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1.
Zootaxa ; 4951(2): zootaxa.4951.2.5, 2021 Apr 06.
Artículo en Inglés | MEDLINE | ID: mdl-33903404

RESUMEN

We review Irestedt et al.'s (2017) neotypification of the senior species name superba Pennant, 1781 in the bird-of-paradise genus Lophorina in response to Elliott et al. (2020) who challenged the resultant shift in name from the small isolate in New Guinea's Vogelkop to the widespread species in the island's central cordillera. In nine male plumage traits which differentiate the two species, six of which had been identified as novel by Irestedt et al., we show that the only two figures of the perished male holotype of superba match the central cordillera species more closely than the Vogelkop. We find as well that not only was the trading of bird-of-paradise skins from the central cordillera to coastal ports in the Vogelkop feasible before European contact, but application of superba to the central cordillera species also promotes nomenclatural stability: the name has been used overwhelmingly at species rank for that widespread form throughout post-19th century media. Re-assessment of Irestedt et al.'s point-by-point justification of neotypification under Article 75.3 of the ICZN (1999) Code establishes, furthermore, that their case meets the requirements of every condition specified in the article; the neotypification is thus valid. Elliott et al.'s alternative to fix superba to the Vogelkop isolate by type locality restriction is not Code-compliant, nor is their evidence for interpreting J.R. Forster as the author of the name. In conclusion, we lay out the correct nomenclature for the taxa of Lophorina under the Code.


Asunto(s)
Passeriformes , Animales , Masculino , Passeriformes/clasificación
2.
Heredity (Edinb) ; 120(2): 138-153, 2018 01.
Artículo en Inglés | MEDLINE | ID: mdl-29225353

RESUMEN

Invasive species exert a serious impact on native fauna and flora and have been the target of many eradication and management efforts worldwide. However, a lack of data on population structure and history, exacerbated by the recency of many species introductions, limits the efficiency with which such species can be kept at bay. In this study we generated a novel genome of high assembly quality and genotyped 4735 genome-wide single nucleotide polymorphic (SNP) markers from 78 individuals of an invasive population of the Javan Myna Acridotheres javanicus across the island of Singapore. We inferred limited population subdivision at a micro-geographic level, a genetic patch size (~13-14 km) indicative of a pronounced dispersal ability, and barely an increase in effective population size since introduction despite an increase of four to five orders of magnitude in actual population size, suggesting that low population-genetic diversity following a bottleneck has not impeded establishment success. Landscape genomic analyses identified urban features, such as low-rise neighborhoods, that constitute pronounced barriers to gene flow. Based on our data, we consider an approach targeting the complete eradication of Javan Mynas across Singapore to be unfeasible. Instead, a mixed approach of localized mitigation measures taking into account urban geographic features and planning policy may be the most promising avenue to reducing the adverse impacts of this urban pest. Our study demonstrates how genomic methods can directly inform the management and control of invasive species, even in geographically limited datasets with high gene flow rates.


Asunto(s)
Flujo Génico , Genética de Población , Especies Introducidas , Passeriformes/genética , Animales , Ciudades , Genómica , Polimorfismo de Nucleótido Simple , Densidad de Población , Singapur , Análisis Espacial
5.
Acta Derm Venereol ; 67(3): 265-7, 1987.
Artículo en Inglés | MEDLINE | ID: mdl-2442945

RESUMEN

In a patient with total C2 deficiency and repeated respiratory infections a papulovesicular rash showed to be due to leukocytoclastic vasculitis. The patient's brother also had a total deficiency of C2 but no clinical symptoms. HLA-investigation in both him and the proband showed the genotype commonly reported in cases with homozygous C2 deficiency. Their heterozygous mother and sister had slightly decreased C2 levels.


Asunto(s)
Complemento C2/deficiencia , Vasculitis/inmunología , Adulto , Dermatitis Atópica/diagnóstico , Diagnóstico Diferencial , Femenino , Antígenos HLA/análisis , Heterocigoto , Homocigoto , Humanos , Masculino , Vasculitis/diagnóstico
6.
Acta Derm Venereol ; 66(1): 67-70, 1986.
Artículo en Inglés | MEDLINE | ID: mdl-2424221

RESUMEN

Extremely low C4 values were found in a 65-year-old man with relapsing arthritis and skin lesions of many years duration of the scalp, face, hands and feet together with painful ulcerations of the toes and fingers. The discovery was made during an exacerbation, but the deficiency of C4 persisted in repeated controls after remission. The clinical findings in connection with these low C4 values are in congruence with the diagnosis of inherited deficiency of C4.


Asunto(s)
Complemento C4/deficiencia , Lupus Eritematoso Sistémico/genética , Anciano , Artritis/genética , Complemento C1/análisis , Proteínas Inactivadoras del Complemento 1/análisis , Complemento C2/análisis , Complemento C3/análisis , Humanos , Inmunoglobulina M/análisis , Lupus Eritematoso Sistémico/inmunología , Masculino , Enfermedades de la Piel/genética
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