scholarly journals New suoid fossils (Mammalia, Artiodactyla) from the Miocene of Moghara, Egypt, and Gebel Zelten, Libya: biochronological implications

2021 ◽  
Vol 77 (1) ◽  
pp. 111-125
Author(s):  
Martin Pickford ◽  
Mohamed Abdel Gawad ◽  
Mohamed Hamdan ◽  
Ahmed N. El-Barkooky ◽  
Mohammed H. Al Riaydh
Keyword(s):  
Late Miocene ◽  
Middle Miocene ◽  
Early Miocene ◽  
Geological Museum ◽  
Upper Molar

Some undescribed suoid specimens from early and middle Miocene deposits at Moghara, Egypt, and Gebel Zelten, Libya, are of interest for biochronology. The fossils comprise maxillae and mandibles with incomplete dentitions, which are described and illustrated in detail. Three species of suids and one sanithere occur at Moghara. A huge edentulous suid mandible was collected at Gebel Zelten in 1997 during the Spanish-Libyan Palaeontology Expedition. In January, 2020, additional sanithere fossils were collected from Moghara by a team from Cairo University and the Muséum National d’Histoire Naturelle, Paris. A suid mandible with four teeth collected from Moghara in 1994, and now curated at the Cairo Geological Museum, confirms the presence of the species Libycochoerus massai at the site, previously represented by an isolated upper molar and two canines. A talus previously thought to be from Moghara is now known to have been collected at Wadi Natrun (late Miocene) and thus probably represents a tetraconodont rather than a kubanochoere. The age of the Moghara deposits is estimated to span the period ca. 19.5–16.5 Ma (late early Miocene, Faunal Sets PII–PIIIa) and the Zelten sequence is most likely to span the period ca. 17–14.5 Ma (late early Miocene to basal middle Miocene, Faunal Sets PIIIa–PIIIb).

scholarly journals The distribution of <i>Triebelina raripila</i> and <i>Carinocythereis carinata</i> (Ostracoda) from the Middle Miocene of the Central Paratethys and their palaeogeographic implications

1998 ◽  
Vol 17 (2) ◽  
pp. 125-130 ◽  
Author(s):  
J. Szczechura
Keyword(s):  
Shallow Water ◽  
Late Miocene ◽  
Middle Miocene ◽  
Early Miocene ◽  
Central Paratethys ◽  
Eastern Paratethys ◽  
Main Species ◽  
Late Middle Miocene ◽  
The Mediterranean

Abstract. Late Middle Miocene (Upper Badenian) strata of the Fore-Carpathian Depression of Poland yield a shallow-water ostracod fauna which contains the species Triebelina raripila (G. W. Müller, 1894) and Carinocythereis carinata (Roemer, 1838). The palaeobiogeographic distribution of the two main species suggests, that in the late Middle Miocene, Central Paratethys was still connected to the Mediterranean, although still separated from the Eastern Paratethys and from southeastern Eurasia. The continuous occurrence of Triebelina raripila and Carinocythereis carinata in the Mediterranean basins, from the Early Miocene to Recent, indicates that marine conditions existed throughout, thereby allowing them to survive the Late Miocene salinity crisis.

scholarly journals Diversity and biostratigraphy of the late Oligocene-late Miocene sand dollars (Echinoidea: Scutelliformes) of Argentina and Uruguay

2021 ◽  
Vol 69 (Suppl.1) ◽  
pp. 35-50
Author(s):  
Claudia-J. Del Río ◽  
Sergio Martínez
Keyword(s):  
South America ◽  
Late Miocene ◽  
Middle Miocene ◽  
Field Work ◽  
Early Miocene ◽  
Late Oligocene ◽  
Good Correspondence ◽  
Shallow Marine ◽  
Sand Dollars ◽  
Temporal Dimensions

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.

scholarly journals Revision of the European species of Prosantorhinus (Mammalia, Perissodactyla, Rhinocerotidae)

2017 ◽  
Vol 73 (3-4) ◽  
pp. 236-274
Author(s):  
Kurt Heissig
Keyword(s):  
Type Species ◽  
Western Europe ◽  
Middle Miocene ◽  
Early Miocene ◽  
Distal Limb ◽  
European Species ◽  
Medium Length ◽  
Distal Side ◽  
Upper Molar

t is not size that distinguishes the genus Prosantorhinus from Diaceratherium , but the following characters: a concave dorsal skull profile with upslanting nasals and narrowing on the distal side of the last upper molar. Using these characters, in addition to the type species Prosantorhinus germanicus (), the following species can be added to the genus: Prosantorhinus douvillei () (, .), from the Early and Middle Miocene (MN 3–5) of Western Europe, Prosantorhinus laubei from MN 3 of northern Bohemia, Prosantorhinus aurelianensis () from MN 3–4a of Western Europe, and with some reservation “Rhinoceros” tagicus (), an enigmatic species from the Early Miocene (MN 3) of Portugal, known only by its upper cheek teeth. At the beginning of MN 3 (), the metapodials of Prosantorhinus aurelianensis were considerably more robust than those of the latest Diaceratherium species (Laugnac, MN 2b) (.) Within the genus shortening of the distal limb segments and narrowing of the distal side of M3 increased with time. The metapodials of Prosantorhinus laubei are less robust but of medium length, in contrast to the Middle Miocene (MN 5) Prosantorhinus germanicus in which they are extremely shortened. No transitional species or co-occurrence of Diaceratherium and Prosantorhinus are known.

Tertiary marine molluscan assemblages of eastern Patagonia (Argentina): A biostratigraphic analysis

2004 ◽  
Vol 78 (6) ◽  
pp. 1097-1122 ◽  
Author(s):  
Claudia Julia del Río
Keyword(s):  
Late Miocene ◽  
Middle Miocene ◽  
Late Eocene ◽  
Early Miocene ◽  
Late Oligocene ◽  
Late Paleocene ◽  
Compositional Changes ◽  
Molluscan Species

Pectinids are the most abundant and widely distributed taxa in the Tertiary marine beds of Patagonia. Along with other very common molluscan species, they characterize five assemblages, from oldest to youngest: 1) the Oligocene Panopea sierrana-Parinomya patagonensis Assemblage; 2) the Late Oligocene–Early Miocene Jorgechlamys centralis–Reticulochlamys borjasensis Assemblage; 3) the Early Miocene Reticulochlamys zinsmeisteri–Struthiolarella patagoniensis–Pleuromeris cruzensis Assemblage; 4) the Early Miocene Pseudoportlandia glabra–Antimelatoma quemadensis Assemblage; and 5) the latest Early Miocene–earliest Middle Miocene Nodipecten sp.–Venericor abasolensis–Glycymerita camaronesia Assemblage. A brief analysis of the origin and composition of these Tertiary Patagonian molluscan faunas is provided. Striking compositional changes occurred through time, recorded mainly in the Late Paleocene, Late Eocene, Late Oligocene–Early Miocene, and Late Miocene.

scholarly journals Small early Miocene listriodont suid (Artiodactyla: Mammalia) from Sabuncubeli (Manisa, SW Anatolia), Turkey

2020 ◽  
Vol 76 (2) ◽  
pp. 325-337
Author(s):  
Martin Pickford ◽  
Tanju Kaya ◽  
Erhan Tarhan ◽  
Derya Erylmaz ◽  
Serdar Mayda
Keyword(s):  
Late Miocene ◽  
Middle Miocene ◽  
New Genus ◽  
Morphological Features ◽  
Early Miocene ◽  
New Genus And Species ◽  
The Family

Turkey is known for the wealth of fossil suids found in deposits of middle Miocene, late Miocene and Plio-Pleistocene levels but material of this family from early Miocene and Palaeogene deposits is rare in the country, one of the few published occurrences being from Şemsettin (Kumartaş Formation, MN 4, Çankiri-Çorum Basin). For this reason, it is interesting to record the presence of small suid remains in the Soma Formation at Sabuncubeli (Manisa, SW Anatolia) in deposits correlated to MN 3 (early Miocene) and thus the earliest known Turkish members of the family. The upper and lower teeth are herein attributed to a new genus and species (Prolistriodon smyrnensis) of Listriodontinae because, in a nascent way, they show a suite of derived morphological features such as upper central incisors with apical sulci, and upper molars with lingual precrista, found in listriodonts but not in Kubanochoerinae, Palaeochoerinae, Tetracondontinae, Hyotheriinae, Namachoerinae, Cainochoerinae or Suinae.

Neogene Pectinidae (Bivalvia) of tribe Chlamydini Teppner, 1922 in Patagonia (Argentina):ZygochlamysIhering, 1907 and three new genera

2018 ◽  
Vol 93 (2) ◽  
pp. 312-336 ◽  
Author(s):  
María B. Santelli ◽  
Claudia J. del Río
Keyword(s):  
Late Miocene ◽  
Type Species ◽  
Antarctic Circumpolar Current ◽  
Middle Miocene ◽  
New Genus ◽  
Early Miocene ◽  
New Genera ◽  
Early Pliocene ◽  
Circumpolar Current ◽  
The Antarctic

AbstractZygochlamysIhering, 1907 is revised and three new genera of tribe Chlamydini are named: the monospecific early Miocene generaPixiechlamysnew genus (type species:Pecten quemadensisIhering, 1897) andChokekenian. gen. (type species:Zygochlamys nicolasiMorra, 1985), and the late Miocene–early PlioceneMoirechlamysn. gen., containingPecten actinodesSowerby, 1846 (type species) andChlamys auroraeFeruglio, 1954.Zygochlamysis restricted to includeZ. geminata(Sowerby, 1846) (type species),Z. jorgensisIhering, 1907, andZ. sebastianiMorra, 1985. The present analysis increases the biostratigraphic usefulness of the group and improves taxonomic knowledge of the Neogene molluscan assemblages defined previously for Patagonia.Zygochlamys geminatais confined to the latest Oligocene–early Miocene interval of the Austral Basin of Patagonia (Argentina) and to the early Miocene of Chile,Z. jorgensisis restricted to the early to middle Miocene of the Golfo San Jorge and northern Austral Basins, andMoirechlamysn. gen., the most widespread genus, occurs in the late Miocene–early Pliocene of the Austral, Golfo San Jorge, Valdés, and Colorado basins. All these genera are endemic to southern South America;Zygochlamysis not related to other circumpolar genera such asAustrochlamysJonkers, 2003 orPsychrochlamysJonkers, 2003, rejecting its dispersal in the Antarctic Circumpolar Current, as has been proposed previously.UUID:http://zoobank.org/55d7ea85-5ec5-477a-9ede-5d3d795b75b5

scholarly journals The Karpatian (late early Miocene) flora of the Mecsek area

2020 ◽  
pp. 51-122 ◽  
Author(s):  
Lilla Hably
Keyword(s):  
Late Miocene ◽  
Endemic Species ◽  
Riparian Vegetation ◽  
Middle Miocene ◽  
Vegetation Type ◽  
Early Miocene ◽  
Mean Annual Temperature ◽  
Vegetation Types ◽  
Climate Analysis ◽  
High Diversity

A rich macroflora has been collected from Karpatian (late early Miocene) layers of the Mecsek Mts during recent decades. The bulk of the fossil assemblage consists of leaves and also fruits of angiosperms. Among the more than a hundred taxa, several endemic species were described: Leguminocarpum mecsekense Andreánszky, Ailanthus mecsekensis Hably, Nyssa gyoergyi sp. nov., Nyssa gergoei sp. nov., Nyssa sp. 1, Clematis csabae sp. nov., Gordonia sp. and Carpolithes gergoei Hably et Erdei sp. nov. Many taxa were last recorded in the Carpathian Basin, e.g. Cedrelospermum, Ziziphus. Other taxa appeared in this flora, e.g. Quercus kubinyii, Podocarpium podocarpum, Liquidambar europaea and Populus populina, and later became dominant in the middle Miocene (Sarmatian) floras or even in the late Miocene (Pannonian) floras. Four main vegetation types were determined. The most significant types are subxerophytic vegetation showing high diversity, swamp vegetation, riparian vegetation, and a vegetation type growing in habitats with higher rainfall. Thermophilous flora elements are dominant in the assemblage, although “arctotertiary” species also appear. The floristic character of the flora supports the results of an earlier quantitative climate analysis of the Magyaregregy flora, according to which mean annual temperature was 15.6–16.6°C and coldest-month and warmest-month temperatures were 5–6.2°C and 24.7–27.9°C, respectively. Generally the assemblage presented in this paper extends those climatological findings to the late early Miocene.

Middle Miocene (∼14 Ma) and Late Miocene (∼6 Ma) Paleogeographic Boundary Conditions

2021 ◽  
Author(s):  
Zhilin He ◽  
Zhongshi Zhang ◽  
Zhengtang Guo ◽  
Christopher R. Scotese ◽  
Chenglong Deng
Keyword(s):  
Boundary Conditions ◽  
Late Miocene ◽  
Middle Miocene

Foraminifera Biostratigraphy of Two Wells in Niger Delta

2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Dairo VA
Keyword(s):  
Niger Delta ◽  
Middle Miocene ◽  
Early Miocene ◽  
Orbulina Universa ◽  
Exploratory Wells ◽  
Stratigraphic Range

Biostratigraphic studies of foraminifera were carried out on two exploratory wells drilled in the Eastern Niger Delta to establish the age, biozonation and paleoenvironment of the foraminifera present in the strata penetrated by the wells. A total of 80 ditch cutting samples retrieved at 60ft intervals from AX-1 and AX-2 Wells at the depth of 3,600ft to 6,000ft and 4,200ft to 6500ft. respectively were subjected to micropaleontological analysis which involves picking and identification of the foraminifera present. The resulting data were loaded into the Stratabug software and interpreted. The foraminifera recovered and identified from the two wells are made up of both benthic and planktic species. The marker species, whose stratigraphic range are well established were used to describe the biozonation and these includes Heterostegina sp, Catapsydrax stainforthi, Chiloguembelina victoriana, Orbulina universa/suturalis, Praeorbulina sicana,Buliminella subfusiformis, Nonion centrosulcatum, Catapsydrax dissimilis, Globigerinoides bisphericus and Globigerinoides sicanus. Four biozones of foraminifera made up of N8, N7-N8, N6-N7 and N5-N6 were recognised based on the zonation scheme of Grandstein; with their stratigraphic age ranging from early Miocene to middle Miocene. Furthermore, the environment of deposition prevailing in the Formations penetrated by the two wells are predominantly middle neritic with similarity in their ages as observed from the correlation of the biozones from the two wells

Middle Miocene recovery of Caribbean reef corals: New data from the Tamana Formation, Trinidad

2001 ◽  
Vol 75 (3) ◽  
pp. 513-526 ◽  
Author(s):  
Kenneth G. Johnson
Keyword(s):  
Middle Miocene ◽  
New Records ◽  
Early Miocene ◽  
Early Pleistocene ◽  
Reef Corals ◽  
Rigorous Description ◽  
Caribbean Coral Reef ◽  
The Caribbean ◽  
Stratigraphic Ranges ◽  
Biotic Change

Caribbean coral reef communities were restructured by episodes of accelerated biotic change during the late Oligocene/early Miocene and the late Pliocene/early Pleistocene. However, rigorous description of the effects of rapid biotic change is problematic because preservation and exposure of coral-bearing deposits is not consistent in all stratigraphic intervals. In the Caribbean, early and middle Miocene exposures are more rare than late Miocene and Pliocene exposures. One exception is the late early to early middle Miocene Tamana Formation of Trinidad, and old and new collections from this unit were studied to determine the timing of recovery after the Oligocene/Miocene transition. A total of 41 species of zooxanthellate corals were recovered from the unit, including 21 new records. Within these assemblages, species first occurrences outnumber species last occurrences by a factor of four (31 first occurrences and eight last occurrences). The extension of the stratigraphic ranges of species previously first recorded in Pliocene sediments has reduced an apparent Pliocene pulse of origination, indicating that the Pliocene/Pleistocene transition was largely a result of accelerated extinction against a background of near-constant origination. The fact that few species last occur in the Tamana fauna indicates that the Oligocene/Miocene transition was complete by the end of the early Miocene.

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