Studies of Miocene sediments in the Fore-Carpathian Basin, conducted by geologists from the University of Warsaw have provided new insights on the distribution of the facies infilling the basin, particularly in the forebulge and back-bulge zones. The origin of the large-scale sand bodies, evaporitic deposits and large-scale organic buildups is discussed, described and verified. These deposits originated in variable, shallow marine settings, differing in their water chemistry and the dynamics of sedimentary processes, and are unique with regard to the fossil assemblages they yield. Many years of taxonomic, biostratigraphic, palaeoecologic and ecotaphonomic investigations have resulted in the identification of the fossil assemblages of these sediments, their age, sedimentary settings and post-mortem conditions. Detailed studies were focused on corals, polychaetes, most classes of molluscs, crustaceans, echinoderms, and fishes.
ABSTRACT:Radwańska, U. 2017. Selected Oxfordian brachiopods from Zalas (Cracow Upland, Poland). Acta Geologica Polonica, 67 (3), 433-440. Warszawa.Small brachiopods of the families Craniidae Menke, 1828 and Thecidellinidae Elliott, 1958 were selected from the Oxfordian sequence which lies transgressively upon a Variscan rhyodacite laccolite exposed at Zalas in the Cracow Upland, southern Poland, a site which is well-known due to various kinds of ubiquitous fossils. The craniids include three species: Craniscus bipartitus (Münster in Goldfuss, 1837), Craniscus tripartitus (Münster in Goldfuss, 1837) and Craniscus antiquior (Jelly, 1843), and the thecidellinids -two species: Rioultina zalasensis sp. nov. and Rioultina wapiennensis Krawczyński, 2008. The species described herein indicate tropical or subtropical waters, and a moderately (?) deep character of the sea basin at Zalas.
The non-cidaroid echinoids (subclass Euechinoidea Bronn, 1860) from the Oxfordian epicontinental sequence of Poland (Polish Jura, Holy Cross Mountains, Mid-Polish Anticlinorium) are assigned to the genera Hemipedina Wright, 1855, Hemicidaris L. Agassiz, 1838, Hemitiaris Pomel, 1883, Pseudocidaris Étallon, 1859, Stomechinus Desor, 1856, Eucosmus L. Agassiz in Agassiz and Desor, 1846, Glypticus L. Agassiz, 1840, Pleurodiadema de Loriol, 1870, Diplopodia McCoy, 1848, Trochotiara Lambert, 1901, Desorella Cotteau, 1855, and Heterocidaris Cotteau, 1860, plus one acropeltid taxon, and one taxon left in open nomenclature. Within the genus Hemicidaris L. Agassiz, 1838, the relationship between Hemicidaris intermedia (Fleming, 1828), Hemicidaris crenularis L. Agassiz, 1839 [non Lamarck, nec Goldfuss] and Hemicidaris quenstedti Mérian, 1855, all with confused taxonomy, is discussed. Based on test structure, the genera Polydiadema Lambert, 1883, and Trochotiara Lambert, 1901, of the family Emiratiidae Ali, 1990, are proved to be separate; the common species mamillana of F.A. Roemer (1836) is a typical Trochotiara. An attention is paid to the morphology of the tiny, juvenile specimens, common in Eucosmus decoratus L. Agassiz in L. Agassiz and Desor, 1846, and in Pleurodiadema stutzi (Moesch, 1867).
Otoliths are calcium carbonate components of the stato-acoustical organ responsible for hearing and maintenance of the body balance in teleost fish. During their formation, control over, e.g., morphology and carbonate polymorph is influenced by complex insoluble collagen-like protein and soluble non-collagenous protein assemblages; many of these proteins are incorporated into their aragonite crystal structure. However, in the fossil record these proteins are considered lost through diagenetic processes, hampering studies of past biomineralization mechanisms. Here we report the presence of 11 fish-specific proteins (and several isoforms) in Miocene (ca. 14.8–14.6 Ma) phycid hake otoliths. These fossil otoliths were preserved in water-impermeable clays and exhibit microscopic and crystallographic features indistinguishable from modern representatives, consistent with an exceptionally pristine state of preservation. Indeed, these fossil otoliths retain ca. 10% of the proteins sequenced from modern counterparts, including proteins specific to inner ear development, such as otolin-1-like proteins involved in the arrangement of the otoliths into the sensory epithelium and otogelin/otogelin-like proteins that are located in the acellular membranes of the inner ear in modern fish. The specificity of these proteins excludes the possibility of external contamination. Identification of a fraction of identical proteins in modern and fossil phycid hake otoliths implies a highly conserved inner ear biomineralization process through time.
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