Foraminiferal species and dissolution index at DSDP Hole 78-541

The calcite compensation depth (CCD) fluctuates as a result of changes in the water-mass system, thereby producing a distinct dissolution pattern. Differential dissolution changes the composition of the foraminiferal assemblages, reflecting the depositional environment in respect to the fluctuating CCD. The dissolution pattern for the comparatively shallow Site 541 on the Barbados Ridge indicates a depositional environment mostly above the CCD, but below the foraminiferal lysocline during the late Miocene to early Pleistocene. In contrast, sediments of the deeper-water Site 543 indicate a depositional environment above the CCD during the late Pliocene to early Pleistocene only. Furthermore, similarities in the dissolution pattern of corresponding time intervals of Site 541 (represented by superimposed faulted intervals termed Tectonic Units A and B) are recognizable. Sediments deposited clearly above the foraminiferal lysocline are rare

Miozene larger foraminifera in ODP Leg 133 holes

The Marion Plateau is a large carbonate platform off northeastern Queensland. Three sites (815, 816, and 826) were drilled on this platform and form the basis for this study. Larger benthic foraminifers, together with rare planktonic forms from the shallow-water carbonates that form the main part of the platform sequence, were studied to establish a biostratigraphy. The presence of Lepidocyclina (Nephrolepidiná) howchini sensu lato and Ladoronia vermicularis, together with Globorotalia (Globorotalia) praemenardii and Orbulina, indicate an early middle Miocene (N9-N12) age (i.e., lower Tf stage) for these carbonates. Dolomitization has destroyed much of the original fabric of these carbonates, making study of the larger foraminifers difficult. Sites 815 (forereef location) and 826 (backreef, lagoonal setting) provide the best faunas. However, at all sites nodular coralline algae and Halimeda are the major bioclasts; coral fragments form a major component at Sites 816 and 826. The middle Miocene neritic sequence is separated from the overlying hemipelagic sequence by an unconformity that spans much of the middle and late Miocene. At Site 815, which is in a forereef situation, the overlying hemipelagic sequence contains a Zone N17A fauna, but at Site 816, higher on the platform, a similar sequence contains a Zone N19 fauna. The faunas indicate that the platform was built up during the early middle Miocene and remained at fairly constant water depths and temperatures during this period. It was then exposed prior to subsiding rapidly during the late Miocene and Pliocene to depths similar to those of the present day.

Planktonic foraminifera abundance in sediments of ODP Leg 170 sites

From October to December in 1996, Sites 1039 through 1043 were drilled on the lower continental slope and the bottom of the Middle American Trench. Planktonic foraminifers were obtained from 377 samples of the total 487 examined. The Pliocene- to Pleistocene-age sediments of Sites 1039 and 1043 are continuous from Zones N19 through N23. At Sites 1039 and 1040, middle Miocene sediments are also continuous, encompassing Zones N8 through N12. The sequences of the upper part of Sites 1040, 1041, 1042, and 1043 are décollements, tentatively assignable to Zone N19 for Sites 1040, 1041, and 1042 and to Zone N22 for Site 1043. The oldest sediments of these sites are assigned to Zone N7 (latest early Miocene), ~17 Ma in age.

Late Miocene to Holocene planktonic foraminifers from ODP Leg 108 holes

Planktonic foraminifers were examined from 27 holes situated at 12 separate sites in the tropical Atlantic. The sites are located in various environments, including areas of upwelling, areas affected by cool currents, areas of strong dissolution, and areas that show little dissolution in warm-water settings. Paleomagnetic results were variable at these sites, but accumulation rate curves have been produced by combining the existing paleomagnetic data with the available microfaunal data. Determinations of the ages of the planktonic foraminifer datums from these accumulation rate curves show some species to be strongly diachronous, while others provide good stratigraphic markers. The warmest water sites with the least dissolution show the most complete ranges of species.

Stable carbon and oxygen isotopes of foraminifera fand carbon content of ODP Leg 107 holes

High-resolution bio- and chemostratigraphy of an earliest Pliocene section from ODP Site 652 indicates that postflood paleoceanographic conditions in the Tyrrhenian Sea can be sub-divided into two discrete intervals. The first is manifested by an acme of Sphaeroidinellopsis spp., increasing carbonate contents, and a progressive decrease upsection in both the d13C and dl8O values of the planktonic foraminifera. The lower part of the acme interval contains unusual surface-to-bottom water isotope gradients suggesting a stratification of two water masses. Normal gradients in the upper part of the acme interval suggest a well-mixed water body. Between the end of the acme interval and the MP11/MP12 boundary, denoted by the first occurrence (F.O.) of Globorotalia margaritae, a migrational first appearance, there was a catastrophic collapse of the gradient marking an onset of the second post-flood interval. The disintegration of habitable conditions is suggested by a sharp decrease in carbonate content and the disappearance of the benthonic assemblage, which is subsequently replaced predominantly by Uvigerinapygmea, indicative of cold, low-oxygenated bottom waters. The introduction of benthonic species denoting well-oxygenated bottom conditions occurs within the lower MP12 zone. Superimposed on these overall trends are shorter term, warm-cold cycles, which are interpreted as orbitally induced, climatic fluctuations. Correlative studies of the less complete earliest Pliocene sections from ODP Holes 653B and 654A confirm these interpretations. A scenario derived from an integration of all the stratigraphic data indicates that normal paleoceanographic conditions were operating in the Tyrrhenian Sea only approximately 250,000 yr after the cessation of Messinian evaporative conditions at the Miocene/Pliocene boundary. The post-flood interval is marked by an initial period of gradual infilling, the Sphaeroidinellopsis spp. acme interval, followed by a disintegration of oceanographic conditions and a second recovery period. A sudden influx of cold, deep Atlantic waters into the Tyrrhenian Sea, resulting from a major tectonic break in the Gibraltar sill, may have caused this catastrophic reversal in the orderly recovery of normal paleoceanographic conditions in the post-flood period.

Planktonic foraminifera of ODP Site 117-722

Quantitative analysis of the late Cenozoic planktonic foraminiferal record from western Arabian Sea Site 722 revealed long term trends in the history of oceanography and climate. The modern western Arabian Sea surface waters are highly influenced by the monsoonal wind system. Summer upwelling, a result of southwestern winds, occurs along the coast of Somalia which produces distinct foraminiferal assemblages which are dominated by G. bulloides d'Orbigny. Consequently, variations in the distribution record of G. bulloides through time monitor the upwelling history associated with monsoonal activities. G. bulloides was a minor constituent of the foraminiferal fauna from the bottom of the hole (~14.5 Ma) until about 8.6 Ma ago. Then a rapid shift occurred toward higher values, up to 53% at 7.4 Ma. We interpret this rapid increase as a major step in the evolution of the monsoonal history. It is either the establishment of the system or at least a strong intensification of the monsoonal winds. At 5.5 Ma a significant drop of the G. bulloides relative abundance occurred which may indicate less upwelling, or alternatively other biota may have been favored in this period. From 5.0 Ma to Recent the G. bulloides record indicates that upwelling has occurred with minor fluctuations.

Calcareous nannofossils and planktonic foraminifera of ODP Hole 132-810C

The 136 m of calcareous oozes recovered in Hole 810C span the interval from upper Maastrichtian to middle Pleistocene. Three major hiatuses interrupt the sequence, with the topmost part of the Maastrichtian through the entire lower Paleocene, most of the lower Eocene, and the entire middle Eocene through most of the middle Miocene missing. Severe reworking and displacement affected the lower part of the succession from the Maastrichtian through the middle Miocene. Reworking and displacement gradually decreased in the upper portion. Calcareous nannofossil biostratigraphy enabled us to calibrate precisely the nearly complete magnetic reversal sequence of the Pliocene to the late Pleistocene. Two minor hiatuses detected by calcareous nannofossils across the Pliocene/Pleistocene boundary and in the upper lower Pleistocene, respectively, resulted in shortening of the Olduvai and Jaramillo Events within the Matuyama Chron of the magnetic reversal sequence.

Planktonic foraminifer stratigraphy of late Pliocene sediments from ODP Hole 167-1021C

This report is an initial investigation of the planktonic foraminifers from the late Pliocene of Ocean Drilling Program Hole 1021C. Planktonic foraminifer assemblages show fair preservation in many samples. Assemblages are quantitatively dominated by Globigerina bulloides, dextral coiling Neogloboquadrina atlantica, and Globorotalia inflata and alternate between cool temperate and subarctic conditions.

Cenozoic plaktonic foraminfers from the Celebes and Sulu Seas

This paper presents the planktonic foraminifer biostratigraphy of the sites drilled during Ocean Drilling Program Leg 124 in the Celebes and Sulu Seas. It discusses preservation of foraminifers in pelagic sediments and in calcareous turbidites. In the Celebes Sea, pelagic carbonates are only found in the Eocene and Oligocene at Site 770. The faunas are poorly preserved due to severe dissolution and offer little biostratigraphic detail. In the Sulu Sea, pelagic carbonates are found in the upper Pliocene and Pleistocene at Sites 768 and 769 and throughout the recovered sequence at the shallower Site 771. The foraminifer faunas from these sediments allow for recognition of most standard zones. Variations in preservation of pelagic foraminifer faunas with time are due to changes in the depth of the lysocline. Shifts to improved preservation at Sites 768 and 769 are synchronous in the upper Pliocene/Pleistocene and may be related to global sea-level cycles. Planktonic foraminifers are also abundant in calcareous turbidites, which were deposited in both basins from the late Miocene onward. However, the turbidites are fine-grained, and biostratigraphic marker species are absent as a result of size-sorting during transport. In the Celebes Sea, shelf-derived material was a major component of early-late Miocene and middle Pliocene to early Pleistocene turbidites. Changes in the composition of the turbidites may correspond to global sea-level changes. In the Sulu Sea, a shift from shelf-derived material in Pliocene calcareous turbidites to a pelagic source in the Pleistocene may be related to subsidence of the Cagayan Ridge.

Pollen record from Blankensee, Germany

Lake Blankensee is filled with 14 m of late- and postglacial deposits, Lake Siethener See with 22,5 m. The lacustrine sedimentation begins in Lake Siethener See in the middle of the Alleröd with annual lamination which partly continues in the Younger Dryas. A 2 cm thick layer of the Laacher See tephra was found in both lakes, the Saksunarvatn tephra only in Lake Siethener See where the cool Rammelbeek-phase (Preboreal) could be shown. The youngest part of the sediment profiles is suspended drifting mud. Masses of Pediastrum (algae) indicate an increasing shoaling of Lake Blankensee after the Subboreal.

Planktonic foraminifera in the trans-tropical Pacific Ocean

Cores from four Ocean Drilling Program (ODP) sites were examined for planktonic foraminifers. One sample per core (from core-catchers in Holes 806B and 807B and from Section 4 in Holes 847B and 852B) was examined through the interval representing the last 5.8 m.y. Sites 806 (0°19.1'N; 159°21.7'E) and 847 (0o12.1'N; 95°19.2'W) are beneath the equatorial divergence zone. Sites 807 (3°36.4'N; 156°37.5'E) and 852 (5°19.6'N; 110°4.6'W) are located north of the equator in the convergence zone created by the interaction of the westward-flowing South Equatorial Current (SEC) and the eastward-flowing North Equatorial Countercurrent (NECC). Specimens were identified to species and then grouped according to depth habitat and trophic level. Species richness and diversity were also calculated. Tropical neogloboquadrinids have been more abundant in the eastern than in the western equatorial Pacific Ocean throughout the last 5.8 m.y. During the mid-Pliocene (3.8-3.2 Ma), their abundance increased at all sites, while during the Pleistocene (after ~ 1.6 Ma), they expanded in the east and declined in the west. This suggests an increase in surface-water productivity across the Pacific Ocean during the closing of the Central American seaway and an exacerbation of the productivity asymmetry between the eastern and western equatorial regions during the Pleistocene. This faunal evidence agrees with eolian grain-size data (Hovan, 1995) and diatom flux data (Iwai, this volume), which suggest increases in tradewind strength in the eastern equatorial Pacific that centered around 3.5 and 0.5 Ma. The present longitudinal zonation of thermocline dwelling species, a response to the piling of warm surface water in the western equatorial region of the Pacific, seems to have developed after 2.4 Ma, not directly after the closing of the Panama seaway (3.2 Ma). Apparently, after 2.4 Ma, the piling warm water in the west overwhelmed the upwelling of nutrients into the photic zone in that region, creating the Oceanographic asymmetry that exists in the modern tropical Pacific and is reflected in the microfossil record. In the upper Miocene and lower Pliocene sediments, the ratio of thermocline-dwelling species to mixed-layer dwellers is 60%:40%. During the mid-Pliocene, the western sites became 40% thermocline and 60% mixed-layer dwellers. Subsequent to -2.4 Ma, the asymmetry increased to 20%: 80% in the west and the reverse in the east. This documents the gradual thickening of the warm-water layer piled up in the western tropical Pacific over the last 5.8 m.y. and reveals two "steps" in the biotic trend that can be associated with specific events in the physical environment.

Late Miocene development of the western Pacific warm pool: Planktonic foraminifer and oxygen isotopic evidence

The disappearance at ~10 Ma of the deep dwelling planktonic foraminifer Globoquadrina dehiscens from the western Pacific including the South China Sea was about 3 Myr earlier than its final extinction elsewhere. Accompanying this event at ~10 Ma was a series of faunal turnover characterized by increase in mixed layer, warm-water species and decrease to a minimum in deepwater species. Paleobiological and isotopic evidence indicates sea surface warming and a deepened local thermocline that we interpret as related to the development of an early western Pacific warm pool. The stepwise decline of G. dehiscens and other deep dwelling species from the NW and SW Pacific suggests more intensive warm water pileup than equatorial localities where surface bypass flow through the narrowing Indonesia seaway appears to remain efficient during the late Miocene. Planktonic delta18O values from the South China Sea consistently lighter than the tropical western Pacific during the Miocene also suggest, similar to today, more variable hydrologic conditions along the periphery than in the core of the warm pool. Stronger hydrologic variability affected mainly by monsoons and increased thermal gradient along the western margin of the late Miocene warm pool may have contributed to the decline of deep dwelling planktonic species including the early extinction of G. dehiscens from the South China Sea region. The late Miocene warm pool became influential and paleobiologically detectable from ~10 Ma, but the modern warm pool did not appear until about 4 Ma, in the middle Pliocene.