Chromosome counts of some Cuban Angiosperms

Chromosome numbers are reported for 14 species collected in Cuba. The first chromosome records are reported forAlbizzia cubana Britton etWilson (2n=26),Atkinsia cubensis (Britton etWilson)Howard (2n=26),Caesalpinia violacea (Mill.)Standl. (2n=24),Colubrina ferruginosa Brongn. (2n=24). Chromosome numbers of the following species were confirmed:Albizzia lebbeck (L.)Benth. (2n=26),Canavalia maritima (Aubl.)Thouars (2n=22),Casuarina equisetifolia Forst. (2n=18),Cedrela mexicana M.J. Roem. (2n=56),Delonix regia (Bojer)Raf. (2n=28),Guazuma tomentosa H.B.K. (2n=16),Lysiloma bahamense Benth. (2n=26),L. latisiliqua (L.)Benth. (2n=26),Samanea saman (Jacq.)Merrill (2n=26),Thespesia populnea (L.)Soland (2n=26).     

A revision ofTaraxacum sect.Piesis (Compositae)

On the basis of allozyme and cultivation data, and of additional herbarium material, a taxonomic and nomenclatural revision ofTaraxacum sect.Piesis A.J. Richards exKirschner et?těpánek is provided. The section is made up of halophilous, sexually reproducing taxa. InT. stenocephalum Boiss. etKotschy,T. pindicum Kirschner et?těpánek, sp. nov., andT. perenne Kirschner et?těpánek, sp. nov., a tetraploid chromosome number has been recorded, representing the only known case of sexuality at the tetraploid level in the genus. The complex ofT. stenocephalum, includes some geographically and morphologically extreme populations treated as subspecies: subsp.gumusanicum (Soest)Kirschner et?těpánek, comb. nov., subsp.magnum Kirschner et?těpánek, subsp. nov., and subsp.daralagesicum (Schischk.)Kirschner et?těpánek, comb. nov. In addition toT. bessarabicum (Hornem.)Hand.-Mazz., a widely distributed Eurasian species,T. stenocephalum, a complex centred in Transcaucasia and Anatolia, andT. pachypodum H. Lindb., a North African endemic, four new species are described:T. salsum Kirschner et?těpánek, sp. nov., a diploid endemic confined to E Crimea,T. perenne Kirschner et?těpánek, sp. nov., a tetraploid sexual species known only from SW Crimea,T. pindicum Kirschner et?těpánek, sp. nov., a remarkable tetraploid endemic to the Pindos Mts., Greece, andT. salsitatis Kirschner, ?těpänek etYirdirimli, sp. nov., an Anatolian diploid species. Furthermore, a hybrid betweenT. salsum andT. bessarabicum from Crimea (documented on the basis of allozyme data elsewhere) is given a binomial,T. xmesohalobium Kirschner et?těpánek, nothosp. nov.     

Notes on some African hepatic genera 1–5

The present study deals with five genera of hepatics in Africa, Isotachis Mitt., Anastrophyllum (Spruce) Steph., Tritomaria Schiffn. ex Loeske, Gymnocoleopsis (Schust.) Schust. and Lophozia (Dum.) Dum. All African populations of the genus Isotachis Mitt. are considered to be one species, I. aubertii (Schwaegr.) Mitt. Four species of Anastrophyllum (Spruce) Steph. (s.l.), A. auritum (Lehm.) Steph., A. piligerum (Nees) Spruce, A. subcomplicatum (Lehm. et Lindenb.) Steph. and A. minutum (Schreb.) Schust., and two species of Tritomaria Schiffn. et Loeske, T. camerunensis S. Arnell and T. exsecta (Schrad.) Schiffn. ex Loeske occur in Africa. Gymmocoleopsis multiflora (Steph.) Schust. represents a genus and species hitherto unreported for the African flora. Finally, five Lophozia (Dum.) Dum. species, L. argentina (Steph.) Schust., L. capensis S. Arnell, L. decolorans (Limpr.) Steph., L. hedbergii S. Arnell and L. tristaniana (S. Arnell) Váňa, are reported from central and southern Africa; two of these (L. argentina (Steph.) Schust. and L. decolorans (Limpr.) Steph.) represent the first reports from Africa.     

Bucania (Gastropoda) from the Ordovician of Estonia

Seven species ofBucania Hall 1847 from the Ordovician of Estonia are presented, also taking into consideration Pleistocene drift material from Germany, and their stratigraphical and geographical distributions are revised. The Middle Ordovician speciesBucania latissima Koken 1897 andBucania salpinx Koken 1897 are tentatively assigned toMegalomphala Ulrich inUlrich &Scofield 1897, while the Lower Ordovician speciesBucania macera Koken inKoken &Perner 1925 is placed inSalpingostoma Roemer 1876. The Middle OrdovicianBucania czekanowskii (Schmidt 1858) and the Upper OrdovicianBucania radiata (d’Eichwald 1856) were earlier considered conspecific, but based on study of the type material they are here considered distinct species.Salpingostoma cornu (Koken 1897), commonly referred to this genus because of the trema, is here transferred toBucania. Two Upper Ordovician specimens ofBucania display wide and abruptly flaring apertures morphologically far removed from other species of the genus.     

Annotated chromosome numbers of selected asiaticPotentilla species

Chromosome numbers are reported for 19 collections representing 16 AsiaticPotentilla taxa. The first chromosome records are reported forP. desertorum Bunge var.arnavatensis Wolf (2n=28),P. festiva Soják (2n=28),P. griffithii Hook f. subsp.beauvaisii (Cardot) Soják (2n=42),P. micropetala D. Don subsp.byssitecta (Soják) Měsí?ek etSoják (2n=14),P. mollissima Lehm. (2n=28),P. moorcroftii Wall. exLehm. (2n=42),P. multicaulis Bunge (2n=14),P. [x]omissa Soják (2n=35, 56, 70) andP. stanjukoviczii Ovcz. exKoczk. (2n=14). Counts differing from those previously recorded are given forP. algida Soják (2n=56) andP. flagellaris Willd. exSchlecht. (2n=42). Chromosome numbers of the following species were confirmed:P. [x]agrimonioides Bieb. (2n=42),P. chinensis Ser. in DC. (2n=14),P. fragarioides L. (2n=14),P. lineata Trev. (2n=14) andP. sericea L. (2n=28). Taxonomy is briefly discussed. A new combinationP. micropetala D. Don subsp.byssitecta (Soják) Měsí?ek etSoják stat. nov. is proposed.     

Chromosome numbers in selectedHieracium species in the Krkonoše Mts. (the West Sudeten)

Chromosome numbers are given of 15 species of the genusHieracium L. s. str., representing seven species groups (in the sense of Flora Europaea, roughly corresponding to Zahn's “species principales”) from the Krkono?e Mts., N. Bohemia and SW Poland. For the first time chromosome numbers are reported forH. melanocephalum Tausch (2n=27),H. tubulosum Tausch (2n=36),H. schustleri Zlatník (2n=36),H. fritzei F. Schultz (2n=27),H. rohlenae Zlatník (2n=27),H. nigrescens Willd. (2n=36),H. decipiens Tausch (2n=36),H. atrellum Juxip inSchischkin etBobrov (2n=27),H. subnigrescens (Fries exNorrlin)Dahlst. (2n=36),H. sudeticum Sternberg (2n=36),H. pedunculare Tausch (2n=36),H. glandulosodentatum Uechtr. (2n=36),H. wimmeri Uechtr. (2n=27). InHieracium alpinum L. s. str. the number 2n=27 has been confirmed. The results show a high proportion of tetraploid taxa; no diploids have been found.     

Lower Cambrian tubular micro-to macrofossils from the Paseky Shale of the Barrandian area (Czech Republic)

The carbonaceous megafossil (mega-alga)Marpolia spissa Walcott 1919 is described from the Early Cambrian of the Barrandian area for the first time. Macroscopic remains of colonies ofM. spissa are compared with tubular microfossils of the same rocks. Different areas in colonies ofM. spissa are assignable to several (part-based) genera and species of microfossils. Therefore, the microfossil taxaSiphonophycus robustum (Schopf 1968)Knoll et al. 1991,S. typicum (Hermann 1974)Butterfield 1994,S. kestron Schopf 1968,S. capitaneum Nyberg &Schopf 1984,Polytrichoides lineatus Hermann 1974, emend.Knoll et al. 1991,Tortunema angusta (Kolosov 1984)Butterfield 1994 andTortunema wernadskii (Schepeleva 1960)Butterfield 1994 should only be used as form-species in the sense of an artificial taxonomy. The palaeoenvironment of the Paseky Shale and the biological assignment ofMarpolia spissa are discussed.     

Chromosome counts and chromosome morphology of some selected species

In the years 1976–1981 we studied chromosome counts and karyotypic formulae of the following 29 species of plants from 41 localities (of these 6 from Bohemia, 32 from Moravia, 3 from Slovakia):Batrachium baudotii (Godron) F. W. Schultz,Chenopodium rubrum L.,C. polyspermum L.,C. murale L.,C. ficifolium Sm.,C. opulifolium Schrader ex DC. inLam. et DC.,C. strictum Roth [subsp.strictum, subsp.glaucophyllum (Aellen)Aellen inJust etAellen, subsp.striatiforme Uotila],Arenaria grandiflora L.,Illecebrum verticillatum L.,Spergula morisonii Boreau inDuchartre,Spergularia marginata (DC. inLam. et DC.)Kittel S. marina (L.)Griseb.,S. rubra (L.) J. etC. Presl,Silene conica L.,Sisymbrium loeselii L.,S. volgense Bieb. exE. Fourn.,S. orientale L. [subsp. orientale, subsp.macroloma (A. Pomel)Dvo?ák],S. officinale (L.)Scop.,Descurainia sophia (L.)Webb exPrantl inEngler etPrantl,Nasturtium officinale R. Br. inAiton,Barbarea arcuata (Opiz inPresl J. et C.)Reichenb.,Lunaria annua L.,Soldanella montana Willd.,S. carpatica Vierh. inUrban etGraebner,Lotus tenuis Waldst. etKit. exWilld.,L. uliginosus Schkuhr,Trigonella monspeliaca L.,Geranium sibiricum L.,Lactuca tatarica (L.)C. A. Meyer.     

Chromosome numbers in Czechoslovak species ofGagea (Liliaceae)

Chromosome numbers are reported for the following Czechoslovak representatives of the genusGagea Salisb.:G. bohemica (Zauschn.) J. A. etJ. H. Schult. subsp.bohemica (2n=60),G. lutea (L.)Ker-Gawl. (2n=72),G. minima (L.)Ker-Gawl. (2n=24),G. cf.paczoskii (Zapal.) Grossh. (2n=48),G. cf.pomeranica Ruthe (2n=48),G. pratensis (Pers.) Dum. s. str. (2n=60),G. pusilla (F. W. Schmidt) J. A. etJ. H. Schult. (2n=24),G. spathacea (Hayne) Salisb. (2n=106), andG. villosa (M. Bieb.) Duby (2n=48). Meiotic behavior was found to be essentially regular inG. pusilla andG. villosa whereas a high proportion of meiotic irregularities was noted inG. bohemica andG. pratensis s. str.     

Polyploidy and variation in theCampanula rotundifolia complex. Part II. (Taxonomic) I. Revision of the groupsSaxicolae,Lanceolatae andAlpicolae in Czechoslovakia and adjacent regions

A survey is given of three natural groups of the subsectionHeterophylla (Witas.)Fed. of the genusCampanula L. Within theSaxicolae four taxa of higher rank have been revealed:c. xylocarpa Kovanda (2n=34),C. gentilis Kovanda (2n=34),C. moravica (Spitzner)Kovanda subsp.moravica (2n=68), andC. moravica subsp.xylorrhiza (O. Schwarz)Kovanda (2n=102). BothAlpicolae andLanceolatae are represented by a single species: the first byC. cochleariifolia Lam. (2n=34), the latter byC. serrata (Kit. ap.Schult.)Hendrych (2n=34). Cytology, ecology and geographical distribution of all these taxa have been reviewed, and relationships to the other members of the complex discussed. Infraspecific variation within each species has also been examined.     

Notes on the genusOenothera subsect.Oenothera (Onagraceae) in the Czech Republic

Up-to-date results of taxonomic and phytogeographic studies ofOenothera subsect.Oenothera in the eastern part of the Czech Republic (Moravia and Silesia) are presented. A new hybridogenous species,Oe. moravica Jehlík etRostański (=Oe. fallax × Oe. victorini), is described from S Moravia. Several taxa and hybrids are reported for the first time for the Czech Republic:Oe. victorini Gates etCatcheside (=Oe. rostanskii Jehlík),Oe. × wienii Renner exRostański,Oe. acutifolia × Oe. victorini. Other taxa are recorded from the eastern part of the Czech Republic for the first time:Oe. acutifolia Rostański,Oe. hoelscheri Renner exRostański,Oe. parviflora L.,Oe. subterminalis Gates. The taxonomy ofOe. pycnocarpa Atkinson etBartlett is discussed. A survey of species and hybrids ofOenothera subsect.Oenothera in the Czech Republic is added.     

Studien über dieJungermannioideae (Hepaticae) 6.Jungermannia Subg.Solenostoma: Europäische und nordamerikanische Arten

Dersechste Beitrag aus der Serie der vorbereiteten Studien über die SubfamilieJungermannioideae (Jungermanniaceae, Hepaticae) enthält die taxonomische Bearbeitung des Subg.Solenostoma (Mitt.)Amak. (GattungJungermannia L. emend.Dum.) in Europa (inkl. Kaukasus und Kleinasien) und Nordamerika. Im genannten Gebiet kommen 10 Arten vor, u. zw.J. caespiticia Lindenb.,J. caucasica Váňa,J. confertissima Nees,J. gracillima Sm.,J. handelii (Schiffn.)Amak.,J. jenseniana Grolle,J. lignicola (Schiffn.)Grolle,J. pyriflora Steph.,J. rubra Gott. exUnd. undJ. sphaerocarpa Hook. Die ArtJ. confertissima Nees (bisher alsSolenostoma levieri (Steph.)Steph. bezeichnet) gehört zu der SektionDesmorhiza Amak., alle anderen Arten gehören zu der SektionSolenostoma.     

Draba skrivanekii,eine interessante Art aus Montenegro (Jugoslawien)

In den Herbarien der botanischen Abteilung des Nationalmuseums in Pr?honice (PR) werden zwei Belege aufbewahrt, die vonRohlena alsDraba athoa Boiss. bezeichnet sind. Später ordneteRohlena selbst diese Pflanzen der ArtD. elongata Host mit Bezeichnung var.skrivanekii Rohl. zu. Durch eine Analyse des Herbarmaterials hat sich erwiesen, dass es sich um eine selbständige Art—Draba skrivanekii (Rohl.)Chrtek—handelt, die in den Gebirgslagen Montenegros (Kom Vasojevi?ki) wahrscheinlich endemisch ist. Die nächstverwandte Art istDraba athoa (Griseb.)Boiss.     

Studien über dieJungermannioideae (Hepaticae) 10.Nardia

Die vorliegende Studie, die letzte aus der Serie der vorbereiteten, Studien über die SubfamilieJungermannioideue (Jungermanniaceae, Hepaticae) ist den Arten der GattungNardia S. Gray corr.Carring. gewidmet. Die GattungNardia wird in zwei Untergattungen gegliedert, u. zw. Subg.Geoscypharia Trev. mit den Sektionen Sect.Breidlerion Grolle (2 Arten), Sect.Flagelliformes Inoue (2 Arten), Sect.Geoscypharia (6 Arten), Sect.Nudae sect. nova (1 Art) und Sect.Subclavatae Inoue (3 Arten) und Subg.Nardia (1 Art). Von 16 bekannten Arten der Gattung (eine Art, die nur im sterilen Zustand bekannt ist, hat eine unsichere Stellung) sind in dieser Studie 8 Arten (N. breidleri (Limpr.) Lindb.,N. geoscyphus (De Not.) Lindb.,N. insecta Lindb.,N. scalaris S. Gray corr. Trev.,N. nuda (Lindenb. etGott.)Váňa,N. assamica (Mitt.) Amak.,N. succulenta (Rich. exLehm.)Spruce undN. compressa (Hook.) S. Gray corr. Trev.) eingehend taxonomisch bearbeitet. Die verbliebenen 8 Arten wurden schon von anderen Autoren (Amakawa, Grolle, Inoue, Schuster) oder vom Verfasser in früheren Studien bearbeitet.     

New chromosome counts in nine endemic species from Iran

Original meiotic chromosome counts are presented for nine endemic species in seven families of Angiosperms from Iran including:Arum giganteum Ghahr. (Araceae) (n=14),Caccinia actinobole Bunge (Boraginaceae) (n=8),Delphinium aquilegifolium (Boiss.)Bornm. (Ranunculaceae) (n=8),Diplotaenia damavandica Mozaff., Hedge etLamond (Apiaceae) (n=11),Gypsophila caricifolia Boiss. (Caryophyllaceae) (n=17),Iphiona arachnoidea (Boiss.)Anderb. (Asteraceae) (n=9),Moltkia gypsacea Rech. f. etAellen (Boraginaceae) (n=20),Onobrychis gaubae Bornm. (Fabaceae) (n=8) andOnosma platyphyllum Riedl (Boraginaceae) (n=9). Eight counts are reported for the first time. Furthermore, the previous chromosome count forIphiona aracnoidea is corrected. Based on cytological data the species status ofMoltkia gypsacea is confirmed; it is not merely synonymous withM. coerulea (Willd.)Lehm. The basic chromosome number n=11 is reported in the genusDiplotaenia for the first time.     

Contribution to the knowledge ofEchinodorus macrophyllus (Kunth)Mich. andE. scaber Rataj from tropical America

The paper deals with the taxonomy and geographical distribution of the two species of the genusEchinodorus whichFassett (1955) did not work up satisfactorily in his revision i.e.Echinodorus macrophyllus (Kunth)Mich. whichFassett does not quote at all, andE. scaber Rataj whichFassett mistook forE. muricatus Griseb. Further a new variety and the diagnoses of hybrids, among whichE. punctatus Mich. is included, are cited.     

The systematic significance of seed morphology and anatomy in thePortulacaceae (Centrospermae)

Nyananyo B. L. (1988): The systematic significance of seed morphology and anatomy in thePortulacaceae (Centrospermae).—Folia Geobot. Phytotax., Praha, 23: 275–279.—The seeds of 115 species in eighteen genera of the familyPortulacaceae were examined with the scanning electron microscope. Longitudinal sections of seeds of representatives of all the genera were examined with the light microscope. Two broad groups based on shape of the seeds, ornamentation of the external surface of their testa, and the position of the embryo relative to the endosperm were recognised. The first group comprising three genera:Anacampseros L.,Grahamia Gillies andTalinopsis A. Gray, have seeds which are pyriform with wings and trichomes, and an embryo that is more or less parallel to the endosperm, while the second of fifteen genera:Calandrinia H.B.K.,Calyptridium Nuttall,Calyptrotheca Gilg,Ceraria Pearson etStephens,Claytonia L.,Lenzia Philippi,Lewisia Pursh,Lyallia Hooker fil.,Montia L.,Portulaca L.,Portulacaria Jacquin,Silvaea Philippi,Talinella Baillon,Talinum Adanson, andWangerinia Franz, are reniform without wings and with an embryo that is horse-shoe shaped around the endosperm.     

Ein Beitrag zur Nomenklatur sphinctozoider Schwämme (Porifera)

The sphinctozoid sponge generaFania Senowbari-Daryan 1990 andSpica Termier &Termier 1977 are preoccupied.Fania is replaced byFanthalamia nom. nov. andSpica by the younger synonymFistulispongia Termier &Termier 1977. The invalid subfamily name FaniinaeSenowbari-Daryan 1990 is replaced by Fanthalamiinae n. subfam. The invalid family and subfamily names SpicidaeTermier &Termier 1977 and SpicinaeSenowbari-Daryan 1990 respectively are replaced by FistulispongiidaeTermier atTermier 1977 and FistulispongiinaeSenowbari-Daryan 1990. The generaWaagenium de Laubenfels 1957 andCatubria Merla 1931 were previously overlooked.Waagenium DeLaubenfels 1957 is a younger synonym ofColospongia Laube 1865. The position ofCatubria Merla 1931 is uncertain. Most probablyCatubria is an alga.