Ulleungdo and Dokdo, located to the east of the Korean peninsula, are volcanic islands formed by the lava flows resulting from volcanic activity. Ulleungdo consists of one main island, with Seonginbong as its highest peak, and several small islets. Dokdo comprises two major islets, Dongdo and Seodo, and several exposed rocks (Sohn 1995; Kim et al. 2013). Ulleungdo and Dokdo share an oceanic climate due to the influence of warm and cold currents (Chang et al. 2002; Lee et al. 2010), although average annual precipitation is higher on Ulleungdo (1574 mm) than on Dokdo (660 mm). Annual average temperatures of both islands range from 12°C to 14°C (Chang et al. 2002; Lee et al. 2010). These islands are characterized by steep slopes that facilitate significant surface runoff when it rains, and it is thereby difficult for rainwater to collect on the surface. Indeed, volcanic islands formed from the lava are often characterized by a water-deficient environment. However, Ulleungdo and Dokdo have springs or small streams that originate from the groundwater to create an environment wherein fresh surface water is available (Sohn 1995; Chang et al. 2002).
The uneven distribution of freshwater sources influences the overall vegetation community and its successional processes. Ulleungdo, due to its relatively high precipitation, has greater vegetation species richness, with 487 vascular plants species and 104 woody plant species, than Dokdo, with 46 vascular plant species and eight woody plant species (Shin et al. 2004; Kim et al. 2007; Park et al. 2010), indicating that Ulleungdo is at a more advanced successional stage than Dokdo (Kim et al. 2007; Park et al. 2010; Jung et al. 2014). These patterns also extend to the microbial ecosystems, meaning that the different environments of Ulleungdo and Dokdo affect their microbial communities (Busse et al. 2006; Han et al. 2007; Djukic et al. 2010; Merilä et al. 2010). However, previous studies on the microbial communities on these islands have focused on the fungal and bacterial complements thereof (Kim et al. 2014; Nam et al. 2015), and little is known about the microalgal constituent. The discovery of new microalgal species is important in terms of the use of the algal biomass as a biological resource under different environmental conditions (Krustok et al. 2015).
Microalgae participate in carbon, nitrogen, and phosphorus cycles (Lehman 1980; Berner 1992; Vitousek et al. 2002) and, as photosynthetic organisms, are key producers and pioneers across a range of ecosystems (Booth 1941; Jackson 1971; Bellinzoni et al. 2003). In early successional stages, microalgae are the predominant production group, facilitating the subsequent arrival of herbaceous and woody plants, which can grow in the fertilized environment created by the micro algae (Booth 1941; Jackson 1971; Bellinzoni et al. 2003). The microalgal group promotes successional vegetation processes and allows for the emergence of predators and pathogenic microbes. The former mainly comprises zooplankton such as nematodes and arthropods (Havens and DeCosta 1987; Canovas et al. 1996; Mayer et al. 1997), while the latter causes disease in plants and animals and inhibits the biodegradation capacity of microbes (Littler and Littler 1998; Chen et al. 2014).
Interactions between microalgae and their abiotic and biotic environments drive the evolution of the microalgal community. Species dominance depends on environmental conditions, such as inorganic nutrient composition, water temperature, and light (Prowse and Talltng 1958; Goldman and Shapiro 1973; Porter 1977). In particular, microalgae composition is dominated by large-cell and needle-type algae, which are difficult to prey. Because the microalgal community supports the ecosystem and serves the producer-consumer relationship, analysis of this community can improve our understanding of the local environment, elemental recycling (carbon, nitrogen, and phosphorus), and micro-ecosystem relationships between producer and consumer trophic levels (Berner 1992; Vitousek et al. 2002; Cardinale et al. 2011). However, microalgal community research based solely on the culturing faces certain limitations, particularly the difficulty in identifying and analyzing unculturable microorganisms (Handelsman 2004; Streit and Schmitz 2004). Consequently, amplicon sequencing analysis using Illumina MiSeq can be a powerful tool for the investigation of unculturable microorganisms in their natural environment (Knight 2000; Handelsman 2004; Streit and Schmitz 2004; Schloss and Handelsman 2005).
Previous studies have yet to analyze the microalgal communities in the freshwater ecosystems on Ulleungdo (Seonginbong) and Dokdo (Dongdo and Seodo). This study investigated eukaryotic microalgal communities on these islands by taking freshwater samples from groundwater and tributary streams for the Illumina MiSeq analysis. Illumina MiSeq allows a large amount of sequencing information to be processed in a short time, and taxonomic analyses can then be conducted based on this information (Handelsman 2004; Streit and Schmitz 2004; Buée et al. 2009; Shokralla et al. 2012). In this study, microalgal species richness and diversity were characterized using taxonomic analysis, revealing that the composition of these communities varied by region, from phylum to species units.
Illumina MiSeq results for the operational taxonomic units (OTUs) and statistical analysis.
Seonginbong | Dongdo | Seodo | |
---|---|---|---|
Total reads | 580 853 | 534 141 | 469 920 |
Validated reads | 290 919 | 289 610 | 275 387 |
Mean read length (bp) | 408.1 | 416.7 | 412.54 |
Maximum read length (bp) | 418 | 418 | 408 |
Number of OTUs1 | 834 | 203 | 182 |
Chao12 | 834 | 203.75 | 182 |
Shannon3 | 6.722 | 2.038 | 5.118 |
Simpson4 | 0.9655 | 0.5569 | 0.9174 |
Goods Coverage5 | 1 | 0.9999 | 1 |
OTUs: Operational taxonomic units
Chao1: Species richness estimation
Shannon: Shannon diversity index (> 0, higher is more diverse)
Simpson: Simpson diversity index (0–1, 1 = most simple)
Goods Coverage: 1 – (number of singleton OTUs/number of sequences); 1 = 100% coverage
The species richness of the samples is represented by rarefaction curves in Fig. 1, while the Chao1 species richness, the Shannon diversity index, and the Simpson diversity index are summarized in Table I (Heck et al. 1975; Schloss et al. 2009). The Seonginbong sample had the greatest species richness for all indicators (Chao1: 934; Shannon: 6.7222; Simpson: 0.9655), while Dongdo and Seodo had similar results to one another for Chao1 (203.75 and 182, respectively). However, Seodo had Shannon and Simpson index scores (5.118 and 0.9174, respectively) that were similar to those at Seonginbong (6.722 and 0.9655, respectively), and much higher than those of Dongdo (2.038 and 0.5569, respectively). Based on the OTU and species richness results, the diversity of the eukaryotic microbial composition on Seonginbong appeared to be greater than on Dongdo and Seodo (Fig. 1 and Table I). These results confirmed differences in species diversity among Seonginbong, Dongdo, and Seodo.
Number of eukaryotic microalgal taxa observed in the Seonginbong, Dongdo, and Seodo samples.
Seonginbong | Dongdo | Seodo | ||||
---|---|---|---|---|---|---|
c1 | uc2 | c1 | uc2 | c1 | uc2 | |
Phylum | 165 646 | 125 273 | 30 911 | 258 699 | 164 678 | 110 709 |
Class | 128 160 | 162 759 | 23 011 | 266 599 | 144 662 | 130 725 |
Order | 99 964 | 190 955 | 22 791 | 266 819 | 123 329 | 152 058 |
Family | 96 751 | 194 168 | 22 751 | 266 859 | 120 206 | 155 181 |
Genus | 92 628 | 198 291 | 22 707 | 266 903 | 110 674 | 164 713 |
Species | 84 154 | 206 765 | 17 930 | 271 680 | 97 541 | 177 846 |
Number of sequencing reads with a scientific name for the taxon (classified,
Number of sequencing reads either unclassified into a sublevel or classified as an unknown name for the taxon (unclassified,
The taxonomic compositions of the eukaryotic microbial communities on Seonginbong, Dongdo, and Seodo were then analyzed. It was found that the communities contained a combination of 17 phyla: Xanthophyceae, Streptophyta, Rotifera, Porifera, Platyhelminthes, Nematoda, Eustigmatophyceae, Chytridiomycota, Chordata, Chlorophyta, Blastocladiomycota, Basidiomycota, Bacillariophyta, Ascomycota, Arthropoda, Apicomplexa, and Annelida (Fig. 2). The communities were dominated by the microalgal phyla Chlorophyta and Bacillariophyta, although their combined relative abundance was significantly higher in the Dongdo and Seodo samples (93.52% and 91.77%, respectively) than in the Seonginbong sample (31.02%). Differences in population densities were more profound in the Seonginbong sample than in the Dongdo and Seodo samples (Fig. 2). This analysis of differences in the community composition could contribute significantly to our understanding of the microbial ecosystems at each site (Wegley et al. 2007; Rodriguez-Brito et al. 2010; Fierer et al. 2012). Microbial community compositions already reported suggest a need for further research on the eukaryotic microorganisms in each region (Knight 2000; Chiao 2004; Schloss and Handelsman 2005). In this regard, amplicon sequencing using Illumina MiSeq is a powerful tool for the identification of unculturable microalgae. More important, MiSeq system analysis can also generate useful information on new species in the natural environments of Ulleungdo and Dokdo that could be helpful in studying unculturable eukaryotic microorganisms.
At the class level, five distinct microalgal classes (Bacillariophyceae, Coscinodiscophyceae, Chlorophyceae, Trebouxiophyceae, and Ulvophyceae) were detected in the overall sample (Fig. 3), with the dominant groups in each region differing: Seonginbong, Chlorophyceae; Dongdo, Trebouxiophyceae; and Seodo, Bacillariophyceae. In particular, the relative abundance of Bacillariophyceae was higher in Seodo (88.24%) than in Seonginbong (10.56%) or Dongdo (0%). The Coscinodiscophyceae was only present on Seodo (8.86%). In addition, two or three green algae classes were present at the study sites, including Chlorophyceae (73.39%), Trebouxiophyceae (11.17%), and Ulvophyceae (4.18%) on Seonginbong; Chlorophyceae (22.22%) and Trebouxiophyceae (77.67%) on Dongdo; and Chlo rophyceae (2.28%), Trebouxiophyceae (0.49%), and Ulvophyceae (0.13%) on Seodo.
A total of 30 families were detected in each region. Seventeen families had identified scientific names, and nine had a relative abundance of at least 1%. These families are summarized in Table III. On Seonginbong, three diatom families (
Relative abundance of eukaryotic microalgal families in the Seonginbong, Dongdo, and Seodo samples.
Taxonomy | Seonginbong | Dongdo | Seodo | ||||||
---|---|---|---|---|---|---|---|---|---|
Phylum | Class | Order | Family | %1 | Fr2 | %1 | Fr2 | %1 | Fr2 |
Bacillariophyta | Bacillariophyceae | – | – | 0.00 | 0 | 0.00 | 0 | 21.62 | 59 531 |
Bacillariophyta | Bacillariophyceae | – | Achnanthaceae | 0.00 | 0 | 0.00 | 0 | 1.54 | 4 239 |
Bacillariophyta | Bacillariophyceae | – | Bacillariaceae | 0.15 | 423 | 0.00 | 0 | 3.26 | 8 974 |
Bacillariophyta | Bacillariophyceae | Naviculales | Amphipleuraceae | 0.00 | 0 | 0.00 | 0 | 0.23 | 645 |
Bacillariophyta | Bacillariophyceae | Naviculales | Diadesmidaceae | 0.00 | 0 | 0.00 | 7 | 2.38 | 6 551 |
Bacillariophyta | Bacillariophyceae | Naviculales | Naviculaceae | 0.00 | 0 | 0.00 | 0 | 0.29 | 802 |
Bacillariophyta | Bacillariophyceae | Naviculales | Pinnulariaceae | 0.09 | 256 | 0.00 | 0 | 0.00 | 0 |
Bacillariophyta | Bacillariophyceae | Naviculales | Sellaphoraceae | 0.00 | 0 | 0.00 | 0 | 3.12 | 8 579 |
Bacillariophyta | Bacillariophyceae | Naviculales | Stauroneidaceae | 1.16 | 3 379 | 0.00 | 0 | 0.00 | 0 |
Bacillariophyta | Bacillariophyceae | Thalassiophysales | Catenulaceae | 0.00 | 0 | 0.00 | 0 | 0.12 | 329 |
Bacillariophyta | Coscinodiscophyceae | Melosirales | Stephanopyxidaceae | 0.00 | 0 | 0.00 | 0 | 3.14 | 8 660 |
Bacillariophyta | Coscinodiscophyceae | Paraliales | – | 0.00 | 0 | 0.00 | 0 | 0.13 | 354 |
Chlorophyta | – | – | – | 0.00 | 0 | 0.02 | 65 | 0.00 | 0 |
Chlorophyta | – | Chlorodendrales | – | 0.00 | 0 | 0.01 | 21 | 0.00 | 0 |
Chlorophyta | Chlorophyceae | – | – | 0.03 | 91 | 0.00 | 13 | 0.62 | 1 708 |
Chlorophyta | Chlorophyceae | Chlamydomonadales | – | 2.53 | 7 368 | 0.09 | 271 | 0.00 | 0 |
Chlorophyta | Chlorophyceae | Chlamydomonadales | Characiochloridaceae | 0.34 | 1 002 | 0.00 | 0 | 0.00 | 0 |
Chlorophyta | Chlorophyceae | Chlamydomonadales | Chlamydomonadaceae | 0.38 | 1 096 | 0.02 | 48 | 0.00 | 0 |
Chlorophyta | Chlorophyceae | Chlamydomonadales | Chlorococcaceae | 1.53 | 4 437 | 18.46 | 53 463 | 0.00 | 0 |
Chlorophyta | Chlorophyceae | Chlorosarcinales | – | 1.29 | 3 761 | 0.00 | 0 | 0.00 | 0 |
Chlorophyta | Chlorophyceae | Sphaeropleales | – | 3.47 | 10 096 | 0.00 | 2 | 0.00 | 0 |
Chlorophyta | Chlorophyceae | Sphaeropleales | Scenedesmaceae | 0.08 | 243 | 0.00 | 0 | 0.22 | 597 |
Chlorophyta | Trebouxiophyceae | – | – | 0.56 | 1 624 | 0.00 | 0 | 0.12 | 329 |
Chlorophyta | Trebouxiophyceae | – | Coccomyxaceae | 0.01 | 23 | 0.00 | 0 | 0.00 | 0 |
Chlorophyta | Trebouxiophyceae | Chlorellales | – | 0.00 | 0 | 0.00 | 7 | 0.00 | 0 |
Chlorophyta | Trebouxiophyceae | Chlorellales | Chlorellaceae | 0.58 | 1 689 | 64.91 | 187 999 | 0.06 | 162 |
Chlorophyta | Trebouxiophyceae | Ctenocladales | Ctenocladaceae | 0.21 | 604 | 0.00 | 0 | 0.00 | 0 |
Chlorophyta | Trebouxiophyceae | Microthamniales | – | 0.11 | 323 | 0.02 | 48 | 0.00 | 0 |
Chlorophyta | Ulvophyceae | Ulotrichales | – | 0.55 | 1 605 | 0.00 | 0 | 0.00 | 0 |
Chlorophyta | Ulvophyceae | Ulvales | – | 0.00 | 0 | 0.00 | 0 | 0.05 | 136 |
The microalgal families detected in at least one of the three samples are shown. Unclassified taxonomic names (phylum, class, order, and family) are replaced with a dash (–)
Relative abundance
Frequency of microalgae detected at each sampling site
A total of 50 microalgal genera were detected, with 37 identified by scientific name. Fourteen genera had a relative abundance of at least 1% (Table ???). Three diatom genera (
For species-level analyses, the microalgal species identified from the Seonginbong, Dongdo, and Seodo samples were organized in a phylogenetic tree (Fig. 4). For groups without a scientific name at the genus level (Fig. 3), names were only added to those with scientific names at the species level (Fig. 4). Phylum and class boundaries were identified for the microalgal species based on species-level sequencing analysis for Seonginbong, Dongdo, and Seodo. In Fig. 4, the boundary between Bacillariophyta and Chlorophyta is marked with a yellow box, and boundaries between the classes belonging to each phylum are marked with purple boxes (Metting 1996). Among the microalgal groups, some of the Chlorophyceae belonged to Trebouxiophyceae from class via phylum (Tables III and IV). At the species level, dominant species were identified on each island, to include six species on Seonginbong, two species on Dongdo, and six species on Seodo; these are marked by boxes in Fig. 4 (Seonginbong, red; Dongdo, blue; Seodo, green). Of the species shown on the phylogenetic tree, some have been associated with shellfish toxins (Falconer 2012) frequently found on Seodo. In particular,
Relative abundance of eukaryotic microalgal genera in the Seonginbong, Dongdo, and Seodo samples.
Taxonomy | Seonginbong | Dor | gdo | Seodo | ||||||
---|---|---|---|---|---|---|---|---|---|---|
Phylum | Class | Order | Family | Genus | Fr2 | Fr2 | Fr2 | |||
Bacillariophyta | Bacillariophyceae | – | – | – | 0.00 | 0 | 0.00 | 0 | 0.86 | 2 363 |
Bacillariophyta | Bacillariophyceae | – | – | 0.00 | 0 | 0.00 | 0 | 20.76 | 57 168 | |
Bacillariophyta | Bacillariophyceae | – | Achnanthaceae | 0.00 | 0 | 0.00 | 0 | 1.54 | 4 239 | |
Bacillariophyta | Bacillariophyceae | – | Bacillariaceae | 0.15 | 423 | 0.00 | 0 | 0.00 | 0 | |
Bacillariophyta | Bacillariophyceae | – | Bacillariaceae | 0.00 | 0 | 0.00 | 0 | 3.26 | 8 974 | |
Bacillariophyta | Bacillariophyceae | Naviculales | Amphipleuraceae | 0.00 | 0 | 0.00 | 0 | 0.23 | 645 | |
Bacillariophyta | Bacillariophyceae | Naviculales | Diadesmidaceae | 0.00 | 0 | 0.00 | 0 | 2.15 | 5 922 | |
Bacillariophyta | Bacillariophyceae | Naviculales | Diadesmidaceae | 0.00 | 0 | 0.00 | 7 | 0.23 | 629 | |
Bacillariophyta | Bacillariophyceae | Naviculales | Naviculaceae | 0.00 | 0 | 0.00 | 0 | 0.29 | 802 | |
Bacillariophyta | Bacillariophyceae | Naviculales | Pinnulariaceae | 0.09 | 256 | 0.00 | 0 | 0.00 | 0 | |
Bacillariophyta | Bacillariophyceae | Naviculales | Sellaphoraceae | 0.00 | 0 | 0.00 | 0 | 3.12 | 8 579 | |
Bacillariophyta | Bacillariophyceae | Naviculales | Stauroneidaceae | 1.16 | 3 379 | 0.00 | 0 | 0.00 | 0 | |
Bacillariophyta | Bacillariophyceae | Thalassiophysales | Catenulaceae | 0.00 | 0 | 0.00 | 0 | 0.12 | 329 | |
Bacillariophyta | Coscinodiscophyceae | Melosirales | Stephanopyxidaceae | 0.00 | 0 | 0.00 | 0 | 3.14 | 8 660 | |
Bacillariophyta | Coscinodiscophyceae | Paraliales | – | 0.00 | 0 | 0.00 | 0 | 0.13 | 354 | |
Chlorophyta | – | – | – | 0.00 | 0 | 0.02 | 65 | 0.00 | 0 | |
Chlorophyta | – | Chlorodendrales | – | 0.00 | 0 | 0.01 | 21 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | – | – | 0.03 | 91 | 0.00 | 13 | 0.62 | 1708 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | – | 1.48 | 4 308 | 0.09 | 249 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | – | 0.00 | 0 | 0.01 | 22 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | – | 0.62 | 1 793 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | – | 0.44 | 1 267 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | Characiochloridaceae | 0.34 | 1002 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | Chlamydomonadaceae | 0.02 | 50 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | Chlamydomonadaceae | 0.35 | 1026 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | Chlamydomonadaceae | 0.01 | 20 | 0.02 | 48 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlamydomonadales | Chlorococcaceae | 1.53 | 4 437 | 18.46 | 53 463 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Chlorosarcinales | – | 1.29 | 3 761 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Sphaeropleales | – | 1.47 | 4 271 | 0.00 | 2 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Sphaeropleales | – | 1.89 | 5 490 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Sphaeropleales | – | 0.12 | 335 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Chlorophyceae | Sphaeropleales | Scenedesmaceae | 0.02 | 64 | 0.00 | 0 | 0.22 | 597 | |
Chlorophyta | Chlorophyceae | Sphaeropleales | Scenedesmaceae | 0.06 | 179 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | – | – | 0.04 | 102 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | – | – | 0.51 | 1487 | 0.00 | 0 | 0.12 | 329 | |
Chlorophyta | Treb ouxiophyceae | – | – | 0.01 | 35 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | – | Coccomyxaceae | 0.01 | 23 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Chlorellales | – | 0.00 | 0 | 0.00 | 7 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Chlorellales | Chlorellaceae | 0.06 | 182 | 63.78 | 184 700 | 0.06 | 162 | |
Chlorophyta | Treb ouxiophyceae | Chlorellales | Chlorellaceae | 0.34 | 999 | 0.00 | 2 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Chlorellales | Chlorellaceae | 0.04 | 102 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Chlorellales | Chlorellaceae | 0.00 | 0 | 0.00 | 12 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Chlorellales | Chlorellaceae | 0.00 | 14 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Chlorellales | Chlorellaceae | 0.13 | 392 | 1.13 | 3 285 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Ctenocladales | Ctenocladaceae | 0.21 | 604 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Microthamniales | – | 0.09 | 272 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Microthamniales | – | 0.02 | 51 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Treb ouxiophyceae | Microthamniales | – | 0.00 | 0 | 0.02 | 48 | 0.00 | 0 | |
Chlorophyta | Ulvophyceae | Ulotrichales | – | 0.55 | 1605 | 0.00 | 0 | 0.00 | 0 | |
Chlorophyta | Ulvophyceae | Ulvales | – | 0.00 | 0 | 0.00 | 0 | 0.05 | 136 |
The microalgal genera detected in at least one of the three samples are shown. Unclassified taxonomic names (phylum, class, order, family, and genus) are replaced with a dash (–)
Relative abundance
Frequency of microalgae detected at each sampling site
We organized the three microalgal communities from the phylum to species levels to analyze the taxono mic compositions of the three study sites. The approximate amount of available sunlight was highest at the Seonginbong sampling site and lowest at the Seodo site (Supplementary Fig. S1), and the relative abundance of diatoms strongly correlated with sunlight availability (Hudon and Bourget 1983; Post et al. 1984; Lange et al. 2011). Our results and those from previous studies indicate that further research on the relationship between light and microalgal community composition is required. Research also suggests that microalgal community composition is influenced by natural enemies or disease (Hudon and Bourget 1983; Post et al. 1984; Lange et al. 2011). In accordance with these findings, we observed differences in natural compositions among Seonginbong, Dongdo, and Seodo; the microalgal group was dominant on Seodo. At the phylum level, Seonginbong was characterized by zooplankton and pathogenic fungal groups (Fig. 2). At the class level, the microalgal group was dominated by Chlorophyceae on Seonginbong and Trebouxiophyceae (particularly
Previous studies also indicate that microalgae can affect the external environment. A previous report found that the
The present study analyzed the overall species richness and taxonomic compositions of the microalgal communities of Ulleungdo (Seonginbong) and Dokdo (Dongdo and Seodo). Amplicon sequencing analysis was performed using Illumina MiSeq, and microbiological OTUs from Seonginbong (834), Dongdo (203), and Seodo (182) were identified. Three indicators (Chao1, Shannon, and Simpson) were used to analyze species richness, and it was found that the species richness of Seonginbong was higher than those of Dongdo and Seodo. Classified reads were used for taxonomic analysis, with the communities exhibiting differences in their composition from the phylum to species levels. In the Seonginbong sample, several other eukaryotic microorganisms were present in the community in addition to microalgae, while microalgae (Chlorophyta) and diatoms (Bacillariophyta) were found to be extremely dominant on Dongdo and Seodo, respectively. Analyses of the relative abundances of the different communities added details to information regarding the differences in species richness between the three regions. We obtained information on microalgae on Seonginbong, Dongdo, and Seodo via MiSeq tools; however, MiSeq analysis does have some limitations with regards to dependence on existing taxonomies in screening and identifying microalgal species. Despite these experimental limitations, MiSeq analysis provided in-depth information on the microalgae communities of Ulleungdo and Dokdo.