石灰性土壤供氮能力几种化学测定方法的评价研究

以采自于黄土高原差异较大的25个农田耕层石灰性土壤为供试土样,以淋洗和未淋洗土壤起始NO3--N小麦和玉米两季盆栽试验作物累积吸氮量为参比,对8种反映旱地土壤供氮能力的化学方法进行比较研究。结果表明,在一定程度上,可用有密切关系的土壤全氮或有机质,反映有机氮或全氮存在较大差异的土壤供氮能力,但其灵敏性较差。石灰性土壤矿质氮,特别是NO3--N与未淋洗土壤起始NO3--N作物吸氮量之间有较高相关性(r=0.884,P<0.01),而与淋洗土壤起始NO3--N作物吸氮量间相关系数仅为0.472(P<0.05),说明矿质氮可反映土壤当前供氮水平,而不能反映土壤潜在供氮能力;石灰性土壤起始NO3--N对各化学方法与作物吸氮量之间相关性影响较大。酸性高锰酸钾法既可反映土壤潜在供氮能力,也可反映土壤总供氮能力;酸性高锰酸钾法的修订方法,即硫酸—高锰酸钾法提取出的NH4+-N值接近于KCl水浴法提取出的NH4+-N值,该方法在反映土壤总供氮能力方面与酸性高锰酸钾法相当,但在反映土壤潜在供氮能力方面不及酸性高锰酸钾法优越。KCl水浴法在评价石灰性土壤供氮能力方面,与酸性高锰酸钾法的效果基本相同;沸水浸取法和NaHCO3-UV...

水蚀条件下不同土壤氮素和有机质流失规律

人工模拟放水冲刷试验研究结果表明 ,随放水冲刷强度的增大 ,不同土壤硝态氮、铵态氮、有机质和全氮流失加剧 ,泥沙全氮和有机质富集程度减少 ;当给不同土壤施等量的硝酸铵时 ,发现随径流流失化肥的铵态氮和硝态氮分别占施入量的 0 .9%～ 3 .5 %和 8.2 %～ 19.7% ,硝酸铵主要随径流流失 ,以泥沙颗粒流失量甚微 ;土壤侵蚀、有机质和全氮流失量与 >2 0 μm团聚体相关系数分别为 -0 .893 5、-0 .792 8和 -0 .815 1,2 0 μm直径的团聚体是区分土壤有机质和全氮流失的标准

黄土区退果还耕对黑垆土硝态氮积累和迁移的影响

在黄土高原沟壑区王东沟小流域,针对塬面、梁地和坡地三种地形,分别选取了盛果期果园、老果园和退果还耕地等,研究了退果还耕条件下,三种地貌类型土壤剖面中水分含量变化及NO_3~--N、NH_4~+-N积累和迁移规律。结果表明,无论塬面、梁地或者坡地上,果园土壤水分含量显著降低(10%～14%);果园退耕后,土壤水分开始缓慢恢复。盛果期,塬面NO_3~--N峰值主要处于100—200 cm之间,退果还耕后,100 cm以上土层中NO_3~--N含量降低,100cm以下NO_3~--N积累量在增加,并且峰值不断向下移动。盛果期果园NO_3~--N积累量为631～3032 kg/hm~2;退果还耕地、老果园NO_3~--N积累量都显著高于盛果期果园。盛果期40%以上的NO_3~--N积累在100—200 cm土层,但退果还耕地上50%左右集中分布在200—300 cm土层。土地利用与管理方式的变化对NH_4~+-N分布特征的影响并不明显。

玉米地膜覆盖的土壤环境效应

通过田间试验研究了地膜覆盖和露地栽培对玉米的土壤温度、水分、养分、盐分含量和土壤生物学特性及硝酸盐含量的变化。结果表明,在玉米生长前期,地膜覆盖5,10,15,20,25 cm土层的土壤日平均温度比露地提高2.4℃、3.0℃、2.9℃、2.2℃、2.7℃,6~7月份比露地降低1.1℃、0.5℃、0.5℃、0.6℃、0.6℃。地膜覆盖0~10,10~20,20~30,30~40 cm土层的土壤含水量分别比露地增加18.84%、10.67%、11.12%和8.9%。地膜覆盖增强了土壤蔗糖酶和碱性磷酸酶的活性,增加了土壤微生物的数量、CO2浓度、土壤呼吸和土壤NO3--N的含量,减少了土壤氮素的损失。地膜覆盖降低了土壤有机质、氮素、速效磷的含量、过氧化氢酶和脲酶的活性及土壤表层的盐分含量。地膜覆盖提高了玉米的生物量和经济产量。

不同施氮水平和杂草清除时间对半湿润地区农田氮素利用及产量的影响

在半湿润地区中等肥力土垫旱耕人为土上进行田间试验,通过对冬小麦不同生育期杂草和作物样品的采集与分析,研究不同施肥及杂草处理对氮肥肥效的影响。结果表明:作物吸氮量随施氮量增加而增加,杂草吸氮量随吸氮量增加而降低;在不同杂草处理全生育期不清除杂草(A)、越冬前清除杂草(B)、返青期清除杂草(C)和拔节期清除杂草(D)的各个处理中,A、B、C和D杂草吸氮量分别占农田植物(作物+杂草)地上部分总吸氮量的1.98%、1.39%、3.99%和3.82%。籽粒产量随施氮量增加而增加,施氮量为135 kg N.hm-2时产量最高,达5 645.1 kg.hm-2,施氮量高于135 kg N.hm-2时,产量趋于稳定。氮肥利用率、氮肥利用效率、氮肥农学效率和氮肥生理效率均随施氮量增加而降低;从不同杂草处理看,以全生育期不清除杂草处理氮肥利用率最高,达到43.8%,返青期清除杂草处理氮肥利用率最低,为26.3%,二者间差异达显著水平;氮肥利用效率以越冬期清除杂草处理最高,为42.8 kg.kg-1N,全生育期不清除杂草处理最低,为40.6kg.kg-1N;氮肥生理效率以返青期清除杂草处理最高,为57.5 kg.kg-1N,显著高...

氮素形态和铁营养对玉米苗期生长及体内铁分布的影响

以玉米(Zea mays)品种‘豫玉-22’为材料,采用营养液培养方法,研究了低铁和正常供铁条件下供应不同形态氮素对玉米苗期生长及体内铁分布的影响。结果表明:(1)与低铁介质相比,常铁介质增加了各氮素处理玉米幼苗的株高、地上部干重、全株干重,降低了根冠比,其中硝态氮处理表现得尤其突出;与供应硝态氮(NO3--N)相比,增施铵态氮(1/2 NO3--N+1/2 NH4+-N,NH4+-N)能明显促进低铁介质中玉米生长,但在常铁介质下作用不明显。(2)相比于低铁介质,正常供铁显著提高了相应处理玉米新叶叶绿素含量及净光合速率;2种供铁介质中,NH4+-N处理的新叶叶绿素含量以及净光合速率均高于其它氮素处理。(3)相比于低铁介质,正常供铁处理总体上增加了玉米各部分活性铁含量和全铁含量,对NO3--N处理的新叶活性铁含量增加尤其明显;2种供铁介质中,NH4+-N均有利于提高新叶活性铁含量和植株地上部全铁含量。(4)玉米新叶活性铁含量不仅与其叶绿素含量显著正相关(r=0.979**),也与叶片净光合速率显著正相关(r=0.950**)。研究发现,供铁状况显著影响玉米新叶的叶绿素含量及其净光合速率且与供氮形态存在互作;供应...

设施条件下氮肥对大青菜硝酸盐及土壤矿质氮累积的影响

采用田间实验研究了施用氮肥对设施条件下大青菜生长发育和产量,以及对土壤硝酸盐含量累积分布的影响。结果表明,在施氮肥0~500 kg hm-2范围内,氮肥施用量越大,产量越高,但到达一定量时,便不能再促进产量的提高,反而会引起减产。土壤铵态氮含量随着土壤剖面向下不断下降,表层的铵态氮含量较高,土壤硝态氮含量在整个土壤剖面的分布变化较小,但也是从表层向下处于一种缓慢减少的趋势,铵态氮的累积主要集中在上部土壤剖面,硝态氮的累积分布在整个土壤剖面,土壤硝态氮含量随施肥量增加而增加;氮肥施用量对硝酸盐含量有很大影响。在施氮肥0~700kg hm-2范围内,氮肥施用量越多,大青菜硝酸盐含量越高。

蔬菜温室土壤某些化学性质的演变特征

To explore the changes of soil chemical properties in vegetable greenhouse,a comparative study was carried out with the samples gathered from vegetable greenhouse fields and their adjacent upland fields in Damintun Town,Xinming County,Liaoning Province.The results showed that compared with upland fields,the contents of soil organic carbon and total nitrogen in greenhouse fields increased significantly.At the depth of 0～30 cm,soil organic carbon in greenhouses of 1-,4-and 10-year increased by 31.09%,35.44%,and 66.80%,respectively,compared with the upland soil.Soil nitrate content at the depth of 0～30 cm in greenhouse fields was 5.05～12.49 times as much as that in upland fields.The nitrate content in different soil layers increased with the increasing age of greenhouse field.,e.g.,at the depth of 20～30 cm,soil nitrate content was significantly higher in 10-year than in 1-and 4-year greenhouse field,with an increase of 65.73% and 50.89%,respectively,and 6.55 times as much as that in upland field,which indicated that soil nitrate transported downwards,and obviously enriched in deeper soil layers under heavy application of fertilizer.Also with the increasing age of greenhouse field,soil pH decreased,while soil soluble salts accumulated.

一种拟南芥突变体对高浓度CO_2反应的研究

The study on the response of a mutant and a wild type of Arabidopsis to 660 μl·L -1 CO 2 and ambient CO 2 showed that under elevated CO 2,the stomatal numbers of the mutant increased,while those of the wild type decreased. The chlorophyll content and NR (nitrate reductase) activity of the mutant increased,but those of the wild type had no obvious response. The mutant was not reproductively mature after the continuous exposure to increased CO 2 for five months. The results provided evidence of plant response to the changes of atmospheric CO 2 concentration,and the clues to related studies on other plants.

Hollow fibers of yttria-stabilized zirconia (8YSZ) prepared by calcination of electrospun composite fibers

8YSZ fibers were synthesized by calcination of PVP/zirconium oxychloride/yttrium nitrate composite fibers (PVP-Precursor) obtained by electrospinning. Scanning electron microscopy (SEM) indicated that the 8YSZ fibers are hollow and the gas released during organic binder decomposition resulted in the formation of hollow center in fibers

One-pot synthesis of silver nanoplates and charge-transfer complex nanofibers

We describe a facile one-pot process to synthesize Ag nanoplates by reducing silver nitrate with 3,3',5,5'-tetramethylbenzidine (TMB) at room temperature. The silver nanoplates were highly oriented single crystals with (111) planes as the basal planes. TMB can be readily oxidized to charge-transfer (CT) complex between TMB, as a donor, and (TMB)(2+), as an acceptor. The pi-pi interaction of the neutral amine (TMB) and diiminium structure (dication, TMB2+) result in the formation of one-dimensional CT complex nanofiber.

Sonochemical synthesis of monodispersed KY3F10 : Eu3+ nanospheres with bimodal size distribution

Monodispersed KY3F10:Eu3+ nanospheres with bimodal size distribution have been successfully synthesized via a facile and efficient sonochemical method in a surfactant-free system. Rare-earth nitrate (Y, Eu)(NO3)(3) and potassium fluoborate (KBF4) were used as precursors. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and photoluminescence (PL) spectra were used to characterize the samples.

The separation of Cerium(IV) from nitric acid solutions containing Thorium(IV) and Lanthanides(III) using pure [C(8)mim]PF6 as extracting phase

The extraction behavior of Ce(IV) along with Th(IV) and Ln(III) (Ln = Ce, Gd, Yb) nitrate by pure ionic liquid, [C(8)mim]PF6, was investigated. [C(8)mim]PF6 alone showed good extraction ability for Ce(IV), while it was slight for Th(IV) and negligible for Ln(III). The extraction behavior of Ce(IV) by [C(8)mim]PF6 was particularly studied, and the most probable extraction mechanism proposed was the anion exchange mechanism. Moreover, the stripping of Ce(IV) from IL phase was also investigated. The Ce(IV) in IL phase can be quantitatively recovered by water.

Extraction kinetics of thorium(IV) with primary amine N1923 in sulfate media using a constant interfacial cell with laminar flow

Extraction kinetics of thorium(IV) with primary amine N1923 in sulfate media has been investigated by a constant interfacial cell with laminar flow. Studies of interfacial tension and effects of the stirring rate, temperature, and specific interfacial area on mass transfer rate show that the most probable reaction zone takes place at the liquid-liquid interface. According to the experimental data correlated as a function of the concentration of the relevant species involved in the extraction reaction, the rate equation of extracting thorium has been obtained as follows: -d[Th(IV)]((o))/dt = 10(-3.10)center dot[Th(IV)](0.89)center dot[(RNH3)(2)SO4](0.74).

Poly[[diaqua-mu-4,4 '-bipyridine-dinitratodi-mu-L-tyrosinato-dicopper(II)]: a chiral two-dimensional coordination polymer

The title compound, [Cu-2(C9H10NO3)(2)(NO3)(2)(C10H8N2)-(H2O)(2)](n), contains Cu-II atoms and L-tyrosinate (L-tyr) and 4,4'-bipyridine (4,4'-bipy) ligands in a 2:2:1 ratio. Each Cu atom is coordinated by one amino N atom and two carboxylate O atoms from two L-tyr ligands, one N atom from a 4,4'-bipy ligand, a monodentate nitrate ion and a water molecule in an elongated octahedral geometry. Adjacent Cu atoms are bridged by the bidentate carboxylate groups into a chain. These chains are further linked by the bridging 4,4'-bipy ligands, forming an undulated chiral two-dimensional sheet. O-H center dot center dot center dot O and N-H center dot center dot center dot O hydrogen bonds connect the sheets in the [100] direction. This study offers useful information for the engineering of chiral coordination polymers with amino acids and 4,4'-bipy ligands by considering the ratios of the metal ion and organic components.