An 18S V4 rRNA metabarcoding dataset of protist diversity in the Atlantic inflow to the Arctic Ocean, through the year and down to 1000 m depth
Arctic marine protist communities have been understudied due to challenging sampling conditions, in particular during winter and in deep waters. The aim of this study was to improve our knowledge on Arctic protist diversity through the year, in both the epipelagic (< 200 m depth) and mesopelagic zones (200–1000 m depth). Sampling campaigns were performed in 2014, during five different months, to capture the various phases of the Arctic primary production: January (winter), March (pre-bloom), May (spring bloom), August (post-bloom), and November (early winter). The cruises were undertaken west and north of the Svalbard archipelago, where warmer Atlantic waters from the West Spitsbergen Current meet cold Arctic waters from the Arctic Ocean. From each cruise, station, and depth, 50 L of seawater was collected, and the plankton was size-fractionated by serial filtration into four size fractions between 0.45–200 µm, representing picoplankton (0.45–3 µm), small and large nanoplankton (3–10 and 10–50 µm, respectively), and microplankton (50–200 µm). In addition, vertical net hauls were taken from 50 m depth to the surface at selected stations. The net hauls were fractionated into the large nanoplankton (10–50 µm) and microplankton (50–200 µm) fractions. From the plankton samples DNA was extracted, the V4 region of the 18S rRNA-gene was amplified by polymerase chain reaction (PCR) with universal eukaryote primers, and the amplicons were sequenced by Illumina high-throughput sequencing. Sequences were clustered into amplicon sequence variants (ASVs), representing protist genotypes, with the dada2 pipeline. Taxonomic classification was made against the curated Protist Ribosomal Reference database (PR2). Altogether, 6536 protist ASVs were obtained (including 54 fungal ASVs). Both ASV richness and taxonomic composition varied between size fractions, seasons, and depths. ASV richness was generally higher in the smaller fractions and higher in winter and the mesopelagic samples than in samples from the well-lit epipelagic zone during summer. During spring and summer, the phytoplankton groups diatoms, chlorophytes, and haptophytes dominated in terms of relative read abundance in the epipelagic zone. Parasitic and heterotrophic groups such as Syndiniales and certain dinoflagellates dominated in the mesopelagic zone all year, as well as in the epipelagic zone during the winter. The dataset is available at https://doi.org/10.17882/79823 (Egge et al., 2014).
The West Spitsbergen Current is considered the main gateway from the Atlantic into the Arctic Ocean, as it flows along the west side of the Svalbard Archipelago, transporting relatively warm and salty water (T>2 ∘C, S>34.92; see Randelhoff et al., 2018) into the Barents Sea and Arctic Ocean (Fig. 1). In response to global warming, this current has become both warmer and stronger in recent years, increasingly replacing water advected from the central Arctic Ocean with warm and salty water of Atlantic origin, a process referred to as “Atlantification” (Årthun et al., 2012). This increase in oceanic heat in the Arctic area correlates with the rapid decline in ice extent observed over the past decades (Årthun et al., 2012). Increased inflow of Atlantic water affects the primary production and protist communities in several ways. Water mixing happens more easily in the Atlantic water, because in contrast to the permanently salinity-stratified central Arctic Ocean, the water column is temperature-stratified and less stable; thus upper-ocean nutrients are more efficiently replenished early in winter. Furthermore, the warm Atlantic water melts the ice, and a layer of fresh, cold water is formed near the surface. The timing of this stratification is crucial for the onset of the spring bloom, and thinner ice means decreased light limitation for the algae living inside and under the ice. However, the loss of sea ice also results in the loss of habitat for many protists, especially those adapted to a life in or on the ice. These various effects of climate change may thus alter both the location and timing of blooms, as well as their biomass and species composition (e.g., Eamer et al., 2013; Li et al., 2009).
To understand what consequences environmental changes in this Arctic region will have for the biodiversity of the whole pelagic community and for the production through the food web up to higher trophic levels, we need to know what the community components are and where and when the organisms occur. This will also enable us to detect future changes. However, still relatively little is known about the diversity and distribution of protists in the Arctic Ocean (e.g., Lovejoy, 2014). Arctic winter microbial eukaryote communities are particularly understudied due to logistic challenges, which include ice cover and frequent storms. Metabarcoding using high-throughput sequencing has become a commonly used method to study the community composition of marine protists and has revealed a huge unknown diversity (e.g., de Vargas et al., 2015). In recent years, several metabarcoding studies of protist communities in the Arctic Ocean have been undertaken, but most represent only snapshots of the community as based on a single cruise or season (e.g., Bachy et al., 2011; Kilias et al., 2014; Monier et al., 2015; Vader et al., 2015). Studies that have sampled the full yearly cycle have typically only sampled the upper water column (0–50 m depth) (e.g., Marquardt et al., 2016).
Here we present a metabarcoding dataset from the northern Svalbard region of the Arctic Ocean sampled during five cruises representing the full seasonal cycle and at three to four depths from the surface down to 1000 m. Metabarcoding targeted the V4 region of the 18S rRNA gene. The data are provided both as raw reads and as amplicon sequence variants obtained after processing with the dada2 pipeline, with corresponding ASV abundance tables. The data presented here were obtained within the framework of the project “MicroPolar” (https://www.researchinsvalbard.no/project/7280, last access: 30 August 2021). The virus and prokaryote communities from the same project have been described in Sandaa et al. (2018) (virus) and Wilson et al. (2017) and Paulsen et al. (2016) (prokaryote). Environmental data from the MicroPolar sampling campaign have previously been published in Paulsen et al. (2017) and Randelhoff et al. (2018). A subset of the environmental data corresponding to the stations and depths of the protist metabarcoding samples is included in the data repository of the present study (https://doi.org/10.17882/79823, Egge et al., 2014).
The physical and biogeochemical oceanographic conditions during these cruises have previously been described in detail in Randelhoff et al. (2018). Flow-cytometric counts of viruses, bacteria, and pico- and nanoplankton have been published in Sandaa et al. (2018). We briefly describe the methods and reiterate the main results here to provide background for our metabarcoding data. The complete dataset from Randelhoff et al. (2018) can be found at the PANGAEA Data Publisher for Earth and Environmental Science (https://doi.org/10.1594/PANGAEA.884255, Paulsen et al., 2017). The reader is advised to consult the original papers for detailed descriptions of the methods. The environmental parameters included here are listed in Table 1.
2.1 Study area
Sampling campaigns were performed in 2014 as described in Paulsen et al. (2017), Wilson et al. (2017), Randelhoff et al. (2018), and Sandaa et al. (2018), during five different months, to capture the various stages of the Arctic primary production: January (6–15 January, winter), March (5–10 March, pre-bloom), May (15 May–2 June, spring bloom), August (7–18 August, post-bloom), and November (3–10 November, early winter). The cruises were undertaken west and north of the Svalbard archipelago, where warmer Atlantic water in the West Spitsbergen Current meets colder water from the Arctic Ocean (Fig. 1). Bottom depth varied from 327 m (November station N03) to c. 3000 m (March station M05). The area and locations for each sampling campaign were as similar as possible, but constrained by the sea ice cover, from 79 to 82.6∘ N. During each cruise, transects of three to six stations were sampled at three or four depths: in the epipelagic zone at 1 m and at the deep chlorophyll maximum (usually between 15–25 m) and in the mesopelagic zone at one or two depths, as a rule 500 and 1000 m, or as deep as the bathymetry of the station permitted.
2.2 Environmental conditions
2.2.1 Day length and euphotic zone depth
Day length at each cruise and station was calculated with the “daylength” function in the “geosphere” R package Hijmans (2019). Day length was 0 h during winter (January, November), 6–8 h in March, and 24 h in May and August. Continuous profiles of photosynthetically available radiation (PAR; radiation at wavelengths between 400 and 700 nm) in the upper ocean were measured during the May and August cruises using a RAMSES radiometer (TriOS, Germany) with a wavelength spectrum of 190–575 nm. The euphotic zone depth (Zeu) was then defined as the depth at which downwelling PAR reached 1 % of its value just below the surface. Euphotic zone depth was 19–23 m in May, 22 m in August at station P05, and 48 and 45 m at stations P06 and P07, respectively. The uncertainty of these values is 2–3 m (Randelhoff et al., 2018).
2.2.2 Ice cover
The ice extent was smallest in January and peaked in May (see Fig. 1 in Wilson et al., 2017). The two stations sampled in January were in the open ocean, whereas in March, May, and August, all the stations were situated in varying degrees of drift ice, except March station M06 and August station P05, which were situated in open water. In November, all stations were in open water, except November station N02, which was in open drift ice (see Wilson et al., 2017, for the definition of the different ice types).
2.2.3 Hydrographical conditions
Vertical profiles of temperature, salinity, and fluorescence were recorded at each sampling station using an SBE 911plus CTD system (Sea-Bird Scientific USA, Bellevue, WA, USA). Conditions were dominated by the large-scale inflow of warm Atlantic water (the West Spitsbergen Current), which is modified as it enters the cold Arctic Ocean. Surface temperature was highest in August, station P05, ≃ 6 ∘C. Surface temperature and salinity were generally lower at the stations farther off the slope compared to those on the shelf slope (Fig. 2). The difference between stations diminished by depth, and at 1000 m the conditions were almost identical across stations and months (Fig. 2).
2.2.4 Inorganic nutrients and chlorophyll a
Water samples for nutrients and chl a were taken with 8 L Niskin bottles mounted on a General Oceanics 12-bottle rosette. Nutrients (NO +NO, Si(OH)4, PO) were frozen until analysis and analyzed by standard seawater methods using a Flow Solution IV analyzer from O.I. Analytical, USA. Atlantic water was the dominant source of nutrients (as indicated by ; see Randelhoff et al., 2018). In the surface, inorganic nutrients and chl a were inversely related to each other (Fig. 2). As expected, chl a concentrations were close to zero in the dark winter months (November and January). In March, there was some daylight, but the water column was not yet stratified, which prevented initiation of the spring bloom. Chl a concentrations peaked in May (at most 14 µg L−1), concomitantly with depletion of inorganic nutrients. From May to August chl a concentration decreased to < 5 µg L−1, while the concentrations of inorganic nutrients were still generally low. By November, the concentrations of inorganic nutrients in the epipelagic zone had increased and were again back to the levels observed in January and March.
2.2.5 Cell counts
FCM analyses were performed using an Attune Focusing Flow Cytometer (Applied Biosystems by Life Technologies) with a syringe-based fluidic system and a 20 mW 488 nm (blue) laser. The samples were fixed with glutaraldehyde (0.5 % final conc.) at 4 ∘C for a minimum of 30 min, flash-frozen in liquid nitrogen, and stored at −80 ∘C until analysis. Autotrophic phytoplankton was categorized as the cyanobacterium Synechococcus, picophytoplankton, or nanophytoplankton, based on variation in side scatter, chlorophyll a, and phycoerythrin autofluorescence. Samples for enumeration of virus-like particles, heterotrophic prokaryotes, and nanoflagellates were stained with SYBR Green I and distinguished based on side scatter and green fluorescence. Virus-like particles were categorized as “small”, “medium”, and “large”, based on fluorescence intensity. Cell counts of pico- and nanophytoplankton, heterotrophic nanoflagellates, Synechococcus, and heterotrophic prokaryotes were generally higher in May and August than during winter and early spring and higher in the epipelagic than the mesopelagic samples. Virus counts were generally higher in January and August than the other months, and the variation by depth was smaller than for prokaryotes and eukaryotes (cf. Figs. 3 and 4 in Sandaa et al., 2018).
3.1 Sample preparation for DNA extraction
3.1.1 Niskin bottles
From each station and depth, 50 L of seawater was collected in 8–10 L Niskin bottles, mounted on a General Oceanics 12-bottle rosette deployed from the vessels. To acquire enough water for the samples described herein, in addition to other biological and physicochemical samples as mentioned above, two casts were usually made per station: one from each of the epi- and mesopelagic zones. The samples were size fractionated. All equipment for filtration and size fractionation was rinsed twice with dH2O between each sample. During the January and March cruises, the samples were prefiltered through a 180 µm mesh size nylon filter and size-fractionated into the 3–180 and 0.45–3 µm fractions by filtration using a peristaltic pump (Masterflex 07523-80, Cole-Parmer, IL, USA), through serially connected 3 and 0.45 µm polycarbonate filters (Isopore/Durapore, 142 mm diameter, Millipore, Billerica, MA, USA), mounted in stainless-steel tripods (Millipore). The filters were removed from the filter holders and cut in four. Two of the pieces were used for DNA extraction, and the others were saved for other purposes. The pieces for DNA were transferred to a 50 mL Falcon tube with 1 mL (65 ∘C) AP1 lysis buffer (Qiagen, Hilden, Germany), the plankton material was washed off the filters, and buffer with material and the filters were transferred to two separate cryovials. AP1 buffer (65 ∘C) was added to the vial with the filters, flash-frozen in liquid nitrogen, and kept at −80 ∘C until DNA extraction. During the May, August, and November cruises the water was sequentially filtered through 200, 50, and 10 µm nylon mesh. The material on each nylon mesh was collected with sterile filtered seawater in a 50 mL Falcon tube and collected by filtration on a polycarbonate filter (10 µm pore size 47 mm diameter, Millipore). The filters were transferred to cryovials to which 1 mL of warm AP1 buffer was added, flash-frozen in liquid nitrogen and kept at −80 ∘C until DNA extraction. The size fraction < 10 µm passing through the nylon mesh system was fractionated into the 3–10 and 0.45–3 µm size fractions by serial filtration through 142 mm diameter polycarbonate filters as described above.
3.1.2 Net hauls
Vertical phytoplankton net hauls (mesh size 10 µm) were collected between 50 m depth and the surface at each station in May, August, and November. The net haul samples were diluted to 1 L with sterile filtered seawater and size fractionated by filtration through 200, 50, and 10 µm nylon mesh. The plankton was washed off the nylon mesh with sterile seawater, diluted to 50 mL in a Falcon tube and a 20 mL aliquot collected on a 10 µm pore size polycarbonate filter, and preserved for DNA extraction as described above. The remaining 30 mL was preserved for microscopical analyses to be reported separately. An overview of which types of samples and size fractions are available from each cruise can be found in Table 2.
3.2 DNA extraction
DNA was extracted with the DNeasy Plant mini kit (Qiagen), according to the protocol from the manufacturer, except for the following step: to disrupt the thick cell walls of certain protist groups, the frozen samples in cryovials were incubated at 95 ∘C for 15 min and then shaken in a bead-beater 2× 45–60 s. Subsequently, 4 µL RNase was added, and the lysate was incubated on a heating block at 65 ∘C for 15–20 min, with vortexing in between. Purity and quantity of the extracted DNA was assessed with NanoDrop.
4.1 PCR amplification and Illumina sequencing
The V4 region of the 18S rRNA gene was amplified with the primer pair 18S TAReuk454FWD1 (5'-CCAGCASCYGCGGTAATTCC-3') and V4 18S Next.Rev (5'-ACTTTCGTTCTTGATYRATGA-3') (Piredda et al., 2017), which yields a fragment of 410–420 base pairs. This primer pair is an improvement over the widely used primers developed by Stoeck et al. (2010), which have been used in more than 60 studies. The Piredda primers aim to reduce the biases against Haptophyta seen in the Stoeck primers (Piredda et al., 2017). The samples were prepared for Illumina sequencing with a so-called dual-index approach (e.g., Fadrosh et al., 2014), where a 12 bp internal barcode was added to both the forward and reverse amplification primers for the initial amplification. In order to pool several samples into one library preparation, 19 unique barcodes for each direction were used. The internal barcodes were designed to give a balanced distribution of the four bases, following the recommendations of Fadrosh et al. (2014). Polymerase chain reactions (PCRs) consisted of 12.5 µL KAPA HiFi HotStart ReadyMix 2× (KAPA Biosystems, Wilmington, MA, USA), 5 µL of each primer (1 µM) and 10 ng DNA template and PCR-grade water to a final volume of 25 µL. The PCR was run on an Eppendorf thermocycler (Mastercycler, ep gradient S, Eppendorf), with an initial denaturation step at 95 ∘C for 3 min, followed by 25 cycles of denaturation at 98 ∘C for 20 s, annealing at 65 ∘C for 60 s, and elongation at 72 ∘C for 1.5 min, with a final elongation step at 72 ∘C for 5 min. The reactions were performed in triplicate for each sample and pooled prior to purification and quantification. The length of the PCR products was assessed by gel electrophoresis. In all samples, there was a strong band at about 470 bp and no other bands (data not shown). The PCR products were purified with AMPure XP beads (Beckman Coulter, Brea, USA) using the standard protocol with elution buffer EB (Qiagen), quantified with a Qubit dsDNA High-Sensitivity kit (Thermo Fisher, Waltham, MA, USA) and pooled in equal concentrations to create nine pools with ca. 19 samples in each. The pools were sent to library preparation at the Norwegian Sequencing Centre (Oslo, Norway) and GATC GmbH (Constance, Germany) with the KAPA library amplification kit (Kapa Biosystems). Further quality control of the amplicons was carried out with Bioanalyzer at the sequencing centers prior to Illumina sequencing. Due to worldwide supply problems with the Illumina MiSeq chemistry in 2015, the sequencing was done with a modified HiSeq protocol on two HiSeq runs at the GATC in October 2015. This modified protocol yielded 250 bp paired-end reads. The HiSeq sequencing runs were spiked with 20 % PhiX (viral DNA added to ensure homogeneity of bases during sequencing). To assess variation between DNA extracts and annealing temperature, we separately sequenced replicate DNA extractions and replicate PCR runs with 60 ∘C annealing temperature for a few samples (indicated in Table 3). After initial analysis of the HiSeq data, samples with low numbers of reads were re-amplified with 30 cycles with the original DNA as template to increase the concentration of the PCR product and re-sequenced with Illumina MiSeq at the Norwegian Sequencing Centre. The MiSeq protocol yielded 300 bp paired-end reads. In total, we sequenced 199 samples separately. The taxonomic composition of sequencing replicates of the same sample was inspected visually, and in all cases the different sequencing protocols were found to give similar taxonomic compositions.
4.2 Bioinformatics processing
PhiX sequences were removed, and the raw reads were sorted according to the Illumina index by the Illumina software at the sequencing provider. For the HiSeq datasets, the samples within each Illumina library were demultiplexed with cutadapt v2.10 with Python 3.6.11 (Martin, 2011), requiring 0 errors in the internal barcodes. The amplification primers were removed with cutadapt v2.8 with Python 3.7.6, with setting
--trim-n (trim N's on ends of reads).
The reads were denoised and merged with dada2, v1.16 (Callahan et al., 2016). For the HiSeq reads the settings were
truncLen = c(240,200), minLen = c(240, 200), truncQ = 2, maxEE = c(10, 10), and max_number_asvs = 0. Chimeras were detected with isBimeraDenovo with default settings and removed with removeBimeraDenovo, with
“method_chimera” = “pooled”. For the MiSeq reads truncLen and minLen were set to c(270, 240), and the other settings were the same as for HiSeq. The reads were subsequently classified with assignTaxonomy, the dada2 implementation of the naive Bayesian classifier method (Wang et al., 2007), against the Protist Ribosomal Reference Database, version 4.12.0 (https://github.com/pr2database/pr2database/releases/tag/v4.12.0, last access: 25 January 2021; Guillou et al., 2013). ASVs with less than 90 % bootstrap value at class level and/or which comprised fewer than 10 reads in total were removed. As this study is focusing on the protists, all reads assigned to Metazoa and Viridiplantae (Embryophyceae) were excluded from the processed ASV tables (Table 4).
4.3 Preparation of ASV tables
Preparation of the ASV tables was done in R v. 3.6.0 (R Core Team, 2019). To be able to compare ASV richness between samples (i.e., the number of ASVs in each sample), the DNA samples were subsampled to equal read number. Prior to subsampling, data from fastq files that map onto the same size-fractionated DNA sample were merged by taking the sum of the read number for each ASV. The merging was done to increase the number of reads in the samples that initially had a low read number after HiSeq sequencing. The DNA samples were subsampled according to size fraction as follows: 0.45–3 µm: 40 000 reads; 3–180 µm: 88 000 reads; 3–10 µm: 40 000 reads; 10–50 µm: 40 000 reads; and 50–200 µm: 8 000 reads. It should be noted that the number of reads in the 3–180 µm fraction samples was in some cases lower than the subsample size. Subsampling to equal read number was performed 100 times, and the average read number per ASV was used, rounded to 0 decimals. Subsampling was done with the function rrarefy() from the “vegan” package (Oksanen et al., 2020), v. 2.5-7. The low number of protist reads in the 50–200 µm fraction was due to a high proportion of Metazoan reads in this fraction. To calculate the ASV richness of each sample, the subsampled ASV table was transformed to presence–absence. An overview of the available versions of the ASV table is given in Table 4. To assess whether the sequencing depth was sufficient, we plotted rarefaction curves for each DNA sample and calculated the slope at the endpoint of the curve with the functions “rarecurve” and “rareslope” respectively. Figures were made with the R package “ggplot2” (Wickham, 2016). In addition to the figures and tables presented in the paper, interactive versions of figures, tables, and supplementary material are available as a Shiny app (Chang et al., 2019) (available at https://micropolar-protists.metapr2.org/, last access: 20 September 2021). Interactive figures and tables were made with the packages “DT” (Xie et al., 2020) and “plotly” (Sievert, 2020), respectively.
5.1 Overview of sequenced samples
In total we obtained 44 water samples from Niskin bottles and 8 net hauls, which were fractionated into 140 and 15 size-fractionated samples, respectively (the DNA isolation of the 10–50 µm fraction from the net haul taken at station P04 in May failed). The samples from Niskin and net hauls are referred to as DNA samples in the following, and they are denoted month_station_depth_minfract_maxfract or month_station_net_minfract_maxfract, respectively. On some DNA samples, we performed replications of DNA extraction, PCR with variable annealing temperature, and/or replicate sequencing. Thus, one or more fastq-file pairs can map onto the same DNA sample. The fastq files were deposited individually to the European Nucleotide Archive (ENA, project accession number PRJEB40133) and are referred to as a “sequencing event” (“seq_event”) in Table 3). In total the dataset consists of 199 sequencing events, some of which were merged, to form in total 155 DNA samples. Description of metadata available for each fastq-file pair can be found in Table 3. Table 1 describes all environmental parameters obtained from each water acquisition event (i.e., from the Niskin samples). These are referred to as “env_sample” and labeled month_station_depth.
5.2 Total number of reads and ASVs
After quality filtering, dada2 processing, removal of chimeras, and non-target taxonomic groups, the dataset comprised 6536 protist ASVs, corresponding to 32 164445 reads. After subsampling to equal number of reads per sample within each size fraction, the dataset was reduced to 6430 ASVs and 5 729 358 reads. Number of ASVs per division or class within each size fraction, after subsampling, is shown in Table A1. In total, we recovered 3339, 2720, 2799, 1153, and 3172 ASVs in the 0.45–3, 3–10, 10–50, 50–200, and 3–180 µm size fractions, respectively. Note that the numbers are not directly comparable, as the fractions were not obtained from the same number of samples (e.g., 3–180 µm were only sampled in January and March). Syndiniales and Dinophyceae had the highest number of assigned ASVs, with 2166 and 1723, respectively. Ciliophora, Bacillariophyta, Radiolaria, and Chlorophyta had between 400 and 200 assigned ASVs each (Table A1).
5.3 Sample saturation
Slopes of rarefaction curves at the endpoint, after subsampling, ranged from 0 to 0.014 (Fig. 3), which means that for every 1000 extra reads sequenced, we could expect to find between 0 and 14 new ASVs (de Vargas et al., 2015). There was no correlation between the number of ASVs detected in a sample and the slope of the rarefaction curve (, p=0.11), which means that the DNA samples with a low number of ASVs were not necessarily undersampled.
5.4 Variation in taxonomic composition by season, depth, and size fraction
The proportional taxonomic composition of the metabarcoding reads, at division or class level, is shown in Fig. 4. The taxonomic composition of the ASV richness in each sample is shown in Fig. A1. The metabarcoding data reveal variation in taxonomic composition by both season and depth, in all size fractions. In the following, the fractions are defined as follows: 0.45–3 µm is picoplankton, 3–180 µm is nano-micro, 3–10 µm is small nanoplankton, 10–50 µm is large nanoplankton, and 50–200 µm is microplankton. All the major protist groups varied from less than 1 % of the reads to up to 99 % for the most abundant (e.g., Syndiniales in the picoplankton fraction and diatoms in the microplankton fractions; Table A2).
In January (winter) and March (pre-bloom), heterotrophic or parasitic groups (e.g., certain dinoflagellates, Syndiniales, and Picozoa) were dominating at all depths. In the picoplankton size fraction, the parasitic dinoflagellate group Syndiniales had the highest relative abundance these months, with up to 99 % of the reads, followed by the heterotrophic group Picozoa, with up to 35 % of the reads, and Pseudofungi with up to 12 % (previously categorized as marine stramenopiles, MAST). Syndiniales also had the highest ASV richness in all samples. In the nano-micro fraction, Dinophyceae had generally higher relative abundance, with 20 %–55 % of the reads in most samples. Syndiniales and Picozoa had up to 82 % and 40 %, respectively. Syndiniales also had the highest ASV richness in this fraction, followed by Dinophyceae. Other heterotrophic groups notably present in this fraction were Pseudofungi and Radiolaria, with 2 %–20 % of the reads each, and Ciliophora and Choanoflagellida with up to 6 % of the reads. ASVs assigned to phototrophic groups (e. g. diatoms, haptophytes, and chlorophytes) were detected in these months but constituted less than 3 % of the reads in all samples.
The May samples were characterized by higher proportions of phototrophs in all size fractions. In the pico- and small nanoplankton fractions, there was a pronounced difference between the epipelagic and mesopelagic samples this month. In the picoplankton fraction, Chlorophyta (mainly represented by the genera Micromonas and Bathycoccus) had high relative abundance in the epipelagic samples, with 17 %–43 % of the reads. In the small nanoplankton fraction, Haptophyta (mainly represented by the genus Phaeocystis) and Dinophyceae were the most abundant groups in the euphotic samples with 25 %–47 % and 14 %–39 % of the reads, respectively. The mesopelagic samples in the pico- and small nanoplankton fractions were characterized by a high abundance of Syndiniales, with 47 %–85 % of the reads. In these fractions, ASV richness was generally higher in the mesopelagic than in the epipelagic samples. Syndiniales generally had the highest number of ASVs, despite having lower relative abundance. In the large nanoplankton and microplankton fractions, diatoms were dominating in both the epi- and mesopelagic samples, with up to 99 % of the reads. Dinoflagellates (Dinophyceae) was the second most abundant group in the large nanoplankton fraction, with up to 50 % of the reads. In the microplankton fraction, Phaeocystis was also abundant in certain samples, with up to ca. 30 % of the reads. In the net haul samples from May, the diatoms were dominating with up to 97 % of the reads. Dinophyceae had 10 %–11 %, and Haptophyta constituted 11 % in the microplankton fraction from station P01. These fractions generally had lower ASV richness than the pico- and nanoplankton, and there was no clear difference in ASV richness by depth. The groups with the highest ASV richness in these samples were Dinophyceae, Bacillariophyta, and Syndiniales.
In August, in the picoplankton fraction of the epipelagic samples, Dinophyceae had the highest relative abundance, with 13 %–64 %. Haptophyta had ca. 4 %–14 % and Chlorophyta ca. 7 %–25 % in these samples. In the mesopelagic samples in this fraction, Syndiniales also dominated in August, with up to 68 % of the reads. Radiolaria accounted for 10 %–13 % of the reads in these samples, whereas Picozoa had 3 %–15 %. Picozoa relative abundance also reached up to 12 % in the epipelagic samples. In the nanoplankton size fraction, Dinophyceae was dominating, with 27 %–79 % of the reads. Similar to in May, Syndiniales generally had the highest ASV richness in the picoplankton fraction. In the nanoplankton fraction, Syndiniales and Dinophyceae had similar ASV richness. In the large nanoplankton fraction, Dinophyceae dominated with 31 %–88 % of the reads. Diatoms constituted up to 41 % of the reads, and there was no clear difference in proportion of this group between the epi- and mesopelagic samples. In the microplankton fraction, the diatoms dominated, with 30 %–73 % of the reads. Dinophyceae was the second most abundant group in this fraction, with 3 %–46 % of the reads. In the net haul samples, Dinophyceae and diatoms were the most abundant in the large nanoplankton and microplankton fraction, with 64 %–77 % and 12 %–20 % of the reads, respectively. In the microplankton fraction Radiolaria were also abundant, representing 7 %–30 % of the reads. ASV richness was slightly higher than in May in the large nanoplankton and microplankton fraction. Syndiniales and Dinophyceae also had the highest richness in these fractions, followed by diatoms and ciliates.
In November, the proportion of reads assigned to phototrophs was less than 3 % in most samples in the pico- and nanoplankton. In the large nanoplankton and microplankton fraction, diatom reads constituted 1 %–33 %. In the picoplankton fraction, Syndiniales and Picozoa were the most abundant, with 40 %–75 % and up to 25 % of the reads, respectively. Radiolaria represented 44 % of the reads in the sample N04_1000. Dinophyceae was the most abundant group in the fractions between 3 and 50 µm, with 28 %–76 % of the reads. In the microplankton fraction, Radiolaria, Dinophyceae, and Syndiniales were the most abundant with up to 77 %, 43 %, and 42 % of the reads, respectively. In the net hauls, Ciliophora was also abundant, with up to ca. 30 % of the reads in each size fraction. ASV richness was generally higher this month than in May and August, especially in the small and large nanoplankton fractions. Syndiniales and Dinophyceae also had the highest richness this month.
The fastq files with raw 18s rRNA V4 reads are available on the European Nucleotide Archive repository under project number PRJEB40133. The untransformed ASV table, metadata table, and a table with environmental data are deposited in the Sea scientific open data publication repository (SEANOE), under the CC-BY license, with DOI https://doi.org/10.17882/79823 (Egge et al., 2014). The ASV tables, including the ASV sequences and assigned taxonomy; R-scripts for producing the figures and tables; and a Shiny application with interactive versions of the figures and tables are deposited on GitHub: https://github.com/EEgge/micropolar_protists_datapaper (last access: 30 August 2021; https://doi.org/10.5281/zenodo.5517980, Egge and Vaulot, 2021a). The Shiny app can be found at https://micropolar-protists.metapr2.org/ (Egge and Vaulot, 2021b), or opened in RStudio by running the following command:
shiny::runGitHub("micropolar_protists_datapaper","EEgge", ref = "main").
This dataset offers novel insights into the spatial and seasonal diversity and taxonomic composition of the protist community in the Atlantic gateway to the Arctic Ocean. It is the first study to provide data on the eukaryote microbial community throughout a complete year and down to 1000 m in this area of the Arctic. It forms the basis for future studies to detect changes in the eukaryote microbial community and for more detailed studies on the dynamics and community structure of specific taxonomic groups.
The study was conceptualized by AL, GB, BE, DV, and UJ. Data were curated by EE, BE, and DV. Formal analyses were performed by EE, BE, and DV. Funding was acquired by AL, GB, BE, DV, and UJ. Investigation was performed by AL, GB, BE, UJ, SE, and EE. The project was administered by AL and GB. Visualization was performed by EE, DV, and BE. Writing of the original draft was done by EE, BE, and DV. Reviewing and editing were performed by EE, BE, DV, SE, AL, GB, and UJ.
The contact author has declared that neither they nor their co-authors have any competing interests.
Publisher's note: Copernicus Publications remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This article is part of the special issue “Extreme environment datasets for the three poles”. It is not associated with a conference.
We wish to thank members of the MicroPolar and Carbon Bridge projects for assisting in the sampling campaigns and the crews at K/V Svalbard (January cruise), R/V Lance (March), and R/V Helmer Hanssen (May, August, and November cruise).
The study was conducted as part of the Research Council of Norway project Micropolar – Processes and Players in Arctic Marine Pelagic Food Webs – Biogeochemistry, Environment and Climate Change no. 225956/E10. Daniel Vaulot was supported by ANR contract PhytoPol (ANR-15-CE02-0007).
This paper was edited by David Carlson and reviewed by two anonymous referees.
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