Scales of nutrient-limited phytoplankton productivity in Chesapeake Bay

The scales on which phytoplankton biomass vary in response to variable nutrient inputs depend on the nutrient status of the plankton community and on the capacity of consumers to respond to increases in phytoplankton productivity. Overenrichment and associated declines in water quality occur when phytoplankton growth rate becomes nutrient-saturated, the production and consumption of phytoplankton biomass become uncoupled in time and space, and phytoplankton biomass becomes high and varies on scales longer than phytoplankton generation times. In Chesapeake Bay, phytoplankton growth rates appear to be limited by dissolved inorganic phosphorus (DIP) during spring when biomass reaches its annual maximum and by dissolved inorganic nitrogen (DIN) during summer when phytoplankton growth rates are highest. However, despite high inputs of DIN and dissolved silicate (DSi) relative to DIP (molar ratios of N∶P and Si∶P>100), seasonal accumulations of phytoplankton biomass within the salt-intruded-reach of the bay appear to be limited by riverine DIN supply while the magnitude of the spring diatom bloom is governed by DSi supply. Seasonal imbalances between biomass production and consumption lead to massive accumulations of phytoplankton biomass (often>1,000 mg Chl-a m^?2) during spring, to spring-summer oxygen depletion (summer bottom water <20% saturation), and to exceptionally high levels of annual phytoplankton production (>400 g m^?2 yr^?1). Nitrogen-dependent seasonal accumulations of phytoplankton biomass and annual production occur as a consequence of differences in the rates and pathways of nitrogen and phosphorus cycling within the bay and underscore the importance of controlling nitrogen inputs to the mesohaline and lower reaches of the bay.     

Non-conservative P and N fluxes and net ecosystem production in San Quintin Bay,México

San Quintin Bay, Mexico, is a hypersaline coastal lagoon where the main external forcing of physical and biogeochemical processes is oceanic. Non-conservative fluxes of inorganic N (ΔDIN) and P (ΔDIP), and aspects of net ecosystem metabolism were studied in this lagoon during August 1995, August 1996, and February 1996, by following the LOICZ budgetary modeling approach. The whole-system water exchange time during summer (≈13 d) was shorter than in winter (≈26 d) as northwesterly winds enhancing mixing with the ocean are more intense during the spring-summer upwelling season. Whole-bay ΔDIP values of +0.2 to +0.3 mmol m^?2 d^?1 in August, and <+0.01 mmol m^?2 d^?1 in February indicate that the system is a net source of dissolved inorganic phosphorus (DIP). DIP fluxes from the Bay to the ocean during August are probably balanced by a net import of particulate organic matter between 1,000–1,300 × 10³ mol C d^?1, equivalent to a net ecosystem production (NEP) between ?24 and ?31 mmol C m^?2 d^?1. ΔDIN showed opposite trends in August 1995 and August 1996, with a net import of 13×10³ mol N d^?1 and a net export of 30× 10³ mol N d^?1, respectively. However, N fixation minus denitrification (“apparent denitrification”) estimates of ≈?4 mmol N m^?2 d^?1 in both periods indicate that San Quintin Bay is a net sink of nitrogen. Results from a 3-box model indicate that during summer Box C, adjacent to the ocean, contributed 70–80% of the excess DIP produced in the whole-system. This observation and high apparent denitrification values of ≈?7 mmol N m^?2 d^?1 at the entrance of the Bay, suggest that the net heterotrophic condition of San Quintin Bay in summer is largely determined by imports of labile phytoplanktonic carbon generated in the adjacent ocean during upwelling.A net flux of organic carbon of 30×10⁶ mol C yr^?1 was estimated from Box C, adjacent to the ocean, to Box B, locally known as Bahia Falsa, which is the area designated for oyster aquaculture in the lagoon. It is estimated that this net organic carbon supply is almost equivalent to the annual oyster food demand; our estimate is that oyster aquaculture in San Quintin Bay accounts for the vast majority of the net heterotrophy of Bahia Falsa.     

Submarine Groundwater Discharge-Derived Nutrient Loads to San Francisco Bay: Implications to Future Ecosystem Changes

Submarine groundwater discharge (SGD) was quantified at select sites in San Francisco Bay (SFB) from radium (²²³Ra and ²²⁴Ra) and radon (²²²Rn) activities measured in groundwater and surface water using simple mass balance box models. Based on these models, discharge rates in South and Central Bays were 0.3?C7.4?m³?day^?1?m^?1. Although SGD fluxes at the two regions (Central and South Bays) of SFB were of the same order of magnitude, the dissolved inorganic nitrogen (DIN) species associated with SGD were different. In the South Bay, ammonium (NH ₄ ⁺ ) concentrations in groundwater were three-fold higher than in open bay waters, and NH ₄ ⁺ was the primary DIN form discharged by SGD. At the Central Bay site, the primary DIN form in groundwater and associated discharge was nitrate (NO ₃ ^? ). The stable isotope signatures (??¹⁵N_NO3 and ??¹⁸O_NO3) of NO ₃ ^? in the South Bay groundwater and surface waters were both consistent with NO ₃ ^? derived from NH ₄ ⁺ that was isotopically enriched in ¹⁵N by NH ₄ ⁺ volatilization. Based on the calculated SGD fluxes and groundwater nutrient concentrations, nutrient fluxes associated with SGD can account for up to 16?% of DIN and 22?% of DIP in South and Central Bays. The form of DIN contributed to surface waters from SGD may impact the ratio of NO ₃ ^? to NH ₄ ⁺ available to phytoplankton with implications to bay productivity, phytoplankton species distribution, and nutrient uptake rates. This assessment of nutrient delivery via groundwater discharge in SFB may provide vital information for future bay ecological wellbeing and sensitivity to future environmental stressors.     

Seasonal growth stimulation of sub-temperate estuarine phytoplankton to nitrogen and phosphorus: An outdoor microcosm experiment

A study of nutrient limitation of phytoplankton biomass production with emphasis on nitrate-nitrogen (NO₃ ^?) and ortho-phosphate-phosphorus (PO₄ ^3?) was conducted in Perdido Bay, Alabama-Florida. The experimental design employed 18-1 outdoor microcosms operated in a static renewal mode. Phytoplankton growth responses (i.e., growth stimulation) measured as chlorophyll a (chl a) fell into three principal categories: primary P stimulation occurred mostly during the cooler months at the upper bay (tidal brackish) and mid bay (lower mesohaline) stations; a total of 12 out of 36 experiments; primary N stimulation occurred mostly during the warmer months primarily at the mid-bay station and infrequently at the upper and lower bay stations (upper mesohaline); a total of 7 out of 36 experiments; and N+P costimulation occurred primarily during the warmer months in the upper bay and mid bay and during both warmer and cooler months of the lower bay; a total of 17 out of 36 experiments. Primary P stimulation was generally associated with high ratios of dissolved inorganic nitrogen (DIN) to dissolved inorganic phosphate (DIP) (ratio range: 18 to 288). Conversely, primary N stimulation was associated with decreasing DIN:DIP ratios (range 8–46). Redfield ratios of particulate organic N (PON) to particulate organic P (POP) often indicated N limitation (i.e., values often less than 10). PON:chl a ratios often indicated N sufficiency, but three occasions were noted where PON:POP and PON:chl a ratios were not congruent. It is difficult to reconcile the inorganic and organic N and P ratios with the relatively low DIP and DIN concentrations. The phytoplankton assemblage appeared not to be strongly nutrient-limited but, given a nutrient increase, responded differentially to N and P, both seasonally and along the longitudinal salinity gradient. Grazing pressure in concert with nutrient limitation was advanced as an hypothesis to explain N+P co-limitation.     

How the Distribution of Anthropogenic Nitrogen Has Changed in Narragansett Bay (RI,USA) Following Major Reductions in Nutrient Loads

Over the past decade, nitrogen (N) loads to Narragansett Bay have decreased by more than 50%. These reductions were, in large part, the direct result of multiple wastewater treatment facility upgrades to tertiary treatment, a process which employs N removal. Here, we document ecosystem response to the N reductions and assess how the distribution of sewage N in Narragansett Bay has changed from before, during, and shortly after the upgrades. While others have observed clear responses when data were considered annually, our seasonal and regional comparisons of pre- and post-tertiary treatment dissolved inorganic nitrogen (DIN) concentrations and Secchi depth data, from bay-wide surveys conducted periodically from the early 1970s through 2016, resulted in only a few subtle differences. Thus, we sought to use stable isotope data to assess how sewage N is incorporated into the ecology of the Bay and how its distribution may have changed after the upgrades. The nitrogen (δ¹⁵N) and carbon (δ¹³C) stable isotope measurements of particulate matter served as a proxy for phytoplankton, while macroalgae served as short-term integrators of water column bio-available N, and hard clams (Mercenaria mercenaria) as integrators of water column production. In contrast to other estuarine stable isotope studies that have observed an increased influence of isotopically lower marine N when sewage N is reduced, the opposite has occurred in Narragansett Bay. The tertiary treatment upgrades have increased the effluent δ¹⁵N values by at least 2‰. The plants and animals throughout Narragansett Bay have similarly increased by 1–2‰, on average. In contrast, the δ¹³C values measured in particulate matter and hard clams have declined by about the same amount. The δ¹⁵N results indicated that, even after the N reductions, sewage N still plays an important role in supporting primary and secondary production throughout the bay. However, the δ¹³C suggests that overall net production in Narragansett Bay has decreased. In the 5 years after the major wastewater treatment facilities came on-line for nutrient removal, oligotrophication has begun but sewage remains the dominant source of N to Narragansett Bay.     

A 2,500-year history of anoxia and eutrophication in Chesapeake Bay

Ongoing monitoring programs and historical data are not sufficient to establish anthropogenic effects on the ecology of Chesapeake Bay. However, stratigraphic records preserved in the sediments can be used to reconstruct both prehistoric and historic sedimentation and water conditions of the bay, including anoxia and eutrophication. Pollen, diatoms, total organic carbon (TOC), nitrogen, total sulfur, and an estimate of the degree of pyritization of iron (DOP) are being used as paleoecological indicators in dated sediment cores for the purpose of reconstructing a long-term environmental history of the bay. Analysis of the data indicates that sedimentation rates, anoxic conditions, and eutrophication have increased in the Chesapeake Bay since the time of European settlement. For example, since initial land clearance around 1760, sedimentation rates have increased from as low as 0.02 cm yr^?1 to an average 0.22 cm yr^?1, and TOC from 0.14 mg cm^?2 yr^?1 to a high 4.96 mg cm^?2 yr^?1. Diatom community structure shows a steady decrease in overall diversity since 1760 and the centric:pennate ratio has increased significantly since 1940.     

Control of nutrient concentrations in the Seekonk-Providence River region of Narragansett Bay,Rhode Island

Six synoptic samplings of nutrient concentrations of the water column and point-source inputs (rivers, sewage treatment plants) were conducted in the Seekonk-Providence River region of Narragansett Bay. Concentrations of nutrients (NH₄ ⁺, NO₂ ^?+NO₃ ^?, PO₄ ^?3, dissolved silicon, particulate N, particulate C) were predicted using a conservative, two-layer box model in order to assess the relative influence of external inputs and internal processes on observed concentrations. Although most nutrients were clearly affected by processes internal to the system, external input and mixing explained most of the variability in and absolute magnitude of observed concentrations, especially for dissolved constituents. In the bay as a whole, two functionally distinct regions can now be identified: the Seekonk-Providence River, where dissolved nutrient concentrations are externally controlled and lower Narragansett Bay where internal processes regulate the behavior of nutrients. A preliminary nitrogen budget suggests that the Seekonk-Providence River exports some 95% of the nitrogen entering the system via point sources and bottom water from upper Narragansett Bay.     

Nitrogen flow and the interaction of Boston harbor with Massachusetts Bay

This paper summarizes evidence that most of the considerable nitrogen loading (～8, 470 mmol total N m^?2 yr^?1) to Boston Harbor (Massachusetts, USA) is expelled to shallow shelf waters of Massachusetts Bay, where it strongly influences ecological dynamics. Examination of nitrogen concentrations in the harbor, compared with loading, indicated that removal processes are active in the harbor. Comparison to other estuarine systems showed that the harbor’s nitrogen concentrations are consistent with its loading, if they are corrected for tidal flushing effects on the water residence time. Furthermore, extensive measurements of sediment denitrification confirmed that rates of N₂ gas loss are high in an absolute sense (～600–800 mmol N m^?2 yr^?1) but nonetheless remove only a small portion (<10%) of the annual land-derived nitrogen loading. Burial in sediments apparently removes only about 2% of the N input, implying export to offshore environments as the major removal process (～88–90% of N input). Western Massachusetts Bay receiving waters were examined for a signature of export from the harbor. Data consistently show a gradient of decreasing nitrogen concentrations from the harbor to about 10–20 km into the bay. In many cases, plots of nitrogen concentrations versus salinity show nearly conservative mixing character, which implies virtual export. Seasonally, the data suggest most of the export from the harbor in winter is as dissolved inorganic forms (NH₄ ⁺, NO₃ ^?, NO₂ ^?). In summer, export is dominated by the outflow of organic nitrogen forms. Chlorophyll export is evident as well, suggesting that the nutritional coupling of the harbor and bay in summer involves organic fertilization of the bay’s surface water. Finally, high-resolution studies over different stages of the tidal cycle help refine understanding of the advection of chlorophyll and stimulation of in situ chlorophyll growth at the seaward edge of the tidal excursion into the bay.     

Effects of menhaden predation of plankton populations in Narragansett Bay, Rhode Island

The Atlantic menhaden,Brevoortia tyrannus, is an abundant plankton-feeding fish that undertakes extensive seasonal migrations, moving from overwintering locations offshore south of Cape Hatteras to the mid-Atlantic Bight and New England inshore waters during spring and summer. A bioenergetic model, based on field and laboratory studies, shows that when large numbers of menhaden enter Narragansett Bay, Rhode Island, during spring and early summer, they significantly influence plankton populations through size-selective grazing and nutrient regeneration. A population biomass of 9.1×10⁶ kg of menhaden feeding for 12 h each day in the upper bay would result, in a substantial reduction of the instantaneous growth rate of the >20-μm phytoplankton. Instantaneous growth rates of zooplankton would be negative if the same population of menhaden was present, resulting in a reduction in the biomass of zooplankton. Given the ambient phytoplankton and zooplankton populations, menhaden could achieve the seasonal growth measured in Narragansett Bay during 1976 by feeding on average about 5 h d^?1. Daily nitrogen excretion rates of the 9.1×10⁶ kg menhaden population were 56.4% of the mean standing stock of ammonia-N in the upper bay. Because menhaden travel in schools their effects are likely to be intense but strongly localized, increasing spatial heterogeneity in the ecosystem. When the fish migrate southward in the fall they transfer between 3.3% and 6.2% of the nitrogen exported annually from the bay.     

Responses of coastal lagoon plant communities to levels of nutrient enrichment: A mesocosm study

An experiment was conducted to quantify the effects of different levels of nutrient enrichment on the plant communities of temperate coastal lagoons, specifically the lagoons of the northeast U.S. Ten mesocosms, each containing coastal water, lagoon sediments, and plants and animals found in natural lagoons, were subjected to five levels of enrichment. Two mesocosms served as controls, and received no experimental nutrient additions. The remaining 8 mesocosms were enriched in duplicate with ammonium plus phosphate at 1.0 and 0.11 mmol N or P m^?2 d^?1, 2.0 and 0.19 mmol N or P m^?2 d^?1, 4.0 and 0.35 mmol N or P m^?2 d^?1, and 8.0 and 0.67 N or P mmol m^?2 d^?1. At all levels of enrichment, and through much of the experiment, water column concentrations of dissolved inorganic nitrogen (DIN) were drawn down to background levels. Despite the efficient drawdown of added DIN even at the highest loadings, differences in plant biomass among the 5 treatments were difficult to detect. Enrichment at the highest loadings increased standing stocks of phytoplankton for one month mid-experiment. No significant effect of loading could be detected for dry biomass of eelgrass (Zostera marina), epiphytic material, drift macroalgae, or for all plant components combined. The experiment has demonstrated that the enrichment responses of coastal lagoons can be diverse, especially at intermediate loadings.     

Denitrification and N2O production in near-shore marine sediments

Methods were developed for determining rates of denitrification in coastal marine sediments by measuring the production of N₂ from undisturbed cores incubated in gas-tight chambers. Denitrification rates at summer temperatures (23°C) in sediment cores from Narragansett Bay, Rhode Island, were about 50μmol N₂m^?2 hr^?1. This nitrogen flux is equal to approximately one-half of the NH⁺₄flux from the sediments at this temperature and is of the magnitude necessary to account for the anomalously low N/P and anomalously high O/N ratios often reported for benthic nutrient fluxes. The loss of fixed nitrogen as N₂ during the benthic remineralization of organic matter, coupled with the importance of benthic remineralization processes in shallow coastal waters may help to explain why the availability of fixed nitrogen is a major factor limiting primary production in these areas. Narragansett Bay sediments are also a source of N₂O, but the amount of nitrogen involved was only about 0.2 μmol m^?2 hr^?1 at 23°C.     

Fluxes of organic carbon in Manukau Harbour, New Zealand

We collated information on the sources and sinks of organic carbon in Manukau Harbour, a shallow temperate estuary. Two contrasting inner harbor regions were considered; the northern region, which is urbanized and receives a major load of sewage wastewater, and the southern region, where allochthonous inputs are dominated by the runoff from small rural streams. Although high levels of dissolved nitrogen in the wastewater supported phytoplankton blooms in the northern region, total primary production there was similar to that in the southern region (ca. 300 g C m^?2yr^?1). By contrast, high concentrations of organic carbon in the wastewater resulted in an additional input to the northern region of 120 g C m^?2 yr^?1. Loads from runoff and streams to both regions were low. At 350 g C m^?2 yr^?1, total respiration in the northern region exceeded total production, so the region was slightly heterotrophic. Respiration was lower in the southern region (270 g C m^?2 yr^?1), which was net autotrophic. Some carbon was exported from each region to the outer harbour (50–80 g C m^?2 yr^?1). Dissolved oxygen levels in the northern region were somewhat depleted at times; and the high numbers of microzooplankton indicated consumption was enhanced there. Apart from a relatively small area of organic enrichment close to the wastewater discharge, benthic consumers in the harbor appeared to be limited by physical disturbance (by wind-waves) rather than by food availability. Improved wastewater treatment is expected to substantially reduce the allochthonous input to the northern region, with the total input of carbon in the future being only slightly higher than that to the southern region.     

Going West: Nutrient Limitation of Primary Production in the Northern Gulf of Mexico and the Importance of the Atchafalaya River

To investigate controls on phytoplankton production along the Louisiana coastal shelf, we mapped salinity, nutrient concentrations (dissolved inorganic nitrogen (DIN) and phosphorus (P_i), silicate (Si)), nutrient ratios (DIN/P_i), alkaline phosphatase activity, chlorophyll and ¹⁴C primary productivity on fine spatial scales during cruises in March, May, and July 2004. Additionally, resource limitation assays were undertaken in a range of salinity and nutrient regimes reflecting gradients typical of this region. Of these, seven showed P_i limitation, five revealed nitrogen (N) limitation, three exhibited light (L) limitation, and one bioassay had no growth. We found the phytoplankton community to shift from being predominately N limited in the early spring (March) to P limited in late spring and summer (May and July). Light limitation of phytoplankton production was recorded in several bioassays in July in water samples collected after peak annual flows from both the Mississippi and Atchafalaya Rivers. We also found that organic phosphorus, as glucose-6-phosphate, alleviated P limitation while phosphono-acetic acid had no effect. Whereas DIN/P_i and DIN/Si ratios in the initial water samples were good predictors of the outcome of phytoplankton production in response to inorganic nutrients, alkaline phosphatase activity was the best predictor when examining organic forms of phosphorus. We measured the rates of integrated primary production (0.33?C7.01 g C m^?2 d^?1), finding the highest rates within the Mississippi River delta and across Atchafalaya Bay at intermediate salinities. The lowest rates were measured along the outer shelf at the highest salinities and lowest nutrient concentrations (<0.1 ??M DIN and Pi). The results of this study indicate that P_i limitation of phytoplankton delays the assimilation of riverine DIN in the summer as the plume spreads across the shelf, pushing primary production over a larger region. Findings from water samples, taken adjacent the Atchafalaya River discharge, highlighted the importance of this riverine system to the overall production along the Louisiana coast.     

Annual phytoplankton metabolism in Narragansett Bay calculated from survey field measurements and microcosm observations

Field surveys of phytoplankton metabolism, based on oxygen changes, were made in Narragansett Bay from 1971–73. Annual daytime net production varied from 218 g C per m² per yr in the East Passage to 429 g C per m² per yr in the Providence River. The area based average for the bay was 269 g C per m² per yr. The area based average night respiration was 159 g C per m² per yr resulting in an annual net carbon available for export or to the benthos of 110 g C per m² per yr. A set of microcosms, operated so as to simulate the Bay, had an annual net production of 276 g C per m² per yr and a night respiration of 163 g C per m² per yr resulting in an annual net carbon available for export or to the benthos of 113 g C per m² per yr. *** DIRECT SUPPORT *** A01BY015 00002     

Silver in San Francisco Bay estuarine waters

Spatial gradients of silver concentrations in the surface waters of San Francisco Bay reveal substantial anthropogenic perturbations of the biogeochemical cycle of the element throughout the estuarine system. The most pronounced perturbations are in the south bay, where dissolved (<0.45 μm) silver concentrations are as high as 250 pM. This is more than one order-of-magnitude above baseline concentrations in the northern reach of the estuary (6 pM) and approximately two orders-of-magnitude above natural concentrations in adjacent coastal waters (3 pM). The excess silver is primarily attributed to wastewater discharges of industrial silver to the estuary on the order of 20 kg d^?1. The contamination is most evident in the south bay, where wastewater discharges of silver are on the order of 10 kg d^?1 and natural freshwater discharges are relatively insignificant. The limited amount of freshwater flushing in the south bay was exacerbated by persistent drought conditions during the study period. This extended the hydraulic residence time in the south bay (≥160 d), and revealed the apparent seasonal benthic fluxes of silver from anthropogenically contaminated sediments. These were conservatively estimated to average ≈16 nmol m^?2 d^?1 in the south bay, which is sufficient to replace all of the dissolved silver in the south bay within 22 d. Benthic fluxes of silver throughout the estuary were estimated to average ≈11 nmol m^?2 d^?1, with an annual input of approximately 540 kg yr^?1 of silver to the system. This dwarfs the annual fluvial input of silver during the study period (12 kg yr^?1) and is equivalent to approximately 10% of the annual anthropogenic input of silver to the estuary (3,700–7,200 kg yr^?1). It is further speculated that benthic fluxes of silver may be greater than or equal to waste water fluxes of silver during periods of intense diagenic remobilization. However, all inputs of dissolved silver to the estuary are efficiently sorbed by suspended particulates, as evidenced by the relatively constant conditional distribution coefficient for silver throughout the estuary (K_d≈10⁵).     

Coupling Between the Coastal Ocean and Yaquina Bay,Oregon: Importance of Oceanic Inputs Relative to Other Nitrogen Sources

Understanding of the role of oceanic input in nutrient loadings is important for understanding nutrient and phytoplankton dynamics in estuaries adjacent to coastal upwelling regions as well as determining the natural background conditions. We examined the nitrogen sources to Yaquina Estuary (Oregon, USA) as well as the relationships between physical forcing and gross oceanic input of nutrients and phytoplankton. The ocean is the dominant source of dissolved inorganic nitrogen (DIN) and phosphate to the lower portion of Yaquina Bay during the dry season (May through October). During this time interval, high levels of dissolved inorganic nitrogen (primarily in the form of nitrate) and phosphate entering the estuary lag upwelling favorable winds by 2 days. The nitrate and phosphate levels entering the bay associated with coastal upwelling are correlated with the wind stress integrated over times scales of 4–6 days. In addition, there is a significant import of chlorophyll a to the bay from the coastal ocean region, particularly during July and August. Variations in flood-tide chlorophyll a lag upwelling favorable winds by 6 days, suggesting that it takes this amount of time for phytoplankton to utilize the recently upwelled nitrogen and be transported across the shelf into the estuary. Variations in water properties determined by ocean conditions propagate approximately 11–13 km into the estuary. Comparison of nitrogen sources to Yaquina Bay shows that the ocean is the dominant source during the dry season (May to October) and the river is the dominant source during the wet season with watershed nitrogen inputs primarily associated with nitrogen fixation on forest lands.     

Estimating secondary production and benthic consumption in monitoring studies: A case study of the impacts of dredged material disposal in Galveston Bay, Texas

We examined the effects of dredged material disposal on benthic macroinvertebrates in Galveston Bay, Texas, USA, while investigating the utility of estimating secondary production with estimation methods that have less rigorous data requirements than most classical techniques. Production estimates were compared to estimates of benthic consumption by blue crabs, shrimp, and epibenthic fish. There was no evidence that dredged material disposal had a detrimental impact on benthic production; however, production was low throughout the entire bay the year following dredged material disposal, which may have obscured an assessment of the impact of disposal. In fact, disposal sites yielded both the highest production estimates and species richness in both the upper and lower bay areas 2 yr after disposal. Of the five estimation methods used, two that incorporated environmental parameters (temperature and depth) yielded similar and moderate results, ranging from 1.1 g ash-free dry weight m² yr¹ to 26.9 g ash-free dry weight (AFDW) m^?2 yr^?1 over the 4 yr studied. Daily food ration estimates applied to fishery-independent trawl-survey data yielded overall benthic consumption estimates ranging from 1.1 g AFDW m^?2 to 1.7 g AFDW m^?2. A second method of estimating consumption, which used transfer efficiency estimates and annual fisheries statistics produced slightly lower benthic consumption estimates (0.72–1.13 g AFDW m^?2). The average consumption estimate exceeded benthic production in the upper bay in one of the 4 yr for which benthic production was estimated. In years with high benthic production, the estimated benthic food requirement of epibenthic predators was roughly 10–15% of benthic production. Variation in annual benthic production estimates was two to three times greater than the variation in consumption estimates.     

Dynamics of NH4 + and NO3 − uptake in the water column of the Neuse River Estuary,North Carolina

In an attempt to more fully understand the dissolved inorganic nitrogen dynamics of the Neuse River estuary, ¹⁵NH₄ ⁺ and ¹⁵NO₃ ^? uptake rates were measured and daily depth-integrated rates calculated for seven stations distributed along the salinity gradient. Measurements were made at 2–3-wk intervals from March 1985 to February 1989. Significant dark NH₄ ⁺ uptake occurred and varied both spatially and seasonally, accounting for as much as 95% of light uptake with the median being 33%. Apparent NH₄ ⁺ uptake ranged from 0.001 μmol N 1^?1 h^?1 to 4.2 μmol N 1^?1 h^?1, with highest rates occurring during late summer-fall in the oligohaline estuary. Apparent NH₄ ⁺ uptake was significantly related to NH₄ ⁺ concentration (p<0.01); however, the regression explained <3% of the variation. Daily-integrated NH₄ ⁺ uptake ranged from 0.1 mmol N m^?2 d^?1 to 133 mmol N m^?2 d^?1 and followed the trend of apparent uptake. Annual NH₄ ⁺ uptake of the estuary was significantly lower in 1988 than for any other year. Dark uptake of NO₃ ^? was only 14% of maximum light uptake. Apparent NO₃ ^? uptake rates ranged from 0.001 μmol N 1^?1 h^?1 to 1.84 μmol N 1^?1 h^?1 with highest rates occurring in the oligohaline estuary. Apparent NO₃ ^? uptake was significantly related to NO₃ ^? concentration (p<0.01); however, the regression explained <5% of the variation. In general, NO₃ ^? uptake was only 20% of total dissolved inorganic nitrogen (DIN) uptake. Daily-integrated NO₃ ^? uptake ranged from 0.1 mmol N m^?2 d^?1 to 53 mmol N m^?2 d^?1 and followed similar patterns of apparent uptake. Annual NH₄ ⁺ uptake was 11.39 mol N m^?2 yr^?1, 10.28 mol N m^?2 Yr^?1, 10.93 mol N m^?2 yr^?1, and 7.38 mol N m^?2 yr^?1, and 1.84 mol N m^?2 yr^?1, with the 4-yr mean being 10.0. Annual NO₃ ^? uptake was 3.12 mol N m^?2 yr^?1, 3.40 mol N m^?2 yr^?1, 1.96 mol N m^?2 yr^?1, and 1.84 mol N m^?2 yr^?1, with the 4-yr mean being 2.6. The total annual DIN uptake was more than twice published estimates of phytoplankton DIN demand, indicating that there is an important heterotrophic component of DIN uptake occurring in the water column. The extrapolation of nitrogen demand from primary productivity results in serious underestimates of estuarine nitrogen demand for the Neuse River estuary and may be true for other estuaries as well.     

Rates of nitrification along an estuarine gradient in Narragansett Bay

Rates of pelagic nitrification, measured using N-Serve-sensitive [¹⁴C]bicarbonate uptake, varied by as much as an order-of-magnitude among three sites along the salinity gradient of Narragansett Bay (Rhode Island, United States). Rates were always higher at the Providence River estuary site (0.04–11.2 μmol N I^?1 d^?1) than at either the lower Narragansett Bay site (0.02–0.98 μmol N I^?1d^?1) or the freshwater Blackstone River site (0.04–1.7 μmol N I^?1d^?1). Although temperature was the most important variable regulating the annual cycle of nitrification, ammonium concentrations were most likely responsible for the large differences in rates among the three sites in summer. At the levels found in this estuarine system, salinity and concentrations of oxygen or total suspended matter did not appear to have a direct measurable effect on nitrification and pH did only occasionally. Nitrification played an important role in the nitrogen cycle at all three sites. In Narragansett Bay, nitrification contributed 55% of the NO₂ ^? and NO₃ ^? entering annually, and was the major source during spring and summer. Water from offshore was the only other large source of NO₂ ^? and NO₃ ^?, contributing 34%. High summer rates of nitrification could support much of the phytoplankton uptake of NO₂ ^? and NO₃ ^?. In the Providence River estuary, the largest annual input of NO₂ ^? and NO₃ ^? was from rivers (54%), although nitrification (28%) and water from lower portions of the bay (11%) also made large contributions. Again, nitrification was most important in the summer. The high rates of nitrification in the Providence River estuary during summer were also likely to be important in terms of oxygen demand, and the production of nitric and nitrous oxides. In the Blackstone River, NO₂ ^? and NO₃ ^? concentrations increased as the river flowed through Rhode Island, and nitrification was a possible source.     

Nutrient dynamics in the Pomeranian Bay (southern Baltic): Impact of the Oder River outflow

The Pomeranian Bay is a coastal region fed by the Oder River, one of the seven largest Baltic rivers, whose waters flow through a large and complex estuarine system before entering the bay. Nutrients (NO₃ ⁻, NO₂ ⁻, NH₄ ⁺, Ntot, PO₄ ³⁻, P_tot, DSi), chlorophylla concentrations, oxygen content, salinity, and temperature were measured in the Pomeranian Bay in nine seasonally distributed cruises during 1993–1997. Strong spatial and temporal patterns were observed and they were governed by: the seasonally variable riverine water-nutrient discharges, the seasonally variable uptake of nutrients and their cycling in the river estuary and the Bay, the character of water exchange between the Pomeranian Bay and the Szczecin Lagoon, and the water flow patterns in the Bay that are dominated by wind-driven circulation. Easterly winds resulted in water and nutrient transport along the German coastline, while westerly winds confined the nutrient rich riverine waters to the Polish coast and transported them eastward beyond the study area. Two water masses, coastal and open, characterized by different chemical and physical parameters and chla content were found in the Bay independently of the season. The role of the Oder estuary in nutrient transformation, as well as the role of temperature in transformation processes is stressed in the paper. The DIN:DIP:DSi ratio indicated that phosphorus most probably played a limiting role in phytoplankton production in the Bay in spring, while nitrogen did the same in summer. During the spring bloom, predominated by diatoms, the DSi:DIN ratio dropped to 0.1 in the coastal waters and to 0.6 in the open bay waters, pointing to silicon limitation of diatom growth, similar to what is being observed in other Baltic regions.