Iodine chemistry in deep anoxic basins and overlying waters of the Mediterranean Sea

Iodate (IO₃⁻) is the predominant dissolved species of iodine in the oxygenated waters of the Mediterranean Sea. Iodide (I⁻) is present in significant quantities (up to 65 nM) in oxygenated waters in the photic zone and near the interface above the anoxic and saline Bannock Basin. Lesser quantities of I⁻ (< 10 nM) are found throughout the rest of the oxic water column. An additional unidentified dissolved iodine species is present immediately above the anoxic interface.Total dissolved iodine (ΣI) increases dramatically across the seawater/brine interface. Part of this increase is undoubtedly the result of the dissolution of iodine-rich evaporites during formation of the brine bodies at the Tyro and Bannock Basins. The vertical distribution of ΣI and other dissolved chemical species (particularly PO₄³⁻) in the Bannock Basin brine, however, suggests an additional, present-day, diagenetic source of dissolved iodine to the brine. Based on the increase in the concentration of the most soluble major ions across the seawater/brine interface, 5–7 μM of the 11.5-μM increase in ΣI concentration must be attributed to diagenesis.     

Eddy correlation measurements of methane flux in a northern peatland ecosystem

A pilot study to measure methane flux using eddy correlation sensors was conducted in a peatland ecosystem in north central Minnesota. A prototype tunable diode laser spectrometer system was employed to measure the fluctuations in methane concentration.The logarithmic cospectrum of methane concentration and vertical wind velocity fluctuations under moderately unstable conditions had a peak nearf = 0.10 (wheref is the nondimensional frequency) and was quite similar to the cospectra of water vapor and sensible heat. Daytime methane flux during the first two weeks of August ranged from 120 to 270 mg m^-2 day^-1. The temporal variation in methane fluxes was consistent with changes in peat temperature and water table elevation. Our results compared well with the range of values obtained in previous studies in Minnesota peatlands.These field observations demonstrate the utility of the micrometeorological eddy correlation technique for measuring surface fluxes of methane. The current state-of-the-art in tunable diode laser spectroscopy makes this approach practical for use in key ecosystems.Published as Paper No. 9556, Journal Series, Nebraska Agricultural Research Division.     

Dissolved iodine flux from estuarine sediments and implications for the enrichment of iodine at the sediment water interface

During the anaerobic decomposition of organic matter in sediments iodine is released into solution. Three techniques have been applied to independently estimate the resulting flux of soluble I from the sediments to the overlying water of Mud Bay, Georgetown, South Carolina. Flux estimates (summer) range between ~ 5 and 41 μmol/m²/day. The estimates predicted from either the pore water I concentration gradient across the sediment-water interface or the dissolved I production rate are higher than the apparent flux measured directly at the same site. This suggests that I which is released to the pore water under the anoxic conditions below the sediment surface reacts with a sedimentary component at or near the sediment water interface and is lost from solution.     

Rates of iodine remineralization in terrigenous near-shore sediments

Much of the sedimentary geochemistry of iodine has been surmised from analyses of solid phase distributions without direct documentation of reactions or reaction rates. It is shown here that the anoxic production rate of dissolved I in nearshore terrigenous sediments decreases rapidly below the sediment-water interface and is strongly temperature controlled. An apparent activation energy of ~19.3 Kcal/mole comparable to that found for other microbially mediated reactions, describes the temperature dependence of release. Production of dissolved iodide is zeroth order with respect to natural ranges of pore water concentrations and apparently first-order with respect to a reactive I component in the solid phase. First order reaction coefficients in sediments from Mud Bay, South Carolina and Long Island Sound, Connecticut, U.S.A., are strongly depth dependent, varying from ~6.9/yr in the top few centimeters to an average of ~0.011/yr over the upper 70 cm. About 90% of the dissolved I flux comes from the top 10 cm with estimated values of ~ 15 and 29 μmoles/m²/day at 22–23°C in Mud Bay and Long Island Sound, respectively. The I/C net release ratio of decomposing material changes rapidly below the sediment surface. When temperature corrections are made, I remineralization rates from nearshore sediments below the bioturbated zone appear to be similar to those observed in deep water sediments underlying oxygenated waters.     

SeaSonde Radial Velocities: Derivation and Internal Consistency

This paper describes the methods presently used to produce unaveraged radial velocity maps from radar voltage cross spectra measured by a SeaSonde, including a discussion of the multiple signal classification (MUSIC) algorithm as it is applied to SeaSonde data and methods employed to alleviate difficulties associated with the use of measured antenna patterns. We also describe internal consistency checks including visual observation of the radial velocity map, consideration of the computed uncertainties and quantitative tests of radial velocities measured by two radars along the baseline between the systems. Baseline analysis is illustrated by application to two SeaSonde networks, with contrasting results that lead to a better understanding of SeaSonde output     

Simulated impacts of artificial groundwater recharge and discharge on the source area and source volume of an Atlantic Coastal Plain stream, Delaware, USA

A numerical groundwater-flow model was used to characterize the source area and volume of Phillips Branch, a baseflow-dominated stream incising a highly permeable unconfined aquifer on the low relief Delmarva Peninsula, USA. Particle-tracking analyses indicate that the source area (5.51 km²) is ～20% smaller than the topographically defined watershed (6.85 km²), and recharge entering ～37% of the surface watershed does not discharge to Phillips Branch. Groundwater residence time within the source volume ranges from a few days to almost 100 years, with 95% of the volume “flushing” within 50 years. Artificial discharge from groundwater pumping alters the shape of the source area and reduces baseflow due to the interception of stream flow paths, but has limited impacts on the residence time of groundwater discharged as baseflow. In contrast, artificial recharge from land-based wastewater disposal substantially reduces the source area, lowers the range in residence time due to the elimination of older flow paths to the stream, and leads to increased discharge to adjacent surface-water bodies. This research suggests that, in this and similar hydrogeologic settings, the “watershed” approach to water-resource management may be limited, particularly where anthropogenic stresses alter the transport of soluble contaminants through highly permeable unconfined aquifers.     

Dissolved nutrient fluxes through a sandy estuarine beachface (Cape Henlopen,Delaware, U.S.A.): Contributions from fresh groundwater discharge,seawater recycling,and diagenesis

The sandy beachface at Cape Henlopen, Delaware, receives dissolved nutrient inputs from fresh upland groundwater and estuarine seawater and exports nutrients through intertidal and submarine groundwater discharge. The discharge of brackish beachface waters indicates that there must be additional diagenetic nutrient sources and sinks within the porous beachface aquifer. At some times of the year, diagenetic processes within the beachface remove nitrate from waters draining the beachface consistent with the stoichiometry of either denitrification or dissimilatory nitrate reduction to ammonium. Up to 50–100% of the nitrate load from the upland groundwaters is apparently reduced to N₂O/N₂ gas or ammonium during these periods. At other times, ammonium and nitrate are added to beachface waters consistent with the stoichiometry of organic matter remineralization and nitrification. Dissolved reactive phosphorus and silica are similarly consumed and produced by beachface processes at different times of the year, presumably by adsorption or desorption. Infiltration of reactive estuarine particles may be an additional source of nutrients and carbon that supports the diagenetic activity in the beachface aquifer. These observations suggest that sandy beachfaces are biogeochemically reactive systems that can serve as sources, sinks, and temporary reservoirs of nutrients to support the primary and secondary production of the adjacent intertidal zone.     

再论花岗岩按照Sr-Yb的分类:标志

2006年作者曾经按照Sr=400×10~(-6)和Yb=2×10~(-6)作为标志将花岗岩分为埃达克岩、喜马拉雅型花岗岩、浙闽型花岗岩和广西型花岗岩,在浙闽型中又分出南岭型(Sr100×10~(-6)和Yb2×10~(-6)),于是花岗岩被分为5类。Sr=400×10~(-6)和Yb=2×10~(-6)是根据阿留申群岛中的Adak岛的资料得出来的。本文统计了全球花岗岩6000多个数据(其中,埃达克型花岗岩为2810个,喜马拉雅型花岗岩636个,浙闽型花岗岩1183个,南岭型花岗岩1518个,广西型花岗岩142个,总共6289个),统计的结果,各类花岗岩的地球化学特征大致如下:(1)埃达克型花岗岩富Al_2O_3和Sr,贫Y和Yb,具较高和变化的铕异常,绝大多数样品的Sr300×10~(-6),Yb2.5×10~(-6)(当Sr=400×10~(-6)～600×10~(-6)时Yb值最大,Sr超过600×10~(-6),Yb降低至2×10~(-6)),Al_2O_3在14%～18%之间,Eu/Eu~*大多在0.6～1.2范围;(2)喜马拉雅型花岗岩贫Sr和Yb,具中等的Al_2O_3和变化的Eu/Eu~*,Sr300×10~(-6)和Yb2×10~(-6)(少数Sr300×10~(-6)),Al_2O_3为13%～17%,Eu/Eu~*为0.2～1.0;(3)浙闽型花岗岩贫Sr富Yb,Sr在40×10~(-6)～400×10~(-6)之间,Yb1.5×10~(-6),Al_2O_3和Eu/Eu~*的变化类似喜马拉雅型花岗岩,Al_2O_3为12%～17%,Eu/Eu~*为0.4～1.0;(4)南岭型花岗岩以很低的Sr、Al_2O_3和Eu/Eu~*以及很高的Yb而不同于上述各类花岗岩,通常Yb1.5×10~(-6),Sr100×10~(-6)(Yb变化大,绝大多数2×10~(-6);当Yb在2×10~(-6)～8×10~(-6)时,部分样品Sr可100×10~(-6),但很少200×10~(-6));Al_2O_314%,集中在11%～13%之间,Eu/Eu~*0.7,大多0.4;Yb越大,Sr越低,负铕异常越明显。文中讨论了花岗岩Sr-Yb分类的意义,指出本分类适用于产于大陆和海洋的绝大多数中酸性岩浆岩(可能不适用于一部分特别富铁和钾的花岗岩,如具有高Sr和Yb特征的广西型花岗岩)。不同类型的花岗岩主要反映了源区压力的不同,而源区成分、温度、部分熔融程度、水和挥发分的加入以及岩浆混合等的影响可能是次要的。文中指出,该分类的依据、其实质,是熔体与残留相平衡的理论。与浙闽型花岗岩平衡的残留相是斜长石,与喜马拉雅型花岗岩平衡的是斜长石+石榴石,与埃达克型花岗岩平衡的是石榴石,与南岭型花岗岩平衡的是富钙的斜长石。文中指出,加强实验岩石学研究,将年代学和地球化学研究密切结合起来是深化花岗岩研究的关键。     

内蒙古西拉沐伦成矿带碾子沟钼矿床成矿流体地球化学特征

碾子沟钼矿床是内蒙古西拉沐伦钼多金属成矿带中石英脉型钼矿床的典型代表,矿体以石英大脉形式产于燕山期中粗粒黑云母二长花岗岩内,受断裂构造控制。流体包裹体研究发现包裹体均为气液两相,按照相比不同,可进一步分为WL型(5%～20%)和WV型(20%～50%)。Ⅰ阶段流体为低温(89.3～245.2℃)、中低盐度(2.07%～17.96%NaCleqv)流体;Ⅱ阶段流体具有中低温(134.4～458.8℃,峰值170℃～240℃)、中低盐度(0.53%～19.92%NaCleqv)特征;Ⅲ阶段流体为低温(134.9～202.4℃)、中低盐度(4.96%～14.97%NaCleqv)流体。流体成分均以H2O为主(96.1mol%),含少量挥发份CO2、N2、CH4、C2H6、Ar、H2S,阳离子以Na+为主,阴离子以SO42-、Cl-为主,属NaCl-H2O体系。各阶段成矿热液氢、氧同位素特征为:δ18OH2O介于-5.75‰～-1.90‰、δD介于-128.821‰～-109.234‰,说明成矿流体是岩浆热液与古大气降水混合而成。开放的断裂体系为流体混合创造了条件,流体的混合作用是造成碾子沟辉钼矿沉淀成矿的主要原因。这与斑岩型钼矿床的高盐度流体以及以沸腾为主的矿石沉淀机制具有显著区别。