Colonization and histopathology of susceptible and resistant carnation cultivars infected with Fusarium oxysporum f. sp. dianthi

Stems of the susceptible Early Sam and resistant Novada carnations were inoculated with a conidial suspension ofFusarium oxysporum f. sp.dianthi. Stem segments of either cultivar were sampled regularly and used for determination of fungal growth and for microscopical investigation.Early Sam showed typicalFusarium wilt symptoms and its stems were colonized intensively. The observed vascular browning appeared to be caused by discolouration of primary walls of infected vessels and surrounding cells. Vessels were rarely occluded with gel. Cell wall degradation led to the formation of stem cavities. Hyperplasia of xylem parenchyma was not seen.In Novada, fungal colonization remained low throughout the experiment. Macroscopic symptoms were absent except for longitudinal bursts in the stem, which appeared to be caused by hyperplasia of xylem parenchyma bordering infection. Vascular gelation occurred in the infected tissues, causing some vascular browning also. Xylem vessel regeneration was observed in the hyperplastic layer. Cavities were not formed, and wall discolouration was rare. Vascular gelation is considered part of theFusarium wilt resistance mechanism. It is followed by xylem vessel regeneration, which expresses a general plant response to vascular dysfunction rather than being part of the resistance mechanism.Although of different origin, vascular browning as such occurs in both susceptible and resistant interactions. In breeding for resistance, care should hence be taken with the current use of browning as an indication of disease.Samenvatting Anjers van de vatbare cultivar Early Sam en de resistente cultivar Novada werden geïnoculeerd met een conidiënsuspensie vanFusarium oxysporum f. sp.dianthi. Van beide cultivars werden regelmatig stengeldelen geoogst om deze microscopisch te onderzoeken en om de schimmelgroei te bepalen.Early Sam vertoonde de voor deze verwelkingsziekte kenmerkende symptomen en werd intensief gekoloniseerd. Aan het vaatweefsel waargenomen bruinkleuring bleek veroorzaakt te worden door verkleuring van de primaire wanden van geïnfecteerde vaten en de hen omringende cellen. Zelden trad er in de vaten gomvorming op. Celwandafbraak veroorzaakte de vorming van holten in de stengel. Hyperplasie van het houtparenchym werd niet waargenomen.In Novada bleef de schimmelgroei gedurende het hele experiment beperkt. Macroscopisch waren er enkel lengtescheuren in de stengel te zien, die veroorzaakt bleken te worden door hyperplasie van aan de infectie grenzend houtparenchym. In het geïnfecteerde vaatweefsel optredende gomvorming veroorzaakte ook enige bruinkleuring. In het hyperplastische weefsel werd regeneratie van houtvaten waargenomen. In de stengel werden geen holten gevormd, en verkleuring van de celwanden kwam weinig voor. De vorming van gommen in de houtvaten maakt waarschijnlijk deel uit van het resistentiemechanisme. De daarop volgende houtvatregeneratie is eerder een algemene reactie van de plant op vaatverstopping dan een deel van het resistentiemechanisme.Vaatverbruining, zij het van verschillende oorsprong, komt voor in zowel vatbare als resistente interacties. Om die reden moet men in de resistentieveredeling bij de anjer voorzichtig zijn met het gebruik van bruinkleuring als ziekteïndicatie.     

包心菜无菌苗子叶及叶片原生质体高频分裂和高频植株再生

以包心菜子叶和叶片原生质体为材料。经不同液体培养基(Bp1,Bp2,B1)浅层培养,再生细胞高频分裂并形成愈伤组织。愈伤组织经扩增后转移到分化培养基上诱导植株分化,从这两种原生质体中获得了再生植株。在原生质体培养过程中,原生质体及细胞团的褐化程度与培养基中的有机成分的多少有关。原生质体的分化频率与培养基中植物激素种类关系甚大。在植株分化时,谷氨酰胺和腺嘌呤对植株分化有很大促进作用。另外,原生质体的来源及原生质体培养基对原生质体植株分化能力均有不同的影响。     

‘丰香’草莓叶片高效再生体系的建立

 以草莓主栽品种丰香( Fragaria ×ananassa Duch ‘Toyonoka’) 叶片为外植体, 研究了影响组织培养的多个因素, 建立了高效再生体系。结果表明: MS + TDZ 1.5 mg·L ^{- 1} + IBA 0.4 mg·L ^{- 1}培养基最适于不定芽分化。不同滤光膜(绿膜、红膜、蓝膜、黄膜) 对草莓不定芽的分化具显著效应, 绿膜和红膜对芽的分化有明显促进作用, 不定芽再生率达95%以上, 平均每个外植体再生芽数在25个以上; 而蓝膜和黄膜则不利于芽的分化。不同滤光膜光谱差异主要集中在300～700 nm, 红、绿膜在该波段光强较弱,而黄、蓝膜和荧光灯较强。暗处理4周比1、2、3周更有利于提高叶片的不定芽再生率, 此后转到光下培养, 获得的不定芽再生率可达100%。     

‘过山香’香蕉多芽体的诱导及其体细胞胚的发生

 以我国重要香蕉种质‘过山香’ (AAB) 为材料, 研究了香蕉多芽体诱导、多芽体茎尖薄切片即分生组织性的表层结构物( scalp) 愈伤组织诱导和体细胞胚发生的合适条件。结果表明, 该品种单个不定芽茎尖在P4培养基(含BAP 100 μmol·L ^{- 1}和IAA 1 μmol·L ^{- 1} ) 中继代5个周期后可诱导获得类似花椰菜结构的多芽体。从30 μmol· m ^{- 2} ·s^{- 1}光强, 光/暗周期(16 h /8 h) 培养的多芽体所获得的scalp在添加2,4-D 5μmol·L ^{- 1}和Zeatin 1 μmol·L ^{- 1}的愈伤组织诱导培养基中黑暗培养, 45 d后愈伤组织诱导率可达97.6%。诱导20 d后黄色分生小球体类结节状愈伤组织开始发生, 90～120 d后在分生小球体局部可获得白色或浅黄色松散的胚性愈伤组织(诱导率为17.5% ) 。从胚性愈伤组织诱导的体细胞胚在成熟培养基上培养60 d后体胚萌发率和植株转化率分别为14.5%和11.1%。     

几种抗生素对梨叶片愈伤组织和不定梢诱导的影响

研究了氨苄青霉素(Amp)、羧苄青霉素(Carb)、头孢霉素(Cef)和卡那霉素(Km)对梨叶片愈伤组织和不定梢诱导的影响。结果表明,Amp对巴梨叶片分化影响较小,当浓度达500mg/L时,其出愈率和不定梢再生率分别为96.48%和56.17%,与对照差异不显著;Cef浓度在50-300mg/L时对巴梨和身不知叶片再生均无显著影响,只有当Cef浓度高于400mg/L时,巴梨的不定梢再生率才受到显著抑制;巴梨和身不知叶片对Carb的反应不相同,低浓度(≤200mg/L)的Carb对巴梨的出愈率和不定梢再生率影响较小,却显著抑制身不知的不定梢再生率,高浓度(≥300mg/L)的Carb不仅极显著抑制巴梨和身不知的出愈率,而且完全抑制了2者的不定梢再生;Km浓度大于10mg/L时,明显抑制愈伤组织的生长,且随着浓度的增加,死亡率逐渐增大,当Km浓度达100mg/L时,巴梨和身不知叶片死亡率达100%和96.30%。     

四川‘竹根姜’胚性细胞悬浮系的建立与植株再生

 选用四川省地方品种‘竹根姜’的茎尖组织建立了体细胞胚性细胞悬浮系, 并通过悬浮培养获得了姜再生植株。结果表明悬浮细胞干质量受pH影响。接种量和AgNO₃ 对悬浮细胞的生长都有影响:最佳接种量为1.0% , 最适AgNO₃浓度为6.0 mg·L ^{- 1}。胚性细胞悬浮系增殖后, 接种到前期筛选的成熟分化培养基上获得了再生植株。     

干旱区绿洲荒漠交错带土地退化及生态重建

由于经济的发展，土地资源受到越来越大的压力。当这种压力超过了土地资源的承载能力，就导致了土地退化的发生。作为陆地生态系统的基础，土地资源的退化表现为：土壤肥力降低，生物多样性降低，以及伴随的经济发展的落后。当前世界范围内对土地退化的治理，基本方法仍是基于生态学理论的生物方法。但对土地退化的恢复与生态系统的重建的研究，需要经过谨慎设计的长期实验。绿洲荒漠交错带的重要性，不仅表现为是绿洲的保护屏障，而且在绿洲经济的发展中也起到巨大的作用。通过对国内外大量研究的回顾，讨论了在不同地区进行的长期实验所采用的方法。有人为因素参与的退化土地恢复与生态重建，可以在短期内取得明显效果。产生土地退化的原因，不仅仅是土地资源特点与自然环境这样一些自然因素，还包括一些社会与经济因素。因此退化土地的恢复与生态重建的成功，需要一种考虑自然、社会和经济因素的综合的方法。     

莴苣‘红帆’品种下胚轴愈伤组织诱导与植株再生

 莴苣下胚轴愈伤组织诱导时, MS+ 6-BA 0. 5 mg/ L+ 2, 4-D 1 mg/ L+ NAA 0. 1 mg/ L 效果最好,出愈率达94%; 愈伤组织分化为芽时, MS+ 6-BA 1. 0 mg / L+ NAA 0. 05 mg/ L 分化频率最高, 达100% ; 再生苗在1/ 2MS+ NAA 0. 5 mg/ L 中诱导生根成为完整植株。     

培养条件对酸枣叶片不定梢再生率的影响

以酸枣无菌苗叶片为外植体,选用基本培养基ＮＮ６９和ＷＰＭ,外源激素包括ＴＤＺ、ＩＡＡ、ＩＢＡ和ＮＡＡ,暗培养时间为２、３、４周。采用正交实验设计方法,研究了基本培养基、外源激素及暗培养时间对叶片不定梢再生的影响。结果表明在附加ＴＤＺ１~３ｍｇ/Ｌ的ＷＰＭ和ＮＮ６９上都可诱导不定梢再生,但ＷＰＭ比ＮＮ６９更有效。暗培养时间对不定梢再生也有影响,暗培养３周比２、４周更有利于提高叶片的不定梢再生率。在附加ＴＤＺ１ｍｇ/Ｌ、ＩＡＡ０．１ｍｇ/Ｌ的ＷＰＭ培养基上,暗培养３周后转到光下培养,获得的不定梢再生率达８７．５%。     

Effects of liver regeneration on the proliferation of rat fetal hepatocytes after intrasplenical transplantation

AIM:To study the effect of environment of liver regeneration on the proliferation of rat fetal hepatocytes after intrasplenical transplantation. METHODS:Fetal hepatocytes isolated from 3-week SD rat fetuses bred were transplanted into the spleens of liver regeneration model rats with 70% partial hepatectomy. The cell cycle of the hepatocytes in the remnants liver was analyzed by flow cytometer and the density dimensions of the donor fetal hepatocytes in spleen were measured by image analysis system 7 and 30 days post-transplantation, respectively. RESULTS:Compared with the control group, the proportions of S and G₂ /M cells in the remnants liver were obviously decreased (P＜0.05), but the density dimensions of the donor fetal hepatocytes in spleen increased significantly (P＜0.05) in rats with hepatectomy 7 days post-transplantation. CONCLUSION:The environment of liver regeneration is propitious to the proliferation of fetal hepatocytes after transplantation into spleen.