Characterization of particle size and settling velocity of cohesive sediments affected by a neutral exopolymer

In natural waters,exopolymers or extracellular polymeric substances(EPS) exuded by microorganisms interact with clay particles,resulting in the flocculation of clays and hence alteration to the properties of suspended cohesive sediments.To investigate and further understand how neutral EPS affect cohesive sediment transport and the final sediment yield,an experimental study was conducted on laboratory-prepared clay and guar gum(used as an analog for neutral EPS) suspensions to characterize EPS-induced flocculation and the settling velocity of resultant floes.Four different clays consisting of kaolinite,illite,Ca-montmorillonite,and Na-montmorillonite were studied to examine the influence of different layer charges on clay flocculation induced by neutral EPS.Floc size was determined by a laser particle size analyzer,and settling velocity estimated by analyzing the time-series floc settling images captured by an optical microscope.Results indicate that neutral EPS promote clay-EPS flocculation for all four clays with the particle/floc size significantly increased from～0.1-60μm to as large as～600μm.Clays’ layer charge has a profound influence on the clay-EPS flocculation.With the same floc size,the settling velocity of clay-EPS flocs is typically smaller than that of pure clay flocs,which is attributed to the reduced density of flocs caused by the EPS. However,for flocs of the same composition(e.g.pure clay or hybrid clay-EPS mixture),the settling velocity increases with size.The fractal dimension of these clay-EPS flocs estimated from settling velocity ranges from 1.39 to 1.47,which are smaller than that of pure clay flocs,indicating that these flocs are less compacted than the pure clay flocs.     

Touhuanping Fault, an active wrench fault within fold-and-thrust belt in northwestern Taiwan, documented by spatial analysis of fluvial terraces

This study aims at the recent activity and development of an active wrench fault, the Touhuanping Fault in northwestern Taiwan. Northwestern Taiwan has been proposed in a current situation between the mature to waning collision in terms of tectonic evolution. The main drainage in this area, the Chungkang River, flows close to the trace of the fault mentioned above. We examined various types of deformation of fluvial terraces along the Chungkang River as a key to understanding the nature and rate of the late Quaternary tectonics. The E–W trending Touhuanping Fault has long been mapped as a geological boundary fault, but its recent activity was suspected. Field survey revealed that its late Quaternary activity is recorded in the offset fluvial terraces. Our result shows dextral slip and vertical offset with upthrown side on the south, and activated at least twice since the emergence of terrace 4 (older terrace 3 with OSL date of ca. 80 ka). Total amount of offset recorded in the Touhuanping terrace sequence is 15 m for dextral and 10 m for vertical offset. Estimated recurrence time of earthquake rupture may be a few tens of thousand years. Uplift on the upthrown side of the Touhuanping Fault also resulted in the formation of drowned valleys which were graded to terrace 4. Other deformation features, such as back-tilting, westward warping, and a range-facing straight scarp, were also identified. A second-order anticline roughly parallel to the Touhuanping Fault is suggested to be the origin of the northward tilting on terrace 3; it could have resulted from a flower structure on the Touhuanping Fault at shallow depth. This may demonstrate that the buried segment of the Touhuanping Fault has also been active since 80 ka. In the northern study area, the westward warping at terrace 2 probably represents late Quaternary activity of another NE–SW trending Hsincheng Fault.     

Aggregation of montmorillonite and organic matter in aqueous media containing artificial seawater

Background  

The dispersion-aggregation behaviors of suspended colloids in rivers and estuaries are affected by the compositions of suspended materials (i.e., clay minerals vs. organic macromolecules) and salinity. Laboratory experiments were conducted to investigate the dispersion and aggregation mechanisms of suspended particles under simulated river and estuarine conditions. The average hydrodynamic diameters of suspended particles (representing degree of aggregation) and zeta potential (representing the electrokinetic properties of suspended colloids and aggregates) were determined for systems containing suspended montmorillonite, humic acid, and/or chitin at the circumneutral pH over a range of salinity (0 – 7.2 psu).     

Polymetallic Mineralization at the Nakakoshi Copper Deposits, Central Hokkaido, Japan

Abstract: Polymetallic mineralization at the Nakakoshi deposits, Kamikawa town, central Hokkaido, occur as fracture-filling veins in Cretaceous slate of the Hidaka Supergroup. Ten veins have been recognized in NE-SW and E-W directions. Sericite in altered slate which is the host of the deposits, was dated at 31. 1 Ma, Oligocene in age.
No. 9 vein consists of massive chalcopyrite ore with various kinds of minerals such as pyrite, pyrrhotite, arsenopyrite, sphalerite, tetrahedrite, Ag-minerals and Cu–Zn–Fe–In–Sn–S minerals, quartz and sericite. Chalcopyrite and pyrite contain sphalerite star and sphalerite with chalcopyrite emulsions. Maximum indium contents of sphalerite and the Cu–Zn–Fe–In–Sn–S minerals are 1. 8 and 16. 3 wt%, respectively. The sulfur isotopic ratios, δ³⁴S of ore minerals, range from –12. 9 to –9. 6%. Formation temperatures of the sulfide minerals are estimated as 300–500°C, based on the paragenesis and chemical compositions of the minerals.     

Heating experiments of the Tagish Lake meteorite: Investigation of the effects of short‐term heating on chondritic organics

We present in this study the effects of short‐term heating on organics in the Tagish Lake meteorite and how the difference in the heating conditions can modify the organic matter (OM) in a way that complicates the interpretation of a parent body's heating extent with common cosmothermometers. The kinetics of short‐term heating and its influence on the organic structure are not well understood, and any study of OM is further complicated by the complex alteration processes of the thermally metamorphosed carbonaceous chondrites—potential analogues of the target asteroid Ryugu of the Hayabusa2 mission—which had experienced posthydration, short‐duration local heating. In an attempt to understand the effects of short‐term heating on chondritic OM, we investigated the change in the OM contents of the experimentally heated Tagish Lake meteorite samples using Raman spectroscopy, scanning transmission X‐ray microscopy utilizing X‐ray absorption near edge structure spectroscopy, and ultraperformance liquid chromatography fluorescence detection and quadrupole time of flight hybrid mass spectrometry. Our experiment suggests that graphitization of OM did not take place despite the samples being heated to 900 °C for 96 h, as the OM maturity trend was influenced by the heating conditions, kinetics, and the nature of the OM precursor, such as the presence of abundant oxygenated moieties. Although both the intensity of the 1s?σ* exciton cannot be used to accurately interpret the peak metamorphic temperature of the experimentally heated Tagish Lake sample, the Raman graphite band widths of the heated products significantly differ from that of chondritic OM modified by long‐term internal heating.     

Further characterization of carbonaceous materials in Hayabusa‐returned samples to understand their origin

Carbonaceous materials in the sample catcher of the Hayabusa spacecraft were assigned as category 3 particles. We investigated the category 3 particles with a suite of in situ microanalytical methods. Possible contaminants collected from the cleanrooms of the spacecraft assembly and extraterrestrial sample curation center (ESCuC) were also analyzed in the same manner as category 3 particles for comparison. Our data were integrated with those of the preliminary examination team for category 3 particles. Possible origins for the category 3 particles include contamination before and after the operation of the Hayabusa spacecraft.     

Soil column experiments for iodate and iodide using K-edge XANES and HPLC–ICP-MS

Radioactive iodine is one of the most problematic radionuclides because of its long half life and high mobility. Mobility of iodine depends on the chemical form to a great extent. This paper reports the results of soil column experiments we conducted to evaluate the mobilities of IO₃⁻ and I⁻. In order to determine the mechanisms of adsorption of IO₃⁻ and I⁻ on soil, adsorption isotherms were obtained by batch experiments. Both adsorption isotherms of IO₃⁻ and I⁻ are well explained by Langmuir model. The adsorption maximum of IO₃⁻ is about five times larger than that of I⁻. In the column experiments, iodine distributions between soil and pore water in the soil column were determined at various depths. Chemical forms of iodine in soil and pore water were determined by X-ray absorption near-edge structure (XANES), and high performance liquid chromatography connected to inductively coupled plasma mass spectrometry (HPLC–ICP-MS), respectively. Vertical profiles of iodine in pore water were simulated using Visual MODFLOW. Our results showed, upon I⁻ infiltration through the column, that a small amount of I⁻ adsorbed on soil, and its mobility is mainly controlled by advection and dispersion. The profile of iodine concentration in pore water was well simulated by assuming equilibrium-controlled Langmuir type adsorption without considering any chemical transformations. For the IO₃⁻ addition system into the column, however, IO₃⁻ adsorbed to soil to a larger degree, which causes a much larger retardation effect than I⁻. In addition, reduction of IO₃⁻ to I⁻ was also confirmed in both soil and pore water by XANES and HPLC–ICP-MS, respectively. The fraction of I⁻ increased toward the deeper end in both phases because of its lower affinity for soil than IO₃⁻, where the reduced I⁻ was released to the pore water and transported by the water flow. In this study, such reduction effect was clearly demonstrated by the speciation analyses of iodine in both soil and water phases, which confirmed that the mobility of I⁻ is a dominant factor that controls the fate of iodine in the surface environment.     

Alteration of ferrihydrite reductive dissolution and transformation by adsorbed As and structural Al: Implications for As retention

Reduction of As(V) and reductive dissolution and transformation of Fe (hydr)oxides are two dominant processes controlling As retention in soils and sediments. When developed within soils and sediments, Fe (hydr)oxides typically contain various impurities—Al being one of the most prominent—but little is known about how structural Al within Fe (hydr)oxides alters its biotransformation and subsequent As retention. Using a combination of batch and advective flow column studies with Fe(II) and Shewanella sp. ANA-3, we examined (1) the extent to which structural Al influences reductive dissolution and transformations of ferrihydrite, a highly reactive Fe hydroxide, and (2) the impact of adsorbed As on dissolution and transformation of (Al-substituted) ferrihydrite and subsequent As retention. Structural Al diminishes the extent of ferrihydrite reductive transformation; nearly three-orders of magnitude greater concentration of Fe(II) is required to induce Al-ferrihydrite transformation compared to pure two-line ferrihydrite. Structural Al decreases Fe(II) retention/incorporation on/into ferrihydrite and impedes Fe(II)-catalyzed transformation of ferrihydrite. Moreover, owing to cessation of Fe(II)-induced transformation to secondary products, Al-ferrihydrite dissolves (incongruently) to a greater extent compared to pure ferrihydrite during reaction with Shewanella sp. ANA-3. Additionally, adsorption of As(V) to Al-ferrihydrite completely arrests Fe(II)-catalyzed transformation of ferrihydrite, and it diminishes the difference in the rate and extent of ferrihydrite and Al-ferrihydrite reduction by Shewanella sp. ANA-3. Our study further shows that reductive dissolution of Al-ferrihydrite results in enrichment of Al sites, and As(V) reduction accelerates As release due to the low affinity of As(III) on these non-ferric sites.     

Compositional diversity in insoluble organic matter in type 1, 2 and 3 chondrites as detected by infrared spectroscopy

Insoluble organic matter (IOM) isolated from 22 carbonaceous and ordinary chondrites spanning a wide range of groups and petrologic types were analyzed using Fourier transform infrared spectroscopy (FTIR). Based on common IR spectral features, it is observed that IOM falls into 4 molecularly distinct groups (designated here as A through D). Spectral group A includes type 1 and 2 chondrites and exhibits intense aliphatic C-H and carboxyl vibrational peaks. Spectral group B includes the least metamorphosed type 3 chondrites and Tagish Lake, and exhibits weaker aliphatic and carboxyl vibrational intensity. Spectral groups C and D include metamorphosed type ?3.1 chondrites and a heated CM chondrite. The carbonyl stretching features in spectral groups C and D differ from that in spectral groups A and B and from each other. In spectral group C, the carbonyl stretching is assigned to cyclic unsaturated lactones; in spectral group D carbonyl exists predominantly in the form of unsaturated ketone moieties. Both spectral groups C and D have a relatively narrow band structure around 1210 cm⁻¹ (assigned to aromatic skeletal modes) as compared with spectral groups A and B, which is consistent with the formation of more condensed aromatics by extensive thermal metamorphism. The differences in carbonyl structures in spectral groups C and D are not the result of different effective metamorphic temperatures, rather these differences likely result from variation in the activity of water and oxygen at different stages of parent body metamorphism. Such environmental variations must be local phenomena in the parent bodies as there is no correlation between spectral grouping and chondrite class or group.