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Figs 85–95 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 85–95. Epipharynx (85, 89, 93), apex of corypha (lateral view) (86, 90) and aedeagus (dorsal and lateral view) (87–88, 91–92, 94–95) of: 85–88 = Ammoecius franzi (PETROVITZ, 1964), 89–92 = A. numidicus MULSANT, 1851, 93–95 = A. incultus (PETROVITZ, 1961)

Figs 53–64 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 53–64. Epipharynx (53, 57, 61), apex of corypha (lateral view) (54, 58, 62) and aedeagus (dorsal and lateral view) (55–56, 59–60, 63–64) of: 53–56 = Ammoecius rugifrons AUBÉ, 1850, 57–60 = A.

Figs 49–52 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 49–52. Habitus of: 49 = Ammoecius muchei (PETROVITZ, 1962) (male, length 6.0 mm, Turkey: Vil. Kastamonu, Kastamonu env.), 50 = A. satanas (CARPANETO, 1976) (male, length 7.0 mm, Turkey: Vil. Antalya, 40 km S of Akseki, 3 km S Fersin), 51 = A. felscheanus REITTER, 1904 (male, length 3.5 mm, Algeria: Oran prov., Oued-Imbert), 52 = A. dentatus SCHMIDT, 1908 (male, length

Figs 25–36 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 25–36. Epipharynx (25, 29, 33), apex of corypha (lateral view) (26, 30, 34) and aedeagus (dorsal and lateral view) (27–28, 31–32, 35–36) of: 25–28 = Ammoecius elevatus (OLIVIER, 1789), 29–32 = A. satanas (CARPANETO, 1976), 33–36 = A. meurguesae CLÉMENT, 1975

Figs 15–20. 15 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 15–20. 15 = epipharynx of Ahermodontus bishoffi (VŠETEČKA, 1939), 16 = epipharynx of Ammoecius eli (PETROVITZ, 1961). A. dogueti (BARAUD, 1980): 17 = epipharynx, 18 = apex of

Figs 37–48 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 37–48. Epipharynx (37, 41, 45), apex of corypha (lateral view) (38, 42, 46) and aedeagus (dorsal and lateral view) (39–40, 43–44, 47–48) of: 37–40 = Ammoecius naviauxi (BARAUD, 1971), 41–44 = A. muchei (PETROVITZ, 1962), 45–48 = A. brevis ERICHSON, 1848

Figs 5–14 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 5–14. Vladimirellus socors (BALTHASAR, 1967): 5 = epipharynx, 6 = elytral sculpture, 7–8 = aedeagus (dorsal and lateral view). Ahermodontus ambrosi PARDO ALCAIDE, 1936: 9 = epipharynx, 10–11 = aedeagus (dorsal and lateral view). A. marini BÁGUENA, 1930: 12 = epipharynx, 13–14 =

Figs 21–24 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 21–24. Habitus of: 21 = Ammoecius eli (PETROVITZ, 1961) (female, length 5 mm, Iraq: Mesopotam., Hilleh), 22 = A naviauxi (BARAUD, 1971) (male, length 5.5 mm, Syria: Slennfé), 23 = A. dogueti (BARAUD, 1980) (male, length 6.0 mm, Algeria: Djurdjura, Chemin lac Goulmine), 24 = A. elevatus (OLIVIER, 1789) (male, length 7.0 mm, France: Var, S.te-Baume)

Figs 1–4 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)

Figs 1–4. Habitus of: 1 = Vladimirellus socors (BALTHASAR, 1967) (male, length 4.0 mm; Russia: Siberia Thomsk), 2 = Ahermodontus bishoffi (VŠETEČKA, 1939) (female, length 4.5 mm; Albania: Logara), 3 = A. marini BÁGUENA, 1930 (male, length 4.0 mm; Spain: Castellón, Onda), 4 = A.

FIGURE 3 in Convergent responses of fish belonging to different feeding guilds to sewage pollution

FIGURE 3 | Distribution of the piscivorous species Hoplias intermedius (red points) and the detritivorous species Hypostomus francisci (blue points) in the bi-plot space by study regions: A. Upper RV, B. Middle RV, C. Lower RV and D. Control sites. Resources: GR = Grasses; RV= Riparian vegetation; PE = periphyton; SW = Sewage (before treatment); AL = filamentous algae and FS = Fish.

FIGURE 2 in Convergent responses of fish belonging to different feeding guilds to sewage pollution

FIGURE 2 | Variation in the isotopic composition of carbon (A. and C.) and nitrogen (C. and D.) in the piscivorous species Hoplias intermedius (A. and C.) and the detritivorous species Hypostomus francisci (B. and D.) among the studied regions.

FIGURE 1 in Convergent responses of fish belonging to different feeding guilds to sewage pollution

FIGURE 1 | Sampling network in the rio das Velhas basin, Minas Gerais, Brazil. Sampling sites at rio das Velhas main stem (RV-01 to RV- 05), rio Taquaraçu (TQ); rio Jaboticatubas (JB); rio Cipó (CP1 and CP2); rio da Onça (ON); rio Bicudo (BI); rio Curimataí (CU); and Sewage Treatment Plants (STP's).

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Figure 1 in An investigation on the chloroplast and nuclear genomes of taxa belong to the subgenus Dracunculus (Bess.) Rydb. of Artemisia L. (Asteraceae) in Turkey

Figure 1. Geographic distribution of four species of the subgenus Dracunculus in Turkey (A. campestris (), A. marschalliana (), A. araratica () and A. scoparia () (Civelek et al., 2010, Kursat 2010).

Fig. 3 in Report of 22 unrecorded bacterial species in Korea belonging to phylum Bacteroidetes, discovered during surveys in 2018

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 Bacteroidales, Balneolales, Chitinophagales, Cytophagales and Sphingobacteriales in the class Bacteroidetes. 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, 0.05 substitutions per nucleotide position.

Fig. 1 in Report of 22 unrecorded bacterial species in Korea belonging to phylum Bacteroidetes, discovered during surveys in 2018

Fig. 1. Transmission electron micrographs or scanning electron micrographs of cells of the strains isolated in the study. Strains: 1, LPB0213; 2, MaG24; 3, Wi-47; 4, GA076; 5, KYW1525; 6, Ast28; 7, HMF5202; 8, 18S4T3; 9, 18H1T5; 10, 18H3M2; 11, BT43; 12, BO204; 13, 18S4P11; 14, 18H3V6; 15, 18N3G15; 16, 18N3V8; 17, SC115; 18, HMF9181; 19, SC71; 20, HMF9088; 21, BO167; 22, 18SBM11.

Fig. 5 in Report of 39 unrecorded bacterial species in Korea belonging to Gammaproteobacteria

Fig. 5. 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, 0.02 substitutions per nucleotide position.

Fig. 2 in Report of 39 unrecorded bacterial species in Korea belonging to 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 Aeromonadales and Alteromonadales 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, 0.02 substitutions per nucleotide position.

Fig. 3 in A report on 24 unrecorded bacterial species of Korea isolated in 2016, belonging to the orders Rhizobiales and Sphingomonadales in the class Alphaproteobacteria

Fig. 3. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences showing the relationship between the strains isolated in this study and their relatives in the Sphingomonadales of the Alphaproteobacteria. Bootstrap values (expressed as percentages of 1000 replications) over 70% are shown at nodes for neighbour-joining, maximum parsimony, and maximum likelihood methods, respectively. Filled circles and open circles indicate that the corresponding nodes were recovered by all treeing methods and by two treeing methods, respectively. Bootstrap values (>70%) are shown at nodes. Bar, 0.02 substitutions per nucleotide position.

Fig. 3 in Report of 39 unrecorded bacterial species in Korea belonging to 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 Arenicellales, Vibrionales and Xanthomonadales 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, 0.02 substitutions per nucleotide position.

Fig. 1 in Report of 39 unrecorded bacterial species in Korea belonging to Gammaproteobacteria

Fig. 1. Transmission electron micrographs or scanning electron micrographs of cells of the strains isolated in the study. Strains: 1, 4003; 2, 4231; 3, 7026; 4, 7034; 5, 9023; 6, BE6-1; 7, CAU 1046; 8, CAU 1335; 9, DS041; 10, EC2D12; 11, GM22; 12, Gsoil 3009; 13, HMF7415; 14, HMF8002; 15, HMF8004; 16, HMF8044; 17, IMCC25635; 18, IMCC25639; 19, IMCC25642; 20, IMCC25643; 21, IMCC25647; 22, IMCC25652; 23, KB012; 24, LGGG06; 25, LPB0132; 26, LPB0153; 27, LPB0156; 28, LPB0159; 29, POB9; 30, SFD22; 31, SN5; 32, SN10; 33, UL158; 34, UL222; 35, UL498-1; 36, UL506; 37, YC7-24; 38, YHY1; 39, ZOD21.