624. DACTYLICAPNOS VENTII

Summary Dactylicapnos ventii (Khánh) Lidén is described and illustrated. Misidentification when this species was first introduced into cultivation has led to confusion with D. lichiangensis (Fedde) Hand.‐Mazz.     

Seed-coat anatomy in Fumariaceae-Fumarioideae

Seed-coat anatomy is described in 122 species of Fumarioideae, which represent all the genera, subgenera, and most sections. Nine seed-coat types were recognized: (I) Dicentra subg. Hedycapnos , (II) Dicentra subg. Chrysocapnos , (III) Dicentra subg. Macranthos , (IV) Dicentra subg. Dicentra , (V) Corydalis p.p. , (VI) rest of Corydaleae, Cysticapnos, Pseudofumaria and Ceratocapnos , (VII) Discocapnos and Sarcocapnos p. p. , (VIII) Sarcocapnos p. p., Platycapnos and Trigonocapnos , and (IX) Fumariinae. Variable characters are polarized based on the comparison with Fumariaceae Hypecooideae, Papaveraceae and Pteridophyllaceae. It is assumed that endotestal seed-coat type (I) is most primitive, that exotestal seed coat types (II—VIII) are derived therefrom, and that the reduction of the mechanical layer, including the origin of thin seed-coat type (IX) occurred repeatedly in combination with indehiscent, hard-walled fruits. Dicentra subg. Hedycapnos (with type I) possesses a combination of primitive testal characters unique within the subfamily, suggesting it represents a sister group to the rest of the subfamily. Each of the other subgenera (with II, III or IV) is also characterized by a unique combination of seed-coat characters, which are found in the outgroups but not in the other genera. Seed-coat characters support the monophyly of Fumarioideae exclusive of Dicentra subg. Hedycapnos , Fumarioideae exclusive of Dicentra , of Dicentra subg. Dicentra , of Corydalis p.p. , and of Fumariinae.     

HYBRIDIZATION AND CYTOTAXONOMY OF DICENTRA

Biosystematic relationships among species assigned to three subgenera of the genus Dicentra were investigated with respect to hybridization and chromosomal constitution and fertility of the hybrids. Four species of subgenus Dicentra, D. formosa, D. eximia, D. nevadensis, and D. peregrina, were intercrossed in various ways to form diploid, triploid, and tetraploid hybrids. Hybrids at the tetraploid level in this subgenus invariably were highly fertile. Triploid hybrids, as expected, were mostly very sterile. Diploid hybrids varied in this respect, but none was highly fertile. Crosses with two of the remaining four species of subgenus Dicentra produced no hybrids, but abundant seed was obtained in one instance. The two species of the subgenus Chrysocapnos, D. chrysaniha and D. ochroleuca, cross to produce a partially fertile tetraploid hybrid, but cross-pollinations involving these species with those of other subgenera failed. The single species of subgenus Hedycapnos, D. spectablis (diploid) produced no hybrids when cross-pollinated with members of the other two sections. These results are fully concordant with presumed affinities based on morphological similarity In addition, preliminary results of hybridization between the monocotyledonous D. peregrina and a number of dicotyledonous species of Dicentra are reported.     

Phylogeny and classification ofFumariaceae, with emphasis onDicentra s. l., based on the plastid generps16 intron

The phylogeny ofFumariaceae, as inferred fromrps16 intron sequences, is compared with morphological data, and nrDNA-ITS. The different data sets are largely congruent and indicate that (1)Dicentra and the tribeCorydaleae as hitherto circumscribed are polyphyletic, (2)Lamprocapnos (=Dicentra spectabilis) is sister group to the rest of subfam.Fumarioideae, (3)Ehrendorferia, gen. nov. (=Dicentra chrysantha andD. ochroleuca) is basal in the latter group, (4) the morphologically aberrantIchtyoselmis, gen. nov. (=Dicentra macrantha) groups withDicentra s. str., (5) the genusCysticapnos should be included in the tribeFumarieae, (6)Dactylicapnos (=Dicentra subg.Dactylicapnos) is sister group toCorydalis, (7) the genusCorydalis is monophyletic, and consists of three subgenera:Chremnocapnos, stat. nov.,Sophorocapnos, stat. nov., andCorydalis. The following new combinations are validated:Ehrendorferia chrysantha, E. ochroleuca, Ichtyoselmis macrantha, andLamprocapnos spectabilis. Dedicated to emer. Univ.-Prof. DrFriedrich Ehrendorfer on the occasion of his 70th birthday     

浙江薹草属（莎草科）新分类群

摘要描述及图解了浙江薹草属Carex 5新种和1新变种,它们是：灰帽薹草组sect. Mitratae Kükenth.的天目山薹草Carex tianmushanica C. Z. Zheng & X. F. Jin和拟三穗薹草C. pseudotristachya X. F. Jin & C. Z. Zheng;匏囊薹草组sect. Lageniformes (Ohwi) Nelmes的密毛薹草C. densipilosa C. Z. Zheng & X. F. Jin;菱形果薹草组sect. Rhomboidales Kükenth.的浙南薹草C. austrozhejiangensis C. Z. Zheng & X. F. Jin和朝芳薹草C. chaofangii C. Z. Zheng & X. F. Jin;疏花薹草组sect. Laxiflorae Kunth的无芒长嘴薹草C. longerostrata C. A. Mey. var. exaristata X. F. Jin & C. Z. Zheng。     

中国颊脊隐翅虫属附点颊脊隐翅虫亚属三新种(鞘翅目,隐翅虫科,隐翅虫亚科)

记述中国颊脊隐翅虫属Quedius附点颊脊隐翅虫亚属Distichalius 3新种,王氏附点颊脊隐翅虫Quedius(Distichalius)wangi sp.nov.,仙附点颊脊隐翅虫Quedius(D.)xiansp.nov.,和卧龙附点颊脊隐翅虫Quedius(D.)wolong sp.nov.。俯附点颊脊隐翅虫Q.(D.)lin Smetana和日本附点颊脊隐翅虫Q.(D.)pretiosus Sharp分别在中国大陆和重庆市是首次记录。3新种都隶属克什米尔附点颊脊隐翅虫群thekashmirensis group,该群为中国新纪录群。2新纪录种,俯附点颊脊隐翅虫和日本附点颊脊隐翅虫,分别是连附点颊脊隐翅虫群theannectens group和查特附点颊脊隐翅虫群thechaterjeei group的成员。     

基于叶绿体四个DNA 片段联合分析探讨山茶属长柄山茶组、金花茶组和超长柄茶组的系统位置与亲缘关系

为探讨山茶属茶亚属 (Camellia subgenThea) 中长柄山茶组 (sectLongipedicellata)、金花茶组 (sectChrysantha)和超长柄茶组 (sectLongissima) 的系统位置和亲缘关系,本研究选取了该属4个亚属11组28个种及2个外类群的材料,对这些材料的叶绿体4个DNA片段 (rpl16、psbA trnH、trnL F和rpl32 trnL) 进行了测序,运用邻接法 (neighbor joining)、最大简约法 (maximum parsimony) 和贝叶斯推断 (Bayesian inference) 对获得的序列进行了联合矩阵分析,并构建基因树。基因树的拓扑结构显示：1) 金花茶组包括3个平行的支系,并且长柄山茶组的模式种长柄山茶 (Camellia longipedicellata) 嵌于其中一个支系,因而金花茶组可能是一个并系或多系类群;2) 长柄山茶与越南分布的金花茶组种类在分子系统树上构成一个单系支,暗示了长柄山茶组和金花茶组之间可能具有紧密的亲缘关系;3) 超长柄茶组不是一个单系类群,该组的河口超长柄茶 (C. hekouensis) 位于系统树的基部,与山茶属其余种构成姐妹群。由于缺乏更广泛取样的分析,超长柄茶在山茶属中的系统位置仍然不明确,超长柄茶组与长柄山茶组的亲缘关系问题也没有得到解决。     

Phylogeny of Camellia sects Longipedicellata,Chrysantha and Longissima (Theaceae) Based on Sequence Data of Four Chloroplast DNA Loci

We focused on the systematic positions and relationships of three sections of Camellia subgenThea of Theaceae, i.e., sect.Longipedicellata, sect.Chrysantha (golden camellias) and sect.Longissima by using four chloroplast DNA regions (rpl16, psbA trnH, trnL F & rpl32 trnL). We sampled 28 species representing four subgenus, 11 sections in Camellia and two outgroups. Combined analyses of chloroplast DNA sequence data sets are performed with the neighbor joining, maximum parsimony and Bayesian inference methods, and the gene trees are constructed. The topologies of gene trees revealed that: 1) sect. Chrysantha is paraphyletic or polyphyletic, containing three parallel lineages and Camellia longipedicellata (type of sectLongipedicellata) nested inside; 2) all four species from Vietnam, together with C. longipedicellata, forming a well supported monophyletic clade, which implies the close relationship between sect. Longipedicellata and sect.Chrysantha; and 3) sectLongissima is not monophyletic because C.hekouensis is the sister to the rest of Camellia species. The systematic position of C.longissima and the relationship between sect.Longissima and sect.Longipedicellata are unsolved.     

CHLOROPLAST DNA EVIDENCE FOR THE INTERRELATIONSHIPS OF TOMATOES,POTATOES, AND PEPINOS (SOLANACEAE)

We used chloroplast DNA restriction site analysis to test hypotheses of relationships of Solarium subgenus Potatoe (including potatoes and pepinos), two other Solanum, Cyphomandra (the tree tomatoes), and Lycopersicon (the tomatoes). Capsicum and Datura were used as outgroups. The results support two main clades among the taxa we studied: 1) Solanum subgenus Potatoe and Lycopersicon; and 2) other Solanum and Cyphomandra. Within the first clade, the following groups were supported: a) sect. Basarthrum and sect. Anarrhichomenum; b) sect. Etuberosum; c) sect. Petota; d) sect. Juglandifolium, including subsect. Lycopersicoides; and e) the genus Lycopersicon. These results, in combination with an analysis of morphological data, advocate the controversial, but previously suggested, treatment of Lycopersicon as congeneric with Solanum in subgenus Potatoe. Thus, the cultivated tomato will be recognized as Solanum lycopersicum L. Solanum chmielewskii and Solanum lycopersicum var. cerasiforme are proposed as new combinations; Solanum neorickii is proposed as a new name for Lycopersicon parviflorum. Our data also suggest that Cyphomandra should be included within Solanum.     

On Paphiopedilum malipoense sp. nov.—An Intermediate Form Between Paphiopedilum and Cypripedium,with a Discussion on the Origin of the genus

Paphiopedilum malipoense S. C. Chen et Tsi is a very interesting new species with its flower similar to that of Cypripedium, especially section Cypripedium. It belongs to subgenus Brachypetalum, the most primitive group of Paphiopedilum, but differs from its allied species in hgniva elliptic-lanceolate sepal with cuspidately acuminate apex, rather narrow petals and horizontal lip, which are of common occurrence in many cypripediums, but very rare in paphiopedilums. Apparently, this is an intermediate form, or a link, between Paphiopedilum and Cypripedium, but it does not seem to arise from hybridization between them, because no Cypripedium has been found wherever Paphiopedilum occurs. The new species is distributed in southeastern Yunnan of China. In this area, as well as in river valleys of western Yunnan or the Hengduan Mountains, there have been four species of the same genus reported before. As we know, the Hengduan Mountains and their adjacent areas are rich in Cypripedium. The differentiation of the genus there is remarkable. All five sections it contains occur there and three of them are quite distinctive. For example, the general appearance of the section Bracleosa is dissimilar to that of any other cypripediums, but closely resembles that of Listera. It appears that the difference between sect. Bracteosa of Cypripedium and sect. Brachypetalum of Paphiopedilum is not necessarily wider than that between sect. Bracteosa and sect. Cypripedium of the same genus. Apparently, it is reasonable to consider Paphiopedilum to be an evolutional branch of Cypripedium extending into tropical area, with its primitive group (subgenus Brachypetalum) still remaining in its northern fringe area. This primitive subgenus has eight species, distributed from western Yunnan to the Malay Peninsula. Five of them, including the intermediate and primitive form published here, are found in the hilly land of southeastern Yunnan and the river valleys of western Yunnan. All these facts suggest its area of origin: the river valleys of the Hengduan Mountains and the lower hilly land contiguous to the southof them.     

Taxonomy and Systematics of Some Species Groups of Saldula Van Duzee, with a Discussion of Riparian-Terrestrial Shifts in the Saldidae (Heteroptera)

Saldula lindbergi sp.n. is described from Cyprus, with additional material from Anatolia (Turkey), and is assigned to the Saltatoria-group with S. melanoscela (Fieber) as the closest relative. S. burmanica sp.n. is described from Kambaiti, N. E. Burma, and is close to S. orthochila (Fieber) (Orthochila-gmup). The Orthochila-group is discussed on the basis of S. orthochila, S. burmanica, S. nobilis (Horváth), and S. boucheriillei (Provancher) (non Sahla boucheriillei auct.). and details of male genital structures, pterygo-polymorphism, and habitat and zonal-geographic distribution are given. The inclusion of the Orthochila-group in the subgenus Macrosaldula , as proposed by Dethier in 1974. is rejected. The group is taking a somewhat divergent position in the genus and in some respects (e.g. secondary absence of the larval organ) it is approaching Salda Fabr. s.l. (Saldini). The radiative trends towards more terrestrial, dry-land habitats seen in the Orthochila-group are compared with similar trends in other taxa of the family. The serial affinities between most of the terrestrial habitats occupied by the Saldidae and riparian zones are emphasized. It is concluded that shifts towards more terrestrial habitats and habits are confined to some more advanced and derived–specialized lineages of the family, being an ecological feature mainly associated with a few boreal and mountainous taxa, which primarily inhabit drier, epilittoral stream-bank zones.     

Cyclopina (Copepoda, Cyclopoida) from Brazilian sandy beaches

Five new species of Cyclopina Claus are described and C. mediterranea Steuer is redescribed from Brazilian sandy beaches. Cyclopina curoli sp. n. can be very abundant in coarse sandy shows. It is related to C. laurentica Mocholls and C. crassisserosa Herbst with which it shares a similar structure of Leg 5 in the female. Cyclopina dorae sp. n. is most closely related to C. meditarranea Steuer. Cyclopina arenosa sp. n. and Cyclopina yutimaete sp. n. are reminiscent of C. pontica Monchenko, the only other species of Cyclopina that possess a 2-segmented endopod in leg 1. Cyclopina caissara sp. n. is distinguished from all other congeneric species by having a very reduced inner spine in the leg 5 exopod of both male and female. This species shares with C. schneideri Scott and C. schneideri and C. brevifurca Sars the 12–segmented antennule. Taxonomical problems related to C. schneideri and C. brevifurea are discussed. Cyclopina mediterranea Steuer, 1940 is recorded for the first time from the American continent.     

中国猎舞虻亚属二新种(双翅目,舞虻科)

记述我国猎舞虻亚属2新种.模式标本保存在中国农业大学昆虫博物馆.     

Phylogenetic relationships of Salvia (Lamiaceae) in China: Evidence from DNA sequence datasets

With 84 native species, China is a center of distribution of the genus Salvia (Lamiaceae). These species are mainly distributed in Yunnan and Sichuan provinces (southwestern China), notably the Hengduan Mountain region. Traditionally, the Chinese Salvia has been classified into four subgenera, Salvia, Sclarea, Jungia, and Allagospadonopsis. We tested this classification using molecular phylogenetic analysis of 43 species of Salvia from China, six from Japan, and four introduced species. The nuclear ribosomal internal transcribed spacer region and three chloroplast regions (rbcL, matK, and trnH-psbA) were analyzed by maximum parsimony, maximum likelihood, and Bayesian methods. Our results showed that the Chinese (except Salvia deserta) and Japanese Salvia species formed a well-supported clade; S. deserta from Xinjiang grouped with Salvia officinalis of Europe. In addition, all introduced Salvia species in China were relatively distantly related to the native Chinese Salvia. Our results differed from the subgeneric and section classifications in Flora Reipublicae Popularis Sinicae. We suggested that sections Eusphace and Pleiphace should be united in a new subgenus and that sect. Notiosphace should be removed from subg. Sclarea and form a new subgenus. Our data could not distinguish a boundary between subg. Allagospadonopsis and sect. Drymosphace (subg. Sclarea); the latter should be reduced into the former. Further clarification of the phylogenetic relationships within Salvia and between Salvia and related genera will require broader taxonomic sampling and more molecular markers.     

Systematics of Chimarrita, a new subgenus of Chimarra (Trichoptera: Philopotamidae)

The subgenus Chimarrita of the genus Chimarra is erected to include three described species, formerly placed in the subgenus Chimarra , and fifteen new species, all with distributions in the Greater Antilles or South America. A phylogeny for the species in the subgenus, and characters supporting monophyly of the subgenus Chimarrita , are proposed, as well as evidence for the monophyly of the subgenera Chimarra and Curgia . Keys are provided for the males and known females of the subgenus. Described species transferred to this subgenus are Chimarra simpliciforma Flint, Chimarra rosalesi Flint, and Chimarra maldonadoi Flint. Chimarra simpliciforma is designated the type species for the subgenus. New species in Chimarra ( Chimarrita ) described in this paper include: Chimarra akantha (Brazil), C . camella (Brazil), C . camura (Brazil), C . chela (Venezuela), C . forcipata (Venezuela), C . heligma (Brazil), C . heppneri (Peru), C . kontilos (Brazil), C . majuscula (Brazil), C . merengue (Dominican Republic), C . neblina (Venezuela), C . prolata (Ecuador), C . pusilla (Venezuela), C . tortuosa (Brazil), and C . xingu (Brazil).     

基于rDNA ITS序列探讨中国栽培灵芝菌株的亲缘关系

利用ITS序列分析技术对中国栽培灵芝菌株进行了亲缘关系分析。结果发现中国栽培灵芝菌株分布于5个聚类组,其中树舌亚属、紫芝组的菌株各自聚成一组,灵芝组的菌株分成3组,85·7%灵芝组菌株均聚于同一组,表明树舌亚属、紫芝组和灵芝组间的遗传差异较大,灵芝组内虽然存在着一定的遗传差异,但总体上亲缘关系比较近,遗传多样性并不丰富。聚类结果也表明仅仅根据形态学特征并不能将灵芝属菌株进行有效的分类,利用分子生物学的技术手段对灵芝菌种进行分类是一种更有效的方法。     

Three new species of Dactylicapnos (Fumariaceae) and a synopsis of the D. macrocapnos complex

The Dactylicapnos macrocapnos complex is revised, and D. platycarpa Lidén, D. odontocarpa Lidén and D. macrocapnos subsp. echinosperma Lidén are recognised as new taxa. The complex consists of a chain of 4 vicariant taxa from northwestern India (Garhwal) to western Bhutan (Thimphu). Dactylicapnos cordata Lidén (eastern Nepal, Darjeeling) is described and contrasted with its close relative, the geographically disjunct D. burmanica (western Yunnan, Burma).     

Notes on Corydalis sect. Corydalis in the Baltic area

The Nordic species of Corydalis sect. Corydalis are discussed. The name C. laxa has been applied to largeflowered forms of C. pumila , but also to C. solida and various hybrid derivates between them, and is superfluous as well as confusing. A lectotype for C. laxa is selected. The Baltic endemic Corydalis gotlandica is described. It is an allotetraploid derivative of C. solida and intermedia. Flora nordica notes no. 2.     

TAXONOMIC REVISION OF SARGASSUM SPECIES (FUCALES,PHAEOPHYCEAE) FROM NEW CALEDONIA BASED ON MORPHOLOGICAL AND MOLECULAR ANALYSES1

Sargassum C. Agardh (1820) is a taxonomically difficult genus distributed worldwide and reported as the most species‐rich genus of the Fucales. It is especially abundant in the Pacific where decreasing species richness is reported to occur from west to east. New Caledonia has been recognized as one of the hotspots of Sargassum diversity; however, species lists available for this region are old and incomplete and have not yet been updated with regard to the latest taxonomic revisions published. This study aimed at revising Sargassum diversity in New Caledonia and to assess its geographic affinities with neighboring Pacific regions. We used combined morphological and DNA analyses on new collections and examined numerous type specimens. Although 45 taxa have been listed in the literature, most of them have been either transferred to synonymy since or misidentified, and in this study, only 12 taxa were recognized as occurring in New Caledonia. They belong to the subgenus Sargassum sect. Binderianae (Grunow) Mattio et Payri (2), sect. Ilicifoliae (J. Agardh) Mattio et Payri (2), sect. Polycystae Mattio et Payri. (1), sect. Sargassum (4), sect. Zygocarpicae (J. Agardh) Setch. (2), and subgenus Phyllotrichia (Aresh.) J. Agardh (1). New Caledonian Sargassum flora appeared as the second richest in the region after the Pacific coast of Australia, with which it has shown high similarity, and shared species with all neighboring regions. One species, S. turbinarioides Grunow, is considered as endemic to New Caledonia. The low genetic diversity detected among several polymorphic species belonging to sect. Sargassum is also discussed.