长江口沉积物-水界面砷的迁移转化机制与微生物调控分析

为探析长江口沉积物-水界面砷的迁移转化机制,本文分析了2019年夏季长江口4个站位上覆水和间隙水中总As浓度及形态的剖面变化特征,耦合氧化还原敏感元素(Fe、Mn和S)的剖面变化剖析了沉积物-水界面砷循环的Fe-Mn-S控制机制,同时结合砷相关功能基因探讨了沉积物-水界面砷迁移转化的微生物调控过程,估算了沉积物-水界面总As的扩散通量。结果表明,除A7-4站位外,长江口其他3个站位间隙水总As以As³⁺为主要存在形态,且总As浓度均在上覆水中为最低值(0.748~1.57 μg·L^-1),而在间隙水中随着深度增加而逐渐增加并在6~9 cm深度达到峰值(7.14~26.9 μg·L^-1)。间隙水总As及As³⁺浓度的剖面变化趋势与溶解态Fe²⁺、Mn²⁺相似,其均在中间层出现高值,说明沉积物Fe/Mn还原带砷的释放可能是随固相Fe(Ⅲ)或Mn(Ⅳ)的还原而转移到间隙水中的。氧化层和Fe/Mn还原带过渡区间隙水砷浓度与砷异化还原菌功能基因arrA和arsC丰度存在对应关系(除A1-3站外),说明砷异化还原菌将溶解As⁵⁺或固相As⁵⁺还原为溶解As³⁺可能是该过渡层砷迁移转化的另一重要过程。硫酸盐还原带的间隙水总As和As³⁺浓度降低,但由于间隙水的低S^2-浓度不利于砷硫化物生成,因此深层间隙水砷可能与铁硫矿物结合而被移除。底层环境氧化还原条件是影响沉积物-水界面砷迁移转化的重要因素,随底层水DO浓度的降低,砷迁移转化更倾向于微生物还原控制。长江口沉积物-水界面总As的扩散通量为1.18×10^-7~2.07×10^-7 μmol·cm^-2·s^-1,均表现为沉积物间隙水中总As向上覆水释放,即沉积物是研究区域水体总As的来源之一。     

Long‐term annual surface heat and water balances over Canada and the United States South of 60°N: Reconciliation of precipitation,run‐off and temperature fields

Abstract

The analysis compares the observed field of run‐off (assumed correct) with adjusted precipitation over North America (as amended by den Hartog and LeDrew over Canada) and derives the principal hydroclimatological ratios for each five‐degree latitude‐longitude square. The amended precipitation field yields values of the Budyko dry ness index close to values suggested by the vegetation distribution. The Priestley‐Taylor parameter, α, lies between unity (equilibrium) and potential (1.26) values over much of humid North America, but exceeds these values in the northwest Pacific squares, where advective heating may be the cause. Other regions of strong seasonal advective heating (e.g. the Great Plains) do not appear to influence the distribution strongly. A weighted convective forcing temperature is derived, varying from 298 K in the extreme south to below 285 K in the north. This function (and the Bowen ratio) achieve improbable values in northern Labrador‐ Ungava. The precipitation, run‐off and net radiation régimes appear still to be out of balance in these squares. An adjustment of either precipitation or net radiation by about a tenth corrects the imbalance, but the method is not capable of deciding which field (or both) is in error. Over the rest of the continent the adjusted precipitation field now appears to be in balance with observed run‐off and temperature distributions.     

中天山坡地冰缘地貌的若干问题

由 1985—1989年野外调查结果和定位重复观测资料可知,本区坡地冰缘地貌的分布特征为:1.各类坡地冰缘形态彼此具有成因联系;2.不同序次的冰缘地貌类型具有各自的时空分异;3.不同的坡地冰缘地貌类型在一定条件下可有所转化。再则,本区风化以寒冻剥裂和寒冻楔入为主,呈现在时空和状态上为不可逆过程的耗散结构。     

Calibration method affects the measured δ2H and δ18O in soil water by direct H2Oliquid–H2Ovapour equilibration with laser spectroscopy

The direct H₂O_liquid–H₂O_vapour equilibration method utilizing laser spectroscopy (DVE-LS) is a way to measure soil pore water stable isotopes. Various equilibration times and calibration methods have been used in DVE-LS. Yet little is known about their effects on the accuracy of the obtained isotope values. The objective of this study was to evaluate how equilibration time and calibration methods affect the accuracy of DVE-LS. We did both spiking and field soil experiments. For the spiking experiment, we applied DVE-LS to four soils of different textures, each of which was subjected to five water contents and six equilibration times. For the field soil experiment, we applied three calibration methods for DVE-LS to two field soil profiles, and the results were compared with cryogenic vacuum distillation (CVD)-LS. Results showed that DVE-LS demonstrated higher δ²H and δ¹⁸O as equilibration time increased, but 12 to 24 hr could be used as optimal equilibration time. For field soil samples, DVE-LS with liquid waters as standards led to significantly higher δ²H and δ¹⁸O than CVD-LS, with root mean square error (RMSE) of 8.06‰ for δ²H and 0.98‰ for δ¹⁸O. Calibration with soil texture reduced RMSE to 3.53‰ and 0.72‰ for δ²H and δ¹⁸O, respectively. Further, calibration with both soil texture and water content decreased RMSE to 3.10‰ for δ²H and 0.73‰ for δ¹⁸O. Our findings conclude that the calibration method applied may affect the measured soil water isotope values from DVE-LS.     

Evaluation of the Bioavailability of Metals in Sediment from the Southern Coastal Wetland of the Qiantang Estuary by Using Diffusive Gradients in Thin Films Technique

Metal pollution has become an major issue governing the wetland ecosystem health.The southern coastal wetland of the Qiangtang Estuary are facing unusual perturbation due to rapid development along the embayment in recent decades.This study evaluated the bioavailability of metals(Cu,Pb,Cd,Cr and Zn)in the sediment of the southern coastal wetland of the Qiangtang Es-tuary using diffusive gradients in thin films(DGT)techniques and compared with several methods based on total metal content.The results showed that the contents of Cr,Pb,Cd and Cu in sediment,as detected using DGT,were considerably correlated with the exchangeable fraction and the content in Phragmites australis roots,while a weak correlation was observed for Zn.Therefore,DGT analysis could be used to evaluate the bioavailability and potential risk of Cr,Cd,Pb and Cu for P.australis.Quantitative indices,such as DGT concentration,bioaccumulation in P.australis,geoaccumulation index(Igeo)and potential ecological risk index(RI),revealed that Cd was a major potential ecological risk factor along the southern coast wetland of the Qiantang Estuary,especially in the upstream region,which is potentially more vulnerable to the anthropogenic pollution.     

长江中下游典型浅水湖泊沉积物水界面磷与铁的耦合关系

目前普遍认为磷铁耦合关系是P迁移的主要机制,但大部分研究结果并未提供直接的原位证据.为了探索沉积物剖面磷(P)与铁(Fe)的耦合关系,利用Zr O-Chelex薄膜扩散梯度技术(ZrO-Chelex DGT),分别对太湖、巢湖、鄱阳湖和洞庭湖4个浅水湖泊沉积物有效态Fe和P进行高分辨采样和分析.结果表明,不同湖区有效态Fe和P浓度在沉积物-水界面处开始增加,之后波动变化,垂向异质性较强,但两者浓度变化同步.有效态P和Fe浓度的相关分析结果证明两者浓度具有显著的线性相关.室内厌氧培养实验进一步表明,Fe~(3+)的还原性促使Fe~(2+)与铁结合态磷的释放,促使DGT有效态P与Fe同步变化.该结果表明沉积物P的二次迁移和释放受Fe氧化还原过程的控制,为铁磷耦合关系提供了直接证据.     

Generalized flux law,with an application

A generalized flux law, which can specialize into power‐ and diffusive‐type flux laws, is proposed. When coupled with the continuity equation, a generalized flow equation is the result. The generalized equation specializes into several cases, one of which is the kinematic wave equation. By applying the generalized flow equation and its variants to flow routing in two rivers, the usefulness of the generalized flux law is evaluated. Copyright © 1999 John Wiley & Sons, Ltd.     

Macrodynamics of α2 dynamos

Abstract

Two distributions of the α-effect in a sphere are considered. The inviscid limit is approached both by direct numerical solution and by solution of a simpler nonlinear eigenvalue problem deriving from asymptotic boundary layer analysis for the case of stress-free boundaries. The inviscid limit in both cases is dominated by the need to satisfy the Taylor constraint which states that the integral of the Lorentz force over cylindrical (geostrophic) contours in a homogeneous fluid must tend to zero. For a small supercritical range in α, this condition can only be met by magnetic fields which vanish as the viscosity goes to zero. In this range, the agreement of the two approaches is excellent. In a portion of this range, the method of finite amplitude perturbation expansion is useful, and serves as a guide for understanding the numerical results. For larger α, evidence from the nonlinear eigenvalue problem suggests both that the Taylor state exists, and that the transition from small to large amplitude can require a finite amplitude (oscillatory) instability in accord with the findings of Soward and Jones (1983). However, solutions of the full equations have not been found which are independent of viscosity at larger values of α.     

Petrology and geothermometry of retrograded Hercynian charnockites and host gneisses, Agly Massif, French Pyrenees

Abstract A Hercynian charnockite occurs within high-grade gneisses in the Agly Massif, French Pyrenees. Its thermal history has been evaluated using the Fe-Mg distribution coefticient ( K _D) between garnet and biotite. These minerals have different origins but similar compositions in the charnockites and host gneisses. In the charnockite, the Bi–Ga pairs are the retrograde products of Opx alteration. This Opx reaction with feldspar can be written. Opx + PI + Fluid 1(H₂O + Al + K + Fe + Ti) = Bi + Ga + Q + Fluid 2(H₂O + Na). The garnets are relatively Ca poor (4–2.5% grossular); they are automorphic and zoned in the gneisses and poikiloblastic in the charnockites. Both types show a retrograde rim (of few hundred microns'width) across which Fe and Mn increase as Mg decreases. The biotites show a good correlation between the octahedral cations (Ti⁴⁺+ Fe²⁺) and (Mg²⁺+ Al³⁺_VI); Ti and Fe both increase, whereas Mg and Al_VI decrease. There is an inverse linear correlation between Fe²⁺ and Mg²⁺ and the Fe/Mg ratio increases as Ti increases. The relation between Ti and K ^Ga-Bi_DFe-Mg is less clear: it seems that K _D slightly decreases as Ti increases. The equilibration temperatures of Ga–Bi pairs are discussed: the charnockite Ga-Bi pairs have equilibrated between 550°C and 600°C; whereas those of the gneisses have equilibrated between 550°C and 650°C. Two main thermal steps appear: one in the gneisses between 600-650°C and a second one in both the gneisses and the charnockites between 550°C and 600°C.     

Tidal time-scale variation in nutrient flux across the sediment–water interface of an estuarine tidal flat

We determined the range of the tidal variations in nutrient flux across the sediment–water interface and elucidated mechanisms of the flux variation in two estuarine intertidal flats (one sand, one mud) in northeastern Japan. Nutrient flux was measured using in situ light and dark chambers, which were incubated for 2 h, 2–6 times per day. Results showed that nutrient concentration in overlying water varied by tide and was also affected by sewage-treated water inflow. The nutrient fluxes responded quickly to the tidal variation in overlying water chemistry and the range of the variation in flux was as large as the seasonal-scale variation reported in previous studies. In the sand flat, salinity increase likely enhanced benthos respiration and led to increases in both O₂ consumption and PO₄³⁻ regeneration under low illumination, while benthic microalgae were likely to actively generate O₂, uptake PO₄³⁻ and suppress PO₄³⁻ release under high illumination (>900 μmol photons m⁻² s⁻¹). Also in the mud flat, PO₄³⁻ flux was related with O₂ flux, although the range of temporal variation in PO₄³⁻ flux was small. In both the flats, NH₄⁺ flux was always governed by NH₄⁺ concentration in the overlying water; either an increase in NH₄⁺ uptake or a decrease in NH₄⁺ release was observed as the NH₄⁺ concentration rose due to inflow of river water or input of sewage-treated water. Although NO₃⁻ tended to be released in both tidal flats when low NO₃⁻ concentration seawater dominated, their relationship was likely to be weakened under conditions of low oxygen consumption and suppressed denitrification. It is likely that tidal variation in nutrient flux is governed more by the nutrient concentration than other factors, such as benthic biological processes, particularly in the case where nutrient concentration in the overlying water is relatively high and with wide amplitude.