Low-temperature requirements for ascospore germination and growth of Hypoxylon diathrauston

1970 ◽  
Vol 48 (12) ◽  
pp. 2223-2225 ◽  
Author(s):  
G. B. Ouellette ◽  
E. W. B. Ward

Ascospores of Hypoxylon diathrauston Rehm germinated only at freezing temperatures or required pretreatments at −3 °C to enable them to germinate at 12 °C. They required from 10 to 30 days to germinate in our experiments. They germinated by two, but occasionally one, three, and even four, germ tubes growing through pores in the relatively thick inner wall at each end of the slit after its enlargement. Cultures grew at 0 °C with an optimum at 12–15 °C, and a maximum between 18 and 21 °C.

Plant Disease ◽  
2013 ◽  
Vol 97 (3) ◽  
pp. 323-328 ◽  
Author(s):  
Stephen C. Alderman

Epichloë typhina is an important stroma-producing endophytic ascomycete that is responsible for significant yield loss in orchardgrass (Dactylis glomerata) seed production fields. Infection is presumed to occur through leaves or stems, although details of the infection process and conditions that favor leaf infection are not well understood. The primary objectives of this study were to investigate the early stages of infection, including the effect of temperature or water potential on ascospore germination and subsequent growth of E. typhina, the tolerance of ascospores to desiccation, the requirement of leaf wounds for infection of orchardgrass by E. typhina, and the potential for insects to facilitate infection. Ascospores tolerated dry conditions, with at least 40% surviving 12 days under desiccation. Germination and growth of E. typhina was greatest at 25°C, with little to no growth at 5 and 35°C. Mycelial growth decreased with decreasing water potential from –0.3 to –10 MPa. Ascospore germination on leaves was predominantly hyphal at wound sites and iterative (conidiogenous) at sites without wounds. E. typhina typically entered leaves through wounds. Direct penetration was rarely observed and appeared to be associated with ascospore clusters. Germ tubes were significantly longer at sites with honeydew deposits from the bird cherry–oat aphid than at sites without honeydew. Growth of E. typhina was also observed at feeding sites of eriophyid mites, suggesting that leaf-wounding or sap-excreting insects support epiphyllous growth of E. typhina on leaves.


Author(s):  
Halil Tetik ◽  
Dong Lin

Abstract 3D freeze printing is a hybrid manufacturing method composed of freeze casting and inkjet-based printing. It is a facile method to fabricate lightweight, porous, and functional structures. Freeze casting is a well-known method for fabricating porous bodies and is capable of manipulating the micro-structure of the resulting product. Freeze casting simply involves solidification of a liquid suspension using low temperature and sublimation of the solvent using low temperature and pressure. After the sublimation of the solvent crystals, we obtain a porous structure where the pores are a replica of solvent crystal. Making use of the temperature gradient, as seen in unidirectional and bidirectional freeze casting, during the solidification with low temperature values, the solvent crystals grow along the temperature gradient. Furthermore, by manipulating the freezing kinetics during solidification, we can have a control on the average pore size distribution. For instance, when lower freezing temperatures result in finer pores with higher amount, higher freezing temperatures result in coarser pores with less amount. Also, the use of some additives inside the suspension leads to changes in the morphology of the solvent crystals as well as the resulting pores. However, the macro-structure of the fabricated body is highly dependent on the mold used during the process. In order to eliminate the dependency on the mold during the freeze casting process, our group recently combined this technique with inkjet-based 3D printing. With inkjet-based 3D printing, we fabricated uniform lines from single droplets, and complex 3D shapes from the lines. This provided us the ability of tailoring the macro structure of the final product without any dependency on a mold as seen in freeze casting. As a result of the 3D freeze printing process, we achieved fabricating lightweight, porous, and functional bodies with engineered micro and macro-structures. However, achieving fine droplets, and uniform lines by merging the droplets requires a good combination of fabrication parameters such as pressure adjustment inside the print head, print head speed, jetting frequency. Also, fabricating complex shapes from uniform lines requires well-adjusted parameters such as line thickness and layer height. In this study, we briefly explained the mechanics of the 3D freeze printing process. Following that we presented the development process of an open-source inkjet-based 3D printer. Finally, we explained the determination of inkjet dispensing and 3D printing parameters required for a high-quality 3D printing. During our experiments for the determination of fabrication parameters, we used a nanocellulose crystals-based ink due to its low cost and ease of preparation.


Plant Disease ◽  
1998 ◽  
Vol 82 (2) ◽  
pp. 195-202 ◽  
Author(s):  
Chuanxue Hong ◽  
Themis J. Michailides

Naturally growing apothecia of Monilinia fructicola were collected from two commercial plum orchards near Reedley and Sanger, both in Fresno County, California. Ascospore discharges from 90 (1996) and 86 (1997) apothecia were monitored individually using spore traps at four constant temperatures. The period of discharge decreased as temperature increased from 10 to 25°C. However, daily discharge increased as temperature increased from 10 to 15°C and remained high at 20 and 25°C. The greatest discharge occurred with apothecia at 15°C, followed by those incubated at 20, 10, and 25°C. The germination of ascospores of M. fructicola and the length of germ tubes increased as temperature increased from 7 to 15°C; however, increasing temperatures above 15°C did not increase either ascospore germination or length of germ tubes. This information may help in the development of warning systems and management strategies for brown rot blossom blight of stone fruits.


1955 ◽  
Vol 6 (2) ◽  
pp. 245 ◽  
Author(s):  
Y Aitken

In Trifolium subterraneum L. (subterranean clover) the low temperature requirements of its range of varieties, together with the mild winter of southern Australia, result in a lengthened growing season compared with that usual in northern Europe, and hence in greater productivity. Over much of southern Australia, some degree of summer drought prevents the use or reduces the yield of perennial species and so the productive capacity of this particular clover has made it of major importance in pastures. The low temperature requirement, however, reduces the value of the species as a self-regenerating annual where temperatures of both summer and winter seasons are too high for flower initiation. This occurs with the later varieties when sown in northern Australia. Temperatures of the summer growing season in the tropics are likely to be too high even for the short low temperature requirement of the earliest flowering group, with its high critical upper margin of about 75°F mean weekly temperature. The dry winter months are cooler, and, if water supply is available, flower initiation is possible, though retarded with consequent leafiness of the plant. Hence in northern Australia, only varieties in the early flowering group may be of use in pastures, and then only in the cooler parts of the region.


1975 ◽  
Vol 53 (1) ◽  
pp. 56-61 ◽  
Author(s):  
J. W. Paden

Ascospores of Cookeina sulcipes germinate by one of two modes: (1) by the production of blastoconidia on sympodially proliferating conidiogenous cells which may arise from any point on the spore surface, and (2) by a thick polar germ tube. No ascospores were seen to germinate both ways. The conidiogenous cells are occasionally modified into narrow hyphae. The blastoconidia germinate readily but are evidently very short-lived. Ascospores of Phillipsia crispata germinate by two polar germ tubes; there is no formation of blastoconidia. In both species the inner ascospore wall separated from an outer wall layer during germination. In culture both C. sulcipes and P. crispata form arthroconidia. The arthroconidia are uninucleate; they germinate readily and reproduce the species when transferred to fresh plates.


1988 ◽  
Vol 68 (2) ◽  
pp. 549-551 ◽  
Author(s):  
I. V. HALL ◽  
P. D. HILDEBRAND

When potted plants of lowbush blueberries were subjected to temperatures of −2 °C for periods of 0.5–4.0 h, a rosette of leaves arising from vegetative buds was induced similar to that observed in natural stands of Vaccinium angustifolium Ait. Vegetative buds at various stages of development from green tip (2 mm) to the point of leaf expansion were equally susceptible to the low temperature injury. Variation in susceptibility among seven clones tested (Brunswick, 71–14, ME-3, NB3, 895, 752, and 694) was not observed.Key words: Lowbush blueberry, low-temperature injury


1972 ◽  
Vol 50 (11) ◽  
pp. 2093-2096 ◽  
Author(s):  
Clinton F. Hodges

Germination of conidia of Curvularia geniculata from 20-, 40-, and 60-day-old cultures increased as temperature was increased to 15C. At 25C, maximum germination occurred among conidia from 20-day-old cultures, but germination from 40- and 60-day-old cultures decreased at and above 25C. Number and length of germ tubes and primary germ-tube branches increased on all conidia as temperature was increased from 5C to 25C and decreased above 25C. Germination also was influenced by culture age. Total and rate of germination decreased among conidia from older cultures at all temperatures; number and length of germ tubes and germ-tube branches also decreased on conidia from older cultures. Pathogenicity of C. geniculata was not clearly established.


1979 ◽  
Vol 57 (6) ◽  
pp. 624-628
Author(s):  
David W. Johnson ◽  
James E. Kuntz

Ascospore germination of Eutypella parasitica Dav. and Lor. occurred over a temperature range of 12 to 38 °C. Over 90% of the spores which failed to germinate at lower temperatures germinated within 24 h when placed at 24 °C. Percent germination of ascospores varied in the presence of sugar maple and red maple tissue extracts. Germination was best in the presence of outer bark, sapwood, and leaf tissue of sugar maple and red maple and was poorest in the presence of fresh inner bark tissue excised from red maple. Germ-tube development also varied with type of tissue and treatment of tissue. Long, slender, branching germ tubes developed from spores in the presence of nonsterile leaf, bark, and sapwood, whereas short, thick germ tubes developed in the presence of sterilized leaf tissue and sterilized red maple bark. Age of wounded tissue also influenced percent germination of ascospores. Generally germination was higher when pH of these tissues was greater than 5.6. Mycelial growth was best at 29 °C. Growth rate was influenced by type of medium. Both sugar maple and red maple bark incorporated into agar media had a significant inhibitory effect on diameter growth of the fungus when compared with growth on nonamended media.


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