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1.
REE diffusion in calcite   总被引：6，自引：0，他引：6  
Chemical diffusion of four rare-earth elements (La, Nd, Dy and Yb) has been measured in natural calcite under anhydrous conditions, using rare-earth carbonate powders as the source of diffusants. Experiments were run in sealed silica capsules along with finely ground calcite to ensure stability of the single-crystal samples during diffusion anneals. Rutherford backscattering spectroscopy (RBS) was used to measure diffusion profiles. The following Arrhenius relations were obtained over the temperature range 600–850°C: DLa =2.6×10−14 exp(−147±14 kJ mol−1/RT) m2 s−1, DNd =2.4×10−14 exp(−150±13 kJ mol−1/RT) m2 s−1, DDy =2.9×10−14 exp(−145±25 kJ mol−1/RT) m2 s−1, DYb =3.9×10−12 exp(−186±23 kJ mol−1/RT) m2 s−1. In contrast to previous findings for refractory silicates (e.g. zircon), differences in transport rates among the REE are not pronounced over the range of temperature conditions investigated in this study. Diffusion of the REE is significantly slower than diffusion of the divalent cations Sr and Pb and slower than transport of Ca and C at temperatures above 650°C. Fine-scale zoning and isotopic and REE chemical signatures may be retained in calcites under many conditions if diffusion is the dominant process affecting alteration.  相似文献   

2.
Paleocene volcanic rocks in West Greenland and Baffin Island were among the first products of the Iceland mantle plume, forming part of a larger igneous province that is now submerged beneath the northern Labrador Sea. A 40Ar/39Ar dating study shows that volcanism commenced in West Greenland between 60.9 and 61.3 Ma and that 80% of the Paleocene lava pile was erupted in 1 million years or less (weighted mean age of 60.5±0.4 Ma). Minimum estimates of magma production rates (1.3×10−4 km3 year−1 km−1) are similar to the present Iceland rift, except for the uppermost part of the Paleocene volcanic succession where the rate decreases to <0.7×10−4 km3 year−1 km−1 (rift). The timing of onset of volcanism in West Greenland coincides with the opening of the northern Labrador Sea and is also strikingly similar to the age of the oldest Tertiary volcanic rocks from offshore SE Greenland and the British–Irish province. This is interpreted as manifesting the impact and rapid (>1 m/year) lateral spreading of the Iceland plume head at the base of the Greenland lithosphere at 62 Ma. We suggest that the arrival, or at least a major increase in the flux, of the Iceland mantle plume beneath Greenland was a contributing factor in the initiation of seafloor spreading in the northern Labrador Sea. Our study has also revealed a previously unrecognised Early Eocene volcanic episode in West Greenland. This magmatism may be related to movement on the transform Ungava Fault System which transferred drifting from the Labrador Sea to Baffin Bay. A regional change in plate kinematics at 55 Ma, associated with the opening of the North Atlantic, would have caused net extension along parts of this fault. This would have resulted in decompression and partial melting of the underlying asthenosphere. The source of the melts for the Eocene magmatism may have been remnants of still anomalously hot Iceland plume mantle which were left stranded beneath the West Greenland lithosphere in the Early Paleocene.  相似文献   

3.
The increased depth and volume of melting induced in a higher temperature Archaean mantle controls the stability of the lithosphere, heat loss rates and the thickness of the oceanic crust. The relationship between density distributions in oceanic lithosphere and the depth of melting at spreading centres is investigated by calculating the mineral proportions and densities of residual mantle depleted by extraction of melt fractions. The density changes related to compositional gradients are comparable to those produced by thermal effects for lithosphere formed from a mantle which is 200°C or more hotter than modern upper mantle. If Archaean continental crust formed initially above oceanic lithosphere, the compositional density gradients may be sufficient to preserve a thick Archaean continental lithosphere within which the Archaean age diamonds are preserved. The amount of heat advected by melts at mid-ocean ridges today is small but heat advected by melting becomes proportionally more important as higher mantle temperatures lead to a greater volume of melt and as the rate of production of oceanic plates increases. Archaean tectonics could have been dominated by spreading rates 2–3 times greater than now and with mantle temperatures between ca. 1600°C and 1800°C at the depth of the solidus. Mid-ocean ridge melting would produce a relatively thick but light refractory lithosphere on which continents could form, protected from copious volcanism and high mantle temperatures.  相似文献   

4.
We have developed techniques to determine238U,234U and232Th concentrations in seawater by isotope dilution mass spectrometry. U measurements are made using a233U236U double spike to correct for instrumental fractionation. Measurements on uranium standards demonstrate that234U/238U ratios can be measured accurately and reproducibly.234U/238U can be measured routinely to ± 5‰ (2σ) for a sample of 5 × 109 atoms of234U (3 × 10−8 g of total U, 10 ml of seawater). Data acquisition time is 1 hour. The small sample size, high precision and short data acquisition time are superior to-counting techniques.238U is measured to ± 2‰ (2σ) for a sample of 8 × 1012 atoms of238U ( 3 × 10−9 g of U, 1 ml of seawater).232Th is measured to ± 20‰ with 3 × 1011232Th atoms (10−10 g232Th, 1 1 of seawater). This small sample size will greatly facilitate investigation of the232Th concentration in the oceans. Using these techniques, we have measured238U,234U and232Th in vertical profiles of unfiltered, acidified seawater from the Atlantic and238U and234U in vertical profiles from the Pacific. Determinations of234U/238U at depths ranging from 0 to 4900 m in the Atlantic (7°44′N, 40°43′W) and the Pacific (14°41′N, 160°01′W) Oceans are the same within experimental error (± 5‰,2σ). The average of these234U/238U measurements is 144 ± 2‰ (2σ) higher than the equilibrium ratio of 5.472 × 10−5. U concentrations, normalized to 35‰ salinity, range from 3.162 to 3.281 ng/g, a range of 3.8%. The average concentration of the Pacific samples (31°4′N, 159°1′W) is 1% higher than that of the Atlantic (7°44′N, 40°43′W and 31°49′N, 64°6′W).232Th concentrations from an Atlantic profile range from 0.092 to 0.145 pg/g. The observed constancy of the234U/238U ratio is consistent with the predicted range of234U/238U using a simple two-☐ model and the residence time of deep water in the ocean determined from14C. The variation in salinity-normalized U concentrations suggests that U may be much more reactive in the marine environment than previously thought.  相似文献   

5.
Analytical procedures in the determination of iodine-129 (half-life: 1.6×107 y) have been studied using accelerator mass spectrometry (AMS), with special references to the separation procedures of iodine from soil samples for the AMS measurement. Iodine was successfully volatilized from soil samples by pyrohydrolysis at 1000 °C and collected in a trap solution. Iodine was purified from the matrix by solvent extraction. Finally, it was precipitated as silver iodide to make a target for AMS. In order to obtain information on the 129I/127I ratio in a chemical blank (or iodine carrier), we have determined the ratios in several iodine reagents and found that the ratios fell in a narrow range around 1.7×10−13. The detection limit for soil sample (1 g material) by the present method was about 0.01 mBq/kg or 4×10−11 as the ratio of stable iodine (129I/127I ratio), i.e. these values were much better than that by neutron activation analysis (NAA) used in our previous studies. We have applied this method in the analysis of soil samples collected from different places in Japan. We could successfully determine 129I in soil samples with low 129I concentrations, which could not be detected by NAA. Sample size necessary for the soil analysis by AMS was only about 0.5 g or less, whereas about 100 g of the sample were required for NAA [Muramatsu, Y., Ohmomo, Y., 1986. Iodine-129 and iodine-127 in environmental samples collected from Tokaimura/ Ibaraki, Japan. Sci. Total Environ. 48, 33-43]. Using this method, new data were obtained for the 129I levels in 20 soil samples collected from background areas far from nuclear facilities, and the ranges were 1.4×10−5−4.5×10−3 Bq/kg as 129I concentrations and 3.9×10−11−2.2×10−8 as 129I/127I ratios. These values are useful in understanding the 129I levels in Japanese environments. Higher 129I concentrations were observed in forest soils than those in field and rice paddy soils should be related to the interception effect of atmospheric 129I due to tree canopies. Relatively high 129I/127I ratios found in rice paddy soils could be explained by their low stable iodine concentrations which were caused by the desorption of stable iodine from the rice paddies during the cultivation.  相似文献   

6.
Noble gases were extracted in steps from grain size fractions of microdiamonds ( < 100 μm) from the Kokchetav Massif, Northern Kazakhstan, by pyrolysis and combustion. The concentration of 4He in the diamonds proper (liberated by combustion) shows a 1/r dependence on grain size. For grain diameters > 15 μm the concentration also decreases with the combustion step. Both results are clear evidence that 4He has been implanted into the diamonds from -decaying elements in the surrounding matrix. The saturation concentration of 4He(5.6 × 10−4 cm3 STP/g) is among the very highest observed in any terrestrial diamonds. Fission xenon from the spontaneous fission of 238U accompanies the radiogenic 4He; the 136Xef/4He ratio of (2.5 ± 0.3) × 10−9 agrees well with the production ratio of 2.3 × 10−9 expected in a reservoir where Th/U 3.3. Radiogenic 40Ar is predominantly ( > 90%) set free upon combustion; it also resides in the diamonds and appears to have been incorporated into the diamonds upon their formation.

3He, on the other hand is mainly released during pyrolysis and hence is apparently carried by ‘contaminants’. The concentration in the diamonds proper is of the order of 4 × 10−12 cm3 STP/g, with a 3He/4He ratio of 1 × 10−8. Excess 21Ne, similarly, appears to be present in contaminants as well as in diamonds proper. These two nuclides in the contaminants must have a nucleogenic origin, but it is difficult to explain their high concentrations.  相似文献   


7.
Noble gas elemental and isotopic abundances have been analysed in eight samples of youthful basaltic glass dredged from three different locations within the Lau Backarc Basin: (1) the King's Triple Junction, (2) the Central Lau Spreading Centre at 18°S and (3) the Eastern Lau Spreading Centre at 19°S. Samples from the Lau central and eastern spreading centres have MORB-like helium isotopic ratios of approximately 1.2 × 10−5 (8.5 R/RA). In contrast, the samples from the King's Triple Junction yield helium isotopic ratios averaging 9.4 (±0.8) × 10−6 (6.7 ± 0.6 R/RA), systematically lower than the MORB-like value, which may be reflecting the addition of radiogenic 4He released from the descending slab. Neon isotopic ratios are enriched in 20Ne and 21Ne with respect to atmospheric ratios by as much as 23% and 62% respectively. These observations further confirm that non-atmospheric neon is a common characteristic of samples derived from the mantle. The helium and neon isotopic signatures in the samples can be explained by mixing of a primordial solar component, radiogenic and nucleogenic components produced by radioactive processes inside the Earth, and an atmospheric component. This reconnaissance survey of noble gases in a backarc basin indicates that current volcanism is dominated by magmas from the mantle wedge, a source similar to that from which MORBs are derived. The heavier noble gases (argon, krypton and xenon), however, show more atmosphere-like compositions, either indicating strong interaction of the magmas with the atmosphere or the presence of a recycled component derived from the underlying subducting slab.  相似文献   

8.
He diffusion in olivine   总被引：1，自引：0，他引：1  
Helium diffusion in olivine (dunite xenolith) has been measured in the temperature range 1180–1460°C; a linear Arrhenius function was obtained with an activation energy of 120−27+32 kcal/mole, and a pre-exponential factor (D0) = 2.2 × 108 cm2/s.

Diffusion mechanisms are not a viable means of degassing He from the mantle. Olivine phenocrysts can be expected to retain previously trapped He, during cooling in extrusive basalts, provided the flow units are thinner than 50 m; xenoliths will retain mantle He signatures only if magma transport times are less than 50 years, or if the He fugacity in the magma is high enough to prevent xenolith degassing. The lower oceanic crust is probably substantially degassed of He. Trapped He will be qualitatively retained in quenched submarine basalt glass only if the cooling rate is faster than 5 × 1014°C/m.y.; glass at several centimeters depth in a basalt flow (near the spherulite zone) will have cooling rates lower than this, so He loss may be significant in many basalt glass samples.  相似文献   


9.
Argon, krypton, chlorine, bromine, and iodine were measured in a homogeneous population of high-salinity hydrothermal fluid inclusions from the Tertiary-age Mississippi Valley-type (MVT) lead-fluorite-barite deposits at Hansonburg, New Mexico to establish new types of evidence for the history of both the fluid and the major dissolved salts. Noble gases and halogens in fluid inclusions containing 10−10–10−9 L of brine (Cl= 3 molal) were analyzed by laser microprobe noble-gas mass spectrometry (lmngms) on neutron-irradiated samples.

The concentrations of36Ar (4.7 × 10−8 molal) and84Kr1.8 × 10−9 molal) in the fluid inclusions are equal to those of fresh surface waters in equilibrium with air at approximately20 ± 5°. The mole ratios ofBr/Cl (1.2 × 10−4) andI/Cl (1–2 × 10−6) are among the lowest measured in any natural waters, similar to those of modern brines formed by dissolution of Permian NaCl-bearing evaporites in southeast New Mexico.40Ar/36Ar ratios (600) are twice that of air, and indicate that the fluid inclusions had excess radiogenic40Ar (1.4 × 10−5 molal) when trapped. The amount of excess40Ar appears to be too large to have been acquired with Cl by congruent dissolution of halite-bearing evaporites, and possibly too small to have been acquired with Pb by congruent dissolution of granitic basement rocks with Proterozoic KAr ages.

From thelmngms data, combined with published Pb and S isotope data, we infer the following sequence of events in the history of the Hansonburg MVT hydrothermal brine: (1) the brine originated as relatively dilute meteoric water, and it did not gain or lose atmospheric Ar or Kr after recharge; (2) the originally dilute fluid acquired the bulk of its Cl and sulfate in the subsurface after recharge by dissolving halite-bearing Permian? marine evaporites; (3) the high salinity brine then acquired most of its Pb and excess radiogenic40Ar from interactions with aquifer rocks other than evaporites, possibly clastic sedimentary rocks or basement rocks with Phanerozoic KAr “ages”; and (4) the brine deposited fluorite without having boiled or degassed.  相似文献   


10.
The impact of domestic sewage effluent (SE) on the dynamics of phytoplankton assemblages from Bedford Basin was evaluated in the laboratory. Phytoplankton production and chlorophyll a increased proportionally with SE enrichment. Phytoplankton species composition also changed. The potentially harmful diatoms, Pseudonitzschia spp., present initially in small numbers (600 cells 1−1) in Bedford Basin seawater, and became dominant (3–5×106 cells 1−1) when the seawater was enriched with 0.5–5% untreated SE. With higher proportions of SE, other harmful species such as Fragilaria spp. and Euglena spp. became dominant (7−15×106 and 2.2×104 cells 1−1, respectively). Treatment of SE with UV light or activated charcoal seems to favour growth of benign species, such as Chaetoceros socialis, Skeletonema costatum and Thalassiosira spp., but not harmful species such as Pseudonitzschia spp. Further research on UV treatment of domestic sewage is recommended.  相似文献   

11.
238U, 232Th, 230Th and 226Ra abundances have been measured in six samples of recent Hawaiian basalt by high precision mass spectrometry, in an attempt to compare the melting process in plumes and at spreading ridges. The data reveal a very small range in (230Th/238U) activity ratio up to a maximum value of 1.02 ± 0.01, and (226Ra/230Th) activity ratios which lie between 1.10 ± 0.015 and 1.19 ± 0.02. UTh and RaTh abundances are linearly correlated demonstrating that the disequilibria predate crystallisation and differentiation. Using recently published estimates for the bulk partition coefficients of U and Th, the results are consistent with melting rates > 10−3 kg m−3 a−1 at porosities < 10−3 for dynamic fractional melting in the garnet stability field.  相似文献   

12.
In 1989, in a hydrological research programme within a deacidification project in the Gårdsjön area in southwest Sweden, flow paths and residence times of soil water and groundwater in microcatchments were examined to support the interpretation of the hydrochemical changes. Saturated hydraulic conductivity and soil water retention were analysed on more than 100 cylinder samples. The catchments have shallow sandy-silty till soil with a mean depth in the main catchment of 43 cm. Porosity of the mineral soil in the main catchment was high and ranged from 38 to 85%. The samples from the B-horizon had generally higher porosity. Porosity and the content of organic matter were correlated. The soil water retention was relatively high at all tensions, likely owing to the high content of organic matter. Dissolved organic substances were most probably transported from the shallow soil on the steep sides of the catchment down to the valley where it precipitated. The high porosities could be a consequence of long-term weathering, provided that the organic substances present have increased the leaching of the weathering products. Measured values of saturated hydraulic conductivity were close to log-normally distributed with a mean for all samples of 3 × 10−5 m s−1. There was a significant increase in conductivity toward the ground surface with the mean conductivity of the samples in the uppermost 10 cm of the mineral soil of 4 × 10−5 m s−1, which was about 13 times higher than the conductivity of 3 × 10−6 m s−1 at 1 m depth. From the relationship between runoff at the catchment outlet and groundwater levels, the conductivity was estimated to be 15–200 times higher in the upper soil layer than in the deeper ones. In one profile, 44–64% of the yearly lateral flow was estimated to occur above 30 cm depth. The conductivity was correlated with the content of drainable water, which indicated the importance of the largest pores for the saturated hydraulic conductivity.  相似文献   

13.
We have analyzed helium ages of apatites from several boreholes in the Otway basin, Australia, to evaluate whether laboratory helium diffusivity can be accurately extrapolated to conditions relevant in nature. Downhole apatite helium ages define a broad swath of values from 78–71 Ma at the surface (15°C) to nearly zero at depths corresponding to ambient temperatures of 80°C. The width of the swath results from uncertainties in corrected borehole temperatures, differences in the thermal history experienced by the various boreholes, and possibly from slightly different helium diffusivities among the detrital apatite grains studied. In the eastern Otway basin, the shape and position of the helium age profile is in good agreement with predictions based on the extrapolation of laboratory diffusivity data for Durango apatite coupled with published thermal histories for this part of the basin. In contrast, helium ages are much younger than predicted in the western Otway basin. Based on measured ages from Otway sediments, which have been essentially isothermal over the last few million years, an empirical diffusivity (D/a2) of 2×10−15 s−1 can be assigned to apatites residing at downhole temperatures of 67–97°C. This empirical diffusivity is consistent with laboratory diffusion measurements, demonstrating that such measurements are reasonably accurate and can be applied with confidence to natural geologic settings. Given this confirmation of the laboratory diffusivity data, the discrepancy between the observed and modeled helium age profiles in the western Otway basin suggests that these sediments recently experienced higher temperatures than presently supposed.  相似文献   

14.
In 1996, long-term sealed-hole hydrological observatories with subseafloor temperature and pressure sensors were installed in four cased holes drilled by the Ocean Drilling Program into sedimented young oceanic crust east of the Juan de Fuca Ridge. Data recovered over a year later showed that all four holes displayed temperature profiles indicative of vertical fluid flow immediately prior to their being sealed. Warm water was being produced from basement in two cases, and cool ocean bottom water was being drawn into basement at the others. Linear flow rates of 60–200 m/h were estimated from the perturbation of the temperature profiles relative to undisturbed geothermal gradients at the sites. The pressure differentials driving the flow were also measured at the time of the observatory installations, allowing estimates of permeabilities of the upper crustal sections penetrated by the holes. Estimated permeabilities vary systematically with age, ranging from about 10−10 m2 in the youngest site (0.9 Ma) to 10−12 m2 in the oldest site (3.6 Ma), confirming an apparent reduction of permeability with age determined with packer experiments at three of the same sites. Combined with other estimates of permeabilities in the same holes using methods with different scales of investigation, the new permeability estimates also provide evidence for a significant scale dependence of permeability in the upper oceanic crust.  相似文献   

15.
Rb-Sr mineral data are presented for the Sudbury and Mackenzie dolerites of Canada and for dolerites and lamprophyres from southwest Greenland. Five mineral isochrons or errorchrons, based chiefly upon feldspar separates, agree with twelve biotites from dolerites in defining best-fit ages between 1260 and 1190 m.y. Much older K-Ar and Rb-Sr mineral ages from country rocks demonstrate that the dolerite results are not due to regional heating, and basaltic magmatism in both regions between 1260 and 1190 m.y. is indicated (λ(87Rb) = 1.42 × 10−11 yr−1).

This activity can be correlated with extensive dolerite sills in Sweden and Finland, the subject of parallel studies, which yield six mineral isochrons or errorchrons, ten Rb-Sr biotite ages from dolerites, and determinations by other methods falling between 1290 and 1155 m.y., although the Rb-Sr biotite ages are all grouped in the 1250-1210 m.y. range.

Palaeomagnetic poles from the dolerites define tight clusters for each of Canada/Greenland and Fennoscandia. Superimposition of the two groups of poles leads to a non-unique reconstruction in which Fennoscandia may have adjoined Canada/Greenland at 1260-1190 m.y., but in an orientation quite different from that established for 1000-850 m.y. The necessary net rotation of Fennoscandia through 90° may have been achieved by splitting, separation and final reunion of the continents into a different relative disposition between 1190 and 1000 m.y. This favours the involvement of plate tectonic processes in the Grenville-Sveconorwegian orogeny. The 1260-1190 m.y. dolerites may represent the beginning of a continental separation which preceded the Grenville orogeny, although other causes for the magmatism cannot be ruled out.  相似文献   


16.
A soil-water flux sensor was developed, which determines the flux value from the difference between downstream and upstream temperatures at some distances from an artificial heat source. It can detect flux values ranging from several mm hr.−1 to as small as 0.01 mm hr.−1. Design and calibration of the sensor are described.

The sensor was applied to the field studies of transfer processes in a surface soil, including rainwater infiltration, upward soil-water flow during evapotranspiration, and their effects on the water table level. Cl− accumulation in the surface soil is discussed on the basis of upward water flux and Cl− content observed.  相似文献   


17.
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18.
Bacterial abundances and activity, estimated by 4′,6-diamidino-2-phenylindole staining (DAPI) and the reduction of 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyl tetrazolium chloride (INT), were investigated in two oligotrophic artificial groundwater lakes and the surrounding aquifers. To evaluate the effect of lake water on groundwater downstream, samples were taken from wells at different distances from the lakes, and the total number of bacteria and the number of active bacteria in these samples were compared with samples collected upstream. In addition, sterilized sandy sediments were exposed in groundwater wells to measure the number and activity of bacteria attached to particles. At one of the study sites, where the lake sediments were disturbed by dredging, total bacterial abundance and the number of respiring bacteria in the groundwater aquifer was clearly influenced by the lake water. The average bacterial abundances decreased from 2.6 ± 1.9 × 105 cells ml−1 in the well closest to the lake (S2) to 2.9 ± 3.8 × 104 cells ml−1 in the most distant one (S4), which was equivalent to cell numbers in the upstream well. The number of respiring bacteria showed a similar tendency with 1.3 ± 2.7 × 104 active cells ml−1 in S2 and 1.9 ± 1.5 × 103 active cells ml−1 in S4. At the second study site, which was not influenced by dredging, bacteria in the downstream wells seemed not to be affected by the lake water. The number and activity of bacteria, which colonized exposed sediments, were not significantly different in the upstream and downstream wells, indicating a minor influence of lake water on this habitat. Our results suggest that gravel-pit lakes may influence the free living bacterial assemblages in nearshore groundwater systems, but do not visibly affect numbers and activity of bacteria attached to the surface of aquifer sediments.  相似文献   

19.
We report the first measurements of hydrodynamic dispersion in a microfractured granite using a combination of novel techniques. A fracture network was induced in a cylindrical plug of Ailsa Craig micro-granite by thermal stressing, to produce an isotropic network of fractures with an average aperture of  0.3 μm, a density of approximately 4 × 104 fractures/mm3 and a permeability of 5.5 × 10− 17 m2. After saturating the cores with 0.01 M NaCl solution a step in the concentration profile to 1 M was advected into the plug at flow rates of 0.07 to 2.13 cm3 h− 1. The longitudinal electrical impedance of the plug was measured continuously as the solute front advected through its length until the plug was saturated with the concentrated electrolyte. Analysis of the impedance versus time relationships allows the derivation of the longitudinal dispersion coefficient, DL, and hydrodynamic retardation, RH. The Peclet number–dispersion relationship for the micro-fracture network is very similar to that predicted for other, radically different, fracture networks. Thus dispersion may be more dependent on fracture connectivity and length than fracture density and display a relationship similar to that shown by particle beds and clastic sandstones. The high retardation values observed (2.2–4.9) reflect flow behaviour within a fracture network with a proportion of ‘blind’ sections, and demonstrates how such networks can slow the advance of conservative solute components.  相似文献   

20.
North-seeking bacteria (NSB) with 1 μm diameters migrate to the S pole only. They were applied to identify the S pole determination on a polished surface of magnetite-rich pyroxenite whose natural remanent magnetization (NRM) intensity was 5.64 × 10−3 Am2 kg−1. The microscopic observations were performed under dark-field illumination in a controlled magnetic field to 10 μT. The NSB formed clusters on limited areas of magnetite grains and scattered over the whole magnetite grains.

The NRM decreased to 1.02 × 10−5 Am2 kg−1 by alternating field (AF) demagnetization to 60 mT but no clusters appeared, while small populations of the NSB scattered on each grain. These scattered bacteria may gather toward the S pole resulting from magnetic domain walls.

When the sample acquired saturation isothermal remanent magnetization (SIRM) to 1 T, the NSB formed dense clusters at the opposite side to the applied field direction on the many grains as expected. This evidence indicated that the NSB can be useful micro-organisms for the determination of fine magnetic structures. Some grains also had NSB clusters at the edge of the grains toward the field direction or did not exhibit any clusters. The complicated distribution of the clusters (the S poles) may be explained by shape anisotropy of the magnetic grains.  相似文献   


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