Some features of jump in water temperature in aSargassum forest

To clarify the influence of aSargassum forest on water temperature distributions observations were made inside and outside aSargassum forest off the Nagata Shore on the northern Saiki Bay open to the Bungo Channel on the Pacific side of Kyushu, Japan. About sixty thermistor probes were deployed at 0.5 m depth intervals from the bottom to the sea surface at seven stations spaced at 50–80 m distances along two transects: one inside the forest and the other outside. Water temperature was measured at five minutes intervals from 6 to 9 August 1987 with thermistor probes. The spatial standing crop distribution of theSargassum forest along the transects was investigated. A water temperature jump of about 2°C, recorded during the observation, is probably caused by an intrusion of a warm water mass from the central Bungo Channel to Saiki Bay. The water temperature jump under theSargassum forest on the rough bottom with stones occurred one to two hours behind that outside the forest (sandy bed) although the distance between the transects inside and outside the forest was only 50–80 m. It is suggested that theSargassum forest and the rough bottom would prevent intruding warm water from smoothly replacing cold water due to resistance of theSargassum species and the bottom to a current.     

Standing stocks and production rates of phytoplankton and planktonic copepods in the Inland Sea of Japan

Standing stocks and production rates of phytoplankton and planktonic copepods were investigated at 15 stations in the Inland Sea of Japan during four cruises in October–November 1979, January, April and June 1980. The overall mean of phytoplankton biomass was relatively constant during the study period, ranging from 2.3 mg chl.a m^–3 in April to 3.6 mg chl.a m^–3 in October–November. Primary production was low in January (mean: 90 mg C m^–2 d^–1), but higher than 375 mg C m^–2 d^–1 on the other occasions. Integrated annual primary production was 122 g C m^–2 yr^–1. In terms of carbon weight,Paracalanus parvus was the most important copepod species. The variation of the mean copepod biomass (range: 7.6 mg C m^–3 in April to 20.2 mg C m^–3 in June) was smaller than that of copepod production, which was estimated by the Ikeda-Motoda's physiological method. Copepod producion was low in cold seasons (0.6 and 0.9 mg C m^–3 d^–1 in January and April, respectively), and increased, following the elevation of primary production, to 4.9 mg C m^–3 d^–1 in June. Annual copepod production was 33.7 g C m^–2 yr^–1, of which herbivore (secondary) production was 26.4 g C m^–2 yr^–1 (21.7% of primary production). The ratios of pelagic planktivorous fish catch and total fish catch to the primary production were 0.82 and 1.8%, respectively, indicating very high efficiency in exploiting fishery resources in the Inland Sea of Japan.     

Evapotranspiration from citrus trees growing in sandy soilunder drip irrigation with saline water

An experiment on evapotranspiration from citrus trees under irrigation with saline waterwas carried out for 4 months. Two lysimeters planted with a citrus tree in the green house wereused. One lysimeter was irrigated with saline water (NaCl and CaCl2 of 2000 mg/L equivalence,EC = 3.8 dS/m, SAR = 5.9) and the other was irrigated with freshwater using drip irrigation. Theapplied irrigation water was 1.2 times that of the evapotranspiration on the previous day.Evapotranspiration was calculated as the change in lysimeter weight recorded every 30 minutes.The lysimeters were filled with soil with 95.8% sand. The results of the experiment were as follows.(i) The evapotranspiration from citrus tree was reduced after irrigation with saline water. Theevapotranspiration returns to normal after leaching. However it takes months to exhaust the saltfrom the tree. ( ii ) To estimate the impact of irrigation with saline water on the evapotranspirationfrom citrus trees, the reduction coefficient due to salt stress (Ks) was used in this experiment.Evapotranspiration under irrigation with saline water (ETs) can be calculated from evapotranspira-tion under irrigation with freshwater (ET) by the equation ETs = Ks× ET. Ks can be expressed as afunction of ECsw. (iii) The critical soil-water electrical conductivity (ECsw) is 9.5 dS/m, beyondwhich adverse effects on evapotranspiration begin to appear. If ECsw can be controlled at below9.5 dS/m, saline water can be safely used for irrigation.     

Diagnosis of earth-fill dams by synthesised approach of sounding and surface wave method

The spatial distribution of the strength inside the earth-fill is identified by the sounding tests. In this research, the Swedish weight sounding (SWS) is employed, and the spatial high-density test is performed to identify the spatial correlation structure. Furthermore, the synthesised approach of the SWS and surface wave method, which is one of the geophysical method, is proposed to compensate the shortage of each approach. Consequently, the correlation structure of an earth-fill could be identified accurately, and the high resolution of the spatial distribution could be visualised based on the survey results.     

Changes in the abundance and composition of picophytoplankton in relation to the occurrence of a Kyucho and a bottom intrusion in the Bungo Channel,Japan

The Bungo Channel in southwestern Japan receives both warm, called Kyucho, and cold deep-water intrusions (bottom intrusion) from the Pacific Ocean. Abundances of Prochlorococcus, Synechococcus, and eukaryotic picophytoplankton were monitored from 18 July to 17 August 2001 to clarify whether advected picophytoplankton from the Pacific Ocean can grow in the channel or not. Synechococcus cells were further discriminated into low- and high-PUB types according to their fluorescence property in flow cytometry. From 18 to 25 July, the water temperature decreased by 3 °C at a 5-m depth at all stations, indicating the occurrence of a bottom intrusion. From 25 July to 4 August, a Kyucho occurred and the water temperature rapidly increased. From 4 to 17 August, a bottom intrusion and a Kyucho both occurred twice, although the intensities were smaller than those occurring until 4 August. From 18 to 30 July, the abundance of both Prochlorococcus and a high-PUB type of Synechococcus drastically decreased because of a bottom intrusion; however, the abundances rapidly increased due to the advection by a Kyucho. These advected cells increased from 4 to 17 August in the channel and Kitanada Bay. Changes in the abundance of low-PUB type of Synechococcus and eukaryotic picophytoplankton were less noticeable than those in the abundance of Prochlorococcus and high-PUB type. The present study demonstrated that oceanic picophytoplankton advected by the Kyucho could grow in the channel. However, abundances of low-PUB type and eukaryotic picophytoplankton increased higher than those of Prochlorococcus and high-PUB type did. Thus, these oceanic phytoplankters will be excluded when Kyucho does not occur for a long time. The co-occurrence of various types of picophytoplankton found in the channel is probably achieved by both Kyucho event and their growth capability in the channel.     

Human and climate forcing of zooplankton populations: Introduction

Zooplankton play a key role in the pelagic foodweb by controllingphytoplankton production and shaping pelagic ecosystems. Inaddition, because of their critical role as a food source forlarval and juvenile fish, the dynamics of zooplankton populationshave a significant influence on recruitment to fish stocks.In 1961, ICES convened the First Zooplankton Production Symposiumin Charlottenlund, Denmark. ICES also played a leading rolein the Second Zooplankton Production Symposium on "ZooplanktonProduction: measurement and role in global     

Length-weight relationships of important zooplankton from the Inland Sea of Japan

Measurements of dry weight, carbon- and nitrogen contents together with the body length of important zooplankton from the Inland Sea of Japan were made using freshly caught specimens. The values of the former three parameters were found to be highly correlated to length, and species specific regression equations were calculated for 10 species of Copepoda (Calanus sinicus, Euchaeta plana, E. concinna, Centropages abdominalis, Sinocalanus tenellus, Acartia clausi, A. tsuensis, Tortanus forcipatus, Oithona brevicornis andO. similis), 3 species of Cladocera (Podon leuckarti, P. polyphemoides andPenilia avirostris), 1 species of each of Mysidacea (Neomysis japonica), and Natantia (Acetes japonicus), and two forms of Chaetognatha (Sagitta crassa andS. crassa f.naikaiensis).     

Chemical gradient at diffusive interfaces in magma chambers

The results of high pressure experiments on diffusion and Soret separation in natural silicate melts show that the diffusive behaviour between natural silicic and mafic magmas can be approximately modelled as if the system were a binary mixture of SiO₂ and other components such as MgO+FeO+CaO. Steady state compositional profiles across a diffusive interface between silicic and mafic magma layers are calculated on the basis of phenomenological relationships for the fluxes of chemical species and heat in the binary mixtures, using the experimental data of diffusion and Soret coefficients in natural silicate melts. The compositional profiles show a curvature with a minimum SiO₂ value within the interface due to the Soret effect and temperature dependence of diffusion coefficient. The compositional gradient at the lower half of the diffusive interface is similar to that resulting from the Soret separation of a mafic melt regardless of the composition of the silicic magmas. These results suggest that picritic magma can be formed in the interfacial region between the mafic and silicic magma layers. The compositional gradient explains chemical variation of mafic to picritic inclusions in a mixed andesite of the Abu Volcano Group, Japan.     

Space-time distribution patterns of destructive earthquakes in the inner belt of central Japan: Activity intervals and locations of earthquakes

Based on a block structure model of the inner belt of central Japan, an examination was conducted of the space-time distribution patterns of destructiv magnitudes M 6.4 or greater (M =Japan Meteorological Agency Scale). The distribution patterns revealed a periodicity in earthquake activit seismic gaps. Major NW—SE trending left-lateral active faults divide the inner belt of central Japan into four blocks, 20–80 km wide. The occurrenc A.D. with M ≥ 6.4, which have caused significant damage, were documented in the inner belt of central Japan. The epicenters of these earthquakes close to the block boundaries.

Using the relationship between the magnitude of earthquakes which occurred in the Japanese Islands and the active length of faults that generated them, movement is calculated for each historical earthquake. Space—time distributions of earthquakes were obtained from the calculated lengths, the latitud of generation. When an active period begins, a portion or segment of the block boundary creates an earthquake, which in turn appears on the ground surf active period ends when the block boundary generates earthquakes over the entire length of the block boundary without overlapping.

Five seismic gaps with fault lengths of 20 km or longer can be found in the inner belt of central Japan. It is predicted that the gaps will generate ea magnitudes of 7.0. These data are of significance for estimating a regional earthquake risk over central Japan in the design of large earthquake resist

The time sequences of earthquakes on the block boundaries reveal a similar tendency, with alternating active periods with seismic activity and quiet pe activity. The inner belt of central Japan is now in the last stage of an active period. The next active period is predicted to occur around 2500 A.D.     

Life-time of a stratified magma chamber recorded in ultramafic xenoliths from Ichinomegata volcano,northeastern Japan

Variations in major-element chemistry and modal compositions of the mantle xenolith-bearing calc-alkalic ejecta from Ichinomegata volcano are inferred to be due to mixing of three magmatic end members: Basalt I (SiO₂ 51 wt% , MgO 8.5 wt%), Basalt II (SiO₂ 54 wt%, MgO 5 wt%), and Dacite (SiO₂ 65 wt%, MgO₂ wt%). Ultramafic xenoliths are found in mafic mixtures of Dacite-Basalt I and Dacite-Basalt II. The thermal histories of the xenoliths in both mixtures are compared with each other. Chemical compositions of olivine and orthopyroxene in xenoliths suggest that xenoliths in Basalt I were equilibrated at about 800 °C, while those in Basalt II were also equilibrated originally at about 800 °C but were subsequently annealed at about 1000 °C for more than 10^2–3 years prior to the eruption.The chemical composition of Basalt I indicates that it can coexist with upper mantle peridotite and it is an appropriate candidate for a carrier of ultramafic xenoliths from the upper mantle. On the other hand, Basalt II is fractionated and it cannot be directly derived from the upper mantle. Two pulses of xenolith-bearing basalt injection into a dacite magma chamber are inferred to have occurred. The first injection did not lead to eruption and subsequently formed a dacite/basalt stratified magma chamber. In the lower layer, the basalt was slightly differentiated to become Basalt II and ultramafic xenoliths carried by the first pulse were annealed at the bottom of the layer. The duration of the annealing of the xenoliths implies a minimum life-time of the Dacite-Basalt II stratification in the magma chamber beneath Ichinomegata of 10^2–3 years. The second injection of the xenolith-bearing basalt (Basalt I) was immediately followed by eruption, and all the magmas were effused with mixing in a conduit. Consequently, the ultramafic xenoliths carried by the second pulse are not annealed.