Polarization Calibration of the <Emphasis Type="Italic">Chromospheric Lyman-Alpha SpectroPolarimeter</Emphasis> for a 0.1% Polarization Sensitivity in the VUV Range. Part II: In-Flight Calibration

The Chromospheric Lyman-Alpha SpectroPolarimeter is a sounding rocket instrument designed to measure for the first time the linear polarization of the hydrogen Lyman-\({\upalpha }\) line (121.6 nm). The instrument was successfully launched on 3 September 2015 and observations were conducted at the solar disc center and close to the limb during the five-minutes flight. In this article, the disc center observations are used to provide an in-flight calibration of the instrument spurious polarization. The derived in-flight spurious polarization is consistent with the spurious polarization levels determined during the pre-flight calibration and a statistical analysis of the polarization fluctuations from solar origin is conducted to ensure a 0.014% precision on the spurious polarization. The combination of the pre-flight and the in-flight polarization calibrations provides a complete picture of the instrument response matrix, and a proper error transfer method is used to confirm the achieved polarization accuracy. As a result, the unprecedented 0.1% polarization accuracy of the instrument in the vacuum ultraviolet is ensured by the polarization calibration.     

Surface current and vertical thermal structure on the continental slope in Tosa Bay

In order to specify a vertical thermal structure related to surface current variation on the continental slope in Tosa Bay, Japan, we analyzed monthly regular hydrographic measurements in the years 1991–2004. Subsurface temperature below 200 m on the slope was found to vary synchronously with the vertical displacement of the main thermocline around 200 m. It is shown that the vertical-averaged temperature below 200 m is significantly correlated with an along-isobath/southwestward surface current velocity on the slope. This correlation indicates that when a strong (weak) southwestward surface current is observed, temperature below 200 m decreases (increases) simultaneously, that is, isotherms below the 200 m are displaced upward (downward) together with the main thermocline. Moreover, when the strong southwestward flow is detected, across-isobath isotherms around 200 m slope upward toward the offshore direction. Furthermore, it is suggested that as the Kuroshio axis moves offshore south of the bay, the southwestward flow tends to be weakened by the combined effect of other Kuroshio parameters such as transport and stream width as well as the Kuroshio axis position. As a result, it is inferred that the correlation between the surface current and subsurface temperature can be interpreted in terms of the formation and decay of an anticlockwise circulation interacting with a cold eddy.     

Analysis of dust events in 2008 and 2009 using the lidar network, surface observations and the CFORS model

The Asian dust events in 2008 (May 24–June 4 in 2008) and in 2009 (March 12–25, October 13–26, and December 15–28 in 2009) were analyzed with the lidar network observations, surface observations in China, Korea, Japan, and Mongolia, and with the chemical transport model CFORS. Transport of Asian dust and mixing of dust with air pollution aerosols were studied. The event of May 24 to June 4 in 2008 was a significant event unusually late in the spring dust season. The dust event of March 12–25, 2009 was an interesting example of elevated dust layer, and transport of dust from the elevated dust layer to the ground by the boundary layer activity was observed with the lidars and surface observations in Japan. The concentration of air pollution aerosols was relatively high during the dust event, and the results suggest that vertical structure as well as transport path is important for the mixing of dust and air pollution aerosols. The dust events in October and December 2009 were examples of dust events in autumn and winter. The online mode CFORS reproduced the observation data generally well, except for the event of May 24 to June 4 in 2008. The results of the fourdimensional variational assimilation of the lidar network data reproduced the dust concentration in Korea and Japan reasonably in that event.     

Reaction between slab-derived melts and peridotite in the mantle wedge: experimental constraints at 3.8 GPa

Laboratory experiments on natural, hydrous basalts at 1–4 GPa constrain the composition of “unadulterated” partial melts of eclogitized oceanic crust within downgoing lithospheric slabs in subduction zones. We complement the “slab melting” experiments with another set of experiments in which these same “adakite” melts are allowed to infiltrate and react with an overlying layer of peridotite, simulating melt:rock reaction at the slab–mantle wedge interface. In subduction zones, the effects of reaction between slab-derived, adakite melts and peridotitic mantle conceivably range from hybridization of the melt, to modal or cryptic metasomatism of the sub-arc mantle, depending upon the “effective” melt:rock ratio. In experiments at 3.8 GPa, assimilation of either fertile or depleted peridotite by slab melts at a melt:rock ratio 2:1 produces Mg-rich, high-silica liquids in reactions which form pyrope-rich garnet and low-Mg# orthopyroxene, and fully consume olivine. Analysis of both the pristine and hybridized slab melts for a range of trace elements indicates that, although abundances of most trace elements in the melt increase during assimilation (because melt is consumed), trace element ratios remain relatively constant. In their compositional range, the experimental liquids closely resemble adakite lavas in island-arc and continental margin settings, and adakite veins and melt inclusions in metasomatized peridotite xenoliths from the sub-arc mantle. At slightly lower melt:rock ratios (1:1), slab melts are fully consumed, along with peridotitic olivine, in modal metasomatic reactions that form sodic amphibole and high-Mg# orthopyroxene.     

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.     

Mineralogical and geochemical characteristics of hydrothermal alteration of basalt in the Kuroko mine area, Japan: implications for the evolution of a Back Arc Basin hydrothermal system

Basalt in the Furutobe District of the Kuroko mine area in Japan is characterized by abundant chlorite and epidote. Fluid inclusion studies indicate that chlorite is formed at lower temperatures (230–250°C) than epidote (250–280°C). The seawater/basalt mass ratio for the early chlorite-rich alteration was high (max. 40), but that for the later alteration was low (0.1–1.8). The CaO, Na₂O and SiO₂ of the bulk rock correlate negatively with MgO, while FeO and Σ Fe correlate positively with MgO. These changes in the characteristic features of hydrothermal alteration from early to late are generally similar to those for a mid-ocean ridge geothermal system accompanying basalt alteration.The MgO/FeO ratios of chlorite and actinolite and the Fe₂O₃ concentration of epidote from the basalt are greater than those of mid-ocean ridge basalt probably owing to the differences in the Fe₂O₃/FeO and MgO/FeO ratios of the parent rocks. The lower CaO concentration and the higher Na₂O concentration of the bulk rock compared with altered mid-ocean ridge basalt can be interpreted in terms of the difference in original bulk rock compositions.The Furutobe basalt, as well as other submarine back arc basalts, contains more vesicles filled with hydrothermal minerals (epidote, calcite, quartz, chlorite, pyrite) than do the mid-ocean ridge basalts. The abundance of vesicles plays an important role in controlling the secondary mineralogy and geochemistry of hydrothermally altered submarine back arc basin basalts.     

Coronal structure observed at the total solar eclipse of 11 June, 1983 in Indonesia

From the photographs taken at the total solar eclipse of 11 June 1983, we derived the electron density for the north polar rays and for the thread-like fine structures above the active region, which are 10⁸ at 1.4 solar radii and 3×10⁹ at 1.15 solar radii, respectively. The brightness distributions of the corona at the polar region and above the active region, and the flattening index were also derived.Paper presented at the IAU Third Asian-Pacific Regional Meeting, held in Kyoto, Japan, between 30 September–6 October, 1984.     

Distribution of trace elements during breakdown of mantle garnet: an example from Zabargad

Ion probe investigations on mineral phases forming the Al-Di pyroxenites from the Zabargad peridotite body indicate that porphyroclastic pyroxenes in composite mafic layers record an unusual HREE, Zr, Sc enrichment not registered by pyroxenes in spinel websterites. Orthopyroxene in the opx+sp clusters forming the inner, cpx-free zone of layered pyroxenites shows strongly fractionated REE patterns (HREE_N/LREE_N>1000; Yb>100xch) and very high Zr, Sc and Y abundances (up to 30,672 and 60ppm, respectively). In the outer, cpx-rich zone porphyroclastic clinopyroxene is strongly HREE enriched (HREE_N/LREE_N29; Yb 269xch) and displays very high Sc and Zr abundances (up to 819 and 164 ppm, respectively). It is suggested that the unusual trace element abundances are inherited from a precursor garnet. Composite pyroxenite layers are interpreted as former garnet clinopyroxenites characterized by gnt/cpx modal zoning. The sp+opx(cpx-free) assemblage in the inner part is a product of the break-down reaction of garnet upon decompression, with Ca of the original garnet completely entering the enstatite solid solution. The temperature at which the breakdown reaction occurred is estimated to be higher than 1000°C (P in the range 20–30 kbar). In the outer part, decompression caused the garnet to form a sp+opx assemblage; however, the grossularite component participated in the formation of new clinopyroxene which reacted with the clinopyroxene present in the original mode before the decompression reaction, thus forming a cpx₂+sp+opx assemblage. As a result of garnet breakdown, pyroxenes have peculiar HFSE anomalies. Progressive upwelling during the Red Sea rifting produced incomplete reaction under pl-facies conditions. The geochemical signatures of precursor garnet in pyroxenes were partially crased during the recrystallization from granular spincl-bearing to granoblastic plagioclase-bearing assemblages, being preserved only in a few porphyroclast relies. The finding of pyroxenes with trace element characteristics of precursor garnet has important geodynamic and geochemical implications. Al-Di pyroxenite layers had a long history within the mantle, before the continental lithosphere rifting and thinning took place in the region. It is suggested that Al-Di pyroxenites were formed by deep-seated tholeiitic magmatism unrelated to the Red Sea evolution, thus representing the earliest event in the Zabargad upper mantle. Garnet breakdown significantly preceded the metasomatism induced by hydrous fluids (crystallization of Ti-rich pargasite) and the later intrusion of hydrous (Cr-Di) pyroxenite dykes. During the stages of mantle evolution, the HFSE anomalies in pyroxenes varied significantly. We note that the study of HFSE anomalies in mineral phases reveals complex geochemical histories which are not recorded by the whole-rock system.     

Infiltration of refractory melts into the lowermost oceanic crust: evidence from dunite- and gabbro-hosted clinopyroxenes in the Bay of Islands Ophiolite

Up to 3 km of dunitic rocks occur below crustal gabbro in the Blow Me Down massif (Bay of Islands Ophiolite, Newfoundland). Analyses of dunite- and gabbro-hosted clinopyroxene grains (cpx) for rare earth elements (REE), Zr, and Ti reveal three types of chondrite-normalized patterns: N-group patterns are similar to cpx grains as they would form by fractionation from a range of mid ocean ridge basalts (MORB). They are typical for a few higher level dunitic samples as well as mafic cumulates. F-group patterns show light REE depletion, very strong middle REE fractionation and a positive Zr anomaly and occur in dunites only. R-group patterns are severely depleted in both light and heavy REEs relative to MORB-like cpx and two samples of the group display a positive Ti anomaly. They are also restricted to dunitic rocks. The patterns are explained in a two stage model in which an established dunite sequence, dominated by MORB-type cumulate signatures (N-group), was infiltrated by extremely refractory melts. During infiltration of the refractory melt chromatographic fractionation occurred, transforming N-group dunites into F-group and R-group dunites. The F-group patterns are composite patterns: heavy REE, Ti ± Zr reflect the original MORB-like cumulate dunite host, light REEs indicate equilibrium with the infiltrating, refractory melts. Steep slopes in the middle REEs reflect the position of the chromatographic front. For more intense percolation of refractory melts, R-group patterns with a positive Ti anomaly will form by the same process. The rest of the R-group patterns displaying no positive Ti anomaly may represent either the most intensely reacted host rocks or these dunites derive directly as cumulates from refractory melts. Only small volumes of refractory melt (a 5 m column) are required to imprint the observed trace element pattern on the thick original dunite sequence. One of several possible origins for the refractory melts is transformation of original MORB-type melts by way of chromatographic fractionation within the highly depleted, residual uppermost mantle. In the framework of an oceanic spreading centre, the migrating, refractory liquids are considered a late event following the main constructive stage dominated by aggregated melts. The study demonstrates that highly refractory melts can exist under oceanic spreading centres dominated by a MORB-like cumulate and volcanic sequence. Received: 2 September 1996 / Accepted: 20 November 1997     

Volatiles in the cometary nuclei

The argument for the similarity of the composition of cometary volatiles to that of interstellar molecules has been strengthened by the analysis of CO⁺ and CO ₂ ⁺ emission of the comet West. The strong 6300 Å emission of oxygen atoms can be interpreted in terms of photodissociation of OH by the solar Lyman-alpha radiation, and not as being due to photo-dissociation of CO₂ of speculatively large amount.