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1.
Mineral dust is a major component of the global aerosol, and the importance of dust for regional climate and biogeochemical cycles has become increasingly apparent. By scattering and absorbing radiant energy and through their effects on clouds, dust and other aerosol particles can cause climatic effects that affect ecosystem function and human health. Iron oxide minerals in the atmosphere are especially important in this regard because they absorb solar radiation and are involved in redox reactions. Furthermore, dust particles that settle out of the atmosphere provide nutrients, including iron, to marine ecosystems and other nutrients to terrestrial ecosystems. New technologies have shown that dust reacts in complex ways with other atmospheric constituents; indeed, this is one of the major revelations of recent dust research. Dust and other substances commonly occur in the same air parcels, but bulk chemical methods do not show whether the particles are internally mixed (multiple components mixed in single particles) or externally mixed (admixtures of different particles). Electron beam techniques have shown internal mixtures of dust and black carbon, but the implications of this for climate forcing are still unresolved. Studies conducted with an aerosol time-of-flight mass spectrometer suggest preferential reactions between dust, sulfur and nitrogen oxides, and chlorine. These reactions have important implications for particle formation and solubility, and for the particles' health effects. The activity of radionuclides, including Pu, co-vary with atmospheric dust loads, and while this is not a serious health concern, the emerging view is that pure dust is rarely sampled. While dust can affect ecosystems through climate, the production of dust also is influenced by humans, especially land-use practices that affect vegetative cover. Indeed, the issue of the relative importance of natural vs. anthropogenically-driven changes in dust budgets remains a subject of debate although several recent studies indicate natural variability dominates.  相似文献   

2.
Detailed time-series studies on the major ion geochemistry of tropical peninsular Indian rivers are lacking. In this backdrop, a small stretch of the Godavari River, globally ranking 32nd in terms of total discharge, is chosen for sampling at its mouth. The objectives are: (1) to understand the natural and anthropogenic sources controlling the major ion chemistry of the Godavari River at Rajahmundry, (2) processes controlling the temporal variations in major ions over a period of two years, (3) comparison of total dissolved solid (TDS) fluxes and weathering rates at Godavari River with other major tropical rivers. A total of 47 surface samples were collected, bimonthly, at five stations in the Godavari at Rajahmundry spaced over a distance of 6 km for a period of two years. Water samples were collected in pre-cleaned PP bottles. Parameters like temperature, pH, conductivity, dissolved oxygen, alkalinity were measured on-site. Samples collected for analysis of major ions were processed within a few hours of collection by filtering through 0.45 mm pore size millipore filters. Filtered water samples for major ions were transported to the laboratory in cleaned 250 mL PP bottles. Sodium and K were measured on a Flame Photometer, Ca and Mg on a Flame Atomic Absorption Spectrophotometer, Cl, NO3, SO4 by Ion Chromatography and SiO2 on a spectrophotometer. Chemical weathering of rocks controls the major ion chemistry of the Godavari River at its mouth as indicated by the alkaline nature of the river and dominant presence of Ca, Mg and HCO3 ions. Ca/Mg and Na/Mg ratios point its source to a mixture of lithological assemblages of basalt, granite-granodiorite,  相似文献   

3.
Santiago de Chile is a big city with huge air quality problems, being one of the most polluted cities in the world. This is aggravated during winter by the topography and meteorological conditions of the city. Although public policies have been developed to minimise the atmospheric aerosol pollution, there is a lack of adequate knowledge and poor characterisation of these aerosols (in its PM2.5 and PM10 fractions). In this study we sampled atmospheric particles during winter in two distinct areas of Santiago: downtown (Teatinos Street) and in a more residential area (Macul). Major (Si, Al, Fe, Ca and K) and some trace element (S, Cl, Ti, P, Cr, Cu and Zn) compositions were obtained by proton-induced X-ray emission (PIXE). Morphological, type and chemical characterisation was also performed using scanning electron microscopy (SEM) coupled with an energy dispersive X-ray microanalysis system (SEM–EDX). Besides the carbon particles, the contribution of which can be quite important in the atmospheric aerosol, especially in downtown, unambiguously lithogenic (i.e. of geological origin) particles and elements are the second highest contributors. Enrichment factor calculation, together with particle identification and element correlation allow the origin of some elements and particles to be traced, revealing anthropogenic origins for some of them that are specific to the Santiago area.  相似文献   

4.
《Gondwana Research》2014,25(2):775-796
The Damara Orogeny is a late Neoproterozoic to Cambrian (ca. 570–480 Ma) intracratonic event that affected the Kaoko Belt, the inland branch of the Damara orogen and the Gariep Belt in Namibia and South Africa. This study focuses on the Pan-African evolution of part of the Kaoko Belt between the Puros shear zone and the Village mylonite zone which consists of Mesoproterozoic migmatitic para- and orthogneisses with minor granulite and amphibolite. Pseudosection modeling combined with thermobarometric calculations indicate that the para- and orthogneisses equilibrated at about 670–800 °C and ca. 0.6–0.8 GPa. Some garnets display a pronounced bell-shaped Ca, HREE, Y and Sr zoning, flat zoning profiles of Mn and Fe and concave upward concentration profiles of Sm and Nd. Pressure–temperature estimates obtained on these garnets reveal similar temperatures of 700–750 °C but slightly higher pressures of ca. 0.9 GPa. The preservation of distinct major and trace element zoning in garnet and the existence of broadly similar (near prograde) Sm–Nd and Lu–Hf garnet–whole rock ages of ca. 525 Ma obtained on the same sample indicate an extremely fast cooling path. Retrograde conditions persisted until ca. 490 Ma indicating a slow, late stage near isobaric cooling path. The resulting clockwise P–T–t path is consistent with crustal thickening through continent–continent collision followed by post-collisional extension and suggests that the upper amphibolite to granulite facies terrain of the central Kaoko Belt formed initially in a metamorphic field gradient of ca. 25–35 °C km 1 at moderately high pressures.  相似文献   

5.
6.
The front of the Zoulang Nanshan Caledonian volcanic island arc zone in the northern Qilian Mountains is a forearc accretionary terrane, composed of multiple accretionary volcanic island arcs, flysch accretionary wedges,high-pressure metamorphosed detachment zones and remnants of ophiolites. It resulted from the northeastward subduction of the Early Palaeozoic Qilan oceanic crust beneath the Alxa block. High-pressure metamorphism, which occurred during the subduction, progressed through three stages: the initial stage of medium T-high P,the main stage of temperature decrease and pressure increase, and the lag stage of pressure decrease and temperature increase. Finally the paper presents a retrotrench subduction dynamic model indicative of northward subduction of the central Qilian block and southward accretion of the Alxa block during the period of 450-500 Ma.  相似文献   

7.
8.
Zircon, monazite, and xenotime have proven to be valuable chronometers for various geological processes due to their commonly high-U–Th and low common Pb contents. However, zircons that have crystallized in highly fractionated granites often have such high-U contents that radiation damage can lead to scattered U–Pb ages when measured with secondary ion mass spectrometry (SIMS). In this study, monazite and xenotime were separated from a number of highly fractionated granites at the Xihuashan tungsten mine, Southeast China, for alternative dating methods by SIMS. For monazite analysis, obvious excess 204Pb signal (mainly from interference of 232Th144Nd16O2 ++) was observed in high-Th (>2 wt%) monazite, which hinders 204Pb-based common Pb corrections. A 207Pb-based common Pb correction method was used instead. By employing power law relationships between Pb+/U+ versus UO2 +/U+, Pb+/Th+ versus ThO2 +/Th+ and suitable exponentials, monazites with ThO2 contents in the range of ~3–19 % do not exhibit this matrix effect. Independent SIMS U–Pb ages and Th–Pb ages of three phases of Xihuashan granite samples were consistent with each other and yielded dates of 158.7 ± 0.7, 158.0 ± 0.7, and 156.9 ± 0.7 Ma, respectively. Xenotime does show marked matrix effects due to variations of U, Th, and Y [or total rare earth element (REE), referred as ΣREE hereafter] contents. Suitable correction factors require end-member standards with extremely high or low U, Th, and Y (or ΣREE) contents. No excess 204Pb was observed, indicating that the 204Pb-based common Pb correction method is feasible. Independent 207Pb/206Pb ages can be obtained, although multi-collector mode is necessary to improve precision. The main difficulties with dating xenotime are when high-Th (U) mineral inclusions are ablated. We can identify when this occurs, however, by comparing the measured UO2 +/U+ and ThO2 +/Th+ with those in xenotime standards. Three xenotime samples from the first phase of Xihuashan granite yielded a weighted mean 207Pb/206Pb date of 159.5 ± 4.4 Ma (MSWD = 1.0) and a 206Pb/238U date of 159.4 ± 0.9 Ma (MSWD = 1.6), which are consistent with monazite U–Pb and Th–Pb ages from the same granites. This study demonstrates that monazite and xenotime are better SIMS chronometers for highly fractionated granites than zircon, which can yield doubtful ages due to high-U contents.  相似文献   

9.
Variations in the abundances of Zn, Cu, and Pb are found to be useful in identifying tectonic regimes and separating oceanisland basalts into enriched- and depleted-source categories. The average Zn, Cu, and Pb contents of normal mid-ocean ridge basalts (N-MORB) are 84, 70, and 0.35 ppm, respectively. Differences in average Zn contents for various ridges reflect more the varying degrees of differentiation than variations of Zn content in the source rocks. At a Mg# of 70, or Mg#70, which is taken to represent primitive MORB, many MORB sequences converge at a Zn content of 58 ± 6 ppm, which is close to the value for primitive mantle (50 ppm) and ordinary chondrites (~55 ppm). Values of 0.1 to 0.15 ppm Pb in MORB at Mg#70, best defined at the superfast-spreading Southern East Pacific Rise, are similar to estimates of Pb in the primitive mantle (0.12 to 0.18 ppm). They also are near the lower end of the range for ordinary chondrites. The very slow spreading Southwest Indian Ocean Ridge has a sequence with higher Pb contents, in addition to a more normal sequence, which has a visual best value of 0.4 ppm Pb at Mg#70. With the exception of the Walvis Ridge, Zn and Cu appear to be little affected by proximity to hotspots (i.e., E-MORB); however, Pb contents are higher and average about 0.6 ppm.

Both Zn and Pb in MORB are incompatible elements (i.e., favor the melt), but Cu is a compatible element. At Mg#70, there is the suggestion of a value of 100 ppm for Cu, with lower values possibly representing partial removal of sulfides and their associated Cu from the source. Nonetheless, Cu contents of primitive MORB tend to be much higher than even high estimates for the primitive mantle (28 ppm), and are closer to ordinary chondrites (~90 ppm). Therefore, Zn, Cu, and Pb all approximate chondritic values in the primitive MORB melt.

Average contents of Zn, Cu, and Pb in oceanic island basalts (OIB) are 115, 62, and 3.2 ppm, respectively. At Mg#70, values of Zn and Cu are similar to the respective averages for OIB, with Zn higher and Cu lower than MORB. At a Mg# of ~40, however, OIB and MORB tend to have similar Zn contents. With further differentiation, OIB trachytes can contain >200 ppm Zn. Unlike MORB, OIB can differentiate to high Cu contents of 200 ppm at Mg#s of 40 to 60. In contrast to Zn and Cu, Pb regresses to a value of 0.83 ppm at Mg#70 for Hawaiian and Reunion volcanics, which is much less than the average value for Pb in OIB volcanics, but higher than for MORB.

Average Zn, Cu, and Pb contents of magmatic-arc basalts are 77, 108, and 1.9 ppm, respectively. In basalts, Zn tends to be incompatible, but a dual incompatible and compatible behavior can occur at high SiO2 contents. Dacites may average near 55 ppm Zn, but peralkalic rhyolite can contain >300 ppm Zn. A dual compatible and incompatible nature occurs for Cu. Most common, particularly in submarine volcanics, is a compatible trend, with a Cu content of around 80 ppm at a Mg# of 60, which decreases to less than 40 ppm at a Mg# of 30. The incompatible trend of increasing Cu can achieve >200 ppm at a Mg# of 30, leaving a gap approaching 100 ppm at that Mg#. The gap is less obvious on a plot of Cu vs. SiO2, but is still there. The compatible trend is proposed to result from sulfur-saturated magmas, whereas the incompatible trend is believed to result from sulfur-deficient magmas. Support for this hypothesis is found in sparse sulfur-isotope data. Zn and Cu both can be incompatible over an extended range of Mg#s or silica content. When Zn and Cu are both compatible, Cu decreases more than twice as rapidly as Zn.

Primitive magmas at Mg#70 average about 50 ppm Zn for submarine Mariana arc basalts and 58 ppm for forearc boninites, contents close to MORB values. Mariana arc basalts have a Zn content of ~45 ppm estimated at Mg#70. Cu varies more widely than Zn in primitive magmas, being about 50 ppm Cu for Mariana Islands volcanics and 120 ppm for Kermadec Islands volcanics, a range broadly around MORB values. Average Pb contents are 1.9 ppm for island-arc tholeiites, 5.6 ppm for high-Al basalt, and 3.2 ppm for alkali basalt with average boninite of approximately 1.8 ppm. Back-arc-basin basalts in the deepest parts of the Mariana trough have Pb contents of 0.45 ppm, but more shallow parts may exceed 1.0 ppm Pb. Although the lower contents are similar to MORB values, the 208Pb/204Pb values are greater than Pacific Ocean MORB. At Mg#70 for rocks from the Tonga and Kermadec island arcs, the Pb content is about 0.1 ppm, similar to MORB.  相似文献   

10.
True graphic quartz structures in pegmatites from Carrara/Giggiga and Harrar (town) districts of Ethiopia, are compared with the micrographic quartz textures in the Rapakiwi granite of Finland. Graphic-like textures of uraninite in microcline are also discussed and compared with these graphic structures.A quartz vein, about 1–2 meters in thickness, intersects a pegmatite in the Carrara/Giggiga district. This quartz vein extends into the microcline of the pegmatite as fine quartz veins which attain the form and character of graphic quartz. Also the graphic quartz of the Harrar pegmatites is observed to extend into and occupy cracks in the microcline.Comparable in origin to these graphic textures is the micrographic quartz in the Rapakiwi granite. Observations show micrographic quartz following the cleavage directions in the orthoclase as well as the interzonal spaces and the boundaries of inclusions in the K-feldspar.On the basis of the observed structures and textures these graphic and micrographic intergrowths are considered to be due to solutions penetrating or infiltrating into existing structures and not due to simultaneous crystallisation as conditions of eutectic crystallisation would require.In addition to the well known graphic structures there occur graphic or myrmekitic-like intergrowths of uraninite in microcline which, from a structural and physico-chemical point of view, cannot be considered to be due to eutectic crystallisation.  相似文献   

11.
Fine atmospheric dust includes mineral particles and aggregates, fibrous minerals and fibrous organic material. Generation, dislodgement and transport (deflation) of natural dust with the finer (〈4 microns) components suspended as silt-size aggregates, is widespread in and adjacent to the world's drylands, as well as deriving from volcanic vents. Silica is a highly fibrogenic agent in lung tissue. Long-term inhaling of siliceous dusts can lead to a number of fibrotic lung diseases, including natural (non-occupational) pneumoconioses (notably silicosis, but including asbestosis and others). Different polymorphs of silica show different levels of toxicity in interaction with lung tissue. Particles with highly active surfaces may release radicals, causing cell damage. Some types of inhaled particulates are degraded by macrophages, but many are highly resistant and persist in the lungs, some stimulating fibroblastic cells to deposit collagen. Silicosis is an inflammation of the lung commonly caused by silicate mineral particles, leading to fibrosis. Three types are recognized: nodular pulmonary fibrosis (simple or chronic silicosis), acute silicosis, and accelerated silicosis. Generally, finer particulates have greater oxidative capacity than the coarser fractions. They contain more reactive oxygen species, their greater bioreactivity making them more toxic to pulmonary tissue. Nevertheless, inhalation of large dust particles (〉 10μm) may constitute a health risk if the mineralogy is toxic, regardless of where the grains lodge in the respiratory system. Dust may absorb harmful gases, disease-generating bacteria and carcinogenic hydrocarbon compounds. Silica-related respiratory disease may also an exacerbate cardiac problem, and epidemiology suggests a link with tuberculosis. Quantification of dust loading and exposure requires study of spatial and temporal patterns, supported by meteorological analysis, airflow modeling and satellite-borne imagery. Some acute, short-term health impacts have been assessed using atmospheric and health records both before and after a dust storm or by comparison of populations within and outside such events. Analysis of the size, shape, mineralogy and geochemistry of ambient dust particulates provides information on natural dust sources, dust concentrations, and potential particulate toxicity, as well as providing a datum for assessment of human exposure levels.  相似文献   

12.
The complex study of the river water and pore solutions from the bottom sediments in the lower reaches of the Razdol’naya River was conducted in February 2010. The major ion composition of the waters indicates the submarine origin of the near-bottom and pore waters in the lower reaches of the Razdol’naya River in the winter. The river estuary extends upstream for more than 20 km. It was established that the studied sediments are reduced oozes containing pyrite, hydrotroilite, and iron monosulfide, which is direct evidence for sulfate-reduction in the sediments. The diagenesis of organic matter is the main reason for the considerable decrease in the amount of sulfates and the increase in the alkalinity of the sediment pore water. The sedimentary pore water sampled from the deep river pits is characterized by excess alkalinity that cannot be explained by sulfate-reduction and methane genesis. It was suggested that the chemical weathering of silicate minerals and the bacterial mineralization of salts of organic acids could result in the excess alkalinity of the sediment pore water.  相似文献   

13.
Asteroid impact spherule layers and tsunami deposits underlying banded iron-formations in the Fortescue and Hamersley Groups have been further investigated to test their potential stratigraphic relationships. This work has included new observations related to the ca 2.63 Ga Jeerinah Impact Layer (JIL) and impact spherules associated with the 4th Shale-Macroband of the Dales Gorge Iron Member (DGS4) of the Brockman Iron Formation. A unit of impact spherules (microkrystite) correlated with the ca 2.63 Ga JIL is observed within a >100 m-thick fragmental-intraclast breccia pile in drill cores near Roy Hill. The sequence represents significant thickening of the impact/tsunami unit relative to the JIL type section at Hesta, as well as relative to the 20–30 m-thick ca 2.63 Ga Carawine Dolomite spherule-bearing mega-breccia. The ca 2.48 Ga-old Dales Gorge Member of the Brockman Iron Formation is underlain by an ?0.5 m-thick rip-up clast breccia located at the top of the ca 2.50 Ga Mt McRae Shale, and is interpreted as a tsunami deposit. We suggest that the presence of impact ejecta and tsunami units stratigraphically beneath a number of banded iron-formations, and units of ferruginous shale in the Pilbara and South Africa may result from a genetic relationship. For example, it could be that under Archean atmospheric conditions, mafic volcanism triggered by large asteroid impacts enriched the oceans in soluble FeO. If so, seasonal microbial and/or photolytic oxidation to ferric oxide could have caused precipitation of Fe2O3 and silica. In view of the possible occurrence of depositional gaps and paraconformities between impact ejecta units and overlying ferruginous sediments, these relationships require further testing by isotopic age studies.  相似文献   

14.
This study is aimed at determining the diffusion coefficient of net-work modifiers (mainly Na, K, and Ca) in a two-phase melt-NaCl system, in which the melts are granitic and the system is NaCl-rich in composition. The diffusion coefficients of Na, K, and Ca were measured at the temperatures of 750 – 1400°C, pressures of 0.001 × 108 – 2 × 108 Pa, and initial H2O contents of 0 wt% –6.9 wt% in the granitic melts. The diffusion coefficients of Fe and Mg were difficult to resolve. In all experiments a NaCl melt was present as well. In the absence of H2O, the diffusion of net-work modifiers follows an Arrhanious equation at 1 × 105 Pa: lgDca=−3. 88−5140/T, lgDk =−3. 79−4040/T, and lgDNa, =−4.99−3350/T, where D is in cm2 /s andT is in K. The diffusion coefficients of Ca, Na, K, and Fe increase non-linearly with increasing H2O content in the melt. The presence of about 2 wt% H2O m the melt will lead to a dramatical increase in diffusivity, but higher H2O content has only a minor effect. This change is probably the result of a change in the melt structure when H2O is present. The diffusion coefficients measured in this study are significantly different from those in previous works. This may be understood in terms of the “transient two-liquid equilibrium” theory. Element interdiffusion depends not only on its concentration, but also on its activity co-efficient gradient, which is reflected by the distribution coefficient, of the two contacting melts.  相似文献   

15.
The characteristic structures of the Precambrian cherts from the Gusui section, Guangdong ,Chi-na, include bedded structure ,laminated structure ,massive structure and pseudobrecciated structure.The chert is characterized by consistently low abundance of TiO2,Al2O3 and most trace elements.Howevver ,it is enriched in Ba,As,Sb,Hg and Se.In Al-Fe-Mn ternary diagrams,it falls into the “hydrothermal field“ .Correspondence analysis and factor analysis show that many elements show up in the factor that represents the leaching of country rocks by hydrothermal solutions,and are the very characteristic element association fo the geochemically anomalous South China basement.Petrologic and geochemical evidence suggests a hydrothermal origin for the chert.The chert may have been formed in a Precambrian fift or an extension zone developed within the Yunkai marginal geosyncline, with a fault system linking it to an unknown heat source at depth.  相似文献   

16.
We dissolved Boulder Creek Granodiorite in a plug flow reactor for 5794 h at pH = 1 and T = 25 °C. The primary purpose of the experiment was to identify controls on dissolved δ44/40Ca, δ44/42Ca, and δ26/24Mg values during granite weathering. Herein, we also examine the origin of Ca and Mg isotopic variability among minerals composing the Boulder Creek Granodiorite, and we constrain fundamental characteristics of granite weathering important for quantifying the elemental and isotopic geochemistry of the reactor output. Nine Ca-bearing minerals display an 8.80‰ range of δ44/40Ca values and a 0.51‰ range of δ44/42Ca values. Three Mg-bearing minerals display a 1.53‰ range of δ26/24Mg values. These ranges expressed at the mineralogical scale are higher than the ranges thus far reported for bulk igneous rocks. Most of the δ44/40Ca variability reflects 40Ca enrichment in K-feldspar, and to a lesser extent, biotite, due to the radioactive decay of 40K over the 1.7 Ga age of the rock, whereas the entire range of δ44/42Ca values reflects mass-dependent isotope fractionation during igneous differentiation and crystallization. The range of δ26/24Mg values may represent either fractionation during the chloritization of biotite or interaction of the Boulder Creek Granodiorite with Mg-rich metamorphic fluids having low δ26/24Mg values.The elemental and isotopic composition of the reactor output varied substantially during the experiment. We synthesize the mineralogical and fluid data using coupled mass-conservation equations solved at non-steady-state. Model calculations reveal an intricate balance between increasing specific surface area and decreasing mineral concentrations. While surface area normalized dissolution rate constants were time-invariant, specific surface area increased as a power-law function of time through positive feedbacks between mechanical disaggregation, chemical dissolution, and mineral depletion. Variations in dissolved δ44/40Ca, δ44/42Ca, and δ26/24Mg values reflect conservative mixing rather than fractionation. Apatite and calcite initially control δ44/40Ca and δ44/42Ca values, followed by biotite, titanite, epidote, hornblende, and plagioclase. The release of radiogenic 40Ca clearly defines the period where biotite dissolution dominates. The brucite layer of chlorite initially controls δ26/24Mg values, followed by biotite, the TOT layer of chlorite, and hornblende. Through direct isotopic tracking, these results demonstrate that trace minerals, such as apatite and calcite in the case of Ca and brucite in the case of Mg, dominate elemental release during the incipient stages of granite weathering. The results further show that biotite dissolution dominates the middle stages of granite weathering and that plagioclase dissolution only becomes important during relatively late stages. The Ca and Mg isotope variations associated with these stages are distinct and potentially resolvable in soil mineral weathering studies.  相似文献   

17.
Epochs of changing atmospheric CO2 and seawater CO2–carbonic acid system chemistry and acidification have occurred during the Phanerozoic at various time scales. On the longer geologic time scale, as sea level rose and fell and continental free board decreased and increased, respectively, the riverine fluxes of Ca, Mg, DIC, and total alkalinity to the coastal ocean varied and helped regulate the C chemistry of seawater, but nevertheless there were major epochs of ocean acidification (OA). On the shorter glacial–interglacial time scale from the Last Glacial Maximum (LGM) to late preindustrial time, riverine fluxes of DIC, total alkalinity, and N and P nutrients increased and along with rising sea level, atmospheric PCO2 and temperature led, among other changes, to a slightly deceasing pH of coastal and open ocean waters, and to increasing net ecosystem calcification and decreasing net heterotrophy in coastal ocean waters. From late preindustrial time to the present and projected into the 21st century, human activities, such as fossil fuel and land-use emissions of CO2 to the atmosphere, increasing application of N and P nutrient subsidies and combustion N to the landscape, and sewage discharges of C, N, P have led, and will continue to lead, to significant modifications of coastal ocean waters. The changes include a rapid decline in pH and carbonate saturation state (modern problem of ocean acidification), a shift toward dissolution of carbonate substrates exceeding production, potentially leading to the “demise” of the coral reefs, reversal of the direction of the sea-to-air flux of CO2 and enhanced biological production and burial of organic C, a small sink of anthropogenic CO2, accompanied by a continuous trend toward increasing autotrophy in coastal waters.  相似文献   

18.
Perovskite, a common Th- and U-enriched accessory mineral crystallised from kimberlitic magmas, has long been thought to be an important geochronometer for dating the emplacement of kimberlite. However, it also contains variably high levels of common Pb, which makes it difficult to obtain a precise measurement of radiogenic Pb/U and Pb/Th isotopic compositions using microbeam techniques such as SIMS and LA-ICP-MS. We present calibration protocols for in situ U–Pb and Th–Pb age determination of kimberlitic perovskite using the large double-focusing Cameca IMS 1280. Linear relationships are found between ln(206Pb?+/U+) and ln(UO2+/U+), and between ln(208Pb?+/Th+) and ln(ThO+/Th+), based on which the inter-element fractionation in unknown samples during SIMS analyses can be precisely calibrated against a perovskite standard. The well-characterized Ice River perovskite is chosen as the U–Pb and Th–Pb age standard in this study. The 204Pb-correction method was used to estimate the fraction of common Pb, which is consistent with the results obtained using the 207Pb-based correction method for the dated perovskites of Phanerozoic age.A Tazheran perovskite with unusually high U but rather low Th yielded a Concordia U–Pb age of 462.8 ± 2.5 Ma and a Th–Pb age of 462 ± 4 Ma. Two perovskite samples from the Iron Mountain kimberlite have identical Concordia U–Pb ages of 410.8 ± 3.4 Ma and 411.0 ± 2.6 Ma, which are consistent within errors with their corresponding Th–Pb ages of 409.2 ± 7.2 Ma and 412.3 ± 3.3 Ma, respectively. Two perovskite samples from the Wesselton Mine of South Africa yielded indistinguishable 206Pb/238U ages of 91.5 ± 2.2 Ma and 90.3 ± 2.9 Ma, and Th–Pb ages of 90.5 ± 0.8 Ma and 88.4 ± 1.6 Ma, respectively. Accuracy and precision of 1–2% (95% confidence level) for these measurements have been demonstrated by the consistency of their U–Pb and Th–Pb ages with the recommended U–Pb ages of previous works.  相似文献   

19.
A May 2007 tornado destroyed 95% of aging, declining Greensburg, Kansas. The city took the opportunity to build back “stronger, better, and greener,” enforcing upgraded codes, requiring city-owned buildings to meet LEED Platinum level standards, and recommending energy-efficiency housing in a new Sustainable Comprehensive Plan. Using information collected from surveys of Greensburg tornado survivors, interviews, and publications, we examined the housing-related recovery, including the emergency provision of temporary shelter and rebuilding permanently. Although temporary shelter kept residents nearby for rebuilding, given the gap between insurance policy limits on the aging housing stock and rebuilding costs, housing affordability is a critical issue in Greensburg’s recovery. Local, state, and federal support have made construction of municipal buildings at LEED Platinum level and some affordable and green housing projects possible. However, far greater public and private sector funding for affordable workforce housing, in conjunction with broader economic and job development, is needed.  相似文献   

20.
This article explores the role of geographical context in generating a stigmatised identity among residents of Tara rural subdivisions in the coal seam gas fields in Queensland’s Western Downs. The research was based on qualitative interviews with Tara ‘Blockies’, as these residents are commonly referred to, that revealed how their existence in the middle of an agrarian region resulted in the assignation of a stigma that has marked them as different, and subsequently devalued their status. We explain that this distinction and category division of the normals, referring to Tara’s Agrarian residents, from the ‘stigmatised’ led to an antagonistic relationship that prevented successful socio-cultural assimilation. We demonstrate how an immoral place becomes disadvantaged, resulting in poor well-being, and how imposed labels threaten the self-esteem of its occupants.  相似文献   

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