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1.
J Biogeogr ; 49(5): 979-992, 2022 May.
Artículo en Inglés | MEDLINE | ID: mdl-35506011

RESUMEN

Aim: Comprehensive, global information on species' occurrences is an essential biodiversity variable and central to a range of applications in ecology, evolution, biogeography and conservation. Expert range maps often represent a species' only available distributional information and play an increasing role in conservation assessments and macroecology. We provide global range maps for the native ranges of all extant mammal species harmonised to the taxonomy of the Mammal Diversity Database (MDD) mobilised from two sources, the Handbook of the Mammals of the World (HMW) and the Illustrated Checklist of the Mammals of the World (CMW). Location: Global. Taxon: All extant mammal species. Methods: Range maps were digitally interpreted, georeferenced, error-checked and subsequently taxonomically aligned between the HMW (6253 species), the CMW (6431 species) and the MDD taxonomies (6362 species). Results: Range maps can be evaluated and visualised in an online map browser at Map of Life (mol.org) and accessed for individual or batch download for non-commercial use. Main conclusion: Expert maps of species' global distributions are limited in their spatial detail and temporal specificity, but form a useful basis for broad-scale characterizations and model-based integration with other data. We provide georeferenced range maps for the native ranges of all extant mammal species as shapefiles, with species-level metadata and source information packaged together in geodatabase format. Across the three taxonomic sources our maps entail, there are 1784 taxonomic name differences compared to the maps currently available on the IUCN Red List website. The expert maps provided here are harmonised to the MDD taxonomic authority and linked to a community of online tools that will enable transparent future updates and version control.

2.
Sci Robot ; 2(7)2017 06 21.
Artículo en Inglés | MEDLINE | ID: mdl-33157896

RESUMEN

Modern telerobotic technologies offer astronaut scientists real-time presence on planetary surfaces without the risk and cost of putting them all the way there.

4.
PLoS One ; 8(5): e64479, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23704988

RESUMEN

Puccinia psidii sensu lato (s.l.) is an invasive rust fungus threatening a wide range of plant species in the family Myrtaceae. Originating from Central and South America, it has invaded mainland USA and Hawai'i, parts of Asia and Australia. We used CLIMEX to develop a semi-mechanistic global climatic niche model based on new data on the distribution and biology of P. psidii s.l. The model was validated using independent distribution data from recently invaded areas in Australia, China and Japan. We combined this model with distribution data of its potential Myrtaceae host plant species present in Australia to identify areas and ecosystems most at risk. Myrtaceaeous species richness, threatened Myrtaceae and eucalypt plantations within the climatically suitable envelope for P. psidii s.l in Australia were mapped. Globally the model identifies climatically suitable areas for P. psidii s.l. throughout the wet tropics and sub-tropics where moist conditions with moderate temperatures prevail, and also into some cool regions with a mild Mediterranean climate. In Australia, the map of species richness of Myrtaceae within the P. psidii s.l. climatic envelope shows areas where epidemics are hypothetically more likely to be frequent and severe. These hotspots for epidemics are along the eastern coast of New South Wales, including the Sydney Basin, in the Brisbane and Cairns areas in Queensland, and in the coastal region from the south of Bunbury to Esperance in Western Australia. This new climatic niche model for P. psidii s.l. indicates a higher degree of cold tolerance; and hence a potential range that extends into higher altitudes and latitudes than has been indicated previously. The methods demonstrated here provide some insight into the impacts an invasive species might have within its climatically suited range, and can help inform biosecurity policies regarding the management of its spread and protection of valued threatened assets.


Asunto(s)
Basidiomycota/crecimiento & desarrollo , Clima , Ecosistema , Especificidad del Huésped , Especies Introducidas , Modelos Biológicos , Myrtaceae/microbiología , Agar/farmacología , Australia , Basidiomycota/efectos de los fármacos , Geografía , Reproducibilidad de los Resultados , Temperatura , Madera/microbiología
5.
Astrobiology ; 8(4): 781-92, 2008 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-18752458

RESUMEN

We present data in examination of the utility of electrical impedance spectroscopy measurements for in situ surveys to determine the water content, distribution, and phase in unconsolidated planetary regolith. We conducted calibration experiments under conditions relevant to Mars: the concentration of electrolytes in solution was varied up to 1 M to simulate the effects of unsaturated dissolved minerals and brines. We also varied the water content of heterogeneous water/sand mixtures, made with these electrolytic solutions from 0.01 wt% to 10 wt%. Tests were performed at temperatures from +25 degrees C to -65 degrees C. Conductivity and dielectric permittivity calculated from the impedance measurements indicate an expected dependence on electrolyte concentration and relative independence from electrolyte type for both liquid water and water ice. Conductivity and calculated dielectric relaxation times for these aqueous solutions agree with existing data in the literature. The relative permittivity for heterogeneous water/sand mixtures is dominated by polarization effects for the electrode configuration used. However, the characteristic orientational relaxation of ice is still visible. The conductivity retains the strong dependence on electrolyte concentration, and the permittivity is still not affected by electrolyte type. A "universal" curve between conductivity and water content establishes detectability limits of <0.01 wt% and approximately 0.3 wt% for water/sand mixtures containing liquid water and ice, respectively.


Asunto(s)
Impedancia Eléctrica , Calibración , Conductividad Eléctrica , Electroquímica/métodos , Electrodos , Electrólitos , Diseño de Equipo , Exobiología/métodos , Enlace de Hidrógeno , Hielo , Planetas , Análisis Espectral/métodos , Temperatura , Termodinámica , Agua/química , Agua/metabolismo
6.
Dermatitis ; 17(1): 36-8, 2006 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-16800277

RESUMEN

We describe a patient with Stevens-Johnson syndrome (erythema multiforme major) associated with an increase in glipizide dosage administration. Glipizide is a second-generation sulfonylurea commonly used to treat patients with noninsulin-dependent diabetes mellitus. Although several reports have documented Stevens-Johnson syndrome caused by first-generation sulfonylureas, our case appears to be the first report of a second-generation sulfonylurea associated with Stevens-Johnson syndrome.


Asunto(s)
Diabetes Mellitus Tipo 2/tratamiento farmacológico , Glipizida/efectos adversos , Síndrome de Stevens-Johnson/inducido químicamente , Síndrome de Stevens-Johnson/patología , Adulto , Biopsia con Aguja , Diabetes Mellitus Tipo 2/diagnóstico , Estudios de Seguimiento , Glipizida/uso terapéutico , Humanos , Inmunohistoquímica , Masculino , Enfermedades Raras , Índice de Severidad de la Enfermedad
7.
Pediatr Dermatol ; 22(2): 122-6, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15804299

RESUMEN

Three siblings, two boys and one girl, presented with pigmentary abnormalities. The brothers, ages 11 and 6 years, had diffuse reticulate macular hyperpigmentation with onset in early childhood. In addition, these boys had hypohydrosis, coarse hair with an upswept frontal hairline, failure to thrive, and chronic pulmonary disease. The older boy also had corneal dystrophy and marked photophobia. A punch biopsy specimen from the 11-year-old showed melanophages and necrotic keratinocytes. Stains for amyloid were negative. The sister, age 2 years, had congenital linear hyperpigmented patches involving the intertrigenous areas, but was otherwise normal. The clinical findings of these children were consistent with X-linked reticulate pigmentary disorder with systemic manifestations. We present a summary of the clinical manifestations of this rare disorder and discuss efforts to identify the causative gene.


Asunto(s)
Enfermedades Genéticas Ligadas al Cromosoma X/diagnóstico , Trastornos de la Pigmentación/diagnóstico , Piel/patología , Niño , Preescolar , Distrofias Hereditarias de la Córnea/complicaciones , Insuficiencia de Crecimiento/complicaciones , Femenino , Enfermedades Genéticas Ligadas al Cromosoma X/complicaciones , Humanos , Masculino , Fotofobia/complicaciones , Trastornos de la Pigmentación/complicaciones
8.
J Am Acad Dermatol ; 51(5): 820-3, 2004 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-15523368

RESUMEN

The West Nile Virus (WNV) has rapidly emerged as an important etiology of meningoencephalitis in North America since 1999. Diagnosis of this infection on clinical grounds is difficult, as many signs and symptoms of infection are nonspecific. Although cutaneous manifestations are common in WNV-infected patients, these have not been described in detail nor are clinical images widely available. We describe 3 patients with WNV infections, two ambulatory, one hospitalized, who developed punctate erythematous, macular, and papular eruptions, most pronounced on the extremities. Histopathologic findings in one case showed a sparse superficial perivascular lymphocytic infiltrate, a feature commonly seen in viral exanthems but not previously reported with WNV infection. A literature review provides support that this punctate exanthem is a common cutaneous presentation of WNV infection.


Asunto(s)
Exantema/patología , Extremidades/patología , Fiebre del Nilo Occidental/patología , Adulto , Anciano , Diagnóstico Diferencial , Exantema/virología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Virus del Nilo Occidental
9.
Gene Expr Patterns ; 3(1): 77-82, 2003 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-12609607

RESUMEN

The only molecular similarity shown so far for sexual regulatory genes among different phyla involves doublesex (dsx) of Drosophila, mab-3 and mab-23 of Caenorhabditis elegans, and Dmrt1 of vertebrates. These genes encode DM domain transcription factors (DM = dsx and mab-3) and are required for sexual differentiation. In the case of dsx and mab-3, the two genes control analogous aspects of sexual development, bind similar DNA sequences, and are capable of functional substitution in vivo. All three phyla have multiple DM domain genes, but it is unknown how many of these are involved in sexual development. Mammals, for example, have at least seven DM domain genes, but embryonic expression has only been examined in detail for Dmrt1(dsx- and mab-3 related transcription factor 1). We have identified additional murine DM domain genes and have examined their expression in the mouse embryo, with emphasis on the developing gonad. At least three murine DM domain genes in addition to Dmrt1 are expressed in the embryonic gonad: Dmrt4 is expressed at similar levels in gonads of both sexes; Dmrt3 is more highly expressed in males; and Dmrt7 is more highly expressed in females. Expression of three other genes is low or absent in the embryonic gonad. Two of these, Dmrt5 and Dmrt6, are expressed primarily in the brain, and the third, Dmrt2, is expressed in presomitic mesoderm and developing somites. Our data suggest that multiple DM domain genes may be involved in mammalian sexual development, and that they may function in both testis and ovary development.


Asunto(s)
Proteínas de Unión al ADN/genética , Proteínas de Drosophila/genética , Perfilación de la Expresión Génica , Ovario/embriología , Testículo/embriología , Animales , Proteínas de Caenorhabditis elegans/genética , Mapeo Cromosómico , Proteínas de Unión al ADN/metabolismo , Femenino , Masculino , Ratones , Datos de Secuencia Molecular , Especificidad de Órganos , Ovario/metabolismo , Testículo/metabolismo , Factores de Transcripción/genética , Factores de Transcripción/metabolismo
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