Authigenic Minerals of Paleozoic–Cenozoic Volcanogenic-Sedimentary Rocks in the Southern Primorye Region

2021 ◽  
Vol 15 (6) ◽  
pp. 583-601
Author(s):  
A. V. Mozherovsky
2021 ◽  
Vol 40 (6) ◽  
pp. 100-110
Author(s):  
A.V. Mozherovsky ◽  

Authigenic minerals in volcanogenic-sedimentary and sedimentary rocks of Southern Primorye from Permian to Miocene time have been studied. Corrensite, rectorite, highly ordered mixed-layer differences of the chlorite-smectite (corrensite-like) and mica-smectite (rectorite-like) types, mica, vermiculite-like differences (?), chlorite, defective chlorite, kaolinite, smectite, calcite, and zeolites were found. Such a set of minerals indicates that the sedimentary layer in the studied sedimentary basins could be three to five kilometer thick, and the temperature of their formation is more than 150°C. The formation of the Lower Cretaceous and Paleocene sedimentary strata has similar features, and probably proceeded first in a shallow sea basin setting of the continental margin (rift stage), sometimes under conditions close to evaporitic (presence of corrensite?), with a frequent change of the facial situation from shallow to deep sedimentation, episodic supplies of volcanic material, and gradual deepening of sedimentation basins. It can be assumed that in Early Cretaceous and Paleogene times, a series of discrete sedimentation basins along the northeastern Asia continental margin developed in a single mineralogical, tectonic, and sedimentological regime of crustal extension: minerals accumulated in the sediments, which in the process of epigenesis transformed in the following directions: a) smectite-rectorite-mica; and b) smectite (palygorskite, sepiolite?) - corrensite-chlorite. In the studied sedimentary complexes three mineralogical «layers» are distinguished: 1) chlorite-mica – mica-chlorite (Permian - Cretaceous); 2) transitional from chlorite and mica to smectite - developed are corrensite, rectorite and highly ordered mixed-layer corrensite-like and rectorite-like minerals (Cretaceous - Paleocene-Eocene), and 3) smectite (from Oligocene to the present).


2008 ◽  
Vol 23 (2) ◽  
pp. 243-273 ◽  
Author(s):  
Trudy Doelman ◽  
Robin Torrence ◽  
Vladimir Popov ◽  
Mihail Ionescu ◽  
Nickolay Kluyev ◽  
...  

1962 ◽  
Vol 99 (1) ◽  
pp. 63-68 ◽  
Author(s):  
Philip F. Hutchins

AbstractPostdepositional low-temperature mineralogical changes in Carboniferous sedimentary rocks from Vestspitsbergen are described. These include the crystallization of apatite, quartz, and feldspar, and the replacement of feldspar and quartz by calcite and dolomite. Minerals of the chalcedonite–lutecime–quartzine group also occur.


2016 ◽  
Vol 22 (1-2) ◽  
Author(s):  
Aleš Novotný ◽  
Renata Čopjaková

Titanite is a common accessory mineral of magmatic rocks, low- and medium-grade metamorphic rocks and it occurs as a detrital mineral in clastic sediments. Our paper deals with titanite alterations as a result of interaction of diagenetic fluids with detrital titanite during deep burial of sedimentary rocks of Drahany Upland, Protivanov Formation. Detrital titanites and their alteration products were examined by electron microprobe. Titanite dissolution was observed from the rim and along the cracks, accompanied by the formation of an authigenic calcite, TiO2 phase, synchysite-(Ce), and rarely chlorite. With an increasing degree of alteration, detrital titanite occurs as small irregular relics inside a mixture of authigenic minerals. Based on the composition of authigenic minerals, we can suppose diagenetic fluid rich in CO2, F and Ca responsible for alteration of detrital titanite. The maximum temperatures in this area during deep burial of sedimentary rocks reached 250–300 °C, corresponding to the conditions of very low-grademetamorphism. Contents of REE (0.67–3.55 wt. % REE2O3) in detrital titanite are rather high and vary significantly. Authigenic synchysite-(Ce) compared with detrital titanite strongly prefers LREE over HREE, indicating that LREE released during dissolution of detrital titanite were preferentially incorporated into the structure of synchysite-(Ce), whereas HREE were mobilized and removed away by diagenetic fluids.


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