Burial fluxes and source apportionment of carbon in culture areas of Sanggou Bay over the past 200 years     

LIU Sai  HUANG Jiansheng  YANG Qian  YANG Shu  YANG Guipeng  SUN Yao 《海洋学报(英文版)》2015,34(10):23-30

In this study,we assessed the burial fluxes and source appointment of different forms of carbon in core sediments collected from culture areas in the Sanggou Bay,and preliminarily analyzed the reasons for the greater proportion of inorganic carbon burial fluxes(BFTIC).The average content of total carbon(TC) in the Sanggou Bay was 2.14%.Total organic carbon(TOC) accounted for a small proportion in TC,more than 65% of which derived from terrigenous organic carbon(Ct),and while the proportion of marine-derived organic carbon(Ca) increased significantly since the beginning of large-scale aquaculture.Total inorganic carbon(TIC) accounted for 60%–75%of TC,an average of which was 60%,with a maximum up to 90% during flourishing periods(1880–1948) of small natural shellfish derived from seashells inorganic carbon(Shell-IC).The TC burial fluxes ranged from 31 g/(m2·a)to 895 g/(m2·a) with an average of 227 g/(m2·a),which was dominated by TIC(about 70%).Shell-IC was the main source of TIC and even TC.As the main food of natural shellfish,biogenic silica(BSi) negatively correlated with BFTIC through affecting shellfish breeding.BFTIC of Sta.S1,influenced greatly by the Yellow Sea Coastal Current,had a certain response to Pacific Decadal Oscillation(PDO) in some specific periods.  相似文献   

二甲基硫的海洋化学研究   总被引：2，自引：1，他引：1  

杨桂朋  戚佳琳 《中国海洋大学学报(自然科学版)》1999,(Z1)

二甲基硫（ＤＭＳ） 是海洋排放到大气中的最主要的生源硫化物。作者综述了ＤＭＳ在海洋中的分布特征、影响ＤＭＳ转化的因素、ＤＭＳ的海空扩散及其对环境的影响等。ＤＭＳ在海洋中存在很大程度的时空变化,这一变化不仅与海洋初级生产力水平有关,而且还与浮游植物的种类组成密切相关。微生物的降解、光化学的氧化以及海空扩散是ＤＭＳ在海洋中迁移变化的三个最重要的途径。ＤＭＳ的海－ 空扩散也存在较大的时空变化。ＤＭＳ的释放会对全球的气候变化和酸雨的形成产生重要的影响。本文同时就国内外的研究现状和今后的研究方向进行了分析和总结。  相似文献   

Chemical characterization and composition of dissolved organic matter in Jiaozhou Bay   总被引：1，自引：0，他引：1  

张艳萍  杨桂朋  陈岩 《中国海洋湖沼学报》2009,27(4):851-858

Biologically utilizable dissolved organic compounds, including dissolved organic carbon (DOC), dissolved carbohydrates (DCHO) and dissolved free amino acids (DFAA) were analyzed in filtered surface seawater samples collected at 19 stations in Jiaozhou Bay, China, on June 3, 2007. In these samples, concentrations of DOC, dissolved free carbohydrates (DFCHO), dissolved combined carbohydrates (DCCHO), total dissolved carbohydrates (TDCHO) and total dissolved free amino acids (TDFAA) ranged from 141.7 to 191.1 μmol C/L, 1.98 to 18.18 μmol C/L, 5.04 to 24.90 μmol C/L, 14.52 to 30.36 μmol C/L, and 1.83 to 11.89 μmol C/L, respectively. As a major component of the dissolved carbohydrates, the concentrations of DCCHO were about three times higher than those of DFCHO. Three major constituents of the DFAA were threonine (23.0±5.7 mol%), glutamic acid (16.6±3.2 mol%) and arginine (9.1±3.3 mol%). Based on the composition of DFAA, a molar C:N ratio of 3.60±0.75 in DFAA was derived, indicating longer carbon chains in the amino acids. DCCHO (8.1%) was the most abundant fraction of DOM in most samples, followed by DFCHO (4.8%) and TDFAA (2.7%). These DOM concentrations displayed a decreasing trend from the coast to the central region. Significant correlations were found between the DCCHO and DFCHO concentrations (r=-0.724, n=19, P<0.001) and the DCCHO and TDCHO concentrations (r=0.506, n=19, P=0.027).  相似文献   

Dissolved and Particulate Dimethylsulfoxide in the South China Sea During Winter     

Jie Yang  Guipeng Yang 《中国海洋大学学报(英文版)》2018,17(6):1343-1351

The distributions of particulate and dissolved dimethylsulfoxide(DMSOp, DMSOd) were studied for the first time in the surface water of the South China Sea(SCS) in January 2010. The concentrations of DMSOp ranged from 2.6 to 56.8 nmol L~(-1) with an average of 11.1 ± 2.2 nmol L~(-1), and those of DMSOd ranged from 11.8 to 335.1 nmol L~(-1) with an average of 50.0 ± 16.5 nmol L~(-1). DMSOd dominated over both dimethylsulfide(DMS) and dissolved dimethylsulfoniopropionate(DMSPd) by 1–3 orders of magnitude and represented the major dissolved dimethyl sulfur pool. In addition, DMSOp/chlorophyll-a ratios varied from 2.7 to 180.7 mmol g~(-1) with an average of 30.5 ± 9.6 mmol g~(-1). DMSOd concentrations displayed a significant negative relationship with sea surface temperature(SST) and sea surfaces salinity(SSS) in the whole study area. The distribution of DMSOd in the coastal waters was obviously influenced by the Pearl River discharge, with high concentrations appearing around the river mouth. In the offshore waters, a significant correlation was observed between the DMSOp and DMSOd concentrations, suggesting that DMSOd was mainly from the diffusion of intracellular DMSO rather than from the photochemical and biological oxidation of DMS.  相似文献   

Distributions and Relationships of CO_2,O_2,and Dimethylsulfide in the Changjiang(Yangtze) Estuary and Its Adjacent Waters in Summer     

WU Xi  TAN Tingting  LIU Chunying  LI Tie  LIU Xiaoshou  YANG Guipeng 《中国海洋大学学报(英文版)》2018,(2)

The distributions and relationships of O_2, CO_2, and dimethylsulfide (DMS) in the Changjiang (Yangtze) Estuary and its adjacent waters were investigated in June 2014. In surface water, mean O_2 saturation level, partial pressure of CO_2 (pCO_2), and DMS concentrations (and ranges) were 110% (89%–167%), 374μatm (91–640 μatm), and 8.53 nmol L~(-1) (1.10–27.50 nmol L~(-1)), respectively. The sea-to-air fluxes (and ranges) of DMS and CO_2 were 8.24 μmol m~(-2)d~(-1) (0.26–62.77 μmol m~(-2)d~(-1)), and -4.7 mmol m~(-2)d~(-1) (-110.8-31.7 mmol m~(-2)d~(-1)), respectively. Dissolved O_2 was oversaturated, DMS concentrations were relatively high, and this region served as a sink of atmospheric CO_2. The pCO_2 was significantly and negatively correlated with the O_2 saturation level, while the DMS concentration showed different positive relationships with the O_2 saturation level in different water masses. In vertical profiles, a hypoxic zone existed below 20 m at a longitude of 123?E. The stratification of temperature and salinity caused by the Taiwan Warm Current suppressed seawater exchange between upper and lower layers, resulting in the formation of a hypoxic zone. Oxidative de-composition of organic detritus carried by the Changjiang River Diluted Water (CRDW) consumed abundant O_2 and produced additional CO_2. The DMS concentrations decreased because of low phytoplankton biomass in the hypoxic zone. Strong correlations ap-peared between the O_2 saturation level, pCO_2 and DMS concentrations in vertical profiles. Our results strongly suggested that CRDW played an important role in the distributions and relationships of O_2, CO_2, and DMS.  相似文献   

Distributions and Relationships of CO<Subscript>2</Subscript>, O<Subscript>2</Subscript>, and Dimethylsulfide in the Changjiang (Yangtze) Estuary and Its Adjacent Waters in Summer     

Xi Wu  Tingting Tan  Chunying Liu  Tie Li  Xiaoshou Liu  Guipeng Yang 《中国海洋大学学报(英文版)》2018,17(2):320-334

The distributions and relationships of O₂, CO₂, and dimethylsulfide (DMS) in the Changjiang (Yangtze) Estuary and its adjacent waters were investigated in June 2014. In surface water, mean O₂ saturation level, partial pressure of CO₂ (pCO₂), and DMS concentrations (and ranges) were 110% (89%–167%), 374 μatm (91–640 μatm), and 8.53 nmol L^?1 (1.10–27.50 nmol L^?1), respectively. The sea-to-air fluxes (and ranges) of DMS and CO₂ were 8.24 μmol m^?2 d^?1 (0.26–62.77 μmol m^?2 d^?1), and ?4.7 mmol m^?2 d^?1 (?110.8-31.7 mmol m^?2 d^?1), respectively. Dissolved O₂ was oversaturated, DMS concentrations were relatively high, and this region served as a sink of atmospheric CO₂. The pCO₂ was significantly and negatively correlated with the O₂ saturation level, while the DMS concentration showed different positive relationships with the O₂ saturation level in different water masses. In vertical profiles, a hypoxic zone existed below 20 m at a longitude of 123°E. The stratification of temperature and salinity caused by the Taiwan Warm Current suppressed seawater exchange between upper and lower layers, resulting in the formation of a hypoxic zone. Oxidative decomposition of organic detritus carried by the Changjiang River Diluted Water (CRDW) consumed abundant O₂ and produced additional CO₂. The DMS concentrations decreased because of low phytoplankton biomass in the hypoxic zone. Strong correlations appeared between the O₂ saturation level, pCO₂ and DMS concentrations in vertical profiles. Our results strongly suggested that CRDW played an important role in the distributions and relationships of O₂, CO₂, and DMS.  相似文献   

巴丹吉林沙漠湖泊水化学空间分布特征   总被引：7，自引：2，他引：5  

陆莹  王乃昂  李贵鹏  李卓仑  董春雨  路俊伟 《湖泊科学》2010,22(5):774-782

通过对巴丹吉林沙漠腹地拐子湖-地质公园一线51个湖泊水,8个泉水,12个井水及1个雨水水样的水化学成分分析,初步探讨了沙漠湖泊水化学分布特征及其影响因素.结果表明由东南边缘至腹地湖泊总体上依次呈硫酸盐型-碳酸盐型-氯化物型分布.东南边缘以Na+、Cl-、SO24-为主的湖泊因矿化度分异,形成Ca2+、Mg2+含量不同的三种亚型,其中高矿化度的Na-Cl-(SO4)型湖泊在腹地湖泊群中也有出现,表现出地理上的不连续分布;边缘若干湖泊受局部地理环境的影响水离子多含Na+、Cl-、CO32-+HCO3-.综合分析表明湖泊水化学型的空间分异与区域气候差异和气候变化有关,湖水直接或间接地接受当地降水补给,但不排除外源地下水补给对其有一定贡献.通过对比不同时段部分沙漠湖泊水化学特征发现近十年以来腹地湖泊补给源或受气候干暖化影响使其水化学特性较边缘湖泊的变化大.  相似文献   

胶州湾海水中一氧化碳光致生成影响因素的研究     

陆小兰  张聪  杨桂朋  谭勇  任春艳 《海洋学报(英文版)》2012,31(4):77-83

海水中的一氧化碳(CO)主要由溶解有色有机物(CDOM)光降解产生,且CO的光致生成量受到环境因素的影响。采集了胶州湾及其河口表层水样,通过实验室模拟实验开展了不同的环境条件(辐射强度、光照时间、温度、pH和盐度)以及水体中CDOM的来源对CO光致生成的影响研究。结果表明胶州湾海水中CO的光致生成速率随辐射强度的增强、水温的升高和水体pH的增大而增大;随着光照时间的延长、水体盐度的增大而逐渐减小;不同来源的CDOM对水体中CO的光致生成速率产生了不同的影响。  相似文献   

Photochemical degradation of triadimefon in seawater     

Xiaochun Sun  Guipeng Yang  Xiaoyan Cao  Zhifeng Lin 《中国海洋大学学报(英文版)》2008,7(2):171-176

The photochemical degradation of triadimefon in seawater was investigated under different reaction conditions in this study. The results showed that triadimefon could be effectively degraded by the irradiation of a high-pressure mercury lamp and the photodegradation rotes were influenced by aquatic media, heavy metal ions and photosensitizers. The photochemical degradation of triadimefon followed the first-order reaction kinetic behavior, with the rate constants ranging from 0.0027 to 0.0128 min-1 under the studied conditions. The photolysis of triadimefon was slower in natural seawater than in distilled water or synthetic seawater. All the heavy metal ions studied in this paper had inhibition effects on the photolysis of triadimefon. Acetone, as a common photosensitizer, could accelerate the photolysis of triadimefon. Three photoproducts were identified by GC-MS analysis. Our study confirmed that photochemical degradation is an effective pathway to remove triadimefon in seawater.  相似文献   

Spatial distribution of dimethylsulfide and dimethylsulfoniopropionate in the Yellow Sea and Bohai Sea during summer   总被引：1，自引：0，他引：1  

杨剑  杨桂朋  张洪海  张升辉 《中国海洋湖沼学报》2015,33(4):1020-1038

Abstrac t The distributions of dimethylsulfide(DMS) and its precursor dimethylsulfoniopropionate(DMSP) in surface water of the Yellow Sea and the Bohai Sea were studied during June 2011. The mean concentrations and ranges of DMS, dissolved DMSP(DMSPd), and particulate DMSP(DMSPp) in surface waters were 6.85(1.60–12.36), 7.25(2.28–19.05) and 61.87(6.28–224.01) nmol/L, respectively. There were strong correlations between DMSPp and chlorophyll a in the Bohai Sea and the North Yellow Sea, respectively, and concentrations of DMS and DMSP were high, with a relatively high proportion of dinoflagellates, in the region of the South Yellow Sea Cold Water Mass. Results show that phytoplankton biomass and species composition were important factors that controlled the distribution of DMS and DMSP. Complex environmental factors, including nutrients, transparency, and terrestrial runoff, might also influence the variability in DMS and DMSP. Biological production and consumption rates of DMS in the Bohai Sea were higher than those in the Yellow Sea. DMS production rates were closely correlated with DMSPd concentrations. DMS and DMSP exhibited obvious diel variations, with high concentrations occurring in the late afternoon(16:00–19:00) and low concentrations occurring during the night, implying that the intensity of solar radiation had a significant influence on these variations. Size distributions of chlorophyll a and DMSPp were also investigated and large nanoplankton(5–20 μm), mainly diatoms, contributed significantly to chlorophyll a and DMSPp at most stations. The average sea-to-air flux of DMS in the study area was estimated to be 11.07 μmol/(m2 ·d) during the summer.  相似文献