Trends in the solubility of iron,aluminium, manganese and phosphorus in aerosol collected over the Atlantic Ocean

The solubility of iron, aluminium, manganese and phosphorus has been determined in aerosol samples collected between 49°N and 52°S during three cruises conducted in the Atlantic Ocean as part of the European Union funded IRONAGES programme. Solubilities (defined at pH 4.7) determined for Fe and Al in samples of Saharan dust were significantly lower (medians 1.7% and 3.0%, respectively) than the solubilities of these metals in aerosols from other source regions (whole dataset medians 5.2% and 9.0%, respectively). Mn solubility also varied with aerosol source, but the median solubility of Mn in Saharan dust was very similar to the median for the dataset as a whole (55% and 56%, respectively). The observed solubility of aerosol P was ∼ 32%, with P solubility in Saharan aerosol perhaps as low as 10%. Laboratory studies have indicated that aerosol Fe solubility is enhanced by acid processing. No relationship could be found between Fe solubility and the concentrations of acid species (non-seasalt SO₄²⁻, NO₃⁻) nor the net acidity of the aerosol, so we are unable to confirm that this process is significant in the atmosphere. In terms of the supply of soluble Fe to oceanic ecosystems on a global scale, the observed higher solubility for Fe in non-Saharan aerosols is probably not significant because the Sahara is easily the dominant source of Fe to the Atlantic. On a smaller scale however, higher solubility for aerosol Fe may alter our understanding of Fe cycling in regions such as the remote Southern Ocean.     

济宁颜店铁矿地质特征及济宁岩群含矿性研究

伏于济宁滋阳山一带千米盖层之下的古元古代济宁岩群是一套低绿片岩相变质含铁岩系,主要岩石组合为千枚岩、板岩、磁铁石英岩等,其原岩为海相含灰质泥岩、砂岩类中酸性火山岩、硅铁岩等,该套岩系最大控制厚度达580m。其中赋存的条带状磁铁石英岩呈层状、似层状埋深在1612．89～1796．54m之间,共有5层铁矿,总厚度85．53m。估算预测的铁矿资源量（334）9．76亿t,mFe平均品位22．37％;低品位矿体预测的资源量（334）2．64亿t,mFe平均品位16．99％。     

Effects of irrigation on geochemical processes in a paddy soil and in ground waters in Camargue (France)

In waterlogged soils, dynamics of water influence the redox conditions and thus the mobility of elements. Irrigation of rice in Camargue (South eastern France) induces yearly dynamics of water. In order to determine the impact of irrigation on the geochemical properties of ground waters, a continuously in situ record of physico-chemical parameters (pH, Eh, temperature and electric conductivity) is performed during 1 year in an irrigated rice field. Seasonal dynamics show large Eh and pH variations. An annual irrigation cycle generates fast precipitations of Ca–Mg carbonates and Fe oxides between 50 and 110 cm depth when the soil is waterlogged. The dissolution of these minerals is initiated during a year without irrigation.     

Mais comment s'écoule donc un glacier ? Aperçu historique

Ice and snow have often helped physicists understand the world. On the contrary it has taken them a very long time to understand the flow of the glaciers. Naturalists only began to take an interest in glaciers at the beginning of the 19th century during the last phase of glacier advances. When the glacier flow from the upslope direction became obvious, it was then necessary to understand how it flowed. It was only in 1840, the year of the Antarctica ice sheet discovery by Dumont d'Urville, that two books laid the basis for the future field of glaciology: one by Agassiz on the ice age and glaciers, the other one by canon Rendu on glacier theory. During the 19th century, ice flow theories, adopted by most of the leading scientists, were based on melting/refreezing processes. Even though the word ‘fluid’ was first used in 1773 to describe ice, more the 130 years would have to go by before the laws of fluid mechanics were applied to ice. Even now, the parameter of Glen's law, which is used by glaciologists to model ice deformation, can take a very wide range of values, so that no unique ice flow law has yet been defined. To cite this article: F. Rémy, L. Testut, C. R. Geoscience 338 (2006).     

Origin of fluids in iron oxide–copper–gold deposits: constraints from δ 37Cl, 87Sr/86Sri and Cl/Br

The origin of the hypersaline fluids (magmatic or basinal brine?), associated with iron oxide (Cu–U–Au–REE) deposits, is controversial. We report the first chlorine and strontium isotope data combined with Cl/Br ratios of fluid inclusions from selected iron oxide–copper–gold (IOCG) deposits (Candelaria, Raúl–Condestable, Sossego), a deposit considered to represent a magmatic end member of the IOCG class of deposit (Gameleira), and a magnetite–apatite deposit (El Romeral) from South America. Our data indicate mixing of a high δ ³⁷Cl magmatic fluid with near 0‰ δ ³⁷Cl basinal brines in the Candelaria, Raúl–Condestable, and Sossego IOCG deposits and leaching of a few weight percent of evaporites by magmatic-hydrothermal (?) fluids at Gameleira and El Romeral. The Sr isotopic composition of the inclusion fluids of Candelaria, Raúl–Condestable, and El Romeral confirms the presence of a non-magmatic fluid component in these deposits. The heavy chlorine isotope signatures of fluids from the IOCG deposits (Candelaria, Raúl–Condestable, Sossego), reflecting the magmatic-hydrothermal component of these fluids, contrast with the near 0‰ δ ³⁷Cl values of porphyry copper fluids known from the literature. The heavy chlorine isotope compositions of fluids of the investigated IOCG deposits may indicate a prevailing mantle Cl component in contrast to porphyry copper fluids, an argument also supported by Os isotopes, or could result from differential Cl isotope fractionation processes (e.g. phase separation) in fluids of IOCG and porphyry Cu deposits.     

胃肠酸度下中药及补铁制剂中铁活性的影响研究

在人体胃肠液的酸度条件下,采用正辛醇-水分配体系模拟药物在人体肠胃中的分配情况,研究了中药和补铁制剂中铁的形态及其在人体内的吸收情况,并探讨了中药不同比例的配伍、胃肠酸度及还原性物质的存在对水溶态铁和醇溶态铁的影响。结果表明,药物溶液中的铁形态与药物本身特性和配伍情况有关,酸度及配伍对药物中铁的溶出率和溶液中铁的形态有较大影响,人体对铁的吸收与胃肠酸度和还原性物质的存在有关。     

磁铁石英岩型铁矿岩芯光谱编录研究

 对河北省昌黎县闫庄铁矿床的磁铁石英岩型铁矿石261件样品进行了光谱反射率测量，并与其铁含量进行了相关关系研究，目 的是对钻孔岩芯编录的新方法即高光谱岩芯编录在此类矿床中的可行性进行分析。研究结果表明，铁矿石反射率较低，一般为5%~20% ，铁离子的吸收峰主要表现在400~1 100 nm范围内，铁矿石中铁含量与850~900 nm的反射率均值呈现显著指数负相关关系，为高光谱 岩芯编录在此类矿床中的可行性提供了理论依据和技术途径。     

Tectonic setting and petrogenesis of the Çelebi granitoid, (Kırıkkale-Turkey) and comparison with world skarn granitoids

Many studies have shown systematic correlations between the composition of plutons worldwide and the metal content of associated skarns. This is the first report of similar correlations between the composition of Çelebi granitoid and skarns of the Çelebi district in Central Anatolia, Turkey. The Çelebi district is well known for its polymetallic Fe–W and Cu vein ores. These are hosted by calcic skarn zones. Both exoskarns (pyroxene–garnet) and endoskarns (epidote–pyroxene) occur in the district formed mainly along the granitoid contacts and along the fractures within the marble. Based on mineralogy, petrology and geochemistry, two different igneous rocks were recognized in the Çelebi granitoid, referred to as leucocratic (felsic) and mesocratic (intermediate) Çelebi granitoid. The leucocratic Çelebi occurs as dominant rock type, and is classified as granite. The mesocratic Çelebi is not widespread and is classified as adamellite, tonalite, quartz monzonite and quartz monzodiorite. The mesocratic Çelebi has I-type characteristics, and have subalkaline, calc-alkaline and metaluminous characteristics like most worldwide skarn granitoids.A post-collisional tectonic setting is proposed on the basis of field evidence, the relative timing of intrusions with respect to metamorphic and obducted ophiolitic rocks and trace element geochemistry. The high abundance of La and Ce and the enrichment of V in mafic components suggest that Çelebi granitoids are formed by partial melting of mantle rocks, but have been contaminated by interaction with continental crust involving possible magma mixing processes (i.e. mixing of coexisting felsic and mafic magmas). In the district, the mesocratic type and mafic microgranular enclaves (MME) mainly within leucocratic type represent a mafic underplating magma that was mixed with and/or injected into felsic magma of the leucocratic type.The present study shows that Fe mineralization is associated with mesocratic Çelebi type, whereas W mineralization is associated with leucocratic type. Mesocratic Çelebi granitoid is significantly different from the worldwide average of plutons associated with Fe skarns. In particular, MgO vs. SiO₂, FeOt+CaO+Na₂O/K₂O vs. SiO₂, Fe₂O₃/Fe₂O₃+FeO vs. SiO₂ and V vs. Ni vary from typical values (are lower than values typical for plutons associated with Fe skarns) for plutons associated with Fe skarns. Instead, it resembles the geochemical characteristics of plutons associated with worldwide Cu and possibly Au skarns. This suggests new exploration possibilities for copper and gold in the Çelebi district.     

Iron colloids/organic matter associated transport of major and trace elements in small boreal rivers and their estuaries (NW Russia)

The chemical status of major and trace elements (TE) in various boreal small rivers and watershed has been investigated along a 1500-km transect of NW Russia. Samples were filtered in the field through a progressively decreasing pore size (5, 0.8 and 0.22 μm; 100, 10, and 1 kD) using a frontal filtration technique. All major and trace elements and organic carbon (OC) were measured in filtrates and ultrafiltrates. Most rivers exhibit high concentration of dissolved iron (0.2–4 mg/l), OC (10–30 mg/l) and significant amounts of trace elements usually considered as immobile in weathering processes (Ti, Zr, Th, Al, Ga, Y, REE, V, Pb). In (ultra)filtrates, Fe and OC are poorly correlated: iron concentration gradually decreases upon filtration from 5 μm to 1 kD whereas the major part of OC is concentrated in the <1–10 kD fraction. This reveals the presence of two pools of colloids composed of organic-rich and Fe-rich particles. According to their behavior during filtration and association with these two types of colloids, three groups of elements can be distinguished: (i) species that are not affected by ultrafiltration and are present in the form of true dissolved inorganic species (Ca, Mg, Li, Na, K, Sr, Ba, Rb, Cs, Si, B, As, Sb, Mo) or weak organic complexes (Ca, Mg, Sr, Ba), (ii) elements present in the fraction smaller than 1–10 kD prone to form inorganic or organic complexes (Mn, Co, Ni, Zn, Cu, Cd, and, for some rivers, Pb, Cr, Y, HREE, U), and (iii) elements strongly associated with colloidal iron in all ultrafiltrates (P, Al, Ga, REE, Pb, V, Cr, W, Ti, Ge, Zr, Th, U). Based on size fractionation results and taking into account the nominal pore size for membranes, an estimation of the effective surface area of Fe colloids was performed. Although the total amount of available surface sites on iron colloids (i.e., 1–10 μM) is enough to accommodate the nanomolar concentrations of dissolved trace elements, very poor correlation between TE and surface sites concentrations was observed in filtrates and ultrafiltrates. This strongly suggests a preferential transport of TE as coprecipitates with iron oxy(hydr)oxides. These colloids can be formed on redox boundaries by precipitation of Fe(III) from inflowing Fe(II)/TE-rich anoxic ground waters when they meet well-oxygenated surface waters. Dissolved organic matter stabilizes these colloids and prevents their aggregation and coagulation. Estuarine behavior of several trace elements was studied for two small iron- and organic-rich rivers. While Si, Sr, Ba, Rb, and Cs show a clear conservative behavior during mixing of freshwaters with the White sea, Al, Pb and REE are scavenged with iron during coagulation of Fe hydroxide colloids.     

Iron(II) oxide determination in rocks and minerals

The determination of FeO of geologic materials by modern instrumental methods (such as atomic absorption spectroscopy (AAS), inductively coupled plasma atomic emission spectroscopy (ICP-AES), X-ray fluorescence (XRF), etc.) cannot distinguish between different oxidation states of elements. In many cases, the oxidation state of Fe has to be known in order to perform several chemical calculations (norms, etc.) and discuss the reactions that occur during weathering, hydrothermal alteration and other processes. A modified Wilson method is proposed, giving reproducible results in a much shorter time than the classical method. Back-titration with potassium dichromate and an Fe(II) and ammonia sulphate solution is used, after dissolution of the sample powder in a heated HF/H₃PO₄ mixture and an ammonium vanadate solution. This modified method, tested with several international reference materials, gives reliable results, equivalent to the ones cited in the literature for the reference materials.