Cañadón Asfalto Formation
The Cañadón Asfalto Formation is a Lower Jurassic to Middle Jurassic geologic formation, from the Jurassic period of the Mesozoic Era. Its age has been controversial, with uranium-lead dating of the volcanic tuff beds having given various different ages.[2] A Recent work suggested that the base of the formation was formed around 171 Ma, during the upper Aalenian, while the main age for the Lower Las Chacritas Member being around 168 Ma, during the Bajocian, Bathonian and Callovian While the overlying Puesto Almada Member seems to be around 158 ma, or Oxfordian age.[3] But that changed thanks to the discovery of zircons near the location of discovery of Bagualia, allowing a precise dating of Las Charcitas Member as Middle-Late Toarcian, 178-179 million years.[4] And a more advanced datation constraint the Age of the formation as Middle Toarcian-Lower Bajocian, being contemporaneous to the Chon Aike volcanic activity, being a local equivalent to Antarctica's Mawson Formation (Ferrar Volcanic Province) and the South African Drakensberg Group (Karoo Volcanic Province).[5] In the Antarctic Peninsula, the Volcanic-Lacustrine Sweeney Formation and the Anderson Formation (Ellsworth Land Volcanic Group, Latady Basin) are not only coeval but continuations of the biozone seen in the Chacritas member.[6]
Cañadón Asfalto Formation | |
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Stratigraphic range: Middle-Late Toarcian ~ Dubious assigantion of the Puesto Almada Member of likely Callovian-Oxfordian age, that can be part of the Cañadón Calcáreo Formation or the Sierra de la Manea Formation instead | |
![]() Cañadón Asfalto Formation near Cerro Cóndor, Chubut, Argentina | |
Type | Geological formation |
Unit of | Sierra de Olte Group |
Sub-units |
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Underlies |
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Overlies | Lonco Trapial Formation |
Thickness | 600 m (2,000 ft) |
Lithology | |
Primary | Sandstone |
Other | Limestone, shale, conglomerate, tuffite |
Location | |
Coordinates | 43.4°S 69.2°W |
Approximate paleocoordinates | 40.5°S 29.3°W |
Region | Chubut Province, Patagonia |
Country | Argentina |
Extent | Cañadón Asfalto Basin |
Type section | |
Named for | The Cañadón Asfalto in Chubut River region |
Named by | Stipanicic, P.N., Rodrigo, F.O.L., & Martínez, C.G[1] |
Year defined | 1968 |
![]() Formation map and location, shaded horizontally |
It is located in the Cañadón Asfalto Basin, a rift basin in Chubut Province of northwestern Patagonia, in southern Argentina.[7] The basin started forming in the earliest Jurassic.[8]
It is composed of fluvial-lacustrine deposits, typically sandstones and shales with a saline paleolake carbonate evaporitic sequence of limestone in its lowest Las Chacritas Member.[9] Interbedded with these are volcanic tuffites. It is divided into two members, the Las Chacritas Member, and the overlying Puesto Almada member, but the latter has also been assigned to the overlying Cañadón Calcáreo Formation by other authors.[10]
History
The study of the Cañadón Asfalto Basin Jurassic deposits started with Alejandro Matveievich Piatnitzky in 1936, that studied the zone from the Genoa River to the Chubut River, dividing several stratigraphic units, where he described the first layers that can be vinculated within the Cañadon Asfalfo Formation, the so-called "Capas de Estheria", recovered in places like the Cañón de Bagual, associated with plant remains such as Arthrotaxites, assignating them to the Jurassic interval.[11] His works were followed by several authors, but was M.A. Flores, in 1948–1957 on his study of the layers in between Chubut River, Sierra Cuadrada and Valle del Sapo, who defined these Estheria layers as bituminous Shales, finding on them Sauropod and floral remains, which led to the suggestion of referring to this section as the upper middle Jurassic.[12] In 1949, this Estheria unit was referred to the Sierra de Olte Group by J. Frenguelli, who also described some floral remains.[13] It was the team led by Stipanicic that named the Cañadón Asfalto Formation, referred back then as a Callovian-Oxfordian unit.[1] Following this definition, Tasch & Volkheimer did, in 1970, the main initial faunal review of the strata, with clear focus on the spinicaudatan fauna, with also the first regional correlations.[14] This work was followed by others such as C. Nakayama in 1972, F. Nullo & C. Proserpio in 1975 or J.M.C. Turner in 1983, all focused on geological aspects of the unit.[12] In 1979, Bonaparte did the first description of dinosaurian remains from the location, including Patagosaurus, Piatnitzkysaurus and Volkheimeria.[15] Towards the 90s, the Cañadón Asfalto was subdivided into lower and upper sections, with the older being equivalent of the Puesto Gilbert Formation and the upper coeval with the Cañadón Calcáreo Formation.[16] Latter in 2005, E.G. Figari, following his 1990's works, established the two actual members, calling them the lower and the upper member.[17] In 2012, these two were called the lower Las Chacritas Member and the upper Puesto Almada Member.[8] Recent works such as Cúneo et al. in 2013 have proven the formation is older, and that some of the sections that form the Puesto Almada member belong to the Cañadón Calcáreo Fm.[2] Beyond the U-Pb and Lu-Hf zircon datings, the main focus of the local works has been on the discovery on new fossil sites ("Canela" and "A12" sites, for example) and revision of both floral and faunal discoveries of rich older discovered ones (Specially on "Queso rallado" site).[5][8]
Geology

The Cañadón Asfalto Basin (whose full name is Somuncurá-Cañadón Asfalto rift basin) represents among the most extensive exposure of Jurassic rocks in South America. It limits to the northwest with the Subcordilleran Patagonian Batholith+Ñirihuau Basin and to the south with the Alto de Cotricó, a structural element that separates it from the San Jorge Gulf Basin.[8] It was developed over a Paleozoic basement, whose composition is dominated by plutonic and metamorphic rocks, that, along the Tria-Jurassic layers are part of a local succession of three megasequences, being the Jurassic ones linked with a mixed mosaic of volcanic (was likely linked to the Chon Aike Silicic Large Igneous Province) and sedimentary rocks (fluvial and lacustrine).[18] The Jurassic section can be correlated with an extensive tectonic regime for the central units in the basin, with also the presence of "pull-apart" models. This "pull-apart" model evolved based on the combined presence of diverse structural and depositional features that include lake-derived layer associated with vaporite horizons and various types of synsedimentary deformation, all with the presence of intercalations of basaltic strata. In this basin, towards the southern sector three microbasins are defined: Cerro Cóndor, Cañadón Calcáreo and Fossati.[8][19] The rotation of the Chubut Jurassic blocks is documented, yet the lateral components seem to have been linked to oblique extension.[19] The Chubut Province was in the Jurassic part of a local Rift that was a result of the fragmentation of Gondwana, associated in extension with the opening of the Weddell Sea and to the migration towards the south of the Antarctic Peninsula, developed in a similar way to the rift seen in the coeval deposits of the Transantarctic Mountains (Specially the Mawson Formation in the Queen Alexandra Rangue). This basin was latter affected by a regional contractional phase during the Early Cretaceous (seen in the deposition of the Chubut Group).[19]
Local vulcanism was linked with the Chon Aike Igneous Province, or Chon Aike-Antarctic Province. The Vulcanism was product of initial rifting, what also led to the Karoo-Ferrar (South Africa And Antarctica), where the Early Jurassic facies in Patagonia and Larsen Basin deposited influenced by the pushing the Wedell Sea basin did over the surrounding plates, as can be seen in the similarities between the Sweeney Formation and the Lonco Tapial Formation.[6] In the Cañadón Asfalto Fm is found on thin layers of tuffs produced by distal ash falls within the lacustrine layers of the lower Chacritas Member, with the presence of sectors with scarce pyroclastic flows and basaltic flows. The interdigitation between carbonate and volcaniclastic deposits is clearly evident in the surroundings of Estancia Fossatti and in the Navidad Sector.[8][18] Other Volcanic sectors nearby that may have influenced this formation include the Subcordilleran & Cordilleran Patagonian Batholiths in the west.[20]
Age
The Age of the sediments of the Cañadón Asfalto Formation has been debated for decades. It was initially Piatnitzky in 1939 who noted the over lain position of this sediments over the basement, and suggested possible Jurassic to Earliest Cretaceous age based on regional correlations. In the description of the Cañadón Asfalto Formation in 1968, Stipanicic et al. defined that both Cañadón Asfalto and Los Adobes where of "Dogger" (=middle Jurassic) age.[1] In 1984, there was a work that correlated the unit with the Ferrarotti successions, finding differences with the Cañadón Asfalto and upper layers lumped initially on it, suggesting there can be an Upper Jurassic or Lower Cretaceous distinctive unit.[21] Based on the Microfossils and flora, Toarcian to Callovian was assigned to Las Chacritas member, while Callovian-Tithonian was assigned to the Puesto Almada member.[19] However, this wasn't followed by the appearance of numerous radiometric datings obtained from outcrops from different depocenters: starting in 2007, where a K/Ar age of 170 ±4.4 Ma was obtain for the Las Chacritas Member, followed in 2010 of a younger 147.1 ± 3.3 Ma for the Puesto Almada Member, that was latter reassigned to 161 ± 3 Ma by U/Pb dating on zircons in the locality Estancia La Sin Rumbo.[19] Then, in 2013 Cúneo et al. provided the considered most controversial datations to date: Toarcian, 176,15 ± 0,12 and 178,766 ± 0,092 Ma at Cerro Bayo and Cerro Cóndor respectively, yet this was initially contested (with 168.2 ± 2.2 Ma for Chacritas member) and Puesto Almada constrained latter in 2017 to 160.3 ± 1.7-158.3 ± 1.3 Ma (Callovian-Oxfordian).[3] Yet, it was a more recent dating, the one that fully constrained Las Chacritas Member to Middle-Late Toarcian age (179,4 ± 0,059 Ma, 179,4 ± 0,13 Ma & 177,2 ± 0,4 Ma), age that was supported with the discovery of zircons of the same range in the Bagualia layers (Cañadón Bagual) and in other outcrops, incluing detailed age constraint in the uppermost level of the member proving a definitive age constraint of all the biota recovered in this layers to 179.17 ± 0.12 Ma-178.07 ± 0.21 Ma.[5][22] The Puesto Almada member is in a more complex situation, as seems some or all of its layers can belong on reality to the Cañadón Calcáreo Formation.[19] A separate unit in between the two has been even suggested, the Sierra de la Manea Formation, and this last one can include a great part of the Puesto Almada layers.[23]
Paleoenvironment
The Cañadón Asfalto formation represents a continuous inland sector on lacustrine and terrestrial habitats far from the nearest coast. The closest marine settings where recovered at the west in the Chubut Basin, where, for example the Toarcian Mulanguiñeu Formation recovers a diverse record of marine fauna, including index ammonites (Dactylioceras and Canavaria), brachiopods (groups Spiriferinida and Terebratulida), bivalves (families Nuculidae, Nuculanidae, Polidevciidae and Malletiidae), gastropods (families Eucyclidae, Trochoidea, Pseudomelanoidea, Cirridae, Procerithiidae, etc. ), calcareous tube annelids (Serpulidae), gregarious corals (Montlivaltia), decapods (Mecochirus robbianoi), crinoids (Pentacrinites), spines of Echinoidea, leaf remains (Elatocladus hallei; Conifers) and traces of bioturbation (ichnogenera Rhizocorallium and Lapispira), indicating that at this time the Paleopacific Ocean flooded the basin hosting benthic macroinvertebrate associations in a carbonate-elastic ramp, however, none of the measured transgressions flooded the Cañadón Asfalto Basin (although it is estimated that in the upper Toarcian the coast was very close to Paso de Indios), although it was influenced by the volcanic events of the latter, as shown by the traces of volcanic tuffs in the Toarcian part of the Paso de Indios formation.[24] Beyond this sector, the Ordovic-Devonian North Patagonian Massif and the Deseado Massif gave a montane influence to the deposition of the formation. This can be seen in the so-called "Navidad district section" recovers similar Pb isotopic compositions to the ores found on this massifs.[25] The Cañadón Asfalto Formation along with the Lonco Trapial Formation, Bajo Pobre Formation and Cañadón Huemules Formations in Argentina, and Mount Poster Formation & Sweeney Formation in Latady Basin, are part of the main mafic sectors of the Chon Aike-Antarctic Peninsula, being one of the largest rhyolitic provinces in the world, what is seen on the abundance of volcanic intrusions in the otherwise lacustine/terrestrial facies of the formation, what can be seen in the hyaloclastite and peperite facies of the Navidad sector, indicators of interaction of lacustrine waters and magmatic sources, that seem to come mostly from local basement rifts.[25][26]
Chacritas Member
This member is mostly made of two major depositional settings: lacustrine and fluvial deposits, that have intervals of tuffaceous materials, suggesting this environments coevolved with volcanic activity.[9] The lacustrine section has been called the "Chacritas Paleolake", and seems to have been a rather saline or even hypersaline hydrologically closed pan lake, shallow in deep, with marginal zones and palustrine subenvironments made of low-energy ramp-like margins.[27][26] This can be seen on several sections such as the Cañadón Carrizal, where layers that how aerial exposures, and so a regression tendency in a low-energy lake, what changued the biota locally (ex. microbial activity on surfaces).[27] The lacustrine facies can be seen in other locations, as in Quebrada de las Chacritas, where at least 5 types of different facies, with both lacustrine and Stromatolite bioherm origin where described, showing this last ones a microbial belt.[28] The increased amount of algal matter and microbial bioherms suggest highstand levels of the lake, while on layers where mudcracks and pedogenesis occurs shows likely a lowstand of the water level that killed the microbial matter.[28] It has been determined that the main lacustrine body existed in the so-called "Cerro Cóndor Biohermal Belt", while Cañadón Las Chacritas facies show progradations towards the south until it face basaltic materials in southern area of Cerro Cóndor, reflected in the flooding of the belt and increased algal fossils.[28] This lake was clearly influenced by the volcanic activity, as well was likely a product of the rifting that the Cañadón Asfalto basin suffered back in the Toarcian. This can bee seen on the abundance of chert like the one recovered in modern Lake Magadi in Kenyan section of the African Rift.[27] This chert is indicator of high alkaline settings in shallow lacustrine units, thus temporal increasing of Magadi-like mineralization in the lake may have been possible.[27] An identical type of lake, know as "Carapace Lake", also developed in a rift system was located in the coeval Mawson Formation of Antarctica, what suggest that both, Carapace and Chacritas where likely alkaline lakes that had notorious influence of hydrothermal fuids.[29] This type of lacustrine facies is seen also in the Antarctic Peninsula Sweeney Formation, that represents a continuation of the same Biozone both Lonco Tapial and Cañadón Asfalto are included.[6]
The abundance of organic matter in the lacustrine facies, great presence of microinvertebrate fauna together with the rare presence of mudcracks, low breccia presence and pedogeniclayers suggest that the immediate setting along the lake had between arid and sub-humid conditions. Nearby emerged settings have abundant Classopollis spp., key genera for thermophilic settings, what can suggest the nearby emerged lands had warm and dry conditions.[9] Other species suggest a warm to warm-temperate climate, with markedly seasonal (monsoonal) characteristics that coincide with the presence of the Seasonally Dry Subtropical Biome.[30] Overall this flora, as recovered in the Cañadón Lahuincó and Cañadón Caracoles sections suggest the presence of fluvial (riparian) and coastal lacustrine floras, along with inland dry settings dominated by Conifers, overall in a similar distribution that the one seen in coaeval layers in Australia, as well the Mawson Formation in Antarctica.[30] Data from local cuticles of Araucariaceous and Cheirolepidicaceous conifers have been put under microscope, what can lead to future deeper interpretations of local climate fluctuation.[31] Initial revisions of Brachyphyllum spp. cuticles has led to know the presence of common environmental stress on local conifers during the deposition of the Chacritas member.[32]
Puesto Almada Member
This member was originally described as being mostly a fluvial transition where the local lacustrine settings disappeared, yet, locations such as Cerro Bandera show that it hosted lacustrine, palustrine, and pedogenic deposits.[33] Alluvial facies are the main indicators of the sediment supply, while the lacustrine facies suggest a second water filling locally, where a smaller body of water know as "Almada Paleolake" was developed, creating also several coeval wetlands that are more notorious towards the uppermost section.[34] Tuff intrusions are more scarce than in the underlaying section and seem to be derived from ash directly falling into water.[33] Despite its name, the "Almada Fish Fauna", including genera such as Condorlepis groeberi, has been proven to belong to the Cañadón Calcáreo Formation, as well the crocodrilian genus Almadasuchus, all of this is due to the uncertain difference and limit between both units.[35] Overall climate conditions where similar to the underliying section, yet with a more marked seasonality and a more humid touch.[33]
Invertebrate fauna
Demospongiae
Palaeospongillidae reported from the Cañadon Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Palaeospongilla[9] |
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Isolated Specimens |
A Freshwater (Lacustrine) member of Palaeospongillidae (Spongillida Sponges). Represents the main lacustrine bottom inhabitant of the Chacritas Paleolake |
![]() Example of the living genus Spongilla. The genus Palaeospongilla was likely similar |
Crustacea
Crustacea reported from the Cañadon Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
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|
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Isolated Valves |
A Freshwater (Lacustrine) member of Eosestheriidae (Spinicaudatan). Originally identified as Cyzicus (Euestheria) taschi. This genus is found in identical alkaline lacustrine settings in the also Toarcian Mawson Formation of Antarctica |
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Isolated Valves |
A Freshwater (Lacustrine) member of Afrograptidae (Spinicaudatan). Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation. |
||
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|
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Isolated Valves |
A Freshwater (Lacustrine) member of Darwinulidae (Ostracod). |
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Isolated Valves |
A Freshwater (Lacustrine) member of Euestheriidae (Spinicaudatan). |
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Isolated Valves |
A Freshwater (Lacustrine) member of Fushunograptidae (Spinicaudatan). |
![]() Extant example of the Genus | |
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Isolated Valves |
A Freshwater (Lacustrine) member of Limnocytheridae (Ostracodan). Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation |
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|
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Isolated Valves |
A Freshwater (Lacustrine) member of Loxoconchidae (Ostracodan). Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation. |
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|
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Isolated Valves |
A Freshwater (Lacustrine) member of Darwinulidae (Ostracodan). Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation. |
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Pseudestherites[33] |
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|
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Isolated Valves |
A Freshwater (Lacustrine) member of Antronestheriidae (Spinicaudatan). Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation. |
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|
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Isolated Valves |
A Freshwater (Lacustrine) member of Cytheroidea (Ostracodan). Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation. |
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|
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Isolated Valves |
A Freshwater (Lacustrine) member of Limnocytheridae (Ostracodan). Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation. |
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Wolfestheria[37] |
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|
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Isolated Valves |
A Freshwater (Lacustrine) member of Fushunograptidae (Spinicaudatan). |
|
Mollusca
Mollusca reported from the Cañadon Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
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Isolated Shells |
A Freshwater (Lacustrine) member of Corbiculidae (Bivalve). |
![]() Extant example of the Genus | |
Cyanocyclas[41] |
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|
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Conchas Aisladas |
Un miembro de agua dulce (lacustre) de Corbiculidae (Bivalvo). |
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Isolated Shells |
A Freshwater (Lacustrine) member of Unionidae (Bivalve). The most abundant Bivalve genus on the Formation. Represents also some of the smallest-sized specimens recorded in the Mesozoic |
![]() Extant example of the Genus | |
Nayadidae[13] |
Indeterminate |
|
|
Isolated Shells |
A Freshwater (Lacustrine) member of Unionidae (Bivalve). |
|
|
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|
Isolated Shells |
A Freshwater (Lacustrine) member of Tateidae (Snail). |
![]() Extant example of the Genus | |
Sphaeridae[26] |
Indeterminate |
|
|
Isolated Shells |
A Freshwater (Lacustrine) member of Sphaeriida (Bivalve). |
|
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Isolated Shells |
A Freshwater (Lacustrine) member of Viviparidae (Snail). |
![]() Extant example of the Genus | |
Insecta
Insect eggs of unknown affinity were reported from several layers of the Estancia Fossati locality.[9]
Insects reported from the Cañadon Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Indeterminate |
|
|
Head capsules |
Indeterminate Bittacidae (Migdes) remains, associated with lacustrine facies. Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation |
![]() Extant member of the Family | |
Indeterminate |
|
|
Elytra and body remains |
Indeterminate Beetle remains, associated with lacustrine facies |
![]() Extant example of the Group | |
Conchindusia isp. |
|
|
Imprints or compressed moulds of larval cases |
Indeterminate Trichoptera (Caddisflies) Ichnofossils, associated with lacustrine facies |
||
Indeterminate |
|
|
Fragmentary wings |
Indeterminate Heteroptera remains, associated with lacustrine facies |
![]() Extant example of the Group | |
Neorthophlebidae[43] |
Indeterminate |
|
|
Wings and parts of body |
Indeterminate Bittacidae (Scorpionfly) remains, associated with lacustrine facies. Given the stratigraphic uncertainty, it may come from the Cañadón Calcáreo Formation |
|
Ostracindusia isp. |
|
|
Imprints or compressed moulds of larval cases |
Indeterminate Trichoptera (Caddisflies) Ichnofossils, associated with lacustrine facies |
||
Terrindusia isp. |
|
|
Imprints or compressed moulds of larval cases |
Indeterminate Trichoptera (Caddisflies) Ichnofossils, associated with lacustrine facies |
||
Indeterminate |
|
|
Wings and larval cases |
Indeterminate Trichoptera (Caddisflies) remains, associated with lacustrine facies |
![]() Extant example of the Group | |
Vertebrate fauna
Fish
Actinopteri reported from the Cañadon Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Indeterminate |
|
|
Isolated large median fin & Isolated Scales |
A Freshwater (Lacustrine) member of Archaeomaenidae (Teleostei). Maybe related with the genus Oreochima, coming from layers coeval, coregional and of identical deposition of the Mawson Formation of Antarctica |
![]() Example of member of the family Archaeomaenidae, Archaeomaene | |
Amphibians
Amphibians reported from the Cañadon Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
|
Las Chacritas Member |
|
An early frog of the family Notobatrachidae. Notobatrachus degiustoi can be distinguished from N. reigsi by features of the skull. The presence of this anuran inseveral locations suggest local proliferation linked with lacustrine bodies |
| ||
Turtles
Turtles reported from the Cañadon Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
|
|
Las Chacritas Member |
|
A stem turtle (Mesochelydian) outside both extant groups, closely related with Kayentachelys aprix of North America and Indochelys spatulata of India. Likely occupied aquatic or semiaquatic niches.[51] |
||
Indeterminate |
|
Las Chacritas Member |
|
Indeterminate Turtle remains |
||
Lepidosaurs
Lepidosaurs reported from the Cañadon Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Sphenocondor[53] |
Sphenocondor gracilis |
Queso Rallado |
Las Chacritas Member |
Dentary |
A Sphenodontian Rhynchocephalian, closely related with Godavarisaurus from the almost coeval Jurassic Kota Formation of India, maybe part of an endemic Gondwanan clade.[53] |
Crocodylomorpha
Crocodyliformes reported from the Cañadón Asfalto Formation | ||||||
---|---|---|---|---|---|---|
Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Indterminate |
Queso Rallado |
Las Chacritas Member |
Several isolated remains |
Indeterminate crocodylomorph remains that represent among the most complete vertebrates linked with lacustrine facies. |
Pterosaurs
Pterosaurs reported from the Cañadón Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Allkaruen koi |
Canadón Carrizal |
Las Chacritas Member |
A braincase, as well as a mandible and cervical vertebrae. |
A Pterosaur either related with Breviquartossa or maybe even a sister group of monofenestratan (Wukongopteridae + Pterodactyloidea) pterosaurs |
| |
Indeterminate |
Las Chacritas |
Las Chacritas Member |
Uncatalogued specimens, several mandibles, braincase, shoulder girdle, two humeri, several wing-finger phalanges |
Indeterminate remains of a pterosaur, possibly a Rhamphorhynchoidea. It seems to represent a rhamphorhynchoid pterosaur with a wingspan of about 1.5–2 meters. The morphology is very similar to that of the lower jaw of the Scaphognathinae.[57] |
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Theropods
Theropoda reported from the Cañadón Asfalto Formation | ||||||
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Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Asfaltovenator vialidadi |
Cerro Condor |
Las Chacritas Member |
Nearly compete skull and largely complete front half of the skeleton forward of the hips, distal pubis and fermur and proximal fibula and tibia, partial foot |
A probable early member of Allosauroidea |
| |
Indeterminate |
|
Las Chacritas Member |
Isolated teeth: MPEF BA 182/08, BA 40/08, BA 09/80, BA 88/08, BA 252G+165/08 A, BA 252G+165/08 B, BA 252G+165/08 C |
Theropod dinosaur teeth that wear resemblance with those assigned to the families Ceratosauridae, Megalosauridae and Abelisauridae |
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Indeterminate |
Cerro Cóndor |
Las Chacritas Member |
A dentary with teeth in situ, MPEF-PV 6775 |
It resembles the dentary of Ceratosaurus |
||
Condorraptor currumili |
Las Chacritas |
Las Chacritas Member |
Partial articulated skeleton |
A relative of Piatnitzkysaurus from the same formation, and a possible junior synonym of it as well. |
| |
Indeterminate |
|
Las Chacritas Member |
Isolated Teeth: MEPF BA 61/08, BA 103/08, BA 32/08 A, BA 32/08 B, BA 104/08, BA 226B/08, PV 3498, BA 29/08, BA51/08, BA 270/08 a, BA 270/08 b, BA 270/08 c |
Theropod dinosaur teeth that wear resemblance with those assigned to the family Dromaeosauridae. Alternatively, they could belong to basal members of Coelurosauria |
||
Eoabelisaurus mefi |
Jugo Luco |
Las Chacritas Member |
A nearly complete articulated skeleton |
A Neoceratosaur, that was suggested to be a basal member of Abelisauria, but also a member of Ceratosauridae |
| |
Indeterminate |
|
Las Chacritas Member |
Isolated Teeth: MPEF PV 1175, BA 66/08, PV 1356, PV 1357 |
Theropod dinosaur teeth that wear resemblance with those assigned to the family Megalosauridae. |
||
Basal Neotheropoda[59] |
Indeterminate |
|
Las Chacritas Member |
Isolated Teeth: MPEF BA 68/08, BA 92/08, PV 3499, BA 68/08, BA 183/08 |
Theropod dinosaur teeth that wear resemblance with those assigned to basal neotheropods, such as members of Coelophysoidea. |
|
Indeterminate |
|
Las Chacritas Member |
Isolated Teeth & Cranial remains: MPEF 1717 CC 205, PV 3440A A, PV 3440A B, PV 3440A C, PV 3440A D, PV 3440A E, PV 3440A F, PV 3440A G |
Theropod dinosaur teeth that have resemblance with those assigned to members of Piatnitzkysauridae. |
||
Piatnitzkysaurus floresi |
Cerro Cóndor South |
Las Chacritas Member |
Two "fragmentary skulls with associated postcranium."[64] |
Possible senior synonym of Condorraptor from the same formation. |
| |
Indeterminate |
|
Las Chacritas Member |
Isolated Teeth : MEPF PV 1350 |
Theropod dinosaur teeth resembling those assigned to members of Spinosauridae. Alternatively, they could belong to members of Ceratosauria |
||
Indeterminate |
|
Las Chacritas Member |
Isolated Teeth : MEPF BA 84/08, BA 49/08 A, BA 49/08 B, BA 64/08, BA 65/08, BA 266/07 |
Theropod dinosaur teeth that wear resemblance with those assigned to members of Megalosauridae and Dromaeosauridae |
||
Indeterminate |
|
Las Chacritas Member |
Isolated Teeth : MPEF PV 1640 |
"Outlier" tooth that doesn't fit in any previously know morphotype, maybe due to preservation |
||
Theropodipedia[65] |
Theropodipedia ichnog. indeterminate |
|
Las Chacritas Member |
Footprints |
Possible theropod footprints, unassigned to any concrete ichnogenus |
|
Sauropodomorphs
Sauropodiformes reported from the Cañadón Asfalto Formation | ||||||
---|---|---|---|---|---|---|
Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Bagualia alba |
Cañadon Bagual |
Las Chacritas Member |
The partial skeletons of three individuals |
An early member of Eusauropoda, related with the African genus Spinophorosaurus |
||
Indeterminate |
Cerro Condor Sur |
Las Chacritas Member |
MACN-CH 934: axial neural arches and spines, an ilium, a pubis, ?two or ?three ischia, and two maxillae |
This specimen shows strong Diplodocidae affinities, yet it has been considered either a derived non-neosauropodan eusauropod (having resemblance with Lapparentosaurus in some characters) or even a basal neosauropod ( also resembling with Haplocanthosaurus) |
||
Indeterminate |
Cerro Condor Sur |
Las Chacritas Member |
MACN-CH 230: three dorsal vertebrae |
Likely a eusauropod With strong resemblance with the Asian genus Klamelisaurus, this specimen was defined as a ‘dwarf-type’ sauropod feeding on lower/different vegetation |
||
Patagosaurus fariasi |
Cerro Condor |
Las Chacritas Member |
Many specimens, including a partial skull. |
A non-neosauropodan eusauropodan member of Cetiosauridae. This genus represents the most abundant sauropod in the formation |
| |
Indeterminate |
Cañadon Bagual |
Las Chacritas Member |
Isolated Teeth: MPEF-PV 10860 |
An indeterminate Sauropodiform or a very basal Sauropod or even dental material of Volkheimeria.[71] |
||
Indeterminate |
Cerro Condor Sur |
Las Chacritas Member |
MACN-CH 219, 223(+221), 231 |
Too fragmentary to be ascribed to any taxon, for now classified as Sauropoda indet. |
||
Indeterminate |
Queso Rallado, near Cerro Cóndor |
Las Chacritas Member |
Isolated Teeth: MPEF-PV 10606 |
An indeterminate Titanosauriform. It can be alternatively a basal Eusauropod. Possible relationships with Atlasaurus |
||
Volkheimeria chubutensis |
Cerro Cóndor South |
Las Chacritas Member |
"Partial skeleton consisting of presacral and sacral vertebrae, pelvis, [and] hindlimb." |
Either a gravisaur or a sister taxon of the Indian genus Barapasaurus |
||
Ornithischians
Ornithischians reported from the Cañadón Asfalto Formation | ||||||
---|---|---|---|---|---|---|
Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Indeterminate |
Queso Rallado |
Las Chacritas Member |
Isolated ungual phalanx and Isolated Teeth: MPEF-PV 3818, MPEF-PV 3824, MEPF-PV 3820, MEPF-PV 3825, MEPF-PV 10861, MPEF-PV 10823, MPEF-PV 3821 & MPEF-PV 10864 |
An indeterminate Cerapodan with resemblances with Hypsilophodon |
||
Indeterminate |
Queso Rallado |
Las Chacritas Member |
Metapodials, caudal vertebrae and isolated phalanges: MPEF-PV 3826 |
heterodontosaurid that cannot be compared with Manidens due to the lack of overlapping fossils. |
||
Manidens condorensis |
|
Las Chacritas Member |
Partial articulated specimen, skull & associated elements as well referred isolated teeth: MPEF-PV 3809, MPEF-PV 3211, MPEF-PV 3808, MPEF-PV 10867, MPEF-PV 1719, MPEF-PV 1786, MPEF-PV 1718, MPEF-PV 3810, MPEF-PV 3811, MPEF-PV 3812, MPEF-PV 3813, MPEF-PV 3814, MPEF-PV 3815, MPEF-PV 3816, MPEF-PV 10866 |
A primitive and small heterodontosaurid. |
| |
Indeterminate |
|
Las Chacritas Member |
Isolated teeth: MPEF-PV 3817, MPEFPV 3819, MPEF-PV 3822. |
Not referable to any taxa beyond Ornithischia Indet. |
||
Mammals
Mammals reported from the Cañadón Asfalto Formation | ||||||
---|---|---|---|---|---|---|
Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
Indeterminate |
Queso Rallado |
Las Chacritas Member |
Isolated Teeth |
An Allotherian whose affinities hasn't been tested |
||
Argentoconodon fariasorum |
Queso Rallado |
Las Chacritas Member |
MPEF-PV2362, fragmentary left maxilla, MPEF-PV2363 partial skeleton, MPEFPV2364 isolated complete right upper last molariform |
A volaticotherian (Alticonodontinae), closely related with the Asian genus Volaticotherium, having similar postcraneal appaerance, indicating possible gliding capabilities, yet better material is needed to prove it.[76] |
||
Asfaltomylos patagonicus |
Queso Rallado |
Las Chacritas Member |
MPEF PV 1671, complete lower maxilla |
An Australosphenidan, related to Henosferus in Henosferidae. |
||
Condorodon spanios |
Queso Rallado |
Las Chacritas Member |
MPEF-PV 2365, isolated complete lower left molariform |
An "amphilestid" triconodont, related with the late jurassic African Tendagurodon.[75] |
||
|
|
Las Chacritas Member |
MPEF 2353 right lower jaw, MPEF 2354 Left lower jaw, MPEF 2357 Left lower jaw, referred MPEF 2355 isolated upper premolar |
An Australosphenidan, related to Asfaltomylos in Henosferidae, being twice as large as this last one.[78] |
||
Fungi
Genus | Species | Location | Stratigraphic position | Member | Material | Ecogroup | Palaeoclimate requirements | Notes |
---|---|---|---|---|---|---|---|---|
Annella[79] |
|
Central Patagonia |
|
|
Hypae and Miospores |
Unknown: either Aquatic (Freshwater) or Parasitic |
Unknown, suggested highly seasonality |
A Fungus of uncertain relationships. This species is recovered in both coal seams and proximal prodelta sediments, making the assignation of a biome complex.[79] |
Plant remains
Palynology
According to a palynological study the dominant pollen was produced by the conifer families Cheirolepidiaceae (Classopollis) and Araucariaceae (mainly Araucariacites and Callialasporites), suggesting that warm-temperate and relatively humid conditions under highly seasonal climate prevailed during the depositional times of the unit. The abundance of Botryococcus supports the presence of a shallow lake with probably saline conditions.[80] Locally, the Cañadón Asfalto represents a more poor record of the floras seen in the undeliying Lonco Tapial Formation, with its closest floras found on the Antarctic Peninsula Sweeney Formation at Potter Peak, sharing Brachyphyllum spp. and Elatocladus confertus.[6]
Genus | Species | Location | Stratigraphic position | Member | Material | Ecogroup | Palaeoclimate requirements | Notes |
---|---|---|---|---|---|---|---|---|
|
Central Patagonia |
|
|
Algae |
Aquatic (Freshwater); Alkaline indicator |
Highly seasonal climate |
A Freshwater algae of the family Botryococcaceae. This genus is the main indicator, due to its abundance, of the presence of a shallow lake with probably saline conditions, reaching in some samples about 96 to 70%.[80] | |
|
Central Patagonia |
|
|
Zygospores |
Aquatic (Freshwater) |
Temperate to warm; seasonal climate |
Algae of the family Zygnemataceae | |
|
Central Patagonia |
|
|
Zygospores |
Aquatic (Freshwater) |
Temperate to warm; seasonal climate |
Algae or Algae Acritarch of the family Prasinophyceae. | |
|
Central Patagonia |
|
|
Spores |
Upland and Riverside |
Can withstand long periods of drought; seasonal climate |
Affinities with Bryophyta. | |
Antulsporites[80] |
|
Central Patagonia |
|
|
Spores |
Upland and Riverside |
Can withstand long periods of drought; seasonal climate |
Affinities with the family Sphagnaceae in the Sphagnopsida. "Peat moss" spores, related to genera such as Sphagnum that can store large amounts of water. |
Stereisporites[80] |
|
Central Patagonia |
|
|
Spores |
Upland and Riverside |
Can withstand long periods of drought; seasonal climate | |
Neoraistrickia[80] |
|
Central Patagonia |
|
|
Spores |
Upland and Lowland |
Warm to temperate, relatively wet |
Affinities with the family Selaginellaceae and Lycopodiaceae in the Lycopsida. |
Retitriletes[80] |
|
Central Patagonia |
|
|
Spores |
Upland and Lowland |
Warm to temperate, relatively wet | |
Clavatisporites[80] |
|
Central Patagonia |
|
|
Spores |
Lowland and Riverside |
Warm to temperate, relatively wet |
Filicopsida incertae sedis |
Obtusisporis[80] |
|
Central Patagonia |
|
|
Spores |
Lowland and Riverside |
Warm to temperate, relatively wet | |
Cadargasporites[80] |
|
Central Patagonia |
|
|
Spores |
Lowland and Riverside |
Warm to temperate, relatively wet |
Uncertain affinity Fern Spores |
Ischyosporites[80] |
|
Central Patagonia |
|
|
Spores |
Upland, Lowland Riverside |
Warm to temperate, relatively wet |
Affinities with the family Lygodiaceae and Schizaeaceae in the Polypodiopsida. Climbing or herbaceous fern spores. |
Klukisporites[80] |
|
Central Patagonia |
|
|
Spores |
Upland, Lowland Riverside |
Warm to temperate, relatively wet | |
Baculatisporites[81] |
|
Central Patagonia |
|
|
Spores |
Lowland and Riverside |
Warm to temperate, relatively wet |
Affinities with the family Osmundaceae in the Polypodiopsida. Near fluvial current ferns, related to the modern Osmunda regalis. |
Rugulatisporites[81] |
|
Central Patagonia |
|
|
Spores |
Lowland and Riverside |
Warm to temperate, relatively wet | |
Verrucosisporites[81] |
|
Central Patagonia |
|
|
Spores |
Upland |
Can withstand long periods of drought; seasonal climate | |
Todisporites[81] |
|
Central Patagonia |
|
|
Spores |
Upland |
Warm to temperate, relatively wet. Can withstand long periods of drought; seasonal climate | |
Trilobosporites[80] |
|
Central Patagonia |
|
|
Spores |
Upland, Lowland and Riverside |
Warm to temperate, relatively wet |
Affinities with the families Cyatheaceae/Dicksoniaceae Dipteridaceae/Matoniaceae in the Polypodiopsida. |
Deltoidospora[80] |
|
Central Patagonia |
|
|
Spores |
Upland, Lowland and Riverside |
Warm to temperate, relatively wet | |
|
Central Patagonia |
|
|
Spores |
Lowland and Riverside |
Warm to temperate, relatively wet | ||
Biretisporites[80] |
|
Central Patagonia |
|
|
Spores |
Lowland and Riverside |
Warm to temperate, relatively wet |
Affinities with the Marattiaceae in the Polypodiopsida. Fern spores from low herbaceous flora. |
|
Central Patagonia |
|
|
Pollen |
Riverside |
Warm, can withstand long periods of drought; seasonal climate |
Affinities with the families Peltaspermaceae, Corystospermaceae or Umkomasiaceae in the Peltaspermales. Pollen of uncertain provenance that can be derived from any of the members of the Peltaspermales. | |
Vitreisporites[80] |
|
Central Patagonia |
|
|
Pollen |
Riverside |
Warm, relatively wet |
From the family Caytoniaceae in the Caytoniales. Caytoniaceae are a complex group of Mesozoic fossil floras that may be related to both Peltaspermales and Ginkgoaceae. |
|
Central Patagonia |
|
|
Pollen |
Lowland and Riverside |
Warm to temperate, can withstand long periods of drought; seasonal climate |
A Pollen Grain, affinities with Ephedraceae inside Gnetopsida. | |
|
Central Patagonia |
|
|
Pollen |
Upland, Lowland and Riverside |
?Warm to temperate, relatively wet |
Affinities with the family Araucariaceae in the Pinales. Conifer pollen from medium to large arboreal plants. | |
|
Central Patagonia |
|
|
Pollen |
Upland, Lowland and Riverside |
?Warm to temperate, relatively wet | ||
Inaperturopollenites[80] |
|
Central Patagonia |
|
|
Pollen |
Upland, Lowland and Riverside |
?Warm to temperate, relatively wet | |
Pinuspollenites[80] |
|
Central Patagonia |
|
|
Pollen |
Upland, Lowland and Riverside |
?Warm to temperate, relatively wet |
Affinities with the family Pinaceae in the Pinopsida. Conifer pollen from medium to large arboreal plants. |
|
Central Patagonia |
|
|
Pollen |
Upland, Lowland and Riverside |
?Warm to temperate, relatively wet |
Affinities with both Sciadopityaceae and Miroviaceae in the Pinopsida. This pollen's resemblance to extant Sciadopitys suggest that Miroviaceae may be an extinct lineage of Sciadopityaceae-like plants.[82] | |
|
Central Patagonia |
|
|
Pollen |
Lowland and Coastal lake |
Warm to temperate, can withstand long periods of drought; seasonal climate |
Affinities with the Hirmeriellaceae in the Pinopsida. Classopollis is the most abundant component of the assemblage, with ranges from 73 to 81.6% to 89.6%-89.7% in some samples.[80] | |
Exesipollenites[81] |
|
Central Patagonia |
|
|
Pollen |
Lowland and Coastal lake |
Warm to temperate, can withstand long periods of drought; seasonal climate | |
Perinopollenites[81] |
|
Central Patagonia |
|
|
Pollen |
Lowland and Coastal lake |
Warm to temperate; seasonal climate |
Affinities with the family Cupressaceae in the Pinopsida. Pollen that resembles that of extant genera such as the genus Actinostrobus and Austrocedrus, probably derived from Upland environments. |
Phrixipollenites[81] |
Phrixipollenites sp. |
Central Patagonia |
|
|
Pollen |
Upland |
Temperate, relatively dry |
Affinities with the family Podocarpaceae. Pollen from diverse types of Podocarpaceous conifers, that include morphotypes similar to the low arbustive Microcachrys and the medium arbustive Lepidothamnus, likely linked with Upland settings |
|
Central Patagonia |
|
|
Pollen |
Upland |
Temperate, relatively dry | ||
Podosporites[80] |
|
Central Patagonia |
|
|
Pollen |
Upland |
Temperate, relatively dry | |
Podosporites[80] |
|
Central Patagonia |
|
|
Pollen |
Upland |
Temperate, relatively dry | |
|
Central Patagonia |
|
|
Pollen |
Upland |
Temperate, relatively dry | ||
Macroflora
Genus | Species | Location | Stratigraphic position | Member | Material | Notes | Images |
---|---|---|---|---|---|---|---|
|
Central Patagonia |
|
|
Stems |
Plants of the group Equisetales. Usually linked with riversides |
![]() Equisetites specimen | |
|
Central Patagonia |
|
|
Isolated Pinnae |
Plants of the family Osmundaceae. |
| |
Gleichenites[84] |
|
Central Patagonia |
|
|
Isolated Pinnae |
Plants of the family Gleicheniales. |
|
|
Central Patagonia |
|
|
Isolated Pinnae |
Plants of the group Sphenopteridae, whose affinity for mesozoic specimens is uncertain, yet has been suggested to be fronds of Dicksoniaceae affinity |
| |
Archangelskya furcata |
Central Patagonia |
|
|
Isolated Pinnae |
Plants of the group Pteridospermata |
||
Lepidopteris scassoi |
Central Patagonia |
|
|
Isolated Pinnae |
Plants of the group Peltaspermaceae. This species represents the youngest record of the genus, by more than 20 Myr. |
| |
Peltaspermum sp. |
Central Patagonia |
|
|
Ovuliferous Cones |
Plants of the group Peltaspermaceae. |
| |
|
Central Patagonia |
|
|
Leaflets |
Affinities with Bennettitales inside Cycadeoidopsida. |
| |
|
Central Patagonia |
|
|
Pollen Organs |
Plants of the group Leptostrobales (Czekanowskiales). Gingko-like taxa |
||
|
Central Patagonia |
|
|
Pollen Organs |
Incertae sedis inside Coniferales. Some specimens are difficult to identify. |
||
|
Central Patagonia |
|
|
Ovuliferous scales |
Plants of the family Araucariaceae. |
||
|
Central Patagonia |
|
|
Branched shoots |
Plants of the family Araucariaceae or Cheirolepidiaceae |
||
|
Central Patagonia |
|
|
Branched shoots & Ovuliferous cones |
Plants of the family Araucariaceae or Cheirolepidiaceae |
||
Brachyoxylon currumilii |
Central Patagonia |
|
|
Fossil Wood |
Plants of the family Araucariaceae or Cheirolepidiaceae |
||
|
Central Patagonia |
|
|
Branched shoots |
Plants of the family Cupressaceae |
||
|
Central Patagonia |
|
|
Branched shoots & Ovuliferous cones |
Plants of the family Cunninghamioideae. Along with the also Argentinian species A. minuta, this specimens represent the oldest fossil taxa that can be confidently assigned to Cupressaceae sensu lato |
||
|
Central Patagonia |
|
|
Branched shoots |
Plants of the family Taxodiaceae |
||
See also
References
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