⁴⁰Ar-³⁹Ar geochronological studies on submarine rocks from the western Pacific area     

Kazuo Saito  Minoru Ozima 《Earth and Planetary Science Letters》1977,33(3):353-369

  相似文献   

Sea water weathering effect on K-Ar age of submarine basalts     

Minoru Ozima  Kazuo Saito  Masahiko Honda  Sigeo Aramaki 《Geochimica et cosmochimica acta》1977,41(4):453-461

K-Ar dating and ⁴⁰Ar-³⁹Ar step heating experiments have been done for successive zones from the surface to the interior in two, altered dredged submarine basalts (16-2-6 and Aries V-23). The K contents show a systematic decrease (surface to the interior), whereas the K-Ar ages show a similar decrease in one sample (16-2-6) and almost no change in the other (Aries V-23).A simple diffusion model suggests that the K content decreases systematically from the surface to the interior, whereas the K-Ar age decreases or remains almost constant, depending on whether the times of solidification and of commencement of K-diffusion are close to each other or differ significantly. Comparison of the observed K content and K-Ar age variations within the rocks with the theoretical model then suggests that the solidification age of the sample Aries V-23 is much older than the commencement of the potassium-diffusion, the latter age perhaps being represented by the Eocene planktonic foraminifera on this sample. The ⁴⁰Ar-³⁹Ar isochron age obtained for the freshest specimen of Aries V-23 is 86.6 ± 3.7 m.y., supporting the above conclusion.The mathematical simulation indicates that an apparent concordance of the K-Ar age observed in some submarine basalts may be an artifact, only reflecting the significant gap between the solidification age and the time of the commencement of the K-diffusion in the rocks. Microprobe examination reveals that the potassium enrichment in the outer margin, is mainly due to K feldspar, which is an alteration product of plagioclase.  相似文献   

Measurements of the effective attachment coefficient between RaA ions and condensation nuclei     

Yukimasa Ikebe  Michikuni Shimo  Minoru Kawano 《Pure and Applied Geophysics》1970,83(1):131-141

Summary To clarify the interaction between RaA ions and condensation nuclei, simultaneous measurements of the concentration of RaA ions (n _A), radon-222, and condensation nuclei (Z) were carried out at several stations. In some occasions, the diffusion coefficients of nuclei (D) were also measured. It was found that the correlation among them may be well expressed by the simple formula;q _A = _A n_A Z. The correlation between _A andD (or radius of nuclei) was also obtained.The effective attachment coefficient of RaA ions was compared with that of small ordinary ions, and it was presumed that about one fourth of RaA atoms formed on the decay of radon-222 is positively charged, and the rest is neutral.  相似文献   

Ar isotopes and Earth-atmosphere evolution models     

Minoru Ozima 《Geochimica et cosmochimica acta》1975,39(8):1127-1134

Earth-atmosphere evolution models are mathematically simulated and the resulting present isotopic ratio (⁴⁰Ar/³⁶Ar) in the mantle is given for each.Differential outgassing experiments on several recent submarine glasses were made to estimate an isotopic ratio (⁴⁰Ar/³⁶Ar) in the present mantle. Estimations of (⁴⁰Ar/³⁶Ar) in the mantle by various methods are also critically reviewed. From the experimental results and these considerations a minimum value of 2000 for (⁴⁰Ar/³⁶Ar) ratio in the present mantle is inferred. By assuming that $\text{(}{}^{40}\text{Ar/}{}^{36}\text{Ar)}{}_{\mathrm{M}}$ is larger than 2000 and that the potassium content in the present mantle is larger than 50 ppm, we can limit considerably a choice among various Earth-atmosphere evolution models, i.e. (1) a continuous degassing process can not explain rare gas evolution in the atmosphere, (2) early sudden degassing is more likely and (3) such sudden degassing must have occurred earlier than 4.35 b.y.  相似文献   

Smectite-Zeolite Envelope Surrounding the Tsukiyoshi Uranium Deposit, Central Japan: A Natural Analogue Study     

Minoru Utada 《Resource Geology》2003,53(4):293-304

Abstract. The Tsukiyoshi uranium deposit in Gifu Prefecture is the largest one in Japan. It is embedded in lower part of the Mizunami Group of Miocene age. Relating to the existence of this uranium deposit, the constituent minerals in sediments were studied by XRD and SEM, using many drilling cores. The most abundant authigenic mineral is smectite. The amount of smectite increases generally from upper to lower horizons, and a highly smectitized zone is situated around the uranium deposit. Smectitization predominated in mafic glassy grains of sediments, which was probably formed in early burial diagenesis. Zeolites including clinoptilolite-heulandite, mordenite, analcime, chabazite and philipsite are secondly abundant authigenic minerals. They seem to have been formed at early to late diagenetic stages. Opaline silica is rather rare. Carbonate minerals, including cal-cite, dolomite, siderite and rhodochrosite are common. They may be formed by diagenesis as well. Gypsum and pyrite occur in upper horizons and lower horizons, respectively. In particular, a highly smectitized zone including pyrite probably played an important role for retarding the migration of uranium and as a result keeping the uranium deposit for past one million years. This smectite-zeolite envelope surrounding the Tsukiyoshi uranium deposit is regarded as a natural analogue of the buffer materials surrounding the high-level radioactive waste repository.  相似文献   

Deep-sea coral geochemistry: Implication for the vital effect   总被引：2，自引：0，他引：2  

Kotaro Shirai  Minoru Kusakabe  Teruaki Ishii  Hajime Hiyagon 《Chemical Geology》2005,224(4):212-222

Deep-sea corals hold a great potential as a key to important aspects of paleoceanography for at least two reasons, 1) they offer temporal high resolution records of deep-sea environment, because they have growth banding structures, 2) and they are well suited for studying vital effects, because the deep-sea environment does not change over short time scales. However, the relationship between the chemical composition of deep-sea coral skeletons and environmental factors is not well understood. In this study, the chemical composition of deep-sea corals was measured in bulk individuals and along skeletal micro-structures. Among the bulk individuals, δ¹⁸O value and Sr / Ca ratio show a negative but weak correlation with ambient temperature. On the other hand, the Mg / Ca ratio has a positive, weak correlation with the temperature. Large variations were found among samples collected from similar temperature. The variation is up to 3.8‰ for δ¹⁸O, 0.9 mmol/mol for Sr / Ca ratios, and 0.78 mmol/mol for Mg / Ca ratios among samples with ambient average temperature within 1 °C. This variation may be due to a large vital effect. The centers of calcification (COCs), which were formed at high calcification rate, have lower Sr / Ca, U / Ca and higher Mg / Ca ratios than surrounding fasciculi. This chemical distribution supports the model that elemental incorporation depends on calcification rate. This suggests that calcification rate is a very important factor for the chemical composition in deep-sea corals and is one of the most significant mechanisms of the vital effect. Because of this large vital effect, further investigations are essential to use the deep-sea coral as a temperature proxy.  相似文献   

What can be learned from rotational motions excited by earthquakes?   总被引：1，自引：0，他引：1  

Minoru Takeo  Hidemi M. Ito 《Geophysical Journal International》1997,129(2):319-329

One answer to the question posed in the title is that we will have more accurate data for arrival times of SH waves, because the rotational component around the vertical axis is sensitive to SH waves although not to P-SV waves. Importantly, there is another answer related to seismic sources, which will be discussed in this paper.
Generally, not only dislocations commonly used in earthquake models but also other kind of defects could contribute to producing seismic waves. In particular, rotational strains at earthquake sources directly generate rotational components in seismic waves. Employing the geometrical theory of defects, we obtain a general expression for the rotational motion of seismic waves as a function of the parameters of source defects.
Using this expression, together with one for translational motion, we can estimate the rotational strain tensor and the spatial variation of slip velocity in the source area of earthquakes. These quantities will be large at the edges of a fault plane due to spatially rapid changes of slip on the fault and/or a formation of tensile fractures.  相似文献   

S, O and Sr isotope systematics of active vent materials from the Mariana backarc basin spreading axis at 18°N     

Minoru Kusakabe  Shingo Mayeda  Eizo Nakamura 《Earth and Planetary Science Letters》1990,100(1-3)

Stable isotope ratios of S, O and Sr have been measured for active vent materials which were first found and sampled in April 1987 from the Mariana backarc spreading axis at 18°N. Chimneys consisted mostly of barite with a lesser proportion of sulfide minerals such as sphalerite, galena, chalcopyrite and pyrite. Theδ³⁴S values of sphalerite and galena taken from several chimneys and various parts of a chimney showed a narrow range from 2.1 to 3.1‰, suggesting uniform conditions of fluid chemistry during chimney growth. The sulfur isotopic results imply a contribution of hydrogen sulfide reduced from seawater sulfate in the deep hydrothermal reaction zone, considering that fresh glasses of the Mariana Trough basalts haveδ³⁴S= −0.6 ± 0.3‰. Sulfur isotopic compositions of hydrogen sulfide in the high temperature vent fluids (δ³⁴S= 3.6–4.8‰) which are higher than those of the sulfide minerals suggest the secondary addition of hydrogen sulfide partially reduced from entrained seawater SO₄²⁻ at a basal part of the chimneys. This interpretation is consistent with theδ³⁴S values of barite (21–22‰) that are higher than those of seawater sulfate. The residence time of the entrained SO₄²⁻ was an order of an hour on a basis of oxygen isotopic disequilibrium of barite. Strontium isotopic variations of barite and vent waters indicated that Sr in barite was mostly derived from the Mariana Trough basalts with a slight contribution from Sr in circulating sea-water, and that 10–20% mixing of seawater with ascending hydrothermal fluids induced precipitation of barite at the sea-floor.  相似文献   

Strontium, oxygen, and hydrogen isotope geochemistry of hydrothermally altered and weathered rocks in DSDP Hole 504B, Costa Rica Rift     

Hodaka Kawahata  Minoru Kusakabe  Yoshiko Kikuchi 《Earth and Planetary Science Letters》1987,85(4)

DSDP Hole 504B was drilled into 6 Ma crust, about 200 km south of the Costa Rica Rift, Galapagos Spreading Center, penetrating 1.35 km into a section that can be divided into four zones—Zone I: oxic submarine weathering; Zone II: anoxic alteration; Zones III and IV: hydrothermal alteration to greenschist facies. In Zone III there is intense veining of pillow basalts. Zone IV consists of altered sheeted dikes. Isotopic geochemical signatures in relation to the alteration zones are recorded in Hole 504B, as follows:Alteration temperatures are as low as 10°C in Zones I and II based on oxygen isotope fractionation. Strontium isotopic data indicate that a circulation of seawater is much more restricted in Zone II than in Zone I. Fluid inclusion measurements of vein quartz indicate the alteration temperature was mainly 300 ± 20°C in Zones III and IV, which is consistent with secondary mineral assemblages.The strontium, oxygen, and hydrogen isotopic compositions of hydrothermal fluids which were responsible for the greenschist facies alteration in Zones III and IV are estimated to be 0.7037, 2‰, and 3‰, respectively. Strontium and oxygen isotope data indicate that completely altered portions of greenstones and vein minerals were in equilibrium with modified seawater under low water/rock ratios (in weight) of about 1.6. This value is close to that of the end-member hydrothermal fluids issuing at 21°N EPR.Basement rocks are not completely hydrothermally altered. About 32% of the greenstones in Zones III and IV have escaped alteration. Thus 1 g of fresh basalt including the 32% unaltered portion are required in order to make 1 g of end-member solution from fresh seawater in water-rock reactions.  相似文献   

On the sensitivity characteristics of Lacoste & Romberg gravimeter (model G)     

Ichiro Nakagawa  Sinzi Nakai  Ryūichi Shichi  Hirokazu Tajima  Sadakatu Izutuya  Yoshiteru Kono  Toshihiro Higashi  Hiromi Fujimoto  Makoto Murakami  Kazuo Tajima  Minoru Funaki 《Journal of Geodesy》1985,59(1):55-67

  相似文献