Phytoplankton communities in the Bering Sea and adjacent seas

Vertical distribution of phytoplankton in early warming season in the eastern Bering Sea and adjacent sea areas was investigated. In the surface layer which was under the influence of newly melted sea ice in the shelf water region of the Bering Sea in May, remarkably dense populations ofThalassiosira hyalina andT. nordenskiöldii and relatively large populations ofFragilaria andNavicula occupied large part of phytoplankton community. In June, although theThalassiosira populations sunk into the bottom layer and withered, a certain part of theFragilaria-Navicula populations was still suspended in subsurface layer. Thus,Fragilaria-Navicula were the leading components of the June community in the shelf region.In the Bering Basin region, no dense phytoplankton populations were developed until a shallow thermocline was established. In June when the shallow thermocline developed near shelf edge,Thalassiosira decipiens burst out. As the shallow thermocline extended from near shelf to central part of the Basin region with surface warming, the areas of blooming also shifted from near shelf to the central part.Contribution No. 73 from the Research Institute of North Pacific Fisheries, Hokkaido University.     

Mineralogical and Geochemical Constraints on Arsenic Mobility in a Philippine Geothermal Field

Arsenic is usually associated with sulphide minerals formed in the geothermal environment. However, sulphide minerals are prone to dissolution after contact with meteoric water under surface oxidizing conditions. Secondary precipitates that form from the dissolution of the primary sulfides exert a greater influence on arsenic mobility in the geothermal environment. Fe-hydroxides have very good affinity with dissolved arsenate and are stable under most surface oxidizing conditions. Both amorphous silica directly precipitated from geothermal fluids and possibly a kaolinite alteration can host a small significant amount of arsenic. These silicates are also more stable under a wide range of pH and redox conditions.     

在可控制的相对湿度下矿物表面上多环芳烃的降解

多环芳香烃由于诱发突变和致癌的性质威胁着人类的健康,近年来,其降解问题得到了广泛的关注。笔者研究了在没有光照的条件下,改变相对湿度(5%至30%之间),苯并芘(一种典型的多环芳烃物质)在石英,矾土,蒙脱石,高岭石,腐殖酸和吸附了腐殖酸的石英上的稳定性,继而可以检测出矿物表面催化多环芳烃降解的效果。苯并芘的稳定性主要是由吸附剂的物化性质决定的。石英表现出很好的催化效果,即便其表面被腐殖酸所包覆。在整个实验过程中(3天)吸附在蒙脱石和腐殖酸表面的苯并芘依然很稳定。实验装置中的湿度影响在某些特定的矿物中的苯并芘的稳定性。特…     

Experimental Petrology of the 1991-1995 Unzen Dacite, Japan. Part II: Cl/OH Partitioning between Hornblende and Melt and its Implications for the Origin of Oscillatory Zoning of Hornblende Phenocrysts

High-temperature–pressure experiments were carried outto determine the chlorine–hydroxyl exchange partitioncoefficient between hornblende and melt in the 1992 Unzen dacite.Cl in hornblende and melt was analyzed by electron microprobe,whereas OH in hornblende and melt was calculated assuming anionstoichiometry of hornblende and utilizing the dissociation reactionconstant for H₂O + O = 2(OH) in water-saturated melt, respectively.The partition coefficient strongly depends on the Mg/(Mg + Fe)ratio of hornblende, and is expressed as ln K₁ = (Cl/OH)_hb/(Cl/OH)_melt= 2·37 – 4·6[Mg/(Mg + Fe)]_hb at 2–3kbar and 800–850°C. The twofold variation in Cl contentin the oscillatory zoned cores of hornblende phenocrysts inthe 1991–1995 dacite cannot be explained by the dependenceof the Cl/OH partition coefficient on the Mg/(Mg + Fe)_hb ratio,and requires c. 80% variation of the Cl/OH ratio of the coexistingmelt. Available experimental data at 200 MPa on Cl/OH fractionationbetween fluid and melt suggest that c. 1·2–1·8wt % degassing of water from the magma can explain the required80% variation in the Cl/OH ratio of the melt. The negative correlationbetween Al content and Mg/(Mg + Fe) ratio in the oscillatoryzoned cores of the hornblende phenocrysts is consistent withrepeated influx and convective degassing of the fluid phasein the magma chamber. KEY WORDS: chlorine; element partitioning; hornblende; oscillatory zoning; Unzen volcano     

An automated precise Winkler titration for determining dissolved oxygen on board ship

An automated titration for the Winkler method is presented for measuring primary productivity in the ocean. The system is based on a microcomputer-controlled titration with potentiometric endpoint detection. By the use of 0.005-N sodium thiosulfate as a titrant and a program designed to shorten the time for measuring, the method achieves a precision of 0.04% coefficient of variation with a range of 0.01 to 0.10% for six replicates of samples at oxygen concentration of 70 to 250 M. It takes about four to five minutes to measure one sample.     

ELECTRICAL SOUNDING OF A HALF-SPACE WITH A MONOTONIC CONTINUOUS VARIATION OF THE RESISTIVITY WITH DEPTH*

The interpretation of electrical sounding data for a subsurface with monotonic continuous variation of the resistivity with depth is becoming increasingly necessary. The contribution of this article is the derivation of the solution for the Wenner and the Schlumberger apparent resistivity functions for a resistivity varying as a real power of a linear positive function of the depth. The interpretation of sounding data in these cases can be used to estimate the variation of the porosity or the salt content of the pore water with depth.     

Mid–Cretaceous Episodic Magmatism and Tin Mineralization in Khingan-Okhotsk Volcano–Plutonic Belt, Far East Russia

Abstract: Age of magmatism and tin mineralization in the Khingan‐Okhotsk volcano–plutonic belt, including the Khingan, Badzhal and Komsomolsk tin fields, were reviewed in terms of tectonic history of the continental margin of East Asia. This belt consists mainly of felsic volcanic rocks and granitoids of the reduced type, being free of remarkable geomagnetic anomaly, in contrast with the northern Sikhote‐Alin volcano–plutonic belt dominated by oxidized‐type rocks and gold mineralization. The northern end of the Khingan‐Okhotsk belt near the Sea of Okhotsk, accompanied by positive geomagnetic anomalies, may have been overprinted by magmatism of the Sikhote‐Alin belt. Tin–associated magmatism in the Khingan‐Okhotsk belt extending over 400 km occurred episodically in a short period (9510 Ma) in the middle Cretaceous time, which is coeval with the accretion of the Kiselevka‐Manoma complex, the youngest accretionary wedge in the eastern margin of the Khingan‐Okhotsk accretionary terranes. The episodic magmatism is in contrast with the Cretaceous‐Paleogene long–lasted magmatism in Sikhote–Alin, indicating the two belts are essentially different arcs, rather than juxtaposed arcs derived from a single arc. The tin‐associated magmatism may have been caused by the subduction of a young and hot back‐arc basin, which is inferred from oceanic plate stratigraphy of the coeval accre‐tionary complex and its heavy mineral assemblage of immature volcanic arc provenance. The subduction of the young basin may have resulted in dominance of the reduced‐type felsic magmas due to incorporation of carbonaceous sediments within the accretionary complex near the trench. Subsequently, the back‐arc basin may have been closed by the oblique collision of the accretionary terranes in Sikhote–Alin, which was subjected to the Late Cretaceous to Paleogene magmatism related to another younger subduction system. These processes could have proceeded under transpressional tectonic regime due to oblique subduction of the paleo‐Pacific plates under Eurasian continent.     

Decomposition of Polycyclic Aromatic Hydrocarbon （PAHs） on Mineral Surface under Controlled Relative Humidity

The fate of Polycyclic Aromatic Hydrocarbons （PAHs） residing in the atmosphere has received enormous attention in recent years due to their mutagenic and carcinogenic risks on human health. In this context, the stability of pyrene （as a representative PAHs） on quartz, alumina, montmorillonite, kaolinite, humic acid and quartz coated with sorbed humic acid was investigated at controlled relative humidity （RH： i.e. 5% and 30%） without light irradiation in order to detect the presence of catalytic effect of mineral surface on PAHs decomposition. The stability of pyrene was found to depend strongly on the physicochemical properties of the substrates. Quartz showed a strong catalytic effect for the decomposition of pyrene even though it was coated with sorbed humic acid. Pyrene sorbed on montmorillonite and humic acid remained stable during the experimental period （i.e. 3 days）. Moisture in the experimental cell also affected the stability of pyrene in particular minerals. Especially, pyrene sorbed on alumina was rapidly decomposed at higher RH. However, there were almost no effect in the case of quartz, kaolinite and humic acid. Depending on the physicochemical properties of aerosols and RH, PAHs associated with minerals in the atmosphere would be decomposed and/or stably reside in the atmosphere.     

White light events as photospheric flares

We consider the possibility that white light flares are due to heating of the photosphere by a flux of energetic ions and electrons impinging on it from above. Particles with energy in the range 10 MeV to 1 BeV release most of their energy to the ambient gas at about optical depth unity in the photosphere. This increase in energy produces a temperature perturbation of several hundred degrees in the layer and results in a re-radiation of the energy with a radiative relaxation time of several seconds. The consequences of this model are applied to a study of the great flare of May 23, 1967 and to the very fast event of August 11, 1954. Large numbers of very energetic electrons or protons must be produced in the first few minutes of the primary flare event if our interpretation (or one based on synchrotron emission) is correct.After this paper had been submitted and accepted for publication we received from Dr. vestka a copy of his paper, The Phase of Particle Acceleration in the Flare Development, which was then already in proof. (It appeared in Solar Phys. 13, 471.) A number of the arguments contained in our paper, which we had previously presented in abstract form (Najita and Orrall, 1969) and in part in a dissertation (Najita, 1969), are independently discussed by Dr. vestka who was unaware of our earlier work. Although the ground covered by his and our paper touches in places we have left our paper as originally submitted and believe that this independent agreement supports the conclusions of both.     

Adsorption of tributyltin by tributyltin resistant marine Pseudoalteromonas sp. cells

The isolate, Pesudoalteromonas sp. TBT1, could grow to overcome the toxicity of tributyltin chloride (TBTCl) up to 30 microM in the absence of Cl(-) in the medium until the cells reached an exponential phase of growth. The viability, however, was reduced after the cells reached a stationary phase. The degradation products, such as dibutyltin (DBT) and monobutyltin (MBT), were not detected in the growth medium, indicating that the isolate has no ability to degrade TBT into less toxic DBT and MBT. Up to about 10(7.5) TBT molecules were adsorbed by a single cell. The observation of morphological changes with an electron microscope showed that the cell surface became wrinkled after exposure to the lethal concentration of 10 mM TBTCl. These results indicate that the resistance of the isolate toward the toxicity of TBTCl is not related to the unique cell surface, which seems to play an important role in preventing the diffusion of TBTCl into the cytoplasm.