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Introduction:
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The thorax of a trilobite
(yellow in image left) is comprised of a number of separate segments, usually of similar shape
and varying somewhat in size, that articulate with each other and
with the posterior edge of the cephalon and the anterior edge of the pygidium, allowing the trilobite to bend upward and downward, and in many species, allowing the animal to enroll
as a protective behavior. As with all of the major parts of the dorsal
exoskeleton, each segment of the thorax bears a central axial lobe
between two symmetrical pleural lobes (right). Underneath the
animal, each thoracic segment bears a pair of legs and gills, but there
are also limbs under the cephalon and the pygidium.. The occipital segment (the posterior-most of the fused segments that make up the cephalon) and the anterior-most segment of the pygidium are morphologically most similar to the thoracic segments in many species of trilobites. This is partly a function of ontogeny, in which the pygidium releases thoracic segments forward during growth, and the functional constraints of the articulation of cephalon and pygidium with the first and last thoracic segments, respectively. This can be seen in the trilobites shown below, as well as variation in thoracic structure. |
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| Asaphiscus wheeleri |
Arctinurus boltoni |
Modocia laevinucha |
Calymene niagarensis |
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| Huntoniatonia oklahomensis | Olenellus gilberti | Reedops deckeri | Breviscutellum sp. |
In the images above, sometimes the similarity between the occipital
segment and the thoracic segments are striking. In Reedops deckeri, round lateral lobes on either side of the thoracic axis
are mirrored in not only the occipital lobe, but also the glabellar lobe
immediately anterior to it. The occipital segment of Modocia laevinucha
is partially defined by the posterior facial suture, which
further enhances the similarity between that cephalic segment and
the first thoracic segment. In Huntoniatonia oklahomensis, the pygidial segments look very much like fused thoracic segments. The spines of the pygidium of Arctinurus boltoni
are so similar to the backward-facing thoracic pleural spines that it
is difficult to tell where the thorax ends and the pygidium begins
(there are 11 thoracic segments and three pairs of pygidial spines).
A structural thoracic feature associated with enrollment is the pleural fulcrum,
where there is a clear change of angle from the near-horizontal inner
pleural region to a more steeply-sloped outer region. In the trilobites
above, the fulcrum is particularly apparent in Calymene, Reedops, and Breviscutellum, and is subtle or lacking in Olenellus, a primitive species that was not thought to enroll well.
Articulation structures
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images below detail some of the thoracic structures that
allow articulation and movement, and show how the separate
segments fit
neatly with each other, in a species for which articulation details have been well-studied. |
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![]() Ceraurinella typa (above) is a cheirurid
trilobite with 11 thoracic segments. The details of its thoracic
morphology are well known, and will be used here to demonstrate how
segments articulate with each other.
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![]() One thoracic segment, separated
from the others, shows the portion that is typically visible in light
brown, and structures that are usually at least partially
hidden by adjacent segments in other colors. Anterior of the axial ring is an
articulating half-ring (blue), that fits under the axial ring of the
neighboring segment. Similarly, there are anterior processes (knobs)
near the axis and near the fulcrum, that lie along an anterior flange (green).
These fit into sockets on the posterior flange (yellow) of the adjacent segment.(see below).
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![]() Seen from the side, the same
structures described at left are shown in matching colors. How these
fit with adjacent segments is shown below.
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![]() ![]() The same fit relationships are shown from the side here.
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| Schmalenseeia fusilis 0 segments |
Peronopsis interstricta 2 segments |
Elrathia kingi 13 segments |
Balcoracania dailyi 100+ segments |
Some references:
Chatterton, B.D.E. & M. Campbell. 1993. Enrolling in trilobites: A review and some new characters. Memoirs of the Association of Australian Paleontologists 15:103-23.
Harrington, H.J. 1959. General description of Trilobita: Thoracic region. In: Moore, R.C., ed. Treatise on Invertebrate Paleontology, Part O, Arthropoda 1. Geological Society of America & University of Kansas Press. Lawrence, Kansas & Boulder, Colorado. xix + 560 pp., 415 figs.
Hughes, N.C. 2003. Trilobite tagmosis and body patterning from morphological and developmental perspectives. Integrative and Comparative Biology 43(1):185-206.
Hughes, N.C. 2007. The evolution of trilobite body patterning. Annual Review of Earth and Planetary Sciences. 35:401-34.
Whittington, H.B. 1997. Morphology of the exoskeleton. In: Kaesler, R. L., ed. Treatise on Invertebrate Paleontology, Part O, Arthropoda 1, Trilobita, revised. Volume 1: Introduction, Order Agnostida, Order Redlichiida. The Geological Society of America, Inc. & The University of Kansas. Boulder, Colorado & Lawrence, Kansas. xxiv + 530 pp., 309 figs.
all figures above ©1999-2007 by S.M. Gon III created with Macromedia
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