Improved cadmium uptake and accumulation in the hyperaccumulator Sedum alfredii: the impact of citric acid and tartaric acid#

Improved cadmium uptake and accumulation in the hyperaccumulator Sedum alfredii : the impact of citric acid and tartaric acid # # first-author †E-mail:linglilulu@gmail.comxyang571@yahoo.com †E-mail:linglilulu@gmail.comxyang571@yahoo.com linglilulu@gmail.com corresp ‡Corresponding Author ‡Corresponding Author †E-mail:linglilulu@gmail.comxyang571@yahoo.com †E-mail:linglilulu@gmail.comxyang571@yahoo.com linglilulu@gmail.com Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China The elucidation of a natural strategy for metal hyperaccumulation enables the rational design of technologies for the clean-up of metal-contaminated soils. Organic acid has been suggested to be involved in toxic metallic element tolerance, translocation, and accumulation in plants. The impact of exogenous organic acids on cadmium (Cd) uptake and translocation in the zinc (Zn)/Cd co-hyperaccumulator Sedum alfredii was investigated in the present study. By the addition of organic acids, short-term (2 h) root uptake of 109 Cd increased significantly, and higher 109 Cd contents in roots and shoots were noted 24 h after uptake, when compared to controls. About 85% of the 109 Cd taken up was distributed to the shoots in plants with citric acid (CA) treatments, as compared with 75% within controls. No such effect was observed for tartaric acid (TA). Reduced growth under Cd stress was significantly alleviated by low CA. Long-term application of the two organic acids both resulted in elevated Cd in plants, but the effects varied with exposure time and levels. The results imply that CA may be involved in the processes of Cd uptake, translocation and tolerance in S . alfredii , whereas the impact of TA is mainly on the root uptake of Cd. Hyperaccumulation Cadmium Organic acid Sedum alfredii Translocation Uptake Introduction 1 The super ability of hyperaccumulators to extract excess metals from soil is being widely studied (Pence et al., 2000 2000 ; Zhao et al., 2006 2006 ; Hanikenne et al., 2008 2008 ), and transformed into a promising and fairly new field of phytoremediation which deals with sites contaminated with toxic metallic elements (Chaney et al., 2005 2005 ). The efficiency of phytoremediation is largely dependent on the total amount of pollutants removed by the plants (Ebbs et al., 1997 1997 ). More information on the processes involved in metal uptake and translocation in plants will shed light on phytoremediation. Metal bioavailability in the soil-plant system is considered to be a key factor controlling plant uptake. Most plants are capable of exudating some low molecular weight organic acids (LMWOAs), such as citric, malic, oxalic, and succinic acids (Dakora and Phillips, 2002 2002 ). These organic acids can react with metal ions in both the soil solution and solid phases (Jones et al., 1994 1994 ; Nigam et al., 2000 2000 ), and increase metal mobility in the rhizospheric environment, thereby improving the phytoavailability of metals to plants (Lopez-Bucio et al., 2000 2000 ; Ma et al., 2001 2001 ). Enhancement of cadmium (Cd) solubility by various organic acids in soils and subsequent metal uptake by plants has been widely reported (Nigam et al., 2000 2000 ; Han et al., 2006 2006 ). Due to its degradable nature, the use of LMWOA can be an efficient alternative to synthetic chelants used in phytoextraction technology. In hyperaccumulator species, organic acid has also been suggested to be involved in tolerance and accumulation of toxic metallic elements (Boominathan and Doran, 2003 2003 ; Kupper et al., 2004 2004 ; Sun et al., 2006 2006 ; Yang et al., 2006 2006 ). In mature and senescent leaves of Thlaspi caerulescens , most of the accumulated Cd was bound by some weak oxygen ligands such as organic acid (Kupper et al., 2004 2004 ). Nearly 13% of the total Cd accumulated in the hairy roots of T . caerulescens was associated with organic acids, and the rest was localized in the cell walls (Boominathan and Doran, 2003 2003 ). Zn was predominantly coordinated and complexed with malate in the aerial parts of Arabidopsis halleri (Sarret et al., 2004 2004 ). Acetic and citric acids (CAs) might be related to Cd hyperaccumulation in leaves of the new Cd hyperaccumulator Solanum nigrum L. (Sun et al., 2006 2006 ). In case of nickel (Ni) hyperaccumulator Thlaspi goesingense , Ni was predominantly located in the vacuole as an organic complex, possibly CA (Kramer et al., 2000 2000 ). Sedum alfredii Hance is one of the recently identified Cd hyperaccumulators native to China (Yang et al., 2004 2004 ; Sun et al., 2008 2008 ), and is of increasing interest for its potential use in phytoextraction (Li et al., 2007 2007 ; Huang et al., 2008 2008 ; Tian et al., 2009 2009 ). Our previous studies suggested an enhanced uptake and translocation of Cd, mostly through symplastic pathways (Lu et al., 2008 2008 ; 2009 2009 ), in this particular plant species. The physiological mechanisms underlying uptake and accumulation of the metal in S . alfredii , however, are still unknown. Exudation of organic acids such as tartaric acid (TA) and oxalic acid has been observed from the roots of the hyperaccumulator S . alfredii under Cd exposure (Li et al., 2007 2007 ). Moreover, Cd in the shoots of hyperaccumulating ecotype (HE) S . alfredii was mainly coordinated with organic acids, mainly malic acid, and also CA (Tian et al., 2011 2011 ). Preliminary experiments showed that exogenous TA and CA application increased Cd uptake and accumulation in plants of S . alfredii , whereas positive effects were not observed for malic acid or oxalic acid. The present study thereby aims to investigate the uptake and translocation of Cd in the hyperaccumulator S . alfredii when supplemented with a range of exogenous CA or TA. This may help to better understand and clarify the role of these two organic acids in the metal accumulation in this plant species, as well as to promote the use of organic acids in phytoremediation of contaminated soils by S . alfredii . Materials and methods 1 Plant materials and growth conditions 2 Seedlings of the hyperaccumulator Sedum alfredii were cultivated hydroponically. Plants were originally obtained from an old plumbum (Pb)/Zn mine area in Zhejiang Province, China, and chosen to grow in non-contaminated soil for several generations to minimize the internal metal contents. Uniform and healthy shoots were selected and cultivated in the basal nutrient solution containing 2.0 mmol/L Ca(NO 3 ) 2 , 0.7 mmol/L K 2 SO 4 , 0.1 mmol/L KH 2 PO 4 , 0.5 mmol/L MgSO 4 , 0.1 mmol/L KCl, 10 μmol/L H 3 BO 3 , 0.5 μmol/L MnSO 4 , 1.0 μmol/L ZnSO 4 , 0.2 μmol/L CuSO 4 , 0.01 μmol/L (NH 4 ) 6 Mo 7 O 24 , 100 μmol/L iron (Fe)-ethylenediaminetetraacetic acid (EDTA). All the chemicals (analytically pure) used in this study were provided by Sinopharm Chemical Reagent Co., Ltd., China. Nutrient solution pH was adjusted daily to 5.5–5.8 with 0.1 mol/L NaOH or HCl. Plants were grown under glasshouse conditions maintaining natural light, day/night temperature 26/20 °C and day/night humidity 70%/85%. The nutrient solution was continuously aerated and renewed every three days. Radiotracer 109 Cd experiments 2 Intact roots of four-week old seedlings of S . alfredii were rinsed in deionized water, and then treated with a pretreatment solution containing 2 mmol/L MES-Tris (pH=5.8) and 0.5 mmol/L CaCl 2 (Lu et al., 2008 2008 ). After 12 h of pretreatment, the seedlings were used for two experiments as described subsequently. Effects of organic acids on short-term 109 Cd uptake 3 The plants were transferred to custom-built hydroponic vessels (three seedlings in each 400 ml vessel) containing 109 Cd labeled uptake solution. The uptake solution contained 0.5 mmol/L CaCl 2 , 2 mmol/L MES-Tris (pH=5.8) and 10 or 100 μmol/L CdCl 2 labeled with 109 Cd (2.0 μCi/L). Ten treatments were carried out as summarized in Table 1 1 . 2 Treatment 3 Concentration (μmol/L) Cd TA CA T1 10 0 0 T2 10 10 0 T3 10 100 0 T4 10 0 10 T5 10 0 100 T6 100 0 0 T7 100 10 0 T8 100 100 0 T9 100 0 10 T10 100 0 100 Each treatment was replicated four times. Cd speciation in the nutrient solution was calculated by Visual-Minteq 3.0 (Table S1 S1 ). After 2 h of uptake, the seedlings were quickly rinsed with the unlabeled pretreatment solution, and then transferred to identical vessels containing ice-cold desorption solutions (2 mmol/L MES-Tris, pH=5.8, 5 mmol/L CaCl 2 , and 100 μmol/L CdCl 2 ). After 15 min, the seedlings were separated into roots and shoots, blotted-dried and weighed. Plants were transferred into radioactivity counting vials, and 109 Cd was assayed by gamma spectroscopy (Canberra Packard Auto Gamma 5780). Effects of organic acids on 109 Cd translocation 3 The experimental procedure was similar as described above (Section 2.2.1). The uptake solution contained 0.5 mmol/L CaCl 2 , 2 mmol/L MES-Tris (pH=5.8) and 100 μmol/L CdCl 2 labeled with 109 Cd (2.0 μCi/L). Treatments include CA (0, 10, 50, 100, and 500 μmol/L) or TA (0, 50, 100, 250, and 500 μmol/L), respectively. Fresh 109 Cd-labeled solution was added periodically in the uptake solution to maintain constant Cd concentrations. Each treatment was replicated four times. After 24 h of uptake, the seedlings were desorbed by ice-cold solutions (the same as Section 2.2.1) and harvest. The radioactivity of 109 Cd was quantified in both roots and shoots. Long-term effects of organic acids on Cd accumulation 2 Four-week-old intact seedlings of S . alfredii were treated with 100 μmol/L CdCl 2 , in addition with a range of CA (0, 10, 50, 100, or 500 μmol/L) or TA (0, 50, 100, 250, or 500 μmol/L) in basal nutrient solution (see Section 2.1). Each treatment was replicated three times. Cd speciation in the nutrient solution was calculated by Visual-Minteq 3.0 (Table S2 S2 ). Nutrient solution pΗ was adjusted daily to 5.4 with 0.1 mol/L NaOH. The nutrient solutions with different treatments were continuously aerated and changed every three days. Plants were harvested after 7 or 14 d exposure, and rinsed, separated into roots and shoots, oven-dried and weighed. Dry plant samples (0.1 g) of each treatment were digested with 5.0 ml HNO 3 -HClO 4 (v/v, 4:1), and the digest was transferred to a 50-ml volumetric flask, made up to volume and filtered. Cd concentrations were determined by ICP-MS (Agilent 7500a, USA). Statistical methods 2 All data were statistically analyzed using the SPSS package (Version# 11.0). Differences between treatments were determined by the least significant difference ( P < 0.05) from the analysis of variance (ANOVA). Results 1 Effects of CA or TA on 109 Cd uptake and translocation 2 The effects of CA or TA on 109 Cd influx into the roots of S . alfredii were investigated by adding these two organic acids in the 109 Cd uptake solution. Our previous studies suggested that the 2 h uptake period mostly represented the real Cd influx into the roots (Lu et al., 2008 2008 ). As shown in Fig. 1 1 , at 10 μmol/L Cd, addition of equal molar CA significantly ( P < 0.05) increased 109 Cd influx into the roots of S . alfredii (Fig. 1a 1a ). When plants were exposed to 100 μmol/L Cd, higher 109 Cd influx into the roots was marked ( P < 0.05) with the addition of either low (10 μmol/L) or high (100 μmol/L) CA treatment (Fig. 1b 1b ). As compared with CA, the promoted Cd uptake of roots was only significant by the addition of TA at 100 μmol/L level (Fig. 1b 1b ). Plants were exposed to 10 μmol/L (a) or 100 μmol/L (b) 109 Cd for 2 h, with addition of different levels (0, 10, and 100 μmol/L) of CA or TA. Data points and error bars represent means and standard errors (SEs) of four replicates. Means marked with one asterisks indicate significant difference between treatments and control at P < 0.05. DW: dry weight Elevated 109 Cd contents in both roots and shoots of S . alfredii were noted by the application of exogenous CA or TA (Fig. 2 2 ). After 24 h of uptake, 109 Cd in the roots and shoots of S . alfredii increased by 1.5- and 3.0-fold ( P < 0.05), respectively, in addition with 50 μmol/L CA. However, the effect was less pronounced with elevated CA treatment (500 μmol/L) (Fig. 2a 2a ). Exposure of TA resulted in 109 Cd content elevations as high as 2.0- and 2.5-fold in the roots and shoots, respectively, but no dose-dependent increases were observed (Fig. 2b 2b ). A significant ( P < 0.05) increase in 109 Cd root-to-shoot translocation rate was observed for the addition of CA. For example, up to 85% of 109 Cd taken up was distributed to the shoots in the plants with CA treatments, compared with 75% in those not treated with CA (Fig. 3a 3a ). In response to TA treatments, the 109 Cd translocation rate in S . alfredii increased to some extent, but not reached a significant level (Fig. 3b 3b ). Plants were exposed to 100 μmol/L 109 Cd in nutrition solution for 24 h, with addition of different levels of CA (0, 10, 50, 100, and 500 μmol/L) or TA (0, 50, 100, 250, and 500 μmol/L), respectively. Data points and error bars represent means and SEs of four replicates. Different letters indicate significant difference between different treatments at P < 0.05. DW: dry weight Plants were exposed to 100 μmol/L 109 Cd in nutrition solution for 24 h, with addition of different levels of CA or TA. Data points and error bars represent means and SEs of three replicates. Different letters indicate significant difference between different treatments at P < 0.05 Effects of long-term CA/TA treatments on plant growth 2 Hydroponic experiments were employed to study the long-term growth response of the S . alfredii plants by application of CA and TA under Cd stress (Table 2 2 ). The Cd concentration in the nutrient solution was 100 μmol/L, as the report by Ye et al. ( 2003 2003 ) suggested that HE S . alfredii grew healthy at this Cd level in solution. The results showed that no significant decreases in root biomass were observed in the plants after 14 d of Cd exposure, and CA did not significantly affect root growth (Table 2 2 ). However, stem and leaf biomass decreased markedly ( P < 0.05) in the presence of high TA levels (100–500, 250–500 μmol/L, respectively, for stem and leaf) (Table 2 2 ). When plants were treated with 100 μmol/L Cd for 28 d, root biomass decreased significantly ( P < 0.05) as compared to the control (unstressed cultures). No pronounced effects were observed by the application of either CA or TA. Marked decreases of leaf and stem growth were also noted after 28 d of Cd exposure ( P < 0.05). However, application of low CA level significantly ( P < 0.05) alleviated Cd toxicity. After 28 d of exposure, the stem and leaf biomass of the plants under Cd stress increased by 22.5% and 24.9% ( P < 0.05), respectively, in the presence of 10 μmol/L CA, whereas such effect was not pronounced for TA (Table 2 2 ). Different letters among treatments indicate significant differences at P < 0.05. DW: dry weight 3 Cd (μmol/L) 3 Treatment (μmol/L) 6 Biomass (g DW/plant) 3 14 d 3 28 d Root Stem Leaf Root Stem Leaf 0 0.86±0.08 a 2.45±0.23 a 5.23±0.62 a 1.56±0.15 a 4.91±0.51 a 8.03±0.64 a 12 100 CA 0 0.84±0.03 a 2.36±0.19 a 5.18±0.46 a 1.34±0.09 b 3.51±0.46 b 6.07±0.59 c 10 0.84±0.02 a 2.12±0.16 a 4.81±0.70 a 1.42±0.08 b 4.30±0.59 ab 7.58±0.21 ab 50 0.86±0.04 a 2.32±0.27 a 5.49±0.78 a 1.31±0.10 b 3.83±0.70 b 6.64±0.71bc 100 0.87±0.04 a 2.14±0.22 a 4.66±0.48 a 1.31±0.17 b 3.92±0.46 b 6.06±0.40 c 500 0.84±0.03 a 2.11±0.14 a 4.84±0.54 a 1.33±0.09 b 3.88±0.51 b 5.65±1.18 c TA 0 0.84±0.03 a 2.36±0.19 a 5.18±0.46 ab 1.34±0.09 b 3.51±0.46 b 6.07±0.59 b 50 0.84±0.02 a 2.27±0.08 a 4.97±0.49 ab 1.23±0.12 b 3.78±0.61 b 6.35±0.58 b 100 0.84±0.04 a 1.88±0.13 b 5.44±0.50 a 1.23±0.09 b 3.39±0.33 b 6.19±0.55 b 250 0.82±0.04 a 1.63±0.30 b 4.49±0.06 bc 1.34±0.04 b 3.50±0.56 b 6.33±0.37 b 500 0.82±0.03 a 1.60±0.05 b 3.89±0.27 c 1.35±0.10 b 3.52±0.53 b 6.08±0.29 b Effects of long-term CA/TA treatments on Cd accumulation 2 After 14 d of exposure to 100 μmol/L Cd, a majority of Cd taken up by S . alfredii was distributed to the shoots (Table 3 3 ). With low addition of CA (10–100 μmol/L), Cd increased significantly ( P < 0.05) in shoots, especially leaves, of S . alfredii , whereas the same effect was not found in roots. Exposure of TA resulted in root Cd content increases of up to 2.8-fold ( P < 0.05) and a 1.6-fold increase in Cd in the leaves ( P < 0.05). Different letters among treatments indicate significant differences at P < 0.05. DW: dry weight 3 Treatment (μmol/L) 6 Biomass (g DW/plant) 3 14 d 3 28 d Root Stem Leaf Root Stem Leaf CA 0 464±26 a 4740±221 c 5152±259 b 1096±124 b 4882±154 b 6958±690 b 10 500±20 a 5297±186 ab 7054±335 a 1516±103 b 5288±144 a 8008±473 a 50 448±108 a 5312±135 ab 6596±438 a 3328±344 a 4906±104 b 8410±422 a 100 503±80 a 5439±268 a 6550±764 a 3450±305 a 4998±338 ab 7915±477 a 500 523±52 a 5033±311 bc 5387±736 b 3297±592 a 4862±157 b 6883±431 b TA 0 464±26 b 4740±221 c 5152±259 b 1096±124 b 4882±154 b 6958±690 b 50 1285±65 a 5437±567 a 7439±110 ab 1640±229 b 5084±264 bc 7769±392 bc 100 1193±173 a 5895±135 a 8048±654 a 2268±242 a 5352±83 ab 8202±352 ab 250 404±133 b 5390±199 a 6208±1234 bc 2349±238 a 5624±326 a 8652±332 a 500 567±175 b 4711±222 b 6559±1031 bc 1453±164 bc 5680±106 a 7938±462 ab As Cd exposure time prolonged to 28 d, the addition of CA increased Cd contents in the roots and leaves 3- and 1.5-fold, respectively, but the effect was less pronounced in the stems, as marked increase of Cd in the stems was only noted when 10 μmol/L CA was added (Table 3 3 ). With addition of TA, Cd in the roots, stems, and leaves increased 2.2-, 1.2-, and 1.2-fold, respectively (Table 3 3 ). Regardless of the exposure time (14 or 28 d), no dose-dependent increase of Cd concentration in the plants was noted by the application of either CA or TA, and elevated Cd content was not observed with the treatment of high CA or TA level (500 μmol/L) (Table 3 3 ). The total amount of Cd in the aerial parts of the plants is the key factor for the phytoextraction efficiency. Our results showed that low concentration application of CA or TA was able to increase the total amount of Cd in the shoots of S . alfredii (Fig. 4 4 ). When Cd-treated plants were exposed to 50 μmol/L CA for 14 d, a statistically significant increase ( P < 0.05) of 28% in the Cd accumulation was observed in the shoots of S . alfredii (Fig. 4a 4a ). As treatment time was prolonged to 28 d, the addition of 10 μmol/L CA resulted in enhanced Cd accumulation in the shoots ( P < 0.05), whereas no pronounced effect was noted in plants treated with higher CA levels (Fig. 4a 4a ). Cd accumulation in the shoots of S . alfredii ( P < 0.05) increased by 30% and 50%, respectively, with treatments of 50 or 100 μmol/L TA for 14 d (Fig. 4b 4b ). No marked increase of shoot Cd was observed in plants treated with TA for 28 d (Fig. 4b 4b ). Data points and error bars represent means and SEs of three replicates. Different letters among treatments indicate significant differences at P < 0.05 Discussion 1 LMWOAs are attractive alternatives to synthetic chelants for application in phytoextraction of contaminated environments due to their natural and biodegradable properties (Romkens et al., 2002 2002 ). CA-enhanced phytoextraction of toxic metallic elements from contaminated soil has been previously reported (Turgut et al., 2004 2004 ; Quartacci et al., 2005 2005 ; Jean et al., 2008 2008 ). In this study, elevated Cd accumulation via the application of exogenous CA was observed in the hyperaccumulator S . alfredii , in response to either short-term or long-term application of exogenous CA (Table 3 3 ). The similar impacts of CA on Cd uptake and accumulation in non-accumulator plants have been reported in many papers (Senden et al., 1995 1995 ; Chen et al., 2003 2003 ; do Nascimento et al., 2006 2006 ; Duarte et al., 2007 2007 ). The positive effects of CA on the growth of S . alfredii and its heavy metal uptake and accumulation have been reported by using the pot-culture experiments (Sun et al., 2009 2009 ). Enhanced Cd uptake by CA, however, has been attributed to the increase of the metal mobility due to the decrease of the solution pH, as suggested by Chen et al. ( 2003 2003 ). In this study, the application of CA is enhanced the Cd accumulation in the shoots of S . alfredii (Table 3 3 ), despite the same adjusted solution pH level. This suggests that some other mechanisms, rather than decreased pH in the medium, may also be involved in CA-enhanced Cd uptake in plants. CA-induced elevation of Cd accumulation in the shoots of S . alfredii could be attributed to three processes. Firstly, CA might be involved directly in Cd uptake by the plants, possibly by complexation of the metal, rather than changes in rhizosphere environment. The significant increase of 109 Cd influx into the roots of S . alfredii after 2 h application of exogenous CA (Fig. 1 1 ), supports this point of view. It is also supported by our previous analysis on Cd speciation in the hyperaccumulator S . alfredii (Tian et al., 2011 2011 ), which indicated that 24.9% of Cd in roots was associated with CAs. Moreover, with the addition of CA, a small amount of Cd was presented as complexation of Cd-citrate such as Cd-Citrate-in the uptake solution (Table S2 S2 ). Secondly, citrate has been reported to play an important role in the xylem loading of metals such as aluminium (Al) and Fe (Ma and Hiradate, 2000 2000 ; Durrett et al., 2007 2007 ). Elevated root-to-shoot translocation rate of 109 Cd stimulated by CA (Fig. 3 3 ) suggests that this organic acid may also play an important role in xylem transport of Cd in the hyperaccumulator S . alfredii . Last but not the least, application of CA may also contribute to enhanced Cd accumulation by increasing the storage capacity of Cd in the shoots of S . alfredii . Organic acids have been suggested to play an important role in the metal detoxification processes in the hyperaccumulators (Boominathan and Doran, 2003 2003 ; Kupper et al., 2004 2004 ; Sun et al., 2006 2006 ; Yang et al., 2006 2006 ). In a newly discovered Cd hyperaccumulator Solanum nigrum L., a positive correlation was found between CA and water-soluble Cd in the leaves, suggesting that CA was responsible for the Cd accumulation in the leaves of the plants (Sun et al., 2006 2006 ). Yang et al. ( 2006 2006 ) pointed out that CA might be involved in Zn tolerance and accumulation in the shoots of the Zn/Cd hyperaccumulator S . alfredii . Although it has been suggested that Cd was mainly associated with malic acid in shoots of S . alfredii , still a small proportion (about 9.2%–15.4% in leaves, and 21.7% in stems) of Cd was bound with CA (Tian et al., 2011 2011 ). In contrast with CA, only a few studies have reported on the role of TA in enhanced metal accumulation of plants. For example, Pb accumulation in the seedlings of Zinnia elegans Jacq. was markedly ( P < 0.05) increased by TA (Cui et al., 2007 2007 ). TA excretion by roots, however, has been reported to be positively correlated with the metal stress. Cd accumulation in the Fe-sufficient plants of Solanum nigrum L. had a significant ( P < 0.01) positive correlation with the exudation of TA (Bao et al., 2011 2011 ). TA was one of the two main constituents detected in the root exudates of S . alfredii over the 6 h period, and Cd addition had a significant effect ( P < 0.05) on the concentration of TA secreted by roots (Li et al., 2007 2007 ). However, Li et al. ( 2007 2007 ) also suggested that the secretion of organic acids appeared to be a functional metal resistance mechanism that chelates the metal ions extracellularly, and reduces metal uptake and subsequent stresses on roots. This contrasts with the results observed in this study, in which a pronounced increase of 109 Cd accumulation in plants of S . alfredii was observed in roots of S . alfredii by the addition of exogenous TA (Figs. 1 1 and 2 2 ). Nevertheless, the absence of enhanced root-to-shoot translocation rate by addition of TA suggests that the possible role of TA is mainly on the root uptake of Cd by the plants of S . alfredii . Successful removal of metals from contaminated soils via phytoremediation largely depends on sufficient metal concentrations in the shoots of target species. As highlighted by Ebbs et al. ( 1997 1997 ), the emphasis for phytoremediation should be placed on the total amount of contaminant removed from soil. However, biomass losses caused by the negative effects of chelants on plants may decrease their total metal accumulation capacity (Jean et al., 2008 2008 ), despite the increasing removable metal concentrations by the application of chelants. This study suggested that CA and TA could be potentially be applied to contaminated soils where the hyperaccumulator S . alfredii is planted, since they both have positive effects on total metal accumulation in shoots when properly applied (Fig. 4 4 ). 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Cadmium uptake, translocation and tolerance in the hyperaccumulator Arabidopsis halleri 10.1631/jzus.B1200211 Project supported by the National Natural Science Foundation of China (No. 31000935), the Fundamental Research Funds for the Central Universities (No. 2012FZA6008), and the Department of Science & Technology of Zhejiang Province (No. 2011C22077), China 2012-08-04 2013-01-18 2013-01-17 2022-01-05 Copyright © Zhejiang University and Springer-Verlag Berlin Heidelberg 2013 2013 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 02 14