Thomas J. DeVries’s research while affiliated with Burke Museum of Natural History and Culture and other places

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Publications (34)


Chronology and Paleoenvironment of the Tunga Formation, a new lowermost Miocene sequence in the East Pisco Basin of southern Peru
  • Article

September 2024

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49 Reads

Stratigraphy

Thomas J. DeVries

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The East Pisco Basin, occupying the coastal plain of Peru between 13°S and 16°S, is widely known for its extensive Eocene to Quaternary biosiliceous deposits and excellent preservation of fossil marine vertebrates. Biochronologic studies published over the past 35 years record a hiatus of about 13 million years (*32–19 Ma) separating the youngest Paleogene deposits (Otuma Formation) from the oldest Neogene deposits (Chilcatay Formation). We describe a newly identified Lower Miocene depositional sequence that lies below documented Chilcatay strata, rich in diatoms and benthic foraminifers, which we name the Tunga Formation. A low-latitude diatom assemblage from the Tunga Formation indicates an age of 21.6 to 20.5 Ma age, whereas an ash within basal Tunga strata yields an 206Pb/238U weighted mean age of 20.58 ± 0.13 Ma. Benthic foraminifer paleodepth analysis and the diatom assemblage of the Tunga Formation indicate deposition took place along the continental margin at upper bathyal depths under hypoxic conditions beneath highly productive waters, a scenario also supported by the presence of abundant clupeoid fish scales and dolomitized horizons. The Tunga Formation is characterized by a profound scarcity of cetacean fossils, unlike the cetacean-rich neritic sediments of the overlying Chilcatay Formation.


Chronology and Paleoenvironment of the Tunga Formation, a new lowermost Miocene sequence in the East Pisco Basin of southern Peru

September 2024

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81 Reads

Stratigraphy

The East Pisco Basin, occupying the coastal plain of Peru between 13°S and 16°S, is widely known for its extensive Eocene to Quaternary biosiliceous deposits and excellent preservation of fossil marine vertebrates. Biochronologic studies published over the past 35 years record a hiatus of about 13 million years (*32-19 Ma) separating the youngest Paleogene deposits (Otuma Formation) from the oldest Neogene deposits (Chilcatay Formation). We describe a newly identified Lower Miocene depositional sequence that lies below documented Chilcatay strata, rich in diatoms and benthic foraminifers, which we name the Tunga Formation. A low-latitude diatom assemblage from the Tunga Formation indicates an age of 21.6 to 20.5 Ma age, whereas an ash within basal Tunga strata yields an 206 Pb/ 238 U weighted mean age of 20.58 ± 0.13 Ma. Benthic foraminifer paleodepth analysis and the diatom assemblage of the Tunga Formation indicate deposition took place along the continental margin at upper bathyal depths under hypoxic conditions beneath highly productive waters, a scenario also supported by the presence of abundant clupeoid fish scales and dolomitized horizons. The Tunga Formation is characterized by a profound scarcity of cetacean fossils, unlike the cetacean-rich neritic sediments of the overlying Chilcatay Formation.


Figure 60. Histogram of diagonal widths of Aulacodiscus lissoni (Douvillé, 1921). Parametric estimation of normal curve based on statistical analysis using software package PAST 4.14b (Hammer et al., 2001).
Figures 2-8. Syntypes of Aulacodiscus lissoni (Douvillé, 1921). 2, 3, 4, 7, 8. UCBL-EM 31733a. Syntype: Ventral, dorsal, left lateral, anterior, and posterior views. L = 29.3 mm. 5, 6. UCBL-EM 31733b. Syntype: Broken, dorsal and left lateral views of juvenile whorls. W = 15.5 mm (Fig. 5).
Figures 9-18. Veatchia carolinae (Maury, 1912). 9-11. PRI 28531. Holotype from Trinidad: Dorsal, ventral, and right lateral views. L = 27 mm. 12, 13. UNCMHN-15076-5798. Specimen from Colombia: Dorsal and ventral views. Drawings from Etayo-Serna (1979). L = ~41 mm. 14-18. MNHN.F.R06288. Specimen from Senegal: Ventral, dorsal, right lateral, left lateral, and posterior views. L = ~36 mm. postC = posterior canal.
Figures 19-29. Shell morphology of Aulacodiscus lissoni (Douvillé, 1921) and Veatchia carolinae (Maury, 1912). 19, 20, 23. A. lissoni, PRI 107870: Ventral and dorsal views and cut-away ventral diagram showing teleoconch whorls and sub-adult periphery. 21. V. carolinae, Senegal, MNHN.F.R06288: Dorsal view. 22. V. carolinae, Colombia, UNCMHN-15076-5798: Dorsal view. 24-26. A. lissoni, juvenile specimens (PRI 107881, L = 19.5 mm; MUSM INV 306, L = 21.5 mm; PRI 107882, L = 21.6 mm): Axial and spiral sculpture and the narrow juvenile aperture. 27, 28. A. lissoni: longitudinally (RGM.1364530) and transversely (NRM Mo 195128) sectioned specimens showing sub-adult periphery. 29. A. lissoni, PRI 107887: Adult with missing dorsal callus revealing underlying juvenile shell and thin dorsal sub-adult callus. ANT = anterior pointed towards viewer, antC = anterior (siphonal) canal, dLLc = dorsal left lateral callus, dRLc = dorsal right lateral callus, POST = posterior pointed away from viewer, postC = posterior canal, postN = posterior notch, subPER = sub-adult periphery, vLLc = ventral left lateral callus, vRLc = ventral right lateral callus, vmS = ventral medial sulcus.
Figures 30-49. Aulacodiscus lissoni (Douvillé, 1921). 30-34, 39. PRI 107870: Ventral, dorsal, left lateral, right lateral, oblique right lateral, and anterior views with rare example of a dorsal predation trace (Fig. 31). L = 33.4 mm, W = 27.1 mm. 35-38, 40, 45. PRI 107871: Ventral, dorsal, left lateral, right lateral, anterior, and posterior views. L = 33.4 mm, W = 27.0 mm. 41-44, 49. PRI 107872: Ventral, dorsal, left lateral, right lateral, and posterior views. L = 32.7 mm, W = 30.8 mm. 46. PRI 107878: Ventral view. L = 24.7 mm. 47, 48. PRI 107875: Posterior, left lateral views. L = 22.2 mm, W = 19.4 mm. predT = predation trace.

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Cookie snails: The Eocene gastropod Aulacodiscus lissoni (Douvillé, 1921) from Peru re-described and compared with other calyptraphorines (Stromboidea: Rostellariidae)
  • Article
  • Full-text available

August 2024

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249 Reads

The Nautilus

The calyptraphorine stromboid, Aulacodiscus lissoni (Douvillé, 1921), found in northern Peru in bioclastic sandstones of the lower Eocene Basal Salina Formation, is notable for its complete envelopment by calluses, including massive left-lateral callus knobs. Previous shell descriptions suffered from the absence of the anterior end. Newly reported specimens reveal an outer lip with a well-formed posterior notch and a short anterior spine, both unique to calyptraphorines. A suite of characters (inter alia, an extended posterior canal, notched outer lip, and dorsal callus knob) indicate A. lissoni burrowed just below the sediment surface in an environment where exhumation and overturning by waves or predators were a constant risk; more than half of the specimens exhibit ventral traces of predation that were likely lethal. The calyptraphorine taxon most similar to A. lissoni, the thickly callused Paleocene Veatchia carolinae (Maury, 1912), inhabited sandy carbonate platforms in Senegal, Trinidad, and Colombia. A calyptraphorine phylogeny that would include both thickly callused species is precluded at present by the scarcity and incompleteness of specimens of V. carolinae and the geographically and temporally isolated occurrence of A. lissoni in the eastern Pacific Ocean.

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Map of the main South American Biogeographic marine areas. Modified from Miloslavish et al. (2011).
Some representative molluscan species of the Peruvian Province. 1. Argopecten purpuratus (13.89° S, 76.31° W); 2. Aulacomya atra (12.07° S, 77.16° W); 3. Trachycardium procerum (13.89° S, 76.31° W); 4. Mesodesma donacium (12.83° S, 76.54° W); 5. Concholepas concholepas (13.89° S, 76.31° W); 6. Thaisella chocolata (13.89° S, 76.31° W); 7. Fissurella peruviana (12.82° S, 76.55° W); 8. Semele solida (13.89° S, 76.31° W); 9. Tagelus dombeii (5.49° S, 81° W); 10. Mulinia edulis (17.42° S, 71.2° W); 11. Prunum curtum (13.89° S, 76.31° W). All specimens are housed at the Collection of Modern and Fossil Mollusks of the Peruvian Littoral, gathered by Luc Ortlieb and kept at the Universidad Peruana Cayetano Heredia (UPCH).
The temperate marine Peruvian Province: How history accounts for its unusual biota

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Thomas J. DeVries

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Miguel Griffin

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The Peruvian Province, from 6° S in Peru to 42° S in Chile, is a highly productive coastal marine region whose biology and fossil record have long been studied separately but never integrated. To understand how past events and conditions affected today's species composition and interactions, we examined the role of extinction, colonization, geologic changes to explain previously unrecognized peculiar features of the biota and to compare the Peruvian Province's history to that of other climatically similar temperate coasts. We synthesized all available data on the benthic (or benthically feeding) biota, with emphasis on fossilizable taxa, for the interval from the Miocene (23–5.4 Ma) and Pliocene (5.4–2.5 Ma) to the present. We outline the history of ecological guilds including primary producers, herbivores, predators, and suspension‐feeders and document patterns of extinction, colonization, and geographic restriction. We identify twelve unusual attributes of the biota, most of which are the result of repeated episodes of extinction. Several guilds present during the Miocene and Pliocene are not represented in the province today, while groups such as kelps and perhaps intertidal predatory sea stars are relative newcomers. Guilds on soft bottoms and in sheltered habitats were severely affected by extinction, whereas those on hard bottoms were most affected by colonists and held their own in diversity. The Peruvian Province has not served as a biogeographic refuge, in contrast to the coasts of Australasia and Argentina, where lineages no longer present in the Peruvian Province survive. The loss of sheltered habitats since the Pliocene explains many of the present‐day peculiarities of the biota. The history of the province's biota explains its unique attributes. High productivity, a rich Southern Hemisphere heritage, and colonization from the north account for the present‐day composition and unusual characteristics of the biota.


Double-phased controlled and influenced biomineralization in marine invertebrates: The example of Miocene to recent reef-building polychaete cirratulids from southern Peru

April 2024

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251 Reads

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1 Citation

Palaeogeography Palaeoclimatology Palaeoecology

Carbonate biomineralization normally occurs in three distinct types: controlled, induced and influenced, each with its peculiar characteristics. Building-reef species within the family Cirratulidae (Annelida, Polychaeta) constitute the first known example of “double-phased” biomineralization among marine invertebrates, as they combine controlled and influenced biomineralization types in the process of developing carbonate tube aggregates. The ultrastructure of the tubes, composed of thin calcareous lamellae with a spherulitic prismatic ultrastructure, as well as lamellae with a homogeneous structure, is produced directly by the worms living inside them and clearly indicates a controlled biomineralization, while the calcareous matrix with agglutinated xenolithic granules that fills the areas between the tubes of the same aggregate is the product of an influenced biomineralization. The reason why this biomineralization process occurs is yet unknown. This study is therefore aimed at describing in detail for the first time the biomineralization of Miocene (Diplochaetetes) and Recent (Dodecaceria) tubes of cirratulid aggregates from southern Peru via optical microscopy, epifluorescence, SEM and EDS analyses. Furthermore, a detailed morphometric and compositional study of tubes was performed and results were statistically evaluated. The comparison with recent cirratulids allowed the recognition of the double-phased biomineralized skeletons in the fossil specimens, despite the different degree of recrystallization which affected the studied Peruvian bioconstructions. This observation suggests that this type of biomineralization has not changed over the course of the entire Cenozoic and can be considered a unique evolutionary character which probably was developed by these polychaetes to be safer from predators, as well as generally more stable and more resistant to environmental stressing factors.



The Miocene stratigraphy of the Laberinto area (Río Ica Valley) and its bearing on the geological history of the East Pisco Basin (south-central Peru)

August 2021

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112 Reads

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20 Citations

Journal of South American Earth Sciences

Global sea-level changes and substantial vertical displacement along the Monte Grande Fault (MGF) in the lower Río Ica Valley of south-central Peru influenced the accumulation of bioclast-bearing and diatom-bearing Miocene siliciclastic sediments in an area of the East Pisco forearc basin (EPB) colloquially known as Laberinto. Two depositional hiatuses in the Laberinto area (~17–14 Ma, ~12.5–10 Ma) manifest as sediment-filled erosional depressions a few kilometers in breadth. Erosion of the older depression was preceded by an ~18-Ma massive debris flow, possibly triggered by motion on the MGF causing lower Miocene lithoclastic olistoliths of up to two hundred meters length to spill off the footwall block. Sediment shed from the same footwall block may have formed previously recognized early Miocene deltas. From 14–13 Ma, the older depression filled with sediments herein assigned to the provisionally named Laberinto, Pampa, and Naranja members of the Pisco Formation, the latter member being characterized by marine delta foreset beds. The three members are at least partly correlative with the Pisco-0 sequence of the Pisco Formation. The younger depression was overrun at 10 Ma by debris flows of lithoclastic and granitic cobbles and boulders, then filled with diatomaceous silty sand with five-meter-sized lithoclastic olistoliths. The two lithologies constitute the provisionally named Mature Formation. Radiometric and newly revised biochronological data from throughout the EPB coupled with new diatom data from the Laberinto area have provided new insights into the correlation of sequences within the Chilcatay and Pisco formations and the interaction of local and basin-wide tectonism and global eustatic sea-level events across the basin.


Late Neogene evolution of the Peruvian margin and its ecosystems: a synthesis from the Sacaco record

March 2021

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1,159 Reads

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26 Citations

International Journal of Earth Sciences

The highly productive waters of the Humboldt Current System (HCS) host a particular temperate ecosystem within the tropics, whose history is still largely unknown. The Pisco Formation, deposited during Mio-Pliocene times in the Peruvian continental margin has yielded an outstanding collection of coastal-marine fossils, providing an opportunity to understand the genesis of the HCS ecosystem. We present a comprehensive review, completed with new results, that integrates geological and paleontological data from the last 10 My, especially focusing on the southern East Pisco Basin (Sacaco area). We discuss the depositional settings of the Pisco Formation and integrate new U/Pb radiometric ages into the chronostratigraphic framework of the Sacaco sub-basin. The last preserved Pisco sediments at Sacaco were deposited ~ 4.5 Ma, while the overlying Caracoles Formation accumulated from ~ 2.7 Ma onwards. We identified a Pliocene angular unconformity encompassing 1.7 My between these formations, associated with a regional phase of uplift. Local and regional paleoenvironmental indicators suggest that shallow settings influenced by the offshore upwelling of ventilated and warm waters prevailed until the early Pliocene. We present an extensive synthesis of the late Miocene–Pleistocene vertebrate fossil record, which allows for an ecological characterization of the coastal-marine communities, an assessment of biodiversity trends, and changes in coastal-marine lineages in relation to modern HCS faunas. Our synthesis shows that: (i) typical endemic coastal Pisco vertebrates persisted up to ~ 4.5 Ma, (ii) first modern HCS toothed cetaceans appear at ~ 7–6 Ma, coinciding with a decline in genus diversity, and (iii) a vertebrate community closer to the current HCS was only reached after 2.7 Ma. The genesis of the Peruvian coastal ecosystem seems to be driven by a combination of stepwise transformations of the coastal geomorphology related to local tectonic pulses and by a global cooling trend leading to the modern oceanic circulation system.


A new barnacle (Cirripedia: Neobalanoformes) from the early Miocene of Peru: Palaeoecological and palaeobiogeographical implications

June 2019

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146 Reads

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11 Citations

Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen

A new megabalanine barnacle, Austromegabalanus carrioli sp. nov., is described from lower Miocene strata of the Chilcatay Formation (East Pisco Basin, southern Peru). An assessment of the value of interlaminate figures in distinguishing species within the tribe Austromegabalanini from thin sections is provided-a useful identification tool with fossil taxa such as the austromegabalanines, which are commonly found only as fragmented shells. The paper concludes with a reassessment of the palaeobiogeography and distribution patterns of the austromegabalanines, proposing a circum-equatorial origin for this tribe.


Early Paleogene brackish-water molluscs from the Caballas Formation of the East Pisco Basin (Southern Peru)

December 2018

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118 Reads

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9 Citations

Shell beds from the Caballas Formation in the East Pisco Basin of southern Peru have yielded an assemblage of molluscs numerically dominated by oysters and cerithioid and eulimid gastropods, with lesser numbers of neritid, ampullinid, and pyramidelloid gastropods and noetiid, mytilid, anomiid, and cardiid bivalves. The shell beds mark a transition from continental to marine-influenced environments. Palaeontological evidence, including plant twig moulds on the attachment scars of oysters and a high diversity of potamidid gastropods, is consistent with an interpretation of a brackish-water setting. The majority of molluscan species from the Caballas Formation show a close affinity with Late Cretaceous species from northern Peru, but no unequivocally Cretaceous invertebrate taxa (e.g. ammonites, rudists) have been found. A morphologically distinctive bivalve species that occurs in the Caballas Formation, Carolia (Parinomya) parinensis, only occurs elsewhere in the upper lower Eocene Pariñas and Chacra formations of the Talara Basin of northern Peru. Moreover, several other Caballas Formation molluscan taxa closely resemble early Eocene species from the Talara Basin. These equivocal biostratigraphic data indicate an early Paleogene age as most likely for the Caballas Formation. http://www.zoobnk.org/urn:lsid:zoobank.org:author:25E21A31-0230-48C7-A2ED-A48A98A3F231


Citations (24)


... Successive marine transgressions since the early Eocene have produced several unconformity-bound depositional sequences in the EPB that are now subaerially exposed (DeVries 1998;DeVries and Jud 2018;DeVries et al. 2017;Di Celma et al. 2017;. This Cenozoic infilling has been understood to consist of two extended periods of marine depositionabout 43-32 Ma, principally the Paracas and Otuma formations, and about 19-2 Ma, principally the Chilcatay, Pisco and Caracoles formationswith a hiatus encompassing most of the Oligocene and the earliest Miocene (Bosio et al. 2020;DeVries 1998;DeVries and Jud 2018;DeVries et al. 2021;Di Celma et al. 2017;; textfigure 2). ...

Reference:

Chronology and Paleoenvironment of the Tunga Formation, a new lowermost Miocene sequence in the East Pisco Basin of southern Peru
The Miocene stratigraphy of the Laberinto area (Río Ica Valley) and its bearing on the geological history of the East Pisco Basin (south-central Peru)
  • Citing Article
  • August 2021

Journal of South American Earth Sciences

... This period also coincides with the opening of the Trujillo and Yaquina extensional basins in the FBS. Such pre-Neogene extensional tectonics was described in most of the Peruvian forearc (Genge et al., 2020;Ochoa et al., 2021;Di Celma et al., 2022). The Trujillo Basin and the near-sea level Calipuy Basin were separated by the PH relieves as shown by detrital zircon provenance analysis in the upper Eocene sedimentary rocks of the Calipuy Basin (see section 2.2.6.). ...

Late Neogene evolution of the Peruvian margin and its ecosystems: a synthesis from the Sacaco record

International Journal of Earth Sciences

... The East Pisco Basin is comprised of a larger onshore portion and a smaller submerged part; it is separated from the more seaward West Pisco Basin by an NW-trending alignment of basement elevations known as the Outer Shelf High (Thornburg and Kulm, 1981;Di Celma et al., 2022). The onshore part of the East Pisco Basin is home to one of the most renowned Cenozoic marine Fossil-Lagerstätte whose fossil content includes both vertebrates (e.g., Clarke et al., 2010;Lambert et al., 2010Lambert et al., , 2017Lambert et al., , 2019Esperante et al., 2015;Gioncada et al., 2016;Marx et al., 2017;Bianucci et al., 2018bBianucci et al., , 2023Collareta et al., 2021;Bosio et al., 2021b;Bianucci and Collareta, 2022) and invertebrates (e.g., DeVries, 1988DeVries, , 2007DeVries, , 2016DeVries and Frassinetti, 2003;Coletti et al., 2019;Collareta et al., 2019Collareta et al., , 2023Bosio et al., 2021a;Kočí et al., 2021;Sanfilippo et al., 2021). ...

A new barnacle (Cirripedia: Neobalanoformes) from the early Miocene of Peru: Palaeoecological and palaeobiogeographical implications
  • Citing Article
  • June 2019

Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen

... Priabonian periods in Peru. Likewise, the Peruvian faunas reported for the Middle Eocene (SEPP-Bartonian) and Late Eocene (SEPP-Priabonian) are related to the tropical and subtropical belts of Tethys (Tethys Realm)(Piccoli & Savazzi, 1983;Lozouet, 2014;Das & Halder, 2018;DeVries, 2019). This is con rmed by the number of genera and species of molluscs reported in our study(Fig. ...

Early Paleogene brackish-water molluscs from the Caballas Formation of the East Pisco Basin (Southern Peru)
  • Citing Article
  • December 2018

... Se extiende en la costa por más de 325 km entre las ciudades de Pisco, Ica, Nazca, Lomas y Yauca, en las regiones de Ica y Arequipa, en el centro-sur del Perú ( fig. 1 A y B). Se estima que el espesor total de la sección de la formación Pisco es de 640 m (Brand et al., 2003). Se han podido separar hasta nueve localidades fosilíferas, las cuales tienen diferentes edades que abarcan desde el Mioceno medio (11-13 Ma) hasta el Plioceno tardío (2 Ma) (Muizon & DeVries, 1985: 552-553;Muizon et al., 2004: 389;Stucchi, 2007: 369-370). ...

Stratigraphy of the Miocene/Pliocene Pisco Formation in the Pisco Basin, Peru
  • Citing Article
  • January 2003

... Both Loxechinus albus and Tetrapygus niger catch drift algae, but T. niger does so only in aggregations (Dayton, 1985;Vásquez & Buschmann, 1997). DeVries, 2008a;Nielsen et al., 2004), and the largest species of Nacella (N. reicheae, 80 mm) is also the oldest member of the genus, dating from the latest Oligocene of Peru (DeVries, 2008b). ...

Pliocene and Pleistocene Fissurella Bruguiere, 1789 (Gastropoda : Fissurellidae) from southern Peru
  • Citing Article
  • June 2008

Veliger -Berkeley-

... O gênero Equus Linnaeus, 1758 tem a sua primeira ocorrência na localidade de Tarija, Bolívia, (Alberdi & Prado, 1992;Alberdi & Prado, 1995) atribuído por MacFadden et al. (1983) ao Pleistoceno médio (1.0-0.7 Ma AP). De acordo com Alberdi & Prado (1995) (Alberdi & Prado, 1992, 19952004;Prado & Alberdi, 1994;Alberdi & Frassinetti, 2000;Carlini & Tonni, 2000;Martinez, 2004;Salas et al., 2004;Rincón et al., 2006). Ambos os gêneros são extintos no limite Pleistoceno-Holoceno há cerca de 10.000 anos AP (Ficcarelli et al. 2003). ...

Los mamíferos de Quebrada El Jahuay (Arequipa, Perú): Fauna típica del Pleistoceno tardío de la costa peruana

... Stratigraphic correlation between hills in the East Pisco Basin is not well established. To preserve the stratigraphic value of taphonomic observations, all samples were located by measuring their positions relative to prominent lithologic units in each hill (Brand et al., 2003(Brand et al., , 2006 and by GPS measurements differentially corrected to base stations in the Basin. ...

A contribution to the stratigraphy of the miocene/pliocene Pisco Formation, Peru
  • Citing Article
  • September 2006

Journal of Verterbrate Paleontology

... The East Pisco Basin is comprised of a larger onshore portion and a smaller submerged part; it is separated from the more seaward West Pisco Basin by an NW-trending alignment of basement elevations known as the Outer Shelf High (Thornburg and Kulm, 1981;Di Celma et al., 2022). The onshore part of the East Pisco Basin is home to one of the most renowned Cenozoic marine Fossil-Lagerstätte whose fossil content includes both vertebrates (e.g., Clarke et al., 2010;Lambert et al., 2010Lambert et al., , 2017Lambert et al., , 2019Esperante et al., 2015;Gioncada et al., 2016;Marx et al., 2017;Bianucci et al., 2018bBianucci et al., , 2023Collareta et al., 2021;Bosio et al., 2021b;Bianucci and Collareta, 2022) and invertebrates (e.g., DeVries, 1988DeVries, , 2007DeVries, , 2016DeVries and Frassinetti, 2003;Coletti et al., 2019;Collareta et al., 2019Collareta et al., , 2023Bosio et al., 2021a;Kočí et al., 2021;Sanfilippo et al., 2021). ...

Fossil Cenozoic crassatelline bivalves from Peru: New species and generic insights

Acta Palaeontologica Polonica

... The white shark originated at the Messinian-Zanclean boundary (Ehret et al., 2012;Boessenecker, 2011) and, based on its tooth fossil record, became relatively frequent in the Pliocene and Pleistocene marine ecosystems (Cappetta, 1987;Marsili, 2006) suggesting a possible continuity of feeding interaction between this apex predator and cetaceans since ca. 5.3 Ma to the Present. ...

ORIGIN OF THE WHITE SHARK (CARCHARODON), BASED ON RECALIBRATION OF THE LATE NEOGENE, PISCO FORMATION OF PERU
  • Citing Article
  • January 2009

Journal of Verterbrate Paleontology