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1.
Water Environ Res ; 92(12): 2178-2192, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-31995847

RESUMO

Stormwater best management practices (BMPs) help mitigate the adverse effects of urban development on stream hydrology and water quality, and are widely specified in development requirements and watershed management plans. However, design of stormwater BMPs largely relies on experience with historic climate, which may not be a reliable guide to the future. To inform BMP design that is robust to future conditions, it is important to examine how potential changes in precipitation, temperature, and potential evapotranspiration will affect the performance of BMPs. We use continuous simulation modeling to examine BMP performance under current and potential future climatic conditions and determine the changes needed in site configuration to address future impacts. We perform modeling for five development types in five different regions of the United States and explore both conventional ("gray") and green infrastructure (GI) stormwater management approaches. If stormwater designs are adapted to address potential future climate conditions, this study suggests that the most cost-effective approaches may use both gray and green BMPs. If the magnitude of extreme weather events increases dramatically, then gray practices that provide detention storage may have better cost-effectiveness. Incorporating risk of future climate impacts into stormwater design may help communities become more resilient. PRACTITIONER POINTS: There is a risk that projected changes in meteorological forcing will negatively affect stormwater BMP performance. Under projected future climate conditions, this study suggests the most cost-effective approaches may use both gray and green BMPs. If the magnitude of extreme weather events increases dramatically, gray practices that provide detention storage may have better cost-effectiveness. Flexibility is beneficial in adaptation and resilience planning due to uncertainty in projected precipitation volume and intensity changes.


Assuntos
Hidrologia , Chuva , Simulação por Computador , Rios , Qualidade da Água
2.
J Neurosci Res ; 86(12): 2602-14, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18478542

RESUMO

An Ig superfamily cell-adhesion molecule, L1, forms an adhesion complex at the cell membrane containing both signaling molecules and cytoskeletal proteins. This complex mediates the transduction of extracellular signals and generates actin-mediated traction forces, both of which support axon outgrowth. The L1 cytoplasmic region binds ezrin, an adapter protein that interacts with the actin cytoskeleton. In this study, we analyzed L1-ezrin interactions in detail, assessed their role in generating traction forces by L1, and identified potential regulatory mechanisms controlling ezrin-L1 interactions. The FERM domain of ezrin binds to the juxtamembrane region of L1, demonstrated by yeast two-hybrid interaction traps and protein binding analyses in vitro. A lysine-to-leucine substitution in this domain of L1 (K1147L) shows reduced binding to the ezrin FERM domain. Additionally, in ND7 cells, the K1147L mutation inhibits retrograde movement of L1 on the cell surface that has been linked to the generation of the traction forces necessary for axon growth. A membrane-permeable peptide consisting of the juxtamembrane region of L1 that can disrupt endogenous L1-ezrin interactions inhibits neurite extension of cerebellar cells on L1 substrates. Moreover, the L1-ezrin interactions can be modulated by tyrosine phosphorylation of the L1 cytoplasmic region, namely, Y1151, possibly through Src-family kinases. Replacement of this tyrosine together with Y1176 with either aspartate or phenylalanine changes ezrin binding and alters colocalization with ezrin in ND7 cells. Collectively, these data suggest that L1-ezrin interactions mediated by the L1 juxtamembrane region are involved in traction-force generation and can be regulated by the phosphorylation of L1.


Assuntos
Proteínas do Citoesqueleto/metabolismo , Molécula L1 de Adesão de Célula Nervosa/metabolismo , Tirosina/metabolismo , Células 3T3 , Animais , Sítios de Ligação/fisiologia , Membrana Celular/metabolismo , Proteínas do Citoesqueleto/fisiologia , Citoesqueleto/fisiologia , Espaço Extracelular/fisiologia , Humanos , Camundongos , Molécula L1 de Adesão de Célula Nervosa/fisiologia , Neuritos/fisiologia , Fosforilação/fisiologia , Ratos , Transdução de Sinais/fisiologia
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