The hypostome is the hard mouthpart of trilobites found on the ventral side of the cephalon (head). The hypostome can be classified into three types based on whether they are permanently attached to the rostrum or not and whether they are aligned to the anterior dorsal tip of the glabella.
The center of the hypostome is an ovoid, typically convex part called the median body, often divided into an anterior lobe and a posterior lobe. Either side of the median body is a border with various extensions, including anterior and posterior wings, sometimes bearing knob-like processes. The hypostome is hollow, and encloses the mouthparts, the anterior digestive tract, and the bases of the antennae. Trilobite antennae pass through notches between the anterior and posterior wings, then forward. The anterior wings are designed to rest firmly against internal structures (ventral apodemes) on the glabella. [1]
Variation in trilobite hypostome morphology is crucial in modern discussions of trilobite phylogeny. [2] [3] Functional interpretations of hypostome shape also allow for reasonable speculation on the feeding habits of trilobite species. [4]
Although hypostome morphology is highly variable, three broad types are generally recognized:
A natant hypostome is not attached to the anterior doublure, with support assumed to be provided by a non-mineralised membrane. Natant hypostomes appear to have been conservative over the course of the evolution of trilobites [2] with overall form and shape of a simple ovoid without posterior extensions or ornamentation. [1] Natant hypostomes are thought to be ancestral to other hypostome forms [2] and thought to belong to trilobites with generalized particle feeding habits (i.e. little need to modify mouth-parts to deal with specialized food items). [4]
A conterminant hypostome is attached to the anterior doublure, aligned with the front edge of the glabella and found on trilobites thought of as predators. Anchoring the hypostome against the anterior doublure and cephalon provides structural bracing against which to tear apart prey. Different specializations of hypostome form might reflect different kinds of prey, or different feeding behaviors. [4]
An impendent hypostome is attached to the anterior doublure but not aligned with the front edge of the glabella. Many impendent hypostomes have prongs, grooves and other adaptations thought to relate to feeding on complex food sources. [4]
Trilobites are extinct marine arthropods that form the class Trilobita. Trilobites form one of the earliest known groups of arthropods. The first appearance of trilobites in the fossil record defines the base of the Atdabanian stage of the Early Cambrian period and they flourished throughout the lower Paleozoic before slipping into a long decline, when, during the Devonian, all trilobite orders except the Proetida died out. The last trilobites disappeared in the mass extinction at the end of the Permian about 251.9 million years ago. Trilobites were among the most successful of all early animals, existing in oceans for almost 270 million years, with over 22,000 species having been described.
Redlichiida is an order of trilobites, a group of extinct marine arthropods. Species assigned to the order Redlichiida are among the first trilobites to appear in the fossil record, about halfway during the Lower Cambrian. Due to the difficulty to relate sediments in different areas, there remains some discussion, but among the earliest are Fallotaspis, and Lemdadella, both belonging to this order. The first representatives of the orders Corynexochida and Ptychopariida also appear very early on and may prove to be even earlier than any redlichiid species. In terms of anatomical comparison, the earliest redlichiid species are probably ancestral to all other trilobite orders and share many primitive characters. The last redlichiid trilobites died out before the end of the Middle Cambrian.
Phacopidae is a family of phacopid trilobites that ranges from the Lower Ordovician to the Upper Devonian, with representatives in all paleocontinents.
Dalmanites is a genus of trilobite in the order Phacopida. They lived from the Late Ordovician to Middle Devonian.
Paradoxides is a genus of large to very large trilobite found throughout the world during the Middle Cambrian period. One record-breaking specimen of Paradoxides davidis, described by John William Salter in 1863, is 37 cm (15 in). The cephalon was semicircular with free cheeks ending in long, narrow, recurved spines. Eyes were crescent shaped providing an almost 360° view, but only in the horizontal plane. Its elongate thorax was composed of 19–21 segments and adorned with longish, recurved pleural spines. Its pygidium was comparatively small. Paradoxides is a characteristic Middle-Cambrian trilobite of the 'Atlantic' (Avalonian) fauna. Avalonian rocks were deposited near a small continent called Avalonia in the Paleozoic Iapetus Ocean. Avalonian beds are now in a narrow strip along the East Coast of North America, and in Europe.
Emuellidae are a small family of trilobites, a group of extinct marine arthropods, that lived during the late Lower Cambrian of the East Gondwana supercontinent, in what are today South-Australia and Antarctica.
Deiphon is a distinctive genus of Silurian phacopid trilobites of the family Cheiruridae found in Western and Central Europe, and in Central and Eastern United States. The type species, D. forbesi, from England, Bohemia, and Sweden, was discovered and described by the French paleontologist, Joachim Barrande in 1850.
Olenoides was a trilobite from the Cambrian period. Its fossils are found well-preserved in the Burgess Shale in Canada. It grew up to 10 cm long.
Asaphus is a genus of trilobites that is known from the Lower and Middle Ordovician of northwestern Europe.
Dikelocephalus is a genus of very large trilobites of up to 50 cm (20 in) long, that lived during the last 3 million years of the Cambrian (Sunwaptan). Their fossils are commonly found as disarticulated sclerites, in the upper Mississippi Valley and in Canada (Alberta). The exoskeleton is rounded anteriorly, with the thorax and sides of the tailshield slightly tapering to about 2⁄3× of the width across the base of the spines at the back of the headshield. At the side corners of the pygidium there may be triangular or hooked spines, pointing backwards, while between the spines the posterior margin is at a 30-75° angle with the lateral margin, gently convex or nearly straight. If pygidial spines are lacking, the margin is gradually rounded. The thorax has 12 segments.
Tsunyidiscus is a trilobite belonging to the suborder Eodiscina. Tsunyidiscus appeared near the end of the Lower Cambrian, during the late Atdabanian stage of geologic time and some collections suggest it may have survived into the Botomian. The genus is very small, oculate and isopypous with a narrow dome-shaped glabella and a narrow bullet-shaped pygidial axis. Thorax consists of three segments. Tsunyidiscus is the only genus currently attributed to the family Tsunyidiscidae.
The cephalon is the head section of an arthropod. It is a tagma, i.e., a specialized grouping of arthropod segments. The word cephalon derives from the Greek κεφαλή (kephalē), meaning "head".
Buenaspis is a genus of small nektaspid arthropod, that lived during the early Cambrian period. Fossil remains of Buenaspis were collected from the Lower Cambrian Sirius Passet Lagerstätte of North Greenland. Buenaspis looks like a soft eyeless trilobite. It has a headshield slightly larger than the tailshield (pygidium), and in between them six thoracic body segments (somites). The genus is monotypic, its sole species being Buenaspis forteyi.
Conocoryphe is a genus of primarily eyeless trilobites belonging to the family Conocoryphidae. They lived during the Middle Cambrian period, about 505 million years ago. These arthropods lived on the sea bottom (epifaunal) and lived off dead particulate organic matter.
Odontochile is a genus of trilobites in the order Phacopida, family Dalmanitidae.
Eodiscina is trilobite suborder. The Eodiscina first developed near the end of the Lower Cambrian period and became extinct at the end of the Middle Cambrian. Species are tiny to small, and have a thorax of two or three segments. Eodiscina includes six families classified under one superfamily, Eodiscoidea.
Psychopyge is a genus of trilobite, that lived during the upper Emsian and has been found in Germany and Morocco. It is characterized by the swordlike extension from the front of the head.
Viaphacops is a genus of trilobites in the order Phacopida, family Phacopidae, that lived during the Middle Devonian, and is known from North and South America, Asia.
Librostoma is a subclass of trilobites defined by having a natant hypostome, which is a hypostome that is free from the anterior doublure and aligned with the anterior of the glabella, this is unlike a conterminant hypostome, which is attached to the exoskeleton.
Waukeshaaspis is an extinct genus of trilobite known from the lower Silurian aged Waukesha Biota. A single species is currently known, Waukeshaaspis eatonae, which is known from strata belonging to the Telychian aged Brandon Bridge Formation in Wisconsin. Originally discovered alongside the Waukesha Biota in 1985, this genus wouldn't be properly described until 2024. Currently, this genus is placed within the family Dalmanitidae, within the larger Phacopida, which lasted from the Lower Ordovician to the Upper Devonian.