scholarly journals The early Miocene flora of Güvem (Central Anatolia, Turkey): a window into early Neogene vegetation and environments in the Eastern Mediterranean

2017 ◽  
Vol 57 (2) ◽  
pp. 237-338 ◽  
Author(s):  
Thomas Denk ◽  
Tuncay H. Güner ◽  
Zlatko Kvaček ◽  
Johannes M. Bouchal

AbstractThe early Burdigalian (MN3) plant assemblage of the Güvem area (northwestern Central Anatolia) is preserved in lacustrine sediments of the Dereköy pyroclastics. Its age is well constrained by radiometric dates of basaltic rocks bracketing the pyroclastics, making the Güvem flora one of the extremely few precisely dated early Miocene floras in the Mediterranean region. The rich assemblage of impression fossils comprises ferns and fern allies (2 species), gymnosperms (12 spp.) and angiosperms (129 spp.).Ilex miodipyrenasp. nov. is described as a new fossil-species. The most diverse families in the assemblage are the Fagaceae with 12 taxa and the Fabaceae with 12 leaf morphotypes and one fruit taxon. Aquatic plants are represented by seven taxa, riparian (including palms) and swamp forest elements by >35 taxa, and lianas by three taxa (Smilaxspp.,Chaneya). The relatively large number of aquatic and riparian/swamp elements is congruent with the rich fish, amphibian and reptile record of the Güvem area. Another characteristic feature of the plant assemblage is the presence of various lobed leaves which show similarities with modern species of different families (e.g.Alangium, various Malvales). Trees and shrubs growing on well-drained soils and forming closed-canopy and open-canopy forests are the most diversified group (>70 taxa). In terms of number of specimens in the collection and based on field observations, by far the most abundant leaf fossils belong to evergreen oaks ofQuercus drymejaandQ. mediterraneaand to various types of foliage that cannot be assigned to a particular extant or extinct genus of Fagaceae. These sclerophyllous trees must have covered vast areas surrounding the wetlands that developed during the early Miocene in the Güvem Basin. Based on a recent reassessment of the ecology and taxonomic affinity of these trees, they are considered to reflect humid temperate climatic conditions but with a brief drier season during the winter months. These forests are more similar to the laurel forests of the southeastern United States and those stretching in a narrow belt south of the Himalayas to eastern central China. The large number of Fabaceae may indicate the presence of warm subtropical environments but this is difficult to assess, as they are known for having wide ecological ranges today and in the past. All in all, a larger part of the plant taxa point to forested vegetation. This is in agreement with previous palynological studies which detected only small amounts of herbaceous and grass pollen. Open patches of vegetation may have been restricted to river banks and to rocky areas in a volcanic landscape. The biogeographic patterns detected for the early Miocene of the Güvem assemblage are manifold; most taxa are widespread Northern Hemispheric elements. A substantial part of the species migrated from Asia into Europe during the (late) Paleogene and reached Anatolia during the early Miocene (Fagus,Paliurus,Chaneya,Ailanthus,Quercus kubinyii,Davallia haidingeri,Acer angustilobum,A. palaeosaccharinum). Fewer taxa may have been in Anatolia before they migrated to Europe (e.g.Nerium,Smilax miohavanensis,Quercus sosnowskyi). Finally, very few taxa are Anatolian endemics (e.g.Ilex miodipyrena).

2012 ◽  
Vol 183 (6) ◽  
pp. 661-681 ◽  
Author(s):  
Zbigniew Szyndlar

Abstract The paper reviews the entire fossil record of the Colubridae coming from the European Early Oligocene (MP21) to late Early Pliocene (MN15) localities. Prior to the end of the Early Miocene, European colubrids were rare and dominated by booid snakes. At the end of the Early Miocene (MN4), the archaic ophidian fauna of Europe was literally flooded by eastern immigrants, principally representatives of the colubroid families Colubridae, Elapidae, and Viperidae. Since then, the Colubridae became a dominant group in snake assemblages, both in Europe and elsewhere. The rich colubrid fauna inhabiting the European continent in the Middle Miocene (MN5 to 7+8) was composed exclusively of extinct species, representing mainly fossil genera, although members of living genera were also quite common. At the beginning of the Late Miocene (MN9), almost all fossil genera became extinct, but living genera were represented exclusively by fossil species. In the late Early Pliocene (MN15), almost all European colubrids were living species. The Late Pliocene (MN16) and Pleistocene colubrid snakes did not differ from those inhabiting Europe today.


2019 ◽  
Vol 75 (2) ◽  
pp. 268-280 ◽  
Author(s):  
Ünal Akkemik ◽  
Nevriye Neslihan Acarca Bayam

Taxodioxylon Hartig, (emended by Gothan 1905) was widely described from the late Oligocene of the European part of Turkey (Thrace) and the early Miocene of greater Turkey, Anatolia.,C,. was also described from the early Miocene of central Anatolia. The purpose of this paper is to present a more detailed extended history of these two genera up to the late Miocene (Tortonian) with new descriptions from the Galatean Volcanic Province in central Turkey. The wood identification showed the presence of two fossil species;,D,et B,and,(G,.) G,. In conclusion, the swamp and lowland warm-temperate forest composition including,and,in the Galatean Volcanic Province, continued from the early Miocene (Burdigalian) to the late Miocene (Tortonian).


2021 ◽  
pp. 1-15
Author(s):  
Juan López-Gappa ◽  
Leandro M. Pérez ◽  
Ana C.S. Almeida ◽  
Débora Iturra ◽  
Dennis P. Gordon ◽  
...  

Abstract Bryozoans with calcified frontal shields formed by the fusion of costae, collectively constituting a spinocyst, are traditionally assigned to the family Cribrilinidae. Today, this family is regarded as nonmonophyletic. In the Argentine Cenozoic, cribrilinids were until recently represented by only two fossil species from the Paleocene of Patagonia. This study describes the first fossil representatives of Jolietina and Parafigularia: J. victoria n. sp. and P. pigafettai n. sp., respectively. A fossil species of Figularia, F. elcanoi n. sp., is also described. The material comes from the early Miocene of the Monte León and Chenque formations (Patagonia, Argentina). For comparison, we also provide redescriptions of the remaining extant species of Jolietina: J. latimarginata (Busk, 1884) and J. pulchra Canu and Bassler, 1928a. The systematic position of some species previously assigned to Figularia is here discussed. Costafigularia n. gen. is erected, with Figularia pulcherrima Tilbrook, Hayward, and Gordon, 2001 as type species. Two species previously assigned to Figularia are here transferred to Costafigularia, resulting in C. jucunda n. comb. and C. tahitiensis n. comb. One species of Figularia is reassigned to Vitrimurella, resulting in V. ampla n. comb. The family Vitrimurellidae is here reassigned to the superfamily Cribrilinoidea. The subgenus Juxtacribrilina is elevated to genus rank. Inferusia is regarded as a subjective synonym of Parafigularia. Parafigularia darwini Moyano, 2011 is synonymized with I. taylori Kuklinski and Barnes, 2009, resulting in Parafigularia taylori n. comb. Morphological data suggest that these genera comprise different lineages, and a discussion on the disparities among cribrilinid (sensu lato) spinocysts is provided. UUID: http://zoobank.org/215957d3-064b-47e2-9090-d0309f6c9cd8


1992 ◽  
Vol 6 ◽  
pp. 107-107
Author(s):  
Timothy J. Gaudin ◽  
William D. Turnbull

The mammalian order Xenarthra (including the living Neotropical armadillos, anteaters, and tree sloths) has figured importantly in recent hypotheses of interordinal relationships among eutherian mammals. It has been suggested that the group shares a common ancestry both with the extant Old World order Pholidota (i.e. the pangolins or scaly-anteaters) and the extinct North American group Palaeanodonta. Furthermore, these three groups have been linked together into a monophyletic Cohort Edentata, which has been hypothesized to represent the sister-group to all other eutherians. This placement of edentates relative to the remainder of Eutheria has been supported in part by a purported difference in the morphology of the stapes in the two groups- edentates possessing a primitive, imperforate/columelliform morphology, other placentals a derived, perforate/stirrup-shaped morphology.A recent study of stapedial morphology among mammals by Novacek and Wyss (1986) suggests that within the Xenarthra itself a perforate stapes is found among armadillos, but that the pilosa in particular (the clade including anteaters and sloths) and the order as a whole are characterized primitively by an imperforate stapes. Our studies of the xenarthran ear region (Patterson et al., in press) have uncovered new ontogenetic and paleontological evidence which contradict the findings of Novacek and Wyss. Among adults of the two extant tree sloth genera, the stapes lacks a stapedial foramen. However, in both genera, this adult imperforate morphology is derived from a perforated juvenile stapes. Novacek and Wyss ignored fossil species in their consideration of the xenarthran stapes. It has long been known that extinct ground sloths of the family Mylodontidae possessed a large stapedial foramen. Unfortunately, until now no stapes were known from the remaining ground sloth families, the Megatheriidae and the Megalonychidae. We have uncovered a complete left stapes of an early Miocene megatheriid ground sloth Eucholoeops ingens. This stapes possesses a well-developed stapedial foramen. We believe that this new paleontological evidence, combined with our information on the ontogeny of the stapes in the living genera, clearly indicates that a perforate stapes is primitive for sloths. Moreover, when we plot distributions of stapedial morphologies of both living and fossil edentates onto a phylogeny of the Edentata, we can demonstrate that the a large stapedial foramen is primitive for the Xenarthra as a whole, and probably for the entire Cohort Edentata. Such a distribution makes it unlikely that stapedial morphology can be used to separate edentates from other eutherian mammals.


2019 ◽  
Vol 99 (4) ◽  
pp. 701-722 ◽  
Author(s):  
Lars W. van den Hoek Ostende ◽  
Peter Joniak ◽  
Bora Rojay ◽  
Cathelijn Aten ◽  
Melike Bilgin ◽  
...  

1989 ◽  
Vol 67 (6) ◽  
pp. 1903-1915 ◽  
Author(s):  
E. E. McIver ◽  
J. F. Basinger

Fossil foliage and seed cones of Thuja (Cupressaceae) have been discovered in early Tertiary (Paleocene) sediments of the Eureka Sound Group on Ellesmere Island, Canadian Arctic Archipelago. Vegetative remains of the fossil species, Thuja polaris sp.nov., bear alternately branched, moderately divided, flattened, and pinnatelike sprays with scale-like, decussate leaves. Seed cones are oblong, bearing 8 – 9 pairs of thin, probably leathery cone scales with distinct, reflexed umbos. Fossil cones and foliage resemble closely those of extant Thuja plicata. However, fossil seed cones have twice as many pairs of scales as do extant species of Thuja. A review of the fossil record indicates that most Thuja-like vegetative remains which have been reported from Cretaceous and Tertiary deposits in the Northern Hemisphere are best assigned to form taxa and not to extant genera. Reproductive material from four Tertiary localities can be assigned to Thuja on the basis of seed cone structure. The evolutionary history of the genus, based on fossil and extant seed cone morphology, appears to include a reduction in the number of cone scales. Extant species form a closely related, natural group and, with the exception of T. sutchuenensis, may have arisen from an ancestor similar to T. polaris. Although Thuja was widespread in the Northern Hemisphere during much of the Tertiary, the genus is now confined to northeastern and northwestern North America, and to Japan, Korea, and central China.


Author(s):  
Vitali Bartash

Region:    Southern Mesopotamia = Sumer.Period:     Ca. 3200-2000 BC, i.e. Early Bronze Age.Sources:    Administrative cuneiform texts from temple and palace archives.Subject:    Children of low-rank social status in temple and palace households. Aims:   1) Systematize the terminology for children and offer an overview of its development.2) Identify what biological social characteristics of children are hiding behind these terms.3) Recognize the characteristic features in the terminology for children. Methods: Philological, historical, sociological (sex-age groups/classes). Key facts:   1) Children as dependents in central households appear in cuneiform records as early as the Uruk IV Period (ca. 3350-3250 BC).2) The documents enable to reconstruct several sets of terms to describe human resources in temple and palace households. A substantial part of these terms describe two main biological characteristics of children: their sex and age group.3) Originally, during the earliest periods, the terminology for humans and children in particular bore a strong resemblance with the terms for animals, which implies that the former is an offshoot of the latter.Main point: Other age groups, adults and elderly, received specific terms that were reserved exclusively to designate these age groups. The striking fact conclusion about the child terminology is that it obstinately remained dependent on the terminology for animal youth.The comparison of the bureaucratic terms for children with the lexical evidence (“ancient dictionaries”) demonstrates that the rich selection of terms within the field “children/childhood” that existed in the Sumerian society did not find reception in the administrative practice. 


1997 ◽  
Vol 40 (3) ◽  
Author(s):  
A. Barka ◽  
R. Reilinger

This paper reviews the main tectonic features of the Eastern Mediterranean region combining the recent information obtained from GPS measurements, seismicity and neotectonic studies. GPS measurements reveal that the Arabian plate moves northward with respect to Eurasia at a rate of 23 ± 1 mm/yr, 10 mm/yr of this rate is taken up by shortening in the Caucasus. The internal deformation in Eastern Anatolia by conjugate strike-slip faulting and E-W trending thrusts, including the Bitlis frontal thrust, accommodates approximately a 15 mm/yr slip rate. The Northeast Anatolian fault, which extends from the Erzincan basin to Caucasus accommodates about 8 ± 5 mm/yr of left-lateral motion. The neotectonic fault pattern in Eastern Anatolia suggests that the NE Anatolian block moves in an E-ENE direction towards the South Caspian Sea. According to the same data, the Anatolian-Aegean block is undergoing a counter-clockwise rotation. However, from the residuals it appears that this solution can only be taken as a preliminary approximation. The Eulerian rotation pole indicates that slip rate along the North Anatolian fault is about 26 ± 3 mm/yr. This value is 10 mm/yr higher than slip rates obtained from geological data and historical earthquake records and it includes westward drift of the Pontides of a few millimetres/year or more. GPS measurements reveal that the East Anatolian fault accommodates an 11 ± 1 mm/yr relative motion. GPS data suggest that Central Anatolia behaves as a rigid block, but from neotectonic studies, it clearly appears that it is sliced by a number of conjugate strike-slip faults. The Isparta Angle area might be considered a major obstacle for the westward motion of the Anatolian block (Central and Eastern Anatolia). The western flank of this geological structure, the Fethiye-Burdur fault zone appears to be a major boundary with a slip rate of 15-20 mm/yr. The Western Anatolian grabens take up a total of 15 mm/yr NE-SW extension. The fact that motions in Central Anatolia relative to Eurasia, are 15-20 mm/yr while in Western Anatolia and Aegean Sea they are 30-40 mm/yr could suggest that Western Anatolia decouples from Central Anatolia and the Isparta Angle by the Fethiye-Burdur fault zone and Eski?ehir fault. It is also hypothesized that the differentiation of tectonic styles and velocities in the Anatolian-Aegean block are related to differences between the slabs lying under the Cyprus and Hellenic arcs.


Fossil Record ◽  
2021 ◽  
Vol 24 (2) ◽  
pp. 339-346
Author(s):  
Valentine Bouju ◽  
Simon Rosse-Guillevic ◽  
Marion Griffon ◽  
Błażej Bojarski ◽  
Jacek Szwedo ◽  
...  

Abstract. A new, extinct species of Allodia Winnertz is described from early Miocene amber of Ethiopia. Allodia paleoafricana sp. nov. is mostly characterized by the scutum with strong anteromarginal, dorsocentral, and lateral setae and the wing with the stem of the M-fork slightly shorter than the vein r–m and the base of the M4–CuA fork aligned with the base of r–m. The assignment to any of the two subgenera Allodia stricto sensu or Brachycampta Winnertz remains equivocal as the fossil intermingles traits found in both taxa. Allodia is known mostly from the Palearctic region, while only a few species have been described from Africa. In this regard, the new fossil species from Ethiopia brings significant new information regarding the Afrotropical distribution and natural history of the genus.


2020 ◽  
Vol 3 (5) ◽  
pp. 1233-1248
Author(s):  
A. V. Safronov

The article deals with the Sea Peoples’ migrations at the beginning of 12th century BC. It is based on ancient Egyptian written sources, archaeological data and Greek narrative tradition. The author tries to reconstruct the general stages of Late Bronze Age ethnical movements in the Aegean and Eastern Mediterranean at the end of the 13th – beginning the 12th centuries BC. The author shows that the Sea peoples’ movement was not homogeneous. Moreover, not all the Sea Peoples can be considered as migrants. The tribes of Shekelesh and Weshesh were the typical sea raiders who plundered the rich centres of the Eastern Mediterranean. The possible reason for the Peleset, Theker and Turša migration seems to be the war which devastated their homeland in north-eastern Anatolia between 1208/1203 и 1195 BC. The appearance of the Denyen in Sea Peoples’ movement must be connected with the destructions of Mycenaean centres in Southern Greece circa 1200 BC. Their inhabitants left their homeland and migrated to the different regions of the Aegean, Anatolia, Eastern and Western Mediterranean. The Sea Peoples’ migrations were only the first stage of global ethnic movements in Eurasia at the end of the Bronze Age which totally changed the ethnopolitical map of Southern Europe, Anatolia and Eastern Mediterranean.


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