985 resultados para Argon atmospheres
Resumo:
A production of low velocity and monoenergetic atomic beams would increase the resolution in spectroscopic studies and many other experiments in atomic physics. Laser Cooling uses the radiation pressure to decelerate and cool atoms. The effusing from a glow discharge metastable argon atomic beam is affected by a counterpropagating laser light tuned to the cycling transition in argon. The Zeeman shift caused by a spatially varying magnetic field compensates for the changing Doppler shift that takes the atoms out of resonance as they decelerated. Deceleration and velocity bunching of atoms to a final velocity that depends on the detuning of the laser relative to a frequency of the transition have been observed. Time-of-Flight (TOF) spectroscopy is used to examine the velocity distribution of the cooled atomic beam. These TOF studies of the laser cooled atomic beam demonstrate the utility of laser deceleration for atomic-beam "velocity selection".
Resumo:
This study evaluated the degree of conversion (DC%) of one experimental and different brands of composite resins light-cured by two light sources (one LED and one argon laser). The percentage of unreacted C = C was determined from the ratio of absorbance intensities of aliphatic C = C (peak at 1637 cm−1) against internal standards before and after curing: aromatic C–C (peak at 1610 cm−1) except for P90, where %C = C bonds was given for C–O–C (883 cm−1) and C–C (1257 cm−1). ANOVA and Tukey’s test revealed no statistically significant difference among Z350 (67.17), Z250 (69.52) and experimental (66.61 ± 2.03) with LED, just among them and Evolu-X (75.51) and P90 (32.05) that showed higher and lower DC%, respectively. For the argon laser, there were no differences among Z250 (70.67), Z350 (69.60), experimental (65.66) and Evolu-X (73, 37), however a significant difference was observed for P90 (36.80), which showed lowest DC%. The light sources showed similar DC%, however the main difference was observed regarding the composite resins. The lowest DC% was observed for the argon laser. P90 showed the lowest DC% for both light-curing sources.
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The Arctic Ocean and Western Antarctic Peninsula (WAP) are the fastest warming regions on the planet and are undergoing rapid climate and ecosystem changes. Until we can fully resolve the coupling between biological and physical processes we cannot predict how warming will influence carbon cycling and ecosystem function and structure in these sensitive and climactically important regions. My dissertation centers on the use of high-resolution measurements of surface dissolved gases, primarily O2 and Ar, as tracers or physical and biological functioning that we measure underway using an optode and Equilibrator Inlet Mass Spectrometry (EIMS). Total O2 measurements are common throughout the historical and autonomous record but are influenced by biological (net metabolic balance) and physical (temperature, salinity, pressure changes, ice melt/freeze, mixing, bubbles and diffusive gas exchange) processes. We use Ar, an inert gas with similar solubility properties to O2, to devolve distinct records of biological (O2/Ar) and physical (Ar) oxygen. These high-resolution measurements that expose intersystem coupling and submesoscale variability were central to studies in the Arctic Ocean, WAP and open Southern Ocean that make up this dissertation.
Key findings of this work include the documentation of under ice and ice-edge blooms and basin scale net sea ice freeze/melt processes in the Arctic Ocean. In the WAP O2 and pCO2 are both biologically driven and net community production (NCP) variability is controlled by Fe and light availability tied to glacial and sea ice meltwater input. Further, we present a feasibility study that shows the ability to use modeled Ar to derive NCP from total O2 records. This approach has the potential to unlock critical carbon flux estimates from historical and autonomous O2 measurements in the global oceans.
Resumo:
Volcanic rocks recovered from the Japan Sea during ODP Legs 127 and 128 were analyzed by 40Ar-39Ar whole-rock stepwise-heating experiments. All three experiments on samples from Site 795 in the Japan Basin revealed disturbed age spectra, but they are consistent with crystallization ages of 15 to 25 Ma for the samples. At Site 797 in the Yamato Basin, three of the five samples showed plateau ages of 18-19 Ma. At Site 794 in the northern Yamato Basin, three of the five samples revealed concordant age spectra of 20-21 Ma. The radiometric age results are consistent with the estimated ages for the oldest sediments at Site 797 based on the biostratigraphy, but are significantly older than those of the oldest sediments at Site 794. However, the radiometric ages are concordant with previously inferred ages for the formation of the Japan Sea floor based on radiometric age data from dredged igneous rocks from the Japan Sea. The present results indicate that formation of the Japan Sea floor started at least 19-20 Ma ago and give more precise age constraints.
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A series of K-Ar dates from Mt Giluwe volcano is reported and its relevance to the Quaternary history of the volcano is discussed. The period between about 380 000 and 220 000 years BP seems to have been one of major volcanic activity. During the volcanic activity there were periods of ice cover probably of short duration. The oldest evidence of glacial action predates a lava flow dated at between 340 000 and 380 000 years. At about 290 000 years an ice cap of a thickness of at least 100 m covered the summit area and one or a series of subglacial eruption(s) led to the formation of palagonitic breccia. This event was probably associated with a complete melting of the ice since it was followed almost immediately by the eruption of a thick sequence of normal lava flows which range in age from about 289 000 years to about 220 000 years. Subsequent volcanic activity was less significant and no dates are available on this.
Resumo:
Variations of global and regional silicate weathering rates and paleo-ocean circulation patterns are estimated by using radiogenic isotope records, but the effects of changes in provenance are generally ignored. Here sediment provenance has been constrained through the use of Ar-Ar ages for individual detrital minerals from the Labrador Sea, which can be compared directly to the radiogenic isotope compositions from the same core material. Dramatic changes in the radiogenic isotope composition of North Atlantic Deep Water through the Quaternary Period are shown to reflect discrete changes in both sources and weathering processes accompanying Northern Hemisphere glaciation. Changes in the different radiogenic isotope systems reflect the influence of source, physical weathering, and chemical weathering, and not simply changes in the underlying weathering rate or ocean circulation patterns that are typically inferred.
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Structural-petrologic and isotopic-geochronologic data on magmatic, metamorphic, and metasomatic rocks from the Chernorud zone were used to reproduce the multistage history of their exhumation to upper crustal levels. The process is subdivided into four discrete stages, which corresponded to metamorphism to the granulite facies (500-490 Ma), metamorphism to the amphibolite facies (470-460 Ma), metamorphism to at least the epidote-amphibolite facies (440-430 Ma), and postmetamorphic events (410-400 Ma). The earliest two stages likely corresponded to the tectonic stacking of the backarc basin in response to the collision of the Siberian continent with the Eravninskaya island arc or the Barguzin microcontinent, a process that ended with the extensive generation of synmetamorphic granites. During the third and fourth stages, the granulites of the Chernorud nappe were successively exposed during intense tectonic motions along large deformation zones (Primorskii fault, collision lineament, and Orso Complex). The comparison of the histories of active thermal events for Early Caledonian folded structures in the Central Asian Foldbelt indicates that active thermal events of equal duration are reconstructed for the following five widely spiced accretion-collision structures: the Chernorud granulite zone in the Ol'khon territory, the Slyudyanka crystalline complex in the southwestern Baikal area, the western Sangilen territory in southeastern Tuva, Derbinskii terrane in the Eastern Sayan, and the Bayankhongor ophiolite zone in central Mongolia. The dates obtained by various isotopic techniques are generally consistent with the four discrete stages identified in the Chernorud nappe, whereas the dates corresponding to the island-arc evolutionary stage were obtained only for the western Sangilen and Bayankhongor ophiolite zone.
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During Ocean Drilling Program (ODP) Leg 180, 11 sites were drilled in the vicinity of the Moresby Seamount to study processes associated with the transition from continental rifting to seafloor spreading in the Woodlark Basin. This paper presents thermochronologic (40Ar/39Ar, 238U/206Pb, and fission track) results from igneous rocks recovered during ODP Leg 180 that help constrain the latest Cretaceous to present-day tectonic development of the Woodlark Basin. Igneous rocks recovered (primarily from Sites 1109, 1114, 1117, and 1118) consist of predominantly diabase and metadiabase, with minor basalt and gabbro. Zircon ion microprobe analyses gave a 238U/206Pb age of 66.4 ± 1.5 Ma, interpreted to date crystallization of the diabase. 40Ar/39Ar plagioclase apparent ages vary considerably according to the degree to which the diabase was altered subsequent to crystallization. The least altered sample (from Site 1109) yielded a plagioclase isochron age of 58.9 ± 5.8 Ma, interpreted to represent cooling following intrusion. The most altered sample (from Site 1117) yielded an isochron age of 31.0 ± 0.9 Ma, interpreted to represent a maximum age for the timing of subsequent hydrothermal alteration. The diabase has not been thermally affected by Miocene-Pliocene rift-related events, supporting our inference that these rocks have remained at shallow and cool levels in the crust (i.e., upper plate) since they were partially reset as a result of middle Oligocene hydrothermal alteration. These results suggest that crustal extension in the vicinity of the Moresby Seamount, immediately west of the active seafloor spreading tip, is being accommodated by normal faulting within latest Cretaceous to early Paleocene oceanic crust. Felsic clasts provide additional evidence for middle Miocene and Pliocene magmatic events in the region. Two rhyolitic clasts (from Sites 1110 and 1111) gave zircon 238U/206Pb ages of 15.7 ± 0.4 Ma and provide evidence for Miocene volcanism in the region. 40Ar/39Ar total fusion ages on single grains of K-feldspar from these clasts yielded younger apparent ages of 12.5 ± 0.2 and 14.4 ± 0.6 Ma due to variable sericitization of K-feldspar phenocrysts. 238U/206Pb zircon, 40Ar/39Ar K-feldspar and biotite total fusion, and apatite fission track analysis of a microgranite clast (from Site 1108) provide evidence for the existence of a rapidly cooled 3.0 to 1.8 Ma granitic protolith. The clast may have been transported longitudinally from the west (e.g., from the D'Entrecasteaux Islands). Alternatively, it may have been derived from a more proximal, but presently unknown, source in the vicinity of the Moresby Seamount.
Resumo:
Although various models have been proposed to explain the origin of manganese nodules (see Goldberg and Arrhenius), two major hypotheses have received extensive attention. One concept suggests that manganese nodules form as the result of interaction between submarine volcanic products and sea water. The common association of manganese nodules with volcanic materials constitutes the main evidence for this theory. The second theory involves a direct inorganic precipitation of manganese from sea water. Goldberg and Arrhenius view this process as the oxidation of divalent manganese to tetravalent manganese by oxygen under the catalytic action of particulate iron hydroxides. Manganese accumulation by the Goldberg and Arrhenius theory would be a relatively slow and comparatively steady process, whereas Bonatti and Nayudu believe manganese nodule formation takes place subsequent to the eruption of submarine volcanoes by the acidic leaching of lava.
Resumo:
Il CTBT (Trattato di Bando Complessivo dei Test Nucleari) è un accordo multilaterale tra Stati, stilato nel 1996, che impone il divieto assoluto di effettuare esplosioni di tipo nucleare, sia per scopi civili che per scopi militari, in qualsiasi ambiente. Esso prevede l'istituzione di un sistema di verifica e monitoraggio che si prefigge lo scopo di rilevare tempestivamente se in una qualsiasi parte del mondo sia stato clandestinamente effettuato un test. Tra le varie tecniche utilizzate, la più decisiva per l'identificazione di un'esplosione è data dal monitoraggio di radionuclidi, che permette di fare ipotesi su di un eventuale evento illecito di origine nucleare se in una certa regione si rileva la presenza nell'ambiente di particolari isotopi radioattivi in quantità anomale. Attualmente, il metodo più efficace consiste nell'eventuale identificazione della presenza di quattro radioisotopi di gas nobili, ovvero xeno-131m, xeno-133, xeno-133m e xeno-135. Di recente, però, gli esperti hanno cominciato a valutare l'ipotesi di effettuare misurazioni anche di un altro radioisotopo di gas nobili, ovvero l'argon-37. L'efficacia nell'utilizzo di quest'ultimo è superiore a quella che caratterizza il monitoraggio dello xeno, anche se il motivo per cui il metodo di rilevazione dell'argon non è ancora sfruttato è dato dall'estrema difficoltà che la sua misurazione comporta. Obiettivo di questo lavoro è proprio quello di analizzare le potenzialità dell'utilizzo di tale radioisotopo dell'argon per gli scopi di verifica del CTBT, di descrivere l'attuale stato dell'arte delle tecnologie disponibili per la sua misurazione e di valutare quantitativamente il fondo di argon-37 naturalmente presente, in modo da stabilire i criteri con cui si possa dire se le quantità rilevate siano compatibili con la normale presenza di tale radioisotopo oppure se siano senza dubbio dovute a un'avvenuta esplosione.