存款保险制度对农村中小金融机构影响分析

存款保险制度对于保护中小储户的利益、维护金融稳定有着积极的作用,但存款保险制度容易产生道德风险和逆向选择,因此科学合理地设计存款保险制度的具体内容至关重要。农村中小金融机构有必要纳入存款保险体系中,但是对其征收保费费率要控制在较低水平之内。     

谈中小桥采用后张法16m预应力空心板的施工问题

本文阐述了中小桥上部结构采用后张法１６ｍ预应力空心板的施工时应注意的问题，如预应力空心板的预制中底模的施工；侧模、蕊模；砼的要求；浇筑空心板的具体步骤。     

以大蜡螟与人工培养基连续传代的两种斯氏线虫生物学特性比较

本文比较了 Steinernema carpocaprae 和 Steinernema anomali 两个种(品系)的斯氏昆虫病原线虫,分别在大蜡螟和鸡什海绵人工培养基下连续传代培养的两个种群的形态、带菌率、发育、繁殖、毒力和寻找寄主能力的差异。试验表明:同一种(品系)长期在蜡螟传代的线虫种群比人工培养基传代的种群的线虫体较大,在寄主昆虫内发育怏、繁殖量大。但细菌保留率、感染率、感染指数、在沙里寻找寄主并使其致死的能力稍低。上述的差异在 S.anomali 这个种尤为明显,S.car pocapsae 则差异不大。     

Application of polyclonal and monoclonal antibodies for the detection of Xanthomonas campestris pv. campestris in crucifer seeds using immunofluorescence microscopy

Polyclonal and monoclonal antibodies (PCAs and MCAs) were tested for the detection ofXanthomonas campestris pv.campestris (Xcc) in cabbage seeds using immunofluorescence microscopy (IF). It was concluded that PCA 94, MCAs 20H6, 2F4, 18G12 and a mixture of MCAs 20H6, 18G12, 2F4 and 16B5 could be used to detect Xcc in seed extracts when 5 min and 2.5 h shaking of seeds are used as extraction methods. The reliability of confirming suspect colonies with MCAs and PCA 94 in IF depended in part on the seed lot tested and the antibody used. Some virulent Xcc strains derived from seed lots, did not react with MCAs 10C5, 2F4, 18G12, 17C12 and 16B5. On the other hand, saprophytic isolates obtained from one seed lot cross-reacted with MCA 17C12 and to a lesser extent with MCAs 2F4, 18G12 and PCA 94. No relationship was found between IF-reactions of Xcc strains using MCAs and reactions of Xcc strains in pathogenicity testing. Xcc andX. c. pv.amoraciae (Xca) could in general not be distinguished on the basis of reactions with MCAs and PCAs. Also in pathogenicity tests Xcc and Xca were hard to distinguish.     

菌根性食用菌栽培研究进展

对目前菌根性食用菌栽培研究的进展进行了综述。重点介绍了菌根性食用菌与共生植物的相互作用,几种主要菌根性食用菌的培养条件、接种方法和栽培方法,以及种植园管理技术的研究现状。     

Hybridization and in vitro culture of an orchid hybrid Ascocenda ‘Kangla’

The present study focuses on hybridization program involving two species belonging to two different vandaceous genera, viz., Ascocentrum ampullaceum (Roxb.) Schltr. var. auranticum, a narrow endemic orchid of Manipur and Vanda coerulea Griff., an endangered orchid of Appendix I of CITES (Convention on International Trade in Endangered Species of Wild Fauna and Flora), to synthesize the primary hybrid genus with intermediate and improved characters in the F₁ generation. Observations on the crossability in the present bigeneric cross between V. coerulea and A. auranticum had been achieved with 60% success when V. coerulea was taken as female parent. Murashige and Skoog (MS) basal medium at half-strength was effective for the development of the hybrid seedlings of V. coerulea × A. auranticum followed by Vacin and Went (VW) and Knudson C (KC) media. The best response of seedling growth was observed on MS medium at half-strength supplemented with 2.3 μM kinetin + 0.5 μM α-naphthalene acetic acid with maximum shoot height (2.7 cm), leaf number (4.6) and root number (4.1) after 150 days of inoculation. The survival percentage and growth performance of the seedlings were found to be higher (80% survival) in potting substrate consisting of brick:charcoal in the ratio 2:1 mulched with moss (Sphagnum sp.) than in potting substrate consisting of brick:charcoal:tree fern in the ratio 2:1:1. The first flowering was observed in the hybrid seedlings of V. coerulea × A. auranticum after 2 years of transfer to the ex vitro environment. Morphologically, the flowers differed from that of the parents clearly showing the success of the hybridization experiment. Registration of the hybrid has been made with the Royal Horticultural Society with the nomenclature Ascocenda ‘Kangla’ (No. T128725).     

牛肝菌胞外多糖发酵培养基的优化

以美味牛肝菌为研究对象,对其多糖发酵主要影响因子和发酵培养基优化进行研究.通过对单因子培养基优化处理试验结果的分析比较,选择出3个对牛肝菌多糖发酵影响较大的因子进行了正交试验,结果表明:美味牛肝菌最适培养基为20.0g葡萄糖 7.0g酵母粉 3.0g黄豆粉 1.0gKH2PO4 0.5g MgSO4·7H2O 0.5 gMnSO4·H2O.     

动物肠道益生菌地衣芽孢杆菌的筛选及培养基的优化

为了研制新型微生态制剂,以常用益生菌株--地衣芽孢杆菌（Bacillus licheniformis）为试验菌株,在测定了初发菌株的极限耐受性后,运用紫外诱变技术筛选到了一株耐酸性较强,耐胆汁,耐高温的地衣芽孢杆菌D-11.其极限耐受条件为：pH 4.18,胆盐浓度0.4 g/L,温度58 ℃.并通过试验对该菌株进行了形态和生理生化特征的鉴定.最后通过单因素和正交试验对地衣芽孢杆菌D-11的发酵培养基成分配比进行了选择和优化,为以后的工业化生产提供依据.结果显示当培养基的配比浓度为：玉米淀粉15 g/L、豆粕粉90 g/L、玉米浆6 g/L时菌体的培养效果最好.     

High frequency plantlet regeneration from callus and artificial seed production of rock plant Pogonatherum paniceum (Lam.) Hack. (Poaceae)

Pogonatherum paniceum (Lam.) Hack. is a rock plant with good potential for vegetative recovery on naked lands. A high frequency in vitro regeneration system was developed for P. paniceum. Calli were induced from explants of mature seeds, seedlings, young leaves, and stem segments on Murashige and Skoog (MS) medium supplemented with 1.0 mg L⁻¹ 2,4-dichlorophenoxyacetic acid (2,4-D), 2.0 mg L⁻¹ α-naphthalene acetic acid (NAA) and 0.2 mg L⁻¹ 6-benzylaminopurine (BAP). High induction rates (59.57%) and regeneration rates (100%) were obtained from mature seed explants; calli were sub-cultured for over 2 years and still retained a high regenerative capacity. One seed explant resulted in 69,997 plants in 1 year. Shoot buds derived from calli were used for encapsulation in liquid MS medium containing 3% sucrose and two different alginate matrices (3% sodium alginate (w/v) + MS medium containing 3% sucrose and 3% sodium alginate + 1% activated carbon (w/v) + MS medium containing 3% sucrose) with a 20-min exposure to 2% CaCl₂ and 0.3% bavistin (w/v). The capsule with 3.0% sodium alginate (w/v) and 1% activated carbon (w/v) showed a higher conversion rate (61.58%) and stronger plantlets under non-aseptic conditions. These systems are useful for the rapid clonal propagation and dissemination of artificial seed material of P. paniceum for eco-recovery.     

Cryopreservation of carnation (Dianthus caryophyllus L.) shoot tips by encapsulation-vitrification

Shoot tips excised from in vitro cultured plants of Dianthus caryophyllus L. (cv. Pallas, cv. Pink Candy and cv. Wanessa) were successfully cryopreserved using an encapsulation-vitrification method. Shoot tips (2–3 mm in length) were encapsulated in sodium alginate, precultured on liquid Murashige and Skoog (1962) medium supplemented with various sucrose concentrations (0.25, 0.5, 0.75, 1.0 M) for 24 h or 48 h and dehydrated with the vitrification solution PVS2 (up to 4 h) at 24 °C or 0 °C prior to direct immersion in liquid nitrogen (−196 °C). A maximum of shoot regeneration from cryopreserved shoot tips was obtained with the following combinations: preculture in 0.5 M sucrose and 180 min dehydration treatment at 0 °C for cv. Pallas (60% shoot formation), or preculture in 0.75 M and 200 min dehydration at the same temperature for cv. Pink Candy (66.6% shoot formation) and cv. Wanessa (73% shoot formation).