下辽河平原降雨中氮素的动态变化

为了了解降雨中氮对农田生态系统的影响,分析了2004—2006年下辽河平原连续3年定位收集的降雨观测资料与历史资料。结果表明:降雨中氮输入量季节变化显著,夏季最高,这主要与降雨量及空气中NH4+-N浓度变化有关;降雨中DON量与NO3--N含量相当,均接近24%,是雨水中氮的重要组分;与1985年相比,近3年降雨输入到该地区农田生态系统的年氮通量已有较大提高,降雨较多的2005年输入的无机氮量更是20年前的2倍以上;2004—2006年随降雨输入农田生态系统的氮平均占可利用肥料氮的28.3%,对农田生态系统有着重要影响。

新型吡唑类化合物DL-1的硝化抑制效应初探

以国内外应用较为广泛的硝化抑制剂双氰胺(DCD)为参比对象,采用室内培养方法,对新型吡唑类化合物DL-1的硝化抑制效应进行初步探讨.结果表明,DL-1对土壤中铵的氧化过程具有显著的抑制效应,前3周的硝化抑制率可达70%以上,且硝化抑制能力在第14天至28天最强.与等量DCD相比,施用量为(NH4)2SO4氮量1.0%的DL-1在14、21和28d使土壤中的NO3--N含量分别下降26.23%、33.27%和23.31%;与不加抑制剂的对照处理相比,土壤NO3--N含量则分别下降了71.12%、69.10%和55.14%.当DL-1用量为(NH4)2SO4氮量的2.0%时,土壤的硝化作用受到了更强烈的抑制,到培养第90天试验结束,土壤中的NO3--N含量始终维持在较低水平.

新型脲酶抑制剂LNS与双氰胺配合施用对菜田土壤尿素氮转化及蔬菜生长的影响

采用微区试验方法,初步探讨了新型脲酶抑制剂LNS及其与硝化抑制剂双氰胺(DCD)配合施用对菜田土壤尿素氮转化和蔬菜生长的影响。结果表明,LNS对土壤脲酶活性可以起到一定的抑制作用,从而延迟尿素N在土壤中的水解和NH4+-N的释放高峰期,其发挥作用的时间大约在施用后前10天。LNS与DCD配合施用则能显著抑制尿素水解后NH4+的氧化作用,使蔬菜整个生长期内的NO3--N含量维持在较低水平。抑制剂的施用对芹菜产量虽然没有产生显著影响,但可以降低其体内硝酸盐含量,并提高芹菜干物质含量。

畜禽粪便堆肥过程中各种氮化合物的动态变化及腐熟度评价指标

对不同畜禽粪便在堆肥过程中各种含氮化合物的动态变化进行了研究,结合综合性腐熟度评价指标——种子发芽指数(GI),探讨了畜禽粪便堆肥过程中与氮有关的腐熟度评价指标.结果表明:随着堆肥的进行,除奶牛粪外,其它畜禽粪便的全氮(TN)含量均呈先下降而后平稳变化趋势,奶牛粪则呈先增加而后平稳变化趋势;各种畜禽粪便中,碱解性氮(HN)含量先增后降;NH4+-N含量先下降而后保持平稳;NO3--N含量则持续增加;NH4+-N/NO3--N迅速降低.堆肥腐熟度指标中,除综合性评价指标GI值外,HN/TN和NH4+-N/TN也可作为评价畜禽粪便腐熟程度的优选指标,而NO3--N/TN只能作为一般性评价指标.根据综合性评价指标GI值达到腐熟要求的标准(GI>0.50),除仔猪粪外,其它畜禽粪便在HN/TN<20.77%、NH4+-N/TN<10.06%及NO3--N/TN>0.38%时基本达到腐熟要求.

乙炔抑制型基质氮肥养分释放模式初探

将(NH4)2SO4中加入占其纯N质量2%的乙炔前体——电石,用一种疏水性材料将其胶结造粒,制成基质型缓释氮肥,通过土壤溶出实验与作物栽培实验表征其养分释放模式。结果表明,其养分释放模式为扩散控制型,释放模式可看作包膜肥料的非线性组合,疏水材料的物理阻滞力与乙炔(C2H2)的硝化抑制作用能形成较好的"缓释接力"效应,且C2H2的硝化抑制率要优于同条件下的双氰胺(DCD),同时期乙炔处理的作物生物量也高于DCD处理。

抑制剂对尿素转化及土壤中氮的影响研究

以草甸棕壤为基质进行室内培养试验结果表明,脲酶抑制剂与硝化抑制剂配合使用,明显地抑制了NH4+-N向NO3--N的转化。NBPT+DCD处理效果最好,可延缓硝态氮的释放高峰达40天以上;H1和HA都表现出较强的硝化抑制作用。H3和H2对硝态氮基本无影响。

影响土壤N_2O排放和CH_4吸收的主控因素的研究(英文)

本文于2000年7月,在实验室模拟条件下,以长白山阔叶红松林鲜土壤为对象,采用正交试验设计法对土壤进行培养实验,研究了影响土壤N2O排放和CH4吸收的主要因素。考察了温度、水分、pH值、NH4+及NO3-五因素对森林土壤N2O排放和CH4吸收的影响。实验结果显示:在本试验设计的因素、水平条件下,N2O排放速率、CH4吸收速率二者均与土壤pH值和温度这两个因素呈显著正相关。并且N2O排放速率与CH4吸收速率间呈显著线性正相关关。

与氮转化有关的土壤酶活性对抑制剂施用的响应

利用室内模拟培养试验 ,研究好气条件下施用尿素后土壤脲酶、硝酸还原酶、亚硝酸还原酶和羟胺还原酶活性对脲酶抑制剂氢醌 (HQ)与硝化抑制剂包被碳化钙 (ECC)和双氰胺 (DCD)组合 (HQ +ECC、HQ +DCD)的响应 .结果表明 ,HQ +DCD组合与其它抑制剂处理相比能更有效地降低土壤脲酶活性 ,增加硝酸还原酶、亚硝酸还原酶、羟胺还原酶活性 .不同处理土壤脲酶、亚硝酸还原酶和羟胺还原酶活性与土壤NH4 + 、NO3-、NH3 挥发和N2 O排放速率间存在不同形式的显著相关关系 .土壤脲酶、亚硝酸还原酶和羟胺还原酶活性之间亦存在不同形式的显著正相关关系 .

玉米苗期施用缓/控释氮素肥料养分释放特点与土壤生物活性研究

采用盆栽试验,模拟田间生态环境,测定施用不同种缓/控释氮素肥料,玉米苗期土壤尿素态氮、硝态氮、铵态氮含量,脲酶、硝酸还原酶活性、微生物量碳和氮含量变化趋势,比较玉米苗期氮素养分释放、土壤生物活性特点。研究表明,玉米苗期,施用SA+nBPT+U肥料,尿素态氮和NH4+-N的积累量最多,对土壤脲酶活性有显著的抑制作用;SA+U肥料,硝态氮最多;MMA+nBPT+U肥料,尿素自膜内迁移到土壤中的量较少,硝态氮和微生物量最少。包膜与脲酶抑制剂nBPT相结合的缓/控释肥料,对减少硝态氮的生成效果最为明显。施用nBPT+U肥料,微生物量最多。施用不同种缓/控释氮素肥料,土壤硝酸还原酶活性普遍增强,脲酶抑制剂nBPT对土壤硝酸还原酶活性无显著作用;施用不同种缓/控释氮素肥料土壤微生物量碳、氮的变化趋势一致。丙烯酸树脂包膜与脲酶抑制剂相结合的缓/控释肥料控释效果最好。

Two novel molybdenum complexes containing [Mo2O2S2](2+) fragment: synthesis, crystal structures and catalytic studies

Mo2O2S2(HGly)(GlY)(2) 1 and K-6[Mo2O2S2(nta)(2)][Mo2O2S2(ntaH)(2)]center dot 4H(2)O 2 were synthesized by the reactions of (NH4)(2)MoS4 and amino acids L (L = glycine, nitrilotriacetic acid) in ethanol-water medium at ambient temperature. The two complexes were characterized by elemental analysis, infrared spectra, UV-visible spectra, TG-DTA and XPS.

Studies of the intermolecular DNA triplexes of C+center dot GC and T center dot AT triplets by electrospray ionization Fourier-transform ion cyclotron resonance mass spectrometry

Formation and stabilities of four 14-mer intermolecular DNA triplexes, consisting of third strands with repeating sequence CTCT, CCTT, CTT, or TTT, were studied by electrospray ionization Fourier-transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS) in the gas phase. The gas-phase stabilities of the triplexes were compared with their CD spectra and melting behaviors in solution, and parallel correlation between two phases were obtained. In the presence of 20 mm NH4+ (pH 5.5), the formation of the TTT triplex was not detected in both solution and the gas phase.

High activity PtRu/C catalysts synthesized by a modified impregnation method for methanol electro-oxidation

A modified impregnation method was used to prepare highly dispersive carbon-supported PtRu catalyst (PtRu/C). Two modifications to the conventional impregnation method were performed: one was to precipitate the precursors ((NH4)(2)PtCl6 and Ru(OH)(3)) on the carbon support before metal reduction: the other was to add a buffer into the synthetic solution to stabilize the pH. The prepared catalyst showed a much higher activity for methanol electro-oxidation than a catalyst prepared by the conventional impregnation method. even higher than that of current commercially available, state-of-the-art catalysts. The morphology of the prepared catalyst was characterized using TEM and XRD measurements to determine particle sizes, alloying degree, and lattice parameters. Electrochemical methods were also used to ascertain the electrochemical active surface area and the specific activity of the catalyst.

catena-Poly[diammonium [diaquabis(pyridine-2,4-dicarboxylato-kappa N-2,O-2)cuprate(II)] [[diaquacopper(II)]-mu-pyridine-2,4-dicarboxylato-kappa N-3,O-2:O-2 '-[tetraaquacadmium(II)]-mu-pyridine-2,4-dicarboxylato-kappa O-3(2):N,O-2 '] hexahydrate]

The title mixed-metal complex, {(NH4)(2)[Cu(C7H3NO4)(2)(H2O)(2)][CdCu(C7H3NO4)(2)(H2O)(6)]center dot 6H(2)O}(n), contains one octahedrally coordinated Cd-II center and two octahedrally coordinated Cu-II centers, each lying on an inversion center. The two Cu-II atoms are each coordinated by two O atoms and two N atoms from two 2,4-pydc (2,4-H(2)pydc = pyridine-2,4-dicarboxylic acid) ligands in the equatorial plane and two water molecules at the axial sites, thus producing two crystallographically independent [Cu(2,4-pydc)(2)(H2O)(2)](2-) metalloligands. One metalloligand exists as a discrete anion and the other connects the Cd(H2O)(4) units, forming a neutral chain.

Bimolecular quadruplexes and their transitions to higher-order molecular structures detected by ESI-FTICR-MS

Four individual quadruplexes, which are self-assembled in ammonium acetate solution from telomeric sequences of closely related DNA strands - d(G(4)T(4)G(4)), d(G(3)T(4)G(4)), d(G(3)T(4)G(3)), and d(G(4)T(4)G(3)) - have been detected in the gas phase using electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS). The bimolecular quadruplexes associate with the same number of NH4+ in the gas phase as NMR shows that they do in solution. The quadruplex structures formed in solution are maintained in the gas phase. Furthermore, the mass spectra show that the bimolecular quadruplexes generated by the strands d(G(3)T(4)G(3)) and d(G(4)T(4)G(3)) are unstable, being converted into trimolecular and tetramolecular structures with increasing concentrations of NH4+ in the solution. Circular dichroism (CD) spectra reveal structural changes during the process of strand stoichiometric transitions, in which the relative orientation of strands in the quadruplexes changes from an antiparallel to a parallel arrangement. Such changes were observed for the strand d(G(4)T(4)G(3)), but not for the strand d(G(3)T(4)G(3)). The present work provides a significant insight into the formation of various DNA quadruplexes, especially the higher-order species.

Synthesis and structural characterization of new tungsten(VI) complexes with polycarboxylate ligands

The reactions of (NH4)(2)WS4 and three polycarboxylate ligands {including nitrilotriacetate (nta(3-)), citrate (Hcit(3-)) and ethylenediaminetetra acetate (EDTA(4-))} in H2O/EtOH at ambient temperature have resulted in three new trioxotungsten (VI) complexes, K-3[WO3(nta)]center dot H2O 1, (NH4)(4)[WO3(cit)]center dot 2 H2O 2 and K-2(NH4)(2)[W2O6(EDTA)]center dot 4H(2)O 3, respectively. These three complexes have been characterized by IR, XPS, TGA-DTA, H-1 and C-13 NMR spectroscopy. And their structures have been determined by X-ray crystallographic studies, which confirm that I and 2 are mononuclear compounds and 3 is a binuclear compound. Each tungsten atom in 1-3 is coordinated to three unshared oxygen atoms, which adopt fac stereochemistry, while the remaining fac positions are occupied by three atoms from the ligands. The electrochemical properties of 2 and 3 have been investigated.