广西十万大山(虫脩)目三新种((虫脩)目:异(虫脩)科,(虫脩)科)

报道采自广西十万大山Ｘｉｕ目３新种,即龙州蔷Ｘｉｕ Ａｓｃｅｌｅｓ ｌｏｎｇｚｈｏｕｅｎｓｉｓ Ｃｈｅｎ ｅｔ Ｈｅ,ｓｐ．ｎｏｖ．,斑角阿异Ｘｉｕ Ａｒｕａｎｏｉｄｅａ ｍａｃｕｌａｔａ Ｃｈｅｎ ｅｔ Ｈｅ,ｓｐ．ｎｏｖ。,和刺角短肛Ｘｉｕ Ｂａｃｕｌｕｍ ｓｐｉｎｉｃｏｒｎｕｍ Ｃｈｅｎ ｅｔ Ｈｅ,ｓｐ．ｎｏｖ．,与近似种作了比较,并附主要特征图。     

西藏,云南Xiu目昆虫二新种记述（Xiu目：Xiu科）

记述Ｘｉｕ科２新种－－聂拉木短肛螨Ｂａｃｕｌｕｍ ｎｙａｌａｍｅｎｓｅ,ｓｐ．ｎ．和版纳仿短腊ＸｉｕＰａｒａｃｌｉｔｕｍｕｎｓ ｂａｎｎａｅｎｓｉｓ,ｓｐ．ｎ．。模式标本保存于中国科学院动物研究所。     

四川短肛Xiu属两新种

本文记述采自四川省Ｘｉｕ科、短肛Ｘｉｕ属Ｂａｃｕｌｕｍ Ｓａｕｓｓｕｒｅ二新种。模式标本分别存放于中国院动物研究所和北京林业大学。文中度量单位为ｍｍ。     

中国Xiu目昆虫二新纪录属与二新种记述（Xiu目：Xiu科，异Xiu科）

本文报道中国Xiu目昆虫Xiu科Phasmatidae与异Xiu科Heteronemiidae各1新纪录属：叶尾Xiu属Acr o-phylla Gray和副厚Xiu属Parapachymorpha Brunner;及其各1新种：四川叶尾XiuAcrophylla sichuanensis,sp.nov.和四副厚XiuParapachymorpha tetracantha,sp.nov.模式标本保存于西北农业大学昆虫标本馆。     

云南,广西竹节虫目二新种记述（竹节虫目：Xiu科,枝Xiu科）

本文报道采自云南大理和广西龙州的竹节虫目Ｘｉｕ科和枝Ｘｉｕ科各一新种。即滇喙尾Ｘｉｕ Ｒｈａｍｐｈｏｐｈａｓｍａ ｄｉａｎｉｃｕｎ ｓｐ．ｎｏｖ．和邻皮ＸｉｕＰｈｒａｏｒｉｅｓ ｓｉｎｉｌｉｓ ｓｐ．ｎｏｖ．。模式标本保存于北京林业大学林业资源学院,文中采用长度单位为ｍｍ。     

云南省Xiu目一新属新种（Xiu目：异Xiu科）

本文记述了异Ｘｉｕ科一新属,即滇Ｘｉｕ属Ｄｉａｎｐｈａｓｍａ ｇｅｎ。ｎｏｖ。一新种即微翅滇ＸｉｕＤｉａｎｐｈａｓｍａ ｍｉｃｒｏｐｔｅｒａ ｓｐ．ｎｏｖ。标本采自云南省小中甸,保存在中国科学院动物研究所。     

Genetic Diversity of the Wild Banana Musa acuminata Colla in Malaysia as Evidenced by AFLP

Musa acuminata Colla (Musaceae), the wild progenitor of thecultivated banana, is highly variable in Malaysia and presentsseveral unresolved nomenclatural problems. AFLP was employedto distinguish among three subspecies of Musa acuminata(subsp.truncata and subsp. malaccensis from peninsular Malaysia andsubsp. microcarpa from Borneo) and to examine whether subsp.truncata is a distinct taxon. Eight primer combinations revealedmolecular markers specific for each of the three taxa. UPGMAcluster analysis showed the three taxa were distinct. Subspeciesmalaccensis which is endemic in peninsular Malaysia and subsp.microcarpa which is endemic in Borneo were found to be moresimilar to each other in their DNA patterns than they are tosubsp. truncata, which is endemic to peninsular Malaysia. Sincesubsp. truncata is genetically separate from subsp. malaccensisand subsp.microcarpa , it cannot be regarded as synonymous witheither of these subspecies. This paper sheds light on the nomenclatureof the three subspecies of Musa acuminata. Copyright 2001 Annalsof Botany Company Musa acuminata Colla, truncata, malaccensis, microcarpa, Musaceae, wild banana, genetic diversity, AFLP, DNA fingerprinting     

Estimating the capacity for improvement in risk prediction with a marker

Consider a set of baseline predictors X to predict a binaryoutcome D and let Y be a novel marker or predictor. This paperis concerned with evaluating the performance of the augmentedrisk model P(D = 1|Y,X) compared with the baseline model P(D= 1|X). The diagnostic likelihood ratio, DLR_X(y), quantifiesthe change in risk obtained with knowledge of Y = y for a subjectwith baseline risk factors X. The notion is commonly used inclinical medicine to quantify the increment in risk predictiondue to Y. It is contrasted here with the notion of covariate-adjustedeffect of Y in the augmented risk model. We also propose methodsfor making inference about DLR_X(y). Case–control studydesigns are accommodated. The methods provide a mechanism toinvestigate if the predictive information in Y varies with baselinecovariates. In addition, we show that when combined with a baselinerisk model and information about the population distributionof Y given X, covariate-specific predictiveness curves can beestimated. These curves are useful to an individual in decidingif ascertainment of Y is likely to be informative or not forhim. We illustrate with data from 2 studies: one is a studyof the performance of hearing screening tests for infants, andthe other concerns the value of serum creatinine in diagnosingrenal artery stenosis.     

The GUS reporter-aided analysis of the promoter activities of Arabidopsis ACC synthase genes AtACS4, AtACS5, and AtACS7 induced by hormones and stresses

Ethylene biosynthesis in higher plants is regulated developmentallyand environmentally. To investigate the regulation of ACC synthasegene expression, the promoters of Arabidopsis ACS genes, AtACS4,AtACS5, and AtACS7, were fused to a GUS reporter gene, and therecombinant transgenes were introduced into Arabidopsis to producethree groups of AtACS::GUS transgenic plants. Histochemic andfluorometric study of these transgenic plants revealed thatpromoters of AtACS4, AtACS, and AtACS7 are all active in dark-germinatedseedlings. AtACS5 has the highest promoter activity in leavesof 2-week-old light-grown seedlings among the three AtACS genesstudied. In the mature leaves, AtACS4 and AtACS7 genes are expressedin both veins and areoles, whereas AtACS5 is expressed at ahigher level in the areoles and epidermal cells surroundingtrichomes. The promoter activities of all these AtACS genesare found in the reproductive organs. AtACS5 and AtACS7 arehighly expressed in petals, sepals, carpels, stamens, caulineleaves, inflorescence stems, and siliques, while AtACS4 expressionis undetectable in the petals of open flowers. All three AtACSgenes are expressed in root tissue. In the 2-week-old light-grownArabidopsis, the AtACS4 promoter is responsive to the planthormones IAA, ethylene, and ABA, and to darkness and wounding;the AtACS5 promoter to IAA, ABA, salt, high temperature, andwounding; and the AtACS7 promoter to GA₃, ethylene, and ABA,and to darkness and salt. Low-temperature treatment abolishesthe darkness-induced AtACS7 gene expression, but not that ofAtACS4. Each AtACS gene has a unique expression profile duringgrowth and development. It appears that at any developmentalstage or any growth period of Arabidopsis, there is always amember of AtACS multigene family that is actively expressed. Key words: ACC synthase, Arabidopsis, ethylene, gene expression, GUS histochemical staining, reporter, stress treatments     

Leaf Survival and Evolution in Betulaceae

Studies on the changes in leaf number of 12 species of Betulaceaewere carried out by repeated observations during several years.The inner structure of the winter buds of these species wasalso examined. The periods of leaf emergence were long in Alnusand Betula, intermediate in Corylus and short in Ostrya andCarpinus. A heavy summer leaf fall is characteristic only ofthe Gymnothyrsus subgenus of Alnus. One lamina and two stipulesis the basic unit constituting the winter buds. Only the budsof Gymnothyrsus are composed of several of these units. In theAlnaster subgenus of Alnus, Betula and Corylus, there are oneor two scales that seem to have originated from the two stipulesremaining after reduction of the lamina. Eight and 24 scalesof similar origin were found in Ostrya and Carpinus respectively.A common ancestral species having the following primitive charactersis proposed: shoot constituted only of the equal-sized units,period of leaf emergence long, and leaf fall usually occurs.Alnus (Gymnothyrsus) is assumed to be the most primitive typeas it has many characters similar to those of the proposed ancestralspecies. Carpinus is assumed to be the most advanced group.The leaf survivorship curve is assumed to have changed fromthe primitive bell-shaped to an advanced trapezoid concurrentwith an increase in the number of bud scales. Betulaceae, Alnus, Betula, Carpinus, Corylus, Ostrya, leaf survival, leaf emergence, stipules, winter buds, evolution     

Structure of the dnaA region of the endosymbiont, Buchnera aphidicola, of aphid Schizaphis graminum

Buchnera aphidicola is an intracellular prokaryote (endosymbiont)that lives in the body cavity of the aphid. Phylogenetic studiesindicated that it is closely related to Escherichia coli andmembers of Enterobacteria. The gene order of the region containingthe dnaA gene is well conserved in many bacteria. Seven genesof the endosymbiont of the aphid Schizaphis graminum, gyrB,dnaN, dnaA, rpmH, rnpA, yidD, and 60K, were found to be homologousin sequence and relative location to those of E. coli. We havefurther sequenced the region downstream of the 60K gene to elucidatethe boundary of the conserved region, and found that one moregene, thdF , is conserved. The comparison of gene organizationsof the dnaA region of the related bacteria supported the closephylogenetic relationship of B. aphidicola to E. coli. In addition,we have identified groES and groEL genesnext to the thdF gene.GroEL protein was reported to be expressed at an elevated levelin the endosymbionts of aphids, and is considered to play animportant role in their association with the aphid host. Comparisonof the structure of the groE operon with that of the endosymbiontof the aphid Acyrthosiphon pisum revealed the conservation ofa sequence resembling the E. coli consensus heat shock promoter,and this sequence may be responsible for the high expressionof the groEL gene in aphid endosymbionts.     

Leaf and Flower Development in Pea (Pisum sativum L.): Mutants cochleata andunifoliata

The stipule mutant cochleata(coch) and the simple-leaf mutantunifoliata(uni) are utilized to increase understanding of the controlof compound leaf and flower development in pea. The phenotypeof the coch mutant, which affects the basal stipules of thepea leaf, is described in detail. Mutant coch flowers have supernumeraryorgans, abnormal fusing of flower parts, mosaic organs and partialmale and female sterility. The wild-type Coch gene is shownto have a role in inflorescence development, floral organ identityand in the positioning of leaf parts. Changes in meristem sizemay be related to changes in leaf morphology. In the coch mutant,stipule primordia are small and their development is retardedin comparison with that of the first leaflet primordia. Thediameter of the shoot apical meristem of the uni mutant is approx.25% less than that of its wild-type siblings. This is the firsttime that a significant difference in apical meristem size hasbeen observed in a pea leaf mutant. Genetic controls in thebasal part of the leaf are illustrated by interactions betweencoch and other mutants. The mutantcoch gene is shown to changestipules into a more ‘compound leaf-like’ identitywhich is not affected by thestipules reduced mutation. The interactionof coch and tendril-less(tl) genes reveals that the expressionof the wild-type Tl gene is reduced at the base of the leaf,supporting the theories of gradients of gene action. Copyright2001 Annals of Botany Company Pisum sativum, garden pea, leaf morphogenesis, compound leaf, leaf mutants, flower morphology     

Some Observations on the Diversity of Stomata and Trichomes in Six Species of Dioscorea

Stomata and trichomes are described on the leaves of six speciesof Dioscorea. As many as six types were found in D. bulbiferaand D. oppositifolia, four types in D.hispida and D. wallichii,three types in D. belophylla, but only two types in D. alata.Although there is a diversity of stomata even on the same surface,the predominant type is anomocytic in all the species exceptD. bulbifera in which it is tricytic. Rarely a stoma is alsocyclocytic in D. bulbifera. An increase in the number of subsidiarycells in paracytic, tricytic, or diacytic stomata takes placeby the wall formation in them. Similarly a reduction in thenumber of subsidiary cells of a tetracytic stoma is the resultof lateral subsidiary cells assuming the form of epidermal cells.Abnormalities such as a stoma with one guard cell, degenerationof guard cells, and contiguous stomata are also met with. Theorganization of different types of stomata is studied in D.bulbifera and D. wallichii and shown to be perigenous. Capitateglandular hairs were seen on the leaves of D. belophylla, D.bulbifera, D. hispida, and D. wallichii but non-glandular, uniseriate,3-celled trichomes were observed only in D. hispida.     

Intergeneric and Interspecific Relationships in Araceae tribe Caladieae and Development of Molecular Markers using Amplified Fragment Length Polymorphism (AFLP)

Since amplified fragment length polymorphism (AFLP) analysishas proved useful in distinguishing cultivars of Caladium, itwas used to assess the status of species of Caladium vs. Xanthosoma,both in tribe the Caladieae, and to reassess the position ofHapaline in the same tribe. AFLP analysis using three primercombinations was carried out on four species of Caladium(C.bicolor, C. humboldtii, C. lindenii and C. schomburgkii). Resultsshowed that AFLP can distinguish between the different speciesby their unique and different banding patterns. AFLP analysisconfirmed that C. humboldtii is a species distinct from C. bicolorand that C. lindenii is a true Caladium species and does notbelong to Xanthosoma. UPGMA cluster analysis showed that C.bicolor and C. schomburgkii are most similar and that C. humboldtiiis closer to the C. bicolor / C. schomburgkii cluster comparedwith C. lindenii. Genetic relationships between Caladium, Xanthosoma,Hapaline, Alocasia and Protarum were also examined by AFLP analysisusing eight primer combinations. Several useful molecular markerswere specific either to Caladium orXanthosoma , so that AFLPcan be used to distinguish species of these two genera. Geneticanalysis of the genera examined confirms that the Caladieaeand Colocasieae tribes are distinct and that Hapaline fallswithin the tribe Caladieae and that Protarum is most distantfrom all the genera examined. Copyright 2000 Annals of BotanyCompany Araceae, Caladium, Xanthosoma, Hapaline, Alocasia, Protarum, AFLP DNA fingerprinting, diversity, AFLP markers