The triple isotopic composition of oxygen in leaf water

The isotopic composition of atmospheric O₂ depends on the rates of oxygen cycling in photosynthesis, respiration, photochemical reactions in the stratosphere and on δ¹⁷O and δ¹⁸O of ocean and leaf water. While most of the factors affecting δ¹⁷O and δ¹⁸O of air O₂ have been studied extensively in recent years, δ¹⁷O of leaf water—the substrate for all terrestrial photosynthesis—remained unknown. In order to understand the isotopic composition of atmospheric O₂ at present and in fossil air in ice cores, we studied leaf water in field experiments in Israel and in a European survey. We measured the difference in δ¹⁷O and δ¹⁸O between stem and leaf water, which is the result of isotope enrichment during transpiration. We calculated the slopes of the lines linking the isotopic compositions of stem and leaf water. The obtained slopes in ln(δ¹⁷O + 1) vs. ln(δ¹⁸O + 1) plots are characterized by very high precision (∼0.001) despite of relatively large differences between duplicates in both δ¹⁷O and δ¹⁸O (0.02-0.05‰). This is so because the errors in δ¹⁸O and δ¹⁷O are mass-dependent. The slope of the leaf transpiration process varied between 0.5111 ± 0.0013 and 0.5204 ± 0.0005, which is considerably smaller than the slope linking liquid water and vapor at equilibrium (0.529). We further found that the slope of the transpiration process decreases with atmospheric relative humidity (h) as 0.522-0.008 × h, for h in the range 0.3-1. This slope is neither influenced by the plant species, nor by the environmental conditions where plants grow nor does it show strong variations along long leaves.     

Orbital cyclicity in sedimentary sequence and climatic indications of C-O isotopes from Lower Cretaceous in Qingxi Sag,Jiuquan Basin,NW China

Sedimentary deposits of the Lower Cretaceous Xiagou Formation form the most significant potential hydrocarbon reservoirs in the Qingxi Sag, Jiuquan Basin(NW China). Zircon U-Pb ages of the dated basalts at the top of the Xiagou Formation give an isochron age of 115.6 Ma, and the sedimentation interval of the Xiagou Formation was speculated to range from about 125/124 Ma to 115 Ma based on paleontological research and stratigraphic correlation analysis. Here we use GR logging data as a palaeoenvironmental and palaeoclimatic proxy to conduct a detailed cyclostratigraphic study of five selected wells. Power spectra, evolutionary fast Fourier transformation and wavelet analysis all reveal significant sedimentary cycles in the Xiagou Formation. The ratios of cycle wavelengths in these stratigraphic units are 33.82 m : 7.91 m : 3.06 m : 1.79 m, which is similar to the ratio of orbital targets of 20 : 5 : 2 : 1. The ratio of 20 : 5 : 2 : 1 is interpreted as Milankovitch cycles of 405 kyr long eccentricity,100 kyr short eccentricity, 37 kyr obliquity, and 22 kyr precession cycles respectively. A high-resolution astronomical time scale is constructed by tuning the stratigraphy into target curves of orbital cycles respectively. Based on the astronomical time scale, the absolute ages of 55 samples were estimated,which are used for subsequent stable carbon and oxygen isotope stratigraphy analysis. The analysis results of the five studied wells in the Qingxi Sag indicate:(1) a negative trend of δ~(13)C values upwards in the Xiagou Formation, and(2) negative δ~(18)O values with a positive trend upwards. Both relatively heavy values and pronounced covariances of δ~(13)C values and δ~(18)O values indicate an arid-evaporationcontrolled climate during the sedimentary period of the Lower Cretaceous Xiagou Formation, Qingxi Sag, Jiuquan Basin. Moreover, positive covariances of SQK_1g_(2+3) indicate extremely high temperature, and negative covariances of SQK_1g_1 indicate a relatively low temperature.     

The West European stress field: new data and interpretation

The mapped stress field of Western Europe reflects the tectonic process active there. A traverse of stress measurements from the Alps and through their northern foreland to the southern border of the Lower Rhine Embayment identifies three distinct stress sub-provinces; the Western Alps, the blocks on both flanks of the Rhinegraben, and the Rhenish Shield. The Alps have high magnitude stresses up to 35 MPa in the direction of maximum compression, here called δ_1h. The general direction of δ_1h is about 140°. The foreland has the same directional trend of δ_1h with a magnitude reduced to about 2.0 MPa. Local anomalies in magnitude and direction occur along the course of the Rhinegraben which is a site of active sinistral shear. The Rhenish Shield shows an internal zonation of the stress field. The magnitudes of the stresses are low (usually negative) along the axis connecting the northern end of the Rhinegraben with the rifting of the Lower Rhine Embayment. The direction there is about 150°. On the eastern and western flanks of the shield the stress directions are essentially the same as in the southern blocks. These zones are distant from the belt of active strain release, consequently stresses of up to 4.0 MPa have accumulated.     

Hydro-geochemical and isotopic fluid evolution of the Los Azufres geothermal field,Central Mexico

Hydrothermal alteration at Los Azufres geothermal field is mostly propylitic with a progressive dehydration with depth and temperature increase. Argillic and advanced argillic zones overlie the propylitic zone owing to the activity of gases in the system. The deepest fluid inclusions (proto-fluid) are liquid-rich with low salinity, with NaCl dominant fluid type and ice melting temperatures (T_mi) near zero (0 °C), and salinities of 0.8 wt% NaCl equivalent. The homogenization temperature (T_h)  = 325 ± 5 °C. The boiling zone shows T_h = ±300 °C and apparent salinities between 1 and 4.9 wt% NaCl equivalent, implying a vaporization process and a very important participation of non-condensable gases (NCGs), mostly CO₂. Positive clathrate melting temperatures (fusion) with T_h = 150 °C are observed in the upper part of the geothermal reservoir (from 0 to 700 m depth). These could well be the evidence of a high gas concentration. The current water produced at the geothermal wells is NaCl rich (geothermal brine) and is fully equilibrated with the host rock at temperatures between T = 300 and 340 °C. The hot spring waters are acid-sulfate, indicating that they are derived from meteoric water heated by geothermal steam. The NCGs related to the steam dominant zone are composed mostly of CO₂ (80–98% of all the gases). The gases represent between 2 and 9 wt% of the total mass of the fluid of the reservoir.The authors interpret the evolution of this system as deep liquid water boiling when ascending through fractures connected to the surface. Boiling is caused by a drop of pressure, which favors an increase in the steam phase within the brine ascending towards the surface. During this ascent, the fluid becomes steam-dominant in the shallowest zone, and mixes with meteoric water in perched aquifers. Stable isotope compositions (δ¹⁸O–δD) of the geothermal brine indicate mixing between meteoric water and a minor magmatic component. The enrichment in δ¹⁸O is due to the rock–water interaction at relatively high temperatures. δ¹³C stable isotope data show a magmatic source with a minor meteoric contribution for CO₂. The initial isotopic value δ³⁴S_RES = −2.3‰, which implies a magmatic source. More negative values are observed for shallow pyrite and range from δ³⁴S (FeS₂) = −4‰ to −4.9‰, indicating boiling. The same fractionation tendencies are observed for fluids in the reservoir from results for δ¹⁸O.     

Thermal history of the unsaturated zone at Yucca Mountain,Nevada, USA

Secondary calcite, silica and minor amounts of fluorite deposited in fractures and cavities record the chemistry, temperatures, and timing of past fluid movement in the unsaturated zone at Yucca Mountain, Nevada, the proposed site of a high-level radioactive waste repository. The distribution and geochemistry of these deposits are consistent with low-temperature precipitation from meteoric waters that infiltrated at the surface and percolated down through the unsaturated zone. However, the discovery of fluid inclusions in calcite with homogenization temperatures (T_h) up to ∼80 °C was construed by some scientists as strong evidence for hydrothermal deposition. This paper reports the results of investigations to test the hypothesis of hydrothermal deposition and to determine the temperature and timing of secondary mineral deposition. Mineral precipitation temperatures in the unsaturated zone are estimated from calcite- and fluorite-hosted fluid inclusions and calcite δ¹⁸O values, and depositional timing is constrained by the ²⁰⁷Pb/²³⁵U ages of chalcedony or opal in the deposits. Fluid inclusion T_h from 50 samples of calcite and four samples of fluorite range from ∼35 to ∼90 °C. Calcite δ¹⁸O values range from ∼0 to ∼22‰ (SMOW) but most fall between 12 and 20‰. The highest T_h and the lowest δ¹⁸O values are found in the older calcite. Calcite T_h and δ¹⁸O values indicate that most calcite precipitated from water with δ¹⁸O values between −13 and −7‰, similar to modern meteoric waters.     

Geochemistry,geochronology and Hf isotope of granitoids in the Chinese Altai: Implications for Paleozoic tectonic evolution of the Central Asian Orogenic Belt

The Chinese Altai in northwestern Xinjiang has numerous outcrops of granitoids which provide critical information on accretionary orogenic processes and crustal growth of the Central Asian Orogenic Belt.Zircon U-Pb ages, Hf-isotopic compositions and whole-rock geochemistry of monzogranite and granodiorites in the Qinghe County are employed to elucidate Paleozoic tectonics of the Chinese Altai. Granodiorites have crystallization ages of 424.6 ± 3.1 Ma(MSWD = 0.23) and 404.0 ± 3.4 Ma(MSWD = 0.18);monzogranite was emplaced in the early Permian with a crystallization age of 293.7 ± 4.6 Ma(MSWD = 1.06). Both granodiorites and monzogranite are I-type granites with A/CNK ratios of 0.92 -0.97 and 1.03 -1.06, respectively. They also show similar geochemical features of high HREE and Y contents, low Sr contents and Sr/Y ratios, as well as enrichment of Cs, Rb, Th and U, and depletion of Nb, Ta, P and Ti.These geochemical features indicate that the monzogranite and granodiorites were formed in an arc setting related to subduction. The gneissic monzogranites display high SiO_2 and K_2 O contents, and belong to the high-K calc-alkaline series. In the chondrite normalized REE distribution pattern, the monzogranite samples exhibit enrichment of LREE with strong negative Eu anomalies(σE u =0.44 -0.53), zircon εHf(t) values from +7.24 to +12.63 and two-stage Hf model ages of 463 -740 Ma. This suggests that the monzogranite was generated from the mixing of pelitic and mantle material. The granodiorite samples are calc-alkaline granites with lower contents of Si O_2 and Na_2 O + K_2 O, higher contents of TiO_2, Fe_2O_3~t, MgO and CaO compared to the monzogranite samples. They also show enrichment of LREE and moderate negative Eu anomalies(σE u= 0.54 =0.81), as well as slightly higher differentiation of LREE than that of HREE. The425 Ma granodiorite has zircon εHf(t) values from -0.51 to +1.98 and two-stage Hf model ages of 1133 -1240 Ma, whereas the 404 Ma granodiorite displays those of +2.52 to +7.50 and 816 -1071 Ma.Geochemistry and zircon Hf isotopic compositions indicate that granodiorites were formed by partial melting of juvenile lower crust. Together with regional geology and previous data, the geochemical and geochronological data of the monzogranite and granodiorites from this study suggest long-lived subduction and accretion along the Altai Orogen during ca. 425 -294 Ma.     

Depositional age and tectonic environment of the Gouap banded iron formations from the Nyong group,SW Cameroon:Insights from isotopic,geochemical and geochronological studies of drillcore samples

The discovery of the Gouap banded iron formations(BIFs)-hosted iron mineralization in the northwestern of the Nyong Group(Ntem Complex)in southwestern Cameroon provides unique insights into the geology of this region.In this contribution,we firstly report detailed study of geochemistry,isotopic and geochronology of well preserved samples of the Gouap BIFs collected from diamond drillcores.The Gouap BIFs consist mainly of amphibole BIFs and amphibole-pyrite BIFs characterized by dominant Fe₂O₃+SiO₂contents and variable contents of CaO,MgO and SO₃,consistent with the presence of amphibole,chlorite,epidote and pyrite,formed during amphibolite facies metamorphism and overprinted hydrothermal event.The amphibole–pyrite BIFs are typically enriched in trace and rare earth elements(REE)compared to the amphibole BIFs,suggesting the influence of detrital materials as well as secondary hydrothermal alteration.The Post Archean Australian Shale(PAAS)-normalized REE–Y profiles of the Gouap BIFs display positive La,Eu anomalies,weak negative Ce anomalies,indicating a mixture of low-temperature hydrothermal fluids and relatively oxic conditions probably under relative shallow seawater.We present here the first isotopic data of BIFs within the Ntem Complex.Theδ³⁰Si_NBS28values of the quartz from the Gouap BIFs vary from-1.5‰to-0.3‰and from-0.8‰to-0.9‰for the amphibole BIFs and amphibole–pyrite BIFs,respectively.The quartz hasδ¹⁸OV-SMOW values of 6.8‰–9.5‰(amphibole BIFs)and 9.2‰–10.6‰(amphibole–pyrite BIFs).The magnetite from the Gouap BIFs showsδ¹⁸O values ranging from-3.5‰to-1.8‰and from-3‰to-1.7‰for the amphibole BIFs and amphibole–pyrite BIFs,respectively.Moreover,the pyrite grains in the amphibole–pyrite BIFs displayδ34S values of 1.1‰–1.8‰.All isotopic data of the Gouap BIFs confirm that they might have precipitated from low-temperature hydrothermal fluids with detrital input distant from the volcanic activity.According to their geochemical and isotopic characteristics,we propose that the Gouap BIFs belong to the Superior type.In situ U–Pb zircon dating of BIFs was conducted to assess the BIF depositional age based on strong evidence of zircon in thin section.The Gouap BIFs were probably deposited at 2422±50 Ma in a region where sediments extended from continental shelf to deep-water environments along craton margins like the Caue Formation of the Minas Supergroup,Brazil.The studied BIFs have experienced regional hydrothermal activity and metamorphism at 2089±8.3 Ma during the Eburnean–Transamazonian orogeny.These findings suggest a physical continuity between the protocratonic masses of both Sao Francisco and Congo continents in the Rhyacian Period.     

Intermediate sulfidation epithermal gold-base metal deposits in Tertiary subaerial volcanic rocks,Sahinli/Tespih Dere (Lapseki/Western Turkey)

Gold in the Sahinli and Tespih Dere intermediate sulfidation gold-base metal deposits in Western Turkey occurs in relatively deep epithermal quartz veins along with base metal minerals which have epithermal textures, including plumose quartz, vug infills, comb and cockade textures and matrix-supported milled breccias. The total sulfide content of the veins in the area is variable ranging from < 1% to 60% and is dominated by pyrite, galena, sphalerite and chalcopyrite. Sphalerite is Fe-poor (0.6 to 1.4 mol% FeS). Minor amounts of Ag-rich tetrahedrite are present. Primary hydrothermal alteration minerals include illite/muscovite, mixed-layer illite/smectite (11.6 Å) and clinochlore towards the east and, alunite, dickite/nacrite and pyrophyllite towards the west at Sahinli; major illite/muscovite and dickite occur at Tespih Dere and Sarioluk, respectively.Fluid inclusions in main-stage quartz at Sahinli are only liquid-rich, with homogenization temperatures ranging from 220 to 322 °C and the majority of T_h values between 250 and 300 °C. Salinity ranges from 4.3 to 6.9 wt.% NaCl equiv. First ice-melting temperatures (T_mf) between ?24.5 and ?19.0 °C indicate that the fluids were dominated by NaCl – H₂O during mineralization. The relatively higher average T_h at the Tespih Dere deposit (295 °C) is attributed to a relatively deeper level of exposure.Calculated δ¹⁸O values indicate that ore-forming hydrothermal fluids in the study area had δ¹⁸O_H2O ranging from + 1.1 to + 9.7‰ (average = 3.8‰), strongly ¹⁸O-enriched compared with present-day hydrothermal meteoric water in the area (δ¹⁸O = ?8.5‰). δD values of fluid inclusions in quartz range from ?58 to ?93‰ and δD values of clay minerals and alunite from ?40 to ?119‰. δD values from intermediate argillic alteration (average = ?68‰) in the study area are very similar to δD values of the present-day local geothermal system (average δD = ?54‰) whereas δD values from advanced-argillic alteration (average δD = ?33‰) are very different from the present-day local geothermal system.The δ³⁴S values in samples from the Sahinli and Tespih Dere deposits average ?2.9‰ for pyrite; ?3.3‰ for chalcopyrite; ?5.4‰ for sphalerite and ?7.6‰ for galena. These data are consistent with derivation of the sulfur from either igneous rocks or possibly from local wallrock.     

Assimilation of carbonate country rock by the parent magma of the Panzhihua Fe-Ti-V deposit（SW China）：Evidence from stable isotopes

The Panzhihua intrusion in southwest China is part of the Emeishan Large Igneous Province and host of a large Fe-Ti-V ore deposit.During emplacement of the main intrusion,multiple generations of mafic dykes invaded carbonate wall rocks,producing a large contact aureole.We measured the oxygen-isotope composition of the intrusions,their constituent minerals,and samples of the country rock.Magnetite and plagioclase from Panzhihua intrusion haveδ¹⁸O values that are consistent with magmatic equilibrium, and formed from magmas withδ¹⁸O values that were 1-2‰higher than expected in a mantle-derived magma.The unmetamorphosed country rock has highδ¹⁸O values,ranging from 13.2‰（sandstone） to 24.6-28.6‰（dolomite）.The skarns and marbles from the aureole have lowerδ¹⁸O andδ¹³C values than their protolith suggesting interaction with fluids that were in exchange equilibrium with the adjacent mafic magmas and especially the numerous mafic dykes that intruded the aureole.This would explain the alteration ofδ¹⁸O of the dykes which have significantly higher values than expected for a mantle-derived magma.Depending on the exactδ¹⁸O values assumed for the magma and contaminant, the amount of assimilation required to produce the elevatedδ¹⁸O value of the Panzhihua intrusion was between 8 and 13.7 wt.%,assuming simple mixing.The exact mechanism of contamination is unclear but may involve a combination of assimilation of bulk country rock,mixing with a melt of the country rock and exchange with CO₂-rich fluid derived from decarbonation of the marls and dolomites.These mechanisms,particularly the latter,were probably involved in the formation of the Fe-Ti-V ores.     

Influencing factors and significance of organic and inorganic nitrogen isotopic compositions in lacustrine sedimentary rocks

Comprehensive nitrogen biogeochemical cycle has been reconstructed for representative lacustrine organic-rich sedimentary rock in China, namely the Triassic Yanchang Formation (YF, 199–230 Ma) in Ordos and the Cretaceous Qingshankou Formation (QF, 86–92 Ma) in Songliao basins, by evaluating the organic and inorganic nitrogen isotopic compositions rather than only organic or bulk nitrogen isotopic compositions. The results indicate that the nitrogen isotope values of bulk rock (δ¹⁵N_bulk) in the non-metamorphic stage are significantly different from that of kerogen, which challenge the conceptual framework of sedimentary nitrogen isotope interpretation. The δ¹⁵N_bulk from the YF and QF were lower than their respective the nitrogen isotope values of kerogen (δ¹⁵N_ker), with offsets up to ～5.1‰, which have the inverse relationship for the metamorphosed rock. Thermal evolution did not significantly modify the δ¹⁵N of bulk rock and kerogen. The δ¹⁵N of sediments from the YF (δ¹⁵N_bulk, 1.6‰–5.6‰) were lower than that of rock from the QF (δ¹⁵N_bulk, 10.2‰–15.3‰). The nitrogen isotope values of silicate incorporated nitrogen (δ¹⁵N_sil) were slightly lower than those of the δ¹⁵N_ker in the YF and obviously lower for the QF. The fact that different nitrogen cycles occur in the YF and QF due to the different depositional redox conditions leads to different isotopic results. The YF water environment dominated by oxic conditions is not conducive to the occurrence of denitrification and anammox, and no abundant N₂ loss leads to the relatively light δ¹⁵N_bulk. In the stratified water for the QF, redox transition zone promotes denitrification and anammox, resulting in the heavy δ¹⁵N_bulk of rock and promotes the DNRA, resulting in heavy δ¹⁵N_ker and low δ¹⁵N_sil.     

Effects of clay minerals and biosurfactants on isotopic and molecular characteristics of methane encaged in pressure vessel gas hydrates

The stable isotope values of carbon (δ¹³C_methane) and hydrogen (δ²H_methane) from methane molecules trapped in gas hydrates are useful for differentiation of methane from microbial and thermal origins, providing valuable information during hydrocarbon exploration. Recent studies have reported catalysis of methane hydrates when smectite clays and biosurfactants are present in hydrate-hosting sediments, but catalytic influences on the values of δ¹³C_methane and δ²H_methane are not well documented. In this study, pressure vessel methane hydrates were formed from solutions in contact with smectite clays (montmorillonite and nontronite) and biosurfactants (rhamnolipids and surfactin). Experiments show less than 1‰ differences in values of δ¹³C_methane between free and encaged molecules and up to 10‰ variations in values of δ²H_methane between free and encaged molecules. Notably, methane consumption increased in methane hydrates formed from solutions containing biosurfactants and biosurfactant–smectite mixtures. Results presented here indicate that a hydrate formed in the presence of smectite clays and biosurfactants are characterized by small shifts in free and encaged values of δ¹³C_methane and δ²H_methane and do not complicate interpretation of gas origin. In contrast, methane consumption in hydrates formed under the catalytic effect of smectite clays and biosurfactants modifies gas wetness, obscures gas origin and complicates interpretation of thermal maturity.     

Dielectric constants of apatite,epidote, vesuvianite,and zoisite,and the oxide additivity rule

The dielectric constants and dielectric loss values of 4 Ca-containing minerals were determined at 1 MHz using a two-terminal method and empirically determined edge corrections. The results are: vesuvianitel κ′ _a=9.93 tan δ=0.006 κ′ _c=9.79 tan δ=0.005 vesuvianitel κ′ _a=10.02 tan δ=0.002 κ′ _c=9.85 tan δ=0.003 zoisite1 κ′ _a =10.49 tan δ=0.0006 κ′ _b =15.31 tan δ=0.0008 κ′ _c=9.51 tan δ=0.0008 zoisite2 κ′ _a =10.55 tan δ=0.0011 κ′ _b =15.45 tan δ=0.0013 κ′ _c=9.39 tan δ=0.0008 epidote κ′ ₁₁= 9.52 tan δ=0.0008 κ′ ₂₂=17.1 tan δ=0.0009 κ′ ₃₃= 9.37 tan δ=0.0006 fluorapatite1 κ′ _a =10.48 tan δ=0.0008 κ′ _c = 8.72 tan δ=0.0114 fluorapatite2 κ′ _a =10.40 tan δ=0.0010 κ′ _c=8.26 tan δ=0.0178 The deviation (δ) between measured dielectric polarizabilities as determined from the Clausius-Mosotti equation and those calculated from the sum of oxide polarizabilities according to α _D (mineral)=∑ α _D (oxides) for vesuvianite is ～ 0.5%. The large deviations of epidote and zoisite from the additivity rule with Δ=+ 10.1 and + 11.7%, respectively, are attributed to “rattling” Ca ions. The combined effects of both a large F thermal parameter and possible F-ion conductivity in fluorapatite are believed to be responsible for Δ=+2–3%. Although variation of oxygen polarizability with oxygen molar volume (V_o) is believed to affect the total polarizabilities, the variation of V_o in these Ca minerals is too small to observe the effect.     

Predicting standard penetration test N-value from cone penetration test data using artificial neural networks

Standard Penetration Test(SPT) and Cone Penetration Test(CPT) are the most frequently used field tests to estimate soil parameters for geotechnical analysis and design.Numerous soil parameters are related to the SPT N-value.In contrast,CPT is becoming more popular for site investigation and geotechnical design.Correlation of CPT data with SPT N-value is very beneficial since most of the field parameters are related to SPT N-values.A back-propagation artificial neural network(ANN) model was developed to predict the N6o-value from CPT data.Data used in this study consisted of 109 CPT-SPT pairs for sand,sandy silt,and silty sand soils.The ANN model input variables are:CPT tip resistance(q_c),effective vertical stress(σ'_v),and CPT sleeve friction(f_s).A different set of SPT-CPT data was used to check the reliability of the developed ANN model.It was shown that ANN model either under-predicted the N_(60)-value by 7-16%or over-predicted it by 7-20%.It is concluded that back-propagation neural networks is a good tool to predict N_(60)-value from CPT data with acceptable accuracy.     

Effect of plant life form on relationship between δD values of leaf wax n-alkanes and altitude along Mount Taibai, China

We present δD_wax values from different forms of plants and soils, and δD_sw values from soil water along the northern slope of Mount Taibai, China. The results show a highly negative linear correlation of the δD_wax values for soils with altitude (R² 0.74) and we observed the same correlation for δD_sw values of soil water with altitude (R² 0.68). The δD_wax of living plants behaves like the soil, but does not exhibit a significant linear correlation with altitude (R² 0.11). The δD_wax values of woody plants and grasses also show a similar trend with respect to altitude with significant and no linear correlation, respectively (R² 0.50 for woody plants and 0.17 for grass), which suggest that the “altitude effect” can not be well documented for the δD_wax values of living plants, which may be due to differences in plant type and/or evapotranspiration controlled by the plant microclimate. The ε_wax-sw values of woody plants, grasses and soil show minor fluctuations with altitude. However, the ε_wax-sw and δD_wax values of woody plants are roughly 51‰ and 50‰ more positive, respectively, than those of grasses, suggesting that an “altitude effect” could be documented in the δD_wax of woody plants and grasses, with each responding independently to changes in precipitation along the altitude transect. Additionally, the ε_wax-sw values of soil are relatively constant with altitude, suggesting that the altitudinal change in the proportions between woody plant and grass input to soils will likely change the relationship between the δD_wax values of soil n-alkanes and altitude.     

Calcification rate and the stable carbon, oxygen, and nitrogen isotopes in the skeleton, host tissue, and zooxanthellae of bleached and recovering Hawaiian corals

We tested the effectiveness of stable isotopes as recorders of physiological changes that occur during coral bleaching and recovery. Montipora capitata and Porites compressa fragments were bleached in outdoor tanks with seawater temperature raised to 30 °C (treatment corals) for one month. Additional fragments were maintained at 27 °C in separate tanks (control corals). After one month, (0 months recovery), buoyant weight was measured and a subset of fragments was frozen. Remaining fragments were returned to the reef for recovery. After 1.5, 4, and 8 months, fragments were collected, measured for buoyant weight, and frozen. Fragments were analyzed for stable carbon and oxygen isotopic compositions of the skeleton (δ¹³C_s; δ¹⁸O_s) and nitrogen and carbon isotopic compositions of the host tissue (δ¹⁵N_h; δ¹³C_h) and zooxanthellae (δ¹⁵N_z; δ¹³C_z). δ¹³C_s decreased immediately after bleaching in M. capitata, but not in P. compressa. δ¹⁸O_s of both species failed to record the warming event. During the remaining months of recovery, δ¹³C_s and δ¹⁸O_s were more enriched in treatment than control corals due to decreases in calcification and metabolic fractionation during that time. Increased δ¹⁵N_h of treatment P. compressa may be due to expelled zooxanthellae during bleaching and recovery. Increased δ¹⁵N_z at 1.5 months in treatment fragments of both species reflects the increased incorporation of dissolved inorganic nitrogen to facilitate mitotic cell division and/or chl a/cell recovery. Changes in δ¹³C_h and δ¹³C_z at 1.5 months in treatment M. capitata indicated a large increase in heterotrophically acquired carbon relative to photosynthetically fixed carbon. We experimentally show that isotopes in coral skeleton, host tissue and zooxanthellae can be used to verify physiological changes during bleaching and recovery, but their use as a proxy for past bleaching events in the skeletal record is limited.     

Geochemical evolution of the Mangalwar Complex,Aravalli Craton,NW India:Insights from elemental and Nd-isotope geochemistry of the basement gneisses

The Banded Gneissic Complex(BGC) of the Aravalli Craton is divided into BGC-I and BGC-Ⅱ; the BGC-Ⅱ(central Rajasthan) is comprised of the Sandmata Complex and the Mangalwar Complex. We report elemental and Nd-isotope geochemistry of basement gneisses of the Mangalwar Complex and constrain its origin and evolution. Geochemically, the basement gneisses have been classified as low-SiO_2 gneisses(LSG) and high-SiO_2 gneisses(HSG). Both the LSG and HSG are potassic, calc-alkaline and peraluminous in nature. The LSG are enriched in incompatible(K, Sr, Ba, large ion lithophile elements) and compatible elements(MgO, Cr, and Ni). They display fractionated rare earth element patterns(avg.La_N/Yb_N=12.1)with small Eu-anomaly(δEu=0.9), and exhibit negative anomalies of Nb and Ti in primitive mantlenormalized multi-element diagram. In terms of Nd-isotope geochemistry, the LSG are characterized by_(εNd)(t)=4.2 and depleted mantle model age of 3.3 Ga. To account for these geochemical characteristics we propose a three-stage petrogenetic model for the LSG:(1) fluids released from dehydration of subducting slab metasomatised the mantle-wedge;(2) the subducting slab underwent slab-breakoff causing upwelling and decompression melting of the asthenosphere during waning stage of subduction; and(3)upwelling asthenosphere provided the requisite heat for partial melting of the metasomatised mantlewedge leading to generation of the LSG parental magma. Asthenospheric upwelling also contributed in the LSG petrogenesis which is evident from its high Mg#(avg. 0.53). The LSG formed in this way are contemporary and chemically akin to sanukitoids of the BGC-I and Archean sanukitoids reported elsewhere. This provides a basis to consider the LSG as a part of the BGC-I. Contrary to the LSG, the HSG are depleted in compatible elements(MgO=avg. 1.1 wt.%; Cr=avg. 8 ppm; Ni=avg. 6 ppm) but enriched in incompatible elements(Sr=avg. 239 ppm, Ba=avg. 469 ppm). Its_(εNd)(t) values vary from-9.5 to-5.4.These chemical features of the HSG are akin to potassic granitoids found elsewhere. In this backdrop, we propose that the HSG suite of the Mangalwar Complex was derived from re-melting(partial) of an older crust(TTG?) occurring within the BGC-Ⅱ.     

Chemical,isotopic and amino acid composition of Mukundpura CM2.0(CM1) chondrite: Evidence of parent body aqueous alteration

The carbonaceous chondrites are intriguing and unique in the sense that they are the only rocks that provide pristine records of the early solar nebular processes. We report here results of a detailed mineralogical, chemical, amino acid and isotopic studies of a recently observed fall at Mukundpura, near Jaipur in Rajasthan, India. Abundance of olivines in this meteorite is low and of serpentine minerals is high. FeO/SiO_2 = 1.05 in its Poorly Characterized Phases(PCP) is similar to that observed in other CM2.0 chondrites. The water content of ～9.8 wt.% is similar to that found in many other CM chondrites.Microscopic examination of matrix shows that its terrestrial weathering grade is WO but aqueous parent body alteration is high, as reflected in low abundance of identifiable chondrules and abundant remnants of chondrules(～7%). Thus, most of the chondrules formed initially have been significantly altered or dissolved by aqueous alterations on their parent bodies. The measured bulk carbon(2.3%) and nitrogen content and their isotopic(δ¹³C =-5.5‰, δ¹⁵N = 23.6%0) composition is consistent with CM2.0 classification probably bordering CM1. Several amino acids such as Alanine, Serine, Proline, Valine, Threonine,Leucine, Isoleucine, Asparagine and Histamine are present. Tyrosine and Tryptophan may occur in trace amounts which could not be precisely determined. All these data show that Mukundpura chondrite lies at the boundary of CM2.0 and CM1 type carbonaceous chondrites making it one of the most primitive chondrites.     

Petrology,geochemistry and geochronology of the Zhongcang ophiolite,northern Tibet: implications for the evolution of the Bangong-Nujiang Ocean

Ophiolites are widespread along the Bangong-Nujiang suture zone, northern Tibet. However, it is still debated on the formation ages and tectonic evolution process of these ophiolites. The Zhongcang ophiolite is a typical ophiolite in the western part of the Bangong-Nujiang suture zone. It is composed of serpentinized peridotite, cumulate and isotropic gabbros, massive and pillow basalts, basaltic volcanic breccia, and minor red chert. Zircon SHRIMP Ue Pb dating for the isotropic gabbro yielded weighted mean age of 163.4 ± 1.8 Ma. Positive zircon ε Hf(t) values(+15.0 to +20.2) and mantle-like σ~(18)O values(5.29 ±0.21)% indicate that the isotropic gabbros were derived from a long-term depleted mantle source. The isotropic gabbros have normal mid-ocean ridge basalt(N-MORB) like immobile element patterns with high Mg O, low TiO_2 and moderate rare earth element(REE) abundances, and negative Nb,Ti, Zr and Hf anomalies. Basalts show typical oceanic island basalt(OIB) geochemical features, and they are similar to those of OIB-type rocks of the Early Cretaceous Zhongcang oceanic plateau within the Bangong-Nujiang Ocean. Together with these data, we suggest that the Zhongcang ophiolite was probably formed by the subduction of the Bangong-Nujiang Ocean during the Middle Jurassic. The subduction of the Bangong-Nujiang Tethyan Ocean could begin in the Earlye Middle Jurassic and continue to the Early Cretaceous, and finally continental collision between the Lhasa and Qiangtang terranes at the west Bangong-Nujiang suture zone probably has taken place later than the Early Cretaceous(ca. 110 Ma).     

Microvariability of line profiles in the spectra of OB stars: δOri A

We have studied variability of the spectral lines of the OB star δOri A—the brightest component of the δOri triple system. Forty spectra with signal-to-noise ratios ≈500–800 and a time resolution of four minutes were obtained. We detected variability in the HeIIλ4686, HeIλ4713, and Hβ absorption and the CIIIλ5696 emission profiles. The amplitude of the variability is ≈(0.5–1)% of the continuum intensity. The dynamical wavelet spectrum of the profile variations reveals large-scale components in the interval 25–50 km/s that move within the-V sin i to V sin i band for the primary star of the system, Aa¹, with a band crossing time of 4^h–5^h. However, some of the variable features go outside the band, presumably due to either imhomogeneities in the stellar wind from δOri Aa¹ or nonradial pulsations of the weaker components of the system, Aa² or Ab. The detected variability may be cyclic with a period of ≈4^h. We suggest that it is associated with nonradial pulsations of the primary in the sector mode (l,m) = (2, ?2).     

The origins and behaviour of carbon in a major semi-arid river,the Murray River,Australia, as constrained by carbon isotopes and hydrochemistry

δ¹³C values of dissolved inorganic C (DIC), dissolved organic C (DOC), and particulate organic C (POC) together with δ¹⁸O and δ²H values of water, δ³⁴S values of dissolved SO₄, and major ion concentrations were measured in the Murray River and its tributaries between November 2005 and April 2007 to constrain the origins and behaviour of riverine C. δ¹³C_DIC values in the Murray River vary between −9.5 and −4.7‰ with a range of <3‰ within any sampling round. δ¹³C_DIC values of the tributaries are −11.0‰ to −5.1‰. DIC concentrations of the Murray River increase from ∼25 mg/L in the middle and upper reaches of the river to 45–55 mg/L in the lower reaches. However, the mass ratio of DIC as a proportion of the total dissolved solids (TDS) decreases from ∼0.6–0.7 in the headwaters to ∼0.2–0.3 in the lower reaches of the river, with similar downstream changes in DIC/Cl ratios. This precludes simple evaporative concentration of DIC and is interpreted as the river evading CO₂; this interpretation is consistent with pCO₂ values that are in the range 550–11,200 ppm volume (ppmv), which are far higher than those in equilibrium with the atmosphere (∼360 ppmv). The δ¹³C_DIC values are similar to those that would be produced by the weathering of marine limestone (δ¹³C ∼ 0‰). However, the lack of marine limestones cropping out in the Murray–Darling Basin and the relatively uniform δ¹³C_DIC values of the Murray River (even in upland reaches where the dominant rock types are metamorphosed silicates and granites) make this unlikely. Rather the high pCO₂ values and δ¹³C_DIC values are best explained by a combination of mineralisation of low δ¹³C organic C and evasion to the atmosphere. The rate of these two processes may attain near steady state and control both DIC concentrations and δ¹³C values.