Palynological records of sediments from the Odderade type locality, north Germany

Reinvestigation of the Odderade Interstadial in its type locality led to an augmentation of the flora list and correction of some misinterpretations (e.g. Omorica, Frangula). The Eemian, stadials FW 1 and 3, and the interstadials Amersfoort/Broerup and Odderade have been manifested by pollen analyses. FW 1 and FW 3 are probably not completely free from forested areas. The new pollen diagrams considered with older data from Odderade, and in comparison with other regions in Central Europe, fit essentially with the classification and development of Vegetation during the Early Weichselian in Oerel by Behre & Lade (1986).

Occurrence and estimated abundance of planktonic foraminifers at DSDP Leg 85 holes

Tropical planktonic foraminifers occur throughout the sequences at all sites of Leg 85, and the standard planktonic foraminiferal zonation of Blow (1969) is applicable to most of the recovered sequences. However, the abundance and state of preservation of foraminifers decline markedly in certain intervals because of the effects of dissolution. Although siliceous microfossils studied on this leg indicate recovery of nearly complete records for the Pleistocene to Oligocene interval, the planktonic foraminiferal biostratigraphy is interrupted by strongly dissolved sections at all sites. Particularly, faunas assignable to Zone N7 (early Miocene) and Zone N15-16 (early late Miocene) are almost totally unrecognizable throughout the eastern equatorial Pacific. Well-preserved and diverse planktonic foraminifers occur in the lower middle Miocene, where the evolutionary developments of Orbulina universa d'Orbigny and Globorotalia fohsi Cushman and Ellisor are well represented. The Orbulina first appearance datum is observed to be nearly coincident with the last occurrence level of the diatom Annellus californicus Tempère, thus .establishing an age of 15 Ma for this datum by using the paleomagnetic calibration of the diatom datum. Moderately well-preserved late Eocene planktonic foraminifers occur in the carbonate sediments immediately overlying the basalt basement at Sites 573 and 574. The Eocene-Oligocene faunal transition, however, is masked at both sites by an intercalation of metalliferous layers containing no planktonic foraminifers.

Planktonic foraminifers from Oligocene to Pleistocene sediments of DSDP Leg 92 sites

Leg 92 of the Deep Sea Drilling Project cored sediments containing calcareous microfossils at six sites along 19°S latitude in the South Pacific Ocean. Shipboard examination of these sediments revealed planktonic foraminifers of uppermost Oligocene through Pleistocene age that were identified and assigned to biostratigraphic zones according to the tropical zonation scheme of Blow (1969). Preservation of planktonic foraminifers in the sites from Leg 92 has been affected by the position of each site with respect to the lysocline and calcium carbonate compensation depth (CCD) at the time of deposition, depth of burial, and sediment accumulation rate (rate of burial). An additional factor may also be important, especially in the sediments deposited immediately above basement. Evidence of poor preservation in basal sediments of Holes 600C and 601, which have always been shallower than both the lysocline and the CCD, suggests that hydrothermal solutions circulating within young oceanic crust may penetrate the overlying sediments and affect the preservation of calcareous microfossils deposited there.

Biomass of mesozooplankton in the western part of the Black Sea in 1992 during the Cooperative Marine Science Program for the Black Sea (CoMSBlack)

The "CoMSBlack92" dataset is based on samples collected in the summer of 1992 along the Bulgarian coast including coastal and open sea areas. The whole dataset is composed of 79 samples (28 stations) with data of zooplankton species composition, abundance and biomass. Sampling for zooplankton was performed from bottom up to the surface at standard depths depending on water column stratification and the thermocline depth. Zooplankton samples were collected with vertical closing Juday net,diameter - 36cm, mesh size 150 ?m. Tows were performed from surface down to bottom meters depths in discrete layers. Samples were preserved by a 4% formaldehyde sea water buffered solution. Sampling volume was estimated by multiplying the mouth area with the wire length. Sampling volume was estimated by multiplying the mouth area with the wire length. The collected material was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Asen Konsulov using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972 ). The biomass was estimated as wet weight by Petipa, 1959 (based on species specific wet weight). Wet weight values were transformed to dry weight using the equation DW=0.16*WW as suggested by Vinogradov & Shushkina, 1987. Copepods and Cladoceras were identified and enumerated; the other mesozooplankters were identified and enumerated at higher taxonomic level (commonly named as mesozooplankton groups). Large (> 1 mm body length) and not abundant species were calculated in whole sample. The biomass was estimated as wet weight by Petipa, 1959 ussing standard average weight of each species in mg/m**3.

Biomass of mesozooplankton in the western part of the Black Sea in summer 1991 during the NATO Programme Hydroblack

The "Hydroblack91" dataset is based on samples collected in the summer of 1991 and covers part of North-Western in front of Romanian coast and Western Black Sea (Bulgarian coasts) (between 43°30' - 42°10' N latitude and 28°40'- 31°45' E longitude). Mesozooplankton sampling was undertaken at 20 stations. The whole dataset is composed of 72 samples with data of zooplankton species composition, abundance and biomass. Samples were collected in discrete layers 0-10, 0-20, 0-50, 10-25, 25-50, 50-100 and from bottom up to the surface at depths depending on water column stratification and the thermocline depth. Zooplankton samples were collected with vertical closing Juday net,diameter - 36cm, mesh size 150 µm. Tows were performed from surface down to bottom meters depths in discrete layers. Samples were preserved by a 4% formaldehyde sea water buffered solution. Sampling volume was estimated by multiplying the mouth area with the wire length. Mesozooplankton abundance: The collected materia was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Asen Konsulov using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972). The biomass was estimated as wet weight by Petipa, 1959 (based on species specific wet weight). Wet weight values were transformed to dry weight using the equation DW=0.16*WW as suggested by Vinogradov & Shushkina, 1987. Taxon-specific abundance: The collected material was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Copepods and Cladoceras were identified and enumerated; the other mesozooplankters were identified and enumerated at higher taxonomic level (commonly named as mesozooplankton groups). Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Asen Konsulov using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972). The biomass was estimated as wet weight by Petipa, 1959 ussing standard average weight of each species in mg/m3. WW were converted to DW by equation DW=0.16*WW (Vinogradov ME, Sushkina EA, 1987).

Planktonic foraminifera stratigraphy and datum events of ODP Leg 198 sites

During Leg 198 of the Ocean Drilling Program (ODP), Paleogene sediments were recovered form 10 holes at four sites along a bathymetric transect from the Southern High of Shatsky Rise. In terms of age, the Paleogene successions span from the Cretaceous/Paleocene boundary to the early Oligocene. Sediments are mainly composed of tan nannofossil ooze with scattered darker layers richer in clay. This data report concerns planktonic foraminiferal biostratigraphy from three holes, specifically Hole 1209A (water depth = 2387 m), Hole 1210A (water depth = 2573 m), and Hole 1211A (water depth = 2907 m). The thickness of Paleogene sediments is 105.90 m in Hole 1209A, 95.05 m in Hole 1210A, and 56.11 m in the deepest Hole 1211A. Preliminary investigations conducted on board revealed that at Site 1209 the succession was mostly complete, whereas the succession was more condensed at Site 1211.

Middle Eocene-Early Pliocene Subantarctic planktic foraminiferal biostratigraphy of ODP Site 1090 on the Agulhas Ridge, South Atlantic

The analysis of planktic foraminiferal assemblages from Site 1090 (ODP Leg 177), located in the central part of the Subantarctic Zone south of South Africa, provided a geochronology of a 330-m-thick sequence spanning the Middle Eocene to Early Pliocene. A sequence of discrete bioevents enables the calibration of the Antarctic Paleogene (AP) Zonation with lower latitude biozonal schemes for the Middle-Late Eocene interval. In spite of the poor recovery of planktic foraminiferal assemblages, a correlation with the lower latitude standard planktic foraminiferal zonations has been attempted for the whole surveyed interval. Identified bioevents have been tentatively calibrated to the geomagnetic polarity time scale following the biochronology of Berggren et al. (1995). Besides planktic foraminiferal bioevents, the disappearance of the benthic foraminifera Nuttallides truempyi has been used to approximate the Middle/Late Eocene boundary. A hiatus of at least 11.7 Myr occurs between V78 and V71 m composite depth extending from the Early Miocene to the latest Miocene-Early Pliocene. Middle Eocene assemblages exhibit a temperate affinity, while the loss of several planktic foraminiferal species by late Middle to early Late Eocene time reflects cooling. During the Late Eocene-Oligocene intense dissolution caused impoverishment of planktic foraminiferal assemblages possibly following the emplacement of cold, corrosive bottom waters. Two warming peaks are, however, observed: the late Middle Eocene is marked by the invasion of the warmer water Acarinina spinuloinflata and Hantkenina alabamensis at 40.5 Ma, while the middle Late Eocene experienced the immigration of some globigerinathekids including Globigerinatheka luterbacheri and Globigerinatheka cf. semiinvoluta at 34.3 Ma. A more continuous record is observed for the Early Miocene and the Late Miocene-Early Pliocene where planktic foraminiferal assemblages show a distinct affinity with southern mid- to high-latitude faunas.

Neogene planktonic foraminifera from the southern Kerguelen Plateau

With the exception of a brief (2 m.y.) late Miocene-early Pliocene hiatus, an essentially complete Neogene record was recovered on the Kerguelen Plateau in a calcareous biofacies. The stratigraphic distribution of about 30 taxa of Neogene planktonic foraminifers recovered at Sites 747, 748,and 751 (Central and Southern Kerguelen plateaus; approximately 54°-58°S) is recorded. Faunas are characterized by low diversity and high dominance and exhibit a gradual decline in species numbers (reflecting a concomitant increase in biosiliceous forms, particularly diatoms) from about 10 in the early Miocene to 5-8 in the middle Miocene, 3-4 in the late Miocene, to essentially a lone (Neogloboquadrina pachyderma) form in the Pliocene-Pleistocene. A provisional sevenfold biostratigraphic zonation has been formulated that, together with the recovery of a representative Neogene magnetostratigraphic record, may ultimately lead to a correlation with low-latitude magnetobiostratigraphies. The initial appearance of Neogloboquadrina pachyderma is associated with magnetic polarity Chron (MPC) 4 (~7 Ma) and MPC 4A (>8 Ma) at Sites 747 and 751, respectively.