trilobite n : an extinct arthropod that was abundant in Palaeozoic times; had an exoskeleton divided into three parts

English

Etymology

tri- 'three' + lobe + -ite

Pronunciation

(US) /ˈtraɪləˌbaɪt/

Noun

1. an extinct arthropod of the class Trilobita, whose body had three large lobes

Translations

French

Noun

fr-noun m

1. Trilobite

Italian

Noun

1. Trilobite

Trilobites ("three-lobes") are extinct arthropods that form the class Trilobita. They appeared in the Middle Cambrian epoch and flourished throughout the lower Paleozoic era before beginning a drawn-out decline to extinction when, during the Late Devonian extinction, all trilobite orders, with the sole exception of Proetida, died out. The last of the trilobites disappeared in the mass extinction at the end of the Permian about 250 million years ago (m.y.a.).

Trilobites are very well-known, and possibly the second-most famous fossil group, after the dinosaurs. When trilobites appear in the fossil record of the Lower Cambrian they are already highly diverse and geographically dispersed. Because of their diversity and an easily fossilized exoskeleton, they left an extensive fossil record with some 17,000 known species spanning Paleozoic time. Trilobites have been important in biostratigraphy, paleontology, and plate tectonics research. For example, trilobites have been important in estimating the rate of speciation during the period known as the Cambrian Explosion because they are the most diverse group of metazoans known from the fossil record of the early Cambrian (Lieberman, 1999), and are readily distinguishable because of complex and well preserved morphologies. The trilobites are often placed within the arthropod subphylum Schizoramia within the superclass Arachnomorpha (equivalent to the Arachnata) (e.g., Cotton & Braddy 2004), although several alternative taxonomies are found in the literature.

Different trilobites made their living in different ways. Some led a benthic life as predators, scavengers or filter feeders. Some swam (a pelagic lifestyle) and fed on plankton. Still others (particularly the family Olenidae) are thought to have evolved a symbiotic relationship with sulfur-eating bacteria from which they derived food.

Phylogeny

Despite their rich fossil record with thousands of genera found throughout the world, the taxonomy and phylogeny of trilobites have many uncertainties. The systematic division of trilobites into nine distinct orders is represented by a widely held view that will inevitably change as new data emerge. Except possibly for the members of order Phacopida, all trilobite orders appeared prior to the end of the Cambrian. Most scientists believe that order Redlichiida, and more specifically its suborder Redlichiina, contains a common ancestor of all other orders, with the possible exception of the Agnostina. While many potential phylogenies are found in the literature, most have suborder Redlichiina giving rise to orders Corynexochida and Ptychopariida during the Lower Cambrian, and the Lichida descending from either the Redlichiida or Corynexochida in the Middle Cambrian. Order Ptychopariida is the most problematic order for trilobite classification. In the 1959 Treatise on Invertebrate Paleontology, what are now members of orders Ptychopariida, Asaphida, Proetida, and Harpetida were grouped together as order Ptychopariida; subclass Librostoma was erected in 1990 by Fortey (1990) to encompass all of these orders, based on their shared ancestral character of a natant (unattached) hypostome. The most recently recognized of the nine trilobite orders, Harpetida, was erected in 2002. The progenitor of order Phacopida is unclear.

Physical description

The bodies of trilobites are divided into three parts (tagmata): a cephalon (head), composed of the two preoral and first four postoral segments completely fused together; a thorax composed of freely articulating segments; and a pygidium (tail) composed of the last segments fused together with the telson. The pygidia are fairly rudimentary in the most primitive trilobites. The thorax is fairly flexible—fossilised trilobites are often found enrolled (curled up) like modern woodlice for protection. Trilobites are described based on the pydigium being micropygous (pydigium smaller than cephalon), isopygous (pydigium equal in size to cephalon), or macropygous (pydigium larger than cephalon).

Trilobite exoskeletons bear a variety of small-scale structures, such as nodes, ridges, tubercles and spines, collectively called prosopon. Alimentary ridge networks may have been either digestive or respiratory tubes in the cephalon and other regions (Clarkson, 1979). Early Cambrian trilobites have thin cuticles in which the alimentary networks can easily be seen. Trilobites had a single pair of preoral antennae and otherwise undifferentiated biramous limbs. Each exopodite (walking leg) had six segments, homologous to other early arthropods. The first segment also bore a feather-like epipodite, or gill branch, which was used for respiration and, in some species, swimming. The limbs were covered by the lateral projections of the dorsal exoskeleton called pleural lobes, extending outward from a central axial lobe.

Although trilobites were only armored on top, they still had a fairly heavy exoskeleton, composed of calcite and calcium phosphate minerals in a protein lattice of chitin. Unlike other groups of armored arthropods, which resorb most of their skeletal minerals prior to molting, a trilobite would cast off a fully mineralized molt. Thus a single trilobite animal could potentially have left multiple well-mineralized skeletons behind -- contributing to the abundance of trilobites in the fossil record. During molting, the exoskeleton generally split between the head and thorax, which is why so many trilobite fossils are missing one or the other. In most groups there were facial sutures on the cephalon to facilitate molting. The cheeks (genae) of the cephalon of trilobites, except some sightless species, supported a pair of compound eyes. The earliest trilobite known from the fossil record is the genus Fallotaspis within Order Redlichiida, dated to some (Fortey, 2000) .<--- Laudo Correctum 12/15/07 BLS. Other early genera include Profalloptaspis and Eofallotaspis, all appearing about the same time.

Even the earliest trilobites had complex, compound eyes with lenses made of calcite, a unique characteristic of all trilobite eyes. This confirms that eyes of arthropods and probably other animals were already quite developed at the beginning of the Cambrian. Improving eyesight of both predator and prey in marine environments probably provided one of the evolutionary pressures furthering an apparent rapid development of new life forms during what is known as the Cambrian Explosion.

Some trilobites such as those of the order Lichida evolved elaborate spiny forms, from the Ordovician until the end of the Devonian period. Examples of these specimens have been found in the Hamar Laghdad Formation of Alnif in Morocco. Collectors of this material should be aware of a serious counterfeiting and fakery problem with much of the Moroccan material that is offered commercially. Spectacular spined trilobites have also been found in western Russia; Oklahoma, USA; and Ontario, Canada. These spiny forms could possibly have been a defensive response to the evolutionary appearance of fish.

According to New Scientist magazine (May 2005), "some... trilobites... had horns on their heads similar to those of modern beetles." Based on the size, location, and shape of the horns, Rob Knell, a biologist at Queen Mary, University of London and Richard Fortey of London's Natural History Museum, concluded that the most likely use of the horns was combat for mates, making trilobites the earliest exemplars of this behavior. While this study only considered members of the Asaphida family Raphiophoridae, the conclusions are likely to be applicable to other trilobites as well, such as in the Phacopid trilobite Walliserops trifurcatus that had prominent horn-like spines on its cephalon.

Trilobites range in length from one millimeter to 72 cm (1/25 inch to 28 inches), with a typical size range of two to seven centimeters (1 to 3½ inches). The world's largest trilobite, Isotelus rex, was found in 1998 by Canadian scientists in Ordovician rocks on the shores of Hudson Bay.

Sensory organs

Many trilobites had eyes; they also had antennae that perhaps were used for taste and smell. Some trilobites were blind, probably living too deep in the sea for light to reach them. As such, they became secondarily blind in this branch of trilobite evolution. Others, such as Phacops rana, had eyes that were quite large for use in more well lit, predator-filled waters.

The eyes of trilobites were made of calcite (calcium carbonate, CaCO3). Pure forms of calcite are transparent, and some trilobites used a single crystallographically oriented, clear calcite crystal to form each lens of each of their eyes. In this, they differ from most other arthropods, which have soft or chitin-supported eyes. The rigid calcite lenses of a trilobite eye would have been unable to accommodate to a change of focus like the soft lens in a human eye would; however, in some trilobites the calcite formed an internal doublet structure, giving superb depth of field and minimal spherical aberration, as rediscovered by Dutch physicist Christiaan Huygens many millions of years later. A living species with similar lenses is the brittle star Ophiocoma wendtii.

The trilobite eyes were typically compound, with each lens being an elongated prism. The number of lenses in such an eye varied, however: some trilobites had only one, and some had thousands of lenses in a single eye. In these compound eyes, the lenses were typically arranged hexagonally.

Holochroal eyes

Holochroal eyes had a great number of (tiny) lenses (sometimes over 15,000), and are found in all orders of trilobite. These lenses were packed closely together (hexagonally) and touch each other. A single corneal membrane covered all lenses. These eyes had no sclera, the white layer covering the eyes of most modern arthropods.

Schizochroal eyes

Schizochroal eyes typically had fewer (and larger) lenses (to around 700), and are found only in Phacopida. The lenses were separate, with each lens having an individual cornea which extended into a rather large sclera.

Abathochroal eyes

Abathochroal eyes had around 70 small lenses, and are found only in Cambrian Eodiscina. Each lens was separate and had an individual cornea. The sclera was separate from the cornea, and did not run as deep as the sclera in schizochroal eyes.

Development

Trilobites grew through successive molt stages called "instars", in which existing segments increased in size and new trunk segments appeared at a sub-terminal generative zone during the "anamorphic" phase of development. The molt itself, is called ecdysis. This was followed by the "epimorphic" developmental phase, in which the animal continued to grow and molt, but no new trunk segments were expressed in the exoskeleton. The combination of anamorphic and epimorphic growth consistutes the "hemianamorphic" developmental mode that is common among many living arthropods. Trilobite development was unusual in the way in which articulations developed between segments, and changes in the development of articulation gave rise to the conventionally recognized developmental phases of the trilobite life cycle, which are not readily compared with those of other arthropods. The earliest trilobite growth stages known with certainty are of the protaspid stage, in which all segments were fused into a single shield comprising a cephalic (head) and trunk regions. In subsequent molt stages an articulation appeared between the head and the trunk, which marked the onset of the "meraspid" phase of development. At the onset of the meraspid phase the animal had a two-part structure - the head and the plate of fused trunk segments, called the pygidium. During the meraspid phase, new segments appeared near the rear of the pygidium as additional articulations developed at the anterior of the pygidium, releasing freely articulating thoracic segments. The "holaspid' phase of grow commenced when a stable, mature number of segments had been released into the thorax. Molting continued during the holaspid stage, with no changes in thoracic segment number. Onset of the holaspid phase and the epimorphic phase was coincident in some, but not all, trilobites. Some trilobites showed a marked transition in morphology at one particular instar, which has been called trilobite metamorphosis. Trilobite juveniles are reasonably well known and provide an important aid in evaluating high-level phylogenetic relationships among trilobites.

Terminology

When describing differences between different taxa of trilobites, the presence, size, and shape of the cephalic features above are often mentioned.

Figure 1 shows gross morphology of the cephalon. The cheeks (genae) are the pleural lobes on each side of the axial feature, the glabella. When trilobites molted or died, the librigenae (the so-called "free cheeks") often separated, leaving the cranidium (glabella + fixigenae) exposed. Figure 2 shows a more detailed view of the cephalon.

Origins

Based on morphological similarities, it is possible that the trilobites have their ancestors in arthropod-like creatures such as Spriggina, Parvancorina, and other trilobitomorphs of the Ediacaran period of the Precambrian. There are many morphological similarities between early trilobites and other Cambrian arthropods known from the Burgess Shale, the Maotianshan shales at Chengjiang and other fossiliferous locations. These are investigated further here: http://www.trilobites.info/triloclass.htm It is reasonable to assume that the trilobites share a common ancestor with these other arthropods prior to the Ediacaran-Cambrian boundary. Ancestral trilobites may have been somewhat soft bodied and developed their thick carapaces through Cuticularisation. As with other forms of trilobite body evolution, this was a defensive measure.

Extinction

The reason for the extinction of the trilobites is not clear, although it may be no coincidence that their numbers began to decrease with the appearance of the first sharks and other early gnathostomes in the Silurian and their subsequent rise in diversity during the Devonian period. Trilobites may have provided a rich source of food for these new animals. A smaller extinction event in the Middle Cambrian of trilobite orders possessing alimentary prosopon and a micropygidium may have been linked to the rise of cephalopods. Trilobites were under great selective pressure to develop defensive bodies quickly. The most radical change in body form occurred in the Middle Cambrian. As a means of defense, surviving orders developed isopygidius or macropygius bodies. This enabled trilobites to curl their bodies into a ball as a means of defense. A micropygidius trilobite cannot completely protect itself in a curled position with a pygidium smaller than the cephalon. It is analogous to pleurodirian (side-necked) turtles of the present day (Holocene). A terrestrial side neck could never evolve because the exposed neck in a side withdraw state would be vulnerable to a predator. Surviving trilobites developed thicker cuticles (as mentioned earlier) and as such, the alimentary prosopon are no longer visible due to the thickness. This makes an excellent fossil stratigraphic marker of the Cambrian period: Researchers who find trilobites with alimentary prosopon, and a micropygium, have found Early Cambrian strata (Schnirel, 2001).

After the mid-Cambrian extinction event, the next great extinction event occurred at the Frasnian - Famennian boundary at the end of the Devonian period. All orders (except one) of Trilobites became extinct. Trilobites were bottlenecked into one single order, the Proetida. This single order survived for millions of years, continued through the Carboniferous period and lasted to the great extinction event at the end of the Permian (where the vast majority of species on earth were wiped out). It is unknown why Order Proedita alone, survived.

Additionally, their relatively low numbers and diversity at the end of the Permian no doubt contributed to their extinction during that great mass extinction event. Foreshadowing this, the Ordovician mass extinction, though somewhat less substantial than the Permian one, also seems to have significantly narrowed trilobite diversity.

The closest extant relatives of trilobites may be the horseshoe crabs, according to Fortey (2000), or the cephalocarids, according to Lambert (1985).

Fossil distribution

Trilobites appear to have been exclusively marine organisms, since the fossilized remains of trilobites are always found in rocks containing fossils of other salt-water animals such as brachiopods, crinoids, and corals. Within the marine paleoenvironment, trilobites were found in a broad range from extremely shallow water to very deep water. The tracks left behind by trilobites crawling on the sea floor are occasionally preserved as trace fossils. These same trace fossils are also found in freshwater environments, suggesting either that some freshwater trilobites existed, or that the tracks are also made by other organisms. Trilobites, like brachiopods, crinoids, and corals, are found on all modern continents, and occupied every ancient ocean from which fossils have been collected.

Trilobite fossils are found worldwide, with many thousands of known species. Because they appeared quickly in geological time, and moulted like other arthropods, trilobites serve as excellent index fossils, enabling geologists to date the age of the rocks in which they are found. They were among the first fossils to attract widespread attention, and new species are being discovered every year. Some Native Americans, recognizing that trilobites were water creatures, had a name for them which means "little water bug in the rocks".

A famous location for trilobite fossils in the United Kingdom is Wren's Nest, Dudley in the West Midlands, where Calymene blumenbachi is found in the Silurian Wenlock Group. This trilobite is featured on the town's coat of arms and was named the "Dudley locust" or "Dudley bug" by quarrymen who once worked many of the now abandoned limestone quarries. Other trilobites found there include Dalmanites, Trimerus, Bumastus and Balizoma. Llandrindod Wells, Powys, Wales, is another famous trilobite location.

Spectacular trilobite fossils, showing soft body parts like legs, gills and antennae, have been found in British Columbia (Burgess Shale Cambrian fossils, and similar localities in the Canadian Rockies); New York State (Odovician Walcott-Rust Quarry, near Utica, N.Y., and the Beecher Trilobite Beds, near Rome, N.Y.), in China (Burgess Shale-like Lower Cambrian trilobites in the Maotianshan shales near Chengjiang), Germany (the Devonian Hunsrück Slates near Bundenbach, Germany) and, much more rarely, in trilobite-bearing strata in Utah and Ontario.

Trilobites are collected commercially in Russia (especially in the St. Petersburg area), Germany, Morocco's Atlas Mountains, (where a burgeoning trade in faked trilobites is also under way), Utah, Ohio, British Columbia, and in other parts of Canada.

Gallery

Proetid trilobites from Morocco

See also

• Prehistoric life
• List of trilobites

References

• Clarkson, E.N. (1993), ''Invertebrate Paleontology and Evolution. 4th Edition. Chapman/Hall, N.Y..
• Cotton, T.J., and S.J. Braddy. 2004. The phylogeny of arachnomorph arthropods and the origins of the Chelicerata. Transactions of the Royal Society of Edinburgh: Earth Sciences, 94: 169–193
• Trilobite! - Richard Fortey (2000) (ISBN 0-00-257012-2)
• David Lambert and the Diagram Group. The Field Guide to Prehistoric Life. New York: Facts on File Publications, 1985. ISBN 0-8160-1125-7
• Riccardo Levi-Setti. Trilobites. University of Chicago Press, 1993.
• A Guide to the Orders of Trilobite by Sam Gon III - an excellent, well-researched site with information covering trilobites from all angles. Includes many line drawings and photographs.
• Earliest combatants in sexual contests revealed from "New Scientist" magazine.
• The Trilobite papers
• Lieberman, BS, (1999) Testing the Darwinian Legacy of the Cambrian Radiation Using Trilobite Phylogeny and Biogeography Journal of Paleontology, 73(2)
• Tripp, RP, JT Temple, and KC Gass, (1977) The Silurian Trilobite Encrinurus variolaris and Allied Species, with Notes on Frammia, Palaeontology, 20(4)
• Fortey RA. 2001. Trilobite systematics: The last 75 years. Journal of Paleontology 75:1141–1151.
• Ebach, M.C. & K.J. McNamara. 2002. A systematic revision of the family Harpetidae (Trilobita). Records of the Western Australian Museum 21:135-67.
• The Virtual Fossil Museum - Class Trilobita - Including extensive photographs organized by taxonomy and locality.
• Kaesler RL, ed. 1997. Treatise on Invertebrate Paleontology, Part O, Volume 1, revised, Trilobita. Geological Society of America and University of Kansas Press, Lawrence, Kansas.
• Schnirel, B.L.(2001). Trilobite Evolution and Extinction., Graves Museum of Natural History, Dania, Florida.

External links

• Western Trilobite Association
• Kevin's Trilobite Gallery - a collection of photographs of trilobite fossils
• A Guide to the Orders of Trilobites
• Canadian trilobite web site: photographs of trilobite fossils
• The Paleontological Society