Research Progress in Responses of Modern Terrestrial Plant Carbon Isotope Composition to Climate Change

Global climate change has been one of the most concerned environmental problems in the world since the 1980s. Since stable carbon composition (¹³C) in plant tissues can record abundant information on climate changes, it has been widely used as an important climate proxy in global change studies and becomes a powerful tool for obtaining paleoclimate information, understanding paleoenvironment reconstruction and modern climate change, and predicting future climate trends. However, a lot of potential uncertainties have always involved in the reconstruction of paleoclimate and paleoenvironment by carbon isotope of the past period sediment or fossils. Among them, the most dominant uncertainty is due to our poor understanding of the relations between carbon isotope ratios of plants and climatic factors and the climatic and environmental significance indicated by modern plant ¹³C. This may limit the application of plant ¹³C in the study of climatic and environmental changes. Based on the Summary of plant ¹³C fractionation and carbon isotope distribution of different photosynthetic plants, the effects of environmental factors, e.g., temperature, precipitation, atmospheric CO₂ concentration, and altitude on terrestrial plant ¹³C and their relationships were reviewed in this paper, and the response mechanism of plant ¹³C to climate changes were also analyzed. Furthermore, the current existing problems and the future prospects in carbon isotope study were discussed. It is pointed out that strengthening some studies such as the response of C₄ plants ¹³C to climate environmental parameters, the transformation relation of different scale plant ¹³C, intersection and permeation of related disciplines, and various proxies and scientific method, will undoubtedly make us have a more accurate understanding of the climate history and eventually broaden the development of the field during the process of global change study by plant carbon isotope techniques.     

台风水汽稳定同位素组成与天气过程的关系——以2015 年13 号台风“苏迪罗”为例

基于台风“苏迪罗”（1513）影响前后南京实时高频监测的水汽稳定同位素数据,并结合再分析资料、HYSPLIT后向轨迹模型分析了大气水汽δ¹⁸O与天气过程之间的关系以及大气水汽过量氘所指示的水汽来源。结果表明,1）整个台风影响过程水汽δ¹⁸O先保持基本不变后一直下降的趋势,而水汽过量氘则呈现完全相反的变化趋势。2）根据台风“苏迪罗”影响前后南京水汽δ¹⁸O变化特征,将其划分为3个阶段：Ⅰ阶段水汽δ¹⁸O较高与南京地区较为稳定的大气条件相对应,水汽过量氘值较低指示南京地区主要受海洋水汽影响;Ⅱ阶段台风环流及其残压和北方南下冷空气相互作用造成南京地区强降水,水汽凝结和降雨蒸发的共同作用导致水汽δ¹⁸O不断贫化,较高的水汽过量氘表明南京地区主要受海洋和局地混合水汽的影响;Ⅲ阶段可能是中尺度下沉气流导致南京地区极端偏负的δ¹⁸O和高水汽过量氘。     

海进体系域碳氧同位素地球化学响应——以黔西南地区三叠系为例

层序地层研究表明,位于扬子地块西南缘的黔西南地区在中三叠世末期(相当于Ladinian-Carnian期)出现了一次与全球同步的大规模海侵,形成了一个向上变深的碳酸盐岩台地淹没沉积层序。垄头组顶部和竹竿坡组分别是海进体系域(TST)的下、上部分。碳、氧同位素研究表明,垄头组顶部自下而上δ(18O)持续增大,而δ(13C)先逐渐增大,后在顶部界面附近快速下降,反映了垄头组顶部在暴露环境下氧化作用的结果。竹竿坡组δ(13C)自下而上逐渐增大,δ(18O)总体呈现逐渐减小趋势,反映了海平面变化特征。研究认为,海进体系域的δ(13C)和δ(18O)演化不但反映了海平面和沉积环境变化,同时对密集段(CS)、层序界面和古暴露面等也有很好的识别作用,在层序地层研究中具有重要的意义。     

Groundwater geochemistry of the Chihuahua City region in the Rio Conchos Basin (northern Mexico) and implications for water resources management

The Chihuahua City region, located in the semiarid-arid northern highlands of Mexico, has experienced intensive groundwater abstraction during the last 40 years to meet water demands in the region. A geochemical survey was carried out to investigate the evolution from baseline to modern conditions of a 130-km flow path including the El Sauz–Chihuahua–Aldama–San Diego de Alcalá regions. The research approach included the use of major chemical elements, chlorofluorocarbons and environmental isotope (¹⁸O, ²H, ¹³C and ¹⁴C) tracers. Stable isotopes indicate that groundwater evolves from the evaporation of local rainfall and surface water. Groundwater located at the lower end of the flow section is up to 6000 years old and older groundwater in the order of 9000 years BP was found in a deep well located in the upper part of the flow system, implying contribution from a neighbour basin. The background groundwater chemistry upstream of Chihuahua City results from feldspar weathering. Beyond Chihuahua City the chemical conditions are strongly modified owing to disposal of sewage from public and industrial water supplies into the Rio Chuviscar, subsequent allocation of this water to agricultural irrigation areas and direct infiltration under the river bed. As a consequence, anions like chloride and sulphate are mainly related to surface sources. Nitrate is controlled in part by sewage from public supply and industry and in part by agricultural practices. Arsenic and fluoride are related to weathering of rock formations of local mineralized ranges and subsequent enrichment of the basin-fill by magmatic processes. The results of this study have implications for groundwater management in an arid region that depends entirely on groundwater for domestic, industrial and agricultural water consumption. Copyright © 2008 John Wiley & Sons, Ltd.     

Mineralogy of metal contaminated estuarine sediments,Derwent estuary,Hobart, Australia: implications for metal mobility

The mobility, bioaccessibility and transfer pathways of metals and metalloids in estuarine sediments have been the focus of much detailed research. However, to date, few studies have examined the mineralogical siting of metals and metalloids in such sediments. This is despite the fact the mineralogy of sediments is an important factor that controls which and how much of a particular metal is released to pore waters and overlying water columns. This study reports on the mineralogical siting of metals in contaminated estuarine sediments, Hobart, Australia, and aims to evaluate the mobility of metals in the contaminated substrates. Mineralogical, mineral chemical and bulk chemical analyses demonstrate that the sediments contain very high levels of several metals and metalloids. The contaminated sediments have concentrations of zinc (Zn), lead (Pb), copper (Cu) and cadmium (Cd) ranging from 0.55 to 4.23 wt%, 0.16 to 0.70 wt%, 415 to 951 mg/kg and 23 to 300 mg/kg, respectively. Franklinite and lesser sphalerite are the main repositories of Zn, whereas much of the Pb and Cu is hosted by sulfides, organic matter and undetermined iron (Fe) oxides. While the release of contaminant loads from franklinite through dissolution is likely to be insignificant, even small releases of metals from the highly contaminated sediments can still cause the deterioration of local water quality. The contaminated sediments represent long-term sources of metal pollutants, particularly Zn, to local waters. This study demonstrates that mineralogical analyses are a vital tool to recognise the potential mobility of trace metals in estuarine environments.     

A 24 h investigation of the hydrogeochemistry of baseflow and stormwater in an urban area impacted by mining: Butte,Montana

Changes in water quality during a storm event were continuously monitored over a 24 h period at a single location along an urban stormwater drain in Butte, Montana. The Butte Metro Storm Drain (MSD) collects groundwater baseflow and stormwater draining Butte Hill, a densely populated site that has been severely impacted by 130 years of mining, milling, and smelting of copper‐rich, polymetallic mineral deposits. On the afternoon of 26 June 2002, a heavy thunderstorm caused streamflow in the MSD to increase 100‐fold, from 0·2 ft³ s⁻¹ to more than 20 ft³ s⁻¹. Hourly discharge and water quality data were collected before, during, and following the storm. The most significant finding was that the calculated loads (grams per hour) of both dissolved and particulate copper passing down the MSD increased more than 100‐fold in the first hour following the storm, and remained elevated over baseline conditions for the remainder of the study period. Other metals, such as zinc, cadmium, and manganese, showed a decrease in load from pre‐storm to post‐storm conditions. In addition to the large flush of copper, loads of soluble phosphorus increased during the storm, whereas dissolved oxygen dropped to low levels (<2 mg l⁻¹). These results show that infrequent storm events in Butte have the potential to generate large volumes of runoff that exceed Montana water quality standards for acute exposure of aquatic life to copper, as well as depressed levels of dissolved oxygen. This study has important implications to ongoing reclamation activities in the upper Clark Fork Superfund site, particularly with respect to management of storm flow, and may be applicable to other watersheds impacted by mining activities. Copyright © 2005 John Wiley & Sons, Ltd.     

Copper‐gold mineralisation in New Guinea: Numerical modelling of collision,fluid flow and intrusion‐related hydrothermal systems

Two‐ and three‐dimensional numerical modelling techniques, constrained by key geodynamic data, provide insights into the controls on development of porphyry‐related Cu–Au mineralisation in the Tertiary collision zone of New Guinea. Modelling shows that the creation of local dilation to facilitate magma emplacement can be caused by reactivation of arc‐normal transfer faults, where they cut the weakened fold belt. Additionally, dilation occurs where fluid overpressuring is caused by collision‐related, south‐directed fluid flow being localised into the more permeable units of the Mesozoic passive‐margin sedimentary succession. Rapid uplift and erosion, which may be a mechanism for magmatic fluid release in these systems, is shown to be greatest in the west of West Papua, where the stronger Australian crust acts as a buttress. Within the Papuan Fold Belt, uplift is greatest near the margins, where the weaker fold belt abuts the stronger crust and/or major faults have been reactivated. Increased orographically induced precipitation and erosion exposes the lower parts of the stratigraphy within or on the margins of these uplifted zones. On a smaller scale, 2–D coupled fluid‐flow ‐ thermal‐chemical modelling uses a scenario of fluid mixing to calculate metal precipitation distribution and magnitude around an individual intrusive complex. Modelling highlights the interdependence of the spatial permeability structure, the regional temperature gradient, and the geometry of the convection cells and how this impacts on the distribution of metal precipitation.     

Metasomatic effects related to channelled fluid streaming through deep crust: fenites and associated carbonatites (In Ouzzal Proterozoic granulites, Hoggar, Algeria)

The In Ouzzal granulitic unit (IOGU) consists predominantly of felsic orthogneisses most of which correspond to granitoids emplaced during the Archaean, plus metasediments, including olivine-spinel marbles, of late Archaean age. All units were metamorphosed at granulite facies during the Eburnean (2 Ga). The stable isotope signature of the marbles (δ¹³C=–0.8 to –4.2‰/PDB; δ¹⁸O = 7.9 to 18.9‰/SMOW) does not record a massive streaming of C-bearing fluids during metamorphism. Most of the isotopic variation in the marbles is explained in terms of pregranulitic features. Metasomatic transformation of granulites into layered potassic syenitic rocks and emplacement of carbonate veins and breccias occurred during retrogressive granulite facies conditions. The chemistry of these rocks is comparable with that of fenites and carbonatites with high contents of (L)REEs, Th, U, F, C, Ba and Sr but, with respect to these elements, a relative depletion in Nb, Ta, Hf, Zr and Ti. The isotopic compositions of Nd (?Nd_(T)=–6.3 to –9.9), of Sr (⁸⁷Sr/⁸⁶Sr_(T)= 0.7093–0.7104), and the O isotopic composition of metasomatic clinopyroxene (δ¹⁸O = 6.9 to 8‰), all indicate that the fluid had a strong crustal imprint. On the basis of the C isotope ratios (δ¹³C =–3.5 to –9.7‰), the fluid responsible for the crystallization of carbonates and metasomatic alteration is thought to be derived from the mantle, presumably through degassing of mantle-derived magmas at depth. Intense interaction with the crust during the upward flow of the fluid may explain its chemical and isotopic signatures. The zones of metasomatic alteration in the In Ouzzal granulites may be the deep-seated equivalents of the zones of channelled circulation of carbonated fluids described at shallower levels in the crust.     

Geochemical and isotopic evidence of a groundwater source in the Corral Canyon meadow complex,central Nevada,USA

Major inorganic ions and stable carbon and oxygen isotopes in stream water, groundwater, groundwater seeps and springs were measured in the Corral Canyon meadow complex and watershed in the Toquima Mountains of central Nevada, USA. The purpose of the study was to determine whether stream water or groundwater was the source of water that supports vegetation in the meadow complex. Water samples from the watershed and meadow complex were mixed cation–HCO₃ type. Stream water sampled at different locations in the meadow complex showed variations in temperature, pH and specific conductance. The cation–anion proportions for stream water were similar to groundwater, groundwater seeps and runoff from the meadow complex. Stable oxygen isotope ratios for stream water (?17·1 to ?17·6‰ versus VSMOW) and groundwater and groundwater seeps in the meadow site (?17·0 to ?17·7‰ versus VSMOW) were similar, and consistent with a local meteoric origin. Dissolved inorganic carbon (DIC) and the δ ¹³C_DIC for stream water (?12·1 to ?15·0‰ versus VPDB) were different from that of groundwater from the meadow complex (?15·3 to ?19·9‰ versus VPDB), suggesting different carbon evolution pathways. However, a simple model based on cation–δ ¹³C_DIC suggests that stream water was being recharged by shallow groundwater, groundwater seeps and runoff from the meadow complex. This leads to the conclusion that the source of water that supports vegetation in the meadow complex was primarily groundwater. The results of this study suggest that multiple chemical and stable carbon isotope tracers are useful in determining the source of water that supports vegetation in meadow complexes in small alpine watersheds. Copyright © 2004 John Wiley & Sons, Ltd.     

Exhumation of a Variscan orogenic complex: insights into the composite granulitic–amphibolitic metamorphic basement of south-east Corsica (France)

A structural, petrological and geochronological (U‐Th‐Pb of zircon and monazite) study reveals that the lower crust sequences of the Variscan high‐grade basement cropping out between Solenzara and Porto Vecchio, south‐east Corsica (France) have been tectonically juxtaposed along with middle crustal rocks during the extrusion of the orogenic root of the Variscan chain. We propose that a system of high‐temperature, orogen‐parallel shear zones that developed under a transpressive dextral tectonic regime caused the exhumation of the entire sequence. This tectonic complex is thus made up of rocks having undergone different P–T conditions (eclogite‐?, high‐pressure granulite facies and amphibolite facies) at different times, reflecting the progressive foreland migration of the orogenic front. The Solenzara granulites were derived from burial of continental crust to high‐pressure (1.8–1.4 GPa) and high‐ to ultrahigh‐temperature conditions (900–1000 °C) during the Variscan convergence: U–Pb ELA‐ICPMS zircon dating constrained the timing of this metamorphism at c. 360 Ma. The gneisses cropping out at Porto Vecchio are middle crustal‐level rocks that reached their peak temperature conditions (700–750 °C at <1.0 GPa) at c. 340 Ma. The diachronism of the metamorphic events, the foliation patterns and their geometry suggest that the granulites were exhumed to middle crustal levels through channel flow tectonics under continuous compression. The amphibolite facies gneisses of Porto Vecchio and the granulites of Solenzara were accreted through the development of a major dextral mylonitic zone forming under amphibolite facies conditions: in situ monazite isotope dating (ELA‐ICPMS) revealed that this deformation occurred at c. 320 Ma and was accompanied by the emplacement of syntectonic high‐K melts. A final HTLP static overprint, constrained at 312–308 Ma by monazite U‐Th‐Pb isotope dating, is related to the emplacement of the igneous products of the Sardinia‐Corsica batholith and marks the transition from the Variscan orogenic event to the Permian extension.