Microplastics in gentoo penguins from the Antarctic region



There is growing evidence that microplastic pollution (<5 mm in size) is now present in virtually all marine ecosystems, even in remote areas, such as the Arctic and the Antarctic. Microplastics have been found in water and sediments of the Antarctic but little is known of their ingestion by higher predators and mechanisms of their entry into Antarctic marine food webs. The goal of this study was to assess the occurrence of microplastics in a top predator, the gentoo penguin Pygoscelis papua from the Antarctic region (Bird Island, South Georgia and Signy Island, South Orkney Islands) and hence assess the potential for microplastic transfer through Antarctic marine food webs. To achieve this, the presence of microplastics in scats (as a proof of ingestion) was investigated to assess the viability of a non-invasive approach for microplastic analyses in Antarctic penguins. A total of 80 penguin scats were collected and any microplastics they contained were extracted. A total of 20% of penguin scats from both islands contained microplastics, consisting mainly of fibers and fragments with different sizes and polymer composition (mean abundance of microplastics: 0.23 ± 0.53 items individual−1 scat, comprising seven different polymers), which were lower values than those found for seabirds in other regions worldwide. No significant differences in microplastic numbers in penguin scats between the two regions were detected. These data highlight the need for further assessment of the levels of microplastics in this sensitive region of the planet, specifically studies on temporal trends and potential effects on penguins and other organisms in the Antarctic marine food web.


Plastic pollution (whether at the macro or the micro scale) is one of today’s environmental issues of highest concern among scientists, policy makers and the general public1,2,3,4. One aspect of plastic pollution that has received increasing attention in recent years is that of microplastics, defined as any plastic particles smaller than 5 mm, which are either manufactured as small particles or originated from the fragmentation of larger plastic items5,6. These particles may be subjected to a range of complex processes in the environment (weathering, embrittlement, aggregation), producing a variety of particles with different characteristics (shape, size and density)2,7. Additionally, they can leach out chemical additives and adsorb organic chemicals that are found in the environment, and some such compounds can bioaccumulate, posing a potential detriment to species and ecosystems4,8.

Microplastics are present in most habitats including rivers, lakes, oceans, soil and air9,10,11 and are bioavailable to ingestion by a variety of aquatic biota (from zooplankton to megafauna)12,13,14,15,16. Despite their widespread occurrence, their effects on wild organisms have yet to be quantified4,8. These particles have been detected in remote areas such as the Arctic and the Antarctic regions17,18. These polar ecosystems have recently received heightened attention regarding microplastic pollution, and there are several studies that have reported evidence of these particles in Arctic surface waters19,20, in high concentrations in the sea ice across the Arctic Ocean18 and in benthic organisms21.

Less is known about the occurrence of microplastic in the Southern Ocean17, where they have only been detected in seawater22,23 and sediments24,25. However, it has been shown that Antarctic krill Euphausia superba can ingest microplastics in laboratory experiments26, but less is known regarding the levels of microplastics in wild Antarctic marine organisms (but see the reports on ingestion of plastic debris of larger sizes by petrels breeding in Antarctica27 and fur seals28.

Despite its remoteness, the Antarctic environment may be subject to local plastic pollution sources from fishing activities, tourism or research stations17. Microplastics could therefore reach Antarctica via three distinct routes: from local human activities, from outside Antarctica in atmosphere/ocean circulation or bio-transport by organisms that migrate to Antarctica from waters further north and induced by storm-driven dispersal and global warming29. However, the data available regarding these processes in the Antarctic are still so limited that the Scientific Committee on Antarctic Research has recently created an action group on plastic pollution (https://www.scar.org/science/plastic/about/).

Within Antarctic marine organisms, seabirds are considered as one of the most convenient bioindicators of environmental change and have been also proposed as indicators for plastic pollution in many marine environments30,31. Antarctic penguins, such as gentoo penguins Pygoscelis papua, have been considered a standard organism for monitoring contamination in Antarctic marine ecosystems32,33. Gentoo penguins are also an appropriate species in this context due to their limited movements outside their home range throughout the year, as shown by tracking data, diet and genetic studies34,35,36,37,38, which exclude the possibility of ingesting plastic debris from waters outside Antarctica. The aim of this study was thus to assess the occurrence of microplastics in an Antarctic marine predator in the wild, the gentoo penguin, (using their scats as proxy of ingestion), to identify and characterize the microplastics found, and discuss their likely source.


A total of 80 scats were collected (50 scats at Bird Island and 30 scats at Signy Island, Fig. 1). All isolated particles (suspected microplastics) were characterised, but only those confirmed by micro-Fourier Transform Infrared Spectroscopy (µ-FTIR) as synthetic/semi-synthetic were considered in the total counts. In addition, we identified two particles of cellulose and five other particles as natural compounds; these were excluded from the analyses. No microplastics were detected in any of the blank replicates.

Figure 1

Map of location of the sampling islands (Bird Island and Signy Island) in the Scotia Sea.

No significant differences between the two islands were found regarding the number of scats having microplastics (PERMANOVA test: pseudo-F = 0.0501 and p (MC) = 0.8283) and 20% of scats were found with microplastics in Bird Island (13 microplastics in 10/50 scats) and 20% of scats with microplastics were recorded in Signy Island (6 microplastics in 6/30 scats).

In total, 19 microplastics were identified from the scats (0.23 ± 0.53 items.scat−1) and microfibers were the most abundant shape in the scats from both islands (58%), followed by fragments (26%) and films (16%) of different colours and sizes (Table 1 and Fig. 2). Of the 16 samples with microplastics, there was on average 1.19 ± 0.54 items.scat−1: range 1–3 particles) with different mean values from both islands (Bird Island: 1.3 ± 0.67 items.scat−1 and Signy Island: 1 items.scat−1). Microplastics measured on average 1266 ± 1378 µm with a minimum length of 76 µm and a maximum of 4945 µm (Table 1). Mean fiber length was 1889 ± 1448 µm (range 408–4945 µm), while fragments and films measured on average 312 ± 229 µm (range 76–738 µm).

Table 1 Identification of the synthetic particles found in penguin scats collected at the Southern Ocean. For the infrared characteristic band of the microplastic samples please see supplementary material.
Figure 2

Example of microplastics isolated from penguin scats and analysed using u-FTIR. (A) Blue polyester fragment; (B) Transparent polyethylene film; (C) Transparent polyacrylonitrile fiber (D) Mixed polyester fibers; (E) Blue polyacrylate fragment and (F) Transparent Rayon film. Scale Bars = 1 mm. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article).

Seven different polymer types were identified in penguin scats from both locations (Table 1). Polyester accounted for the largest proportion (60%) being mainly microfibers, followed by fibers of the semi-synthetic cellulose polymer Rayon (15%, only detected in Signy Island), whereas the other particles (fragments and films) were identified as single polymers (polyacrylonitrile, polypropylene, polyethylene and polyacrylate, Table 1 and Supplementary material). One particle was classified as “unidentified synthetic” despite the clear similarity with a synthetic poly(ethylacrylate:st:acrylamide), however, additional bands are observed that may be due to degradation of the polymer or to the presence of another compound (see Fig. 1S–G and Table 1S). Nevertheless, due to its anthropogenic origin this was considered in the total counts of microplastics. In addition, the composition of the polymers varied in the two islands with 3 polymer types being recorded in Signy Island (Rayon, polyacrylate and polyester), while a higher diversity was recorded for microplastics found in Bird Island (polyacrylamide, polyacrylonitrile, polyester, polypropylene and polyethylene, Table 1).


To our knowledge, this is the first study to show that microplastics are present in the gastrointestinal tract of penguins feeding in Antarctic waters and therefore potentially widespread in the Antarctic marine food web. Microplastics have probably been ingested and taken up by gentoo penguins either through direct ingestion (e.g. due to misidentification of microplastics for food), indirect ingestion via contaminated prey (e.g. Antarctic krill is capable of ingesting microplastics in laboratory experiments26, so it is likely that it may also ingest microplastics in the wild), and/or incidental ingestion via contaminated water/sediments (i.e. microplastics in Antarctic sediments have been noted23,24,25 or while preening their feathers). According to several studies, the diet of gentoo penguins usually includes a high percentage of Antarctic krill37,38,39,40, so the observed contamination of gentoo scats implies that other Antarctic krill dependent species may also be susceptible of being contaminated with microplastics and need to be addressed in future research. Antarctic krill play a key role in Antarctic marine ecosystems41, in which the majority of primary productivity is passed to secondary consumers through a single main grazing species (i.e. Antarctic krill)42. Thus, microplastics may be passed among numerous organisms within the Antarctic marine food web.

In this study, 80 scats from gentoo penguins were analysed from two islands from the Southern Ocean (Bird Island and Signy Island), with no significant differences in the amount of contaminated scats between sites. However, there were dissimilarities in the polymeric composition of the particles. These differences in polymer composition of the extracted particles can be attributed to potential different point sources of plastic pollution in these regions. Both islands do have research stations and fisheries operating in their waters43,44, but Bird Island is located considerably closer to the Antarctic Polar Front and potentially more influenced by pollution coming from the Antarctic Circumpolar Current and from the north, whereas Signy Island is located much closer to the Antarctic continent, further away from potential northern sources of pollution less influenced by Antarctic Circumpolar current45,46. However, to categorically attribute cause, or source, would require background data on the prevalence of different compound types with latitude in order to make any deductions with confidence.

At both our study sites, microfibers were the main category of microplastics recorded, which agrees with a general pattern reported in the marine environment17,19 and in similar studies performed during ingestion studies for marine species from other habitats12,14,16. The potential sources of these microfibers in other marine environments has been attributed to the generation of fibers during clothes washing9, or also from the fragmentation of nets and ropes from fisheries discarded in the oceans10. Microplastic fragments of different shapes and colours will be difficult to trace to source based simply on polymer composition. Moreover, currently available information on the distribution of microplastics is not sufficient to identify potential sources of microplastic pollution and hence now warrants further assessment47,48. In the southwest Atlantic, additional point sources from anthropogenic activities can be diverse including direct sources via disposal, inadequate management of waste produced by ships or from touristic activitites17. Narrowing down the source of microplastic will only become feasible with background data on prevalence of different compound types.

Existing data on the concentration of a range of other persistent contaminants in air, snow and marine organisms in the Antarctic environment has already demonstrated that these pollutants are transported from other continents in the Southern Ocean49, and this could be also the case with plastic debris. For this reason, it is also important to point out the potential contribution of the atmospheric fallout48,50 as input of microplastics, especially microfibers in this area.

The proportion of scats containing microplastic was relatively low, when compared with results for other seabirds, or other top predators, from other environments31,51, which is consistent with the limited number of studies that reported similar relatively low values of these anthropogenic particles in water and sediments in this region17.

Overall, our data confirm that microplastics are present in penguins from the Antarctic and sub-Antarctic region. We have shown that penguin scat analysis is a suitable approach for assessing anthropogenic changes in Antarctica regarding the presence and distribution of microplastics since it is a non-invasive method and it can be considered a suitable first approach for areas or species that are understudied. However, there are also limitations, since microplastics recovered from scat samples represent those particles that were ingested and excreted and caution is recommended when assessing potential effects of those plastics passing through the digestive systems of these species31. Further work is needed to evaluate the fate and transport of microplastics in the Antarctic ecosystem and their impacts on key species. Indeed, Antarctica may still be relatively isolated from microplastic pollution, but not completely so; this data refers to 2009 and since it is known that plastic pollution has increased and is expected to increase in the near future52, the situation can change rapidly. Surface currents connect Antarctica with the rest of the planet and may allow the entrance of microplastics17,29,53. In contrast, local sources of microplastics are relatively small as the number of research stations, tourist vessels and fishing vessels is still small, making Antarctica very sparsely populated compared with elsewhere on the planet. Nevertheless, some authors17 estimate that about 25.5 billion fibers of synthetic origin are potentially entering the Southern Ocean per decade from clothes laundering, making a substantial contribution to the local levels of microplastics. A much wider investigation would be needed to reveal the full spectrum of microplastic pollution in Antarctica.


Gentoo penguin scats were collected from colonies at Bird Island, South Georgia (54°S, 38°W) and Signy Island, South Orkney Islands (60°S, 45°W), during the austral summer of 2009 (Fig. 1). Samples were collected by hand using nitrile gloves and placed into sterile collection plastic bags. Scats were randomly collected across sites to avoid the possibility of collecting scats from the same individual. Scats were collected from the ground immediately after defecation following the procedures described in37. Each scat was frozen (−20 °C) for further analyses in the laboratory. Each scat was then defrosted and transferred to a clean glass beaker (250 ml) and 100 ml of potassium hydroxide solution (KOH, 10%) was added to digest the organic material. After 24 h of digestion at 40 °C, the floating phase was vacuum filtered through a 1.2 µm glass microfibre filter. The residue was transferred to a new glass beaker and hydrogen peroxide (H2O2, 10%, 24 h) was added to increase the recovery of potential particles trapped in the residue and the filtration was repeated. Each filter was placed in a Petri dish and placed to dry in an oven at 40 °C. Three identical blanks in total with milliQ water were set up, using the same procedures to account for background contamination. The filter papers were then examined under a stereomicroscope LEICA M80 (Microsystems GmbH, Wetzlar, Germany), to identify potential microplastics. Particles exhibiting the appearance of microplastics/anthropogenic particles were kept on filters, photographed using the image analysis system IC80 HD Camera with Leica Application Suite (LAS) software and placed between two microscopic slides, until further analysis. The particles were categorized according to their shape and colour and their largest cross-section (size) was measured. The lower limit of resolution and detection of microplastics was 60 µm. The chemical composition of all particles collected was determined by micro-Fourier Transform Infrared Spectroscopy (µ-FTIR) and infrared spectra were acquired in a Nicolet® Nexus spectrophotometer coupled to a Continuum microscope (15× objective) with a MCT-A detector cooled by liquid nitrogen, following the technical procedures described in14. The polymer identification was based on spectral absorption bands and confirmed by comparison with a spectral library database. To avoid potential airborne contamination, all liquids used were previously filtered through a 1.2 µm glass microfibre filter and glass containers rinsed with ultrapure water before reuse. Moreover, the entire process of analyses of microplastics (extraction and identification) was conducted by only one person in a closed and restricted access laboratory. Laboratory work was carried out using a cotton lab coat and nitrile gloves.

Microplastic concentrations were compared between sites using a permutational multivariate analysis of variance (PERMANOVA54), as data were not normally distributed (Kolmogorov-Smirnov: p < 0.05) and not homoscedastic (Levene’s test p < 0.05). All statistical analyses were performed using PRIMER v.6 and its add-on package PERMANOVA+54.


  1. 1.

    Marine Plastic Debris and Microplastics: Global lessons and research to inspire action and guide policy change. United Nations Environment Programme, Nairobi (2016).

  2. 2.

    GESAMP (2016). “Sources, fate and effects of microplastics in the marine environment: part two of a global assessment” (Kershaw, P. J., and Rochman, C. M., eds). (IMO/FAO/UNESCO-IOC/UNIDO/WMO/IAEA/UN/UNEP/UNDP Joint Group of Experts on the Scientific Aspects of Marine Environmental Protection). Rep.Stud. GESAMP No. 93, 220 p. (2016).

  3. 3.

    Andrady, A. L. The plastic in microplastics: A review. Mar. Pollut. Bull. 119, 12–22 (2017).

    CAS  Article  Google Scholar 

  4. 4.

    Burns, E. E. & Boxall, A. B. A. Microplastics in the aquatic environment: Evidence for or against adverse impacts and major knowledge gaps. Environ. Toxicol. Chem. 37(11), 2776–2796 (2018).

    CAS  Article  Google Scholar 

  5. 5.

    Thompson, R. C. et al. Lost at sea: where is all the plastic? Science 304, 838 (2004).

    CAS  Article  Google Scholar 

  6. 6.

    Arthur, C., Baker, J. & Bamford, H. (Eds). Proceedings of the International Research Workshop on the Occurrence, Effects and Fate of Microplastic Marine Debris. September 9–11, 2008. NOAA Technical Memorandum NOS-OR&R-30 (2009).

  7. 7.

    Hermabessiere, L. et al. Occurrence and effects of plastic additives on marine environments and organisms: A review. Chemosphere 182, 781–793 (2017).

    ADS  CAS  Article  Google Scholar 

  8. 8.

    SAPEA, Science Advice for Policy by European Academies. A Scientific Perspective on Microplastics in Nature and Society. Berlin: SAPEA. (2019).

  9. 9.

    Andrady, A. L. Microplastics in the marine environment. Mar. Pollut. Bull. 62, 1596–1605 (2011).

    CAS  Article  Google Scholar 

  10. 10.

    Browne, M. A. et al. Accumulation of microplastic on shorelines worldwide: sources and sinks. Environ. Sci. Technol. 45(21), 9175–9179 (2011).

    ADS  CAS  Article  Google Scholar 

  11. 11.

    Wagner, M., & Lambert, S. Freshwater Microplastics: Emerging Environmental Contaminants? Cham, Switzerland: Springer International Publishing AG (2018).

  12. 12.

    Cole, M. et al. Microplastic ingestion by zooplankton. Environ. Sci. Technol. 47, 6646–6655 (2013).

    ADS  CAS  Article  Google Scholar 

  13. 13.

    Besseling, E. et al. Microplastic in a macro filter feeder: Humpback whale Megaptera novaeangliae. Mar. Pollut. Bull. 95, 248–252 (2015).

    CAS  Article  Google Scholar 

  14. 14.

    Bessa, F. et al. Occurrence of microplastics in commercial fish from a natural estuarine environment. Mar. Pollut. Bull. 128, 575–584 (2018).

    CAS  Article  Google Scholar 

  15. 15.

    Donohue, M. J. et al. Evaluating exposure of northern fur seals, Callorhinus ursinus, to microplastic pollution through fecal analysis. Mar. Pollut. Bull 138, 213–221 (2019).

    CAS  Article  Google Scholar 

  16. 16.

    Nelms, S. E. et al. Microplastics in marine mammals stranded around the British coast: ubiquitous but transitory? Sci. Rep. 9, 1075 (2019).

    ADS  CAS  Article  Google Scholar 

  17. 17.

    Waller, C. L. et al. Microplastics in the Antarctic marine system: An emerging area of research. Sci. Total Environ. 598, 220–227 (2017).

    ADS  CAS  Article  Google Scholar 

  18. 18.

    Peeken, I. et al. Arctic sea ice is an important temporal sink and means of transport for microplastic. Nat. Commun. 9(1), 1505 (2018).

    ADS  Article  Google Scholar 

  19. 19.

    Lusher, A. L., Tirelli, V., O’Connor, I. & Officer, R. Microplastics in Arctic polar waters: the first reported values of particles in surface and sub-surface samples. Sci. Rep. 5, 14947 (2015).

    ADS  CAS  Article  Google Scholar 

  20. 20.

    Kanhai, L. D. K. et al. Microplastics in sub-surface waters of the Arctic Central Basin. Mar. Pollut. Bull. 130, 8–18 (2018).

    CAS  Article  Google Scholar 

  21. 21.

    Fang, C. et al. Microplastic contamination in benthic organisms from the Arctic and sub-Arctic regions. Chemosphere 209, 298–306 (2018).

    ADS  CAS  Article  Google Scholar 

  22. 22.

    Isobe, A., Uchiyama-Matsumoto, K., Uchida, K. & Tokai, T. Microplastics in the Southern Ocean. Mar. Pollut. Bull. 114, 623–626 (2017).

    CAS  Article  Google Scholar 

  23. 23.

    Cincinelli, A. et al. Microplastic in the surface waters of the Ross Sea (Antarctica): occurrence, distribution and characterization by FTIR. Chemosphere 175, 391–400 (2017).

    ADS  CAS  Article  Google Scholar 

  24. 24.

    Munari, C. et al. Microplastics in the sediments of Terra Nova Bay (Ross Sea, Antarctica). Mar. Pollut. Bull. 122(1-2), 161–165 (2017).

    CAS  Article  Google Scholar 

  25. 25.

    Reed, S., Clark, M., Thompson, R. & Hughes, K. A. Microplastics in marine sediments near Rothera Research Station, Antarctica. Mar. Pollut. Bull. 133, 460–463 (2018).

    CAS  Article  Google Scholar 

  26. 26.

    Dawson, A. L. et al. Turning microplastics into nanoplastics through digestive fragmentation by Antarctic krill. Nat. Commun. 9, 1001 (2018).

    ADS  Article  Google Scholar 

  27. 27.

    Van Franeker, J. A. & Bell, P. J. Plastic ingestion by petrels breeding in Antarctica. Mar. Pollut. Bull. 19, 672–674 (1988).

    Article  Google Scholar 

  28. 28.

    Eriksson, C. & Burton, H. Origins and Biological Accumulation of Small Plastic Particles in Fur-seal Scats from Macquarie Island. Ambio 32, 380–384 (2003).

    Article  Google Scholar 

  29. 29.

    Fraser, C. I. et al. Antarctica’s ecological isolation will be broken by storm-driven dispersal and warming. Nat. Clim. Change 8, 704–708 (2018).

    ADS  Article  Google Scholar 

  30. 30.

    Boersma, P. D. Penguins as marine sentinels. Bioscience 58, 597–607 (2008).

    Article  Google Scholar 

  31. 31.

    Provencher, J. F. et al. Garbage in guano? Microplastic debris found in faecal precursors of seabirds known to ingest plastics. Sci. Total Environ. 644, 1477–1484 (2018).

    ADS  CAS  Article  Google Scholar 

  32. 32.

    Ellis, D. S., Cipro, C. V. Z., Ogletree, C. A., Smith, K. E. & Aronson, R. B. A 50-year retrospective of persistent organic pollutants in the fat and eggs of penguins of the Southern Ocean. Environ. Pollut. 241, 155–163 (2018).

    CAS  Article  Google Scholar 

  33. 33.

    Trathan, P. N. et al. Pollution, habitat loss, fishing and climate change as critical threats to penguins. Conserv. Biol. 29, 31–41 (2015).

    Article  Google Scholar 

  34. 34.

    Tanton, J. L., Reid, K., Croxall, J. P. & Trathan, P. N. Winter distribution and behaviour of gentoo penguins Pygoscelis papua at South Georgia. Polar Biol. 27, 299–303 (2004).

    Article  Google Scholar 

  35. 35.

    Clucas, G. V. et al. Dispersal in the sub-Antarctic: king penguins show remarkably little population genetic differentiation across their range. BMC Evol. Biol. 16, 211 (2016).

    Article  Google Scholar 

  36. 36.

    Hinke, J. T. et al. Identifying Risk: Concurrent Overlap of the Antarctic Krill Fishery with Krill-Dependent Predators in the Scotia Sea. PLoS One 12(1), e0170132 (2017).

    Article  Google Scholar 

  37. 37.

    Xavier, J. C. et al. Sexual and individual foraging segregation in Gentoo penguins Pygoscelis papua from the Southern Ocean during an abnormal winter. PloS One 12, e0174850 (2017).

    Article  Google Scholar 

  38. 38.

    Waluda, C. M., Hill, S. L., Peat, H. J. & Trathan, P. N. Long-term variability in the diet and reproductive performance of penguins at Bird Island, South Georgia. Mar. Biol. 164, 39 (2017).

    Article  Google Scholar 

  39. 39.

    Ratcliffe, N. & Trathan, P. N. A review of the diet and at sea-distribution of penguins breeding within the CCAMLR convention area. CCAMLR Sci. 18, 75–114 (2011).

    Google Scholar 

  40. 40.

    Xavier, J. et al. Seasonal prey switching in non-breeding gentoo penguins related to a wintertime environmental anomaly around South Georgia. Polar Biol. 41, 2323–2335 (2018).

    Article  Google Scholar 

  41. 41.

    Everson, I. Krill: biology, ecology and fisheries. Blackwell Science Ltd, Oxford (2000).

  42. 42.

    Atkinson, A. et al. Sardine cycles, krill declines, and locust plagues: revisiting ‘wasp-waist’ food webs. Trends Ecol. Evol. 29, 309–316 (2014).

    Article  Google Scholar 

  43. 43.

    Kock, K-H. Antarctic fish and fisheries. Cambridge University Press, Cambridge. (1992).

  44. 44.

    Everson, I. Southern Ocean fisheries. In: Steele J, Turekian K, Thorpe SA (eds) Encyclopedia of ocean sciences. Academic Press, San Diego, CA. (2001).

    Google Scholar 

  45. 45.

    Orsi, A. H., Whitworth, T. III. & Nowlin, W. D. J. On the meridional extent and fronts of the Antarctic Circumpolar. Current. Deep-Sea Res. 42, 641–673 (1995).

    Article  Google Scholar 

  46. 46.

    Rintoul, S. R. The global influence of localized dynamics in the Southern Ocean. Nature 558, 209–218 (2018).

    ADS  CAS  Article  Google Scholar 

  47. 47.

    Lacerda, A. L. D. F. et al. Plastics in sea surface waters around the Antarctic Peninsula. Sci. Rep. 9(1), 3977 (2019).

    ADS  Article  Google Scholar 

  48. 48.

    Absher, T. M. et al. Incidence and identification of microfibers in ocean waters in Admiralty Bay Antarctica. Environ. Sci. Pollut. R. 26(1), 292–298 (2019).

    CAS  Article  Google Scholar 

  49. 49.

    Bargagli, R. Environmental contamination in Antarctic ecosystems. Sci. Total Environ. 400, 212–226 (2008).

    ADS  CAS  Article  Google Scholar 

  50. 50.

    Dris, R., Gasperi, J., Saad, M., Mirande, C. & Tassin, B. Synthetic fibers in atmospheric fallout: a source of microplastics in the environment? Mar. Pollut. Bull. 104, 290–293 (2016).

    CAS  Article  Google Scholar 

  51. 51.

    Terepocki, A. K., Brush, A. T., Kleine, L. U., Shugart, G. W. & Hodum, P. Size and dynamics of microplastic in gastrointestinal tracts of northern fulmars (Fulmarus glacialis) and sooty shearwaters (Ardenna grisea). Mar. Pollut. Bull. 116, 143–150 (2017).

    CAS  Article  Google Scholar 

  52. 52.

    Jambeck, J. R. et al. Plastic waste inputs from land into the ocean. Science 347, 768e771 (2015).

    Article  Google Scholar 

  53. 53.

    Fraser, C. I., Kay, G. M., Plessis, M. & Ryan, P. G. Breaking down the barrier: dispersal across the Antarctic Polar Front. Ecography 40, 235–237 (2017).

    Article  Google Scholar 

  54. 54.

    Anderson, M. J., Gorley, R. N. & Clarke, K. R. PERMANOVA+ for PRIMER: Guide to Software and Statistical Methods. PRIMER-E Ltd., Plymouth, UK (2008).

Download references


FB acknowledges the financial support received from Fundação para a Ciência e Tecnologia (FCT, Portugal) through the strategic project UID/MAR/04292/2019, granted to MARE and through a post-doc scholarship grant (SFRH/BPD/99747/2014) and the contract with the University of Coimbra (IT057-18-7252). This work is part of the monitoring long-term project BAS-CEPH and SCAR Ant-ERA, SCAR EGBAMM and ICED research programs. The authors also acknowledge Derren Fox for the collection of samples in Signy Island and Laura Gerrish of the BAS Mapping And Geographic Information Centre (MAGIC) for producing Figure 1.

Author information




F.B. and J.C.X. conceived the idea of this study. F.B. and V.O. performed laboratory analyses. J.C.X., N.R., P.S., J.C.M., C.M.W. and P.N.T. discussed the results. F.B. analysed the data and prepared the manuscript and all authors contributed substantially to revisions.

Corresponding author

Correspondence to Filipa Bessa.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Bessa, F., Ratcliffe, N., Otero, V. et al. Microplastics in gentoo penguins from the Antarctic region. Sci Rep 9, 14191 (2019). https://doi.org/10.1038/s41598-019-50621-2

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing