The molecular composition of ambers     

J.O. Grimalt  B.R.T. Simoneit  P.G. Hatcher  A. Nissenbaum 《Organic Geochemistry》1988,13(4-6)

Bulk (elemental composition, IR, CP/MAS ¹³C NMR) and molecular (GC-MS) analyses have been performed on a series of ambers and resins derived from different locations (Dominican Republic, Philippines, Canada, Israel, New Zealand, Chile) having diverse botanical affinities (Araucariaceae, Hymenaea) and variable age (from Holocene to Early Cretaceous). No major differences have been observed from the elemental composition and the spectroscopic data; however, the molecular analyses of the solvent extractable fraction show that a specific mixture of components is present in each sample. These are mainly diterpenoid products that in general are also found abundantly in the higher plants from which the ambers and resins originate. Nevertheless, a direct relationship between major terpenoid constituents in fossil resins and precursor plant materials can only be established for the younger samples.Irrespective of the geographical or botanical origin of the ambers and resins, several common age-dependent molecular transformation trends can be recognized: (1) progressive loss of olefinic bonds (especially those located in exocyclic positions), (2) decrease of functionalized products, and (3) increasing proportion of aromatized components. However, even in the samples of older age (Cretaceous) the degree of aromatization is very low when compared with that of other higher-plant related materials such as fossilized woods or low rank coals. This indicates that maturation must involve essentially olefin polymerization processes instead of extensive aromatization.  相似文献   

Tafoni on coastal slopes,South Devon,U.K.     

Derek N. Mottershead  Kenneth Pye 《地球表面变化过程与地形》1994,19(6):543-563

Cavernous weathering (tafoni development) occurs on coastal slopes in greenschist bedrock at elevations up to 40 m above sea level. The freshly weathered surfaces of the cavern interiors are irregular in morphology, discordant to major rock structure, formed by substantially weakened rock and associated with granular weathering debris. The weathering debris contains soluble elements in proportions similar to those present in seawater, and the penetration of elements associated with sea salts into the weathering surface to estimated depths of at least 0·1–0·2 m is indicated by the presence of chlorine. Scanning electron microscopy and microprobe analyses suggest that rock breakdown occurs principally through limited chemical weathering at grain boundaries. The mechanism for the emplacement of marine salts within sheltered rock surfaces in the tafoni is postulated to be a combination of dry deposition under turbulent atmospheric conditions and wetting by coastal fog.  相似文献   

辽宁海洋综合经济区划分的初步探讨   总被引：4，自引：0，他引：4  

张耀光 《地理学报》1994,49(2):139-148

我国是海洋大国，有相当陆域国土面积三分之一的海洋国土。随着海洋资源的开发利用，海洋经济不断发展，海洋经济区逐渐形成。在全国划分经济区时，不应忽视海洋经济区。沿海省区在划分经济区时，更应把海洋列入到省级经济区内。辽宁是我国沿海省区之一，通过对辽宁海洋经济区划分的研究，探讨海洋经济区及其划分的有关理论、实践与方法。  相似文献   

Amino acid nitrogen in atmospheric aerosols: Occurrence,sources and photochemical modification   总被引：2，自引：0，他引：2  

Peter J. Milne  Rod G. Zika 《Journal of Atmospheric Chemistry》1993,16(4):361-398

The presence of amino acids in atmospheric precipitation and aerosols has been noted for many years, yet relatively little is known about these or other nitrogen containing organic compounds in the atmosphere. Marine and continental rainwater analyses indicate that atmospheric aerosols, and subsequently atmospheric precipitation, may contain substantial levels of free and combined amino acids. The most likely source of amino N in the remote marine atmosphere appears to be the injection of proteinaceous material through the action of bursting bubbles at the sea-air interface or the long range transport from terrestrial sources. The capacity of these substrates to undergo photooxidation and photodegradation in the atmosphere to simpler species, such as ammonium ions, carboxylic acids, and for the S containing amino acids, oxidized forms of sulfur, has received little attention from atmospheric chemists. The photochemistry of covalently bound amino groups, particularly as found in peptides and amino acids, is discussed here with the purpose of summarizing what is known of their occurrence and their possible importance to atmospheric chemistry.  相似文献   

Numerical study of the oxidation process of dimethylsulfide in the marine atmosphere   总被引：1，自引：0，他引：1  

Seizi Koga  Hiroshi Tanaka 《Journal of Atmospheric Chemistry》1993,17(3):201-228

A box model, involving simple heterogeneous reaction processes associated with the production of non-sea-salt sulfate (nss-SO ₄ ^2– ) particles, is used to investigate the oxidation processes of dimethylsulfide (DMS or CH₃SCH₃) in the marine atmosphere. The model is applied to chemical reactions in the atmospheric surface mixing layer, at intervals of 15 degrees latitude between 60° N and 60° S. Given that the addition reaction of the hydroxyl radical (OH) to the sulfur atom in the DMS molecule is faster at lower temperature than at higher temperature and that it is the predominant pathway for the production of methanesulfonic acid (MSA or CH₃SO₃H), the results can well explain both the increasing tendency of the molar ratio of MSA to nss-SO ₄ ^2– toward higher latitudes and the uniform distribution with latitude of sulfur dioxide (SO₂). The predicted production rate of MSA increases with increasing latitude due to the elevated rate constant of the addition reaction at lower temperature. Since latitudinal distributions of OH concentration and DMS reaction rate with OH are opposite, a uniform production rate of SO₂ is realized over the globe. The primary sink of DMS in unpolluted air is caused by the reaction with OH. Reaction of DMS with the nitrate radical (NO₃) also reduces DMS concentration but it is less important compared with that of OH. Concentrations of SO₂, MSA, and nss-SO ₄ ^2– are almost independent of NO _x concentration and radiation field. If dimethylsulfoxide (DMSO or CH₃S(O)CH₃) is produced by the addition reaction and further converted to sulfuric acid (H₂SO₄) in an aqueous solution of cloud droplets, the oxidation process of DMSO might be important for the production of aerosol particles containing nss-SO ₄ ^2– at high latitudes.  相似文献   

东亚和西太平洋爆发性温带气旋发生的气候学研究   总被引：3，自引：1，他引：3       下载免费PDF全文

仪清菊  丁一汇 《大气科学》1993,17(3):302-309

本文利用历史天气图资料,对1973—1988年中国东部和沿海地区的温带气旋及其爆发性发展情况进行了统计,共有1014个温带气旋发生,其中有1/5达到了爆发性发展的强度,构成了西太平洋爆发性海洋气旋的一部分.它占整个西太平洋爆发性气旋总频数(包括不同来源)的51％.进而对这类爆发性气旋的活动规律进行了分析,概括出了它们的气候学特征.比较亚洲大陆、中国近海及西太平洋地区的爆发性温带气旋表明,西太平洋地区不仅频繁而且强烈.而东、西太平洋地区发生海洋爆发性气旋的对比表明,二者存在着明显的差异.同时也指出,东太平洋地区爆发性气旋的发生并不是一种少见的现象.  相似文献   

云南金顶铅锌矿床碎屑岩地层中铅锌活化迁移的实验研究   总被引：2，自引：0，他引：2  

姚志健  唐宏 《地球科学》1991,16(2):181-188

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Carboxylic monoacids in the air of mayombe forest (Congo): Role of the forest as a source or sink     

Jean Servant  Georges Kouadio  Bernard Cros  Robert Delmas 《Journal of Atmospheric Chemistry》1991,12(4):367-380

In the tropical rain forests of the Congo during the dry season, from June to September 1987, carboxylic acid partial pressures (P _gas) in the air above the canopy, at ground level, and at the boundary layer, were estimated from water samples such as fog and rainwater. The concentrations of these acids were also measured in the sap of tree leaves. Tree leaves act as a sink or as a source if the acid P _gas is greater of lower than the acid concentrations in molecular form in sap. For each of these soluble gases, there is a value of P _gas where the exchange is nul. This is called the compensation point. Values of the compensation point for some tree leaves were evaluated according to Henry's law. Henry's law coefficients at ppm levels were redetermined for formic (HCOOH), acetic (CH₃COOH), propionic (CH₃CH₂COOH), and isobutyric (CH₃CH(CH₃)COOH) acids.By comparison of P _gas and compensation points, it is concluded that the forest was a potential source for these acids. The soil-or the litter-acts as a significant source of a carboxylic acid of C₃ or C₄ atoms in the aliphatic chain. This carboxylic acid, not yet fully characterized, could play an important role in the rain acidity in forested zones of the equatorial areas.The direct emission of these carboxylic acids by vegetation was the main source in the boundary layer above the forest. The average emissions were 3.1×10⁹, 7.8×10⁹, and 8.4×10⁹ molecules cm^-2 s^-1 for HCOOH, CH₃COOH, and CH₃CH₂COOH, respectively. The savanna is an exogenous source of HCOOH and CH₃CH₂COOH during moderately rainy days for 30% of the time. The ozonolysis of isoprene seems to be a small source of HCOOH.  相似文献   

Organic geochemical studies of a recent Inner Great Barrier Reef sediment—I. Assessment of input sources     

Philip M. Shaw  R.B. Johns 《Organic Geochemistry》1985,8(2):147-156

The concentration of solvent-extractable (SE) and bound hydrocarbons, ketones, alcohols, sterols, monocarboxylic acids, hydroxyacids and α,ω-dicarboxylic acids of a surface sample (0–2.5 cm) from a recent carbonate tropical sediment taken at 60ft (18m) depth north-west of the Low Isles, North Queensland, are reported in detail. n-Alkanes are a minor constituent in the SE and bound hydrocarbon fractions with the major component being unresolved complex hydrocarbon material which is not an anthropogenic input. 6,10,14-Trimethylpentadecan-2-one derived from chlorophyll, as well as phytol, were identified as major components of the ketone and alcohol constituents. No chlorophyll pigments or pigmented degradation products were present, implying degradation before incorporation into the sediment. This conclusion is consistent with evidence for higher-plant input in which all sensitive lipids have been degraded before incorporation. SE and bound fractions have been studied in detail and show considerable differences probably arising from the importance of viable biomass in the SE fraction. Inputs to the sediment are determined as higher plants, algae, bacteria, fungi and meiofauna in descending order of importance.  相似文献   

Simulation of pebble abrasion on coastal benches by transgressive waves     

Gordon E. Bigelow 《地球表面变化过程与地形》1984,9(4):383-390

Tumbler simulations of abrasion processes affecting rocks on basaltic marine benches have clarified the effects of mass and volume of rock fragments on their rate of wear. Several experiments indicate that rate of basalt wear increases with mass in the interval 1 g to 8 g, but is not related to volume of fragments abraded in seawater. Relatively small quantities of rock flour suspended in the immersant seawater substantially reduced the rate of basalt wear. Basalt and calcareous beachrock responded differently in systems with both rock types tumbling together. Examination of the cuttings from these low-energy encounters suggests that abrasion on elevated benches along exposed seacoasts reduces virtually all clastic material to particles of silt size or smaller, producing essentially no sand.  相似文献