黄瓜新品种津优12号的选育

用优良自交系Q12作母本,F51作父本配制的一代杂种津优12号,植株生长势中等,叶色深绿,瓜条顺直,长棒状,长35 cm左右;单瓜质量200g左右,瓜色深绿,有光泽,瘤显著,密生白刺,果肉淡绿色,质脆,味甜,畸形瓜率低;春季主蔓第1雌花着生在第4节左右,雌花节率高.春露地栽培产量可达5 500kg·(667m2)-1左右,秋大棚栽培产量4 200kg·(667 m2)-1.抗枯萎病、霜霉病、白粉病和CMV.适宜华北、东北、西北地区春露地和秋大棚栽培.     

夏秋萝卜新品种丰玉一代的选育

丰玉一代是以雄性不育系4-04A为母本，S30—1为父本配制的一代杂种，属夏秋萝卜类型，生育期70～75d（天），肉质根圆柱形，长25—30cm，粗8—10cm，皮色全白，表皮光滑，含水量适中，肉质细密脆嫩，单根质量1，0—1．5kg。每667m^2产量2500kg左右，适宜山西省夏秋季种植。     

辣椒新品种镇江3号的选育

中晚熟杂交一代辣椒镇研3号是以江苏本地羊角椒自交系Y9007为母本,由甘肃酒泉引进的甜椒自交系T9218为父本配制的一代杂交组合。镇研3号为中熟辣椒品种,果形为牛角形,纵径15cm,肩横径5.0cm、肉厚0.40cm,单果平均重42g。果面光滑,青熟果绿色、味微辣,风味佳,适宜在长江流域或南方保护地栽培种植,667m2产量约为4200～5000kg。     

模糊隶属法对玉米苗期耐旱性的拟合分析

在略高于玉米萎蔫系数的干旱条件下,以出苗率和生物学产量耐旱系数之乘积为指标,测定了17个玉米自交系和10个杂交种的苗期抗旱性。并用模糊隶属法,以干旱胁迫下的胚芽鞘长度,出苗率,根重,生物学产量,脯氨酸含量,电导率和离体叶片保水力等指标对各品种耐旱性进行了拟合分析。结果表明,在略高于萎蔫系数的干旱条件下,以出苗率和生物学产量的耐旱系数之乘积为指标,可以准确鉴定玉米苗期的耐旱性,与耐旱性的综合评价拟合良好(相关系数r=0.914)。     

珍黄88(湘椒29号)辣椒的选育

珍黄88的母本6427是从广西地方品种经自交纯化而成的优良黄皮尖椒自交系;父本8215为叶少、部分茎节短缩、肉厚疏松的辣椒高代自交系。该品种中熟,定植至采收青椒约50 d(天),产量2500～2800 kg·(667 m~2)~(-1),抗病毒病,中抗疫病,适于山东、广东等黄皮尖椒外运基地栽培;果实长牛角形,果表黄绿无皱,果型直,肉厚腔小,商品性好,耐贮运。     

日光温室黄瓜济杂3号的选育

母本88001来源于津杂2号,父本88010来源于津研2号与新泰密刺的杂交后代。其一代杂种济杂3号,瓜条顺直,长30～35 cm,单瓜质量约180 g,瓜把短,瓜皮深绿,密瘤白刺,品质优,商品性好,对霜霉病、白粉病、枯萎病抗性强。每667m~2产量7000～14000 kg,适合日光温室越冬茬和早春茬栽培。     

春丰50苦瓜的选育

以曼谷青皮、碧绿1号和钦州大肉苦瓜为育种材料,采用双父本混合花粉杂交和后代系谱选择育成优良自交系,再经配合力测定选出优良一代杂种春丰50。该品种生长势强,果实粗棒形,纵径26.3cm,横径6.45cm,皮色翠绿油亮,一般单果质量420g左右。平均每667m~2产量3 500kg。     

沙漠化过程土壤种子库特征的研究

采用野外定点取样与室内萌发实验相结合的方法 ,研究了 4种不同类型退化沙地土壤种子库特征 ,主要结论是 :(1)土壤种子库密度随沙漠化程度的增加而下降 ,不同沙漠化发展阶段下降速率不同 ,从固定到半固定沙地是种子库密度衰减最快的时期 ;(2 )土壤种子库植物种数从固定到半流动沙地变化很小 ,半流动到流动沙地衰减速度明显加快 ,是种子库植物种数衰减最快的时期 ;(3) 4种类型退化沙地土壤种子库的种类组成以 1、2年生草本植物为主 ,所占比例 79%～ 88% ,多年生草本和灌木所占比例很小 ;(4 )土壤种子库物种多样性指数并非随着沙漠化程度的增加而下降 ,其中半流动沙地的物种多样性指数最小 ;(5 ) 4种类型退化沙地土壤种子库组成上的相似性系数变化范围为 0 .82 9～ 1.0 0 0 ,表现出较小的空间异质性。     

Biological and Physical Constraints on Maize Production in the Humid Forest and Western Highlands of Cameroon

The aim was to identify biological and physical factors responsible for reducing maize yield in Cameroon. Two surveys were conducted in 137 fields in two agroecological zones in 1995–1997. In the Humid Forest (HF), Bipolaris maydis, Stenocarpella macrospora, Puccinia polysora, Rhizoctonia solani and soil fertility were factors that reduced maize production in 1995 and 1996. In the Western Highlands (WHL), Cercospora zeae-maydis, and the interaction between soil fertility and maize variety were the most important constraints to maize production in 1996. In 1997, C. zeae-maydis, S. macrospora, physiological spot and stem borer damage (Busseola fusca) were negatively related to ear weight. The combination of these biological factors (diseases and insects), and the physical parameter of soil fertility were responsible for reducing maize yield in these selected benchmarks of Cameroon. Maximum potential yield reductions were estimated at 68% due to B. maydis and 46% due to S. macrospora, respectively, in the HF in 1995. In 1996, maximum potential yield reductions in the HF were estimated at 34%, 41% and 30% due to S. macrospora, P. polysora and R. solani, respectively. In the WHL, C. zeae-maydis had the potential to cause a yield reduction of 79% in 1996. In the WHL in 1997, the interaction between C. zeae-maydis and B. fusca, stem diseases and the physiological spot caused potential reductions of 52%, 34% and 39%, respectively.     

Variation in the development of secondary dormancy in oilseed rape genotypes under conditions of stress

Summary A substantial amount of seed is left in the fields before and during harvest of oilseed rape. Although this crop exhibits little or no primary dormancy, the absence of certain environmental cues that promote germination of imbibed seeds induces secondary dormancy. The work reported investigated the extent to which environmental stress conditions, including osmotic stress, low oxygen stress and anaerobiosis, induce secondary dormancy in oilseed rape, and examined the variation in development of secondary dormancy between and within genotypes. Osmotic stress was most effective in inducing dormancy. Anaerobic treatment produced very few dormant seeds, as did an atmosphere low in oxygen and high in nitrogen. The development of secondary dormancy under osmotic stress varied considerably between and within genotypes. Dormancy ranged from almost zero to about 60% for winter genotypes and about 85% for spring types. Within genotypes, variations occurred between seed lots and years of harvest. Temperature variations affected the percentage of dormant seeds. More dormant seeds were likely to be produced with incubation under water stress at 20 °C than at 12 °C. In winter genotypes, fewer dormant seeds were produced when incubation temperature and germination test temperatures differed. Thus, incubating at 20 °C and 12 °C, followed by germination tests at 20 °C and 12 °C, respectively, produced most dormant seeds. Also, in the winter genotypes, the potential development of secondary dormancy was positively correlated with the pattern and speed of germination of untreated seeds.