云南富宁地区泥盆系—石炭系界线碳、氧同位素特征及对海平面变化的响应

右江盆地沉积连续的泥盆纪—石炭纪岩石地层,是中国泥盆纪与石炭纪之交Hangenberg生物大灭绝事件的重点研究区域。选取右江盆地西缘云南富宁地区晚泥盆世—早石炭世地层,在岩石地层学研究的基础上对碳酸盐岩进行系统的碳、氧同位素组成研究。富宁地区晚泥盆世—早石炭世地层存在不同幅度的δ13C、δ18O负向偏移,尤其在泥盆系—石炭系界线附近负偏移明显,δ13C、δ18O值偏移层位与层序地层学转换及古生物灭绝事件发生层位一致,反映了晚泥盆世法门期海平面下降和早石炭世的海侵事件。研究区泥盆系—石炭系界线附近δ13C值负偏趋势与右江盆地内δ13C值演化偏移相似,华南其他典型剖面δ13C值亦呈现不同幅度的负向偏移,泥盆纪与石炭纪之交的碳同位素演化序列与欧洲、北美地区δ13C值负向偏移反映的海平面下降事件一致,具全球性对比意义。     

Holocene environmental changes in the Whitefish Dunes Area, Door Peninsula, Northern Lake Michigan Basin, USA

A two meter sediment core taken from an inter-dune pond in Whitefish Dunes State Park, Door Peninsula, Wisconsin, provides a record of paleoenvironmental changes in the area from approximately 3600 RCYBP to 5100 RCYBP. The hydrology of the Whitefish Dunes pond is now apparently dependent on ground water recharge from local precipitation that infiltrates into the dunes and from Clark Lane, making it very sensitive to low magnitude, short term climate fluctuations.Changes in lithology, molluscan species diversity, oxygen isotopes from gastropod shells, and sediment organic content permit division of the core into several intervals representing different environmental regimes. The basal sediments are older than 5130 RCYBP and resemble those of the Liberty Grove Member of the Pleistocene Horicon Formation. The oldest Holocene sediments recorded in the core are an organic rich layer dated at 5130 RCYBP, which accumulated in a depression on the surface of a sand bar. Continued rise in the local water table during the Nipissing Transgression produced paludal conditions in the area, which were followed by the onset of lacustrine conditions. During this interval, the area supported a diverse molluscan fauna. Minor, short term climate fluctuations are reflected in sediment and oxygen isotope changes which are absent from the record in deep water cores from Lake Michigan. This phase in the history of the area ended with the eutrophication of the pond and the development of dunes. Information from Whitefish Dunes pond and other onshore sites within the Lake Michigan basin are an important source of data for reconstructing the history of water levels and climate changes for this area of the Great Lakes drainage.     

渐新世/中新世分界的地层学事件

介绍渐新世/中新世分界面(即古近纪/新近纪分界面)附近的浮游有孔虫和钙质超微化石事件及其新年龄。2004年国际地层年代表确定该分界面位于第58长偏心率周期弱振幅处,古地磁事件C6Cn.2n底面,经天文调谐后的年龄为23.03 Ma。发生在该界面附近的生物地层学事件主要是浮游有孔虫Paragloborotalia kugleri的始现面(22.96 Ma)和钙质超微化石Sphenolithus delphix的末现面(23.11 Ma)。在南海北部东沙群岛附近的大洋钻探ODP1148站,渐新世/中新世界面以崩塌沉积物为特征,有明显沉积间断,标志南海当时有较大范围的构造运动。     

九龙江河口区表层水铀同位素的粒级分布

利用微滤和超滤技术研究了九龙江河口区表层水中铀及其同位素组成的粒级分布和地球化学行为.结果表明,溶解态(<0.4μm)中低分子量组分(<10 000 u)占主要份额,胶体态(10 000 u~0.4μm)238U所占比例不足1%,且随盐度的增加其所占份额逐渐降低.溶解态、低分子量组分和胶体态238U的比活度与盐度之间存在良好的线性正相关关系,证实它们在九龙江河口区呈现保守行为.在颗粒态(>0.4μm)中,各粒级组分238U所占份额主要受控于相应颗粒物的浓度,在盐度小于20的区域,各粒级颗粒组分238U占颗粒态的份额有如下变化次序:10~53μm>2~10μm>0.4~2μm>大于53μm,而在盐度大于30的近外海站位,该次序发生一些变化:0.4~2μm>10~53μm>2~10μm>大于53μm,最小粒级颗粒组分238U的贡献有所增加,反映了自生铀贡献的加强.九龙江河口区表层水中溶解态(包括低分子量组分和胶体态)的234U/238U)_A.R.均大于1,显示出234U过剩的特征,而各粒级颗粒组分中的234U/238U)_A.R.则接近于平衡值(1.0).这一现象与陆地岩石风化过程中水体对铀的淋滤释出量及234U的优先浸出有关.对232Th/238U质量比的研究显示,溶解态及其所包括的低分子量组分和胶体态的232Th/238U质量比均小于1,而颗粒态及其所包括的4个粒级组分中的232Th/238U质量比均大于1,反映了向外海输送过程中铀、钍地球化学行为的差异.     

Factors influencing the oxidation,reduction, methylation and demethylation of mercury species in coastal waters

The objective of this study was to examine the redox reactions and other transformations of mercury (Hg) species in surface waters, and the factors determining the rates of these reactions. For the redox studies completed at the Chesapeake Biological Laboratory (CBL), two isotopes (¹⁹⁹Hg^II and ²⁰²Hg⁰) were added into different types of filtered water (fresh to seawater) to examine the oxidation and reduction reactions. Further studies of both the redox reactions and methylation/demethylation reactions of Hg were conducted with unfiltered water on board research vessels during cruises in May and July 2005 on the Chesapeake Bay and shelf. While CH₃¹⁹⁹Hg^II was added to allow the examination of demethylation, ²⁰¹Hg^II was used to examine both reduction and methylation, and ²⁰²Hg⁰ was used to examine oxidation. Overall, the results showed that both Hg oxidation and reduction were simultaneously occurring and were photochemically mediated in the waters investigated. In contrast to the previously assumed “unreactive” nature of Hg⁰, the studies found that the magnitude of the rate constant for Hg⁰ oxidation was greater than that for reduction, indicating its importance in estuarine and coastal waters. In addition, both experiments at CBL and on board ship showed that Hg^II reduction was similar in magnitude, suggesting that biotic processes were relatively unimportant. While no measurable methylation occurred during the incubation period during the on board studies, concentration of CH₃¹⁹⁹Hg^II decreased over the time during the experiments. It appeared that the demethylation processes were not dominantly photochemically driven, but could be microbially mediated. Further studies are needed in order to help better understand Hg redox and transformations in natural water systems.     

错流超滤技术在海水胶体态铀、钍、镭同位素和有机碳研究中的应用

建立了由预过滤装置、蠕动泵、中空纤维超滤膜(AmiconH10P10-20,标称截留分子量10KDa)和连接管组成的错流超滤系统,利用荧光标记的40KDa葡聚糖和已知放射性活度的234Th示踪剂评估了超滤膜的截留和吸附性质,探讨了234Th在超滤过程中的渗透行为,考查了该系统用于实际海水样品时铀、钍、镭同位素和有机碳的质量平衡状况.结果表明,10Kda中空纤维超滤膜对40Kda葡聚糖具有良好的截留效率(85%),而吸附损失率为18%.铀、钍、镭同位素和有机碳在超滤过程中均达到极佳的质量平衡,回收率R=95%～98%,优于大多数文献报道的值.234Th在超滤过程中的渗透行为可以很好地用渗透模型加以描述.研究组分胶体态含量占“溶解”态含量的份额大小顺序如下:钍同位素、有机碳、镭同位素约等于铀同位素,这与钍为强颗粒活性元素、铀和镭为水溶性元素的地球化学性质相吻合.     

Submarine groundwater discharge and benthic biogeochemical zonation in the Huanghe River Estuary

Submarine groundwater discharge(SGD) has received increasing attention by studies on coastal areas; however,its effects on biogeochemical zonation have not been investigated to date. The Huanghe River Estuary(HRE) is a world class river estuary with high turbidity, and heavy human regulation. This study investigated how SGD is related to the benthic biogeochemistry of the HRE. Based on the distribution of several parameters(e.g., salinity,temperature, dissolved oxygen(DO) levels, p H, radium iso...     

Using triple oxygen isotopes and oxygen-argon ratio to quantify ecosystem production in the mixed layer of northern South China Sea slope region

Quantifying the gross and net production is an essential component of carbon cycling and marine ecosystem studies.Triple oxygen isotope measurements and the O_2/Ar ratio are powerful indices in quantifying the gross primary production and net community production of the mixed layer zone,respectively.Although there is a substantial advantage in refining the gas exchange term and water column vertical mixing calibration,application of mixed layer depth history to the gas exchange term and its contribution to reducing indices error are unclear.Therefore,two cruises were conducted in the slope regions of the northern South China Sea in October 2014(autumn) and June 2015(spring).Discrete water samples at Station L07 in the upper 150 m depth were collected for the determination of δ~(17)0,δ~(18)O,and the O_2/Ar ratio of dissolved gases.Gross oxygen production(GOP) was estimated using the triple oxygen isotopes of the dissolved O_2,and net oxygen production(NOP) was calculated using O_2/Ar ratio and O_2 concentration.The vertical mixing effect in NOP was calibrated via a N_2O based approach.GOP for autumn and spring was(169±23) mmol/(m~2·d)(by O_2) and(189±26) mmol/(m~2·d)(by O_2),respectively.While NOP was 1.5 mmol/(m~2·d)(by O_2) in autumn and 8.2 mmol/(m~2·d)(by O_2) in spring.Application of mixed layer depth history in the gas flux parametrization reduced up to 9.5% error in the GOP and NOP estimations.A comparison with an independent O_2 budget calculation in the diel observation indicated a26% overestimation in the current GOP,likely due to the vertical mixing effect.Both GOP and NOP in June were higher than those in October.Potential explanations for this include the occurrence of an eddy process in June,which may have exerted a submesoscale upwelling at the sampling station,and also the markedly higher terrestrial impact in June.     

Determination of residence time and mixing processes of the Ubatuba,Brazil, inner shelf waters using natural Ra isotopes

Coastal waters contain elevated dissolved activities of short-lived radium isotopes, ²²³Ra and ²²⁴Ra, having half-lives of 11.4 and 3.66 days, respectively. The input of these isotopes near the coast must be balanced by decay and mixing into the open ocean, where excess activities are zero. Since the decay rate is known, in the ideal case the mixing rate may be determined from the offshore distribution of these isotopes. This study found that samples collected in June 2000 followed the expected exponential decrease with distance offshore. We assign a dispersion coefficient of 28–39 m² s⁻¹ for this study. During January 2002 and November 2003, there was not a consistent decrease of activity with distance offshore. This is likely due to the ruggedness of the coastline, where many bays and small islands interrupt simple mixing patterns. To estimate exchange rates during 2002 and 2003, we used a model based on the decrease in the ²²⁴Ra/²²³Ra activity ratio (AR) with time for samples isolated from fresh inputs of Ra. This model yielded residence times of 1–2 weeks for samples collected within 20 km of the coast. We used this residence time to calculate the flux of ²²⁸Ra (half-life = 5.7 years) to the study area necessary to maintain the enrichment relative to ocean water. This enrichment is a factor of ten greater than the flux of ²²⁸Ra expected from submarine groundwater discharge (SGD) occurring within 50 m of shore.