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1.
简评《地质辞典》中的“煤层气”词条 总被引：2，自引：0，他引：2
简要评述了《地质辞典》中“煤层气”词条释义方面存在的谬误；指出该词条作者不仅没有给读者任何正确、有用的信息，更为严重的是对煤层气资源工业价值的否定性评价阻碍了我国煤层气的研究、勘探开发进程。因此《地质辞典》再版时，应对煤层气词条进行全面修订，以免继续误导读者。 相似文献
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<正>During April 3~(rd)–14~(th),the Third International Ophiolite Workshop of the International Geoscience Programme"Diamonds and Recycled Mantle"(IGCP-649)was successfully held in Havana,Cuba(Fig.1a).After the workshop,participants participated in a field trip to the Mayarí-Baracoa ophiolites and related chromitites in 相似文献
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CH4 and CO2 fluxes from a high-cold swamp meadow and an alpine meadow on the Qinghai-Tibetan Plateau, subject to different degrees of
degradation, were measured over a 12-month period. Air temperature, soil temperature and moisture, and the depths of the water
table and thawing-freezing layer were determined. For swamp meadows, the greater the degradation, the lesser the carbon efflux.
CH4 emissions at the nondegraded swamp meadow site were 1.09–3.5 and 2.5–11.27 times greater, and CO2 emissions 1.08–1.69 and 1.41–4.43 times greater, respectively, than those from moderately and severely degraded sites. For
alpine meadows, the greater the degradation, the greater the CH4 consumption and CO2 emissions. CH4 consumption at the severely degraded alpine meadow site was 6.6–21 and 1.1–5.25 times greater, and CO2 emissions 1.05–78.5 and 1.04–6.28 times greater, respectively, than those from the nondegraded and moderately degraded sites.
The CH4 and CO2 fluxes at both sites were significantly correlated (R
2 > 0.59, P < 0.05) with air temperature, soil temperature, and topsoil (0–5 cm depth) moisture, indicating these to be the main environmental
factors affecting such fluxes. 相似文献
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食盐析出实验对盐湖盆地沉积研究的启示 总被引：1，自引：0，他引：1
将物理模拟实验结果与地震、岩芯资料相结合,对东濮凹陷盐岩沉积的古地理位置、成因机制提出新的认识。研究认为:洼陷带的边缘、中央隆起带等浅水部位是盐岩沉积较早的部位,可以沉积厚度大、粒度小的单盐层,而靠近湖盆中心,矿物结晶时间充分,沉积的盐岩粒度大,单盐层厚度可大可小,甚至可以缺失,盐岩沉积的古地理位置受古盐度影响明显;盐湖盆地绝大多部分地区,湖水有一定深度时便已形成湖底盐层,湖水变浅时盐层已具备一定厚度,保证了其下部泥页岩的还原环境,盐岩沉积后基本保持了原有的构造形态,其上可以再次接受泥页岩沉积;湖盆边缘的渗滤带在湖水退去以后仍可以沉积盐岩,该处盐层最薄、粒度细小,下部地层常见氧化环境标志。 相似文献
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Lucinid bivalves dominate the infauna of tropical seagrass sediments. While the effect of seagrass on lucinids has been studied,
the reverse effect has largely been ignored. Lucinids can alter porewater chemistry (i.e., increase porewater nutrients by
suspension feeding and decrease porewater sulfides by oxygen introduction and bacterial oxidation), which can potentially
change seagrass productivity and growth morphology. To observe correlations between porewater chemistry and lucinid presence,
a field survey and laboratory microcosm experiment were conducted. Survey sampling sites with lucinids had significantly lower
sulfide and higher ammonium concentrations than sampling sites without lucinids. There was no difference in phosphate concentration
among sampling sites. Both lucinid species used in the microcosm experiment (Ctena orbiculata andLucinesca nassula) significantly lowered sulfide concentrations in the sediment porewater. Microcosm and field survey results were incorporated
into a sulfide budget. In seagrass sediments, lucinids remove 2–16% of the total sulfide produced. Sulfide is a major stressor
to both plants and animals in Florida Bay sediments; this removal may be important to maintaining seagrass productivity and
health. Oxygen introduction into sediments byC. orbiculata was estimated in a dye experiment.C. orbiculata were added to small tubes containing sieved mud and incubated in a bath of seawater with a Rhodamine WT. Rhodamine WT accumulation
in the sediment was measured. A first order estimate showed that oxygen introduction can account for less than 5% ofC. orbiculata sulfide removal. 相似文献
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Broad iron Κα emission with a characteristic two-peaked profile is observed in most Seyfert galaxies in the X-ray. We have calculated the profiles of such lines emitted by an accretion disk in a Schwartzschild metric. The dependence of the temperature distribution in the disk on the line shape is demonstrated. All the calculations include general relativistic effects. The disk material is assumed to move in circular geodesics in the equatorial plane. The line profile is extremely complex, even in a traditional model for the radial temperature distribution, complicating interpretation of the observational data. 相似文献
11.
A standing wave in front of a seawall may reach a height more than twice of its incident component. When excess pore pressure occurs, it may even induce seabed instability, hence endangering the structure. This issue was studied previously using only linear wave theory. In this paper, standing‐wave theory to a second‐order approximation is applied, in order to demonstrate the differences between these two solutions. The spatial and temporal variations in the instantaneous pore pressure are first calculated, in addition to their vertical distributions. The effects of wave height, water depth and the degree of soil saturation on pore pressure distributions are then discussed, followed by the net pore pressure averaged over one wave cycle. The results suggest the existence of a residual pore pressure in the seabed and its net pore pressure can be used to estimate the wave‐induced liquefaction potential in a soil column. It also indicates that, in deep water, the second‐order solution predicts that a negative pore pressure at an antinode which may be greater than a positive pressure. Overall, the second‐order solution is found to agree better with the experimental results of the pore pressures available, compared to the linear solution. Copyright © 2000 John Wiley & Sons, Ltd. 相似文献
12.
《Resource Geology》2018,68(3):209-226
Shin‐Otoyo, Suttsu, Teine, Date, Chitose, and Koryu are sites rich in precious and base metal Miocene–Pleistocene epithermal deposits, and located in southwestern Hokkaido, Japan. The deposits are predominantly hosted by the Green Tuff Formation of Middle Miocene age. Ore petrographic study of these deposits shows the occurrence of variable quantities of Cu–As–Sb–Ag–Bi–Pb–Te sulfosalt minerals. Determination of mineralogical and chemical compositions of the sulfosalt minerals was undertaken to elucidate the time and spatial changes of the sulfide‐sulfosalt minerals. Various types of sulfosalt minerals identified from gold–silver and base metal quartz–sulfide veins represented some sulfosalt mineralization phases, such as the Cu–Fe–Sn–S phase of mawsonite and stannite; Cu–(As,Sb)–S phase of tetrahedrite–tennantite and luzonite–famatinite series minerals; (Cu,Ag)–Bi–Pb–S phase of emplectite, pavonite, friedrichite, aikinite, and lillianite–gustavite series minerals; (Ag,Cu)–(As,Sb)–S phase of proustite–pyrargyrite and pearceite–polybasite series minerals; and Bi–Te–S phase of tetradymite and kawazulite minerals. There are some trends in the paragenetic sequence of sulfosalt mineralization in southwestern Hokkaido (in complete or partial) as follows: sulfide → Cu–Fe–Sn–S → (Cu,Ag)–Bi–Pb–S → (Bi–Te–S) → Cu–(As,Sb)–S → ([Ag,Cu]–[As,Sb]–S). The formation of sulfosalt minerals is characterized by the introduction of some elements such as Sn, Bi, and Te at an earlier stage and an increase or decrease of some elements such as As and Sb, followed by the introduction of Ag at the later stage of ore mineral paragenesis sequence. Mineral composition of the Chitose and Koryu deposits are slightly different from those of Shin‐Otoyo, Suttsu, Teine, and Date due to their lack of Sn (tin) and Bi (bismuth) mineralization. The variable concentrations and relationships are not simply with redistributed trace elements from the original sulfide minerals of chalcopyrite, pyrite, galena, and sphalerite. Some heavier elements were also introduced during the replacement reaction, which is consistent with the occurrence of their associated minerals. 相似文献
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Kevin St. Martin 《Geoforum》2006,37(2):169-184
The discourse of fisheries science and management displaces community and culture from the essential economic dynamic of fisheries. The goal of this dominant discourse is to enclose fisheries, to constitute them as within the singular and hegemonic economy of capitalism. Alternative economies, such as those based on the presence of community, are always seen as either existing before or beyond the dominant economic formation. The category of community is, nevertheless, being incorporated into contemporary fisheries science and management where it has the potential to disrupt the ontological foundations of the current management regime. To avoid disruption, community is situated such that it is the domain of anthropology while the essential economic dynamic of fisheries remains the purview of fisheries bioeconomics. Community can be identified, documented, and analyzed but always only as a site of economic impact and never as a constituent of the economic itself. Curiously, this disciplining of community has a literal geographic dimension: the discursive domain of bioeconomics corresponds to the spatial domain of fisheries resources themselves while that of fisheries social science/anthropology corresponds to the terrestrial locations where fishers reside. Fishing ports become the place of community while the actual common property resource remains the site where the essential economic dynamic reigns uncompromised. 相似文献
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A new version of the STRUCTON (2009) computer model is proposed for the simulation of the molecular mass distributions (MMD)
characterizing the diversity of anions in silicate melts depending on their polymerization and temperature. In contrast to
earlier versions, the new version of the model accounts for disproportionation reactions of Q
n
species and makes use of their proportions in the statistical simulations of the origin of real Si-O complexes. The new potentialities
of the STRUCTON program package are illustrated by its application to studying the structural-chemical characteristics of
melts in the Na2O-SiO2 system along its liquidus line, including the points of eutectics and phase transitions at 0.333 ≤ $
N_{SiO_2 }
$
N_{SiO_2 }
< 0.500. This problem is solved with the use of a temperature-composition dependence of polymerization constants K
p
Na in the Toop-Samis approximation. The variations in K
p
Na were proved to be as large as three orders of magnitude due to both the temperature effect at a constant composition and
the composition effect at a constant temperature. The results of the MMD simulations on the liquidus show that the concentration
of the SiO44− ion strongly decreases, and the proportion of chain species increases compared to those at a stochastic distribution. The
concentration of the Si2O76− anion reaches its maximum (∼42%) at 40 mol % in the liquid, i.e., the composition of Na6Si2O7. At $
N_{SiO_2 }
$
N_{SiO_2 }
> 0.40, this ion dominates over the SiO44− monomer. More silicic melts with $
N_{SiO_2 }
$
N_{SiO_2 }
≥ 0.45, are dominated by (Si
n
O3n
)3n− ring species, and the concentrations of these species are related as (Si3O9)6− > (Si4O12)8− > (Si5O15)10−. The maximum concentration of these flat rings also occurs near the composition of stoichiometric metasilicate with Si/O
= 0.333. The comparison of the dependence of the average size of anions i
av and the average number of their species on depolymerization indicates that a change in the proportion of Q
n
species in melt at decreasing temperature results in structural restyling and an increase in the average size of Si-O complexes.
The average number of anion species thereby decreases compared to that in a stochastic MMD. The results presented in this
publication direct the progress in the thermodynamic theory of silicate melts to a new avenue that makes use of the capabilities
and advantages of the ion-polymer model, the theory of associated solutions, spectroscopic data, and the experimental study
of variations in oxide activities depending on composition and temperature. 相似文献
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Bernard Hallet 《Quaternary Research》2003,59(2):279-280
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Density measurements on nine liquids in the CaCO3–Li2CO3–Na2CO3–K2CO3 quaternary system were performed at 1 bar between 555 and 969 °C using the double-bob Archimedean method. Our density data on the end-member alkali carbonate liquids are in excellent agreement with the NIST standards compiled by Janz (1992). The results were fitted to a volume equation that is linear in composition and temperature; this model recovers the measured volumes within experimental error (±0.18% on average, with a maximum residual of ±0.50%). Our results indicate that the density of the CaCO3 component in natrocarbonate liquids is 2.502 (±0.014) g/cm3 at 800 °C and 1 bar, which is within the range of silicate melts; its coefficient of thermal expansion is 1.8 (±0.5)×10–4 K–1 at 800 °C. Although the volumes of carbonate liquids mix linearly with respect to carbonate components, they do not mix linearly with silicate liquids. Our data are used with those in the literature to estimate the value of
in alkaline silicate magmas (20 cm3/mol at 1400 °C and 20 kbar), where CO2 is dissolved as carbonate in close association with Ca. Our volume measurements are combined with sound speed data in the literature to derive the compressibility of the end-member liquids Li2CO3, Na2CO3, and K2CO3. These results are combined with calorimetric data to calculate the fusion curves for Li2CO3, Na2CO3, and K2CO3 to 5 kbar; the calculations are in excellent agreement with experimental determinations of the respective melting reactions.Editorial responsibility: I Carmichael 相似文献