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1,692 results for “Caenogastropoda”
Figure 25 in Shell features and anatomy of the springsnail genus Radomaniola (Caenogastropoda: Hydrobiidae) show a different pace and mode of evolution over five million years
Figure 25. Anatomy of Radomaniola wolffi sp. nov. A–H, paratypes (UGSB 19533). A, ctenidium and osphradium. B, stomach. C, partial nervous system. D, pallial oviduct. E, bursa copulatrix and seminal receptacles. F, head of male and penis. G, penis. H, prostate gland.
Figure 18 in Shell features and anatomy of the springsnail genus Radomaniola (Caenogastropoda: Hydrobiidae) show a different pace and mode of evolution over five million years
Figure 18. Shells, operculum and radulae of Radomaniola pesici sp. nov. A, B, holotype (MNCN 15.05/200163). C–J, paratypes (UGSB 19048). C, D, shells. E, F, operculum (E, inner side; F, outer side). G, protoconch. H, portion of radula ribbon. I, central radular teeth. J, outer marginal teeth.
Figure 23 in Shell features and anatomy of the springsnail genus Radomaniola (Caenogastropoda: Hydrobiidae) show a different pace and mode of evolution over five million years
Figure 23. Anatomy of Radomaniola variabilis sp. nov. A–G, I, paratypes (UGSB 23975). H, J, UGSB 14440. K, UGSB 2294. A, ctenidium and osphradium. B, stomach. C, partial nervous system. D, pallial oviduct. E, bursa copulatrix and seminal receptacles. F, prostate gland. G, H, head of male and penis. I–K, penis.
FIGURE 1 in A Georgian and an Iranian new species of Renea G. Nevill, 1880 enormously extend the genus's distribution (Gastropoda: Caenogastropoda: Aciculidae)
FIGURE 1. Extant (darker grey) and fossil (lighter grey) distribution of the genus Renea G. Nevill, 1880 (after Boeters et al. 1989 and Lika et al. 2021), and type localities of the new species. Triangle: Renea caucasica n. sp., circle: Renea nemethi n. sp.
Supplementary material 2 from: Hershler R, Liu H-P, Hubbart N (2017) Two new species of Fluminicola (Caenogastropoda, Lithoglyphidae) from southwest Oregon, USA, and a range extension for F. multifarius. ZooKeys 679: 1-20. https://doi.org/10.3897/zookeys.679.13472
Distribution of COI haplotypes : Explanation note: Exemplars used in the phylogenetic analyses are in parentheses.
Supplementary material 3 from: Hershler R, Liu H-P, Hubbart N (2017) Two new species of Fluminicola (Caenogastropoda, Lithoglyphidae) from southwest Oregon, USA, and a range extension for F. multifarius. ZooKeys 679: 1-20. https://doi.org/10.3897/zookeys.679.13472
Distribution of cytB haplotypes : Explanation note: Exemplars used in the phylogenetic analyses are in parentheses.
Supplementary material 1 from: Hershler R, Liu H-P, Hubbart N (2017) Two new species of Fluminicola (Caenogastropoda, Lithoglyphidae) from southwest Oregon, USA, and a range extension for F. multifarius. ZooKeys 679: 1-20. https://doi.org/10.3897/zookeys.679.13472
Sample codes, locality details (voucher numbers for newly sequenced specimens in parentheses), and GenBank accession numbers for COI and cytB sequences :
Supplementary material 2 from: Hershler R, Liu H-P, Babbitt C, Kellogg MG, Howard JK (2016) Three new species of western California springsnails previously confused with Pyrgulopsis stearnsiana (Caenogastropoda, Hydrobiidae). ZooKeys 601: 1-19. https://doi.org/10.3897/zookeys.601.9040
Specimens of Pyrgulopsis stearnsiana sensu stricto that were examined as part of this study : Explanation note: All material is from California.
FIGURE 1. Severnsia strombeulima n in Severnsia strombeulima n. gen. & sp. from Hawaii (Mollusca, Gastropoda: Caenogastropoda: Eulimidae)
FIGURE 1. Severnsia strombeulima n. gen. & sp. Off Maui, Hawaii, USA, 20° 39.290′N, 156° 29.561′W, 433–407 ft [= 144–136 m]. A. Holotype. SBMNH 454737. 1.57 mm B. Paratype SBMNH 457572. 1.67 mm. * indicates the downturn of the flared apertural lip.
Supplementary material 1 from: Boulaassafer K, Ghamizi M, Delicado D (2018) The genus Mercuria Boeters, 1971 in Morocco: first molecular phylogeny of the genus and description of two new species (Caenogastropoda, Truncatelloidea, Hydrobiidae). ZooKeys 782: 95-128. https://doi.org/10.3897/zookeys.782.26797
Table 1–6 : Explanation note: Measurements recorded for the shell, radula, ctenidium, osphradium, digestive system, female and male genitalia, and nervous system in the Mercuria species examined.
FIGURES 35–42 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURES 35–42. Protoconch and teleoconch sculpture in Paladilhiopsis cf. bosniaca. 35–36. Shell. 37–38. Protoconch. 39. Protoconch and teleoconch sculpture. 40. Outer surface of the body whorl (teleoconch), with ribs and spiral riblets (striae). Scale bar = 500 µm in figs 35–36; 125 µm in fig. 37;50 µm in fig. 38; 250 µm in fig. 39 and 25 µm in figs 40–42.
FIGURE 60 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURE 60. The COI-based maximum-likelihood relationships. Bootstrap support (>65 %) and Bayesian posterior probabilities (>0.95) are shown. The generic assignments are molecularly based, the generic assignments used so far are given in green. The Moitessieriidae are on the sand background.
FIGURES 23–34 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURES 23–34. Shells of Paladilhiopsis, Iglica and Bythiospeum. 23–25. Paladilhiopsis grobbeni Kuščer, 1928, Raja peč, type locality; ZMUJ2121–ZMUJ2122. 26–28. I. gittenbergeri A. Reischutz & P.L. Reischutz, 2008, Albania; ZMUJ2130–ZMUJ2132. 29–31. Paladilhiopsis bosniaca (Clessin, 1910), source Handek, Šumeće, Travnik, Bosnia and Herzegovina; ZMUJ2126–ZMUJ2127, ZMUJ2212. 32. I. cf. absoloni (A.J. Wagner, 1914), source Vrelo, Gradište, Pirot, Serbia; ZMUJ2129. 33. B. blihensis Glöer et Grego, 2015, Donji Kamengrad, Bosnia and Herzegovina; ZMUJ2123. 34. B. maroskoi Glöer et Grego, 2015, Gornja Pecka, Bosnia and Herzegovina; ZMUJ2125. Scale bar = 1 mm.
FIGURE 62 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURE 62. The portion of Figure 60, based on COI sequences, showing only Moitessieriidae with Cochliopidae, with morphological character states given. Molecular-based species names are used. Schematic drawings are original or based on Giusti (1975), Glöer (2002), Girardi (2009), Niero & Pezzoli (2016).
FIGURES 2–22 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURES 2–22. Shells of Iglica, Costellina, Lanzaia and Moitessieria. 2–6. Iglica cf. forumjuliana (Pollonera, 1887), cave Matešića pećina, Matešići, Slunj, Croatia; ZMUJ2114– ZMUJ2115, ZMUJ2202–ZMUJ2204. 7–10. I. cf. hauffeni (Brusina, 1886), Babja luknja near Goričane, Slovenia; ZMUJ2105–ZMUJ2106, ZMUJ2205–ZMUJ2206. 11–12. I. cf. gracilis (Clessin, 1882), Slovenia. 11. Obrežje, river Sava; ZMUJ2110. 12. Terme Čatež, Čatež ob Savi, river Sava; ZMUJ2108. 13–14. Iglica hellenica Falniowski et Sarbu, 2015, Melissotrypa Cave, Thessalia, Greece: 13. Holotype MZUJ2107. 14. Paratype, MZUJ2209, destroyed for DNA extraction. 15–18. Costellina turrita Kuščer, 1933, spring of river Jadro, Solin, Split, type locality: 15. MZUJ2128. 16. MZUJ2211. 17–18. Teloconch sculpture. 19–20. Lanzaia bosnica Bole, 1970, young specimens, Dabarska Pećina, Dabar, Bosnia and Herzegovina; ZMUJ2124. 21–22. Moitessieria sp., gravel bar, river Arga, Akerreta, Pamplona, Spain; ZMUJ2116–21117. Scale bar 1 mm for the shells, 200 µm for fig. 17 and 100 µm for fig. 18.
FIGURE 1 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURE 1. Sampling localities as in Table 1. Molecular-based members of the genera Iglica marked in red, Paladilhiopsis in blue, Moitessieria in black.
FIGURE 61 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURE 61. The maximum-likelihood tree of the all four concatenated genes. Bootstrap support (>65 %) and Bayesian posterior probabilities (>0.95) are shown. Molecular-based, as well as used so far (in green) species names and genus assignments are given.
FIGURE 59 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURE 59. The maximum-likelihood trees of three nuclear genes (18S, 28S and H3) and their concatenated three. Bootstrap support (>65 %) and Bayesian posterior probabilities (>0.95) are shown. Molecular-based, including (in green) species names used in the text and generic assignments.
FIGURES 55–58. Reproductive organs. 55–56. Female reproductive organs. 55 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURES 55–58. Reproductive organs. 55–56. Female reproductive organs. 55. Iglica cf. forumjuljana. 56. Paladilhiopsis grobbeni (bc—bursa copulatrix, cbc—duct of bursa copulatrix, ga—albumen gland, gn—capsule gland, gp—gonopore, ov—oviduct, ovl—loop of oviduct, rs—seminal receptacle). 57–58. Penis. 57. Iglica cf. forumjuliana. 58. Paladilhiopsis grobbeni. Asterisks mark outgrowths. Scale bar = 0.5 mm.
FIGURES 43–54 in Phylogenetic relationships of the Balkan Moitessieriidae (Caenogastropoda: Truncatelloidea)
FIGURES 43–54. Protoconch and teleoconch sculpture in Iglica cf. hauffeni and Moitessieria sp. 43–46. I. cf. hauffeni. 43. Shell. 44. Protoconch. 45–46. Outer surface sculpture of the body whorl (teleoconch). 47–54. Moitessieria sp. 47. Outer surface sculpture of penultimate and body whorl (teleoconch). 48. Shell. 49–50. Protoconch. 51. Spiral sculpture close to the aperture. 52–54. Spiral sculpture of the penultimate and body whorl. Scale bar = 500 µm in figs 43, 48; 250 µm in fig. 47; 125 µm in figs 44, 50; 50 µm in figs 49, 51–53; and 25 µm in figs 45, 46, 54.
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