Szabó János szerk.: Fragmenta Mineralogica Et Palaentologica 21. 2003. (Budapest, 2003)

Beside these main ontogentic and phylogeneric regulari­ties several more connections and relationships have been revealed by studies discussed in this paper. The more important ones are the following. — In every lineage, the evolution resulted in two kinds of components, namely: progressive and regressive elements. Progressive elements are: more and more compact spire, larger chambers, increase in the diameter of the shell and the megasphere, thickening of the marginal lath, increase in the number of septa, complication of the suture line, appearance of granulation. Regressive elements are: loosening of the spire, increase in chamber height, decrease in the diameter of the shell and of the megasphere, and degeneration phenomena. The ratio of progressive and regressive elements defines the direction, nature and rate of evolution. The progressive ele­ments are dominating in the cases of N. perforatus, N. brongniarti and N. millecaput. They are characterized by big, even gigantic size (up to 80—100 mm), hundreds, in extreme cases thousands of chambers, and three-sectoral spire. With time, these features become overdeveloped. This, along with degeneration phenomena, resulted in parakme during the Bartonian, terminating with the extinction of the species. None of them passed the Middle/Late Eocene boundary. — The appearing new taxa evolve mainly by diver­gence, not by anagenesis. This means that an evolutionarily "plastic" (mosdy very variable) species bears in itself the general evolutionary trend of features, and new taxa are produced by the factors of evolution (spreading, shift, isolation, selection etc.). Examples: the separation of N. striatus minor, N. subtilis, N. kopeki from N. stiratus, the separation of the N. dudarensis, N. maj^oni, N. iohannis, and N. sinensis from N. variolarius. — It could be established that in the investigated fau­nas, there are numerous taxa, which have evolved under the influence of ecological and geographical factors (N. suemegensis, N. pen^esgyoerensis, N. dudarensis, N. sinensis). As a rule, the diferrence from the original taxon is not very significant. This would suggest that the populations might have been more or less interrelated. All these, as far as the Bakony Mountains region is concerned, is in connection with the temporarily and locally prevailing shallow marine influence and the environmental variability. References AIGNER, T. (1983): Facies and origin of nummuliric buildups: an example from the Giza Pyramids Plateau (Middle Eocene, Egypt). — Neues Jahrbuch für Geologic und Paläontologie, / Ibhandlungen, 166(3): 347-368. AIGNER, T. (1985): Biofabrics as dynamic indications in Nummulite accumulation. — Journal of Sedimentary Petrology, 55(1): 131-134. ARNI, P. (1965): L' évolution des Nummulitinae, en tant que facteur de modification des depots littoraux. — Mémoires Bureau Recherches Géologiques et Minieres, 32: 7—20. COPPER, P. (1988): Ecological succession in Phanerozoic reef ecosys­tems: is it real? — Palaios, 3: 136-152. DUDICH, E. JR. & MÉSZÁROS, N. (1963): Über die Verbreitung und die Typen der Krustenbewegungen und des Vulkanismus in Mittel- und Südost-Europa am Ende des Mitteleozäns. — Neues Jahrbuch für Geologie und Paläontologie, Abhandlungen, 118: 65-84. FRAGERSTROM, J. A. (1987): The evolution of reef communities. — London, Wiley Interscience: 1 —600. GRÜNIG, A. & HERB, R. (1980): Paleoecology of Late Eocene benthonic Foraminifera from Possagno (Treviso, Northern Italy). — Cushman Foundation Special Publication, Memorial to ORVILLE L. BANDY: 18: 68-85. GRÜNIG, A. & HERB, R. (1984): Eocene benthic Foraminifera from Biarritz: Distribution and Paleoenvironment. — Benthos '83; 2nd Internationale Symposium Benthic Foraminifera (Pau, April 1983): 257-265. ' HAQ, B. U., HARDENBOL, J. & VAIL, P. R. (1987): Chronology of fluctu­ating sea levels since the Triassic. — Science, 235: 1156-1167. HERB, R. (1988): Evolution of diversity, paleoenvironment and extinction in large nummulitids. — Revue de Paléolnologie, [volume spéciale], 2: 663. HILTERMANN, H. (1982): Meereskundliche und palökologische Biozönotik. — Paläontologische Zeitschrift, 56(3—4): 153—164. HILTERMANN, IT., BRÖNNLMANN, P. & ZANINETTI, L (1981): Neue Bio­zönosen in den Sedimenten der Mangrove von Acupe bei Bahia/Brasil. — Notes du Laboratoire de Paléontologie de t Université de Geneve, 8:1—6. HlLTERMANN, H. & TÜXEN, J. JR. (1974): Biosociology of recent ben­thonic Foraminifera after the Barun-Blanquet-Method. — Revista Espanola de Micropaleontologia, 6(1): 75-84. HOFFMANN, A. & KITCHELL, A. (1984): Evolution in a pelagic plancric system: a paleobiological test of models of multispecies evolution. — Paleobiology, 10: 9-33. KECSKEMÉTI, T. (1978): Paläobiogeographische Übersicht der Nummu­lites-Fauna des Bakonygebirges. — Annales historico-naturales Musei nationalis hungarici, 70: 45—59. KECSKEMÉTI, T. (1987): Contribution to the phylogeneric connections of Nummulites species. — Annales historico-naturales Musei nationalis hungarici, 79: 61-75. KECSKEMÉTI, T. (1989): Bathymétrie significance of Recent larger Fora­minifera: an example of application to the Eocene of Hungary. — Fragmenta Mineralogica et Paleontologica, 14: 73—82. KOPEKG. (1980): A Bakony hegység ÉK-i részének eocénje. L'Eocene de la partie Nord-Orientale de la Montagne du Bakony (Transdanubie, Hongrie). — A Magyar Aűamt Földiám Intézet Evkönyve, 63(1): 1-176. PAVLOVEC, R. (1983): Paleoecology of Nummulites. — Bolletino della Società Paleontologica Italiana, 22 (1-2): 15—19. ROLLINS, H. B., CAROTHERS, M. & DONAHUE, J. (1979): Transgression, regression and fossil community succession. — Lethaia, 12: 98—104. SERRA-KIEL, J. & REGLANT, S. (1984): Paleoecological conditions and morphological variation in monospecific banks of Nummulites: an example. — Benthos '83, 2nd Internationale Symposium Benthic Foraminifera (Pau, April 1983): 557-563. VlTÁLIS-ZlLAHY, L. (1963): Phylogeny of Heterostegininae (Forami­nifera) and pathological changes in Operculineila species. — Acta IMologica Hungarica, 14: 33-43. Author's address: Dr. Tibor KECSKEMÉTI Geological and Palaeontological Department Hungarian Natural History Museum Budapest, Múzeum krt. 14—16 Mail: 1431 Budapest, pf. 137 Hungary e-mail: kecs@paleo.nhmus.hu

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