scholarly journals A Modified Double Subculture Method for the Two-Mode Injuries Evaluation in a Stressed Fungal Spore Population

2020 ◽  
Vol 25 (3) ◽  
pp. 131-138
Author(s):  
SHIGETOSHI HORIKIRI ◽  
MASAKAZU FURUTA ◽  
TETSUAKI TSUCHIDO
2016 ◽  
Vol 2016 (4) ◽  
pp. 19 ◽  
Author(s):  
Raghda K. Fayad ◽  
Mohammed H. Abu-Dieyeh

2021 ◽  
Vol 8 (2) ◽  
pp. 49-60
Author(s):  
Santhoshkumar S ◽  
Devaraj D

The present study to investigate the arbuscular mycorrhizal fungal root colonization and spore population of some medicinal plants species at Theerthamalai hills Western Ghats of Dharmapuri district, Tamil Nadu. Root and rhizosphere soil samples were collected during the month of August, 2010-March, 2011. From the surface to 20 cm depth as well as pH were also measured. Totally 42 plant species belonging to 24 families recovered Arbuscular mycorrhizal fungal spore and root colonization. The results of the present study arbuscular mycorrhizal fungal spore population in the rhizosphere soil and root colonization of all the plant species. The maximum spore population was found in the rhizosphere soil samples of the plant species Leucas aspera (386/100g of soil) which belongs to the family Lamiaceae and lowest spore population was observed in the  Wrightia tinctoria (117/100g of soil) belongs to Apocyanaceae. The maximum AM fungal infection was found in roots of Cassia auriculata (63%) belongs to the family Fabaceae, while the lowest AM fungal association was found in the root of Achyranthes aspera (17%) belongs to the family Amaranthaceae. A total of 24 AM fungal species belonging to 4 genera were recorded from the rhizosphere soil samples of this study region. Among these genus Glomus was dominant had seen in rhizosphere soil samples in all the medicinal plant species.


Author(s):  
Raghdaa K. Fayad ◽  
Roda F. Al-Thani ◽  
Fatima A. Al-Naemi ◽  
Mohammed H. Abu-Dieyeh

This research was conducted to investigate the dynamics of airborne fungi using viable culture collection and in respect to different abiotic variables, including seasonal and intra-diurnal variations. A gravimetric method was used to sample airborne fungal deposition on potato dextrose agar plates on alternate days, for a year between April 2015 to March 2016. From 176 settle plate exposures, a total of 1197 mould and 283 yeast colony-forming units (CFU), 21 genera and 62 species were retrieved. The highest fungal spore count was recorded in February 2016, whereas the lowest count occurred in August 2015. The main constituents of the fungal airspora were attributed to Cladosporium (60.2%), Aspergillus (10.4%), Fusarium (9.4%), Alternaria (8.5%), and Ganoderma spp. (2.3%). Temperature was negatively correlated with total colony count (r = −0.231, p ≤ 0.05) or species richness (r = −0.267, p ≤ 0.001), while wind speed was positively correlated with total colony count (r = 0.484, p ≤ 0.001) or species richness (r = 0.257, p ≤ −0.001). The highest dispersal of fungal spores was obtained at 18:00, whereas the lowest fungal spores release was recorded at 00:00 (midnight). There were no significant differences in species composition and richness of the airborne fungal population between two study sites, the Industrial area and Qatar University Campus. The count of Alternaria spp. and Fusarium spp. were significantly higher at the Industrial area site, which corresponds to a higher CO2 level than the Qatar University site. This study lays the foundation for future work to assess the implications of such aeromycological data on public health.


1977 ◽  
Vol 23 (9) ◽  
pp. 1170-1177 ◽  
Author(s):  
David A. Cotter

Polyalcohols such as ethylene glycol and glycerol at 3 M penetrate and activate spores of Dictyostelium discoideum incubated at room temperature. Higher concentrations of ethylene glycol result in lysis upon suspension of spores in dilute phosphate buffer. Erythritol and arabitol at 3 M do not penetrate or activate D. discoideum spores.Air-dried spores or those incubated in 2 M sucrose solutions are not activated with the usual heat treatment of 45 °C for 30 min. The plasmolyzed spores are activated at temperatures above 45 °C when heated in the presence of 2 M sucrose for 30 min. The temperature for maximum activation and the temperature for thermal inactivation of spores are raised 7–10 °C in high sucrose concentrations. Long-term incubation of heat-activated spores in 2 M sucrose solutions does not result in a return to dormancy.Moderate sucrose concentrations near 0.2 M do not block the heat-induced activation process but must be removed from the spore population to prevent a return to dormancy within 6 h. Other polyhydric compounds at 0.25 M concentration also cause spore deactivation within 6 h of room temperature incubation. Oxygen uptake of spores undergoing deactivation in 0.18 M sucrose is inhibited as compared to control levels. Moderate concentrations of sucrose do not block the early events of postactivation lag and the spores accumulate at the end of the lag phase. The longer the spores remain unswollen at the end of the postactivation lag phase, the greater the percentage of spores which return to dormancy. The effects of moderate sucrose concentration (lowered water activity) are not duplicated by the same quantity of Ficoll, indicating that the colligative properties of the sucrose solutions are responsible for deactivation.


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