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Toxicity level for phytoavailable zinc in

compost±peat substrates

Annette S. Bucher

*

, Manfred K. Schenk

Institute of Plant Nutrition, University of Hannover, HerrenhaÈuser Straûe 2, 30449 Hannover, Germany

Accepted 17 June 1999

Abstract

Petunias were grown in compost±peat substrates with different Zn contents (basic load, 400, 800, and 1600 mg kg±1) in order to identify toxic levels of Zn in plant dry matter and of phytoavailable (CaCl2-extractable) Zn in compost±peat substrates. Yield reduction of petunias was only observed

at an extremely high Zn content (635 mg Zn kg±1 plant d.m.), although chlorosis was evident at lower Zn levels (160 mg Zn kg±1plant d.m.). Thus, the occurrence of Zn-induced chlorosis during

the growth period was chosen as the toxicity parameter. Chlorosis and plant Zn content were reduced by additional Fe supply, although the Fe content of the plants was not affected. During a six week growth period, petunia Zn content and chlorosis increased in the ®rst two and three weeks, respectively, and then decreased, whereas plant Fe content decreased sharply between the second and third week after the start of Zn treatment. Chlorosis ®rst occurred with a plant Zn content of 160 mg kg±1, corresponding to a CaCl2-extractable Zn content in the substrate of 6 mg l±1, which

was identi®ed as the toxicity level for phytoavailable Zn in compost±peat substrates. Taking a safety factor into account, a critical level of 4.5 mg l±1was computed, which should not be exceeded in order to avoid Zn-induced chlorosis.#2000 Elsevier Science B.V. All rights reserved.

Keywords: CaCl2extraction; Fe de®ciency chlorosis; Petuniahybrida; Zn toxicity

Abbreviations: AAS, atomic absorption spectroscopy; d.m., dry matter; EDDHA, ethylenediamine di(o-hydroxyphenylacetic acid); ICP, inductively coupled plasma (spectroscopy); PTFE, polytetra-fluorethylene (Teflon); SD, standard deviation

*

Corresponding author. Tel.:‡49-511-2626; fax:‡49-511-3611.

E-mail address: [email protected] (A.S. Bucher).

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1. Introduction

Composts prepared from green yard waste (grass and vegetative cuttings) and organic waste are often used as a component of substrates for pot and container plants. However, they often contain large amounts of heavy metals (Kehres, 1991), of which Zn is the one with the highest potential toxicity, because of its high concentration and the comparatively high phytoavailability of Zn in the compost. Zn phytoavailability depends on the total Zn content, pH, content of other heavy metals, and the salt content of the substrate (Herms, 1989). With decreasing pH, intensity and selectivity of Zn sorption decrease, resulting in a higher phytoavailability (Herms, 1982). In compost±peat substrates, phytoavail-able Zn contents can be characterized well by CaCl2 extraction (Bucher and

Schenk, 1997).

Zn-induced chlorosis is known to occur with a Zn content of 200 mg kg±1 in sugar beet leaves (Delschen and Werner, 1989) and of 300 mg kg±1for petunias (Alt et al., 1994) and cereals (Merkel and KoÈster, 1976), indicating different susceptibility between plant species. The toxicity level for CaCl2-extractable Zn

in soil and substrates, based on the occurrence of chlorosis, has been shown to vary between 6 mg l±1 for sugar beet (calculated after Delschen and Werner, 1989) and 55 mg l±1 for petunias (Alt et al., 1994).

Zn toxicity-induced chlorosis resembles Fe de®ciency chlorosis (Rufner and Barker, 1984), which can be corrected by Fe supply (Chaney, 1993). Zn may interfere with Fe uptake, translocation or utilization in the leaves (Chaney, 1993). The aim of this paper was to de®ne the toxicity levels for Zn in the plant dry matter of petunias and for CaCl2-extractable Zn in compost±peat substrates.

Further emphasis was laid on the interaction of Zn and Fe with regard to the occurrence of Zn-induced Fe de®ciency chlorosis.

2. Material and methods

The test plant used was the heavy metal-sensitivePetuniahybrida`Express Orchid' (Bucher and Schenk, 1997).

2.1. Growing conditions

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order to maintain the low pH during the growth period. Plants were harvested after 38 (trial I), 56 (trial II), 45 (trial III), 50 (trial IV), and 42 (trial V) days, respectively.

2.2. Treatments

1.Compost trials (trials I±IV). Mixtures of 40 vol% compost and 60 vol% peat were used as substrates. Compost was prepared from green yard waste (grass and vegetative cuttings). Zn sulfate was added before the waste was composted in order to achieve similar Zn forms as in compost made from polluted raw material. Zn addition was varied to match the contents occurring in commercial composts. The target Zn values of the compost±peat substrates (400, 800, 1600 mg kg±1) were not met exactly, as shown in Table 1.

Composting until maturity of the compost lasted for 14.5±19 weeks. In trials I, II, and III, pH was adjusted to 4, 5, 6, and 7 according to buffer curves by using H2SO4 and CaO. Substrates in trial IV were adjusted to pH 4. The target pH

values were obtained on average with an accuracy of‡0.22 and ±0.37 pH units.

During the trials, pH increased on average by about 0.42 units at the time of harvest. Basic fertilization consisted of 200 mg N l±1 substrate given in the form of NH4NO3. No further nutrients were necessary as basic fertilization, since they

were present in the compost. During the growth period, plants were fertigated with a nutrient solution containing (in mg l±1) 75 N, 15.26 P, 91 K, 0.6 Fe, 0.15 B, 0.01 Cu, 0.25 Mn, 0.025 Mo, and 0.05 Zn. In addition to fertilization, 1 mg Fe per plant as solution of Fe-EDDHA was applied once after one week of cultivation as is usual in horticultural practice (‡Fe treatments). Some further treatments were

included which did not receive the additional Fe supply (±Fe treatments). In trial III these ±Fe treatments were only conducted at pH 4 and 6.

2. Peat trial (trial V). The Zn contents of petunias during the growth period were investigated by growing plants in peat with varied Zn supply, with adjusted substrate pH to 5.2 by the addition of 2.5 g CaCO3l±1 peat. Zinc sulfate was

added before potting the plants in order to achieve the target total Zn contents (800, 1600 mg kg±1). In addition, the peat substrate was fertilized with (in mg lÿ1

): 225 N, 150 P, 225 K, 30 Mg, 1.125 Fe, and other micronutrients. Fertigation was the same as for the compost±peat substrates, but no additional Fe was supplied.

2.3. Experimental design and statistics

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Table 1

Target and aqua-regia-soluble Zn contents in the compost±peat substrates and in peat substrate

Target Zn contents (mg kg±1substrate d.m.)

Aqua regia soluble Zn contents (mg kg±1substrate d.m.)a

Trial I

800 975 695 700 675 886

1600 ±b ± ± 1306 1911

a

Average of all treatments with different pH.

b

Treatment in this trial not available.

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2.4. Chemical analysis and observation of plants

The pH in 0.01 M CaCl2solution was determined in all substrates at the start of

the culture and at harvesting. Substrate samples were taken before potting the plants and after drying and grinding, 2.5 g substrate was digested in aqua regia (10.5 ml HCl‡3.5 ml HNO3). Zn in the digest was detected by atomic

absorption spectroscopy (Hoffmann, 1991). Extractable (phytoavailable) Zn contents in substrates were determined by extracting 1 g dried, sieved (2 mm mesh, stainless steel) substrate with 10 ml 0.1 M CaCl2, and shaking for 1 h

(KoÈster and Merkel, 1982).

Plant samples were oven-dried at 60±708C to determine plant dry matter. Dried, ground plant matter was digested under pressure in PTFE vessels with nitric acid. Zn and Fe were analyzed using AAS and ICP. Plants were harvested weekly for chemical analysis for trial V and at the end of the culture for the other trials. Chlorosis of the plants was monitored weekly in all trials and is reported as a percentage of chlorotic plants, without consideration of the severity of chlorosis.

3. Results

No signi®cant effect of Zn supply on plant dry matter yield was found in most trials (see Table 2), except trial IV. In this case, plant dry matter decreased when treated with the highest Zn supply. This occurred with a plant Zn content of 635 mg Zn kg±1 d.m. and a CaCl2-extractable Zn content of 69 mg Zn l±1

compost±peat substrate. The highest Zn contents without yield reduction were 471 mg Zn kg±1 plant d.m. for the plants grown in the compost±peat substrates and 550 mg Zn kg±1plant d.m. for the plants grown in the peat-only substrate at the end of the experiment.

In all trials, Zn toxicity was visible as interveinal chlorosis of the leaves, often as a transient symptom. Fig. 1(a) and (b) show a typical course of chlorosis during the growth period, using trial III as an example. During the ®rst three weeks after the start of Zn treatment, the percentage of chlorotic plants increased drastically. In the second half of the study, chlorosis decreased, resulting in mainly non-chlorotic plants at the end of the culture. Chlorosis was much more severe at pH 4 (Fig. 1(a)) compared to pH 6 (Fig. 1(b)), since the phytoavailable (CaCl2

-extractable) Zn content of the compost±peat substrate was almost ®ve times higher at pH 4. Supply of 1 mg Fe as Fe±EDDHA per plant, as is usual in horticultural practice, reduced chlorosis appreciably at both pH 4 and 6.

Although chlorosis was reduced by additional Fe supply, no signi®cant effect of Fe supply and pH on plant Fe content was observed (Fig. 2(a)). On the other hand, the Zn content in shoots of petunias was signi®cantly (pˆ0.01) reduced by

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increasing pH, since the CaCl2-extractable Zn content of the compost±peat

substrates decreased. No correlation between plant Zn and plant Fe content was observed in the investigated plants.

The occurrence of chlorosis at any time during the growth period was chosen as the parameter for the de®nition of toxicity levels for Zn contents in petunia dry matter and for CaCl2-extractable Zn in compost±peat substrates, since it was the

most sensitive parameter. Summarizing the results of all four compost±peat substrate trials (trials I±IV), chlorosis ®rst occurred at a plant Zn content of 160 mg Zn kg±1d.m., although non-chlorotic plants were observed at higher plant Zn contents (Fig. 3).

For all trials, the plant Zn content of petunias was closely correlated (r2ˆ0.94)

to the CaCl2-extractable Zn content of compost±peat substrates (Fig. 4(a)),

whereas the correlation was not as good (r2ˆ0.67) in the range below 13 mg

CaCl2-extractable Zn l±1 (Fig. 4(b)). Chlorosis ®rst occurred at approximately

6 mg CaCl2-extractable Zn l±1 compost±peat substrate.

In trial V, plant Zn and Fe contents were analyzed and chlorosis estimated at weekly intervals during the growth period. The increase in petunia dry matter

Table 2

Dry matter yield of petunias as in¯uenced by Zn supply (trials I±V)

Zn supply (mg kg±1

substrate d.m.)

Dry matter yield (g plant±1)

pH 4 pH 5 pH 6 pH 7

Trial I

Basic load 2.59aa 2.61a 2.46a 2.47a

400 2.54a 2.62a 2.40a 2.74a

Basic load 3.11a 3.30a 3.07a 2.99a

400 3.09a 3.23a 3.04a 2.87a

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grown in peat with Zn supply was almost linear during the observed period and was unaffected by the Zn level (Fig. 5(a)). Chlorosis did not occur in the basic load treatment but increased with Zn supply to a level where 90% of the plants were chlorotic (Fig. 5(c)). Chlorosis increased during the ®rst three weeks of the growth period and then decreased until the end of the experiment.

The Zn contents of petunias followed a similar course during the growth period (Fig. 5(b)), but the highest plant Zn contents were determined one week before

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maximum chlorosis of plants. Plant Zn content then decreased until the end of the experiment, followed one week later by the decrease in chlorosis. Although plant Zn contents were high during the growth period, no dry matter yield reduction was observed in any of the treatments.

Plant Fe content decreased between the second and third week after the start of Zn treatment to one third of the initial content. The Fe content was at a similar level in all Zn treatments (Fig. 5(d)).

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4. Discussion and conclusions

4.1. Plant yield and chlorosis as in¯uenced by Zn supply

For plants grown in the compost±peat substrates, dry matter reduction was observed at 635 mg Zn kg±1plant dry matter. This is in the upper range of Zn toxicity levels for other crops quoted in the literature. Zn-induced yield depression may occur in a wide range of plant Zn contents, i.e. 150±500 mg Zn kg±1 plant d.m. (Sauerbeck, 1989), depending on the species. ForZea maysandSorghum bicolor,a signi®cant yield reduction has been observed at 500 mg Zn kg±1plant d.m., whereas 360 mg Zn kg±1plant d.m. were tolerated without symptoms (Smilde et al., 1974). Chlorosis occurred at much lower plant Zn contents in petunia dry matter, i.e., at 160 mg Zn kg±1 plant d.m. (Fig. 3) than yield reduction. The toxicity level obtained in our trials is lower than the toxicity levels for Zn-induced chlorosis in sugar beets of 200 mg Zn kg±1plant d.m. (Delschen and Werner, 1989), and for petunias (Alt et al., 1994) and cereals (Merkel and KoÈster, 1976) of 300 mg Zn kg±1 plant d.m. This might be because these toxicity levels were based on the occurrence of chlorosis at the time of harvesting, whereas in our trials the appearance of chlorosis at any time during the growth period was taken into account.

4.2. Chlorosis as in¯uenced by Zn supply and Fe fertilization

It was decided to use the occurrence of chlorosis at any time during the growth period as the toxicity parameter since its appearance was a very sensitive

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parameter, occurring at much lower Zn contents than yield reduction. The observed transient chlorosis resembled Fe de®ciency chlorosis and could be alleviated by Fe supply.

Chlorosis was more severe at lower pH, indicating that chlorosis was induced by Zn, because absolute Fe de®ciency chlorosis increases with increasing pH (reduced Fe availability). Indeed, a higher proportion of Zn was phytoavailable at

Fig. 4. Relationship between Zn content of the substrate (CaCl2method) and Zn content of plants

and toxicity level for the occurrence of Zn-induced chlorosis in compost±peat substrates (data of all compost±peat substrate trials I±IV): (a) all treatments, (b) treatments having less than 13 mg l±1

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lower pH, as shown by the higher amount of CaCl2-extractable Zn at pH 4 than

pH 6 (Figs. 1 and 2).

Morphological evidence of Zn-induced Fe de®ciency chlorosis is supported by the ®ndings that the chloroplast ultrastructure of tomato and spinach showed similar changes in cases of Fe de®ciency and Zn toxicity (Rufner and Barker, 1984).

In the leaves, Zn might alter the subcellular or cellular distribution or availability of Fe (Rosen et al., 1977). Zn may also inhibit reduction of FeIII to FeII, which is the physiologically active form (Olsen et al., 1982). Hence, Zn can interfere with the utilization of Fe in the leaf, perhaps in chlorophyll biosynthesis (Chaney, 1993). Plant Fe contents were not affected by the Zn treatments (Fig. 2(a)) and they were considered as suf®cient, being in the range of 60±300 mg Fe kg±1plant d.m. which is regarded as normal for plant growth (Vose, 1982).

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It is supposed that the additional Fe±EDDHA supply reduced chlorosis (Fig. 1(a) and (b)) due to decreased plant Zn contents (Fig. 2(b)) since the total plant Fe contents were not affected. In a similar manner, Chaney (1993) observed that Zn-induced chlorosis was corrected by spraying FeSO4 or Fe chelates on the leaves.

Greipsson (1995) and Pich et al. (1994) observed similar results with increasing Fe levels in the growth medium and Fe supply decreasing Zn concentrations in all plant organs.

The time courses of plant Zn and Fe contents were examined in trial V, growing petunias in peat with de®ned Zn contents, in order to explain, why Zn-induced chlorosis was a transient symptom during the growth period.

Chlorosis (Fig. 5(c)) displayed a course similar to those in the compost±peat substrate trials (Fig. 1). The observed courses of Fe and Zn contents in petunias during the growth period might be explained by the following: after the start of Zn treatment the plant Zn content increased during the ®rst two weeks due to increased availability of Zn. Plant Fe contents decreased in the third week, leading to chlorosis in the third week. It is assumed that high plant Zn contents resulted in chlorosis of the leaves at decreased plant Fe contents (three weeks after the start of Zn treatment). The decrease in plant Zn and Fe contents with increasing plant dry matter might be interpreted by dilution (Sauerbeck, 1989). Since plant Zn concentration thus decreased until the end of the culture, chlorosis was also reduced, again showing a delay of one week.

4.3. Toxic level of CaCl2-extractable Zn in compost±peat substrates

The toxic level is de®ned as the lowest Zn content in plants or the lowest CaCl2-extractable Zn content in compost±peat substrates resulting in Zn-induced

chlorosis.

The toxic level of 160 mg kg±1 for Zn in petunia dry matter was related to a level of about 6 mg CaCl2 extractable Zn l±1 substrate (Fig. 4(b)). 6 mg CaCl2

-extractable Zn l±1 substrate is in the lower range of toxic levels of CaCl2

-extractable Zn mentioned in the literature, which were also based on the occurrence of chlorosis. To facilitate comparability, literature data in mg kg±1 soil were converted to mg l±1 soil, based on a bulk density of 1.5 kg l±1 soil. At 6 mg CaCl2-extractable Zn l±1 soil, chlorosis has been shown to occur in sugar

beet (Delschen and Werner, 1989). 30 % of the examined cereals showed Zn-induced toxicity symptoms below 10.5 mg CaCl2-extractable Zn l±1 soil

(Merkel and KoÈster, 1976). Birke and Werner (1991) have mentioned a toxic level of 7.5±22.5 mg CaCl2-extractable Zn l±1 soil for different crops. However, for

petunias, a toxic level, based on the occurrence of chlorosis, of 55 mg CaCl2

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A tolerable level of CaCl2-extractable Zn was ®xed as a value which should not

be exceeded in order to avoid Zn-induced chlorosis. Thus, a safety factor of 25% was considered, resulting in a tolerable level of 4.5 mg CaCl2-extractable Zn l±1

compost±peat substrate.

Acknowledgements

The authors thank the Deutsche Bundesstiftung Umwelt and the Deutsche Kompost Handelsgesellschaft for ®nancial support. Composts were prepared by PlanCoTec, Witzenhausen. In addition, we thank Dr. P. Seward (Hydro Agri Deutschland GmbH, DuÈlmen) for valuable comments and correction of the English.

References

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auf mengen und spurenelemente. 7. Mitteilung: Zink. Agribiol. Res. 47, 75±83.

Birke, C., Werner, W., 1991. Eignung chemischer Bodenextraktionsverfahren zur Prognose der Schwermetallgehalte in P¯anzen. In: Sauerbeck, D., LuÈbben, S. (Eds.), Auswirkungen von SiedlungsabfaÈllen auf BoÈden, Bodenmikroorganismen und P¯anzen, Berichte aus der oÈkologischen Forschung 6. KFA-JuÈlich, Germany, pp. 224±288.

Bucher, A.S., Schenk, M.K., 1997. Characterization of phytoavailable zinc in compost±peat substrates Ð comparison of methods. Z. P¯anzenernaÈhr. Bodenk. 160, 595±601.

Chaney, R.L., 1993. Zinc phytotoxicity. In: Robson, A.D. (Ed.), Zinc in Soils and Plants. Kluwer Academic Publisher, Dordrecht, pp. 135±150.

Delschen, T., Werner, W., 1989. Zur Aussagekraft der Schwermetall-Grenzwerte in klaÈrschlamm-geduÈngten BoÈden. 2. Mitteilung: Beitrag zur Ableitung Tolerierbarer 0.1 M CaCl2-loÈslicher Cd

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Greipsson, S., 1995. Effect of iron plaque on roots of rice on growth of plants in excess zinc and accumulation of phosphorus in plants in excess copper or nickel. J. Plant Nutr. 18, 1659± 1665.

Herms, U., 1982. Untersuchungen zur schwermetallloÈslichkeit in kontaminierten boÈden und kompostierten siedlungsabfaÈllen in abhaÈngigkeit von bodenreaktion, redoxbedingungen und stoffbestand. Ph.D. Diss. Christian-Albrechts-UniversitaÈt, Kiel, Germany.

Herms, U., 1989. LoÈslichkeit von Schwermetallen in BoÈden unter variierenden Milieubedingungen. In: Behrens, D., Wiesner, J. (Eds.), Beurteilung von Schwermetallkontaminationen in BoÈden. Dechema, Frankfurt, a.M., Germany, pp. 189±197.

Hoffmann, G., 1991. Die Untersuchung von BoÈden. Methodenbuch 1. VDLUFA-Verlag, Darmstadt, Germany.

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Merkel, D., KoÈster, W., 1976. Nachweis einer Zn ± toxizitaÈt bei kulturp¯anzen durch die bodenuntersuchung mit hilfe der CaCl2-methode. Landwirtsch. Forsch. Kongreûband 33, 274±

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as it relates to Fe chlorosis. J. Plant Nutr. 5, 433±445.

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