ALBERT

Description: This study investigates pressure effects on the magnetic properties of non-interacting single-domain (SD) magnetite. Using a high-pressure cell specially designed for a Magnetic Property Measurement System, magnetic hysteresis measurements were conducted under high pressures of up to 1 GPa on natural plagioclase crystals containing much acicular SD magnetite. Coercivity and saturation magnetization were nearly constant with pressure, while saturation remanent magnetization and coercivity of remanence decreased with pressure at moderate rates of –8 per cent GPa –1 and –18 per cent GPa –1 , respectively. These results suggest that temperature effects govern the magnetic behaviour of acicular SD magnetite grains in the middle and lower crusts.

Description: To investigate the nature and origin of across-arc geochemical variations over time in mantle wedge derived magmas, we have carried out a geochemical study of basalts in the NE Japan arc spanning an age range from 35 Ma to the present. Back-arc basalts erupted at 24–18 Ma, 10–8 Ma, 6–3 Ma and 2·5–0 Ma have higher concentrations of both high field strength elements (HFSE) and rare earth elements (REE) [particularly light REE (LREE) and middle REE (MREE)], and higher incompatible trace element ratios compared with frontal-arc basalts at any given time. Geochemical modeling of Nb/Yb versus Nb shows that the frontal-arc and back-arc compositional differences are independent of subduction modification and can, in many cases, be explained by different degrees of melting (higher degrees of melting for frontal-arc magmas and lower degrees of melting for back-arc magmas) of a nearly homogeneous depleted mid-ocean ridge basalt (MORB) mantle (DMM)-like source, although there are several exceptions. These include some Pliocene frontal-arc basalts that may originate from a source that is slightly more depleted than DMM, several 35–32 Ma and 24–18 Ma back-arc basalts derived from a lithospheric mantle source that is enriched in HFSE compared with DMM, and a rare 16–12 Ma basalt that was erupted in the back-arc but was produced by a similar degree of melting to frontal-arc basalts erupted at the same time. Variations in ratios of fluid-mobile and -immobile elements and those of melt-mobile and -immobile elements for the 35–0 Ma NE Japan basalts indicate that the principal subduction component added to the source mantle prior to generation of these basalt magmas is a sediment-derived melt. Comparison of Sr and Nd isotopic compositions for Pacific Ocean MORB, the NE Japan basalts and subducting sediments suggests that the isotopic compositions of most post-16 Ma more depleted back-arc basalts can be explained by the addition of 〈2% bulk sediment; the most enriched isotope compositions of the subcontinental lithosphere-derived magmas can be accounted for by addition of a maximum 5–7% Japan Trench Sediment (JTS), if the original Sr and Nd compositions of the lithosphere approximated that of DMM. The Sr and Nd isotope composition of the frontal-arc basalts can be accounted for by the addition of 1–5% JTS. A depleted asthenospheric mantle (DMM-like) upwelling model with interaction between asthenospheric mantle-derived magmas and overlying lithospheric mantle can account for the geochemical characteristics of the 35–0 Ma NE Japan basalts. The frontal-arc magmas were generally generated by higher degrees of melting of the shallower part of the asthenospheric mantle, whereas the back-arc magmas resulted from lower degrees of melting of the deeper part of asthenospheric mantle. These latter magmas underwent interaction with the lithospheric mantle, resulting in more enriched Sr and Nd isotopic signatures for the pre-18 Ma back-arc basalts and post-22 Ma frontal-arc basalts, but less interaction, resulting in more depleted Sr and Nd isotopic signatures, for most of the back-arc basalts younger than 16 Ma.

Description: Glycogen phosphorylase (GP) exists in two interconvertible forms, GPa (phosphorylated form, high activity) and GPb (nonphosphorylated form, low activity). Phosphorylase kinase (PhK) catalyses the phosphorylation of GPb and plays a key role in the cascade system for regulating glycogen metabolism. In this study, we developed a highly sensitive and nonradioactive assay for PhK activity by measuring the enhanced GP activity towards a pyridylaminated maltohexaose. The enhanced GP activity ( A ) was calculated by the following formula: A = A + – A 0 , where A + and A 0 represent the GP activities of the PhK-treated and PhK-nontreated samples, respectively. Using a high-performance liquid chromatograph equipped with a fluorescence spectrophotometer, the product of GP activity could be isolated and quantified at 10 fmol. This method does not require the use of any radioactive compounds and only 1 µg of GPb per sample was needed to obtain A + and A 0 values. The remarkable reduction in GPb concentration enabled us to discuss an interesting new role for glycogen in PhK activity.

Description: In this study, we investigated the distribution of small photosynthetic eukaryotes in the near-surface layer of the western North Pacific at four stations, including two oceanic stations where the subarctic Oyashio and subtropical Kuroshio currents influence a transition region and the bay mouth and head of the Sendai Bay, from April 2012 to May 2013. Flow cytometry was applied to sort small photosynthetic eukaryotes (〈5 μm), and high-throughput sequencing of 18S rDNA was performed. Our taxonomic analysis showed that 19/195 operational taxonomic units (OTUs) were frequently distributed among all sites. Composition analysis showed that the OTUs had characteristic patterns and were divided into four main groups. Two groups reflected the low-saline water and winter season, with the characteristic OTUs belonging to diatoms; Chaetoceros and Leptocylindrus were characteristic of low saline water, and two diatom genera ( Minidiscus and Minutocellus ) and Cryptomonadales-related OTUs were prevalent in the winter. Our results indicate that the community composition of small photosynthetic eukaryotes seasonally changes in a dynamic manner according to variations in water properties.