Electron Microprobe Analysis of 9th–12th Century Islamic Glass from Córdoba,Spain

Twenty‐six samples from domestic assemblages of 9th–12th century Córdoba were subjected to electron microprobe analysis. The results reveal two main compositional types. The first, encountered in 13 of the samples, seems to result from the combination of plant ashes with high‐impurity sand, and has some contemporary parallels from Syria and Egypt. The second type is a lead–soda–silica glass, encountered in a relatively high proportion of the glasses (11 of the 26 sampled), possibly formed by the addition of lead metal to existing glasses and with very few known parallels. These are among a very small number of results available to date on the chemical composition of glasses from medieval Spain, and the presence of a high proportion of lead–soda–silica glasses is particularly interesting, possibly indicating a technological practice unique to, or originating in, the western Muslim world.     

Freezing and melting behaviors of H2O‐NaCl‐CaCl2 solutions in fused silica capillaries and glass‐sandwiched films: implications for fluid inclusion studies

Fluid inclusions of the H₂O‐NaCl‐CaCl₂ system are notorious for their metastable behavior during cooling and heating processes, which can render microthermometric measurement impossible or difficult and interpretation of the results ambiguous. This study addresses these problems through detailed microscopic examination of synthetic solutions during cooling and warming runs, development of methods to enhance nucleation of hydrates, and comparison of microthermometric results with different degrees of metastability with values predicted for stable conditions. Synthetic H₂O‐NaCl‐CaCl₂ solutions with different NaCl/(NaCl + CaCl₂) ratios were prepared and loaded in fused silica capillaries and glass‐sandwiched films for microthermometric studies; pure solutions were used with the capillaries to simulate fluid inclusions, whereas alumina powder was added in the solutions to facilitate ice and hydrate crystallization in the sandwiched samples. The phase changes observed and the microthermometric data obtained in this study have led to the following conclusions that have important implications for fluid inclusion studies: (i) most H₂O‐NaCl‐CaCl₂ inclusions that appear to be completely frozen in the first cooling run to ?185°C actually contain large amounts of residual solution, as also reported in some previous studies; (ii) inability of H₂O‐NaCl‐CaCl₂ inclusions to freeze completely may be related to their composition (low NaCl/(NaCl + CaCl₂) ratios) and lack of solid particles; (iii) crystallization of hydrates, which is important for cryogenic Raman spectroscopic studies of fluid inclusion composition, can be greatly enhanced by finding an optimum combination of cooling and warming rates and temperatures; and (iv) even if an inclusion is not completely frozen, the melting temperatures of hydrohalite and ice are still valid for estimating the fluid composition.     

In situ decarboxylation of acetic and formic acids in aqueous inclusions as a possible way to produce excess CH4

Accurate reconstruction of diagenetic P‐T conditions in petroleum reservoirs from fluid inclusion data relies on valid measurements of methane concentration in aqueous inclusions. Techniques have been developed (Raman spectrometry) to provide sufficiently accurate data, assuming measured methane concentration has not been modified after aqueous inclusion entrapment. This study investigates the likelihood that organic acids derived from petroleum fluids and dissolved in formation water might suffer decarboxylation upon postentrapment heating within the fluid inclusion chamber, thereby generating excess CH₄ in the inclusions. Four different experiments were conducted in fused silica capillary capsules (FSCCs), mimicking fluid inclusions. The capsules were loaded with acetic (CH₃COOH) or formic (HCOOH) acid solution and were heated to 250°C for short durations (<72 h) in closed‐system conditions, with or without applying a fixed P_H2. Reaction products were characterized by Raman and FT‐IR spectrometry. Results indicate that decarboxylation reactions did take place, at variable degrees of progress, and that measurable excess CH₄ was produced in one experiment using acetic acid. This suggests that methane may be produced from dissolved organic acids in natural aqueous inclusions in specific situations, possibly inducing errors in the thermodynamic interpretation.     

壳聚糖/二氧化硅复合仿生膜对 碳酸盐石材的保护作用

为探讨壳聚糖/二氧化硅复合仿生膜对碳酸盐石材的保护作用,采用仿生合成技术,以十六烷基三甲基溴化铵为有机模板,能过壳聚糖调控二氧化硅颗粒的生长,在碳酸盐石材表面仿生合成得到了一层壳聚糖/二氧化硅复合保护膜,对其基本性能进行了检测评价,并利用衰减全反射红外光谱和场发射环境扫描电子显微镜表征了膜的结构形貌。实验结果表明,该膜具有优良的耐酸、耐污性能,提高了膜层的抗冻融性和耐热老化性能,并保留了石材原有的吸水性和透气性。壳聚糖/二氧化硅复合膜改善了单一二氧化硅膜的开裂问题,且该保护膜与石材基体结合紧密、膜层薄,小影响石材外脱,是一种良好的碳酸盐石材保护材料。     

Analysis of Plant Microfossils in Early European Latrine Fills from Russell,Northern New Zealand

Microfossil analysis of latrine fills from the early European (1830s) settlement of Russell, northern New Zealand, provides direct evidence for diet. Microfossils identified include pollen of maize (Zea mays), Brassicaceae (e.g., mustard, broccoli), Allium type (e.g., onion) and mint (Mentha), and starch grains of maize and potato (Solanum tuberosum). Wetland microfossils (pollen and algal spores) provide clues to source and quality of drinking water.     

The Ixtacamaxtitlán kaolinite deposit and sinter (Puebla State, Mexico): a magmatic-hydrothermal system telescoped by a shallow paleoaquifer

The Ixtacamaxtitlán hydrothermal deposit is made up of a succession, from bottom to top, of: (1) a porphyritic subvolcanic body, crosscut by quartz veins, and a stockwork with subordinate sulfides (pyrite and chalcopyrite), showing propylitic alteration haloes overprinting a previous potassic alteration event (biotitization); (2) an overlying, kaolinized lithic‐rich rhyolitic tuff; and (3) a layered opal deposit with preserved sedimentary structures. This vertical zonation, coupled with the distribution of the alteration assemblages, lead us to the interpretation of the whole as a porphyry‐type deposit grading upwards to a barren, steam‐heated, acid‐leached, kaolinite blanket with a partially preserved silica sinter on top. Both the fluid inclusion study carried out on the veins and stockwork, and the stable isotopic analyses of the kaolinized bodies, suggest the presence of two major hydrothermal events. The older event is characterized by the occurrence of hot hypersaline fluids (up to 320°C and 36 wt% NaCl equivalents), likely of magmatic origin, closely associated with the emplacement of the underlying early Miocene porphyry‐type deposit. The later event is characterized by the presence of cooler and dilute fluids (up to 140°C and 4 wt% NaCl equivalents) and by advanced argillic alteration close to the paleosurface. The calculated isotopic composition of water in equilibrium with the kaolinitic sequence plots close to and underneath the meteoric water line, partially overlapping the Los Humeros present‐day geothermal fluids. This evidence coupled with the petrographic observations suggests that steam‐heated phreatic waters altered the lithic‐rich rhyolitic tuff. This would have occurred when acid vapors, exsolved from deeper hydrothermal fluids by boiling, reached the local paleowater table and condensed, after a sector collapse that changed the system from lithostatic to hydrostatic conditions.     

唐代铁佛残块及汉代铁剑的科学分析及有机硅在其保护中的应用

章介绍了两件铁质物的科学分析及其用有机硅进行保护的过程,通过金属腐蚀速率的实验说明了有机硅可以有效减缓铁器的腐蚀速率,并结合相关资料证实了有机硅在铁质物何护中应用的可行性。     

试论沅水下游旧石器遗存

本对沅水下游17个地点的旧石器的地理埋藏、自然环境、化面貌、时代特征进行了分析,并与相邻的澧水化类群和（氵舞）水化类群进行了比较,认为这批旧石器的时代为旧石器时代早期偏晚至旧石器时代中期,属华南砾石石器传统,并指出沅水下游旧石器属于澧水化类群,兼具澧水、（氵舞）水两大化类群之间的某些过渡性特征。     

Solubility of quartz in crustal fluids: experiments and general equations for salt solutions and H2O–CO2 mixtures at 400–800°C and 0.1–0.9 GPa

The solubility of quartz has been measured in a wide range of salt solutions at 800°C and 0.5 GPa, and in NaCl, CaCl₂ and CsCl solutions and H₂O–CO₂ fluids at six additional P–T conditions ranging from 400°C at 0.1 GPa to 800°C at 0.9 GPa. The experiments cover a wide range of compositions along each binary. At P–T conditions where the density of pure water is low (0.43 g cm^?3), addition of most salts produces an enhancement of quartz solubility at low to moderate salt concentrations (salt‐in effect), although quartz solubility falls with further decrease in X_H2O. At higher fluid densities (0.7 g cm^?3 and greater), the salt‐in effect is generally absent, although this depends on both the cation present and the actual P–T conditions. The salt‐in effect is most readily produced by chloride salts of large monovalent cations, while CaCl₂ only produced a salt‐in effect at the most extreme conditions of high‐T and low‐P investigated (800°C at 0.2 GPa). Under most crustal conditions, the addition of common salts to aqueous fluids results in a lowering of quartz solubility relative to that in pure water (salt‐out effect). Comparing quartz solubility in different fluids by calculating X_H2O on the basis that all salts are fully associated under all conditions yields higher quartz solubility in solutions of monovalent salts than in solutions of divalent salts, absolute values are also influenced by cation radius. Quartz solubility measurements have been fitted to a Setchenow‐type equation, modified to take account of the separate effects of both the lowering of X_H2O and the specific effects of different salts, which are treated as arising through distinct patterns of non‐ideal behaviour, rather than the explicit formation of additional silica complexes with salt components. Quartz solubility in H₂O–CO₂ fluids can be treated as ideal, if the solvation number of aqueous silica is taken as 3.5. For this system the solubility (molality) of quartz in the binary fluid, S is related to its solubility in pure water at the same P–T conditions, S^o, by: Quartz solubility in binary salt systems (H₂O–RCl_n) can be fitted to the relationship: where salt concentration mRCl_n is expressed as molality and the exponent b has a value of 1 except under conditions where salting‐in is observed at low salt concentrations, in which case it is <1. Under most crustal conditions, the solubility of quartz in NaCl solutions is given to a good approximation by: We propose that quartz solubility in multicomponent fluids can be estimated from an extended expression, calculating X_H2O based on the total fluid composition (including dissolved gasses), and adding terms for each major salt present. Our experimental results on H₂O–NaCl–CO₂ fluids are satisfactorily predicted on this basis. An important implication of the results presented here is that there are circumstances where the migration of a fluid from one quartz‐bearing host into another, if it is accompanied by re‐equilibration through cation exchange, may lead to dissolution or precipitation of quartz even at constant P and T, with concomitant modification of the permeability structure of the deep crust.