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Fig. 2 in Report on 30 unrecorded bacterial species of the phylum Firmicutes isolated from Korea in 2016

Fig. 2. Maximum-likelihood phylogenetic tree of isolates and related taxa belonging to the order Bacillales. Filled circles indicate the nodes that were recovered in the trees generated by both the neighbour-joining (NJ) and the maximum-likelihood (ML) methods. Numbers at nodes represent bootstrap values (NJ/ML) based on 1000 replicated datasets. Only values above 50% are shown. Bar, 0.1 substitutions per nucleotide position.

Fig. 1 in Report on 30 unrecorded bacterial species of the phylum Firmicutes isolated from Korea in 2016

Fig. 1. Transmission election micrographic and scanning electron micrographic images of isolated cells. Strains: 1, HMF7750; 2, ATS3402; 3, PTS2210; 4, AR23209; 5, PR23219; 6, PR23304; 7, AR23203; 8, PMA3404; 9, AMR3201; 10, AMR3203; 11, PR22215; 12, AR23201; 13, AMA2302; 14, ATS2307; 15, PR22212; 16, AR23202; 17, H18Y; 18, CAU 1342; 19, CAU 1339; 20, LPB0128; 21, LPB0129; 22, LPB0134; 23, LPB0160; 24, CF2; 25, NF3-3-1; 26, BE2-15; 27, BE2-30; 28, BE3-11; 29, JMW-27; 30, DMHB11.

Fig. 4 in A report of 42 unrecorded actinobacterial species in Korea

Fig. 4. Neighbor-joining phylogenetic tree, based on 16S rRNA gene sequences, showing the relationships between the strains isolated in this study and their relatives of the orders Micromonosporales, Propionibacteriales, Streptomycetales and Streptosporangiales in the class Actinobacteria. Asterisks indicate that the corresponding branches were also recovered in both the maximum-likelihood and maximum-parsimony trees. Bootstrap values (>60%) are shown at the branching points. Bar, 0.01 substitutions per nucleotide position.

Fig. 3 in Report on 30 unrecorded bacterial species of the phylum Firmicutes isolated from Korea in 2016

Fig. 3. Maximum-likelihood phylogenetic tree of isolates and related taxa belonging to the order Lactobacillales. Filled circles indicate the nodes that were recovered in the trees generated by both the neighbour-joining (NJ) and the maximum-likelihood (ML) methods and numbers at nodes represent bootstrap values (NJ/ML) based on 1000 replicated datasets. Only values above 50% are shown. Bar, 0.1 substitutions per nucleotide position.

Fig. 3 in A report of 42 unrecorded actinobacterial species in Korea

Fig. 3. Neighbor-joining phylogenetic tree, based on 16S rRNA gene sequences, showing the relationships between the strains isolated in this study and their relatives of the order Micrococcales in the class Actinobacteria. Asterisks indicate that the corresponding branches were also recovered in both the maximum-likelihood and maximum-parsimony trees. Bootstrap values (>60%) are shown at the branching points. Bar, 0.01 substitutions per nucleotide position.

Fig. 1 in A report of 42 unrecorded actinobacterial species in Korea

Fig. 1. Transmission electron micrographs or scanning electron micrographs of cells of the strains isolated in this study. Strains: 1, C1-45; 2, C6-3; 3, BE5-3; 4, LPB0127; 5, YC6-12; 6, YC7-20; 7, AR23308; 8, YHJ2; 9, JGM01; 10, LPB0135; 11, 6228; 12, 10038; 13, Gsoil 608; 14, 5189; 15, UL003; 16, HMF7422; 17, MMS16-CNU056; 18, ATS3307; 19, PTS2402; 20, AMA3210; 21, Gsoil 163; 22, CAH-3; 23, 2JSS04; 24, J52; 25, Gsoil 1513; 26, PMA2201; 27, ZOD2-24; 28, LPB0133; 29, PMA2305; 30, LPB0125; 31, IMCC25640; 32, 5187; 33, PMA3209; 34, YC4-25; 35, YC3-14.

Fig. 2 in First report of Dryopteris namegatae and reexamination of D. hangchowensis (Dryopteridaceae) from Korea

Fig. 2. Illustrations of Dryopteris namegatae (Sa. Kurata) Sa. Kurata. A. Habit. B. Scales on base of stipe. C. Scales on middle of stipe. D. pinna. E. Spore. F. Scales on rachis.

Fig. 4 in First report of Dryopteris namegatae and reexamination of D. hangchowensis (Dryopteridaceae) from Korea

Fig. 4. Illustrations of Dryopteris hangchowensis Ching. A. Habit. B. Scales on stipe. C. Cross section of stipe. D. Pinna. E. Spore. F. Scales on rachis.

Fig. 1 in First report of Dryopteris namegatae and reexamination of D. hangchowensis (Dryopteridaceae) from Korea

Fig. 1. Photographs of Dryopteris namegatae (Sa. Kurata) Sa. Kurata, taken in Dororeum, Hallimeup, Jeju-si, Jeju-do on 8 Sept. 2012 by Sun-yeul Ko. A. Habit. B. Scale on rachis and immersed vein. C. Abaxial surface with sori and indusium.

Fig. 3 in First report of Dryopteris namegatae and reexamination of D. hangchowensis (Dryopteridaceae) from Korea

Fig. 3. Photographs of Dryopteris hangchowensis Ching, taken in Mudeungsan, Gwangju-jikhalsi on 24 Oct. 2012 by Ganghyup Lee. A. Habit. B. Abaxial surface with sori and indusium. C. Lateral pinna of upper lamina.

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Fig. 3 in The first report of hydatid disease (Echinococcus granulosus) in an Australian water buffalo (Bubalus bubalis)

Fig. 3. Section of a PAS-stained hepatic hydatid cyst from a 3 year old female water buffalo from a farm in New South Wales, Australia (LL = laminated layer; GL = germinal layer (detatched, normally closely applied to the laminated layer).

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Fig. 1 in The first report of hydatid disease (Echinococcus granulosus) in an Australian water buffalo (Bubalus bubalis)

Fig. 1. One of the buffalo grazing paddocks abutting State Forest containing populations of wild dogs (dingoes and/or dingo/domestic dog hybrids).

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Fig. 2. Pulmonary hydatid cyst from a 3 year old female water buffalo from a in The first report of hydatid disease (Echinococcus granulosus) in an Australian water buffalo (Bubalus bubalis)

Fig. 2. Pulmonary hydatid cyst from a 3 year old female water buffalo from a farm in New South Wales, Australia.

Fig. 3 in A report of 31 unrecorded bacterial species in South Korea belonging to the class Gammaproteobacteria

Fig. 3. Neighbor-joining phylogenetic tree, based on 16S rRNA gene sequences, showing the relationships between the strains isolated in this study and their relatives of the order Enterobacteriales in the class Gammaproteobacteria. Bootstrap values (>50%) are shown at branching points. Filled circles indicate that the corresponding nodes were also recovered in the trees generated with the maximum-likelihood and maximum-parsimony algorithms, while open circles indicate that the corresponding nodes were also recovered in the tree generated with one of these algorithms. Bar, 0.01 substitutions per nucleotide position.

Fig. 2 in A report of 31 unrecorded bacterial species in South Korea belonging to the class Gammaproteobacteria

Fig. 2. Neighbor-joining phylogenetic tree, based on 16S rRNA gene sequences, showing the relationships between the strains isolated in this study and their relatives of the order Pseudomonadales in the class Gammaproteobacteria. Bootstrap values (>50%) are shown at branching points. Filled circles indicate that the corresponding nodes were also recovered in the trees generated with the maximum-likelihood and maximum-parsimony algorithms, while open circles indicate that the corresponding nodes were also recovered in the tree generated with one of these algorithms. Bar, 0.01 substitutions per nucleotide position.

Fig 2 in A report of 21 unreported bacterial species in Korea, belonging to the Betaproteobacteria

Fig 2. Phylogenetic tree based on 16S rRNA gene sequence comparisons, showing the relationship between the isolated 21 strains in this study and the notable type species from class Betaproteobacteria. The tree was mainly reconstructed using the neighbour-joining algorithm (NJ). Maximum-likelihood (ML) and maximum-parsimony (MP) algorithms were applied for additional comparison. Filled diamonds indicate branches present in the phylogenetic trees generated using the three different methods. Numbers on the nodes (>70%) represent bootstrap values as percentages of 1000 replicates (NJ/ML/MP). Escherichia coli ATCC 11775T (JMST01000030) was used as an outgroup. Values <70% are not shown at the branch points. Bar, 0.02 accumulated changes per nucleotide.

Fig. 1 in A report of 21 unreported bacterial species in Korea, belonging to the Betaproteobacteria

Fig. 1. Transmission electron micrographs or scanning electron micrographs of cells of the strains isolated in this study. Strains: 1, MWS- 11; 2, HME9229; 3, HME9289; 4, HME94085; 5, HME9441; 6, HME9445; 7, DT6-05; 8, SR2-07; 9, SR4-06; 10, W9-3-1; 11, W3-2-5; 12, W6-4-1; 13, MY2F10; 14, MY2F9; 15, JJ9008; 16, JJ9012; 17, 2013 C3; 18, 2013 C24; 19, 2013 Y1; 20, NC3Y-10-3; 21, MS6Y-8-9.

Fig. 4 in A report of 31 unrecorded bacterial species in South Korea belonging to the class Gammaproteobacteria

Fig. 4. Neighbor-joining phylogenetic tree, based on 16S rRNA gene sequences, showing the relationships between the strains isolated in this study and their relatives of the class Gammaproteobacteria. Bootstrap values (>50%) are shown at branching points. Filled circles indicate that the corresponding nodes were also recovered in the trees generated with the maximum-likelihood and maximum-parsimony algorithms. Bar, 0.01 substitutions per nucleotide position.

Fig. 1 in A report of 31 unrecorded bacterial species in South Korea belonging to the class Gammaproteobacteria

Fig. 1. Transmission electron micrographs or scanning electron micrographs of cells of the strains isolated in this study. Strains: 1, DT1-03; 2, DT1-04; 3, DT1-05; 4, DT5-05; 5, ST6-03; 6, DR3-01; 7, SR3-03; 8, SR4-03; 9, SR6-02; 10, Gsoil 852; 11, MBM1; 12, MDY2F18; 13, MBB2-1; 14, JJ9010; 15, IMCC1859; 16, IMCC20105; 17, IMCC20160; 18, IMCC20164; 19, IMCC20180; 20, MWS24; 21, NMWL17; 22, SD19; 23, B-12; 24, SJ3-2; 25, JW17; 26, HME9287; 27, HME9331; 28, HME9414; 29, HME9429; 30, WS85; 31, WW126.