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201.
古—中生代之交的全球变化与生物效应 总被引:9,自引:0,他引:9
古—中生代之交是显生宙以来最大的一次生物绝灭期 ,其形成机制一直是地学界长期探讨的热点课题之一。地史重大转折期是地球内、外各圈层长期作用下 ,各种量变达到阀值 ,加之可能的外因激化 ,在短时间内以连锁反应形式相继质变 ,形成了全球变化 (包括生物绝灭 )的地球突变期。文中从可能的外因 (外星体撞击事件 )及内因 (岩石圈的变化 ,地球表层的变化和生物圈的变化 )两个方面探讨了古—中生代之交的全球变化与生物效应 相似文献
202.
25~75℃酸性NaCl溶液中方铅矿的溶解动力学 总被引:4,自引:0,他引:4
在25~75℃、pH=0.43~2.45的1mol/LNaCl溶液中进行了方铅矿的溶解动力学实验。发现在远平衡条件下,方铅矿的溶解速率r与氢离子活度犤H+犦呈线性关系,溶解速率方程(速率定律)为:r=k犤H+犦,即对H+而言,溶解反应为一级。其中速率常数k为2.344×10-7mol/m2·s(25℃)、1.380×10-6mol/m2·s(50℃)、7.079×10-6mol/m2·s(75℃)。溶解反应的活化能为43.54kJ/mol,方铅矿的溶解机理为表面化学反应,速率决定步骤为表面配合物的离解。 相似文献
203.
204.
A total of four times of rhabdosome complication events, i.e., the lateral branching of graptolite stipes during the Late Middle Ordovician, the secondary branching of graptolite stipes at the earliest Upper Ordovician, the early Qiantangjiangian of Upper Ordovician and the middle Qiantangjiangian, respectively, is discussed in this paper. These events and other adaptation events demonstrate close relationships between a diverse graptolite fauna and sea level changes, and consequently can be employed to study sea level fluctuations. It is safe to conclude that the complication of rhabdosome started at the maximum flooding surface (MFS) and terminated at the beginning of regression. 相似文献
205.
As a legacy of the centrally planned economy, the economies in transition of Central and Eastern Europe (CEE) have a unique
potential to reduce their greenhouse gas emissions through the improvement in their high energy intensities. Since much of
this `low-hanging fruit' in energy-efficiency improvements can be highly cost-effective, many developed countries facing difficulties
in meeting their greenhouse gas (GHG) emission targets domestically are eager to find such opportunities in the CEE region.
Therefore, studies analysing the potentials and costs of carbon dioxide reduction through technology improvement in the region
have come into the limelight. While there are a few excellent studies in the region aimed at analysing climate change abatement
potentials, they all embark on different assumptions, methodologies and boundary conditions. It is hence difficult, if not
impossible, to compare and analyse the results of these studies across different authors, countries or time horizons. Consequently,
the purpose of this paper is to place four leading studies on GHG mitigation through technology improvement from the CEE region
into an internationally comparable framework. Four studies were selected from three countries, Poland, Hungary and Estonia,
which are all the results of major national and international efforts to assess costs and potentials of GHG reduction. The
paper places their assumptions, methods and final results into a framework which enables policy-makers and project designers
to compare these across geographical and technological boundaries. Since other studies from around the globe have been analysed
in this framework in the literature, this paper provides a vehicle for the findings of these four studies to be compared to
others worldwide. In addition, the paper highlights a few areas where similar studies to be completed in the future in the
region may be enhanced by incorporating features used in GHG mitigation research in other parts of the world.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
206.
Mark E. Hodson 《Chemical Geology》2002,190(1-4):91-112
Far-from-equilibrium batch dissolution experiments were carried out on the 2000–500, 500–250, 250–53 and 53–2 μm size fractions of the mineral component of the B horizon of a granitic iron humus podzol after removal of organic matter and secondary precipitates. The different size fractions were mineralogically and chemically similar, the main minerals present being quartz, alkali and plagioclase feldspar, biotite and chlorite. Specific surface area increased with decreasing grain size. The measured element release rates decreased in the order 53–2>>>2000–500>500–250>250–53 μm. Surface area normalised element release rates from the 2000–500, 500–250 and 250–53 μm size fractions (0.6–77×10−14 mol/m2/s) were intermediate between literature reported surface area normalised dissolution rates for monomineralic powders of feldspar (0.1–0.01×10−14 mol/m2/s) and sheet silicates (100×10−14 mol/m2/s) dissolving under similar conditions. Element release rates from the 53–2 μm fraction (400–3000×10−14 mol/m2/s) were a factor of 4–30 larger than literature reported values for sheet silicates. The large element release rate of the 53–2 μm fraction means that, despite the small mass fraction of 53–2 μm sized particles present in the soil, dissolution of this fraction is the most important for element release into the soil. A theoretical model predicted similar (within a factor of <2) bulk element release rates for all the mineral powders if observed thicknesses of sheet silicate grains were used as input parameters. Decreasing element release rates with decreasing grain size were only predicted if the thickness of sheet silicates in the powders was held constant. A significantly larger release rate for the 53–2 μm fraction relative to the other size fractions was only predicted if either surface roughness was set several orders of magnitude higher for sheet silicates and several orders of magnitude lower for quartz and feldspars in the 53–2 μm fraction compared to the other size fractions or if the sheet silicate thickness input in the 53–2 μm fraction was set unrealistically low. It is therefore hypothesised that the reason for the unpredicted large release rate from the 52–3 μm size fraction is due to one or more of the following reasons: (1) the greater reactivity of the smaller particles due to surface free energy effects, (2) the lack of proportionality between the BET surface area used to normalise the release rates and the actual reactive surface area of the grains and, (3) the presence of traces quantities of reactive minerals which were undetected in the 53–2 μm fraction but were entirely absent in the coarser fractions. 相似文献
207.
We studied the dissolved silica cycle in the water column of the North basin of Lake Lugano, Switzerland/Italy. Lake Lugano is a meromictic, eutrophic lake, permanently stratified below 100-m depth. A one-box model was used to calculate a silica mass-balance over 1993, based on various lake measurements, such as sediment traps, sediment cores, water analysis and biota countings. We found that the North basin of Lake Lugano is at steady state as far as dissolved silica is concerned. The primary source of dissolved silica in the lake is river input (about 80%), with diffusion from bottom sediments and groundwater input also playing a role. Atmospheric input is negligible. The main export of dissolved silica occurs via biogenic uptake by diatoms and final burial of their frustules in the bottom sediment. Loss of dissolved silica through the lake outflow only represents 15% of the total output. Of the total amount of Si exported to the lake bottom through diatom sinking, less than 20% is re-supplied to the surface water by diffusion. Thus, the lake acts as an important permanent sink for silica. The long residence time of dissolved silica in the lake (7 years) is related to the strong physical stratification of the lake. Only about 10% of the standing stock are available to phytoplankton uptake. 相似文献
208.
209.
Marianne Font Jean-Louis Lagarde Daniel Amorese Jean-Pierre Coutard Jean-Claude Ozouf 《Comptes Rendus Geoscience》2002,334(3):171-178
The degradation of the Jobourg fault-scarp occurred by cryoclastic processes in a periglacial environment during a part of Quaternary time. An attempt of quantification indicates a bulk scarp erosion of about 39 m3 m?2, while the head accumulated at the bottom of the fault scarp only represents 4.6 m3 m?2. To cite this article: M. Font et al., C. R. Geoscience 334 (2002) 171–178. 相似文献
210.