Processes governing the carbon chemistry during the SAGE experiment

Measurements of pCO₂, pH and alkalinity in the surface waters of an iron fertilised patch of sub-Antarctic water were made during SAGE (SOLAS SAGE: Surface-Ocean Lower Atmosphere Studies Air-Sea Gas Experiment). The iron addition induced a minor phytoplankton bloom, however the patch dynamics were dominated by physical processes which suppressed and masked the biological effects. The Lagrangian nature of the experiment allowed the carbonate chemistry in the patch to be followed for 15.5 days, and the relative importance of the biological and physical factors influencing the surface water pCO₂ was estimated. The pCO₂ of the surface waters of the patch increased from 327 ??atm prior to iron addition to 338 ??atm on Day 14, effects of vertical and horizontal mixing offset the 15 ??atm drawdown that would have occurred had the induced biological uptake been the sole factor to influence the pCO₂. The air-sea carbon flux calculated using the measured skin temperature and a piston velocity parameterisation determined during SAGE (Ho et al., 2006) was 98.5% of the flux determined using conventional bulk temperature measurement and the Wanninkhof (1992) piston velocity parameterisation. The skin temperature alone contributed to an 8% increase in the flux compared with that determined using bulk temperature.     

Origin of iron and aluminium in large particles (> 53 µm) in the Crozet region, Southern Ocean

Natural iron fertilization processes are occurring around the Crozet Islands (46°26′S–52°18′E), thus relieving the water masses from the normally encountered High Nutrients Low Chlorophyll (HNLC) conditions of the Southern Ocean. During austral summers 2004/2005 and 2005/2006, iron and aluminium concentrations were investigated in large particles (> 53 µm) collected from just below the mixed layer at stations under the influence of island inputs, and also in adjacent HNLC waters. These large particles are anticipated to sink out of the mixed layer, and to reflect the net effects of input and cycling of these elements in the overlying mixed layer. Labile and refractory fractions were determined by a two-stage leaching technique. Data showed that water masses downstream of the islands were enriched in total iron and aluminium (0.25–2.68 nmol L^− 1 and 0.34–3.28 nmol L^− 1 respectively), relative to the southern HNLC control sites (0.15–0.29 nmol L^− 1 for Fe and 0.12–0.29 nmol L^− 1 for Al), with only a small fraction (typically < 1%) being acid leachable in both environments. Particulate iron predominantly derived from the island system represents a significant fraction of the total water column iron inventory and may complement dissolved Fe inputs that help support the high summer productivity around the Crozet islands.     

山东省东平汶上地区铁矿矿床成因探讨

山东省东平-汶上铁矿成矿带是鲁西重要的成矿带,区内已发现李官集、彭集等多个大中型铁矿床,探明了铁矿石资源量超过12亿t。通过收集东平-汶上地区基础地质调查、区域重磁、矿产勘查、科研成果等资料,分析了区内地层、构造、岩浆岩及区域航磁异常特征、重力异常特征与铁矿床的对应耦合关系,提出了矿床的3个控矿因素:即控矿地层(泰山岩群雁翎关组、山草峪组,地层控矿专属性)、控矿构造(同斜复式背斜构造)、控矿岩浆岩(改造和破坏了铁矿带的完整性),通过对成矿区带样品采集测试,分别从主量元素、稀土元素、微量元素、原岩恢复、变质岩构造背景等方面进行系统分析对比,探讨了该区铁矿床为海相岛弧火山——沉积变质成因。     

Iron speciation and biogeochemistry in different nearshore waters

Different environmental conditions in various nearshore waters dynamically determine the speciation of iron, its solubility, removal and hence bioavailability to phytoplankton. The iron speciation, the impact of phytoplankton blooms and the effects of organic matter on iron speciation and transformation were studied in four different coastal systems: the Trondheim Fjord, Norway, which is a coastal system that is open to a vast riverine impact; Hopevågen, Norway, a pristine coastal basin, which has negligible river and anthropogenic impact; zmir Bay, Turkey, a Mediterranean embayment with heavily polluted eutrophic inner–middle section, and the oligotrophic outer section. In this paper, we compare iron speciation in these different coastal systems. While colloidal iron (ColFe) was the predominant species especially in the Trondheim Fjord and to some degree also in Hopavågen, Chelex labile iron (ClxLFe) and hydrophobic organic-iron complex (HpOFe) were predominate species in both the inner–middle and the outer section of zmir Bay. The impact of phytoplankton blooms on the ClxLFe was significant especially in the Trondheim Fjord, in the inner–middle section of zmir Bay and in Hopevågen.     

秘鲁南部Morrito铁矿矿体变化程度分析

Morrito铁矿严格受断裂构造控制,在空间上的厚度、品位有较大变化。利用统计学的方法,研究了矿脉厚度、品位的变化系数,对矿体的资源/储量估算及开采都有重要意义。对矿体厚度及品位变化系数的分析认为,矿体形态变化程度属"简单";矿体有用组分分布属"均匀";矿体倾向变化大于走向变化,并表现为不明显的方向性变化。     

Uranium isotopic evidence for the origin of the Bahariya iron deposits, Egypt

The economic iron ore deposits of Egypt are located at Bahariya Oasis in the Lower Middle Eocene limestone. The main iron minerals are goethite, hematite, siderite, pyrite, and jarosite. Manganese minerals are pyrolusite and manganite. Gangue minerals are barite, glauconite, gibbsite, alunite, quartz, halite, kaolinite, illite, smectite, palygorskite, and halloysite. Geochemical comparison between the ore and the Nubia sandstone showed that the ore is depleted in the residual elements (Al, Ti, V, and Ni) and enriched in the mobile elements (Fe, Mn, Zn, Ba, and U) which indicates that the Bahariya iron ore is not a lateritic deposit despite the deep weathering in this area. On the other hand, the Nubia sandstone showed depletion in the mobile elements, which demonstrates the leaching process in the Nubia Aquifer. The presence of such indicator minerals as jarosite, alunite, glauconite, gibbsite, palygorskite, and halloysite indicate that the ore was deposited under strong acidic conditions in fresh water.Isotopic analyses of the uranium in the amorphous and crystalline phases of the ore, in the country rocks, and dissolved in the Nubia Aquifer water, all support the conclusion that U and Fe were precipitated together from warm ascending groundwater. U and Fe display strong co-variation in the ore, and the ²³⁴U/²³⁸U activity ratio of the newly precipitated U in the country rock and the leached component of U in the groundwater are identical. There is only slightly more uranium in the amorphous phase than in the crystalline and only a slightly lower ²³⁴U/²³⁸U activity ratio, suggesting that the iron in the two phases have a similar origin. Comparison of the excess ²³⁴U in the water and in the total ore leads to the conclusion that the precipitation of the U, and by inference the iron, occurred within the last million years. However, that both precipitation and leaching of U have occurred over the last 300,000 years is evidenced by the extreme ²³⁰Th/²³⁴U disequilibria observed in some of the samples. Some of the amorphous depositional events have been very recent, perhaps within the last 10,000 years.     

Bacterial iron oxide reduction in a terrigenous sediment-impacted tropical shallow marine carbonate system, north Jamaica

Discovery Bay, a carbonate-dominated embayment in north Jamaica, has been subject to inputs for 40 years of iron-rich bauxite sediment associated with the local mining and transport of processed bauxite. As such, this site is an ideal natural laboratory to study the records and impacts of iron oxide inputs upon geochemical, diagenetic, and microbial processes in tropical carbonate sediments.Total Fe contents in sites in the bay not receiving bauxite inputs are negligible and porewater Ca²⁺, SO₄²⁻ and Cl⁻ indicate that bacterial sulphate reduction is an important process. In contrast, surface sediments receiving bauxite inputs contain significant total Fe, from 44 μmol/g in shallow (5 m water depth) sites to 110 μmol/g in deeper (20 m water depth) sites. Up-core increases in total Fe record increased temporal inputs into the bay. Within these Fe-rich sediments porewater data shows the presence of Fe^II released by bacterial Fe^III reduction. There is no direct evidence for significant bacterial sulphate reduction in these sediments. Iron oxides within all bauxite-impacted sediments display a high potential reducibility, from 40% to 80% of the total Fe present as dithionite-extractable Fe^III. Experimental analysis of the potential susceptibility to, and rates of, bacterial Fe^III reduction, utilising Discovery Bay sediment and Shewanella putrefaciens CN32 (a known Fe^III-reducer) has confirmed the high bacterial reducibility of iron oxides within the sediment. Up to 75% of initial dithionite-extractable Fe^III in the sediments was reduced over 15 days.The presence of iron oxides within the Discovery Bay shallow marine carbonate systems has markedly altered the chemical diagenetic processes taking place, with a shift from apparent dominance of bacterial sulphate reduction at non-impacted (Fe-poor) sites, to highly significant bacterial Fe^III reduction in Fe-rich bauxite-impacted sediments. Given the perceived global increases in terrigenoclastic sediment inputs into tropical carbonate systems as a result of land-use and climate changes, coupled with the documented role that iron oxide reduction plays in nutrient and contaminant cycling in sediment systems, more research into the perturbation of early diagenesis by iron oxide inputs is required.     

Enhancing the Sustainability of Household Fe0/Sand Filters by Using Bimetallics and MnO2

Filtration systems containing metallic iron as reactive medium (Fe⁰ beds) have been intensively used for water treatment during the last two decades. The sustainability of Fe⁰ beds is severely confined by two major factors: (i) reactivity loss as result of the formation of an oxide scale on Fe⁰ and (ii) permeability loss due to pore filling by generated iron corrosion products. Both factors are inherent to iron corrosion at pH > 4.5 and are common during the lifespan of a Fe⁰ bed. It is of great practical significance to improve the performance of Fe⁰ beds by properly addressing these key factors. Recent studies have shown that both reactivity loss and permeability loss could be addressed by mixing Fe⁰ and inert materials. For a non‐porous additive like quartz, the threshold value for the Fe⁰ volumetric proportion is 51%. Using the Fe⁰/quartz system as reference, this study theoretically discusses the possibility of (i) replacing Fe⁰ by bimetallic systems (e.g., Fe⁰/Cu⁰), or (ii) partially replacing quartz by a reactive metal oxide (MnO₂ or TiO₂) to improve the efficiency of Fe⁰ beds. Results confirmed the suitability of both tools for sustaining Fe⁰ bed performance. It is shown that using a Fe⁰:MnO₂ system with the volumetric proportion 51:49 will yield a filter with 40% residual porosity at Fe⁰ depletion (MnO₂ porosity 62%). This study improves Fe⁰ bed design and can be considered as a basis for further refinement and detailed research for efficient Fe⁰ filters.     

Optical properties and light penetration in a deep,naturally acidic,iron rich lake: Lago Caviahue (Patagonia,Argentina)

The optical properties and light climate in the deep and extremely acid Lake Caviahue have been studied in order to better understand its characteristics and the possible influence upon the phytoplankton community. The absorption coefficients for the dissolved fraction were maximal in the ultraviolet (UV) region and the water absorption spectra showed a shoulder around 300 nm, which was attributed to the concentration of Fe(III). No radiation was detected in the water column below 360 nm. The depth of the 1% incident radiation was dependent of wavelength, showing its maximum of 13.3 m at 565 nm, compared to 1.7 m and 4.8 m at 400 nm and 700 nm, respectively. Phytoplankton biomass was low and showed an almost constant profile with depth despite the relative darkness of the water column. Optical climate of Lake Caviahue is not typical of high elevation lakes but is more similar to low elevation shallow lakes of the Andean region. The chemical composition of the water, mainly Fe oxidation state and concentration, is the responsible for the high attenuation of the UV radiation (UVR). Living organisms are protected of UVR because Lake Caviahue waters are a shield against UV-B.