The mechanism of the development of wind-wave spectra

The mechanism of the development of wind-waves will be proposed on the basis of the observed wave spectra in the wind tunnels and at Lake Biwa (Imasato, 1976). It consists of two aspects: One is that the air flow over the wind-waves transfers momentum concentratively to the steepest component waves and the other is that the upper limit of the growth of a wave spectral density is given by the ultimate value in the slope spectral density. The first aspect means that the wave field has the momentum transfer filter on receiving the momentum from the air flow. Wind-waves in the stage of sea-waves receive the necessary amount of momentum by the form drag,e.g. according to the Miles' (1960) inviscid mechanism, through a very narrow frequency region around a dominant spectral peak. On the other hand, wind-waves in the stage of initial-wavelets receive it according to the Miles' (1962a) viscous model through a fairly broad frequency region around the peak. The upper limit ofS _max developing according to viscous mechanism is given byS _max =6.40×10^–4 k _max ^–2cm²s andS _max =2.03C(f _max )^–2cm²s(S _max is the power density of the wave spectral peak with the frequencyf _max ,k _max is the wave number corresponding to the frequencyf _max andC is the phase velocity).From the second aspect, the upper limit of the growth of wave spectral density is given by 33.3f ^–4cm²s in the frequency region of late stage of sea-waves. Therefore, the spectral peak, which has the largest value in the slope spectral density in the component waves of the wave spectrum, rises high over the line 4.15f ^–5cm²s. The energy is transported from the spectral peak to the high frequency part and to the forward face of a wave spectrum by nonlinear wave-wave interaction. This nonlinearity is confirmed by the bispectra calculated from the observed wind-wave data. In the stage of sea-waves, nonlinear rearrangement of the wave energy comes from a narrow momentum transfer filter, and, in the stage of initial-wavelets, it comes mainly from small corrugations and small steepness of the wave field.     

Bispectra of wind-waves and wave-wave interaction

Bispectra of wind-waves in wind tunnels were calculated in order to understand the characteristics of the nonlinear wave-wave interaction in actual wind-wave field. It is shown that the nonlinearity in wind-waves increases in magnitude with the development of wind-waves and that the characteristics of nonlinearity in wind-waves in the early stage of development differ from those in the late stage. It is shown that the bispectra are classified into five types (IV), and that the bispectral type changes from the type I to the type V as the wind-waves develop from the stage of the initial-wavelets to that of the sea-waves. The relations between frequencies of the component waves interacting each other are discussed in each bispectral type.     

Nonlinearity of the horizontal velocity field under wind-waves

Using the data from a wind-tunnel experiment, bispectra of orbital-motions of wind-waves and of turbulence are calculated, and nonlinear interaction of wind-waves with turbulence in water are discussed. The wind-waves or the orbital motions of them, at first, produce the turbulence coherent with themselves, and then this coherent turbulence changes to the turbulence noncoherent with wind-waves. Nonlinearity of the velocity fluctuations in the surface layer in water under wind-waves is almost due to the nonlinear energy transfer from the orbital motions of wind-waves to the coherent turbulence. The vertical variations of the power spectra and of the normalized bispectra suggest that the wind driven currents near the surface play an important role in the process from orbital motion of wind-waves to noncoherent turbulence.     

Parameterization of the dispersion relation of internal waves using the data of hydrological soundings in the Tropical Atlantic

Dependences have been determined which connect the parameters of the dispersion relation of the lowest mode of internal waves with the integral characteristics of the seasonal thermocline when 10 min30 min, 20 mh150 m, and 0·4 m²/s² Q5·2 m²/s².Translated by Mikhail M. Trufanov.     

Calcium-alkalinity relationship in the North Pacific

The dissolution of calcium carbonate in deep ocean water causes variation in calcium concentration (Ca) and alkalinity (TA) in the ratio of one to two. The decomposition of organic matter generates nitric acid, phosphoric acid and sulfuric acid. A proton flux which is derived from this process also changes alkalinity. Using the variation in nitrate concentration (NO₃) as an index of the proton flux, the relationship betweenCa,TA andNO₃ is expressed asCa=0.5TA+0.63NO₃ The values of Ca obtained from direct measurements in the North Pacific are in good agreement with the values estimated from this equation.     

δ15N of PON and Nitrate as a Clue to the Origin and Transformation of Nitrogen in the Subarctic North Pacific and Its Marginal Sea

Nitrogen isotope compositions of particulate organic matter and nitrate were analyzed for seawater sampled at five stations at the Alaskan Gyre, Western Subarctic Gyre and East China Sea, focusing on the samples from the surface to 5000 m water to characterize the nitrogen cycling in the subarctic North Pacific Ocean and its marginal sea. The ¹⁵N of particulate organic matter showed little agreement with a conceptual closed model that interprets isotopic variation as being caused by isotope discrimination on nitrate utilization. The ¹⁵N and ¹³C of particulate organic matter varied with the water depth. A correlation between isotope compositions and C/N elemental ratio was found generally at all stations, although some irregular data were also found in deep layers. We developed a hypothetical nitrogen balance model based on N₂ fixation and denitrification in seawater and attempted to apply it to distinguish nutrient cycling using both ¹⁵N-NO₃ ^– and N* variation in seawater. This model was applied to the observed data set of ¹⁵N-NO₃ ^– and N* in the North Pacific water and estimated the ¹⁵N-NO₃ ^– of primordial nitrate in the North Pacific deep water as 4.8. The North Pacific intermediate water for all stations showed similar ¹⁵N-NO₃ ^– and N* values of 6 and –3 µmol/kg, respectively, suggesting a similar nitrogen biogeochemistry. In the East China Sea, analysis showed evidence of water exchange with the North Pacific intermediate water but a significant influence of nitrogen from the river runoff was found in depths shallower than 400 m.     

Mean Vertical Distribution of the Dissipation Rate of Turbulent Energy in the Black Sea. Comparison with the Existing Models

We compare the results obtained by using theoretical and semiempirical models developed for the evaluation of the dissipation rate of turbulent energy in a stratified ocean with independent distribution of this quantity established by the authors for the active layer of the Black Sea (50–300 m) by using a one-dimensional model taking into account the balance of heat, salt, and fluid inside the layer. It is shown that, in a layer with gradual variation of the Väisälä–Brunt frequency N as a function of depth, the predominant sink of the energy of motion into dissipation N ² is ensured by the flow of energy through the spectrum of internal waves toward low frequencies and small vertical scales. On the contrary, in layers with abrupt drops of density as a function of depth (layers with jumps of density), an important role is played by the interface-type waves and the dependence of on N transforms into N .     

Practical Formulas for Intercoupling of Pressure and Depth in the Black Sea

On the basis of the generalization of the concept of standard ocean to the Black Sea, we deduce practical formulas for the conversion of pressure into depth and vice versa depending on the latitude of the place with regard for the equation of state for 1980. The error of these relations for the standard Black Sea (whose salinity is equal to 22.2 at a temperature of +9°C from the surface to the bottom) does not exceed ±0.2m and ±0.2dbar. The difference between the practical and actual depths in winter and summer periods does not exceed ±0.35m for depths varying within range 0–2000m. The proposed practical formulas enable one to simplify the procedure of rapid evaluation of depth (or pressure) in real time by excluding the procedure of integration over a specific volume.     

Kinetics of nitrate and ammonium uptake by the natural populations of marine phytoplankton in the surface water of the Oyashio region during spring and summer

The maximum uptake rate (_max) and affinity constant (K _s) for nitrate and ammonium were estimated in the surface water of offshore Oyashio in May (spring) and September (summer), 1990. The average _max/Chl.a for ammonium was 2.1 times larger than that of nitrate in both seasons. The average _max/Chl.a for both nitrogens were 3.5 times larger in summer than in spring. Water temperature and size composition of phytoplankton population were related to the seasonal difference in the _max/Chl.a. Phytoplankton population showed high affinity for both nitrogens in the spring and summer. In addition, the contribution of new production to total production was estimated by _max[_max–No₃/(_max–NO₃+_max–NH₄)]. The spring value was in the range of 0.26 to 0.45 (mean±SD=0.35±0.092), and the values in spring bloom were especially a little over 0.4. The summer value was in the range of 0.30 to 0.37 (0.34±0.04).     

Radiation balance and heat budget at the ocean/atmosphere interface in the western North Pacific

The downward short- and long-wave radiation fluxes at the sea surface (S, L) were measured aboard the R/VHakuho Maru, University of Tokyo, for the period of 117 days on six cruises from 1981 to 1985 in the western North Pacific near Japan. The upward fluxes of short- and long-wave radiation (S, L) were calculated by Payne's (1972) table and the Stefan-Boltzmann's law, respectively. The sensible and laten heat fluxes (Q _h ,Q _e ) were also estimated from an aerodynamic bulk method.From April to August, the daily mean value ofS varied with the amplitude of 100200 Wm^–2. The value ofS was estimated approximately 6% ofS in all seasons. The difference betweenL andL was so small that the net radiation flux (Q _n ) was dominated byS. In addition, the net heat flux at the sea surface was also dominated byS due to small values ofQ _h andQ _e , and then the ocean was warmed at the rate of 111 Wm^–2 in April and 63 Wm^–2 in August in the Oyashio Area, and 132 Wm^–2 in May and 164 Wm^–2 in June in the Kuroshio Area, respectively.From September to March, a remarkable negative correlation between the day to day variation ofS and that ofL was observed except when an intense cold air outbreak occurred. It was found that the correlation was caused by the cloud climatological feature of the western North Pacific in this period.S was not a dominant factor in the net heat flux. The value ofQ _h +Q _e in the Kuroshio Area ranged from 260 Wm^–2 to 630 Wm^–2, much larger thanQ _n which ranged from –8 Wm^–2 to 92 Wm^–2 in the leg mean values (each leg period was about 10 days). Then the ocean was cooled at the rate of –160–620 Wm^–2 during this period. The net heat flux in the Kuroshio Area averaged over five legs from late November to February was –473 Wm^–2. This value is 50100% larger than the climatological values reported so far.The temporal and spatial variability of radiation fluxes and heat fluxes during each leg was also discussed.     

Organic geochemistry of the Japan Sea sediments-1: Bulk organic matter and hydrocarbon analyses of Core KH-79-3, C-3 from the Oki Ridge for paleoenvironment assessments

Organic geochemical study of bulk organic matter (OM), hopanoid hydrocarbon and normal hydrocarbon (C₂₃C₃₅) was conducted for a 936-cm-long sediment core sample from the Oki Ridge of the Japan Sea (Core KH-79-3, C-3; 37°03.5 N, 134°42.6E, water depth 935 m). Stable carbon isotopic ratios were also measured for both bulk OM and individual hydrocarbons. The following results were obtained: (1) The weight ratios of total organic carbon to total nitrogen range from 6.2 to 9.4 in the core. The ¹³C values of bulk OM range from –25.1–20.7%.. The ¹³C values of OM in the sections of 140190 cm are lower (–25–24) than those in the other sections (–23–21). This result indicates that OM in the core except for the 140190 cm sections is essentially of marine origin. (2) The ¹³C value of diploptene (a hopanoid hydrocarbon) in the last glacial maximum (LGM), is –66.3 (vs. PDB), which indicates it originating in methanotrophic bacteria. This result provides evidence to support for the previous ideas (Oba et al., 1980, 1984; Masuzawa and Kitano, 1984) that the bottom waters in the Japan Sea were anoxic in LGM. (3) Long chain (C₂₃C₃₅) n-alkanes of higher-plant wax origin were found throughout the core. Their concentration is high in 140190 cm in depth, suggesting that eolian dust load was high in LGM. (4) The n-alkane/TOC ratio increases with decreasing ¹³C values of bulk OM. This result indicates that the load of terrestrial (probably eolian dust-derived) OM to the Japan Sea became higher in colder climates. (5) The CPI values of long-chain n-alkanes are different in different ¹³O stages of paleoclimate, probably reflecting variations in species of terrestrial higher plants as a result of climatological adaptations.     

Regeneration of silicate in the ocean

Regeneration of silicate in the Japan Sea, an example of semi-closed sea, was studied. In the Japan Sea Proper Water the apparent regenerative ratio of the nutrients was determined to be:O C N P Si=–289 (116)14.3181.It was assumed that the dissolved silicate present in sea water is grouped into three fractions; 1)preformed silicate of conservative nature, 2)oxidative silicate which dissolves in oxidation process of organisms with consumption of oxygen, and 3)non-oxidative silicate which dissolves without oxygen consumption. The dissolution rate ofnon-oxidative silicate in the Japan Sea Proper Water was estimated to be 0.07g-at. Si/l/yr from the data ofAOU values and assumed rates of oxygen consumption. This dissolution rate ofnon-oxidative silicate agreed with that obtained in the deep Pacific by the vertical advection diffusion model byKido andNishimura (1972).     

Morphology of largeHalimeda bioherms,eastern Java sea (Indonesia): A side-scan sonar study

The most extensive and thickestHalimeda bioherms reported from modern seas occur along both open and protected margins of Kalukalukuang Bank, eastern Java Sea (Indonesia). Seismic profiles suggest these features average 20 to 30 m thick (maximum 50 m) and developed over large areas by coalescence of individual mounds. Bioherm morphologies range from numerous small mounds ( 10–20 m diameter) through hay-stack features ( 100 m diameter) to broad swells. Some modern bank bioherms display surface forms that appear related to onbank flow from Makassar Strait. Upwelling of cold, nutritive water is likely responsible for unusualHalimeda productivity and large bioherm development.     

Study on the chemical forms of radionuclides in seawater-III complexes of60Co with amino acids

Stability constants were determined for⁶⁰Co (II)-amino acid complexes in sodium perchlorate media at an ionic strength=0.67, using cation exchange resins. Stability constants were, for Co(II)-phenylalanine, log ₁=4.4, log ₂=8.2, log ₃=11.7, for Co(II)-histidine, log ₁=7.4. for Co(II)-valine, log ₁=4.3, log ₂=8.5, for Co(II)-proline, log ₁=4.1, and for Co(II)-tyrosine, log ₁=7.2, respectively. The abundance of Co(II)-amino acid complexes in seawater was calculated from these stability constants on the basis of chemical equilibrium, assuming the concentration of individual amino acid to be 10^–7 to 10^–8 mol l^–1. It was inferred that the Co(II)-amino acid complexes are probably not formed abundantly in seawater while inorganic species of⁶⁰Co(II) may still be dominant for a short period of time after discharge into seawater as liquid waste.     

A stratigraphic and tectonofacies framework of the “calcari aLucina” in the Apennine Chain,Italy

The Apennine Chain provides the first example of stratigraphic (time) and synsedimentary tectonic (space) distribution of the calcari aLucina Miocene equivalents of modern cold-vent carbonates. Chemosynthetic faunal assemblages and related carbonate deposits are found at different stratigraphic levels, with peaks during Langhian-Serravallian and late Tortonian-early Messinian times. A general increase in frequency and volume occurs with time. A genetic link between venting and the Messinian Evaporite event is difficult to demonstrate. However,Lucina limestones are limited to preevaporitic times, and their maximum abundance is reached just before the onset of the Messinian Evaporite accumulation.Lucina limestones occur in almost all tectofacies of the orogen, from backland to foreland.     

Primary productivity in the offshore Oyashio in the spring and summer 1990

Primary productivity was measured byin situ method using¹³C in the offshore Oyashio region in the spring (May) and summer (September) of 1990. Most of the values were within the range of 0.1 to 4 gC 1^–1 h^–1 although a very large value, 7.96 gC l^–1 h^–1, was observed in summer. Most daily primary production fell within the range of 372 to 633 mgC m^–2 d^–1 although a very large value, 2,109 mgC m^–2 d^–1, was observed around the frontal area in summer. Chlorophylla (Chl.a) exceeded 1 g l^–1 in many cases, and the maximum was 4.61 g l^–1 in spring and 7.53 g l^–1 in summer. Most primary productivity per unit Chl.a (photosynthetic assimilation ratio) was within the range of 0.1 to 3 gC gChl.a ^–1 h^–1 although higher values, 3–6 gC gChl.a ^–1 h^–1, were observed where small-size phytoplanktons (<2 m) were dominant. These results were compared with results obtained until now in the Oyashio region. The values beyond the range obtained so far in the offshore region were also observed in this study. Furthermore, it was pointed out that the size composition of phytoplankton community has significant influence on the results of Chl.a and photosynthetic assimilation ratio in the Oyashio region.     

Heat balance of the upper ocean under a land and sea breeze in Sagami Bay in summer

The heat balance of the upper ocean under a land and sea breeze was investigated based on observations of sea water temperature in the upper 300 m layer and heat flux across the sea surface at a fixed station in Sagami Bay (3510N, 13925E) during two periods of two days in August 1980 and three days in August 1981. During both periods, a typical land and sea breeze of 4–6 m sec^–1 at maximum prevailed in the observation area. Large diurnal variation of sea surface temperature with a maximum peak around noon LST was observed during both periods (the daily value of the range was 0.9C and 2.5C in 1980, and 1.2C, 1.5C and 1.7C in 1981). It was found that these large temperature variations were caused by diurnal variation of the wind speed which dropped to 0–3 m sec^–1 at noon when the strongest insolation (–270 Wm^–2) penetrated the sea and at midnight in association with alternations of the land breeze and the sea breeze. On the other hand, vertical mixing of the sea water caused by the wind stress and/or convection due to cooling at night extended down only to the surface 10 m layer. Horizontal heat advection was negligibly small. Therefore the local time change of the heat content in the upper 10 m water column was affected mainly by the heat flux across the air-sea interface which was estimated from data on radiation fluxes measured directly on board and latent and sensible heat fluxes calculated by the aerodynamic bulk method. The water temperature below the 10 m layer also varied with time and the temperature variation in the thermocline (20–50 m depth) was frequently larger than that of the sea surface temperature. However, the variation in the upper 10 m layer was little influenced by that below the layer.     

Rates of net assimilation and respiration of amino acids by marine bacteria

The selectivity of amino acid assimilation by marine bacteria was examined using seven kinds of¹⁴C-amino acids and the acid hydrolysate of¹⁴C-labelled proteins. It was found that the net assimilation and respiration by marine bacteria followed MICHAELIS-MENTEN kinetics for all of amino acids used in our experiments. Maximum velocities of amino acids were 0.01 to 0.19g carbon/hour per 2×10⁷ cells for net assimilation and less than 0.18g carbon/hour per 2×10⁷ cells for respiration at 20C. The velocity of gross assimilation was found with the following order: phenylalanine>valine, glutamic acid>serine, arginine>tryptophan>glycine. The assimilation velocities of amino acids in these laboratory works showed almost the same order as those in field experiments. The assimilation velocity of an amino acid was influenced by coexisting another amino acids or glucose. The assimilation velocity in lower substrate range of amino acids was directly proportional to the number of bacterial cells in the range from 6×10² to 3×10⁴ cells per ml. No linear relation between the assimilation velocity of amino acids and reciprocal of absolute temperature was found, but a marked bending was observed at 15 to 20C. The velocity at the optimum temperature was three to six times of that at 5C.     

Thermolability of dehydrogenases from a psychrophilic marine bacterium

The heat lability of succinic dehydrogenase, malic dehydrogenase and lactate dehydrogenase in cell-free extracts ofVibrio marinus MP-1 grown at 15C was compared for the tris buffer suspended enzymes and the NaCl suspended enzymes. The tris buffer suspended enzymes lost 50 percent activity at low thermal exposure between 5C and 27C. No activity was evident on thermal exposure between 32C and 39C. The enzyme extracts suspended in NaCl at 36 % were more heat stable, losing 50 percent activity after exposure between 16C and 40C. The enzymes lost all activity on thermal exposure between 33C and 42C in the presence of NaCl.     

A field study of physico-chemical states of artificial radionuclides in seawater

The physico-chemical states of artificial radionuclides,⁹⁰Sr,¹³⁷Cs and¹⁴⁴Ce in seawater were investigated by radiochemical analysis of filtered and unfiltered seawater. The difference of radionuclide concentrations between unfiltered and filtered seawaters was defined as the particulate form radioisotope and its particle ratio was discussed.Practically no particulate⁹⁰Sr, greater than 0.22 in size, was observed in both coastal and open seawaters, but some of¹³⁷Cs seemed to be insoluble in some circumstances, especially in coastal waters. A considerable amount of¹⁴⁴Ce was found to be particulate.An estimation of the radionuclides in particulate form was made for Kashima-nada seawaters collected in 1970 to 1972, and it was shown that the possible occurrence of particulate radionuclides, greater than 0.22 in size, were 1% or less for⁹⁰Sr and 6% for¹³⁷Cs. In the coastal water, 80 % of¹⁴⁴Ce were seemed to be in particulate form, but in the open seawater only a few%. The influences of suspended materials to¹³⁷Cs and¹⁴⁴Ce concentration levels in seawater were not negligible and further investigations are desirable.