Influence of Mussel Culture on the Vertical Export of Phytoplankton Carbon in a Coastal Upwelling Embayment (Ría de Vigo,NW Iberia)

The goal of this paper is to find out whether suspended mussel culture affects the vertical fluxes of biogenic particles in the Ría de Vigo on a seasonal scale. With this aim, vertical fluxes of particulate organic carbon (POC) and the magnitude and composition of vertical export of phytoplankton carbon (Cphyto) collected in sediment traps were examined by comparing data obtained inside a mussel farming area (RaS) with those found at a reference station (ReS) not affected by mussels. Our results indicate that mussel farming has a strong impact on sedimentation fluxes under the rafts, not only increasing POC flux but also altering the magnitude and composition of Cphyto fluxes. Average POC flux at RaS (2564?±?1936 mg m^?2 day^?1) was four times higher than at ReS (731?±?276 mg m^?2 day^?1), and much of this increase was due to biodeposit fluxes (Cbiodep) which accounted for large proportion of POC flux (35–60 %). Indeed, because of this high Cbiodep flux, only a small proportion of the POC flux was due to Cphyto flux (3–12 %). At the same time, we observed an increased sedimentation of phytoplankton cells at RaS that could be explained by a combination of mechanisms: less energetic hydrodynamic conditions under mussel rafts, ballast effect by sinking mussel feces, and diatom aggregates. Moreover, mussel farming also altered the quality of the Cphyto flux by removing part of the predatory pressure of zooplankton and thus matching diatom composition in water column and sediment traps.     

Decadal Change in Sediment Community Oxygen Consumption in the Abyssal Northeast Pacific

Long time-series studies are critical to assessing impacts of climate change on the marine carbon cycle. A 27-year time-series study in the abyssal northeast Pacific (Sta. M, 4000 m depth) has provided the first concurrent measurements of sinking particulate organic carbon supply (POC flux) and remineralization by the benthic community. Sediment community oxygen consumption (SCOC), an estimate of organic carbon remineralization, was measured in situ over daily to interannual periods with four different instruments. Daily averages of SCOC ranged from a low of 5.0 mg C m^?2 day^?1 in February 1991 to a high of 31.0 mg C m^?2 day^?1 in June 2012. POC flux estimated from sediment trap collections at 600 and 50 m above bottom ranged from 0.3 mg C m^?2 day^?1 in October 2013 to 32.0 mg C m^?2 day^?1 in June 2011. Monthly averages of SCOC and POC flux correlated significantly with no time lag. Over the long time series, yearly average POC flux accounted for 63 % of the estimated carbon demand of the benthic community. Long time-series studies of sediment community processes, particularly SCOC, have shown similar fluctuations with the flux of POC reaching the abyssal seafloor. SCOC quickly responds to changes in food supply and tracks POC flux. Yet, SCOC consistently exceeds POC flux as measured by sediment traps alone. The shortfall of ~37 % could be explained by sediment trap sampling artifacts over decadal scales including undersampling of large sinking particles. High-resolution measurements of SCOC are critical to developing a realistic carbon cycle model for the open ocean. Such input is essential to evaluate the impact of climate change on the oceanic carbon cycle, and the long-term influences on the sedimentation record.     

Temporal Changes in Seawater Carbonate Chemistry and Carbon Export from a Southern California Estuary

Estuaries are important subcomponents of the coastal ocean, but knowledge about the temporal and spatial variability of their carbonate chemistry, as well as their contribution to coastal and global carbon fluxes, are limited. In the present study, we measured the temporal and spatial variability of biogeochemical parameters in a saltmarsh estuary in Southern California, the San Dieguito Lagoon (SDL). We also estimated the flux of dissolved inorganic carbon (DIC) and total organic carbon (TOC) to the adjacent coastal ocean over diel and seasonal timescales. The combined net flux of DIC and TOC (F_DIC?+?TOC) to the ocean during outgoing tides ranged from ??1.8±0.5?×?10³ to 9.5±0.7?×?10³?mol C h^?1 during baseline conditions. Based on these fluxes, a rough estimate of the net annual export of DIC and TOC totaled 10±4?×?10⁶?mol C year^?1. Following a major rain event (36 mm rain in 3 days), F_DIC?+?TOC increased and reached values as high as 29.0 ±?0.7?×?10³?mol C h^?1. Assuming a hypothetical scenario of three similar storm events in a year, our annual net flux estimate more than doubled to 25 ±?4?×?10⁶?mol C year^?1. These findings highlight the importance of assessing coastal carbon fluxes on different timescales and incorporating event scale variations in these assessments. Furthermore, for most of the observations elevated levels of total alkalinity (TA) and pH were observed at the estuary mouth relative to the coastal ocean. This suggests that SDL partly buffers against acidification of adjacent coastal surface waters, although the spatial extent of this buffering is likely small.     

Change in carbon flux (1960–2015) of the Red River (Vietnam)

Global riverine carbon concentrations and fluxes have been impacted by climate and human-induced changes for many decades. This paper aims to reconstruct the longterm carbon concentrations and carbon fluxes of the Red River, a system under the coupled pressures of environmental change and human activity. Based on (1) the relationships between particulate and dissolved organic carbon (POC, DOC) or dissolved inorganic carbon (DIC), and suspended sediments (TSS) or river water discharge and on (2) the available detailed historical records of river discharge and TSS concentration, the variations of the Red River carbon concentration and flux were estimated for the period 1960–2015. The results show that total carbon flux of the Red River averaged 2555?±?639 kton C year^?1. DIC fluxes dominated total carbon fluxes, representing 64% of total, reflecting a strong weathering process from carbonate rocks in the upstream basin. Total carbon fluxes significantly decreased from 2816 kton C year^?1 during the 1960s to 1372 kton C year^?1 during the 2010s and showed clear seasonal and spatial variations. Organic carbon flux decreased in both quantity and proportion of the total carbon flux from 40.9% in 1960s to 14.9% in 2010s, reflecting the important impact of dam impoundment. DIC flux was also reduced over this period potentially as a consequence of carbonate precipitation in the irrigated, agricultural land and the reduction of the Red River water discharge toward the sea. These decreases in TSS and carbon fluxes are probably partially responsible for different negatives impacts observed in the coastal zone.     

Seasonal variability of deep ocean particle fluxes and particle composition in the north open sea of Prydz Bay

Time-series Mark VII sediment trap was deployed at 72°58.55′E, 62°28.63°S (north of the Prydz Bay, Antarctica) during the cruise of CHINARE-15 in cooperation with University of Marine of America. Seasonal variability of deep ocean particle fluxes and biogenic components were investigated in order to reveal the fluxes and biogeochemistry of sinking particles in the deep ocean. The results show that the total mass flux of sinking particles at a water depth of 1000 m ranges from 13.00 to 334.59 mg⋅d⁻¹⋅m⁻²). A marked seasonal variability exists in the fluxes of all particle components reflecting the seasonal changes in upper water productivity. Biogenic material was a significant component and biogenic silica represented more than 80% of the biogenic matter, reflecting a diatom dominated system, but a lithogenic fraction is always present. The fact that the POC dominated over particulate inorganic carbon (as CaCO₃) and C_inorg/C_org was always greater than 1, indicate a net removal of CO₂ from surface water by biological activity. __________ Translated from Acta Oceanologica Sinica, 2006, 5: 49–55 [译自:海洋 学报]     

Dissolved and particulate organic carbon in Chesapeake Bay

We measured dissolved and particulate organic carbon (DOC and POC) in samples collected along 13 transects of the salinity gradient of Chesapeake Bay. Riverine DOC and POC end-members averaged 232±19 μM and 151±53 μM, respectively, and coastal DOC and POC end-members averaged 172±19 μM and 43±6 μM, respectively. Within the chlorophyll maximum, POC accumulated to concentrations 50–150 μM above those expected from conservative mixing and it was significantly correlated with chlorophylla, indicating phytoplankton origin. POC accumulated primarily in bottom waters in spring, and primarily in surface waters in summer. Net DOC accumulation (60–120 μM) was observed within and downstream of the chlorophyll maximum, primarily during spring and summer in both surface and bottom waters, and it also appeared to be derived from phytoplankton. In the turbidity maximum, there were also net decreases in chlorophylla (?3 μg l^?1 to ?22 μg l^?1) and POC concentrations (?2 μM to ?89 μM) and transient DOC increases (9–88 μM), primarily in summer. These occurred as freshwater plankton blooms mixed with turbid, low salinity seawater, and we attribute the observed POC and DOC changes to lysis and sedimentation of freshwater plankton. DOC accumulation in both regions of Chesapeake Bay was estimated to be greater than atmospheric or terrestrial organic carbon inputs and was equivalent to ≈10% of estuarine primary production.     

CO<Subscript>2</Subscript> flux variation and its contribution area in the debris-covered area of Koxkar Glacier,Mt. Tianshan in China

During the formation and development of glacial meltwater runoff, hydrochemical erosion is abundant, especially the hydrolysis of K/Na feldspar and carbonates, which can consume H⁺ in the water, promote the formation of bicarbonate by dissolving atmospheric CO₂, and affect the regional carbon cycle. From July 21, 2015, to July 18, 2017, the CO₂ concentration and flux were observed by the eddy covariance (EC) method in the relatively flat and open moraine cover area of Koxkar Glacier in western Mt. Tianshan, China. We found that: (1) atmospheric CO₂ fluxes ranged from ??408.95 to 81.58 mmol m^?2 day^?1 (average ? 58.68 mmol m^?2 day^?1), suggesting that the study area is a significant carbon sink, (2) the CO₂ flux footprint contribution areas were primarily within 150 m of the EC station, averaging total contribution rates of 93.30%, 91.39%, and 90.17% of the CO₂ flux in the snow accumulation, snow melting, and glacial melting periods, respectively. Therefore, the contribution areas with significant influences on CO₂ flux observed at EC stations were concentrated, demonstrating that grassland CO₂ flux around the glaciers had little effect at the EC stations, (3) in the predominant wind direction, under stable daytime atmospheric stratification, the measurement of CO₂ flux, as interpreted by the Agroscope Reckenholz Tanikon footprint tool, was 79.09% ± 1.84% in the contribution area. This was slightly more than seen at night, but significantly lower than the average under unstable atmospheric stratification across the three periods of interest (89%). The average distance of the farthest point of the flux footprint under steady state atmospheric conditions was 202.61?±?69.33 m, markedly greater than that under non-steady state conditions (68.55?±?10.34 m). This also indicates that the CO₂ flux observed using EC was affected primarily by hydrochemical erosion reactions in the glacier area, (4) a good negative correlation was found between net glacier exchange (NGE) of CO₂ and air temperature on precipitation-free days. Strong ice and snow ablation could promote hydrochemical reactions of soluble substances in the debris area and accelerated sinking of atmospheric CO₂. Precipitation events might reduce snow and ice melting, driven by reduced regional temperatures. However, a connection between NGE and precipitation, when less than 8.8 mm per day, was not obvious. When precipitation was greater than 8.8 mm per day, NGE decreased with increasing precipitation, (5) graphically, the slope of NGE, related to daily runoff, followed a trend: snow melting period?>?snow accumulation period?>?early glacial ablation period?>?late glacier ablation period?>?dramatic glacier ablation period. The slope was relatively large during snow melting, likely because of CO₂ sinking caused by water–rock interactions. The chemical reaction during elution in the snow layer might also promote atmospheric CO₂ drawdown. At the same time, the damping effect of snow cover and the almost-closed glacier hydrographic channel inhibited the formation of regional runoff, possibly providing sufficient time for the chemical reaction, thus promoting further CO₂ drawdown.     

Groundwater Discharge as a Source of Dissolved Carbon and Greenhouse Gases in a Subtropical Estuary

Groundwater may be highly enriched in dissolved carbon species, but its role as a source of carbon to coastal waters is still poorly constrained. Exports of deep and shallow groundwater-derived dissolved carbon species from a small subtropical estuary (Korogoro Creek, Australia, latitude ?31.0478°, longitude 153.0649°) were quantified using a radium isotope mass balance model (²³³Ra and ²²⁴Ra, natural groundwater tracers) under two hydrological conditions. In addition, air-water exchange of carbon dioxide and methane in the estuary was estimated. The highest carbon inputs to the estuary were from deep fresh groundwater in the wet season. Most of the dissolved carbon delivered by groundwater and exported from the estuary to the coastal ocean was in the form of dissolved inorganic carbon (DIC; 687 mmol m^?2 estuary day^?1; 20 mmol m^?2 catchment day^?1, respectively), with a large export of alkalinity (23 mmol m^?2 catchment day^?1). Average water to air flux of CO₂ (869 mmol m^?2 day^?1) and CH₄ (26 mmol m^?2 day^?1) were 5- and 43-fold higher, respectively, than the average global evasion in estuaries due to the large input of CO₂- and CH₄-enriched groundwater. The groundwater discharge contribution to carbon exports from the estuary for DIC, dissolved organic carbon (DOC), alkalinity, CO₂, and CH₄ was 22, 41, 3, 75, and 100 %, respectively. The results show that CO₂ and CH₄ evasion rates from small subtropical estuaries surrounded by wetlands can be extremely high and that groundwater discharge had a major role in carbon export and evasion from the estuary and therefore should be accounted for in coastal carbon budgets.     

Cell Size-Dependent Effects of Solar UV Radiation on Primary Production in Coastal Waters of the South China Sea

In order to examine the effects of solar ultraviolet radiation (UVR, 280–400 nm) on photosynthesis of differently cell-sized phytoplankton, natural phytoplankton assemblages from the coastal waters of the South China Sea were separated into three groups (>20, 5–20, and <5 μm) and exposed to four different solar UV spectral regimes, i.e., 280–700 nm (PAR?+?UVR), 400–700 nm (PAR), 280–400 nm (UV-A?+?B), and 315–400 nm (UV-A). In situ carbon fixation measurements revealed that microplankton (>20 μm) efficiently utilized UV-A for photosynthetic carbon fixation, with assimilation number of up to 1.01 μg C (μg chl a)^?1?h^?1 under 21.4 W?m^?2 UV-A alone (about half of noontime irradiance at the surface), about 40 % higher than nanoplankton (5–20 μm). UV-B (280–315 nm) of 0.95 W?m^?2 reduced the carbon fixation by approximately 20 and 57 % in microplankton and nanoplankton assemblages, respectively. In contrast, smaller picoplankton (<5 μm) was unable to utilize UV-A for the photosynthetic carbon fixation. In addition, only micro-sized assemblages demonstrated the UV enhancement on their primary productivity in the presence of PAR, by about 8 % under moderate intensities of solar radiation.     

Spectral Irradiance, Phytoplankton Community Composition and Primary Productivity in a Salt Marsh Estuary, North Inlet, South Carolina, USA

We investigated spatial and temporal changes in spectral irradiance, phytoplankton community composition, and primary productivity in North Inlet Estuary, South Carolina, USA. High concentrations of colored dissolved organic matter (CDOM) were responsible for up to 84 % of the attenuation of photosynthetically available radiation (PAR). Green-yellow wavelengths were the predominant colors of light available at the two sampling sites: Clam Bank Creek and Oyster Landing. Vertical attenuation coefficients of PAR were 0.7–2.1 m^?1 with corresponding euphotic zone depths of 1.5–6.7 m. Phytoplankton biomass (as chlorophyll a [chl a]) varied seasonally with a summer maximum of 16 μg chl a l^?1 and a winter minimum of 1.4 μg chl a l^?1. The phytoplankton community consisted mainly of diatoms, prasinophytes, cryptophytes and haptophytes, with diatoms and prasinophytes accounting for up to 67 % of total chl a. Changes in phytoplankton community composition showed strongest correlations with temperature. Light-saturated chl a-specific rates of photosynthesis and daily primary productivity varied with season and ranged from 1.6 to 14 mg C (mg chl a) ^?1?h^?1 (32–803 mg C m^?3?day^?1). Calculated daily rates added up to an annual carbon fixation rate of 84 g C m^?3?year^?1. Overall, changes in phytoplankton community composition and primary productivity in North Inlet showed a strong dependence on temperature, with PAR and spectral irradiance playing a relatively minor role due to short residence times, strong tidal forcing and vertical mixing.     

Benthic Oxygen Fluxes Measured by Eddy Covariance in Permeable Gulf of Mexico Shallow-Water Sands

Oxygen fluxes across the sediment–water interface reflect primary production and organic matter degradation in coastal sediments and thus provide data that can be used for assessing ecosystem function, carbon cycling and the response to coastal eutrophication. In this study, the aquatic eddy covariance technique was used to measure seafloor–water column oxygen fluxes at shallow coastal sites with highly permeable sandy sediment in the northeastern Gulf of Mexico for which oxygen flux data currently are lacking. Oxygen fluxes at wave-exposed Gulf sites were compared to those at protected Bay sites over a period of 4 years and covering the four seasons. A total of 17 daytime and 14 nighttime deployments, producing 408 flux measurements (14.5 min each), were conducted. Average annual oxygen release and uptake (mean ± standard error) were 191 ± 66 and ?191 ± 45 mmol m^?2 day^?1 for the Gulf sites and 130 ± 57 and ?152 ± 64 mmol m^?2 day^?1 for the Bay sites. Seasonal variation in oxygen flux was observed, with high rates typically occurring during spring and lower rates during summer. The ratio of average oxygen release to uptake at both sites was close to 1 (Bay: 0.9, Gulf: 1.0). Close responses of the flux to changes in light, temperature, bottom current velocity, and wave action (significant wave height) documented tight physical–biological, benthic–pelagic coupling. The increase of the sedimentary oxygen uptake with increasing temperature corresponded to a Q₁₀ temperature coefficient of 1.4 ± 0.3. An increase in flow velocity resulted in increased oxygen uptake (by a factor of 1–6 for a doubling in flow), which is explained by the enhanced transport of organic matter and electron acceptors into the permeable sediment. Benthic photosynthetic production and oxygen release from the sediment was modulated by light intensity at the temporal scale (minutes) of the flux measurements. The fluxes measured in this study contribute to baseline data in a region with rapid coastal development and can be used in large-scale assessments and estimates of carbon transformations.     

Source(s) and cycling of the nonhydrolyzable organic fraction of oceanic particles

A major fraction of particulate organic carbon (POC) in the deep ocean remains molecularly uncharacterized. In an effort to determine the chemical characteristics and source(s) of sinking POC, we studied a nonhydrolyzable fraction of sinking POC using ¹³C NMR (nuclear magnetic resonance) spectroscopy and analytical pyrolysis. ¹³C NMR spectra and products from analytical pyrolysis of the nonhydrolyzable fraction exhibit a strongly aliphatic character that is distinct from that of bulk POC. The aliphatic nature of this fraction is consistent with its low stable carbon isotope values. We hypothesize that the nonhydrolyzable fraction derives to a significant extent from a refractory component of organisms that selectively accumulates, resulting in its manifestation as a major part of POC sinking to the deep ocean and in underlying sediments.     

海洋浮游动物粪便通量

海洋浮游动物粪便颗粒的沉降被认为是碳从海洋表层向海底输送的主要途径之一，对研究碳通量和水层－底栖耦合具有重要意义。综述了有关浮游动物粪便的形态、产生率、分解速度和沉降速度的研究，以及近年来沉积物捕捉器样品的研究。虽然通过粪便产生率和沉降速度估计出的粪便通量很大，但是沉积物中粪便颗粒造成的碳通量所占比例不大。因此，对其它沉积途径的研究不容忽视。     

Transport of particulate organic carbon by the Mississippi River and its fate in the Gulf of Mexico

This study was designed to determine the amount of particulate organic carbon (POC) introduced to the Gulf of Mexico by the Mississippi River and assess the influence of POC inputs on the development of hypoxia and burial of organic carbon on the Louisiana continental shelf. Samples of suspended sediment and supporting hydrographic data were collected from the river and >50 sites on the adjacent shelf. Suspended particles collected in the river averaged 1.8±0.3% organic carbon. Because of this uniformity, POC values (in μmol l^?1) correlated well with concentrations of total suspended matter. Net transport of total organic carbon by the Mississippi-Atchafalaya River system averaged 0.48×10¹² moles y^?1 with 66% of the total organic carbon carried as POC. Concentrations of POC decreased from as high as 600 μmol l^?1 in the river to <0.8 μmol l^?1 in offshore waters. In contrast, the organic carbon fraction of the suspended matter increased from <2% of the total mass in the river to >35% along the shelf at ≥10 km from the river mouth. River flow was a dominant factor in controlling particle and POC distributions; however, time-series data showed that tides and weather fronts can influence particle movement and POC concentrations. Values for apparent oxygen utilization (AOU) increased from ～60 μmol l^?1 to >200 μmol l^?1 along the shelf on approach to the region of chronic hypoxia. Short-term increases in AOU were related to transport of more particle-rich waters. Sediments buried on the shelf contained less organic carbon than incoming river particles. Orgamic carbon and δ¹³C values for shelf sediments indicated 3 that large amounts of both terrigenous and marine organic carbon are being decomposed in shelf waters and sediments to fuel observed hypoxia.     

Ecosystem metabolism and carbon fluxes of a tidally-dominated coastal lagoon

The metabolism and carbon flux in the western sector of the highly dynamic coastal lagoon Ria Formosa (south Portugal) were assessed to elucidate the relative importance of the contribution of the main communities, the treated sewage inputs from the adjacent city of Faro, and the exchange with the adjacent coastal waters to the ecosystem metabolism. The results depict the Ria Formosa as being a highly productive ecosystem dominated by the seagrassZostera noltii. The community dominated by the seagrassCymodocea nodosa had half of the gross production ofZ. noltii, followed by bare sediments and phytoplankton. The net contribution of seagrasses to community metabolism was negligible, as bothZ. noltii andC. nodosa showed a production: respiration ratio close to 1. Benthic microalgae emerge as the most important components of the net metabolism. The western sector of Ria Formosa was in metabolic balance during the summer when the study was done. Even though the total net ecosystem production was 7.22 Kmol C d⁻¹, the error associated with this estimate was 8.38 Kmol C d⁻¹, so ecosystem net production was not significantly different from zero. The Ria Formosa ecosystem is shallow and rapidly flushed by the tides, which force an important exchange of dissolved organic carbon (DOC) and particulate organic carbon (POC) with the adjacent coastal waters. The daily net export rate to the adjacent coastal waters, 0.98 Kmol d⁻¹, represented 7.6% of the net ecosystem production, suggesting that the bulk of the net ecosystem production accumulates within the ecosystem. The organic carbon retention in the western sector of the Ria Formosa is higher than net production, because the allochthonous carbon inputs from urban sewage enter the carbon mass balance with about 40% of the autochthonous processes, at about 1.6 Kmol d⁻¹ of DOC and 2.8 Kmol d⁻¹ of POC. The western sector of Ria Formosa has an organic carbon sink of about 46.4 tons per year. Most of this is harvested in the form of molluscs (clams, cuttlefish, etc.) and fish (sea bream, sea bass, etc.). The total carbon harvested every year in the form of bivalves is about 40 tons, rendering the Ria Formosa the most productive seafood area in Portugal.     

Phytoplankton Biomass and Composition in a River-Dominated Estuary During Two Summers of Contrasting River Discharge

Estuaries located in the northern Gulf of Mexico are expected to experience reduced river discharge due to increasing demand for freshwater and predicted periods of declining precipitation. Changes in freshwater and nutrient input might impact estuarine higher trophic level productivity through changes in phytoplankton quantity and quality. Phytoplankton biomass and composition were examined in Apalachicola Bay, Florida during two summers of contrasting river discharge. The <20 μm autotrophs were the main component (92?±?3 %; n?=?14) of phytoplankton biomass in lower (<25 psu) salinity waters. In these lower salinity waters containing higher dissolved inorganic nutrients, phycocyanin containing cyanobacteria made the greatest contribution to phytoplankton biomass (69?±?3 %; n?=?14) followed by <20 μm eukaryotes (19?±?1 %; n?=?14), and phycoerythrin containing cyanobacteria (4?±?1 %; n?=?14). In waters with salinity from 25 to 35 psu that were located within or in close proximity to the estuary, >20 μm diatoms were an increasingly (20 to 70 %) larger component of phytoplankton biomass. Lower summer river discharges that lead to an areal contraction of lower (5–25 psu) salinity waters composed of higher phytoplankton biomass dominated by small (<20 μm) autotrophs will lead to a concomitant areal expansion of higher (>25 psu) salinity waters composed of relatively lower phytoplankton biomass and a higher percent contribution by >20 μm diatoms. A reduction in summer river discharge that leads to such a change in quantity and quality of estuarine phytoplankton available will result in a reduction in estuarine zooplankton productivity and possibly the productivity of higher trophic levels.     

Submarine Groundwater Discharge as a Source of Dissolved Inorganic Nitrogen and Phosphorus to Coastal Ponds of Southern Rhode Island

Measurements of groundwater-dissolved inorganic nitrogen (nitrate?+?nitrite?+?ammonia) and phosphate concentrations were combined with recent, radium-based, submarine groundwater discharge (SGD) fluxes and prior estimates of SGD determined from Darcy’s Law, a hydrologic model, and total recharge to yield corresponding SGD nutrient fluxes to Ninigret, Point Judith, Quonochontaug, and Winnapaug ponds, located in southern Rhode Island. Results range from 80 to279 mmol N m^?2 year^?1 and 4 to 15 mmol P m^?2 year^?1 for Ninigret, 48 to 265 mmol N m^?2 year^?1 and 4 to 23 mmol P m^?2 year^?1 for Point Judith, 31 to 62 mmol N m^?2 year^?1 and 1 to 2 mmol P m^?2 y^?1 for Quonochontaug, and 668 to 1,586 mmol N m^?2 year^?1 and 29 to 70 mmol P m^?2 year^?1 for Winnapaug ponds, respectively. On a daily basis, the SGD supply of dissolved inorganic nitrogen and phosphorus is estimated to represent ～1–6 % of the total amount of these nutrients in surface waters of Ninigret, Point Judith, and Quonochontaug ponds and up to 84 and 17 % for Winnapaug, respectively, which may reflect a greater SGD nutrient supply to this pond because of the proximity of fertilized golf courses. With regard to the total external input of these essential nutrients, SGD represents 29–45 % of dissolved inorganic nitrogen input to Ninigret, Point Judith, and Quonochontaug ponds and as much as 93 % for Winnapaug pond. For phosphorus, the contribution from SGD represents 59–85 % of the total external input for Ninigret, Point Judith, and Quonochontaug ponds and essentially all of the phosphorus input to Winnapaug pond. Estimated rates of primary productivity potentially supported by the average supply of dissolved inorganic nitrogen from SGD range from 10 g C m^?2 year^?1 for Ninigret, 13 g C m^?2 year^?1 for Point Judith, 4 g C m^?2 year^?1 for Quonochontaug, and as high as 84 g C m^?2 y^?1 for Winnapaug pond. The imputed SGD-derived rates of primary productivity represent 4–9 % of water column primary production for Ninigret, Point Judith, and Quonochontaug ponds, and 74 % for Winnapaug pond, a result that is reasonably comparable to several other coastal environments where estimates of SGD nutrient supply have been reported. The implication is that SGD represents an ecologically significant source of dissolved nutrients to the coastal salt ponds of southern Rhode Island and, by inference, other coastal systems.     

Amino acid composition of suspended particles,sediment-trap material,and benthic sediment in the Potomac Estuary

Sediment trap deployments in estuaries provide a method for estimating the amount of organic material transported to the sediments from the euphotic zone. The amino acid composition of suspended particles, benthic sediment, and sediment-trap material collected at 2.4 m, 5.8 m, and 7.9 m depths in the Potomac Estuary was determined in stratified summer waters, and in well-mixed oxygenated waters (DO) in late fall. The total vertical flow, or flux, of material into the top traps ranged from 3 g m^?2 d^?1 in August to 4.9 g m^?2 d^?1 in October. The carbon and nitrogen fluxes increased in the deepest traps relative to the surface traps during both sampling periods, along with that of the total material flux (up to 47.3 g m^?2 d^?1 in the deepest trap), although the actual weight percent of organic carbon and organic nitrogen decreased with depth. Amino acid concentrations ranged from 129 mg g^?1 in surface water particulate material to 22 mg g^?1 in particulate material in 9-m-deep waters and in the benthic sediment. Amino acid concentrations from 2.4-mg-depth sediment traps averaged 104±29 mg g^?1 in stratified waters and 164±81 mg g^?1 in well-mixed waters. The deep trap samples averaed, 77.3±4.8 mg g^?1 amino acids in summer waters and 37±16 mg g^?1 in oxygenated fall waters. Amino acids comprised 13% to 39% of the organic carbon and 12% to 89% of the orgnaic nitrogen in these samples. Analysis of the flux results suggest that resuspension combined with lateral advection from adjacent slopes can account for up to 27% of the material in the deep traps when the estuary was well-mixed and unstratified. When the estuary was stratified in late summer, the amino acid carbon produced by primary productivity in the euphotic zone decreased by 85% (86% for total organic carbon) at the pycnocline at 6 m depth, leaving up to 15% of the vertical organic flux available for benthic sediment deposition.     

Variations in Concentrations and Fluxes of Dimethylsulfide (DMS) from the Indian Estuaries

In order to examine the variations in concentrations of dimethylsulfide (DMS) and its fluxes to the atmosphere, 25 major and medium estuaries from Indian subcontinent were sampled during wet and dry periods. River discharge brought substantial amount of nutrients and suspended particulate matter (SPM) to the Indian estuaries; however, the concentration of phytoplankton biomass was severely limited by latter due to shallowing of photic depth. Bacillariophyceae was the dominant phytoplankton group in the Indian estuaries followed by green algae, Cyanophyceae, and Dinophyceae. Relatively higher concentrations of DMS were observed in the estuaries located along the east (3.6 ± 5.7 nM) than the west coast of India (0.8 ± 0.3 nM) during wet period whereas no significant differences were observed during dry period. The concentrations of DMS were significantly lower during wet than dry period and it was consistent with the phytoplankton biomass. The slope of the relation between DMS and phytoplankton biomass displayed a significant spatial variation due to contribution of different groups of phytoplankton in the Indian estuaries. The concentrations of DMS in the Indian estuaries were higher than other estuaries in the world except some Chinese estuaries. The annual mean flux (1.95 ± 2.5 μmol m^?2 day^?1) from the Indian estuaries is lower than that of other estuaries in the world, except Pearl River estuary due to inhibition of phytoplankton growth by suspended load and low flushing rates.     

Estimation of Groundwater and Nutrient Fluxes to the Neuse River Estuary, North Carolina

A study was conducted between April 2004 and September 2005 to estimate groundwater and nutrient discharge to the Neuse River estuary in North Carolina. The largest groundwater fluxes were observed to occur generally within 20 m of the shoreline. Groundwater flux estimates based on seepage meter measurements ranged from 2.86?×?10⁸ to 4.33?×?10⁸ m³ annually and are comparable to estimates made using radon, a simple water-budget method, and estimates derived by using Darcy’s Law and previously published general aquifer characteristics of the area. The lower groundwater flux estimate (equal to about 9 m³ s^?1), which assumed the narrowest groundwater discharge zone (20 m) of three zone widths selected for an area west of New Bern, North Carolina, most closely agrees with groundwater flux estimates made using radon (3–9 m³ s^?1) and Darcy’s Law (about 9 m³ s^?1). A groundwater flux of 9 m³ s^?1 is about 40% of the surface-water flow to the Neuse River estuary between Streets Ferry and the mouth of the estuary and about 7% of the surface-water inflow from areas upstream. Estimates of annual nitrogen (333 tonnes) and phosphorus (66 tonnes) fluxes from groundwater to the estuary, based on this analysis, are less than 6% of the nitrogen and phosphorus inputs derived from all sources (excluding oceanic inputs), and approximately 8% of the nitrogen and 17% of the phosphorus annual inputs from surface-water inflow to the Neuse River estuary assuming a mean annual precipitation of 1.27 m. We provide quantitative evidence, derived from three methods, that the contribution of water and nutrients from groundwater discharge to the Neuse River estuary is relatively minor, particularly compared with upstream sources of water and nutrients and with bottom sediment sources of nutrients. Locally high groundwater discharges do occur, however, and could help explain the occurrence of localized phytoplankton blooms, submerged aquatic vegetation, or fish kills.