The Late Jurassic to Early Cretaceous Tendaguru Beds (Tanzania, East Africa) have been well known for nearly a century for their diverse dinosaur assemblages. Here, we present sedimentological and palaeontological data collected by the German-Tanzanian Tendaguru Expedition 2000 in an attempt to reconstruct the palaeo-ecosystems of the Tendaguru Beds at their type locality. Our reconstructions are based on sedimentological data and on a palaeoecological analysis of macroinvertebrates, microvertebrates, plant fossils and microfossils (ostracods, foraminifera, charophytes, palynomorphs). In addition, we included data from previous expeditions, particularly those on the dinosaur assemblages. <br><br> The environmental model of the Tendaguru Beds presented herein comprises three broad palaeoenvironmental units in a marginal marine setting: (1) Lagoon-like, shallow marine environments above fair weather wave base and with evidence of tides and storms. These formed behind barriers such as ooid bar and siliciclastic sand bar complexes and were generally subject to minor salinity fluctuations. (2) Extended tidal flats and low-relief coastal plains. These include low-energy, brackish coastal lakes and ponds as well as pools and small fluvial channels of coastal plains in which the large dinosaurs were buried. Since these environments apparently were, at best, poorly vegetated, the main feeding grounds of giant sauropods must have been elsewhere. Presumably, tidal flats and coastal plains were visited by dinosaurs primarily during periods of drought. (3) Vegetated hinterland. Vegetation of this environment can only be inferred indirectly from plant material transported into the other depositional environments. Vegetation was dominated by a diverse conifer flora, which apparently formed part of the food source of large herbivorous sauropods. Evidence from various sources suggests a subtropical to tropical palaeoclimate, characterised by seasonal rainfall alternating with a pronounced dry season during the Late Jurassic. In Early Cretaceous times, sedimentological and palaeontological proxies suggest a climatic shift towards more humid conditions. <br><br> Die Tendaguru-Schichten von Tansania in Ostafrika (Oberjura bis Unterkreide) sind als Lagerstätte oberjurassischer Dinosaurier seit nahezu einem Jahrhundert weltweit bekannt. Anhand von sedimentologischen und paläontologischen Daten, die während der Deutsch-Tansanischen Tendaguru Expedition 2000 im Typus-Gebiet der Tendaguru-Schichten gewonnen wurden, werden Paläo-Ökosysteme rekonstruiert. Grundlage der Rekonstruktionen sind die Auswertung sedimentologischer Daten sowie die paläo-ökologische Analyse von Makroinvertebraten, Mikrovertebraten, pflanzlichen Fossilien und Mikrofossilien (Ostrakoden, Foraminiferen, Charophyten, Palynomorphen). Darüber hinaus werden Informationen über Dinosaurier berücksichtigt, die bei früheren Expeditionen gewonnen wurden. <br><br> Das hier vorgestellte Ablagerungsmodell der Tendaguru-Schichten umfaßt drei Teilbereiche eines randlich marinen Sedimentationsraumes, die wie folgt gekennzeichnet werden können: (1) Lagunen-artige, marine Flachwasserbereiche, die oberhalb der Schönwetter-Wellenbasis lagen und unter deutlichem Einfluß von Gezeiten und Stürmen standen. Sie waren vom offenen Meer durch Barrieren, wie Ooidbarren und siliziklastischen Sandbarrenkomplexen, getrennt und wiesen einen leicht schwankenden Salzgehalt auf. (2) Ausgedehnte Wattgebiete und flache Küstenebenen. Dort befanden sich niedrig-energetische, brackische Strandseen und Teiche sowie Tümpel und kleinere Flußrinnen, in denen die großen Dinosaurier eingebettet wurden. Da diese Lebensräume bestenfalls dürftig bewachsen waren, müssen die Nahrungsquellen und der eigentliche Lebensraum der riesigen Sauropoden anderswo gelegen haben. Vermutlich wurden die Wattgebiete und Flachküsten von Dinosauriern vorrangig in den Trockenzeiten aufgesucht. (3) Bewachsenes Hinterland. Die Vegetation dieses Lebensraumes kann nur indirekt aus Pflanzenresten erschlossen werden, die in die anderen Ablagerungsraume transportiert wurden. Die Vegetation wurde von einer diversen Koniferenflora dominiert, die zumindest teilweise die Nahrungsgrundlage der großen, herbivoren Sauropoden bildete. Sedimentologische und paläontologische Indikatoren sprechen für ein subtropisches bis tropisches Klima wahrend der späten Jurazeit mit einem jahreszeitlichen Wechsel von Regenfällen und ausgeprägten Trockenzeiten. In der frühen Kreidezeit deutet sich ein Wechsel zu starker humiden Bedingungen an. <br><br> doi:<a href="http://dx.doi.org/10.1002/mmng.20020050103" target="_blank">10.1002/mmng.20020050103</a>

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Amber is of great paleontological importance because it preserves a diverse array of organisms and associated remains from different habitats in and close to the amber-producing forests. Therefore, the discovery of amber inclusions is important not only for tracing the evolutionary history of lineages with otherwise poor fossil records, but also for elucidating the composition, diversity, and ecology of terrestrial paleoecosystems. Here, we report a unique find of African amber with inclusions, from the Cretaceous of Ethiopia. Ancient arthropods belonging to the ants, wasps, thrips, zorapterans, and spiders are the earliest African records of these ecologically important groups and constitute significant discoveries providing insight into the temporal and geographical origins of these lineages. Together with diverse microscopic inclusions, these findings reveal the interactions of plants, fungi and arthropods during an epoch of major change in terrestrial ecosystems, which was caused by the initial radiation of the angiosperms. Because of its age, paleogeographic location and the exceptional preservation of the inclusions, this fossil resin broadens our understanding of the ecology of Cretaceous woodlands.Arachnida | Ethiopia | Hexapoda | microorganisms | paleoecology

Abstract. Microbial life in the continental "deep biosphere" is closely linked to geodynamic processes, yet this interaction is poorly studied. The Cheb Basin in the western Eger Rift (Czech Republic) is an ideal place for such a study because it displays almost permanent seismic activity along active faults with earthquake swarms up to M L 4.5 and intense degassing of mantle-derived CO 2 in conduits that show up at the surface in form of mofettes. We hypothesize that microbial life is significantly accelerated in active fault zones and in CO 2 conduits, due to increased fluid and substrate flow. To test this hypothesis, pilot hole HJB-1 was drilled in spring 2016 at the major mofette of the Hartoušov mofette field, after extensive pre-drill surveys to optimize the well location. After drilling through a thin caprock-like structure at 78.5 m, a CO 2 blowout occurred indicating a CO 2 reservoir in the underlying sandy clay. A pumping test revealed the presence of mineral water dominated by Na + , Ca 2+ , HCO The cored sediments are mudstones with minor carbonates, sandstones and lignite coals that were deposited in a lacustrine environment. Deformation structures and alteration features are abundant in the core. Ongoing studies will show if they result from the flow of CO 2 -rich fluids or not.

The well-known Late Jurassic to Early Cretaceous Tendaguru Beds of southern Tanzania have yielded fossil plant remains, invertebrates and vertebrates, notably dinosaurs, of exceptional scientific importance. Based on data of the German-Tanzanian Tendaguru Expedition 2000 and previous studies, and in accordance with the international stratigraphic guide, we raise the Tendaguru Beds to formational rank and recognise six members (from bottom to top): Lower Dinosaur Member, Nerinella Member, Middle Dinosaur Member, Indotrigonia africana Member, Upper Dinosaur Member, and Rutitrigonia bornhardti-schwarzi Member. We characterise and discuss each member in detail in terms of derivation of name, definition of a type section, distribution, thickness, lithofacies, boundaries, palaeontology, and age. The age of the whole formation apparently ranges at least from the middle Oxfordian to the Valanginian through Hauterivian or possibly Aptian. The Tendaguru Formation constitutes a cyclic sedimentary succession, consisting of three marginal marine, sandstone-dominated depositional units and three predominantly coastal to tidal plain, fine-grained depositional units with dinosaur remains. It represents four third-order sequences, which are composed of transgressive and highstand systems tracts. Sequence boundaries are represented by transgressive ravinement surfaces and maximum flooding surfaces. In a more simple way, the depositional sequences can be subdivided into transgressive and regressive sequences/systems tracts. Whereas the transgressive systems tracts are mainly represented by shallow marine shoreface, tidal channel and sand bar sandstones, the regressive systems tracts predominantly consist of shallow tidal channel, tidal flat, and marginal lagoonal to supratidal deposits.