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Abundance and composition of near surface microplastics and plastic debris in the Stockholm Archipelago, Baltic Sea
Stockholm University, Faculty of Science, Department of Environmental Science and Analytical Chemistry.
Stockholm University, Faculty of Science, Department of Environmental Science and Analytical Chemistry. Aquabiota Water Research, Sweden.ORCID iD: 0000-0002-7082-0990
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.ORCID iD: 0000-0001-5784-7673
Stockholm University, Faculty of Science, Department of Environmental Science and Analytical Chemistry.ORCID iD: 0000-0003-2562-7339
Number of Authors: 42017 (English)In: Marine Pollution Bulletin, ISSN 0025-326X, E-ISSN 1879-3363, Vol. 120, no 1-2, p. 292-302Article in journal (Refereed) Published
Abstract [en]

We collected plastic debris in the Stockholm Archipelago using a manta trawl, and additionally along a transect in the Baltic Sea from the island of Gotland to Stockholm in a citizen science study. The samples were concentrated by filtration and organic material was digested using hydrogen peroxide. Suspected plastic material was isolated by visual sorting and 59 of these were selected to be characterized with Fourier transform infrared spectroscopy. Polypropylene and polyethylene were the most abundant plastics identified among the samples (53% and 24% respectively). We found nearly ten times higher abundance of plastics near central Stockholm than in offshore areas (4.2 x 10(5) plastics km(-2) compared to 4.7 x 10(4) plastics km(-2)). The abundance of plastic debris near Stockholm was similar to urban areas in California, USA, and the overall abundance in the Stockholm Archipelago was similar to plastic abundance reported in the northwestern Mediterranean Sea.

Place, publisher, year, edition, pages
2017. Vol. 120, no 1-2, p. 292-302
Keywords [en]
Microplastic, Plastic pollution, Sea surface, Baltic Sea, Manta trawl, FTIR
National Category
Earth and Related Environmental Sciences Biological Sciences
Research subject
Applied Environmental Science
Identifiers
URN: urn:nbn:se:su:diva-147169DOI: 10.1016/j.marpolbul.2017.04.062ISI: 000407539300044PubMedID: 28527744OAI: oai:DiVA.org:su-147169DiVA, id: diva2:1143735
Available from: 2017-09-22 Created: 2017-09-22 Last updated: 2025-01-31Bibliographically approved
In thesis
1. Chemical Pollutants Released to the Marine Environment by Degradation of Plastic Debris
Open this publication in new window or tab >>Chemical Pollutants Released to the Marine Environment by Degradation of Plastic Debris
2018 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Since the beginning of the mass production in the 1940s, plastic has been manufactured in quickly increasing amounts. Plastic debris accumulates in the environment and lately much attention has been drawn to the pollution in the world’s oceans. Despite the rapid development and ubiquitous presence of plastic, degradation in the marine environment and potential risks associated with plastic are not fully understood. Thus, these knowledge gaps were addressed in this thesis, which adds information about exposure and hazards of marine plastic debris.

Although sampling studies have been conducted all over the world, the concentrations of plastic debris in the Baltic Sea have hardly been investigated. In Paper I, the level and distribution of plastic debris in the Stockholm Archipelago were assessed. Plastic concentrations were higher close to suspected point sources compared to remote areas. Fibers accounted for the most common form and the predominant polymer types were polypropylene (PP) and polyethylene (PE).

In Paper II, the literature was critically reviewed for the most important degradation pathways for plastic under environmentally relevant conditions. Ultraviolet (UV) radiation, leading to photo-oxidation, is the most important initiating factor for buoyant plastic. Consequently, a UV lamp was used in Paper III for an artificial weathering setup in the laboratory to degrade pristine plastics and analyze the chemical leachates by liquid chromatography-mass spectrometry (LC-MS) for degradation products using a nontarget approach. Carboxylic acids and dicarboxylic acids of polymer fragments were the most commonly identified degradation products of the plastic polymers, confirming predictions made in Paper II.

To evaluate potential hazards posed by leachates from weathering plastic debris to marine organisms, an acute toxicity screening study with Nitocra spinipes was conducted in Paper IV. Field-exposed plastic and the corresponding newly purchased plastic were artificially aged with the same weathering setup as in Paper III. Poly(vinyl chloride) (PVC) and PP leachates were generally most toxic, while leachates from polystyrene (PS) and poly(ethylene terephthalate) (PET) were least toxic among the tested materials. For plastics, which were supposed to contain only few additives, we observed no difference in toxicity between leachates from the field-exposed and the newly purchased plastic. However, the other plastic products exposed to the marine environment were more toxic than their corresponding newly bought products. This indicates that the toxicity of the leachates not only depends on the polymer type, but also on the weathering condition of the plastic.

Place, publisher, year, edition, pages
Stockholm: Department of Environmental Science and Analytical Chemistry, Stockholm University, 2018. p. 36
Keywords
Plastic, microplastic, degradation, leachates, weathering, photo-oxidation, marine environment, toxicity
National Category
Environmental Sciences
Research subject
Applied Environmental Science
Identifiers
urn:nbn:se:su:diva-155581 (URN)978-91-7797-167-2 (ISBN)978-91-7797-168-9 (ISBN)
Public defence
2018-06-12, Nordenskiöldsalen, Geovetenskapens hus, Svante Arrhenius väg 12, Stockholm, 10:00 (English)
Opponent
Supervisors
Note

At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 4: Manuscript.

Available from: 2018-05-18 Created: 2018-04-25 Last updated: 2022-02-26Bibliographically approved

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Gewert, BeritOgonowski, MartinBarth, AndreasMacLeod, Matthew

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