基于互联网的地理信息系统

讨论了基于互联网的地理信息系统的技术构成与解决方案 ,它将成为GIS发展的大势所趋     

无验潮模式下的GPS水下地形测量技术

传统的水下地形测量模式定型于利用GPS测定水底点的平面位置,利用测深仪测定水底点的深度,附之以瞬时潮位资料,获得点位的高程。这种模式在上述条件具备的情况下,可取得完满的结果。但当验潮条件不具备时,该模式将不能获得测点的高程。为了弥补这一缺陷,简化工作流程,提高水下地形测量的精度,本文提出了一种无验潮模式下的水下地形测量思想,该思想不用专门测定潮位,而直接利用GPS的RTK测量技术,辅之以姿态测量和补偿,从而获得高精度的水底点高程。该方法被验证是正确的,希望进一步推广应用。     

地图投影的最小二乘二元多项式拟合的误差估计

探讨了在地图投影的最小二乘二元多项式拟合中参考点的分布对拟合误差的影响,提出了一种基于矩阵的秩亏的方法来判断参考点是否在指定次数的二元多项式空间的代数曲线上,并导出在极小范数最小二乘意义下的拟合多项式的误差估计式,公式表明拟合误差和参考点的最小二乘误差无关。     

MoisturEC: A New R Program for Moisture Content Estimation from Electrical Conductivity Data

Noninvasive geophysical estimation of soil moisture has potential to improve understanding of flow in the unsaturated zone for problems involving agricultural management, aquifer recharge, and optimization of landfill design and operations. In principle, several geophysical techniques (e.g., electrical resistivity, electromagnetic induction, and nuclear magnetic resonance) offer insight into soil moisture, but data‐analysis tools are needed to “translate” geophysical results into estimates of soil moisture, consistent with (1) the uncertainty of this translation and (2) direct measurements of moisture. Although geostatistical frameworks exist for this purpose, straightforward and user‐friendly tools are required to fully capitalize on the potential of geophysical information for soil‐moisture estimation. Here, we present MoisturEC, a simple R program with a graphical user interface to convert measurements or images of electrical conductivity (EC) to soil moisture. Input includes EC values, point moisture estimates, and definition of either Archie parameters (based on experimental or literature values) or empirical data of moisture vs. EC. The program produces two‐ and three‐dimensional images of moisture based on available EC and direct measurements of moisture, interpolating between measurement locations using a Tikhonov regularization approach.     

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Application of Hilbert‐like transforms for enhanced processing of full tensor magnetic gradient data

Commonly, geomagnetic prospection is performed via scalar magnetometers that measure values of the total magnetic intensity. Recent developments of superconducting quantum interference devices have led to their integration in full tensor magnetic gradiometry systems consisting of planar‐type first‐order gradiometers and magnetometers fabricated in thin‐film technology. With these systems measuring directly the magnetic gradient tensor and field vector, a significantly higher magnetic and spatial resolution of the magnetic maps is yield than those produced via conventional magnetometers. In order to preserve the high data quality in this work, we develop a workflow containing all the necessary steps for generating the gradient tensor and field vector quantities from the raw measurement data up to their integration into high­resolution, low­noise, and artefactless two‐dimensional maps of the magnetic field vector. The gradient tensor components are processed by superposition of the balanced gradiometer signals and rotation into an Earth‐centred Earth‐fixed coordinate frame. As the magnetometers have sensitivity lower than that of gradiometers and the total magnetic intensity is not directly recorded, we employ Hilbert‐like transforms, e.g., integration of the gradient tensor components or the conversion of the total magnetic intensity derived by calibrated magnetometer readings to obtain these values. This can lead to a better interpretation of the measured magnetic anomalies of the Earth's magnetic field that is possible from scalar total magnetic intensity measurements. Our conclusions are drawn from the application of these algorithms on a survey acquired in South Africa containing full tensor magnetic gradiometry data.     

Controlling factors of the δ 11B-pH proxy and its research direction

Significant boron isotope fractionation occurs in nature (?70 ‰ to +75 ‰) due to the high geochemical reactivity of boron and the large relative mass difference between ¹⁰B and ¹¹B. Since the 1990s, reconstruction of ancient seawater pH using the isotopic composition of boron in bio-carbonates (δ ¹¹B_carb), and then calculation of the past pCO₂ have become important issues for the international isotope geochemistry community, and are called the δ ¹¹B-pH proxy. Although many achievements have been made by this proxy, various aspects of boron systematics require rigorous evaluation. Based on the previous researches, mechanism of boron isotope fractionation, variation of boron isotope (δ ¹¹B) in nature (especially in bio-carbonates) and controlling factors of the δ ¹¹B-pH proxy, such as the dissociation constant of B(OH)₃ in seawater (pK_a), the δ ¹¹B of seawater (δ ¹¹B_SW), the boron isotopic fractionation factor between B(OH) ₄ ^? and B(OH)₃ (α _4–3), and the incorporated species of boron into bio-carbonates, are reviewed in detail and the research directions of this proxy are proposed. Generally, the controversy about pK_a, δ ¹¹B_sw, and α _4–3 is relatively less, but whether boron incorporated into bio-carbonates only in the form of B(OH) ₄ ^? remains doubtful. In the future, it is required that the physicochemical processes that control boron incorporation into carbonates be rigorously characterized and that the related chemical and isotopic fractionation be quantified. It is also necessary and important to establish a “best-fit empirically equation” between δ ¹¹B_carb and pH of seawater based on the precipitation experiments of inorganic or culture experiments of corals or foraminifera. In addition, extended application of the δ ¹¹B-pH proxy to the earlier part of the Phanerozoic relying on the Brachiopods is worthy of studying. Like other geochemical indicators, there are limiting factors of δ ¹¹B; however, it remains a very powerful tool in the reconstruction of past seawater pH at present.     

论煤层的加积方式

煤层成因是煤地质学的核心。煤层是一种沉积地层,它遵循沉积学、地层学、岩石学以及矿床学的基本规律,也有其特殊性,其成因并不同于煤的成因。传统煤地质学的核心观点是煤层由泥炭沼泽演化而成,其本质就是成煤物质的垂向加积。通过对煤层垂向和侧向加积的分析对比以及大面积稳定展布的厚煤层低自然伽马多峰现象、层理与条带结构等沉积特征的研究,认为成煤物质是机械沉积的,煤层像大多数沉积岩层一样是侧向加积形成的。对于厚煤层而言,多期侧向加积产生了次生垂向加积,其形成过程不是一个简单的、连续的、线性的垂向累加过程,而是一个复杂的、不连续的、非线性的侧向叠合过程,成煤物质是不连续的、多期多源的,厚煤层中普遍存在的夹矸便是其不连续的证据,同时厚煤层是穿时的。煤层侧向加积与较深水或海相沉积共生,是一个有机连续的整体,符合瓦尔特相律和古生态学原理,符合煤层厚度、形态多变及下伏地层沉积体系多种多样,也符合成煤物质超巨量工业富集、含煤地层灰色灰黑色、煤矿床质量优良的事实。     

Hydrologic response of engineered media in living roofs and bioretention to large rainfalls: experiments and modeling

The hydrologic response of engineered media plays an important role in determining a stormwater control measure's ability to reduce runoff volume, flow rate, timing, and pollutant loads. Five engineered media, typical of living roof and bioretention stormwater control measures, were investigated in laboratory column experiments for their hydrologic responses to steady, large inflow rates. The inflow, medium water content response, and outflow were all measured. The water flow mechanism (uniform flow vs. preferential flow) was investigated by analyzing medium water content response in terms of timing, magnitude, and sequence with depth. Modeling the hydrologic process was conducted in the HYDRUS‐1D software, applying the Richards equation for uniform flow modeling, and a mobile–immobile model for preferential flow modeling. Uniform flow existed in most cases, including all initially dry living roof media with bimodal pore size distributions and one bioretention medium with unimodal pore size distribution. The Richards equation can predict the outflow hydrograph reasonably well for uniform flow conditions when medium hydraulic properties are adequately represented by appropriate functions. Preferential flow was found in two media with bimodal pore size distributions. The occurrence of preferential flow is more likely due to the interaction between the bimodal pore structure and the initial water content rather than the large inflow rate.     

富含古罗糖醛酸的褐藻多糖生产菌株的构建

为获得古罗糖醛酸(Guluronate)含量高的细菌胞外褐藻多糖,利用PCR从海洋细菌Pseudomonassp.QDA中克隆了其甘露糖醛酸C-5差向异构酶基因(algG),连接入质粒pMF 54Km,构建了重组表达载体pMF54 Km-algG。利用三亲接合法将pMF54 Km-algG转入菌株QDA中,获得algG过量表达重组菌株QDA-G1。H-NMR测定结果表明,QDA-G所产的褐藻多糖中β-D-甘露糖醛酸(M)与它的C-5差向异构体α-L-古罗糖醛酸(G)的比值为0.38,G的质量分数达到74.2%,比野生菌株QDA提高了26.4%。且重组菌株遗传稳定性良好,连续传代20代后,M/G的比值无明显变化。