats as their pollinator. For one, hairy bat bodies collect profuse numbers of pollen grains, which are widely distributed as they visit numerous flowers throughout the night. In this way, bats can be excellent outcrossers. They also travel long distances, which means they can move pollen from one population of plants to an otherwise isolated neighboring population. This serves to maintain healthy genetic diversity among populations, something that is increasingly important as plant populations become fragmented due to human activity.

Pollinating bats are also economically important to humans, as several plants that are harvested for their fruits, fibers, or timber rely on bats for pollination. For example, bat pollinated Eucalyptus species are felled for timber in Australia, and the fruits of Durio zibethinus in Southeast Asia form after flowers are first pollinated by bats. Also, the wild relatives of bananas (Musa spp.) are bat pollinated, as is the plant used for making tequila (Agave tequilana).

Durio sp. (photo credit: wikimedia commons)

The flowers of durian (Durio sp.), trees native to Southeast Asia, are pollinated by bats (photo credit: wikimedia commons)

There is still much to learn about nectarivorous bats and the flowers they visit. It is clear that hundreds of species are using bats to move their pollen, but the process of adopting this strategy and the advantages of doing so remain ripe for discovery. Each bat-plant relationship has its own story to tell. For now, here is a fun video about the bat that pollinates Agave tequilana: