Showing posts with label last common ancestor. Show all posts
Showing posts with label last common ancestor. Show all posts

Wednesday, January 7, 2015

The Fungus And The Frog

Biology concepts – common descent, evolution, direct descent, fungi, undulipodia, amphibians, phylogenetics

THIS IS NOT HOW EVOLUTION OCCURS!! What this
animation implies is that one type of animal became
another type of animal. It shows a chimp becoming a
human. If so, how come there are still chimps? This
suggests direct descent with adaptation and this is a
fallacy. What is correct is that the animals shown did all
share a common ancestor at some point.

The first life on Earth is a mystery to us. Our best guess right now states that whatever it was, it showed up about 3.5-3.7 billion years ago. It was a cell, let’s call him Luca (last universal common ancestor). Luca had DNA, or maybe just RNA. He had ways to harness and use energy for his purposes, to adapt to changes in his environment, and to reproduce. Luca possessed all seven of the characteristics of life.  

Every living thing you see around you, and all the living things you can’t see around you, are descended from Luca. But here is the part that’s a little harder to understand – it hasn’t been a straight line from Luca through all other life forms to you.

It’s the difference between common descent and direct descent. Just because humans and pine trees have a common ancestor, it doesn’t mean that we are direct descendents of the same organism.

At some point, about 3.5 billion years ago, archaeal prokaryotes were recognizable. Luca gave rise to archaea and also to bacteria, but we can’t say that bacteria descended directly from archaea. There are as many differences between archaea and bacteria as there are between you and a pine tree, maybe more. All we can say is that they diverged from a common ancestor, which is why they have some common characteristics (from a common ancestor), and many different characteristics (because they diverged).


This is a much better representation of evolution
through common descent and adaptation. We may not
know what exact organism was the last common ancestor
between any two branches since only the fossil record only
represents about 1% of species that lived.
Bacteria were, and are, just about perfect organisms. They were bacteria then, and they are bacteria now - why mess with perfection. They have diverged into many types of bacteria, and those types are diverging even today, but they have stayed as bacteria.

Archaea, as opposed to bacteria, diverged again and again, giving rise to the rest of the kingdoms we know today – protists, plants, fungi, and animals. The question is, why did they diverge so much, while bacteria stayed so much the same?

I don’t know the answer, but a good theory is the development of organelles. We have talked before about how an archaea swallowed a bacteria, but didn’t destroy it, and how that the eukaroytic nucleus. Another instance in this endosymbiosis theory formed the mitochondrion. The more complex something is, the more chance for it to respond to changes in the environment – more adaptation could have led to more divergence.

Through billions of years of struggle and adaptation, the eukaryotic kingdoms emerged – but again, you can’t say that one descended directly from another. Contrast evolution to the alphabet. C follows B, which follows A. Humans like to think linearly. But consider that there may be millions of A’s. Must they all become B’s and then C’s?

No, millions of A’s may breed and remain A’s over the years, while what became a B breeds and stays a B. Maybe later on a couple of A’s breed and have a little baby that looks like neither an A nor a B. Now we have C. B and C or both diverged from A, but B and C are different from one another. They are linked by common, but not direct, descent.


This is a phylogenetic map of the life on Earth. Notice that
we don’t know just what the last common ancestor was, but
you see that eukaryotes diverged from archaea and that
animals, plants, and fungi diverged from protists
(microsporidia, flagellates, ciliates, slime molds) rather
recently. Trees may look a bit different based on what DNA
target gene is being compared.
Scientists use changes in DNA over time to track just when two lines of organisms diverged from their last common ancestor. They can plot this out by time and distance, forming a diagram. This is the study of phylogeny (from Greek phylos = race, and genesis = birth of) and its tools are phylogenetics. Because the diagrams can look like trees, with the common ancestor as the base of the trunk, they are called phylogenetic trees.

A long time ago, a few archaeal descendents had diverged enough to be called protists. They were eukaryotic now, with organelles and special functions, and were starting to think about working together as multicellular organisms. The protists of that time were direct descendents of archaea, but the different protists we know today (see our last few posts here, here, and here) aren’t necessarily directly descended from one another or even from the same archaea.

Some protists diverged from one another. Many stayed as protists, even though they might have evolved to different orders or families over the years. However, others became animals, fungi, or the plants. Our last common ancestor with plants was a protist of some sort, so we have a common ancestor with a pine tree, we just can’t draw a direct line through humans and a pine tree to get to that ancestor.

Let’s use undulipodia (eukaryotic flagella and cilia) to illustrate, or confuse, the situation. We saw that protists – most all of the different protists, use flagella or cilia in one or several ways. Flagella and cilia are characteristics that have been retained in the various descendents of archaea…. But didn’t we also say that prokaryotic flagella and eukaryotic undulopdia are completely different in structure and genes? Yes we did - so what gives.


This is a typical fungus that someone might think of. This is the
basidiomycete mushroom, Phallus indusiatus. Fungi can range
from single cell yeasts (yeah beer!) to hyphal forms that make
your tongue fuzzy, to mushrooms that can take up thousands of
acres. By the way, in New Guinea they worship P. indusiatus as
sacred and that lacy web is called an indusium.
The archaea that diverged to become eukaryotes lost their flagella at some point, and then very quickly evolved them right back again. The structure of the new flagella were different; made from different proteins and having a different structure, but they did about the same job(s).  This re-evolving of a flagellum (and cilium) must have occurred pretty quickly, because all the kingdoms that descended from those early eukaryotes (protists, plants, fungi, animals) have them to some degree or another.

Yet, if you look for undulipodia in the fungal species on Earth today, you’ll find them in only one of the five phyla. Again, what gives? Didn’t we just say that fungi descended from undulipodia containing ancestors?

Four of the phylums of fungus are grouped by characteristics, both genetic and life cycle – the Chytridiomycetes, the Zygomycetes, the Ascomycetes and the Basidiomycetes. The fifth phylum is called the imperfect fungi because we haven’t found a life cycle in them that we can place into one of the other four phyla. But when we do, as we have for some individuals imperfect fungi, they usually fall into the ascomycete or basidiomycete phylum.

However, only chytrid fungi have flagella. Every species in every other phylum of fungi has lost their undulipodia. If you are thinking in terms of phylogenetics – what does this suggest to you?

Yes, very good – the chytrids are probably the common ancestor for all the other fungi. Those that didn’t diverge enough and stayed chytrids retained their undulipodia, but at some point, others lost their flagella and kept on changing into all the other phyla of fungi over time.


Here is a phylogenetic tree of the fungi, showing that flagella
were lost after the other phyla diverged from the
Chytridiomycetes. On the bottom right is a microscopic image
of the mature sporangium of a chytrid fungus. The
zoospores are inside the sporangium. The dark filaments are
rhizobia, not flagella.
You could do the genetics studies to find out which phylum diverged first, and then which one diverged from that and so on, but it would be a waste of time – it’s already been done. The picture to the right shows the phylogenetic tree for four of the phyla of fungi (minus the bothersome imperfect fungi).

What is so different about the chytrids that they kept their flagella, while the others were suited to live without them? There must be something about the chytrids life cycle and/or environment that required the retention of their eukaryotic flagella. Well, they all live in water, maybe they need flagella to swim around. But look at the picture of the chytrid on the right, I don’t see a flagellum anywhere there.

The chytridiomycete name comes from the Greek chytridion, which means little pot.  The pot holds all their zoospores, their reproductive form. It is the zoospores that have the flagella, so they can swim away and establish themselves somewhere with less competition. But that isn’t a good enough explanation. Many water borne fungi come from the basidiomycete or ascomycete phyla, and they don’t have flagella in any of their life cycle stages. Hmmm.

We have tens of thousands of extant (living today) fungal species, and only about 750 or so have any undulipodia. This makes the chytrids exceptional, and is directly related to their being the common ancestor for all the other fungi. If undulipodia are so important that animals, protists, some fungi, and even some plants have them, then why is it that so many fungi seem to get along fine without them? Maybe they’re the exception.

Let’s tell one story of how the chytrid flagella are important. A species of chytrid, called Batrachochytrium dendrobatidis, is responsible for perhaps the largest vertebrate mass extinction in the history of the Earth - and it's going on right now. Most chytrids are sabrophyitc, meaning they eat dead tissue, but a few are parasitic, mostly on plants.


Although the chytrid infection is a large reason for amphibian
collapse, there are others. Mutagens in pollution are responsible
frogs with extra or missing limbs. You can imagine how that
might interfere with long life and mating. It turns out that
amphibians, being in and out of water, are especially vulnerable
to environmental changes.
B. dendrobatidis, on the other hand, is the only known chytrid parasite of living animals - amphibians specifically. The fungi embed themselves in the keratinized skin of amphibians that find themselves in chytrid-contaminated water and then proceed to digest their skin. As many as 6000 species may be vulnerable to this fungus, and several hundred have gone extinct because of it.

You may have heard of the frightening loss of amphibian diversity on the past decades. The reasons for this are known to be several, including toxic pollutants, climate change, and habitat destruction. But B. dendrobatidis has played a significant role as well. Fortunately, a 2011 study showed that a water flea has a voracious appetite for our frog foe and might be used as a control measure. Unfortunately, a 2013 study showed that chytrid-susceptible amphibians may be succumbing to at least two different, and probably more, species of Batrachohytria. So the problem is probably more complex than we thought.

And yes, you read correctly a couple of paragraphs above. Some plants have cells that have flagella. There are moving plants cells! Those will be our exceptions for next week.




Martel, A., Spitzen-van der Sluijs, A., Blooi, M., Bert, W., Ducatelle, R., Fisher, M., Woeltjes, A., Bosman, W., Chiers, K., Bossuyt, F., & Pasmans, F. (2013). Batrachochytrium salamandrivorans sp. nov. causes lethal chytridiomycosis in amphibians Proceedings of the National Academy of Sciences, 110 (38), 15325-15329 DOI: 10.1073/pnas.1307356110

Buck, J., Truong, L., & Blaustein, A. (2011). Predation by zooplankton on Batrachochytrium dendrobatidis: biological control of the deadly amphibian chytrid fungus? Biodiversity and Conservation, 20 (14), 3549-3553 DOI: 10.1007/s10531-011-0147-4




For more information or classroom activities, see:

Common descent –

Fungi –

Amphibian collapse –

Phylogenetics –



Wednesday, June 19, 2013

The Roots Of Our Animal Family Tree

Biology concepts – porifera, last common ancestor, placozoa, cladogram, lower metazoan, bilaterians

Bonobo apes (Pan paniscus) are very closely related to
chimpanzees. They have longer legs than common
chimpanzees (Pan troglodytes) and are also
distinguished by having pink lips. I think this makes
them look significantly more human-like. Also like
humans, the families seem to be run by the mothers.
Humans are descended from primates; we share 99% of our DNA with chimpanzees and Bonobos (pygmy chimps). But what do we find as we go farther back along the line of mammals, and then from animals in general?

Question of the Day:  What ancestor gave rise to all the animals and is it still around today?

This is a much tougher question than it would seem at first glance. When I was studying biology for the first time, I thought that since humans descended from apes, and we see apes, then apes must have diverged from some other animal type that we recognize – something like apes descended from rodents.

But evolution doesn’t have to work this way; not every group of animals has evolved directly from some other group of animals. At some point, mammals had a last common ancestor with some other group of animals, and before that, those ancestors had a last common ancestor with some older group, and so on until the last common ancestor was the organism that gave rise to the first animal.

So did me need a mammal to give rise to all mammals? It is much like - which came first, the chicken or the egg? We all know that dinosaurs were laying eggs millions of years before chickens, but try thinking of it like this – which came first, the chicken or the chicken egg?

In terms of evolution, there was some bird like animal that was almost what we would agree was a chicken genetically; let’s say it was missing just one mutation or rearrangement of genes that prevented it from being called a chicken. So this non-chicken lays an egg. The embryo inside just so happens to contain the very mutation or change that will let us call it a chicken. Is it a chicken – yes.  In a chicken egg – no. The chicken came first.

The chicken or the egg question is much more interesting
than most people realize. Consider what you call a chicken
egg – is it an egg from a chicken, or an egg that houses a
chicken? If you think it is an egg that develops around an
embryonic chicken, then the egg came first, as opposed to
the explanation in the text. I love discussion about what
words mean, they make us thinkers.
Our discussion of the non-chicken egg description makes it easier to imagine that there was some organism that, while not an animal, was mother to all animals. The question still remains as to how that animal might have looked or behaved – but that won’t keep us from looking at some possibilities.

It would be a nice feather in your cap if you were the person to discover evidence of the first animal. In 2012 there was one article that displayed fossils of track marks from possibly 585 million years ago – pushing back the previously accepted date of animals by 30 million years.

Yet there was another 2012 paper showing Namibian fossils that could be 760 million years old – pushing the start date of animals back more than 200 million years! The truth may be somewhere in between, or might be even earlier. However, fossils of the first animals, if they exist, would only give limited information. Can we look further?

The 760 million year date is in line with what some geneticists estimate for the first animal. By looking at genes that all animals have in common and the rates at which those genes change over time, scientists can backtrack to see when they might have emerged.

What if we look at today’s animals, and which may best represent the first animal. Are we talking about primitive animals? What does it mean to be a primitive animal? If an animal species was closely related to the last common ancestor of all animals, it would be easy to say that it was a primitive animal – it lived long ago when animals were new, and it had a lot in common with the first, most primitive animal.

But do not confuse a species or genus with an individual animal. We have animals today whose ancestors were very closely related to the first animal, but that doesn’t mean that these individuals are primitive – they could have undergone extensive evolution through the millennia. Quite a number of adaptations could have taken place that increase the complexity of the animals biochemistry and/or behaviors.

The last common ancestor is sometimes called the most recent common 
ancestor (MRCA). They both mean the same thing. This chart 
pinpoints the MRCA for all life on Earth. That does not mean that it 
gave rise to all life. There could have been several parallel lines that all died
off. Same for the animals – there could be whole animal
phylums we know nothing about.
On the other hand, we can look at organs and systems as a measure of complexity or primitiveness. All animals are classified as metazoans (meta = changing, zoa =  animal). Some are termed lower metazoans, because they do not have complex structures like spinal chords (chordates) or bilateral symmetry (bilaterians).

Organization makes animals more complex as well. Cells of different types can form tissues that have specific functions. Tissues can organize into organs and organs join together to form systems. Animals without these characteristics are termed “lower” or “simple” or “primitive.”

Likewise, animals that can’t perform behaviors that other animals can are supposedly more primitive. If one species can move while another can’t, then the sessile (non-moving) animal is more primitive. Nervous systems are supposedly a big feature of more complex animals.

These ideas can lead to great discussions relating cells to life. What does it mean for one culture to be more primitive than another. Does a lack of cell phones make you primitive? Amazonian cultures had been using certain medicines for thousands of years before we arrived and stole their pharmacology. Now who looks primitive?

All this being said, can we learn anything by looking at extant (living) species as representatives of what early animals might have looked like or how they might have behaved? Yes, I think we can. You can’t know where you are going if you don’t know where you’ve been.

Sponges might be a good place to start. Sponges are so primitive that most non-scientists don’t even think of them as animals. Most have no body symmetry, they appear to be sessile, and they have a very few cell types, none of which are organized into tissues or organs or systems.

Sponges have been around for about 760 million years, if we are to accept the Nambian fossils as well-dated and representative of the earliest sponges. This would put them in the front seat of the animal bus. But are they really that primitive?

This is the harp sponge (Chondrocladia lyra) that was discovered off 
the coast of Oregon, Washington state and Canada. It lives in the 
trenches below 3000 m and represents just one of the carnivorous
sponges. You want weirder, loo up a picture of the ping pong tree sponge!
Sponges generally have three different regions, the outer layer, the more acellular mesohyl, and the inner surface. Choanocytes line the inner surface and have a single flagellum that help the cell to harvest floating food in the filtered water. The outer layer is made up of pinacocytes that filter the water and digest food particles too large to be filtered. So far, interesting but not amazing.

But the mesohyl of this “primitive” animal has some cool stuff.  There are motile cells that secrete collagen protein. There are muscle cells that help the sponge contract and relax. There are “grey” cells that act as an immune system. And there are other motile cells that are totipotent stem cells and can become any cell type with in the sponge. Still sound primitive?

If you want a nice example of just how complex sponges can be, meet the harp sponge (Chondrocladia lyra). It is definitely a member of the phylum porifera (Latin for “bearing pores”), but it does have elegant symmetry. Described in late 2012, the harp sponge is also one of about 24 different carnivorous sponges.

The harp sponge uses sharp spikes on the vertical growths to harpoon and hold fish and crustaceans, which it then wraps them on a membrane and digests whole. This is in contrast to most sponges that filter microscopic food particles from the water by passing the water through its body from the outside and then up and out of its chimney (see video).

Trichoplax adharens may represent the most basal animal alive. Made
up of just a few thousands cells of only four different types, it has the
smallest genome of any known animal. The cutaway drawing on the
right shows that there are layers of cells, so it does have some
organization, just no tissues or nervous system.
The harp sponge is like other sponges in that it can reproduce asexually through fractured off pieces, by gemmules that are like clonal spores, or by budding. They can also reproduce sexually, but in the harp sponge the spermatophores are not simply released form the sponge body. They gather in the bulb portion at the top of the vertical shafts and are released all at once. The oocytes are found in the middle bulges. Sponges can reproduce four different ways while we only have one. We can, and will, spend more time on the exceptions that are sponges.

In recent years, less emphasis has been placed on sponges as a basal form of animal and more attention has been given to the placozoans (placo = flat, and zoa = animal). Only one species of placozoan is known (Trichoplax adharens) has been described, mostly because they have never been observed in their natural habitat (ocean, we think) and have only been seen on the walls of laboratory and zoological aquariums.

Placozoans have only four different cell types, no symmetry, two layers of cells, and no nervous system. Even by sponge standards, this is awfully primitive. The 2009 study of Schierwater et al. has given the best proof that T. adharens is the most basal of the lower metazoans, based on comparisons of thousands of genetic loci.  This agreed with several earlier studies, but Dr. Schierwater’s group went much further.

The cladogram on the left dates from 2009, showing that a more primitive
animal gave rise to both the lower metazonas and separately to the more
complex animals. The tree on the right is from 2013 symposium write up
in Integrative and Comparative Biology (doi:10.1093/icb/ict008), and
represents a consensus of the genetics data and opinions. They seem to
think that sponges diverged early than all the rest of the animals. Needless
to say, opinions vary.
Their cladogram evidence seems to indicate that sponges, cnidaria, ctentophora (comb jellies), and placozoans diverged as a single group and in parallel with bilaterian animals. Together, these data mean that as a group, the lower metazoans diverged from the more complex metazoans even before the emergence of sponges or placazoans (see cladogram). Complex animals did not evolve from sponges, jellies or placozoans at all – they came from some different ancestor.

So, this evidence suggests that there was something out there that was an ancestor of both the lower metazoans and the bilaterians, but was itself neither of them – an animal whose ancestor wasn’t an animal. Will we recognize it when we see it? It leads to another question. What will it have to have to be considered the first animal and not the last non-animal – just what makes an animal an animal?

Next week - how do stars determine the color of plants, and what colors might alien plants be?



Dohrmann, M., & Worheide, G. (2013). Novel Scenarios of Early Animal Evolution--Is It Time to Rewrite Textbooks? Integrative and Comparative Biology DOI: 10.1093/icb/ict008

Schierwater, B., Eitel, M., Jakob, W., Osigus, H., Hadrys, H., Dellaporta, S., Kolokotronis, S., & DeSalle, R. (2009). Concatenated Analysis Sheds Light on Early Metazoan Evolution and Fuels a Modern “Urmetazoon” Hypothesis PLoS Biology, 7 (1) DOI: 10.1371/journal.pbio.1000020