Agua de la Piedra Formation | |
Type: | Geological formation |
Age: | Late Oligocene (Deseadan) ~ |
Period: | Chattian |
Prilithology: | Tuff |
Otherlithology: | Paleosols |
Namedby: | Gorroño et al. |
Year Ts: | 1979 |
Region: | southern Mendoza Province |
Country: | Argentina |
Coordinates: | -36.6°N -69.7°W |
Paleocoordinates: | -37.8°N -62.9°W |
Unitof: | Malargüe Group |
Subunits: | "Rodados Lustrosos" level |
Underlies: | alluvium |
Overlies: | Pircala-Coihueco Formation |
Thickness: | 37m (121feet) (tuffs) |
Extent: | southernmost Precordillera northernmost Neuquén Basin |
Location Ts: | Quebrada Fiera, Malargüe |
Coordinates Ts: | -36.5537°N -69.701°W |
Region Ts: | Mendoza Province |
Country Ts: | Argentina |
Thickness Ts: | 37m (121feet) (tuffs) |
The Agua de la Piedra Formation (FAP, Spanish names include Estratos de Agua de la Piedra and Complejo Volcano-sedimentario del Terciario inferior)[1] is a Late Oligocene (Deseadan in the SALMA classification) geologic formation of the Malargüe Group that crops out in the southernmost Precordillera and northernmost Neuquén Basin in southern Mendoza Province, Argentina.[2]
The strictly terrestrial tuffs and paleosols of the formation, geologically belonging to Patagonia, have provided a wealth of mammal fossils of various groups at Quebrada Fiera, including Mendozahippus fierensis, Pyrotherium, Coniopternium and Fieratherium. Terror birds reminiscent of the terror bird Andrewsornis and indeterminate remains of the phorusrhacid family have found in conjunction with the mammals.
The Agua de la Piedra is geologically part of the Neuquén Basin, Argentina's most prolific onshore petroleum producing basin of northwestern Patagonia, and crops out in the geographical feature of the Andean orogeny; the Argentinian Precordillera of the higher Andes in the hinterland. The Malargüe Group, of which the Agua de la Piedra Formation is the uppermost unit, hosts among the most spectacular dinosaur fossils and nesting sites in the Allen Formation, the lowermost stratigraphic unit of the group.
The Jagüel Formation, overlying the Allen Formation, hosts the Cretaceous–Paleogene boundary and has provided fossils of marine reptiles including mosasaurs[3] and the marine turtle Euclastes meridionalis. The Roca Formation, overlying the Jagüel Formation shows evidence of Atlantic waters depositing the evaporites, claystones and limestones of the formation.[4] [5]
The Neuquén Basin started forming in the latest Jurassic as one of the rift basins resulting from the break-up of Pangea. While the earlier formations in the basin are mostly distal terrestrial in nature, the Agua de la Piedra Formation is a unique combination of purely terrestrial influence (paleosols) with the early Andean volcanism in the form of tuffs.
Oligocene South America differed quite substantially from the Eocene period preceding it. Isolated from Gondwana for 70 million years, the continent had developed widespread lush forests with their own specific faunas. The climate drastically cooled at the Eocene-Oligocene boundary with global cooling as a result of the formation of the Antarctic Ocean current. The South American landscape became more arid than in the Eocene with ongoing volcanism related to the Andean orogeny affecting the local climates.
The Oligocene of South America is characterized by the arrival of the first monkeys, possibly rafting from Africa, which in the Oligocene was significantly removed from South America. The first rodents had arrived to the island continent in the Late Eocene before,[6] perhaps using similar methods of transoceanic transport. The rodents of South America diversified in the Oligocene. Cabeza Blanca, where the Sarmiento Formation outcrops, has provided the richest and most diverse Oligocene fauna of South America.[7]
The cooler Oligocene climate led to the widespread extension of savanna and other grassland biomes. In the Early Oligocene, these rodents inhabited open and arid landscapes with wind-blown dust and grasslands environments.[8]
The oldest confirmed New World monkey fossils stem from the Deseadan formations Salla in presently Andean Bolivia (the approximately 1000g weighing Branisella boliviana and Szalatavus attricuspis half the size of Branisella) and the 2000g heavy Canaanimico from the Chambira of Amazonian Peru.[9]
The rodents had arrived in the Late Eocene and diversified greatly during the Deseadan following the appearance of Andemys with species A. frassinettii and A. termasi in the Tinguirirican (Abanico Formation; Tinguiririca fauna). Caviomorphs arrived in Patagonia during the latest Eocene or early Oligocene, andby the Late Oligocene they were highly diversified, with representatives of the four main lineages. A great morphological disparity, at least in tooth morphology, was then acquired mainly by the development of hypsodonty in several lineages. The early evolution of each of the major clades was complex, especially for chinchilloids and octodontoids. The first stages of the evolution of cavioids are more obscure because they are recognized through the relatively derived Deseadan species of Cavioidea.[10]
The Oligocene (Tinguirirican and Deseadan SALMAs plus La Cantera fauna) has a rich record of caviomorphs showing a greater morphological disparity than older faunas. Representatives of the four superfamilies, with the archetypal dental features that characterize species of the subsequent SALMAs, can be clearly recognized, at least since the Deseadan SALMA. Although a few genera (e.g., Andemys, Branisamys) cannot be assigned with certainty to any supra generic taxa. The Acaremyidae were likely a group of austral differentiation. The first representatives, the Deseadan Platypittamys brachyodon, Galileomys baios and Changquin woodi,[11] attest to its differentiation into several lineages.[12]
Early Andean volcanism in the Southern Cone of South America dating to the Oligocene has been found in:
The formation comprises the "Rodados Lustrosos" level, formed by clastic heterogeneous conglomerates in a silty matrix, considered as the stratigraphic evidence of the Pehuenche orogenic phase of the Andean orogeny, followed by uniform sequences, variable in thickness, of whitish-ocher tuffaceous paleosols with concretions and whitish-gray tuffs with intercalations of pyroclastic deposits.[19]
The upper part of the Agua de la Piedra Formation consists of 37m (121feet) of white-grayish tuffs and tobaceous paleosols, with laminated or massive parallel stratification constitute the fossiliferous level of Quebrada Fiera.[20] The formation overlies the Pircala-Coihueco Formation.
The studied profiles of the Agua de la Piedra Formation show large lateral lithological varieties, typical of alluvial fan depositional setings. The climate during deposition has been estimated to be semi-arid and the differential thicknesses of facies associations within the Agua de la Piedra Formation may represent the infill of minibasins in the forming foreland of the Andes. Sedimentary loading can enhance the effect of tectonic forces in foreland basins. The variety in volcanic fragments and composition indicates local ash fall caused by contemporaneous volcanism in the area of deposition.[21]
2017 research on the Deseadan fauna (late Oligocene) from Quebrada Fiera, south of Mendoza Province, Argentina, evidences a rich mammal assemblage that shows the existence of common elements with Deseadan faunal associations of Patagonia and those of lower latitudes such as Salla, Bolivia, as well as endemic taxa of different groups.[22]
Endemism refers to Notohippidae (Mendozahippus fierensis), Leontiniidae (Gualta cuyana), Homalodotheriidae (Asmodeus petrasnerus) and Metatheria(Fieratherium sorex); to these mammals a new terrestrial snail has been added in 2016.[23]
Faunal data published in 2019 confirm the Deseadan age, but as per 2020, absolute dating is lacking for Quebrada Fiera.[19]
The Quebrada Fiera site is situated in the Malargüe Department,[24] southern Mendoza Province, Argentina, in the foothills of the Andes Range. The fossiliferous levels are located at around -36.5537°N -69.701°W at 1300mto1406mm (4,300feetto4,613feetm) elevation. The site was discovered during a geological prospection carried out by Yacimientos Petrolíferos Fiscales (YPF) in the late 1970s (Gorroño et al., 1979). Later on, other fossil bearing levels were found at the southern side of the ravine, located at around -36.5572°N -69.6931°W, 1316m (4,318feet) elevation.[19]
The site is one of five recognized fossiliferous sites in Mendoza Province, with Divisadero Largo, where the Santacrucian Mariño Formarion is found, Huaquerías, defining the Huayquerian in the Huayquerías Formation, the Aisol Formation of central Mendoza and the Uspallata Group and Carrizal Formations in the north of the province.[25]
The geological characterization and the preliminary faunal list were published by Gorroño et al. (1979). The faunal assemblage was then assigned to the Late Oligocene (Deseadan SALMA) based on the presence of two typical representatives of the Deseadean fauna of Patagonia; Pyrotherium and Proborhyaena gigantea,[19] both also found in the Puesto Almendra member of the Sarmiento Formation.[26]
The species epithet Mendozahippus fierensis and genus Fieratherium refer to Quebrada Fiera.[24] [27] [28] [29]
The formation has provided fossils of:[2]
Group | Clade | Taxa | Site | Images | Notes |
---|---|---|---|---|---|
Ungulates | Coniopternium andinum | Quebrada Fiera North | |||
cf. Lambdaconus suinus | Quebrada Fiera North | ||||
Pyrotherium romeroi | Quebrada Fiera North | ||||
Pyrotherium sp. | Quebrada Fiera South | ||||
Litopterna indet. | Quebrada Fiera North | ||||
Meteutatus aff. lagenaformis | Quebrada Fiera North | ||||
?Prozaedyus aff. impressus | Quebrada Fiera North | ||||
Stenotatus aff. ornatus | Quebrada Fiera North | ||||
Glyptodontinae | Glyptodontinae indet. | Quebrada Fiera North | |||
?Megalonychidae indet. | Quebrada Fiera North | ||||
Mendozahippus fierensis | Quebrada Fiera South | ||||
Quebrada Fiera North | |||||
Notohippidae indet. | Quebrada Fiera North | ||||
cf. Archaeotypotherium sp. | Quebrada Fiera North | ||||
Archaeohyrax suniensis | Quebrada Fiera North | ||||
Prosotherium garzoni | Quebrada Fiera North | ||||
cf. Prosotherium sp. | Quebrada Fiera North | ||||
Prohegetotherium malalhuense | Quebrada Fiera North | ||||
P. schiaffinoi | Quebrada Fiera North | ||||
P. cf. sculptum | Quebrada Fiera North | ||||
Prohegetotherium sp. | Quebrada Fiera North | ||||
Hegetotheriopsis sulcatus | Quebrada Fiera North | ||||
Asmodeus petrasnerus | Quebrada Fiera North | ||||
Argyrohyrax proavus | Quebrada Fiera North | ||||
Progaleopithecus sp. | Quebrada Fiera North | ||||
Interatheriidae indet. | Quebrada Fiera South | ||||
Gualta cuyana | Quebrada Fiera North | ||||
Trachytherus cf. spegazzinianus | Quebrada Fiera North | ||||
Proadinotherium sp. | Quebrada Fiera North | ||||
Toxodontidae indet. | Quebrada Fiera North | ||||
Rodents | Acaremyidae indet. | Quebrada Fiera North | |||
Pharsophorus sp. | Quebrada Fiera North | ||||
Proborhyaena gigantea | Quebrada Fiera North | ||||
Fieratherium sorex | Quebrada Fiera North | ||||
Birds | cf. Andrewsornis sp. | Quebrada Fiera North | |||
Quebrada Fiera South | |||||
Invertebrates | Gastropods | Gastropoda indet. | Quebrada Fiera North | ||
See main article: Deseadan and South American land mammal age. The Deseadan South American land mammal age (SALMA) is equivalent to the Arikareean in the North American land mammal age (NALMA) and the Harrisonian in the 2000 version of the classification. It overlaps with the Hsandagolian of Asia and the MP 25 zone of Europe, the Waitakian and the Landon epoch of New Zealand.
Formation | Map | |||||||||||||||||||||||||||
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Basin | align=center rowspan=17 | |||||||||||||||||||||||||||
Archaeohyrax | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | ||||||||||||||||
Prohegetotherium | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
Pyrotherium | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
Pharsophorus | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
Trachytherus | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | ||||||||||||||||
Proadinotherium | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
Proborhyaena | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
Meteutatus | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
Andrewsornis | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
Terror birds | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | ||||||||||||||
Rodents | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | ||||||||||||||
Reptiles | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | ||||||||||||||
align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | |||||||||||||||
Insects | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | align=center | ||||||||||||||
Alluvial | Fluvial | Eolian Alluvial-fluvial | Fluvial | Alluvial | Fluvial-alluvial | Fluvial | Fluvio-lacustrine | Alluvial-fluvial | Lacustrine | Fluvial | ||||||||||||||||||
Volcanic | Yes | Yes | Yes | Yes | Yes | Yes | ||||||||||||||||||||||