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Figure 1 in First record of Oligosarcus itau (Characiformes: Characidae) outside the type locality, and second after the description

Figure 1. Known geographical distribution of Oligosarcus itau, Río Bermejo basin in Salta, and Jujuy province, northwestern Argentina. Red circle is the type locality, yellow circles are new records herein reported.

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Fig. 1 in Change Of Morphometric And Allometric Patterns On Wings Of Banded Demoiselle (Calopteryx Splendens) Males In Case Of Ecologically Different Watercourse Types

Fig. 1. The typical appearance of watercourse types in Northeast Hungary (A = creek, B = brook, C = stream, D = little river, E = medial river). (Photo: Miskolczi, M.)

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Fig. 5 in Change Of Morphometric And Allometric Patterns On Wings Of Banded Demoiselle (Calopteryx Splendens) Males In Case Of Ecologically Different Watercourse Types

Fig. 5. PCA with watercourse type, for fore and hind wing (1. component = 77.66%; 2. component = 11.70%) (filled symbols: fore wing, empty symbols: hind wing). Symbols:

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Fig. 2 in Change Of Morphometric And Allometric Patterns On Wings Of Banded Demoiselle (Calopteryx Splendens) Males In Case Of Ecologically Different Watercourse Types

Fig. 2. Measuring points on the right fore wing of Calopteryx splendens males (A = landmarks related to size and shape measurements, B = landmarks related to measurements on

Fig 4 in Using mating-type loci to improve taxonomy of the Tuber indicum complex, and discovery of a new species, T. longispinosum

Fig 4. Phylogenetic relationships among Asian black truffles based on MAT1-1-1 and MAT1-2-1 sequences. The phylogram was obtained by maximum likelihood inference under the TN93 model. SH-aLRT values and Bayesian posterior probabilities are shown as ML/BPP. https://doi.org/10.1371/journal.pone.0193745.g004

Fig 3 in Using mating-type loci to improve taxonomy of the Tuber indicum complex, and discovery of a new species, T. longispinosum

Fig 3. Relative frequencies of asci with one to six ascospores per ascus for the studied taxa. https://doi.org/10.1371/journal.pone.0193745.g003

Fig 2 in Using mating-type loci to improve taxonomy of the Tuber indicum complex, and discovery of a new species, T. longispinosum

Fig 2. Ascospore spine height of four-spored asci (A) and width of spine bases (B), for the studied taxa. Different letters above boxes indicate significant differences between mean according to Tukey–Kramer honestly significant difference test (P <0.01). https://doi.org/10.1371/journal.pone.0193745.g002

Fig 6 in Using mating-type loci to improve taxonomy of the Tuber indicum complex, and discovery of a new species, T. longispinosum

Fig 6. Tuber longispinosum photographs (holotype, TFM: S17009). A. Dried ascomata (bar = 1 cm). B. Fruit bodies photographed in the field. C. Peridial warts, (bar = 3 mm). D. Asci and ascospores (bar = 30 μm). E. Ascospore (bar = 10 μm). F. Peridium in cross section (bar = 50 μm). https://doi.org/10.1371/journal.pone.0193745.g006

Fig 1 in Using mating-type loci to improve taxonomy of the Tuber indicum complex, and discovery of a new species, T. longispinosum

Fig 1. SEM images of ascospores for Asian black truffles, showing the details of ornamentation. A–C: Tuber longispinosum (A: K70, B: K209, C: K466), D–F: Tuber sp. 6 (D: K152, E: S4, F: S23), G–I: T. formosanum (G: HKAS48268 paratype, H: HKAS62628 holotype, I: HKAS79547), J–L: T. himalayense (J: HP1-3, K: MY5-1, L: SHD1-1- 1), M–O: T. indicum (M: YSH1-8, N: YR1-4, O: HD6-16). Bars = 10 μm. https://doi.org/10.1371/journal.pone.0193745.g001

Fig 7 in Using mating-type loci to improve taxonomy of the Tuber indicum complex, and discovery of a new species, T. longispinosum

Fig 7. Tuber himalayense photographs (TFM: S17015). A. Ascomata (bar = 1 cm). B. Peridial warts, (bar = 3 mm). C. Asci and ascospores (bar = 30 μm). D. Peridium and glebal tissue in cross section (bar = 50 μm). E. Ascospore (bar = 10 μm). https://doi.org/10.1371/journal.pone.0193745.g007

Fig. 8 in Centrohelid Heliozoans (Centroplasthelida Febvre-Chevalier et Febvre, 1984) from Different Types of Freshwater Bodies in the Middle Russian Forest-steppe

Fig. 8. Dendrogram showing the Bray-Curtis similarity (%) of studied microbiotopes by species diversity of centrohelids. Abbreviations: p.d.s – plant debris and silt; pt – peat from mire's lakes; sn – sand; sph – Sphagnum from hollows; wt – water column.

Fig. 1 in Centrohelid Heliozoans (Centroplasthelida Febvre-Chevalier et Febvre, 1984) from Different Types of Freshwater Bodies in the Middle Russian Forest-steppe

Fig. 1. Morphology of living cells of some observed centrohelid species (DIC): A – Acanthocystis nichollsi; B – A. pectinata (from plant debris and silt of Usman' River); C – A. turfacea (from plant debris and silt of Lake Chistoye); D – Raphidocystis symmetrica (from plant debris and silt of Lake Chistoye); E – Choanocystis aculeata (from sand of Lake Maklok); F – Raphidiophrys capitata (from sand of Lake Maklok). Abbreviations: ax – axopodia; pr – protoplast; sc – scales. Scale bar: 20 µm.

Fig. 7 in Centrohelid Heliozoans (Centroplasthelida Febvre-Chevalier et Febvre, 1984) from Different Types of Freshwater Bodies in the Middle Russian Forest-steppe

Fig. 7. Morphology of observed scales of unidentified species (TEM): A–C – Heterophrys-like organism (A – from plant debris and silt of Usman' River; B, C – from plant debris and silt of Lake Krugloye; A – whole cell; B, C – spicules), D–F – unidentified Centrohelea sp. (from water column of Lake Vosmerka; D – scales of the single cell; E, F – plate scales). Abbreviations: sp – spicules. Other abbreviation as in Fig. 1. Scale bars: A, D – 10 µm; B, C, E, F – 1 µm.

Fig. 5. A in Ciliate Community Structure in Vegetation in Eastern Mexico Bromeliads of Different Types of

Fig. 5. A. Trait loadings of retained components in the PCA axes 1 and 2, (B) for each sampling carried out in the seven localities, and (C) for vegetation type and ciliate species richness according to the principal components of model A, of an ordination based on species richness, two continuous and two categorical functional traits of 24 ciliate species at Eastern Veracruz, Mexico. Model C shows prediction ellipses at 95% confidence interval to delimitate the vegetation types. Numbers in B refer to the localities. SDTF = Semideciduous tropical forest, C = Coffee plantation, MCF = Montane cloud forest, PF = Pinus forest.

Fig. 3 in Ciliate Community Structure in Vegetation in Eastern Mexico Bromeliads of Different Types of

Fig. 3. Dendogram of the Jaccard's similarities among localities based on the unweighted pair-group method analysis (UPGMA). For the name of the localities see table 1.

Fig. 2 in Ciliate Community Structure in Vegetation in Eastern Mexico Bromeliads of Different Types of

Fig. 2. Average of water temperature of the samples in relation to the localities were samples were collected. Bars indicate standard deviation.

Fig. 1. A in Ciliate Community Structure in Vegetation in Eastern Mexico Bromeliads of Different Types of

Fig. 1. A. Location of the seven localities of the study. B. Schematic representation of the vegetation from the mountain region to the seashore in east Veracruz, Mexico. L = locality, 1 = La Joya, Acajete; 2 = Santuario de Bosque de Niebla, Xalapa; 3 = Coffee plantation La Onza, Coatepec; 4 = Coffee plantation Arcos Vegas y Rincón de Yeguas, Tuzamapan; 5 = Tlacuitlapa, Jalcomulco; 6 = Unidad de Manejo Ambiental Nace El Río, Descabezadero, Actopan; 7 = Centro de Investigaciones Costeras La Mancha (CICOLMA), Actopan.

Fig. 6 in Centrohelid Heliozoans (Centroplasthelida Febvre-Chevalier et Febvre, 1984) from Different Types of Freshwater Bodies in the Middle Russian Forest-steppe

Fig. 6. Morphology of observed scales of Raineriophrys genera (A–C, E, F, I–L – TEM; D, G, H – SEM): A–D – R. echinata (A–C – from peat of Sphagnum bog Klukvennoye-2; D – from Sphagnum of Sphagnum bog Klukvennoye-3), E–H – R. erinaceoides (E, F – from water column of Lake Vosmerka; G, H – from plant debris and silt of Lake Cherepashye), I–L – R. fortesca (I – Vosmerka, J–L – Cherepashye). E, I – scales of the single cell; A–D, F–H, J–L – spine and plate scales. Abbreviations as in Fig. 2, 5. Scale bars: A, E, I – 10 µm; B–D, F – 5 µm; G, H, J–L – 1 µm.

Fig. 9 in Centrohelid Heliozoans (Centroplasthelida Febvre-Chevalier et Febvre, 1984) from Different Types of Freshwater Bodies in the Middle Russian Forest-steppe

Fig. 9. Dendrogram showing the Bray-Curtis similarity (%) of studied water bodies by species diversity of centrohelids.