Clay-mineral distribution in recent deep-sea sediments around Taiwan: Implications for sediment dispersal processes

2021 ◽  
pp. 228974
Author(s):  
Kalyani Nayak ◽  
Andrew Tien-Shun Lin ◽  
Kuo-Fang Huang ◽  
Zhifei Liu ◽  
Nathalie Babonneau ◽  
...  
Clay Minerals ◽  
1993 ◽  
Vol 28 (1) ◽  
pp. 61-84 ◽  
Author(s):  
M. Thiry ◽  
T. Jacquin

AbstractThe distribution of clay minerals from the N and S Atlantic Cretaceous deep-sea sediments is related to rifting, sea-floor spreading, sea-level variations and paleoceanography. Four main clay mineral suites were identified: two are inherited and indicative of ocean geodynamics, whereas the others result from transformation and authigenesis and are diagnostic of Cretaceous oceanic depositional environments. Illite and chlorite, together with interstratified illite-smectite and smectite occur above the sea-floor basalts and illustrate the contribution of volcanoclastic materials of basaltic origin to the sediments. Kaolinite, with variable amounts of illite, chlorite, smectite and interstratified minerals, indicates detrital inputs from continents near the platform margins. Kaolinite decreases upward in the series due to open marine environments and basin deepening. It may increase in volume during specific time intervals corresponding to periods of falling sea-level during which overall facies regression and erosion of the surrounding platforms occurred. Smectite is the most abundant clay mineral in the Cretaceous deep-sea sediments. Smectite-rich deposits correlate with periods of relatively low sedimentation rates. As paleoweathering profiles and basal deposits at the bottom of Cretaceous transgressive formations are mostly kaolinitic, smectite cannot have been inherited from the continents. Smectite is therefore believed to have formed in the ocean by transformation and recrystallization of detrital materials during early diagenesis. Because of the slow rate of silicate reactions, transformation of clay minerals requires a long residence time of the particles at the water/sediment interface; this explains the relationships between the observed increases in smectite with long-term sea-level rises that tend to starve the basinal settings of sedimentation. Palygorskite, along with dolomite, is relatively common in the N and S Atlantic Cretaceous sediments. It is not detrital because correlative shelf deposits are devoid of palygorskite. Palygorskite is diagnostic of Mg-rich environments and is indicative of the warm and hypersaline bottom waters of the Cretaceous Atlantic ocean.


2021 ◽  
Vol 9 (11) ◽  
pp. 1254
Author(s):  
Haifeng Wang ◽  
Liang Yi ◽  
Xiguang Deng ◽  
Gaowen He

Global climate and oceanic water masses have undergone profound changes during the middle Pleistocene transition; however, due to a lack of foraminiferal fossils, the nonfossiliferous pelagic deposits were less detected in previous reports. In this work, a gravity core from the Kamehameha Basin in the Central Pacific was studied in terms of magnetostratigraphy, clay mineral and geochemical elements. The main results are: (1) nine magnetozones are recognized in the core, which can be correlated to the geomagnetic polarity timescale from chrons C2n to C1n; (2) smectite is the dominant clay mineral, and the others are illite, chlorite and kaolinite; and (3) the sediments are mainly composed of Al2O3, Fe2O3, MnO, Na2O and TiO2. Based on these results, a geochronological framework for the study area was established, and the depositional rates are estimated as 3–7 m/Myr in the Quaternary, showing an increase during the middle Pleistocene transition. By comparing the findings to various paleoenvironmental processes, it is inferred that the increased sedimentation in the Kamehameha Basin may have resulted from the induced weathering processes and the strengthened aeolian inputs from inner Asia. Moreover, regional circulation related to bottom water evolution has experienced a rapid reorganization across the middle Pleistocene transition. All these findings illustrate the potential of deep-sea sediments in the central tropical Pacific in revealing some key features in paleoclimatology and paleoceanography, which are worthy of further investigation in the future.


Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 196
Author(s):  
Jiangbo Ren ◽  
Yan Liu ◽  
Fenlian Wang ◽  
Gaowen He ◽  
Xiguang Deng ◽  
...  

Deep-sea sediments with high contents of rare-earth elements and yttrium (REY) are expected to serve as a potential resource for REY, which have recently been proved to be mainly contributed by phosphate component. Studies have shown that the carriers of REY in deep-sea sediments include aluminosilicate, Fe-Mn oxyhydroxides, and phosphate components. The ∑REY of the phosphate component is 1–2 orders of magnitude higher than those of the other two carriers, expressed as ∑REY = 0.001 × [Al2O3] − 0.002 × [MnO] + 0.056 × [P2O5] − 32. The sediment P2O5 content of 1.5% explains 89.1% of the total variance of the sediment ∑REY content. According to global data, P has a stronger positive correlation with ∑REY compared with Mn, Fe, Al, etc.; 45.5% of samples have a P2O5 content of less than 0.25%, and ∑REY of not higher than 400 ppm. The ∑REY of the phosphate component reaches n × 104 ppm, much higher than that of marine phosphorites and lower than that of REY-phosphate minerals, which are called REY-rich phosphates in this study. The results of microscopic observation and separation by grain size indicate that the REY-rich phosphate component is mainly composed of bioapatite. When ∑REY > 2000 ppm, the average CaO/P2O5 ratio of the samples is 1.55, indicating that the phosphate composition is between carbonate fluoroapatite and hydroxyfluorapatite. According to a knowledge map of sediment elements, the phosphate component is mainly composed of P, Ca, Sr, REY, Sc, U, and Th, and its chemical composition is relatively stable. The phosphate component has a negative Ce anomaly and positive Y anomaly, and a REY pattern similar to that of marine phosphorites and seawater. After the early diagenesis process (biogeochemistry, adsorption, desorption, transformation, and migration), the REY enrichment in the phosphate component is completed near the seawater/sediment interface. In the process of REY enrichment, the precipitation and enrichment of P is critical. According to current research progress, the REY enrichment is the result of comprehensive factors, including low sedimentation rate, high ∑REY of the bottom seawater, a non-carbonate depositional environment, oxidation conditions, and certain bottom current conditions.


Author(s):  
Dingquan Wang ◽  
Jianxin Wang ◽  
Runying Zeng ◽  
Jie Wu ◽  
Shijia V. Michael ◽  
...  
Keyword(s):  
Deep Sea ◽  

2020 ◽  
Vol 40 ◽  
pp. 101488
Author(s):  
Simone Lechthaler ◽  
Jan Schwarzbauer ◽  
Klaus Reicherter ◽  
Georg Stauch ◽  
Holger Schüttrumpf

Sign in / Sign up

Export Citation Format

Share Document