Continental recycling and true continental growth

Continental crust is very important for evolution of life because most bioessential elements are supplied from continent to ocean. In addition, the distribution of continent affects climate because continents have much higher albedo than ocean, equivalent to cloud. Conventional views suggest that continental crust is gradually growing through the geologic time and that most continental crust was formed in the Phanerozoic and late Proterozoic. However, the thermal evolution of the Earth implies that much amounts of continental crust should be formed in the early Earth. This is “Continental crust paradox”.Continental crust comprises granitoid, accretionary complex, and sedimentary and metamorphic rocks. The latter three components originate from erosion of continental crust because the accretionary and metamorphic complexes mainly consist of clastic materials. Granitoid has two components: a juvenile component through slab-melting and a recycling component by remelting of continental materials. Namely, only the juvenile component contributes to net continental growth. The remains originate from recycling of continental crust. Continental recycling has three components: intracrustal recycling, crustal reworking, and crust–mantle recycling, respectively. The estimate of continental growth is highly varied. Thermal history implied the rapid growth in the early Earth, whereas the present distribution of continental crust suggests the slow growth. The former regards continental recycling as important whereas the latter regarded as insignificant, suggesting that the variation of estimate for the continental growth is due to involvement of continental recycling.We estimated erosion rate of continental crust and calculated secular changes of continental formation and destruction to fit four conditions: present distribution of continental crust (no continental recycling), geochronology of zircons (intracontinental recycling), Hf isotope ratios of zircons (crustal reworking) and secular change of mantle temperature. The calculation suggests some important insights. (1) The distribution of continental crust around at 2.7 Ga is equivalent to the modern amounts. (2) Especially, the distribution of continental crust from 2.7 to 1.6 Ga was much larger than at present, and the sizes of the total continental crust around 2.4, 1.7, and 0.8 Ga became maximum. The distribution of continental crust has been decreasing since then. More amounts of continental crust were formed at higher mantle temperatures at 2.7, 1.9, and 0.9 Ga, and more amounts were destructed after then. As a result, the mantle overturns led to both the abrupt continental formation and destruction, and extinguished older continental crust. The timing of large distribution of continental crust apparently corresponds to the timing of icehouse periods in Precambrian.     

Another sea area separated from the Panthalassic Ocean in the Norian,the Late Triassic: The lowest Sr isotopic composition of the Ishimaki limestone in central Japan

Mt. Ishimaki is the Jurassic accretionary complex of the Chichibu Belt in Toyohashi City, near Nagoya in central Japan. The Ishimaki limestone is thought to be seamount-type limestone. The P₁ elements of the conodonts Norigondolella navicula and Ancyrogondolella quadrata found in the limestone indicate it is of Norian age. The Sr isotopic compositions of 45 Ishimaki limestone samples ranged from 0.7055 to 0.7077. Eighteen of these samples had lower Sr isotopic compositions than the lowest Sr isotopic composition (0.7068) of seawater throughout the Phanerozoic. The Sr isotopic compositions in the limestone block are generally lower at the base of the block and higher at the top. The present Sr isotopic compositions of the Ishimaki limestone are unlikely to have been reduced by post-depositional alteration because most of the limestone samples had a low amount of Mn (<300 ppm) or high Sr/Mn ratios (>2) and the conodont elements had low (1–2) CAI (conodont alteration index) values. Additionally, there was little acid-insoluble residue. Thus, the low Sr isotopic compositions are thought to represent the strontium of the past ambient seawater. The low Sr isotopic compositions are in complete disagreement with the generally recognised range of seawater Sr isotopic compositions in the Norian stage of the Late Triassic (0.7075–0.7078) because the depositional environment of the Ishimaki limestone was closed or semi-closed from the Panthalassic Ocean. Therefore, the Sr isotopic composition of the limestone differs from that of the Panthalassic seawater. The low Sr isotopic compositions were probably affected by Sr inflows from mafic oceanic crust by hydrothermal fluid circulation or from hinterlands surrounded by mafic rocks by river water circulation.     

Occurrence and chemical composition of the Eoarchean carbonate rocks of the Nulliak supracrustal rocks in the Saglek Block of northeastern Labrador,Canada

The Eoarchean Nulliak supracrustal rocks in the Saglek Block of northeastern Labrador, Canada, contain some of the world's oldest carbonate rocks. This work attempted to reveal the origin of the carbonate rocks and estimate the surface environmental conditions of the early Earth based on their occurrence and geochemistry. They occur together with mafic and ultramafic rocks in Pangertok Inlet and St. John's Harbour South, whereas they are interlayered with pelitic rock layers with quartzofeldspathic mineral assemblages in St. John's Harbour East and Big Island. The geological occurrence suggests that the formers were formed around hydrothermal fields, whereas the latters were deposited near a continental margin. Some carbonate rocks have high SiO₂, Al₂O₃, and Zr contents, indicating that the silicification and involvement of detrital materials influenced their composition; thus, pure carbonate rocks were selected using a combined filter of the SiO₂, TiO_2, Al₂O₃, Zr, and Ba contents. The selected carbonate rocks have positive La, Eu, Gd, Y, U, Pb, and Sr anomalies, negative Nb, Zr, and Hf anomalies, and relatively small enrichment in heavy rare earth elements (HREEs). The La and Y anomalies suggest that they originated from chemical sediments precipitated from seawater. On the other hand, the small HREE-enrichment suggests that REEs were mainly dissolved as REE-carbonate complexes in seawater or that the riverine influxes were dominated by the detritus of Eoarchean continental crusts, presumably composed of HREE-depleted TTG. The U anomaly suggests that uranium was more dissolved than Th as U-bearing carbonate complexes in seawater. The Nulliak carbonate rocks also show a positive correlation between Y and Eu anomaly values, suggesting that the precipitation of iron-oxyhydroxide causing the Y anomaly was more significant near the hydrothermal fields than the continental margin, consistent with an alkaline hydrothermal model.     

Geochemistry and petrogenesis of carbonatites from South Nam Xe,Lai Chau area,northwest Vietnam

This paper presents a study of the petrography, mineral chemistry, geochemistry, and Sr–Nd–Pb–C–O isotope systematics of carbonatite dykes and associated rocks from the northeastern part of the Song Da intracontinental rift in South Nam Xe (northwest Vietnam) aimed at constraining the origin of the carbonatite magmas. The carbonatites are characterized by SiO₂ < 12.18 wt.% and by wide ranges in FeO, MgO and CaO content that define them as calciocarbonatite and ferrocarbonatite. On U–Th–Pb isochron diagrams, whole rocks and mineral separates from the ferrocarbonatites form linear arrays corresponding to ages of 30.2–31.6 Ma (Rupelian, Oligocene). The South Nam Xe carbonatites are extremely enriched in Sr, Ba, and light rare earth elements (LREE), and depleted in high field strength elements (HFSE) (e.g. Ti, Nb, Ta, Zr and Hf). The age–corrected Sr–Nd–Pb isotope ratios and C isotope data are relatively uniform (⁸⁷Sr/⁸⁶Sr_(t) = 0.708193–0.708349; ¹⁴³Nd/¹⁴⁴Nd_(t) = 0.512250–0.512267; ε_Nd(t) = ?6.46 to ?6.80; ²⁰⁶Pb/²⁰⁴Pb_(t) = 18.26–18.79; ²⁰⁷Pb/²⁰⁴Pb_(t) = 15.62–15.64; ²⁰⁸Pb/²⁰⁴Pb_(t) = 38.80–39.38; δ¹³C_V-PDB = –2.7?‰ to ?4.1?‰). These isotopic compositions indicate source contamination that occurred before the production of the carbonatite magmas, and did not change noticeably during or after emplacement. The variation in oxygen isotopes is consistent with the change in mineral compositions and trace element abundances: the lower δ¹⁸O values (9.1–11.0?‰) coupled with Sr-rich, Mn-poor calcite, and igneous textures such as triple junctions among calcite grain boundaries, define a magmatic origin. However, the elevated δ¹⁸O values of the ferrocarbonatites (12.0–13.3?‰) coupled with a volatile-bearing mineral assemblages (including REE fluorcarbonates, sulfates, sulfides and fluorite) may be due to interaction with meteoric water during low-temperature alteration. High δ¹³C values and Sr–Pb ratios, and low Rb/Sr (0.00014–0.00301), Sm/Nd (0.089–0.141) and ¹⁴³Nd/¹⁴⁴Nd ratios, coupled with very high Sr-Nd concentrations, suggest the involvement of an enriched mantle component, which probably resulted from metasomatism due to the migration of subducted material. Because of the lack of tectonic data and the limited number of samples studied, this conclusion is still ambiguous and requires further study.     

EXPERIMENTAL STUDIES ON BEHAVIORS OF MAJOR AND MINOR LITHOPHILE ELEMENTS IN VAPORIZATION UNDER EVACUATED CONDITION

In order to investigate the volatilities of major and minor lithophile elements, evaporation experiments by electron bombardment were carried out employing basaltic rock powder. The elements studied included Al, Fe, Ca, Mg, Mn, Na, K, Rb, Ba and REE. The source crucible was heated to about 2300 °K, and the vaporized material was collected at different distances from the source. The enrichment factors of studied elements in the material collected on the condensation plate were calculated relative to the starting material. Patterns of REE removed during flights between varying distances were also evaluated.     

Detrital zircon evidence for Hf isotopic evolution of granitoid crust and continental growth

We have determined U-Pb ages, trace element abundances and Hf isotopic compositions of approximately 1000 detrital zircon grains from the Mississippi, Congo, Yangtze and Amazon Rivers. The U-Pb isotopic data reveal the lack of >3.3 Ga zircons in the river sands, and distinct peaks at 2.7-2.5, 2.2-1.9, 1.7-1.6, 1.2-1.0, 0.9-0.4, and <0.3 Ga in the accumulated age distribution. These peaks correspond well with the timing of supercontinent assembly. The Hf isotopic data indicate that many zircons, even those having Archean U-Pb ages, crystallized from magmas involving an older crustal component, suggesting that granitoid magmatism has been the primary agent of differentiation of the continental crust since the Archean era. We calculated Hf isotopic model ages for the zircons to estimate the mean mantle-extraction ages of their source materials. The oldest zircon Hf model ages of about 3.7 Ga for the river sands suggest that some crust generation had taken place by 3.7 Ga, and that it was subsequently reworked into <3.3 Ga granitoid continental crust. The accumulated model age distribution shows peaks at 3.3-3.0, 2.9-2.4, and 2.0-0.9 Ga.The striking attribute of our new data set is the non-uniformitarian secular change in Hf isotopes of granitoid crusts; Hf isotopic compositions of granitoid crusts deviate from the mantle evolution line from about 3.3 to 2.0 Ga, the deviation declines between 2.0 and 1.3 Ga and again increases afterwards. Consideration of mantle-crust mixing models for granitoid genesis suggests that the noted isotopic trends are best explained if the rate of crust generation globally increased in two stages at around (or before) 3.3 and 1.3 Ga, whereas crustal differentiation was important in the evolution of the continental crust at 2.3-2.2 Ga and after 0.6 Ga. Reconciling the isotopic secular change in granitoid crust with that in sedimentary rocks suggests that sedimentary recycling has essentially taken place in continental settings rather than active margin settings and that the sedimentary mass significantly grew through addition of first-cycle sediments from young igneous basements, until after ∼1.3 Ga when sedimentary recycling became the dominant feature of sedimentary evolution. These findings, coupled with the lack of zircons older than 3.3 Ga in river sands, imply the emergence of large-scale continents at about 3.3 Ga with further rapid growth at around 1.3 Ga. This resulted in the major growth of the sedimentary mass between 3.3 and 1.3 Ga and the predominance of its cannibalistic recycling later.     

Grain-scale iron isotopic distribution of pyrite from Precambrian shallow marine carbonate revealed by a femtosecond laser ablation multicollector ICP-MS technique: Possible proxy for the redox state of ancient seawater

The redox state of Precambrian shallow seas has been linked with material cycle and evolution of the photosynthesis-based ecosystem. Iron is a redox-sensitive element and exists as a soluble Fe(II) species or insoluble Fe(III) species on Earth’s surface. Previous studies have shown that the iron isotopic ratio of marine sedimentary minerals is useful for understanding the ocean redox state, although the redox state of the Archean shallow sea is poorly known. This is partly because the conventional bulk isotope analytical technique has often been used, wherein the iron isotopic record may be dampened by the presence of isotopically different iron-bearing minerals within the same sample. Here we report a microscale iron isotopic ratio of individual pyrite grains in shallow marine stromatolitic carbonates over geological time using a newly developed, near-infrared femtosecond laser ablation multicollector ICP-MS technique (NIR-fs-LA-MC-ICP-MS).We have determined that the grain-scale iron isotopic distribution of pyrite from coeval samples shows a bimodal (2.7 and 2.3 Ga) or unimodal pattern (2.9, 2.6, and 0.7 Ga). In particular, pyrite from the 2.7 Ga Fortescue Group shows a unique bimodal distribution with highly positive (+1.0‰ defined as Type 1) and negative δ⁵⁶Fe values (−1.8‰ defined as Type 2). Type 1 and 2 pyrites occasionally occur within different siliceous layers in the same rock specimen. Layer-scale iron isotopic heterogeneity indicates that the iron isotopic ratios of the two types of pyrite are not homogenized by diagenesis after deposition. Some cubic pyrites have a core with a positive δ⁵⁶Fe value (1‰) and a rim with a crustal δ⁵⁶Fe value (0‰). The observed isotopic zoning suggests that the positive δ⁵⁶Fe value is a primary signature at the time of stromatolite formation, while secondary pyrite precipitated during diagenesis.The positive δ⁵⁶Fe value of Type 1 and the large iron isotopic difference between Type 1 and 2 (2.8‰.) suggest partial Fe(II) oxidation in the 2.7-Ga shallow sea, i.e., pyritization of ⁵⁶Fe-enriched ferric oxyhydroxide (Type 1) and ⁵⁶Fe depleted Fe²⁺aq in seawater (Type 2). Type 2 pyrite was probably not produced by microbial iron redox cycling during diagenesis because this scenario requires a higher abundance of pyrite with δ⁵⁶Fe of 0‰ than of −1.8‰. Consequently, the degree of Fe(II) oxidation in the 2.7-Ga shallow sea can be estimated by a Fe²⁺aq steady-state model. The model calculation shows that half the Fe²⁺aq influx was oxidized in the seawater. This implies that O₂ produced by photosynthesis would have been completely consumed by oxidation of the Fe²⁺aq influx. Grain-scale iron isotopic distribution of pyrite could be a useful index for reconstructing the redox state of the Archean shallow sea.     

Responses of Estuarine Bacterioplankton,Phytoplankton and Zooplankton to Dissolved Organic Carbon (DOC) and Inorganic Nutrient Additions

The response of planktonic bacteria and phytoplankton to various additions of dissolved organic carbon (DOC) as glucose, with and without inorganic nutrients (nitrogen and phosphorus), was tested in the upper to mid Hunter Estuary, Australia. In situ microcosms (1.25 L) were performed at two sites with varying salinities over three seasons. Analysis of variance showed a significant difference among control and treatments for all seasons for the bacterial, dissolved oxygen and chlorophyll a responses (P < 0.05). A significant interaction between treatment and site was found in autumn for dissolved oxygen, autumn and spring for bacterial and spring for chlorophyll a responses. At both sites for each season, and on nearly all occasions, bacterial surface area was enhanced by DOC addition as indicated by both increased bacterial abundance and dissolved oxygen utilisation. DOC in combination with inorganic nutrients sometimes further enhanced the bacterial response compared to DOC alone. Inorganic nutrients alone did not enhance growth of the heterotrophic bacterioplankton. Addition of DOC alone led to decreased chlorophyll a relative to the control, probably due to competition for limited inorganic nutrients with the bacterioplankton DOC non-limiting conditions. Results suggest that the heterotrophic community was limited by DOC at both sites and across seasons. An experiment with a larger volume (70 L), performed over a longer time, compared a control with DOC addition. Increased bacterial biomass as a result of DOC addition occurred at day 2. Chlorophyll a did not significantly differ between treatments. An increase in zooplankton density was recorded in the DOC treatment relative to the control at day 10. This study supports the contention that increased DOC delivery with river inflows through environmental flow allocations will stimulate heterotrophic bacterioplankton production in the upper Hunter Estuary.     

Zircon U–Pb ages from tuff beds of the upper Mesozoic Tetori Group in the Shokawa district,Gifu Prefecture,central Japan†

Abstract The upper Mesozoic Tetori Group contains numerous fossils of plants and marine and non‐marine animals. The group has the potential to provide key information to improve our understanding of the Middle Jurassic to Early Cretaceous biota of East Asia. However, the depositional age of the Tetori Group remains uncertain, and without good age constraints, accurate correlation with other areas is very difficult. As a first step in obtaining reliable ages for the formations within the Tetori Group, we used laser ablation‐inductively coupled plasma–mass spectrometry to measure the U–Pb ages of zircons collected from tuff beds in the Shokawa district, Takayama City, Gifu Prefecture, central Japan. The youngest reliable U–Pb ages from the tuff beds of the Ushimaru, Mitarai and Okurodani Formations are 130.2 ± 1.7, 129.8 ± 1.0 and 117.5 ± 0.7 Ma, respectively (errors represent 2 SE). These results indicate that the entire Tetori Group in the Shokawa district, which was previously believed to be correlated to the Upper Jurassic to Lower Cretaceous, is in fact correlated to the Lower Cretaceous. The maximum ages of the Ushimaru, Mitarai and Okurodani Formations are late Hauterivian to Barremian, late Hauterivian to Barremian and Barremian to Aptian, respectively.     

Application of distinct element analysis to three simple block models aimed at practical application to toppling failure of fissured rock slopes

To examine the accuracy and the chracteristics of the Distinct Element Method (DEM) which has non-deformable elements, the results simulated by the DEM were compared to the results of experiments and/or theories for three simple block models of a pillar, a mass and a toppling model. Consequently, it was elucidated that the DEM is a good numerical method which can be effectively applied to toppling failure of real fissured rock slopes.