Chemical evidence for the origin of the cold water belt along the northeastern coast of Hokkaido

In the southwestern Okhotsk Sea, the cold water belt (CWB) is frequently observed on satellite images offshore of the Soya Warm Current flowing along the northeastern coast of Hokkaido, Japan, during summertime. It has been speculated that the CWB is upwelling cold water that originates from either subsurface water of the Japan Sea off Sakhalin or bottom water of the Okhotsk Sea. Hydrographic and chemical observations (nutrients, humic-type fluorescence intensity, and iron) were conducted in the northern Japan Sea and southwestern Okhotsk Sea in early summer 2011 to clarify the origin of the CWB. Temperature–salinity relationships, vertical distributions of chemical components, profiles of chemical components against density, and the (NO₃ + NO₂)/PO₄ relationship confirm that water in the CWB predominantly originates from Japan Sea subsurface water.     

Petrography,geochemistry, and tectonics of a rifted fragment of Mainland Asia: evidence from the Lasala Formation,Mindoro Island,Philippines

Petrological and geochemical investigations of the sedimentary Lasala formation in northwest Mindoro, Philippines, offer new insights into the origin of this geologically contentious region. Mindoro island’s position at the boundary between Sundaland and the Philippine Mobile Belt has led to variable suggestions as to how much of it is continent derived or not. The Eocene Lasala formation overlies the Jurassic Halcon metamorphics, a regionally metamorphosed suite generally thought to have formed as a result of arc-continent collision processes. The sedimentary formation consists mainly of sandstones and shales interbedded with mudstones, basalt flows, and subordinate limestones and conglomerates. Petrographic information on the Lasala clastic rocks demonstrates a uniform framework composition that is predominantly quartzose. Major oxide, trace element abundances, and various elemental ratios similarly impart a strongly felsic signature. These characteristics are taken to indicate a chiefly continental, passive margin derivation and deposition of the Lasala sediments during the Eocene. The weak indication of active margin influence is suggested to be an inherited signature, supported by paleogeographic models of the southeastern Asian margin area during the pre-Cenozoic.     

Determination of Selenium in Fifty Two Geochemical Reference Materials by Hydride Generation Atomic Absorption Spectrometry

The selenium content of fifty two geochemical reference samples, issued by several reference material producers (ANRT, GIT-IWG, USGS, NIST and GSJ) has been determined by continuous hydride generation and atomic absorption spectrometry. Selenium(VI) in the digested solutions was pre-reduced to selenium(IV) by heating in 6 mol l⁻¹ HCl solution. The limit of detection was 3 ng g⁻¹ selenium in common geological samples. Some samples which contain a large amount of heavy metals were analysed by the standard addition technique. The agreement between the reported results and published data is satisfactory.     

Geochemical and mineralogical characteristics of ion-adsorption type REE mineralization in Phuket, Thailand

Geochemical and mineralogical studies were conducted on the 12-m-thick weathering profile of the Kata Beach granite in Phuket, Thailand, in order to reveal the transport and adsorption of rare earth elements (REE) related to the ion-adsorption type mineralization. The parent rock is ilmenite-series biotite granite with transitional characteristics from I type to S type, abundant in REE (592 ppm). REE are contained dominantly in fluorocarbonate as well as in allanite, titanite, apatite, and zircon. The chondrite-normalized REE pattern of the parent granite indicates enrichment of LREE relative to HREE and no significant Ce anomaly. The upper part of the weathering profile from the surface to 4.5 m depth is mostly characterized by positive Ce anomaly, showing lower REE contents ranging from 174 to 548 ppm and lower percentages of adsorbed REE from 34% to 68% compared with the parent granite. In contrast, the lower part of the profile from 4.5 to 12 m depth is characterized by negative Ce anomaly, showing higher REE contents ranging from 578 to 1,084 ppm and higher percentages from 53% to 85%. The negative Ce anomaly and enrichment of REE in the lower part of the profile suggest that acidic soil water in an oxidizing condition in the upper part mostly immobilized Ce⁴⁺ as CeO₂ and transported REE³⁺ downward to the lower part of the profile. The transported REE³⁺ were adsorbed onto weathering products or distributed to secondary minerals such as rhabdophane. The immobilization of REE results from the increase of pH due to the contact with higher pH groundwater. Since the majority of REE in the weathered granite are present in the ion-adsorption fraction with negative Ce anomaly, the percentages of adsorbed REE are positively correlated with the whole-rock negative Ce anomaly. The result of this study suggests that the ion-adsorption type REE mineralization is identified by the occurrence of easily soluble REE fluorocarbonate and whole-rock negative Ce anomaly of weathered granite. Although fractionation of REE in weathered granite is controlled by the occurrence of REE-bearing minerals and adsorption by weathering products, the ion-adsorption fraction tends to be enriched in LREE relative to weathered granite.     

Mineralogical and Geochemical Characteristics of the Utanobori Gold Deposit in Northern Hokkaido,Japan

The Utanobori gold deposit is a low‐sulfidation, epithermal vein‐type deposit located in northern Hokkaido, Japan. The deposit is hosted by conglomerate, sandstone, and tuff of the Middle to Late Miocene Esashi Formation. These rocks were hydrothermally altered. Silica sinters and quartz‐adularia veins are common in the deposit. The quartz‐adularia veins either contain a ginguro band, which corresponds to the main gold‐bearing vein (Type 1 Veins), or do not contain a ginguro band but contain minor adularia (Type 2 Veins). Type 1 Veins are divided into three stages with 12–14 substages. Ore minerals identified include electrum, naumannite, chlorargyrite, bromargyrite, an unidentified Fe‐Sb mineral, and an Fe‐(Sb)‐As mineral. These ore minerals formed in the main mineralization stages I (bands I‐b and I‐d) and II (band II‐a). Scanning electron microscopy with cathodoluminescence images show that cathodoluminescence‐dark microcrystalline quartz exhibiting colloform (ghost‐sphere) texture is closely associated with ore minerals in the Type 1 Vein and Type 2 Vein, and the Al and K contents of such quartz are commonly >1000 ppm. This indicates that the ore minerals were crystallized from alkaline, silica‐saturated fluids at temperatures <200°C, which initially deposited amorphous silica that was recrystallized to microcrystalline quartz. The average Au content of electrum is 52.5 at% Au (n = 10), 65.7 at% Au (n = 20), and 55.5 at% Au (n = 5) in bands I‐b, I‐d, and II‐a, respectively, of Type 1 Veins. The δ³⁴S_CDT values of two fine‐grained disseminated pyrites in the altered conglomerate and bedded tuff in the argillic altered zone are ?4.3 and ?4.2‰. Ar‐Ar dating on adularia yielded 13.6 ± 0.06 Ma, 13.6 ± 0.07 Ma, and 13.6 ± 0.06 Ma for the stages I, II, and III of the Type 1 Vein, respectively. K‐Ar ages determined on adularia in the silica sinter and on whole‐rock of glassy rhyolite of the Esashi Formation are 15.0 ± 0.4 Ma and 14.6 ± 0.4 Ma, respectively. These radiometric ages indicate that silica sinter associated with the rhyolitic volcanic rocks formed prior to the main gold mineralization.     

Rare Earth Elements in Hydrothermally Altered Granitic Rocks in the Ranong and Takua Pa Tin‐Field,Southern Thailand

Geochemical studies were conducted on the hydrothermally altered granitic rocks in the Ranong and Takua Pa tin‐fields in southern Thailand in order to investigate the mode of occurrence of REE (rare earth elements), with emphasis placed on a potential REE resource associated with granitic rocks in the Southeast Asian Tin Belt. The total REE (ΣREE) content of altered granitic rocks ranges from 130 to 350 ppm at Haad Son Paen (which is presently mined for kaolin clay) in the Ranong tin‐field, and that of altered granitic rocks and kaolinite veinlets reaches up to 424 ppm and 872 ppm, respectively, at Nok Hook in the Takua Pa tin‐field. Rare earth elements in the altered granitic rocks and kaolinite veinlets show a relatively flat chondrite‐normalized pattern, thus enriched in heavy REE compared with the original granitic rocks and their weathered crusts. At Nok Hook (Takua Pa), the ΣREE content of kaolinite separated from an altered granitic rock by elutriation is 1313 ppm, a ΣREE amount about four times higher than that of whole‐rock composition of the altered granitic rock. Chondrite‐normalized REE patterns of the elutriated kaolinite and of the altered granite are relatively flat. Sequential extraction experiments suggest that 41 and 85 percent of REE are present as ion exchangeable‐form in the altered granitic rock, and in the kaolinite veinlets, respectively. In addition, more than 90% of REE in the kaolinite veinlets are present as the acid‐soluble state. On the other hand, the ΣREE content of kaolinite veinlets and of the kaolinite concentrated by elutriation from an altered granitic rock at Haad Som Paen (Ranong) is 70 ppm and 75 ppm, respectively, thus enrichment of REE in kaolinite was not confirmed. In addition, by the sequential extraction experiments, 23% and 4% of REE were extracted from the altered granitic rock and the kaolinite veinlets at Haad Som Paen. In the altered granitic rocks at Haad Som Paen, REE are present as refractory phases, and REE in the acid‐soluble states had been leached by hydrothermal fluid.     

Victoria Carbonate-Base Metal Gold Deposit and Its Significance in the Mankayan Mineral District, Luzon, Philippines

Abstract. The Victoria gold deposit is a low-sulfidation style epithermal carbonate-base metal gold deposit discovered in 1995 in the Mankayan mineral district, northern Luzon, Philippines. It occurs just south of a high-sulfidation copper-gold orebody (Lepanto enargite deposit) and a porphyry copper-gold orebody (Far Southeast (FSE) deposit). Radiometric dating of the Victoria mineralization yields ages from 1.6 to 1.1 Ma, similar to ages of the Lepanto enargite deposit. Mineralogical, geochemical, fluid inclusion and sulfur isotope studies suggest that the Victoria deposit is not directly related to the late stage of hydrothermal activity that produced the FSE porphyry copper-gold and the Lepanto enargite deposits. The hydrothermal fluids from which Victoria was formed appear to have been derived from the south, and not from the FSE intrusive center to the northeast. This would suggest a regional south to north hydrothermal gradient, consistent with the similar flow within the FSE porphyry-Lepanto enargite system. On a district scale, structures similar to those of the Victoria deposit in trend and nature would be highly prospective, especially if they occur north of identified plutons and volcanic centers.     

Characteristics of Porphyry Cu Mineralization at Waisoi (Namosi District), Viti Levu, Fiji

The porphyry Cu deposits at Waisoi in Namosi district, Viti Levu are separated into two deposits: the Waisoi East deposit and the Waisoi West deposit. In the Waisoi East deposit, quartz porphyry is exposed and in the Waisoi West deposit, diorite porphyry is sporadically exposed in addition to a small body of quartz porphyry. The mineralization in the Waisoi East deposit is characterized by the bornite–chalcopyrite–pyrite assemblage associated with traces of molybdenite and native gold. Polyphase fluid inclusions in stockwork quartz veinlets show homogenization temperatures ranging from 210 to >500°C. The high‐grade Cu mineralization in the Waisoi West deposit is characterized by the bornite–chalcopyrite–pyrite assemblage accompanied with sheeted and stockwork quartz veinlets. Polyphase fluid inclusions occasionally containing hematite flakes in quartz veinlets in the center of the Waisoi West deposit homogenize at temperatures ranging from 450°C to >500°C. However, fluid inclusions in stockwork quartz veinlets in the periphery, homogenize at lower temperatures around 210°C. Both in the Waisoi East and Waisoi West deposits, primary bornite–chalcopyrite–pyrite assemblage in the high Cu‐grade zone was deposited at the upper stability limit of chalcopyrite with respect to sulfur fugacity. Thus, the principal Cu mineralization at the Waisoi deposits occurred at a relatively high sulfur fugacity, that is, in a high‐sulfidation environment.     

Content of plutonium,thorium and protactinium in sea water and recent coral in the North Pacific

The contents of plutonium isotopes (²³⁹Pu and²³⁸Pu), thorium isotopes (²³²Th,²³⁰Th and²²⁸Th) and protactinium-231 in sea water collected in the North Pacific, the East China Sea and the Japan Sea were determined. These nuclides were sequentially analyzed byα-ray spectrometry after separating them mainly with solvent extraction technique. The contents of²³⁹Pu in surface sea water ranged from 0.6 to 1.6 pCi/10001,²³⁸Pu/²³⁹Pu activity ratios being 0.2～0.7. The²²⁸Th/²³²Th activity ratios for the North Pacific waters varied between 7.6 and 30, whereas the sample from the East China Sea showed the very high value, 65. The contents of²³¹Pa are less than 6 percent of that in equilibrium with its parent²³⁵U. Furthermore, the analysis of plutonium isotopes in recent coral from Yoron Island was carried out and it was confirmed that plutonium isotopes have concentrated in recent coral with the concentration factor of about 1～2×10³.