Lead isotopes in island arcs

New lead isotope data for calc-alkaline volcanic rocks from New Zealand and the Lesser Antilles, combined with published data for Japan and the Andes, show that the spread of isotopic composition in each volcanic arc region is small (2–4% range in Pb206/Pb204) compared to the range of values observed (8%). Pb207 and Pb206 increase systematically from Japan to the Andes to New Zealand to the Caribbean. Likewise Pb208 and Pb206 are positively correlated, but there is evidence of long term (10⁸ m.y.) differences of Th/U between the regions studied. The apparent U/Pb ratios of Peruvian, New Zealand and Caribbean calc-alkaline volcanics do not differ greatly from the apparent ratio for the single stage growth curve for stratiform Pb ores. In contrast the apparent U/Pb ratios for Japanese calc-alkaline volcanics are distinctly lower. Although the Japanese Pb has model ages near zero, the other volcanic arcs have negative (future) model ages, the Caribbean samples being most extreme in this respect. Published oceanic volcanic and sediment lead isotopic composition data and the new results are consistent with a model of volcanic arc evolution in which oceanic sediments are dragged into the mantle, mixed to some degree with mantle material, and partially melted to form calc-alkaline magmas. Either constant continental volume or continental growth are compatible with this process. The mixing of two separate « frequently mixed » leads is the minimum complexity required to explain volcanic are leads. Mathematically there are probably no single-stage leads but isotopic homogenization during earth history has caused lead isotopes to closely approximate a single stage growth. The use of lead isotopic composition as a « tracer » suggests that mantle — crust geochemical evolution involves an exchange of material and is not simply a one-way process. The Pb isotopic composition of the Auckland, New Zealand alkali basalts is apparently the result of incomplete mixing of two leads to give a linear array of Pb207/Pb204-Pb206/Pb204 data with negative slope.     

Concentrations of trace elements in muscle of sturgeons in the Caspian Sea

Concentrations of 21 trace elements were determined in muscle of beluga (Huso huso), Persian sturgeon (Acipenser persicus), Russian sturgeon (Acipenser gueldenstaedtii), ship sturgeon (Acipenser nudiventris) and stellate sturgeon (Acipenser stellatus) collected from coastal regions of Azerbaijan, Iran, Kazakhstan and Turkmenistan, surrounding the Caspian Sea during 2000-2001. Concentrations of Mn, Co, Cu, Mo, Sn, Hg, Pb and Bi in the muscle were apparently different among the five species of sturgeons. Especially, beluga showed the highest concentrations of Hg, Pb and Mn in all the five species. In addition, more than half of the individuals of beluga exceeded the guideline level (0.3 microg/g wet wt.) of Hg for food in UK. However, V, Cr, Zn, Ga, Rb, Sr and Ba concentrations were similar among five sturgeons. Growth-dependent increase in Hg in beluga, Cu in Persian sturgeon, and Zn in Russian sturgeon were observed, whereas V, Mn, Co, Cu, Ga, Sr, Mo, Sn, Hg and Bi concentrations in Persian sturgeon, Pb in ship sturgeon, and Cr, Mn, and Rb in stellate sturgeon were negatively correlated with body length. All species of sturgeon in Azerbaijan showed the highest concentration of Sr and the lowest concentration of Rb, while the five sturgeons from Iran showed opposite trends. Concentration of V, which is present in oil, in sturgeons in the Caspian Sea was considerably lower than that of fish from Kuwait, but was comparable to that of Cambodia and the Gulf and Gulf of Oman. To our knowledge, this study provides the first extensive data on multielemental accumulation in sturgeons of the Caspian Sea.     

Lead isotopes in Archaean Plutonic rocks

Archaean intrusive rocks have initial Pb isotopic compositions which show a varied and complex history for the source regions of the rocks. Even the oldest rocks from Greenland indicate heterogeneous U and Pb distribution prior to 3800 m.y. ago. Source regions with μ values less than 7 must have played a significant role in the early history of the earth. By late Archaean time U/Pb ratios of source regions had increased substantially. Data from Australia and North America show distinct regional differences, both within and between continents.     

Lead isotopes and age of Hawaiian lherzolite nodules

The reaction between enstatite (En_95.3Fs_4.7) and CaCO₃ has been studied at pressures between 23 and 77 kbars and at temperatures between 800° and 1400°C. At 1000°C enstatite and CaCO₃ react to form dolomite and diopside solid solutions at pressures below approximately 45 kbars and magnesite and diopside solid solutions at higher pressures. The curve for the reaction dolomite_ss + enstatite_ss ? magnesite_ss + diopside_ss lies between 40 to 45 kbars at 1000°C and between 45 and 50 kbars at 1200°C. It is very close to the graphite-diamond transition curve. These experimental results indicate that calcite (or aragonite) is unstable in the presence of enstatite, and that dolomite and magnesite are the stable carbonates at high pressures. The forsterite + aragonite assemblage is, however, stable to at least 80 kbars at 800°C. It is suggested that in the upper mantle where enstatite is present, dolomite is stable to depths of about 150 km and magnesite is stable at greater depths in the continental regions, assuming that the partial pressure of CO₂ is equal or close to the total pressure. It is also suggested that carbonate inclusions in pyroxene can be used as an indicator of the depth of their equilibration; dolomite inclusions in enstatite would be formed at depths shallower than 150 km and magnesite inclusions in diopside at greater depths. Eclogite and peridotite inclusions in kimberlite may be classified on this basis.     

Lead concentrations and isotopes in aerosols from Xiamen, China

To investigate the magnitude and origin of lead (Pb) pollution in the atmosphere of Xiamen, China, 40 aerosol samples were collected from the coast of Xiamen from January to December 2003. All these samples were measured for Pb isotopic compositions (²⁰⁸Pb/²⁰⁶Pb = 2.10897 ± 0.00297, ²⁰⁷Pb/²⁰⁶Pb = 0.85767 ± 0.00159, n = 40) using a Multi-collector-Inductively Coupled Plasma Mass Spectrometer (MC-ICPMS). Thirty-five out of forty samples were also measured for Pb concentrations (79.1 ± 38.3 ng/m³, n = 35) by Atomic Absorption Spectroscopy (AAS). The results indicate that the Pb concentrations display significant seasonal variations while Pb isotopic ratios remain relatively constant. The Pb concentrations were high in January and February, abruptly decreased in March, remained relatively constant (but low) from April to August, and then gradually increased from September to December. This corresponds to the rainless climate in winter and rain scavenging in summer. The higher Pb concentration of Xiamen aerosols in winter and spring may be also caused by long-range transferred anthropogenic Pb during the northeastern monsoon seasons. Although the use of leaded gasoline in Xiamen was banned in 2000, our new data indicate that the Pb annual concentrations of aerosols in Xiamen increased about 12% when compared to the data measured between 1991 and 1993. Thus, Pb pollution in the atmosphere of Xiamen has not receded even after the phase-out of leaded gasoline. Our results further confirm the previous studies’ conclusion that the primary source of atmospheric Pb in China, especially in South China, is the vast combustion of lead-containing coal, not leaded gasoline.     

A comparative study of boron isotopes and trace elements of the marine foraminifers during the last glacial maximum and Holocene

Boron isotopic compositions in marine planktonic foraminifers can record changes in seawater pH and hence provide a new tool to reconstruct the changes of paleo-atmospheric PCO2.Here a comparative study was done on boron isotopes and trace element abundances of planktonic foraminifers,Globigerinoides sacculifer and Globigerinoides ruber from three tropical ODP sites,Site 806B,Site 664C and Site 999A.It is demonstrated here that G.ruber is a better species to be used for downcore boron isotope analyses on gl...     

Variations in trace elements,isotopes, and organic geochemistry during the Hangenberg Crisis,Devonian–Carboniferous transition,northeastern Vietnam

The Hangenberg Crisis at the Devonian–Carboniferous boundary is known as a polyphase extinction event that affected more than 45 % of marine and terrestrial genera. As the cause of this event is still debated, analyses were carried out on sedimentary samples from the Devonian–Carboniferous Pho Han Formation in northeastern Vietnam to reconstruct the paleoenvironment around the time of this event using stable carbon isotopes; total sulfur; manganese; vanadium; molybdenum; and sedimentary organic matter, such as dibenzothiophenes, cadalene, and regular steranes. These geochemical signatures provide a high‐resolution redox history for this section and show that transgression‐driven high primary productivity, possibly enhanced by terrestrial input, caused severe oxygen depletion along the continental margin of the South China block during the Hangenberg Crisis.     

Distribution of trace elements in spinel and garnet peridotites

The distribution of trace elements in the upper mantle has been discussed on the basis of the trace element abundances in bulk rocks and constituent minerals of two spinel and garnet facies peridotite xenoliths in alkali basalts from eastern China. The data presented are consistent with the suggestion that highly incompatible elements (Rb, Ba, Th, U, Sr, Nb, Ta) mainly reside in intergranular components, and to a lesser extent in fluid inclusions in minerals. The LILE composition in olivine and orthopyroxene can be seriously affected by the presence of fluid inclusions. Consequently the subsolidus partitioning of the LILE cannot be used to infer the olivine-melt and orthopyroxene-melt partition coefficients for these elements. There is a significant difference in (Opx/Cpx)_HREE ratios for spinel and garnet peridotites, suggesting a P-T control on equilibrium partition coefficients.     

Meteoritic and non-meteoritic trace elements in Luna 16 samples

Two Luna 16 soils have been analyzed for Ag, Au, Bi, Br, Cd, Co, Cs, Cu, Ga, Ge, In, Ur, Ni, Rb, Re, Sb, Se, Te, Tl, and Zn. A meteoritic component similar to that in Apollo 11 and 12 soils seems to be present, corresponding to ∼1.5 to 2% Cl chondrites or equivalent. It probably consists largely of micrometeorites. Three elements show strong enrichments compared to Apollo 11 and 12 soils: Cd (5× to 200×), Ag (5× to 10×), and Bi (3×). Presumably these elements were brought in by Cd-Ag-Bi rich material, similar to that in Unit VI of Apollo core 12028.     

Lead and strontium isotopes in Cretaceous kimberlites and mantle-derived xenoliths from Southern Africa

Concentrations of lead, uranium and thorium and isotopic compositions of lead are reported for twelve Cretaceous kimberlites and five Cretaceous nucleated autoliths. The samples are from Lesotho and from the area around Kimberley (Cape Province, South Africa). In the case of the autoliths potassium, rubidium and strontium concentrations and⁸⁷Sr/⁸⁶Sr ratios were also measured.Work reported on clinopyroxenes from mantle-derived xenoliths in kimberlites includes lead isotopes for twelve samples and strontium isotopes for nine of these.The autoliths have initial⁸⁷Sr/⁸⁶Sr ratios between 0.7035 and 0.7095. A large spread in initial lead isotope ratios (²⁰⁶Pb/²⁰⁴Pb: 17.6–20;²⁰⁸Pb/²⁰⁴Pb: 37.7–39.5) was found in the matrix kimberlites and autoliths. In the²⁰⁷Pb/²⁰⁴Pb vs.²⁰⁶Pb/²⁰⁴Pb plot, the initial lead isotope ratios of the kimberlite and autolith samples roughly define a slope of 0.10, corresponding to an age of 1575 m.y. With respect to the spread of initial ratios as well as with respect to this slope, the kimberlite and autolith lead isotopic pattern is comparable to patterns obtained from carbonatites and ocean island volcanics.The xenoliths studied include coarse-granular and porphyroclastic material from the Kimberley area and coarse-granular samples from Lesotho. Their⁸⁷Sr/⁸⁶Sr ratios are generally between 0.704 and 0.706 but a value of 0.713 was found in one sample. They show a surprisingly large spread in lead isotope ratios (²⁰⁶Pb/²⁰⁴Pb: 17.5–20;²⁰⁸Pb/²⁰⁴Pb: 37.3–39.4).The isotopic patterns of the xenolithic material and of the kimberlites and autoliths are considered to provide a strong indication that the upper mantle beneath Southern Africa is isotopically heterogeneous on a regional scale.     

A record of Miocene carbon excursions in the South China Sea

High-resolution δ¹³C records are presented for the Miocene benthic foraminifersCibicidoides wuellerstorfi andC. kullenbergi (24-5 Ma) and the planktonic foraminiferGlobigerinoides sacculifer (18-5 Ma) from ODP Site 1148A (18° 50.17’N, 116° 33.93’E, water depth 3308.3 m), northern South China Sea. The general pattern of parallel benthic and planktonic δ¹³C shows a decrease trend of δ¹³C values from the early-middle Miocene to the middle-late Miocene. Two distinct δ¹³C positive excursions at 23.1-22.2 and 17.3-13.6 Ma, and two negative excursions at 10.2-9.4 and 6.9-6.2 Ma have been recognized. All these events are cosmopolitan, providing the good data for the stratigraphic correlation of the South China Sea with the global oceans as well as for studying the changes of the global carbon reservoir and its corresponding climate.     

Rare earth and other trace elements in historic azorean lavas

Rare earth element (REE) and other trace element compositions of 16 lavas from all historic and 2 prehistoric eruptions on 5 islands of the Azores Archipelago show notable intra-and inter-island differences. Fe enrichment and “compatible” element depletion due to fractional crystallization have been superimposed on variations established in the source area. Fractionation of La/Sm, U/Th, K/Na and “large ion lithophile” (LIL) element abundances are probably related to variable fusion of a source peridotite whose LIL element distribution cannot be exactly specified in view of its possible heterogeneity. Relative light-REE enrichment in basalt appears greatest on the “potassic” island São Miguel, the more sodic island Fayal and one lava from Pico, and least in basalts from the “sodic” islands Terceira, São Jorge and Pico. This variation is matched by most other LIL elements, although P shows unexpected enrichment in Terceira lavas, otherwise the least LIL element-enriched and most heavy-REE-enriched. Upper mantle phase chemistry is probably critical in establishing the patterns. In particular, P—REE covariance may reflect phase stabilities of apatite and (P-bearing) garnet in the upper mantle. Distribution patterns of REE in the historic lavas are similar to those of basalts from the Atlantic median rift at the crest of the Azores “platform”. Transition to light-REE-depleted rift-erupted basalts to the southwest is believed to be step-wise with increasing water depth, possibly indicating retention of a light-REE-rich phase in the residue from partial fusion as intersection of geotherm and peridotite solidus occur at lower pressures. The source mantle for the Azores basalts is probably light-REE- and LIL element-enriched but we find no evidence so far to suggest its emplacement by thermal “plume” activity.     

Shifting environmental baselines in the Red Sea

The Red Sea is among the world’s top marine biodiversity hotspots. We re-examined coastal ecosystems at sites surveyed during the 1980s using the same methodology. Coral cover increased significantly towards the north, mirroring the reverse pattern for mangroves and other sedimentary ecosystems. Latitudinal patterns are broadly consistent across both surveys and with results from independent studies. Coral cover showed greatest change, declining significantly from a median score of 4 (1000–9999 m²) to 2 (10–99 m²) per quadrat in 2010/11. This may partly reflect impact from coastal construction, which was evident at 40% of sites and has significantly increased in magnitude over 30 years. Beach oil has significantly declined, but shore debris has increased significantly. Although substantial, levels are lower than at some remote ocean atolls. While earlier reports have suggested that the Red Sea is generally healthy, shifting environmental baselines are evident from the current study.     

Carbon isotopes,sulfur isotopes,and trace elements of the dolomites from the Dengying Formation in Zhenba area,southern Shaanxi: Implications for shallow water redox conditions during the terminal Ediacaran

Carbon isotope, sulfur isotope, and trace element(including Rare Earth Elements, REE) analyses were conducted on the carbonates of the Dengying Formation at Lianghekou section in southern Shaanxi to reconstruct the terminal Ediacaran shallow-water environment on the northwestern margin of the Yangtze Platform. At Lianghekou section, samples in the middle 50-m of the Beiwan Member show characteristics of low ΣREE concentrations, no MREE-enriched REE distribution patterns, high Ce/Ce* values close to 1, and enriched redox-sensitive elements, whereas samples in the lower 30-m and upper 10-m show opposite characteristics of high ∑REE concentrations, MREE-enriched REE distribution patterns, low Ce/Ce* values around 0.6, and no redox-sensitive elements enriched, indicating that oxygenation did occur in the shallow water on the northwestern margin of the Yangtze Platform and redox conditions of the shallow water fluctuated from relatively oxygenated to anoxic and then back to oxygenated again. We propose that the anoxia appeared in middle of the Beiwan time may associate with the anoxic upwelled water. On one hand, abundant nutrients were brought in by this upwelling event, which stimulated the photosynthetic carbon fixation and increased the organic carbon burial under this anoxic condition, causing a peak of 3.6‰ in δ 13 C. On the other hand, because the anoxic upwelled water replaced the oxic shallow water, together with the increasing organic matter in the water column, bacterial sulfate reduction was enhanced and therefore quickly reduced the sulfate concentration, which eventually caused δ 34 S increasing to 50‰. However, as the upwelling gradually disappeared, δ 13 C and δ 34 SCAS values decreased as well in the late Beiwan time, indicating the shallow water went back to suboxic or oxic again.     

Ecological risk assessment using trace elements from surface sediments of Izmit Bay (Northeastern Marmara Sea) Turkey

The aim of this study was to study ecological risk assessment of trace elements (As, Cd, Cr, Cu, Ni, Pb and Zn) in Izmit Bay surface sediments in the <63 microm fraction. Sediment samples were collected from 8 sites along the north coastline of the bay. Samples were subjected to a total digestion technique and analyzed for major (organic carbon) and minor (As, Cd, Cr, Cu, Ni, Pb and Zn) elements. Sediments heavily contaminated are evaluated by the Sediment Quality Guidelines (SQG) of US EPA. The degree of contamination (Cd) is estimated as very high at each site. Two sets of SQGs, effect range-low/effect range median values and TEL/probable effect level (PEL) values were used in our study. Sediments from the each site are judged toxic when two or more of the PEL values exceed EPA guidelines. Our results are in agreement with previously reported sediment toxicity test results.     

Distribution and ecological risk assessment of some heavy metals in coastal surface sediments along the Red Sea,Egypt

The ecological risk assessment for Al,Zn,Cu,Ni,V,Pb,Cd,and Hg in surface sediment collected from the Egyptian Red Sea coast was evaluated using the Geo-accumulation Index(I_(geo)).Sediment Enrichment Factor(SEF) and Potential Ecological Risk Index(PERI) methods.The predominant heavy metal,aluminum,showed high concentrations along both of Aqaba Gulf(4378.8 ± 2554.1 μg/g) and southern part of the Red Sea(2972.8 + 1527.5 μg/g).while it recorded the lowest concentration in Suez Gulf(829.7 ± 398.2 μg/g).The determined heavy metal concentrations had the order of Al Zn -Ni V Pb Cu Cd Hg.The statistical analyses showed some correlations among the heavy metals contents.Several international sediment quality guidelines were used to estimate the quality of the collected sediments.Interestingly,the recorded average heavy metals concentrations were lower than those of the permissible contents for sediment quality guidelines.The Geo-accumulation index calculations(I_(geo)) proved that the investigated region could be classified as an unpolluted area.Sediment Enrichment Factor(K_(SEF)) study showed high values in Suez Gulf region.The single pollution index analysis of heavy metals in the sediments(C~i_f) indicated that Al,Zn,V,and Pb were of natural origin,while Ni,Cd and Hg were seriously affected by human activities.Interestingly,amongst,all the determined heavy metals,Cd and Hg gave moderate ecological risk indicators.     

Helium isotopes in some historical lavas from Mount Vesuvius

³He/⁴He ratios in lavas erupted during the last 360 years at Mt. Vesuvius are between 2.2 and 2.7 R_A (R_A = atmospheric ratio of 1.39 × 10⁻⁶), and are among the lowest values measured in young volcanic rocks. They are also identical to values measured in summit crater fumaroles sampled during 1987–1991. This agreement indicates that the ³He/⁴He ratio in the crater fumaroles faithfully tracks the magmatic value. The relatively low and uniform ³He/⁴He ratio in the lavas reflects either a mantle source enriched in (U + Th)/³He, or a mixture of magmatic and crustal components.