Whole-rock Geochemistry of Basic Schists from the Besshi Area, Central Shikoku: Implications for the Tectonic Setting of the Besshi Sulfide Deposit

Abstract. Whole-rock chemical compositions of the Besshi basic schist closely associated with the Besshi massive sulfide deposit from the Sanbagawa Belt are reported. Studied samples were collected from four outcrops around the Dozan-goe, central Shikoku. Common metamorphic mineral assemblage of the basic schist is albite + epidote + actinolite + chlorite ± muscovite ± quartz. Major element contents are similar to those of typical tholeiitic basalts. Trace element patterns of the basic schist normalized to normal mid-ocean ridge basalt (N-MORB) are generally flat, although concentrations of highly mobile large-ion lithophile elements are quite variable. Chondrite-normalized rare earth element (REE) patterns are flat to slightly light REE-depleted patterns. In the Hf-Th-Ta and Nb-Zr-Y discrimination diagrams, basic schist samples closely associated with the sulfide deposit are plotted within the N-MORB field. The Th/Nb ratios of the basic schist are also comparable to those of N-MORB. These geo-chemical lines of evidence indicate that the protolith of the Besshi basic schist is N-MORB and the Besshi sulfide deposit was formed by hydrothermal activity in conjunction with MOR volcanism.     

Precise Determination of Ultra-Low (sub-ng g-1) Level Rare Earth Elements in Ultramafic Rocks by Quadrupole ICP-MS

We present a new method that determines precisely and accurately rare earth elements (REE) at the sub-ng g^-1 level in ultramafic rocks based on acid dissolution and quadrupole ICP-MS with systematic interference corrections on each sample. The method is demonstrated by analyses of the international geochemical reference materials, PCC-1 (peridotite), DTS-1 (dunite) and DTS-2 (dunite) provided by the United States Geological Survey (USGS), and JP-1 (peridotite) issued by the Geological Survey of Japan (GSJ). Detection limits, as rock equivalent, were calculated to be 0.01-0.08 ng g^-1 for our instrument, which is sufficiently low compared to the REE concentrations of ultramafic rocks. In addition, procedural blanks of the proposed method were 0.2-5 pg, which is negligible even for the ultra-low level REE determinations. Reproducibility obtained from separate dissolutions and measurements of USGS DTS-2 and GSJ JP-1 was 3-6%, which corresponds to the high-precision data obtained by ID-TIMS or magnetic sector field ICP-MS with a desolvating nebuliser. The REE data determined exhibit smooth chondrite-normalised REE patterns for all of the tested geochemical reference materials, and the abundances are in good agreement with recently published data.     

Influence of Surface-Based Stable Layer Development on Asian Dust Behaviour Over Tokyo

The relationship between local meteorological fields and the behaviour of airborne Asian dust that arrived in the Tokyo metropolitan area on 1 April 2007 with the passage of a synoptic-scale cold front has been investigated through Doppler lidar observations, experiments using a regional atmospheric numerical model, and analyses of surface and upper-air meteorological observations. Results of the Doppler lidar observations showed that the Asian dust passed above the metropolitan area with strong south-westerly winds with speeds of 15–26 m s⁻¹. Meteorological fields reproduced by the numerical experiments showed the development of a surface-based stable layer in the metropolitan area caused by nocturnal radiational cooling near the ground surface and south-westerly warm air advection at upper levels. The blocking effect of the mountainous region located to the west of the metropolitan area induced an area of stagnant air inside the metropolitan area and promoted the stable layer development. Although strong downdrafts prevailed in the upper air, the airborne Asian dust did not spread to the ground when the stable layer was formed. These results strongly indicate that the developed stable layer prevented strong downdrafts from spreading to the ground, acting as an obstacle to the transport of the Asian dust particles from the upper air towards the ground. This is considered to be one of the main causes of the low appearance frequency of Asian dust phenomena near the ground in the Tokyo metropolitan area and eastern Japan.     

A Simple Method for Precise Determination of 23 Trace Elements in Granitic Rocks by ICP-MS after Lithium Tetraborate Fusion

Abstract. An improved alkali fusion method followed by HF-HNO₃-HC1O₄ treatment is performed for simultaneous determination of 23 trace elements (Sr, Y, Zr, Nb, Ba, Hf, Ta, Th, U, and REE) by ICP-MS in rock reference materials: basaltic rocks (JB-2, JB-3) and granitic rocks (JG-la, JG-2, JG-3). Our improved method offers several advantages including: (1) suppression of whitish precipitates probably composed of insoluble fluorides by addition of HCIO4, (2) simple and reliable preparation procedure, (3) instrument calibration which enables straightforward simultaneous multi-elemental analysis, and (4) the very low background levels by using pure lithium tetraborate flux. We obtained the analytical results with a reproducibility of mostly <2 % (1) for the basaltic rocks and <7 % for the granitic rocks. The higher relative standard deviation (RSD) values for granitic rocks may be attributed to sample heterogeneity of coarse-grained granitic rocks. The analytical results of the granitic rocks demonstrate that Zr and Hf abundances are consistent with the compiled values and that REE concentrations agree well with recently published data, suggesting that the Li₂B₄O₇ fusion method applied in the present study is suitable for the analysis of the granitic rocks.     

Carbonatization of oceanic crust by the seafloor hydrothermal activity and its significance as a CO2 sink in the Early Archean

Early Archean (3.46 Ga) hydrothermally altered basaltic rocks exposed near Marble Bar, eastern Pilbara Craton, have been studied in order to reveal geological and geochemical natures of seafloor hydrothermal carbonatization and to estimate the CO₂ flux sunk into the altered oceanic crust by the carbonatization. The basaltic rocks are divided into basalt and dolerite, and the basalt is further subdivided into type I, having original igneous rock textures, and type II, lacking these textures due to strong hydrothermal alteration. Primary clinopyroxene phenocrysts are preserved in some part of the dolerite samples, and the alteration mineral assemblage of dolerite (chlorite + epidote + albite + quartz ± actinolite) indicates that the alteration condition was typical greenschist facies. In other samples, all primary minerals were completely replaced by secondary minerals, and the alteration mineral assemblage of the type I and type II basalts (chlorite + K-mica + quartz + carbonate minerals ± albite) is characterized by the presence of K-mica and carbonate minerals and the absence of Ca-Al silicate minerals such as epidote and actinolite, suggesting the alteration condition of high CO₂ fugacity. The difference of the alteration mineral assemblages between basalt and dolerite is probably attributed to the difference of water/rock ratio that, in turn, depends on their porosity.Carbonate minerals in the carbonatized basalt include calcite, ankerite, and siderite, but calcite is quite dominant. The δ¹³C values of the carbonate minerals are −0.3 ± 1.2‰ and mostly within the range of marine carbonate, indicating that the carbonate minerals were formed by seafloor hydrothermal alteration and that carbonate carbon in the altered basalt was derived from seawater. Whole-rock chemical composition of the basaltic rocks is essentially similar to that of modern mid-ocean ridge basalt (MORB) except for highly mobile elements such as K₂O, Rb, Sr, and Ba. Compared to the least altered dolerite, all altered basalt samples are enriched in K₂O, Rb, and Ba, and are depleted in Na₂O, reflecting the presence of K-mica replacing primary plagioclase. In addition, noticeable CO₂ enrichment is recognized in the basalt due to the ubiquitous presence of carbonate minerals, but there was essentially neither gain nor loss of CaO. This suggests that the CO₂ in the hydrothermal fluid (seawater) was trapped by using Ca originally contained in the basalt. The CaO/CO₂ ratios of the basalt are generally the same as that of pure calcite, indicating that Ca in the basalt was almost completely converted to calcite during the carbonatization, although Mg and Fe were mainly redistributed into noncarbonate minerals such as chlorite.The carbon flux into the Early Archean oceanic crust by the seafloor hydrothermal carbonatization is estimated to be 3.8 × 10¹³ mol/yr, based on the average carbon content of altered oceanic crust of 1.4 × 10^-3 mol/g, the alteration depth of 500 m, and the spreading rate of 1.8 × 10¹¹ cm²/yr. This flux is equivalent to or greater than the present-day total carbon flux. It is most likely that the seafloor hydrothermal carbonatization played an important role as a sink of atmospheric and oceanic CO₂ in the Early Archean.     

Geochemical Features and Tectonic Setting of Greenstones from Kunimiyama, Northern Chichibu Belt, Central Shikoku, Japan

Abstract. We report whole‐rock chemical data for the greenstones from the Kunimiyama area in the Northern Chichibu Belt and their implications on the tectonic setting of these rocks. The Kunimiyama greenstones are associated with stratiform fer‐romanganese deposits or bedded cherts in the northern part of the study area, but are closely associated with a thick limestone block or bedded cherts in the southern part. The constituent minerals of greenstones are albitized plagioclase, clinopy‐roxene, chlorite, calcite, epidote, pumpellyite, prehnite, quartz, celadonite, sericite and opaque minerals such as iron oxyhy‐droxide and hematite. These mineral assemblages, epidote + pumpellyite + chlorite and chlorite + pumpellyite + prehnite, suggest that the metamorphic grade of greenstones from the Kunimiyama area is prehnite‐pumpellyite facies. The whole‐rock chemical compositions of greenstones associated with ferromanganese deposits are generally similar to those of normal mid‐ocean ridge basalt (N‐MORB). In contrast, the chemical compositions of the greenstones associated with the limestone block are comparable to those of ocean island alkaline basalt. Greenstones associated with bedded cherts are of enriched MORB and ocean island basalt, as well as N‐MORB origins, suggesting they probably formed as a result of plume‐related MOR volcanism in the Panthalassa Ocean in Early Permian and by tectonic mixing of ocean island basalts with oceanic ridge crustal fragments during accretion/subduction processes. These geological and geochemical lines of evidence suggest that the Kunimiyama greenstones are allochthonous blocks of accreted oceanic crust and seamounts. The ferromanganese deposits are frequently accompanied by reddish greenstones. Compared to common greenish greenstones, the reddish greenstones are characterized by high MnO and rare earth element contents and distinct negative Ce anomalies, implying a slight contribution of hydro thermal component forming the ferromanganese deposits.     

Alkalinization and acidification of stream water with changes in atmospheric deposition in a tropical dry evergreen forest of northeastern Thailand

Field surveys on atmospheric deposition and stream water chemistry were conducted in an evergreen forest in northeastern Thailand characterized by a tropical savanna climate with distinct dry and wet seasons. Atmospheric deposition of ion constituents by throughfall and stemflow was shown to increase in the beginning and end of the wet season, reflecting the precipitation pattern. The pH and electrical conductivity of stream water increased with alkalinity and base cation concentrations due to mineralization of organic matter by the first rain and retention of anions in soil during the start of the wet season. After initial alkalinization, the pH and alkalinity declined rapidly with the highest SO₄^2? concentration displayed in the middle towards the end of the wet season. The magnitude of peaks in SO₄^2? concentration (13.5–60.6 μmol_c/L) reflects deposition during the first 2 months of the wet season (March and April) in respective years (60.8–170 mol_c/ha). Release of SO₄^2? with H⁺, which is retained in soil during the early wet season, may cause acidification later in the season. The deposition and concentration of SO₄^2? declined over 6 years. However, the pH of stream water declined with increasing concentrations of SO₄^2? and other major ions. The release of materials accumulated in the ecosystem was facilitated by the decrease in SO₄^2? concentration/deposition and increased precipitation in the middle–late wet season. The retention‐release cycle of SO₄^2? largely contributed to both seasonal and interannual variations in stream water chemistry in the tropical savanna climate studied.     

Stability of a circular tunnel in cohesive-frictional soil subjected to surcharge loading

The stability of circular tunnels in cohesive-frictional soils subjected to surcharge loading has been investigated theoretically and numerically assuming plane strain conditions. Despite the importance of this problem, previous research on the subject is very limited. At present, no generally accepted design or analysis method is available to evaluate the stability of tunnels/openings in cohesive-frictional soils. In this study, continuous loading is applied to the ground surface, and both smooth and rough interface conditions are modelled. For a series of tunnel diameter-to-depth ratios and material properties, rigorous lower- and upper-bound solutions for the ultimate surcharge loading are obtained by applying finite element limit analysis techniques. For practical use, the results are presented in the form of dimensionless stability charts with the actual tunnel stability numbers being closely bracketed from above and below. As an additional check on the solutions, upper-bound rigid-block mechanisms have been developed and the predicted collapse loads from these are compared with those from finite element limit analysis. Finally, an expression that approximates the ultimate surcharge load has been devised which is convenient for use by practising engineers.     

Impact crater formed on sintered snow surface simulating porous icy bodies

To improve the scaling parameter controlling the impact crater formation in the strength regime, we conducted impact experiments on sintered snow targets with the dynamic strength continuously changed from 20 to 200 kPa, and the largest crater size formed on small icy satellites was considered by using the revised scaling parameter. Ice and snow projectiles were impacted on a snow surface with 36% porosity at an impact velocity from 31 m s⁻¹ to 150 m s⁻¹. The snow target was sintered at the temperature from −5 °C to −18 °C, and the snow dynamic strength was changed with the sintering duration at each temperature. We found that the mass ejected from the crater normalized by the projectile mass, π_V, was related to the ratio of the dynamic strength to the impact pressure, , as follows: , where the impact pressure was indicated by P = ρ_tC_0tv_i/2 with the target density of ρ_t, when the impact velocity, v_i, was much smaller than the bulk sound velocity C_0t (typically 1.8 km s⁻¹ in our targets). The ratio of the largest crater diameter to the diameter of the target body, d_max/D, was estimated by calculating the crater diameter at the impact condition for catastrophic disruption and then compared to the observed d_max/D of jovian and saturnian small satellites, in order to discuss the formation condition of these large d_max/D in the strength regime.