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Environmental Pollution 267 (2020) 115653

Contents lists available at ScienceDirect

Environmental Pollution
journal homepage: www.elsevier.com/locate/envpol

Review

Microplastics could be a threat to plants in terrestrial systems directly


or indirectly*
Noreen Khalid a, *, Muhammad Aqeel b, Ali Noman c
a
Department of Botany, Government College Women University, Sialkot, Pakistan
b
State Key Laboratory of Grassland and Agro-ecosystems, School of Life Science, Lanzhou University, Lanzhou, Gansu, PR China
c
Department of Botany, Government College University, Faisalabad, Pakistan

a r t i c l e i n f o a b s t r a c t

Article history: Microplastics (MPs) are an emerging threat to ecosystem functioning and biota. The major sources of
Received 27 May 2020 MPs are terrestrial and agricultural lands. But their fate, concentration in the terrestrial environment, and
Received in revised form effects on soil and biota are poorly understood. There is a growing body of concern about the adverse
15 August 2020
effects of MPs on soil-dwelling organisms such as microbes in mycorrhizae and earthworms that mediate
Accepted 12 September 2020
Available online 16 September 2020
essential ecosystem services. Environmental concentrations and effects of MPs are considered to increase
with increasing trend of its global production. MPs in the soil could directly impact plants through
blocking the seed pore, limiting the uptake of water and nutrient through roots, aggregation, and
Keywords:
Sorbed chemicals
accumulation in the root, shoot, and leaves. However, MPs can also indirectly impact plants by affecting
Microplastic uptake soil physicochemical characteristics, soil-dwelling microbes, and fauna. An affected soil could impact
Phytotoxicity plant community structure and perhaps primary production. In this article, we have assessed the po-
Emerging pollutant tential direct and indirect impacts of MPs on plants. We have discussed both the positive and negative
impacts of MPs on plants in terrestrial systems based on currently available limited literature on this
topic and our hypothetical understandings. We have summarized the most current progress in this re-
gard highlighting the future directions on microplastic research in terrestrial systems.
© 2020 Elsevier Ltd. All rights reserved.

1. Introduction They are divided into two main types based on their origin, for
example, MPs produced through grinding are known as primary
In landfills, plastic items can take up to 1000 years to decom- MPs. Abrasives in consumer products such as creams, showering
pose. Isn’t it scary? Among all the anthropogenic changes to the gels, shampoos, cleansers, and tooth pastes all have adequate
surface of our earth, microplastic pollution is perhaps the most quantities of primary microplastics (Browne, 2015). On the other
long-lasting. Oceans have been discovered to be the sinks of hand, secondary microplastics are produced through physical,
microplastic particles after about a decade of research. MPs are now biological or chemical degradation of larger plastic items (Cooper
ubiquitous in the oceans and cause potential adverse effects on and Corcoran, 2010). Secondary MPs can be formed with the help
marine organisms (Galloway et al., 2017). But where these plastic of microbial, UV, or mechanical degradation in the soil. MPs can
pollutants are coming from? It is estimated that in oceans, 80% of also have varying shapes such as beads, films, granules, and fibers
microplastic pollution is coming from land (Li et al., 2016). Re- based on their sources.
searchers have now recently extended their research on MPs to Soils have been a long term and probably major sinks of MPs in
terrestrial environments. But until now only a handful of studies terrestrial ecosystems (David et al., 2018; Hodson et al., 2017;
have been reported on MPs in terrestrial habitats. Horton and Dixon, 2018). Only arable soils may have more MPs than
MPs particles are smaller than 5 mm in size (Alimi et al., 2018). the world’s oceans (de Souza Machado et al., 2018). Sewage sludge
has been found to contain large quantities of fragments and mi-
crofibrils of MPs (De Falco et al., 2018; Li et al., 2018; Sun et al.,
2019). The application of sewage sludge in agricultural fields is
*
This paper has been recommended for acceptance by Baoshan Xing.
considered as a cheap fertilizer and is a common practice on large
* Corresponding author. scales in developing countries (Corradini et al., 2019; Mai et al.,
E-mail addresses: noreenbasra@gmail.com, noreen.khalid@gcwus.edu.pk (N. Khalid). 2018). Primary MPs are produced intentionally in various

https://doi.org/10.1016/j.envpol.2020.115653
0269-7491/© 2020 Elsevier Ltd. All rights reserved.
N. Khalid, M. Aqeel and A. Noman Environmental Pollution 267 (2020) 115653

industrial and cosmetics products (Napper et al., 2015). However, differently in the soil. Generally MPs have lower densities than the
the large scale sources of MPs are secondary MPs that are produced soil particles of their size. Therefore, they tend to lower soil bulk
by the weathering and degradation/disintegration of larger plastic density. De Souza Machado and co (de Souza Machado et al., 2018)
products such as plastic bags, sheets, and bottles (Rillig, 2012). Road reported a reduction in soil bulk density with contamination with
traffic dust, littering, diffused atmospheric deposition, industrial microplastic microfibers. This can substantially increase the soil
products, laundry effluents, and sedimentation from irrigation aeration which may help in root penetration into the soil. On the
waters are some of the important sources of MPs in the environ- other hand, microfibers can also entangle the juvenile roots and
ment (Duis and Coors, 2016). The average microplastic particles could be a hindrance to the growth of seedlings. Increased soil
concentration in an established riparian forest is 18,760 particles aeration may also enhance aridity at the soil surface which can also
kg1 in southwestern China (Zhang and Liu, 2018), 78 particles kg1 adversely affect growth and development of seedlings (Wan et al.,
in farmland soils in suburbs of Shanghai (Liu et al., 2018), 2019). Microplastic thin films can create water channels making
420e1290 MP items/kg soil in agriculture surface soils (Li et al., rapid percolation of water to deeper soil layers. Besides, these films
2019), 320 to 12,560 items/kg DW in vegetable farmlands in also induce the formation of desiccation cracks in the surface soil
Wuhan (Chen et al., 2020a), 20.6 to 529.3 items/kg in rural and (Wan et al., 2019) (Fig. 1).
urban roadside dust in Victoria, Australia (Su et al., 2020), 88 to MPs might alter the physical properties of the soil, for instance,
605 MPs per 30 g dry dust in street dust in Tehran, Iran (Dehghani by reducing or boosting up the cohesion between aggregate
et al., 2017), and 90% of Swiss floodplain soils are found to be -forming soil particles. The contribution of microfibers in the pro-
contaminated with MPs (Scheurer and Bigalke, 2018). The current cess of aggregates formation is the most important in this regard.
estimation is that MPs are present everywhere in terrestrial eco- According to Zhang and Liu (2018), 72% of MPs in soil take part in
systems but data on microplastic studies in soils is limited. Field aggregates formation. In a recent investigation, Lozano and Rillig
studies are suggested to better understand the effects, sources, and (2020) revealed a change in plant community structure in micro-
fate of MPs in the terrestrial environments. fiber contaminated soil. They revealed that MPs could affect plant
The persistence, ubiquity, variety, and abundance of MPs are a species dominance as Calamagrostis (European invasive species),
serious environmental risk to the soil. In the oceans  where fate, and Hieracium (allelopathic species) became dominant in microfi-
chemistry, and toxicity of MPs is well documented  MPs affect ber rich soil. However, plant species such as Holcus can facilitate a
physicochemical processes of the surrounding environment with healthy plant community structure decreased in biomass. These
adverse effects on marine biota. MPs come in different sizes, effects in the plant community level could be due to secondary
shapes, structures, additives, and surface topographies such as effects caused by microfibers such as drought.
microfibrils, beads, pellets, granules, films, foams, and fragments Polyester fibers (PFs) also induce aggregation of soil particles by
(Fig. 2a). These different types of MPs may influence soil physical holding them through heaping (de Souza Machado et al., 2018;
structures, for example, soil bulk density, aeration, and water Zhang et al., 2019). However PFs do not take part in aggregate
holding capacity, etc. Besides affecting the physical structure of the formation in sandy soils (Lehmann et al., 2019). PFs also increase
soil, MPs may potentially impact soil biogeochemistry in various the water holding capacity of the soil because of aggregates for-
ways. Chemical additives used in the manufacturing of MPs could mation. However, the other microplastic particles such as beads,
be toxic to soil-dwelling microflora and fauna (Rillig and fragments, or polyacrylic fibers do not influence the soil aggrega-
Bonkowski, 2018). Additionally, MPs can sorb toxic organic and tion nor water holding capacity. The addition of PLA and HDPE
inorganic compounds from the surrounding environment making directly affects the binding mechanism of soil particles by forming
them contaminated surfaces in the soil (Hüffer et al., 2019; Zhou stable soil aggregates (Boots et al., 2019). The formation of soil
et al., 2019). Any change in physicochemical characteristics of soil aggregates substantially increases soil aeration and porosity. We
could be translated to linked biota. Initially, some studies have hypothesize that this kind of soil physical structure would be an
demonstrated the toxic effects of MPs on earthworms, microbes, ideal environment for the growth and development of plant roots
and plants (Qi et al., 2018; Rodríguez-Seijo et al., 2018; Wang et al., since it also holds moisture efficiently. But Boots et al. (2019), found
2019a, 2020; Yi et al., 2020). The tiny microplastic particles in the a reduction in root growth of Lolium perenne on exposure to LDPE
soil have the potential to impact plant community structure and MPs. However, this remains unclear whether this alteration in root
ecosystem functioning (Lozano and Rillig, 2020). But the potential growth is due to change in soil physical structure or due to some
impacts of MPs on plants remain largely unexplored and there is other toxic chemical properties of MPs? Further research is needed
not much information on this perspective. We assume that there to understand the effects of MPs on soil-plant systems.
are several possible ways by which MPs can directly and indirectly
impact plants, and crops. Because MPs are persistent and they will 1.2. Microplastic uptake: direct toxicity to plants
remain in the environment for a long period, so there is an urgent
need to uncover their potential impacts on plants. The aim of Plants grown in agricultural soils are directly exposed to MPs
writing this article is to identify the areas, opinions, and facts in the when plastic mulching, sewage sludge as fertilizer, and organic
research gap where MPs research on plants can be pushed forward. manures are applied (Watteau et al., 2018). Recently, a few studies
have reported the direct impacts of MPs on plants that have been
1.1. Alteration in soil structure: impacts on root growth summarized in Table 1. Root growth and seed germination are
important factors while evaluating the direct effect of MPs on
MPs can be transported inside the soil (Rillig et al., 2017). The plants. Microplastic particles of bigger size (100 nm-5mm) can be
texture of the soil and size of the MPs govern the mobility of MPs in indirectly harmful to plants through modifying and/or disrupting
the soil (O’Connor et al., 2019). The transport of MPs mainly occurs the soil structure. But it can also affect directly through clogging the
through bioturbation, preferential flow, cracks in soils, and because seed pores (Bosker et al., 2019). It can slow down or completely
of various agricultural practices like plowing, ditching, tilling, etc inhibit the uptake of water by adhering to the surface of seed pores.
(Lwanga et al., 2017; O’Connor et al., 2019; Rillig, 2018; Rillig et al., Bosker et al. (2019) reported a 78% reduction in seed germination
2017; Zhu et al., 2018c). However, this transport will probably not process after 8 h of exposure to three different sized plastic parti-
be significant in fine-grained homogeneous clayey soils. Since MPs cles (50, 500, and 4800 nm) at a concentration of 103e107 particles
are of different types having specific densities, they behave ml1. This reduction in the rate of germination was due to the
2
N. Khalid, M. Aqeel and A. Noman Environmental Pollution 267 (2020) 115653

Fig. 1. MPs effects on physicochemical characteristics of the soil that affect growth of plants.

physical blockage of the seed pores by MPs. This was demonstrated both of these locations, microbeads adhered to each other making
with the use of fluorescent dyes and confocal microscopy. They also chains and bunch like structures. However in the leaf, they found to
saw accumulations of MPs on root hairs later. be uniformly dispersed. In all of the above studies, broad bean,
MPs after degradation convert into even smaller sized plastics wheat, and lettuce plants were exposed to MPs microbeads in
known as nanoplastics. Could these smaller nanoplastics be aqueous solutions i.e. either in the form of hydroponics (lettuce,
absorbed by the plants with water from the soil? This was not wheat) or aqueous solution was applied with soaked cotton/filter
known until recently a few studies have demonstrated the uptake papers (broad beans). None of these studies grew the plants in true
of MPs by terrestrial plants. Accumulation of MPs (100 nm) in roots soil conditions. If these crop plants showed the uptake of MPs
of broad bean (Vicia faba) was seen with laser confocal scanning through aqueous solutions, what would be the results if they were
microscopy (Jiang et al., 2019). In this experiment, MPs might have grown in soil contaminated with MPs? Chae and An (2020) directly
blocked cell wall pores or cell connections for the transport of water exposed the mung bean (Vigna radiata) to nano plastic contami-
and nutrients. Because the plant significantly showed increased nated soil and observed an 83.3% reduction in the root growth at a
antioxidant enzyme activities and decreased growth as a result of concentration of 100 mg kg1 nano plastics in the soil. They also
microplastic accumulation. Li et al. (2020) demonstrated the reported the accumulation of nano plastic particles in the leaves of
localization of fluorescently labelled MPs within the whole plant mung bean. The contaminated mung bean plant then badly
tissues in wheat (Triticum aestivum). The PS microplastic microbe- impacted the growth rate of the African giant snail (Achatina fulica)
ads were seen in the root, shoot, and leaves by using a confocal laser which was fed on it. Hence, MPs are likely to be ingested by the
scanning microscope in this study. In another study, uptake, dis- herbivores with their plant food, whether absorbed in the plant or
tribution, and migration of fluorescent polystyrene microbeads adsorbed on the surface. There is a dire need to understand the
(0.2 mm) in lettuce were investigated (Li et al., 2019). It was reported in vivo effects of microplastics for a wide range of food crop plants
that microbeads were trapped in the root cap extracellularly, visible especially the root edible crops.
as a dark green tip to the naked eye. Confocal microscopy revealed
the localization of microbeads in cell wall tissue of the root and
vascular system indicating the intercellular space passage of 1.3. Effect on soil microbial activity: potential reduced fertility
microbeads through apoplastic transport. Microbeads also moved
through the vascular system following the transpiration stream. In Microplastic contamination of soils could affect properties of
soil (as described previously), change biophysical and geochemical
3
N. Khalid, M. Aqeel and A. Noman Environmental Pollution 267 (2020) 115653

Fig. 2. a. Different types of MPs; b. interaction of inorganic and organic pollutants with MPs impact plants and soil-dwelling organisms. HMs (heavy metals), POPs (persistent
organic pollutants), As (arsenic), Cd (cadmium), Zn (zinc), DDT (dichlorodiphenyltrichloroethane), CPF (chlorpyrifos), PCB (polychlorinated biphenyl), U-for (urea-formaldehyde).

environments. This can substantially influence the functional and recommended.


structural diversity of soil microbial communities causing serious Studies have revealed the adverse effects of PFs (0.05e0.4%),
potential soil environmental problems (Rillig and Bonkowski, 2018; polyacrylic (0.05e0.4%), and PS (polystyrene) (1 mg kg1) micro-
Rillig et al., 2019). This includes the functional diversity of soil en- plastic particles on microbial communities in the soil (Awet et al.,
zymes and microbiota (Awet et al., 2018). This change in soil 2018; de Souza Machado et al., 2018). However, PP (poly-
structure and composition may also affect the fertility of the soil by propylene) (7% and 28%) found to be positively impacting bacterial
reducing the growth of microbial communities in the rhizosphere growth in the soil (Liu et al., 2017). Changes in microbial activity in
(Qi et al., 2020). The rhizosphere is an important interface where these studies have been proposed to be because of modified soil
plants interact with beneficial and harmful microbial communities structure. However, the data on MPs and microbial communities in
in the soil. The interaction of soil microorganisms with MPs in the the soil is extremely limited. Further investigations are strongly
rhizosphere largely remains unexplored. Different sized MPs affect recommended to understand the effects and linkage of MPs with
interactions between plants and microbial communities differently microbial communities in the soil.
though. This behaviour occurs due to variations in surface to vol- Microbial communities in the soil such as arbuscular mycor-
ume ratios of microplastic particles (Brodhagen et al., 2017). rhizal fungi, and nitrogen-fixing bacteria have a direct impact on
However, there is only a little information available on general plant growth. Reduced microbial activity by MPs could directly
microbial activity in soil influenced by MPs. impact plant and crop growth (Powell and Rillig, 2018). MPs affect
MPs affect the microbial communities in their vicinity in the soil. the relative abundance and community structure of arbuscular
Like aquatic environments, MPs generally have been found to mycorrhizal fungi in the soil (Wang et al., 2020). Interactions be-
decrease microbial activity in the soil (Rillig, 2018; Yang et al., tween constituent microbial species in the soil also found to be
2018). HDPE (high-density polyethylene) contamination of soil impacted by PLA MPs (Chen et al., 2020a). This could affect mi-
decreases soil pH which could impact microbial growth (Bandow crobial assisted mineral absorption and nitrogen fixation rates.
et al., 2017; Boots et al., 2019). However, other recent studies Additionally, MPs adversely affect soil enzymes such as urease,
have reported an increase in soil pH and reduction in soil EC in, PE glucosidase, and phosphatase (Yang et al., 2018). Fei et al. (2020), on
(polyethylene), PLA (polylactic acid), and LDPE (low-density poly- the other hand, found a positive impact of PE (polyethylene) and
ethylene) contaminated soils (Qi et al., 2020; Wang et al., 2020). PVC (polyvinyl chloride) MPs on acid phosphatase and urease ac-
Changes in soil pH are highly likely to cause alterations in microbial tivities in the soil.
communities of the rhizosphere and those present in the bulk soil, MPs have a great ability to host unique bacterial species than the
by interfering with the composition and diversity of soil microor- surrounding soil particles. Bacterial communities dwelling on MPs
ganisms (Rousk et al., 2009). But the mechanism by which MPs are structurally different from surrounding MPs, plant litter, and
change the pH of the soil is unknown. Further study to understand soil particles. Surfaces of microplastic particles like flakes and pits
this change in pH under the influence of MPs is highly suggest as active hydrolysis sites where various microbes colonize.

4
N. Khalid, M. Aqeel and A. Noman Environmental Pollution 267 (2020) 115653

Table 1
Studies on impacts of MPs on terrestrial plants.

Plant species Plastic type Concentration Exposure Effects Reference

Perennial ryegrass (Lolium perenne) Biodegradable PLA (density of 0.1% w/w and 30 days Reduction in shoot height and biomass, fewer Boots et al.
1.2e1.3 g cm3), virgin HDPE 0.001% w/w seeds germinated (2019)
(density of 0.95 g cm3)
microplastic clothing fibers
Garden cress (Lepidium sativum) 4800 nm MP 103 to 107 particles 8 and Accumulated on the root hairs, Bosker
mL1 24 h germination rate was significantly reduced, et al.
physical blockage of the pores in the seed (2019)
capsule
Oat (Avena sativa), radish (Raphanus sativus) PEIs including PEtOx as an N- 100, 250, 500, 750, 6 Nitrogen released from the tested PEIs and LPEI Rychter
acyl-substituted PEI, LPEI and and 1000 mg kg1 of months but no harmful effect, harmful to plants only at et al.
BPEI soil dry weight high concentrations (2019)
Broad bean (Vicia faba) PS (5 mm, 100 nm) 10, 50 and 48 h Genotoxic and oxidative damage, decreased Jiang et al.
100 mgL1 biomass and catalase (CAT) enzymes activity, (2019)
increased activities of superoxide dismutase
(SOD) and peroxidase (POD) enzymes, blocked
cell connections or cell wall pores for transport
of nutrients in roots
Mung bean (Phaseolus radiates), lettuce Macro EPS 60 EPS particles for 28 days Low levels of interaction with the crop- Kim et al.
(Lactuca sativa), and rice (Oryza sativa) 8.3 ± 0.5 mm þ adsorbed Cd each treatment, dependent water absorption rate, did not (2019)
5.313 ± 0.445 Cd induce adverse effects on the crop
mgL1 in DW
Wheat (Triticum aestivum) LDPE and starch-based 1% (w/w) 2 and 4 Vegetative and reproductive growth affected Qi et al.
biodegradable plastic months (2018)
Grasses (Festuca brevipila, Calamagrostis PFs, length 1.28 ± 0.03 mm and 12 g of microfibers 2 Species dominance seen, Calamagrostis and Lozano
epigejos, and Holcus lanatus) and herbs diameter ~30 mm into 3 kg of soil months Hieracium became dominant, while, Holcus and Rillig
(Achillea millefolium, Plantago lanceolata, decreased in biomass (2020)
Hieracium pilosella, and Potentilla argentea)
Maize (Zea mays L.) PE, PLA 0.1%, 1% and 10% (w/ 1 month PLA decreased maize biomass and chlorophyll Wang
w) content in leaves, PE and PLA caused increase in et al.
pH and DTPA-extractable Cd concentrations in (2020)
soil, altered AMF community structure and
diversity, PLA caused stronger phytotoxicity
Garden cress (Lepidium sativum) PP, PE, PVC 0.02% (w/w) 21 days Occurrence of oxidative burst, PVC proved the Pignattelli
most toxic et al.
(2020)
Lettuce (Lactuca sativa L., Rosa) PS microbeads (0.2 and 1.0 mm) 50 mg L1 14 days Adherence, uptake, accumulation, and Li et al.
translocation of MPs in the vascular tissue (2019)
Onion (Allium fistulosum) PA beads 15e20 mm, PFs PFs 0.2% of soil fresh ~2 Significant changes in plant biomass, root traits, de Souza
5000 mm long and 8 mm weight. All the other months tissue elemental composition, soil microbial Machado
diameter, PEHD and PP virgin MPs at 2.0% of soil activity et al.
pellets 2e3 mm spheres fresh weight (2018)

PEIs (polyethylenimines), PEtOx (poly 2-ethyl-2-oxazoline), LPEI (linear polyethylenimine) and BPEI (branched polyethylenimine), EPS (expanded polystyrene), LDPE (low-
density polyethylene), PE (polyethylene) and PLA (polylactic acid), AMF (Arbuscular mycorrhizal fungi), PP (polypropylene), PE (polyethylene), PVC (polyvinylchloride), PA
(polyamide), PEHD (polyethylene high density), PP (polypropylene), PS (polystyrene).

Thus MPs provide distinct ecological niches for soil bacteria (Chai decade.
et al., 2020). Zhang et al. (2019) investigated the bacterial com- To modify the properties of plastics such as color, ultraviolet
munity composition on MPs in farmland soils and found Chloroflexi, resistance, flame retardancy, and flexibility, various organic and
Acidobacteria, Bacteroidetes, and Gemmatimonadetes bacteria inorganic additives are added to the plastic during its
actively colonizing microplastic particles. According to Zhang et al. manufacturing (Cole et al., 2011; Kwon et al., 2017). These additives
(2019), these bacteria are known as “KeyStone Species” among may include flame retardant polybrominated diphenyl ether
bacterial communities and MPs serve as “special microbial accu- polymers, acid scavengers, lubricants, light and heat stabilizers,
mulators”. Similarly, Huang et al. (2019) also revealed that MPs pigments, slip compounds, antistatic agents, antioxidants, and
provide unique habitats for special microbial communities such as plasticizers (Hahladakis et al., 2018). It means plastics already
pathogens and plastic-degrading bacteria which can alter the contain a variety of chemical contaminants before they enter into
ecological functioning of the soil ecosystem and play role in MPs the natural environment. Additionally, MPs are considered as car-
degradation. Arthrobacter, Streptomyces, Nocardia, Aeromicrobium, riers or vectors of many organic and inorganic chemical contami-
Janibacter, and Mycobacterium were also found to be more prone to nants in the environment (Bakir et al., 2016; Browne et al., 2007;
inhabit surfaces of MPs in soil (Yi et al., 2020). Wang et al., 2019c). Few studies have determined the presence of
toxic heavy metals on MPs in the aquatic environments (Brennecke
1.4. Chemically rich particles: is that a risk? et al., 2016; Hodson et al., 2017), where they have proved to pose a
threat to aquatic biota (Table 3). Various heavy metals such as Pb,
Ecotoxicological concerns about MPs have been raised because Cd, Cu, Cr, Hg, Ag, Fe, Sb, and Mn have also been found on MPs in
they act as both sources and sinks of toxic chemicals in the envi- highly significant concentrations in a variety of habitats (Zhou et al.,
ronment. This includes the potential toxicity caused by plastic ad- 2019). Kim et al. (2019) performed a pot experiment to study the
ditives and various organic and inorganic chemicals they sorb from impact of Cd adsorbed on expanded PS MPs on mung bean, lettuce,
their surroundings (Xu et al., 2019). These potential risks of MPs and rice crops. They didn’t find any significant adverse effects on
toxicity have been a discussion of scientific debate for about a these crops but the effect on water absorption by roots was mainly

5
N. Khalid, M. Aqeel and A. Noman
Table 2
Studies on impacts of MPs on soil biota.

Organism Plastic type Concentration Exposure Effects References

Redworm (Eisenia andrei) PE 62.5, 125, 250, 500 and 1000 mg kg1 soil DW 28 days Damages gut and immune system Rodriguez-Seijo
et al. (2017)
Collembolan species (Folsomia PET fibers and urea-formaldehyde particles 5 mg of the 100e200 mm fraction and 2.5 mg 7 days Cause bioturbation in soil, could bioaccumulate these Maaß et al.
candida and Proisotoma minuta) of the <100 mm fraction microplastics pollutants in food web (2017)
Earthworm (Eisenia fetida) PE, 300 mm, and PS  250 mm 1, 5, 10, and 20% DW 14 days Increased activity of peroxidase, catalase, and the level of Wang et al.
lipid peroxidation (2019b)
Earthworm (Eisenia fetida) LDPE 62, 125, 250, 500 and 1000 mg MP kg1 soil 28 days Oxidative stress Rodríguez-Seijo
DW et al. (2018)
Earthworms (Eisenia fetida) LDPE (5 mm and 0.25 mme1 mm) and CPF 180e200 MPs particles of 5 mm and CPF 9.9 14 days no evidence of MPs or CPF uptake, Rodríguez-Seijo
e50 mg kg1 soil DW but inhibition of TBARs and AChE et al. (2019)
Earthworm (Lumbricus terrestris) PE < 150 mm 7, 28, 45, and 60% soil DW 60 days Growth rate was significantly reduced, mortality increased Lwanga et al.
(2017)
Earthworm (Lumbricus terrestris) Microfibres 1.0% w/w 35 days Burrowing and feeding behaviour modulated Prendergast-
Miller et al.
(2019)
Common PVC particles 80 and 250 mm in diameter 1 g microplastics kg1 soil 56 days Collembolan growth and reproduction were significantly Zhu et al.
soil collembolan (Folsomia inhibited (2018b)
candida)
Earthworms (Eisenia fetida) PS 100 nm and 1300 nm fluorescent particles 100 and 1000 mg of microplastics per kg of 14 days Induced DNA damage in earthworms Jiang et al. (2020)
artificial soil
6

Earthworms (Lumbricus terrestris) LDPE 7% by weight Mobilised microplastic transport from the surface into the Yu et al. (2019)
soil
1
Earthworms (Eisenia fetida) LDPE < 400 nm 0.1, 0.25, 0.5, 1.0, 1.5 g kg soil DW 28 days Catalase activity and malondialdehyde content increased, Chen et al.
acetylcholine esterase was significantly stimulated (2020b)
Terrestrial snails (Achatina fulica) PET microplastic fibers 0.01e0.71 g kg1 soil DW 28 days Reduced glutathione peroxidase and total antioxidant Song et al. (2019)
capacity, but elevated malondialdehyde
Soil oligochaete (Enchytraeus PS (0.05e0.1 mm particle size) 10% 7 days Significant reduction in relative abundance of Rhizobiaceae, Zhu et al. (2018a)
crypticus) Isosphaeraceae and Xanthobacteraceae families
1 € pfer et al.
Bacterivorous LDPE (diameter ± standard deviation: 1, 10, and 100 mg MP L ~6 days Reproduction affected Scho
nematode (Caenorhabditis 57 ± 40 mm), PLA and PBAT (40 ± 31 mm) (2020)
elegans)
Soil enzymes (Urease, catalase, and LDPE 2000 fragments kg1 soil 15 days Urease and catalase activities significantly increased, no Huang et al.
invertase) alteration of invertase activities (2019)
Soil enzymes (urease, membranous PE, fibrous PP and microsphere Microsphere PP were 2 mg g1, other 2 were e Significantly altered microbial community structure Yi et al. (2020)
dehydrogenase, and alkaline PP 20 mg g1
phosphatase)
Springtails (Lobella sokamensis) PS microbeads of three different sizes (0.47 8 mgkg1 2 weeks Disrupts the movement and behaviour of springtails Kim and An

Environmental Pollution 267 (2020) 115653


e0.53 mm, 27e32 mm, and 250e300 mm) (2019)
Springtail (Folsomia candida) PE < 500 mm 0.5% and 1% microplastics (w/w in dry soil) 28 days Change in gut microbial community, inhibited the Ju et al. (2019)
reproduction
Terrestrial worm (Enchytraeus PA (13e18 and 90e150 mm), PVC particles PA 20, 50, 90 and 120 g kg1, PVC 90 g kg1 21 days Reproduction was reduced by PA Lahive et al.
crypticus) (106e150 mm) (2019)

PE (Polyethylene), PET (polyethylene terephthalate), LDPE (low-density polyethylene), CPF (chlorpyrifos), AChE (Acetylcholinesterase), TBARS (thiobarbituric acid reactive substances), PLA (polylactide), PBAT (poly butylene
adipate-co-terephthalate), PP (polypropylene), PA (polyamide).
N. Khalid, M. Aqeel and A. Noman
Table 3
Impact of MPs and sorbed organic and inorganic chemicals on terrestrial organisms and plants.

Chemical Plastic type Organism Concentration Exposure Effects References


1
As(V) PVC Earthworm (Metaphire As 40 mg kg dry soil, MPs 28 days Microplastics alleviated the effect of arsenic on the gut microbiota possibly through Wang et al.
As(III) californica) 2000 mg MP kg1 dry soil binding As(V) and lowering bioavailability of arsenic (2019a)
As (III) PS, PTFE Rice (Oryza sativa) 1.6, 3.2, or 4.0 mg L1) of As(III), PS 17 days Inhibited growth of rice seedlings, inhibited biomass accumulation by inhibiting root Dong et al.
and PTFE sizeof 10 micro m at 0.04, activity and RuBisCO activity, inhibited photosynthesis (2020)
0.1, or 0.2 g L1
Cd PP Earthworm (Eisenia foetida) MP 300, 3000, 6000, and 14, 28, Combined exposure to MPs and Cd posed higher negative effect Zhou et al.
9000 mg kg1 dry soil, 8 mg kg1 Cd and 42 (2020)
days
Cd Macro EPS Mung bean (Phaseolus radiates), 60 EPS particles for each treatment, 28 days Low levels of interaction with the crop-dependent water absorption rate, did not induce Kim et al.
1
8.3 ± 0.5 mm lettuce (Lactuca sativa), and rice 5.313 ± 0.445 Cd mgL in DW adverse effects on the crop (2019)
(Oryza sativa)
7

Cd PE and PLA Maize (Zea mays L.) 0.1%, 1% and 10% (w/w) MP, 5 mg Cd/ 1 month PLA decreased maize biomass and chlorophyll content in leaves, PE and PLA caused Wang et al.
kg soil increase in soil pH and DTPA-extractable Cd concentrations, altered AMF community (2020)
structure and diversity, PLA produced stronger phytotoxicity
Zn HDPE Earth worm (Lumbricus 0.35% of Zn-bearing microplastic 28 days Increased metal exposure in earthworms, non-significant risk Hodson
terrestris) (236e4505 mg kg1) et al.
(2017)
CPF LDPE (5 mm Earthworms (Eisenia fetida) 180e200 MPs particles of 5 mm and 14 days No evidence of MPs or CPF uptake, Rodríguez-
and 0.25 mm CPF 9.9e50 mg kg1 soil DW but inhibition of TBARs and AChE Seijo et al.
e1 mm) (2019)
Sewage sludge HDPE, PET, Earthworm (Eisenia fetida) 10% w/w of plastic, 1% w/w organic 3 or 9 No significant effect on earthworm growth, mortality Judy et al.
organic PVC sludge months (2019)
contaminants

Zn (Zinc), As (Arsenic), Cd (Cadmium), CPF (Chlorpyrifos), PE (Polyethylene), EPS (Expanded Polyethylene), PS (Polystyrene), PP (Polypropylene, HDPE (High Density Polyethylene), PVC (Polyvinyl Chloride), PET (Polyethylene
Tetra Phthalate), PTFE (Polytetrafluoroethylene), PE (Polyethylene), PLA (Polylactic Acid), AMF (Arbuscular Mycorrhizal Fungi).

Environmental Pollution 267 (2020) 115653


N. Khalid, M. Aqeel and A. Noman Environmental Pollution 267 (2020) 115653

Fig. 3. MPs in the soil affect plant growth directly or indirectly by impacting the growth of soil-dwelling organisms.

crop dependent. Wang et al. (2020), on the other hand, found se- activities also increase soil porosity thus plant roots are facilitated
vere phytotoxicity in maize caused by Cd spiked PE and PLA MPs in with better gas exchange. Hence, the growth of plants may be
the soil. However, further research is required to understand the decreased by the reduction in the number and activity of these soil
desorption rate of other heavy metals on a wide range of terrestrial organisms (Lwanga et al., 2017). However, Rodríguez-Seijo et al.
plants. (2019) reported no evidence of microplastic uptake or accumula-
Organic chemicals in the soil have a special affinity for MPs tion of pesticide in earthworm (Eisenia fetida) in a controlled
because both of these compounds are hydrophobic. Organic com- experiment. Similarly, it is also possible that MPs could keep all the
pounds such as antibiotics, DDTs (dichlorodiphenyltrichloro- toxic contaminants from the plant roots by sorbing them. This can
ethane), PCBs (polychlorinated biphenyls), PAHs (polycyclic exert a positive impact on the growth of plants growing in
aromatic hydrocarbons), HCHs (hexachlorocyclohexane), PFASs contaminated soil. But presently our knowledge about this point is
(poly-fluoroalkyl substances), ethers, and fuel aromatics have been limited. Further research is required to prove whether MPs and
reported to be found on MPs in aquatic environments (Hüffer et al., sorbed chemicals are harmful to soil biota and plants or not?
2018; Wang and Wang, 2018; Zhan et al., 2016). A recent report has
shown that tetracycline antibiotics can make a complex with MPs 1.5. Effects on nutrient cycling
in the soil and can develop antibiotic resistance in microbial com-
munities (Ma et al., 2020). But further study is required to under- Plant growth and root development significantly depend upon
stand the occurrence and behaviour of heavy metals and organic the activity of microorganisms in the soil. Microorganisms play a
pollutants on MPs. pivotal role in the cycling of major nutrients through the decom-
MPs may increase the exposure of chemicals to soil-dwelling position of organic matter. Shifts in major functional processes in
organisms, microbes, and plants. These organic and inorganic the environment can affect microbial activities (Fig. 3, Table 2). MPs
compounds may adversely impact the growth of earthworms and are largely composed of carbon. Whether it is biodegradable or not,
other biotas in the soil (Fig. 2b, Table 2). Microorganisms and it will eventually release substantial amounts of carbon in the
earthworms both play a crucial role in enhancing the fertility of the environment (Rillig, 2018). The excess carbon can increase the
soil. Besides adding organic matter to the soil, earthworm’s growth of microbes through the build-up of new cells. But microbes
8
N. Khalid, M. Aqeel and A. Noman Environmental Pollution 267 (2020) 115653

also require other essential nutrients for their rising populations. (Lozano and Rillig, 2020) and could be big enough to be trans-
Hence, they may quench all those nutrients from the surrounding lated to plant community composition. These effects on plant
soil leaving a little bit or no nutrients for the plants. This could performance could have consequences for primary production and
negatively affect plant growth as a consequence of nutrient terrestrial ecosystem functioning. To achieve a more accurate
immobilization. Alterations in carbon to nitrogen ratios in the soil assessment of the effects of MPs on terrestrial systems and plants,
could also be possible (Qi et al., 2020), the results of which could research priorities and future directions are proposed in the
affect the whole plant community. Zhu et al. (2018b) reported a following:
significant reduction in the relative abundance of microbial families
Isosphaeraceae, Xanthobacteraceae, and Rhizobiaceae in the poly- 1. Monitoring programs are urgently required to assess the direct
styrene contaminated soil. These are key microbe families involved toxicity of microplastic pollutants in plants in various land set-
in organic matter decomposition and nitrogen cycling. Reproduc- tings. Furthermore, the mechanism of uptake, biological effects,
tion of key characters in the soil food web i.e. nematode (Caeno- and ecological risk assessment of MPs could be focused in future
rhabditis elegans) is also found to be severely affected by MPs that research. The increasing concentration of these anthropogenic
could impact the regulation of soil biogeochemical cycles (Scho € pfer particles could shift the baselines of physiological and
et al., 2020). ecosystem processes. These anthropogenic stressors may
Earthworms play an important role in the mineralization of already be imposing evolutionary pressure on some plant spe-
nutrients through the active incorporation of detritus into the cies. Therefore there is an urgent need to deal with this topic on
mineral soils (Marinissen and De Ruiter, 1993). They significantly a priority basis, and to provide sound information on the toxicity
add high concentrations of nutrients such as P, N, K, and Ca to the of microplastic pollutants on plants.
soil that is assimilated by plants easily. MPs adversely impact ac- 2. The effect of MPs on soil physicochemical properties further
tivities of earthworms in the soil. A handful of studies have revealed needed to be studied. Only a few studies have investigated the
the adverse effects of MPs on earthworms (Table 2). To better un- physical effects of MPs on the soil. This topic should be
derstand the effects of MPs on soil, biogeochemical processes expanded further taking into consideration a broad range of
should be taken into consideration because MPs are being entered MPs in different soil types. Biological impacts of soil aggregates
into the environment at an accelerated rate. formation by MPs and the effects of MPs have itself on microbial
communities by being enclosed in the soil aggregates should be
1.6. Thermal properties of microplastics: climate change below the taken into consideration. Additionally, it is known though that
ground MPs affect soil pH and EC, the mechanism of how this change
takes place, and the effects of altered soil pH and EC needed to
MPs can increase the temperature of the soil by absorbing solar be addressed. Because any change in these properties of soil
radiation. Plastics interact with solar radiation because of their could directly impact the growth of crop plants.
absorptivity, reflectivity, and transmittance. Because of these 3. MPs act as vectors and sinks of toxic organic and inorganic
properties, MPs can directly influence the microclimate of the crops pollutants in their surroundings. Chemicals released by them
in the root zone in the soil that can affect crop growth and yield. could be hazardous to soil-dwelling organisms and plants. Only
Higher soil temperatures increase activity and populations of soil a few studies have determined the effects of MPs on soil biota in
microorganisms, nutrient availability and uptake by roots, and the laboratory and controlled conditions. There is a tremendous
speedup seedling germination and growth (Farias-Larios et al., lack of knowledge on the effects of MPs on soil biota in the
1996). However, this would be beneficial only in cooler areas. The natural environment. To better understand the role of MPs in
heating properties of MPs may also cause severe problems for the the soil, their detailed effects on soil biota and plants are ur-
crop plants. Increased temperature in the microclimate in soil may gently needed to be studied. This includes their sorption and
promote evaporation and water loss. Researchers have already re- desorption mechanisms on MPs of different types and at varying
ported that high-zone temperature conditions in the soil created by levels of spatial and temporal scales in the soil. The role of MPs
plastics could be deleterious to the growth and yield of vegetables under the influence of these factors could be a topic for further
and highly dependent upon the plastic-type, crop species, time of research.
the year, and geographic location (Díaz-Pe rez and Batal, 2002; 4. Microorganisms play a vital role in biogeochemical cycling in
Ibarra-Jimenez and Zermeno-Gonzalez, 2008; Lamont, 2005). the rhizosphere. Roots of crops contain unique microfloral
communities and their interactions are crucial for crop growth
2. Conclusion and future recommendations and yield. The impact of MPs on microbial communities in the
root zone needed to be unveiled. As MPs are recognized to host
MPs are considered as emerging contaminants of concern. unique microorganisms on their surfaces different from the
Currently microplastic research has been focused on aquatic habi- surrounding environment in aquatic settings. But their role in
tats for almost a decade, however, terrestrial systems must be the the community development of certain microorganisms in the
main reservoirs of MPs because they first receive MPs from main soil remains unexplored. Also, the effect of MPs in the cycling of
sources on land. Nevertheless, the impacts of MPs distribution in various nutrients needed to be addressed.
terrestrial systems remain largely unexplored. This review dis- 5. The thermal properties of MPs in the root zone also needed to be
cusses various possibilities by which MPs could impact plants and emphasized. Various crop plants should be studied to explore
soil ecosystems. Only a limited number of studies conducted on the heating effect of different MPs types under various sets of
MPs and soils indicate that MPs have the potential to alter physi- environmental conditions to unravel the full extent of change in
cochemical characteristics of the soil. Which could impact plant terrestrial environments triggered by these pollutants.
growth and soil biota. Soil biota plays a tremendous role in regu-
lating the fertility of the soil but there is the uncertainty of
knowledge of the interaction between soil biota and MPs. MPs CRedit author statement
could also pose an additional threat to plants and soil biota by
releasing toxic contaminants to the environment. Changes in plant Noreen Khalid: Conceptualization, Writing - Original Draft.
growth and development caused by MPs are species-specific Muhammad Aqeel: Visualization, Writing - Review & Editing. Ali
9
N. Khalid, M. Aqeel and A. Noman Environmental Pollution 267 (2020) 115653

Noman: Writing - Review & Editing. Galloway, T.S., Cole, M., Lewis, C., 2017. Interactions of microplastic debris
throughout the marine ecosystem. Nat. Eco. Evol. 1, 1e8.
Hahladakis, J.N., Velis, C.A., Weber, R., Iacovidou, E., Purnell, P., 2018. An overview of
Declaration of competing interest chemical additives present in plastics: migration, release, fate and environ-
mental impact during their use, disposal and recycling. J. Hazard Mater. 344,
179e199.
The authors declare that they have no known competing Hodson, M.E., Duffus-Hodson, C.A., Clark, A., Prendergast-Miller, M.T., Thorpe, K.L.,
financial interests or personal relationships that could have 2017. Plastic bag derived-microplastics as a vector for metal exposure in
appeared to influence the work reported in this paper. terrestrial invertebrates. Environ. Sci. Technol. 51, 4714e4721.
Horton, A.A., Dixon, S.J., 2018. Microplastics: an introduction to environmental
transport processes. Wiley Interdisciplinary Reviews: Water 5, e1268.
References Huang, Y., Zhao, Y., Wang, J., Zhang, M., Jia, W., Qin, X., 2019. LDPE microplastic films
alter microbial community composition and enzymatic activities in soil. Envi-
Alimi, O.S., Farner Budarz, J., Hernandez, L.M., Tufenkji, N., 2018. Microplastics and ron. Pollut. 254, 112983.
nanoplastics in aquatic environments: aggregation, deposition, and enhanced Hüffer, T., Metzelder, F., Sigmund, G., Slawek, S., Schmidt, T.C., Hofmann, T., 2019.
contaminant transport. Environ. Sci. Technol. 52, 1704e1724. Polyethylene microplastics influence the transport of organic contaminants in
Awet, T., Kohl, Y., Meier, F., Straskraba, S., Grün, A.-L., Ruf, T., et al., 2018. Effects of soil. Sci. Total Environ. 657, 242e247.
polystyrene nanoparticles on the microbiota and functional diversity of en- Hüffer, T., Weniger, A.-K., Hofmann, T., 2018. Sorption of organic compounds by
zymes in soil. Environ. Sci. Eur. 30, 1e10. aged polystyrene microplastic particles. Environ. Pollut. 236, 218e225.
Bakir, A., O’Connor, I.A., Rowland, S.J., Hendriks, A.J., Thompson, R.C., 2016. Relative Ibarra-Jimenez, L., Zermeno-Gonzalez, A., 2008. Lozano-Del Rio J, Cedeno-Rubalcava
importance of microplastics as a pathway for the transfer of hydrophobic B, Ortega-Ortiz H. Changes in soil temperature, yield and photosynthetic
organic chemicals to marine life. Environ. Pollut. 219, 56e65. response of potato (Solanum tuberosum L.) under coloured plastic mulch.
Bandow, N., Will, V., Wachtendorf, V., Simon, F.-G., 2017. Contaminant release from Agrochimica 52, 263e272.
aged microplastic. Environ. Chem. 14, 394e405. Jiang, X., Chang, Y., Zhang, T., Qiao, Y., Klobu car, G., Li, M., 2020. Toxicological effects
Boots, B., Russell, C.W., Green, D.S., 2019. Effects of microplastics in soil ecosystems: of polystyrene microplastics on earthworm (Eisenia fetida). Environ. Pollut.
above and below ground. Environ. Sci. Technol. 53, 11496e11506. 259, 113896.
Bosker, T., Bouwman, L.J., Brun, N.R., Behrens, P., Vijver, M.G., 2019. Microplastics Jiang, X., Chen, H., Liao, Y., Ye, Z., Li, M., Klobu car, G., 2019. Ecotoxicity and geno-
accumulate on pores in seed capsule and delay germination and root growth of toxicity of polystyrene microplastics on higher plant Vicia faba. Environ. Pollut.
the terrestrial vascular plant Lepidium sativum. Chemosphere 226, 774e781. 250, 831e838.
Brennecke, D., Duarte, B., Paiva, F., Caçador, I., Canning-Clode, J., 2016. Microplastics Ju, H., Zhu, D., Qiao, M., 2019. Effects of polyethylene microplastics on the gut mi-
as vector for heavy metal contamination from the marine environment. Estuar. crobial community, reproduction and avoidance behaviors of the soil springtail,
Coast Shelf Sci. 178, 189e195. Folsomia candida. Environ. Pollut. 247, 890e897.
Brodhagen, M., Goldberger, J.R., Hayes, D.G., Inglis, D.A., Marsh, T.L., Miles, C., 2017. Judy, J.D., Williams, M., Gregg, A., Oliver, D., Kumar, A., Kookana, R., et al., 2019.
Policy considerations for limiting unintended residual plastic in agricultural Microplastics in municipal mixed-waste organic outputs induce minimal short
soils. Environ. Sci. Pol. 69, 81e84. to long-term toxicity in key terrestrial biota. Environ. Pollut. 252, 522e531.
Browne, M.A., 2015. Sources and Pathways of Microplastics to Habitats, Marine Kim, S.W., An, Y.-J., 2019. Soil microplastics inhibit the movement of springtail
Anthropogenic Litter. Springer, Cham, pp. 229e244. species. Environ. Int. 126, 699e706.
Browne, M.A., Galloway, T., Thompson, R., 2007. Microplastic-an emerging Kim, S.W., Kim, D., Chae, Y., Kim, D., An, Y.-J., 2019. Crop-dependent changes in
contaminant of potential concern? Integrated Environ. Assess. Manag. 3, water absorption of expanded polystyrene in soil environments. Chemosphere
559e561. 219, 345e350.
Chae, Y., An, Y.J., 2020. Nanoplastic ingestion induces behavioral disorders in Kwon, J.H., Chang, S., Hong, S.H., Shim, W.J., 2017. Microplastics as a vector of hy-
terrestrial snails: trophic transfer effects via vascular plants. Environ. Sci. J. drophobic contaminants: importance of hydrophobic additives. Integrated En-
Integr. Environ. Res.: Nano 7 (3), 975e983. viron. Assess. Manag. 13, 494e499.
Chai, B., Li, X., Liu, H., Lu, G., Dang, Z., Yin, H., 2020. Bacterial communities on soil Lahive, E., Walton, A., Horton, A.A., Spurgeon, D.J., Svendsen, C., 2019. Microplastic
microplastic at Guiyu, an E-Waste dismantling zone of China. Ecotoxicol. En- particles reduce reproduction in the terrestrial worm Enchytraeus crypticus in a
viron. Saf. 195, 110521. soil exposure. Environ. Pollut. 255, 113174.
Chen, H., Wang, Y., Sun, X., Peng, Y., Xiao, L., 2020a. Mixing effect of polylactic acid Lamont, W.J., 2005. Plastics: modifying the microclimate for the production of
microplastic and straw residue on soil property and ecological function. Che- vegetable crops. HortTechnology 15, 477e481.
mosphere 243, 125271. Lehmann, A., Fitschen, K., Rillig, M.C., 2019. Abiotic and biotic factors influencing the
Chen, Y., Liu, X., Leng, Y., Wang, J., 2020b. Defense responses in earthworms (Eisenia effect of microplastic on soil aggregation. Soil Systems 3, 21.
fetida) exposed to low-density polyethylene microplastics in soils. Ecotoxicol. Li, L., Luo, Y., Peijnenburg, W.J., Li, R., Yang, J., Zhou, Q., 2020. Confocal measurement
Environ. Saf. 187, 109788. of microplastics uptake by plants. Methods (Orlando) 7, 100750.
Cooper, D.A., Corcoran, P.L., 2010. Effects of mechanical and chemical processes on Li, L., Zhou, Q., Yin, N., Tu, C., Luo, Y., 2019. Uptake and accumulation of microplastics
the degradation of plastic beach debris on the island of Kauai. Hawaii. Mar. in an edible plant. Chin. Sci. Bull. 64, 928e934.
Pollut. Bull. 60, 650e654. Li, W.C., Tse, H., Fok, L., 2016. Plastic waste in the marine environment: a review of
Cole, M., Lindeque, P., Halsband, C., Galloway, T.S., 2011. Microplastics as contami- sources, occurrence and effects. Sci. Total Environ. 566, 333e349.
nants in the marine environment: a review. Mar. Pollut. Bull. 62, 2588e2597. Li, X., Chen, L., Mei, Q., Dong, B., Dai, X., Ding, G., et al., 2018. Microplastics in sewage
Corradini, F., Meza, P., Eguiluz, R., Casado, F., Huerta-Lwanga, E., Geissen, V., 2019. sludge from the wastewater treatment plants in China. Water Res. 142, 75e85.
Evidence of microplastic accumulation in agricultural soils from sewage sludge Liu, H., Yang, X., Liu, G., Liang, C., Xue, S., Chen, H., et al., 2017. Response of soil
disposal. Sci. Total Environ. 671, 411e420. dissolved organic matter to microplastic addition in Chinese loess soil. Che-
David, J., Steinmetz, Z., Kucerik, J.I., Schaumann, G.E., 2018. Quantitative analysis of mosphere 185, 907e917.
poly (ethylene terephthalate) microplastics in soil via thermogravimetryemass Liu, M., Lu, S., Song, Y., Lei, L., Hu, J., Lv, W., et al., 2018. Microplastic and mesoplastic
spectrometry. Anal. Chem. 90, 8793e8799. pollution in farmland soils in suburbs of Shanghai, China. Environ. Pollut 242,
De Falco, F., Gullo, M.P., Gentile, G., Di Pace, E., Cocca, M., Gelabert, L., et al., 2018. 855e862.
Evaluation of microplastic release caused by textile washing processes of syn- Lozano, Y.M., Rillig, M.C., 2020. Effects of microplastic fibers and drought on plant
thetic fabrics. Environ. Pollut. 236, 916e925. communities. Environ. Sci. Technol. 54 (10), 6166e6173. https://doi.org/
de Souza Machado, A.A., Kloas, W., Zarfl, C., Hempel, S., Rillig, M.C., 2018. Micro- 10.1021/acs.est.0c01051.
plastics as an emerging threat to terrestrial ecosystems. Global Change Biol. 24, Lwanga, E.H., Gertsen, H., Gooren, H., Peters, P., Sala nki, T., van der Ploeg, M., et al.,
1405e1416. 2017. Incorporation of microplastics from litter into burrows of Lumbricus ter-
Dehghani, S., Moore, F., Akhbarizadeh, R., 2017. Microplastic pollution in deposited restris. Environ. Pollut. 220, 523e531.
urban dust, Tehran metropolis. Iran. Environ. Sci. Pollut. Res. 24, 20360e20371. Ma, J., Sheng, G.D., O’Connor, P., 2020. Microplastics combined with tetracycline in
Díaz-Pe rez, J.C., Batal, K.D., 2002. Colored plastic film mulches affect tomato growth soils facilitate the formation of antibiotic resistance in the Enchytraeus crypticus
and yield via changes in root-zone temperature. J. Am. Soc. Hortic. Sci. 127, microbiome. Environ. Pollut. 114689.
127e135. Maaß, S., Daphi, D., Lehmann, A., Rillig, M.C., 2017. Transport of microplastics by two
Dong, Y., Gao, M., Song, Z., Qiu, W., 2020. Microplastic particles increase arsenic collembolan species. Environ. Pollut. 225, 456e459.
toxicity to rice seedlings. Environ. Pollut. 259, 113892. Mai, L., Bao, L.-J., Wong, C.S., Zeng, E.Y., 2018. Microplastics in the Terrestrial
Duis, K., Coors, A., 2016. Microplastics in the aquatic and terrestrial environment: Environment. Microplastic Contamination in Aquatic Environments. Elsevier,
sources (with a specific focus on personal care products), fate and effects. En- pp. 365e378.
viron. Sci. Eur. 28, 2. Marinissen, J., De Ruiter, P., 1993. Contribution of earthworms to carbon and ni-
Farias-Larios, J., Orozco, M., Guzman, S., Perez, J., 1996. Effect of plastic mulch, trogen cycling in agro-ecosystems. Agric. Ecosyst. Environ. 47, 59e74.
floating Rowcovers, and microtunnels on insect populations and yield of Napper, I.E., Bakir, A., Rowland, S.J., Thompson, R.C., 2015. Characterisation, quantity
muskmelon. Hortscience 31, 677b-677. and sorptive properties of microplastics extracted from cosmetics. Mar. Pollut.
Fei, Y., Huang, S., Zhang, H., Tong, Y., Wen, D., Xia, X., et al., 2020. Response of soil Bull. 99, 178e185.
enzyme activities and bacterial communities to the accumulation of micro- O’Connor, D., Pan, S., Shen, Z., Song, Y., Jin, Y., Wu, W.-M., et al., 2019. Microplastics
plastics in an acid cropped soil. Sci. Total Environ. 707, 135634. undergo accelerated vertical migration in sand soil due to small size and wet-

̌ ́ 10
N. Khalid, M. Aqeel and A. Noman Environmental Pollution 267 (2020) 115653

dry cycles. Environ. Pollut. 249, 527e534. Wan, Y., Wu, C., Xue, Q., Hui, X., 2019. Effects of plastic contamination on water
Pignattelli, S., Broccoli, A., Renzi, M., 2020. Physiological responses of garden cress evaporation and desiccation cracking in soil. Sci. Total Environ. 654, 576e582.
(L. sativum) to different types of microplastics. Sci. Total Environ 138609. Wang, F., Zhang, X., Zhang, S., Zhang, S., Sun, Y., 2020. Interactions of microplastics
Powell, J.R., Rillig, M.C., 2018. Biodiversity of arbuscular mycorrhizal fungi and and cadmium on plant growth and arbuscular mycorrhizal fungal communities
ecosystem function. New Phytol. 220, 1059e1075. in an agricultural soil. Chemosphere 126791.
Prendergast-Miller, M.T., Katsiamides, A., Abbass, M., Sturzenbaum, S.R., Wang, H.-T., Ding, J., Xiong, C., Zhu, D., Li, G., Jia, X.-Y., et al., 2019a. Exposure to
Thorpe, K.L., Hodson, M.E., 2019. Polyester-derived microfibre impacts on the microplastics lowers arsenic accumulation and alters gut bacterial communities
soil-dwelling earthworm Lumbricus terrestris. Environ. Pollut. 251, 453e459. of earthworm Metaphire californica. Environ. Pollut. 251, 110e116.
Qi, Y., Ossowicki, A., Yang, X., Lwanga, E.H., Dini-Andreote, F., Geissen, V., et al., 2020. Wang, J., Coffin, S., Sun, C., Schlenk, D., Gan, J., 2019b. Negligible effects of micro-
Effects of plastic mulch film residues on wheat rhizosphere and soil properties. plastics on animal fitness and HOC bioaccumulation in earthworm Eisenia fetida
J. Hazard Mater. 387, 121711. in soil. Environ. Pollut. 249, 776e784.
Qi, Y., Yang, X., Pelaez, A.M., Lwanga, E.H., Beriot, N., Gertsen, H., et al., 2018. Macro- Wang, J., Liu, X., Li, Y., Powell, T., Wang, X., Wang, G., Zhang, P., 2019c. Microplastics
and micro-plastics in soil-plant system: effects of plastic mulch film residues on as contaminants in the soil environment: a mini-review. Sci. Total Environ. 691,
wheat (Triticum aestivum) growth. Sci. Total Environ. 645, 1048e1056. 848e857.
Rillig, M.C., 2012. Microplastic in terrestrial ecosystems and the soil? Environ. Sci. Wang, W., Wang, J., 2018. Comparative evaluation of sorption kinetics and iso-
Tchnol. 46 (12), 6453e6454. therms of pyrene onto microplastics. Chemosphere 193, 567e573.
Rillig, M.C., 2018. Microplastic disguising as soil carbon storage. Environ. Sci. Watteau, F., Dignac, M.-F., Bouchard, A., Revallier, A., Houot, S., 2018. Microplastic
Technol. 52 (11), 6079e6080. detection in soil amended with municipal solid waste composts as revealed by
Rillig, M.C., Bonkowski, M., 2018. Microplastic and soil protists: a call for research. transmission electronic microscopy and pyrolysis/GC/MS. Front. Sustain. Food
Environ. Pollut. 241, 1128e1131. Syst 2, 81.
Rillig, M.C., Ryo, M., Lehmann, A., Aguilar-Trigueros, C.A., Buchert, S., Wulf, A., et al., Xu, B., Liu, F., Cryder, Z., Huang, D., Lu, Z., He, Y., Wang, H., Lu, Z., Brookes, P.C.,
2019. The role of multiple global change factors in driving soil functions and Tang, C., Gan, J., 2019. Microplastics in the soil environment: occurrence, risks,
microbial biodiversity. Science 366, 886e890. interactions and fateeA review. Critical Rev. Environ. Sci. Technol. 1e48.
Rillig, M.C., Ziersch, L., Hempel, S., 2017. Microplastic transport in soil by earth- Yang, X., Bento, C.P., Chen, H., Zhang, H., Xue, S., Lwanga, E.H., et al., 2018. Influence
worms. Sci. For. Rep. 7. of microplastic addition on glyphosate decay and soil microbial activities in
Rodríguez-Seijo, A., da Costa, J.P., Rocha-Santos, T., Duarte, A.C., Pereira, R., 2018. Chinese loess soil. Environ. Pollut. 242, 338e347.
Oxidative stress, energy metabolism and molecular responses of earthworms Yi, M., Zhou, S., Zhang, L., Ding, S., 2020. The effects of three different microplastics
(Eisenia fetida) exposed to low-density polyethylene microplastics. Environ. Sci. on enzyme activities and microbial communities in soil. Water Environ. Res.
Pollut. Res. 25, 33599e33610. https://doi.org/10.1002/wer.1327.
Rodriguez-Seijo, A., Lourenço, J., Rocha-Santos, T., Da Costa, J., Duarte, A., Vala, H., Yu, M., Van Der Ploeg, M., Lwanga, E.H., Yang, X., Zhang, S., Ma, X., et al., 2019.
et al., 2017. Histopathological and molecular effects of microplastics in Eisenia Leaching of microplastics by preferential flow in earthworm (Lumbricus ter-
andrei Bouche . Environ. Pollut. 220, 495e503. restris) burrows. Environ. Chem. 16, 31e40.
Rodríguez-Seijo, A., Santos, B., da Silva, E.F., Cachada, A., Pereira, R., 2019. Low- Zhan, Z., Wang, J., Peng, J., Xie, Q., Huang, Y., Gao, Y., 2016. Sorption of 3, 30 , 4, 40 -
density polyethylene microplastics as a source and carriers of agrochemicals to tetrachlorobiphenyl by microplastics: a case study of polypropylene. Mar. Pol-
soil and earthworms. Environ. Chem. 16, 8e17. lut. Bull. 110, 559e563.
Rousk, J., Brookes, P.C., Bååth, E., 2009. Contrasting soil pH effects on fungal and Zhang, G., Liu, Y., 2018. The distribution of microplastics in soil aggregate fractions
bacterial growth suggest functional redundancy in carbon mineralization. Appl. in southwestern. China. Sci. Total Environ 642, 12e20.
Environ. Microbiol. 75, 1589e1596. Zhang, M., Zhao, Y., Qin, X., Jia, W., Chai, L., Huang, M., et al., 2019. Microplastics
Rychter, P., Christova, D., Lewicka, K., Rogacz, D., 2019. Ecotoxicological impact of from mulching film is a distinct habitat for bacteria in farmland soil. Sci. Total
selected polyethylenimines toward their potential application as nitrogen fer- Environ. 688, 470e478.
tilizers with prolonged activity. Chemosphere 226, 800e808. Zhou, Y., Liu, X., Wang, J., 2019. Characterization of microplastics and the association
Scheurer, M., Bigalke, M., 2018. Microplastics in Swiss floodplain soils. Environ. Sci. of heavy metals with microplastics in suburban soil of central. China. Sci. Total
Technol. 52 (6), 3591e3598. Environ 694, 133798.
Scho€ pfer, L., Menzel, R., Schnepf, U., Ruess, L., Marhan, S., Brümmer, F., et al., 2020. Zhou, Y., Liu, X., Wang, J., 2020. Ecotoxicological effects of microplastics and cad-
Microplastics effects on reproduction and body length of the soil-dwelling mium on the earthworm Eisenia foetida. J. Hazard Mater. 392, 122273.
nematode Caenorhabditis elegans. Front. Envrion. Sci. 8, 41. Zhu, B.-K., Fang, Y.-M., Zhu, D., Christie, P., Ke, X., Zhu, Y.-G., 2018a. Exposure to
Song, Y., Cao, C., Qiu, R., Hu, J., Liu, M., Lu, S., et al., 2019. Uptake and adverse effects nanoplastics disturbs the gut microbiome in the soil oligochaete Enchytraeus
of polyethylene terephthalate microplastics fibers on terrestrial snails (Achatina crypticus. Environ. Pollut. 239, 408e415.
fulica) after soil exposure. Environ. Pollut. 250, 447e455. Zhu, D., Bi, Q.-F., Xiang, Q., Chen, Q.-L., Christie, P., Ke, X., et al., 2018b. Trophic
Sun, J., Dai, X., Wang, Q., van Loosdrecht, M.C., Ni, B.-J., 2019. Microplastics in predator-prey relationships promote transport of microplastics compared with
wastewater treatment plants: detection, occurrence and removal. Water Res. the single Hypoaspis aculeifer and Folsomia candida. Environ. Pollut. 235,
152, 21e37. 150e154.
Su, L., Nan, B., Craig, N.J., Pettigrove, V., 2020. Temporal and spatial variations of Zhu, D., Chen, Q.-L., An, X.-L., Yang, X.-R., Christie, P., Ke, X., et al., 2018c. Exposure of
microplastics in roadside dust from rural and urban Victoria, Australia: impli- soil collembolans to microplastics perturbs their gut microbiota and alters their
cations for diffuse pollution. Chemosphere 126567. isotopic composition. Soil Biol. Biochem. 116, 302e310.

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