Late Quaternary calcareous nannofossils in ODP Leg 139 holes

Upper Quaternary calcareous nannofossils contained in drill cores taken in the heavily sedimented Middle Valley of the northern Juan de Fuca Ridge in the northeast Pacific Ocean (Ocean Drilling Program Leg 139) are investigated. The host sediments have been subjected at depth to high temperatures and hot hydrothermal fluids that have altered or destroyed in part or in toto the nannofossil assemblages, thereby raising at several sites the level of the first (deepest) stratigraphic occurrence of nannofossils or of the important Emiliania huxleyi datum. The degree of alteration of the nannofossil assemblages is dependent on the intensity of the hydrothermal activity, which is indicated by paleotemperatures derived independently from studies of color alteration of palynomorphs and by vitrinite reflectance (Mao et al., this volume). State of preservation and the downhole level at which assemblages have been destroyed correlate well with the inferred paleotemperature estimates. Destruction of the assemblages appears to be species selective and follows in general the dissolution rankings determined independently by others for Recent nannofossils of the Pacific basin. More systematic correlation of these phenomena is hampered, however, by the fact that nannofossil preservation is already quite variable at the time of deposition because of the predominance of turbidite activity in the study area.

Paleocene to middle Eocene calcareous nannofossils of Maude Rise, Weddell Sea

Cores from Sites 689 and 690 of Ocean Drilling Program Leg 113 provide the most continuous Paleocene and Eocene sequence yet recovered by deep sea drilling in the high latitudes of the Southern Ocean. The nannofossil-foraminifer oozes and chalks recovered from Maud Rise at 65°S in the Weddell Sea provide a unique opportunity for biostratigraphic study of extremely high southern latitude carbonate sediments. The presence of warm water index fossils such as the discoasters and species of the Tribrachiatus plexus facilitate the application of commonly used low latitude calcareous nannofossil biostratigraphic zonation schemes for the upper Paleocene and lower Eocene intervals. In the more complete section at Site 690, Okada and Bukry Zones CP1 through CP10 can be identified for the most part with the possible exception of Zone CP3. Several hiatuses are present in the sequence at Site 689 with the most notable being at the Cretaceous/Tertiary and Paleocene/Eocene boundaries. Though not extremely diverse, the assemblage of discoasters in the upper Paleocene and lower Eocene calcareous oozes is indicative of warm, relatively equable climates during that interval. A peak in discoaster diversity in uppermost Paleocene sediments (Zone CP8) corresponds to a negative shift in 5180 values. Associated coccolith assemblages are quite characteristic of high latitudes with abundant Chiasmolithus, Prinsius, and Toweius. Climatic cooling is indicated for middle Eocene sediments by assemblages that contain very abundant Reticulofenestra, lack common discoasters and sphenoliths and are much less diverse overall. Two new taxa are described, Biscutum? neocoronum n. sp. and Amithalithina sigmundii n. gen., n. sp.

Paleocene and Eocene calcareous nannofossils at DSDP Legs 25 and 40 Holes

Paleocene and Eocene nannofossil flora from Deep Sea Drilling Project Legs 25 and 40 were analyzed in order to provide a basis of comparison with DSDP Legs 36 and 71 and with other South Atlantic assemblages. A mid-latitude biostratigraphic zonation, using previously described zonal markers, was adopted for the southwest Indian Ocean. Various diagenetic effects were noted in the sedimentary sequences. Some of these mask to some extent paleoecologic signals, particularly those generated by the Discoaster/Chiasmolithus ratio.

Late Eocene to early Oligocene calcareous nannofossils of ODP Holes 114-699A and 114-703A

Calcareous nannofossil assemblages were studied from Sites 699 and 703, drilled during ODP Leg 114 to the west and east, respectively, of the Mid-Atlantic Ridge in the subantarctic South Atlantic Ocean. Recovery at the two sites consists of an almost continuous sequence of upper Eocene-lower Oligocene sediments. This study describes the calcareous nannofossil assemblages at the transition between the Eocene and Oligocene and correlates these assemblages with those described in lower latitude sections. Quantitative analyses were performed on several important taxa in order to improve the biostratigraphic resolution and permit some paleoenvironmental interpretations. Several discrepancies were noted between the two sites and between the Eocene and Oligocene assemblages. The Eocene assemblages show a great number of species and warmer water conditions; the early Oligocene assemblages are less diversified and are indicative of cooler conditions. The Eocene/Oligocene boundary was not defined by planktonic foraminifers because of the strong dissolution, poor recovery, and drilling disturbances. On the other hand, the calcareous nannofossil assemblage allowed recognition of the interval where the Eocene/Oligocene boundary can possibly be placed.

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.

Distribution of calcareous nannofossils in upper Cretaceous and Cenozoic sediments of the Kerguelen Plateau

ODP Leg 119 drilled 11 sites on the Kerguelen Plateau (southern Indian Ocean) and Prydz Bay (East Antarctica). Upper Pliocene through Quaternary sediments were recovered at Site 736 on the northern Kerguelen Plateau; calcareous nannofossils occurred in only a few samples. Over 700 m of middle Eocene through Quaternary sediments was cored at Site 737 on the northern Kerguelen Plateau, and calcareous nannofossils are abundant in the middle Eocene through the middle Miocene sediments. Nearly 500 m of sediments ranging from the lower Turanian to the Quaternary was recovered at Site 738 on the southern Kerguelen Plateau; calcareous nannofossils are abundant from the Miocene downward. Calcareous nannofossils are also abundant in the upper Eocene through Miocene section from Site 744 on the southern Kerguelen Plateau. Except for Core 119-746A-13H, the Neogene sequences drilled at deep-water Sites 745 and 746 off the southern Kerguelen Plateau are devoid of calcareous nannofossils. Occurrences of calcareous nannofossils were generally rare and sporadic at Sites 739 and 742 in Prydz Bay and suggest that the diamictite sequences recovered is as old as middle Eocene-early Oligocene age. Other sites drilled in Prydz Bay (Sites 740, 741, and 743) did not yield calcareous nannofossils. Species diversity of calcareous nannofossils was low (about a dozen) in the southern Indian Ocean in the Late Cretaceous. High-latitude nanno floral characteristics are apparent after the Cretaceous/Tertiary boundary extinctions. Cold climatic conditions limited Oligocene calcareous nannofossil assemblages to fewer than a dozen species, and extinctions of species generally were not compensated by originations of new species. Only a few species of calcareous nannofossils were found in the Miocene sequences, in which Coccolithuspelagicus and one or two species of Reticulofenestra exhibit extreme (0%-100%) fluctuations in assemblage dominance, and these fluctuations may reflect rapid fluctuations in the surface-water temperatures. Further deterioration of climate in the late Neogene essentially excluded calcareous nannoplankton from the Southern Ocean. Significantly warmer water conditions during part of the early-middle Pleistocene were inferred by a few lower-middle Pleistocene calcareous nannofossil species found on the Kerguelen Plateau. The calcareous nannofossil zonation of Roth (1978 doi:10.2973/dsdp.proc.44.134.1978) can be applied to the Upper Cretaceous section recovered at Site 738, and the zonation of Okada and Bukry (1980 doi:10.1016/0377-8398(80)90016-X) can be applied without much difficulty to the Paleocene to middle Eocene sequences from the Kerguelen Plateau. However, some conventional upper Paleogene markers are not useful for southern high latitudes, whereas a few nonconventional species events are useful for subdividing the upper Paleogene sequences. The latter species events include the first occurrence (FO) of Reticulofenestra reticulata, the FO and last occurrence (LO) of Reticulofenestra oamaruensis, the LO of Isthmolithus recurvus, and the LO of Chiasmolithus altus. As the Neogene sequences from the southern Indian Ocean contain only a few long-ranging, cold-water species, or are devoid of coccoliths, calcareous nannofossil zonations remain virtually unworkable for the Neogene in the high-latitude southern Indian Ocean as in other sectors of the Southern Ocean.

Eocene calcareous nannofossils in DSDP Holes 95-612 and 95-613

Lower Eocene calcareous nannofossil limestone cored at DSDP Site 612 on the middle slope off New Jersey represents an almost complete biostratigraphic sequence; only the lowest biozone (CP9a; NP10*) was not recovered. The thickness of the strata (198 m), the good preservation of the nannofossils, and the lack of long hiatuses justify the acceptance of this section as a lower Eocene reference for the western North Atlantic margin. The widely recognized and very similar nannofossil zonations of Martini (NP zones) and Bukry-Okada (CP zones) are emended slightly to make their lower Eocene biozones coeval; in addition, five new subzones are erected that subdivide zones CP10 and CPU (NP12 and NP13). Established biozone names are retained as they are altered little in concept, but alphanumeric code systems are changed somewhat by appending an asterisk (*) to identify zones that are emended. Zone CP10* (NP12*) is divided into two parts, the Lophodolithus nascens Subzone (CP10*a; NP12*a) and the Helicosphaera seminulum Subzone (CP10*b; NP12*b). Zone CPU* (NP13*) is divided into three parts, the Helicosphaera lophota Subzone (CP11*a; NP13*a), the Cyclicargolithuspseudogammation Subzone (CP11*b; NP13*b), and the Rhabdosphaera tenuis Subzone (CP11*c; NP13*c). At Site 612, a time-depth curve based on nannofossil datums dated in previous studies reveals a smoothly declining sediment accumulation rate, from 4.9 cm/10**3yr in CP10* (NP12*) to 2.8 cm/103 yr. in CP12* (NP14*). The ages of first-occurrence datums not previously dated are approximated by projection onto this timedepth curve and are as follows: Helicosphaera seminulum, 55.0 Ma; Helicosphaera lophota, 54.5 Ma; Cyclicargolithus pseudogammation, 53.7 Ma; Rhabdosphaera tenuis, 52.6 Ma; and Rhabdosphaera inflata, 50.2 Ma. At nearby Site 613 on the upper rise, strata of similar age, 139 m thick, contain an unconformity representing Subzone CPll*b (NP13*b) and a hiatus of approximately 1.1 m.y. duration. The sediment accumulation rate in the lower part of this section (9.7 cm/10**3yr.) is twice that observed for equivalent strata at Site 612. The hiatus and the heightened sediment accumulation rate at Site 613 probably represent the effects of episodic mass wasting on the early Eocene continental slope and rise.

Middle Eocene to Pleistocene calcareous nannofossils of ODP Leg 113 holes

Long sequences of Upper Cretaceous through Quaternary sediments rich in calcareous and siliceous microfossils were recovered at Ocean Drilling Program Sites 689 and 690 on Maud Rise off East Antarctica. These sites have become the southernmost anchor in the Atlantic Basin for bio-, magneto-, chemostratigraphic, and paleobiogeographic studies. ODP Sites 692 and 693 on the Weddell Sea margin of East Antarctica and Site 696 on the South Orkney microcontinent of West Antarctica yielded calcareous nannofossils within some stratigraphic intervals. Sites 691, 692, 694, 695, and 697 did not recover Cenozoic calcareous nannofossils. Calcareous nannofossil biostratigraphy suggests a major hiatus across the Paleogene/Neogene boundary at Sites 689 and 690, and two additional hiatuses in the middle Eocene-lower Oligocene section at Site 690. Correlation with magnetostratigraphy reveals: the last occurrence (LO) of Reticulofenestra umbilica at Maud Rise is over 1 m.y. younger than that at the middle-latitude sites; the LO of Isthmolithus recurvus is synchronous in the middle-latitude and high-latitude areas (about 34.8 Ma); Reticulofenestra oamaruensis ranges from 38.0 to 36.0 Ma at Maud Rise; Reticulofenestra reticulata has a shorter range at Maud Rise (42.1 to 38.9 Ma) than at the middle-latitude DSDP Site 516; the range of Chiasmolithus oamaruensis is diachronous over different latitudes; and the LO of Chiasmolithus solitus is a good datum at 41.3 Ma from 30°S to 65°S in the South Atlantic Ocean. Comparison of calcareous nannofossil abundances in a latitudinal transect shows: Reticulofenestra bisecta is a temperate-water species and its LO, which crosses below that of Chiasmolithus altus at Maud Rise, is not applicable for the Paleogene/Neogene boundary in high southern latitude areas; Clausicoccus fenestratus is rare or absent at Maud Rise and can not be used as a marker; Coccolithus formosus is a warm-water species which disappeared earlier toward higher latitudes. Calcareous nannofossil assemblages indicate that by at least the middle Eocene, surface water temperatures became considerably lower in the high southern latitudes than in the middle-latitude areas and that there have been more extreme cold events in the high latitudes during the Neogene. Bicolumnus ovatus n. gen., n. sp. is proposed in this paper.

Calcareous nannofossils in sediments of the southeast Pacific

This study provides the first detailed documentation of calcareous nannofossil assemblages in Eocene subantarctic Eltanin piston cores recovered from the southeast Pacific Ocean. These Eltanin cores are important because they have been reported to contain ice-rafted quartz. The present study confirms early and middle Eocene ages for the cores and dates them more precisely using calcareous nannofossils. Semiquantitative study of the nannoflora indicates that they are of a warmer water character than those from the higher latitudes (such as Falkland Plateau, Maud Rise, and Kerguelen Plateau). This study concludes that it is unlikely for the ice-rafted quartz in the Eocene sections to be downcore contaminants from the overlying Neogene sediment and suggests that the grains are probably the result of Eocene ice-rafting from Antarctica when the Drake Passage was closed and water circulation patterns were different from those of today.

Calcareous nannofossils from the Sumisu Rift and Izu-Bonin Forearc Basin

During Ocean Drilling Program Leg 126, we recovered three expanded Pleistocene sections from the active backarc rift (Sumisu Rift) and three expanded Oligocene-Miocene sections from the forearc basin of the Izu-Bonin volcanic island arc. Quantitative analysis of the Pleistocene nannofossils revealed five major assemblages between 0 and LO Ma: Assemblage 1 (Holocene-0.085 Ma) contains dominant Emiliania huxleyi; Assemblage 2 (ca. 0.085-0.275 Ma) contains dominant small Gephyrocapsa and common E. huxleyi and Gephyrocapsa oceanica; Assemblage 3 (ca. 0.275-0.6 Ma) contains dominant Gephyrocapsa caribbeanica; Assemblage 4 (ca. 0.6-0.9 Ma) contains a peak abundance of small Gephyrocapsa in the middle part, and dominant occurrences of two types of G. caribbeanica in the lower and upper parts; and Assemblage 5 (ca. 0.9-1.0 Ma) contains dominant small Gephyrocapsa and common G. caribbeanica and Reticulofenestra asanoi. These assemblages are largely synchronous with similar assemblages recognized from tropical and subtropical regions, and can be used for finer subdivision of the Pleistocene than that based on standard Pleistocene nannofossil datums. The Oligocene-Miocene sections contain several hiatuses: up to 3 m.y. may be missing from the uppermost Oligocene (Zone CP19) at Sites 792 and 793; all of Zone CN2 is missing at Sites 792 and 793; part of Zone CN3 and all of Zone CN4 are missing at Site 792. Biochronology of several nannofossil datums at Leg 126 sites indicate that Sphenolithus distentus, Sphenolithus ciperoensis, Cyclicargolithus floridanus, and Discoaster kugleri have diachronous occurrences compared with other sites in the western Pacific Ocean and Philippine Sea.

Calcareous nannofossils from ODP Leg 105 holes

Neogene calcareous nannofossils were examined from 10 holes at three sites cored during ODP Leg 105. Sediment recovered in Baffin Bay at Site 645 is virtually barren of calcareous nannofossils, with the exception of a sparse lower Miocene assemblage. Sites 646 and 647 in the Labrador Sea contain upper Miocene to Holocene sediments having numerous barren intervals. Upper Pleistocene fossil coccolithophorid floras in the Labrador Sea indicate alternations of cold subpolar with transitional (subpolar/subtropical) assemblages. Extreme variations in the abundance of Coccolithus pelagicus were observed at Sites 646 and 647. These variations are correlated with stable isotopic data to interpret oceanographic responses to warming and cooling trends. The climatic history indicated by the changes of these assemblages closely approximates the past climatic fluctuations recorded in other North Atlantic cores. One new taxon, Discoaster bergenii, is described.