Recent macroids on the Kikai‐jima shelf,Central Ryukyu Islands,Japan

Sandy and gravelly carbonate sediments found off Kikai‐jima, southern Japan, a coral reef‐related island shelf, represent the northernmost sub‐tropical, carbonate deposits in the Central Ryukyu Islands (Ryukyus). On the Kikai‐jima shelf, at water depths of 61 to 105 m, these sediments are characterized by macroid pavements. Since the abundance of very small and of exceptionally large macroids may indicate specific hydrodynamic controls regarding constraints on growth and taphonomy, the detailed analysis of recent and fossil macroid pavements is meaningful ecologically and environmentally. Macroids, ranging in size from ca 25 to 130 mm in diameter, are spheroidal and sub‐spheroidal in shape and consist mainly of the encrusting foraminifer Acervulina inhaerens and subordinate thin encrusting and lumpy coralline algae. Accessory components include bryozoans, serpulids and, to a lesser extent, encrusting arborescent foraminifera (Homotrema and Miniacina). Low sedimentation rates and occasional movement due to current action are indicated by sizes, shapes and growth‐forms of the studied macroids, the Entobia–Gastrochaenolites–Trypanites–Maeandropolydora ichnocoenosis and the ‘Bioerosion Index’ for coated grains (introduced herein). The deep‐water tidally induced current energy was sufficient to maintain multi‐directional growth (spheroidal shapes) of the larger macroids and to initiate macroid growth using the diverse biogenic remnants as nuclei. The asymmetrical inner arrangement suggests possible periods of stability for the macroids. The residence time of the coated grain in its original environment determines the size and morphology of the macroid and the selection of coating organisms. The composition of the coating community is mainly a consequence of component growth rates in relation to turnover time and residence time. Long‐term studies are needed to assess the spatial and temporal resolution of present‐day encrusting communities across biogeographic provinces and shelf to slope regions.     

In Situ Determination of Au and Cu in Natural Pyrite by Near‐Infrared Femtosecond Laser Ablation‐Inductively Coupled Plasma‐Quadrupole Mass Spectrometry: No Evidence for Matrix Effects

Gold and copper concentrations were determined in natural pyrite by near‐infrared femtosecond LA‐ICP‐QMS, using both sulfide reference materials (pyrrhotite Po‐726 and in‐house natural chalcopyrite Cpy‐RM) and NIST SRM 610 as external calibrators. Firstly, using NIST SRM 610 as the external calibrator, we calculated the Au concentration in Po‐726 and the Cu concentration in Cpy‐RM. The calculated concentration averages for Au and Cu were similar to the values published for Po‐726 and Cpy‐RM, respectively. Secondly, we calculated Au and Cu concentrations taking NIST SRM 610 as an unknown sample and using Po‐726 and Cpy‐RM as external calibrators. Again, the average values obtained closely reflected the preferred concentrations for NIST SRM 610. Finally, we calculated Au and Cu concentrations in natural pyrite using sulfide and silicate reference materials as external calibrators. In both cases, calculated concentrations were very similar, independent of the external calibrator used. The aforementioned data, plus the fact that we obtained very small differences in relative sensitivity values (percentage differences are between 5% and 17% for ⁵⁷Fe, ⁶³Cu and ¹⁹⁷Au) on analyses of silicate and sulfide RMs, indicate that there were no matrix effects related to the differences in material composition. Thus, it is possible to determine Au and Cu in natural sulfides using NIST silicate glasses as an external calibrator.     

Palaeoenvironmental significance of Late Permian palaeosols in the South‐Eastern Iberian Ranges,Spain

The Late Permian (Wuchiapingian) Alcotas Formation in the SE Iberian Ranges consists of one red alluvial succession where abundant soil profiles developed. Detailed petrographical and sedimentological studies in seven sections of the Alcotas Formation allow six different types of palaeosols, with distinctive characteristics and different palaeogeographical distribution, to be distinguished throughout the South‐eastern Iberian Basin. These characteristics are, in turn, related to topographic, climatic and tectonic controls. The vertical distribution of the palaeosols is used to differentiate the formation in three parts from bottom to top showing both drastic and gradual vertical upwards palaeoenvironmental changes in the sections. Reconstruction of palaeoenvironmental conditions based on palaeosols provides evidence for understanding the events that occurred during the Late Permian, some few millions of years before the well‐known Permian‐Triassic global crisis.     

Rare Earth Deposits of North America

Rare earth elements (REE) have been mined in North America since 1885, when placer monazite was produced in the southeast USA. Since the 1960s, however, most North American REE have come from a carbonatite deposit at Mountain Pass, California, and most of the world’s REE came from this source between 1965 and 1995. After 1998, Mountain Pass REE sales declined substantially due to competition from China and to environmental constraints. REE are presently not mined at Mountain Pass, and shipments were made from stockpiles in recent years. Chevron Mining, however, restarted extraction of selected REE at Mountain Pass in 2007. In 1987, Mountain Pass reserves were calculated at 29 Mt of ore with 8.9% rare earth oxide based on a 5% cut‐off grade. Current reserves are in excess of 20 Mt at similar grade. The ore mineral is bastnasite, and the ore has high light REE/heavy REE (LREE/HREE). The carbonatite is a moderately dipping, tabular 1.4‐Ga intrusive body associated with ultrapotassic alkaline plutons of similar age. The chemistry and ultrapotassic alkaline association of the Mountain Pass deposit suggest a different source than that of most other carbonatites. Elsewhere in the western USA, carbonatites have been proposed as possible REE sources. Large but low‐grade LREE resources are in carbonatite in Colorado and Wyoming. Carbonatite complexes in Canada contain only minor REE resources. Other types of hard‐rock REE deposits in the USA include small iron‐REE deposits in Missouri and New York, and vein deposits in Idaho. Phosphorite and fluorite deposits in the USA also contain minor REE resources. The most recently discovered REE deposit in North America is the Hoidas Lake vein deposit, Saskatchewan, a small but incompletely evaluated resource. Neogene North American placer monazite resources, both marine and continental, are small or in environmentally sensitive areas, and thus unlikely to be mined. Paleoplacer deposits also contain minor resources. Possible future uranium mining of Precambrian conglomerates in the Elliott Lake–Blind River district, Canada, could yield by‐product HREE and Y. REE deposits occur in peralkaline syenitic and granitic rocks in several places in North America. These deposits are typically enriched in HREE, Y, and Zr. Some also have associated Be, Nb, and Ta. The largest such deposits are at Thor Lake and Strange Lake in Canada. A eudialyte syenite deposit at Pajarito Mountain in New Mexico is also probably large, but of lower grade. Similar deposits occur at Kipawa Lake and Lackner Lake in Canada. Future uses of some REE commodities are expected to increase, and growth is likely for REE in new technologies. World reserves, however, are probably sufficient to meet international demand for most REE commodities well into the 21st century. Recent experience shows that Chinese producers are capable of large amounts of REE production, keeping prices low. Most refined REE prices are now at approximately 50% of the 1980s price levels, but there has been recent upward price movement for some REE compounds following Chinese restriction of exports. Because of its grade, size, and relatively simple metallurgy, the Mountain Pass deposit remains North America’s best source of LREE. The future of REE production at Mountain Pass is mostly dependent on REE price levels and on domestic REE marketing potential. The development of new REE deposits in North America is unlikely in the near future. Undeveloped deposits with the most potential are probably large, low‐grade deposits in peralkaline igneous rocks. Competition with established Chinese HREE and Y sources and a developing Australian deposit will be a factor.     

新疆包古图金矿四矿区L7号脉中的特殊矿物组合及其成矿意义

包古图金矿四矿区L7号脉由浅部的自然砷-石英脉型矿石和深部的辉锑矿-石英脉型矿石组成。矿脉中含罕见的As、Sb矿物,如paakkonenite（Sb₂AsS₂）、自然砷、自然锑、方锑金矿、硫锑金银矿（Au₃Ag₄Sb₁₀S₁₂）等。热液过程划分为5个阶段：黄铁矿-毒砂阶段（Ⅰ）,围岩中形成大量的毒砂和黄铁矿并伴随较强硅化;粗粒石英阶段（Ⅱ）,形成沿围岩壁或围岩角砾的梳状石英;Au-As-Sb矿化阶段（Ⅲ）,形成辉锑矿-自然锑-自然砷-paakkonenite-银金矿-自然金-方锑金矿-硫锑金银矿-辉锑银矿-银锌黝铜矿-斜方砷铁矿-硫铜锑矿-石英;晚期Sb矿化阶段（Ⅳ）,形成与粒状方解石共生的辉锑矿、自然锑和paakkonenite;方解石阶段（Ⅴ）,形成穿切矿体和围岩的方解石（-石英）细脉。辉锑矿和斜方砷铁矿交代毒砂,自然金、方锑金矿、paakkonenite和自然砷交代辉锑矿。辉锑矿的结晶主要受温度和还原S含量的控制,自然砷、自然锑的结晶主要受氧逸度和温度控制。As、Sb分别以自然砷、辉锑矿和自然锑形式存在,同时消耗大量H₂S,流体进入张性空间后也释放H₂S,导致硫逸度急剧降低,含Au络合物失稳而成矿。     

Structure and metamorphism of the Calliope Volcanic Assemblage: Implications for middle to Late Devonian orogeny in the northern New England Fold Belt

The Late Silurian to Middle Devonian Calliope Volcanic Assemblage in the Rockhampton region is deformed into a set of northwest‐trending gently plunging folds with steep axial plane cleavage. Folds become tighter and cleavage intensifies towards the bounding Yarrol Fault to the east. These folds and associated cleavage also deformed Carboniferous and Permian rocks, and the age of this deformation is Middle to Late Permian (Hunter‐Bowen Orogeny). In the Stanage Bay area, both the Calliope Volcanic Assemblage and younger strata generally have one cleavage, although here it strikes north to northeast. This cleavage is also considered to be of Hunter‐Bowen age. Metamorphic grade in the Calliope Volcanic Assemblage ranges from prehnite‐pumpellyite to greenschist facies, with higher grades in the more strongly cleaved rocks. In the Rockhampton region the Calliope Volcanic Assemblage is part of a west‐vergent fold and thrust belt, the Yarrol Fault representing a major thrust within this system.

A Late Devonian unconformity followed minor folding of the Calliope Volcanic Assemblage, but no cleavage was formed. The unconformity does not represent a collision between an exotic island arc and continental Australia as previously suggested.     

Rb‐Sr geochronology and Sr isotopic composition of Devonian granitoids,eastern Tasmania

Biotite igneous ages and well‐defined isochron ages of plutons from the composite Blue Tier Batholith and the Coles Bay area in northeastern Tasmania range from 395 to 370 Ma. The older limit of this range, for the George River granodiorite, is considerably older than any age previously recorded for NE Tasmania. The ages of the youngest plutons (Mt Paris and Anchor granites), which host cassiterite ores, record pervasive hydrothermal alteration events. The initial ⁸⁷Sr/⁸⁰Sr ratios of the granitoids range from 0.7061 to 0.7136 and suggest different protolith compositions, consistent with mineralogical and geochemical characteristics of each pluton. The S‐type garnetbiotite granites (Ansons Bay and Booby alia granites) have initial ratios greater than 0.7119, indicative of enriched, high Rb/Sr ratio, crustal source‐rocks of Proterozoic age (1700–800 Ma). The S‐type biotite granites (Poimena and Pearson granites) have relatively high initial ⁸⁷Sr/⁸⁶Sr ratios (0.7070, 0.7105) but overlap with those of the I‐type granodiorites (George River, Scamander Tier, Pyengana and Coles Bay granodiorites) which are in the range of 0.7061 to 0.7073. The initial ratios of the enriched altered plutons are poorly constrained, and on both hand‐specimen and thin‐section scales, reveal open‐system Sr isotopic patterns.

Isochron ages for the arenite‐lutite and lutite sedimentary associations of the Mathinna Beds, which are intruded by the granitoids, reflect an approach to Sr isotopic equilibrium during regional metamorphism. The metamorphic age (401 ± 7 Ma) of the early Pragian arenite‐lutite association indicates a relatively small time interval between deposition, regional metamorphism and granitoid intrusion. The isotopic age for the lutite sedimentary association (423 ± 22 Ma) is tentatively correlated with a Benambran‐age burial metamorphic event that has not previously been recorded in Tasmania.     

Geochemisty and tectonic setting of igneous rocks in the Glenrock Station area,N.S.W.

In the Upper Murray Valley, Victoria, Late Silurian, high‐Si igneous rocks, which are closely associated with alkalic, basaltic dykes, were emplaced at high crustal levels following the peak of the Benambran Orogeny, which deformed and metamorphosed the Wagga Zone in Late Ordovician‐Early Silurian times. These rocks, which are informally termed ‘the Upper Murray high‐Si magmatic suite’, include leucogranites, rhyolite dykes and flows, and ash‐flow tuffs characterised by the following features. They are transitional from mildly peraluminous to mildly metaluminous; they represent relatively anhydrous magmas, in which halides were important volatile constituents; they have high Si, total alkalies, Rb, Th, U, Nb, Sn and heavy rare earth elements; and they are relatively repleted in Mg, Ca, Sr, Eu, V, Cr and Ni. In these respects and in their post‐orogenic setting and close association with alkalic basalts, they resemble many post‐orogenic granitoids from elsewhere. Such granitoids appear to have formed as partial melts during crustal extension following major episodes of deformation and high‐Si magmatism. A residual granulitic crust, from which an earlier generation of granitoid magmas had been extracted, is argued to be the source rock‐type for these post‐orogenic magmas. Tectonic extension, affecting such a crust, was accompanied by deep fracturing and basaltic vol‐canism. Mantle‐derived, CO₂‐ and halide‐rich fluids moved into the residual crust, causing widespread metasomatism, and emplacement of basaltic magma caused temperatures to rise until melting took place and a second group of magmas was produced. This model explains most aspects of the trace and major element chemistry of post‐orogenic, high‐Si igneous rocks and, for the Upper Murray high‐Si suite it also provides an explanation for variations in trace elements and isotopic characteristics. Other processes, such as crystal fractionation, magma mixing, thermogravi‐tational diffusion, and separation and loss of a volatile phase, provide explanations for variations within individual units of the suite, but they do not explain overall variations or the highly fractionated nature of the suite.     

河北省生态环境地球化学

介绍河北省生态环境地球化学特征及其与人体健康、农作物生长等关系。为环境治理、地方病防治、农业生产等需要,提供了区域环境地球化学的基础。     

Soft‐sediment deformation structures in a Pleistocene glaciolacustrine delta and their implications for the recognition of subenvironments in delta deposits

The development of soft‐sediment deformation structures in clastic sediments is now reasonably well‐understood but their development in various deltaic subenvironments is not. A sedimentological analysis of a Pleistocene (ca 13·1 to 15 ¹⁰Be ka) Gilbert‐type glaciolacustine delta with gravity‐induced slides and slumps in the Mosty‐Danowo tunnel valley (north‐western Poland) provides more insight, because the various soft‐sediment deformation structures in these deposits were considered in the context of their specific deltaic subenvironment. The sediments show three main groups of soft‐sediment deformation structures in layers between undeformed sediments. The first group consists of deformed cross‐bedding (inclined, overturned, recumbent, complex and sheath folds), large‐scale folds (recumbent and sheath folds) and pillows forming plastic deformations. The second group comprises pillar structures (isolated and stress), clastic dykes with sand volcanoes and clastic megadykes as examples of water‐escape structures. The third group consists of faults (normal and reverse) and extensional fissures (small fissures and neptunian dykes). Some of the deformations developed shortly after deposition of the deformed sediment, other structures developed later. This development must be ascribed to hydroplastic movement in a quasi‐solid state, and due to fluidization and liquefaction of the rapidly deposited, water‐saturated deltaic sediments. The various types of deformations were triggered by: (i) a high sedimentation rate; (ii) erosion (by wave action or meltwater currents); and (iii) ice‐sheet loading and seasonal changes in the ablation rate. Analysis of these triggers, in combination with the deformational mechanisms, have resulted – on the basis of the spatial distribution of the various types of soft‐sediment deformation structures in the delta under study – in a model for the development of soft‐sediment deformation structures in the topsets, foresets and bottomsets of deltas. This analysis not only increases the understanding of the deformation processes in both modern and ancient deltaic settings but also helps to distinguish between the various subenvironments in ancient deltaic deposits.