Rates of rockwall slope erosion in the upper Bhagirathi catchment,Garhwal Himalaya

Rockwall slope erosion is defined for the upper Bhagirathi catchment using cosmogenic Beryllium-10 (¹⁰Be) concentrations in sediment from medial moraines on Gangotri glacier. Beryllium-10 concentrations range from 1.1 ± 0.2 to 2.7 ± 0.3 × 10⁴ at/g SiO₂, yielding rockwall slope erosion rates from 2.4 ± 0.4 to 6.9 ± 1.9 mm/a. Slope erosion rates are likely to have varied over space and time and responded to shifts in climate, geomorphic and/or tectonic regime throughout the late Quaternary. Geomorphic and sedimentological analyses confirm that the moraines are predominately composed of rockfall and avalanche debris mobilized from steep relief rockwall slopes via periglacial weathering processes. The glacial rockwall slope erosion affects sediment flux and storage of snow and ice at the catchment head on diurnal to millennial timescales, and more broadly influences catchment configuration and relief, glacier dynamics and microclimates. The slope erosion rates exceed the averaged catchment-wide and exhumation rates of Bhagirathi and the Garhwal region on geomorphic timescales (10³−10⁵ years), supporting the view that erosion at the headwaters can outpace the wider catchment. The ¹⁰Be concentrations of medial moraine sediment for the upper Bhagirathi catchment and the catchments of Chhota Shigri in Lahul, northern India and Baltoro glacier in Central Karakoram, Pakistan show a tentative relationship between ¹⁰Be concentration and precipitation. As such there is more rapid glacial rockwall slope erosion in the monsoon-influenced Lesser and Greater Himalaya compared to the semi-arid interior of the orogen. Rockwall slope erosion in the three study areas, and more broadly across the northwest Himalaya is likely governed by individual catchment dynamics that vary across space and time. © 2019 The Authors. Earth Surface Processes and Landforms Published by John Wiley & Sons, Ltd.     

Mineralogy, geochemistry, and Nd isotope composition of the Rainbow hydrothermal field, Mid-Atlantic Ridge

Petrological, geochemical, and Nd isotopic analyses have been carried out on rock samples from the Rainbow vent field to assess the evolution of the hydrothermal system. The Rainbow vent field is an ultramafic-hosted hydrothermal system located on the Mid-Atlantic Ridge characterized by vigorous high-temperature venting (∼365°C) and unique chemical composition of fluids: high chlorinity, low pH and very high Fe, and rare earth element (REE) contents (Douville et al., Chemical Geology 184:37–48, 2002). Serpentinization has occurred under a low-temperature (<270°C) retrograde regime, later overprinted by a higher temperature sulfide mineralization event. Retrograde serpentinization reactions alone cannot reproduce the reported heat and specific chemical features of Rainbow hydrothermal fluids. The following units were identified within the deposit: (1) nonmineralized serpentinite, (2) mineralized serpentinite—stockwork, (3) steatite, (4) semimassive sulfides, and (5) massive sulfides, which include Cu-rich massive sulfides (up to 28wt% Cu) and Zn-rich massive sulfide chimneys (up to 5wt% Zn). Sulfide mineralization has produced significant changes in the sulfide-bearing rocks including enrichment in transition metals (Cu, Zn, Fe, and Co) and light REE, increase in the Co/Ni ratios comparable to those of mafic Cu-rich volcanic-hosted massive sulfide deposits and different ¹⁴³Nd/¹⁴⁴Nd isotope ratios. Vent fluid chemistry data are indicative of acidic, reducing, and high temperature conditions at the subseafloor reaction zone where fluids undergo phase separation most likely under subcritical conditions (boiling). An explanation for the high chlorinity is not straightforward unless mixing with high salinity brine or direct contribution from a magmatic Cl-rich aqueous fluid is considered. This study adds new data, which, combined with the current knowledge of the Rainbow vent field, brings compelling evidence for the presence, at depth, of a magmatic body, most likely gabbroic, which provides heat and metals to the system. Co/Ni ratios proved to be good tools used to discriminate between rock units, degree of sulfide mineralization, and positioning within the hydrothermal system. Deeper units have Co/Ni <1 and subsurface and surface units have Co/Ni >1.     

Metal sources of the Navan carbonate-hosted base metal deposit, Ireland: Nd and Sr isotope evidence for deep hydrothermal convection

Nd and Sr isotope analyses are presented for gangue mineral samples from the giant carbonate-hosted Navan Zn–Pb deposit, Ireland, and for rocks from which Navan metals may have been derived. Analysis of gangue minerals spanning the Navan paragenetic sequence reveals systematic evolution in the composition of the mineralising fluid. Early fluid represented by replacive dolomite exhibits the lowest initial ⁸⁷Sr/⁸⁶Sr ratio (0.7083–0.7086), closest to that of the host limestone and to Lower Carboniferous seawater, and the highest ¹⁴³Nd/¹⁴⁴Nd ratio (0.51161–0.51176). Later generations of dolomite, barite and calcite, which encompass sulphide precipitation, have higher initial ⁸⁷Sr/⁸⁶Sr ratios (maximum 0.7105) and lower initial ¹⁴³Nd/¹⁴⁴Nd ratios (minimum 0.51157). All samples have initial Nd isotope ratios that are too low to have been acquired only from the host limestone. Drill core samples of presumed Ordovician volcanic and sedimentary rocks from beneath the Navan orebody have ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr ratios at the time of mineralisation of 0.51184–0.51217 and 0.7086–0.7138, respectively. The data are interpreted to indicate mixing of sulphide-rich, limestone-buffered brine, with a metal-bearing hydrothermal fluid, which had passed through sub-Carboniferous rocks, consistent with published fluid inclusion and S isotope data. The ¹⁴³Nd/¹⁴⁴Nd ratio of this basement-derived fluid is too low to have been imparted by flow through the Devonian Old Red Sandstone, as required in models of regional fluid flow in response to Hercynian uplift. Irrespective of whether such regional fluid flow occurred, the hydrothermal Nd must have been derived from sub-Devonian rocks. These conclusions broadly support the hydrothermal convection cell model in which brines, ultimately of surface origin, penetrated to a depth of several kilometres, leaching metals from the rocks through which they passed. The data also support increasing depth of penetration of convection cells with time. Metals were subsequently precipitated in carbonate rocks at sites of mixing with cooler, sulphide-rich fluids. However, comparison of the Navan hydrothermal gangue Nd–Sr isotope data with data from Lower Palaeozoic rocks strongly suggests that the latter cannot alone account for the “basement” signature. As the Navan deposit lies immediately north of the Iapetus Suture, this suggests that the Laurentian margin includes Precambrian basement.     

Secondary Calcification of Planktic Foraminifera from the Indian Sector of Southern Ocean

This study focused on planktic foraminifera in plankton tows and surface sediments from the western Indian sector of Southern Ocean in order to evaluate the potential foraminiferal secondary calcification and/or dissolution in the sediment. It is found that the symbiotic foraminiferal species are abundant in the subtropical region, whereas non-symbiotic species dominate in the sub-Antarctic and polar frontal regions. The distribution of the symbiotic and non-symbiotic foraminiferal species is controlled by temperature, salinity, light, nutrients and phytoplankton biomass. There is also a lateral southern extent in abundance of planktic foraminifera from surface sediments to plankton tows. The shell weights of the planktic foraminifera N. pachyderma, G. bulloides and G. ruber within the surface sediments are on an average heavier by 27%, 34% and 40% respectively than shells of the same size within the plankton tows, indicative of secondary calcification. The planktic foraminiferal isotopes show the presence of heavier isotopes in the surface sediment foraminifera as compared to plankton tows, thus confirming secondary calcification. Secondary calcification in G. ruber occurs in the euphotic zone, whereas in case of N. pachyderma and G. bulloides it is at deeper depths. We also observed a decrease in the shell spines in surface sediment foraminifera as compared to plankton tows, indicative of the morphological changes that foraminifera underwent during gametogenesis.     

安徽南部桃冲地区铁矿床控矿构造分析

通过对桃冲地区典型铁矿床的赋存环境及构造特征的研究和控矿因素分析,认为红花山背斜两翼的铁矿体产于背斜的层间断裂带中的次级褶曲内,受"碳酸盐岩地层+次级褶曲+层间断裂带"三个控矿因素的制约,环滨江岩体的铁矿床受厚层状矽卡岩接触带的制约。综合桃冲地区控矿因素的特点,提出了找矿有利部位。     

一种新的、快速的碳、氮、硫同位素测定手段──EA－IRMS连线分析技术

一种新的、快速的碳、氮、硫同位素测定手段──ＥＡ－ＩＲＭＳ连线分析技术储雪蕾（中国科学院地质研究所，北京１０００２９）关键词元素分析仪－同位素比值质谱仪，连线分析碳，氮，硫同位素碳、氮、硫三种元素的稳定同位素在地学、生态学、环境科学等领域受到了重视，...     

Nature of the Ore-Forming Fluid at the Quaternary Noya Gold Deposit in Kyushu,Japan

We discuss the nature of the ore-forming hydrothermal fluid in the Noya gold-bearing calcite-quartz-adularia veins of central Kyushu, Japan on the basis of oxygen, carbon, and strontium isotope ratios, and aqueous speciation calculations for the present-day geothermal fluid. The isotopic values of the Noya ore-forming fluid were estimated to be −6.5‰ for δ¹³C and −7.5‰ for δ¹⁸O. The oxygen isotopic equilibrium temperatures for vein calcite are more than 180°C at the bottom of the Noya mineralization zone, and decrease with increasing elevation. As the temperature decreased, the dominant carbon species in the fluid changed from H₂CO₃ to HCO₃^- at about 120°C. The equilibrium temperatures for vein quartz are consistent with the calcite calculations. The carbon and oxygen isotope trends of the Noya vein calcite and the isotope ratios of strontium suggest that the fluids that precipitated the Noya veins were controlled by an andesite-dominated geology. Chondrite-normalized REE patterns for the white-colored veins from wells 51-WT-1 and 51-WT-2 displayed a light REE-rich pattern with positive Eu anomalies, suggesting the existence of a reducing environment for the fluid. The pyrite-rich gray-colored veins and a silicified rock from well 51-WT-2 showed higher REE concentrations than did the white veins. Altered host andesitic rocks have similar REE patterns to that of the silicified rock, and have higher REE contents than the others in the drill cores. Aqueous speciation calculations showed that the fluid in the hydrothermal reservoir is currently in muscovite stability. The fluid at the ore-mineralization stage may have contained more potassium or have had a higher pH, so that adularia precipitated with calcite and quartz, as well as gold. Fluid boiling at depth in the system produced the gold-bearing calcite-quartz-adularia veins.     

Long-Term Observations of Isotope Ratio Accuracy and Reproducibility Using Quadrupole ICP-MS

High precision isotope ratio and trace element determination can be achieved with modern quadrupole ICP-MS provided that short and long-term instrument performance is accurately monitored. Here we present results for the isotope ratios ⁶Li/⁷Li, ¹⁴⁷Sm/¹⁴⁹Sm, ¹⁶⁰Dy/¹⁶¹Dy, ²⁰⁷Pb/²⁰⁶Pb, ²⁰⁸Pb/²⁰⁶Pb, ²⁰⁶Pb/²⁰⁴Pb and ²³⁵U/²³⁸U with which we determined long-term isotope ratio stability of relevance to both trace element and isotope determination. With respect to trace element determination, we first present long-term observations regarding oxide formation rates of Ba and Nd on light REE and heavy REE, as well as Zr on Ag. These showed good correlations and could be used to correct effectively the interference. The efficacy of this correction was demonstrated with analyses of the rock reference material BHVO-2 at both low and high oxide formation rates. Next, we studied the long-term reproducibility of a Dy isotope ratio that was measured to correct for the isobaric interference on Gd. It was found that, regardless of tuning condition, the ratio reproduced very well (0.58% RSD, 1s) and that the estimate of the Gd concentration did not suffer from the large correction (> 10%) caused by the Dy isobar. Long-term reproducibilities of Li, Sm and U isotope ratios, required for accurate mass bias correction when isotopically enriched internal standards of these elements are employed, were measured in the rock reference materials AGV-2 and JA-3 over a time period of up to 3 years. As expected, the Li isotope ratio showed the largest variability (RSD = 7%), but the other two ratios had relative external reproducibilities of only 1.01% (1s, U) and 0.67% (Sm). The mass bias-induced scatter in measurements for Sm and U was so small that the internal standard correction was effective, even for samples with high concentrations of these elements. With regard to Pb-isotope ratio determination, we also present long-term reproducibility for NIST SRM 982, run as an unknown and two accuracy tests for Pb separated from granitoids and from meteorites. It is demonstrated that the obtained ratios, including those involving ²⁰⁴Pb, are accurate relative to MC-ICP-MS determinations and of comparable precision to conventional TIMS analysis. The excellent agreement between all data sets shows the potential of modern quadrupole ICP-MS instrumentation for Pb-isotope determination, particularly for samples with very low Pb content.     

Characteristics and origin of sediment-hosted disseminated gold deposits: a review

Sediment-hosted disseminated gold (SHDG) deposits comprise a major portion of the gold production and reserves in the US. Although presently known to be common only in western North America, SHDG deposits are a significant source of world gold production. These deposits are characterized by extremely fine-grained disseminated gold, hosted primarily by arsenian pyrite. Other metals show very little enrichment although in addition to As, anomalous concentrations of elements such as Sb, Hg, Tl and Ba are utilized as exploration tools. The host rocks are dominantly silty carbonates, but ore concentrations are also present in siliceous and silicified rocks as well as intrusive rocks. Alteration consists of decarbonatization, silicification (jasperoid formation) and argillization, which are arranged both spatially and temporally in that order. Argillic alteration is zoned from kaolinite-dominated cores to sericite-dominated margins. The deposits commonly exhibit significant structural (faults) and stratigraphic (composition/permeability) controls. Until the last few years, SHDG deposits were considered as near-surface, epithermal type deposits in origin. Because of their fine-grained nature and the lack of macroscopic features such as veins, it has proven quite difficult to extract geochemical data that are clearly related to their genesis. However, fluid inclusion data indicate pressures corresponding to depths of 2–4 km under lithostatic conditions. Temperatures are constrained by fluid inclusions and phase equilibria to near 225°C. Stable isotope data from alteration minerals and fluid inclusions indicate that the ore fluids were dominated by meteoric waters, some of which had clearly exchanged oxygen with wallrocks during their passage through the crust. Although the data vary, most ore fluids probably had δD values near −150‰ and δ¹⁸O values ranging from −10 to +5‰. Sulfur isotope values reported from SHDG deposits span a wide range, from −30 to +20‰ (sulfides) and 0 to >45‰ (sulfates). Ore-related sulfides (pyrite, realgar) fall at the upper end of the range reported for sulfides. The alteration and mineral assemblage indicate the ore fluids were probably near neutral and gold was likely carried as a bisulfide complex. The depositional mechanism(s) probably included mixing, cooling and oxidation. These mechanisms are consistent with the observed alteration features, i.e. quartz precipitation, calcite dissolution and sericite-kaolinite coexistence. It also explains the presence of both siliceous ores containing native Au and sulfide ores containing Au in pyrite. The extreme variations in sulfur isotopes as seen at Post and fluid inclusion data from Carlin may be indicative of some phase separation (‘boiling’), but such relations have not been documented in other deposits and the importance of phase separation to gold deposition appears minimal.     

Dominant amphipods of Posidonia oceanica seagrass meadows display considerable trophic diversity

Gut content examination and trophic markers (fatty acids, stable isotopes of C and N) were combined to delineate the diet of the dominant species of amphipods from Mediterranean Posidonia oceanica seagrass meadows and to highlight trophic diversity among this community. Our results indicate that, although all dominant species heavily relied on macroalgal epiphytes, considerable interspecific dietary differences existed. Carbon stable isotope ratios notably showed that some of the amphipod species favored grazing on epiphytes from leaves or litter fragments (Apherusa chiereghinii, Aora spinicornis, Gammarus aequicauda), while others such as Dexamine spiniventris preferred epiphytes from rhizomes. The remaining amphipods (Caprella acanthifera, Ampithoe helleri and Gammarella fucicola) readily consumed both groups. In addition, SIAR modeling suggested that most species had a mixed diet, and relied on several food items. Fatty acid analysis and gut contents revealed that contributions of microepiphytic diatoms and of benthic and suspended particulate organic matter to the diet of amphipods were anecdotal. None of the examined species seemed to graze on their seagrass host [low 18:2(n‐6) and 18:3(n‐3) fatty acids contents], but Gammarus aequicauda partly relied on seagrass leaf detritus, as demonstrated by the lesser ¹³C‐depletion of their tissues. Overall, our findings suggest that amphipods, because of their importance in the transfer of organic matter from primary producers and detritus to higher rank consumers, are key items in P. oceanica‐associated food webs.