糜子的小孢子发生与花粉发育

观察结果表明,糜子小孢子发生与花粉发育的细胞学过程,与稻麦等禾本科作物相似:减数分裂属顺序型,一般形成等面形四分体;也观察到线形、T形及各种倾斜形的四分体;小孢子经两次有丝分裂发育成三核型花粉粒;成熟的花粉粒为球形,具一个萌发孔,直径48(45～52)μm.花粉发育过程中,生殖细胞的运动、淀粉积累时期及花粉粒体积增大动态的观察结果与一些报道不同.糜子的小孢子发生和花粉发育与花药长度存在密切关系,而花药长度随时间呈S形增长方式.本文利用上述关系求得小孢子发生与花粉发育各阶段的经历时间.     

基于方向一致性特征的小麦条锈病与白粉病识别方法

针对小麦条锈病、白粉病这2种病斑颜色特征相近、形状特征不明显,但在方向分布的一致性上却存在较大差别这一特点,提出了一种方向一致性描述方法。通过不同的方向核与图像卷积得到多个方向图和边缘,对每个方向图依据边缘图进行统计得到图像的方向分布直方图;并计算方向分布直方图的标准差,作为图像方向分布的一致性特征。该方法能够较好地抑制噪声影响,得到的结果符合图像的实际分布情况。利用该方法对小麦病斑进行特征提取,并应用于小麦条锈病与白粉病的病斑识别实验中。实验结果表明,所提出的方向一致性特征使条锈病与白粉病的区别度较大,准确识别率达到99%。     

冬枣锈病发生与叶龄及其解剖结构关系的研究

为探讨冬枣叶龄、叶片解剖结构与锈病侵染和发病程度的关系，对冬枣3种不同叶龄的叶片进行锈病接种试验，并对叶片组织解剖结构进行了测定。结果表明：3种叶龄叶片感病程度由低到高依次为：成熟叶< 长成叶<嫩叶，由此可见，成熟叶对锈病的抵抗力最强；3种叶龄叶解剖性状在角质层厚度、上表皮厚度、下表皮厚度、叶片厚度、栅栏组织厚度、海绵组织厚度、栅海比、叶片结构紧密度、叶片结构疏松度、气孔密度和气孔大小等指标有显著差异，但气孔开张结构性状差异不显著。文章筛选出了与冬枣锈病发生有关的叶片形态结构指标，为合理的控制冬枣锈病和筛选抗锈病冬枣优良单株的提供了理论依据。     

谷子株高及穗部性状主基因+多基因混合遗传模型分析

【目的】株高和穗部性状是影响谷子产量的关键性状。探究谷子株高及穗部性状表型变异的遗传规律,为相关性状的遗传改良与基因定位提供参考依据。【方法】以谷子优质品种豫谷18为共同父本,分别与黄软谷和红酒谷杂交,构建2个分别包含250个家系的重组自交系F₇群体（YYRIL和YRRIL）。采用主基因+多基因混合遗传模型,对YYRIL和YRRIL群体在2个环境下的株高、穗长、穗下节间长、穗码数、穗粒重等5个农艺性状的表型数据进行遗传分析。【结果】5个性状在所有环境中均表现连续变异且存在超亲分离现象,峰度和偏度绝对值小于1,近似正态分布,呈现数量性状的典型遗传特点。性状间相关性分析表明株高与穗长、穗下节间长在所有环境中均呈极显著正相关,穗码数与穗粒重呈极显著正相关。遗传模型分析显示YYRIL和YRRIL群体株高的最适遗传模型分别为PG-AI和PG-A多基因模型,多基因遗传率分别为95.15%和91.27%。2个群体穗码数的最适模型均为PG-AI,多基因遗传率为70.07%—71.58%。穗下节间长在2个群体的最适遗传模型分别为4MG-CEA和3MG-CEA,均为等加性主基因模型。穗下节间长在YYRIL群体的主基因遗传率为9.69%,4对主基因加性效应值相等,均为-0.34,具有负向效应;穗下节间长在YRRIL群体的主基因遗传率为45.78%,3对主基因加性效应值相等,均为1.17,具有正向效应。穗长在YYRIL群体的最适模型为MX2-ED-A,即2对显性上位主基因+加性多基因模型,主基因遗传率为43.56%,多基因遗传率为50.56%。控制穗长的2对主基因加性效应值分别为-1.21、1.68,多基因加性效应较小,为-0.0017;穗长在YRRIL群体的最适模型为MX2-AE-A,即2对累加作用主基因,加性多基因混合遗传模型;穗长的主基因遗传率为46.40%,多基因遗传率为46.91%。控制穗长的第1对主基因加性效应值为1.53,具有正向效应,第1对主基因加性×第2对主基因加性上位性互作效应值是0.60,多基因加性效应值为-0.47,表现为较低的负向遗传效应。穗粒重在YYRIL群体的最适遗传模型为MX2-ED-A;符合2对显性上位主基因+加性多基因模型,主基因遗传率为69.09%,多基因遗传率为12.08%;控制穗粒重的2对主基因加性效应值分别为0.58、5.82,以第2对主基因的加性效应为主,多基因加性效应值为-3.81。穗粒重在YRRIL群体的最适遗传模型为3MG-PEA,即3对部分等加性主基因遗传模型;穗粒重的主基因遗传率为81.10%,3对主基因加性效应值分别为-2.68、-2.68和2.66,前2对主基因的加性效应值相同,且均为负向效应。【结论】谷子株高、穗码数的最适遗传模型相似,均服从多基因遗传,遗传率较高,受环境影响较小;穗下节间长的遗传受主基因控制,主基因遗传率偏低,受环境影响较大,在栽培中应充分考虑环境因素;穗长遗传受主基因和多基因共同控制;穗粒重在2个群体均服从主基因遗传,主基因遗传率较高,可能存在主效QTL。     

竹秆锈病防治试验及其推广应用

经多年调查，浙江省是竹秆锈病严重常发区，被害种竹已达１７个以上，其中对早竹的危害十分突出，该病已成为竹子发展的一个限制性因子之一。经不同方法的对比试验，表明刮涂法和刮涂后涂药防治效果达８８．９％以上，效果十分显著。在德清推广防治技术后，基本控制病情，并取得十分显著的经济、生态社会效益。     

An advisory model for control of Puccinia recondita in winter wheat

Epidemics ofPuccinia recondita and resulting yield loss of winter wheat were studied in field experiments over three seasons in the Netherlands. Results are reported and used to construct an advisory model for control of brown rust, based on rust monitoring. If the fraction of leaves with rust (I) at a certain development stage is determined, the average number of rust sori per leaf (M) was estimated by: M=EXP(1.84+1.39ln(ln[1/(1-I)]). The final number of sori per leaf (Mf) at early dough was forecast by an exponential growth: Mf=M·EXP(RGR·t). The relative growth rate (RGR) averaged 0.163/day and the forecasting period, t, until early dough, was derived from published data. The forecast number of sori-days per leaf (S, AUDPC-value) was then obtained by: S=(Mf-M)/RGR. Yield loss (kg/ha) by brown rust was 1.15 times the number of sori-days per leaf at low rust intensities. The efficacy of the fungicides used was 85%. The forecast avoidable yield loss (L, kg/ha) was calculated by: L=0.85 (1.15 S). Economic thresholds for brown rust control at different development stages are given for Dutch wheat fields at a cost level of 270 kg/ha for one fungicide application.     

Postponed germination of Puccinia recondita urediospores deposited on wheat seedlings. II. Infectivity of urediospores after postponed germination

Urediospores ofPuccinia recondita f.sp.tritici were applied to wheat seedlings. Inoculated plants were placed in a growth chamber to expose the spores to dry periods from zero to nine days at near-optimal temperatures (ca 18 °C). The dry period was followed by a wet period varying from 2 to 24 hours for germination of spores and infection of plants. Infection results were subjected to analysis of variance. The main effects dry period, wet period, and temperature were highly significant. The dry period×wet period interaction was significant. The interaction implied that the effects of post-detachment, ripening of germinable spores appeared in their resulting infectivity. There were two forms of post-detachment ripening, a slow ripening during the dry period and a faster ripening during the wet period. The two forms of ripening showed a non-additive compensatory interaction. The effect of post-detachment ripening on infectivity of germinated spores was more pronounced at 15 than, at 18 or 20 °C; the effect was strongest during the first day of the dry period. At dry periods of over 6 days, infectivity of germinated spores decreased, especially at the higher temperatures. Prolonged exposure, of spores to a dry period apparently damages the spores even though they are still able to germinate.Samenvatting Uredosporen van de bruine roest van tarwe (Puccinia recondita f.sp.tritici) werden over het eerste blad van tarwekiemplanten verstoven. De aldus geïnoculeerde planten werden in een klimaatkamer geplaatst bij ca. 18 °C om de sporen bloot te stellen aan droge perioden van 0 tot 9 dagen. De droge perioden werden gevolgd door natte perioden van 2 tot 24 uur om de sporen te laten kiemen en de planten te infecteren. Na de natte periode werden de planten bij verschillende temperature geplaatst om de latente periode en de vorming van sporenhoopjes te bepalen. De hoofdeffecten op de vorming van sporenhoopjes waren zeer significant: duur van de droge periode, duur van de natte periode en temperatuur. Twee vormen van sporenrijping werden gevonden bij rijping vnn sporen, die los op het blad lagen (rijping, buiten de sporenhoopjes), een langzame rijping tijdens de droge periode en een snelle rijping tijdens de natte periode. Deze twee vormen van rijping vertoonden statistische interactie met enige wederzijdse compensatie. Het effect van deze sporenrijping (buiten de sporenhoopjes) op de infectiviteit van gekiemde sporen was bij 15 °C duidelijker dan bij 18 en 20 °C; het effect was het sterkst tijdens de eerste dag van de droge periode. Bij droge periodes langer dan 6 dagen daalde de infectiviteit, vooral bij de hogere temperaturen.     

丰抗2号冬小麦抗锈性基因的染色体定位研究

 用"中国春"单体系和抗锈品种"丰抗2号"杂交,对其抗病基因进行染色体定位。结果表明,丰抗2号对条锈菌小种25号的单显性抗病基因位于5B染色体上;对叶锈菌小种38号的单显性抗病基因位于5A染色体上。位于5B和5A染色体上的两个分别抵抗条锈和叶锈病的基因可能是新的抗病基因。     

梨胶锈菌的重寄生菌研究——Ⅱ重寄生菌的生物学特性

 梨胶锈菌(Cymnosporangium asiaticum Miyabe ex Yamada)的重寄生菌(Tuberculina vinosa Sacc.)在PDA、综合马铃薯和梨叶汁培养基上能生长、产孢,以PDA最好,Czapek和硝酸铵蔗糖上生长差且不产孢。菌丝生长和产孢的适温20~30℃,适宜pH6~9,荧光可促进产孢而黑光有抑制作用。对碳源的利用,菌丝生长和干重以甘露醇、葡萄糖等6种碳源为好,甘露醇最佳,淀粉最差;葡萄糖、蔗糖、果糖和甘露醇中均能产孢,以葡萄糖最好。对氮源的利用,菌丝生长及干重以硝酸钾、甘氨酸和蛋白胨为好;产孢以天冬酰胺、蛋白胨和硝酸钾为好,甘氨酸和谷氨酸不产孢。孢子萌发适温15~30℃,相对湿度65~100%均能萌发,在水滴中萌发率最高,低于50%不萌发;最适pH4~6,低于pH3和高于pH8不萌发;光照有利于孢子萌发。     

Competition and interactions among stripe rust pathotypes in wheat-cultivar mixtures

A series of experiments was conducted with wheat stripe rust to analyse competition between simple and complex pathotypes in host mixtures. Two different pathotype combinations were tested, with different host components. Each combination included a complex (able to infect two host components) and two simple pathotypes. For one of the combinations, induced resistance was tested in a separate experiment as a possible interaction among pathotypes. Disease severity and pathotype frequencies were measured three times during the epidemic, on each host component grown in pure stands and in mixtures. In one of the experiments, pathotype frequencies were also measured within secondary foci. One of the complex pathotypes appeared to have a low fitness on one of the host components and did not significantly increase in frequency in host mixtures relative to pure stands. The average frequency of the other complex pathotype increased during the first epidemic cycles, but remained stable afterwards, below expected values. The results suggest that the development of complex pathotypes in host mixtures may be influenced by differential aggressiveness on the host components, by induced resistance and by random effects resulting from the formation of disease foci, and depends on pathogen autoinfection rate and dispersal mechanisms.