Abstract
The result presented in this chapter underlines for the first time the occurrence of plastic waste in the stomachs of Sea of Oman lanternfishes (Myctophidae), Benthosema fibulatum (Gilbert and Cramer 1897) and Benthosema pterotum (Alcock 1890). Fish samples were obtained from the coasts of Muscat city at the Sea of Oman. Plastic fragments consumed were grouped into small microplastics (0.2–2 mm), large microplastics (2–5 mm) and mesoplastics (5–25 mm), chiefly with clear colours. A higher number of plastics were obtained from the stomach of B. pterotum (20), while 15 pieces were collected from the stomach of B. fibulatum. The plastic intake could lead to severe effects especially the vertical migratory lanternfishes. Ecotoxicological features related to the possible influences of pollutants on lanternfish biology and to the mobilization of contaminants throughout the marine nourishing level up to top predators should be intensified if the management of plastic in the sea is not very well controlled.
Access provided by Autonomous University of Puebla. Download chapter PDF
Similar content being viewed by others
Keywords
1 Introduction
The majority of the marine wastes are plastic. The issue of marine debris has been recognized internationally as a source of harmful influences on the marine organisms (Derraik 2002). Plastic debris can be classified into large, medium and small. The large plastic objects can produce tangle and can be swallowed by organisms. The medium plastic pieces can harm organisms during the respiration, ingestion processes and can lead to a gastric blockade, physiological influences, chemical transfer, or nourishing changes (Lusher et al. 2015). The small fragments of plastic, which are also known as microplastic, are usually taken by organisms easy with its food, or they were misguided being foodstuffs (DeWitte et al. 2014; Romeo et al. 2016). The smaller fragments of plastic are usually observed in the stomach of several fish including the commercially important species (Lusher et al. 2015; Boerger et al. 2010; Romeo et al. 2016).
The feeding habit of the mesopelagic fish species includes remaining during the day time at certain depth in the water column just below the photic zone, and then they start feeding on the zooplankton near the surface of the water after making a vertical migration (Clark and Levy 1988). Microplastics are usually intermingled with the preferred food items of the mesopelagic fishes and create a good possibility for the fish to intake them with the food (Lusher 2015), and it is possible to be conveyed to larger marine animals including large piscivorous fishes and different marine mammals.
The results presented in this chapter are about the first-time incident of plastic remains in the stomach contents of two Sea of Oman mesopelagic fishes belonging to the family of Myctophidae (lanternfishes): the skinnycheek lanternfish Benthosema pterotum (Alcock 1890) (Romeo et al. 2016) and the spinycheek lanternfish Benthosema fibulatum (Gilbert and Cramer 1897) (Romeo et al. 2016). Due to the vital role of lanternfishes in the trophic web in the sea, the information given in the present chapter will be a significant addition to those already present on the occurrence of plastic in the digestive tract of the myctophid fish species.
2 The Lanternfish Species Studied
2.1 Spinycheek Lanternfish Benthosema fibulatum (Gilbert and Cramer 1897)
Marine species lives in the bathypelagic region of the sea (Riede 2004) at depth range 0–2000 m (Weitkamp and Sullivan 2003). Individuals of this species are found dispersed in both the Indian and the Pacific oceans. Maximum length reached is 100 mm in total length (Paxton and Hulley 1999). Individuals infrequently visit slop areas especially during the dark nights. Allured by light like insects, shown to be unsettled and dashing hysterically in all directions (Kuiter and Tonozuka 2001).
2.2 Skinnycheek Lanternfish Benthosema pterotum (Alcock 1890)
A marine species living in the benthopelagic region of the sea at depth range 100–300 m (Hulley 1986). Individuals of this species are widely dispersed in the Indo-Pacific zone from off Mozambique to the Sea of Oman and eastward to the Bay of Bengal, Indonesia and Western Australia and north of Japan (Olivar et al. 1999). It attains a maximum size of 70 mm in total length (Paxton and Hulley 1999). It feeds mainly on copepods and various crustacean larvae (Gjøsaeter and Kawaguchi 1980).
3 Materials Obtained and Processed
Specimens of lanternfish were obtained by midwater trawler operating off shorelines of Muscat city on the Sea of Oman. Specimens were cleaned by washing them with tap water and wrapped in aluminium foil to circumvent external contamination. A total of 120 B. fibulatum and 150 B. pterotum were collected. Specimens were preserved frozen at −20 °C. Body measurements and weight were taken for each specimen. To examine the food intake by the fish, the stomach was removed and examined in the laboratory. Conferring to Lusher et al. (2015), all tools and gear used were washed and proved clean of any airborne plastic fibre using a light microscope. Plastic fragments were counted, weighed and measured (length, width, thickness) and characterized by the stereomicroscope Zeiss Discovery V.8. Bestowing to Galgani et al. (2013), plastics ingested were classified into microplastics (<5 mm) and mesoplastics (5–25 mm). Furthermore, the microplastics were in turn sorted as small microplastics (0.2–2 mm) and large microplastics (2–5 mm), as described by Collignon et al. (2014).
4 Data Analysis
The data analysis followed that of Romeo et al. (2016). In total, 35 plastic pieces were located in the stomach content of the two lanternfishes (15 in B. fibulatum and 20 in B. pterotum) (Table 1). The mean values and range of fish standard length (mm) and weight (g) in addition to the number of plastics retrieved for each species are shown in Table 1.
The results showed that there is a slight variation in the shape of the plastic fragments from irregular to rectangular, round or elongated, and the most part of them was flat. Several colours of pieces of plastic were perceived, with light colours which were prevailing. In both lanternfish species, the hyaline and white plastics were the most frequent (41% and 36%, respectively).
Table 2 showing the incidence of existence, colour and size (mean values, range and standard deviation values) of plastic bits were obtained from the stomach substances of the two species of lanternfishes examined.
Fragments of small microplastics representing the majority of plastic material in the stomach of the lanternfishes were studied and showed variation in their number, while big microplastics were detected in equal fraction in the stomachs of B. fibulatum and 20 in B. pterotum, while mesoplastics were only found in the stomachs of B. fibulatum.
5 Remarks
Results given in this chapter are the first-time consumption of plastic fragments in Sea of Oman mesopelagic fish, belonging to the family of Myctophidae. While such species have no profitable value for fishery purposes, they have an enormous biomass and are important constituents in the marine nourishment cycle (Gjøsaeter and Kawaguchi 1980; Romeo et al. 2016). Certainly they are intricate in the transferal of energy from zooplankton to upper nourishment cycle and from epipelagic to deep waters (several lanternfish usually accomplish diel vertical movements) (Gjøsaeter and Kawaguchi 1980). Many pelagic top predators feed on lanternfishes (e.g. Springer et al. 1999; Moteki et al. 2001; Romeo et al. 2016). The problem of ingestion of plastic by lanternfish is a dilemma to their predators as the plastic debris may form a supplier of impurities which could decide bioaccumulation phenomena. Definitely, while the occurrence of plastics consumed is not high, lanternfish are often eaten by large fish (Karakulak et al. 2009; Battaglia et al. 2013; Romeo et al. 2016), which feed on their groupings, consuming a big number of individuals (Battaglia et al. 2013). This type of feeding could expand the incidence of microplastic in this top predator.
Reports on the presence of plastic consumption by mesopelagic fishes are available from different parts of the world, e.g. in the Pacific Ocean (Boerger et al. 2010; Davison and Asch 2011; Moore et al. 2001).
In the present investigation, the occurrence of incidence of plastics was equal to 6.8 and 5.9 for B. fibulatum and B. pterotum. Such slight differences might be due to the feeding habit of the fish, which regulate the level of plastic consumption. Such results were also obtained from lanternfishes from the Mediterranean (Romeo et al. 2016).
The present results showed that the colours of plastic fragments retrieved from the stomach of the two lanternfishes were mostly clear (white, hyaline, yellow, pink), comparable to those of many zooplankton species (Scotto Di Carlo et al. 1982; Battaglia et al. 2014; Romeo et al. 2016). On the other hand, the size of the fragments of the plastic is comparable to that of the copepods or other small zooplankton prey, therefore clarifying the affinity of swallowing these pieces.
The effects of intake of plastic particles on lanternfish have not been fully assessed but include two chief worries: physical and toxicological influences. The plastic fragments may gather in digestive tracts and be also maintained: minimum plastic pieces might be removed with the faeces of fish, while larger plastic (mesoplastics) may have a size problem in passing them via digestive tracts and lead fish to undernourishment and ultimate famishment (Boerger et al. 2010), also taking into consideration the small size of lanternfishes. The consumption of plastic performs a severe threat as they do their daily vertical migration and meet the plastic debris with density high than the water and found floating on or near the surface (Olivar et al. 2012). Sometimes, lanternfishes consume large amount of plastic with high buoyancy that prevent them to go back to deep waters, expressing a possible basis of mass death. The direct and unintended ecotoxicological effects of microplastics contact on the lanternfish biology and to the relocation of contaminants through the marine nourishment level up to top predators will continue or may be increased as the management of the plastic in the sea is enhanced.
References
Battaglia P, Andaloro F, Consoli P, Esposito V, Malara D, Musolino S, Pedà C, Romeo T (2013) Feeding habits of the Atlantic bluefin tuna, Thunnus thynnus (L. 1758), in the central Mediterranean Sea (Strait of Messina). Helgol Mar Res 67(1):97–107
Battaglia P, Esposito V, Malara D, Falautano M, Castriota L, Andaloro F (2014) Diet of the spothead lanternfish Diaphus metopoclampus (Cocco, 1829) (Pisces: Myctophidae) in the central Mediterranean Sea. Ital J Zool 81(4):530–543
Boerger CM, Lattin GL, Moore SL, Moore CJ (2010) Plastic ingestion by planktivorous fishes in the North Pacific Central Gyre. Mar Pollut Bull 60:2275–2278
Clark CW, Levy DA (1988) Diel vertical migrations by juvenile sockeye salmon and the antipredation window. Am Nat 191:271–290
Collignon A, Hecq JH, Galgani F, Collard F, Goffart A (2014) Annual variation in neustonic micro-and meso-plastic particles and zooplankton in the Bay of Calvi (Mediterranean–Corsica). Mar Pollut Bull 79(1):293–298
Davison P, Asch RG (2011) Plastic ingestion by mesopelagic fishes in the North Pacific Subtropical Gyre. Mar Ecol Progr Ser 432:173–180
Derraik JGB (2002) The pollution of the marine environment by plastic debris: a review. Mar Pollut Bull 44:842–852
DeWitte B, Devriese L, Bekaert K, Hoffman S, Vandermeersch G, Cooreman K, Robbens J (2014) Quality assessment of the blue mussel (Mytilus edulis): comparison between commercial and wild types. Mar Pollut Bull 85:146–155
Galgani F, Hanke G, Werner S, De Vrees L (2013) Marine litter within the European marine strategy framework directive. ICES J Mar Sci 70:1055–1064
Gjøsaeter J, Kawaguchi K (1980) A review of the world resources of mesopelagic fish. FAO Fish. Tech. Pap. No. 193. FIRM/TI93. 151 p
Hulley PA (1986) Myctophidae. In: Smith MM, Heemstra PC (eds) Smiths' sea fishes. Springer, Berlin, pp 282–321
Karakulak S, Salman A, Oray IK (2009) Diet composition of bluefin tuna (Thunnus thynnus L. 1758) in the Eastern Mediterranean Sea. Turk J Zool 25:757–761
Kuiter RH, Tonozuka T (2001) Pictorial guide to Indonesian reef fishes. Part 1. Eels-Snappers, Muraenidae – Lutjanidae. Zoonetics, Australia. 1–302
Lusher AL, O’Donnell C, Officer R, O'Connor I (2015) Microplastic interactions with North Atlantic mesopelagic fish. ICES J Mar Sci 73(4):1214–1225
Moore CJ, Moore SL, Leecaster MK, Weisberg SB (2001) A comparison of plastic and plankton in the North Pacific Central Gyre. Mar Pollut Bull 42:1297–1300
Moteki M, Arai M, Tsuchiya K, Okamoto H (2001) Composition of piscine prey in the diet of large pelagic fish in the eastern tropical Pacific Ocean. Fish Sci 67:1063–1074
Olivar MP, Bernal A, Moli B, Peña M, Balbin R, Castellon A, Miquel J, Massuti E (2012) Vertical distribution, diversity and assemblages of mesopelagic fishes in the western Mediterranean. Deep Sea Res I 62:53–69
Olivar MP, Moser HG, Beckley LE (1999) Lanternfish larvae from the Agulhas current (SW Indian Ocean). Sci Mar 63(2):101–120
Paxton JR, Hulley PA (1999) Myctophidae. Lanternfishes. In: Carpenter KE, Niem VH (eds) FAO species identification guide for fishery purposes. The living marine resources of the WCP. Vol. 3. Batoid fishes, chimaeras and bony fishes part 1 (Elopidae to Linophrynidae). FAO, Rome, pp 1957–1964
Riede K (2004) Global register of migratory species – from global to regional scales. Final Report of the R&D-Project 808 05 081. Federal Agency for Nature Conservation, Bonn, Germany. 329 p
Romeo T, Peda C, Fossi MC, Andaloro F, Battaglia P (2016) First record of plastic debris in the stomach of Mediterranean lanternfishes. Acta Adriat 57(1)
Scotto Di Carlo B, Costanzo G, Fresi E, Guglielmo L, Ianora A (1982) Feeding ecology and stranding mechanisms in two lanternfishes, Hygophum benoiti and Myctophum punctatum. Mar Ecol Progr Ser 9:13–24
Springer AM, Piatt JF, Shuntov VP, Van Vliet GB, Vladimirove VL, Kuzin AE, Perlov AS (1999) Marine birds and mammals of the Pacific Subarctic Gyres. Progr Oceanogr 43:443–487
Weitkamp DE, Sullivan RD (2003) Gas bubble disease in resident fish of the lower Clark Fork River. Trans Am Fish Soc 132(5):865–876
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2021 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Jawad, L.A. (2021). First Report of Plastic Fragments in the Lanternfishes Collected from the Sea of Oman. In: Jawad, L.A. (eds) The Arabian Seas: Biodiversity, Environmental Challenges and Conservation Measures. Springer, Cham. https://doi.org/10.1007/978-3-030-51506-5_60
Download citation
DOI: https://doi.org/10.1007/978-3-030-51506-5_60
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-51505-8
Online ISBN: 978-3-030-51506-5
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)