Planktic foraminiferal flux and faunal composition of sediment trap L1_K276 in the northeastern Atlantic

Planktic foraminiferal (PF) flux and faunal composition from three sediment trap time series of 2002-2004 in the northeastern Atlantic show pronounced year-to-year variations despite similar sea surface temperature (SST). The averaged fauna of the in 2002/2003 is dominated by the species Globigerinita glutinata, whereas in 2003/2004 the averaged fauna is dominated by Globigerinoides ruber. We show that PF species respond primarily to productivity, triggered by the seasonal dynamics of vertical stratification of the upper water column. Multivariate statistical analysis reveals three distinct species groups, linked to bulk particle flux, to chlorophyll concentrations and to summer/fall oligotrophy with high SST and stratification. We speculate that the distinct nutrition strategies of strictly asymbiontic, facultatively symbiontic, and symbiontic species may play a key role in explaining their abundances and temporal succession. Advection of water masses within the Azores Current and species expatriation result in a highly diverse PF assemblage. The Azores Frontal Zone may have influenced the trap site in 2002, indicated by subsurface water cooling, by highest PF flux and high flux of the deep-dwelling species Globorotalia scitula. Similarity analyses with core top samples from the global ocean including 746 sites from the Atlantic suggest that the trap faunas have only poor analogs in the surface sediments. These differences have to be taken into account when estimating past oceanic properties from sediment PF data in the eastern subtropical North Atlantic.

(Table 1) Radiolarians of ODP Hole 129-801B

Middle Jurassic radiolarians have been recovered from the western Pacific for the first time. The oldest faunas are assigned to the middle and upper Tricolocapsa conexa Zone, indicating a Bathonian/Callovian age. The faunas contain more than 30 species and are characterized by an abundance of small nassellarians with a constricted distal end. The faunas compare well with Tethyan faunas, and are especially similar to Japanese faunas.

(Table 1) Benthic foraminifera at DSDP Site 72-516

DSDP Site 516 contains a complete middle Eocene to lower Miocene interval with a well-developed Oligocene sequence that is more than 300 m thick. In this paper, the most important and characteristic benthic foraminiferal species from this interval are described and illustrated, and their quantitative and biostratigraphic distribution is given. Middle Eocene benthic assemblages, derived from pelagic intercalations in a partly turbiditic sequence, are low in diversity. Benthic assemblages of fairly high diversity occur in limestones, chalks, and oozes of the upper Eocene to lower Miocene. The consistently high rate of new species appearances at Site 516 during late Eocene and Oligocene contrasted greatly with the very slow rate of change in abyssal faunas at that time; there were no significant faunal changes at the Eocene/Oligocene boundary. The assemblages are dominated by Cibicidoides (mostly C. ungerianus or C. kullenbergi) and Lenticulina. Buliminids were also important during the Eocene and early Oligocene. Faunal comparison with other Atlantic DSDP sites and drill holes in the Gulf of Mexico suggest an approximately mid-bathyal (500-1500 m) depth of deposition during late Eocene and Oligocene.

Biostratigraphy of selected taxa and radiolarian events in ODP Hole 183-1138A sediments

Well-preserved radiolarian assemblages of late middle Miocene to early Pliocene age are found in Ocean Drilling Program (ODP) Hole 1138A (Cores 183-1138A-12R to 20R), which was rotary drilled into the Central Kerguelen Plateau. The faunas are typical for Antarctic assemblages of this time interval, and the site appears to have been south of the Polar Front during the time period studied. Despite only moderate drilling recovery of the section, most late middle to early Pliocene radiolarian zones are present, although at the sample resolution used, subzones could not be identified. A significant discontinuity in the section is present at the boundary between lithologic Units I and II (between Cores 183-1138A-12R and 13R), corresponding to an interval from at least 4.6 to 6.1 Ma. Mixed late Miocene-early Pliocene assemblages are seen in the base of Core 183-1138A-12R (Sample 183-1138A-12R-3, 20 cm), and the overlying basal Pliocene Tau Zone appears to be absent. It cannot be determined if the discontinuity is due to incomplete recovery of the section and drilling disturbance or if it reflects a primary sedimentary structure - a hiatus or interval of condensed sedimentation.

Paleogene and early Neogene planktonic foraminifera of ODP sites 119-738 and 119-744

A virtually complete composite history of Cenozoic pelagic sedimentation was recovered from ODP Sites 738 (62°43' S) and 744 (61°35' S), drilled during Leg 119 on the Kerguelen Plateau. An excellent magnetobiochronologic record was obtained from upper Eocene through Holocene sediments at Site 744, and an expanded lower Paleocene through lower Oligocene sequence was cored at Hole 738. Analysis of the stratigraphic distribution of over 125 planktonic foraminifer taxa from these sites reveals changes in species composition that were strongly influenced by the climatic evolution of Antarctic water masses. Early Paleocene planktonic foraminifer assemblages are nearly identical in species composition to coeval assemblages from low and middle latitude sites, showing the same patterns of post-extinction recovery and taxonomic radiation. Biogeographic isolation, revealed by the absence of tropical keeled species, became apparent by late early Paleocene time. Diversity increased near the Paleocene/Eocene boundary when keeled morozovellids immigrated to the Kerguelen Plateau. Greatest diversity (23 species) was achieved by early Eocene time, corresponding to a Cenozoic warming maximum that has been recognized in lower Eocene deep sea and terrestrial sediments worldwide. A gradual decline in diversity from the late early through middle Eocene, primarily due to the disappearance of acarininids, parallels the record of cooling paleotemperatures in Southern Ocean surface waters. Chiloguembelina-dominated assemblages appeared in the late middle Eocene and persisted through the early Oligocene as Antarctic surface waters became thermally isolated. Late Eocene and early Oligocene assemblages exhibit considerably lower diversity than the older Eocene faunas, and were dominated by chiloguembelinids, subbotinids, and catapsydracids during a time of pronounced climatic cooling and development of continental glaciation on East Antarctica. The small foraminifer Globigerinit? juvenilis replaced chiloguembelinids as the dominant taxon during the late Oligocene. Diversity increased slightly toward the end of the late Oligocene with new appearances of several tenuitellid, globoturborotalitid, and globigerinid species. The trend toward diminishing planktonic foraminifer diversity was renewed during the late early Miocene as siliceous productivity increased in the Antarctic surface waters, culminating with the reduction to nearly monospecific assemblages of Neogloboqu?drin? p?chyderm? that occur in Pliocene-Holocene biosiliceous sediments. An Antarctic Paleogene zonal scheme previously devised for ODP Sites 689 and 690 in the Weddell Sea is used to biostratigraphically subdivide the Kerguelen Plateau sequence. The definition of one Antarctic Paleogene biozone is modified in the present study to facilitate correlation within the southern high latitudes. The ages of 13 late Eoceneearly Miocene datum events are calibrated based on a magnetobiochronologic age model developed for Site 744.

Oligocene plaktonic foraminifera of the Indian Ocean ODP Leg 115 sites

We drilled 13 holes on Ocean Drilling Program Leg 115 in the Indian Ocean and recovered Paleogene sediments that consisted primarily of pelagic components. Planktonic foraminifer assemblages displayed high diversity throughout the Paleogene from the late Paleocene to the Oligocene/Miocene boundary and consist of predominantly warm-water species. Faunas of middle Eocene age are remarkably well represented. Biostratigraphic assignment was, however, very difficult because of the turbiditic character of most of the Paleogene sediments. Reworking is a constant feature of the middle Eocene through early Oligocene planktonic faunas, with reworked faunas frequently overwhelming the younger ones. Preservation within turbidites ranges from excellent to very poor to total destruction of planktonic foraminifers. A major dissolution episode is recorded in the interval that spans most of the late Eocene through the early Oligocene, especially at the deeper sites where the source area was probably well below the lysocline. Redeposition decreases markedly by the mid-Oligocene, but it is only by late Oligocene Zone P22 that normal sedimentation resumes and/or redeposition decreases even at the most affected sites (such as Hole 709C). Comparison with other sites drilled previously in the Indian Ocean reveals that mixed assemblages were already known for sediments from the Mascarene Plateau-Seychelles Bank and surrounding basins during that time span. Because of the disturbances that characterize Paleogene deposits, hiatuses are difficult to detect; nevertheless, a hiatus of less local importance, spanning Subzone P21b, was detected in three holes at different water depths.

Distribution of planktonic foraminifera during the Mid-Pleistocene of ODP Site 181-1123

Planktonic foraminiferal assemblages and artificial neural network estimates of sea-surface temperature (SST) at ODP Site 1123 (41°47.2'S, 171°29.9'W; 3290 m deep), east of New Zealand, reveal a high-resolution history of glacial-interglacial (G-I) variability at the Subtropical Front (STF) for the last 1.2 million years, including the Mid-Pleistocene climate transition (MPT). Most G-I cycles of ~100 kyr duration have short periods of cold glacial and warm deglacial climate centred on glacial terminations, followed by long temperate interglacial periods. During glacial-deglacial transitions, maximum abundances of subantarctic and subtropical taxa coincide with SST minima and maxima, and lead ice volume by up to 8 kyrs. Such relationships reflect the competing influence of subantarctic and subtropical surface inflows during glacial and deglacial periods, respectively, suggesting alternate polar and tropical forcing of southern mid-latitude ocean climate. The lead of SSTs and subtropical inflow over ice volume points to tropical forcing of southern mid-latitude ocean-climate during deglacial warming. This contrasts with the established hypothesis that southern hemisphere ocean climate is driven by the influence of continental glaciations. Based on wholesale changes in subantarctic and subtropical faunas, the last 1.2 million years are subdivided into 4-distinct periods of ocean climate. 1) The pre-MPT (1185-870 ka) has high amplitude 41-kyr fluctuations in SST, superimposed on a general cooling trend and heightened productivity, reflecting long-term strengthening of subantarctic inflow under an invigorated Antarctic Circumpolar Current. 2) The early MPT (870-620 ka) is marked by abrupt warming during MIS 21, followed by a period of unstable periodicities within the 40-100 kyr orbital bands, decreasing SST amplitudes, and long intervals of temperate interglacial climate punctuated by short glacial and deglacial phases, reflecting lower meridional temperature gradients. 3) The late MPT (620-435 ka) encompasses an abrupt decrease in the subantarctic inflow during MIS 15, followed by a period of warm equable climate. Poorly defined, low amplitude G-I variations in SSTs during this interval are consistent with a relatively stable STF and evenly balanced subantarctic and subtropical inflows, possibly in response to smaller, less dynamic polar icesheets. 4) The post-MPT (435-0 ka) is marked by a major climatic deterioration during MIS 12, and a return to higher amplitude 100 kyr-frequency SST variations, superimposed on a long term trend towards cooler SSTs and increased mixed-layer productivity as the subantarctic inflow strengthened and polar icesheets expanded.

Distribution of radiolarians from ODP Leg 128 holes

The analysis of radiolarians from Japan Sea subsurface sediments recovered during Leg 128 of the Ocean Drilling Program reveals that a warm-water assemblage similar to that of the North Pacific was replaced by unique post-middle Miocene faunas probably as a result of the restriction of Oceanographic circulation. The modern fauna was gradually established only in the Pleistocene. No attempt was made to establish the radiolarian zonation because of low species diversity and the absence of generally recognized index forms in the North Pacific. In the diagenetically altered quartz section, however, a radiolarian assemblage correlative to the middle Miocene Cyrtocapsella tetrapera Zone of western Honshu was identified from Hole 799B.

Biostratigraphic and paleomagnetic datum levels in sediments from DSDP Site 85-575

Data on the composition of benthic foraminiferal faunas at Deep Sea Drilling Project Site 575 in the eastern equatorial Pacific Ocean were combined with benthic and planktonic carbon- and oxygen-isotope records and CaCO3 data. Changes in the composition of the benthic foraminiferal faunas at Site 575 predated the middle Miocene period of growth of the Antarctic ice cap and cooling of the deep ocean waters by about 2 m.y., and thus were not caused by this cooling (as has been proposed). The benthic faunal changes may have been caused by increased variability in corrosivity of the bottom waters, possibly resulting from enhanced productivity in the surface waters.

Eocene to Quaternary benthic foraminifers from the Izu-Bonin Arc

The benthic foraminifer fauna at Sumisu Rift Sites 790 and 791 indicates that a deep open-ocean (>2300 m) or a basin with open-ocean access existed between 1.1 and 0.7 Ma at the time of the initiation of rifting. The appearance of a low- to medium-oxygen fauna (1600-2300 m) between 0.7 and 0.5 Ma suggests that the open-ocean access may have been terminated at this time because of the development of volcanoes and rift flank uplifts around the basin. The occurrence of low-oxygen faunas at 0.03 Ma suggests a secondary closing of the basin. The lower bathyal benthic faunas from lower Pliocene sediments of rift margin Site 788 suggest about 0.6-1.6 km of total basement uplift. This uplift may have led to the formation of the major hiatus between 2.3 and <0.3 Ma. The faunal changes of benthic foraminifers at Sites 792 and 793 in the forearc basin document a shallowing water depth from below the carbonate compensation depth (CCD) (about 3.5 km) in the late early Oligocene to the present depths of 1800 and 2975 m, respectively. These data suggest about 1 km of total basement uplift in the inner part of the forearc basin (Site 792) and about 0.6 km total basement subsidence in the central part of the forearc basin (Site 793) since about 31 Ma. The former uplift led to a thinner sediment accumulation (800 m) and the latter subsidence to a thicker sediment accumulation (1400 m) at these sites. Faunal changes of benthic foraminifers observed in Sites 782 and 786 sequences drilled at the outer-arc high document a deepening water depth from 1.3 to 2.1 km in late Eocene to the present depth of about 3 km. These data suggest about 1.1-1.9 and 1.3-2.1 km of total basement subsidence at Sites 786 and 782, respectively. These results indicate total basement uplift in the inner part of the Bonin arc-trench system since late Oligocene and total basement subsidence in the outer part of the system since late Eocene. The last occurrence (LO) of Stilostomella spp. and Pleurostomella spp. and the first occurrence (F0) of Bulimina aculeata d'Orbigny occurred consistently at 0.7 Ma at all three arc proximal sites (790,791, and 792). This fact is taken to suggest a change of water mass, from one originating from the central part of the ocean to that originating from ocean-margin areas at that time.