河南兜姬蜂属一新种(膜翅目:姬蜂科)

报道采自河南的兜姬蜂属Dolichomitus Smith 1新种：济源兜姬蜂Dolichomitus jiyuanensis Lin,sp．nov．。模式标本保存在国家林业局森林病虫害防治总站。     

中国臭蚁属一新种记述(膜翅目:蚁科)

记述了采自中国湖北省恩施市大吉镇的臭蚁属Dolichoderus Lund 1新种：大吉臭蚁D．dajiensis,sp．nov．。模式标本保存在陕西师范大学动物研究所标本室。     

云南丝尾螋属一新种(革翅目:丝尾螋科)

记述采自云南省丝尾螋属l新种：六库丝尾螋Diplatys liukuensis,sp．nov．。模式标本保存于浙江自然博物馆。     

复合酶解法提取三七皂苷的实验研究

以三七提取液中总皂苷的含量和提取物得率为指标,考察了乙醇回流法、渗漉法、纤维素酶解法、果胶酶解法、复合酶解法的优劣,并采用单因素法和四因素（纤维素酶用量、果胶酶用量、酶解温度、乙醇浓度）三水平正交设计法对复合酶解法提取工艺条件进行优选,得到如下较理想的提取工艺条件：纤维素酶用量为15U／g（生药）、果胶酶用量为140U／g（生药）,酶解pH值为4．5,酶解温度为50℃,乙醇浓度为80％,提取时间为2．5h。所得三七提取液中总皂苷的含量为12．01％,提取物得率为35．82％。     

杜鹃花科白珠树属分子系统学和生物地理学研究进展

白珠树属(Gaultheria) 在杜鹃花科(Ericaceae)系统演化中占有十分重要的地位, 其系统位置和演化关系一直备受争议。最近的分子系统学研究认为, 白珠树属已经不再属于传统上的越橘亚科(Vaccinioideae)的綟木族(Andromedeae), 而是与一些相关属组成了白珠树族(Gaultherieae)。对白珠树属产于美洲的类群和相关类群的分子系统学的初步研究则表明, 该属与Diplycosia、Tepuia和Pernettya等属(均为“常绿类群”)关系密切, 可能应将这几个属并入到白珠树属中, 但其属下分类系统关系还需要对产于亚洲的类群进行深入的研究后才能确定。白珠树属与其近缘属的进化历史和生物地理学关系较为复杂, 与杜鹃花科其他大多数属不同, 白珠树属为典型的环太平洋分布。关于白珠树属的起源问题存在两种不同的推测: 一种观点认为该属起源于南半球的冈瓦纳古陆; 另一种观点则认为其起源于北半球的劳亚古大陆。本文概述了近年来白珠树属的分子系统学和生物地理学研究进展, 并对该属尚存的一些问题进行了讨论。     

斑龙芋属(天南星科) 及近缘属植物的叶表皮形态

光镜、电镜下观察了天南星科天南星族下斑龙芋属2 个种及近缘属13 个种植物的叶表皮形态特征。实验结果显示, 4 属植物的叶表皮组成及其形态特征较相似, 属间不存在明显差异, 但某些特征在种间存在差异, 可作为种的鉴别特征。叶表皮特征支持将单籽犁头尖和昆明犁头尖两个种合并为一个种。15 个种的气孔器均具有2 个副卫细胞, Stebbins and Khush 认为这是气孔器类型中较具2 个以上副卫细胞更进化的一种类型, 而天南星科大多数族的气孔器都具有2 个以上的副卫细胞, 这也证明了天南星族是天南星科较进化的族。     

纯氧对采后杨梅果实腐烂的抑制与抗病相关酶的诱导

为研究高氧对抑制果实腐烂的作用及其与抗病相关酶活性诱导的关系,将杨梅果实采后在5℃用纯氧或空气(对照)处理12 d.结果表明,纯氧处理可显著抑制果实腐烂发生,贮藏12 d后对照果实的腐烂指数达到54%,而处理果实仅为17%.纯氧处理在贮藏前期可诱导杨梅果实几丁质酶和β-1,3-葡聚糖酶活性的升高,并在第6天时达到高峰.另外,纯氧处理增加了苯丙氨酸解氨酶和过氧化物酶的活性及总酚含量,并在整个贮藏期间一直高于对照水平.这些结果表明,高氧抑制杨梅果实腐烂的作用与诱导与抗病相关的酶的活性升高密切相关,抗病性诱导是高氧抑制杨梅果实腐烂的重要原因.     

Loss of Genetic Diversity of Domesticated Panax notoginseng F H Chen as Evidenced by ITS Sequence and AFLP Polymorphism： A Comparative Study with P. stipuleanatus H T Tsai et K M Feng

In the present study, we evaluated the genetic diversity of Panax notoginseng F H Chen, a domesticated species, and P. stipuleanatus H T Tsai et K M Feng, an endangered wild species in southeastern Yunnan and adjacent areas in Vietnam, using sequences of the internal transcribed spacer (ITS) regions of nuclear ribosomal DNA and amplified fragment length polymorphism (AFLP) markers. Twenty-four accessions from three plantations of P. notoginseng and 51 samples from eight populations of P. stipuleanatus were assayed. A total of 694 bp of partial sequences of 18S, ITS 1, 5.8S, ITS2, and partial sequences of 26S were obtained. No sequence variation was detected within P. notoginseng and nine sites (1.30%) were variable in P. stipuleanatus. Two-thirds of the variable sites were found between Langqiao and other populations. In P. notoginseng, four pairs of AFLP primer combinations generated 312 bands, of which 240 (76.9%) were polymorphic and 60.15% of the polymorphisms were harbored within plantations. Approximately 41.0% and 66.9% of bands were polymorphic in population D7 and 5589, respectively. In P.stipuleanatus, the same four primer combinations produced 346 bands, of which 334 (96.5%) were polymorphic and approximately 62.14% of polymorphisms were maintained within populations. Considerable variations were observed. The percentage of polymorphic bands ranged from 50.2% to 84.9% and the average over populations was 70.9%. Cluster analysis did not show correlation of genetic differentiation with the distinctive leaf morphology of P. stipuleanatus (i.e. one form with bipinnatifid leaflets and the other with undivided leaflets). Because over 40% of genetic variations were maintained among populations and because of the very restricted distribution of P. stipuleanatus, all natural populations of this species should be conserved in situ. Considering that there are variations in P. notoginseng within and among plantations, we suggest establishing a genetic resource conservation garden or reintroducing P. notoginseng into its native habitats in southwestern China. Such reintroduction should be carefully executed after large-scale screening of genetic variation within the species.     

M-PCR： a powerful method for rapid molecular identification of Trichogramma wasps （Hymenoptera： Trichogrammatidae）

Two species-specific primers were designed depending on ITS2 sequence variation of 37 Trichogramma wasps, and these primers were applied to establish an assay,multiplex PCR (M-PCR), for molecular diagnosis of two important Trichogramma wasps,T. confusum and T. dendrolimi, in China. Multiplex-PCR results showed that only target species produced two PCR products, one product of ITS2 region species-specific amplification and one product of its ITS 1 region universal amplification, but other species produced only one ITS1 universal PCR product. Using this method, the target Trichogramma species can be distinguished from other Trichogramma species. Molecular identification based on M-PCR has particular value over morphological technology and other approaches, such as normal molecular and biochemical methods. Furthermore, because M-PCR assay can avoid false negative results, which frequently happen in PCR reaction, this method will be much more accurate and useful for Trichogramma identification, and can be developed as an easy and rapid diagnostic kit applied in the identification and quality monitoring of Trichogramma mass products both in the factory and in the field. Such an easy and rapid diagnostic kit will be valuable in the application of Trichogramma species as a biological control.     

广东鹤山、东莞莲花山小蛾类(Ⅰ)

对广东省鹤山和东莞莲花山自然保护区的小蛾类昆虫进行调查,计有8科35属43种.其中广东新记录种14种.