A new type of orthopyroxenite xenolith from Takashima, Southwest Japan: silica enrichment of the mantle by evolved alkali basalt

We found fine-grained Fe-rich orthopyroxene-rich xenoliths (mainly orthopyroxenite) containing partially digested dunite fragments of Group I from Takashima, Southwest Japan. Orthopyroxenite veinlets, some of which contain plagioclase at the center, also replace olivine in dunite and wehrlite xenoliths of Group I. This shows high reactivity with respect to olivine of the melt involved in orthopyroxenite formation, indicating its high SiO₂ activity. The secondary orthopyroxene of this type is characterized by low Mg# [= Mg/(Mg + total Fe) atomic ratio] (down to 0.73) and high Al₂O₃ contents (5–6 wt%). It is different in chemistry from other secondary orthopyroxenes found in peridotite xenoliths derived from the mantle wedge. Clinopyroxenes in the Fe-rich orthopyroxenite show a convex-upward REE pattern with a crest around Sm. This pattern is strikingly similar to that of clinopyroxenes of Group II pyroxenite xenoliths and of phenocrystal and xenocrystal clinopyroxenes, indicating involvement of similar alkali basaltic melts. The Fe-rich orthopyroxenite xenoliths from Takashima formed by reaction between evolved alkali basalt melt and mantle olivine; alkali basalt initially slightly undersaturated in silica might have evolved to silica-oversaturated compositions by fractional crystallization at high-pressure conditions. The Fe-rich orthopyroxenites occur as dikes within the uppermost mantle composed of dunite and wehrlite overlying pockets of Group II pyroxenites. The orthopyroxene-rich pyroxenites of this type are possibly common in the uppermost mantle beneath continental rift zones where alkali basalt magmas have been prevalent.     

Jadeite, albite and nepheline as inclusions in spinel of chromitite from Hess Deep, equatorial Pacific: their genesis and implications for serpentinite diapir formation

Polymineralic inclusions which consist of a few grains of diopside, enstatite, jadeite, nepheline, albite, pargasite, phlogopites and olivine were found in chromian spinel in a chromitite pod and in troctolite from Hess Deep, equatorial Pacific. The inclusion mineral suite in chromitite is characterized by Na-Al silicates, such as jadeite, nepheline and albite. Jadeite and nepheline commonly coexist with enstatite, and tend to occur as interstitial grains between subhedral enstatite (or other minerals) and host spinel. Albite, diopside and enstatite occur as equant inclusions. The mafic minerals in the inclusions have similar chemistry to those found in the troctolite and dunite. The modes of occurrence and mineral chemistry of the inclusions are controlled by magmatic precipitation, and subsequent reequilibration due to decrease of temperature in the uppermost mantle. The mafic minerals in spinel inclusions were crystallized from a melt enriched in Cr and some incompatible components formed by melt-mantle interaction process mixed to various extent with subsequently supplied more primary melt. Albite and nepheline could also be formed at the magmatic stage. Jadeite was formed by a subsolidus reaction of albite and nepheline at low temperatures (250–300 °C) at slightly less than 3 kbar. This requires a remarkable temperature decrease, at least locally, of the uppermost mantle and crust. The Hess Deep rocks were formed in the uppermost mantle beneath a spreading-ridge axis at more than 1000 °C, and were transposed outwards from the axis by corner flow. At the off-ridge conditions, the rocks were cooled and serpentinized by circulation of sea water at the mantle depth to form jadeite in chromitite. The serpentinized portion could have risen as a kind of serpentinite diapir through the thin crust up to the ocean floor. Received: 24 January 1997 / Accepted: 6 November 1997     

Ore value-tonnage diagrams for resource assessment

An ore value-tonnage diagram has been proposed for assessing mineral resources. Diagrams of W+Mo, and Pb+Zn deposits show a good linearity between ore value and logarithms of cumulative ore tonnage. Diagrams of the massive sulfide, orthomagmatic, placer, porphyry, replacement, and stratabound types are also linear. It is assumed, therefore, that deposits of each of these commodities and these types belong to a single population. In contrast, the ore value-tonnage relations of all the deposits analyzed here is approximated by the combination of two exponential functions. The same feature is seen for deposits of the Cu+W+Mo, Cu+Pb+Zn, and Au+Ag commodities, and of the vein and unconformity-related types. This suggests that deposits belonging to each of such categories are divided into the high and low value groups. We can expect, accordingly, to find high value deposits of such categories.     

Observational aspects on a dominant spectral frequency in an airflow over a weeping-lovegrass stand

Mean and fluctuating wind velocities were measured above a flexible stand (weeping-lovegrass). A waving phenomenon Honami appeared over the stand during the observation period. Some spectral parameters were derived from the vertical wind fluctuations. A dependency of frequency on mean horizontal wind velocity was found. The result, n _m = 0.66u, was obtained under the range of wind speeds from 0.9 m s^-1 to 3.1 m s^-1 just above the canopy.     

Stability of pentlandite in the Fe-Ni-Co-S system

Pentlandite has a wide compositional range in the Fe-Ni-Co-S system and the Fe-Ni-S system. The metal : sulfur atomic ratio is approximately 9 : 8. The Co content of pentlandite from the Kamaishi ore deposit and one from the Outokumpu ore deposit (Knop et al. 1965) varies from a Co-free to nearly a Co₉S₈ composition. Pentlandite forms a complete solid solution between (Fe, Ni)_9±x S₈ and Co_9±x S₈ in the 600°–300°C temperature range. On the other hand, it is presumed that the pentlandite solid solution decomposes into two fields toward the (Fe, Ni)₉S₈ and Co₉S₈ members at 200°C. The field of solid solution at 500°C is the most extensive and includes all of the other solid-solution fields. The metal : sulfur ratio of the solid solution varies systematically, i.e., the Fe-rich field sinks toward the Fe-Ni-Co plane away from the M₉S₈ section, and contrarily the Ni-rich field shifts toward the sulfur apex. The d ₀₄₄ value decreases with increasing S, Ni, or Co contents in pentlandite. The Kamaishi pentlandites, Iwate Prefecture, Japan, lie within or close to the solid-solution field at 300°C, showing a very good correlation with the Co : Ni ratio of the homogeneous natural pyrrhotite phase.     

Discharge of H2 from the Atotsugawa and Ushikubi Faults,Japan, and its relation to earthquakes

The concentration of H₂ in soil gases has been measured weekly at five stations on the Atotsugawa and Ushikubi faults in northern central Main Island, Japan, since 1981 in search of possible relationship with earthquakes. The observed H₂ concentration varies from lower than 1 ppm to 7.8% in time and place. When a large earthquake (M: 7.7, epicenter distance: 486 km) occurred on 26 May 1983, an outstanding discharge of H₂ was observed at all five stations, preseismically at three of them, and coseismically at the other two. Simultaneous H₂ emission was also observed at some stations in seven other occasions. These periods of unusual H₂ discharge nearly coincided with occurrences of major earthquakes in Japan, but not of local minor earthquakes along the Atotsugawa fault. This fault, being a deep fracture zone, may be sensitive to large-scale crustal stress changes which incidentally cause the major earthquakes. Increased H₂ may be produced by rock fracture caused by the increased stresses on the fault and by the earthquakes themselves. Local minor earthquakes along Atotsugawa fault with magnitude lower than 3 may be unable to cause sufficient rock fracture to produce significant H₂.     

Role of Stress-controlled Flow Pathways in HDR Geothermal Reservoirs

— We addressed effects of in situ stress on the formation of flow pathways in fractured rocks in geothermal reservoirs, especially for HDR projects. Here we focused on fractures which are critically-stressed, causing shear slip in a current stress field. The sliding is likely to break sealing in the fractures and, as a result, to increase their permeability. Such a mechanism is possibly significant under high-temperature conditions at geothermal fields because of temperature enhancement on chemical reactions for the sealing. We present a procedure to estimate the orientation of the critically-stressed fractures relative to axes of in situ principal stress with the aid of the Mohr diagram. The procedure allows us to evaluate intuitively how the orientation changes with factors such as magnitude of in situ principal stresses and pore pressure. We applied the procedure to estimate possible orientations of the critically-stressed fractures in major HDR test sites. Results show that overall alignments of microseismicity during hydraulic stimulation are within predicted ranges for possible orientations of the critically-stressed fractures. Furthermore, it was found that if the state of in situ stress is not favorable to cause sliding of natural fractures, it tends to lead a high wellhead pressure at hydraulic stimulation and a high recovery rate at circulation. On the other hand, if the state of in situ stress is favorable for sliding, it tends vice versa to lead a low wellhead pressure at hydraulic stimulation and a low recovery rate at circulation.     

Mineral Paragenesis and Fluid Inclusions of Some Pluton-hosted Vein-type Copper Deposits in the Coastal Cordillera, Northern Chile

Abstract. Formation conditions of some vein-type copper deposits of the Tocopilla district (Deseada, San Jose, Santa Rosa) and the Gatico district (Yohanita, Toldo-Velarde, Argentina) in the Coastal Cordillera of northern Chile were inferred from mineral paragenesis and fluid inclusion data, and were compared with those of neighboring stratiform copper deposits. The vein-type copper deposits are hosted in Late Jurassic dioritic to quartz-dioritic plutons intruding extensively an andesite-dominant volcanic pile of the Jurassic La Negra Formation. Primary mineralization is characterized by chalcopyrite + magnetite + pyrite + bornite, and supergene alteration of these minerals produced anilite, covellite, atacamite and chrysocolla. The hypogene mineral assemblage indicates relatively high sulfur fugacity and weakly oxidized conditions, distinct from the stratiform copper deposits formed under low sulfur fugacity and moderately oxidized conditions. Furthermore, the fluid inclusion data of the vein-type deposits indicate high temperature (401–560C) and high salinity (39–68 wt% NaCl equiv.) ranges in contrast to the stratiform deposits, suggesting that this type of deposits formed by magma-associated hypersaline ore fluids.     

Closed-system geochemical recycling of crustal materials in alpine-type peridotite

We examined aluminous mafic rock (with or without corundum or sapphirine) alternating with peridotite from the Ronda peridotite massif, southern Spain. On the basis of petrographic characteristics, these mafic rocks show a decompression history from high pressure (P > 1.5 GPa), but on the basis of their geochemical characteristics, they are crystal accumulates of plagioclase, clinopyroxene, and olivine formed within the lower crust (P < 1 GPa). A complex evolution history, including higher-pressure recrystallization after initial formation as cumulate gabbros at lower-pressure conditions, is proposed. The aluminous mafic rocks and their peridotite hosts are inferred to be recycled crustal materials now observed as centimeter-scale layered components in alpine-type peridotite. The rocks retained their original cumulate compositions; that is, their compositions were not affected by melting and metasomatic modifications during subduction, intense deformation within the upper mantle, and upwelling to the surface.