福建李家坊金矿床磁铁矿成因及其对金矿化过程的指示

福建泰宁李家坊金矿床位于武夷山成矿带中段,为闽西北何宝山矿田内新发现的一个中型金矿床,成因类型尚未明确。磁铁矿是该矿床中常见的氧化物,文章应用磁铁矿微量元素特征对李家坊金矿床成矿过程与成因类型进行约束。基于野外地质踏勘和钻孔岩芯编录,结合室内详细的岩相学观察,依据磁铁矿的结构和矿物共生组合,文章将其分为4种类型（Mt1a、Mt1b、Mt2和Mt3）。其中,Mt1a位于铜金矿脉边缘,呈板柱状,与绿泥石共生; Mt1b位于铜金矿脉边缘,呈自形-半自形粒状,与绿泥石-赤铁矿共生; Mt2位于铜金矿脉中,呈脉状产出,穿插早阶段的石英-黄铁矿脉,与绿泥石-绿帘石共生; Mt3位于铜金矿脉中,呈半自形-他形粒状,与绿帘石-赤铁矿共生,被后阶段黄铜矿包裹、交代。金主要以自然金和银金矿的形式赋存于Mt3中。原位微区分析结果表明,李家坊金矿不同类型磁铁矿均属于热液型磁铁矿。此外,从Mt1a型到Mt3型磁铁矿,w（Ti）呈逐渐降低的趋势,指示热液流体逐渐向低温条件演化; w（V）表现出先降低后升高再降低的变化规律,暗示热液流体的氧逸度有明显波动,但总体呈升高趋势。磁铁矿的显微结构和化学组成具矽卡岩型矿化特征,是判断矿床成因类型的证据。其中,Mt3型磁铁矿与Au矿化密切相关,其矿物组合与微量元素特征可指示金在低温高氧逸度的环境下沉淀。     

河南漯河市明化镇组温热水地球化学特征及成因

全球环境污染形势依然严峻,加大地热等可再生能源开发力度已成为人类社会的共识。在系统梳理河南漯河地热地质条件基础上,以新近系明化镇组温热水为主要研究对象,通过采样化验,结合所收集资料,对其水化学场、温度场、同位素等进行研究,提出了漯河地热地质成因模式。研究结果表明:河南漯河温热水水化学类型较为复杂,以Cl-Na型、Cl-Na·Ca型、Cl·SO₄-Na型为主,次为Cl·HCO₃-Na型和SO₄·Cl-Na型。漯河新近系明化镇组地热水以沉积水为主,有少量的侧向补给,补给源主要为来自西部及西北部山丘区的大气降水,循环深度为1 320 m,属于典型的传导型地热系统。     

新疆苇湖梁煤矿塌陷区遥感监测研究

苇湖梁煤矿已有50多年的开采历史, 长期的地下开采造成了严重的地面塌陷。本文将新疆苇湖梁煤矿塌陷区作为研究区, 以2013年的IKONOS高分遥感影像为主要数据源, 以ArcGIS为支撑平台, 采用人机交互的解译方法对塌陷区的相关信息进行提取, 结合实地调查验证的方法, 分析研究区内地质灾害的特征。通过遥感调查发现: 研究区内发育规模较大、位于塌陷区周围的拉伸区的地裂缝约有64条;塌陷坑(群)约有94个, 主要分布于南北塌陷槽及两侧;塌陷回填区总面积达0.92 km², 并在回填区发现了3个新塌陷坑。本文充分发挥了遥感技术宏观性强、速度快的特点, 调查结果反映了塌陷区灾害的实际情况。     

湖北铜绿山铜铁矿床中煌斑岩的矿物学特征及岩石成因初探

湖北铜绿山矽卡岩型铜铁矿床处于长江中下游铁铜成矿带西部的鄂东南矿集区。最近我们在该矿区工作中采集到两条侵入于含矿石英二长闪长玢岩中的煌斑岩脉。本文对这些煌斑岩脉进行了详细的镜下岩相学观察,并对其中造岩矿物黑云母、辉石和长石进行了电子探针成分分析。根据这些数据本文论述了煌斑岩的物源、形成环境以及岩浆体系的物理化学条件。研究表明,煌斑岩中云母为富镁黑云母,其形成的岩浆体系处于中低氧逸度(近Ni-Ni O);黑云母与全岩都具有高钛特征,表明煌斑岩的物源深度可能来自较深部地幔(如软流圈)。煌斑岩中辉石为单斜辉石,环带较为发育,有韵律环带和正环带,其韵律环带的形成可能是由于岩浆温压环境存在振荡性变化而形成的。铜绿山矿床中煌斑岩属于云煌岩;其岩浆来源具幔源性,受到地壳的混染作用不强。     

江西九瑞矿集区南港成矿远景区煌斑岩中辉石矿物成分特征与岩浆演化过程

九瑞矿集区隶属于长江中下游铜-铁-金成矿带,该矿集区内主要发育有武山、城门山、洋鸡山、丁家山等大中型铜金多金属矿床。区内的南港成矿远景预测区位于横立山-黄桥向斜的南翼,地质条件与该向斜北翼的武山铜矿基本一致。本文以南港地区发现的煌斑岩为研究对象,对其中的辉石进行了详细的岩相学和电子探针成分分析工作,来探讨煌斑岩的演化过程及岩石成因。测试结果显示,南港煌斑岩中的辉石,具有高Ca、高Mg,低Ti,贫Al、贫Fe的特点。斑晶中的辉石属于透辉石和普通辉石,基质中的辉石则属于普通辉石。辉石斑晶的viAl和Na2O含量很低,指示其形成压力较小。由早到晚从斑晶到基质,辉石向着富铁富钙的方向演化。辉石发育有反环带及韵律环带,显示在岩浆房中可能受到过岩浆混合作用的影响。辉石的矿物化学特征指示南港煌斑岩属碱性岩石系列。     

天星河、文峰河流域岩溶水化学及影响因素

重庆东北部地区巫溪天星河、文峰河的岩溶流域水化学特征研究结果表明:研究区泉水样品的p H值为6.47~8.28,平均值为7.79;流域河水饱和指数(SIc)的平均值为0.14,表明其变化受到流域碳酸盐岩分布的控制。水化学类型以HCO3-Ca型水为主,Ca2+和HCO-3平均分别占阳、阴离子的75%和82%。通过分析Gibbs图,发现泉水的主要组分属于"岩石风化类型",主要反映了岩石的溶解作用对泉水水化学的影响。流域内部分水样NO-3和SO2-4较高,可能是受工农业生产等人类活动的影响引起,此外硫酸也参与了碳酸盐矿物的溶解。     

From the Seam to the Stove: greenhouse gas assessment and the coal seam gas industry in Australia

In Australia, Coal Seam Gas (CSG) is a relatively new source of natural gas commonly advocated as a lower greenhouse gas (GHG) emissions alternative to coal. This study investigates how GHG emissions have been, and potentially could be, assessed within the Australian CSG industry. The research involved a document analysis of several Environmental Impact Statements (EISs) and consultant reports prepared as part of the Environmental Impact Assessment (EIA) process for major CSG projects in New South Wales (NSW) and Queensland (Qld). There were found to be inconsistencies in the conduct of greenhouse assessment by the CSG industry, including how complete and transparent assessments were, as well as how effectively they addressed project emission intensity and cumulative impacts. There were also found to be large inconsistencies between assessments carried out for Qld projects and those for NSW projects, likely because of differences in how assessment requirements are applied by planning bodies. This study also highlights how alternative assessment approaches, such as Cumulative Impact Assessment (CIA) and Strategic Environmental Assessment (SEA), have potential to enable a broader and more consistent understanding of emission sources that cross a range of geographical and project boundaries.     

An approach of surface coal fire detection from ASTER and Landsat-8 thermal data: Jharia coal field,India

Radiant temperature images from thermal remote sensing sensors are used to delineate surface coal fires, by deriving a cut-off temperature to separate coal-fire from non-fire pixels. Temperature contrast of coal fire and background elements (rocks and vegetation etc.) controls this cut-off temperature. This contrast varies across the coal field, as it is influenced by variability of associated rock types, proportion of vegetation cover and intensity of coal fires etc. We have delineated coal fires from background, based on separation in data clusters in maximum v/s mean radiant temperature (13th band of ASTER and 10th band of Landsat-8) scatter-plot, derived using randomly distributed homogeneous pixel-blocks (9 × 9 pixels for ASTER and 27 × 27 pixels for Landsat-8), covering the entire coal bearing geological formation. It is seen that, for both the datasets, overall temperature variability of background and fires can be addressed using this regional cut-off. However, the summer time ASTER data could not delineate fire pixels for one specific mine (Bhulanbararee) as opposed to the winter time Landsat-8 data. The contrast of radiant temperature of fire and background terrain elements, specific to this mine, is different from the regional contrast of fire and background, during summer. This is due to the higher solar heating of background rocky outcrops, thus, reducing their temperature contrast with fire. The specific cut-off temperature determined for this mine, to extract this fire, differs from the regional cut-off. This is derived by reducing the pixel-block size of the temperature data. It is seen that, summer-time ASTER image is useful for fire detection but required additional processing to determine a local threshold, along with the regional threshold to capture all the fires. However, the winter Landsat-8 data was better for fire detection with a regional threshold.     

Accuracy and precision of different sampling strategies and flux integration methods for runoff water: comparisons based on measurements of the electrical conductivity

Because of their fast response to hydrological events, small catchments show strong quantitative and qualitative variations in their water runoff. Fluxes of solutes or suspended material can be estimated from water samples only if an appropriate sampling scheme is used. We used continuous in‐stream measurements of the electrical conductivity of the runoff in a small subalpine catchment (64 ha) in central Switzerland and in a very small (0·16 ha) subcatchment. Different sampling and flux integration methods were simulated for weekly water analyses. Fluxes calculated directly from grab samples are strongly biased towards high conductivities observed at low discharges. Several regressions and weighted averages have been proposed to correct for this bias. Their accuracy and precision are better, but none of these integration methods gives a consistently low bias and a low residual error. Different methods of peak sampling were also tested. Like regressions, they produce important residual errors and their bias is variable. This variability (both between methods and between catchments) does not allow one to tell a priori which sampling scheme and integration method would be more accurate. Only discharge‐proportional sampling methods were found to give essentially unbiased flux estimates. Programmed samplers with a fraction collector allow for a proportional pooling and are appropriate for short‐term studies. For long‐term monitoring or experiments, sampling at a frequency proportional to the discharge appears to be the best way to obtain accurate and precise flux estimates. Copyright © 2006 John Wiley & Sons, Ltd.     

Response of surface water chemistry to reduced levels of acid precipitation: comparison of trends in two regions of New York,USA

In light of recent reductions in sulphur (S) and nitrogen (N) emissions mandated by Title IV of the Clean Air Act Amendments of 1990, temporal trends and trend coherence in precipitation (1984–2001 and 1992–2001) and surface water chemistry (1992–2001) were determined in two of the most acid‐sensitive regions of North America, i.e. the Catskill and Adirondack Mountains of New York. Precipitation chemistry data from six sites located near these regions showed decreasing sulphate (SO₄^2?), nitrate (NO₃^?), and base cation (C_B) concentrations and increasing pH during 1984–2001, but few significant trends during 1992–2001. Data from five Catskill streams and 12 Adirondack lakes showed decreasing trends in SO₄^2? concentrations at all sites, and decreasing trends in NO₃^?, C_B, and H⁺ concentrations and increasing trends in dissolved organic carbon at most sites. In contrast, acid‐neutralizing capacity (ANC) increased significantly at only about half the Adirondack lakes and in one of the Catskill streams. Flow correction prior to trend analysis did not change any trend directions and had little effect on SO₄^2? trends, but it caused several significant non‐flow‐corrected trends in NO₃^? and ANC to become non‐significant, suggesting that trend results for flow‐sensitive constituents are affected by flow‐related climate variation. SO₄^2? concentrations showed high temporal coherence in precipitation, surface waters, and in precipitation–surface water comparisons, reflecting a strong link between S emissions, precipitation SO₄^2? concentrations, and the processes that affect S cycling within these regions. NO₃^? and H⁺ concentrations and ANC generally showed weak coherence, especially in surface waters and in precipitation–surface water comparisons, indicating that variation in local‐scale processes driven by factors such as climate are affecting trends in acid–base chemistry in these two regions. Copyright © 2005 John Wiley & Sons, Ltd.