Abstract:A new and precisely defined chronometric subdivision of the Badenian (Middle Miocene, regional stage of Central Paratethys) is proposed. This uses global events, mainly geomagnetic polarity reversals as correlated chronometric boundaries, supported by climatic and sea-level changes in addition to isotope events and biostratigraphic data. The Karpatian/ Badenian boundary lies at 16.303 Ma, at the top of Chron C5Cn.2n, which is near the base of the Praeorbulina sicana Lowest-occurrence Zone (LOZ). The Badenian/Sarmatian boundary is placed at the top of polarity Chron C5Ar.2n, thus at 12.829 Ma. In relation to three sea level cycles TB 2.3, TB 2.4 and TB 2.5 and astronomically confirmed data, the Badenian can be divided into three parts of nearly equivalent duration. The Early Badenian as newly defined here ranges from 16.303 to 15.032 Ma (top of polarity Chron C5Bn.2n). The younger boundary correlates roughly to the base of the planktonic foraminifera Orbulina suturalis LOZ at 15.10 Ma, the HO (Highest Occurrence) of the nannofossil Helicosphaera ampliaperta at 14.91 Ma (NN4/NN5 boundary) and the Lan2/Ser1 sequence boundary at 14.80 Ma. The subsequent Mid Badenian ranges from 15.032 Ma to 13.82 Ma; the latter datum correlates with the base of the Serravallian, characterized by a strong global cooling event reflected in the oxygen isotope event Mi3b. The main part of cycle TB 2.4 falls into the Mid Badenian, which can be subdivided by a short cooling event at 14.24 Ma during the Middle Miocene Climate Transition (14.70 to 13.82 Ma). The HCO (Highest common occurrence) of the nannofossil Helicosphaera waltrans at 14.357 Ma supports this division, also seen in the tropical plankton Zones M6 Orbulina suturalis LOZ and M7 Fohsella peripheroacuta LOZ that correspond roughly to the lower and upper Lagenidae zones in the Vienna Basin, respectively. The Late Badenian is delimited in time at the base to 13.82 Ma by the Langhian/Serravallian boundary and at the top by the top of polarity Chron C5Ar.2n at 12.829 Ma. The Mediterranean Langhian/Serravallian boundary can be equated with the Mid/Late Badenian boundary at 13.82 Ma. However, the Karpatian/Badenian boundary at 16.303 Ma, a significant event easily recognizable in biostratigraphy, paleoclimate evolution and sequence stratigraphy, cannot be equated with the proposed global Burdigalian/Langhian, and thus Early/Middle Miocene boundary, at 15.974 Ma.

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Reconstruction of fossil teleost faunas can provide important information on palaeoenvironments, palaeogeography and evolution, and otoliths are particularly useful for that purpose. Here we present an otolith-

Oligocene and Lower Miocene deposits in the Paratethys are important source rocks, but reveal major stratigraphic and regional differences. As a consequence of the first Paratethys isolation, source rocks with very good oil potential accumulated during Early Oligocene time in the Central Paratethys. Coeval source rocks in the Eastern Paratethys are characterized by a lower source potential. With the exception of the Carpathian Basin and the eastern Kura Basin, the source potential of Upper Oligocene and Lower Miocene units is low. In general, this is also valid for rocks formed during the second (Kozakhurian) isolation of the Eastern Paratethys. However, upwelling along a shelf-break canyon caused deposition of prolific diatomaceous source rocks in the western Black Sea.Overall, Oligocene–Lower Miocene sediments in the Carpathian Basin (Menilite Formation) can generate up to 10 t HC m−2. Its high petroleum potential is a consequence of the interplay of very high productivity of siliceous organisms and excellent preservation in a deep silled basin. In contrast, the petroleum potential of Oligocene–Lower Miocene (Maikopian) sediments in the Eastern Paratethys is surprisingly low (often <2 t HC m−2). It is, therefore, questionable whether these sediments are the only source rocks in the Eastern Paratethys.

Life and depositional environments in the sublittoral zone of Lake Pannon, a large, brackish Paratethyan lake from the Late Miocene, were reconstructed from fossils and facies of the Szák Formation. This formation is exposed in several, roughly coeval (9.4-8.9 Ma) outcrops, located along strike of the paleo-shelf-break in northwestern Hungary. The silty argillaceous marl of the formation was deposited below storm wave base, at 20-30 to 80-90 m water depth. The abundance of benthic organisms indicates that the bottom water was usually well oxygenated. Interstitial dysoxia, however, may have occurred immediately below the sediment-water interface, as evidenced by occasional preservation of trace fossils such as Diplocraterion. The fauna comprised endemic mollusks, including brackish cockles of the subfamily Lymnocardiinae, dreissenid mussels (Congeria), and highly adapted, uniquely large-sized deep-water pulmonate snails (planorbids and lymnaeids). Ostracods were dominated by endemic species and, in some cases, endemic genera of candonids, leptocytherids, cypridids, and loxoconchids. Fish remnants include a sciaenid otolith and the oldest skeletal occurrence of Perca in Europe. The phytoplankton comprised exclusively endemic coccolithophorids, mostly endemic dinoflagellates (prevailingly Spiniferites), and cosmopolitan green algae. The Late Miocene fauna and flora of Lake Pannon were in many ways similar to the modern Caspian biota, and in particular cases can be regarded as its precursor.