Literature DB >> 31867422

Data on microplastic contamination of the Baltic Sea bottom sediment samples in 2015-2016.

Elena Esiukova1, Mikhail Zobkov2, Irina Chubarenko1.   

Abstract

The contamination by microplastics particles (MPs, 0.2-5 mm) in bottom sediments of the Baltic Sea is quantified. In total, 53 sediment samples were obtained in 8 cruises of research vessels in July-October 2015 and March-December 2016. The depths from 3 to 215 m in the Gotland, Gdansk, and Bornholm Basins are covered. Primary data is provided, along with exhaustive information on sampling dates and coordinates, depths, sampling methods, extracting procedures, control measures, detection techniques, and verification by μ-Raman spectroscopy. Number of pieces per kg dry weight is determined separately for fibres, films, and fragments. Distributions by size, plastic colour, and plastic type are presented. Modified NOAA method and μ-Raman spectroscopy were applied to obtain the data, thus they can be used for comparative analyses.
© 2019 The Authors.

Entities:  

Keywords:  Bottom; Contamination; Microplastics; Modified NOAA method; Sediments; μ-Raman spectroscopy

Year:  2019        PMID: 31867422      PMCID: PMC6906683          DOI: 10.1016/j.dib.2019.104887

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table Microplastic contamination in bottom sediments of the Baltic Sea Proper in 2015–2016 is documented. A benchmark for future studies dedicated to microplastic contamination in the Baltic Sea is presented. Obtained data can be used for comparative analysis of plastic contamination in bottom sediments of other seas and oceans. Number of pieces per kg dry weight, spatial distribution, types of particles (fibres, films, fragments), as well as size, colour, and plastic types are reported.

Data

The dataset contains information on microplastics (MPs, 0.2–5 mm) content in 53 bottom sediment samples collected in 8 cruises of research vessels in the Gotland, Gdansk and Bornholm basins of the Baltic Sea in July–October 2015 and March–December 2016. Sampling sites (Fig. 1), their geographic coordinates, sample masses, and sediment types (Table 1) are presented. MPs content is provided in total number of pieces (fibres, films, and fragments) in a sample, and in pieces per kg dry weight (pcs per kg DW) (Table 2). Laboratory analysis workflow is described (Fig. 2). Photos of nine selected MPs specimens extracted from sediments are presented (Fig. 3). Polymer types were identified by the μ-Raman spectroscopy (Table 3). The Raman spectra of typical MPs are characterized by the hit ratio to a certain polymer type (Fig. 4).
Fig. 1

Study area and sampling stations*.

* The maps were prepared with ArcGis 10.2.2 software, Natural Earth and HELCOM MADS spatial data. Depth contours from Ref. [4].

Table 1

Expedition data, sampling sites locations and sediment characteristics.

№ sampling stationsVessel-stationDateLatitudeLongitudeDepth, mSamplerSampling square, m2Mass of sample WW, kgSediment type
1boat-9July 3, 201554.5001919.686399hand-operated drag6.7Mixed medium to coarse sand
2boat-3October 9, 201554.6298319.868673hand-operated drag14.5Mixed medium or coarse sand
3boat-5October 9, 201554.6301719.866535hand-operated drag11.8Fine sand
4boat-10October 9, 201554.6390519.84110hand-operated drag12.5Mixed medium or coarse sand
5boat-15October 9, 201554.6355719.83215hand-operated drag8.1Fine sand
6boat-20October 9, 201554.6427519.7863720hand-operated drag10.1Sand, gravel, stones
7boat-25October 9, 201554.6500719.757225hand-operated drag6.5Fine sand
8boat-30October 9, 201554.6722519.687730hand-operated drag10.4Mixed medium or coarse sand
9NORD-1March 30, 201655.0407720.437932.6Van Veen Grab0.414.4Fine sand
10NORD-2March 30, 201654.9882520.3323525Van Veen Grab0.411.3Fine sand
11NORD-3March 30, 201654.9709820.3190718Van Veen Grab0.219.3Mixed medium or coarse sand
12NORD-4March 30, 201654.9578820.3004311.5Van Veen Grab0.718.3Fine sand
13Sht 131-001March 31, 201654.8647619.34937109“Ocean-50” Grab0.3758.4Mud
14Sht 131-002March 31, 201655.1006719.22613101“Ocean-50” Grab0.18756.7Clayey mud
15Sht 131-003March 31, 201655.3385819.0997481“Ocean-50” Grab0.211.5Clayey mud
16Sht 131-004March 31, 201655.5953319.0287787.5“Ocean-50” Grab0.1253.5Mud
17Sht 131-006April 1, 201655.3314820.5618731“Ocean-50” Grab0.2516.9Fine sand
18Sht 131-007April 1, 201655.3004320.1742847“Ocean-50” Grab0.251.6Sand, gravel, stones
19Sht 131-008April 1, 201655.1673819.8326368“Ocean-50” Grab0.12.2Mud
20Sht 131-010April 2, 201655.583419.033881Van Veen Grab0.110.5Fine silty mud
21Sht 131-011April 2, 201655.8750218.93692106“Ocean-50” Grab0.2511.1Mud
22Sht 131-013April 5, 201655.9107519.05808109“Ocean-50” Grab0.1252.2Mud
23Sht 131-014April 5, 201655.8934719.06263109“Ocean-50” Grab0.1251.3Mud
24Sht 131-015April 5, 201655.8810219.0135102“Ocean-50” Grab0.1253.4Mud
25Sht 131-016April 5, 201655.8588518.95523104“Ocean-50” Grab0.24.0Fine sand
26Sht 131-020April 5, 201655.8176519.052195“Ocean-50” Grab0.1251.8Fine sand
27Sht 131-021April 5, 201655.8300319.1683575.7“Ocean-50” Grab0.253.9Fine sand
28Sht 132-002June 12, 201655.166519.83367Van Veen Grab0.056.9Fine silty mud
29Sht 132-003June 12, 201655.3768319.86791Van Veen Grab0.057.2Mud
30Sht 132-005June 13, 201655.3301720.5581729Van Veen Grab0.042.3Fine sand
31Sht 132-005June 13, 201655.3298320.55729Van Veen Grab0.042.2Fine sand
32Sht 132-008June 13, 201655.583520.0338375Van Veen Grab0.043.8Fine silty mud
33Sht 132-014June 15, 201655.7111719.3748372.5“Ocean-50” Grab0.12511.1Fine sand
34Sht 132-016June 15, 201655.7463319.4688371.4“Ocean-50” Grab0.4Sand, gravel, stones
35Sht 132-017June 15, 201655.791519.4306767.5“Ocean-50” Grab0.11.0Fine sand
36ANS 32-061August 5, 201655.3067517.7832777Van Veen Grab0.051.2Fine sand
37ANS 32-107August 7, 201655.5361815.319274Van Veen Grab0.15.1Mud
38ANS 32-108August 7, 201655.3336715.5774594Van Veen Grab0.13.5Mud
39ANS 32-203August 14, 201655.6095518.017367Van Veen Grab0.13.1Fine silty mud
40ANS 32-208August 26, 201655.4315520.3008342.2Van Veen Grab0.10.6Fine sand
41ANS 32-211August 29, 201655.5055520.2766250Van Veen Grab0.17.6Mixed medium or coarse sand
42ANS 32-227September 7, 201656.7073319.38575117“Ocean-50” Grab0.1251.2Mixed medium or coarse sand
43ANS 32-242September 8, 201657.3247819.86292215“Ocean-50” Grab0.1257.3Clayey mud
44ANS 32-284September 10, 201658.401120.38942120“Ocean-50” Grab0.1254.9Mud
45NORD-5October 27, 201654.9767320.2469720.7Van Veen Grab0.113.8Mixed medium or coarse sand
46NORD-6October 27, 201654.9774520.2567720.5Van Veen Grab0.215.7Mixed medium or coarse sand
47NORD-7October 27, 201654.9776820.2587519.8Van Veen Grab0.112.0Coarse silt
48NORD-8October 27, 201654.9882320.2632724Van Veen Grab0.216.1Mixed medium or coarse sand
49NORD-9October 27, 201654.9882720.2572219.5Van Veen Grab0.216.6Mixed medium or coarse sand
50NORD-10October 27, 201654.9851220.2352223Van Veen Grab0.217.6Mixed medium or coarse sand
51NORD-11October 27, 201654.9836320.2280222.8Van Veen Grab0.213.9Mixed medium or coarse sand
52NORD-12October 27, 201654.9920.2084825.1Van Veen Grab0.530.9Mixed medium or coarse sand
53ANS 33-060December 24, 201654.9901715.6421783“Ocean-50” Grab70.6Mud
Table 2

Number of pieces (fibres, films, and fragments) in sample and per kg dry weight (pcs per kg DW).

№ sampling stationsMass of analysed sample, gFragments, pcsFilms, pcsFibres, pcsCfragments, pcs per kg DWCfilms, pcs per kg DWCfibres, pcs per kg DWCtotal, pcs per kg DW
1300612882040293354
2400042901391103
34005718516222265503
440072524207168158
5400037560114172286
63001162093720698754
73003357910117264390
840021137633111150
9400013811906275411168
10400885225303398971266
1140012836388113204
124004925213339189541
134001151431014613961553
14400118661481088871142
154004218020104395519
16400161210715511610371308
1740030103311538127281
1840058285319293175460
194001810253884912311367
2040034546560893922610179
2140011009787727481528
2240032138312114261477
234003121761248710770
244001162281214720502209
2540007125038682721
264003279128311331
2740018271566497558719
284002177217142599758
294003124328130487646
3040049441227134173
3140041735114899158
32400273529103515647
33400723772480268373
341852235121243539804
35400191091173918271091
36400129684030228299
37400101690951528571104
384000611706913541424
394006161813810111431282
4040095373017124171
4140011644349135187
4240039601235232278
4340011331111371393
444001792591769326752943
454003141894355107
464006603819185117321
474001960149852736821040
484000303109396188
494000173005088138
5040042332127097179
514004374713116147276
5240022037763116186
534002675425263522837
Fig. 2

Analysis procedures: the modified NOAA method.

Fig. 3

Polymer samples.

Table 3

Polymer type and types of synthetic dyes identified using μ-Raman spectroscopy.

Polymer typeAcronym%Types of Synthetic Dyes (SD):
1Synthetic dyesSD47.2Hostasol-Green G-K
2PolyethylenePE/HDPE/LDPE11.1Irgazin Blue
3PolypropylenePP8.3Cobalt phthlocyanine
4Polymer blendPolymer blend5.6Terrae-Verte
5Polyethylene terephthalate/PolyesterPET/PES4.6Toloudine red
6PolydimethylsiloxanePDMS3.7Molybdenum oxide
7Cellulose/Cellulose acetateCE/CA3.7Titanium dioxide
8Polyvinyl chloridePVC2.8Cobalt sulphate
9Synthetic rubberSynthetic rubber1.9Motoperm Blue
10PolystyrenePS0.9Naples Yellow
11Methyl vinyl etherPVME0.9
12CarbonCarbon0.9
13Polymer methylpentenePMP0.9
14PlasticinePlasticine0.9
15NylonNylon0.9
16PolytetrafluoethylenePTFE0.9
17PolyviniledenePVDF0.9
18Poly (methyl 2-methylpropenoate)PMMA0.9
19PolymethacrylamidePMAM0.9
20VICRYL (polyglactin)VICRYL0.9
21Polyolefin elastomersPOE0.9
Fig. 4

Spectra of typical MPs identified by μ-Raman spectroscopy, the hit ratio between the specimen spectra and reference spectra (in percentages).

Study area and sampling stations*. * The maps were prepared with ArcGis 10.2.2 software, Natural Earth and HELCOM MADS spatial data. Depth contours from Ref. [4]. Expedition data, sampling sites locations and sediment characteristics. Number of pieces (fibres, films, and fragments) in sample and per kg dry weight (pcs per kg DW). Analysis procedures: the modified NOAA method. Polymer samples. Polymer type and types of synthetic dyes identified using μ-Raman spectroscopy. Spectra of typical MPs identified by μ-Raman spectroscopy, the hit ratio between the specimen spectra and reference spectra (in percentages). Detailed information on MPs content for each station is shown in Supplementary Material (Appendix 1) in Microsoft Excel format. Particle distribution by size and colour are provided in Microsoft Excel format in Appendix 2 and Appendix 3, respectively. Detailed results of μ-Raman spectroscopy are presented in Appendix 4.

Experimental design, materials, and methods

Sediment sampling

Sediment samples were collected at 53 stations in the Baltic Proper (Fig. 1) during six cruises of oceanographic research vessels and two expeditions on small boats in the coastal zone. Ordered by time, the cruises are: (1) boat (July 3, 2015); (2) boat (October 9, 2015); (3) RV NORD (cruise NORD March 30, 2016); (4) RV Professor Shtokman (cruise Sht 131: March 31 - April 5, 2016); (5) RV Professor Shtokman (cruise Sht 132: June 12–15, 2016), (6) RV Akademik Nikolay Strakhov (cruise ANS 32 August 5 - September 10, 2016); (7) RV NORD (cruise NORD October 27, 2016); (8) RV Akademik Nikolay Strakhov (cruise ANS 33 December 24, 2016) (Table 1). The sampling of the upper 5–7 cm of bottom sediments was performed at the depths from 3 m to 215 m using different sampling tools: (i) a hand-operated drag with mouth size of 200 × 100 mm (8 samples), (ii) a Van Veen grab (0.1 m2) (24 samples), and (iii) an “Ocean-50” grab (0.25 m2) (21 samples). The sampled bottom deposits had different grain sizes ranging from clayey mud to mixed medium or coarse sand and gravel with stones [5]. The mass of an individual sample varied from 0.4 kg to 70 kg. All the samples were stored and transported in a closed metallic bucket or can and were homogenized prior to handling in the laboratory with a steel mixer. The buckets containing samples were stored at room temperature until analysis, and clean stainless-steel spoons were used for removing samples from the bucket.

Methods

Sample preparation

Microplastics were extracted from the sediment samples using the method employed by Ref. [1] with modifications [2,3]. To maximize extraction rates, sediments with high clay content were washed through a sieve cascade (0.333 μm, 174 μm, 174 μm) before the extraction to remove clayey mud fractions, which hampers the extraction process [3]. The sediment retained by the sieves was subjected to flotation (Fig. 2). In brief, the modified NOAA method consists of the following main steps [2,3]: (1) Multiple MPs extraction from a sediment sample by means of density separation with the ZnCl2 solution (specific density 1.6 g mL−1), (2) Filtering of supernatant solution above the sediment with the filter funnel, (3) Wet peroxide oxidation on the water bath, (4) Calcite fraction digestion with HCl solution, (5) Filtering with filter funnel, (6) Density separation to detach oxidized organic matter, (7) Filtering with filter funnel, (8) MPs detection with a stereomicroscope, and additionally (9) MPs identification with a Raman spectrometer (Fig. 2).

Analytical techniques

The MP particles were optically analysed and photographed using a stereomicroscope (Micromed MC2 Zoom Digital) with magnification from ×10 to ×40 directly on the filter surface according to recommendations for microscopic determination [6]. All the analysis and detection procedures were performed by the single operator to exclude inter-operator variability. Since plastics particles cannot be fully exactly identified only by visual observation [[7], [8], [9], [10], [11]], μ-Raman spectroscopy was used to verify the result and attain the composition of plastic-like particles [12]. Raman Centaur U (LTD «NanoScanTechnology», Russia) spectrometer was used to obtain plastic spectra [13].

Contamination control and quality analysis

Metal laboratory equipment and glass tableware were used where possible to minimize external contamination. All instruments used during the extraction process were washed with distilled water and dried before the analysis. Cotton lab coats and clothing from non-synthetic materials were used to minimize airborne contamination during samples handling and extraction. Twelve blank samples were run to assess the level of background contamination according to Ref. [3]. As an additional measure to control the extraction efficiency, artificial reference particles (ARPs) were added to each sample prior to the extraction procedure. Rectangular ARPs with the side dimension of 0.88 ± 0.41 mm (p = 0.05; n = 40) were prepared from a sheet of fluorescent PET 0.46 mm ± 0.02 mm thick (p = 0.05; n = 40). These ARPs, with their artificial shape and characteristic fluorescence, are easily distinguishable from MPs of natural sediments, and provide a clear indication of the quality of the extraction procedure [3].

Classification methods

A visual assessment was performed to identify the shape, size, and colour of MPs according to the physical characteristics of the particles. The extracted MPs were classified into three groups: fragments, films, and fibres according to Ref. [14]. Particle colour was divided into the following categories: transparent, white, green, blue, yellow, red, brown, and black, which is close to categories according to Refs. [8,15]. The blue category included deep blue, light blue, and violet particles. The yellow category also included orange particles. The transparent category included colourless and muddy particles. The red category also included pink and purple particles. The black category included transparent black and grey particles. The extracted particles were divided into 24 categories using similarity of their visual appearance (shapes, colours), mechanical quality (rigid, soft, elastic, foamed, etc.), and behaviour during a hot-needle test.

μ-Raman spectroscopy verification

The analysis procedure followed [13]. Out of the identified MPs, the core polymer type of some specimens was impossible to identify because of the strong signal induced by synthetic dyes (SD) or strong background fluorescence. Still, the fact of presence of SD was considered as confirmation of synthetic origin of a particle. So, all such specimens were accounted as MPs (for example, Fig. 3). Polymer type and types of synthetic dyes identified using μ-Raman spectroscopy are presented in Table 3. In other cases, the identification by μ-Raman spectroscopy was not possible due to too small particle size or chemical compounds remaining on the surface of a particle. Raman spectra of top 8 typical MPs are presented in Fig. 4.

Specifications Table

SubjectEnvironmental Science, Ecology
Specific subject areaMicroplastic Contamination, Environment
Type of dataTableChartGraphFigure
How data were acquiredVan Veen and “Ocean-50” grab samplers, hand-operated drag;NOAA extraction; Stereomicroscope (Micromed MC2 Zoom Digital); Raman Centaur U (LTD “NanoScanTechnology”, Russia) spectrometer.
Data formatRaw and Analysed.
Parameters for data collectionSampling of bottom sediments. Microplastics extraction according to the modified NOAA method [[1], [2], [3]]. Contamination control. Microscopy and μ-Raman spectroscopy analyses.
Description of data collectionData of number of pieces per kg dry weight (0.2–5 mm, MPs) in bottom sediments from 3 to 215 m depth on the base of 53 samples obtained in 8 cruises of research vessels in the Baltic Sea in 2015–2016. Map of study area and sampling stations. Distribution of MPs by size and by colour. Raw μ-Raman spectroscopy intensity.
Data source locationThe Baltic Sea (Gotland, Gdansk and Bornholm basins), 53 stations. Locations of the 53 station are on URL: http://lamp.ocean.ru/index.php/2016/11/18/samples-map/
Data accessibilityAll data is accessible within this article.
Value of the Data

Microplastic contamination in bottom sediments of the Baltic Sea Proper in 2015–2016 is documented.

A benchmark for future studies dedicated to microplastic contamination in the Baltic Sea is presented.

Obtained data can be used for comparative analysis of plastic contamination in bottom sediments of other seas and oceans.

Number of pieces per kg dry weight, spatial distribution, types of particles (fibres, films, fragments), as well as size, colour, and plastic types are reported.

  7 in total

Review 1.  Microplastics in the marine environment: a review of the methods used for identification and quantification.

Authors:  Valeria Hidalgo-Ruz; Lars Gutow; Richard C Thompson; Martin Thiel
Journal:  Environ Sci Technol       Date:  2012-03-02       Impact factor: 9.028

2.  Microplastics in Baltic bottom sediments: Quantification procedures and first results.

Authors:  M Zobkov; E Esiukova
Journal:  Mar Pollut Bull       Date:  2016-10-31       Impact factor: 5.553

Review 3.  Identification of microplastics using Raman spectroscopy: Latest developments and future prospects.

Authors:  Catarina F Araujo; Mariela M Nolasco; Antonio M P Ribeiro; Paulo J A Ribeiro-Claro
Journal:  Water Res       Date:  2018-06-06       Impact factor: 11.236

4.  Microplastics in offshore sediment in the Yellow Sea and East China Sea, China.

Authors:  Chunfang Zhang; Hanghai Zhou; Yaozong Cui; Chunsheng Wang; Yanhong Li; Dongdong Zhang
Journal:  Environ Pollut       Date:  2018-10-25       Impact factor: 8.071

5.  Microplastic abundance, distribution and composition in the Pearl River along Guangzhou city and Pearl River estuary, China.

Authors:  Muting Yan; Huayue Nie; Kaihang Xu; Yuhui He; Yingtong Hu; Yumei Huang; Jun Wang
Journal:  Chemosphere       Date:  2018-11-14       Impact factor: 7.086

Review 6.  Microplastics in the environment: Challenges in analytical chemistry - A review.

Authors:  Ana B Silva; Ana S Bastos; Celine I L Justino; João P da Costa; Armando C Duarte; Teresa A P Rocha-Santos
Journal:  Anal Chim Acta       Date:  2018-02-20       Impact factor: 6.558

7.  Microplastic content variation in water column: The observations employing a novel sampling tool in stratified Baltic Sea.

Authors:  M B Zobkov; E E Esiukova; A Y Zyubin; I G Samusev
Journal:  Mar Pollut Bull       Date:  2018-11-23       Impact factor: 5.553

  7 in total
  2 in total

1.  From macro to micro: dataset on plastic contamination along and across a sandy tide-less coast (the Curonian Spit, the Baltic Sea).

Authors:  Elena Esiukova; Liliya Khatmullina; Olga Lobchuk; Alexey Grave; Alexander Kileso; Mirco Haseler; Andrey Zyubin; Irina Chubarenko
Journal:  Data Brief       Date:  2020-04-30

2.  Characterization of Collagen from Three Genetic Lines (Gray, Red and F1) of Oreochromis niloticus (Tilapia) Skin in Young and Old Adults.

Authors:  Nataly Reátegui-Pinedo; David Salirrosas; Linda Sánchez-Tuesta; Claudio Quiñones; Segundo R Jáuregui-Rosas; Gabriela Barraza; Angelita Cabrera; Carmen Ayala-Jara; Renata Miliani Martinez; André Rolim Baby; Zulita Adriana Prieto
Journal:  Molecules       Date:  2022-02-08       Impact factor: 4.411

  2 in total

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