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346 results for “Echinoderes”
Fig. 3 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 3. The counting zone: (a) A commercial signal float (arrow, 3 m in length) was set to define the counting zone. The size of school was estimated by counting the number of fishes that passed the zone in a given time multiplied by the total time that the entire fishes took to pass the zone. (b) Some school that was not participated in the migration group. In this case the school was photographed to estimate the gross population (a dot on fish indicates the fish was counted).
Fig. 5. A in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 5. A comparison of the mode of appearances: (a) S. spilurus between 2006 and 2009. The spawning aggregation formed two distinct periods of a year between February to April and September to November. Number of fish observed in the earlier period, between the full (open circle) and new (closed circle) moon are shown. (b) The mode of appearance of L. bohar between 2010 and 2013. The aggregation formed every month throughout the year. Representative modes of appearance observed between February and April were shown for direct comparison.
Fig. 4 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Resting areas of Symphorichthys spilurus and Lutjanus bohar. (a) Schematic overview and (b) cross section of resting area. (c) Aerial photo of the resting area of Ss. An arrow shows shot direction of, (d) underwater photograph. (e) Aerial photo of resting area of Lb. An arrow shows shot direction of, (f) underwater photograph.
Fig. 2 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 2. Observation site: southernmost reef of Peleliu Island. The "resting area" where sub-aggregate schools of S. spilurus and L. bohar gather are highlighted in yellow and red, respectively. The spawning ground is marked in white circle.
Fig. 1 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 1. Location of Peleliu Island and two other sites where S. spilurus is known to spawn in Palau.
Fig. 5 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 5. Differentiation between different groups based on the first two principal components of song features (A) and geographical distribution (B). Geographic base map in (B) is from Google Maps (Google, USA). The relationship between principal components and song variables are shown in table 3.
Fig. 6 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 6. Boundary in China between distribution areas of Cuculus optatus and Cuculus saturatus during breeding season. The dashed line is the boundary that Johnsgard (1997) used to separate Cuculus optatus and Cuculus saturatus. The solid line is the boundary suggested by this study. a: Northern mainland China, b: Taiwan Island. Geographic base map is from Google Maps (Google, USA).
Fig. 2 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 2. Frequency distribution (A) and geographical distribution (B) of the note number per syllable in each syllable. The red arrow indicates the quartile. Geographic base map in (B) is from Google Maps (Google, USA).
Fig. 4 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Frequency distribution (A) and geographical distribution (B) of syllable frequency. The red arrow indicates the quartile. Geographic base map in (B) is from Google Maps (Google, USA).
Fig. 2. The 5 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 2. The 5' UTR nucleotide sequence of the Mc1r gene. The maximum length of the 5'UTR is 588 bp. The first ATG codon is boxed. Transcriptional initiation sites are indicated by arrows. Consensus binding sites for SP-1 and AP-2 transcription factors are underlined. The parentheses refer to mouse (M) or rat (R). The CANNTG motifs based on reports from mouse experiments are heavily underlined.
Fig. 1 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 1. Variation in coat color of black-bellied voles (Eothenomys melanogaster). (a) A black color form (Yu2045) sampled at Alishan, location I in the map (b) A brown color form (Yu2014) sampled at Wuling, location IV in the map (c) Alishan habitat (I in the map) with darker soil color (d) Wuling habitat (IV in the map) with lighter soil color (e) Map of Taiwan showing sites of sample collection: Alisan (I), Tataka (II), Guanwu (III), and Wuling (IV); the map inset shows the geographical location of Taiwan (red color) in East Asia.
Fig. 3 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 3. Monthly feeding time variation on different food types. RF= Ripe Fruit, UF= Unripe Fruit, FL= Flowers, ML= Mature Leaves, YL= Young Leaves.
Fig. 1 in Echinoderes blazeji Grzelak & Sørensen 2022, sp. nov.
Fig. 1. This map illustrates the areas where blue marlin samples were taken. The triangle and ellipse symbols indicate sampling sites. EP, eastern Pacific; WNP, western North Pacific; SCS, South China Sea; EI, eastern Indian Ocean.
Fig. 3 in Echinoderes blazeji Grzelak & Sørensen 2022, sp. nov.
Fig. 3. Median joining network of 239 of blue marlin CR haplotypes. Each circle means a unique haplotype, and diameter is proportional to the individual number shading that haplotype.
Fig. 2 in Echinoderes blazeji Grzelak & Sørensen 2022, sp. nov.
Fig. 2. Phylogenetic tree of 239 blue marlins based on CR sequences. Rooted phylogeny of 239 blue marlin CR sequences from maximum likelihood (ML) analysis and Bayesian (BA) analysis. Topologies of ML and BA analyses are similar; differences exist only in those relationships with weak statistical support. Numbers on branches are ML bootstrap values (Those below 70% are not shown) and solid circles on branch nodes indicate statistically robust nodes with posteriori probabilities from partitioned Bayesian analysis ≥ 0.95.
Fig. 4 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Immunoblots of tissues lysates of the control group, the hypoxic group and the restricted group on day 3. The relative protein abundance was detected by immunoblots of extracts from the 1st gill, the 4th gill and the labyrinth organ of T. microlepis. (A) NKA expression within each tissue was not significantly different among the three groups. (B) PCNA expression within each tissue was not significantly different among the three groups. (C) CAII expression was significantly different in the labyrinth organ between the control group and the hypoxic group (asterisk indicates a significant difference, Dunnett's test, P <0.05). 1st gill: first gill, 4th gill: fourth gill, LO: labyrinth organ.
Fig. 5 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 5. Immunoblots of tissue lysates from the control group, the hypoxic group and the restricted group on day 14. The relative protein abundance was detected by immunoblots in the 1st gill, the 4th gill and the labyrinth organ of T. microlepis. (A) NKA expression within each tissue was not significantly different among the three groups. (B) PCNA expression was significantly higher in the 1st gill and the labyrinth organ in the restricted group compared to the control group (asterisk indicates a significant difference, Dunnett's test, P <0.05). (C) CAII expression within each tissue was not significantly different among the three groups. 1st gill: first gill, 4th gill: fourth gill, LO: labyrinth organ.
Fig. 3 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 3. Gill morphology in T. microlepis was observed in the control group, the hypoxic group and the restricted group after 28 days. A, E, and I was the 1st gill; B, F, and J was the 2nd gill; C, G, and K was the 3rd gill; D, H, and L was the 4th gill, which had the larger vessels in the lamellar base. A-D show gills in the control group; E-H show gills in the hypoxic group; I-L show gills in the restricted group. Significant morphological changes were observed in the 4th gill in the restricted group after 28 days (L). The rest of the groups showed no apparent morphological modification among gills. F: filament, L: lamellar, RBC: red blood cell. Scale bar = 50 μm
Fig. 2 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 2. Lengths of the filaments and lamellae among gills from fish was recorded in the control group, the hypoxic group and the restricted group after 14 and 28 days. A-D shows the lengths of the filaments in gills 1 through 4 from the three groups. Within each gill, no significant difference among the three groups was found after 14 and 28 days. E-H shows the lengths of the lamellae in gills 1 through 4 from the three groups. There was a significant difference in the 1st gill in the restricted group after 14 and 28 days (Dunnett's test, P <0.05). Another difference was also observed in the 4th gill in the restricted group after 28 days (Dunnett's test, P <0.05).
Fig. 1 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 1. The frequency of ABR in T. microlepis exposed to normoxia and hypoxia for 14 days. The frequency of ABR in the hypoxic group was significantly higher than that in the control group at days 1, 2, 4, 7, and 14 (asterisk indicates a significant difference between hypoxia and normoxia, t test, P <0.05). The frequency in the hypoxic groups increased to its highest level at day 1 and then gradually decreased to a stable level until the end of the 14-d experiment (Tukey's test, P <0.05).
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OpenNeuro
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