生姜癞皮病的发生危害及病原初步鉴定

生姜癞皮病在山东7月开始发病,8月中旬至9月中旬为盛发期。病株植株矮小、茎细、分枝少,叶色变淡,根茎表皮疣裂,根系腐烂,产量品质降低。病原物为南方根结线虫。砂质土壤、连作重茬、过量施钾肥均可加重该病的发生。     

A modified fluorometric method to quantify the concentration effect (pI50) of photosystem II-inhibiting herbicides

Chlorophyll fluorescence induction curves of isolated thylakoids were measured in the absence and in the presence of various concentrations of photosystem II-inhibiting herbicides. A mathematical program was applied to simulate the curves. Based on these simulated curves a new method is developed to determine the concentration effect (pI₅₀) of the herbicides. The results of the new method correspond well with reported values in the literature. The method is very convenient and time-saving.     

The potential for the Rapid Screening of Potato Cultivars (Solanum tuberosum) for Resistance to Powdery Scab (Spongospora subterranea) using a Laboratory Bioassay

Powdery scab of potato, once established in a field, is difficult to control because of the longevity of the resting spores (cystosori) of the causal organism, Spongospora subterranea f.sp. subterranea. Host resistance is likely to be the most efficient in a long-term control strategy for preventing build-up of field inoculum and spread of the disease. Resistance screening of potato cultivars is mostly done in laborious field trials where disease development is likely to be unpredictable. A bioassay with potato tissue cultured plantlets and cystosori as inoculum is described and was tested for its potential to screen potato cultivars at an early stage for their relative susceptibility to powdery scab by comparing the lab results with field data. With cystosori inoculum of Swiss origin, the laboratory test showed clear differences between the potato cultivars in the severity of zoosporangial root infection which correlated better with ranked tuber infection data, compared to root galling. There are apparent differences in the relative trends in susceptibility between roots and tubers of five selected cultivars when using naturally infested soil instead of prepared cystosori as inoculum in the lab bioassay. Furthermore, differences in the severity of zoosporangial root infection of two selected cultivars were found when cystosori from different countries where used as inoculum. A possible host genotype × pathogen interaction is discussed. The bioassay has the potential to screen and select for resistant material at an early breeding stage thus making field trials not unnecessary but more economical. It will allow the use of a standard set of pathogen collections and facilitate testing for inoculum virulence in infested soils.     

植物化感作用影响因素的再认识

土壤养分、酶、微生物、本底特性,根茬还田、水分、植物根系、种植体系和种植模式与化感作用的互作关系,表明这些因子可通过对土壤养分有效性、微生物种群结构、土壤酶活性和化感物质浓度的影响而对化感作用产生直接或间接影响,这些可为通过化感作用途径构建高效农田生态系统提供新的思路.     

四个紫花苜蓿品种种子萌发期耐盐性研究

在实验室内模拟的盐分条件下,用不同浓度的Na Cl盐溶液对4个紫花苜蓿品种(中苜1号、中苜3号、中草3号和陇东苜蓿)种子萌发期进行盐胁迫处理。结果表明:低浓度(0.2%和0.4%)的盐溶液对苜蓿的发芽率和幼苗苗高抑制作用不显著,对幼根具有一定的刺激作用。0.8%和1.0%的Na Cl溶液处理下发芽率、0.6%的Na Cl溶液处理下的幼苗苗高和幼根生长量可以作为苜蓿种子萌发期耐盐性鉴定指标。对四个紫花苜蓿品种的发芽率、幼苗苗高、幼根生长量、耐盐半致死浓度四个指标进行综合分析,结果表明:中苜1号耐盐性最强,其次是中苜3号和中草3号,陇东苜蓿最弱。     

盐胁迫对菘蓝幼苗生长和抗性生理的影响

以“定蓝1号”为试验材料,采用不同浓度NaCl溶液(0,30,60,90,120和150 mmol·L^-1)对菘蓝幼苗进行处理,胁迫14 d后测定了其生长指标、生物量积累、叶片相对含水量、根系活力、根质膜透性、渗透调节物质含量以及抗氧化酶活性等指标,分析不同程度盐胁迫对菘蓝幼苗生长和抗性生理的影响。结果表明:NaCl胁迫对菘蓝幼苗株高和根长都有抑制作用,对根和叶的物质积累也有显著影响,并随浓度的递增呈降低的趋势;菘蓝幼苗叶片相对含水量和根系活力均随NaCl浓度的增加呈现下降趋势,而根质膜透性、叶片脯氨酸含量则呈升高趋势;丙二醛(MDA)含量、组织自动氧化速率(RAD)、过氧化物酶(POD)活性和超氧化物歧化酶(SOD)活性都随NaCl浓度的增加呈先升高后降低的趋势。但当NaCl浓度低于90 mmol·L^-1时,菘蓝幼苗的生长没有受到盐胁迫的明显抑制,根系活力降低不明显,脯氨酸、丙二醛含量和保护酶活性也未显著升高,说明菘蓝幼苗对低浓度盐环境具有一定的耐受性。     

紫花苜蓿形态和生理指标响应干旱胁迫的品种特异性

为研究紫花苜蓿在叶片和根系水平上响应干旱胁迫的形态和生理的品种特异性规律,在温室内分析了干旱胁迫下WL363HQ和巨能7紫花苜蓿株高、分枝数、生物量及叶片和根系中丙二醛(MDA)、脯氨酸、抗氧化酶类物质、C、N含量、C/N、稳定性C同位素(δ13C)和稳定性N同位素(δ15N).结果表明:干旱胁迫显著降低了供试品种地上...     

小麦茎基腐病抗性QTL的分析

为挖掘更多的茎基腐病抗性QTL用于分子标记辅助育种,以中抗茎基腐病品种CI12633和感茎基腐病品种扬麦158的重组自交系群体为材料,采用SSR和SNP等分子标记对群体中的94个家系进行基因型分析,绘制遗传连锁图,并结合3次室内群体的茎基腐病抗性鉴定结果对小麦茎基腐病抗性QTL进行定位.结果表明,与小麦茎基腐病抗性相关...     

利用生物反应器大量生产人参不定根

在5 L气球型生物反应器中,采用完全浸没式培养方式,人参不定根鲜重和干重明显优于间歇浸没式培养;在培养开始时一次性注入含50 g/L蔗糖的培养基,可促进人参不定根鲜重和干重的增加;接种时,将不定根切成1 cm长、接种量为20 g时接种较适宜;增殖培养周期以30天为宜.