The Evo Devo conversation resumes!

I had a productive discussion with Phrenotopian, Jackson Wheat, and Nesslig 20 yesterday, in which I got lots of suggestions for how to make the science content of my YouTube channel more interesting. Now I just have to implement them! Starting on Wednesday!

I’m going to talk about evo-devo again, but with a revised format that allows for more actual discussion. So, on Wednesday at noon Central time, I’m going to fire up Zoom and Keynote and YouTube, all at the same time, and talk about Evolution of Coloration Patterns, a 2008 paper by Meredith Protas and Nipam Patel. You can give me feedback as we go in the chat, but also, if anyone wants to participate directly and put their face/avatar on screen, we can do that, too. Just send me an email, and I might send you a link back if 1) you promise to have read the paper, and 2) you think you have something to say.

I have other changes in mind for the future; maybe I’ll allow voice chat from the FtB Discord at some time. Not yet, though, but I’ll be experimenting.

Big boy gettin’ swole

Today was a big spider maintenance day. I’ve got three lines of spiders I’m raising — R (from a spider collected at Runestone park), H (from the local Horticulture garden), and M (from the Myers garage) which I’m trying to bring to maturity, so they’re getting lots of food and care, which I want to start inbreeding and generate 3 lines of related spiders so I can start assessing their variation…and then start cross-breeding. It’s going to take a while.

Anyway, down below the fold is one that’s definitely male and might be ready for mating after the next molt. His palps look painfully swole.

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Lunchtime in the lab

Not for me, of course — people don’t eat food in the lab — but for the adorable baby spiders, who got some delicious live flies and immediately wrapped them up and sucked their brains out. I’ve got two photos of two different spiders that adopted remarkably similar feeding behaviors, biting their prey in the head and slurping up their juices.

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A mundane cleaning day

Did you know classes start in 2½ weeks? It’s astounding; Time is fleeting; Madness takes its toll…but rather than doing the time warp, unfortunately, I spent several hours doing basic custodial work in the lab. First, a colleague and I scrubbed up the cell biology lab, shuffling computers into storage and putting away glassware, because that space will be used for a different course Spring semester. It’s tidy! And shiny!

Then I went into my lab, which is cluttered and grimy, and I need to make a few trips to a dumpster and polish up a whole lot of stuff — the sink is piled high with empty spider vials that need washing, for one thing. Today I set aside all the menial labor, though, and instead dismantled my microscope and cleaned up all the optics. That was fun! I may do it again tomorrow!

The filth wasn’t as bad as I feared, fortunately. One glass surface had accumulated a bit of dust and grime, and was fairly easy to wipe clean. I did have to take apart a few subassemblies, but thankfully, good German engineering made it easy.

I had to test it out with a few photos, but whereas the engineering was cooperative, the spiders were not. The entire interior of their condo cube was an intricate network of spider webs everywhere, so opening up the cube always tore their webs, making the kids frantic and excited, so they were mostly unwilling to sit still for their portrait.

I put a sample spider photo below the fold, and you’ll see what I mean — it’s all criss-crossed with silk, and I played a few lighting games to make it visible. Also note that the image is much, much better than the last spider photo I posted here.

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I haven’t cleaned the trinoc since when?

This morning I resolved to figure out what was going on with my muddy images from microscope. The first step was a general cleaning, and I discovered a real horror. Here’s the trinoc head for my Wild M3C:

See that tube on the right, for the camera? I looked down it. GAAAAAA. Dust and dirt and I swear, cobwebs all over. It’s a 30 year old microscope, and we’ve had microscope technicians come through every couple of years to do general maintenance on all the teaching scopes, but that tube may not have been cleaned ever in all that time. There’s a very important mirror down at the bottom of that L-shaped widget, and I think the only way I can get at it properly is to dismantle the whole device — there are a couple of tiny metric hex bolts holding it all together, and I guess I’m going to have to take it apart and try not to break everything.

Anyway, I did push the dirt around a little with a microfiber cloth, and it’s slightly better, but I think it’s filmed over with something that is fouling the image. I took a test photo of this little guy, and it’s an improvement, but still far from perfect. The image through the eyepieces is beautifully crisp, so I’m definitely blaming the problem on that little mirror and decades of neglect.

‘Ware spider below the fold!

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School portrait day

The spiders had to line up for their pictures today. I had a fixed routine, like a real portrait photographer.

  1. Fetch a spider condo cube from the incubator.
  2. Take a low power photo of the label, so I have a record of who is who on the camera ‘roll’.
  3. Carefully remove the lid to avoid startling the spider. They’ve already built elaborate cobwebs criss-crossing the chamber, so that didn’t always work. I wanted them still so I could get a focus series.
  4. Shoot a bunch of pictures.
  5. Spritz them with an atomizer of distilled water to gently convince them to change position. It also waters them — what was neat was watching them drink. A drop of water was roughly softball sized relative to the spider — they’d gather a droplet, bring it to their mandibles, and then you could see the droplet rapidly shrink as they slurped it down.
  6. Take another set of pictures.
  7. Flick a fly or two into the container as a reward.
  8. Put the condo back in the incubator.

It was a fun process, but I’m a little unhappy with the quality of the images — they’re not coming out very crisp. It may require some tweaking to compensate for the microscope adapter. Everything looks great through the eyepieces, but kind of squidgy in the camera output of the trinoc.

I’ll put one example below the fold.

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Salamander stories

The subject today is variation in limb development in salamanders.


Today I’m going to talk about salamanders and comparative anatomy. Comparative anatomy has been the gateway to evolutionary thinking for about two centuries — once you start counting up the similarities in different groups of animals and how the underlying pattern is reused over and over within a phylum, it’s inevitable that you start wondering what the source of the template might be (big hint: in the 19th century, it was proposed that the basis of the similarities was common descent, and that just keeps getting confirmed.)

In addition, salamanders, and amphibians in general, have been a major focus of embryology as well. They have the virtue of having numerous large eggs, often with recognisable spatial markings, and are amenable to all kinds of surgical manipulations. The first time I did embryo surgeries on a frog embryo, it was a revelation — it was like slicing into a sponge cake, while cutting into a zebrafish embryo was like operating on a soap bubble. It’s no wonder that amphibian work inspired Roux’s Entwicklungsmechanik, or developmental mechanics, over a hundred years ago, or that Mangold and Spemann’s classic work on the organiser was in a salamander. Developmental biology in the middle of the last century was tightly focused on amphibian work, until new tools in genetic manipulation opened up other organisms for experimentation.

Some of my happiest days as an undergraduate were spent in comparative anatomy labs, dissecting salamanders and cats and sharks and every dead thing I could get my hands on — I wasn’t above scooping up road kill. Tracing the intricacies of the skeletal and muscular system, finding homologies to little obscure muscles between a cat and a salamander, seeing how they varied…it was heavenly. I still have my vertebrate dissection texts, which had been periodically soaked in the fluids of the beasts, fresh or fixed, that I took apart in those days. I can pull them down off the shelf, open them, and still get a faint whiff of those fluids, and be instantly transported back to a dark basement lab and stainless steel benches, armed with dental picks and scalpels and fine forceps. Oh, the good old days.

By the way, the reason I have so many books is that I can’t bear to be parted from them. I never sold back my used textbooks — well, this one was probably unsellable — but kept them until they wore out.

Then in graduate school, a yearly event every fall was going up into the Oregon Cascades and collecting rough-skinned newts with the gentleman scholar Jim Kezer. We’d use them in a histology course, because they were an easy source of fresh tissue…and again we’d see all the wonderful similarities and interesting differences between amphibians and people at a different level of organisation. It’s not just genes that are related, but also tissues and organs and overall anatomy.

So let’s dive into an evo-devo paper from 1995 that doesn’t discuss genes at all, but just looks at the bones. It’s titled “Morphological Variation in the Limbs of Taricha granulosa: Evolutionary and Phylogenetic Implications”. I really like this paper for several reasons.

One: Taricha granulosa is the rough-skinned newt, the object of my excursions into the lovely Oregon mountains.

Two: It’s by Neil Shubin, David Wake, and Andrew Crawford. This is before Shubin became a famous celebrity scientist with the discovery of Tiktaalik, and one of the things it shows is that Shubin really put the work in. This is not a glamorous paper. When you read it, though, you learn exactly how important the background work is in science — he was prepared for Tiktaalik because he had a deep knowledge of anatomy and amphibian relationships.

Three: What first made me excited about this work was that it was a step away from the idealisation of our research animals. That is, we tend to develop a canonical image of how an organism is built, whether it’s a newt or a fish or a spider. When I was studying comparative anatomy, what we were comparing was THE cat to THE salamander to THE shark. This paper is comparing the anatomy of individuals within a single population to measure the extent of variation.

Four: Another factor in science in general is serendipity. Sometimes you get lucky, and you have to be prepared to jump on an opportunity.

The backstory of this study is that there was an abrupt freeze in December in California that froze a small pond solid, killing every large animal caught in it. In particular, an entire population of newts was killed overnight by a non-selective force, and when the pond thawed — I presume that happened shortly afterwards, it was in California, after all — the investigators could wade out and scoop up all the dead urodeles and throw them into fixative.

They collected over 500 animals, threw out the ones that were too decayed, and had 452 newts where they could examine the structure of the limbs (this paper focuses just on limb anatomy). This is cool: we can do comparative anatomy within a population, and ask questions about extant variation.

We’ll start with the standard anatomy of the limbs of Taricha. This is what you’d expect to see. It was also my least favourite part of vertebrate anatomy, all these tiny little odd-shaped wrist bones, like the scaphoid, the lunate, the capitate. I’m afraid I struggled with this stuff 45 years ago, and I’m sorry, it has completely evaporated from my brain since. I wonder if one reason I gravitated towards fish is that most of this complexity is gone in a teleost fin.

Fortunately, Shubin and his colleagues had a better awareness of the details than I ever did.

One approach you can take with this knowledge is to compare Taricha with other urodele species, and common theme in evolutionary biology, there are overall similarities, but also profound differences, often a consequence of some lineages having reduced and simplified their limbs. This would be the traditional approach.

But, as I said, Shubin and company are looking at variation within a single population of a single species. And that’s where it gets interesting. About 70% of the newts showed the canonical pattern — a clear majority! However, the 30% that are different are also important, since that variation is what evolution can work on. Those tiny wrist bones wobble in an interesting way.

We can also look at the details of specific variants. For instance, the hand of the animal has a specific pattern of 1 finger bone, then 2, then 3, then 2, or a 1-2-3-2 pattern.

Just looking at that attribute, 96.5% have the 1-2-3-2 pattern. But look, 1.5% lose the 3rd bone in the 3rd digit, and 0.5% add an extra bone to the second digit. This is awesome information, to get an idea of the actual variation in morphology in a population.

Then, further, to compare that variation to other species and determine that there might be deep rules that can shape the paths of least resistance for evolutionary variation. So Shubin writes in the discussion:

Bilateral patterns of variation in Taricha both restore ancient structures and “anticipate” derived conditions that arise in parallel within highly nested taxa. These regularities suggest that the same processes that underlie the expression of atavistic characters are involved in the origin of evolutionary novelties.

This little piece of the story reflects an ongoing interest in evo-devo: we often talk of “constraints” on development that limit the direction evolution can take, but the flip side of that is that these variations can also generate unexpected innovations in combination. I think of it as a kind of kaleidoscope effect — there are only a limited number of pieces of coloured glass in a kaleidoscope, but vast numbers of combinations and relationships that can be generated.

One more thing I want to mention. Last week I talked about work that was all genetics. This week, no genetics at all — we have no idea what the source of the variation in these animals is. Is it explicitly genetic, or is it environmental? It doesn’t matter in this paper — it’s a measure of the plasticity of the amphibian limb, and it’s almost certainly both genes and environment. It’s going to take deeper work on the genetics of Taricha, which doesn’t seem to be going on much, although there is some work on genomics. Maybe you can go on to become an amphibian evo-devo person and fill in that information!

Hey, if you want to talk about this paper some more, read it — it’s not freely accessible, although maybe you can find it on sci-hub, or for a limited time, I’ll make it available. I’ll have a livestream on Saturday at noon Central time to say more about it, come on by! You’ll be recovered from your New Year celebrations by then, I hope.

Meanwhile, here are a bunch of my lovely patrons. You can join them patreon dot com slash pzmyers for as little as a dollar a month, or you can help me out by clicking on the like or subscribe buttons down below. I’ll have another evo-devo video next week!

Frustrating morning in the lab

All right, I accomplished something this morning: I got all the juvenile spiders moved out of their cramped dirty vials and into bigger, much cleaner condos.

Unfortunately, my plan to photograph all of them so I can start documenting early pigment patterns (eventually to log changing — maybe — pigment patterns as they grow) was foiled by a series of problems: a) my camera battery was dying, b) the battery in the LED panel I use for extra illumination was completely dead, c) my lab is a shambles right now, and d) I forgot anyway that when spiders get a change of venue, they turn frantic and scamper all about. “This is not my beautiful house,” they cry, “where is that large collection of dead flies?” So no, I could not get beautiful photos. I posted a few attempts on Instagram, but gave up and just focused on getting everyone moved.

But tomorrow! a) camera battery is charged, & I’ll bring my backup battery, b) LED panel battery is charging now, c) lab will still be a mess, but I can work around it, and d) the spiders will have settled down and be resting in their new cobweb, so I can take my photos and also, as a reward, fling a fly into their web.