DISTRIBUTION OF AEROSOL EXTINCTION IN THE LOWER TROPOSPHERE BY MICRO-PULSE LIDAR OBSERVATION

The profiles of aerosol extinction coefficients are investigated by micro-pulse lidar(MPL)combined with the meteorological data in the lower troposphere at Meteorological ResearchInstitute(MRI).Japan.Larger extinction values of aerosol are demonstrated in the nocturnalstable air layer with larger Richardson number,and light wind velocities are favorable for aerosolconcentrating in the planetary boundary layer(PBL).But aerosol extinction coefficients showlarger values over the altitudes of 2.0 to 5.0km where correspond to higher relative humidity(RH).The tops of PBL identified by the aerosol extinction profiles almost agree with ones byradiosonde data.The diurnal variations of aerosol extinction profiles are clearly displayed,intensive aerosol layers usually are formed over the period of mid-morning to 1400 Loeal Time(LT).then elapse in the cloudless late afternoon and nighttime.Thermal eonvection or turbulenttransport from the surfaee probably dominates these temporal and spatial changes of aerosoldistribution.     

A multi‐geochronological study of the Hakusan volcano,central Japan

The Hakusan volcano, central Japan, is located in a region where two subducting plates (the Pacific Plate and the Philippine Sea Plate) overlap near the junction of four plates adjacent to the Japanese Islands (the Pacific Plate, the Philippine Sea Plate, the Eurasia Plate, and the North American Plate). The Hakusan volcano consists of products from four major volcanic episodes: Kagamuro, Ko‐hakusan, and Shin‐Hakusan I and II. To date the eruption events of the Hakusan volcano we applied thermoluminescence and fission track methods. ²³⁸U(²³⁴U)–²³⁰Th disequilibrium and ²⁰⁶Pb/²³⁸U methods were applied to date the zircon crystallization ages for estimating the magma residence time before the eruptions. The eruption ages we obtained are ca 250 ka for Kagamuro, ca 100 ka and ca 60 ka for Ko‐Hakusan, ca 50 ka for Shin‐Hakusan I, and <10 ka for Shin‐Hakusan II. They are concordant with previous reports based on K–Ar dating. Some of the pyroclastic rocks, possibly originating from Shin‐Hakusan II activities, are dated to be ca 36 ka or 50 ka, and belong to the Shin‐Hakusan I activity. The zircon crystallization ages show several clusters prior to eruption. The magma residence time was estimated for each volcanic activity by comparing the major crystallization events and eruption ages, and we found a gradual decrease from ca. 500 ky for the Kagamuro activity to ca. 5 ky for the Shin‐Hakusan II activity. This decrease in residence time may be responsible for the decrease in volume of erupted material estimated from the current topography of the region. The scale of volcanic activity, which was deduced from the number of crystallized zircons, is more or less constant throughout the Hakusan volcanic activity. Therefore, the decrease in magma residence time is most likely the result of stress field change.     

Tidal switch on metabolic activity: Salinity induced responses on bacterioplankton metabolic capabilities in a tropical estuary

“Biolog” plates were used to study the changes in the metabolic capabilities of bacterioplankton over a complete tidal cycle in a tropical ecosystem (Cochin Estuary) along southwest coast of India. The pattern of utilization of carbon sources showed a definite shift in the community metabolism along a salinity gradient. Multivariate statistical analysis revealed two communities, namely allochthonous bacterioplankton sensitive to salinity and autochthonous bacterioplankton, which are tolerant to wide salinity fluctuations. Regression analysis showed salinity as the most important parameter influencing the physiological profile of bacterioplankton, irrespective of tide. Apart from salinity, limno-tolerant retrievable counts and halo-tolerant retrievable counts also accounted for the metabolic variation of bacterioplankton during low and high tides, respectively. The shift in the substrate utilization from carbohydrates to amino acids appears to be due to the physiological adaptation or nitrogen limitation of bacterial community with increasing salinity.     

Mantle hornblendites of Naein ophiolite (Central Iran): Evidence of deep high temperature hydrothermal metasomatism in an upper mantle section

The Naein ophiolite is the most complete ophiolitic exposure in Cental Iran and considered as a remnant of the Mesozoic Central East Iranian microcontinent (CEIM) confining oceanic crust. In the northeastern part of this ophiolite (Darreh Deh area) within the mantle peridotites, a few hundred meters below the top of the Moho transition zone (MTZ), the hornblendites are present as dykes (former cracks and joints) from a few millimeters to nearly 50 cm wide. They have sharp boundaries with the surrounding mantle harzburgites and dunites. These hornblendites are pale green and coarse-grained in hand specimen and composed of magnesio-hornblende (Mg# = 0.93), chlorite (penninite and clinochlore, Mg# = 0.95), Cr-spinel (chromite, Cr# = 0.67 and Mg# = 0.55), tremolite, calcite and dolomite. Tremolites were formed by retrograde metamorphism of hornblendes. Calcite and dolomite occur as late-stage veins. Very high amount of primary hydrous phases (~94 vol % hornblende and chlorite), as well as peculiar mineralogical and chemical characteristics of the Naein ophiolite mantle hornblendites, do not match a magmatic origin. They are possibly products of the reaction between mantle peridotites and seawater-originated supercritical fluids, rich in silicate components. The presence of primary hydrous phases (hornblende and chlorite) may reveal high activity of H₂O in the involved solution. The chemical composition of chromite in the hornblendites is near to the average chromite composition from the surrounding harzburgite and dunite. This suggests that the main source of Cr should be chromites of nearby peridotites, which were totally or partly dissolved by hydrothermal fluids. The positive anomaly of Eu in the chondrite-normalized REE patterns of hornblendes, high modal abundance of Ca-rich hornblende, as well as presence of calcite and dolomite, point to seawater ingression through the gabbros in to the uppermost mantle peridotites. The higher value of MgO than CaO, presence of high-Cr chromite and Cr-enrichment of hornblendes and chlorites indicate a higher contribution of peridotites rather than gabbros to the chemical characteristics of the involved fluids. This study shows that circulation of possibly seawater-derived high temperature hydrous fluids in the upper mantle can leach and provide necessary elements to form hornblendite in joints and cracks of the uppermost mantle.     

Occurrence and chemical composition of amphiboles and related minerals in corundum-bearing mafic rock from the Horoman Peridotite Complex, Japan

A corundum-bearing mafic rock in the Horoman Peridotite Complex, Japan, was derived from upper mantle conditions to lower crustal conditions with surrounding peridotites. The amphiboles found in the rock are classified into 3 types: (1) as interstitial and/or poikilitic grains (Green amphibole), (2) as a constituent mineral of symplectitic mineral aggregates with aluminous spinel at grain boundary between olivine and plagioclase (Symplectite amphibole) and (3) as film-shaped thin grains, usually less than 10 μm in width, at grain boundary between olivine and clinopyroxene (Film-shaped amphibole). The Film-shaped amphibole is rarely associated with orthopyroxene extremely low in Al₂O₃, Cr₂O₃ and CaO (Low-Al OPX). These minerals were formed by infiltration of SiO₂- and volatile-rich fluids along grain boundaries after the rock was recrystallized at olivine-plagioclase stability conditions, i.e. the late stage of the exhumation of the Horoman Complex.

Chondrite-normalized rare earth element patterns and primitive mantle-normalized trace-element patterns of the Green amphibole and clinopyroxene are characterized by LREE-depleted patterns with Eu positive and negative anomalies of Zr and Hf. These geochemical characteristics of the constituent minerals were inherited from original whole-rock compositions through a reaction involving both pre-existing clinopyroxene and plagioclase. We propose that the fluids were originally rich in a SiO₂ component but depleted in trace-elements. Dehydration of the surrounding metamorphic rocks in the Hidaka metamorphic belt, probably related to intrusion of hot peridotite body into the Hidaka crust, is a plausible origin for the fluids.     

Formation and compositional variation of phlogopites in the Horoman peridotite complex,Hokkaido, northern Japan: implications for origin and fractionation of metasomatic fluids in the upper mantle

Harzburgite and lherzolite tectonites from the Horoman peridotite complex, Hokkaido, northern Japan, contain variable amounts of secondary phlogopite and amphibole. Phlogopite-rich veinlets parallel to the foliation planes usually cut olivine-rich parts of the rocks; single-grained interstitial phlogopites are usually associated with orthopyroxene grains. Amphiboles are disseminated in rocks or sometimes occur in the phlogopite-rich veinlets. Within individual veinlets, phlogopites show extensive inter-grain variations in K/(K + Na) ratio (0.96–0.75), generally decreasing from the central (usually the thickest) part towards the marginal parts of veinlets. In contrast, Ti contents are nearly constant in Ti-poor veins or decrease slightly with decreasing K/(K + Na) in T-rich veins. Variation of Ti in phlogopites is very large (0.1–6.8 wt%) and is inversely correlated with Mg/(Mg + Fe^*) (Fe^*, total iron) atomic ratios, which vary from 0.96 to 0.88. Intra-vein variation of phlogopite chemistry (especially K/(K + Na) ratio) could be achieved by in situ fractional crystallization of trapped fluids; variation of Ti, however, cannot be explained by in situ fractionation of the fluids, indicating various Ti contents of the parent fluids. It is suggested that fluids responsible for the formation of the Horoman phlogopites and amphiboles were magmatic volatiles successively released from evolving alkali basaltic magmas. Individual fluids trapped within peridotites were fractionated, precipitating phlogopites successively poorer in K. When the fluids became rich enough in Na, amphiboles co-precipitated with phlogopites. Similar fractional crystallization of phlogopites and amphiboles is expected in the upper mantle on a larger scale if fluids move upwards. This process may control, at least partly, a lateral K/Na distribution in the upper mantle; K and Na may be concentrated in deeper and shallower parts, respectively.     

DISTRIBUTION OF AEROSOL EXTINCTION IN THE LOWER TROPOSPHERE BY MICRO-PULSE LIDAR OBSERVATION*

The profiles of aerosol extinction coefficients are investigated by micro-pulse lidar(MPL) combined with the meteorological data in the lower troposphere at Meteorological Research Institute(MRI).Japan.Larger extinction values of aerosol are demonstrated in the nocturnal stable air layer with larger Richardson number,and light wind velocities are favorable for aerosol concentrating in the planetary boundary layer(PBL).But aerosol extinction coefficients show larger values over the altitudes of 2.0 to 5.0km where correspond to higher relative humidity(RH).The tops of PBL identified by the aerosol extinction profiles almost agree with ones by radiosonde data.The diurnal variations of aerosol extinction profiles are clearly displayed,intensive aerosol layers usually are formed over the period of mid-morning to 1400 Loeal Time(LT).then elapse in the cloudless late afternoon and nighttime.Thermal eonvection or turbulent transport from the surfaee probably dominates these temporal and spatial changes of aerosol distribution.     

Crustal anorthosite formation by deep-seated hydrothermal circulation beneath fast-spreading axis: Constraints from chronological approach,Sr isotope,and fluid–chromite inclusion investigation

Hydrothermal circulation beneath the spreading axis plays a significant role in the exchange of energy and mass between the solid Earth and the oceans. Deep-seated hydrothermal circulation down to the crust/mantle boundary in the fast-spreading axis has been introduced by a number of studies regarding geological investigations and numerical models. In order to assess a reaction between hydrothermal fluid and host rock around the crust/mantle boundary, we conducted bulk trace element and Sr isotope analyses with a series of in situ investigations for crustal anorthosite, a reaction product between hydrothermal fluid and gabbro in the lowermost crustal section along Wadi Fizh, northern Oman ophiolite. In addition, we conducted titanite U–Pb isotope analyses to evaluate timing of the crustal anorthosite formation in the framework of the evolutional process of the Oman ophiolite. We estimated the formation age of the crustal anorthosite at 97.5 Ma ± 5.0 Ma, overlapping with the timing of the crust formation in the paleo spreading axis. The crustal anorthosite shows high-Th/U ratio (~2.5) and high-initial ⁸⁷Sr/⁸⁶Sr ratio (0.7050) due to seawater-derived hydrothermal fluid ingress into the precursor gabbro. With using analytical technique of micro-excavation at cryo-temperature, we detected Cl from a few micrometer-sized inclusion of aqueous fluid and chromite grains. The solubility of Cr was enhanced by complexation reactions with Cl in the hydrothermal fluid. Regarding reconstructed three-dimensional mass distribution of the inclusion and chromite composition, maximum Cr content of parental fluid was estimated at ~69 000 μg/g. The exceptionally high-Cr content was achieved locally by leaking of fluid and synchronous chromite crystallization during fluid entrapment. Presence of the deep-seated hydrothermal circulation could be assigned to the segment end, where cold seawater penetrates into the lowermost crust and extract heat along widely spaced network-like fluid channel.     

Did boninite originate from the heterogeneous mantle with recycled ancient slab?

Boninites are widely distributed along the western margin of the Pacific Plate extruded during the incipient stage of the subduction zone development in the early Paleogene period. This paper discusses the genetic relationships of boninite and antecedent protoarc basalt magmas and demonstrates their recycled ancient slab origin based on the T–P conditions and Pb–Hf–Nd–Os isotopic modeling. Primitive melt inclusions in chrome spinel from Ogasawara and Guam islands show severely depleted high‐SiO₂, MgO (high‐silica) and less depleted low‐SiO₂, MgO (low‐silica and ultralow‐silica) boninitic compositions. The genetic conditions of 1 346 °C at 0.58 GPa and 1 292 °C at 0.69 GPa for the low‐ and ultralow‐silica boninite magmas lie on adiabatic melting paths of depleted mid‐ocean ridge basalt mantle with a potential temperature of 1 430 °C in Ogasawara and of 1 370 °C in Guam, respectively. This is consistent with the model that the low‐ and ultralow‐silica boninites were produced by remelting of the residue of the protoarc basalt during the forearc spreading immediately following the subduction initiation. In contrast, the genetic conditions of 1 428 °C and 0.96 GPa for the high‐silica boninite magma is reconciled with the ascent of more depleted harzburgitic source which pre‐existed below the Izu–Ogasawara–Mariana forearc region before the subduction started. Mixing calculations based on the Pb–Nd–Hf isotopic data for the Mariana protoarc basalt and boninites support the above remelting model for the (ultra)low‐silica boninite and the discrete harzburgite source for the high‐silica boninite. Yb–Os isotopic modeling of the high‐Si boninite source indicates 18–30 wt% melting of the primitive upper mantle at 1.5–1.7 Ga, whereas the source mantle of the protoarc basalt, the residue of which became the source of the (ultra)low‐Si boninite, experienced only 3.5–4.0 wt% melt depletion at 3.6–3.1 Ga, much earlier than the average depleted mid‐ocean ridge basalt mantle with similar degrees of melt depletion at 2.6–2.2 Ga.