Die GattungAdelocaryum Brand

Summary Adelocaryum anchusoides (Lindl.)Brand andA. capusii (Franch.)Brand are members of the genusLindelofia,A. Schlagintweitii Brand,A. erythraeum Brand,A. flexuosum Brand undA. malabaricum (C. B.Clarke)Brand are newly combined toCynoglossum, A. coelestinum (Lindl.)Brand is a species of subgenusEleutherostylum inCynoglossum in which genus it had already been placed byLindley.     

The genusAntennaria (Asteraceae: Inuleae) in western North America: Morphometric analysis ofAntennaria alborosea,A. corymbosa,A. marginata,A. microphylla,A. parvifolia,A. rosea,andA. umbrinella

Multivariate analysis of vegetative and reproductive characters was used to examine morphological relatedness amongAntennaria alborosea A. E. Porsild,A. corymbosa E. Nels.,A. marginata Greene,A. microphylla Rydb.,A. parvifolia Nutt.,A. rosea Greene, andA. umbrinella Rydb. Both pistillate and staminate plants were examined. Some of the characters examined were variable in one species, but stable in another (i.e., presence or absence of papillae on the achenes). Our analyses indicate that the seven species are morphologically distinct. It is hypothesized that theA. rosea agamic complex arose through hybridization amongA. corymbosa, A. microphylla, A. umbrinella, and possiblyA. dioica (L.)Gaertn. However, hybridization between the three former species and others, as well as their subsequent morphological responses to different environmental conditions causes confusion in recognizing the taxa.Antennaria angustifolia Rydb.,A. arida E. Nels.,A. confinis Greene,A. scariosa E. Nels.,A. foliacea humilis Rydb.,A. concinna E. Nels., andA. viscidula E. Nels. are considered to represent F 1 hybrids.     

Location of amino acid and carbohydrate transport sites in the surface membrane of normal and transformed mammalian cells

Summary Amino acid and carbohydrate transport in normal and malignant transformed hamster cells was studied after binding of the protein Concanavalin A (Con. A) to the surface membrane. Experimental conditions were used so that a similar number of Con. A molecules were bound to both types of cells. The transport of amino acids was inhibited after Con. A binding in the transformed cells but not in normal cells. This was found with the metabolizable amino acidsl-leucine,l-arginine,l-glutamic acid, andl-glutamine, and with the non-metabolizable amino acids cycloleucine and -aminoisobutyric acid. Transport ofd-glucose andd-galactose was more inhibited by Con. A in transformed than in normal cells, and in both types of cellsd-glucose was inhibited more thand-galactose. The inhibition by Con. A on transport was specific, since there was no effect on the transport ofl-fucose in either normal or transformed cells. Con. A also did not effect the entry of 3-0-methyl-d-glucose.These observations can be used to locate amino acid and carbohydrate transport sites in the surface membrane in relation to the binding sites for Con. A. The results indicate that Con. A sites are associated in normal cells with transport sites ford-glucose and to a lesser extentd-galactose, and in transformed cells with transport sites for amino acids and to a greater extent than in normal cells withd-glucose andd-galactose. Malignant transformation of normal cells therefore results in a change in the location of amino acid and carbohydrate transport sites in the surface membrane in relation to the binding sites for Con. A.     

The supraspecific taxonomy and evolution of the fern genusAzolla (Azollaceae)

The systematics of the aquatic fern genusAzolla Lam. is revised at the supraspecific level. Published morphological data are reviewed, and cytological and cladistic analyses of the genus conducted, enabling a discussion of the putative evolutionary trends in the genus, and a revision of the current taxonomy. A phylogenetically more acceptable subgeneric and sectional classification is proposed, viz. subg.Azolla sect.Azolla (comprisingA. filiculoides Lam.,A. rubra R. Br.,A caroliniana auct. nonWilld.,A. microphylla auct. nonKaulf. andA. mexicana Presl), subg.Azolla sect.Rhizosperma (Mey.)Mett. (comprisingA. pinnata R. Br.), and subg.Tetrasporocarpia subg. nov. (comprisingA. nilotica Decne. exMett.).     

Zur taxonomischen Stellung und Nomenklatur vonMicropus longifolius (Compositae-Inuleae)

Zusammenfassung Die unter den NamenMicropus longifolius Boiss. etReut. bzw.Cymbolaena longifolia (Boiss. etReut.)Smoljan. gut bekannte Art wurde zuerst alsStylocline griffithii A.Gray beschrieben. Ihre taxonomische Stellung in bezug auf die GattungenMicropus undStylocline wird diskutiert. Es erscheint am richtigsten, die Art in eine eigene monotypische Gattung zu stellen, ihr korrekter Name ist dannCymbolaena griffithii (A.Gray)Wagenitz, comb. nov.

---

Summary The species usually known asMicropus longifolius Boiss. etReut. orCymbolaena longifolia (Boiss. etReut.)Smoljan. was described for the first time in 1873 asStylocline griffithii A.Gray. The taxonomic position in relation to the generaMicropus andStylocline is discussed. It seems most appropriate to regard this species as belonging to a monotypic genus. In this case its correct name isCymbolaena griffithii (A.Gray)Wagenitz, comb. nov.

     

Studies on aspergilli. VI. The utilization of amino acids in mixtures by some ascosporic members of the aspergillus nidulans group

Summary The utilization of certain amino acids when supplied in three different combinations, (a) glycine, serine, valine, histidine (b) methionine, valine, alanine, arginine (c) leucine, tryptophane, glutamic acid, aspartic acid, byA. nidulans (Eidam)Wint;A. rugulosus Thom andRaper;A. variecolor (Berk. andBr.)Thom andRaper;A. quadrilineatus Thom andRaper andA. violaceus Fennel andRaper was studied through circular partition chromatography. It was found that these Aspergilli which are so closely related morphologically exhibited different rate of assimilation of amino acids. Amino acids in mixtures were utilized better than when supplied singly. Although different species had their own preference to certain amino acids yet there was a simultaneous utilization of both good and poor amino acids.     

Beiträge zur geographischen Pathologie von Suriname

Zusammenfassung Bei einer Reihe von S?ugetieren in Suriname fanden sich in der Milz bei der Untersuchung von Tupfpr?paraten intracellul?r und gelegentlich auch extracellul?r gelagerte Gebilde, die von Histoplasma nicht zu unterscheiden waren. In einer Reihe von F?llen liessen sich die Parasiten auf weisse M?use verimpfen und bei diesen gleichfalls in der Milz zurückfinden. Mitt.:W. A. Collier, A. E. Wolff undA. E. G. Zaal, Documenta Med. Geogr. et Trop.4, 92, 1952; 2. Mitt.:W. A. Collier undW. E. F. Winckel, Z. f. Hyg. [im Druck; 3. Mitt.:C. F. A. Bruyning, Documenta Med. Geogr. et Trop.4, 171, 1952; 4. Mitt.:W. A. Collier undD. A. de la Parra, Documenta Med. Geogr. et Trop. im Druck; 5. Mitt.:W. E. F. Winckel, W. A. Collier undA. E. G. Treurniet, Documenta Med. Geogr. et Trop. im Druck.     

Seasonal and annual variations in biological regime of lakes in an ultracontinental climate (Trans-Baikal Region of U.S.S.R)

Summary The lakes are covered 7 months with ice, but under the transparent ice (up to 180 cm thickness) a rich vegetation of phytoplankton, phytomicrobenthos and macrophyta develop and activate the bacterial and animal population. Winter production of the phytoplankton reaches 36 g/m² C and that of the phytomicrobenthos 70 g/m² C.The water levels of the lakes show fluctuations with an amplitude of 2–4 m, affecting the whole trophic system inclusive species composition, proportion and abundance of individual aquatic organisms as well as related abiotic conditions.Co-authors: E. I. Bondereva, T. N. Morozova, (primary production), A. A. Topolov, K. A. Shishkina (microbiology), V. P. Gorlachov (zooplankton), I. M. Shapovalova (zoobenthos), N. M. Pronin (fish and their parasites), V. N. Kuzmich (nutrition of fish).Co-authors: E. I. Bondereva, T. N. Morozova, (primary production), A. A. Topolov, K. A. Shishkina (microbiology), V. P. Gorlachov (zooplankton), I. M. Shapovalova (zoobenthos), N. M. Pronin (fish and their parasites), V. N. Kuzmich (nutrition of fish).     

The species ofAphelinus Dalman, 1820 [Hymenoptera: Aphelinidae] from India

An account of the Indian species of the genusAphelinus Dalman is given Two new species (A. kashmiriensis sp. n.,A. desantisi sp.n.) are described. Four species (A. nikolskajae Jasnosh,A. flavipes (Foerster),A. abdominalis (Dalman),A. asychis Walker) are reported for the first time from India. A key for the separation of the Indian species ofAphelinus is presented.

---

Résumé Deux nouvelles espèces (A. kashmiriensis, A. desantisi) sont décrites. Quatre espèces (A. nikolskajae Janosh,A. flavipes (Foerster),A. abdominalis (Dalman),A. asychis Walker) sont signalées pour la première fois de l’Inde. Une clé de détermination des espèces indiennes deAphelinus est présentée.

     

Fungi that cause mouldiness of processed sheet rubber in Western Nigeria

The fung isolated from mouldy processed sheet rubber in Western Nigeria wereAspergillus fumigatus Fres,Aspergillus flavus Link andAspergillus aculeatus Iisuka. When inoculated on sterilized, uninfected sheet rubber, bothA. fumigatus andA. flavus produced symptoms which were similar to those originally observed on mouldy processed sheet from the rubber estate.

---

Zusammenfassung Die folgenden Pilze sind vom verschimmelten, bearbeiteten Rubber isoliert worden:Aspergillus fumigatus Fres,A. flavus Link andA. aculeatus Iisuka. WennA. fumigatus undA. flavus an sterilisiertem, nicht infiziertem Rubber verimpft worden sind, haben sie identische Läsionen am sterilen Rubber verursacht.

     

Racemic Resolution of some <Emphasis Type="SmallCaps">dl</Emphasis>-Amino Acids using <Emphasis Type="Italic">Aspergillus fumigatus</Emphasis><Emphasis Type="SmallCaps">l</Emphasis>-Amino Acid Oxidase

The ability of Aspergillus fumigatus l-amino acid oxidase (l-aao) to cause the resolution of racemic mixtures of dl-amino acids was investigated with dl-alanine, dl-phenylalanine, dl-tyrosine, and dl-aspartic acid. A chiral column, Crownpak CR+ was used for the analysis of the amino acids. The enzyme was able to cause the resolution of the three dl-amino acids resulting in the production of optically pure d-alanine (100% resolution), d-phenylalanine (80.2%), and d-tyrosine (84.1%), respectively. The optically pure d-amino acids have many uses and thus can be exploited industrially. This is the first report of the use of A. fumigatus l-amino acid oxidase for racemic resolution of dl-amino acids.     

The alternative<Emphasis Type="SmallCaps"> d</Emphasis>-galactose degrading pathway of<Emphasis Type="Italic"> Aspergillus nidulans</Emphasis> proceeds via<Emphasis Type="SmallCaps"> l</Emphasis>-sorbose

The catabolism of d-galactose in yeast depends on the enzymes of the Leloir pathway. In contrast, Aspergillus nidulans mutants in galactokinase (galE) can still grow on d-galactose in the presence of ammonium—but not nitrate—ions as nitrogen source. A. nidulans galE mutants transiently accumulate high (400 mM) intracellular concentrations of galactitol, indicating that the alternative d-galactose degrading pathway may proceed via this intermediate. The enzyme degrading galactitol was identified as l-arabitol dehydrogenase, because an A. nidulans loss-of-function mutant in this enzyme (araA1) did not show NAD⁺-dependent galactitol dehydrogenase activity, still accumulated galactitol but was unable to catabolize it thereafter, and a double galE/araA1 mutant was unable to grow on d-galactose or galactitol. The product of galactitol oxidation was identified as l-sorbose, which is a substrate for hexokinase, as evidenced by a loss of l-sorbose phosphorylating activity in an A. nidulans hexokinase (frA1) mutant. l-Sorbose catabolism involves a hexokinase step, indicated by the inability of the frA1 mutant to grow on galactitol or l-sorbose, and by the fact that a galE/frA1 double mutant of A. nidulans was unable to grow on d-galactose. The results therefore provide evidence for an alternative pathway of d-galactose catabolism in A. nidulans that involves reduction of the d-galactose to galactitol and NAD⁺-dependent oxidation of galactitol by l-arabitol dehydrogenase to l-sorbose.     

Morphological and cytological evidence for polyphyletic allopolyploidy inArctostaphylos mewukka (Ericaceae)

The central Sierran tetraploidArctostaphylos mewukka Merriam has been reported to be an allopolyploid originating from the diploid species,A. patula Greene and eitherA. viscida subsp.viscida Parry orA. viscida subsp.mariposa (Dudley)P. V. Wells, although without conclusive evidence. Morphometrics and the verification and determination of chromosome numbers were used to substantiate the evolutionary relationships among these species. A closely related species,Arctostaphylos truei Knight, was also examined using these methods to determine its separability fromA. mewukka. The morphometric analyses support a hypothesis for a polyphyletic origin ofA. mewukka from different races ofA. viscida andA. patula. The chromosomal data, although inclusive, also support this hypothesis. The data do not support the recognition ofA. truei as a taxonomic entity separate fromA. mewukka at the species level.     

Novos Deuteromycetes da micogeografia intercontinental

Summary This paper deals with some interesting new fungi which are described as a contribution for the development of the Mycogeography.Arbuscula Batista &Peres n. gen. is studied as a member of the family Stilbaceae havingA. eugeniae Batista &Peres n. sp. on leaves ofEugenia jambolana Lam. from Lucknow, India, as the type species. Another new genus isEllisia Batista &Peres, typified byE. ingae Batista &Peres n. sp. on leaves ofInga fagifolia (L.)Willd. from Manaus. Amazonas, Brazil. Two new binomia are:Eriomycopsis paraensis Batista &Peres n. sp. on leaves ofBertholletia excelsa H.B.K. from Belem, State of Pará, Brazil,Sporidesmium americanense Batista &Peres n. sp. on leaves ofQuercus wislizenii A.D.C., from U.S.A. andSporidesmium cookei (Hughes)W. B. Ellis, on leaves of Lauraceae, from Manaus.

---

Zusammenfassung Diese Arbeit bringt einige interessante neue Pilze, welche als Beitrag zur Entwicklung der Mycogeographie beschrieben werden.Arbuscula Batista &Peres n. gen. wurde studiert als ein Mitglied der Familie Stilbaceae, dessen TypusA. eugeniae Batista &Peres n. sp. sich auf Blättern vonEugenia jambolana Lam. aus Lucknow, Indien, befand. Eine andere neue Gattung istEllisia Batista &Peres, typiziert durchE. ingae Batista &Peres n. sp. auf Blättern vonInga fagifolia (L.)Willd. aus Manaus, Amazonas, Brasilien. Zwei neue Binome sind:Eriomycopsis paraensis Batista &Peres n. sp. auf Blättern vonBertholletia excelsa H.B.K. aus Belém, Staat Pará, Brasilien,Sporidesmium americanense Batista &Peres n. sp. auf Blättern vonQuercus wislizenii A.D.C. aus U.S.A. undSporidesmium cookei (Hughes)W. B. Ellis, auf Blättern von Lauraceae, aus Manaus, Amazonas.

---

---

Dedicado à Mrmória do Prof.Raffaele Ciferri     

Die einjährigen Arten der GattungArnebia Forsk.

Zusammenfassung Die einjährigen Arten der GattungenArnebia werden, teilsJohnston, teilsPopov folgend, in die zwei UntergattungenArnebia undStrobila, letztere die SektionenStrobila undCornutae umfassend, gegliedert und die insgesamt 16 Arten, von denenA. johnstonii H.Riedl,A. waziristanica H.Riedl undA. simulatrix H.Riedl neu sind, ihrer Morphologie und systematischen Stellung nach besprochen.Durchgeführt mit Unterstützung durch National Science Foundation Grant G 16325.Die Zeichnungen wurden von FrauErika Kubelka ausgeführt, wofür ihr auch an dieser Stelle aufrichtigster Dank gesagt sei.     

Identification and characterization of the bacterial <Emphasis Type="SmallCaps">d</Emphasis>-gluconate dehydratase in <Emphasis Type="Italic">Achromobacter xylosoxidans</Emphasis>

Achromobacter xylosoxidans is known to utilize d-glucose via the modified Entner-Doudoroff pathway. Although d-gluconate dehydratase produced from this bacterium was purified and partially characterized previously, a gene that encodes this enzyme has not yet been identified. To obtain protein information on bacterial d-gluconate dehydratase, we partially purified d-gluconate dehydratase in A. xylosoxidans and investigated its biochemical properties. Two degenerate primers were designed based on the N-terminal amino acid sequence of the partially purified d-gluconate dehydratase. Through PCR performed using degenerate primers, a 1,782-bp DNA sequence encoding the A. xylosoxidans d-gluconate dehydratase (gnaD) was obtained. The deduced amino acid sequence of A. xylosoxidans gnaD showed strong similarity with that of proteins belonging to the dihydroxy-acid dehydratase/phosphogluconate dehydratase family (COG0129). This is in contrast to the archaeal d-gluconate dehydratase, which belongs to the enolase superfamily (COG4948). The phylogenetic tree showed that A. xylosoxidans d-gluconate dehydratase is closer to the 6-phosphogluconate dehydratase than the dihydroxy-acid dehydratase. Interestingly, a clade containing A. xylosoxidans enzyme was clustered with proteins annotated as a second and a third dihydroxy-acid dehydratase in the genomes of Clostridium acetobutylicum (Cac_ilvD2) and Streptomyces ceolicolor (Sco_ilvD2, Sco_ilvD3), indicating that the function of these enzymes is the dehydration of d-gluconate.     

Immunohistochemistry of endogenous l-DOPA in the rat posterior hypothalamus

Summary The aim of this work was to study l-DOPA-containing neuronal structures of the rat posterior and dorsal hypothalamus by means of immunohistochemistry using antiserum against glutaraldehyde conjugated l-DOPA. Aspects and distribution of l-DOPA immunoreaction among cells of the supramammillary nucleus and the A11, A13c and A13 cell groups are described and compared to dopamine immunoreactivity, mainly through a double colored labelling procedure employing a color modification of the DAB reaction by metallic ions. Differences between l-DOPA and dopamine stainings within cell groups as the presence of cells with predominant or exclusive l-DOPA coloration are tentatively explained under the light of previous findings using immunohistochemistry of catecholamines synthesizing enzymes and catecholamines histofluorescence.     

La pyrimidine (2-méthyl-4-amino-5-amino-méthylpyrimidine), facteur de croissance de microorganismes (Rhodotorula,Mucorinées,Dematium)

Sans résuméNous exprimons toute notre reconnaissance à la Direction des Etablissements Dr. A.Wander A. G. (Berne), pour son appui; nous sommes redevables au Dr. R. J.Williams (Corwallis, Oregon) d'un échantillon d'acide pantothénique, aux EtablissementsHoffmann. La Roche Bâle (Département scientifique, Dr. M.Guggenheim) des diverses pyrimidines utilisées, et au Prof.Hörlein, I. G. Farbenindustrie A. G. de l'aneurine synthétique employée. Nous les remercions très vivement.     

Influence of 2,4-D,TIBA and 3,5-D on the growth response of cultured maize embryos

Induction of embryogenic calli from immature zygotic embryos of maize requires the presence of 2,4-D or similar auxin-like growth regulators in the culture medium. Pulse-chase experiments with 2,4-D, using various concentrations of 2,4-D in the induction medium were tested in relation to induction of callus in the embryogenic inbred line A188 and the non-embryogenic inbred A632. Interactions of 2,4-D, 3,5-D and the auxin transport inhibitor TIBA were also studied. Pulse-chase experiments showed that exposure to 2,4-D influenced the culture response from 0.5 h onwards. After a pulse of 0.5 h, shoot and root elongation of the embryo was stimulated. A pulse of 16 h or longer induced outgrowths and callus formation at the basal side of the scutellum. Pulses of 7 days and longer resulted in the induction of friable embryogenic Type II callus in A188. Embryos were cultured at 2,4-D concentrations ranging from 0.002 to 2000 mg l⁻¹ and optimal concentration for the induction of embryogenic callus in A188 was 2 mg l⁻¹. At lower concentrations there was a transition between callus formation and germination; at increasing concentrations, callus induction was reduced and finally growth responses became blocked. When TIBA was added to medium without 2,4-D, root elongation decreased in a dose-dependent way suggesting the need of polar transport of endogenous auxins for root elongation. When added to medium with 2,4-D, TIBA caused suppression of callus formation, again pointing to the necessity of polar transport of 2,4-D. In combination with 2,4-D, cultures with 3,5-D resembled cultures at lower 2,4-D concentrations, pointing to a competitive interaction between 3,5-D and 2,4-D. This revised version was published online in June 2006 with corrections to the Cover Date.     

Regulation of biosynthesis of monensins on chemically defined medium

Addition ofL-valine andDL-isoleucine to the cultivation medium ofStreptomyces cinnamonensis was found to affect the ratio of synthesized monensins A and B. In the presence ofL-valine monensin A is synthesized predominantly, whereas in the presence ofDL-isoleucine the production of monensin B increases.