scholarly journals Eustatic and tectonic change effects in the reversion of the transcontinental Amazon River drainage system

2016 ◽  
Vol 46 (2) ◽  
pp. 301-328 ◽  
Author(s):  
Mario Vicente Caputo ◽  
Emilio Alberto Amaral Soares

ABSTRACT: The development of the transcontinental Amazon River System involved geological events in the Andes Chain; Vaupés, Purus and Gurupá arches; sedimentary basins of the region and sea level changes. The origin and age of this river have been discussed for decades, and many ideas have been proposed, including those pertaining to it having originated in the Holocene, Pleistocene, Pliocene, Late Miocene, or even earlier times. Under this context, the geology of the sedimentary basins of northern Brazil has been analyzed from the Mesozoic time on, and some clarifications are placed on its stratigraphy. Vaupés Arch, in Colombia, was uplifted together with the Andean Mountains in the Middle Miocene time. In the Cenozoic Era, the Purus Arch has not blocked this drainage system westward to marine basins of Western South America or eastward to the Atlantic Ocean. Also the Gurupá Arch remained high up to the end of Middle Miocene, directing this drainage system westward. With the late subsidence and breaching of the Gurupá Arch and a major fall in sea level, at the beginning of the Late Miocene, the Amazon River quickly opened its pathway to the west, from the Marajó Basin, through deep headward erosion, capturing a vast drainage network from cratonic and Andean areas, which had previously been diverted towards the Caribbean Sea. During this time, the large siliciclastic influx to the Amazon Mouth (Foz do Amazonas) Basin and its fan increased, due to erosion of large tracts of South America, linking the Amazon drainage network to that of the Marajó Basin. This extensive exposure originated the Late Miocene (Tortonian) unconformity, which marks the onset of the transcontinental Amazon River flowing into the Atlantic Ocean.

2009 ◽  
Vol 49 (1) ◽  
pp. 337 ◽  
Author(s):  
Georgina Ryan ◽  
George Bernardel ◽  
John Kennard ◽  
Andrew T Jones ◽  
Graham Logan ◽  
...  

Numerous Miocene reefs and related carbonate build-ups have been identified in the Rowley Shoals region of the central North West Shelf, offshore Western Australia. The reefs form part of an extensive Miocene reef tract over 1,600 km long, which extended northward into the Browse and Bonaparte basins and southward to North West Cape in the Carnarvon Basin—comparable in length to the modern Great Barrier Reef. Growth of the vast majority of these Miocene reefs failed to keep pace with relative sea-level changes in the latest Miocene, whereas reef growth continued on the central North West Shelf to form the three present-day atolls of the Rowley Shoals: Mermaid, Clerke and Imperieuse reefs. In the Rowley Shoals region, scattered small build-ups and local reef complexes were first established in the Early Miocene, but these build-ups were subsequently terminated at a major Mid Miocene sequence boundary. Widespread buildups and atoll reefs were re-established in the Middle Miocene, and the internal stacking geometries of the reefs appear to relate to distinct growth phases that are correlated with eustatic sea-level fluctuations. These geometries include: a basal aggradational buildup of early Middle Miocene age; a strongly progradational growth phase in the late Middle to early Late Miocene that constructed large reef atolls with infilling lagoon deposits; and a back-stepped aggradational growth phase that formed smaller reef caps in the early–latest Late Miocene. Growth of the majority of the reefs ceased at a major sea-level fall in the Late Miocene (Messinian), and only the reefs of the present-day Rowley Shoals (Mermaid, Clerke and Imperieuse reefs, as well as a drowned shoal to the southwest of Imperieuse Reef) continued to grow after this event. Growth of the Rowley Shoals reefs continued to keep pace with Pliocene-Recent sea-level changes, whereas the surrounding shelf subsided to depths of 230–440 m. We conclude that initial reef growth in the Rowley Shoals region was controlled by transpressional reactivation and structuring of the Mermaid Fault Zone during the early stage of collision between the Australian and Eurasian plates. During this structural reactivation, seabed fault scarps and topographic highs likely provided ideal sites for the initiation of reef growth. The subsequent growth and selective demise of the reefs was controlled by the interplay of eustatic sea-level variations and differential subsidence resulting from continued structural reactivation of the Mermaid Fault Zone. In contrast to models proposed in other regions, there is no direct evidence that active or palaeo hydrocarbon seepage triggered or controlled growth of the Rowley Shoals reefs or their buried Miocene predecessors.


1988 ◽  
Vol 62 (3) ◽  
pp. 463-467 ◽  
Author(s):  
Villarroel A. Carlos ◽  
Larry G. Marshall

A new argyrolagoid marsupial, Hondalagus altiplanensis n. gen., n. sp., from the middle Miocene (Santacrucian–Friasian) age locality of Quebrada Honda in southernmost Bolivia represents the smallest and most specialized member of the family Argyrolagidae known. The lower molars are hypselodont and lack vertical grooves labially and lingually, and M4 is greatly reduced relative to M3. In overall size and structure, H. altiplanensis compares best with Microtragulus catamarcensis (Kraglievich, 1931) from rocks of late Miocene (Huayquerian) age in northwest Argentina. Hondalagus altiplanensis demonstrates that the adaptive radiation of argyrolagoids was much greater than previously envisioned, and that generic differentiation of known taxa occurred no later than early–middle Miocene time in South America.


Clay Minerals ◽  
1993 ◽  
Vol 28 (1) ◽  
pp. 61-84 ◽  
Author(s):  
M. Thiry ◽  
T. Jacquin

AbstractThe distribution of clay minerals from the N and S Atlantic Cretaceous deep-sea sediments is related to rifting, sea-floor spreading, sea-level variations and paleoceanography. Four main clay mineral suites were identified: two are inherited and indicative of ocean geodynamics, whereas the others result from transformation and authigenesis and are diagnostic of Cretaceous oceanic depositional environments. Illite and chlorite, together with interstratified illite-smectite and smectite occur above the sea-floor basalts and illustrate the contribution of volcanoclastic materials of basaltic origin to the sediments. Kaolinite, with variable amounts of illite, chlorite, smectite and interstratified minerals, indicates detrital inputs from continents near the platform margins. Kaolinite decreases upward in the series due to open marine environments and basin deepening. It may increase in volume during specific time intervals corresponding to periods of falling sea-level during which overall facies regression and erosion of the surrounding platforms occurred. Smectite is the most abundant clay mineral in the Cretaceous deep-sea sediments. Smectite-rich deposits correlate with periods of relatively low sedimentation rates. As paleoweathering profiles and basal deposits at the bottom of Cretaceous transgressive formations are mostly kaolinitic, smectite cannot have been inherited from the continents. Smectite is therefore believed to have formed in the ocean by transformation and recrystallization of detrital materials during early diagenesis. Because of the slow rate of silicate reactions, transformation of clay minerals requires a long residence time of the particles at the water/sediment interface; this explains the relationships between the observed increases in smectite with long-term sea-level rises that tend to starve the basinal settings of sedimentation. Palygorskite, along with dolomite, is relatively common in the N and S Atlantic Cretaceous sediments. It is not detrital because correlative shelf deposits are devoid of palygorskite. Palygorskite is diagnostic of Mg-rich environments and is indicative of the warm and hypersaline bottom waters of the Cretaceous Atlantic ocean.


2020 ◽  
Vol 51 (1) ◽  
pp. 131-145 ◽  
Author(s):  
P. Maurizot ◽  
J. Collot ◽  
D. Cluzel ◽  
M. Patriat

AbstractThe Loyalty Ridge lies to the east and NE of the Norfolk Ridge. The three main Loyalty Islands (Maré, Lifou and Ouvéa) emerge from the ridge at the same latitude as Grande Terre. The islands are uniformly composed of carbonate deposits, except for Maré, where Middle Miocene intra-plate basalts and associated volcaniclastic rocks form restricted outcrops. Miocene rhodolith limestones constitute the bulk of the carbonate cover of the three islands. On Maré, these platform accumulations are locally topped by a dolomitic hardground, which, in turn, is covered by Pliocene–Pleistocene coral-bearing formations. These coral reef constructions are preserved as elevated rims over all three islands and define an atoll stage in their development. The Pleistocene–Holocene palaeoshoreline indicators include fringing bioconstructions and marine notches and record both eustatic sea-level changes and tectonic deformation. The ridge has been in the forebulge region in front of the active Vanuatu subduction zone since the Pliocene and each of the three islands has been uplifted and tilted to varying degrees. Offshore, the Loyalty Ridge continues northwards to the d'Entrecasteaux Zone and southwards to the Three Kings Ridge. Although typically volcanic, the nature of the deep Loyalty Ridge remains unknown.


2020 ◽  
Vol 90 (8) ◽  
pp. 938-968
Author(s):  
Ariana Osman ◽  
Ronald J. Steel ◽  
Ryan Ramsook ◽  
Cornel Olariu ◽  
Si Chen

ABSTRACT Icehouse continental-shelf-margin accretion is typically driven by high-sediment-supply deltas and repeated glacio-eustatic, climate-driven sea-level changes on a ca. 100 ky time scale. The paleo–Orinoco margin is no exception to this, as the paleo–Orinoco River Delta with its high sediment load prograded across Venezuela, then into the Southern and Columbus basins of Trinidad since the late Miocene, depositing a continental-margin sedimentary prism that is > 12 km thick, 200 km wide, and 500 km along dip. The Cruse Formation (> 800 m thick; 3 My duration) records the first arrival of the paleo–Orinoco Delta into the Trinidad area. It then accreted eastwards, outwards onto the Atlantic margin, by shallow to deepwater clinoform increments since the late Miocene and is capped by a major, thick flooding interval (the Lower Forest Clay). Previous research has provided an understanding of the paleo–Orinoco Delta depositional system at seismic and outcrop scales, but a clinoform framework detailing proximal to distal reaches through the main fairway of the Southern Basin has never been built. We integrate data from 58 wells and outcrop observations to present a 3-D illustration of 15 mapped Cruse clinoforms, in order to understand the changing character of the first Orinoco clastic wedge on Trinidad. The clinoforms have an undecompacted average height of 550 m, estimated continental slope of 2.5° tapering to 1°, and a distance from shelf edge to near-base of slope of > 10 km. The clinoform framework shows trajectory changes from strong shelf-margin progradation (C10–C13) to aggradation (C14–C20) and to renewed progradation (C21–24). Cruse margin progradational phases illustrate oblique clinothem geometries that lack well-developed topsets but contain up to 70 m (200 ft) thick, deepwater slope channels. This suggests a high supply of sediment during periods of repeated icehouse rise and fall of eustatic sea level, with fall outpacing subsidence rates at times, and delivery of sand to the deepwater region of the embryonic Columbus channel region. Also, evidence of wholesale shelf-edge collapse and canyon features seen in outcrop strongly suggest that deepwater conduits for sediment dispersal and bypass surfaces for Cruse basin-floor fans do exist. The change to a topset aggradational pattern with a rising shelf trajectory may be linked to increased subsidence associated with eastward migration of the Caribbean plate. The Cruse-margin topsets were dominated by mixed fluvial–wave delta lobes that were effective in delivery of sands to the basin floor. The preservation of a fluvial regime of the delta may have been impacted by basin geometry which partly sheltered the area from the open Atlantic wave energy at the shelf edge. Ultimately, understanding shelf-edge migration style as well as process-regime changes during cross-shelf transits of the delta will help to predict the location of bypassed sands and their delivery to deepwater areas.


2021 ◽  
Vol 69 (Suppl.1) ◽  
pp. 35-50
Author(s):  
Claudia-J. Del Río ◽  
Sergio Martínez

Introduction: Scutelliforms were diverse and widespread in shallow marine environments during Neogene times in South America. Nevertheless, they have almost never been used as biostratigraphic tools. Objective: To provide a refined stratigraphic frame useful for calibrating temporal dimensions of scutelliform diversity from Argentina and Uruguay and its correlation with the molluscan assemblages previously proposed. Methods: A detailed survey of their geographic and stratigraphic provenance was carried out. We revised both the bibliography and collections (institutional and from our own field work). Results: The group is represented by 14 species belonging to six genera, and four assemblages were identified. Numerical dates of the Neogene marine rocks obtained recently allowed their placement in a chronological scheme: “Iheringiella” sp. A is restricted to the late Oligocene, the genera Camachoaster and “Eoscutella” and the species Monophoraster telfordi to the early Miocene, Abertella gualichensis and Abertella miskellyi to the middle Miocene, and Monophoraster duboisi, Amplaster coloniensis and Amplaster ellipticus to the late Miocene. Non-lunulate scutelliforms are not restricted to the late Oligocene as previously supposed. The oldest occurrence of the genus Monophoraster corresponds to the early Miocene, and along with Iheringiella are long-living taxa that embrace the 25.3 Ma-18.1 Ma (Iheringiella patagonensis) and approximately 15 Ma-6.48 Ma (Monophoraster darwini) intervals. The presence of Iheringiella in the early Miocene of northeastern Patagonia is corroborated, reaching there its northernmost distribution. Monophoraster darwini has a temporal range from the late Miocene (where it was previously thought to be restricted) back to the middle Miocene, since this is the species yielded in the well-known and discussed “Monophoraster and Venericor Beds”. Conclusions: The Paleogene-Neogene scutelliforms of Argentina and Uruguay range from the late Oligocene to the late Miocene. There is a good correspondence among the numerical ages, molluscan biozones and scutelliform assemblages.


2021 ◽  
pp. 1-21
Author(s):  
Daniel Lima ◽  
Orangel Aguilera ◽  
Marcos Tavares

Abstract The spider crabs Willinachoides santanai n. gen. n. sp. from the early-middle Miocene of north Brazil and Paradasygyius rodriguezi n. sp. from the late Miocene of Venezuela are described and illustrated. Additionally, Eoinachoides senni Van Straelen, 1933, from the late Oligocene–early Miocene of Venezuela, is redescribed based on photographs of the holotype, and the diagnosis of Eoinachoides latispinosus Carriol, Muizon, and Secretan, 1987, from the late Miocene of Peru, is emended also on the basis of photographs of the holotype. The past distribution points to a Tethyan background for the current amphi-American Inachoididae, with the oldest fossil species known from the early Eocene Tethyan regions (Pakistan and Italy), and from the late Eocene–late Pliocene of the Americas. The high number of monotypic genera in Inachoididae could be the result of rapid dispersion followed by diversification during the Neogene of the tropical America, facilitated by global and regional events (e.g., eustatic sea level changes, the Mi-1 Oligocene-Miocene boundary global cooling, the global warming period of the Middle Miocene Climate maximum, closure of the Panama Isthmus, and marine incursions into the Amazon Basin). The shoaling and final closure of the Central American Seaway are thought to have critically affected the evolution of the inachoidids and shaped their current distribution patterns. UUID: http://zoobank.org/6275fdc4-4bfa-4873-9320-3143d4915172.


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