A simple indirect method for the determination of organic-carbon in marine particles     

Shinichiro Noriki  Chizuru Saito  Shizuo Tsunogai 《Journal of Oceanography》1990,46(3):135-138

A simple indirect method for the determination of organic carbon in marine particulate matter is proposed. The recommended procedure is as follows: The dried sample is ashed at 450°C for about 24 hr. The ashed sample is put into a Teflon vessel followed by a mixed solution of nitric acid, perchloric acid and hydrofluoric acid. The vessel is sealed and allowed to stand at 150°C for 5 hr. The concentrations of Si and Al in the digested solution are determined. The organic carbon content (Cal-C, %) is calculated by the following equation: Cal-C=0.52 ([CF]–0.10 [Opal]–0.03 [A-Si]), where [CF] is the combustible fraction (%), [Opal] is the biogenic-SiO₂(%), and [A-Si] is the content of aluminosilicate mineral (%).  相似文献   

Regeneration of chemical elements from settling particles collected by sediment trap in Funka Bay,Japan     

Shinichiro Noriki  Norihito Ishimori  Shizuo Tsunogai 《Journal of Oceanography》1985,41(2):113-120

Sediment trap experiments were carried out 39 times during the years from 1977 to 1981 in Funka Bay, Hokkaido, Japan. The observed total particulate flux varies seasonally, that is, the particulate fluxes in winter and spring are larger than those in summer. The fluxes in all seasons increased with depth. Major components of settling particles are aluminosilicate in winter, biogenic silicate in spring and organic matter and terrestrial material in summer, respectively. The fluxes of each chemical component observed with sediment traps are normalized to that of Al by assuming that the actual flux of Al is equal to the accumulation rate onto the sediment surface. Vertical changes of the normalized flux of each chemical component indicate the following: Fe was not regenerated from the settling particles in the water column. Mn was regenerated from the settling particles in the lower layer exclusively between 80 m depth and the sediment surface. Cd was actively regenerated in the upper layer above 80 m depth. Phosphate was regenerated in the upper layer, while biogenic silicate was in the lower layer. The silicate regeneration, therefore, occurs after phosphate regeneration. The material decomposing in the water column below 40 m has an atomic ratio of P ∶ Si ∶ C = 1 ∶ 52 ∶ 128.  相似文献   

Evaluation of predictors of non‐linear seismic demands using ‘fishbone’ models of SMRF buildings     

Nicolas Luco  Yasuhiro Mori  Yosuke Funahashi  C. Allin Cornell  Masayoshi Nakashima 《地震工程与结构动力学》2003,32(14):2267-2288

Predictors (or estimates) of seismic structural demands that are less computationally time‐consuming than non‐linear dynamic analysis can be useful for structural performance assessment and for design. In this paper, we evaluate the bias and precision of predictors that make use of, at most, (i) elastic modal vibration properties of the given structure, (ii) the results of a non‐linear static pushover analysis of the structure, and (iii) elastic and inelastic single‐degree‐of‐freedom time‐history analyses for the specified ground motion record. The main predictor of interest is an extension of first‐mode elastic spectral acceleration that additionally takes into account both the second‐mode contribution to (elastic) structural response and the effects of inelasticity. This predictor is evaluated with respect to non‐linear dynamic analysis results for ‘fishbone’ models of steel moment‐resisting frame (SMRF) buildings. The relatively small number of degrees of freedom for each fishbone model allows us to consider several short‐to‐long period buildings and numerous near‐ and far‐field earthquake ground motions of interest in both Japan and the U.S. Before doing so, though, we verify that estimates of the bias and precision of the predictor obtained using fishbone models are effectively equivalent to those based on typical ‘full‐frame’ models of the same buildings. Copyright © 2003 John Wiley & Sons, Ltd.  相似文献   

Mineralogy and geochemistry of granitoids from Kinnaur region,Himachal Higher Himalaya,India: Implication on the nature of felsic magmatism in the collision tectonics     

Brajesh Singh  Santosh Kumar  Masao Ban  Kazuo Nakashima 《Journal of Earth System Science》2016,125(7):1329-1352

Felsic magmatism in the southern part of Himachal Higher Himalaya is constituted by Neoproterozoic granite gneiss (GGn), Early Palaeozoic granitoids (EPG) and Tertiary tourmaline-bearing leucogranite (TLg). Magnetic susceptibility values (<3 ×10^?3 SI), molar Al₂ O ₃/(CaO + Na₂ O + K ₂O) (≥1.1), mineral assemblage (bt–ms–pl–kf–qtz ± tur ± ap), and the presence of normative corundum relate these granitoids to peraluminous S-type, ilmenite series (reduced type) granites formed in a syncollisional tectonic setting. Plagioclase from GGn (An₁₀–An₃₁) and EPG (An₁₅–An₃₃) represents oligoclase to andesine and TLg (An₂–An₁₅) represents albite to oligoclase, whereas compositional ranges of K-feldspar are more-or-less similar (Or₈₈ to Or₉₅ in GGn, Or₈₆ to Or₉₇ in EPG and Or₈₇ to Or₉₄ in TLg). Biotites in GGn (Mg/Mg + Fe^t= 0.34–0.45), EPG (Mg/Mg + Fe^t= 0.27–0.47), and TLg (Mg/Mg + Fe^t= 0.25–0.30) are ferribiotites enriched in siderophyllite, which stabilised between FMQ and HM buffers and are characterised by dominant 3Fe\(\rightleftharpoons \)2Al, 3Mg\(\rightleftharpoons \)2Al substitutions typical of peraluminous (S-type), reducing felsic melts. Muscovite in GGn (Mg/Mg + Fe^t=0.58–0.66), EPG (Mg/Mg + Fe^t=0.31?0.59), and TLg (Mg/Mg + Fe^t=0.29–0.42) represent celadonite and paragonite solid solutions, and the tourmaline from EPG and TLg belongs to the schorl-elbaite series, which are characteristics of peraluminous, Li-poor, biotite-tourmaline granites. Geochemical features reveal that the GGn and EPG precursor melts were most likely derived from melting of biotite-rich metapelite and metagraywacke sources, whereas TLg melt appears to have formed from biotite-muscovite rich metapelite and metagraywacke sources. Major and trace elements modelling suggest that the GGn, EPG and TLg parental melts have experienced low degrees (～13, ～17 and ～13%, respectively) of kf–pl–bt fractionation, respectively, subsequent to partial melting. The GGn and EPG melts are the results of a pre-Himalayan, syn-collisional Pan-African felsic magmatic event, whereas the TLg is a magmatic product of Himalayan collision tectonics.  相似文献   

Implications of Japan’s long term climate mitigation target and the relevance of uncertain nuclear policy     

Diego Silva Herran  Shinichiro Fujimori  Mikiko Kainuma 《Climate Policy》2019,19(9):1117-1131

Achieving long-term climate mitigation goals in Japan faces several challenges, starting with the uncertain nuclear power policy after the 2011 earthquake, the uncertain availability and progress of energy technologies, as well as energy security concerns in light of a high dependency on fuel imports. The combined weight of these challenges needs to be clarified in terms of the energy system and macroeconomic impacts. We applied a general equilibrium energy economic model to assess these impacts on an 80% emission reduction target by 2050 considering several alternative scenarios for nuclear power deployment, technology availability, end use energy efficiency, and the price of fossil fuels. We found that achieving the mitigation target was feasible for all scenarios, with considerable reductions in total energy consumption (39%–50%), higher shares of low-carbon sources (43%–72% compared to 15%), and larger shares of electricity in the final energy supply (51%–58% compared to 42%). The economic impacts of limiting nuclear power by 2050 (3.5% GDP loss) were small compared to the lack of carbon capture and storage (CCS) (6.4% GDP loss). Mitigation scenarios led to an improvement in energy security indicators (trade dependency and diversity of primary energy sources) even in the absence of nuclear power. Moreover, preliminary analysis indicates that expanding the range of renewable energy resources can lower the macroeconomic impacts of the long term target considerably, and thus further in depth analysis is needed on this aspect.

Key policy insights

• For Japan, an emissions reduction target of 80% by 2050 is feasible without nuclear power or CCS.

• The macroeconomic impact of such a 2050 target was largest without CCS, and smallest without nuclear power.

• Energy security indicators improved in mitigation scenarios compared to the baseline.

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Database of molecular masers and variable stars     

Andrej M.Sobolev  Dmitry A.Ladeyschikov  Jun-ichi Nakashima 《天文和天体物理学研究(英文版)》2019,(3):13-20

We present the database of maser sources in H2 O, OH and Si O lines that can be used to identify and study variable stars at evolved stages. Detecting the maser emission in H2 O, OH and Si O molecules toward infrared-excess objects is one of the methods for identifing long-period variables(LPVs, including miras and semiregulars), because these stars exhibit maser activity in their circumstellar shells. Our sample contains 1803 known LPV objects. Forty-six percent of these stars(832 objects) manifest maser emission in the line of at least one molecule: H2 O, OH or Si O. We use the database of circumstellar masers in order to search for LPVs which are not included in the General Catalogue of Variable Stars(GCVS). Our database contains 4806 objects(3866 objects without associations in GCVS) with maser detection in at least one molecule. Therefore it is possible to use the database in order to locate and study the large sample of LPV stars. The database can be accessed at http://maserdb.net.  相似文献   

Mechanism of enrichment of trace metals on fine sludges collected from filtration plants     

Hisayuki Teraoka  Susumu Nakashima 《Environmental Geology》1990,16(2):143-148

Fine sludges were collected from five filtration plants, and the partitioning of ten metals (Ag, Cd, Mn, Zn, Pb, Cu, Sn, Co, Ni, and Fe) in them was determined by selective leaching techniques. (1) The available amounts, which shows the total of each metal leached between 1 M CH₃COONH₄ and 30 percent H₂O₂, for Ag, Cd and Mn, ranged from 51 to 98 percent for five sludges. (2) The available amounts for Zn, Pb, Cu, and Sn were 47–92 percent for five sludges. (3) The most important fraction for Co, Ni, and Fe, except the Inagawa sludge, which is markedly polluted by organic matter, was the crystalline particle. Therefore, the above metals, except Co, Ni, and Fe, are thought to be enriched on ion-exchangeable sites, organic matter, hydrous Fe/Mn oxides, and sulfides in fine sludges.  相似文献   

Trophic relationships among capelin (Mallotus villosus) and seabirds in a changing ecosystem     

Carscadden  J. E.; Montevecchi  W. A.; Davoren  G. K.; Nakashima  B. S. 《ICES Journal of Marine Science》2002,59(5):1027-1033

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Heavily fractionated noble gases in an acid residue from the Klein Glacier 98300 EH3 chondrite     

Daisuke Nakashima  Ulrich Ott  Tomoki Nakamura 《Geochimica et cosmochimica acta》2010,74(17):5134-5149

Noble gases were measured both in bulk samples (stepped pyrolysis and total extraction) and in a HF/HCl residue (stepped pyrolysis and combustion) from the Klein Glacier (KLE) 98300 EH3 chondrite. Like the bulk meteorite and as seen in previous studies of bulk type 3 E chondrites (“sub-Q”), the acid residue contains elementally fractionated primordial noble gases. As we show here, isotopically these are like those in phase-Q of primitive meteorites, but elementally they are heavily fractionated relative to these. The observed noble gases are different from “normal” Q noble gases also with respect to release patterns, which are similar to those of Ar-rich noble gases in anhydrous carbonaceous chondrites and unequilibrated ordinary chondrites (with also similar isotopic compositions). While we cannot completely rule out a role for parent body processes such as thermal and shock metamorphism (including a later thermal event) in creating the fractionated elemental compositions, parent body processes in general seem not be able to account for the distinct release patterns from those of normal Q noble gases. The fractionated gases may have originated from ion implantation from a nebular plasma as has been suggested for other types of primordial noble gases, including Q, Ar-rich, and ureilite noble gases. With solar starting composition, the corresponding effective electron temperature is about 5000 K. This is lower than inferred for other primordial noble gases (10,000-6000 K). Thus, if ion implantation from a solar composition reservoir was a common process for the acquisition of primordial gas, electron temperatures in the early solar system must have varied spatially or temporally between 10,000 and 5000 K.Neon and xenon isotopic ratios of the residue suggest the presence of presolar silicon carbide and diamond in abundances lower than in the Qingzhen EH3 and Indarch EH4 chondrites. Parent body processes including thermal and shock metamorphism and a late thermal event also cannot be responsible for the low abundances of presolar grains. KLE 98300 may have started out with smaller amounts of presolar grains than Qingzhen and Indarch.  相似文献   

Geochemical Characteristics,Origin, and Evolution of Ore‐Forming Fluids of the Khut Copper Skarn Deposit,West of Yazd in Central Iran     

Azam Zahedi  Mohammad Boomeri  Kazuo Nakashima  Mohammad Ali Mackizadeh  Masao Ban  David R. Lentz 《Resource Geology》2014,64(3):209-232

The Khut copper skarn deposit is located at about 50 km northwest of Taft City in Yazd province in the middle part of the Urumieh‐Dokhtar magmatic arc. Intrusion of granitoid of Oligocene–Miocene age into carbonate rocks of the Triassic Nayband Formation led to the formation of marble and a calcic skarn. The marble contains high grade Cu mineralization that occurs mainly as open space filling and replacement. Cu‐rich sulfide samples from the mineralized marble are also anomalous in Au, Zn, and Pb. In contrast, the calcic skarn is only weakly anomalous in Cu and W. The calcic skarn is divided into garnet skarn and garnet–pyroxene skarn zones. Paragenetic relationships and microthermometric data from fluid inclusions in garnet and calcite indicate that the compositional evolution of skarn minerals occurred in three main stages as follows. (i) The early prograde stage, which is characterized by Mg‐rich hedenbergite (Hd_53.7Di_42.3–Hd_86.1Di_9.5) with Al‐bearing andradite (69.8–99.5 mol% andradite). The temperature in the early prograde skarn varies from 400 to 500°C at 500 bar. (ii) The late prograde stage is manifested by almost pure andradite (96.2–98.4 mol% andradite). Based on the fluid inclusion data from garnet, fluid temperature and salinity in this stage is estimated to vary from 267 to 361°C and from 10.1 to 21.1 wt% NaCl equivalent, respectively. Pyrrhotite precipitation started during this stage. (iii) The retrograde stage occurs in an exoskarn, which consists of an assemblage of ferro‐actinolite, quartz, calcite, epidote, chlorite, sphalerite, pyrite, and chalcopyrite that partially replaces earlier mineral assemblages under hydrostatic conditions during fracturing of the early skarn. Fluids in calcite yielded lower temperatures (T < 260°C) and fluid salinity declined to ～8 wt% NaCl equivalent. The last stage mineralization in the deposit is supergene weathering/alteration represented by the formation of iron hydroxide, Cu‐carbonate, clay minerals, and calcite. Sulfur isotope data of chalcopyrite (δ³⁴S of +1.4 to +5.2‰) show an igneous sulfur source. Mineralogy and mineral compositions of the prograde assemblage of the Khut skarn are consistent with deposition under intermediately oxidized and slightly lower fS₂ conditions at shallow crustal levels compared with those of other typical Fe‐bearing Cu–Au skarn systems.  相似文献