Numerical experiments on wind-driven circulations and associated transport processes in Suruga Bay

The dynamics of the wind-driven circulations and surface transport processes in Suruga Bay have been examined by performing numerical experiments. While strong winds exist outside the bay, the winds inside the bays are greatly reduced, which generates a strong wind stress curl in winter and autumn. In particular, in winter, a strong positive curl region is located across the bay mouth, and a strong surface circulation with counterclockwise rotation is generated beneath it. The circulation is nearly geostrophic, but is not affected by the bottom topography in the deep bay. It is suggested that intense surface water exchange through the bay mouth occurs in winter, whereas it is not active in the other seasons when no significant vorticity is supplied on the bay mouth from the atmosphere. Moreover, we propose a hypothesis that the atmospheric wind stress curl will cause the frequent appearance of the counterclockwise circulation in winter in the real ocean.     

NATURE OF PRECIPITATION AND ACTIVITY OF CUMULUS CONVECTION DURING THE 1991 MEIYU SEASON OF CHANGJIANG-HUAIHE RIVER BASIN

Seasonal variability regarding the nature of precipitation and the activity of cumulus convectionduring the 1991 Meiyu season of Changjiang-Huaihe River Basin(Jianghuai)has been investigatedby calculating apparent heat source/apparent moisture sink and analyzing TBB(cloud-topblackbody radiation temperature)data.It is found that three periods of strong ascending motionduring the Meiyu season lead to three episodes of heavy rain,and the latent heat due to theprecipitation is of the sole heat source of the atmosphere.The nature of precipitation showsdistinct seasonal variability,from frontal precipitation of the first episode to the extremely strongconvective precipitation of the third episode.TBB field of East Asia may well reflect not only theintensity of convection and rainfall,but also the movement of rain belt and convection belt.In thewhole Meiyu season.convection belt mainly stays in Jianghuai.but may shift within the domain ofEast Asia.Its locating in Jianghuai or not determines the maintenance or break of Meiyu.In thethird episode,the narrow convection belt over Jianghuai is mainly caused by southwest monsoonwhich takes moist and convective atmosphere from tropical ocean.     

Development of a Multi-Layer Urban Canopy Model for the Analysis of Energy Consumption in a Big City: Structure of the Urban Canopy Model and its Basic Performance

A multilayer one-dimensional canopy model was developed to analyze the relationship between urban warming and the increase in energy consumption in a big city. The canopy model, which consists of one-dimensional diffusion equations with a drag force, has three major parameters: building width, distance between buildings, and vertical floor density distribution, which is the distribution of a ratio of the number of the buildings that are taller than some level to all the buildings in the area under consideration. In addition, a simplified radiative process in the canopy is introduced. Both the drag force of the buildings and the radiative process depend on the floor density distribution. The thermal characteristics of an urban canopy including the effects of anthropogenic heat are very complicated. Therefore, the focus of this research is mainly on the basic performance of an urban canopy without anthropogenic heat. First, the basic thermal characteristics of the urban canopy alone were investigated. The canopy model was then connected with a three-dimensional mesoscale meteorological model, and on-line calculations were performed for 10 and 11 August, 2002 in Tokyo, Japan. The temperature near the ground surface at the bottom of the canopy was considerably improved by the calculation with the canopy model. However, a small difference remained between the calculation and the observation for minimum temperature. Deceleration of the wind was well reproduced for the velocity at the top of the building by the calculation with the canopy model, in which the floor density distribution was considered.     

Characterization of Fe(III) (hydr)oxides in arsenic contaminated soil under various redox conditions by XAFS and Mössbauer spectroscopies

Characterization of Fe(III) (hydr)oxides in soils near the Ichinokawa mine was conducted using X-ray absorption fine structure (XAFS) and Mössbauer spectroscopies, and the structural changes were correlated with the release of As into pore-water. The Eh values decreased monotonically with depth. Iron is mainly present as poorly-ordered Fe(III) (hydr)oxides, such as ferrihydrite, over a wide redox range (from Eh = 360 to −140 mV). Structural details of the short-range order of these Fe(III) (hydr)oxides were examined using Mössbauer spectroscopy by comparing the soil phases with synthesized ferrihydrite samples having varying crystallinities. The crystallinity of the soil Fe (hydr)oxides decreased slightly with depth and Eh. Thus, within the redox range of this soil profile, ferrihydrite dominated, even under very reducing conditions, but the crystalline domain size, and, potentially, particle size, changed with the variation in Eh. In the soil–water system examined here, where As concentration and the As(III)/As(V) ratio in soil water increased with depth, ferrihydrite persisted and maintained or even enhanced its capacity for As retention with increased reducing conditions. Therefore, it is concluded that As release from these soils largely depends on the transformation of As(V) to As(III) rather than reductive dissolution of Fe(III) (hydr)oxide.     

Chemical and structural control of the partitioning of Co, Ce, and Pb in marine ferromanganese oxides

The oxidation state and mineral phase association of Co, Ce, and Pb in hydrogenetic, diagenetic, and hydrothermal marine ferromanganese oxides were characterized by X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopy and chemical extraction. Cobalt is trivalent and associated exclusively with the Mn oxide component (vernadite). Cerium is tetravalent in all genetic-type oxides (detection limit for Ce(III) ∼ 5 at. %), including Fe-rich areas (ferrihydrite) of hydrogenetic oxides, and is associated primarily with vernadite. Thus, the extent of a Ce anomaly does not result from variations in redox conditions, but appears to be kinetically controlled, decreasing when the growth rate increases from hydrogenetic to diagenetic to hydrothermal oxides. Lead is divalent and associated with Mn and Fe oxides in variable proportions. According to EXAFS data, Pb is mostly sorbed on edge sites at chain terminations in Fe oxide and at layer edges in Mn oxide (ES complex), and also on interlayer vacancy sites in Mn oxide (TCS complex). Sequential leaching experiments, spectroscopic data, and electrochemical considerations suggest that the geochemical partitioning in favor of the Mn oxide component decreases from Co to Ce to Pb, and depends on their oxidative scavenging by Mn and Fe oxides.     

Geology,Alteration, and Mineralization of the Kay Tanda Epithermal Gold Deposit,Lobo, Batangas,Philippines

The Kay Tanda epithermal Au deposit in Lobo, Batangas is one of the Au deposits situated in the Batangas Mineral District in southern Luzon, Philippines. This study aims to document the geological, alteration, and mineralization characteristics and to determine the age of the mineralization, the mechanism of ore deposition, and the hydrothermal fluid characteristics of the Kay Tanda deposit. The geology of Kay Tanda consists of (i) the Talahib Volcanic Sequence, a Middle Miocene dacitic to andesitic volcaniclastic sequence that served as the host rock of the mineralization; (ii) the Balibago Diorite Complex, a cogenetic intrusive complex intruding the Talahib Volcanic Sequence; (iii) the Calatagan Formation, a Late Miocene to Early Pliocene volcanosedimentary formation unconformably overlying the Talahib Volcanic Sequence; (iv) the Dacite Porphyry Intrusives, which intruded the older lithological units; and (v) the Balibago Andesite, a Pliocene postmineralization volcaniclastic unit. K‐Ar dating on illite collected from the alteration haloes around quartz veins demonstrated that the age of mineralization is around 5.9 ± 0.2 to 5.5 ± 0.2 Ma (Late Miocene). Two main styles of mineralization are identified in Kay Tanda. The first style is an early‐stage extensive epithermal mineralization characterized by stratabound Au‐Ag‐bearing quartz stockworks hosted at the shallower levels of the Talahib Volcanic Sequence. The second style is a late‐stage base metal (Zn, Pb, and Cu) epithermal mineralization with local bonanza‐grade Au mineralization hosted in veins and hydrothermal breccias that are intersected at deeper levels of the Talahib Volcanic Sequence and at the shallower levels of the Balibago Intrusive Complex. Paragenetic studies on the mineralization in Kay Tanda defined six stages of mineralization; the first two belong to the first mineralization style, while the last four belong to the second mineralization style. Stage 1 is composed of quartz ± pyrophyllite ± dickite/kaolinite ± diaspore alteration, which is cut by quartz veins. Stage 2 is composed of Au‐Ag‐bearing quartz stockworks associated with pervasive illite ± quartz ± smectite ± kaolinite alteration. Stage 3 is composed of carbonate veins with minor base metal sulfides. Stage 4 is composed of quartz ± adularia ± calcite veins and hydrothermal breccias, hosting the main base metal and bonanza‐grade Au mineralization, and is associated with chlorite‐illite‐quartz alteration. Stage 5 is composed of epidote‐carbonate veins associated with epidote‐calcite‐chlorite alteration. Stage 6 is composed of anhydrite‐gypsum veins with minor base metal mineralization. The alteration assemblage of the deposit evolved from an acidic mineral assemblage caused by the condensation of magmatic volatiles from the Balibago Intrusive Complex into the groundwater to a slightly acidic mineral assemblage caused by the interaction of the host rocks and the circulating hydrothermal waters being heated up by the Dacite Porphyry Intrusives to a near‐neutral pH toward the later parts of the mineralization. Fluid inclusion microthermometry indicates that the temperature of the system started to increase during Stage 1 (T = 220–250°C) and remained at high temperatures (T = 250–290°C) toward Stage 6 due to the continuous intrusion of Dacite Porphyry Intrusives at depth. Salinity slightly decreased toward the later stages due to the contribution of more meteoric waters into the hydrothermal system. Boiling is considered the main mechanism of ore deposition based on the occurrence of rhombic adularia, the heterogeneous trapping of fluid inclusions of variable liquid–vapor ratios, the distribution of homogenization temperatures, and the gas ratios obtained from the quantitative fluid inclusion gas analysis of quartz. Ore mineral assemblage and sulfur fugacity determined from the FeS content of sphalerite at temperatures estimated by fluid inclusion microthermometry indicate that the base metal mineralization at Kay Tanda evolved from a high sulfidation to an intermediate sulfidation condition.     

Direct observation of Cm(III)-fulvate species on fulvic acid-montmorillonite hybrid by laser-induced fluorescence spectroscopy

Particulate matter plays an important role in the removal of metal ions from water in natural aquifers. Some of the most important of these materials consist of associations of inorganic particles (clay minerals, oxides) with humic substances, associations that can form readily in such an environment due to the strong affinity between inorganic particles and humic substances. These associations are referred to in this paper as organic-inorganic hybrids. However, it is not clear whether the sorbed species of metal ions in such organic-inorganic hybrids are organic or inorganic species because of the complexity of such hybrids and the lack of appropriate methods for characterizing the trace metal ions incorporated in them. In this study, laser-induced fluorescence spectroscopy (LIF) was used successfully to characterize the Cm(III) species on an FA(fulvic acid)-montmorillonite hybrid, an example of such organic-inorganic hybrids. The LIF clearly showed that Cm(III) can be sorbed as Cm(III)-fulvate complex in the FA-montmorillonite hybrid. These results were consistent with those of experiments of solid-water partitioning of Cm(III) (or Eu(III) used as an analogue) and speciation calculations based on the stability constants of Cm(III)-fulvate complexes determined in this study. The results of LIF and the partitioning experiments showed that the solid-water distribution of humic substances governed that of Cm(III) under our experimental conditions. The Cm(III) preference for forming Cm(III)-fulvate complexes was also evident under a condition that would be found in a natural aquifer with a fairly low concentration of organic matter in freshwater (dissolved organic carbon: 2 mg/dm³), as determined by our speciation calculations. These findings on the importance of humic substances in the migration of Cm(III) indicate that the clarification of the environmental behavior of humic substances is necessary to understand fully the behavior of Cm(III), or actinide(III) and lanthanide(III) ions, in natural aquifers.     

中国东南部与日本中—新生代构造-岩浆作用对比研究

重点讨论了中国东南部和日本中、新生代火成岩的时空分布及其构造环境,总结了两者的异同性。印支期和燕山早期（190～170Ma）中国东南部和日本具有不同的岩浆活动演化史。在165～150Ma期间,中国东南部广泛分布有过铝和弱过铝的S型花岗岩,而170～130Ma则为日本岩浆活动沉寂期。燕山晚期,中国东南部和日本都发生大规模的火山-侵入活动,同是库拉-太平洋板块向欧亚大陆俯冲-碰撞及其后伸展-裂解的产物,日本开始时代晚（130Ma）,并一直持续到始新世（45Ma）。进入喜马拉雅期,在日本海打开之前（>15Ma）,中国东南部和日本同处于大陆伸展构造环境,在日本海打开之后（<15Ma）,中国东南部和日本进入完全不同的构造演化阶段。     

Fluid Inclusion and Stable Isotope Study at the Southeastern Martabe Deposit: Purnama,Barani and Horas Ore Bodies,North Sumatra,Indonesia

The Martabe Au–Ag deposit, North Sumatra Province, Indonesia, is a high sulfidation epithermal deposit, which is hosted by Neogene sandstone, siltstone, volcanic breccia, and andesite to basaltic andesite of Angkola Formation. The deposit consists of six ore bodies that occurred as silicified massive ore (enargite–luzonite–pyrite–tetrahedrite–tellurides), quartz veins (tetrahedrite–galena–sphalerite–chalcopyrite), banded sulfide veins (pyrite–tetrahedrite–sphalerite–galena) and cavity filling. All ore bodies are controlled by N–S and NW–SE trending faults. The Barani and Horas ore bodies are located in the southeast of the Purnama ore body. Fluid inclusion microthermometry, and alunite‐pyrite and barite‐pyrite pairs sulfur isotopic geothermometry show slightly different formation temperatures among the ore bodies. Formation temperature and salinity of fluid inclusions of the Purnama ore body range from 200 to 260 C and from 6 to 8 wt.% NaCl equivalent, respectively. Formation temperature and salinity of fluid inclusions of the Barani ore body range from 200 to 220 °C and from 0 to 2.5 wt.% NaCl equivalent and those of the Horas ore body range from 240 to 275 °C and from 2 to 3 wt.% NaCl equivalent, respectively. The Barani and Horas ore bodies are less silicified and sulfides are less abundant than the Purnama ore body. A relationship between enthalpy and chloride content indicates mixing of hot saline fluids with cooler dilute fluids during the mineralization of each of the ore bodies. The δ¹⁸O values of quartz samples from the southeast ore bodies exhibit a wide range from +4.2 to +12.9‰ with an average value of +7.0‰. The δ¹⁸O values of H₂O estimated from δ¹⁸O values of quartz, barite and calcite confirm the oxygen isotopic shift to near meteoric water trend, which support the incorporation of meteoric water. Salinity of the fluid inclusions decrease from >5 wt.% NaCl equivalent in the Purnama ore body to <3 wt.% NaCl equivalent in the Barani ore body, indicating different fluid systems during mineralization. The δ³⁴S values of sulfide and sulfate in Purnama range from ? 4.2 to +5.5‰ and from +1.2 to +26.7‰, those in the Barani range from ? 4.3 to +26.4‰ and from +3.9 to +18.5‰ and those in the Horas ore body range from ? 11.8 to +3.5‰ and from +1.4 to +25.7‰, respectively. The δ³⁴S of total bulk sulfur in southeastern ore bodies (Σδ³⁴S) was estimated to be approximately +6‰. The estimated sulfur fugacity during formation of the Purnama and Horas ore bodies is relatively high. It was between 10^?4.8 and 10^?10.8 atm at 220 to 260 °C. Tellurium fugacity was between 10^?7.8 and 10^?9.5 atm at 260 °C and between 10^?9 and 10^?10.6 atm at 220 °C in the Purnama ore body. The Barani ore body was formed at lower fS₂, lower than about 10^?14 atm at 200 to 220 °C based on the presence of arsenopyrite and pyrrhotite in the early stage, and between 10^?14 and 10^?12 atm based on the existence of enargite and tennantite in the last stage. © 2016 The Society of Resource Geology