首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到5条相似文献,搜索用时 15 毫秒
1.
We present three new benthic foraminiferal δ13C, δ18O, and total organic carbon time series from the eastern Atlantic sector of the Southern Ocean between 41°S and 47°S. The measured glacial δ13C values belong to the lowest hitherto reported. We demonstrate a coincidence between depleted late Holocene (LH) δ13C values and positions of sites relative to ocean surface productivity. A correction of +0.3 to +0.4 [‰ VPDB] for a productivity-induced depletion of Last Glacial Maximum (LGM) benthic δ13C values of these cores is suggested. The new data are compiled with published data from 13 sediment cores from the eastern Atlantic Ocean between 19°S and 47°S, and the regional deep and bottom water circulation is reconstructed for LH (4–0 ka) and LGM (22–16 ka) times. This extends earlier eastern Atlantic-wide synoptic reconstructions which suffered from the lack of data south of 20°S. A conceptual model of LGM deep-water circulation is discussed that, after correction of southernmost cores below the Antarctic Circumpolar Current (ACC) for a productivity-induced artifact, suggests a reduced formation of both North Atlantic Deep Water in the northern Atlantic and bottom water in the southwestern Weddell Sea. This reduction was compensated for by the formation of deep water in the zone of extended winter sea-ice coverage at the northern rim of the Weddell Sea, where air–sea gas exchange was reduced. This shift from LGM deep-water formation in the region south of the ACC to Holocene bottom water formation in the southwestern Weddell Sea, can explain lower preformed δ13CDIC values of glacial circumantarctic deep water of approximately 0.3‰ to 0.4‰. Our reconstruction brings Atlantic and Southern Ocean δ13C and Cd/Ca data into better agreement, but is in conflict, however, with a scenario of an essentially unchanged thermohaline deep circulation on a global scale. Benthic δ18O-derived LGM bottom water temperatures, by 1.9°C and 0.3°C lower than during the LH at deepest southern and shallowest northern sites, respectively, agree with the here proposed reconstruction of deep-water circulation in the eastern South Atlantic Ocean.  相似文献   

2.
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   

3.
Owing to the very gently sloping nature of the flood plain in the lower White Nile valley, which is underlain by a former lake-bed, the depositional record in that area is unusually well preserved. In Egypt and along the Blue Nile phases of erosion have destroyed segments of the sedimentary record, but the White Nile sequence is a good proxy for both the main Nile and the Blue Nile. During the last 15 ka, at least, times of high flow in the Blue Nile and main Nile were synchronous with those in the White Nile.Not all the White Nile flood deposits have been preserved but calibrated radiocarbon dates obtained on fossil freshwater and amphibious Pila shells and fish bones indicate that White Nile levels were high around 14.7–13.1 ka, 9.7–9.0 ka, 7.9–7.6 ka, 6.3 ka and 3.2–2.8 ka. The Blue Nile record is more fragmentary and that of the main Nile even more so except for the Holocene Nile delta. Calibrated radiocarbon ages for high Blue Nile flows indicate very high flood levels towards 13.9–13.2 ka, 8.6 ka, 7.7 ka and 6.3 ka.Incision by the Blue Nile and main Nile has caused progressive incision in the White Nile amounting to at least 4 m since the terminal Pleistocene  15 ka ago and at least 2 m over the past 9 ka. The Blue Nile seems to have cut down at least 10 m since  15 ka and at least 4 m since 9 ka. The time-transgressive and relatively late inception of plant domestication in the Nile valley may partly reflect this history of incision. Nile incision would propagate upstream into the White Nile valley, draining previously swampy areas along the valley floor, which would then become accessible to cultivation.  相似文献   

4.
Hydrographic changes in the NW Arabian Sea are mainly controlled by the monsoon system. This results in a strong seasonal and vertical gradient in surface water properties, such as temperature, nutrients, carbonate chemistry and the isotopic composition of dissolved inorganic carbon (δ13CDIC). Living specimens of the planktic foraminifer species Globigerina bulloides and Globigerinoides ruber, were collected using depth stratified plankton tows during the SW monsoon upwelling period in August 1992 and the NE monsoon non-upwelling period in March 1993. We compare their distribution and the stable isotope composition to the seawater properties of the two contrasting monsoon seasons. The oxygen isotope composition of the shells (δ18Oshell) and vertical shell concentration profiles indicate that the depth habitat for both species is shallower during upwelling (SW monsoon period) than during non-upwelling (NE monsoon period). The calcification temperatures suggest that most of the calcite is precipitated at a depth level just below the deep chlorophyll maximum (DCM), however above the main thermocline. Consequently, the average calcification temperature of G. ruber and G. bulloides is lower than the sea surface temperature by 1.7±0.8 and 1.3±0.9 °C, respectively. The carbon isotope composition of the shells (δ13Cshell) of both species differs from the in situ δ13CDIC found at the calcification depths of the specimens. The observed offset between the δ13Cshell and the ambient δ13CDIC results from (1) metabolic/ontogenetic effects, (2) the carbonate chemistry of the seawater and, for symbiotic G. ruber, (3) the possible effect of symbionts or symbiont activity. Ontogenetic effects produce size trends in Δδ13Cshell–DIC and Δδ18Oshell–w: large shells of G. bulloides (250–355μm) are 0.33‰ (δ13C) and 0.23‰ (δ18O) higher compared to smaller ones (150–250 μm). For G. ruber, this is 0.39‰ (δ13C) and 0.17‰ (δ18O). Our field study shows that the δ13Cshell decreases as a result of lower δ13CDIC values in upwelled waters, while the effects of the carbonate system and/or temperature act in an opposite direction and increase the δ13Cshell as a result lower [CO32−] (or pH) values and/or lower temperature. The Δδ13Cshell–DIC [CO32−] slopes from our field data are close to those reported literature from laboratory culture experiments. Since seawater carbonate chemistry affects the δ13Cshell in an opposite sense, and often with a larger magnitude, than the change related to productivity (i.e. δ13CDIC), higher δ13Cshell values may be expected during periods of upwelling.  相似文献   

5.
A review of all available amino acid racemization D (alloisoleucine)/L (isoleucine) data from the whole shell of four molluscan species from Late and late Middle Pleistocene deposits of the Netherlands is presented. The data allow the distinction of 5 aminostratigraphical units, NAZ (Netherlands Amino Zone) A–E, each representing a temperate stage. The zones are correlated with marine isotope stages 1, 5e, 7, 9, and 11 respectively. Apart from NAZ-D (MIS 9), in all aminozones the marine transgression reached the present-day onshore area of the Netherlands. The transgression during NAZ-C (Oostermeer Interglacial: MIS 7) seems to be at least as widespread as its counterpart during NAZ-B (Eemian: MIS 5e) in the southern bight of the North Sea Basin. The stratigraphic position of the Oostermeer Interglacial is just below deposits of the Drente phase of the Saalian and because of this position the interglacial marine deposits have formerly erroneously considered to be of Holsteinian age. Neede, the ‘classic’ Dutch Holsteinian site, is dated in NAZ-E (MIS 11), like Noordbergum. Although the validity of these zones has been checked with independent data, some overlap between succeeding zones may occur. The relation between amino acid data from elsewhere in the North Sea Basin and the Netherlands amino zonation is discussed. The deposits at the Holsteinian stratotype Hummelsbüttel in North West Germany are dated in NAZ-D. This interglacial correlates with MIS 9. The Belvédère Interglacial, which is of importance for its archaeology, is in NAZ-D (MIS 9) and therefore of Holsteinian age as well. The lacustroglacial ‘pottery clays’ in the Noordbergum area are deposits from two glacial stages, which can be correlated with MIS 8 and 10 (the Elsterian). The pottery clay that is considered equivalent to the German ‘Lauenburger Ton’ correlates with MIS 10.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号