ETA: OK, technically it should be “suspension-feeding”, because there’s a good chance that its feeding mechanics involved more than simple filtering (see comments). I hate retconning, so I’ll leave the post as it is aside from this addendum. Thanks for the heads-up, Dave Bapst 🙂

This is when I put everything resembling work aside to squee madly over a fossil.

(Imagine me grinning like crazy and probably bouncing up and down a bit in my seat)

Tamisiocaris is a newly “updated” beast from the Cambrian, and the coolest thing I’ve seen since that helicoplacoid on a stalk (most cool things come from the Cambrian, right?). It is the Cambrian equivalent of a baleen whale.

Anomalocaridids were close relatives of arthropods and are among the most iconic creatures of the Cambrian. Most anomalocaridids we know of were large, swimming predators with large head appendages bearing sturdy spines to grab prey and bring it to that trilobite-crunching pineapple slice mouth. Going with the whale analogy, they were more like the killer whales of their time (although they would be easy snacks for an actual killer whale). In fact, when the putative head appendage of Tamisiocaris was originally described by Daley and Peel (2010), the only odd thing they noted about it was that it was not hardened or obviously segmented the way those of Anomalocaris were.*

Tamisiocaris was already cool back then, because it was the first animal of its kind found at Sirius Passet in Northern Greenland, one of the lesser known treasure troves of fabulous Cambrian fossils. However, since then, more appendages have been found, and it turns out that those long spines had been hiding a fascinating secret.

They were… kind of hairy.


Closer examination of the appendages shows that their long, slender spines bore closely spaced bristles, making each spine look like a fine comb (whole appendage and close-up of a spine above from Vinther et al. [2014]). With all the spines next to each other, the bristles would have formed a fine mesh suitable for catching prey smaller than a millimetre. Compared with modern filter-feeding animals, Tamisiocaris fits right in – it would have “fished” in a similar size range as a greater flamingo. Vinther et al. (2014) suggest that Tamisiocaris would have brought its appendages to its mouth (which isn’t among the known fossils) one at a time to suck all the yummies off.

These guys are tremendously interesting for more than one reason, as the new study points out. First, HOLY SHIT FILTER FEEDING ANOMALOCARIDIDS! (Sorry. I’m kind of excited about this.) Second, the mere existence of large**  filter feeders implies a richness of plankton people hadn’t thought existed at the time. Third, there is some remarkable convergent evolution going on here.

Often, really big plankton eaters evolve from really big predators – see baleen whales, basking sharks, and these humongous fish for example. It’s not an already filter-feeding animal growing bigger and bigger, it’s an already big animal taking up filter-feeding. The interrelationships of anomalocaridids suggest the same story played out among them – ferocious hunters begetting “gentle giants” in a group with a totally different body plan from big vertebrates. For all the dazzling variety evolution can produce, sometimes, it really rhymes.

And finally, Vinther et al. did something really cool that tickles my geeky side in a most pleasant way. In their phylogenetic analysis that they did to find out where in anomalocaridid evolution this plankton-eating habit came along, they found that Tamisiocaris was closely related to another anomalocaridid with (on a second look) not dissimilar appendages. They named the group formed by the two the cetiocarids – after an imaginary filter-feeding anomalocaridid created by artist John Meszaros for the awesome All Your Yesterdays project.

Man. That’s definitely worth some squee.


*Disclaimer: I’m basing this on the abstract only, since palaeontological journals are one of the unfortunate holes in my university library’s otherwise extensive subscriptions.

**For Cambrian values of “large” – based on the size of the appendages, this creature would have been something like two feet long.



Daley AC & Peel JS (2010) A possible anomalocaridid from the Cambrian Sirius Passet Lagerstätte, North Greenland. Journal of Palaeontology 84:352-355

Vinther J et al. (2014) A suspension-feeding anomalocarid from the Early Cambrian. Nature 507:496-499

So… much… STUFF!

Gods, this is what I’m faced with all the time. Someone needs to tell me how proper science bloggers pick articles to discuss, because I just get my RSS alerts, start squeeing, and end up not writing about anything because damn, I WANT TO WRITE ABOUT EVERYTHING!

I give up. I’ll just dump all the cool stuff that’s accumulated on my desktop and bookmark bar here and return to lengthy meandering whenever I don’t feel like I’ve been caught in a bloody tornado 😉

So, here is some Cool Stuff…

(1) A group measured the rate of DNA decay in 158 moa bones of known age from three sites. Really cool stuff, to go out and directly measure how ancient DNA disappears from dead things under more or less identical conditions. The unsurprising result is that DNA decays exponentially, a bit like radioactive material. This suggests that the main cause of the decay is random breaking of the strands. The surprising bit is that this happens much more slowly than previously estimated, suggesting that in ideal (read: frozen) conditions, it might be worth looking for preserved DNA in samples as old as a million years.

(On a side note, if you ever get a chance to see a talk by Eske Willerslev, one of the authors and a leading expert on ancient DNA, don’t miss it. The man is absolutely hilarious.)

– Allentoft ME et al. (2012) The half-life of DNA in bone: measuring decay kinetics in 158 dated fossils. Proceedings of the Royal Society B FirstCite article, available online 10/10/2012, doi: 10.1098/rspb.2012.1745

(2) The beaks of the finches, or mixing and matching developmental recipes. This study examines the genetic basis of beak shape in three little birds closely related to Darwin’s famous finches. The three finches, just like Darwin’s, share the same basic beak shape, only bigger or smaller. However, there seem to be two distinct developmental programs at work, using different genes and parts of the skeleton to orchestrate beak development. One of the three newly investigated species (the one most closely related to Darwin’s finches) apparently uses the same developmental program as its more famous relatives, even though its beak is shaped more like the other two birds studied here. I told you – genetics, development and homology are complicated 😉

– Mallarino R et al. (2012) Closely related bird species demonstrate flexibility between beak morphology and underlying developmental programs. PNAS 109:16222–16227

(3) Armoured fossil links worm-like molluscs to chitons. There’s a little-known group (or groups) of molluscs called aplacophorans that have only a coat of tiny spicules instead of shells and look more like worms than “proper” molluscs. Exactly where they fit into our picture of mollusc evolution has been controversial to say the least – they could represent an old lineage separate from other molluscs, they could be related to cephalopods, they could be related to chitons, they could be one group or they could be two lineages in completely different places on the tree… Well, a new fossil named Kulindroplax seems to argue for the chiton connection: the animal has the characteristic armour plates of a chiton on an aplacophoran-like body. Similar creatures have been discovered before, but this guy with its detailed 3D preservation provides the clearest evidence of the link so far.

– Sutton MD et al. (2012) A Silurian armoured aplacophoran and implications for molluscan phylogeny. Nature 490:94-97

(4) More cool fossils – this time straight from my beloved Cambrian. Nereocaris, a newly described Burgess Shale arthropod, suggests to its discoverers that the earliest arthropods weren’t predators prowling the seafloor, but swimmers who might have been filter feeders and certainly weren’t predators. The animal has a bivalved shell around its front end, similar to many other Cambrian swimming arthropods, and a long abdomen with paddles at the end. It bears the arthropod hallmark of a hardened and jointed exoskeleton, but it lacks specialised limbs such as antennae or mouthparts. In a cladistic analysis of arthropods and their nearest relatives, the new species comes out on the first branch within true arthropods, and the next few branches as we move towards living arthropods all contain similar shelled, swimming creatures. Since the non-arthropods closest to the real thing (i.e. anomalocaridids) were also fin-tailed swimmers, this arrangement makes the transition between them and true arthropods smoother than previously thought. It also suggests that the hard exoskeleton so characteristic of arthropods originally functioned in swimming – perhaps as an anchor for swimming muscles.

– Legg DA et al. (2012) Cambrian bivalved arthropod reveals origin of arthrodization. Proceedings of the Royal Society B FirstCite article, available online 10/10/2012, doi: 10.1098/rspb.2012.1958


And … there was also

… but it’s almost bedtime, and if I wanted to summarise every one of those, I’d be here all weekend 😦

See, this is why being a science nerd today is both amazing and frustrating. There’s just so. Much. Stuff.

Anomalocaris is watching you!

With thirty thousand tiny eyes…

(Image above by Craig Dylke of Art Evolved)

The Cambrian Emu Bay Shale of Australia is something of an eye mine, it seems. After a previous paper on beautiful fossils of Emu Bay arthropod eyes (Lee et al., 2011), scientists now report the exquisitely preserved compound eyes of none other than the iconic Cambrian predator, Anomalocaris.

(Any excuse to post pictures of Anomalocaris is a good excuse 😛 This one is also Craig Dylke’s, and shows Anomalocaris on the hunt among a shoal of small arthropods.)

We’ve known for a long time that anomalocaridids (close relatives of arthropods) had well-developed eyes, but previously published fossils didn’t include details like individual facets. The three eyes (one pair and a loner) described in Paterson et al. (2011) clearly show thousands upon thousands of tiny, tightly packed hexagonal facets.

Each eye had over 16 000 little lenses, and the authors suspect that many more could have been destroyed in the process of flattening a bulb-shaped object into a two-dimensional fossil. In life, the gaze of Anomalocaris may have been just as unsettling – and its vision just as sharp – as that of a living dragonfly. Except this guy could grow longer than your leg.

(Oh hai? Dragonfly by Arturo Nikolai, from Wikimedia Commons)

The eyes were found without a body, but their shape is a good match for less well-preserved anomalocaridid eyes that were still attached to the animal. Also, being around an inch wide at their widest, they are way too big for anything else known from the Emu Bay fossil beds.

So it seems anomalocaridids hunted with some of the sharpest eyes of any arthropod, living or extinct. As if they weren’t badass enough already 😀

(Also, wow, the same team made Nature with their Cambrian eyes twice in the same year.)



Lee MSY et al. (2011) Modern optics in exceptionally preserved eyes of Early Cambrian arthropods from Australia. Nature 474:631-634

Paterson JR et al. (2011) Acute vision in the giant Cambrian predator Anomalocaris and the origin of compound eyes. Nature 480:237-240