阔叶林采伐更新技术调查

本文通过系统调查分析三种阔叶林采伐更新方式所形成的林分外貌特征和效益，总结阔叶林采育技术，为科学经营提供依据。     

糙皮侧耳和佛罗里达侧耳菌丝原生质体的形成与再生

本文报道了使用蜗牛酶和纤维素酶从糙皮侧耳和佛罗里达侧耳双核菌丝体中,成功地分离了高产量的原生质体。菌丝体培养时间,混合酶液 pH 值,一定浓度的酶液用量,酶解温度和时间与原生质体形成相关。原生质体的两种再生型被观察到,并计算了再生频率,糙皮侧耳为2.5%.佛罗里达侧耳为2.3%。     

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。     

‘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。     

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.