Selected detrimental and essential elements in fruiting bodies of culinary and toxic medicinal macroscopic fungi growing in the Bohemian Forest, the Czech Republic.

Selected wild-growing edible fungi (Boletus edulis, Neoboletus luridiformis, Cantharellus cibarius, Macrolepiota procera, Amanita rubescens, Russula virescens, Lycoperdon perlatum, and Flammulina velutipes) along with the poisonous medicinal species Amanita muscaria were collected from five sites in the Bohemian Forest, the Czech Republic and analyzed regarding the contents of 19 elements (Ag, Al, As, Be, Ca, Cd, Co, Cr, Cu, Fe, Li, Mg, Mn, Ni, Pb, Rb, Se, Tl, and Zn) in their fruiting bodies. The contents of the elements as well as bioconcentration factors (ratios of the element content in dry matter of the mushroom to the content in the soil; BCF) were significantly species dependent. In general, the analysis revealed the most intensive accumulation of Cd, Rb, Ag, Cu, Se, and Zn in the studied mushrooms. B. edulis accumulated Ag, Se, Cd, Rb, Cu, and Zn with average BCF of 31, 25, 18, 13, 3.9, and 2.6, respectively. On the other hand, A. rubescens accumulated Cd, Rb, Ag, Cu, Zn, and As (BCF of 41, 27, 4.8, 3.3, 2.1, and 1.4). The data concerning the detrimental elements in sporocarps of edible mushrooms indicate no negative effect on human health if the fungi are consumed occasionally or as a delicacy.

Detrimental and essential elements in fruiting bodies of mushrooms with ecological relationship to birch (Betula sp.) collected in the Bohemian Forest, the Czech Republic.

Four macrofungi species with ecological relationship to birch (Betula sp.) were analyzed with regard to the content of 21 detrimental and essential elements in their fruiting bodies. Two of the species (Leccinum scabrum and Leccinum versipelle) were mycorrhizal forming edible fruiting bodies while the others (Fomitopsis betulina and Inonotus obliquus) parasitic used in alternative medicine. The samples were collected near the town of Vimperk in the Bohemian Forest, the Czech Republic. L. scabrum accumulated Ag, Rb, Cd, Cs, Se, Cu, and Zn with bioconcentration factors of 22, 5.5, 4.7, 3.2, 2.0, 1.7, and 1.4, respectively. Similar trend in bioconcentration was revealed for L. versipelle with bioconcentration factors of 28, 5.2, 2.4, 1.9, 1.6, and 1.6 determined for Ag, Rb, Cu, Se, Zn, and Cd, respectively. Considerably high contents of Ca (400 ± 190 mg kg-1 dry matter), Fe (110 ± 30), Mg (1100 ± 300), and Zn (220 ± 90) were found in F. betulina. Similarly, high contents of Ca (1000 ± 700 mg kg-1 dry matter), Fe (110 ± 30), Mg (2000 ± 1100), Mn (410 ± 270), Rb (160 ± 60), and Zn (140 ± 70) were determined for I. obliquus. The different lifestyles (mycorrhizal vs. parasitic) were reflected in 13 significant differences of element contents.

The three-year monitoring of 18 elements in five edible mushroom species collected from an old orchard.

The content of Al, As, Be, Cd, Ca, Cr, Co, Cu, Fe, Pb, Li, Mg, Mn, Ni, Rb, Se, Sr, and Zn in fruiting bodies of edible mushrooms Calocybe gambosa, Entoloma clypeatum, Entoloma saepium, Xerocomellus chrysenteron, and Amanita rubescens growing in an orchard planted with fruit trees and situated close to a high-grown forest was studied during years 2016-2018. A. rubescens showed the highest potential of the element accumulation with bioconcentration factors of 48.5, 16.2, 7.80, 6.53, 1.75, and 1.68 obtained for Rb, Cd, Cu, Zn, Sr, and Mg, respectively. Both Entoloma species accumulated the elements similarly with bioconcentration factors >1.0 obtained for Rb, Cu, Cd, and Mg. Bioconcentration factors <0.05 were obtained for Al, Cr, Fe, and Pb in all studied species. The contents of beryllium (<0.1 mg/kg dry matter) were always the lowest among the studied elements. The contents of some elements of studied mushroom species significantly fluctuated over the years. Despite the fact that some studied elements (As, Be, Cd, Pb, Ni) are considerably toxic for humans, the pronounced effect on health is not expected if the studied mushroom species are consumed occasionally and do not represent the main component of the diet.

The fate of selected heavy metals and arsenic in a constructed wetland.

The fate of Cd, Pb, Cu, Zn, Ni, Cr, and As in a horizontal subsurface flow-constructed wetland was studied. The concentrations of the risk elements in treated municipal wastewater, wetland sediments, and Phragmites australis biomass were determined. Most of the studied elements were removed from the wastewater with fair efficiencies. On the other hand, As was released to treated water in the wetland bed. The removal efficiencies obtained for the individual elements were as follows: 64.2, 48.7, 70.0, 93.9, 63.6, 63.8, and -236.2%, respectively. The concentrations measured in sediments were the highest for samples taken 1 m from the inflow zone. They were 4.11, 2.01, 6.01, 4.85, 3.39, 9.30, and 3.17 times higher as compared to the samples taken in the distance of 10 m. The pollutants were preferentially deposited at the front part of the wetland bed where anaerobic conditions predominated and sulfate reduction took place. There were no significant differences in the concentrations of the studied elements in the aboveground biomass (Phragmites australis) samples taken in the distances of 1, 5, and 10 m from the inflow zone. However, the concentrations measured in the belowground biomass samples were significantly higher for samples taken at the front part of the wetland bed. The individual element concentration ratios between the below- and aboveground biomass measured for samples taken 1 m from the inflow zone were 4.97, 5.97, 2.21, 1.58, 2.26, 5.70, and 2.66 for Cd, Pb, Cu, Zn, Ni, Cr, and As, respectively.

DIMSCAN: a microcomputer fluorescence-based cytotoxicity assay for preclinical testing of combination chemotherapy.

DIMSCAN is a semiautomatic fluorescence-based digital image microscopy system that quantifies relative total (using a DNA stain) or viable (using fluorescein diacetate [FDA]) cell numbers in tissue culture multiwell plates ranging from 6 to 384 wells per plate. DIMSCAN is a rapid and efficient tool for conducting in vitro cytotoxicity assays across a 4 log dynamic range. The specificity of detecting viable cells with FDA is achieved by using digital image processing and chemical quenching of fluorescence in nonviable cells with eosin Y. Average scan time for the most commonly used format, a 96-well plate, is 6 min. Cytotoxicity for neuroblastoma cell lines measured by DIMSCAN was found to be comparable to manual Trypan blue dye exclusion counts or colony formation in soft agar, but with a significantly wider dynamic range, which enables drug combination studies used to detect synergistic or antagonistic interactions. The linearity of DIMSCAN was validated (r2 = 0.99967 +/- 0.0003) for cells stained with FDA deposited using a fluorescence-activated cell sorter, documenting a dynamic range > 4 logs, and the ability to detect a single viable cell in a well 93% of the time. DIMSCAN has been used to demonstrate preclinical activity of cytotostatic and cytotoxic drugs and drug combinations that have subsequently shown activity in clinical trials.