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163 results for “island biogeography”
FIGURE 1 in New species of Crotonia (Acari: Oribatida: Crotoniidae) from Lord Howe and Norfolk Islands: further evidence of long-distance dispersal events in the biogeography of a genus of Gondwanan relict oribatid mites
FIGURE 1. Crotonia gorgonia sp. nov. dorsal a) holotype female; b) paratype male.
FIGURE 5 in New species of Crotonia (Acari: Oribatida: Crotoniidae) from Lord Howe and Norfolk Islands: further evidence of long-distance dispersal events in the biogeography of a genus of Gondwanan relict oribatid mites
FIGURE 5. Crotonia utricularia sp. nov. holotype female a) dorsal; b) ventral.
FIGURE 2 in New species of Crotonia (Acari: Oribatida: Crotoniidae) from Lord Howe and Norfolk Islands: further evidence of long-distance dispersal events in the biogeography of a genus of Gondwanan relict oribatid mites
FIGURE 2. Crotonia gorgonia sp. nov. ventral a) holotype female; b) paratype male.
FIGURE 26 in A detailed description of Simulium (Meilloniellum) adersi (Pomeroy) from Mayotte, Comoro islands, with comments on bionomics and biogeography (Diptera: Simuliidae)
FIGURE 26. Simulium (Meilloniellum) adersi. Pupal abdominal armature. Structures not to scale.
FIGURE 1 in Inocellia rara sp. nov. (Raphidioptera: Inocelliidae), a new snakefly species from Taiwan, with remarks on systematics and biogeography of the Inocelliidae of the island
FIGURE 1. Habitus images of Inocellia rara sp. nov., holotype male. Scale bar = 1.0 mm.
Island biogeography theory and the urban landscape: stopover site selection by the silver-haired bat (Lasionycteris noctivagans)
<p>Many migratory bats require forested sites for roosting and foraging along their migration path, but increased urbanization and intensive agricultural practices may reduce the availability of stopover sites. Urban forests may provide important stopover habitat, maintaining landscape connectivity in regions where the majority of natural habitat has been cleared for development. Island biogeography theory can be applied to urbanized temperate forest biomes where small urban forests represent islands separated from the larger "mainland" forest. We used acoustic monitoring during the fall migration period to investigate the use of urban forest habitat by the migratory species <i>Lasionycteris noctivagans</i> (Le Conte 1831)<i>.</i> We predicted that recorded activity would have a positive relationship with forest patch area and shape and a negative relationship with isolation from other forest patches, as suggested by island biogeography theory. We observed greater activity at larger forest patches, and although relationships for shape and isolation were not statistically supported the observed patterns were consistent with predictions. Our results demonstrate the need for more in-depth research on the habitat requirements for both migratory and resident bat species and the impact that ongoing urbanization has on local bat populations.</p>
Data from: Do endemic mushrooms on oceanic islands and archipelagos support the theory of island biogeography?
<p class="MsoNormal">Terrestrial plant species on islands have a long history of study to determine how they evolved and what explains their levels of endemicity, but studies on fungi are lacking. Here, we examine: 1) how percent endemism of non-lichenized class Agaricomycetes; hereafter, "mushrooms" compares to angiosperms, ferns, bryophytes, and lichens from oceanic islands/archipelagos; 2) whether endemic mushrooms evolved from an ancestor diversifying into multiple species after island colonization (cladogenesis) or over time evolved into a single endemic species unique from its ancestral mainland counterpart (anagenesis); and 3) if mushroom percent endemism and cladogenesis are correlated to geographic variables that help explain these phenomena in other <span>species </span>groups.</p> <p class="MsoNormal">Checklists of mushrooms and other species groups from seven oceanic islands/archipelagos were compared. Having multiple endemic congeners from a single island/archipelago was used to infer cladogenesis versus anagenesis in endemic mushrooms. Pearson's correlation coefficients were calculated between an island/archipelago's percent endemism and percent cladogenesis, and their distance to the nearest mainland, area, maximum elevation, and latitude from the equator.</p> <p>These data contain information on mushrooms, angiosperms, ferns, bryophytes, and lichens from the Hawaiian Islands, Galápagos, Canary Islands, Madeira, Azores, Cabo Verde, and Christmas Island.</p>
Figure 4 in A new species of freshwater crab (Decapoda: Brachyura: Potamidae) from Dongyin Island, Matsu, Taiwan, defined by morphological and molecular characters, with notes on its biogeography
Figure 4. Neighbour-joining tree (Kimura two-parameter model) of Nanhaipotamon spp. and the outgroup Geothelphusa albogilva (GA) in this study based on 551 base pairs of the 16S rRNA gene. The bootstrap values (.50%) at the nodes represent confidence based on the percentage of 2000 bootstrap replications. For abbreviations of haplotypes see Table I.
Figure 3 in Biogeography, land snails and incomplete data sets: the case of three island groups in the Aegean Sea
Figure 3. Map of the island group of Kalymnos, with islands and sites studied.
Figure 1 in Biogeography, land snails and incomplete data sets: the case of three island groups in the Aegean Sea
Figure 1. Map of the island group of Skyros, with islands and sites studied.
Figure 11 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 11 - Continental paleogeography of the Late Cretaceous, highlighting the position of the European paleobioprovince (yellow dotted line). A Global paleogeography during the relative sea-level highstand period of the Turonian, showing maximum geographical fragmentation of Europe B Global paleogeography during the relative sea-level lowstand period of the latest Maastrichtian, showing significant extension of emergent areas. Abbreviations: AFR Africa; ANT Antarctica; APP Appalachia; AUS Australia; CAS Central (or Middle) Asia; EAS Eastern Asia; EUR Europe; IN India; IN-M Indo-Malagasy Landmass; LAR Laramidia; MA Madagascar; NAM North America; SAM South America; WAF western Africa. Base maps courtesy of R. Blakey.
Figure 12 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 12 - Diversity of Late Cretaceous European titanosaurs, as illustrated by posterior dorsal vertebral size and morphology (all specimens figured in right lateral view, unless specified otherwise). A Atsinganosaurus velauciensis (VBN 93.01), late Campanian, Velaux-La Bastide Neuve, Bouches-de-Rhône, southern France B Ampelosaurus atacis (MDE C3-247), late Campanian–early Maastrichtian, Bellevue, Aude, southern France C Lirainosaurus astibiae (MCNA 7443), late Campanian–early Maastrichtian, Laño, Basque Country, northern Spain D Magyarosaurus dacus (NHMUK R.4896, reversed), Maastrichtian, Sânpetru, Haţeg Basin, Romania E Paludititan nalatzensis (UBB NVM1-43), Maastrichtian, Haţeg Basin, Romania. Scale bars equal 10 cm in A–C and E and 5 cm in D. Photographs A–D courtesy by Verónica Díez Díaz.
Figure 7 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 7 - Representative taxa from the late Campanian–early Maastrichtian faunas from southern France. A Arcovenator escotae (Theropoda, Abelisauridae), braincase (MHNAix-PV 2011-12) in dorsal view (Lower Argiles Rutilantes Formation, Jas Neuf Sud, Var) B Rhabdodon priscus (Ornithopoda, Rhabdodontidae), left dentary (MC Mn 227) in lingual view (Grès à Reptiles Formation, Montplo Nord, Hérault) C Variraptor mechinorum (Theropoda, Dromaeosauridae), sacrum (MC PSP 6) in right lateral view (Grès à Reptiles Formation, Plo Saint-Pons, Hérault) D Martinavis cruzyensis (Aves, Enantiornithes), right humerus (MC M 1957) in caudal view (Grès à Reptiles Formation, Massecaps, Hérault) E Indeterminate titanosaur (Sauropoda, Titanosauria), caudal vertebra (MC M 0001) in left lateral view (Grès à Reptiles Formation, Massecaps, Hérault) F Struthiosaurus sp. (Ankylosauria, Nodosauridae), right scapulocoracoid (MC Mn 393) in lateral view (Grès à Reptiles Formation, Montplo Nord, Hérault) G Gargantuavis philoinos (Aves incertae sedis), synsacrum and part of ilia (MDE C3-525) in ventral view (Marnes de la Maurine Formation, Bellevue, Aude). All scale bars equal 50 mm.
Figure 3 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 3 - Paleogeographic distribution of the late Late Cretaceous (Santonian–Maastrichtian) European continental vertebrate assemblages (base map for late Campanian, ~ 75 Mya, courtesy of R. Blakey). Abbreviations: 1 Scania (southern Sweden) 2 Belgium-The Netherlands 3 western France 4 western Iberia (Portugal) 5 Cantabrian-southern Pyrenean region (northern Spain) 6 central Iberian region (central Spain) 7 eastern Iberian region (eastern Spain) 8 Languedoc (western southern France) 9 Provence (eastern southern France) 10 Apulia (southern Italy) 11 Adriatic-Dinaric Carbonate Platform (eastern Italy, Slovenia) 12 Austroalpine region (eastern Austria, western Hungary) 13 Transylvania (northwestern Romania) 14 northern Bulgaria 15 southeastern Poland 16 Crimea 17 southern Russia (for details, see also Figs 1, 4 and text); AA Austroalpine Domain; APP Appalachia; ARM Armorican Massif; BA-RHO Balkans-Rhodope Orogen; BAL Baltic Landmass; GRO Greenland; IB Iberian Landmass; MOE Moesian Platform; PEL Pelagonian Domain; PON Pontides Orogen; PY-PRO L Pyrenean-Provencal Landmass; RH-BH H Rhenish-Bohemian High; TAU Taurus Block; TI-DA Tisia-Dacia Block; UM-VH Ukrainian Massif-Voronezh High. Note that emergent land was more extensive during Maastrichtian times than represented in the map, with most Spanish-French localities situated in purely continental setting (compare with Fig. 11).
Figure 10 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 10 - Representative taxa from the latest Campanian–Maastrichtian faunas from Transylvania, western Romania. A–B Nidophis insularis (Serpentes, Madtsoiidae), articulated vertebrae (LPB (FGGUB) v.547/2) in left lateral (A) and dorsal (B) views (Densuş-Ciula Formation, Tuştea, Haţeg Basin; photo by Ştefan Vasile) C Allodaposuchus precedens (Eusuchia, ?Hylaeochampsidae), skull (PSMUBB V 438) in dorsal view (Sebeş = Şard Formation, Oarda de Jos, southwestern Transylvanian Basin; photo by Vlad Codrea/Massimo Delfino) D Theriosuchus sympiestodon (Mesoeucrocodylia, Atoposauridae), right maxilla (MCDRD 793) in lateral view (Sînpetru Formation, Sînpetru, Haţeg Basin) E–F Indeterminate titanosaur (?Magyarosaurus dacus) (Sauropoda, Titanosauria), isolated osteoderm (LPB (FGGUB) R.1410) in dorsal (E) and lateral (F) views (Sînpetru Formation, Sînpetru, Haţeg Basin) G Indeterminate ornithuran bird (Aves, Ornithurae), incomplete left tibiotarsus (LPB (FGGUB) R.1902) in anterior view (Densuş-Ciula Formation, Vălioara, Haţeg Basin) H Balaur bondoc (Theropoda, Dromaeosauridae), articulated left distal hindlimb (EME PV.313) in lateral view (Sebeş = Şard Formation, Sebeş-Glod, southewestern Transylvanian Basin; photo by Mick Ellison) I Zalmoxes robustus (Ornithopoda, Rhabdodontidae), right dentary (NHMUK R.3407) in medial view (Sînpetru Formation, Sînpetru, Haţeg Basin) J Telmatosaurus transsylvanicus (Hadrosauria), right maxilla (MFGI unnumbered) in lateral view (Sînpetru Formation, Sînpetru, Haţeg Basin) K Indeterminate nodosaurid – Struthiosaurus transylvanicus or new taxon – (Ankylosauria, Nodosauridae), isolated tooth (LPB (FGGUB) R.2182) in medial view (Sînpetru Formation, Sînpetru, Haţeg Basin) L Barbatodon transylvanicus (Multituberculata, Kogaionidae), right maxilla (LPB (FGGUB) M.1635) in medial view (Sînpetru Formation, Pui, Haţeg Basin). Scale bars equal 1 mm in A, B; 5 mm in K; 1 cm in G, L; 2 cm in D; and 5 cm in C, E, F, H, I, J.
Figure 9 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 9 - Representative taxa from the late Maastrichtian faunas from Spain. A Allodaposuchus subjuniperus (Crocodyliformes, Eusuchia), skull (holotype, MPZ 2012/288) in dorsal view (lower Tremp Formation, Beranuy near Arén, Huesca) B Arenysuchus gascabadiolorum (Crocodyliformes, Eusuchia), skull (holotype, MPZ ELI-1) in dorsal view (lower Tremp Formation, Arén, Huesca) C Indeterminate azhdarchid (Pterosauria, Azhdarchidae), cervical vertebra (MGUV 2271) in posterior view (unnamed unit (Margas de los Cuchillos Formation?), La Solana near Tous, Valencia). D–E Arenysaurus ardevoli (Ornithopoda, Lambeosaurinae) D partial skull (holotype, MPZ 2008/1) in dorsal view and E left dentary (paratype, MPS 2008/258) in medial view (basal Tremp Formation, Blasi 3, Arén, Huesca) F 'Koutalisaurus kohlerorum' (Ornithopoda, Lambeosaurinae; indeterminate lambeosaurine sensu Prieto-Márquez et al. 2013), right dentary (IPS 29920 (formerly IPS SRA 27) in medial view ('lower red unit' of the Tremp Formation, Les Llaus near Sant Romà d'Abella, Lleida) F Scale bars equal 10 cm (A–B, D–F), and 5 cm (C). Photographs courtesy by Museo de Ciencias Naturales de la Universidad de Zaragoza (A–B, D), Julio Company (C) and Alberto Prieto-Márquez (E–F).
Figure 2 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 2 - Paleogeographic distribution of the early Late Cretaceous (Cenomanian–Coniacian) European continental vertebrate assemblages (base map for earliest Cenomanian, ~ 100 Mya, courtesy of R. Blakey). Abbreviations: 1 southeastern England 2 western France 3 southern France 4 western Iberia (Portugal) 5 northern Iberia (northern Spain) 6 east-central Iberia (eastern Spain) 7 Apulia (Sicily, central Italy) 8 Adriatic-Dinaric Carbonate Platform (Croatia, Slovenia) 9 Czech Republic 10 northwestern Romania 11 southern Russia (for details, see also Fig. 1 and text); AA Austroalpine Domain; ARM-FMC Armorica-French Central Massif; BAL Baltic Landmass; BM Bohemian Massif; DAC Dacia Block; GRO Greenland; LAU Laurentian Shield; L-B H London-Brabant High; MOE Moesian Platform; PEL Pelagonian Domain; TAU Taurus Block; TIS Tisia Block; UM Ukrainian Massif; VH Voronezh High.
Figure 8 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 8 - Representative taxa from the late Campanian–early Maastrichtian faunas from Spain. A Iberoccitanemys convenarum (Pleurodira, Bothremydidae), complete shell (HUE-4913) in ventral view (Villalba de la Sierra Formation, Lo Hueco near Fuentes, Cuenca) B Dortoka vasconica (Pleurodira, Dortokidae), partial shell (holotype, MCNA 6313) in ventral view (unnamed unit, Laño, Condado de Treviño) C Menarana laurasiae (Serpentes, Madtsoiidae), mid-trunk vertebra (holotype, MCNA 5337) in posterior view (unnamed unit, Laño, Condado de Treviño) D Herensugea caristiorum (Serpentes, Madtsoiidae), mid-trunk vertebra (holotype, MCNA 5387) in dorsal view (unnamed unit, Laño, Condado de Treviño) E Rhabdodon sp. (Ornithopoda, Rhabdodontidae), maxillary tooth (MGUV CH-162) in labial view (Sierra Perenchiza Formation, Chera, Valencia) F Struthiosaurus sp. (Ankylosauria, Nodosauridae), synsacrum (MCNA 7420.1) in ventral view (unnamed unit, Laño, Condado de Treviño) G Ampelosaurus sp. (Sauropoda, Titanosauria), braincase (HUE-8741) in dorsal view (Villalba de la Sierra Formation, Lo Hueco near Fuentes, Cuenca) H Doratodon ibericus (Crocodyliformes, Ziphosuchia), left dentary (holotype, MGUV 3201) in lateral view (Sierra Perenchiza Formation, Chera, Valencia) I Musturzabalsuchus buffetauti (Crocodyliformes, Eusuchia), right mandible (paratype, MCNA 7480) in lateral view (unnamed unit, Laño, Condado de Treviño) J Lainodon orueetxebarriai (Eutheria, Zhelestidae), first lower molar (holotype, MCNA L1AT 14) in occlusal and labial views (unnamed unit, Laño, Condado de Treviño). Scale bars equal 10 cm (A, F, I), 5 cm (B, G), 2 cm (H), 1 cm (C, E), 5 mm (D), 1 mm (J). Photographs courtesy by Adán Pérez-García (A), J. Carmelo Corral (B–D), Julio Company (E, H), GBE-UNED/MCCM (G), Francisco Ortega (I) and Emmanuel Gheerbrant (J).
Figure 1 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 1 - Late Cretaceous vertebrate localities from Europe (including European part of Russia), plotted and listed by age (see text for details and references; localities italicized are detailed in Fig. 4 and in the text, as indicated). Note that one data-point on the map can represent several fossil localities and sites, especially for the Campanian and Maastrichtian. Cenomanian: 1 Isle of Wight, southeastern UK 2 Cambridgeshire, southeastern UK 3 Kent, southeastern UK 4 Sarthe, western France 5 Maine-et-Loire, western France 6 Vienne, western France 7 Indre-et-Loire, western France 8 Dordogne, western France 9 Vaucluse, southern France 10 Gard, southern France 11 Charente-Maritime, Charente, western France 12 Carenque, southwestern Portugal 13 Asturias, northern Spain 14 Guadalajara, central Spain 15 Teruel, central-eastern Spain 16 Valencia, eastern Spain 17 Sicily, Italy 18 Lazio, central Italy 19 Istria, Croatia 20 Czech Republic 21 Kursk Oblast, Russia 22 Belgorod Oblast, Russia 23 Voronezh Oblast, Russia 24 Tambov Oblast, Russia 25 Saratov Oblast, Russia 26 Volgograd Oblast, Russia. Turonian: 27 East Sussex, southeastern UK 28 Vendée, western France 29 Asturias, northern Spain 30 Czech Republic 31 Istria, Croatia 32 Dalmatia, Croatia. Coniacian: 33 Kent, southeastern UK 34 Gorizia, northeastern Italy 35 Bihor, western Romania (see section F, Fig. 4). Santonian: 36 Valencia, eastern Spain 37 Vendée, western France 38 Lonzée, central Belgium 39 Kras, Slovenia 40 Bari, southern Italy 41 Iharkút, western Hungary (see section B, Fig. 4). Campanian: 42 Scania, southern Sweden 43 Villeveyrac, Languedoc, southern France (see section D, Fig. 4) 44 Muthmannsdorf, eastern Austria (see section C, Fig. 4) 45 northwestern Transylvania, Romania (see section F, Fig. 4) 46 Penza Oblast, Russia 47 Saratov Oblast, Russia 48 Volgograd Oblast, Russia. Late Campanian–Maastrichtian: 49 Aveiro-Coimbra districts, Portugal 50 Condado de Treviño, northern Spain 51 Segovia, central Spain 52 Cuenca, central Spain 53 Valencia, eastern Spain 54 Huesca, northeastern Spain 55 Lleida, northeastern Spain (for 49–55 see section E, Fig. 4) 56 Ariège and Aude, southern France 57 Hérault and Gard, southern France 58 Bouches-du-Rhône, southern France 59 Var, southeastern France (for 56–59 see section D, Fig. 2) 60 Trieste, northeastern Italy. Maastrichtian: 61 Limburg, northeastern Belgium, southeastern Netherlands 62 Burgos, northern Spain 63 Valencia, eastern Spain 64 Huesca, northeastern Spain 65 Lleida, northeastern Spain (for 62–65 see section E, Fig. 4) 66 Haute-Garonne, Aude, southern France 67 Bouches-du-Rhône, southern France (for 66–67 see section D, Fig. 4) 68 Bavaria, southern Germany 69 Kras, Slovenia 70 northwestern Transylvanian Basin, Romania 71 southwestern Transylvania, Romania 72 Hațeg and Rusca Montană Basins, Romania (for 70–72 see section F, Fig. 4) 73 Vratsa Province, northwestern Bulgaria 74 Roztocze, southeastern Poland 75 Krymskaya Oblast, Ukraine 76 Volgograd Oblast, Russia.
Figure 6 from: Csiki-Sava Z, Buffetaut E, Ősi A, Pereda-Suberbiola X, Brusatte SL (2015) Island life in the Cretaceous - faunal composition, biogeography, evolution, and extinction of land-living vertebrates on the Late Cretaceous European archipelago. ZooKeys 469: 1-161. https://doi.org/10.3897/zookeys.469.8439
Figure 6 - Representative taxa from the early Campanian Muthmannsdorf fauna from the Grünbach Formation, eastern Austria. A Doratodon carcharidens (Mesoeucrocodylia) mandible (PIUW 2349/57) in dorsal view (photo by Márton Rabi) B Indeterminate azhdarchid (Pterosauria, Azhdarchidae), left humerus (PIUW 2349/102) in anterior view C 'Megalosaurus pannoniensis' basal tetanuran (Theropoda, Tetanurae), tooth (PIUW uncatalogued) in lateral view D Mochlodon suessi (Ornithopoda, Rhabdodontidae), right dentary (holotype, PIUW 2349/2) in medial view. Scale bars equal 2 cm in A, B and D and 1 cm in C.
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