Studies in Heterobasidiomycetes,Part 38*)Sphacelotheca polygoni-persicariae G. Demi & Oberw. spec. nov.

A new species, Sphacelotheca polygoni-persicariae, parasitizing the ovaries of Polygonum persicaria L. is described. This smut, collected several times in Madeira, Portugal, differs from other species of that genus, by its host plant and the reticulated teliospore ornamentation. On the basis of the morphological and ultrastructural characters of S. polygoni-persicariae, in connection with some recently published data on siderophore formation and 5S ribosomal RNA sequences it can be assumed that 1) members of the genus Sphacelotheca are separated from typical Ustilago species of Poaceae, 2) Sphacelotheca is restricted to species parasitizing Polygonaceae, and 3) species of Sphacelotheca and Microhotryum as well as those Ustilago species which parasitize in the flowers of Polygonaceae are closely related.     

AMPHIDINIUM REVISITED. II. RESOLVING SPECIES BOUNDARIES IN THE AMPHIDINIUM OPERCULATUM SPECIES COMPLEX (DINOPHYCEAE), INCLUDING THE DESCRIPTIONS OF AMPHIDINIUM TRULLA SP. NOV. AND AMPHIDINIUM GIBBOSUM. COMB. NOV.1

Amphidinium operculatum Claparède et Lachmann, the type species of the dinoflagellate genus Amphidinium, has long had an uncertain identity. It has been considered to be either difficult to distinguish from other similar species or a morphologically variable species itself. This has led to the hypothesis that A. operculatum represents a “species complex.” Recently, the problem of distinguishing A. operculatum from similar species has become particularly acute, because several morphologically similar species have been found to produce bioactive compounds of potential interest to the pharmaceutical industry. In this study, we cultured and examined existing cultures of several species of Amphidinium, most of which have been previously identified as A. operculatum or as species considered by some to be synonyms or varieties of A. operculatum. Thirty strains were examined using comparative LM, SEM, and partial large subunit (LSU) rDNA sequence data. Through morphological and molecular phylogenetic analyses, six distinct species were identified, including Amphidinium trulla sp. nov. and Amphidinium gibbosum comb. nov. Amphidinium operculatum was redescribed based on four cultures. Genetic variability within the examined Amphidinium species varied greatly. There was little difference among strains in partial LSU rDNA for most species, but strains of A. carterae and A. massartii Biencheler differed by as much as 4%. In both A. carterae and A. massartii, three distinct genotypes based on partial LSU rDNA were found, but no morphological differences among strains could be observed using LM or SEM. In the case of A. carterae, no biogeographically related molecular differences were found.     

CHROMOSOME NUMBERS IN COMPOSITAE. IV. AMBROSIEAE

New chromosome observations are reported for 30 species and varieties from 4 genera of Ambrosieae: Ambrosia (including Franseria), Diceria, Hymenoclea and Iva. Neither polyploidy nor aneuploidy is known in the genera Dicorea, Hymenoclea or Xanthium. Aneuplcid reduction appears to have played a role in the genome evolution of several species of Iva and Ambrosia. Polyploid species occur in both Iva and Ambrosia and polyploid series exist for at least 5 species or species aggregates of the latter. All available evidence indicates that the primitive chromosome number for the tribe is x = 18, differentiation and speciation having occurred at this level, which is here termed diploid. The group, however, must ultimately have been of polyploid origin from forms with x = 9.     

PALEOZOIC LYCOPSID FRUCTIFICATIONS. I. LEPIDOCARPON PETRIFACTIONS

A reinvestigation of the 4 American species of Lepidocarpon described from petrifactions and of Illiniocarpon cadyi, also described from petrifactions, shows that they are all conspecific. When they, in turn, are compared with specimens of the British petrifaction L. lomaxi, no significant differences can be demonstrated. The criteria cited as diagnostic for the American petrifaction species of Lepidocarpon were found to fail as bases of discrimination when 400 specimens of Lepidocarpon found in coal balls of Pennsylvanian age were studied. Measurements and observations made of a sample size of 136 of these 400 specimens reveal a degree of variation compatible with that of a single species. All previously described American and British petrifaction taxa fall within (or not significantly beyond) this range of variability of a single species as determined from this sample. Additional evidence concerning the 3-dimensional sporophyll structure of this one species of Lepidocarpon and the configurations obtained by certain planes of section through it have served to demonstrate that Illiniocarpon cadyi is in reality a taxon based on sectioned structures of the sporophyll of this Lepidocarpon species. Under the rules of priority, this species of Lepidocarpon and the following are assigned to Lepidocarpon lomaxi: Illiniocarpon cadyi, Lepidocarpon ioense, L. magnificum (megasporangiate form), L. crenatum and L. palmerensis. On the basis of the morphological evidence, the British petrifaction described as Lepidocarpon wildianum is also equated with L. lomaxi.     

Chemotaxonomy of the Hymenophyllaceae. II. C-GLYCOSYLFLAVONES AND FLAVONE-O-GLYCOSIDES OF TRICHOMANES S.L.

An analysis of 23 species of Trichomanes s. 1. indicates that the presence of C-glycosylflavones, especially mono-C-glycosylflavones, may be a basic characteristic for this genus. Except for the morphologically unique Cardiomanes reniforme, this feature appears to delimit the species of Trichomanes s. 1. from those of Hymenophyllum s. 1. Several species, primarily those classified within Didymoglossum (according to both Copeland and Morton), synthesize flavone-O-glycosides in addition to their C-glycosylflavone profiles. Two species, T. birmanicum and T. radicans, appear to be unique in synthesizing the di-C-glycosylflavones violanthin and isoviolanthin; five species (T. collariatum, T. scandins, T. birmanicum, T. bicorne, and T. alatum) appear to synthesize di-C-glycosylflavones but lack mono-C-glycosylflavones. Based on this and other studies, it may be appropriate to consider these C-glycosylflavone-producing plants as representing primitive leptosporangiate stock.     

Sphagnum divinum (sp. nov.) and S. medium Limpr. and their relationship to S. magellanicum Brid.

Sphagnum magellanicum has been viewed as being a predominantly circumpolar species in the northern hemisphere, but it occurs in the southern hemisphere and was originally described from the southern parts of Chile. It is an ecologically important species in mire ecosystems and has been extensively used as a model to study processes of growth, carbon sequestration and peat decomposition. Molecular and experimental studies have, however, revealed genetic structure within S. magellanicum, and morphological differences associated with these genetic groups. Here we describe Sphagnum divinum in Sphagnum subgenus Sphagnum (Sphagnaceae, Bryophyta) as a new species, based on molecular and morphological evidence. Sphagnum medium is reinstated as a distinct species and is epitypified. Consequently, a new species concept of S. magellanicum is presented including an epitypification. Important morphological characters to separate these three species in the field and under the microscope are presented. Ecology and distribution differ among the species; S. divinium has a wide habitat range including mire margin, forested peatlands and moist heaths, and a circumpolar distribution around the northern hemisphere. Sphagnum medium seems to be more restricted to ombrotrophic mire expanse habitats and shows an amphi-Atlantic distribution in the northern hemisphere. Sphagnum magellanicum has a very broad ecological niche in peatlands and is found in most mire habitats in Tierra del Fuego on the southern tip of South America.     

Grosmannia and Leptographium spp. associated with conifer-infesting bark beetles in Finland and Russia, including Leptographium taigense sp. nov.

Species of Grosmannia with Leptographium anamorphs include important forest pathogens and agents of blue stain in timber. They are commonly found in association with forest pests, such as bark beetles. During a survey of ophiostomatoid fungi in eastern parts of Finland and neighboring Russia, species belonging to the genus Grosmannia were isolated from 12 different bark beetle species infesting Picea abies and Pinus sylvestris, the most economically important conifers in the region. Identification of these fungi was based on morphology, DNA sequence comparisons for three gene regions and phylogenetic analyses. A total of ten taxa were identified. These belonged to six different species complexes in Grosmannia. The phylogenetic analyses provided an opportunity to redefine the G. galeiformis-, L. procerum-, L. lundbergii-, G. piceiperda-, G. olivacea- and G. penicillata-complexes, and to consider the species emerging from the survey within the context of these complexes. The species included G. galeiformis, G. olivacea, L. chlamydatum, L. lundbergii, L. truncatum and a novel taxon, described here as L. taigense sp. nov. In addition, species closely related to G. cucullata, G. olivaceapini comb. nov., G. piceiperda and L. procerum were isolated but their identity could not be resolved. The overall results indicate that the diversity of Grosmannia species in the boreal forests remains poorly understood and that further studies are needed to clarify the status of several species or species complexes.     

Chromosomes of Syrphidae. VI. The tribe Pipizini

The karyotypes of 24 species of the tribe Pipisini (Diptera: Syrphidae) are described and illustrated. Nearly all the species of Neocnemodon, Pipiza and Pipizella have 2n=8 chromosomes consisting of a short telocentric XY pair and three metacentric pairs increasing in relative length from long to very long. Pair II chromosomes in several Pipiza species have high metacentric to low submetacentric arm ratios. One Parapenium species is tentatively reported as having five pairs and another five or six pairs. The karyological evidence favours placing the tribe Pipizini in the subfamily Syrphinae rather than in the subfamily Milesiinae.     

GRACILARIOPSIS MCLACHLANII SP. NOV. AND GRACILARIOPSIS PERSICA SP. NOV. OF THE GRACILARIACEAE (GRACILARIALES,RHODOPHYCEAE) FROM THE INDIAN OCEAN1

Two new species of Gracilariopsis from the Indian Ocean are proposed—Gracilariopsis (Gp.) mclachlanii Buriyo, Bellorin et M. C. Oliveira sp. nov. from Tanzania and Gracilariopsis persica Bellorin, Sohrabipour et E. C. Oliveira sp. nov. from Iran—based on morphology and DNA sequence data (rbcL gene and SSU rDNA). Both species fit the typical features of Gracilariopsis: axes cylindrical throughout, freely and loosely ramified up to four orders, with an abrupt transition in cell size from medulla to cortex, cystocarps lacking tubular nutritive cells and superficial spermatangia. Nucleotide sequence comparisons of rbcL and SSU rDNA placed both species into the Gracilariopsis clade as distinct species from all the accepted species for this genus, forming a deeply divergent lineage together with some species from the Pacific. The new species are very difficult to distinguish on morphological grounds from other species of Gracilariopsis, stressing the importance of homologous molecular marker comparisons for the species recognition in this character‐poor genus.     

Three ascomycetes on leaves of evergreen Ilex trees from Japan: Rhytisma ilicis-integrae sp. nov., R. ilicis-latifoliae, and R. ilicis-pedunculosae sp. nov.

Three species belonging to the genus Rhytisma causing tar spot were collected on leaves in evergreen trees of Ilex species from Japan. Rhytisma ilicis-latifoliae, the known species, is found on Ilex latifolia, and R. ilicis-integrae sp. nov. and R. ilicis-pedunculosae sp. nov. are found on I. integra and I. pedunculosa, respectively. Ascomata are formed on the abaxial part of the stromata in all the Rhytisma species studied, and spermogonia are formed on the amphigenous parts in R. ilicis-latifoliae and on the adaxial part in R. ilicis-integrae and R. ilicis-pedunculosae. Shape and size of asci, ascospores, and spermatia are distinctly different among the three species. The morphology of germination tubes from ascospores and appressoria is unique for each Rhytisma species. Yellowish spots arise on the newly developing leaves in mid-May, then abundant spermatia are produced in spermogonia in the three Rhytisma species. In the next year, ascospores are produced in ascomata from early April to late May in R. ilicis-integrae and from early April to early June in R. ilicis-latifoliae and R. ilicis-pedunculosae, and they are considered to be the inocula of disease infection.     

Chassalia magnificens sp. nov. and C. chrysoclada comb. nov. (Rubiaceae) from central Africa

Chassalia magnificens, a new species from the Albertine Rift in eastern Democratic Republic of Congo, is described and illustrated. The species is recognised inter alia by its large stipules and montane habitat. Chassalia chrysoclada is a new combination for a widespread, but hitherto overlooked, central African species originally described in the genus Psychotria. Chassalia chrysoclada is related to C. pteropetala (K. Schum.) Cheek but lacks the bicostate twigs and dorsally winged corolla lobes of that species.     

Amomum dampuianum and A. mizoramense spp. nov. (Zingiberaceae) from Mizoram,northeast India

Two new species of Amomum (Zingiberaceae) from Mizoram are described and illustrated: A. dampuianum and A. mizoramense. Photographs, a comparison with the allied species A. corynostachyum and A. hypoleucum, and a key to the species of Amomum known in Mizoram is also provided.     

Yeasts from U.S.A. soils

Summary Investigations of yeasts from 38 U.S.A. soils samples show the occurrence of 22 different species (16 sporogenous and 6 asporogenous).The most widespread species were Pichia fermentans and Hansenula anomala. The other isolated species were Saccharomyces ellipsoideus, Torulaspora delbrueckii, Pichia membranefaciens, Saccharomyces smittii, Saccharomyces carlsbergensis, Saccharomyces uvarum, Torulaspora rosei, Zygosaccharomyces rouxii, Zygosaccharomyces n. sp., Hansenula saturnus, Hansenula californica, Hansenula n. sp., Hansenula suaveolens, Debaryomyces n. sp., Torulopsis glabrata, Torulopsis n. sp. Candida tropicalis, Candida robusta, Rhodotorula glutinis, Trichosporon cutaneum and Trichosporon cutaneum var. multisporus.