Articles by Taxonomic Group

New records of microfungal genera from Mt. Strandzha in Bulgaria (south-eastern Europe). II
Elşad Hüseyin, Faruk Selçuk & Ali S. Bülbül
Mycologia Balcanica 8: 157–160 (2011)
doi: https://doi.org/10.5281/zenodo.2550707
Published online: 13 December 2011
Download PDF
Abstract
Show abstract
Keywords
Show keywords

Twenty species of ascomycetous and anamorphic fungi from twenty genera are reported for the first time from Mt. Strandzha in Bulgaria.

Pezizomycotina, anamorphic fungi, Bulgaria, fungal diversity, Mt. Strandzha
The hypogeous fungi from Sicily (southern Italy): new additions
Alessandro Saitta, Maria L. Gargano, Marco Morara, Mirko Ilice & Giuseppe Venturella
Mycologia Balcanica 5: 147–152 (2008)
doi: https://doi.org/10.5281/zenodo.2548806
Published online: 23 December 2008
Download PDF
Abstract
Show abstract
Keywords
Show keywords

The distribution and ecology of forty hypogeous fungi from Sicily (southern Italy) is here pointed out. Hysterangium stoloniferum, Protoglossum aromaticum, Sclerogaster compactus and Tuber maculatum are reported as new records from Sicily. Gymnomyces xanthosporus and Melanogaster umbrinigleba are also new for Italy.

distribution, ecology, hypogeous fungi, Sicily
Adaptive growth rates of fungi from Aspergillus niger group in contrasting environments: the Dead Sea and "Evolution Canyon" I (Israel) under different osmostress
Katerina Selezska, Leonid Brodsky & Eviatar Nevo
Mycologia Balcanica 4: 51–60 (2007)
doi: https://doi.org/10.5281/zenodo.2547759
Published online: 20 June 2007
Download PDF
Abstract
Show abstract
Keywords
Show keywords

Filamentous fungi from Aspergillus niger group were isolated from the hypersaline Dead Sea water 
and the Mediterranean “Evolution Canyon” I, lower Nahal Oren, Mount Carmel. A comparison of growth rates of the strains collected from the Dead Sea and the “European” north- and “African” south-facing slopes of “Evolution Canyon” I, over a range of water activities, was provided. Media adjustments were made with different volumes of Dead Sea water. Strains from all habitats showed optimal growth rates at 5 % of Dead Sea water (aw 0.983) and ceased growth at 65 % of Dead Sea water (0.785 aw). However, significant interpopulation growth differences were detected (by the non-parametric Kolmogorov-Smirnov test) at different aw. Under low salinities (< 15 %), “Evolution Canyon” I strains significantly differ from Dead Sea water strains in distributions of growth rates. Under high salinities (> 40 %), there is the same divergence of “Evolution Canyon” I strains vs. Dead Sea water strains, and some divergence between “African” and “European” slopes appears. “African” slope and “European” slope populations are significantly different in growth rates under 40 % salinity and have a tendency to be different under 45 % and 50 % volumes of Dead Sea water. We conclude that the A. niger group isolated from the Dead Sea water is more resistant, and the “African” slope population has a tendency to be more resistant than the “European” slope to stress associated with low-water activity. We suppose that these patterns are adaptive.

Aspergillus niger group, Dead Sea water, growth rate, water activity stress