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1.
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
2.
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
3.
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
4.
Absorption and fluorescence of chromophoric dissolved organic matter (CDOM) and dissolved organic carbon (DOC) measurements were performed during three oceanographic surveys in 1994 in the southern Baltic Sea (Polish area of the Baltic Proper). DOC was measured both by high-temperature catalytic oxidation (HTCO) and low-temperature oxidation (LTO) conventional persulphate methods. CDOM fluorescence was shown to be highly correlated with absorption, with the same regression parameters, despite the seasonal change in different hydrographic conditions and the fluorescence quantum yield variations (1.23 ± 0.07 in April and 0.97 ± 0.12 in September). The results show a good correlation between the optical parameters and DOC although ˜ 70% of the DOC does not display significant absorption in the UV-visible range (350–750 nm). The non-absorbing DOC measured with HTCO method appears unaffected by seasonal changes. Consequently, total DOC can be predicted by optical methods using remote sensing techniques. The non-absorbing DOC measured by LTO method varies from 62% (April) to 76% (September), which implies that there is requirement for estimates on a seasonal basis. 相似文献
5.
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
6.
Robert Turnewitsch Barbara M. Springer Konstadinos Kiriakoulakis Juan Carlos Vilas Javier Arístegui George Wolff Florian Peine Stephan Werk Gerhard Graf Joanna J. Waniek 《Marine Chemistry》2007,105(3-4):208-228
Particulate matter in aquatic systems is an important vehicle for the transport of particulate organic carbon (POC). Its accurate measurement is of central importance for the understanding of marine carbon cycling. Previous work has shown that GF/F-filter-based bottle-sample-derived concentration estimates of POC are generally close to or higher than large-volume in-situ-pump-derived values (and in some rare cases in subzero waters are up to two orders of magnitude higher). To further investigate this phenomenon, water samples from the surface and mid-water Northeast Atlantic and the Baltic Sea were analyzed. Our data support a bias of POC concentration estimates caused by adsorption of nitrogen-rich dissolved organic material onto GF/F filters. For surface-ocean samples the mass per unit area of exposed filter and composition of adsorbed material depended on the filtered volume. Amounts of adsorbed OC were enhanced in the surface ocean (typically 0.5 μmol cm− 2 of exposed filter) as compared to the deep ocean (typically 0.2 μmol cm− 2 of exposed filter). These dependencies should be taken into account for future POC methodologies. Bottle/pump differences of samples that were not corrected for adsorption were higher in the deep ocean than in the surface ocean. This discrepancy increased in summer. It is shown that POC concentration estimates that were not corrected for adsorption depend not only on the filtered volume, true POC concentration and mass of adsorbed OC, but also on the filter area. However, in all cases we studied, correction for adsorption was important, but not sufficient, to explain bottle/pump differences. Artificial formation of filterable particles and/or processes leading to filterable material being lost from and/or missed by sample-processing procedures must be considered. It can be deduced that the maximum amounts of POC and particulate organic nitrogen (PON) that can be artificially formed per liter of filtered ocean water are 3–4 μM OC (5–10% of dissolved OC) and 0.2–0.5 μM ON (2–10% of dissolved ON), respectively. The relative sensitivities of bottle and pump procedures, and of surface- and deep-ocean material, to artificial particle formation and the missing/losing of material are evaluated. As present procedures do not exist to correct for all possible biasing effects due to artificial particle formation and/or miss/loss of filterable material, uncertainties of filtration-based estimates of POC concentrations need further testing. The challenge now is to further constrain the magnitude of the biasing effects that add to the adsorption effect to reduce the uncertainties of estimates of POC concentrations, inventories and fluxes in the ocean. 相似文献
7.
C.B. Lopes A.I. Lilleb P. Pato J.M. Dias S.M. Rodrigues E. Pereira A.C. Duarte 《Estuarine, Coastal and Shelf Science》2008,79(4):751-757
Land/ocean boundaries constitute complex systems with active physical and biogeochemical processes that affect the global carbon cycle. An example of such a system is the mesotidal lagoon named Ria de Aveiro (Portugal, 40°38′N, 08°45′W), which is connected to the Atlantic Ocean by a single channel, 350 m wide. The objective of this study was to estimate the seasonal and inter-tidal variability of organic carbon fluxes between the coastal lagoon and the Ocean, and to assess the contribution of the organic carbon fractions (i.e. dissolved organic carbon (DOC) and particulate organic carbon (POC)) to the export of organic carbon to the Ria de Aveiro plume zone. The organic carbon fractions fluxes were estimated as the product of the appropriate fractional organic carbon concentrations and the water fluxes calculated by a two-dimensional vertically integrated hydrodynamic model (2DH). Results showed that the higher exchanges of DOC and POC fractions at the system cross-section occurred during spring tides but only resulted in a net export of organic carbon in winter, totalling 85 t per tidal cycle. Derived from the winter and summer campaigns, the annual carbon mass balance estimated corresponded to a net export of organic carbon (7957 = 6585 t yr−1 POC + 1372 t yr−1 DOC). On the basis of the spring tidal drainage area, it corresponds to an annual flux of 79 g m−2 of POC and 17 g m−2 of DOC out of the estuary. 相似文献
8.
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
9.
Malgorzata Stramska 《Deep Sea Research Part I: Oceanographic Research Papers》2009,56(9):1459-1470
Satellite remote sensing offers new means of quantifying particulate organic carbon, POC, concentration over large oceanic areas. From SeaWiFS ocean color, we derived 10-year data of POC concentration in the surface waters of the global ocean. The 10-year time series of the global and basin scale average surface POC concentration do not display any significant long-term trends. The annual mean surface POC concentration and its seasonal amplitude are highest in the North Atlantic and lowest in the South Pacific, when compared to other ocean basins. POC anomalies in the North Atlantic, North Pacific, and global concentrations seem to be inversely correlated with El Niño index, but longer time series are needed to confirm this relationship. Quantitative estimates of POC reservoir in the oceanic surface layer depend on the choice of what should represent this layer. Global average POC biomass is 1.34 g m?2 if integrated over one optical depth, 3.62 g m?2 if integrated over mixed layer depth, and up to 6.41 g m?2 if integrated over 200-m layer depth (when assumed POC concentration below MLD is 20 mg m?3). The global estimate of total POC reservoir in the surface 200-m layer of the ocean is 228.61×1013 g. We expect that future estimates of POC reservoir may be even larger, when more precise calculations account for deep-water organic-matter maxima in oligotrophic regions, and POC biomass located just below the seasonal mixed layer in spring and summer in the temperate regions. 相似文献
10.
渤海颗粒有机碳与生物硅的分布及来源 总被引：2，自引：1，他引：1
海洋碳、硅循环及其相关联的生物地球化学过程是全球环境变化的热点问题,也是海洋科学关心的重要领域。利用2012年5月和11月份对渤海海域的调查结果,对该海域颗粒有机碳和生物硅的分布特征及来源进行了讨论。主要结论为:渤海有机碳以溶解有机碳为主,具有春季高和秋季低的特征;由陆地来源和海洋自生的有机碳组成,且以海洋来源的有机碳为主。渤海生物硅分布具有明显的梯度特征,河流输入同样对其含量的影响较为突出。渤海沉积物中生物硅含量较高,明显高于中国东部陆架海。渤海表层沉积物中生物硅主要是海源的,依次由浮游藻类、植硅体和海绵骨针所构成,其中浮游藻类占62.9%,陆源植硅体占31.1%。渤海沉积物发现了来自于草本植物的植硅体,这说明了陆地产生的植硅体对海洋生物硅的贡献。 相似文献
11.
春季东海北部近岸水体中的溶解无机碳和有机碳的分布特征及其影响因素 总被引：1，自引：0，他引：1
根据2010年4月在东海北部近岸的调查,分析了研究海域溶解无机碳（DIC）和溶解有机碳（DOC）的含量及其分布状况,并分别对DIC、DOC与温度、盐度、表观耗氧量等要素的关系进行了初步探讨。结果表明,春季研究海域表、底层DIC平均含量分别为24．54mg／L和25．03mg／L,平面分布趋势均为近岸高于远岸,象山口附近... 相似文献
12.
Reliable and consistent carbon fraction estimates are crucial in studying the role of coasts in the global carbon cycle. Remote sensing offers the potential to estimate carbon fractions with its advantages of large spatial coverage and real-time surveys. Colored dissolved organic matter (CDOM) absorption was generally used as a proxy to estimate dissolved organic carbon (DOC). However, the CDOM–DOC relationship varies by region and remains inconstant. Thus, the correlation between the reflectivity of visible band and DOC concentration was directly adopted in DOC estimation and performed well in former studies. Atomic groups of the various components of carbon fractions produce electronic transition by absorbing photons, and this process occurs both in the visible bands and in the near-infrared bands. Thus, the wide range of absorption band provides an approach to estimate carbon fractions using the correlation between the reflectivity of the whole visible/near-infrared bands of optical satellite sensors and carbon fractions. A new ratio band combination was developed and performed well in carbon fraction concentration retrievals, and the yielded estimation accuracies (R2?>?0.77, RPD >2.02) were sufficient to map the spatial distributions of carbon fractions with the moderate resolution imaging spectroradiometer image. 相似文献
13.
LIU Qiong PAN Delu BAI Yan WU Kai CHEN Chen-Tung Arthur SUN Jun ZHANG Lin 《海洋学报(英文版)》2013,32(2):1-11
The retrieval of dissolved organic carbon (DOC) distribution by remote sensing is mainly based on the empirical relationship of DOC concentration and colored dissolved organic matter (CDOM) concentration in many literatures. To investigate the nature of this relationship, the distributions and mixing behaviors of DOC and CDOM are reviewed in the world’s major estuaries and bays. It is found that, generally, the CDOM concentration is well correlated with the salinity in most estuaries, while DOC usually shows a nonconservative behavior which leads to a weak correlation between the DOC concentration and the CDOM concentration. To establish a good satellite reversion of the DOC concentration, the East China Sea(ECS) was taken as an example, and the mixing behavior of DOC and CDOM as well as the influence of biogeochemical processes were analyzed except for the physical mixing process with the data from late autumn (November, 2010) and winter (December, 2009) cruises. In the two ECS cruises, the CDOM concentration was found to be tightly correlated with the salinity, influenced little by the photochemical or biological processes. The data from the winter cruise show that DOC followed a conservative mixing along the salinity gradient, while in the late autumn cruise it was significantly affected by the biological activities, resulting in a poor correlation between the DOC and the CDOM. Accordingly, an improved DOC algorithm (CSDM) was proposed: when the biological influence was significant (Chl a greater than 0.8 μg/dm3 ), DOC was retrieved by the conservative and biological model, and if the conservative mixing was dominant (Chl a less than 0.8 μg/dm3 ), the direct DOC concentration and CDOM concentration relationship was used. Based on the proposed algorithm, a reasonable DOC distribution for the ECS from satellite was obtained in this study, and the proposed method can be applied to the other large river-dominant marginal sea. 相似文献
14.
南极普里兹湾及其邻近海域溶解有机碳的分布 总被引：5，自引：0，他引：5
中国南极科学考察第16航次期间(1999年11月～2000年4月),在南极普里兹湾及邻近海域的不同站位与水深采集海水样品用于溶解有机碳测定,通过高温催化氧化法完成样品的分析.结果表明,在调查期间,南极普里兹湾及其邻近海域各测站上层水体(0～100m)溶解有机碳浓度的变化范围为14.3～181.1μmol/dm3,平均为52.5μmol/dm3,该变化幅度比Ross海、太平洋等海域的相应值略大.溶解有机碳垂直分布的特征是0大于25大于50大于100m,即随深度的增加溶解有机碳浓度逐渐减小,与生物活动在垂直方向上的强弱变化相关.根据200m以深水柱溶解有机碳的垂直分布,可确定研究海域难降解溶解有机碳的浓度为40.4μmol/dm3,与其他研究所报道的数值(～42μmol/dm3)相近.上层水体(0～100m)过剩溶解有机碳的空间分布显示,64°S以北海域溶解有机碳过剩较多,而64°S以南海域则过剩溶解有机碳较少.溶解有机碳浓度与分布特征显示,普里兹湾及其邻近海域溶解有机碳浓度与南大洋其他海域相当,具有低溶解有机碳的一般特征.溶解有机碳浓度的空间分布呈现由西南向东北方向逐渐增加的趋势,这可能与南极陆架夏季上层水的北向扩展有关.生物活动及水体运动是研究海域溶解有机碳分布的主要影响因素. 相似文献
15.
海洋雾状层的成因及其对海洋碳循环过程的影响 总被引：2，自引：0，他引：2
海洋雾状层既是陆源物质进入海底的输送通道,又是海洋水体中沉降颗粒及底部再悬浮颗粒物的停留场所。雾状层物质来源主要有陆源、生源以及海底表层沉积物的再悬浮,不同海区、不同层位的雾状层的物质来源有所差异;雾状层的成因具有复杂性,既有物理作用,又有生物及化学作用,大量研究表明,海底洋流、内波(潮)等物理作用是雾状层形成的主要控制因素。雾状层中碳的存在形态主要有颗粒有机碳(POC)、溶解有机碳(DOC)、胶体有机碳(COC)以及无机碳,雾状层与其上下海水之间、雾状层与海底表层沉积物之间不同形态碳在生物-化学-物理动力系统作用下不断发生物质交换与迁移,对海洋碳循环生物地球化学过程起重要的控制作用,是整个海洋碳循环的一个不可忽视的环节。 相似文献
16.
《Deep Sea Research Part I: Oceanographic Research Papers》2000,47(1):137-158
The least known component of the “biological pump” is the active transport of carbon and nutrients by diel vertical migration of zooplankton. We measured CO2 respiration and dissolved organic carbon (DOC) excretion by individual species of common vertically migrating zooplankton at the US JGOFS Bermuda Atlantic Time-series Study (BATS) station. The inclusion of DOC excretion in this study builds on published research on active transport by respiration of inorganic carbon and allows a direct assessment of the role of zooplankton in the production of dissolved organic matter used in midwater microbial processes. On average, excretion of DOC makes up 24% (range=5–42%) of the total C metabolized (excreted+respired) and could represent a significant augmentation to the vertical flux that has already been documented for respiratory CO2 flux by migrant zooplankton. Migratory fluxes were compared to other transport processes at BATS. Estimates of combined active transport of CO2 and DOC by migrators at BATS averaged 7.8% and reached 38.6% of mean sinking POC flux at 150 m, and reached 71.4% of mean sinking POC flux at 300 m. DOC export by migrator excretion averaged 1.9% and reached 13.3% of annual DOC export by physical mixing at this site. During most of the year when deep mixing does not occur, diel migration by zooplankton could provide a supply of DOC to the deeper layers that is available for use by the microbial community. A carbon budget comparing migrant zooplankton transport to the balance of fluxes in the 300–600 m depth strata at BATS shows on average that the total migrant flux supplies 37% of the organic carbon remineralized in this layer, and that migrant DOC flux is more than 3 times the DOC flux gradient by diapycnal mixing. New estimates of active transport of both organic and inorganic carbon by migrants may help resolve observed imbalances in the C budget at BATS, but the magnitude is highly dependent on the biomass of the migrating community. 相似文献
17.
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
18.
Dissolved organic carbon (DOC) is a carbon reservoir that is as large as the atmospheric CO2 pool, and its contribution to the global carbon cycle is gaining attention. As DOC is a dissolved tracer, its distribution can serve to trace the mixing of water masses and the pathways of ocean circulation. Published proxy and model reconstructions have revealed that, during the last glacial maximum (LGM), the pattern of deep ocean circulation differed from that of the modern ocean, whereby additional carbon is assumed to have been sequestered in stratified LGM deep water. The aim of this study is to explore the distribution of DOC and its production/removal rate during the LGM using the Grid ENabled Integrated Earth system model (GENIE). Modeled results reveal that increased salinity of bottom waters in the Southern Ocean is associated with stronger stratification and oxygen depletion. The stratified LGM deep ocean traps more nutrients, resulting in a decrease in the DOC reservoir size that, in turn, causes a negative feedback for carbon sequestration. This finding requires an increase in DOC lifetime to compensate for the negative feedback. The upper limit of DOC lifetime is assumed to be 20,000 years. Modeled results derive an increase (decrease) in DOC reservoir by 100 Pg C leading to an atmospheric CO2 decrease (increase) of 9.1 ppm and a dissolved inorganic carbon δ13C increase (decrease) of 0.06‰. The DOC removal rate is estimated to be 39.5 Tg C year–1 in the deep sea during the LGM. The contribution of DOC to the LGM carbon cycle elucidates potential carbon sink-increasing strategies. 相似文献
19.
Masahide Wakita Makio C. Honda Kazuhiko Matsumoto Tetsuichi Fujiki Hajime Kawakami Sayaka Yasunaka Yoshikazu Sasai Chiho Sukigara Mario Uchimiya Minoru Kitamura Toru Kobari Yoshihisa Mino Akira Nagano Shuichi Watanabe Toshiro Saino 《Journal of Oceanography》2016,72(5):665-685
The annual flux of biologically produced organic carbon from surface waters is equivalent to annual net community production (NCP) at a steady state and equals the export of particulate and dissolved organic carbon (POC and DOC, respectively) to the ocean interior. NCP was estimated from carbon budgets of salinity-normalized dissolved inorganic carbon (nDIC) inventories at two time-series stations in the western subarctic (K2) and subtropical (S1) North Pacific Ocean. By using quasi-monthly biogeochemical observations from 2004 to 2013, monthly mean nDIC inventories were integrated from the surface to the annual maximum mixed layer depth and corrected for changes due to net air–sea CO2 exchange, net CaCO3 production, vertical diffusion from the upper thermocline, and horizontal advection. The annual organic carbon flux at K2 (1.49 ± 0.42 mol m?2 year?1) was lower than S1 (2.81 ± 0.53 mol m?2 year?1) (p < 0.001 based on t test). These fluxes consist of three components: vertically exported POC fluxes (K2: 1.43 mol m?2 year?1; S1: 2.49 mol m?2 year?1), vertical diffusive DOC fluxes (K2: 0.03 mol m?2 year?1; S1: 0.25 mol m?2 year?1), and suspended POC fluxes (K2: 0.03 mol m?2 year?1; S1: 0.07 mol m?2 year?1). The estimated POC export flux at K2 was comparable to the sum of the POC flux observed with drifting sediment traps and active carbon flux exported by migrating zooplankton. The export fluxes at both stations were higher than those reported at other time-series sites (ALOHA, the Bermuda Atlantic Time-series Study, and Ocean Station Papa). 相似文献
20.
目前,溶解有机碳(DOC)遥感反演研究主要集中在河口及陆源影响较大的边缘海区,大多数是利用DOC与有色溶解有机物(CDOM)或DOC与盐度的经验关系获取。为了较好的理解DOC的遥感反演机理,收集了全球主要大河(流量排名前25中16条)及边缘海DOC与CDOM浓度与保守性分布状况,发现大多数河口CDOM呈现保守性分布,DOC呈现非保守性分布。基于DOC与CDOM保守性行为的主要影响因素分析以及研究海区的生物地球化学特征,论述了DOC遥感反演算法的研究进展,提出了DOC遥感反演需要考虑DOC受不同主要控制因素(如保守混合与生物作用等)的影响,并对这些控制因素进行量化。 相似文献