Ordovician

Last updated
Ordovician
486.85 ± 1.5 – 443.1 ± 0.9 Ma
Mollweide Paleographic Map of Earth, 465 Ma (Darriwilian Age).png
A map of Earth as it appeared 465 million years ago during the Middle Ordovician Epoch
Chronology
Etymology
Name formalityFormal
Name ratified1960
Usage information
Celestial body Earth
Regional usageGlobal (ICS)
Time scale(s) usedICS Time Scale
Definition
Chronological unit Period
Stratigraphic unit System
First proposed by Charles Lapworth, 1879
Time span formalityFormal
Lower boundary definition FAD of the Conodont Iapetognathus fluctivagus
Lower boundary GSSPGreenpoint section, Green Point, Newfoundland, Canada
49°40′58″N57°57′55″W / 49.6829°N 57.9653°W / 49.6829; -57.9653
Lower GSSP ratified2000 [5]
Upper boundary definitionFAD of the Graptolite Akidograptus ascensus
Upper boundary GSSP Dob's Linn, Moffat, U.K.
55°26′24″N3°16′12″W / 55.4400°N 3.2700°W / 55.4400; -3.2700
Upper GSSP ratified1984 [6] [7]
Atmospheric and climatic data
Sea level above present day180 m; rising to 220 m in Caradoc and falling sharply to 140 m in end-Ordovician glaciations [8]

The Ordovician ( /ɔːrdəˈvɪʃi.ən,-d-,-ˈvɪʃən/ or-də-VISH-ee-ən, -doh-, -VISH-ən) [9] is a geologic period and system, the second of six periods of the Paleozoic Era, and the second of twelve periods of the Phanerozoic Eon. The Ordovician spans 41.6 million years from the end of the Cambrian Period 486.85 Ma (million years ago) to the start of the Silurian Period 443.1 Ma. [10]

Contents

The Ordovician, named after the Welsh tribe of the Ordovices, was defined by Charles Lapworth in 1879 to resolve a dispute between followers of Adam Sedgwick and Roderick Murchison, who were placing the same rock beds in North Wales in the Cambrian and Silurian systems, respectively. [11] Lapworth recognized that the fossil fauna in the disputed strata were different from those of either the Cambrian or the Silurian systems, and placed them in a system of their own. The Ordovician received international approval in 1960 (forty years after Lapworth's death), when it was adopted as an official period of the Paleozoic Era by the International Geological Congress.

Life continued to flourish during the Ordovician as it had in the earlier Cambrian Period, although the end of the period was marked by the Ordovician–Silurian extinction events. Invertebrates, namely molluscs and arthropods, dominated the oceans, with members of the latter group probably starting their establishment on land during this time, becoming fully established by the Devonian. The first land plants are known from this period. The Great Ordovician Biodiversification Event considerably increased the diversity of life. Fish, the world's first true vertebrates, continued to evolve, and those with jaws may have first appeared late in the period. About 100 times as many meteorites struck the Earth per year during the Ordovician compared with today in a period known as the Ordovician meteor event. [12] It has been theorized that this increase in impacts may originate from a ring system that formed around Earth at the time. [13]

Subdivisions

In 2008, the ICS erected a formal international system of subdivisions for the Ordovician Period and System. [14] Pre-existing Baltoscandic, British, Siberian, North American, Australian, Chinese, Mediterranean and North-Gondwanan regional stratigraphic schemes are also used locally. [15]

Global/regional correlation

Approximate correlation of Ordovician regional series and stages [16]
ICS series ICS stage British seriesBritish stageNorth American seriesNorth American stageAustralian stageChinese stage
Upper Ordovician Hirnantian Ashgill Hirnantian CincinnatianGamachianBolindian Hirnantian
Katian RawtheyanRichmondianChientangkiangian
Cautleyan
PusgillianMaysvillianEastonianNeichianshanian
Caradoc StreffordianEdenian
CheneyanMohawkianChatfieldian
Sandbian BurrellianGisbornian
Turinian
Aurelucian
Whiterockian
Middle Ordovician Darriwilian LlanvirnLlandeilo Darriwilian Darriwilian
Abereiddian
Arenig Fennian
Dapingian Yapeenian Dapingian
WhitlandianRangerianCastlemainian
Lower Ordovician Floian IbexianBlackhillsianChewtonianYiyangian
Bendigonian
Moridunian
TuleanLancefieldian
Tremadocian Tremadoc MigneintianXinchangian
Stairsian
Cressagian
Skullrockian
Warendan

British stages and ages

The Ordovician Period in Britain was traditionally broken into Early (Tremadocian and Arenig), Middle (Llanvirn (subdivided into Abereiddian and Llandeilian) and Llandeilo) and Late (Caradoc and Ashgill) epochs. The corresponding rocks of the Ordovician System are referred to as coming from the Lower, Middle, or Upper part of the column.

The Tremadoc corresponds to the ICS's Tremadocian. The Arenig corresponds to the Floian, all of the Dapingian and the early Darriwilian. The Llanvirn corresponds to the late Darriwilian. The Caradoc covers the Sandbian and the first half of the Katian. The Ashgill represents the second half of the Katian, plus the Hirnantian.

Ashgill

The Ashgill Epoch, the last epoch of the British Ordovician, is made of four ages: the Hirnantian Age, the Rawtheyan Age, the Cautleyan Age, and the Pusgillian Age. These ages make up the time period from c. 450 Ma to c. 443 Ma.

The Rawtheyan, the second last of the Ashgill ages, was from c. 449 Ma to c. 445 Ma. It is in the Katian Age of the ICS's Geologic Time Scale.

Paleogeography and tectonics

Paleogeographic map of the Earth in the early Ordovician, 480 million years ago Earth Paleogeography 480 Ma (Early Ordovician, Tremadocian).png
Paleogeographic map of the Earth in the early Ordovician, 480 million years ago
Paleogeographic map of the Earth in the middle Ordovician, 470 million years ago Earth Paleogeography 470 Ma (Early-Middle Ordovician, Dapingian).png
Paleogeographic map of the Earth in the middle Ordovician, 470 million years ago
Paleogeographic map of the Earth in the late Ordovician, 450 million years ago Earth Paleogeography 450 Ma (Late Ordovician, Katian).png
Paleogeographic map of the Earth in the late Ordovician, 450 million years ago

During the Ordovician, the southern continents were assembled into Gondwana, which reached from north of the equator to the South Pole. The Panthalassic Ocean, centered in the northern hemisphere, covered over half the globe. [17] At the start of the period, the continents of Laurentia (in present-day North America), Siberia, and Baltica (present-day northern Europe) were separated from Gondwana by over 5,000 kilometres (3,100 mi) of ocean. These smaller continents were also sufficiently widely separated from each other to develop distinct communities of benthic organisms. [18] The small continent of Avalonia had just rifted from Gondwana and began to move north towards Baltica and Laurentia, opening the Rheic Ocean between Gondwana and Avalonia. [19] [20] [21] Avalonia collided with Baltica towards the end of Ordovician. [22] [23]

Other geographic features of the Ordovician world included the Tornquist Sea, which separated Avalonia from Baltica; [18] the Aegir Ocean, which separated Baltica from Siberia; [24] and an oceanic area between Siberia, Baltica, and Gondwana which expanded to become the Paleoasian Ocean in Carboniferous time. The Mongol-Okhotsk Ocean formed a deep embayment between Siberia and the Central Mongolian terranes. Most of the terranes of central Asia were part of an equatorial archipelago whose geometry is poorly constrained by the available evidence. [25]

The period was one of extensive, widespread tectonism and volcanism. However, orogenesis (mountain-building) was not primarily due to continent-continent collisions. Instead, mountains arose along active continental margins during accretion of arc terranes or ribbon microcontinents. Accretion of new crust was limited to the Iapetus margin of Laurentia; elsewhere, the pattern was of rifting in back-arc basins followed by remerger. This reflected episodic switching from extension to compression. The initiation of new subduction reflected a global reorganization of tectonic plates centered on the amalgamation of Gondwana. [26] [18]

The Taconic orogeny, a major mountain-building episode, was well under way in Cambrian times. [27] This continued into the Ordovician, when at least two volcanic island arcs collided with Laurentia to form the Appalachian Mountains. Laurentia was otherwise tectonically stable. An island arc accreted to South China during the period, while subduction along north China (Sulinheer) resulted in the emplacement of ophiolites. [28]

The ash fall of the Millburg/Big Bentonite bed, at about 454 Ma, was the largest in the last 590 million years. This had a dense rock equivalent volume of as much as 1,140 cubic kilometres (270 cu mi). Remarkably, this appears to have had little impact on life. [29]

There was vigorous tectonic activity along northwest margin of Gondwana during the Floian, 478 Ma, recorded in the Central Iberian Zone of Spain. The activity reached as far as Turkey by the end of Ordovician. The opposite margin of Gondwana, in Australia, faced a set of island arcs. [18] The accretion of these arcs to the eastern margin of Gondwana was responsible for the Benambran Orogeny of eastern Australia. [30] [31] Subduction also took place along what is now Argentina (Famatinian Orogeny) at 450 Ma. [32] This involved significant back arc rifting. [18] The interior of Gondwana was tectonically quiet until the Triassic. [18]

Towards the end of the period, Gondwana began to drift across the South Pole. This contributed to the Hibernian glaciation and the associated extinction event. [33]

Ordovician meteor event

The Ordovician meteor event is a proposed shower of meteors that occurred during the Middle Ordovician Epoch, about 467.5 ± 0.28 million years ago, due to the break-up of the L chondrite parent body. [34] It is not associated with any major extinction event. [35] [36] [37] A 2024 study found that craters from this event cluster in a distinct band around the Earth, and that the breakup of the parent body may have formed a ring system for a period of about 40 million years, with frequent falling debris causing these craters. [13]

Geochemistry

External mold of Ordovician bivalve showing that the original aragonite shell dissolved on the sea floor, leaving a cemented mold for biological encrustation (Waynesville Formation of Franklin County, Indiana). Anomalodonta gigantea Waynesville Franklin Co IN.JPG
External mold of Ordovician bivalve showing that the original aragonite shell dissolved on the sea floor, leaving a cemented mold for biological encrustation (Waynesville Formation of Franklin County, Indiana).

The Ordovician was a time of calcite sea geochemistry in which low-magnesium calcite was the primary inorganic marine precipitate of calcium carbonate. [38] Carbonate hardgrounds were thus very common, along with calcitic ooids, calcitic cements, and invertebrate faunas with dominantly calcitic skeletons. Biogenic aragonite, like that composing the shells of most molluscs, dissolved rapidly on the sea floor after death. [39] [40]

Unlike Cambrian times, when calcite production was dominated by microbial and non-biological processes, animals (and macroalgae) became a dominant source of calcareous material in Ordovician deposits. [41]

Climate and sea level

The Early Ordovician climate was very hot, [42] with intense greenhouse conditions and sea surface temperatures comparable to those during the Early Eocene Climatic Optimum. [43] Carbon dioxide levels were very high at the Ordovician period's beginning. [44] By the late Early Ordovician, the Earth cooled, [45] giving way to a more temperate climate in the Middle Ordovician, [46] with the Earth likely entering the Early Palaeozoic Ice Age during the Sandbian, [47] [48] and possibly as early as the Darriwilian [49] or even the Floian. [45] The Dapingian and Sandbian saw major humidification events evidenced by trace metal concentrations in Baltoscandia from this time. [50] Evidence suggests that global temperatures rose briefly in the early Katian (Boda Event), depositing bioherms and radiating fauna across Europe. [51] The early Katian also witnessed yet another humidification event. [50] Further cooling during the Hirnantian, at the end of the Ordovician, led to the Late Ordovician glaciation. [52]

The Ordovician saw the highest sea levels of the Paleozoic, and the low relief of the continents led to many shelf deposits being formed under hundreds of metres of water. [41] The sea level rose more or less continuously throughout the Early Ordovician, leveling off somewhat during the middle of the period. [41] Locally, some regressions occurred, but the sea level rise continued in the beginning of the Late Ordovician. Sea levels fell steadily due to the cooling temperatures for about 3 million years leading up to the Hirnantian glaciation. During this icy stage, the sea level has risen and dropped somewhat. Despite much study, the details remain unresolved. [41] In particular, some researches interpret the fluctuations in sea level as pre-Hibernian glaciation, [53] but sedimentary evidence of glaciation is lacking until the end of the period. [23] There is evidence of glaciers during the Hirnantian on the land we now know as Africa and South America, which were near the South Pole at the time, facilitating the formation of the ice caps of the Hirnantian glaciation.

As with North America and Europe, Gondwana was largely covered with shallow seas during the Ordovician. Shallow clear waters over continental shelves encouraged the growth of organisms that deposit calcium carbonates in their shells and hard parts. The Panthalassic Ocean covered much of the Northern Hemisphere, and other minor oceans included Proto-Tethys, Paleo-Tethys, Khanty Ocean, which was closed off by the Late Ordovician, Iapetus Ocean, and the new Rheic Ocean.


Life

A diorama depicting Ordovician flora and fauna Nmnh fg09.jpg
A diorama depicting Ordovician flora and fauna

For most of the Late Ordovician life continued to flourish, but at and near the end of the period there were mass-extinction events that seriously affected conodonts and planktonic forms like graptolites. The trilobites Agnostida and Ptychopariida completely died out, and the Asaphida were much reduced. Brachiopods, bryozoans and echinoderms were also heavily affected, and the endocerid cephalopods died out completely, except for possible rare Silurian forms. The Ordovician–Silurian extinction events may have been caused by an ice age that occurred at the end of the Ordovician Period, due to the expansion of the first terrestrial plants, [54] as the end of the Late Ordovician was one of the coldest times in the last 600 million years of Earth's history.

Fauna

Endoceras, one of the largest predators of the Ordovician Endoceras life restoration.png
Endoceras , one of the largest predators of the Ordovician
Fossiliferous limestone slab from the Liberty Formation (Upper Ordovician) of Caesar Creek State Park near Waynesville, Ohio. LibertyFormationSlab092313.jpg
Fossiliferous limestone slab from the Liberty Formation (Upper Ordovician) of Caesar Creek State Park near Waynesville, Ohio.
The trilobite Isotelus from Wisconsin Isotelus trilobite from Wisconsin.jpg
The trilobite Isotelus from Wisconsin

On the whole, the fauna that emerged in the Ordovician were the template for the remainder of the Palaeozoic. The fauna was dominated by tiered communities of suspension feeders, mainly with short food chains. The ecological system reached a new grade of complexity far beyond that of the Cambrian fauna, which has persisted until the present day. [41] Though less famous than the Cambrian explosion, the Ordovician radiation (also known as the Great Ordovician Biodiversification Event) [18] was no less remarkable; marine faunal genera increased fourfold, resulting in 12% of all known Phanerozoic marine fauna. [55] Several animals also went through a miniaturization process, becoming much smaller than their Cambrian counterparts.[ citation needed ] Another change in the fauna was the strong increase in filter-feeding organisms. [56] The trilobite, inarticulate brachiopod, archaeocyathid, and eocrinoid faunas of the Cambrian were succeeded by those that dominated the rest of the Paleozoic, such as articulate brachiopods, cephalopods, and crinoids. Articulate brachiopods, in particular, largely replaced trilobites in shelf communities. Their success epitomizes the greatly increased diversity of carbonate shell-secreting organisms in the Ordovician compared to the Cambrian. [57]

Aegirocassis, a large filter-feeding hurdiid radiodont from Morocco 20191205 Aegirocassis benmoulai Aegirocassis benmoulae.png
Aegirocassis , a large filter-feeding hurdiid radiodont from Morocco

Ordovician geography had its effect on the diversity of fauna; Ordovician invertebrates displayed a very high degree of provincialism. [58] The widely separated continents of Laurentia and Baltica, then positioned close to the tropics and boasting many shallow seas rich in life, developed distinct trilobite faunas from the trilobite fauna of Gondwana, [59] and Gondwana developed distinct fauna in its tropical and temperature zones. [60] The Tien Shan terrane maintained a biogeographic affinity with Gondwana, [61] and the Alborz margin of Gondwana was linked biogeographically to South China. [62] Southeast Asia's fauna also maintained strong affinities to Gondwana's. [63] North China was biogeographically connected to Laurentia and the Argentinian margin of Gondwana. [64] A Celtic biogeographic province also existed, separate from the Laurentian and Baltican ones. [65] However, tropical articulate brachiopods had a more cosmopolitan distribution, with less diversity on different continents. During the Middle Ordovician, beta diversity began a significant decline as marine taxa began to disperse widely across space. [66] Faunas become less provincial later in the Ordovician, partly due to the narrowing of the Iapetus Ocean, [67] though they were still distinguishable into the late Ordovician. [68]

Pentecopterus, the earliest known eurypterid, and found in Iowa Eurypterids Pentecopterus Vertical.jpg
Pentecopterus , the earliest known eurypterid, and found in Iowa

Trilobites in particular were rich and diverse, and experienced rapid diversification in many regions. [69] Trilobites in the Ordovician were very different from their predecessors in the Cambrian. Many trilobites developed bizarre spines and nodules to defend against predators such as primitive eurypterids and nautiloids while other trilobites such as Aeglina prisca evolved to become swimming forms. Some trilobites even developed shovel-like snouts for ploughing through muddy sea bottoms. Another unusual clade of trilobites known as the trinucleids developed a broad pitted margin around their head shields. [70] Some trilobites such as Asaphus kowalewski evolved long eyestalks to assist in detecting predators whereas other trilobite eyes in contrast disappeared completely. [71] Molecular clock analyses suggest that early arachnids started living on land by the end of the Ordovician. [72] Although solitary corals date back to at least the Cambrian, reef-forming corals appeared in the early Ordovician, including the earliest known octocorals, [73] [74] corresponding to an increase in the stability of carbonate and thus a new abundance of calcifying animals. [41] Brachiopods surged in diversity, adapting to almost every type of marine environment. [75] [76] [77] Even after GOBE, there is evidence suggesting that Ordovician brachiopods maintained elevated rates of speciation. [78] Molluscs, which appeared during the Cambrian or even the Ediacaran, became common and varied, especially bivalves, gastropods, and nautiloid cephalopods. [79] [80] Cephalopods diversified from shallow marine tropical environments to dominate almost all marine environments. [81] Graptolites, which evolved in the preceding Cambrian period, thrived in the oceans. [82] This includes the distinctive Nemagraptus gracilis graptolite fauna, which was distributed widely during peak sea levels in the Sandbian. [83] [23] Some new cystoids and crinoids appeared. It was long thought that the first true vertebrates (fish — Ostracoderms) appeared in the Ordovician, but recent discoveries in China reveal that they probably originated in the Early Cambrian. [84] The first gnathostome (jawed fish) may have appeared in the Late Ordovician epoch. [85] Chitinozoans, which first appeared late in the Wuliuan, exploded in diversity during the Tremadocian, quickly becoming globally widespread. [86] [87] Several groups of endobiotic symbionts appeared in the Ordovician. [88] [89]

In the Early Ordovician, trilobites were joined by many new types of organisms, including tabulate corals, strophomenid, rhynchonellid, and many new orthid brachiopods, bryozoans, planktonic graptolites and conodonts, and many types of molluscs and echinoderms, including the ophiuroids ("brittle stars") and the first sea stars. Nevertheless, the arthropods remained abundant; all the Late Cambrian orders continued, and were joined by the new group Phacopida. The first evidence of land plants also appeared (see evolutionary history of life).

In the Middle Ordovician, the trilobite-dominated Early Ordovician communities were replaced by generally more mixed ecosystems, in which brachiopods, bryozoans, molluscs, cornulitids, tentaculitids and echinoderms all flourished, tabulate corals diversified and the first rugose corals appeared. The planktonic graptolites remained diverse, with the Diplograptina making their appearance. One of the earliest known armoured agnathan ("ostracoderm") vertebrates, Arandaspis , dates from the Middle Ordovician. [90] During the Middle Ordovician there was a large increase in the intensity and diversity of bioeroding organisms. This is known as the Ordovician Bioerosion Revolution. [91] It is marked by a sudden abundance of hard substrate trace fossils such as Trypanites , Palaeosabella, Petroxestes and Osprioneides . Bioerosion became an important process, particularly in the thick calcitic skeletons of corals, bryozoans and brachiopods, and on the extensive carbonate hardgrounds that appear in abundance at this time.

Flora

Green algae were common in the Late Cambrian (perhaps earlier) and in the Ordovician. Terrestrial plants probably evolved from green algae, first appearing as tiny non-vascular forms resembling liverworts, in the middle to late Ordovician. [93] Fossil spores found in Ordovician sedimentary rock are typical of bryophytes. [94]

Colonization of land would have been limited to shorelines Ordovician Land Scene.jpg
Colonization of land would have been limited to shorelines

Among the first land fungi may have been arbuscular mycorrhiza fungi (Glomerales), playing a crucial role in facilitating the colonization of land by plants through mycorrhizal symbiosis, which makes mineral nutrients available to plant cells; such fossilized fungal hyphae and spores from the Ordovician of Wisconsin have been found with an age of about 460 million years ago, a time when the land flora most likely only consisted of plants similar to non-vascular bryophytes. [95]

Microbiota

Though stromatolites had declined from their peak in the Proterozoic, they continued to exist in localised settings. [96]

End of the period

The Anji Biota (Wenchang Formation, Zhejiang Province, China) preserves abundant and diverse glass sponges and graptolites as well as rare examples of other marine animals (such as the eurypterid Archopterus) living at a depth of several hundred metres. It is dated to just after the Hirnantian mass extinction at the end of the Ordovician period. Anji Biota.jpg
The Anji Biota (Wenchang Formation, Zhejiang Province, China) preserves abundant and diverse glass sponges and graptolites as well as rare examples of other marine animals (such as the eurypterid Archopterus) living at a depth of several hundred metres. It is dated to just after the Hirnantian mass extinction at the end of the Ordovician period.

The Ordovician came to a close in a series of extinction events that, taken together, comprise the second largest of the five major extinction events in Earth's history in terms of percentage of genera that became extinct. The only larger one was the Permian–Triassic extinction event.

The extinctions occurred approximately 447–444 million years ago and mark the boundary between the Ordovician and the following Silurian Period. At that time all complex multicellular organisms lived in the sea, and about 49% of genera of fauna disappeared forever; brachiopods and bryozoans were greatly reduced, along with many trilobite, conodont and graptolite families.

The most commonly accepted theory is that these events were triggered by the onset of cold conditions in the late Katian, followed by an ice age, in the Hirnantian faunal stage, that ended the long, stable greenhouse conditions typical of the Ordovician.

The ice age was possibly not long-lasting. Oxygen isotopes in fossil brachiopods show its duration may have been only 0.5 to 1.5 million years. [98] Other researchers (Page et al.) estimate more temperate conditions did not return until the late Silurian.

The late Ordovician glaciation event was preceded by a fall in atmospheric carbon dioxide (from 7000 ppm to 4400 ppm). [99] [100] The dip may have been caused by a burst of volcanic activity that deposited new silicate rocks, which draw CO2 out of the air as they erode. [100] Another possibility is that bryophytes and lichens, which colonized land in the middle to late Ordovician, may have increased weathering enough to draw down CO2 levels. [93] The drop in CO2 selectively affected the shallow seas where most organisms lived. It has also been suggested that shielding of the sun's rays from the proposed Ordovician ring system, which also caused the Ordovician meteor event, may have also led to the glaciation. [13] As the southern supercontinent Gondwana drifted over the South Pole, ice caps formed on it, which have been detected in Upper Ordovician rock strata of North Africa and then-adjacent northeastern South America, which were south-polar locations at the time.

As glaciers grew, the sea level dropped, and the vast shallow intra-continental Ordovician seas withdrew, which eliminated many ecological niches. When they returned, they carried diminished founder populations that lacked many whole families of organisms. They then withdrew again with the next pulse of glaciation, eliminating biological diversity with each change. [101] Species limited to a single epicontinental sea on a given landmass were severely affected. [40] Tropical lifeforms were hit particularly hard in the first wave of extinction, while cool-water species were hit worst in the second pulse. [40]

Those species able to adapt to the changing conditions survived to fill the ecological niches left by the extinctions. For example, there is evidence the oceans became more deeply oxygenated during the glaciation, allowing unusual benthic organisms (Hirnantian fauna) to colonize the depths. These organisms were cosmopolitan in distribution and present at most latitudes. [102]

At the end of the second event, melting glaciers caused the sea level to rise and stabilise once more. The rebound of life's diversity with the permanent re-flooding of continental shelves at the onset of the Silurian saw increased biodiversity within the surviving Orders. Recovery was characterized by an unusual number of "Lazarus taxa", disappearing during the extinction and reappearing well into the Silurian, which suggests that the taxa survived in small numbers in refugia. [103]

An alternate extinction hypothesis suggested that a ten-second gamma-ray burst could have destroyed the ozone layer and exposed terrestrial and marine surface-dwelling life to deadly ultraviolet radiation and initiated global cooling. [104]

Recent work considering the sequence stratigraphy of the Late Ordovician argues that the mass extinction was a single protracted episode lasting several hundred thousand years, with abrupt changes in water depth and sedimentation rate producing two pulses of last occurrences of species. [105]

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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 445 million years ago (Ma). It is often considered to be the second-largest known extinction event just behind the end-Permian mass extinction, 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.

<span class="mw-page-title-main">Iapetus Ocean</span> Ocean that existed in the late Neoproterozoic and early Paleozoic eras

The Iapetus Ocean existed in the late Neoproterozoic and early Paleozoic eras of the geologic timescale. It was in the southern hemisphere, between the paleocontinents of Laurentia, Baltica and Avalonia. The ocean disappeared with the Acadian, Caledonian and Taconic orogenies, when these three continents joined to form one big landmass called Euramerica. The "southern" Iapetus Ocean has been proposed to have closed with the Famatinian and Taconic orogenies, meaning a collision between Western Gondwana and Laurentia.

<span class="mw-page-title-main">Baltica</span> Late-Proterozoic to early-Palaeozoic continent

Baltica is a paleocontinent that formed in the Paleoproterozoic and now constitutes northwestern Eurasia, or Europe north of the Trans-European Suture Zone and west of the Ural Mountains. The thick core of Baltica, the East European Craton, is more than three billion years old and formed part of the Rodinia supercontinent at c.Ga.

The Hirnantian is the final internationally recognized stage of the Ordovician Period of the Paleozoic Era. It was of short duration, lasting about 2.1 million years, from 445.2 to 443.1 Ma. The early part of the Hirnantian was characterized by cold temperatures, major glaciation, and a severe drop in sea level. In the latter part of the Hirnantian, temperatures rose, the glaciers melted, and sea level returned to the same or to a slightly higher level than it had been prior to the glaciation.

<span class="mw-page-title-main">Tremadocian</span> Lowest stage of Ordovician

The Tremadocian is the lowest stage of Ordovician. Together with the later Floian Stage it forms the Lower Ordovician Epoch. The Tremadocian lasted from 486.85 to 477.1 million years ago. The base of the Tremadocian is defined as the first appearance of the conodont species Iapetognathus fluctivagus at the Global Boundary Stratotype Section and Point (GSSP) section on Newfoundland.

<span class="mw-page-title-main">Cambrian–Ordovician extinction event</span> Mass extinction event about 488 million years ago

The Cambrian–Ordovician extinction event, also known as the Cambrian-Ordovician boundary event, was an extinction event that occurred approximately 485 million years ago (mya) in the Paleozoic era of the early Phanerozoic eon. It was preceded by the less-documented End-Botomian mass extinction around 517 million years ago, and the Dresbachian extinction event about 502 million years ago.

The Hirnantian glaciation, also known as the Andean-Saharan glaciation, Early Paleozoic Ice Age (EPIA), the Early Paleozoic Icehouse, the Late Ordovician glaciation, or the end-Ordovician glaciation, occurred during the Paleozoic from approximately 460 Ma to around 420 Ma, during the Late Ordovician and the Silurian period. The major glaciation during this period was formerly thought only to consist of the Hirnantian glaciation itself but has now been recognized as a longer, more gradual event, which began as early as the Darriwilian, and possibly even the Floian. Evidence of this glaciation can be seen in places such as Arabia, North Africa, South Africa, Brazil, Peru, Bolivia, Chile, Argentina, and Wyoming. More evidence derived from isotopic data is that during the Late Ordovician, tropical ocean temperatures were about 5 °C cooler than present day; this would have been a major factor that aided in the glaciation process.

<span class="mw-page-title-main">Tabulata</span> Order of extinct forms of coral

Tabulata, commonly known as tabulate corals, are an order of extinct forms of coral. They are almost always colonial, forming colonies of individual hexagonal cells known as corallites defined by a skeleton of calcite, similar in appearance to a honeycomb. Adjacent cells are joined by small pores. Their distinguishing feature is their well-developed horizontal internal partitions (tabulae) within each cell, but reduced or absent vertical internal partitions. They are usually smaller than rugose corals, but vary considerably in shape, from flat to conical to spherical.

The Rheic Ocean was an ocean which separated two major paleocontinents, Gondwana and Laurussia (Laurentia-Baltica-Avalonia). One of the principal oceans of the Paleozoic, its sutures today stretch 10,000 km (6,200 mi) from Mexico to Turkey and its closure resulted in the assembly of the supercontinent Pangaea and the formation of the Variscan–Alleghenian–Ouachita orogenies.

The Great Ordovician Biodiversification Event (GOBE) was an evolutionary radiation of animal life throughout the Ordovician period, 40 million years after the Cambrian explosion, whereby the distinctive Cambrian fauna fizzled out to be replaced with a Paleozoic fauna rich in suspension feeder and pelagic animals.

<span class="mw-page-title-main">Laurentia</span> Craton forming the geological core of North America

Laurentia or the North American Craton is a large continental craton that forms the ancient geological core of North America. Many times in its past, Laurentia has been a separate continent, as it is now in the form of North America, although originally it also included the cratonic areas of Greenland and the Hebridean terrane in northwest Scotland. During other times in its past, Laurentia has been part of larger continents and supercontinents and consists of many smaller terranes assembled on a network of early Proterozoic orogenic belts. Small microcontinents and oceanic islands collided with and sutured onto the ever-growing Laurentia, and together formed the stable Precambrian craton seen today.

<span class="mw-page-title-main">Pangaea</span> Supercontinent from the late Paleozoic to early Mesozoic eras

Pangaea or Pangea was a supercontinent that existed during the late Paleozoic and early Mesozoic eras. It assembled from the earlier continental units of Gondwana, Euramerica and Siberia during the Carboniferous approximately 335 million years ago, and began to break apart about 200 million years ago, at the end of the Triassic and beginning of the Jurassic. Pangaea was C-shaped, with the bulk of its mass stretching between Earth's northern and southern polar regions and surrounded by the superocean Panthalassa and the Paleo-Tethys and subsequent Tethys Oceans. Pangaea is the most recent supercontinent to have existed and the first to be reconstructed by geologists.

<span class="mw-page-title-main">Trimerellida</span> Extinct order of brachiopods

Trimerellida is an extinct order of craniate brachiopods, containing the sole superfamily Trimerelloidea and the families Adensuidae, Trimerellidae, and Ussuniidae. Trimerellidae was a widespread family of warm-water brachiopods ranging from the Middle Ordovician to the late Silurian (Ludlow). Adensuidae and Ussuniidae are monogeneric families restricted to the Ordovician of Kazakhstan. Most individuals were free-living, though some clustered into large congregations similar to modern oyster reefs.

<span class="mw-page-title-main">Olev Vinn</span> Estonian paleontologist (born 1971)

Olev Vinn is an Estonian paleobiologist and paleontologist.

The Lundgreni Event, also known as the Mid-Homerian Biotic Crisis, was an extinction event during the middle Homerian age of the Silurian period. Evidence for the event has been observed in Silurian marine deposits in the Iberian Peninsula, Bohemia, and Poland.

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