Flora of the Kazanian–Urzhumian boundary in the middle Permian of the Russian Platform

Rich fossil plant localities in the upper Guadalupian and the lowermost Lopingian of the Russian Platform are confined to several discrete “levels” or “horizons” divided by intervals that are almost devoid of plant remains. One such “horizon” is located at the boundary between the Upper Kazanian and the Urzhumian of the regional stratigraphic scale. Numerous localities of this level can be grouped into two geographical clusters, the northern one being confined to the Kama River Basin, and the southern one to the Orenburg Region and Southern Bashkortostan. Regarding the southern localities, three floras that are seemingly successive in time can be distinguished. Against a common background of articulates (Paracalamites and Equisetites), the lowermost flora is characterized by the dominance of leaves of Rufloria (Cordaitanthales) with very rare conifers. Conifers (Quadrocladus, Sashinia, Dvinostrobus) and leaves of Phylladoderma (Peltaspermales) are the most abundant elements of the middle assemblage, whereas Rufloria leaves are very seldom found together with the peltasperm Ginkgophyllum and the conifer-like Steirophyllum. The uppermost flora is dominated by Odontopteridium and Ustyugia, two closely related genera of peltasperms, whereas cordaitaleans are totally absent. Comparison with the northern localities, which can be linked to the type sections of the Upper Kazanian and the Urzhumian, enables the dating of these assemblages in terms of the regional stratigraphic scale. All three floras prove to be confined to the uppermost Kazanian, and only the youngest one could also occur in the lowermost Urzhumian. As the stratigraphic ranges of all observed plant taxa exceed the total stratigraphic interval under study, the sequence of the floras seems to be caused by ecological (most likely climatic) factors rather than the actual evolution of plants. In particular, the observed gradual elimination of cordaitaleans confirms the general view on the extinction of this group on the Russian Platform. The southwestern boundary of the occurrence of cordaitaleans on the Russian Platform stretched from the southwest to the northeast, approximately parallel to the palaeolatitudes reconstructed on the basis of palaeomagnetic data. During the Guadalupian it moved to the northeast, which is to the north considering the position of the North Pole of that time. Cordaitaleans were the main peat-forming plants in the Late Palaeozoic of northern Pangea (in the Kuznetsk, Tunguska and Pechora Basins). So their retreat to the north was most likely a consequence and a reflection of the warming and drying of the climate.     

Stromatolite-dominated microbialites at the Permian–Triassic boundary of the Xikou section on South Qinling Block,China

Permian–Triassic boundary microbialites (PTBMs) are organosedimentary carbonates formed immediately after the end-Permian mass extinction. All those reported PTBMs constrained by convincing conodont biozones are present stratigraphycally not higher than the Hindeodus parvus zone and most of them are dominated by thrombolites. This paper provides the first record of a brief, but spectacular development of stromatolite-dominated PTBMs within the basal Isarcicella isarcica conodont zone of the earliest Triassic from the Xikou section of South Qinling Block that was at the margin of the North China Block during the Permian–Triassic transition and was geographically separated from the major occurrence of post-extinction microbialites in the South China Block. This stromatolite cap overlies a 3.7-m-thick oolitic limestone and is composed of a lower 0.2-m-thick bed and an upper 0.5-m-thick bed, separated by a 0.2-m-thick greyish green siliciclastic mudstone. These two stromatolite beds mainly consist of columnar stromatolites with subordinate domal stromatolites. The intercolumn and interstitial spaces within the stromatolites are filled with oolitic grainstones. At the microscopic scale, laminoid structures in stromatolites comprise wavy, millimetric-domical and tangled laminae. The increased grain and fossil contents and/or bioturbation in the domical and tangled laminae indicate that the formation of these laminae is likely related to an increase in the populations and the disruptions by benthic metazoans, as well as an influx of sediment grains. The δ¹³C_carb values fluctuate between 2‰ and 3‰ in the uppermost Permian strata; a distinct negative shift of 1.9‰ occurs at the topmost oolitic grainstone, just below the lower stromatolite bed, and the lowest value of −0.1‰ is located at the base of the upper stromatolite bed. The stratigraphic succession from stromatolites to thrombolites of the PTBMs may represent a transgressive succession and/or a transient ecosystem recovery immediately after the end-Permian mass extinction. The thrombolites-dominated PTBMs mainly developed in near-equator shallow marine geographic locations, and stromatolite-dominated PTBMs mainly developed at higher latitude settings, which probably indicates that a relatively lower diversity and abundance of marine benthic metazoans existed at higher latitudes after the end-Permian mass extinction.     

Microbialite concretions in a dolostone crust at the Permian–Triassic boundary of the Xishan section in Jiangsu Province,South China

Carbonate concretions with structures and fossil groups associated with microbialite developed in a dolostone crust at the Permian–Triassic boundary of the Xishan section in Jiangsu Province, South China. These structures include clotted fabrics and laminated carbonate needles, as well as abundant carbonate crystal fans. Fossil groups associated with microbialite include microconchids, small gastropods, and small foraminifers. These fabrics and fossils suggest that the concretions are carbonate microbialite blocks developed in the dolostone crust. On the basis of the analysis of the microfabrics and the fossil groups together with a comparison to modern analogues, we attribute the formation of the micritic patches in the microbialite concretions to the calcification of cyanobacterial mats via carbonate nanoparticles and we attribute the carbonate crystal fans to the direct recrystallization of micritic carbonates. The sparitic patches were interpreted as either the direct recrystallization of micritic carbonates or the precipitation of carbonate spars in the inter-/intra-spaces of metazoan shells together with the recrystallization of these shells. The similarities to modern stromatolites, both in morphology and in internal texture, suggest that the laminated carbonate needles are stromatolite laminae built by filamentous cyanobacteria. The preservation of these microbialite microfabrics indicates that early lithification by carbonate precipitation was widespread and intense following the end-Permian boundary events. The weak development of microbialites as small concretions may be attributed to the deeper water depth and the lower water energy in the Xishan area during the earliest Triassic.     

Sequence of Permian Tetrapod Faunas of Eastern Europe and the Permian–Triassic Ecological Crisis

Eastern Europe shows the most complete in the world continuous sequence of continental Permian and Triassic deposits, which allows the development of tetrapod faunas over more than 17 successive stages to be traced. The newly obtained data on transitional Vyazniki and Sundyr tetrapod faunas provide more complete characteristics of the Severodvinian (Late Guadalupian, pre-Lopingian) and Permian-Triassic ecological crises and the ways of replacement of the dominant vertebrate groups of Eastern Europe.     

Permian and early Triassic isotopic records of carbon and strontium in Australia and a scenario of events about the Permian‐Triassic boundary

The negative shift in δ¹³C values of carbonate carbon at the Permian/Triassic boundary is one of the better documented geochemical signatures of a mass extinction event. The similar negative shift in δ¹³C values in organic carbon from Permian/Triassic boundary marine sediments in Austria and Canada is shown to occur also in marine and non‐marine sediments from Australian sedimentary basins. This negative shift in δ¹³C values is used to calibrate Australian sections lacking diagnostic faunal elements identifying the Permian/Triassic boundary. The minimum in the carbonate ⁸⁷Sr/⁸⁶Sr seawater curve from carbonates across the Guadalupian/Ochoan Stage boundary, mainly from North America, is shown to occur also in brachiopod calcite mainly from the Bowen Basin of eastern Australia, hence providing a second calibration point in the Australian sedimentary record. These two geochemical events support a model of a runaway greenhouse developing about the Permian/Triassic boundary; this is inferred to have contributed to the end‐Permian mass extinction.     

Terrestrial Ecology around the Permian–Triassic Boundary

Permian–Triassic event is usually regarded as the greatest mass extinction in the Earth’s history, although detailed studies have shown that it was not very severe. Localities of fossil insects in European Russia, Tunguska and Kuznetsk basins, and Mongolia provide a unique (the best in the world) opportunity to study the preparation, course of the crisis, and restoration of the biota after it. It is generally believed that climatic changes causing the crisis resulted from eruption of the Siberian traps, so that localities of intertrappean deposits were undoubtedly formed during the crisis. Sedimentation conditions of volcanogenic deposits provide the most detailed time resolution, so that the crisis processes can be investigated in detail. The dynamics of insect diversity in the Paleozoic and basal Mesozoic shows that mass extinctions were absent, although many groups disappeared for some time from the taphonomic window. The crisis events in ecosystems appear earlier than events usually considered as the reason for crisis. The analysis of oryctocoenoses from localities of the intertrappean beds has shown that, during the formation of traps on the mountain plateau, rather diverse ecosystems were retained, including those of the forest formations. They are a source of information, allowing restoration of ecosystems at the end of the Early Triassic.     

Facies and diagenetic evaluation of the Permian–Triassic boundary interval and basal Triassic carbonates: shallow and deep ramp sections,Hungary

The Permian–Triassic boundary and basal Triassic shallow-marine successions were studied and correlated in sections of two structural units in Hungary (Transdanubian Range and Bükk units). Core sections in the Transdanubian Range unit recovered inner ramp deposits whereas outcrops in the Bükk unit expose deposits of the deeper ramp area of the western Tethys. The inner ramp section (studied ca. 10 m in thickness) is characterized by a succession of dolomites overlain by bioclastic limestones, peloidal grainstones (which recorded the biotic decline) and oolites with finely crystalline limestone interlayers. The deeper ramp section (studied ca. 15 m in thickness) is characterized by a succession of bioclastic limestones and marlstones, mudstone beds (recording the first biotic decline), the ‘boundary shales’ (recording the second biotic decline and the stable carbon isotope marker), mudstones with wackestone laminae, and stromatolite boundstones. Accordingly, oolite formation and microbial micrite precipitation represent carbonate sedimentary responses of end-Permian mass extinction on the carbonate shelf. In both successions, mudstones predominate the upsection, suggesting a relative sea-level rise. The succession of the deep ramp area exhibits a continuous sediment accumulation and the diagenesis here was influenced by marine and marine-derived pore water. The δ¹³C curve shows a continuous change towards more negative values, starting in bioclastic limestones, followed by a sharp symmetric negative peak at the second biotic decline that is a chemostratigraphic marker of the boundary event. Facies and microfacies trend of the inner ramp carbonates in the Transdanubian Range unit exhibits close similarities to that found in many South Alpine sections. Relict peloidal deposits, formed cemented submarine hardground substrate, indicate the extinction level. Sedimentary and diagenetic features of the overlying oolite bedset revealed slightly different depositional environments in the two studied Transdanubian Range unit sections. Petrography of the oolites highlighted shallow burial diagenetic alterations which includes marine cementation, marine-burial replacement and dolomitization. A lack of the specific negative peak in the δ¹³C values is most likely due to the multiple redeposition events of the sedimentary grains. This led to the conclusion that the deeper ramp deposits (e.g., in Bükk unit) have greater potential for recognizing trends in processes, affecting the marine environments and related to the end-Permian mass extinction, at the western Tethys.     

Lower–middle Frasnian organic carbon isotope record of conodonts in East European Platform

The early–middle Frasnian boundary interval of the northern part of the East European Platform (northwest of Russia) corresponding to the transitans-punctata isotope event is revealed by biostratigraphically constrained conodont carbon stable isotope data (δ¹³C_con). The dynamics of δ¹³C_con demonstrate a three-fold pattern with positive peaks at the onset of the main phase of the transitans-punctata isotope event (upper part of Montagne Noire 4 conodont Zone, MN4; up to -22.5‰ VPDB), and during the late part of the event (lower and middle parts of MN6 Zone; up to -24.0‰ VPDB and -22.1‰ VPDB). The stratigraphic level near the MN5 and MN6 boundary is marked by a prominent negative excursion in δ¹³C_con (down to -31.8‰ VPDB) that resembles the negative excursion in the terminal phase of the transitans-punctata isotope event worldwide. The δ¹³C_con variations in different taxa are generally consistent but demonstrate some differences in values and amplitudes. It is assumed that variations in the carbon isotopic compositions of conodonts were mainly controlled by changes in the isotope composition of the planktons as the main food source for conodonts.     

Ostracod recovery in the aftermath of the Permian–Triassic crisis: Palaeozoic–Mesozoic turnover

Results of a detailed bathymetric survey of Crater Lake conducted in 2000, combined with previous results of submersible and dredge sampling, form the basis for a geologic map of the lake floor and a model for the filling of Crater Lake with water. The most prominent landforms beneath the surface of Crater Lake are andesite volcanoes that were active as the lake was filling with water, following caldera collapse during the climactic eruption of Mount Mazama 7700 cal. yr B.P. The Wizard Island volcano is the largest and probably was active longest, ceasing eruptions when the lake was 80 m lower than present. East of Wizard Island is the central platform volcano and related lava flow fields on the caldera floor. Merriam Cone is a symmetrical andesitic volcano that apparently was constructed subaqueously during the same period as the Wizard Island and central platform volcanoes. The youngest postcaldera volcanic feature is a small rhyodacite dome on the east flank of the Wizard Island edifice that dates from 4800 cal. yr B.P. The bathymetry also yields information on bedrock outcrops and talus/debris slopes of the caldera walls. Gravity flows transport sediment from wall sources to the deep basins of the lake. Several debris-avalanche deposits, containing blocks up to 280 m long, are present on the caldera floor and occur below major embayments in the caldera walls. Geothermal phenomena on the lake floor are bacterial mats, pools of solute-rich warm water, and fossil subaqueous hot spring deposits. Lake level is maintained by a balance between precipitation and inflow versus evaporation and leakage. High-resolution bathymetry reveals a series of up to nine drowned beaches in the upper 30 m of the lake that we propose reflect stillstands subsequent to filling of Crater Lake. A prominent wave-cut platform between 4 m depth and present lake level that commonly is up to 40 m wide suggests that the surface of Crater Lake has been at this elevation for a very long time. Lake level apparently is limited by leakage through a permeable layer in the northeast caldera wall. The deepest drowned beach approximately corresponds to the base of the permeable layer. Among a group of lake filling models, our preferred one is constrained by the drowned beaches, the permeable layer in the caldera wall, and paleoclimatic data. We used a precipitation rate 70% of modern as a limiting case. Satisfactory models require leakage to be proportional to elevation and the best fit model has a linear combination of 45% leakage proportional to elevation and 55% of leakage proportional to elevation above the base of the permeable layer. At modern precipitation rates, the lake would have taken 420 yr to fill, or a maximum of 740 yr if precipitation was 70% of the modern value. The filling model provides a chronology for prehistoric passage zones on postcaldera volcanoes that ceased erupting before the lake was filled.     

Proteromorphosis of Neospathodus (Conodonta) during the Permian–Triassic crisis and recovery

The Permian–Triassic evolution of platform conodonts (Gondolellidae) consists mainly of the development of the carina and the platform. During the sublethal environmental stress conditions subsequent to the Permian–Triassic extinction, the Wuchiapingian–Griesbachian Clarkina lineage is replaced by the primitive looking platform-lacking Dienerian–Aegean Neospathodus kummeli–Kashmirella timorensis lineage. It is assumed that, above Jinogondolella denticulata, end of the Capitanian Jinogondolella lineage, “Neospathodus” arcucristatus, an atavistic blade-like homeomorph that lacks a platform, underlies Protoclarkina crofti, of the base of the anagenetic Clarkina lineage. These primitive-looking forms are derived from their immediate ancestors by retrograde evolution, a phenomenon that has been described as proteromorphosis. Such events suggest that proteromorphosis occurs during periods of crisis, with the sudden reappearance of homeomorphic forms that are atavistic representatives of the clade. The phenomenon is further substantiated by several additional retrogradations that pace the Triassic, a period prone to such events.     

The Permian–Triassic transition and the onset of Mesozoic sedimentation at the northwestern peri-Tethyan domain scale: Palaeogeographic maps and geodynamic implications

The main aim of this paper is to review Middle Permian through Middle Triassic continental successions in European. Secondly, areas of Middle–Late Permian sedimentation, the Permian–Triassic Boundary (PTB) and the onset of Triassic sedimentation at the scale of the westernmost peri-Tethyan domain are defined in order to construct palaeogeographic maps of the area and to discuss the impact of tectonics, climate and sediment supply on the preservation of continental sediment.At the scale of the western European peri-Tethyan basins, the Upper Permian is characterised by a general progradational pattern from playa-lake or floodplain to fluvial environments. In the northern Variscan Belt domain, areas of sedimentation were either isolated or connected to the large basin, which was occupied by the Zechstein Sea. In the southern Variscan Belt, during the Late Permian, either isolated endoreic basins occurred, with palaeocurrent directions indicating local sources, or basins underwent erosion and/or there was no deposition. These basins were not connected with the Tethys Ocean, which could be explained by a high border formed by Corsica–Sardinia palaeorelief and even parts of the Kabilia microplate. The palaeoflora and sedimentary environments suggest warm and semi-arid climatic conditions.At the scale of the whole study area, an unconformity (more or less angular) is observed almost everywhere between deposits of the Upper Permian and Triassic, except in the central part of the Germanic Basin. The sedimentation gap is more developed in the southern area where, in some basins, Upper Permian sediment does not occur. The large sedimentary supply, erosion and/or lack of deposition during the Late Permian, as well as the variable palaeocurrent direction pattern between the Middle–Late Permian and the Early Triassic indicate a period of relief rejuvenation during the Late Permian. During the Induan, all the intra-belt basins were under erosion and sediment was only preserved in the extra-belt domains (the northern and extreme southern domains). In the northern domain (the central part of the Germanic Basin), sediment was preserved under the same climatic conditions as during the latest Permian, whereas in the extreme southern domain, it was probably preserved in the Tethys Ocean, implying a large amount of detrital components entering the marine waters. Mesozoic sedimentation began in the early Olenekian; the ephemeral fluvial systems indicate arid climatic conditions during this period. Three distinct areas of sedimentation occur: a northern and southern domain, separated by an intra-belt domain. The latter accumulated sediments during the Early–Middle Permian and experienced erosion and/or no-deposition conditions between the Middle–Late Permian and the beginning of Mesozoic sedimentation, dated as Anisian to Hettangian. At the top of the Lower Triassic, another tectonically induced, more or less angular unconformity is observed: the Hardegsen unconformity, which is dated as intra-Spathian and is especially found in the North European basins. This tectonic activity created new source areas and a new fluvial style, with marine influences at the distal part of the systems. During the Anisian and Ladinian, continental sedimentation was characterised by a retrogradational trend. In other words, the fluvial system evolved into fluvio-marine environments, attesting to a direct influence of the Tethys Ocean in the southern and northern domains. Both at the end of the Olenekian (Spathian) and during the Anisian, the presence of palaeosols, micro- and macrofloras indicate less arid conditions throughout this domain.     

Migration patterns of the Osprey Pandion haliaetus on the Eastern European–East African flyway

We analysed migration strategies of the Osprey Pandion haliaetus on the poorly studied Eastern European–East African flyway. Four adult birds were equipped with GPS-based satellite-transmitters or data-loggers in their breeding sites in Estonia (north-eastern Europe) and tracked to their wintering grounds in Africa and back, during up to six migration cycles. Departure times, migration routes, as well as wintering and stopover sites varied remarkably between individuals but not much between years. Stopovers (2–30 days) were made mostly in Europe and less in the Middle East (Turkey) and north-eastern Africa (Egypt). The Ospreys did not avoid flying long distances over the sea, and the sea was crossed four times during the night. The current study adds to current knowledge on Osprey migration and should help to concentrate actions on protecting important flyways and stopover locations.     

Reinvestigation of conchostracans (Crustacea: Branchiopoda) from the Permian–Triassic transition in Southwest China

Sedimentary deposits of the Permian–Triassic transition are well-exposed in numerous outcrops of South China. Depending on the palaeogeographic positions of the sections, their lithofacies vary from fully marine, shallow marine, lagoonal, lacustrine, and fluvial to alluvial. In the present study, conchostracans (Crustacea: Branchiopoda) were newly collected from the continental deposits of the Kayitou and Jialingjiang formations around the Kangdian Highland elevated by the Emeishan Basalt in the southern Sichuan, western Guizhou, and northeastern Yunnan provinces. The conchostracan fauna of the Kayitou Formation is composed of Pseudestheria chatangensis, Euestheria fuyuanensis, and Euestheria sp. aff. E. gutta. These species occur in varying lithofacies types of different sections. In particular, the late Permian Pseudestheria chatangensis occurs in grey siltstones interbedded with pebbly sandstones, which are interpreted as lacustrine deposits. Euestheria fuyuanensis and Euestheria sp. aff. E. gutta were obtained from yellowish to greenish–grey clay- and siltstones, interpreted as coastal plain deposits. In comparison to other regions, occurrences of Euestheria gutta are indicative of an early Induan to Olenekian (Early Triassic) age. The fossil record of Euestheria fuyuanensis is so far restricted to a few occurrences in the Kayitou Formation of Southwest China and, therefore, using this species for long-distance biostratigraphic correlation requires further investigation. The distribution of late Permian pseudestheriid and Early Triassic euestheriid species in the respective sections possibly depends on the local lithofacies and, therefore, a diachronous age of the Kayitou Formation within the study area can be assumed. Additionally, Magniestheria sp. aff. M. mangaliensis and Magniestheria sp. aff. M. subcircularis were recorded in the Jialingjiang Formation, which represents a lithostratigraphic unit considered as late Early Triassic (Olenekian). Further investigations of both taxonomy and the real stratigraphic ranges of the conchostracan species as well as cross-correlations with other age data are recommended, in order to better constrain the position of the Permian–Triassic boundary and the specific timing of the terrestrial end-Permian mass extinction in continental deposits of Southwest China.     

Lithostratigraphy and carbonate microfacies across the Permian–Triassic boundary near Julfa (NW Iran) and in the Baghuk Mountains (Central Iran)

Permian–Triassic boundary sections in the Julfa (NW Iran) and Abadeh (Central Iran) regions display a succession of three characteristic rock units, (1) the Paratirolites Limestone with the mass extinction horizon at its top, (2) the ‘Boundary Clay’, and (3) the earliest Triassic Elikah Formation with the conodont P–Tr boundary at its base. The carbonate microfacies reveals a facies change, in the sections near Julfa, within the Paratirolites Limestone with an increasing number of intraclasts, Fe–Mn crusts, and biogenic encrustation. A decline in carbonate accumulation occurs towards the top of the unit with a sponge packstone in the sections, and finally resulting in a complete demise of the carbonate factory. The succession of the ‘Boundary Clay’ differs in the two regions; thin horizons of sponge packstone are present in the Julfa region and ‘calcite fans’ of probably inorganic origin in the Abadeh Region. The skeletal carbonate factory of the Late Permian was restored with the deposition of microbial carbonates at the base of the Elikah Formation, where densely laminated bindstone, floatstone with sparry calcite spheres, and oncoid wackestone/floatstone predominate.     

The palynological assemblages from the J–K boundary beds of the Bureya Basin,Russian Far East

Palynological assemblages were studied from the coal-bearing Upper Jurassic (Talanja Formation) to the Lower Cretaceous (Dublikan Formation) deposits of the Bureya Basin, Russia. The palynological assemblages from the upper part of the Talanja Formation are dominated by gymnosperms, mainly Ginkgocycadophytus (up to 40%) and conifers related to Pinaceae (up to 70%). The contribution of non-seed plants is not great, but their diversity is considerable. The miospore assemblages of the Talanja sequence are characterized by the last appearance of the spore taxa Staplinisporites pocockii, Camptotriletes cerebriformis, Camptotriletes nitida, and Cingulatisporites sanguinolentus. The palynological assemblage from the Dublikan Formation is dominated by ferns (up to 84%), represented mainly by Cyathidites and Duplexisporites. Among gymnosperms the role of Classopollis increases (making up about 20%). Another feature is the first appearance of the spore taxa Stereisporites bujargiensis, Neoraistrickia rotundiformis, Contignisporites dorsostriatus, Appendicisporites tricostatus, and Concavissimisporites asper.     

The Cenomanian–Turonian boundary in the northwestern part of the Adriatic Carbonate Platform (Ćićarija Mtn., Istria,Croatia): characteristics and implications

The Cenomanian–Turonian boundary (CTB) in the ?i?arija Mountain region (northern Istria, Croatia) is characterized by calcisphere limestone successions with a firmground and glauconite horizon, bioturbated intervals, tempestites, and slumped structures as well as microbially laminated and organic-rich interbeds deposited in the northwestern part of the intra-Tethyan Adriatic Carbonate Platform (AdCP). Compilation of the results from three studied sections (Vodice–Jelovica, Martinjak and Planik) of litho-, bio-, and microfacies analyses, X-ray diffraction, SEM, EDS, and stable isotope analyses allowed reconstruction of marine paleoenvironmental conditions during this time period. Shallow-marine carbonate deposits of the Milna Formation underlie a drowned-platform succession of the Sveti (Sv.) Duh Formation. The contact between these two formations is sharp and commonly marked by slumped deposits. The Sv. Duh Formation consists of about 100 m of calcisphere wackestone enriched in organic matter. The results of preliminary δ¹³C and δ¹⁸O stable isotope analyses indicate the influence of the global Oceanic Anoxic Event (OAE2) on the deposition of this carbonate succession. Anoxic and hypoxic conditions in the water column lead to major changes in the shallow-marine carbonate system of the AdCP. Numerous benthic foraminifera declined during that time, but planktonic foraminifera and calcareous dinoflagellates diversified and expanded greatly. The results of this research provide new insights into the character of the CTB interval in this part of the Tethyan realm. Local and regional synsedimentary tectonics combined with global upper Cretaceous sea-level dynamics allows the correlation of the investigated deeper-marine lithostratigraphic units with OAE2.