Impact Factor 3.678

The world's most-cited Plant Sciences journal

Original Research ARTICLE

Front. Plant Sci., 09 February 2016 | https://doi.org/10.3389/fpls.2016.00128

Characterization of Zinc and Cadmium Hyperaccumulation in Three Noccaea (Brassicaceae) Populations from Non-metalliferous Sites in the Eastern Pyrenees

Soledad Martos1*, Berta Gallego1, Llorenç Sáez2, Javier López-Alvarado2, Catalina Cabot3 and Charlotte Poschenrieder1
  • 1Plant Physiology Laboratory, Bioscience Faculty, Universitat Autònoma de Barcelona, Barcelona, Spain
  • 2Botany Laboratory, Bioscience Faculty, Universitat Autònoma de Barcelona, Barcelona, Spain
  • 3Biology Department, Universitat de les Illes Balears, Palma de Mallorca, Spain

The Southern slope of the Pyrenees is the meridional limit for the distribution of several Noccaea populations. However, the systematic description of these populations and their hyperaccumulation mechanisms are not well established. Morphological and genetic analysis (ITS and 3 chloroplast regions) were used to identify Noccaea populations localized on non-metallicolous soils during a survey in the Catalonian Pyrenees. Cd and Zn concentrations were analyzed in soils and plants both sampled in the field and grown hydroponically. The expression of selected metal transporter genes was assessed by quantitative PCR. The populations were identified as Noccaea brachypetala (Jord.) F.K. Mey by conspicuous morphological traits. Principal component analysis provided a clear separation among N. brachypetala, Noccaea caerulescens J. Presl & C. Presl and Noccaea occitanica (Jord.) F.K. Mey., three Noccaea species reported in the Pyrenees. Contrastingly, ITS and cpDNA analyses were unable to clearly differentiate these taxa. Differences in the expression of the metal transporter genes HMA3, HMA4, and MTP1 between N. caerulescens and N. brachypetala, and those amongst the N. brachypetala populations suggest differences in the strategies for handling enhanced Cd and Zn availability. This is the first report demonstrating Cd and Zn hyperaccumulation by N. brachypetala both in the field and in hydroponics. This comprehensive study based on taxonomic, molecular, and physiological data allows both the correct identification of this species and the characterization of population differences in hyperaccumulation and tolerance of Zn and Cd.

Introduction

During the last decade metal hyperaccumulating plants have attracted much research interest because of their potential use in clean-up of metal contaminated soils. While the direct use of hyperaccumulators is hampered by the usually low biomass of most of these species, the identification of the mechanisms underlying hyperaccumulation can provide the genetic tools for engineering more efficient plants for phytoremediation (Prasad and Freitas, 2003; Krämer, 2005a).

Noccaea caerulescens is a model plant for studying Zn and Cd hyperaccumulation and huge amount of information on this species is available, especially on the Ganges and Prayon ecotypes (Assunção et al., 2003b; Milner and Kochian, 2008; Halimaa et al., 2014). Other Noccaea species have obtained less attention, especially in mechanistic studies.

The number of species within the genus Noccaea (Brassicaceae) has been estimated in 154 (Al-Shebaz, 2014). Many hyperaccumulate Zn (35 species), some of them accumulate Ni (15 species). Noccaea caerulescens and the closely related N. praecox (Vázquez et al., 1992; Vogel-Mikuš et al., 2005) have been described as Cd hyperaccumulators. Moreover, analysis of herbarium material has revealed hyperaccumulation of Zn and Cd in N. brachypetala (Reeves et al., 2001).

Noccaea caerulescens is one of the most variable and taxonomically difficult species of the genus Noccaea (Koch and German, 2013). These authors remark that the adequate taxonomical category of this species has been largely ignored by an important part of the European studies and its putative distribution and that of similar species is uncertain. The presence of N. caerulescens has been described both on metalliferous and on non-metalliferous soils with a widespread, but uncommon, distribution in Western and Central Europe (Clapham and Akeroyd, 1993). France with nearly 80 listed sites for N. caerulescens has probably the best-known distribution of this species in one country (Reeves et al., 2001). Most of these sites are located in Southwest France, and just two populations are indicated by the authors in the Northern Pyrenees. Spain is the southern limit of this species and three Spanish databases (see Materials and Methods) locate all the known populations in the northern part of the Peninsula (from the west to east: Galicia, Cantabria, Basque Country, Aragon and Catalonia). All the eastern Spanish locations are in the Pyrenees.

According to Koch and German (2013) the limit between N. caerulescens and N. brachypetala is unclear, and some specimens from central and eastern France are either considered as synonyms or as subspecies. Nevertheless, Al-Shebaz (2014) recognizes both taxa as separate species. Meyer (1973) accepted three subspecies for N. brachypetala (subsp. brachypetala, subsp. tatrensis, and subsp. huteri), but the concept should to be revised when considering populations from Central France and Spain (Koch and German, 2013).

In this context, the first aim of this study was to contribute to accurately identify the populations of Noccaea from the eastern Pyrenees based on both morphological features and genetic data. The second aim was to elucidate the ability of the three non-metallicolous Pyrenean populations to accumulate Cd and Zn and to characterize the underlying mechanisms, using as a reference the well-characterized N. caerulescens (Ganges). For this purpose, both field and hydroponic studies were performed. Plant growth and the differential expressions of key metal transporters under Cd and Zn exposure were compared among N. caerulescens Ganges and the Pyrenean populations to link metal tolerance to the molecular bases of metal transport and compartmentation. In this regard, our study addresses the lack of combined taxonomical and physiological studies highlighted by Koch and German (2013).

Revealing the molecular basis of metal transporters in Noccaea populations of the Pyrenees can be of the special interest related to the proposals underlined in different phytoremediation reviews (Krämer, 2005a; Pilon-Smits, 2005). In the last decade the use of genetically modified plants for the extraction of metals and metalloids from the soil has been one of the biotechnological achievements. The main approaches to obtain these cleaning-up plants are the implementation of metal transporters, improved production of enzymes of sulfur metabolism and production of metal-detoxifying chelators-metallothioneins and phytochelatins (Kotrba et al., 2009). Moreover, Bhargava et al. (2012) pointed out that knowing the genetics and biochemistry of metal uptake, transport and storage in hyperaccumulator plants will lead to develop transgenic plants with improved phytoremediation capability. Although there is progress in this field and some plants have been modified with metal transporter genes (Antosiewicz et al., 2014; Iqbal et al., 2015), the achievement of an engineered plant with hyperaccumulation traits ready to be used in phytoextraction technology is still a pending challenge.

Materials and Methods

Plant and Soil Sampling

In order to localize Noccaea species in the southern slope of the eastern Pyrenees a survey based on the information of different databases was performed: (1) Anthos program from the Spanish Royal Botanical Garden (http://www.anthos.es/), (2) Biodiversity Data Bank of Catalonia (BDBC; http://biodiver.bio.ub.es/biocat/) and (3) Flora Atlas of Aragon http://www.ipe.csic.es/floragon/).

Using this database information, the distribution of Noccaea in the Catalonian Pyrenees was transferred on cartography marking all the localizations where the genus has been cited. A first sampling campaign was performed in spring 2011 when 16 out of the 38 described localizations were visited. During the sampling, it was observed that the original distribution of Noccaea is currently reduced and plants of this genus could not be found at most previously cited localizations. Finally, three Noccaea populations were located (Figure 1). Throughout the text these populations will be named as Aneu, Mauri, and Freser. In 2014 another population was detected 11 km north from Freser, in Núria. This population was only included in the morphometric and genetic analysis.

FIGURE 1
www.frontiersin.org

Figure 1. Map of distribution of Noccaea species in the Catalonian Pyrenees. Points indicate the 38 sites where Noccaea (N. brachypetala, N. caerulescens, and N. occitanica) are reported in the databases. Black and red points indicate the 16 sites visited during this survey; red points indicate sites where N. brachypetala populations were found; black points are sites where no Noccaea species could be found.

Fruit bearing plants from Aneu and Mauri populations were excavated together with adjacent soil and transferred to culture pots. After transport to the lab, potted plants were located into a growth chamber and regularly watered until seed ripening. The field-collected plants were used for morphological studies and mineral content analysis. As the Freser population was very small only some seeds were collected and no plants were removed for not disturbing this fragile population. At each site, soil close to the plants was collected in triplicate using an Edelman drill, universal type of 7 cm of diameter (Eijkelkamp, Giesbeek, Netherlands) at a depth of 10 cm.

Morphological Study

Positive identification of the three Pyrenean populations was based on morphological and anatomical observations of collected plants and herbarium specimens from two herbaria of the Botanical Institute of Barcelona (BC) (http://www.ibb.bcn-csic.es/en/documentacio/herbari/) and the University of Barcelona (BCN) (http://crai.ub.edu/es/conoce-el-crai/CeDocBiV). Representative herbarium material examined is listed in the Supplementary Material (Table S1). Morphological characters traditionally used in floristic or taxonomic treatments were examined (Bolòs and Vigo, 1990; Clapham and Akeroyd, 1993; Pujadas, 1993; Bolòs et al., 2005; Al-Shebaz, 2014). Features of gross morphology were studied under a Zeiss binocular stereoscopic microscope.

A total number of 41 specimens (13 for N. caerulescens, 17 for N. brachypetala and 11 for N. occitanica) were used for a morphometric multivariate analysis. Twelve quantitative and continuous characters were selected for their taxonomic discriminating value. The normality of each character was tested using the Shapiro-Wilks statistic (Shapiro and Wilk, 1965) and no transformation was needed for any of the characters. All morphometric analyses were computed using SPSS 15.0 (SPSS, 2006). The analysis based on a correlation matrix (PCA; Sneath and Sokal, 1973) was performed using individuals as OTUs (operational taxonomic units). PCA was used to reduce the overall variation of the 12 characters examined into 2 new uncorrelated components to represent morphological relationships among individual specimens. Data relating to glands were not included in the multivariate analysis as it was impossible to obtain micro-morphological data for all of the 41 specimens reviewed in the morphometric study.

Genetic Data

To establish the genetic affinities of the three Pyrenean populations to Noccaea species described in the region and to related taxa from other sources fresh leaves from the collected Pyrenean plants, dried caulinar leaves from the herbarium specimens, and seeds from our personal collection or purchased from a commercial supplier (B & T World Seeds, Aigues-Vives, France) were used. Detailed information on the corresponding geographical origin and, if applies, the herbarium collection is shown in Supplementary Material (Table S2) along with the gene bank accession numbers.

The total genomic DNA was extracted using the NucleoSpin® Plant II Kit (Macherey-Nagel GmbH & Co. KG, Düren, Germany) according to the manufacturer's instructions. Amplifications of four non-coding regions (ITS1-5.8S-ITS2, trnL-trnF, rpl32-trnL(UAG), and trnQ-5rps16) were conducted using a MJ Mini™ Gradient Thermal Cycler (Bio-Rad Laboratories, California, USA) in a 20 μl reaction with IQ™ supermix (Bio-Rad Laboratories, California, USA). The ITS region was amplified and sequenced using primers ITS1 and ITS4 (White et al., 1990) and the protocol of Likar et al. (2010). All sequences of primers are detailed in the Supplementary Material (Table S3). The trnL-trnF region was amplified and sequenced using the primers c and f (Taberlet et al., 1991). The PCR procedure started at 95°C for 4 min, followed by 35 cycles of denaturation at 93°C for 1 min, annealing at 58°C for 1 min, extension at 72°C for 2 min, and a final extension at 72°C for 10 min. The amplification and sequencing of the rpl32-trnL(UAG) region was performed using the rpl32F and trnL(UAG) as forward and reverse primers, respectively (Shaw et al., 2007). The last chloroplast region, trnQ-5rps16, was amplified and sequenced using the trnQ(UUG) as the forward and rpS16x1 as the reverse primer, respectively (Shaw et al., 2007). The last two regions were amplified by using the program “rp116” (Shaw et al., 2005). All PCR amplicons were checked on 1% agarose, TBE 0.5x gels stained by SYBR® safe. Previous to sequencing, PCR products were purified by enzyme digestion of exonuclease I and Antarctic phosphatase (New England Biolabs, Massachussetts, USA). Sequencing was performed at Bioarray, S.L. (Parque Científico y Empresarial de la UMH, Elche, Alicante, Spain) on a BigDye Terminators v3.1 Cycle Sequencing kit (Applied Biosystems, California, USA) and analyzed on an ABI 3130 Genetic Analyzer (Applied Biosystems, California, USA).

The sequences were edited and aligned using Bioedit Sequence Alignment Editor (version 7.0.7.0) (Hall, 1999); alignment was also checked visually by sequential pair wise comparison (Swofford and Olsen, 1990). Phylogenetic analyses were carried out using the Bayesian method and the software MrBayes 3.1.2 (Huelsenbeck and Ronquist, 2001; Ronquist and Huelsenbeck, 2003). The best-available model of molecular evolution required for Bayesian estimations of phylogeny was selected using the Akaike information criteria (AIC) and Bayesian information criterion (BIC), as implemented in the software jModeltest 0.1.1 (Guindon and Gascuel, 2003; Posada, 2008), which considers nucleotide substitution models that are currently implemented in MrBayes 3.1.2. The GTR model (Tavaré, 1986), with variable base frequencies, was assumed to follow a discrete gamma distribution and was selected as the best-fit model of nucleotide substitution for the cpDNA and ITS-cpDNA combined dataset. For the ITS alignment, the symmetrical model with equal base frequencies and rate variation among sites (SYM+G) was selected (Zharkikh, 1994). Bayesian inference analyses were initiated with random starting trees and were run for 106 generations. Four Markov Chains were run using Markov Chain Monte Carlo (MCMC) principal sample trees. One tree out of every 100 generations was saved, which resulted in 10,000 sample trees. Data from the first 2500 generations were discarded as the “burn-in” period, until values had stabilized prior to the 2500th generation. All sequences are deposited in the EMBL/GenBank/DDBJ Nucleotide Sequence Databases.

Analysis of Field-Collected Soil and Plant Samples

Collected soils at each point were sieved through a 2-mm sieve to homogenize the samples and to remove roots. One gram of homogenized soils were mixed with MQ water and the pH of the resulting aqueous solutions were measured by a pHmeter micropH 2002 (Crison Instruments S.A., Barcelona, Spain). Cd, Co, Cu, Pb, and Zn in soils from the three sampled locations were extracted with aqua regia and analyzed by ICP-MS (Perkin Elmer Inc., ELAN 6000, MA, USA) (Bech et al., 2012). The certified reference material CRM 142 R Light Sandy Soil was included for quality control. Prior to the analysis of root and shoot metal concentrations the field-collected plants from Aneu and Mauri populations were carefully washed and processed as described below. The metal concentrations in plants from Freser were not analyzed as the original population was too small to be sampled.

Hydroponic Studies

To verify metal hyperaccumulation in the three Pyrenean populations identified in this study the well-characterized N. caerulescens J. Presl & C. Presl (ecotype Ganges) was hydroponically grown along with the Pyrenean populations. Germination of seeds of N. caerulescens (Ganges) (B&T World Seeds, Aigues-Vives, France) and field-collected seeds from the three Pyrenean populations was synchronized by treatment with 10−5 M gibberellin at 4°C for 4 days. After germination seedlings were first grown on vermiculite irrigated with 25% strength Hoagland solution (pH 5.5) consisting of 1 mM of Ca (NO3)2, 1.25 mM KNO3, 0.5 mM NH4H2PO4, 0.25 mM MgSO4, 50 μM KCl, 25 μM H3BO3, 2 μM MnSO4, 2 μM Zn SO4, 0.5 μM NH4Mo, 0.5 μM CuSO4, and 20 μM Fe-EDDHA. After 2 weeks the seedlings were individually transferred to plastic pots (100 ml capacity) filled with continuously aerated nutrient solution which was renewed weekly. When plants were 1-month old, 100 μM of ZnSO4 or 1.5 μM of CdCl2 were added to the solution and plants were grown for a further 4-week period. Fifteen plants per species or population and treatment were used in each experiment. The experiment was carried out in a growth chamber with day/night temperature of 25/18°C, photoperiod 12 h light/12 h darkness and PAR 135 μE m−2 s−1.

Growth, Photosynthesis, and Mineral Analysis

Growth was assessed by recording rosette and root dry weight after the plant tissues had been oven dried at 60°C. To reveal possible metal toxicity effects leaf chlorophyll concentrations (CCM-300 chlorophyll content Meter, Opti-Sciences, NH, USA) and chlorophyll fluorescence (Fv/Fm ratio) (JUNIOR-PAM, Heinz Walz GmbH, Germany) were measured. Both parameters were quantified as the average of three independent measurements on fully-expanded leaves. Non-destructive parameters (roots scanning, fluorescence and content of chlorophyll) were measured at the beginning of the treatment (t = 0) and every 2 weeks (t = 2nd and 4th week).

After 4 weeks of metal exposure, plants were separated into roots and shoots, carefully washed with distilled water and oven dried (60°C). The dry material from 10 plants per population and treatment was homogenized to fine powder followed by acid digestion (HNO3: H2O2 69%: 30%, 5:2 v/v) in a hot-block digestion system (SC154-54-Well Hot Block™, Environmental Express, SC, USA). The concentrations of the selected elements (Ca, K, Mg, P, S, and B, Cu, Fe, Mn, Mo, Zn) were determined by ICP-OES (Thermo Jarrell-Ash, model 61E Polyscan, England) (Bech et al., 2012). The certified material BCR 62 Olea europaea was included as a reference material for quality control. The data shown are means of three independently analyzed samples from the homogenized powder.

Expression of Metal Transporter Genes

The expressions of selected metal transporter genes were analyzed in plants treated with Cd or Zn in hydroponics for 1 week as described above. Then five plants from each Pyrenean population and from N. caerulescens (Ganges) were divided into roots and shoots. Parts from each population were collected together and then directly immersed into liquid nitrogen, homogenized to fine powder and stored at –80°C until use. Total RNA of each pool (around 100 mg) was extracted with TRIzol® Reagent (Invitrogen, Molecular Research Center Inc., OH, USA) according to the manufacturer's instructions. RNA extracted was quantified with Nanodrop 2000 (Thermo Scientific, DE, USA) and then adjusted to 1 μg. Quality of RNA was checked by the OD A260/A280 (1.8—2.0) and OD A260/A230 (>1.8). The synthesis of cDNA was developed in a 20 μl reaction volume with iScript™ cDNA Synthesis Kit (Bio-Rad, CA, USA). The cDNA (1:50) was used as a template for quantitative PCRs using iTaq™ Universal SYBR® Green Supermix (Bio-Rad, CA, USA) and reaction was developed on a CFX384 or a CFX 96 Real-Time System (Bio-Rad, CA, USA). The plates were edited by the software CFX manager version 3.1.

The effects of Zn and Cd on the expression of metal transporters HMA3, HMA4, and MTP1 were studied. Previously a trial with the primers described for N. caerulescens was done by a common PCR in order to test if the metal transporters primers fitted to the Pyrenean populations. Amplicons were electrophoresed in a 1% agarose gel and band sizes of N. caerulescens were compared to those obtained for the Pyrenean populations. The amplicons of the four genotypes for the three markers were afterwards sequenced and then aligned. The band sizes for the three Pyrenean populations were similar to N. caerulescens and also the blast showed high similarity among them (Figure S1). This result indicates that the primers designed for N. caerulescens amplified for the same region and are optimal to be used for the Pyrenean populations.

The primers used for the expression of HMA3, HMA4 and MTP1 are detailed in the Supplementary Material (Table S3). The expression of target genes was normalized to the expression level of Tubuline gene. Treatment influence on relative gene expression was calculated by the ratio (Efficiency of the target gene) ΔCT,target(calibrator-test)/(Efficiency of the reference gene) ΔCT,reference(calibrator-test) (Pfaffl et al., 2002). The calculated amplification efficiencies were 90.6% (HMA3), 95.9% (HMA4), 99.5% (MTP1), and 93.2% (Tub). The results are means of three independent samples from the homogenized powder.

Statistics

Continuous data were analyzed by the software Statistica 7.0 (Stat Soft, Inc. OK, USA). Normal distribution was checked and data not adjusting to normal distribution were transformed with logarithm and sinus corrections, before applying parametrical tests, ANOVAs followed by Tukey HSD.

Results

Localization and Identification of Pyrenean Noccaea Populations

During the 2011 survey only three Noccaea populations were found in the Catalonian Pyrenees. From the west to the east, the populations are located close to Estany de Sant Maurici (42°57′80.70″ N, 10°08′98.4″ E; altitude 1950 m, called “Mauri”), in the Vall de l'Àneu (42°76′63.05″ N, 1°05′39.98″ E; altitude 1500 m; called “Aneu”) and in the Vall del Freser (42°38′20.78″ N, 2°21′55.15″ E; altitude 1940 m, called “Freser”) (Figure 1). Aneu and Mauri populations developed below trees on subalpine meadows, with each population constituted by more than 15 specimens. In contrast, at Freser only 2 plants growing on a boundary path were found. This population was not stable throughout the years, as confirmed by later visits to the area. At 2014, a small population was detected in Núria, 11 km north from Freser. This population was only included in the genetic study and morphometric analysis. In the available databases, N. caerulescens is classified as an occasional species and correspondingly it should be widespread in the Pyrenees; but this survey revealed that the current distribution of Noccaea in the Pyrenees is reduced compared to previous information.

Morphological studies (Table 1) comparing the sampled populations with herbarium specimens revealed that three Noccaea species are recognized in the Pyrenees: N. brachypetala, N. caerulescens, and N. occitanica. The morphometric multivariate analysis of 41 specimens identified three separated and independent groups providing integrity to these three species without an overlapping of the characters (Figure 2 and Table S4). This is consistent with the taxonomic treatments given by the “Flora Iberica” (Pujadas, 1993), the “Euro+Med PlantBase” (Markhold, 2011) and the synopsis of the genus Noccaea by Al-Shebaz (2014). The number and quality of the discriminating morphological characters found so far (Table 1A) and the lack of intermediate specimens linking the extreme morphotypes strongly supports the view that these three separate species are present in the Pyrenees. However, all specimens from the four populations we located in our survey were clearly identified as N. brachypetala, while we were unable to locate neither N. caerulescens nor N. occitanica in the studied area. Based on data obtained here together with those from previous publications a detailed morphological description of N. brachypetala is provided on the Table 1B.

TABLE 1
www.frontiersin.org

Table 1. Main morphological differences between Noccaea brachypetala, N. caerulescens, and N. occitanica (A).

FIGURE 2
www.frontiersin.org

Figure 2. Morphometric multivariate analysis based on a correlation matrix (PCA) of 12 taxonomic characters of the three Noccaea species recognized at the Pyrenees.

With regard to genetic data, the aligned matrix for ITS consisted of 21 sequences of 677 bp and 107 parsimony-informative characters. The cpDNA matrix consisted of 21 sequences of 1976 bp and 180 parsimony informative characters. The number of variable sites among N. brachypetala, N. caerulescens subsp. caerulescens, and N. occitanica, using the ITS-cpDNA combined dataset, ranges from 0 for N. brachypetala (populations Freser, Mauri, and Núria) and N. occitanica, to 3 for N. brachypetala (Freser, Mauri and Núria) and N. caerulescens subsp. caerulescens Prayon, and to 8 between N. brachypetala (Aneu) and the rest of the clade containing N. brachypetala, N. caerulescens subsp. caerulescens, and N. occitanica.

Bayesian analyses of ITS, cpDNA, and ITS-cpDNA combined datasets, provided similar topologies except for a significantly supported topological incongruence involving N. rotundifolia (L.) Moench, which was clustered in the ITS tree at the same clade as N. brachypetala and N. caerulescens but outside of this clade in cpDNA tree (trees not shown). Nevertheless, the matrices of ITS and cpDNA were combined due to the improvement in the phylogenetic signal and because the phylogenetic reconstruction of genus Noccaea is out of the aim of this work. Moreover, N. rotundifolia is not a key species in this study. The phylogenetic tree for ITS-cpDNA, with Bayesian posterior probabilities (PP), is shown in the Supplementary Material (Figure S2). Genbank accession numbers for the obtained sequences are generated as part of this study (Table S2).

Metal Concentrations in Soils and N. brachypetala Mother Plants

Concentrations of Cd, Zn, Co, Cu, and Pb in the soil surface layer at Aneu, Freser, and Mauri (Figures 3A,B,E) were within the common range (Kabata-Pendias, 2011). No differences in the low soil metal concentrations between Mauri and Freser were observed, while soils from Aneu had higher contents. Soil pH values were 7.3, 5.9, and 5.2, for Aneu, Freser, and Mauri, respectively. Cd and Zn concentrations in the shoots of field-collected plants were extraordinarily high (Figures 3B,D). Aneu plants accumulated 70 times higher Cd and 18 time higher Zn concentrations than those found in the soil, and Mauri plants had 56 and 19 times higher Cd and Zn concentrations, respectively. In contrast, concentrations of Co, Cu, and Pb were lower in plants than in soils (Figures 3E,F). The bioaccumulation index relating the metal concentrations in the shoots to that of soils revealed the extreme ability of N. brachypetala to hyperaccumulate Zn and Cd (Figure 4A) from these unpolluted soils. However, no differences between the bioaccumulation factors of Aneu and Mauri were found due to the higher soil metal concentrations at Aneu.

FIGURE 3
www.frontiersin.org

Figure 3. Concentrations (μg g−1 dry weight) of Cd (A,B), Zn (C,D), and Co, Cu, and Pb (E,F) in soils (A,C,E) and N. brachypetala populations (B,D,F) sampled on the southern slope of the eastern Pyrenees. Metal concentrations in field collected plants were only analyzed in Aneu and Mauri; Freser population was not collected because of the low number of individuals. Metal concentrations were analyzed by ICP-MS after aqua regia extraction.

FIGURE 4
www.frontiersin.org

Figure 4. Bioaccumulation factors (μg g−1 metal shoot/μg g−1 soil) in field sampled N. brachypetala populations (A); translocation factors (μg metal shoot/μg metal root) in N. brachypetala populations and N. caerulescens (Ganges) grown on hydroponics (B); Cd concentrations (μg g−1) in hydroponically-grown N. brachypetala populations and N. caerulescens (Ganges) (C); Zn concentrations (μg g−1) in hydroponically-grown N. brachypetala populations and N. caerulescens (Ganges) (D). Metal treatments on hydroponic plants were 1.5 μM CdCl2 and 100 μM ZnSO4, controls were without Cd or with 2 μM Zn. Plants were under treatment for 4 weeks. Error bars on columns in (A,B) are standard deviations based on three different ICP-MS analyses from a pool of five collected plants or five soil samples; columns with the same letters (capitals for Cd and lower case for Zn) are statistically not different (Tukey test; p < 0.05). Error bars on (C) and (D) are standard deviations based on three independent ICP analyses from a pool of 10 plants; columns with the same letters (capitals for shoots and lower case for roots) are statistically not different (Tukey test; p < 0.05) Dotted lines indicate threshold for hyperaccumulation.

Growth, Zn, and Cd Accumulation in Hydroponics

The hydroponic experiments confirmed the high capacity of N. brachypetala to hyperaccumulate Zn and Cd and revealed the high Zn and Cd tolerance of these plants. All plants exhibited translocation factors greater than 1.0 (Figure 4B). No differences in the Zn and Cd translocation factors among the three N. brachypetala populations were found. Surprisingly, however, the N. brachypetala populations had higher translocation factors for Zn and Cd than N. caerulescens ecotype Ganges. N. caerulescens accumulated lower root and shoot Zn concentrations than N. brachypetala (Figure 4D). Shoot Cd concentrations were highest in N. brachypetala population Freser, followed by Aneu (Figure 4C). Mauri and Ganges had the lowest shoot Cd concentrations, but clearly above the hyperaccumulation threshold.

The hyperaccumulation of Cd did not affect the plant biomass in any population (Figure 5A). However, high Zn accumulation significantly reduced root and shoot growth in plants from Freser. In contrast, biomass production was stimulated by the high Zn supply in plants from the Mauri population (Figure 5B). Neither chlorophyll concentrations nor chlorophyll fluorescence parameters were affected by the metal treatments (data not shown).

FIGURE 5
www.frontiersin.org

Figure 5. Influence of exposure to 1.5 μM Cd (A) or 100 μM Zn (B) on plant dry biomass (% values relative to controls without Cd (A) or with 2 μM Zn (B) of different N. brachypetala populations and N. caerulescens (Ganges). Values are means ± SD (n = 10). Columns with the same letter are statistically not different (p < 0.05). Dotted lines mark 100%.

HMA4, HMA3, and MTP1 Expression

One week after the Zn or Cd treatment was initiated in the hydroponic study, N. caerulescens (Ganges) and the three N. brachypetala populations showed quite different patterns in the expression of metal transporter genes HMA4, HMA3, and MTP1 (Figure 6). The Zn treatment enhanced the root expression especially of MTP1 and HMA3 in Ganges, but not in Mauri. In Aneu Zn exposure induced a slight enhancement of HMA3 expression in roots. In contrast, in roots from Zn treated plants from Freser more than a seven-fold increase in the expression of HMA3 was observed, while expressions of HMA4 and HMA3 decreased. However, HMA4 expression showed a more than two-fold increase in shoots of Mauri. In Freser the Zn treatment caused a small, but statistically significant enhancement of the expression of HMA4 and HMA3 in shoots. In N. caerulescens Ganges Cd induced a close to two-fold increase in the root expression of HMA4, HMA3 and MTP1. Cd-induced up-regulation of HMA4 and HMA3 was strongest in roots of Aneu achieving values close to eight-fold increase, while MTP1 expression decreased in the roots and increased in the shoots. MTP1 expression was also decreased in the roots of Cd-treated Freser and Mauri, while its shoot expression was substantially enhanced in plants from both populations (Figure 6).

FIGURE 6
www.frontiersin.org

Figure 6. Relative expression analysis of three metal transporters according to Pfaffl method. The expression is expressed as the fold change compared to non-treated plants and normalized by tubulin gene. Plants were grown on a hydroponic system for 1 week under metal treatment of 1.5 μM CdCl2 or 100 μM ZnSO4, control plants were non-exposed to Cd or with 2 μM Zn. Shoot markers expression is represented on the top part of the graphic and root markers expression on the bottom part. Dotted lines mark similar expression (fold change around 1) for treated and control plants; double asterisk indicates over-expression (≥ 1.5) and single asterisk indicates down-regulation (≤ 0.5).

Discussion

According to literature and herbarium records N. brachypetala, N. caerulescens, and N. occitanica are more or less sympatric in the eastern Pyrenees. However, during our 3 year survey of the southern slope we only located 4 Noccaea populations. All of them could be identified as N. brachypetala. This identification is strongly supported by vegetative and reproductive characters (Table 1A, Table S4, and Figure 2) consistent with the taxonomical treatments done by Pujadas (1993), Markhold (2011), and Al-Shebaz (2014). Taking into account the morphometric values from 41 different Noccaea accessions (13 N. caerulescens, 11 N. occitanicum, and 17 N. brachypetala) the PCA analysis was able to clearly separate three groups corresponding to these taxa (Figure 2). According to the Eigenvalues the fruit length/fruit width ratio, the fruit width at apex, the stem width, and the style length/notch length ratio were the most determinant morphological parameters.

To support the morphological study and to clarify the relationships between N. brachypetala, N. caerulescens subsp. caerulescens, and N. occitanica on molecular grounds, a genetic analysis of four different regions was developed, using species-level phylogenetic markers. Some authors have used nuclear ribosomal DNA or chloroplast DNA to clarify the phylogenetic relationships within the Brassicaceae family (Franzke et al., 1998; Koch et al., 1998a,b; Bailey and Doyle, 1999; Koch and Mummenhoff, 2001; Koch and Al-Shehbaz, 2004; Koch et al., 2007), as well as in the genus Thlaspi (Mummenhoff and Koch, 1994; Zunk et al., 1996; Mummenhoff et al., 1997). However, taxonomies within Brassicaceae based on two or more datasets combining nuclear and chloroplast information, as presented here, are not generalized. Unfortunately, and in contrast to the cues from the morphological data, we were unable to detect enough phylogenetic signals to separate the Noccaea species by the genetic tools employed.

The poor genetic variation among the three Noccaea species could be explained by a recent or a rapid species radiation event, as denoted by the presence of short branches in the phylogenetic consensus tree (Figure S2). Moreover, incomplete lineage sorting or the presence of interspecific gene flow, mediated by weak genetic barriers, could be hampering the phylogenetic reconstruction as they act as homogenizing forces. The presence of these phenomena is demonstrated by the divergent positions where different accessions of N. brachypetala and N. caerulescens were recovered in the phylogenetic tree (Figure S2). The hypothesis of incomplete lineage sorting may be a better explanation since gene flow is unlikely in putatively inbreeding plants (Lombi et al., 2000; Besnard et al., 2009). Although, gene flow cannot be discarded especially taking into account that out-crossing rates in N. caerulescens can be much higher than originally thought (Koch et al., 1998b). Nonetheless, higher inbreeding coefficients have been observed in non-metallicolous than in metallicolous populations of N. caerulescens (Dubois et al., 2003).

Noteworthy, Mauri and Freser, non-metallicolous populations of N. brachypetala, were in the same clade as N. caerulescens Prayon, a metallicolous ecotype from heavily polluted soil. In contrast, Aneu from a soil with only slightly enhanced Cd and Zn concentrations was on a close, but different clade (Figure S2). Our data are in contrast with the high degree of genetic differentiation found in several studies for N. caerulescens (Koch et al., 1998b; Dubois et al., 2003; Basic and Besnard, 2006; Jiménez-Ambriz et al., 2007). However, these studies applied population genetics approach, using AFLP/isoenzymes and several individuals per population and, therefore they are not fully comparable. Future work should address this issue using more variable markers, such as AFLP or SSR, and focusing sampling effort on the closest relatives: N. brachypetala, N. caerulescens subsp. caerulescens, and N. occitanica.

In the Pyrenees the presence of these three Noccaea species is usually described in grasslands, meadows, prairies and occasionally in forests (Pujadas, 1993). According to the BDBC database, N. caerulescens is present in 28 UTM grids (10 × 10 km). Surprisingly, during our sampling campaign in 2011 searching 16 out of 38 described sites in databases for the occurrence of Noccaea and in further visits in 2012 and 2014, N. brachypetala was only located at Aneu, Mauri, Freser, and Núria, while neither N. caerulescens nor N. occitania were found. This becomes especially relevant when considering the fact that in the studied herbarium material, only four specimens are dated in the twenty-first century; while the rest of the records, 16, were between 40 and 140 years old. Therefore, based on the herbarium material collected data and on our experience in sampling in the Pyrenean range, it is likely that Noccaea is declining in this zone. Besides increasing tourism and urban activities and enhanced herbivore pressure due to cattle raising. This apparently recent decline of Noccaea could be caused by a low resilience to confront climate change, as this zone of the Pyrenees mountain range is on the southern limit of the distribution area of these species. There is clear evidence that the number of cold days per year has been declining during the last 40 years in the eastern Pyrenees (Morán-Tejeda et al., 2013) and this expectedly may have affected the reproductive fitness of Noccaea species which require vernalization for flowering.

The four populations identified in this study are located in cell N29E01 of the Global Terrestrial Network (GTN) of Forges countries in the Geochemical Atlas of Europe (http://weppi.gtk.fi/publ/foregsatlas/) where soil concentrations between 0.06 and 3.03 mg kg−1 for Cd and between 97 and 398 mg kg−1 for Zn are reported in the Spanish site of the cell. This considerable variability for Zn and Cd soil concentration was also reflected in this study where soils from Mauri and Freser had the same typically low Zn and Cd concentrations of non-metalliferous soils, while at Aneu two times higher concentrations of both metals were observed, along with somewhat higher Pb concentrations. These slightly enhanced metal levels are not due to industrial or mining activities in this zone but of geochemical origin as soils at Aneu are derived from shales.

This natural range in soil Zn and Cd concentrations is of special interest for the investigation of the mechanisms of metal accumulation and tolerance in the metal hyperaccumulating populations occurring on non-metalliferous soil. While intense research has been performed in N. caerulescens and clear population differences in the ability to accumulate and tolerate Zn and Cd have been described in this species (Escarré et al., 2000, 2013; Gonneau et al., 2014; Halimaa et al., 2014), N. brachypetala has been ignored for mechanistic studies. Hyperaccumulation of Zn, Cd, Pb, and/or Ni in N. brachypetala has occasionally been mentioned (Reeves and Brooks, 1983; Reeves et al., 2001; Koch and German, 2013); in all cases based on field or herbarium observations. However, the present data do not support accumulation of Pb by the examined plants. As far as we know, this is the first study not only proving the ability of N. brachypetala to hyperaccumulate both Zn and Cd under controlled-environmental conditions but also addressing population differences in Zn and Cd hyperaccumulation of this species in relation to differences in metal transporter gene expression. In fact, the shoot Zn and Cd concentrations of N. brachypetala plants (Figures 3B,D) growing in their natural habitat on soils with normal metal concentrations (Figures 3A,C) and soil pH values ranging from slightly acidic (Freser and Mauri) to near neutral (Aneu) did not hit the threshold concentrations of 10,000 mg kg−1 Zn and 100 mg kg−1 Cd usually considered for hyperaccumulator species (Baker and Brooks, 1989). Only plants from the Aneu population surpassed 3000 mg kg−1 Zn, the concentration more recently proposed as Zn hyperaccumulation threshold by several authors (van der Ent et al., 2013). However, these thresholds are typically reached or even widely surpassed in hyperaccumulator species growing on metalliferous soils. Here we report abnormally high shoot Cd and Zn concentrations in plants from normal soils, displaying bioaccumulation factors far above unity (Figure 4A).

This along with the results from the hydroponic experiments, where plants from all three N. brachypetala populations exceeded the shoot hyperaccumulation thresholds for Zn and Cd and accumulated higher shoot than root Cd and Zn concentrations, clearly demonstrates the hyperaccumulation character of N. brachypetala according to the more rational criteria recently established by van der Ent et al. (2013).

A further clear demonstration of the high efficiency of these N. brachypetala populations in hyperaccumulating Cd and Zn is the fact that when grown under the same hydroponic conditions these plants accumulated as high (Mauri for Cd) or even higher Cd and Zn shoot concentrations than N. caerulescens Ganges, an ecotype that is considered to be highly efficient in Cd and Zn hyperaccumulation (Ueno et al., 2011). Also root to shoot translocation factors for Zn and Cd were higher in the N. brachypetala populations than in N. caerulescens (Ganges) (Figure 4B). Noccaea caerulescens Ganges is highly adapted to metalliferous soils rich in Zn, and Cd (Lombi et al., 2000). Previous investigations have shown that N. caerulescens populations from non-metalliferous soils may accumulate higher Zn and Cd concentrations than those from metalliferous habitats (Escarré et al., 2000). This may be due to lower capacity for root vacuolar storage of metals leading to less exclusion from the transpiration stream. However, N. caerulescens populations from Zn-rich soil may exhibited higher Zn tolerance, than population from non-metalliferous; e.g., N. caerulescens plants from non-metalliferous soil but not those from the metalliferous substrate registered chlorosis when exposed to 50–100 μM of Zn (Assunção et al., 2003a). Despite the fact that the N. brachypetala populations described here developed on soils with less than 1 mg kg−1 Cd, all their offspring when hydroponically grown tolerated the accumulation of more than 200 μg g−1 Cd dry weight in their shoot tissues without any growth reduction, chlorophyll decrease, or influence on photosynthetic capacity. Root development was also not affected in N. brachypetala (data not shown). All N. brachypetala populations, excepting Freser, seem to tolerate exposure to 100 μM Zn as well as N. caerulescens (Ganges) (Figure 5). Nonetheless, further studies using higher external Zn concentrations are required to determine the Zn toxicity thresholds for the Aneu and Mauri populations. Freser was the most Zn sensitive population. Accumulation of more than 12,000 μg g−1 dry weight Zn in the shoots and more than 3000 μg g−1 Zn in the roots caused a significant decrease in biomass production in Freser.

Enhanced expression of metal transporter genes in combination with constitutively high amounts of both metal ligands with low to moderate binding strength such as histidine, nicotianamine, and organic acids, and antioxidants like phenolics and/or glutathione, are key factors for save metal transport to the shoots and metal compartmentation in the leaves in hyperaccumulating species (Tolrà et al., 1996; Freeman et al., 2005; Krämer, 2010; Schneider et al., 2013; Kozhevnikova et al., 2014). The expression of genes coding for metal transporters is regulated among others by the plant organ and its developmental stage, the metal concentration and the exposure time, and the availability of essential mineral nutrients (Küpper and Kochian, 2010).

Here we found differences in the expression of selected metal transporter genes amongst non-metallicolous populations of N. brachypetala and between N. brachypetala and N. caerulescens ecotype Ganges in response to the exposure to moderately high Cd and Zn concentrations. We focused our interest on MTP1, HMA3, and HMA4. The physiological and molecular basis of these genes are well-described for being related to Zn/Cd tolerance in different hyperaccumulator plants (Dräger et al., 2004; Ueno et al., 2011; Craciun et al., 2012). NcHMA4 is expressed throughout the vascular system with highest expression in the crown and has been identified as a key player in both hyperaccumulation and hypertolerance of Zn and Cd (Hanikenne et al., 2008; Craciun et al., 2012). HMA4 in roots seems responsible for xylem loading facilitating root to shoot metal transport (Hanikenne and Nouet, 2011). In N. caerulescens the transporter is localized in all leaf tissues (O'Lochlainn et al., 2011) and may help to transfer Zn from the xylem to the epidermal cells. Zinc compartmentation into the vacuole by the tonoplast transporter MTP1 may explain Zn tolerance in A. halleri (Krämer, 2005b). MTP1 expression is also constitutively higher in the hyperaccumulating N. caerulescens than in the non-hyperaccumulating Thlaspi arvense (Assunção et al., 2001). Compartmentation of Cd into vacuoles is achieved by the tonoplast transporter HMA3 and a higher expression of NcHMA3 is required for Cd hypertolerance in the Cd-hyperaccumulating ecotype Ganges of N. caerulescens (Ueno et al., 2011).

Here we observed that the constitutive shoot expressions of HMA4 and HMA3 were substantially higher in N. caerulescens Ganges than in N. brachypetala (Figure S3). This is not surprising as N. caerulescens ecotype Ganges is highly adapted to metalliferous soils heavily polluted by Zn and Cd, while our N. brachypetala populations were from unpolluted sites. Noteworthy, Freser displayed higher root expression of HMA4 under control conditions than Ganges (Figure S3). This is in accordance with the huge Zn shoot accumulation in this population. Faster translocation of metals from root to shoots in non-metallicolous than in metallicolous populations has previously been observed in both N. caerulescens and A. halleri accessions (Meerts and van Isacker, 1997; Bert et al., 2000; Assunção et al., 2001).

However, exposure to moderately high concentrations of Zn or Cd induced considerable differences in the expression patterns of the selected metal transporter genes among the non-metallicolous populations and between N. brachypetala and N. caerulescens. Different expression levels and the ecotype differences in metal uptake, transport, and tolerance in metal hyperaccumulating species like N. caerulescens or Arabidopsis halleri can be brought about by increased copy number of genes involved in Zn and Cd transport and compartmentation; but altered cis-regulation may be equally or even more important, at least in case of HMA4, which is demonstrated by studies with individual endogenous N. caeruelescens promoters (O'Lochlainn et al., 2011; Iqbal et al., 2013), and confirmed by “selection footprint analysis” (Hanikenne et al., 2013).

The differences in the relative expression of the three metal transporter genes MTP1, HMA3, and HMA4 observed here, support the view of differences in the management of excess Zn and Cd amongst the studied species and populations (Figure 6). In N. caerulescens Ganges root vacuolar storage of Zn and Cd was apparently favored by up-regulation of MTP1 and HMA3 in the roots while the constitutively high shoot expression (Figure S3) did not change under the relatively mild stress conditions of this study (Figure 6). Amongst the N. brachypetala populations the high constitutive expression of HMA4 in roots of Freser indicates high xylem loading; this high root expression level is maintained under Cd exposure and considerably enhanced in the shoots. In fact, Freser accumulated and tolerated the highest Cd shoot and root concentrations (Figure 4). Contrastingly, this population was rather sensitive to Zn (Figure 5). So the strong up-regulation of the Zn vacuolar transporter MTP1 observed in the roots of Freser exposed to excess Zn for 1 week (Figure 6) did not lead to an efficient detoxification and restriction of Zn transport to the shoots in the longer term, as shown by the tissue concentration values determined after 4 weeks of exposure. In contrast, Mauri was Zn tolerant as indicated by the Zn-induced growth enhancement (Figure 5). Opposed to the other specimens, Mauri maintained or even reduced the root expression of HMA3, HMA4, and MTP1 and exhibited the highest up-regulation of shoot HMA4 under both Zn and Cd exposure (Figure 6). Zinc-induced changes in expression patterns in Aneu were similar to those found in Ganges. However, Cd supply caused a strong up-regulation of HMA3 and HMA4 in roots and of MTP1 in shoots, while expression of MTP1 was significantly reduced in the roots. These changes may favor Cd storage in the roots and Zn transport to the shoots under Cd stress. Taken together our results suggest differences amongst the hyperaccumulating N. brachypetala populations in the strategies for handling enhanced Cd and Zn availability: restriction of Cd uptake and enhanced Cd and Zn xylem loading in Mauri with Zn-induced growth stimulation; activation of root vacuolar storage of excess Zn, but insufficient for both restriction of shoot Zn accumulation and avoidance of Zn toxicity in Freser; in Aneu high Zn accumulation in both roots and shoots, high root vacuolar storage of Cd, and decreased root Zn vacuolar storage under Cd exposure favoring Zn translocation to the shoot.

Noccaea brachypetala was clearly identified based on morphological traits, while usual specific genetic markers failed to differentiate the three Noccaea species reported in the eastern Pyrenees. This study confirms for the first time the Zn and Cd hyperaccumulation character of N. brachypetala both in the field and in hydroponics according to criteria by van der Ent et al. (2013). Different expression patterns of metal transporter genes in response to Zn and Cd supply indicate different strategies for handling excess metal ions.

Knowledge about the genetic and molecular mechanisms of heavy metal transport in hyperaccumulators is of fundamental interest for the development of biotechnological tools for phytoremediation of metal contaminated soils. To date, most studies have focused only on two model plants, N. caerulescens and Arabidopsis halleri while close relatives like N. brachypetala have deserved little attention. Here we show for the first time that N. brachypetala is a Cd and Zn hyperaccumulator from non-metallipherous soil that responds to metal exposure by huge activation of metal transporter genes tolerating large concentrations of Zn and Cd in their leaves. The fact that these populations of N. brachypetala develop in the Pyrenees at the southern limit of distribution of Noccaea sp. may provide valuable additional genetic information not only regarding the genetic basis of metal accumulation and tolerance but also of adaptation to the distinctive climatic factors, especially summer heat and drought that will be of relevance for phytoremediation in Mediterranean areas.

Author Contributions

SM contributed to the experimental design, field collected, and lab processed samples, data elaboration, statistics, manuscript writing, and revision. BG contributed to field collected and lab processed samples, data elaboration, manuscript writing, and revision. LS and JL contributed to the data elaboration, statistics, and manuscript writing, and revision. CC and CP contributed to the experimental design, discussion, manuscript writing, and revision. All authors read and approved the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

Funded by the Spanish Government (Ministerio de Economía y Competitividad; projects BFU2010-14873 and BFU2013-42839-R); Berta Gallego was supported by a pre-doctoral grant from UAB. We thank Juan Antonio Calleja who first localized the Freser population, Silvia Busoms and Xavier Marcelino for their help during the field survey, the curators Neus Nualart from the Botanical Institute of Barcelona and Roser Guàrdia from the Herbarium BCN (CeDocBiV, University of Barcelona) for their kind assistance with the herbarium material, Rosa Padilla for her technical assistance during soil and plant mineral analyses, Salvador Bartolomé from the Laboratory of Luminescence and Biomolecular Spectroscopy (UAB) for his help with the qPCRs, and the Institut Cartogràfic i Geològic de Catalunya for authorizing the use of their maps.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fpls.2016.00128

Figure S1. Assay to test the N. caerulescens primers on N. brachypetala. Agarose gels for the amplicons generated by the HMA4 (A), HMA3 (B) and MTP1 (C) primers. Alignments of the purified and sequenced amplicons for HMA4 (D), HMA3 (E), and MTP1 (F) regions. Gray boxes indicate the primer regions. Nc (G) is N. caerulescens ecotype Ganges, and Nb (A, F, and M) are N. brachypetala populations from Aneu, Freser, and Mauri, respectively.

Figure S2. The 50% majority-rule consensus tree obtained from the Bayesian analysis of the combined ITS and cpDNA dataset indicating supported clades (PP > 0.95). Numbers indicate the posterior probabilities (PP). Country names are given as the ISO standard. AV, seeds purchased from B&T World Seeds, Aigues-Vives, France. *Indicates individuals from Herbarium BC. **Indicates individuals from Herbarium BCN.

Figure S3. Relative expression analysis of the three metal transporters according to the ΔCt method. The expression is normalized by tubulin gene as a reference gene. Plants were grown on a hydroponic system for 1 week under metal treatment of 1.5 μM CdCl2 or 100 μM ZnSO4, control plants were non-exposed to Cd or with 2 μM Zn. Shoot markers expression is represented on the top part of the graphic and root markers expression on the bottom part.

Table S1. Studied plant material from the herbaria of the Botanical Institute of Barcelona (BC) and the University of Barcelona (BCN).

Table S2. Genbank accession numbers for the ITS1-ITS4, trnL-trnF, rpl32-trnL(UAG) and trnQ- 5′rps16 regions.

Table S3. Primers used in the experiments.

Table S4. Numerical values of the morphometric multivariate analysis based on the correlation matrix.

References

Al-Shebaz, I. A. (2014). A Synopsis of the Genus Noccaea (Coluteocarpeae, Brassicaceae). Harvard Pap. Bot. 19, 25–51. doi: 10.3100/hpib.v19iss1.2014.n3

CrossRef Full Text | Google Scholar

Antosiewicz, D. M., Barabasz, A., and Siemianowski, O. (2014). Phenotypic and molecular consequences of overexpression of metal-homeostasis genes. Front. Plant Sci. 5:80. doi: 10.3389/fpls.2014.00080

PubMed Abstract | CrossRef Full Text | Google Scholar

Assunção, A. G. L., Bookum, W. M., Nelissen, H. J. M., Vooijs, R., Schat, H., and Ernst, W. H. O. (2003a). Differential metal-specific tolerance and accumulation patterns among Thlaspi caerulescens populations originating from different soil types. New Phytol. 159, 411–419. 10.1046/j.1469-8137.2003.00819.x

CrossRef Full Text | Google Scholar

Assunção, A. G. L., da Costa Martins, P., de Folter, S., Vooijs, R., Schat, H., and Aarts, M. G. M. (2001). Elevated expression of metal transporter genes in three accessions of the metal hyperaccumulator Thlaspi caerulescens. Plant Cell Environ. 24, 217–226. doi: 10.1111/j.1365-3040.2001.00666.x

CrossRef Full Text | Google Scholar

Assunção, A. G. L., Schat, H., and Aarts, M. G. M. (2003b). Thlaspi caerulescens, an attractive model species to study heavy metal hyperaccumulation in plants. New Phytol. 159, 351–360. doi: 10.1046/j.1469-8137.2003.00820.x

CrossRef Full Text | Google Scholar

Bailey, C. D., and Doyle, J. J. (1999). Potential phylogenetic utility of the low-copy nuclear gene pistilata in dycotiledoneous plants: comparison to nrDNA ITS and trnL intron in Sphaerocardamum and other Brassicaceae. Molec. Phylogenet. Evol. 13, 20–30. doi: 10.1006/mpev.1999.0627

PubMed Abstract | CrossRef Full Text | Google Scholar

Baker, A. J. M., and Brooks, R. R. (1989). Terrestrial higher plants which hyperaccumulate metallic elements—a review of their distribution, ecology and phytochemistry. Biorecovery 1, 81–126.

Google Scholar

Basic, N., and Besnard, G. (2006). Gene polymorphisms for elucidating the genetic structure of the heavy-metal hyperaccumulating trait in Thlaspi caerulescens and their cross-genera amplification I Brassicaceae. J. Plant Res. 119, 479–487. doi: 10.1007/s10265-006-0011-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Bech, J., Corrales, I., Tume, P., Barceló, J., Duran, P., Roca, N., et al. (2012). Accumulation of antimony and other potentially toxic elements in plants around a former antimony mine localted in the Ribes Valley (Eastern Pyrenees). J. Geochem. Explor. 113, 100–105. doi: 10.1016/j.gexplo.2011.06.006

CrossRef Full Text | Google Scholar

Bert, V., MacNair, M. R., DeLaguerie, P., Saumitou-Laprade, P., and Petit, D. (2000). Zinc tolerance and accumulation in metallicolous and nonmetallicolous populations of Arabidopsis halleri (Brassicaceae). New Phytol. 146, 225–233. doi: 10.1046/j.1469-8137.2000.00634.x

CrossRef Full Text | Google Scholar

Besnard, G., Basic, N., Christin, P. A., Savova-Bianchi, D., and Galland, N. (2009). Thlaspi caerulescens (Brassicaceae) population genetics by natural variation of soil heavy metal cocncentrations. New Phytol. 181, 974–984. doi: 10.1111/j.1469-8137.2008.02706.x

PubMed Abstract | CrossRef Full Text

Bhargava, A., Carmona, F. F., Bhargava, M., and Srivastava, S. (2012). Approaches for enhanced phytoextraction of heavy metals. J. Environ. Manage. 105, 103–120. doi: 10.1016/j.jenvman.2012.04.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Bolòs, O., and Vigo, J. (1990). Flora dels Països Catalans, Vol. 2. Barcelona: Barcino.

Bolòs, O., Vigo, J., Masalles, R. M., and Ninot, J. M. (2005). Flora Manual dels Països Catalans, 3rd Edn. Barcelona: Edicions 62.

Clapham, A. R., and Akeroyd, J. R. (1993). “Thlaspi L,” in. Flora Europaea, 2nd Edn, Vol. 1, eds T. G. Tutin, N. A. Burges, A. O. Chater, J. R. Edmondson, V. H. Heywood, D. M. Moore et al. (Cambridge: Cambridge University Press), 384–388.

Craciun, A. R., Meyer, C. L., Chen, J., Roosens, N., de Groodt, R., Hilson, P., et al. (2012). Variation in HM4 gene copy number and expression among Noccaea caerulescens populations presenting different levels of Cd tolerance and accumulation. J. Exp. Bot. 63, 4179–4189. doi: 10.1093/jxb/ers104

PubMed Abstract | CrossRef Full Text | Google Scholar

Dräger, D., Desbrosses-Fonrouge, A. G., Krach, C., Chardonnens, A. N., Meyer, R. C., Saumitou-Laprade, P., et al. (2004). Two genes encoding Arabidopsis halleri MTP1 metal transport proteins co-segregate with zinc tolerance and account for high MTP1 transcript levels. Plant J. 39, 425–439. doi: 10.1111/j.1365-313X.2004.02143.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Dubois, S., Cheptou, P. O., Petit, C., Meerts, P., Poncelet, M., Vekemans, X., et al. (2003). Genetic structure and mating systems of metallicolous and nonmetallicolous populations of Thlaspi caerulescens. New Phytol. 157, 633–641. doi: 10.1046/j.1469-8137.2003.00684.x

CrossRef Full Text | Google Scholar

Escarré, J., Lefèbvre, C., Frerot, H., Mahieu, S., and Noret, N. (2013). Metal concentration and metal mass of metallicolous, non metallicolous and serpentine Noccaea caerulescens populations, cultivated in different growth media. Plant Soil 370, 197–221. doi: 10.1007/s11104-013-1618-z

CrossRef Full Text | Google Scholar

Escarré, J., Lefèbvre, C., Gruber, W., Leblanc, M., Lepart, J., Rivière, Y., et al. (2000). Zinc and cadmium hyperaccumulation by Thlaspi caerulescens from metalliferous and nonmetalliferous sites in the Mediterranean area: implications for phytoremediation. New Phytol. 145, 329–437. doi: 10.1046/j.1469-8137.2000.00599.x

CrossRef Full Text

Franzke, A., Pollmann, K., Bleeker, W., Kohrt, R., and Hurka, H. (1998). Molecular systematics of Cardamine and allied genera (Brassicaceae): ITS and non-coding chloroplast DNA. Folia Geobot. 33, 225–240. doi: 10.1007/BF03216204

CrossRef Full Text | Google Scholar

Freeman, J. L., García, D., Kim, D. G., Hopf, A., and Salt, D. E. (2005). Constitutively elevated salicylic acid signals glutathione-mediated nickel tolerance in Thlaspi nickel hyperaccumulators. Plant Physiol. 137, 1082–1091. doi: 10.1104/pp.104.055293

PubMed Abstract | CrossRef Full Text | Google Scholar

Gonneau, C., Genevois, N., Frérot, H., Sirguey, C., and Sterckeman, T. (2014). Variation of trace metal accumulation, major nutrient uptake and growth parameters and their correlations in 22 populations of Noccaea caerulescens. Plant Soil 384, 271–287. doi: 10.1007/s11104-014-2208-4

CrossRef Full Text | Google Scholar

Guindon, S., and Gascuel, O. (2003). A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst. Biol. 52, 696–704. doi: 10.1080/10635150390235520

PubMed Abstract | CrossRef Full Text | Google Scholar

Halimaa, P., Blande, D., Aarts, M. G. M., Tuomainen, M., Tervahauta, A., and Kärenlampi, S. (2014). Comparative transcriptome analysis of the metal hyperaccumulator Noccaea caerulescens. Front. Plant Sci. 5:213. doi: 10.3389/fpls.2014.00213

PubMed Abstract | CrossRef Full Text | Google Scholar

Hall, T. A. (1999). BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp. Ser. 41, 95–98.

Google Scholar

Hanikenne, M., Kroymann, J., Trampczynska, A., Bernal, M., Motte, P., Clemens, S., et al. (2013). Hard selective sweep and ectopic gene conversion in a cluster affording environmental adaptation. PLOS Genet. 9:e1003707. doi: 10.1371/journal.pgen.1003707

PubMed Abstract | CrossRef Full Text | Google Scholar

Hanikenne, M., and Nouet, C. (2011). Metal hyperaccumulation and hypertolerance: a model for plant evolutionary genomics. Curr. Opin. Plant Biol. 14, 252–259. doi: 10.1016/j.pbi.2011.04.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Hanikenne, M., Talke, I. N., Haydon, M. J., Lanz, C., Nolte, A., Motte, P., et al. (2008). Evolution of metal hyperaccumulation requires cis-regulatory changes and triplication of HMA4. Nature 453, 391–396. doi: 10.1038/nature06877

PubMed Abstract | CrossRef Full Text | Google Scholar

Huelsenbeck, J. P., and Ronquist, F. R. (2001). MrBAYES: bayesian inference of phylogenetic trees. Bioinformatics 17, 754–755. doi: 10.1093/bioinformatics/17.8.754

PubMed Abstract | CrossRef Full Text | Google Scholar

Iqbal, M., Ahmad, A., Ansari, M. K. A., Qureshi, M. I., Aref, I. M., Khan, P. R., et al. (2015). Improving the phytoextraction capacity of plants to scavenge metal(loid)-contaminated sites. Environ. Rev. 23, 44–65. doi: 10.1139/er-2014-0043

CrossRef Full Text | Google Scholar

Iqbal, M., Nawaz, I., Hassan, Z., Hakvoort, H. W. J., Bliek, M., Aarts, M. G. M., et al. (2013). Expression of HMA4cDNAs of the zinc hyperaccumulator Noccaea caerulescens from endogenous NcHMA4 promoters does not complement the zinc deficiency phenotype of the Arabidopsis thaliana hma2hma4 double mutant. Front. Plant Sci. 4:404. doi: 10.3389/fpls.2013.00404

CrossRef Full Text | Google Scholar

Jiménez-Ambriz, G., Petit, C., Bourre, I., Dubois, S., Olivieri, I., and Ronce, O. (2007). Life history variation in the heavy metal tolerant plant Thlaspi caerulescens growing in a network of contaminated and noncontaminated sites in southern France: role of gene flow, selection and phenotypic plasticity. New Phytol. 173, 199–215. doi: 10.1111/j.1469-8137.2006.01923.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kabata-Pendias, A. (2011). Trace Elements in Soils and Plants. Boca Raton, FL: CRC Press

Google Scholar

Koch, M. A., and German, D. A. (2013). Taxonomy and systematics are key to biological information: Arabidopsis, Eutrema (Thellungiella), Noccaea and Schrenkiella (Brassicaceae) as examples. Front. Plant Sci. 4:267. doi: 10.3389/fpls.2013.00267

PubMed Abstract | CrossRef Full Text | Google Scholar

Koch, M., and Al-Shehbaz, I. A. (2004). Taxonomic and phylogenetic evaluation of the American “Thlaspi” species: identity and relationship to the Eurasian genus Noccaea (Brassicaceae). Syst. Bot. 29, 375–384. doi: 10.1600/036364404774195566

CrossRef Full Text | Google Scholar

Koch, M., Doves, C., Kiefer, C., Schmickl, R., Klimes, L., and Lysak, M. A. (2007). Supernetwork identifies multiple events of plastid trnF(GAA) pseudogene evolution in the Brassicaceae. Molec. Biol. Evol. 24, 63–73. doi: 10.1093/molbev/msl130

PubMed Abstract | CrossRef Full Text | Google Scholar

Koch, M., and Mummenhoff, K. (2001). Thlaspi s. str. (Brassicaceae) versus Thlaspi sl: morphological and anatomical characters in the light of ITS nrDNA sequence data. Plant Syst. Evol. 227, 209–225. doi: 10.1007/s006060170049

CrossRef Full Text | Google Scholar

Koch, M., Mummenhoff, K., and Hurka, H. (1998a). Molecular biogeography and evolution of the Microthlapsi perfoliatum s.l. polyploid complex (Brassicaceae): chloroplast DNA and nuclear ribosomal DNA restriction site variation. Can. J. Bot. 76, 382–396.

Google Scholar

Koch, M., Mummenhoff, K., and Hurka, H. (1998b). Systematics and evolutionary history of heavy metal tolerant Thlaspi caerulescens in Western Europe: evidence from genetic studies based on isozyme analysis. Biochem. Syst. Ecol. 26, 823–838.

Google Scholar

Kotrba, P., Najmanova, J., Macek, T., Ruml, T., and MacKova, M. (2009). Genetically modified plants in phytoremediation of heavy metal and metalloid soil and sediment pollution. Biotechnol. Adv. 27, 799–810. doi: 10.1016/j.biotechadv.2009.06.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Kozhevnikova, A. D., Seregin, I. V., Erlikh, N. T., Shevyreva, T. A., Andreev, I. M., Verweij, R., et al. (2014). Histidine-mediated xylem loading of zinc is a species-wide character in Noccaea caerulescens. New Phytol. 203, 508–519. doi: 10.1111/nph.12816

PubMed Abstract | CrossRef Full Text | Google Scholar

Krämer, U. (2005a). Phytoremediation: novel approaches to cleaning up polluted soils. Curr. Opin. Biotechnol. 16, 133–141. doi: 10.1016/j.copbio.2005.02.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Krämer, U. (2005b). MTP1 mops up excess zinc in Arabidopsis cells. Trends Plant Sci. 10, 313–315. doi: 10.1016/j.tplants.2005.05.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Krämer, U. (2010). Metal Hyperaccumulation in Plants. Annu. Rev. Plant Biol 61, 517–534. doi: 10.1146/annurev-arplant-042809-112156

PubMed Abstract | CrossRef Full Text | Google Scholar

Küpper, H., and Kochian, L. V. (2010). Transcriptional regulation of metal transport genes and mineral nutrition during acclimatization to cadmium and zinc in the Cd/Zn hyperaccumulator, Thlaspi caerulescens (Ganges population). New Phytol. 185, 114–129. doi: 10.1111/j.1469-8137.2009.03051.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Likar, M., Pongrac, P., Vogel-Mikus, K., and Regvar, M. (2010). Molecular diversity and metal accumulation of different Thlaspi praecox populations from Slovenia. Plant Soil 330, 195–205. doi: 10.1007/s11104-009-0192-x

CrossRef Full Text | Google Scholar

Lombi, E., Zhao, F. J., Dunham, S. J., and McGrath, S. P. (2000). Cadmium accumulation in populations of Thlaspi caerulescens and Thlaspi goesingense. New Phytol. 145, 11–20. doi: 10.1046/j.1469-8137.2000.00560.x

CrossRef Full Text | Google Scholar

Markhold, K. (2011). “Brassicaceae,”– in Euro+Med Plantbase—the Information Resource for Euro-Mediterranean Plant Diversity. Available online at: http://ww2.bgbm.org/EuroPlusMed (Accessed on October 15, 2015).

Meerts, P., and van Isacker, N. (1997). Heavy metal tolerance and accumulation in metallicolous and non-metallicolous populations of Thlaspi caerulescens from continental Europe. Plant Ecol. 133, 221–231. doi: 10.1023/A:1009717619579

CrossRef Full Text | Google Scholar

Meyer, F. K. (1973). Conspectus der “Thlaspi”-Arten Europas, Afrikas und Vorderasiens. Feddes Repert. 84, 449–470.

Google Scholar

Milner, M. J., and Kochian, L. V. (2008). Investigating Heavy-metal Hyperaccumulation using Thlaspi caerulescens as a Model System. Ann. Bot. 102, 3–13. doi: 10.1093/aob/mcn063

PubMed Abstract | CrossRef Full Text | Google Scholar

Morán-Tejeda, E., Herrera, S., López-Moreno, J. I., Revuelto, J., Lehmann, A., and Beniston, M. (2013). Evolution and frequency (1970-2007) of combined temperature-precipitation modes in the Spanish mountains and sensitivity of snow cover. Reg. Environ. Change 13, 873–885. doi: 10.1007/s10113-012-0380-8

CrossRef Full Text | Google Scholar

Mummenhoff, K., Franzke, A., and Koch, M. (1997). Molecular phylogenetics of Thlaspi s.l. (Brassicaceae) based on chloroplast DNA restriction site variation and sequences of the internal transcribed spacers of nuclear ribosomal DNA. Can. J. Bot. 75, 469–482.

Google Scholar

Mummenhoff, K., and Koch, M. (1994). Chloroplast DNA restriction site variation and phylogenetic relationships in the genus Thlaspi sensu lato (Brassicaceae). Syst. Bot. 19, 73–88. doi: 10.2307/2419713

CrossRef Full Text | Google Scholar

O'Lochlainn, S., Bowen, H. C., Fray, R. G., Hammond, J. P., King, G. J., White, P. J., et al. (2011). Tendem quadruplication of HMA4 in the Zinc (Zn) and Cadmium (Cd) hyperaccumulator Noccaea caerulescens. PLoS ONE 6:e17841. doi: 10.1371/journal.pone.0017814

PubMed Abstract | CrossRef Full Text | Google Scholar

Pfaffl, M. W., Horgan, G. W., and Dempfle, L. (2002). A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 29:e45. doi: 10.1093/nar/29.9.e45

PubMed Abstract | CrossRef Full Text | Google Scholar

Pilon-Smits, E. (2005). Phytoremediation. Annu. Rev. Plant Biol. 56, 15–39. doi: 10.1146/annurev.arplant.56.032604.144214

PubMed Abstract | CrossRef Full Text | Google Scholar

Posada, D. (2008). jModelTest: phylogenetic model averaging. Molec. Biol. Evol. 25, 1253–1256. doi: 10.1093/molbev/msn083

PubMed Abstract | CrossRef Full Text | Google Scholar

Prasad, M. N. V., and Freitas, H. M. D. (2003). Metal hyperaccumulation in plants—Biodiversity prospecting for phytoremediation technology. Elect. J. Biotech. 6, 285–321. doi: 10.2225/vol6-issue3-fulltext-6

CrossRef Full Text | Google Scholar

Pujadas, A. (1993). “Thlaspi L,” in Flora Iberica, Vol. IV, Cruciferae-Monotropaceae, eds S. Castroviejo, C. Aedo, C. Gómez-Campo, M. Laínz, P. Montserrat, R. Morales et al. (Madrid: Real Jardín Botánico, CSIC), 255–264.

Reeves, R. D., and Brooks, R. R. (1983). European species of Thlaspi L. as indicators of nickel and zinc. J. Geochem. Explor. 18, 275–283.

Google Scholar

Reeves, R. D., Schwartz, C., Morel, J. L., and Edmondson, J. (2001). Distribution and metal-accumulating behavior of Thlaspi caerulescens and associated metallophytes in France. Int. J. Phytorem. 3, 145–172. doi: 10.1080/15226510108500054

CrossRef Full Text | Google Scholar

Ronquist, F., and Huelsenbeck, J. P. (2003). MrBAYES 3: bayesian phylogenetic inference under mixed models. Bioinformatics 19, 1572–1574. doi: 10.1093/bioinformatics/btg180

PubMed Abstract | CrossRef Full Text | Google Scholar

Schneider, T., Persson, D. P., Husted, S., Schellenberg, M., Gehrig, P., Lee, Y., et al. (2013). A proteomics approach to investigate the process of Zn hyperaccumulation in Noccaea caerulescens (J & C. Presl) F. K.Meyer. Plant J. 73, 131–142. doi: 10.1111/tpj.12022

PubMed Abstract | CrossRef Full Text | Google Scholar

Shapiro, S. S., and Wilk, M. B. (1965). An analysis of variance test for normality (complete samples). Biometrika 52, 591–611. doi: 10.1093/biomet/52.3-4.591

CrossRef Full Text | Google Scholar

Shaw, J., Lickey, E., Beck, J., Farmer, S., Liu, W., Miller, J., et al. (2005). The tortoise and the hare II: relative utility of 21 noncoding chloroplast DNA sequences for phylogenetic analysis. Am. J. Bot. 92, 142–166. doi: 10.3732/ajb.92.1.142

PubMed Abstract | CrossRef Full Text | Google Scholar

Shaw, J., Lickey, E., Schilling, E., and Small, R. (2007). Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in Angiosperms: the tortoise and the hare III. Am. J. Bot. 94, 275–288. doi: 10.3732/ajb.94.3.275

PubMed Abstract | CrossRef Full Text | Google Scholar

Sneath, P. H. A., and Sokal, R. R. (1973). Numerical Taxonomy. Principles and Practice of Numerical Classification. San Francisco, CA: W.H. Freeman & Company.

Google Scholar

SPSS (2006). SPSS for Windows, Version 15.0. Chicago, IL: SPSS Inc.

Swofford, D. L., and Olsen, G. J. (1990). “Phylogeny reconstruction,” in Molecular Systematic, eds D. M. Hillis and C. Moritz (Sunderland, MA: Sinauer), 411–501.

Taberlet, P., Gielly, L., Pautou, G., and Bouvet, J. (1991). Universal primers for amplification of 3 noncoding regions of chloroplast DNA. Plant Molec. Biol. 17, 1105–1109. doi: 10.1007/BF00037152

PubMed Abstract | CrossRef Full Text | Google Scholar

Tavaré, S. (1986). “Some probabilistic and statistical problems in the analysis of DNA sequences,” in Some Mathematical Questions in Biology—DNA Sequence Analysis, ed R. M. Miura (Providence, RI: American Mathematical Society), 57–86.

Tolrà, R., Poschenrieder, C., and Barceló, J. (1996). Zinc hyperaccumulation in Thlaspi caerulescens. II. Influence on organic acids. J. Plant Nutr. 19, 1541–1550.

Google Scholar

Ueno, D., Milner, M. J., Yamaji, N., Yokosho, K., Koyama, E., Zambrano, M. C., et al. (2011). Elevated expression of TcHMA3 plays a key role in the extreme Cd tolerance in a Cd-hyperaccumulating ecotype of Thlaspi caerulescens. Plant J. 66, 852–862. doi: 10.1111/j.1365-313X.2011.04548.x

PubMed Abstract | CrossRef Full Text | Google Scholar

van der Ent, A., Baker, A. J. M., Reeves, R. D., Pollard, A. J., and Schat, H. (2013). Hyperaccumulators of metal and metalloid trace elements: facts and fiction. Plant Soil 362, 319–334. doi: 10.1007/s11104-012-1287-3

CrossRef Full Text | Google Scholar

Vázquez, M. D., Barceló, J., Poschenrieder, C., Mádico, J., Hatton, P., Baker, A. J. M., et al. (1992). Localization of zinc and cadmium in Thlaspi caerulescens (Brassicaceae), a metallophyte that can hyperaccumulate both metals. J. Plant Physiol. 140, 350–355. doi: 10.1016/S0176-1617(11)81091-6

CrossRef Full Text | Google Scholar

Vogel-Mikuš, K., Drobne, D., and Regva, M. (2005). Zn, Cd and Pb accumulation and arbuscular mycorrhizal colonization of penny cress Thlaspi praecox Wulf. (Brassicaceae) from the vicinity of a lead mine and smelter in Slovenia. Environ. Pollut. 133, 233–242. doi: 10.1016/j.envpol.2004.06.021

PubMed Abstract | CrossRef Full Text | Google Scholar

White, T. J., Bruns, T., Lee, S., and Taylor, J. (1990). “Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics,” in PCR Protocols: A Guide to Methods and Applications, eds M. A. Innis, D. H. Gelfand, J. J. Sninsky, and T. J. White (San Diego, CA: Academic Press), 315–322. doi: 10.1016/b978-0-12-372180-8.50042-1

CrossRef Full Text

Zharkikh, A. (1994). Estimation of evolutionary distances between nucleotide sequences. J. Molec. Evol. 39, 315–329. doi: 10.1007/BF00160155

PubMed Abstract | CrossRef Full Text | Google Scholar

Zunk, K., Mummenhoff, K., Koch, M., and Hurka, H. (1996). Phylogenetic relationships of Thlaspi s.l. (subtribe Thlaspidinae, Lepidieae) and allied genera based on chloroplast DNA restriction-site variation. Theor. Appl. Genet. 92, 37.

PubMed Abstract | Google Scholar

Keywords: Noccaea brachypetala, genetic markers, morphometric markers, Zn hyperaccumulator, Cd hyperaccumulator, non-metalliferous soil

Citation: Martos S, Gallego B, Sáez L, López-Alvarado J, Cabot C and Poschenrieder C (2016) Characterization of Zinc and Cadmium Hyperaccumulation in Three Noccaea (Brassicaceae) Populations from Non-metalliferous Sites in the Eastern Pyrenees. Front. Plant Sci. 7:128. doi: 10.3389/fpls.2016.00128

Received: 27 October 2015; Accepted: 23 January 2016;
Published: 09 February 2016.

Edited by:

Shabir Hussain Wani, Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir, India

Reviewed by:

Rufus Lee Chaney, US Department of Agriculture, Agricultural Research Service, USA
Rudra Deo Tripathi, CSIR-National Botanical Research Institute, India

Copyright © 2016 Martos, Gallego, Sáez, López-Alvarado, Cabot and Poschenrieder. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Soledad Martos, soledad.martos@uab.cat