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1.
Molar ratios of Mg/Ca and Sr/Ca were measured in two species of ostracod shells preserved in the upper core (15-55 m) of the Heqing Basin in Yunnan Province, southwest China. By correlating the molar ratios between Mg/Ca and Sr/Ca and comparing them with Sr concentrations of the sediments, we suggested that: (1) the molar Mg/Ca and Sr/Ca ratio variations in respective ostracod primo re- flected the changes in its ambient water composition and ecology; (2) the molar Sr/Ca ratios responded better to the salinity change linearly than Mg/Ca without aragonite precipitation in the system, and otherwise there was no linear relation between them; and (3) the molar Sr/Ca ratios were mainly con- trolled by salinity and authigenic carbonate precipitation, whereas the molar Mg/Ca ratios were related to both salinity and temperature. In fact, the rate of ostracod growth owing to temperature controls the fluctuation of Mg/Ca in shells. Here, more attentions should be paid to the constraint of authigenic mineral precipitation processes on the trace elements in ostracod shells and to the correlation between these trace elements in biogenic carbonates and compositions of the sediments in systems and in fu- ture in vitro experiments. 相似文献
2.
XIAO YingKai LIU WeiGuo MA YunQi ZHANG YanLing HE MaoYong LUO ChongGuang LIAO QingQiang 《中国科学:地球科学(英文版)》2014,57(5):1048-1060
To be used as proxies of seawater surface temperature(SST), the δ 18Oc values and Sr/Ca and Mg/Ca ratios of scleractinian coral skeletons must be verified by coral culture experiments in the laboratory. This paper describes a coral culture experiment that was conducted at several seawater temperatures T(21–28°C) using a tandem aquarium system and the new method for depositing coral skeletons grown under controlled conditions. The δ 18Oc values and the Sr/Ca and Mg/Ca ratios of the cultured coral were measured. We concluded that the δ 18Oc values and Sr/Ca and Mg/Ca ratios of the cultured coral are clearly correlated with T. The linear regression curve is δ18Oc(‰)=δ0.1427δT(°C)δ0.1495(n=18, r=0.955, p0.0001), and the slope of δ0.1427‰/°C is at the low end of the range of published values(δ0.13–δ0.29‰/°C). The Sr/Ca ratio decreases with increasing T, whereas the Mg/Ca ratio increases with increasing T, indicating a negative correlation between Sr/Ca and Mg/Ca. Their linear regression curves are Sr/Ca(mmol/mol)=δ0.04156δT+10.59(n=15, r=0.789, p0.005) and Mg/Ca(mmol/mol)= 0.04974δT+2.339(n=17, r=0.457, p0.05), respectively, which demonstrate that when Mg/Ca and Sr/Ca are increased by one unit, T increases by 5.19°C and decreases by 15.62°C, respectively. These variations are significantly lower than published values. 相似文献
3.
J.E. Ferguson G.M. Henderson M. Kucera R.E.M. Rickaby 《Earth and Planetary Science Letters》2008,265(1-2):153-166
The Mg/Ca ratio of foraminiferal calcite is an important proxy for estimating past ocean temperatures. Used in conjunction with δ18O of foraminiferal calcite it allows deconvolution of temperature and ice-volume signals to infer past ocean temperatures and salinities (assuming the relationship between seawater δ18O and salinity is known). Such work assumes that temperature is the only, or at least the dominant, environmental controller of foraminiferal Mg/Ca. The semi-enclosed Mediterranean Sea, where salinity varies from 36 to 40 psu over a seasonal temperature range of between only 5 °C to 8 °C, provides a relevant setting to test this assumption outside the laboratory. In this study, planktonic foraminifera (O. universa, G. siphonifera, G. bulloides and G. ruber (white) and (pink)) were picked from 11 box core tops spanning the Mediterranean salinity gradient and analysed for their trace-element concentrations. Mg/Ca ratios are higher, for the associated calcification temperatures, than in other regions where calibrations have been conducted and correlate poorly with calcification temperature. Mg/Ca ratios are particularly high for samples from the Eastern Mediterranean where salinity is unusually high. Correlations of Mg/Ca with the calcification salinity are statistically significant with Mg/Ca changing by 15–59% per psu, suggesting that salinity may act as a control on Mg/Ca ratios in addition to the dominant temperature control. We show that contamination by non-carbonate material and diagenetic high-Mg carbonate overgrowths cannot account for the observed trend of increasing Mg/Ca with salinity. A relationship between Mg/Ca and salinity is also suggested by re-analysis of calibrations from open-ocean settings. These new Mediterranean results are from a region with unusually high salinity but suggest that the effects of salinity on the Mg/Ca palaeothermometer should be considered even in open-ocean settings, particularly where large salinity changes occurred in the past. 相似文献
4.
Discharge from karst springs contains a mixture of conduit and matrix water, but the variations in groundwater mixing are poorly known. Storm events present an opportunity to try to map flow components because water entering during storms is more dilute and provides a tracer as it mixes with pre‐event water along the flowpath from the recharge area to discharge at a spring. We used hysteresis plots of Mg/Ca ratios in a spring in the Cumberland Valley of Pennsylvania to map conduit (higher Ca) vs. diffuse (higher Mg) sources of recharge. We observed two types of temporal heterogeneity: within a storm event and from storm to storm. The timing of the variation in Mg/Ca suggested sources of mixing waters. An increase in the Mg/Ca ratio at the beginning of some storms while conductivity declined suggested diffuse recharge through the epikarst. The rapid changes in Mg/Ca ratios for low‐intensity events probably occurred as the rainfall waxed and waned and illustrate that a variety of flowpaths are available at this spring because additional flushing of Mg occurred. In contrast, the conductivity hysteresis began with dilute water initially and rotation was similar from storm to storm. Hysteresis plots of the Mg/Ca ratio have the potential of revealing more of the complexity in discharge than conductivity alone. A better understanding of flow components in karst is needed to protect these aquifers as a groundwater resource. 相似文献
5.
Chuan-Chou Shen David W. Hastings Typhoon Lee Chin-Hsin Chiu Meng-Yang Lee Kuo-Yen Wei R. Lawrence Edwards 《Earth and Planetary Science Letters》2001,190(3-4):197-209
Glacial–interglacial variation in the marine Sr/Ca ratio has important implications for coral Sr thermometry [J.W. Beck et al., Science 257 (1992) 644–647]. A possible variation of 1–3% was proposed based on ocean models [H.M. Stoll and D.P. Schrag, Geochim. Cosmochim. Acta 62 (1998) 1107–1118]. Subsequently, studies have used fossil foraminifera to test this prediction [P.A. Martin et al., Geochem. Geophys. Geosyst. 1 (1999); H.M. Stoll et al., Geochim. Cosmochim. Acta 63 (1999) 3535–3547; H. Elderfield et al., Geochem. Geophys. Geosyst. 1 (2000)]. But whether some component of foraminiferal Sr/Ca variation can be uniquely ascribed to seawater Sr variation is still not clear. To address this question, we developed cleaning and analysis techniques and measured Sr/Ca ratios on individual shells of the modern benthic foraminifer Cibicidoides wuellerstorfi. We showed that different size shells have different Sr/Ca ratios; however, samples with shell sizes of 355–500 μm appear to have normally distributed Sr/Ca ratios (1σ=1.8%). For multi-shell measurements (with estimated errors of 0.12–0.39%), the ratio varied by as much as 7.2±0.5% during the last glaciation for two Caribbean records at the same site and by 3.7±0.5% over the past 40,000 yr for one record from the Sierra Leone Rise in the eastern equatorial Atlantic. The two Caribbean records are very similar indicating that the behavior of shell Sr uptake was identical locally and that the shell Sr/Ca ratio faithfully reflects the local environment. The Atlantic record differs from the Caribbean records by as much as several percent. Thus, the foraminiferal Sr/Ca changes cannot be solely due to changes in seawater Sr/Ca unless the glacial deep ocean had spatial variation in Sr/Ca well in excess of the modern ocean. Certain similarities between the three records do exist. Notably, the rate of change of Sr/Ca is similar between 9 and 0 ka (−0.25%/kyr) and between 25 and 16 ka (+0.16%/kyr). This suggests that during these intervals, benthic foraminiferal Sr/Ca was affected by similar large-scale variables. One of these variables may be the average marine Sr/Ca ratio; however, comparison with model predictions [H.M. Stoll and D.P. Schrag, Geochim. Cosmochim. Acta 62 (1998) 1107–1118] suggests other factors must also be considered. The discrepancies between the two sites may be related to the different water mass histories for the Caribbean and eastern Atlantic. Our results suggest that variation of the seawater Sr budget only partially contributed to C. wuellerstorfi Sr/Ca records, while other significant factors still need to be quantified. At present we cannot confidently determine past seawater Sr/Ca variation from our foraminiferal records. 相似文献
6.
Controls on shell Mg/Ca and Sr/Ca in cultured planktonic foraminiferan, Globigerinoides ruber (white) 总被引:2,自引:0,他引:2
B. Ksakürek A. Eisenhauer F. Bhm D. Garbe-Schnberg J. Erez 《Earth and Planetary Science Letters》2008,273(3-4):260-269
Mg/Ca and Sr/Ca ratios were determined on a single species of planktonic foraminiferan, Globigerinoides ruber (white), collected from the Gulf of Eilat and cultured in seawater at five different salinities (32 to 44), five temperatures (18 to 30 °C) and four pH values (7.9 to 8.4). The Mg/Ca-temperature calibration of cultured G. ruber (with an exponential slope of 8 ± 3%/°C) agrees well with previously published calibrations from core-tops and sediment traps. However, the dependence of Mg/Ca on salinity (with an exponential slope of 5 ± 3%/psu) is also significant and should be included in the calibration equation. With this purpose, we calculated a calibration equation for G. ruber dependent on both temperature and salinity within the 95% confidence limits:
Mg/Ca(mmol/mol)=exp[0.06(±0.02)*S(psu)+0.08(±0.02)*T(°C)−2.8(±1.0)],R2=0.95