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首页> 外文期刊>Journal of Geochemical Exploration: Journal of the Association of Exploration Geochemists >The regional geochemical baseline soil survey of southern New Zealand: Design and initial interpretation
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The regional geochemical baseline soil survey of southern New Zealand: Design and initial interpretation

机译:新西兰南部的区域地球化学基线土壤调查:设计和初步解释

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A multivariate geochemical baseline survey of soils from southern New Zealand has been completed. Soil samples were collected from 0 to 30 cm 'A-depth' and 50-70 cm 'B-depth' at 348 sites on an 8 km-spaced grid covering 40,000 km(2) of the Southland and southern Otago regions. The sub-180 mu m fraction of all samples was analysed by inductively coupled plasma mass spectrometry following aqua regia (partial) digestion for 65 elements, and by Leco CS320 element analyser for total C and S. Sub-sets of the samples were analysed by XRF for 12 oxides/elements. Significant chemical variation in the soil samples can be linked to variations in source geology, soil type, climate and topography. Relatively high concentrations of certain elements (e.g. S, P, Pb, Hg, Cd), particularly in the A-depth, are attributed to anthropogenic sources such as fertilisers, paints, vehicle emissions or industrial emissions. Other elevated element concentrations, especially those in B-depth samples, are probably natural with high As, Bi, Sb and W reflecting proximity to Au mineralisation, Pt and Re near PGE mineralisation, and accumulation of heavy mineral-associated elements such as Cr in alluvium-derived soils related to the effects of both source material and hydraulic effects on flood plains. This study provides an important baseline that will benefit government, environmental, agricultural, forestry and mining sectors through improved regulatory guidelines and understanding of the regional geochemical landscape. This survey design, with minimal modification, is suitable for a national geochemical baseline survey for New Zealand. (C) 2016 Elsevier B.V. All rights reserved.
机译:新西兰南部土壤的多变量地球化学基线调查已经完成。在一个间隔为8 km的网格上的348个站点上,从0到30 cm的“ A深度”和50-70 cm的“ B深度”收集了土壤样本,覆盖了40,000 km(2)的南国和奥塔哥南部地区。水(部分)消化后,通过电感耦合等离子体质谱法分析所有样品中小于180微米的部分,其中65个元素,然后通过Leco CS320元素分析仪分析总C和S。 XRF用于12种氧化物/元素。土壤样品中明显的化学变化可能与源地地质,土壤类型,气候和地形的变化有关。某些元素(例如S,P,Pb,Hg,Cd)的相对较高浓度(尤其是在A深度)归因于人为来源,例如肥料,油漆,车辆排放物或工业排放物。其他升高的元素浓度(尤其是在B深度样品中)也很自然,其中As,Bi,Sb和W含量较高,反映出接近Au矿化,Pt和Re接近PGE矿化,以及重金属相关元素(如Cr)的积累。冲积土与源物质和水力作用对洪泛平原的影响有关。这项研究提供了重要的基线,通过改进的监管指南和对区域地球化学景观的了解,将使政府,环境,农业,林业和采矿业受益。这种勘测设计经过最少的修改,适用于新西兰的国家地球化学基线勘测。 (C)2016 Elsevier B.V.保留所有权利。

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