Mid-latitude electron content modelling: The role of interhemispheric coupling     

G.C. Sethia  G.J. Bailey  R.J. Moffett  J.K. Hargreaves 《Planetary and Space Science》1985,33(3):321-332

A modelling study of the electron content of the mid-latitude ionosphere and protonosphere has been carried out for solstice conditions using the mathematical model of Bailey (1983). In the model calculations coupled time-dependent O⁺, H⁺ continuity and momentum equations and O⁺, H⁺ and electron heat balance equations are solved for a magnetic shell extending over both hemispheres. The inclusion of interhemispheric flow of plasma and of heat balance has enabled us to investigate the role of interhemispheric coupling on the electron content and related shape parameters. The computed results are compared with results from slant path observations of the ATS-6 radio beacon made at Lancaster (U.K.) and Boulder, Colorado (U.S.A.).It has been found that the conjugate photoelectron heating has a major effect on the shape of the daily variation of slant slab thickness (τ) and also on the magnitude of the protonospheric content (N_p). Some of the main features of τ are closely related to the sunrise and sunset times in the conjugate ionosphere. Also it is found that night-time increases in total electron content (N_T) and F2 region peak electron density (N_max) in winter are natural consequences of ionization loss at low altitudes causing an enhanced downward flow of plasma from the protonosphere which is coupled to the summer hemisphere. One other important consequence of the coupled protonosphere is that the effects on N_T of the neutral air wind are not much different in winter from those in summer.  相似文献   

A community-wide intercomparison exercise for the determination of dissolved iron in seawater     

Andrew R. Bowie  Eric P. Achterberg  Peter L. Croot  Hein J.W. de Baar  Patrick Laan  James W. Moffett  Simon Ussher  Paul J. Worsfold 《Marine Chemistry》2006

The first large-scale international intercomparison of analytical methods for the determination of dissolved iron in seawater was carried out between October 2000 and December 2002. The exercise was conducted as a rigorously “blind” comparison of 7 analytical techniques by 24 international laboratories. The comparison was based on a large volume (700 L), filtered surface seawater sample collected from the South Atlantic Ocean (the “IRONAGES” sample), which was acidified, mixed and bottled at sea. Two 1-L sample bottles were sent to each participant. Integrity and blindness were achieved by having the experiment designed and carried out by a small team, and overseen by an independent data manager. Storage, homogeneity and time-series stability experiments conducted over 2.5 years showed that inter-bottle variability of the IRONAGES sample was good (< 7%), although there was a decrease in iron concentration in the bottles over time (0.8–0.5 nM) before a stable value was observed. This raises questions over the suitability of sample acidification and storage.  相似文献   

Distributions of dissolved and particulate biogenic thiols in the subartic Pacific Ocean     

Christopher L. Dupont  James. W. Moffett  Robert R. Bidigare  Beth A. Ahner 《Deep Sea Research Part I: Oceanographic Research Papers》2006,53(12):1961-1974

Dissolved and particulate concentrations of the biogenic thiols cysteine (Cys), arginine–cysteine (Arg–Cys), glutamine–cysteine (Gln–Cys), γ-glutamate–cysteine (γ-Glu–Cys) and glutathione (GSH) were measured in the subartic Pacific Ocean in the summer of 2003 using high performance liquid chromatography (HPLC) with precolumn derivatization as reported in previous work. In this study, a preconcentration protocol for the derivatized thiols was utilized to extend detection limits of dissolved thiols to picomolar levels. The measured concentrations of particulate and dissolved thiols were uncoupled, with distinctive depth profiles and large differences in the particulate to dissolved ratios between individual compounds. Glutathione was the most abundant particulate thiol whereas the most abundant dissolved thiol was γ-Glu–Cys, with concentrations as high as 15 nM. Given the relatively small pool of intracellular γ-Glu–Cys and the very low dissolved concentrations of GSH, we hypothesize that glutathione released from cells is rapidly converted to the potentially degradation resistant γ-Glu–Cys outside the cell. The relatively high concentrations of other dissolved thiols compared to particulate concentrations implies both biological exudation and slow degradation rates. Some thiols appear to vary with changes in nutrient availability but this effect is difficult to decouple from changes in community structure inferred from pigment analyses. Dissolved thiol concentrations also exceed typical metal concentrations in the subartic Pacific, supporting previous arguments that they may be important in metal speciation.  相似文献   

Thermodynamic characterization of the partitioning of iron between soluble and colloidal species in the Atlantic Ocean   总被引：2，自引：1，他引：2  

Jay T. Cullen  Bridget A. Bergquist  James W. Moffett 《Marine Chemistry》2006,98(2-4):295-303

Recent electrochemical measurements have shown that iron (Fe) speciation in seawater is dominated by complexation with strong organic ligands throughout the water column and have provided important thermodynamic information about these compounds. Independent work has shown that iron exists in both soluble and colloidal fractions in the Atlantic Ocean. Here we have combined these approaches in samples collected from a variety of regimes within the Atlantic Ocean. We measured the partitioning of Fe between soluble (< 0.02 μm) and colloidal (0.02 to 0.4 μm) size classes and characterized the concentrations and conditional stability constants of Fe ligands within these size classes. Results suggest that equilibrium partitioning of Fe between soluble and colloidal ligands is partially responsible for the distribution of Fe between soluble and colloidal size classes. However, a significant fraction of the colloidal Fe was inert to ligand exchange as soluble Fe concentrations were generally lower than values predicted by a simple equilibrium partitioning model.In surface waters, strong ligands with conditional stability constants of 10¹³ relative to total inorganic Fe appeared to dominate speciation in both the soluble and colloidal fractions. In deep waters these ligands were absent, and instead we found ligands with stability constants 12–15 fold smaller that were predominantly in the soluble pool. Nevertheless, significant levels of colloidal Fe were found in these samples, which we inferred must be inert to coordination exchange.  相似文献   

Distribution of dissolved species and suspended particulate copper in an intertidal ecosystem affected by copper mine tailings in Northern Chile   总被引：1，自引：0，他引：1  

Santiago Andrade  James Moffett  Juan A. Correa   《Marine Chemistry》2006,101(3-4):203-212

The coastline near Chañaral in Northern Chile is one of the most highly Cu-contaminated zones in the world due to discharges from mining activities for more than 60 years. The speciation of Cu has been studied to determine the importance of organic complexation in highly contaminated areas, and to assess the likely physiological impacts of Cu on marine organisms. Dissolved Cu concentrations of up to 500 nM were measured, completely saturating organic ligands and leading to free Cu²⁺ concentrations in excess of 10^− 8 M. These values are higher than those reported in any other marine environment, and because they occur over an extensive area, provide a unique opportunity to study the effects of Cu on marine ecosystems and to see how Cu behaves when its speciation is predominantly inorganic. We found strong gradients in free Cu²⁺ between Chañaral and adjacent areas with lower Cu, where speciation is dominated by organic complexation. There is also a significant increase in the partitioning of Cu onto suspended particles in the contaminated areas, consistent with previous studies that showed that organic ligands stabilize Cu in the dissolved phase, whilst “excess” Cu is rapidly scavenged. Those high dissolved Cu concentrations persist in spite of solid phase partitioning and advective processes along this open-ocean coastline, suggesting that Cu inputs into the system are still very large. Measurements were made using anodic stripping voltammetry with a thin mercury film coated with Nafion, which previous workers have shown can mitigate ambiguity in the data arising from inadvertent reduction of organic complexes. Our findings suggest that this is a useful methodology for contaminated systems.  相似文献   

Thermal balance of the mid-latitude F2-region at night     

G.J. Bailey  R.I. Footitt  R.I. Moffett 《Planetary and Space Science》1979,27(8):1063-1073

The thermal balance of the plasma in the night-time mid-latitude F2-region is examined using solutions of the steady-state O⁺ and electron heat balance equations. The required concentrations and field-aligned velocities are obtained from a simultaneous solution of the time-dependent O⁺ continuity and momentum equations.The results demonstrate the systematic trend for the O⁺ temperature to be 10–20 K greater than the electron temperature during the night at around 300 km, as observed at St. Santin by Bauer and Mazaudier. It is shown that frictional heating between the O⁺ and neutral gases is the cause of the O⁺ temperature being greater than the electron temperature; the greater the importance of frictional heating in the thermal balance the greater is the difference in the O⁺ and electron temperatures. A study is made of the roles played in the thermal balance of the plasma by the thermal conductivity of the O⁺ and electron gases; collisional heat transfer between O⁺ electrons and neutrals; frictional heating between the O⁺ and neutral gases; and advection and convection due to field-aligned O⁺ and electron motions. The results of the study show that, at around 300 km, electron cooling by excitation of the fine structure of the ground state of atomic oxygen plays a major role in the thermal balance of the electrons and, since the temperature of the ions is little affected by this electron cooling process, in determining the difference between the ion and electron temperatures.  相似文献   

Relative flow of H⁺ and O⁺ ions in the topside ionosphere at mid-latitudes     

G.I. Bailey  R.J. Moffett  J.A. Murphy 《Planetary and Space Science》1977,25(10):967-972

Theoretical results on the daily variation of O⁺ and H⁺ field-aligned velocities in the topside ionosphere are presented. The results are for an L = 3 magnetic field tube under sunspot minimum conditions at equinox. They come from calculations of time-dependent O⁺ and H⁺ continuity and momentum balance in a magnetic field tube which extends from the lower F2 region to the equatorial plane (Murphy et al., 1976).There are occasions when ion counterstreaming occurs, with the O⁺ velocity upward and H⁺ velocity downward. The conditions causing this counterstreaming are described: the H⁺ layer is descending whilst O⁺ is supplied from below either to increase the O⁺ concentration at fixed heights or to replace O⁺ ions lost by charge exchange with neutral H. It is suggested that the results of observations at Arecibo by Vickrey et al. (1976) of O⁺ and H⁺ concentrations and counterstreaming velocities are significantly affected by $\text{E}\text{×}\text{B}$ drift.  相似文献   

Interhemispheric flow of thermal plasma in a closed magnetic flux tube at mid-latitudes under sunspot minimum conditions     

G.J. Bailey  R.J. Moffett  J.A. Murphy 《Planetary and Space Science》1978,26(8):753-765

The coupled H⁺ and O⁺ time-dependent continuity and momentum equations are solved within a region of the L = 3 magnetic flux tube lying between (and including) the F2-layers of conjugate hemispheres. The method of solution is an extended and modified version of the Murphy et al. (1976) method. The model is used to study the coupling between the F2-layers of conjugate hemispheres during magnetically quiet periods.The results of the calculations strongly indicate that the protonosphere acts as a reservoir, with variable H⁺ content, which prevents direct coupling between the F2-layers of conjugate hemispheres. However there is generally a significant interhemispheric flow of plasma. This flow is caused by conditions in the summer and winter topside ionospheres and it maintains continuity in the plasma concentration within the protonosphere. There are times when the direction of flow is from the winter hemisphere to the summer hemisphere. It is suggested that maintenance of the winter F2-layer at night is not assisted directly by the F2-layer of the conjugate summer hemisphere.It is shown that during the first few days of protonosphere replenishment after a magnetic storm there is an upflow of H⁺ in the topside ionosphere at all times in the summer hemisphere. There is also an upflow of H⁺ during the daytime in both hemispheres. A comparison with the results obtained when the interhemispheric H⁺ flux is held permanently at zero shows that both F2-layers are little affected by the interhemispheric H⁺ flux. Nevertheless both F2-layers are affected by the H⁺ tube content of the protonosphere. When the H⁺ flux at 1000 km in one hemisphere is much greater than the H⁺ flux at 1000 km in the conjugate hemisphere, there is a corresponding signature in the interhemispheric H⁺ flux.The results suggest that there is insufficient time between magnetic storms for complete replenishment of the protonosphere to occur.  相似文献   

Vibrational nitrogen concentration in the ionosphere and its dependence on season and solar cycle     

A. E. Ennis  G. J. Bailey  R. J. Moffett 《Annales Geophysicae》1995,13(11):1164-1171

A fully time-dependent mathematical model, SUPIM, of the Earth’s plasmasphere is used in this investigation. The model solves coupled time-dependent equations of continuity, momentum and energy balance for the O⁺, H⁺, He⁺, N⁺₂, O⁺₂, NO⁺ ions and electrons; in the present study, the geomagnetic field is represented by an axial-centred dipole. Calculation of vibrationally excited nitrogen molecules, which has been incorporated into the model, is presented here. The enhanced model is then used to investigate the behaviour of vibrationally excited nitrogen molecules with F10.7 and solar EUV flux, during summer, winter and equinox conditions. The presence of vibrational nitrogen causes a reduction in the electron content. The diurnal peak in electron content increases linearly up to a certain value of F10.7, and above this value increases at a lesser rate, in agreement with previous observations and modelling work. The value of F10.7 at which this change in gradient occurs is reduced by the presence of vibrational nitrogen. Vibrational nitrogen is most effective at F-region altitudes during summer daytime conditions when a reduction in the electron density is seen. A lesser effect is seen at equinox, and in winter the effect is negligible. The summer reduction in electron density due to vibrational nitrogen therefore reinforces the seasonal anomaly.  相似文献   

A summary of sulfur dioxide emission rate measuremnts from Guatemalan volcanoes     

RJ Andres  WI Rose  RE Stoiber  SN Williams  O Matías  R Morales 《Bulletin of Volcanology》1993,55(5):379-388

Measurements of the sulfur dioxide (SO₂) emission rate from three Guatemalan volcanoes provide data which are consistent with theoretical and laboratory studies of eruptive and shallow magma chamber processes. In particular, unerupted magma makes a major contribution to the measured SO₂ emission rates at Santiaguito, a continuously erupting dacitic volcanic dome. Varying shallow magma convection rates can explain the variations in SO₂ emission rates at Santiaguito. At Fuego, a basaltic volcano currently in repose, SO₂ emission rate measurements are consistent with a high level magma body that is crystallizing and releasing volatiles. At Pacaya, a continuously erupting basaltic volcano, recent SO₂ emission rate measurements support laboratory simulation studies of strombolian eruptions; these studies indicate that the majority of gas escapes during eruptions and little gas escapes between eruptions.Average SO₂ emission rates over the last 20 years for Santiaguito, Fuego and Pacaya are 80, 160 and 260 Mg/d, respectively. On a global scale, these three volcanoes account for 1% of the annual global volcanic output of SO₂. Santiaguito and Pacaya, together, emit 6% of the total annual SO₂ emitted by continuously erupting volcanoes.Even though SO₂ measurements at these volcanoes have been made infrequently and by different investigators, the collective data help to establish a useful baseline by which to judge future changes. A more complete record of SO₂ emission rates from these volcanoes could lead to a better understanding of their eruption mechanisms and reduce the impact of their future eruptions on Guatemalan society.  相似文献