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61.
石灰性土壤上植物根际中Fe,Mn的形态分布及其与植物吸收的关系 总被引:2,自引:1,他引:1
研究了石灰性土壤上5种作物品种根际微生态环境中Fe、Mn的形态分布.结果表明,交换态Fe(EX-Fe)、碳酸盐结合态Fe(CARB-Fe)、无定形氧化铁(AO-Fe)和交换态Mn(E-Mn)、碳酸盐结合态Mn(CARB-Mn)在根际土壤中都呈现明显的累积.各品种根际中的累积量有较大差异.相关分析表明,黄潮土上植株含Fe量、吸Fe量与根际土壤AO-Fe含量呈显著正相关.根际有效态Fe累积不仅是根际pH作用的结果,与根系分泌物对难溶性Fe活化有关.根际有效态Mn累积则受到根际土壤Eh的影响. 相似文献
62.
Elena Driomina Igor Polnikov Victor Sharov Ofelia Azizova Yury Vladimirov 《Free radical research》1994,20(5):279-288
A chemiluminescence (CL) flash kinetics on the addition of Fe2+ ions into oxidized low density lipoprotein (LDL) suspension has been studied. LDL oxidation was carried out at 37°C without and in the presence of 5 or 50 μM of Cu.2+ It has been found that under certain experimental conditions (the addition of excess iron ions, more than 1 mM) the amplitude of CL flash depended almost linearly (1) on the concentration of oxidized LDL and (2) on the extent of LDL oxidation measured as diene conjugates (DC) and 2-thiobarbituric acid-reactive substance (TBARS) accumulation. The corresponding correlation coefficients were: for TBARS - 0.94 and for DC - 0.97, in the case of LDL autooxidation; 0.72 and 0.98, in the case of copper-induced LDL oxidation. A sensitivity of the CL method was shown to be significantly enhanced (by more than two orders) in the presence of CL sensitizer - 2, 3,5, 6-lH,4H-tetrahydro-9-(2' -benzoimidazolyl)-quinolizin-(9, 9a, 1 -gh)coumarin. 相似文献
63.
This article concerns seasonal variations in the phosphate concentrations in two coastal lagoons near Montpellier (Mediterranean
coast, France). The o-P concentration in the overlying water is highest during summer. The role of the sediment, particularly
that of the different P fractions in the sediment, is discussed. Significant variations, especially in the FeOOH ≈ P fraction,
occur. For both Tot-Psed and the Fe00H≈P fraction a gradient from surface to bottom is observed, as well as a distinct decrease in the FeOOH≈P fraction
in the surface sediments during summer and autumn. Variations in the FeOOH≈P fraction appear to be compensated by variations
in the CaC03≈P fraction. These variations appear to be determined by the ferric hydroxide concentration. This compound represents only
a small part (maximally 15%) of the total iron in the sediments and is related to the dissolved oxygen content of the immediately
overlying water. Besides the fractions o-P, Fe(OOH)≈P, a large part of the CaC03≈P fraction is potentially bioavailable. A large proportion of the Tot-Psed is therefore bioavailable.[/p] 相似文献
64.
The purpose of this study was to make a prognosis of the effects of extended purification of terrestrial waste water, reaching the Wadden Sea by the River Rhine and Lake IJssel, on the phosphate concentration in the western Wadden Sea.The quantities of different phosphorus fractions in intertidal and subtidal sediments of the Marsdiep tidal basin (western Dutch Wadden Sea) were measured. Different methods are applied to determine the amount of phosphorus that can be released from these sediments. The direct bioavailability is determined by inoculating sediment suspensions with a natural mixture of precultured micro-organisms from the sampling area. A second approach is the measurement of the phosphate release under different redox conditions. Sequential extraction of sediment samples with different solvents is also applied. Under the present conditions and compared to the nutrient loads from fresh water (Lake IJssel) and from the North Sea, the phosphorus stored in the sediments of the western Dutch Wadden Sea plays a minor role in the total supply to micro-algae and bacteria. The bulk of the biologically available phosphorus in the sediments originates from the metal-associated fraction. Releasable phosphate may contribute to the local annual primary production to an extent of ca 45 to ca 150 g C m–2 a–1. The total amount of phosphorus in the sediment (mainly calcite associated) is twice to 6 times the biologically available amount. 相似文献
65.
Iron content of sediment and phosphate adsorption properties 总被引:9,自引:2,他引:7
Phosphorus can occur in sediments in different forms and accordingly its availability varies. The distinction between the phosphorus fractions is made with two chemical extraction methods; an ammonium oxalate-oxalic acid extraction and an extraction according to Hieltjes & Lijklema (1980).The iron and aluminum liberated with the ammonium oxalate-oxalic acid extraction method is linearly correlated (r
2 = 0.73) with the phosphorus liberated in the first two steps of the Hieltjes and Lijklema extraction by: P = 0.035 (Fe + Al) + 0.001 (P, Fe and Al in mmol g–1).The iron and aluminum (hydr)oxides are very important fractions in the sediment adsorption capacity for phosphorus. The phosphorus sorption capacity (PSC) is 0.080 mol P (mol (Fe + Al))–1 and the adsorption constant (k) is 11.9 µmol P l–1. Here it is assumed that iron and aluminum (hydr)oxide have the same affinity for phosphorus. 相似文献
66.
67.
The role of mineral compounds and chemical conditions in the binding of phosphate in the Ems estuary
In the Ems estuary the gradients in dissolved phosphorus and iron are non-conservative and opposite. The relations between
different mineral compounds, environmental conditions and phosphate concentrations were studied, in an attempt to explain
this. Laboratory experiments on water samples from the reaches with high concentrations of phosphate and of suspended matter
revealed a low concentration of calcite-bound phosphorus in the middle reaches of the estuary (only 0.07%). Therefore, it
is concluded that calcite possibly plays only a modest role in phosphate distribution in the Ems estuary. Further experiments
revealed that nearly 70% of the particulate inorganic phosphorus is iron-bound. It is demonstrated that organic coatings on
minerals inhibit phosphate release at a low redox potential. Moreover, the organic matter itself contained c. 20% of particulate
phosphorus. Approximately 10% of the particulate phosphorus may be associated with clay minerals. It is concluded that in
addition to biological processes, the phosphorus associated with ironoxyhydroxides may be crucial for the seasonal variation
of the phosphate concentrations in the water. 相似文献
68.
69.
Ferric reductase enzymes requiring a reductant for maximal activity were purified from the cytoplasmic and periplasmic fractions of avirulent and virulent Legionella pneumophila. The cytoplasmic and periplasmic enzymes are inhibited by zinc sulfate, constitutive and active under aerobic or anaerobic conditions. However, the periplasmic and cytoplasmic reductases are two distinct enzymes as shown by their molecular weights, specific activities, reductant specificities and other characteristics. The molecular weights of the cytoplasmic and periplasmic ferric reductases are approximately 38 and 25 kDa, respectively. The periplasmic reductase (K
m = 7.0 m) has a greater specific activity and twice the affinity for ferric citrate as the cytoplasmic enzyme (K
m = 15.3 m). Glutathione serves as the optimum reductant for the periplasmic reductase, but is inactive for the cytoplasmic enzyme. In contrast, NADPH is the optimum reductant for the cytoplasmic enzyme. Ferric reductases of avirulent cells show a 2-fold increase in their activities when NADPH is used as a reductant in comparison with NADH. In contrast, ferric reductases from virulent cells demonstrated an equivalent activity with NADH or NADPH as reductants. With the exception of their response to NADPH, the ferric reductase at each respective location appears to be similar for avirulent and virulent cells. 相似文献
70.
Holger Stephan Stefan Freund Werner Beck Günther Jung Jean-Marie Meyer Günther Winkelmann 《Biometals》1993,6(2):93-100
Novel linear hydroxamate/hydroxycarboxylate siderophores from strains of Pseudomonas cepacia were isolated and named ornibactins. The ornibactins represent modified tetrapeptide siderophores, possessing the sequence l-Orn1(N
-OH, N
-acyl)-d-threo-Asp(-OH)-l-Ser-l-Orn4(N
-OH, N
-formyl)-1,4-diaminobutane. The N
-acyl groups of Orn1(N
-OH, N
-acyl) may vary and represent the three acids 3-hydroxybutanoic acid, 3-hydroxyhexanoic acid and 3-hydroxyoctanoic acid, leading to a mixture of three different ornibactins, designated according to their acyl chain length as ornibactin-C4, ornibactin-C6 and ornibactin-C8. Each of the siderophores is accompanied by a small amount of a more hydrophilic component with a 16 a.m.u. higher mass. The structure elucidation was based on results from gas chromatography amino acid analysis, electrospray mass spectrometry, and one- and two-dimensional nuclear magnetic resonance techniques. 相似文献