蟛蜞菊属和孪花菊属(菊科-向日葵族)的细胞学研究

研究了菊科向日葵族鳢肠亚族蟛蜞菊属(Sphagneticola O. Hoffm.)和孪花菊属(Wollastonia DC. ex Decne.)各2种植物的染色体数目和染色体形态。蟛蜞菊[S. calendulacea (L.) Pruski]的染色体数目为2n=50, 核型公式为2n=18m+30sm+2st,南美蟛蜞菊[S. trilobata (L.) Pruski]的染色体数目为2n=56, 核型公式为2n=24m+28sm+4st, 孪花菊[W. biflora (L.) DC.]的染色体数目为2n=30,核型公式为2n=24m+4sm+2st,山孪花菊[W. montana (Blume) DC.]的染色体数目为2n=74, 核型公式为2n=37m+31sm+6st。根据上述结果并结合以前的有关资料,推测蟛蜞菊属的染色体基数可能为x=14和x=25,而不应是x=15。该属的3个新世界热带种[S. brachycarpa (Baker) Pruski、S. gracilis (Richard) Pruski和南美蟛蜞菊]可能都基于x=14, 其中S. gracilis为二倍体(2n=2x=28), S. brachycarpa和南美蟛蜞菊为四倍体(2n=4x=56); 唯一的亚洲种(蟛蜞菊)可能是基于x=25的二倍体(2n=2x=50)。染色体资料不支持将山孪花菊(x=37)这一植物置于孪花菊属(x=15)中。     

江西虾脊兰属一新变型——异钩距虾脊兰

描述了产自江西的兰科(Orchidaceae)虾脊兰属(Calanthe R. Br.)植物一新变型——异钩距虾脊兰 (Calanthe graciliflora f. jiangxiensis B. Li, L. J. Kong et B. Y. Yang),并绘制了线条图。该新变型与原变型钩距虾脊兰(C. graciliflora Hayata)的主要区别为距末端分裂为2个不等的短尖。     

将安龙花转移至马蓝属(爵床科)的形态特征依据

比较了安龙花(Dyschoriste sinica H. S. Lo)的模式标本与距药花属(Dyschoriste Nees)和马蓝属(Strobilanthes Bl.)部分种类的花粉和花的特征后,支持将安龙花转移到马蓝属,组合为Strobilanthes sinica (H. S. Lo) Y. F. Deng。安龙花隶属于马蓝属黄猄草群,它与日本马蓝(Strobilanthes japonica (Thunb.) Miq.)近似,但区别在于它的匍匐习性,叶矩圆状椭圆形,近无柄,花单生叶腋。因此,距药花属(Dyschoriste Nees)在中国并没有分布。     

淫羊藿属植物查耳酮合成酶启动子序列的克隆及比较分析

采用TAIL-PCR技术从箭叶淫羊藿(Epimedium sagittatum)叶片中克隆得到查耳酮合成酶基因(Chalcone synthase)的启动子,命名为ECHSP, 长度为750 bp,其具有TATA BOX、CAAT BOX、MYB结合位点、MYC结合位点等元件。对箭叶淫羊藿、木鱼坪淫羊藿(E. franchetii)、粗毛淫羊藿(E. acuminatum)、直距淫羊藿(E. mikinorii)、黔岭淫羊藿(E. leptorrhizum)等5种植物的CHS启动子序列进行比较分析,结果表明,CHS启动子的核苷酸多态性丰富,表明CHS 的表达可能受到多种因素的灵活调节。ECHSP与其他植物的CHS启动子序列进行比较,其TATA box的位置可能与黄酮类化合物的积累相关。此外,进化分析表明ECHSP的核苷酸序列可应用于淫羊藿属植物的系统进化研究。     

燕麦属不同倍性种质资源抗旱性状评价及筛选

盆栽控水试验测定了燕麦属13个二倍体、7个四倍体和5个六倍体物种共106份材料的主要抗旱性状表现,用GGEbiplot软件的主成分分析法比较了各性状之间的关系及其对抗旱鉴定的贡献,综合评价燕麦属野生资源在燕麦抗旱育种中的潜能和利用价值。结果表明,干旱处理后植株的死亡率和萎蔫程度与可溶性糖含量的增加幅度呈显著正相关关系(r>0.5, P<0.05),而胁迫后植株的丙二醛(MDA)含量和植株相对电导率与抗旱能力也明显相关(r>0.5, P<0.01)。综合考虑抗旱的相关形态和生理指标,筛选到二倍体Avena atlantica、A. wiestii 和A. strigosa,四倍体种A. murphyi,以及六倍体栽培燕麦A. sativa和普通野燕麦A. fatua的部分居群具有优良的综合抗旱性。基于A. wiestii,A. strigosa和A. murphyi与栽培燕麦较近的亲缘关系,其抗旱性可通过远缘杂交的方式在普通燕麦育种中加以利用。而对于具有明显抗旱优势的野生二倍体材料A. atlantica,则可通过克隆其抗旱基因进而遗传转化的方法将其应用于栽培燕麦的抗旱性改良。同时该研究表明燕麦的抗旱性不具有种属和分布区域的特异性,因此其抗旱性并非简单的由基因或环境决定,在确定抗旱材料时需要对个体进行全面的抗旱性评价和鉴定,以期在利用抗旱材料或通过克隆抗旱基因来改善干旱地区生态环境的实践中能更准确和有效。     

陆地革菌的化学成分研究

从陆地革菌(Thelephora terrestris)子实体中分离得到9个已知化合物,经波谱学分析鉴定为:(22E,24R)-麦角甾-7,22-二烯-3β -醇 (1),(22E, 24R)-麦角甾-7, 22-二烯-3β ,5α,6β -三醇 (2),(22E,24R)-麦角甾-4,6,8(14),22-四烯-3-酮 (3),24-亚甲基羊毛甾-8-烯-3β -醇 (4),熊果酸 (5),木栓酮 (6),cerebroside B (7),(2S,3S,4R,2'R)-2-(2'-羟基二十二碳酰氨基)-十八碳烷-1,3,4-三醇 (8),(2S,3S,4R,2'R)-2-(2'-羟基二十三碳酰氨基)-十八碳烷-1,3,4-三醇 (9)。     

中国玉叶金花属一新记录种——长瓣玉叶金花

报道中国茜草科(Rubiaceae)玉叶金花属一新记录种——长瓣玉叶金花(Mussaenda longipetala H. L. Li)。该种在形态上与尾裂玉叶金花(M. caudatiloba D. Fang)和狭瓣玉叶金花(M. lancipetal X. F. Deng & D. X. Zhang)相似,但区别在于叶片长圆状卵形或椭圆状卵形,托叶早落,正常的萼裂片长6~8 mm,花冠管长约3 cm,裂片披针形,长约12 mm。目前仅知分布于越南北部的广宁省和中国的广西北部湾沿海地区。凭证标本存放于广西植物标本馆(IBK)。     

越南拟单性木兰属一新组合

粗壮光叶拟单性木兰(Magnolia nitida var. robusta)被转移到拟单性木兰属(Parakmeria),升级为种的等级。它与光叶拟单性木兰不同,特征是:长叶片,长叶柄,雌蕊短于雄蕊,花两性或雄性,被片乳白色,附属物尖 (3~3.5 mm)。     

非洲爵床科一新组合——短穗观音草

提出一新组合——短穗观音草(Peristrophe brevispicata (I. Darbysh.) Y. F. Deng et Z. P. Hao)。     

两种猎物对南方小花蝽种群增长的影响及其对二斑叶螨的控害潜能

南方小花蝽(半翅目:花蝽科)是农田害虫的重要天敌之一。在室内,分别用米蛾卵和二斑叶螨饲养南方小花蝽,采用生命表与功能反应方法,探讨了两种猎物(米蛾卵、二斑叶螨)对南方小花蝽种群增长的影响、评价了南方小花蝽应用前景。南方小花蝽取食米蛾卵的年龄特征生命表的参数如下:世代平均历期T= 24.3500d,雌性比率P_♀=0.5250,单雌平均产卵量FP_F=37.2857头,种群趋势指数(I)=9.2118,周限增长率λ＝1.0955,内禀增长率r_m＝0.0912。取食二斑叶螨的南方小花蝽能完成发育,雌雄可交配,但不能产卵。一龄若虫的存活率为81.19%,低于其它龄期的若虫存活率(89.5%以上)。从初孵若虫至成虫死亡,平均历期为19.3716d。取食米蛾卵的南方小花蝽成虫存活率为83.33%,而取食二斑叶螨的成虫存活率为59.68%;取食米蛾卵的南方小花蝽若虫平均历期(11.0633d)短于取食二斑叶螨的(13.8950d);然而取食米蛾卵的南方小花蝽成虫平均历期(9.9750d)明显长于取食二斑叶螨的(5.7297d)。表明米蛾卵能够满足南方小花蝽生长发育的营养需求,可以用来室内饲养南方小花蝽,二斑叶螨室内不能单独用于饲养南方小花蝽。南方小花蝽成虫对二斑叶螨成螨捕食功能反应符合HollingⅡ模型,且处置时间Th=0.0108,瞬间攻击率a=0.8253,日最大捕食量Na_max =92.59 d^-1。南方小花蝽是二斑叶螨潜在的生物防治资材。     

Phylogeny of Phaeomollisia piceae gen. sp. nov.: a dark, septate, conifer-needle endophyte and its relationships to Phialocephala and Acephala

Dark, septate endophytes (DSE) were isolated from roots and needles of dwarf Picea abies and from roots of Vaccinium spp. growing on a permafrost site in the Jura Mountains in Switzerland. Two of the isolates sporulated after incubation for more than one year at 4 °C. One of them was a hitherto undescribed helotialean ascomycete Phaeomollisia piceae gen. sp. nov., the other was a new species of Phialocephala, P. glacialis sp. nov. Both species are closely related to DSE of the Phialocephala fortinii s. lat.-Acephala applanata species complex (PAC) as revealed by phylogenetic analyses of the ITS and 18S rDNA regions. Morphologically dissimilar fungi, such as Vibrissea and Loramyces species, are phylogenetically also closely linked to the new species and the PAC. Cadophora lagerbergii and C. (Phialophora) botulispora are moved to Phialocephala because Phialocephala dimorphospora and P. repens are the closest relatives. Several Mollisia species were closely related to the new species and the PAC according to ITS sequence comparisons. One DSE from needles of Abies alba and one from shoots of Castanea sativa formed Cystodendron anamorphs in culture. Their identical 18S sequences and almost identical ITS sequences indicated Mollisia species as closest relatives, suggesting that Mollisia species are highly euryoecious.     

Three new species and two new combinations in the Aizoaceae from the Western and Northern Cape of South Africa

Three new species of Aizoaceae from the Western Cape are described. Octopoma tanquanum Klak and Vlokia montana Klak are dwarf shrubby or mat-forming succulents which belong to the Ruschieae in the Ruschioideae. Mesembryanthemum knolfonteinense Klak of the Mesembryanthemoideae is a geophyte. Octopoma tanquanum inhabits relatively low lying arid areas within the Tanqua Karoo and the Little Karoo and is thought to be closely allied to the two species of Octopoma found in the Little Karoo. Both V. montana and M. knolfonteinense grow at relatively high altitudes within the fynbos biome. In addition, Ruschia littlewoodii L.Bolus is transferred to Phiambolia, and two new combinations are made in Antimima for Ruschia hexamera L.Bolus and Ruschia radicans L.Bolus.     

A revision of the Chinese Trigonalyidae (Hymenoptera,Trigonalyoidea)

The Chinese fauna of the family Trigonalyidae Cresson, 1887, is revised, keyed and fully illustrated for the first time. Eight genera of this family (Bakeronymus Rohwer, 1922, Bareogonalos Schulz, 1907, Jezonogonalos Tsuneki, 1991, re-instated, Lycogaster Shuckard, 1841, Orthogonalys Schulz, 1905, Pseudogonalos Schulz, 1906, Taeniogonalos Schulz, 1906 and Teranishia Tsuneki, 1991) are recorded from China. The genus Ischnogonalos Schulz, 1907, is synonymized with Taeniogonalos Schulz, 1906. In total 40 valid species are recognized. Twenty species are new for science: Jezonogonalos elliptifera sp. n., J. jiangliae sp. n., J. luteata sp. n., J. nigrata sp. n., Lycogaster angustula sp. n., L. flavonigrata sp. n., L. nigralva sp. n., Orthogonalys cheni sp. n., O. clypeata sp. n., O. robusta sp. n., Pseudogonalos angusta sp. n., Taeniogonalos bucarinata sp. n., T. cordata sp. n., T. geminata sp. n., T. sculpturata sp. n., T. triangulata sp. n., T. tricolorisoma sp. n., T. uncifera sp. n., Teranishia crenulata sp. n. and T. glabrata sp. n. Two species are reported new for China: Orthogonalys elongata Teranishi, 1929 and Nanogonalos flavocincta Teranishi, 1929 (renamed to Taeniogonalos subtruncata nom. n.). Seven new synonyms are proposed: Poecilogonalos yuasai Teranishi, 1938, and P. maga taiwana Tsuneki, 1991, of Taeniogonalos taihorina (Bischoff, 1914); Taiwanogonalos minima Tsuneki, 1991, and T. similis Tsuneki, 1991, of Taeniogonalos alticola (Tsuneki, 1991); P. intermedia Chen, 1949, and P. unifasciata Chen, 1949, of Taeniogonalos formosana (Bischoff, 1913). Six taxa are recognised as valid species: Bakeronymus seidakka Yamane & Terayama, 1983, Jezonogonalos laeviceps (Tsuneki, 1991), J. satoi (Tsuneki, 1991), Taeniogonalos alticola (Tsuneki, 1991), T. flavoscutellata (Chen, 1949) and T. gestroi (Schulz, 1908). Five new combinations are made: Jezonogonalos laeviceps (Tsuneki, 1991), comb. n., J. satoi (Tsuneki, 1991), comb. n., Taeniogonalos flavoscutellata (Chen, 1949), comb. n., T. gestroi (Schulz, 1908), comb. n. and T. lachrymosa (Westwood, 1874), comb. n. Lectotypes are designated for Lycogaster violaceipennis Chen, 1949, Poecilogonalos flavoscutellata Chen, 1949, P. rufofasciata Chen, 1949, and P. tricolor Chen, 1949.     

Phylogeny of Celastraceae tribe Euonymeae inferred from morphological characters and nuclear and plastid genes

The phylogeny of Celastraceae tribe Euonymeae (∼230 species in eight genera in both the Old and New Worlds) was inferred using morphological characters together with plastid (matK, trnL-F) and nuclear (ITS and 26S rDNA) genes. Tribe Euonymeae has been defined as those genera of Celastraceae with generally opposite leaves, isomerous carpels, loculicidally dehiscent capsules, and arillate seeds (except Microtropis). Euonymus is the most diverse (129 species) and widely cultivated genus in the tribe. We infer that tribe Euonymeae consists of at least six separate lineages within Celastraceae and that a revised natural classification of the family is needed. Microtropis and Quetzalia are inferred to be distinct sister groups that together are sister to Zinowiewia. The endangered Monimopetalum chinense is an isolated and early derived lineage of Celastraceae that represents an important component of phylogenetic diversity within the family. Hedraianthera is sister to Brassiantha, and we describe a second species (Brassiantha hedraiantheroides A.J. Ford) that represents the first reported occurrence of this genus in Australia. Euonymus globularis, from eastern Australia, is sister to Menepetalum, which is endemic to New Caledonia, and we erect a new genus (Dinghoua R.H. Archer) for it. The Madagascan species of Euonymus are sister to Pleurostylia and recognized as a distinct genus (Astrocassine ined.). Glyptopetalum, Torralbasia, and Xylonymus are all closely related to Euonymus sensu stricto and are questionably distinct from it. Current intrageneric classifications of Euonymus are not completely natural and require revision.     

Prepatterning the Drosophila notum: the three genes of the iroquois complex play intrinsically distinct roles

The Drosophila thorax exhibits 11 pairs of large sensory organs (macrochaetes) identified by their unique position. Remarkably precise, this pattern provides an excellent model system to study the genetic basis of pattern formation. In imaginal wing discs, the achaete-scute proneural genes are expressed in clusters of cells that prefigure the positions of each macrochaete. The activities of prepatterning genes provide positional cues controlling this expression pattern. The three homeobox genes clustered in the iroquois complex (araucan, caupolican and mirror) are such prepattern genes. mirror is generally characterized as performing functions predominantly different from the other iroquois genes. Conversely, araucan and caupolican are described in previous studies as performing redundant functions in most if not all processes in which they are involved. We have addressed the question of the specific role of each iroquois gene in the prepattern of the notum and we clearly demonstrate that they are intrinsically different in their contribution to this process: caupolican and mirror, but not araucan, are required for the neural patterning of the lateral notum. However, when caupolican and/or mirror expression is reduced, araucan loss of function has an effect on thoracic bristles development. Moreover, the overexpression of araucan is able to rescue caupolican loss of function. We conclude that, although retaining some common functionalities, the Drosophila iroquois genes are in the process of diversification. In addition, caupolican and mirror are required for stripe expression and, therefore, to specify the muscular attachment sites prepattern. Thus, caupolican and mirror may act as common prepattern genes for all structures in the lateral notum.     

Phylogenetic relationships among Southeast Asian climbing bamboos (Poaceae: Bambusoideae) and the Bambusa complex

A phylogenetic analysis of Bambusa and allies based on the plastid DNA non-coding regions rps16-trnQ, trnC-rpoB, trnH-psbA and trnD-T, and a partial nuclear GBSSI gene, was carried out. This included representatives from all four Bambusa subgenera (including type species), a group of segregate Southeast Asian genera distinctive by their climbing–scrambling culms (Dinochloa, Holttumochloa, Kinabaluchloa, Maclurochloa, Soejatmia, Sphaerobambos), and two other Bambusinae genera (Dendrocalamus, Gigantochloa). The results do not support the present subgeneric classification of Bambusa. The climbing Southeast Asian genera, all of which include species previously placed in Bambusa, are distinct from the “core Bambusa group” (type species and alliance) and the Bambusa complex generally.     

On the identity of Liolaemus nigromaculatus Wiegmann,?1834 (Iguania,Liolaemidae) and?correction?of its type locality

In the current study, we review the taxonomic status of Liolaemus nigromaculatus. Despite being the nominal species of the nigromaculatus group and being the second species of the genus Liolaemus that was described, this species is of uncertain type locality and its true identification is a matter of discussion. After carefully analyzing several digital pictures of the holotype (juvenile male), reviewing all of the literature concerning the issue, examining specimens of nearly all recognized species of the nigromaculatus group, and determining the locations visited by the specimen collector, we are able to point out the following: 1) Liolaemus nigromaculatus was collected between Puerto Viejo and Copiapó of the Atacama region in Chile, and not in Huasco 2) Liolaemus bisignatus is a nomen nudum, and populations attributed to Liolaemus bisignatus should be referred to as Liolaemus nigromaculatus. 3) There is agreement that Liolaemus copiapoensis is indistinguishable from populations currently referred to as Liolaemus bisignatus (= Liolaemus nigromaculatus), 4) Populations found in Huasco (currently considered the type locality of Liolaemus nigromaculatus) are very similar to those found in Caldera (currently considered Liolaemus bisignatus) and should be designated as Liolaemus nigromaculatus, and 5) Liolaemus oxycephalus and Liolaemus inconspicuus are not synonymous with Liolaemus nigromaculatus, although their true identities are difficult to determine. We also detail several characteristic based on the holotype of Liolaemus nigromaculatus, in addition to drawing diagnostic comparisons between this species and others belonging to the nigromaculatus group.     

The ant genus Carebara Westwood (Hymenoptera,Formicidae): synonymisation of Pheidologeton Mayr under Carebara,establishment and revision of the C. polita species group

In this paper the genus Pheidologeton Mayr, 1862 is synonymized under Carebara Westwood, 1840 and the Carebara polita group is established and revised. This species group currently includes six species from the Afrotropical region (C. madibai, C. nicotianae, C. perpusilla, C. polita, C. silvestrii, and C. villiersi) and two species from the Neotropical region (C. brevipilosa and C. urichi). The polita group clearly links Carebara and Pheidologeton, and, due to a lack of autapomorphic characters for the latter, a separation of the two genera is no longer justified. As a result Carebara is presented as a monophyletic and better defined genus that can be separated from other genera with more confidence. We present an overview of the distribution and biology of Carebara as well as images from the various genera currently in synonymy under Carebara, and discuss the characters they share. The polymorphism present in Afrotropical and Malagasy Carebara is discussed and one new species from Africa, C. madibai sp. n., is described. The subspecies Carebara perpusilla arnoldiana syn. n., Carebara perpusilla concedens syn. n., and Carebara perpusilla spinosa syn. n. are new synonyms of Carebara perpusilla. Oligomyrmex politus nicotianae is re-elevated to species level and transferred into Carebara, C. nicotianae comb. n., stat. rev.; C. punctata is a new synonym of C. silvestrii comb. n. and C. pygmaea albipes comb. n., syn n., C. pygmaea bugnioni comb. n., syn. n., and C. simularensis syn. n. are new synonyms of C. pygmaea comb. n.. The following names are transferred from Pheidologeton to Carebara as new combinations (with the species epithets adjusted to female endings where necessary): aberrans, affinis, affinis javana, affinis minor, affinis spinosior, affinis sumatrensis, ceylonensis, dentiviris, diversa, diversa draco, diversa ficta, diversa laotina, diversa macgregori, diversa philippina, diversa standfussi, diversa taprobanae, diversa tenuirugosa, diversa williamsi, hammoniae, hostilis, kunensis, latinoda, maccus, mayri, melanocephala, melasolena, nana, nanningensis, obscura, petulens, pullata, pungens, pygmaea, rubra, rugiceps, rugosa, schossnicensis, silena, silvestrii, solitaria, transversalis, trechideros, varia, vespilla, volsellata, yanoi, and zengchengensis. Three new combinations are creating secondary junior homonyms and are here replaced with new names: C. mayri (Santschi, 1928) = C. gustavmayri nom. n., C. rugosa (Karavaiev, 1935) = C. rugoflabella nom. n., and C. silvestrii (Wheeler, 1929b) = C. luzonensis nom. n. Two new combinations are creating secondary junior homonyms among species already in Carebara: C. taprobanae (Forel, 1911a) = C. sinhala nom. n., and C. nana Santschi, 1919 = C. pumilia nom. n.     

Identification of nucleopolyhedrovirus that infect Nymphalid butterflies Agraulis vanillae and Dione juno

Dione juno and Agraulis vanillae are very common butterflies in natural gardens in South America, and also bred worldwide. In addition, larvae of these butterflies are considered as pests in crops of Passiflora spp. For these reasons, it is important to identify and describe pathogens of these species, both for preservation purposes and for use in pest control. Baculoviridae is a family of insect viruses that predominantly infect species of Lepidoptera and are used as bioinsecticides. Larvae of D. juno and A. vanillae exhibiting symptoms of baculovirus infection were examined for the presence of baculoviruses by PCR and transmission electron microscopy. Degenerate primers were designed and used to amplify partial sequences from the baculovirus p74, cathepsin, and chitinase genes, along with previously designed primers for amplification of lef-8, lef-9, and polh. Sequence data from these six loci, along with ultrastructural observations on occlusion bodies isolated from the larvae, confirmed that the larvae were infected with nucleopolyhedroviruses from genus Alphabaculovirus. The NPVs from the two different larval hosts appear to be variants of the same, previously undescribed baculovirus species. Phylogenetic analysis of the sequence data placed these NPVs in Alphabaculovirus group I/clade 1b.