高寒冻土层地区不同土壤改良措施对花叶海棠光合特性的影响

为促进花叶海棠在天峻县的生长,采用不同比例的森林土、泥炭、腐熟羊粪、河砂和珍珠岩改良土壤,分析不同土壤改良措施下花叶海棠叶片的净光合速率、蒸腾速率、气孔导度及胞间CO_2浓度。结果表明:在6个处理中,S_3(50%森林土+10%泥炭+10%腐熟羊粪+5%河砂+5%珍珠岩+20%原土)、S_2(40%森林土+10%泥炭+10%腐熟羊粪+5%河砂+5%珍珠岩+30%原土)处理的叶片平均净光合速率较大,分别为14.11μmol m~(-2)s~(-1)、13.72μmol m~(-2)s~(-1),增长率分别为17.58%、14.32%;S_3、S_6(10%森林土+50%泥炭+10%腐熟羊粪+5%河砂+5%珍珠岩+20%原土)处理的叶片平均蒸腾速率较大,分别为12.44mol m~(-2)s~(-1)、11.64mol m~(-2)s~(-1),增长率分别为65.65%、54.99%;S_6、S_3处理的叶片平均气孔导度较大,分别为0.455mol m~(-2)s~(-1)、0.426mol m~(-2)s~(-1),增长率分别为49.18%、39.68%;S_3处理的叶片平均胞间CO_2浓度较大,为280.1μmol mol~(-1),增长率为21.10%;不同土壤改良措施与花叶海棠叶片的净光合速率、蒸腾速率及胞间CO_2浓度均呈极显著性相关(P0.01),与气孔导度呈显著相关(P0.05),经各项指标综合分析,筛选出经S_3处理的试验地最适宜花叶海棠生长。     

几种木本园艺植物塑料袋内密封扦插试验

本文报道在食品保鲜袋内密封扦插桂花、樱花、甜樱桃和苹果的试验结果。当年生半木质化至完全木质化插条经生根促进剂处理后，密封扦插在食品保鲜袋内的湿润基质上，放置空旷处，夏秋高温季节晴天适度遮阴。结果表明，塑料袋内的温度较稳定，基质始终保持刚扦插时的湿润状态，插条叶片全部或部分保持饱满、挺立。插条一周左右即可产生愈伤组织，３─４周便可出根。尽管在几种材料上获得的生根率差异较大，但都成功地生了根。在以“峨嵋仙土”为扦插基质，６月份晴天１０：００─１７：００时遮阴的条件下，樱花的生根率达７０％以上。     

新疆野苹果叶形性状变异及其与SSR标记关联分析

以从新疆天山地区新疆野苹果600个无性系中筛选得到的18个优系为研究对象,调查其叶形性状变异,并进行了SSR分子标记分析,探究叶形性状与SSR标记间的相关关系。结果表明,调查的15个叶形性状在无性系间均存在极显著差异;平均变异系数最大的为叶尖角α(达到25.39%),叶形指数L1/L3最小(仅为10.31%);叶片长的重复力最大(达到0.967),叶形指数L1/L3最小(仅为0.495)。以15个叶片性状为依据,可将各无性系完全区分开,并分为3类,各无性系间的遗传距离变化在1.293~7.235间。用均匀分布在17个染色体连锁群上的30对多态性SSR引物对18个无性系进行聚类分析,可将各无性系完全区分开,并可分为4类,各无性系间的遗传距离为0.089~0.689,平均遗传距离为0.433。所有叶形性状聚类结果与所有SSR标记聚类结果不相关。以单一叶形性状聚类结果与经过筛选的部分SSR标记聚类结果进行相关分析,绝大部分达到极显著相关,且大部分引物组合表现为累积效应,表明叶形性状与部分SSR位点具有紧密关联。     

Cytoplasmic relatedness of apple landraces and cultivars: a molecular analysis

Summary Mitochondrial DNA (mtDNA) diversity has been determined in apple landraces and cultivars, based upon restriction fragment length polymorphisms (RFLPs) for several mitochondrial genes. Our analysis includes three cultivars, Golden Delicious, McIntosh and Delicious, which represent the various patterns of mtDNA polymorphisms previously described (Ishikawa et al., 1992). A total of five RFLPs were detected, allowing classification of the apple genotypes into four cytoplasmic groups: GroupI, Golden Delicious-type; GroupII, McIntosh-type; GroupIII, Delicious-type; and Group IV, Dolgo Crab-type. European landraces and cultivars were assigned to Groups I, II, and III, while chinese crab apples were placed in either Group III or IV.     

Identification of PCR-based markers linked to the powdery-mildew-resistance gene Pl1 from Malus robusta in cultivated apple

The availability of molecular markers linked to mildew resistance genes would enhance the efficiency of apple-breeding programmes. This investigation focuses on the identification of random amplified polymorphic DNA (RAPD) markers linked to the Pl₁ gene for mildew resistance, which has introgressed from Malus robusta into cultivated apples. The RAPD marker technique was combined with a modified ‘bulked seg-regant analysis’ mapping strategy. About 850 random decamer primers used as single primers or in combinations were tested by PCR analysis on the basis of resistant and susceptible DNA pools. Selected primers producing RAPD fragments were applied in an additional selection step to M. robusta and genotypes representing intermediate breeding stages of the breeding population 93/9, for which a 1:1 segregation could be observed for the resistance trait. Seven RAPD markers, all representing introgressed DNA sequences from M. robusta, were identified and arranged with the Pl₁ locus in a common linkage group. The two most tightly-linked RAPD markers, OPAT20₄₅₀ and OPD2₁₀₀₀ were mapped with a genetic distance of 4.5 and 5 cM, respectively, from the Pl₁ gene. Both markers are suitable for marker-assisted selection in apple breeding. The polymorphic DNA fragment OPAT20₄₅₀ was cloned and sequenced, and longer primers for the generation of a sequence-characterized amplified region (SCAR) marker have been constructed; this marker was easier to score than the original RAPD marker.     

Screening fruit tree genetic resources in Belgium for disease resistance and other desirable characters

Summary The wide diversity of old fruit-tree cultivars originating or introduced into Belgium during the 18 ^th and 19 ^th centuries was collected as far as feasible over the last fifteen years at the State Plant Pathology Station in Gembloux. Out of the 2400 accessions now collected, one quarter was recovered from old public collections, and three quarters came from farms or gardens. The initial intention was to screen the material for disease resistance and other characters of agronomic interest with a view to using the best cultivars as breeding parents. However, as the collection developed, genetic resources conservation also became an objectiveper se. The collection presently contains 1150 apple, 850 pear and 300 plum accessions, and smaller numbers of other fruit species. Each accession is evaluated in an experimental orchard for at least ten years. In view of the growing public interest in old fruit-tree cultivars, the Plant Pathology Station has for several years been releasing to the nursery trade the better cultivars emerging from the evaluation, namely nine apple and four plum cultivars, and one peach cultivar. The principal features of the apple cultivars are presented in this paper. Since 1988, old apple and plum cultivars have been being used at the Station as parents in a breeding programme, with both controlled and open pollination. In some instances, old apple cultivars have also been crossed with a modern parent carrying the Vf gene for scab resistance. The preliminary observations on some of these seedlings are presented.     

Identification of marker alleles linked to fire blight resistance QTLs in apple genotypes

Molecular marker analysis can be an effective tool when searching for new fire blight resistance donors. It can speed up the breeding process as well, even though many of the available markers linked to fire blight resistance QTLs have not yet been tested by screening a large number of cultivars. The aim of this study was to search for alternate sources of the three major QTLs of fire blight resistance; FBF7, FB_MR5 and FB_E, as well as to test the efficiency of some markers linked to minor QTLs. Altogether, nine primer pairs were used on 77 genotypes including new Hungarian cultivars and old apple cultivars from the Carpathian basin. Several marker alleles of FB resistance QTLs have been detected in the screened genotypes, most importantly the alleles coupling with FB_MR5 in the old cultivars ‘Kéresi muskotály’, ‘Szabadkai szercsika’ and ‘Batul’. We propose these cultivars as the first available resistance donors of FB_MR5 instead of the crabapple Malus × robusta 5. The results also bring new information regarding the resistance alleles of new Hungarian cultivars and selections.     

用RAPD和SSR分子标记鉴定小金海棠F1代 杂种实生苗的研究

小金海棠（Malus xiaojinensis）具有多种抗逆特性，是苹果属植物中一种珍贵的野生种质资源。由于小金海棠具有无融合生殖特性，早期准确、快速、有效地鉴定其F1代杂种实生苗对于研究利用其众多抗逆基因具有重要意义。RAPD技术是现有鉴定果树杂种实生苗最为简单、快速和有效的分子标记技术，但RAPD技术本身存在一定的不稳定性。笔者对小金海棠和山荆子（M. baccata）F1代杂交实生苗79个单株进行了RAPD分析，并用SSR标记对RAPD标记的初步鉴定结果进行了进一步的验证。结果显示，RAPD标记鉴定出的杂种实生苗有72.2%得到SSR标记的证实。研究的结果还表明，“叠加”和“新带”两种RAPD带型，结合RAPD标记特异位点数可以为小金海棠F1代杂种实生苗提供可靠的鉴定依据。研究为利用RAPD技术早期快速鉴定果树杂种实生苗提供了新的信息和依据。     

Mitochondrial DNA Restriction Fragment Length Polymorphisms in Malus Species

Three apple (Malus×domestica) cultivars and 11 Malus accessions have been investigated by the probe hybridization method on their mitochondrial DNA (mtDNA). The gene probes used were: coxI, coxII, atpA, atp6, and atp9. Our results revealed enough variation to characterize ten mtDNA haplotypes among the Malus genotypes examined. The taxonomic and phylogenetic implications of mtDNA polymorphism are also discussed.     

干旱胁迫诱导新疆野苹果细胞程序性死亡的细胞形态学研究

用聚乙二醇(Polyethylene glycol,PEG6000)处理新疆野苹果(Malus sieversii(Ledeb)Roem.)幼苗。通过对其叶片及根系中各细胞器的超微结构分析发现,干旱胁迫能诱导新疆野苹果发生细胞程序性死亡,并具有以下特点:随着干旱处理时间的延长,根系中各细胞器形态结构发生变化的时间普遍早于叶片;同是叶片,海绵组织中各细胞器形态结构发生变化的时间早于栅栏组织;同是根系,皮层细胞中各细胞器形态结构变化的时间普遍早于中柱细胞。