Distribution and Accumulation of Clastic and Clay Minerals in Deposits of Various Facies Types

1967 ◽  
pp. 293-349
Author(s):  
N. M. Strakhov ◽  
S. I. Tomkeieff ◽  
J. E. Hemingway
Keyword(s):  
Minerals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 462
Author(s):  
Marcin Krajewski ◽  
Piotr Olchowy

This paper describes and analyzes the Upper Jurassic (Lower Kimmeridgian) succession exposed in the Zakrzówek Horst, located in the Kraków area. Three distinguished facies types FT 1-FT 3 comprise several limestone varieties: sponge-microbial, pelitic-bioclastic, and partly dolomitized detrital-bioclastic. Their sedimentary environments varied from relatively deeper, attaining storm-wave base, to more shallower, probably close to normal-wave base. Characteristic features of limestones are changes in contents of CaCO3 and insoluble residuum as well as porosity values in vertical transitional zones between facies types. The investigated facies types differ in sediment porosity dependent on development of limestones and its susceptibility to mechanical compaction during the early diagenesis. The studied limestones show high CaCO3 contents and minor insoluble residuum contents comprising quartz, chalcedony and clay minerals. No distinct variability occurs in contents of magnesium, silica, alumina and iron accumulated in clay minerals, iron oxides and oxyhydroxides, as well as in the amounts of amorphous silica. Early diagenetic dolomites, which occur locally within the limestones, were unrelated to fracture systems as possible pathways responsible for transfer of solutions rich in Mg2+ ions. The possible source of Mg2+ ions might have been the pore solutions, which migrated from compacted basinal bedded facies towards reef facies or the grain-supported bedded facies developed in the adjacent areas. Microscopic studies revealed dedolomitization at the surfaces and in the inner parts of dolomite crystals. In many cases, dolomite crystals were replaced by calcite forming pseudomorphs.


Author(s):  
N. Kohyama ◽  
K. Fukushima ◽  
A. Fukami

Since the interlayer or adsorbed water of some clay minerals are quite easily dehydrated in dried air, in vacuum, or at moderate temperatures even in the atmosphere, the hydrated forms have not been observed by a conventional electron microscope(TEM). Recently, specific specimen chambers, “environmental cells(E.C.),” have been developed and confirmed to be effective for electron microscopic observation of wet specimen without dehydration. we observed hydrated forms of some clay minerals and their morphological changes by dehydration using a TEM equipped with an E.C..The E.C., equipped with a single hole copper-microgrid sealed by thin carbon-film, attaches to a TEM(JEM 7A) with an accelerating voltage 100KV and both gas pressure (from 760 Torr to vacuum) and relative humidity can be controlled. The samples collected from various localities in Japan were; tubular halloysite (l0Å) from Gumma Prefecture, sperical halloysite (l0Å) from Tochigi Pref., and intermediate halloysite containing both tubular and spherical types from Fukushima Pref..


Author(s):  
J. Thieme ◽  
J. Niemeyer ◽  
P. Guttman

In soil science the fraction of colloids in soils is understood as particles with diameters smaller than 2μm. Clay minerals, aquoxides of iron and manganese, humic substances, and other polymeric materials are found in this fraction. The spatial arrangement (microstructure) is controlled by the substantial structure of the colloids, by the chemical composition of the soil solution, and by thesoil biota. This microstructure determines among other things the diffusive mass flow within the soils and as a result the availability of substances for chemical and microbiological reactions. The turnover of nutrients, the adsorption of toxicants and the weathering of soil clay minerals are examples of these surface mediated reactions. Due to their high specific surface area, the soil colloids are the most reactive species in this respect. Under the chemical conditions in soils, these minerals are associated in larger aggregates. The accessibility of reactive sites for these reactions on the surface of the colloids is reduced by this aggregation. To determine the turnover rates of chemicals within these aggregates it is highly desirable to visualize directly these aggregation phenomena.


2018 ◽  
Vol 52 (4) ◽  
pp. 317-333 ◽  
Author(s):  
Jaeguk Jo ◽  
Toshiro Yamanaka ◽  
Tomoki Kashimura ◽  
Yusuke Okunishi ◽  
Yoshihiro Kuwahara ◽  
...  

2010 ◽  
Vol 30 (4) ◽  
pp. 57-66 ◽  
Author(s):  
Qian GE ◽  
Fengyou CHU ◽  
Jingpu LIU ◽  
Yuansheng DU ◽  
Zuo XUE ◽  
...  

2011 ◽  
Vol 31 (3) ◽  
pp. 11-16 ◽  
Author(s):  
Xianhong LAN ◽  
Xianjun ZHANG ◽  
Xinbo LIU ◽  
Rihui LI ◽  
Zhixun ZHANG

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