Molluscan biostratigraphy of the Miocene and Chatt in the southern Herzogtum Lauenburg (Schleswig-Holstein)

A study was made of the marine molluscan fauna from 12 borings in the Schwarzenbek area. In the fossil rich facies underlying the 'Braunkohlensande', the Neochatt and Vierland faunal sequences could be described and used to define the Oligocene/Miocene boundary. The Neochatt, defined by Pectinidae, seems to be more closely related to the Miocene than previously thought. Nevertheless, a sufficient number of additional molluscan species are present for placing the Neochatt/Vierland boundary. Overlying the Braunkohlensande, the sandy Reinbek fauna as well as Glimmerton faunas of the Reinbek and Langenfelde stages could be described.

Fossil record of Mollusca from Neogene sediments in Schleswig-Holstein, Germany

Über die Verbreitung, Gliederung und Ausbildung des Jungtertiärs im westlichen Schleswig-Holstein war bisher nicht viel bekannt. Am besten bearbeitet sind die glazial gestauchten Schollen von Morsum/Sylt. Eine Aufzählung erbohrter Miozänvorkommen mit nicht immer überzeugender Begründung lieferte H.-L. HECK 1935. S. THIELE (1941) hat die ihm bekannten Vorkommen hauptsächlich nach faziellen und petrographischen Gesichtspunkten bearbeitet. Er erkannte richtig die Stellung der Braunkohlensande. Die angekündigte palaeontologische Bearbeitung ist nicht erschienen. Eine allgemeine Übersicht über die Entwicklung des Jungtertiärs bringen W. WOLFE und H.-L. HECK 1949. W. HINSCH lieferte wertvolle Beiträge zur Molluskenfauna und zur Gliederung des Miozäns (1952, 1955). Über neue Vorkommen von Braunkohlen-Sanden berichtete E. DITTMER(1 956), eine erste Übersicht über neue Vorkommen der Hemmoorer Stufe gab derselbe Verfasser 1957.

Eocene-Oligocene diatoms in the western Indian Ocean

The occurrence of diatom species in the Eocene-Oligocene sections of Ocean Drilling Program (ODP) Leg 115 sites and Deep Sea Drilling Project (DSDP) Sites 219 and 236 in the low-latitude Indian Ocean are investigated. Diatoms are generally rare and poorly preserved in the Paleogene sequences we studied. The best-preserved assemblages are found close to ash layers in early Oligocene sediments. The low-latitude diatom zonation established for the Atlantic region by Fenner in 1984 is fully applicable to the Paleogene sequences of the western Indian Ocean. Correlation of the diatom zones to the calcareous nannofossil stratigraphy of the sites places the Coscinodiscus excavatus Zone of Fenner within calcareous nannofossil Subzone CP16b. For the Mascarene Plateau and the Chagos Ridge, the times when the sites studied, together with the areas upslope from them, subsided to below the euphotic zone are deduced from changes in the relative abundance between the group of benthic, shallow-water species and Grammatophora spp. vs. the group of fully planktonic diatom species. The Eocene section of Site 707, on the Mascarene Plateau, is characterized by the occurrence of benthic diatoms (approximately 10% of the diatom assemblage). These allochthonous diatoms must have originated from shallow-water environments around volcanic islands that existed upslope from ODP Site 707 in Eocene times. In Oligocene and younger sediments of Sites 707 and 706, occurrences of benthic diatoms are rare and sporadic and interpreted as reworked from older sediments. This indicates that the area upslope from these two Mascarene Plateau sites had subsided below the euphotic zone by the early Oligocene. Only Grammatophora spp., for which a neritic but not benthic habitat is assumed, continues to be abundant throughout the Oligocene sequences. The area of the Madingley Rise sites (Sites 709-710) and nearby shallower areas subsided below the euphotic zone already in middle Eocene times, as benthic diatoms are almost absent from these Eocene sections. Only sites located on abyssal plains, and which intermittently received turbidite sediments (e.g., Sites 708 and 711), contain occasionally single, benthic diatoms of Oligocene age. The occurrence of the freshwater diatom Aulacosira granulata in a few samples of late early Oligocene and late Oligocene age at Sites 707, 709, and 714 is interpreted as windblown. Their presence indicates at least seasonally arid conditions for these periods in the source areas of eastern Africa and India. Three new species and two new combinations are defined: Chaetoceros asymmetricus Fenner sp. nov.; Hemiaulus gracilis Fenner, sp. nov.; Kozloviella meniscosa Fenner, sp. nov.; Cestodiscus demergitus (Fenner) Fenner comb, nov.; and Rocella princeps (Jouse) Fenner comb. nov.

Upper Turonian - lower Campanian planktonic foraminifera from Exmouth Plateau

A planktonic foraminiferal zonal scheme is presented for subdivision of the Upper Cretaceous pelagic carbonate sequence from southern mid-high latitudes. Definition of the zones is based on first and last occurrences of planktonic foraminifera from Ocean Drilling Program Holes 762C and 763B (Leg 122; Exmouth Plateau, south Indian Ocean). During the Late Cretaceous the studied holes were located close to 50°S and for the first time a complete sedimentary record for the mid-high latitudes was obtained. A detailed biostratigraphic analysis has allowed recognition of two new zones (Falsotruncana maslakovae Zone and Marginotruncana marianosi Zone) for the interval extending from the last occurrence of Helvetoglobotruncana helvetica to the first occurrence of Dicarinella asymetrica (upper Turonian - lower Santonian). From this study it is apparent that some low latitude (Globotruncana ventricosa, Hedbergella flandrini, Marginotruncana marianosi) and high latitude (Globigerinelloides impensus and Hedbergella sliteri) marker taxa display a vertical distribution at mid-high latitudes which is different from that known from low latitudes; moreover, one species (Heterohelix papula), overlooked at low latitudes, exhibits a restricted range that seems to be useful for chrono-biostratigraphic correlations: its appearance is suggested to coincide with the Coniacian/Santonian boundary. The proposed biozonation, which is integrated with calcareous nannofossil and magnetostratigraphic data available for the sections studied, is compared with both the low-latitude standard zonation and the planktonic foraminiferal zonal scheme for the circum-Antarctic region, in order to define a bio-chronostratigraphic scale that is useful for mid-high latitudes of the southern oceans.

Miocene molluscan biostratigraphy in Schleswig-Holstein, north Germany

Vierlandian, Behrendorfian (Lower Hemmoorian), Oxlundian (Upper Hemmoorian), Lower and Upper Reinbekian, Langenfeldian and Gramian stages could be proved by evaluation of marine molluscan faunas. The diachrone base of 'Braunkohlensande' is demonstrated by underlying Vierlandian mica clay in the E, and by Hemmoorian substages more to the W, at last the fluviatile facies is replaced completely by euhaline to brachyhaline sandy to silty sediments. Brachyhaline effects in adjacent environments make possible an approximate dating on fluviatile sedimentation. The widest extension of 'Braunkohlensand' is during upper Oxlundian, whilst slightly brachyhaline Katzheide beds, defined in this paper to be of Lower Reinbekian age, indicate a limit of 'Braunkohlensande' more to the E. Winnert-fauna was found to be a mixture of Oxlundian and Langenfeldian; the overlying lignitic sands belong to the Kaolinsand group. Upper mica clay overlying Miocene Braunkohlensande can be divided into beds of Upper Reinbekian, Langenfeldian and Gramian ages.

Benthic foraminifera and stable isotope record of ODP Leg 182 sites

Cores from Sites 1129, 1131, and 1132 (Ocean Drilling Program (ODP) Leg 182) on the uppermost slope at the edge of the continental shelf in the Great Australian Bight reveal the existence of upper Pleistocene bryozoan reef mounds, previously only detected on seismic lines. Benthic foraminiferal oxygen isotope data for the last 450,000 years indicate that bryozoan reef mounds predominantly accumulated during periods of lower sea level and colder climate since stage 8 at Sites 1129 and 1132 and since stage 4 at the deeper Site 1131. During glacials and interstadials (stages 2-8) the combination of lowered sea level, increased upwelling, and absence of the Leeuwin Current probably led to an enhanced carbon flux at the seafloor that favored prolific bryozoan growth and mound formation at Site 1132. At Site 1129, higher temperatures and downwelling appear to have inhibited the full development of bryozoan mounds during stages 2-4. During that time, favorable hydrographic conditions for the growth of bryozoan mounds shifted downslope from Site 1129 to Site 1131. Superimposed on these glacial-interglacial fluctuations is a distinct long-term paleoceanographic change. Prior to stage 8, benthic foraminiferal assemblages indicate low carbon flux to the seafloor, and bryozoan mounds, although present closer inshore, did not accumulate significantly at Sites 1129 and 1132, even during glacials. Our results show that the interplay of sea level change (eustatic and local, linked to platform progradation), glacial-interglacial carbon flux fluctuations (linked to local hydrographic variations), and possibly long-term climatic change strongly influenced the evolution of the Great Australian Bight carbonate margin during the late Pleistocene.