How to make a bat

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The relative length of bat forelimb digits has not changed in 50
million years. (a) Icaronycteris index, which is a 50-million-year-old bat fossil. (b) Extant adult
bat skeleton. The metacarpals (red arrows) of the first fossil bats are already
elongated and closely resemble modern bats. This observation is confirmed by
morphometric analysis of bat forelimb skeletal elements.

or•gan•ic | ôr’ganik | adjective. denoting a relation between elements of something such that they fit together harmoniously as necessary parts of a whole; characterized by continuous or natural development.

One of the wonderful things about how development works is that organisms function as wholes, and changes in one property trivially induce concordant changes in other properties. Tug on one element, changing it’s orientation or size, and during embryogenesis any adjacent elements make compensatory adjustments, so that the resultant form flows, fits, and looks organic. This isn’t that surprising a feature of development, though, unless you have the mistaken idea that the genome encodes a blueprint of morphology. It doesn’t; what it contains is a description of interacting agents that work together in a process to produce a complex result. Changes in genes and regulatory elements can essentially produce changes in rules of development, rather than crudely specifying blocks of morphology.

What does this mean for evolution? It means that subtle changes to the rules of development can be caused by small changes to genes (and especially, to regulatory regions of genes), and that the resulting morphological changes may be dramatic, but are still integrated organically into the form of the organism as a whole. Our understanding of how development works is making it clear that large scale macroevolutionary change may be much easier than we had thought.

Here’s an example where this insight is clarifying the evolution of an organism: the fossil record of bats shows an abrupt appearance of fairly sophisticated creatures with elongated digits, clearly capable of gliding or powered flight, with no known intermediates. We expect there were less fully flight-ready predecessors, but fossil preservation is not kind to small, delicate boned animals. It’s also possible that the transitional period was fairly brief; it looks like turning a paw into a long-fingered membranous wing may be a fairly simple change on a molecular level.

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Bat development

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It always gives a fellow a warm feeling to see an old comrade-in-arms publish a good paper. Chris Cretekos was a graduate student working on the molecular genetics of zebrafish at the University of Utah when I was a post-doc there, and he’s a good guy I remember well…so I was glad to see his paper in Developmental Dynamics. But then I notice it wasn’t on zebrafish—Apostate! Heretic!

Except…it’s on bats. How cool is that? And it’s on the embryonic development of bats. Even cooler! I must graciously forgive his defection from the zebrafish universe since he is working on an organism that is weird and fascinating and important.

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Catfish eating its dinner

John Lynch beat me to this story about catfish feeding on land, so I’ll be brief. It shows how the eel catfish, Channallabes apus, can manage to take an aquatic feeding structure and use it to capture terrestrial meals. Many fish rely on suction feeding: gape the mouth widely and drop the pharyngeal floor, and the resulting increase in volume of the oral cavity just sucks in whatever is in front of the animal. That doesn’t work well at all in the air, of course—try putting your face a few inches in front of a hamburger, inhale abruptly, and see how close you come to sucking in your meal. So how does an aquatically adapted feeder make the transition to eating on land?

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Malacology morning

My wife thought this story about left-handed snails having a competitive advantage, in that they seem to be better able to escape predation by right-handed crabs, was pretty cool. She also recalled that I’d scribbled up something about snail handedness before, so to jump on the bandwagon, I’ve brought those stories over from the old site.

The handedness of snail shells is a consequence of early spiral cleavages in the blastula. It’s a classic old story in developmental biology—everyone ought to know it!

There was also a story last year about shell chirality in Euhadra. There, it wasn’t a matter of predation, but a potential isolating mechanism, and one where mating compatibility and character displacement could play a role.

Everyone can read up on snails while I’m off at class this morning.

Chirality in Euhadra

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Since Coturnix turned me on to this paper on snail chirality in PLoS (pdf), I had to sit down and learn something new this afternoon.

Chirality is a fascinating aspect of bilaterian morphology. We have characteristic asymmetries—differences between the left and right sides of our bodies—that are prescribed by genetic factors. Snails are particularly interesting examples because snail shells have an obvious handedness, with either a left-(sinistral) or right-handed (dextral) twist, and that handedness derives from the arrangement of cell divisions very early in development.

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Spiral cleavage

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Developmental biologists are acutely interested in asymmetries in development: they are visible cues to some underlying regional differences. For instance, we’d like to know the molecules and interactions involved in taking a seemingly featureless sphere, the egg, and specifying one side to go on to form a head, and the the opposite side to form a tail. We’d like to understand why our back (or dorsal) side looks different from our belly (or ventral) side. One particularly intriguing distinction, though, is the left-right axis. For the most part, left and right are nearly identical, mirror-images of one another, but there are also key asymmetries. Your heart, for instance, is larger on the left side than the right, your liver lies mostly on the right side of your abdomen while the stomach arcs to the left, and these arrangements are essential for normal function. Left-right asymmetries are more subtle than anterior-posterior or dorsal-ventral differences, and that makes them especially fascinating.

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Tiktaalik makes another gap

Paleontologists have uncovered yet another specimen in the lineage leading to modern tetrapods, creating more gaps that will need to be filled. It’s a Sisyphean job, working as an evolutionist.

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This creature is called Tiktaalik roseae, and it was discovered in a project that was specifically launched to find a predicted intermediate form between a distinctly fish-like organism, Panderichthys, and the distinctly tetrapod-like organisms, Acanthostega and Ichthyostega. From the review article by Ahlberg and Clack, we get this summary of Tiktaalik‘s importance:

First, it demonstrates the predictive capacity of palaeontology. The Nunavut field project had the express aim of finding an intermediate between Panderichthys and tetrapods, by searching in sediments from the most probable environment (rivers) and time (early Late Devonian). Second, Tiktaalik adds enormously to our understanding of the fish-tetrapod transition because of its position on the tree and the combination of characters it displays.

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