The first absolute gravity measurements in Indonesia

For the purposes of the calibration of the superconducting gravimeter (SG) in Bandung and the establishment of the absolute gravity (AG) points, we carried out AG measurements for the first time in Indonesia in November 2002. The measurements in Bandung were conducted between November 15th and 20th by means of a FG5 (#210), and 14,520 effective drops were obtained. The gravity value newly determined at the AG point in Bandung is 977976701.2 μgal (1 μgal = 10⁻⁸ ms⁻²) and the scale factor for the SG is −52.22 μgal/V. We also established another AG point in Yogyakarta near Merapi volcano and carried out AG measurements in Yogyakarta between November 22nd and 26th. The gravity value determined for this station is 978203093.5 μgal.     

Formation Process of Zircon Associated with REE‐Fluorocarbonate and Niobium Minerals in the Nechalacho REE Deposit,Thor Lake,Canada

The two drill holes, which penetrated sub‐horizontal rare earth element (REE) ore units at the Nechalacho REE in the Proterozoic Thor Lake syenite, Canada, were studied in order to clarify the enrichment mechanism of the high‐field‐strength elements (HFSE: Zr, Nb and REE). The REE ore units occur in the albitized and potassic altered miaskitic syenite. Zircon is the most common REE mineral in the REE ore units, and is divided into five types as follows: Type‐1 zircon occurs as discrete grains in phlogopite, and has a chemical character similar to igneous zircon. Type‐2 zircon consists of a porous HREE‐rich core and LREE–Nb–F‐rich rim. Enrichment of F in the rim of type‐2 zircon suggests that F was related to the enrichment of HFSE. The core of type‐2 zircon is regarded to be magmatic and the rim to be hydrothermal in origin. Type‐3 zircon is characterized by euhedral to anhedral crystals, which occur in a complex intergrowth with REE fluorocarbonates. Type‐3 zircon has high REE, Nb and F contents. Type‐4 zircon consists of porous‐core and ‐rim, but their chemical compositions are similar to each other. This zircon is a subhedral crystal rimmed by fergusonite. Type‐5 zircon is characterized by smaller, porous and subhedral to anhedral crystals. The interstices between small zircon grains are filled by fergusonite. Type‐4 and type‐5 zircon grains have low REE, Nb and F contents. Type‐1 zircon is only included in one unit, which is less hydrothermally altered and mineralized. Type‐2 and type‐3 zircon grains mainly occur in the shallow units, while those of type‐4 and type‐5 are found in the deep units. The deep units have high HFSE contents and strongly altered mineral textures (type‐4 and type‐5) compared to the shallow units. Occurrences of these five types of zircon are different according to the depth and degree of the hydrothermal alteration by solutions rich in F and CO₃, which permit a model for the evolution of the zircon crystallization in the Nechalacho REE deposit as follows: (i) type‐1 (discrete magmatic zircon) is formed in miaskitic syenite. (ii) LREE–Nb–F‐rich hydrothermal zircon formed around HREE‐rich magmatic zircon (type‐2). (iii) type‐3 zircon crystallized through the F and CO₃‐rich hydrothermal alteration of type‐2 zircon which formed the complex intergrowth with REE fluorocarbonates; (iv) the CO₃‐rich hydrothermal fluid corroded type‐3, forming REE–Nb‐poor zircon (type‐4). Niobium and REE were no longer stable in the zircon structure and crystallized as fergusonite around the REE–Nb‐leached zircon (type‐4); (v) type‐5 zircon is formed by the more CO₃‐rich hydrothermal alteration of type‐4 zircon, suggested by the fact that type‐4 and type‐5 zircon grains are often included in ankerite. Type‐3 to type‐5 zircon grains at the Nechalacho REE deposit were continuously formed by leaching and/or dissolution of type‐2 zircon in the presence of F‐ and/or CO₃‐rich hydrothermal fluid. These mineral associations indicate that three representative hydrothermal stages were present and related to HFSE enrichment in the Nechalacho REE deposit: (i) F‐rich hydrothermal stage caused the crystallization of REE–Nb‐rich zircon (type‐2 rim and type‐3), with abundant formation of phlogopite and fluorite; (ii) F‐ and CO₃‐rich hydrothermal stage led to the replacement of a part of REE–Nb–F‐rich zircon by REE fluorocarbonate; and (iii) CO₃‐rich hydrothermal stage resulted in crystallization of the REE–Nb–F‐poor zircon and fergusonite, with ankerite. REE and Nb in hydrothermal fluid at the Nechalacho REE deposit were finally concentrated into fergusonite by way of REE–Nb–F‐rich zircon in the hydrothermally altered units.     

Upper Cretaceous depositional environments and bivalve assemblages of far-east Asia: the Himenoura Group, Kyushu, Japan

The depositional environments and bivalve assemblages are determined for the Upper Cretaceous Hinoshima Formation of the Himenoura Group, Kamishima, Amakusa Islands, Kyushu, Japan. The Hinoshima Formation is characterized by a thick transgressive succession that varies from incised-valley-fill deposits to submarine slope deposits with high aggradation rates of depositional systems. The incised valley is filled with fluvial, bayhead delta, brackish-water estuary, and marine embayment deposits, and is overlain by thick slope deposits.Shallow marine bivalves are grouped into five fossil assemblages according to species composition: Glycymeris amakusensis (foreset beds of a bayhead delta), Nippononectes tamurai (foreset beds of a bayhead delta), Ezonuculana mactraeformis–Nucula formosa (central bay), Glycymeris amakusensis–Apiotrigonia minor (slope), and Inoceramus higoensis–Parvamussium yubarensis (slope). These bivalve assemblages all represent autochthonous and parautochthonous conditions except for a Glycymeris amakusensis–Apiotrigonia minor assemblage found in debris flow and slump deposits. The life habitats of these bivalves and the compositions of the assemblages are discussed in terms of the ecological history of fossil bivalves of the mid- to Late Cretaceous.     

Geochemical Characteristics of Apatite in Heavy REE‐rich Deep‐Sea Mud from Minami‐Torishima Area,Southeastern Japan

We have conducted geochemical and mineralogical investigations of the rare earth and yttrium (REY)‐rich mud from the Minami‐Torishima area in the Pacific in order to clarify the concentration of REY and their host‐phase in the mud. X‐ray diffraction analysis shows that the mud is mainly composed of phillipsite, fluorapatite, quartz, albite, illite and montmorillonite. Whole‐rock CaO, P₂O₅ and total REY contents of the mud are positively correlated. Relative abundance of apatite is also positively correlated to P₂O₅ and total REY contents. These correlations suggest that apatite is the main host of the P₂O₅ and REY in the mud. We make in situ compositional analyses of constituent minerals in the REY mud. The results show that the apatite is abundant in REY (9300–32,000 ppm) and is characterized by a negative Ce anomaly and enrichment in heavy rare‐earth elements. This abundance and composition of REY of the mud is similar those of fish debris apatites. In contrast, phillipsite is less abundant in REY (60–170 ppm). Therefore we conclude that the main REY host phase of the mud is apatite.     

Studying the Experience of Solving Water Supply Problems in the Medieval Crimea (Sudak XIV–XV Centuries)

Water Resources - Archeological and geological data on solving the problems of water supply and water use in the medieval Sougdeia (Sudak Town in the XIV–XV centuries) are generalized and...