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346 results for “Echinoderes”
Fig. 4 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Effects of direct transfer from FW to SW on protein abundance (A) and activity (B) of Na+/K+-ATPase (NKA) in kidneys of the green spotted pufferfish. The asterisks indicate significant differences (P <0.05) using Dunnett's multiple-comparison test following a one-way ANOVA. Values are means ± SEM (n = 5). NKA protein decreases gradually within 6 h post-transfer and significantly decreases after 12 h post-transfer. NKA activity decreases significantly within 3 h post-transfer returns to the initial level at 6 h, and decreases significantly after 12 h post-transfer.
Fig. 3 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 3. Effects of direct transfer from FW to SW on protein abundance (A) and activity (B) of Na+/K+-ATPase (NKA) in gill epithelia of the green spotted pufferfish. The asterisks indicate a significant difference (P <0.05) using Dunnett's multiple-comparison test following a one-way ANOVA. Values are means ± SEM (n = 5). NKA protein and activity increase significantly within 3 h post-transfer.
Fig. 2 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 2. Representative immunoblots of the Na+/K+-ATPase (NKA) α-subunit of the green spotted pufferfish gill and kidney sampled during a time-course following transfer from FW to SW. Single immunoreactive bands were observed with α5 monoclonal antibody corresponding to a molecular mass of approximately 100 kDa. Arrows indicate immunoreactive bands at approximately 100 kDa.
Fig. 8 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 8. Frequency distribution of the s statistic obtained by simulated gene trees under two different scenarios and values for Ne. Left column, the after glaciation subdivision model (AGSM). Right column, the recent subdivision model (RSM). Segmented line shows where the observed s value (s = 11) falls.
Fig. 7. Bayesian Skyline Plot analysis showing population size over time. The x in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 7. Bayesian Skyline Plot analysis showing population size over time. The x-axis is the time to the present in years, while the y-axis is the product between the effective population size (Ne) and the generation length (t) in a log scale. The mean estimate (black solid line) and 95% highest probability density limits (grey area) are shown.
Fig. 6 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 6. Mismatch distribution analysis based on pairwise comparisons between 62 mitochondrial DNA sequences.
Fig. 4 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Bayesian phylogenetic tree based on 62 mitochondrial DNA sequences (Cyt b and CR combined). Colored circles in front of tips represent area of origin as shown in figure 1. Tip labels refer to individual codes as in table 1.
Fig. 3 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 3. Frequency distribution of the genetic diversity (π) in the Valdivia basin estimated by bootstrap. Ten thousand samples using 13 randomly chosen individuals each time were used to obtain the distribution. Dashed line indicates the observed nucleotide diversity for Area III. A, bootstrap with replacement. B, bootstrap without replacement. N, number of individuals; S, haplotype richness; H, haplotype diversity; π, nucleotide diversity.
Fig. 5 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 5. Haplotype network based on combined Cyt b and CR regions. Size of the haplotype represents its frequency. Colors represent sampling Area.
Fig. 1 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 1. Time-course changes of plasma osmolality, Cl-, and Na+ in the green spotted pufferfish transferred directly from FW to SW. The asterisks indicate a significant difference (P <0.05) using Dunnett's multiple-comparison test following a one-way ANOVA. Values are means ± SEM (n = 5). Significant increase in osmolality and Cl- occurred within 3 h, and in Na+, within 6 h post-transfer.
Fig. 5 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 5. Variance partitioning analysis. Venn diagram showing the independent and shared variance explained by local factors (L), landscape descriptors (LA) and spatial structure (S) related to Lithobates catesbeianus abundance.
Fig. 2 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 2. Models tested in coalescent simulations. Left, the after glaciation subdivision (AGS) model. Right, the recent subdivision (RS) model. Roman numbers on tips indicate main Areas in the basin.
Fig. 1 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 1. Map showing location sampling and defined Areas within the Valdivia Basin. Main Areas are separated by short straight dashed lines. Population codes (numbers) are described in Table 1. Long dashed line indicates the western limit of the LGM ice sheet based on Hulton et al. (2002).
Fig. 4 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Relationship between Lithobates catesbeianus abundance (transformed in logarithm) and local descriptors selected by the model: (a) water surface area (m2) and (b) hydroperiod (P - permanent; T - temporary).
Fig. 1 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 1. (a) Location of Turvo State Park (TSP) in the far northwest of Rio Grande do Sul state (RS), Brazil. (b) Sampling design in Turvo State Park and surroundings areas: circles and respective numerations represent sampled waterbodies; dashed lines delineate the two transects that represent the spatial-environmental gradient of sampled breeding sites.
Fig. 3 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 3. Relationship between bullfrog abundance and forest edge distance (m) in a forest-edge-agriculture gradient. Negative values represent the distances between waterbodies within protected areas and positive values represent adjacent agricultural areas. Forest edge is represented by light gray line (or number zero).
Fig. 3 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 3. The divergence times (million years ago) of Rhodeus ocellatus in East Asia. The results estimated by 1.05% per site per million years of the evolutionary rate are shown at the main nodes with the 95% highest posterior densities (HPD) intervals in the parenthesis. The ranges of 95% HPD intervals are represented by the gray bars. Numbers in reverse color at main nodes correspond to Additional file 3. The spatial distributions of the lineages are represented in figure 1 with the same color usage.
Fig. 4 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Neighbor-joining (NJ) tree for cytochrome oxidase subunit I (COI) gene sequences of 11 species of Sillaginidae. The NJ tree was constructed under the K2P model using Sillaginodes punctata as outgroup. Bootstrap support values of> 50% from 1000 replicates are shown.
Fig. 3 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 3. Swim bladders of 7 Sillago species. (A) S. shaoi sp. nov., (B) S. sihama, (C) S. sinica, (D) S. indica (Kaga and Ho 2012), (E) S. parvisquamis (McKay 1992), (F) S. intermedius (McKay 1992), (G) S. caudicula (Kaga et al. 2010). AE, anterior extension; ASAE, anterior sub-extension of anterolateral extension; PSAE, posterior sub-extension of anterolateral extension; LP, lateral processes; DLP, duct-like process; PE, posterior extension.
Fig. 12 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 12. Echinoderes serratulus sp. nov., scanning electron micrographs. A, segments 5 and 6, lateral view; B, segments 8 and 9, lateroventral view; C, segment 6, sublateral view; D, segment 9, sublateral view; E, segments 9-11 in female, dorsal view; F, segments 10 and 11 in male, lateral view; G, segments 10 and 11 in female, lateral view. Dashed circles indicate sensory spots. Abbreviations: gco2, type-2 glandular cell outlet; ldt, laterodorsal tubule; ltas, lateral terminal accessory spine; lts, lateral terminal spine; lvt, lateroventral tubule; mlt, midlateral tubule; pe, penile spine; po, pore; si, sieve area; sls, sublateral acicular spine.
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Allen Brain Atlas
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OpenNeuro
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