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1.
Ying Yong Sheng Tai Xue Bao ; 29(11): 3705-3711, 2018 Nov.
Artigo em Chinês | MEDLINE | ID: mdl-30460818

RESUMO

To examine the change of runoff and its reason is an important scientific issue in forest hydrology. In this study, we performed the trend and inflection analysis on the time series of daily precipitation and runoff in the Pengchongjian small watershed from 1983 to 2014 by Mann-Kendall test method, a site with abundant precipitation . Using the empirical statistics method, we analyzed the effects of precipitation variation and vegetation restoration on the runoff and its contribution rates. Furthermore, we calculated the critical value of the hydrological effect of vegetation restoration on the annual precipitation. The results showed that the year 2003 was a consistent abrupt point for annual precipitation and runoff. Compared to the baseline period (1983-2003), annual precipitation and the depth of runoff in the changing period (2004-2014) decreased by 8.7% and 29.2%, with the averaged annual decrease of 12.7 and 22.1 mm, respectively. The averaged depth of runoff in spring, summer, autumn, winter, and in the whole year decreased by 100.2, 105.8, 25.2, 23.4, and 243.0 mm, respectively. The contribution rates of the depth of runoff to precipitation varia-tion were 58.9%, 71.6%, 65.5%, 35.0%, and 57.1%, respectively, while the contribution rates of vegetation restoration were 41.1%, 28.4%, 34.5%, 65.0%, and 42.9%, respectively. The hydrological effect of vegetation restoration was attributed to the annual precipitation, with a critical value of 1181 mm. Vegetation restoration increased annual depth of runoff when annual precipitation was less than the critical value, and increased that when annual precipitation was higher than the critical value. Therefore, the critical value might help to explain the difference in contribution rates of vegetation restoration to runoff in different watersheds and serve as one of the important reasons for the debate and divergence of forest restoration impacts on runoff.


Assuntos
Recuperação e Remediação Ambiental , Florestas , China , Hidrologia , Movimentos da Água
2.
Med Sci Monit Basic Res ; 21: 241-6, 2015 Nov 26.
Artigo em Inglês | MEDLINE | ID: mdl-26609771

RESUMO

BACKGROUND The endogenous protein annexin A1 (ANXA1) is an anti-inflammatory mediator in the brain that is thought to contribute to the progression of many neurological conditions. However, its exact role in temporal lobe epilepsy (TLE) remains unclear. We hypothesized that ANXA1 exerts negative actions on TLE by alleviating inflammatory damage in neurons. To identify the potential mechanism of TLE by assessing ANXA1 expression in TLE rats. MATERIAL AND METHODS TLE was induced in rats (n=70) via an intraperitoneal injection of lithium chloride (LiCl) and pilocarpine (PILO). The control group (n=10) received an injection of the equivalent amount of saline. ANXA1 expression was detected via immunohistochemistry and Western blotting. RESULTS Successful establishment of the TLE model in rats resulted in epileptic seizures. ANXA1 was immunohistochemically detected as brownish yellow particles in the dentate gyrus and the CA1 region of the door zone; this expression was predominantly localized to the cytoplasm of glia rather than neurons. ANXA1 expression was stronger in TLE rats compared with the control group. ANXA1 expression in TLE was also assessed via Western blotting, and compared between groups at various time points. ANXA1 expression was significantly increased in the acute (the first 24 h) and chronic (after 1 month) phases (P<0.001) but significantly decreased during the recovery phase (72 h, 1 week, and 2 weeks) (P<0.001). These findings suggest that ANXA1 expression is correlated with TLE activity. CONCLUSIONS Our data suggest that ANXA1 plays an important role in TLE by alleviating inflammatory damage and protecting neurons.


Assuntos
Anexina A1/biossíntese , Epilepsia do Lobo Temporal/metabolismo , Animais , Encéfalo/metabolismo , Encéfalo/patologia , Modelos Animais de Doenças , Epilepsia do Lobo Temporal/induzido quimicamente , Epilepsia do Lobo Temporal/patologia , Epilepsia do Lobo Temporal/fisiopatologia , Hipocampo/metabolismo , Hipocampo/patologia , Masculino , Distribuição Aleatória , Ratos , Ratos Sprague-Dawley
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