四川省国土资源信息化建设的现状与对策

国土资源信息化是一项长期的战略任务和一个不断发展的过程，信息化建设涉及到现有国土资源管理工作运作机制的调整和业务流的重组。针对四川省国土资源信息化建设，本文在开展全面深入调查四川省信息化建设现状的基础上，探讨了全省在信息化建设中所面临的诸多问题，并相应提出解决对策和建议，为今后我省国土资源管理信息化建设提供了参考。     

Temporal Variability of Iron Speciation in Coastal Rainwater

Iron occurs in rain as particulateand dissolved Fe and includes both Fe(II) and Fe(III)species. Model calculations and correlation analysisindicate Fe(II)(aq) occurs almost exclusively as thefree ion whereas Fe(III)(aq) occurs as both ironoxalate and Fe(OH)₂ ⁺(aq) with largevariations over the pH range from 4.0 to 5.0. Complexation with humic-like compounds may also beimportant for Fe(III)(aq); however, the concentrationand structural characteristics of these compounds haveyet to be determined. 112 rain samples were collectedfor iron analysis in Wilmington, North Carolina,between 1 July 1997, and 30 June 1999. Total iron,particulate iron and Fe(III)(aq) were higher inconcentration in summer and spring rain relative towinter and autumn rain. Fe(II)(aq) concentrations, incontrast, did not vary seasonally. Particulate iron,which was approximately half the total rainwater iron,was highest between noon and 6 p.m. (EST), probably dueto more intense regional convection including land-seabreezes during that time. The ratio ofFe(II)(aq)/Fe(III)(aq) was also highest in rainreceived between noon and 6 p.m., which most likelyreflects photochemical reduction of Fe(III)(aq)complexes to form Fe(II)(aq). A conceptual modeldepicting the interplay between iron species, lightintensity and organic ligands in rainwater ispresented.     

Global two dimensional chemistry model and simulation of atmospheric chemical composition

1.IntroductionAgreatchangehastakenplaceinglobalatmosphericchemicalcompositionbecauseofhumanactivitiessinceindustrialrevolution.Numericalsimulationisaneffectivetooltostudythechangeoftracegases.Inthelasttwentyyears,two--dimensionalchemical/transportmodelshavebeenextensivelydevelopedtosimulatethedistributionsoftracers(GidelandCrutzen,1983;Hough,1991;LawandPyle1993).Inordertopredictthefuturepossiblechangesofatmosphericspecies,itisnecessarytohaveabetterunderstandingofprocessessuchasemission,trans…     

Annual and semiannual variations in the ionospheric F2-layer. I. Modelling

Annual, seasonal and semiannual variations of F2-layer electron density (NmF2) and height (hmF2) have been compared with the coupled thermosphere-ionosphere-plasmasphere computational model (CTIP), for geomagnetically quiet conditions. Compared with results from ionosonde data from midlatitudes, CTIP reproduces quite well many observed features of NmF2, such as the dominant winter maxima at high midlatitudes in longitude sectors near the magnetic poles, the equinox maxima in sectors remote from the magnetic poles and at lower latitudes generally, and the form of the month-to-month variations at latitudes between about 60°N and 50°S. CTIP also reproduces the seasonal behaviour of NmF2 at midnight and the summer-winter changes of hmF2. Some features of the F2-layer, not reproduced by the present version of CTIP, are attributed to processes not included in the modelling. Examples are the increased prevalence of the winter maxima of noon NmF2 at higher solar activity, which may be a consequence of the increase of F2-layer loss rate in summer by vibrationally excited molecular nitrogen, and the semiannual variation in hmF2, which may be due to tidal effects. An unexpected feature of the computed distributions of NmF2 is an east-west hemisphere difference, which seems to be linked to the geomagnetic field configuration. Physical discussion is reserved to the companion paper by Rishbeth et al.     

Controls of dimethyl sulphide in the Bay of Bengal during BOBMEX-Pilot cruise 1998

The air-sea exchange is one of the main mechanisms maintaining the abundances of trace gases in the atmosphere. Some of these, such as carbon dioxide and dimethyl sulphide (DMS), will have a bearing on the atmospheric heat budget. While the former facilitates the trapping of radiation (greenhouse effect) the latter works in the opposite direction through reflectance of radiation back into space by sulphate aerosols that form from oxidation of DMS in atmosphere. Here we report on the first measurements made on DMS in the Bay of Bengal and the factors regulating its abundance in seawater. Phytoplankton alone does not seem to control the extent of DMS concentrations. We find that changes in salinity could effectively regulate the extent of DMSP production by marine phytoplankton. In addition, we provide the first ever evidence to the occurrence of DMS precursor, DMSP, in marine aerosols collected in the boundary layer. This suggests that the marine aerosol transport of DMSP will supplement DMS gaseous evasion in maintaining the atmospheric non-sea salt sulphur budget.     

绿色分析化学技术的研究进展

绿色分析化学技术已成为国际分析化学的前沿,其目标是利用以好的方法和原理,尽量不用或少用有在化学试剂,将环境污染减少到最低限度,目前的研究主要集中于环境友好的样品处理和富集技术,如微波消解、微波萃取、超临界流体萃取、固相萃取、固相微萃取和膜萃取等,以及绿色分析技术,如用开发仪器的功能来消除干扰,从而取代使用掩蔽试剂,将不机相测定变为水相测定等,文章对上述内容进行了综述,引用近期文献５４篇。     

Hornblende geothermometry of amphibolite layers of the Popple Hill gneiss, north-west Adirondack Lowlands, New York, USA

The exchange reaction tschermakite+2 diopside+2 quartz=tremolite+2 anorthite (HPCQ), in combination with the thermodynamic database TWQ (version 1.02, Berman, 1991), has been evaluated for its usefulness as a geothermometer. This reaction, which is both water conserving (independent of water fugacity) and which does not require the presence of garnet, is well suited for studying pyroxene‐bearing amphibolites. As an application of this geothermometer, we have re‐examined the amphibolites occurring in the Popple Hill gneiss of the Adirondack Lowlands of New York, USA, to better understand the magnitude of temperature variation preserved in the amphibolites themselves in this classic locality. At an assumed constant pressure of 7 kbar, the temperatures range from 619 to 682 °C from Edwards to Pierrepont and are uncorrelated with either distance along the strike of the region or with modal mineralogical variations. Hornblende exhibits a narrow compositional range suggesting that there has been little or no thermal gradient along the strike of the Lowlands. Temperatures recorded just north of Colton are, however, distinctly higher (694–758 °C). Although it is likely that the Popple Hill gneiss amphibolites experienced some effects of progressive metamorphism, particularly in the vicinity of Colton, the variations in modal mineralogy are most likely the result of such factors as local variations in the bulk chemistry of the protolith and in the fugacity of H₂O due to infiltration of diluting species (e.g. CO₂, CH₄), rather than a regional temperature variation. Temperatures recorded by the HPCQ geothermometer reported here are similar in magnitude and geographic trend to those reported for graphite–calcite carbon‐isotope thermometry by Kitchen & Valley (1995), suggesting that peak metamorphism in the Adirondack Lowlands involved laterally extensive and fairly uniform isotherms.     

Mantle-derived magmatic gas releasing features at the Rehai area, Tengchong county, Yunnan Province, China

This paper deals with the chemical and isotopic compositions of escaped gases from the Rehai geothermal area in Tengchong county of Yunnan Province. Results indicate that there is the mantle-derived magmatic intrusion in shallow crust at this area. Modern mantle-derived magmatic volatiles are being released currently in a steady stream by way of active faults. The escaped gases are mostly composed of CO₂, together with subordinate amounts of H₂S, N₂, H₂, CH₄, SO₂, CO and He. At the studied area, the north-south directed fault is the deepest, and it may be interlinked with the deep-seated thermal reservoir that would be directly recharged by the mantle-derived magmatic volatile. The He, C isotopic evidence reveals that the modern active magma beneath Rehai area may originate from the historical mantle-derived magma which caused the latest eruptive activity of volcanoes in that region.     

Provenance of sandstones from the Wakino Subgroup of the Lower Cretaceous Kanmon Group, northern Kyushu, Japan

Abstract The Wakino Subgroup is a lower stratigraphic unit of the Lower Cretaceous Kanmon Group. Previous studies on provenance of Wakino sediments have mainly concentrated on either petrography of major framework grains or bulk rock geochemistry of shales. This study addresses the provenance of the Wakino sandstones by integrating the petrographic, bulk rock geochemistry, and mineral chemistry approaches. The proportions of framework grains of the Wakino sandstones suggest derivation from either a single geologically heterogeneous source terrane or multiple source areas. Major source lithologies are granitic rocks and high‐grade metamorphic rocks but notable amounts of detritus were also derived from felsic, intermediate and mafic volcanic rocks, older sedimentary rocks, and ophiolitic rocks. The heavy mineral assemblage include, in order of decreasing abundance: opaque minerals (ilmenite and magnetite with minor rutile), zircon, garnet, chromian spinel, aluminum silicate mineral (probably andalusite), rutile, epidote, tourmaline and pyroxene. Zircon morphology suggests its derivation from granitic rocks. Chemistry of chromian spinel indicates that the chromian spinel grains were derived from the ultramafic cumulate member of an ophiolite suite. Garnet and ilmenite chemistry suggests their derivation from metamorphic rocks of the epidote‐amphibolite to upper amphibolite facies though other source rocks cannot be discounted entirely. Major and trace element data for the Wakino sediments suggest their derivation from igneous and/or metamorphic rocks of felsic composition. The major element compositions suggest that the type of tectonic environment was of an active continental margin. The trace element data indicate that the sediments were derived from crustal rocks with a minor contribution from mantle‐derived rocks. The trace element data further suggest that recycled sedimentary rocks are not major contributors of detritus. It appears that the granitic and metamorphic rocks of the Precambrian Ryongnam Massif in South Korea were the major contributors of detritus to the Wakino basin. A minor but significant amount of detritus was derived from the basement rocks of the Akiyoshi and Sangun Terrane. The chromian spinel appears to have been derived from a missing terrane though the ultramafic rocks in the Ogcheon Belt cannot be discounted.     

Geochemical mass balance and weathering rates of ultramafic schists in Amazonia

The hydrochemical balance of the Yaou catchment in French Guiana was determined over a period of 1 year, combined with a detailed characterization of the primary minerals and their weathering products, in order to estimate ultramafic rock weathering rates in a rainforest environment. The time required to develop the main horizons of the laterite profile was obtained from estimations of the weathering rates and dissolution kinetics of some major parent minerals (chlorite, serpentine, biotite, calcite).

The specific transport of solute matter in the catchment is 205 kg/ha/a. The Cl and NO₃ net outputs shows that the system is in dynamic equilibrium, notably with respect to the biomass reservoir. The output flux of Mg in solution is mainly supplied from the weathering of primary minerals, whereas that of Ca comes both from atmospheric contributions and from the dissolution of carbonates. The fluxes of K and, more particularly, Na derive essentially from the atmosphere. Knowing the weathering rate of primary minerals, the total CO₂ consumption rate by silicate weathering is estimated at 1430 mol/ha/a.

The weathering rates of chlorite, serpentine and biotite range from 18 to 65 mol/ha/a, and those of talc and calcite are, respectively 51 and 153 mol/ha/a. Weathering rates normalized to mineral modal proportions give a decreasing order of stability resistance to weathering (calcitebiotitechlorite>serpentine>talc) that agrees with their vertical distribution in the weathering profile. The dissolution kinetics of chlorite, biotite and serpentine, expressed in relation to the Si release rate, were calculated using estimations of the mineral exchange surface by (a) optical microscope image processing of crystal outlines, and (b) BET specific surface measurements. The release rate of Si, computed for biotite, chlorite and serpentine, ranges around 10⁻¹³ and 10⁻¹⁴ mol/m²/s using microscope images on particle sizes. The estimated dissolution kinetics is two orders of magnitude lower when using the BET measured exchange surface, which is 100 times larger.

The saprolitization rate, calculated from the weathering rates of calcite, chlorite and biotite, is on average 7.5 m/Ma. The rate of latosol development, calculated from the weathering rate of serpentine at the saprolite–latosol interface, is estimated at 4.5 m/Ma. That means that the profile is chemically thickening at a rate of 3 m/Ma.