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1.
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. 相似文献
2.
黄河干流有机碳的时空分布特征 总被引：4，自引：0，他引：4
通过2003-2009年多个航次对黄河干流DOC(溶解有机碳)和POC(颗粒有机碳))及相关参数的调查研究,结果表明:TSS(颗粒悬浮物)为91.42～8188 mg/L,POC为0.65～24.20 mg/L,POC%(POC/TSS×100%)为0.44%～2.21%,DOC为1.57～4.77 mg/L,有机碳沿程分布具有明显的空间特征.花园口水文年调查中有机碳含量与流量的季节变化密切相关.POC主要受冲刷影响,而DOC在不同季节分别体现出冲刷、稀释或浓缩效应.修建水库和调水调沙这2个显著的人为干扰活动对黄河有机碳的性质及输运产生了截然不同的影响:库区自生源对有机碳的贡献明显大于干流,DOC/POC为6.64～12.00,DOC是有机碳的主要形式,同时水库截流,颗粒物沉降降低了颗粒有机碳的输运量,而调水调沙却加强了有机碳的输运,该时期DOC/POC为0.01～0.47,POC是有机碳输运的主导形态. 相似文献
3.
2006年12月在海南省东北部河流万泉河和文昌河以及周边的红树林和珊瑚礁体系采集水样,测定其溶解有机碳(DOC)和颗粒有机碳(POC)的含量.结果表明,万泉河水体中DOC和POC的平均浓度分别为139.3和39.7μmol·L-1;文昌河水体中DOC和POC的平均浓度则为133.0和47.4μmol·L-1,其周边红树林水体DOC和POC的平均浓度分别为214.1和27.9μmol·L-1;珊瑚礁周边水体DOC和POC的平均浓度分别为66.3和22.41μmol·L-1.文昌河周边的养殖活动及红树林水体对该河流中的高DOC和POC可能有显著贡献,且文昌河POC%与TSM浓度均呈显著负相关(R2=0.71,n=9).万泉河、文昌河和珊瑚礁周边水体POC/Chl a的比值分别介于72-312、43-196、122.5-334.估算浮游植物对万泉河、文昌河和珊瑚礁周边水体POC的贡献量分别为34%、45%、38%. 相似文献
4.
双台子河口水体有机碳分布特征研究 总被引：1，自引：0，他引：1
于2011年5月和8月通过研究双台子河口水体溶解有机碳(DOC)、颗粒有机碳(POC)和化学耗氧量(COD)的分布特征,阐述双台子河口水体有机碳的河口过程及其影响因素,并探讨总有机碳(TOC)和COD表征河口有机污染的区域性和季节性特征。研究表明:2011年5月双台子河口DOC、POC和COD含量范围分别为4.04~5.06mg/L(平均4.60mg/L)、2.93~10.85mg/L(平均7.01mg/L)和5.65~14.07mg/L(平均9.04mg/L);8月分别为10.87~46.04mg/L(平均26.75mg/L)、0.88~17.27mg/L(平均4.16mg/L)和2.42~67.62mg/L(平均17.85mg/L)。DOC、POC和COD的含量由河到海总体呈现逐渐降低的趋势,双台子河口不同区段DOC、POC和COD的时空分布,及其主要和次要影响因素具有一定的差别。有机碳来源和海水的稀释作用是影响双台子河口有机碳分布的主要因素,现场生物生产和悬浮颗粒物影响较小。双台子河口水体中TOC和COD呈现线性不显著正相关关系,二者关系的季节差异显著。 相似文献
5.
6.
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。 相似文献
7.
南沙渚碧礁生态系有机碳的分布及周日变化特征 总被引：4，自引：0，他引：4
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。 相似文献
8.
《中国海洋大学学报(自然科学版)》2020,(Z1)
河流是连接陆地和海洋两大碳库的重要通道,正确认识不同水文条件下河流碳输运规律是全球碳循环研究的重要方面。本文于2017年每月在黄河利津浮桥采集水样和颗粒物样品,通过分析溶解有机碳(Dissolved organic carbon, DOC)、颗粒有机碳(Particulate organic carbon, POC)及其稳定同位素(δ~(13)C-POC),结合流量、悬浮颗粒物(Suspended particulate matter, SPM)、温度、pH和溶解氧(Dissolved oxygen, DO)等水文参数讨论了黄河在此特枯年入海有机碳的季节变化规律及其影响因素,并对有机碳的入海通量进行了估算。结果表明,2017年利津的流量和SPM含量明显低于以往年份,年均分别为(262±144) m~3/s和(126.8±79.9) mg/L。DOC的年均浓度为(3.06±0.95) mg/L,夏季最高,其它季节变化不显著。POC(%)(1%代表0.01 g/gdw (g dry sediment))的年平均值为(2.12±1.85)%,夏秋季节较高,高值出现在7、8和9月份。POC浓度的年平均值为(2.23±1.43) mg/L。颗粒物的δ~(13)C和C/N范围分别为-26.9‰～-25.1‰和3.2～12.5,表明2017年利津POC可能主要来源于黄河流域土壤和淡水浮游植物。2017年DOC和POC的入海通量(以C计)分别为2.8×10~(10)和1.3×10~(11 )g,两者均表现为夏秋季节较高。年入海有机碳通量之比,即DOC/POC(g/a/g/a)为0.22,这一数值高于以往年份,说明2017年黄河入海的有机碳中溶解态有机碳所占比例有增大趋势。在人类活动和气候变化的双重影响下,黄河水沙通量持续降低,近些年来甚至达到特枯状态,其对黄河碳输运及河口、边缘海生物地球化学的深远影响需要引起高度重视和关注。 相似文献
9.
三峡截流后长江口秋季TSM、POC和PN的分布特征 总被引：2，自引：0，他引：2
基于2004年11—12月长江口56个站位的悬浮体调查资料,分析了长江口区悬浮体总量(TSM)、颗粒有机碳(POC)和颗粒氮(PN)质量浓度的平面分布特征,探讨该区TSM及颗粒有机质的物质来源和三峡截流对长江三角洲的影响。结果表明,表、底层TSM与POC、PN质量浓度之间存在显著的正线性相关关系并都呈现出南高北低的格局,说明了长江悬浮颗粒物入海后主要沿东南方向输运。POC、PN质量分数与POC、PN的质量浓度不同,它们与TSM质量浓度对数有负相关关系。由于河口区底质再悬浮作用显著,TSM和POC、PN质量浓度呈现表层低、底层高的特点。长江口悬浮体主要来自长江径流和底质沉积物的再悬浮。与三峡截流前数据的对比表明,截流对目前长江口区的TSM和POC尚未造成明显的影响。 相似文献
10.
2012年长江口水域溶解有机碳分布特征及其与环境因子的关系 总被引：1，自引：0，他引：1
根据2012年2、5、8和11月长江口4个季节航次综合调查资料,分析了长江口及其邻近海域溶解有机碳(DOC)时空分布特征,探讨了DOC分布与盐度、表观耗氧量(AOU)、化学耗氧量(COD)、叶绿素a以及颗粒有机碳(POC)间的关系。结果表明,2012年长江口区DOC的浓度范围在0.53~5.21mg/L之间,均值为1.86mg/L。DOC浓度秋季最高,夏季和冬季次之,春季最低。DOC空间分布整体呈现近岸高、远岸低的格局,高值区分布在口门内和近岸水域,外海区DOC浓度随着离岸距离的增加而逐渐降低。各季节DOC空间分布略有差异。DOC与盐度、COD以及POC的相关关系较强,与AOU和叶绿素a相关性较弱。2012年长江口有机碳以DOC为主,DOC对总有机碳(TOC)的平均贡献率为55.8%,其中冬季贡献最大(59.4%),其次为秋季(59.2%)和春季(55.3%),夏季贡献率最低(49.4%)。 相似文献
11.
Amelia De Lazzari Daniela Berto Daniele Cassin Alfredo Boldrin Michele Giani 《Marine Ecology》2008,29(4):469-482
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. 相似文献
12.
Dissolved organic carbon (DOC), stable carbon isotopic (δ13C) compositions of DOC and particulate organic carbon (POC), and elemental C/N ratios of POC were measured for samples collected from the lower Mississippi and Atchafalaya rivers and adjacent coastal waters in the northern Gulf of Mexico during the low flow season in June 2000 and high flow season in April 2001. These isotopic and C/N results combined with DOC measurements were used to assess the sources and transport of terrestrial organic matter from the Mississippi and Atchafalaya rivers to the coastal region in the northern Gulf of Mexico. δ13C values of both POC (−23.8‰ to −26.8‰) and DOC (−25.0‰ to −29.0‰) carried by the two rivers were more depleted than the values measured for the samples collected in the offshore waters. Strong seasonal variations in δ13C distributions were observed for both POC and DOC in the surface waters of the region. Fresh water discharge and horizontal mixing played important roles in the distribution and transport of terrestrial POC and DOC offshore. Our results indicate that both POC and DOC exhibited non-conservative behavior during the mixing especially in the mid-salinity range. Based on a simple two end-member mixing model, the comparison of the measured DOC-δ13C with the calculated conservative isotopic mixing curve indicated that there was a significant in situ production of marine-derived DOC in the mid- to high-salinity waters consistent with our in situ chlorophyll-a measurements. Our DOC-δ13C data suggest that a removal of terrestrial DOC mainly occurred in the high-salinity (>25) waters during the mixing. Our study indicates that the mid- to high- (10–30) salinity range was the most dynamic zone for organic carbon transport and cycling in the Mississippi River estuary. Variability in isotopic and elemental compositions along with variability in DOC and POC concentrations suggest that autochthonous production, bacterial utilization, and photo-oxidation could all play important roles in regulating and removing terrestrial DOC in the northern Gulf of Mexico and further study of these individual processes is warranted. 相似文献
13.
长江口盐度梯度下不同形态碳的分布、来源与混合行为 总被引：1，自引：0，他引：1
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（δ13CDIC），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（δ13CPOC）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，δ13CDIC和δ13CPOC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δ13CDIC、δ13CPOC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。 相似文献
14.
Review and suggestions for estimating particulate organic carbon and dissolved organic carbon inventories in the ocean using remote sensing data 总被引：2，自引：0，他引：2
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. 相似文献
15.
Sarah A. Bennett Peter J. StathamDarryl R.H. Green Nadine Le BrisJill M. McDermott Florencia PradoOlivier J. Rouxel Karen Von Damm Christopher R. German 《Deep Sea Research Part I: Oceanographic Research Papers》2011,58(9):922-931
Chemoautotrophic production in seafloor hydrothermal systems has the potential to provide an important source of organic carbon that is exported to the surrounding deep-ocean. While hydrothermal plumes may export carbon, entrained from chimney walls and biologically rich diffuse flow areas, away from sites of venting they also have the potential to provide an environment for in-situ carbon fixation. In this study, we have followed the fate of dissolved and particulate organic carbon (DOC and POC) as it is dispersed through and settles beneath a hydrothermal plume system at 9°50′N on the East Pacific Rise. Concentrations of both DOC and POC are elevated in buoyant plume samples that were collected directly above sites of active venting using both DSV Alvin and a CTD-rosette. Similar levels of POC enrichment are also observed in the dispersing non-buoyant plume, ∼500 m downstream from the vent-site. Further, sediment-trap samples collected beneath the same dispersing plume system, show evidence for a close coupling between organic carbon and Fe oxyhydroxide fluxes. We propose, therefore, a process that concentrates POC into hydrothermal plumes as they disperse through the deep-ocean. This is most probably the result of some combination of preferential adsorption of organic carbon onto Fe-oxyhydroxides and/or microbial activity that preferentially concentrates organic carbon in association with Fe-oxyhydroxides (e.g. through the microbial oxidation of Fe(II) and Fe sulfides). This potential for biological production and consumption within hydrothermal plumes highlights the importance of a multidisciplinary approach to understanding the role of the carbon cycle in deep-sea hydrothermal systems as well as the role that hydrothermal systems may play in regulating global deep-ocean carbon budgets. 相似文献
16.
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 总被引：1，自引：0，他引：1
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． 相似文献