951 resultados para Upper bound estimate


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Features of spatial variability of hydrogen sulfide in the northeastern part of the Black Sea are estimated. Some technical aspects of H2S concentration determination in the anoxic zone are discussed: in its upper part at H2S concentration <30 µmol/l, the photometric method is recommended, while for deeper layers the iodometric method should be used. With linearity of vertical distribution of hydrogen sulfide and ammonium taken into account their vertical gradients are estimated as 0.49+/-0.04 µmol/m and 0.19+/-0.06 µmol/m respectively. It is shown that the upper boundary of the H2S layer corresponds to the isopycnal surface with Sigma_t = 16.19+/-0.05 arbitrary units. Special attention is paid to relationship of hydrogen sulfide distribution with hydrophysical features in the region under study, in particular in the coastal zone. It is shown that hydrodynamic conditions control spatial distribution of hydrogen sulfide. On the basis of isopycnal treatment of the H2S field existence of a coastal convergence zone is proved, and peculiarities are recognized of vertical circulation in the main Black Sea gyre and coastal anticyclonic eddies; here hydrogen sulfide serves as a tracer of hydrophysical mixing processes.

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The voluminous volcanic eruptions in the Nauru Basin, Western Pacific, have long been regarded as important research targets for tectonic history of the Pacific Plate and for the widespread Cretaceous volcanic activity in the Western Pacific. The Nauru Basin volcanic rocks were recovered at Site 462 by Deep Sea Drilling Project (DSDP) Legs 61 and 89, where more than 600 m of lavas and sills were drilled, thereby making it the deepest penetration into crust of Cretaceous age in the Pacific Ocean. For paleomagnetism, this section represents a unique possibility for averaging out secular variation to obtain a reliable paleolatitude estimate. However, previous paleomagnetic studies have only been subjected to alternating field (AF) demagnetization on several core samples, thus, unable to provide comprehensive understanding on the paleolatitude of the basin. The work reported here aims to determine the Cretaceous paleomagnetic paleolatitude for the Pacific Plate and define the magnetostratigraphy for the basaltic sections drilled in the Nauru Basin. A total of 391 basaltic rock samples were carefully re-sampled from DSDP Sites 462 and 462A. Stepwise thermal and AF demagnetizations have isolated characteristic components in the majority of the samples. The most important findings from this study include: (1) Two normal and one reversed polarity intervals are identified in Site 462, and six normal and six reversed polarity intervals are found in Site 462A, although possible erroneous markings of the opposite azimuth for some reversed polarity cores during the DSDP coring cannot be completely ruled out. (2) Based on previous radiometric ages, the magnetostratigraphic correlations with the Geomagnetic Polarity Time Scale (GPTS) indicate that the lower-basaltic flow unit in Site 462A began to erupt at least before 130 Ma. No correlation is available for the upper-sill unit. (3) Paleosecular variation for the lower-flow unit has been sufficiently averaged out; whereas bias may exist for that of the upper-sill unit; (4) The calculated mean inclination of ~50° for the lower-flow unit yields a paleolatitude of 30.8°S for the Nauru Basin at the time of emplacement. This value is well to the north of suggested location in plate reconstruction models, suggesting that there has been a significant amount of apparent polar wander of the Nauru Basin and Pacific plate since 130 Ma. In addition, the paleolatitude for the Nauru Basin is ~7° further south and the basin's age is more than 10 my older than those of the Ontong Java Plateau (OJP), which suggest that the volcanic eruptions of the lower flows in the Nauru Basin are unlikely related to the emplacement of the Ontong Java Plateau.

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This paper documents the biostratigraphic distribution and abundance of diatoms from sites drilled during Ocean Drilling Program Leg 178, off the Pacific margin of the Antarctic Peninsula. Drift sediments cored on the continental rise at Sites 1095, 1096, and 1101 have good recovery and a well-defined paleomagnetic record. Well-preserved diatoms are present throughout the upper Miocene to middle Pliocene and in the upper Quaternary section of these sites. The stratigraphic occurrence of diatom species through these intervals defines numerous datum levels. Diatom events are given absolute age estimates through direct correlation to the established paleomagnetic stratigraphy of Sites 1095, 1096, and 1101. Leg 178 diatom biostratigraphic results enable the development of a regional stratigraphic framework for the Pacific sector of the Southern Ocean and record the interaction of open-ocean and shelf-margin diatom floras.

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Nitrogen fixation data from the cruise number MSM18/5 with research vessel "Maria S. Merian" from 22.08.-20.09.2011 (from Walvis Bay to Walvis Bay) in front of Angola and northern Namibia. Samples taken by CTD- rosette sampler from different depths and incubated in glass bottles (535 ml) at light intensities that resemble the in situ light intensities of the sampling depth after 15N2 gas was injected to the sample. After the incubation time of 6 hours, the complete bottle content was filtered onto a pre-combusted Whatman GF/F filter. Filters were frozen, transported to the institute on dry ice and measured in a mass spectrometer for Delta 15N. The principle of the method was described by Montoya et al. (1996) and calculation was done according to their spread sheet. From the data of the single depths, the nitrogen fixation per square meter within the upper 40 m of the water column was calculated. The methods are described in detail in a paper submitted by Wasmund et al. in 2014 to be printed in 2015. Some results are surprisingly below zero. This occurs if the Delta 15N of the blank is higher than the measurement after incubation. It indicates that no nitrogen fixation occurred. Due to natural variability, the variability of the nitrogen fixation data is high. In an overall estimate, also over several cruises, negative and positive values compensate more or less, suggesting that nitrogen fixation is insignificant in the waters in front of northern Namibia and southern Angola.

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ODP Leg 119 drilled 11 sites on the Kerguelen Plateau (southern Indian Ocean) and Prydz Bay (East Antarctica). Upper Pliocene through Quaternary sediments were recovered at Site 736 on the northern Kerguelen Plateau; calcareous nannofossils occurred in only a few samples. Over 700 m of middle Eocene through Quaternary sediments was cored at Site 737 on the northern Kerguelen Plateau, and calcareous nannofossils are abundant in the middle Eocene through the middle Miocene sediments. Nearly 500 m of sediments ranging from the lower Turanian to the Quaternary was recovered at Site 738 on the southern Kerguelen Plateau; calcareous nannofossils are abundant from the Miocene downward. Calcareous nannofossils are also abundant in the upper Eocene through Miocene section from Site 744 on the southern Kerguelen Plateau. Except for Core 119-746A-13H, the Neogene sequences drilled at deep-water Sites 745 and 746 off the southern Kerguelen Plateau are devoid of calcareous nannofossils. Occurrences of calcareous nannofossils were generally rare and sporadic at Sites 739 and 742 in Prydz Bay and suggest that the diamictite sequences recovered is as old as middle Eocene-early Oligocene age. Other sites drilled in Prydz Bay (Sites 740, 741, and 743) did not yield calcareous nannofossils. Species diversity of calcareous nannofossils was low (about a dozen) in the southern Indian Ocean in the Late Cretaceous. High-latitude nanno floral characteristics are apparent after the Cretaceous/Tertiary boundary extinctions. Cold climatic conditions limited Oligocene calcareous nannofossil assemblages to fewer than a dozen species, and extinctions of species generally were not compensated by originations of new species. Only a few species of calcareous nannofossils were found in the Miocene sequences, in which Coccolithuspelagicus and one or two species of Reticulofenestra exhibit extreme (0%-100%) fluctuations in assemblage dominance, and these fluctuations may reflect rapid fluctuations in the surface-water temperatures. Further deterioration of climate in the late Neogene essentially excluded calcareous nannoplankton from the Southern Ocean. Significantly warmer water conditions during part of the early-middle Pleistocene were inferred by a few lower-middle Pleistocene calcareous nannofossil species found on the Kerguelen Plateau. The calcareous nannofossil zonation of Roth (1978 doi:10.2973/dsdp.proc.44.134.1978) can be applied to the Upper Cretaceous section recovered at Site 738, and the zonation of Okada and Bukry (1980 doi:10.1016/0377-8398(80)90016-X) can be applied without much difficulty to the Paleocene to middle Eocene sequences from the Kerguelen Plateau. However, some conventional upper Paleogene markers are not useful for southern high latitudes, whereas a few nonconventional species events are useful for subdividing the upper Paleogene sequences. The latter species events include the first occurrence (FO) of Reticulofenestra reticulata, the FO and last occurrence (LO) of Reticulofenestra oamaruensis, the LO of Isthmolithus recurvus, and the LO of Chiasmolithus altus. As the Neogene sequences from the southern Indian Ocean contain only a few long-ranging, cold-water species, or are devoid of coccoliths, calcareous nannofossil zonations remain virtually unworkable for the Neogene in the high-latitude southern Indian Ocean as in other sectors of the Southern Ocean.

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Eight different sites from 2300 to 4420 m water depth in the Arabian Sea were sampled for a biochemical quantification of phospholipid concentrations in the sediments. This method serves as a measure of microbial biomass in marine sediments comprising all small-sized organisms, including bacteria, fungi, protozoa and metazoa. Phospholipid concentrations can be converted to carbon units as an estimate of total microbial biomass in the sediments. The average phospholipid concentrations in the surface sediments (0-1 cm) of the 4 abyssal sites ranged from 7 nmol cm?3 at the southern site (SAST, 10°N 65°E, 4425 m) to 29 nmol/cm**3 at the western site (WAST, 16°N 60°E, 4045 m). The high values detected at the abyssal station WAST exceeded those in the literature for other abyssal sites and were comparable to values from the upper continental slope of the NE-Atlantic and the Arctic. At the four continental slope sites in the Arabian Sea, average phospholipid concentrations ranged from 9 to 53 nmol/cm**3 with the maximum values at stations A (2314 m) and D (3142 m) close to the Omani coast. Records of particulate organic carbon flux to the deep sea are available for four of the investigated locations, allowing a test of the hypothesis that the standing stock of benthic microorganisms in the deep sea is controlled by substrate availability, i.e. particle sedimentation. Total microbial biomass in the surface sediments of the Arabian Sea was positively correlated with sedimentation rates, consistent with previous studies of other oceans. The use of the measurement of phospholipid concentrations as a proxy for input of particulate organic matter is discussed.

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Recent evidence that dissolved organic carbon (DOC) is a significant component of the organic carbon flux below the photic layer of the ocean (1), together with verification of high respiration rates in the dark ocean (2), suggests that the downward flux of DOC may play a major role in supporting respiration there. Here we show, on the basis of examination of the relation between DOC and apparent oxygen utilization (AOU), that the DOC flux supports ~10% of the respiration in the dark ocean. The contribution of DOC to pelagic respiration below the surface mixed layer can be inferred from the relation between DOC and apparent oxygen utilization (AOU, µM O2), a variable quantifying the cumulative oxygen consumption since a water parcel was last in contact with the atmosphere. However, assessments of DOC/AOU relations have been limited to specific regions of the ocean (3, 4) and have not considered the global ocean. We assembled a large data set (N = 9824) of concurrent DOC and AOU observations collected in cruises conducted throughout the world's oceans (fig. S1, table S1) to examine the relative contribution of DOC to AOU and, therefore, respiration in the dark ocean. AOU increased from an average (±SE) 96.3 ± 2.0 µM at the base of the surface mixed layer (100 m) to 165.5 ± 4.3 µM at the bottom of the main thermocline (1000 m), with a parallel decline in the average DOC from 53.5 ± 0.2 to 43.4 ± 0.3 µM C (Fig. 1). In contrast, there is no significant decline in DOC with increasing depth beyond 1000 m depth (Fig. 1), indicating that DOC exported with overturning circulation plays a minor role in supporting respiration in the ocean interior (5). Assuming a molar respiratory quotient of 0.69, the decline in DOC accounts for 19.6 ± 0.4% of the AOU within the top 1000 m (Fig. 1). This estimate represents, however, an upper limit, because the correlation between DOC and AOU is partly due to mixing of DOC-rich warm surface waters with DOC-poor cold thermocline waters (6). Removal of this effect by regressing DOC against AOU and water temperature indicates that DOC supports only 8.4 ± 0.3% of the respiration in the mesopelagic waters.