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Fig. 2 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 2. Spatial filter representing the spatial autocorrelation (Moran's I) related to the distributional pattern of Lithobates catesbeianus measured in multiple classes of distance (km) between sampled waterbodies.
Fig. 2 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 2. Echinoderes regina sp. nov., camera lucida drawings. A, B, Holotype, female (ZIHU-5045), entire animal, dorsal and ventral views, respectively; C, D, allotype, male (ZIHU-5046), segments 9-11, dorsal and ventral views, respectively. White, grey, and black circles or ovals indicate sensory spots, type-1 glandular cell outlets, and type-2 glandular cell outlets, respectively. Abbreviations: gco1, type-1 glandular cell outlet; gco2, type-2 glandular cell outlet; ldt, laterodorsal tubule; ltas, lateral terminal accessory spine; lts, lateral terminal spine; lvt, lateroventral tubule; mds, middorsal acicular spine; ps, penile spine; si, sieve plate; sls, sublateral acicular spine; slt, sublateral tubule; ss, sensory spot.
Fig. 1 in Echinoderes blazeji Grzelak & Sørensen 2022, sp. nov.
Fig. 1. Temperatures of experimental nests in relation to time of day. Temperature means (± SE) for experimentally heated (black) and control nests (white) of Great Tits in relation to time of day (day-time: 07:00-20:00; night-time: 20:00-07:00). We show data for two consecutive years: 2011 (dots) and 2012 (triangles). Sample sizes above error bars refer to number of nests.
Fig. 5 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 5. Estimated egg-development period. (a) Estimated by equation 1: D (T - t) = k; (b) Estimated by equation 2 (Ikemoto and Takai 2000): (DT) = k + tD.
Fig. 1 in Echinoderes blazeji Grzelak & Sørensen 2022, sp. nov.
Fig. 1. Responses of Green Treefrogs to presentation of conspecific calls (Con), heterospecific calls (Het), white noise (N) and silence (S). (a) The proportion of frogs that reached the arena wall was similar for the different treatment stimuli. (b) Orientation (angular deviation; least square means ± SE) was not directional towards the speaker presenting treatment stimuli; speaker position at 0 degree. (c) Approach latency was similar across treatments; (d) Polar diagrams showing the locations at which frogs touched the arena wall in relation to the position of the speaker (at 0 degree; top of diagram); each dot represents one frog.
Fig. 10 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 10. Normal distributions of: (a) Ambient water temperature (bold line), that at the time S. spilurus (circles), and L. bohar (triangles) spawn. (b) Current velocity of spawning site (bold line), that at the time S. spilurus (circles), and L. bohar (triangles) spawn, (c) Current direction of spawning site (bold line), that at the time S. spilurus (circles), and L. bohar (triangles) spawn. Above data were recorded between February 2 and April 18, 2015.
Fig. 1 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 1. Map of the sampling localities and the population structures of Rhodeus ocellatus in East Asia. Black circles refer to sampling localities and Pie charts refer to lineage compositions in each locality with the numbers correspond to the locality numbers of Additional file 1. Roman numerals represent the biogeographic regions: Northeastern (I), Yellow River (II), Lower Yangtze (III), Upper-Middle Yangtze (IV), Southern (V), Japan (VI), Korea (VII), and Taiwan (VIII) region. The colors used in the pie charts correspond to the lineages in figure 2.
Fig. 4 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Daily mean temperature and humidity in the Pandanus odoratissimus dominated coastal forest on Iriomote-jima Island.
Fig. 4. Minimum spanning network and mismatch distribution from cyt b in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 4. Minimum spanning network and mismatch distribution from cyt b DNA sequences of Rhodeus ocellatus in each lineage. The colors correspond to the lineage in figure 2. The size of each circle represents the number of specimens of each haplotype. The small, open circle between different haplotypes represents the number of mutations. The number of mutations> 8 is shown as the mutation number beside the traverse lines. The results of mismatch distribution are shown in the histograms. The abscissa and ordinate of the histograms indicate the number of pairwise difference between specimens and the frequency of each value, respectively. The black and gray bars represent the frequency distribution of the observed and expected pairwise difference respectively under the sudden expansion model.
Fig. 5. Demographic inference from cyt b in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 5. Demographic inference from cyt b sequences of Rhodeus ocellatus in East Asia. (A) Mismatch distribution of total population. The abscissa and ordinate of the histograms indicate the number of pairwise difference between specimens and the frequency of each value, respectively. The black and gray bars represent the frequency distribution of the observed and expected pairwise difference respectively under the sudden expansion model. (B) Bayesian skyline plot (BSP) of total population estimated by 1.05% per site per million year of evolutionary rate. The black line indicates the mean curve of BSP. The dotted line indicates the 95% highest posterior density intervals of the BSP. The x-axis indicates the time (million years ago, mya). The y-axis is the estimated effective population size.
Fig. 11 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 11. Diagram of mouth cone, introvert, and placids in Echinoderes serratulus sp. nov. Grey area and heavy line arcs show mouth cone and placids, respectively. The table lists the scalid arrangement by sector.
Fig. 6 in Echinoderes galadrielae Grzelak & Sørensen 2022, sp. nov.
Fig. 6. Echinoderes regina sp. nov., scanning electron micrographs. A, segments 1-3, laterodorsal view; B, introvert and segments 1-3, ventral view; C, segment 2, ventrolateral view; D, laterodorsal sensory spot on segment 1; E, segment 2, laterodorsal view; F, segment 4, dorsal view. Dashed circles indicate sensory spots. Abbreviations: gco2, type-2 glandular cell outlet; mds, middorsal acicular spine; ppf, primary pectinate fringe.
Fig. 7 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 7. Photographs of actual spawning of (a) S. spilurus and (b) L. bohar. Dotted yellow trace indicates a locus of a rushing female individual.
Fig. 6 in Echinoderes landersi Grzelak & Sørensen 2022, sp. nov.
Fig. 6. Nuptial coloration of: (a) S. spilurus and (b) L. bohar. Each male and female was marked M or F. Male were in the dark color morph, and female were in the light color morph.
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.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.