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Early Oligocene siliceous microfossils were recovered in the upper c. 193 m of the CRP-3 drillcore. Although abundance and preservation are highly variable through this section, approximately 130 siliceous microfossil taxa were identified, including diatoms, silicoflagellates, ebridians, chrysophycean cysts, and endoskeletal dinoflagellates. Well-preserved and abundant assemblages characterize samples in the upper c. 70 m and indicate deposition in a coastal setting with water depths between 50 and 200 m. Abundance fluctuations over narrow intervals in the upper c. 70 mbsf are interpreted to reflect environmental changes that were either conducive or deleterious to growth and preservation of siliceous microfossils. Only poorly-preserved (dissolved, replaced, and/or fragmented) siliceous microfossils are present from c. 70 to 193 mbsf. Diatom biostratigraphy indicates that the CRP-3 section down to c. 193 mbsf is early Oligocene in age. The lack of significant changes in composition of the siliceous microfossil assemblage suggests that no major hiatuses are present in this interval. The first occurrence (FO) of Cavitatus jouseanus at 48.44 mbsf marks the base of the Cavitatus jouseanus Zone. This datum is inferred to be near the base of Subchron C12n at c. 30.9 Ma. The FO of Rhizosolenia antarctica at 68.60 mbsf marks the base of the Rhizosolenia antarctica Zone. The FO of this taxon is correlated in deep-sea sections to Chron C13 (33.1 to 33.6 Ma). However, the lower range of R. antarctica is interpreted as incomplete in the CRP-3 drillcore, as it is truncated at an underlying interval of poor preservation: therefore, an age of c. 33.1 to 30.9 Ma is inferred for interval between c. 70 and 50 mbsf. The absence of Hemiaulus caracteristicus from diatom-bearing interval of CRP-3 further indicates an age younger than c. 33 Ma (Subchron C13n) for strata above c. 193 mbsf. Siliceous microfossil assemblages in CRP-3 are significantly different from the late Eocene assemblages reported CIROS-1 drillcore. The absence of H. caracteristicus, Stephanopyxis splendidus, and Pterotheca danica, and the ebridians Ebriopsis crenulata, Parebriopsis fallax, and Pseudoammodochium dictyoides in CRP-3 indicates that the upper 200 m of the CRP-3 drillcore is equivalent to part of the stratigraphic interval missing within the unconformity at c. 366 mbsf in CIROS-1.

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During Ocean Drilling Program (ODP) Leg 105, a thick sequence of lower Eocene to lower Oligocene sediments was recovered from Hole 647A in the southern Labrador Sea. These sediments contain diverse, well-preserved, high-latitude calcareous nannofossil flora. The nannofossil biostratigraphy of the hole indicates the presence of a minor hiatus between Zones NP 16 and NP 17 in the upper middle Eocene and a barren interval separating Zones NP 13 and NP 15. Species abundance is highest within the lower to middle Eocene and starts to decline near the base of the upper Eocene. No major change in the nannoflora was observed across the Eocene/Oligocene boundary, although a slight decrease in species abundance was recorded. The Paleogene calcareous nannofossils of nearby DSDP Site 112 were reexamined and compared with those of Site 647. Several cores were reassigned to different nannofossil zones. The calcareous nannoflora are dominated by high-latitude indicative species and also exhibit a high diversity, which suggests the influence of more temperate water masses in this region during Eocene and Oligocene time. One new subspecies from the middle Eocene, Sphenolithus furcatolithoides labradorensis, is described.

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Uppermost Oligocene through middle Miocene calcareous nannofossil events that were considered potentially useful from a biostratigraphic point of view have been investigated from Ocean Drilling Program Sites 806 and 807 in the western equatorial Pacific Ocean. Comparisons have been made to the corresponding events from other equatorial regions and the mid-latitude North Atlantic. In terms of biostratigraphic reliability, defined by the ability of the pertinent species to provide distinctive marker events and synchroneity over geographic distance, the investigated events can be classified into four general categories: The good markers: last occurrence (LO) Sphenolithus ciperoensis, first occurrence (FO) S. delphix, LO S. delphix, FO S. belemnos, LO S. belemnos, FO S. heteromorphus, termination acme (TA) Discoaster deflandrei, and LO Sphenolithus heteromorphus. The poor markers: LO Helicosphaera recta, TA Cyclicargolithus abisectus, LO Triquetrorhabdulus carinatus, and FO Calcidiscus macintyrei. Ecologically controlled markers with regional value: LO Dictyococcites bisectus, LO Helicosphaera ampliaperta, FO Reticulofenestra pseudoumbilica, LO Cyclicargolithus floridanus, and LO Coronocyclus nitescens. The low abundance markers: FO Discoaster druggii, gradational form of Sphenoliths dissimilis/Sphenolithus belemnos, FO Triquetrorhabdulus rugosus, and FO T. rioensis.

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During Ocean Drilling Program Leg 178 we cored nine sites on the continental rise (Sites 1095, 1096, and 1101), continental shelf (Sites 1097, 1100, 1102, and 1103), and in an inner shelf basin, Palmer Deep (Sites 1098 and 1099), along the Pacific margin of the Antarctic Peninsula. Fossil diatoms are a key group that provides age constraint for these shelf site sediments to allow reconstruction of Antarctic Peninsula glacial history. This paper provides the systematic paleontology of diatoms applied in biostratigraphic and paleoceanographic studies and includes a total of 33 plates. Taxonomic confusion in previous reports, including biostratigraphically useful species such as Thalassiosira inura and Thalassiosira complicata, is discussed. These systematics and taxonomic discussions help to provide a reference for Neogene diatoms in the Southern Ocean.

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Selective degradation of organic matter in sediments is important for reconstructing past environments and understanding the carbon cycle. Here, we report on compositional changes between and within lipid classes and kerogen types (represented by palynomorph groups) in relation to the organic matter flux to the sea floor and oxidation state of the sediments since the early Holocene for central Eastern Mediterranean site ABC26. This includes the initially oxic but nowadays anoxic presapropelic interval, the still unoxidised lower part of the organic rich S1 sapropel, its postdepositionally oxidised and nowadays organic-poor upper part as well as the overlying postsapropelic sediments which have always been oxic. A general ~ 2.3 times increase in terrestrial and marine input during sapropel formation is estimated on the basis of the total organic carbon (TOC), pollen, spore, dinoflagellate cyst, n-alkane, n-alkanol and n-alkanoic acid concentration changes in the unoxidised part of the sapropel. The long-chain alkenones, 1,15 diols and keto-ols, loliolides and sterols indicate that some plankton groups, notably dinoflagellates, may have increased much more. Apart from the terrestrial and surface water contributions to the sedimentary organic matter, anomalous distributions and preservation of some C23-C27 alkanes, alkanols and alkanoic acids have been observed, which are interpreted as a contribution by organisms living in situ. Comparison of the unoxidised S1 sapropel with the overlying oxidised sapropel and the organic matter concentration profiles in the oxidised postsapropelic sediments demonstrates strong and highly selective aerobic degradation of lipids and palynomorphs. There seems to be a fundamental difference in degradation kinetics between lipids and pollen which may be possibly related with the absence of sorptive preservation as a protective mechanism for palynomorph degradation. The n-alkanes, Impagidinium, and Nematosphaeropsis are clearly more resistant than TOC. The n-alkanols and n-carboxylic acids are about equally resistant whereas the pollen, all other dinoflagellate cysts and other lipids appear to degrade considerably faster, which questions the practice of normalising to TOC without taking diagenesis into account. Selective degradation also modifies the relative distributions within lipid classes, whereby the longer-chain alkanes, alcohols and fatty acids disappear faster than their shorter-chain equivalents. Accordingly, interpretation of lipid and palynomorph assemblages in terms of pre- or syndepositional environmental change should be done carefully when proper knowledge of the postdepositional preservation history is absent. Two lipid-based preservation proxies are tested the diol-keto-ol oxidation index based on the 1,15C30 diol and keto-ols (DOXI) and the alcohol preservation index (API) whereby the former seems to be the most promising.

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I recovered well-preserved radiolarian assemblages from the Quaternary sediments drilled at all four sites at the mouth of the Gulf of California during Leg 65. The sites, with positions and water depths averaged for all hole locations per site, are Site 482 - 22°47.4'N, 107°59.6'W; water depth, 3022 meters. Site 483 - 22°53.0'N, 108°44.8' W; water depth, 3070 meters. Site 484 - 23°11.2'N, 108°23.6'W; water depth, 2887 meters. Site 485 - 22°44.9'N, 107°54.2'W; water depth, 2981 meters. The nearly 200 taxa I identified are listed alphabetically in the systematic reference list. The only reliable radiolarian biostratigraphic datum determined for the Quaternary sedimentary section is the highest occurrence of Axoprunum angelinum (Hays) at Sites 483, 484, and 485.

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Eocene-Oligocene radiolarians from Ocean Drilling Program Sites 699, 702, and 703, Leg 114 of the Subantarctic Atlantic were examined in order to extend the tripartite zonation for the recovered cores based on results of similar analysis of Leg 120 submarine sediments from the Indian Ocean. Correlation of the two oceans is made by examining 23 biohorizons and the three zones, Eucyrtidium spinosum, Axoprunum irregularis, and Lychnocanoma conica, in ascending stratigraphic order. One new species, Eucyrtidium nishimurae, is described.

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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.

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Radiolarians are very rare in all Leg 90 sites. They are relatively more frequent only in Neogene sediments from Sites 586 and 594, and in Eocene sediments at Site 592. In this chapter radiolarian abundances are recorded as comparative percentages for 92 Neogene morphotypes at Site 586B. Relative abundances only are estimated at Sites 592 and 594, where preservation is poor to moderate. A tentative correlation of radiolarian events at Hole 586B and Site 594 shows that only a few species can be found in both tropical and subantarctic areas. New evolutionary lineages are proposed. 1. Middle Miocene eucyrtids like Eucyrtidium teuscheri group evolved into a widespread species (E. teuscheri teuscheri) ranging from middle Miocene to Holocene and a temperate species (E. teuscheri orthoporus) ranging from middle Miocene to early Pleistocene. 2. Phormostichoartus pitomorphus appears to be a temperate descendant of the cosmopolitan P. fistula and disappears in early Pleistocene time. 3. The discovery of Lamprocyrtis daniellae n.sp. calls into question the lineage L. heteroporos -> L. nigriniae. 4. The evolution of Lamprocyclas maritalis from an ancestor group (L. aff. maritalis) is located in the early part of the Pterocanium prismatium Zone.

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We have measured the relative abundances of smectite, illite, chlorite, and kaolinite in a composite section of the distal Bengal Fan. Two sources of sediment appear to dominate, a smectite-poor, illite-rich source associated with rapid denudation of the Himalayas and a smectite-rich, illite-poor source probably on the continental margin of the Indian sub-continent. Changes in source appear to be related to uplift in the Himalayas and Tibetan Plateau both directly and through the climatic and oceanographic consequences of uplift.

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Radiolarians were recovered from three of the five holes investigated during Leg 125. Relative abundances are estimated at Holes 782A and 784A, where preservation is poor to good. Rare, poorly preserved radiolarians are present in Hole 786A. Seven radiolarian zones are recognized in the latest early- middle Miocene to early Pleistocene of Holes 782A and 784A. These zones are approximately correlated to the zones of Sanfilippo and others published in 1985.

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Well preserved middle Miocene to Recent radiolarians were recovered from several sites in the Weddell Sea by ODP (Ocean Drilling Program) Leg 113. Low rates of sedimentation, hiatuses, and poor core recovery in some sites are offset by the nearly complete recovery of a late middle Miocene to late Pliocene section at Site 689 on the Maud Rise. Although a hiatus within the latest Miocene exists, this site still provides an excellent reference section for Antarctic biostratigraphy. A detailed radiolarian stratigraphy for the middle Miocene to late Pliocene of Site 689 is given, together with supplemental stratigraphic data from ODP Leg 113 Sites 690, 693, 695, 696, and 697. A refined Antarctic zonation for the middle Miocene to Recent is presented, based on the previous zonations of Hays (1965), Chen (1975), Weaver (1976b), and Keany (1979). The late Miocene radiolarian Acrosphaera australis n. sp. is described and used to define the A. australis zone, ranging from the first appearance of the nominate species to the last appearance of Cycladophora spongothorax (Chen) Lombari and Lazarus 1988. The species Botryopera deflandrei Petrushevskaya 1975 is transferred to Antarctissa deflandrei (Petrushevskaya) n. comb.

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During Leg 123, abundant and well-preserved Neocomian radiolarians were recovered at Site 765 (Argo Abyssal Plain) and Site 766 (lower Exmouth Plateau). The assemblages are characterized by a scarcity or absence of Tethyan taxa. The Berriasian-early Aptian radiolarian record recovered at Site 765 is unique in its density of well-preserved samples and in its faunal contents. Remarkable contrasts exist between radiolarian assemblages extracted from claystones of Site 765 and reexamined DSDP Site 261, and faunas recovered from radiolarian sand layers of Site 765. Clay faunas are unusual in their low diversity of apparently ecologically tolerant species, whereas sand faunas are dominated by non-Tethyan species that have never been reported before. Comparisons with Sites 766 and 261, as well as sedimentological observations, lead to the conclusion that this faunal contrast results from a difference in provenance, rather than from hydraulic sorting. Biostratigraphic dating proved difficult principally because of the paucity or even absence of (Tethyan) species used in published zonations. In addition, published zonations are contradictory and do not reflect total ranges of species. Radiolarian assemblages recovered from claystones at Sites 765 and 261 in the Argo Basin reflect restricted oceanic conditions for the latest Jurassic to Barremian time period. Neither the sedimentary facies nor the faunal associations bear any resemblance to sediment and radiolarian facies observed in typical Tethyan sequences. I conclude that the Argo Basin was paleoceanographically separated from Tethys during the Late Jurassic and part of the Early Cretaceous by its position at a higher paleolatitude and by enclosing landmasses, i.e., northeastern India and the Shillong Block, which were adjacent to the northwestern Australian margin before the opening. Assemblages recovered from radiolarian sand layers are dominated by non-Tethyan species that are interpreted as circumantarctic. Their sudden appearance in the late Berriasian/early Valanginian pre-dates the oceanization of the Indo-Australian break-up (Ml 1, late Valanginian) by about 5 m.y., but coincides with a sharp increase in margin-derived pelagic turbidites. The Indo-Australian rift zone and its adjacent margins probably were submerged deeply enough to allow an intermittent "spillover" of circumantarctic cold water into the Argo Basin, creating increased bottom current activity. Circumantarctic cold-water radiolarians transported into the Argo Basin upwelled along the margin and died en masse. Concomitant winnowing by bottom currents led to their accumulation in distinct radiolarite layers. High rates of faunal change and the sharp increase of bottom current activity are thought to be synchronous with the two pronounced late Berriasian-early Valanginian lowstands in sea level. Hypothetically, both phenomena might have been caused by a glaciation on the Antarctic-Australian continent, which was for the first time isolated from the rest of Gondwana by oceanic seaways as a result of Jurassic and Early Cretaceous seafloor spreading. The absence of typical Tethyan radiolarian species during the late Valanginian to late Hauterivian period is interpreted as reflecting a time of strong influx of circumantarctic cold water following oceanization (Mil) and rapid spreading between southeast India and western Australia. The reappearance and gradual increase in abundance and diversity of Tethyan forms along with the still dominant circumantarctic species are thought to result from overall more equitable climatic conditions during the Barremian and early Aptian and may have resulted from the establishment of an oceanic connection with the Tethys Ocean during the early Aptian.

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Epiclastic volcanogenic rocks recovered from the Kerguelen Plateau during Ocean Drilling Program Legs 119 and 120 comprise (pre-)Cenomanian(?) claystones (52 m thick, Site 750); a Turonian(?) basaltic pebble conglomerate (1.2 m thick, Site 748; Danian mass flows (45 m thick, Site 747); and volcanogenic debris flows of Quaternary age at Site 736 (clastic apron of Kerguelen Island). Pyroclastic rocks comprise numerous Oligocene to Quaternary marine ash layers. The epiclastic sediments with transitional mid-ocean-ridge basalt (T-MORB) origin indicate weathering (Site 750) and erosion (Site 747) of Early Cretaceous T-MORB from a then-emergent Kerguelen Plateau, connected to Late Cretaceous tectonic events. The basal pebble conglomerate of Site 748 has an oceanic-island basalt (OIB) composition and denotes erosion and reworking of seamount to oceanic-island-type volcanic sources. The vitric- to crystal-rich marine ash layers are a few centimeters thick, have rather uniform grain sizes around 60 ± 40 µm, and are a result of Plinian eruptions. Crystal-poor silicic vitric ashes may also represent co-ignimbrite ashes. The ash layers have bimodal, basaltic, and silicic compositions with a few intermediate shards. The basaltic ashes are evolved high-titanium T-MORB; a few grains in a silicic pumice lapilli layer have a low-titanium basaltic composition. The silicic ashes comprise trachytic and rhyolitic glass shards belonging to a high-K series, except for a few low-K glasses admixed to a basaltic ash layer. Feldspar and clinopyroxene compositions fit the glass chemistry: high-Ti tholeiite-basaltic glasses have Plagioclase of An40-80 and pigeonite to augite clinopyroxene compositions. Silicic ashes have K-rich anorthoclase and minor Plagioclase around An20 and ferriaugitic to hedenbergitic clinopyroxene compositions. The line of magmatic evolution for the glass shards is not compatible with simple two-end member (high-Ti T-MORB and high-K rhyolite) mixing, but favors successive Ca-Mg-Fe pyroxene, Ti magnetite, and apatite fractionation, and K-rich alkali feldspar fractionation in trachytic magmas to yield rhyolitic compositions. Plagioclase fractionation occurs throughout. This qualitative model is in basic accordance with the observed mineral assemblage. However, as the time span for explosive volcanism spans >30 m.y., this basic model cannot comply with fractional crystallization in a single magma reservoir. The ash layers resulted from highly explosive eruptions on Kerguelen and, with less probability, Heard islands since the Oligocene. The explosive history starts with widespread Oligocene basaltic ash layers that indicate sea-level or subaerial volcanism on the Northern Kerguelen Plateau. After a hiatus of 24 m.y.(?), explosive magmatic activity was vigorously renewed in the late Miocene with more silicic eruptions. A peak in explosive activity is inferred for the Pliocene-Pleistocene. The composition and evolution of Kerguelen Plateau ash layers resemble those from other hotspot-induced, oceanic-island realms such as Iceland and Jan Mayen in the North Atlantic, and the Canary Islands archipelago in the Central Atlantic.

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The positions of all cores recovered during Leg 90 in the southwest Pacific are shown within the standard calcareous nannoplankton zonation. The stratigraphic and regional occurrences and preservation of Paleogene calcareous nannoplankton found at Sites 588, 592, and 593 are discussed, and fossil lists are given for selected samples. Data on the Eocene/Oligocene boundary found in Holes 592 and 593 and on the Oligocene/Miocene boundary in Hole 588C are presented. Regional unconformities are noted in Hole 588C, where the upper Eocene to middle Oligocene interval (Zones NP17 to NP23) is missing, and in Hole 592, in which the middle Oligocene to lowest Miocene interval (Zones NP23 to NN1) is not represented.