Cenozoic calcareous nannofossils from the Lesser Antilles Forearc Region

During Leg 110 of the Ocean Drilling Program, sediment was recovered from six sites in the vicinity of the Lesser Antilles Forearc. Hole 671B, drilled near the toe of the Barbados deformation front, was the first-ever penetration of the decollement between the underthrusting Atlantic Plate and the off scraped Barbados accretionary prism. Stratigraphic repetitions in sequence associated with tectonic movement along the decollement zone, first observed on DSDP Leg 78A, were further documented at four ODP Leg 110 sites. A significant biostratigraphic inversion is present at Site 671 at 128 mbsf in which upper Miocene sediments rest atop lower Pleistocene strata. Smaller repetitions in sequence are recorded at Sites 671, 673, 674, and 676. Leg 110 sediments range from middle Eocene to early Pleistocene in age. Pliocene/Pleistocene assemblages are generally well preserved; however, Miocene assemblages have undergone extensive dissolution at all Leg 110 sites. Paleogene sediments are sometimes recrystallized and the nannofossils contained within exhibit a range in preservation from poor to good.

The Global Plankton Database: an inventory and data from the Former Soviet Union expeditions

At present time, there is a lack of knowledge on the interannual climate-related variability of zooplankton communities of the tropical Atlantic, central Mediterranean Sea, Caspian Sea, and Aral Sea, due to the absence of appropriate databases. In the mid latitudes, the North Atlantic Oscillation (NAO) is the dominant mode of atmospheric fluctuations over eastern North America, the northern Atlantic Ocean and Europe. Therefore, one of the issues that need to be addressed through data synthesis is the evaluation of interannual patterns in species abundance and species diversity over these regions in regard to the NAO. The database has been used to investigate the ecological role of the NAO in interannual variations of mesozooplankton abundance and biomass along the zonal array of the NAO influence. Basic approach to the proposed research involved: (1) development of co-operation between experts and data holders in Ukraine, Russia, Kazakhstan, Azerbaijan, UK, and USA to rescue and compile the oceanographic data sets and release them on CD-ROM, (2) organization and compilation of a database based on FSU cruises to the above regions, (3) analysis of the basin-scale interannual variability of the zooplankton species abundance, biomass, and species diversity.

Cretaceous calcareous nannofossils from Exmouth and Wombat Plateau, Northwest Australia

Three sites drilled during Leg 122, Site 761 on the Wombat Plateau and Sites 762 and 763 on the Exmouth Plateau, provide a composite Cretaceous section ranging in age from Berriasian to Maestrichtian. Together, these sites contain an apparently complete, expanded Aptian-Maestrichtian record. Consistently occurring and moderately well-preserved nannofossil assemblages allow reasonably high biostratigraphic resolution. Our data indicate that traditional middle and Upper Cretaceous nannofossil biozonations are not entirely applicable in this region. In this investigation, we compare in detail the relative ranges of key Cretaceous nannofossil markers in the eastern Indian Ocean and in sections from Europe and North Africa. We have determined which previously used events are applicable, and which additional markers have biostratigraphic utility in this region. Significant differences in Campanian-Maestrichtian assemblages exist between the more northern Site 761 and Sites 762 and 763. Such differences are surprising, considering that these sites are only separated by 3° of latitude. We interpret them as marking a strong thermal gradient over the Exmouth Plateau region. Other results include the recovery of an expanded Albian-Cenomanian sequence containing a mixture of Austral and Tethyan floras, which will enable correlation of biozonations established for these two realms; the recovery of two condensed but apparently complete Cenomanian-Turonian boundary sections; correlation of Upper Cretaceous calcareous nannofossil biostratigraphy with magneto- and foraminifer stratigraphy; and correlation of portions of the Barrow Group equivalents to the Berriasian and Valanginian stages.

Calcareous nannofossil biostratigraphy of ODP Leg 108 sediments

Calcareous nannofossils were examined from the 400 cores recovered at 12 sites during Ocean Drilling Program Leg 108 in the eastern equatorial Atlantic Ocean and along the northwest African margin, representing a transect spanning 24° of latitude. Thirty calcareous nannofossil biohorizons were recognized in the Neogene and Quaternary sequences; only Site 661, located in water depths of 3500 m, contains a fossiliferous record older than the Oligocene. At Site 661, a 200-m-thick sequence of Upper Cretaceous sediments yielded Maestrichtian and uppermost Campanian nannofossils, yet a continuous Cretaceous/Tertiary boundary was not recovered. Widespread sediment slumps and turbidites deposited at many sites interrupted the pelagic sedimentation. A careful study of calcareous nannofossil and foraminifer assemblages correlated to paleomagnetic records suggests that "slumped" units at most sites were added as extra sediments to rapidly deposited pelagic sediments, with minor disturbance of the surrounding layers. Nannofossils are generally common to abundant and moderately preserved at all sites except for those located in two upwelling areas, where placoliths are etched and discoasters overgrown. Typical low-latitudinal zonal markers were used during this study, yet some of them were considered to be of little biostratigraphic value because of their inconsistent stratigraphic ranges and low abundances. This is especially apparent for the intervals representing the Miocene/Pliocene and Oligocene/Miocene boundaries. Characteristic nannofossils of cool-water conditions and low discoaster abundances occur at the coastal African upwelling and along the south equatorial divergence sites, signifying a stronger advection of cold waters toward the equator within the Canary and Benguela eastern boundary currents.

(Table 2) Concentrations of polychlorinated naphthalene congeners in blubber samples from whales, seals and porpoises between 1986-2009

A selection of PCN congeners was analyzed in pooled blubber samples of pilot whale (Globicephala melas), ringed seal (Phoca hispida), minke whale (Balaenoptera acutorostrata), fin whale (Balaenoptera physalus), harbour porpoise (Phocoena phocoena), hooded seal (Cystophora cristata) and Atlantic whitesided dolphin (Lagenorhynchus acutus), covering a time period of more than 20 years (1986-2009). A large geographical area of the North Atlantic and Arctic areas was covered. PCN congeners 48, 52, 53, 66 and 69 were found in the blubber samples between 0.03 and 5.9 ng/g lw. Also PCBs were analyzed in minke whales and fin whales from Iceland and the total PCN content accounted for 0.2% or less of the total non-planar PCB content. No statistically significant trend in contaminant levels could be established for the studied areas. However, in all species except minke whales caught off Norway the lowest Sum PCN concentrations were found in samples from the latest sampling period.

Neogene calcareous nannofossils in ODP Leg 116 holes

The three sites (717, 718, and 719) drilled on the distal Bengal Fan during ODP Leg 116 cored turbidite sediments almost exclusively. Calcareous nannofossils were recovered sporadically and, although all of them probably have been redeposited, it is possible to date the sediments at all three sites with reasonable confidence. Site 717 penetrated the uppermost middle Miocene Catinaster coalitus highest occurrence datum and represents the most nearly continuous succession of turbidites. Site 718 penetrated the lower Miocene, well below the Helicosphaera ampliaperta highest occurrence datum, but this site contains a major late Pliocene to mid-Pleistocene hiatus. Site 719, the shallowest hole, penetrated only into the upper Miocene. Identification of several critical lowest occurrence datums allows using the poorly constrained but more numerous highest occurrence datums for comparison with the model succession (zonal markers) and thereby to derive a reasonably accurate time framework for the sediments.

Benthic foraminifera and stable isotope composition in Paleocene-Eocene sediments

In the late Paleocene to early Eocene, deep sea benthic foraminifera suffered their only global extinction of the last 75 million years and diversity decreased worldwide by 30-50% in a few thousand years. At Maud Rise (Weddell Sea, Antarctica; Sites 689 and 690, palaeodepths 1100 m and 1900 m) and Walvis Ridge (Southeastern Atlantic, Sites 525 and 527, palaeodepths 1600 m and 3400 m) post-extinction faunas were low-diversity and high-dominance, but the dominant species differed by geographical location. At Maud Rise, post-extinction faunas were dominated by small, biserial and triserial species, while the large, thick-walled, long-lived deep sea species Nuttallides truempyi was absent. At Walvis Ridge, by contrast, they were dominated by long-lived species such as N. truempyi, with common to abundant small abyssaminid species. The faunal dominance patterns at the two locations thus suggest different post-extinction seafloor environments: increased flux of organic matter and possibly decreased oxygen levels at Maud Rise, decreased flux at Walvis Ridge. The species-richness remained very low for about 50 000 years, then gradually increased. The extinction was synchronous with a large, negative, short-term excursion of carbon and oxygen isotopes in planktonic and benthic foraminifera and bulk carbonate. The isotope excursions reached peak negative values in a few thousand years and values returned to pre-excursion levels in about 50 000 years. The carbon isotope excursion was about -2 per mil for benthic foraminifera at Walvis Ridge and Maud Rise, and about -4 per mil for planktonic foraminifera at Maud Rise. At the latter sites vertical gradients thus decreased, possibly at least partially as a result of upwelling. The oxygen isotope excursion was about -1.5 per mil for benthic foraminifera at Walvis Ridge and Maud Rise, -1 per mil for planktonic foraminifera at Maud Rise. The rapid oxygen isotope excursion at a time when polar ice-sheets were absent or insignificant can be explained by an increase in temperature by 4-6°C of high latitude surface waters and deep waters world wide. The deep ocean temperature increase could have been caused by warming of surface waters at high latitudes and continued formation of the deep waters at these locations, or by a switch from dominant formation of deep waters at high latitudes to formation at lower latitudes. Benthic foraminiferal post-extinction biogeographical patterns favour the latter explanation. The short-term carbon isotope excursion occurred in deep and surface waters, and in soil concretions and mammal teeth in the continental record. It is associated with increased CaC03-dissolution over a wide depth range in the oceans, suggesting that a rapid transfer of isotopically light carbon from lithosphere or biosphere into the ocean-atmosphere system may have been involved. The rapidity of the initiation of the excursion (a few thousand years) and its short duration (50 000 years) suggest that such a transfer was probably not caused by changes in the ratio of organic carbon to carbonate deposition or erosion. Transfer of carbon from the terrestrial biosphere was probably not the cause, because it would require a much larger biosphere destruction than at the end of the Cretaceous, in conflict with the fossil record. It is difficult to explain the large shift by rapid emission into the atmosphere of volcanogenic CO2, although huge subaerial plateau basalt eruptions occurred at the time in the northern Atlantic. Probably a complex combination of processes and feedback was involved, including volcanogenic emission of CO2, changing circulation patterns, changing productivity in the oceans and possibly on land, and changes in the relative size of the oceanic and atmospheric carbon reservoirs.