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1.
The oxygen isotope records of both benthic and planktonic Foraminifera in five piston cores, collected from the region between the Oyashio and Kuroshio Currents near Japan, clearly show the marked latitudinal shifts of these two currents during the past 25 kyr. Under the present hydrographic condition, a clear relationship between the sea‐surface temperature (SST) and oxygen isotope differences from benthic to planktonic Foraminifera is observed in this region. Using this relationship, we find decreased SSTs of 12–13°C (maximum 15°C) in the southernmost core site at the Last Glacial Maximum (LGM), indicating the Oyashio Current shifted southward. The SSTs at the southern two core sites abruptly increased more than 10°C at 10–11 ka, suggesting the Kuroshio Current shifted northward over these sites at 10–11 ka. In contrast, the northern two core sites have remained under the influence of the cold Oyashio Current for the past 25 kyr. With the reasonable estimate of bottom‐water temperature decrease of 2.5°C at the LGM, the SSTs estimated by this new method give exactly the same SST values calculated from Mg/Ca ratio of planktonic Foraminifera, allowing palaeosea‐surface salinities to be reconstructed. The result suggests that the ice volume effect was 1.0 ± 0.1‰ at the LGM. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   
2.
Phase Relations on the Actinolite-Pargasite Join   总被引:1,自引:0,他引:1  
Phase relations along the join Ca2Mg4Fe2+Si8O22 (OH)2 (Actinolite)-NaCa2Mg3?2Fe0?82+AlSi6Al2O22(OH)2 (Pargasite) have been studied at PH2O = 1 kb andthe oxygen fugacities defined by the iron-wustite(IW) buffer. Actinolite and bornblende are separated by a solvus and thefield of actinolite+hornblende+vapor is present in the regionbetween Ac85Pa15 and Ac55 Pa45 at 680 ?C. Complete miscibilityis achieved at 720 ?C. At temperatures higher than the solvusthere is a continuous solid solution series between the twoend members. The stability field of amphibole solid solutiongradually increases with increasing pargasite content in actinolite.The phase assemblages at temperatures higher than those of asolid solution series between the two end members change withincreasing pargasite content in the bulk composition as follows;Act+Cpx+Qz+V, ActHbl+Cpx+Opx+Qz+V, Hbl+Cpx+Opx+Pl+V and Hbl+Cpx+Pl+Ol+V. In comparison with the Fe-free system, the extent of the miscibilitygap between actinolite and hornblende is reduced by an increasein the Fe2+ content. The present study should provide an adequatebasis for the interpretation of actinolite-hornblende pairsin metamorphic rocks.  相似文献   
3.
Isoprenoid glycerol dialkyl glycerol tetraethers (GDGTs) and alkenones were analyzed in sediment samples retrieved from Ocean Drilling Program Site 1241 covering the last 150000 years to understand the hydrological evolution of the eastern Pacific warm pool (EPWP). GDGT and alkenone concentrations showed higher values in marine isotope stage (MIS)-2 and MIS-6, which suggests the enhancement of primary production at glacial maxima. $ {\text{TEX}}_{86}^{\text{H}} $ - and $ U_{ 3 7^\prime }^{\text{K}} $ -derived temperature depicted different temperature evolutions. $ U_{ 3 7^\prime }^{\text{K}} $ -derived temperature was marked by small variation during the glacial–interglacial cycles, whereas $ {\text{TEX}}_{86}^{\text{H}} $ -derived temperature showed pronounced glacial–interglacial variation that was similar to Mg/Ca-derived temperature records from nearby cores in the EPWP. Given that enhanced primary production during glacial maxima suggests nutricline shoaling, unchanged $ U_{ 3 7^\prime }^{\text{K}} $ over glacial–interglacial cycles can be interpreted as the shift of alkenone production depth. $ {\text{TEX}}_{86}^{\text{H}} $ seems not to be influenced by glacial–interglacial changes in nutricline depths, recording an integrated temperature in surface and thermocline water. The shallow nutricline in the EPWP during glacial maxima most likely reflected the intense formation of Antarctic intermediate water.  相似文献   
4.
Northward flowing coastal currents along the western margin of India during winter–spring advect low-salinity Bay of Bengal water in to the Eastern Arabian Sea producing a distinct low-salinity tongue, the strength of which is largely governed by the freshwater flux to the bay during summer monsoons. Utilizing the sedimentary records of δ18OG. sacculifer, we reconstructed the past salinity-gradient within that low-salinity tongue, which serves as a proxy for the variation in freshwater flux to the Bay of Bengal and hence summer monsoon intensity.The north–south contrast in the sea level corrected (residual)-δ18OG. sacculifer can be interpreted as a measure of surface salinity-contrast between those two locations because the modern sea surface temperature and its past variation in the study region is nearly uniform. The core-top residual-δ18OG. sacculifer contrast of 0.45‰ between the two cores is assumed to reflect the modern surface salinity difference of 1 psu and serves as a calibration for past variations.The residual-δ18OG. sacculifer contrast varies between 0.2‰ at 75 ky B.P. (i.e., late-Marine Isotope Stage 5) and 0.7‰ at 20 ky B.P. (i.e., Last Glacial Maximum), suggesting that the overall salinity difference between the northern- and southern-end of the low-salinity tongue has varied between 0.6 and 1.6 psu. Considerably reduced difference during the former period than the modern suggests substantially intensified and northward-extended low-salinity tongue due to intense summer monsoons than today. On the other hand, larger difference (1.6 psu) during the latter period indicates that the low-salinity tongue was significantly weakened or withdrawn due to weaker summer monsoons. Thus, the salinity-gradient in the eastern Arabian Sea low-salinity tongue can be used to understand the past variations in the Indian summer monsoons.  相似文献   
5.
The join tremolite (Tr)-pargasite (Pa) was studied at temperatures between 800 and 1150°C under water vapour pressure of 10 kbar. The results show a continuous solid solution of amphibole between the composition Tr80Pa20 and Pa100 at 800°C and 10kb. Pargasite melts incongruently and breaks down at high temperature to clinopyroxene+forsterite+spinel+L+V. A single phase amphibole with composition lying between Tr80Pa20 and nearly pure Pa, breaks down to amphibole of different composition plus other phases. The stability fields of amphibole spread toward higher temperature side with increasing pargasite content, and pargasite itself has the widest stability field. At subliquidus, the composition of amphibole coexisting with other phases becomes more pargasitic with increasing temperature. The compositions of liquid, which are formed by partial melting of amphibole of Tr40Pa60 composition (Fo-normative) under water vapour pressure of 10 kbar, are alumina-rich and Qz-normative.  相似文献   
6.
The ages of fossil planktonic foraminifera,Pulleniatina obliquiloculata, in sediments (core 3bPC) from the western North Pacific were determined by aspartic acid chronology, which uses the racemization reaction rate constant of aspartic acid (kAsp). Aspartic acid racemization-based ages (Asp ages) ranged from 7,600 yrBP at the surface, to 307,000 yrBP at a depth of 352.9 cm in the sediments. This sediment core was also dated by the glacial-interglacial fluctuation of δ18O chronology, and the ages determined by both chronologies were compared. The ages derived from aspartic acid chronology and δ18O stratigraphy were more or less consistent, but there appeared to be some differences in age estimates between these two dating methods at some depths within the core. In the core top sediments, the likely cause for the age discrepancy could be the loss of the surface sediment during sampling of the core. At depths of 66.3 and 139 cm within the core, Asp ages indicated reduced sedimentation rates duringca. 60,000-80,000 yrBP andca. 140,000–190,000 yrBP. The maximum age differences in both chronologies are 33,000 yr and 46,600 yr during each of these periods. These anomalous reductions in sedimentation rates occurring during these periods could possibly be related to some geological events, such as an increased dissolution effect of the calcium carbonate in the western North Pacific. Another possible reason for these age differences could be the unreliability in δ18O ages of core 3bPC as they were estimated by δ18O ages of another core, 3aPC.  相似文献   
7.
A method is proposed by which the degree of attrition of the tests of certain foraminifera species, such as Globorotalia menardii and Globorotalia tumida, is used to “scale” the amount of CaCO3 that has been dissolved from sediment. The scale is calibrated experimentally in the laboratory. The method has been applied to three calcareous cores from the Pacific and the Indian Oceans. It is shown that the original CaCO3 contents in these cores were high (82–95%) and relatively uniform compared to the present down-core values. About 65 to 85% of the originally deposited CaCO3 has been dissolved, corresponding to dissolution rates on the order of 0.1-0.3 moles/cm2/yr. These results indicate that appreciable solution could have occurred on sea floor rich in calcareous sediments and that the variation in CaCO3 content in a core may have resulted largely from dissolution. The difference in the degree of solution between glacial and interglacial sediments in these cores is not so distinct, with ? 10% less intense dissolution during glacial times on the average. However, the dissolution minimum occurring around the late Wisconsin glaciation (10,000–20,000 yr B.P.) previously noted in several cores elsewhere is confirmed. At that time, near the site of core M70 PC-20 in the southwest Pacific, the CO32? concentration of the bottom water is estimated to have been approximately 5% higher than the present value, and the calcite lysocline was about 300 m deeper. To evaluate possible variations in CaCO3 deposition rate across the glacial-interglacial transitions requires precise age control, which the present study lacks.  相似文献   
8.
Abstract— A new insight into carbon and hydrogen isotope variations of insoluble organic matter (IOM) is provided from seven CM chondrites, including Murchison and six Antarctic meteorites (Y‐791198, Y‐793321, A‐881280, A‐881334, A‐881458 and B‐7904) as well as Murchison IOM residues after hydrous pyrolysis at 270–330 °C for 72 h. Isotopic compositions of bulk carbon (δ13Cbulk) and hydrogen (δD) of the seven IOMs vary widely, ranging from ?15.1 to ?7.6%0 and +133 to +986%0, respectively. Intramolecular carboxyl carbon (δ13CCOOH) is more enriched in 13C by 7.5. 11%0 than bulk carbon. After hydrous pyrolysis of Murchison IOM at 330 °C, H/C ratio, δ13Cbulk, δ13CCOOH, and δD values decrease by up to 0.31, 3.5%0, 5.5%0, and 961%0, respectively. The O/C ratio increases from 0.22 to 0.46 at 270 °C and to 0.25 at 300 °C, and decreases to 0.10 at 330 °C. δ13Cbulk‐δD cross plot of Murchison IOM and its pyrolysis residues shows an isotopic sequence. Of the six Antarctic IOMs, A‐881280, A‐881458, Y‐791198 and B‐7904 lie on or near the isotopic sequence depending on the degree of hydrous and/or thermal alteration, while A‐881334 and Y‐793321 consist of another distinct isotope group. A δ13Cbulk‐δ13CCOOH cross‐plot of IOMs, including Murchison pyrolysis residues, has a positive correlation between them, implying that the oxidation process to produce carboxyls is similar among all IOMs. These isotope distributions reflect various degree of alteration on the meteorite parent bodies and/or difference in original isotopic compositions before the parent body processes.  相似文献   
9.
We conducted paired measurements of the Mg/Ca ratio and δ18O of planktonic foraminifera, Globigerina bulloides, from a sediment core (MD01‐2420) off central Japan in the northwest Pacific, to reconstruct current movements since the Last Glacial Maximum (LGM). These methods make it possible to determine the magnitude and timing of the sea surface temperature (SST) changes and to reconstruct the variations of the past seawater δ18O (δ18Ow) off central Japan. The amplitude of Mg/Ca‐based SST changes between the Holocene and the LGM was about 10°C. The strong resemblance of the SSTs estimated from both methods, Mg/Ca‐based and δ18O‐based, suggests that the SST changes were caused primarily by latitudinal displacement of the Kuroshio–Oyashio currents and no distinct change in the carbonate dissolution of the core. The southward migration of the water mass was 5–6° in latitude at the LGM. The values for regional δ18Ow changes, which were obtained by subtracting the ice volume contribution from the calculated δ18Ow, describe the millennial‐scale water mass migration over the last 30 kyr. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   
10.
The present paper uses planktonic foraminifera and their stable isotopes to study the changes in the depth of thermocline (DOT) in the Okinawa Trough since the last 10000 a based on the analysis of Core B-3GC in the northern Okinawa Trough, together with that of the core in the southern Okinawa Trough. As results show, the thermocline was shallow before 6400 aBP, and deepened afterward, then became shallow again from 4000 to 2000 aBP. The DOT fluctuations display a positive correlation with those of sea surface temperature (SST). In addition, the changes in the northern Okinawa Trough are similar to those in the southern trough, implying a possible connection with the variation of the Kuroshio Current. The changes of SST and DOT suggest that the Kuroshio Current changed its intensity or main axis from 4000 to 2000 aBP and around about 6400 aBP respectively. Moreover, the changes of DOT from 8200 to 6400 aBP may indicate a gradual intensification of the Kuroshio Current.  相似文献   
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