790 resultados para Iceland. Alþingi.


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Ostracodes are less common than might be normally expected at Sites 642, 643, and 644, perhaps pointing to the fact that the marine habitat below the overlying Pleistocene ice covers was a severe environment. This explanation, however, would not apply to the Pliocene and Miocene deposits from which ostracodes are just as poorly represented. In the latter case the Iceland-Faeroe Ridge might still have acted as a submerged barrier that did not allow an open ocean circulation of bottom waters. Thus the barrier presumably prevented an exchange of cold subarctic bottom water with that of the open Atlantic and therefore benthic deep-sea migration from the south was impeded. Some Quaternary species are, for the first time, recorded to extend to the Pliocene and/or Miocene.

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Radiolaria are present in frequencies ranging from rare to abundant and with generally moderate to good preservation quality in Leg 104 sediments younger than 22 Ma. Preservation degrades in progressively younger sediments, and upper Pliocene to mid-Pleistocene radiolaria were found only at Site 644, where sporadic assemblages of moderate to poorly preserved specimens persist to approximately 0.75 Ma. Radiolaria are essentially absent in Leg 104 recovery older than basal Miocene. The stratigraphic ranges of 55 taxa of radiolaria are documented in 451 samples from the biosiliceous recoveries of Holes 642B, 642C, 642D, 643A, and 644A. The stratigraphic ranges of 25 of these species are used as boundary criteria for a new system of 28 Neogene zones and subzones that are used to characterize approximately 72% of the past 22 m.y. of sedimentation on the Vriring Plateau. This new scheme is intended to supercede the NRS zones provisionally proposed in the Leg 104 Initial Reports. The applicability of this regional biozonation beyond the Wring and Iceland Plateaus is not presently known. The radiolaria biostratigraphy serves as a basis for inferring a sequence of hiatuses and faunal overturns that may be associated with sea-level low stands and consequent cold-water isolation of the Norwegian Sea. Twenty-one new taxa are described as follows: Actinomma henningsmoeni, Actinomma livae, Actinomma mirabile, Actinomma plasticum, Ceratocyrtis broeggeri, Ceratocyrtis manumi, Ceratocyrtis stoermeri, Clathrospyris vogti, Corythospyris hispida, Corythospyris jubata sverdrupi, Corythospyris reuschi, Crytocapsella ampullacea, Cyrocapsella kladaros, Gondwanaria japonica kiaeri, Hexalonche esmarki, Larcospira bulbosa, Phormospyris thespios, Pseudodicytophimus amundseni, Spongotrochus vitabilis, Spongurus cauleti, and Tessarastrum thiedei.

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The need to obtain ocean color essential climate variables (OC-ECVs) using hyperspectral technology has gained increased interest in recent years. Assessing ocean color on a large scale in high latitude environments using satellite remote sensing is constrained by polar environmental conditions. Nevertheless, on a small scale we can assess ocean color using above-water and in-water remote sensing. Unfortunately, above-water remote sensing can only determine apparent optical properties leaving the sea surface and is susceptible to near surface environmental conditions for example sky and sunglint. Consequently, we have to rely on accurate in-water remote sensing as it can provide both synoptic inherent and apparent optical properties of seawater. We use normalized water leaving radiance LWN or the equivalent remote sensing reflectance RRS from 27 stations to compare the differences in above-water and in-water OC-ECVs. Analysis of above-water and in-water RRS spectra provided very good match-ups (R2 > 0.97, MSE<1.8*10**-7) for all stations. The unbiased percent differences (UPD) between above-water and in-water approaches were determined at common OC-ECVs spectral bands (410, 440, 490, 510 and 555) nm and the classic band ratio (490/555) nm. The spectral average UPD ranged (5 - 110) % and band ratio UPD ranged (0 - 12) %, the latter showing that the 5% uncertainty threshold for ocean color radiometric products is attainable. UPD analysis of these stations West of Greenland, Labrador Sea, Denmark Strait and West of Iceland also suggests that the differences observed are likely a result of environmental and instrumental perturbations.

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The North Atlantic at present is ventilated by overflow of the Denmark Strait, Iceland-Faeroe Ridge, Faeroe Bank Channel, and Wyville-Thompson Ridge. The evolution of Cenozoic abyssal circulation of this region was related to tectonic opening and subsidence of these sills. We used d13C records of the benthic foraminifer Cibicidoides to decipher the timing of tectonically controlled changes in bottom-water circulation in the eastern basins (Biscay and Iberian) of the northern North Atlantic. Records from Site 608 (Kings Trough, northeastern North Atlantic) show that from about 24 to 15 Ma (early to early middle Miocene), d13C values in the Kings Trough area were depleted relative to western North Atlantic values and were more similar to Pacific d13C values. This reflects less ventilation of the Kings Trough region as compared to the well-oxygenated western North Atlantic. Comparison of Oligocene d13C records from Site 119 (Bay of Biscay) with western North Atlantic records suggests that the eastern basin was also relatively isolated prior to 24 Ma. At about 15 Ma, d13C values at Site 608 attained values similar to the western North Atlantic, indicating increased eastern basin ventilation in the middle Miocene. This increased advection into the eastern basin predated a major d18O increase which occurred at about 14.6 Ma. Subsidence estimates of the Greenland-Scotland Ridge indicate that the deepening of the Iceland-Faeroe Ridge was coincident with the marked change in eastern basin deep-water ventilation.