Profondeur d'extraction racinaire et signature isotopique de l'eau prélevée par les racines des couverts végétaux

We seek to identify the depth to which water is extracted by the roots in the soil. Indeed, in an isotopic steady-state condition of leaf water, transpiration introduces into the atmosphere a vapour whose isotopic signature is identical to that of root water. In the isotopic models of atmospheric general circulation, it is classically allowed that the signature of transpiration belongs to the meteoric water line. This supposes that the water taken by the roots has escaped with the evaporation of the soil and comes thus from the deep layers of the soil. At the time of experimentation carried out on maize plants (Nemours, Seine-et-Marne, France), this extraction depth was inferred from the comparison between the signature of the water measured on the level of the first internode of the stems of the plants and the isotopic profile of water in the soil. When the flow of transpiration reaches a maximum value, the plant uptakes water resulting from precipitations and which preserves its non-evaporating character after having quickly infiltrated in the deep layers of the soil. This relates to only 55% of the flux transpired by the canopy, the remainder presenting an evaporating character more or less marked according to ambient conditions. This experiment invalidates the classical hypothesis used in isotopic models of general atmospheric circulation in temperate regions. In fact, only half the amount of water vapour transpired by the canopy during the day presents a signature similar to that of the rainwater sampled in deep soil layers. To cite this article: Z. Boujamlaoui et al., C. R. Geoscience 337 (2005).     

Zircon U–Pb ages and Hf isotope compositions of migmatites from the North Qinling terrane and their geological implications

Migmatites are predominant in the North Qinling (NQ) orogen, but their formation ages are poorly constrained. This paper presents a combined study of cathodoluminescence imaging, U–Pb age, trace element and Hf isotopes of zircon in migmatites from the NQ unit. In the migmatites, most zircon grains occur as new, homogeneous crystals, while some are present as overgrowth rims around inherited cores. Morphological and trace element features suggest that the zircon crystals are metamorphic and formed during partial melting. The inherited cores have oscillatory zoning and yield U–Pb ages of c. 900 Ma, representing their protolith ages. The early Neoproterozoic protoliths probably formed in an active continental margin, being a response to the assembly of the supercontinent Rodinia. The migmatite zircon yields Hf model ages of 1911 ± 20 to 990 ± 22 Ma, indicating that the protoliths were derived from reworking of Palaeoproterozoic to Neoproterozoic crustal materials. The anatexis zircon yields formation ages ranging from 455 ± 5 to 420 ± 4 Ma, with a peak at c. 435 Ma. Combined with previous results, we suggest that the migmatization of the NQ terrane occurred at c. 455–400 Ma. The migmatization was c. 50 Ma later than the c. 490 Ma ultra‐high‐P (UHP) metamorphism, indicating that they occurred in two independent tectonic events. By contrast, the migmatization was coeval with the granulite facies metamorphism and the granitic magmatism in the NQ unit, which collectively argue for their formation due to the northward subduction of the Shangdan Ocean. UHP rocks were distributed mainly along the northern margin and occasionally in the inner part of the NQ unit, indicating that they were exhumed along the northern edge and detached from the basement by the subsequent migmatization process.     

Dissolved organic matter in surface runoff in the Loess Plateau of China: The role of rainfall events and land-use

Exploring the chemical characterization of dissolved organic matter (DOM) is important for understanding the fate of laterally transported organic matter in watersheds. We hypothesized that differences in water-extractable organic matter (WEOM) in soils of varying land uses and rainfall events may significantly affect the quality and the quantity of stream DOM. To test our hypotheses, characteristics of rainfall-runoff DOM and WEOM of source materials (topsoil from different land uses and gullies, as well as typical vegetation) were investigated at two adjacent catchments in the Loess Plateau of China, using ultraviolet–visible absorbance and excitation emission matrix fluorescence with parallel factor analysis (PARAFAC). Results indicated that land-use types may significantly affect the chemical composition of soil WEOM, including its aromaticity, molecular weight, and degree of humification. The PARAFAC analysis demonstrated that the soils and stream water were dominated by terrestrial/allochthonous humic-like substances and microbial transformable humic-like fluorophores. Shifts in the fluorescence properties of stream DOM suggested a pronounced change in the relative proportion of allochthonous versus autochthonous material under different rainfall patterns and land uses. For example, high proportions of forestland could provide more allochthonous DOM input. This study highlights the relevance of soils and hydrological dynamics on the composition and fluxes of DOM issuing from watersheds. The composition of DOM in soils was influenced by land-use type. Precipitation patterns influenced the proportion of terrestrial versus microbial origins of DOM in surface runoff. Contributions of allochthonous, terrestrially derived DOM inputs were highest from forested landscapes.     

Direct dating of folding events by 40Ar/39Ar analysis of synkinematic muscovite from flexural-slip planes

Timing of folding is usually dated indirectly, with limited isotopic dating studies reported in the literature. The present study investigated the timing of intracontinental, multi-stage folding in Upper Proterozoic sandstone, limestone, and marble near Beijing, North China, and adjacent regions. Detailed field investigations with microstructural, backscattered electron (BSE) images and electron microprobe analyses indicate that authigenic muscovite and sericite crystallized parallel to stretching lineations/striations or along thin flexural-slip surfaces, both developed during the complex deformation history of the study area, involving repeated compressional, extensional and strike-slip episodes. Muscovite/sericite separates from interlayer-slip surfaces along the limbs and from dilatant sites in the hinges of folded sandstones yield muscovite ⁴⁰Ar/³⁹Ar plateau ages of ∼158–159 Ma, whereas those from folded marble and limestone samples yield ages of 156 ± 1 Ma. Muscovite from thin flexural-slip planes on fold limbs and hinges yields ages within analytical error of ∼155–165 Ma. Further muscovite samples collected from extensionally folded limestone and strike-slip drag folds yield younger ages of 128–125 Ma with well-defined plateaus. To assess the potential influence of the detrital mica component of the host rock on the age data, two additional muscovite samples were investigated, one from a folded upper Proterozoic–Cambrian sandstone outside the Western Hills of Beijing and one from a folded sandstone sampled 20 cm from folding-related slip planes. Muscovite separates from these samples yield significantly older ages of 575 ± 2 Ma and 587 ± 2 Ma, suggesting that the timing of folding can be directly determined using the ⁴⁰Ar/³⁹Ar method. This approach enables the identification and dating of distinct deformation events that occur during multi-stage regional folding. ⁴⁰Ar/³⁹Ar dating can be used to constrain the timing of muscovite and sericite growth at moderate to low temperatures (<400 °C) during folding, yielding well-defined plateau ages and thereby the age of deformation in the upper crust.     

湖南宝山矿床花岗岩类硫-铅同位素和流体包裹体研究及其成因意义

宝山铜铅锌多金属矿床是湖南重要的铅锌生产基地。矿床内矽卡岩型铜(钼)矿化受侏罗纪花岗闪长斑岩的控制,而主要的铅锌矿体则产于远离岩体的碳酸盐地层中,且缺乏可靠的矿化年龄限制。为了查明宝山铅锌矿体与花岗闪长斑岩之间的成因关系,文章对宝山花岗岩类中浸染状黄铁矿的硫同位素和钾长石的铅同位素,以及铅锌矿石萤石脉石的流体包裹体进行了测试和研究,并与前人报道的铅锌硫化物矿石的硫、铅同位素进行了对比,尝试为宝山铅锌矿化的物质来源及成因提供依据。研究表明,花岗闪长斑岩中浸染状黄铁矿的δ34S值为+1.5‰~+3.5‰,与铅锌矿石硫化物(方铅矿、闪锌矿及黄铁矿)相一致;同时,花岗岩类中钾长石的铅同位素组成206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为18.4789~18.7668、15.6835~15.7220和38.7903~39.1035,具有壳源的特征,且与铅锌矿石硫化物的铅同位素分布范围相吻合。宝山矿床的硫、铅同位素特征表明,花岗闪长斑岩应是铅锌矿化的主要硫源及金属来源。宝山矿床铅锌矿石萤石中的流体包裹体具有低温(130~150℃)、低盐度(8%)的特征,可能是岩浆热液演化到晚期的产物。结合已有的有关资料加以对比和分析,研究认为,宝山铅锌矿床的成矿物质应来源于花岗闪长岩的岩浆期后热液,在热液演化晚期迁移到远端地层中沉淀,形成了宝山的主要铅锌矿体。     

准噶尔盆地东部沙帐地区中二叠统平地泉组一段致密油源储组合模式

综合利用录井、镜下薄片及压汞等资料,对准噶尔盆地东部沙帐地区中二叠统平地泉组一段致密油储集层岩性、储集空间和孔隙结构等特征进行了分析,在此基础上结合平一段致密油纵向岩性组合特征及源储关系,总结了平一段致密油源储组合模式。研究发现平一段致密油储集层岩性以碎屑岩为主,云质类岩石次之,储层孔隙结构具"粗态型"、"偏细态型"和"细态型",储集空间表现为常规孔隙与纳米孔隙并存;平一段源储组合表现为"泥包砂"、"砂包泥"和"砂泥互层"。研究表明:平一段储集层表现为致密储层特征,纳米孔喉是致密油储层的主体孔喉,平一段致密油具有源储一体型、源储交接型和源储隔离型三类组合模式。     

河南嵩县店房金矿区花岗斑岩锆石U-Pb年龄、Hf同位素及岩石地球化学

华北陆块南缘外方山店房金矿区内出露后沟、水漉塘和店房钾长花岗斑岩体(脉),其与隐爆角砾岩筒及金矿化有密切的空间关系。为查明钾长花岗斑岩体的侵位时代、岩石成因和源区性质,本次开展了锆石U-Pb定年、锆石Hf同位素及岩石地球化学分析等研究。结果表明岩体具有高硅、高钾、富铝、低镁的特征,属钾玄岩系列Ⅰ型花岗岩,轻重稀土元素分馏明显,具有弱的Eu负异常,岩石富集Rb、K、Ba等,亏损Nb、Ta、Sr、P、Ti等元素。锆石具有核—边结构,其中锆石边SHRIMP U-Pb年龄142.6±2.1Ma(MSWD=1.4),_(εHf)(t)=-23.0~-13.8,两阶段模式年龄主要集中于2075~2652 Ma;锆石核LA-ICPMS U-Pb年龄可分为两组,即2169~2336Ma和1732~1881Ma,Hf同位素组成可分为两组,_(εHf)(t)分别集中于-13.1~-4.8和-4.5~3.7,模式年龄主要集中于2376~2805Ma。表明钾长花岗斑岩体形成于142.6±2.1Ma的早白垩世早期,岩浆可能由2169~2336Ma的古老下地壳新太古代太华群部分熔融而成,并有地幔组分参与,岩浆在上升或定位过程中捕获了1732~1881Ma熊耳群火山岩的锆石。结合区域构造背景认为,该岩体是早白垩世古太平洋板块向欧亚大陆俯冲致使华北陆块岩石圈减薄伸展而引起的岩浆活动的产物。     

Iodine budget in surface waters from Atacama: Natural and anthropogenic iodine sources revealed by halogen geochemistry and iodine-129 isotopes

Iodine enrichment in the Atacama Desert of northern Chile is widespread and varies significantly between reservoirs, including nitrate-rich “caliche” soils, supergene Cu deposits and marine sedimentary rocks. Recent studies have suggested that groundwater has played a key role in the remobilization, transport and deposition of iodine in Atacama over scales of millions-of-years. However, and considering that natural waters are also anomalously enriched in iodine in the region, the relative source contributions of iodine in the waters and its extent of mixing remain unconstrained. In this study we provide new halogen data and isotopic ratios of iodine (¹²⁹I/I) in shallow seawater, rivers, salt lakes, cold and thermal spring water, rainwater and groundwater that help to constrain the relative influence of meteoric, marine and crustal sources in the Atacama waters. Iodine concentrations in surface and ground waters range between 0.35 μM and 26 μM in the Tarapacá region and between 0.25 μM and 48 μM in the Antofagasta region, and show strong enrichment when compared with seawater concentrations (I = ∼0.4 μM). In contrast, no bromine enrichment is detected (1.3–45.7 μM for Tarapacá and 1.7–87.4 μM for Antofagasta) relative to seawater (Br = ∼600 μM). These data, coupled to the high I/Cl and low Br/Cl ratios are indicative of an organic-rich sedimentary source (related with an “initial” fluid) that interacted with meteoric water to produce a mixed fluid, and preclude an exclusively seawater origin for iodine in Atacama natural waters. Iodine isotopic ratios (¹²⁹I/I) are consistent with halogen chemistry and confirm that most of the iodine present in natural waters derives from a deep initial fluid source (i.e., groundwater which has interacted with Jurassic marine basement), with variable influence of at least one atmospheric or meteoric source. Samples with the lowest isotopic ratios (¹²⁹I/I from ∼215 to ∼1000 × 10⁻¹⁵) strongly suggest mixing between the groundwater and iodine storage in organic-rich rocks (with variable influence of volcanic fluids) and pre-anthropogenic meteoric water, while samples with higher values (∼2000–93,700 × 10⁻¹⁵) indicate the input of anthropogenic meteoric fluid. Taking into account the geological, hydrologic and climatic features of the Atacama region, we propose that the mean contribution of anthropogenic ¹²⁹I is associated with ¹²⁹I releases during nuclear weapon tests carried out in the central Pacific Ocean until the mid 1990's (¹²⁹I/I = ∼12,000 × 10⁻¹⁵). This source reflects rapid redistribution of this radioisotope on a global scale. Our results support the notion of a long-lived continental iodine cycle in the hyperarid margin of western South America, which is driven by local hydrological and climate conditions, and confirm that groundwater was a key agent for iodine remobilization and formation of the extensive iodine-rich soils of Atacama.     

大湖塘矿集区燕山成矿阶段矿床成矿系列研究及找矿问题探讨

大湖塘矿集区位于赣西北九岭成矿带西北部位,区内燕山期岩浆岩侵入活动及成矿作用强烈。大湖塘燕山期岩浆岩形成时间分布在130.3 Ma~151.4 Ma之间,可划分为三次侵入:130.3 Ma~134.3 Ma、140.4 Ma~144.4 Ma、146.4 Ma~151.4 Ma;在144.4 Ma~146.4 Ma之间,岩浆活动处于休宁阶段。区内燕山期岩浆岩与矿床在形成时间上十分接近,空间关系上相互依存,并显示特定的分布格局。根据区内矿床的分布特点、产出位置、成矿时间、燕山期花岗岩与矿床的相关性等特征,可将大湖塘矿集区由北向南依次划分为W、Mo—W、Mo、Cu、Pb、Zn—Cu、Pb、Zn、Au、Ag三个成矿系列,并提出了"北钨南铜"的找矿观点。区内双桥山群与成矿,燕山期岩浆岩的起源,矿床等间距分布,以及重力勘探方面的研究应加强。