RESUMEN
Since the establishment of the world-class Three Gorges Dam (TGD) across the Yangtze River, China, the downstream reach has experienced a long-term adjustment with regard to the river morphology and hydrodynamics, imposing a profound impact on the environmental conditions of human living and aquatic ecosystem. This study presents an investigation on the river channel morphological characteristics and hydrodynamic environment of a large bifurcation-confluence complex downstream of the TGD through detailed field survey and numerical modeling. Results show that the main stem, before being bifurcated into two sub-channels (the North Channel and the South Channel), experiences a meander, leading to the severe bed scouring near the outer bank (pools) resulted from a high flow mass flux and bed shear stress. Because of being bifurcated, the river width with largely growing may result in the reduction of flow velocity and sediment deposition (riffles), and thereby two plugbars are formed near the entrance of two sub-channels. In the meantime, the velocity-reversal phenomenon (flow velocity and friction velocity) is identified when low flows are transited into high flows. The flow mass flux, however, is always larger in pool regions, which is highly related to water depth. As a result, the topographic steering of flows by riffles, bars and floodplains may have more impact on flow path under low flow conditions, while the bankline shape would become more important under high flows. Furthermore, the topographic steering could play a key role in the pattern of flow separations near the confluence. More interestingly, the confluence flow separation only occurs under low flow conditions and its occurring location shifts upwards the tributary (the North Channel), which differs from observations in previous studies. The visualized numerical results of friction velocity distribution indicate that sediment is more likely to deposit in the North Channel (entrance) with lower friction velocity, implying the potential closure of the sub-channel.
RESUMEN
(Z)-4-(4-Methoxyphenoxy)-4-oxobut-2-enoic acid and its solid rare earth complexes LnL3.2H2O (Ln=La, Eu, Tb) were synthesized and characterized by means of MS, elemental analysis, FTIR, 13C NMR and TG-DTA. The IR and 13C NMR results show that the carboxylic groups in the complexes coordinated to the rare earth ions in the form of a bidentate ligand, but the ester carboxylic groups have not taken part in the coordination. The luminescence spectra of Eu(III) and Tb(III) complexes in solid state were also studied. The strong luminescence emitting peaks at 616nm for Eu(III) and 547nm for Tb(III) can be observed, which could be attributed to the ligand has an enhanced effect to the luminescence intensity of the Eu and Tb.
