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1.
Most of the petrologic data available for Type B inclusions comes from Type B1s. Relatively little comes from the B2s, and there has not been a systematic comparison of the properties of their two most abundant minerals. In this work, we document the compositions and zoning patterns of melilite and fassaite in Type B2 inclusions, and compare and contrast them with the features of their counterparts in Type B1 inclusions. We find that melilite compositions in Type B2 inclusions are similar to those of Type B1s, with maximum Åk contents of ∼75 mol % and a positive correlation between Åk and Na2O contents. Asymmetrically zoned melilite is common in Type B2s as are melilite grains with reversely zoned regions, and the reversely zoned portions of crystals are thicker than in B1s. In B2s, like B1s, fassaite is zoned with decreasing Ti, Sc, and V oxide contents from cores to rims of grains. Approximately half of the Ti is trivalent, but unlike that in B1s, within fassaite grains in B2s the Ti3+/(Ti3+ + Ti4+) ratio does not decrease from core to rim, and sharp enrichments (“spikes”) in Ti3+ and V are not observed. Sector-zoned fassaite is much more common in B2s than in B1s. The differences we observed can be accounted for by the differences in bulk compositions between B1s and B2s. Type B2 inclusions tend to have higher SiO2 contents, hence higher An/Ge component ratios, than Type B1s. Phase equilibria show that, compared to B1s, in B2s less melilite should crystallize prior to the appearance of fassaite, so that in B2s a higher proportion of melilite cocrystallizes with fassaite, causing more of the crystals to be reversely zoned; more melilite crystallizes while adjacent to other crystals, leading to asymmetrical zoning; and with more liquid available, transport of components to growing fassaite occurs more readily than in B1s, facilitating crystal growth and giving rise to sector zoning. The lack of zoning with respect to Ti3+/Titot and the absence of Ti3+-, V-rich spikes suggest that Type B2 melts maintained equilibrium with the nebular gas throughout crystallization, while the interiors of B1s were probably isolated from the gas, perhaps by their melilite mantles. This makes the similarity of Na-Åk relationships in B1 and B2 melilite difficult to understand, but apparently enclosure by melilite mantles was not necessary for the retention of Na2O during crystallization of Type B refractory inclusions.  相似文献   

2.
Large variations are reported in the B concentrations and isotopic ratios of river and thermal spring waters in Guadeloupe, Lesser Antilles. Rivers have δ11B values around 40‰ and B concentrations lower than 30 μg/L, while thermal springs have δ11B of 8–15‰ and B concentrations of 250–1000 μg/L. River samples strongly impacted by hydrothermal inputs have intermediate δ11B and B contents. None of these surface water samples have δ11B comparable to the local unweathered volcanic rocks (around 0‰), implying that a huge isotopic fractionation of 40‰ takes place during rock weathering, which could be explained by preferential incorporation of 10B during secondary mineral formation and adsorption on clays, during rock weathering or in the soils. The soil-vegetation B cycle could also be a cause for such a fractionation. Atmospheric B with δ11B of 45‰ represents 25–95% of the river B content. The variety of the thermal spring chemical composition renders the understanding of B behavior in Guadeloupe hydrothermal system quite difficult. Complementary geochemical tracers would be helpful.  相似文献   

3.
The investigation is based on diatem- and pollen analyses of a main profile from the ancient lagoon Barsebäcksmossen. The chronology is bared on C14--dating.
Seven transgressions are indicated, viz. 5200–4800 B.C., 4600–4400 R.C., 4150–3900 B.C., 3800–3700 B.C., 3600–3500 B.C., 3100–2950 H.C. and 2050–1850 B.C. Thc trangressions 4150–3900 B.C., 3800–3700 B.C. and 3600–3500 B.C. may only represent fluctuations during a 'complex' transgresssion. The transgresssion in Barsebäcksmtrssen are correlated with the transgresssion established by Berglund in the Baltic Sea and by Mörner in the Kattegatt sea.
A change in the date of the pollen-zone boundary AT 1/AT 2 from 4500–4600 B.C. to 5200 B.C. is proposed.  相似文献   

4.
Great earthquakes of variable magnitude at the Cascadia subduction zone   总被引：1，自引：0，他引：1  
Comparison of histories of great earthquakes and accompanying tsunamis at eight coastal sites suggests plate-boundary ruptures of varying length, implying great earthquakes of variable magnitude at the Cascadia subduction zone. Inference of rupture length relies on degree of overlap on radiocarbon age ranges for earthquakes and tsunamis, and relative amounts of coseismic subsidence and heights of tsunamis. Written records of a tsunami in Japan provide the most conclusive evidence for rupture of much of the plate boundary during the earthquake of 26 January 1700. Cascadia stratigraphic evidence dating from about 1600 cal yr B.P., similar to that for the 1700 earthquake, implies a similarly long rupture with substantial subsidence and a high tsunami. Correlations are consistent with other long ruptures about 1350 cal yr B.P., 2500 cal yr B.P., 3400 cal yr B.P., 3800 cal yr B.P., 4400 cal yr B.P., and 4900 cal yr B.P. A rupture about 700-1100 cal yr B.P. was limited to the northern and central parts of the subduction zone, and a northern rupture about 2900 cal yr B.P. may have been similarly limited. Times of probable short ruptures in southern Cascadia include about 1100 cal yr B.P., 1700 cal yr B.P., 3200 cal yr B.P., 4200 cal yr B.P., 4600 cal yr B.P., and 4700 cal yr B.P. Rupture patterns suggest that the plate boundary in northern Cascadia usually breaks in long ruptures during the greatest earthquakes. Ruptures in southernmost Cascadia vary in length and recurrence intervals more than ruptures in northern Cascadia.  相似文献   

5.
An analytical procedure has been developed to measure in situ the 11 B/10 B ratio in terrestrial basaltic rocks and meteoritic chondrules having B concentration of less than 1 μg g?1 using a small radius ims3f ion microprobe. The central difficulties for these measurements are (i) the removal of the trace amount of B contamination introduced in the sample during polishing, (ii) the precise calibration of instrumental mass fractionation of B isotopes and (iii) the low count rates of 10 B and 11 B. Contamination experiments conducted with isotopically labelled B enriched in 10 B showed that ultrasonic cleaning in bi-distilled water (< 1 ng g?1 B) and pre-sputtering of the analysed area decrease B contamination to the level of 0.01 μg g?1. Analyses of isotope standards spanning a range of 11 B/10 B between 3.93 and 4.20 showed that instrumental mass fractionation was constant within? during one session of analyses. Repeated analyses of a standard glass showed a reproducibility of instrumental mass fractionation between February 1991 and October 1996 of 1.3. Taking into account all sources of error, boron isotope measurements are accurate to within 5 for meteoritic samples having B contents in the range 0.1 to 1 μg g?1. A slightly better accuracy of 1.5 can be achieved for basaltic glasses which can be sputtered with very intense primary beams.  相似文献   

6.
In order to test the potential of B isotopes as a tracer of contamination of the atmosphere, the B isotopic composition of rainwater samples monitored over a year in the centre of Paris, France were determined. Boron concentrations range from 19 nmol/L to 500 nmol/L and δ11B range from 0‰ to +38‰. Mean annual values are 148 nmol/L and +25‰, respectively. The results suggest that variability in B isotopic compositions is mainly caused by mixing of two main sources, although isotopic fractionation during the evaporation–condensation processes may also be important. One source is a marine component, which exhibits a heavy B isotopic composition. The decrease of δ11B in rainwater with increasing NO3/B and SO4/B molar ratios suggests that a second source may be anthropogenic emissions. To constrain this end-member, B was determined in urban particulates, which were enriched in the light isotope and the lowest values were consistent with a B-rich fossil fuel composition. These results confirm the great sensitivity of B to anthropogenic sources and the ability of B isotopic ratios to decipher the origin of B in the atmosphere.  相似文献   

7.
We have analyzed B in carbonaceous chondrites in order to clarify a factor of 100 difference between the solar system B abundance derived from the solar photosphere and that inferred from previous meteorite data. Consistent results were obtained from two instrumental methods for B analysis: (a) counting of the high energy betas from 12B produced by the 11B(d,p) reaction, and (b) measurement of particle track densities from 10B(n,α)7Li in a plastic track detector affixed to a homogenized meteorite sample. Contamination is a major problem in B analyses, but extensive testing showed that our results were not seriously affected. Our B concentrations are typically 1–2 ppm and are a factor of 2–6 lower than previous carbonaceous chondrite measurements. Our data for the Cl chondrites Ivuna and Orgueil would indicate a solar system B/Si atomic abundance ratio of 58 × 10?6, but this is still a factor of 2–10 higher than the photospheric estimates. It may be that B is depleted in the sun by thermonuclear processes; however, the similarity of photospheric and meteoritic Be abundances is a problem for this point of view. Alternatively, B may be enhanced in carbonaceous chondrites, but this would make B a cosmochemically unique element. A mm-sized (Fe,Mn,Mg)CO3 crystal from Orgueil shows no B enrichment. We find 10B ≤ 1016 atoms/g in two Allende fine-grained inclusions suggesting that B is not a refractory element under solar nebula conditions. This 10B limit, when taken as a limit on 10Be when the inclusion formed, puts constraints on the possibility of a solar system synthesis of 26Al. For a proton spectrum of E?a, a must be ≥ 3 if a solar gas is irradiated or a ≥1.5 if dust of solar composition is irradiated.  相似文献   

8.
11B/10B ratios of the high temperature fumarolic gases (>465°C) of this island were found to be constant within the limits of experimental error (11B/10B = 4.066). This value may represent the 11B/10B ratio of boron in the andesite magma. 11B/10B ratios of the low temperature fumarolic gases (<235°C) were found to vary from 4.053 to 4.077. 11B/10B ratios of some sassolites were approximately equal to that of the fumarolic condensates and the other ones were slightly enriched in 10B compared to the fumarolic condensates.  相似文献   

9.
Li  Bin-Kai  He  Mao-Yong  Ma  Hai-Zhou  Cheng  Huai-De  Ji  Lian-Min 《中国地球化学学报》2022,41(5):731-740

Boron is an essential, widely used, micronutrient element and is abundant in salt lakes on the Qinghai-Tibet Plateau. The origin and distribution of boron brine deposits on the Qinghai-Tibet Plateau is an important foundation for B resource formation, evolution, and enrichment, which have long been the subject of debate. The boron isotope system is a sensitive geochemical tracer, making it useful for effectively and precisely tracking a wide range of geological processes and sources. This study investigates the major cations, [B], and δ11B values of samples (lake brine, river waters, and cold spring water) from the Bangor Co Lake which is a typical salt lake rich in boron in Tibet, China. There are magnitude-scale differences in [B] among different sample types: river samples < cold spring water < < brine lakes. [B] values vary from 0.73 to ~ 1113 mg/L. Similar to [B], the δ11B values of the samples exhibit magnitude-scale variations as [B], ranging from − 7.35‰ to + 7.66‰. There are also magnitude-scale differences in δ11B among different sample types. The δ11B values of cold spring water are relatively low, and the values range from − 1.26‰ to -7.75‰. However, the river water samples and saline lakes have higher values, from 0.38‰ to 4.62‰, and the δ11B values of river water samples are basically in the distribution range of those of Bangor Co Lake. This indicates that the sources of boron in Bangor Co Lake are mainly the recharge water with higher δ11B values and spring water with lower δ11B values, and the boron sources and the uneven mixing of lake water are two reasons that account for the large change in the δ11B value of Bangor Co Lake.

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10.
Pollen diagrams from Joe and Niliq Lakes date to ca. 28,000 and 14,000 yr B.P., respectively. Mesic shurb tundra grew near Joe Lake ca. 28,000 to 26,000 yr B.P. with local Populus populations prior to ca. 27,000 yr B.P. Shrub communities decreased as climate changed with the onset of Itkillik II glaciation (25,000 to 11,500 yr B.P.), and graminoid-dominated tundra characterized vegetation ca. 18,500 to 13,500 yr B.P. Herb tundra was replaced by shrub Betula tundra near both sites ca. 13,500 yr B.P. with local expansion of Populus ca. 11,000 to 10,000 yr B.P. and Alnus ca. 9000 yr B.P. Mixed Picea glauca/P. mariana woodland was established near Joe Lake ca. 6000 yr B.P. These pollen records when combined with others from northern Alaska and northwestern Canada indicate (1) mesic tundra was more common in northwestern Alaska than in northeastern Alaska or northwestern Canada during the Duvanny Yar glacial interval (25,000 to 14,000 yr B.P.); (2) with deglaciation, shrub Betula expanded rapidly in northwestern Alaska but slowly in areas farther east; (3) an early postglacial thermal maximum occurred in northwestern Alaska but had only limited effect on vegetation; and (4) pollen patterns in northern Alaska and northwestern Canada suggest regional differences in late Quaternary climates.  相似文献   

11.
(Fe, Mn)S and (Fe, Mg)S solid solutions are examined to study and compare the properties of Fe2+ in two different B1-structured hosts, and also to study the relative stability of the B1 (NaCl) and B8 (NiAs) structures at high pressure. The Mössbauer spectra of (Fe, Mn)S and (Fe, Mg)S B1 solid solutions are quadrupole doublets at 298 K with parameters which vary smoothly with Fe2+ concentration. At 4.2 K the Mössbauer spectra of (Fe, Mn)S and Fe-rich (Fe, Mg)S B1 solid solutions are magnetically split into eight lines, but the spectra of Mg-rich (Fe, Mg)S solid solutions are quadrupole doublets. The line widths of the magnetic spectra are broad, consistent with a multiaxial spin arrangement. Some properties of the hypothetical phase FeS(B1) are calculated from the solid solution data; the phase is inferred to be relatively ionic compared to FeS(B8) and has a molar volume that is 7.2 percent larger than the B8 phase at 298 K. The large inferred volume difference between FeS(B1) and FeS(B8) should cause exsolution of a B8-structured phase from (Fe, Mn)S and (Fe, Mg)S B1 solid solutions at high pressure. This behaviour is confirmed experimentally at high pressure using X-ray diffraction and Mössbauer spectroscopy, and the results are correlated with thermodynamic calculations of the phase boundaries based on estimates of the volume and free energy differences between the B1 and B8 phases of FeS derived from atmospheric pressure data. The absence of an increase in solubility of Mg and Mn in the B8 phase with pressure suggests that any polymorphism in MnS and MgS at high pressure is unlikely to involve the B8 phase. Shock wave data for MgO and Fe0.94O reported in the literature suggest similar behaviour in the system FeO-MgO at high pressure, namely exsolution of essentially pure FeO(hpp) from (Fe, Mg)O B1 solid solutions.  相似文献   

12.
Whole-rock chemical composition and 11B/10B isotope ratios in tourmaline was investigated to study the geochemical recycling of boron during the evolution of the Andean basement from the Palaeozoic to Mesozoic. In the basement (Cambrian to Ordovician high-grade paragneisses, migmatites and orthogneisses, the Eocambrian Puncoviscana Formation, and Paleozoic-Mesozoic granitoid igneous rocks) whole-rock B contents are generally below 100 ppm, but B contents of ˜1 wt% are found in cogenetic aplite and pegmatite dikes and in tourmaline–quartz rocks. In the metasedimentary rocks, no systematic variation in B content because of metamorphic grade and no correlation of B with other incompatible elements are apparent. Tourmalines from the high-grade metamorphic basement yield δ11B values ranging from −11.2 to −6.8‰ and isotope fractionation during migmatisation was small. Metamorphic tourmalines from the Puncoviscana Formation have δ11B values between −6.3 and −5.8‰. The calculated (corrected for fractionation) δ11B values of −6 to −2‰ for the sedimentary protolith of the metamorphic basement indicate a continental B source with subordinate marine input. Tourmalines from Palaeozoic and Mesozoic granitoids display an identical range of δ11B values from −12 to −5.3‰ and indicate a similarly homogeneous B source throughout time. Tourmalines from pegmatites and tourmaline–quartz rocks record the average δ11B values of the parental granitic magma. We assume that B in the Palaeozoic and Mesozoic granitoids is derived from the local metamorphic basement supporting the hypothesis that recycling of the lower Palaeozoic crust is the dominant process in granitic magma formation from Palaeozoic to Mesozoic. Received: 15 December 1999 / Accepted: 11 July 2000  相似文献   

13.
In this study, nineteen brine samples from the Qarhan Salt Lake (QSL) in western China were collected and analyzed for boron (B) and chlorine (Cl) concentrations, total dissolved solids (TDS), pH values and stable B isotopic compositions. The B concentrations and δ11B values of brines in the QSL range from 51.6 mg/L to 138.4 mg/L, and from +9.32‰ to +13.08‰, respectively. By comparison of B concentrations and TDS of brines in QSL with evaporation paths of brackish water, we found that B enrichment of brines primarily results from strong evaporation and concentration of Qarhan lake water. Combining with comparisons of B concentrations, TDS, pH values and δ11B values of brines, previously elemental ratios (K/Cl, Mg/Cl, Ca/Cl, B/Cl) and δ11B values of halite from a sediment core (ISL1A), we observe good correlations between B concentrations and TDS, TDS and pH values, pH and δ11B values of brines, which demonstrate that higher B concentrations and more positive δ11B values of halite indicate higher salinity of the Qarhan paleolake water as well as drier paleoclimatic conditions. Based on this interpretation of the δ11B values of halite in core ISL1A, higher salinity of the Qarhan paleolake occurred during two intervals, around 46–34 ka and 26–9 ka, which are almost coincident with the upper and lower halite-dominated salt layers in core ISL1A, drier climate phases documented from the δ18O record of carbonate in core ISL1A and the paleomoisture record in monsoonal central Asia, and a higher solar insolation at 30°N. These results demonstrate that the δ11B values of halite in the arid Qaidam Basin could be regarded as a new proxy for reconstructing the salinity record of paleolake water as well as paleoclimate conditions.  相似文献   

14.
The reported measurements for the stable isotopes of B (11B and 10B) in natural materials are compiled, critically reviewed and evaluated. The selected values along with a discussion of the error, indicate the potential exists for using B isotopes in interpreting geochemical environments. The isotopic values for δ11B range from -31%0 for terrestrial rocks to +40%0 for sea water, relative to NBS SRM-951 which has a reported 11B/10B ratio of 4.04362 ± 0.00137 (2σ). Furtherm the isotope ratios generally form a narrow cluster of values for specific rock types. In some instances the reported δ11B may be shifted substantially from the mean of “unaltered” rock as a result of weathering or reaction such as the progressive enrichment of δ11B in marine sediments over time due to reaction with sea water.An application of widespread interest is the use of B isotopes in environmental studies. Boron is a contaminant derived from numerous sources such as municipal and industrial waste. The δ11B in these wastes or processed waters is often significantly different from the δ11B of the local ground-water, which will likely reflect the δ11B values of the nearby rocks. This modification by contaminated water can be >20%0 different from the δ11B of the unaffected water, providing a useful tool in delineating the source of contamination and the direction of migration.  相似文献   

15.
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16.
《Applied Geochemistry》2006,21(4):643-655
The groundwater B concentration in the alluvial aquifer of the upper Cecina River basin in Tuscany, Italy, often exceeds the limit of 1 mg L−1 set by the European Union for drinking water. On the basis of hydrogeological and geochemical observations, the main source of the B contamination of groundwater has been attributed to past releases into streams of exhausted, B-rich geothermal waters and/or mud derived from boric acid manufacturing in Larderello. The releases were discontinued 25–30 years ago.This study confirms that the B dissolved in groundwater is anthropogenic. In fact, the δ11B values of groundwater B match the range −12.2‰ to −13.3‰ of the Turkish B mineral (colemanite) processed in boric acid manufacturing, in the course of which no significant isotopic effects have been observed. This isotopic tracing of the Cecina alluvial aquifer occurs just below the confluence of the Possera Creek, which carries the B releases from Larderello. Strontium isotope ratios support this conclusion.At about 18 km from the Possera Creek confluence, the groundwater δ11B drops to much more negative values (−22‰ to −27‰), which are believed to be produced by adsorption–desorption interactions between dissolved B and the aquifer matrix. The δ11B of B fixed in well bottom sediments shows a similar variation. At present, desorption is prevailing over adsorption because the releases of B-rich water have ceased. A theoretical model is suggested to explain the isotopic trends observed.Thus, B isotopes appear to be a powerful tool for identifying the origin of B contamination in natural waters, although isotopic effects associated with adsorption–desorption processes may complicate the picture, to some extent.  相似文献   

17.
Boron is an important micronutrient for plants but is toxic at high pore solution concentrations. Its mobility and migration in many geochemical environments is often controlled by reactions with mineral surfaces, and thus its speciation on mineral surfaces has been extensively investigated. Most previous studies have used IR spectroscopy to characterize the surface B-environments. We present here the first 11B MAS NMR study of surface sorbed boron on minerals. The results demonstrate the capability of this method to effectively probe the local structure of the sorption sites at total B-concentrations in the samples as small as 0.03 wt% and to provide insight into the mechanisms of sorption. Signal is readily resolved for both trigonal (B(3)) and tetrahedral (B(4)) boron exchanged onto boehmite, silica gel and illite, and the resonances are readily assigned on the basis of chemical shift and quadrupole coupling constant. Boron surface densities on illite are approximately order of magnitude greater than on silica gel or boehmite. For boehmite, both B(3) and B(4) occur dominantly as inner-sphere complexes formed by ligand exchange reaction with surface aluminol sites. The B(3)/[B(3) + B(4)] ratio of approximately 0.87 does not vary significantly with pH from 3 to 11, with solution B-concentration, or with washing. The occurrence of B(3) and B(4) as inner-sphere complexes is in agreement with previous suggestions from IR studies of B-sorption on iron hydroxide, allophone, kaolinite, and hydrous ferric oxide. For silica gel, B(3) and B(4) occur principally as outer-sphere complexes or as residual precipitate from un-removed solution. The B(3)/B(4) ratio decreases with increasing pH paralleling the speciation in solution, but the relative abundance of B(4) is greater than in solution. A small fraction of the B(4) occurs as inner-sphere complexes with B(4)-O-Si linkages formed by ligand exchange reaction with silanol sites. For illite, surface boron occurs as outer-sphere B(3) and B(4), as for silica gel, and as inner-sphere B(3) and B(4), as for boehmite. Outer-sphere B(3) and B(4) are dominant at pH 3 and 5, whereas inner-sphere B(3) and B(4) are dominant at pH 9 and 11. The inner-sphere complexes probably form dominantly by ligand exchange reactions involving sites on the broken edges of illite layers.  相似文献   

18.
The Tibetan plateau is characterized by intense hydrothermal activity and abnormal enrichment of trace elements in geothermal waters. Hydrochemistry and B isotope samples from geothermal waters in Tibet were systematically measured to describe the fractionation mechanisms and provide constraints on potential B reservoirs. B concentrations range from 0.35 to 171.90 mg/L, and isotopic values vary between −16.57 ‰ and +0.52 ‰. Geothermal fields along the Indus-Yarlung Zangbo suture zone and N–S rifts are observed with high B concentrations and temperatures. The similar hydrochemical compositions of high-B geothermal waters with magmatic fluid and consistent modeling of B isotopic compositions with present δ11B values imply that the B in high-B geothermal waters is mainly contributed by magmatic sources, probably through magma degassing. In contrast, geothermal fields in other regions of the Lhasa block have relatively low B concentrations and temperatures. After considering the small fractionation factor and representative indicators of Na/Ca, Cl/HCO3, Na + K and Si, the conformity between modeling results and the isotopic compositions of host rocks suggests that the B in low-temperature geothermal fields is mainly sourced from host rocks. According to simulated results, the B in some shallow geothermal waters not only originated from mixing of cold groundwater with deep thermal waters, but it was also contributed by equilibration with marine sedimentary rocks with an estimated proportion of 10%. It was anticipated that this study would provide useful insight into the sources and fractionation of B as well as further understanding of the relationships between B-rich salt lakes and geothermal activities in the Tibetan plateau.  相似文献   

19.
Pollen records from two sites in western Oregon provide information on late-glacial variations in vegetation and climate and on the extent and character of Younger Dryas cooling in the Pacific Northwest. A subalpine forest was present at Little Lake, central Coast Range, between 15,700 and 14,850 cal yr B.P. A warm period between 14,850 and 14,500 cal yr B.P. is suggested by an increase inPseudotsugapollen and charcoal. The recurrence of subalpine forest at 14,500 cal yr B.P. implies a return to cool conditions. Another warming trend is evidenced by the reestablishment ofPseudotsugaforest at 14,250 cal yr B.P. Increased haploxylonPinuspollen between 12,400 and 11,000 cal yr B.P. indicates cooler winters than before. After 11,000 cal yr B.P. warm dry conditions are implied by the expansion ofPseudotsuga.A subalpine parkland occupied Gordon Lake, western Cascade Range, until 14,500 cal yr B.P., when it was replaced during a warming trend by a montane forest. A rise inPinuspollen from 12,800 to 11,000 cal yr B.P. suggests increased summer aridity.Pseudotsugadominated the vegetation after 11,000 cal yr B.P. Other records from the Pacific Northwest show an expansion ofPinusfrom ca. 13,000 to 11,000 cal yr B.P. This expansion may be a response either to submillennial climate changes of Younger Dryas age or to millennial-scale climatic variations.  相似文献   

20.
《Applied Geochemistry》2001,16(7-8):821-834
The geological evolution of B in two UK sandstone aquifers is followed from precipitation chemistry through to groundwaters in both the unconfined and confined zones. Measurements have been made of major element geochemistry, B concentrations and B isotopic ratios. The isotopic measurements were carried out using ICP/MS following a simple preconcentration step. Isotopic measurements of rainfall show a bimodal distribution and it is suggested that enriched signatures are characteristic of Atlantic air over Britain and depleted signatures representative of continental air. In the marine Lower Greensand aquifer dissolution of glauconite results in the mobilisation of B and a correlation with SO4 suggests that this dissolution is related to the oxidation of pyrite which appears to be the SO4-forming reaction in the aquifer. In the non-marine Hastings beds isotopic ratios and a correlation with HCO3 suggest that B is associated with the dissolution of ferroan carbonates. In both aquifers the geochemical evolution of B is complex and more information is needed on the behaviour of B isotopes during evapotranspiration and groundwater recharge.  相似文献   

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