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Biogeochemistry | 1996

The fate of nitrogen and phosphorus at the land-sea margin of the North Atlantic Ocean

Scott W. Nixon; J. W. Ammerman; Larry P. Atkinson; V. M. Berounsky; Gilles Billen; William C. Boicourt; Walter R. Boynton; Thomas M. Church; D. M. Ditoro; Ragnar Elmgren; J. H. Garber; Anne E. Giblin; R. A. Jahnke; N.J.P. Owens; M. E. Q. Pilson; Sybil P. Seitzinger

Five large rivers that discharge on the western North Atlantic continental shelf carry about 45% of the nitrogen (N) and 70% of the phosphorus (P) that others estimate to be the total flux of these elements from the entire North Atlantic watershed, including North, Central and South America, Europe, and Northwest Africa. We estimate that 61 · 109 moles y−1 of N and 20 · 109 moles y−1 of P from the large rivers are buried with sediments in their deltas, and that an equal amount of N and P from the large rivers is lost to the shelf through burial of river sediments that are deposited directly on the continental slope. The effective transport of active N and P from land to the shelf through the very large rivers is thus reduced to 292 · 109 moles y−1 of N and 13 · 109 moles y−1 of P.The remaining riverine fluxes from land must pass through estuaries. An analysis of annual total N and total P budgets for various estuaries around the North Atlantic revealed that the net fractional transport of these nutrients through estuaries to the continental shelf is inversely correlated with the log mean residence time of water in the system. This is consistent with numerous observations of nutrient retention and loss in temperate lakes. Denitrification is the major process responsible for removing N in most estuaries, and the fraction of total N input that is denitrified appears to be directly proportional to the log mean water residence time. In general, we estimate that estuarine processes retain and remove 30–65% of the total N and 10–55% of the total P that would otherwise pass into the coastal ocean. The resulting transport through estuaries to the shelf amounts to 172–335 · 109 moles y−1 of N and 11–19 · 109 moles y−1 of P. These values are similar to the effective contribution from the large rivers that discharge directly on the shelf.For the North Atlantic shelf as a whole, N fluxes from major rivers and estuaries exceed atmospheric deposition by a factor of 3.5–4.7, but this varies widely among regions of the shelf. For example, on the U.S. Atlantic shelf and on the northwest European shelf, atmospheric deposition of N may exceed estuarine exports. Denitrification in shelf sediments exceeds the combined N input from land and atmosphere by a factor of 1.4–2.2. This deficit must be met by a flux of N from the deeper ocean. Burial of organic matter fixed on the shelf removes only a small fraction of the total N and P input (2–12% of N from land and atmosphere; 1–17% of P), but it may be a significant loss for P in the North Sea and some other regions. The removal of N and P in fisheries landings is very small. The gross exchange of N and P between the shelf and the open ocean is much larger than inputs from land and, for the North Atlantic shelf as a whole, it may be much larger than the N and P removed through denitrification, burial, and fisheries. Overall, the North Atlantic continental shelf appears to remove some 700–950· 109 moles of N each year from the deep ocean and to transport somewhere between 18 and 30 · 109 moles of P to the open sea. If the N and P associated with riverine sediments deposited on the continental slope are included in the total balance, the net flux of N to the shelf is reduced by 60 · 109 moles y−1 and the P flux to the ocean is increased by 20 · 109 moles y−1. These conclusions are quite tentative, however, because of large uncertainties in our estimates of some important terms in the shelf mass balance.


Science | 1984

Chesapeake Bay Anoxia: Origin, Development, and Significance

Charles B. Officer; Robert B. Biggs; Jay L. Taft; L. Eugene Cronin; Mary A. Tyler; Walter R. Boynton

Anoxia occurs annually in deeper waters of the central portion of the Chesapeake Bay and presently extends from Baltimore to the mouth of the Potomac estuary. This condition, which encompasses some 5 billion cubic meters of water and lasts from May to September, is the result of increased stratification of the water column in early spring, with consequent curtailment of reoxygenation of the bottom waters across the halocline, and benthic decay of organic detritus accumulated from plankton blooms of the previous summer and fall. The Chesapeake Bay anoxia appears to have had significant ecological effects on many marine species, including several of economic importance.


Estuaries | 1995

Inputs, transformations, and transport of nitrogen and phosphorus in Chesapeake Bay and selected tributaries

Walter R. Boynton; J. H. Garber; Robert M. Summers; W. M. Kemp

In this paper we assemble and analyze quantitative annual input-export budgets for total nitrogen (TN) and total phosphorus (TP) for Chesapeake Bay and three of its tributary estuaries (Potomac, Patuxent, and Choptank rivers). The budgets include estimates of TN and TP sources (point, diffuse, and atmospheric), internal losses (burial in sediments, fisheries yields, and denitrification), storages in the water column and sediments, internal cycling rates (zooplankton excretion and net sediment-water flux), and net downstream exchange. Annual terrestrial and atmospheric inputs (average of 1985 and 1986 data) of TN and TP ranged from 4.3 g TN m−2 yr−1 to 29.3 g TN m−2 yr−1 and 0.32 g TP m−2 yr−1 to 2.42 g TP m−2 yr−1, respectively. These rates of TN and TP input represent 6-fold to 8-fold and 13-fold to 24-fold increases in loads to these systems since the precolonial period. A recent 11-yr record for the Susquehanna River indicates that annual loads of TN and TP have varied by about 2-fold and 4-fold, respectively. TN inputs increased and TP inputs decreased during the 11-yr period. The relative importance of nutrient sources varied among these estuaries: point sources of nutrients delivered about half the annual TN and TP load to the Patuxent and nearly 60% of TP inputs to the Choptank; diffuse sources contributed 60–70% of the TN and TP inputs to the mainstream Chesapeake and Potomac River. The direct deposition of atmospheric wet-fall to the surface waters of these estuaries represented 12% or less of annual TN and TP loads except in the Choptank River (37% of TN and 20% of TP). We found direct, although damped, relationships between annual rates of nutrient input, water-column and sediment nutrient stocks, and nutrient losses via burial in sediments and denitrification. Our budgets indicate that the annual mass balance of TN and TP is maintained by a net landward exchange of TP and, with one exception (Choptank River), a net seaward transport of TN. The budgets for all systems revealed that inorganic nutrients entering these estuaries from terrestrial and atmospheric sources are rapidly converted to particulate and organic forms. Discrepancies between our budgets and others in the literature were resolved by the inclusion of sediments derived from shoreline erosion. The greatest potential for errors in our budgets can be attributed to the absence of or uncertainties in estimates of atmospheric dry-fall, contributions of nutrients via groundwater, and the sedimentation rates used to calculate nutrient burial rates.


Estuaries | 2004

Hypoxia in Chesapeake Bay, 1950-2001 : Long-term change in relation to nutrient loading and river flow

James D. Hagy; Walter R. Boynton; Carolyn W. Keefe; Kathryn V. Wood

A 52-yr record of dissolved oxygen in Chesapeake Bay (1950–2001) and a record of nitrate (NO3−) loading by the Susquehanna River spanning a longer period (1903, 1945–2001) were assembled to describe the long-term pattern of hypoxia and anoxia in Chesapeake Bay and its relationship to NO3− loading. The effect of freshwater inflow on NO3− loading and hypoxia was also examined to characterize its effect at internannual and longer time scales. Year to year variability in river flow accounted for some of the observed changes in hypoxic volume, but the long-term increase was not due to increased river flow. From 1950–2001, the volume of hypoxic water in mid summer increased substantially and at an accelerating rate. Predicted anoxic volume (DO<0.2 mg I−1) at average river flow increased from zero in 1950 to 3.6×109 m3 in 2001. Severe hypoxia (DO<1.0 mg I−1) increased from 1.6×109 to 6.5×109 m3 over the same period, while mild hypoxia (DO<2.0 mg I−1) increased from 3.4×109 to 9.2×109 m3. NO3− concentrations in the Susquehanna River at Harrisburg, Pennsylvania, increased up to 3-fold from 1945 to a 1989 maximum and declined through 2001. On a decadal average basis, the superposition of changes in river flow on the long-term increase in NO3− resulted in a 2-fold increase in NO3− loading from the Susquehanna River during the 1960s to 1970s. Decadal average loads were subsequently stable through the 1990s. Hypoxia was positively correlated with NO3− loading, but more extensive hypoxia was observed in recent years than would be expected from the observed relationship. The results suggested that the Bay may have become more susceptible to NO3− loading. To eliminate or greatly reduce anoxia will require reducing average annual total nitrogen loading to the Maryland mainstem Bay to 50×106 kg yr−1, a reduction of 40% from recent levels.


Estuarine Comparisons#R##N#Proceedings of the Sixth Biennial International Estuarine Research Conference, Gleneden Beach, Oregon, November 1–6, 1981 | 1982

A comparative analysis of nutrients and other factors influencing estuarine phytoplankton production.

Walter R. Boynton; W M Kemp; C W Keefe

Abstract We reviewed data concerning phytoplankton production, chlorophyll a, and associated physical and chemical variables from 63 different estuarine systems. Data were analyzed statistically to test hypotheses regarding algal productivity and factors regulating temporal patterns. Prior to statistical analysis, estuarine systems were classified into four groups based on criteria of physical circulation and geomorphology. Analysis of grouped data indicated that algal production and biomass were consistently high in warm periods of the year in a broad spectrum of estuaries and that ratios of available nitrogen to phosphorus were low during periods of high production, except in highly eutrophic systems. In general, phytoplankton production and biomass exhibited weak correlations with a variety of physical and chemical state variables, perhaps indicating the significance of rate processes as opposed to standing stocks in regulating these important features of estuarine systems. A six-year time series of measurements of algal production and chlorophyll a at stations in middle Chesapeake Bay exhibited considerable year-to-year variability, with a three-fold range in peak values. Summertime maxima were strongly related to annual loadings of both nitrogen (N) and phosphorus (P) but annual production appeared to be sustained primarily on recycled nitrogen and phosphorus. To generalize from these findings, N and P loading rates were estimated for 14 different estuarine systems, and a significant positive relationship was obtained between phytoplankton production and nitrogen (but not phosphorus) inputs.


Marine Geology | 1984

The influence of waves and seagrass communities on suspended particulates in an estuarine embayment

Larry G. Ward; W. Michael Kemp; Walter R. Boynton

Resuspension of bottom sediments by waves, corresponding changes in suspended particulate material (SPM) concentrations in the overlying water column, and transport pathways of SPM were investigated in a shallow estuarine embayment colonized by seagrass communities in Chesapeake Bay. In shallow (<2 m), unvegetated regions significant resuspension of bottom sediments was evident when northerly winds exceeded 25 km h−1, increasing SPM concentrations up to 10-fold. High concentrations of SPM generated by resuspension dissipated rapidly (within 24 h) after winds became calm. Patterns of SPM along the embayments depth gradient suggest that part of this resuspended material was transported offshore into deeper reaches of the estuary. In areas of the embayment colonized by seagrasses, wave energy was attenuated by the vegetation, suppressing resuspension and enhancing deposition. As a result, SPM concentrations were significantly lower inside seagrass beds than in adjacent unvegetated areas. During periods of high winds when wave induced resuspension occurred in unvegetated areas, SPM concentrations remained unchanged inside the bed at normal water levels. However, when water levels were elevated by spring tides or storm surges, plants were less effective at attenuating wave energy, and SPM concentrations increased inside the seagrass bed due to resuspension and advective processes. Calculations based on the results of this study indicate that sedimentation rates are substantially higher in seagrass communities than in unvegetated areas.


Estuaries | 1996

Sediment-water oxygen and nutrient exchanges along the longitudinal axis of Chesapeake Bay: Seasonal patterns, controlling factors and ecological significance

Jean L. W. Cowan; Walter R. Boynton

Sediment-water oxygen and nutrient (NH4+, NO3−+NO2−, DON, PO43−, and DSi) fluxes were measured in three distinct regions of Chesapeake Bay at monthly intervals during 1 yr and for portions of several additional years. Examination of these data revealed strong spatial and temporal patterns. Most fluxes were greatest in the central bay (station MB), moderate in the high salinity lower bay (station SB) and reduced in the oligohaline upper bay (station NB). Sediment oxygen consumption (SOC) rates generally increased with increasing temperature until bottom water concentrations of dissolved oxygen (DO) fell below 2.5 mg l−1, apparently limiting SOC rates. Fluxes of NH4+ were elevated at temperatures >15°C and, when coupled with low bottom water DO concentrations (<5 mg l−1), very large releases (>500 μmol N m−2 h−1) were observed. Nitrate + nitrite (NO3−+NO2−) exchanges were directed into sediments in areas where bottom water NO3−+NO2− concentrations were high (>18 μM N); sediment efflux of NO3−+NO2− occurred only in areas where bottom water NO3−+NO2− concentrations were relatively low (<11 μM N) and bottom waters well oxygenated. Phosphate fluxes were small except in areas of hypoxic and anoxic bottom waters; in those cases releases were high (50–150 μmol P m−2 h−1) but of short duration (2 mo). Dissolved silicate (DSi) fluxes were directed out of the sediments at all stations and appeared to be proportional to primary production in overlying waters. Dissolved organic nitrogen (DON) was released from the sediments at stations NB and SB and taken up by the sediments at station MB in summer months; DON fluxes were either small or noninterpretable during cooler months of the year. It appears that the amount and quality of organic matter reaching the sediments is of primary importance in determining the spatial variability and interannual differences in sediment nutrient fluxes along the axis of the bay. Surficial sediment chlorophyll-a, used as an indicator of labile sediment organic matter, was highly correlated with NH4−, PO43−, and DSi fluxes but only after a temporal lag of about 1 mo was added between deposition events and sediment nutrient releases. Sediment O:N flux ratios indicated that substantial sediment nitrification-denitrification probably occurred at all sites during winter-spring but not summer-fall; N:P flux ratios were high in spring but much less than expected during summer, particularly at hypoxic and anoxic sites. Finally, a comparison of seasonal N and P demand by phytoplankton with sediment nutrient releases indicated that the sediments provide a substantial fraction of nutrients required by phytoplankton in summer, but not winter, especially in the mid bay region.


Ecological Economics | 1995

Ecological economic modeling and valuation of ecosystems

Nancy E. Bockstael; Robert Costanza; I. Strand; Walter R. Boynton; K. Bell; Lisa Wainger

Abstract We are attempting to integrate ecological and economic modeling and analysis in order to improve our understanding of regional systems, assess potential future impacts of various land-use, development, and agricultural policy options, and to better assess the value of ecological systems. Starting with an existing spatially articulated ecosystem model of the Patuxent River drainage basin in Maryland, we are adding modules to endogenize the agricultural components of the system (especially the impacts of agricultural practices and crop choice) and the process of land-use decision making. The integrated model will allow us to evaluate the indirect effects over long time horizons of current policy options. These effects are almost always ignored in partial analyses, although they may be very significant and may reverse many long-held assumptions and policy predictions. This paper is a progress report on this modeling effort, indicating our motivations, ideas, and plans for completion.


Estuaries | 1996

A comparative analysis of eutrophication patterns in a temperate coastal lagoon

Walter R. Boynton; L. Murray; J. D. Hagy; C. Stokes; W. M. Kemp

The coastal bays and lagoons of Maryland extend the full length of the states Atlantic coast and compose a substantial ecosystem at the land-sea margin that is characterized by shallow depth, a well-mixed water column, slow exchange with the coastal ocean, and minimal freshwater input from the land. For at least 25 years, various types of measurements have been made intermittently in these systems, but almost no effort has been made to determine if water quality or habitat conditions have changed over the years or if distinctive spatial gradients in these features have developed in response to changing land uses. The purpose of this work was to examine this fragmented database and determine if such patterns have emerged and how they may be related to land uses. Turbidity, dissolved inorganic phosphate, algal biomass, and primary production rates in most areas of the coastal bays followed a regular seasonal pattern, which was well correlated with water temperature. Nitrate concentrations were low (<5 μM), and only modestly higher in tributary creeks (<20 μM). Additionally, there was little indication of the spring bloom typical of river-dominated systems. There does appear to be a strong spatial gradient in water quality conditions (more eutrophic in the upper bays, especially in tributary creeks). Comparisons of water quality data collected between 1970 and 1991 indicate little temporal change in most areas and some small improvements in a few areas, probably related to decreases in point-source discharges. Seagrass communities were once extensive in these systems but at present are restricted to the eastern portion of the lower bays where water clarity is sufficient to support plant survival. Even in these areas, seagrass densities have recently decreased. Examination of diel dissolved oxygen data collected in the summer indicates progressively larger diel excursions from lower to upper bays and from open bays to tributary subsystems; however, hypoxic conditions (<2 mg 1−1) were rarely observed in any location. Nitrogen input data (point, surface runoff, groundwater and atmospheric deposition to surface waters) were assembled for seven regions of the coastal bay system; annual loading rates ranged from 2.4 g N m−2 yr−1 to 39.7 g N m−2 yr−1. Compared with a sampling of loading rates to other coastal systems, those to the upper and lower bays were low while those to tributaries were moderate to high. Regression analysis indicated significant relationships between annual nitrogen loading rates and average annual total nitrogen and chlorophyll a concentrations in the water column. Similar analyses also indicated significant relationships between chlorophyll a and the magnitude of diel dissolved oxygen changes in the water column. It is concluded that these simple models, which could be improved with a well-designed monitoring program, could be used as quantitative management tools to relate habitat conditions to nutrient loading rates.


Kennedy, V S (Ed ) Estuarine Perspectives; 5th Biennial International Estuarine Research Conference, Jekyll Island, Ga , Usa, Oct 7-12, 1979 Xxi+533p Academic Press, Inc | 1980

Nutrient fluxes across the sediment water interface in the turbid zone of a coastal plain estuary

Walter R. Boynton; W. Michael Kemp; Carl G. Osborne

Abstract Oxygen and nutrient fluxes across the sediment-water interface were measured over an annual cycle in the turbid portion of the Patuxent Estuary. Benthic respiration rates ranged from 0.5 to 4.1 g O 2 m –2 d –1 and were positively correlated with temperature and primary production. Net fluxes of ammonium (NH 4 + ) and dissolved inorganic phosphorus (DIP) ranged from –105 to 1584 μg-at N m –2 h –1 and 1 to 295 μg-at P m –2 h –1 respectively. These rates, which were positively correlated with temperature, are among the highest yet reported in the literature. Fluxes of nitrate plus nitrite were small during summer when water column concentrations were low, but high and directed into the sediments during winter when water column concentrations were high. In general it appears that nutrient fluxes across the sediment-water interface represent an important source to the water column in summer when photosynthetic demand is high and water column stocks are low and, conversely, serve as a sink in winter when demand is low and water column stocks high, thereby serving a “buffering” function between supply and demand. A simple budget of sediment-water exchanges and storages of nitrogen indicated that, of the total particulate nitrogen deposited annually onto the sediments, about 34% was returned to the water column as NH 4 + , 41% was stored as particulate nitrogen in the sediments and, by difference, we estimated that the remaining 24% was denitrified. We also observed considerable uptake of nitrate by the sediments during winter months (1.1 g-at m –2 y –1 ), suggesting an additional source of annual denitrification, since this nitrate uptake was not accompanied by ammonium release back to the water column. The ecological implications of these large nutrient fluxes are discussed in terms of sources and sinks of nutrients, as well as couplings with carbon productivity.

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W. Michael Kemp

University of Maryland Center for Environmental Science

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James G. Sanders

Skidaway Institute of Oceanography

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Jeremy M. Testa

Chesapeake Biological Laboratory

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James D. Hagy

University of Maryland Center for Environmental Science

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Christopher F. D'Elia

State University of New York System

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Hans W. Paerl

University of North Carolina at Chapel Hill

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W. M. Kemp

University System of Maryland

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Alan F. Blumberg

Stevens Institute of Technology

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