452 resultados para Neurospora crassa
Resumo:
Quantitative study of benthic foraminifers from the upper Miocene to lower Pliocene section at Site 612 (1404 m present water depth) and the Pliocene section at Site 613 (2323 m present water depth) shows no evidence of widespread downslope transport of shallow-water biofacies or reworking of older material in the greater than 150 µm size fraction. In contrast, upper Miocene sediments from Site 604 (2364 m present water depth) show extensive reworking and downslope transport. At Site 612, benthic foraminifers show a succession from an upper Miocene Bolivina alata-Nonionella sp. biofacies, to an uppermost Miocene Bulimina alazanensis biofacies, to a lower Pliocene Cassidulina reflexa biofacies, to an upper Pliocene Melonis barleeanum-Islandiella laevigata biofacies. Evidence suggests that the Pliocene biofacies are in situ, although they could have been transported downslope from the upper-middle bathyal zone. At Site 613, Uvigerina peregrina dominated the "middle" Pliocene, while Globocassidulina subglobosa was dominant in the early and late Pliocene. High abundances of U. peregrina at Site 613 are associated with high values of sedimentary organic carbon.
Resumo:
Benthic foraminiferal assemblages in Mesozoic and Cenozoic sediments were studied at Sites 511, 512, 513, and 514 drilled during Leg 71 in the southwestern Atlantic on the Maurice Ewing Bank and in the Argentine Basin. Benthic foraminifers in almost all stratigraphic subdivisions of Sites 511 and 512 reflect the gradual subsidence of the Falkland Plateau from shelf depths in the Barremian-Albian, when a semiclosed basin with restricted circulation of water masses and anaerobic conditions existed, to lower bathyal depths in the Late Cretaceous and Cenozoic, with an abrupt acceleration at the boundary of Lower and Upper Cretaceous. The composition, distribution, and preservation of Late Cretaceous assemblages of benthic foraminifers suggest considerable fluctuations of the foraminiferal lysocline and the CCD. This is evidenced by dissolution facies and foraminiferal assemblages in which agglutinated and resistant calcareous forms predominated during high stands of the CCD and by calcareous facies in which rich assemblages of calcareous species predominated during low stands. The highest position of the CCD on the Plateau (less than 1500-2000 m) was in the late Cenomanian, Turonian, and Coniacian. In the Santonian and Campanian the CCD was at depths below 1500-2000 meters. At the end of the Campanian the CCD shifted again to depths comparable with those of Cenomanian and Turonian time. In the latest Campanian and the Maestrichtian the CCD was low and nanno-foraminiferal oozes with a rich assemblage of benthic foraminifers accumulated. Foraminiferal assemblages at Sites 513 and 514 in the Argentine Basin also testify to oceanic subsidence from lower bathyal depths in the Oligocene to abyssal ones at present. This process was complicated by the influence of geographical migrations of the Polar Front caused by extensions of the ice sheet in the Antarctic after the opening of the Drake Passage during the Oligocene. In Mesozoic and Cenozoic deposits of the Falkland Plateau and the Argentine Basin seven assemblages of benthic foraminifers were distinguished by age: early-middle Albian, middle-late Albian, Late Cretaceous (including four groups), middle Eocene, late Eocene-early Miocene, middle-late Miocene, and Pliocene-Quaternary. The Albian assemblages contain many species common to the foraminiferal fauna of the Austral Biogeographical Province. The Late Cretaceous assemblage contains, along with Austral species, species common to foraminifers of North America, Western Europe, the Russian platform, and the south of the U.S.S.R. Deep-sea cosmopolitan species prevail in Cenozoic assemblages.
Resumo:
The benthic foraminiferal populations along three traverses across the Northwest African continental margin were analyzed on the base of ca. 60 surface sediment samples. Depth ranges of 213 species were established and the main trends of vertical distribution are compared with those known from adjacent regions. Main faunal breaks occure at 100/200 m and 1000/1500 m depth of water. Some species show latitudinal distribution boundaries and the same applies to population density (standing stock), reflecting the regional distribution of nutrients supply by river discharge and upwelling processes. - High proportions of Bolivina test at the lower slope indicate extended downslope transport.
Resumo:
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.
Resumo:
Late Cenozoic benthic foraminiferal faunas from the Caribbean Deep Sea Drilling Project (DSDP) Site 502 (3052 m) and East Pacific DSDP Site 503 (3572 m) were analyzed to interpret bottom-water masses and paleoceanographic changes occurring as the Isthmus of Panama emerged. Major changes during the past 7 Myr occur at 6.7-6.2, 3.4, 2.0, and 1.1 Ma in the Caribbean and 6.7-6.4, 4.0-3.2, 2.1, 1.4, and 0.7 Ma in the Pacific. Prior to 6.7 Ma, benthic foraminiferal faunas at both sites indicate the presence of Antarctic Bottom Water (AABW). After 6.7 Ma benthic foraminiferal faunas indicate a shift to warmer water masses: North Atlantic Deep Water (NADW) in the Caribbean and Pacific Deep Water (PDW) in the Pacific. Flow of NADW may have continued across the rising sill between the Caribbean and Pacific until 5.6 Ma when the Pacific benthic foraminiferal faunas suggest a decrease in bottom-water temperatures. After 5.6 Ma deep-water to intermediate-water flow across the sill appears to have stopped as the bottom-water masses on either side of the sill diverge. The second change recorded by benthic foraminiferal faunas occurs at 3.4 Ma in the Caribbean and 4.0-3.2 Ma in the Pacific. At this time the Caribbean is flooded with cold AABW, which is either gradually warmed or is replaced by Glacial Bottom Water (GBW) at 2.0 Ma and by NADW at 1.1 Ma. These changes are related to global climatic events and to the depth of the sill between the Caribbean and Atlantic rather than the rising Isthmus of Panama. Benthic foraminiferal faunas at East Pacific Site 503 indicate a gradual change from cold PDW to warmer PDW between 4.0 and 3.2 Ma. The PDW is replaced by the warmer, poorly oxygenated PIW at 2.1 Ma. Although the PDW affects the faunas during colder intervals between 1.4 and 0.7 Ma, the PIW remains the principal bottom-water mass in the Guatemala Basin of the East Pacific.
Resumo:
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
Resumo:
During Leg 188 of the Ocean Drilling Program (ODP), employing JOIDES Resolution, we drilled holes at three sites in the southern Indian Ocean in and near Prydz Bay, East Antarctica, between 28 January and 29 February 2000. The objectives of the voyage were to: - Core through sediments deposited when Antarctica underwent the transition from "greenhouse" to the modern "icehouse" state late in the Eocene or early in the Oligocene, at sites obtaining their sediment from the currently subglacial Gamburtsev Mountains that probably were the site of nucleation of the ice sheet (principally Site 1166); - Obtain a sediment record from times at which major changes in the ice sheet volume and characteristics took place as judged from oxygen isotope records, especially at ~23.7 Ma (Oligocene/Miocene boundary), 12-16 Ma (middle Miocene), and 2.7 Ma (late Pliocene) (mainly Site 1165); and - Sample through the upper Pliocene and Quaternary in an attempt to document fluctuations in the extent of the ice sheet over the continental shelf during the Quaternary (especially Site 1167). Paleogene foraminifer-bearing marine sections were not intersected, and thus discussion of marine sections is restricted to the Neogene. Foraminifers are not major contributors to Leg 188 chronostratigraphy but contribute to paleoenvironmental interpretation, to issues such as carbonate compensation depth (CCD) effects and source and history of sediment, and provide a basis for Sr and d18O studies. Chronostratigraphy for the various sections was compiled from diatoms, radiolarians, and paleomagnetism (Shipboard Scientific Party, 2001, doi:10.2973/odp.proc.ir.188.101.2001). Foraminifers were sporadic rather than continuous except in short intervals; however, the Neogene foraminifers from the region are very poorly known and the new records proved to be of significant value in paleoenvironmental interpretation. Only at Site 1167 did drilling intersect a section that yielded foraminifers virtually throughout. Other than for the very young section at each site, there is virtually no continuity of assemblages between sites and thus each section is treated here as separate and unrelated.
Resumo:
Benthic foraminiferal data from Ocean Drilling Program Site 1098 indicate significant changes in deep-water conditions of the Palmer Deep, western Antarctic Peninsula margin, throughout the Holocene (13 ka to present). The earliest Holocene represents a period of transition from the Last Glacial Maximum (LGM). Cold bottom waters, similar to saline shelf water (SSW), dominated the middle Holocene. The late Holocene in the Palmer Deep has been characterized by alternating dominance of circumpolar deep water (CDW) and saline shelf water. These changes have global oceanographic and climatic implications. We suggest that the middle Holocene bottom-water record, in the absence of circumpolar deep water on the western Antarctic Peninsula shelf, indicates high saline shelf water production and/or weakened circumpolar deep water production during the middle Holocene climatic optimum. The late Holocene benthic foraminiferal record indicates rapidly fluctuating sea-ice conditions and may indicate a teleconnection between the South Pacific and Southern Ocean, thus having implications related to the Southern Oscillation Index.
Resumo:
This study presents a new Miocene biostratigraphic synthesis for the high-latitude northeastern North Atlantic region. Via correlations to the bio-magnetostratigraphy and oxygen isotope records of Ocean Drilling Program and Deep Sea Drilling Project Sites, the ages of shallower North Sea deposits have been better constrained. The result has been an improved precision and documentation of the age designations of the existing North Sea foraminiferal zonal boundaries of King (1989) and Gradstein and Bäckström (1996). All calibrations have been updated to the Astronomically Tuned Neogene Time Scale (ATNTS) of Lourens et al. (2004). This improved Miocene biozonation has been achieved through: the updating of age calibrations for key microfossil bioevents, identification of new events, and integration of new biostratigraphic data from a foraminiferal analysis of commercial wells in the North Sea and Norwegian Sea. The new zonation has been successfully applied to two commercial wells and an onshore research borehole. At these high latitudes, where standard zonal markers are often absent, integration of microfossil groups significantly improves temporal resolution. The new zonation comprises 11 Nordic Miocene (NM) Zones with an average duration of 1 to 2 million years. This multi-group combination of a total of 92 bioevents (70 foraminifers and bolboformids; 16 dinoflagellate cysts and acritarchs; 6 marine diatoms) facilitates zonal identification throughout the Nordic Atlantic region. With the highest proportion of events being of calcareous walled microfossils, this zonation is primarily suited to micropaleontologists. A correlation of this Miocene biostratigraphy with a re-calibrated oxygen isotope record for DSDP Site 608 suggests a strong correlation between Miocene planktonic microfossil turnover rates and the inferred paleoclimatic trends. Benthic foraminifera zonal boundaries appear to often coincide with Miocene global sequence boundaries. The biostratigraphic record is punctuated by four main stratigraphic hiati which show variation in their geographic and temporal extent. These are related to the following regional unconformities: basal Neogene, Lower/Middle Miocene ("mid-Miocene unconformity"), basal Upper Miocene and basal Messinian unconformities. Further coring of Neogene sections in the North Sea and Norwegian Sea may better constrain their extent and their effect on the biostratigraphic record.
Resumo:
Analysis of 66 samples from DSDP Site 263 (Cores 263-4R-4 to 263-29R-4) reveals a unique faunal composition with a predominance of agglutinated taxa, many of them previously unrecorded from any other DSDP and ODP Indian Ocean sites. A total of 66 agglutinated and 31 calcareous taxa are documented and five new species are described: Hippocrepina gracilis n.sp., "Textuluriopsis" elegans n.sp., Aaptotoichus challengeri n.sp., "Gaudryinopsis" pseudobettenstaedti n.sp. and "Gaudryina" cuvierensis n.sp. Three assemblages are recognized based on changes in the composition of dominant taxa and occurrences of stratigraphically important species: (1) a high-diversity Valanginian to Barremian Bulbobaculites-Recurvoides Assemblage (Cores 263-29R to - 18R), comprised of numerous elongate agglutinated forms, rare nodosariids, and variable numbers of tubes and ammodiscids; (2) a moderately diverse Aptian to Albian Rhizammina-Ammodiscus-Glomospira Assemblage (Cores 263-18R to -7R) with highly fluctuating numbers of the nominate taxa and Haplophragmoides, Trochammina, Verneuilinoides spp., and Verneuilina howchini; (3) a very low diversity Albian or younger Assemblage (Cores 263-6R to -4R) containing sparse agglutinated foraminifera, rare nodosariids and rotaliids. We interpret the assemblages as shelf to lower slope and consider them to reflect a deepening palaeobathymetry as the Cuvier margin subsided after the initial breakup of East Gondwana during the Valanginian. Our interpretation is in sharp contrast with initial palaeodepth estimates of less than 100 m, as well as with original chronostratigraphic interpretations based on foraminifera and nannofossils which correlated the base of the recovered interval with the Aptian. The absence of many cosmoplitan forms, despite high diversity suggests strong faunal differentiation in the Austral realm or endemisn within the Cuvier Basin during the Early Cretaceous.
Resumo:
Geomorphology, geology, stratigraphy, lithology and geochemistry of bottom sediments in the South Ocean are under consideration. Regularities of distribution of iron-manganese nodules, features of occurrence of ore components in the nodules, nodule abundance in bottom sediments have been studied.
Resumo:
The family Munnopsidae was the most abundant and diverse among 22 isopod families collected by the ANDEEP deep-sea expeditions in 2002 and 2005 in the Atlantic sector of the Southern Ocean. A total of 219 species from 31 genera and eight subfamilies were analysed. Only 20% species were known to science, and 11% of these were reported outside the ANDEEP area mainly from other parts of the SO or the South Atlantic deep sea. One hundred and five species (50%) were rare, occurring at only 1 or 2 stations. Seventy-two percent of all munnopsid specimens belong to the most numerous 25 species with a total abundance of more than 75 specimens; 5 of these species (40% of all specimens) belong to the main genera of the world munnopsid fauna, Eurycope, Disconectes, Betamorpha, and Ilyarachna. About half of all munnopsid specimens and 34% of all species belong to the subfamily Eurycopinae, which is followed in occurrence by the Lipomerinae (19%). Munnopsinae is the poorest represented subfamily (1.5%). The composition of the subfamilies for the munnopsid fauna of the ANDEEP area differs from that of northern faunas. Lipomerinae show a lower percentage (7%) in the North Atlantic and are absent in the Arctic and in the North Pacific. This subfamily is considered as young and having a centre of origin and diversification in the Southern Ocean. The analyses of the taxonomic diversity and the distribution of Antarctic munnopsids and the distribution of the world fauna of all genera of the family revealed that species richness and diversity of the genera are highest in the ANDEEP area. The investigated fauna is characterised also by high percentage of endemic species, the highest richness and diversity of the main munnopsid genera and subfamily Lipomerinae. This supports the hypothesis that the Atlantic sector of SO deep sea may be considered as the main contemporary centre of diversification of the Munnopsidae. It might serve as a diversity pump of species of the Munnopsidae to more northern Atlantic areas via the deep water originating in the Weddell Sea.