Production,survival and evaluation of solid-substrate inocula ofConiothyrium minitans againstSclerotinia sclerotiorum

Coniothyrium minitans grew on all ten solid-substrates (barley, barley-rye-sunflower, bran-vermiculite, bran-sand, maizemed-perlite, millet, oats, peat-bran, rice and wheat) tested, producing high numbers of germinable pycnidiospores (1.9–9.3×10⁸ g^–1 air dry inocula). All solid substrate inocula survived better in the laboratory at 5 and 15 °C than at 30 °C for at least 64 weeks.In pot bioassays carried out in the glasshouse and field, soil incorporations of each inoculum almost completely inhibited carpogenic germination ofS. sclerotiorum. In the field bioassay, no sclerotia were recovered after 38 weeks fromC. minitans-treated pots compared to 56% from control pots. In the glasshouse bioassay, 9–30% of sclerotia were recovered after 20 weeks fromC. minitans-treated pots, but 88–100% of these were infected by the antagonist. The antagonist also spread to infect sclerotia in control pots.In larger scale glasshouse trials, single preplanting soil-incorporations of five inocula (barley-ryesunflower, maizemeal-perlite, peat-bran, rice and wheat) controlled Sclerotinia disease in a sequence of lettuce crops, with only small differences between the types of inocula tested. At harvest,C. minitans reduced sclerotial populations on the soil surface and over 74% of sclerotia recovered fromC. minitans-treated plots were infected by the antagonist.C. minitans survived in soil in all solid-substrate inocula-treated plots for at least 39 weeks at levels of 10⁴–10⁵ colony forming units cm^–3 soil and spread to infect over 36% of sclerotia recovered from control plots.     

The induction of 1,3-β-glucanases and other enzymes in groundnut leaves infected with Cercospora arachidicola

Infection of groundnut leaves with the early leaf spot pathogen Cercospora arachidicola leads to a marked increase in extracellular 1,3-β-glucanase activity, limited to the infected tissue. Three isoforms of low molecular weight and extreme pI values, typical of pathogenesis-related proteins, were induced. These β-glucanases, when acting together, were capable of degrading the pathogen cell wall in vitro. Glucanases from homogenates of infected leaf tissue were partially purified by ion-exchange chromatography to give enzymes with molecular weights of 35, 32 and 20 kDa and pI values of 3·8, 3·6 and > 9, respectively. They were electrophoretically identical to the β-glucanases found in the intercellular washing fluid. Treatment of groundnut plants with 200 μM mercuric chloride induced the accumulation of identical extracellular β-glucanases. During the course of the infection an increase in peroxidase activity was also observed, but chitinase activity remained more or less constant.     

Fusarium moniliforme secretes four endopolygalacturonases derived from a single gene product

Extracellular endopolygalacturonase, purified from the pathogenic fungus Fusarium moniliforme, consists of four molecular forms (38, 41·5, 45, and 48·5 kDa, respectively. Three forms (38, 41·5, and 45 kDa) were purified to homogencity by FPLC on a Mono S column followed by electroelution after SDS-PAGE. The N-terminal amino acid sequences of each of the three forms, and of a mixture containing all four forms were shown to be identical to that predicted from the nucleotide sequence of the endopolygalacturonase gene previously cloned from F. moniliforme. Enzymatic deglycosylation experiments revealed the presence of N-linked, high mannose oligosaccharide side-chains on all four forms of endo polygalacturonase. Hydrogen fluoride catalysed chemical deglycosylation of the polygalacturonase mixture yielded a single polypeptide with an apparent molecular mass of 36·2 kDa. Southern blot analysis, carried out at high stringency with an endopolygalacturonase-specific probe on genomic DNA digested with three different restriction enzymes, showed a single hybridizing restriction fragment in all three digests. A single 2·0 Mb chromosome hybridized with the endo polygalacturonase-specific probe, as shown by Southern blot analysis of F. moniliforme chromosomes separated by CHEF electrophoresis. Northern blot analysis revealed only one mRNA species 1350 nt encoding endo polygalacturonase. These data indicate that a single gene encodes the endopolygalacturonases of F. moniliforme.     

农作物重要病原菌颉颃菌的筛选

从全国6省12个地区的26种植物根围采集到土壤样本50份。经室内分离、纯化后得到以芽孢杆菌为主的细菌菌株226个。以水稻、小麦和棉花等6种农作物上主要病原菌(8种真菌,4种细菌)为指示菌对这226个菌株进行平板双培养法抑菌测定,分别筛选到至少对1种病原真菌或细菌有颉颃活性的菌株95个和78个。对进一步研制防治不同作物病害的生物制剂建立了一个颉颃菌资源库。     

Presence of cervical vertebral malformation in Dobermann puppies and the effects of diet and growth rate

OBJECTIVE: To investigate the relationship between diet, growth rate and the presence of caudal cervical malformation in Doberman puppies. DESIGN: A prospective study of 15 Dobermann puppies from three unrelated litters, aged from 0 to 16 weeks. PROCEDURE: The growth rate in terms of body weight gain and increase in ulna length were measured weekly for all puppies. In addition the nutritional quality of the diets was assessed. Radiographs of the cervical spine were taken at 6 and between 12 and 16 weeks of age and examined for the presence of caudal cervical vertebral malformation. A mixed model for repeated measures data was used to investigate the relationship between the growth rate of the puppies and the fixed effects age, dam, diet, gender and presence of caudal cervical malformation. RESULTS: Five of the puppies had changes consistent with caudal cervical malformation. The diets fed were either balanced or transiently deficient in protein, calcium, phosphorus and/or magnesium. There was no significant association between growth rate and the variables dam, gender and the presence of caudal cervical vertebral malformation. There was no significant association between diet and increase in ulna length, but a trend existed between body weight gain and the feeding of a balanced diet (P = 0.0672). CONCLUSION: Caudal cervical vertebral changes can be detected radiographically as early as 6 weeks of age in some Dobermann puppies. A balanced diet and growth rate are not significant factors in its initial development.     

Variation of pesticide concentration in sheep dips operated according to traditional and revised methods

OBJECTIVE: To quantify stripping in traditional dipping operations and to revise dipping methods, based on prediction of stripping so that a more stable concentration of pesticide in the dipwash is achieved. DESIGN AND METHODS: Plunge and shower dips were operated sequentially according to traditional and revised dipping instructions. Dips were operated by continuous and intermittent replenishment. Samples of mixed dipwash were collected periodically and assayed for pesticide (diazinon) concentration. RESULTS: Diagrammatic representations of pesticide concentration versus number of sheep dipped indicated traditional dipping leads to wide variations in the concentration of pesticide in dipwash during dipping. Intermittent replenishment led to a 'saw-tooth' pattern in the pesticide concentration. Traditional continuous replenishment (using the starting concentration of pesticide) indicated both the rate and extent of stripping was higher in shower dipping. If sufficient sheep were dipped, equilibrium was reached between the rate of pesticide replenishment and removal. An alternative method of dip operation by continuous replenishment, using a low starting concentration of pesticide and a replenishment concentration high enough to offset the pesticide loss through stripping resulted in a more stable concentration of pesticide in the dip. CONCLUSION: Revision of dipping instructions can lead to exposure of sheep to stable concentrations of stripping pesticide during dipping.     

Water Requirements of Safflower Entries in Middle Egypt

Two promising selected land races of safflower ( Carthamns tinctorious L.) designated as line 11 and line 13, together with the local variety Giza 1 , were examined under three levels of moisture depletions, i.e. 40, 60 and 80 % ASMD at Fayoum, Middle Egypt during 1986/87 and 1987/88 seasons. In both growing seasons, the second irrigation treatment i.e. 60 % ASMD gave the highest means for growth characters as well as seed yield and most of its components. Seed oil content per cent exhibited an increased as soil moisture depletion increased with no significant difference between entries. Safflower entries showed clear differences in some yield components which compensate each other and resulted in no significant difference in seed yield per hectar.
Consumptive use of water by safflower plants increased as the available soil moisture around the root zone increased. No significant differences were found in water consumed by safflower entries used in all experiments.
In the two experimental seasons, the best water use efficiency (WUE) for seed production was obtained also from the second treatment (60 % ASMD). The line 11 gave the best WUE.     

甘蓝型低芥酸油菜单株产量基因效应的研究

用5×5半双列杂交研究甘蓝型低芥酸油菜单株产量的遗传,结果表明:供试的甘蓝型低芥酸油菜品系中,单株产量的遗传符合加性显性模型,显性性质为超显性,平均显性度为1.404。显性基因约为隐性基因的3倍多,并且多数增效基因表现显性,但也有显性的减效基因存在。单株产量的广义遗传力h_B~2=71.4％,狭义遗传力h_N~2=33.18％。供试亲本显性效应的强弱依次为81007>81006>81018>81004>81033,增效基因的多少依次为81018>81006>81007>81004>81033。一般配合力的大小依次为81018>81006>81004>81033>81007。     

使用AoBe处理不同生育期春小麦的增产效应

使用芳氧基乙酸万酯类化合物AoBe处理不同生育期春小麦,在低浓度条件下有促进幼苗生长、提高田间出苗率、刺激增产等生理作用,在高浓度条件下有抑制生长和致死作用。可见,AoBe具有植物生长调节剂的基本作用特性。AoBe刺激增产作用的适宜处理时期和浓度范围是:浸种和挑旗期为0.01ppm,分蘖期为0.1ppm,拔节期为1 ppm,抽穗期为100ppm左右。以0.01ppm浸种和0.1ppm在分蘖期喷施为最佳组合。1000ppm处理春小麦种子则表现为致死作用。     

Morphologic evaluation of acute endometritis in mares with differing resistance to uterine infections

The study was designed to determine differences between normal mares and mares with endometrial pathology in the inflammatory response after bacterial challenge. Six normal mares (biopsy category I) and 4 mares with pathological endometrial changes (biopsy category II) were given an intrauterine infusion of β-hemolytic streptococci on the second day of estrus. All mares had a similar kind of inflammatory response after the bacterial inoculation as assessed by rectal and vaginal examinations. There were no significant differences in the amount of discharge, uterine tone, uterine size and cervical relaxation between the groups. Leukocytic response, as determined by endometrial smears and biopsies, was of the same magnitude in both groups. Two mares from the pathological group were not able to eliminate the infection, but had vaginal discharge and bacteriologically positive uterine swabs until the end of the experiment. It is concluded that the inability of some mares to clear uterine infections cannot be explained by a deficient inflammatory response.