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1.
In the present study, we explored the use of various optical parameters to detect differences in the composition of the dissolved organic matter (DOM) in a set of lakes that are all located on the Canadian Precambrian Shield, but within which Cu and Ni speciation predictions were previously shown to diverge from measured values in some lakes but not in others. Water samples were collected with in situ diffusion samplers in 2007 (N = 18 lakes) and 2008 (N = 8 lakes). Significant differences in DOM quality were identified between the sampling regions (Rouyn-Noranda, Québec and Sudbury, Ontario) and among lakes, based on dissolved organic carbon concentrations ([DOC]), specific UV absorbance (SUVA254), fluorescence indices (FI), and excitation–emission matrix (EEM) fluorescence measurements. Parallel factor analysis (PARAFAC) of the EEM spectra revealed four components, two of which (C3, oxidized quinone fluorophore of allochthonous origin, and C4, tryptophan-like protein fluorescence of autochthonous origin) showed the greatest inter-regional variation. The inter-lake differences in DOM quality were consistent with the regional watershed characteristics as determined from satellite imagery (e.g., watershed-to-lake surface area ratios and relative percentages of surface water, rock outcrops vegetative cover and urban development). Source apportionment plots, built upon PARAFAC components ratios calculated for our lakes, were used to discriminate among DOM sources and to compare them to sources identified in the literature. These results have implications for other areas of research, such as quantifying lake-to-lake variations in the influence of organic matter on the speciation of trace elements in natural aquatic environments.  相似文献   

2.
Conventional fluorescence microscopy and visible light region fluorescence microspectrometry have been combined with laser scanning fluorescence microscopy (LSFM) to examine and characterize soluble sedimentary organic matter (SOM) in Holocene diatomaceous laminites from ODP core 1034, Saanich Inlet, British Columbia, Canada. Microscopic SOM in the laminites is dominated by two components: red-fluorescing chlorophyllinite, and yellow-fluorescing, diatom-derived oils. Both are commonly preserved within the interior of siliceous diatom auxospores and appear as an abundant and intense stain on mineral matter throughout the laminites. The mineral stain is classified as matrix chlorophyllinite and matrix oil, respectively. Accessory insoluble SOM consists of dinoflagellate, prasinophyte and coccoidal alginites, and rare woody huminite, funginite, and sporinite. Visible light region fluorescence microspectrometry of chlorophyllinite reveals a predominance at λ max 670–675 nm, which is consistent with a chlorophyll a source based on comparison with reference samples of chlorophyll a and b. The consistency in λmax and spectral character of chlorophyllinite with increasing depth in Saanich Inlet correlates with a high degree of chlorophyll preservation. Its distribution in the laminites is readily imaged by LSFM using either UV (363 nm) or blue (488 nm) laser excitation and >665 nm emission. Yellow-fluorescing diatom oils have λmax ranging from 485 to 520 nm, suggesting that they may comprise up to 70% saturates. The distribution of entrapped yellow-fluorescing diatom oils as well as matrix oils is also readily imaged with LSFM using a combination of UV laser excitation (363 nm) and 510 ±40 nm emission. Laminae in the Saanich Inlet samples which are highly enriched in both diatom oils and ‘reproductive’ auxospore cells are interpreted as recording intense episodic spring diatom blooms. The observations reported here document microscopically, in situ, possibly pristine preservation of diatom oils (including possible fatty acids) at appreciable depths within Holocene organic-rich laminites. Their recognition in recent and older strata is important, for they serve as potential biomarkers for assessing long term geo-environmental changes such as water temperature. The periodic presence of anomalously high amounts of diatom-derived biological oils in laminae within the recent sediments may mark times of unusually high nutrient levels and paleoproductivity.  相似文献   

3.
The concentrations of atmospheric and dissolved carbonyl sulfide (COS) were measured during a Lagrangian study aboard the R/V Meteor in the northeast Atlantic Ocean, April/May 1992, and during a campaign on the research platform Nordsee in the German Bight (southeastern North Sea), September 1992. The arithmetic means and standard deviations of the COS saturation ratios were 1.27 ± 0.58 (northeast Atlantic) and 3.23 ± 0.73 (German Bight). Sea surface COS showed a pronounced diel cycle with highest concentrations in the late afternoon and a mean concentration amplitude of about 2. To account for this diel cycle, we analyze our results using a simple empirical model, which includes a zeroth order photoproduction constant, sea surface UV light intensity, and terms for hydrolysis removal and air-sea exchange. Fitted and observed COS concentrations agreed to within11 % (northeast Atlantic) and 14% (German Bight). The in situ COS photoproduction constants were (0.030 ± 0.008) fmol L–1 s–1 W–1 m2 in the northeast Atlantic (n = 8) and (0.17 ± 0.07) fmol L–1 s–1 W–1 m2 in the German Bight (n = 10). After normalization to the cloud cover corrected UV irradiance at 40 latitude, we obtained sea surface COS production rates of (0.034 ± 0.017) nmol L–1 d–1 in the northeast Atlantic and (1.62 ± 0.62) nmol L–1 d–1 in the German Bight. Currently available in situ photoproduction rates show a high degree of correlation with the UV absorbance (r 2 = 0.98, n = 4) and fluorescence (r 2 = 0.85, n = 4) of chromophoric dissolved organic matter (CDOM). The regional differences between the COS productivity in the northeast Atlantic Ocean and the German Bight is attributed to the distribution pattern of CDOM optical properties.  相似文献   

4.
Carbonaceous matter (CM) from ca. 3.5 Ga hydrothermal black cherts of the Pilbara Craton of Western Australia and the Barberton Greenstone Belt of South Africa yielded transmission electron microscopy (TEM) images that are suggestive of microbial remains and possible remnants of microbial cell walls. These are compared to a potential modern analogue, the hyperthermophilic Methanocaldococcus jannaschii, derived from an active seafloor hydrothermal environment and cultured under similar conditions. A striking resemblance to the early Archaean forms was evident in wall structure and thermal degradation mode. Cell disintegration of the cultures occurred at 100 °C marking the limits of life. Complete disintegration, deformation and shrinkage occurred at 132 °C. A multidisciplinary approach to the characterisation of the CM was undertaken using organic petrology, TEM coupled with electron dispersive spectral analysis (EDS), high resolution TEM (HRTEM) to determine molecular ordering, and elemental and carbon isotope geochemistry. Reflectance measurements of the CM to determine thermal stress yielded a range of values corresponding to several populations, and pointing to different sources and processes. The δ13C values of Dresser Formation CM (−36.5 to −32.1‰) are negatively correlated with TOC (0.13–0.75%) and positively correlated with C/N ratio (134–569), which is interpreted to reflect the relative abundance of high Ro/oxidised/recycled CM and preferential loss of 12C and N during thermal maturation. TEM observations, inferred carbon isotopic heterogeneity and isotope fractionations of −27 to −32‰ are consistent with the activity of chemosynthetic microbes in a seafloor hydrothermal system where rapid silicification at relatively low temperature preserved the CM.  相似文献   

5.
The dehydration rate of hydrous rhyolitic glasses at 475–875 °C was measured by in situ infrared (IR) spectroscopy in order to determine the diffusion coefficient of water in rhyolitic glasses. The IR spectra of glass thin sections were obtained at 90-s intervals during 90 min at high temperatures, and the change in absorbance at 3550 cm–1 corresponding to total water was monitored. The diffusion coefficients obtained from dehydration rates of the rhyolitic glasses are considered to be averaged value over the water-concentration profile in the sample. The averaged apparent diffusion coefficients increase with the initial total water content from 0.20 m2 s–1 for 0.7 wt% to 0.37 m2 s–1 for 2.8 wt% at 700 °C. The apparent activation energy for the diffusion of total water decreases with increasing initial water content from 112 ± 6 kJ mol–1 for 0.7 wt% to 60 ± 17 kJ mol–1 for 4.1 wt%. Assuming a linear relation between the diffusion coefficient of total water and the total water content, the diffusion coefficients at each initial total water content were also determined. The diffusion coefficients of total water at the water contents of 0.7 and 1.9 wt% and at 0.1 MPa were best fitted by ln D=[(12.9 ± 0.8) – (111 500 ± 6400)/RT] and ln D=[(10.6 ± 0.4) – (86 800 ± 2800)/RT], respectively, and are in agreement with previous data (D in m2 s–1, T in K). The present in situ IR dehydration experiment is a rapid and effective method for the determination of water diffusivity at high temperatures.  相似文献   

6.
The local and geometrical structure around gold (III) e.g., Au3+ ions in aqueous solution with different OH−/Cl− molar ratios, has been investigated by X-ray absorption spectroscopy (XAS). X-ray absorption near-edge structure (XANES) spectra of [AuCln(OH)4−n]− solutions have been calculated and the multiple-scattering spectral features have been attributed to Cl d-states, axial water molecules and the replacement of Cl− ligands by OH− ligands. A square–planar geometry for [AuCln(OH)4−n]− with two axial water molecules has been identified. Moreover, a spectral correlation between XANES features and the type of planar atoms has been identified. By extended X-ray absorption fine structure spectra (EXAFS), the planar Au bond distances in the solutions have also been determined, e.g., 2.28 Å for Au–Cl and 1.98 Å for Au–O, respectively. The same EXAFS analysis provides evidence that the peak at about 4.0 Å in solutions with the lowest OH−/Cl− molar ratio arises from collinear Cl–Au–Cl multiple-scattering contributions. For the first time, a complete detailed reconstruction of the hydration structure of an Au ion at different pH values has been achieved.  相似文献   

7.
The concentration and biomarker compositions of sedimentary organic matter (OM) as well as fine and coarse suspended particles were analysed to identify the impact of deforestation on the transport of terrigenous organic matter (OM) in the Rio Tapajós, a major tributary to the Amazon. Substantial shifts in the concentration and composition of recently deposited sedimentary OM suggest that intensive deforestation over the last few decades has considerably modified the natural inputs of sedimentary materials to the aquatic ecosystems by disrupting the terrigenous fluxes of humus and soil materials from the drainage basin. The observed compositional changes of bulk OM and land derived biomarkers (e.g. lignin) in recent sediments illustrate a sedimentary enrichment in OM from soil horizons that, under normal forest cover, tend to be retained in the drainage basin. On average, the recently accumulated OM is nitrogen-rich ((C/N)a=12–15) and more highly degraded ((Ac/Al)v=0.4–0.6 and DHBA/V=0.15–0.20) than deep materials ((C/N)a=20–30, (Ac/Al)v=0.25–0.4, and DHBA/V=0.05–0.10), showing that this recently accumulated material is more humified than original inputs to the aquatic system, and consistent with increased exportation of fine eroded mineral and organic particles from surface soils along river banks. The present study illustrates the relevance of using OM oxidation products in sediment profiles to evaluate deforestation impacts on aquatic ecosystems and to characterize the nature of eroded soil materials, complementing studies on mineral/metal cycling.  相似文献   

8.
Pure forsterite crystals were grown from hydrous melts using controlled cooling experiments at 2.0 GPa and varying the bulk Mg/Si ratio from 2.0 to 1.5. Oriented single crystals were then studied by polarised infrared spectroscopy. The spectra of the samples with the lowest silica activity (aSiO2) contain the main OH bands in the range 3,620–3,450 cm–1 only. In contrast, the spectra of the samples synthesised with the highest aSiO2 contain additional pleochroic bands at 3,160, 3,220 and 3,600 cm–1. The variations are interpreted in terms of protonated silicon vacancies being dominant at low aSiO2 and Mg vacancies dominant at high aSiO2. Xenolithic mantle olivines generally do not have the spectrum expected for orthopyroxene buffered conditions, suggesting that they re-equilibrated with their host melts during ascent, but mantle olivine from the Zabargad peridotite massif probably is in equilibrium with the coexisting orthopyroxene.Editorial responsibility: T.L. Grove  相似文献   

9.
D.R. Gray  D.A. Foster   《Tectonophysics》2004,385(1-4):181-210
Structural thickening of the Torlesse accretionary wedge via juxtaposition of arc-derived greywackes (Caples Terrane) and quartzo-feldspathic greywackes (Torlesse Terrane) at 120 Ma formed a belt of schist (Otago Schist) with distinct mica fabrics defining (i) schistosity, (ii) transposition layering and (iii) crenulation cleavage. Thirty-five 40Ar/39Ar step-heating experiments on these micas and whole rock micaceous fabrics from the Otago Schist have shown that the main metamorphism and deformation occurred between 160 and 140 Ma (recorded in the low grade flanks) through 120 Ma (shear zone deformation). This was followed either by very gradual cooling or no cooling until about 110 Ma, with some form of extensional (tectonic) exhumation and cooling of the high-grade metamorphic core between 109 and 100 Ma. Major shear zones separating the low-grade and high-grade parts of the schist define regions of separate and distinct apparent age groupings that underwent different thermo-tectonic histories. Apparent ages on the low-grade north flank (hanging wall to the Hyde-Macraes and Rise and Shine Shear Zones) range from 145 to 159 Ma (n=8), whereas on the low-grade south flank (hanging wall to the Remarkables Shear Zone or Caples Terrane) range from 144 to 156 Ma (n=5). Most of these samples show complex age spectra caused by mixing between radiogenic argon released from neocrystalline metamorphic mica and lesser detrital mica. Several of the hanging wall samples with ages of 144–147 Ma show no evidence for detrital contamination in thin section or in the form of the age spectra. Apparent ages from the high-grade metamorphic core (garnet–biotite–albite zone) range from 131 to 106 Ma (n=13) with a strong grouping 113–109 Ma (n=7) in the immediate footwall to the major Remarkables Shear Zone. Most of the age spectra from within the core of the schist belt yield complex age spectra that we interpret to be the result of prolonged residence within the argon partial retention interval for white mica (430–330 °C). Samples with apparent ages of about 110–109 Ma tend to give concordant plateaux suggesting more rapid cooling. The youngest and most disturbed age spectra come from within the ‘Alpine chlorite overprint’ zone where samples with strong development of crenulation cleavage gave ages 85–107 and 101 Ma, due to partial resetting during retrogression. The bounding Remarkables Shear zone shows resetting effects due to dynamic recrystallization with apparent ages of 127–122 Ma, whereas overprinting shear zones within the core of the schist show apparent ages of 112–109 and 106 Ma. These data when linked with extensional exhumation of high-grade rocks in other parts of New Zealand indicate that the East Gondwana margin underwent significant extension in the 110–90 Ma period.  相似文献   

10.
This study provides information on non-aromatic hydrocarbons contained in thick Palaeogene halite sequences in the Bresse region (France). The presence of almost uniquely biological markers and the absence of thermogenic compounds denote the low maturity of the corresponding samples consistent with Rock-Eval pyrolysis data. The distribution of n-alkanes enables the distinction of three main biological signatures: algal (mode in nC17–nC18); terrestrial (mode in nC29–nC31) and bacterial (mode in nC25–nC26 with no odd-even carbon number predominance). As to the cyclic biomarkers, hopanes and hopenes are largely predominant over steranes and diasterenes in samples having received appreciable amounts of terrestrial inputs (Type B) and conversely for the samples containing high proportions of algal debris (Type A, Type C).  相似文献   

11.
Water samples from 72 wells tapping the Jilh aquifer were collected and analyzed for 10 different water quality parameters. Using these data, a regional irrigation water quality was assessed using three techniques: (i) United States Department of Agriculture method (USDA), (ii) Food and Agriculture Organization (FAO) guidelines for water quality assessment, and (iii) Water-Types approach. The USDA method revealed that the aquifer water salinity, as represented by electrical conductivity, ECw, ranges from high salinity (C3: ECw > 0.75–2.25 dS/m) to a very high salinity (C4: ECw > 2.25 dS/m). The sodium adsorption ratio (SAR) varied from low (S1) to very high (S4) sodicity. Therefore, the water of the Jilh aquifer is dominantly of the C4–S2 class representing 56% of the total wells followed by C4–S1, C4–S3, C3–S1 and C4–S4 classes at 19%, 14%, 8%, and 3% of the wells respectively. The FAO system indicated moderate to severe restriction on the use for irrigation and slight to moderate ion toxicities for Na+, Cl−, B+, NO3− and HCO3−. It is clear that, both USDA and FAO systems condemn the Jilh groundwater as hazardous for irrigation due to its high salt content, unless certain measures for salinity control are undertaken. The dominant salt constituents in the water are Mg–Cl2, Na–Cl and Ca–Cl2 as per the Water-Types method. However, due to the complexity in classifying the aquifer groundwater for irrigation, a simplified approach acknowledging three class groups (I-suitable water, II-conditionally suitable water and III-unsuitable water) adopted from the three methods, is suggested in this paper. The simplified approach combines C–S classes of the USDA method among these three groups according to the lowest ratings. The salinity of the FAO method has been split arbitrarily into slight and moderate subclasses with values of 0.7–2.25 and >2.25 dS/m, respectively; to match with the C3-class of the USDA system. The Water-Types were classified assuming that Ca–Cl2 is the least hazardous salt, followed by Mg–Cl2 and Na–Cl. Using this integrated hydrochemical method, the majority of the wells (92%) contain unsuitable water for irrigation (Group III) while the remaining wells (8%) are in Group II with water considered conditionally suitable for irrigation.  相似文献   

12.
The aim of this work is to study the suitability of the use of fluorescence and UV–visible spectroscopies to evaluate the humification degree of different organic alkaline extracts obtained from diverse materials (humic substances, composted and non-composted materials). Our results indicate that the complementary utilization of the fluorescence index proposed by Milori et al. [Milori, D., Martin-Neto, L., Bayer, C., Mielniczuk, J., Vagnato, V., 2002. Humification degree of soil humic acids determined by fluorescence spectroscopy. Soil Science, 167, 739–749] (the total area of the emission spectra collected over a range of 460–650 nm using an excitation wavelength of 465 nm), the ratio between the electron-transfer band and benzenoid band of benzene UV light absorption, and the molar absorption coefficients at 600 nm and 280 nm proved capable of discriminating between extracts obtained from non-humified, partially humified and very humified materials.Likewise, our results suggest that humification is related to increments in the aromatic character of the molecules, which may be reflected in the presence of more aromatic rings and/or more condensed polyaromatic structures, and the degree of substitution in aromatic rings with polar functional groups, as well as to the possible increase in the conjugation degree in unsaturated aliphatic chains.  相似文献   

13.
Palaeoenvironmental studies combining 14C dating, palaeobotanical and archaeological data provide information about the human reaction to Holocene environmental changes registered in the surroundings of Biržulis Lake in northwest Lithuania.Responding to water regression, early Mesolithic communities were established on the lower lake terraces, which were overgrown by predominantly birch and pine forest. The formation of a mixed forest with Ulmus (immigrated at 8100–7500 cal yr BC), Corylus (7600–7200 cal yr BC) and Alnus (7300–6900 cal yr BC) provided plenty of natural resources, which led to the increase in population during the late Mesolithic. The expansion of Tilia (6400–5900 cal yr BC) and Quercus (5900–5700 cal yr BC), as well as the subsequent flourishing of broad-leaved forest, provided inhabitants with suitable living conditions.The reduction of broad-leaved woodland and the expansion of Picea (4400–3700 cal yr BC), which suggest changing temperature and moisture conditions as well as increasing erosion activity, could have negatively influenced the early-middle Neolithic population, as evidenced by the partial abandoning of the land. The lowering of the water level and thinning of the forest structure possibly related to some dry episode, positively influenced late Neolithic groups, as intensive exploitation of the area, including the earliest attempts at agriculture, has been registered. Since 1770–1490 cal yr BC, when intensive bogging began, evidence of periodic inhabitation around the lake has been registered.  相似文献   

14.
This study examined the dissolved organic matter (DOM) components of cow dung using a combination of fluorescence (excitation–emission matrix, EEM) spectroscopy and parallel factor (PARAFAC) modelling along with eleven trace metals using ICP-MS and nutrients (NH4+ and NO3?) using an AA3 auto analyser. EEM–PARAFAC analysis demonstrated that cow dung predominantly contained only one fluorescent DOM component with two fluorescence peaks (Ex/Em = 275/311 nm and Ex/Em = 220/311 nm), which could be denoted as tyrosine by comparison with its standard. Occurrence of tyrosine can be further confirmed by the FTIR spectra. Trace metals analysis revealed that Na, K and Mg were significantly higher than Ca, Fe, Mn, Zn Sr, Cu, Ni and Co. The NH4+ concentrations were substantially higher than NO3?. These results thus indicate that the dissolved components of the cow dung could be useful for better understanding its future uses in various important purposes.  相似文献   

15.
In this study, biometric and structural engineering tool have been used to examine a possible relationship within Chuaria–Tawuia complex and micro-FTIR (Fourier Transform Infrared Spectroscopy) analyses to understand the biological affinity of Chuaria circularis Walcott, collected from the Mesoproterozoic Suket Shales of the Vindhyan Supergroup and the Neoproterozoic Halkal Shales of the Bhima Group of peninsular India. Biometric analyses of well preserved carbonized specimens show wide variation in morphology and uni-modal distribution. We believe and demonstrate to a reasonable extent that C. circularis most likely was a part of Tawuia-like cylindrical body of algal origin. Specimens with notch/cleft and overlapping preservation, mostly recorded in the size range of 3–5 mm, are of special interest. Five different models proposed earlier on the life cycle of C. circularis are discussed. A new model, termed as ‘Hybrid model’ based on present multidisciplinary study assessing cylindrical and spherical shapes suggesting variable cell wall strength and algal affinity is proposed. This model discusses and demonstrates varied geometrical morphologies assumed by Chuaria and Tawuia, and also shows the inter-relationship of Chuaria–Tawuia complex.Structural engineering tool (thin walled pressure vessel theory) was applied to investigate the implications of possible geometrical shapes (sphere and cylinder), membrane (cell wall) stresses and ambient pressure environment on morphologically similar C. circularis and Tawuia. The results suggest that membrane stresses developed on the structures similar to Chuaria–Tawuia complex were directly proportional to radius and inversely proportional to the thickness in both cases. In case of hollow cylindrical structure, the membrane stresses in circumferential direction (hoop stress) are twice of the longitudinal direction indicating that rupture or fragmentation in the body of Tawuia would have occurred due to hoop stress. It appears that notches and discontinuities seen in some of the specimens of Chuaria may be related to rupture suggesting their possible location in 3D Chuaria.The micro-FTIR spectra of C. circularis are characterized by both aliphatic and aromatic absorption bands. The aliphaticity is indicated by prominent alkyl group bands between 2800–3000 and 1300–1500 cm−1. The prominent absorption signals at 700–900 cm−1 (peaking at 875 and 860 cm−1) are due to aromatic CH out of plane deformation. A narrow, strong band is centred at 1540 cm−1 which could be COOH band. The presence of strong aliphatic bands in FTIR spectra suggests that the biogeopolymer of C. circularis is of aliphatic nature. The wall chemistry indicates the presence of ‘algaenan’—a biopolymer of algae.  相似文献   

16.
A polymetamorphic complex in the Arunta Block, Central Australia, which has undergone metasomatism involving introduction of Rb and loss of Sr has been investigated by 40Ar/ 39Ar step and total-degassing techniques in an attempt to date five metamorphic events (M1–M5) identified microstructurally. The complex isotopic data and apparent age spectra obtained have been interpreted in the light of constraints provided by an associated tectonometamorphic study, together with independent geochronological controls from the immediate study area and elsewhere in the Arunta Block. This has led to the delineation of ages of 1,780–1,820 M.y. for M1, 1,690–1,720 M.y. for M2, 1,450–1,500 M.y. for M3, 1,030–1,060 M.y. for M4 and 370–510 for M5. The polyphase M5 event is correlated with the Alice Springs Orogeny, previously accorded younger age limits of 330–370 M.y. The latter are interpreted to reflect closure of mica K/Ar systems as uplift continued subsequent to the close of the event, possibly culminating in minor high-level brittle deformation and the development of pseudotachylytes in the study area.Apparent age spectra recorded in this study do not all conform with generally accepted patterns of behaviour of mineral systems which have undergone polythermal histories. Two hornblendes have survived subsequent high temperature metasomatic reheating without loss of argon or resetting of their ages. Their resistance to argon loss may be attributable to low water contents, due to their growth under anhydrous granulite facies conditions, and may reflect a relationship between argon loss from hornblende and the water content of hornblende, which decreases with increasing metamorphic grade (Kostyuk and Sobolev 1969). Other samples display false plateaux in their apparent age spectra and in three cases the spectra are indistinguishable from those of undisturbed spectra.The age data recorded in this study suggest that during basement reactivation loss of argon is mainly confined to the vicinity of shear zones, implying that diffusion of argon from minerals in the deep crust may be dependent more on deformation than on reheating. However, thermal activity may also be associated with active shear zones, through the medium of superheated fluids streaming up the shear zones from below. The wide spread of K/Ar and 40Ar/39Ar ages (330–510 M.y.), recorded for the Alice Springs Orogeny in the Arunta basement, may reflect such controls.  相似文献   

17.
John Wakabayashi   《Tectonophysics》2004,392(1-4):193
Metamorphic pressure (P)–temperature (T) paths are commonly used as tools to interpret the tectonic history of orogenic belts, those deformed belts of rocks that record past activity along active plate margins. Many studies and reviews relating P–T path development to tectonics have focused on thrusting–thermal relaxation cycles, with special emphasis on collisional processes. Other studies have assumed that P–T paths resulted from a single tectono-metamorphic event that accounted for the entire burial–exhumation history of the rocks. In many cases, such assumptions may prove invalid.This paper speculates on the relationship of tectonic processes other than thrusting–heating to P–T path development. The processes discussed herein include subduction initiation, triple-junction interactions, initiation and shut off of arc volcanism, subcontinental delamination, and hot spot migration. All of these processes may leave a signature in the metamorphic rock record. Examples are presented from a number of localities, most of which are from the Pacific Rim. Although thrusting–heating cycles have influenced metamorphic evolution in many orogenic belts, the potential impact of other types of tectonic mechanisms should not be overlooked.  相似文献   

18.
We have obtained high quality Raman spectra for two H/D isotopically substituted hydrous aluminosilicate glasses with compositions along the NaAlSi3O8-SiO2 join. Consistent with the results of previous studies, the isotope shift for the band near 900 cm–1, whose intensity grows with increasing water content, is extremely small: v h /v d = 1.004 ± 0.004. The lack of a definite H/D isotope shift for this band does not, however, preclude its association with a vibration of a hydrous species in the glass, because of likely strong coupling between different vibrational modes of hydrated framework species. The 900 cm–1 band could well be due to a T — OH (T = Si, Al) stretching or bending vibration in the hydrous glass, as required by the presence of a combination band near 4500 cm–1 in near-infrared spectra.  相似文献   

19.
Temperature and H2O activity can be determined with high precision using metamorphic mineral assemblages that define both a dehydration equilibrium and a temperature-sensitive cation-exchange equilibrium. Such determinations are obtained by applying the Gibbs method and then integrating two resulting differential equations, as illustrated here for the assemblage garnet-chlorite-quartz. The first equation, a geothermometer that monitors temperature based upon Fe–Mg exchange between garnet and chlorite, was calibrated using rocks at Pecos Baldy, New Mexico: 0=0.05 P(bars)–19.02 T(K)+4607 ln K D+24,156 with errors of ±8°C based upon analytical precision. The second equation monitors differences in the activity of water between specimens (1) and (2): 0=(0.1 X Mg–chl, 1 – 2.05)(P 2 – P 1) +[–33.02+5.96 ln(X Fe–chl, 1/X alm, 1)][T 2–T 1 –2.67 RT 1ln[a(H2O)2/a(H2O)1] +5.96 T 1ln(X Fe–chl, 2 X alm, 1/X Fe–chl, 1 X alm, 2).For samples equilibrated at the same pressure and temperature, microprobe analytical errors of 1% limit precision to ±0.01 a(H2O). For samples equilibrated at the same pressure but variable temperature, uncertainty of ±8°C limits precision to ±0.06 a(H2O). Extreme presure sensitivity requires that the H2O-barometer be applied only to rocks where pressure gradients are absent or well-constrained. The geothermometer gives temperatures in agreement with two other garnet-chlorite geothermometers (Dickenson and Hewitt 1986; Ghent et al. 1987) and with garnet-biotite geothermometry (ferry and Spear 1978) over the temperature range 350–520°C. Application of the relative H2O barometer shows variations in the activity of water approaching 0.30 in several study areas. Either pelitic schists commonly equilibrate with a fluid that is not pure H2O, or some pelitic rocks undergo metamorphism in the absence of a free fluid phase.  相似文献   

20.
Particulate matter and interfacial sediment from a seasonally anoxic coastal salt pond were analyzed for fatty acids and sterols to examine variations in organic sources, and compositional changes across the oxic-anoxic interface in the water column and at the sediment-water interface. Fatty acid distributions in suspended particles varied seasonally and as a function of depth. Fatty acids of algal origin (e.g. 16:3, 16:4, 18:3, 18:4) were abundant in particles in oxic surface waters, but these labile components were depleted in particles from the anoxic zone which instead were enriched in bacterial fatty acids (e.g. 16:1Δ9, 18:1Δ11, anteiso-C15). Sterol distributionsvaried less than fatty acid distributions and particles throughout the water column reflected an upper water algal source with little in situ alteration. There was evidence for an in situ conversion of Δ5-stenols to 5(α)H-stanols in suspended particles in the anoxic zone. Sinking particles and the interfacial sediment were compositionally similar to each other, but different from suspended particles. These data reflect differences in particle source, transport and transformation processes occuring in the water column.  相似文献   

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