西藏地区拟康蝗属一新种(直翅目：网翅蝗科）

记述采自中国西藏网翅蝗科拟康蝗属Kangacrisoides Wang et al.,2006 1新种：江达拟康蝗Kangacrisoides jiangdaensis sp. nov.。新种同霍城拟康蝗K. huochengensis Wang, Zheng & Niu, 2006近似,其区别特征为：头背面具中隆线;雄性头侧窝长为宽的2.5–3倍,而雌性为3倍;雌性前翅在背面狭分开,而雄性刚刚相连;雄性前翅顶到达第5–6腹节背板,而雌性到达第4腹节背板;雄性中脉域为肘脉域宽2倍,而雌性为3倍;后足胫节内侧之上、下距近等长;鼓膜孔宽卵形;雌性下生殖板后缘角形突出。     

新疆网翅蝗科一新属一新种(直翅目,蝗总科)

记述采自新疆网翅蝗科1新属1新种,即拟康蝗属Kangacrisoides gen．nov．、霍城拟康蝗Kangacrisoides huochengensis sp．nov．,新属近似于康蝗属Kangacris Yin,1983,主要区别为：头侧窝长宽之比矛2．4-2．5,♀2．0;前翅叶片状,侧置,在背部较狭地分开;鼓膜器狭缝状;雄性阳茎基背片桥拱较平直,侧板外缘平直。模式标本保存于陕西师范大学动物研究所标本室。     

中国窝蝗属一新种：直翅目：蝗总科：剑角蝗科

本文了剑角蝗科窝蝗属１新种：郑氏窝蝗Ｆｏｖｅｏｌａｔａｃｒｉｓ ｚｈｅｎｇｉ,ｓｐ．ｎｏｖ。,采自甘肃省南县宝瓶河牧场;并据此对属征作了必要的修订,给出了分种检索表。模式标本保存于陕西师范大学动物研究所。     

甘肃省雏蝗属一新种记述（蝗总科：网翅蝗科）

本文记述了雏蝗属一新种：短角雏蝗（Ｃｈｏｒｔｈｉｐｐｕｓｂｒｅｖｉｃｏｒｎｉｓｓｐ．ｎｏｖ．,采自甘肃省肃南县宝瓶河牧场。模式标本存于陕西师范大学动物研究所。     

中国台湾佛蝗属一新种(直翅目,剑角蝗科,佛蝗亚科)

记述了采自中国台湾剑角蝗科佛蝗亚科佛蝗属Phlaeoba Stal,1860的1新种南投佛蝗Phlaeoba nantouensis sp.nov.,该新种近似台湾佛蝗Phlaeoba formosana（Shiraki,1910）,区别特征为前翅较长,超过第3腹节背板的后缘;触角中段一节的长为宽的4倍;肛上板中纵沟深,两侧平行。模式标本保存于国立自然科学博物馆,台中。     

斑腿蝗科五种蝗卵的形态记述

本文记述了在云南西双版纳和陕西省秦岭地区收集到的斑腿蝗科５种蝗卵的形态。     

云南蝗属一新种及中甸拟澜沧蝗雌性记述(直翅目,瘤锥蝗科)

记述采自滇西北横断山地区云南蝗属1新种,即郑氏云南蝗Yuannanites zhengi sp．nov．,模式标本保存于云南大理学院生命科学与化学系;编写了该属的分种检索表。另记述中甸拟澜沧蝗的雌性。     

黑龙江省金色蝗属一新种 (直翅目：蝗总科)

 报道了采自黑龙江省的蝗总科昆虫一新种：佳木斯金色蝗Chry sacris jiamusi sp.nov.,并与其近似种辽宁金色蝗Ch.liaoningensis Zheng和秦岭 金色蝗Ch.qinlingensis Zheng做了比较。模式标本保存于东北师范大学生命科学学院 动物标本室。     

贺兰山地区雏蝗属二新种记述(直翅目:网翅蝗科)

记述在贺兰山西侧阿拉善左旗采到的网支蝗科雏蝗二新种，即阿拉善雏蝗Ｃｈｏｒｔｈｉｐｐｕｓ ａｌｘａｅｎｓｉｓ Ｚｈｅｎｇ，ｓｐ．ｎｏｖ，及哈拉乌雏蝗Ｃｈｏｒｔｈｉｐｐｕｓ ｈａｌａｗｕｅｎｓｉｓ Ｚｈｅｎｇ，ｓｐ，ｎｏｖ．。     

新疆网翅蝗科一新属一新种（直翅目：蝗总科）

本文记述了采自中国新疆的网翅蝗科１新属：短翅蝗属及１新种：尼勒克短翅蝗。模式标本存于陕西师范大学动物研究所蝗虫标本室。     

MORE MOLLUSCAN NAME-CHANGES, GENERIC AND SPECIFIC

Volema, Bolten, type V. paradisiaca, Bolten, has priority overMelongena, Schumacher, but may be used independently. Mayena, gen. nov., proposed for Biplex australasia, Perry. Turricula, Schumacher, is the correct name for Surcula, H. &A. Adams. Gelagna, Schaufuss, is equal to and antedates Paralagena, Dall. Partulida, Schaufuss, should replace Spiralinella, Chaster. Campanile, Fischer, has for type the recent species Cerithiumleve, Quoy & Gaimard, which is here renamed Campanile symbolicum,sp. nov. Campanilopa, gen. nov., introduced for the fossil Cerithiumgiganteum. Lam. Pleurotomoides, Bronn, has priority over Lora, Gistel, and Clathurella,Carpenter, all proposed as alternatives for Defrancia, Millet,preoccupied. Gabrielona, gen. nov., proposed for Phasianella nepeanensis,Gatliff & Gabriel. Orbitestella, gen. nov., for Cyclostrema bastowi, Gatliff. Megathura, Pilsbry, should be used instead of Macrochasma, Dall. Mitromorpha, auctt., is not Mitromorpha, Carpenter, which wasbased on Daphnella (?) filosa, Carpenter. Antimitra, gen. nov., is proposed for Pleurotoma agrota, Reeve,with which A. Adams' Mitromorpha lirata is congeneric. Lovellona, gen. nov., type Conus atramentosus. Reeve. Apaturris, gen. nov., type Mitramorpha expeditionis, Oliver. Callanaitis, gen. nov., type Venus yatei, Gray, for Salacia,Jukes-Browne, preoccupied. Anopsia, Gistel, is available for Psyche, Rang, preoccupied,and has priority over Verrillopsyche, Cossmann, proposed forHalopsyche, Kieferstein, preoccupied, introduced as substitutefor Rang's name. Hydromyles, Gistel, should be used for Euribia, Rang, preoccupied,as it is older than Kieferstein's name Theceurybia, for thesame genus. (Received 13 April 1917;     

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.     

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.     

FLC or not FLC: the other side of vernalization

Vernalization is the promotion of the competence for floweringby long periods of low temperatures such as those typicallyexperienced during winters. In Arabidopsis, the vernalizationresponse is, to a large extent, mediated by the repression ofthe floral repressor FLC, and the stable epigenetic silencingof FLC after cold treatments is essential for vernalization.In addition to FLC, other vernalization targets exist in Arabidopsis.In grasses, vernalization seems to be entirely independent ofFLC. Here, the current understanding of FLC-independent branchesof the vernalization pathway in Arabidopsis and vernalizationwithout FLC in grasses is discussed. This review focuses onthe role of AGL19, AGL24, and the MAF genes in Arabidopsis.Interestingly, vernalization acts through related molecularmachineries on distinct targets. In particular, protein complexessimilar to Drosophila Polycomb Repressive Complex 2 play a prominentrole in establishing an epigenetic cellular memory for cold-regulatedexpression states of AGL19 and FLC. Finally, the similar networktopology of the apparently independently evolved vernalizationpathways of grasses and Arabidopsis is discussed. Key words: AGL19, Arabidopsis, chromatin, epigenetics, FLC, flowering time, polycomb, PRC2, vernalization Received 19 December 2007; Revised 11 February 2008 Accepted 15 February 2008     

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     

NOTES ON THE TAXONOMY, SPAWN AND LARVAL DEVELOPMENT OF SOUTH AFRICAN SPECIES OF THE INTERTIDAL LIMPET SIPHONARIA (GASTROPODA: PULMONATA)

The taxonomy of South African Siphonaria is reviewed. We concludethat nine species are valid. These are: S. anneae Tomlin, 1944;S. capensis Quoy & Gaimard, 1833; S. compressa Allanson,1959; S. concinna Sowerby, 1824; S. dayi Allanson, 1959; S.nigerrima Smith, 1903; S. oculus Krauss, 1848; S. serrata (Fischer,1807) and S. tenuicostulata Smith, 1903. Of these, Siphonarianigerrima Smith, 1903, has been incorrectly synonymized withSiphonaria carbo Hanley, 1858, which is not present on SouthAfrican shores. S. aspera Krauss, 1848 is reduced to a juniorsynonym of S. Serrata (Fischer, 1807). Shell characteristicsand mode of larval development are described for these nineSouth African species. All species deposit benthic egg massesand development may be either planktonic with swimming veligerlarvae (S. capensis, S. concinna and S. oculus) or direct, withcrawling larvae emerging from the eggs (S. anneae, S. compressa,S. dayi, S. nigerrima, S. serrata and S. tenuicostulata). (Received 20 November 1992; accepted 24 January 1994)     

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