Cytology of infection of <Emphasis Type="Italic">Fusarium mangiferae</Emphasis> Britz in different malformed reproductive parts of mango

Aetiology of mango malformation (MM) has intrigued the scientists since its inception. The objective of the study was to glean an insight into association of the fungus, Fusarium mangiferae, with different malformed regions, viz. panicle-shoot juncture, apical buds, primary and secondary peduncles, in five exotic mango cultivars. Tissue assays revealed an infection of 88.5, 84.75 and 82.5% in cvs Zill, Sensation and Tommy Atkins, respectively. Least infection of 69.75% was found in cv. Keitt. No exotic cultivar was found to be free of fungal infection. Apical buds proved to be the potential infection site of the fungus amongst the four malformed regions, hosting maximum within-tissue infection of 86.2%. Determination of F. mangiferae at proximal and distant sites of the malformed panicles exhibited maximum recovery of 82.0% at 0 cm and only 3% at >30 cm distance beneath the panicle. In the case of non-malformed panicles, an infection of 14.0% was recorded at 0 cm distance while no detection could be made from non-malformed branches. Moreover, examination of ultra-thin bud sections under Transmission Electron Microscopy (TEM) revealed inter- and intra-cellular ramification of fungal hyphae, indicating fungal ingress in malformed bud tissues of local cv. Malda. The present studies explored the sites hosting the causal fungus in mango and provide convincing evidence that F. mangiferae is responsible for turning healthy tissues into the malformed condition. These findings suggest that inoculum specific management strategies are needed in future to curb malformation disease in mango orchards.     

Fusarium mangiferae localization in planta during initiation and development of mango malformation disease

Mango malformation disease (MMD), caused by Fusarium mangiferae, is a major constraint to mango production, causing significant yield reduction resulting in severe economic impact. The present study characterizes fungal localization in planta during initiation and development of vegetative and floral malformation. Young mango trees were artificially inoculated with a green fluorescent protein (GFP)‐expressing strain of F. mangiferae. Shoots and buds were sampled periodically over a period of more than a year and localization of the GFP‐expressing fungi was determined using confocal microscopy. Fungal localization appears to be epiphytic: mycelia remained in close contact with the plant surface but did not penetrate the tissue. In vegetative malformation and in young inflorescences, the fungus was confined to protected regions between scales, young leaf bases and buds. Fungal colonization was only very rarely detected on open leaves or on exposed shoot sections. In developed flowers, mycelia were localized mainly to protected regions at the base of the flower organs. Upon development of the inner flower organs, specific mycelial growth occurred around the anthers and the style. Mycelial penetration through the stylar tract into aborting carpels was observed. For several months, mycelia were confined to the surface of the organs and were not detected within plant tissues. Only at later stages, transient saprophytic growth of the fungus was detected causing the malformed inflorescences to senesce and collapse, concurrent with dispersion of conidia. Implications of the present study on MMD in natural field infections are discussed.     

云杉矮槲寄生的侵染对青杄光合与蒸腾作用的影响

 云杉矮槲寄生(Arceuthobium sichuanense)属半寄生性多年生种子植物,是青海省云杉天然林毁灭性生物灾害之一。本研究首次报道了云杉矮槲寄生在自然条件下可以侵染青杄,并对健康与染病青杄(Picea wilsonii)针叶形态及其光合日变化进行了测定。结果表明:1)染病青杄的针叶长度和宽度显著小于健康青杄(P＜0.001),而染病青杄的针叶比叶面积(SLA)显著大于健康青杄(P＜0.001);2)云杉矮槲寄生的侵染显著降低了青杄叶片的净光合速率、蒸腾速率以及气孔导度(P＜0.05),但不影响其胞间CO₂浓度(P =0.32);3)冗余分析(RDA)表明,云杉矮槲寄生的侵染导致青杄对不同环境因子的依赖程度发生变化,健康青杄表现为环境CO₂浓度(CO₂)＞空气温度(T_air)＞叶片温度(T_l)＞蒸汽压亏缺(Vpd)＞空气相对湿度(RH)＞光合有效辐射(PAR),而染病青杄则出现T_l＞RH＞T_air＞PAR＞Vpd＞CO₂,且T_l成为影响染病青杄叶片光合与蒸腾作用(P_n、T_r)的主要环境因子,且染病青杄对RH和PAR变化的响应更加敏感。此外,染病青杄叶片的水分利用率(WUE)显著低于健康寄主(P＜0.05)。因此,云杉矮槲寄生的侵染可降低青杄对环境的适应能力,从而加速寄主的衰老死亡。     

Integration of cultural and mechanical practices for management of the mango mealybug <Emphasis Type="Italic">Drosicha mangiferae</Emphasis>

Mango (Mangifera indica L.) is one of the most economically important trees which has been cultivated for several centuries. The tree is susceptible to insect damage and is attacked by leaf eaters, termites, root grubs, sapsuckers, gall formers, stem borers, pod borers and fruit borers. The mango mealybug Drosicha mangiferae Green (Hemiptera: Monophlebidae) is one of the most destructive pests in the Indo-Pak subcontinent, sometimes causing premature fruit drop. A combination of several management strategies such as use of entomopathogens, chemical insecticides and burning of adult females has been used to control D. mangiferae. Overreliance on insecticides has eliminated natural enemies, and we were therefore interested in investigating the impact of alternative insect pest management strategies such as cultural and mechanical techniques on D. mangiferae. The results of our studies suggested that different bands significantly stopped the upward movement of overwintering and surviving populations of D. mangiferae. To augment the bands’ results, mounding the tree with debris on a plastic sheet once a year was the most effective technique and resulted in maximum reduction of the nymphal population of D. mangiferae. The newly developed Haider band—designed in our laboratory in the present studies—was very successful in the field in controlling the upward movement of newly hatched nymphs on trees: only 0.8% of the nymphs crossed the band. Only 7% to 10% of the nymphs crossed plastic sheets, polyethylene sheets and funnel bands. The cotton and gunny bag (jute) bands were the least effective: 42% of the nymphs managed to cross them. The results suggested that employing cultural practices and bands together could reduce the need for insecticide treatments and offer a sustainable method for D. mangiferae control.     

植物内生枯草芽孢杆菌Em7菌株对葡萄灰霉病菌的抑菌活性

通过室内皿内对峙抑菌试验、分生孢子萌发抑制试验、离体果实接种试验以及电镜技术,研究测定了分离自小麦根部的植物内生枯草芽孢杆菌Em7菌液对葡萄灰霉病菌Botrytiscinerea Pers.的抑制作用及抑菌机理。结果表明:用Em7菌液处理葡萄灰霉病菌后,在PDA培养基上形成了明显的抑菌圈,直径达2.81 cm;菌液对分生孢子萌发的抑制率达到88.65%;经Em7菌液处理后,离体果实病情指数明显低于空白对照,相对防治效果达到78.92%。电镜观察发现,处理组菌丝生长异常,体表凹凸不平,局部膨大成结或缢缩,分枝变多,菌丝体内液泡增多,细胞壁增厚,细胞膜透性发生变化。表明植物内生枯草芽孢杆菌Em7菌株对葡萄灰霉病菌有良好的抑制作用,并且可以有效控制葡萄灰霉病的发生。     

马铃薯糖苷生物碱对枸杞镰孢菌果腐病的诱导抗性及相关防御酶活性的影响

为探索马铃薯糖苷生物碱诱导采后枸杞鲜果抗病性的效应,采用菌丝生长速率法测定了离体条件下马铃薯糖苷生物碱对枸杞鲜果采后主要致腐病原菌镰孢菌Fusarium sp.的抑菌活性;采用浸泡处理法测定了马铃薯糖苷生物碱对采后枸杞鲜果发病病情指数及对果实多酚氧化酶(PPO)、过氧化物酶(POD)、苯丙氨酸解氨酶(PAL)和超氧化物歧化酶(SOD)等相关防御酶活性的影响。结果表明:不同浓度马铃薯糖苷生物碱对镰孢菌均具有一定的抑制作用,EC50为0.11 g/mL;0.05～0.25 g/mL(提取原料)的马铃薯糖苷生物碱能显著降低采后枸杞鲜果病情指数,较对照降低了10.18%～38.51%;以0.15 g/mL(提取原料)的马铃薯糖苷生物碱处理后对枸杞鲜果抗果腐病的诱导效果最好,达45.81%;马铃薯糖苷生物碱处理枸杞鲜果后,果实中4种防御酶PPO、POD、PAL、SOD的活性均较对照有不同程度提高,分别于处理后第4、5、2、2天与对照差异达到最大,较对照提高了30.76%、21.34%、31.35%和21.91%。表明马铃薯糖苷生物碱能够诱导枸杞鲜果对采后病害的抗性效应,且采后抗病性可能与枸杞相关防御酶活性的增加有关。     

Transgenic indica rice expressing a bitter melon (Momordica charantia) class I chitinase gene (McCHIT1) confers enhanced resistance to Magnaporthe grisea and Rhizoctonia solani

McCHIT1 chitinase (DQ407723), a class I secretory endochitinase from bitter melon (Momordica charantia), had been demonstrated to enhance resistance against Phytophthora nicotianae and Verticillium wilt in transgenic tobacco and cotton. In order to obtain disease-resistant transgenic rice, McCHIT1 was transformed into a restorer line JinHui35 (Oryza sativa subsp. indica) by using the herbicide-resistance gene Bar as the selection marker. Transgenic rice lines and their progenies overexpressing the McCHIT1 gene showed enhanced resistance to Magnaporthe grisea (rice blast) and Rhizoctonia solani (sheath blight), two major fungal pathogens of rice. McCHIT1-transgenic rice confirmed the inheritance of the transgene and disease resistance to the subsequent generation. The T₂ transformants exhibited significantly increased tolerance to M. grisea, with a 30.0 to 85.7 reduction in disease index, and R. solani, with a 25.0 to 43.0 reduction in disease index, based on that of the control as 100. These results indicated that over-expression of the McCHIT1 gene could lead to partial disease reduction against these two important pathogens in transgenic rice.     

香蕉花蕾注射螺虫乙酯和吡虫啉对黄胸蓟马的防效及药剂在果实中的残留

黄胸蓟马是中国香蕉上重要害虫,生产上对该虫仍缺乏较为有效的防治手段。本研究采用香蕉花蕾注射法施用22.4%螺虫乙酯悬浮剂 (SC) 和70%吡虫啉水分散粒剂 (WG),研究了其对黄胸蓟马的防效,并采用超高效液相色谱-串联质谱法 (UPLC-MS/MS) 分析了药剂在香蕉果实中的残留。药效试验表明:于香蕉现蕾初期,22.4%螺虫乙酯SC和70%吡虫啉WG分别按有效成分0.12和0.18 g/株的剂量注射施药1次,对黄胸蓟马的防效分别为89%和86%。残留试验表明:花蕾注射施药后,螺虫乙酯和吡虫啉在香蕉果实中的半衰期分别为9.2和6.5 d,且在施药后95 d的香蕉成熟果实中未检测到其残留。本研究表明,香蕉花蕾注射螺虫乙酯与吡虫啉对黄胸蓟马具有良好的防治效果与安全性,可推荐在香蕉园轮换使用。     

水稻抗白叶枯病基因Xa47(t) a的敲除及抗性鉴定

为鉴定水稻Xa47(t)a基因对白叶枯病的抗性,以水稻种质L214为材料,通过构建针对Xa47(t)a基因的Xa47(t)a-Cas9敲除载体来获得敲除突变体,利用生物信息学技术对突变的Xa47(t)a基因进行突变类型分析,同时采用实时荧光定量PCR(quantitative real-time PCR,qPCR)技术分析突变体中Xa47(t)a及病程相关基因的表达情况,并于水稻孕穗期对突变体及其野生型植株接种11株白叶枯病菌Xanthomonas oryzae pv. oryzae菌株进行抗性鉴定。结果表明,在Xa47(t)a基因的第2外显子区域进行基因编辑后成功获得25株T₀代突变体株系;测序分析发现T₀代突变体株系中有13种不同的突变体类型,其中纯合突变体有3种类型,且突变位点均在靶标位点的11位碱基处缺失1～4个A碱基;氨基酸序列分析发现大部分突变体中Xa47a编码的蛋白翻译会提前终止,由原来的803个氨基酸变为144～166个氨基酸;qPCR分析结果表明突变体中Xa47(t)a及大部分病程相关基因的表达水平显著低于野生型株系;抗性鉴...     

低温胁迫下转ICE1基因水稻养分变化的研究

采用盆栽试验,选用转ICE1基因水稻T_4-8株系和T_4-9株系及未转基因水稻（Oryza sativa L.）品种垦鉴稻10号为试验材料,研究苗期低温胁迫对转基因水稻氮、磷、钾养分吸收的影响。结果表明,低温胁迫期间,转基因水稻幼苗丙二醛含量维持在较低水平,SOD活性维持在较高水平;地上部分氮、磷、钾含量变化不大,一直维持在较高水平;地下部分氮、磷、钾含量呈缓慢下降趋势,但降幅比非转基因水稻小,在胁迫第10天,T_4-8株系和T_4-9株系氮含量均高出对照13.86%,磷含量分别高出42.31%和50.00%,钾含量均高出85.71%。说明在低温胁迫条件下,ICE1基因过量表达可以增强水稻的抗寒性,减轻低温对水稻的伤害,保持根系较强的吸收养分能力。     

酵母pac1基因介导对葡萄B病毒的抗性

为明确广谱性抗病毒基因—酵母pac1基因对葡萄B病毒(Grapevine virus B,GVB)的抗性效果,通过农杆菌介导的遗传转化,将pac1基因导入西方烟37B,对转基因植株进行PCR鉴定及Southern blot分析,通过病毒摩擦接种观察症状以及实时荧光定量RT-PCR检测植株体内病毒含量,并对转基因植株抗病性进行初步鉴定。结果表明,目的基因pac1成功导入并整合至西方烟37B基因组,共获得10个转基因株系。不同株系的T1代烟草中阳性植株比例为16.7%~72.7%,表明目的基因可成功遗传到子代。接种病毒后转基因植株普遍延迟发病,但后期症状与非转基因对照相似,其中仅1个转基因株系B6具有不表现典型症状等抗性反应。接种植株病毒含量检测中,所有转基因植株均检测到病毒存在,但表现为抗病的B6株系中病毒含量显著低于非转基因对照,表明该转基因植株虽不能完全抵抗GVB侵染,但对GVB具有耐病性。     

Characterization of Fusarium mangiferae isolates from mango malformation disease in Southern Spain

During the last years, Fusarium strains have been isolated from shoots and inflorescences of mango trees affected with floral and vegetative malformation in different orchards from the Axarquía region (south of Spain), highlighting the identification of Fusarium mangiferae. With the aim of elucidate epidemiological aspects and design more efficient control strategies, population diversity among the strains of F. mangiferae associated with MMD in Spain was determined by ap-PCR, RAPD-PCR, vegetative compatibility groups (VCGs) and mating type analyses. Three different VCGs were found among the Fusarium mangiferae Spanish isolates, two of them showing similar ap–PCR and RAPD profiles. PCR with primers specific for the mating type (MAT) alleles resulted in amplification of the MAT-2 allele fragment among the majority of the isolates, there being only two isolates MAT-1. This population diversity suggests at least three possible independent introductions of the pathogen into the Axarquía region.     

Fusarium solani endo-polygalacturonase from decayed muskmelon fruit: purification and characterization

Fusarium solani is one of the more important fungal pathogens involved in pre- and post-harvest decay of muskmelon fruit. Production of polygalacturonase (PG), by F. solani was studied in vitro and in vivo . The fungus produced at least 14 PG isozymes with pIs of 4.5 to 9.5 in shake culture using pectin as the sole carbon source. When glucose and pectin were used in combination as the carbon source, total PG activity decreased substantially as compared to pectin alone, suggesting that glucose may suppress PG production in vitro . Only one PG isozyme, designated as PG1, was detected in extracts from infected fruit tissue. PG1 from decayed fruit was purified to homogeneity by protein extraction, ultrafiltration, gel filtration chromatography, and cation exchange chromatography. The molecular weight of PG1 was estimated at 38 kDa based on SDS-PAGE with a pI of 9.5 according to IEF-PAGE. PG1 exhibited only endo-PG activity based on viscosity reduction and thin layer chromatography analysis of products released by enzymatic action. The optimum pH for PG1 activity was 6. TheK_m and V_maxof PG1 using polygalacturonic acid as the substrate were 1.34 mg ml^-1and 0.30 unit μg protein^-1, respectively. PG1 effectively macerated fruit tissue which suggests that it may play an important role in decay of muskmelon fruit caused by F. solani .     

不同改良剂配施对河套灌区碱化土壤理化性质及枸杞生长的影响

为了评价脱硫石膏配施不同功能改良剂对宁夏河套灌区碱化土壤改良效果，进而筛选出适合河套地区碱化土壤改良的最佳方案，本研究以枸杞(Lycium chinense)为供试材料，在宁夏河套灌区设立碱化土壤改良田间试验，设对照(T₁)、单施脱硫石膏(T₂)、脱硫石膏+醋糟+菌肥(T₃)、脱硫石膏+菌肥(T₄)、脱硫石膏+醋糟+菌肥+保水剂(T₅)、脱硫石膏+微肥(T₆)、脱硫石膏+诱抗素(T₇)7个处理，于2013—2016年连续开展田间试验对比分析不同改良措施对土壤盐碱指标、养分状况以及枸杞农艺性状(成活率/保存率、株高和产量)的影响。结果表明：改良4年间T₂～T₇处理在提高0～20 cm土层土壤有机碳(5.4%～88.8%)、全氮(8.0%～31.3%)、碱解氮(11.4%～41.7%),降低pH值(4.8%～10.3%),钠吸附性比SAR(5.5%～51.6%)和全盐含量(5.5%～51.6%)...     

Morphology,phylogeny, and pathogenicity of Trichothecium,Alternaria, and Fusarium species associated with panicle rot on Chenopodium quinoa in Shanxi Province,China

Quinoa panicle rot (QPR) is a novel disease that poses a significant threat to quinoa production in China. Typical symptoms on panicles include a film of pale pink, grey-white, or dark brown mould on the grains during the grain-filling stage. Furthermore, QPR causes quinoa grain discolouration, unfilling, and malformation. In total, 37 isolates were identified as belonging to three species: Trichothecium roseum (nine isolates), Alternaria alternata (12), and Fusarium citri (16) based on morphology, and phylogenetic and pathogenicity characterization. The present study shows for the first time that T. roseum, A. alternata, and F. citri are the pathogens responsible for QPR. An evaluation of the growth and germination rates revealed a significant difference among the three species, with T. roseum and F. citri isolates having higher fitness in warmer (25–30℃) and humid conditions (water activity ≥0.98). However, A. alternata preferred cooler (20–25℃) and more arid conditions, and germinated in a wide range of water activities (water activity of 0.90–1.00). Among the three species, T. roseum and F. citri are probably responsible for the pink and grey diseased grains in humid regions, and A. alternata for the black-brown diseased grains in arid regions. Pathogenicity tests showed that all three species could infect the quinoa panicles. The results of this study provide a basis for the recognition and management of QPR.     

解淀粉芽胞杆菌菌株HRH317对感染串珠镰孢菌玉米幼苗伏马毒素B1含量及相关防御酶活性的影响

为探讨解淀粉芽胞杆菌Bacillus amyloliquefaciens菌株HRH317对感染串珠镰孢菌Fusarium moniliforme玉米幼苗产生伏马毒素B_1(FB_1)的影响,采用牛津杯法测定菌株HRH317对串珠镰孢菌的抑制活性,并通过浸种处理进行盆栽试验,应用高效液相色谱技术对生长至3叶期后不同时间玉米幼苗叶片中FB_1含量进行测定,同时于室内测定玉米幼苗叶片防御酶超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、苯丙氨酸解氨酶(PAL)和过氧化物酶(POD)的活性。结果表明:解淀粉芽胞杆菌菌株HRH317能明显抑制串珠镰孢菌生长,抑菌圈直径平均可达33.31 mm;玉米幼苗生长至3叶期后1～6 d,菌株HRH317能有效抑制玉米植株体内FB_1含量,经串珠镰孢菌分生孢子悬浮液与菌株HRH317菌悬液1∶1混合液处理玉米种子后,对幼苗中FB_1的抑制率为59.20%～75.70%;而玉米种子先接种菌株HRH317菌悬液后接种串珠镰孢菌分生孢子悬浮液处理对幼苗中FB_1的抑制率为76.77%～88.10%。且这2种处理中幼苗叶片的SOD、CAT、PAL和POD活性均较对照有不同程度提高,其峰值是对照的1.24～5.45倍。表明解淀粉芽胞杆菌菌株HRH317可通过抑制FB_1产生来降低串珠镰孢菌对玉米幼苗的侵害,同时能诱导玉米植株体内防御酶活性的表达而增强其系统抗性,在防治玉米穗腐病方面具有潜在的应用价值。     

短翅蚜小蜂对桃蚜的取食和寄生功能反应

为评估短翅蚜小蜂对桃蚜的搜寻及控害潜能,采用叶碟法研究了短翅蚜小蜂对甘蓝和辣椒2种植物上桃蚜2龄若虫的取食与寄生行为。结果表明,短翅蚜小蜂对甘蓝桃蚜和辣椒桃蚜的取食和寄生功能反应均符合Holling II及Holling III型方程。短翅蚜小蜂的取食和寄生搜寻效应均随蚜虫密度的增加而降低,当桃蚜密度小于35头时,短翅蚜小蜂对甘蓝桃蚜的取食搜寻效应大于辣椒桃蚜,而当桃蚜密度大于35头时,短翅蚜小蜂对辣椒桃蚜的取食搜寻效应大于甘蓝桃蚜;短翅蚜小蜂在所有密度下对辣椒桃蚜的寄生搜寻效应均大于甘蓝桃蚜。短翅蚜小蜂取食甘蓝桃蚜的瞬间攻击率a'为0.3289,处理时间T_h为0.2597,均大于辣椒桃蚜,寄生甘蓝桃蚜的瞬时攻击率a'为0.8213,小于辣椒桃蚜,而处理时间T_h为0.0275,大于寄生辣椒桃蚜;短翅蚜小蜂对甘蓝桃蚜的理论最大取食量和寄生量均小于辣椒桃蚜。研究表明,短翅蚜小蜂对不同密度的桃蚜均有一定的控制能力,且对辣椒桃蚜的控制作用大于甘蓝桃蚜。     

Harpin-elicited hypersensitive cell death and pathogen resistance require the NDR1 and EDS1 genes

Plants sprayed with harpin, a bacterial protein that induces hypersensitive cell death (HCD), develop systemic acquired resistance (SAR) without macroscopic necrosis. HCD sometimes accompanies the development of resistance conferred by resistance (R) genes. In Arabidopsis, some R genes require one or both of the signalling components NDR1 and EDS1 for function. This study addresses whether HCD, NDR1 and EDS1 are required for induction of SAR by harpin. When Arabidopsis and tobacco leaves were sprayed with harpin, microscopic hypersensitive response (micro-HR) lesions developed. Systemic expression of PR genes and the development of resistance were accompanied by micro-HR, except in the ndr1-1 mutant, in which harpin induced micro-HR without the development of resistance or expression of the PR-1 gene. Cell death and resistance did not occur following treatment with harpin in plants that could not accumulate salicylic acid. Harpin also failed to induce resistance in Arabidopsis eds1-1 mutants. Therefore, harpin-induced resistance seems to develop concomitantly with cell death and resistance requires NDR1 and EDS1.     

兰州百合不同连作年限土壤中化感物质的检测及其自毒效应的研究

为探讨兰州百合(Lilium davidii var.unicolor)连作障碍的可能机理,收集了兰州百合正茬、连作2 a及连作4 a不同生育期的根际土壤,采用GC-MS技术对不同土壤中的化感物质进行了鉴定,并通过生物试验验证了典型自毒物质对苯二甲酸二辛酯(D)和抗氧剂2246(A)对兰州百合幼苗生长的影响。结果显示:从生长旺盛期兰州百合正茬、连作2 a及4 a土壤中分别鉴定出11、15和19种化合物,收获期鉴定出9、15及17种成分,主要包括:醇类、醛类、酯类、酚酸类及少量萜类化合物。其中,对苯二甲酸二辛酯(D)在不同生育期连作土壤中均存在,抗氧剂2246(A)除收获期正茬土壤外在其余土壤中也均存在,且二者相对含量均较高。生物试验结果表明,0.2 mg·mL~(-1)时,D_(0.2)对兰州百合幼苗生长的综合化感效应(SE)为-0.003,具有抑制效应,A_(0.2)的SE值为0.131,具有促进作用;5.0 mg·mL~(-1)浓度下,D_5和A_5均能抑制兰州百合幼苗的生长,SE值分别为-0.489和-0.040,对苯二甲酸二辛酯的抑制效应更强;共施条件下,D_(0.2)A_5和D_5A_5混合液仍能抑制兰州百合幼苗生长,但未体现出2种成分单施时的抑制协同效应;D_5A_(0.2)混合液表现出抑制作用,D_(0.2)A_(0.2)表现出促进作用,体现了2种成分单施时相反作用的叠加效应。