北疆苜蓿属植物繁育系统的研究

采用等位酶技术，对北疆苜蓿属植物种群的繁育系统进行了研究。结果表明，北疆苜蓿属植物种群为外繁育系统，黄花苜蓿、多变苜蓿、紫花苜蓿基因组成中杂合体过多，均保持较低的自交结实率。参试苜蓿属植物表现某种程度的内繁育衰退现象，地理或生殖隔离等因素可能是导致个别种群出现内繁育衰退现象的原因之一。对北疆苜蓿属遗传资源保护时，既要选择遗传基础丰富的种和种群以保持最多的遗传变异，还要注意选择具有不同等位的种群以保持原有的基因和基因频率。     

湖南马尾松遗传改良现状与策略

在叙述湖南马尾松20多年来于马尾松群体遗传改良、马尾松优良家系定向选择、马尾松基因资源收集与种子园营建等方面所取得成绩的基础上，探讨了目前马尾松遗传改良所存在的问题，提出了今后一段时期湖南马尾松遗传改良策略。     

应用数码育种新方法改良晋番茄1号

数码育种是作者根据十几年的育种经验总结出的一套育种新方法。实践证明,应用该方法使育种目标更明确,育种路线更正确,选配组合更精确,育种路径更快捷,克服了选配组合的随机性和盲目性,能够在最短的时间内,以最少的投入,达到预期的育种目标。     

Morphological characterization of the interaction between Diplocarpon rosae and various rose species

Blackspot, caused by Diplocarpon rosae , is the most severe and ubiquitous disease of garden roses, but information is lacking about genotype-specific forms of resistance and susceptibility of the host. Macro- and microscopic analyses of 34 rose genotypes with a defined monoconidial culture black spot inoculum identified susceptible and resistant rose genotypes and further genotype-specific subdivisions, indicating the presence of partial forms of resistance and different resistance mechanisms. In total, eight interaction types were characterized, five representing compatible (types 1–5) and three representing incompatible interactions (types 6–8). The incompatible interactions were characterized by the lack of any visible fungal structures beneath the cuticle (type 8), single-cell necroses (type 7) or necroses of larger cell clusters (type 6), the latter two types with penetration hyphae and haustoria in epidermal cells.     

溴隐停对惠州麻肉种鸡产蛋性能的影响

研究目的在于探讨多巴胺受体激动剂(溴隐停)对地方良种肉鸡繁殖性能的影响。方法从628只28周龄健康的“惠州麻”黄羽肉种鸡群中随机选取1组鸡笼内的40鸡作为实验组,其余的作为对照组。实验组鸡群喂服溴隐停,每只鸡每天1.25mg,连用4d,停用4d后再用4d,对照组不使用。结果在4周的实验期内实验组和对照组的产蛋率分别为83.86%和69.96%;破蛋率分别为1.28%和1.69%,畸形蛋率分别为4.33%和1.19%;实验组平均每只鸡的产蛋总数比对照组多3.89个、合格种蛋数多3.26个;药物处理对平均蛋重无显著影响;使用溴隐停能够提高鸡血液中的雌激素水平。结论溴隐停能够通过抑制地方良种肉鸡体内促乳素的合成与分泌,减少抱窝现象的发生,提高其繁殖性能。     

桑树新品种育71-1的育成初报

育71—1是通过杂交、单株选择、株系选择和品比试验等一系列选育程序,培育成功的新桑树品种。其主要经济特性与湖桑32号相比,发芽期早2—3天,发芽率提高28.7％,产叶量提高47.7％,叶质较优,丝质成绩相仿;抗旱性较强。目前,正在江苏的海安、溧阳及山东等部分地区试种。     

Preliminary results of using in vitro axillary and adventitious buds in mutation breeding of Chinese gooseberry

Summary Aseptically cultured shoots of Chinese gooseberry exhibited growth disorder and morphological aberrances, and some died after being exposed to sufficient gamma-ray irradiation. The death rate was dose dependant and the LD₅₀ was 80–90 Gy and 50–60 Gy respectively for cv. Hayward and clone 4. All petiole explants irradiated with gamma-ray could form calli as the control, but the rate of differentiation of adventitious shoots of the petiole explants decreased and was dependant on dose. Sensitivity of the shoot or petiole explants to gamma-ray irradiation varied with species. Gamma-ray irradiation did not deter either the 2-node segments from producing axillary shoots M₁, M₂, and M₃ or the advantitious shoots originating in the petiole explants and the M₃ shoots from forming advantitious roots. Therefore, using aseptically cultured axillary or adventitious buds for mutation breeding of Chinese gooseberry is feasible. A bacterium surviving in the explants lessened the efficiency of these two in vitro techniques in mutation breeding of Chinese gooseberry.Abbreviations IAA 3-indole acetic acid - IBA -indole butyric acid - MS Murashige & Skoog (1962)     

转基因苜蓿研究进展

就苜蓿基因工程在育种上的研究、转基因技术在苜蓿上的进展做了简要介绍。     

Detection of the Defoliating Pathotype of Verticillium dahliae in Infected Olive Plants by Nested PCR

Spread of Verticillium wilt into newly established olive orchards in Andalucía, southern Spain, has caused concern in the olive industry in the region. This spread may result from use of Verticillium dahliae-infected planting material, which can extend distribution of the highly virulent, defoliating (D) pathotype of V. dahliae to new areas. In this study, a molecular diagnostic method for the early in planta detection of D V. dahliae was developed, aimed especially at nursery-produced olive plants. For this purpose, new primers for nested PCR were designed by sequencing a 992-bp RAPD marker of the D pathotype. The use of the specific primers and different nested-PCR protocols allowed the detection of V. dahliae pathotype D DNA in infected root and stem tissues of young olive plants. Detection of the pathogen was effective from the very earliest moments following inoculation of olive plants with a V. dahliae pathotype D conidia suspension as well as in inoculated, though symptomless, plants.