An extinction event is a widespread and rapid decrease in the biodiversity on Earth. Such an event is identified by a sharp change in the diversity and abundance of multicellular organisms. It occurs when the rate of extinction increases with respect to the background extinction rate and the rate of speciation. Estimates of the number of major mass extinctions in the last 540 million years range from as few as five to more than twenty. These differences stem from disagreement as to what constitutes a "major" extinction event, and the data chosen to measure past diversity.
The PaleozoicEra is the first of three geological eras of the Phanerozoic Eon. Beginning 538.8 million years ago (Ma), it succeeds the Neoproterozoic and ends 251.9 Ma at the start of the Mesozoic Era. The Paleozoic is subdivided into six geologic periods :
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 extant trilobites finally 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.
The Late Ordovician mass extinction (LOME), sometimes known as the end-Ordovician mass extinction or the Ordovician-Silurian extinction, is the first of the "big five" major mass extinction events in Earth's history, occurring roughly 443 Mya. It is often considered to be the second-largest known extinction event, in terms of the percentage of genera that became extinct. Extinction was global during this interval, eliminating 49–60% of marine genera and nearly 85% of marine species. Under most tabulations, only the Permian-Triassic mass extinction exceeds the Late Ordovician mass extinction in biodiversity loss. The extinction event abruptly affected all major taxonomic groups and caused the disappearance of one third of all brachiopod and bryozoan families, as well as numerous groups of conodonts, trilobites, echinoderms, corals, bivalves, and graptolites. Despite its taxonomic severity, the Late Ordovician mass extinction did not produce major changes to ecosystem structures compared to other mass extinctions, nor did it lead to any particular morphological innovations. Diversity gradually recovered to pre-extinction levels over the first 5 million years of the Silurian period.
Dicynodontia is an extinct clade of anomodonts, an extinct type of non-mammalian therapsid. Dicynodonts were herbivores that typically bore a pair of tusks, hence their name, which means 'two dog tooth'. Members of the group possessed a horny, typically toothless beak, unique amongst all synapsids. Dicynodonts first appeared in Southern Pangaea during the mid-Permian, ca. 270–260 million years ago, and became globally distributed and the dominant herbivorous animals in the Late Permian, ca. 260–252 Mya. They were devastated by the end-Permian Extinction that wiped out most other therapsids ca. 252 Mya. They rebounded during the Triassic but died out towards the end of that period. They were the most successful and diverse of the non-mammalian therapsids, with over 70 genera known, varying from rat-sized burrowers to elephant-sized browsers.
Phacopida ("lens-face") is an order of trilobites that lived from the Late Cambrian to the Late Devonian. It is made up of a morphologically diverse assemblage of taxa in three related suborders.
Ptychopariida is a large, heterogeneous order of trilobite containing some of the most primitive species known. The earliest species occurred in the second half of the Lower Cambrian, and the last species did not survive the Ordovician–Silurian extinction event.
Proetida is an order of trilobite that lived from the Ordovician to the Permian. It was the last order of trilobite to go extinct, finally dying out in the Permian-Triassic extinction event.
Phillipsiidae is a family of proetid trilobites, the various genera of which comprise some of the last of the trilobites, with a range that extended from the Kinderhookian epoch of the Lower Mississippian, to the end of Changhsingian age at Permian-Triassic extinction event in the latest Permian period.
Cyamella is a genus of proetid trilobites. It was originally described by Robert M. Owens in 1978, as "Cyamops", a junior homonym of the fly genus Cyamops, but was renamed in 1990.
Cyclopygidae is a family of asaphid trilobites from the Ordovician. Cyclopygids had an extratropical distribution, and there is evidence that they lived in darker parts of the water column. Cyclopygids are characterized by enlarged eyes, with a wide angle of view, both horizontal and vertical, reminiscent of the eyes of dragonflies. These typically touch the glabella directly on the side. Cyclopygids all lack genal spines, but Symphysops carries a forward directed frontal spine on the glabella. It is presumed that at least the members of the genus Pricyclopyge swam upside down and had bioluminescent organs on the third thorax segment. Cyclopygids had between 7 and 5 thorax segments, a wide and stout axis, and short side lobes.
Proetus is a genus of proetid trilobite found in Silurian-aged marine strata of Europe.
Nipponaspis is a genus of proetid trilobite belonging to the family Phillipsiidae. Fossils of the various species are found in Middle Permian-aged marine strata of Fukushima Prefecture, Japan, China, Korea, and Alaska.
Thaiaspis is a genus of proetid trilobite belonging to the family Phillipsiidae. Fossils of the various species are found in Middle to Late Mississippian-aged marine strata of eastern Asia, especially of Carboniferous-aged marine strata in Thailand.
Vidria vespa is a proetid trilobite belonging to the family Phillipsiidae. The fossils are found in Middle Permian-aged marine strata of Western Texas. It is unique among Permian-aged trilobites in having a posterior spine emanating from the pygidium of the adult.
Gitarra is a genus of trilobite in the family Proetidae that lived between the late Tournaisian and Late Westphalian of the Lower-Middle Devonian.
Gerastos is a genus of proetid trilobite in the family Proetidae that lived between the Pragian and Eifelian of the Lower-Middle Devonian, spanning approximately 21 million years.
Ditomopyge is an extinct genus of trilobite belonging to the family Proetidae. It was extant during the Carboniferous and Permian and is widely distributed, with fossils found in Europe, southwest Asia, southeast Asia, Australia, North America, and South America.
Ameura is an extinct genus of trilobite belonging to the family Proetidae. Fossils from the genus have been found in late Paleozoic beds in North America.
Anisopyge is an extinct genus of trilobite belonging to the order Proetida and family Phillipsiidae. Specimens have been found in Permian beds in North and Central America.
