乌裕尔河流域颗粒有机碳的来源：碳同位素证据

以2008、2009年所采集的乌裕尔河9个点位水体中的悬浮物为研究对象,对丰、枯水期颗粒有机碳（POC）含量、碳同位素组成（^13C、^14C）及表观年龄进行了系统测试与分析,以期探讨河流中颗粒有机碳来源与流域土壤侵蚀的关系。研究结果表明,该河流中颗粒有机碳（POC）主要来源于未受玉米残体及根系输入影响的深层土壤,且土...     

珠江水体悬浮物碳稳定同位素组成与流域土壤侵蚀研究

以珠江流域水体悬浮物为研究对象,对其碳稳定同位素组成(δ13C)及颗粒有机碳(POC)的含量进行了测定和研究。结果表明:河流悬浮物同位素组成与珠江流域植被分布格局、土壤有机质密切相关;珠江悬浮物碳同位素组成主要受C3植被影响,其中,西江悬浮物碳同位素组成表现出较强的C4植被特征。东江水体悬浮物碳同位素组成在洪水季节表现出较强的C4植被特征,其它季节则表现出C3植被特征;北江水体悬浮物碳同位素组成无明显的C4植被特征。东江悬浮物样品POCδ13C值呈逐年上升趋势,与近年来流域内植被破坏和土壤侵蚀加剧相对应,并显示其侵蚀程度超过西江流域。     

Temporal variation and fluxes of dissolved and particulate organic carbon in the Apure,Caura and Orinoco rivers,Venezuela

The concentrations of total suspended sediments (TSS), dissolved organic carbon (DOC) and particulate organic carbon (POC) were measured in water samples taken monthly in the Apure, Caura and Orinoco rivers during a hydrological cycle (between Sept. 2007 and Aug. 2008). The DOC concentration values ranged between 1.5 and 6.8 mgC l⁻¹ in the Apure River; 2.07 and 4.9 mgC l⁻¹ in the Caura River and 1.66 and 5.35 mgC l⁻¹ in the Orinoco River. The mean concentration of DOC was 3.9 mgC l⁻¹ in the Apure River, 3.24 mgC l⁻¹ in the Caura River and 2.92 mgC l⁻¹ in the Orinoco River at Puerto Ordaz. The three rivers showed a similar temporal pattern in the concentrations of DOC, with higher DOC values during the increasing branch of the hydrograph due to wash-out processes of the organic material stored in soils. The mean concentration values of POC were 1.33 mgC l⁻¹; 0.77 mgC l⁻¹ and 0.91 mgC l⁻¹ in the Apure, Caura and Orinoco rivers, respectively. The inverse relationship found between the percentage in weight of the POC and the concentrations of TSS in the three rivers fits a logarithmic model, as it has been previously reported for other worldwide rivers. The POC concentrations in the Orinoco River showed a positive relationship with the TSS, suggesting that the POC in the Orinoco is the result of terrestrially organic matter. Although the fluxes of organic carbon (OC) in the three studied rivers are dependent on the values of water discharge, the fluxes of DOC during the increasing branch of the hydrograph are higher than those found during the decreasing stage, due to the yield of organic material accumulated in soils during the preceding dry season. The mean annual flux of total organic carbon (TOC) of the Orinoco River at Puerto Ordaz was about 4.27 × 10⁶ TonC yr⁻¹. Of this, 3.28 × 10⁶ TonC yr⁻¹ (77%) represents the flux of DOC and about 0.99 TonC yr⁻¹ (23%) represents the flux of POC. The mean annual input of TOC from the Apure River to the Orinoco River was about 4.92 × 10⁵ TonC yr⁻¹ (11.5%), while the contribution of TOC from the Caura River to the Orinoco River was estimated at 3.05 × 10⁵ TonC yr⁻¹ (7.1%).The values of annual transport of TOC calculated for the Apure, Caura and Orinoco rivers were lower than those reported twenty years ago. This could be related to interannual variations of precipitation in the Orinoco Basin, due to runoff variations can have a strong effect on the fluxes of OC from land to rivers.     

Transport of particulate organic carbon by the Mississippi River and its fate in the Gulf of Mexico

This study was designed to determine the amount of particulate organic carbon (POC) introduced to the Gulf of Mexico by the Mississippi River and assess the influence of POC inputs on the development of hypoxia and burial of organic carbon on the Louisiana continental shelf. Samples of suspended sediment and supporting hydrographic data were collected from the river and >50 sites on the adjacent shelf. Suspended particles collected in the river averaged 1.8±0.3% organic carbon. Because of this uniformity, POC values (in μmol l^?1) correlated well with concentrations of total suspended matter. Net transport of total organic carbon by the Mississippi-Atchafalaya River system averaged 0.48×10¹² moles y^?1 with 66% of the total organic carbon carried as POC. Concentrations of POC decreased from as high as 600 μmol l^?1 in the river to <0.8 μmol l^?1 in offshore waters. In contrast, the organic carbon fraction of the suspended matter increased from <2% of the total mass in the river to >35% along the shelf at ≥10 km from the river mouth. River flow was a dominant factor in controlling particle and POC distributions; however, time-series data showed that tides and weather fronts can influence particle movement and POC concentrations. Values for apparent oxygen utilization (AOU) increased from ～60 μmol l^?1 to >200 μmol l^?1 along the shelf on approach to the region of chronic hypoxia. Short-term increases in AOU were related to transport of more particle-rich waters. Sediments buried on the shelf contained less organic carbon than incoming river particles. Orgamic carbon and δ¹³C values for shelf sediments indicated 3 that large amounts of both terrigenous and marine organic carbon are being decomposed in shelf waters and sediments to fuel observed hypoxia.     

A depositional history of particulate organic carbon in a floodplain lake from the lower Ob’ River, Siberia

Northern, high latitude soils have stored vast amounts of organic carbon (OC) in permafrost and peats for many millennia, however, climate change may mobilize and release this particulate OC (POC) to arctic rivers. Deltaic and floodplain lakes that receive fluvial sediments, primarily during the spring freshet, may provide records of such changes in riverine POC. Here, we examine properties of OC in a sediment core from a lake in the lower floodplain of the Ob’ River, west Siberia, to determine how the properties of OC deposited in this lake varied over many decades and to evaluate use of this sedimentary OC as a recorder of riverine POC load and properties. The core predates the most recent, dramatic changes in arctic climate and hence may serve as a benchmark against which to contrast future variations in fluvial POC discharge. Elemental, stable carbon and radiocarbon isotopic analyses, along with nuclear magnetic resonance (NMR) spectroscopy and molecular-level information (lignin phenol composition), indicate two major sources of OC to most of the sediments in this lake: plant-derived OC and algal-derived OC. However, a mixing model indicates that the nature and ¹⁴C content of these two sources change with depth in the sediment, resulting in three distinct layers: surface horizons, a “high-OC” layer and “mixing” horizons found above and below the high-OC layer. The plant-derived component is significantly aged throughout the core (¹⁴C ages of 1300-3900 years) and appears to derive from primarily local, tundra sources, whereas the algal component is modern. Our analysis suggests that the usual mode of OC deposition, as exemplified by the “mixing” and surface horizons, involved mixing of varying amounts of new algal production (35-65%) with aged permafrost- or peat-derived OC. This deposition was interrupted by an event, such as the collapse of a riverbank, which laid down the compositionally distinct “high-OC” layer in which plant-derived OC mixes with aged mineral-soil-derived OC without clear input from algae. The relative amounts of the plant and algal components in the lake sediments appear to be controlled primarily by local hydrological conditions rather than by river-wide processes, suggesting that comparison of sediment records from multiple lakes within a floodplain will be important to assess changes in POC export by arctic rivers. However, the flux and nature of the higher plant-derived OC may carry important information on the sources and dynamics of OC stored within the drainage basin.     

Total organic carbon transport by the Alaknanda River,Garhwal Himalayas,India

Transport and fate of organic carbon by the fluvial system play a significant role in the global biogeochemical cycle of carbon. Previous studies show that the transportation of modern organic carbon from the Himalayan River system accounts for 10–20% of the total global flux to the oceans. Till date, no study has been published which dealt with the transport of organic carbon in the headwaters of the Ganga River. The Alaknanda River is a headwater stream of the Ganga, which flows in the Western Himalayas of India. Water and freshly deposited channel sediment samples were collected during the months of March 2014 and August 2014 and analysed for dissolved organic carbon (DOC), particulate organic carbon (POC) and channel organic carbon (COC). The observed variability of organic carbon concentration was correlated with factors such as discharge, physiography and suspended sediment concentration (SSC). The results show that seasonal erosivity in the basin influences its DOC concentration and physiography, thus acting as a key parameter which controls transportation, oxidation and residence time of the organic matter. The allochthonous input of sediments from the erosional activities is the major source of organic carbon. At Devprayag, Alaknanda contributes 66% of the total DOC flux carried by the Ganga River. The comparison with the previously published values indicate that due to differences in physiography and chemical weathering rate, the Ganga River transports organic carbon mainly as a dissolved load in its upstream and predominantly as POC down the Himalayan foothills.     

Determination of mercury biogeochemical fluxes in the remote Mackenzie River Basin,northwest Canada,using speciation of sulfur and organic carbon

The Mackenzie River Basin (MRB) in NW Canada is one of the least human-impacted large watersheds in the world. The western and eastern sub-basins of the MRB are also marked by contrasting geology, geomorphology, hydrology, and biology. These remarkable differences in a remote river basin provide a unique opportunity to probe the biogeochemical processes governing the sources, transport, and bioavailability of Hg at the terrestrial-marine interface and ultimately in the Arctic Ocean. Based on a large dataset of the concentration and speciation of Hg, S and organic matter in surface sediments across the MRB, a source-apportioned budget was constructed for Hg in the MRB. The results indicate that the Hg flux in the basin originates primarily from the weathering of sulfide minerals in the western mountainous sub-basin (∼78% of the total), followed by the erosion of coal deposits along the mainstream of the Mackenzie River (∼10%), with the remainder split between atmospheric inputs and organic matter-bound Hg (6% and 5%, respectively). Although the Hg flux from the eastern peatland sub-basin only accounts for ∼10% of the total riverine Hg flux, Hg in this region correlates strongly with labile organic matter, and will likely have a much stronger influence on local biota.     

Sedimentation of particulate matter in the Dona Paula Bay, West Coast of India during November to May 1995–1997

Data on hydrography, nutrients, suspended particles, and sedimented particles were collected at weekly intervals from November to May during 1995 to 1997 at a station in the coastal waters of Dona Paula Bay, India. Suspended and sedimented particles were analyzed for total suspended matter (SPM), total sedimented particulate matter (TPM), particulate organic carbon (POC), particulate organic nitrogen (PON), chlorophylla (chla), and diatom abundance. Variations in hydrography and nutrients influenced the quantity and composition of sedimented particles. The TPM, POC, PON, and chla fluxes showed small-scale seasonal variations and were higher in the summer (February to May) than in the winter (November to January). Resuspension of carbon accounted for approximately 25% of the gross POC and was highest in April 1997 (45%). The mean net POC flux was 197±90 mg C m⁻² d⁻¹ and accounts for 4.6% of the TPM. The average C∶N (w∶w) ratio of the sedimented material was 13.2±6.6. The POC:chla ratio was relatively higher in the sedimented material as compared to the suspended material. The particulate carbon reaching the bottom sediment was 39% of the primary production. The low organic carbon concentration (approximately 0.1% of dry sediment) in the sediments implies that about 98% of the sedimented carbon was either consumed at the sedimentwater interface or resuspended/advected before it was finally buried into the sediments.     

Potential source rocks, organic geochemistry and thermal maturation in the southern depocenter (Kipourio–Grevena) of the Mesohellenic Basin, central Greece

The study area is the southern depocenter (depth > 4200 m) of the Mesohellenic Basin which extends between Kipourio and Grevena, central Greece. The Mesohellenic Basin is a Middle-Tertiary intramontane basin developed within the Hellenide orogen. Previous studies have focused on the depositional environments, configuration and hydrocarbon potential of the basin. In this paper we present additional geochemical and petrographic data from outcrop samples of the basin's southern depocenter, which is considered the most promising area, in terms of hydrocarbon prospectivity. A total number of thirty six samples were analysed: Rock-Eval pyrolysis, maceral analysis, vitrinite reflectance and thermal alteration index, bitumens extraction, liquid chromatography, and GC-MS. The samples were collected from deltaic deposits and submarine fan sediments of Late Eocene to Late Oligocene age. The TOC values of the analysed samples range between rich and very rich and the organic matter consists mainly of type III kerogen and the organic matter consider to be predominately gas prone. The thermal maturity assessed from T_max and vitrinite reflectance shows an immature stage of the organic matter along with the presence of layers having reached the very early mature stage. Vitrinite reflectance measurements and maturity calculations (applying the Lopatin modeling), reveal that the lower part of the depocenter sediments falls within the ‘oil window’. The extractable organic matter (EOM) (mg bitumens/g TOC) indicate the existence of samples (from deltaic deposits) with high ratio of transformation (EOM) (> 100 mg bitumen/g TOC). The GC and GC-MS analyses of the biomarkers indicate mainly the occurrence of terrestrial organic matter reflecting oxidizing conditions and both immature and very early mature stages. The results of the Rock-Eval pyrolysis and the distribution of the isoprenoids support the assumption of the input of an organic matter mixture.     

Abundance and Chemical Speciation of Phosphorus in Sediments of the Mackenzie River Delta, the Chukchi Sea and the Bering Sea: Importance of Detrital Apatite

Utilizing a sequential extraction technique this study provides the first quantitative analysis on the abundance of sedimentary phosphorus and its partitioning between chemically distinguishable phases in sediments of the Bering Sea, the Chukchi Sea and the Mackenzie River Delta in the western Arctic Ocean. Total sedimentary phosphorus (TSP) was fractionated into five operationally defined phases: (1) adsorbed inorganic and exchangeable organic phosphorus, (2) Fe-bound inorganic phosphorus, (3) authigenic carbonate fluorapatite, biogenic apatite and calcium carbonate-bound inorganic and organic phosphorus, (4) detrital apatite, and (5) refractory organic phosphorus. TSP concentrations in surface sediments increased from the Chukchi Sea (18 μmol g⁻¹ of dried sediments) to the Bering Sea (22 μmol g⁻¹) and to the Mackenzie River Delta (29 μmol g⁻¹). Among the five pools, detrital apatite phosphorus of igneous or metamorphic origin represents the largest fraction (~43%) of TSP. The second largest pool is the authigenic carbonate fluorapatite, biogenic apatite as well as CaCO₃ associated phosphorus (~24% of TSP), followed by the Fe-bound inorganic phosphorus, representing ~20% of TSP. The refractory organic P accounts for ~10% of TSP and the readily exchangeable adsorbed P accounts for only 3.5% of TSP. Inorganic phosphorus dominates all of phosphorus pools, accounting for an average of 87% of the TSP. Relatively high sedimentary organic carbon and total nitrogen contents and low δ¹³C values in the Mackenzie River Delta together with the dominance of detrital apatite in the TSP demonstrate the importance of riverine inputs in governing the abundance and speciation of sedimentary phosphorus in the Arctic coastal sediments.     

Temporal variability in terrestrially-derived sources of particulate organic carbon in the lower Mississippi River and its upper tributaries

In this study, we examined the temporal changes of terrestrially-derived particulate organic carbon (POC) in the lower Mississippi River (MR) and in a very limited account, the upper tributaries (Upper MR, Ohio River, and Missouri River). We used for the first time a combination of lignin-phenols, bulk stable carbon isotopes, and compound-specific isotope analyses (CSIA) to examine POC in the lower MR and upper tributaries.A lack of correlation between POC and lignin phenol abundances (Λ₈) was likely due to dilution effects from autochthonous production in the river, which has been shown to be considerably higher than previously expected. The range of δ¹³C values for p-hydroxycinnamic and ferulic acids in POC in the lower river do support that POM in the lower river does have a significant component of C₄ in addition to C₃ source materials. A strong correlation between δ¹³C values of p-hydroxycinnamic, ferulic, and vanillyl phenols suggests a consistent input of C₃ and C₄ carbon to POC lignin while a lack of correlation between these same phenols and POC bulk δ¹³C further indicates the considerable role of autochthonous carbon in the lower MR POC budget. Our estimates indicate an annual flux of POC of 9.3 × 10⁸ kg y⁻¹ to the Gulf of Mexico. Total lignin fluxes, based on Λ₈ values of POC, were estimated to be 1.2 × 10⁵ kg y⁻¹. If we include the total dissolved organic carbon (DOC) flux (3.1 × 10⁹ kg y⁻¹) reported by [Bianchi T. S., Filley T., Dria K. and Hatcher, P. (2004) Temporal variability in sources of dissolved organic carbon in the lower Mississippi River. Geochim. Cosmochim. Acta68, 959-967.], we get a total organic carbon flux of 4.0 × 10⁹ kg y⁻¹. This represents 0.82% of the annual total organic carbon supplied to the oceans by rivers (4.9 × 10¹¹ kg).     

Suspended sediments and organic matter in mountain headwaters of the Amazon River: Results from a 1-year time series study in the central Peruvian Andes

Few studies have examined the dynamics of sediments and suspended organic matter and their export from headwater basins in the Andes Mountains to the Amazon River, despite the fact that the Andes are the primary source of sediments to the lower Amazon basin. We measured river discharge as well as the concentration, δ¹⁵N, δ¹³C, %N, and %OC of coarse and fine suspended sediments (CSS and FSS) in the Chorobamba River, located in the central Andean Amazon of Peru. Samples were taken at least weekly over an entire year (July 2004-July 2005), with additional sampling during storms. Concentrations of particulate organic matter (POM) were generally low in the study river, with concentrations increasing by up to several orders of magnitude during episodic rain events. Because both overall flow volumes and POM concentrations increased under stormflow conditions, the export of POM was enhanced multiplicatively during these events. We estimated that a minimum of 80% of annual suspended sediment transfer occurred during only about 10 days of the year, also accounting for 74% of particulate organic carbon and 64% of particulate organic nitrogen transport. Significant differences occurred between seasons (wet and dry) for δ¹³C of coarse and fine POM in the Chorobamba River, reflecting seasonal changes in organic matter sources. The time series data indicate that this Andean river exports approximately equal amounts of fine and coarse POM to the lower Amazon. The observation that the vast majority of sediments and associated OM exported from Andean rivers is mobilized during short, infrequent storm events and landslides has important implications for our understanding of Amazon geochemistry, especially in the face of incipient global change.     

Dissolved Trace Metal–Organic Complexes in the Lot–Garonne River System Determined Using the C18 Sep-Pak System

An 11-month observation of dissolved and particulate organic matter, chlorophyll a(Chl a), C18 Sep-Pak extractable hydrophobic dissolved organic matter (hDOM) fraction and associated dissolved trace metals (Cd, Cu, V, Co, Ni, Mo, U) was performed in the Lot–Garonne River system. This system includes the Riou Mort, the Lot River and the downstream reaches of the Garonne River and represents the fluvial transport path of trace metals between the major point source of polymetallic pollution, located in the Riou Mort watershed and the Gironde estuary. Spatial and temporal variations of dissolved and particulate organic carbon and Chl areflect the presence of different types of organic matter and their relation with the hDOM fraction. Maximum Chl a/POC ratios (up to 0.03), indicate intense phytoplankton production from March to May. In the Lot River (Temple), DOC and POC concentrations were clearly higher and mean Chl a concentration (2.8 mg g⁻¹) was about three times higher than those of the other sites. High Chl a/POC ratios suggest high phytoplankton activity with maxima in spring and late summer. In the Riou Mort River, very high POC concentrations of up to 40 (mean: 20) occurred, whereas Chl a concentrations were relatively low indicating low phytoplankton activity. High, strongly variable DOC and POC concentrations suggest important natural (Carboniferous soils, forests) or anthropogenic (e.g., former coal mines, waste areas, agriculture, sewage) carbon sources within the small Riou Mort watershed. Despite high DOC concentrations in the Riou Mort River, hDOM metal fractions were generally lower than those at the other sites. The general order of decreasing binding strength between metals and the organic hydrophobic phase (Cu, U > Co, Ni > V, Mo > Cd) at all four sites was in good agreement with the Irving–William series of transition element affinity towards organic ligands. Accordingly, the role of the hydrophobic phase in dissolved Cd transport appeared to be negligible, whereas the hDOM–Cu fraction strongly contributed to dissolved Cu transport.     

Sources,sinks and distribution of organic carbon in the St. Lawrence Estuary,Canada

Carbon isotope ratio analysis of particulate, planktonic, and sedimentary organic carbon and dissolved inorganic carbon has been used to study the sources and sinks of the organic carbon in the St. Lawrence Estuary and Gulf of St. Lawrence, Canada. Particulate organic carbon (POC) isotope ratios in the upper St. Lawrence Estuary are uniform and indistinguishable from those of POC in the St. Lawrence River and of planktonic organic carbon in both areas. The abundance of freshwater diatoms in the upper Estuary suggests that upper Estuary POC is predominantly “fresh” organic matter of riverborne origin. Upper Estuary POC is isotopically different from POC in the lower St. Lawrence Estuary and Gaspé regions, but is not different from POC from the surface waters of the open Gulf of St. Lawrence. The isotopic composition of planktonic organic carbon mirrors that of the POC, indicating that the POC in the lower Estuary and Gulf is also “fresh” organic matter. Since the lower Estuary POC forms an isotopic barrier between the upper Estuary POC and the Gulf of St. Lawrence POC, there appears to be little mixing of POC between these three reservoirs. Therefore POC in the lower Estuary and Gulf is most likely both produced and deposited (or degraded) in situ.An examination of carbon isotope ratio differences between the planktonic and dissolved inorganic carbon reservoirs shows that this difference varies significantly and somewhat unpredictably between sectors of the study area. Interpretation of environmental carbon isotope data on the basis of an assumed, constant fractionation factor may be subject to large errors. Direct measurement of both reservoirs is obviously preferable.     

Modern carbon burial in Lake Qinghai,China

The quantification of carbon burial in lake sediments, and carbon fluxes derived from different origins are crucial to understand modern lacustrine carbon budgets, and to assess the role of lakes in the global carbon cycle. In this study, we estimated carbon burial in the sediment of Lake Qinghai, the largest inland lake in China, and the carbon fluxes derived from different origins. We find that: (1) The organic carbon burial rate in lake sediment is approximately 7.23 g m⁻² a⁻¹, which is comparable to rates documented in many large lakes worldwide. We determined that the flux of riverine particulate organic carbon (POC) is approximately 10 times higher than that of dissolved organic carbon (DOC). Organic matter in lake sediments is primarily derived from POC in lake water, of which approximately 80% is of terrestrial origin. (2) The inorganic carbon burial rate in lake sediment is slightly higher than that of organic carbon. The flux of riverine dissolved inorganic carbon (DIC) is approximately 20 times that of DOC, and more than 70% of the riverine DIC is drawn directly and/or indirectly from atmospheric CO₂. (3) Both DIC and DOC are concentrated in lake water, suggesting that the lake serves as a sink for both organic and inorganic carbon over long term timescales. (4) Our analysis suggests that the carbon burial rates in Lake Qinghai would be much higher in warmer climatic periods than in cold ones, implying a growing role in the global carbon cycle under a continued global warming scenario.     

Sources and pathways of natural and anthropogenic hydrocarbons into the natural dump Arkona Basin (southern Baltic Sea)

 Surface sediments, suspended particulate matter and fluffy-layer material, collected in the Arkona Basin and the Pomeranian Bay during 1995–1997, as well as air particulate matter, collected on the island of Rügen during August 1995, were analysed for total organic carbon content, saturated and polycyclic aromatic hydrocarbons (PAH). The resulting concentrations and distributions of these compounds and molecular PAH ratios are discussed in terms of matrix, origin of the organic matter and seasonal variations. The data show that the Oder river can be identified as a major source for PAH transported into the southern part of the Arkona Basin. A strong atmospheric input of PAH is noted for the central and northern part of the basin. In general, anthropogenic and bacterially degraded hydrocarbons bound to organic carbon-rich and small particles are mainly deposited in the basin center, whereas their natural counterparts accumulate mainly on the basin flanks covered by coarser grained sediments. Received: 2 March 1999 · Accepted: 8 June 1999     

Early Holocene sea level in the Canadian Beaufort Sea constrained by radiocarbon dates from a deep borehole in the Mackenzie Trough,Arctic Canada

Deglacial and Holocene relative sea level (RSL) in the Canadian Beaufort Sea was influenced by the timing and extent of glacial ice in the Mackenzie River corridor and adjacent coastal plains. Considerable evidence indicates extensive ice cover in this region of northwestern Canada during the Late Wisconsinan. However, no absolute ages exist to constrain maximum RSL lowering before the late Holocene (4.2–0 ka). In 1984, the Geological Survey of Canada drilled an 81.5‐m‐deep borehole in the western Mackenzie Trough at 45 m water depth (MTW01). The lower 52.5 m of the borehole was interpreted as a deltaic progradational sequence deposited during a period of rising sea level. The upper 29 m was described as foraminifer‐bearing marine sediments deposited after transgression of the site, when RSL rose above ~−74 m. Here, we present radiocarbon measurements from MTW01, acquired from benthic foraminifera, mollusc fragments and particulate organic carbon in the >63 μm fraction (POC_{>63 μm}) in an attempt to constrain the chronology of sediments within this borehole and date the timing of transgression. The deepest carbonate macrofossil was acquired from 8 m above the transgressive surface (equivalent to 21 m b.s.l.), where mollusc fragments returned a date of 9400 +180–260 cal. a BP (2σ). This provides the oldest constraint on Holocene sea‐level lowering in the region, and implies that transgression at this site occurred prior to the early Holocene. Ages obtained from the lower 52.5 m of the borehole are limited to POC_>63 μm samples. These indicate that progradational sediments were deposited rapidly after 24 820 +390–380 cal. a BP (2σ). Due to the incorporation of older reworked organic matter, the actual age of progradation is likely to be younger, occurring after Late Wisconsinan glacial ice retreated from the coast.     

黄河口有机碳的时空输运特征及其影响因素分析

通过2004年4月,2004年9月,2005年9月,2006年4月4个航次,结合2003年8月对河道感潮带的连续同步观测,对低流量下黄河口有机碳的输运特征进行了考察。结果发现:黄河输入至河口的悬浮物中颗粒有机碳(POC)含量约为0.51%,主要以陆源输入为主,几乎不受季节变化影响,由于大量POC含量低的陆源泥沙的稀释作用,浮游植物对总颗粒有机碳的贡献只有在悬浮物含量(TSS)<200mg/L时才能显现出来;黄河口TSS超过455mg/L时,有机碳入海以颗粒有机碳为主;反之,以溶解有机碳为主。黄河口悬浮物在低盐度区沉降作用前后的中值粒径降低,Φ>16μm的悬浮物的沉降作用比Φ<16μm的悬浮物更为剧烈,POC含量随悬浮物粒径的降低而升高,黄河携带的颗粒有机碳80%以上集中在Φ<16μm的TSS中;低流量下,黄河口最大混浊带对POC的过滤效率为65%,混浊带对POC的过滤效应能造成黄河口POC的有效通量被高估;由于受黄河口沉积物向水体解析DOC的影响,在盐度小于10时,DOC几乎不受海水稀释作用的影响,但在盐度大于10的区域DOC与盐度表现出良好的负相关关系,黄河口枯、丰水期淡水端溶解有机碳的有效浓度分别高于实测最高值20%和10%左右,从而造成黄河口DOC有效通量被低估。     

Distribution of particulate carbohydrate species in the Bay of Bengal

Suspended particulate matter (SPM) of surface seawaters was collected during December 2003 to October 2004 at 10 stations in the Bay of Bengal, and analyzed for particulate organic carbon (POC), total particulate nitrogen (TPN), total particulate carbohydrate (TPCHO) and total particulate uronic acids (TPURA). The concentrations of POC, TPCHO and TPURA varied from 4.80 to 29.12, 0.85 to 4.24, 0.09 to 0.91 μM C, respectively. The TPCHO-C and TPURA-C accounted for 6.6–32.5% and 0.87–3.65% of POC. The trends observed for the distribution of these compounds were generally similar to those recorded for the distribution of chlorophyll a (Chl a). The C/N ratios varied from 3.2 to 22.3 with most of the values being < 10. This suggests that the organic matter was mostly derived from phytoplankton and bacteria. Relatively low C/N ratios and high TPCHO yield imply that freshly derived organic matter was present during SWM and FIM. Our data suggest that the quality and quantity of organic matter varied spatially and seasonally.     

基于泥沙中碳含量的变化表征黄河调水调沙入海泥沙的扩散范围

主要通过黄河口悬浮物中有机碳和无机碳的含量,表征黄河调水调沙入海的泥沙在黄河口外近海的扩散范围。结果表明:黄河口入海前泥沙中的颗粒无机碳(PIC),颗粒有机碳(POC)具有稳定性,分别为(1.75×0.28)%和(0.51×0.08)%;在悬浮物含量约为30 mg/L时,黄河口临近海区悬浮物中的PIC、POC含量分别出现突跃性降低和升高趋势,叶绿素分析表明,POC含量的升高是由于浮游植物对颗粒有机碳贡献的结果,同时正构烷烃轻重比值ΣC₂₀-/ΣC₂₀+和碳优势指数(CPI)值也分别增加和降低;X衍射发现悬浮物浓度低于30 mg/L时,黄河泥沙在悬浮物中所占比例迅速下降,从而造成悬浮物中PIC突跃性下降;因此,黄河口近海悬浮物含量30 mg/L可以被认为是陆源和海源颗粒物对黄河口近海区悬浮物贡献的有效分界线。调水调沙入海的泥沙在黄河口外近海表层主要扩散到河口以南海域,而底层扩散范围主要集中在河口以北和河口以南海域,这些泥沙最终可能停留在莱州湾中部。