Crystallization processes in an artificial magma: variations in crystal shape,growth rate and composition with melt cooling history     

Nelia W. Dunbar  Gary K. Jacobs  Michael T. Naney 《Contributions to Mineralogy and Petrology》1995,120(3-4):412-425

A large (4.8 m³, 1.3x10⁷ g) artificial mafic melt with a bulk composition similar to that of a basalt (but with a high CaO content of 17 wt%) was generated during a demonstration of in situ vitrification and was allowed to cool naturally. During the melting process, convection was vigorous, resulting in a chemically and thermally homogeneous melt body. Once heating was complete, the cooling rate was rapid with the temperature dropping from 1500°C to 500°C in 6 days within the interior of the 3 m diameter, 1.5 m thick body. A 20 h period of constant temperature (1140°C) observed during colling was the result of latent heat released by widespread crystallization. The final crystalline assemblage consists of diopsidic to hedenbergitic pyroxene and anorthitic feldspar, with a subordinate amount of potassic feldspar, plus a small amount of evolved glass. The compositions and proportions of phases agree well with those predicted by the MELTS thermodynamic model. Thermal and textural evidence suggest that convection within the melt ceased coincident with formation of the first crystals. Textural investigation of core samples reveals large (up to 1 cm in length) acicular diopsidic pyroxenes in a matrix of smaller feldspar and zoned pyroxene crystals (500 m in length). Crystal shape and pyroxene composition vary as a function of position within the solidified body, as a function of cooling rate. Both crystal size and degree of crystallinity are highest in the central, most slowly-cooled parts of the rock. Crystal shape is characterized by tabular, equilibrium-growth forms in the slowly-cooled areas, grading to highly skeletal, dendritic forms at the rapidly-cooled edges of the body. The pyroxene crystals are dominantly homogeneous diopside, but crystals are characterized by thin Fe-rich hedenbergitic rims. These rims were deposited when Mg in the melt was depleted by diopside growth, and melt temperature had cooled sufficiently to allow Fe-rich pyroxene growth. Crystal growth rates can be calculated based on thermal behavior of the melt, reinforced by thermodynamic modelling, and are determined to be between 10^-7 and 10^-8 cm/s in the central part of the melt. These estimates agree well with growth rates in natural systems with similar cooling rates. Pyroxene crystals that formed at a higher cooling rates are characterized by higher Al and lower Mg contents relative to tabular equilibrium crystalline forms, presumably as a result of disequilibrium melt compositions at the crystal-melt interface.New Mexico Bureau of Mines and Mineral Resources, New Mexico Institute of Mining and Technology, Socorro, NM 87801, USA  相似文献   

Pronounced occurrence of long-chain alkenones and dinosterol in a 25,000-year lipid molecular fossil record from Lake Titicaca, South America     

Kevin M. Theissen  David A. Zinniker  Robert B. Dunbar 《Geochimica et cosmochimica acta》2005,69(3):623-636

Our analysis of lipid molecular fossils from a Lake Titicaca (16° S, 69° W) sediment core reveals distinct changes in the ecology of the lake over an ∼25,000-yr period spanning latest Pleistocene to late Holocene time. Previous investigations have shown that over this time period Lake Titicaca was subject to large changes in lake level in response to regional climatic variability. Our results indicate that lake algal populations were greatly affected by the changing physical and chemical conditions in Lake Titicaca. Hydrocarbons are characterized by a combination of odd-numbered, mid- to long-chain (C₂₁-C₃₁) normal alkanes and alkenes. During periods when lake level was higher (latest Pleistocene, early Holocene, and late Holocene), the C₂₁n-alkane, and the C₂₅ and C₂₇ alkenes dominate hydrocarbon distributions and indicate contribution from an algal source, potentially the freshwater alga Botryococcus braunii. The C₃₀ 4 α-methyl sterol (dinosterol) increases sharply during the mid-Holocene, suggesting a greatly increased dinoflagellate presence at that time. Long-chain alkenones (LCAs) become significant during the early Holocene and are highly abundant in mid-Holocene samples. There are relatively few published records of LCA detection in lake sediments but their occurrence is geographically widespread (Antarctica, Asia, Europe, North America). Lake Titicaca represents the first South American lake and the first low-latitude lake in which LCAs have been reported. LCA abundance and distribution may be related to the temperature-dependent response of an unidentified algal precursor. Although the LCA unsaturation indices cannot be used to determine absolute Lake Titicaca temperatures, we suspect that the published LCA U₃₇^K unsaturation calibrations can be applied to infer relative temperatures for early to mid-Holocene time when LCA concentrations are high. Using these criteria, the U₃₇^K unsaturation indices suggest relatively warmer temperatures in the mid-Holocene. In contrast to previous speculation, lipid analysis provides little evidence of a greatly increased presence of aquatic plants during the mid-Holocene. Instead, it appears that a few algal species were dominant in the lake. Based on the dramatic rise in abundances of LCAs and dinosterol during the early to mid-Holocene, we suspect that the algal producers of these compounds rose in response to a combination of physical and chemical changes in the lake. These include temperature, salinity, and alkalinity changes that occurred as lake level dropped sharply during a multi-millennial drought affecting the Central Andean Altiplano.  相似文献   

The use of 18O/16O ratios to study the formation and chemical origin of coal     

John Dunbar  A.T Wilson 《Geochimica et cosmochimica acta》1983,47(8):1541-1543

The ${}^{18}\text{O}{}^{16}\text{O}$ ratios of some New Zealand peat, lignite and coal samples were measured and compared with those of various coal precursors (cellulose, lignin and plant resins). The results showed that the major source of oxygen in all cases (except that of high rank coal) was from cellulose with the contribution from lignin and plant resins being insignificant.  相似文献   

The Pleistocene evolution of the East Antarctic Ice Sheet in the Prydz bay region: stable isotopic evidence from ODP Site 1167     

Kevin M. Theissen  Robert B. Dunbar  Alan K. Cooper  David A. Mucciarone  Dirk Hoffmann 《Global and Planetary Change》2003,39(3-4):227-256

Ocean Drilling Program Leg 188, Prydz Bay, East Antarctica is part of a larger initiative to explore the Cenozoic history of the Antarctic Ice Sheet through direct drilling and sampling of the continental margins. In this paper, we present stable isotopic results from Ocean Drilling Program (ODP) Site 1167 located on the Prydz Channel Trough Mouth Fan (TMF), the first Antarctic TMF to be drilled. The foraminifer-based δ¹⁸O record is interpreted along with sedimentary and downhole logging evidence to reconstruct the Quaternary glacial history of Prydz Bay and the adjacent Lambert Glacier Amery Ice Shelf System (LGAISS). We report an electron spin resonance age date of 36.9±3.3 ka at 0.45 m below sea floor and correlate suspected glacial–interglacial cycles with the global isotopic stratigraphy to improve the chronology for Site 1167. The δ¹⁸O record based on planktonic (Neogloboquadrina pachyderma (s.)) and limited benthic results (Globocassidulina crassa), indicates a trend of ice sheet expansion that was interrupted by a period of reduced ice volume and possibly warmer conditions during the early–mid-Pleistocene (0.9–1.38 Ma). An increase in δ¹⁸O values after 900 ka appears to coincide with the mid-Pleistocene climate transition and the expansion of the northern hemisphere ice sheet. The δ¹⁸O record in the upper 50 m of the stratigraphic section indicates as few as three glacial–interglacial cycles, tentatively assigned as marine isotopic stages (MIS) 16–21, are preserved since the Brunhes/Matuyama paleomagnetic reversal (780 ka). This suggests that there is a large unconformity near the top of the section and/or that there may have been few extreme advances of the ice sheet since the mid-Pleistocene climate transition resulting in lowered sedimentation rates on the Prydz Channel TMF. The stable isotopic record from Site 1167 is one of the few available from the area south of the Antarctic Polar Front that has been linked with the global isotopic stratigraphy. Our results suggest the potential for the recovery of useful stable isotopic records in other TMFs.  相似文献   

Sediment type distribution in reservoirs: sediment source versus morphometry     

J. Abraham  P. M. Allen  J. A. Dunbar  S. I. Dworkin 《Environmental Geology》1999,38(2):101-110

 Bottom sediments were collected from seven Texas reservoirs to assess the spatial distribution of sediment types in reservoirs. The sediment samples were analyzed for water content, organic content, and grain-size distributions. The reservoirs are characterized by distinct water content patterns (referred to in this paper as Types I, II, and III) that reflect the lithologic units comprising their drainage area. The water content, organic content, and percent mud decreases from Type I (shale, marl) through Type II (limestone-marl-sandstone) to Type III (granite-gneiss-schist-sandstone) reservoirs. Reported elemental concentrations in the reservoir sediments are consistent with concentrations in the dominant rocks within their drainage area. While water depth accounts for part of the spatial distribution, sediment source explains the overall distribution of sediment types. Coarse-grained source rocks, multiple source rocks, and multiple tributaries which input sediment at different points contribute to an inconsistent sediment type distribution. Depending on the sediment source, sand and gravel-size sediments are present in the deeper regions of some reservoirs. This disrupts the classical morphometry (water depth, slope) controlled sediment distribution pattern (coarser sediments in shallower regions and finer sediments in deeper regions) of natural lakes. Thus, the location of tributaries and the type of sediments they carry are the dominant factors that control the sediment type distribution in reservoirs. Received: 16 June 1998 · Accepted: 24 August 1998  相似文献   

The changing role of ecohydrological science in guiding environmental flows     

M.C. Acreman  I.C. Overton  J. King  P.J. Wood  I.G. Cowx  M.J. Dunbar 《水文科学杂志》2014,59(3-4):433-450

Abstract

The term “environmental flows” is now widely used to reflect the hydrological regime required to sustain freshwater and estuarine ecosystems, and the human livelihoods and well-being that depend on them. The definition suggests a central role for ecohydrological science to help determine a required flow regime for a target ecosystem condition. Indeed, many countries have established laws and policies to implement environmental flows with the expectation that science can deliver the answers. This article provides an overview of recent developments and applications of environmental flows on six continents to explore the changing role of ecohydrological sciences, recognizing its limitations and the emerging needs of society, water resource managers and policy makers. Science has responded with new methods to link hydrology to ecosystem status, but these have also raised fundamental questions that go beyond ecohydrology, such as who decides on the target condition of the ecosystem? Some environmental flow methods are based on the natural flow paradigm, which assumes the desired regime is the natural “unmodified” condition. However, this may be unrealistic where flow regimes have been altered for many centuries and are likely to change with future climate change. Ecosystems are dynamic, so the adoption of environmental flows needs to have a similar dynamic basis. Furthermore, methodological developments have been made in two directions: first, broad-scale hydrological analysis of flow regimes (assuming ecological relevance of hydrograph components) and, second, analysis of ecological impacts of more than one stressor (e.g. flow, morphology, water quality). All methods retain a degree of uncertainty, which translates into risks, and raises questions regarding trust between scientists and the public. Communication between scientists, social scientists, practitioners, policy makers and the public is thus becoming as important as the quality of the science.