黄河利津水文站不同粒径悬浮颗粒物中有机碳含量的研究

估算不同粒径TSS中POC的入海日通量,对黄河利津水文站悬浮颗粒物(total suspended solid,TSS)样品,采用基于stokes原理的沉降法分为Ⅴ级,对分级后的样品测其有机碳(particulate organic carbon,POC)含量和粒度组成。在此基础上,用多元线性回归法对数据进一步处理,准确得到样品中不同粒径TSS中POC的含量。研究表明,黄河口淡水端水体TSS,<8μm的粘土和极细粉砂、8~16μm的细粉砂中,POC的含量为0.600%和0.400%左右;16~32μm的中粉砂中,POC的含量不足0.200%;而32~63μm的粗粉砂和>63μm砂中POC含量仅为0.050%和0.004%左右,80%以上的POC主要集中在<16μm的TSS中,而<32μm的TSS承载了95%以上的POC。     

浮游植物生物量研究 Ⅰ.浮游植物生物量细胞体积转化法

在海洋生态动力学研究过程中,采用浮游植物细胞数量来估算浮游植物丰度可以说是不够精确的,因为不同种的浮游植物细胞大小差别很大,只有浮游植物的生物量才能正确反映海洋生态系中的能量分布．本文以拟合浮游植物细胞相似体积方法,基于胶州湾生态动力学研究所获资料,计算了87种中国近海常见浮游植物的细胞体积、鲜重、碳含量、氮含量．     

Deposition Rates of Terrestrial and Marine Organic Carbon in the Osaka Bay, Seto Inland Sea, Japan, Determined Using Carbon and Nitrogen Stable Isotope Ratios in the Sediment

Carbon and nitrogen stable isotope ratios (¹³C and ¹⁵N) of surface sediments were measured within Osaka Bay, in the Seto Inland Sea in Japan, in order to better understand the sedimentation processes operating on both terrestrial and marine organic matter in the Bay. The ¹³C and ¹⁵N of surface sediments in the estuary of the Yodo River were less than –23 and 5 respectively, but increased in the area up to about 10 km from the river mouth. At greater distances they became constant (giving ¹³C of about –20 and ¹⁵N about 6). It can be concluded that large amounts of terrestrial organic matter exist near the mouth of the Yodo River. Stable isotope ratios in the estuary of the Yodo River within 10 km of the river mouth were useful indicators allowing study of the movement of terrestrial organic matter. Deposition rates for total organic carbon (TOC) and total nitrogen (TN) over the whole of the Bay were estimated to be 63,100 ton C/year and 7,590 ton N/year, respectively. The deposition rate of terrestrial organic carbon was estimated to be 13,200 (range 2,000–21,500) ton C/year for the whole of Osaka Bay, and terrestrial organic carbon was estimated to be about 21% (range 3–34) of the TOC deposition rate. The ratio of the deposition rate of terrestrial organic carbon to the rate inflow of riverine TOC and particulate organic carbon (POC) were estimated to be 19% (range 3–31) and 76% (range 12–100), respectively.     

A Preliminary Study of Oceanic Bomb Radiocarbon Inventory in the North Pacific during the Last Two Decades

Radiocarbon and total carbonate data were obtained near the 1973 GEOSECS stations in the North Pacific along 30°N and along 175°E between 1993 and 1994. In these stations, we estimated radiocarbon originating from atomic bomb tests using tritium, trichlorofluoromethane and silicate contents. The average penetration depth of bomb radiocarbon during the two decades has deepened from 900 m to 1300 m. Bomb radiocarbon inventories above the average value for the whole North Pacific were found widely in the western subtropical region around 30°N both in the 1970s and 1990s, and its area in the 1990s was broader than that in the 1970s. In most of the North Pacific, while the bomb radiocarbon has decreased above 25.4, the bomb radiocarbon flux below 25.4 was over 1 × 10¹² atom m^-2yr^-1 in the subtropical region around 30°N. In the tropical area south of 20°N, the bomb radiocarbon inventory below 25.4 increased from zero to over 10 × 10¹² atom m^-2 during the last three decades. These distributions suggest that the bomb radiocarbon removed from the surface is currently accumulated with bomb ¹⁴C flux of over 1 × 10¹² atom m^-2yr^-1 below 25.4 in the subtropical region, mainly by advection from the higher latitude, and that part of the accumulated bomb ¹⁴C gradually spread southward with about 30 years.     

Variations in silicate concentration affecting photosynthetic carbon fixation by spring phytoplankton assemblages in surface water of the Strait of Malacca

The Strait of Malacca (SoM), the world’s busiest sea-route, is increasingly polluted as the rapid development of world trades, affecting phytoplankton primary productivity therein. The variations of surface phytoplankton biomass, size-structure and carbon fixation were investigated across the SoM during the spring period (May 4 to 9, 2011). Chlorophyll a concentration increased from 0.12 μg/L at the northwest entrance of the SoM to a maximal 0.63 μg/L at narrowest section, and decreased to 0.10 μg/L at the southeast entrance. Photosynthetic carbon fixation by phytoplankton coincided well with Chl a biomass, and increased from 10.8 to 22.3 μg C/(L d), then decreased to 9.21 μg C/(L d); while the carbon fixation rate showed an inverse pattern to the changes of Chl a, and decreased from 87.1 to 35.5 μg C/(μg Chl a d) and increased thereafter to 95.3 μg C/(μg Chla·d). Picophytoplankton cells (<3 μm) contributed to more than 60% and 50% of the total Chl a and carbon fixation at both the entry waters; while the contributions of pico-cells decreased sharply to the minimum of 18.3% and 27.5% at the narrowest part of the SoM. In particular, our results showed that the silicate concentration positively regulated Chl a biomass and carbon fixation, reflecting that the higher silicate favoured the growth of phytoplankton and thus led to higher primary production in this strait.     

大河影响下的边缘海沉积有机碳输运与埋藏及再矿化研究进展

大河影响下的边缘海是陆源输入物质的主要储库,也是有机碳埋藏和再矿化的主要场所,在全球碳的生物地球化学循环中有着重要作用。从有机碳的输运、埋藏和再矿化等方面综述了大河影响下的边缘海沉积有机碳生物地球化学研究的最新进展。研究表明,有机碳的来源、组成、粒径和密度分布等显著影响着有机碳的分布特征和归宿,大河影响下的边缘海中移动泥等特殊沉积环境在有机碳的输运、埋藏和再矿化分解等方面发挥了独特的作用;微生物分解作用则是边缘海沉积有机碳,特别是难降解陆源有机碳发生分解的重要因素。综合运用分子生物学、有机地球化学、生物地球化学等多学科研究手段,深入研究特定微生物、浮游生物功能类群等在大河影响下的边缘海沉积有机碳生物地球化学过程中的作用,将极大地丰富对河口和陆架边缘海生源要素生物地球化学循环的认识。     

中太平洋富钴结壳中生物标志物、有机碳同位素地球化学及其古海洋环境意义

利用2003年大洋DY105-12,14航次在中太平洋海山获取的KXD28富钴结壳样品,采用气相色谱(GC)内标法对该结壳样品的分层样进行了可溶有机质(氯仿沥青“A”)及其族组成(饱和烃、芳烃、非烃)、正构烷烃、类异戊二烯烃的定量分析,并结合总有机碳(TOC)及有机碳同位素(δ¹³C)分析,探讨了结壳样品有机质来源及富钴结壳组成与生长环境之间的关系。结果表明:(1)富钴结壳中有机质生物母源主要为海洋生物和菌藻类,并混有少量陆源物质;有机碳同位素同样也指示了海洋水生生物碳同位素特征;(2)KXD28结壳从底层到最外层有机碳同位素发生了很大变化,结壳中有机碳同位素组成变化与结壳生长过程中的海洋环境气候相符合:富钴结壳生长前期δ¹³C组成由正变负,对应全球气候变冷,南极底层流向太平洋挺进;而富钴结壳生长后期δ¹³C逐渐偏正,与全球气候变暖和南极底层流萎缩相关联。     

Impact of dynamic feedbacks between sedimentation,sea-level rise,and biomass production on near-surface marsh stratigraphy and carbon accumulation

Salt marshes accrete both organic and inorganic sediments. Here we present analytical and numerical models of salt marsh sedimentation that, in addition to capturing inorganic processes, explicitly account for above- and belowground organic processes including root growth and decay of organic carbon. The analytical model is used to examine the bias introduced by organic processes into proxy records of sedimentation, namely ¹³⁷Cs and ²¹⁰Pb. We find that accretion rates estimated using ²¹⁰Pb will be less than accretion rates estimated using the ¹³⁷Cs peak in steadily accreting marshes if (1) carbon decay is significant and (2) data for ²¹⁰Pb extend below the ¹³⁷Cs peak. The numerical model expands upon the analytical model by including belowground processes such as compaction and root growth, and by explicitly tracking the evolution of aboveground biomass and its effect on sedimentation rates. Using the numerical model we explore how marsh stratigraphy responds to sediment supply and the rate of sea-level rise. It is calibrated and tested using an extensive data set of both marsh stratigraphy and measurements of vegetation dynamics in a Spartina alterniflora marsh in South Carolina, USA. We find that carbon accumulation in marshes is nonlinearly related to both the supply of inorganic sediment and the rate of sea-level rise; carbon accumulation increases with sea-level rise until sea-level rise reaches a critical rate that drowns the marsh vegetation and halts carbon accumulation. The model predicts that changes in carbon storage resulting from changing sediment supply or sea-level rise are strongly dependent on the background sediment supply: if inorganic sediment supply is reduced in an already sediment poor marsh the storage of organic carbon will increase to a far greater extent than in a sediment-rich marsh, provided that the rate of sea-level rise does not exceed a threshold. These results imply that altering sediment supply to estuaries (e.g., by damming upstream rivers or altering littoral sediment transport) could lead to significant changes in the carbon budgets of coastal salt marshes.