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1.
Sulphur isotopic data for sulphides and barite from several carbonatites (Mountain Pass, Oka, Magnet Cove, Bearpaw Mountains, Phalabora) show that individual carbonatites have different mean sulphide or barite isotopic compositions which deviate from the meteoritic mean δ34S(0‰).Classification of carbonatites in terms of T,?O2 and pH during formation of the sulphur-bearing assemblages indicates that with decreasing T and increasing relative ?O2 the mean δ34S sulphide becomes increasing negative relative to the mean magma δ34S. Only barite-free high temperature carbonatites (Phalabora) in which the mean δ34S sulphide approaches the mean magmaδ34S as a consequence of the paucity of oxidized anionic sulphur species in the magma can be used to directly estimate the mean isotopic composition of the source material.Barites from the Mountain Pass carbonatite show an increase in δ34S with sequence of intrusion of the carbonatite units; dolomitic carbonatite (mean δ34S, + 5.4‰), calcitic carbonatite (+ 4.8%.), silicified carbonatite (+ 6.9‰), tabular carbonatite dikes (+ 8.7‰), mineralized shear zones (+ 9.5‰). Within each of these units a spread of 6.8%. is evident. Isotopic trends in this low temperature (300°C) carbonatite are evaluated by treating the system as a hydrothermal fluid. The observed isotopic variations can be explained by removal of large amounts of sulphur from a fluid whose mean δ34S is 0 to + 1‰  相似文献   

2.
A contemporary probabilistic seismic hazard assessment (PSHA) study for Bulgaria and the surrounding Balkan area is performed under constraints of a newly developed, fit-for-purpose historical earthquake catalogue and the theory of extreme values. Sensitivity analyses are first adopted as preparatory reviews on subsets of the adopted data to determine suitable values for the constraints of cut-off magnitude threshold, sample extreme interval and start year of catalogue data to impose on the parent database for both the full region considered as well as significant urban centres within it. Maximum estimates are then determined for magnitude recurrence hazard using Gumbel’s third asymptotic extreme values distribution for return periods of 50 and 100 years, and also these time intervals at 90 % probability of not being exceeded (PNBE). Gumbel’s first asymptotic extreme values distribution is also used with carefully selected, geographically relevant ground motion models for peak horizontal ground acceleration, PGA(h), and peak horizontal ground velocity, PGV(h), for the same return periods. The former provides direct comparison with the current EUROCODE 8 anti-seismic building code standard promoted across Europe, the previous GSHAP and SESAME hazard mapping projects as well as a number of recent studies. Sofia is forecast an upper bound magnitude of 7.33 M w (±0.78) compared with 7.31 M w (±0.55) for the full Balkan extent and 7.24 M w (±0.70) for the political triple junction area of southwest Bulgaria, viz., Bulgaria, Greece and The Former Yugoslav Republic of Macedonia. Sofia is also forecast a 475-year return period (equivalent to a 50-year return period at 90 % PNBE) magnitude of 7.27 M w, with an equivalent PGA (the standard EUROCODE 8 metric) of 156 cm s?2 and PGV of 13 cm s?1.  相似文献   

3.
Palaeotemperature estimates from the oxygen‐isotope compositions of belemnites have been hampered by not knowing ancient seawater isotope compositions well enough. We have tackled this problem using Mg/Ca as a proxy for temperature and here, we present a ~2 Ma record of paired Mg/Ca and δ18O measurements of Jurassic (Early Pliensbachian) belemnites from the Asturian basin as a palaeo‐proxy of seawater oxygen‐isotope composition. From the combined use of the two approaches, we suggest a δ18Ow composition of about ?0.1‰ for the Jamesoni–Ibex zones. This value may have been increased by about 0.6‰ during the Davoei Zone due to the effect of waters with a different δ18Ow composition. These findings illustrate the inaccuracy of using a globally homogeneous ice‐free value of δ18Ow = ?1‰ for δ18Ocarb‐based palaeotemperature reconstructions. Our data suggest that previous palaeotemperatures calculated in the region from δ18O values of belemnites may have been underestimated as the seawater oxygen isotopic composition could have been higher.  相似文献   

4.
A method for calculating fractional s-character, f s , for TO bonds has been devised to apply to TO4 tetrahedral oxyanions in crystals. These f s -values rank bond lengths with the better correlations obtained for T atoms associated with larger bond strengths and larger electronegativities. As a simple formula, it is found that 2cot2〈?〉3 does a good job of estimating f s where 〈?〉3 is the triple angle average of the three angles common to a given bond.  相似文献   

5.
A workflow is described to estimate specific storage (S s) and hydraulic conductivity (K) from a profile of vibrating wire piezometers embedded into a regional aquitard in Australia. The loading efficiency, compressibility and S s were estimated from pore pressure response to atmospheric pressure changes, and K was estimated from the earliest part of the measurement record following grouting. Results indicate that S s and K were, respectively, 8.8?×?10?6 to 1.2?×?10?5 m?1 and 2?×?10?12 m s?1 for a claystone/siltstone, and 4.3?×?10?6 to 9.6?×?10?6 m?1 and 1?×?10?12 to 5?×?10?12 m s?1 for a thick mudstone. K estimates from the pore pressure response are within one order of magnitude when compared to direct measurement in a laboratory and inverse modelled flux rates determined from natural tracer profiles. Further analysis of the evolution and longevity of the properties of borehole grout (e.g. thermal and chemical effects) may help refine the estimation of formation hydraulic properties using this workflow. However, the convergence of K values illustrates the benefit of multiple lines of evidence to support aquitard characterization. An additional benefit of in situ pore pressure measurement is the generation of long-term data to constrain groundwater flow models, which provides a link between laboratory scale data and the formation scale.  相似文献   

6.
Eighteen basalts and some volcanic gases from the submarine and subaerial parts of Kilauea volcano were analyzed for the concentration and isotope ratios of sulfur. By means of a newly developed technique, sulfide and sulfate sulfur in the basalts were separately but simultaneously determined. The submarine basalt has 700 ± 100 ppm total sulfur with δ34SΣs of 0.7 ± 0.1 ‰. The sulfate/sulfide molar ratio ranges from 0.15 to 0.56 and the fractionation factor between sulfate and sulfide is +7.5 ± 1.5‰. On the other hand, the concentration and δ34SΣs values of the total sulfur in the subaerial basalt are reduced to 150 ± 50 ppm and ?0.8 ± 0.2‰, respectively. The sulfate to sulfide ratio and the fractionation factor between them are also smaller, 0.01 to 0.25 and +3.0‰, respectively. Chemical and isotopic evidence strongly suggests that sulfate and sulfide in the submarine basalt are in chemical and isotopic equilibria with each other at magmatic conditions. Their relative abundance and the isotope fractionation factors may be used to estimate the ?o2 and temperature of these basalts at the time of their extrusion onto the sea floor. The observed change in sulfur chemistry and isotopic ratios from the submarine to subaerial basalts can be interpreted as degassing of the SO2 from basalt thereby depleting sulfate and 34S in basalt.The volcanic sulfur gases, predominantly SO2, from the 1971 and 1974 fissures in Kilauea Crater have δ34S values of 0.8 to 0.9%., slightly heavier than the total sulfur in the submarine basalts and definitely heavier than the subaerial basalts, in accord with the above model. However, the δ34S value of sulfur gases (largely SO2) from Sulfur Bank is 8.0%., implying a secondary origin of the sulfur. The δ34S values of native sulfur deposits at various sites of Kilauea and Mauna Loa volcanos, sulfate ions of four deep wells and hydrogen sulfide from a geothermal well along the east rift zone are also reported. The high δ34S values (+5 to +6%.o) found for the hydrogen sulfide might be an indication of hot basaltseawater reaction beneath the east rift zone.  相似文献   

7.
We tested the effectiveness of stable isotopes as recorders of physiological changes that occur during coral bleaching and recovery. Montipora capitata and Porites compressa fragments were bleached in outdoor tanks with seawater temperature raised to 30 °C (treatment corals) for one month. Additional fragments were maintained at 27 °C in separate tanks (control corals). After one month, (0 months recovery), buoyant weight was measured and a subset of fragments was frozen. Remaining fragments were returned to the reef for recovery. After 1.5, 4, and 8 months, fragments were collected, measured for buoyant weight, and frozen. Fragments were analyzed for stable carbon and oxygen isotopic compositions of the skeleton (δ13Cs; δ18Os) and nitrogen and carbon isotopic compositions of the host tissue (δ15Nh; δ13Ch) and zooxanthellae (δ15Nz; δ13Cz). δ13Cs decreased immediately after bleaching in M. capitata, but not in P. compressa. δ18Os of both species failed to record the warming event. During the remaining months of recovery, δ13Cs and δ18Os were more enriched in treatment than control corals due to decreases in calcification and metabolic fractionation during that time. Increased δ15Nh of treatment P. compressa may be due to expelled zooxanthellae during bleaching and recovery. Increased δ15Nz at 1.5 months in treatment fragments of both species reflects the increased incorporation of dissolved inorganic nitrogen to facilitate mitotic cell division and/or chl a/cell recovery. Changes in δ13Ch and δ13Cz at 1.5 months in treatment M. capitata indicated a large increase in heterotrophically acquired carbon relative to photosynthetically fixed carbon. We experimentally show that isotopes in coral skeleton, host tissue and zooxanthellae can be used to verify physiological changes during bleaching and recovery, but their use as a proxy for past bleaching events in the skeletal record is limited.  相似文献   

8.
The stable isotope content of moisture (δE) removed by evaporation from a well mixed water body with no inflow is related to the isotopic content of the liquid (δ) by the equation m = (δE ? δ)/(δ ? δs). where δs is the isotopic 'steady state' of the liquid for given evaporation conditions, achieved as the liquid volume goes to zero, and m is a measure of the rate of approach of δ to δs. The parameters δs and m can be determined from simple isotopic and volume measurements of liquid water in an evaporation pan. If the mean daily surface water temperatures of such a pan and a nearby lake are equal, then with certain assumptions the pan-derived values of δs and m can be used to calculate δE for the lake surface from a knowledge of the isotopic content of the surface water. The method may be most useful in areas of low rainfall where evaporation pan observations can be conducted over long periods of time without interruption.  相似文献   

9.
In order to understand spatial variations of stable isotope geochemistry in the Quruqtagh basin (northwestern China) in the aftermath of an Ediacaran glaciation, we analyzed carbonate carbon isotopes (δ13Ccarb), carbonate oxygen isotopes (δ18Ocarb), carbonate associated sulfate sulfur (δ34SCAS) and oxygen isotopes (δ18OCAS), and pyrite sulfur isotopes (δ34Spy) of a cap dolostone atop the Ediacaran Hankalchough glacial diamictite at four sections. The four studied sections (YKG, MK, H and ZBS) represent an onshore-offshore transect in the Quruqtagh basin. Our data show a strong paleobathymetry-dependent isotopic gradient. From the onshore to offshore sections, δ13Ccarb values decrease from −2‰ to −16‰ (VPDB), whereas δ18Ocarb values increase from −4‰ to −1‰ (VPDB). Both δ34SCAS and δ34Spy show stratigraphic variations in the two onshore sections (MK and YKG), but are more stable in the two offshore sections (H and ZBS). δ18OCAS values of onshore samples are consistent with terrestrial oxidative weathering of pyrite. We propose that following the Hankalchough glaciation seawater in the Quruqtagh basin was characterized by a strong isotopic gradient. The isotopic data may be interpreted using a three-component mixing model that involves three reservoirs: deep-basin water, surface water, and terrestrial weathering input. In this model, the negative δ13Ccarb values in the offshore sections are related to the upwelling of deep-basin water (where anaerobic oxidation of dissolved organic carbon resulted in 13C-depleted DIC), whereas sulfur isotope variations are strongly controlled by surface water sulfate and terrestrial weathering input derived from oxidative weathering of pyrite. The new data provide evidence for the oceanic oxidation following the Hankalchough glaciation.  相似文献   

10.
The potential to reconstruct paleoclimate from analyses of stable isotopes in fossil leaf cellulose could be enhanced by adequate calibration. This potential is likely to be particularly great in mid-latitude deserts, where a rich store of fossil leaves is available from rodent middens. Trends in δD and δ18O of leaf cellulose were examined for three species growing across climatic gradients caused by elevation and slope aspect in southeastern Utah, USA. The species differed in morphology (Pinus edulis vs. Yucca glauca), photosynthetic pathway (C3Y. glauca vs. CAM Yucca baccata) or both (P. edulis vs. Y. baccata). The δDLCN (leaf cellulose nitrate) and δ18OLC (leaf cellulose) values of P. edulis decreased with elevation. Stem water δD values either increased (in spring) or did not change with elevation (in summer). Needle water δD values usually decreased with elevation and differed greatly with leaf age. These results suggest that δ cellulose values of P. edulis record the effects of climate on the isotopic composition of leaf water but not climate effects on meteoric water. In contrast to P. edulis, δDLCN values of Y. glauca increased with elevation. The δ18OLC values of Y. glauca also increased with elevation but less significantly and only on south-facing slopes. The δ cellulose values in both P. edulis and Y. glauca were most significantly related to changes in temperature, although temperature and precipitation were negatively correlated in the study area. Where all three species co-occurred, their δDLCN values differed but their δ18OLC values were the same. The disparity in δDLCN between Y. baccata and the other species corresponds to differences in biochemical fractionations associated with photosynthetic pathway. Biochemical fractionations may also contribute to differences between the two C3 species. Knowledge of factors affecting responses of individual plant species to environment may be required to infer climate from δDLCN and δ18OLC.  相似文献   

11.
A complete and homogeneous magnitude earthquake catalogue spanning the period 1900 to 2010 was created. The catalogue covers the area 29° to 37.5° N and 39° to 48° E. Entries in the new earthquake catalogue were cross checked and additions made from various sources of earthquake records to ensure that repetitions are not included in this analysis. Events were considered duplicates if they had a time difference of 10 s or less and space origin difference of 0.5° or less. In a given set of duplicate events, an event, which had a magnitude and International Seismological Center source, was retained as the record of the event. The unified magnitude scale, the moment magnitude (M w), was applied throughout the catalogue. The M w for 18 events was reported. The M w for other events was estimated using empirical relations between m b, M s, M L, and M w. Magnitude of completeness, M c, was estimated using the maximum curvature. It was 4.3 M w. Finally, a list of 213 events from 1900 to 2010 with M w?≥?4.3 is presented. The list is considered complete for the period from 1962 to 2010.  相似文献   

12.
Twelve goethite samples with different degrees of substitution of Al for Fe were synthesized at 22-48 °C and pH values of 1.5-14 under closed system conditions and used to study the effects of Al substitution on the hydrogen isotopic fractionation between goethite and its ambient water. The syntheses followed two pathways: (1) Fe3+ hydrolysis in high pH aqueous solutions; (2) oxidation of Fe2+ to Fe3+ in mid to low pH solutions. XRD and SEM analyses indicated that, irrespective of temperature and pH, goethite was the predominant product of the syntheses in all of the experiments (with degrees of Al substitution as high as ∼13 mol %). “High temperature nonstoichiometric” (HTN) water is present in all of the samples and rapidly exchanges D/H with ambient vapor at room temperature. Uncertainties in the value of the apparent D/H fractionation factor (αe-v) between HTN water and ambient exchange water at 22 °C lead to significant uncertainties in determinations of the δD values of structural hydrogen (δDs) in goethites which contain high proportions of HTN water. As determined for the samples of this study, αe-v has a nominal value of 0.942 (±0.02). δDs values determined using an αe-v value of 0.942 indicate that Al substitution increases the δD value of structural hydrogen in goethite by about 1.4 (±0.4)‰ for each increase in Al of 1 mol %. This dependence on Al is of the same sign as, but somewhat larger in magnitude than, the effect of Al predicted by a published model (∼0.7‰ per mol % Al). The overall uncertainties in the current results suggest that an increase of ∼1‰ per mol % Al, as adopted by previous studies, may be a reasonable estimate with which to adjust δ Ds values of natural goethites to those of the pure FeOOH endmember and could be valid for degrees of Al substitution of up to at least 15 mol %. These synthesis experiments also yield a hydrogen isotopic fractionation factor (DαG-W) between pure goethite (α-FeOOH) and liquid water of 0.900 (±0.006), which is analytically indistinguishable from the published value of 0.905 (±0.004). Thus, use of an DαG-W value of 0.905 in applications to the FeOOH component of natural goethites is supported by the current study.  相似文献   

13.
The properties of the source spectra of local shallow-focus earthquakes on Kamchatka in the range of magnitudes M w = 3.5–6.5 are studied using 460 records of S-waves obtained at the PET station. The family of average source spectra is constructed; the spectra are used to study the relationship between M w and the key quasi-dimensionless source parameters: stress drop Δσ and apparent stress σa. It is found that the parameter Δσ is almost stable, while σa grows steadily as the magnitude M w increases, indicating that the similarity is violated. It is known that at sufficiently large M w the similarity hypothesis is approximately valid: both parameters Δσ and σa do not show any noticeable magnitude dependence. It has been established that M w ≈ 5.7 is the threshold value of the magnitude when the change in regimes described occurs for the conditions on Kamchatka.  相似文献   

14.
Oxygen isotope compositions of biogenic phosphates from mammals are widely used as proxies of the isotopic compositions of meteoric waters that are roughly linearly related to the air temperature at high- and mid-latitudes. An oxygen isotope fractionation equation was determined by using present-day European arvicoline (rodents) tooth phosphate: δ18Op = 20.98(±0.59) + 0.572(±0.065) δ18Ow. This fractionation equation was applied to the Late Pleistocene karstic sequence of Gigny, French Jura. Comparison between the oxygen isotope compositions of arvicoline tooth phosphate and Greenland ice core records suggests to reconsider the previously established hypothetical chronology of the sequence. According to the δ18O value of meteoric water-mean air temperature relationships, the δ18O value of arvicoline teeth records variations in mean air temperatures that range from 0° to 15°C.  相似文献   

15.
XANES analyses at the sulfur K-edge were used to determine the oxidation state of S species in natural and synthetic basaltic glasses and to constrain the fO2 conditions for the transition from sulfide (S2−) to sulfate (S6+) in silicate melts. XANES spectra of basaltic samples from the Galapagos spreading center, the Juan de Fuca ridge and the Lau Basin showed a dominant broad peak at 2476.8 eV, similar to the spectra obtained from synthetic sulfide-saturated basalts and pyrrhotite. An additional sharp peak at 2469.8 eV, similar to that of crystalline sulfides, was present in synthetic glasses quenched from hydrous melts but absent in anhydrous glasses and may indicate differences in sulfide species with hydration or presence of minute sulfide inclusions exsolved during quenching. The XANES spectra of a basalt from the 1991 eruption of Mount Pinatubo, Philippines, and absarokitic basalts from the Cascades Range, Oregon, USA, showed a sharp peak at 2482.8 eV, characteristic of synthetic sulfate-saturated basaltic glasses and crystalline sulfate-bearing minerals such as hauyne. Basaltic samples from the Lamont Seamount, the early submarine phase of Kilauea volcano and the Loihi Seamount showed unequivocal evidence of the coexistence of S2− and S6+ species, emphasizing the relevance of S6+ to these systems. XANES spectra of basaltic glasses synthesized in internally-heated pressure vessels and equilibrated at fO2 ranging from FMQ − 1.4 to FMQ + 2.7 showed systematic changes in the features related to S2− and S6+ with changes in fO2. No significant features related to sulfite (S4+) species were observed. These results were used to construct a function that allows estimates of S6+/ΣS from XANES data. Comparison of S6+/ΣS data obtained by S Kα shifts measured with electron probe microanalysis (EPMA), S6+/ΣS obtained from XANES spectra, and theoretical considerations show that data obtained from EPMA measurements underestimate S6+/ΣS in samples that are sulfate-dominated (most likely because of photo-reduction effects during analysis) whereas S6+/ΣS from XANES provide a close match to the expected theoretical values. The XANES-derived relationship for S6+/ΣS as a function of fO2 indicates that the transition from S2− to S6− with increasing fO2 occurs over a narrower interval than what is predicted by the EPMA-derived relationship. The implications for natural systems is that small variation of fO2 above FMQ + 1 will have a large effect on S behavior in basaltic systems, in particular regarding the amount of S that can be transported by basaltic melts before sulfide saturation can occur.  相似文献   

16.
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17.
This study was conducted in six plots along an elevation gradient in the Qinghai spruce (Picea crassifolia Kom.) forest ecosystem of the Qilian Mountains, northwest China. Soil CO2 efflux over bare soil (R s) and moss covered soil (R s+m) were investigated from June to September in 2010 and 2011 by means of an automated soil CO2 flux system (LI-8100). The results showed that R s ranged from 1.51 to 3.96 (mean 2.64 ± 0.72) μmol m?2 s?1 for 2010, and from 1.41 to 4.09 (mean 2.55 ± 0.70) μmol m?2 s?1 for 2011. The daily change trend of R s resembled that of air temperature (T a), and there was a hysteresis between R s and soil temperature (T s). The seasonal variations of R s at lowlands (i.e., Plot 1, Plot 2 and Plot 3) were driven by soil moisture and temperature (T a and T s), while that at highlands (i.e., Plot 4, Plot 5 and Plot 6) were obviously affected by temperature. There were higher values at Plot 2 and Plot 6, which were caused by the interaction between soil moisture and temperature. In addition, soil CO2 efflux over moss covered soil (R s+m) was 8.83 % less than that over bare soil (R s), indicating that moss was another factor affecting R s. It was concluded that R s had temporal and spatial variations and was mainly controlled by temperature and soil moisture; the main determinants differed at different elevations; moss could reduce R s.  相似文献   

18.
This study investigates how estimates of uranium endowment made by a geologist using an appraisal system that is based upon a formalization of geoscience and decision rules compare with estimates made by informal and unconstrained intuitive processes. The motivation for this study derives from the premise that formalization of decisions would mitigate the heuristic biases and hedging that may result from the use of unconstrained intuitive processes. Estimates of the uranium endowment of the San Juan Basin of New Mexico by four methodologies are compared in this study. These methods, ranked from top to bottom by degree of decomposition (mitigating of heuristic bias)and control on hedging, are as follows Implicit 2 1.5 × 106 s.t. of U3O8 Implicit 1 1.6 × 106 s.t. of U3O8 NURE (1980) 2.4 × 106 s.t. of U3O8 Appraisal system 3.9 × 106 s.t. of U3O8 The magnitude of expected uranium endowment estimated by these methods, ranked from smallest to largest, is in this same order. With the exception of the NURE estimates, the magnitude of the variance (uncertainty)of uranium endowment, ranked from smallest to largest, also is in this same order. These results prompt the suggestion that the more decomposed and formalized the estimation procedure, the greater the expected value and the variance of uranium endowment. Equivalently, predicating U 3 O 8 endowment estimation strictly upon that part of the geologist's geoscience that is useful in making U 3 O 8 endowment estimates and upon his understanding of the region's history produced larger estimates than have previously been reported. However, this method of estimation also shows that uncertainty about the actual state of U 3 O 8 endowment is much greater than previously described.  相似文献   

19.
The build up of the isotopic signal in corals was followed by sampling the newly formed skeleton at a monthly resolution for a period of two years in order to establish the interrelations between the calcification processes and the skeletal isotopic composition. We deployed two underwater sampling schemes, which provide a monitor of the changes in water temperature and δ18O and in the corresponding newly accreted skeleton of undisturbed Porites lutea colonies under natural conditions and four transplanted colonies, which maintained the genetic identity throughout the experiment. The results indicate that δ18O of the newly accreted skeleton does not correlate with ambient temperature although the seasonal temperature variability at the site (winter to summer) is in the order of 6 °C and δ18O of seawater is constant throughout the year. In contrast to the newly formed surface skeleton, the isotopic compositions of the deep and older parts of the skeleton show the predicted annual isotopic pattern with highly significant correlation between δ18Os and SST. The transformation between temperature-independent to temperature-dependent isotopic signal occurs several months after the skeleton was formed at the surface. The position of the skeleton in relation to the open sea may generate the difference between δ18Os of the surface skeleton and that of the skeleton previously accreted further down the tissue layer. Our data support the general model of a multi-step skeletogenesis process, where the temperature independent skeleton is entails the first step, the production of skeletal scaffold, and the environmental temperature signature is captured by the next two other steps: the thickening and the periodic abrupt uplift occurring at the depth of the tissue layer. However, re-examination and development of the current isotopic models for coral calcification are required in order to explain the observed different temperature dependency during the growth’s sequence.  相似文献   

20.
Benthic and planktonic oxygen isotope (δ18Occ) and Mg/Ca analyses in two cores from the Northeast Atlantic have permitted the reconstruction of surface- and deep-water temperature (Tdw) and δ18O (δ18Ow) variations across the last two deglaciations. These records allow the timing of de-glacial melt-water pulses reaching the Northeast Atlantic to be compared with the evolution of local deep-water Tdw–δ18Ow conditions. Although each glacial termination is unique in detail, a similar pattern of hydrographic change is reconstructed for both deglaciations, with the first major decrease in deep-water δ18Ow (due to sea-level and/or purely local deep-water change) occurring in parallel with the onset of intensely cold glacial surface-water temperatures, and prior to a ‘terminal’ ice-rafting and melt-water event. The evolution of deep-water across both de-glaciations involved two transient incursions of cold, low-δ18O water into the deep Northeast Atlantic, the second of which was particularly pronounced each time. These pulses of cold deep-water are interpreted to reflect the incursion of water directly analogous to modern Antarctic Bottom Water (AABW), and containing a significant component of brine rejected during sea-ice formation. The results presented here show that the same type of transient changes in deep-water circulation that occurred across Termination I also occurred across Termination II, and that as a result of these deep-ocean changes, the timing of each benthic δ18O ‘termination’ cannot precisely reflect the timing of de-glacial sea-level change, as many palaeoceanographic interpretations (and some controversies) are prone to assume. Such ‘imprecision’ (in timing especially) may well extend to marine isotope stage (MIS) boundaries in general, as a principle of hydrographic variability and its expression in the geological record.  相似文献   

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