Showing posts with label Anomalocaris. Show all posts
Showing posts with label Anomalocaris. Show all posts

Tuesday, March 31, 2009

Another Anomalocaris

ResearchBlogging.org
I don’t know! You wait ages for a new Anomalocarid, then two come by in close succession! First Schinderhannes bartelsi and now Hurdia.

Yes . . . well . . . another Anomalocarid,

Another weird Anomalocarid.

Allison C. Daley, Graham E. Budd, Jean-Bernard Caron, Gregory D. Edgecombe,, & Desmond Collins (2009). The Burgess Shale Anomalocaridid Hurdia and Its Significance for Early Euarthropod Evolution. Science, 1597-1600 DOI: 10.1126/science.1169514

Where to start! When I first saw it, I thought is was an Anomalocarid caught in flagrante delicto with a phyllocarid!

This is a bit of déjà vu, as with the original identification of Anomalocaris from the Burgess Shale, here’s another case of a number of isolated fragments being found previously (mouthparts, frontal appendages, body, and those weird frontal carapaces - a total of 8 Cambrian taxa) and given separate names, now being brought together into one complete specimen – just like the original Anomalocaris.

While the body, eyes and great appendages are similar to other Anomalocarids, the major difference here is the strange, and very large, carapace or shield-like structure on the head.

It is unlike any other Anomalocarid, with the possible exception of S. bartelsi which has a structure at the back of the head, which may be a funky posterior-flaring carapace-like structure (although that structure could be a pair of trunk appendages).

Fig. 2. Paratype specimen and isolated components of H. victoria. (A) ROM 49930, paratype, lateral view showing lateral flaps. (B) ROM 59258, frontal appendage morph A. (C) ROM 59259, frontal appendage morph B. (D) ROM 59260, mouthpart with extra teeth rows. (E) ROM 59261, lanceolate gill blades showing attachment at one end (arrow). (F) ROM 59262, paired P-elements. (G) USNM 57718, holotype of H. victoria. Scale bars, 1 cm. Abbreviations are as in Fig. 1. B, Banffia; ex, extra teeth rows.

Firstly the head. This is by far the most bizarre Anomalocarid, by virtue of the head, which is the first Anomalocarid identified with a carapace. At almost 50% of the length of the animal, it's huge, and made of two different "elements", a single “H” element and a paired “P” element. There doesn’t appear to be anything below this carapace, so it’s function is something of a mystery.

Why on earth is it there?!

Sexual selection maybe?
There are certainly examples of other arthropods that have an exaggerated body part used to attract a mate – think of the fiddler crab, but all seven fully articulated (with all the bits in the right place) specimens show this remarkable carapace, and it’s unlikely that all seven would be all one sex (if the structure was confined to one sex). Although it would be interesting to see if the size of the carapaces shows any bimodal distribution which may indicate a size differential, possibly based on sex. But as arthropods generally keep growing, maybe there are two sets of growth trends.

Prey capture maybe?
Perhaps Hurdia trapped small prey below the carapace and then advanced so that the appendages could grasp the prey. Or maybe it was used to dig into soft sediment after prey. Or perhaps it contained sensing apparatus to detect prey in the sediment

Who knows?

The rest of the beast conforms pretty much to the standard Anomalocarid body plan, including the circular jaws. This time, however, there are more teeth just for added effect.

Hurdia does have a fine set of gills though. And they appear to be free hanging gill structures, and similar to crustacean and chelicerate gill structures, rather than the modern arthropod biramous limb (where the leg and the gill are part of the same structure). This is interesting because it is thought that the Cambrian arthropod biramous limb formed by the fusion of a uniramous leg (just the leg) and a respiratory exite (gill), whereas the modern biramous limb is formed by a split of the main axis of the limb. The presence of separate filamentous gills in Cambrian Anomalocarids pushes the structure below the crown group arthropods and into the stem group arthropods, supporting the fusion theory.

An analysis groups Hurdia along with Anomalocaris and Laggania as a sister group, outside of the Euarthropods, or crown group arthropods.

Schinderhannes bartelsi fits in between Hurdia and Fuxianhuia.

Incidentally the reconstruction of Hurdia was done by Merrianne Collins, who did the reconstructions for Steve Gould's book on the Burgess Shale fossils, "Wonderful Life".

Allison C. Daley, Graham E. Budd, Jean-Bernard Caron, Gregory D. Edgecombe,, & Desmond Collins (2009). The Burgess Shale Anomalocaridid Hurdia and Its Significance for Early Euarthropod Evolution. Science, 1597-1600 DOI: 10.1126/science.1169514

Tuesday, March 10, 2009

Palaeoporn 11 - again


OK, back by huge public demand . . . err of one. Palaeoporn 11 is back with mark-ups.

The photo is of a portion of an Anomalocaris appendage, and shows the typical preservation style of fossils in the Emu Bay Shale.

In the photo (click to enlarge) there are three segments (S) and two segment boundaries (SB) the segment boundary is doubled because the original appendage was roughly circular, and when you flatten a tube, you don't get the appendage boundary matching up when squashed.

The specimen has been re-crystallised during an episode of overthrusting. The surface of the fossil is normal calcite, but in the centre the calicite is in the a fibrous form (FC). The matrix where the fossil was, is smooth (M2), the normal matrix is M1.

There is no phosphatisation of muscle tissue, and so this is probably a moult. But that's another story . . .

Sunday, March 8, 2009

Palaeoporn 11



A slightly different Palaeoporn this time, as there's a bit of a theme this week, on preservation. A bit later I'll be discussing how to fossilise muscle tissue. This, and other specimens helped in coming up with the process.

This is a fragment of an Anomalocaris appendage from the Cambrian Emu Bay Shale. The interesting thing is the preservation. The outer layer preserves the impression of the appendage, together with segment boundaries. Inside, is a layer of fibrous calcite crystals. The specimen has been re-crystallised after a metamorphic event which included overthrusting. The crystals are, in fact aligned to the stress field, as they 'lean' towards the north - the thrust direction was south to north.

Tuesday, February 10, 2009

More Devonian Anomalocaris

Thanks to John and Callan I now have a copy of the paper. It’s brief but interesting.

So lets have a look at Schinderhannes bartelsi from the Lower Devonian Hunsrück Slate.

S. bartelsi is a great appendage arthropod with radial jaws. Great appendage arthropods, as the name suggests, are a group of arthropods with big frontal appendages, which are not known after the Middle Cambrian. Some, like Anomalocaris had radial jaws, but most did not. It may be that the great appendage is homologous (or directly comparable) to the frontal appendages in chelicerates. So finding a great appendage arthropod in the Lower Devonian could be something of a missing link, if indeed the great appendage and chelicerate appendage is homologous.

In this instance, it is S. bartelsi's shared characters with Anomalocaris that are really interesting.
Fig. 1. Holotype of Schinderhannes bartelsi. (A) Ventral. (B) Interpretative drawing of ventral side. l, left; r, right; A1, great appendage; A2, flaplike appendage; sp, spine; fm, flap margin; te, tergite; ta, trunk appendage. (C) Partly exposed dorsal side, horizontally mirrored. (D) Interpretative drawing of dorsal side. (E) Interpretative drawing of great appendages, combining information from the dorsal and ventral sides. (F) Radiograph. (G) Reconstruction. Scale bar, 10 mm [for (A) to (G)]. (H) Mouth-part. Scale bar, 5 mm.

Appendages
2, spiny, check.
But the reconstruction has weird cross-linkages between the two appendages. What’s with that? It looks like the appendages have been tied together. This means that the appendages have no independent movement and must work as a locked pair. I’m not convinced of this interpretation. It might be that what is overlapping is the series of up to five or six regularly spaced orthogonal spines along the length of the main spines which are attached to most of the segments of the appendage. In other words the segments of the appendage have a large spine attached to it, which would point downwards if the appendage were stretched out in front of the head. These spines in turn have a smaller set of spines coming off the leading edge, kind of like a comb, with the backbone of the comb representing the large spine coming off the appendage segment, and the set of five or six smaller spines, the teeth of the comb.

They could be used as a net to trap small prey, or, more likely given that they are short, as a means of added grip to ensure the prey doesn’t get away once in the grasp of the appendages. But the bondage reconstruction doesn’t work for me (maybe I need to more adventurous?)

Eyes
2, massive, check
They are enormous! This means S. bartelsi was most probably a predator, possibly adapted for low light conditions, close to the bottom.

Mouth
1, radial, check.
This is the most interesting feature that really links S. bartelsi to Anomalocaris. Radial jaws are so rare, and while the one in S. bartelsi has a lot less plates that the traditional Anomalocaris, it’s hard to argue against S. bartelsi as being distantly related in some way to Anomalocaris. A great appendage on it’s own? Meh. But a great appendage AND a radial jaw? That's fairly convincing.

Highly specialised swimming appendage
2, weird, check
No, wait! Hang on! What? This is just too weird. Highly specialised swimming appendages on the trunk I could accept, but not attached to the head. That just will not work. We rarely have large, functioning, head appendages posterior of the mouth. Maybe if it was some weird rigid structure coming off the posterior margin of the head shield, then yeah, but you just can’t have your highly specialised swimming head appendages AND flap them.

They are most probably highly specialised appendages on the first trunk segment. This would explain the spines along the leading edge of the appendage (exopod flaps maybe?), and would allow them to move as the trunk appendaged are set up for movement. They may be highly modified flukes, such as those on the last but one trunk segment.

There's something wierd going on with the trunk appendages, but they are not well preseved, and the paper doesn't make much of them as it isn't critical to the classification.

100 Million year gap
The authors place S. bartelsi between Anomalocaris and the other arthropods, with some justification. So where did all the round mouthed great appendage arthropods go for 100 million years?

Well, as the paper suggests, preservation plays a role here. These great appendage arthropods tend to be only lightly mineralized, and so do not preserve in normal situations. They are generally found only in areas of exceptional preservation, which would limit the numbers of fossils as there are just too few decent sites with exceptional preservation.

Also competition with the new predators on the block (cephalopods, the new-fangled vertebrates, etc), may well have pushed these arthropods to marginal areas, reducing and restricting their distribution.

It is a great pity that there is only one specimen, and an even greater pity that the quarry where S. bartelsi was found has now closed.

One way to check to see if great appendage arthropods with radial jaws are around, is to find evidence of their attacks – they leave distinctive bite marks. Has anyone surveyed the Hunsrück Slate fossils for bite marks?

Gabriele Kühl, Derek E. G. Briggs, and Jus Rust. A Great-Appendage Arthropod with a Radial Mouth from the Lower Devonian Hunsrück Slate, Germany.
Science 323, 771 (2009). DOI: 10.1126/science.1166586

P.S. I note that Derek resisted the urge to reference Anomalocaris briggsi in the paper, which is a pity 'cos then I would have got a citation in Science!

P.P.S. I've just received word that there will be paper on a new "funky" Anomalocaris coming soon. Details when it's published.

Monday, February 9, 2009

Devonian Anomalocaris!?


Well, actually, no. But it got your attention!

What we have here is Schinderhannes bartelsi from the Devonian aged Hunsrück Slate, near Bundenbach in Germany.

The find is described in the latest issue of Science, but I haven't got a copy so I can't say too much yet, but I'll be writing more once I get hold of the paper.

The appendages (the ones up front, not the ones sticking out the sides making S. bartelsi look like Thunderbird 2) sure look like Anomalocaris appendages, but there is only so many ways you can do large frontal appendages before you start repeating them.

The real interesting thing is the mouth. There are lots of ways you can do jaws, but radial jaws are very rare.

I wonder if there are any examples of fossils with bite marks from the Hunsrück Slate?

There is a Science Daily story here.

The critter is approximately 4 inches long.

Honestly! I'd hardly finished banging on about how Anomalocaris was crucified on the spandrals of San Marco, when up pops S. bartelsi! Still, in my defence, S. bartelsi does look like it comes pre-crucified!

More soon.

Sunday, December 7, 2008

CSI Cambrian

[bum bum - bum - bum bum. Whooooo are you? - Who? Who? - Who? Who?]

Grissom: Well? What do we have?
Catherine: The deceased is a 0 foot 1 inch arthropod of uncertain gender
G: Hmm. Time of Death?
C: That’s proving a little difficult.
G: OK. Do we know how long the body has been there?
C: Best estimate is five hundred and nineteen million years.
G: [raises eyebrow]So not much left then?
C: Actually quite a lot. The lab guys say it’s in a lager statten.
G: Ah, Lagerstätten. An old German mining term meaning “mother lode”. Used by palaeontologists to mean a deposit with exceptional preservation. So we’re in luck.
C: Yeah . . . right .

G: Do we have a cause of death?
C: Oh I think so. Death would appear the result of a large wound in the right side. A significant piece of the right side has been removed, and is missing.
No sign of a struggle at the site either, so it would appear that the attack took place elsewhere and the victim ended up here.
G: Got a name?
C: Naraoia? Possibly. Difficult to say at this stage.

G: What was the victim wearing?
C: The typical Naraoid two piece, a short anterior shield and a longer posterior shield. Although the posterior shield is a bit more stylish than normal, as it sharply tapers towards the back.

G: Any suspects?
C: Well, we’ve liked Anomalocaris for this type of attack for a while now, but we’ve never been able to make a solid case.
G: Why?
C: Well, despite the fact that Anomalocaris is pretty much the largest organism around, and it has jaws that could have made the bite marks we see in a number of victims, we know that the jaws probably didn’t come together very strongly. They didn’t . . . um . . . occlude. They didn’t occlude. Also the jaws themselves were not strongly mineralised.
G: [Begins to speak] Scl . .
C: [interrupting, rolling her eyes] Sclerotised, they were poorly sclerotised. And so couldn’t bite into strongly mineralised or sclerotised attire.

G: OK. Lets review the evidence.
C: Well we have a naraoid with a large wound on the right side.
G: Anything else?
C:Well, there’s some minor damage of the opposite side to the large wound, but we can’t tell if that was caused at the same time as the major attack or if it is unrelated. Anomalocaris is a suspect, but doesn’t appear to have been able to inflict the damage we see.

G: Whatever caused the wound also cut through the cuticle. What does that tell us?
C: Well, first we need to know about the properties of the cuticle. Arthropod cuticle has a bilayered construction, consisting primarily of a thin, usually mineralised, outer exocuticle, underlain by a thicker, unmineralised, endocuticle. Each of these brings differing mechanical properties, with the hardened exocuticle strong (and thus resistive to cracking) under compression (or being poked), but weak (and vulnerable to cracking) under tensional forces (or being stretched). By comparison, the softer, more pliant endocuticle is the opposite, weak under compression, but strong under tension. These properties combine to provide a greater level of protection against mechanical attack than either layer could alone.
By varying the thickness and mineralization of the two layers, arthropods can produce a wide range of exoskeleton types, from highly plastic to highly rigid.

G: I’m impressed
C: Yeah, well, you have so many arthropods crawling around your office that I though I should read up on them.

G: And what does that mean for the properties of the cuticle under pressure?
C: Well, Highly plastic cuticle can deform almost to breaking point and rebound back to its original shape when the pressure is released, kind of like pushing your fingers into a balloon and then letting go.
G: Elastic deformation.
C: Right. While highly rigid cuticle will show almost no deformation until the moment it breaks, kind of like pushing down on a dinner plate.
G: Remind me never to invite you around for dinner.
C: Cute. But most cuticle is a compromise between highly elastic and highly rigid.
G: So?
C: That means under low pressure, the cuticle shows plastic deformation, which will rebound if the pressure is released. But, at a certain level of pressure, the cuticle reaction changes.
G: The yield point.
C: Right. If the pressure exceeds that level, any deformation is permanent, like pushing your fingers into plasticine.
G: And if the pressure continues to increase?
C: Eventually the cuticle will fail

G: [Grissom’s phone rings. He puts it on speaker.] Warrick. Right on time. What did you find?
W: Grissom. As you asked, I looked at all the cases that had with a similar MO to the one you have there.
G: And?
W: You were right. In a significant number of instances, the victims had damage on the opposite side to the major injury.
I’m sending through a couple of photos. The first is from the same location but the victim was a Redlichia. The second is from Canada and shows a similar MO, but in this case the victim was Ogygopsis..
I’ve also got an example from the Ordovician, where the attacker was identified as a nautiloid.
G: As yes, the first example of our squid overlords exercising their might.
W, C: What?
G: Oh nothing, just a blog I read. Thank you Warrick. [Hangs up]
C: Nautiloid? There are no nautiloids at this location. How does that help us.
G; It’s all evidence. And we know the MO of nautiloids, they wrap their tentacles around the body of the pray and force it into the mouth, where the strong beak bites down.
C: But we have already established that that MO wouldn’t work with Anomalocaris because of the poorly sclerotised jaws.
G: Correct. Now with that, and the nautiloid MO in mind, lets re-examine the victim.
C: OK. Well the pressure exerted on the right side was clearly enough to break the cuticle.
G: Agreed. Anything else?
C: Umm . . . wait a minute, the damage to the left side! It’s permanently deformed
G: So?
C: Since it occurs in a number of cases it probably occurred at the same time as the major damage. That means it’s has significant pressure applied to it, enough to exceed the yield point. Maybe the attacker had two goes at the victim?
G: Possible, but I don’t think so. The margin is pinched in. it doesn’t look like a bite mark.
C: Well if the damage was done by an appendage, where is the second site of damage? Anomalocaris has two appendages.
G: Take a close look at the Pposterior shield. See along the margin?
C: It’s thicker! The cuticle folds back on itself. It would have been much stronger than the anterior shield margin.
G: Correct. Also the posterior shield tapers quite markedly, so the best purchase would have been on the anterior shield.

G: OK what else do we know about Anomalocaris?
C: It has a strong muscular head with powerful frontal appendages. But that’s what I don’t understand!
G: What?
C: The whole powerful appendages thing. Why have them? If all you are doing is holding the victim to your mouth, you really don’t need such powerful appendages.
G: That’s a good question. Unless . .
C: Unless . . . unless . . . the head and appendages are doing something else . . . something powerful . . .
G: So it’s not just guiding the victim to the mouth, the appendages are applying real pressure to the other side. Why?
C: It can’t be that the attacker was applying considerable force just to position the victim in the mouth, because the mouth couldn’t bite down. The force had to be doing something else.
G: Go on.
C: Well, the powerful appendages and head muscles must have been doing something in tandem with the weak jaws, something that was powerful enough the break the cuticle.

G: What do we know about the cuticle that can help us here?
C: Well, we know that the two-layered construction is best able to withstand the stresses associated with the downward force that normal biting would produce.
Wait a minute. What if it were possible to reverse this?
G: What do you mean?
C: Well, the cuticle is set up to withstand a compressive force on the upper layer, which translates to an extensive force on the lower layer as it stretches around the point of impact.
What if this were reversed, and the extensive force were applied to the upper layer?
G: Interesting idea, but how would you do that?
C: We know that the appendages were doing something that provided enough force to damage the side opposite the major wound. Maybe it was flexing the victim back and forth, using the jaws as a pivot point.
G: Like you would do to break a credit card?
C: Exactly. You can’t break a credit card with your hands, but you can force it to crack by flexing it back and forth.
G: I think you may have something here. So what is your description of the events leading to the crime?
C: The victim is attacked from the right hand side by Anomalocaris, which grabs the victim on the left side of the body and feeds to right side into the jaws. It then flexes the victim back and forth, inducing a weakness, which eventually caused the cuticle to crack.
G: I think you’ve cracked the case!
[fade out]

Epilogue
[Grissom walks past Catherine’s office where she is sitting at her desk with her head in her hands]
G: Catherine?
C: I’ve just had a call from some lawyer at the Discovery Institute. They are challenging our findings on Anomalocaris.
G: On what grounds?
C: They say that, as the arthropod cuticle is so complex and perfectly suited to its purpose, it had to be designed. And, since we cannot know the mind of the Designer, He could have made that particular cuticle act that way.
G: He?
C: Yeah, I noticed that. Anyhow, they also said that our dogmatic commitment to the materialist world view was closing our mind to other possibilities and was prejudicing the case against Anomalocaris.
G: What did you say?
C: I told them that they could shove their religious, anti-science claptrap right up their[bum bum - bum - bum bum. Whooooo are you? - Who? Who? - Who? Who?]

Credits

Naraoia sp. - Itself
Redlichia takooensis - Itself
Ogygopsis klotzi - Itself
Anomalocaris - Itself

Collins, D. (1996) The "evolution of Anomalocaris and its classification in the arthropod Class Dinocardia (nov.) and Order Radiodonta (nov.). Journal of Paleontology, v. 70, pp. 280-293.

Saturday, November 1, 2008

PalaeoPorn 1


This is the type specimen of what I would later name Anomalocaris briggsi, in the field, 10 minutes after being exposed for the first time in about five hundred and nineteen million years. You couldn't wipe the smile of my face for the rest of that day! The coin is an Australian 20 cent piece, about the same size as a Canadian $2 coin. See below for a close up and a better guide to the size (the scale bar is 2 cm).