Finding Fossils in Opaque Amber
Posted on April 2nd, 2008 by blue collar scientistHere’s a pretty clever scientific technique. Let’s say you’ve got a source of amber - lots of amber - and you want to check it for fossils. The problem, though - the amber is impure, or it has nonbiological inclusions, or it is badly scratched up - whatever the reason, you can’t see through it and can’t tell what is inside. It looks like this:

Researchers have come up with a pretty cool technique to get around this problem. They are x-raying it instead.
This may sound pretty obvious, but it isn’t. The surface texture of amber scatters x-rays like mad, and this makes it very difficult to get an image of what is inside. The researchers came up with a clever way around this. The density of amber ranges from 1.05 to 1.15 grams per cubic centimeter. That’s really close to water, at 0.998 grams per cubic centimeter. Since scattering occurs preferentially when electromagnetic radiation encounters a density variation, the researchers simply put their amber samples into water. The water flows into the scratches and fills them up, making the surface of the amber look a lot smoother to the x-rays than it otherwise would.
The researchers used a very specific imaging technique, with the winsome name propagation phase contrast microradiography. Someday, I hope to understand exactly how that works in x-rays, but I know about phase contrast micrography in optical wavelengths, and that’s a tangent I think is worth exploring. To do this in visible-light microscopes, you start with partially coherent light, and you shine it through a ring, and then focus it on your specimen with a condenser lens. Once it has gone through the specimen, it goes through the objective, and then passes through a ‘negative’ ring - instead of a piece of material that has a donut-shape cut out of it to let light through, this piece of material is a donut-shape that blocks light (but allows light through the donut hole as well as though the outside of the donut). Once the light passes through this apparatus, you focus it into an image, and you get a really weird effect. Diffraction converts small changes in the phase of the light into large differences in amplitude - or brightness. The result is that stuff you have a real hard time seeing any other way leaps out at you. It is such an impressive technique that its inventor, Frits Zernike, won the Nobel Prize for coming up with it. Nikon has an excellent discussion of the optical technique.
Presumably, the x-ray apparatus works on similar principles. In any case, they’ve come up with this:

The top image is a standard x-ray, while the bottom image utilizes the phase contrast technique. Amazing.
The scientists imaged 640 pieces of amber from the Charentes region in southwestern France. They discovered 356 fossil animals, going from wasps and flies, to ants or even spiders and acarians.
Acarians, by the way, are mites and ticks, and one of them that was found in the amber was only 0.8 millimeters in size. Quite impressive. And I really recommend you click over to the press release, which has lots of pictures well worth seeing. The researchers report they’ve been able to determine the families of 53% of the inclusions, in some cases from 3-dimensional images. I don’t know how that compares to optical techniques on transparent amber, but it is certainly good enough to be useful. The method could potentially shed a lot of light on the evolution of small arthropods.
There are two really cool things about this. The first is that most amber is opaque - 80% of it at Charentes, where the researchers took their samples. The second is that there’s probably lots of opaque amber sitting around in museums that has been kept because it is interesting for some reason or other. This amber can now be studied.
Want the original paper?
M. Lak, D. Néraudeau, A. Nel, P. Cloetens, V. Perrichot and P. Tafforeau, Phase contrast X-ray synchrotron imaging: opening access to fossil inclusions in opaque amber, Microscopy and Microanalysis, Forthcoming article, doi: 10.1017/S1431927608080264

