Petroxestes

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Petroxestes
Petroxestes pera Ordovician Ohio.jpg
Petroxestes pera borings in an Upper Ordovician hardground (Waynesville Formation, southern Ohio).
Trace fossil classification OOjs UI icon edit-ltr.svg
Ichnofamily: Rogerellidae
Ichnogenus: Petroxestes
Wilson & Palmer, 1988
Type ichnospecies
Petroxestes pera
Wilson & Palmer, 1988
Ichnospecies [1]
  • P. alteraJagt et al., 2009
  • P. peraWilson & Palmer, 1988

Petroxestes is a shallow, elongate boring (a type of trace fossil) originally found excavated in carbonate skeletons and hardgrounds of the Upper Ordovician of North America. [2] [3] These Ordovician borings were likely made by the mytilacean bivalve Corallidomus as it ground a shallow groove in the substrate to maintain its feeding position. [4] They are thus the earliest known bivalve borings. [5] Petroxestes was later described from the Lower Silurian of Anticosti Island (Canada). [6] and the Miocene of the Caribbean. [7]

Related Research Articles

<span class="mw-page-title-main">Ordovician</span> Second period of the Paleozoic Era 485–444 million years ago

The Ordovician is a geologic period and system, the second of six periods of the Paleozoic Era. The Ordovician spans 41.6 million years from the end of the Cambrian Period 485.4 Ma to the start of the Silurian Period 443.8 Ma.

<span class="mw-page-title-main">Silurian</span> Third period of the Paleozoic Era, 443–419 million years ago

The Silurian is a geologic period and system spanning 24.6 million years from the end of the Ordovician Period, at 443.8 million years ago (Mya), to the beginning of the Devonian Period, 419.2 Mya. The Silurian is the shortest period of the Paleozoic Era. As with other geologic periods, the rock beds that define the period's start and end are well identified, but the exact dates are uncertain by a few million years. The base of the Silurian is set at a series of major Ordovician–Silurian extinction events when up to 60% of marine genera were wiped out.

<span class="mw-page-title-main">Trace fossil</span> Geological record of biological activity

A trace fossil, also known as an ichnofossil, is a fossil record of biological activity by lifeforms but not the preserved remains of the organism itself. Trace fossils contrast with body fossils, which are the fossilized remains of parts of organisms' bodies, usually altered by later chemical activity or mineralization. The study of such trace fossils is ichnology and is the work of ichnologists.

<span class="mw-page-title-main">Bioerosion</span> Erosion of hard substrates by living organisms

Bioerosion describes the breakdown of hard ocean substrates – and less often terrestrial substrates – by living organisms. Marine bioerosion can be caused by mollusks, polychaete worms, phoronids, sponges, crustaceans, echinoids, and fish; it can occur on coastlines, on coral reefs, and on ships; its mechanisms include biotic boring, drilling, rasping, and scraping. On dry land, bioerosion is typically performed by pioneer plants or plant-like organisms such as lichen, and mostly chemical or mechanical in nature.

Cryptospores are microscopic fossilized spores produced by embryophytes. They first appear in the fossil record during the middle of the Ordovician period, as the oldest fossil evidence for the colonization of land by plants. A similar category is miospores, a term generally used for spores smaller than 200 μm. Both cryptospores and miospores are types of palynomorphs.

<span class="mw-page-title-main">Evolution of molluscs</span> The origin and diversification of molluscs through geologic time

The evolution of the molluscs is the way in which the Mollusca, one of the largest groups of invertebrate animals, evolved. This phylum includes gastropods, bivalves, scaphopods, cephalopods, and several other groups. The fossil record of mollusks is relatively complete, and they are well represented in most fossil-bearing marine strata. Very early organisms which have dubiously been compared to molluscs include Kimberella and Odontogriphus.

Praenuculidae is an extinct family of prehistoric bivalves in the superfamily Nuculoidea. Praenuculidae species lived from the early Ordovician, Arenig stage through the Early Devonian Emsian stage. Praenuculidae fossils are found worldwide, present on every continent except Antarctica. Species in this family are thought to have been sessile, attached to the substrate in shallow infaunal marine water environments, where they formed shells of an aragonite composition. The family Praenuculidae was named by A. Lee McAlester in 1969.

<span class="mw-page-title-main">Calcite sea</span> Sea chemistry favouring low-magnesium calcite as the inorganic calcium carbonate precipitate

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<span class="mw-page-title-main">Carbonate hardgrounds</span>

Carbonate hardgrounds are surfaces of synsedimentarily cemented carbonate layers that have been exposed on the seafloor. A hardground is essentially, then, a lithified seafloor. Ancient hardgrounds are found in limestone sequences and distinguished from later-lithified sediments by evidence of exposure to normal marine waters. This evidence can consist of encrusting marine organisms, borings of organisms produced through bioerosion, early marine calcite cements, or extensive surfaces mineralized by iron oxides or calcium phosphates. Modern hardgrounds are usually detected by sounding in shallow water or through remote sensing techniques like side-scan sonar.

<span class="mw-page-title-main">Evolution of fungi</span> Origin and diversification of fungi through geologic time

Fungi diverged from other life around 1.5 billion years ago, with the glomaleans branching from the "higher fungi" (dikaryans) at ~570 million years ago, according to DNA analysis. Fungi probably colonized the land during the Cambrian, over 500 million years ago,, and possibly 635 million years ago during the Ediacaran, but terrestrial fossils only become uncontroversial and common during the Devonian, 400 million years ago.

<i>Trypanites</i> Trace fossil

Trypanites is a narrow, cylindrical, unbranched boring which is one of the most common trace fossils in hard substrates such as rocks, carbonate hardgrounds and shells. It appears first in the Lower Cambrian, was very prominent in the Ordovician Bioerosion Revolution, and is still commonly formed today. Trypanites is almost always found in calcareous substrates, most likely because the excavating organism used an acid or other chemical agent to dissolve the calcium carbonate. Trypanites is common in the Ordovician and Silurian hardgrounds of Baltica.

<i>Gastrochaenolites</i> Trace fossil

Gastrochaenolites is a trace fossil formed as a clavate (club-shaped) boring in a hard substrate such as a shell, rock or carbonate hardground. The aperture of the boring is narrower than the main chamber and may be circular, oval, or dumb-bell shaped. Gastrochaenolites is most commonly attributed to bioeroding bivalves such as Lithophaga and Gastrochaena. The fossil ranges from the Ordovician to the Recent. The first Lower Jurassic Gastrochaenolites ichnospecies is Gastrochaenolites messisbugi Bassi, Posenato, Nebelsick, 2017. This is the first record of boreholes and their producers in one of the larger bivalves of the globally occurring Lithiotis fauna which is a unique facies in the Lower Jurassic Tethys and Panthalassa.

<i>Rogerella</i> Trace fossil

Rogerella is a small pouch-shaped boring with a slit-like aperture currently produced by acrothoracican barnacles. These crustaceans extrude their legs upwards through the opening for filter-feeding. They are known in the fossil record as borings in carbonate substrates from the Devonian to the Recent.

<i>Entobia</i> Trace fossil

Entobia is a trace fossil in a hard substrate formed by sponges as a branching network of galleries, often with regular enlargements termed chambers. Apertural canals connect the outer surface of the substrate to the chambers and galleries so the sponge can channel water through its tissues for filter feeding. The fossil ranges from the Devonian to the Recent.

The Claerwen Fault is a major SW-NE trending fault in central Wales. It was active as a normal fault during deposition of Late Ordovician to mid-Silurian sedimentary rocks, downthrowing to the northwest. The estimated throw on the fault increases from about 100 m at a shallow level to about 1000 m at depth. There is no discernible change in the grade of metamorphism associated with the Caledonian Orogeny across the fault, suggesting that it was not reactivated later.

<i>Helminthopsis</i> Trace fossil

Helminthopsis is the ichnogenus of a type of trace fossil that is found preserved on the bedding planes of fine-grained sedimentary rocks. It is characterized by short, curvilinear, non-branching, parallel-sided, unlined traces on bedding surfaces. It is thought to represent the submarine feeding trails of an invertebrate organism that worked the surface of muddy substrates in search of food. Because Helminthopsis traces never cross over themselves, the ichnogenus is distinguished from similar traces assigned to the Gordia ichnogenus. The similar sounding, but now obsolete, ichnogenus Helminthoida refers to a somewhat similar trace characterized by regular, back-and-forth meanders, whereas Helminthopsis traces are irregular.

<i>Osprioneides</i> Trace fossil

Osprioneides is an ichnogenus of unbranched, elongate borings in lithic substrate with oval cross−section, single−entrance and straight, curved or irregular course. Osprioneides kampto Beuck and Wisshak, 2008 is the largest known Palaeozoic boring trace. It occurs in the Ordovician and Silurian (Wenlock) of Baltica. The borings are up to 120 mm long measuring 5–17 mm in diameter. The distribution of Osprioneides is more environmentally limited than that of Trypanites in the Silurian of Saaremaa, Estonia (Baltica). Osprioneides probably occurred only in large hard substrates of relatively deepwater muddy bottom open shelf environments. Osprioneides were relatively rare, as compared to Trypanites-Palaeosabella borings in the Wenlock of Saaremaa.

The Jupiter Formation is a geologic formation in Quebec, well-exposed in the southern third of Anticosti Island and lying in the St Lawrence River Valley. It preserves fossils dating back to the Silurian period.

<span class="mw-page-title-main">Bioclaustration</span>

Bioclaustration is kind of interaction when one organism is embedded in a living substrate ; it means "biologically walled-up". In case of symbiosis the walling-up is not complete and both organisms stay alive.

<span class="mw-page-title-main">Geology of Hainan Island</span>

Hainan Island, located in the South China Sea off the Chinese coast and separated from mainland China by the Qiongzhou Strait, has a complex geological history that it has experienced multiple stages of metamorphism, volcanic and intrusive activities, tectonic drifting and more. The oldest rocks, the Proterozoic metamorphic basement, are not widely exposed, but mostly found in the western part of the Island.

References

  1. Wisshak, M.; Knaust, D.; Bertling, M. (2019). "Bioerosion ichnotaxa: review and annotated list". Facies. 65 (2): 24. doi:10.1007/s10347-019-0561-8.
  2. Wilson, M.A., Palmer, T.J. (1988). "Nomenclature of a bivalve boring from the Upper Ordovician of the midwestern United States". Journal of Paleontology. 62 (2): 306–308. doi:10.1017/S0022336000029978. S2CID   131394939.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. Wilson, M.A., Palmer, T.J. (2006). "Patterns and processes in the Ordovician Bioerosion Revolution". Ichnos. 13 (3): 109–112. doi:10.1080/10420940600850505. S2CID   128831144.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. Pojeta, J., Jr., Palmer, T.J. (1976). "The origin of rock boring in mytilacean pelecypods". Alcheringa. 1 (2): 167–179. doi:10.1080/03115517608619068.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. Taylor, P.D., Wilson. M.A. (2003). "Palaeoecology and evolution of marine hard substrate communities". Earth-Science Reviews. 62 (1–2): 1–103. Bibcode:2003ESRv...62....1T. doi:10.1016/S0012-8252(02)00131-9.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. Tapanila, L., Copper, P. (2002). "Endolithic trace fossils in Ordovician-Silurian corals and stromatoporoids, Anticosti Island, eastern Canada". Acta Geológica Hispánica. 37: 15–20.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  7. Pickerill, R.D., Donovan, S.K., Portell, R.W. (2001). "The bioerosional ichnofossil Petroxestes pera Wilson and Palmer from the Middle Miocene of Carriacou, Lesser Antilles". Caribbean Journal of Science. 37: 130–131.{{cite journal}}: CS1 maint: multiple names: authors list (link)