Effects of changes in canopy interception on stream runoff response and recovery following clear-cutting of a Japanese coniferous forest in Fukuroyamasawa Experimental Watershed in Japan

Understanding changes in evapotranspiration during forest regrowth is essential to predict changes of stream runoff and recovery after forest cutting. Canopy interception (Ic) is an important component of evapotranspiration, however Ic changes and the impact on stream runoff during regrowth after cutting remains unclear due to limited observations. The objective of this study was to examine the effects of Ic changes on long-term stream runoff in a regrowth Japanese cedar and Japanese cypress forest following clear-cutting. This study was conducted in two 1-ha paired headwater catchments at Fukuroyamasawa Experimental Watershed in Japan. The catchments were 100% covered by Japanese coniferous plantation forest, one of which was 100% clear-cut in 1999 when the forest was 70 years old. In the treated catchment, annual runoff increased by 301 mm/year (14% of precipitation) the year following clear-cutting, and remained 185 mm/year (7.9% of precipitation) higher in the young regrowth forest for 12–14 years compared to the estimated runoff assuming no clear-cutting. The Ic change was −358 mm/year (17% of precipitation) after cutting and was −168 mm/year (6.7% of precipitation) in the 12–14 years old regrowth forest compared to the observed Ic during the pre-cutting period. Stream runoff increased in all seasons, and the Ic change was the main fraction of evapotranspiration change in all seasons throughout the observation period. These results suggest that the change in Ic accounted for most of the runoff response following forest cutting and the subsequent runoff recovery in this coniferous forest.     

Magnetic Reconnection, Turbulence, and Collisionless Shock

A short summary of recent progress in measuring and understanding turbulence during magnetic reconnection in laboratory plasmas is given. Magnetic reconnection is considered as a primary process to dissipate magnetic energy in laboratory and astrophysical plasmas. A central question concerns why the observed reconnection rates are much faster than predictions made by classical theories, such as the Sweet–Parker model based on MHD with classical Spitzer resistivity. Often, the local resistivity is conjectured to be enhanced by turbulence to accelerate reconnection rates either in the context of the Sweet–Parker model or by facilitating setup of the Pestchek model. Measurements at a dedicated laboratory experiment, called MRX or Magnetic Reconnection Experiment, have indicated existence of strong electromagnetic turbulence in current sheets undergoing fast reconnection. The origin of the turbulence has been identified as right-hand polarized whistler waves, propagating obliquely to the reconnecting field, with a phase velocity comparable to the relative drift velocity. These waves are consistent with an obliquely propagating electromagnetic lower-hybrid drift instability driven by drift speeds large compared to the Alfven speed in high-beta plasmas. Interestingly, this instability may explain electromagnetic turbulence also observed in collisionless shocks, which are common in energetic astrophysical phenomena.     

滇西动态重力网的分形特征及空间分辨力

介绍了用分形学描述地球物理观测网非均匀分布和联合应用分形特征与Ｓｈａｎｎｏｎ定理确定最佳网格距的方法。研究了滇西动态重力网的分形特征，它的分形维Ｄｆ＝１．２７，最佳网格距ｒ０＝２８ｋｍ。讨论了１９８６年至１９９４年间网区发生的８次Ｍｓ＞５．０级地震前重力场变化的可信性，指出这些变化的波长均大于１００ｋｍ，至少２倍于网的最小空间分辨力，因而是可信的     

基于STC单片机的实验开发平台的设计

介绍了基于STC89C516RD＋单片机的实验开发平台的硬件电路设计、ISP编程、软件开发实例及系统的抗干扰措施.为帮助学生学习单片机技术,同时也为有经验者开发和调试产品打下基础.     

Asymmetrically zoned reaction rims: assessment of grain boundary diffusivities and growth rates related to natural diffusion-controlled mineral reactions

This study explores garnet coronas around hedenbergite, which were formed by the reaction plagioclase + hedenbergite→garnet + quartz, to derive information about diffusion paths that allowed for material redistribution during reaction progress. Whereas quartz forms disconnected single grains along the garnet/hedenbergite boundaries, garnet forms ～20‐μm‐wide continuous polycrystalline rims along former plagioclase/hedenbergite phase boundaries. Individual garnet crystals are separated by low‐angle grain boundaries, which commonly form a direct link between the reaction interfaces of the plagioclase|garnet|hedenbergite succession. Compositional variations in garnet involve: (i) an overall asymmetric compositional zoning in Ca, Fe²⁺, Fe³⁺ and Al across the garnet layer; and (ii) micron‐scale compositional variations in the near‐grain boundary regions and along plagioclase/garnet phase boundaries. These compositional variations formed during garnet rim growth. Thereby, transfer of the chemical components occurred by a combination of fast‐path diffusion along grain boundaries within the garnet rim, slow diffusion through the interior of the garnet grains, and by fast diffusion along the garnet/plagioclase and the garnet/hedenbergite phase boundaries. Numerical simulation indicates that diffusion of Ca, Al and Fe²⁺ occurred about three to four, four and six to seven orders of magnitude faster along the grain boundaries than through the interior of the garnet grains. Fast‐path diffusion along grain boundaries contributed substantially to the bulk material transfer across the growing garnet rim. Despite the contribution of fast‐path diffusion, bulk diffusion through the garnet rim was too slow to allow for chemical equilibration of the phases involved in garnet rim formation even on a micrometre scale. Based on published garnet volume diffusion data the growth interval of a 20‐μm‐wide garnet rim is estimated at ～10³–10⁴ years at the inferred reaction conditions of 760 ± 50 °C at 7.6 kbar. Using the same parameterization of the growth law, 100‐μm‐ and 1‐mm‐thick garnet rims would grow within 10⁵–10⁶ and 10⁶–10⁷ years respectively.     

Experimental constraints on the effects of pressure and H2O on the fractional crystallization of high-Mg island arc basalt

H₂O-undersaturated melting experiments of synthesized basalt (SiO₂ = 50.7 wt.%, MgO = 8.3 wt.%, Mg# = 60) were conducted at fO₂ corresponding to NNO+1 and NNO−1 to clarify the effects of pressure (2–7 kbar) and H₂O on fractional crystallization in island arcs. H₂O content was ranged from nominally anhydrous to 4.4 wt.%. Differentiation trends, namely the liquid lines of descent, change sensitively according to pressure-H₂O relations. Tholeiitic differentiation trends are reproduced with H₂O ≤ ∼2 wt.% in primary magma. With such quantities of H₂O, fractional crystallization is controlled by olivine + plagioclase at 2 kbar. Increasing the pressure from 2 to ≥4 kbar induces early crystallization of orthopyroxene instead of olivine and therefore SiO₂ enrichment in the residual melts is suppressed. Increasing H₂O (≥ ∼2 wt.% in primary magma) stabilizes clinopyroxene relative to orthopyroxene and/or magnetite. Although the phase relations and proportions strongly depend on fO₂ and H₂O content, differentiation trends are always calc-alkaline.     

An experimental study of the grain-scale processes of peridotite melting: implications for major and trace element distribution during equilibrium and disequilibrium melting

The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar P–T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Si diffusion in zircon

Self-diffusion of Si under anhydrous conditions at 1 atm has been measured in natural zircon. The source of diffusant for experiments was a mixture of ZrO₂ and ³⁰Si-enriched SiO₂ in 1:1 molar proportions; experiments were run in crimped Pt capsules in 1-atm furnaces. ³⁰Si profiles were measured with both Rutherford backscattering spectrometry (RBS) and nuclear reaction analysis with the resonant nuclear reaction ³⁰Si(p,γ)³¹P. For Si diffusion normal to c over the temperature range 1,350–1,550°C, we obtain an Arrhenius relation D = 5.8 exp(−702 ± 54 kJ mol⁻¹/RT) m² s⁻¹ for the NRA measurements, which agrees within uncertainty with an Arrhenius relation determined from the RBS measurements [62 exp(−738 ± 61 kJ mol⁻¹/RT) m² s⁻¹]. Diffusion of Si parallel to c appears slightly faster, but agrees within experimental uncertainty at most temperatures with diffusivities for Si normal to c. Diffusion of Si in zircon is similar to that of Ti, but about an order of magnitude faster than diffusion of Hf and two orders of magnitude faster than diffusion of U and Th. Si diffusion is, however, many orders of magnitude slower than oxygen diffusion under both dry and hydrothermal conditions, with the difference increasing with decreasing temperature because of the larger activation energy for Si diffusion. If we consider Hf as a proxy for Zr, given its similar charge and size, we can rank the diffusivities of the major constituents in zircon as follows: D _Zr < D _Si << D _{O, dry} < D _{O, ‘wet’}.     

钱二块铀矿床采铀注液结垢趋势的理论分析与预测

用离子系数矩阵法对钱二块铀矿床地浸采铀试验注液中存在的独立离子反应进行了确定,由溶度积规则及反应平衡原理,借助Matlab编程,估算出了钱二块铀矿床地浸采铀试验注液可能会生成的沉淀物种类及数量,为防治结垢提供了一定的理论依据.     

海浪的条件特征周期

在海浪波面高度为正态分布的假定下,导出一种以给定波高为条件的条件周期概率密度函数.与风浪槽中测量数据比较,结果表明,在窄谱情况下此概率密度函数与实验室风浪的实际符合良好.根据此密度函数定义了3种条件特征周期,并导出它们与平均周期的关系式.根据这些关系对有关海洋工程上的一些问题作了解释和讨论.