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41.
The Algal Growth Potential (AGP) of water samples collected off Gamagori in Mikawa Bay was measured from May 1978 through February 1979, and the limiting nutrient was determined using regression analysis and enrichment bioassays. The surface and bottom water samples had AGP that produced increments of chemical oxygen demand (COD) of 2.1 mg l–1 and 3.1 mg l–1, respectively, on average. These values ofCOD correspond to 46% and 97% of the average COD values of the raw water samples at the surface and bottom, respectively. Seasonal changes of AGP showed a close correlation with those of dissolved inorganic nitrogen (DIN) concentration. Enrichment bioassays showed that DIN was the most deficient nutrient. The DIN:phosphate-phosphorus (PO4
3–-P) ratios and DIN: dissolved phosphorus (DP) ratios in the water samples were below the cellular N:P ratios of the natural algal populations. These results suggest that AGP was mainly limited by DIN concentration. 相似文献
42.
Takemitsu?ArakakiEmail author Hiroyuki?Fujimura Asha?Mansour?Hamdun Kouichirou?Okada Hiroaki?Kondo Tamotsu?Oomori Akira?Tanahara Hatsuo?Taira 《Journal of Oceanography》2005,61(3):561-568
The northern part of Okinawa Island suffers from red soil pollution—runoff of red soil into coastal seawater—which damages coastal ecosystems and scenery. To elucidate the impacts of red soil pollution on the oxidizing power of seawater, hydrogen peroxide (HOOH) and iron species including Fe(II) and total iron (Fe(tot), defined as the sum of Fe(II) and Fe(III)) were measured simultaneously in seawater from Taira Bay (red-soil-polluted sea) and Sesoko Island (unpolluted sea), off the northern part of Okinawa Island, Japan. We performed simultaneous measurements of HOOH and Fe(II) because the reaction between HOOH and Fe(II) forms hydroxyl radical (•OH), the most potent environmental oxidant. Gas-phase HOOH concentrations were also measured to better understand the sources of HOOH in seawater. Both HOOH and Fe(II) in seawater showed a clear diurnal variation, i.e. higher in the daytime and lower at night, while Fe(tot) concentrations were relatively constant throughout the sampling period. Fe(II) and Fe(tot) concentrations were approximately 58% and 19% higher in red-soil-polluted seawater than in unpolluted seawater. Gas-phase HOOH and seawater HOOH concentrations were comparable at both sampling sites, ranging from 1.4 to 5.4 ppbv in air and 30 to 160 nM in seawater. Since Fe(II) concentrations were higher in red-soil-polluted seawater while concentrations of HOOH were similar, •OH would form faster in red-soil-polluted seawater than in unpolluted seawater. Since the major scavenger of •OH, Br−, is expected to have similar concentrations at both sites, red-soil-polluted seawater is expected to have higher steady-state •OH concentrations. 相似文献
43.
When river water mixes with sea water in estuary area, the concentrations of the dissolved element in river water may be changed
by either a simple physical mixing process or some complex chemical processes. It has been clarified in the Chikugogawa River
estuary area that the change in concentrations of SO
4
2−
, BO
3
3−
, Mg2+, Ca2+ and F− is only due to the mixing process but the change in concentrations of SiO
3
2−
and Al3+ is due to the chemical process in addition to the mixing process.
相似文献
44.
45.
Hidetoshi Asanuma Eiji Ohtani Takeshi Sakai Hidenori Terasaki Seiji Kamada Tadashi Kondo Takumi Kikegawa 《Physics and Chemistry of Minerals》2010,37(6):353-359
The melting temperature of Fe–18 wt% Si alloy was determined up to 119 GPa based on a change of laser heating efficiency and
the texture of the recovered samples in the laser-heated diamond anvil cell experiments. We have also investigated the subsolidus
phase relations of Fe–18 wt% Si alloy by the in-situ X-ray diffraction method and confirmed that the bcc phase is stable at
least up to 57 GPa and high temperature. The melting curve of the alloy was fitted by the Simon’s equation, P(GPa)/a = (T
m(K)/T
0)
c
, with parameters, T
0 = 1,473 K, a = 3.5 ± 1.1 GPa, and c = 4.5 ± 0.4. The melting temperature of bcc Fe–18 wt% Si alloy is comparable with that of pure iron in the pressure range
of this work. The melting temperature of Fe–18 wt% Si alloy is estimated to be 3,300–3,500 K at 135 GPa, and 4,000–4,200 K
at around 330 GPa, which may provide the lower bound of the temperatures at the core–mantle boundary and the inner core–outer
core boundary if the light element in the core is silicon. 相似文献
46.
47.
A simple parameterization is proposed to obtain longwave radiative cooling rates, which can be used for atmospheric boundary-layer simulations on clear days in mid-latitudes. The net flux difference which is set to zero at the surface, can be parameterized with the use of three variables: the surface temperature, the lowest level (1.5 m) air temperature, and the total amount of water vapor. If these three elements, along with the water vapor profile are known, it is possible to estimate the cooling rate due to longwave radiation. The results of this parameterization are in good agreement with those of a precise scheme (Roach and Slingo, 1979), within a range of ± 1°C/day of diurnal change for boundary-layer simulations. 相似文献
48.
S. Urakawa T. Kondo N. Igawa O. Shimomura H. Ohno 《Physics and Chemistry of Minerals》1994,21(6):387-391
In situ X-ray diffraction study on KAlSi3O8 has been performed using the cubic type high pressure apparatus, MAX90, combined with synchrotron radiation. We determined the phase relations of sanidine, the wadeite-type K2Si4O9+kyanite (Al2SiO5)+coesite (SiO2) assemblage, and hollandite-type KAlSi3O8, including melting temperatures of potassic phases, up to 11 GPa. Our data on subsolidus phase boundaries are close to the recent data of Yagi and Akaogi (1991). Melting relations of sanidine are consistent with the low pressure data of Lindsley (1966). The breakdown of sanidine into three phases reduces melting temperature, and wadeite-type K2Si4O9 melts first around 1500° C in three phase coexisting region. Melting point of hollandite-type KAlSi3O8 is between 1700° C and 1800° C at 11 GPa. If these potassic phases host potassium in the earth's mantle, the true mantle solidus temperature will be much lower than the reported dry solidus temperature of peridotite. 相似文献
49.
50.
N.?HiraoEmail author E.?Ohtani T.?Kondo T.?Kikegawa 《Physics and Chemistry of Minerals》2004,31(6):329-336
The stability and pressure–volume equation of state of iron–silicon alloys, Fe-8.7 wt% Si and Fe-17.8 wt% Si, have been investigated using diamond-anvil cell techniques up to 196 and 124 GPa, respectively. Angular–dispersive X-ray diffractions of iron–silicon alloys were measured at room temperature using monochromatic synchrotron radiation and an imaging plate (IP). A bcc–Fe-8.7 wt% Si transformed to hcp structure at around 1636 GPa. The high-pressure phase of Fe-8.7 wt% Si with hexagonal close-packed (hcp) structure was found to be stable up to 196 GPa and no phase transition of bcc–Fe-17.8 wt% Si was observed up to 124 GPa. The pressure–volume data were fitted to a third-order Birch–Murnaghan equation of state (BM EOS) with zero–pressure parameters: V0=22.2(8) Å3, K0=198(9) GPa, and K0=4.7(3) for hcp–Fe-8.7 wt% Si and V0=179.41(45) Å3, K0=207(15) GPa and K0=5.1(6) for Fe-17.8 wt% Si. The density and bulk sound velocity of hcp–Fe-8.7 wt% Si indicate that the inner core could contain 3–5 wt% Si. 相似文献