两种种植密度下施肥对冬小麦生物学性状及产量的影响

以土垫旱耕人为土为供试土壤,采用大田试验,研究半湿润农田生态系统两种种植密度下不同施肥处理对冬小麦生物学性状及子粒产量的影响。试验设两种种植密度:常规密度(播种量为150.0kg/hm~2)和低密度(播种量为90.0kg/hm~2)。常规密度设7个施肥处理,即不施肥(CK),单施磷肥(PN0),单施氮肥(P0N135)和在施P的基础上每公顷施N45、90、135和180kg(即PN45、PN90、PN135、PN180);低密度施肥处理设不施肥(CK)、单施磷(PN0)、单施氮(P0N135)和氮磷配施(PN135)。结果表明,低密度时,CK处理分蘖数最低(每株平均3.2个),PN135分蘖数最高(每株平均6.9个);常规密度时,仍以CK分蘖数最低(每株平均3.2个),PN180分蘖数最大(每株平均6.8个)。低密度下,PN0和CK与P0N135和PN135间植株绿叶面积差异达显著水平(P<0.05),以PN135绿叶面积最大,PN0绿叶面积最小;常规密度下,PN180绿叶面积最大,为80.7cm~2/单茎,PN0绿叶面积最小,为44.4cm~2/单茎。低密度时,CK旗叶面积最小,PN135旗叶面积最大;常规...

辽东山区长白落叶松(Larixolgensis)种子雨和种子库

长白落叶松是东北地区主要的用材树种,其种子雨和种子库研究鲜见报道。在辽东山区用收集器收集的种子分析了长白落叶松种子雨组成、质量和扩散距离,每隔2个月调查1次种子库数量,并结合靛蓝染色法测定每次种子的活力来分析土壤种子库动态。结果表明,辽东山区的长白落叶松种子雨从8月中旬开始,9月末到10月初达到高峰期,11月初结束。在起始期,种子雨以干瘪的不完整种子为主,而从高峰期开始,种子雨以完整种子为主。整个长白落叶松种子雨中不完整种子约占种子雨总量的45%,这些不完整种子由被动物取食、空粒和病虫害危害种子组成。完整种子的平均生活力为56.4%,即有活力的种子仅占整个种子雨的30%。种子雨集中在母树周围,在林缘1次扩散距离一般不超过1.5倍树高。种子雨到达地面之后,主要分布在枯枝落叶层,土壤0~5cm层有少量分布,土壤5 cm以下没有种子分布;土壤种子库的种子主要在翌年雪融化后开始萌发、被取食、搬运以及腐烂,其中腐烂种子数占45.4%,动物取食为30.0%。种子库的种子数量和活力在冬季没有明显变化,而在翌年,种子数量和活力明显减少,4、6月和8月份种子数量分别为(506.3±35.56)粒m-2,(267.1±17.47)粒m-2和(143.6±9.83)粒m-2,对应的活力分别为47.8%±4.68%,19.4%±3.39%和0%,这表明长白落叶松种子不能在地面形成连续的种子库。

黄土丘陵区退耕地土壤水分入渗特征及影响因素

为评价退耕还林(草)工程的成效及认识下垫面改变对土壤水文过程的影响,采用圆盘入渗仪以4、6、8年退耕地为对象,长芒草草地为对照在黄土丘陵区分层(表层、20 cm、40 cm)研究退耕地土壤水分入渗特征,并探讨其影响因素。结果表明:1)较短年限退耕地表层土壤入渗能力较天然草地差,而下层入渗能力较天然草地强;2)退耕地下层的初始入渗速率是表层的1.2~1.4倍,稳定入渗率是表层的1.9~2.8倍,饱和导水率是表层的1.9~3.0倍;3)随着退耕年限增加,表层土壤入渗能力下降,而下层入渗能力增强;4)土壤结皮阻碍退耕地表层土壤的入渗。

施用泥炭对风沙土改良及蔬菜生长的影响

通过盆栽试验比较了施用不同剂量的泥炭 (0 %、2 %、5 %、8%及 10 % )对风沙土改良的效果和对白菜生长及产量的影响。结果表明 ,泥炭能增强风沙土的持水能力 ,降低土壤的pH值 ,增加土壤中有机质、全氮、速效氮和速效磷等的含量 ;白菜根系长度、生物量、高生长和地上部分的生物量均有增加 ,其中 8%泥炭处理为最佳 ,其根系长度、根鲜重、干重、高生长、地上部分鲜重、干重依次比对照增加 71%、4 0 2 %、4 6 4 %、10 7%、84 7%和 10 0 1% ;同时施用泥炭还有利于提高白菜干物质的积累及其品质

水、土壤及植物样品中1,2,4-三氯苯的提取和GC测定

<正> 1 引言三氯苯(1,2,4-TCB)是化学工业和合成农药的重要原料,但同时也是环境中广泛存在的污染物。早在1979年,1,2,4-TCB就被美国环保局列入129种优先控制的污染物之一。在我国1,2,4-TCB也是常见的一种有机污染物。水体和土壤中1,2,4-TCB的分析方法国内已见报道。但这些方法大多步骤复杂、操作困难,而且费时、试剂消耗量大。另外,目前尚没有植物样品中1,2,4-TCB分析方法的报道。本文建立了步骤简单、易操作、节约试剂的水、土壤、植物和作物籽实中1,2,4-TCB的提取和分析方法。

太阳辐射对长白山阔叶红松林净生态系统碳交换的影响

太阳辐射是植物进行光合作用的前提条件,因此成为影响植被吸收大气CO2的重要环境因子。该研究基于30min通量和常规气象数据,以相对辐射和晴空指数为指标,分析了2003～2006年生长旺季(6～8月)太阳辐射的改变对长白山阔叶红松(Pinuskoraiensis)林净生态系统碳交换(Netecosystemexchange,NEE)的影响。结果表明:天空有一定云层的覆盖对阔叶红松林碳的净吸收有明显的促进作用。4年里6～8月间生态系统最大光合速率在天空有云覆盖时较晴空条件下分别提高了34%、25%、4%和11

A Facile One-pot Synthesis of Substituted Pyridine-2,4(1H,3H)-diones from α-Acyl-α-carbamoyl Ketene-S,S-acetals

A facile and efficient one-pot synthesis of substituted pyridine-2,4(1H,3H)-diones has been developed. Subjected to N,N-dimethylformamide dimethyl acetal (DMFDMA) in N,N-dimethylformamide at 120 ˚C, a series of acyl(carbamoyl)ketene S,S-acetals were converted into the corresponding substituted pyridine-2,4(1H,3H)-diones in high yields.

Effect of the nucleating agent 1,3 : 2,4-di(3,4-dimethylbenzylidene) sorbitol on the gamma phase content of propylene/ethylene copolymer

The influence of the concentration of a nucleating agent (NA), namely 1,3:2,4-di(3,4-dimethylbenzylidene) sorbitol (DMDBS), on the gamma phase content in a propylene/ethylene copolymer was investigated by means of Differential Scanning Calorimetry (DSC), Wide-Angle X-ray Diffraction (WAXD), Small- Angle X-ray Scatter (SAXS) and Polarized Optical Microscopy (POM).

Thiophene-NPN Ligand Supported Rare-Earth Metal Bis(alkyl) Complexes. Synthesis and Catalysis toward Highly trans-1,4 Selective Polymerization of Butadiene

A series of new rare-earth metal bis(alkyl) complexes [L(1-3)Ln(CH2SiMe3)(2)(THF)(n)] (L-1 = MeC4H2SCH2NC6H4(Ph)(2)P=NC6H2Me3-2,4,6: Ln = Sc, n = 1 (1a); Ln = Lu, n = 1 (1b); L-2 = MeC4H2SCH2NC6H4(Ph)(2)P=NC6H3Et2-2,6: Ln = Sc, n = 1 (2a); Ln = Lu, n = 1 (2b); Ln = Y, n = 1 (2c); L-3 = MeC4H2SCH2NC6H4(Ph)(2)P=(NC6H3Pr2)-Pr-i-2,6: Ln = Sc, n = 0 (3a)) and (LSc)-Sc-4(CH2SiMe3)(2()THF) (4a) (L-4 = C6H5CH2NC6H4(Ph)(2)P=NC6H3Et2-2,6) have been prepared by reaction of rare-earth metal tris(alkyl)s with the corresponding HL1-4 ligands via alkane elimination.

Highly 3,4-selective living polymerization of isoprene with rare earth metal fluorenyl N-heterocyclic carbene precursors

Fluorenyl modified N-heterocyclic carbene ligated rare earth metal bis(alkyl) complexes, (Flu-NHC)Ln(CH2SiMe3)2 (Flu-NHC = (C13H8CH2CH2(NCHCCHN)C6H2Me3-2,4,6); Ln = Sc (1a); Ln = Y (1b); Ln = Ho (1c); Ln = Lit (1d)), were synthesized and fully characterized by NMR and X-ray diffraction analyses. Complexes Ib-d with the activation of (AlBu3)-Bu-i and [Ph3C][B(C6F5)4] exhibited high activity, medium syndio-but remarkably high 3,4-regio-selectivity, and the unprecedented livingness for the polymerization of isoprene. Such distinguished catalytic performances could be maintained under various monomer-to-initiator ratios (500-5000) and broad polymerization temperatures (25-80 degrees C).

New rare earth metal bis(alkyl)s bearing an iminophosphonamido ligand. Synthesis and catalysis toward highly 3,4-selective polymerization of isoprene

Newrareearth metal bis(alkyl) complexes [(NPNPh)Ln(CH2SiMe3)(2)(THF) (NPNPh:N(Ph)PPh2=NC6H2Me3-2,4,6; Ln = Sc (3a), Ln = Y (3b), Ln = Lu (3c)) and [(NPNPy)Sc(CH2SiMe3)(2)(THF)1 (NPNPY = N(Py)PPh2=NC6H2Me3-2,4,6) (3d)) have been prepared via protonolysis reaction between rare earth metal tris(alkyl)s and the corresponding iminophosphonamines. Complexes 3a-d are analogous monomers of THF solvate. Each metal ion coordinates to a eta(2)-chelated NPN ligand and two cis-located alkyl groups, adopting tetrahedron geometry.

Ethylene polymerization by (alpha-diimine)nickel(II) complexes bearing different substituents on para-position of imines activated with MMAO

A series of (alpha-diimine)nickel(II) complexes [ArN = C(Nap)C = NAr]NiBr2 (Nap = 1,8-naphthdiyl, Ar = 2,6-Me2C6H3, 3a; Ar = 2,4,6-Me3C6H2 3b; Ar = 2,6-Me-2-4-tBuC(6)H(2), 3c; Ar 2,6-Me-2-4-BrC6H2, 3d; Ar = 2,6-Me-2-4-ClC6H2, 3e; Ar 2,6-iPr(2)C(6)H(3), 3f; Ar = 2,4,6-iPr(3)C(6)H(2), 3g; Ar = 2,6-iPr-4-BrC6H2, 3h) have been synthesized, characterized, and investigated as precatalysts for ethylene polymerization in the presence of modified methylaluminoxane (MMAO).

Alternating copolymerization of carbon dioxide and propylene oxide catalyzed by (R,R)-SalenCo(III)-(2,4-dinitrophenoxy) and Lewis-basic cocatalyst

A binary catalyst system of a chiral (R,R)-SalenCo(III)(2,4-dinitrophenoxy) (salen = N,N-bis(3,5-di-tert-butylsalicylidene)-1,2-diphenylethylenediimine) in conjunction with (4-dimethylamino)pyridine (DMAP) was developed to generate the copolymerization of carbon dioxide (CO2) and racemic propylene oxide (rac-PO). The influence of the molar ratio of catalyst components, the operating temperature, and reaction pressure on the yield as well as the molecular weight of polycarbonate were systematically investigated. High yield of turnover frequency (TOF) 501.2 h(-1) and high molecular weight of 70,400 were achieved at an appropriate combination of all variables. The structures of as-prepared products were characterized by the IR, H-1 NMR, C-13 NMR measurements. The linear carbonate linkage, highly regionselectivity and almost 100% carbonate content of the resulting polycarbonate were obtained with the help of these effective catalyst systems under facile conditions.

Thia-michael addition reactions in water using 3-[Bis(alkylthio) methylene]pentane-2,4-diones as odorless and efficient thiol equivalents

3-[Bis(ethylthio)methylene]pentane-2,4-dione (1a) and 3-[bis(benzylthio)methylene]pentane-2,4-dione (1b) have been investigated as non-thiolic and odorless thiol equivalents in thia-Michael addition reactions. In the presence of aqueous p-dodecyl benzenesulfonic acid (DBSA), compound (1) was cleaved and the generated thiols underwent facile conjugate addition to alpha,beta-unsaturated ketones 2 in-situ, affording the corresponding beta-keto sulfides (3) in good yields.

Supramolecular isomerism in zinc hydroxide coordination polymers with pyridine-2,4-dicarboxylic acid: Two polymorphs with centrosymmetric two-dimensional and acentric three-dimensional coordination networks

Reactions of Zn(BF4)(2) and pyridine-2,4-dicarboxylic acid (2,4-pydcH(2)) in the presence of 1,2-bis( 4-pyridyl) ethylene or 1,3-bis(4-pyridyl) propane under hydro(solvo) thermal conditions yielded two polymorphic metal-organic coordination polymers formulated as Zn-2(OH)(2)(2,4-pydc) (1 and 2). Polymorph 1 features a two-dimensional (2-D) layer-like structure that is constructed by 2,4-pydc ligands bridging between the Zn-OH-Zn double-chain units. Each single Zn-OH-Zn chain is composed of mu(2)-OH groups connecting trigonal bipyramidal and tetrahedral Zn centers. Polymorph 2 is a 3-D coordination polymer containing 2-D Zn-OH-Zn sheets that consist of mu(2)- and mu(3)-OH groups and trigonal bipyramidal Zn centers. The sheets are pillared by 2,4-pydc ligands to form an acentric structural architecture. 1 and 2 are rare examples that the two polymorphs exhibit a centrosymmetric 2-D coordination network and an acentric 3-D coordination network, respectively. The different structures lead to differences in photoluminescent properties and thermal stabilities for 1 and 2.