Hydrography of chromophoric dissolved organic matter in the North Atlantic

The distribution and optical absorption characteristics of chromophoric dissolved organic matter (CDOM) were systematically investigated along three meridional transects in the North Atlantic Ocean and Caribbean Sea conducted as part of the 2003 US CLIVAR/CO₂ Repeat Hydrography survey. Hydrographic transects covered in aggregate a latitudinal range of 5° to 62° north along longitudes 20°W (line A16N, Leg 1), 52°W (A20), and 66°W (A22). Absorption spectra of filtered seawater samples were collected and analyzed for depths ranging from the surface to ∼6000 m, sampling all the ocean water masses in the western basin of the subtropical North Atlantic and several stations on the North and South American continental slopes. The lowest surface abundances of CDOM (< 0.1 m⁻¹ absorption coefficient at 325 nm) were found in the central subtropical gyres while the highest surface abundances (∼0.7 m⁻¹) were found along the continental shelves and within the subpolar gyre, confirming recent satellite-based assessments of surface CDOM distribution. Within the ocean interior, CDOM abundances were relatively high (0.1–0.2 m⁻¹ absorption coefficient at 325 nm) except in the subtropical mode water, where a local minimum exists due to the subduction of low CDOM surface waters during mode water formation. In the subthermocline water masses of the western basin, changes in CDOM abundance are not correlated with increasing ventilation age as assessed using chlorofluorocarbon (CFC) concentrations and the atmospheric CFC history. But dissolved organic carbon (DOC) mass-specific absorption coefficients of CDOM increase with increasing ventilation age in the deep sea, indicating that CDOM is a refractory component of the DOC pool. The overall CDOM distribution in the North Atlantic reflects the rapid advection and mixing processes of the basin and demonstrates that remineralization in the ocean interior is not a significant sink for CDOM. This supports the potential of CDOM as a tracer of ocean circulation processes for subducted water masses.     

Vertical and horizontal distribution of fluorescent dissolved organic matter in the Southern Ocean

The vertical and horizontal distribution of fluorescent dissolved organic matter (FDOM), determined by fluorescence intensity at 320 nm excitation and 420 nm emission, were clarified in nine stations on two transects at the Southern Ocean, including a subtropical, subantarctic, polar frontal and Antarctic zone. All vertical profiles of fluorescence intensity showed that levels were lowest in the surface waters, increased with increasing the depth in mid-depth waters ( 2000 m), and then stayed within a relatively narrow range from there to the bottom. Such vertical profiles of FDOM were similar to those of nutrients, but were adverse to dissolved oxygen. In water columns below the temperature-minimum subsurface water (dichothermal waters) in the Antarctic zone and below the winter mixed layer in the other zones, we determined the relationships of fluorescence intensity to concentrations of nutrients and apparent oxygen utilization (AOU) over the entire area of the present study, and found significant linear correlations between the levels of fluorescence intensity and nutrient concentrations (r =  0.70 and 0.71 for phosphate and nitrate + nitrite, respectively) and AOU (r = 0.91). From the strong correlation coefficient between fluorescence intensity and AOU, we concluded that FDOM in the Southern Ocean is formed in situ via the biological oxidation of organic matter. The regeneration of the nutrients/consumption of the oxygen/formation of FDOM was active in mid-depth waters. However, the correlations between fluorescence intensities and nutrients and AOU were different in the mid-depth water masses, Subantarctic Mode Water (SAMW), and Antarctic Intermediate Water (AAIW), indicating that the sources of organic matter responsible for FDOM formation were different. A considerable amount of FDOM in the SAMW is thought to be produced by the remineralization of DOM in addition to sinking particulate organic matter, while DOM is less responsible for FDOM formation in the AAIW.     

水体中有色可溶性有机物的研究进展

有色可溶性有机物(CDOM)是水体中一类重要的光吸收物质,在短波的吸收大大降低了紫外辐射在水体的衰减,因而其光学行为和生物地球化学循环将对水体生态系统产生重要影响。CDOM在水体生态系统、水色遥感和全球碳循环研究中具有广阔的应用前景。文章综述了国内外CDOM研究现状与动态,其中包括CDOM的光吸收特性、荧光特性、光化学降解以及CDOM和DOC浓度的水色遥感,最后提出在内陆水体湖泊中开展CDOM研究的设想。     

Release of dissolved organic matter during oxic and anoxic decomposition of salt marsh cordgrass

Chromophoric dissolved organic matter (CDOM), as the light absorbing fraction of bulk dissolved organic matter (DOM), plays a number of important roles in the global and local biogeochemical cycling of dissolved organic carbon (DOC) and in controlling the optical properties of estuarine and coastal waters. Intertidal areas such as salt marshes can contribute significant amounts of the CDOM that is exported to the ocean, but the processes controlling this CDOM source are not well understood. In this study, we investigate the production of DOM and CDOM from the decomposition of two salt marsh cordgrasses, Spartina patens, a C₄ grass, and Typha latifolia, a C₃ grass, in well-controlled laboratory experiments. During the seven-week incubation period of the salt marsh grasses in oxic and anoxic seawater, changes in dissolved organic carbon (DOC) concentrations, dissolved nitrogen (DN) concentrations, stable carbon isotopic composition of DOC (DOC-δ¹³C), and CDOM fluorescence demonstrate a significant contribution of DOC and CDOM to estuarine waters from salt marsh plants, such as Spartina and Typha species. In the natural environment, however, the release processes of CDOM from different cordgrass species could be controlled largely by the in situ oxic and anoxic conditions present during degradation which affects both the production and decomposition of DOC and CDOM, as well as the optical properties of CDOM in estuarine and coastal waters.     

Roles of Biogeochemical Processes in the Oceanic Carbon Cycle Described with a Simple Coupled Physical-Biogeochemical Model

To evaluate the contribution of biogeochemical processes to the oceanic carbon cycle and to calculate the ratio of calcium carbonate to organic carbon downward export, we have incorporated biological and alkalinity pumps in the yoked high-latitude exchange/interior diffusion-advection (YOLDA) model. The biogeochemical processes are represented by four parameters. The values of the parameters are tuned so that the model can reproduce the observed phosphate and alkalinity distributions in each oceanic region. The sensitivity of the model to the biogeochemical parameters shows that biological production rates in the euphotic zone and decomposition depths of particulate matters significantly influence horizontal and vertical distributions of biogeochemical substances. The modeled vertical fluxes of particulate organic phosphorus and calcium carbonate are converted to vertical carbon fluxes by the biological pump and the alkalinity pump, respectively. The downward carbon flux from the surface layer to the deep layer in the entire region is estimated to be 3.36 PgC/yr, which consists of 2.93 PgC/yr from the biological pump and 0.43 PgC/yr from the alkalinity pump, which is consistent with previous studies. The modeled rain ratio is higher with depth and higher in the Pacific and Indian Oceans than in the Atlantic Ocean. The global rain ratio at the surface layer is calculated to be 0.14 to 0.15. This value lies between the lower and higher ends of the previous estimates, which range widely from 0.05 to 0.25. This study indicates that the rain ratio is unlikely to be higher than 0.15, at least in the surface waters.     

The fluorescence of dissolved organic matter in seawater

A total of 28 vertical profiles of seawater fluorescence was measured in the Sargasso Sea, the Straits of Florida, the Southern California Borderlands, and the central Pacific Ocean. In all cases, surface seawater fluorescence was low as a result of photochemical bleaching which occurs on the timescale of hours. Fluorescence of deep water was 2–2.5 times higher than that of surface waters, and was constant, implying a long residence time for fluorescent organic matter, possibly of the order of thousands of years. Fluorescence correlates well with nutrients (NO₃⁻, PO₄³⁻) in mid-depth waters (100–1000 m) in the Sargasso Sea and the central North Pacific, consistent with results in the central Pacific and the coastal seas of Japan. This suggests that regeneration or formation of fluorescent materials accompanies the oxidation and remineralization of settling organic particles.The various sources and sinks of fluorescent organic matter in the global oceans are assessed. The major sources are particles and in situ formation; rivers, rain, diffusion from sediments, and release from organisms are minor sources. The major sink is photochemical bleaching.     

Oxygen Utilization and Organic Carbon Remineralization in the Upper Water Column of the Pacific Ocean

As a part of the JGOFS synthesis and modeling project, researchers have been working to synthesize the WOCE/JGOFS/DOE/NOAA global CO₂ survey data to better understand carbon cycling processes in the oceans. Working with international investigators we have compiled a Pacific Ocean data set with over 35,000 unique samples analyzed for at least two carbon species, oxygen, nutrients, chlorofluorocarbon (CFC) tracers, and hydrographic parameters. We use these data here to estimate in-situ oxygen utilization rates (OUR) and organic carbon remineralization rates within the upper water column of the Pacific Ocean. OURs are derived from the observed apparent oxygen utilization (AOU) and the water age estimates based on CFCs in the upper water and natural radiocarbon in deep waters. The rates are generally highest just below the euphotic zone and decrease with depth to values that are much lower and nearly constant in water deeper than 1200 m. OURs ranged from about 0.02–10 μmol kg⁻¹yr⁻¹ in the upper water masses from about 100–1000 m, and averaged = 0.10 μmol kg⁻¹yr⁻¹ in deep waters below 1200 m. The OUR data can be used to directly estimate organic carbon remineralization rates using the C:O Redfield ratio given in Anderson and Sarmiento (1994). When these rates are integrated we obtain an estimate of 5.3 ± 1 Pg C yr⁻¹ for the remineralization of organic carbon in the upper water column of the Pacific Ocean. This revised version was published online in July 2006 with corrections to the Cover Date.     

CMIP5地球系统模式溶解氧模拟结果分析

本文基于常用的统计方法,通过与WOA09观测的海洋溶解氧浓度数据进行比较,定量地评估了9个CMIP5地球系统模式在历史排放试验中海洋溶解氧气候态特征的模拟能力。在海表,由于地球系统模式均能很好地模拟海表温度（SST）,模式模拟的海表溶解氧浓度分布与观测一致,模拟结果无论是全球平均浓度偏差还是均方根误差均接近0,空间相关系数与标准偏差接近1。在海洋中层以及深层这些重要水团所在的区域,各模式的模拟能力则差异较大,尤其在溶解氧低值区（OMZs）所在的500m到1000m,各模式均出现全球平均偏差、均方根误差的极大值以及空间相关系数的极小值。在海洋内部,模式偏差的原因比较复杂。经向翻转环流和颗粒有机碳通量均对模式的偏差有贡献。分析结果表明物理场偏差对溶解氧偏差的贡献较大。一些重要水团,比如北大西洋深水,南极底层水以及北太平洋中层水在极大程度上影响了溶解氧在这些海区的分布。需要指出的是,虽然在海洋内部各模式模拟的溶解氧浓度偏差较大,但是多模式平均结果却能表现出与观测较好的一致性。     

Formation and transport of intermediate water masses in a model of the Pacific Ocean

A basin-wide ocean general circulation model of the Pacific Ocean was used to investigate how the interior restoration in the Okhotsk Sea and the isopycnal diffusion affect the circulation and intermediate water masses. Four numerical experiments were conducted, including a run with the same isopycnal and thickness diffusivity of 1.0×103 m2/s, a run employing the interior restoration of temperature and salinity in the Okhotsk Sea with a time scale of 3 months, a run that is the same as the first run except for the enhanced isopycnal mixing, and a final run with the combination of the restoration in the Okhotsk Sea and large isopycnal diffusivity. Simulated results show that the intermediate water masses reproduced in the first run are relatively weak. An increase in isopycnal diffusivity can improve the simulation of both Antarctic and North Pacific intermediate waters, mainly increasing the transport in the interior ocean, but inhibiting the outflow from the Okhotsk Sea. The interior restoration generates the reverse current from the observation in the Okhotsk Sea, whereas the simulation of the temperature and salinity is improved in the high latitude region of the Northern Hemisphere because of the reasonable source of the North Pacific Intermediate Water. A comparison of vertical profiles of temperature and salinity along 50°N between the simulation and observations demonstrates that the vertical mixing in the source region of intermediate water masses is very important.     

Export Production in the Equatorial and North Pacific Derived from Dissolved Oxygen, Nutrient and Carbon Data

A global ocean inverse model that includes the 3D ocean circulation as well as the production, sinking and remineralization of biogenic particulate matter is used to estimate the carbon export flux in the Pacific, north of 10°S. The model exploits the existing large datasets for hydrographic parameters, dissolved oxygen, nutrients and carbon, and determines optimal export production rates by fitting the model to the observed water column distributions by means of the “adjoint method”. In the model, the observations can be explained satisfactorily with an integrated carbon export production of about 3 Gt C yr⁻¹ (equivalent to 3⋅10¹⁵ gC yr⁻¹) for the considered zone of the Pacific Ocean. This amounts to about a third of the global ocean carbon export of 9.6 Gt C yr⁻¹ in the model. The highest export fluxes occur in the coastal upwelling region off northwestern America and in the tropical eastern Pacific. Due to the large surface area, the open-ocean, oligotrophic region in the central North Pacific also contributes significantly to the total North Pacific export flux (0.45 Gt C yr⁻¹), despite the rather small average flux densities in this region (13 gC m⁻²yr⁻¹). Model e-ratios (calculated here as ratios of model export production to primary production, as inferred from satellite observations) range from as high a value as 0.4 in the tropical Pacific to 0.17 in the oligotrophic central north Pacific. Model e-ratios in the northeastern Pacific upwelling regions amount to about 0.3 and are lower than previous estimates. This revised version was published online in July 2006 with corrections to the Cover Date.     

Fluorescence characteristics of dissolved organic matter in the deep waters of the Okhotsk Sea and the northwestern North Pacific Ocean

Fluorescent dissolved organic matter (DOM), a fraction of chromophoric DOM, is known to be produced in the deep ocean and is considered to be bio-refractory. However, the factors controlling fluorescence properties of DOM in the deep ocean are still not well understood. In this study, we determined the fluorescence properties of DOM in the deep waters of the Okhotsk Sea and the northwestern North Pacific Ocean using excitation-emission matrix (EEM) fluorescence and parallel factor analysis (PARAFAC). One protein-like, two humic-like components, and one uncertain component, which might be derived from a fluorometer artifact, were identified by EEM-PARAFAC. Fluorescence intensity levels of the protein-like component were highest in the surface waters, decreased with depth, but did not change systematically in the bathypelagic layer (1000 m - bottom). Fluorescence characteristics of the two humic-like components were similar to those traditionally defined as marine and terrestrial humic-like fluorophores. The fluorescence intensity levels of the two humic-like components were lowest in the surface waters, increased with depth in the mesopelagic layer (200 - 1000 m), and then slightly decreased with depth in the bathypelagic layer. The ratio of the two humic-like components remained in a relatively narrow range in the bathypelagic layer compared to that in the surface layer, suggesting a similar composition of humic-like fluorophores in the bathypelagic layer. In addition, the fluorescence intensities of the two humic-like components were linearly correlated to apparent oxygen utilization (AOU) in the bathypelagic layer, suggesting that both humic-like components are produced in situ as organic matter is oxidized biologically. These findings imply that optical characteristics of humic-like fluorophores once formed might not be altered further biologically or geochemically in the deep ocean. On the other hand, relationships of fluorescence intensities with AOU and Fe(III) solubility were different between the two humic-like components in the mesopelagic layer, suggesting different environmental dynamics and biogeochemical roles for the two humic-like components.     

Understanding the export of biogenic particles in oceanic waters: Is there consensus?

We examine progress towards a global view of oceanic export of particulate organic carbon (POC) and other nutrient elements (P, N, Si) from the surface (upper 100 m), through the subsurface, to the deep sea (>1000 m), focusing on syntheses published since 1999 and on the Joint Global Ocean Flux Study. Food-web structure is important, and surface and subsurface processes contribute similarly to determine the fraction of net primary production (NPP) reaching the deep sea. NPP by large cells generally favours high surface export of POC. Preferential remineralization of P and N (versus C) with depth is common, as is regional variation in subsurface POC flux attenuation.The role of mineral fluxes is complex. Annual mean fluxes of POC and minerals are correlated in global deep sediment trap records, but causality and the relative importance of different minerals depends on the assumptions made. Time-series observations at single sites can oppose the geographic trends, and their large seasonal variability in the contribution of POC to total flux is at odds with mechanistic models for POC transport by minerals. Despite generally positive correlations between biogenic carbonate and POC fluxes, the overall role of carbonate export is to decrease the transfer of carbon dioxide from the atmosphere to the ocean. Both autotrophs and heterotrophs produce minerals, and progress in separating these contributions is required for the deconvolution of mineral ballast and food-web effects.Many recent models suggest global surface POC export of ∼10 GTC/yr, despite widely varying biological complexity. This limits the usefulness of their prediction of ecosystem and carbon cycle responses to global change. Progress requires better observations for model validation, and more efforts to relate the models to the observed complexity, rather than to overly simplified global syntheses. We advocate more time-series stations targeting under-studied biogeochemical regions, development of automated in situ tools for study of the subsurface ocean, and increased emphasis on combining ecological and biogeochemical methods.     

Dynamics and elemental stoichiometry of carbon,nitrogen, and phosphorus in particulate and dissolved organic pools during a phytoplankton bloom induced by in situ iron enrichment in the western subarctic Pacific (SEEDS-II)

The dynamics of organic carbon (C), nitrogen (N), and phosphorus (P) were examined during an in situ mesoscale iron-enrichment experiment in the western North Pacific in the summer of 2004. We separately determined the production of particulate organic matter (POM) and dissolved organic matter (DOM) and their subsequent removal during the bloom decline. As the iron-induced phytoplankton bloom progressed (days 0–14), POM increased in the surface mixed layer, while DOM did not increase significantly. The molar ratios for C:N, C:P, and N:P of the newly produced POM were estimated to be 4.9, 190, and 37 in the surface mixed layer, whereas the dissolved inorganic nitrogen to soluble reactive phosphorus drawdown ratio was 17. Preferential remineralization of P over C and N from the POM was postulated during the developing phytoplankton bloom. During the bloom decline (days 16–25), surface POM decreased with a similar C:N of 5.2. The N:P ratio of surface DOM increased during the bloom decline. Below the surface mixed layer, DOC and DON increased moderately after the peak of the bloom. The time-series variation of DOC and DON was not identical. The C, N, and P dynamics through the accumulation and removal of POM and DOM were complex. Grazing by mesozooplankton during the experiment may have played a significant role in the uncoupling of the dynamics of C, N, and P.     

大河影响下的陆架边缘海沉积有机碳的再矿化作用

大河影响下的陆架边缘海(RiOMars)是陆源有机碳的主要沉积汇,是陆海相互作用最重要的区域,在全球碳的生物地球化学循环中发挥着重要作用。受到RiOMars系统内频繁的物理和生物等改造作用的影响,该区沉积的有机碳并没有得到很好地保存而被永久埋藏,而是发生了显著的再矿化分解。本文首先对目前常用的基于O2消耗速率和CO2产生速率的两类测定RiOMars系统沉积有机碳再矿化速率的方法进行了介绍,分析了各自的优缺点和适用性,进而从碳的形态转化、表层沉积物混合均匀、形成次氧化的氧化还原条件、有机碳保存效率低、发生反风化作用和微生物发挥着重要作用等几个方面对RiOMars系统沉积物发生再矿化作用时的主要过程和特征进行了剖析,以期深入认识边缘海的再矿化作用及其对边缘海碳汇的影响。     

Vertical distribution of dissolved organic carbon (DOC) in the Western Mediterranean Sea in relation to the hydrological characteristics

Vertical profiles of dissolved organic carbon (DOC) from eight hydrological stations in the Tyrrhenian Sea, Sardinia Channel and Algerian Sea, are reported. DOC exhibits concentrations ranging from 58 to 88 μM in surface water, 43–57 μM in the intermediate layer and 49–63 μM in deep waters. The assessment of the hydrological characteristics allows different water masses in the study area to be identified; moreover, different hydrological processes are observed in the Tyrrhenian and Algerian basins. DOC exhibits different values in the different water masses. The lowest DOC concentrations (43–46 μM) were found in the Tyrrhenian Levantine Intermediate Water (LIW). Correlations between DOC and apparent oxygen utilization (AOU), investigated within each water mass, exhibit different behaviors in the intermediate and deep waters, suggesting the occurrence of different processes of oxygen consumption in the different water masses.     

西太平洋冬季上层水体有色溶解有机物的分布和转化特征

为深入解析西太平洋溶解有机碳的生物地球化学过程，本研究于2015年12月至2016年1月，开展了西太平洋上层水体有色溶解有机物（CDOM）吸收光谱和荧光光谱特征研究。研究结果表明，西太平洋上层水体CDOM吸收系数a（320）变化范围为0.01~1.07 m-1，平均值为0.18 m-1；其较高值位于100~200 m水层，表层的海水相对含量较低，主要以有机物的光化学分解为主。采用PARAFAC分析CDOM三维荧光光谱特征，得到1种类腐殖质组分C2（252（310 nm）/405 nm）及2种类蛋白组分C1（224（276 nm）/335 nm）和C3（224（260 nm）/300 nm），其中类腐殖质荧光组分占总荧光强度的11%~22%，蛋白质荧光组分占总荧光强度的78%~89%，蛋白质荧光中类色氨酸和类络氨酸组分对荧光强度的贡献相当。洋流在大尺度上控制西太平洋CDOM的分布特征，两流交界处和环流形成区域的CDOM相对含量较高，荧光信号较强。西太上层水体CDOM相对含量和荧光信息，与温度、盐度、DO和营养盐等理化因素之间的相关分析结果表明，CDOM主要成分类蛋白质的产生主要受上层水体初级生产过程控制。     

Tracing dissolved organic matter cycling in the eastern boundary of the temperate North Atlantic using absorption and fluorescence spectroscopy

Apparent oxygen utilization (AOU), dissolved organic carbon (DOC), coloured dissolved organic matter (CDOM) absorption spectra, and CDOM fluorescence characteristic of aromatic amino acids (excitation/emission 280 nm/320 nm; F(280/320)) and marine-humic like substances (320 nm/410 nm; F(320/410)) were measured in full depth during a cruise in the temperate Eastern North Atlantic (ENA). An optimum multi-parameter (OMP) inverse method was run to calculate water mass proportion-weighted average (archetypal) concentrations of these chemical parameters for all water masses and samples. Archetypal concentrations retain the variability due to water mass mixing and basin scale mineralization from the water mass formation sites to the study area. Conversely, the difference between measured and archetypal concentrations, retain the variability due to dissimilarities in mineralization processes within the study area. Our analysis indicates that DOC supported 26±3% of the AOU in the dark temperate ENA and that basin scale processes occurring at and from the formation area of the water masses explained 63% of the total DOC variability. Our data also suggests that DOC remineralized at the basin scale was of lower molecular weight, and with a lower proportion of fluorescent aromatic amino acids than found within the study area. The relationship between the absorption coefficient at 254 nm (a_CDOM(254)) and AOU indicates that a_CDOM(254) was consumed during organic matter remineralization in the dark ocean, with 55% of the variability being explained by basin scale processes. The relationships of F(320/410) with AOU and DOC confirmed that marine humic-like substances are produced by microbial degradation processes, at a rate of 6.1±0.9×10⁻³ mg equivalents of QS mol AOU⁻¹. Our results also indicate that basin-scale remineralization processes account for 85% of the total variability of F(320/410), emphasizing that large scale processes control the formation of humic-like substance in the dark ENA.     

Temporal Trends in Apparent Oxygen Utilization in the Upper Pycnocline of the North Pacific: 1980–2000

We present a compilation of apparent oxygen utilization (AOU) changes observed in the upper pycnocline of the North Pacific Ocean over the last several decades. The goal here is to place previously-published data in a common format, and assess the causes of the observed changes. The general trend along repeat cross sections of the eastern and western subtropical ocean and the subarctic ocean is an increase in AOU from the mid 1980s to the mid 1990s. AOU has also been increasing in a time-series study in the northwest subarctic Ocean off of Japan since the late 1960s. Observed AOU changes south of 35°N in the subtropical ocean are 10–20 μmol kg⁻¹, with much greater changes, reaching 60–80 μmol kg⁻¹ in isolated areas, in the subtropical/subarctic boundary and the subarctic ocean. Analysis of changes in both AOU and salinity on isopycnals suggests that there are significant salinity-normalized increases that must be due to alteration in the rate of ventilation or organic matter degradation. A common feature in the data is that the maximum increase in AOU is centered near the density horizon σ_θ= 26.6. Time series results from the Oyashio Current region near the winter outcrop area of this density horizon indicate that surface waters there have become fresher with time, which may mean this density surface has ceased to outcrop in the latter decades of the 20th century. Whether this is due to natural decadal-scale changes or anthropogenic influences can be decided by determining future trends in AOU on these density surfaces. This revised version was published online in July 2006 with corrections to the Cover Date.     

The Western North Pacific Playing a Key Role in Global Biogeochemical Fluxes

The oceanic biogeochemical fluxes in the North Pacific, especially its northwestern part, are discussed to prove their importance on a global scale. First, the air-sea exchange processes of chemical substances are considered quantitatively. The topics discussed are sea salt particles transported to land, sporadic transport of soil dust to the ocean and its role in the marine ecosystem, the larger gas transfer velocity of CO₂ indicating the effect of bubbles, and DMS and greenhouse gases other than CO₂. Next, chemical tracers are utilized to reveal the water circulation systems in the region, which are the Pacific Deep Water including its vertical eddy diffusivity, the North Pacific Intermediate Water and the Japan Sea Deep Water. Thirdly, the particulate transport process of chemical substances through the water column is clarified by analyzing the distribution of insoluble radionuclides and the results obtained from sediment trap experiments. Fourthly, the northern North Pacific is characterized by stating the site decomposing organic matter and Si playing a key role in the marine ecosystem. Both are induced by the upwelled Pacific Deep Water. Fifthly, the oceanic CO₂ system related to global warming is presented by clarifying the distribution of anthropogenic CO₂ in the western North Pacific, and roles of the upwelled Pacific Deep Water and the continental shelf zone in the absorption of atmospheric CO₂. Finally, Mn and other chemical substances in sediments are discussed as recorders of the early diagenesis and indicators of low biological productivity during glacial ages in the northwestern North Pacific. It is concluded that the western North Pacific is characterized mainly by the Pacific Deep Water bringing nutrients to the northern North Pacific, located at the exit of the global deep water circulation and, therefore, the region plays a key role in the global biogeochemical fluxes. This revised version was published online in August 2006 with corrections to the Cover Date.     

The importance of subsurface nepheloid layers in transport and delivery of sediments to the eastern Cariaco Basin,Venezuela

Optical transmissometer measurements were coupled with particulate organic matter (POM) observations to understand suspended sediment composition and distribution in the eastern Cariaco Basin during the rainy seasons of September 2003 and 2006. Our results suggest that nepheloid layers originating at the mouth of small mountainous rivers discharging into the eastern Basin are a major delivery mechanism of terrigenous sediments to the Basin interior. Intermediate nepheloid layers (INL) were observed near the shelf break (～100 m) and appear to effectively transport terrigenous material laterally from the shelf to deep waters, thereby providing a plausible supply mechanism of the terrestrial material observed in sediment traps. These findings highlight the importance of small, local rivers in the Cariaco Basin as sources of terrestrial material. In contrast, these nepheloid layers contained only limited POM. When this information is combined with published sediment trap POM data, it suggests that nepheloid layers may not be a primary mechanism for delivering terrigenous POM to the deeper waters of the basin during the rainy season. Rather, BNL may redistribute marine-derived POM from shallow waters to the Basin's interior by providing ballast materials, particularly during episodic events driven by wind and precipitation. Though we have determined that nepheloid layers play an important role in the seaward transport of particulate material in the Cariaco Basin, their composition and temporal variability have not been fully characterized. This is critical to understand lateral particle transport, since nepheloid layers constitute a significant source of sediment to the deep Cariaco Basin.