南大洋普里兹湾基于234Th/238U不平衡法的POC输出通量研究

中国第22次南极科学考察(2005年11月至2006年3月)期间,测定了南极普里兹湾海域5个站位的从表层至150 m水深的不同层位水样中溶解态和颗粒态234Th,238U的放射性比活度以及颗粒有机碳.利用234Th/238U在上层水体中的不平衡,计算了南极普里兹湾上层水体中234Th的平均停留时间和输出通量.结果显示,随着纬度的增加,上层水体中颗粒态和溶解态234Th的平均停留时间总体趋向减小,并在中纬度站位出现了最低值,分别为1~8和29~48 d,而颗粒态和溶解态234Th的输出通量则在中纬度站位出现了最大值,分别为21~38和26~39 dpm/(m3·d).运用箱型清除模式,利用两种不同的方法估算了各水柱中从真光层底部输出的POC通量,平均值分别达到104.7 mmol/(m2·d)(E法)和120.6 mmol/(m2·d)(B法),表明南极普里兹湾夏季存在很高的新生产力,它将会对该海域碳的生物泵过程产生重要作用.     

POC fluxes from euphotic zone estimated from 234Th deficiency in winter in the northwestern North Pacific Ocean

1IntroductionThefluxesofcarbon,nutrients,andassoci-atedelementsinvolvedinthebiogeochemicalcyclesoutoftheeuphoticzoneareimportantinthestudyofglobalCO2 change.Someworkershaveproposedthatatthesteadystatethefluxofparticulateorganiccarbonoutoftheeuphoticzoneequalsthenewproduction(EppleyandPe-terson,1979;Eppley,1989).Generallytwometh-odscanbeemployedtoobtainthefluxdata.Oneistousesedimenttrapsintheupperocean(<200m)orfloatingsedimenttraps.Thoughthesedimenttraptechnologyhasshowntobeuse-fulfortimeser…     

234 Th示踪法测定北太平洋西北海域冬季真光层中颗粒态有机碳输出通量

讨论了1997年冬季在北太平洋西北海域7个站位的表层至200m水深水柱中溶解及颗粒态234Th,颗粒态有机碳(POC)、氮(PON)及叶绿素a浓度的垂直分布剖面.溶解态、颗粒态及总的234Th的放射性在真光层中显著低于母体238U的放射性,总的234Th放射性在水深大于100m时趋于平衡.利用234Th-238U在海洋表层海水中的放射性不平衡推导出了北太平洋西北海域冬季真光层海水中234Th的平均停留时间和输出通量以及颗粒态有机碳和有机氮的输出通量.在亚北极环流区溶解态234Th的停留时间为40~50d,而在黑潮-亲潮共同影响区为20d左右.颗粒态有机碳和有机氮从真光层的输出通量范围分别为3.8~8.2和0.50~0.98mmol/(m2·d),西部海区高于东部海区,南部海区高于北部海区.在黑潮-亲潮共同影响区较高的颗粒态有机碳输出通量表明光照量及陆源营养盐物质的提供是两个决定生产力的主要因素.叶绿素a的水深分布和POC/PON的值同Redfield的比值的一致性表明这个海区的冬季颗粒物主要由浮游植物构成.北太平洋西北海域在冬季的颗粒有机碳输出通量可高于世界大洋一些海区春、夏季的颗粒有机碳输出通量.     

Air-sea carbon fluxes and their controlling factors in the Prydz Bay in the Antarctic

The Prydz Bay in the Antarctic is an important area in the Southern Ocean due to its unique geographic feature. It plays an important role in the carbon cycle in the Southern Ocean. To investigate the distributions of carbon dioxide in the atmosphere and surface seawater and its air-sea exchange rates in this region, the Chinese National Antarctic Research Expedition （CHINARE） had set up several sections in the Prydz Bay. Here we present the results from the CHINARE-XVI cruises were presented onboard R/V Xue/ong from November 1999 to April 2000 and the main driving forces were discussed controlling the distributions of partial pressure of carbon dioxide. According to the partial pressure of carbon dioxide distributions, the Prydz Bay can be divided into the inside and outside regions. The partial pressure of carbon dioxide was low in the inside region but higher in the outside region during the measurement period. This distribution had a good negative correlation with the concentrations of ehlorophyll-a in general, suggesting that the partial pressure of carbon dioxide was substantially affected by biological production. The results also indicate that the biological produetion is most likely the main driving force in the marginal ice zone in the Southern Ocean in summer. However, in the Antarctic divergence sector of the Prydz Bay （about 64°S）, the hydrological processes become the controlling factor as the sea surface partial pressure of carbon dioxide is much higher than the atmospheric one due to the upwelling of the high DIC CDW, and this made the outside of Prydz Bay a source of carbon dioxide. On the basis of the calculations, the CO2 flux in January （austral summer） was -3.23 mmol/（m^2 · d） in the inner part of Prydz Bay, i.e. , a sink of atmospheric CO2, and was 0.62 mmol/（m^2 · d） in the outside part of the bay, a weak source of atmospheric CO2. The average air-sea flux of CO2 in the Prydz Bay was 2.50 mmol/（m^2 · d）.     

Regional estimates of POC export flux derived from thorium-234 in the western Arctic Ocean

1Introduction CarboncyclingintheArcticOceanplaysanim- portantroletoglobalchange.Traditionally,marine productivityintheArcticOceanisthoughttobevery low,andthussomebiogeochemicalprocessessuchas particleexportandcyclingofnutrientsarenotsoac- tivebecauseofthembeingcoveredperenniallybyice, lowtemperatureandshorttimeofphotosynthesis (PlattandRao,1975).Afewpreviousestimatesof particulateorganiccarbon(POC)exportindicateda neglectablemagnitudeinthecentralArcticOcean (Baconetal.,1989).However,recen…     

234Th/238U disequilibrium and particulate organic carbon export in the northwestern South China Sea

234 Th was utilized as a tracer of particulate organic carbon (POC) export in the northwestern South China Sea (SCS) on the basis of the data collected at four stations during a spring cruise.Depth profiles of dissolved and particulate 234 Th activities were measured in the upper 60 m,showing a significant deficit relative to 238 U over the investigated stations.A stratified structure of 234 Th-238 U disequilibrium was in general observed in the upper 60 m water column,indicating that the euphotic zone of t...     

Particulate organic carbon export flux by 234Th/238U disequilibrium in the continental slope of the East China Sea

234Th is widely used to quantify the magnitude of upper ocean particulate organic carbon(POC)export in oceans.In the present work,the rates of particulate organic carbon export were measured based on the distribution patterns of234Th/238U disequilibrium in the water column within the continental slope of the East China Sea(ECS)during May 2011.The profiles of particulate and dissolved234Th activities at all three stations showed a relative deficit with respect to238U in the upper 100 m of the water column.The dissolved234Th scavenging rates and the particulate234Th removal rates and their residence times were calculated by a one-dimensional steady state model.The results showed that the dissolved234Th scavenging rates and the particulate234Th removal rates ranged from 12.4–61.4 dpm/(m3·d)andfrom3.8–21.8 dpm/(m3·d),respectively.The residence times of dissolved and particulate234Th were in the range of 3.4–158 d and 63.7–96.5 d,respectively.Combined with the measurement of POC/234Th ratios of suspended particles,POC export flux(calculated by carbon)from the euphotic zone was estimated in the study region,which ranged from 4.14–14.7 mmol/(m2·d),withanaverageof8.21mmol/(m2·d),occupying35%oftheprimeproductivity in the study area.The results of this study can provide new information for better understanding the carbon biogeochemical cycle within the continental slope of the ECS.     

Size-fractionated uranium isotopes in surface waters in the Jiulong Estuary in China

Surface water was collected from the Jiulong Estuary for determination of activity concentrations of uranium isotopes in different size fractions, namely, greater than 53, 10 -53, 2 - 10, 0.4 -2 μm, 10 000 u -0.4 μm and less than 10 000 u fractions by microfihration and cross-flow uhrafiltration technologies. Results indicated that most of the dissolved uranium （ 〈 0.4 μm） exis- ted in the low molecular mass fraction （ 〈 10 000 u）, and the colloidal uranium-238 （10 000 u -0.4 μm） only contributed less than 1% of the dissolved uranium-238. The fractions of colloidal uranium in the dissolved phases decreased with the increasing sa- linity. A positive linear relationship between uranium-238 activities and salinities was observed for the dissolved, colloidal and low molecular mass fractions, indicating a conservative behavior of uranium in the Jiulong Estuary. In the particulate phases （ 〉 0.4 μm）, the partitioning of uranium isotopes among different size fractions was controlled by the partitioning of particle concentrations. In the regions with salinities below 20, the partitioning of uranium-238 among different size fractions was as follows： 10 - 53 μm 〉 2 - 10 μm 〉 0.4 - 2 μm greater than above 53 μm. However, the order at the offshore station with salinities above 30 changed as follows ： 0.4 - 2 μm 〉 10 - 53 μm 〉 2 - 10 μm greater than above 53 μm. The fraction of the 0.4 - 2 μm particles increased at the offshore station, suggesting the increased contribution of the authigenic uranium. The activity ratio of uranium-234 to uranium-238 in the dissolved phases, including the low molecular mass fraction and the colloidal fraction, was larger than unity, showing the occurrence of excess uranium-234. In contrast, the activity ratio of uranium-234 to uranium-238 in all size fractions of the particulate phase was close to the equilibrium value （1.0）. The observed different values of the activity ratio of uranium-234 to uranium-238 in the dissolved phase and the partic     

Utilizing ~(234)Th/~(238)U disequilibrium to constrain particle dynamics in hydrothermal plumes in the Southwest Indian Ocean

Metal-enriched minerals have been widely observed near hydrothermal vent fields.However,the dynamics of particulate metals influenced by hydrothermal activities is poorly constrained.Here,radioactive ~(234)Th in both dissolved and particulate phases were used to examine the kinetics of particle-reactive metal adsorption,removal,and residence in a newly found hydrothermal plume over the Southwest Indian Ridge.The results showed a relatively low value on ~(234)Th/~(238)U ratios(i.e.,0.73-0.88) compared to the deep oceans,indicating an enhanced adsorption of particle-reactive metals onto particulate matter in the plume.Based on the ~(234)Th-~(238)U disequilibria,the adsorption and sinking rate constants of ~(234)Th averaged(0.009±0.001) d~(-1) and(0.113±0.024) d~(-1) in the hydrothermal plume,corresponding to the residence times of(115±19) d and(16±5) d for dissolved and particulate ~(234)Th,respectively.This timescale allows vent-discharged particle-reactive metals to disperse hundreds to thousands of miles away.Thus,hydrothermal activities might influence the metal distribution in deep ocean over a very large scope.Also,a high sinking flux of(36.2±5.4) B q/(m~2·d) for ~(234)Th was observed for the plume,suggesting an enrichment of metal in particles deposited close to the vent.The enhancement of particle sinking could also benefit the transport of organic carbon and nitrogen and fuel the benthic ecosystems under the plume regimes.Thus,hydrothermal plumes may have an impact on both the elemental geochemistry and/or ecosystem to the deep oceans interior than previous expectation.     

西北太平洋楚科奇海沉积物-水界面营养盐输送通量估算

陆架区沉积物间隙水的营养盐再生是水体营养盐补充的重要途径之一。楚科奇海陆架区中部沉积物间隙水中的营养盐分布,是物理和生物扰动较弱状态下的沉积物-水界面的典型分布。本文对中国第4次北极科学考察采集的4个多管短柱沉积物样品及多管样站位的上层水样进行分析,得到沉积物间隙水、上覆水以及水柱中营养盐数据。结果表明,沉积物间隙水各营养盐浓度均先随沉积深度增加而呈指数快速升高,记为Ⅰ层;然后进入沉积物再矿化作用与营养盐移出速率相互抵消的稳定变化层,营养盐浓度在该阶段基本不变,记为Ⅱ层;最后是营养盐缓慢递减层,记为Ⅲ层,由于该层有机质降解作用耗尽氧气,NO-3和PO3-4被还原细菌利用而失去氧离子。通过双层模式和Fick第一扩散定律,计算得出楚科奇海沉积物-水界面硅酸盐、磷酸盐和硝酸盐的扩散通量分别为1.660mmol/(m2·d)(以Si计量)、0.008mmol/(m2·d)(以P计量)、0.117mmol/(m2·d)(以N计量)(以R06站为例)。四个调查站位沉积物中硅酸盐的扩散通量分别为3.101mmol/(m2·d)(以Si计量,CC1站)、1.660mmol/(m2·d)(以Si计量,R06站)、1.307mmol/(m2·d)(以Si计量,C07站)、0.243mmol/(m2·d)(以Si计量,S23站),含量呈现明显的纬度分布特征。沉积物间隙水N*的分布表明,楚科奇海沉积环境具有很强的反硝化过程,沉积物脱氮作用是硝酸盐一个重要的汇。     

Upper ocean export of particulate organic carbon and biogenic silica in the Southern Ocean along 170°W

Upper-ocean fluxes of particulate organic carbon (POC) and biogenic silica (bSi) are calculated from four US JGOFS cruises along 170°W using a thorium-234 based approach. Both POC and bSi fluxes exhibit large variability vs. latitude during the seasonal progression of diatom dominated blooms. POC fluxes at 100 m of up to 50 mmol C m⁻² d⁻¹ are found late in the bloom, and farthest south near the Ross Sea Gyre. Biogenic Si fluxes also peak late in the bloom as high as 15 mmol Si m⁻² d⁻¹, but this flux peak occurs at a different latitude, just south of the Antarctic Polar Front (APF), which is centered around 60°S along this cruise track. The ratios of both POC and bSi export relative to their production rates are large, suggesting an efficient biological pump at these latitudes. The highest relative bSi/POC flux ratios at 100 m are found just south of the APF, coincident with a bSi/POC flux peak seen in 1000 m traps during this same program by Deep-Sea Research II (Honjo et al., Deep-Sea Research II 47, 3521–3548). These data suggest that efficient export at these latitudes can support the high accumulation rates of bSi found in the sediments under and south of the APF, despite the generally low biomass and productivity levels in this region.     

Influence of particle composition on thorium scavenging in the marginal China seas

Thorium-234 and particle composition (organic matter, biogenic silica, carbonate and lithogenic component) were examined in the East China Sea (ECS) and the northern South China Sea (NSCS) in order to constrain the particle types scavenging thorium isotopes. Good positive correlations between particulate organic matter (POM) or carbonate and thorium-234 in suspended particulate matter (SPM) indicates that POM and carbonate are efficient to scavenge thorium-234. No relationship between biogenic silica and thorium-234 suggests that geochemical behavior of thorium-234 may be not influenced by biogenic silica. A simple model was used to evaluate the affinity of thorium-234 to different particle components. The results show that POM is the most efficient scavenger for thorium-234 in the ECS and the NSCS, followed by carbonate. The authors'' results lend support to the utility of thorium-234 as a proxy of POC and carbonate in the upper layer. However, the strong dependence of thorium scavenging on particle composition challenges thorium-230 as a constant flux proxy.     

Sediment trap experiments in the water column off southwestern Taiwan:234Th fluxes

The activity of²³⁴Th (t _1/2=24.1 days) in dissolved, particulate and sediment trap samples was determined in the water column off southwestern Taiwan during 2–4 October, 1993. Vertical²³⁴Th fluxes measured by the free-floating sediment traps ranged from 363 to 2290 dpm m^–2 d^–1 in the upper 450 m. Th-234 fluxes predicted from the irreversible scavenging model concur with those measured by the sediment traps. Comparison of the residence times of particulate²³⁴Th and particulate organic carbon showed that their respective values differ by a factor of approximately 23, which suggests organic carbon is preferentially recycled relative to²³⁴Th in the euphotic zone.     

厦门湾水体中颗粒有机碳的垂向输出通量:234Th/238U不平衡的应用

对厦门湾塔角附近海域某站位叶绿素 a、POC、初级生产力、234Th/238U不平衡进行的周日变化研究表明,POC含量介于14.4～34.6 mmol/m3之间,其中碎屑有机碳与活体有机碳所占份额分别为74%～92%和8%～26%.POC垂直分布呈现由表及底降低的趋势,且白昼期间POC含量高于晚间,说明研究海域POC含量与生物过程具有密切联系.初级生产力水平在1d之中变化达5倍,垂直分布亦随深度增加而降低,与叶绿素a的变化相对应.短时间(2h)培养获得的初级生产力水平明显高于长时间培养(24 h)的结果,证实部分新固定的碳被优先呼吸排出.结合234Th/238U不平衡法获得的颗粒态234Th输出通量及输出界面颗粒物中的POC/P_Th比值,可计算出真光层 POC的垂向输出通量为16.0mmol/(m2·d),其中碎屑有机碳与活体有机碳贡献的数量分别为13.3和2.7mmol/(m2·d).POC输出通量与初级生产力的比值(ThE比值)平均为0.31,真光层POC停留时间平均为11d.上述结果与Aksnes和Wassmann[1]的模型计算结果相吻合,但与其他大多数模型的结果仍存在一定的差异.     

Using triple oxygen isotopes and oxygen-argon ratio to quantify ecosystem production in the mixed layer of northern South China Sea slope region

Quantifying the gross and net production is an essential component of carbon cycling and marine ecosystem studies.Triple oxygen isotope measurements and the O_2/Ar ratio are powerful indices in quantifying the gross primary production and net community production of the mixed layer zone,respectively.Although there is a substantial advantage in refining the gas exchange term and water column vertical mixing calibration,application of mixed layer depth history to the gas exchange term and its contribution to reducing indices error are unclear.Therefore,two cruises were conducted in the slope regions of the northern South China Sea in October 2014(autumn) and June 2015(spring).Discrete water samples at Station L07 in the upper 150 m depth were collected for the determination of δ~(17)0,δ~(18)O,and the O_2/Ar ratio of dissolved gases.Gross oxygen production(GOP) was estimated using the triple oxygen isotopes of the dissolved O_2,and net oxygen production(NOP) was calculated using O_2/Ar ratio and O_2 concentration.The vertical mixing effect in NOP was calibrated via a N_2O based approach.GOP for autumn and spring was(169±23) mmol/(m~2·d)(by O_2) and(189±26) mmol/(m~2·d)(by O_2),respectively.While NOP was 1.5 mmol/(m~2·d)(by O_2) in autumn and 8.2 mmol/(m~2·d)(by O_2) in spring.Application of mixed layer depth history in the gas flux parametrization reduced up to 9.5% error in the GOP and NOP estimations.A comparison with an independent O_2 budget calculation in the diel observation indicated a26% overestimation in the current GOP,likely due to the vertical mixing effect.Both GOP and NOP in June were higher than those in October.Potential explanations for this include the occurrence of an eddy process in June,which may have exerted a submesoscale upwelling at the sampling station,and also the markedly higher terrestrial impact in June.     

长江口邻近海域透明胞外聚合颗粒物浓度和沉降速率研究

透明胞外聚合颗粒物（Transparent exopolymer particles，TEPs）在海洋中分布广泛，其沉降被认为是海洋中生物碳沉降的途径之一。本研究于2011年春季和夏季调查了长江口邻近海域TEPs的浓度和沉降速率，并且估算了其碳沉降通量。研究发现，TEPs浓度春季介于40.00~1040.00 μg Xeq L^-1，平均值为209.70±240.93 μg Xeq L^-1；夏季介于56.67~1423.33 μg Xeq L^-1，平均值为433.33±393.02 μg Xeq L^-1。两个季节，TEPs在水华站位的浓度明显高于非水华站位。相关性分析表明，TEPs与水体叶绿素a浓度呈显著正相关性，表明在调查区浮游植物是TEPs的主要生产者。TEPs沉降速率在春季介于0.08~0.57 m d^-1，平均值为0.28±0.14 m d^-1；夏季介于0.10~1.08 m d^-1，平均值为0.34±0.31 m d^-1。经估算，TEPs碳沉降通量春季介于4.95~29.40 mg C m^-2 d^-1，平均值为14.66±8.83 mg C m^-2 d^-1；夏季介于6.80~30.45 mg C m^-2 d^-1，平均值为15.71±8.73 mg C m^-2 d^-1。TEPs的碳沉降通量可以占到浮游植物碳沉降通量的17.81%~138.27%。水华站位TEPs的碳沉降通量明显高于非水华站位，这是由于水华站位较高的TEPs浓度及沉降速率所致。本研究表明，TEPs的沉降在长江口邻近海域是碳沉降的有效途径，在相应的碳沉降相关研究中应该被考虑进来。     

Role of colloidal material in the removal of 234Th in the Canada basin of the Arctic Ocean

The phase partitioning of ²³⁴Th between dissolved (<10-kiloDalton, kD), colloidal (10 kD—0.4 μm), and particulate (⩾0.5 μm) matter across a horizontal transect, from a coastal station to the deep Canada Basin, and a vertical profile in the deep Canada Basin of the western Arctic Ocean was investigated. Concentrations of suspended particulate matter (SPM), dissolved, colloidal and particulate organic carbon, particulate organic nitrogen and nutrients (silicate, phosphate and nitrate) were also measured to assess transport and scavenging processes.Total ²³⁴Th (colloidal+particulate+dissolved) indicated deficiencies relative to secular equilibrium with its parent, ²³⁸U in the upper 100 m, which suggests active scavenging of ²³⁴Th onto particle surfaces. In contrast, at depths >200 m, general equilibrium existed between total ²³⁴Th and ²³⁸U. The inventory of SPM and the specific activity of particulate ²³⁴Th in the Canada Basin was about an order of magnitude higher than the profile reported for the Alpha Ridge ice camp station. This higher concentration of SPM in the southwestern Canada Basin is likely derived from ice-rafted sedimentary particles. Inventories of nutrients, and dissolved organic carbon and nitrogen in the upper 100 m of the Canada Basin are comparable to the other estimates for the central Arctic Ocean. Comparison of the mass concentrations of colloidal and filter-retained particulate matter as well as the activity of ²³⁴Th in these phases indicates that only a very small component of the colloidal material is actively involved in Th scavenging. Lower values of the conditional partition coefficient between the colloidal and dissolved phase indicate that the Arctic colloids are less reactive than colloidal material from other regions. The conditional partition coefficient between the filter-retained and dissolved phases (K_f) is generally higher than that for other regions, which is attributed to the higher complexation capacity of glacio-marine sedimentary particles in these waters. The ²³⁴Th-derived export of POC for the shelf and deep Canada Basin ranges between 5.6 and 6.5 mmol m⁻² d⁻¹, and is in agreement with other estimates reported for the central Arctic Ocean and Beaufort Sea.     

The particle fluxes in sediment traps from Niulang Guyot area in the Northwest Pacific Ocean

The flux of settling particles in the ocean has been widely explored since 1980s due to its important role in biogenic elements cycling, especially in the transport of particulate organic carbon (POC) in the deep sea. However, research in the seamount area of the oligotrophic subtropical Northwest Pacific Ocean is lacking. In this work, two sediment traps were deployed at the foot and another two at the hillside of Niulang Guyot from August 2017 to July 2018. The magnitude and composition of particle fluxes were measured. The main factors influencing the spatial variations of the fluxes were evaluated. Our results indicated a low particulate flux from Niulang Guyot area in the Northwest Pacific Ocean, reflecting low primary productivity of the oligotrophic ocean. The total mass flux (TMF) decreased from 2.57 g/(m2·a) to 0.56 g/(m2·a) with increasing depth from 600 m to 4 850 m. A clear seasonal pattern of TMF was observed, with higher flux in summer than that in winter. The peak flux of 26.52 mg/(m2·d) occurred in August at 600 m, while the lowest value of 0.07 mg/(m2·d) was shown in February at 4 850 m. The settling particles at the deep layers had similar biochemical composition, with calcium carbonate (CaCO₃) accounting for up to 90%, followed by organic matter and opal, characteristics of Carbonate Ocean. The POC flux decreased more rapidly in the twilight layer because of faster decomposition, remineralization, and higher temperature. A small fraction of POC was transported into the deep ocean by biological pump. Particle fluxes were mainly controlled by the calcareous ballasts besides the primary productivity of the surface water. The advection may be another important factor affecting the flux in the seamount area. The combination of settled matters rich in foraminiferal tests with topography and currents may be the reason for regulating the local abundance of benthos on seamounts. Our results will fill in the knowledge gap of sedimentation flux, improve the understanding of ecosystem in Niulang Guyot area, and eventually provide data support for the optimization of regional ecological modeling.     

南沙海域上层海水碳垂直通量的初步研究

根据１９９０年５－６月在南沙海域４个站点投放颗粒物捕集器采集样品的分析结果，计算了该海域上层海水碳垂直通量。结果表明：（１）南沙海域上层海水颗粒有机碳总生成量为２９８ｍｇ／（ｍ＾２．ｄ），其中３５％分解参与再循环，６５％以颗粒形式离开真光层向下输送；（２）颗粒有机碳向下通量为１９３ｍｇ／（ｍ＾２．ｄ）。总溶解无机碳穿过跃层向上垂直通量为３６００ｍｇ／（ｍ＾２．ｄ），真光层颗粒无机碳向下通量为２７ｍ     

Responses of nutrient biogeochemistry and nitrogen cycle to seasonal upwelling in coastal waters of the eastern Hainan Island

The coastal upwelling has profound influence on the surrounding ecosystem by supplying the nutrient-replete water to the euphotic zone. Nutrient biogeochemistry was investigated in coastal waters of the eastern Hainan Island in summer 2015 and autumn 2016. From perspectives of nutrient dynamics and physical transport, the nutrient fluxes entered the upper 50 m water depth（between the mixed layer and the euphotic zone） arisen from the upwelling were estimated to be 2.5-5.4 mmol/（m²·d）,...