957 resultados para dauciform roots


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维生素(Vitamin)又称维他命,为“万年青”产品,是维持人体生命健康必需的一类低分子有机化合物质。维生素对人体健康的作用人们研究很多, 维生素可以增强人体对感染的抵抗力,降低出生缺陷及降低癌症和心脏病发病率等,一旦缺乏,肌体代谢就会失去平衡,免疫力下降,各种疾病,病毒就会趁虚而入;而维生素对作物影响的研究却很少。目前为止,尚无对用维生素浸种的方法来研究外源维生素是否对小麦种子萌发及幼苗生长起调节作用的报道,且对其在小麦抗逆性方面影响的研究甚少,对盐的胁迫抗性研究尚未有人报道。小麦(Triticum aestivum L.)属于拒盐的淡土性作物。盐害不利于小麦生长,严重影响小麦的产量和品质。本研究采用4 种不同维生素VB1、VC、VB6、VPP,分别对供试小麦品种川育12(红皮)、川育16(白皮)小麦浸种后,在一般自然条件下和逆境(盐胁迫条件)下,进行试验。探讨在正常情况下与在不同盐浓度条件下,各维生素及盐浓度对小麦发芽及幼苗生长的影响,并且比较两种不同皮色的小麦在相同盐胁迫条件下的差异表现,同时研究维生素处理的特异性,且哪种维生素对盐害缓解作用最佳。研究结果表明:在无盐胁迫(自然)条件下,对用4 种不同维生素VB1、VC、VB6、VPP 浸种小麦川育12、川育16 后的种子萌发及幼苗生长(幼苗的根长、根重、苗高、苗鲜重)的研究结果表明:4 种外源维生素浸种均对小麦发芽有调节作用,都能提高其最终发芽率。但是提高幅度有所差异。用VB6 浸种后的小麦提高幅度最多,VC 次之,VPP 提高幅度最小。同时,4 种外源维生素浸种对小麦种子的出芽速度及芽后长势也有一定的影响。VB6、VC 处理的小麦种子出芽速度最快,萌发后长势最好;VB1 出芽速度相对较慢,VPP 最慢,但都大于对照;VB1 处理长势略高于对照,VPP 处理的小麦长势则低于对照。从整体来看,VB6、VC处理促进效应明显, VB1 次之,而VPP 在某些方面无效甚至产生负效应。此外,相同的维生素处理对不同的品种的种子萌发、生长效果也存在差异,各种维生素作用于川育12 的效应均强于对川育16。进一步对幼苗根系TTC 还原力及幼苗叶片中硝酸还原酶活性进行测定、分析。研究发现:并非所有种类的维生素对幼苗根系TTC 还原力及幼苗叶片中硝酸还原酶活性的提高都有帮助。幼苗根系TTC 还原力在不同维生素处理下存在显著差异,而与小麦品种关系甚微。经VB6、VC 处理后,根系TTC 还原力测定值均显著高于对照,VB1 不明显,VPP 则略低于对照。VB6、VC 处理的幼苗叶片中硝酸还原酶的含量大于对照,VB1 与对照相差无几,而VPP 处理的川育12 幼苗叶片中的硝酸还原酶活性比对照CK 略高,而在川育16 中则略比对照CK 有所下降,呈现出抑制效应。综上结果表明:VB6、VC 具有促进种子发芽,幼苗生长及根系生长的作用,是较好的促生长剂;VPP 具有抑制作用,是较好的抑制剂,可进一步研究、开发利用。在盐胁迫条件下,对用4 种不同维生素VB1、VC、VB6、VPP 浸种川育12、川育16 后的种子萌发及幼苗生长(幼苗的根长、根重、苗高、苗鲜重)的研究结果表明:在不同盐浓度胁迫条件下, 各处理的种子萌发及幼苗生长均受到不同程度的抑制。随着盐浓度的增加, 发芽率、发芽指数和活力指数成下降趋势;幼苗的根长、根重、苗高、苗鲜重不断降低。4 种维生素处理间也表现出较大差异。VB6、VC 在每个处理中均保持对盐害的缓解作用,VB6 较VC 更易于促进发芽及幼苗生长。最终发芽率高,根系多、长、重,苗高高、重。而VB1、VPP 则表现出抑制作用。在高盐浓度150mM 时,4 种维生素浸种后的种子,其最终发芽率均不能达到40%,但VB6、VC 处理最终发芽率、苗重、根重均高于对照,VPP 最终发芽率、苗重、根重均低于对照。进一步对幼苗根系TTC 还原力及幼苗叶片中脯氨酸含量进行测定、分析。研究发现:不同盐浓度,不同维生素处理、不同品种间存在差异。随着盐浓度的增加(75mM,100mM,150mM),幼苗根系TTC 还原力活性成下降趋势,幼苗叶片中脯氨酸的积累量成上升趋势。VB6 处理脯氨酸含量增加最为明显,VC 次之,VPP 与对照接近,其变化幅度最小。经VB6、VC 处理后的幼苗根系还原强度,在不同盐浓度下,测定值均显著高于对照,VB1 不明显,VPP 则低于对照,产生负效应。此外,品种间表现不尽相同,相同的维生素处理,相同的盐浓度对不同的品种的种子萌发、生长效果也存在差异, 4 种维生素对川育16 的作用均强于川育12,但其影响趋势是一致的。说明VB6、VC 具有耐(抗)盐性,可以促进种子发芽和幼苗生长,是较好的耐(抗)盐拌种剂。 Vitamin is one kind of necessary low molecular compound for humans tosustain health and life. Lots of Studies have been done on the effectc of the vitaminsfor people. Vitamin can help people improve the body's natural resistance to disease,Drop the rate of birth defects、cacers and the incidence of the heart diseases. Ifpeople have less of them, the metabolism of the organism may throw off balance,immunity may drop off, and catch disease; Though the effects for Vitamin to thecrops are limited. up to now, there’s no one use soking seeds of wheats with vitaminsas a method, to study on how the effects will happen on the wheat seed germinationand seedling growth, and there are only few reserches on antireversion force forwheats ,none for the antireversion force in Sault stress condition.Wheat(Triticum aestivum L.)is sensitive to the salt, so the salt damage will doharm to wheat’s growth, it will have an unfavorable impact on the output and thequality of wheat.On this reaserch, we Soaking CHY12(red)、CHY16 (white) wheat seeds withVitamin C, B1, PP, B6 (50mg/L) as a pretreatment first. Then under two condition: one is in the normal environment the other is in different Salinity, we begin ourexperiments. Then disscuss on if the vitamin and salinity affect the wheat seedgermination and seedling growth, and what is the different between the two of them,the result shows that:Under the normal condition, after soaking seeds with VB1、VC、VB6、Vpp,we study on the their seed germination and the seeding growth(the root length andweights, The seedling heights and weights), it shows that all of those four kinds ofvitamin can adjust the seed germination, but different in The growth rate. VB6 isbest for increase, VC comes second,VPP is the worst. Meanwhile, those four vitaminalso have effect on the speed of the sprouting of the wheat. VB6、Vc can faster theseed germination most, and the seedlings are all doing well; VB1 do little effects onthe budding, Vpp is the worst, but all treatments are better than CK; but in Vi, VB1some what above the CK, while VPP lower than that. On the whole, the acceleratingeffect of VB6、VC are obvious, VB1 takes second place, but VPP in some aspects arenoneffective even have negative effect. Furthermore, different kind of seeds with thesame vitamin may different in seed germination and seedling growth, four vitaminson CHY16 is better than CHY12.More studies on TTC reductive capacity of roots and the activity of nitratereductase in the leaves, the reasult shows not all the vitamin can help the seedlings toimprove the TTC reductive capacity and the activity of nitrate reductase. TTCreductive capacity in different treatments shows significant differences,but notcorrelate to the variety of the wheat. The TTC reductive capacity of VB6、Vctreatments are all higher than CK, VB1 is nearly the same as CK, VPP is a littlelower than CK. Through the study of acivity of nitrate reductase, it shows that,VB6、VC are higher than CK ,VB1 is nearly the same as CK also, VPP is a little higher inthe CK of CHY12 but lower in CHY16. Through all the results above: VB6、Vc helpthe wheat seed germination, seedling growth and the growth of roots, is theperfectable factor of stimulating the growth; Vpp is a inhibition, that’ll be furtherreserch,and well develop and utilize in the future.Under the different Salinity condition, after soaking seeds with VB1、VC、VB6、Vpp,we study on the their seed germination and the seeding growth(the root lengthand weights, The seedling heights and weights), it shows that: under differentsalinity, the seed germination and the seedling growth of any treatment are inhibited.With the increase of the concentration, the germination rate, Vi、Gi all had fallen; theroot length and weight, the seedling heights and weights steadily sank down. There are also have pronounced difference between all treatments with four differentvitamins.VB6、VC in all treatments are alleviative the salt damage, VB6 is easier tocause to put forth buds than VC, and it’s quantitative value is the highest in theultimate germination rate, in root and seedlings’ hight and weight. Though the VPP、VB1 are seems to inhibite its growth. Under the high concentration150mM Nacl, theultimate germination rate in all treatments are below the 40%, but VB6、VC’squantitative values in any experiments are higher than CK,while VPP lower thanCK.Then we study on the TTC reductive capacity of roots and the content of Polinein leaves, the result shows that between the different salinity, different vitamintreatments, different varieties of the wheat have discrepancy.along with theincreasing concentraion of the salinity(75mM,100mM,150mM),TTC reductivecapacity of roots decreases, the accumulation of the content of Poline in leaves havean upward trend. The increase of VB6’s treatment are obviously, VC comessecond,VPP is nearly come up with CK, changes a little. In TTC reductive capacity of roots’s reserch, VB6、VC are higher than CK at any time,VB1 is not palpable,VPP is lower than CK, makes negative affect on wheat. In addition, varieties of thewheats are remain different, no matter it shows promoting or inhibiting, all fourvitamins have moreobvious effects on CHY16 than CHY12, but the tendency of theeffection are the same. It is say that VB6、VC can help wheat to standwith the saultwell, and promot in growth,they are the better reagent to mix with the seed.

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禾谷孢囊线虫严重影响禾谷类作物的产量,在小麦中由禾谷孢囊线虫引起的产量损失可达30-100%。尤其在澳大利亚、欧洲、印度和中东危害严重,目前禾谷孢囊线虫已成为危害我国作物的主要病源。控制禾谷孢囊线虫的方法主要有:作物轮作、杀线虫剂、寄主抗性等等,其中基因工程方法培育抗线虫小麦品种被认为是最经济有效的方法。分离抗禾谷类孢囊线虫基因对揭示抗性基因结构与功能及其表达调控具有重要意义。 尽管小麦是重要的粮食作物,在小麦中已发现的抗禾谷孢囊线虫的基因很少,而比其近缘属如节节麦、易变山羊草、偏凸山羊草中含有丰富的抗源。目前已鉴定出禾谷孢囊线虫抗性位点Cre,并发现了9个禾谷孢囊线虫抗性基因(Cre1,2, 3, 4, 5, 6, 7, 8, and R) ,其中只有Cre1和Cre8直接从普通小麦中获得。从节节麦中获得的Cre3基因能最有效的控制线虫数量,其次是Cre1和Cre8。这些基因的克隆对于了解禾谷孢囊线虫抗性机制及进一步的育种应用都是非常关键的。然而,目前为止仅有Cre3基因通过图位克隆的方法从节节麦中被分离得到。该基因已被克隆得到的多数线虫抗性基因一样均属于核苷酸结合位点区(NBS)-亮氨酸重复序列区(LRR)基因家族。目前,已有很多抗性基因被分离,这些已知的NBS-LRR类抗性基因的保守序列为应用PCR的方法克隆新的抗性基因提供了可能。 因此本课题的目的是采用保守区同源克隆、3′RACE 和5′RACE 等方法从抗禾谷孢囊线虫小麦-易变山羊草小片段易位系E10 中克隆小麦抗禾谷孢囊线虫基因全序列,进而通过半定量PCR 和荧光定量PCR 研究该基因的表达模式。同时通过mRNA 差别显示技术和任意引物PCR(RAP-PCR)技术分离克隆植物禾谷孢囊线虫抗性基因及其相关基因,为阐明植物抗病性分子机制以及改良作物抗病性和作物育种提供基础,为通过分子标记辅助育种和基因工程方法实现高效、定向转移抗病基因到优良小麦品种奠定了重要的理论和物质基础。主要研究结果: 1. 本实验根据此前从抗禾谷孢囊线虫材料E-10 扩增得到的与来自节节麦的抗禾谷孢囊线虫Cre3 基因及其他的NBS-LRR 类抗性基因的NBS 和LRR 保守区序列设计了两对特异性引物,从E10 中扩增到532bp 和1175bp 的两个目标条带,它们有一个32bp 的共同序列,连接构成总长为1675bp 的NBS-LRR 编码区(命名为RCCN)。根据RCCN设计引物,利用NBS-LRR区序列设计引物,通过5′RACE 和3′RACE 技术采用3′-Full RACE Core Set(TaKaRa)和5'-Full RACE Kit (TaKaRa)试剂盒,反转录后通过嵌套引物GSP1 和GSP2 分别进行两轮基因特异性扩增,分别将NBS_LRR 区向5′端和3′端延伸了1173bp 和449bp,并包含了起始密码子和终止密码子。根据拼接的得到的序列重新设计引物扩增进行全基因扩增的结果与上面获得的一致。拼接后得到全长2775 bp 的基因序列(记作CreZ, GenBank 号:EU327996)。CreZ 基因包括完整的开放阅读框,全长2775 bp,编码924个氨基酸。序列分析表明它与已知的禾谷孢囊线虫抗性基因Cre3的一致性很高,并且它与已经报到的NBS-LRR 类疾病抗性基因有着相同的保守结构域。推测CreZ基因可能是一个新的NBS-LRR 类禾谷孢囊线虫抗性基因,该基因的获得为通过基因工程途径培育抗禾谷孢囊线虫小麦新品种奠定了基础,并为抗禾谷孢囊线虫基因的调控表达研究提供了参考。 2. 通过半定量PCR和SYBR Green荧光定量PCR技术对CreZ基因的相对表达模式进行了研究。以α-tubulin 2作为参照,采用半定量PCR 分析CreZ 基因在不同接种时期1d, 5d, 10, 15d 的E-10的根和叶的的表达情况。在内参扩增一致的条件下,CreZ 在E-10的根部随着侵染时间的增加表达量有明显的增加,在没有侵染的E-10的根部其表达量没有明显变化,而在叶中没有检测表达,说明该基因只在抗性材料的根部表达。SYBR Green定量PCR分析接种前后E10根部基因CreZ基因的表达水平为检测CreZ基因的表达建立了一套灵敏、可靠的SYBRGreen I 荧光定量PCR 检测方法。接种禾谷孢囊线虫后E10根内CreZ基因的相对表达水平显著高于接种前。随接种时间的延长持续增加,最终CreZ基因的相对表达量达到未接种的对照植株的10.95倍。小麦禾谷孢囊线虫抗性基因CreZ的表达量与胁迫呈正相关,表明其与小麦的的禾谷孢囊线虫抗性密切相关,推测CreZ基因可能是一个新的禾谷孢囊线虫候选抗性基因。 3. 针对小麦基因组庞大、重复序列较多,禾谷孢囊线虫抗性基因及其相关基因的片断难以有效克隆的问题,通过mRNA 差别显示技术及RAP-PCR 技术分离克隆植物禾谷孢囊线虫抗性及其相关基因。试验最终得到154 条差异表达条带,将回收得到的差异条带的二次PCR 扩增产物经纯化后点到带正电的尼龙膜上,进行反向Northern 杂交筛选,最终筛选得到102 个阳性差异点。将其中81 个进行测序,并将序列提交到Genbank 中的dbEST 数据库,分别获得登录号(FE192210 -FE192265,FE193048- FE193074 )。序列比对分析发现,其中26 个序列与已知功能的基因序列同源;有28 条EST 序列在已有核酸数据库中未找到同源已知基因和EST,属新的ESTs 序列;另外27 个EST 序列与已知核酸数据库中的ESTs 具有一定相似性,但功能未知。其所得ESTs 序列补充了Genbank ESTs 数据库,为今后进一步开展抗禾谷类孢囊线虫基因研究工作打下了基础。结合本试验功能基因的相关信息,对小麦接种禾谷孢囊线虫后产生的抗性机制进行了探讨。接种禾谷孢囊线虫后植物在mRNA 水平上的应答是相当复杂的,同时植物的抗病机制是一个复杂的过程,涉及到多个代谢途径的相互作用。 The cereal cyst nematode (CCN), Heterodera avenae Woll, causes severe yieldreductions in cereal crops. The losses caused by CCN can be up to 30-100% in somewheat fields. At present, cereal cyst nematode has become the major disease sourcein China and it also damaged heavily in Australia, Europe, India and Middle East.The damage caused by CCN can be mitigated through several methods, includingcrop rotation, nematicide application, cultural practice, host resistance, and others.Of these methods, incorporating resistance genes into wheat cultivars and breedingresistant lines is considered to be the most cost-effective control measure forreducing nematode populations. Although wheat is an economically important crop around the world, far fewergenes resistant to CCN were found in wheat than were detected in its relatives, suchas Aegilops taucchi, Aegilops variabilis and Aegilops ventricosa. Cloning these genesis essential for understanding the mechanism of this resistance and for furtherapplication in breeding. Because of the huge genome and high repeat sequencescontent, the efficient methods to clone genes from cereal crops, are still lacking. A resistance locus, Cre, has been identified and 9 genes resistant to CCN (designatedCre1, 2, 3, 4, 5, 6, 7, 8, and R) have been described, in which Cre1 and Cre8 werederived directly from common wheat. The Cre3 locus, which was derived from Ae.tauschii, has the greatest impact on reducing the number of female cysts, followed byCre1 and Cre8. Cloning these genes is essential for understanding the mechanism ofthis resistance and for further application in breeding. However, to this point, only Cre3, a NBS-LRR disease resistance gene, has been obtained through mappingcloning in Ae. tauschii. The majority of nematode resistance genes cloned so far belong to a super familywhich contains highly conserved nucleotide-binding sites (NBS) and leucine-richrepeat (LRR) domains. To date, many NBS-LRR resistance genes have been isolated.The conserved sequences of these recognized NBS-LRR resistance genes provide thepossibility to isolate novel resistance genes using a PCR-based strategy. The aim of the present study was to clone the resistance gene of CCN fromWheat/Aegilops variabilis small fragment chromosome translocation line E10 whichis resistant to CCN and investigate the espression profiles of this gene withsemi-quantitative PCR and real-time PCR. Another purpose of this study is cloningthe relational resistance gene for CCN by mRNA differential display PCR andRAP-PCR. These works will offer a foundation for disease defence of crop andbreeding and directional transferring resistance gene into wheat with geneengineering. Primary results as following: 1.According to the conversed motif of NBS and LRR region of cereal cystnematode resistance gene Cre3 from wild wheat (Triticum tauschlii) and the knownNBS-LRR group resistance genes, we designed two pairs of specific primers for NBSand LRR region respectively. One band of approximately 530bp was amplified usingthe specific primers for conversed NBS region and one band of approximately 1175bpwas amplified with the specific primers for conversed LRR region. After sequencing,we found that these two sequences included 32bp common nucleotide having 1675bpin total, which was registered as RCCN in the Genbank. Based on the conservedregions of known resistance genes, a NBS-LRR type CCN resistance gene analog wasisolated from the CCN resistant line E-10 of the wheat near isogenic lines (NILs), by5′RACE and 3′ RACE.designated as CreZ (GenBank accession number: EU327996) .It contained a comlete ORF of 2775 bp and encoded 924 amino acids. Sequencecomparison indicated that it shared 92% nucleotide and 87% amino acid identitieswith those of the known CCN-resistance gene Cre3 and it had the same characteristic of the conserved motifs as other established NBS-LRR disease resistance genes. 2. Usingα-tubulin 2 as exoteric reference, semi-quantitative PCR and real-timePCR analysis were conducted. The expression profiling of CreZ indicated that it wasspecifically expressed in the roots of resistant plants and its relative expression levelincreased sharply when the plants were inoculated with cereal cyst nematodes. therelative expression level of the 15days-infected E10 is the 10.95 times as that ofuninfected E10,ultimately. It was inferred that the CreZ gene be a novel potentialresistance gene to CCN. 3.We cloned the relational resistance gene for CCN by mRNA differentialdisplay PCR and arbitrarily primed PCR fingerprinting of RNA from wheat whichpossess huge and high repeat sequence content genomes. Total 154 differentialexpression bands were separated and second amplified by PCR. The products werenylon membrane. The 102 positive clones were filtrated by reverse northern dot blotand 81 of those were sent to sequence. The EST sequences were submitted toGenbank (Genbank accession: FE192210 - FE192265, FE193048 - FE193074). Thesequences alignment analysis indicated 26 of them were identical with known genes;28 were not found identical sequence in nucleic acid database; another 27 ests wereidentical with some known ests, but their functions were not clear. These ESTsenriched Genbank ESTs database and offered foundation for further research ofresistance gene of CCN.

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The effect of different nitrogen and phosphorus sources on pH and the availability of mineral nutrients in the root/soil interface of Larix gmelinii seedlings were studied by means of root-mat method. The results showed that the addition of NH~+_4-N decreased the pH in the root/soil interface, while the addition of NO~-_3-N increased the pH in contrast with the control treatment. The sort of the P sources and the distance from the root plane remarkably influenced the changes of pH in the root/soil interface induced by the addition of the nitrogen sources. Compared with the addition of only NH~+_4-N, the extent to which the pH in the root/soil interface decreased was obviously smaller when treated by NH~+_4-N and rock P. When treated with different P sources, the contents of available P in the root/soil interface were affected by the sort of the N sources. When treated with soluble P, the contents of the available P in the root/soil interface obviously increased for the addition of both NH~+_4-N and NO~-_3-N. When treated with rock P, the contents of the available P increased only in the area 0~3 mm from the root plane for NH~+_4-N, whereas the contents of available P in the root/soil interface changed little for NO~-_3-N. The results above showed that the protons excreted by the roots were the main driving force for the solution of the rock P in the root/soil interface. The availability of Fe in the root/soil interface increased as a result of acidity induced by the NH~+_4-N, whereas the availability of Fe in the root/soil interface decreased because of the pH increase induced by the NO_3~-_N. The effect of different N sources on the availability of Fe in the root/soil interface was also affected by the sort of P sources. The concentrations of P、Fe in the leaves remarkably differed when treated by different N、P sources and concentrations of the P、Fe in the root/soil interface were correlated to those in the leaves of the seedlings.

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Phyllospadix iwatensis Makino and phyllospadix japonicus Makino have similar frunt morphology and anatomy.The rhomboid fruit of Japanese phyllospadix is dark brown in colour and is characterized by two arms bearing stiff inflected bristles which can act as an anchoring system. The fruit covering consists of a thin cuticular seed coat and pericarp remains mainly fibrous endocarp. In the groove region of the fruit.the cuticular seed coat and endocarp are replaced by nucellus cells with wall in growths and crushed pigment strands with lignified walls.these tissues appera to control the transfer of nutrients to developing seed.the seed is oval with a small embryo and a large hypocotyl. the embryo is straight and simple,with the plumule containing three leaf primordia and a pair of root primordia surrounded by a cotyledon.the hypocotyl has large vontral lobe containing central provascular tissue and two small dorsal lobes.the hypocotyl contains starch.lipid and protein.and acts as a nutrient store.the seed of P.iwatensis has a dormancy period of 2-6 weeks and germination eventually reaches-65%.but is not synchronized.during germination the leaves emerge first.and then after at least three young leaves have formed and abseised.the roots emerge,usually?6 months after the commencement of germination.Utilizaton of the nutrient reserves is initially from the perihpery of the hypocotyl and then progressively towards its centre.

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采用盆栽试验基于统计学方法,对4种不同品种小麦在4个连续生长期根系表层土壤(0~20cm)化感潜势时空异质性进行了研究。结果表明:不同品种小麦之间根系土壤化感潜势差异极显著(P=0.01),随生育期变化,化感潜力的变异与品种有关,一般15cm为普通小麦耕层土壤化感潜力的转折位点。变异函数分析显示,4种小麦根系土壤化感潜势变化是独立、随机、异质性的。"碧玛1号"、"丰产3号"、"宁冬1号"、"小偃22号"变异函数理论模型分别为线形模型、球型模型、指数模型和高斯模型。其中"小偃22号"的化感背景值和化感潜力空间结构比随生育期增大,导致0~20cm表层土壤化感表达具有高度的空间异质性。4种普通小麦的化感表达均存在时空异质性,其中"宁冬1号"的表层土壤化感表达具有很好的分形特征,其空间分布格局的变异存在尺度依赖。"宁冬1号"化感潜势在表层土壤的空间分布趋于离散表达,化感潜力的有效纵向半径和有效延深半径分别为5cm和14cm。这种时空变异格局可能与根系发育特征、根系翻转运动及土壤环境有关,化感实施过程可能为熵增过程。根系表层土壤化感潜势时空异质性的研究可为监测化感作用实施,定位有效化感物质和合理利用土壤化感潜势提供理论...

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在遮雨棚控水条件下,采用盆栽的方式研究了不同秸秆覆盖量对玉米根、冠生长的影响。试验按对照(CK)和秸秆覆盖量0.3 kg/m2(SM0.3)、0.6 kg/m2(SM0.6)、0.9 kg/m2(SM0.9)、1.2 kg/m2(SM1.2)共设5个处理,水分按高水(占田间持水量的90%)和低水(占田间持水量的60%)设两个水平。分别测定了玉米根、茎、叶、穗干重,根系垂直空间分布及叶片叶绿素相对含量等指标。结果表明:秸秆覆盖明显改变了玉米根系和地上部分的生长;高水条件下SM0.6处理玉米根系、茎秆、叶和穗干重均高于其它处理;低水条件下,地上部分干重SM1.2最大,SM0.6次之;根系的垂直空间分布与水分和覆盖条件都有密切的关系,覆盖措施主要影响下层根系的生长和发育。

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利用长期定位试验资料,研究了黄土高原丘陵沟壑区乔木和灌木植物系数的计算方法,比较了两种代表性乔木(榆树和小叶杨)和两种代表性灌木(柠条和沙棘)的实际蒸散量和生育期土壤平均含水量的差异,分析了土壤含水量变化对植物根系吸水和土壤水分有效性的影响。结果发现:该地区灌木的实际蒸散量小于乔木,但同类植物的实际蒸散量没有显著差异;土壤含水量柠条最高,沙棘最低;榆树植物系数最小,柠条其次,沙棘最大,但榆树和小叶杨的土壤水分有效性高,耗水量大,所以灌木较适于该区生长。

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通过调节B5培养基中的组分,研究了金钩南瓜组培根在五种营养元素(P、Mg、Fe、Cu、B)四个浓度梯度(1/2 B5、B5、3/2 B52、B5)培养下化感作用的响应模式以及对黑籽和金钩南瓜两种受体幼苗生长的影响。结果表明:不同营养元素对受体植物幼苗生长的影响不一致,与元素含量显著相关,而且依赖于受体选择。五种营养元素在亏缺(1/2 B5)和正常(B5)条件下南瓜组培根过滤液对受体植物幼苗生长均表现为抑制作用;而适量增加营养元素的条件下(3/2 B5和2 B5),一般表现为促进作用,但2 B5含量下,B元素导致金钩南瓜的自毒作用,而Fe能引发金钩南瓜组培根过滤液对黑籽南瓜的抑制作用。因此理论上初步得出P和Mg元素可以降低南瓜根系的毒害作用,而Fe、Cu和B元素对南瓜根系的化感调控作用与品种选择有关,这对调控施肥、降低设施农业中葫芦科作物的连作障碍具有一定的参考意义。

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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...

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以陕北农牧交错带人工草种紫花苜蓿(Medicago sativa L.)和天然草种短花针茅(Stipa breviflora Griseb.)为对象,采用根钻法调查两个草种的根系垂直分布以及刈割后苜蓿根系变化特征,并通过定位观测研究土壤水分动态变化。结果表明:紫花苜蓿和短花针茅根系密度随土壤深度增加而减少,而且均以直径小于等于1 mm的须根为主;0~50 cm土层紫花苜蓿和短花针茅根系量分别占0~100 cm剖面总量的67%和84%。紫花苜蓿和短花针茅根系分布与土壤水分消耗特征吻合。生长旺盛期苜蓿大量消耗0~140 cm土层土壤水分,5-9月平均有效土壤储水不足10 mm;生长季末深层(140~280 cm)土壤储水也逐渐降低,约为裸地储水量的50%。短花针茅0~280cm剖面土壤水分状况明显好于苜蓿地,比苜蓿地多储水100 mm左右;主要消耗浅层(0~50 cm)土壤水分,深层水分利用较少。

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通过喷灌玉米田间试验,研究了喷灌水经玉米冠层再分配后的分布状况。结果表明:在玉米全生育期,茎秆下流水量占灌水量的均值为44%左右,棵间穿透水量占灌水量的均值为48%左右,冠层截留量在0.8 ̄2.9mm之间变化。一次灌水中,喷灌水在地表的分布很不均匀,43.2%的灌水量经茎秆下流到根区,在距离茎秆7cm,15cm,25cm和32.5cm处,地表接收的水量占总灌水量的比例分别为18.9%、43.5%、66.9%和84.5%。灌水量、种植密度、株高和叶面积指数等都影响着喷灌水在地表的分布。

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植物根系除支撑和固定其地上部这一力学功能外的一个重要功能就是从土壤中吸收水分和养分以满足植物地上部生长所需.表征植物根吸水能力的一个重要的水力学参数是水力导度(用单位时间单位面积的水流速率来表示),可在细胞(细胞水力导度)、单根和整株根系水平上来表达,其中单根导度可分为径向导度和轴向导度,仅径向导度反映了单根吸收水分的能力,而轴向导度则反映了植物根系输导水分的能力,但在整株根系水平上则以通过整个根系的水流通量与根木质部和根表土壤间的水势差之比来表示,既包括径向导度也包括轴向导度.近年来,对植物根系吸水或根水力导度研究已取得了许多重要进展,这对阐明根系吸水机理和地上地下部关系起到了重要作用.下面做一简要综述.1 根系吸收水分的主要部位根系吸水的部位一般认为在距根尖10~100mm的区域内,这种看法是基于解剖上的证据.从根表面到根中心,依次为根表皮、下表皮、皮层、内皮层、中柱,其中根表皮是有最高吸收活性的根区,但一般仅可存活几天,而内皮层将皮层和中柱分开形成了根内侧的一个界面,老根一般有周皮或栓质化的内皮层,有很强的不透水性(即阻力很大).但Sanderson[1]对大麦的研究发现,虽然老根区内重度栓化的内皮层已...

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为诱导无芽黄精根状茎产生不定芽,选择不同的化学物质进行诱导处理。结果表明,GA3处理效果明显,选用0.4 mg/L的GA3浸泡25 min对黄精根状茎不定芽的产生和须根生长有明显促进作用,高浓度抑制其生长;1%硫脲浸泡处理对黄精无顶芽根状茎萌发新芽和须根有明显的抑制作用。

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研究了黄土区不同演替阶段草地植被细根垂直分布特征与土壤环境的关系,结果表明不同演替阶段草地植被细根生物量、根长密度、表面积、直径和比根长均具有明显的垂直分布特征。细根生物量、根长密度和细根表面积一般随土层加深而逐渐减少,且集中分布于0~40cm土层;随着演替的进行,除20a弃耕地外,0~80 cm土层细根生物量、根长密度和细根表面积逐渐增加;除25a弃耕地外,细根直径随演替进行逐渐减小。0~100 cm土层土壤含水量随演替进行而增加,不同演替阶段深层土壤水分较表层稳定。土壤容重的变化趋势为9<4<15<20<25a弃耕地,根系对表层土壤水分和容重的影响较大,而对深层土壤水分与容重影响较少。不同演替阶段细根各参数和土壤水分、容重差异均达到显著水平。各弃耕地细根参数之间,细根参数和土壤环境因子之间存在不同程度的相关关系,土壤含水量在草本植被的不同演替阶段均是影响其细根垂直分布的关键因素。土壤容重在演替早期对草本植被根系的影响较小,随着演替进行其影响作用进一步增强。

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The results of the examination showed that some wetland plants' leaves and stems above the surface of water have little ability to supply water body with oxygen through roots of themselves while they are photosynthesizing. These plants are calamus(Acorus calamus), cattail(Typha angustifolia), wild rice stem(Zizania caduciflora), Cyoerus alternifokius, and water hyacinth(Eichhornia crassipes). It means that there is no relationship between these plants' photosynthesis and the breath of root cells. But duckweed(Lemna minor) has a small to raise DO 0.44mg·L -1 in average, while it is photosynthesizing during the examination. Reed(Phragmitas communis) may have a little the to provide oxygen for water body through root of itself while it is photosynthesizing. It raised DO 0.30mg·L -1 in average during the examination.