REE geochemistry of some alkali-rich intrusive rocks in China

Based on the REE analyses of about 300 samples from 40 alkali-rich intrusive rocks, a systematic study on the features of REE composition was made, and the major factors controlling the REE distribution are discussed. According to REE, trace elements composition and Sr, Nd isotopic characteristics, the source materials and petrogenetic process of the alkali-rich intrusive rocks were studied. The petrogenetic models of Zijinshan, Sairna, Nianzishan and Shanhaiguan alkali-rich intrusive rocks were calculated using multisequence fractional crystallization and assimilation fractional crystallization models. Project supported by the President Foundation of Chinese Academy of Sciences.     

Formation of Fe-oxyhydroxides from the East Pacific Rise near latitude 13°N: Evidence from mineralogical and geochemical data

The mineralogical and geochemical characteristics of Fe-oxyhydroxide samples from one dredge station (long. 103°54.48′W, lat. 12°42.30′N, water depth 2655 m) on the East Pacific Rise near lat 13°N were analyzed by XRD, ICP-AES, and ICP-MS. Most Fe-oxyhydroxides are amorphous, with a few sphalerite microlites. In comparison with Fe-oxyhydroxides from other fields, the variable ranges in the chemical composition of Fe-oxyhydroxide samples are very narrow; their Fe, Si, and Mn contents were 39.90%, 8.92%, and 1.59%, respectively; they have high Cu (0.88%–1.85%) and Co (65×10⁻⁶−704×10⁻⁶) contents, and contain Co+Cu+Zn+Ni> 1.01%. The trace-element (As, Co, Ni, Cu, Zn, Ba, Sr) and major-element (Fe, Ca, Al, Mg) contents of these samples are in the range of hydrothermal sulfide from the East Pacific Rise near 13°N, reflecting that this type of Fe-oxyhydroxide constitutes a secondary oxidation product of hydrothermal sulfide. The Fe-oxyhydroxide samples from one dredge station on the East Pacific Rise near 13°N are lower in ΣREE (5.44×10⁻⁶–17.01×10⁻⁶), with a distinct negative Ce anomaly (0.12–0.28). The Fe-oxyhydroxide samples have similar chondrite-normalized rare-earth-element (REE) patterns to that of seawater, and they are very different from the REE composition characteristics of hydrothermal plume particles and hydrothermal fluids, showing that the REEs of Fe-oxyhydroxide are a major constituent of seawater and that the Fe-oxyhydroxides can become a sink of REE from seawater. The quick settling of hydrothermal plume particles resulted in the lower REE content and higher Mn content of these Fe-oxyhydroxides, which are captured in part of the V and P from seawater by adsorption. The Fe-oxyhydroxides from one dredge station on the East Pacific Rise near 13°N were formed by secondary oxidation in a low temperature, oxygenated environment. In comparison with the elemental (Zn, Cd, Pb, Fe, Co, Cu) average content of hydrothermal sulfide samples from the East Pacific Rise near 13°N, the Zn, Cd, and Pb contents of the Fe-oxyhydroxides are lower, and their Fe, Co, and Cu contents are higher. Supported in part by the Pilot Project of Knowledge Innovation Project, Chinese Academy of Sciences (Grant No. KZCX3-SW-223), and the Special Foundation for the Tenth Five Plan of COMRA (Grant No. DY105-01-03-1)     

Rare earth and strontium isotope evidence concerning the petrogenesis of North Chilean ignimbrites

New rare earth element (REE) data, Rb and Sr analyses and Sr isotope measurements are presented for pumice clasts collected from some North Chilean ignimbrites of dacite and rhyolite composition. The samples are light-REE enriched with chondrite-normalised Ce (Ce_N) of 17–98, Yb_N of 4–14 and Ce_N/Yb_N of 2.6–15. While some samples have no Eu anomalies, others do have anomalies with inferred Eu/Eu^* values of down to ca. 0.4. Eleven samples have present-day⁸⁷Sr/⁸⁶Sr ratios between 0.7053 and 0.7100, and noting that some samples are up to 12 Ma old, initial⁸⁷Sr/⁸⁶Sr ratios are below ca. 0.709. These trace element and Sr isotope characteristics resemble those of contemporaneous andesite and dacite lavas, suggesting a common origin for all these rock types. The higher Rb/Sr ratios and larger Eu anomalies in most of the dacitic and rhyolitic ignimbrites are consistent with an origin by plagioclase-dominated fractional crystallization of mantle-derived andesite magma.     

143Nd/144Nd,87Sr/86Sr and trace element constraints on the petrogenesis of Aleutian island arc magmas

¹⁴³Nd/¹⁴⁴Nd,⁸⁷Sr/⁸⁶Sr and trace element results are reported for volcanic and plutonic rocks of the Aleutian island arc. The Nd and Sr isotopic compositions plot within the mantle array with ε_Nd values of from 6.5 to 9.1 and⁸⁷Sr/⁸⁶Sr ratios of from 0.70289 to 0.70342. Basalts have mildly enriched light REE abundances but essentially unfractionated heavy REE abundances, while andesites exhibit a greater degree of light to heavy REE fractionation. Both the basalts and andesites have significant large ion lithophile element to light rare earth element (LILE/LREE) enrichments. Variations in the isotopic compositions of Nd and Sr are not related to the spatial distribution of volcanoes in the arc, nor are they related to temporal differences. ε_Nd and⁸⁷Sr/⁸⁶Sr do not correlate with major element compositions but do, however, correlate with certain LILE/LREE ratios (e.g. Ba_N/La_N). Plutonic rocks have isotropic and trace element characteristics identical to some of the volcanic rocks. Rocks that make up the tholeiitic, calc-alkaline and alkaline series in the Aleutians do not come from isotopically distinct sources, but do exhibit some differing LILE characteristics.Given these elemental and isotopic constraints it is shown that the Aleutian arc magmas could not have been derived directly from homogeneous MORB-type mantle, or fresh or altered MORB subducted beneath the arc. Mixtures of partially altered MORB with deep-sea sediment can in principle account for the isotopic characteristics and most of the observed LILE/LREE enrichments. However, some samples have exceedingly high LILE/LREE enrichments which cannot be accounted for by sediment contamination alone. For these samples a more complex scenario is considered whereby dehydration and partial melting of the subducted slab, containing less than 8% sediment, produces a LILE-enriched (relative to REE) metasomatic fluid which interacts with the overlying depleted mantle wedge. The isotopic and LILE characteristics of the mantle are extremely sensitive to metasomatism by small percentages of added fluid, whereas major elements are not substantially effected, Major element compositions of Aleutian magmas are dominantly controlled by the partial melting of this mantle and subsequent crystal fractionation; whereas isotopic and LILE characteristics are determined by localized mantle heterogeneities.     

Terminal Ediacaran anoxia in deep-ocean: Trace element evidence from cherts of the Liuchapo Formation,South China

Here we report a detailed trace element study of the cherts from Liuchapo Formation, which is a terminal Ediacaran (551-542 Ma) succession in South China deposited in deep-water basinal setting. The REE of Liuchapo cherts shows similar features as observed for anoxic modern seawater (but not for hydrothermal fluids), characterized by positive La anomaly (La_N/Ce_N = 0.83–1.91, average 1.37), moderately negative Ce anomaly (0.53–1.1, average 0.73), positive Gd anomaly (average 1.08), positive Y anomaly (average 1.21), and depleted LREE and MREE. In addition, the Liuchapo cherts have low ΣREE (3.36–56.13 ppm, average 20.6 ppm), low Al₂O₃, Ti, Th and Zr concentrations, and high Y/Ho ratios (up to 43.9). The redox-sensitive trace elements concentrations in the cherts do not correlate with detrital input proxies. All of these features suggest that the redox-sensitive trace elements in the cherts were authigenically concentrated in water column and their concentrations thus are excellent indicators of ancient redox conditions. Very low Th/U ratios, high V/(V+Ni) and Fe_⊤/Al ratios, enrichments of redox-sensitive trace elements (U, V, Mo), and low concentration of Mn in the cherts imply anoxia in the deep seawater. Our data reveal that the terminal Ediacaran ocean was not completely oxidized and the deep ocean was still anoxic, at least in South China. We propose that although the oxidative events existed in the terminal Ediacaran oceans, decomposition of organic matter prolonged anoxia in the deep ocean. Supported by National Natural Science Foundation of China (Grants Nos. 40532012, 40873007, 40603021) and Chinese Academy of Sciences (Grant No. KZCX3-SW-141)     

Element enrichment and U-series isotopic characteristics of the hydrothermal sulfides at Jade site in the Okinawa Trough

The geochemical and U-series isotopic characteristics of hydrothermal sulfide samples from the Jade site (127°04.5′E, 27°15′N, water depth 1300–1450 m) at Jade site in the Okinawa Trough were analyzed. In the hydrothermal sulfide samples bearing sulfate (samples HOK1 and HOK2), the LREEs are relatively enriched. All the hydrothermal sulfide samples except HOK1 belong to Zn-rich hydrothermal sulfide. In comparison with Zn-rich hydrothermal sulfides from other fields, the contents of Zn, Pb, Ag, Cd, Au and Hg are higher, the contents of Fe, Al, Cr, Co, Ni, Sr, Te, Cs, Ti and U lower, and the ²¹⁰Pb radioactivity ratios and ²¹⁰Pb/Pb ratios very low. In the hydrothermal sulfide mainly composed of sphalerite, the correlations between rare elements Hf and U, and Hf and Mn as well as that between dispersive elements Ga and Zn, are strongly positive; also the contents of Au and Ag are related to Fe-sulfide, because the low temperature promotes enrichment of Au and Ag. Meanwhile, the positive correlations between Fe and Bi and between Zn and Cd are not affected by the change of mineral assemblage. Based on the ²¹⁰Pb/Pb ratios of hydrothermal sulfide samples (3.99×10⁻⁵-5.42×10⁻⁵), their U isotopic composition (²³⁸U content 1.15–2.53 ppm, ²³⁸U activity 1.07–1.87 dpm/g, ²³⁴U activity 1.15–2.09 dpm/g and ²³⁴U/²³⁸U ratio 1.07–1.14) and their ²³²Th and ²³⁰Th contents are at base level, and the chronological age of hydrothermal sulfide at Jade site in the Okinawa Trough is between 200 and 2000 yr. Supported by the Pilot Project of Knowledge Innovation Project, Chinese Academy of Sciences (Grant No. KZCX2-YW-211), National Natural Science Foundation of China (Grant Nos. 40830849, 40176020), and Special Foundation for the Eleventh Five Plan of COMRA (Grant No. DYXM-115-02-1-03)     

Cherts from the Yangla copper deposit, western Yunnan Province: geochemical characteristics and relationship with massive sulfide mineralization

Four layers of cherts were found for the first time in the Yangla copper deposit, western Yunnan Province. The cherts possessed the following geochemical characteristics: 1 Low TiO₂ and Al₂O₃ contents, but high ore-forming element (e.g. Cu, Au, Ag) contents; 2 low total REE contents and clear negative Eu anomalies when normalized to chondrite similar to the REE contents and distribution patterns of associated massive sulfide ores; 3 silicon isotopic compositions of cherts in the Yangla deposit being the same as cherts and geyserite of hot-water sedimentary origin; 4 lead and sulfur isotopic compositions of cherts in the Yangla deposit being similar to those of the massive sulfide ores in the Yangla deposit; 5 Rb-Sr isochron age of cherts from the Yangla deposit being identical with that of host strata. Hence, we conclude that the cherts in the Yangla deposit are of hot-water sedimentary origin, which have a close relationship with the massive sulfide ores. The discovery of hydrothermal cherts from the Yangla copper deposit provides further evidence for the hydrothermal exhalative origin of the massive sulfide deposits.     

Organic carbon isotopes of the Sinian and Early Cambrian black shales on Yangtze Platform, China

Organic matter of the Sinian and early Cambrian black shales on the Yangtze Platform belongs to the light carhon group of isotopes with the δ¹³C values from - 27% to - 35 %, which are lower than those of the contempomneously deposited carbonates and phosphorites. A carbon isotope-stratified paleooceanographic model caused by upwelling is proposed, which can be used not only to interpret the characteristies of organic carbon isotopic compositions of the black shales, but also to interpret the paleogeographic difference in the organic carbon isotope compositions of various types of sedimentary rocks. Project supported by the National Natural Science Foundation of China (Grant No. 49472114) and the Open Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences.     

Geochemistry of the Middle to Late Permian limestones from the marginal zone of an isolated platform (Laibin, South China)

Major, trace and rare earth elements were measured in 27 samples of the Middle to Late Permian limestones from the Tieqiao section located on the marginal zone of an isolated platform (Laibin, South China). Shale-normalized REE+Y patterns of all samples show notably negative Ce anomalies (0.21–0.66, average 0.33), slightly positive Gd anomalies (1.08–1.30, average 1.20), and positive Y anomalies with superchondritic Y/Ho ratios (36–91, average 55), which are consistent with those of modern shallow seawater. Their relative LREEs enrichment with higher Nd_SN/Yb_SN ratios (0.58–1.80) than those of modern shallow seawater (0.21–0.50) suggests complicated sources of REEs for all samples. Compared with geochemical features of sediments influenced by terrigenous particles and hydrothermal fluids, it is concluded that ambient shallow seawater was the primary source of REEs in these limestones. Comparing the indicators of REE+Y elements (ΣREE, Nd_SN/Yb_SN, Ce/Ce*, Gd/Gd*, Eu/Eu* and Y/Ho) in limestones with those in bedded cherts from the Tieqiao section, we consider that limestone and bedded chert have similar sources of REE+Y elements: ambient shallow seawater with more or less hydrothermal fluids. In addition, there is a completely negative correlation between CaCO₃ and SiO₂ contents in limestones and bedded cherts. These results imply that precipitation of CaCO₃ was inhibited by that of SiO₂ which was derived mainly from hydrothermal fluid, especially in bedded cherts from the Tieqiao section.     

The mineralogy and the isotopic composition of sulfur in hydrothermal sulfide/sulfate deposits on the East Pacific Rise, 21°N latitude

The mineralogy of five groups of hydrothermal chimneys from the East Pacific Rise has been examined. Three of the chimneys, where the exit temperature of the hydrothermal fluids was close to 350°C, are rich in copper sulfides. Exit temperatures from the other two chimneys were less than 300°C; in these, the chimney walls are rich in zinc sulfide. The major sulfides in the chimneys as a whole were found to be wurtzite, chalcopyrite, pyrite, and cubanite. Anhydrite is always the dominant sulfate, and is present in all the deposits. Silicates are also present but in relatively minor amounts. There are considerable differences in the mineralogy of sulfides, sulfates, and silicates between the active and inactive vent deposits.The isotopic composition of sulfur in anhydrites from active vents is close to that of seawater; the δ³⁴S values of the sulfides range from +1.3 to +4.1‰. The isotopic composition of sulfur in the anhydrites is consistent with a derivation predominantly from seawater sulfate. The sulfur in the sulfides must have a complex origin including contributions from both sulfur in basalts and sulfide produced by reduction of sulfate in seawater. Mixing of H₂S-dominated hydrothermal fluids with cold seawater near the seafloor resulted in the precipitation of non-equilibrium assemblages of sulfides and sulfates.     

Boron isotopic fractionation in laboratory inorganic carbonate precipitation: evidence for the incorporation of B(OH)<Subscript>3</Subscript> into carbonate

A laboratory inorganic carbonate precipitation experiment at high pH of 8.96 to 9.34 was conducted, and the boron isotopic fractionations of the precipitated carbonate were measured. The data show that boron isotopic fractionation factors (α_carb-3) between carbonate and B(OH)₃ in seawater range 0.937 and 0.965, with an average value of 0.953. Our results together with those reported by Sanyal and collaborators show that the α_carb-3 values between carbonate and B(OH)₃ in solution are not constant but are negatively correlated with the pH of seawater. The measured boron isotopic compositions of carbonate precipitation (δ¹¹B_carb) do not exactly lie on the best-fit theoretical δ¹¹B₄-pH curves and neither do they exactly parallel any theoretical δ¹¹B₄-pH curves. Therefore, it is reasonable to argue that a changeable proportion of B(OH)₃ with pH of seawater should also be incorporated into carbonate except for the dominant incorporation of B(OH)₄ ⁻ in carbonate. Hence, in the reconstruction of the paleo-pH of seawater from boron isotopes in marine biogenic carbonates, the use of theoretical boron isotopic fractionation factor (α₄₋₃) between B(OH)₄ ⁻ and B(OH)₃ is not suitable. Instead, an empirical equation should be established. Supported by National Natural Science Foundation of China (Nos. 40573013 and 40776071), State Key Laboratory of Loess and Quaternary Geology, Institute of Earth Environment, Chinese Academy of Sciences (Grant No SKLLQG0502) and State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences     

Metamorphic characteristics and geotectonic implications of the high-pressure granulites from Namjagbarwa, eastern Tibet

A large area of high-pressure garnet-kyanite granulite is exhumed in the Namjagbarwa area, which provides a window for observing the deep crust rocks and structures of the Tibetan Plateau. Three mineral assemblages can have been distinguished in the garnet-kyanite HP granulites by petrography, i.e. M₁. Mus+Bi+P1+Q, M₂. Gt+Ky +perphite/antiperphite+Rt+Q, M₃. Gt+Sill+Cord+Sp+Ilm ± Opx. Metamorphic conditions of the peak granulite assemblages (M₂) formatted by thickening of crusts, with available isotopic ages of 45–69 Ma, are at 1.4—1.8 Gpa and 750—850°. Their retrograde assemblages overprinted by decompressure during the uplift, with available isotopic ages of 18—23 Ma, were formed at 0.60—0.70 Gpa, 621—726°. The thermobarometric evaluation, petrogenetic grid and corresponding isotopic ages indicate a clockwise isothermal decompression metamorphic path. The HP granulite metamorphic history indicates that the collision of the Indian Plate with the Eurasian Plate had begun at 70 Ma, far earlier than the widely accepted 45 Ma. Project supported by the National Natural Science Foundation of China (Grant No. 49732100), the National Key Project for Basic Research, and the Chinese Academy of Sciences Project for Tibetan Research Project (GrantNos. KZ951-A1-204, KZ95T-06).     

Geochemistry and Sr-Nd isotope characteristics of tonalites in Zêtang, Tibet: New evidence for intra-Tethyan subduction

Tonalites from the island arc rock assemblage in the Zêtang segment of the Yarlung Zangbo suture zone were analyzed for major, trace elements (including REE) and Sr-Nd isotope. The experimental datademonstrate that the tonalites have the adakite-like characteristics, including high SiO2 (58%-63%),Al2O3 (18.4%-22.4%), Sr (810×10-6-940×10-6), Sr/Y (77-106), low HREE (Y=9×10-6-11×10-6, Yb=1×10-6-1.3×10-6), with LREE enrichment and faint Eu positive anomaly. Isr (0.70421-0.70487) is relatively low whereas 143Nd/144Nd (0.512896-0.512929) and εNd(t) values ( 6.7- 7.3) are high. These feainvolvement of a small amount of oceanic sediments. The identification of Z(e)tang adakites, derived from slab melting, presents new evidence for the intra-Tethyan subduction and the previous suggestion about the existence of intra-oceanic island arc within Tethys.     

Carbon isotopic composition and its implications on paleoclimate of the underground ancient forest ecosystem in Sihui,Guangdong

We present the carbon isotopic composition of the total organic carbon (TOC) and fine roots in the sedimentary profile from the underground ancient forest in Sihui to study the climatic and environmental changes from 4.5 ka BP to 0.6 ka BP. Results show that C₃ plant was the main vegetation from 4.5 ka BP to 0.6 ka BP in this region. The ancient forest began to develop in the wetland at around 4 ka BP and disappeared together with the wetland at about 3.0 ka BP, implying that the climate had changed greatly at around 3.0 ka BP. As indicated by the simulation results, the content of atmospheric CO₂ increased slightly during 3.5 ka BP to 3.0 ka BP, implying climate warming during that period. The interval of radiocarbon age between 3.0 ka BP to 1.2 ka BP was possibly caused by the strong erosion when the block was lifted in the neotectonic movement. From 1.2 ka BP to 0.6 ka BP, the region remained in terrestrial sedimentary environment, and the surface plant biomass declined gradually. Drought caused by the climate change was the likely cause for the disappearance of the ancient forest. South transition of Intertropical Convergence Zone (ITCZ) was probably the main mechanism for the climate change. Supported by National Natural Science Foundation of China (Grant Nos. 40231015 and 40473002), National Basic Research Program of China (Grant No. 2005CB422004), the Knowledge Innovation Program of the Chinese Academy of Sciences (Grant No. KSCX2-SW-133) and Open Funds of State Key Laboratory of Organic Geochemistry (Grant No. OGL-200607)     

Geochemical anomalies of hydrothermal plume at EPR 13°N

During the DY105-12, 14cruise (R/V DAYANG YIHAO, November 2003) on East Pacific Rise (EPR) 12- 13°N, the submarine hydrothermal activity was investigated and the CTD hydrocast was carried out at EPR12°39′N-12°54′N. From the temperature anomalies and the concentrations of magnesium, chlorine, bromine in seawater samples, we discover that magnesium depletes 9.3%-22.4%, chlorine and bro- mine enrich 10.3%-28.7% and 10.7%-29.0% respectively relative to normal seawater at the stations which have chemistry anomalies, moreover temperature and chemistry anomalies are at the same layer. The depletion of magnesium in the plume may be caused by a fluid lacking of magnesium which rises after the hydrothermal fluid reaches the equilibrium with ambient seawater, the enrichment of chlorine and bromine might be the result of inputting later brine which is generated by phase separation due to hydrothermal activity. In addition, the Br/Cl ratio in the abnormal layers at the survey area is identical to that in seawater, which implies that halite dissolution (or precipitation) occurs neither when the fluid is vented nor when hydrothermal fluid entraining ambient seawater rises to form plume. From the ab- normal instance at E55 station, it is very possible that there might exist a new hydrothermal vent site.     

Petrogenesis of basalts from the FAMOUS area: Mid-Atlantic Ridge

Fresh basalt glasses most of which have Mg/(Mg + Fe²⁺) of 0.66–0.72 from outcrops within 3 km of one other in the rift valley at the Project FAMOUS locality have been analyzed for major, minor and trace elements in order to determine their petrogenesis.Transition metal abundances of the FAMOUS samples are similar to a wide variety of continental and oceanic basalts with high MgO and Ni, all of which show remarkably little variation, with the exception of Cu, Zn and Ti, on a chondrite-normalized plot. Modelling of these data suggests that the mantle beneath both continents and oceans is systematically fractionated relative to chondrites. This fractionation provides a constraint for models of earth formation and subsequent evolution.The abundances of the rare earth and the incompatible elements, Ba, La, Th, U, and Nb, vary by more than a factor of three and the La/Yb and La/Sm ratios vary by factors of 3.1 and 1.6, respectively, in samples with similar, high Mg/(Mg + Fe²⁺). There is no correlation between the degree of light-REE enrichment and the heavy-REE abundance. Furthermore, the trace element variations do not appear correlated with respect to location in the rift valley or to time of eruption. These trace element features demonstrate that successive eruptions in one small area of the rift valley can show wide variations in trace element chemistry over a short span of time; they preclude the derivation of these basalt glasses from a single magma chamber.Despite the heterogeneities in REE and the variable trace element abundances, a homogeneous mantle source is suggested by the similarities among the samples in the incompatible element ratios of La/Ce, Ba/Th, Zr/Nb and K/Ba and the small range in⁸⁷Sr/⁸⁶Sr isotope ratios observed in other samples from the FAMOUS region (White and Bryan, 1977). Thus, trace element heterogeneities appear to be generated by processes in the mantle during melting. However, processes such as batch partial melting, fractional fusion, fractional crystallization, zone refining, or mixing of magmas or sources acting alone are incapable of explaining the lack of correlation between the light and heavy REE.It is suggested that the observed variations are a consequence of dynamic partial melting of a homogeneous mantle source region. This process includes varying degrees of partial melting of an uprising mantle source with continuous but incomplete removal of melt as melting proceeds, varying extents of batch partial melting, and zone refining. Dynamic melting can produce different melts from a homogeneous source which have different degrees of light-REE enrichment and crossing REE patterns. The variable trace element abundances which may be produced through dynamic melting may be the cause of the apparent decoupling of major and trace elements (Bryan et al., 1976) which previously has been suggested for the FAMOUS region (Bryan and Moore, 1977).     

Geochronology of Ailaoshan-Jinshajiang alkalirich intrusive rocks and their Sr and Nd isotopic characteristics

Twenty-nine isotopic ages, ranging from 41 to 27 Ma, are presented for the alkali-rich intrusive rocks and their coexisting alkaline volcanic rocks, lamprophyres and acidic porphyries, indicating that they are Tertiary in age. The alkali-rich intrusive rocks have¹⁴³Nd/¹⁴⁴Nd ratios from 0. 512 415 to 0. 512 544, and⁸⁷Sr/⁸⁶Sr ratios from 0.705 4 to 0.706 8, suggesting that their material originates from an enriched mantle source. Project supported by the National Natural Science Foundation of China and the Special Grant of the President of Chinese Academy of Sciences.     

Origin of the rhyolitic rocks of the taupo volcanic zone, New Zealand

Major element, Rb, Sr, Ba, Cr and V analyses as well as 13 new rare earth element (REE) analyses are presented for the greywacke basement surrounding the Taupo Volcanic Zone (TVZ). On this basis the basement rocks are divided into a Western Basement of approximately andesitic composition ( 62% SiO₂) and an Eastern Basement of approximately granodiorite composition ( 75% SiO₂). These analyses, 5 new REE analyses for the rhyolites, and published data for the volcanic rocks of TVZ are used to investigate the petrogenesis of rhyolitic rocks in the area.Least-squares mixing calculations for major elements show that 88% fractional crystallisation of high-alumina basalt produces a liquid of rhyolitic bulk composition, but Rayleigh fractionation models show that the trace element concentrations of the rhyolites are inconsistent with basalt fractionation. 57% fractionation of the assemblage plagioclase (35.6%), orthopyroxene (9.7%), clinopyroxene (7.8%), ilmenite (0.6%) and magnetite (3.4%) from a plagioclase-pyroxene andesite can produce liquids of rhyolitic bulk composition. REE concentrations produced by this model are consistent with those observed in the rhyolites but predicted Ba and Rb values are lower and V concentrations are higher than those in the rhyolites. Andesite fractionation also produces an unrealistic fractionation of the Cr/V ratio.A non-modal melting model involving 35% melting of a granulitic assemblage (plagioclase + quartz + clinopyroxene + orthopyroxene + biotite + magnetite + cordierite) with a bulk composition equivalent to the Western Basement can reproduce the REE pattern of the rhyolites as well as the concentrations of Rb and Ba. Sr values remain anomalously high, but the Cr/V ratio does not indicate fractionation. Absolute values of Cr and V are within the uncertainties of published crystal—liquid partition coefficients. The rhyolites have relatively flat REE patterns (La/Yb 7.5), as do the greywackes (La/Yb 8.2), so it is therefore unlikely that the rhyolites equilibrated with a garnet or amphibole-bearing assemblage.     

Hydrothermal Mn-deposits of the Franciscan Assemblage,II. Isotope and trace element geochemistry,and implications for hydrothermal convection at spreading centers

Major element, trace element and Sr, Nd, Pb and O isotopic data for a Franciscan Mn-deposit suggest an origin by seafloor hydrothermal circulation. Based onQ-mode factor analysis the cherts and Mn-lenses of the Blue Jay mine formed from a combination of 4 components representing 1 biogenic, 1 hydrothermal, and 2 detrital sources. RbSr, UThPb and O isotopic systematics in the Mn-lenses were affected by input from the hydrothermal circulation of material leached from the underlying basalts. Nd isotopic compositions in both cherts and Mn-lenses are identical and within the range measured for Pacific Ocean water suggesting the REE were not mobilized by hydrothermal activity. Correlation of δ¹⁸O with SiO₂ and MnO₂ in the Mn-lenses implies the lenses formed by simple mixing of hydrothermally derived Mn-oxides with seawater and biogenic silica. δ¹⁸O of the cherts is both uniform and depleted relative to DSDP Jurassic cherts but similar to microquartz-bearing cherts of the Monterey Formation: this suggests that diagenetic activity exerted more control on oxygen isotope compositions then hydrothermal alteration or metamorphism. Finally, a well defined RbSr isochron of158 ± 5Myr was obtained for these cherts and opens the possibility of determining absolute radiometric ages for similar cherts throughout the geologic record.     

Carbon isotopic study of individual alcohol compounds in modern sediments from Nansha Islands sea area, China

Carbon isotopic compositions of individual n-alkanols and sterols in modern sediments from the Nansha Islands sea area are measured after derivatization to trimethylsilyl ethers by the new isotopic analytical technique of GC/C/IRMS. The effects of the three added silyl carbon atoms in every alcohol molecule on these compound isotopic compositions and the characteristics of their carbon isotopic compositions are studied. Then their biological sources are discussed using their carbon isotopic compositions. Project supported by the National Natural Science Foundation of China and Project of the Multidisciplinary Oceanographic Expedition of Chinese Academy of Sciences to Nansha Islands.