Optical properties of the red tide in Isahaya Bay,southwestern Japan: Influence of chlorophyll a concentration

Remote sensing reflectance [R _rs(λ)] and absorption coefficients of red tides were measured in Isahaya Bay, southwestern Japan, to investigate differences in the optical properties of red tide and non-red tide waters. We defined colored areas of the sea surface, visualized from shipboard, as “red tides”. Peaks of the R _rs(λ) spectra of non-red tide waters were at 565 nm, while those of red tides shifted to longer wavelengths (589 nm). The spectral shape of R _rs(λ) was close to that of the reciprocal of the total absorption coefficient [1/a(λ)], implying that the R _rs(λ) peak is determined by absorption. Absorption coefficients of phytoplankton [a _ph(λ)], non-pigment particles and colored dissolved organic matter increased with increasing chlorophyll a concentration (Chl a), and those coefficients were correlated with Chl a for both red tide and non-red tide waters. Using these relationships between absorption coefficients and Chl a, variation in the spectrum of 1/a(λ) as a function of Chl a was calculated. The peak of 1/a(λ) shifted to longer wavelengths with increasing Chl a. Furthermore, the relative contribution of a _ph(λ) to the total absorption in red tide water was significantly higher than in non-red tide water in the wavelength range 550–600 nm, including the peak. Our results show that the variation of a _ph(λ) with Chl a dominates the behavior of the R _rs(λ) peak, and utilization of R _rs(λ) peaks at 589 and 565 nm may be useful to discriminate between red tide and non-red tide waters by remote sensing.     

Fluid Inclusion Study and Opaque Mineral Assemblage at the Deep and Shallow Part of the Batu Hijau Porphyry Copper-gold Deposit, Sumbawa, Indonesia

The Batu Hijau deposit is the only porphyry type deposit in production in the Sunda‐Banda arc, Indonesia. This study discusses the reason for the localization of copper grade at the deep part of the deposit based on the observation of opaque mineral assemblage. In addition, the formation condition of quartz veins and opaque minerals is discussed on the basis of the fluid inclusion microthermometry. Samples were selected from drill holes SBD100, SBD168, SBD194, SBD254, and SBD257 to cover the wide vertical range. At the Batu Hijau deposit, quartz veins have been classified mainly into four types called A, B, C and D veins, and the A veins contain mainly bornite, often associated with digenite and chalcocite. In addition, magnetite occurs in A veins. However, at the deep part of the deposit, there are quartz veins associated with magnetite, but few copper sulfides such as bornite and chalcopyrite in quartz veins, as observed in SBD257. Quartz veins at depth in SBD257 have abundant magnetite and pyrite. Pyrite in quartz veins at depth in SBD257 mainly occur at the rim of magnetite grains or interstices between them. In quartz veins in SBD254, there are abundant copper sulfides such as bornite and chalcopyrite in spite of the depth. Bornite and chalcopyrite occur as inclusions in magnetite grains in quartz veins in SBD254. Pyrite which often occurs in low grade zone in quartz veins in SBD254 is also recognized at the rims of copper sulfides. This indicates that pyrite in SBD257 and SBD254 formed later than magnetite. On the other hand, blebs of bornite and chalcopyrite inclusions in magnetite grains, which are recognized in quartz veins in SBD168 at shallow high grade part, suggest that the hydrothermal fluid, from which magnetite was deposited also brought the copper sulfides such as bornite and chalcopyrite to the deep part of the Batu Hijau deposit. Therefore, it is concluded that initially the high grade ore zone extended to depth without localization. However due to the later overprinting hydrothermal activity, copper sulfides and magnetite were replaced or dissolved and pyrite was formed, resulting the low grade zone at the deep part of the deposit. Dissolution temperatures (Td) of halite obtained by from fluid inclusion microthermometry show significant differences between SBD168 and other drill holes. The high Td obtained in SBD168 may indicate larger volume of NaCl crystals in hydrothermal fluid at the time of entrapment of the fluid inclusions and formation of other opaque minerals such as magnetite and copper‐iron sulfides. It suggests that the ratio of vapor to brine is also higher at the shallow part of the deposit. The higher vapor to brine ratio may suggest a higher degree of boiling. Removal of vapor phase separated from brine during boiling increases the concentration of substances dissolved in the brine, and this will result in saturation, as evidenced by the salinity and NaCl saturation. The higher degree of boiling suggested by the higher vapor to brine ratio at shallow part may have increased the copper concentration in the brine that may have lead the saturation, resulted in the deposition of copper‐bearing minerals.     

地质聚合物技术的发展近况

概要介绍了一种无机聚合物———地质聚合物。首先对地质聚合物材料的制备过程作了介绍。根据原料的不同,地质聚合物材料的制备可以有两种途径:一种是以偏高岭石为基础原料,一种是以粉煤灰为主要原料。通常以硅酸钠水溶液作为单体硅源,氢氧化钠溶液作为碱激发剂以提高原料的溶出性。对某些在常温和低于100 ℃下制备的独石材料作了介绍。对煅烧高岭石,叶蜡石,粉煤灰和钢渣的溶出特性作了阐述。应用SEM EDX,对以粉煤灰为原料的地质聚合物材料的化学组成作了分析。最后对地质聚合物材料的经济性以及在环境保护等领域的应用前景,特别是在减少二氧化碳排放与废弃物处理方面的意义作了介绍。     

Evolution of Hydrothermal System at the Dizon Porphyry Cu-Au Deposit, Zambales, Philippines

Abstract. Evolution of hydrothermal system from initial porphyry Cu mineralization to overlapping epithermal system at the Dizon porphyry Cu‐Au deposit in western central Luzon, Zambales, Philippines, is documented in terms of mineral paragen‐esis, fluid inclusion petrography and microthermometry, and sulfur isotope systematics. The paragenetic stages throughout the deposit are summarized as follows; 1) stockwork amethystic quartz veinlets associated with chalcopyrite, bornite, magnetite and Au enveloped by chlorite alteration overprinting biotite alteration, 2) stockwork quartz veinlets with chalcopyrite and pyrite associated with Au and chalcopyrite and pyrite stringers in sericite alteration, 3) stringer quartz veinlets associated with molybdenite in sericite alteration, and 4) WNW‐trending quartz veins associated with sphalerite and galena at deeper part, while enargite and stibnite at shallower levels associated with advanced argillic alteration. Chalcopyrite and bornite associated with magnetite in quartz veinlet stockwork (stage 1) have precipitated initially as intermediate solid solution (iss) and bornite solid solution (bnss), respectively. Fluid inclusions in the stockwork veinlet quartz consist of gas‐rich inclusions and polyphase inclusions. Halite in polyphase inclusions dissolves at temperatures ranging from 360d?C to >500d?C but liquid (brine) and gas (vapor) do not homogenize at <500d?C. The maximum pressure and minimum temperature during the deposition of iss and bnss with stockwork quartz veinlets are estimated to be 460 bars and 500d?C. Fluid inclusions in veinlet stockwork quartz enveloped in sericite alteration (stage 2) consist mainly of gas‐rich inclusions and polyphase inclusions. In addition to the possible presence of saturated NaCl crystals at the time of entrapment of fluid inclusions that exhibit the liquid‐vapor homogenization temperatures lower than the halite dissolution temperatures in some samples, wide range of temperatures of halite dissolution and liquid‐vapor homogenization of polyphase inclusions from 230d?C to >500d?C and from 270d?C to >500d?C, respectively, suggests heterogeneous entrapment of gaseous vapor and hypersaline brine. The minimum pressure and temperature are estimated to be about 25 bars and 245d?C. Fluid inclusions in veinlet quartz associated with molybdenite (stage 3) are dominated by gas‐rich inclusions accompanied with minor liquid‐rich inclusions that homogenize at temperatures between 350d?C and 490d?C. Fluid inclusions in vuggy veinlet quartz associated with stibnite (stage 4) consist mainly of gas‐rich inclusions with subordinate polyphase inclusions that do not homogenize below 500d?C. Fluid inclusions in veinlet quartz associated with galena and sphalerite (stage 4) are composed of liquid‐rich two‐phase inclusions, and they homogenize into liquid phase at temperatures ranging widely from 190d?C to 300d?C (suggesting boiling) and the salinity ranges from 1.0 wt% to 3.4 wt% NaCl equivalent. A pressure of about 15 bars is estimated for the dilute aqueous solution of 190d?C from which veinlet quartz associated with galena and sphalerite precipitated. In addition to a change in temperature‐pressure regime from lithostatic pressure during the deposition of iss and bnss with stockwork quartz veinlets to hydrostatic pressure during fracture‐controlled quartz veinlet associated with galena and sphalerite, a decrease in pressure is supposed to have occurred due to unroofing or removal of the overlying piles during the temperature decrease in the evolution of hydrothermal system. The majority of the sulfur isotopic composition of sulfides ranges from ±0 % to +5 %. Sulfur originated from an iso‐topically uniform and homogeneous source, and the mineralization occurred in a single hydrothermal system.     

Experimental study on the velocity of fragments in collisional breakup

The motion of fragments following a catastrophic destruction by either a normal or an oblique impact at 2.5–2.9 km sec^?1 into cubic and spherical basalt targets was studied with a high-speed framing camera. Velocities at the antipodes of the targets vary as (E/M)^0.75 (E = impact energy; M = target mass) and are lower than 200 m sec^?1 at E/M ? 10⁹ ergs g^?1. Excluding fine-grained particles from the impact site, 70 to 80% by mass fraction of the fragments have velocities lower than twice the antipodal velocity. Comminution and ejection energies wasted in this mass fraction were a few percent of the impact energy at E/M ? 5 × 10⁷ ergs g^?1. During a catastrophic impact into asteroids some of the fragmented bodies can be reconcentrated by mutual gravitation.     

Active spreading and hydrothermalism in North Fiji Basin (SW Pacific). Results of Japanese French Cruise Kaiyo 87

The aim of the Japanese-French Kaiyo 87 cruise was the study of the spreading axis in the North Fiji Basin (SW Pacific). A Seabeam and geophysical survey allowed us to define the detailed structure of the active NS spreading axis between 16° and 22° S and its relationships with the left lateral motion of the North Fiji Fracture Zone. Between 21° S and 18°10′ S, the spreading axis trends NS. From 18°10 S to 16°40 S the orientation of the spreading axis changes from NS to 015°. North of 16°40′ S the spreading axis trends 160°. These two 015° and 160° branches converge with the left lateral North Fiji fracture zone around 16°40′ S to define an RRFZ triple junction. Water sampling, dredging and photo TV deep towing give new information concerning the hydrothermal activity along the spreading axis. The discovery of hydrothermal deposits associated with living communities confirms this activity.     

Deposition Rates of Terrestrial and Marine Organic Carbon in the Osaka Bay, Seto Inland Sea, Japan, Determined Using Carbon and Nitrogen Stable Isotope Ratios in the Sediment

Carbon and nitrogen stable isotope ratios (¹³C and ¹⁵N) of surface sediments were measured within Osaka Bay, in the Seto Inland Sea in Japan, in order to better understand the sedimentation processes operating on both terrestrial and marine organic matter in the Bay. The ¹³C and ¹⁵N of surface sediments in the estuary of the Yodo River were less than –23 and 5 respectively, but increased in the area up to about 10 km from the river mouth. At greater distances they became constant (giving ¹³C of about –20 and ¹⁵N about 6). It can be concluded that large amounts of terrestrial organic matter exist near the mouth of the Yodo River. Stable isotope ratios in the estuary of the Yodo River within 10 km of the river mouth were useful indicators allowing study of the movement of terrestrial organic matter. Deposition rates for total organic carbon (TOC) and total nitrogen (TN) over the whole of the Bay were estimated to be 63,100 ton C/year and 7,590 ton N/year, respectively. The deposition rate of terrestrial organic carbon was estimated to be 13,200 (range 2,000–21,500) ton C/year for the whole of Osaka Bay, and terrestrial organic carbon was estimated to be about 21% (range 3–34) of the TOC deposition rate. The ratio of the deposition rate of terrestrial organic carbon to the rate inflow of riverine TOC and particulate organic carbon (POC) were estimated to be 19% (range 3–31) and 76% (range 12–100), respectively.     

Metallogenesis of Porphyry Cu Deposits of the Western Luzon Arc, Philippines: K-Ar ages, SO3 Contents of Microphenocrystic Apatite and Significance of Intrusive Rocks

Abstract: K–Ar ages of the following porphyry Cu deposits in the western Luzon arc are determined: Lobo-Boneng (10.50.4 Ma), Santo Niño (9.50.3 Ma), Black Mountain (2.10.1 Ma), Dizon (2.50.2 Ma) and Taysan (7.30.2 Ma). Microphenocrys-tic apatite in the late Cenozoic intermediate to silicic intrusions associated with porphyry Cu deposits in the western Luzon arc contains sulfur as SO₃ detectable by electron probe microanalyzer. Sulfur is supposed to have been accommodated dominantly as oxidized species in oxidizing hydrous magmas that generated porphyry Cu deposits. Likewise, such high SO₃ contents in microphenocrystic apatite are common characteristics of the intermediate to silicic magmatism of the western Luzon arc, from tonalitic rocks of the Luzon Central Cordillera of about 15 Ma to an active magmatism at Mount Pinatubo. Thus, the western Luzon arc has been generating porphyry Cu mineralization associated with oxidizing hydrous intermediate to silicic magmatism related to eastward subduction, since Miocene to the present day. Intermediate to silicic rocks since 15 Ma to present-day western Luzon arc generally show high whole-rock Sr/Y ratio ranging from 20 to 184. However, porphyry Cu deposit is not necessarily related to the rocks that show higher Sr/Y ratios compared to the other barren rocks in the western Luzon arc. The characteristics of the intermediate to silicic magma associated with porphyry Cu deposit are not attributed to the composition of the source material of the magma, but to the properties defined by the high activity of oxidized species of sulfur in the fluid phase that is encountered during the generation of intermediate to silicic magmas.