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Fig. 5 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 5. (A–I) Psolus nanoplax sp. nov. Martins & Tavares (MZUSP 589). SEM photomicrographs of the ossicles. (A) knobbed plate from dorsal body (B) supporting rod from dorsal tube feet; (C) "cup-like" plates from sole in dorsal view; (D) "cup-like" multiperforated plates from sole in ventral view; (E) "cup-like" four-holed plates from sole in dorsal view; (F) "cup-like" plates from sole in lateral view (G) knobbed plates from sole and (H–I) knobbed plates from ventral tube feet. Scale bars: A–B = 50 μm; C = 20 μm; D–I =, 30 μm.

Fig. 1. Species trees and alternative constraint convergence topologies. H0 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 1. Species trees and alternative constraint convergence topologies. H0 is the well-accepted species tree. H1, H2, and H3 are three alternate echolocator-converged topologies. H1-control, H2-control and H3-control refer to the constraint convergent topologies of representative non-echolocators (cow, hedgehog, and non-echolocating bats).

Fig. 4 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 4. (A–F) Psolus nanoplax sp. nov. (MZUSP 589, 592). (A) lateral view of holotype preserved in ethanol (note anal cone in white arrow); (B) upper view of [paratype-MZUSP 592] preserved in ethanol (note mouth and anus in black and red arrows, respectively); (C) detail of anal cone [holotype-MZUSP 592] (note anal cone and papillae, in white and red arrows, respectively); (D) detail of dorsal tube feet [holotype-MZUSP 592] (red arrow); (E) detail of lateral scales [paratype-MZUSP 592]; (F) ventral view detail of ambulacral feet [paratype-MZUSP 592], (note the inner and outer rows of tube feet: black and white arrows, respectively); (G) calcareous ring (H) detail of retractor muscle (white arrow) and (I) outline of the calcareous ring [paratype-MZUSP 592]; R, radial plate. IR, interradial plate. Note, only radial plate notched. Scale bars: A = 5 mm; B = 4 mm; C = 500 μm, D = 500 μm, E = 0.5 mm; F = 2 mm; G–I = 500 μm.

Fig. 3 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 3. (A–F) Psolidium lonchostinum sp. nov., holotype (MZUSP 744). SEM photomicrographs of the ossicles. (A) four-holed smooth plate from sole, ventral view; (B) four-holed smooth plate from sole, dorsal view; (C–D) multiperforated smooth plate from sole, dorsal view; (E) four-holed smooth plate from sole, lateral view; (F) rod from ventral tube feet, dorsal view. Scale bars: A–B = 30 μm; C = 40 μm; D–E = 50 μm; F = 80 μm.

Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 2. (A–F) Psolidium lonchostinum sp. nov., holotype (MZUSP 744). SEM photomicrographs of the ossicles. (A) scale from dorsal body wall, showing canals for tube feet (white arrow); (B) smooth plate from dorsal body; (C) branched rods (thorn ossicle) (black arrow); (D) rod from dorsal tube feet; (E–F) knobbed plates from sole. Scale bars: A–B = 50 μm; C = 40 μm; D–F = 50 μm.

Fig. 1 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 1. (A–F) Psolidium lonchostinum sp. nov. (A–D) holotype (MZUSP 744). (A) upper view; (B) detail of dorsal tube feet (black arrow); (C) detail of lateral scales (white arrow); (D) ventral view; detail of ambulacral feet (note the inner and outer rows of tube feet: black and white circles, respectively); (E) paratype (MZUSP 591)) detail of ventral tube feet (black arrow); (F) outline of the calcareous ring [holotype] R, radial plate. IR, interradial plate. Note in F interradial plate entire and radial plate notched. Scale bars: A = 4 mm; D = 2 mm; E = 3 mm; F = 500 μm.

Fig. 3 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 3. Differences in the response of forest specialists (Forest) and open habitat specialists (Open) of ground beetles (Carabidae) to power lines and forests in Poland. Circles and triangles indicate results for power lines and forest interior, respectively. Whiskers represent 95% confidence intervals.

Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 2. Differences in the response of selected insect groups to power lines and forests in investigated study sites in Poland: (a) ground beetles (Carabidae), (b) jewel beetles (Buprestidae), (c) long-horn beetles (Cerambycidae), (d) lady-bird beetles (Coccinellidae), (e) weevils and bark beetles (Curculionidae), (f) click beetles (Elateridae), (g) rove beetles (Staphylinidae), (h) darkling beetles (Tenebrionidae), (i) butterflies (Lepidoptera). Circles and triangles indicate results for power lines and forest interior, respectively. Whiskers represent 95% confidence intervals.

Fig. 1 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 1. Illustration of the study sites: I (a), II (b), III (c), IV (d). For basic characteristics of study sites, see table 1.

Fig. 3 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 3. Convergence of echolocation in Sorex araneus and sophisticated echolocators. (A) Convergence of the sophisticated echolocating bats and simple echolocator Sorex araneus shown by the multilocus concatenated gene tree based on 481 potential convergence contributing amino acid sites in BI method. (B) Multilocus concatenated BI tree based on the whole multilocus concatenated amino acid alignment. (Numbers at internal nodes indicate posterior probability).

Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.

Fig. 2. Radical property changes and convergent/parallel amino acid substitutions in echolocating mammals. Lineages in red, green, and blue indicate echolocating bats, toothed whales, and the common shrew, respectively. Convergent and parallel amino acid substitutions in common shrew and echolocating bat lineages are in pink boxes. Sites with radical property changes in the common shrew and echolocating bats are depicted in red boxes. Sites in light green indicate the convergent and parallel substitutions between common shrew and toothed whales, and sites in green boxes indicate radical property changes.

Fig. 5 in Comparison of sampling methodologies and estimation of population parameters for a temporary fish ectoparasite

Fig. 5. Histograms of emergence counts from the time-series emergence traps. Count bars for each day are subdivided by individual trap.

Fig. 4 in Comparison of sampling methodologies and estimation of population parameters for a temporary fish ectoparasite

Fig. 4. Scatterplot showing total body length in mm versus estimated volume of blood and plasma extracted in Ml. The box-and-whisker plots are centered on the mean body length for each of the three juvenile stages. The box edges are placed at the 2nd and 3rd quartiles for volume estimates and the whiskers show extreme minimum and maximum volumes. The mean estimate of extracted volume by juvenile stage is shown as a labeled dashed-red horizontal line. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Fig. 1 in Comparison of sampling methodologies and estimation of population parameters for a temporary fish ectoparasite

Fig. 1. Traps used in the first study. (A) Small emergence trap, (B) fish-baited emergence trap, (C) fish-baited tripod, (D) open-mesh fish-baited trap and (E) lighted plankton trap. Note that the sample container holding a small French grunt fish for the fish-baited emergence trap (B) and the fish-baited tripod trap (C) are identical units other than the sealed floats attached to the top of the sample container when used with the fish-baited emergence trap.

Fig. 2 in Comparison of sampling methodologies and estimation of population parameters for a temporary fish ectoparasite

Fig. 2. Traps used in the second study. The lighted plankton trap, in the left foreground, stands on short legs—four large emergence traps can be seen in the middleground to the right of the lighted plankton trap. A second lighted plankton trap in the background can be seen towards the center of the frame.

Fig. 3 in Comparison of sampling methodologies and estimation of population parameters for a temporary fish ectoparasite

Fig. 3. Scatterplots of total body length in mm plotted against eye length in mm along the long axis. The upper plot shows measurements for zuphea and the lower plot for praniza. The body length cutoff values separating juvenile stages are shown as a dotted-green line. Gnathiids collected from emergence traps are seen as gold-filled squares and those collected from light traps are presented as purple-filled triangles. Differences in the ontological sampling bias of these two trap designs can be seen by comparing the two scatterplots. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Fig. 6 in Comparison of sampling methodologies and estimation of population parameters for a temporary fish ectoparasite

Fig. 6. Histograms of trap counts by sample day and juvenile stage. The upper histograms show counts from emergence traps and the lower histograms show counts from light traps. Mean count for each histogram is shown as a dashed horizontal line. See text for an explanation of the number of sampling days shown in each plot.

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Fig. 3 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 3. Single nucleotide polymorphisms in the ND2 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Speciesspecific SNPs are shown in bold.

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Fig. 1 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 1. Single nucleotide polymorphisms in the Cox1 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Italicized numbers represent the position number from a previously published partial sequence of the B. columnaris Cox1 gene (Franssen et al., 2013). Species-specific SNPs are shown in bold.