A Middle Permian–Middle Triassic accretionary complex and a Late Triassic foredeep basin: Forerunners of an Indosinian (Late Triassic) thrust complex in the Thailand–Malaysia border area

2013 ◽  
Vol 76 ◽  
pp. 99-114 ◽  
Author(s):  
Michael F. Ridd
2017 ◽  
Vol 8 (3) ◽  
pp. 599-600
Author(s):  
Wenjiao Xiao ◽  
Miao Sang ◽  
Apas Bakirov ◽  
Rustam Orozbaev

2012 ◽  
Vol 2012 ◽  
pp. 1-14 ◽  
Author(s):  
María Belén Lara ◽  
Oscar Florencio Gallego ◽  
Lara Vaz Tassi

The order Coleoptera is the most diversified group of the Class Insecta and is the largest group of the Animal Kingdom. This contribution reviews the Mesozoic insects and especially the coleopteran records from Argentina, based on bibliographical and unpublished materials (86 described species, 526 collected specimens). The material came from different geological units from the late Middle Triassic to the Late Triassic (Bermejo, Cuyo, and Malargüe basins) to the Middle-Late Jurassic and Early Cretaceous (Deseado Massif, Cañadón Asfalto, and San Luís Basin). The coleopteran record is composed of 29 described species with 262 collected specimens (isolated elytra) mainly represented by Triassic species and only four specimens recorded in Jurassic units, all of them currently unpublished. These fossil coleopterans provide fundamental information about the evolution of insects in the Southern Hemisphere and confirm the Triassic Argentinean insect deposits to be among the most important in the world.


2021 ◽  
Author(s):  
Victoria S. Engelschiøn ◽  
Øyvind Hammer ◽  
Fredrik Wesenlund ◽  
Jørn H. Hurum ◽  
Atle Mørk

<p>Several carbon isotope curves were recently published for the Early and Middle Triassic in Tethys. Recent work has also been done on the Early Triassic of Svalbard, but not yet for the Middle Triassic. This work is the first to measure δ<sup>13</sup>C for different Middle Triassic localities on Svalbard, which was then part of the Boreal Ocean on northern Pangea. Our aim is to understand the controls on the Svalbard carbon isotope curve and to place them in a global setting.</p><p>Correlating Triassic rocks around the world is interesting for several reasons. The Triassic Period was a tumultuous time for life, and the Arctic archipelago of Svalbard has shown to be an important locality to understand the early radiation of marine vertebrates in the Triassic. Much effort is also made to understand the development of the Barents Sea through Svalbard’s geology.</p><p>Carbon isotope curves are controlled by depositional environment and global fluctuations. Global factors such as the carbon cycle control the long-term carbon isotopic compositions, while short-term fluctuations may reflect the origin of organic materials in the sediment (e.g. algal or terrestrial matter), stratification of the water column, and/or surface water productivity. Carbon isotopes can therefore be useful to understand the depositional environment and to correlate time-equivalent rocks globally.</p><p>The dataset was collected through three seasons of fieldwork in Svalbard with localities from the islands Spitsbergen, Edgeøya and Bjørnøya. Detailed stratigraphic sampling has resulted in high-resolution δ<sup>13</sup>C curves. These show three strong transitions; 1) on the boundary between the Early and Middle Triassic, 2) in the middle of the formation and 3) at the Middle and Late Triassic boundary. Several Tethyan localities show a possibly similar Early-Middle Triassic signal. Current work in progress is sedimentological analysis by thin sections and X-ray fluorescence spectroscopy (XRF) to further understand the sedimentary environment.</p>


1992 ◽  
Vol 6 ◽  
pp. 155-155
Author(s):  
Kotaro Kamada

Before opening of the Japan Sea, the Japanese islands were attached to the eastern margin of the Asian continent. The Southern Kitakami Belt is regarded as a micro-continent in an accretional complex of the islands, that accreted before the Early Cretaceous. But its tectonic setting and location between the belt and the Asian continent is still an unresolved argument.Permo-Triassic sequences in the Southern Kitakami Belt are composed of shallow to off-shore deposits. These deposits are composed of clastics, carbonates with volcaniclastics. But there was no volcanic activity in the belt in the Middle to Late Permian. From the viewpoint of the sedimentary character and history, the Middle Permian to Middle Triassic sequences differ from their previous and their following successions in the belt. And the sedimentary basin of Middle Permian to Middle Triassic was bounded by transform faults. Magmatic arc was replaced by passive margin as hinterland of the Southern Kitakami Belt during the Middle Permian to Middle Triassic. It means that the sedimentary basin moved from the margin of Yangtze Platform to Sino-Korean Platform at that time.


The rhynchosaur Rhynchosaurus articeps Owen, 1842, from the Middle Triassic of Grinshill, northern Shropshire, England, was a small reptile, about 0.5 m long. About 17 individual animals are represented by skulls, complete skeletons and partial skeletons, and these have permitted detailed restorations. The skull (60-80 mm long) is low and broad at the back, and it shows all of the typical rhynchosaur features of beak-like premaxillae, single median naris, fused parietal, broad maxillary tooth plate and dentary, both with multiple rows of teeth, and a deep lower jaw. The skeleton shows adaptations for fast terrestrial locomotion with a semi-erect hindlimb posture and for scratch-digging with the hind-foot. The skeleton is relatively more slender than that of most other middle and late Triassic rhynchosaurs, but this is probably an allometric effect of its much smaller size (they are typically 1-2 m long). A further species of Rhynchosaurus from Warwick, named here R. brodiei , is represented by 15 specimens of partial skulls, tooth-bearing elements, and isolated postcranial bones. It was slightly larger than R. articeps , with a typical skull length of 90 mm, and estimated body length of 0.6 m, but the skull length ranged up to 140 mm. It differs from R. articeps in having a much larger jugal in the cheek area, and in the greater height and breadth of the skull. The isolated maxillary fragments from Bromsgrove probably also belong to R. brodiei . The third species of Rhynchosaurus from Devon, named here R. spenceri , is now known from numerous specimens of at least 25 individuals, most of which were collected recently. These show a range in estimated skull length from 40 to 170 mm, but most specimens are at the upper end of that range, with an average skull length of 140 mm, and an estimated total body length of 0.9-1.0 m R. spenceri differs from R. articeps and R. brodiei in having a skull that is broader than it is long (otherwise a character of late Triassic rhynchosaurs), and it shares the large jugal character with R. brodiei . Teeth are not well preserved in R. articeps, but several specimens of R. brodiei and R. spenceri give detailed information. The pattern of wear, and the nature of the jaw joint, suggest that Rhynchosaurus had a precision-shear bite, as in other rhynchosaurs, with no back and forwards motion. The maxilla had two grooves, a major and a minor one, which received two matching ridges of the dentary on occlusion. The multiple rows of teeth on maxilla and dentary, and the surrounding bone, wore down as uniform units. The diet was probably tough vegetation, which was dug up by scratch-digging, raked together with the hands or the premaxillary beak, and manipulated in the mouth by a strong tongue. Rhynchosaurus is found variously in fluvial-intertidal deposits with evidence of desiccation (Grinshill, Warwick, Bromsgrove), and fluvial-aeolian deposits laid down in arid conditions with occasional flash floods (Devon). The bones have generally been transported (Warwick, Bromsgrove, Devon), but the Grinshill specimens are largely complete and undisturbed. The associated floras and faunas at Warwick, Bromsgrove, and Devon include pteridophytes, gymnospermopsids, bivalves, scorpions, freshwater fish, temnospondyl amphibians and reptiles (macrocnemids, thecodontians, ?procolophonids). Rhynchosaurs are archosauromorph diapsids, possibly related to the enigmatic Trilophosaurus, and a sister group to Prolacertiformes + Archosauria. A cladistic analysis of Rhynchosauria reveals one major subgroup, the Hyperodapedontinae ( Hyperodapedonand and Scaphonyx ), which is late Triassic in age. The earlier rhynchosaurs, including the middle Triassic Stenaulorhynchus and Rhynchosaurus , appear to form successively closer outgroups to the Hyperodapedontinae. The three species of Rhynchosaurus share only one possible synapomorphy in comparison with Stenaluorhynchus : The dentary is well over half the length of the lower jaw. The ‘Rhynchosaurinae’ ( Stenaulorhynchus and Rhynchosaurus ) was not established as a monophyletic group in the present analysis. These two genera share two postulated synapomorphies: the occipital condyle lies well in front of the quadrates, and there are two grooves on the maxilla and two ridges on the dentary. A third postulated synapomorphy, the presence of a single row of teeth on the pterygoid, has not been confirmed in this study for either Rhynchosaurus or Stenaulorhynchus . However, these postulated synapomorphies are outweighed by the synapomorphies that Rhynchosaurus shares with the Hyperodapedontinae. The specimens of Rhynchosaurus have been used as biostratigraphic indicators for the English middle Triassic, indicating Anisian to early Ladinian ages. The three species can be arranged in a sequence from ‘most prim itive’ to ‘most advanced’, but this cannot be used confidently to give a stratigraphic sequence.


1992 ◽  
Vol 6 ◽  
pp. 202-202 ◽  
Author(s):  
Ricardo N. Martínez ◽  
Catherine A. Forster ◽  
Cathleen L. May

Two skulls representing new forms of carnivorous cynodonts were discovered recently in the Upper Triassic (Carnian) Ischigualasto Formation of northwestern Argentina. These specimens are the first complete carnivorous cynodonts described from the Late Triassic of Argentina, and provide critical evidence for the evolution of cranial form between well known Middle Triassic cynodonts, such as Probainognathus, and the first mammals in the latest Triassic.The first skull (PVSJ 422) is proportionately long, with a posterior skull width only 35 per cent of basal skull length (9.5 cm.). Other distinctive features of the skull include the form of the postcanine crowns, which have two cusps posterior to the principal cusp and fine serations on their leading edges, and which overlap each other in an imbricate pattern. Postcanines 5-7 are subequal in size, overlap the dentary laterally, and are substantially larger than postcanines 2-4. The dental formula in the upper jaw is I4-C1-PC7, with the small first postcanine separated fore and aft by small diastemas. As in other advanced eucynodonts, no pineal foramen is present. Some postcranial elements, as yet unstudied, were also found with this specimen.The second skull (PVSJ 411) has broader proportions, the width between quadrates almost half that of basal skull length (7.5 cm.). These proportions, in combination with deep, curved zygomatic arches, resemble other Middle Triassic cynodonts such as Probelesodon. Distinctive features of this skull include bicusped postcanines in the upper jaw similar to those of Probelesodon, and a mandibular symphysis that extends back to the level of the fourth postcanine. The dental formula in the upper jaw is I4-C1-PC6. As in the first skull, a pineal foramen is absent.Several advanced cranial features, such as a fused mandibular symphysis, occur in both skulls and strongly suggest that these new forms belong within the Eucynodontia (Hopson, 1991). Other advanced features, such as the absence of a pineal foramen, further suggest that these new forms are closer to mammals than are traversodontid cynodonts. In contrast, other characters appear to be curiosly primitive, such as a short hard palate in the first skull. These new cynodonts thus may introduce previously unseen features and character combinations to the study of cynodont cranial evolution.


Paleobiology ◽  
1992 ◽  
Vol 18 (1) ◽  
pp. 50-79 ◽  
Author(s):  
Benjamin J. Greenstein

The class Echinoidea apparently originated during the Ordovician Period and diversified slowly through the Paleozoic Era. The clade then mushroomed in diversity beginning in Late Triassic time and continued expanding into the present. Although this evolutionary history is generally accepted, the taphonomic overprint affecting it has not been explored. To gain a more accurate perception of the evolutionary history of the group, I have compared the diversity history of the family Cidaridae (Echinodermata: Echinoidea) with the preservational style of fossil type species using literature-derived data. The Cidaridae apparently originated in Middle Triassic time and diversified slowly through the Neocomian (Early Cretaceous). Diversity was maintained through the remainder of the Cretaceous and Tertiary Periods, reflecting the diversity history of the subclass. Characterization of the preservational style of type fossil material for the family revealed the following breakdown of preservational states: 60% of species were described on the basis of disarticulated skeletal material, primarily spines; 20% based on intact coronas denuded of spines, apical system, Aristotle's lantern and peristomial plates; 10% based on large coronal fragments; and 10% based on other skeletal elements. This distribution may represent the effect of a disarticulation threshold on the condition of echinoid carcasses before final burial and suggests that preservation of intact specimens may be very unlikely. For cidaroids, previous work has suggested that this threshold is likely to be reached after 7 days of decay.Comparison of the diversity history of the Cidaridae with the preservation data reveals that characteristic patterns of taphonomic overprint have affected the group since its origination in Middle Triassic time, and the nature of that overprint has changed over time: the early diversity history of the group is characterized by occurrences of fragmented fossil material, with spines predominant; further radiation of the group in mid-Jurassic time coincided with an increase in modes of preservation, ranging between exceptionally well-preserved material and disarticulated skeletal elements. Finally, type material is more rarely described from younger stratigraphic intervals (Miocene–Pleistocene) and consists predominantly of disarticulated skeletal elements and coronal fragments larger than an interambulacrum in size. Intact, denuded coronas are noticeably lacking.The number of type species of Cidaridae described in each stratigraphic interval has not been consistent during post-Paleozoic time. Middle Triassic, Malm (Upper Jurassic), Senonian (Upper Cretaceous) and Eocene series yielded significantly (α = .05) higher numbers of type specimens per million years, while the Lias (Lower Jurassic), Dogger (Mid-Jurassic), Lower Cretaceous and Paleocene yielded significantly (α = .05) lower numbers of type specimens per million years. This may be the result of a combination of taxonomic, sampling, and geographical biases.


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