长江口区海水中溶解有机碳和颗粒有机碳的分布及变化的研究

长江每年有上千万吨有机物质注入河口邻近海域，影响着这一海域独特的生态环境。 本文根据1985年8月至1986年5月专业调查资料,论述了长江口邻近海域溶解有机碳(DOC)和颗粒有机碳(POC)的分布及变化，并从有机物质的变化推测三峡工程对河口海生态系的影响。     

Influence of winds and oceanographic conditions on the mucilage aggregation in the Northern Adriatic Sea in 2003–2006

Meteorological and oceanographic conditions in the Northern Adriatic Sea in a year notable for massive mucilage formation (2004) were compared with those in years where this phenomenon did not occur (2003, 2005 and 2006) to suggest possible links. The months preceding the mucilage event in 2004 were considered the ‘incubation period’ and were characterized by a strong freshet in May which increased the water column stability. Winter cooling and scarcity of freshwater inputs from the Po River triggered the dense water formation and intrusion in the northern basin. Weak southeasterly winds and an increase in surface seawater temperatures contributed to maintain and reinforce the water column stability, and at the same time an intense diatom spring bloom created the conditions for accumulation of organic matter. The interplay of climatological forcings and biological processes caused temporal variations of dissolved organic carbon (DOC) and particulate organic carbon (POC) in the basin, with POC playing an important role in the aggregation process, as suggested by its increase relative to DOC before massive mucilage formation. We therefore suggest that high POC/total particulate nitrogen ratios in the suspended particulate organic fraction, a steep increase of POC/Chlorphyll a, and the decreased DOC/POC ratios represent ‘early warning’ signals of the main processes that lead to mucilage events in the Northern Adriatic Sea.     

Effect of wood waste dumping on organic matter in seawater and surficial sediments of Alberni Inlet,British Columbia

Distribution of particulate organic carbon (POC) and dissolved organic carbon (DOC) in seawater, and chemical composition of surficial sediments were studied in relation to pulpmill effluent and dumping of dredge spoil containing wood debris in Alberni Inlet, British Columbia, Canada. The maximum concentration of POC (377–584µg Cl^–1) was observed at the surface around the dumping area (5–7 km seaward of the inlet's head), and at the location immediately adjacent to the dump site POC was elevated throughout the water column (50 m). While POC tended to decrease in the surface layer for a distance of about 25km down-inlet, measureable effects of POC in the deeper water did not extend beyond 600m from the dump site. The dump site was conspicuous by the large maximum in C:N ratio (46.3). In contrast, DOC was observed to be highest (4.25mg Cl^–1) at the head of the inlet where pulpmill effluent was being discharged and a secondary maximum was found about 10km down-inlet from the dump site. The data suggest that a considerable proportion of the dredge spoil sinks rapidly near the dump site, probably within several hundred metres. Some of the spoil, perhaps low density wood debris may travel considerably further with the surface water where by leaching it may contribute to some extent to the surface DOC before sinking into deeper water.     

Spatial and temporal variation of particulate organic carbon in the PN section of East China Sea

1 IntroductionThe carbon cycle in the ocean, related to theglobal warming and human food, is of great scientificsignificance. Studies for the carbon transfer and trans-formation in the ocean, including the assimilative andmetabolic capacity, have become one of key researchfoci in global biogeochemical studies (Tsunogai et al.,1997; Hu and Yang, 2001; Hansell et al., 2003; Wei etal., 2003; Yang et al., 2004; Yuan et al., 2004).As is known, POC is composed of living fractionsand organic debr…     

Isotopic and biochemical composition of particulate organic matter in a shallow water estuary (Great Ouse, North Sea, England)

The biogeochemistry of particulate organic matter was studied in the Great Ouse estuary draining to the North Sea embayement known as the Wash from March 1990 to January 1991. Eleven locations were sampled monthly on a 50 km transect across the shallow estuary from the tidal weir to the middle of the Wash. Particulate organic carbon (POC) and total carbohydrate, protein and lipid analyses were combined with the determination of stable carbon isotopes. δ¹³C often increased from −30‰ in the river to −22‰ in the tidal freshwater reach. The mixing zone between fresh and marine tidal waters displayed only a slight increase in δ¹³C to −19‰. The change in δ¹³C values in the freshwater tidal reach demonstrated that mixing of riverborne and marine suspended POC was not the only process affecting the carbon stable isotope composition. Complementary sources, interfering considerably with the two end-member sources, may be identified as autocthonous primary production and resuspension of sediment that may be transported upstream. The respective importance of these sources is subject to seasonal variation. From March to August, high concentrations in carbohydrate and protein through the whole estuary indicate that despite turbidity significant primary production occurred. The proportional importance of the uncharacterized fraction of POC, which is considered as complex organic matter, was high from September to January and low from March to August. During most of the year, the biochemical compositions of particulate organic matter in the turbidity maximum and the rest of the estuary were similar. This contradicted the principle that owing to the long residence times of particles degradation processes largely dominate the production processes within the turbidity maximum. The occurence of significant in situ production in such shallow water estuaries may partially compensate for the degradation of suspended particulate organics, resulting in a complex relationship between the biogeochemical cycling and the fate of nutrients.     

Incorporation of aged dissolved organic carbon (DOC) by oceanic particulate organic carbon (POC): An experimental approach using natural carbon isotopes

Incorporation of ¹⁴C-depleted (old) dissolved organic carbon (DOC) on/into particulate organic carbon (POC) has been suggested as a possible mechanism to explain the low Δ¹⁴C-POC values observed in the deep ocean [Druffel, E.R.M., Williams, P.M., 1990. Identification of a deep marine source of particulate organic carbon using bomb ¹⁴C. Nature, 347, 172–174.]. A shipboard incubation experiment was performed in the Sargasso Sea to test this hypothesis. Finely ground dried plankton was incubated in seawater samples from the deep Sargasso Sea, both with and without a biological poison (HgCl₂). Changes in parameters such as biochemical composition and carbon isotopic signatures of bulk POC and its organic compound classes were examined to study the roles of sorptive processes and biotic activity on POC character. Following a 13-day incubation, the relative abundance of the acid-insoluble organic fraction increased. Abundances of extractable lipids and total hydrolyzable amino acids decreased for both treatments, but by a greater extent in the non-poisoned treatment. The Δ¹⁴C values of POC recovered from the non-poisoned treatment were significantly lower than the value of the unaltered plankton material used for the incubation, indicating incorporation of ¹⁴C-depleted carbon, most likely DOC. The old carbon was present only in the lipid and acid-insoluble fractions. These results are consistent with previous findings of old carbon dominating the same organic fractions of sinking POC from the deep Northeast Pacific [Hwang, J., Druffel, E.R.M., 2003. Lipid-like material as the source of the uncharacterized organic carbon in the ocean? Science, 299, 881–884.]. However, the Δ¹⁴C values of POC recovered from the poisoned treatment did not change as much as those from the non-poisoned treatment suggesting that biological processes were involved in the incorporation of DOC on/into POC.     

长江口盐度梯度下不同形态碳的分布、来源与混合行为

河口碳的生物地球化学过程是全球碳循环的重要组成。通过测定溶解无机碳（DIC）及其稳定同位素丰度（δ13C_DIC）,溶解有机碳（DOC）,有色溶解有机物（CDOM）,颗粒有机碳（POC）及其稳定同位素丰度（δ13C_POC）与元素比值（N/C）及相关指标,研究了2014年7月长江口盐度梯度下不同形态碳的分布、来源和混合行为。结果表明,DIC浓度、DOC浓度、POC含量分别为1 583.2~1 739.6 μmol/L,128.4~369.4 μmol/L和51.2~530.8 μmol/L,这些不同形态碳及CDOM的荧光组分的分布模式相似,均是从口内到口外,整体呈现先增大后减小的趋势,并与盐度呈现非保守混合行为。添加作用主要发生在在口门处最大浑浊带附近。与含量相反,从口内到口外,δ13C_DIC和δ13C_POC均呈现逐渐减小再增大的趋势,在口门附近达到最低值,分别为-9.7‰和-26.7‰。在口门附近不同形态碳含量上升及δ13C_DIC、δ13C_POC的降低可能主要与沉积物再悬浮及微生物作用有关。基于蒙特卡洛模拟的三端元混合模型的结果显示,河口内外POC来源变化明显,口内POC以陆源有机碳贡献为主,平均为62.3%,口外海源贡献逐渐增加。CDOM相关参数结果表明长江口CDOM主要来自陆源输入,海源及人类活动等也对其产生影响。     

春季长江口颗粒有机碳年际分布变化及其影响因素分析

根据2013—2016年春季(5月)长江口及其邻近海域4个航次环境综合调查数据,探讨春季长江口水体颗粒有机碳(POC)时空分布特征及其环境影响因素.结果显示:2013—2016年春季长江口POC浓度范围为0.22～16.99 mg/L,均值为1.80 mg/L,总水域POC年际间变化显著,底层浓度高于表层.从口门区、近...     

台湾海峡南部夏季的颗粒有机碳

根据2004年夏季、2005年夏季和2006年夏季3个航次观测的颗粒有机碳(POC)数据,表层POC含量的分布表现出近岸高、远岸低的特点,表层和次表层POC含量的高值区出现在东山以东以及南澳附近上升流区。沿岸流较强的2005年和2006年航次具有相对丰富的总悬浮颗粒物(TSM)含量。浮游植物是该区POC的主要来源。各航次的POC含量与叶绿素a(Chl a)含量正相关,所有航次统计的Chl a/POC与Chl a呈正相关,上升流区Chl a/POC偏小,上升流较强的航次高Chl a区的Chl a/POC也偏小,反映了上升流与高营养转换效率浮游生物生态在空间和时间上的联系。根据Chl a/POC~Chl a关系图判断,台湾海峡南部海域1988年、1998年和2004年夏季航次的浮游生物营养转换效率受到相对抑制,而在上升流信号较强的2005年和2006年夏季航次,上升流区的浮游生物高营养转换效率状态得以强化。各航次的POC含量和Chl a/POC比值与TSM含量正相关,POC/TSM比值与TSM负相关,沿岸流带来的陆源悬浮颗粒物通量波动,并没明显干扰台湾海峡南部以海洋浮游生物生态主导的颗粒有机碳生物地球化学循环格局。     

长江干流有机碳的时空输运特征及三峡工程对其影响

2006-04,2008-04,2008-05沿长江干流采集表层水样,并于2006-05~2007-05在下游大通站进行每月2次、为期1 a的连续观测,测定溶解有机碳(DOC)、颗粒有机碳(POC)及总悬浮物(TSM)。结果表明:长江重庆以上江段DOC浓度较低,重庆至河口由于人为污染排放DOC表现出高值;干流POC与TSM显著正先关,POC%(TSM)随TSM含量增大呈负指数关系下降。大通站有机碳浓度及通量均表现出明显的季节性,2006-06~2007-05全年经大通站进入河口的DOC、POC通量分别为1.17×106tC和1.88×106tC,其中洪季(5~10月)输运的有机碳占到总有机碳的70%,组成以颗粒态为主。三峡水库135 m及156 m蓄水后,泥沙在库区的沉降作用显著影响长江POC的输运特征及入海通量;从目前观测结果看,三峡库区DOC浓度并没有表现出明显的升高趋势,可能与水库运行时间尚短有关。     

Carbon Isotope Geochemistry of the Orinoco Basin

Stable carbon isotope ratios have been used to study the sources of particulate organic carbon (POC) and total dissolved inorganic carbon in the Orinoco Basin. The isotopic composition of total dissolved inorganic carbon shows a range of from -8·1 to -23·0 ppt, an indication of dominance of biological processes. The isotopic composition of POC exhibits a range of from -24·1 to -34·6 ppt with little seasonal variation. The isotopic evidence indicates that the POC is predominantly of terrestrial origin rather than a result of in situ planktonic production. The similarity of isotopic composition of POC and coastal sediments suggests that riverine organic detritus has been transported 30-50 km offshore in a direction parallel to the Orinoco river channel.     

Role of Zooplankton in the Vertical Mass Flux in the Kara and Laptev Seas in Fall

The role of zooplankton in the vertical mass flux in the Kara and Laptev seas was studied during cruise 63 of the R/V Akademik Mstislav Keldysh in August–October 2015. Mass fluxes were estimated using sediment trap samples. The maximum values of the total vertical flux (19600 mg m^?2 day^?1) and particulate organic carbon (POC) flux (464 mg C m^?2 day^?1) were measured close to the Lena River Delta in the Laptev Sea. In the Kara Sea, the total flux (80–2700 mg m^?2 day^?1) and the POC flux (17–130 mg C m^?2 day^?1) were substantially higher than the estimates published earlier. The fecal pellet flux varied from 2 to 92 mg C m^?2 day^?1 and made up 4–190% of the total organic carbon flux. The mineral composition of fecal pellets largely mirrored that of suspended particulate matter. Clay minerals in the fecal pellets were more abundant than in particulate matter in the areas with noticeable freshwater impact. The flux of zooplankton carcasses varied from 0.1 to 66.4 mg C m^?2 day^?1 and made up 0.2–72% of total POC flux. The results are discussed in relation to the abundance and composition of zooplankton, the concentration and composition of suspended particulate matter, hydrophysical conditions, and methods of sample preparation for analysis.     

Review and suggestions for estimating particulate organic carbon and dissolved organic carbon inventories in the ocean using remote sensing data

Dissolved organic carbon（DOC） and particulate organic carbon（POC） are basic variables for the ocean carbon cycle.Knowledge of the distribution and inventory of these variables is important for a better estimation and understanding of the global carbon cycle.Owing to its considerable advantages in spatial and temporal coverage,remote sensing data provide estimates of DOC and POC inventories,which are able to give a synthetic view for the distribution and transportation of carbon pools.To estimate organic carbon inventories using remote sensing involves integration of the surface concentration and vertical profile models,and the development of these models is critical to the accuracy of estimates.Hence,the distribution and control factors of DOC and POC in the ocean first are briefly summarized,and then studies of DOC and POC inventories and flux estimations are reviewed,most of which are based on field data and few of which consider the vertical distributions of POC or DOC.There is some research on the estimation of POC inventory by remote sensing,mainly in the open ocean,in which three kinds of vertical profile models have been proposed：the uniform,exponential decay,and Gauss models.However,research on remote-sensing estimation of the DOC inventory remains lacking.A synthetic review of approaches used to estimate the organic carbon inventories is offered and the future development of methods is discussed for such estimates using remote sensing data in coastal waters.     

南沙渚碧礁生态系有机碳的分布及周日变化特征

1999 年 4 月对我国南沙群岛渚碧礁海水中溶解有机碳的分布及礁坪区颗粒有机碳 (POC) 和溶解有机碳 (DOC) 的周日变化特征进行了观测。结果表明,渚碧礁表层海水 DOC 变化范围为 1.43~3.62 mg/L,平均为 2.16 mg/L,含量分布大致表现为礁坪区>潟湖>礁外。潟湖 DOC 的垂直分布大致表现为表层高于底层,可能与表层浮游植物的光合作用有关。礁坪区 POC 及 DOC 都呈现显著的周日变化特征,POC 呈现夜晚高,白天低的特点,浮游植物的昼夜垂直移动可能是产生该现象的主要原因。DOC 的周日变化则主要受浮游动物昼夜垂直移动及细菌等生物活动的影响。     

A new method of evaluating the mineralization of particulate and dissolved photoassimilated organic matter

A new method of evaluating the rate of mineralization of photoassimilated organic matter is described. This method enables us to compare the rate of direct mineralization of particulate organic carbon (POC) to CO₂ with the rate of solubilization of photoassimilated organic carbon followed by the mineralization of the resultant dissolved organic carbon (DOC) under the same conditions. The direct mineralization of photoassimilated carbon from POC to CO₂ is a more significant process compared with the mineralization of extracellular released organic carbon. The first-order rate coefficients range from 0.132 to 0.434 day^–1 for direct mineralization and 0.034 to 0.189 day^–1 for solubilization.     

东海颗粒有机碳的研究

于１９９４年春季（４月）和秋季（１０－１１月）对东海颗粒有机碳（ＰＯＣ），颗粒氮，ＡＴＰ（三磷酸腺苷）进行测定，通过ＡＴＰ定量区分ＰＯＣ中的生命与非生命部分，结果表明，春秋两季ＰＯＣ的平均值为４１７μｇ／Ｌ其中春季为２８０μｇ／Ｌ，生命部分占１０％；秋季为５４１μｇ／Ｌ，生命部分占４％，春季表层ＰＯＣ以东海陆架中部为高值区同周围递减，与ＡＴＰ的分布相似，而且颗粒有机物中的Ｃ：Ｎ比值较低（７．６３）     

Further investigations on why POC concentrations differ in samples collected by Niskin bottle and in situ pump

Particulate organic carbon (POC) concentrations measured in bottles are often higher than those measured by in situ pumps when samples are taken concurrently. In previous work, we suggested that differential collection of zooplankton might explain this systematic discrepancy in POC between these small volume (bottle) and large volume (in situ pump) techniques. We have now further quantified the carbon contributed by zooplankton collected in the >70-μm particulate fractions from both bottles and pumps at sites in the Mediterranean Sea and Long Island Sound. Our results show that zooplankton abundance and lipid concentrations from zooplankton are one order of magnitude higher in the bottles than in the pumps, supporting the idea that part of the pump–bottle difference is due to collection of more zooplankton by the bottles. Particle washout off the 70-μm mesh used in the in situ pump may cause loss of some particles as well. However, zooplankton in the >70-μm fraction from the bottles contributed only about 1–2 μM POC, which cannot explain the up to 20 μM POC differences observed in this study. Thus, the mechanisms leading to such a large POC difference are still unclear and need to be further investigated. POC concentrations measured using microquartz filters were similar to those using glass fiber filters, suggesting that filter types cannot explain the higher POC observed in bottles, where glass fiber filters are normally used. Furthermore, we investigated several different pump inlet designs to determine how these might affect the ability of pumps to collect and retain large (>70 μm) particles, including zooplankton. The comparison among different pump inlets suggests that inlet design affects the efficiency and retention of large particles and that a sealed filter holder with a narrow right-angle tubular opening is the most efficient at catching/retaining zooplankton.     

台湾海峡南部海域夏季上升流颗粒有机碳含量的逐日变化特征

根据2004—2006年夏季台湾海峡南部海域上升流区追踪过程中观测的颗粒有机碳（POC）、叶绿素o（ehl一0）、总悬浮颗粒物（TSM）含量数据,3个年份夏季上升流区POC含量范围分别为0．1150～0．2444、0．1391—0．6508、0．1068～0．5350m/dm^3,其平均值比同年份其他断面POC含量的平均值高．POC含量及Cchl-a／CPoc值的逐日变化对上升流事件的响应较好,反映出现场生产力对颗粒态有机碳的贡献与上升流发生过程的耦合;Cehl-a／CM值与chl一0含量呈正相关,在上升流的稳定期和衰减期,二者关系表现形式有所不同,能细分上升流事件的过程;上升流区的c洲一。／Ceo。值相对偏小,反映了上升流区浮游生物的高营养转换效率．POC和TSM含量的逐日变化关系在不同年份有不同表现,TSM含量对POC含量的影响存在促进和限制的可能;颗粒有机质含量占TSM比例的变化规律不明显,CPoc／CTsM值的逐日变化不能较好地响应上升流事件;CP0c／C鸭。值与TSM含量关系均呈负相关;受陆源有机物的补充及现场有机物的生物地球化学过程的影响,c眦／cTsM值与TSM含量关系更为复杂．     

Oxygen and organic carbon fluxes in sediments of the Bay of Biscay

The relationship between particulate organic carbon (POC) concentrations measured in modern sediment and fluxes of exported POC to the sediment surface needs to be understood in order to use POC content as a proxy of paleo-environmental conditions. The objective of our study was to compare POC concentrations, POC mineralization rates calculated from O₂ consumption and POC burial rates. Benthic O₂ distributions were determined in 58 fine-grained sediment cores collected at different periods at 14 stations in the southeastern part of the Bay of Biscay with depths ranging from 140 to 2800 m. Depth-dependent volume-specific oxygen consumption rates were used to assess rates of aerobic oxidation of organic matter (OM), assuming that O₂ consumption solely was related to heterotrophic activity at the sediment–water interface. Heterogeneity of benthic O₂ fluxes denoted changes in time and space of fresh organic material sedimentation. The most labile fraction of exported POC engendered a steep decrease in concentration in the upper 5 mm of vertical O₂ profiles. The rupture in the gradient of O₂ microprofile may be related to the bioturbation-induced mixing depth of fast-decaying carbon. Average diffusive O₂ fluxes showed that this fast-decaying OM flux was much higher than buried POC, although diffusive O₂ fluxes underestimated the total sediment oxygen demand, and thus the fast-decaying OM flux to the sediment surface. Sedimentary POC burial was calculated from sediment mass accumulation rate and the organic carbon content measured at the top of the sediment. The proportion of buried POC relative to total exported POC ranged at the most between 50% and 10%, depending on station location. Therefore, for a narrow geographic area like the Bay of Biscay, burial efficiency of POC was variable. A fraction of buried POC consisted of slow-decaying OM that was mineralized within the upper decimetres of sediment through oxic and anoxic processes. This fraction was deduced from the decrease with depth in POC concentration. At sites located below 500 m water depth, where the fast-decaying carbon did not reach the anoxic sediment, the slow-decaying pool may control the O₂ penetration depth. Only refractory organic material was fossilized in sedimentary records at locations where labile OM did not reach the anoxic portion of the sediment.     

Benthic community responses to pulses in pelagic food supply: North Pacific Subtropical Gyre

Time-series measurements of particulate organic carbon (POC) and particulate nitrogen (PN) fluxes, sediment community composition, and sediment community oxygen consumption (SCOC) were made at the Hawaii Ocean Time-series station (Sta. ALOHA, 4730 m depth) between December 1997 and January 1999. POC and PN fluxes, estimated from sediment trap collections made at 4000 m depth (730 m above bottom), peaked in late August and early September 1998. SCOC was measured in situ using a free vehicle grab respirometer that also recovered sediments for chemical and biological analyses on six cruises during the 1-year study. Surface sediment organic carbon, total nitrogen and phaeopigments significantly increased in September, corresponding to the pulses in particulate matter fluxes. Bacterial abundance in the surface sediment was highest in September with a subsurface high in November. Sediment macrofauna were numerically dominated by agglutinating Foraminifera fragments with highest density in September. Metazoan abundance, dominated by nematodes was also highest in September. SCOC significantly increased from a low in February to a high in September. POC and PN fluxes at 730 m above bottom were significantly correlated with SCOC with a lag time of ⩽14 days, linking pelagic food supply with benthic processes in the oligotrophic North Pacific gyre. The annual supply of POC into the abyss compared to the estimated annual demand by the sediment community (POC:SCOC) indicates that only 65% of the food demand is met by the supply of organic carbon.