946 resultados para Dinoponera australis


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In the course of the ANDEEP-SYSTCO project, during the ANT XXIV-2 expedition in austral summer 2007/2008, the diversity and composition of the Polychaeta of the Antarctic deep-sea and adjacent South Atlantic basins were analyzed. A total of 847 individuals of 31 families were found belonging to 86 different species. Calculation of diversity (Shannon-Wiener Index, Pielou's Evenness) and the general species composition of Polychaeta showed patterns typical for the deep sea, with high species richness and low abundances. Lowest diversity was found in the Agulhas Basin in over 4000 m water depth. Lowest Evenness was found on top of Maud Rise where one-third of all Polychaeta belonged to one species. Cluster analyses resulted in higher affinities of Maud Rise to the Agulhas Basin than to the Antarctic continental slope. Explanations are sought in similarities of environmental factors (e.g., sediment, food input).

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Twenty-three core catcher samples from Site 1166 (Hole 1166A) in Prydz Bay were analyzed for their palynomorph content, with the aims of determining the ages of the sequence penetrated, providing information on the vegetation of the Antarctic continent at this time, and determining the environments under which deposition occurred. Dinocysts, pollen and spores, and foraminiferal test linings were recovered from most samples in the interval from 142.5 to 362.03 meters below seafloor (mbsf). The interval from 142.5 to 258.72 mbsf yielded palynomorphs indicative of a middle-late Eocene age, equivalent to the lower-middle Nothofagidites asperus Zone of the Gippsland Basin of southeastern Australia. The Prydz Bay sequence represents the first well-dated section of this age from East Antarctica. Dinocysts belonging to the widespread "Transantarctic Flora" give a more confident late Eocene age for the interval 142.5-220.5 mbsf. The uppermost two cores within this interval, namely, those from 142.5 and 148.36 mbsf, show significantly higher frequencies of dinocysts than the cores below and suggest that an open marine environment prevailed at the time of deposition. The spore and pollen component may reflect a vegetation akin to the modern rainforest scrubs of Tasmania and New Zealand. Below 267 mbsf, sparse microfloras, mainly of spores and pollen, are equated with the Phyllocladidites mawsonii Zone of southeastern Australia, which is of Turonian to possibly Santonian age. Fluvial to marginal marine environments of deposition are suggested. The parent vegetation from this interval is here described as "Austral Conifer Woodland." The same Late Cretaceous microflora occurs in two of the cores above the postulated unconformity at 267 mbsf. In the core at 249.42 mbsf, the Late Cretaceous spores and pollen are uncontaminated by any Tertiary forms, suggesting that a clast of this older material has been sampled; such a clast may reflect transport by ice during the Eocene. At 258.72 mbsf, Late Cretaceous spores and pollen appear to have been recycled into the Eocene sediments.

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Several studies have shown that submerged macrophytes provide a refuge for zooplankton against fish predation, whereas the role of emergent and floating-leaved species, which are often dominant in eutrophic turbid lakes, is far less investigated. Zooplankton density in open water and amongst emergent and floating-leaved vegetation was monitored in a small, eutrophic lake (Frederiksborg Slotsso) in Denmark during July-October 2006. Emergent and floating-leaved macrophytes harboured significantly higher densities of pelagic as well as plant-associated zooplankton species, compared to the open water, even during periods where the predation pressure was presumably high (during the recruitment of 0+ fish fry). Zooplankton abundance in open water and among vegetation exhibited low values in July and peaked in August. Bosmina and Ceriodaphnia dominated the zooplankton community in the littoral vegetated areas (up to 4,400 ind/l among Phragmites australis and 11,000 ind/l between Polygonum amphibium stands), whereas the dominant species in the pelagic were Daphnia (up to 67 ind/l) and Cyclops (41 ind/l). The zooplankton density pattern observed was probably a consequence of concomitant modifications in the predation pressure, refuge availability and concentration of cyanobacteria in the lake. It is suggested that emergent and floating-leaved macrophytes may play an important role in enhancing water clarity due to increased grazing pressure by zooplankton migrating into the plant stands. As a consequence, especially in turbid lakes, the ecological role of these functional types of vegetation, and not merely that of submerged macrophyte species, should be taken into consideration.

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Twenty-five samples from selected cored intervals of problematic Triassic-Jurassic age from Sites 545, 546, and Hole 547B have been analyzed palynologically to aid age determination. Section 545-73-1 yielded a marine palynoflora of Sinemurian-Bajocian age. A palynoflora of nonmarine origin and assigned a Rhaetian-Hettangian age was recovered from halite in Section 546-18-2. Marine palynofloras of Hettangian-early Pliensbachian age were recovered from Sample 547B-24-CC to Section 547B-14-2. Sections 547B-28-1 to 547B-25-3 yielded impoverished nonmarine palynofloras to which only a general Rhaetian-Hettangian age could be given.

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Radiolarian census and abundance data were collected from three deep-sea cores drilled by the Ocean Drilling Program Sites 884, 887 and 1151 to investigate patterns of ecologic changes in space and time during the last 16 million years for the mid-latitude to subarctic North Pacific. High concentrations of radiolarians occurred between 9.0 and 2.7 Ma. Radiolarian species richness was highest in the early middle Miocene at each site and gradually decreased up to about 7 Ma, coinciding with a well-established global cooling trend. A degree of overlap index calculated for radiolarian assemblages revealed 11 faunal change events, of which 8 corresponded to global cooling events and expansions of polar ice sheets. Three of the faunal change events were observed within the peak of radiolarian accumulation rate and were ascribed to changes in primary productivity in the North Pacific rather than global climatic changes. Our assemblage analyses revealed that north-south differentiation in radiolarian assemblages in the northwestern Pacific has existed since 16 Ma and became more distinct via major steps at 6.8 Ma and 2.7 Ma, coinciding with major glaciation events, and that east-west faunal contrasts in the subarctic region became obvious beginning at 11.7 Ma and changed to a different mode around 6.8 Ma. The observed east-west faunal differences possibly reflect east to west climate differences that were characterized by cooler temperatures in the east than the west during the late Miocene (11.7-6.8 Ma) and then by the opposite temperature trend (6.8 Ma-Recent). A severe glaciation at 2.7 Ma played a large role, particularly in temporal changes in radiolarian accumulation rate and assemblage composition.

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At present time, there is a lack of knowledge on the interannual climate-related variability of zooplankton communities of the tropical Atlantic, central Mediterranean Sea, Caspian Sea, and Aral Sea, due to the absence of appropriate databases. In the mid latitudes, the North Atlantic Oscillation (NAO) is the dominant mode of atmospheric fluctuations over eastern North America, the northern Atlantic Ocean and Europe. Therefore, one of the issues that need to be addressed through data synthesis is the evaluation of interannual patterns in species abundance and species diversity over these regions in regard to the NAO. The database has been used to investigate the ecological role of the NAO in interannual variations of mesozooplankton abundance and biomass along the zonal array of the NAO influence. Basic approach to the proposed research involved: (1) development of co-operation between experts and data holders in Ukraine, Russia, Kazakhstan, Azerbaijan, UK, and USA to rescue and compile the oceanographic data sets and release them on CD-ROM, (2) organization and compilation of a database based on FSU cruises to the above regions, (3) analysis of the basin-scale interannual variability of the zooplankton species abundance, biomass, and species diversity.