三峡库区岸边植物水分利用研究

随着三峡大坝建设，在2003年6月三峡库区蓄水到135 m水位，之后人为调节使其在137-139 m范围内波动变化。从2003年7月开始，我们对库区植物的水分关系及其对三峡水位上升的可能反应进行了系统研究。 在库区中残存的次生松栎混交林，我们从江边沿海拔梯度设置了3块样地：Riparian，Mid-hill和Top-hill样地，垂直高度相差约20 m。从2003年7月到2004年7月，我们比较了岸边样地内与高处两样地内植物的木质部水分稳定同位素D和18O值，植物清晨和中午水势，叶片碳稳定同位素值13C，以及2004年7月测定的气体交换。岸边 植物木质部水分同位素值显著高于江水的同位素值，而与高处两样地内植物木质部水分同位素相近。岸边植物与高 处植物具有相近的清晨水势和中午水势，也表明对岸边植物来说，江水并不是它们重要的水分来源。同样，岸边植 物叶片 13C值与高处同种植物的值也不存在显著差异。我们研究的3种植物清晨水势都与土壤含水量正相关，尤 其浅层土壤更为显著。研究结果表明岸边植物几乎没有利用江水，而同高处两样地内植物一样，都是以利用渗入到土壤中的降雨为主。 松栎混交林中，马尾松与槲栎相比，净光合速率和气孔导度，叶片含N量，以及清晨水势低于槲栎，而中午水势，叶片13C值高于槲栎。两种树木叶片13C值与含N量都成正相关关系。槲栎叶片13C值与清晨水势成负相关，而马尾松针叶13C值与清晨水势相关性并不显著。 在岸边的松栎混交幼林与成年林相比，幼树的清晨水势略高于对应的成年树，叶片13C值低于成年树;幼树的光合速率和气孔导度略高于成年树，而瞬时水分利用效率低于成年树，但差异均不显著。马尾松幼苗为实生苗，与成年树相比，更偏向于利用浅层土壤水;而槲栎幼树多为从原来被砍伐的树上萌生的，木质部水分同位素与成年树相近。 从2004年5月到10月，我们又对大坝下游江段岸边植物（马尾松，枫杨和柑桔）的水分关系进行了研究。木质部水分同位素比率表明，岸边植物木质部水分同位素比率与高处植物具相近的值，且显著高于江水同位素值。研究表明岸岸边和高处植物以降雨或靠降雨补充的浅层地下水为主要水分来源，即便岸边植物也几乎不利用江水。岸边植物与高处植物具有相近的清晨水势和中午水势，光合速率和气孔导度，以及叶片C值等，也进一步说明岸边植物与高处植物具有相近的水分生理特征。 叶片13C可以指示植物的一些生理过程，我们对松栎混交林中不同生活型植物的13C值进行了分析，乔木层叶片 13C值比较高，其中常绿针叶的值又高于落叶阔叶树木的值;林下灌木，非禾本科草本，及藤本植物的13C值都明显低于乔木层。 三峡大坝改变河水对植物生理生态过程的影响是一个长期的过程，库区水位上涨是否影响到岸边植物的生理过程及生长等，需要进一步作长期、定位和连续的观测研究。

Seasonal Variations in Chlorophyll a Concentrations in Relation to Potentials of Sediment Phosphate Release by Different Mechanisms in a Large Chinese Shallow Eutrophic Lake (Lake Taihu)

The relationship between chlorophyll a and fractionation of sediment phosphorus, inorganic phosphate-solubilizing bacteria (IPB), and organic phosphate-mineralizing bacteria (OPB) was evaluated in a large Chinese shallow eutrophic lake (Lake Taihu) and its embayment (Wuli Bay). At the three study sites, the increase of chlorophyll a concentrations in April paralleled those of the iron bound phosphate accounting for major portion of sediment inorganic phosphate, and in June significantly higher OPB and IPB numbers (especially OPB) in sediment were main contributors to the peaks of chlorophyll a concentration. Even though IPB peaked from February to June, it should serve as an unimportant P source due to the irrelevancy with chlorophyll a and soluble reactive phosphorus (SRP). By contrast, at the other site in the embayment, the calcium-bound phosphate was predominant and solid, which was difficult to be released, and neither IPB nor OPB were detectable in the sediment, indicating weak potential for phosphorus release from the sediment, which was reflected in the small seasonal variation in SRP concentration in water column. Hence, the extents to which the three general mechanisms behind phosphate release from sediment (desorption of iron bound phosphate, solubilization by IPB and enzymatic hydrolysis by OPB) operated were different depending on seasons and sites in Lake Taihu, they may jointly drive phosphate release and accelerate the eutrophication processes.

Phosphorus in interstitial water induced by redox potential in sediment of Dianchi Lake, China

The sediment redox potential was raised in the laboratory to estimate reduction of internal available phosphorus loads, such as soluble reactive phosphorus (SRP) and total phosphorus (TP), as well as the main elements of sediment extracts in Dianchi Lake. Several strongly reducing substances in sediments, which mainly originated from anaerobic decomposition of primary producer residues, were responsible for the lower redox potential. In a range of -400 to 200 mV raising the redox potential of sediments decreased TP and SRP in interstitial water. Redox potentials exceeding 320 mV caused increases in TP, whereas SRP maintained a relatively constant minimum level. The concentrations of Al, Fe, Ca2+, Mg2+, K+, Na+ and S in interstitial water were also related to the redox potential of sediments, suggesting that the mechanism for redox potential to regulate the concentration of phosphorus in interstitial water was complex.

On the radiation and diffraction of linear water waves by an infinitely long rectangular structure submerged in oblique seas

The radiation and diffraction of linear water waves by an infinitely long rectangular structure submerged in oblique seas of finite depth is investigated. The analytical expressions for the radiated and diffracted potentials are derived as infinite series by use of the method of separation of variables. The unknown coefficients in the series are determined by the eigenfunction expansion matching method. The expressions for wave forces, hydrodynamic coefficients and reflection and transmission coefficients are given and verified by the boundary element method. Using the present analytical solution, the hydrodynamic influences of the angle of incidence, the submergence, the width and the thickness of the structure on the wave forces, hydrodynamic coefficients, and reflection and transmission coefficients are discussed in detail.

Scattering of linear water waves by a fixed and infinitely long rectangular structure parallel to a vertical wall in oblique seas

The scattering of linear water waves by an infinitely long rectangular structure parallel to a vertical wall in oblique seas is investigated. Analytical expressions for the diffracted potentials are derived using the method of separation of variables. The unknown coefficients in the expressions are determined through the application of the eigenfunction expansion matching method. The expressions for wave forces on the structure are given. The calculated results are compared with those obtained by the boundary element method. In addition, the influences of the wall, the angle of wave incidence, the width of the structure, and the distance between the structure and the wall on wave forces are discussed. The method presented here can be easily extended to the study of the diffraction of obliquely incident waves by multiple rectangular structures.

Charge transfer across the water/nitrobenzene interface by three-electrode system

A droplet of aqueous solution containing a certain molar ratio of redox couple is first attached onto a platinum electrode surface, then the resulting drop electrode is immersed into the organic solution containing very hydrophobic electrolyte. Combined with reference and counter electrodes, a classical three-electrode system has been constructed, Ion transfer (IT) and electron transfer (ET) are investigated systematically using three-electrode voltammetry. Potassium ion transfer and electron transfer between potassium ferricyanide in the aqueous phase and ferrocene in nitrobenzene are observed with potassium ferricyanide/potassium ferrocyanide as the redox couple. Meanwhile, the transfer reactions of lithium, sodium, potassium, proton and ammonium ions are obtained with ferric sulfate/ferrous sulfate as the redox couple. The formal transfer potentials and the standard Gibbs transfer energy of these ions are evaluated and consistent with the results obtained by a four-electrode system and other methods.

Investigation of proton transfer across the water/1,2-dichloroethane interface by o-phenanthroline using glass micro/nano-pipets and cyclic voltammetry

Facilitated proton transfer across the water/1,2-dichloroethane (DCE) interface supported on the tips of micro- and nano-pipets by o-phenanthroline (Phen) was studied by using cyclic voltammetry. The formed micro- and nano-liquid/liquid interfaces functioned as micro- and nano-electrodes under certain experimental conditions. The dependence of the half-wave potentials on the aqueous solutions acidities was studied and the ratio of association constants between Phen and proton in the aqueous and DCE phases was calculated by the method proposed by Matsuda et al.. The standard rate constant (k(0)) and the transfer coefficient (alpha) evaluated by using nano-pipets were equal to 0.183 +/- 0.054 cm/s and 0.70 +/- 0.09, respectively.