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1.
Although the bulk moduli (KT0) of silicate melts have a relatively narrow range of values, the pressure derivatives of the isothermal bulk modulus (KT0′) can assume a broad range of values and have an important influence on the compositional dependence of the melt compressibility at high pressure. Based on the melt density data from sink/float experiments at high pressures in the literature, we calculate KT0′ using an isothermal equation of state (EOS) (e.g., Birch–Murnaghan EOS and Vinet EOS) with the previously determined values of room-pressure density (ρ0) and room-pressure bulk modulus (KT0). The results show that best estimates of KT0′ vary considerably from ~ 3 to ~ 7 for different compositions. KT0′ is nearly independent of Mg # (molar Mg/(Mg + Fe)), but decreases with SiO2 content. Hydrous melts have anomalously small KT0′ leading to a high degree of compression at high pressures. For anhydrous melts, KT0′ is ~ 7 for peridotitic melts, ~ 6 for picritic melts, ~ 5 for komatiitic melts, and ~ 4 for basaltic melts.  相似文献   

2.
Gas concentrations and isotopic compositions of water have been measured in hydrothermal waters from 13°N on the East Pacific Rise. In the most Mg-depleted samples ( 5 × 10−3 moles/kg) the gas concentrations are: 3–4.5 × 10−5 cm3 STP/kg helium, 0.62–1.24 cm3 STP/kg CH4, 10.80–16.71 × 10−3 moles/kg CO2. The samples contain large quantities (95–126 cm3/kg) of H2 and some carbon monoxide (0.26–0.36 cm3/kg) which result from reaction with the titanium sampling bottles. δ13C in methane and CO2 (−16.6 to −19.5 and −4.1 to −5.5 respectively) indicate temperatures between 475 and 550°C, whereas δ13CCO is compatible with formation by reduction of CO2 on Ti at 350°C close to the sampling temperature.3He/4He are very homogeneous at (7.5 ± 0.1)RA(3He/4He = 1.0 × 10−5) and very similar to already published data as well as CH4/3He ratios between 1.4 and 2.1 × 106.18O and D in water show enrichments from 0.39 to 0.69‰ and from 0.62 to 1.49‰ respectively. These values correspond to W/R ratios of 0.4–7. The distinct18O enrichments indicate that the isotopic composition of the oceans is not completely buffered by the hydrothermal circulations. The3He-enthalpy relationship is discussed in terms of both hydrothermal heat flux and3He mantle flux.  相似文献   

3.
The precise knowledge of the initial 26Al/27Al ratio [(26Al/27Al)0] is crucial if we are to use the very first solid objects formed in our Solar System, calcium–aluminum-rich inclusions (CAIs) as the “time zero” age-anchor and guide future work with other short-lived radio-chronometers in the early Solar System, as well as determining the inventory of heat budgets from radioactivities for early planetary differentiation. New high-precision multi-collector inductively-coupled plasma mass spectrometry (MC-ICP-MS) measurements of 27Al/24Mg ratios and Mg-isotopic compositions of nine whole-rock CAIs (six mineralogically characterized fragments and three micro-drilled inclusions) from the CV carbonaceous chondrite, Allende yield a well-defined 26Al–26Mg fossil isochron with an (26Al/27Al)0 of (5.23 ± 0.13) × 10− 5. Internal mineral isochrons obtained for three of these CAIs (A44A, AJEF, and A43) are consistent with the whole-rock CAI isochron. The mineral isochron of AJEF with (26Al/27Al)0 = (4.96 ± 0.25) × 10− 5, anchored to our precisely determined absolute 207Pb–206Pb age of 4567.60 ± 0.36 Ma for the same mineral separates, reinstate the “canonical” (26Al/27Al)0 of 5 × 10− 5 for the early Solar System. The uncertainty in (26Al/27Al)0 corresponds to a maximum time span of ± 20 Ka (thousand years), suggesting that the Allende CAI formation events were culminated within this time span. Although all Allende CAIs studied experienced multistage formation history, including melting and evaporation in the solar nebula and post-crystallization alteration likely on the asteroidal parent body, the 26Al–26Mg and U–Pb-isotopic systematics of the mineral separates and bulk CAIs behaved largely as closed-system since their formation. Our data do not support the “supra-canonical” 26Al/27Al ratio of individual minerals or their mixtures in CV CAIs, suggesting that the supra-canonical 26Al/27Al ratio in the CV CAIs may have resulted from post-crystallization inter-mineral redistribution of Mg isotopes within an individual inclusion. This redistribution must be volumetrically minor in order to satisfy the mass balance of the precisely defined bulk CAI and bulk mineral data obtained by MC-ICP-MS.The radiogenic 208Pb/206Pb ratio obtained as a by-product from the Pb–Pb age dating is used to estimate time-integrated 232Th/238U ratio (κ value) of CAIs. Limited κ variations among the minerals within a single CAI, contrasted by much larger variations among the bulk CAIs, suggest Th/U fractionation occurred prior to crystallization of igneous CAIs. If interpreted as primordial heterogeneity, the κ value can be used to calculate the mean age of the interstellar dust from which the CAIs condensed.  相似文献   

4.
We assessed leaf breakdown of five native riparian species from Brazilian Cerrado (Myrcia guyanensis, Ocotea sp., Miconia chartacea, Protium brasiliense, and Protium heptaphyllum), incubated in single and mixed species packs in two headwater streams with different physico-chemical properties in the Espinhaço Mountain range (Southeastern Brazil). Leaves were placed in plastic litter bags (15 cm×20 cm, 10 mm mesh size) and the experiments were carried out during the dry seasons of 2003 and 2004. Leaf nitrogen and phosphorus contents were similar in all species, but polyphenolic contents were different (P<0.001). M. guyanensis showed higher polyphenolics content (8.48% g−1 dry mass) and leaf toughness. Individually, higher breakdown rates were found in M. guyanensis at Indaiá stream (k=0.0063±0.0005 d−1) and in Ocotea sp. at Garcia stream (k=0.0088±0.0006 d−1). However, P. brasiliense and P. heptaphyllum showed lower breakdown rates at Indaiá and Garcia streams (Indaiá: k=0.0020±0.0002 and 0.0019±0.0001 d−1; Garcia: k=0.0042±0.0001 and 0.0040±0.0002 d−1). Single and mixed breakdown processes of each species were not statistically different on both streams. However, all species showed higher breakdown rates at Garcia stream (P<0.01). These results suggest that leaf breakdown is not altered when litter benthic patches are composed by a mixture of species in the same proportions that they occur on riparian leaf falls.  相似文献   

5.
Oxygen self diffusion rates were determined in quartz samples exchanged with18O-enriched CO2 between 745 and 900°C and various pressures, and the diffusion profiles were measured using an ion microprobe. The activation energy (Q) and preexponential factor (D0) at P(CO2) = P(tot) = 100 bar, for diffusion parallel to the c-axis are 159 ( ± 13) kJ/g atom and 2.10 (+0.75/ −0.55) × 10−8 cm2/s. This rate is approximately 100 times slower than that obtained from hydrothermal experiments and 100 times faster than a previous 1-bar quartz-O2 exchange experiment. The oxygen diffusion rate measured at 0.6 bar, 888°C, and at 900°C in vacuum is in agreement with the previous 1-bar exchange experiments with18O2. The effect of higher CO2 pressures is small. At 900°C, the diffusion rate exchanged with CO2 is = 2.35 × 10−15 cm2/s at 100 bar, 2.24 × 10−15 cm2/s at 3.45 kbar and 8.13 × 10−15 cm2/s at 7.2 kbar.There is probably a diffusing species, other than oxygen, that enhances the oxygen diffusion rate in these quartz-CO2 systems, relative to that occurring at very low pressures or in a vacuum. The effect of this diffusing species, however, is not as strong as that associated with H2O. Preserved oxygen isotope fractionations between coexisting minerals in a slowly cooled, high-grade metamorphic terrane will vary depending upon whether a water-rich phase was present or not. Closure temperatures will be approximately 100°C higher in rocks where no water-rich phase was present during cooling. The measured fractionations between coexisting minerals in metamorphic rocks may potentially be used as a sensor of water presence during retrogression.  相似文献   

6.
Beryllium isotopes (10Be and9Be) have been measured in suspended particles of < 1 mm size collected by mid-water sediment traps deployed in the eastern Pacific at MANOP sites H (6°32′N, 92°50′W, water depth 3600 m) and M (8°50′N, 104°00′W, 3100 m). For comparison, surface sediments from box cores taken from the two sites were also studied. The concentrations of10Be and9Be in sediment-trap particles are about an order of magnitude smaller than those in the bottom sediments which contain about 8 × 109 and 6 × 1016 atoms g−1 of10Be and9Be, respectively. The sediment trap samples collected from 50 m off the bottom showed significant (26–63%) contributions from resuspended bottom sediments. The10Be/9Be ratio in trap samples varies from 3 to 20 × 10−8. The variation may partly result from varied proportion of authigenic/detrital material. The fluxes of both isotopes exhibit a very strong seasonality. The fluxes of10Be into the traps at about 1500 m are estimated as 9 × 105 and 4 × 105 atoms cm−2 a−1 at sites H and M respectively. These values are to be compared with the fluxes into the sediments of 4–5 × 105 atoms cm−2 a−1 at both locations. Good correlations exist between10Be,9Be and27Al indicating that the primary carrier phase(s) for the beryllium isotopes in the water column may be aluminosilicates.  相似文献   

7.
LaCe ages are reported for two sets of Finnish pegmatites, Lövböle and Mustikkamäki, and for an Amiˆtsoq gneiss, Greenland. When λβ138La value (2.29 × 10−12 yr−1) obtained by radioactivity measurement [1] is used for the chronological calculation, the LaCe ages (2129, 2325, 3271 Myr) evaluated for these rocks are 18–35% older than the SmNd ages for the same samples. To make the LaCe age fit to the SmNd age for the same sample, a new value of (2.77 ± 0.21) × 10−12 yr−1 is evaluated for λβ138La. In this calculation, the LaCe and SmNd ages reported for a Bushveld gabbro [2] have been also taken into account together with those for the Lövböle pegmatite and the Mustikkamäki pegmatite, while the Amiˆtsoq gneiss (GGU110999) has been omitted because of the complicated thermal history of this sample.  相似文献   

8.
The Laccadive Ridge (L-R), trending roughly parallel to the west coast of India, is an intriguing segment of the northernmost Chagos-Laccadive Ridge (C-L-R) system. Although crustal nature and isostatic response of the southern C-L-R is well known, there are no similar studies on the L-R. In the present study, the isostatic response of the lithosphere beneath the L-R is estimated so as to characterize its crustal nature, total crustal as well as effective elastic plate thickness and mode of compensation. Twelve gravity and bathymetry profiles across the ridge were analyzed using linear transfer function and forward model techniques. The observed admittance function within the diagnostic waveband of 250 < λ > 80 km (0.025 < k > 0.080 km−1) fits well with (i) the Airy model whose average crustal thickness (Tc) and density are 17 ± 2 km and 2.7 × 103 kg m−3, respectively, and (ii) the thin plate flexure model of isostasy with an effective elastic plate thickness (Te) of 2–3 km. The estimated average crustal thickness and density are in good agreement with published seismic refraction results over the ridge. The results of the present study support an Airy model of isostasy for the L-R. The low Te value, in view of other published results in the study area, suggests stretched and loaded continental lithosphere of the L-R during the evolution of the western continental margin of India.  相似文献   

9.
In order to better constrain the extent to which common sulfide minerals will retain their osmium isotopic composition subsequent to crystallization, we have conducted experiments to quantify the diffusion behavior of osmium in pyrite and pyrrhotite. Experiments consisted of either (1) isothermal soaking of diffusion couples consisting of natural pyrite or pyrrhotite crystals packed against powdered Os-bearing Fe-sulfide or (2) ‘relaxation’ of initially high near-surface osmium concentrations produced in the latter experiments (pyrite only). Osmium penetration into samples was characterized by depth profiling using Rutherford backscattering spectroscopy (RBS) (pyrite) or electron microprobe analyses across sectioned run products (pyrrhotite). Results of the first type of diffusion experiment involving pyrite show only limited osmium penetration into sample surfaces, with the extent of penetration uncorrelated with run duration. Images of pyrite samples using atomic force microscopy show roughening of initially smooth surfaces as a consequence of step formation and suggest that osmium incorporation into the near-surface occurred by solute uptake during step growth and not by volume diffusion. Prolonged (1000+ h) ‘relaxation’ experiments revealed no additional osmium penetration into pyrite surfaces and based on the depth resolution for RBS, a maximum diffusion coefficient of 2.5×10−23 m2/s at 500°C was calculated. Experiments involving pyrrhotite over the temperature range of 950–1100°C showed extensive osmium uptake and osmium concentration gradients that conform with Fickian diffusion behavior. We found that pyrrhotite Fe/S could be varied by changes in the composition of the starting material and osmium source and over the range of Fe/S produced in experiments (molar Fe/S=0.83–0.90), we observed no systematic variation in the osmium diffusion coefficient. Diffusion coefficients measured parallel to the a crystallographic axis were on average 1.4× higher than values measured parallel to c and regression of the c-axis data yielded the Arrhenius relation:
The application of these diffusion data to simple models of diffusive exchange during static or polythermal time–temperature histories is used to assess the conditions under which radiogenic osmium will be retained. During isothermal annealing, calculations indicate that the cores of millimeter-sized spherical pyrrhotite crystals undergoing diffusive exchange with an external osmium reservoir will have their initial compositions perturbed in ≤0.5 Ma at temperatures exceeding 400°C. Pyrite undergoing the same process at 500°C requires in excess of 10 Ma before crystal cores are affected. The relatively short ‘core retention’ time-scales for pyrrhotite indicates that this mineral may be prone to isotopic resetting following relatively brief crustal thermal events, thus possibly accounting for the scatter that commonly occurs in Re–Os isochrons generated from massive sulfide samples. Calculated closure temperatures (Tc) for osmium exchange in pyrrhotite yielded values of 300–400°C for grain sizes ranging from 10 to 1000 μm. These values of Tc are similar to those calculated for Ar retention in biotite, and considerably lower than for Sr in apatite and plagioclase, for example. Such low closure temperatures for pyrrhotite suggest this mineral will date the final stage in the cooling of a magmatic system and possibly be susceptible to open system osmium exchange in the presence of late-stage hydrothermal fluids. This latter result infers that caution be applied when interpreting elevated initial osmium isotopic ratios as a product of crustal assimilation at the magmatic stage.  相似文献   

10.
The hemolytic activity of the dinoflagellate Cochlodinium polykrikoides from Bahía de La Paz, Gulf of California was investigated as part of the ichthyotoxic mechanism of this microalga. Two different kinds of erythrocytes, fish and human, were tested for the hemolytic assay. Since fatty acids have been associated with hemolytic activity in C. polykrikoides, the composition of fatty acids of this dinoflagellate was also analyzed. The concentration of C. polykrikoides causing 50% hemolysis (HE50) was 4.88 and 5.27 × 106 cells L−1, for fish and human erythrocytes, respectively. According to the standard curve of saponin, an equivalence between the hemolytic activity of saponin and the dinoflagellate concentration was found with 1 μg saponin mL−1 equivalent to 1 × 106 cells L−1 of C. polykrikoides. The polyunsaturated fatty acids: hexadecaenoic (16:0), docosahexaenoic (22:6 n3) and octadecapentaenoic (18:5 n3) were found in an abundance of 62% of total fatty acids.  相似文献   

11.
A series of experiments and petrographic analyses have been run to determine the pre-eruption phase equilibria and ascent dynamics of dacitic lavas composing Black Butte, a dome complex on the flank of Mount Shasta, California. Major and trace element analyses indicate that the Black Butte magma shared a common parent with contemporaneously erupted magmas at the Shasta summit. The Black Butte lava phenocryst phase assemblage (20 v.%) consists of amphibole, plagioclase (core An77.5), and Fe–Ti oxides in a fine-grained (< 0.5 mm) groundmass of plagioclase, pyroxene, Fe–Ti oxides, amphibole, and cristobalite. The phenocryst assemblage and crystal compositions are reproduced experimentally between 890 °C and 910 °C, ≥ 300 MPa, XH2O = 1, and oxygen fugacity = NNO + 1. This study has quantified the extent of three crystallization processes occurring in the Black Butte dacite that can be used to discern ascent processes. Magma ascent rate was quantified using the widths of amphibole breakdown rims in natural samples, using an experimental calibration of rim development in a similar magma at relevant conditions. The majority of rims are 34 ± 10 μm thick, suggesting a time-integrated magma ascent rate of 0.004–0.006 m/s among all four dome lobes. This is comparable to values for effusive samples from the 1980 Mount St. Helens eruption and slightly faster than those estimated at Montserrat. A gap between the compositions of plagioclase phenocryst cores and microlites suggests that while phenocryst growth was continuous throughout ascent, microlite formation did not occur until significantly into ascent. The duration of crystallization is estimated using the magma reservoir depth and ascent rate, as determined from phase equilibria and amphibole rim widths, respectively. Textural analysis of the natural plagioclase crystals yields maximum growth rates of plagioclase phenocryst rims and groundmass microlites of 8.7 × 10− 8 and 2.5 × 10− 8 mm/s, respectively. These rates are comparable to values determined from time-sequenced samples of dacite erupted effusively from Mount St. Helens during 1980 and indicate that syneruptive crystallization processes were important during the Black Butte eruptive cycle.  相似文献   

12.
Windsor–Essex County is a major cross-border truck and transportation route, with significant localized industrialization as well as rural and farming areas. Magnetic property measurements (in-field and laboratory susceptibility, frequency-dependent susceptibility, hysteresis properties, thermomagnetic and thermosusceptibility curves, anhysteretic and isothermal magnetizations) were made in order to determine the potential for using such variables to distinguish between natural and anthropogenic pollutants. In-field magnetic susceptibility measured on 324 soil sampling sites on a 0.5–2 km grid spacing through Windsor–Essex County ranged from 3.7 × 10− 6 to 305.2 × 10− 6 SI (average 36.2 ± 35.8 × 10− 6 SI), and showed that high magnetic susceptibility values were obtained on soil sampling sites in and around the cities/towns of Windsor, Harrow, Olinda and Oakland and near the beaches of Point Pelee National Park (PPNP) and Deerbrook, whereas lower susceptibility values were observed in near the towns of Lakeshore and Essex. On this grid spacing, Highway 401 (the major truck route) did not show anomalous susceptibility values; however, closer (1–3 m) sampling on other roads did show anomalously high values, suggesting that the coarser grid spacing may have missed anomalies. Laboratory measurements indicated that the dominant magnetic mineral in the Windsor–Essex County soils is magnetite; however, the grain size is variable. Pseudo-single domain (PSD)–multidomain (MD) magnetite is generally found on beaches and in PPNP, whereas single domain (SD)–PSD magnetite has been found near the City of Windsor and other towns. While certain correlations exist between some anthropogenic activities and the measured magnetic susceptibility and magnetic property values, no overall correlation can be made. A variety of geologic and anthropogenic factors must be considered when interpreting the origin of the magnetic signal in a particular area.  相似文献   

13.
We analyze observations from eight GPS campaigns carried out between 1997 and 2005 on a network of 13 sites in the Suez–Sinai area, where separation between the African and the Arabian plates takes place. This is the key area to understand if and in which way Sinai behaves like a sub-plate of the African plate and the role played by seismic and geodetic (long-term) deformation release.Our analysis shows that, on average, the Suez–Sinai area motion, in terms of ITRF00 velocities, matches the African plate motion defined by the NNR-NUVEL-1A model.The horizontal principal strain rate axes estimated separately in the Gulf of Suez area and in the northern Sinai vary from compression across the Gulf (−2.2 ± 1.2) × 10−8 year−1 to NE extension (1.0 ± 1.5) × 10−8 year−1 in the North, showing the presence of two distinct domains, so that in our opinion Sinai cannot be considered simply a unique rigid block.The analysis of GPS baseline length variations shows short-term deformations across the Gulf of Suez, reaching up a maximum value of more than 1 cm in 8 years.Since current geodynamical models do not predict significant tectonic deformation in this area, we work under the hypothesis that a contribute may be expected by post-seismic relaxation effects. Under this hypothesis, we compare the baselines length variations with the post-seismic relaxation field associated with five major local earthquakes occurred in the area, testing two different viscoelastic models. Our results show that the detected short-term deformations are better modeled for viscosity values of 1018 Pa s in the lower crust and 1020 Pa s in the asthenosphere. However, since the modeled post-seismic effect results modest and a certain amount of the detected deformation is not accounted for, we think that an improved modeling should take into account the lateral heterogeneities of crust and upper mantle structures.  相似文献   

14.
The viscosity of a natural phonolitic composition with variable amounts of H2O has been experimentally determined. The starting materials were crystal-free phonolitic glasses from Montaña Blanca, situated within the Las Cañadas caldera of Teide. Dry phonolitic melt viscosities were determined using concentric cylinder viscometry in the low viscosity range. The glassy quench products of these runs were then hydrated by high pressure synthesis in a piston–cylinder apparatus to generate a suite of samples with water contents ranging from 0.02 to 3.75 wt%. Samples thus hydrated were quenched rapidly and prepared (cut and polished) for the determination of water contents by infrared spectroscopy before and after experimental viscometry. The viscosities of the melts (dry and hydrated) were determined at 1 bar using a micropenetration technique. Samples were stable under the measurement conditions up to 3.75 wt% H2O. Homogeneity of water content was confirmed by infrared spectroscopy and total water contents were calculated using absorptivity coefficients for compositions extremely close to that investigated here. The variation of viscosity as a function of water content and temperature can be described in the high viscosity interval of relevance to many welding processes by the non-Arrhenian expression:
(1)
log10 η=−5.900−0.286 ln (H2O)+(10775.4−394.8(H2O))/(T−148.7+21.65 ln (H2O))
whereas the high viscosity range alone is adequately described by the Arrhenian expression
(2)
log10 η=−10.622−0.738 ln (H2O)+(17114.3−590.4(H2O))×1/T
where η is the viscosity in Pa s, H2O is the water content in wt% and T is the temperature in K.These results are particularly useful for the scaling of conditions extant during the welding of phonolitic products of Montaña Blanca. The welding of glassy phonolitic rocks is enhanced by the lower viscosity of these melts with respect to calcalkaline rhyolites. The ratio of viscosities of phonolitic to calcalkaline rhyolitic melts is a complex function of temperature and water content and reaches up to 104.5 at 0.1 wt% H2O and 500°C. Abundant evidence of welding and remobilisation of pyroclastic and spatter products of Teide system volcanism are consistent with these experimental observations.  相似文献   

15.
Sulfur isotope effects during the SO2 disproportionation reaction to form elemental sulfur (3SO2+3H2O→2HSO4−+S+2H+) at 200–330°C and saturated water vapor pressures were experimentally determined. Initially, a large kinetic isotopic fractionation takes place between HSO4− and S, followed by a slow approach to equilibrium. The equilibrium fractionation factors, estimated from the longest run results, are expressed by 1000 ln αHSO4−–S=6.21×106/T2+3.62. The rates at which the initial kinetic fractionation factors approach the equilibrium ones were evaluated at the experimental conditions.δ34S values of HSO4− and elemental sulfur were examined for active crater lakes including Noboribetsu and Niseko, (Hokkaido, Japan), Khloridnoe, Bannoe and Maly Semiachik (Kamchatka), Poás (Costa Rica), Ruapehu (New Zealand) and Kawah Ijen and Keli Mutu (Indonesia). ΔHSO4−–S values are 28‰ for Keli Mutu, 26‰ for Kawah Ijen, 24‰ for Ruapehu, 23‰ for Poás, 22‰ for Maly Semiachik, 21‰ for Yugama, 13‰ for Bannoe, 9‰ for Niseko, 4‰ for Khloridonoe, and 0‰ for Noboribetsu, in the decreasing order. The SO2 disproportionation reaction in the magmatic hydrothermal system below crater lakes where magmatic gases condense is responsible for high ΔHSO4−–S values, whereas contribution of HSO4− produced through bacterial oxidation of reduced sulfur becomes progressively dominant for lakes with lower ΔHSO4−–S values. Currently, Noboribetsu crater lake contains no HSO4− of magmatic origin. A 40-year period observation of δ34SHSO4− and δ34SS values at Yugama indicated that the isotopic variations reflect changes in the supply rate of SO2 to the magmatic hydrothermal system. This implies a possibility of volcano monitoring by continuous observation of δ34SHSO4− values. The δ18O values of HSO4− and lake water from the studied lakes covary, indicating oxygen isotopic equilibration between them. The covariance gives strong evidence that lake water circulates through the sublimnic zone at temperatures of 140±30°C.  相似文献   

16.
The vertical distributions of10Be and9Be at three locations in the Pacific (25°N, 170°E; 17°N, 118°W; 3°S, 117°W) are presented. The results show that both isotopes exhibit nutrient-like profiles. From the surface to the bottom, the increase for10Be is two- to threefold and that for9Be is about fivefold. While the inter-station variations in surface water concentrations may reach a factor of two, deep-water values tend to be much more uniform averaging about 2000 atoms/g for10Be and 30 pM for9Be. A similar situation applies to the10Be/9Be ratio; it varies approximately from 1 to 3 × 10−7 (atom/atom) at shallow depths but tends toward a value close to 1.1 × 10−7 in the deep ocean. The variation of10Be/9Be can be viewed as resulting from the fact that10Be in a given parcel of water consists of two components: recycled and primary. The recycled component is that part of10Be which has reached tracer equilibrium with9Be, as opposed to the primary component which, upon entering the sea from the atmosphere, has yet to equilibrate with9Be through particle cycling and mixing processes. It is estimated that 70% to nearly 100% of10Be at the three stations are being recycled, and the recycled beryllium bears an atomic ratio of10Be/9Be close to 1 × 10−7. The oceanic residence time of Be is of the order of 1000–4000 years, comparable to or slightly longer than the ocean mixing time.  相似文献   

17.
We examined the effects of freshwater flow and light availability on phytoplankton biomass and production along the Louisiana continental shelf in the region characterized by persistent spring–summer stratification and widespread summer hypoxia. Data were collected on 7 cruises from 2005 to 2007, and spatially-averaged estimates of phytoplankton and light variables were calculated for the study area using Voronoi polygon normalization. Shelf-wide phytoplankton production ranged from 0.47 to 1.75 mg C m−2 d−1 across the 7 cruises. Shelf-wide average light attenuation (kd) ranged from 0.19–1.01 m−1 and strongly covaried with freshwater discharge from the Mississippi and Atchafalaya Rivers (R2=0.67). Interestingly, we observed that the euphotic zone (as defined by the 1% light depth) extended well below the pycnocline and to the bottom across much of the shelf. Shelf-wide average chlorophyll a (chl a) concentrations ranged from 1.4 to 5.9 mg m−3 and, similar to kd, covaried with river discharge (R2=0.83). Also, chl a concentrations were significantly higher in plume versus non-plume regions of the shelf. When integrated through the water-column, shelf-wide average chl a ranged from 26.3 to 47.6 mg m−2, but did not covary with river discharge, nor were plume versus non-plume averages statistically different. The high integrated chl a in the non-plume waters resulted from frequent sub-pycnocline chl a maxima. Phytoplankton production rates were highest in the vicinity of the Mississippi River bird's foot delta, but as with integrated chl a were not statistically different in plume versus non-plume waters across the rest of the shelf. Based on the vertical distribution of light and chl a, a substantial fraction of phytoplankton production occurred below the pycnocline, averaging from 25% to 50% among cruises. These results suggest that freshwater and nutrient inputs regulate shelf-wide kd and, consequently, the vertical distribution of primary production. The substantial below-pycnocline primary production we observed has not been previously quantified for this region, but has important implications about the formation and persistence of hypoxia on the Louisiana continental shelf.  相似文献   

18.
Results are presented on scubadiving investigations carried out on thermal manifestations in the area of Panarea (Aeolian Islands). The area investigated falls inside a caldera which extends from the main island to the group of islets located to the northeast. The distribution of the gaseous manifestations is regulated by the NE-SW, NW-SE and N-S regional tectonic directrices, through which the more recent basic magma intruded, giving rise to dikes and pillow lavas. fO2-temperature relation of the gases sampled in the investigated area was calculated to be: logfO2 = 11−24,593/T which indicates that a buffering mechanism acted on the gases as they cooled down during their ascent. The high 3He/4He ratio (6 × 10−6) and the δ13C = −3.2%. (PDB), suggest the presence of a magmatic component in the gas feeding the investigated manifestations. The above relations and the almost constant high He/N2 ratio suggest that all the fumaroles are fed by the same deep hot fluids. On the basis of both the chemical characters of the fluids and the geothermo-barometric data, a deep geothermal body, having a temperature of about 240°C, is recognized. Two other shallower thermal aquifers, with a temperature of 170–210°C, are identified. A circulation pattern of the geothermal fluids is also proposed. On the basis of calculations regarding the convective energy released by the geothermal system of Panarea, and the magmatic mass responsible for the positive gravimetric anomaly of the area, it was estimated that the last volcanic activity took place less then 10,000 years ago.  相似文献   

19.
The 1975 sub-terminal activity was characterised by low effusion rates (0.3–0.5 m3 s−1) and the formation of a compound lava field composed of many thousands of flow units. Several boccas were active simultaneously and effusion rates from individual boccas varied from about 10−4 to 0.25 m3s−1. The morphology of lava flows was determined by effusion rate (E): aa flows with well-developed channels and levees formed when E > 2 × 10−3 m3 s−1, small pahoehoe flows formed when 2 × 10−3 m3 s−1 >E > 5 > 10−4 m3 s−1 and pahoehoe toes formed when E < 5 × 10−4 m3 s−1. There was very little variation with time in the effusion temperature, composition or phenocryst content of the lava.New boccas were commonly formed at the fronts of mature lava flows which had either ceased to flow or were moving slowly. These secondary boccas developed when fluid lava in the interior of mature aa flows either found a weakness in the flow front or was exposed by avalanching of the moving flow front. The resulting release of fluid lava was accompanied by either partial drainage of the mature flow or by the formation of a lava tube in the parent flow. The temperature of the lava forming the new bocca decreased with increasing distance from the source bocca (0.035°C m−1). It is demonstrated from the rate of temperature decrease and from theoretical considerations that many of the Etna lavas still contained a substantial proportion of uncooled material in their interior as they came to rest. The formation of secondary boccas is postulated to be one reason why direct measurements of effusion rates tend, in general, to overestimate the total effusion rates of sub-terminal Etna lava fields.  相似文献   

20.
Water samples were collected from Baffin Bay and surrounding areas in order to evaluate this region as a potential source of Nd from old continental material to Atlantic water. The isotopic data ranged from εNd(0) = −9.0 to −26 with most of the data around εNd(0) = −20 compared with values of North Atlantic Deep Water (NADW) with εNd(0) = −13.5. The concentration of Nd in Baffin Bay waters was as high as 6 × 10−12 g/g compared with 2.5 × 10−12 g/g for NADW. The combination of low εNd and high Nd concentration indicates that Baffin Bay may be a significant source of Nd from very old crustal material. A simple box model was used to evaluate the contribution to the Nd budget of NADW and it was concluded that a substantial fraction of the Nd from ancient crustal sources that is required to maintain the isotopic composition of NADW could be supplied by Baffin Bay outflow.  相似文献   

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