Study of physical and chemical properties of vitrinites. Inferences on depositional and coalification controls

A detailed study of petrological, geochemical, textural and coking properties was carried out on vitrains from the Puertollano, Blanzy–Montçeau, Asturias and Teruel. The objective was to determine in depth the physical and chemical properties of a series of natural and pure vitrinites of different rank, and the influence that the sedimentary and post-sedimentary conditions had on them. It is demonstrated that although vitrains are almost entirely made up of the huminite/vitrinite maceral group they have a different composition, thermal behaviour and physical properties. Thus, geochemical and textural properties of Blanzy–Montçeau vitrains can be considered to be representative of the telinite, the major component in both samples (75% vol.) at the beginning of the bituminization stage (subbituminous/high volatile C bituminous coals). The characteristics of the Puertollano vitrains described here can also be attributed to the telocollinite (>80% vol.) for the high volatile C bituminous coal. Variations in physico-chemical properties between Puertollano and Blanzy–Montçeau vitrains are due to the differences in the initial composition of organic matter. Slight differences (i.e., bed moisture content or porosity) between vitrains from the two coal seams in the same basin can be attributed to their stratigraphic position. Several parameters such as S₂, HI, oil and extraction yield and fluorescent properties suggest that the Puertollano and Blanzy–Montçeau vitrains have a lower hydrocarbon potential. The relationships between geochemical and textural properties make it possible to distinguish between ‘normal' and perhydrous vitrains. The two different hydrogen-enrichment processes that occur in vitrains from the Teruel and Asturias basins can be distinguished from the extraction yield data.     

Potential Impact of Production Chemicals on the Toxicity of Produced Water Discharges from North Sea Oil Platforms

Production chemicals are used on offshore oil production platforms to prevent corrosion and scale formation, and to assist oil–water separation. A proportion of these chemicals may enter the marine environment via the produced water discharge. This study investigated the potential impact of 11 oilfield production chemicals on the toxicity of the produced water discharge. The Microtox® system was used for toxicity assessment of the chemicals, both directly in aqueous preparations and following their partitioning between oil (crude and low toxicity mineral base oil) and North Sea brine. For the majority of the chemicals tested, the toxicity of the aqueous phase to the test organism following partitioning against crude oil, was not significantly altered by the presence of process chemicals when used in their normal field dosage concentrations. However, there was evidence that certain chemicals could increase the partitioning of oil components into the aqueous phase by an order of magnitude, when applied at high dosage concentrations.     

Multiple Discriminant Analysis of Marine Sediment Data

A multivariate statistical approach was used in the analysis of inter-relationships among marine benthic infaunal structure, physical and chemical characteristics of sediment samples and toxicity data derived from laboratory tests at 16 locations in shallow, inshore waters of Hong Kong. The method involved classification (cluster analysis using the Bray–Curtis similarity index) and ordination (multi-dimensional scaling) of infaunal patterns and the use of multiple discriminant analysis to relate groupings of the locations to the selected environmental and toxicity data. Analysis of the combined sediment physical, biological, chemical and toxicity dataset by stepwise multiple discriminant analysis allowed identification of those variables most sensitive for discriminating location groups. The use of multiple discriminant analysis in sediment quality characterization was evaluated against the Sediment Quality Triad approach and other statistical techniques.     

气象因素与急性脑血管病的相关研究

经10年对照分析,提出了武汉地区气象因素对急性脑血管病影响规律性和预测急性脑血管的4项危险因素,即：（1）相对湿度大于74%;（2）气压在1017.5 hPa左右;（3）低温的冬季;（4）每年1、5、10月3个月（特别是1月份）为高发月,并通过1991～1995年5年的病例加以验证,可信性达80%～90%。     

四种重金属对海洋钙质角毛藻的毒性

研究了Ｈｇ＾２＋、Ｃｕ＾２＋、Ｚｎ＾２＋、Ｃｄ＾２＋４种重金属,其单一及４种混合对海洋单胞藻钙质角毛藻Ｃｈａｅｔｏｃｅｒｏｓ ｃａｌｃｕｔｒａｎｓ的毒性效应,结果表明：单一的重金属毒性强于４种重金属混合,而且不同重金属对单胞藻的毒性效应有所不同,其毒性均Ｈｇ＾２＋〉Ｃｕ＾２＋〉Ｚｎ＾２＋〉Ｃｄ＾２＋。     

Surfactant components of marine organic matter as agents for biogeochemical fractionation and pollutant transport via marine aerosols

The role of surfactant organic matter in marine aerosol production has been studied under conditions in which there is a large coverage of whitecaps on the sea surface. To improve the knowledge of matter exchange and pollutant recycling from the sea surface into the atmosphere, a spray drop adsorption model (SDAM) was developed and the validity of the proposed model verified by the following experimental results: (1) an increase of surfactant matter on the sea surface during rough sea conditions (‘surface wave concentration'); (2) an (hyperbolic-like) increase of the enrichment ratio (ER) of surfactant fluorescent organic matter (SFOM), made up predominantly by humic substances (HS), as the particle size decrease; (3) a similar behaviour for elements with pollutant properties, and which are known to interact with HS and other surfactant materials, considered pollution tracers. An additional laboratory experiment, based on the adsorption model conditions, gives enrichment ratio greater than unity for K and Ca. The first results on marine aerosols trapped in marine clouds (at 1000 m above sea level and at 100 km from the coast) seem to further support the proposed model and its ability to predict the transition from saline to almost entirely organic particles for the smaller fractions of marine aerosols. The possible contribution of these particles to the recycling and to the long range transport of pollutants via marine aerosols has been considered.     

Peptide decomposition by extracellular hydrolysis in coastal seawater and salt marsh sediment

Extracellular peptide hydrolysis rates were measured in seawater and sediment from Flax Pond salt marsh using peptide analogs (LYA-peptides) as substrates. This technique allows the direct measurement of specific hydrolysis products and thus provides insights into enzymatic hydrolysis pathways. In sediments, hydrolysis rate constants of LYA-peptides varied seasonally and with depth. Highest activity was found in spring and summer, and most cores exhibited a subsurface maximum. Calculations using the concentrations of chemically-measured peptides suggested that extracellular hydrolysis of peptides is faster than the rate of free amino acids uptake. However, not all peptides may be available for enzymatic hydrolysis. In both seawater and sediment, extracellular hydrolysis of peptides of up to 8 amino acids yielded smaller peptides and free amino acids. Hydrolysis rates depended on size of the peptide substrate, although a clear relationship with number of amino acid constituents was not evident. Peptides containing >2 amino acids were hydrolyzed 10–400 times faster than dipeptides or the fluorogenic substrate Leucine-MCA. Thus, dipeptidases are either uncommon in nature, or hydrolysis is carried out by nonspecific hydrolases that with a low affinity for dipeptides. This is also suggested by the presence of a lag time before dipeptide hydrolysis begins, and the absence of dipeptide hydrolysis in 0.2-μm-filtered. One implication of this finding is that measurements of hydrolysis rates using substrates like Leu-MCA may not accurately predict the magnitude of hydrolysis rates of macromolecules in the marine environment. Even though dipeptide hydrolysis is slow compared to that of larger peptides, LYA-dipeptides are preferentially produced from the hydrolysis of larger substrates. LYA-dipeptides do not penetrate cell membranes of microorganisms because of their size, but natural dipeptides are smaller and can be transported across the cell membrane. Since dipeptides do not appear to accumulate in natural waters, they must be rapidly removed by microorganisms.     

Heavy metals in particulate matter and sediments in the southern Barcelona sedimentation system (North-western Mediterranean)

Concentrations of selected heavy metals (Cr, Cu, Ni, Pb and Zn) from surface sediments, suspended particulate matter and settling particles in the southern Barcelona continental margin were studied in order to evaluate the environmental impact of the anthropogenic metals discharged by the Llobregat River in this Mediterranean area. The temporal variation of heavy metals discharged by this river onto the continental shelf is clearly related to the river water flow. Part of the fine sediment and associated heavy metals transported by the Llobregat River during periods of low river flow accumulate on the river bed, and they are totally removed and discharged onto the Barcelona continental shelf during sporadic river water flow increases. Metals produce significant anomalies of chromium (×2.5), copper (×3.4) and zinc (×3.7) in the surface sediments of the Llobregat prodelta and tend to be transported along the continental shelf following the mean flow. Metals associated with the finest suspended flocs transferred to the slope are controlled by the shelf-slope density front and are transported along slope by the general geostrophic current, instead of accumulating and becoming concentrated in the slope bottom sediments. Settling particulate matter collected in sediment traps on the Barcelona continental slope offshore of the shelf-slope front shows low heavy metal concentrations except in a few sediment trap samples that are significantly metal-enriched in chromium (×4.5) and zinc (×6.8). This enrichment is associated with very short and sporadic river flow increases and is only recorded inside the Foix submarine canyon, which acts as a preferential conduit for the shelf-slope sediment transfer.     

新型城市污泥固化土工程特性及微观机理

通过污泥固化技术可以将城市污泥转化为一种新型城市污泥固化土。为了研究污泥固化土工程特性,对新型城市污泥固化土进行无侧限强度试验、收缩特性试验、浸出毒性试验以及X射线衍射试验与微观结构测试。试验结果表明,城市污泥固化土无侧限抗压强度随期龄增加而增长,28 d后基本稳定;新型城市污泥固化土的线缩率随龄期的增大而增大,且28 d后趋于稳定值;与消化后城市污泥相比,城市污泥固化土中的浸出毒性明显减少,重金属浸出量均符合国家规范要求。消化城市污泥衍射峰中氢氧化钙峰值很高,但随着养护期龄的增长,城市污泥固化土中氢氧化钙的衍射峰值减小,碳酸钙的衍射峰值增大,说明固化土各成分反应越充分,强度越高。微结构测试研究表明,污泥固化土SEM图像中有大量的纤维状物质联结着土颗粒和颗粒团块,形成土骨架纤维的交互空间结构,提高了土体强度。