Clinopyroxene on the join CaMgSi2O6-CaFe3+AlSiO6-CaTiAl2O6 at low oxygen fugacity

Subsolidus phase relations on the join CaMgSi₂O₆-CaFe³⁺ AlSiO₆-CaTiAl₂O₆ were studied by the ordinary quenching method at \(f_{O_2 } = 10^{ - 11} \) atm and 1,100°C. Crystalline phases encountered are clinopyroxene_ss (ss:solid solution) (Cpx_ss), melilite (Mel), perovskite (Pv), spinel_ss (Sp_ss), magnetite_ss (Mt_ss) and anorthite (An). There is no Cpx_ss single phase field, and the following assemblages were found; Cpx_ss+Mel, Cpx_ss+Mel+Sp_ss, Cpx_ss+Mel+Pv, Cpx_ss+Mel+Sp_ss+Pv, Cpx_ss+Pv+Sp_ss+An, Sp_ss+Pv+Mel+An+Cpx_ss, Mel+Mt_ss+An+Sp_ss+Cpx_ss+liquid and Mel+Mt_ss+An+Sp_ss+Cpx_ss+Pv. Mössbauer spectral study revealed that Cpx_ss contains both Fe²⁺ and Fe³⁺ in the octahedral site, and it was confirmed that the CaFe³⁺ AlSiO₆ content in the Cpx_ss at low \(f_{O_2 } \) is considerably less than that in the Cpx_ss crystallized in air, whereas the CaFe²⁺Si₂O₆ component increases. The maximum solubility of CaTlAl₂O₆ component in the Cpx_ss at low \(f_{O_2 } \) is higher than that in air. The decrease of CaFe³⁺ AlSiO₆ in the Cpx_ss at low \(f_{O_2 } \) may cause increase of CaTial₂O₆ in the Cpx_ss.     

The distribution of Fe3+ and Ga3+ between two tetrahedral sites in melilites,Ca2(Mg,Fe3+, Ga,Si)3O7

The distribution of Fe³⁺ and Ga³⁺ between the two tetrahedral sites in three synthetic melilites has been studied by using ⁵⁷Fe Mössbauer spectroscopy. In the melilite, (Ca₂Ga₂SiO₇)₅₀ (Ca₂Fe³⁺GaSiO₇)₅₀ (mol %), the distribution of Fe³⁺ and Ga³⁺ in T1 and T2 sites is apparently random, which can be explained in terms of the electrostatic valence rule. However in the melilites, (Ca₂MgSi₂O₇)₅₂ (Ca₂Fe³⁺GaSiO₇)₄₂ (Ca₂Ga₂SiO₇)₆ and (Ca₂MgSi₂O₇)₆₂ (Ca₂Fe³⁺GaSiO₇)₃₆ (Ca₂Ga₂SiO₇)₂ (mol %), Fe³⁺ shows preference for the more ionic T1 site and Ga³⁺ for the more covalent T2 site. If the electronegativity of Ga³⁺ is assumed to be larger than that of Fe³⁺, the mode of distribution of Fe³⁺ and Ga³⁺ can be explained in terms of our previous hypothesis that a large electronegativity induces a stronger preference for the more covalent T2 site.     

The bearing of the system CaMgSi2O6CaAl2SiO6CaFeAlSiO6 on fassaitic pyroxene

The system CaMgSi₂O₆CaAl₂SiO₆CaFeAlSiO₆ has been studied in air at 1 atm. The phase assemblage at subsolidus temperatures in the CaMgSi₂O₆-rich portion is Cpx + An + Mel and that in the CaMgSi₂O₆-poor portion Cpx + An + Mel + Sp. At subsolidus temperatures the sigle-phase field of clinopyroxene increases with an increase in the CaFeAlSiO₆ component of the system. The Al₂O₃ content of clinopyroxene, however, continues to increase beyond the single-phase field and attains at least 16.04 wt.% Al₂O₃ with 3.9 wt.% Fe₂O₃. The stability field of fassaite in the system over a range of pressures and oxygen fugacities has been estimated from data in the literature as well as the present data. The CaFeAlSiO₆ content of fassaite is dependent on oxygen fugacity, but is not influenced by pressure. The stability field is strongly influenced by oxygen fugacity at low and high pressure, and decreases with decreasing oxygen fugacity. Clinopyroxenes in both volcanic and metamorphic rocks from various localities, when plotted on the CaMgSi₂O₆CaAl₂SiO₆CaFeAlSiO₆ triangle, show that there is no compositional gap between diopside and fassaitic pyroxene in metamorphic rocks, and that the fassaitic pyroxene in alkalic rocks becomes richer in both CaAl₂SiO₆ and CaFeAlSiO₅ components as crystallization proceeds. These results agree with those obtained in the experimental study.     

Ag-rich Tetrahedrite in the El Zancudo Deposit,Colombia: Occurrence,Chemical Compositions and Genetic Temperatures

Chemical compositions of tetrahedrite—Ag-rich tetrahedrite—freibergite solid solutions (Ag-rich tetrahedrite_ss) and homogenization temperatures of fluid inclusions in quartz and carbonates of seventeen samples from nine veins in the El Zancudo deposit, Antioquia, Colombia, were investigated to reveal the origin of silver in Ag-rich tetrahedrite_ss, to derive their crystallization temperatures and to examine the relationship between chemical compositions of Ag-rich tetrahedrite_ss and their crystallization temperatures. The ores consist of arsenopyrite, pyrite, sphalerite, Ag-rich tetrahedrite_ss, galena, boulangerite, andorite, owyheeite, diaphorite, jamesonite, miargyrite, bournonite, chalcopyrite, and electrum. Ag-rich tetrahedrite_ss forms about 10 volume % of the total ores and is one of the most common and widely distributed sulfosalts in this deposit. Ag-rich tetrahedrite_ss is rich in Ag (1.13 to 31.02 wt%) and Sb (22.93 to 29.82 wt%), and poor in As (0.06 to 2.43 wt%), consistent with the reported incompatibilities of Ag and As in Ag-rich tetrahedrite_ss. The Zn/(Zn + Fe)-, Ag/(Ag + Cu)- and Sb/(Sb + As + Bi)-atomic ratios exhibit some variations among the veins. Ag-rich tetrahedrite_ss with higher Ag/(Ag + Cu) ratios coexist with diaphorite, whereas those with lower ratios are not associated with this sulfosalt. Ag-rich tetrahedrite_ss in the assemblages of Ag-rich tetrahedrite_ss+ sphalerite and of Ag-rich tetrahedrite_ss+ bournonite + galena shows no Zn ↔ Fe and Cu ↔ Ag variations between core and rim, respectively, negating the possibility of solid state reaction during cooling. Ag-rich tetrahedrite_ss is thus regarded as primary phase. Homogenization temperatures of primary fluid inclusions in quartz and carbonates co-existing with Ag-rich tetrahedrite_ss define the mineralization temperatures of 134 to 263°C. Independent crystallization temperatures of Ag-rich tetrahedrite estimated based on Zn/(Zn + Fe) and Ag/(Ag + Cu) ratios of the Ag-rich tetrahedrite_ss associated with silver minerals such as miargyrite, andorite and diaphorite using Sack's thermochemical database lie in a range between 170 and ∼250°C. Both results are thus in good agreement.     

Mobility-dependent response of aquatic animal species richness to a wetland network in an agricultural landscape

Management of wetland connectivity is important for biodiversity conservation. In the modern agricultural landscape, the natural connections between floodplain wetlands have been greatly altered. Agricultural ditches and channelized streams are widely distributed in floodplains, which may contribute to the maintenance of wetland connectivity and biodiversity. To determine how these watercourse networks affect wetland biodiversity, we examined the relationship between the species richness of aquatic animals and wetland connectivity, with a special focus on species mobility. From July to August 2011, fish and aquatic insects were collected from 24 wetlands in northern Japan. To determine the degree of wetland connectivity, we assessed the relative importance of individual wetlands in maintaining the entire wetland network using two connectivity indices: hydrologic connectivity via watercourses and spatial connectivity defined as Euclidian distances between wetlands using graph theory. We found that only high mobility groups of both taxa could enhance species richness in either a hydrologic (fish) or spatial (insect) wetland network. The species richness of insects with high-flying ability was found to increase as spatial connectivity increased. Furthermore, the species richness of fish with high-swimming ability was positively influenced by hydrologic connectivity, most likely because highly mobile species were able to reach suitable habitats and migrate from source populations in a wetland network owing to their good mobility. Our findings indicate that hydrologic network is important for maintaining biodiversity as well as spatial connectivity. It is important to focus conservation efforts on key wetlands with high hydrologic and spatial connectivity in future wetland management.     

Ore and Skarn Mineralogy of the Yamato Mine,Yamaguchi Prefecture,Japan, with Emphasis on Silver‐, Bismuth‐, Cobalt‐, and Tin‐bearing Sulfides

Assemblages and chemical compositions of ore minerals from the Yamato mine, Yamaguchi Prefecture, Japan, were investigated in detail to clarify its characteristics as a skarn deposit. Special attention was paid to silver‐, bismuth‐, cobalt‐, and tin‐bearing sulfide minerals and native gold at the mine, which are described here for the first time. Samples of arsenopyrite‐dominant massive ore, and garnet‐rich, clinopyroxene‐garnet‐rich, and wollastonite‐bearing skarn ores were collected from the mine dump. Arsenopyrite is the most abundant ore mineral (>80 vol.%) in the massive ore, in association with both As‐poor/free and As‐bearing pyrite. The major ore minerals in the skarn specimens are pyrite, pyrrhotite, arsenopyrite, chalcopyrite, galena, and sphalerite, along with minor argentite, Ag‐Pb‐Bi sulfate, matildite, bismuthinite, native bismuth, molybdenite, scheelite, stannite, stannoidite, cassiterite, cobaltite, gersdorffite, and Co‐rich violarite. In addition, native gold is observed in the interstices of gangue minerals. Based on the mineral assemblages and textures of the specimens examined, the major ore minerals formed in the early stage of mineralization, and the Bi‐, Ag‐, Co‐, Ni‐, As‐ and Sn‐mineralization occurred in the middle stage. Native gold was deposited in the late stage. The estimated formation temperature of the middle mineralization stage was 312±5 °C, according to iron and zinc partitioning between stannite and coexisting sphalerite. The mineralogical properties and mineralization process of the Yamato mine are consistent with those of common skarn‐ and vein‐type ore deposits associated with ilmenite‐series granitoids in the San‐yo and San‐in districts.     

The Wide Band Spectrometer on the SOLAR-A

The SOLAR-A spacecraft has spectroscopic capabilities in a wide energy band from soft X-rays to gamma-rays. The Wide Band Spectrometer (WBS), consisting of three kinds of spectrometers, soft X-ray spectrometer (SXS), hard X-ray spectrometer (HXS) and gamma-ray spectrometer (GRS), is installed on SOLAR-A to investigate plasma heating, high-energy particle acceleration, and interaction processes. SXS has two proportional counters and each counter provides 128-channel pulse height data in the 2–30 keV range every 2 s and 2-channel pulse count data every 0.25 s. HXS has a NaI scintillation detector and provides 32-channel pulse height data in the 20–400 keV range every 1 s and 2-channel pulse count data every 0.125 s. GRS has two identical BGO scintillation detectors and each detector provides 128-channel pulse height data in the 0.2–10 MeV range every 4 s and 4-channel pulse count data (0.2–0.7, 0.7–4, 4–7, and 7–10 MeV) every 0.25–0.5 s. In addition, each of the BGO scintillation detectors provides 16-channel pulse height data in the 8–100 MeV range every 4 s and 2-channel pulse count data (8–30 and 30–100 MeV) every 0.5 s. The SXS observations enable one to study the thermal evolution of flare plasma by obtaining time series of electron temperatures and emission measures of hot plasma; the HXS observations enable one to study the electron acceleration and heating mechanisms by obtaining time series of the electron spectrum; and the GRS observations enable one to study the high-energy electron and ion acceleration and interaction processes by obtaining time series of electron and ion spectra.After the launch the name of SOLAR-A has been changed to YOHKOH.     

Ti-rich hydroandradites from the Sanbagawa metamorphic rocks of the Shibukawa area,central Japan

Ti-rich hydroandradite often occurs, though usually as a minor constituent, in serpentinized ultramafic rocks and associated gabbroic rocks of the Sanbagawa metamorphic belt. The chemistry of the host rocks is commonly characterized by undersaturation with SiO₂. Two Ti-rich hydroandradites from metasomatized gabbroic rocks of the Shibukawa area have been chemically analysed by the wet method. Mössbauer experiments indicate the presence of Fe³⁺ and Fe²⁺ in the octahedral sites of these Ti-rich hydroandradites. Wet chemical analyses for total reducing capacity of the present garnets by two different methods together with Mössbauer data imply the presence of octahedral Ti³⁺ in their structure. Ti-rich hydroandratites, apart from their hydrous property, have a similar crystal chemistry to natural Ti-rich andradites. Ti-rich hydroandradites were probably formed in rocks with unusual chemical compositions within a P-T region of 300–400° C and 4–7 kb under limited conditions of relatively low oxygen fugacity and low μCO₂.     

Gold Mineralization of the Gatsuurt Deposit in the North Khentei Gold Belt,Central Northern Mongolia

Mineral assemblages, chemical compositions of ore minerals, wall rock alteration and fluid inclusions of the Gatsuurt gold deposit in the North Khentei gold belt of Mongolia were investigated to characterize the gold mineralization, and to clarify the genetic processes of the ore minerals. The gold mineralization of the deposit occurs in separate Central and Main zones, and is characterized by three ore types: (i) low‐grade disseminated and stockwork ores; (ii) moderate‐grade quartz vein ores; and (iii) high‐grade silicified ores, with average Au contents of approximately 1, 3 and 5 g t^?1 Au, respectively. The Au‐rich quartz vein and silicified ore mineralization is surrounded by, or is included within, the disseminated and stockwork Au‐mineralization region. The main ore minerals are pyrite (pyrite‐I and pyrite‐II) and arsenopyrite (arsenopyrite‐I and arsenopyrite‐II). Moderate amounts of galena, tetrahedrite‐tennantite, sphalerite and chalcopyrite, and minor jamesonite, bournonite, boulangerite, geocronite, scheelite, geerite, native gold and zircon are associated. Abundances and grain sizes of the ore minerals are variable in ores with different host rocks. Small grains of native gold occur as fillings or at grain boundaries of pyrite, arsenopyrite, sphalerite, galena and tetrahedrite in the disseminated and stockwork ores and silicified ores, whereas visible native gold of variable size occurs in the quartz vein ores. The ore mineralization is associated with sericitic and siliceous alteration. The disseminated and stockwork mineralization is composed of four distinct stages characterized by crystallization of (i) pyrite‐I + arsenopyrite‐I, (ii) pyrite‐II + arsenopyrite‐II, (iii) galena + tetrahedrite + sphalerite + chalcopyrite + jamesonite + bournonite + scheelite, and iv) boulangerite + native gold, respectively. In the quartz vein ores, four crystallization stages are also recognized: (i) pyrite‐I, (ii) pyrite‐II + arsenopyrite + galena + Ag‐rich tetrahedrite‐tennantite + sphalerite + chalcopyrite + bournonite, (iii) geocronite + geerite + native gold, and (iv) native gold. Two mineralization stages in the silicified ores are characterized by (i) pyrite + arsenopyrite + tetrahedrite + chalcopyrite, and (ii) galena + sphalerite + native gold. Quartz in the disseminated and stockwork ores of the Main zone contains CO₂‐rich, halite‐bearing aqueous fluid inclusions with homogenization temperatures ranging from 194 to 327°C, whereas quartz in the disseminated and stockwork ores of the Central zone contains CO₂‐rich and aqueous fluid inclusions with homogenization temperatures ranging from 254 to 355°C. The textures of the ores, the mineral assemblages present, the mineralization sequences and the fluid inclusion data are consistent with orogenic classification for the Gatsuurt deposit.     

The Crater Mountain Deposit,Papua New Guinea: Porphyry‐related Au–Te System

Ore mineralization and wall rock alteration of Crater Mountain gold deposit, Papua New Guinea, were investigated using ore and host rock samples from drill holes for ore and alteration mineralogical study. The host rocks of the deposit are quartz‐feldspar porphyry, feldspar‐hornblende porphyry, andesitic volcanics and pyroclastics, and basaltic‐andesitic tuff. The main ore minerals are pyrite, sphalerite, galena, chalcopyrite and moderate amounts of tetrahedrite, tennantite, pyrrhotite, bornite and enargite. Small amounts of enargite, tetradymite, altaite, heyrovskyite, bismuthinite, bornite, idaite, cubanite, native gold, CuPbS₂, an unidentified Bi‐Te‐S mineral and argentopyrite occur as inclusions mainly in pyrite veins and grains. Native gold occurs significantly in the As‐rich pyrite veins in volcanic units, and coexists with Bi‐Te‐S mineral species and rarely with chalcopyrite and cubanite relics. Four mineralization stages were recognized based on the observations of ore textures. Stage I is characterized by quartz‐sericite‐calcite alteration with trace pyrite and chalcopyrite in the monomict diatreme breccias; Stage II is defined by the crystallization of pyrite and by weak quartz‐chlorite‐sericite‐calcite alteration; Stage III is a major ore formation episode where sulfides deposited as disseminated grains and veins that host native gold, and is divided into three sub‐stages; Stage IV is characterized by predominant carbonitization. Gold mineralization occurred in the sub‐stages 2 and 3 in Stage III. The fS₂ is considered to have decreased from ～10^?2 to 10^?14 atm with decreasing temperature of fluid.