3.1. Distribution of microplastic in water and sediment samples: According to the data based on (Table S1) the water quality of urban lakes is poor, but the condition of Gulshan Lake is worse than the other lakes. The Dissolve Oxygen (DO), Electrical conductivity (EC), Turbidity is higher than the permissible limit. As well, the presence of microplastic debris was identified in all the water and sediment samples (Table S2) of urban lakes. In water samples, microplastic abundance varied from 0-9 items/L. Highest abundance of microplastic was observed in Gulshan Lake (0-9 items/L), followed by Hatir Jheel Lake (0-8 items/L), and comparatively low abundance of microplastic was observed in Dhanmondi Lake (0-4 items/L). In sediment samples, abundance varied from (0-16 items/kg). The abundance of microplastic was highest in Gulshan Lake (0-16 items/kg), followed by Hatir Jheel Lake (0-11 items/kg), and comparatively low abundance of microplastic was observed in Dhanmondi Lake (0-9 items/kg).
The morphotypes of identified microplastic particles were: (a) Fiber (uniform plastic strands); (b) Fiber (fibrous); (c) Fragments (hard); (d) Fragments (jagged-edged); (e) Micro-pellets (hard, rounded particles); (f) Films (2-dimensional plastic films) (h) Foam (Styrofoam material).
The dominant morphotypes were identified for all environmental samples. In water samples, the prominent types of microplastic were film (40.91%), followed by micro pellets (36.36%), fragment (22.73%), and fiber (13.63%). In sediment samples, film was the most abundant type of microplastic, accounted for about 33.33%. There was also fiber (30.55%), fragment (27.77%), micro pellets (2.77%) and foam (2.77%). The most dominant polymer was film, found almost in every sample. Two types of fibers were found in the samples (fibrous and uniform plastic strand). Between them fibrous fibers were the prominent one.
In water samples, from 20 items a representative number of particles (n=5) were selected and confirmed as plastic particles with FTIR analysis. The detected polymer types were High-density polyethylene (HDPE), Polyvinyl chloride (PVC), Polycarbonate (PC). The dominant type was HDPE accounting for 60%, followed by PVC 20%, PC 20%.
In sediment samples, from 36 items a representative number of particles (n=7) were selected and confirmed as plastic particles with FTIR. The detected polymer types were High-density polyethylene (HDPE), Cellulose acetate (CA), Polycarbonate (PC), Polypropylene (PP). The most abundant polymer was HDPE, which accounted for 42.85%, followed by PC 28.57%, CA 14.28%, and PP 14.28%.
Table 1: Abundance of MPs in fish samples from each lake
Site
|
Species
|
Items/individual
|
Items/gm (GIT)
|
Dominent morphotype
|
Dhanmondi Lake
|
Channa marulius
|
0-7
|
0-0.31
|
Foam
|
Channa punctate
|
0-1
|
0-0.60
|
Film
|
Chitala chitala
|
0-11
|
0-2.30
|
Micro-pellet
|
Oreochromis mossambicus
|
0-17
|
0-4.88
|
Micro-pellet
|
Catla catla
|
0-2
|
0-0.11
|
Foam
|
Gulshan Lake
|
Pangasius pangasius
|
0-2
|
0-1.2
|
Fragment
|
Hatir Jheel lake
|
Pangasius pangasius
|
0-2
|
0-0.13
|
Micro-pellet
|
Channa striata
|
0-7
|
0-1.23
|
Foam
|
Catla catla
|
0-15
|
0-1.40
|
Micro-pellet
|
3.2. Distribution of microplastic in fish samples:
Microplastic abundance was observed in all the fish samples (Table S2) and microplastics were found in almost all the samples after digestion. Based on the data from (Table 1), the highest abundance of microplastic observed in an individual fish was in Oreochromis mossambicus from Dhanmondi Lake, showing the presence of 0-17 items/individual, 0-4.88 items/g in the GIT, followed by Catla catla from Hatir Jheel Lake containing 0-15 items/individual, 0-1.40 items/g in the GIT. A comparatively low abundance of microplastic was observed Pangasius pangasius in Gulshan Lake where 0-2 items/ individual, 0-1.2 items/g in the GIT were present. The percentage of dominant type was identified for all the fish samples. A prominent type of microplastic in fish samples were micro pellets 29.28%, followed by foams 27.85%, film 24.28%, fragment 17.28%, and fiber 13.63%. However, plastic films were prevailing in water and sediment samples, whereas micro pellets were dominant in fish samples. In fish samples, from 81 items a representative number of particles (n=10) were selected and confirmed as plastic particles with FTIR. The polymer types were High-density polyethylene (HDPE), Polyvinyl chloride (PVC), Polycarbonate (PC), Polypropylene (PP), Ethylene vinyl acetate (EVA) and 1 remain unidentified. The dominant polymer was HDPE accounted for 40% followed by PVC 30%, PC 10%, EVA 10%, PP 10%.
3.3. Factors influencing MPs uptake by fish sample: There is a significant possibility of MPs ingestion among large fishes as they need high energy resulting in high food intake. Several studies investigated and observed MPs accumulation have significant positive correlations with length/body weight of fish (Horton et al., 2018; Hossain et al., 2019). The goal of this study was to observe if MP intake differs as body weight and length of a fish species varies. Though, no significant correlations between microplastic abundance and fish body weight/length (R²= 0.0156-0.0340, p>0.4) were found (Figure 4).
As a result of the above observation, it can be assumed that the abundance of MPs in fish is not proportional to body length or weight, rather it is dependent to the intensity of plastic pollution in the surrounding environment. It was also observed by Carbery et al. (2018) that environmental plastic abundance affects MPs intake by fish. However, due to the small sample size significant correlations between MPs abundance and fish body weight/length may be obscured.
3.4. Identification of potential MPs using FTIR technique:
From each morphotype a representative number of microplastics were selected for FTIR verifications out of 138 particles. Particles were carefully cleaned and dried before being analyzed to remove organic debris. A total 17 particles were selected for verification and failed to verify particles were considered as non-plastic material to ensure validity of result. From 17 particles 16 were confirmed as plastic while 1 considered non-plastic material. The primary polymer types detected based on characteristic peak from FTIR analysis (Figure S3) are High density polyethylene (HDPE), Polyvinyl chloride (PVC), Polycarbonate (PC), Ethylene Vinyl Acetate (EVA), Cellulose Acetate (CA), and Polypropylene (PP) (Noda et al., 2007; Krehula et al., 2014; Jung et al., 2018). The composition of these polymers are as follows: HDPE (5 particles), EVA (3 particles), PVC (3 particles), PC (2 particles), PP (2 particles), CA (1 particle).
The IR spectrum based on adsorption band (cm-1) of the corresponding particles are shown in Figure 5. In contrast to the reference polymer spectra, spectrum (a) shows the characteristic peak for HDPE assigned to CH2 Asymmetric C-H stretching at peak 2916.37 cm-1 and CH2 Symmetric C-H stretching at peak 2848.86 cm-1; CH2 bend stretching at peak 1739.79 cm-1, 1469.76 cm-1, 1456.26 cm-1; CH2 rock stretching at 719.24 cm-1 and C(=O)O stretching at peak 667.37 cm-1 (Jung et al., 2018).
In contrast to the reference polymer spectra, spectrum (b) shows the characteristic peaks for PVC are assigned to Aromatic CH in plane bending at peak 1170.79 cm-1; C=C stretching at peak 1099.43 cm-1 and 1033.85 cm-1; C-Cl stretching at peak 601.79 cm-1 and 557.43 cm-1 (Jung et al., 2018).
Spectrum (c) exhibits the distinctive peaks for EVA are assigned to CH2 Asymmetric C-H stretching at peak 2950.83 cm-1 and CH2 Symmetric C-H stretching at peak 2895.70 cm-1; C=O stretching peak at 1741.72 cm-1; CH2 bending at peak 1535.97 cm-1 and 1460.784 cm-1; C(=O)O stretching at peak 1166.581 cm-1; C-O stretching at peak 1097.953 cm-1; CH2 rocking at peak 721.639 cm-1 (Jung et al., 2018).
Spectrum (d) shows the characteristic peak for PC were found at absorption band 2923.35 cm-1,1740.34 cm-1, 1433.3401 cm-1, 1409.58 cm-1, 972.65 cm-1, 838.59 cm-1. The absorption bands indicate the presence of CH stretching at peak 2923.35 cm-1; C=O stretching at peak 1740.34 cm-1 and 1409.58 cm-1; Aromatic ring stretching at peak 1433.3401 cm-1; Aromatic CH in plane bending at 972.65 cm-1, 838.59 cm-1 (Jung et al., 2018).
Spectrum (e) shows the distinctive peaks for CA are ascribed to C=O stretching at peak 1716.010 cm-1; CH3 bending at peak 1247.672 cm-1; CH bending at peak 1015.652 cm-1; O-H bending at peak 724.092 cm-1 (Jung et al., 2018).
Spectrum (f) shows the characteristic peak for PP were found at absorption band 2850.639 cm-1,1741.316 cm-1, 1462.246 cm-1, 1166.54 cm-1, 1029.226 cm-1, 878.94 cm-1 and 769.18 cm-1. The absorption bands indicate the presence of C-H stretching at peak 2850.639 cm-1; CH2 bending at peak 1741.316 cm-1; CH3 bending at peak 1462.246 cm-1; CH bending at peak 1166.54 cm-1 and 1029.226 cm-1; CH2 rocking at peak 878.94 cm-1 and 769.18 cm-1 (Jung et al., 2018).