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Fig. 1 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 1. Measurement of MXR activity in Physa acuta snails according to seasons. (A) The accumulation of RB has been assessed in control snails and after inhibition with 30 μM verapamil. Data are expressed in picomoles of accumulated RB per gram of entire snail body weight. The symbol (*) indicates a significant difference compared to the other bars in control condition (p <0.05, n = 7). (B) Bars represent the R-value calculated from the data present in the panel A (control /verapamil). In all cases, bars represent standard deviation of the mean.
Fig. 1. A in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 1. A: map of southern South America indicating the collecting localities of the examined specimens of Microcavia. Ellipses shown the groupings of localities that constitute the geographical samples analyzed. See Materials and Methods for an explanation of the acronyms. Different symbols correspond to the three species identified in this work: white circles = M. australis; black circles = M. maenas; black squares = M. jayat n. sp. B. map of southern South America indicating the type localities of names associated with Microcavia australis.
Fig. 3 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 3. Representation of R -values as a parameter to determine the MXR activity in P. acuta snails versus water temperature. R -value negatively correlates with water temperature (Spearman rs = 0.48, p = 0.013; n = 26).
Fig. 5 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 5. Selected anatomical traits of three species of Microcavia (A, MACN-Ma 16379; B, MACN-Ma 34.81; C, MACN-Ma 17331; D, MACN-Ma 16379; E, MACN-Ma 36.72; F, MACN-Ma 17333; G, MACN-Ma 28.51; H, MACN-Ma 36.84; I, MACN-Ma 17331), depicting the relative position of inferior process of the jugal (marked by the arrow) relative to the glenoid cavity (a-c) and size and shape of the palatal cristae (d-i). A, D, G = M. australis; B, E, H = M. maenas; C, F, I = M. n. sp. Abbreviations: gc = glenoid cavity; jf = jugal fossa; mpp = medial process of the palate; pc = palatal crista; sq = squamosal. Photographs are not in scale to facilitate comparisons among proportions.
Fig. 4 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 4. Lateral views of the skull and right dentaries in labial views of three species of Microcavia: M. australis (A; MACN-Ma 14.543), M. maenas (B; MACN-Ma 34.116) and Microcavia n. sp. (C; MACN-Ma 17331). Scale bars = 5 mm.
Fig. 11 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 11. Left upper and lower left molar rows (A, B) of the holotype (MACN-Ma 17331) and (C, D) paratype (MACN-Ma 17333) of Microcavia jayat n. sp., from Santa Isabel, Santiago del Estero, Argentina (MACN-Ma 17331). Scale bars = 5 mm.
Fig. 3 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 3. (A) Water temperature in the four zones (I-IV) on the census route from November 2011 to June 2014. (B) Monthly average of the number of individuals per census of the five gastropterid species.
Fig. 7 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 7. Lateral view of the zygomatic arch in three species of Microcavia: M. australis (A; MACN-Ma 14.543), M. maenas (B; MACN-Ma 34.116) and Microcavia n. sp. (C; MACN-Ma 17333). Abbreviation: pp = paraorbitary process. Photographs are not in scale to facilitate comparisons among proportions.
Fig. 8 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 8. Specimen scores of adult individuals (ages 3-5) of Microcavia (N = 144) for: A) Principal components 1 and 2; B) Canonical variates 1 and 2, extracted from discriminant function analyses of 18 geographic groups; C) Between morphogroup principal components 1 and 2; D) Canonical variates 1 and 2, extracted from three-group discriminant function analysis. For the acronyms of the geographical samples see Materials and Methods section.
Fig. 2 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 2. In situ photographs of gastropterids at the study site with approximate scales. (A) Sagaminopteron ornatum. (B) Siphopteron brunneomarginatum. (C) Si. citrinum. (D) Si. flavum. (E) Si. tigrinum. Scale bars: A = 10 mm, B-E = 1 mm. © 2017 Academia Sinica, Taiwan
Fig. 10 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 10. Holotype of Microcavia jayat n. sp., from Santa Isabel, Santiago del Estero, Argentina (MACN-Ma 17331): skull in right lateral (above), dorsal (below, left) and ventral (below, right) views, and left dentary (reversed) in labial view. Scale bars = 5 mm.
Fig. 3 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 3. Relationship between percentage of pulp + seeds in the diets and maximum difference between seasonal litter percentages. Same legend as for figure 2.
Fig. 1 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 1. Rainfall (1981-1991; curve, in mm) and number of fruiting trees per km of trail (1980-1982; black bars) according to the month (from Gayot et al. 2004).
Fig. 2 in Zavreliella shidai Han & Liu & Luo & Tang 2021, sp. n.
Fig. 2. (a) Average monthly number of fruiting trees per km (continuous line) and average monthly rainfall (in mm; dashed line); (b) Percentage of litters over the yearly total, according to the season. Number of pregnant females -- 35, 30, 36, 35, 44, 29 -- and number of litters -- 58, 109, 9, 121, 35, 89 -- in H. megacephalus, P. cuvieri, M. acouchy, D. leporina, A. paca and T. tajacu, respectively. H. megacephalus (black squares), P. cuvieri (white squares), M. acouchy (black triangles), D. leporina (white triangles), A. paca (black diamonds), and T.tajacu (white diamonds). F-Ap: February-April; M-Jy: May-July; A-O: August-October; N-J: November-January.
Fig. 5 in Ophiomonas shinseimaruae Okanishi & Matsuo & Fujita 2021, sp. n.
Fig. 5. Boundary zones confirmed in the field. a, Most colonies of Montipora digitata were fragmented and covered by T. hoshinota in Ogimi, Japan. b, Enlarged view of a. Arrowheads indicate boundary zones between individuals. c, Distinct boundary zone (arrow heads) on a massive coral Porites in Ogimi. The insert is an enlarged view of the threads. Yellow patches are brown algae covering the dead coral surface. d, The boundary between two individuals (arrow heads) on foliose coral Montipora aequituberculata in Nakijin.
Fig. 3 in Ophiomonas shinseimaruae Okanishi & Matsuo & Fujita 2021, sp. n.
Fig. 3. Results of a, growing-edge contact assays and b, direct contact assays. Five replicated sets were examined for each pair. Individuals are from Nakijin (N1–N5, and N), Sesoko (S1–S2, and S), and Ogimi (O1–O4, and O). Assays between distant reefs are provided as N, O, and S.
Fig. 4 in Ophiomonas shinseimaruae Okanishi & Matsuo & Fujita 2021, sp. n.
Fig. 4. Vertical sections of the boundary zone stained with Picro-sirius red. a and b, Rejection reactions between two individuals. c and d, Fusion between two fragments of the same individual. a, Boundary formation between two individuals and a spicule stuck into another individual (arrowhead). b, Gathered mesohyl between two individuals (arrow). c, A collagenous structure (stained pink) formed at the contact interface. d, Fusion of the sponge tissue. Asterisks indicate the dermal-like layer to indicate the boundary region between two sponges.
Fig. 2. Contact experiments with Terpios hoshinota sponge. a in Ophiomonas shinseimaruae Okanishi & Matsuo & Fujita 2021, sp. n.
Fig. 2. Contact experiments with Terpios hoshinota sponge. a, Two fragments from different individuals (N1 × N2) in the direct contact assay (at day 0). b, Boundary zone (arrow heads) between two individuals (N4 × N5) in the growing-edge contact assay (at day 19). c, Enlarged view of b. d, Colony of Montipora coral (81 cm in diameter) which was covered by sponge patches of N4 and N5 in Nakijin.
Fig. 1 in Ophiomonas shinseimaruae Okanishi & Matsuo & Fujita 2021, sp. n.
Fig. 1. Map of the study sites (Sesoko, Nakijin, and Ogimi) in the northern area of Okinawa Island, Japan.
Fig. 2 in Striatoandricus sanchezi Cuesta-Porta & Melika & Nicholls & Stone & Pujade-Villar 2022, n. sp.
Fig. 2. Holotype of Somniosus (Rhinoscymnus) cheni sp. nov. (EBFSFSX001), pregnant female, 1340 mm total length. Photo by C. Y. Lin.
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International Brain Laboratory public data
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OpenNeuro
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