Nectria tuberculariformis, Nectriella muelleri, Nectriella sp., and Hyponectria sceptri: low-temperature tolerant, alpine–boreal fungal antagonists

1984 ◽  
Vol 62 (9) ◽  
pp. 1896-1903 ◽  
Author(s):  
G. J. Samuels ◽  
C. T. Rogerson ◽  
A. Y. Rossman ◽  
J. D. Smith

The ascomycetes Nectria tuberculariformis, Nectriella muelleri sp. nov., Nectriella sp., and Hyponectria sceptri comb. nov. were collected in alpine–boreal habitats. They were low temperature tolerant, growing at 0 °C and poorly or not at all at temperatures above 18 °C. Optimum temperature for spore germination and growth was 10–15 °C. Nectria tuberculariformis was found to be the teleomorph of Acremonium boreale; Nectriella muelleri and Nectriella sp. each had Acremonium anamorphs. No anamorph formed in cultures of Hyponectria sceptri. All four species produced a diffusible substance or substances that inhibited growth of the mesophilic plant parasites Chondrostereum purpureum, Fusarium solani, Glomerella cingulata, and Phoma medicaginis var. pinodella. Nectria tuberculariformis, Nectriella muelleri, Nectriella sp., and Hyponectria sceptri are described and illustrated.

1972 ◽  
Vol 18 (7) ◽  
pp. 975-979 ◽  
Author(s):  
B. W. Streets ◽  
M. B. Ingle

Mucor miehei was grown in submerged culture at 30, 37, 40, 42.5, 45, and 48 °C. Maximum growth yield occurred at 48 °C.The effect of temperature on spore germination was examined. No spores germinated within 8 h at temperatures below 36.7 °C or above 53.5 °C. The optimum temperature for spore germination was 45 °C.Growth occurred at the marginal temperatures of 20 °C and 25 °C only when the spores were pre-germinated at 37 °C


1983 ◽  
Vol 46 (2) ◽  
pp. 135-141 ◽  
Author(s):  
LARRY R. BEUCHAT

The behavior of yeasts and molds as influenced by water activity (aw) is reviewed. Fungal spoilage of foods occurs more often than bacterial spoilage at aw 0.61–0.85 not because fungi grow faster at reduced aw but rather because the competitive effects of the vast majority of bacteria are absent. Higher aw is generally required for spore formation than for spore germination. The range of aw permitting germination of spores is greatest at an optimum temperature, but optimum availability of nutrients tends to broaden the range of aw and temperature at which germination and growth will occur. The minimum aw levels for growth of fungi are lower than those required for mycotoxin production. It is imperative that diluents and enumeration media with reduced aw be used to detect xerotolerant fungi in foods. Otherwise, vegetative cells and spores may be killed by osmotic shock or remain dormant when exposed to high aw associated with diluents and media routinely used for mycological analyses.


Food Research ◽  
2019 ◽  
pp. 808-813
Author(s):  
Ubong A. ◽  
C.Y. New ◽  
L.C. Chai ◽  
Nur Fatihah A. ◽  
Nur Hasria K. ◽  
...  

Bacillus cereus spores are capable of surviving the harsh environment and more often, they cause great concern to the dairy industry. The current research was conducted to study the effect of temperature on germination and growth of B. cereus spores in UHT chocolate milk; the study was carried out at 8°C, 25°C and 35°C over a span of seven days. The results showed that no growth was observed at 8°C. At 25°C, a rapid increase in growth was observed as early as Day 1, from an initial count of ten spores to 4.01 log10 CFU/mL. Meanwhile, at 35°C, the growth on Day 1 was more rapid in which the count promptly increased to 8.07 log10 CFU/mL. Analysis of graph trend showed that the number of vegetative cells decreased while the number of spores increased with incubation time due to nutrients exhaustion. This study fills up the data gap towards understanding the possible issues that might arise in the actual scenario and at the same time, suggests a suitable approach to minimize infection risk caused by B. cereus spores.


2019 ◽  
Vol 2 (1) ◽  
pp. 16
Author(s):  
Aprisianus Julkarman Simbolon ◽  
Ganjar Adhywirawan Sutarjo ◽  
Hariyadi Hariyadi

Cantikgrouper is the hybridization results grouper or cross-breeding between Epinephelus fuscoguttatus as a female and Epinephelus microdon as a male. The main barriers faced in the development of this commodity is still low levels of spawning up to seeding grouper. Based on the background, this study aimed to investigate optimum temperature observations against the rate of embryonic development Epinephelus sp.larvae. This study used the results of artificial spawning eggs.The fertilized eggs were incubated on six pieces of the container temperature treatment;each treatment there was repeated three times.The incubation temperature was kept on (A) 21-22°C; (B) 23-24°C; (C) 25-26°C; (D) 27-28°C; (E) 29-30°C; (F) 31-32°C. Results showed that eggswere incubated at a temperature of 21-22 ℃ embryonic development to a halt in the blastula, and temperature 23-24°C stalled on phasemyomere embryos. The low-temperature incubation period lasts a long time. Temperature 25-26°C needed 18 hours 6 minutes by 8.33% abnormality rate. Temperature 27-28°C needed 16 hours to hatch witha degree of abnormality of 7.6%. Temperature 29-30°C needed 15 hours 1 minute for the hatch tothe degree of abnormality of 5.33%. The 31-32°C temperature needed 14 hours 6 minutes to hatch witha degree of abnormality of 17.3%. The limits of tolerance for the incubation of the eggs ofcantik grouper (Epinephelusspp.) were 26-32°C.The best temperature of each treatment were obtained at a temperature of 29-30°C. Based on our results, it concluded that the changing temperature affected how long eggs could hatch.


1978 ◽  
Vol 26 (1) ◽  
pp. 110-118
Author(s):  
J. de Jong

Rooted cuttings of commercial cvs were grown to flowering at five temperatures and the the number of short days to flowering was recorded. The optimum temperature for rapid flowering varied between cvs. The number of days to flowering at the optimum temperature was not related to the delay in flowering caused by either high or low temperature. In many cvs the delay in flowering at low temperature was accompanied by a similar delay at high temperature. It was concluded that for the character 'time to flowering' genotypes should preferably be selected at low temperatures. If low temperature cannot be realized, only rapidly flowering genotypes should be selected. (Abstract retrieved from CAB Abstracts by CABI’s permission)


1963 ◽  
Vol 50 (8) ◽  
pp. 806-814 ◽  
Author(s):  
Vincent W. Cochrane ◽  
Jean Conn Cochrane ◽  
Calden B. Collins ◽  
Frank G. Serafin

Life ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 1 ◽  
Author(s):  
Wayne L. Nicholson ◽  
Antonio J. Ricco

We report here complete 6-month results from the orbiting Space Environment Survivability of Living Organisms (SESLO) experiment. The world’s first and only long-duration live-biology cubesat experiment, SESLO was executed by one of two 10-cm cube-format payloads aboard the 5.5-kg O/OREOS (Organism/Organic Exposure to Orbital Stresses) free-flying nanosatellite, which launched to a 72°-inclination, 650-km Earth orbit in 2010. The SESLO experiment measured the long-term survival, germination, metabolic, and growth responses of Bacillus subtilis spores exposed to microgravity and ionizing radiation including heavy-ion bombardment. A pair of radiation dosimeters (RadFETs, i.e., radiation-sensitive field-effect transistors) within the SESLO payload provided an in-situ dose rate estimate of 6–7.6 mGy/day throughout the mission. Microwells containing samples of dried spores of a wild-type B. subtilis strain and a radiation-sensitive mutant deficient in Non-Homologoous End Joining (NHEJ) were rehydrated after 14, 91, and 181 days in space with nutrient medium containing with the redox dye alamarBlue (aB), which changes color upon reaction with cellular metabolites. Three-color transmitted light intensity measurements of all microwells were telemetered to Earth within days of each 24-hour growth experiment. At 14 and 91 days, spaceflight samples germinated, grew, and metabolized significantly more slowly than matching ground-control samples, as measured both by aB reduction and optical density changes; these rate differences notwithstanding, the final optical density attained was the same in both flight and ground samples. After 181 days in space, spore germination and growth appeared hindered and abnormal. We attribute the differences not to an effect of the space environment per se, as both spaceflight and ground-control samples exhibited the same behavior, but to a pair of ~15-day thermal excursions, after the 91-day measurement and before the 181-day experiment, that peaked above 46 °C in the SESLO payload. Because the payload hardware operated nominally at 181 days, the growth issues point to heat damage, most likely to component(s) of the growth medium (RPMI 1640 containing aB) or to biocompatibility issues caused by heat-accelerated outgassing or leaching of harmful compounds from components of the SESLO hardware and electronics.


Weed Science ◽  
1987 ◽  
Vol 35 (4) ◽  
pp. 519-523 ◽  
Author(s):  
David R. Shaw ◽  
H. Randy Smith ◽  
A. Wayne Cole ◽  
Charles E. Snipes

The optimum pH for germination of smallflower morningglory (Jacquemontia tamnifolia(L.) Griseb. # IAQTA] seed was 8.0. A scarification time of 25 to 60 s using a drum scarifier with medium grit provided the best germination, and the optimum temperature for germination was 35 to 40C. However, the optimum temperature for growth was 25 to 35C, with reductions in growth occurring above or below this range. Emergence after 14 days was 81 and 49% at planting depths of 1.5 and 10 cm, respectively. Shade levels of 30 to 92% reduced smallflower morningglory growth by 38 to 87% compared to plants grown in full sunlight.


2007 ◽  
Vol 97 (12) ◽  
pp. 1600-1607 ◽  
Author(s):  
Antonio Trapero-Casas ◽  
Walter J. Kaiser

Studies were performed to compare the germination and infection of ascospores and conidia of Didymella rabiei under different temperature and moisture conditions. Germination of ascospores and conidia on cover glasses coated with water agar began after 2 h, with maximum germination (>95%) occurring in 6 h at 20°C. No germination occurred at 0 and 35°C. Ascospores germinated more rapidly than conidia at all temperatures. Germination declined rapidly as the water potential varied from 0 to –4 MPa, although some germination occurred at –6 MPa at 20 and 25°C. Ascospores germinated over a wider range of water potentials than conidia and their germ tubes were longer than those of conidia at most water potentials and temperatures. The optimum temperature for infection and disease development by both ascospores and conidia was around 20°C. Disease severity was higher when ascospores were discharged directly onto plant surfaces from naturally infested chickpea debris compared with aqueous suspensions of ascospores and conidia sprayed onto plants Disease severity increased as the length of the wetness period increased. When dry periods of 6 to 48 h occurred immediately after inoculation, disease severity decreased, except for the shorter periods which had the opposite effect. Disease severity was higher with ascospore inoculum when no dry periods occurred after inoculation.


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