Introduction

In recent years, marine environments have been well studied regarding microplastic (MP) pollution; however, the knowledge about freshwater biota affected by MPs remains insufficient (de Sá et al. 2018; Lambert and Wagner 2018). Several studies have focused on fish and invertebrates in freshwaters, mainly concerned river and lake ecosystems (Roch et al. 2019; Windsor et al. 2019). In contrast, the available data is scarce on MPs in small water bodies and animals living therein (Hu et al. 2018; Li et al. 2018; Roch et al. 2019). Amphibians constitute an important part of freshwater food webs, and they are considered the most endangered group of vertebrates worldwide (Stuart et al. 2004). Due to the growing problem of their global extinction, it is important to detect and monitor potential threats for this group. Although many studies confirmed negative effect of other contaminants (e.g. atrazine, estrogen, plasticizer bisphenol A, etc.) on amphibian development, both in situ or under laboratory conditions (Hayes et al. 2010; Tamschick et al. 2016; Lambert et al. 2015), they remain one of the least studied animals in the context of MP contamination (de Sá et al. 2018). It is thus important to assess whether MPs constitute an important threat to wild amphibians. Hitherto, four reports focused on the accumulation and potential effect of polystyrene MPs on Xenopus spp. and Alytes obstetricans tadpoles and polyethylene MPs on Physalaemus cuvieri tadpoles under experimental conditions (Hu et al. 2016; De Felice et al. 2018; Boyero et al. 2020; da Costa Araújo et al. 2020). Additionally, only Hu et al. (2018) detected MPs in tadpoles from small water bodies around the Yangtze River Delta in China and Iannella et al. (2020) found plastic items in stomach content of Triturus carnifex living in livestock’s watering points in Italy.

So far, only few reports have documented the occurrence of MPs in Central European river fauna (e.g. Roch et al. 2019; Kuśmierek and Popiołek 2020), and only Roch et al. (2019) and Bordós et al. (2019) focused on lakes and fish ponds. In this study, we aimed to examine the occurrence and chemical composition of MPs in tadpoles of pond-breeding amphibians from Poland, Central Europe. Recent study showed that fish length as well as urbanisation process influences MP ingestion (Peters and Bratton 2016); thus, we also checked whether there are differences between number of tadpoles with MPs that occur in urban and surrounding area and whether tadpoles body size increases the probability of MP ingestion.

Materials and methods

The study was conducted from May to June, in 2017 and 2018, in southwestern Poland. Material was collected in ponds situated in (i) urban green spaces of the Wrocław city and (ii) surrounding areas covered mostly by fields, small forest patches and villages. Tadpoles were caught using a herpetological net, then euthanised in MS-222, measured (SVL, mm) and identified to the species level with the key described by Berger (2000). MP extraction followed protocols previously described by Kuśmierek and Popiołek (2020) and Hu et al. (2018) with some modifications. Whole tadpole bodies were then washed with distilled water. They were subsequently flooded with 30% hydrogen peroxide (H2O2; followed by Mathalon and Hill 2014), incubated at 60 °C for 4 h in a glass beaker, and MPs were then searched for by means of a stereomicroscope (Zeiss Stemi SV11). To avoid contamination, a cotton laboratory coat was worn during procedures, and prior to use, all liquids (pure water and H2O2) were filtered using filter paper (5-μm porosity) as well as the equipment used during procedures was rinsed in pure water.

Qualitative microplastic analysis was performed with infrared spectroscopy with the use of an IR Affinity-1S Shimadzu equipped with the Specac Quest ATR. The absorbance measurements were made at a wavelength range of 600–4200 cm−1. The obtained spectra were analysed by the HYPER-IR Library (ATR samples library). The average similarity between the received spectrum and the library spectra was over 70%. It should be noted that some particles were lost due to their small size and could not be analysed.

Statistical analysis was performed using Statistica 13.1 software (StatSoft, Poland). We used the Spearman rank order correlation to determine the correlation between the number of MPs and tadpole body length. We also used 2 × 2 contingency tables and Fisher’s exact tests to compare the proportion of common toad Bufo bufo tadpoles which ingested MPs from the city and surrounding areas.

Results

In total, 201 tadpoles of 5 species (common toad Bufo bufo, common frog Rana temporaria, water frogs Pelophylax esculentus complex, spadefoot toad Pelobates fuscus and tree frog Hyla arborea) were collected from 8 ponds, of which 3 were located in the city of Wrocław and 5 in areas from the surroundings of city (Table 1). MPs were found in all studied sites and in all studied species (Table 1). Of all, 53 (26%) tadpoles ingested a total of 71 MPs (mean 0.35, SD 0.7). There was no correlation between tadpole SVL and the number of ingested MPs (Spearman correlation r = 0.07, p = 0.34) and no significant differences between the number of common toad tadpoles from the city and rural areas that ingested MPs (p = 0.2).

Table 1 Microplastic detection in sampling sites representing the studied populations of five amphibian species

The majority of particles were fibres (69 items, equalling 97%; Fig. 1) followed by two fragments (3%). The mean length of fibres reached 2.2 mm SD 1.3, and the dimensions of the fragments were 0.5 × 1 and 0.5 × 0.2 mm. The colours of MPs detected were diverse (transparent, blue, navy blue, black, brown, red, violet and pink).

Fig. 1
figure 1

Examples of MPs found in tadpoles

Spectroscopy analysis revealed that particles (N = 53) were of anthropogenic origin and included nylon (amorphous nylon, nylon 6/12, nylon 12/polyamide, nylon mxd6; 90%), polyisoprene (6%), polyurethane (2%) and 1,2 polybutadiene (2%) (Fig. 2).

Fig. 2
figure 2

IR-ATR spectra obtained from isolated MPs and their possible origin

Discussion

The results of this study are in line with other reports that have shown the occurrence of MPs in various kinds of European inland waters, including: large and small rivers (e.g. Horton et al. 2018; Roch et al. 2019; Slootmaekers et al. 2019), fish ponds (Bordós et al. 2019) and lakes (Faure et al. 2012; Roch et al. 2019). So far, small water bodies have been one of the least studied aquatic ecosystems in the context of MPs; however, they play key ecological role globally, contributing to the maintenance of biogeochemical cycles and freshwater biodiversity (Biggs et al. 2017). Further research should therefore focus on the accumulation and potential effects of plastic particles on biota that inhabit therein (Hu et al. 2018).

We confirmed that tadpoles of pond-breeding amphibians which live in Central Europe are exposed to MP pollution. However, the mean number of MP per individual was lower than in tadpoles from the small water bodies of Yangtze River Delta in China (Hu et al. 2018). It should be emphasised that those ponds are situated around a river estuary and can therefore accumulate MPs which flow from upriver. Recent laboratory experiments revealed that MPs accumulate in the gills and digestive tracts of tadpoles; however, their elimination is relatively fast (Hu et al. 2016; De Felice et al. 2018). Moreover, ingestion of MPs is higher along with higher MP concentrations, but food availability decreases absorption and increases the elimination of MPs (Hu et al. 2016).

Experimental studies showed that although MP concentrations of 12.5 μg mL−1 (Ø = 3 μm) did not affect body growth or the swimming activity of tadpoles (De Felice et al. 2018), exposure at 60 mg/L for the time of 7 days (mean diameter ca. 35.5 μm) led to mutagenic effect (da Costa Araújo et al. 2020), and after exposure to 1800 MPs mL−1 (Ø = 10 μm), most tadpoles died (Boyero et al. 2020). However, a low mean number of MPs in tadpoles from our study should not influence the development of tadpoles. It should be emphasised that in both experiments, only very small particles were used. As we found fibres that were as large as even 5 mm in size, further investigation should be planned in order to assess the potential effect of such particles on the digestive tract (i.e. intestinal injures).

So far, polyethylene, polystyrene, polypropylene and polyester were considered as the most common types of MPs detected in aquatic organisms (de Sá et al. 2018). Surprisingly, none of these were found in our study. Their total absence may be caused by the small sample size (i.e. low number of analysed fibres). Instead of these typical examples of MPs, we found other types which are less common. Nylon, the most abundant in our sample, is commonly applied in textiles (e.g. clothes), plastic machine parts (e.g. in electronics), films for packing material in the food industry, and in the production of monofilaments, seat belts, automotive airbags, tarpaulins, ropes, nets and other products. Laundry wastewater or intensive fishing activities may be considered as a source of this polymer in the environment (Naji et al. 2017; Yuan et al. 2019). Interestingly, we found a few fibres of polyisoprene and 1,2 polybutadiene in two ponds. Both polymers are used in the production of tyres, so we supposed that the source of these MPs was from tire abrasion on the road nearby both ponds.

In conclusion, to our knowledge, this is a first report showing MP ingestion by tadpoles living in water bodies in Central Europe. It suggests that they can be a significant vector of MP transfer from aquatic to terrestrial environments. The small number of particles per individual may suggest a low impact on these organisms. However, regarding disturbing results obtained under laboratory conditions, further research on the impact of MPs on tadpole growth and survival should be continued in situ.