55 resultados para Dinoflagellata


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A well-preserved, diverse sporomorph flora of over 60 species has been found in Cores 120-750B-12W through -14R from the Southern Kerguelen Plateau. Analysis of the flora indicates that the terrestrial sediments overlaying the basaltic basement are late Early Cretaceous in age. Ranges of the sporomorphs in other parts of Gondwana and the morphology and paucity of angiosperm pollen grains confine the age of this section to the early to possibly early middle Albian. The Albian palynomorph assemblages in Hole 750B are composed primarily of fern spores and podocarpaceous pollen, and show most similarity to those from southern Australia. Changes in the flora through time reflect the successional vegetation changes on barren volcanic islands, beginning with high percentages of colonizing ferns and maturing into conifer (podocarp) forests. The flora shows some signs of endemism, which may be a result of the isolated position of the Kerguelen Islands during the Early Cretaceous. This endemism is expressed by high percentages of a distinctive monosulcate pollen species Ashmoripollis woodywisei n.sp. of pteridosperm or cycadophytean origin, and by a thick-walled, monosulcate angiosperm pollen species of the genus Clavatipollenites. The climatic conditions were probably cool to temperate (mean annual temperature approximately 7°-12°C) and humid (annual rainfall >1000 mm), analogous to modern Podocarpus-dominated forests in New Zealand and in South American mountain regions.

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The occurrence of diatom species in the Eocene-Oligocene sections of Ocean Drilling Program (ODP) Leg 115 sites and Deep Sea Drilling Project (DSDP) Sites 219 and 236 in the low-latitude Indian Ocean are investigated. Diatoms are generally rare and poorly preserved in the Paleogene sequences we studied. The best-preserved assemblages are found close to ash layers in early Oligocene sediments. The low-latitude diatom zonation established for the Atlantic region by Fenner in 1984 is fully applicable to the Paleogene sequences of the western Indian Ocean. Correlation of the diatom zones to the calcareous nannofossil stratigraphy of the sites places the Coscinodiscus excavatus Zone of Fenner within calcareous nannofossil Subzone CP16b. For the Mascarene Plateau and the Chagos Ridge, the times when the sites studied, together with the areas upslope from them, subsided to below the euphotic zone are deduced from changes in the relative abundance between the group of benthic, shallow-water species and Grammatophora spp. vs. the group of fully planktonic diatom species. The Eocene section of Site 707, on the Mascarene Plateau, is characterized by the occurrence of benthic diatoms (approximately 10% of the diatom assemblage). These allochthonous diatoms must have originated from shallow-water environments around volcanic islands that existed upslope from ODP Site 707 in Eocene times. In Oligocene and younger sediments of Sites 707 and 706, occurrences of benthic diatoms are rare and sporadic and interpreted as reworked from older sediments. This indicates that the area upslope from these two Mascarene Plateau sites had subsided below the euphotic zone by the early Oligocene. Only Grammatophora spp., for which a neritic but not benthic habitat is assumed, continues to be abundant throughout the Oligocene sequences. The area of the Madingley Rise sites (Sites 709-710) and nearby shallower areas subsided below the euphotic zone already in middle Eocene times, as benthic diatoms are almost absent from these Eocene sections. Only sites located on abyssal plains, and which intermittently received turbidite sediments (e.g., Sites 708 and 711), contain occasionally single, benthic diatoms of Oligocene age. The occurrence of the freshwater diatom Aulacosira granulata in a few samples of late early Oligocene and late Oligocene age at Sites 707, 709, and 714 is interpreted as windblown. Their presence indicates at least seasonally arid conditions for these periods in the source areas of eastern Africa and India. Three new species and two new combinations are defined: Chaetoceros asymmetricus Fenner sp. nov.; Hemiaulus gracilis Fenner, sp. nov.; Kozloviella meniscosa Fenner, sp. nov.; Cestodiscus demergitus (Fenner) Fenner comb, nov.; and Rocella princeps (Jouse) Fenner comb. nov.