Calcareous nannofossil biostratigraphy of ODP Leg 127 sites

Calcareous nannofossils were studied by light microscopy in Neogene sedimentary rocks recovered at four sites of the Ocean Drilling Program Leg 127 in the Japan Sea. Nannofossils occur sporadically at all sites, and allow recognition of seven zones and two subzones; four zones in the Holocene to the uppermost Pliocene, and three zones and two subzones in the middle to lower Miocene. Forty-eight nannofossil species are recognized in 95 of the 808 irregularly-spaced samples taken from all the sites. The nannofossil assemblages in the Miocene are more diverse than those in the Holocene to Pliocene sedimentary interval. The greater diversity and the presence of warm-water taxa, such as Sphenolithus and discoasters in the upper lower Miocene to lower middle Miocene, suggest a relatively warm and stable surface-water condition, attributed to an increased supply of warm water from the subtropical western Pacific Ocean. Site 797 in the southern part of the Yamato Basin contains the most complete and the oldest nannofossil record so far reported from the Japan Sea. The lowermost nannofossil zone at this site, the Helicosphaera ampliaperta Zone (15.7-18.4 Ma) gives a minimum age for the Yamato Basin. This age range predates rotation of southwest Japan, an event previously believed to be caused by the opening of the Japan Sea.

Contribution of woody habitat islands to the conservation of birds and their potential ecosystem services in an extensive Colombian rangeland

The conservation of birds and their habitats is essential to maintain well-functioning ecosystems including human-dominated habitats. In simplified or homogenized landscapes, patches of natural and semi-natural habitat are essential for the survival of plant and animal populations. We compared species composition and diversity of trees and birds between gallery forests, tree islands and hedges in a Colombian savanna landscape to assess how fragmented woody plant communities affect forest bird communities and how differences in habitat characteristics influenced bird species traits and their potential ecosystem function. Bird and tree diversity was higher in forests than in tree islands and hedges. Soil depth influenced woody species distribution, and canopy cover and tree height determined bird species distribution, resulting in plant and bird communities that mainly differed between forest and non-forest habitat. Bird and tree species and traits widely co-varied. Bird species in tree islands and hedges were on average smaller, less specialized to habitat and more tolerant to disturbance than in forest, but dietary differences did not emerge. Despite being less complex and diverse than forests, hedges and tree islands significantly contribute to the conservation of forest biodiversity in the savanna matrix. Forest fragments remain essential for the conservation of forest specialists, but hedges and tree islands facilitate spillover of more tolerant forest birds and their ecological functions such as seed dispersal from forest to the savanna matrix.

Middle Eocene to Miocene calcareous nannofossil of ODP Leg 125

During Ocean Drilling Program Leg 125, a thick sequence of middle Eocene to Pleistocene pelagic sediments, volcanogenic sediments, and predominantly extrusive volcanic rocks was recovered. Calcareous nannofossils were examined from 15 holes at nine sites, but Eocene to Miocene calcareous nannofossils were found only from Holes 782A, 784A, 786A, and 786B. In portions of Holes 786A and 786B, datable nannofossil oozes were found intercalated among volcanic flows. The nannofossil biostratigraphy of these holes indicates the presence of three well-defined hiatuses: within the lower Oligocene, between the upper Oligocene and middle Miocene, and between the middle and upper Miocene. An attempt was made to correlate the magnetochronological data with the first or last occurrences of the following species: Sphenolithus distentus, Reticulofenestra bisecta, Reticulofenestra reticulata, and Cyclicargolithus floridanus abisectus n. comb. The results indicate that the FO of Sphenolithus distentus can extend down to Zone CP16 (34.7 Ma), the LO of Reticulofenestra bisecta best defines the boundary between CP19a and CP19b (23.5 Ma), and the LO of Cyclicargolithus f. abisectus n. comb, can extend up to Subzone CN5a (12.5 Ma). No latest Oligocene Cyclicargolithus f. abisectus n. comb, acme was observed. Cyclicargolithus abisectus is considered a subspecies or variant of Cyclicargolithus floridanus because their LOs coincide. As a consequence of these observations, we have modified the definitions of Bukry's Subzones CP14a, CP14b, and CNla. Analyses of sediment-accumulation rates indicate that the rates increased gradually from the Eocene to Miocene. This is especially evident since the late Miocene in Hole 782A. In different parts of the Izu-Bonin forearc basin, however, the rate is not everywhere the same and appears to vary according to the import of volcanogenic materials.

Sr/Ca ratios of Cenozoic benthic foraminifera

A Cenozoic multi-species record of benthic foraminiferal calcite Sr/Ca has been produced and is corrected for interspecific offsets (typically less than 0.3 mmol/mol) and for the linear relationship between decreasing benthic foraminiferal Sr/Ca and increasing water depth. The water depth correction, determined from Holocene, Late Glacial Maximum and Eocene paleowater-depth transects, is ~0.1 mmol/mol/km. The corrected Cenozoic benthic foraminiferal Sr/Ca record ranges from 1.2 to 2.0 mmol/mol, and has been interpreted in terms of long-term changes in seawater Sr/Ca, enabling issues related to higher-resolution variability in Sr/Ca to be ignored. We estimate that seawater Sr/Ca was ~1.5 times modern values in the late Cretaceous, but declined rapidly into the Paleogene. Following a minimum in the Eocene, seawater Sr/Ca increased gradually through to the present day with a minimum superimposed on this trend centered in the late Miocene. By assuming scenarios for changing seawater calcium concentration, and using published carbonate accumulation rate data combined with suitable values for Sr partition coefficients into carbonates, the seawater Sr/Ca record is used to estimate global average river Sr fluxes. These fluxes are used in conjunction with the seawater strontium isotope curve and estimates of hydrothermal activity/tectonic outgassing to calculate changes in global average river 87Sr/86Sr through the Cenozoic. The absolute magnitude of Sr fluxes and isotopic compositions calculated in this way are subject to relatively large uncertainties. Nevertheless, our results suggest that river Sr flux increased from 35 Ma to the present day (roughly two-fold) accompanied by an overall increase in 87Sr/86Sr (by ~0 to 0.001). Between 75 and 35 Ma, river 87Sr/86Sr also increased (by ~0.001 to 0.002) but was accompanied by a decrease (two- to three-fold) in river Sr flux.

Calcareous nannofossil abundance and datums of sediments from ODP Leg 170 sites

Three Pleistocene, five Pliocene, and thirteen late and middle Miocene calcareous nannofossil datums have been identified in the Leg 170 cored sequences collected from a transect across the Middle America Trench off the Nicoya Peninsula. Although some nannofossil zones could not be delineated, particularly in the Pliocene and upper Miocene, there appears to be a complete or very nearly complete Pleistocene through lower Miocene section at Sites 1039 and 1040. The oldest assemblages, observed at Site 1039 and 1040, are latest early Miocene in age (nannofossil Zone NN4). These assemblages are associated with gabbro intrusions into the basal sediments (one contact metamorphic hornfels sample contains relict nannofossils), indicating an age for the intrusion event of between 15.6 and 18.2 Ma at both Sites 1039 and 1040. Reference Site 1039, located on the Cocos plate, provides the best-preserved sequence of sediments of late Pleistocene to latest early Miocene age. The sediments cored in the prism sections at Sites 1040, 1041, 1042, and 1043 all indicate that the age of nannofossil assemblages in the prism sediments, including the toe, wedge, and apron, are all Pleistocene with a considerable amount of upper Miocene reworking. A period of low sediment accumulation rates (~5.3 m/m.y.) is recorded for Pliocene and upper Miocene sediments at Sites 1039, 1040, and 1043. Pliocene calcareous nannofossil assemblages characteristic of the ~2.5- to 3.75-m.y. time interval (nannofossil Zones NN16 and equivalent nannofossil Subzones CN12b and CN12a) were not resolved at any site. Nannofossil Zones NN15, NN14, NN13, and NN12 (early late Pliocene to early Pliocene) could not be resolved at any site either because of the absence of marker species. Within the Miocene at Sites 1039 and 1040, nannofossil Zones NN10-NN6 were difficult to differentiate because of the absence of several species that define the zonal boundaries. These intervals, where the nannofossil zones have not been resolved or are partially resolved, are primarily composed of carbonate ooze deposited during an ~8.5-m.y. (2.5-11 Ma) low sediment accumulation rate time interval. The absence of many of the marker species is attributed to warmer water conditions during those periods. Many of the same marker species are absent in the sediments recovered from nearby Deep Sea Drilling Project Site 155 in the Panama Basin.

Nannofossil biostratigraphy of ODP Hole 206-1256B sediments

Site 1256 of Ocean Drilling Program Leg 206 to the Guatemala Basin on the eastern flank of the East Pacific Rise yielded a near-complete, middle Miocene-Quaternary carbonate-rich section that provides an opportunity to study low-latitude biostratigraphic and paleoceanographic events. The sedimentary sequence in Hole 1256B has been zoned using calcareous nannofossils according to the biostratigraphic schemes by Martini of 1971 (modified by Martini and Müller in 1986) and Okada and Bukry of 1980. The nannofossil assemblage is characteristic of the low latitudes, with abundant Gephyrocapsa, Discoaster, and Sphenolithus, and is in general moderately to well preserved, depending on nannofossil abundance and the presence of diatoms. Age estimates for the first occurrence and last occurrence of Reticulofenestra rotaria were derived from biostratigraphy and magnetostratigraphy independently and assigned to 7.18 and 6.32 Ma, respectively. Linear sedimentation rates, calculated using 28 nannofossil datums and age estimates, are high in the middle Miocene, decrease from the late Miocene to the Pliocene, then increase upsection. The abrupt drop in carbonate mass accumulation rates during the early late Miocene is referred to as the "carbonate crash." This pattern reflects (1) the long-trend decrease of productivity as the site moves away from the upwelling system at the equatorial divergence as well as (2) fluctuation in the chemistry of the bottom waters associated with production of the North Atlantic Bottom Water and ventilation via the Panama Gateway. A basement age of 14.5 Ma was obtained by extrapolating the 39.1-m/m.y. rate in the middle Miocene to the basement at 250.7 meters below seafloor, and is consistent with the ~15-Ma age of the oceanic crust estimated from marine magnetic anomalies. Reworked nannofossils and lithologic changes were used to unravel postdepositional history, and three episodes were recognized, one of which in the latest Miocene can be widely correlated.

Stable isotope and Mg/Ca ratios of Paleogene benthic foraminifera in the western North Atlantic

Global cooling and the development of continental-scale Antarctic glaciation occurred in the late middle Eocene to early Oligocene (~38 to 28 million years ago), accompanied by deep-ocean reorganization attributed to gradual Antarctic Circumpolar Current (ACC) development. Our benthic foraminiferal stable isotope comparisons show that a large d13C offset developed between mid-depth (~600 meters) and deep (>1000 meters) western North Atlantic waters in the early Oligocene, indicating the development of intermediate-depth d13C and O2 minima closely linked in the modern ocean to northward incursion of Antarctic Intermediate Water. At the same time, the ocean's coldest waters became restricted to south of the ACC, probably forming a bottom-ocean layer, as in the modern ocean. We show that the modern four-layer ocean structure (surface, intermediate, deep, and bottom waters) developed during the early Oligocene as a consequence of the ACC.

(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.

Cenozoic calcareous nannofossils in DSDP Leg 77 holes

Three of the six DSDP Leg 77 sites drilled in the western approaches to the Straits of Florida yielded thick sequences of Cenozoic sediment rich in calcareous nannofossils. Hiatuses are prominent in each of these continuously cored intervals. A prominent upper Oligocene hiatus, observed at each of these three sites, can be correlated to a large-scale "global" regression event. Other disconformable horizons present in the study area cannot be positively related to sealevel fluctuations and may be caused by a number of factors including local tectonic activity. Paleogene sections are generally marked by thick accumulations within the upper Oligocene Sphenolithus ciperoensis Zone and by a pronounced braarudosphaerid-holococcolith bloom recorded in the lower Oligocene and upper Eocene. This bloom is particularly well developed at Site 540. All samples examined contain abundant nannofossils. Preservation fluctuates throughout the sections from good to poor.

Paleogene benthic foraminifera from the Kerguelen Plateau

Benthic foraminifers were studied from lower Paleocene through upper Oligocene sections from Sites 747 and 748. The composition of the benthic foraminifer species suggests a middle to lower bathyal (600-2000 m) paleodepth during the Neogene and a probable upper abyssal (2000-3000 m) paleodepth during the Paleocene at Site 747. Site 748 is thought to have remained at middle to lower bathyal paleodepths throughout the Cenozoic. Principal component analysis distinguished four major benthic foraminifer assemblages: (1) a Paleocene Stensioina beccariiformis assemblage at Sites 747 and 748, (2) an early Eocene Nuttallides truempyi assemblage at lower bathyal Site 747, (3) an early through middle Eocene Stilostomella-Lenticulina assemblage at middle bathyal Site 748, and (4) a latest Eocene through Oligocene Cibicidoides-Astrononion pusillum assemblage at both sites. Major benthic foraminifer changes, as indicated by the principal components and first and last appearances, occurred at or close to the Paleocene/Eocene boundary, and in the late Eocene close to the middle/late Eocene boundary.

Oliogocene to Pleistocene benthic foraminifera in ODP Leg 121 sites

Oligocene to Pleistocene bathyal benthic foraminifers at Broken Ridge (Site 754) and Ninetyeast Ridge (Site 756), eastern Indian Ocean, were investigated for then- stratigraphic distribution and their response to paleoceanographic changes. Q-mode factor analysis was applied to relative abundance data of the most abundant benthic foraminifers. At Site 754, seven varimax assemblages were recognized from the upper Oligocene to the Pleistocene: the Gyroidina orbicularis-Rectuvigerina striata Assemblage in the uppermost Oligocene; the Lenticulina spp. Assemblage in the upper Oligocene to lower Miocene, and in lower Miocene to lowermost middle Miocene; the Burseolina cf. pacifica-Cibicidoides mundulus Assemblage in the lower Miocene; the Planulina wuellerstorfi Assemblage in the upper middle Miocene; the Globocassidulina spp. Assemblage in the upper Miocene; the Gavelinopsis lobatulus-Uvigerina proboscidea Assemblage in the Pliocene; and the Ehrenbergina spp. Assemblage in the Pleistocene. The major faunal changes are complex, but exist between the Lenticulina spp. Assemblage and the P. wuellerstorfi Assemblage at ~13.8 Ma, and between the Ehrenbergina spp. Assemblage and the G. lobatulus Assemblage at ~5 Ma. The development of the P. wuellerstorfi and Globocassidulina spp. Assemblages after 13.8 Ma is correlated with the decrease in temperature of the intermediate waters of the ocean, in turn related to Antarctic glacial expansion. The faunal changes at ~5 Ma are related to the development of low oxygen intermediate water, formed in the presence of a strong thermocline. At Site 756, six varimax assemblages are distributed as follows: the Cibicidoides cf. mundulus-Oridorsalis umbonatus Assemblage in the lower Oligocene; the Epistominella umbonifera-Cibicidoides mundulus Assemblage from the upper Oligocene to the lower Miocene; the Cibicidoides mundulus-Burseolinapacifica Assemblage from lower Miocene to the lower middle Miocene; the Globocassidulina spp. Assemblage from the upper lower Miocene to the Pliocene; the Uvigerina proboscidea Assemblage in the upper Miocene and the Pliocene; and the Globocassidulina sp. D Assemblage in the Pliocene. The main faunal change at this site is between the E. umbonifera Assemblage and the Globocassidulina spp. Assemblage, at ~17.1 Ma. The timing of this faunal change is coeval with faunal changes in the North Atlantic and the Pacific. The change is related to a change in bottom water characteristics caused by an increased influence of carbonate corrosive water from the Antarctic source region, and a change in surface productivity. A low oxygen event at Site 756, which started at about 7.3 Ma, occurred about 2.3 m.y. before that at Site 754. The different response to global paleoceanographic changes is not yet explained, but may be due to the difference of marine topography and the degree of upwelling