Elsevier

Aquatic Botany

Volume 61, Issue 1, 1 May 1998, Pages 55-67
Aquatic Botany

Zinc, lead and cadmium accumulation and tolerance in Typha latifolia as affected by iron plaque on the root surface

https://doi.org/10.1016/S0304-3770(98)00057-6Get rights and content

Abstract

The effects of iron plaque on the growth of Typha latifolia L. and its accumulation of zinc (Zn), lead (Pb) and cadmium (Cd) were investigated under field conditions and in nutrient solution cultures in the laboratory. In the field, Zn concentrations (but not Cd) on the root surface were positively related to Fe concentrations on the root surface. In the laboratory, seedlings with and without iron plaque on their roots were exposed to 2.0 and 1.0 μg ml−1 Zn for 3 and 72 days and to 10.0 μg ml−1 Pb and 0.2 μg ml−1 Cd for 48 days. Zn accumulation was similar in seedlings with and without plaque when exposed to 2.0 μg ml−1 Zn for 3 days. Over the longer growth periods there was no significant difference in root and shoot dry weights when seedlings with and without plaque were treated with control or metal solutions. Root lengths both in the control and the Cd solution were significantly shorter in seedlings with plaque than in those without. Zn was absorbed fairly equally on root surfaces with and without plaque; however, roots with plaque absorbed more Pb, but less Cd, than those without. The presence of plaque did not alter Zn, Pb and Cd translocation in seedlings in the nutrient solutions. Most of the Pb and Cd taken up was retained in the roots, whereas most of the Zn taken up was retained in the shoots, suggesting that root tissue rather than the root surface or plaque is the main barrier for Pb and Cd transport. However, plaque may act as an effective Fe reservoir to increase Fe ion concentrations in active cells and then ameliorate metal toxicity.

Introduction

Coatings of iron oxides or hydroxides deposited on roots of plants are called `iron plaque.' Plaque can form on roots of submerged, emergent or terrestrial plants subjected to flooding (Crowder and St.-Cyr, 1991). Field observations have shown that wetland plants which can survive in metal-contaminated soils frequently have iron plaque on their roots (Taylor et al., 1984; Otte et al., 1989, Otte et al., 1991; St.-Cyr and Crowder, 1990; Greipsson and Crowder, 1992). The question therefore arises whether iron plaque improves their performance in some way. It is suggested that iron plaque may act as a barrier to toxic substance uptake, mainly metals, owing to adsorption and immobilization of metals by iron plaque (Taylor and Crowder, 1983a; Otte et al., 1987). It has been reported that the formation of plaque can improve growth and ameliorate copper (Cu) and nickel (Ni) toxicity under mildly toxic conditions of Cu and (or) Ni exposure (Greipsson and Crowder, 1992; Greipsson, 1994). However, different results have been reported when seedlings of Typha latifolia with and without plaque were exposed to Cu and Ni solutions (Ye et al., 1997b).

Typha latifolia L. has colonized a wide range of wetland habitats, including heavy metal polluted areas (McNaughton et al., 1974; Taylor and Crowder, 1983b; Ye et al., 1997a), and can produce iron plaque under field and laboratory conditions (Taylor et al., 1984; Macfie and Crowder, 1987; Ye et al., 1994). The aims of the present experiments were to determine the effect of iron plaque on growth, and zinc (Zn), lead (Pb) and cadmium (Cd) immobilization and accumulation in T. latifolia and to test the hypothesis that plaque can ameliorate metal toxicity. Zn, Pb and Cd were chosen for the study as they are common pollutant heavy metals, affecting plants adversely at fairly low concentrations. The novelty of the work presented here is that all experiments were performed using seedlings of T. latifolia, a plant which hitherto had been extremely difficult to culture from seed. Earlier work on iron plaque and metal effects in Typha have employed plantlets regenerated from rhizome fragments where `carry-over' effects may be significant, and where only adventitious roots have thus been involved (e.g. Taylor and Crowder, 1983b; Taylor et al., 1984).

Section snippets

Materials and methods

For field studies, roots of T. latifolia were collected from a small pond receiving metal-enriched drainage water from factories including a cutlery works in Sheffield, UK, in October 1994. The fine (oven-dried) sediment in this pond contained about 900 μg g−1 total Zn, 430 μg g−1 Pb, 9 μg g−1 Cd and 107 000 μg g−1 Fe. Roots were washed gently with tap water and then with deionized water three times. Some had heavy plaque but others were white. According to the differing extent of plaque formation, the

Field measurements

The concentrations of Fe, Mn, Zn and Cd on the root surfaces (in DCB-extracts) were calculated on the basis of μg metal g−1 root d.m. (the concentration of Pb on the root surface was not detectable), and the results of their correlation analyses are presented in Fig. 1. The amounts of Zn adsorbed on the root surfaces were significantly correlated (p <0.05) with the amount of Fe on the roots. However, Cd concentrations on the roots were not significantly correlated with Fe concentrations on the

Discussion

The results from the long-term hydroponic experiments conform with our earlier findings with different metals (Cu and Ni), and showed that plaque was not advantageous for the growth of seedlings in both control and metal solutions and for metal tolerance of T. latifolia (Ye et al., 1997b).

In the 2.0 μg ml−1 Zn solution (3 days), plaque appears to reduce Zn toxicity and protects seedling growth. However, the metal analyses (Table 1) do not show that plaque reduces Zn translocation from roots to

Conclusions

  • 1.

    Iron plaque had no advantageous effect on the growth of seedlings of T. latifolia both in control and Zn, Pb and Cd treatment solutions, and on their metal tolerance under hydroponic conditions.

  • 2.

    Roots, both with plaque and without plaque, were able to adsorb metals on their surface. However, plaque on the root surface was not the main barrier to Zn, Pb and Cd uptake and translocation, root tissue being the chief barrier for Pb and Cd but not for Zn.

Acknowledgements

This study was supported by a Postgraduate Scholarship from the University of Sheffield, UK; the Research Grants Council of University Grants Committee, Hong Kong and the Research Committee, Hong Kong Baptist University, Hong Kong.

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    Present address: Department of Biology, Hong Kong Baptist University, Kowloon Tong, Hong Kong, PR China.

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