海洋生物碳酸盐δ11B-pH技术影响因素

肖军, 肖应凯, 刘丛强, 贺茂勇. 海洋生物碳酸盐δ11B-pH技术影响因素[J]. 海洋地质与第四纪地质, 2010, 30(4): 215-222. doi: 10.3724/SP.J.1140.2010.04215
引用本文: 肖军, 肖应凯, 刘丛强, 贺茂勇. 海洋生物碳酸盐δ11B-pH技术影响因素[J]. 海洋地质与第四纪地质, 2010, 30(4): 215-222. doi: 10.3724/SP.J.1140.2010.04215
XIAO Jun, XIAO Yingkai, LIU Congqiang, HE Maoyong. STUDY OF INFLUENCE FACTORS ON δ11B-PH TECHNIQUE FOR MARINE BIO-CARBONATE DEPOSITS[J]. Marine Geology & Quaternary Geology, 2010, 30(4): 215-222. doi: 10.3724/SP.J.1140.2010.04215
Citation: XIAO Jun, XIAO Yingkai, LIU Congqiang, HE Maoyong. STUDY OF INFLUENCE FACTORS ON δ11B-PH TECHNIQUE FOR MARINE BIO-CARBONATE DEPOSITS[J]. Marine Geology & Quaternary Geology, 2010, 30(4): 215-222. doi: 10.3724/SP.J.1140.2010.04215

海洋生物碳酸盐δ11B-pH技术影响因素

  • 基金项目:

    中国科学院地球环境研究所创新基金(O951071293)

    国家自然科学基金项目(40573013)

详细信息
    作者简介: 肖军(1980-),男,助理研究员,从事同位素地球化学研究,E-mail:xiaojun@ieecas.cn
  • 中图分类号: P597

STUDY OF INFLUENCE FACTORS ON δ11B-PH TECHNIQUE FOR MARINE BIO-CARBONATE DEPOSITS

  • 20世纪90年代以来,利用海洋生物碳酸盐的硼同位素组成重建古海水pH的δ11B-pH技术已成为国际同位素地球化学研究的热点。虽然该技术取得了很多的研究成果,但由于理论上的不完善,使该技术中存在一些尚未解决的问题,限制了该技术的近一步应用。综合近些年来的研究成果,对δ11B-pH技术中的不确定因素:海水B (OH)3的电离常数pKa、海水的δ11Bsw值、海水中B (OH)4-的δ11B值和海水B (OH)4-与B (OH)3间的分馏系数α进行了详细研究,提出了该技术今后研究的方向,为更好地利用海洋生物碳酸盐的硼同位素组成研究古海洋环境提供参考。
  • 加载中
  • [1]

    Mcmullen C C, Cragg C B, Thode H G. Absolute ratio of 11B-10B in searles lake borax[J]. Geochim Cosmochim Acta, 1961, 23:147-149.

    [2]

    Ishikawa T, Nakamura E. Boron isotope systematic of marine sediments[J]. Earth Planet. Sci. Lett., 1993, 117:567-580.

    [3]

    Hemming N G,Hanson G N. Boron isotopic composition and concentration in modern marine carbonates[J]. Geochim et Cosmochim Acta, 1992, 56:537-543.

    [4]

    Taylor S R,Mclennan S M. The Continental Crust:Its Composition and Evolution[M]. Blackwell scientific publication,1985.

    [5]

    Spivack A J, You C F, Smith J. Foraminiferal boron isotopic ratios as a proxy for surface ocean pH over the past 21 Myr[J]. Nature, 1993, 363:149-151.

    [6]

    Gaillardet J, Allègre C J. Boron isotopic compositions of co-ral:Seawater or diagenesis record?[J].Earth Plan. Sci. Lett., 1995, 136:665-676.

    [7]

    Sanyal A, Hemming N G, Hanson G N, et al. Evidence for a high pH in the glacial ocean from boron isotopes in foramini-fera[J]. Nature, 1995, 373:234-236.

    [8]

    Sanyal A, Hemming N G, Broecker W S, et al.Changes in pH in the eastern equatorial Pacific across stage 5-6 boundary based on boron isotopes in foraminifera[J]. Global Biogeochem Cycles, 1997, 11:125-133.

    [9]

    Palmer M R, Pearson P N, Cobb S J. Reconstructing past ocean pH-depth profiles[J]. Science, 1998, 282:1468-1471.

    [10]

    Pearson P N, Palmer M R. Middle Eocene seawater pH and atmospheric carbon dioxide concentration[J]. Science, 1999, 284:1824-1826.

    [11]

    Pearson P N, Palmer M R. Atmospheric carbon dioxide concentrations over the past 60 million years[J]. Nature, 2000, 406:695-699.

    [12]

    Lécuyer C, Grandjean P, Reynard B, et al.11B/10B analysis of geological materials by ICP-MS Plasma 54:Application to the boron fractionation between brachiopod calcite and seawater[J]. Chem. Geol., 2002, 186:45-55.

    [13]

    Spivack A J, Edmond J M. Boron isotope exchange between seawater and the oceanic crust[J]. Geochim. Cosmochim. Acta, 1987, 51:1033-1043.

    [14]

    Vengosh A, Vengosh A, Starinsky A, et al. Boron isotope geochemistry:as a tracer for the evolution of brine and associated hot springs from the Dead Sea Israel[J]. Geochim Cosomchim Acta, 1991(55):1689-1695.

    [15]

    Buch K. On boric acid in the sea and its influence on the carbonic acid equilibrium[J]. Journal du Conseil, Conseil Permanent International pour l'Exploration de la Mer, 1933, 8:309-325.

    [16]

    Lyman J. Buffer mechanism of seawater[D]. University of California, Los Angeles, USA.1956.

    [17]

    Hasson I. A new set of acidity constants for carbonic acid and boric in seawater[J]. Deep-Sea Research, 1973b, 20,461-478.

    [18]

    Dickson A G. Thermodynamics of dissociation of boric acid in synthetic seawater from 273.15 to 318.15 K[J]. Deep-Sea Res,1990, 37(5):755-766.

    [19]

    Richard E, Zeebe, Abhijit Sanyal, Joseph D et al. A theoretical study of the kinetics of the boric acid borate equilibrium in seawater[J]. Marine Chemistry, 2001, 73, 113-124.

    [20]

    Culberson C,Pytkowicz R M. Effect of pressure on carbonic acid, boric acid and the pH in seawater. Limnol[J]. Oceanogr, 1968, 13, 403-417.

    [21]

    Hershey J P, Fernande Z M, Milne P J, et al. The ionization of boric acid in NaCl, Na-Ca-Cl, and Na-Mg-Cl solutions at 25℃[J]. Geochim. Cosmochim. Acta, 1986, 50:143-148.

    [22]

    Roy R N, Roy L N, Vogel K M, et a1. Thermodynamics of the dissociation of boric acid in seawater[J]. Mar. Chem., 1993, 44:243-248.

    [23]

    Lemarchand D, Gaillardet J, Lewin E, et al. The influence of rivers on marine boron isotopes and implications for reconstructing past ocean pH[J]. Nature, 2000, 408:951-954.

    [24]

    Lemarchand D, Gaillardet J, Lewin E, et al.Boron isotope systematics in large rivers:implications for the marine boron budget and paleo-pH reconstruction over the Cenozoic[J]. Chem. Geol., 2002, 190:123-140.

    [25]

    Rose E R, Chaussidon M, FranceLanord C. Fractionation of boron isotopes during erosion processes:The example of Himalayan Rivers[J].Geochim Cosmochim Acta, 2000, 64(3):397-408.

    [26]

    Muto S. Geochemical studies of boron Ⅱ, The source of boron in rain water[J]. J. Chem. Soc. Japan, 1956:1770-1773.

    [27]

    Spivack A J, Palmer M R, Edmond J M. The sedimentary cycle of the boron isotopes[J]. Geochim. Cosmochim. Acta, 1987, 51:1939-1949.

    [28]

    Kopfa, Deyhle A. Back to the roots:Boron geochemistry of mud volcanoes and its implications for mobilization depth and global B cycling[J]. Chemical Geology, 2002, 192(3/4):195-210.

    [29]

    Schwarcz H P, Agyei K, McMullen C C. Boron isotopic fractionation during clay adsorption from seawater[J]. Earth Planet. Sci. Lett, 1969, 6:1-5.

    [30]

    Spivack A J, Edmond J M. Boron isotope exchange between seawater and the oceanic crust[J]. Geochim. Cosmochim. Acta, 1987, 51:1033-1043.

    [31]

    Smith H J, Spivack A J, Staudigel H, et al. The boron isotopic composition of altered oceanic crust[J]. Chem. Geol., 1995, 126:119-135.

    [32]

    Gast J A, Thompson T G. Evaporation of boric acid from seawater[J]. Tellus, 1959, 6:344-347.

    [33]

    Nishimura M,Tanaka K. Seawater may not be a source of boron in the atmosphere[J].J. Geoph. Res., 1972, 77:5239-5242.

    [34]

    Savenko V S. Is boric acid evaporation from sea water the major boron source in the atmosphere?[J]. Oceanology, 1977, I7:290-292.

    [35]

    Fogg T R, Duee R A. Boron in the troposphere:Distribution and fluxes[J]. J. Geoph. Res., 1985, 90:3781-3796.

    [36]

    Joachimski M, Simon L, Geldem R. Boron isotope geochemistry of Paleozoic brachiopod calcite:Implications for a secular change in the boron isotope geochemistry of seawater over the Phanerozoic[J]. Geochimica et Cosmochimica Acta, 2005, 69(16):4035-4044.

    [37]

    Simon L, Lcuyer C, Marchal, et al. Modeling the geochemical cycle of boron:Implications for the long-term δ11B evolution of seawater and oceanic crust[J]. Chemical Geology, 2006, 225(1/2):61-67.

    [38]

    Hemming N G, Reeder R J, Hanson G N. Mineral-fluid partitioning and isotopic fractionation of boron in synthetic cal-cium carbonate[J]. Geochim. Cosmochim. Acta, 1995, 59:371-379.

    [39]

    Sanyal A, Nugent M, Reeder R J, et al. Seawater pH control on the boron isotopic composition of calcite:Evidence from inorganic calcite precipitation experiments[J]. Geochim. Cosmochim. Acta, 2000, 64:1551-1555.

    [40]

    肖应凯, 李世珍, 魏海珍, 等. 从海/咸水中沉积碳酸钙时异常的硼同位素分馏[J]. 中国科学B辑, 2006, 36(3):263-272.

    [XIAO Yingkai, LI Shizhen, WEI Haizhen, et al.An unusual isotopic fractionation of boron in synthetic calcium carbonate precipitated from seawater and saline water[J]. Science in China Series B:Chemistry 2006,49(5):454-465.]

    [41]

    XIAO Jun, XIAO Yingkai, LIU Congqiang, et al. Boron isotope fractionation during incorporation of boron into Mg(OH)2[J]. Chinese Science Bulletin, 2009, 54(1):3090-3100.

    [42]

    Nothdurft L D, Webb G E, Buster N A, et al. Brucite microbialites in living coral skeletons:Indicators of extreme microenvironments in shallow-marine settings[J]. Geology, 2005, 33:169-172.

    [43]

    Sanyal A, Hemming N G, Broecker W S. Oceanic pH control on the boron isotopic composition of foraminifera:Evidence from culture experiments[J]. Paleoceanography, 1996, 11(5):513-517.

    [44]

    Hönisch B,Hemming N G, Grottoli A G, et al. Assessing scleratinian corals as recorders for paleo-pH:Empirical calibration and vital effects[J]. Geochim. Cosmochim. Acta, 2004, 68(18):3675-3685.

    [45]

    Palmer M R, Spivack A J, Edmond J M. Temperature and pH controls over isotopic fractionation during absorption of boron marine clay[J]. Geochim. Cosmochim. Acta, 1987, 51:2319-2323.

    [46]

    肖应凯,李华玲,刘卫国,等.无机碳酸盐沉积的硼同位-B(OH)3掺入碳酸盐的证据[J].中国科学D辑,2008,38(10):1309-1317.

    [XIAO Yingkai, LI Hualing,LIU Weiguo, et al. Boron isotopic fractionation in laboratory inorganic carbonate precipitation:Evidence for the incorporation of B(OH)3 into carbonate[J]. Science in China Series D:Earth Sciences,2008,51(12):1776-1785.]

    [47]

    李华玲,肖应凯,魏海珍,等.三亚活体珊瑚的微量元素与硼同位素组成的进行初步研究[J].盐湖研究,2006,14(2):35-41.

    [LI Hualing, XIAO Yingkai,WEI Haizhen, et al.Preliminary study for trace element and isotopic compositions of boron in growing corals from Sanya Bay,China[J].Journal of Salt Lake Research,2006,14(2):35-41.]

    [48]

    Pagani M, Lamarchand D, Spivack A,et al. A critical evalua-tion of the boron isotope-pH proxy:The accuracy of ancient ocean pH estimates[J]. Geochim Cosmochim Acta, 2005, 69:953-961.

    [49]

    Kakihana H, Kotaka M, Satoh S, et al. Fundamental studies on the ion-exchange separation of boron isotopes[J].Bulletin of the Chemical Society of Japan, 1977, 50(1):158-163.

    [50]

    Richard E, Zeebe. Stable boron isotope fractionation between dissolved B(OH)3 and B(OH)4-[J]. Geochim. Cosmochim. Acta, 2005, 69(11):2753-2766.

    [51]

    Byrne R H, Yao W, Klochko, K, et al. Experimental evaluation of the isotopic exchange equilibrium 10B(OH)3+11B(OH)4-=11B(OH)3 +10B(OH)4- in aqueous solution[J]. Deep-Sea Research, 2006, 153:684-688.

    [52]

    Oi T. Ab initio orbital calculations of reduced partition function ratios of polyboric acids and borate anions. Z[J]. Naturforsch., 2000, 55a:623-628.

    [53]

    Liu Y, Tossell J A. Ab initio molecular orbital calculations for boron isotope fractionations on borinc acids and borates[J]. Geochim. Cosmochim. Acta., 2005, 69:3995-4006.

    [54]

    Klochko K, Kaufman A J, Yao W, et al. Experimental measurement of boron isotope fractionation in seawater[J]. Earth Plan. Sci. Lett., 2006, 248:276-285.

    [55]

    刘耘. 稳定同位素分馏的量子化学计算研究-以硼和铁同位素为例[J].矿物岩石地球化学通报,2006,25(增刊):124-126.[LIU Yun. Quantum chemistry research of stable isotopic fractionation-boron and iron isotop[J].Bulletin of Mineralogy,Petrology and Geochemistry. 2006

    , 25(sup.):124-126.]

    [56]

    Hönisch B, Hemming N G, Loose B.Comment on "A critical evaluation of the boron isotope-pH proxy:The accuracy of ancient ocean pH estimates" by Pagani M, Lemarchand D, Spivack A andGaillardet J[J]. Geochim. Cosmochim. Acta, 2007, 71:1636-1641.

    [57]

    Pagani M, Spivack A J. Response to the Comment by B. Hönisch, N.G. Hemming, B. Loose on ‘A critical evaluation of the boron isotope-pH proxy:The accuracy of ancient ocean pH estimates’[J]. Geochim. Cosmochim. Acta, 2007, 71:1642.

  • 加载中
计量
  • 文章访问数:  1449
  • PDF下载数:  1
  • 施引文献:  0
出版历程
收稿日期:  2009-11-09
修回日期:  2010-02-11

目录