Microbial mineralization of organic phosphate in soil

Summary Phosphate-dissolving microorganisms were isolated from non-rhizosphere and rhizosphere of plants. These isolates included bacteria, fungi and actinomycetes. In broth cultures, Gram-negative short rod,Bacillus andStreptomyces species were found to be more active in solubilizing phosphate thanAspergillus, Penicillium, Proteus, Serratia, Pseudomonas andMicrococcus spp. The sterile soils mixed with isolated pure culture showed slower mineralization of organic phosphate than that of non-sterile soil samples at all incubation periods. Maximum amount of phosphate mineralization by isolated microorganisms were obtained at the 60th and the 75th day of incubation in sterile and non-sterile soils respectively. The mixed cultures were most effective in mineralizing organic phosphate and individuallyBacillus sp. could be ranked next to mixed cultures. Species ofPseudomonas andMicrococcus were almost the same as that of the control under both sterile and non-sterile conditions.     

Geochemical aspects of aluminium in forest soils in Galicia (N.W. Spain)

The aqueous speciation of Al was studied in acid forest soils in N.W. Spain. Aluminum concentrations were 10–70 mol L^–1, with variable proportions oflabile, nonlabile, andacid-soluble Al. Almost all thelabile Al was found complexed with F^–, Al³⁺ concentrations being low. The importance of organic matter was seen in the formation of Al-organic complexes in the solid soil fraction and the presence of aqueous alumino-organic complexes in superficial horizons (umbric epipedons) rich in organic matter.     

Microfungal species composition and fungal biomass in a coniferous forest soil polluted by alkaline deposition

Isolations of soil microfungi from the humus (F/H-layer) of a coniferous forest soil which was either unpolluted (pH 4.1) or polluted (pH 6.6) for 25 years by deposition of alkaline dust, were made by soil washing and spore plating. Both techniques revealed similar changes in species composition. Alkaline dust exposure caused a reduction in overall species numbers, but led to higher relative isolation frequencies of Mortierella alpina, Oidiodendron tenuissimum, Penicillium montanese, Sagenomella verticillata, and Trichosporiella sporotrichioides. The incidence of M. isabellina, O. cf. clamydosporium, P. spinulosum, Penicillium sp. 1, P. sclerotiorum, Trichoderma viride, and Verticillium bulbillosum was reduced on polluted sites. The amount of the mainly fungal-derived phospholipid fatty acid 18 : 26 decreased by 23%, while the amount of ergosterol increased by 9% in the polluted soil. Offprint requests to: H. Fritze.     

Plant growth regulatory metabolites from novel actinomycetes

Metabolites from 796 isolates of aerobic actinomycetes were screened for plant growth regulatory properties using an algal bioassay. These included 266 isolates ofStreptomyces, 28 unidentified actinomycetes, and 502 isolates of novel actinomycetes represented by 18 genera. Algal growth inhibition of 30% was observed with 60 isolates, 37 of which belonged to the genusStreptomyces. Among other inhibitors were 8 isolates ofActinomadura, 6 ofActinoplanes, 2 each of the generaThermomonospora, Streptoverticillium, andPromicromonospora, and 3 unidentified. Metabolites from 70 isolates promoted algal growth by 20%. These included 13 isolates ofMicromonospora, 11 ofStreptomyces, 6 ofNocardia, 5 ofActinomadura, and 4 each ofRhodococcus andThermomonospora. Sixteen unidentified isolates; 3 isolates ofPromicromonospora; 2 isolates each ofActinoplanes, Streptosporangium, andOerskovia; and 1 of Thermoactinomyces peptonophilus-like organism andSaccharomonospora viridis also promoted the algal growth by 20%. The plant growth inhibitory properties of 9 actinomycetes and the growth promoting properties of 6 were demonstrable during the secondary screening on higher plants using chemicals extracted from the culture broth. The metabolites fromMicromonospora, Nocardia, Rhodococcus, Streptosporangium, andOerskovia isolates were associated with plant growth promotion only; those fromStreptomyces were most frequently involved with the growth inhibition.This is Michigan Agriculture Experiment Station Journal Article No. 12191.     

Genotype-environment interaction for awn development in isogenic lines of barley

Summary Awn length of four isogenic lines of barley differing by two genes for awn development (A andB) and their short iinkage blocks was evaluated at a wide range of plant densities (0.002 to 3.345 m²/plant) for two years. Awn development was reduced at high plant density. The quarter-awned genotype (aaBB) became phenotypically awnless (aabb) at high plant density. Similar results were obtained each year and the genotype x plant density effect was the major portion of the genotype-environment interaction variance. Additive ( _A , _B ) and additive x additive ( _AB ) gene effects were computed for each plant density for lateral and central floret awn length. For lateral awns _AB was not affected, but _A and _B increased with decreased plant density. In contrast, for central awns _A and _AB decreased and _B increased with decreased plant density.Central floret awns measured at each spike node showed that high plant density reduced awn development most in the lower half of the spike. This is the zone of most rapid awn differentiation and since culm elongation and spike growth rates were greatly increased by high plant density, it was suggested that rapid growth invoked a stress on awn development and differentially altered the expression ofA andB.

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Zusammenfassung An 4 isogenen Gerstenlinien, die sich durch zwei Gene für Grannenbildung (A undB) und entsprechende kurze Kopplungsblocks unterscheiden, wurde zwei Jahre lang die Länge der Grannen bei verschiedener Standdichte (0,002 bis 3,345 m² je Pflanze) untersucht. Bei dichtem Bestand ergab sich eine Beeinträchtigung der Grannenbildung, der viertelbegrannte Genotyp (aaBB) wurde phänotypisch grannenlos (aabb). Die Ergebnisse stimmten in beiden Jahren überein, der Effekt Genotyp x Standdichte hatte den Hauptanteil an der Interaktionsvarianz Genotyp: Umwelt. Additive ( _A , _B ) und additive x additive ( _AB ) Genwirkungen wurden bei jeder Standdichte für die Grannenlänge der Seiten-und Mittelährchen errechnet. Bei den seitlichen Grannen wurde _AB nicht beeinflußt, aber _A und _B erhöhten sich mit abnehmender Standdichte. Im Gegensatz dazu gingen bei den mittleren Grannen _A und _AB zurück, während für _B bei abnehmender Standdichte ein Ansteigen festzustellen war.Messungen der mittleren Grannen jeder Ähre zeigten, daß hohe standdichte der Pflanzen die Grannenbildung am meisten in der unteren Hälfte der Ähre reduzierte. Das ist die Zone, in der sich die Grannen am schnellsten differenzieren, und da die Halm- und Ährenwachstumsraten durch hohe Standdichte stark gesteigert wurden, scheint das schnelle Wachstum auf die Grannenentwicklung hemmend einzuwirken und die Manifestierung vonA undB unterschiedlich abzuändern.

     

Distributional patterns of mesophilous and thermophilous microfungi in two bahamian soils

This study focuses on the characteristics displayed by mesophilous and thermophilous microfungal populations occurring in two tropical monodominant plant communities, a Cocos nucifera grove and a Casuarina equisetifolia forest, that provide distinctly different edaphic conditions. The mesophilous population sampled at 25°C by the dilution plate method and the thermophilous population that developed on soil plates incubated at 45°C consisted of 1693 isolates representing 60 species and 29 genera and 8887 isolates representing 20 species and 10 genera, respectively. The mesophilous propagules averaged 9,990 per gram dry soil in the coconut grove that lacks a litter layer, is low in moisture and organic matter and is subjected to high solar irradiation. The population was characterized by the prevalence of aspergilli and dematiaceous-sphaeropsidaceous forms and the near absence of mucoraceous isolates. Ascomycetes were common. The only widespread taxa were the three species, Aspergillus niger, Penicillium chrysogenum, and Cladosporium cladosporioides. Species diversity was high and 73% of the isolates were cellulolytic. In the casuarina forest, adequate moisture and organic matter and a protecting litter layer provide a mesic environment. The mean number of mesophilous fungi per gram dry soil was 32,800. This figure is considerably lower than ones reported for mesic temperate communities and may be due to more rapid propagule removal through accelerated microfaunal and microbial activity. An abundance of mucoraceous and moniliaceous isolates and penicillia, and the rarity of aspergilli, dematiaceous-sphaeropsidaceous forms and ascomycetes characterize the population. The infrequency of aspergilli is thought to be due to their poor competitive ability. Eight species, Absidia cylindrospora, Penicillium notatum, Pestalotia cocculi?, Cylindrocarpon heteronema, Gliocladium roseum, Trichoderma viride, Paecilomyces marquandii, and Penicillium funiculosum were widespread in the area. Species diversity equaled that observed in mesic temperate communities. Less than one third of the isolates were cellulolytic. Phytopathogens were common, a feature characteristic of tropical populations. Thermophilous fungi averaged 33 per gram dry soil in the casuarina forest and increased to 943 per gram in the insolated soil of the coconut grove. Thermotolerant forms (94% of the isolates) were abundant and were principally species of Aspergillus and Chaetomium. Thermophilic fungi were rare and of the six species isolated only Chaetomiun britannicum was widespread. Four species, Ch. osmaniae, Ch. medusarum, Ch. sulphureum, and Thielavia arenaria, appear to be new records for western hemisphere soils.     

Fruiting studies in species ofCapronia (Herpotrichiellaceae)

A recently described protocol for thein vitro production of ascomata was employed to determine the sexual incompatibility systems of five species ofCapronia. The formation of mature ascomata in isolates derived from single ascospores demonstrated thatC. epimyces, C. mansonii, andC. munkii n. sp. are homothallic. In contrast, fertile ascomata were observed only in mass-ascospore isolates and pairwise crosses between specific single-ascospore isolates inC. dactylotricha n. sp. andC. moravica. TheExophiala anamorphs ofC. dactylotricha andC. munkii are described and aPhialophora-like synanamorph is reported for the former species. Germinating ascospores ofC. munkii formed conidiogenous cells directly, while the ascospores of the remaining species germinated to produce germ tubes and hyphae. The application of the terms microcyclic conidiation to secondary conidium production and sclerotial body and stroma to the multicellular structures produced by species ofCapronia andExophiala are discussed.     

Interactions between freshwater bacteria andAnkistrodesmus braunii in batch and continuous culture

Batch and continuous cultures ofAnkistrodesmus braunii were established in an inorganic medium with growth rate limited by P. In batch culture, inoculation of lake water bacterial isolates ofPseudomonas sp. andFlavobacterium sp. showed that thePseudomonas isolate was capable of more rapid growth on algal exudates of lytic products than was theFlavobacterium isolate. When inoculated singly into a continuous culture (D=0.267 day^–1; P level, 2M), theFlavobacterium isolate initially caused a decrease in the population density of the alga, but then steady states for both organisms were obtained. ThePseudomonas isolate under the same conditions caused a rapid washout of the algal culture, and steady-state conditions were never obtained. When thePseudomonas isolate was added to the two-member, steady-state system ofA. braunii andFlavobacterium, the algal population again washed out of the vessel, followed by theFlavobacterium and then thePseudomonas isolate. A transient increase in the P concentration to 200M in the culture vessel caused the low algal population level to increase, followed by increases in the bacterial isolates when the algal population was high enough to supply the required organic carbon source. The system demonstrated that competition for P between the alga and the bacteria can occur, and the results were dependent on the algal and bacterial relative growth rates. The bacterial growth rates were limited initially by organic substrates produced by the alga, and the different bacterial isolates competed for these substrates.     

Plant- and soil related controls of the flow of carbon from roots through the soil microbial biomass

The flow of carbon from plant roots through the microbial biomass is one of the key processes in terrestrial ecosystems. Roots release considerable amounts of organic materials which are utilized by microbes as substrate for biosynthesis and energy supply. The fate of photosynthates and other organic material in the soil-root environment under different conditions was studied using¹⁴C-tracers. Soil structure and texture had a large effect on the turnover of the¹⁴C-labelled materials through the microbial biomas. Finer, clayey soils tended to be more preservative than coarser, sandy soils,i.e., larger amounts of¹⁴C were incorporated in microbial biomass and soil organic matter fractions in clayey soils than in sandy soils.The soil nutrient status also appeared to affect organic matter turnover. At limiting plant-nutrient concentrations the utilization of¹⁴C-labelled photosynthates seem to be hampered. Plant roots influenced the transformation of glucose and crop residues and the effect was attributed to plant-induced changes in mineral nutrient status. The mechanisms of this process and the consequences are discussed.A number of areas for future research are identified, including the potentials for manipulating rhizodeposition.     

Studies on microbial antagonism in the establishment of clover pasture

Summary Fungi inhabiting soil recently cleared of the native vegetation have been isolated and compared with those isolated from under established clover pastures, Three methods of isolation of the fungi were used in each situation, and profoundly influenced the population obtained.In newly cleared soils the composite fungal population pattern deduced all three isolation methods comprised species of Mortierella, Phoma, Trichoderma, Penicillium, Fusarium, Sclerotium and non-sporing mycelia. In soil supporting established clover pastures the main rhizosphere fungi were species of Fusarium, Aspergillus, Phoma, Curvularia, Macrophomina, Sclerotium and one Ascomycete.Fusarium oxysporum was the most frequently isolated fungus.Conventional plating techniques suggested that the dominant fungi in the rhizosphere of clover wereFusarium oxysporum andAspergillus versicolor, whereas isolation of fungi from hyphae adhering to the clover roots indicated that species of Macrophomina, Curvularia and an Ascomycete were the most abundantly occurring organisms. In the case of the root residues of the native vegetation in newly cleared soils plating techniques resulted in species of the freely sporing Mortierella, Trichoderma, Aspergillus, Fusarium and Penicillium occurring most frequently, whereas the isolation of fungi from hyphal strands on the residues gave a population pattern dominated by species of Mortierella, Phoma, Sclerotium, and non-sporing mycelia.The study indicated a marked succession of fungal species during the decomposition of the root debris in newly cleared soils, and also that some early members of this changing population might exert an adverse effect on the establishment of clover.     

A simple and rapid technique for fluorescence staining of fungal nuclei

A technique for staining fungal nuclei using fluorescence stain Hoechst Dye 33258 in McIlvaine standard buffer of pH 7.26–7.44 is reported. It is a broad-spectrum fungal nuclear staining tool found to be effective onAgaricus bisporus, Alternaria helianthi, Fusarium oxysporum f. sp.lini, Penicillium binellum, Pythium ultimum, Rhizoctonia solani, andSaccharomyces cerevisiae. Conidial nuclei ofAlternaria helianthi, Fusarium oxysporum f. sp.lini, andPenicillium binellum also stained well.     

New <Emphasis Type="Italic">Penicillium</Emphasis> and <Emphasis Type="Italic">Talaromyces</Emphasis> species from honey,pollen and nests of stingless bees

Penicillium and Talaromyces species have a worldwide distribution and are isolated from various materials and hosts, including insects and their substrates. The aim of this study was to characterize the Penicillium and Talaromyces species obtained during a survey of honey, pollen and the inside of nests of Melipona scutellaris. A total of 100 isolates were obtained during the survey and 82% of those strains belonged to Penicillium and 18% to Talaromyces. Identification of these isolates was performed based on phenotypic characters and β-tubulin and ITS sequencing. Twenty-one species were identified in Penicillium and six in Talaromyces, including seven new species. These new species were studied in detail using a polyphasic approach combining phenotypic, molecular and extrolite data. The four new Penicillium species belong to sections Sclerotiora (Penicillium fernandesiae sp. nov., Penicillium mellis sp. nov., Penicillium meliponae sp. nov.) and Gracilenta (Penicillium apimei sp. nov.) and the three new Talaromyces species to sections Helici (Talaromyces pigmentosus sp. nov.), Talaromyces (Talaromyces mycothecae sp. nov.) and Trachyspermi (Talaromyces brasiliensis sp. nov.). The invalidly described species Penicillium echinulonalgiovense sp. nov. was also isolated during the survey and this species is validated here.     

Decomposition of organic matter by fungi in saline soils

The object of the present investigation was to study the fungal decomposition of organic matter from different sources, added to the saline soils. The organic matter added was in the form of fresh cuttings of two salt tolerant harbaceous plants namelyDiplachne fusca (Kallar grass) andSesbania aculeata (Dhancha). In addition to these treatments, farm yard manure and press mud (waste of sugar industry) were also used as a source of organic matter. Twelve combinations of these treatments were studied. A number of fungi were isolated from differently treated saline soils incubated at 30 °C. Among the fungi isolatedAspergillus spp. andFusarium solani had the highest frequency of occurrence. The relative cellulolytic ability of 10 fungal species was also estimated.Alternaria humicola andNigrospora sp. were found to be the most cellulolytic among the fungi isolated. The decrease in organic matter due to microbial decomposition was found to be most rapid during first two weeks of incubation. Among the treatments with one organic matter source, press mud produced maximum humus equal to 0.28 %. The pH and electrical conductivity increased slightly due to the closed system where no leaching took place.     

Isolation of endophytic fungi from tropical forest in Indonesia

Endophytic fungi (EPF) are an important contributor to fungal diversity. It is surmised that EPF colonizing plant roots have high diversity. This study aimed to alleviate the scarcity of information regarding EPF in tropical forests, by isolationg and identifying EPF from a tropical forests in Indonesia. Soils were collected from five forests: (1) Tectona grandis monoculture; (2) Swietenia macrophylla monoculture; (3) Gmelina sp., Artocarpus champeden, Dipterocarp mixed; (4) Dipterocarp primary; (5) Macaranga sp. secondary. Four trees (Calliandra calothyrsus, Paraserianthes falcataria, Sesbania grandiflora, and Cassia siamea) and three crops (Sorghum bicolor, Allium fistulosum, and Trifolium repens) were grown in the forest soils to trap EPF. EPF were isolated from roots and isolation rates were calculated. Based on the isolation rates, P. falcataria and S. bicolor were chosen and grown again in forest soils. EPF were isolated and identified by their rDNA ITS1 region. Twelve and 21 EPF were isolated from 250 roots of P. falcataria and 300 roots of S. bicolor, respectively. Identified EPF were from genera Acrocalymma, Fusarium, Tolypocladium, Penicillium, Talaromyces, Exophiala, Dictyosporium, Pseudochaetosphaeronema, Mariannaea, Trichoderma, and Mycoleptodiscus. Acrocalymma, Tolypocladium, Penicillium, Exophiala, Pseudochaetosphaeronema, Mariannaea, and Mycoleptodiscus spp. were isolated from only one forest. Fusarium, Talaromyces, and Trichoderma spp. were isolated from more than one forest. The numbers of EPF isolated from Gmelina sp., Artocarpus champeden, Dipterocarp mixed forest, and Macaranga sp. secondary forest were higher than those from other forests, suggesting that different plant species in forests affect the root EPF community.     

Visualization of the cytoskeleton in Leydig cells in vitro

Summary Effect of LH, vinblastine and cytochalasin B on the cytoskeleton of cultured Leydig cells was investigated using monoclonal antibodies and fluorescence microscopy. After LH addition and treatment with cytoskeletal disrupting drugs, three main effects were observed: 1) increase of androgen level secreted by cultured mouse Leydig cells, 2) changes of cell-shape towards regular and rounded, 3) increase of ⁵,3-HSD activity. The results are discussed in respect to possible involvement of cytoskeleton in the regulation of steroidogenesis.     

Ein Verfahren zur näherungsweisen Berechnung des Fruchtvolumens bei Äpfeln

Zusammenfassung Unter Berücksichtigung des Fruchtformindexes h/Ø der einzelnen Frucht kann man den Volumzuwachs beliebig zusammengesetzter Gruppen von Früchten an verschiedenen Bäumen vergleichen. Bei der Berechnung der Zuwachsraten des Fruchtvolumens braucht man nur Durchmesser und Höhe der Früchte zu kennen, um das tatsächliche Volumen in guter Annäherung zu berechnen. Die Daten der Regression des Korrekturfaktors für das Volumen (K ) auf den Fruchtformindex werden für vier Sorten stark unterschiedlicher Fruchtform angegeben. Das Volumen der Frucht wird nach folgender Formel berechnet: V = 4/3 · · r ³ · K . Vergleichende Untersuchungen über die Zuwachsrate verschiedener Sorten können bei Verwendung der sortentypischen Regressionen durchgeführt werden.

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A method for approximate calculation of fruit volume in apples

Summary Growth rates of fruit volume can be determined more precisely by using the index h/Ø (length of fruit/diameter) than by simply calculating the volume of a sphere based on the measured diameter. Fruit volume is to be calculated by: V = 4/3 · · r ³ · K K is the factor of deviation of fruit shape from a sphere. K is given for 4 different varieties with varying shape of fruits (Echter Winterglockenapfel, Golden Delicious, Cox Orange Pippin and Ingrid Marie). The increase in volume of any group of apples within one variety or of different varieties can be compared by means of the specific regression of h/Ø to K .

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Obstbauversuchsanstalt des Alten Landes in Jork     

Plant community influences on soil microfungal assemblages in boreal mixed-wood forests

We studied the relationships between assemblages of soil microfungi and plant communities in the southern boreal mixed-wood forests of Quebec. Sampling took place in 18,100 m2 plots from an existing research site. Plots were separated into three categories based on dominant overstory tree species: (i) trembling aspen, (ii) white birch and (iii) a mixture of white spruce and balsam fir. Within each plot a 1 m2 subplot was established in which the understory herbaceous layer was surveyed and soil cores were collected. Microfungi were isolated from soil cores with the soil-washing technique and isolates were identified morphologically. To support our morphological identifications DNA sequences were obtained for the most abundant microfungi. The most frequently occurring microfungal species were Penicillium thomii, P. spinulosum, P. janthinellum, Penicillium sp., P. melinii, Trichoderma polysporum, T. viride, T. hamatum, Mortierella ramanniana, Geomyces pannorum, Cylindrocarpon didymum, Mortierella sp. and Mucor hiemalis. Multivariate analyses (redundancy analysis followed by variance partitioning) revealed that most of the variation in microfungal communities was explained by understory plant species composition as opposed to soil chemistry or overstory tree species. In this floristically diverse system saprophytic microfungal assemblages were not correlated with the overstory tree species but were significantly correlated with the main understory herbs, thereby reflecting differences at a smaller spatial scale.     

Actinomycetes isolated from medicinal plant rhizosphere soils: diversity and screening of antifungal compounds,indole-3-acetic acid and siderophore production

A total of 445 actinomycete isolates were obtained from 16 medicinal plant rhizosphere soils. Morphological and chemotaxonomic studies indicated that 89% of the isolates belonged to the genus Streptomyces, 11% were non-Streptomycetes: Actinomadura sp., Microbispora sp., Micromonospora sp., Nocardia sp, Nonomurea sp. and three isolates were unclassified. The highest number and diversity of actinomycetes were isolated from Curcuma mangga rhizosphere soil. Twenty-three Streptomyces isolates showed activity against at least one of the five phytopathogenic fungi: Alternaria brassicicola, Collectotrichum gloeosporioides, Fusarium oxysporum, Penicillium digitatum and Sclerotium rolfsii. Thirty-six actinomycete isolates showed abilities to produce indole-3-acetic acid (IAA) and 75 isolates produced siderophores on chrome azurol S (CAS) agar. Streptomyces CMU-PA101 and Streptomyces CMU-SK126 had high ability to produced antifungal compounds, IAA and siderophores.     

Forskolin increases osmotic water permeability of rabbit cortical collecting tubule

Summary Forskolin is a unique diterpene that may directly activate the catalytic subunit of adenylate cyclase. We therefore examined the effect of 50 m forskohn on osmotic water permeability in rabbit cortical collecting tubules perfusedin vitro. Forskolin increased net volume flux (J _v , from 0.30 to 1.22 nl/mm/min,P<0.02) in all tubules. The hydro-osmotic effect of forskolin was similar with respect to magnitude and time course to that produced by a maximal dose (250 U/ml) of arginine vasopressin. An additive effect onJ _v andL _p was not observed when maximal concentrations of forskolin and arginine vasopressin were given simultaneously. The compound d(CH₂)₅Tyr(Et) VAVP, which noncompetitively inhibits the vasopressin receptor, significantly reduced collecting tubular hydro-osmotic response to arginine vasopressin. In contrast, the hydro-osmotic response to forskolin was maintained in the presence of d(CH₂)₅ Tyr(Et)VAVP. However, the hydro-osmotic response to forskolin could be inhibited by 1.0 m guanine 5-(,-imido) triphosphate (GppNHp) and by the calmodulin inhibitor N-(6-amenohexyl)-5-chloro-1-naphthalenesulfonamide (W-7). These results demonstrate that forskolin exerts an hydro-osmotic effect in the mammalian nephron which occurs independent of the vasopressin receptor. Guanine nucleotide regulatory proteins may modulate the osmotic water permeability effect of forskolin. Finally, calmodulin is required for full expression of the effect of forskolin to increase osmotic water flux.