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1.
根据2012年9月在黄河口及莱州湾取得的悬浮体和水文调查资料,探讨了非调水调沙期间黄河15及莱州湾颗粒有机碳(POC)的地球化学特征及其影响因素。结果表明:(1)2012年秋季黄河口及莱州湾POC浓度介于42.25-1018.87gg/L之间,平均为316.35μg/L,底层POC浓度高于表层,这与沉积物再悬浮有直接关系;(2)黄河口POC呈现近岸区高,远岸区低的趋势,高值区出现在新、老两个河口区域,指示了陆源输入对河口区POC的直接控制作用;(3)在盐度为26~28(psu)之间黄河口POC有高值,表明絮凝沉降作用对POC空间分布的影响;底层POC与浊度显著相关,表明海底沉积物再悬浮对研究区POC空间分布的直接影响;悬浮物含量超过20mg/L时,生命态颗粒有机碳对总颗粒有机碳的贡献明显下降;(4)POC/PN值显示黄河15及莱州湾POC来源的复杂性,生物作用、沉积物再悬浮和黄河水沙输入对研究区的POC生物地球化学过程都有一定的影响。  相似文献   

2.
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。  相似文献   

3.
许斐  杨守业  展望  李超  钱鹏 《地球化学》2011,40(2):199-208
2008年4月至2009年4月,在南通长江干流每周采集一次表层悬浮物样品,共51个,分析了其粒度、颗粒有机碳(POC)、颗粒氮(PN)含量以及有机碳同位素(δ13Corg)组成,研究了下游干流颗粒有机碳组成的季节性变化特征.悬浮物的平均粒径在一年内变化不明显,而POC和PN含量呈现洪季缓慢减小,枯季增加的趋势;δ13C...  相似文献   

4.
乌裕尔河流域颗粒有机碳的来源:碳同位素证据   总被引:1,自引:0,他引:1       下载免费PDF全文
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...  相似文献   

5.
青岛邻近海域海水中有机碳的分布特征   总被引:1,自引:0,他引:1  
在2006年8月、12月和2007年4月、10月对青岛邻近海域进行了4个季节的调查,分析了溶解有机碳(DOC)和颗粒有机碳(POC)的分布特征及影响因素.结果表明,调查海区DOC的浓度范围为1.23-3.15 mg/L,年平均值为1.70 mg/L,POC的浓度范围为0.09-1.04 mg/L,年平均值为0.28 m...  相似文献   

6.
西江流域的有机碳侵蚀通量   总被引:12,自引:1,他引:11  
在西江下游的马口水文站对径流进行了4个季节的有机碳采样分析。研究表明,西江径流有机碳的断面构成在各个季节均较为一致;季节性变化表现为,有机碳和悬浮物含量随流量的增加而增加。随着水体悬浮物含量的增加,悬浮物的有机碳含量呈对数趋势降低。西江流域的有机碳侵蚀通量为10.18×106gC/km2·yr.,是全球外流域有机碳侵蚀通量的2~3倍,其中以颗粒有机碳的侵蚀通量为主,达到8.30×106gC/km2·yr.,溶解有机碳的侵蚀通量为1.88×106gC/km2·yr.。反映了流域内较强的机械剥蚀过程,这与西江流域典型的季风气候、较大的地形高差,以及农业耕作历史长久、土地利用强度较大等因素有关。  相似文献   

7.
黄渤海有机碳的分布特征及收支评估研究   总被引:4,自引:1,他引:3  
陆架边缘海是陆海相互作用研究中最为关键的区域,也是全球重要的碳储库,在区域物质循环过程中发挥着重要的作用。基于2012年5月和11月对黄渤海海域的综合调查,对该海域水体和沉积物中有机碳的含量与分布进行了分析,并结合相关文献资料对黄渤海有机碳的收支进行了估算。主要结论为:黄渤海溶解有机碳和颗粒有机碳均呈近岸河口区域高、离岸低的分布趋势;有机碳的组成以溶解有机碳为主,颗粒有机碳由海洋自生的有机碳和陆地来源的有机碳组成;黄渤海沉积物有机碳高值区主要分布在河口和泥质区,其组成也是由海洋自生和陆源混合而成,其中渤海以陆源为主,而黄海以海源为主。黄渤海有机碳收支评估表明,有机碳的主要来源为初级生产力产生的有机物,其贡献为(6 760±971)×104t/a,占有机碳输入总量的(74±10)%,沉积物再悬浮的通量为(884±200)×104t/a,东海向黄海输入的通量为(679±107)×104t/a,河流及陆源输入的通量为(643±63)×104t/a,大气干湿沉降的通量为(141±39)×104t/a,其贡献分别占有机碳输入总量的(10±2.2)%,(7.5±1.2)%,(7.0±0.7)%和(1.5±0.4)%;黄渤海有机碳的主要支出为呼吸消耗,其贡献为(5 190±746)×104t/a,占有机碳输出总量的(57±8.2)%,黄海向东海输出的通量为(2 150±370)×104t/a,有机碳沉积通量为(1 030±225)×104t/a,有机碳降解通量为(737±191)×104t/a,其贡献分别占有机碳输出总量的(24±4.1)%,(11±2.5)%和(8.0±2.1)%。有机碳收支评估表明黄渤海有机碳以海洋自生来源为主,且具有潜在碳的"汇"的特性,水体中外源输入和海洋自生有机碳的(1.6±0.3)%埋藏于该海域内。  相似文献   

8.
增江颗粒有机碳同位素的AMS研究初报   总被引:3,自引:0,他引:3  
全球河流每年向海洋输送约1Gt(1015g)的碳,其中40%为有机碳。然而,在海洋沉积物中却难以寻找到足量的陆地碳的生物地球化学标记[1]。显然,陆地碳在河流搬运过程中经历了复杂的生物地球化学变化,乃至“踪迹全无”。河流有机碳可大体上划分为颗粒态(POC)和溶解态(DOC)两种基本类型。就全球范围讲,河流输送的POC和DOC在数量上相当或DOC略高些。但在一些高浑浊的河流,尤其是亚洲季风区的河流中,POC在有机碳中却占绝对优势。如珠江干流水体中POCDOC比值高达5.0左右[2]。因此,亚洲季风区河流中所搬运的POC对其注入水域的生物地球化学过程影响深远。河流有机质的来源复  相似文献   

9.
珠江马口站,河口站断面水体有机碳含量的季节变化   总被引:15,自引:2,他引:13  
高全洲  沈承德 《地球化学》1999,28(3):273-280
1997年7月份和11月份对北河口站和西江马口站水体有机碳含量进行了两次采样分析。结果表明;两江水体的颗粒有机碳含量在不同 均高于溶解有机碳含量,这与全球河流以溶解有机碳为主的平均格局显著不同。溶解有机碳,颗粒有机碳含量以及总有机碳含量均不文季节的变化而变化,汛期含量高于平水期。悬浮物中有机碳的含量的随悬浮物含量的增加,也即流域土壤机械侵蚀强度的加强而降低,这种现象与全球河流的总体趋势一致。汛期水  相似文献   

10.
文章以耕地为对照,分析不同石漠化治理措施(花椒林和次生林)对土壤0~20 cm土层有机碳(SOC)、颗粒有机碳(POC)、矿物结合有机碳(MOC)和团聚体有机碳的影响,探讨POC、MOC与SOC、团聚体有机碳的关系。结果表明:与耕地相比,花椒林和次生林均不同程度提高SOC、POC、MOC和团聚体有机碳含量。0~10 cm土层次生林SOC含量和各粒径团聚体有机碳含量均显著高于耕地和花椒林,在10~20 cm土层无显著差异;0~20 cm土层花椒林和次生林土壤POC含量显著高于耕地,MOC无显著差异。POC/SOC范围为20.38%~45.27%,花椒林和次生林显著高于耕地。相反,MOC/SOC为耕地显著高于花椒林和次生林 。退耕为花椒林和次生林后,SOC含量的增加主要以POC含量增加为主。次生林和花椒林>2 mm粒径对SOC贡献率显著高于耕地,但0.25~2 mm粒径、0.053~0.25 mm粒径和 < 0.053 mm粒径对SOC贡献率显著低于耕地。其相关分析表明:POC、MOC与SOC、团聚体有机碳的关系均呈正相关,表现为次生林 > 花椒林 > 耕地。退耕恢复为花椒林和次生林后,SOC、POC和MOC增加量与团聚体有机碳增加量显著相关,其以次生林的相关性较强。石漠化治理措施改变SOC物理组分及其组成以及它们之间的关系,从而促进有机碳的积累。   相似文献   

11.
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.  相似文献   

12.
Global riverine carbon concentrations and fluxes have been impacted by climate and human-induced changes for many decades. This paper aims to reconstruct the longterm carbon concentrations and carbon fluxes of the Red River, a system under the coupled pressures of environmental change and human activity. Based on (1) the relationships between particulate and dissolved organic carbon (POC, DOC) or dissolved inorganic carbon (DIC), and suspended sediments (TSS) or river water discharge and on (2) the available detailed historical records of river discharge and TSS concentration, the variations of the Red River carbon concentration and flux were estimated for the period 1960–2015. The results show that total carbon flux of the Red River averaged 2555?±?639 kton C year?1. DIC fluxes dominated total carbon fluxes, representing 64% of total, reflecting a strong weathering process from carbonate rocks in the upstream basin. Total carbon fluxes significantly decreased from 2816 kton C year?1 during the 1960s to 1372 kton C year?1 during the 2010s and showed clear seasonal and spatial variations. Organic carbon flux decreased in both quantity and proportion of the total carbon flux from 40.9% in 1960s to 14.9% in 2010s, reflecting the important impact of dam impoundment. DIC flux was also reduced over this period potentially as a consequence of carbonate precipitation in the irrigated, agricultural land and the reduction of the Red River water discharge toward the sea. These decreases in TSS and carbon fluxes are probably partially responsible for different negatives impacts observed in the coastal zone.  相似文献   

13.
Arctic rivers typically transport more than half of their annual amounts of water and suspended sediments during spring floods. In this study, the Sagavanirktok, Kuparuk and Colville rivers in the Alaskan Arctic were sampled during the spring floods of 2001 to determine levels of total suspended solids (TSS) and dissolved and particulate metals and organic carbon. Concentrations of dissolved organic carbon (DOC) increased from 167 to 742 μmol/L during peak discharge in the Sagavanirktok River, at about the same time that river flow increased to maximum levels. Concentrations of dissolved Cu, Pb, Zn and Fe in the Sagavanirktok River followed trends observed for DOC with 3- to 25-fold higher levels at peak flow than during off-peak discharge. Similar patterns were found for the Kuparuk and Colville rivers, where average concentrations of dissolved trace metals and DOC were even higher. These observations are linked to a large pulse of DOC and dissolved metals incorporated into snowmelt from thawing ponds and upper soil layers. In contrast with Cu, Fe, Pb and Zn, concentrations of dissolved Ba did not increase in response to increased discharge of water, TSS and DOC. Concentrations of particulate Cu, Fe, Pb and Zn were more uniform than observed for their respective dissolved species and correlated well with the Al content of the suspended particles. However, concentrations of particulate Al were poorly correlated with particulate organic carbon. Results from this study show that >80% of the suspended sediment and more than one-third of the annual inputs of dissolved Cu, Fe, Pb, Zn and DOC were carried to the coastal Beaufort Sea in 3 and 12 d, respectively, by the Kuparuk and Sagavanirktok rivers.  相似文献   

14.
The delivery of organic carbon (C) from rivers to the coastal ocean via estuaries is recognized as an important component of the global C budget however, smaller river systems are often overlooked and modern flux estimates are not very different from historical estimates. Here, the seasonal (wet vs. dry) concentration and fluxes of dissolved organic C (DOC) were measured in five small sub-tropical rivers that drain into the Tampa Bay (FL, USA) estuary. DOC distributions were highly variable among riverine, mesohaline, and marine end-member samples in all river catchments and no significant differences were observed among or between DOC concentrations with respect to river catchment, season, or year of sampling. In general, DOC mixed non-conservatively during the wet seasons, and conservatively during the dry seasons, with the estuarine reaches of each river serving as a sink of DOC. Fluxes were strongly tied to discharge irrespective of season, and the estuaries removed 15–65% of DOC prior to export to coastal Bay and Gulf of Mexico waters. DOC concentrations were similar to others reported for low-elevation sub-tropical rivers, and a combination of elevation, residence time, and climate appear to control the abundance and variability of DOC in sub-tropical vs. tropical river systems. The characterization of DOC in small, sub-tropical rivers, which share characteristics with both their temperate and tropical counterparts, is critical for quantitatively constraining the importance of these systems in local-to-regional scale ocean C budgets. In addition to geomorphic properties, the role of past, present, and future land cover and other environmental change in small coastal rivers also exerts control on the quantity and flux of DOC in these systems.  相似文献   

15.
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.  相似文献   

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