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1.
Tree Physiol ; 26(1): 87-92, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16203718

RESUMO

Recovery of water status in water-stressed pistachio trees (Pistacia vera L. cv. Kerman) was investigated by subjecting trees to regulated deficit irrigation (RDI) (60% of crop evapotranspiration rate, ET(c)) during stages I and II of fruit development (FD) followed by full irrigation during FD stage III (kernel-filling). Trees irrigated at 100% ET(c) throughout FD stages I, II and III served as controls. Water-stress severity was characterized by changes in soil water content and midday stem water potential (Psi(md)). Midday leaf conductance (g(1)) and trunk diameter variation (TDV) were also measured. In RDI trees, the lowest Psi(md) value, -1.8 MPa, occurred at the end of the RDI period. The corresponding value for the control trees was around -1.1 MPa. Although the RDI treatment affected gas exchange later than Psi(md), the greatest reductions in gas exchange (60% of control values) also appeared at the end of the RDI period. There were significant differences in TDV between control and RDI trees at the end of the RDI period. Although plant water status recovered within 20 days of resuming irrigation, the TDV values indicated a longer period might be necessary for complete recovery. Recovery of g(1) was faster than that of Psi(md), although differences in TDV between control and RDI trees indicated that gas exchange recovered later than Psi(md). The slow recovery of pistachio trees during FD stage III from water stress imposed during FD stages I and II suggests that irrigation should exceed 100% ET(c) during FD stage III or that more extensive irrigation should commence before the end of FD stage II.


Assuntos
Pistacia/metabolismo , Água/metabolismo , Pistacia/crescimento & desenvolvimento , Pistacia/fisiologia , Transpiração Vegetal , Solo/análise , Fatores de Tempo , Água/análise
2.
Rev Neurol ; 23(119): 145-7, 1995.
Artigo em Espanhol | MEDLINE | ID: mdl-8548611

RESUMO

Hepatolenticular degeneration, also known as Wilson's disease (WD), is an infrequent hereditary disorder which is transmitted in recessive autosomic fashion: its genetic defect is to be found in the long branch of chromosome 13 (13q14.3) and allows disorder to take place which has not been sufficiently clarified, in the bilious excretion of the copper (Cu) which is deposited in an anomalous manner on a level with different organic tissues, giving rise to characteristic clinical manifestations which are, basically, of a neurological, hepatic, psychiatric and ocular nature. We present the case of a young patient whose case began, four years ago, with depressive-type manifestations, with diagnosis only being made now. Our opinion on the early detection of asymptomatic patients is commented on, along with that concerning the effectiveness and safety of therapeutic alternatives to D-penicilamine.


Assuntos
Córtex Cerebral/fisiopatologia , Degeneração Hepatolenticular/tratamento farmacológico , Degeneração Hepatolenticular/fisiopatologia , Trientina/uso terapêutico , Adulto , Ventrículos Cerebrais/anormalidades , Cromossomos Humanos Par 13 , Cobre/sangue , Feminino , Degeneração Hepatolenticular/diagnóstico , Humanos , Imageamento por Ressonância Magnética , Tomografia Computadorizada por Raios X , Trientina/administração & dosagem
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