Chemical Weathering and CO2 Consumption of Chishuihe River Basin,Guizhou Province

Carbon sink produced during rock weathering is critical to global carbon cycles. In this work, we analyzed the major ion chemistry of the Chishuihe River Basin, and the major ion composition of the Chishuihe River system and the principal component analysis was applied for estimating the weathering rate and atmospheric CO₂ consumption via the rock chemical weathering. The results demonstrated that the chemical composition of the river was dominated by Ca²⁺, Mg²⁺, HC and S. The average concentration(317.88 mg/L) of the total dissolved solids within the Chishuihe River was higher than the average value (65 mg/L) of world rivers. The Gibbs graph combining major ion element ratio analysis indicated that the catchment major ion composition mainly originated from rock weathering, primarily from carbonate weathering, sparsely from silicate weathering. Carbonate and silicate weathering contributed 70.77% and 5.03% separately to the dissolved loads. The anthropogenic and precipitation impact was limited. According to calculation based on principal component and the ion composition characteristics, the chemical weathering rate was 126.716 t/(km²·a), significantly higher than that of the Yellow River and Yangtze River, and also higher than the average rate of the global major rivers. The CO₂ consumption flux based on annual average runoff was 10.96×10⁹ mol/a, and the CO₂ consumption rate by chemical weathering was 5.79×10⁵ mol/(km²·a).     

黄渤海有机碳的分布特征及收支评估研究

陆架边缘海是陆海相互作用研究中最为关键的区域,也是全球重要的碳储库,在区域物质循环过程中发挥着重要的作用。基于2012年5月和11月对黄渤海海域的综合调查,对该海域水体和沉积物中有机碳的含量与分布进行了分析,并结合相关文献资料对黄渤海有机碳的收支进行了估算。主要结论为:黄渤海溶解有机碳和颗粒有机碳均呈近岸河口区域高、离岸低的分布趋势;有机碳的组成以溶解有机碳为主,颗粒有机碳由海洋自生的有机碳和陆地来源的有机碳组成;黄渤海沉积物有机碳高值区主要分布在河口和泥质区,其组成也是由海洋自生和陆源混合而成,其中渤海以陆源为主,而黄海以海源为主。黄渤海有机碳收支评估表明,有机碳的主要来源为初级生产力产生的有机物,其贡献为(6 760±971)×104t/a,占有机碳输入总量的(74±10)%,沉积物再悬浮的通量为(884±200)×104t/a,东海向黄海输入的通量为(679±107)×104t/a,河流及陆源输入的通量为(643±63)×104t/a,大气干湿沉降的通量为(141±39)×104t/a,其贡献分别占有机碳输入总量的(10±2.2)%,(7.5±1.2)%,(7.0±0.7)%和(1.5±0.4)%;黄渤海有机碳的主要支出为呼吸消耗,其贡献为(5 190±746)×104t/a,占有机碳输出总量的(57±8.2)%,黄海向东海输出的通量为(2 150±370)×104t/a,有机碳沉积通量为(1 030±225)×104t/a,有机碳降解通量为(737±191)×104t/a,其贡献分别占有机碳输出总量的(24±4.1)%,(11±2.5)%和(8.0±2.1)%。有机碳收支评估表明黄渤海有机碳以海洋自生来源为主,且具有潜在碳的"汇"的特性,水体中外源输入和海洋自生有机碳的(1.6±0.3)%埋藏于该海域内。     

天津平原区浅层地下水水化学特征及碳酸盐风化碳汇研究

大气 CO₂浓度在控制全球气候变化方面具有至关重要的作用,研究碳循环、CO₂收支平衡和精确评估是制定区域CO₂减排策略和寻找新的碳汇途径最重要的组成部分。碳酸盐风化碳汇是全球碳循环研究的一个重要方向。为此,本研究以天津平原区浅层地下水为研究对象,通过对地下水调查及水样的采集与分析,运用水化学分析方法分析了地下水水化学特征,并估算了地下水总储存量、DIC储量和碳酸盐风化碳汇量。研究结果表明:浅层地下水化学场自北部山前平原向南部冲积平原和滨海平原,呈现出自北而南和由北西向南东的水平水化学分带规律,地下水由低浓度的淡水、微咸水变为高浓度咸水,沿此方向水化学类型由HCO₃-Ca·Na·Mg→Cl·SO₄-Na→Cl·HCO₃-Na→Cl-Na型转变;淡水区、微咸水区和咸水区面积分别为733、3 034和6 564 km²。地下水水化学组分中Ca²⁺、Mg²⁺和 {\mathrm{HCO}}_3^{-}主要来源于碳酸盐的溶解作用。研究区浅层地下水总储存量为2 241 640万m³,总DIC储量为8.13×10⁶ t,总碳汇量为4.11×10⁶ t。研究区浅层地下水淡水区、微咸水区和咸水区地下水储存量分别为157 799万、6 245 936万和1 459 247万 m³,DIC浓度分别为19200、19200和19342 mg/L,DIC储量分别为0.67×10⁶、1.65×10⁶和0.58×10⁶ t,碳汇量分别为0.22×10⁶、0.90×10⁶和2.98×10⁶ t。沿地下水流向,DIC、储量和碳汇量的空间分布均呈现出由低到高的趋势。     

气候变化的“地心说”——关于短期气候预测的新思维

通过对短期气候观测研究历史的回顾，提出了建立以“地圈”（包括地壳、地幔、地核）为主体的地气耦合模式，用来作为预测短期气候变化的方法。地球系统各子系统中，地圈的质量是水圈的１０＾３倍，是气圈的１０＾６倍，是生物圈的１０＾８倍。亦即整个地球系统中９９％以上的质量集中在地圈中。“地圈”（特别是岩石圈）存在着各种时间尺度的变化，所有这些变化必然影响到大气圈。对大气中≤１０＾－２年的波动，大气圈本身的能耗水     

寒冻风化控制的祁连山风化碎屑的空间分布

寒冻风化是冰缘地貌区及高寒山区的主要物理风化过程,其提供的风化碎屑物质是该区域崩塌等灾害性地貌过程的主要物质来源。由于寒冻风化对基岩的破碎是由温度控制的累积过程,过去温度变化对地貌演化具有重要意义,但其时间尺度的选取尚需进一步探究。因此本文选取祁连山北部为研究区,通过对比分析风化碎屑的空间分布特征与不同时间尺度温度变化控制的平均寒冻风化强度的空间分布特征,探讨干旱半干旱高寒山区风化碎屑空间分布的主要控制因素。结果显示,万年尺度及十万年尺度平均寒冻风化强度的高值与风化碎屑边界存在较好的空间一致性,祁连山西段万年尺度平均寒冻风化强度的高值与风化碎屑边界的空间相关性优于十万年尺度。本研究同时指出,温度升高导致寒冻风化的作用区向高海拔区域移动,进而产生新的高风险灾害区域。本研究强调寒冻风化对灾害性地貌过程的调控作用,为全球变暖背景下灾害性地貌过程的预测提供了新的思路,可以成为防灾减灾决策的重要参考。     

全球变暖背景下北美育空河流域化学风化增强

硅酸盐岩风化对气候变化和构造运动的反馈对长尺度气候变化可能起到重要的调节作用,对该反馈过程的定量认识有助于更确切理解地球碳循环的运行规律。通常认为风化类型可分为两种,分别是供应限制和动力学限制。全球变暖可能促进了动力学限制流域的化学风化作用,然而,关于这方面的认识仍很有限。育空河流域是典型的动力学限制风化区域,研究育空河的风化对气候变暖的响应有助于深入认识气候和大陆风化之间的相互作用。正演模型是区分河流风化端元的重要手段,文章利用正演模型对育空河流域从1975年到2019年的主要离子组成的数据集进行分析,并获得了该流域在过去几十年的化学风化速率的变化趋势。结果表明,育空河水化学性质主要受到碳酸盐岩风化和硅酸盐岩风化控制,两者多年平均碳汇通量分别为2.1×10¹¹ mol/yr和4.1×10¹⁰ mol/yr,处于世界主要大河碳汇通量的中间水平。更重要的是,在同一时期,伴随着2.2℃的温度增幅和13.7%的径流量增加,流域内的阳离子总通量增加了35.7%,其中硅酸盐岩和碳酸盐岩风化产生的阳离子通量分别增加了41%和35%,阳离子通量/风化速率对气候的敏感性与冰岛地区的研究结果符合的很好,与风化速率加快相对应的,硅酸盐岩风化碳汇通量相对增加了59.6%。尽管碳汇的增加在绝对通量上相比人类化石燃烧产生的碳排放通量微不足道,但是考虑到构造尺度内全球硅酸盐岩风化速率的增强,尤其是在较为寒冷的高纬度地区,额外的二氧化碳固定量可能对地球历史时期的全球气候产生重要影响。     

普定岩溶水-碳循环模拟试验场水体双碳同位素特征(δ13C-Δ14C)与碳足迹

河流输送到海洋的溶解无机碳(DIC)和有机碳(OC)受自然和人为双重因素的影响。了解DIC和OC的年龄、来源和转化,有助于掌握全球碳收支和提高现在以及未来自然和人类对河流碳循环影响的估算精度。本研究以普定岩溶水-碳循环试验场泉(地下水)-池(地表水)耦联系统为研究对象,利用双碳同位素(¹³C- ¹⁴C)方法,结合水生植物生长和传统水文地球化学特征,揭示了地下水-地表水系统中DIC和颗粒有机碳(POC)的来源及其转化机制。研究发现:(1)泉-池系统中DIC和POC的Δ¹⁴C具有相同的变化趋势,泉水中Δ¹⁴C值低于池水中Δ¹⁴C值,反映后者可能有“较年轻”的CO₂的加入;(2)池水水化学和碳同位素变化由土地利用类型和池中水生植物共同控制;(3)池水中颗粒有机碳(POC)浓度明显高于泉水,且其Δ¹⁴C值表现出与沉水植物和DIC的一致性(表观年龄均为3 200900 a),说明池水POC主要源于池中水生植物光合作用利用了碳酸盐风化产生的老碳(DIC),使新形成的有机质在表观年龄上“偏老”;(4)池水水体内源有机碳对水体POC的贡献在75%以上,内源有机碳通量(以C计)在250 t·km^-2·a^-1至660 t·km^-2·a^-1之间,相对于其他土地利用类型,草地对应的地表水系统具有最大的内源有机碳占比和通量,指示了沉水植物控制型浅水水体初级生产对有机碳循环的重要作用。综上,我们认为在岩溶区通过土地利用调整来调控水生植物群落对于增加碳汇具有重要潜力。     

Study on the Soil Carbon Pool and Potential Capacity of Carbon Sequestration in the Northern Tibetan Plateau

It is important to investigate the soil organic carbon reserves of the northern Tibetan Plateau for understanding the global carbon cycle. The surface soil carbon storage is 1.27×10⁸ t, and the surface topsoil organic carbon density is 4.96×10³ t/km² in the study area. Compared with the results of the second National Soil Census, the distribution of organic carbon reserves of chestnut soil, sierozem, alpine steppe soil, swamp soil, sandy soil and ustic cambisols increased gradually, which are mainly distributed in savanes of the northern Qinghai Lake and woodland in middle-high mountain areas of the eastern Qinghai Lake; savanes and woodland are classified as the carbon sink area because this area’s carbon sequestration is greater than the release quantity. By contrast, the distribution of organic carbon reserves of mountain meadow soil, alpine meadow soil, grey cinnamon soil, chernozem and anthropogenic-alluvial soil decreased gradually, which are mainly distributed in the farming areas of eastern Qinghai Province. This area’s carbon sequestration is less than the release quantity because of cultivation effect, and is classified as the carbon source area. The 97.5% of organic carbon storage cumulative frequency is closed to the threshold value of the organic carbon saturation. The carbon sequestration potential of the study area is 241.57×10⁶ t. Take the widely distributed chestnut soil as a case, it will take 18.66 years to reach saturation for the soil organic carbon reserves of chestnut soil.     

岩溶试片的岩性差异对估算岩溶速率和碳通量的影响

研究岩性差异对溶蚀速率的影响有助于提高溶蚀试片法估算岩溶碳汇强度的精确度。本文以贵州省普定县为研究区,将埋放地的主要基岩类型（石灰岩与白云岩）制成标准尺寸的试片,并将其埋设于不同土地利用类型和土壤深度下,经过4个水文年的监测后将估算的结果与前人在同一区域使用标准溶蚀试片的研究结果进行对比分析,结果表明:（1）在相同气候和土壤环境条件下,岩性对溶蚀试片的溶蚀速率有显著影响,且溶蚀速率与岩石中CaO含量呈正相关关系,与MgO含量呈负相关关系;（2）石灰岩与白云岩试片溶蚀速率的差异程度受土地利用及埋放深度的调控,整体上石灰岩溶蚀速率比白云岩溶蚀速率大14%;（3）不同岩性试片估算的岩溶碳汇强度相差较大,标准溶蚀试片估算的结果比埋放地基岩试片估算的结果高。故使用溶蚀试片法估算区域岩溶碳通量时应考虑埋放地基岩的岩性,或者对基于标准溶蚀试片的估算结果进行校正,才能准确反映区域尺度真实的岩溶碳通量大小。      

青藏高原草地土壤有机碳库及其全球意义

定量分析了青藏高原各类草地0～0.65m深度范围内有机碳储量,结果表明:青藏高原总面积为1.6027×10hm²的草地有机碳量达到335.1973×10⁸tC,其中以高原草甸土和高原草原土有机碳积累量为主,两者之和达到232.36×10⁸tC,占全国土壤有机碳量的23.44%,是全球土壤碳库的2.4%.在有机碳储量分析的基础上,按土壤碳释放的两种主要途径:土壤呼吸作用和土地利用方式变化与草地退化,对草地土壤碳排放进行了估算,揭示出青藏高原草地土壤通过呼吸每年排放的CO₂达到11.7×10⁸tC·a^-1,约占中国土壤呼吸总量的2.3%,明显高于全国乃至全球平均值;近30a来,青藏高原草地土壤由于土地利用变化和草地退化所释放的CO₂估计约有30.23×10⁸tC.保护青藏高原草地对于全球变化意义重大.定量分析了青藏高原各类草地0～0.65m深度范围内有机碳储量,结果表明:青藏高原总面积为1.6027×10hm²的草地有机碳量达到335.1973×10⁸tC,其中以高原草甸土和高原草原土有机碳积累量为主,两者之和达到232.36×10⁸tC,占全国土壤有机碳量的23.44%,是全球土壤碳库的2.4%.在有机碳储量分析的基础上,按土壤碳释放的两种主要途径:土壤呼吸作用和土地利用方式变化与草地退化,对草地土壤碳排放进行了估算,揭示出青藏高原草地土壤通过呼吸每年排放的CO₂达到11.7×10⁸tC·a^-1,约占中国土壤呼吸总量的2.3%,明显高于全国乃至全球平均值;近30a来,青藏高原草地土壤由于土地利用变化和草地退化所释放的CO₂估计约有30.23×10⁸tC.保护青藏高原草地对于全球变化意义重大.     

A reevaluation of the oceanic uranium budget for the Holocene

We present a new assessment of the pre-anthropogenic U budget for the Holocene ocean. We find that the gross input of U to the ocean lies in the range 53±17 Mmol/year, where the dominant source is river runoff (42.0±14.5 Mmol/year) and the direct discharge of groundwater could represent a significant additional input (9.3±8.7 Mmol/year). The soluble U flux associated with the aeolian input of crustal dust is minor (1.8±1.1 Mmol/year), falling well within the errors associated with the riverine flux. Removal of U to the organic rich sediments of salt marshes and mangrove swamps during river–sea mixing may significantly modify the riverine flux, such that the net U input is reduced to 42±18 Mmol/year. Evaluation of the U isotope budget demonstrates that the limits we have established on the U input flux are reasonable and suggests that direct groundwater discharge may play a significant role in maintaining the oceanic excess of ²³⁴U. The total sink of U from the ocean lies in the range 48±14 Mmol/year. We find that three major processes control the magnitude of this flux: (1) removal to oxygen-depleted sediments (26.9±12.2 Mmol/year); (2) incorporation into biogenic carbonate (13.3±5.6 Mmol/year); and (3) crustal sequestration during hydrothermal alteration and seafloor weathering (5.7±3.3 Mmol/year). The removal of U to opaline silica (0.6±0.3 Mmol/year) and hydrogenous phases (1.4±0.8 Mmol/year) is minimal, falling well within the errors associated with the other sinks. That the input and output fluxes balance within the calculated errors implies that U may be in steady state in the Holocene ocean. In this case, the input and output fluxes lie in the range 34–60 Mmol/year, giving an oceanic U residence time of 3.2–5.6×10⁵ years. However, given the large uncertainties, a significant imbalance between the Holocene input and output fluxes cannot be ruled out. The constancy of the ancient seawater U concentration implies that the U budget is in steady state over the time period of a glacial–interglacial climate cycle (10⁵ year). A Holocene flux imbalance must, therefore, be offset by an opposing flux imbalance during glacial periods or at the interglacial–glacial transition. We suggest that the storage of U in the coastal zone and shallow water carbonates during interglacial periods and the release of that U at or following the interglacial–glacial transition could be sufficient to affect the short-term stability of the U budget. Providing tighter constraints on U fluxes in the Holocene ocean is a prerequisite to understanding the U budget on the time scale of a glacial–interglacial climate cycle and using this element as a valuable palaeoceanographic proxy.     

Advances in Study of Phytolith Carbon Sequestration in Terrestrial Ecosystems of China

Phytolith-Occluded Carbon (PhytOC), a relatively stable carbon fraction, plays an important role in biogeochemical carbon cycle and mitigation of global warming. The formation mechanisms of PhytOC, the influence factors of phytolith carbon sequestration, the advances in study of phytolith carbon sequestration, and the management for enhancing the potential of phytolith carbon sequestration in terrestrial ecosystems of China were summarized in this review. Finally, future researches on phytolith carbon sequestration in terrestrial ecosystems of China were prospected. Climates, vegetation types, soil circumstances, the chemical compositions of the phytoliths and other factors will directly or indirectly affect the potential of phytolith carbon sequestration. In China, the PhytOC production quantity in grassland, cropland, forest, wetland and shrub ecosystems is (0.6±0.1)×10⁶,(4.9±1.7)×10⁶,(1.9±0.4)×10⁶,(0.6±0.5)×10⁶ and (1.3±0.3)×10⁶ t CO₂/a, respectively. Application of silicon-containing fertilizer, cultivation of high-silicon plant, and traditional enhancement of the plant net primary productivity can significantly improve the potential of phytolith carbon sequestration in terrestrial ecosystems of China. Future studies should focus more on ①the mechanisms of phytolith formation in different plants, ②the phytolith carbon sequestration in underground parts of plants from different terrestrial ecosystems, ③the quantification of soil PhytOC in different terrestrial ecosystems. Furthermore, more comprehensive, economical and reasonable management practices of improving the potential of phytolith carbon sequestration should also be further studied in different terrestrial ecosystems.     

Gum rosin (colophony): A suitable material for thermomechanical modelling of the lithosphere

We investigate the use of a ductile material with temperature-sensitive viscosity for thermomechanical modelling of the lithosphere. First, we consider the scaling of mechanical and thermal properties. For a normal field of gravity, the balance of stresses and body forces sets the stress scale, in proportion to the linear dimensions and the densities. The equation of thermal conduction sets the time scale. The activation enthalpy for creep sets the temperature scale; but the thermal expansivity provides an additional constraint on this temperature scale.

Gum rosin appears to be a suitable material for lithospheric modelling. We have measured its flow properties, at various temperatures, in a specially designed rotary viscometer with unusually low machine friction. The rosin is almost Newtonian. Strain rate depends upon stress to the power n, where 1.0 <n < 1.14. The viscosity varies over 5 orders of magnitude, from about 10² Pa s at 80°C, to about 10⁷ Pa s at 40°C. The activation enthalphy is thus about 250 kJ/mol. Measured with a needle probe, the thermal conductivity is 0.113 ± 0.001 W m⁻¹K⁻¹; the thermal diffusivity, (6±3) ×10⁻⁷ m² s⁻¹. Calculated from X-ray profiles, the thermal expansivity is about 3 × 10⁻⁴ K⁻¹. These thermal and mechanical properties make gum rosin suitable for thermomechanical models, where linear dimensions scale down by a factor of 10⁶; time, by 10¹¹; viscosity, by 10¹⁷; and temperature change, by 10¹.     

塔里木西南缘布雅花岗岩体地球化学特征及构造意义

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格尔木河222Rn同位素变化及其对地表水-地下水交互关系的指示意义

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土地利用变化对高寒草甸土壤有机质更新的影响

对青藏高原海北站区的自然土壤和扰动土壤进行高分辨率采样,测定土壤根系、有机碳及其¹⁴C含量;用¹⁴C示踪技术探讨土地利用变化对高寒草甸土壤有机质更新的影响.研究表明,土地利用变化对高寒草甸土壤碳循环影响显著.耕作活动导致扰动土壤有机碳储量比自然土壤增加29.35%;扰动土壤剖面10~50 cm深土壤有机质的¹⁴C含量相对富集;自然土壤大多数有机碳储存在土壤表层,更新时间<50 a,同一深度扰动土壤有机碳储量显著少,更新时间长(171~294 a);自然土壤10 cm以下有机碳主要为更新时间>1 000 a的稳定碳所控制,扰动土壤的相应值出现在40 cm以下;自然土壤有机质更新产生的CO₂通量为114 gC·m^-2·a^-1,扰动土壤为48.7 gC·m^-2·a^-1.     

古地下水定年新方法——81Kr法

由于⁸¹Kr化学性质稳定、半衰期长且在地下水运移过程中没有额外来源的优点,近年来,成为测定古老地下水年龄（10⁵~10⁶ a）的有效手段.国外对于⁸¹Kr的测定方法、地下水定年应用研究已较为深入,而国内应用⁸¹Kr作为水文地质学的研究尚处于起步阶段.本文通过对国内外⁸¹Kr应用于地下水测年的原理以及⁸¹Kr的测定方法进行总结,针对目前研究的问题进行探讨,并对今后放射性氪核素在水文地球化学中的研究进行展望,为国内对于⁸¹Kr的测定与在古地下水定年研究方面提供科学依据.     

库鲁克塔格兴地塔格群变质石英岩复杂锆石特征及指示意义

造山带内造山作用时限的划分是识别超大陆的重要依据.为找寻库鲁克塔格古元古代晚期造山作用与锆石微区特征间的联系,运用LA-ICP-MS技术分析了石英岩中64个锆石U-Pb同位素点.结果显示:∑REE=47×10-6～490×10-6(40个点,下同),570×10-6～1384×10-6(24);Th/U＜0.4(33)...     

江西香炉山钨矿床矽卡岩矿物和成矿花岗岩地球化学特征及其指示意义

江西香炉山大型钨矿床位于长江中下游成矿带南侧新识别的钨矿带西段,为一矽卡岩型白钨矿床.矽卡岩矿体主要产于中寒武统杨柳岗组含炭质灰岩和香炉山花岗岩接触部位.香炉山花岗岩具有细粒至中粗粒结构,主要由石英、钾长石、斜长石和黑云母组成,副矿物以钛铁矿为主.香炉山花岗岩的SiO2含量为66.37％～67.76％,并具有较高的Na...     

峨眉山玄武岩化学风化研究——以龙苍沟小流域为例

通过对四川省雅安龙苍沟峨眉山玄武岩小流域的水化学组成研究,分析了不同物质来源对小流域溪水溶解质的贡献,并对该小流域岩石风化速率和CO2消耗速率进行了估算。结果表明,龙苍沟流域溪水呈中性,PH平均值为6.82。溪水中阳离子以Ca^2+为主,约占阳离子总量的56%;阴离子以HCO3^-为主,约占阴离子总量的45%。碳酸盐岩风化、硅酸盐岩风化、大气降水和人为活动对溪水阳离子平均贡献率分别为50.2%、38.2%、10.5%和1.1%。流域硅酸盐岩风化速率为37.54±24.94 t/km^2/yr,硅酸盐岩风化对大气C02消耗速率为5.4±3.6 mol C/km^2/yr。本文首次对我国峨眉山玄武岩省化学风化大气CO2消耗量进行估算,得到其年消耗通量为1.35±0.89×10^11 mol C/yr,约为全球玄武岩CO2年消耗通量的3.31±2.18%。