Stratigraphy and Palaeogeography of Lower Triassic in Poland on the Bassis of Megaspores
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Geothermal Fluid and Reservoir Properties in the Upper Rhine Graben
Geothermal fluid and reservoir properties in the Upper Rhine Graben Ingrid Stober Institut für Angewandte Geowissenschaften – Abteilung Geothermie Strasbourg, 5. Februar 2015 1 KIT – Universität des Landes Baden-Württemberg und Institut für Angewandte Geowissenschaften - nationales Forschungszentrum in der Helmholtz-Gemeinschaft Abteilungwww.kit.edu Geothermie Geological situation of the Upper Rhine Graben During Early Cenozoic and Late Eocene: • Subsidence of Upper Rhine Graben • Uplift of Black Forest and Vosges mountains as Rift flanks Uplift (several km) caused erosion on both flanks of the Graben, exhuming gneisses and granites. The former sedimentary cover is conserved within the Graben. The deeply burried sediments include several aquifers containing hot water. Additionally there are thick Tertiary and Quaternary sediments, formed during the subsidence of the Graben. 2 Prof. Dr. Ingrid Stober Institut für Angewandte Geowissenschaften - Abteilung Geothermie Complex hydrogeological situation in the Graben • Broken layers, partly with hydraulic connection, partly without • Alternation between depression areas & elevated regions (horst – graben – structure) • Hydraulic behavior of faults unknown • There are extensional as well as compressive faults • Main faults show vertical displacements of several 1,000 meters • Thickness of the individual layers not constant. 3 Prof. Dr. Ingrid Stober Institut für Angewandte Geowissenschaften - Abteilung Geothermie Hydrogeology • Thickness of the individual layers not constant • Hauptrogenstein -
Biochronology of the Triassic Tetrapod Footprints
Geological Society, London, Special Publications Tetrapod footprints - their use in biostratigraphy and biochronology of the Triassic Hendrik Klein and Spencer G. Lucas Geological Society, London, Special Publications 2010; v. 334; p. 419-446 doi:10.1144/SP334.14 Email alerting click here to receive free email alerts when new articles cite this service article Permission click here to seek permission to re-use all or part of this article request Subscribe click here to subscribe to Geological Society, London, Special Publications or the Lyell Collection Notes Downloaded by on 15 June 2010 © 2010 Geological Society of London Tetrapod footprints – their use in biostratigraphy and biochronology of the Triassic HENDRIK KLEIN1,* & SPENCER G. LUCAS2 1Ru¨bezahlstraße 1, D-92318 Neumarkt, Germany 2New Mexico Museum of Natural History, 1801 Mountain Road NW, Albuquerque, NM 87104-1375 USA *Corresponding author (e-mail: [email protected]) Abstract: Triassic tetrapod footprints have a Pangaea-wide distribution; they are known from North America, South America, Europe, North Africa, China, Australia, Antarctica and South Africa. They often occur in sequences that lack well-preserved body fossils. Therefore, the question arises, how well can tetrapod footprints be used in age determination and correlation of stratigraphic units? The single largest problem with Triassic footprint biostratigraphy and biochronology is the non- uniform ichnotaxonomy and evaluation of footprints that show extreme variation in shape due to extramorphological (substrate-related) phenomena. Here, we exclude most of the countless ichnos- pecies of Triassic footprints, and instead we consider ichnogenera and form groups that show distinctive, anatomically-controlled features. Several characteristic footprint assemblages and ichnotaxa have a restricted stratigraphic range and obviously occur in distinct time intervals. -
32-38 Oldham Road, Ancoats, Manchester, Greater Manchester
32-38 Oldham Road, Ancoats, Manchester, Greater Manchester Archaeological Building Investigation Final Report Oxford Archaeology North November 2007 CgMs Consulting Issue No: 2007-08/741 OA North Job No: L9887 NGR: SJ 8475 9876 32-38 Oldham Road, Ancoats, Manchester: Archaeological Building Investigation Final Report 1 CONTENTS SUMMARY .....................................................................................................................2 ACKNOWLEDGEMENTS.................................................................................................3 1. INTRODUCTION.........................................................................................................4 1.1 Circumstances of the Project.............................................................................4 1.2 Site Location and Geology................................................................................4 2. METHODOLOGY........................................................................................................5 2.1 Methodology .....................................................................................................5 2.2 Archive..............................................................................................................5 3. HISTORICAL BACKGROUND .....................................................................................6 3.1 Background .......................................................................................................6 3.2 Development of Ancoats...................................................................................7 -
GUIDEBOOK the Mid-Triassic Muschelkalk in Southern Poland: Shallow-Marine Carbonate Sedimentation in a Tectonically Active Basin
31st IAS Meeting of Sedimentology Kraków 2015 GUIDEBOOK The Mid-Triassic Muschelkalk in southern Poland: shallow-marine carbonate sedimentation in a tectonically active basin Guide to field trip B5 • 26–27 June 2015 Joachim Szulc, Michał Matysik, Hans Hagdorn 31st IAS Meeting of Sedimentology INTERNATIONAL ASSOCIATION Kraków, Poland • June 2015 OF SEDIMENTOLOGISTS 225 Guide to field trip B5 (26–27 June 2015) The Mid-Triassic Muschelkalk in southern Poland: shallow-marine carbonate sedimentation in a tectonically active basin Joachim Szulc1, Michał Matysik2, Hans Hagdorn3 1Institute of Geological Sciences, Jagiellonian University, Kraków, Poland ([email protected]) 2Natural History Museum of Denmark, University of Copenhagen, Denmark ([email protected]) 3Muschelkalk Musem, Ingelfingen, Germany (encrinus@hagdorn-ingelfingen) Route (Fig. 1): From Kraków we take motorway (Żyglin quarry, stop B5.3). From Żyglin we drive by A4 west to Chrzanów; we leave it for road 781 to Płaza road 908 to Tarnowskie Góry then to NW by road 11 to (Kans-Pol quarry, stop B5.1). From Płaza we return to Tworog. From Tworog west by road 907 to Toszek and A4, continue west to Mysłowice and leave for road A1 then west by road 94 to Strzelce Opolskie. From Strzelce to Siewierz (GZD quarry, stop B5.2). From Siewierz Opolskie we take road 409 to Kalinów and then turn we drive A1 south to Podskale cross where we leave south onto a local road to Góra Sw. Anny (accomoda- for S1 westbound to Pyrzowice and then by road 78 to tion). From Góra św. Anny we drive north by a local road Niezdara. -
Gondwana Vertebrate Faunas of India: Their Diversity and Intercontinental Relationships
438 Article 438 by Saswati Bandyopadhyay1* and Sanghamitra Ray2 Gondwana Vertebrate Faunas of India: Their Diversity and Intercontinental Relationships 1Geological Studies Unit, Indian Statistical Institute, 203 B. T. Road, Kolkata 700108, India; email: [email protected] 2Department of Geology and Geophysics, Indian Institute of Technology, Kharagpur 721302, India; email: [email protected] *Corresponding author (Received : 23/12/2018; Revised accepted : 11/09/2019) https://doi.org/10.18814/epiiugs/2020/020028 The twelve Gondwanan stratigraphic horizons of many extant lineages, producing highly diverse terrestrial vertebrates India have yielded varied vertebrate fossils. The oldest in the vacant niches created throughout the world due to the end- Permian extinction event. Diapsids diversified rapidly by the Middle fossil record is the Endothiodon-dominated multitaxic Triassic in to many communities of continental tetrapods, whereas Kundaram fauna, which correlates the Kundaram the non-mammalian synapsids became a minor components for the Formation with several other coeval Late Permian remainder of the Mesozoic Era. The Gondwana basins of peninsular horizons of South Africa, Zambia, Tanzania, India (Fig. 1A) aptly exemplify the diverse vertebrate faunas found Mozambique, Malawi, Madagascar and Brazil. The from the Late Palaeozoic and Mesozoic. During the last few decades much emphasis was given on explorations and excavations of Permian-Triassic transition in India is marked by vertebrate fossils in these basins which have yielded many new fossil distinct taxonomic shift and faunal characteristics and vertebrates, significant both in numbers and diversity of genera, and represented by small-sized holdover fauna of the providing information on their taphonomy, taxonomy, phylogeny, Early Triassic Panchet and Kamthi fauna. -
Fossil Middle Triassic “Sea Cows” – Placodont Reptiles As Macroalgae Feeders Along the North-Western Tethys Coastline with Pangaea and in the Germanic Basin
Vol.3, No.1, 9-27 (2011) Natural Science http://dx.doi.org/10.4236/ns.2011.31002 Fossil middle triassic “sea cows” – placodont reptiles as macroalgae feeders along the north-western Tethys coastline with Pangaea and in the Germanic basin Cajus G. Diedrich Paleologic, Nansenstr, Germany; [email protected] Received 19 October 2010; revised 22 November 2010; accepted 27 November 2010. ABSTRACT this plant-feeding adaptation and may even ex- plain the origin or at least close relationship of The descriptions of fossil Triassic marine pla- the earliest Upper Triassic turtles as toothless codonts as durophagous reptiles are revised algae and jellyfish feeders, in terms of the through comparisons with the sirenia and basal long-term convergent development with the si- proboscidean mammal and palaeoenvironment rens. analyses. The jaws of placodonts are conver- gent with those of Halitherium/Dugong or Mo- Keywords: Placodont Reptiles; Triassic; eritherium in their general function. Whereas Convergent Evolutionary Ecological Adaptation; Halitherium possessed a horny oral pad and Sirenia; Macroalgae Feeders; NW Tethys Shelf; counterpart and a special rasp-like tongue to Palaeoecology grind seagrass, as does the modern Dugong, placodonts had large teeth that covered their 1. INTRODUCTION jaws to form a similar grinding pad. The sirenia also lost their anterior teeth during many Mil- The extinct reptile group of the placodonts found in lions of years and built a horny pad instead and Germany and other European sites (Figure 1), a group specialized tongue to fed mainly on seagrass, of diverse marine diving reptiles, had large teeth cover- whereas placodonts had only macroalgae availa- ing the lower and complete upper jaws (Figsure 2-5) ble. -
Paper Number: 1591 the Stratigraphic Table of Germany Revisited: 2016
Paper Number: 1591 The Stratigraphic Table of Germany revisited: 2016 Menning, M., Hendrich, A. & Deutsche Stratigraphische Kommission Helmholtz-Zentrum Potsdam, Deutsches GeoForschungsZentrum GFZ, D-14473 Potsdam, Germany, menne@gfz- potsdam.de For the occasion of the “Year of Geosciences” in Germany 2002 the German Stratigraphic Commission created the “Stratigraphic Table of Germany 2002” (STD 2002) [1]. It presents more than 1 000 geological units, beds, formations, groups, regional stages, and regional series of the Regional Stratigraphic Scale (RSS) of Central Europe in relation to the Global Stratigraphic Scale (GSS). Alongside the recent stratigraphic terms are also some historical names like Wealden (now Bückeberg Formation, Early Cretaceous) and Wellenkalk (now Jena Formation, Muschelkalk Group, Middle Triassic) [1] (http://www.stratigraphie.de/std2002/download/STD2002_large.pdf). The numerical ages in the table have been estimated using all available time indicators including (1) radio-isotopic ages, (2) sedimentary cycles of the Milankovich-band of about 0.1 Ma and 0.4 Ma duration for the Middle Permian to Middle Triassic (Rotliegend, Zechstein, Buntsandstein, Muschelkalk, and Keuper groups), and (3) average weighted thicknesses for the Late Carboniferous of the Central European Namurian, Westphalian, and Stephanian regional stages. Significant uncertainties are indicated by arrows instead of error bars as in the Global Time Scales 1989 and 2012 (GTS 1989, Harland et al. 1990 [2], GTS 2012, Gradstein et al. 2012 [3]). Those errors were underestimated in the GTS 2012 [3] because they were calculated using too much emphasis on laboratory precision of dating and less on the uncertainty of geological factors. Figure 1: Buntsandstein and Muschelkalk in the Stratigraphic Table of Germany 2016 (part) In 2015 und 2016 the German Stratigraphic Commission updated the entire STD 2002 [1]. -
Burrows of Enteropneusta in Muschelkalk (Middle Triassic) of the Holycross Mountains, Poland
ACT A PAL A EON T 0 LOG I CAP 0 LON ICA Vol. XIV 1969 No.2 JOZEF KAZMIERCZAK & ANDRZEJ PSZCZOLKOWSKI BURROWS OF ENTEROPNEUSTA IN MUSCHELKALK (MIDDLE TRIASSIC) OF THE HOLYCROSS MOUNTAINS, POLAND Abstract. - Traces of burrowing organisms from Lower Muschelkalk carbonate sediments of the Holy Cross Mountains (Gory SWi~tokrzyskie) interpreted as burrow systems of enteropneusts, have been described. Morphological and palaeoecological analysis of Triassic forms based on the comparison with the burrows of Recent enteropneusts is given. The presence of many horizons with burrows of entero pneusts in the profiles of the Lower Muschelkalk deposits (Lukowa beds) and the lithological characters of these deposits seem to indicate that the sedimentation took place in a zone of the basin affected by the activity of tidal current~. INTRODUCTION During field studies on biofacies of the Mesozoic border of the Holy Cross Mountains (Gory Swi~tokrzyskie) many traces of burrowing orga nisms were found by the present writers in the Lower Muschelkalk sedi ments. After a close examination, it turned out that these structures might be almost unequivocally identified with burrow systems of Recent entero pneusts. The field observations covered the environs of Wincentow and Polichno in the western part of the Holy Cross region and outcrops of the Lower Muschelkalk in the southwestern limb of Zbrza anticline (Text-fig. 1). According to a lithostratigraphical division of the Lower Muschel kalk in the Holy Cross Mountains (Senkowiczowa, 1957, 1959, 1961), the burrows observed occur primarily in Lukowa beds (Text-fig. 1). The most important aim of this work was to describe and interpret the burrows of enteropneusts, but the present writers have also given their observations concerning lithological characters of Lukowa beds. -
Lower Triassic Reservoir Development in the Northern Dutch Offshore
Downloaded from http://sp.lyellcollection.org/ by guest on September 29, 2021 Lower Triassic reservoir development in the northern Dutch offshore M. KORTEKAAS1*, U. BÖKER2, C. VAN DER KOOIJ3 & B. JAARSMA1 1EBN BV Daalsesingel 1, 3511 SV Utrecht, The Netherlands 2PanTerra Geoconsultants BV, Weversbaan 1-3, 2352 BZ Leiderdorp, The Netherlands 3Utrecht University, Budapestlaan 4, 3584 CD Utrecht, The Netherlands *Correspondence: [email protected] Abstract: Sandstones of the Main Buntsandstein Subgroup represent a key element of the well- established Lower Triassic hydrocarbon play in the southern North Sea area. Mixed aeolian and fluvial sediments of the Lower Volpriehausen and Detfurth Sandstone members form the main res- ervoir rock, sealed by the Solling Claystone and/or Röt Salt. It is generally perceived that reservoir presence and quality decrease towards the north and that the prospectivity of the Main Buntsandstein play in the northern Dutch offshore is therefore limited. Lack of access to hydrocarbon charge from the underlying Carboniferous sediments as a result of the thick Zechstein salt is often identified as an additional risk for this play. Consequently, only a few wells have tested Triassic reservoir and therefore this part of the basin remains under-explored. Seismic interpretation of the Lower Volprie- hausen Sandstone Member was conducted and several untested Triassic structures are identified. A comprehensive, regional well analysis suggests the presence of reservoir sands north of the main fairway. The lithologic character and stratigraphic extent of these northern Triassic deposits may suggest an alternative reservoir provenance in the marginal Step Graben system. Fluvial sands with (local) northern provenance may have been preserved in the NW area of the Step Graben system, as seismic interpretation indicates the development of a local depocentre during the Early Triassic. -
A New Large Capitosaurid Temnospondyl Amphibian from the Early Triassic of Poland
A new large capitosaurid temnospondyl amphibian from the Early Triassic of Poland TOMASZ SULEJ and GRZEGORZ NIEDŹWIEDZKI Sulej, T. and Niedźwiedzki, G. 2013. A new large capitosaurid temnospondyl amphibian from the Early Triassic of Po− land. Acta Palaeontologica Polonica 58 (1): 65–75. The Early Triassic record of the large capitosaurid amphibian genus Parotosuchus is supplemented by new material from fluvial deposits of Wióry, southern Poland, corresponding in age to the Detfurth Formation (Spathian, Late Olenekian) of the Germanic Basin. The skull of the new capitosaurid shows an “intermediate” morphology between that of Paroto− suchus helgolandicus from the Volpriehausen−Detfurth Formation (Smithian, Early Olenekian) of Germany and the slightly younger Parotosuchus orenburgensis from European Russia. These three species may represent an evolutionary lineage that underwent a progressive shifting of the jaw articulation anteriorly. The morphology of the Polish form is dis− tinct enough from other species of Parotosuchus to warrant erection of a new species. The very large mandible of Parot− osuchus ptaszynskii sp. nov. indicates that this was one of the largest tetrapod of the Early Triassic. Its prominent anatomi− cal features include a triangular retroarticular process and an elongated base of the hamate process. Key words: Temnospondyli, Capitosauridae, Buntsandstein, Spathian, Olenekian, Triassic, Holy Cross Mountains, Poland. Tomasz Sulej [[email protected]], Institute of Paleobiology, Polish Academy of Sciences, ul. Twarda 51/55, PL−00−818 Warszawa, Poland; Grzegorz Niedźwiedzki [[email protected]], Institute of Paleobiology, Polish Academy of Sciences, ul. Twarda 51/55, PL−00−818 Warszawa, Poland; current addresses: Department of Organismal Biology, Uppsala Uni− versity, Norbyvägen 18A, 752 36 Uppsala, Sweden and Department of Paleobiology and Evolution, Faculty of Biology, University of Warsaw, ul. -
Facies Types and Depositional Environments of a Morphologically
Annales Societatis Geologorum Poloniae (2016), vol. 86: 119-164. doi: http://dx.doi.org/10.14241/asgp.2016.013 FACIES TYPES AND DEPOSITIONAL ENVIRONMENTS OF A MORPHOLOGICALLY DIVERSE CARBONATE PLATFORM: A CASE STUDY FROM THE MUSCHELKALK (MIDDLE TRIASSIC) OF UPPER SILESIA, SOUTHERN POLAND Michał MATYSIK Institute o f Geological Sciences, Jagiellonian University, Oleandry 2a, 30-063 Kraków, Poland Present address: Natural History Museum, University of Copenhagen, 0ster Voldgade 5-7, DK-1350 Copenhagen K, Denmark: e-mail: [email protected] Matysik, M., 2016. Facies types and depositional environments of a morphologically diverse carbonate platform: a case study from the Muschelkalk (Middle Triassic) of Upper Silesia, southern Poland. Annales Societatis Geolo- gorum Poloniae, 86: 119-164. Abstract: The detailed sedimentological study of the 150-m-thick Muschelkalk succession, deposited on a small (~200 by 80 km), morphologically diverse Upper Silesian carbonate platform during four major marine-trans- gressive pulses of the Tethys Ocean, enhanced the understanding of the depositional history, palaeogeography, and facies distribution. A total of thirty-five lithofacies types were identified, described and interpreted in terms of depositional settings. These different lithofacies represent various shallow-marine environments along the plat form transect, from peritidal to offshore areas. The vertical and lateral organization of the lithofacies delineated was caused by the interplay of platform morphology, third-order eustasy and the long-term tectonic evolution of the area. Accordingly, the carbonate system studied is a good example of the influence of large-scale processes on the facies architecture of carbonate platforms. In general, all of the four Transgressive Systems Tracts are charac terized by similarity in lithofacies composition and vertical succession and by minor lateral change, indicating only limited influence of the three large-scale factors mentioned on lithofacies development and distribution during transgressions. -
A New Large Capitosaurid Temnospondyl Amphibian from the Early Triassic of Poland
A new large capitosaurid temnospondyl amphibian from the Early Triassic of Poland TOMASZ SULEJ and GRZEGORZ NIEDŹWIEDZKI Sulej, T. and Niedźwiedzki, G. 2013. A new large capitosaurid temnospondyl amphibian from the Early Triassic of Po− land. Acta Palaeontologica Polonica 58 (1): 65–75. The Early Triassic record of the large capitosaurid amphibian genus Parotosuchus is supplemented by new material from fluvial deposits of Wióry, southern Poland, corresponding in age to the Detfurth Formation (Spathian, Late Olenekian) of the Germanic Basin. The skull of the new capitosaurid shows an “intermediate” morphology between that of Paroto− suchus helgolandicus from the Volpriehausen−Detfurth Formation (Smithian, Early Olenekian) of Germany and the slightly younger Parotosuchus orenburgensis from European Russia. These three species may represent an evolutionary lineage that underwent a progressive shifting of the jaw articulation anteriorly. The morphology of the Polish form is dis− tinct enough from other species of Parotosuchus to warrant erection of a new species. The very large mandible of Parot− osuchus ptaszynskii sp. nov. indicates that this was one of the largest tetrapod of the Early Triassic. Its prominent anatomi− cal features include a triangular retroarticular process and an elongated base of the hamate process. Key words: Temnospondyli, Capitosauridae, Buntsandstein, Spathian, Olenekian, Triassic, Holy Cross Mountains, Poland. Tomasz Sulej [[email protected]], Institute of Paleobiology, Polish Academy of Sciences, ul. Twarda 51/55, PL−00−818 Warszawa, Poland; Grzegorz Niedźwiedzki [[email protected]], Institute of Paleobiology, Polish Academy of Sciences, ul. Twarda 51/55, PL−00−818 Warszawa, Poland; current addresses: Department of Organismal Biology, Uppsala Uni− versity, Norbyvägen 18A, 752 36 Uppsala, Sweden and Department of Paleobiology and Evolution, Faculty of Biology, University of Warsaw, ul.