Skip to main content
Springer logoLink to Springer
. 2025 Jun 24;197(7):801. doi: 10.1007/s10661-025-14201-4

Which trace elements are accumulated in fronds of the Athyrium filix-femina fern? a study from the Czech Republic

Ivan Suchara 1, Václav Procházka 2,, Julie Sucharová 1, Marie Holá 1
PMCID: PMC12187792  PMID: 40555890

Abstract

A screening test using XRF spectroscopy was done to map element concentrations in fronds of the Athyrium filix-femina fern growing at 244 coniferous forest plots across the Czech Republic. In the next step, 45 elements in fronds of the ferns coming from selected sites with contrasting geological and climatic conditions were determined using prevalently ICP-OES and ICP-MS methods. To our knowledge, such a number of elements analyzed is unprecedented in literature data of this important fern species. Element contents of forest floor humus, topsoil and subsoil from the same sites were adopted from previously performed analyses. To estimate element uptake and accumulation by ferns, the element distribution in fern fronds was correlated with that of soil covers and with selected site-specific factors. Bioconcentration and enrichment factors referred to the element contents in forest floor humus and soil were used for estimation of fern abilities to accumulate elements in fronds. Besides accumulation of macronutrients, fern fronds moderately accumulated Ba, Cd, Hg, Mo, Mn, Ni, Zn and mainly lanthanides (REEs). Only several of the trace elements concentrated in granites (Rb, Cs, Be, Tl, U) have significant positive correlation between contents in fronds and those in mineral soil. Anthropogenic pollution was mainly relevant for Fe in the Ostrava industrial region.

Supplementary information

The online version contains supplementary material available at 10.1007/s10661-025-14201-4.

Keywords: Athyrium filix-femina, Element accumulation, Bioconcentration factors, Enrichment factors, Lanthanides (REE)

Introduction

Some of the about 12,000 fern species, frequently from the Pteridaceae family, accumulate or hyperaccumulate some trace elements, including several elements of major toxicological interest like As, in sporophytes and gametophytes (e.g. Eslava-Silva et al., 2023; Meharg, 2003; Srivastava et al., 2010; Xie et al., 2009). This is also true for several of about 180 species of the Athyrium genus (Van et al., 2006; Zhang et al., 2014). Element accumulation in fern bodies frequently increases in the following order: fronds < rhizomes < roots. Across fern fronds, petioles usually had lower element concentrations than blades (e.g. Jedynak et al., 2009; Samecka-Cymerman et al., 2011).

Athyrium filix-femina is widespread across three continents (Meusel et al., 1965), and several intraspecies taxa and cultivars have been recognized and cultivated. Athyrium filix-femina (further AFF) occurs across the whole territory of the Czech Republic except for the warmest regions of lowlands (Kaplan et al., 2018); however, there are no available data on its elemental composition there.

There are several studies on elemental composition of AFF from Poland, including the Czech-Polish border regions. Samecka-Cymerman et al. (2011) found relatively low concentrations of Cr, Al, Fe and V in AFF in the Giant Mts. Nevertheless, some authors reported accumulation of Ni (Parzych & Jonczak, 2018a, 2018b) and As (e.g., Jedynak et al., 2009). Also, the ability of AFF (similar to many other ferns) to accumulate lanthanides was documented (Grosjean et al., 2020).

The basis of our study is the determination of contents of 46 elements in fronds of AFF in the Czech territory at various geological units. The composition of green biomass of various other plants (moss, grass, spruce) from the sites sampled was evaluated by Suchara et al., (2011, 2017). These plants are valuable indicators of pollution for many elements; however, no significant accumulation of trace elements from the substrate has been found in the species investigated. Here, we concentrate on the influence of element contents in substrates (humus and two mineral soil horizons) and other selected site explanatory factors on element contents in fronds, with some emphasis on the ability of AFF to accumulate trace elements. Besides, in the “Discussion”, we summarize available literature data on the elemental composition of AFF fronds in Europe (except for studies with experimental chemical treatment) to facilitate the comparison of our large dataset (which is relatively unique for a single fern species) with data from other countries.

Material and methods

Samples

Specimens of AFF were collected at 244 forest plots of ca 50 × 50 m included in a network of the national moss biomonitoring campaigns (Suchara et al., 2017). Two middle-aged fronds, frequently with developed spore sacks, growing between the inner and outermost fronds were collected from 3 to 5 different fern plants within each sampling plot in August and September 2005. A photo of AFF clumps is included in Supplementary Materials. The leaves from each plot were joined into a composite sample. The samples were air dried, milled and sieved for particle diameters ≤ 0.25 mm. The dried leaves weighed 50–130 g, corresponding to about 300–600 g of fresh leaves (Prats et al., 2024).

Element content determination

A screening of elements heavier than Na in the powdered fern samples stored in ziplock bags was performed using a portable XRF analyser VANTA VRM (Olympus). The analytical mode “Geochemistry”, a spot diameter 10 mm, a sequence of two maximum beam energies 40 and 10 kV and automatic interpretation of spectra were used. The ziplock bags (made of polyethylene 0.05 mm thick) with samples were placed immediately at the window protecting the X-ray source and detector. The results of the XRF measurements (including other fern- and diverse plant species) will be published separately; however, the Si- and partly Fe contents obtained are utilized in this study. For more detailed elemental analyses, 35 frond specimens coming from sites of contrasting geological and climatic characteristics were selected (Table 1, Fig. 1).

Table 1.

Geographical coordinates, elevation, bedrock (with simplified classification into 5 groups—see ESM 3) and position in climatic areas and potential annual evaporation of the AFF sampling plots

Sampling plot order Latitude
°N
Altitude
°E
Elevation
m a. s. l
Bedrock* Bedrock classification Climatic zone** Potential evaporation (mm/y)**
1 50.9399 14.4360 460 Quartzose sandstone SAND MW7 550–600
2 50.8210 14.1769 410 Quartzose, argillaceous and green sandstone SAND MW7 550–600
3 50.7045 15.5760 790 Phyllite PHYL C6 500–550
4 50.6795 13.6199 770 Granite GRA C5 500–550
5 50.5688 14.3818 305 Quartzose sandstone SAND W2 600–650
6 50.5586 13.9075 570 Trachyte, altered basalt BAS W2 600–650
7 50.2787 16.3015 635 Greywacke and phyllite PHYL C6 500–550
8 50.2075 16.4717 715 Gneiss PAR C6 500–550
9 50.2206 17.3922 835 Muscovitic-chloritic and chloritic schist with phyllite PHYL MW1 550–600
10 50.1126 17.0680 855 Biotite and two-mica gneiss to augen schist PAR MW1 500–550
11 50.1053 12.8571 520 Granites and granodiorite GRA MW6 550–600
12 50.1518 14.0255 420 Sandy marlite, spiculite and claystone SAND MW11 650–700
13 50.0350 12.5249 555 Granite GRA W2 600–650
14 49.9861 14.5441 320 Greywacke PHYL MW11 650–700
15 49.9586 14.7875 485 Granite GRA MW7 600–650
16 49.9614 15.1957 365 Paragneiss PAR W2 650–700
17 49.9004 12.5784 585 Paragneiss to migmatite PAR MW3 550–600
18 49.9008 12.6253 600 Paragneiss PAR MW6 550–600
19 49.7649 16.1267 700 Paragneiss, gneiss to migmatite PAR W2 650–700
20 49.6649 18.7873 610 Sandstone and claystone in the Carpathian flysch SAND MW1 550–600
21 49.6206 17.3902 325 Clay shale, siltstone and greywacke PHYL MW7 600–650
22 49.6005 16.8391 585 Greywackes and clayey shale PHYL W2 650–700
23 49.5472 14.4917 635 Porphyry amphibole-biotite granite (durbachite) GRA MW4 550–600
24 49.4509 13.1954 535 Andesitic basalt BAS MW11 600–650
25 49.4599 16.5224 480 Two-mica paragneiss with garnets PAR MW4 550–600
26 49.4164 18.1225 565 Sandstone and claystone in the Carpathian flysch SAND C7 550–600
27 49.2755 15.8751 555 Granite to quartz syenite (durbachite) GRA MW4 550–600
28 49.1419 13.2536 925 Paragneiss PAR C6 550–600
29 49.0740 13.4929 910 Granite GRA C6 500–550
30 49.1878 14.4242 440 Paragneiss PAR MW7 550–600
31 49.0307 15.1937 685 Granite GRA MW2 550–600
32 49.0953 16.2002 275 Serpentine, peridotite BAS MW11 650–700
33 48.9429 16.0065 355 Migmatite to orthogneiss PAR MW7 650–700
34 48.7999 13.9835 880 Granite, melanocratic granite, granodiorite, migmatite GRA MW1 550–600
35 48.9003 17.5799 405 Sandstone and marlite in the Carpathian flysch SAND W2 650–700

*Adopted from ČGS (2024)

**Adopted from Tolasz et al. (2007)

C cold, MW moderately warm, W warm climatic areas

Fig. 1.

Fig. 1

Fig. 1

a Distribution of selected 35 sampling plots of AFF in a simplified geological map of the Czech Republic. b Map of Si content in fronds from all sites, determined by XRF. c Map of Fe contents determined by XRF and corrected by a simple linear function according to Fe determination by OES in 35 overlapping samples

The pulverized sample was dried (40 °C/4 h), and then, 0.25 g was weighed in a Teflon digestion vessel. After adding 6 ml HNO3 and 2 ml H2O2, the sample was subtotally digested in a CEM MARS 6 microwave digestion system (1200 W/200 °C/20 min). The humus and soil samples (0.200 g) were digested in a similar way, but a two-step procedure was used: 1. HNO3 + H2O2 + HF = 5.0: 2.0: 0.3–0.6 ml, 2. H3BO3 = 3–6 ml according to preliminarily determined Si contents.

Contents of the following elements were determined by solution analyses: Al, B, Ba, Ca, Fe, K, Mg, Mn, Na, P, S, Sr, Zn and (in soil and humus only) Si by ICP-OES (Avio 500, Perkin Elmer) and Ag, As, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, Ge, La, Li, Mo, Nd, Ni, Pb, Pr, Rb, Sb, Se, Sn, Th, Tl, U, V, W and Y by ICP-MS (NexION 2000, Perkin Elmer). Total Hg and C and N contents were measured directly in powdered samples using a single-purpose mercury AMA 256 atomic absorption spectrometer and a carbon and nitrogen determinator (LECO CN 928), respectively.

All measurements were performed in three independent replications (see ESM 1 for complete data). Blind samples and reference materials (IAEA Lichen 336, NIST Pine Needles 1575a, NIST Apple Leaves and LECO ALPHALPHA 502–237) were analyzed in parallel (see ESM 2 for results of reference materials analyses). No recalibration of analytical instruments had to be done.

Explanatory factors

The analytical results were related to the selected sampling plots specific characteristics, such as elevation, bedrock types and potential annual evaporation. More explanatory factors, namely pH values and element contents of humus, topsoil and subsoil of the sampling sites, were adopted from the previous measurements (Suchara et al., 2011).

Indices of element accumulation

To estimate the efficiency of AFF to accumulate elements in fronds, the bioconcentration factor (BcF) was used (e.g. Burnison, 1998):

BcF=cEf/cEs 1

where cEf and cEs represent the content of E element in frond and in soil, respectively.

Enrichment factors (EFs) (Barbieri, 2016) were computed as ratios of normalized element content in AFF to normalized element content in humus (Oh), topsoil and subsoil, respectively, using Al for chemical normalization:

(EF)=(E/Al)frond/(E/Al)substrate 2

Not enriched, slightly, moderately, severely, highly severely and extremely enriched classes were defined by the respective intervals < 1.5, [1.5;2], [2;5], [5;20], [20;40] and ≥ 40.

Cerium anomalies calculation

Cerium anomalies (Ce/Ce*) were calculated using geometric extrapolation to obtain the theoretical Ce* value (i.e. Ce concentration in case of no anomaly) by the following formula:

Ce/Ce=CeN/[PrN2/NdN] 3

where CeN, PrN and NdN are element values, normalized to the element contents in Post-Archean Australian Shales (see Barrat et al., 2023 for details). Values of Ce/Ce* significantly lower and greater than 1 mean a negative and a positive anomaly, respectively.

Statistics

Basic statistics and statistical tests and analyses were obtained in the StatSoft STATISTICA 14.0 software. Measured variables having a typically log-normal distribution were log transformed (log10 median) for statistical evaluations. Due to remaining differences from normal distribution in some transformed data, Spearman’s correlation coefficients were computed in all correlation analyses used. For cluster analysis in STATISTICA, the following parameters were used: raw variable or cases data (for Figs. 2 and 3, respectively), Ward’s method and 1–Pearson r for cluster, amalgamation rule and distance measure, respectively.

Fig. 2.

Fig. 2

Cluster analysis (Ward’s method, 1-Pearson r, Distance Linkage) dendrogram for the medians of element contents in AFF at 35 sampling sites. Medians used were log10 transformed

Fig. 3.

Fig. 3

Cluster analysis (Ward’s method, 1-Pearson r, Distance Linkage) dendrogram for 35 sampling sites of AFF with the given medians of element contents. Medians used were log10 transformed

Results

The element contents and their basic statistics for the AFF fronds specimens are presented in Table 2.

Table 2.

Basic statistics for the element contents in the AFF fronds (mg/kg), n = 35, SD standard deviation, RSD relative standard deviation, I.Q. first quartile, III.Q. third quartile, MAD median absolute deviation

Element Min Max Mean SD RSD (%) I.Q Median III.Q MAD
C 428,968 465,741 449,293 8952 2 445,000 449,229 454,000 5064
N 20,223 36,254 25,926 3643 14 23,050 25,889 28,100 2615
Ag 0.008 0.103 0.017 0.016 91 0.011 0.014 0.018 0.004
Al 50.4 260 138 56.1 40 96.7 129 170 40.4
As 0.024 0.242 0.084 0.047 54 0.050 0.072 0.100 0.024
B 16.3 77.0 27.8 9.78 35 23.2 25.4 30.9 2.67
Ba 53.1 306 136 59.0 43 94.1 127 168 38.7
Be 0.004 0.302 0.043 0.064 147 0.012 0.018 0.049 0.010
Bi 0.001 0.025 0.004 0.004 95 0.002 0.003 0.006 0.001
Ca 4260 10,763 6730 1701 25 5398 6248 8044 986
Cd 0.044 1.63 0.339 0.319 93 0.132 0.581 0.411 0.159
Ce 1.53 48.9 21.6 10.6 49 14.2 19.1 28.8 5.85
Co 0.036 0.833 0.171 0.153 90 0.082 0.114 0.222 0.045
Cr 0.307 1.85 0.489 0.261 53 0.375 0.421 0.509 0.075
Cs 0.016 20.0 1.88 3.68 193 0.179 0.415 2.47 0.319
Cu 5.04 15.3 9.24 2.22 23 7.92 9.02 10.0 1.12
Fe 72.0 300 127 44.3 34 102 112 142 14.8
Ga 0.084 0.421 0.225 0.083 36 0.167 0.208 0.251 0.043
Ge 0.086 0.488 0.220 0.091 41 0.162 0.208 0.243 0.041
Hg 0.021 0.110 0.045 0.025 54 0.027 0.036 0.054 0.010
K 14,455 32,592 23,264 4723 20 19,827 23,762 27,044 3390
La 1.62 72.4 18.4 13.0 70 11.6 15.6 20.8 4.58
Li 0.077 7.25 0.899 1.62 167 0.153 0.425 0.652 0.271
Mg 2023 6516 3318 1011 31 2752 3010 3804 425
Mn 34.1 931 146 157 112 88.35 104 142.0 22.8
Mo 0.098 1.65 0.388 0.356 96 0.166 0.234 0.443 0.104
Na 5.28 266 46.7 60.4 136 12.40 21.0 52.70 11.1
Nd 1.75 35.4 10.9 7.64 62 6.56 8.22 12.65 2.43
Ni 0.744 26.9 5.32 7.40 132 1.61 2.63 5.56 1.42
P 1102 3740 2012 643 31 1518 1913 2318 406
Pb 0.171 2.78 0.684 0.599 72 0.312 0.415 0.733 0.165
Pr 0.388 8.51 3.00 1.87 58 1.97 2.46 3.35 0.581
Rb 7.54 517 138 138 104 49.10 78.0 200 31.9
S 1339 2528 1832 264 15 1655 1852 1978 159
Sb 0.009 0.062 0.023 0.013 46 0.015 0.019 0.029 0.006
Se 0.34 0.498 0.190 0.115 58 0.104 0.159 0.249 0.061
Sn 0.029 0.122 0.056 0.024 38 0.041 0.046 0.068 0.010
Sr 9.67 64.2 28.7 14.3 50 16.70 25.4 34.15 9.18
Th 0.003 0.039 0.086 0.107 51 0.009 0.044 0.024 0.026
Tl 0.004 0.588 0.017 0.009 130 0.026 0.015 0.124 0.007
U 0.002 0.681 0.032 0.115 383 0.005 0.007 0.014 0.004
V 0.190 1.67 0.572 0.356 64 0.368 0.427 0.559 0.104
W 0.003 0.027 0.011 0.006 54 0.008 0.010 0.013 0.002
Y 0.207 35.1 3.23 5.95 70 0.988 1.57 2.975 0.953
Zn 19.7 56.7 28.0 8.10 30 23.15 26.4 28.95 3.27
Si 2973 13,344 8386 2623 31 6312 8749 10,116 2022

Results of cluster analysis for the elements in 35 fern samples and for the 35 selected sampling sites are shown in Figs. 2 and 3.

Correlation coefficients for element contents in AFF with element contents in the substrates and the explanation factors are gathered in ESM 4. Bioconcentration factors for the element contents in AFF related to the element contents in humus, the topsoil and subsoil are shown in ESM 5 and enrichment factors in ESM 6.

Macroelements

Of elements analyzed, macroelements include C, N, P, K, Ca, Mg, S, Fe and Si. They play structural, nutritional and protective roles in plant bodies. Contents of C (median 449.2 ± 5.06 g/kg) showed extremely low variability (CV 1.1%), and the sampling site factors did not significantly affect C content in AAF fronds. All significant correlations between the content of C and of other elements are negative (except for the positive correlation with Cr).

Nitrogen contents (20.2–36.3 g/kg) significantly positively correlated with P, S and Cu contents and negatively with Ba in fronds. The C:N ratios ranged from 11.9 to 22.6 and N:P ratios from 5.4 to 21.6.

Contents of P in fronds showed a wide range (1.10–3.74 g/kg). Fronds from sites with granitic bedrocks had significantly higher P concentrations and lower C:P and N:P ratios.

The relatively high contents of K in fronds (14.4–32.6 g/kg) are consistent with other studies (Tables 2 and 3). The K contents positively and negatively correlated with granitic and phyllitic bedrocks, respectively. Potassium negatively correlated with Ca and Mg in fronds and with humus pH.

Table 3.

Published data of element contents and bioconcentration factors in AFF fronds (mg/kg, unless stated otherwise) determined in European natural or seminatural biotopes

Element Range Mean (median) BcF Habitats Decomposition + analytical methods Source
Al 10–200* 110 0.01–0.02*+ Alder forest riverbank marsh, N Poland HNO3+H2O2,MP-AES Parzych & Jonczak, 2018b
103–484 354 0.04m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, ETAAS Samecka-Cymerman et al., 2011
As 2.2–2.8 n.d. Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
20* 0.01*m Soil in Ag-As mining area, S Poland HNO3, GFAAS Jedynak et al., 2009
C (%) 42 Peat birch forest, Baltic shore, N Poland K2Cr2O7, titration Mohr's Parzych, 2010
Ca 3350 Wet spruce forest, NE Poland burn, FAES Czerwiński & Pracz, 1995
1000–7000* 4000* 0.38–0.52*+ Alder forest riverbank marsh, N Poland HNO3+H2O2, FAAS Parzych & Jonczak, 2018b
4907–6879 100–220* Headwater riparian alder forest, N Poland HNO3+H2O2, FAAS Parzych & Astel, 2018
5464–9900 7232 10+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, FAAS Samecka-Cymerman et al., 2011
1120–6300* 2140* Polluted and unpolluted sites in Norway and Lithuania n.s., AAS Stapulionytė et al., 2018
3400–11100 Coniferous forests on soddy podzols, Moscow region n.s. Vtorova & Solntseva 1983
Cd 0.11–1.25 0.139 Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
0.061–0.387 (0.087) 0.13m Eastern Giant Mts., S Poland HNO3+H2O2, GFAAS Krawczyk et al., 2006
0.10–0.91 0.38 (0.35) 0.9+m Forest soils, mining and smelting area, NE Slovakia Aqua Regia, GFAAS Musilova et al., 2016
0.27 0.55•m Beech woods on acid and damp soils, Germany GFAAS/ICP-OES Neite et al., 1991
0.01–0.10 0.06 Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, ETAAS Samecka-Cymerman et al., 2011
0.013–1.30* 0.08* Polluted and unpolluted sites in Norway and Lithuania n.s., AAS Stapulionytė et al., 2018
Co 0.004–0.144 0.065 (0.074) 0.08+m Eastern Giant Mts., S Poland HNO3+H2O2, GFAAS Krawczyk et al., 2006
0.1–0.6 0.3 0.04+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, ETAAS Samecka-Cymerman et al., 2011
Cr 14.6–44.7 n.d.–0.01 Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
7.39–11.8 8.95 (8.62) 3.0+m Eastern Giant Mts., S Poland HNO3+H2O2, GFAAS Krawczyk et al., 2006
0.1–0.4 0.2 0.01+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, ETAAS Samecka-Cymerman et al., 2011
Cu 6.2–18.2 0.31–0.36 Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
9.15–11.9 10.7 (10.9) 0.94m Eastern Giant e Mts., S Poland HNO3+H2O2, FAAS Krawczyk et al., 2006
3.34–85.7 10.3 (7.61) 0.09+m Forest soils, mining and smelting area, NE Slovakia Aqua Regia, FAAS Musilova et al., 2016
19 24m Beech woods on acid and damp soils, Germany GFAAS/ICP-OES Neite et al., 1991
n.d.–29* 12.5* 1.2–1.7*+ Alder forest riverbank marsh, N Poland HNO3+H2O2, FAAS Parzych & Jonczak, 2018b
7.2–16* 9.7* 0.4*+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, ETAAS Samecka-Cymerman et al., 2011
1.4–18* 6.3* Polluted and unpolluted sites in Norway and Lithuania n.s., AAS Stapulionytė et al., 2018
Fe 130–198 n.d.–0.01 Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
41–255 116 (109) 0.03+m Eastern Giant Mts., S Poland HNO3+H2O2, FAAS Krawczyk et al., 2006
90–310* 200* 0.02–0.03*+ Alder forest river bank marsh, N Poland HNO3+H2O2, FAAS Parzych & Jonczak, 2018b
99–415 216 0.01+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, FAAS Samecka-Cymerman et al., 2011
22–1070* 115* Polluted and unpolluted sites in Norway and Lithuania n.s., AAS Stapulionytė et al., 2018
Hg n.d.–6.59 0.22 (0.05) n.d.–1.23 Forest soils, polluted by Cu and Hg smelters, NE Slovakia AAS Árvay et al., 2017
0.02–12.8 0.99 (0.06) 0.03m Forest soils, mining and Cu and Hg smelters, NE Slovakia Hg-AAS (AMA-254) Musilova et al., 2016
K (%) 0.757 Wet spruce forest, NE Poland ashing, FAES Czerwiński & Pracz, 1995
2.1–3.2* 2.63* 14.7–39.7*+ Alder forest riverbank marsh, N Poland HNO3+H2O2, FAAS Parzych & Jonczak, 2018b
1.69–2.19 4760–20335*w Headwater riparian alder forest, N Poland HNO3+H2O2, FAAS Parzych & Astel, 2018
1.44–2.86 2.02 37+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, FAAS Samecka-Cymerman et al., 2011
1.23–2.51* 1.48* Polluted and unpolluted sites in Norway and Lithuania n-a., AAS Stapulionytė et al., 2018
3.83–5.02 Coniferous forests on soddy podzols, Moscow region n.s. Vtorova & Solntseva, 1983
Mg 5180 Wet spruce forest, NE Poland FAAS Czerwiński & Pracz, 1995
2500–4600* 3500* 1.7–3.9*+ Alder forest riverbank marsh, N Poland HNO3+H2O2, FAAS Parzych & Jonczak, 2018b
3781–4068 590–3270*w Headwater riparian alder forest, N Poland HNO3+HClO4, FAA Parzych & Astel, 2018
2172–5137 3994 1.6+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, FAAS Samecka-Cymerman et al., 2011
1230–10000* 1900* 0.63+m Polluted and unpolluted sites in Norway and Lithuania n.s., AAS Stapulionytė et al., 2018
2800–6700 Spruce and pine forest on soddy podzols, Moscow region n.s. Vtorova & Solntseva, 1983
Mn 53–141 101 (107) 1.0+m Eastern Giant Mts., S Poland HNO3+H2O2, FAAS Krawczyk et al., 2006
45–130* 86.5* 0.25–0.35*+ Alder forest riverbank marsh, N Poland HNO3+H2O2, FAAS Parzych & Jonczak, 2018b
194–519 339 Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, FAAS Samecka-Cymerman et al., 2011
10–500* 45* Polluted and unpolluted sites in Norway and Lithuania n.s., AAS Stapulionytė et al., 2018
N (%) 2.380 Wet spruce forest, NE Poland Kjeldahl Czerwiński & Pracz. 1995
1.711 1.7m Peat birch forest, Baltic shore, N Poland Kjeldahl Parzych, 2010
1.06–1.83* 1.413* Headwater riparian alder forest, N Poland Kjeldahl Parzych & Jonczak, 2018a
1.00–2.36* 1.676* 1.5–1.8*+ Alder forest riverbank marsh, N Poland Kjeldahl Parzych & Jonczak, 2018b
1.40–1.41 1.62–5.42*w Headwater riparian alder forest, N Poland Kjeldahl Parzych & Astel, 2018
2.69–2.94 Coniferous forests on soddy podzols, Moscow region n.s. Vtorova & Solntseva, 1983
Na 650 Wet spruce forest, NE Poland ashing, FAES Czerwiński & Pracz, 1995
4–500* 40* Polluted and unpolluted sites in Norway and Lithuania n.s., AAS Stapulionytė et al., 2018
500–700 Coniferous forests on soddy podzols, Moscow region n.s. Vtorova & Solntseva, 1983
Ni 25.8–33.9 0.06–0.15 Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
4.49–8.54 6.65 (6.65) 2.8+m Eastern Giant Mts., S Poland HNO3+H2O2, GFAAS Krawczyk et al., 2006
13–42* 26* 2.8–3.9*+ Alder forest riverbank marsh, N Poland HNO3+H2O2, FAAS Parzych & Jonczak 2018b
1.1–4.9 2.4 0.18+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, ETAAS Samecka-Cymerman et al., 2011
P 468–2379 Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
1720 Wet spruce forest, NE Poland Spectrophotometry Czerwiński & Pracz, 1995
4000 Boreal forests n.s. Gerloff et. al., 1964 ex Larsen, 1982
1410 1.3m Peat birch forest, Baltic shore, N Poland Spectrophotometry Parzych, 2010
1500–3450* 2485* 0.36–0,40*+ Alder forest riverbank marsh, N Poland Spectrophotometry Parzych & Jonczak, 2018b
2177–2266 5385–29230*w Headwater riparian alder forest, N Poland Spectrophotometry Parzych & Astel, 2018
108–1367 858 2.9+m Forests in the Kaczawskie Mts., SW Poland Spectrophotometry Samecka-Cymerman et al., 2011
3400–4600 Coniferous forests on soddy podzols, Moscow region n.s. Vtorova & Solntseva, 1983
Pb 0.90–1.34 n.d.–0.03 Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
2.84–13.1 5.34 (4.45) 0.05+m Eastern Giant Mts., S Poland HNO3+H2O2, GFAAS Krawczyk et al., 2006
0.09–12.3 2.21 (1.10) 0.04 +m Forest soils, mining and smelting area, NE Slovakia Aqua Regia, GFAAS Musilova et al., 2016
24 0.6•m Beech woods on acid and damp soils, Germany GFAAS/ICP-OES Neite et al., 1991
2.6–9.2 5.3 0.14+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, ETAAS Samecka-Cymerman et al., 2011
0.07–99* 0.08* Polluted and unpolluted sites in Norway and Lithuania GFAAS/ICP-OES Stapulionytė et al., 2018
HNO3+HClO4, ETAAS
S 700–1400 1230 Wet pine forest, NE Poland n.s. Czerwiński & Pracz, 1995
Coniferous forests on soddy podzols, Moscow region n.s. Vtorova & Solntseva, 1983
Si (%) 0.63–1.25 Coniferous forests on soddy podzols, Moscow region n.s. Vtorova & Solntseva, 1983
Sr 29–61* 44* 0.76–0.99*+ Alder forest riverbank marsh, N Poland HNO3+H2O2,MP-AES Parzych & Jonczak, 2018b
V 0.2–2.4 0.9 0.04+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, ETAAS Samecka-Cymerman et al., 2011
Zn 14.6–44.7 0.32–0.58 Metalliferous soils, N Italy HNO3, ICP-OES Cornara et al., 2007
21.7–50.5 30.1 (26.5) 0.76+m Eastern Giant Mts., S Poland HNO3+H2O2, FAAS Krawczyk et al., 2006
12.4–73.7 39.5 (38.3) 0.21+m Forest soils, mining and smelting area, NE Slovakia Aqua Regia, FAAS Musilova et al., 2016
71 3.4•m Beech woods on acid and damp soils, Germany GFAAS/ICP-OES Neite et al., 1991
12–32* 22.5* 0.36–0.55*+ Alder forest riverbank marsh, N Poland HNO3+H2O2, FAAS Parzych & Jonczak, 2018b
40–91 61 1.0+m Forests in the Kaczawskie Mts., SW Poland HNO3+HClO4, FAAS Samecka-Cymerman et al., 2011
10–102* 15* Polluted and unpolluted sites in Norway and Lithuania n.s., AAS Stapulionytė et al., 2018

*Estimated from published diagrams, + values related to subtotal element contents, w BcF related to the element contents in surface water, * BcF related to the extractable (NH4Cl) element contents in soil, m mean value, n.a. not available

The fronds had twofold higher contents of Ca than Mg, which is generally consistent with the literature. Although both sites with peak Mg contents in fronds (6.5 and 5.95 g/kg) have Mg-rich rock substrates (serpentinite and basalt, respectively), there is no statistically significant correlation of Mg or Ca with their contents in soil. Frond Ca content correlates positively with humus pH.

Sulphur content in fronds (1.3–2.5 g/kg) correlated positively (besides N) with Na, Zn and Cu and with phyllitic bedrocks. Interestingly, there is no correlation of S in fronds and in humus, but a strong negative correlation of S in fronds and in the upper mineral horizon B1 (in deeper mineral horizon B2, S was not analyzed).

Iron content in fronds is, on average, similar to that of Mn, and it is positively correlated with Ca, Mg, Si and many trace elements like Cr. A map of Fe contents obtained by XRF is shown in Fig. 1c, where a regional enrichment in the very east (near Ostrava) is documented.

The XRF measurements showed relatively high median Si contents in AFF fronds: 8.12 ± 1.85 and 8.75 ± 1.56 g/kg from the whole country (n = 244) and from the studied plots (n = 35), respectively. Contents of Si showed a strong positive correlation with Ca, Fe, Al and many trace elements. The spatial distribution of Si contents is shown in Fig. 1b.

Microelements

Concentrations of B, Cu and Zn in fronds showed the lowest variability among the trace elements, indicating a physiological control to maintain optimal content, while the highest variability of U, Cs, Li, Tl, Be, Ni and even Na may imply low AFF control on uptake and accumulation of these elements. Average content of Mn is strongly influenced by an outlying peak value 931 mg/kg, while the range of other samples is 34–381 mg/kg.

Increased content of some microelements was associated with certain bedrock types, namely granites and durbachite (Be, Rb, Cs, Tl), sandstones (Zn) and phyllites (Pb, W; influence of the sulfidic mineralization associated with gold deposits near site 9 is possible). The site 32 with chemically contrasting serpentinite bedrock also has a high content of Cr, Ni and Cu in fronds, but the whole group of basic and ultrabasic rocks is not distinct.

Positive correlations prevail among microelement contents in fronds. Very strong mutual positive correlations showed REEs and Y, which also positively correlated with Ga, Ge, Al and Si. Contents of Cs, Rb, Sr and Tl in fronds correlated positively, and Cr, Cu, Li and Ni correlated negatively with altitude. Potential evaporation, negatively correlating with elevation (r = –0.65**), positively affected Co, Li and Th contents and negatively affected Bi, Ca, Tl and Rb contents.

Cerium anomalies

The fronds prevalently showed negative cerium anomalies with Ce/Ce* ratios 0.33–1.38, mean 0.85, SD 0.26, median 0.84 and MAD 0.21. The only three fern samples with significant positive Ce anomalies are those with the highest Mn concentrations.

Bioconcentration factors

The BcF values (see ESM 5 for complete data) mostly decreased when related to the element contents in the following order: humus > topsoil > subsoil; however, frequently, the highest BcF values were found when related to the topsoil (ESM 5). The average BcF > 1 showed some macroelements (Ca, K and Mg) and microelements (Ba, Rb, Ce, La, Nd, Pr and Y) when BcF was related to the humus element contents, while when compared with element contents in the lower mineral soil, the BcF exceeded 1 for K, Mg, Cd, Cu, Hg, Mn, Rb and Zn. Despite relatively high BcFs for Rb, the K/Rb ratios in fronds were generally higher than in humus and soil. Probably, a high BcF for B would have also been indicated; however, B content was not determined in substrates. On the other hand, Na, As, Bi, Pb, Sb, Sn, Th, Tl and W showed medians BcFs < 0.1 related to all soil layers, indicating that these elements are excluded by AFF. BcFs were relatively significantly influenced by site factors (see “Discussion” and ESM 7).

Enrichment factors

Normalized element contents in the subsoil, topsoil and humus were used as local background values for computing enrichment factors of elements in fronds. Due to relatively low Al content and enrichment in Cd, Hg, Bi, Cu, Mo, Pb, Sb and Sn (partly due to atmospheric deposition) in humus, the EFs medians except for REE and alkali elements are higher when related to element contents in soil (mainly in the subsoil) than to that in humus. Elements with no to slight enrichment in fronds were Ag, As, Bi, Cr, Fe, Li, Na, Sb, Sn, Th, U, V and W, mainly if related to the humus element contents. The highest median EFs characterize macronutrients and their analogues (Ba, Ca, Cs, K, Mg, Rb, S, Sr), some micronutrients and toxic elements (Cd, Cu, Hg, Mn, Mo, Zn) and especially REE (La, Ce, Pr, Nd) and Y.

Discussion

Cluster analysis

Figure 2 shows clusters of elements, whose variability in AFF is similar partly due to their generally similar chemical properties and common occurrence (e.g. lanthanides, or Rb and Cs). Biogenic elements tend to concentrate in the left cluster. Figure 3 shows clusters of sampling sites with most similar medians of element contents in AFF. The left cluster (13 sites) contains almost all (8 of 9) sampling sites with granitic bedrock. However, other bedrock groups are little distinct, most likely due to their internal variability and the importance of the remaining explaining variables, such as the elevation, potential evaporation or climate (Table 1).

Macroelements

Regarding carbon, the only relevant publication found (Parzych, 2010) stated a lower average C content in fronds of AFF (420 g/kg) growing in wet soils of coniferous forests in comparison to our data from drier forest soils (Table 3). The negative correlations between concentrations of C and of many other elements are due to a dilution of element pools during the growth of the frond biomass.

Nitrogen contents significantly positively correlated with other nutrients—P and S. The C:N ratios (11.9–22.6) were not significantly affected by the site elevation, potential evaporation and soil pH. Literature data (Table 3) are at disposal mainly from Poland, where mostly lower N content has been reported (associated with higher C:N ratios, e.g. about 24.5 in the fronds of AFF from muddy habitats studied by Parzych, 2010).

Contents of P in fronds showed greater variability than N and a wider range than in the most of literature data (Table 3). Fronds from sites with granitic bedrocks had significantly higher P concentrations and lower C:P and N:P ratios due to commonly increased P content in granites. The N:P ratios reflect an instantaneous fern nutritional status and local element uptake limitations (Güsewell, 2004; Koerselman & Meuleman, 1996). The N and P limitations for AFF growth were indicated for 17 and 9 sampling plots, respectively.

The positive correlation of K in fronds with granitic bedrock rather reflects the content of K-feldspar than the total K in the rocks, because liberation of K from some minerals like the white mica can be very slow. Negative correlation with Ca and Mg in fronds and with humus pH may also reflect the influence of bedrocks.

While in our data, fronds from only one site had higher content of Mg than Ca, Czerwiński and Pracz (1995) found higher content of Mg than Ca (5.18 vs. 3.34 g/kg) in fronds of AFF growing in peat soil (i.e. in a probably Mg-poor environment).

Sulphur content in fronds was higher than in the two studies from literature available (Table 3).

Iron contents in fronds are comparable to literature data. Iron is the only element documented to be regionally enriched in the major eastern industrial region between the city Ostrava and the Polish and Slovak borders (see also Fig. 1c). In contrast, the strong pollution in the northwestern region (part of the “Black triangle”) which peaked in the 1980 s has already not unequivocally influenced the distribution of any of the elements analyzed in ferns at the time of collection (2005), although it was still slightly visible in the distribution of elements in moss (Suchara et al., 2017). Similarly, the role of industrial pollution on Fe content in AFF was documented in comparison of various regions in Lithuania and Norway (Stapulionytė et al., 2018).

Contents of Si, playing structural and protective roles in plants, showed a strong positive correlation with humus pH and with many elements in fronds, e.g. Ca, some of which (e.g. Al, Ga, Th, lanthanides, partly Fe) are typical for mineral dust (as also manifested in their spatial distribution in moss—see Suchara et al., 2011, 2017). However, if we consider Al as the representative of mineral (wind-transported) dust, the ratios of other elements to Al can be used to estimate the maximum dust content (see also enrichment factors calculated from ratios of other elements to Al in ESM 6). It follows that the dust may only little contribute to the pools of elements like Si or REEs in the fronds. The Si content in fronds is low mainly on the most quartz-rich sandstones in the northern part of the Bohemian Cretaceous Basin. This can be explained by the fact that Si is mainly liberated by weathering of silicates (like feldspars) and only insignificantly from quartz.

Microelements

Obtained contents of microelements in fronds (Table 2) are comparable with available published data. Some microelements (e.g. B, Cu, Mn, Mo and Zn) in low concentrations serve as essential micronutrients while in higher concentrations they are toxic.

Concentrations of B, Cu and Zn in fronds showed the lowest variability among the trace elements, indicating a physiological control to maintain optimal content, in contrast to highly variable Cs, Li, Th and Be. The most contrasting bedrock type influencing directly trace elements in biomass is granitic rocks (Rb, Cs, Be, Tl, U). Some other rocks may be chemically very contrasting as well (e.g. quartz-rich sandstones, ultrabasic rocks), but the group of sandstones is probably highly heterogeneous (e.g. some of them can be relatively Ca-rich, or intercalated with other sediments), and basic and carbonate substrates are relatively rare in Czech coniferous forests. The trace elements concentrated in granites (Rb, Cs, Be, Tl, U) are the only elements with significant correlation between contents in fronds and those in mineral soil. In literature, an example of bedrock-dominated variability of some elements in AFF fronds was presented by Samecka-Cymerman et al. (2011) from the Giant Mts.

The peak uranium content in fronds at the site 18 (where U is also high in humus but not in mineral soil) in a former U mining area may reflect a contamination by U-enriched dust. Some role of atmospheric deposition and/or historic pollution can be also expected (in addition to gas-forming elements—N, S, Se) for elements whose contents in fronds are significantly correlated to those in humus: Mn, Sb, Sn and Zn. On the other hand, Se in fronds correlates negatively with Se in humus, and S and Zn in fronds correlate negatively with S and Zn, respectively, in mineral soil. This could indicate significant mobility of these elements in the plant-soil system.

Positive correlations like Fe–Ni and Cd-Cu–Zn in fronds may reflect associations of these elements in minerals in both bedrock and soil. Some positive correlations of elements in fronds (e.g. Hg with Al or Fe) which are missing in humus and soil could be explained by other factors, like pH. Significant negative correlations were found seldom (except for those of other elements, e.g. Ba, Cr, Ga, Se, Si and W with C), e.g. Fe-Rb, Na-Pb, K-Pb, K-Hg and Mn-Cd. Negative (with borderline statistical significance, however) correlation of both Ba and Pb with P in fronds may be caused by their decreased bioavailability in phosphorus-rich soils, as documented for Pb (Miretzky & Fernandez-Cirelli, 2008). Humus pH correlates positively with B, Ca, Ce, Ge, Hg, Mg, Th and Si and negatively with Cd, K and Rb. Contents of Rb, Si and Th in fronds correlated positively, and Li and Ni correlated negatively with elevation. Potential evaporation, negatively correlating with elevation (r = –0.70; p < 10−3), positively affected Co, Li, Na and Th contents and negatively affected Bi, Cs, Rb and Tl contents.

However, some significant correlations may be accidental due to the coincidence of many factors (e.g. elevation correlates negatively with evaporation and positively with granitic rocks).

Cerium anomalies

The prevalently negative cerium anomalies and the fact that only the three Mn-richest fern samples have significant positive Ce anomalies imply that the fern prevalently takes up REE from solutions. Soil solutions (similar to surface water) tend to be depleted in Ce3+ due to its oxidation to little soluble Ce4+ which can be bound to Fe- and Mn oxides and hydroxides (Bau & Koschinsky, 2009). No significant relationships of Ce anomalies to the site factors were found.

Bioconcentration factors

In contrast to element contents alone, the bioconcentration factors were frequently significantly influenced by site factors (see also ESM 7). For example, humus pH significantly negatively affected BcF for Ba, Be, Ca, Cd, Co, Cs, K, Mg, Mn, Na, Rb, Sr and Zn, while the elevation showed mainly positive effects on BcF, significantly for Ca, Cs, La, Nd, Pr, Rb, Si, Sr, Tl and Y. Some significant correlations of BcF related to the element contents in humus were found for bedrock types, e.g. negative correlations with sandstones (Cd, Cs, Cu, Ga, Ge and Tl), and positive with granites (Cs, Rb, Tl and U).

The site factors, except for humus pH, influence the BcFs related to mineral soil more (but partly differently) than BcFs related to humus. This is consistent with the assumption that AFF uptakes elements mainly from deeper horizon than humus. Note that in case of two sandstone sites (Nos. 2 and 5), high BcFs simply reflect extremely low contents of most elements in the mineral soil. However, such an explanation cannot be applied to elevated BcFs for elements concentrated in granites at sites with granitic bedrock.

Published BcFs determined in several studies (except for values related to water or mud in wetlands) (Table 3) did not show hyperaccumulation of any element by AFF. BcFs slightly exceeding the value 1.00 for (potentially) toxic elements Cr, Cu, Mn, Ni and Zn were reported seldom. Accumulation of these elements in AFF is explained by the effects of some bedrock types and frequently by increased atmospheric deposition rates of heavy metals at sites affected by industrial emissions (Krawczyk et al., 2006). Our study has not confirmed considerable accumulation of heavy metals in AFF in the country.

Enrichment factors

Due to relatively low Al content and enrichment in Cd, Hg, Bi, Cu, Mo, Pb, Sb and Sn (partly due to atmospheric deposition) in humus, the EFs medians except for REE and alkali elements are higher when related to element contents in soil (mainly in the subsoil) than to that in humus. Elements with no to slight enrichment in fronds were Ag, As, Bi, Cr, Fe, Li, Na, Sb, Sn, Th, U, V and W, mainly if related to the humus element contents. The highest median EFs characterize macronutrients and their analogues (Ba, Ca, Cs, K, Mg, Rb, S, Sr), some micronutrients and toxic elements (Cd, Cu, Hg, Mn, Mo, Zn) and especially REE (La, Ce, Pr, Nd) and Y. Reasons for bioaccumulation of REE in AFF fronds are not clear; however, recent studies admit some beneficial roles of REE in plants (e.g. Kovaříková et al., 2019, and references therein).

Considerable inter-plots EFs variability includes severe enrichment of Ni, Co, Sn and Tl at few sites, and severe enrichments of Cd, Cu, Hg, Mo and Zn at many sites. pH in humus and partly in the topsoil negatively correlated with EFs for many elements (mainly Ca, Cd, Mg) when related to elements in various soil horizons. Significant influence of other site factors on EFs related to humus, topsoil or subsoil was limited to few elements. Potential evaporation had negative effects on all EFs of Rb. Sandstone bedrocks positively affected EFs (related to subsoil) for Fe, Mg, Mn, Na, Ni and Zn, while EFs of Cs, Rb, Tl and U (related to humus) positively correlated with granite bedrocks.

Conclusions

Median EF values showed bioaccumulation of Ca, K, Mg, Mn, Ba, Rb, Y and REEs in fronds of AFF populations across the country. Not considering macronutrients, the greatest median EF values (ca. 100–500) (in relation to humus and normalized by Al) were obtained for Rb, La, Pr, Nd and Ce, while Cu, Zn, Mn, Mo, Ba, Sr, Cd, Cs, Tl and Y have median EFs between 10 and 100. Significant accumulation of the remaining microelements was not indicated (EFs < 10). REEs are accumulated in AFF fronds very strongly in comparison to other little soluble elements like Al; however, from the viewpoint of bioconcentration factors (all median BCFs < 10), AFF cannot be denoted as a hyperaccumulator of any of the trace elements analyzed. Our results indicate that AFF is rather an excluder of Na, Al, Fe and many trace elements (Ag, As, Bi, Cr, Li, Sb, Sn, Th, U, V and W).

Supplementary information

Below is the link to the electronic supplementary material.

Acknowledgements

We thank to two anonymous reviewers for a detailed revision which helped to improve the manuscript.

Author contribution

I.S. organized the research, performed statistical analyses and wrote the original draft. V.P. determined elements by XRF and participated in writing and editing. J.S. determined element concentrations by ICP-MS and M.H. by ICP-OES.

Funding

Open access publishing supported by the institutions participating in the CzechELib Transformative Agreement. Samples analysis gained in projects CZ0074 and No. LM2023073 was supported by the Financial Mechanism of Norway and a fund of the Ministry of Education, Youth and Sports of the Czech Republic, respectively. The compilation of this paper was supported by institutional support IP VÚKOZ 00027073.

Data availability

No datasets were generated or analysed during the current study.

Declarations

Ethics approval

All authors have read, understood and have complied as applicable with the statement on “Ethical responsibilities of Authors” as found in the Instructions for Authors.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  1. Árvay, J., Demková, L., Hauptvogl, M., Michalko, M., Bajčan, D., Stanovič, R., Tomáš, J., Hrstková, M., & Trebichalský, P. (2017). Assessment of environmental and health risks in former polymetallic ore mining and smelting area, Slovakia: Spatial distribution and accumulation of mercury in four different ecosystems. Ecotoxicology and Environmental Safety,144, 236–244. 10.1016/j.ecoenv.2017.06.020 [DOI] [PubMed] [Google Scholar]
  2. Barbieri, M. (2016). The importance of enrichment factor (EF) and geoaccumulation index (Igeo) to evaluate the soil contamination. Geology and Geophysics,5(1), 237. 10.4172/2381-8719.1000237 [Google Scholar]
  3. Barrat, J.-A., Bayon, G., & Lalonde, S. (2023). Calculation of cerium and lanthanum anomalies in geological and environmental samples. Chemical Geology,615, 121202. 10.1016/j.chemgeo.2022.121202 [Google Scholar]
  4. Bau, M., & Koschinsky, A. (2009). Oxidative scavenging of cerium on hydrous Fe oxide: Evidence from the distribution of rare earth elements and yttrium between Fe oxides and Mn oxides in hydrogenetic ferromanganese crusts. Geochemical Journal,43, 37–47. 10.2343/geochemj.1.0005 [Google Scholar]
  5. Burnison, B. K. (1998). Review of bioconcentration, bioaccumulation and Kow techniques. Water Quality Research Journal,33(2), 213–230. 10.2166/wqrj.1998.012 [Google Scholar]
  6. ČGS (2024). Geologická mapa ČR 1: 50 000. (Geological map of the Czech Republic 1 : 50,000). Czech Geological Survey, Prague. Available on-line at https://mapy.geology.cz/geo/
  7. Cornara, L., Roccotiello, E., Minganti, V., Drava, G., De Pellegrini, R., & Mariotti, M. G. (2007). Level of trace elements in Pteridophytes growing on serpentine and metalliferous soils. Journal of Plant Nutrition and Soil Science,170, 781–787. 10.1002/jpln.200720099 [Google Scholar]
  8. Czerwiński, Z., & Pracz, J. (1995). Content of mineral components in the over-ground parts of herb layer plants in the Sphagnogirgensohnii-Piceetum community. Polish Ecological Studies,21(2), 195–204. [Google Scholar]
  9. Eslava-Silva, F. D. J., Muñíz-Díaz de León, M. E., & Jiménez-Estrada, M. (2023). Pteridium aquilinum (Dennstaedtiaceae), a novel hyperaccumulator species of hexavalent chromium. Applied Sciences,13(9), 5621. 10.3390/app13095621 [Google Scholar]
  10. Grosjean, N., Blaudez, D., Chalot, M., Gross, E. M., & Jean, M. L. (2020). Identification of new hardy ferns that preferentially accumulate light rare earth elements: A conserved trait within fern species. Environmental Chemistry,17(2), 191–200. 10.1071/en19182 [Google Scholar]
  11. Güsewell, S. (2004). N: P ratios in terrestrial plants: Variation and functional significance. New Phytologist,164, 243–266. 10.1111/j.1469-8137.2004.01192.x [DOI] [PubMed] [Google Scholar]
  12. Jedynak, L., Kowalska, J., Harasimowicz, J., & Golimowski, J. (2009). Speciation analysis of arsenic in terrestrial plants from arsenic contaminated area. Science of the Total Environment,407(2), 945–952. 10.1016/j.scitotenv.2008.09.027 [DOI] [PubMed] [Google Scholar]
  13. Kaplan, Z., Koutecký, P., Danihelka, J., Šumberová, K., Ducháček, M., Štěpánková, J., Ekrt, L., Grulich, V., Řepka, R., Kubát, K., Mráz, P., Wild, J., & Brůna, J. (2018).Distribution of vascular plants in the Czech Republic. Part 6. Preslia, 90(3), 235–346. 10.23855/preslia.2018.235
  14. Koerselman, W., & Meuleman, A. F. M. (1996). The vegetation N: P ratio: A new tool to detect the nature of nutrient limitation. Journal of Applied Ecology,33(6), 1441–1450. 10.2307/2404783 [Google Scholar]
  15. Kovařiková, M., Tomášková, I., & Soudek, P. (2019). Rare earth elements in plants. Biologia plantarum,63(1), 20–32. 10.32615/bp.2019.003 [Google Scholar]
  16. Krawczyk, J., Letachowicz, B., Klink, A., & Krawczyk, A. (2006). Zróżnicowanie kumulacji metaliciȩżkich w Athyrium filix-femina (L.) ROTH. i Athyrium distentifolium TAUSCH ex OPIZ z Sowiej Doliny i Doliny Łomniczki (Karkonosze Wschodne) oraz ich wykorzystanie do oceny stanu środowiska (The diversity of metal accumulation in Athyrium filix-femina (L.) ROTH. and Athyrium distentifolium TAUSCH ex OPIZ from the Sowia Dolina and Dolina Łomniczko (Eastern Krkonosze Mts.) and the use of these ferns to evaluation of environmental condition. In Polish). Zeszyty Problemowe Postȩpów Nauk Rolniczych,515, 211–217. [Google Scholar]
  17. Larsen, J.A. (1982). Ecology of the Northern Lowland Bogs and conifer forests. Acad. Press, New York – Toronto, p. 117.
  18. Meharg, A. A. (2003). Variation in arsenic accumulation – Hyperaccumulation in ferns and their allies. New Phytologist,157, 25–31. 10.1046/j.1469-8137.2003.00541.x [DOI] [PubMed] [Google Scholar]
  19. Reznicek, A. A., Meusel, H., & Jager, E. J. (1993). Vergleichende Chorologie der Zentraleuropaischen Flora. Brittonia,45(2), 183. [Google Scholar]
  20. Miretzky, P., & Fernandez-Cirelli, A. (2008). Phosphates for Pb immobilization in soils: A review. Environmental Chemistry Letters,6, 121–133. 10.1007/s10311-007-0133-y [Google Scholar]
  21. Musilova, J., Arvay, J., Vollmannova, A., Toth, T., & Tomas, J. (2016). Environmental contamination by heavy metals in region with previous mining activity. Bulletin of Environmental Contamination and Toxicology,97(4), 569–575. 10.1007/s00128-016-1907-3 [DOI] [PubMed] [Google Scholar]
  22. Neite, H., Neikes, N., & Wittig, R. (1991). Verteilung von Schwermetallen im Wurzelbereich und den Organen von Waldbodenpflanzen aus Buchenwäldern. (Distribution of heavy metals in the root area and in organs of herbaceous plants in beech forests. In German). Flora,185, 325–333. 10.1016/S0367-2530(17)30492-9 [Google Scholar]
  23. Parzych, A. (2010). Azot, fosfor i węgiel w roślinności leśnej Słowińskiego parku narodowego w latach 2002–2005. (Nitrogen, phosphorus and carbon in forest plants in the Słowiński national park in 2002–2005, In Polish). Ochrona Środowiskai Zasobów Naturalnych,43, 47–66. [Google Scholar]
  24. Parzych, A., & Astell, A. (2018). Accumulation of N, P, K, Mg and Ca in 20 species of herbaceous plants in headwater riparian forest. Desalination and Water Treatment,117, 156–167. 10.5004/dwt.2018.22202 [Google Scholar]
  25. Parzych, A., & Jonczak, J. (2018a). Comparison of nitrogen and phosphorus accumulation in plants associated with streams and peatbogs in mid-forest headwater ecosystems. Journal of Elementology,23(2), 459–469. 10.5601/jelem.2017.22.3.1527 [Google Scholar]
  26. Parzych, A., & Jonczak, J. (2018b). Bioaccumulation of Macro-and Microelements in Herbaceous Plants in the River Valley. Journal of Ecological Engineering,19(3), 170. 10.12911/22998993/86157 [Google Scholar]
  27. Prats, K. A., Roddy, A. B., & Brodersen, C. R. (2024). Stomatal behaviour and water relations in ferns and lycophytes across habits and habitats. AoB PLANTS,16(4), 1–15. 10.1093/aobpla/plae041 [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Samecka-Cymerman, A., Kolon, K., Stankiewicz, A., Kaszewska, J., Mróz, L., & Kempers, A. J. (2011). Rhizomes and fronds of Athyrium filix-femina as possible bioindicators of chemical elements from soils over different parent materials in southwest Poland. Ecological Indicators,11(5), 1105–1111. 10.1016/j.ecolind.2010.12.010 [Google Scholar]
  29. Srivastava, M., Santos, J., Srivastava, P., & Ma, L. Q. (2010). Comparison of arsenic accumulation in 18 fern species and four Pteris vittata accessions. Bioresource Technology,101(8), 2691–2699. 10.1016/j.biortech.2009.11.070 [DOI] [PubMed] [Google Scholar]
  30. Stapulionytė, A., Lazutka, J.R., Orland, A., Naujalis, J.R., & Krøkje, A. (2018). RAPD analysis of the lady fern (Athyrium filix-femina L.) from industrial and natural recreational areas in Lithuania and Norway. Poster presented at the 7th Baltic Genetics Congress, University of Latvia, Riga. Available at https://www.researchgate.net/publication/328615869_RAPD_analysis_of_the_lady_fern_Athyrium_filix-femina_L_from_industrial_and_natural_recreational_areas_in_Lithuania_and_Norway
  31. Suchara, I., Sucharova, J., Hola, M., Reimann, C., Boyd, R., Filzmoser, P., & Englmaier, P. (2011). The performance of moss, grass, and 1- and 2-year old spruce needles as bio-indicators of contamination: A comparative study at the scale of the Czech Republic. Science of the Total Environment,409, 2281–2297. 10.1016/j.biortech.2009.11.070 [DOI] [PubMed] [Google Scholar]
  32. Suchara, I., Sucharová, J., & Holá, M. (2017). A quarter century of biomonitoring atmospheric pollution in the Czech Republic. Environmental Science and Pollution Research,24(13), 11949–11963. 10.1007/s11356-015-5368-8 [DOI] [PubMed] [Google Scholar]
  33. Tolasz, R., Míková, T., Valeriánová, A., Voženílek, V., et al. (2007). Atlas podnebíČeska / Climate atlas of Czechia. Czech Hydrometeorological Institute and Palacký University in Olomouc. [Google Scholar]
  34. Van, T. K., Kang, Y., Fukui, T., Sakurai, K., Iwasaki, K., Yoshio Aikawa, Y., & Phuong, N. M. (2006). Arsenic and heavy metal accumulation by Athyrium yokoscense from contaminated soils. Soil Science and Plant Nutrition,52(6), 701–710. 10.1111/j.1747-0765.2006.00090.x [Google Scholar]
  35. Vtorova, V.N., & Solntseva, O.N. (1983). Role of herbaceous cover in exchange processes in coniferous forests. Biology Bulletin of the Academy of Science of the USSR 9(3), 222–228. (Translated from Izvestiya Akademii Nauk SSSR, serija Biologicheskaia 9(3): 341–348, 1982).
  36. Xie, Q.-e, Yan, X.-l, Liao, X.-y, & Li, X. (2009). The arsenic hyperaccumulator fern Pteris vittata L. Environmental Science and Technology,43(22), 8488–8495. 10.1021/es9014647 [DOI] [PubMed] [Google Scholar]
  37. Zhang, S. J., Li, T. X., Huang, H. G., Zhang, X. Z., Yu, H. Y., Zheng, Z. C., Wang, Y. D., Zou, T. J., Hao, X. Q., & Pu, Y. (2014). Phytoremediation of cadmium using plant species of Athyrium wardii (Hook.). International Journal of Environmental Science and Technology,11, 757–764. 10.1007/s13762-013-0384-z [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

No datasets were generated or analysed during the current study.


Articles from Environmental Monitoring and Assessment are provided here courtesy of Springer

RESOURCES