Sporenkeimung von Phoma lingam (Tode ex. Fr.) Desm. und Resistenzprüfung bei Raps im Gewächshaus

Spore germination of Phoma lingam (Tode ex. Fr.) Desm. and methods to determine resistance of oil seed rape in the greenhouse It was the aim of this investigation to obtain more insight into the epidemiology of Phoma lingam (Tode ex. Fr.) Desm. (stat. gen. Leptosphaeria maculans (Desm.) Ces. et de Not.) and to improve the existing methods for resistance testing. In laboratory experiments the differing demands on temperature of both, the sexual as well as the non sexual phase were observed. Many ascospores developed germ tubes after eight hours at 4-8°C whilst pycnidiospores needed 24 hours at 16°C to have similar development. In greenhouse experiments young plants were infected by spraying or by placing a droplet of spore suspension onto cotyledons or leaves. Generally, ascospores were more virulent than pycnidiospores. The ascospores were obtained from old rape stalks which could be stored at -18°C without losing virulence. The most severe attack was observed after incorporating infested oat kernels (3 % w/ w) into soil, but the difference between cultivars vanished which was already low with the other methods, and which did not always correspond with results obtained in the field at stage 85, so that all these methods are not as suitable as those in the field. The distribution of pycnidiospores is also possible by adhering to the seed after threshing. The infection of the seedlings from this source was more pronounced in steamed than in unsteamed soil. The re-isolation of P. lingam increased as well from plants grown in steamed soil. Furthermore, pycnidiospores are distributed by wind during combining to neighbouring fields, already prepared at that time for rape sowing.     

Toxicity of citric and succinic acids for the pycnidiospores ofBotryodiplodia theobromae

The toxic effect of citric and succinic acids on the germination of the pycnidiospores ofBotryodiplodia theobromae, mycelial growth and the killing rate of theB. theobromae spores was investigated. The percentage inhibition of germination of viable fungal spores by 0.01% succinic or citric acid ranged between 51.6 and 58.1%, respectively.B. theobromae was found to grow in 2% malt extract broth at 28°C at the rate of 0.13 CFU/h. Citric acid exhibited a higher killing rate of 0.26 CFU/h and was more effective against the germination of the fungal spores. At concentrations of 0.3% and above, citric acid could be used as pre- and post-infectional fungicide.     

Aerated-steam treatment for control of Alter nana tenuis on lobelia seed

Alternaria tenuis may cause severe seedling blight, damping-off and leaf spotting of the bedding plant lobelia. Disease transmission from seed naturally and artificially infected by A. tenuis was demonstrated and the pathogenicity of four isolates established. Soaking of lobelia seed in 0–2% thiram suspension at 30 ^oC for 12 h adversely affected the rate of germination and did not consistently reduce infection to acceptable levels. Treatment with aerated steam at 50–51 ^oC for 15–20 min reduced seed infection to undetectable or insignificant levels and caused only slight damage to the seed. In glasshouse trials seed treated with aerated steam performed significantly better than seed soaked in thiram suspension both in terms of germination and foliage production.     

Spore germination and swarm cell morphogenesis in the acellular slime mold Fuligo septica

This report describes conditions under which spores of the acellular slime mold Fuligo septica underwent a very rapid, synchronous and complete (100%) germination followed by morphogenesis of motile, flagellated swarm cells from the released protoplasts. This developmental sequence was initiated immediately upon wetting the spores with a surfactant and was completed within 40–50 min in the absence of any exogenous nutrient other than sodium phosphate buffer. Oxygen was required for germination. The rate and percentage of germination diminished with increasing spore concentration suggesting the existence of an autoinhibitor. The morphological sequence of events in the differentiation process was examined by scanning electron microscopy.     

Persistence of <Emphasis Type="Italic">Isaria fumosorosea</Emphasis> (Hypocreales: Cordycipitaceae) SFP-198 Conidia in Corn Oil-Based Suspension

Long-term persistence of entomopathogenic fungi as biopesticides is a major requirement for successful industrialization. Corn oil carrier was superior in maintaining germination rates of Isaria fumosorosea SFP-198 conidia during exposure to 50°C for 2 h, when compared with other oils, such as soybean oil, cottonseed oil, paraffin oil, and methyl oleate. The corn oil-based conidial suspension (91.6% germination) was also better in this regard than conidial powder (28.4% germination) after 50°C for 8 h. Long-term storage stabilities of corn oil-based conidial suspension and conidial powder at 4 and 25°C for 24 months were investigated, based on the correlation of germination rate with insecticidal activity against greenhouse whiteflies, Trialeurodes vaporariorum. Viability of conidia in corn oil was more than 98.4% for up to 9 months of storage at 25°C, and followed by 23% at 21 months. However, conidial powder had only 34% viability after 3 months of storage at 25°C, after which its viability rapidly decreased. The two conidial preparations stored at 4°C had better viabilities than those at 25°C, showing the same pattern as above. These results indicate that corn oil-based conidial suspension can be used to improve conidial persistence in long-term storage and be further applied to the formulation of other thermo-susceptible biological control agents.     

Effect of high temperatures on seed germination of two woody Leguminosae

Cytisus scoparius and Genista florida regenerate after fire by stump-sprouting but also by seed. Seeds of these species were heated to a range of temperatures similar to those registered on the surface soil during natural fires (from 50 to 150 °C) and a range of exposure times (from 1 to 15 min). No germination was observed at high temperatures, 130 °C, when the exposure time was 5 min or more. However, moderate heat treatments (at 70 and 100 °C) significantly increased the rate of germination relative to controls. Cytisus scoparius is more favoured by fire action than Genista florida, with germination rates slightly greater following 100 °C for 5 min and 130 °C for 1 min than after mechanical scarification.     

Activity of Azole Fungicides and ABC Transporter Modulators on Mycosphaerella graminicola

The antimicrobial activity of the azole fungicides cyproconazole and propiconazole as single active ingredients and in mixtures with the ATP-Binding Cassette (ABC) transporter modulators rhodamine 6G, quercetin, quinidine, and verapamil and the strobilurin kresoxim-methyl was assessed against the wheat pathogen Mycosphaerella graminicola . Interactions amongst these compounds were evaluated on germination and germ tube growth of pycnidiospores using the Colby and Wadley method. Water agar proved to be the best test medium since all pycnidiospores germinated within 24 h of incubation and apical germ tube growth dominated over bud formation by intermediate cells. Analysis with the Colby method revealed that interactions between the compounds in all mixtures tested on germination of pycnidiospores were additive. With regard to germ tube growth, mixtures of cyproconazole and verapamil or kresoxim-methyl displayed a synergistic interaction. Analysis of mixtures of cyproconazole and kresoxim-methyl with the Wadley method revealed that the interaction between the two compounds was purely additive. These results indicate that the Colby method overestimated the interaction between these two compounds in a mixture.     

Factors Affecting Germination and the Mode of Germination of Zygospores of Choanephora cucurbitarum

Treatment of zygospores of Choanephora cucurbitarum with KMnO₄, NaClO or H₂O₂ effectively activated the spores and induced their germination. The optimum concentration of KMnO₄ for activation of zygospores was 0.25 to 0.5%. Zygospores were not able to germinate in darkness even after activation by KMnO₄. When zygospores from 40 to 50-day-old cultures were treated with 0.5% KMnO₄ solution for 60 min before incubation on water agar at 24% under light, about 50% germinated in 10 days. KMnO₄ treatment killed more than 99% of residual mycelial fragments, sporangiospores and sporangiola in the zygospore suspension. During germination disappearance of oil droplets in zygospores occurred prior to the cracking on zygospore wall. Both sporangial germination and mycelial germination were found. Moreover, sporangiole germination was observed for the first time.     

Factors influencing pathogenicity of Fusarium tumidum on gorse (Ulex europaeus)

Factors promoting pathogenicity of Fusarium tumidum on gorse (Ulex europaeus) were determined to develop a novel strategy for delivering this potential mycoherbicide using insects as vectors of inoculum. Fusarium tumidum sprayed as a suspension of 1×10⁶ conidia mL^?1 on at least 50% of a gorse plant reduced shoot dry weight by 45% (P<0.05). A minimum of 910 viable conidia were required to cause a lesion on leaves. The leaves and flowers were more susceptible to infection than stems, spines and pods. Generally, wounding of gorse leaves and stem increased F. tumidum infection, most likely through releasing nutrients that enhanced conidial germination and hyphal growth. We showed in a separate experiment that conidial germination (93%) and germ tube length (407 µm) were greater when incubated in 0.2% gorse extract solution for 24 h than in water (62% germination, germ tube length 42 µm). Inoculation of gorse with a F. tumidum conidial suspension supplemented with 0.2% gorse extract resulted in a shoot dry weight reduction (P=0.012) equivalent to that of plants that were wounded and inoculated. It is concluded that wounding of older tissues (which mimics insect damage) is required to facilitate F. tumidum infection of mature gorse plants.     

Burial of canopy-stored seeds in the annual psammophyte Agriophyllum squarrosum Moq. (Chenopodiaceae) and its ecological significance

Agriophyllum squarrosum Moq. is a dominant annual on sand dunes in the arid regions of central Asia. A high percentage of seeds is retained on dead plants which become covered by moving sand, but little is known about the ecological significance of burial of canopy-stored seeds. We investigated the size and dynamics of the buried canopy-stored seed bank and effects of burial on seed germination. In March (during the windy season), May (beginning of the germination season), and July (middle of the growing season), the number of seeds per square meter in sample plots in the dunes was 623, 223 and 22, respectively, with 54.6, 30.6 and 12.9% of the total seeds retained on buried plant canopies. In a controlled experiment, more seedlings emerged from released (dispersed) than from canopy-stored seeds when burial depth was the same. No viable ungerminated released seeds were found, but 45–80% of the ungerminated canopy-stored seeds were viable. In general, with an increase in applied water germination of released seeds buried at a depth of 1 or 2 cm and of canopy-stored seeds buried at 1 cm increased, but regardless of watering regime few or no released seeds at 4 cm or canopy-stored seeds at 2 or 4 cm germinated. Significantly more seedlings emerged from plants buried in a horizontal than in a vertical position. Seedlings originating from buried canopy-stored seeds on an active dune accounted for only 5.4% of the total seedlings emerging, and most of them emerged later than those from released seeds. Thus, seed release is more effectively postponed in buried than in exposed canopies, and burial of canopy-stored seeds is a mechanism that helps regulate seed germination and seedling emergence of A. squarrosum on active dunes.     

Stimulation der Keimung von Kiefernpollen durch UV-Bestrahlung

Zusammenfassung Bei der Aufnahme der Dosis-Effekt-Kurve für die Keimung vonPinus-Pollen nach UV-Bestrahlung in Suspension (etwa 0,4 mW/cm², 265 nm) findet man bis zu 1,5 min Bestrahlungszeit eine deutliche Stimulation des Keimvorganges.

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Stimulation of the germination of Pine Pollen by ultra-violet irradiation

Summary When investigating the dose-effect-curve of the germination of pine pollen after uv irradiation in suspension (approx. 0.4 mW/cm²,265 nm) one gets a significant stimulation of the germination process up to 1.5 min of irradiation.

     

Tomato Seed Germination. Osmotic Pretreatment and Far Red Inhibition

At 25 °C germination of tomato (Lycopersicon lycopersicum)seeds is inhibited by continuous and intermittent far red illumination.It is also inhibited by a single 30 min far red irradiationgiven 8 h from the start of imbibition. The incubation of seedsin a mannitol solution inhibitory for germination has no effecton the final germination percentage after seeds are subsequentlytransferred to water. A 30 min far red irradiation at the timeof transfer results in partial inhibition of germination. Thisinhibition can be released by the continuation of osmotic incubationfor several days before the transfer to water. At the end ofa 7 d dark period of osmotic incubation, inhibition of subsequentgermination in water can be realized only by continuous farred illumination. Seeds osmotically pretreated for 7 d and afterwardsdried-back show a mean time to 50% germination significantlylower than that of untreated seeds. Moreover, besides singleand intermittent, even continuous far red light has no inhibitoryeffect on the germination of these seeds. It is concluded that,in addition to the already known germination advantages, osmoticpresowing treatment also induces the ability of seeds to germinateunder unfavourable light conditi.     

A rapid screening method for the detection of viable spores in powder using bioluminescence.

A rapid diagnosis of a biological threat in a powder sample is important for fi rst responders who have to make decisions on-site. The present culture-based method does not provide timely results, which is a critical barrier for a quick response when a suspicious powder sample is found. The ATP bioluminescence method, combined with a heat shock, was investigated to determine the presence of spores in powder. The results show that only spore-containing powder samples provided a dramatic increase in the bioluminescence signal after the heat shock, which induces germination of the spores. Various conditions were tested to fi nd the most effective and rapid germination procedure. Elevated temperatures (37 degrees C and 50 degrees C) were more effective in germination than room temperature. At 50 degrees C, a double-strength germinant was more effective in germination than the regular strength. The 37 degrees C/15 min procedure induced the germination of spores most effectively, while a 50 degrees C/2 min procedure provided reasonably high signals, so it could make the entire procedure even faster (< 5 min). The detection limit of the bioluminescence method is < 100 spores.     

Effect of hot-water treatments in vitro on conidial germination and mycelial growth of grapevine trunk pathogens

In this study, the sensitivity of Cadophora luteo-olivacea, Cylindrocarpon liriodendri, Cn. macrodidymum and eight species of the genus Phaeoacremonium to hot-water treatments (HWTs) in vitro was evaluated. Conidial suspensions and plugs of agar with mycelia were placed in Eppendorf vials and incubated for 30, 45 or 60 min in a hot-water bath at 41, 42, 43, 44, 45, 46, 47, 48 or 49°C for Cylindrocarpon spp. and at 49, 50, 51, 52, 53, 54 or 55°C for Ca. luteo-olivacea and Phaeoacremonium spp. In general, conidial germination and the colony growth rate of all pathogens decreased with increased temperature and time combinations. Cylindrocarpon spp. were more sensitive than Ca. luteo-olivacea and Phaeoacremonium spp. to HWT temperatures. Conidial germination of Ca. luteo-olivacea was inhibited by treatments above 51°C–30 min, while treatments up to 54°C–60 min were necessary to inhibit the mycelial growth. For Cylindrocarpon spp., conidial germination was inhibited by treatments above 45°C–45 min, while treatments above 48°C–45 min were necessary to inhibit the mycelial growth. Regarding Phaeoacremonium spp., treatments up to 54°C–60 min were necessary to completely inhibit both conidial germination and mycelial growth. These results suggest that current HWT protocols at 50°C for 30 min may be sufficient to control Cylindrocarpon spp. However, it would be necessary to develop HWT using higher temperatures to reduce the incidence of Ca. luteo-olivacea and Phaeoacremonium spp. infections.     

FREE AMINO ACID CHANGES DURING GERMINATION OF TELIOSPORES OF THE WHEAT BUNT FUNGUS,TILLETIA CARIES

Teliospores were aerated and agitated in a mineral salts medium and their free amino acid contents were analyzed at eight different times, from shortly after imbibition of water until just before germ tube emergence. In addition to the common amino acids, eight unidentified ninhydrin-positive components were detected. About 50 % or more of nearly each of the amino acids diffused out of the spores during the initial phase of germination. These released amino acids were actively taken up by the spores during the latter stages of germination. The free amino acids in largest amounts in the dormant spores of T. caries were arginine 15.0, glutamic acid 6.3, and alanine 3.7 μmoles per g dry spores. Together these three amino acids accounted for about 71 % of the total free amino acids in dormant spores of T. caries and T. controversa. The total amounts of free amino acids in spores of common bunt were much higher than in spores of dwarf bunt.     

Heat shock effects on seed germination of five Brazilian savanna species

Fire is considered an important factor in influencing the physiognomy, dynamics and composition of Neotropical savannas. Species of diverse physiognomies exhibit different responses to fire, such as population persistence and seed mortality, according to the fire frequency to which they are submitted. The aim of this study is to investigate the effects of heat shocks on seed germination of Anadenanthera macrocarpa (Benth.) Brenan, Dalbergia miscolobium Benth., Aristolochia galeata Mart. & Zucc., Kielmeyera coriacea (Spreng.) Mart. and Guazuma ulmifolia Lam., which are native species of the Brazilian savanna. The temperatures and exposure times to which the seeds were submitted were established according to data obtained in the field during a prescribed fire: 60 °C (10, 20 and 40 min), 80 °C (5, 10 and 20 min) and 100 °C (2, 5 and 10 min). Untreated seeds were used as controls. Seeds of A. galeata and K. coriacea showed high tolerance to most heat treatments, and seeds of A. macrocarpa showed a significant reduction in germination percentage after treatments of 80 °C and 100 °C. Treatments of 100 °C for 10 min reduced germination percentage for all species except G. ulmifolia, which has dormant seeds. For this species, germination was accelerated by heat treatments. The high temperatures applied did not interfere with the time to 50% germination (T₅₀) of the tolerant seeds. Seeds of the savanna species K. coriacea and A. galeata were more tolerant to heat shocks than seeds of the forest species A. macrocarpa. Guazuma ulmifolia, the forest species with seeds that germinate after heat shock, also occurs in savanna physiognomies. Overall, the high temperatures applied did not affect the germination rate of the tolerant seeds.     

Dispersal of Septoria nodorum Pycnidiospores by Simulated Rain and Wind

The influence of wind on the splash dispersal of Septoria nodorum pycnidiospores was studied in a raintower/wind tunnel complex with single drops or simulated rain falling on spore suspensions or infected stubble with windspeeds of 1.5 to 4 m/sec. When single drops fell on spore suspensions (depth 0.5 mm, concentration 7.8 × 10⁵ spores/ml) most of the spore-carrying droplets collected on fixed photographic film between 0–4 m downwind (windspeed 3 m/sec) were >200 μm in diameter. However, most spores were carried in droplets with diameter > 1000 μm, 70 % of which carried more than 100 spores. When simulated rain fell on infected stubble most of the spore-carrying droplets collected beyond 1 m downwind (windspeeds 1.4 and 4 m/sec) were <200 μm in diameter and none were >600 μm; most of these droplets carried only one spore. The distribution of splash droplets (with diameter >100 μm) deposited on chromatography paper showed a maximum at 40–50 cm upwind of the target but many more droplets were deposited 20–30 cm downwind, when single drops fell on a spore suspension (concentration 1.2 × 10⁵ spores/ ml) containing fluorescein dye with a windspeed of 2 m/sec; droplets were collected up to 3 m downwind but not more than 70 cm upwind. With a windspeed of 3 m/sec, numbers of sporecarrying droplets and spores collected on film decreased with increasing distance downwind; most were collected within 2 m of the target but some were found up to 4 m. When simulated rain fell on infected stubble, increasing the windspeed from 1.5 to 4 m/sec greatly increased the number of spores deposited more than 1 m downwind. At 1.5 m/sec none were collected beyond 2 m downwind, whereas at 4 m/sec some were collected at 4 m. A few air-borne S. nodorum spores were collected by suction samplers at a height of 40 cm at distances up to 10 m downwind of a target spore suspension on which simulated rain fell.     

Ca2+ regulation of Phyllosticta ampelicida pycnidiospore germination and appressorium Formation

Phyllosticta ampelicida conidia germinate only after making contact with and attaching to a substratum. Previous studies suggested a role for Ca2+ in this process. A Ca2+ buffering system was used to control the external free Ca2+ concentration. Both germination and appressorium formation were reduced or abolished with low Ca2+ (less than or equal to nanomolar levels) but were nearly 100% at millimolar levels of Ca2+. Germination initiation required Ca2+ within 10-25 min after the spore made contact with the substratum. Appressorium initiation required Ca2+ 90-120 min following initial contact. Ca2+ channel blockers nicardipine and lanthanum abated spore development. TMB-8, a blocker of internal Ca2+ channels, reduced both developmental events. Gadolinium, a putative stretch-activated Ca2+ channel blocker, abolished both developmental events at nanomolar levels. Calmodulin antagonists, compounds R-24751 and 48/80, abated spore development at micromolar levels. Together, these results suggest that Ca2+ signaling is involved in both germination and appressorium formation in P. ampelicida pycnidiospores.     

Germination of concentrated suspensions of spores from Aspergillus niger

Summary Germination of condiospores fromA.niger in very concentrated suspension was required to inoculate solid fermentation media, but a germination self-inhibitor was detected in spores. It was found that the inhibitory effect depended on the composition of the medium and was reduced when glucose was used as a carbon source. The effect of the self-inhibitor was eliminated by washing the spores and using glucose and a protein nitrogen source in the germination medium. By this method it was possible to increase about 100 times (10⁶ to 10⁸) spore concentration, keeping more than 90% germination.     

The significance of temperature during sporulation on the biology of pycnidiospores of Mycosphaerella ligiilicola

The germination, infectivity and survival of pycnidiospores obtained from cultures of Mycosphaerella ligulicola grown at 15 and 26 °C were compared. Spores formed at 26° (‘26° spores’) were less able to germinate at low relative humidities and showed a narrower temperature range for maximum germination after 6 h. At high spore densities 26° spores showed self-inhibition of germination and, over a range of lower densities, growth of their germ tubes was checked, which resulted in lower infection of leaf discs compared with 15° spores in which this phenomenon did not occur. The fungus could be recovered from un-sterile compost over a longer period after inoculation with 15° spores. Only after storage at a temperature well below zero was there a difference in viability between 15° and 26° spores. It is thought that the potential advantage of producing larger numbers of spores at 26° would be realized only under optimum conditions for dispersal and infection. The smaller number of spores produced at 15° are likely to be successful under natural conditions.