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661.
Elemental ratio data from archaeological and paleontological bone have often been used for paleoecological reconstruction, but recent studies have shown that, even when solubility profiling techniques are employed in an attempt to recover biogenic signals, bone is an unreliable material. As a result, there has been renewed interest in using enamel for such studies, as it is known to be less susceptible to diagenesis. Nevertheless, enamel is not immune from diagenetic processes, and several studies have suggested that paleoecologically relevant elements may be altered in fossil enamel. Here, we investigate Sr, Ba, Zn, and Pb compositions of enamel from South African karstic cave sites in an effort to ascertain whether or not this material provides reliable paleoecological information. We compared enamel data for mammals from three fossil sites aged 1.8-3.0 Ma, all of which are on dolomites, with data from modern mammals living on dolomitic and granitic substrates. Sr/Ca and Ba/Ca are about three times higher in enamel from modern mammals on granites than those living on dolomites, stressing the need for geologically appropriate modern/fossil comparisons. After pretreatment with dilute acid, we found no evidence of increased Sr/Ca, Ba/Ca, or Pb/Ca in fossil enamel. In contrast, Zn/Ca increased by over five times at one site (Makapansgat), but much more subtly elsewhere. Ecological patterning in Sr/Ca, Ba/Ca, and Sr/Ba ratios was also retained in fossil enamel. This study suggests that Sr/Ca, Ba/Ca, and Pb/Ca data likely preserve paleoecological information from these sites, but also demonstrates that geologically similar sites can differ in the degree to which they impart certain elements (Zn in this case) to fossils. Thus, screening is probably necessary on a site-by-site basis. Lastly, further investigation of elemental distributions in modern foodwebs is necessary before elemental ratio analysis can become a common tool for paleoecological reconstruction. 相似文献
662.
Ten to 100 meV protons from the solar flare of March 24, 1966 were observed on the University of California scintillation counter on OGO-I. The short rise and decay times observed in the count rates of the 32 channels of pulse-height analysis show that scattering of the protons by the interplanetary field was much less important in this event than in previously observed proton flares. A diffusion theory in which D = M
r
is found to be inadequate to account for the time behavior of the count rates of this event. Small fluctuations of the otherwise smooth decay phase may be due to flare protons reflected from the back of a shock front, which passed the earth on March 23. 相似文献
663.
BF3 counters on OSO-1 were used to look for solar neutrons by trying to observe a diurnal variation in count rate. No effect was observed and an upper limit was placed on the solar neutron flux at the earth of J
n < 2 × 10–3 neut/cm2/sec of 10 keV < E
n < 10 meV for the period March to May 1962. No proton-producing flares occurred during this time, so the most obvious source of solar neutrons could not be studied. The emulsion experiment of Apparao et al., flown during this period, which seemed to indicate solar neutrons has probably been misinterpreted. 相似文献
664.
This paper describes the instrumentation of an Aerobee rocket (NASA 4.95 GS) which was launched from White Sands Missile Range on May 20th 1966, to observe the Sun in the soft X-ray region. The experiment package, which was pointed at the sun by a control system stabilized about all three axes, carried two Wolter type I glancing incidence telescopes to photograph the sun in wavelength regions (determined by bandpass filters) between 3 and 75 Å, and two proportional counters to obtain flux data and rough spectral shapes in the regions 2–11 Å and 8–20 Å. The spatial resolution obtained was about 20 arc seconds. Limb brightening and polar darkening are very pronounced at the longer wavelengths. A tuft of emission was observed at the North Pole in addition to an arch-like structure on the NW limb. Several of the photographs are presented, and some preliminary results are discussed. 相似文献
665.
During the period of the IQSY, January 1964 through December 1965, the sun remained quiet, accelerating few energetic particles. There were many instances during the IQSY when lowenergy detectors on satellites and space probes registered small intensity increases. However, few of these events were associated with protons of energies exceeding 10 MeV. Moreover, the maximum intensities (E
p > 500 keV) were typically 1–8/cm2sec ster. Most of these events were below the threshold of riometer detection.The largest solar cosmic ray event observed in 1964 by polar-based riometers was that of March 16. This event was observed by 30 and 50 Mc/s riometers at McMurdo Sound, Antarctica, and Shepherd Bay, N.W.T., Canada.The largest event in 1965 occurred on February 5 and was the largest during the IQSY. It was associated with a class 2 flare at about 1750 UT, February 5. The propagation time between the sun and Earth was about one hour. This event was well observed by satellites, space probes, and riometers.This paper discusses primarily the 5 February 1965 event. Some discussion is also given to the 16 March 1964 event, other small events during the IQSY, and the recent event in March 1966. 相似文献
666.
667.
The Palaeogene Faroe Islands Basalt Group (FIBG) comprises three eruptive sequences or formations, all emplaced into a subaerial environment during the development of the extensive continental flood basalt province that stretches from East Greenland through the Faroe Islands and into the Faroe-Shetland Basin. The Beinisvørð Formation, having a tabular-classic facies architecture, is composed of a sequence of simple flows each comprising a single sheet lobe. The Beinisvørð Formation is overlain by the distinctly contrasting Malinstindur Formation that has a compound-braided facies architecture. The Enni Formation occurs at the top of the sequence and consists of a mixture of simple and compound flows with tabular-classic and compound-braided facies architectures, respectively. Surface and internal characteristics of the sheet lobes of the Beinisvørð and Enni formations indicate emplacement through inflation, which is more obvious for the tube-fed compound flows of the Malinstindur and Enni formations. The difference between the simple and compound flow sequences of the FIBG is, most likely, linked to the manner in which the lava was supplied during the eruption and the eruptive style of the volcanic system. The sheet lobes were erupted over laterally extensive areas from fissure systems which had a continuous supply of lava, which contrasts with the tube-fed compound flows which were erupted in a gradual, piecemeal manner from point-sourced, low shield volcanoes with limited areal extents. 相似文献
668.
Mo and W have been determined in five CRPG and eight ANRT geochemical reference samples by spectrophotometric - zinc dithiol procedures. Although data are lacking for adequate comparisons on most samples, our data for tungsten in GIT-IWG MA-N and GIT-IWG BE-N are very near the presently proposed values. 相似文献
669.
This paper focuses attention on the development of a numerical model of the hydro/thermo/mechanical behaviour of unsaturated clay and its consequent verification and validation. The work presented describes on-going collaboration between the Cardiff School of Engineering and Atomic Energy of Canada. The model development, which was carried out at Cardiff, can be described as being based on a mechanistic approach to coupled heat, moisture and air flow. This is then linked to a deformation analysis of the material within a ‘consolidation’ type of model. The whole is solved via the finite element method to yield a computer software code named COMPASS (COde for Modelling PArtly Saturated Soil). Some aspects of verification and validation of the model have been addressed in-house. However, the purpose of current AECL work is to provide an independent, rigorous, structured programme of validation and the paper will also explore the further validation of COMPASS within this context. © 1998 by John Wiley & Sons, Ltd. 相似文献
670.
Microbial communities in the deep subsurface 总被引:5,自引:0,他引:5
Lee R. Krumholz 《Hydrogeology Journal》2000,8(1):4-10
The diversity of microbial populations and microbial communities within the earth's subsurface is summarized in this review. Scientists are currently exploring the subsurface and addressing questions of microbial diversity, the interactions among microorganisms, and mechanisms for maintenance of subsurface microbial communities. Heterotrophic anaerobic microbial communities exist in relatively permeable sandstone or sandy sediments, located adjacent to organic-rich deposits. These microorganisms appear to be maintained by the consumption of organic compounds derived from adjacent deposits. Sources of organic material serving as electron donors include lignite-rich Eocene sediments beneath the Texas coastal plain, organic-rich Cretaceous shales from the southwestern US, as well as Cretaceous clays containing organic materials and fermentative bacteria from the Atlantic Coastal Plain. Additionally, highly diverse microbial communities occur in regions where a source of organic matter is not apparent but where igneous rock is present. Examples include the basalt-rich subsurface of the Columbia River valley and the granitic subsurface regions of Sweden and Canada. These subsurface microbial communities appear to be maintained by the action of lithotrophic bacteria growing on H2 that is chemically generated within the subsurface. Other deep-dwelling microbial communities exist within the deep sediments of oceans. These systems often rely on anaerobic metabolism and sulfate reduction. Microbial colonization extends to the depths below which high temperatures limit the ability of microbes to survive. Energy sources for the organisms living in the oceanic subsurface may originate as oceanic sedimentary deposits. In this review, each of these microbial communities is discussed in detail with specific reference to their energy sources, their observed growth patterns, and their diverse composition. This information is critical to develop further understanding of subsurface geochemical processes and to develop new approaches to subsurface remediation. Résumé La diversité des populations et des communautés microbiennes dans le sol et le sous-sol est présentée dans cet article. Les chercheurs s'interrogent fréquemment sur la diversité microbienne du sous-sol, sur les interactions entre organismes et sur les mécanismes qui permettent le maintien des communautés microbiennes souterraines. Il existe des communautés microbiennes anérobies hétérotrophes dans des grès ou dans des sédiments sableux relativement perméables, à proximité de dépôts riches en matières organiques. Ces micro-organismes semblent se maintenir grâce à la consommation de composés organiques provenant des dépôts organiques voisins. Les sources de matériel organique jouant le rôle de donneur d'électrons sont constituées par des sédiments éocènes riches en lignite situés sous la plaine littorale du Texas, les schistes riches en matières organiques du Crétacé du sud-ouest des États-Unis, ainsi que les argiles contenant des matériaux organiques et des bactéries de fermentation de la plaine littorale atlantique. En outre, il existe des communautés fortement diversifiées dans des régions où aucune source de matière organique n'existe, mais où sont présentes des roches ignées. Le sous-sol riche en basalte de la vallée de la Columbia au Canada et les régions granitiques de Suède en sont des exemples. Ces communautés microbiennes souterraines semblent se maintenir par l'action de bactéries lithotrophes se développant grâce à l'hydrogène qui est produit par réactions chimiques dans le sous-sol. Il existe d'autres communautés microbiennes de profondeur dans les sédiments profonds des océans. Ces systèmes sont souvent associés à un métabolisme anérobie et à une réduction des sulfates. La colonisation microbienne s'étend jusqu'à des profondeurs où les températures élevées limitent leur capacité de survie. Les sources d'énergie pour ces organismes vivant dans les fonds des océans peuvent être les dépôts sédimentaires océaniques. Dans cette revue, chacune des communautés microbiennes est discutée en détail en se référant spécifiquement à leurs sources d'énergie, au schéma observé de leur développement et à leur composition diversifiée. Cette information est donnée de façon critique dans le but d'améliorer la compréhension des processus géochimiques intervenant dans le sous-sol et de développer de nouvelles approches pour la dépollution souterraine. Resumen En este artículo se resume la diversidad de las poblaciones y comunidades microbianas en el subsuelo. A partir de exploraciones realizadas en el subsuelo, los científicos se están cuestionando en la actualidad aspectos relativos a la diversidad microbiana, las interacciones entre los distintos microorganismos y los mecanismos para el mantenimiento de las comunidades de microbios. Se ha comprobado la presencia de comunidades microbianas anaerobias y heterótrofas en areniscas relativamente permeables y en sedimentos arenosos ubicados cerca de depósitos ricos en materia orgánica, de la cual se alimentan. Algunas fuentes de material orgánico, que actúan como donantes de electrones, son: sedimentos del Eoceno ricos en lignito, bajo la planicie costera de Texas; pizarras del Cretácico ricas en materia orgánica, al sudoeste del país; y arcillas cretácicas con materia orgánica y bacterias fermentativas, en la llanura Atlántica. También existen comunidades microbianas de gran diversidad en rocas ígneas, aunque la fuente de materia orgánica no es tan evidente. Algunos ejemplos son la subsuperficie del valle del Río Columbia, rico en basaltos, y las regiones graníticas de Suecia y Canadá. Estas comunidades microbianas subsuperficiales se mantienen por la acción de bacterias litotrópicas, que crecen en ambiente de H2, generado en la subsuperficie. También existen comunidades microbianas a gran profundidad, como por ejemplo en los sedimentos oceánicos. Estos sistemas subsisten con un metabolismo anaerobio en un ambiente sulfato-reductor. La colonización microbiana se extiende hasta profundidades tales que las altas temperaturas limitan su supervivencia. Las fuentes de energía para estos organismos pueden ser los depósitos sedimentarios oceánicos. En este artículo se discute cada una de estas comunidades en detalle, en particular sus fuentes de energía, su esquema de crecimiento y la diversidad de su composición. Esta información es de gran interés para permitir un mayor entendimiento de los procesos geoquímicos en profundidad y para desarrollar nuevos métodos de rehabilitación. 相似文献