The flagellar apparatus ofMesostigma viride (Prasinophyceae): Multilayered structures in a scaly green flagellate

Mesostigma viride Lauterborn (Prasinophyceae) is the first green flagellate found to have multilayered structures (MLS) in its flagellar apparatus. MLS's were previously known from green algae only in charophycean swarmers, linking theCharophyceae to the origin of land plants, whose male gametes (when flagellated) also possess an MLS.M. viride is, therefore, probably more closely related to the origin of theCharophyceae than any other green flagellate that has been thoroughly studied so far. The occurrence of MLS's in green flagellates and apparently in other algae and protozoans suggests that an MLS occurred in an ancient group of flagellates and has survived in various protistan lines, including the line of green algae related to land plants. The occurrence of a synistosome inM. viride and other of its characteristics suggest that it is more closely related toPyramimonas than to other genera of scaly green flagellates.This work was supported by National Science Foundation Grant DEB-78-03554.     

Flagellar apparatus ultrastructure inMesostigma viride (Prasinophyceae)

The ultrastructure of the flagellar apparatus ofMesostigma viride Lauterborn (Prasinophyceae) has been studied in detail with particular reference to absolute configurations, numbering of basal bodies, basal body triplets and flagellar roots. The two basal bodies are interconnected by three connecting fibers (one distal fiber = synistosome, and two proximal fibers). The flagellar apparatus shows 180° rotational symmetry; four microtubular flagellar roots and two system II fibers are present. The microtubular roots represent a 4-6-4-6-system. The left roots (1s, 2s) consist of 4 microtubules, each with the usual 3 over 1 root tubule pattern. Each right root (1d, 2d) is proximally associated with a small, but typical multi-layered structure (MLS). The latter displays several layers corresponding to the S₁ (the spline microtubules: 5–7), and presumably the S₂—S₄ (the lamellate layers) of the MLS of theCharophyceae. At its proximal origin (near the basal bodies) each right root originates with only two microtubules, the other spline microtubules being added more distally. The structural and positional information obtained in this study strongly suggest that one of the right roots (1d) ofMesostigma is homologous to the MLS-root of theCharophyceae and sperm cells of archegoniate land plants. Thus the typical cruciate flagellar root system of the green algae and the unilateral flagellar root system of theCharophyceae and archegoniates share a common ancestry. Some functional and phylogenetic aspects of MLS-roots are discussed.Dedicated to Prof. DrLothar Geitler on the occasion of his 90th birthday.     

Phylogenetic analysis ofUlmaceae

A phylogenetic analysis of theUlmaceae, Cannabaceae, Barbeyaceae, andBroussonetia of theMoraceae produced nine equally parsimonious trees with 127 steps. TheUlmoideae (Ulmaceae, sensuGrudzinskaya) are a monophyletic group and distinct from theCeltidoideae. The genusAmpelocera occupies an isolated taxonomic position among the celtidoids. The similarity ofAmpelocera to the fossil celtidoid flowerEoceltis of North America suggests thatAmpelocera posesses an archaic suite of characters, and occupies a primitive position among the celtidoids, theCannabaceae and theMoraceae. The relationships among the other celtidoid taxa,Cannabaceae, andBroussonetia are problematic. TheCannabaceae andBroussonetia of theMoraceae are nested within the celtidoids suggesting that this is a paraphyletic group. The close, but unresolved, relationship of the celtidoids to theMoraceae andCannabaceae observed in this analysis, and the appearance of the celtidoids in the fossil record prior to the ulmoids suggests that the evolutionary relationship of the ulmoids and celtidoids may be more distant than current taxonomic treatments reflect.     

Taxonomy and phylogeny of the tribePlucheeae (Asteraceae)

The tribePlucheeae (Benth.)A. Anderb., has been analysed cladistically by means of a computerized parsimony program (Hennig 86), using theArctotideae as outgroup. The results of the analysis are presented in a consensus tree and one cladogram. Four major monophyletic subgroups can be recognized: TheColeocoma group (3 genera), thePterocaulon group (3 genera), theLaggera group (6 genera), and thePluchea group (12 genera). All recognized genera are described and most genera are supplied with taxonomical notes including comments on their taxonomic status. Genera such asBlumea, Pluchea, andEpaltes are demonstrated to be unnatural assemblages.Monarrhenus andTessaria are both closely related to thePluchea complex. The old generic nameLitogyne Harv. has been taken up for one species ofEpaltes, the genusRhodogeron is reduced to a synonym ofSachsia, and the following new combinations are made;Litogyne gariepina (DC.)A. Anderb., andSachsia coronopifolia (Griseb.)A. Anderb.     

Heliantheae sensu lato (Asteraceae), clades and classification

The interrelationships within theHeliantheae s. lato and the closely relatedEupatorieae are analyzed and discussed. The basis to this discussion is a cladistic analysis of 141 morphological characters (172 apomorphic states) scored for 97 genera. TheHeleniae s. lato, a subgroup of theHeliantheae s. lato, are paraphyletic, and a monophyletic group corresponding largely to theHeliantheae s. str. is recognized. TheEcliptinae sensuRobinson are polyphyletic. TheCoreopsidinae form an ingroup in theHeliantheae s. str. TheTageteae (Pectidinae) and theMadieae (Madiinae) are two separate branches within the helenioid assemblage of taxa.     

Comparative cytology and taxonomy of theUlvaphyceae II. Ulvalean characteristics of the stephanokont flagellar apparatus ofDerbesia tenuissima

Summary The stephanokont flagellar apparatus of the zoospores ofDerbesia tenuissima (De Not.) Crouan is examined and compared to the flagellar apparatuses of other green algae. The flagella ofDerbesia are attached to two of three bands which lie at the junction of the body and papilla. Serial longitudinal and cross sections reveal that the basal bodies are attached to the bands along their sides and at their proximal ends. The bands are not striated in any plane. The lack of striation in the bands and the partial covering of the proximal end of the basal bodies by one of the bands closely resemble the type of flagellar connection system described as the Bryopsis-type byMelkonian (1980). Zoospores of ulvalean green algae also possess these features, suggesting that green siphons are phylogenetically related to theUlvales. It is proposed that green siphons be tentatively classified in theUlvaphyceae rather than in theChlorophyceae orCharophyceae.This work supported by NSF Grant DEB 78-03554.     

Interspecific hybridizations among species of theElymus semicostatus andElymus tibeticus groups (Poaceae)

Interspecific hybridizations were made between species of theE. semicostatus group, viz.,E. semicostatus (Nees exSteud.)Meld.,E. validus (Meld.)B. Salomon,E. abolinii (Drob.)Tzvel., andE. fedtschenkoi Tzvel., and species of theE. tibeticus group, viz.,E. pendulinus (Nevski)Tzvel.,E. tibeticus (Meld.)Singh,E. shandongensis B. Salomon, andE. gmelinii (Ledeb.)Tzvel., as well as among species within theE. tibeticus group. All species are tetraploid (2n = 4x = 28) and possess SY genomes. Meiotic pairing data from 24 hybrids involving 17 interspecific combinations are presented. The average number of chiasmata per cell ranged from 17.91 to 26.20 in hybrids within theE. tibeticus group, compared with 7.26 to 22.04 in hybrids between the two species groups. Despite the extensive collection of cytological data, there was no definite evidence for confirming or disproving the separate existence of the two groups.     

Systematic relationships of theSaxifragales revealed by serological characteristics of seed proteins

Comparative investigations of serological characters of seed proteins from taxa regarded as members of theSaxifragales result in the recognition of two distinct groups of related families. One consists of theSaxifragaceae, Grossulariaceae, andCrassulaceae; to itHamamelis, and possiblyPenthorum and theRosaceae may be connected. The second group contains theHydrangeaceae, Escalloniaceae, Roridulaceae, Cornaceae, andCaprifoliaceae; it is rich in iridoid compounds, has more derived morphological characters, and seems to represent a monophyletic line block. ThePittosporaceae were not found to be linked with either of the two groups, but rather show similarities with members of theApiales. All these data support systematic arrangements proposed byDahlgren (1975a).     

Biostatistical studies on western EuropeanDactylorhiza (Orchidaceae)—theD. maculata group

Multivariate analysis tools are exploited on a data set composed of quantitative characteristics collected on 35 populations of plants of theDactylorhiza maculata (L.)Soó group from Western-Europe. These samples lead to four well-defined clusters; this, together with qualitative, cytological and ecological arguments, allows for the recognition of four specific entities:D. maculata s.str.,D. fuchsii (Druce)Soó,D. saccifera (Brongn.)Soó andD. caramulensis (Vermeulen)Tyteca. It is concluded that the floral characters play an essential role in the taxonomical distinction. It also appears that the set of characters measured, as well as the methods exploited, are especially well-suited and valuable tools for the morphological study of the genusDactylorhiza.     

The application and citation of the generic nameParmeliopsis (Lecanorales,Parmeliaceae)

The nomenclatural history of the generic nameParmeliopsis is reviewed. Its correct citation is found to beParmeliopsis (Nyl. exStizenb.)Nyl., dating from 1866, not 1869 as commonly cited, withP. placorodia (Ach.)Nyl. as holotype species. There is consequently no nomenclatural problem to the adoption ofForaminella Fricke Meyer, typified byF. ambigua (Wulfen)Fricke Meyer for theParmeliopsis species with falcate conidia. A synopsis of the nomenclature of the North American and European species of both these genera is included.     

Die Stipeln derIrvingioideae undRecchioideae und ihre systematische Wertung nebst Bemerkungen zur Holzanatomie und Palynologie

TheSimaroubaceae generally have no true stipules. The stipule-like appendages of some genera proved to be pseudo- or metastipules (Weberling & Leenhouts 1965). There seem to be some exceptions, however: the generaCadellia (incl.Guilfoylia) andRecchia on the one hand, and theIrvingioideae on the other. As these taxa, with exception ofRecchia, have simple leaves, there are no indications that their stipule-like appendages might be pseudo- or metastipules. In regard to their position and ontogeny these appendages behave completely like true stipules. Assuming the view ofForman, one could conceive a morphological line from the long, broadly inserted axillary stipules of mostIrvingioideae to the small scaly triangular stipules ofIxonanthoideae. The similarities between the stipules ofIrvingioideae andErythroxylaceae (already emphasized byHallier and others), become even more evident when their ontogeny is investigated. TheIrvingioideae, therefore, might be regarded as a separate family (perhaps with some relation to theErythroxylaceae,Hallier) or as a subfamily ofIxonanthaceae (Forman).—In addition to data on stipules some results on the palynology and shoot anatomy of the generaCadellia (incl.Guilfoylia) andRecchia are reported. Their relationship with theSimaroubaceae also appears doubtful. If they are to be included, they represent a somewhat isolated group near the base of the family which otherwise has lost its stipules.

Herrn Univ.-Prof. Dr.Walter Leinfellner zum 70. Geburtstag gewidmet.     

The genusIschnea (Asteraceae,Senecioneae) in New Guinea

The endemic New Guinean genusIschnea F. Muell. (Asteraceae, Senecioneae, Blennospermatinae) is revised and four species are recognized. Characters of special interest are tubeless ray florets, male disc florets, and secretory spaces in leaves. A principal component analysis is made on theIschnea elachoglossa F. Muell. complex which shows great variation. One new species,I. capellana Swenson, from the Star Mountains, is described. A key, illustrations, and distribution maps to all species are supplied.     

Probleme der Infloreszenztypologie vonW. Troll

In contrast toW. Troll's typology of inflorescences which aims at more or less rigid, well defined types, this investigation accentuates the processes that constitute the evolutionary transformations leading from one typical form to another.Troll divided the inflorescences into the two types of monotelic and polytelic synflorescences, the first with a terminal flower on the main axis, the latter with a homogeneous florescence on the indeterminate axis. Both forms are enriched by proximal branches which repeat the structure of the main axis (paracladia). The evolutionary processes leading from the more primitive monotelic type to the advanced polytelic type are truncation (loss of the terminal flower) and homogenization of the distal branches, which thus form a homogeneous florescence. A closer survey of the polytelic groups reveals the fact that, usingTroll's criteria, the same distinction can be found within these groups themselves. Loss of the terminal florescence (truncation of 2nd and higher degree) as well as homogenization of the distal paracladia may lead to florescence-like units of higher complexity. Examples can be found inAsteraceae (Figs. 1 and 2),Fabaceae (Fig. 3 a),Mimosaceae (Fig. 3 b),Acanthaceae, and also in Monocots, as exemplified by theMarantaceae (Figs. 4 and 5). The so-called racemization (inversion of efflorescences from basipetalous to acropetalous) may be mentioned as a third element of transformation, emphasizing the unity of the florescences.—In consequence, there are more organizational levels than reflected in the twoTroll types. The polytelic type comprises several degrees of truncation and homogenization, the basis for a reasonable organizational analysis should therefore be the degree of ramification of flowering branches rather than the mere question of a terminal flower on the main shoot axis (Fig. 6). On the other hand the three processes of truncation, homogenization and racemization are evolutionary transformations that may occur independently from one another, thus giving rise to a large number of variations, which can not be satisfactorily interpreted by exactly defined types. On the basis of these considerations the question of homologous parts in inflorescences is reviewed. The homology of partial florescences and paracladia is accentuated contrary toTroll's interpretation (Fig. 7). Homogenization as an evolutionary trend may transform paracladia of different degree of ramification, leading to one-flowered units on the one side and to highly complex structures as in theMarantaceae on the other.

     

Neoschumannia (includingSwynnertonia), a primitive genus of theAsclepiadaceae-Stapelieae

A comparison of the West AfricanNeoschumannia Schltr. and the East AfricanSwynnertonia S. Moore reveals that the two monotypic genera must be united.Swynnertonia is sunk into synonymy ofNeoschumannia and the new combinationNeoschumannia cardinea (S. Moore)Meve is made for the East African species.Neoschumannia is shown to belong to the tribeStapelieae. The taxon exhibits a very unusual character combination: the growth form of a woody liana is combined with a tripartite corona unique within theAsclepiadaceae. The morphology of the corona suggests a position ofNeoschumannia close to the base of theStapelieae —Ceropegiinae alliance.     

Phylogenetic relationships of epacrids and vaccinioids (Ericaceae s. l.) based onmatK sequence data

Cladistic relationships of epacrids and vaccinioids (Ericaceae) are investigated using nucleotide sequence data from the chloroplast encodedmatK gene. Sequences of 56 taxa were aligned and analyzed using parsimony methods. Results show thatVaccinioideae as currently recognized are not monophyletic. The epacrids are sister to a clade that includes theLyonia group, theGaultheria group, and theVaccinieae. Arbutus andPyrola branch early inEricaceae, before the rhododendroid group.Enkianthus is sister to the remainingEricaceae (includingEpacridaceae).Vaccinieae are strongly supported as monophyletic, butVaccinium andAgapetes are polyphyletic.     

Phylogenetic relationships ofSphaerophoraceae (Ascomycetes) inferred from SSU rDNA sequences

SSU rDNA was sequenced from the lichenized fungiBunodophoron scrobiculatum andLeifidium tenerum (Sphaerophoraceae), andStereocaulon ramulosum andPilophorus acicularis (Stereocaulaceae) and analysed by maximum parsimony with 44 homologous ascomycete sequences in a cladistic study. A small insertion (c. 60 nt.) was found in the sequence ofLeifidium tenerum. Sphaerophoraceae constitutes a strongly supported monophyletic group which groups together withLecanora dispersa and theStereocaulaceae. Together withPorpidia crustulata, this larger group is a sistergroup to thePeltigerineae. This analysis thus supports theLecanorales as monophyletic, includingSphaerophoraceae and thePeltigerineae, but does not provide strong support for this monophyly. The analysis also suggests that the prototunicate ascus in theSphaerophoraceae is a reversion to the plesiomorphic state. Based on morphological, anatomical and chemical reasons,Sphaerophoraceae is proposed to belong to one of the groups presently included in the paraphyletic suborderCladoniineae within theLecanorales.     

Studies on the early floral development inCleomoideae (Capparaceae) with emphasis on the androecial development

Floral ontogeny ofCleome spinosa, Cleome violacea andPolanisia dodecandra subsp.trachysperma was studied in the context of the question whether the fascicled androecium ofReseda andCapparis (with fused fascicles) or the 2 + 4-pattern of theBrassicaceae is primitive in theCapparales. InPolanisia dodecandra, the 9–18 stamens show unidirectional initiation from the adaxial side toward the abaxial side of the flower. InCleome violacea, the six stamens also are formed in an unidirectional order, but development starts abaxially and a zigzag-like pattern is superimposed. InCleome spinosa, two stamen primordia in transversal (lateral) position are followed by four stamens which arise on a somewhat higher level in two pairs in front of the median sepals. It is assumed that the evolutionary steps in the androecial development proceed fromReseda viaCapparis andPolanisia/Cleome toBrassicaceae. This interpretation is supported byrbcL-studies (Chase & al. 1993,Rodman & al. 1993).Dedicated to emer. Univ.-Prof. DrFriedrich Ehrendorfer on the occasion of his 70th birthday     

Heteromerikarpie und Fruchtpolymorphismus beiMicroparacaryum,gen. nov., (Boraginaceae)

Microparacaryum (M. Pop. exH. Riedl)Hilger & Podlech is described as a new genus of theBoraginaceae-Cynoglosseae. It comprises the annual species hitherto included inParacaryum (DC.)Boiss. andMattiastrum (Boiss.)Brand. Distribution maps are given for all 3 genera.Microparacaryum consists of two species,M. salsum (Boiss.)Hilger & Podlech (M. s.) andM. intermedium (Fresen.)Hilger & Podlech (M. i.). ParticularlyM. i. is a very variable species, and most of the species formerly recognized belong here. Scattered all over the range of the genus, plants occur with nutlets exhibiting flat or incurved marginal wings, often in mixed populations. This fruit polymorphism is taxonomically treated by recognizing formae. In addition, the following new infraspecific taxa and combinations are described:M. i. var.intermedium formaparacaryoides Hilger & Podlech,M. i. var.stellatum (H. Riedl)Hilger & Podlech,M. i. var.stellatum formamattiastroides Hilger & Podlech,M. s. formamattiastroides Hilger & Podlech.

     

A numerical taxonomic study of thePolygonum aviculare complex (Polygonaceae) in Belgium

16 morphological characters were assessed in 300 plants sampled from 27 populations ofPolygonum aviculare sensu lato representative of the whole ecological range of the species in Belgium. The three multivariate treatments performed, namely principal component analysis, cluster analysis and discriminant analysis provide evidence thatP. aviculare can be divided in 4 units, roughly corresponding to the four taxa recognized byChrtek. However, the results point out that subsp.monspeliense and subsp.calcatum should be included at the varietal rank within respectively subsp.aviculare (=P. heterophyllum) and subsp.aequale (=P. arenastrum) as defined byLindman. Fruit dimensions, fruit shape and tepal length are the most discriminant characters for separating the four taxa, while several other characters are discriminant at the population level only. The evolutionary significance of the variation pattern of the whole complex is discussed in terms of life history differentiation and ecological specialization.     

Systematik,Verbreitung und Karyologie derFestuca violacea-Gruppe (Poaceae) im Ostalpenraum

The biosystematics of theFestuca violacea group (F. rubra subsp.violacea sensuHackel) in the Eastern Alps is studied.F. picturata Pils (=F. picta Kit. exSchultes nonJ. F. Gmelin) is confirmed as diploid, whereas the chromosome numbers forF. nitida (diploid),F. puccinellii (hexaploid), andF. norica (diploid, tetraploid and hexaploid) are reported for the first time. Details of morphology, leaf anatomy, and epidermal structures now allow a better separation of these species; new maps illustrate their distribution. Karyological, chorological, morphological, and anatomical data form the basis for a discussion of the phylogeny of theF. violacea group and its position withinF. rubra s. latiss.