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101.
Švestka Zdeněk Fárník František Hick Paul Hudson Hugh S. Uchida Yutaka 《Solar physics》1997,176(2):355-371
We demonstrate several events where an eruptive flare close to the limb gave rise to a transient coronal streamer visible in X-rays in Yohkoh SXT images, and analyze one of these events, on 28–29 October 1992, in detail. A coronal helmet streamer began to appear 2 hours after the flare, high above rising post-flare loops; the streamer became progressively narrower, reaching its minimum width 7–12 hours after the flare, and widened again thereafter, until it eventually disappeared. Several other events behaved in a similar way. We suggest that the minimum width indicates the time when the streamer became fully developed. All the time the temperature in the helmet streamer structure was decreasing, which can explain the subsequent fictitious widening of the X-ray streamer. It is suggested that we may see here two systems of reconnection on widely different altitudes, one giving rise to the post-flare loops while the other creates (or re-forms) the coronal helmet streamer. A similar interpretation was suggested in 1990 by Kopp and Polettofor post-flare giant arches observed on board the SMM; indeed, there are some similarities between these post-flare helmet streamers and giant arches and, with the low spatial resolution of SMM instruments, it is possible that some helmet streamers could have been considered to be a kind of a giant arch. 相似文献
102.
Motohiko Kashima Shiro Imawaki Shin-Ichiro Umatani Hiroshi Uchida Yuji Hashibe Hiroshi Ichikawa Masao Fukasawa 《Journal of Oceanography》2003,59(3):291-301
Theoretically, the geostrophic approximation holds for the low-frequency flow field, but no detailed examination has been
done on how well the estimated geostrophic velocity corresponds with the observed velocity. Intensive surveys were carried
out during 1993–1995 in the Kuroshio and its recirculation regions south of Shikoku, Japan, including repeated hydrographic
surveys and direct current measurements at nominal depths of 700, 1500 and 3000 m. For these depth intervals, vertical differences
of estimated geostrophic velocity are compared with those of observed velocity. For the intermediate layer (between 700 and
1500 m depths), the slope of the regression line is 0.99, correlation coefficient is 0.98, and the root-mean-square of difference
from geostrophic balance is 2.8 cm/s which is close to the estimated error of 2.1 cm/s. For the deep layer (between 1500 and
3000 m depths), the corresponding values are 0.82, 0.93, 1.2 cm/s and 2.0 cm/s, respectively. The results indicate that the
estimated geostrophic velocity compares well with the observed velocity in these regions.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
103.
Yasumasa Ogawa Naotatsu Shikazono Daizo Ishiyama Hinako Sato Toshio Mizuta Takanori Nakano 《Mineralium Deposita》2007,42(3):219-233
The Sr, Ba, and rare earth elements (REEs) concentrations and Sr isotopic composition of anhydrite and gypsum have been determined
for samples from the Matsumine, Shakanai, and Hanaoka Kuroko-type massive sulfide–sulfate deposits of northern Japan to evaluate
the mechanisms of sekko (anhydrite and gypsum) ore formation. The Sr isotopic compositions of the samples fall in the range
of 0.7077–0.7087, intermediate between that for middle Miocene (13–15 Ma) seawater (0.7088) (Peterman et al., Geochim Cosmochim
Acta, 34:105–120, 1970) and that for country rocks (e.g., 0.7030–0.7050) (Shuto, Assn Geol Collab Japan Monograph 18:91–105, 1974). The Kuroko anhydrite samples exhibit two types of chondrite-normalized REE patterns: one with a decrease from light REEs
(LREEs) to heavy REEs (HREEs) (type I), and another with a LREE-depleted pattern (type II).
Based on the Sr content and isotopic ratio (assuming an Sr/Ca (mM/M) of 8.7 for seawater), anhydrite is considered to have
formed by mixing of preheated seawater with a hydrothermal solution of Sr/Ca (mM/M) = ca. 0.59–1.36 under the condition in
which the partition coefficient (Kd) ranges between ca. 0.5 and 0.7. This results in the formation of anhydrite with higher
Sr content with an Sr isotopic value close to that of seawater under seawater-dominant conditions.
Larger crystals of type II anhydrite are partly replaced by smaller ones, indicating that anhydrite dissolution and recrystallization
occurred after or during the formation of sekko ore. Gypsum, which partially replaces anhydrite in the Kuroko deposits, also
exhibits two distinct chondrite-normalized REE patterns. Because LREEs are likely to be more readily mobilized during dissolution
and recrystallization, it is hypothesized that LREEs are leached from type I anhydrite, resulting in the formation of type
II anhydrite with LREE-depleted profiles. 相似文献
104.
By using a thermally stratified wind tunnel, we have successfullysimulated stably stratified boundary layers (SBL), in which the meantemperature increases upward almost linearly. We have investigated the flow structure and the effects of near-linearstable stratification on the transfer of momentum and heat. Thevertical profiles of turbulence quantities exhibit different behaviour in two distinct stability regimes of the SBLflows with weak and strong stability. For weak stability cases, theturbulent transfer of momentum and heat is basically similar to that for neutral turbulent boundary layers, although it is weakenedwith increasing stability. For strong stability cases, on the other hand,the time-mean transfer is almost zero over the whole boundary-layer depth.However, the instantaneous turbulent transfer frequently occurs in bothgradient and counter-gradient directions in the lower part of the boundary layer. This is due to the Kelvin–Helmholtz (K–H) shear instability and therolling up and breaking of K–H waves. Moreover, the internal gravity wavesare observed in the middle and upper parts of all stable boundary layers. 相似文献
105.
Geochemical Process of Gas Hydrate Formation in the Nankai Trough Based on Chloride and Isotopic Anomalies in Interstitial Water 总被引:2,自引:0,他引:2
Abstract: Interstitial water expelled from gas hydrate-bearing and -free sediments in the Nankai Trough are analyzed in terms of Cl-, SO4 2 -, δ18 O and δD. The baselines for the Cl- concentration and δ18 O value are close to seawater values (530 mM and 0%), indicating that the interstitial water is of seawater origin. The δD values decrease with depth, implying isotopic exchange of hydrogen between upwelling biogenic methane depleted in D and interstitial water. The Cl- concentrations in gas hydrate-bearing sediments are anomalously low, while the δ18 O and δD values are both high, suggesting that the water forming these gas hydrates was poor in Cl- and enriched in 18 O and D during gas hydrate formation. Calculation of the gas hydrate saturations using Cl "and δ18 O anomalies gives results of up to 80 % in sand, and shows that the δ18 O baseline is not consistent with the Cl" baseline. The δ18 O baseline increases by +1% in gas hydrate-free clay and silt. This is considered to be caused by clustering of water molecules after gas hydrate dissociation in response to the upward migration of the base of gas hydrate stability, as indicated by the presence of a double bottom-simulating reflector at this site. The water clusters enriched in 18 O are responsible for the increase in the δ18 O baseline with normal Cl". The abrupt shallowing of the base of gas hydrate stability may induce the dissociation of gas hydrates and the accumulation of gases in the new stability zone, representing a geological process that increases gas hydrate saturation. 相似文献
106.
Abstract. The Nankai Trough parallels the Japanese Island, where extensive BSRs have been interpreted from seismic reflection records. High resolution seismic surveys and drilling site-survey wells conducted by the MTI in 1997, 2001 and 2002 have revealed subsurface gas hydrate at a depth of about 290 mbsf (1235 mbsl) in the easternmost part of Nankai Trough. The MITI Nankai Trough wells were drilled in late 1999 and early 2000 to provide physical evidence for the existence of gas hydrate. During field operations, continuous LWD and wire-line well log data were obtained and numerous gas hydrate-bearing cores were recovered. Subsequence sedimentologic and geochemical analyses performed on the cores revealed important geologic controls on the formation and preservation of natural gas hydrate. This knowledge is crucial to predicting the location of other hydrate deposits and their eventual energy resource. Pore-space gas hydrates reside in sandy sediments from 205 to 268 mbsf mostly filling intergranular porosity. Pore waters chloride anomalies, core temperature depression and core observations on visible gas hydrates confirm the presence of pore-space hydrates within moderate to thick sand layers. Gas hydrate-bearing sandy strata typically were 10 cm to a meter thick. Gas hydrate saturations are typically between 60 and 90 % throughout most of the hydrate-dominant sand layers, which are estimated by well log analyses as well as pore water chloride anomalies.
It is necessary for evaluating subfurface fluid dlow behavious to know both porosity and permeability of gas hydrate-bearing sand to evaluate subsurface fluid flow behaviors. Sediment porosities and pore-size distributions were obtained by mercury porosimetry, which indicate that porosities of gas hydrate-bearing sandy strata are approximately 40 %. According to grain size distribution curves, gas hydrate is dominant in fine- to very fine-grained sandy strata. 相似文献
It is necessary for evaluating subfurface fluid dlow behavious to know both porosity and permeability of gas hydrate-bearing sand to evaluate subsurface fluid flow behaviors. Sediment porosities and pore-size distributions were obtained by mercury porosimetry, which indicate that porosities of gas hydrate-bearing sandy strata are approximately 40 %. According to grain size distribution curves, gas hydrate is dominant in fine- to very fine-grained sandy strata. 相似文献
107.
We investigated the characteristics of the alkenones produced by a bloom of Emiliania huxleyi in the eastern Bering Sea in 2000. Alkenones were detected in surface waters between 57°N and 63°N, where phosphate concentrations were low and the ammonium/nitrate ratio was high. The total alkenone content (C37:2, C37:3, and C37:4) ranged from 22.0 to 349 μg g−1 in suspended particles and from 0.109 to 1.42 μg g−1 in surface sediments. This suggests that a large proportion of the particulate alkenones synthesized in the surface water rapidly degraded within the water column and/or at the water-sediment interface of the Bering Shelf. The change in the stable carbon isotopic composition (δ13C) of C37:3 alkenone could not be explained only by variation in [CO2(aq)] in the surface water but also depended on the growth rate of E. huxleyi. The alkenone unsaturation index (UK′37) was converted into an alkenone “temperature” with three equations
[Prahl et al 1988],
[Sikes et al 1997] and [Müller et al 1998]; Sikes et al.’s (1997) equation gave the best correlation with the observed sea surface temperature (SST) in the eastern Bering Sea. However, some temperatures estimated by Sikes et al.’s (1997) equation from the UK′37 varied from the observed SST, possibly because of the rapidly changing rate of alkenone synthesis in the logarithmic growth stage or the low rate of alkenone synthesis when nutrients were limiting. Temperatures estimated from UK′37 in the surface sediments (6.8-8.2°C) matched the observed SST in September (7-8°C) but differed from the annual average SST of 4 to 5°C, suggesting that most of the alkenone in the eastern Bering Sea was synthesized during limited periods, for instance, in September. The relative amounts of C37:4 alkenone as proportions of the total alkenones (referred to as C37:4%) were high, ranging from 18.3 to 41.4%. Low-salinity water (<32 psu) within the study area would have contributed to the high C37:4% because a negative linear relationship between C37:4% and salinity was found in this study. 相似文献
108.
Hydrologic and geochemical influences on the dissolved silica concentration in natural water in a steep headwater catchment 总被引:1,自引:0,他引:1
The dissolved silica concentrations in groundwater, springwater, and streamwater were measured on an unchanneled hillslope in the Tanakami Mountains of central Japan. The effects of preferential flowpaths, including lateral and vertical flow in the soil layer and flow through bedrock fractures, on the variation in the dissolved silica concentrations in runoff and groundwater were examined, as were the effects of the mixing of water from geochemically diverse water sources on the dissolved silica concentrations. The mean dissolved silica concentrations in water sampled from 40 cm below the soil surface and in transiently formed groundwater above the soil-bedrock interface during rainfall events were relatively constant, independent of the variation in the mixing ratio of pre-event water and incoming throughfall. These waters were mostly supplied by the vertical infiltration of water in soil. The mean dissolved silica concentrations were similar, regardless of sampling depth, although the mean residence time of the water increased with depth. These results indicated that the dissolved silica concentrations in soil water and transient groundwater were independent of contact time between the water and minerals. The mean dissolved silica concentration in perennially saturated groundwater above the soil-bedrock interface, which was recharged by water infiltrating through soil, and water emerging from bedrock in an area near the spring was more than twice that of transient groundwater, and the variation was relatively large. The mean dissolved silica concentration increased significantly downslope, from perennial groundwater to spring from soil matrix to stream, and the spring and stream concentrations also showed large variations. The dissolved silica concentration was highest in the spring from a bedrock fracture and was relatively constant. The mixing of water from two geochemically diverse water sources, soil and bedrock, controlled the dissolved silica concentrations of the perennial groundwater, the spring from soil matrix, and the stream. Our results demonstrated that in most areas of this headwater catchment, the preferential flowpaths have only a small effect on the dissolved silica concentrations. In a small area, which was < 2% of the total catchment area near the spring, the dissolved silica concentration was controlled by the mixing of water from geochemically diverse water sources. 相似文献
109.
A magnetodynamic model to deal with the acceleration and collimation of jets as a part of the global process of gravitational
contraction of the magnetized gas to the central gravitator is discussed. We first review its application to the star forming
jet case with several observational supporting evidence. Then, a justification will be given for the extension of this to
the AGN jet case, despite of the difference in orders of magnitudes in the scales as well as in the physical parameters. The
results of actual application of this magnetodynamic mechanism to the AGN case will be presented together with the discussions
for the origin of the radio lobes and hotspots, and we show that this mechanism can explain the enhancement of accretion and
the formation of the jet + lobe system consistently with the genetic consideration of the system.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
110.
A supersaline, metal-rich brine (ca. 40 weight% total chloride salt) was extracted from 3708 m depth of well WD-1a in the
Kakkonda Granite by reverse circulation after a standing time about 196 hours. The estimated borehole temperature exceeds
500 °C near the bottom. Tritium content and the relationship between δD and δ18O show that the injected borehole fluid (river water) evidently mixed with an isotopically heavy and ancient fluid. The phase
analysis showed that a gas phase separated from a brine and that a brine concentrated in the borehole as the borehole temperature
recovered after cooling by drilling fluids. We think the original fluid was trapped in the Kakkonda Granite and mixed with
the borehole fluid through fine fractures induced by thermal stress.
Received: 15 May 1997 / Accepted: 24 September 1997 相似文献