The Stench of Death, brought to you by the Forests of Sumatra

(Via: The Parasitic Plant Connection)

Common Name: Giant Rafflesia

A.K.A.: Rafflesia arnoldii

Vital Stats:

  • One of about 28 species of Rafflesia, all parasites native to southeast Asia
  • Dioecious: produces male and female flowers on separate plants
  • Flowers last only a few days

Found: In the rainforests of Sumatra, Western Indonesia

It Does What?!

In my very first post here on Questionable Evolution, I discussed the Titan Arum, a.k.a. Corpse Plant, known for its pungent aroma and generally phallic appearance. This rare oddity is confined to the ever-shrinking rainforests of the western Indonesian island of Sumatra. Now meet its neighbour and fellow rotting flesh imitator, the Giant Rafflesia. Like the Titan Arum, this species is found only in the Sumatran rainforest and uses its odour to attract carrion flies for pollination. (With all the plants pretending to be dead animals on this island, it’s a wonder the flies ever actually find themselves any real carcasses.)

How big?  THAT big.
(With Mr. Troy Davis, Via: The Parasitic Plant Connection)

Rafflesia’s claim to fame in the plant world is that it produces the largest flower on Earth. A single bloom from Rafflesia arnoldii can reach a diameter of 1m (3.3’) and a mass of up to 7kg (15lbs.). In other words, one flower weighs about as much as your overweight cat. Impressive, sure, but what’s more interesting about this plant is that the flower’s the only part of it you’re ever likely to see.

Much like dodder, rafflesia is a holoparasite, depending entirely on a host plant (in this case, a vine of genus Tetrastigma, part of the grape family) for its water and nutrients. Unlike dodder, however, rafflesia doesn’t grow up and over its victim, eventually smothering it- no, this plant grows inside its host. Over the course of its evolution, the leaves, roots, and stems of rafflesia have been reduced to nothing but miniscule threads that grow, fungus-like, through the intercellular spaces of another plant, absorbing whatever they require. The giant flower arises directly from the roots or stem of the host vine, pushed out through the host’s tissues. Think chestbursters from Alien. Beyond the juvenile phase when a new seedling searches for its host, this is the only part of rafflesia that will ever see the light of day.

Flowering Time!!

Interestingly, botanists have found that rafflesia’s giant flowers evolved over a very short period of time (relatively speaking), with flower diameter increases of, on average, 20cm per million years. Blindingly fast, as plant evolution goes. The reason for this, they speculate, may have been a preference on the part of certain carrion flies to feed on larger animal carcasses. The range of flower sizes seen in different species of genus Rafflesia probably functions to attract different sets of fly species with varying tastes – some want wee little dead mice, some want dead rhinoceros, judging from the size of these things.

Plants: give ‘em a few million years, and they can mimic almost anything.

Says Who?

  • Barkman et al. (2008) Current Biology 18: 1508-1513
  • Beaman et al. (1988) American Journal of Botany 75(8): 1148-1162
  • Patifino et al. (2002) New Phytologist 154: 429-437

EVOLUTION TAG TEAM, Part 3: Coral Polyps & the Garden Within

The third in an ongoing series of biology’s greatest duos. (Check out Parts One and Two)

(Via: Wikimedia Commons)

Common Name: Coral Polyps

  • A.K.A.: Class Anthozoa, Subclass Hexacorallia

Common Name: Coral Algae

  • A.K.A.: Genus Symbiodinium

Vital Stats:

  • Polyps grow to a length of only a few centimetres, depending on species
  • Coral can grow outward at a rate of up to 10cm (4”) per year
  • The Great Barrier Reef stretches over 2000km (1243 mi) and can be seen from space

Found: Various coastal areas; largest reefs surrounding Australia, Oceania, and the Caribbean

It Does What?!

If you’ve ever been told that coral reefs are alive, then looked at one and felt a bit sceptical that this chuck of colourful rock could be a living thing… well, good for you, because you’re actually mostly right. The vast majority of the volume of a coral reef is, in fact, nonliving inorganic mineral (calcium carbonate, specifically). The amazing thing about coral isn’t so much what it’s made of, but what’s going on on the surface. You see, that oddly-shaped, porous rock is actually a communal exoskeleton produced and excreted over time by hundreds of thousands of polyps living in the tiny, cup-shaped depressions on the surface.

“Breaded, with a side of chips, please.”
(Via: Wikimedia Commons)

Looking like tiny jellyfish (and belonging to the same phylum), the polyps hide in the stony sanctuary they’ve made, letting only their tentacles project. These tentacles are tipped with stinging cells which can inject a powerful venom into any prey foolish enough to swim within reach. This prey can range in size from microscopic plankton to small fish. That’s right, coral eats fish. Watch where you stick your toes.

So where does the ‘duo’ part come in? Despite their ability to snatch passing sea creatures and eat them, coral polyps actually get only a small part of their caloric intake this way. Impressively, these guys managed to find a diet that requires even less effort than just reaching out and grabbing stuff. Who needs movement when you can just photosynthesize, like plants do? The polyps have developed a symbiosis with a type of single-celled alga (called zooxanthellae) that allows them to do just that.

The algae start out as free-living cells drifting through the water. They are eaten by the coral polyp, but instead of being digested, they are able to enter the cells lining its digestive tract. Since the polyps are transparent to begin with, all they have to do is expose their bodies to sunlight in order to allow the algae to produce sugars by photosynthesis (this is why reefs form in relatively shallow waters). The majority of the sugars made by the symbiont are then absorbed by the polyp.

And what do the algae get out of this arrangement? A couple of things. First, they get a safe place to live, and won’t get eaten by something that can digest them. Second, they get nutrients, in the form of carbon dioxide and nitrogen compounds, both natural waste products of the polyp’s metabolism. Still, sometimes as much as 30% of the cells in a polyp are algal cells, and this puts a stain on the host’s physiology.

“I’ve just got a lot going on right now.”
(Via: Wikimedia Commons)

Maybe you’ve heard of “coral bleaching” as one of the symptoms of pollution around reefs. Bleaching happens when additional stresses (like pollution) get to be a bit too much for the polyps to handle. They can’t change the water purity, so instead, they offload the stressor they can control- the algae. Getting rid of the photosynthetic cells also gets rid of much of the characteristic colour of the reef, hence the term ‘bleaching’. In the short term, this is a smart move. It increases the polyp’s chance of survival during brief crises, and new algae can always be taken on when the host is ready. The real problems start when the environmental stress persists, and the polyp never takes on new algae. Eventually, it can’t sustain itself and dies, as those in a tenth of the world’s reefs already have. At least there’s still hope for these areas; if conditions improve, new colonies can be formed using the old reef as a foundation. The Great Barrier Reef, for example, is considered to be between 6000 and 8000 years old. However, the modern structure has developed atop an older, dead reef system, thought to be over half a million years old. Time enough for us to clean up our act, maybe.

[Fun Fact: Coral polyps only reproduce sexually to start new colonies. Within a single piece of coral, all the polyps are genetically identical clones, produced by polyps dividing in half and then re-growing their lost tissues.]

Says Who?

  • CoRIS- Coral Reef Information System
  • Fransolet et al. (2012) Journal of Experimental Marine Biology and Ecology 420-421:1-7
  • Piper (2007) Extraordinary Animals. Greenwood Press: Westport, Connecticut.
  • Wooldridge (2010) BioEssays 32(7):615-625

    The little-known “Lady Gaga Coral”
    (Via: Wikimedia Commons)

The Plant That Time Forgot (Welwitschia mirabilis)

(Via: Wikimedia Commons)

Common Name: Welwitschia mirabilis

A.K.A.: Welwitschia

Vital Stats:

  • Welwitschia is a gymnosperm, like pines or firs, and thus reproduces via male and female cones
  • Considered a “living fossil”
  • Named after one of its discoverers, Austrian botanist Friedrich Welwitsch
  • In mature specimens, the woody stem can grow up to one metre (3.3’) across

Found: In the Namib desert, along the west coast of Namibia and Angola

It Does What?!

Restricted to a tiny, arid swath of African desert, Welwitschia mirabilis represents the last remaining species of a very unusual lineage of plants. Close relatives met with extinction over the aeons, while welwitschia, tucked away in its remote and harsh desert range with little competition, just kept going. The fact that the species is alone, not just in its genus, but also in its family and order (the two ranks above genus in plant systematics), speaks to just how distantly related to any other living plant it is. For the sake of comparison, the Rosales, the order to which roses, apples, and pears belong, contains around 7700 species in 9 families and 260 genera. So original and captivating is welwitschia among plants that it has been the subject of more than 250 scientific articles since it was first described in 1863.

A mere infant. But probably still older than you are.
(Via: Lizworld.com)

So what makes this thing so weird? Well, plants typically have what’s called an apical meristem at the tips of their stems and/or branches. You can think of this as a clump of stem cells that keeps dividing, throwing off new leaves and buds in its wake. If you cut off the apical meristem, the plant must either develop a new one elsewhere, or stop producing new tissue.

In welwitschia, this isn’t the case. At the beginning of the plant’s life, the apical meristem produces just two leaves, and then dies. The plant will never grow another leaf, which is much more surprising when you consider that it may well live for more than a thousand years. How do you get through a millennium with only two leaves?! The answer is, these aren’t ordinary leaves. Uniquely, welwitschia’s two strap-like leaves have a band of meristematic tissue built into their base, which means they can continue to elongate outward indefinitely. The leaves will continue to grow at a rate of around half a millimetre (0.02”) per day for as long as the plant lives. If you’re thinking that this must mean leaves that are several hundred metres long, unfortunately, no, they aren’t. The leaves are abraded away by sand storms and eaten by passing animals. Even in the best case scenario, the cells at the leaf tips have a maximum lifetime of about ten years (still pretty good for a leaf…). What’s more, the leaves tend to get frayed and split over time, and end up looking like a lot more than just two leaves. Despite all the punishment, though, each leaf can reach a length of up to four metres (13’), giving a mature welwitschia a width of up to eight metres (26’) across.

Welwitschia’s answer to the pinecone.
(Image by Friedrich A. Lohmuller)

As you might expect from a long-lived relic of the past, there aren’t a lot of these plants around. For once, this has less to do with human disturbance than natural circumstances. Over millions of years, the range where welwitschia grows has dried out considerably, and in fact continues to get drier even now. Today, the plant relies largely on fog to meet its water needs, restricting its range to a thin strip of desert coastline where fogs occur regularly. Unlike cactuses or succulents, welwitschia has never evolved the ability to store water. Also problematic is a fungus, Aspergillus niger, which frequently infects and destroys germinating seeds. These factors together can mean that a welwitschia colony can sometimes go many years without successfully reproducing.

And of course, no threatened species would be complete without some human interference. In recent decades, unscrupulous collectors have removed plants from already small breeding populations, making it even more difficult to sustain their numbers. Interestingly, it’s noted in Wikipedia that plants in Angola are actually better protected from collecting than those in Namibia due to the higher concentration of landmines there.

So… landmines: bad for humans, good for endangered plants.

You think you have problems with split ends?
(Via: Natural History Museum)

Says Who?

  • The Gymnosperm Database
  • Dilcher et al. (2005) American Journal of Botany 92(8):1294-1310
  • Henschel & Seely (2000) Plant Ecology 150:7-26
  • Jacobson & Lester (2003) Journal of Heredity 94(3):212-217
  • Rodin (1958) American Journal of Botany 45(2):96-103

Killing Me Softly, or, The Fatal Embrace of the Strangler Fig

(Via: Wikimedia Commons)

Common Name: Strangler Figs

A.K.A.: Ficus species

Vital Stats:

  • There are around 800 sp. of figs, over half of which are hemi-epiphytes, like stranglers
  • Around 10% of all vascular plants are epiphytes (about 25,000 species)
  • The trees which produce the figs we eat are terrestrial, and do not grow in other trees

Found: Tropical forests of Latin America, Southeast Asia, and Australia

It Does What?!

What does it take to squeeze the life out of a full-grown tree? A lot of time and some very long roots, apparently. Many parasites eventually bring about the untimely death of their hosts, but few do it as slowly and as insidiously as the strangler fig.

Stranglers begin life as a tiny seed that leaves the back end of a bird and happens to land on a tree branch high in the rainforest canopy. The seed germinates, and the young fig begins to grow as an aerial plant, or epiphyte, taking its moisture from the air and its nutrients from the leaf litter on its branch. Thousands of plant species, including most orchids, grow in this manner. But then an odd thing begins to happen. The seedling produces a single long root. Very long. From tens of metres up in the canopy, this root grows all the way down to the ground. Many young stranglers will die before their questing root reaches the earth, but for those that make it, a connection is formed with the soil through which water and nutrients can be extracted. From this point on the great, towering giant which holds this tiny little interloper is in mortal danger.

The strangler fig, playing “harmless epiphyte.”
(Screenshot from The Private Life of Plants, BBC)

A secure connection to the soil allows the fig to speed up its growth and to begin sending more and more roots earthward. Rather than dropping straight down, like the initial root, these later organs will twine around the bark of the host tree. At first, the roots are tiny, like mere vines crawling over the host trunk. Over time, however, they thicken, covering more and more of the trunk’s surface. Where they touch or overlap, the roots actually fuse together, forming a mesh over the surface of the bark. Up above, the stem of the strangler is growing as well. It rises through and above the host branches, soaking up the light and leaving the other tree shaded and starved for energy.

In fact, this is a war fought on two fronts. As the starving host tree struggles to gather light energy to send downward from the leaves, it is also increasingly unable to bring water up from its roots. This is because the tree’s trunk continues to expand even as the strangler’s grip grows tighter around it. These opposing forces effectively girdle the tree, crushing the vascular tissues that carry moisture from the soil. Eventually, the battle is lost and the tree dies. Fortunately for the fig, its major investments in root growth have paid off – the dead host tree does not fall, taking the strangler with it. Instead, it simply rots where it stands. Finally, many years after its arrival on the scene, the strangler fig has achieved independence. It is now a free-standing tree, completely hollow and supported by its interwoven lattice of aerial roots.

The first root finds the ground.
(Screenshot from The Private Life of Plants, BBC)

So what happens when more than one strangler fig seed lands on a particular tree? Something quite unique… the roots of the different individuals fuse and form an organism which is indistinguishable from a single tree, except by molecular testing. These are what biologists refer to as ‘genetic mosaics.’ What’s more, the individuals actually begin to act like a single tree. You see, figs typically have staggered flowering times, such that it is unlikely for numerous trees in a small area to be in bloom at the same time. This helps in keeping their wasp symbionts well nourished. Once trees fuse, however, they seem to become physiologically linked as well, with researchers reporting that they bloom as a single individual.

The most hurricane-proof tree ever.
(Screenshot from The Private Life of Plants, BBC)

[Fun Fact: Some strangler fig species have very high growth rates, and huge individuals have actually been found engulfing abandoned buildings in the tropics.]

Says Who?

  • Harrison (2006) Journal of Tropical Ecology 22(4): 477-480
  • Perry & Merschel (1987) Smithsonian 17: 72-79
  • Schmidt & Tracey (2006) Functional Plant Biology 33: 465-475
  • Thomson et al. (1991) Science 254: 1214-1216
Don’t meditate under strangler figs.
(Via: Flickr, by vincenzooli)

The Bloodhounds of the Plant World (Cuscuta sp.)

(Via: Marine Science)

Common Names: Dodder, Goldthread, Witch’s Shoelaces

A.K.A.: Genus Cuscuta

Vital Stats:

  • Approximately 200 species
  • Part of the Convolvulaceae family, which includes morning glory and sweet potato
  • Only 15-20 species are considered to be problematic crop parasites

Found: Throughout temperate and tropical parts of the world

It Does What?!

We’ve discussed a few parasites on this blog already, and they’ve all been pretty typical of what comes to mind when we think of parasitic organisms- tiny, malignant little creatures that invade the host’s body, steal its resources, and, in some cases, eat its tongue. But when we think ‘parasite,’ we don’t usually think ‘plant.’ As it turns out, there are an estimated 4500 parasitic species just among the angiosperms, or flowering plants. Among them, dodders have to be one of the strangest.

Found nearly throughout the world, these vine-like plants begin as tiny seeds that germinate late in the spring or summer, after their potential host plants have established themselves. The young seedling has no functional roots and little or no ability to photosynthesize, so initially, it must make do with what little nutrition was stored in its seed. This isn’t much, so the plant has only a few days to a week to reach a host before it dies. To better its chances, the dodder stem swings around in a helicopter-like fashion as it grows, trying to hit something useful.

Much more impressive is the plant’s other method of finding suitable hosts- a sense of smell. Recent research has found that, uniquely among plants, the dodder can actually detect odours given off by surrounding plants and grow towards them. In experiments, the seedlings were found to grow toward the scent of a tomato, even if no actual plant was present. What’s more, they are capable of showing a preference among hosts. Presented with both tomato plants, which make excellent hosts, and wheat plants, which make poor hosts, seedlings were found to grow toward the aroma of tomatoes much more often. Like herbivores, they can use scent to forage amongst a variety of species for their preferred prey.

Smells like lunch… even to other plants.
(Via: Wikimedia Commons)

Once a host plant is found, the dodder begins to twine itself around the stem and to form haustoria (singular: haustorium). These are like tiny tap roots that pierce the host’s stem and actually push between the living cells inside until they reach the vascular system. Once there, the haustoria enter both the xylem (where water and minerals move upward from the roots) and the phloem (where sugars from photosynthesis move around the plant). From these two sources, the dodder receives all its nutrients and water, freeing it from any need for a root system, or even a connection to the soil. And since it doesn’t need to capture solar energy, all green pigment fades from the parasite, and it turns a distinctive yellow or red colour. Leaves aren’t necessary either, which is why the plant is essentially nothing but stem, explaining its common name of “witch’s shoelaces.”

Not what you want to see when you head out to weed the garden.
(Via: County of Los Angeles)

Once it gets comfortable on its new host, the dodder can grow at a rate of several centimetres a day (impressive for a plant) and produce stems of a kilometre or more in length, quickly overrunning an area. It can also attach itself to additional hosts – hundreds, in fact – which is problematic, because at this point it becomes the plant equivalent of a dirty shared needle. Since the vasculature of the hosts is connected, any virus present in one host can be freely transferred to any other. This ability, coupled with its affinity for potatoes, tomatoes, tobacco, and several other important crops, makes dodder a major nuisance for many farmers. And since it’s able to regenerate from just a single, tiny haustorium left in a host plant, it’s really hard to get rid of. There’s always a flip side, though; in some ecosystems, dodder can actually maintain biodiversity by preferentially parasitising the more competitive plants, allowing the weaker ones to survive. It seems dodder may also be the Robin Hood of the plant world.

[Extra Credit: Here’s a video showing how dodder can completely take over a group of nettle plants, complete with ominous soundtrack. Narrated by the fantastic Sir David Attenborough.]

Says Who?

  • Costea (2007-2012) Digital Atlas of Cuscuta (Convolvulaceae). Wilfred Laurier University Herbarium, Ontario, Canada
  • Furuhashi et al. (2011) Journal of Plant Interactions 6(4): 207-219
  • Hosford (1967) Botanical Review 33(4): 387-406
  • Pennisi (2006) Science 313: 1867
  • Runyon et al. (2006) Science 313:1964-1967

    Cuscuta: 1, Acacia: 0
    (Via: Wikimedia Commons)

Missing Carpels & the Building Blocks of Science

(Photo by: Domingos Cardoso)

Common Name: Amarelão (Brazil), Grapia (Argentina), Khare Khara (Bolivia)

A.K.A.: Apuleia leiocarpa

Vital Stats:

  • Once considered a genus of three different species, now collapsed down to one by taxonomists
  • The only trimerous (three-parted) flower in the whole legume family
  • Male flowers grow an extra stamen in place of the missing carpel

Found: In the rainforests of central South America

It Does What?!

Nothing quite as bizarre as our usual subjects, actually, but stick with me here. This week, I’m attending the annual conference of the American Society of Plant Taxonomists in Columbus, Ohio. I’ll be giving a talk on some of my research dealing with Apuleia and the development of its flowers. I thought I’d take this week to share some of that research here, and to try to make it interesting for people who aren’t into obsessing over obscure plants. If you still find this entry painfully tedious, though, rest assured, we’ll be back to freaks and oddities next week.

Apuleia leiocarpa is part of the legume family, which, if you’re from a temperate part of the world, brings to mind little annuals like beans and peas and clover. In the tropics, though, legumes are just as often towering trees of the rainforest canopy (like Apuleia) or scraggy shrubs of arid grasslands (such as Acacia). Most of the nearly 20,000 species of legumes have flowers with the same basic groundplan: 5 sepals, 5 petals, 10 stamens (the male organs), and a single carpel (where the fruit and seeds form). There are closely related chunks of the family, though, in which some of these floral organs have been lost over the course of evolution. (Now, ‘lost’ can mean two things; either the organ starts to grow and is suppressed before it finishes developing, or it just never forms at all. To the naked eye, these two kinds of loss look exactly the same. I’ll come back to this later.) Apuleia is one such legume- it has entirely lost two of its sepals, two of its petals, and most of its stamens, making for a very simplified flower.

The Hermaphodite (‘Normal’) Flower
S=sepal, P=petal, A=anther/stamen, C=carpel, St=stigma

What’s more, it now forms two different types of flower (called ‘morphs’). If you were to look closely at a flowering branch on one of these trees, you would see that the vast majority of the flowers were male-only, having no carpel with which to form fruit. Only every fourth or fifth flower would be the hermaphrodite type that we think of as a ‘normal’ flower. Botanists refer to this type of plant as being andromonoecious (pronounced “an-dro-mon-ee-shus”). So why would a tree evolve to become andromonoecious? There are a couple of different theories, based on two different ways that the male-only flowers can be produced.

In the first and most common type of andromonoecy, all the flowers on the plant begin as normal hermaphrodites. There are flowers of all different ages, so while some are beginning to open, others haven’t finished forming yet. Pollination starts on the earlier flowers, and the plant detects that it has far more ovaries (future seeds) than it’s going to need. Maybe the soil isn’t providing enough nutrition to produce all those potential fruits, or maybe there’s a drought in progress. So, according to its needs, the tree simply suppresses the development of the carpels in the younger flowers before they have time to mature, leaving parts of each branch with hermaphrodite flowers and parts with male flowers.

The Male-Only Flower
S=sepal, P=petal (both removed)
Arrow= where the carpel would have been

In scenario two, some flowers never develop carpels; they are male-only from the time they are first formed. This type of andromonoecy is thought to occur because the tree requires large amounts of pollen to reproduce successfully (perhaps the species is wind pollinated and individuals tend to be far apart, for example), and it’s “cheaper” to produce male flowers than hermaphrodites. In this situation, we don’t see the pattern of younger versus older flowers with respect to which ones are male.

That white asterisk in the very middle shows the hole through which the carpel would have emerged. It’s just a small, empty cavity in the male flower.

So which type of andromonoecy does Apuleia have? In order to find out, a colleague and I studied pressed herbarium specimens as well as flowers preserved in alcohol. The flowers, we dissected and viewed under an incredibly powerful microscope called a scanning electron microscope, which allowed us to see minute details, such as where a suppressed carpel might have been. In the end, we found that male Apuleia flowers show no sight of having ever developed a carpel. We also noticed that the hermaphrodite flowers always occurred symmetrically, right in the centre of a group of male flowers, a pattern that we wouldn’t see if the andromonoecy was environmentally influenced.

So in the end, we’re able to say that in this species, the different floral morphs probably arose in evolution due to an increased need for pollen, rather than as a control on fruit production. Groundbreaking… right? Well, maybe not, but obscure little discoveries like this are the building blocks for the big important breakthroughs we read about in the news. If you want to make something huge, you need a good foundation to start from.

Now imagine spending three hours of your life staring at this.
Science is so glamourous.

Says Who?

  • Beavon & Chapman (2011) Plant Systematics and Evolution 296: 217-224
  • de Sousa et al. (2010) Kew Bulletin 65: 225-232
  • Gibbs et al. (1999) Plant Biology 1: 665-669
  • Spalik (1991) Biological Journal of the Linnean Society 42: 325-336
  • Zimmerman et al. (In Press) International Journal of Plant Sciences

EVOLUTION TAG TEAM, Part 2: Sex & the Synconium

The second in an ongoing series of biology’s greatest duos. (Check out Parts One and Three)

(Via: Mastering Horticulture)

Common Name (Plants): Fig Trees

  • A.K.A.: Genus Ficus

Common Name (Wasps): Fig Wasps

  • A.K.A.: Family Agaonidae

Vital Stats:

  • Approximately 800 species of figs
  • Most are trees, but some are shrubs and vines
  • Approximately 640 species (20 genera) of fig wasps
  • All are obligate pollinators of figs

Found: Throughout the Tropics

It Does What?!

Snacked on any Fig Newtons lately? Tasty, right? Like the ad says, “A cookie is just a cookie, but a Newton is fruit and cake.”  …And wasps.

They must have run out of space on the package for that last part.

Before you toss out your favourite teatime treat, I should point out that without those wasps, the figs themselves wouldn’t exist. [Personally, I love Fig Newtons and will eat them regardless of any insects present.] This plant-insect pairing actually represents one of the most stable symbioses out there, with evidence suggesting it has existed for over 65 million years.

Now with 10% more Wings
(Via: Wikipedia)

While it’s not entirely clear how this arrangement evolved in the first place, fig trees produce a unique structure called a synconium, in which the flowers are actually inside the part we think of as the fruit. This synconium, which can contain up to 7000 flowers, depending on the fig species, has a tiny hole at the tip called an ostiole. In order for the flowers to be pollinated and the fruit to grow, a female wasp must squeeze through that hole, often losing her wings and antennae in the process, and distribute pollen that she carries in a sac on her abdomen. As she does so, she also uses her ovipositor to reach down into some of the female flowers and lay her eggs in their ovaries, where a gall is formed and the larvae can develop. Then she dies and ends up in a cookie. The End.

But hold on, let’s remove humans from the equation for a moment. She dies, but her eggs hatch into little moth larvae which use the growing fig for nutrition. Once they’re old enough, the young wasps mate with one another inside the fig (another nice mental image for snacktime), and the females gather pollen from the male flowers and store it inside their abdominal pollen baskets (yes, that’s actually what they’re called). The wingless male wasps have a simple, three step life: 1) mate with females, 2) chew a hole through the fig so they can leave, 3) die. That’s pretty much it for them. They may escape the nursery with the females, but they’ll die shortly thereafter, regardless. In fact, even the females have a pretty rough deal; from the time they’re old enough to mate, they have about forty-eight hours to get their eggs fertilized, gather pollen, find a new synconium, distribute the pollen, and lay their eggs. Two days, and their life is over. No pursuit of happiness for the fig wasp, I’m afraid.

“What does it all mean?”
(Via: BugGuide.net)

As with any long-standing mutualism, there are, of course, parasites ready and waiting to take advantage of it. These parasites are wasps which are able to enter the synconium and lay their eggs, but which do not pollinate the fig. Although their eggs will crowd out those of the fig wasps, decreasing the number of fig wasp larvae born, they are kept in check by the fact that any unpollinated synconium will be aborted by the tree and drop to the ground, taking the parasite eggs with it. The nonpollinating wasps are therefore kept from being a serious threat to the tree’s pollinators.

So there you have it, another of evolution’s great matches. The wasps get an edible nursery, the trees get pollinated, and we get tasty fruits with suspicious crunchy bits that probably aren’t dead wasp bodies, so just try not to think about it too much…

Seeds, or wasp eggs? You be the judge!
(Via: This Site)

[Fun Fact: The symbiosis between fig species and their corresponding wasp partners is so specific (often 1:1), that the shape of the ostiole actually matches the shape of the head of the wasp species which will pollinate it.]

[For those who would like to read about figs and fig wasps in much greater detail (such as how this works when the male and female flowers are in different figs), check out this excellent site for all you could ever want to know.]

Says Who?

  • Compton et al. (2010) Biology Letters 6: 838-842
  • Cook et al. (2004) Journal of Evolutionary Biology 17: 238-246
  • Kjellberg et al. (2001)Proceedings of the Royal Society of London, Biology 268: 1113-1121
  • Proffit et al. (2009) Entomologia Experimentalis et Applicata 131: 46-57
  • Zhang et al. (2009) Naturwissenschaften 96: 543-549