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1 ransport the soluble precursor of biosilica, silicic acid.
2 DEAE-cellulose, C18 reverse phase resin, and silicic acid.
3 ial in Sargasso Sea sediments indicates that silicic acid, a limiting nutrient today, may have been m
4 rned holographic structures are exposed to a silicic acid, an ordered array of silica nanospheres is
5 ty over large areas of the EEP is limited by silicic acid and iron availability, and because of this
8 we make use of the combined distributions of silicic acid and nitrate to trace the main nutrient retu
9 teins that bind to a soluble form of silica, silicic acid, and transport it across the cell membrane
10 ns above and below the "mononuclear wall" of silicic acid at 2 x 10(-3) M (where silicic acid is expe
11 silica-rich colloids in solutions containing silicic acid at concentrations of both the regions above
12 tantial increase in the condensation rate of silicic acids by guiding them to form a silicate trimer
13 NO2 that was purified by solvent extraction, silicic acid chromatography, and reverse-phase HPLC.
14 able and eluted with acetone and methanol in silicic acid chromatography, consistent with being a pol
16 s minimized, the hydrophilic and nonvolatile silicic acid components replace water maintaining a flui
19 se photosynthetic protists take up dissolved silicic acid from the water and precipitate opaline sili
20 an 800 microM solution of 96% 29Si-enriched silicic acid, H4SiO4 (pH approximately 8), with a signal
21 "soil solution," contains silicon, mainly as silicic acid, H4SiO4, at 0.1-0.6 mM--concentrations on t
22 xes was achieved using a rapid and sensitive silicic acid HPLC method combined with digital analysis
23 with high silicic acid in the south and low silicic acid in the north, where diatom growth may be li
24 rentially expressed between waters with high silicic acid in the south and low silicic acid in the no
28 ion, occurs by condensation of water-soluble silicic acid proximally to biomolecular interfaces throu
29 ated with a superior competitive ability for silicic acid relative to other siliceous plankton such a
31 reactants, an aluminium hydroxide dimer and silicic acid, second, the reaction products, two distinc
32 al controls on the biogeochemical cycling of silicic acid [Si(OH)4] on the west Antarctica Peninsula
35 erent water depths to demonstrate changes in silicic acid supply and utilization during the most rece
36 By 17 ka, stratification reduced the surface silicic acid supply leading to increased Si utilization
39 efits to many plant species when absorbed as silicic acid through nodulin 26-like intrinsic proteins
41 n which diatoms and radiolarians compete for silicic acid to show that the observed reduction in the
43 .5-18 ka), wind-driven upwelling replenished silicic acid to the subsurface, resulting in low Si util
48 we identify experimentally tractable diatom silicic acid transporter (SIT) homologues and study thei
49 Because all glycosides fail to react with silicic acid under these conditions, reaction appears to
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