Magnetic cleansing of weathered/tarry oiled feathers--the role of pre-conditioners

Iron powder has previously been demonstrated to be effective in the removal, via magnetic harvesting, of a wide variety of oil contaminants from feathers and plumage. This study investigates the efficacy of magnetic cleansing for the removal from feathers of tarry contamination that has been allowed to weather. Clusters of feathers from Mallard duck (Anas platyrhnchos) and Little Penguin (Eudyptula minor) were completely immersed in a tarry contaminant and allowed to weather from one to fourteen days. The contaminant was removed using a magnetic cleansing protocol and the removal efficacy assessed gravimetrically. For one, seven and fourteen days of weathering, a final removal (after fourteen treatments) of more than 99% and 97% was achieved for duck feathers and penguin feathers, respectively. Repeating the experiments (for a seven-day weathering period) for both duck and penguin feathers, with the judicious application of a pre-conditioner (olive oil), further improved removal efficacy. A convenient method to screen for improved pre-conditioning agents is suggested.     

Constraining models of the tectonic setting of the giant Olympic Dam iron oxide–copper–gold deposit, South Australia, using deep seismic reflection data

In the Gawler Craton, the completeness of cover concealing the crystalline basement in the region of the giant Olympic Dam Cu–Au deposit has impeded any sufficient understanding of the crustal architecture and tectonic setting of its IOCG mineral-system. To circumvent this problem, deep seismic reflection data were recently acquired from  250 line-km of two intersecting traverses, centered on the Olympic Dam deposit. The data were recorded to 18 s TWT ( 55 km). The crust consists of Neoproterozoic cover, in places more than 5 km thick, over crystalline basement with the Moho at depths of 13–14 s TWT ( 40–42 km). The Olympic Dam deposit lies on the boundary between two distinct pieces of crust, one interpreted as the Archean–Paleoproterozoic core to the craton, the other as a Meso–Neoproterozoic mobile belt. The host to the deposit, a member of the  1590 Ma Hiltaba Suite of granites, is situated above a zone of reduced impedance contrast in the lower crust, which we interpret to be source-region for its  1000 °C magma. The crystalline basement is dominated by thrusts. This contrasts with widely held models for the tectonic setting of Olympic Dam, which predict extension associated with heat from the mantle producing the high temperatures required to generate the Hiltaba Suite granites implicated in mineralization. We use the seismic data to test four hypotheses for this heat-source: mantle underplating, a mantle-plume, lithospheric extension, and radioactive heating in the lower crust. We reject the first three hypotheses. The data cannot be used to reject or confirm the fourth hypothesis.     

A geographical analysis of the Atalanti alluvial plain and coastline as the location of a potential tourist site, Bronze through Early Iron Age Mitrou, East-Central Greece

Tourism accounts for 15% of Greece’s gross domestic product. In the wake of a struggling economy many of Greece’s coastal villages have turned to tourism to supplement local economies. Preliminary analysis of structural and cultural materials recovered from an excavation on Mitrou, a small islet near the coastal village Tragana located 140 km north of Athens has established the site’s contribution to a fuller understanding of settlement practices in Central Greece from the end of the Bronze Age through the Early Iron Age. The site’s historic importance combined with its scenic coastal setting has considerable potential to be developed into an important tourist site. The physical geography of the region is the product of the complex interaction of coastal, alluvial, fluvial, and seismic processes. This investigation integrates the archaeological material with a geographical analysis employing a variety of geographical techniques (soil and sediment analysis, past climatic data, environmental surveys, and geospatial modeling) to reconstruct the geomorphological history of the site and to evaluate the area as a potential tourist site.     

Manganese ore deposits in Koira-Noamundi province of Iron Ore Group, north Orissa, India: In the light of geochemical signature

Several small Mn–Fe oxide and Mn-oxide ore bodies associated with Precambrian Iron Ore Group of rocks are located within Koira-Noamundi province of north Orissa, India. These deposits are classified into in situ (stratiform), remobilized (stratabound) and reworked categories based on their field disposition. Volcaniclastic/terrigenous shale in large geographic extension is associated with these ore bodies.The in situ ore bodies are characterised by cryptomelane-, romanechite- and hematite-dominating minerals, low Mn/Fe ratio (1.1) and relatively lower abundance of trace (1500–2500 ppm) constituents. In such type of deposits the stratigraphic conformity of oxides with the tuffaceous shale suggests precipitation of Mn and Fe at a time of decreased volcaniclastic/terrigenous contribution. The minor and trace elements were removed from solution by adsorption rather than by precipitation. Both Mn and Fe oxides when precipitated adsorb trace elements strongly but the partitioning of elements takes place during diagenesis. The inter-elemental relationship reveals that Cu, Co, Ni, Pb and Zn were adsorbed on precipitating hydrous Mn oxides and form manganates. Some of these elements probably get desorbed from Fe oxide because of their inability to substitute for Fe³⁺ in the lattice of its oxide. However, P, V, As and Mo were less partitioned and retained in Fe-oxide phase. Positive correlation between Al₂O₃ and SiO₂, MgO, Na₂O, TiO₂ and some traces like Li, Nb, Sc, Y, Zr, Th and U points to their contribution through volcaniclastic/terrigenous detritus of both mafic and acidic composition.The remobilized ore bodies are developed in a later stage through dissolution, remobilization and reprecipitation of Mn oxides in favorable structural weak planes under supergene environment. Increase in average Mn/Fe ratio (8) and trace content (5000–8500 ppm) by 5–2.5 orders of magnitude, respectively, or more above its abundance in adjoining/underlying protore is characteristic of these deposits. The newly formed Mn ores constituting lithiophorite, cryptomelane/romanechite and goethite get quantitatively enriched in traces like Cu, Co, Ni, Pb and Zn. Positive correlation between Mn, Li, Co and Zn is due to the formation of mineral of lithiophorite–chalcophanite group during redistribution and reconcentration of Mn oxide. P and V, which were present in Fe oxide, also get dissolved and reprecipitate with Fe oxyhydroxide in these ores. Some other elements like Y, Th and U show positive relation with Fe. This is probably due to leaching of these elements during chemical weathering of associated shale and getting re-adsorbed in Fe-oxyhydroxide phase.However, under oxidizing environment selective cations like Ba, K, etc. resorb from Mn-structure, resulting in the development of pyrolusite (Mn/Fe>20). In such transformation, trace metals from pyrolusitic structure expels out, resulting thereby in a considerable reduction in total trace value (<3000 ppm).The reworked ore bodies are allochthonous in nature and developed through a number of stages during terrain evolution and lateritisation. Secondary processes such as reworking of pre-existing crust; solution and remobilization; precipitation and cementation and transport, etc. are responsible for their development. Such deposits are usually very low in Mn/Fe ratio (3) and trace content (<2000 ppm).     

清镇式铁矿矿石特征及加工技术性能探讨 ——以猫场铝土矿红花寨、白浪坝矿段铁矿床为例

贵州中部清镇、修文等地石炭系铝土矿底部的铁矿俗称为"清镇式铁矿",与黔中铝土矿共同赋存于下石炭统九架炉组之中。本文在实际勘探工作及通过勘探阶段在钻孔副样中采集的铁矿进行可选性试验基础上,以同类型的清镇市猫场铝土矿红花寨、白浪坝矿段铝土矿共生的铁矿为研究对象,指出该类型铁矿矿石自然类型为赤铁矿和褐铁矿;工业类型为需选铁矿石;矿石矿物主要为赤铁矿,部分赤铁矿水化为针柱状褐铁矿;脉石矿物则以白云石和方解石为主。矿石中可供利用的主要元素是铁,造渣组分主要是硅、铝,其次为钙、镁等。试验结果表明,该矿采用一粗一精一扫的强磁选试验可获得铁精矿TFe含量55. 58%,回收率80. 11%的良好指标,精矿中各元素含量达到H55-Ⅰ类赤铁精矿质量要求,在当前市场条件下采用推荐工艺处理该矿可获利。结论对黔中铝土矿资源的综合勘查开发具有借鉴意义。     

Heating duration of igneous rim formation on a chondrule in the Northwest Africa 3118 CV3oxA carbonaceous chondrite inferred from micro-scale migration of the oxygen isotopes

Due to their common occurrence in various types of chondrites, igneous rims formed on pre-existing chondrules throughout chondrule-forming regions of the solar nebula. Although the peak temperatures are thought to reach similar values to those achieved during chondrule formation events, the heating duration in chondrule rim formation has not been well defined. We determined the two-dimensional chemical and oxygen isotopic distributions in an igneous rim of a chondrule within the Northwest Africa 3118 CV3_oxA chondrite with sub-micrometer resolution using secondary ion mass spectrometry and scanning electron microscopy. The igneous rim experienced aqueous alteration on the CV parent body. The aqueous alteration resulted in precipitation of the secondary FeO-rich olivine (Fa_40–49) and slightly disturbed the Fe-Mg distribution in the MgO-rich olivine phenocrysts (Fa_11–22) at about a 1 μm scale. However, no oxygen isotopic disturbances were observed at a scale greater than 100 nm. The MgO-rich olivine, a primary phase of igneous rim formation, has δ¹⁷O = −6 ± 3‰ and δ¹⁸O = −1 ± 4‰, and some grains contain extreme ¹⁶O-rich areas (δ¹⁷O, δ¹⁸O = ∼−30‰) nearly 10 μm across. We detected oxygen isotopic migration of approximately 1 μm at the boundaries of the extreme ¹⁶O-rich areas. Using oxygen self-diffusivity in olivine, the heating time of the igneous rim formation could have continued from several hours to several days at near liquidus temperatures (∼2000 K) in the solar nebula suggesting that the rim formed by a similar flash heating event that formed the chondrules.     

Phosphate removal from water by naturally occurring shale,sandstone, and laterite: The role of iron oxides and of soluble species

Aqueous phosphate removal by three geomaterials from Ivory Coast was evaluated to determine their potential application as low-cost phosphate adsorbents in wastewater treatment. Batch experiments showed that phosphate uptake strongly depended on pH. Laterite and sandstone dissolution was less pronounced compared to shale. A correlation between concentrations of aqueous cation species released from shale and phosphate uptake was observed. The kinetics were well described using the pseudo-second-order model. Isotherms displayed a saturation level on shale, while phosphate uptake continuously increased for laterite and sandstone. The removal efficiency decreased in the following ranking order: laterite > sandstone > shale. Laterite was also the most efficient adsorbent in column experiments. The high phosphate removal efficiency of laterite (8.3 mg PO₄ g^?1) was attributed to the presence of superparamagnetic low grain sizes of goethite. Laterite is a particularly promising material for further investigation in wastewater treatment technology such as constructed wetlands.     

Geochemistry of Flooded Underground Mine Workings Influenced by Bacterial Sulfate Reduction

Unlike the majority of the water in the flooded mine complex of Butte Montana, which includes the highly acidic Berkeley pit lake, groundwater in the flooded West Camp underground mine workings has a circum-neutral pH and contains at least 8 μM aqueous sulfide. This article examines the geochemistry and stable isotope composition of this unusual H₂S-rich mine water, and also discusses problems related to the colorimetric analysis of sulfide in waters that contain FeS_(aq) cluster compounds. The West Camp mine pool is maintained at a constant elevation by continuous pumping, with discharge water that contains elevated Mn (90 μM), Fe (16 μM), and As (1.3 μM) but otherwise low metal concentrations. Dissolved inorganic carbon in the mine water is in chemical and isotopic equilibrium with rhodochrosite in the mineralized veins. The mine water is under-saturated with mackinawite and amorphous FeS, but is supersaturated with Cu- and Zn-sulfides. However, voltammetry studies show that much of the dissolved sulfide and ferrous iron are present as FeS_(aq) cluster molecules: as a result, the free concentration of the West Camp water is poorly constrained. Concentrations of dissolved sulfide determined by colorimetry were lower than gravimetric assays obtained by AgNO₃ addition, implying that the FeS_(aq) clusters are not completely extracted by the Methylene Blue reagent. In contrast, the clusters are quantitatively extracted as Ag₂S after addition of AgNO₃. Isotopic analysis of co-existing aqueous sulfide and sulfate confirms that the sulfide was produced by sulfate-reducing bacteria (SRB). The H₂S-rich mine water is not confined to the immediate vicinity of the extraction well, but is also present in flooded mine shafts up to 3 km away, and in samples bailed from mine shafts at depths up to 300 m below static water level. This illustrates that SRB are well established throughout the southwestern portion of the extensive (>15 km³) Butte flooded mine complex.     

Organic Matter Diagenesis in Acidic Mine Lakes

The significance of organic matter origin for carbon oxidation via sulfate and iron reduction in the sediments of three acid mine lakes is analyzed. Carbon reactivity was estimated by fitting first‐order expressions to measured rates. Carbon oxidation rates via sulfate and ferric iron reduction ranged from 3.4 to 4.7 mmol m^–2 d^–1 and resembled those reported for freshwater lakes. The estimated reaction constants increased from about 10^–3 a^–1 at the interface to the former mine grounds to 0.05 to 0.2 a^–1 at the current sediment‐water interface. Aquatic organic matter accounted for an estimated 45...75% of total carbon oxidation rates while it amounted only to about 5...14% of the total organic matter that had been deposited. The results of this study suggest that in highly acidic mine lakes the reactivity of the deposited organic matter can rapidly increase after flooding, enhancing carbon oxidation and internal neutralization rates in the sediments.     

A synthesis of iron deposits in the eastern Tianshan,NW China

The northern Xinjiang region is one of the most significant iron metallogenic provinces in China.Iron deposits are found mainly within three regions:the Altay,western Tianshan,and eastern Tianshan orogenic belts.Previous studies have elaborated on the genesis of Fe deposits in the Altay orogenic belt and western Tianshan.However,the geological characteristics and mineralization history of iron deposits in the eastern Tianshan are still poorly understood.In this paper I describe the geological characteristics of iron deposits in the eastern Tianshan,and discuss their genetic types as well as metallogenic-tectonic settings,Iron deposits are preferentially distributed in central and southern parts of the eastern Tianshan.The known iron deposits in the eastern Tianshan show characteristics of magmatic Fe-Ti-V(e.g.,Weiya and Niumaoquan),sedimentary-metamorphic type(e.g.,Tianhu),and iron skarn(e.g.,Hongyuntan).In addition to the abovementioned iron deposits,many iron deposits in the eastern Tianshan are hosted in submarine volcanic rocks with well-developed skarn mineral assemblages.Their geological characteristics and magnetite compositions suggest that they may belong to distal skarns.SIMS zircon U-Pb analyses suggest that the Fe-Ti oxide ores from Niumaoquan and Weiya deposits were formed at 307.7±1.3 Ma and 242.7±1.9 Ma,respectively.Combined with available isotopic age data,the timing of Fe mineralization in the eastern Tianshan can be divided into four broad intervals:Early Ordovician-Early Silurian(476-438 Ma),Carboniferous(335-303 Ma),Early Permian(295-282 Ma),and Triassic(ca.243 Ma).Each of these episodes corresponds to a period of subduction,post-collision,and intraplate tectonics during the Paleozoic and Mesozoic time.