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183 results for “mediterranean islands”
Figure 18 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 18. Anatomy of Pseudamnicola (Pseudamnicola) gasulli from a stream at Barranco de las Negras, Almería, Spain. A, B, partial nervous system. C, ctenidium and osphradium. D, prostate gland. E, stomach. F, head and penis of a male. G, female genitalia. H, bursa copulatrix.
Figure 13 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 13. Shells of Pseudamnicola (Pseudamnicola) subproducta. A, D, shells from Baltasar Ullal, Tarragona, Spain. B, shell from Font Estramar, Perpignan, France. C, shell from Ontígola Lagoon, Madrid, Spain. E, F, H, protoconch and microsculpture of shell from Baltasar Ullal, Tarragona, Spain. G, microsculpture of shell from Ontígola Lagoon, Madrid, Spain.
Figure 12 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 12. Anatomy of Pseudamnicola (Pseudamnicola) meloussensis from a stream at Macarella Creek, Minorca. A, B, partial nervous system. C, ctenidium and osphradium. D, prostate gland. E, stomach. F, head and penis of a male. G, female genitalia. H, bursa copulatrix and seminal receptacle.
Figure 2 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 2. Phylogenetic relationships of the Ibero-Balearic Pseudamnicola (Pseudamnicola) species based on the Bayesian topology recovered from the combined data set of mitochondrial (cytochrome c oxidase subunit I and 16S rRNA) and nuclear (28S rRNA) fragments. The '?' and colouring of Ibiza Island represent the fact that although populations of Pseudamnicola (Pseudamnicola) gasulli from Ibiza were not found in our study, it has been previously cited for this location. For locality codes, see Table 1. Branch supports are given above species level as follows: ** represents bootstrap support values ≥ 95% and posterior probabilities ≥ 0.95 and * indicates bootstrap support values of maximum parsimony ≥ 95%, maximum likelihood between 50 and 75% and posterior probabilities ≥ 0.95. (Colour figure available online.)
Figure 5 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 5. Protoconch details of Majorcan species. A, B, Pseudamnicola (Pseudamnicola) beckmanni from El Rentador Spring, Deyá. C, D, Pseudamnicola (Pseudamnicola) granjaensis from La Granja, Esporles. E, F, Pseudamnicola (Pseudamnicola) artanensis from a ditch near Betlem Hermitage, Artá. Arrows point to the edge of protoconch.
Figure 6 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 6. Inner side (left column) and outer side (right column) of the operculum of the following species: A, B, Pseudamnicola (Pseudamnicola) beckmanni from El Rentador Spring, Deyá, Majorca. C, D, Pseudamnicola (Pseudamnicola) granjaensis from La Granja, Esporles, Majorca. E, F, Pseudamnicola (Pseudamnicola) artanensis from a ditch near Betlem Hermitage, Artá, Majorca.
Figure 10 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 10. Shells of Pseudamnicola (Pseudamnicola) meloussensis from a stream at Macarella Creek, Minorca. A–D, frontal and lateral views of the observed morphotypes. E–G, protoconch and details of protoconch microsculpture. Scale bar: 1 mm.
Figure 8 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 8. Prostate gland (first row), head and penis of a male (second row), female genitalia with details of the bursa copulatrix and seminal receptacle (third row), and nervous system (fourth row) of the Majorcan species: A, D, G, J, Pseudamnicola (Pseudamnicola) beckmanni from El Rentador Spring, Deyá. B, E, H, K, Pseudamnicola (Pseudamnicola) granjaensis from La Granja, Esporles. C, F, I, L, Pseudamnicola (Pseudamnicola) artanensis from a ditch near Betlem Hermitage, Artá. Scale bar: 1 mm.
Figure 7 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 7. General view of radula (first row), rows of teeth of the radula (second row), central teeth (third row), and detail of outer marginal teeth (fourth row) of the Majorcan species: A, D, G, J, Pseudamnicola (Pseudamnicola) beckmanni from El Rentador Spring, Deyá. B, E, H, K, Pseudamnicola (Pseudamnicola) granjaensis from La Granja, Esporles. C, F, I, L, Pseudamnicola (Pseudamnicola) artanensis from a ditch near Betlem Hermitage, Artá.
Figure 9 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 9. Ctenidium, osphradium, and rectum (first row) and stomach (second row) of the Majorcan species: A, D, Pseudamnicola (Pseudamnicola) beckmanni from El Rentador Spring, Deyá. B, E, Pseudamnicola (Pseudamnicola) granjaensis from La Granja, Esporles. C, F, Pseudamnicola (Pseudamnicola) artanensis from a ditch near Betlem Hermitage, Artá.
Figure 4 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 4. Front, lateral, and apical views of shells of Majorcan species. A, D, G, shells of Pseudamnicola (Pseudamnicola) beckmanni from El Rentador Spring, Deyá. B, E, H, shells of Pseudamnicola (Pseudamnicola) granjaensis from La Granja, Esporles. C, F, I, shells of Pseudamnicola (Pseudamnicola) artanensis collected from a ditch near Betlem Hermitage, Artá. Scale bar: 1 mm.
Figure 3 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 3. *BEAST chronograms of Pseudamnicola (Pseudamnicola) populations from the Ibero-Balearic region based on different calibrations: A, combined analysis of cytochrome c oxidase subunit I (rate previously calibrated for hydrobiids) and 16S rRNA and 28S rRNA ribosomal fragments (rates estimated), B, combined analysis in which all the rates and ages were estimated by a geological event (the separation of Minorca Island from the continent). *BEAST posterior probabilities were 0.99, except for the one indicated with a black dot, which was 0.75. Grey bars indicate 95% highest posterior density intervals. Black arrows on branches indicate no constancy in evolutionary rates using the relative rate test.
Figure 1 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 1. Distribution map of Pseudamnicola (Pseudamnicola) populations in the Ibero-Balearic region that were molecularly examined. For locality codes, see Table 1.
Figure 17 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 17. Operculum and radula of Pseudamnicola (Pseudamnicola) gasulli from Retamar Rambla, Almería (operculum) and stream at Barranco de las Negras, Almería (radula). A, internal side of the operculum. B, external side of the operculum. C, radula. D, rows of teeth of the radula. E, central teeth. F, outer marginal teeth.
Figure 15 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 15. Anatomy of Pseudamnicola (Pseudamnicola) subproducta from Baltasar Ullal, Tarragona, Spain. A, B, partial nervous system. C, ctenidium and osphradium. D, prostate gland. E, stomach. F, head and penis of a male. G, female genitalia. H, bursa copulatrix and seminal receptacle.
Figure 16 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 16. Shells of Pseudamnicola (Pseudamnicola) gasulli. A, shell from a stream at Barranco de las Negras, Almería, Spain. B, shell from Retamar Rambla, Almería, Spain. C–G, shells from a stream at Rambla de los Yesos, Alboloduy, Spain. E–G, protoconch and microsculpture of the protoconch. Scale bar: 1 mm.
Figure 14 in Vicariant versus dispersal processes in the settlement of Pseudamnicola (Caenogastropoda, Hydrobiidae) in the Mediterranean Balearic Islands
Figure 14. Operculum and radula of Pseudamnicola (Pseudamnicola) subproducta from Baltasar Ullal, Tarragona, Spain. A, internal side of the operculum. B, external side of the operculum. C, radula. D, rows of teeth of the radula. E, central teeth. F, details of outer marginal teeth.
Figure 1 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 1. Diagram of Mediterranean Islands showing endemic genera and species of soricids from the Plio–Quaternary to the present: white shrew silhouettes, current species; grey shrew silhouettes, extinct or with presence in the fossil record. From west to east: species of Nesiotites (extinct) from the Gymnesic Islands; species of Asoriculus (extinct) from the Corso-Sardinian complex; Asoriculus burgioi (extinct) from Sicily; Crocidura sicula sicula (present in the fossil record and extant) and Crocidura sicula esuae (extinct) from the Sicilian–Maltese archipelago; Crocidura zimmermanni (present in the fossil record and extant) from Crete; and Crocidura suaveolens praecypria (extinct) from Cyprus. See text for references.
Figure 2 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 2. Chronological framework of the species used in the study: in black, species related to the tribe Nectogalini; in grey, Crocidura species. The circles highlight the species analysed from different sites sorted biochronologically (connected by a thick line), the squares highlight the species analysed from only one site, and the empty squares highlight the mainland (ancestor) species. Below the species: the site, locality, and molar/s used for estimating body mass are listed.
Figure 4 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 4. Estimations of body masses (in g) of Nesiotites species (row A, lower molars) and Crocidura zimmermanni (row B, lower molars; and row C, upper molars) from different sites ordered chronologically (see Table 2 for site acronyms). The first column shows the predictions of body mass using all of the estimators (white square, LM1; black circle, WM1; grey circle, TRLM1; grey square, AAM1; white circle, TRAAM1) and the following columns represent each measurement separately (LM1, WM1, TRLM1, AAM1, and TRAAM1, respectively). In order to observe the fluctuation of the points, we linked the points with a line. Dotted lines in Nesiotites diagrams (row A) separate the three statistically different subgroups.
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