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Open Chemistry

formerly Central European Journal of Chemistry


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Volume 16, Issue 1

Issues

Volume 13 (2015)

New phosphorus biofertilizers from renewable raw materials in the aspect of cadmium and lead contents in soil and plants

P-biofertilizers from waste and Cd and Pb in soil and plant

Magdalena Jastrzębska
  • Department of Agroecosystems, Faculty of Environmental Management and Agriculture, University of Warmia and Mazury in Olsztyn, Plac Łódzki 3, 10-718 Olsztyn, Poland
  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
/ Agnieszka Saeid
  • Corresponding author
  • Department of Advanced Material Technologies, Faculty of Chemistry, Wroclaw University of Science and Technology, Smoluchowskiego 25, 50-372 Wrocław, Poland
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  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
/ Marta K. Kostrzewska
  • Department of Agroecosystems, Faculty of Environmental Management and Agriculture, University of Warmia and Mazury in Olsztyn, Plac Łódzki 3, 10-718 Olsztyn, Poland
  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
/ Sylwia Baśladyńska
  • Department of Advanced Material Technologies, Faculty of Chemistry, Wroclaw University of Science and Technology, Smoluchowskiego 25, 50-372 Wrocław, Poland
  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
Published Online: 2018-02-13 | DOI: https://doi.org/10.1515/chem-2018-0004

Abstract

Recycling phosphorus from waste for fertilization purposes appears to be an alternative for non-renewable sources and a solution for managing harmful products of civilisation. Fertilizers from secondary raw materials are considered to be safe to the environment. This study presents an assessment of the effects of five new biofertilizers made from sewage sludge ash and/or animal bones on the content of cadmium and lead in the soil, in wheat grains and straw (test plant), in the mass of the the accompanying weeds and in the post-harvest residues. Biofertilizers were produced in the form of suspension or granules and activated using Bacillus megaterium or Acidithiobacillus ferrooxidans bacteria. They were tested in four field experiments. The Cd and Pb contents of the soil and plant material were determined using the ICP-MS technique. Similar to superphosphate, new biofertilizers showed no change in the Cd and Pb contents of the soil and plants biomass when applied at amounts up to 80 kg; P2O5 ha−1. Both Cd and Pb in the soil and plants occurred naturally, and the amounts were within the acceptable standards. Biofertilizers from renewable raw materials, with low toxic element contents, are not thought to pose a hazard to the soil and plants when applied in reasonable amounts. They can be a substitute for conventional phosphorus fertilizers.

Keywords: biofertilizers; sewage sludge ash; animal bones; phosphorus solubilizing bacteria; wheat; weeds

1 Introduction

Phosphorus is an essential element for the survival of every organism, and its role in the production of food is outright strategic [1]. Unreasonable management of the primary resources of phosphorus has recently been the subject of numerous scientific and political discussions. Concerns for securing the sources of this element for the future usage are one aspect of the problem; another is the fact that the wastage of phosphorus at the stages of sourcing and during its usage results in water and soil contamination [2]. Even though the recent estimates of global geological resources of phosphorus-containing rocks [3] deny the prevailing (until recently) conviction about its impending exhaustion [4], it does not, however, change their status as non-renewable resources. In addition, natural resources of phosphorus are not distributed uniformly throughout the globe [3]. The European Union (EU) has recently categorised phosphorites in the list of 20 critical raw materials [5]. The EU countries, including Poland, are largely dependent on their import.

Closing the phosphorus cycle, i.e. recycling, appears to be a good solution to both agricultural demand for this element [6] and to the issue of managing the growing amount of the wastes of civilisation [7]. Recycling is one of the ideas providing a basis for the European strategy on sustainable use of phosphorus [2]. Modern proenvironmental technologies for fertilizer production enables the usage of waste as secondary raw materials [8, 9]. Sludge originating from the treatment of municipal wastewater as well as animal bones are considered to be potential renewable phosphorus sources [10, 11]. The phosphorus (P) content of the dry mass of sewage sludge or sewage sludge ash ranges from a few to several percent [11, 12]. In poultry bones, P2O5 content is at a level of 18–20% [13]. Since the 1 of January 2016, recycling of phosphorus from sewage sludge and slaughter waste is mandatory requirement in Switzerland [14]. Germany and Austria are also preparing relevant regulations regarding the recycling process. Since Switzerland banned the direct application of sewage sludge onto the soil in 2006, its regulation has resulted in technical recovery and recycling in the form of inorganic products of phosphorus compounds [14].

The use of bones as a fertilizer dates back to biblical times [15]. In modern times, the management of slaughter waste in the form of bone meal, meat and bone meal and meal ashes to be used for fertilisation is a channel of phosphorus recovery that is an alternative to its use as feed. Meal ash, which used to be widespread, was first banned by the EU [16] (after the occurrence of BSE) and, later on, following the relaxation of relevant regulations, strongly limited [17]. Currently, meals are approved for use in agriculture as soil improvers, which, however, is also subject to numerous limitations aimed at ensuring that livestock have no contact with such preparations. Many authors indicate the good crop-enhancing efficiency of meat and bone meal [18, 19, 20] and meat and bone meal ash [21], compare to that of conventional fertilizers.

Management of sewage sludge is becoming a serious problem in the light of EU requirements regarding its storage. In Poland, a legal ban on the storage of sewage sludge containing more than 6% of organic mass has been in force since 2016 [22]. The direct use of sewage sludge for fertilisation purposes is allowed in Poland, provided that the acceptable levels of heavy metals and biogenic compounds are within the level [23]. The presence of harmful pathogens, as well as organic and inorganic contaminants, in sewage sludge prevents the incineration of their biomass [24]. Studies on usage of ashes originated from the incineration of sewage sludge as fertilizers have been carried out in many scientific centres [12, 25, 26, 27, 28]. The results of many of them are optimistic regarding the crop-enhancing efficiency in relation to various crop plants; however, a relationship with the technology of product manufacturing has also been observed [24, 25, 27].

A question that arouse is, whether fertilizers from wastes can either change or mitigate the European economy’s dependence on the major phosphorus suppliers [29].

Unprocessed phosphoric raw materials originating from both natural resources and secondary sources are characterised by low soluble compounds of phosphorous [10], which determine their limited fertilising efficiency due to poor solubility of the compounds. Solubility issues can be overcome by making use of phosphorus solubilizing microbes (PSMs), which transform phosphorus compounds from hardly available to bioavailable forms for plants consumption [30]. PSMs are abundantly found in agricultural soils. PSM also responsible for other direct and indirect biological mechanisms. They can act as plant-growth-promoting microorganisms (PGPMs) as well [30]. The properties of PSMs have been made use by using them as seed inoculants [31] or applying them along with phosphoric raw materials [32]. Recent research has shown that PSMs efficiently solubilise P from secondary raw materials as well [33].

Mineral fertilizers, particularly phosphorus fertilizers, are generally regarded as one of the major sources of heavy metals and other elements that have adverse effects on the environment [34]. On the other hand, they can affect the phytoavailability of heavy metals through modifying the properties of soil [34]. With a high content of readily soluble phosphates, hardly soluble cadmium phosphates and lead phosphates may precipitate in the soil.

The degree of heavy metal contamination of fertilizers is most largely affected by the raw material from which they are produced, and by the technological process used in their production [34, 35]. Phosphorus-containing rocks are naturally contaminated with heavy metals, yet the level of these elements changes depending on the source of the raw material [36, 37]. European markets primarily import phosphorites from North and East Africa and from the Middle East, which are characterised by relatively high cadmium content [36]. The tightening of the limits on Cd content to a value of 1 kg of P2O5, planned by the EU, has caused concern among fertilizer producers and farmers [37].

Heavy metals in soils may be a potential source of hazard to plants and groundwater [38]. The ability to take up and accumulate heavy metals, as well as tolerance to their presence in plant tissues, are genetic traits [39]. The uptake of trace elements from contaminated soils by plants often exceeds their physiological demand, which leads to phytotoxic effects [40]. After being incorporated into the trophic chain, they can contribute to maintaining the proper development of organisms in each of its links [38]. Significantly, heavy metals accumulate in the soil, and the consequences of soil contamination with those heavy metals, while being seldom visible in a short term, may lead to dangerous environmental changes in a long term [41]. An important characteristic that distinguishes heavy metals from other undesirable substances is that they are not biodegradable but only biotransformable, due to the complex physicochemical and biological processes occurring in the soil. These processes determine the mobility and bioavailability of heavy metals in the soil-plant system [34, 38, 41]. The uptake and accumulation of heavy metals in plants are determined by the soil properties, particularly its pH, granulometric composition and organic matter content [41]. Their mobility is also affected by the substances excreted by plant roots and soil microorganisms [42].

Bone waste contains no heavy metals [43], but these elements quite considerably restrict the use of sewage sludge ashes [26]. Many scientific centres are conducting studies on new technological solutions that can decrease the contents of toxic compounds in fertilizers which can be obtained from ashes and are within the acceptable level of heavy metals and other toxic elements [12, 24, 25, 26, 27]. In response to the need for phosphorus recycling, scientists from the Department of Advanced Material Technologies of the Wrocław Institute of Science and Technology have developed a technology of producing phosphorus biofertilizers from cheap renewable raw materials and PSM based on the previous studies on phosphorous solubilisation from secondary raw materials by the PSMs. It is expected that these innovative biofertilizers will not only be efficient in terms of crop-enhancing at a level comparable to conventional phosphorus fertilizers, but also ensure safety for consumers of field crops and for the environment. This study addresses the issue of the presence of cadmium and lead in the soil, crop plants, the accompanying weeds and post-harvest residues in the context of the application of biofertilizers originating from renewable raw materials. It was assumed that the biofertilizers would not elevate the level of these toxic elements in the soil and plant biomass compared with the commercial fertilizers, i.e. superphosphate.

2 Experimental procedures

2.1 Field experiments

In the years 2014-2016, four field experiments involving common wheat (Triticum aestivum ssp. vulgare Mac Key, winter or spring) were conducted, which tested five various biofertilizers produced on the basis of secondary raw materials, i.e. ash from the incineration of sewage sludge biomass from 3rd degree wastewater treatment and from poultry bones and phosphorus-solubilising bacteria of the Bacillus megaterium and Acidithiobacillus ferrooxidans strains (Table 1). The ash from sewage sludge was obtained from the municipal wastewater treatment plant ‘Łyna’ in Olsztyn and the bones from households or from the Firma Handlowo-Produkcyjna ‘Podolski’ (with registered office in Lutome, Wielkopolskie Voivodeship, Poland). The bacteria strains were obtained from the Polish Collection of Microorganisms at the Institute of Immunology and Experimental Therapy of the Polish Academy of Sciences in Wrocław (Poland). Phosphorus solubilisation involving Bacillus megaterium occurs due to the production of weak organic acids (citric, propionic) [10]. In the presence of sulphur, Acidithiobacillus ferrooxidans produce sulphuric acid, thus increasing the intensity of the digestion of the phosphorus raw material [10]. The procedure of obtaining fertilizer formulations were described elsewhere [44, 45]. The elemental composition of biofertilizers is provided in the Table 2.

Table 1

Biofertilizers tested in the experiments.

Table 2

Elemental composition of biofertilizers.

Biofertilizers were tested and compared with no phosphorus fertilisation (No P – no phosphorus fertilization – a control object in each experiment) and superphosphate Fosdar™ 40 (SP). This all-purpose phosphorus fertilizer contains 40% P2O5, 10% CaO, 5% SO3, and microelements (B, Co, Cu, Fe, Mn, Mo, and Zn) according to the commercial information provided on the label.

In experiment I, phosphorus fertilizers were applied to the wheat crop at a P2O5 dose of 48 kg ha−1, and in experiments II-IV, the P2O5 doses were applied at 3 different levels: 40, 60, and 80 kg ha−1. Fertilizer suspensions were applied by coarse droplet spraying and solid fertilizers were sown. In experiment I, the plants were not protected against pests (−PP), in experiment II, two variants of plant protection were adopted: without the protection (−PP) and with full protection (+PP), and in experiments III and IV, full protection (+PP) was applied.

Wheat was cultivated annually in a soil adjusted to its species requirements (Table 3). Cd and Pb contents of the soil before the start of each experiment fell within a range considered to be natural, and did not exceed the acceptable standards for agricultural use (Table 4). Basic agricultural data for the experiments are provided in Table 5. The precipitation and thermal conditions during the growing seasons were different from the values typical of the region and were not favourable to the cultivated plants (Table 6). In experiments I-III, the growing seasons for spring and winter wheat proved to be very dry, while in experiment IV, winter wheat developed under wet season conditions. The water content of the soil may change the availability of metals to plants [54]. Heavy precipitation may also result in the rain-out of metals from the surface layers of the soil and in their accumulation in the depressions of the ground [55].

Table 3

Soil characteristic before the start of the experiments.

Table 4

Reference values for cadmium and lead contents (mg kg–1) of the soil and plants, according to various sources.

Table 5

Basic agricultural data for the experiments.

Table 6

Precipitations and air temperatures during the period of study according to the Meteorological Station in Bałcyny.

Experiments I, III, and IV were established in a randomised block design and experiment II in a parallel strip design. In each experiment, particular experimental variants were performed in 4 replications.

2.2 Soil and plant sampling

The soil was sampled using a core soil sampler from the 0-30 cm layer from each plot from evenly spaced points. A total of approx. 1 kg of soil was collected from an individual plot. The soil was dried at room temperature for several days, thoroughly mixed and sieved, and then separated into portions of approx. 300 g which were subjected to chemical analyses.

The mass of grains obtained during the combine harvesting from each plot was thoroughly mixed and samples weighing approx. 1 kg were taken. From each sample, approx. 200 g of grains were weighed, cleaned to get rid of impurities and weed seeds and then subjected to chemical analyses.

Just before the harvesting of wheat, plants were collected manually from two 1-metre-long rows of each plot and the spikes and roots were then cut off at a height corresponding to the height of mowing by a combine harvester. Straw (i.e. stems with leaves) was cut into pieces of approx. 10 cm in length. The samples were dried at room temperature for several days, and then a portion of 50 g was weighed from each sample and subjected to chemical analyses.

Weeds were sampled from a randomly determined area of 0.25 m2 (0.5 m × 0.5 m frame) from each plot prior to harvesting the test plant. After the separation of the roots, the above-ground biomass of weeds was dried at room temperature for several days and the samples in their entirety (different mass) were then forwarded for chemical analyses.

Post-harvest residues were sampled from an area of 0.40 m2 and from a depth of 0.30 m. After washing the collected mass on sieves and removing earthy portions, the roots, stubble and weed residues were separated and dried at room temperature for several days and were then forwarded for chemical analyses.

2.3 Analyses

The Cd and Pb contents of the soil and plant material were determined using a inductively coupled plasma-optical emission spectrometer (ICP-OES). The appropriate mass (0.5 g) of biological sample materials (plant and soil samples) was digested in Teflon vessels (microwave oven Milestone MLS-1200) with 5 mL of concentrated 65 mg kg−1 HNO3 suprapur grade from Merck in the case of plant samples, and with 10 mL of aqua regia in the case of soil samples. After mineralization, all samples were diluted to 50 mL. The ICP-OES with an pneumatic nebulizer with axial view (iCAP Duo Thermo Scientific, USA) was used to determine the concentration of elements in all digested and diluted biological samples. Determination of content of toxic metal ions was carried out with all the principles of measurement traceability. Determination of content of toxic metal ions was carried out with all the principles of measurement traceability. What is more, certificated reference materials were used to check the quality and metrological traceability. The detection levels for Cd and Pb for the soil material were 0.01 and 0.15 mg kg−1, respectively, and for the plant material they were 0.001 and 0.01 mg kg−1, respectively.

2.4 Calculations

The results were processed using an analysis of variance, or the alternative Kruskal-Wallis test if the analysis of variance assumptions were not met. The normality of variable distribution was checked using the Shapiro–Wilk W-test and the homogeneity of variance was checked using Levene’s test. The differences between objects were evaluated using Duncan’s test or a multiple comparison test. In statistical calculations, the samples with element contents above the detection level (LD) were replaced by values equal to the LD. For each experiment, the median and the maximum value were determined. The relationships between the analysed variables were expressed using simple correlation coefficients determined based on the data from all experiments. In all cases, p=0.05 was assumed. The calculations were performed using Statistica 12.0 software.

Ethical approval

The conducted research is not related to either human or animals use.

3 Results and Discussion

3.1 Cadmium (Cd)

The Cd content of the soil in the experiments (Table 7) fell within the range regarded as natural under Polish conditions and did not exceed allowable levels for arable land (Table 4). The average values in the experiments did not differ from the average national and regional values and even the highest values determined (0.642 mg kg−1 in 2016) fell within the range of the geochemical background (Tables 4 and 7).

Table 7

Cadmium content in soil and plant biomass from wheat field, mg kg–1 (dry matter).

No effect of the fertilisation factor on the Cd content of the topsoil layer was found in any of the experiments (Table 7). Biofertilizers from renewable raw materials, similar to superphosphate, irrespective of the P2O5 dose, did not significantly change the content of this element as compared to the control. In experiments I and IV, no significant change occurred in relation to the baseline state of the soil (prior to the start of the experiments) and in experiments II and III, the level of Cd in the soil in relation to the baseline state decreased with no relation to the phosphorus fertilisation applied. The application of the protection of plants in comparison with the lack of plant protection treatments (experiment II) did not change the Cd content of the soil either. The medians in the experiments were usually at a level below the detection level (an exception was experiment IV).

Previous studies indicated that feeding the plants with either mineral or organic fertilizers of primary or secondary origin, which are rich in Cd, may result in a significant increase in the content of this element in the soil [56, 57], even during one growing season [56] and contribute to an increase in its more or less intense uptake and accumulation in plants [57, 58, 59, 60]. Many reports have been published, according to which the secondary sources of nutrients, such as hard coal ash [60], sewage sludge and a mixture with brown coal and ashes [61], sheep manure compost [62], poultry manure [63], did not contribute to increase the Cd content of the soil [61, 62, 63] or of the crop plant growing on this soil [60, 62, 63].

Wierzbowska et al. [64], while using ash from the incineration of sewage sludge (wastewater treatment plant Łyna, Olsztyn) as a phosphorus fertilizer in the cultivation of Virgina fanpetals, noted no differences in its effect on the Cd content of the soil, but the Cd content of plants increased.

In our experiments, the applied biofertilizers (similar to superphosphate) irrespective of the dose of the pure component, did not significantly change the Cd content of wheat grains or straw, in the accompanying weeds or in post-harvest residues.

In the plant material, Cd was usually present in amounts regarded as natural, and none of the experiments approached a level indicating an excessive or toxic content of Cd (Tables 4 and 7).

In the grains, Cd was usually present in amounts far below the acceptability threshold for wheat, which is indicated not only by the low median values but also by the maximum values noted in experiments II-IV. The relatively highest amounts of Cd in the grains were determined in 2014 (experiment I); however, even in this case, the maximum value (0.138 mg kg−1) was below the acceptability threshold.

Greater contents of Cd were usually found in wheat straw than in the grains, which is consistent with the conclusions of previously reported studies [65, 66]. An exception was observed in experiment I in which the content of Cd in the straw was lower than that in the grains. This may be due to the relatively low Cd content of the soil and the highest pH value of the soil. It is known that under conditions of a higher pH value, the uptake of Cd by plants is blocked [34, 67]. This hypothesis was also confirmed by the fact that the relatively lowest Cd content of the weed biomass was observed in experiment I. The relatively highest Cd content of the straw was determined in experiment II. This level, however, does not disqualify it as a feed stuff (Table 4). A higher content in straw could have been associated with the more intense uptake of this element by plants on the soil with a lower pH value (in relation to experiment I). In this experiment, a higher Cd content as compared to that in experiment I was also observed in the weeds.

Plant protection against pests (experiment II) had no effect on the Cd content of wheat grains and straw. Similarly, Wołejko et al. [42] found protection treatments with fungicide and herbicide conducted during the growing season did not result in exceeding the significant concentration of Cd in grain or leaves of wheat growing on soil enriched with granular sludge.

The Cd content of weeds in experiment II was differentiated by the protection of plants; specifically, its effect on the species structure of the weeds. In the biomass of weeds from the unprotected wheat field, Chenopodium album and Fallopia convolvulus, which accumulated more Cd than other species, were predominant (unpublished data). The limitation of their share in the community thanks to the herbicide (protected wheat field) contributed to a decrease in the Cd content of the overall mass of weeds and was manifested by a significant difference in relation to the un-weeded wheat fields. The ability of these species to accumulate Cd was also documented by Stupnicka-Rodzynkiewicz et al. [68, 69], who also indicated the differentiation of the Cd content depending on the soil properties. Relatively high Cd contents of the weeds were observed in experiment III: the average values and the median exceeded 1 mg kg−1, and the maximum value amounted to 2.606 mg kg−1. In the community concerned, the predominant species was Viola arvensis, which proved to be quite resistant to the applied herbicide and accumulated large amounts of Cd in its mass. It appears probable that the accumulation of Cd by the weeds restricted the uptake and accumulation of Cd in wheat plants [70]. Violaceae exhibit high tolerance to heavy metals [71]; the significant ability of Viola arvensis to accumulate Cd was reported by Stupnicka-Rodzynkiewicz et al. [68, 69].

The Cd content of post-harvest residues was at a similar level in experiments I and II, and slightly elevated in experiment III. The level of Cd in their mass is determined by the ratio between the residues of the roots, stubble and weeds. Cd has a high bioaccumulation coefficient [42], is relatively intensely taken up by plants and is easily transported by the root system to all organs, but usually the roots of cereals accumulate more Cd than the stubble [72, 73], which was confirmed by our own study. In turn, the accumulation in weed residues depends on the weed species being part of the mass of post-harvest residues as well as of their organs [74]. The percentage of V. arvensis in post-harvest residues in experiment III appears to be responsible for the slightly elevated Cd level in their overall biomass.

The Cd content of the soil demonstrated no significant relationship with its accumulation in plants (Table 9), while an increase in Cd accumulated in weeds and postharvest residues resulted in less of it being found in wheat grains and straw. However, the Cd contents of weeds and post-harvest residues were convergent. Ociepa et al. [61], concluded that the heavy metal content of the above-ground parts of prairie cordgrass (Spartina pectinata) were not dependent on the total metal content of the soil. Hirzel et al. [73] reported that Cd accumulation in grains, straw, and roots of durum wheat was significantly affected by increasing Cd rates, and Wang et al. [75] reported that Cd content of wheat grains was positively correlated with its content in the roots. In a study by Rogóż [74], the Cd content of plants of certain weed species exhibited dependence on the content of this element in the soil and decreased with an increase in the pH value above 5.5.

Table 8

Lead content in soil and plant biomass from wheat field, mg kg–1 (dry matter).

Table 9

Simple correlation coefficients calculated between the cadmium and lead content in soil and plant biomass.

3.2 Lead (Pb)

In the experiments, Pb (similarly to Cd) was found in soils (Table 8) in concentration regarded as natural in Poland and did not exceed levels acceptable for agricultural use (Table 4). Referring to the geochemical background for Poland, the Pb content of soils under experimental conditions must be regarded as low. Only the maximum values determined in particular experiments (the highest value of 14.484 mg kg−1 in 2014) were at a level of national (average and median) and regional statistics (Table 4).

In none of the experiments the variants of phosphorus fertilisation changed the Pb content of the topsoil layer; the use of phosphorus in relation to the omission of fertilisation or the type and dose of fertilizer did not differentiate this characteristic (Table 8). In experiment I, only a trend toward increasing the Pb content of the soil after the application of superphosphate and biofertilizers from ash and bones was observed, but no statistical confirmation given and, considering the context of results of the remaining experiments, this should not raise concerns.

Similar to Cd, no significant change occurred in experiments I and IV in relation to the baseline state of the soil (prior to the start of the experiments) and in experiments II and III, the level of Pb in the soil in relation to the baseline state decreased with no relation to the phosphorus fertilisation applied. The protection of plants in comparison with the absence (experiment II) also did not change the Pb content of the soil.

Atafar et al. [56] reported a dramatic increase in Pb content of the soil during the growing season (from the state before fertilisation to the state after harvesting the crop plant) under the influence of mineral fertilizers rich in Pb. Numerous authors have also noted an increase in the total content of Pb or its forms in the soil as a result of the use of fertilizers from secondary sources [57, 62, 76, 77]; however, opinions on the lack of effect of fertilizers on the level of Pb in soil have also been raised [63, 64]. Moreover, results of studies into the effects of fertilizers on Pb content of plants also provide divergent information [57, 60, 62, 63, 78, 79].

It follows from the studies carried out so far that the uptake of Pb from the soil by plant roots is low, but its bioavailability to plants can be changed due to a change in the pH value, organic compound content, iron oxides and the amount of phosphorus which has an antagonistic effect on the uptake of Pb [67]. Guo et al. [72] decreased, even in contaminated soil, the content of available forms of Cd and Pb as well as the content of these elements in wheat grains through the use of phosphorus fertilizers (sepiolite, single superphosphate, triple super phosphate, calcium magnesium phosphate). In general, the cultivation of plants on soils whose Pb content does not exceed 300 mg kg−1 is regarded as safe [38].

In our study, biofertilizers from secondary raw materials (just like superphosphate) irrespective of the dose of a pure component, did not significantly change the Pb contents of wheat grains or straw, the weeds growing in a corn field or in the post-harvest plant residues in any of the experiments (Table 8).

In the tested plant biomass, Pb was usually found in concentration accepted as natural, satisfactory or normal. The contents were far from levels regarded as excessive or toxic to plants in all of the experiments (Table 4).

In the grains, Pb was usually found in small amounts far from the acceptability threshold (Table 4), which is demonstrated by the values of medians in the experiments (incidentally, higher contents approaching the threshold value were also determined in experiments II and III).

This should not, however, raise concerns since as elevated values were also noted in control samples and they should be considered in terms of an experimental error.

The protection of plants in comparison with an absence (experiment II) did not change the Pb content of wheat grains. Wołejko et al. [42] reported that the concentration of Pb in wheat grain protected by MCPA and 2,4-D with thiophanate-methyl and azoxystrobin was higher than the maximum levels of 0.20 mg kg−1 D.M.

Generally, in our study, Pb accumulated in greater amounts in wheat straw than in its grains, which is consistent with other reports [38]. The relatively highest level of Pb content of the straw was noted in experiment II. Significantly, the average values were approx. 10-fold higher than those in straw from the other experiments (exceeding 1 mg kg−1) and the maximum content was determined to be 5.520 mg kg−1. This content does not exceed the level of acceptable content in feed materials of plant origin (Table 4). This could be associated with the pH value of the soil, since in more acidic soils the uptake of this element by plants increases [38]. In experiment III (a similar pH level), the Pb content of post-harvest residues suggests that the metal was retained in the roots to a greater extent than it was retained in straw. In experiment IV, the uptake and distribution of Pb in plants could have been determined by the relatively lowest Pb content of the soil. In experiment II, the protection of plants in comparison with the absence of protection did not change the straw Pb content.

The overall Pb content of the weed biomass in particular experiments was primarily determined by the species structure of the community and by the species’ suitability for the accumulation of this element. This is particularly evident in experiment II in which the protection of plants, while reducing the percentage of dominant weed species (Chenopodium album and Fallopia convolvulus) accumulating smaller amounts of Pb (unlike for Cd), contributed to an increase in the Pb content of the weed mass due to increasing the proportion of other species accumulating greater amounts of Pb. Viola arvensis (primarily in experiment III) proved to be a poorer accumulator of Pb than of Cd, which supports the results of Stupnicka-Rodzynkiewicz et al. [68].

The mobility of Pb in plants is very much limited and most of this element is accumulated in the roots [38, 57, 67], hence the Pb content of post-harvest residues was mainly determined by the percentage of Pb within the entire mass as well as by its percentage and the species structure of the weed remnants. In experiment II, a higher percentage of weeds in the mass of residues from the unprotected wheat field determined the reduction in Pb content of these residues in relation to the residues originating from the weeded wheat field, in whose residues the roots had a relatively higher percentage.

The lead content of the soil demonstrated an inverse correlation with the content in straw and in the weeds, with no relation to the grains and residues (Table 9). Other studies confirm that the seeds are the organs which are most protected by plants against the excessive accumulation of toxic elements [38].

Findings in our study are in alignment with the conclusion drawn by previously reported studies [80, 81] that explains the reasonable use of fertilizers from renewable raw materials, with low toxic element contents, are not considered to pose a hazard to the soil or to food chains.

4 Conclusion

Phosphorus biofertilizers from sewage sludge ash and from bones, microbiologically activated and applied in amounts of P2O5 up to 80 kg ha−1, did not change the Cd and Pb contents of the soil, grain or straw of the tested plants, or the mass of accompanying weeds or of post-harvest residues, similar to superphosphate. Both Cd and Pb in the soil and plant biomass occurred in amounts regarded as natural and are within the acceptable standards.

Reasonably applied biofertilizers from renewable raw materials, with low toxic element contents, are not believed to pose a hazard to the soil or plants and may be used as a substitute for conventional, phosphorite-based fertilizers.

Acknowledgements

This research is financed in the framework of grant PBS 2/A1/11/2013, ‘Phosphorus renewable raw materials – a resource base for new generation of fertilizers’ attributed to the National Center for Research and Development of Poland.

References

  • [1]

    Sultenfuss J.H., Doyle W.J., Functions of phosphorus in plants. Better Crops, 1999, 83(1), 6-7. Google Scholar

  • [2]

    Schröder J.J., Cordell D., Smit A.L., Rosemarin A., Sustainable use of phosphorus, Technical Report Report 357 for Plant Research International, Wageningen University and Research Centre, Wageningen, The Netherlands, 2010. Google Scholar

  • [3]

    Mineral commodity summaries 2017. Phosphate rock. U.S.G.S. 2017. Google Scholar

  • [4]

    Korzeniowska J., Stanisławska-Glubiak E., New trends in using rock phosphates in agriculture, Post. Nauk Rol., 2011, 3, 57-66, (in Polish). Google Scholar

  • [5]

    Report on critical raw materials for the EU. Report of the Ad hoc Working Group on defining critical raw materials, May 2014. European Commission, 2014. Google Scholar

  • [6]

    Tenkorang F., Lowenberg-DeBoer J., Forecasting long-term global fertilizer demand. Nutr. Cycl. Agroecosys., 2009, 83, 233-247. CrossrefGoogle Scholar

  • [7]

    Waste Atlas – Interactive map with visualized waste management data, Global Waste Clock, http://www.atlas.d-waste.com/ 

  • [8]

    Jaskulski D., Jaskulska I., Possibility of using the waste from the production process of polyvinyl chloride to product generating for plant fertilization, Pol. J. Environ. Stud., 2011, 20(2), 351-354. Google Scholar

  • [9]

    Romiński M., Michalak P., Jaskulski D., Jaskulska I., Technology for manufacturing granulated magnesium fertilizers with the use of wastes from chlorine production. Przem. Chem., 2011, 90(4), 628-630, (in Polish). Google Scholar

  • [10]

    Saeid A., Labuda M., Chojnacka K., Górecki H., Use of microorganism in production of phosphorus fertilizers, Przem. Chem., 2012, 91(5), 956-958, (in Polish). Google Scholar

  • [11]

    Poluszyńska J., Ślęzak E., Phosphorus from municipal sewage sludge, Scientific Works of Institute of Ceramics and Building Materials, 2015, 22, 44-55, (in Polish). Google Scholar

  • [12]

    Smol M., Kulczycka J., Kowalski Z., Sewage sludge ash (SSA) from large and small incineration plants as a potential source of phosphorus - Polish case study, J. Environ. Manage., 2016, 184, 617-628. CrossrefPubMedGoogle Scholar

  • [13]

    Wyciszkiewicz M., Saeid A., Samoraj M., Chojnacka K., Solid-state solubilization of bones by B. megaterium in spent mushroom substrate as a medium for a phosphate enriched substrate, J. Chem. Technol. Biotechnol., 2017, 92, 1397-1405. CrossrefGoogle Scholar

  • [14]

    European Sustainable Phosphorus Platform, Scope and News. Switzerland makes phosphorus recycling obligatory, Published: 07 December 2015. Google Scholar

  • [15]

    Wisniak J., Phosphorus – from discovery to commodity, Indian J. Chem. Techn., 2005, 12, 108-122. Google Scholar

  • [16]

    Regulation (EC) No 999/2001 of the European Parliament and of the Council of 22 May 2001 laying down rules for the prevention, control and eradication of certain transmissible spongiform encephalopathies, Official Journal L 147, 31/05/2001 P. 0001 – 0040. Google Scholar

  • [17]

    Commission Regulation (EU) No 142/2011 of 25 February 2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive. Official Journal of the European Union L 54, 26.2.2011. Google Scholar

  • [18]

    Jeng A.S., Haraldsen T.K., Grønlund A., Pedersen P.A., Meat and bone meal as nitrogen and phosphorus fertilizer to cereals and ryegrass, Nutr. Cycl. Agroecosys., 2006,76(2-3), 183-192. Google Scholar

  • [19]

    Stępień A., The effect of meat and bone meal on soil properties and crop yield, Dissertations and Monographs, 2011, 161, 1-110, (in Polish). Google Scholar

  • [20]

    Nogalska A., Chen L., Sienkiewicz S., Nogalski Z., Meat and bone meal as nitrogen and phosphorus supplier to cereals and oilseed rape, Agr. Food Sci., 2014, 23(1), 19-27. CrossrefGoogle Scholar

  • [21]

    Alotaibi K.D., Schoenau J.J., Fonstad T., Possible utilization of ash from meat and bone meal and dried distillers grains gasification as a phosphorus fertilizer: crop growth response and changes in soil chemical properties, J. Soil Sediment, 2013, 13(6), 1024-1031. CrossrefGoogle Scholar

  • [22]

    Ordinance by the Minister of Economy (Poland) of 8 January 2013 on the criteria and procedures for the acceptance of waste for landfilling of given waste type, Journal of Laws of the Republic of Poland of 2013, item 38, (in Polish). Google Scholar

  • [23]

    Ordinance by the Minister of the Environment (Poland) of 13 July 2010 on municipal sewage sludge, Journal of Laws of the Republic of Poland of 2010, No 137, item 813, (in Polish). Google Scholar

  • [24]

    Severin M., Breuer J., Rex M., Stemann J., Adam Ch., Van den Weghe H., Kücke M., Phosphate fertilizer value of heat treated sewage sludge ash, Plant Soil Environ., 2014, 60(12), 555-561. CrossrefGoogle Scholar

  • [25]

    Weigand H., Bertau M., Hübner W., Bohndick F., Bruckert A., RecoPhos: Full-scale fertilizer production from sewage sludge ash, Waste Manage., 2013, 33(3), 540-544. CrossrefGoogle Scholar

  • [26]

    Herzel H., Krüger O., Hermann L., Adam C., Sewage sludge ash – a promising secondary phosphorus source for fertilizer production, Sci. Total Environ., 2016, 542, 1136-1143. CrossrefGoogle Scholar

  • [27]

    Lekfeldt J.D.S., Rex M., Mercl F., Kulhánek M., Tlustoš P., Magid J., de Neergaard A., Effect of bioeffectors and recycled P-fertiliser products on the growth of spring wheat. Chem. Biol. Techn. Agric., 2016, 3, 22. CrossrefGoogle Scholar

  • [28]

    Gorazda K., Tarko B., Wzorek Z., Kominko H., Nowak A.K., Kulczycka J., Henclik A., Smol M., Fertilisers production from ashes after sewage sludge combustion - A strategy towards sustainable development, Environ. Res., 2017, 154, 171-180. PubMedCrossrefGoogle Scholar

  • [29]

    Konieczka P., Cieslik B.M., A review of phosphorus recovery methods at various steps of wastewater treatment and sewage sludge management. The concept of “no solid waste generation” and analytical methods, J. Clean. Prod., 2017, 142, 1728-1740. CrossrefGoogle Scholar

  • [30]

    Karpagam T., Nagalakshmi P.K., Isolation and characterization of phosphate solubilizing microbes from agricultural soil, Int. J. Curr. Microbiol. App. Sci., 2014, 3(3), 601-614. Google Scholar

  • [31]

    Ram H., Malik S.S., Dhaliwal S.S., Kumar B., Singh Y., Growth and productivity of wheat affected by phosphorus-solubilizing fungi and phosphorus levels. Plant Soil Environ., 2015, 61(3), 122-126. Google Scholar

  • [32]

    Stella M., Syahren A.M., Application of phosphate solubilising microorganisms to increase the solubilisation of rock phosphates in soil, J. Trop. Agric. and Fd. Sc., 2016, 44(1), 9-18. Google Scholar

  • [33]

    Wyciszkiewicz M., Saeid A., Dobrowolska-Iwanek J., Chojnacka K., Utilization of microorganisms in the solubilization of low-quality phosphorus raw material, Ecol. Eng., 2016, 89, 109-113. CrossrefGoogle Scholar

  • [34]

    Sady W., Smoleń S., Influence factors soil-fertilizer the accumulation of heavy metals in plants, In: Proceedings of X National Symposium ‘Effectiveness of the use of fertilizers the horticultural crops’ (17-18 June 2004, Kraków, Poland), Wydawnictwo Akademii Rolniczej w Poznaniu, Poznan, 2004, 269-277, (in Polish). Google Scholar

  • [35]

    Gambuś F., Wieczorek J., Polution of fertilizers with heavy metals, Ecol. Chem. Eng., 2012, 19(4-5), 353-360, (in Polish). Google Scholar

  • [36]

    Mar S.S., Okazaki M., Investigation of Cd contents in several phosphate rocks used for the production of fertilizer, Microchem. J., 2012, 104, 17-21. CrossrefGoogle Scholar

  • [37]

    Cichy B., Jaroszek H., Paszek A., Cadmium in phosphate fertilizers; ecological and economical aspects, Chemik, 2014, 68(10, 837-842. Google Scholar

  • [38]

    Wuana R.A., Okieimen F.E., Heavy metals in contaminated soils: a review of sources, chemistry, risks and best available strategies for remediation, Int. Sch. Res. Net. Ecol., 2011, 1-20. Google Scholar

  • [39]

    Gambuś F., Heavy metal uptake by various agricultural crops. P. 1. Plant sensitivity to heavy metals. Acta Agr. Silv., Ser. Agr., 1997, 35, 21-29, (in Polish). Google Scholar

  • [40]

    Niesiobędzka K., Mobile forms and migration ability of Cu, Pb and Zn in forestry system in Poland, Environ. Earth Sci., 2016, 75:122. Google Scholar

  • [41]

    Czech T., Baran A., Wieczorek J., Content of heavy metals in soil and plants from area Borzęcin municipality (Małopolska province). Inż. Ekol., 2014, 37, 89-98, (in Polish). Google Scholar

  • [42]

    Wołejko E., Łozowicka B., KaczyŃski P., Konecki R., Grobela M., The influence of chemical protection on the content of heavy metals in wheat (Triticum aestivum L.) growing on the soil enriched with granular sludge, Environ. Monit. Assess., 2017, 189: 424. PubMedCrossrefGoogle Scholar

  • [43]

    StaroŃ A., Kowalski Z., Banach M., Wzorek Z., Methods of thermal utilization of animals wastes, Chem. Trans. Chem., 2010, 1, 323-332, (in Polish). Google Scholar

  • [44]

    Rolewicz M., Rusek P., Borowik K., Obtaining of granular fertilizers based on ashes from combustion of waste residues and ground bones using phosphorous solubilization by bacteria Bacillus megaterium, J. Environ. Manage., 2017, https://doi.org/10.1016/j.jenvman.2017.05.004, in press. PubMed

  • [45]

    Rolewicz M., Rusek P., Mikos-Szymanska M., Cichy B., Dawidowicz M., Obtaining of suspension fertilizers from incinerated sewage sludge ashes (ISSA) by a method of solubilization of phosphorus compounds by Bacillus megaterium bacteria, Waste Biomass Valori., 2016, 7(4), 871-877. CrossrefGoogle Scholar

  • [46]

    Markert B., Presence and significance of naturally occurring chemical elements of the periodic system in the plant organism and consequences for future investigations on inorganic environmental chemistry in ecosystems, Vegetatio, 1992, 103, 1-30. Google Scholar

  • [47]

    Czarnowska K., Total content of heavy metals in parent rocks as reference background levels of soils, Rocz. Gleb., 1996, 47, 43-50, (in Polish). Google Scholar

  • [48]

    Kabata-Pendias A., Pendias H., Biogeochemistry of Trace Elements, 2nd ed., PWN Warszawa, 1999. Google Scholar

  • [49]

    Ordinance by the Minister of the Environment (Poland) of 1 September 2016 on assessment procedures for the land surface pollution. Journal of Laws of the Republic of Poland of 2016, item 1395, (in Polish). Google Scholar

  • [50]

    The monitoring of the chemistry of Polish arable soils in 2015. Institute of Soil Science and Plant Cultivation (IUNG), Puławy, Poland, 2015, http://www.gios.gov.pl/chemizm_gleb/ 

  • [51]

    Kabata-Pendias A., Trace elements in soils and plants, 4th ed., CRC Press Taylor and Francis Group, Boca Raton, 2011. Google Scholar

  • [52]

    Ordinance by the Minister of Health (Poland) of 13 January 2003 on maximum concentrations of chemical and biological impurities which may be present in food, food ingredients, permitted supplemetary substances and substances helpful in food processing. Journal of Laws of the Republic of Poland of 2003, No 37, item 326, (in Polish). Google Scholar

  • [53]

    Ordinance by the Minister of Agriculture and Rural Development (Poland) of 25 August 2014 amending the ordinance on the content of undesirable substances in animal feed. Journal of Laws of the Republic of Poland of 2014, No 37, item 1213, (in Polish). Google Scholar

  • [54]

    Wiśniowska-Kielian B., Effect of soil moisture content on the absorption of heavy metals by plants. Zesz. Probl. Post. Nauk Roln., 2000, 471, 587-595, (in Polish). Google Scholar

  • [55]

    Gancarczyk-Gola M., Palowski B., Heavy metals and acidity of surface soil horizons in surroundings of industrial centers and in non-contaminated regions, Rocz. Gleb., 2005, 56(1/2), 59-66, (in Polish). Google Scholar

  • [56]

    Atafar Z., Mesdaghinia A., Nouri J., Homaee M., Yunesian M., Ahmadimoghaddam M., Mahvi A.H., Effect of fertilizer application on soil heavy metal concentration, Environ. Monit. Assess., 2010, 160(1-4), 83-89. PubMedCrossrefGoogle Scholar

  • [57]

    Belhaj D., Elloumi N., Jerbi B., Zouari M., Abdallah F.B., Ayadi H., Kallel M., Effects of sewage sludge fertilizer on heavy metal accumulation and consequent responses of sunflower (Helianthus annuus), Environ. Sci. Pollut. Res., 2016, 23, 20168-20177. CrossrefGoogle Scholar

  • [58]

    Gondek K., Effect of mineral fertilisation, farmyard manure and tannery sludge treatment on selected heavy metal concentrations in plants and soil, Acta Agrophys., 2004, 3(3), 465-478, (in Polish). Google Scholar

  • [59]

    Wong J.W.C, Selvam A., Growth and elemental accumulation of plants grown in acidic soil amended with coal fly ash-sewage sludge compost, Environ. Contam. Toxicol., 2009, 57, 515-523. CrossrefGoogle Scholar

  • [60]

    Godlewska A., Changes in the contents of selected heavy metals in test plants fertilised with sewage sludge and hard coal ash, J. Ecol. Eng., 2017, 18(2), 97-102. CrossrefGoogle Scholar

  • [61]

    Ociepa E., Pachura P., Ociepa-Kubicka A., Effect of fertilization unconventional migration of heavy metals in the soil-plant system, Inż. Ochr. Śr., 2014, 17(2), 325-338, (in Polish). Google Scholar

  • [62]

    Wang F., Wang Z., Kou C., Ma Z., Zhao D., Responses of wheat yield, macro- and micro-nutrients, and heavy metals in soil and wheat following the application of manure compost on the North China Plain. PLoS ONE, 2016, 11(1), e0146453.  CrossrefPubMedGoogle Scholar

  • [63]

    Delgado Arroyo M.M., Mirralles De Imperial Hornedo R., Alonso Peralta F., Rodriguez Almestre C., Martinez Sanchez J.V., Heavy metals concentration in soil, plant earthworm and leachate from poultry manure applied to agricultural land, Rev. Int. Contam. Ambie., 2014, 30(1), 43-50. Google Scholar

  • [64]

    Wierzbowska J., Sienkiewicz S., Sternik P., Busse M.K., Using ash from incineration of municipal sewage sludge to fertilize Virginia fanpetals, Ecol. Chem. Eng., 2015, 22(4), 497-507. Google Scholar

  • [65]

    Andruszczak E., Strqczynski S., Czerniawska W., Radwan B., Content of some elements in soils and plants as influenced by emissions of the copperworks, Rocz. Gleb., 1986, 37(4), 47-66, (in Polish). Google Scholar

  • [66]

    Kaszubkiewicz J., Kawałko D., Total content of heavy metals in soils and plants et the area of Jelenia Góra district. Ochr. Śr. Zasobów Nat., 2009, 40, 177-189, (in Polish). Google Scholar

  • [67]

    Ociepa-Kubicka A., Ociepa E., Toxic effects of heavy metals on plants, animals and humans. Inz. Ochr. Sr., 2012, 15(2),169-180, (in Polish). Google Scholar

  • [68]

    Stupnicka-Rodzynkiewicz E., Łabza T., Hochół T., Content of some mineral components in weeds with respect to environmental conditions. Acta Agr. Silv., Ser. Agr., 1996, 34, 125-130. Google Scholar

  • [69]

    Stupnicka-Rodzynkiewicz E., Hochół T., Łabza T., Content of cadmium in selected segetal weeds. Zesz. Probl. Post. Nauk Rol., 1997, 448b, 303-307, (in Polish). Google Scholar

  • [70]

    Ashrafi A., Zahedi M., Fahmi K., Nadi R., Neighbour effects of purslane (Portulaca oleracea L.) on Cd bioaccumulation by soybean in saline soil, Plant Soil Environ, 2014, 60(10), 439-445. CrossrefGoogle Scholar

  • [71]

    Słomka A., Sutkowska A., Szczepaniak M., Malec P., Mitka J., Kuta E., Increased genetic diversity of Viola tricolor L. (Violaceae) in metal-polluted environments, Chemosphere, 2011, 83(4), 435-442. CrossrefPubMedGoogle Scholar

  • [72]

    Guo G., Lei M., Chen T., Yang J., Evaluation of different amendments and foliar fertilizer for immobilization of heavy metals in contaminated soils, J. Soils Sediments, 2017, https://doi.org/10.1007/s11368-017-1752-y

  • [73]

    Hirzel J., Retamal-Salgado J., Walter I., Matus I., Cadmium accumulation and distribution in plants of three durum wheat cultivars under different agricultural environments in Chile, J. Soil Water Conserv., 2017, 72(1), 77-88. CrossrefGoogle Scholar

  • [74]

    Rogóż A., Trace elements content in cereal weeds against the background of their soil contents. Part 3. Cadmium and nickel contents in soil and weeds, Ecol .Chem. Eng. A., 2012, 19(9),1063-1071. Google Scholar

  • [75]

    Wang X.R., Zhou S.L., Wu S.H., Accumulation of heavy metals in different parts of wheat plant from the Yangtze River delta, China, Int. J. Agric. Biol., 2016, 18, 1242-1248. CrossrefGoogle Scholar

  • [76]

    Gu C., Bai Y., Tao T., Chen G., Shan Y., Effect of sewage sludge amendment on heavy metal uptake and yield of ryegrass seedling in a mudflat soil, J. Environ. Qual., 2013 42(2), 421-428. CrossrefGoogle Scholar

  • [77]

    Antonkiewicz J., Kowalewska A., Pełka R., Content of heavy metals and their fractions in soil in result of residual effect of waste materials, Ecol. Chem. Eng. A, 2014, 21(4), 439-452. Google Scholar

  • [78]

    Antonkiewicz J., Effect of ash-and-sludge and ash-and-peat blends on field of Grass-birds-foot trefoil mixture and level of selected elements in mixture, Acta Sci. Pol., Formatio Circumiectus, 2007, 6(3), 61-72, (in Polish). Google Scholar

  • [79]

    Varavipour M., Givehchi S., Mashal M., Heavy metals distributions and uptake in field-grown maize after application of sewage sludge in soil of South Eastern, Iran, Asian J. Chem., 2009, 21(1), 23-30. Google Scholar

  • [80]

    Niu H., Li S., Shen J., Yao M., Characteristics of heavy metal accumulation on fly ash- and sewage sludge-amended calcific soil, Chin. J. Geochem., 2012, 31(2), 181-186. CrossrefGoogle Scholar

  • [81]

    Nafees M., Amin A., Evaluation of heavy metals accumulation in different parts of wheat plant grown on soil amended with sediment collected from Kabul river canal, J. Agric. Res., 2014, 52(3), 383-394. Google Scholar

Footnotes

    About the article

    Received: 2017-09-29

    Accepted: 2017-12-04

    Published Online: 2018-02-13


    Conflict of interest: Authors state no conflict of interest.


    Citation Information: Open Chemistry, Volume 16, Issue 1, Pages 35–49, ISSN (Online) 2391-5420, DOI: https://doi.org/10.1515/chem-2018-0004.

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    © 2018 Magdalena Jastrzębska et al., published by De Gruyter. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License. BY-NC-ND 4.0

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