HCO_3~-对不同基因型水稻根生长及养分吸收分配的影响

采用营养液培养法 ,研究了缺Zn敏感 (IR2 6)和耐性水稻品种 (IR8192 31 2 )根生长和养分吸收受HCO-3影响的差异 .结果表明 ,HCO-3( 2 0mmol·L-1)严重抑制敏感品种根系生长 ,特别是在低Zn或缺Zn条件下 ,而对耐性品种影响很小 ,在低Zn水平下 ,对根系生长甚至有轻微的促进作用 .HCO-3不仅抑制敏感品种对Zn的吸收和分配 ,而且也抑制对Cu、Mn和Fe的吸收 ,表明HCO-3对Zn的吸收无专性抑制作用 ,HCO-3抑制敏感品种根系生长可能是其诱发缺Zn的最初作用 .HCO-3处理下 ,耐性品种上位叶和下位叶Zn浓度以及比率高于敏感品种 ,表明耐性品种将Zn从下位叶向上位叶转运的效率高 ,Zn在植物体内的转运能力可能是耐性品种适应石灰性土壤缺Zn的主要机制之一 .     

HCO3-对不同基因型水稻根生长及养分吸收分配的影响

采用营养液培养法,研究了缺Zn敏感(IR26)和耐性水稻品种(IR8192-31-2)根生长和养分吸收受HCO₃^-影响的差异.结果表明,HCO₃^-(20mmol·L^-1)严重抑制敏感品种根系生长,特别是在低Zn或缺Zn条件下,而对耐性品种影响很小,在低Zn水平下,对根系生长甚至有轻微的促进作用.HCO₃^-不仅抑制敏感品种对Zn的吸收和分配,而且也抑制对Cu、Mn和Fe的吸收,表明HCO₃^-对Zn的吸收无专性抑制作用,HCO₃^-抑制敏感品种根系生长可能是其诱发缺Zn的最初作用.NCO₃^-处理下,耐性品种上位叶和下位叶Zn浓度以及比率高于敏感品种,表明耐性品种将Zn从下位叶向上位叶转运的效率高,Zn在植物体内的转运能力可能是耐性品种适应石灰性土壤缺Zn的主要机制之一.     

硝态氮（NO3^—）对水稻侧根生长及其氮吸收的影响

侧根是植物吸收利用土壤养分的重要器官 ,其生长发育受内部遗传因子和外部环境矿质养分的影响。通过琼脂分层培养发现 :局部供应NO-3 可以诱导水稻 (OryzasativaL .)主根或不定根上侧根的生长。为研究旱种条件下NO-3 对水稻侧根发育及其N吸收的影响 ,设置了 3个蛭石培养实验 :分根处理、全株缺N、全株供N处理。分根处理 (一半根系供应 3mmol/LKNO3,另一半根系供应 3mmol/LKCl)结果表明 :局部供应NO-3 能够促进水稻侧根生长。而在全株处理下 ,N饥饿诱导了侧根的伸长。水稻根系对NO-3 的这两种反应都存在着显著的基因型差异。同时对地上部N浓度、可溶性总糖含量及N含量分析表明 ,这些生理指标在分根处理与全株加N处理中的差异均不显著 ,表明分根处理也能基本满足植株正常生长对N的需求。在分根处理中 ,水稻的N含量与分根处理中供N一侧的平均侧根长度存在显著正相关 ,这表明在养分不均一的介质中 ,侧根长度对水稻N素吸收具有十分重要的作用。而在N素充足的条件下 ,两者之间的相关性并不显著 ,这暗示在养分充足的环境下 ,侧根长度可能并不是决定根系吸收N素的主要因素     

低磷胁迫对水稻苗期侧根生长及养分吸收的影响

用蛭石与石英砂作为混合培养介质研究了低磷胁迫对水稻（Oryza sativa L.)苗期侧根发生发育的影响及其与磷吸收的相关关系。结果表明：低磷对水稻的侧根发生发育具有明显的诱导作用及基因型差异。相关性分析表明：单位侧根长度的增加与单位根表面积的增大极显相关,而单位侧根数量的增多与单位根表面积的增大无显的相关性。表明单位根表面积的增加主要来自于单位侧根的伸长。侧根参数与磷含量的相关性分析表明：低磷条件下,侧根总长度和侧根数量都与植株磷含量存在显的正相关,根系总表面积与磷含量存在极显的正相关。表明在低磷条件下,侧根的发生发育对水稻的磷吸收具有重要的作用。根系和地上部的可溶性糖含量分析表明;低磷胁迫改变了同化物在地上部和根系的分配。生物量测定表明：低磷胁迫显增大了植株的根冠比。     

氮肥对夏秋季茶树吸收根生物量和养分储量的影响

以12年生龙井43茶树为研究对象,在7月至翌年1月利用土钻法对连续5a施用不同氮肥处理后的茶树吸收根生物量和养分含量进行了研究。结果表明茶树吸收根生物量在0.34-0.72 mg/dm3之间,碳、氮、磷、钾和镁储量变异范围分别为12.6-25.2 mg/dm~3、4.55-11.2 mg/dm~3、0.47-1.19 mg/dm~3、1.31-4.05 mg/dm~3、0.30-1.19 mg/dm~3。茶树吸收根生物量和各养分含量随月份变化呈现双峰型,峰值分别在8月和翌年1月,而7月和11月生物量和养分储量均较低。与不施肥对照相比,施用氮肥影响茶树吸收根生物量,氮肥施用对茶树吸收根生物量的影响因氮肥施用时间而异。不同氮肥施用水平下茶树吸收根总碳浓度和总碳含量均不存在显著差异。受氮肥施用时间影响,施氮对茶树吸收根氮浓度的影响不同月份间存在差异,其中7月、8月和1月施氮处理下氮浓度较高,而9月、10月和11月不施氮处理下氮浓度较高。氮肥施用对各月份茶树吸收根氮养分储量均没有显著影响。氮肥施用降低了部分月份茶树吸收根磷、钾和镁的浓度和储量。施用中等用量的氮肥能缩小茶树吸收根夏秋季氮磷钾镁养分储量的月份间差异。     

不同镉水平下大麦幼苗生长和镉及养分吸收的品种间差异

利用水培试验研究了不同Cd水平下大麦幼苗的Cd和几种矿质元素吸收、积累、生长和生物学产量的品种间差异 .结果表明 ,1μmol·L-1Cd处理显著降低麦苗株高、绿叶数、叶绿素计读数、地上部和根系干重 ,显著抑制植株对Zn、Mn、Cu的吸收和累积 ;品种之间存在着显著差异 ,无芒六棱受抑制最为严重 ,米麦 114和浙农 1号表现出相对较强的抗性 .麦苗Cd含量和累积量品种之间也有显著差异 ,浙农 1号的Cd含量最高 ,米麦 114最低 .相关分析表明 ,麦苗生物学产量与地上部Cd含量、累积量及根系Cd含量呈显著负相关 ,其中与地上部Cd含量的相关性最强 ,与根系Cd累积量无显著相关 .     

不同浓度Al3+胁迫对水稻根生长的影响

铝毒害是酸性土壤限制农作物产量的主要因素之一。本文以水稻为材料,探讨了不同浓度的AlCl3(0、50、100、150 mmol.L-1)胁迫处理对水稻幼苗根生长的影响。结果表明,随着Al3+浓度和胁迫时间的增加,水稻幼苗根的生长受到抑制,长度和鲜重都减小,根尖细胞死亡的程度增大,根中H2O2含量上升;与对照(未经DMTU预处理)相比,经dimethylthiourea(内源过氧化氢抑制剂)预处理的水稻幼苗在Al3+胁迫下根细胞死亡程度减小,H2O2含量降低,根的生长抑制得到缓解,表明内源H2O2的积累是造成Al3+对水稻幼苗根生长抑制的原因之一。     

硝态氮(NO-3)对水稻侧根生长及其氮吸收的影响

侧根是植物吸收利用土壤养分的重要器官,其生长发育受内部遗传因子和外部环境矿质养分的影响.通过琼脂分层培养发现:局部供应NO-3可以诱导水稻( Oryza sativa L.)主根或不定根上侧根的生长.为研究旱种条件下NO-3对水稻侧根发育及其N吸收的影响,设置了3个蛭石培养实验:分根处理、全株缺N、全株供N处理.分根处理(一半根系供应3 mmol/L KNO3,另一半根系供应3 mmol/L KCl)结果表明:局部供应NO-3 能够促进水稻侧根生长.而在全株处理下,N饥饿诱导了侧根的伸长.水稻根系对NO-3的这两种反应都存在着显著的基因型差异.同时对地上部N浓度、可溶性总糖含量及N含量分析表明,这些生理指标在分根处理与全株加N处理中的差异均不显著,表明分根处理也能基本满足植株正常生长对N的需求.在分根处理中,水稻的N含量与分根处理中供N一侧的平均侧根长度存在显著正相关,这表明在养分不均一的介质中,侧根长度对水稻N素吸收具有十分重要的作用.而在N素充足的条件下,两者之间的相关性并不显著,这暗示在养分充足的环境下,侧根长度可能并不是决定根系吸收N素的主要因素.     

铵离子对不同基因型水稻吸收硝酸根离子的影响

NH4^ 可在很短时间内影响两种不同水稻亚种吸收NO36－,即可影响NO3^－的最初跨膜运输。籼型稻在NH4^＋存在时对NO3^－吸收促进,而粳型稻NO3^－吸收则明显减少。     

根表铁氧化物胶膜对水稻吸收Zn的影响

采用营养液培养方法研究了水稻根表形成的铁氧化物胶膜对水稻吸收Ｚｎ的影响．结果表明,在有Ｆｅ２＋的嫌气环境中,由于根际氧化作用水稻根表会形成红色的铁氧化物胶膜,根表的铁氧化物胶膜影响水稻对Ｚｎ的吸收．铁膜数量较少时,由于对Ｚｎ的富集作用有限,其对水稻Ｚｎ的吸收虽有促进作用,但不明显．随着根表铁膜数量的增加,这种促进作用也相应增加,并且在铁膜数量增加到一定值时,对水稻吸收Ｚｎ的促进作用达到最大．而后,随着铁膜数量的进一步增加,铁膜反而阻碍水稻对Ｚｎ的吸收,成为水稻吸收Ｚｎ的障碍层．在此过程中,水稻的根分泌物,特别是其中的植物铁载体对覆有铁膜水稻根系吸收Ｚｎ有促进作用．这种促进作用随铁膜数量的增加而逐渐减弱．因此,根表铁氧化物胶膜对水稻吸收Ｚｎ并不总是起促进作用,其作用的方向和程度取决于铁膜的数量．     

Comparative reactivity of triorganosilanes, HSi(OEt)3 and HSiEt3, with IrCl(CO)(PPh3)2. Formation of IrCl(H)2(CO)(PPh3)2 or Ir(H)2(SiEt3)(CO)(PPh3)2 depending on the substituents at Si

Reaction of HSi(OEt)₃ with IrCl(CO)(PPh₃)₂ (5:1 molar ratio) at room temperature for 1 h gives IrCl(H){Si(OEt)₃}(CO)(PPh₃)₂ (1), which is observed by the ¹H and ³¹P{¹H} NMR spectra of the reaction mixture. The same reaction, but in 20:1 molar ratio at 50 °C for 24 h produces IrCl(H)₂(CO)(PPh₃)₂ (2) rather than the expected product Ir(H)₂{Si(OEt)₃}(CO)(PPh₃)₂ (3) that was previously reported to be formed by this reaction. Accompanying formation of Si(OEt)₄, (EtO)₃SiOSi(OEt)₃, and (EtO)₂HSiOSi(OEt)₃ is observed. On the other hand, trialkylhydrosilane HSiEt₃ reacts with IrCl(CO)(PPh₃)₂ (10:1 molar ratio) at 80 °C for 84 h to give Ir(H)₂(SiEt₃)(CO)(PPh₃)₂ (4) in a high yield, accompanying with a release of ClSiEt₃.     

Sn-S and Ru-Ru bonds cleavage reactions between [Ph3SnS(CH2)3SSnPh3] and Ru3(CO)12: X-ray crystal structures of [Ph3SnS(CH2)3SSnPh3] and trans-[Ru(CO)4(SnPh3)2]

The organotin complex [Ph₃SnS(CH₂)₃SSnPh₃] (1) was synthesized by PdCl₂ catalyzed reaction between Ph₃SnCl and disodium-1,3-propanedithiolate which in turn was prepared from 1,2-propanedithiol and sodium in refluxing THF. Reaction of 1 with Ru₃(CO)₁₂ in refluxing THF affords the mononuclear complex trans-[Ru(CO)₄(SnPh₃)₂] (2) and the dinuclear complex [Ru₂(CO)₆(μ-κ²-SCH₂CH₂CH₂S)] (3) in 20 and 11% yields, respectively, formed by cleavage of Sn-S bond of the ligand and Ru-Ru bonds of the cluster. Treatment of pymSSnPPh₃ (pymS = pyrimidine-2-thiolate) with Ru₃(CO)₁₂ at 55-60 °C also gives 2 in 38% yield. Both 1 and 2 have been characterized by a combination of spectroscopic data and single crystal X-ray diffraction analysis.     

Solution-mediated syntheses and characterizations of two new zincophosphites [C6H14N2]0.5[Zn(H2PO3)2] and [C4H12N2]0.5[(CH3)2NH2][Zn2(HPO3)3]

Two new zincophosphites [C₆H₁₄N₂]_0.5[Zn(H₂PO₃)₂] 1 and [C₄H₁₂N₂]_0.5[(CH₃)₂NH₂][Zn₂(HPO₃)₃] 2 have been solvothermally synthesized in mixed solvents of N,N-dimethylformamide (DMF) and 1,4-dioxane (DOA), respectively. Single-crystal X-ray diffraction analysis reveals that compound 1 exhibits a neutral inorganic chain formed by ZnO₄ and HPO₂(OH) units. Interestingly, the left- and right-handed hydrogen-bonded helical chains are alternately formed via the hydrogen-bonds between two adjacent chains. Compound 2 exhibits a layer structure with 4- and 12-MRs formed by ZnO₄ and HPO₃ units, in which two kinds of organic amine molecules both act as countercations to compensate the overall negative electrostatic charge of the anionic network.     

Syntheses and characterization of the W(II) and W(III) N2 complexes, [WCl2(PMe3)3]2N2 and [WCl3(PMe3)2]2N2

Refluxing WCl₄(PMe₃)₃ under a nitrogen atmosphere in the presence of two equivalents of sodium amalgam leads to a reduction to the W(II) complex [cis,mer-WCl₂(PMe₃)₃]₂N₂ (1), which can be converted to [mer,trans-WCl₃(PMe₃)₂]₂N₂ (2) via appropriate oxidation/chlorination. Structural data have been obtained for both complexes, and demonstrate significantly increased steric crowding in 1 due to PMe₃/PMe₃ interactions. The N-N bond distances in the two compounds are similar, at 1.279(4) and 1.243(18) Å, respectively.     

Synthesis and characterisation of a trinuclear uranyl complex: Crystal structure of (CN3H6)5[(UO2)3O(OH)2(CH3COO)(C2O4)3]

The reaction of uranyl oxalate trihydrate with guanidinium acetate at room temperature in water yields known uranyl complex with composition (CN₃H₆)₂[UO₂(C₂O₄)₂(H₂O)]·H₂O as a first phase and a novel complex (CN₃H₆)₅[(UO₂)₃O(OH)₂(CH₃COO)(C₂O₄)₃] as a second. The second phase was investigated by means of IR spectroscopy and X-ray diffraction. The trinuclear discrete complex contains two symmetrically independent uranyl ions with a pentagonal bipyramid structure and has a nonplanar geometry. The distortion of its equatorial plane is caused by substitution of a monodentate bridge hydroxide anion by a bidentate bridge acetate-anion. The acidic ligands found in the complex are usually in competition for a place in coordination sphere of an uranyl ion, thus peculiarities of the complex formation are discussed in terms of ‘crystallochemical analysis’.     

Syntheses and structures of the heterometallic clusters [(Ph3PAu)3Re(CO)4], [(Ph3PAu)4Re(CO)4], [(Ph3PAu)6AuRe2(CO)8], and [(Ph3PAu)6Re(CO)3]

The reaction of [HRe₃(CO)₁₂]²⁻ with an excess of Ph₃PAuCl in CH₂Cl₂ yields [(Ph₃PAu)₄Re(CO)₄]⁺ as the main product, which crystallizes as [(Ph₃PAu)₄Re(CO)₄]PF₆ · CH₂Cl₂ (1 · CH₂Cl₂) after the addition of KPF₆.The crystal structure determination reveals a trigonal bipyramidal Au₄Re cluster with the Re atom in equatorial position.If [(Ph₃PAu)₄Re(CO)₄]⁺ is reacted with PPh₄Cl, a cation [Ph₃PAu]⁺ is eliminated as Ph₃PAuCl, and the neutral cluster [(Ph₃PAu)₃Re(CO)₄] (2) is formed.It combines with excess [(Ph₃PAu)₄Re(CO)₄]⁺ to afford the cluster cation, [(Ph₃PAu)₆AuRe₂(CO)₈]⁺. It crystallizes from CH₂Cl₂ as[(Ph₃PAu)₆AuRe₂(CO)₈]PF₆ · 4CH₂Cl₂ (3 · 4CH₂Cl₂). In [(Ph₃PAu)₃Re(CO)₄] the metal atoms are arranged in form of a lozenge while in [(Ph₃PAu)₆AuRe₂(CO)₈]⁺ two Au₄Re trigonal bipyramids are connected by a common axial Au atom.The treatment of [(Ph₃PAu)₄Re(CO)₄]⁺ with KOH and Ph₃PAuCl in methanol yields the cluster cation [(Ph₃PAu)₆Re(CO)₃]⁺, which crystallizes with from CH₂Cl₂ as [(Ph₃PAu)₆Re(CO)₃]PF₆ · CH₂Cl₂ (4 · CH₂Cl₂). The metal atoms in this cluster form a pentagonal bipyramid with the Re atom in the axial position.     

Oxoselenide triangular molybdenum clusters: Synthesis and characterization of [Mo3SeO3(acac)3(py)3]PF6

New cluster complex [Mo₃SeO₃(acac)₃(py)₃]⁺ was obtained by ligand substitution in the aqua complex [Mo₃SeO₃(H₂O)₉]⁴⁺. Crystal structure was determined for [Mo₃SeO₃(acac)₃(py)₃]PF₆·C₆H₅CH₃. The complex was characterized by ⁷⁷Se NMR, electrospray mass-spectrometry, and cyclic voltammetry. DFT calculations were used to confirm the assignment of chemical shift and to study Mo-Mo bonding in the cluster core.