Darwin was a gardener

Maybe you think it’s spring — I don’t, I just looked out through ice-glazed windows at half a foot of new snow — and you’re thinking about the garden. Here’s an idea: you don’t need to take a trip to the Galapagos to study evolution, you can do it right in your backyard. The New York Botanical Garden is opening a new exhibit, called Darwin’s Garden.

In all, the tour is 33 stops, spread throughout about half of the garden’s 250 acres. Visitors who enter the exhibition through the Enid A. Haupt Conservatory will encounter a replica of a room in Darwin’s house, designed so they can look through the window, as he did, to a profusion of plants and bright flowers: hollyhocks, flax and of course primroses, what Todd Forrest, the garden’s vice president for horticulture, calls “a typical British garden.” On a table stands a tray holding quills, brushes, sealing wax and tweezers, the kinds of simple tools Darwin used to conduct his world-shaking research.

Brilliant! Evolution is not something that requires exotic, out of the way locales and weird, obscure organisms to study — it’s everywhere.

Still just a lizard

Blogging on Peer-Reviewed Research

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The title gets the principal objection of any creationist out of the way: yes, this population of Podarcis sicula is still made up of lizards, but they’re a different kind of lizard now. Evolution works.

Here’s the story: in 1971, scientists started an experiment. They took 5 male lizards and 5 female lizards of the species Podarcis sicula from a tiny Adriatic island called Pod Kopiste, 0.09km2, and they placed them on an even tinier island, Pod Mrcaru, 0.03km2, which was also inhabited by another lizard species, Podarcis melisellensis. Then a war broke out, the Croatian War of Independence, which went on and on and meant the little islands were completely neglected for 36 years, and nature took its course. When scientists finally returned to the island and looked around, they discovered that something very interesting had happened.

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Basics: How can chromosome numbers change?

There in the foaming welter of email constantly flooding my in-box was an actual, real, good, sincere question from someone who didn’t understand how chromosome numbers could change over time — and he also asked with enough detail that I could actually see where his thinking was going awry. This is great! How could I not take time to answer?

So here’s the question:

How did life evolve from one (I suspect) chromosome to… 64 in horses, or whatever organism you want to pick. How is it possible for a sexually reproducing population of organisms to change chromosome numbers over time?

Firstly: there would have to be some benefit to the replication probability of the organisms which carry the chromosomes. I don’t see how this would work. How is having more chromosomes of any extra benefit to an organism’s replicative success? Yes, perhaps if those chromosomes were full of useful information… but the chances of that happening are non existent and fly in the face of ‘small adaptations over time’.

Secondly, the extra chromosomes need to come from somewhere. I’m not sure about this, but I believe chromosome number are not determined by genes, are they? There isn’t a set of genes which determines the number of chromosomes an organism has. So the number is fixed, determined by the sexually reproducing parents. Which leads me to believe that if the number does change, and by chance the organism is still alive and capable of sexual reproduction, that the number will start swinging back and forward, by 1 or 2, every generation, and never stabilising. The chances of this happening are also very very slim.

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Optical Allusions

Jay Hosler has a new book out, Optical Allusions(amzn/b&n/abe/pwll). If you’re familiar with his other books, Clan Apis(amzn/b&n/abe/pwll) and The Sandwalk Adventures(amzn/b&n/abe/pwll), you know what to expect: a comic book that takes its science seriously. Hosler has a fabulous knack for building serious content into a light and humorous medium, just the kind of approach we need to get wider distribution of science into the culture.

This one has a strange premise. Wrinkles the Wonder Brain is an animated, naked brain working for the Graeae Sisters, and he loses the one eye they share between them — so he has to go on a quest to recover it. I know, it sounds like a stretch, but it works in a weird sort of way, and once you start rolling with it, you’ll find it works. Using that scenario to frame a series of encounters, Wrinkles meets Charles Darwin and learns how evolution could produce something as complex as an eye; talks about the sub-optimal design of retinal circuitry with a cow superhero; discovers sexual dimorphism with a crew of stalk-eyed pirates; learns about development of the eye from cavefish and a cyclops; chats with Mr Sun about the physics of radiation; there are even zombie G proteins and were-opsins in a lesson about shape changing. This stuff is seriously weird, and kids ought to eat it up.

It isn’t all comic art, either. Each chapter is interleaved with a text section discussing the details — you can read the whole thing through, skipping the text (like I did…), and then go back and get more depth and directions for future reading in the science. This is a truly seditious strategy. Suck ’em in with the entertainment value, and then hand ’em enough substance that they might just start thinking like scientists.

It’s all good stuff, too. A colleague and I have been considering offering an interdisciplinary honors course in physics and biology with the theme of the eye, specifically for non-science majors, and this book has me thinking it might make for a good text. It’ll grab the English and art majors, and provide a gateway for some serious discussions that will satisfy us science geeks. I recommend it for you, too — if you have kids, you should grab all of Hosler’s books. Even if you don’t have kids, you’ll learn a lot.

Jay Hosler also explains the intent of the project, and you can read an excerpt.

The Sunday morning session at the Oregon evo-devo symposium

[Since I had to fly away early this morning and missed all these talks, I had to rely on regular commenter DanioPhD to fill in the gaps … so here’s her summary:]

This morning’s final series of talks each focused on a different phylum, but the unifying theme was one of bridging the processes of microevolution and macroevolution. The first talk after breakfast (and a long night of Scotch-drinkin’ and story-swappin’ prior to that) was Bernie Degnan of the University of Queensland. He summarized his work on Amphimedon queenslandica, a sponge species developed as a model of a representative primitive metazoan. Sponges diverged from the metazoan lineage ca. 700 MYA and possess the most minimalist metazoan body plan–no nervous system, muscles, nor any discernible tissues in the adult body architecture. Their embryos, however, feature robust anterioposterior patterning, distinct cell types organized into tissues, and cell morphogenesis typical of more complex metazoans. These embryonic characteristics are achieved by a regulatory network of genes, which, while inactive in the adult sponge, strongly support the presence of similar molecules in the ancestral metazoan genome. A few million years after the divergence of porifera, metazoans were able to co-opt these molecular toolkits to build the diverse, molecularly and morphologically distinct tissues common to all bilaterians. PZ has previously written up one such sponge tale here describing the molecular precursors to a nervous system in the sponge genome. Precursors to pretty much every other developmental ‘big gun’, e.g, Hox genes, Pax genes, Wnts, Hedgehog, etc. are also present as a basic prototype, in the Amphimedon genome.

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The afternoon session at the Oregon evo-devo symposium

I’m going to get off a quick summary of this afternoon’s talks, then I have to run down to the poster session to find out what the grad students have been doing. Are we having fun yet? I’m going to collapse in bed tonight, and then unfortunately I have to catch an early flight back home, so I’m going to miss a lot of cool stuff tomorrow.

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The morning session at the Oregon evo-devo symposium

My brain is most wonderfully agitated, which is the good thing about going to these meetings. Scientists are perverse information junkies who love to get jarred by new ideas and strong arguments, and meetings like this are intense and challenging. I’ve only got a little time here before the next session, so let me rip through a short summary of my morning.

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Coyne and Wray at the Oregon symposium on evo-devo

So here I am at the IGERT Symposium on Evolution, Development, and Genomics, having a grand time, even if I did get called out in the very first talk. There were two keynote talks delivered this evening, both of which I was anticipating very much, and which represented the really good side of science: two differing points of view wrestling with each other for consensus and for testable, discriminating differences. They also had dueling t-shirts.

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Quote of the week

Mike the Mad Biologist wins a gold star for this quote that I’ll be stealing:

The other thing we evolutionary biologists don’t do enough of, and this stems from the previous point, is make an emotional and moral case for the study of evolution. Last night, I concluded my talk with a quote from Dover, PA creationist school board member William Cunningham, who declared, “Two thousand years ago someone died on a cross. Can’t someone take a stand for him?”

My response was, “In the last two minutes, someone died from a bacterial infection. We take a stand for him.”

Now that is good framing.

Eppur si muove!

Blogging on Peer-Reviewed Research

The Harvard multimedia team that put together that pretty video of the Inner Life of the Cell has a whole collection of videos online (including Inner Life with a good narration.) Go watch the one titled F1-F0 ATPase; it’s a beautiful example of a highly efficient molecular motor, and it’s the kind of thing the creationists go ga-ga over. It’s complex, and it does the same rotary motion that the bacterial flagellum does; it has a little turbine in the membrane, a stream of protons drives rotation of an axle, and the movement of that axle drives conformation changes in the surrounding protein that promote the synthesis of ATP. It’s a molecular machine all right. Makes a fellow wonder if possibly it’s “irreducible”, doesn’t it?

Well, it’s not. It can be broken down further and it still retain that rotary motion.

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