Climatic cyclicity and biodiversity during the Quaternary |
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The finds and data are studied by an extended international / interdisciplinary work group: |
| 1. Excavation and documentation | Teams from the Senckenberg Research Station of Quaternary Palaeontology Weimar |
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| 2. Regional and local research history | R.-D. Kahlke (Weimar) | |
| 3. Regional geology | J. Ellenberg (Jena) | |
| 4. Geology of the site | R.-D. Kahlke (Weimar) | |
| 5. Sedimentology | J. Ellenberg (Jena) | |
| 6. Palaeomagnetism | F. Wiegank (Potsdam) | |
| 7. Vegetational reconstructions | M. Stebich (Weimar), R.-D. Kahlke (Weimar) |
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| 8. Gastropods | E. Krolopp † (Budapest) | |
| 9. Fishes | R. Rutte † (Würzburg), M. Böhme (Tübingen) |
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| 10. Amphibians | G. Böhme (Berlin), M. Böhme (Tübingen) |
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| 11. Lacertilia and ophidians | M. Böhme (Tübingen) | |
| 12. Testudinates | L. C. Maul (Weimar) | |
| 13. Birds | D. Jánossy † (Budapest), J. Mlikovsky (Prague) |
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| 14. Bovids | A. Sher † (Moscow), M. Bukhsianidze (Tbilisi) |
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| 15. Cervids | H.-D. Kahlke (Weimar), M. Breda (Ferrara) |
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| 16. Hippopotamids | R.-D. Kahlke (Weimar) | |
| 17. Suids | C. Guérin (Lyon), M. Faure (Lyon) |
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| 18. Rhinocerotids | H.-D. Kahlke (Weimar), |
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| 19. Equids |
R. Musil (Brno), V. Eisenmann (Paris) |
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| 20. Elephantids | I. A. Dubrovo (Moscow), H. v. Essen (Dieren), D. Mol (Rotterdam), A. Lister (London) |
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| 21. Canids | M. V. Sotnikova (Moscow) | |
| 22. Ursids | R. Musil (Brno), N. Garcia (Madrid) |
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| 23. Mustelids | M. Wolsan (Warsaw) | |
| 24. Hyaenids | A. Turner † (Liverpool) | |
| 25. Koproliths | J.-A. Keiler (Weimar) | |
| 26. Felids | H. Hemmer (Mainz) | |
| 27. Insectivores, lagomorphs and rodents | L. C. Maul (Weimar) | |
28. Cercopithecids |
H. Zapfe † (Vienna) |
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| 29. Taphonomy | R.-D. Kahlke (Weimar), S. Gaudzinski (Neuwied) |
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| 30. Tooth root cementum analysis for determining the season of individual deaths | H. Kierdorf (Cologne), N. Garcia (Madrid) |
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| 31. Mesowear analysis | T. M. Kaiser (Hamburg) | |
| 32. Herbivore Osteophagia | R.-D. Kahlke (Weimar) | |
| 33. Rodent gnaw-marks | L. C. Maul (Weimar) | |
| 34. Palaeopathology | U. Kierdorf (Hildesheim), R.-D. Kahlke (Weimar) |
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| 35. Palaeotemperature determination | E. Stephan, H.-P. Uerpmann, B. Cramer (Tübingen) |
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| 36. Palaeoecology | R.-D. Kahlke (Weimar) | |
| 37. Stratigraphy | R.-D. Kahlke (Weimar) | |
| 38. Methods of preparation and conservation | J.-A. Keiler (Weimar) | |
| 39. Optical 3D topometry | O. Kullmer (Frankfurt/M.) | |
| 40. Analysis of stable isotopes | N. Garcia (Madrid), |
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| 41. Provenance analysis by U-Pb ages of detrital zircon | U. Linnemann (Dresden), |
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| 42. Thermoluminescence dating | M. Fuchs (Freiberg) |
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| 43. Petrography and origin of carbonates | U. Linnemann (Dresden), R.-D. Kahlke (Weimar) |
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Climatic change and orogenetic processes during the late Tertiary and Quaternary led to a drop of temperatures and humidity in Eurasia's northern and moderate latitudes. From around 500,000 yr BP, during the Middle and Late Pleistocene cold stages, the so called Mammoth Faunas (Mammuthus-Coelodonta Faunal Complex) evolved. These faunas ranked as the most effective cold-adapted mammal associations in the history of the earth.
The Eurasian cold period faunas are mostly drawn from descendents of northern tundra as well as central Asian steppe inhabitants. Studies of distribution of the fossil finds of key members of this fauna show how their geographical distributions responded to Middle and Late Pleistocene environmental changes. Moreover, the biodiversity and biogeography of the various evolutionary stages of the Pleistocene cold adapted faunas are analysed.
Associates:
D. J. Álvarez-Lao (University of Oviedo), B. Buigues (Cerpolex, Paris), N. García (University Complutense, Madrid), F. Lacombat (Musée Crozatier, Le Puy-en Velay), D. Mol (Cerpolex/Mammuthus, Amsterdam / Natuurmuseum, Rotterdam), H. v. d. Plicht (University of Groningen), J. W. F. Reumer (Natuurmuseum, Rotterdam), A. Tikhonov (Zoological Institute of the Russian Academy of Sciences, St. Petersburg)