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谷子全生育期抗旱性鉴定及抗旱指标筛选 总被引:13,自引:0,他引:13
作物全生育期抗旱性对发掘和利用抗旱品种和抗旱基因至关重要,但谷子全生育期抗旱鉴定至今未有报道,抗旱鉴定缺乏鉴定指标。本试验在干旱池模拟干旱条件下,对苗期抗旱性表现不同的谷子品种进行了全生育期抗旱性研究,调查分析了根干重等形态和生理性状在干旱胁迫条件下的变化;采用相关和灰色关联度等方法,分析这些指标与抗旱性(DRI)的关系。结果表明,相对根冠比、相对单穗粒重和灌浆期光合速率、蒸腾速率同抗旱性表现极显著相关,可以作为谷子全生育期抗旱性鉴定的指标;而相对根干重、相对单穗重、相对株高和气孔导度则可以作为谷子全生育期抗旱性鉴定的参考指标;在供试的品种中,红根谷和大齐头白表现了良好的综合抗旱性。本文还讨论了抗旱性的复杂性以及不同性状对干旱胁迫的反应,所建立的指标对谷子全生育期抗旱鉴定具有指导意义。 相似文献
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高羊茅叶片表皮蜡质含量与其抗旱性的关系 总被引:2,自引:0,他引:2
以14个高羊茅品种为试验材料,在田间试验中对干旱高温胁迫下的叶片表皮蜡质含量、净光合速率、蒸腾速率、气孔导度、胞间CO2浓度等生理指标测定分析。结果表明,干热胁迫下高羊茅品种间的叶片表皮蜡质含量和水分利用效率均存在极显著差异(P<0.01);叶片蜡质含量与综合抗旱性和水分利用效率的等级相关系数分别为0.78(P<0.01)和0.68(P<0.01);蜡质含量越高的品种,其叶片气孔导度和胞间CO2浓度越低,水分利用效率越高,但所有品种的水分利用效率绝对值都较低。研究发现,在干热胁迫时,高羊茅叶片表皮蜡质可通过对气孔导度的调节来减少气孔蒸腾,提高水分利用效率,最终提高其抗旱性;表皮蜡质含量可以作为高羊茅品种抗旱性鉴定的一个新指标。 相似文献
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谷子孕穗期抗旱指标筛选 总被引:4,自引:0,他引:4
为研究谷子孕穗期在干旱环境的形态、生理、生化性状变化趋势,筛选谷子孕穗期抗旱性鉴定指标,以20个谷子品种为试验材料,在模拟干旱棚中分析了谷子孕穗期干旱胁迫条件下形态和生理、生化指标的变化。试验表明:单穗重、单穗粒重、株高、穗下茎长、千粒重与抗旱指数的相关性显著,可作为孕穗期抗旱性的形态指标;叶绿素含量、可溶性糖、丙二醛含量和超氧化岐化酶活性(SOD)4个指标与抗旱指数的相关性显著,可作为孕穗期的生理、生化指标。通过主成分分析确立了千粒重、单穗重、叶绿素和SOD等4个指标的相对值为谷子孕穗期抗旱性综合指标,以抗旱指数为因变量,4个综合指数为自变量建立的回归方程对供试品种的抗旱性进行预测具有高的准确性。 相似文献
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不同蚕豆品种对铅污染的光合生理响应特征 总被引:3,自引:0,他引:3
以3个蚕豆品种(分别为K0883、K0502、K0697)为试验材料,通过大田模拟小剂量Pb污染(浓度为40和250 mg·kg-1),研究了净光合速率、气孔导度、蒸腾速率、细胞间隙CO2浓度、水分利用效率、叶绿素含量等光合生理响应特征的变化在不同品种中的差异.结果表明,Pb污染下3个蚕豆品种气孔导度和蒸腾速率没有显著变化,叶绿素含量有不同程度的上升;在250 mg·kg-1 Pb浓度下,K0883蚕豆品种净光合速率、水分利用效率、细胞间隙CO2浓度分别升高121.80%、上升193.70%、下降42.76%.3个蚕豆品种对Pb污染的抗性大小顺序为K0883>K0697>K0502.蚕豆不同光合生理指标对小剂量Pb污染的响应特征不同.不同蚕豆品种对小剂量Pb污染的响应特征存在差异,这种种内的差异性采用单个生理指标难以反映,只有通过对多个指标的整合分析才能表现出来. 相似文献
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中国西北干旱区树木蒸腾对气象因子的响应 总被引:14,自引:2,他引:12
应用数值方法 ,对中国西北干旱区 5个主要树种 (樟子松、榆树、二白杨、胡杨和沙枣 )的叶面蒸腾及气孔导度对气象因子的响应进行了探讨 ,时间尺度为日。两套综合环境观测系统分别安置在黑河中游的临泽和下游的额济纳旗 ,每半小时自动记录微气象因子、土壤水分和树汁流量。应用日平均树汁流量、饱和差、总辐射、平均气温和土壤含水量拟合树木叶面蒸腾及气孔导度的经验公式。气孔导度和单个气象因子之间具有很高的相关性。应用多个气象因子所建立的经验公式能够很好的模拟气孔导度 ,模拟效果比气孔导度与单一因子的相关性高。气孔导度总体上和饱和差和气温呈指数关系 ,与总辐射的关系多种多样 ,与土壤含水量的关系较复杂。在中游地区 ,二白杨气孔导度、叶面蒸腾量和单株树木树汁流量最大。试验期间下游试验点土壤水分充足 ,耐旱树种胡杨及沙枣树汁流量较大 ,但其气孔导度及叶面蒸腾量均较小。本次研究没有发现树木叶面蒸腾量和单一环境因子之间具有明显的相关性。叶面蒸腾模拟效果没有气孔导度模拟效果好 ,原因是叶面蒸腾是气孔导度和饱和差的函数。 相似文献
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根系分区灌溉和水分利用效率 总被引:23,自引:2,他引:21
根系分区灌溉是指仅仅部分根系受到正常的灌溉,其余根系则受到人为的干旱,两项理论根据指出这种措施可减少植物的水分肖耗,并保持一定的生物产量,其一是植物蒸腾失水与气孔导性是线性关系,而光合作用与气孔导性则是一种渐趋饱和的关系,如果气孔导性从最大值适应调低,可显著降低蒸腾,但对光合影响应小得多,其二是处于干燥土壤中的根系可感觉干旱,产生干旱信号来调节地上部分的气孔开度,显然,这项措施在田间有多大效用值得深入研究。 先是大田作物的蒸腾失水仅部分地受气孔控制,界面层的扩散阻力起很大作用。因此该措施可能对界面层阻力较小的,如果树等作用大些,另外,根系干旱信号可否“长期”地产生和调控气孔仍需试验证明。 相似文献
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在河西走廊临泽绿洲北部试验区,对春小麦进行3种水分处理并同时观测了全生育期内的蒸发蒸腾(ET)及环境中各生态因子和植物生理指标。结果表明:当年全生育期内,春小麦ET在充分供水条件下为593mm;在中等供水条件下为365mm;在少量供水条件下为280mm。其日蒸散量分别为5.5mm,3.4mm和2.8mm。讨论了影响ET和植物蒸腾的各植物生理指标和环境因子,发现在植物诸指标与蒸腾相关程度的顺序为:叶片水势、气孔导度和叶温(充分供水)及叶片水势、叶温和气孔导度(水分胁迫)。在环境诸因子中与ET的相关程度顺序是:有效光合辐射、净辐射、20cm土温、大气饱和水汽压差,15cm土温、气温、10cm土温、土壤表面温度及5cm土温。 相似文献
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A unique multibranched cyclomaltooligosaccharide (cyclodextrin, CD) of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose [6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin, (G(2))(3)-betaCD] was prepared. The physicochemical and biological properties of (G(2))(3)-betaCD were determined together with those of monobranched CDs (6-O-alpha-D-glucopyranosyl-alpha-cyclodextrin (G(1)-alphaCD), 6-O-alpha-D-glucopyranosyl-beta-cyclodextrin (G(1)-betaCD), and 6-O-alpha-maltosyl-beta-cyclodextrin (G(2)-betaCD)). NMR spectra of (G(2))(3)-betaCD were measured using various 2D NMR techniques. The solubility of (G(2))(3)-betaCD in water and MeOH-water solutions was extremely high in comparison with nonbranched betaCD and was about the same as that of the other monobranched betaCDs. The formation of an inclusion complex of (G(2))(3)-betaCD with stereoisomers (estradiol, retinoic acid, quinine, citral, and glycyrrhetinic acid) depends on the cis-trans isomers of guest compounds. The cis isomers of estradiol, retinoic acid, and glycyrrhetinic acid were included more than their trans isomers, while the trans isomers of citral and quinine fit more tightly than their cis isomers. (G(2))(3)-betaCD was the most effective host compound in the cis-trans resolution of glycyrrhetinic acid. Among the branched betaCDs, (G(2))(3)-betaCD exhibited the weakest hemolytic activity in human erythrocytes and showed negligible cytotoxicity in Caco-2 cells up to 200 microM. These results indicate unique characteristics of (G(2))(3)-betaCD in some biological responses of cultured cells. 相似文献
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Choi DW Do YS Zea CJ McEllistrem MT Lee SW Semrau JD Pohl NL Kisting CJ Scardino LL Hartsel SC Boyd ES Geesey GG Riedel TP Shafe PH Kranski KA Tritsch JR Antholine WE DiSpirito AA 《Journal of inorganic biochemistry》2006,100(12):2150-2161
Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ. 相似文献
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We utilize electrophoresis and find that a thermally treated equimolar mixture of the oligonucleotide d(G(5)T(5)) and its complementary oligonucleotide d(A(5)C(5)) exhibits either two bands or a single band in one lane, depending on the conditions of the incubation solutions. The thermally treated d(G(5)T(5)) solution loaded in a different lane exhibits a single band of the parallel quadruplex [d(G(5)T(5))](4), which is composed of homocyclic hydrogen-bonded G(4) and T(4) tetrads previously proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(A(5)C(5)), the fast band is assigned to a Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex, so that the slow band with the same low mobility as that of [d(G(5)T(5))](4) may be assigned to either [d(G(5)T(5))](4) itself or a [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex. If the latter compound is true, this may be the antiparallel quadruplex composed of the heterocyclic hydrogen-bonded G-C-G-C and T-A-T-A tetrads proposed previously. After removing these three bands for the duplex and two kinds of hypothetical quadruplexes, we electrophoretically elute the corresponding compounds in the same electrophoresis buffer using an electroeluter. The eluted compounds are ascertained to be stable by electrophoresis. The circular dichroism (CD) and UV absorption spectra measured for the three isolated compounds are found to be clearly different. For the electrophoretic elution of the hypothetical [d(G(5)T(5))](4) quadruplex, the result of the molecularity of n = 4 obtained from the CD melting curve analysis provides further support for the formation of the parallel [d(G(5)T(5))](4) quadruplex already proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(C(5)A(5)), the fast band with a molecularity of n = 2 corresponds to the Watson-Crick duplex, d(G(5)T(5)). d(A(5)C(5)). The slow band with a molecularity of n = 4 indicates the antiparallel quadruplex [d(G(5)T(5)). d(A(5)C(5))](2), whose observed CD and UV spectra are different from those of [d(G(5)T(5))](4). By electrophoresis, after reannealing the eluted compound [d(G(5)T(5)). d(A(5)C(5))](2), a distinct photograph showing the band splitting of this quadruplex band into the lower duplex and upper quadruplex bands is not possible; but by a transilluminator, we occasionally observe this band splitting with the naked eye. The linear response polarizability tensor calculations for the thus determined structures of the [d(G(5)T(5))](4) quadruplex, the McGavin-like [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex, and the Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex are found to qualitatively predict the observed CD and UV spectra. 相似文献
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A novel blue‐emitting Sr3.5Y6.5O2(PO4)1.5(SiO4)4.5:Eu2+ phosphor was synthesized via a solid‐state reaction. Powder X‐ray diffraction (XRD) analysis demonstrated that the Sr3.5Y6.5O2(PO4)1.5(SiO4)4.5 host had a hexagonal crystal structure in the space group P63/m and unit cell parameters a = 9.418 Å, c = 6.900 Å. The as‐prepared phosphor showed a blue emission and all the main emission peaks were located at around 466 nm for different excitation wavelengths of 297, 333 and 391 nm. The temperature dependence of the photoluminescence property was investigated in the range 20–250 °C, and the emission intensity decreased to 71% of the initial value at room temperature on increasing the temperature to 150 °C. According to the classical theory of fluorescent thermal quenching, the activation energy (ΔE) for the thermal quenching luminescence of the as‐prepared Sr3.45Y6.5O2(PO4)1.5(SiO4)4.5:0.05Eu2+ phosphor was determined to be 0.20 eV. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
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New solid complex compounds of La(III), Ce(III), Pr(III), Nd(III), Sm(III), Eu(III) and Gd(III) ions with morin were synthesized. The molecular formula of the complexes is Ln(C15H9O7)3 · nH2O, where Ln is the cation of lanthanide and n = 6 for La(III), Sm(III), Gd(III) or n = 8 for Ce(III), Pr(III), Nd(III) and Eu(III). Thermogravimetric studies and the values of dehydration enthalpy indicate that water occurring in the compounds is not present in the inner coordination sphere of the complex. The structure of the complexes was determined on the basis of UV-visible, IR, MS, 1H NMR and 13C NMR analyses. It was found that in binding the lanthanide ions the following groups of morin take part: 3OH and 4CO in the case of complexes of La, Pr, Nd, Sm and Eu, or 5OH and 4CO in the case of complexes of Ce and Gd. The complexes are five- and six-membered chelate compounds. 相似文献
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Dong W. Choi Young S. Do Corbin J. Zea Marcus T. McEllistrem Sung-W. Lee Jeremy D. Semrau Nicola L. Pohl Clint J. Kisting Lori L. Scardino Scott C. Hartsel Eric S. Boyd Gill G. Geesey Theran P. Riedel Peter H. Shafe Kim A. Kranski John R. Tritsch William E. Antholine Alan A. DiSpirito 《Journal of inorganic biochemistry》2006,100(12):2150
Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ. 相似文献
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Nageswara Raju C Adinarayana Reddy C Sailaja S Seo HJ Sudhakar Reddy B 《Luminescence》2012,27(5):334-340
This article reports on the optical properties of Er3+ ions doped CdO–Bi2O3–B2O3 (CdBiB) glasses. The materials were characterized by optical absorption and emission spectra. By using Judd–Ofelt theory, the intensity parameters Ωλ (λ = 2, 4, 6) and also oscillatory strengths were calculated from the absorption spectra. The results were used to compute the radiative properties of Er3+:CdBiB glasses. The concentration quenching and energy transfer from Yb3+–Er3+ were explained. The stimulated emission cross‐section, full width at half maximum (FWHM) and FWHM × values are also calculated for all the Er3+:CdBiB glasses. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
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Masamitsu Doi Yoshinori Nishi Susumu Uchiyama Yuji Nishiuchi Hideki Nishio Takashi Nakazawa Tadayasu Ohkubo Yuji Kobayashi 《Journal of peptide science》2005,11(10):609-616
For the rational design of a stable collagen triple helix according to the conventional rule that the pyrrolidine puckerings of Pro, 4-hydroxyproline (Hyp) and 4-fluoroproline (fPro) should be down at the X-position and up at the Y-position in the X-Y-Gly repeated sequence for enhancing the triple helix propensities of collagen model peptides, a series of peptides were prepared in which X- and Y-positions were altogether occupied by Hyp(R), Hyp(S), fPro(R) or fPro(S). Contrary to our presumption that inducing the X-Y residues to adopt a down-up conformation would result in an increase in the thermal stability of peptides, the triple helices of (Hyp(S)-Hyp(R)-Gly)(10) and (fPro(S)-fPro(R)-Gly)(10) were less stable than those of (Pro-Hyp(R)-Gly)(10) and (Pro-fPro(R)-Gly)(10), respectively. As reported by B?chinger's and Zagari's groups, (Hyp(R)-Hyp(R)-Gly)(10) which could have an up-up conformation unfavorable for the triple helix, formed a triple helix that has a high thermal stability close to that of (Pro-Hyp(R)-Gly)(10). These results clearly show that the empirical rule based on the conformational preference of pyrrolidine ring at each of X and Y residues should not be regarded as still valid, at least for predicting the stability of collagen models in which both X and Y residues have electronegative groups at the 4-position. 相似文献
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