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Fig. 2 in Four newly recorded species of planktonic cyanobacteria (Oscillatoriales, Cyanobacteria) in Korea

Fig. 2. Microscopic photographs of Planktothricoides raciborskii FBCC-A1472. (A, B) Arrangement of filament in the colony, (C, D) Sur- face of trichomes, (E-J) Apical cell of trichomes. Scale bars (A) 50 μm, (B) 20 μm, (C-J) 10 μm.

Fig. 3 in Four newly recorded species of planktonic cyanobacteria (Oscillatoriales, Cyanobacteria) in Korea

Fig. 3. Microscopic photographs of Planktothrix spiroides SJH-1. (A, B) Arrangement of filament in the colony, (C-J) Apical cell of trichomes. Scale bars (A, B) 20 μm, (C-J) 10 μm.

Fig. 1 in Four newly recorded species of planktonic cyanobacteria (Oscillatoriales, Cyanobacteria) in Korea

Fig. 1. Microscopic photographs of Laspinema thermale FBCC-A1475. (A, B) Arrangement of filament in the colony, (C-H) Apical cell of trichomes, (E) Necridic cell. Scale bars (A, B) 20 μm, (C-H) 10 μm.

Fig. 5 in Four newly recorded species of planktonic cyanobacteria (Oscillatoriales, Cyanobacteria) in Korea

Fig. 5. Maximum-Likelihood (ML) phylogenetic tree based on 16S rRNA gene sequences of Laspinema thermale, Planktothricoides raciborskii, Planktothrix spiroides, Cephalothrix lacustris, and other cyanobacterial strains. A 16S rRNA gene sequences of Gloeobacter violaceus (Gloeobacteraceae), Pseudanabaena catenata (Pseudanabaenaceae) were included as the outgroups. The support values at the nodes are written as follows: ML/Bayesian. Support values are displayed at nodes for>50% ML bootstrap proportions and>0.5 Bayesian posterior probability. The branch lengths are proportional to the scale given. Bold represents data obtained in this study.

Fig. 5 in Five newly recorded species of cyanobacteria in Korea

Fig. 5. Microphotographs of Tildeniella torsiva from the strain FBCC-A1474. (A) Arrangement of filament in the colony, (B) Curved terminal cells, (C) Apical cell, (D, E) Sheaths (sh), (F, G) False branching, (H-J) Morphologies of trichomes, (K) Diversity of cells morphology. Scale bars = (A) 20 μm, (B-K) 10 μm.

Fig. 4 in Four newly recorded species of planktonic cyanobacteria (Oscillatoriales, Cyanobacteria) in Korea

Fig. 4. Microscopic photographs of Cephalothrix lacustris FBCC-A1473. (A, B) Arrangement of filament in the colony, (C-H) Apical cell of trichomes, (C, D, H, I, L) Aerotopes, (F-H, J-L) Apical cell strongly capitate with calyptra, (K) Necridic cell. Scale bars (A) 50 μm, (B) 20 μm, (C-L) 10 μm.

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Fig. 4 in Two newly recorded echinoderms from the mesophotic zone in Korea

Fig. 4. Distribution of Parastichopus nigripunctatus (Augustin, 1908) based on the present and previous study.

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Fig. 3. Henricia irregularis Hayashi, 1940 in Two newly recorded echinoderms from the mesophotic zone in Korea

Fig. 3. Henricia irregularis Hayashi, 1940 in this study. (A) abactinal paxillae; (B) abactinal skeleton; (C) papulae (arrows); (D) madreporite; (E) actinal skeleton; (F), (I) adambulacral spines; (G) oral part and interradii of actinal side; (H) abactinal spines. Scale bars: A-E = 1 mm, F = 5 mm, G = 3 mm, H = 100 μm, I = 200 μm (H, I, SEM images). Abbreviations: a, adambulacral plates; i, inferomarginal plates; in, intermarginal plates; s, superomarginal plates; v, ventrolateral plates.

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Fig. 6 in Two newly recorded echinoderms from the mesophotic zone in Korea

Fig. 6. Ossicles of Parastichopus nigripunctatus (Augustin, 1908) in this study. (A) perforated plates in dorsal body wall; (B) tables in dorsal body wall; (C) rods in tentacle.

Fig. 1 in Morphological description and molecular analysis of newly recorded Anneissia pinguis (Crinoidea: Comatulida: Comatulidae) from Korea

Fig. 1. Anneissia pinguis (AH Clark, 1909). (A) oral view; (B) aboral view; (C) centrodorsal; (D) oral surface and distal pinnules; (E) aboral side; (F) cirrus. AP, anal papilla; C, centrodorsal; CS, cirrus socket; CR, cirrus; M, mouth; PC, pinnule comb; PD, distal pinnule. Scale bars = 10 mm.

Fig. 2 in Morphological description and molecular analysis of newly recorded Anneissia pinguis (Crinoidea: Comatulida: Comatulidae) from Korea

Fig. 2. Neighbor-joining tree of the aligned 596 bp COI sequence for 12 species of tribe Comasterini based on the Kimura 2-parameter model. The GenBank accession numbers used are indicate on each node. Bootstrap values were supported at ≥70.

Fig. 5 in Newly recorded chlorophytes, Monoraphidium subclavatum, Deuterostichococcus epilithicus, and Pseudostichococcus monallantoides in Korea

Fig. 5. Phylogenetic relationships of chlorophyte species within the family Stichococcaceae inferred from nearly complete 18S rDNA sequences with the maximum-likelihood (ML) algorithm. 18S sequences of genera (Bracteacoccus cohaerens, Accession No. HQ246325/ Pediastrum duplex, Accession No. AY780662) were included as the outgroup. Additionally, the probability of NJ analysis was incorporated into the ML tree to support the strength of each branch. The first and second numbers at the nodes display the bootstrap proportions (BP) (>50%) in ML and NJ, respectively. The branch lengths are proportional to the scale given.

Fig. 3 in Newly recorded chlorophytes, Monoraphidium subclavatum, Deuterostichococcus epilithicus, and Pseudostichococcus monallantoides in Korea

Fig. 3. Microscopic photographs of Pseudostichococcus monallantoides L.Moewus. NIBRCL0000114571. (A-D) long and cylindrical shapes, (E-H) mostly grows in a solitary state during culture. Scale bar represents 10 μm.

Fig. 2 in Newly recorded chlorophytes, Monoraphidium subclavatum, Deuterostichococcus epilithicus, and Pseudostichococcus monallantoides in Korea

Fig. 2. Microscopic photographs of Deuterostichococcus epilithicus Pröschold and Darienko. NIBRCL0000114567. (A-F) slightly curved cylindrical-shapes, (G, J) colony forming circle, (H, I) weakly connected filaments. Scale bar represents 10 μm.

Fig. 4 in Newly recorded chlorophytes, Monoraphidium subclavatum, Deuterostichococcus epilithicus, and Pseudostichococcus monallantoides in Korea

Fig. 4. Phylogenetic relationships of chlorophytes within the family Selenastraceae inferred from nearly complete 18S rDNA sequences with the maximum-likelihood (ML) algorithm. 18S sequences of genera (Bracteacoccus cohaerens, Accession No. HQ246325/ Pediastrum duplex, Accession No. AY780662) were included as the outgroup. Additionally, the probability of NJ analysis was incorporated into the ML tree to support the strength of each branch. The first and second numbers at the nodes display the bootstrap proportions (BP) (>50%) in ML and NJ, respectively. The branch lengths are proportional to the scale given.

Fig. 1 in Newly recorded chlorophytes, Monoraphidium subclavatum, Deuterostichococcus epilithicus, and Pseudostichococcus monallantoides in Korea

Fig. 1. Microscopic photographs of Monoraphidium subclavatum Nygaard FBCC-A409. (A, B) spindle-shapes, (C-H) slightly and moderate crescent-shapes, (I-L) autospores in the mother cell. Scale bar represents 10 μm.

Plate 1 in Five newly recorded foraminifera from off the southern coast of Jeju Island, Korea

Plate 1. Photomicrograph and SEM image of the newly recorded species. 1. Rhabdammina abyssorum Sars in Carpenter, 1869; side view. 2. (a-b) Ammolagena clavata (Jones & Parker, 1860); 2a. Side view; 2b. Side view SEM image; scales: 200 μm. 3. (a-b) Nodosaria lamnulifera Boomgaart, 1950; 3a. Side view; 3b. Side view SEM image. 4. Uvigerina schwageri Brady, 1884; 4a. Side view; 4b. Side view SEM image; scales: 200 μm. 5. (a-c) Neoeponides bradyi (Le Calvez, 1974); SEM image; 5a. Ventral side view; 5b. Spiral side view; 5c. Lateral side view; scales: 200 μm.

Fig. 18 in Brief description of 18 newly recorded ciliate species from soil and inland waters (Protozoa, Ciliophora) in South Korea

Fig. 18. Pseudovorticella vestita from life (A), after protargol impregnation (B, C). A. Body shape in vivo to show pellicular vesicles. B. Two kinds of macronuclear pattern (globular type and longitudinal J-shaped type). C. Infundibular polykineties 1-3. MA, macronuclear nodules; P1-3, infundibular polykineties. Scale bar = 30 μm.

Fig. 17 in Brief description of 18 newly recorded ciliate species from soil and inland waters (Protozoa, Ciliophora) in South Korea

Fig. 17. Epistylis pygmaeum from life (A-C) and after protargol impregnation (D, E). A. Epibiotic habitat of E. pygmaeum. B. Body shape and contractile vacuole in vivo. C. Dichotomously branched stalk. D. Infundibular polykinety 1-3. E. Macronucleus and silverline systems. Scale bars = 200 μm (A); 50 μm (B); 20 μm (D); 10 μm (E).

Fig. 15. Bryometopus triquetrus after protargol impregnation. A in Brief description of 18 newly recorded ciliate species from soil and inland waters (Protozoa, Ciliophora) in South Korea

Fig. 15. Bryometopus triquetrus after protargol impregnation. A. Somatic ciliature and contractile vacuole pore (arrow). B. Triangular oral cavity. C. Single macronucleus. LF, left oral ciliary field; MA, macronucleus; RF, right oral ciliary field. Scale bars = 20 μm.