Seasonal variations in dissolved organic carbon concentrations and characteristics in a shallow coastal bay

Dissolved organic matter (DOM) composition and dynamics in temperate shallow coastal bays are not well described although these bays may be important as local sources of organic carbon to ocean waters and are often sites of economically-important fisheries and aquaculture. In this study surface water samples were collected on a monthly to bi-monthly basis over two years from a mid-Atlantic coastal bay (Chincoteague Bay, Virginia and Maryland, USA). Dissolved organic carbon (DOC) concentrations and light absorbance characteristics were measured on sterile-filtered water, and high-molecular weight (> 1 kDa) dissolved OM (DOM) was isolated to determine stable isotope composition and molecular-level characteristics. Our time series encompassed both a drought year (2002) and a year of above-average rainfall (2003). During the dry year, one of our sites developed a very intense bloom of the brown tide organism Aureococcus anophagefferens while during the wet year there were brown tide bloom events at both of our sampling sites. During early spring of the wet year, there were higher concentrations of > 1 kDa DOC; this fraction represented a larger proportion of overall DOC and appeared considerably more allochthonous. Based upon colored dissolved organic matter (CDOM) and high-molecular weight DOM analyses, the development of extensive phytoplankton blooms during our sampling period significantly altered the quality of the DOM. Throughout both years Chincoteague Bay had high DOC concentrations relative to values reported for the coastal ocean. This observation, in conjunction with the observed effects of phytoplankton blooms on DOM composition, indicates that Chincoteague Bay may be a significant local source of “recently-fixed” organic carbon to shelf waters. Estimating inputs of DOC from Chincoteague Bay to the Mid-Atlantic Bight suggests that shallow productive bays should be considered in studies of organic carbon on continental shelves.     

Sources and transport of dissolved and particulate organic carbon in the Mississippi River estuary and adjacent coastal waters of the northern Gulf of Mexico

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.     

长江口表层沉积物中正构烷烃的高分辨分布特征及有机碳来源解析

于2014年3月对长江口及邻近海域的表层沉积物进行了高分辨率采样,分析了沉积物粒级组成、比表面积、总有机碳含量及其稳定碳同位素组成(δ¹³C)、正构烷烃及其相关分子指标,讨论了此区域沉积有机碳和正构烷烃的高分辨分布特征,并结合基于主成分分析-蒙特卡洛模拟的三端元混合模型,对沉积有机碳的来源进行了定量解析。结果表明,长江口及其邻近海域表层沉积物中总有机碳含量为0.45%±0.16%,近岸泥质区总有机碳含量较高,外海砂质区含量较低。总正构烷烃(C₁₄-C₃₅)的绝对含量和相对于总有机碳的含量分别为(1.42±0.73)μg/g和(0.34±0.21) mg/g。泥质区以长链正构烷烃占优势,具有较强的奇碳优势;砂质区以短链正构烷烃占优势,且具有一定的偶碳优势。长江输入、老黄河口输入、闽浙沿岸小型河流输入和水动力分选等因素制约了正构烷烃的输运和分布特征。模型结果显示此区域沉积有机碳来自海源、土壤和高等植物的混合输入,其中以海源为主,其贡献为42.70%±18.18%,由陆地向外海贡献逐渐升高,其次是土壤和高等植物,其贡献分别为2...     

夏季珠江口邻近海域表层浮游植物的碳叶绿素比值及其碳含量

Chlorophyll a(Chl a),particulate organic carbon(POC)and biogenic silica(BSi)were determined in coastal waters adjacent to the Zhujiang(Pearl)River Estuary(ZRE)during summer,in order to examine the C:Chl a ratio of phytoplankton and phytoplankton carbon in the plume-impacted coastal waters during summer,as well as to assess the relative contribution of diatoms to the phytoplankton biomass,by the regression between Chl a,POC and BSi.Our results showed that the C:Chl a ratio(g/g)of phytoplankton was high(up to 142),likely due to high light intensity and nutrient limitation.The river plume input stimulated phytoplankton growth,especially diatoms,resulting in higher relative contribution of phytoplankton carbon(55%)and diatoms(34%)to POC in the plume-impacted region than those(33%and 13%)in high salinity area,respectively.Phytoplankton carbon(up to 538μg/L)in the plume-impacted region was much higher than that(<166μg/L)in high salinity area.Our findings were helpful to improve the biogeochemical model in coastal waters adjacent to the ZRE.     

Grain size composition and transport of sedimentary organic carbon in the Changjiang River (Yangtze River) Estuary and Hangzhou Bay and their adjacent waters

Surface sediments from the Changjiang River(Yangtze River) Estuary,Hangzhou Bay,and their adjacent waters were analyzed for their grain size distribution,organic carbon(OC) concentration,and stable carbon isotope composition(δ13C).Based on this analysis,about 36 surface sediment samples were selected from various environments and separated into sand(0.250 mm,0.125–0.250 mm,0.063–0.125 mm) and silt(0.025–0.063 mm)fractions by wet-sieving fractionation methods,and further into silt-(0.004–0.025 mm) and clay-sized(0.004mm) fractions by centrifugal fractionation.Sediments of six grain size categories were analyzed for their OC andδ13C contents to explore the grain size composition and transport paths of sedimentary OC in the study area.From fine to coarse fractions,the OC content was 1.18%,0.51%,0.46%,0.42%,0.99%,and 0.48%,respectively,while theδ13C was –21.64‰,–22.03‰,–22.52‰,–22.46‰,–22.36‰,and –22.28‰,respectively.In each size category,the OC contribution was 42.96%,26.06%,9.82%,5.75%,7.09%,and 8.33%,respectively.The OC content in clay and fine silt fractions(0.025 mm) was about 69.02%.High OC concentrations were mainly found in offshore modern sediments in the northeast of the Changjiang River Estuary,in modern sediments in the lower estuary of the Changjiang River and Hangzhou Bay,and in Cyclonic Eddy modern sediments to the southwest of the Cheju Island.Integrating the distribution of terrestrial OC content of each grain size category with the δ13C of the bulk sediment indicated that the terrestrial organic material in the Changjiang River Estuary was transported seaward and dispersed to the Cyclonic Eddy modern sediments to the southwest of the Cheju Island via two pathways:one was a result of the Changjiang River Diluted Water(CDW) northeastward extending branch driven by the North Jiangsu Coastal Current and the Yellow Sea Coastal Current,while the other one was the result of the CDW southward extending branch driven by the Taiwan Warm Current.     

The cycling and oxidation pathways of organic carbon in a shallow estuary along the Texas Gulf Coast

The cycling and oxidation pathways of organic carbon were investigated at a single shallow water estuarine site in Trinity Bay, Texas, the uppermost lobe of Galveston Bay, during November 2000. Radio-isotopes were used to estimate sediment mixing and accumulation rates, and benthic chamber and pore water measurements were used to determine sediment-water exchange fluxes of oxygen, nutrients and metals, and infer carbon oxidation rates. Using ⁷Be and ²³⁴Th_XS, the sediment-mixing coefficient (D_b) was 4.3 ± 1.8 cm² y⁻¹, a value that lies at the lower limit for marine environments, indicating that mixing was not important in these sediments at this time. Sediment accumulation rates (S_a), estimated using ¹³⁷Cs and ²¹⁰Pb_XS, were 0.16 ± 0.02 g cm⁻² y⁻¹. The supply rate of organic carbon to the sediment-water interface was 30 ± 3.9 mmol C m⁻² d⁻¹, of which ∼10% or 2.9 ± 0.44 mmol C m⁻² d⁻¹was lost from the system through burial below the 1-cm thick surface mixed layer. Measured fluxes of O₂ were 26 ± 3.8 mmol m⁻² d⁻¹ and equated to a carbon oxidation rate of 20 ± 3.3 mmol C m⁻² d⁻¹, which is an upper limit due to the potential for oxidation of additional reduced species. Using organic carbon gradients in the surface mixed layer, carbon oxidation was estimated at 2.6 ± 1.1 mmol C m⁻² d⁻¹. Independent estimates made using pore water concentration gradients of ammonium and C:N stoichiometry, equaled 2.8 ± 0.46 mmol C m⁻² d⁻¹. The flux of DOC out of the sediments (DOC_efflux) was 5.6 ± 1.3 mmol C m⁻² d⁻¹. In general, while mass balance was achieved indicating the sediments were at steady state during this time, changes in environmental conditions within the bay and the surrounding area, mean this conclusion might not always hold. These results show that the majority of carbon oxidation occurred at the sediment-water interface, via O₂ reduction. This likely results from the high frequency of sediment resuspension events combined with the shallow sediment mixing zone, leaving anaerobic oxidants responsible for only ∼10–15% of the carbon oxidized in these sediments.     

浒苔绿潮暴发期间海水溶解有机碳的生物可利用性及其碳汇作用

自2007年以来,浒苔绿潮已经连续15年在南黄海暴发。浒苔(Ulva prolifera)作为主要肇事藻种,在暴发过程中向海水释放大量的溶解有机碳(DOC)。然而,这些藻源DOC能否长期保存在海洋中,主要取决于它们的生物可利用性,目前关于此方面的研究甚少。本研究在浒苔绿潮大规模暴发时期(2019年6月),分别在浒苔暴发海区和无浒苔海区各选择3个站位富集表层海水,在实验室进行长期(300 d)的DOC降解实验。结果发现,在60 d内,不同站位富集海水中的DOC浓度随着微生物的利用快速下降,微生物丰度也在第60天达到峰值,表明这些被消耗的DOC是生物可利用性高的活性DOC(LDOC)。60 d后,剩余的DOC可抵抗微生物的降解,在60～300 d内保持稳定,表明这些DOC是具有强稳定性的惰性DOC(RDOC)。最终发现,浒苔暴发海水的RDOC占富集DOC的46%,明显高于无浒苔海水的(36%)。并且,荧光溶解有机物(FDOM)中活性的类蛋白组分随着微生物的利用被快速消耗,惰性的类腐殖质组分逐渐积累,暗示了在降解过程中LDOC逐渐向RDOC转化。可见,浒苔绿潮暴发除了在短时间内增加海水中的D...     

Burial fluxes and source apportionment of carbon in culture areas of Sanggou Bay over the past 200 years

In this study,we assessed the burial fluxes and source appointment of different forms of carbon in core sediments collected from culture areas in the Sanggou Bay,and preliminarily analyzed the reasons for the greater proportion of inorganic carbon burial fluxes(BFTIC).The average content of total carbon(TC) in the Sanggou Bay was 2.14%.Total organic carbon(TOC) accounted for a small proportion in TC,more than 65% of which derived from terrigenous organic carbon(Ct),and while the proportion of marine-derived organic carbon(Ca) increased significantly since the beginning of large-scale aquaculture.Total inorganic carbon(TIC) accounted for 60%–75%of TC,an average of which was 60%,with a maximum up to 90% during flourishing periods(1880–1948) of small natural shellfish derived from seashells inorganic carbon(Shell-IC).The TC burial fluxes ranged from 31 g/(m2·a)to 895 g/(m2·a) with an average of 227 g/(m2·a),which was dominated by TIC(about 70%).Shell-IC was the main source of TIC and even TC.As the main food of natural shellfish,biogenic silica(BSi) negatively correlated with BFTIC through affecting shellfish breeding.BFTIC of Sta.S1,influenced greatly by the Yellow Sea Coastal Current,had a certain response to Pacific Decadal Oscillation(PDO) in some specific periods.     

Dynamics and sources of suspended particulate organic matter in the Marennes-Oléron oyster farming bay: Insights from stable isotopes and microalgae ecology

The aim of this study was to distinguish between sources of the complex variety of Marennes-Oléron Bay suspended particulate organic matter (SPOM) contributing to the tropho-dynamics of the Marennes-Oléron oyster farming bay. Basic biomarkers (Chl a, C/N and POC/Chl a ratios), carbon and nitrogen stable isotopes from SPOM were analyzed and the microalgae community was characterized. The sampling strategy was bimonthly from March 2002 to December 2003; samples were taken from an intertidal mudflat. Four main sources contributed to the SPOM pool: terrigenous input from rivers, neritic phytoplankton, resuspended microphytobenthos and periodic inputs from intertidal Zostera noltii meadows. Seasonal fluctuations were observed in both years of the study period: (1) SPOM collected in the spring of 2002 (δ¹³C = −25‰ to −23‰) was mainly composed of fresh estuarine inputs; (2) SPOM from the summer and fall of 2002 and 2003 was predominantly neritic phytoplankton (δ¹³C = − 22‰ to −19‰); (3) SPOM from the winter of 2002, spring of 2003 and winter of 2003 (δ¹³C = −21 to −23‰) was composed of a mixture of decayed terrigenous river inputs and pelagic phytoplankton, which was predominantly resuspended microphytobenthos. In the summer of 2003—the warmest summer on record in southern France and Europe—SPOM was particularly enriched for ¹³C, with δ¹³C values ranging from −14‰ to −12‰. Pulses in δ¹³C values, indicative of ¹³C-enriched decaying materials, extended into the fall. These were attributed to benthic intertidal inputs, including both resuspended microphytobenthos and Z. noltii detritus. Changes in SPOM sources in Marennes-Oléron Bay may lead to differences in the quality of the trophic environment available for reared oysters.     

Effects of upwelling,tides and biological processes on the inorganic carbon system of a coastal lagoon in Baja California

The role of coastal lagoons and estuaries as sources or sinks of inorganic carbon in upwelling areas has not been fully understood. During the months of May–July, 2005, we studied the dissolved inorganic carbon system in a coastal lagoon of northwestern Mexico during the strongest period of upwelling events. Along the bay, different scenarios were observed for the distributions of pH, dissolved inorganic carbon (DIC) and apparent oxygen utilization (AOU) as a result of different combinations of upwelling intensity and tidal amplitude. DIC concentrations in the outer part of the bay were controlled by mixing processes. At the inner part of the bay DIC was as low as 1800 μmol kg⁻¹, most likely due to high water residence times and seagrass CO₂ uptake. It is estimated that 85% of San Quintín Bay, at the oceanic end, acted as a source of CO₂ to the atmosphere due to the inflow of CO₂-rich upwelled waters from the neighboring ocean with high positive fluxes higher than 30 mmol C m⁻² d⁻¹. In contrast, there was a net uptake of CO₂ and HCO₃⁻ by the seagrass bed Zostera marina in the inner part of the bay, so the pCO₂ in this zone was below the equilibrium value and slightly negative CO₂ fluxes of −6 mmol C m⁻² d⁻¹. Our positive NEP and ΔDIC values indicate that Bahía San Quintín was a net autotrophic system during the upwelling season during 2005.     

Nutrient Dynamics in Vegetated and Unvegetated Areas of a Southern Everglades Mangrove Creek

Flow-through flumes were used to quantify net areal fluxes of nutrients in the fringe mangrove zone of lower Taylor River in the southern Everglades National Park. We also quantified net areal fluxes along the open water portion of the channel to determine the relative importance of either zone (vegetated vs. unvegetated) in the regulation of nutrient exchange in this system. Taylor River's hydrology is driven mainly by precipitation and wind, as there is little influence of tide. Therefore, quarterly samplings of the vegetated and unvegetated flumes were slated to include typical wet season and dry season periods, as well as between seasons, over a duration of two years. Concentrations of dissolved and total organic carbon (DOC and TOC) were highest during the wet season and similar to one another throughout the study, reflecting the low particulate loads in this creek. Dissolved inorganic nitrogen (nitrate+nitrite+ammonium) was 10–15% of the total nitrogen (TN) content, with NO−x and NH+4 showing similar concentration ranges over the 2-year study. Soluble reactive phosphorus (SRP) was usually <0·05μM, while total phosphorus (TP) was typically an order of magnitude higher. Net areal fluxes were calculated from nutrient concentration change over the length of the flumes. Most flux occurred in the vegetated zone. Dissolved inorganic nitrogen and DOC were usually taken up from the water column; however, we saw no seasonal pattern for any constituent over the course of this study. Total nutrients (TOC, TN, and TP) showed little net exchange and, like SRP, had fluxes that shifted irregularly throughout the study. Despite the lack of a clear seasonal pattern, there was a great deal of consistency between vegetated flumes, especially for NO−x and NH+4, and fluxes in the vegetated flumes were generally in the same direction (import, export, or no net flux) during a given sampling. These findings suggest that the fringe mangrove zone is of considerable importance in regulating nutrient dynamics in lower Taylor River. Furthermore, the influence of this zone may at times extend into northeast Florida Bay, as the bay is the primary recipient of water and nutrients during the wet season.