Saltrio Formation | |
---|---|
Stratigraphic range: Early Sinemurian ~ | |
Type | Geological formation |
Unit of | Calcari Selciferi Lombardi Unit |
Underlies | Moltrasio Formation |
Overlies | Tremona Formation |
Lithology | |
Primary | Limestone |
Location | |
Coordinates | 45°54′N8°54′E / 45.9°N 8.9°E |
Approximate paleocoordinates | 33°06′N14°48′E / 33.1°N 14.8°E |
Region | Lombardy |
Country | Italy |
Type section | |
Named for | Saltrio |
Named by | Antonio Stoppani [1] |
The Saltrio Formation is a geological formation in Italy. It dates back to the Early Sinemurian, and would have represented a pelagic or near-epicontinental environment, judging by the presence of marine fauna such as the nautiloid Cenoceras . [2] [3] The Fossils of the Formation were described on the late 1880s and revised on 1960s, finding first marine biota, such as Crinoids, Bivalves and other fauna related to Epicontinental basin deposits. [4]
The main outcrop of the formation, represents an active private extraction site. The first extraction activities of the famous Saltrio stone give back to the times of the ancient Romans, with modern reports of activity in this quarry since 1400. [5] In the Monte Oro area, on the southern slope of Monte Orsa, there were numerous trench quarries which were used to extract this precious rock, used both for structural constructions and for the production of artefacts and artistic works. In more recent times the mining activity has been transformed and we have moved from the extraction of stone for construction to the extraction for the production of stabilized and split crushed stone, useful for the production of motorway foundations and mixtures for the production of asphalt. To date it is the only active quarry where Saltrio stone is extracted. [5]
In today's quarry what is mainly known as the Saltrio Formation emerges, i.e., a group of stratified rocks dating back to the Lower Jurassic. The stratigraphy, however, is much more complex, even if so far no study has focused on this topic. Inside the quarry, Dolomia principale sediment emerges dating back to the Upper Triassic (Norian); yet the succession is dominated by the Saltrio Formation, here 15-20 meters thick. [6]
Above, the Moltrasio Formation emerges, a greyish-brown limestone composed of biocalcarenite and containing widespread nodules of spongolitic silica. This rock is rarely fossiliferous except in the contact areas between the Formations. At the roof of the Moltrasio Fm, a whitish yellow limestone emerges, again of marine-pelagic origin, where there is a lot of micro-diffused silica within the sediment. [6]
Since the early 1900s, fossil finds have been known in the Salnova Quarry and in the various quarry sites present in the surroundings of this site. The first written testimonies, and subsequent revisions, are reported starting from the sixties by Giulia Sacchi Vialli. The scholar describes the fossil faunas of Saltrio by listing and detailing various taxa belonging to ammonoids, nautiloids, gastropods, crinoids, brachiopods and bivalves. [4]
In that period, the great phase of extraction of ornamental stone using manual-mechanical methods had just ended in the quarry. Paleontologists could only recover fossils from the waste flakes near the quarry and therefore the possibility of seeing more specimens was limited to the length of manual operations. In those years, however, the quarry was acquired by Salnova SPA (1969): the purpose of the extracted material, and therefore the extraction method and processing, changed. From classic and manual extraction we move on to the use of heavy mechanical means and extraction with explosives: the moved rubble increases considerably, making it easier to observe other specimens, new lithologies and above all different faunas. [5]
The fauna present at the base of the Saltrio Formation is condensed and includes ammonoids of species attributed to the entire Upper Sinemurian. The taxa attributable to the Lower Sinemurian found in the Saltrio quarries probably come from the base of the formation or have been reworked. [4] According to Sacchi-Vialli, the Formation includes taxa indicative of all the biozones between the Bucklandi Zone (Lower Sinemurian) and the Obtusum Zone, and possibly also of the Oxynotum Zone of the Upper Sinemurian, present at the base of the Formation. [4] The contact between the Main Dolomite and the Saltrio Formation also contains selachian teeth, glauconite and phosphated internal models of ammonites. [7]
Since the beginning of the jurassic, from Hettangian to earliest Sinemurian on the western Lombardy Basin there was a notorious continental area that was found to be wider than previously thought, where a warm humid paleoclimate developed. [8] The basin facies are characterized by a gradual transition from Upper Rhaetian shallow-water carbonates to Lombard siliceous limestone and thick Lower Liassic series. [9] The Dinosaur Fossils found on the Saltrio formation can have been translated from this area, or alternatively, the Arbostora swell (that was located at the north of the Saltrio formation, on Switzerland). [9] This was an emerged structural high close to the Saltrio Formation, that caused a division between two near subsiding basins located at Mt. Nudo (East) and Mt. Generoso (West). [9] It settled over a carbonate platform linked with other wider areas that appear along the west to the southeast, developing a large shallow water gulf to the north, where the strata deposited was controlled by a horst and tectonic gaben. [9]
The Saltrio layers represent a unique sedimentary environment that is different from both the "Formazione di Saltrio" and the "Saltrio calcarenite" described by earlier researchers. These layers are characterized by being transgressive deposits, meaning they formed as the sea advanced over previously exposed land. The Saltrio deposits show signs of stratigraphic condensation, which refers to slow sediment accumulation over time, often resulting in hardgrounds, surfaces drilled by marine organisms, and the presence of minerals like Glauconite and Phosphorite. [9] Biologically, these layers are rich in fossils, especially Encrinite (crinoid-rich limestones) and bivalve lumachellas (fossilized bivalve shells). Other marine creatures like cephalopods and brachiopods appear occasionally. Faunas from the condensed Saltrio beds indicate early subsidence in the Hettangian. Additionally, the involutine limestones with a rich ammonite fauna support subsidence during the same period. The sediment composition varies in different areas, often containing reworked material from older rocks. [9] The Saltrio environment was complex, with different layers showing distinct conditions. In some areas, the Saltrio layers blend with the "Broccatello d'Arzo", a related limestone formation, but they can still be separated based on differences in their structure and fossil content. The region also experienced sedimentary discontinuities, where layers were not deposited continuously, likely due to tectonic activity or submarine erosion. [9] Overall, the Saltrio paleoenvironment reflects a shallow marine setting with fluctuating sea levels, rich marine life, and periods of sediment reworking and erosion, all influenced by local tectonics. [9]
Several outcrops of the so-called “terra rossa” paleosoils were also found, including at Castello Cabiaglio-Orino, a dozen of kilometers West of Saltrio. [10] [11] This outcrops show that the emerged areas that on the Hettangian-Sinemurian, the current location of the modern Maggiore Lake were covered with forests, what was proven by the presence of large plant fragments on the Moltrasio Formation. [8] The plants have been recovered between the locations of Cellina and Arolo (eastern side of Lake Maggiore), from rocks that have been found to be coeval in age to the Saltrio Formation. [12] The Flora includes genera such as Bennettitales ( Ptilophyllum ), terrestrial Araucariaceae ( Pagiophyllum ), and Cheirolepidiaceae ( Brachyphyllum ), that developed on inland areas with dry-warm conditions. [12]
The ammonites from the Saltrio Formation allow the formation to be dated to the Early Sinemurian. Animals probably lived in emerged parts of carbonated platform or an area to the northwest, whose presence had never been established. In the early Sinemurian, the Arbostora swell became again a shallow open sea (ramp-slope), still surrounded South and South-West by emerged land. The dinosaur bones where washed on this period, flowed into a gulf of the Mt. Nudo basin, where they became fossilized. The latter possibility was suggested by Lualdi (1999), in which he analyzed the local geology based on the presence of terrestrial plants and terrigenous content (sands from igneous or metamorphic rocks exposed to sub-aerial erosion) in the limestones. [12] Terrestrial plants are essentially represented by leaves and small branches of Araucariaceans and Bennettitales, the typical flora of the early Mesozoic. However, plants and sand (which are not abundantly referred) can be carried by wind and ocean currents. Also, according to the most current paleogeographic maps, truly continental land located closer these Jurassic times lower were the Mountains of Sardinia, Corsica, distanced many tens of kilometers WNW. [13] Coeval and slightly younger in age, large dinosaurs, carnivorous and herbivorous, were present as shown in various footprints of the lower Jurassic (Hettangian-Sinemurian) in the province of Trento, around 160 kilometres (99 mi) east of Saltrio, which changed the traditional view of the palaeoenvironments and paleogeography of the region, considered a tropical sea with small islands of the atoll type. [14] Fossil footprints and tracks are preserved in tidal carbonates deposited in a relatively narrow carbonated platform in Trento, flanked to the east and west by relatively deep marine basins. Large theropods could not live in an atoll, since large areas had to be emersed to provide food and fresh water, and their herbivorous prey needed land with vegetation. [15]
"It is more likely that the Peri-Adriatic Platforms worked with temporary continental bridges that connected with Laurasia Gondwana in central Tethis, allowing migration between the two hemispheres and colonization of local coastal habitats. During the marine transgressions, some of these lands were isolated, implicating genetic Mutations in their terrestrial faunas, with typical biological consequences, as endemism and possible dwarfism". [16]
Rhynchonellata | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
C. variabilis |
| “Salnova” quarry | A Rhynchonellatan, member of the family Wellerellidae inside Rhynchonellida. Identified originally as "Rhynchonella variabilis". | ||
L. rostrata |
| “Salnova” quarry | A Rhynchonellatan, member of the family Spiriferinidae inside Spiriferinida. Was identified originally as "Spiriferina haasi". | ||
L. punctata |
| “Salnova” quarry | A Rhynchonellatan, member of the family Lobothyrididae inside Terebratulida. Was identified originally as "Terebratula punctata". | ||
S. expansa |
| “Salnova” quarry | A Rhynchonellatan, type member of the family Spiriferinidae inside Spiriferinida. It is a rather a complex series of specimens, whose classification is controversial. | ||
R. acanthica |
| “Salnova” quarry | A Rhynchonellatan, member of the family Wellerellidae inside Rhynchonellida. Another series of Specimens of uncertain placement. | ||
Bivalvia | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
|
| “Salnova” quarry | A Clam, type member of the family Astartidae inside Carditida. Some shells identified as Cardium probably belong to this genus. | ||
|
| “Salnova” quarry | A Pearl Oyster, member of the family Pteriidae inside Ostreida. Abundant and rather easy to identify. | ||
|
| “Salnova” quarry | A Scallop, member of the family Pectinoidae inside Pectinida. It was identified originally as "Pecten (Pseudamusium) hehlii". | ||
|
| “Salnova” quarry | A Clam, type member of the family Cardiniidae inside Carditida. Epicontinental deposits genus, rather abundant locally. Cardinia rugosa was first discovered on this formation. | ||
|
| “Salnova” quarry | A Clam, member of the family Cardiniidae inside Carditida. Rare locally, with some specimens considered dubious. | ||
|
| “Salnova” quarry | A Scallop, member of the family Pectinoidae inside Pectinida. It was identified as "Pecten (Chlamys) textorius". | ||
|
| “Salnova” quarry | A Clam, member of the family Lucinidae inside Lucinida. Was first identified on the Formation. | ||
|
| “Salnova” quarry | A Clam, member of the family Lucinidae inside Lucinida. First identified on the formation. | ||
|
| “Salnova” quarry | An Oyster, type member of the family Gryphaeidae inside Ostreida. Related with specimens of the Blue Lias Formation. | ||
|
| “Salnova” quarry | A File Clam, member of the family Limidae inside Pectinida. Included on the Genus Plagiostoma, the status of the species is rather dubious. | ||
|
| “Salnova” quarry | A Clam, type member of the family Lucinidae inside Lucinida. Uncertain classification due to be based on fragmentary shell remains. | ||
|
| “Salnova” quarry | A Mussel, member of the family Mytilidae inside Mytilida. Identified as the genus "Modiola", now junior synonym of Modiolus. | ||
|
| “Salnova” quarry | A Clam, member of the family Pleuromyidae inside Pholadida. Rather rare and controversial genus. | ||
|
| “Salnova” quarry | An Oyster, type member of the family Ostreidae inside Ostreida. Rather Abundant genus, but lacks specimens enough complete for a formal identification. | ||
|
| “Salnova” quarry | A Scallop, type member of the family Pectinoidae inside Pectinida. Mistake for other related genera on the deposit, it is among the most abundant local Scallops, although the affinities with the genus Pecten haven't been proved. | ||
|
| “Salnova” quarry | A Clam, type member of the family Pholadomyidae inside Pholadomyida. Mostly incomplete specimens, what makes nearly impossible to assigante a concrete species. | ||
|
| “Salnova” quarry | A File Clam, member of the family Limidae inside Pectinida. Identified originally as "Lima (Plagiostoma) gigantea". | ||
|
| “Salnova” quarry | A Clam, type member of the family Pleuromyidae inside Pholadida. Present on most of the deposits of the formation, with P. saltriensis being first discovered on the location. | ||
|
| “Salnova” quarry | A Clam, member of the family Lucinidae inside Lucinida. Identified originally as "Fimbria (Sphaeriola) sp.". | ||
|
| “Salnova” quarry | A Clam, member of the family Prospondylidea inside Pterioida. Is based on a few specimens | ||
Gastropoda | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
|
|
| A Sea Snail, type member of the family Pleurotomariidae inside Pleurotomarioidea. Relatively abundant genus, found specially on deposits with terrestrial debris input. | ||
|
|
| A Sea Snail, type member of the family Trochidae inside Trochoidea. Rather common, found associated with Echinoderm debris. | ||
Cephalopoda | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
|
|
| An Ammonitidan, member of the family Arietitidae inside Psiloceratoidea. | ||
|
|
| An Ammonitidan, type member of the family Arietitidae inside Psiloceratoidea. The main Ammonite identified locally. | ||
|
|
| A Nautilidan, type member of the family Cenoceratidae inside Nautilidae. The most abundant local cefalophod, Cenoceras was identified as member of the genus Nutilus originally. | ||
|
|
| An Ammonitidan, member of the family Arietitidae inside Psiloceratoidea. One of the main ammonites identified along the local dinosaur remains. | ||
|
|
| An Ammonitidan, type member of the family Oxynoticeratidae inside Ammonitida. Not the most abundant, but rather common. | ||
Echinodermata | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
| Multiple ossicles | M. Campo dei Fiori | An Crinoidean, member of the family Isocrininae inside Isocrinida. | ||
| Multiple ossicles | “Salnova” quarry | An Echinoidean, type member of the family Miocidaridae inside Cidaroida. Related to epicontinental to pelagic waters. | ||
| Multiple ossicles | “Salnova” quarry | A Sea lily, type member of the family Millericrinida inside Crinoidea.The main Crinoid identified locally. | ||
|
| Mount Campo dei Fiori | An Ophiuridan, member of the family Ophiodermatidae inside Ophiodermatina. Extant tropical species like Ophioderma are benthic predators and scavengers that show the same short spines seen in Palaeocoma. [24] | ||
|
| “Salnova” quarry | A Sea lily, type member of the family Pentacrinitidae inside Isocrinida. A Pelagic crinoid that live attached to washed wood. | ||
In 2016 new vertebrate remains were discovered in the Salnova quarry, the remains are being studied to understand if it is a new dinosaur or some other creature. [25] [26] Latter has been confirmed to be Marine Diapsid material. [27]
Osteichthyes | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
Notidanoides [7] |
|
| “Salnova” quarry | A Crassodontidanidae Hexanchiform | |
Indeterminate |
| “Salnova” quarry | Outside Saltriovenator, initially, few vertebrate remains were found associated to this bone assemblage, except for one tooth and one jaw fragment pertaining to a bony fish. [3] | ||
Sphenodus [7] |
|
| “Salnova” quarry | An Orthacodontidae Synechodontiform | |
Ichthyosaurians | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
|
| “Salnova” quarry | A Neoichthyosaurian of the family Ichthyosauridae. | ||
|
| “Salnova” quarry | A Neoichthyosaurian of the family Temnodontosauridae. Quoted on the 1880s, specimen that apparently has never been described or figured and whose present repository is unknown | ||
Pterosaurs | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
"Pterodactylus" longirostris |
| “Salnova” quarry | A Pterosaur. Quoted on the 1880s, specimen that apparently has never been fully described or figured and whose present repository is unknown | ||
Theropods | |||||
---|---|---|---|---|---|
Genus | Species | Material | Location | Notes | Images |
| “Salnova” quarry. [13] | The oldest known Ceratosaur, falling outside Neoceratosauria, being sister taxa to the maroccan genus Berberosaurus . Saltriovenator is also the largest known Theropod of the Lower Jurassic. It probably was washed into the Sea. [3] Traces on the bones show that the dinosaur carcass remained exposed to the water-sediment interface for months or years, long enough to first be defleshed by mobile scavengers, then colonized by a microbial community that spanned the bone–water interface, which in turn attracted slow-moving grazers and epibionts. [3] | |||
Anina is a town in the Banat region of Romania, in Caraș-Severin County, with a population of 5,521 in 2021. The town administers one village, Steierdorf.
The Early Jurassic Epoch is the earliest of three epochs of the Jurassic Period. The Early Jurassic starts immediately after the Triassic–Jurassic extinction event, 201.3 Ma, and ends at the start of the Middle Jurassic 174.7 ±0.8 Ma.
Saltriovenator is a genus of ceratosaurian dinosaur that lived during the Sinemurian stage of the Early Jurassic in what is now Italy. The type and only species is Saltriovenator zanellai; in the past, the species had been known under the informal name "saltriosaur". Although a full skeleton has not yet been discovered, Saltriovenator is thought to have been a large, bipedal carnivore similar to Ceratosaurus.
The Hettangian is the earliest age and lowest stage of the Jurassic Period of the geologic timescale. It spans the time between 201.3 ± 0.2 Ma and 199.3 ± 0.3 Ma. The Hettangian follows the Rhaetian and is followed by the Sinemurian.
Sarcosaurus is a genus of basal neotheropod dinosaur, roughly 3.5 metres (11 ft) long. It lived in what is now England and maybe Ireland and Scotland during the Hettangian-Sinemurian stages of the Early Jurassic, about 199-196 million years ago. Sarcosaurus is one of the earliest known Jurassic theropods, and one of only a handful of theropod genera from this time period. Along with Dracoraptor hanigani it is one of the two described neotheropods from the lowermost Jurassic of the United Kingdom.
Dapedium is an extinct genus of primitive marine neopterygian ray-finned fish. The first-described finding was an example of D. politum, found in the Lower Lias of Lyme Regis, on the Jurassic Coast of England. Dapedium lived in the Late Triassic to the Middle Jurassic period, from the late Norian to the early Aalenian.
The Ziliujing Formation is a geological formation in China, It is Early Jurassic in age. It is part of the stratigraphy of the Sichuan Basin. The dinosaur Gongxianosaurus and indeterminate theropod material are known from the Dongyuemiao Member of the formation, as well as dinosaur footprints, Zizhongosaurus and indeterminate prosauropods from the Da'anzhai Member. The basal sauropod Sanpasaurus is known from the Maanshan Member. The basal ornithschian Archaeocursor is known from the formation. An possible unnamed stegosaur and the pliosauroid plesiosaur Sinopliosaurus are also known from this formation but they were found an indeterminate member. An unnamed teleosaurid known from a complete skull has also been found in the formation, pending a formal description. The deposition environment during the Da'anzhai Member in the lower Toarcian is thought to have been that of a giant freshwater lake encompassing the whole of the Sichuan basin, around 3 times larger than Lake Superior, coeval with the Toarcian Oceanic Anoxic Event around 183 Ma. The Sinemurian-Pliensbachian boundary event has been recorded on the top of the Dongyuemiao Member, while lower parts of this member are of Earliest Sinemurian age.
Monte San Giorgio is a Swiss mountain and UNESCO World Heritage Site near the border between Switzerland and Italy. It is part of the Lugano Prealps, overlooking Lake Lugano in the Swiss Canton of Ticino.
The Blue Lias is a geological formation in southern, eastern and western England and parts of South Wales, part of the Lias Group. The Blue Lias consists of a sequence of limestone and shale layers, laid down in latest Triassic and early Jurassic times, between 195 and 200 million years ago. The Blue Lias is famous for its fossils, especially ammonites.
The Kota Formation is a geological formation in India. The age of the Kota Formation is uncertain; it is commonly considered to date to the Early Jurassic, but some studies have suggested it may extend into the Middle Jurassic or even later. It conformably overlies the Lower Jurassic Upper Dharmaram Formation and is unconformably overlain by the Lower Cretaceous Gangapur Formation. It is split into a Lower Member and Upper Member. The Lower Member is approximately 100 m thick while the Upper Member is 490 m thick. Both subunits primarily consist of mudstone and sandstone, but near the base of the upper unit there is a 20-30 metre thick succession of limestone deposited in a freshwater setting.
The Höganäs Formation is a Late Triassic to Early Jurassic geologic formation in Skåne, Sweden. The formation is mostly known for its incredible flora collection from the Bjuv member, composed of over 110 species, and also includes several vertebrate remains, such as fishes, amphibians and dinosaur tracks & remains, although none have yet been referred to a specific genus. It´s regional equivalent is the Zagaje Formation in Poland.
Stegomosuchus is an extinct genus of small protosuchian crocodyliform. It is known from a single incomplete specimen discovered in the late 19th century in Lower Jurassic rocks of south-central Massachusetts, United States. It was originally thought to be a species of Stegomus, an aetosaur, but was eventually shown to be related to Protosuchus and thus closer to the ancestry of crocodilians. Stegomosuchus is also regarded as a candidate for the maker of at least some of the tracks named Batrachopus in the Connecticut River Valley.
The Zagaje Formation is a Latest Triassic-Early Jurassic Epoch (Rhaetian-Sinemurian) geologic formation located mostly in Poland with layers also exposed in north Germany. This unit is known for its diverse Ichnofossil assemblages, with traces of invertebrates along vertebrate footprints, as well plants, large coal accumulations, invertebrate remains and ichnofossils. The Zagaje Formation correlates with The lower part of the Höganäs Formation in Scania, as well the Munkerup Member and the Gassum Formation in Denmark.
The Hasle Formation is a geologic formation on the island on Bornholm, Denmark. It is of early to late Pliensbachian age. Vertebrate fossils have been uncovered from this formation. The type section of the formation is found at the south of the costal Hasle Town, and it is composed by rusty yellow to brownish siltstones and very fine-grained sandstones. The southernmost arch, Hvjdoddebuen, is not as fossil-bearing as the type unit in Hasle. The formation can be separated in two different petrographic types: type 1 sandstones are friable with layers and lenses of concretionary siderite and type 2 well-cemented sandstones. Both types where deposited in a relatively high-energy marine environment with a diagenetic pattern that demonstrates a close relation to various phases of subsidence and uplift in the tectonically unstable Fennoscandian Border Zone. Most of its deposition happened on a storm-dominated shoreface, with the exposed parts deposited in an open marine shelf within 1–2 km distance from the fault-controlled coastlines. However, recent works have recovered terrestrial fauna from it, including a footprint, suggesting easterly winds and low tide could have exposed the inner parts of the upper shoreface, and create long-lasting Floodplain-type environments. Field works since 1984 have shown a mostly hummocky cross-stratified deposition, with great complexity of the sediments that suggests very complicated and variable flow conditions, with Megaripples derived from storm events. Storms were frequent and the coastline faced a wide epeiric sea with a fetch towards the west of possibly 1000 kilometers. The Jamesoni–Ibex Chronozone in the Central European Basin represents a clear sea Transgression, due to the appearance of ammonites from Thuringia and southern Lower Saxony, showing a full marine ingression towards the west. This rise in the sea level is also measured in the north, as is proven by the presence of Uptonia jamesoni in Kurremölla and Beaniceras centaurus plus Phricodoceras taylori on the Hasle Formation. The whole Hasle Sandstones are a result of this rise in the sea level, where the marine sediments cover the deltaic layers of the Rønne Formation. The rise in the sea level is observed on palynology, as on the Hasle Formation Nannoceratopsis senex (Dinoflajellate) and Mendicodinium reticulaturn appear, indicating a transition from paralic and restricted marine to fully marine.
The Charmouth Mudstone Formation is a geological formation in England, dating to the Early Jurassic (Sinemurian–Pliensbachian). It forms part of the lower Lias Group. It is most prominently exposed at its type locality in cliff section between Lyme Regis and Charmouth but onshore it extends northwards to Market Weighton, Yorkshire, and in the subsurface of the East Midlands Shelf and Wessex Basin. The formation is notable for its fossils, including those of ammonites and marine reptiles and rare dinosaur remains. The formation played a prominent role in the history of early paleontology, with its Lyme Regis-Charmouth exposure being frequented by fossil collectors including Mary Anning.
The Drzewica Formation is a geologic formation in Szydłowiec, Poland. It is Pliensbachian in age. Vertebrate fossils have been uncovered from this formation, including dinosaur tracks. The Drzewica Formation is part of the Depositional sequence IV-VII of the late lower Jurassic Polish Basin, with the IV showing the presence of local Alluvial deposits, with possible meandriform deposition origin, dominated in Jagodne and Szydłowiec, while delta system occurred through the zone of the modern Budki. The sequence V shows a reduction of the erosion in the Zychorzyn borehole of the Drzewica Formation, showing changes on the extension of the marine facies, where upper deposits change from Alluvial to Deltaic-Seashore depositional settings. VI-VII facies were recovered on the Brody-Lubienia borehole, with a lower part exposed on the village of Śmiłów that shows a small fall of the Sea level. The stathigraphic setting of the dinosaur tracks reported from the formation suggest a Seashore or Deltaic barrier. Body fossils reported include bivalves, palynology, fossil trunks, roots. Trunks of coniferous wood, especially Cheirolepidiaceae and Araucariaceae trees show the occurrence of vast coniferous forests around the tracksite. The association of forests and dinosaur megafauna on the Pliensbachian suggests also a colder and specially dry ecosystem. Drzewica deposits where in part to be a gigantic shore barrel, setting at the time where the Polish basin sea was at its lowest point. Other related units are Fjerritslev or Gassum Formation, Hasle & Sorthat Formation (Bornholm), upper Neringa Formation (Lithuania) and abandoned informal units in other regions of Poland: upper Sawêcin beds, Wieluñ series or Bronów series.
The Rotzo Formation is a geological formation in Italy, dating to roughly between 192 and 186 million years ago and covering the Pliensbachian stage of the Jurassic Period in the Mesozoic Era. Has been traditionally classified as a Sinemurian-Pliensbachian Formation, but a large and detailed dataset of isotopic 13C and 87Sr/86Sr data, estimated the Rotzo Formation to span only over the Early Pliensbachian, bracketed between the Jamesoni-Davoei biozones, marked in the Loppio Oolitic Limestone–Rotzo Fm contact by a carbon isotope excursion onset similar to the Sinemu-Pliens boundary event, while the other sequences fit with the a warm phase that lasts until the Davoei biozone. The Rotzo Formation represented the Carbonate Platform, being located over the Trento Platform and surrounded by the Massone Oolite, the Fanes Piccola Encrinite, the Lombadian Basin Medolo Group and Belluno Basin Soverzene Formation, and finally towards the south, deep water deposits of the Adriatic Basin. The Pliensbachian Podpeč Limestone of Slovenia, the Aganane Formation & the Calcaires du Bou Dahar of Morocco represent regional equivalents, both in deposition and faunal content.
The Budoš Limestone is a geological formation in Montenegro and maybe Albania, dating to 192-182 million years ago, and covering the Pliensbachian-Toarcian stage of the Jurassic Period. It is located within the High karst zone, and represents a unique terrestrial setting with abundant plant material, one of the few know from the Toarcian of Europe. It is the regional equivalent to the Toarcian-Aalenian units of Spain such as the Turmiel Formation and the El Pedregal Formation, the Sinemurian Coimbra Formation in Portugal, units like the Aganane Formation or the Tafraout Group of Morocco and others from the Mediterranean such as the Posidonia Beds of Greece and the Marne di Monte Serrone of Italy. In the Adriatic section, this unit is an equivalent of the Calcare di Sogno of north Italy, as well represents almost the same type of ecosystem recovered in the older (Pliensbachian) Rotzo Formation of the Venetian region and the Podpeč Limestone of Slovenia, know also for its rich floral record.
The Moltrasio Formation also known as the Lombardische Kieselkalk Formation is a geological formation in Italy and Switzerland. This Formation mostly developed in the Lower or Middle Sinemurian stage of the Lower Jurassic, where on the Lombardian basin tectonic activity modified the current marine and terrestrial habitats. Here it developed a series of marine-related depositional settings, represented by an outcrop of 550–600 m of grey Calcarenites and Calcilutites with chert lenses and marly interbeds, that recovers the Sedrina, Moltrasio and Domaro Formations. This was mostly due to the post-Triassic crisis, that was linked locally to tectonics. The Moltrasio Formation is considered a continuation of the Sedrina Limestone and the Hettangian Albenza Formation, and was probably a shallow water succession, developed on the passive margin of the westernmost Southern Alps. It is known due to the exquisite preservation observed on the Outcrop in Osteno, where several kinds of marine biota have been recovered.
The Coimbra Formation is a geological formation of Sinemurian age in the Lusitanian Basin of Portugal. The unit represents a series of peritidal to intertidal facies of a Carbonate platform mostly of Obtusum–Oxynotum age, that gradually evolve to open marine/hemipelagic units Vale das Fontes Formation and Lemede formation. This unit is known for its fossil content, including Invertertebrate and vertebrate ichnofossils and fossils.