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122 results for “Paradoxa”
Echinacea paradoxa (Asteraceae) - leaf - on upper stem
Image of Echinacea paradoxa (Asteraceae) - leaf - on upper stem
Linked collectors and determiners for: The mutillid wasps of the Dasymutilla paradoxa species-group (Hymenoptera, Mutillidae).
Natural history specimen data linked to collectors and determiners held within, "The mutillid wasps of the Dasymutilla paradoxa species-group (Hymenoptera, Mutillidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/c9b07cdc-abd3-44c7-8855-0dbd9bc8ae5f">https://bionomia.net/dataset/c9b07cdc-abd3-44c7-8855-0dbd9bc8ae5f</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/c9b07cdc-abd3-44c7-8855-0dbd9bc8ae5f">https://gbif.org/dataset/c9b07cdc-abd3-44c7-8855-0dbd9bc8ae5f</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: A second species of the family Eutrachytidae (Acari: Uropodina) in Africa: Mahnertellina paradoxa gen. nov., sp. nov. from the Ivory Coast.
Natural history specimen data linked to collectors and determiners held within, "A second species of the family Eutrachytidae (Acari: Uropodina) in Africa: Mahnertellina paradoxa gen. nov., sp. nov. from the Ivory Coast". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/e2cecfdf-c3ab-4588-9216-b014f09da8ef">https://bionomia.net/dataset/e2cecfdf-c3ab-4588-9216-b014f09da8ef</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/e2cecfdf-c3ab-4588-9216-b014f09da8ef">https://gbif.org/dataset/e2cecfdf-c3ab-4588-9216-b014f09da8ef</a>. Formatted as a Frictionless Data package.
Fig. 13. Limnadopsis paradoxa n in A Revision of the Australian Endemic Clam Shrimp Genus Limnadopsis Spencer & Hall (Crustacea: Branchiopoda: Spinicaudata: Limnadiidae)
Fig. 13. Limnadopsis paradoxa n.sp., Sieda Farm, Grass Patch, WA. Male: (A) carapace; (B) head; (C) telson; (D) second clasper. Female: (E) carapace; (F) head; (G) telson. For clarity some growth lines of the carapace are incompletely shown anterior to umbo. Scale bars 1 mm.
Figs 7–9 in Even more paradoxical: Paradoxa paradoxa sp. n. (Diptera: Mycetophilidae) from South Africa, closest relative of the New Zealand Paradoxa fusca Marshall
Figs 7–9. Paradoxa paradoxa sp. n.: (7) male terminalia, ventral view; (8) male terminalia, dorsal view; (9) aedeagal complex and associated structures, lateral view. Abbreviations: A – ejaculatory apodeme; B – aedeagal complex; C – cercus; D – dorsal lobe of gonocoxite; E – gonocoxite; F – gonostylus; G – hypoproct; H – sternite 9; I – tergite 9; J – transverse ridge on gonocoxite; K – ventral lobe of gonocoxite; L – parameral apodeme; M – anterior portion of gonocoxal apodeme; N – posterior portion of gonocoxal apodeme. Scale bar = 0.05 mm (Fig. 9) and 0.1 mm (Figs 7 and 8).
Rosa arvensis Huds. var. paradoxa (BR0000008063762)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Rosa arvensis Huds. var. paradoxa (BR0000008063885)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Rosa arvensis Huds. var. paradoxa (BR0000008063656)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Rosa arvensis Huds. var. paradoxa (BR0000008063946)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Rosa arvensis Huds. var. paradoxa (BR0000008063779)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Iryanthera paradoxa (Schwacke) Warb. from Colombia collected by A. Camargo, E. Álvarez, F. Toro #150
<p><strong>File Name</strong>: <span>TOLI-26246-ZAR-05-138.jpg</span></p> <p><strong>CÓDIGO FOTO</strong>: <span>TOLI-26246-ZAR-05-138-</span></p> <p><strong>Fotografía</strong>: <span>SI</span></p> <p><strong>Nº TOLI</strong>: <span>TOLI-26246</span></p> <p><strong>PARCELA</strong>: <span>ZAR-05</span></p> <p><strong>CÓDIGO</strong>: <span>138</span></p> <p><strong>Nº COLECTA</strong>: <span>150</span></p> <p><strong>NUEVOS COLECTORES</strong>: <span>Alejandro Camargo, Felipe Toro & Esteban Alvarez</span></p> <p><strong>COLECTORES</strong>: <span>A. Camargo, E. Álvarez, F. Toro</span></p> <p><strong>Nº MUESTRAS MONTADAS</strong>: <span>2</span></p> <p><strong>Homologación</strong>: <span>No homologado</span></p> <p><strong>Nueva fecha del evento </strong>: <span>30/11/2018.</span></p> <p><strong>Fecha del evento</strong>: <span>27/04/2019.</span></p> <p><strong>Proyecto </strong>: <span>Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana</span></p> <p><strong>Continente</strong>: <span>SA</span></p> <p><strong>Pais</strong>: <span>Colombia</span></p> <p><strong>Estado/Provincia</strong>: <span>Amazonas</span></p> <p><strong>Municipio</strong>: <span>Leticia</span></p> <p><strong>Localidad</strong>: <span>Resguardo Indígena Ticuna-Huitoto Km 6-11.</span></p> <p><strong>Elevación minima en metros</strong>: <span>200</span></p> <p><strong>Elevación maxima en metros</strong>: <span>300</span></p> <p><strong>Latitud</strong>: <span>-4.004</span></p> <p><strong>Longitud original</strong>: <span>-69.896</span></p> <p><strong>datum geodésico</strong>: <span>WGS 84</span></p> <p><strong>Latitud decimal</strong>: <span>-4.004</span></p> <p><strong>Longitud decimal</strong>: <span>-69.896</span></p> <p><strong>Identificado por</strong>: <span>Diego Suescún </span></p> <p><strong>Fecha de identificación</strong>: <span>25/01/2019.</span></p> <p><strong>Nombre cientifico</strong>: <span>Iryanthera paradoxa (Schwacke) Warb.</span></p> <p><strong>Reino</strong>: <span>Plantae</span></p> <p><strong>Filo</strong>: <span>Magnoliophyta</span></p> <p><strong>Clase</strong>: <span>Equisetopsida</span></p> <p><strong>Orden</strong>: <span>Magnoliales</span></p> <p><strong>Familia nueva</strong>: <span>Myristicaceae</span></p> <p><strong>Género nuevo</strong>: <span>Iryanthera </span></p> <p><strong>especie nueva</strong>: <span>paradoxa </span></p> <p><strong>Autoría del nombre científico</strong>: <span>(Schwacke) Warb.</span></p> <p><strong></strong>: <span>Myristicaceae</span></p> <p><strong>genero herbario</strong>: <span>Iryanthera</span></p> <p><strong>especie herbario</strong>: <span>paradoxa</span></p> <p><strong>Especie de herbario para TNRS</strong>: <span>Iryanthera paradoxa</span></p> <p><strong>Especie corregida herbario y desde TNRS</strong>: <span>Iryanthera paradoxa</span></p> <p><strong>Familia corregida desde TNRS</strong>: <span>Myristicaceae</span></p> <p><strong></strong>: <span>5232</span></p>
Plate 1 in Reproduction Performance, Serum Biochemical and Growth Indices of Grower Rabbits (Oryctolagus cuniculus) fed Sheabutter (Vitellaria paradoxa C.F. Gaertn.) Nut Meal
Plate 1. Uterus of the dead doe showing four embryos
FIGURE 2 in Advertisement call and diel pattern of Pseudis platensis (Anura, Hylidae, Pseudinae) in the Brazilian Pantanal and a bioacoustical comparison with Pseudis paradoxa
FIGURE 2. Diel pattern of calling activity of Pseudis platensis in the Pantanal Matogrossense National Park (Poconé municipality, Mato Grosso, Brazil). Calling activity was measured by acoustic monitoring from 20 January to 2 February 2014 at one site. The diel pattern is expressed as a mean percentage of calls detected at each recording time. Hours are expressed in winter local time (GMT -4). Photo: Mauro Teixeira Jr. © (Cáceres, Mato Grosso, Brazil).
FIGURE 1 in Advertisement call and diel pattern of Pseudis platensis (Anura, Hylidae, Pseudinae) in the Brazilian Pantanal and a bioacoustical comparison with Pseudis paradoxa
FIGURE 1. Oscillogram (Amplitude, ku) and audiospectrogram (Frequency range, kHz) of the advertisement call of Pseudis platensis recorded on 27 January 2013 in the Pantanal Matogrossense National Park, municipality of Poconé, state of Mato Grosso, Brazil. The call was recorded using a Song Meter SM2 recorder at 7:15 p.m., and the mean air temperature was 20ºC. The figure was created using Raven Pro 1.5 with the following configuration: Hamming window function; 64% brightness; 74% contrast; 256 point DFT size; 50% time grid overlap; and Jet Black color scheme.
FIGURE 3. 3-D in Advertisement call and diel pattern of Pseudis platensis (Anura, Hylidae, Pseudinae) in the Brazilian Pantanal and a bioacoustical comparison with Pseudis paradoxa
FIGURE 3. 3-D graph showing the distribution of Pseudis platensis (black circles) and Pseudis paradoxa (empty circles) advertisement calls according to three acoustical parameters. The rectangle highlights the position of the advertisement call described in the present work.
Data from: Morphological and genetic discrepancies in populations of Oreocarya paradoxa and O. revealii: the impact of edaphic selection on recent diversification in the Colorado Plateau
PREMISE OF THE STUDY: Investigations of recently derived and edaphically (soil) defined plant systems have provided insight into important mechanisms of ecological divergence. We investigated the impact of edaphic adaptation on recent divergence between two Colorado Plateau endemics: the gypsum facultative Oreocarya revealii (Boraginaceae) and its more generalist sister species O. paradoxa. We assessed morphological stability, genetic identity, and soil chemistry to determine whether O. revealii is a distinct lineage edaphically adapted from O. paradoxa, as has been described in the literature. METHODS: We genotyped 21 populations throughout the ranges of both species using 11 microsatellite markers and three plastid regions (trnL-F, trnT-L, trnQ-rps16) for haplotype analysis. We compared these data with soil chemistry (Ca and S concentrations, indicating gypsum levels), location, and morphological identity of populations. KEY RESULTS: Soil chemistry failed to explain genetic or morphological identity in either taxon. Haplotype analysis suggests ancestral variation in the more geographically restricted O. revealii, along with regional geographic isolation. A discontinuity was identified between the morphological and genetic identity in several populations, suggesting incomplete lineage sorting and the nonfixation of identifying morphological traits. CONCLUSIONS: Oreocarya revealii is unlikely to have arisen via edaphic selection, because soil chemistry of population sites, morphology of individuals, and genetic identity are not strongly correlated. The nonfixation of identifying traits is likely a result of recent divergence in this system, and the potentiality of such discrepancies should be considered when investigating recently diversified gypsum-associated groups.
FIGURES 21–26 in The mutillid wasps of the Dasymutilla paradoxa species-group (Hymenoptera, Mutillidae)
FIGURES 21–26. Dasymutilla paradoxa species-group, ♂. 21. D. relata, head, anterior view; 22. D. relata, habitus, lateral view; 23. D. sleipniri, head, anterior view; 24. D. sleipniri, habitus, lateral view; 25. D. naranjo, axillae, dorsal view; 26. D. sleipniri, axillae, dorsal view.
FIGURES 15–20 in The mutillid wasps of the Dasymutilla paradoxa species-group (Hymenoptera, Mutillidae)
FIGURES 15–20. Dasymutilla paradoxa species-group, ♂. 15. D. fasciventris, head, anterior view; 16. D. fasciventris, habitus, lateral view; 17. D. guanacaste, head, anterior view; 18. D. guanacaste, habitus, lateral view; 19. D. naranjo, head, anterior view; 20. D. naranjo, habitus, lateral view.
FIGURES 9–14 in The mutillid wasps of the Dasymutilla paradoxa species-group (Hymenoptera, Mutillidae)
FIGURES 9–14. Dasymutilla paradoxa species-group, ♀. 9. D. paradoxa, head, anterior view; 10. D. paradoxa, pygidium, dorsal view; 11. D. paraparadoxa sp. nov., head, anterior view; 12. D. paraparadoxa sp. nov., pygidium, dorsal view; 13. D. phya, head, anterior view; 14. D. phya, pygidium, dorsal view.
FIGURES 1–8 in The mutillid wasps of the Dasymutilla paradoxa species-group (Hymenoptera, Mutillidae)
FIGURES 1–8. Dasymutilla paradoxa species-group, ♀. 1. D. fasciventris, habitus, dorsal view; 2. D. fasciventris, habitus, lateral view; 3. D. paradoxa, habitus, dorsal view; 4. D. paradoxa, habitus, lateral view; 5. D. paraparadoxa sp. nov., habitus, dorsal view; 6. D. paraparadoxa sp. nov., habitus, lateral view; 7. D. phya, habitus, dorsal view; 8. D. phya, habitus, dorsal view. Scale bars: 1 mm.
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