基于非线性平差模型的坐标转换公式

用线性近似法以及非线性参数估计法讨论了直角坐标系七参数转换模型，指出改进的Gauss-Newton方法具有理论严密、计算简洁、易于编程、精度较高等持点。对于处理类似坐标转换的非线性模型具有重要的理论和实践意义。     

无地面控制GPS辅助光束法区域网平差

介绍了在WGS-84坐标系中进行GPS辅助光束法区域网平差的基本原理以及利用大地水准面拟合方法实施大地高与正常高的变换方法。利用新疆库尔勒地区1：25000和1：50000实际航摄资料验证了理论与程序实现的正确性。试验结果表明，无地面控制GPS辅助光束法区域网平差可用于中小比例尺测图的加密，在WGS-84坐标系中可以获得较高的点定位精度，而在国家80坐标系下，利用大地水；隹面拟合前后的GPS摄站坐标进行GPS辅助光束法区域网平差，加密精度没有明显差异。     

Channel geometry of mountain streams in New Zealand

A dataset of 21 study reaches in the Porter and Kowai rivers (eastern side of the South Island), and 13 study reaches in Camp Creek and adjacent catchments (western side of the South Island) was used to examine downstream hydraulic geometry of mountain streams in New Zealand. Streams in the eastern and western regions both exhibit well-developed downstream hydraulic geometry, as indicated by strong correlations between channel top width, bankfull depth, mean velocity, and bankfull discharge. Exponents for the hydraulic geometry relations are similar to average values for rivers worldwide. Factors such as colluvial sediment input to the channels, colluvial processes along the channels, tectonic uplift, and discontinuous bedrock exposure along the channels might be expected to complicate adjustment of channel geometry to downstream increases in discharge. The presence of well-developed downstream hydraulic geometry relations despite these complicating factors is interpreted to indicate that the ratio of hydraulic driving forces to substrate resisting forces is sufficiently large to permit channel adjustment to relatively frequent discharges.     

Direct Current Plasma Emission Spectrometric Determination of Major, Minor and Trace Elements in Microwave Oven Acid Leachates of Powdered Whole Coal Samples

Major concentrations of Al₂O₃, Fe₂O₃, MgO, CaO, Na₂O and K₂O, minor levels of TiO₂, P₂O₅ and thirty petrologically, geochemically and environmentally significant trace elements have been determined in microwave oven acid leachates of whole powdered coal samples by direct current plasma‐atomic emission spectrometry (DCP‐AES). A single sample preparation procedure was suitable for all the determinations with no additional dilution step for major elements solution. Dried samples (0.5 g) were treated in low‐pressure PFA digestion vessels with HF/HCl/HNO₃/HClO₄ acids to quantitatively extract the analytes from the bulk material, while leaving the major part of organic matrix as a residue. The major constituents of geological samples, in particular the easily ionised elements (EIEs) such as alkali and alkaline earths, may complicate the instrumental determinations in DCP‐AES because of differential enhancements of elemental emission intensities and stray light interferences. Taking account of these factors, the coal matrix is considered to have very low major oxide totals as compared to many other common geo‐environmental and related materials (rocks, sediments, soil, ashes etc.). The sample size employed here, while yielding a relatively concentrated solution to cover a wide range of elemental determinations, provided a sample matrix that significantly diminished interferences for DCP measurements. The need for closely matching the unknowns and calibrators was eliminated except for overall acidity and an excess quantity of caesium for EIE buffering. Calibration of the spectrometer was accomplished by simple aqueous single element solutions as high concentration calibrators in addition to a reagent blank as a low concentration calibrator. Two point working curves were established to allow for the maximum concentrations of each element expected in the unknowns. The precision of determinations under routine conditions as well as the reproducibility of the leaching and precision of instrumental measurements have been evaluated. Relative standard deviations (RSD) were of 1–2% for those elements whose concentrations in solid samples were well above the limits of quantification. Method detection limits in the buffered solutions were also evaluated. To evaluate the accuracy of the microwave oven‐DCP method a suite of eight certified coal reference materials of differing rank, were analysed with good agreement with the certified and/or available published data. Results are presented for the uncertified major oxides in the AR series reference materials.     

云南沿边境地带生态环境3S监测、 评价与调控研究

本文利用全球新千年整体生态系统评估的理论，以云南省沿边境地带生态系统变化跨境生态安全为研究对象，探寻并揭示我国陆疆系统的跨境生态系统变化监测、评价和生态安全综合调控的基础理论与信息机理；进而研究基于“3S”云南沿边境地带的生态环境监测、评价与综合调控的方法和关键技术，包括方法和技术体系的建立、指标体系的建立、多尺度效应和尺度转换、数学模型的建立、综合调控模式和决策方案的建立等；在案例研究部分，建立了背景数据库，然后选择大、中、小尺度进行了全区生态环境现状评价，重点河道、典型路段和重点口岸的影响评价和预测预报研究，最后进行了综合调控模式和方案的探讨，并对研究结果进行了动态仿真和虚拟表达研究。     

基于可持续发展的广东省城市供水价格改革探讨

针对目前城市供水价格计算与计量方式不合理和突出的水资源供需矛盾,提出了按全成本水价模式测算广东省城市供水价格,并采用阶梯水价、两部制水价和季节水价计量方式逐步达到全成本水价的措施与实施步骤,确保水资源的持续利用支撑广东省经济社会的可持续发展.     

Late Quaternary sea‐level change and evolution of Belfast Lough,Northern Ireland: new offshore evidence and implications for sea‐level reconstruction

The interplay of eustatic and isostatic factors causes complex relative sea‐level (RSL) histories, particularly in paraglacial settings. In this context the past record of RSL is important in understanding ice‐sheet history, earth rheology and resulting glacio‐isostatic adjustment. Field data to develop sea‐level reconstructions are often limited to shallow depths and uncertainty exists as to the veracity of modelled sea‐level curves. We use seismic stratigraphy, 39 vibrocores and 26 radiocarbon dates to investigate the deglacial history of Belfast Lough, Northern Ireland, and reconstruct past RSL. A typical sequence of till, glacimarine and Holocene sediments is preserved. Two sea‐level lowstands (both max. ?40 m) are recorded at c. 13.5 and 11.5k cal a bp . Each is followed by a rapid transgression and subsequent periods of RSL stability. The first transgression coincides temporally with a late stage of Meltwater Pulse 1a and the RSL stability occurred between c. 13.0 and c. 12.2k cal a bp (Younger Dryas). The second still/slowstand occurred between c. 10.3 and c. 11.5k cal a bp . Our data provide constraints on the direction and timing of RSL change during deglaciation. Application of the Depth of Closure concept adds an error term to sea‐level reconstructions based on seismic stratigraphic reconstructions.     

Daily salinity fluctuation alleviates salt stress on seedlings of the mangrove Bruguiera gymnorhiza

Salinity is a vital factor that regulates leaf photosynthesis and growth of mangroves, and it frequently undergoes large seasonal and daily fluctuations creating a range of environments – oligohaline to hyperhaline. Here, we examined the hypotheses that mangroves benefit opportunistically from low salinity resulting from daily fluctuations and as such, mangroves under daily fluctuating salinity (FS) grow better than those under constant salinity (CS) conditions. We compared growth, salt accumulation, gas exchange, and chlorophyll fluorescence of leaves of mangrove Bruguiera gymnorhiza seedlings growing in freshwater (FW), CS (15 practical salinity units, PSU), and daily FS (0–30 PSU, average of 4.8 PSU) conditions. The traits of FS-treated leaves were measured in seedlings under 15 PSU. FS-treated seedlings had greater leaf biomass than those in other treatment groups. Moreover, leaf photosynthetic rate, capacity to regulate photoelectron uptake/transfer, and leaf succulence were significantly higher in FS than in CS treatment. However, leaf water-use efficiency showed the opposite trend. In addition to higher concentrations of Na⁺ and Cl⁻, FS-treated leaves accumulated more Ca²⁺ and K⁺. We concluded that daily FS can enhance water absorption, photosynthesis, and growth of leaves, as well as alter plant biomass allocation patterns, thereby positively affecting B. gymnorhiza. Mangroves that experience daily FS may increase their adaptability by reducing salt build-up and water deficits when their roots are temporally subjected to low salinity or FW and by absorbing sufficient amounts of Na⁺ and Cl⁻ for osmotic adjustment when their roots are subsequently exposed to saline water.