Dissecting embryos from half a billion years ago

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There is a treasure trove in China: the well-preserved phosphatized embryos of the Doushantuo formation, a sampling of the developmental events in ancient metazoans between 551 and 635 million years ago. These are splendid specimens that give us a peek at some awesomely fragile organisms, and modern technology helps by giving us new tools, like x-ray computed tomography (CT), scanning electron microscopy (SEM), thin-section petrography, synchrotron X-ray tomographic microscopy (SRXTM), and computer-aided visualization, that allow us to dig into the fine detail inside these delicate specimens and display and manipulate the data. A new paper in Science describes a survey of a large collection of these embryos, probed with these new techniques, and rendered for our viewing pleasure…that is, we’ve got pretty pictures!

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Gogonasus andrewsae

Here’s another tetrapodomorph fish to consternate the creationists. These Devonian/Carboniferous animals just keep popping up to fill in the gaps in the evolutionary history of the tetrapod transition to the land—the last one was Tiktaalik.

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Skull in lateral view.

This lovely beastie is more fish than frog, as you can tell—it was a marine fish, 384-380 million years old, from Australia, and it was beautifully preserved. Gogonasus is not a new species, but the extraction and analysis of a new specimen has caused its position in the evolutionary tree to be reevaluated.

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Feminism is undermining human evolution!

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Human X (left) and Y (right) chromosomes

Did the internet get stupider while I was away this past week? I mean, it’s gratifying to my ego to imagine the average IQ of the virtual collective plummeting when I take some time off, but I really can’t believe I personally have this much influence. Maybe the kooks crept out in my absence, or maybe it was just the accumulation of a week’s worth of insanity that I saw in one painful blort when I was catching up.

What triggers such cynicism is the combination of Deepak Chopra, Oliver Curry, and now,
William Tucker. Tucker wrote a remarkably silly piece in the American Spectator in which he drew deeply faulty conclusions from human genetics to support a thesis rife with misogyny and foolish chauvinism on human evolution. It was like a piece on evolutionary psychology written by someone who didn’t know any genetics at all.

Hang on to your hats—we’re going to see a factoid from one magazine article balloon up into a declaration of the superiority of the male species (I use “species” here both ironically and mockingly).

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Evo-devo is not the whole of biology

Sometimes a plan just comes together beautifully. I’m flying off to London tomorrow, and on the day I get back to Morris, I’m supposed to lead a class discussion on the final chapters of this book we’ve been reading, Endless Forms Most Beautiful. I will at that point have a skull full of jet-lagged, exhausted mush, and I just know it’s going to be a painful struggle. Now into my lap falls a wonderful gift.

There was a review in the NY Review of Books that said wonderful things about Carroll’s work, and in particular about the revolutionary nature of evo-devo. This prompted Jason Hodin, an evo-devo researcher himself (whose work I’ve mentioned before) to write a rebuttal and send it off to NYRB…which they chose not to publish. So he sent it to me, with permission to post it.

(If Pharyngula is going to be second choice to the NY Review of Books, I’m not going to complain.)

Anyway, I’m almost as guilty as Carroll of hawking the wares of the evo-devo bandwagon and traveling roadshow, so this is a welcome balancing corrective. The complete text is below the fold.

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Evolution of sensory signaling

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How we sense the world has, ultimately, a cellular and molecular basis. We have these big brains that do amazingly sophisticated processing to interpret the flood of sensory information pouring in through our eyes, our skin, our ears, our noses…but when it gets right down to it, the proximate cause is the arrival of some chemical or mechanical or energetic stimulus at a cell, which then transforms the impact of the external world into ionic and electrical and chemical changes. This is a process called sensory signaling, or sensory signal transduction.

While we have multiple sensory modalities, with thousands of different specificities, many of them have a common core. We detect both light and odor (and our cells also sense neurotransmitters) with similar proteins: they use a family of G-protein-linked receptors. What that means is that the sensory stimulus is received by a receptor molecule specific for that stimulus, which then actives a G-protein on the intracellular side of the cell membrane, which in turn activates an effector enzyme that modifies the concentration of second messenger molecules in the cell. Receptors vary—you have a different receptor for each molecule you can smell. The effector enzymes vary—it can be adenylate cyclase, which changes the levels of cyclic AMP, or it can be phospholipase C, which generates other signalling molecules, DAG and IP3. The G-protein that links receptor and effector is the common element that unites a whole battery of senses. The evolutionary roots of our ability to see light and taste sugar are all tied together.

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Cool data!

Nick Matzke has
compiled all the data on hominin cranial capacities into a single chart:

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I think I can see a pattern there, can you? He also has data on body size and brain size over there, take a gander at it. It looks like a simple and obvious example of evolutionary change in our lineage, I think.

Alas, it only shows specimens older than 10,000 years. I’m sure that right around 6,000 years ago, there was a sudden, dramatic change as the deity injected a soul into those crania.

Hox complexity

Here’s a prediction for you: the image below is going to appear in a lot of textbooks in the near future.

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(click for larger image)
Confocal image of septuple in situ hybridization exhibiting the spatial expression of Hox gene transcripts in a developing Drosophila embryo. Stage 11 germband extended embryo (anterior to the left) is stained for labial (lab), Deformed (Dfd), Sex combs reduced (Scr), Antennapedia (Antp), Ultrabithorax (Ubx), abdominal-A (abd-A), Abdominal-B (Abd-B). Their orthologous relationships to vertebrate Hox homology groups are indicated below each gene.

That’s a technical tour-de-force: it’s a confocal image of a Drosophila embryo, stained with 7 fluorescent probes against different Hox genes. You can clearly see how they are laid out in order from the head end (at the left) to the tail end (which extends to the right, and then jackknifes over the top). Canonically, that order of expression along the body axis corresponds to the order of the genes in a cluster on the DNA, a property called colinearity. I’ve recently described work that shows that, in some organisms, colinearity breaks down. That colinearity seems to be a consequence of a primitive pattern of regulation that coupled the timing of development to the spatial arrangements of the tissues, and many organisms have evolved more sophisticated control of these patterning genes, making the old regulators obsolete…and allowing the clusters to break up without extreme consequences to the animal. A new review in Science by Lemons and McGinnis that surveys Hox gene clusters in different lineages shows that the control of the Hox genes is much, much more complicated than previously thought.

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How would ID have contributed?

Carl Zimmer brings up another essential point about the HAR1F study: it was work that was guided by evolutionary theory. The sequence would not have been recognized in the billions of nucleotides in the genome if it hadn’t been for an analysis directed by the principles of evolution.

Wells’ diatribe was amazingly wrong. I looked at it again and there could be another half-dozen essays in just picking up apart the stupidity in it.