By using the multi-tube sediment samples collected from NB01 station in the Bering Sea during the period of the fourth Chinese Arctic research expedition in 2010,as well as the dating technique of radioisotope ^(210)P...By using the multi-tube sediment samples collected from NB01 station in the Bering Sea during the period of the fourth Chinese Arctic research expedition in 2010,as well as the dating technique of radioisotope ^(210)Pb in sedimentary strata,based on the exponential decay trend of ^(210)Pb exwith the column sample depth,relative stable modern sedimentary environment in the investigation area was reflected. The results show that the deposition rate of modern marine sediment S was 0. 27 cm/a,and correlation coefficient R was 0. 96( n = 17),while time span was 107 a(1903-2010). Meanwhile,carbon,nitrogen and isotopes were used to trace the sources of materials in the Bering Sea. It is found that the content of organic carbon and nitrogen in the column samples from NB01 station in the Bering Sea was 1. 18%-1. 80% and 0. 16%-0. 28% respectively,and C/N ratio ranged from 5. 13 to 8. 31. Total organic carbon( TOC) and total organic nitrogen( TON) were preserved well in sedimentary strata and had good consistency,showing that sources of organic matter were consistent. Moreover,their changes positively correlated with^(210)Pb. Organic carbon isotope( δ13 C) ranged from-22. 45‰ to-21. 82‰,and its changing trend was similar to that of C/N ratio; organic nitrogen isotope(δ15 N) varied from 7. 53‰ to 8. 54‰,indicating that organic matter was mainly from remaining marine organisms after being decomposed,into which a certain quantity of terrigenous materials were mixed. In the 100 years,the overall trend of terrigenous materials became increasingly obvious,showing that the input and burial of organic carbon from seas and land in the Bering Sea were changing. According to the burial rate of surface sediment and content of organic carbon,the apparent burial flux of sedimentary organic carbon in the column sample from NB01 station in the Bering Sea was estimated,about 1 450 mmol C/( m^2·a). It is suggested that the high burial flux of sedimentary organic carbon in the regions was mainly related to the high primary productivity of the water body,the high output efficiency of organic carbon in the photic zone,favorable preservation and metabolic mechanism of organic matter,and high deposition rate.展开更多
大气^(210)Po、^(210)Bi和^(210)Pb的沉降通量是海洋中核素示踪颗粒物动力学过程(颗粒有机碳输出、颗粒物输运)的基础参数,为揭示我国近海地区^(210)Po、^(210)Bi和^(210)Pb活度浓度的时空变化规律并估算其沉降入海通量,本文于2016年9...大气^(210)Po、^(210)Bi和^(210)Pb的沉降通量是海洋中核素示踪颗粒物动力学过程(颗粒有机碳输出、颗粒物输运)的基础参数,为揭示我国近海地区^(210)Po、^(210)Bi和^(210)Pb活度浓度的时空变化规律并估算其沉降入海通量,本文于2016年9月至翌年2月和2021年9-11月分别对上海及厦门地区近地表大气气溶胶中^(210)Po、^(210)Pb和^(210)Bi的活度浓度进行了连续观测;基于^(210)Po-^(210)Pb活度比(^(210)Po/^(210)Pb)和^(210)Bi-^(210)Pb活度比(^(210)Bi/^(210)Pb)两种示踪法计算了气溶胶颗粒物的滞留时间,并利用一维简单气溶胶沉降速率模型估算了3种核素以大气沉降方式输入东海的通量。结果显示,2016年上海秋、冬两季^(210)Po、^(210)Bi、^(210)Pb 3种核素活度浓度的变化范围分别为0.11~1.27 m Bq/m^(3)、0.45~1.83 m Bq/m^(3)和1.12~6.10 m Bq/m^(3);2021年秋季厦门^(210)Po、^(210)Bi、^(210)Pb 3种核素活度浓度的变化范围分别为0.05~0.85 m Bq/m^(3)、0.83~2.52 m Bq/m^(3)和0.17~1.32 m Bq/m^(3),上海近地表气溶胶中3种核素的活度浓度秋季平均值比厦门地区高。利用^(210)Po/^(210)Pb和^(210)Bi/^(210)Pb计算得到上海和厦门近地面大气的气溶胶滞留时间存在显著差异,基于^(210)Po/^(210)Pb计算上海气溶胶滞留时间均值为(94±54)d,基于^(210)Bi/^(210)Pb计算上海气溶胶滞留时间均值为(6.4±4.8)d,造成这种差异的原因很可能是两种示踪法本身具有的系统性差异。本文基于一维简易气溶胶沉降速率模型估算了上海地区的^(210)Pb、^(210)Bi和^(210)Po的大气沉降入东海的通量,其在秋季期间的变化范围分别为0.1~26.35 Bq/(m^(2)·d)、0.04~7.91 Bq/(m^(2)·d)和0.01~5.49 Bq/(m^(2)·d)。基于模型估算的^(210)Po、^(210)Bi和^(210)Pb沉降通量与研究区域的实际观测值接近一致,表明利用一维简易气溶胶沉降速率模型间接估算法在替代观测站直测核素的沉降入海通量方面具有一定可行性。展开更多
基金Supported by National Natural Science Foundation of China(4127-6199)Chinese Projects for Investigations and Assessments of the Arctic and Antarctic(CHINARE 2012-2016 for 03-04 and 04-03)
文摘By using the multi-tube sediment samples collected from NB01 station in the Bering Sea during the period of the fourth Chinese Arctic research expedition in 2010,as well as the dating technique of radioisotope ^(210)Pb in sedimentary strata,based on the exponential decay trend of ^(210)Pb exwith the column sample depth,relative stable modern sedimentary environment in the investigation area was reflected. The results show that the deposition rate of modern marine sediment S was 0. 27 cm/a,and correlation coefficient R was 0. 96( n = 17),while time span was 107 a(1903-2010). Meanwhile,carbon,nitrogen and isotopes were used to trace the sources of materials in the Bering Sea. It is found that the content of organic carbon and nitrogen in the column samples from NB01 station in the Bering Sea was 1. 18%-1. 80% and 0. 16%-0. 28% respectively,and C/N ratio ranged from 5. 13 to 8. 31. Total organic carbon( TOC) and total organic nitrogen( TON) were preserved well in sedimentary strata and had good consistency,showing that sources of organic matter were consistent. Moreover,their changes positively correlated with^(210)Pb. Organic carbon isotope( δ13 C) ranged from-22. 45‰ to-21. 82‰,and its changing trend was similar to that of C/N ratio; organic nitrogen isotope(δ15 N) varied from 7. 53‰ to 8. 54‰,indicating that organic matter was mainly from remaining marine organisms after being decomposed,into which a certain quantity of terrigenous materials were mixed. In the 100 years,the overall trend of terrigenous materials became increasingly obvious,showing that the input and burial of organic carbon from seas and land in the Bering Sea were changing. According to the burial rate of surface sediment and content of organic carbon,the apparent burial flux of sedimentary organic carbon in the column sample from NB01 station in the Bering Sea was estimated,about 1 450 mmol C/( m^2·a). It is suggested that the high burial flux of sedimentary organic carbon in the regions was mainly related to the high primary productivity of the water body,the high output efficiency of organic carbon in the photic zone,favorable preservation and metabolic mechanism of organic matter,and high deposition rate.
文摘大气^(210)Po、^(210)Bi和^(210)Pb的沉降通量是海洋中核素示踪颗粒物动力学过程(颗粒有机碳输出、颗粒物输运)的基础参数,为揭示我国近海地区^(210)Po、^(210)Bi和^(210)Pb活度浓度的时空变化规律并估算其沉降入海通量,本文于2016年9月至翌年2月和2021年9-11月分别对上海及厦门地区近地表大气气溶胶中^(210)Po、^(210)Pb和^(210)Bi的活度浓度进行了连续观测;基于^(210)Po-^(210)Pb活度比(^(210)Po/^(210)Pb)和^(210)Bi-^(210)Pb活度比(^(210)Bi/^(210)Pb)两种示踪法计算了气溶胶颗粒物的滞留时间,并利用一维简单气溶胶沉降速率模型估算了3种核素以大气沉降方式输入东海的通量。结果显示,2016年上海秋、冬两季^(210)Po、^(210)Bi、^(210)Pb 3种核素活度浓度的变化范围分别为0.11~1.27 m Bq/m^(3)、0.45~1.83 m Bq/m^(3)和1.12~6.10 m Bq/m^(3);2021年秋季厦门^(210)Po、^(210)Bi、^(210)Pb 3种核素活度浓度的变化范围分别为0.05~0.85 m Bq/m^(3)、0.83~2.52 m Bq/m^(3)和0.17~1.32 m Bq/m^(3),上海近地表气溶胶中3种核素的活度浓度秋季平均值比厦门地区高。利用^(210)Po/^(210)Pb和^(210)Bi/^(210)Pb计算得到上海和厦门近地面大气的气溶胶滞留时间存在显著差异,基于^(210)Po/^(210)Pb计算上海气溶胶滞留时间均值为(94±54)d,基于^(210)Bi/^(210)Pb计算上海气溶胶滞留时间均值为(6.4±4.8)d,造成这种差异的原因很可能是两种示踪法本身具有的系统性差异。本文基于一维简易气溶胶沉降速率模型估算了上海地区的^(210)Pb、^(210)Bi和^(210)Po的大气沉降入东海的通量,其在秋季期间的变化范围分别为0.1~26.35 Bq/(m^(2)·d)、0.04~7.91 Bq/(m^(2)·d)和0.01~5.49 Bq/(m^(2)·d)。基于模型估算的^(210)Po、^(210)Bi和^(210)Pb沉降通量与研究区域的实际观测值接近一致,表明利用一维简易气溶胶沉降速率模型间接估算法在替代观测站直测核素的沉降入海通量方面具有一定可行性。
