Skip to main content
Springer logoLink to Springer
. 2016 Aug 11;23(21):21517–21522. doi: 10.1007/s11356-016-7371-0

Bio- and toxic elements in edible wild mushrooms from two regions of potentially different environmental conditions in eastern Poland

Justyna Brzezicha-Cirocka 1, Małgorzata Mędyk 2, Jerzy Falandysz 2,, Piotr Szefer 1
PMCID: PMC5099350  PMID: 27510166

Abstract

In the present study, the composition of bio-elements (K, Na, Mg, Ca, Fe, Cu, Zn) and toxic elements (Ag, Cd) in seven edible mushrooms from the rural and woodland region of Morąg (north-eastern Poland) and the rural and industrial region of the Tarnobrzeska Upland (south-eastern Poland) were investigated using a validated method. The species examined were Boletus edulis, Cantharellus cibarius, Leccinum aurantiacum, Leccinum versipelle, Lycoperdon perlatum, Suillus luteus, and Xerocomus subtomentosus. Final determination was carried out by flame atomic absorption spectroscopy (FAAS) after microwave-assisted decomposition of sample matrices with solutions of concentrated nitric acid in the pressurized polytetrafluoroethylene vessels. The contents of the alkali elements and alkali earth elements were determined in the species surveyed. The alkali elements, earth alkali elements, and transition metals (Ag, Cu, Zn, Fe, and Mn) were at typical concentrations as was determined for the same or similar species elsewhere in Poland and Europe. The results may suggest a lack of local and regional emissions of those metallic elements from industrialization of some sites in the Tarnobrzeska Plain. Cadmium was at elevated concentrations in L. versipelle from the Tarnobrzeska Plain but the reason—pollution or geogenic source—was unknown, while it was at typical concentrations in other species.

Keywords: Foraging, Forest, Mushrooms, Boletus, Cantharellus, Leccinum, Lycoperdon

Introduction

Wild-growing saprobic and symbiotic mushrooms may accumulate in their fruiting bodies’ considerable amounts of metallic elements and metalloids due to specificities in their physiology (Aloupi et al. 2011; Frankowska et al. 2010; Kalač 2016). Mushrooms are relatively rich in mineral constituents, both edible and inedible or poisonous species which all are eaten by game animals (wild boars, stags, and others) and may end up in humans via the food chain (Brzostowski et al. 2011; Falandysz et al. 2007a, b, 2015). This is spectacularly evidenced for radiocesium (137Cs), which is radiotoxic but also for typical toxic metals such as cadmium (Cd), lead (Pb), mercury (Hg), or silver (Ag), which are well bio-concentrated from soil by many mushrooms (Borovička et al. 2010; Falandysz and Brzostowski, 2007; Malinowska et al. 2006; Solomko et al. 1986; Vinichuk et al. 2010).

Edible wild-growing mushrooms with an estimated number of 2000 species worldwide are a portion of a larger group of similar species (fungi forming fruit bodies in the form of mushrooms or similar shapes which are also called sporocarps) in the Kingdom of Fungi, and more studies are needed to characterize their mineral and other compound contents and compositions (Kalač 2016). An initial step in getting insight into mineral content and composition of edible mushrooms from the wild and their potential to accumulate minerals is the examination of crude (raw) fruiting bodies and the underneath substrate—soil or other (Falandysz et al. 2003, 2012; Garcia et al. 2009; Mleczek et al. 2013; Lu and Liang, 2014; Sarikurkcu et al. 2012).

This study investigates the occurrence of metallic elements (Ag, Ca, Cd, Cu, Fe, Mg, Na, K, and Zn) in fruiting bodies of seven species of mushrooms which are edible and can be foraged in Polish forests. Mushrooms were collected from two spatially distant forested areas in the north-east and south-east of Poland. The forested areas in the north-east are considered pristine when compared with other regions of the country. For example, the moss Pleurozium schreberi collected in 1975–1995 and 2010 from the north-east and north of Poland was significantly less affected by airborne Cd, Cr, Cu, Fe, Ni, Pb, and Zn than from other regions, while most polluted was from the south (Grodzińska et al. 1999; Kapusta et al. 2014).

Materials and methods

Fruit bodies of Boletus edulis Bull., Cantharellus cibarius Fr., Leccinum aurantiacum (Bull.) Gray, Leccinum versipelle (Fr. and Hök) Snell, Lycoperdon perlatum Pers., Suillus luteus (L.) Roussel, and Xerocomus subtomentosus L. were collected from the rural and woodland region near the town of Morąg in north-eastern Poland and from the Tarnobrzeska Plain (1411 km2) in south-eastern Poland, which is in part an industrial region with rural and forested areas (remainders of the Sandomierska Primeval forest) (Fig. 1.). In the Tarnobrzeska Plain region, the steel mill Huta Stalowa Wola is located in the town of Stalowa Wola (founded in 1938) and also the open-cast sulfur mine (also calcite, gypsum, quartz, aluminum oxide, celestine, and barite) in the Machów site (operated from 1964 to 1992) near the town of Tarnobrzeg.

Fig. 1.

Fig. 1

Location of the sampling sites: Morąg (coordinates 53° 54′ 58 57″ N 19° 55′ 40 25″ E) and Tarnobrzeska Plain (coordinates 50°35′ N 21°41′ E) in Poland (Google maps; color figure available online)

Mushrooms (from 14 to 32 fruiting bodies per species) were cleaned from plant and soil debris, placed into plastic tray of an electrically heated commercial dryer, dried at 65 °C to constant mass and further ground in porcelain mortars. The subsamples of powdered fungal materials were digested with a solution of concentrated (65 %) nitric acid (Suprapur® Merck) in pressurized vessels made of polytetrafluoroethylene (PTFE) in an automatic microwave digestion system (MLS 1200). The metallic element concentrations were determined in an air-acetylene flame with the atomic absorption spectroscopy (AAS) method, using a background correction with a deuterium lamp. In order to determine the elements K and Na, cesium (Cs) salt was added to the samples as an ionization buffer at a concentration of 0.2 % w/v, and for Ca and Mg measurements, lanthanum (La) salt was added at a concentration of 0.1 % w/v as a releasing agent (Malinowska et al. 2004). Analytical control and analytical quality (AC/AQ) of determination were achieved by examination of procedural blanks and certified standard reference materials such as fish flour (SRM), lyophilized muscle tissue (MA-B-#/TM), and sea lettuce (BCR-279 IRMM Ulva lactuca). The results obtained after examination of the reference materials were satisfactory (Table 1). The computer software Statistica version 10.0 (Statsoft Polska, Kraków, Poland) was used for statistical analysis of data.

Table 1.

Results (mg kg−1 dry biomass) of the measurements of accuracy of the analytical data using certificate reference materials CRM 279 Ulva lactuca (sea lettuce), SRM (fish flour), and MA-B-#/TM (lyophilized muscle tissue)

Element Declared value Own result RSD (%) Recovery (%)
Cda 0.274 ± 0.022 0.232 ± 0.024 10.3 84.7
Cua 13.14 ± 0.37 13.09 ± 0.23 1.65 99.6
Pba 13.48 ± 0.36 13.10 ± 0.98 7.48 97.2
Zna 51.30 ± 1.20 50.24 ± 1.59 3.16 97.9
Hgb 0.21 ± 0.02 0.26 ± 0.03 11.5 123.8
Fec 95.4 92.5 ± 3.1 3.37 97.0
Mnc 2.62 2.39 ± 0.09 3.76 91.2
Cac 3490 3456 ± 70 2.02 99.0
Mgc 1130 1040 ± 39 3.71 92.0
Nac 2160 1776 ± 53 2.97 82.2
Kc 9320 9855 ± 452 4.59 105.7

aCRM 279 Ulva lactuca (sea lettuce)

bSRM (fish flour)

cMA-B-#/TM (lyophilized muscle tissue)

Results and discussion

Bio-elements

Baseline data on concentrations of the macro- and trace metallic elements determined in the mushrooms from the Morąg and Tarnobrzeska Plain sites are given in Table 1. The median values of the alkali element concentrations ranged from 27,000 to 47,000 mg kg−1 dry biomass (db) for potassium and from 57 to 260 mg kg−1 db for sodium. Hence, mushrooms foraged from the forests nearby to Morąg and from the Tarnobrzeska Plain, like many other mycorrhizal species collected in the wild from unpolluted areas, can be considered as a component of a diet that is rich in potassium and low in sodium.

Mushrooms as foodstuff can be a good source of minerals for human nutrition. However, minerals may leach out of the flesh of cooked mushrooms, e.g., into a liquid phase, when mushrooms are boiled at a short time (blanched), and the liquid is discarded. Without a doubt, all inorganic constituents well soluble in water will highly diminish in blanched mushrooms but the same will happen to some toxic elements, e.g., radiocesium. Another question is the bioavailability of minerals from mushrooms in the alimentary tract of man, which is a little-known process. It can be anticipated that mineral constituents easily leach out during blanching of fresh/frozen or cold soaking (macerating) of dried mushrooms, e.g., alkaline elements. In the absence of blanching or soaking, minerals in mushroom meals may be well bioavailable.

B. edulis from both sites showed in whole fruiting bodies similar concentrations of potassium—median values respectively at 27,000 and 31,000 mg kg−1 db (Table 2), which is consistent with data reported for caps and stipes of this species collected from other locations in Poland (Frankowska et al. 2010). In L. perlatum, potassium was at 28,000 mg kg−1 db which was similar to B. edulis. Both C. cibarius with potassium at 47,000 mg kg−1 db and X. subtomentosus with 46,000 mg kg−1 db in caps and 44,000 mg kg−1 db in stipes in this study can be considered as richer in this element than B. edulis and L. perlatum. Those data on potassium in C. cibarius and X. subtomentosus agreed with results from other studies (Falandysz and Drewnowska, 2015; Jarzyńska et al. 2012). The mushrooms of the genus Leccinum such as L. aurantiacum and L. versipelle were rich and similar in the content of potassium, which was, respectively, at 33,000 and 36,000 mg kg−1 db (median values). Those concentrations of potassium are consistent with the content in other Leccinum spp., e.g., L. scabrum (Bull.) gray (range of medians for caps at 34,000–52,000 mg kg−1 db) and L. duriusculum (Schulzer ex Kalchbr.) singer (median at 37,000 mg kg−1 db) (Falandysz et al. 2007c; Jarzyńska and Falandysz, 2012a). Potassium content in S. luteus with a median value in caps at 34,000 mg kg−1 db and in stipes at 35,000 mg kg−1 db was consistent with the median values for S. grevillei (range 27,000–40,000 mg kg−1 db for caps and 21,000–38,000 mg kg−1 db for stipes) (Chudzyński and Falandysz 2008). In view of the results obtained for potassium and in consideration of the literature data for the same species or genus, the industrialization of the Tarnobrzeska Plain was without an impact on the potassium content of mushrooms from the wild in this location.

Table 2.

Trace elements in mushrooms from the region of Morąg (M) and Tarnobrzeska Plain (T) (mean value ± SD, median value—in parentheses—and range; mg kg−1 dry biomass)

Site Speciesa Element
K Na Mg Ca Cu Zn Fe Mn Ag Cd
M Cantharellus cibarius
(W) n = 16 (162)
49,000 ± 4600
(47,000)
42,000–59,000
240 ± 58
(260)
140–360
1200 ± 130
(1100)
980–1400
1000 ± 260
(1000)
670–1500
54 ± 12
(52)
33–77
82 ± 9
(80)
69–100
330 ± 100 (330)
170–520
30 ± 10
(27)
20–63
0.53 ± 0.16
(0.55)
0.17–0.82
0.58 ± 0.05
(0.57)
0.49–0.67
M Lycoperdon perlatum
(W) n = 16 (138)
28,000 ± 2500
(28,000)
26,000–35,000
81 ± 20
(84)
47–120
1900 ± 250
(1900)
1700–2600
170 ± 160
(120)
68–730
110 ± 23 (100)
75–150
200 ± 23
(200)
170–240
500 ± 240
(460)
280–1200
46 ± 7
(46)
36–60
2.0 ± 0.6
(2.0)
1.1–3.9
2.2 ± 0.6
(2.4)
1.5–2.9
M Boletus edulis (W)
n = 32
27,000 ± 3000
(27,000)
21,000–31,000
360 ± 380
(210)
57–1400
910 ± 160
(890)
680–1300
480 ± 170
(460)
160–900
37 ± 16
(41)
15–70
160 ± 38
(160)
71–220
200 ± 150 (150)
51–610
21 ± 10
(20)
9.0–47
1.1 ± 0.8
(0.85)
0.16–3.1
2.8 ± 2.4
(2.2)
0.36–10
T Boletus edulis (W)
n = 29
32,000 ± 5600
(31,000)
24,000–41,000
190 ± 140
(160)
18–560
850 ± 100
(860)
680–1000
200 ± 53
(190)
110–300
36 ± 18
(35)
6.0–72
210 ± 43
(130)
130–320
47 ± 44
(35)
25–210
8.6 ± 3.7 (9.2)
4.0–15
WD 5.2 ± 4.7
(2.7)
0.33–18
M Leccinum aurantiacum
(W) n = 32
35,000 ± 7500
(33,000)
22,000–49,000
230 ± 170
(170)
19–680
1100 ± 380
(1100)
340–1900
580 ± 320
(520)
110–1600
41 ± 27
(37)
11–150
112 ± 76
(100)
20–320
270 ± 260
(150)
22–1100
24 ± 17
(17)
5.4–73
0.63 ± 0.63
(0.39)
0.18–3.3
0.81 ± 0.87 (0.56)
0.18–4.9
T Lecinum versipelle
(W) n = 29
41,000 ± 41,000
(36,000)
11,000–250,000
110 ± 52
(92)
10–250
1400 ± 1500
(1100)
440–9200
250 ± 94
(220)
110–490
36 ± 21
(30)
6.7–91
170 ± 110
(190)
16–550
92 ± 100
(47)
2.5–460
9.2 ± 3.7
(9.0)
4.2–19
WD 14 ± 14
(9.8)
0.97–57
T Suillus luteus
(C)
n = 15
40,000 ± 13,000
(34,000)
23,000–75,000
100 ± 57
(84)
24–200
1300 ± 240
(1300)
970–1900
480 ± 160
(480)
320–980
20 ± 7
(17)
11–33
120 ± 30
(110)
78–180
360 ± 140
(360)
150–740
39 ± 11
(40)
24–62
WD 0.53 ± 0.19
(0.57)
0.19–0.80
T Suillus luteus
(S)
n = 14
38,000 ± 18,000
(35,000)
12,000–71,000
110 ± 66
(98)
25–220
890 ± 360
(810)
430–2000
610 ± 250
(620)
220–1100
7.9 ± 4.0
(6.3)
4.0–17
49 ± 25
(43)
18–120
280 ± 20
(310)
120–540
40 ± 18
(35)
15–76
WD 0.58 ± 0.37
(0.48)
0.23–1.7
T Xerocomus subtomentosus (C) n = 15 45,000 ± 10,000
(46,000)
11,000–53,000
54 ± 20
(57)
23–90
1200 ± 190
(1200)
610–1300
200 ± 140
(190)
47–500
24 ± 7
(25)
13–36
190 ± 47
(180)
94–300
190 ± 98
(200)
63–340
12 ± 6
(9.3)
6.7–27
WD 9.4 ± 3.6
(9.3)
3.6–16
T Xerocomus subtomentosus (S) n = 15 43,000 ± 7500
(44,000)
30,000–59,000
59 ± 22
(58)
17–100
900 ± 200
(830)
540–1300
120 ± 62
(120)
20–230
16 ± 7
(16)
7.5–30
110 ± 40
(100)
58–180
68 ± 21
(63)
42–97
10 ± 5
(8.6)
4.3–19
WD 7.5 ± 3.2
(7.1)
3.3–14

WD without data

aNumber of pooled samples and total number of fruit bodies (in parentheses); part of fruit body: W whole fruiting bodies, C caps, S stipes

Mushrooms are considered as a foodstuff very low in sodium (Vetter, 2003). In this study, the median values of sodium in a particular mushroom species or their morphological parts were below 300 mg kg−1 db, which is consistent with data reviewed recently for several species (Falandysz and Borovička, 2013).

Median values of magnesium and calcium, the alkali earth elements investigated in this study, were at a range of 810–1900 mg kg−1 db (Mg) and 120–1000 mg kg−1 db (Ca) (Table 2). They are both elements essential for biota, but mushrooms are usually substantially lower in calcium than in magnesium content (Falandysz and Borovička, 2013). The discrepancies in the median values of magnesium concentrations were negligible between the capped mushrooms, while the flesh of L. perlatum was more rich in this element and showing the maximum value mentioned earlier. Mushrooms in this study differed highly in concentrations of calcium concerning both different species but also individuals of the same species or species from the same genus as well as the morphological parts of fruit bodies (Table 2). Calcium as well as sodium, barium, and strontium occurred at greater concentrations in stipes than in caps of mature mushrooms (Falandysz and Borovička, 2013).

The transition metals such as Cu, Zn, Fe, and Mn are important cofactors in the enzymes of biota. A mushroom that is exceptionally rich in iron is Suillus variegatus (Sw.) Richon and Roze, with iron concentrations reported at a range of 3300–4100 mg kg−1 db (Falandysz et al. 2001). The range of the median values for iron in mushrooms surveyed was at 35–460 mg kg−1 db.

Mushrooms collected from the wild are usually rich in copper and zinc both of which are physiologically essential, while their concentrations differ for the species (Falandysz and Borovička, 2013). L. perlatum was richer both in Cu and Zn than other species examined, and the median values of their concentrations in caps or whole fruiting bodies were, respectively, at 100 and 16–52 mg kg−1 db for Cu, and at 200 and 80–190 mg kg−1 db for Zn. Stipes of S. luteus were much lower in Cu and Zn than caps (p < 0.05; Man-Whitney U test). Mushrooms of the genus Boletus are lower in copper than those of the genus Agaricus or Macrolepiota ((Alonso et al. 2003; Gucia et al. 2012a, b; Jorhem and Sundström, 1995; Mleczek et al. 2015). Copper in C. cibarius collected (median at 52 mg kg−1 db) and also zinc (median at 80 mg kg−1 db) were in typical concentrations for this species. For example, copper in C. cibarius from Spain was reported at 53–70 mg kg−1 db and from Sweden at 46 mg kg−1 db, while zinc, respectively, at 71–100 and at 110 mg kg−1 db (Alonso et al. 2003; Jorhem and Sundström, 1995).

S. luteus and L. perlatum showed manganese in fruiting bodies at 35–46 mg kg−1 db, and they were substantially richer in this element than other species in this study for which medians ranged from 8.6 to 27 mg kg−1 db (p < 0.05; Man-Whitney U test). Both the earth alkali elements and the transition metals (Cu, Zn, Fe, and Mn) in mushrooms were found at concentrations similar to those for the same or similar species elsewhere in Europe. The results may suggest a lack of local and regional emissions of those metallic elements from industrialization of some sites in the Tarnobrzeska Plain.

Toxic elements

The toxic cadmium and silver determined in mushrooms in this study are both chalcophile elements, while the silver (Ag+) ion is highly proteotoxic. All specimens examined showed cadmium at a detectable concentration, while X. subtomentosus, L. versipelle, and B. edulis were substantially richer in this element than other species (Table 2). C. cibarius, L. aurantiacum, and S. luteus can be considered as low in cadmium (medians <1.0 mg kg−1 db). Exceptionally high in cadmium was L. versipelle from the Tarnobrzeska Plain for which the median value in whole fruiting bodies was at 9.8 mg kg−1 db. Currently, there is a lack of credible data on cadmium in L. versipelle from other regions of Poland, and it cannot be determined whether the measured cadmium values are geogenic or largely anthropogenic. Mercury in L. versipelle from the Tarnobrzeska Plain was at a similar concentration for this element to sites considered as uncontaminated from local or regional emission sources (Falandysz, 2002; Krasińska and Falandysz, 2016).

Leccinum scabrum sampled from the background (unpolluted) areas of Poland contained cadmium in caps at 2.4 to 5.7 mg kg−1 db (medians) (Falandysz et al. 2007c). Cadmium in Leccinum griseum (Quél.) Bresinsky & Manfr. Binder from a single site sampled in Poland was at 3.3 mg kg−1 db (median) in caps and at 1.2 mg kg−1 db (median) in stipes, and in L. duriusculum, respectively, at 1.3 db and 0.45 mg kg−1 db (Jarzyńska and Falandysz, 2012a, b). In light of those data on cadmium content of mushrooms of the genus Leccinum, the concentration recorded for L. versipelle from the Tarnobrzeska Plain seemed elevated, but more results from this region are needed to assess its possible anthropogenic origin or whether other factors are involved.

Cadmium and silver were at similar concentrations in C. cibarius, L. perlatum, and L. aurantiacum but silver was less abundant in B. edulis (Table 2). Silver and cadmium are efficiently accumulated from soil and other substrata by different mushrooms but fewer data are available on silver and a possible risk from this element in edible mushrooms and other foods than for cadmium (Byrne and Tušek-Žnidarič, 1990; Falandysz and Danisiewicz, 1995; Falandysz et al., 1994).

The maximum permissible concentration for cadmium in edible mushrooms set in the European Union is 0.2 mg kg−1 fresh product for three cultivated species such as Agaricus bisporus (J. E. Lange) Imbach, (common mushroom), Pleurotus ostreatus ((Jacq.) P. Kumm. (oyster mushroom), and Lentinula edodes (Berk.) Pegler (shiitake mushroom), and for other mushrooms, it is 1.0 mg kg−1 fresh product (Commission Regulation, 2008). There is a consensus that the moisture content of fresh mushrooms is at 90 %. The cited tolerance value for cadmium in mushrooms when expressed on a dry biomass basis is 2.0 mg kg−1 for cultivated species and 10 mg kg−1 for other mushrooms. In a light of those values, only L. versipelle from the Tarnobrzeska Plain showed cadmium in whole fruiting bodies at median concentrations close to the maximum value tolerated, while in other species, cadmium was much below this value.

Conclusions

The alkali elements (K, Na), alkali earth elements (Ca, Mg), and transition metals (Ag, Cu, Zn, Fe, and Mn) in mushrooms were at concentrations similar to those determined for the same or similar species elsewhere in Poland and Europe. The results may suggest a lack of local and regional emissions of those metallic elements from industrialization of some sites in the Tarnobrzeska Plain. Cadmium was at elevated concentrations in L. versipelle from the Tarnobrzeska Plain but the reason—pollution or geogenic source—was unknown, while cadmium was at typical concentrations in other species.

Acknowledgments

Critical comment to this manuscript by Professor Roland Treu (Athabasca University) is acknowledged.

References

  1. Alonso J, García MA, Peréz-López M, Melgar JM. The concentrations and bioconcentration factors of copper and zinc in edible mushrooms. Arch Environ Contam Toxicol. 2003;44:180–188. doi: 10.1007/s00244-002-2051-0. [DOI] [PubMed] [Google Scholar]
  2. Aloupi M, Koutrotsios G, Koulousaris M, Kalogeropoulos N. Trace metal contents in wild edible mushrooms growing on serpentine and volcanic soils on the island of Lesvos, Greece. Ecotox Environ Safe. 2011;78:184–194. doi: 10.1016/j.ecoenv.2011.11.018. [DOI] [PubMed] [Google Scholar]
  3. Borovička J, Kotrba P, Gryndler M, Mihaljevič M, Řanda Z, Rohovec J, Cajthaml T, Stijve T, Dunn CE. Bioaccumulation of silver in ectomycorrhizal and saprobic macrofungi from pristine and polluted areas. Sci Total Environ. 2010;408:2733–2744. doi: 10.1016/j.scitotenv.2010.02.031. [DOI] [PubMed] [Google Scholar]
  4. Brzostowski A, Jarzyńska G, Kojta AK, Wydmańska D. Variations in metal levels accumulated in Poison Pax (Paxillus involutus) mushroom collected at one site over four years. J Environ Sci Health Part A. 2011;46:581–588. doi: 10.1080/10934529.2011.562827. [DOI] [PubMed] [Google Scholar]
  5. Byrne AR, Tušek-Žnidarič M. Studies of the uptake and binding of trace metals in fungi. Part I: accumulation and characterization of mercury and silver in the cultivated mushroom Agaricus bisporus. Appl Organomet Chem. 1990;4:43–48. doi: 10.1002/aoc.590040108. [DOI] [Google Scholar]
  6. Chudzyński K, Falandysz J. Multivariate analysis of elements content of Larch Bolete (Suillus grevillei) mushroom. Chemosphere. 2008;78:1230–1239. doi: 10.1016/j.chemosphere.2008.07.055. [DOI] [PubMed] [Google Scholar]
  7. Commission Regulation (2008) (EC) No. 629/2008 of 2 July 2008 amending Regulation (EC) No. 1881/2006 setting maximum levels for certain contaminants in foodstuffs. Official Journal of the European Union 173, 6
  8. Falandysz J. Mercury in mushrooms and soil of the Tarnobrzeska Plain, south-eastern Poland. J Environ Sci Health Part A. 2002;37:343–352. doi: 10.1081/ESE-120002833. [DOI] [PubMed] [Google Scholar]
  9. Falandysz J, Borovička J. Macro and trace mineral constituents and radionuclides in mushrooms: health benefits and risks. Appl Microbiol Biotechnol. 2013;97:477–501. doi: 10.1007/s00253-012-4552-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Falandysz J, Brzostowski A. Mercury and its bioconcentration factors in Poison Pax (Paxillus involutus) from various sites in Poland. J Environ Sci Health Part A. 2007;42:1095–1100. doi: 10.1080/10934520701418599. [DOI] [PubMed] [Google Scholar]
  11. Falandysz J, Danisiewicz D. Bioconcentration factors (BCF) of silver in wild Agaricus campestris. Bull Environ Contam Toxicol. 1995;55:122–129. doi: 10.1007/BF00212398. [DOI] [PubMed] [Google Scholar]
  12. Falandysz J, Drewnowska M. Macro and trace elements in Common Chanterelle (Cantharellus cibarius) mushroom from the European background areas in Poland: Composition, accumulation, dietary exposure and data review for species. J Environ Sci Health Part B. 2015;50:374–387. doi: 10.1080/03601234.2015.1000190. [DOI] [PubMed] [Google Scholar]
  13. Falandysz J, Bona H, Danisiewicz D. Silver content of wild-grown mushrooms from northern Poland. Zeitschr Lebensm- Unters -Forsch. 1994;199:222–224. doi: 10.1007/BF01193449. [DOI] [PubMed] [Google Scholar]
  14. Falandysz J, Szymczyk K, Ichihashi H, Bielawski L, Gucia M, Frankowska A, Yamasaki S. ICP/MS and ICP/AES elemental analysis (38 elements) of edible wild mushrooms growing in Poland. Food Addit Contam. 2001;18:503–513. doi: 10.1080/02652030119625. [DOI] [PubMed] [Google Scholar]
  15. Falandysz J, Brzostowski A, Kawano M, Kannan K, Puzyn T, Lipka K. Concentrations of mercury in wild growing higher fungi and underlying substrate near lake Wdzydze, Poland. Water Air Soil Poll. 2003;148:127–137. doi: 10.1023/A:1025422017868. [DOI] [Google Scholar]
  16. Falandysz J, Kunito T, Kubota R, Brzostowski A, Mazur A, Falandysz JJ, Tanabe S. Selected elements of Poison Pax Paxillus involutus. J Environ Sci Health Part A. 2007;42:1161–1169. doi: 10.1080/10934520701418672. [DOI] [PubMed] [Google Scholar]
  17. Falandysz J, Kunito T, Kubota R, Lipka K, Mazur A, JJ F, Tanabe S. Selected elements in Fly Agaric Amanita muscaria. J Environ Sci Health Part A. 2007;42:1615–1623. doi: 10.1080/10934520701517853. [DOI] [PubMed] [Google Scholar]
  18. Falandysz J, Kunito T, Kubota R, Bielawski L, Mazur A, Falandysz JJ, Tanabe S. Selected elements in Brown Birch Scaber Stalk Leccinum scabrum. J Environ Sci Health Part A. 2007;42:2081–2088. doi: 10.1080/10934520701626993. [DOI] [PubMed] [Google Scholar]
  19. Falandysz J, Widzicka E, Kojta AK, Jarzyńska G, Drewnowska M, Danisiewicz-Czupryńska D, Dryżałowska A, Lenz E, Nnorom IC. Mercury in Common Chanterelles mushrooms: Cantharellus spp. update. Food Chem. 2012;133:842–850. doi: 10.1016/j.foodchem.2012.01.102. [DOI] [Google Scholar]
  20. Falandysz J, Zhang J, Wang Y, Krasińska G, Kojta A, Saba M, Shen T, Li T, Liu H. Evaluation of the mercury contamination in mushrooms of genus Leccinum from two different regions of the world: accumulation, distribution and probable dietary intake. Sci Total Environ. 2015;537:470–478. doi: 10.1016/j.scitotenv.2015.07.159. [DOI] [PubMed] [Google Scholar]
  21. Frankowska A, Ziółkowska J, Bielawski L, Falandysz J. Profile and bioconcentration of minerals by King Bolete (Boletes edulis) from the Płocka Dale in Poland. Food Addit Contam B. 2010;3:1–6. doi: 10.1080/19440040903505232. [DOI] [PubMed] [Google Scholar]
  22. García MA, Alonso J, Melgar MJ. Lead in edible mushrooms levels and bioaccumulation factors. J Hazard Mater. 2009;167:777–783. doi: 10.1016/j.jhazmat.2009.01.058. [DOI] [PubMed] [Google Scholar]
  23. Grodzińska K, Szarek-Łukaszewska G, Godzik B. Survey of heavy metal deposition in Poland using mosses as indicators. Sci Total Environ. 1999;229:41–51. doi: 10.1016/S0048-9697(99)00071-6. [DOI] [Google Scholar]
  24. Gucia M, Kojta AK, Jarzyńska G, Rafał E, Roszak M, Osiej I, Falandysz J. Multivariate analysis of mineral constituents of edible Parasol Mushroom (Macrolepiota procera) and soils beneath fruiting bodies collected from northern Poland. Environ Sci Poll Res. 2012;19:416–431. doi: 10.1007/s11356-011-0574-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Gucia M, Jarzyńska G, Kojta AK. Temporal variability in twenty chemical elements content of Parasol Mushroom (Macrolepiota procera) collected from two sites over a few years. J Environ Sci Health Part B. 2012;47:81–88. doi: 10.1080/03601234.2012.611433. [DOI] [PubMed] [Google Scholar]
  26. Jarzyńska G, Falandysz J. Metallic elements profile of Slate Bolete (Leccinum duriusculum) mushroom and associated soil horizon. J Geochem Expl. 2012;121:69–75. doi: 10.1016/j.gexplo.2012.07.001. [DOI] [Google Scholar]
  27. Jarzyńska G, Falandysz J. Metallic elements profile of Hazel (Hard) Bolete (Leccinum griseum) mushroom and associated upper soil horizon. African J Biotechnol. 2012;11:4588–4594. [Google Scholar]
  28. Jarzyńska G, Chojnacka A, Dryżałowska A, Nnorom IC, Falandysz J. Concentrations and bioconcentration factors of minerals by yellow-cracking Bolete (Xerocomus subtomentosus) mushroom collected in Noteć Forest, Poland. J Food Sci. 2012;77:H202–H206. doi: 10.1111/j.1750-3841.2012.02876.x. [DOI] [PubMed] [Google Scholar]
  29. Jorhem L, Sundström B. Levels of some trace elements in edible fungi. Zeitschr Lebensm- Unters –Forsch. 1995;201:311–316. doi: 10.1007/BF01192723. [DOI] [PubMed] [Google Scholar]
  30. Kalač P. Edible mushrooms, chemical composition and nutritional value. London: Academic Press; 2016. [Google Scholar]
  31. Kapusta P, Szarek-Łukaszewska G, Godzik B. Present and past deposition of heavy metals in Poland as determined by moss monitoring. Pol J Environ Stud. 2014;23:2047–2053. doi: 10.15244/pjoes/27812. [DOI] [Google Scholar]
  32. Krasińska G, Falandysz J. Mercury in Orange Birch Bolete Leccinum versipelle and soil substratum: bio-concentration by mushroom and probable dietary intake by consumers. Environ Sci Poll Res. 2016;23:860–869. doi: 10.1007/s11356-015-5331-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Lu J-F, Liang C-Z. Risk assessment of heavy metal pollution in edible fungi in Zhejiang province. J Beijing Univ Agric. 2014;29:33–37. [Google Scholar]
  34. Malinowska E, Szefer P, Falandysz J. Metals bioaccumulation by bay bolete, Xerocomus badius, from selected sites in Poland. Food Chem. 2004;84:405–416. doi: 10.1016/S0308-8146(03)00250-4. [DOI] [Google Scholar]
  35. Malinowska E, Szefer P, Bojanowski R. Radionuclides content in Xerocomus badius and the other commercial mushrooms from several regions of Poland. Food Chem. 2006;97:19–24. doi: 10.1016/j.foodchem.2005.02.048. [DOI] [Google Scholar]
  36. Mleczek M, Magdziak Z, Goliński P, Siwulski M, Stuper-Szablewska K. Concentrations of minerals in selected edible mushroom species growing in Poland and their effect on human health. Acta Sci Pol Technol Aliment. 2013;12:203–214. [Google Scholar]
  37. Mleczek M, Siwulski M, Mikołajczak P, Gąsecka M, Rissmann I, Goliński P, Sobieralski K. Differences in Cu content in selected mushroom species growing in the same unpolluted areas in Poland. J Environ Sci Health Part B. 2015;50:659–666. doi: 10.1080/03601234.2015.982427. [DOI] [PubMed] [Google Scholar]
  38. Sarikurkcu C, Tepe B, Solak MH, Cetinkaya S. Metal concentrations of wild edible mushrooms from Turkey. Ecol Food Nutr. 2012;51:346–363. doi: 10.1080/03670244.2012.674448. [DOI] [PubMed] [Google Scholar]
  39. Solomko EF, Grodzinskaya AA, Paschenko LA, Pchelintseva RK. Mineralnij szosztav nekotorih kultivirujemih i dikorasztusih gribov klassa Basidiomycetes. (Mineral composition of some cultivated and wild fungi of the class Basidiomycetes) Mikologia i fitopatologii. 1986;20:474–478. [Google Scholar]
  40. Vetter J. Data on sodium content of common edible mushrooms. Food Chem. 2003;81:589–593. doi: 10.1016/S0308-8146(02)00501-0. [DOI] [Google Scholar]
  41. Vinichuk M, Taylor AFS, Rosén K, Johanson KJ. Accumulation of potassium, rubidium and caesium (133Cs and 137Cs) in various fractions of soils and fungi in a Swedish forest. Sci Total Environ. 2010;408:2543–2548. doi: 10.1016/j.scitotenv.2010.02.024. [DOI] [PubMed] [Google Scholar]

Articles from Environmental Science and Pollution Research International are provided here courtesy of Springer

RESOURCES