Cenozoic Climatic Variation Recorded by Quartz and Clay Minerals in North Pacific Sediments

Author(s):  
Cynthia T. Schramm
1972 ◽  
Vol 28 (4) ◽  
pp. 138-144 ◽  
Author(s):  
Saburo Aoki ◽  
Toshio Sudo

2005 ◽  
Vol 176 (2) ◽  
pp. 171-182 ◽  
Author(s):  
Johann Schnyder ◽  
Georges Gorin ◽  
Mohamed Soussi ◽  
François Baudin ◽  
Jean-François Deconinck

Abstract In order to precise the paleogeographic extension of the climatic variation known at the Jurassic/Cretaceous boundary, the sedimentary organic matter (palynofacies and Rock-Eval) and the clay minerals content of Berriasian sediments of the Sidi Kralif Formation are studied on the Jebel Meloussi section, central Tunisia. Standard sedimentological and palynofacies analysis allow to reconstruct the bathymetric curve and the sequence stratigraphic scheme. Using existing biostratigraphy based on calpionellids and ammonite zonation, the sequence stratigraphic interpretation can be correlated with the established eustatic chart. Clay mineral assemblages are characterized by a shift in the kaolinite content, recorded at the end of the calpionellid zone B, at the early/middle Berriasian boundary, at a time of high long-term sea-level (MFS Be2, second order eustatic peak). A contemporary change in the clay mineral assemblages, interpreted as a climatic change, is known from the boreal area, and from the northern margin of the Tethys Sea. That change is also documented southerly in southern Morocco (Agadir area), on the Atlantic domain. A late Tithonian to early Berriasian dry and cooler phase is replaced by a middle to late Berriasian more humid phase, indicated by a general increase in kaolinite in the clay mineral assemblages. The trend from a dry climatic phase to a more humid one, recorded on the boreal domain and along the northern margin of the Tethys is also recorded in lower paleolatitudes of Tunisia, on the southern margin of the Tethys, in better dated outcrops than the ones of Morocco. The results obtained in Tunisia show that the beginning of the climatic change was precisely synchronous on both margins, and occurred within the same long-term high sea-level context.


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.


2019 ◽  
Vol 617-618 ◽  
pp. 221-244 ◽  
Author(s):  
MR Baker ◽  
ME Matta ◽  
M Beaulieu ◽  
N Paris ◽  
S Huber ◽  
...  

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

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