Phylogenetic analysis of a polyphyletic African genus of Caesalpinioideae (Leguminosae): Monopetalanthus Harms

 To assess the new taxonomy of Monopetalanthus proposed by Wieringa, a phylogenetic study was performed using the chloroplast trnL intron and psbA-trnH spacer, and the nuclear ITS region of the 18-26S rDNA. The phylogeny clearly indicates the polyphyletic nature of Monopetalanthus. The molecular data support the transfer of M. longiracemosus to Tetraberlinia and the newly defined Aphanocalyx, which now includes all the previous Monopetalanthus species having leaflets with a marginal vein. Our analyses do not support the monophyly of the newly described genus Bikinia, which includes four new species and six species transferred from Monopetalanthus. Bikinia occurs either as paraphyletic with Tetraberlinia (chloroplast DNA data) or as a monophyletic group that also includes the new monotypic genus Icuria sister to Tetraberlinia (ITS data). Nonetheless, the molecular phylogeny generally supports the taxonomy of Wieringa in subdividing the genus Monopetalanthus into distinct groups, none of which retains the name Monopetalanthus. Received May 28, 2001; accepted July 6, 2002 Published online: November 20, 2002 Address of the authors: G. Y. Fannie Gervais, Anne Bruneau (e-mail: bruneaua@irbv.umontreal. ca), Institut de Recherche en Biologie Végétale, Université de Montréal, 4101 Sherbrooke est, Montréal, Québec, Canada, H1X2B2.     

Cytological study on the genus Syncalathium (Asteraceae‐Lactuceae), an endemic taxon to alpine scree of the Sino‐Himalayas

Abstract Cytological characters of four species in Syncalathium (Asteraceae: Lactuceae), a small genus with six identified species endemic to alpine scree of the Sino‐Himalayan region, are surveyed in this report. Three species (Syncalathium pilosum, Syncalathium chrysocephalum, and Syncalathium disciforme) are examined for the first time. Combined with our previous counts, five species have been cytologically investigated from the genus and the results indicated that all species are diploid with the basic somatic chromosome number of x=8. The karyotype asymmetry of Syncalathium souliei is 2A, distinct from the other four species of 1A, and the remaining species are divided into two subgroups with different karyotypes, consistent with their morphological features. The significance of the cytological evolution of Syncalathium is briefly discussed.     

中国特有属藤山柳属(猕猴桃科)植物的叶表皮形态及其分类学意义

由于形态特征变异和地理分布区域存在重叠,中国特有属藤山柳属(猕猴桃科)的物种划分问题长期以来存在争议,曾被分为20种或修订为含1种4个亚种的单型属。该研究选取了在形态和地理分布上有代表性的29个居群的184份标本,利用光学显微镜和扫描电镜观察了叶表皮形态和微形态特征,以探讨它们的分类学意义。结果表明:(1)藤山柳属植物叶表皮毛被的形态和微形态特征有3类,即光滑-短柱状毛、刚毛-长柱状毛/长刺毛、绒毛-单列多细胞毛,且这些特征在居群间差异明显,并各具明显的地理分布格局,支持把藤山柳属分为3类,即光滑类、刚毛类和绒毛类。(2)3类藤山柳植物在个别居群表现出部分同域分布现象,在峨眉山不同海拔高度的3个居群存在垂直地带性分布特点。(3)藤山柳属植物叶表皮的其他形态特征,如不规则型表皮细胞、6类气孔器、叶表皮初级蜡质纹饰以网状隆起为主,伴随着2～4类次级纹饰,在居群间变化多样等均没有明显的分类学意义。(4)由于具有相同的叶表皮形态特征和地理分布,建议把繁花藤山柳合并到绒毛藤山柳,故支持藤山柳属是1个正处于分化进程中的单型属,包括1个种3个亚种。     

A functional evenness index for microbial ecology

Microbial ecologists attempting to describe community structures through the use of synthetic parameters face enormous difficulties. These stem in part from the necessity of using standard taxonomic reference levels in a field where the species level is poorly defined. This paper presents an attempt to obviate this problem. A “functional evenness” index (E) is defined using information measures; it is based directly on the characteristics of the bacteria, as determined, for example, with the API 20B method. Comparisons of this index with classic structure indices, such as taxonomic evenness (Pielou) or systematic dominance (Hulburt), show that it behaves like an evenness index, while bypassing the taxonomic study required before computation of the classic indices. Its use is illustrated with samples of aerobic heterotrophic bacteria obtained from brackish lagoon sediments. We are grateful to our statistician colleagues, Dr. Yves Lepage from Université de Montréal and Dr. André Plante from Université du Québec à Montréal. Both have contributed important elements to the discussion presented in this Appendix.     

Invasion of American native lily populations by an alien beetle

The lily leaf beetle (Lilioceris lilii), indigenous to Eurasia, was first detected in North America on the island of Montréal, Québec, Canada in 1943. Populations remained limited to the original site of introduction but since 1978 the distribution of this species has expanded in all directions. To date L. lilii has only been recorded feeding on cultivated lilies in urban and rural areas. But as the beetle spreads its geographic range it could encounter native lily species. The objectives of this study were to determine the suitability of two indigenous North American lily species (Lilium canadense and L. philadelphicum) as host for L. lilii, and to assess the degree of infestation of wild lily populations. Measurement of fitness parameters under laboratory conditions (survival, development time, size) indicated that L. lilii has the capacity to develop on both species of native lilies. In the provinces of Québec and Ontario eight of the 20 wild populations of L. canadense sampled were infested. In contrast, L. philadelphicum was not attacked by the alien beetle. A number of native lilies are already endangered in North America, so there is an urgent necessity to address the ecological impact of L. lilii in natural ecosystems.     

A CYTOTAXOXOMIC SURVEY OF MELAMPODIUM (COMPOSITAE-HELIANTHEAE)

Turner , B. L.. and R. M. King . (U. Texas, Austin.) A cytotaxonomic survey of Melampodium (Compositae-Heliantheae). Amer. Jour. Bot. 49(3): 233–26. Illus. 1962.—Chromosome counts are reported for individuals from 89 populations of Melampodium representing 26 species The genus is multibasic with x = 9, 10, 11, 12, 16 and 23. Chromosome numbers on a base of x = 10 characterize the section Melampodium while basic numbers of x = 23, 16, 12, 11 and 9 occur in the section Zarabellia. Melampodium camphoratum (n = 16) differs from all other species examined in having relatively small meiotic chromosomes. Only 6 of the 23 species are polyploid or have polyploid races. Melampodium leucanthum and M. cinereum have both diploid and tetraploid populations; the latter occur without any apparent morphological or geographical correlation and are probably autoploid in origin. A survey of the basic chromosome numbers known for other genera of the subtribe Melampodinae (12 of 22 genera) is presented. and it is suggested that x = 10 is the most probable basic number of the genus and subtribe.     

Phenetic studies in Nuphar Sm. (Nymphaeaceae):variation in sect. Nuphar

Previous taxonomic assessments of the hydrophytic genus Nuphar Sm. (Nymphaeaceae) have inadequately considered the range of morphological variation existing in the genus. A comprehensive statistical analysis of morphological features among the recognized taxa of Nuphar is presented here, first using 10 fruit characters to delimit the separation of two infrageneric groups of taxa, and secondly using 31 characters to quantify the morphological variation found within sect. Nuphar. Results from combined phenetic analyses provided empirical support for recognition of two infrageneric groups of species in the genus (largely by fruit, stigmatic disk margin, neck, and stigmatic disk size) and for separation of taxa within sect. Nuphar (by leaf size, and fruit disk and neck size). Statistical analyses demonstrate that extensive variation in ranges of character states exists among sect. Nuphar taxa. However, a suite of qualitative and quantitative characters can be used to recognize five species and three subspecies within this predominantly Old World assemblage.     

Speciation and chromosomal evolution of the Palearctic species of chironomids of the genus Sergentia Kieffer (Diptera, Chironomidae): Divergence of the Karyotypes of S. baueri Wülker et al., 1999, S. prima Proviz et al., 1997, S. electa Proviz et al., 1999 and their relationship with the endemic species from Baikal lake

The banding structures of chromosomes of three Palearctic species of chironomids of the genus Sergentia Kieffer, 1922 from the Irkutsk reservoir were comparatively analyzed: S. baueri Wülker et al., 1999 (2n = 8), S. prima Proviz et al., 1997 (2n = 8), and S. electa Proviz et al., 1999 (2n = 6). The S. baueri karyotype was taken as a standard in chromosome mapping. It was established that in contrast to S. baueri and S. prima the S. electa karyotype was formed due to a complex translocation: transfer of chromosome IV in the median part of chromosome III. The sequences of chromosome I bands were found to be completely homologous in all Palearctic species and in S. rara Proviz et al., 1999 (2n = 8) taken as the original species in the group of Baikalian endemics. In both groups, seven homozygous inversions were detected, of which the common one is the inversion in chromosome III. It was assumed on the basis of the results of the karyological analysis that among the Palearctic species S. baueri is most similar to the Baikalian endemics and S. electa is phylogenetically closer to S. prima. Specific features of the chromosome and morphological evolutions of the Sergentia genus species are considered.     

NOTES ON SOME GRASSES. XVI. EMBRYO STRUCTURE OF THE GENUS ORYZA IN RELATION TO THE SYSTEMATICS

Three distinct types of embryo have been found in 18 species of the genus Oryza. Type 1 is characterized by lateral fusion of the epiblast and the scutellum and also by the development of auricles. Type 2 has no auricle, and the epiblast is not laterally fused with the scutellum. Type 3 has a cleft between the lower part of the scutellum and the coleorhiza, a long epiblast which is free from the scutellum, and lacks auricles. Type 1 has been found in 13 species of section Sativae, Type 2 in 4 species of sections Granulatae and Coarctatae, and Type 3 in O. coarctata only. The results indicate that species of section Sativae are more or less closely related, while section Coarctatae is a heterogeneous group. A new section, Ridleyianae, has been described for Oryza ridleyi and some other species. Oryza coarctata has unique features in embryo structure, morphology and leaf anatomy, and this species has been moved from the genus Oryza to a separate genus, Sclerophyllum, which is here revived.     

Patterns of trait variation in the diploid wheats (Triticum,Aegilops) and the tetraploid speciesTriticum diccocoides

Eighteen earliness and morphological traits were examined in from 2 to 14 lines each of 10 diploid members of the wheat complex,Triticum-Aegilops, and 15 lines of the tetraploid speciesTriticum diccocoides. In general, earliness traits have the greatest relative between line vs. within line variation of all the traits examined. Within species, earliness traits are the principle set of characters around which evolve between line trait differences, one of the most important oich is leaf dimensions. At the genus level, earliness traits are independent of leaf dimensions and plant height characters. Thus, the pattern of evolution at the genus level is different from that exhibited in each of the species. Biological and evolutionary implications of these findings are discussed.     

CHROMOSOME NUMBERS AND PHYLOGENY IN MELAMPODIUM (COMPOSITAE)

The haplord chromosome numbers of n = 9, 10, 11, 12, 18, 20, 23, 25 ± 1, 27, 30, and 33 have been reported by various authors from 26 of the 37 recognized species of Melampodium. A chromosomal survey of 375 plants from 275 different populations suggests that the recorded numbers are stable within the genus and that infraspecific euploidy and aneuploidy are uncommon. These chromosome numbers can be arranged numerically, with morphological and limited cytogenetic substantiation, into four euploid series of x2 = 9, 10, 11, and 12. Of these four groups of species, the x = 10 series is the largest and morphologically most diverse. This consideration, along with additional evidence from the morphology of sterile disc ovaries, suggests that x = 10 is the ancestral chromosomal base in Melampodium. A comparison of morphological and cytological data from the closely related genera, Acanthospermum and Lecocarpus, indicates that the latter are probably on a common base of x = 11. Present day distributional patterns of all three genera support the hypothesis that x = 10 is the ancestral base for the entire complex.     

凤仙花近缘种间核型分析与叶表皮微形态研究

为探究凤仙花近缘种植物的细胞学和微形态学方面的亲缘关系,该文选取荔波凤仙花(Impatiens liboensis)及近缘种赤水凤仙花(I.chishuiensis)和管茎凤仙花(I.tubulosa)的根尖和叶表皮为实验材料,采用体细胞染色体常规压片法和叶表皮光学显微镜观察法对凤仙花近缘种植物进行染色体及叶表皮特征研...     

国产柿属(Diospyros)的叶表皮形态研究及其分类学意义

为了解柿属(Diospyros)植物的叶表皮特征,在光学显微镜下观察了46种2变种植物的叶表皮微形态特征,并进行了主成分分析。结果表明,柿属植物的叶表皮微形态可分为2组：A组的表皮细胞为不规则形,垂周壁浅波状或深波状;B组的表皮细胞为多边形,垂周壁平直或弓形。气孔全部位于下表皮,以无规则型为主,但同时有辐射型、环列型和十字型气孔存在。大多数种具有表皮毛,表皮毛有非腺毛和头状腺毛的区别。柿属植物的叶表皮微形态特征类型多样,能够为部分类群的分类提供较好的形态学证据。     

CYTOGENETIC STUDIES OF SOME HYPOCHOERIS SPECIES (COMPOSITAE) FROM BRAZIL

Karyotypes of nine Brazilian taxa of genus Hypochoeris were studied utilizing root-tip mitotic metaphases. Two distinct groups were found. One group includes six species that showed high asymmetric bimodal karyotypes, while the second group has two species that have a karyotype similar to those observed in European species. All the species have karyotypes with 2n = 8 that are very uniform within each group, with only small morphological differences. Nucleolar organizing region and C-band patterns are shown for H. brasiliensis.     

Four new species of Typhlocharis (baetica group) (Coleoptera: Carabidae: Anillini) from southwestern Iberian Peninsula with notes on their biogeographical and morphological implications

Four new species of Typhlocharis (Carabidae: Anillini) are described from the southwest of the Iberian Peninsula, assigned to the baetica species group. T. prima sp.n. , T. secunda sp.n. and T. tertia sp.n. (from La Palma del Condado, Huelva, Spain) are syntopic, and T. quarta sp.n. (from Barrancos, Beja, Portugal) is the first species of the group with umbilicate series 4 + 4. They represent, respectively, the southernmost and westernmost distribution data for the group. The baetica group remains well defined and includes ten species. The diagnosis is simplified, with the confirmation that many morphological features characteristic of this group are widespread within the genus. The defining character is the presence of denticles in apical margin of elytra, not associated to the seventh stria or to the elytral suture. The new species provide morphological data that suggest the baetica and silvanoides groups are closely related. Distribution of both groups in the south of the Iberian Peninsula and the presence of morphological characters that are considered plesiomorphic are coherent with the hypothesis of betic‐riffain origin of the genus. They also support the hypothesis of easy alteration of the umbilicate pattern between closely related species and the independent origin of apical denticles in the group compared with those present in other species of the genus. The presence of three well‐differentiated size ranges in syntopic populations suggest ecological diversification to avoid interspecific competition.     

贵州30种杜鹃属植物叶背表皮显微形态特征

杜鹃属植物的分类历来都十分重视叶片表皮特征的分类学价值,无论是在各亚属之间还是在种及种下等级的划分中都很强调此类特征的作用。贵州省位于世界现代杜鹃分布中心边缘及向东部散布的过渡地带,省内自然分布的杜鹃种类资源丰富而又独具特色,包括很多尚未深入研究的特有类群。为进一步研究贵州杜鹃属植物的属下系统分类关系,该文对自然分布于贵州的30种杜鹃进行了叶背显微形态特征研究,其中有28种的叶背表皮特征为首次报道。研究材料全部来自采于贵州西北部百里杜鹃自然保护区内的杜鹃属植物,包括杜鹃亚属4种、糙叶杜鹃亚属1种、常绿杜鹃亚属22种、马银花亚属1种及映山红亚属2种,共计30种。研究方法为取成熟叶片处理后在JSM-6490型扫描电镜下对叶背表皮进行观测。叶背鳞片类型的划分方法参照前人工作。结果表明:这30种杜鹃叶片叶背表皮形态特征在电子显微镜下表现出明显的多样性,如有鳞类杜鹃具有鳞片而其他类群则无,叶表面有或无表皮毛,表皮毛排列稀疏或密生,气孔器未见或偶见,散生于乳突状或非乳突状突起之间,或角质层增厚气孔器下陷,内、外拱盖表面粗糙或光滑,气孔器周围有或无间断的条形突起,突起呈环状或羽状等,但在同一亚属或亚组中又呈现出或多或少的一致性。研究讨论表明,叶背表皮显微形态特征在杜鹃属植物的属下系统分类中具有重要的研究价值。     

Revision of the systematics of the genus Calliptamus Serville 1831, (Orthoptera: Acrididae: Calliptaminae) in Algeria using morphological,chemical, and genetic data

Summary. The genus Calliptamus contains swarming orthopterans that cause serious damage in Algerian agricultural systems. However, it remains difficult to identify species within this genus; a thorough understanding of the group’s systematics and the utilization of novel taxonomic criteria are needed. We used morphological analysis along with two other methods of species identification – chemotaxonomy with cuticular compounds and DNA barcoding involving the COI gene – to classify 81 individual grasshoppers collected at two different sites in the Sétif region (northeastern Algeria). The chemotaxonomic analyses yielded ambiguous results, but DNA barcoding allowed us to differentiate two Calliptamus species found in Algeria: Calliptamus barbarus (Costa 1836), and Calliptamus wattenwylianus (Pantel 1896). Several morphological criteria used in identification keys appear to reflect differences among morphotypes rather than differences between species, and their taxonomic specificity is not supported by the barcoding data. The number of spines on the hind tibia is the only morphological criterion that reflected genetic differences between species; it is thus considered to be a taxonomically useful feature for identifying species in this genus.     

New chromosome counts and evidence of polyploidy in Haageocereus and related genera in tribe Trichocereeae and other tribes of Cactaceae

Chromosome numbers for a total of 54 individuals representing 13 genera and 40 species of Cactaceae, mostly in tribe Trichocereeae, are reported. Five additional taxa examined belong to subfamily Opuntioideae and other tribes of Cactoideae (Browningieae, Pachycereeae, Notocacteae, and Cereeae). Among Trichocereeae, counts for 35 taxa in eight genera are reported, with half of these (17 species) for the genus Haageocereus. These are the first chromosome numbers reported for 36 of the 40 taxa examined, as well as the first counts for the genus Haageocereus. Both diploid and polyploid counts were obtained. Twenty nine species were diploid with 2n=2x=22. Polyploid counts were obtained from the genera Espostoa, Cleistocactus, Haageocereus, and Weberbauerocereus; we detected one triploid (2n=3x=33), nine tetraploids (2n=4x=44), one hexaploid (2n=6x=66), and three octoploids (2n=8x=88). In two cases, different counts were recorded for different individuals of the same species (Espostoa lanata, with 2n=22, 44, and 66; and Weberbauerocereus rauhii, with 2n=44 and 88). These are the first reported polyploid counts for Haageocereus, Cleistocactus, and Espostoa. Our counts support the hypothesis that polyploidy and hybridization have played prominent roles in the evolution of Haageocereus, Weberbauerocereus, and other Trichocereeae.     

Phylogeny, morphology, and biogeography ofChuquiraga, an Andean-Patagonian genus of Asteraceae-Barnadesioideae

Chuquiraga is a genus of 23 species of evergreen shrubs endemic to South America. It is distributed principally along the Andes from Colombia to Chile and Argentina, and it is especially diversified in the Central Andes and in the deserts and semideserts of southern South America. The genus exhibits a wide array of leaf-morphology types and two different head and floral types apparently related to hummingbird and insect pollination. In this study, phylogenetic relationships amongChuquiraga species were resolved by parsimony cladistic analysis using morphological characters. The resulting cladogram was used to interpret morphological, ecological, and biogeographical patterns in a historical context. Biotic and abiotic environmental factors hypothesized to have exerted selective pressure on morphological traits of its species were optimized onto the phylogeny to suggest how and when these factors may have affected the evolution and diversification of the genus. Results suggest an origin of the genus in southern South America, with two major evolutionary radiations, one more northern in the Central and Northern Andes, and the other in the Southern Andes and the North Chilean, Patagonia and Monte Deserts. Pollination by hummingbirds seems to have been an important factor in the origin of the northern clade, affecting floral morphology. Herbivory by vertebrates and increased aridity seem to have been important selective forces in the evolution and diversification of the southern clade, especially affecting leaf morphology. These changes were probably associated with the major elevation of the Andes in late Tertiary and with the hyperaridization and climatic fluctuations of Pleistocene and Holocene times.

---

Resumen   Chuquiraga es un género con 23 especies de arbustos perennifolios endémico de América del Sur. Se distribuye principalmente a lo largo de los Andes desde Colombia hasta Chile y Argentina y está especialmente diversificado en los desiertos y semidesiertos de América del Sur. El género presenta un amplio espectro de tipos de morfología foliar y dos tipos florales y de capítulos aparentemente relacionados con la polinización por colibríes y por insectos. En este trabajo las relaciones filogenéticas entre las especies deChuquiraga se resolvieron mediante análisis cladístico de parsimonia utilizando caracteres morfológicos. El cladograma resultante se empleó para interpretar patrones morfológicos, ecológicos y biogeográficos de las especies en un contexto histórico. Factures bióticos y abióticos que se han hipotetizado que han ejercido presión selectiva sobre los caracteres morfológicos fueron optimizados sobre la filogenia para sugerir cómo y cuándo podrían haber afectado la evolución y la diversificación del género. Los resultados obtenidos sugieren un origen del género en el sur de América del Sur, y dos principales radiaciones evolutivas, una más al norte en los Andes Centrales y en los Andes del Norte, y la otra más al sur en los Andes del Sur y en los desiertos del norte de Chile, la Patagonia y el Monte. La polinización por colibríes parece haber sido un factor importante en el origen del clado del norte, afectando la morfología floral. La herbivoría por vertebrados y el incremento en la aridez parecen haber sido fuerzas selectivas importantes en la evolución y diversificación del clado austral, afectando especialmente la morfología foliar. Estos cambios probablemente estuvieron asociados a la elevación máxima de los Andes a fines del Terciario y a la hiperaridización y fiuctuaciones climáticas del Pleistoceno y Holoceno.