Hydrothermal alteration and zeolitization of the Fohberg phonolite,Kaiserstuhl Volcanic Complex,Germany

The subvolcanic Fohberg phonolite (Kaiserstuhl Volcanic Complex, Germany) is an economic zeolite deposit, formed by hydrothermal alteration of primary magmatic minerals. It is mined due to the high (>40 wt%) zeolite content, which accounts for the remarkable zeolitic physicochemical properties of the ground rock. New mineralogical and geochemical studies are carried out (a) to evaluate the manifestation of hydrothermal alteration, and (b) to constrain the physical and chemical properties of the fluids, which promoted hydrothermal replacement. The alkaline intrusion is characterized by the primary mineralogy: feldspathoid minerals, K-feldspar, aegirine–augite, wollastonite, and andradite. The rare-earth elements-phase götzenite is formed during the late-stage magmatic crystallization. Fluid-induced re-equilibration of feldspathoid minerals and wollastonite caused breakdown to a set of secondary phases. Feldspathoid minerals are totally replaced by various zeolite species, calcite, and barite. Wollastonite breakdown results in the formation of various zeolites, calcite, pectolite, sepiolite, and quartz. Zeolites are formed during subsolidus hydrothermal alteration (<150 °C) under alkaline conditions. A sequence of Ca–Na-dominated zeolite species (gonnardite, thomsonite, mesolite) is followed by natrolite. The sequence reflects an increase in \(\log [(a_{{{\text{Na}}^{ + } }} )/(a_{{{\text{H}}^{ + } }} )]\) and decrease in \(\log [(a_{{{\text{Ca}}^{2 + } }} )/(a_{{{\text{H}}^{ + } }}^{2} )]\) of the precipitating fluid. Low radiogenic ⁸⁷Sr/⁸⁶Sr values indicate a local origin of the elements necessary for secondary mineral formation from primary igneous phases. In addition, fractures cut the intrusive body, which contain zeolites, followed by calcite and a variety of other silicates, carbonates, and sulfates as younger generations. Stable isotope analysis of late-fracture calcite indicates very late circulation of meteoric fluids and mobilization of organic matter from surrounding sedimentary units.     

Co-diagenesis of iron and phosphorus in hydrothermal sediments from the southern East Pacific Rise: Implications for the evaluation of paleoseawater phosphate concentrations

We present a detailed study of the co-diagenesis of Fe and P in hydrothermal plume fallout sediments from ∼19°S on the southern East Pacific Rise. Three distal sediment cores from 340-1130 km from the ridge crest, collected during DSDP Leg 92, were analysed for solid phase Fe and P associations using sequential chemical extraction techniques. The sediments at all sites are enriched in hydrothermal Fe (oxyhydr)oxides, but during diagenesis a large proportion of the primary ferrihydrite precipitates are transformed to the more stable mineral form of goethite and to a lesser extent to clay minerals, resulting in the release to solution of scavenged P. However, a significant proportion of this P is retained within the sediment, by incorporation into secondary goethite, by precipitation as authigenic apatite, and by readsorption to Fe (oxyhydr)oxides. Molar P/Fe ratios for these sediments are significantly lower than those measured in plume particles from more northern localities along the southern East Pacific Rise, and show a distinct downcore decrease to a depth of ∼12 m. Molar P/Fe ratios are then relatively constant to a depth of ∼35 m. The Fe and P speciation data indicate that diagenetic modification of the sediments is largely complete by a depth of 2.5 m, and thus depth trends in molar P/Fe ratios can not solely be explained by losses of P from the sediment by diffusion to the overlying water column during early diagenesis. Instead, these sediments are likely recording changes in dissolved P concentrations off the SEPR, possibly as a result of redistribution of nutrients in response to changes in oceanic circulation over the last 10 million years. Furthermore, the relatively low molar P/Fe ratios observed throughout these sediments are not necessarily solely due to losses of scavenged P by diffusion to the overlying water column during diagenesis, but may also reflect post-depositional oxidation of pyrite originating from the volatile-rich vents of the southern East Pacific Rise. This study suggests that the molar P/Fe ratio of oxic Fe-rich sediments may serve as a proxy of relative changes in paleoseawater phosphate concentrations, particularly if Fe sulfide minerals are not an important component during transport and deposition.     

A review of the geodynamic setting of large-scale Late Mesozoic gold mineralization in the North China Craton: an association with lithospheric thinning

Abundant gold deposits are distributed along the margins of the North China Craton (NCC). Occurring throughout the Precambrian basement and located in or proximal to Mesozoic granitoids, these deposits show a consistent spatial–temporal association with Late Jurassic–Early Cretaceous magmatism and are characterized by quartz lode or disseminated styles of mineralization with extensive alteration of wall rock. Their ages are mainly Early Cretaceous (130–110 Ma) and constrain a very short period of metallogenesis. Sr–Nd–Pb isotopic tracers of ores, minerals and associated rocks indicate that gold and associated metals mainly were derived from multi-sources, i.e., the wall rocks (Precambrian basement and Mesozoic granites) and associated mafic rocks.Previous studies, including high surface heat flow, uplift and later basin development, slow seismic wave speeds in the upper mantle, and a change in the character of mantle xenoliths sampled by Paleozoic to Cenozoic magmas, have been used to suggest that ancient, cratonic mantle lithosphere was removed from the base of the NCC some time after the Ordovician, and replaced by younger, less refractory lithospheric mantle. The geochemistry and isotopic compositions of the mafic rocks associated with gold mineralization (130–110 Ma) indicate that they were derived from an ancient enriched lithospheric mantle source; whereas, the mafic dikes and volcanic rocks younger than 110 Ma were derived from a relatively depleted mantle source, i.e., asthenospheric mantle. According to their age and sources, relation to magmatism and geodynamic framework, the gold deposits were formed during lithospheric thinning. The removal of lithospheric mantle and the upwelling of new asthenospheric mantle induced partial melting and dehydration of the lithospheric mantle and lower crust due to an increase of temperature. The fluids derived from the lower crust were mixed with magmatic and meteoric waters, and resulted in the deposition of gold and associated metals.     

黑龙江杂岩的碎屑锆石年代学及其大地构造意义

黑龙江杂岩带位于佳木斯地体西缘,为佳木斯地体向西与松嫩地体之间俯冲、拼贴、碰撞而形成的高压变质带.黑龙江杂岩沿牡丹江断裂分布,其构造-岩石组合、变质变形特征等显示其为佳木斯地体向松嫩地体俯冲拼帖的过程中形成的增生杂岩,目前保存下来的杂岩带应为大规模增生楔仰冲到佳木斯地体之上的残余部分.88颗碎屑锆石的全部样品SHRIMPU-Ph年代学测试结果显示三个主要年龄区间:170～220Ma,峰值年龄为183Ma;240～338Ma,峰值年龄为256Ma;450～520Ma,峰值年龄为470Ma.而28个碎屑锆石谐和年龄的年龄谱为两组:240～338Ma,峰值年龄为256Ma;450～500Ma,峰值年龄为470Ma.碎屑锆石年龄数据分析得到,240～338Ma峰期年龄为256Ma的年龄应代表黑龙江杂岩主体岩石的沉积年龄上限;而450～500Ma的年龄谱对应于佳木斯地体的基底变质岩年龄,显示佳木斯地体的基底变质岩曾为黑龙江杂岩的物源区;而170～210Ma,峰期年龄为183Ma的不谐和年龄应为受印支期-早侏罗世构造热事件的扰动年龄,与该区变质单矿物的Ar-Ar年龄相一致,应代表了该区陆-陆碰撞的时代.上述年龄为黑龙江杂岩的形成与演化提供了重要的地质年代学制约,即黑龙江杂岩的原岩成岩时代上限为早三叠世,佳木斯地体向西的俯冲时代主体为印支期,而陆-陆拼贴及碰撞过程主要为晚印支期并可能持续到早侏罗世.这些结果将为揭示我国东北地区构造演化的年代学格架以及三叠纪古亚洲构造域向环太平洋构造域叠加和转换的动力学背景研究提供新的基本地质事实依据.     

山西五台山-恒山地区晚太古-早元古代若干关键地质问题的再认识:单颗粒锆石离子探针质谱年龄提出的地质制约

大量准确度很高的单颗粒锆石迅谱(SHRIMP)年代学数据表明,五台山-恒山绿岩带形成于2500Ma之前,五台山-恒山绿岩带形成后即与较老的阜平块体拼合。因此,该过程中有大量火山,深成活动及变质作用,是一次重要的造山运动。在1800Ma之前,本区还经历了一次明显的构造热事件,主要表现为在地壳较深水平上大规模的冲断作用,使原来为不同地壳水平的块体处于同一地壳水平。本文还对原五台群下部层位板峪口组和金岗库组的归属及铁堡不整合面提出了新的看法。     

内蒙古苏尼特左旗南两类花岗岩同位素年代学及其构造意义

内蒙古北部索伦缝合带（索伦-苏尼特左旗-锡林浩特）被多数中外学者认为是西伯利亚板块南缘和华北板块北缘的最终缝合带,本文选择该缝合带上苏尼特左旗南两类花岗岩-与俯冲有关和与碰撞有关的岩浆岩（分别叫弧岩浆岩和碰撞岗岩）进行同位素年代学研究,结果表明：（1）弧岩浆活动有两期,分别约为490Ma和310Ma(锆石U-Pb,SHRIMP);碰撞花岗岩的侵位年代在230-250Ma(Rb-Sr全岩和锆石U-Pb);（2）根据本文新的年代学数据,索伦缝合带的最终缝合时间可能是在230-310Ma,这显然不同于国内多数学者坚持的“晚泥盆世碰撞”模式;而Sengor等推测的“晚二又开展碰撞”模式与本文数据一致。     

Ecosystem response to antibiotics entering the aquatic environment

Awareness of antibiotics in wastewaters and aquatic ecosystems is growing as investigations into alternate pollutants increase and analytical techniques for detecting these chemicals improve. The presence of three antibiotics (ciprofloxacin, norfloxacin and cephalexin) was evaluated in both sewage effluent and environmental waters downstream from a sewage discharge. Bacteria cultured from the sewage bioreactor and receiving waters were tested for resistance against six antibiotics (ciprofloxacin, tetracycline, ampicillin, trimethoprim, erythromycin and trimethoprim/sulphamethoxazole) and effects of short term exposure (24 h) to antibiotics on bacterial denitrification rates were examined. Antibiotics were detected entering the sewage treatment plant with varying levels of removal during the treatment process. Antibiotics were also detected in effluent entering receiving waters and detectable 500 m from the source. Among the bacteria cultured from the sewage bioreactor, resistance was displayed against all six antibiotics tested and bacteria cultured from receiving waters were resistant against two of the antibiotics tested. Rates of denitrification were observed to decrease in response to some antibiotics and not to others, though this was only observed at concentrations exceeding those likely to be found in the environment. Findings from this preliminary research have indicated that antibiotics are entering our aquatic systems and pose a potential threat to ecosystem function and potentially human health.     

Linking gold mineralization to regional-scale drivers of mineral systems using in situ U–Pb geochronology and pyrite LA-ICP-MS element mapping

Proterozoic orogens commonly host a range of hydrothermal ores that form in diverse tectonic settings at different times. However, the link between mineralization and the regional-scale tectonothermal evolution of orogens is usually not well understood, especially in areas subject to multiple hydrothermal events.Regional-scale drivers for mineral systems vary between the different classes of hydrothermal ore, but all involve an energy source and a fluid pathway to focus mineralizing fluids into the upper crust. The Mount Olympus gold deposit in the Proterozoic Capricorn Orogen of Western Australia, was regarded as an orogenic gold deposit that formed at ca. 1738 Ma during the assembly of Proterozoic Australia. However,the trace element chemistry of the pyrite crystals closely resembles those of the Carlin deposits of Nevada,with rims that display solid solution gold accompanied by elevated As, Cu, Sb, Hg, and Tl, surrounding gold-poor cores. New SHRIMP UeP b dating of xenotime intergrown with auriferous pyrite and ore-stage alteration minerals provided a weighted mean~(207) Pb*/~(206) Pb* date of 1769 ± 5 Ma, interpreted as the age of gold mineralization. This was followed by two discrete episodes of hydrothermal alteration at 1727 ± 7 Ma and 1673 ± 8 Ma. The three ages are linked to multiple reactivation of the crustal-scale Nanjilgardy Fault during repeated episodes of intracratonic reworking. The regional-scale drivers for Carlin-like gold mineralization at Mount Olympus are related to a change in tectonic regime during the final stages of the intracratonic 1820 -1770 Ma Capricorn Orogeny. Our results suggest that substantial sized Carlin-like gold deposits can form in an intracratonic setting during regional-scale crustal reworking.     

Geochemistry, Geochronology and Isotopic Evolution of the Chewore-Rufunsa Terrane, Southern Irumide Belt: a Mesoproterozoic Continental Margin Arc

The southern Irumide Belt (SIB) is an ENE–WSW-trending,late Mesoproterozoic orogenic belt located between the Congo–Tanzania–Bangweulu(CTB) and Kalahari cratons in central southern Africa. It isseparated from the late Mesoproterozoic Irumide Belt (IB) tothe north by Permo-Triassic graben, raising the possibilitythat the younger rifts reactivated a suture between the twobelts that has been rendered cryptic as a result of youngerKaroo cover. Both belts are dominated by calc-alkaline gneisses,but in addition the SIB contains abundant metavolcanic and metasedimentaryrocks. In this study we present detailed geochemical, isotopicand geochronological data for volcanic and plutonic lithologiesfrom the southernmost part of the SIB, the Chewore–RufunsaTerrane. This terrane comprises a wide variety of supracrustalto mid-crustal rocks that have major- and trace-element compositionssimilar to magmas formed in present-day subduction zones. Chondrite-normalizedrare earth element (REE) profiles and whole-rock Sm–Ndisotope compositions indicate that the parental supra-subductionmelts interacted with, and were contaminated by sialic continentalcrust, implying a continental-margin-arc setting. Secondaryionization mass spectrometry dating of magmatic zircon has yieldedcrystallization ages between c. 1095 and 1040 Ma, similar toelsewhere in the SIB. U–Pb dating and in situ Lu–Hfisotopic analyses of abundant xenocrystic zircon extracted fromthe late Mesoproterozoic granitoids indicate that the contaminantcontinental basement was principally Palaeoproterozoic in ageand had a juvenile isotopic signature at the time of its formation.These data are in contrast to those for the IB, which is characterizedby younger, c. 1020 Ma, calc-alkaline gneisses that formed bythe direct recycling of Archaean crust without significant additionof any juvenile material. We suggest that the SIB developedby the subduction of oceanic crust under the margin of an unnamedcontinental mass until ocean closure at c. 1040 Ma. Subsequentcollision between the SIB and the CTB margin led to the cessationof magmatism in the SIB and the initiation of compression andcrustal melting in the IB. KEY WORDS: geochemistry; Mesoproterozoic; SHRIMP zircon U–Pb dating; Sm–Nd isotopes; Southern Irumide Belt     

Low‐temperature thermochronology of francolite: Insights into timing of Dead Sea Transform motion

Cambrian siliciclastic sequences along the Dead Sea Transform (DST) margin in southern Israel and southern Jordan host both detrital fluorapatite [D‐apatite] and U‐rich authigenic carbonate‐fluorapatite (francolite) [A‐apatite]. D‐apatite and underlying Neoproterozoic basement apatite yield fission‐track (FT) data reflecting Palaeozoic–Mesozoic sedimentary cycles and epeirogenic events, and dispersed (U–Th–Sm)/He (AHe) ages. A‐apatite, which may partially or completely replace D‐apatite, yields an early Miocene FT age suggesting formation by fracturing, hydrothermal fluid ascent and intra‐strata recrystallisation, linked to early DST motion. The DST, separating the African and Arabian plates, records ~105 km of sinistral strike‐slip displacement, but became more transtensional post‐5 Ma. Helium diffusion measurements on A‐apatite are consistent with thermally activated volume diffusion, indicating Tc ~52 to 56 ± 10°C (cooling rate 10°C/Ma). A‐apatite AHe data record Pliocene cooling (~35 to 40°C) during the transtensional phase of movement. This suggests that timing of important milestones in DST motion can be discerned using A‐apatite low‐temperature thermochronology data alone.