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1.
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
2.
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
3.
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. 相似文献
4.
Water flows, concentrations of total (TOC), dissolved (DOC), and particulate (POC) organic carbon and seston were monitored for 52 diel periods in the single creek draining a 270-ha Spartina patens-Distichlis spicata marsh on the upper Texas coast. Rainfall, creek water flows, and water levels in the creek and on the marsh were measured by recording instruments.Rainfall accounted for most marsh flooding, and water outflow was significantly correlated with both rainfall and marsh water level. Creek flows were predominantly outward because microtopographic features and dense vegetation restricted overmarsh water flows and thereby reduced tidal flooding while extending the time of precipitation runoff. Concentrations of organic carbon in water leaving the marsh were highest in spring and summer and averaged 25·62, 21·41 and 3·35 mg l?1 of TOC, DOC and POC, respectively. These were 9·34, 9·93 and 0·04 mg l?1, respectively, higher than bay water. Most POC was 0·3–28 μm in diameter. Seston > 28μ leaving the marsh was 95% amorphous material; the rest was plankton, grass particles and fecal pellets. Loss of organic carbon was directly correlated with net water flux, and thus rainfall accounted for most carbon loss. Net carbon loss averaged 196 kg TOC, 150 kg DOC and 32 kg POC per day. Net annual loss was 2·4–5·5% of net aerial primary productivity (NAPP), or 21·55-30·09 g TOC m?2 year?1.Export from this marsh falls within the range found for other marshes and the data collectively indicate that coastal marshes are not losing as much organic carbon as has been suggested by indirect measurements. The discrepancy between potential and realized export is explained by the fact that export is not a simple removal of excess detritus by tidal action but is a more complicated process mediated by the interaction of additional factors such as rainfall, vegetation structure, microtopographic variation and decomposition, which can serve to reduce the amount and quality of NAPP exported. 相似文献
5.
东海中北部海域秋季表层海水中无机碳与海气界面碳的迁移 总被引：2，自引：0，他引：2
基于2010 年11 月对长江口外东海中北部海域的综合调查, 系统研究了该海域的无机碳体系参数的分布特征、海?气界面二氧化碳通量及其影响因素。研究结果表明, 该海域秋季溶解无机碳(DIC)高值区主要出现在调查海域东北部及长江口附近海域, 而调查海域南部DIC 含量较少且变化平缓, 其主要是受台湾东部流向东北方向的黑潮支流及长江冲淡水的影响; 表层海水CO2分压(pCO2)值变化范围为40.8～63.5 Pa, 呈现沿黑潮支流流入方向由东南向西北逐渐增高的趋势。秋季表层海水pCO2与温度(T)、盐度(S)有较好的负相关性, 说明海水温度升高和盐度增加, pCO2降低, 反之亦然。另外, 通过估算得出, 秋季CO2海-气交换通量为2.69～33.66 mmol/(m2·d), 平均值为(14.35 ± 7.06 )mmol/(m2·d),其在长江口邻近海域相对较大, 而在调查海域南部相对较小; 2010 年秋季水体向大气释放CO2的量(以碳计)为(2.35 ± 1.16)×104 t/d, 是大气CO2较强的源, 说明东海中北部海域秋季总体上是CO2的源。 相似文献
6.
2016年夏季黄、渤海颗粒有机碳的分布特征及影响因素 总被引：2，自引：1，他引：1
本文根据2016年6-7月黄、渤海航次获得的调查数据，分析了黄、渤海海域颗粒有机碳（POC）的浓度变化、空间分布特征并结合盐度、叶绿素a、POC/PON、POC/Chl a平面分布特征和相关性分析，探讨了黄、渤海海域POC的来源和影响因素。结果表明:2016年夏季渤海海域POC平均浓度（500.2±226.5）μg/L，北黄海POC平均浓度（358.2±101.5）μg/L，南黄海POC平均浓度（321.0±158.1）μg/L，渤海海域POC浓度高于黄海，整个海域POC浓度表层高于底层。POC的平面分布特征为近岸高，外海低。调查海域表层POC/PON均值为8.89，POC/Chl a均值为182.52；中层POC/PON均值为8.87，POC/Chl a均值为179.56；底层POC/PON均值为9.41，POC/Chl a均值为178.80。黄海海域浒苔衰败对POC/PON与POC/Chl a影响较大。相关性分析结果表明渤海海域盐度、总悬浮物和叶绿素a与POC存在显著的相关性，是影响POC分布的主要控制因素。南黄海除表层POC浓度与盐度、总悬浮物和叶绿素a浓度有很好的相关性外，中层和底层POC浓度与盐度、总悬浮物和叶绿素a浓度不存在显著的相关性。渤海海域POC主要受陆源和浮游植物共同影响，浮游植物是POC的主要贡献者，而黄海海域POC受长江冲淡水、黄海暖流、苏北沿岸流、生物活动和底层沉积物等多种因素影响，其中苏北近岸和青岛外海，有机碎屑为POC的主要贡献者。 相似文献
7.
基于2012年7月对东海的调查,剖析了其水体中各形态碳(pCO2、DIC、DOC、POC)的区域分布特征,估算了海-气界面CO2的交换通量(FCO2),探讨了影响其交换的主要因素,在此基础上,结合历史资料初步分析了近十几年来该海域海-气界面CO2交换通量的变化趋势。结果表明,2012年7月长江口邻近海域相对南部陆架区具有较低的DIC浓度,而DOC与POC的浓度相对较高。调查区域表层水pCO2变化范围为96.28~577.7μatm(1atm为101 325Pa),平均值为297.6μatm,低值区出现在长江冲淡水区(30°~33°N,123°~125°E),高值区主要分布在东海陆架的南部区域。表层水pCO2主要受控于长江冲淡水的输入和混合(盐度)、台湾暖流以及生物生产等。调查海域2012年7月海-气FCO2平均为(-6.410±7.486)mmol/(m2·d),表现东海在夏季是大气CO2的汇区,区域碳汇强度由强到弱依次为:长江冲淡水区(CDW)、黄东海混合水区(YEMW)、陆架咸淡水混合区(SMW)、近岸上升流区(CUW)和台湾暖流区(TWCW),东海夏季每日吸收大气CO2(以C计)约(18.3±19.8)kt。结合历史资料分析发现,近十几年来东海夏季碳汇强度有增强趋势,CDW区的海-气界面CO2通量平均年增速为-0.814mmol/(m2·d),即海水吸收大气二氧化碳每年增加约54.6kt,是夏季东海碳汇增加的最主要贡献者。 相似文献
8.
渤海春季浮游细菌分布与生态环境因子的关系 总被引：11，自引：2，他引：11
研究了 1 999年 4～ 5月渤海水体浮游细菌分布与生态环境因子的关系。结果显示 ,渤海春季表层水体浮游细菌含量与水温和溶解性有机碳呈正相关 ,相关系数分别为 0 .6 0 1 (P<0 .0 1 )和0 .4 0 6 (P<0 .0 5 ) ,并与溶解氧含量呈负相关 ,相关系数为 0 .5 1 9(P<0 .0 1 ) ;底层水体浮游细菌含量与水温、溶解性有机碳 (dissolved organic carbon,DOC)、颗粒性有机碳 (particulate organic carbon,POC)和叶绿素 a含量呈正相关 ,相关系数分别为 0 .82 0 (P<0 .0 1 ) ,0 .6 6 1 (P<0 .0 1 ) ,0 .5 31 (P<0 .0 1 )和 0 .4 42 (P<0 .0 5 ) ,并与溶解氧含量呈负相关 ,相关系数为 0 .6 5 0 (P<0 .0 1 )。表明水温和DOC、POC含量是渤海水域浮游细菌含量的主要限制因子 ,而水体中的溶解氧 (dissolved oxygen,DO)含量与浮游细菌的含量有关 相似文献
9.
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
10.
11.
渤海海峡冬季无机碳的立体分布特征及其源汇变化 总被引：1，自引：0，他引：1
根据2010年2月至2010年3月对渤海海峡3个断面39个站位表层、10 m层和30 m层水体中盐度、水温、叶绿素a以及无机碳等参数的测定数据,分析了该季节溶解无机碳的分布特征以及源汇变化状况,探讨了影响其分布的主要因素。结果显示,调查期间渤海海峡水体中各水层溶解无机碳(DIC)及其组分浓度分布较一致,其中DIC及HCO3-的浓度等值线分布均呈现出从西南向东北梯度降低的趋势,且受温度影响明显;二氧化碳分压[p(CO2)]则表现出与叶绿素a含量成明显负相关的分布特征;位于渤海海峡东部的H断面垂直方向上,由于受黄海、渤海水团在海峡中部交汇混合形成的水体紊流影响,DIC及其组分在断面中部等值线分布较两边曲折。冬季渤海海峡表现出明显的源、汇分区分布特征,整个调查区海-气二氧化碳通量为3.52 mmol/(m2·d),表现为大气CO2的弱源。冬季流经渤海海峡的DIC通量约为(130±2)×103 mol/s。 相似文献
12.
The likelihood that the carbon fluxes measured as part of the US-JGOFS field program in the equatorial Pacific ocean (EgPac) during 1992 yielded a balanced carbon budget for the surface ocean was determined. The major carbon fluxes incorporated into a surface carbon budget were: new production, particulate organic carbon (POC) and dissolved organic carbon (DOC) export, CaC03 export, C02 gas evasion, dissolved inorganic carbon (DIC) supply, and the time rate of charge. The ratio of the measured concentration gradients of DOC and DIC provided a constraint on the ratio of POC/DOC export. Uncertainties of ±30–50% for individual carbon flux measurements reduce the likelihood that a carbon balance can be measured during a JGOFS process-type study. As a benchmark, carbon fluxes were prescribed to yield a hypothetical surface carbon budget that was, on average, balanced. Given the typical errors in the individual carbon fluxes, however, there was only about a 30% chance that this hypothetical budget could be measured to be balanced to ±50%. Using this benchmark, it was determined that there was a 95 % chance that the carbon flux measurements yielded a surface DIC budget balanced (to ±50%) during El Nino conditions in boreal spring 1992, when the total organic carbon export rate was - 5 mmol C m-2 day- 1 and the POC export was 3 mmol C m−2 day−1. In boreal fall 1992, during cold period conditions, there was a 70% chance that the surface carbon DIC budget was balanced when the total organic carbon export rate was 20 mmol C m−2 day−1 and export was -13 mmol C m-2 day-'. The DOC to DIC concentration gradient ratio of - -0.15, measured in depth profiles down to 100m and in surface waters, was used as an important constraint that most (> 70%) of the organic carbon exported from the euphotic zone was POC rather than DOC. If a balanced surface DIC budget was used to test the compatibility of individual carbon fluxes measured during EgPac, then a three- to four-fold increase in total and particulate organic carbon export between spring and fall is indicated. This increase was not reflected in the POC loss rates measured by drifting sediment trap collections or estimated by234Th deficiencies coupled with the C/Th measured on suspended particles. 相似文献
13.
Abstract. A number of coastal organisms ( e.g ., bivalves) are known as important consumers of particulate organic carbon (POC) in the sea. In this paper we present new evidence that they are also important consumers of dissolved organic carbon (DOC) in the colloidal size range down to about 0.2 μm in diameter. Those colloids play an important role in the global flux of carbon in the seas.
We compare the uptake of colloidal DOC by marine bivalves of the North Sea and of the western Indian ocean.
To measure this uptake we made use of colloidal melanin as an alternative way to measure the uptake of colloidal DOC. 相似文献
We compare the uptake of colloidal DOC by marine bivalves of the North Sea and of the western Indian ocean.
To measure this uptake we made use of colloidal melanin as an alternative way to measure the uptake of colloidal DOC. 相似文献
14.
Caroline Kivimäe Richard G.J. Bellerby Agneta Fransson Marit Reigstad Truls Johannessen 《Deep Sea Research Part I: Oceanographic Research Papers》2010,57(12):1532-1542
The first carbon budget constructed for the Barents Sea to study the fluxes of carbon into, out of, and within the region is presented. The budget is based on modelled volume flows, measured dissolved inorganic carbon (DIC) concentration, and literature values for dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations. The results of the budget show that ～5600±660×106 t C yr?1 is exchanged through the boundaries of the Barents Sea. If a 40% uncertainty in the volume flows is included in the error calculation it resulted in a total uncertainty of ±1600×106 t C yr?1. The largest part of the total budget flux consists of DIC advection (～95% of the inflow and ～97% of the outflow). The other sources and sinks are, in order of importance, advection of organic carbon (DOC+POC; ～3% of both in- and outflow), total uptake of atmospheric CO2 (～1% of the inflow), river and land sources (～0.2% of the inflow), and burial of organic carbon in the sediments (～0.2% of the outflow). The Barents Sea is a net exporter of carbon to the Arctic Ocean; the net DIC export is ～2500±660×106 t C yr?1 of which ～1700±650×106 t C yr?1 (～70%) is in subsurface water masses and thus sequestered from the atmosphere. The net total organic carbon export to the Arctic Ocean is ～80±20×106 t C yr?1. Shelf pumping in the Barents Sea results in an uptake of ～22±11×106 t C yr?1 from the atmosphere which is exported out of the area in the dense modified Atlantic Waters. The main part of this carbon was channelled through export production (～16±10×106 t C yr?1). 相似文献
15.
黄、渤海沉积物中陆源脂类有机质的组成分布与转化特征 总被引：2，自引：0，他引：2
本文对黄、渤海表层沉积物中脂类化合物的组成进行了分析研究。结果表明,黄、渤海表层沉积物有机碳的含量为0.03%~1.02%,以黄河口含量最低,黄河口外和双台子河口外,以及北黄海和南黄海中部含量较高。有机质碳稳定同位素δ13C的分布为-21.55‰~-24.28‰,表征其陆海双重来源特征,并且海源特征由河口向海、由近岸向离岸逐渐增强。陆源脂类化合物以河口处略高,河道处略低,由河口向渤海中部和靠近渤海海峡方向迅速降低,表现出显著的河流输入特征;其形态组成由河道的游离态接近100%的绝对优势,迅速转变为渤海中部的以皂化结合态为主（大于50%）,仅在渤海中部和渤海海峡附近存在小于5%的矿物结合态,转化程度较低。北黄海中部和南黄海中部泥质区的有机碳和陆源脂类化合物显著富集,但其对总有机碳的相对贡献较小;其中皂化结合态超过50%,矿物结合态小于10%,说明其具有中等偏高的转化程度。 相似文献
16.
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
17.
海底地下水排放对典型红树林蓝碳收支的影响 总被引：1，自引：0，他引：1
海底地下水排放(Submarine Groundwater Discharge，SGD)是陆海相互作用的重要表现形式之一，其携带的物质对近岸海域生源要素的收支有重要影响。本文利用222Rn示踪技术估算了我国典型红树林海湾—广西珍珠湾在2019年枯季(1月)SGD携带的碳通量。调查发现，地下水中222Rn活度、溶解无机碳(DIC)和溶解有机碳(DOC)的平均浓度均高于河水和湾内表层海水。利用222Rn质量平衡模型估算得到珍珠湾SGD速率为(0.36±0.36) m/d，SGD输入到珍珠湾的DIC和DOC通量分别为(2.41±2.63)×107 mol/d和(1.96±2.20)×106 mol/d。珍珠湾溶解碳的源汇收支表明，SGD携带的DIC和DOC分别占珍珠湾总DIC和总DOC来源的91%和89%。因此，SGD携带的DIC和DOC是珍珠湾DIC和DOC的主要来源，是海岸带蓝碳收支和生物地球化学循环过程中的重要组成。 相似文献
18.
依据2017年8—9月对黄海海域溶解有机物(DOM)的调查，探讨了夏季黄海海水中溶解有机碳(DOC)和有色溶解有机物(CDOM)的空间分布特征。在表层海水中，受陆源影响较大的近岸海域CDOM含量相对较高，北黄海冷水团区域由于水产养殖的饵料引起DOC浓度升高，且该部分DOC以无色为主。DOC浓度随深度逐渐降低，而CDOM逐渐升高，该特征在冷水团区域更为显著，因此DOC和CDOM在冷水团区域的表底差异远大于浅水区的非冷水团区域。陆源输入和初级生产是引起表层DOC升高的主要原因，而光漂白则引起CDOM降低，同时光漂白还导致表层水体中CDOM分子量和芳香性低于底层。底层溶解氧饱和度在冷水团为80%～93%，均表现为弱不饱和状态。层化不仅阻碍了O2向底层水体输送，还抑制了DOC和CDOM的垂向混合，这是引起冷水团区域表底层DOC和CDOM差异较大的主要原因。 相似文献
19.
Photoreactivity of chromophoric dissolved organic matter transported by the Mackenzie River to the Beaufort Sea 总被引：3，自引：0，他引：3
The photoreactivity of chromophoric dissolved organic matter (CDOM) transported to Arctic shelf environments by rivers has only recently been studied and its quantitative role in Arctic shelf biogeochemistry has received little attention. Sunlight exposure experiments were performed on CDOM collected over a three year period (2002 to 2004) from river, estuary, shelf, and gulf regions of the Western Canadian Arctic. Decreases in CDOM absorption, synchronous fluorescence (SF), and dissolved organic carbon (DOC) concentration were followed after 3 days of exposure, and in two experiments, six optical cutoff filters were used to incrementally remove ultraviolet radiation incident on the samples. Apparent quantum yields for CDOM photobleaching (AQYble) and for DOC photomineralization (AQYmin) were computed, as were two AQY spectra (ble and min) for the Mackenzie River and a sample from the Mackenzie Shelf. The photoreactivity of Mackenzie River CDOM was highest after break-up and peak discharge and lowest in late summer. The half-lives of CDOM and DOC were estimated at 3.7 days and 4.8 days, respectively, when Mackenzie River water was exposed to full sunlight. Photobleaching of Mackenzie River CDOM fluorescence after most UV-B wavelengths were removed increased the correlation between the river and offshore waters in the Beaufort Sea. When light attenuation from particle- and CDOM-rich river water was considered for the Mackenzie Shelf, our photodegradation models estimated around 10% loss of absorption and < 1% DOC loss, suggesting that sunlight exposure does not substantially degrade CDOM on Arctic shelves. 相似文献
20.
渤海海峡冬季表层海水中溶解无机碳分布特征分析 总被引：1，自引：0，他引：1
根据2010 年2 月—2010 年3 月的调查数据, 探讨了冬季渤海海峡及其附近表层海水中溶解无机碳体系的分布特征。结果表明: 表层水体中TA、DIC 和HCO3- 的浓度分布总体上呈现出海峡西南部高东北部低的分布趋势。西南部出现的高值区, 与该区域靠近莱州湾, 受莱州湾水体污染影响有关。调查海域TA 与表层水的温度相关性明显, pH 与叶绿素的相关性较高。水温和Chl-a 浓度是影响水体中无机碳体系分布变化的重要因素。其中, 水温对HCO3- 的影响要明显强于DIC。海峡南北两侧水体交换的差异, 是导致海峡南部东西两端无机碳体系各参数监测数值的差异明显大于海峡北部的主要原因。 相似文献