Introduction
Over the last few years there has been increasing concern about heavy metal(loid) contamination in agricultural soils in China. A national survey conducted from 2005 to 2013 reports that 16% of the soil samples collected from 8 km × 8 km grids across the country exceeded the Chinese environmental quality standards for various contaminants, especially heavy metal(loid)s
[1]. A much more comprehensive survey, focusing on agricultural soils in potentially contaminated areas, has been completed recently, although the results have not yet been published. As previously discussed
[2], the definition of soil contamination is rather subjective because it is difficult to separate natural and anthropogenic sources of contaminants in soils. This is especially true for heavy metal(loid)s as their background levels vary between different soils depending on the parent materials and the pedogenesis processes. In some areas of south-western China, for example, elevated concentrations of cadmium (Cd) in soils are partly attributed to high geogenic background levels of this element
[3]. In general, high iron content in soils is associated with high levels of siderophilic elements such as chromium (Cr), cobalt (Co) and nickel (Ni) from geogenic sources
[4]. Heavy textured soils also tend to contain higher levels of metals such as Cd, Co, copper (Cu), Cr, Ni and zinc (Zn) than light soils, which are not related to anthropogenic contamination
[4]. Considering the difficulties in quantifying geogenic versus anthropogenic sources of heavy metal(loid)s, it is perhaps more pertinent to focus on the assessment and mitigation of the risks of soil contamination and protection of soil against future contamination. Risks of soil contamination with metal(loid)s may arise from transfer of contaminants to the food chain affecting food safety, toxicity to soil microorganisms, fauna and plants causing adverse impacts on the ecological functions of the soil, or transfer of contaminants to surface or groundwaters (Table 1). Transfer of toxic metal(loid)s from soil to the food chain represents one of the most relevant risks of soil contamination which should be assessed and managed carefully to ensure food safety and protect public health.
Cadmium and arsenic are high risk metal(loid)s due to their transfer to the food chain
Not all contaminants are readily transferred from soils to the food chain. There are three barriers in the transfer of toxic elements from soils to the edible parts of food crops, namely, the solubility barrier, the translocation barrier and the phytotoxicity barrier
[5]. Some elements (e.g., Cr(III), mercury (Hg), and plumbum (Pb)) have very low solubility in soil so that they are mostly unavailable for plant uptake. Even when their solubility increases under some specific conditions, plant roots tend to sequester these elements and limit their translocation to the aboveground tissues. Some elements (e.g., Co, Cu, Ni, and Zn) have relatively high solubility in soils and can also be translocated to plant shoots relatively easily. However, excessive accumulation of these elements can cause toxicity to plants and reduce yields (Tab.1), and this also makes them less likely to enter the food chain. Among the heavy metal(loid)s, Cd and arsenic (As) can bypass these three barriers relatively easily and are therefore at high risk of transfer from soil to the food chain
[5,6]. Cd and As are of course also toxic to plants. However, unlike Cu, Ni and Zn, Cd and As can be toxic to animals and humans at levels that do not cause phytotoxicity, due to the effects from chronic exposure. For these reasons, Cd and As are the toxic elements of most concern for soil contamination and food safety. Rice grain from paddy fields contaminated by Hg mining may contain elevated levels of highly toxic methylmercury
[7]. This is because some anaerobic microorganisms in paddy soils can methylate inorganic Hg under anoxic conditions and methylmercury has a greater transferability from soil to rice grain than inorganic Hg
[8] (Table 1).
Rice appears to be particularly problematic with regard to both Cd and As accumulation
[6]. This is because rice has a relatively high uptake of both elements
[9,10] and is also a staple food. A recent total diet study shows that rice contributes 56% of the total dietary intake of Cd for the general population in China, and up to 65% for the population in southern China
[11]. In comparison, wheat and vegetables each contribute 10% to 12% of the total Cd intake for the general population in China. Similarly, rice contributes about 60% of the dietary intake of inorganic As for the Chinese population
[12]. Therefore, reducing Cd and As accumulation in rice is a top priority in the risk management of contaminated soils.
Recent surveys show considerable proportions of rice grain samples collected from some areas in southern China exceeding the maximum permissible limits of Cd and As
[13–19]. In some areas the range and mean values of Cd concentration in rice grain are comparable to those reported for the Itai-Itai disease-affected area in Japan
[19,20]. The maximum permissible limit of Cd in rice grain in China is half of the that recommended by FAO/WHO (0.2 versus 0.4 mg·kg
-1). This strict limit is deemed necessary because of the high consumption rate of rice by the Chinese population
[6]. For example, consumption of 250 g rice per day at a Cd concentration of 0.2 mg·kg
-1 would give rise to a Cd intake of 0.83 µg Cd kg
-1 bodyweight d
-1 (for a person weighing 60 kg), which reaches the tolerable Cd intake limit recommended by FAO/WHO
[6]. In some local populations in southern China, estimated average Cd intakes are well over the tolerable intake limit
[14,19]. Urgent action is needed now to reduce dietary Cd intake in these populations.
Reducing the bioavailability of toxic metal(loid)s in soil
The transferability of toxic elements from soils to the food chain depends on their bioavailability in soils. Bioavailability is influenced by multiple soil and plant factors. One of the key factors affecting Cd bioavailability is soil pH. On average across a range of soils studied, Cd solubility increased 3.5 times when soil pH decreased by one unit
[21]. A paired soil-plant survey shows that the median Cd transfer factor from soil to rice grain (i.e., the ratio of grain to soil Cd concentration) increased 10 times, from 0.08 to 0.85, when soil pH decreased from 7.0 to 5.0
[13]. A survey of Cd concentration in rice grains collected from different provinces in China shows a clear geographical pattern, increasing markedly from the north to the south
[22]. This pattern can be explained by the general trend of increasing soil acidity from the north to the south. Over the last three decades there has been widespread acidification in agricultural soils in many parts of China, caused primarily by the cumulative effects of nitrogen fertilizer applications
[23]. Soil acidification is one of the important reasons why Cd concentrations in rice grains produced in some areas of southern China exceed the maximum permissible limit
[13,14]. Liming with calcium carbonate to increase soil pH above 6.5 has been shown to be highly effective in decreasing grain Cd concentrations, with the effect lasting for at least three years
[19,24]. Liming with calcium carbonate to pH 6.5 had no significant effects on grain yield or As concentrations in the grain
[24]. Liming is the most economical method of reducing Cd transfer in acid soils (Table 1). Other materials may also be used to immobilize Cd and other heavy metals in soils if the cost-benefit analysis is favorable.
Arsenic is a metalloid with a relatively high transferability from paddy soils to rice. This is partly because As is mobilized under anaerobic conditions in submerged paddy soils. The most important factor affecting As bioavailability in paddy soils is the redox status
[25]. Under submerged conditions in paddy soils, reductive dissolution of iron oxyhydroxides releases As sorbed by the minerals and arsenate is also reduced to the more mobile form of arsenite
[26–28]. Growing rice under aerobic conditions can decrease grain As concentrations by more than 10-fold compared to standard flood-irrigated cultivation
[29]. Water saving methods such alternate wetting and drying can be effective at reducing As accumulation in rice
[30–32] (Tab.1). Paddy water management can be an effective method to control As bioavailability, the effect on Cd being opposite to that on As
[32,33]. Draining of paddy water during the grain filling period can lead to greatly increased Cd accumulation in rice grain if the soil is acidic
[34]. Cd is maintained at low solubility under anaerobic conditions due to the precipitation of cadmium sulfide and increased pH
[35]. Once a paddy soil is drained, sulfide is oxidized rapidly and soil pH also decreases, releasing insoluble Cd into the soil solution
[36]. The contrasting biogeochemical behaviors of As and Cd mean that managing the risks of As and Cd in paddy soils simultaneously is a difficult task
[6]. Applications of silicon fertilizers and materials rich in manganese oxides and iron oxides may mitigate both As and Cd
[6] (Tab.1). However, more field studies are needed to assess the efficacy of these materials. Unlike Cd, As availability in paddy soil is not sensitive to pH changes within the acidic to neutral range.
Breeding or engineering crop cultivars with low metal(loid) accumulation
There are large variations within crop germplasm in the ability to accumulate metal(loid)s
[37–39]. Rice cultivars with stably low accumulation of Cd or As have been identified through large scale screening under field conditions
[38]. These cultivars can be used in combination with other agronomic methods such as liming and water management to produce a greater effect on reducing the accumulation of metal(loid)s in the edible parts of crops (Table 1).
Large genetic variations also suggest the possibility of breeding crop cultivars with low accumulation of metal(loid)s in the edible parts. Many quantitative trait loci (QTLs) controlling Cd or As accumulation have been reported
[2,39]. To date, genes underlying several QTLs for Cd accumulation in rice have been cloned
[40–42].
OsHMA3, encoding a tonoplast Cd transporter, is a key gene controlling Cd translocation from roots to shoots and grain in rice; weak alleles of
OsHMA3 are associated with high accumulation of Cd in rice grain
[40,43–45]. Strong alleles of
OsHMA3 can be used to breed low Cd rice cultivars. For example, by introgressing
qCd7 from the
japonica cultivar Nipponbare containing a strong allele of
OsHMA3 to
indica rice hybrids, grain Cd concentration was reduced by about 50%
[46]. QTLs for low Cd and for high selenium (Se) or Zn in grain, beneficial to human nutrition, can be introduced into elite rice cultivars through QTL pyramiding and marker-assisted molecular breeding
[47]. Allelic variation in
BrHMA3 also has an important role in Cd accumulation in the leaves of
Brassica rapa vegetables; strong alleles of
BrHMA3 can be used to breed low Cd
Brassica vegetables
[48]. Breeding low As rice cultivars is more challenging because contributions of various As QTLs are small and none of them have been cloned yet. Studies using reverse genetics have shown a number of key genes controlling As uptake and translocation in rice, such as silicon transporters for arsenite uptake
[49] and tonoplast transporters for vacuolar sequestration of arsenite-phytochelatin complexes
[50]. However, it is not yet known if allelic variations in these genes within rice germplasm can cause variations in As accumulation in rice grain.
Genetic engineering techniques can also be used to reduce Cd and As accumulation in rice grain
[6]. Knockout of
OsNRAMP5, encoding a major influx transporter for both Mn and Cd
[51], using CRISPR/Cas9 gene editing technology can decrease Cd accumulation in rice grain by more than 90%
[52]. Overexpression of functional
OsHMA3 is also highly effective at reducing Cd accumulation in rice grain by more than 90%
[40,53]. Overexpression of a rice aquaporin gene
OsNIP1;1 or of
OsABCC1 together with a bacterial
g-glutamylcysteine synthetase gene has also been shown to reduce As accumulation in rice grain significantly
[54,55]. Although technologically feasible and highly effective, genetically engineered crops are not yet allowed in many countries.
Need for long-term monitoring and model predictions
While the risks of soil contamination can be managed to a certain extent, it is important to protect agricultural soils from contamination in the future. Anthropogenic additions of heavy metal(loid)s may lead to slow accumulation of these elements in soils. Gradual increases in the concentrations of metal(loid)s in soils are often difficult to detect over a relatively short period of time. Long-term monitoring of both anthropogenic additions and accumulation in soils is necessary. Long-term experiments at Rothamsted, UK, have shown that long-term applications of phosphate fertilizers resulted in significant increases in the concentrations of Cd and As in the soil
[56–58]. It is well known that phosphate fertilizers may contain considerable amounts of Cd, although fortunately, rock phosphates in south-west China generally contain very low levels of Cd
[2,59]. Imported phosphate fertilizers may have higher levels of Cd, which need to be monitored and regulated. It is a surprise that applications of phosphate fertilizers nearly doubled soil As concentration at the Rothamsted long-term experiment because phosphate fertilizers were not known to contain high levels of As
[57]. However, analysis of archived samples shows very high concentrations of As in the phosphate fertilizers used in the experiment during the period from 1925 to 1947, suggesting historical As contamination
[57]. In another example of long-term experiments in China, applications of pig manure for 16–17 years increased Cd concentrations in the soils more than 10-fold, most likely due to Cd contamination in the Zn minerals added to animal feeds
[60]. In addition to fertilizers and manures, atmospheric deposition and irrigation water may also contribute considerably to the addition of metal(loid)s to soils and should be monitored
[2,61]. Changes in the concentrations of metal(loid)s in soils also depends on the losses, such as plant uptake and removal, leaching and runoff. While plant uptake and removal are easily quantifiable, data on leaching and runoff of metal(loid)s and their relationships with soil properties and climatic variables are scarce. More studies are needed to establish and verify predictive models of leaching and runoff of metal(loid)s. Mass balance models can then be constructed to predict future trends of metal(loid)s in soils at a regional scale and under different scenarios
[62,63]. A scenario that may lead to a gradual decrease in Cd concentrations in paddy soils is the removal of rice straw
[62,63], although this practice would reduce the inputs of organic matter to the soil. In Europe, modeling of the future long-term changes in soil Cd concentrations in agricultural topsoils predicts either increases, decreases or little changes in soil Cd concentration over the next 100 years depending on the region and scenario
[64,65]. The modeling outcomes have been used to guide European Union legislation on Cd limits in phosphate fertilizers. Compared with Europe, measurements in China have shown considerably larger additions of Cd and other metal(loid)s from atmospheric deposition and manure applications, but smaller additions from phosphate fertilizers
[61,64–66]. Reducing the addition of Cd and other contaminants into agricultural soils is a top priority.
The Author(s) 2020. Published by Higher Education Press. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0)