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Fig. 10. Drawida koreana koreana Kobayashi, 1938 in Reports of Drawida (Oligochaeta: Moniligastridae) from far East Asia

Fig. 10. Drawida koreana koreana Kobayashi, 1938. After Kobayashi (1938: fig. 3) showing (a) male field, (b and c) enlarged spermathecae. Note that his sketch of the male field of D. koreana is similar to that found in several current specimens.

Fig. 9. Drawida moriokaensis Ohfuchi, 1938 in Reports of Drawida (Oligochaeta: Moniligastridae) from far East Asia

Fig. 9. Drawida moriokaensis Ohfuchi, 1938. After Ohfuchi (1938: 44, figs. 10-11) showing male field, gizzards and dorsal blood vessel, a spermatheca (Sp. spermathecal ampulla, Sp.Atr. spermathecal atrium) and male organs (T.s.‾Testis sac).

Fig. 8. Drawida tairaensis Ohfuchi, 1938 in Reports of Drawida (Oligochaeta: Moniligastridae) from far East Asia

Fig. 8. Drawida tairaensis Ohfuchi, 1938. After Ohfuchi (1938: figs. 6-9) showing spermathecal and male field of one specimen and male field of another with male pores retracted; gizzards and dorsal blood vessels from two different specimens with that on rhs also having ovisac plus upper sketches of two sets of spermathecae, that on rhs having accessory gland, and two sets of male organs (T.s. testis sacs and M. Atr male atria).

Fig. 7. Drawida ofunatoensis Ohfuchi, 1938 in Reports of Drawida (Oligochaeta: Moniligastridae) from far East Asia

Fig. 7. Drawida ofunatoensis Ohfuchi, 1938. After Ohfuchi (1938; figs. 1-5) showing spermathecal and male fields of two somewhat different specimens, internal organs and rhs enlargements of male terminalia (testis sac with vas deferend to prostate, and section of stubby penis in pouch), a nephridium and a spermatheca.

Fig. 5. A lhs. Drawida gisti gisti Michaelsen, 1931 in Reports of Drawida (Oligochaeta: Moniligastridae) from far East Asia

Fig. 5. A lhs. Drawida gisti gisti Michaelsen, 1931. After Kobayashi (1938: 85, fig. 2) of Korean mainland specimen showing (a) male field, (b) male terminalia and (c) distinctive spermatheca in 8. 5B rhs. Drawida angchiniana Chen, 1933. After Kobayashi (1937: fig. 1) of a Jeju Island specimen showing (A) male field, (B) spermatheca with atrium and associated gland in segement 7.

Fig. 6. Drawida nemora Kobayashi, 1936 in Reports of Drawida (Oligochaeta: Moniligastridae) from far East Asia

Fig. 6. Drawida nemora Kobayashi, 1936. After Kobayashi (1936: fig. 1). 1. Ventral view. 2. Male field with GMs. 3. Spermathecal pore in 7/8. 4. Internal organs. 5. Ventral view of prostate and penis with vas deferens. 6. Section of prostate and penis. 7. Spermatheca (Codes: bw. Body wall, giz. Gizzard, gp. Genital papilla, o. Ovary, och. Ovarian chamber, ovs. Ovisac, p. Penis, pr. Prostate, sp. Spermatheca, ts. Testis sac, vd. Vas deferens).

Fig. 1 in Reports of Drawida (Oligochaeta: Moniligastridae) from far East Asia

Fig. 1. Evolutionary relationships of taxa from MEGA6 defaults-generated phylogram after Clustal alignment (with WO22 sequence complements reversed) using the Minimum Evolution method optimal tree, drawn with branch lengths to scale (sum of units = 1.33) [see Tamura et al. (2013)]. Asterisked (*) at top lhs is independent analysis of sub-tree; at bottom lhs is Distance Scale bar. Sample codes and provisional or new species names are explained in the text and Appendix legend; closed red circles () are Japanese samples, solid yellow squares (¥) are from Jeju; black diamonds are Philippines samples. Eukerria saltensis is the outgroup.

Fig. 2 in Reports of Drawida (Oligochaeta: Moniligastridae) from far East Asia

Fig. 2. Drawida cf. barwelli (Beddard, 1886). Ventral view of sectioned specimen with spermathecae in 8 and male organs in 10 in situ. Section shows gizzards in 15-18. Boxed is Kobayashi's (1941: fig. 1) of Ponape D. barwelli a. ventrum, b. spermathecae with both ampullae conjoined and (on rhs only, not shown lhs) long duct lacking atrium and glands. These are doubtfully the same species since Kobayashi's (1941) specimen lacks spermathecal atria.

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COMMENTS.— Although not breeding in the Mediterranean, the species forages in Libyan waters (van Dijk et al. 2014). In addition to the single beached record, an individual was pulled from nearshore waters of the Tajura coast in 1996 and died in the rehabilitation facility of the Marine Biology Research Centre (MBRC) at Tajura, where it was subsequently taxidermied at the MBRC Museum (Hamza 2010). Capra's (1949) records were based on a report in "L'Idea Coloniale" for 2 May 1927 (Mongàr) and an unspecified specimen in the Museo Civico di Storia Naturale di Trieste (Sella). IUCN THREAT STATUS.— Vulnerable A2bd. MAP 3. Distribution of Dermochelys coriacea in Libya showing stranding site records. in Atlas of the Reptiles of Libya

COMMENTS.— Although not breeding in the Mediterranean, the species forages in Libyan waters (van Dijk et al. 2014). In addition to the single beached record, an individual was pulled from nearshore waters of the Tajura coast in 1996 and died in the rehabilitation facility of the Marine Biology Research Centre (MBRC) at Tajura, where it was subsequently taxidermied at the MBRC Museum (Hamza 2010). Capra's (1949) records were based on a report in "L'Idea Coloniale" for 2 May 1927 (Mongàr) and an unspecified specimen in the Museo Civico di Storia Naturale di Trieste (Sella). IUCN THREAT STATUS.— Vulnerable A2bd. MAP 3. Distribution of Dermochelys coriacea in Libya showing stranding site records.

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Figure 3. – A in Figure 3 in First report of the Ecuadorian deep-sea scorpionfish, Trachyscorpia verai Béarez & Motomura, 2009 (Actinopteri: Scorpaenidae) from Peruvian marine waters

Figure 3. – A: Pisang River, Padang City, West Sumatra Province, Indonesia (1°07'05"S, 100°23'56"E) (photograph by Ari Wright). B: Way Lalaan River, Tenggamus Regency, Lampung Province, Indonesia (5°29'12"S, 104°41'29"E) (photograph by Ari Wright).

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Figure 2 in Figure 3 in First report of the Ecuadorian deep-sea scorpionfish, Trachyscorpia verai Béarez & Motomura, 2009 (Actinopteri: Scorpaenidae) from Peruvian marine waters

Figure 2. – Distribution map of Belobranchus segura. First records in Sumatra, Indonesia (black stars, this study) and previous published records (black triangles) based on Keith et al. (2012, 2021), Kottelat (2013), Miesen et al. (2016), Dahruddin et al. (2016) and Larson (2021).

Fig. 4 in A report of 46 unrecorded bacterial species in Korea belonging to the classes Alphaproteobacteria, Betaproteobacteria, Deltaproteobacteria and Epsilonproteobacteria

Fig. 4. Neighbor-joining phylogenetic tree, based on 16S rRNA sequences, showing the phylogenetic relationship between strains isolated in this study and their relatives in the orders Burkholderiales, Neisseriales, and Rhodocyclales in the class Betaproteobacteria. Parvularcula oceanus JLT2013T (JPHU01000026) was used as an outgroup. Bootstrap values (>70%) are shown above nodes. Scale bar: 0.02 changes per nucleotide.

Fig. 3 in A report of 46 unrecorded bacterial species in Korea belonging to the classes Alphaproteobacteria, Betaproteobacteria, Deltaproteobacteria and Epsilonproteobacteria

Fig. 3. Neighbor-joining phylogenetic tree, based on 16S rRNA sequences, showing the phylogenetic relationship between strains isolated in this study and their relatives in the orders Rhodobacterales, Rhodospirillales, and Sphingomonadales in the class Alphaproteobacteria. Burkholderia dabaoshanensis GIMN1.004T (FJ210816) was used as an outgroup. Bootstrap values (>70%) are shown above nodes. Scale bar: 0.02 changes per nucleotide.

Fig. 1 in A report of 46 unrecorded bacterial species in Korea belonging to the classes Alphaproteobacteria, Betaproteobacteria, Deltaproteobacteria and Epsilonproteobacteria

Fig. 1. Transmission electron micrographs or scanning electron micrographs of cells of the strains isolated in this study. The cells were cultured at their optimal growth conditions. Strains: 1, LPB0183; 2, LPB0211; 3, 17J44-22; 4, 17J27-16; 5, KYW1385; 6, BMW10; 7, IMCC34164; 8, IMCC34184; 9, IMCC34185; 10, IMCC34207; 11, IMCC34233; 12, GH4-12; 13, GH1-7; 14, GH1-10; 15, GH2-6; 16, Ibu_S_3; 17, MMS17- GJ036; 18, MMS17-SY214; 19, Gsoil 1028; 20, Gsoil 1111; 21, Gsoil318-1; 22, Gsoil 824; 23, HMF7612; 24, HMF7644; 25, HMF7868; 26, HMF8042; 27, HMF8046; 28, HMF8205; 29, HMF8467; 30, HMF8483; 31, HMF8486; 32, S-1; 33, F-mm3; 34, StC2; 35, BR3409; 36, JMn9; 37, WD42; 38, kw_8; 39, MMS17-GJ039; 40, Gsoil 096; 41, HMF7346; 42, HMF7693; 43, HMF7887; 44, HMF4721; 45, LPB0172; 46, LPB0305.

Fig. 2 in A report of 46 unrecorded bacterial species in Korea belonging to the classes Alphaproteobacteria, Betaproteobacteria, Deltaproteobacteria and Epsilonproteobacteria

Fig. 2. Neighbor-joining phylogenetic tree, based on 16S rRNA sequences, showing the phylogenetic relationship between strains isolated in this study and their relatives in the orders Parvularculales and Rhizobiales in the class Alphaproteobacteria. Burkholderia dabaoshanensis GIMN1.004T (FJ210816) was used as an outgroup. Bootstrap values (>70%) are shown above nodes. Scale bar: 0.02 changes per nucleotide.

Fig. 1 in A report of nine unrecorded bacterial species in the phylum Bacteroidetes collected from freshwater environments in Korea

Fig. 1. Transmission electron micrographs of the strains isolated in this study. Strains: A, SJ-153; B, SS1-37; C, BK-550; D, KS1-10; E, SJ- 361; F, ES1-03; G, BK-168; H, 04KS1-21; I, SJ-175. Bar: 0.2 μm (A-G), 0.5 μm (H and I).

Fig. 2 in A report of nine unrecorded bacterial species in the phylum Bacteroidetes collected from freshwater environments in Korea

Fig. 2. Neighbor-joining phylogenetic tree, based on 16S rRNA gene sequences, showing the relationships among the isolates and related taxa in the order Flavobacteriales. The values above each branch indicate the percentage levels of bootstrap support based on 1,000 resamplings (NJ/MP/ML). The closed circles indicate that the corresponding nodes were recovered by all treeing algorithms (NJ, MP and ML). Bar, 0.02 changes per nucleotide position.

Fig. 15 in A report of 14 unrecorded bacterial species in Korea isolated in 2017

Fig. 15. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences shows the relationship between the strains isolated in this study and their relatives of the genus Bacillus. Bootstrap values (>70%) are shown above nodes for the neighbor-joining methods. Bar: 0.0050 substitutions per nucleotide position, respectively.

Fig. 13 in A report of 14 unrecorded bacterial species in Korea isolated in 2017

Fig. 13. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences shows the relationship between the strains isolated in this study and their relatives of the genus Kurthia. Bootstrap values (>70%) are shown above nodes for the neighbor-joining methods. Bar: 0.0050 substitutions per nucleotide position, respectively.

Fig. 11 in A report of 14 unrecorded bacterial species in Korea isolated in 2017

Fig. 11. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences shows the relationship between the strains isolated in this study and their relatives of the genus Domibacillus. Bootstrap values (>70%) are shown above nodes for the neighbor-joining methods. Bar: 0.0050 substitutions per nucleotide position, respectively.