Ciliate Protozoa in the Rumen of Brazilian Water Buffalo,Bubalus bubalis Linnaeus*

SYNOPSIS Total numbers and distribution of genera, subgenera and species were determined for the ciliate protozoa in rumen contents of 4 Brazilian water buffalo Bubalus bubalis Linnaeus. The fauna of one animal, housed in close proximity to European and zebu-type cattle, differed considerably from that of the remaining animals, which were somewhat isolated on a large ranch. Several of the protozoan species observed in the semi-isolated animals were first described in rumen contents from humped Indian cattle, and their subsequent occurrence in other hosts and geographic locations has been limited or absent. In all, 49 different species of protozoa were found, 8 of which have not been previously described. Three of the new species belong to the genus Entodinium: E. ciculum sp. n., E. spinonucleatum sp. n. and E. triangulum sp. n.: 4 to Diplodinium (Ostracodinium): D. (O.) brazili sp. n., D. (O.) esalqum sp. n., D. (O.) nucleolobum sp. n., and D. (O.) tiete sp. n.; and one to Diplodinium (Eudiplodinium): D. (E.) bubalus sp. n.     

John Bishop Duncan

Abstract

Atrichum undulatum (Hedw.) Beauv., Physcomitrium pyriforme (Hedw.) Hampe, Cyclodictyon blumeanum (C. Muell.) O. Kuntze and Tristichella spiculifera Dix., representing four genera of mosses new to Peninsular Malaysia, are reported and the latter two species described and illustrated. Features of ecological and distributional interest are also discussed. The sporophytes of Tristichella spiculifera are described and figured for the first time.     

A new check-list of the mosses of Turkey

Abstract

The check-list includes a list of genera, species, subspecies and varieties of Turkish mosses. It is composed of 726 species, subspecies and varieties representing 164 genera and 42 families. Accompanying the lists are a systematic arrangement of the genera, species and varieties and lists of synonyms, excluded species and of annotations. Three mosses, Pseudoleskeella rupestris (Berggr.) Hedenäs & L. Söderstr., Isothecium myosuroides Brid. var. brachythecioides (Dixon) C.E.O. Jensen, Eurhynchium hians (Hedw.) Sande. Lac. var. rigidum (Boulay) J.-P. Frahm are recorded as new for the moss flora of Turkey.     

Oxytropis sobolevskajae sp. nov. (Fabaceae: Papilionoideae,Galegeae) from Tuva Republic (south Siberia,Russia)

Oxytropis sobolevskajae Pjak, a new species endemic to Tuva Republic (south Siberia, Russia), is described and illustrated. The new species belongs to O. sect. Xerobia Bunge subsect. Ampulla Vass. and is confined to the central Tuva depression. This species is probably most closely related to O. leptophylla (Pall.) DC., from which it is easily distinguished by the number of leaflet pairs, the length and type of inflorescence, and the length of the keel cusp.     

A new species of <Emphasis Type="Italic">Eurycletodes</Emphasis> Sars, 1909 (Copepoda: Harpacticoida: Argestidae) from the southern hemisphere including remarks on the phylogeny of the genus and its subgenera

This paper deals with taxonomy and phylogenetics of the genus Eurycletodes Sars, 1909 (Copepoda: Harpacticoida: Argestidae). Samples, collected from the southeast Atlantic on board RV “Meteor” during the cruises DIVA-1 (M48/1) and DIVA-2 (M63/2), contain specimens of Eurycletodes. Eurycletodes is characterized as a monophylum by A1 segments III + IV fused, basal seta of md palp lost, exp of md palp reduced to 1 seta or completely lost. Similarly, the subgenera Eurycletodes (Eurycletodes) and Eurycletodes (Oligocletodes) are characterized as monophyletic by the loss of the inner seta on P1 exp2 (apomorphic to E. (E.)) and the absence of the inner seta on P5 endopodal lobe (apomorphic to E. (O.)). Eurycletodes profundus is renamed as E. (O.) profundus. Eurycletodes ephippiger is the only species of the genus without subgeneric designation. Eurycletodes (O.) diva sp. nov. is described. The new species differs from described species of the genus by a larger body size, P5 endopodal lobe only slightly protruding, last segment of A1 with 2 outer setae, furcal rami elongated between setae VII and IV. The occurrence of 2 specimens of Eurycletodes (O.) diva sp. nov. at 2 sites separated by the Walvis Ridge supports the hypothesis that geographic obstacles do not prevent harpacticoid copepods from spreading in the deep sea.     

A new skink species (Oligosoma taumakae sp. nov.; Reptilia: Scincidae) from the Open Bay Islands,New Zealand

Abstract

We describe a new skink species (Oligosoma taumakae sp. nov.) from the Open Bay Islands, New Zealand. This species is diagnosed on the basis of several morphological characteristics, and its specific status is supported by mitochondrial sequence data (ND2, ND4). The new species appears to be most closely related to O. acrinasum, O. infra‐punctatum, O. otagense and O. waimatense. The new taxon appears to be rare and endemic to the island of Taumaka in the Open Bay Islands (off the west coast of the South Island). Predation by a flightless rail (weka, Gallirallus australis), native to New Zealand but introduced to the Open Bay Islands, is a major conservation concern.     

The families of bitunicate ascomycetes

The morphology and nomenclature of ca. 195 families of bitunicate or alleged bitunicate ascomycetes are discussed. Available representatives of these families were studied especially with respect to the morphology of the asci and ascospores. The morphology of the ascomata, etc. was studied in the SEM in 73 species. The following morphological terms are introduced: hamathecium, pseudoprototunicate, pseudofis–situnicate, semifissitunicate, and umbilicus. The following taxa are described as new: Coccodiniaceae O. Erikss. fam. nov., Microtheliopsidaceae O. Erikss. fam. nov., Amarenomyces O. Erikss. gen. nov., and Euantennaria abietina O. Erikss. sp. nov. The name Lecanidiaceae is proposed to replace Patellariaceae Corda, and Cyanoder–mella to replace Cyanoderma Höhn. The Massariaceae are treated as Trypetheliaceae subfam. Massarioideae (Nits.) O. Erikss. The following new combinations are proposed: Amarenomyces ammophilae (Lasch) O. Erikss., Cyanodermella viridula (Berk. & Curt.) O. Erikss., C. Candida (Setch.) O. Erikss., Dictyotrichiella delicatula (Ves–tergr.) O. Erikss., Laurera sepulta (Mont.) O. Erikss., Splanchnonema superans (Mull. Arg.) O. Erikss. and Thelenella antarctica (M. Lamb) O. Erikss. The origin and evolution of the Ascomycetes are discussed, and the importance of paedomor–phosis in the transspeciation of the group is emphasized. The stratigraphic classification of the Ascomycetes is discussed. In a transitional classification of the Ascomycetes, 109 monophyletic entities (clades) are recognized. La morphologie et la nomenclature ?environ 195 families ?ascomycétes bituniques ou soit–disant bituniques sont étudiées, spécialement en respectant la morphologie des asques et des ascospores. La morphologie des ascocarpes, etc. de 73 espèces fut étudiée dans le SEM. Les termes morphologiques suivants sont introduits: hamathecium, pseudoprototunique, pseudofissitunique, semifissitunique et umbilicus. Ces nouveaux taxa sont decrits: Coccodiniaceae O. Erikss. fam. nov., Microtheliopsidaceae O. Erikss. fam. nov., Amarenomyces O. Erikss. gen. nov. et Euantennaria abietina O. Erikss. sp. nov. Le nom Lecanidiaceae est proposéà la place de Patellariaceae Corda, Cyanodermella à la place de Cyanoderma Höhn. Les Massariaceae sont traitées comme Trypetheliaceae subfam. Massarioideae (Nits.) O. Erikss. Les nouvelles combinations suivantes sont proposées: Amarenomyces ammophilae (Lasch) O. Erikss., Cyanodermella viridula (Berk. & Curt.) O. Erikss., C. Candida (Setch.) O. Erikss., Dictyotrichiella delicatula (Vestergr.) O. Erikss., Laurera sepulta (Mont.) O. Erikss., Splanchnonema superans (Müll. Arg.) O. Erikss. et Thelenella antarctica (M. Lamb) O. Erikss. ?origine et ?évolution des ascomycètes sont discutées, et I'importance de la paedomorphose dans la transspeciation du groupe est mise en évidence. La classification stratigraphique des ascomycètes est discutée. Dans une classification de transition des ascomycètes, 109 entités monophyletiques sont reconnues.     

Einige für die bulgarische Flora neue und seltene Arten

The author reports new for the science and new and rare plants species for the Bulgarian Flora. The new species for the science are Ranunculus stojanovii sp. nov. and Ophioglossum vulgatum L. var. ovatum var. nov. R. stojanovii grow wild near Ravnogor village, Pazardžik district (Rhodopi mountain at 1200 m.s.l.). O. vulgatum L. var. ovatum is collected in the meadows at Banja village near by Karlovo town, Plovdiv district. The new species for the Bulgarian Flora are Erythronium dens-canis L. ssp. niveum (Baumg.) Buia et Paun, collected at Radovci village, Tarnovo district, and Parentucellia latifolia L. f. albiflora (Raul) Hall, collected at Banja village, Plovdiv district. The remaining 21 species are rare for the Bulgarian Flora. New localities are indicated for them.     

Orthotrichum dentatum T.Kiebacher & Lüth sp. nov. (Orthotrichaceae)

A new species of Orthotrichum, O. dentatum T.Kiebacher & Lüth, is described from the European Alps. The new species belongs to the subgenus Pulchella (Schimp.) Vitt, section Diaphana Vent. Orthotrichum dentatum is similar to O. schimperi Hammar but differs from the latter in that it features a hairy calyptra, denticulate to dentate leaf apices and strongly keeled leaves. Orthotrichum dentatum grows as an epiphyte on a variety of deciduous trees. So far, the new species has only been found in Italy and Switzerland.     

Ophiostoma novo-ulmi sp. nov., causative agent of current Dutch elm disease pandemics

The aggressive subgroup of the Dutch elm disease pathogen Ophiostoma ulmi (Buism.) Nannf. syn. Ceratocystis ulmi (Buism.) Moreau is named as a new species, O. novo-ulmi, and is thereby separated from the old non-aggressive subgroup, which is retained as O. ulmi. O. novo-ulmi differs from O. ulmi in colony morphology, growth rate, optimum temperature for growth, perithecial neck length, pathogenicity to elm, bark colonising ability, cerato-ulmin protein production, synnemetal and protoperithecial production, mating type frequency, protein and isozyme polymorphisms, mitochondrial DNA and nuclear DNA polymorphisms, and mitochondrial DNA size. In addition, a strong unidirectional fertility barrier operates between the two species, while their hybrids show remarkable variation, poor fitness, and many are infertile. These aspects are summarised. New information on perithecial dimensions is presented. O. ulmi is redefined and a neotype designated. The status of the Eurasian and North American races of O. novo-ulmi is currently under investigation.Abbreviations EAN Eurasian race - NAN North American race     

A new classification for the subgenera of the genus Acanthophthirius Perkins,with descriptions of twelve new taxa (Acarina,Trombidiformes, Myobiidae)

The myobiid genus Acanthophthirius Perkins, to date comprising four subgenera, is reviewed and divided into just two subgenera, the nominate subgenus and Myotimyobia Fain. The male genital shield and female opisthogastric sclerites, which are here considered to be part of female genitalia, are adopted as the criteria for dividing the subgenera. These structures are essentially the same in form and position in the subgenus Acanthopthirius in its revised sense, while they are both more heterogeneous in species of the redefined subgenus Myotimyobia. The subgenera Acanthophthirius Fain and Chiromyobia Fain are thought to represent species-groups in the nominate subgenus, named respectively the etheldredae and miniopteri groups. The following one new subspecies and 11 new species are described: A. (A.) womersleyi eptesicus, A. (A.) glauconycteris, A. (A.) mauritaniensis, A. (A.) philetoris, A. (A.) otonycteris, A. (A.) steatocaudatus, A. (A.) nyctophilis, A. (M.) vagus, A. (M.) longus A. (M.) baueris, A. (A.) hesperopteris (female only) and A. (M.) pixonixeos (female only). A. (M.) hanensis is synonymised with A. (M.) namurensis, and A. (M.) capacini is emended to A. (M.) capaccinii and relegated to a subspecies of A. (M.) myotis. All the known and new species are assigned to their respective subgenera and shown in a table. Incongruent host-relationships of some of the mites are clarified, although not completely solved, by the introduction of the new classification for the subgenera.     

中国棘豆属（豆科）二新记录种

报道了中国棘豆属二新记录种——黄绿花棘豆和丛棘豆。黄绿花棘豆主要分布于蒙古国,丛棘豆主要分布于蒙古国和俄罗斯,在中国为首次记录。文中凭证标本存放于内蒙古大学植物标本馆(HIMC)。     

A review of chromosome cytology in Hyacinthaceae subfamily Ornithogaloideae (Albuca, Dipcadi, Ornithogalum and Pseudogaltonia) in sub-Saharan Africa

The chromosome cytology of Hyacinthaceae subfamily Ornithogaloideae is reviewed within the framework of a recent molecular-based classification, with particular emphasis on its center of diversity in sub-Saharan Africa. We also provide new chromosome counts for sections that are unknown or poorly known cytologically. Albuca subgen. Namibiogalum (9 spp.) probably has an ancestral base number of x = 10 but subgen. Albuca (± 70 spp), subgen. Monarchos (9 spp.) and subgen. Osmyne (36 spp.) have x = 9. The pattern in subgen. Urophyllon (3 spp.) is remarkable: although x = 6 is likely, the species in the section exhibit a range of 2n = 12, 10, 8, 6 and 4 (exclusive of polyploidy). All karyotypes have three large chromosome pairs and a variable number of small chromosomes. Pseudogaltonia (2 spp.) has x = 9 and Dipcadi (26 spp.) possibly x = 9 in series Uropetalum and x = 6 in series Dipcadi, which exhibits a pattern of descending dysploidy leading to n = 3 in D. marlothii. In Ornithogalum (± 130 spp.) chromosome numbers are known for only 24 of the ± 84 sub-Saharan species, mostly from subgen. Aspasia and subgen. Ornithogalum sect. Linaspasia, both of which have x = 6, and from subgen. Galtonia, which has x = 8. In contrast, x = 7 is basic for the Eurasian sects. Honorius and Melophis, and x = 18 seems likely for sect. Cathissa. Sect. Ornithogalum, the cytology of which we does not examine in detail, may have x = 9. Polyploidy is apparently rare in the sub-Saharan African ornithogaloids, in marked contrast to the high frequency of polyploidy among Eurasian species. In Albuca just 3 or possibly 4 sub-Saharan species (9% or 13% of those counted) are exclusively polyploid and 5 more have diploid and polyploid races; and in sub-Saharan Ornithogalum, only the tropical O. gracillimum is exclusively polyploid, and the western southern African O. hispidum has diploid and polyploid races.     

Acceptance and suitability of novel trees for <Emphasis Type="Italic">Orthotomicus erosus</Emphasis>, an exotic bark beetle in North America

To predict whether an herbivorous pest insect will establish in a new area, the potential host plants must be known. For invading bark beetles, adults must recognize and accept trees suitable for larval development. The preference-performance hypothesis predicts that adults will select host species that maximize the fitness of their offspring. We tested five species of North American conifers and one angiosperm for adult acceptance and suitability for reproduction of the Mediterranean pine engraver, Orthotomicus erosus (Wollaston). Red pine, Pinus resinosa Aiton, and white spruce, Picea glauca (Moench) Voss, were accepted by adult beetles and suitable for reproduction to the extent of adult replacement. Others, such as balsam fir, Abies balsamea (L.) Mill., eastern hemlock, Tsuga canagensis (L.) Carrière, and tamarack, Larix laricina (Du Roi) Koch, were acceptable but unsuitable. The presence of tree species that are acceptable to adults but unsuitable for reproduction may affect the ability of O. erosus to establish across North America.     

El género Ochrolechia A. Massai. (Pertusariaceae,liquenes) en Espana y Portugal

The genus Ochrolechia is widespread in Spain and Portugal and now includes 14 species, 1 form and 4 chemical races (11 species and 3 chemical races are epiphytes, 2 species, 1 form and 1 chemical race are saxicolous and one species is muscicolous). We propose a new combination: O. dalmatica (Erichsen) Boqueras. Eight species are excluded from the Spanish and Portuguese floras: O. aggregata (Bagl.) Verseghy, O. anomala Verseghy, O. glaucescens (Hue) Zahlbr., O.frigida (Sw.) Lynge, O. pseudotartarea (Vain.) Verseghy, O. rosella Müll. Arg., O. subpallescens Verseghy, O. tenuissima Verseghy, O. crozalsiana Clauzade et Vêzda is included in O. tartarea. The criteria for the identification of these species are: 1 ) the chemical substances (the presence/absence of gyrophoric acid in the thallus and/or in the apothecia determines the groups inside of the genus, the presence of alectoronic acid determines the chemical races); 2) thallus with or without soredia or isidia; 3) the presence of pruina on the disc; and 4) the substratum. A key for the identification to all mentioned species is included.     

A new species of Cardamine subgen. Dentaria (Cruciferae), apoendemic in Calabria (Southern Italy)

ABSTRACT

Cardamine battagliae Cesca & Peruzzi sp. nova is related to Cardamine heptaphylla (Vill.) O. E. Schulz. (2n = 48). On the other hand, the new species is well distinguished both from a morphological and karyological point of view. Because of its distribution and high ploidy level (2n = ca. 160) C. battagliae can be considered as a new apoendemic taxon. Morphological and karyological data are presented and discussed.     

On two new species of Oswaldella Stechow, 1919 (Cnidaria, Hydrozoa) from Bransfield Strait (Antarctica)

Two species of the genus Oswaldella Stechow, 1919 new to science (Oswaldella crassa sp. nov. and O.␣curiosa sp. nov.) were studied. Both species are described and figured; their systematic position amongst the remaining species of the genus is discussed. The material originates from the Bransfield Strait area (Antarctica) and was collected during the United States Antarctic Research Program with R.V. Eltanin. A comparative table listing the main features of the known species of Oswaldella is presented. Finally, a general survey of geographical and bathymetrical distribution of the known species of Oswaldella is given. Received: 8 October 1997 / Accepted: 2 February 1998