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Carol Kendall

Publications and source records attributed to Carol Kendall.

At least 55 records · Page 3Linked to original sources

Variability of isotope and major ion chemistry in the Allequash Basin, Wisconsin

As part of ongoing research conducted at one of the U.S. Geological Survey's Water, Energy, and Biogeochem-ical Budgets sites, work was undertaken to describe the spatial and temporal variability of stream and ground water isotopic composition and cation chemistry in the Trout Lake watershed, to relate the variability to the watershed flow system, and to identify the linkages of geochemical evolution and source of water in the watershed. The results are based on periodic sampling of sites at two scales along Allequash Creek, a small headwater stream in northern Wisconsin. Based on this sampling, there are distinct water isotopic and geochemical differences observed at a smaller hillslope scale and the larger Allequash Creek scale. The variability was larger than expected for this simple watershed, and is likely to be seen in more complex basins. Based on evidence from multiple isotopes and stream chemistry, the flow system arises from three main source waters (terrestrial-, lake-, or wetland-derived recharge) that can be identified along any flowpath using water isotopes together with geochemical characteristics such as iron concentrations. The ground water chemistry demonstrates considerable spatial variability that depends mainly on the flow-path length and water mobility through the aquifer. Calcium concentrations increase with increasing flowpath length, whereas strontium isotope ratios increase with increasing extent of stagnation in either the unsaturated or saturated zones as waters move from source to sink. The flowpath distribution we identify provides important constraints on the calibration of ground water flow models such as that undertaken by Pint et al. (this issue).

Wisconsin↗

The geochemical evolution of riparian ground water in a forested piedmont catchment

The principal weathering reactions and their rates in riparian ground water were determined at the Panola Mountain Research Watershed (PMRW) near Atlanta, Georgia. Concentrations of major solutes were measured in ground water samples from 19 shallow wells completed in the riparian (saprolite) aquifer and in one borehole completed in granite, and the apparent age of each sample was calculated from chloroflourocarbons and tritium/helium-3 data. Concentrations of SiO 2 , Na + , and Ca 2+ generally increased downvalley and were highest in the borehole near the watershed outlet. Strong positive correlations were found between the concentrations of these solutes and the apparent age of ground water that was modern (zero to one year) in the headwaters, six to seven years midway down the valley, and 26 to 27 years in the borehole, located ∼500 m downstream from the headwaters. Mass-balance modeling of chemical evolution showed that the downstream changes in ground water chemistry could be largely explained by weathering of plagioclase to kaolinite, with possible contributions from weathering of K-feldspar, biotite, hornblende, and calcite. The in situ rates of weathering reactions were estimated by combining the ground water age dates with geochemical mass-balance modeling results. The weathering rate was highest for plagioclase (∼6.4 μmol/L/year), but could not be easily compared with most other published results for feldspar weathering at PMRW and elsewhere because the mineral-surface area to which ground water was exposed during geochemical evolution could not be estimated. However, a preliminary estimate of the mineral-surface area that would have contacted the ground water to provide the observed solute concentrations suggests that the plagioclase weathering rate calculated in this study is similar to the rate calculated in a previous study at PMRW, and three to four orders of magnitude slower than those published in previous laboratory studies of feldspar weathering. An accurate model of the geochemical evolution of riparian ground water is necessary to accurately model the geochemical evolution of stream water at PMRW.

Groundwater↗

Characterization of surface and ground water δ18O seasonal variation and its use for estimating groundwater residence times

18 O is an ideal tracer for characterizing hydrological processes because it can be reliably measured in several watershed hydrological compartments. Here, we present multiyear isotopic data, i.e. 18 O variations (δ 18 O), for precipitation inputs, surface water and groundwater in the Shingobee River Headwaters Area (SRHA), a well-instrumented research catchment in north-central Minnesota. SRHA surface waters exhibit δ 18 O seasonal variations similar to those of groundwaters, and seasonal δ 18 O variations plotted versus time fit seasonal sine functions. These seasonal δ 18 O variations were interpreted to estimate surface water and groundwater mean residence times (MRTs) at sampling locations near topographically closed-basin lakes. MRT variations of about 1 to 16 years have been estimated over an area covering about 9 km 2 from the basin boundary to the most downgradient well. Estimated MRT error (±0·3 to ±0·7 years) is small for short MRTs and is much larger (±10 years) for a well with an MRT (16 years) near the limit of the method. Groundwater transit time estimates based on Darcy's law, tritium content, and the seasonal δ 18 O amplitude approach appear to be consistent within the limits of each method. The results from this study suggest that use of the δ 18 O seasonal variation method to determine MRTs can help assess groundwater recharge areas in small headwaters catchments.

Minnesota↗

Freshwater and saline loads of dissolved inorganic nitrogen to Hood Canal and Lynch Cove, western Washington

Hood Canal is a long (110 kilometers), deep (175 meters) and narrow (2 to 4 kilometers wide) fjord of Puget Sound in western Washington. The stratification of a less dense, fresh upper layer of the water column causes the cold, saltier lower layer of the water column to be isolated from the atmosphere in the late summer and autumn, which limits reaeration of the lower layer. In the upper layer of Hood Canal, the production of organic matter that settles and consumes dissolved oxygen in the lower layer appears to be limited by the load of dissolved inorganic nitrogen (DIN): nitrate, nitrite, and ammonia. Freshwater and saline loads of DIN to Hood Canal were estimated from available historical data. The freshwater load of DIN to the upper layer of Hood Canal, which could be taken up by phytoplankton, came mostly from surface and ground water from subbasins, which accounts for 92 percent of total load of DIN to the upper layer of Hood Canal. Although DIN in rain falling on land surfaces amounts to about one-half of the DIN entering Hood Canal from subbasins, rain falling directly on the surface of marine waters contributed only 4 percent of the load to the upper layer. Point-source discharges and subsurface flow from shallow shoreline septic systems contributed less than 4 percent of the DIN load to the upper layer. DIN in saline water flowing over the sill into Hood Canal from Admiralty Inlet was at least 17 times the total load to the upper layer of Hood Canal. In September and October 2004, field data were collected to estimate DIN loads to Lynch Cove - the most inland marine waters of Hood Canal that routinely contain low dissolved-oxygen waters. Based on measured streamflow and DIN concentrations, surface discharge was estimated to have contributed about one-fourth of DIN loads to the upper layer of Lynch Cove. Ground-water flow from subbasins was estimated to have contributed about one-half of total DIN loads to the upper layer. In autumn 2004, the relative contribution of DIN from shallow shoreline septic systems to the upper layer was higher in Lynch Cove (23 percent) than in the entire Hood Canal. Net transport of DIN into Lynch Cove by marine currents was measured during August and October 2004-a time of high biological productivity. The net transport of lower-layer water into Lynch Cove was significantly diminished relative to the flow entering Hood Canal at its entrance. Even though the net transport of saline water into the lower layer of Lynch Cove was only 119 cubic meters per second, estuarine currents between 33 and 47 m were estimated to have carried more than 35 times the total freshwater load of DIN to the upper layer from surface and ground water, shallow shoreline septic systems, and direct atmospheric rainfall. The subsurface maximums in measured turbidity, chlorophyll a, particulate organic carbon, and particulate organic nitrogen strongly suggest that the upward mixing of nitrate-rich deeper water is a limiting factor in supplying DIN to the upper layer that enhances marine productivity in Lynch Cove. The presence of phosphate in the upper layer in the absence of dissolved inorganic nitrogen also suggests that the biological productivity that leads to low dissolved-oxygen concentrations in the lower layer of Lynch Cove is limited by the supply of nitrogen rather than by phosphate loads. Although the near-shore zones of the shallow parts of Lynch Cove were sampled, a biogeochemical signal from terrestrial nitrogen was not found. Reversals in the normal estuarine circulation suggest that if the relative importance of the DIN load of freshwater terrestrial and atmospheric sources and the DIN load from transport of saline water by the estuarine circulation in controlling dissolved-oxygen concentrations in Lynch Cove is to be better understood, then the physical forces driving Hood Canal circulation must be better defined.

Scientific Investigations Report↗

Tracing sources of streamwater sulfate during snowmelt using S and O isotope ratios of sulfate and 35S activity

The biogeochemical cycling of sulfur (S) was studied during the 2000 snowmelt at Sleepers River Research Watershed in northeastern Vermont, USA using a hydrochemical and multi-isotope approach. The snowpack and 10 streams of varying size and land use were sampled for analysis of anions, dissolved organic carbon (DOC), 35 S activity, and δ 34 S and δ 18 O values of sulfate. At one of the streams, δ 18 O values of water also were measured. Apportionment of sulfur derived from atmospheric and mineral sources based on their distinct δ 34 S values was possible for 7 of the 10 streams. Although mineral S generally dominated, atmospheric-derived S contributions exceeded 50% in several of the streams at peak snowmelt and averaged 41% overall. However, most of this atmospheric sulfur was not from the melting snowpack; the direct contribution of atmospheric sulfate to streamwater sulfate was constrained by 35 S mass balance to a maximum of 7%. Rather, the main source of atmospheric sulfur in streamwater was atmospheric sulfate deposited months to years earlier that had microbially cycled through the soil organic sulfur pool. This atmospheric/pedospheric sulfate (pedogenic sulfate formed from atmospheric sulfate) source is revealed by δ 18 O values of streamwater sulfate that remained constant and significantly lower than those of atmospheric sulfate throughout the melt period, as well as streamwater 35 S ages of hundreds of days. Our results indicate that the response of streamwater sulfate to changes in atmospheric deposition will be mediated by sulfate retention in the soil.

Vermont↗

Effects of suburban development on runoff generation in the Croton River basin, New York, USA

The effects of impervious area, septic leach-field effluent, and a riparian wetland on runoff generation were studied in three small (0.38–0.56 km 2 ) headwater catchments that represent a range of suburban development (high density residential, medium density residential, and undeveloped) within the Croton River basin, 70 km north of New York City. Precipitation, stream discharge, and groundwater levels were monitored at 10–30 min intervals for 1 year, and stream water and groundwater samples were collected biweekly for δ 18 O, NO 3 − , and SO 4 2− analysis for more than 2 years during an overlapping period in 2000–2002. Data from 27 storms confirmed that peak magnitudes increased and recession time decreased with increasing development, but lags in peak arrival and peak discharge/mean discharge were greatest in the medium density residential catchment, which contains a wetland in which storm runoff is retained before entering the stream. Baseflow during a dry period from Aug. 2001–Feb. 2002 was greatest in the high-density residential catchment, presumably from the discharge of septic effluent through the shallow groundwater system and into the stream. In contrast, moderate flows during a wet period from Mar.–Aug. 2002 were greatest in the undeveloped catchment, possibly as a result of greater subsurface storage or greater hydraulic conductivity at this site. The mean residence time of baseflow was about 30 weeks at all three catchments, indicating that human influence was insufficient to greatly affect the groundwater recharge and discharge properties that determine catchment residence time. These results suggest that while suburban development and its associated impervious surfaces and storm drains accelerate the transport of storm runoff into streams, the combined effects of remnant natural landscape features such as wetlands and human alterations such as deep groundwater supply and septic systems can change the expected effects of human development on storm runoff and groundwater recharge.

New York↗

Evaluating the source of streamwater nitrate using δ 15 N and δ 18 O in nitrate in two watersheds in New Hampshire, USA

The natural abundance of nitrogen and oxygen isotopes in nitrate can be a powerful tool for identifying the source of nitrate in streamwater in forested watersheds, because the two main sources of nitrate, atmospheric deposition and microbial nitrification, have distinct δ 18 O values. Using a simple mixing model, we estimated the relative fractions in streamwater derived from these sources for two forested watersheds with markedly different streamwater nitrate outputs. In this study, we monitored δ 15 N and δ 18 O of nitrate biweekly in atmospheric deposition and in streamwater for 20 months at the Hubbard Brook Experimental Forest, New Hampshire, USA (moderate nitrogen export), and monthly in streamwater at the Bowl Research Natural Area, New Hampshire, USA (high nitrogen export). For rain, δ 18 O values ranged from +47 to +77‰ (mean: +58‰) and δ 15 N from −5 to +1‰ (mean: −3‰); for snow, δ 18 O values ranged from +52 to +75‰ (mean: +67‰) and δ 15 N from −3 to +2‰ (mean: −1‰). Streamwater nitrate, in contrast to deposition, had δ 18 O values between +12 and +33‰ (mean: +18‰) and δ 15 N between −3 and +6‰ (mean: 0‰). Since nitrate produced by nitrification typically has δ 18 O values ranging from −5 to +15‰, our field data suggest that most of the nitrate lost from the watersheds in streamflow was nitrified within the catchment. Our results confirm the importance of microbial nitrogen transformations in regulating nitrogen losses from forested ecosystems and suggest that hydrologic storage may be a factor in controlling catchment nitrate losses.

Hydrological Processes↗

Scale effects on headwater catchment runoff timing, flow sources, and groundwater‐streamflow relations

The effects of catchment size and landscape organization on runoff generation are poorly understood. Little research has integrated hillslope and riparian runoff investigation across catchments of different sizes to decipher first‐order controls on runoff generation. We investigated the role of catchment sizes on riparian and hillslope dynamics based on hydrometric and tracer data observed at five scales ranging from trenched hillslope sections (55–285 m 2 ) to a 280‐ha catchment at Maimai on the west coast of the South Island, New Zealand. The highly organized landscape is comprised of similar headwater catchments, regular geology, steep highly dissected topography, relatively consistent soil depths, and topographically controlled shallow through flow. We found a strong correlation between riparian zone groundwater levels and runoff for the headwaters, whereas the water tables in the valley bottom of the larger catchments were uncorrelated to runoff for 14 months of record. While there was no clear relationship between catchment size and new water contribution to runoff in the two storms analyzed in detail, lag times of tracer responses increased systematically with catchment size. The combination of hydrometric and tracer data allowed assessment of the runoff contributions from different parts of the landscape. Runoff was generated consistently in headwater riparian zones. This agreed also with the observed variations of tracer ( 18 O and silica) responses for the different catchments. During wetter antecedent conditions or during larger events (>30 mm under dry antecedent conditions) hillslope and valley bottom floodplains did contribute to event runoff directly. We propose that analysis of landscape‐scale organization and the distribution of dominant landscape features provide a structure for investigation of runoff production and solute transport, especially as catchment‐scale increases from headwaters to the mesoscale.

Water Resources Research↗

Stable Isotope Analysis of Water and Aqueous Solutions by Conventional Dual-Inlet Mass Spectrometry

This chapter reviews the recent developments and refinements of analytical methods for preparing waters and other aqueous samples of different origins for the measurement of the oxygen and hydrogen isotopes by conventional dual-inlet, dynamic gas-source isotope-ratio mass spectrometry. The emerging techniques of continuous-flow mass-spectrometry are discussed as they are employed in both dual-inlet and continuous-flow mass-spectrometry. The size, chemical composition, and isotopic abundance of aqueous samples vary widely depending on their type, origin, and history. Automated gas equilibration methods are very suitable and are becoming standard techniques in many isotope hydrology laboratories. The increased analytical precisions are due to the subsequent development of modern gas-source isotope-ratio mass spectrometers with dual-inlets and multi-collectors, have caused the proliferation of new analytical methods and applications for the oxygen and hydrogen isotopic compositions of water. For natural hydrologic samples and new developments of continuous-flow mass spectrometry, it is possible to determine both δD and δ 18 O values, as they can provide two-dimensional information. The most significant progress in analytical techniques for stable isotope analysis of water is witnessed. Hence, overall quality control of isotopic data is becoming an important issue.

Book chapter↗

Preparation and analysis of nitrogen-bearing compounds in water for stable isotope ratio measurement

This chapter reviews methods for analyzing "natural abundance" nitrogen-bearing compounds in water for δ 15 N, δ 18 O, and δ 17 O. The techniques that are reviewed are Kjeldahl distillation and digestion, diffusion, micro diffusion, ion exchange, and microbial denitrifier methods. It overlaps the contents of the preparation of ecological and biogeochemical samples for isotope analysis and also covers sections on particulate organic nitrogen and biological samples. Nitrogen comprises 78% of the atmosphere, oxygen 21% and argon 1%. There are two stable isotopes of N are 14 N and 15 N and a wide range of oxidation numbers exhibited by nitrogen compounds. Developments of continuous-flow mass spectrometry makes it possible to determine both δ15N and δ18O values of nitrate samples. Such techniques are particularly useful for small-size samples. With decreasing sample size, possible isotopic fractionations associated with extraction from the matrix, contaminants in the reagents, and leaks will become more significant. Due to the interest in distinguishing different species of organic-N compounds, the diffusion method is applied to differentiate types of organic-N.

Book chapter↗

Isotopic views of food web structure in the Florida Everglades

Introduction Nearly one million acres of the Everglades are under a health advisory that discourages the human consumption of largemouth bass and several other fish because of high mercury contents. Food web structure (base of food web, number of trophic steps) plays a potentially critical role in determining the patterns of mercury contamination of the Everglades ecosystem. Methylmercury (MeHg) is present in low concentrations in water, yet after entering the base of the food web it biomagnifies to toxic concentrations in organisms that occupy higher trophic positions (like bass). One of the main research questions under investigation by a multi-agency task force in the Everglades is how MeHg bioaccumulates up the food chain in this complex aquatic ecosystem. Understanding variations in food web structure may help explain mercury patterns in the Everglades and ultimately lead to more effective restoration of Everglades ecosystems.

Florida↗

Sources and Transport of Nutrients, Organic Carbon, and Chlorophyll-a in the San Joaquin River Upstream of Vernalis, California, during Summer and Fall, 2000 and 2001

Oxidizable materials from the San Joaquin River upstream of Vernalis can contribute to low dissolved oxygen episodes in the Stockton Deep Water Ship Channel that can inhibit salmon migration in the fall. The U.S. Geological Survey collected and analyzed samples at four San Joaquin River sites in July through October 2000 and June through November 2001, and at eight tributary sites in 2001. The data from these sites were supplemented with data from samples collected and analyzed by the University of California at Davis at three San Joaquin River sites and eight tributary sites as part of a separate study. Streamflows in the San Joaquin River were slightly above the long-term average in 2000 and slightly below average in 2001. Nitrate loads at Vernalis in 2000 were above the long-term average, whereas loads in 2001 were close to average. Total nitrogen loads in 2000 were slightly above average, whereas loads in 2001 were slightly below average. Total phosphorus loads in 2000 and 2001 were well below average. These nutrient loads correspond with the flow-adjusted concentration trends--nitrate concentrations significantly increased since 1972 (p < 0.01), whereas total nitrogen and total phosphorus concentrations did not (p > 0.05). Loading rates of nutrients and dissolved organic carbon increased in the San Joaquin River in the fall with the release of wetland drainage into Mud Slough and with increased reservoir releases on the Merced River. During August 2000 and September 2001, the chlorophyll-a loading rates and concentrations in the San Joaquin River declined and remained low during the rest of the sampling period. The most significant tributary sources of nutrients were the Tuolumne River, Harding Drain, and Mud Slough. The most significant tributary sources of dissolved organic carbon were Salt Slough, Mud Slough, and the Tuolumne and Stanislaus Rivers. Compared with nutrients and dissolved organic carbon, the tributaries were minor sources of chlorophyll-a, suggesting that most of the chlorophyll-a was produced in the San Joaquin River rather than its tributaries. On the basis of the carbon-to-nitrogen ratios and the d13C of particulate organic matter in the San Joaquin River and tributaries, the particulate organic matter in the river was mostly phytoplankton. On the basis of the d15N values of the particulate organic matter, and of total dissolved nitrogen and nitrate, the nitrate in the San Joaquin River probably was a significant nutrient source for the phytoplankton. The range of d15N and d18O values of nitrate in the San Joaquin River and tributaries suggest that animal waste or sewage was a significant source of nitrate in the river at the time the samples were collected.

Water-Resources Investigations Report↗

Shallow water table fluctuations in relation to soil penetration resistance

Hydrologic modeling of catchments is frequently hampered by lack of information on subsurface stratigraphy and zones of preferred flow. We evaluated the usefulness of soil penetration resistance, easily measured by a dynamic cone penetrometer, together with measurements of ground water level fluctuations, as a cost-effective means to infer subsurface flow patterns. At our field site at Sleepers River, Vermont, penetration resistance was lowest in the surficial 10 to 30 cm, then typically increased to a local maximum at 60 to 80 cm, which we interpreted as the soil/till interface. Below this depth usually lies a zone of decreased resistance in the till, giving way to either a gradual or abrupt increase in resistance toward the bedrock surface at 1 to 4.5 m depth. Penetration resistance had a weak but significant negative correlation with saturated hydraulic conductivity determined by bail tests (r 2 = 0.25, p < 0.05). At many wells, monthly ground water levels tended to cluster at or just above the resistant zone near the soil/till interface. Chemical and isotopic dynamics in nested wells finished above and below the resistant zone suggest that the zone may temporarily isolate the deeper ground water reservoir from meltwater inputs, which were clearly identified by low δ 18 O values. In ground water discharge zones, δ 18 O values tended to converge throughout the profile. In contrast, dissolved organic carbon (DOC) maintained a gradient of increasing concentration toward land surface, even in otherwise well-mixed waters, reflecting its rapid release from organic horizons. Understanding the effect of soil penetration resistance on ground water behavior may be useful in future catchment modeling efforts.

Vermont↗

Analysis of δ15N and δ18O to differentiate NO3− sources in runoff at two watersheds in the Catskill Mountains of New York

To quantify the movement of atmospheric nitrogen deposition through two forested watersheds in the Catskill Mountains of New York, dual‐isotope analysis (δ 15 N and δ 18 O) was used to differentiate NO 3 − derived from precipitation from NO 3 − derived by microbial nitrification and to quantify the contributions of these sources to NO 3 − in drainage waters. Samples of stream water, soil water, precipitation, snowmelt, and O‐horizon soil were collected during the March and April snowmelt period of 1994 and throughout an 18‐month period from August 1995 through February 1997. The mean δ 18 O‐NO 3 − value of precipitation was +50.5‰, whereas the mean values for stream water and soil water were +17.7‰ and +23.6‰, respectively. The mean δ 15 N‐NO 3 − of precipitation was −0.2‰, that of soil water was +1.4‰, and that of stream water was +2.3‰; these values showed greater overlap among the three different waters than did the δ 18 O‐NO 3 − values, indicating that δ 15 N‐NO 3 − was not as useful for source separation. Soil water δ 18 O‐NO 3 − values decreased, and δ 15 N‐NO 3 − values increased, from the O to the B and C horizons, but most of the differences among horizons were not statistically significant. Nitrate derived by nitrification in incubated soil samples had a wide range of δ 15 N‐NO 3 − values, from +1.5‰ to +16.1‰, whereas δ 18 O‐NO 3 − values ranged more narrowly, from +13.2‰ to +16.0‰. Values of δ 18 O‐NO 3 − indicated that NO 3 − in stream water is mainly derived from nitrification. Only during a high‐flow event that exceeded the annual flood was precipitation a major contributor to stream water NO 3 − . Values of δ 18 O‐NO 3 − and δ 15 N‐NO 3 − changed at differing rates as NO 3 − cycled through these watersheds because δ 18 O‐NO 3 − values change sharply through the incorporation of oxygen from ambient water and gas during nitrification, whereas δ 15 N‐NO 3 − values change only incrementally through fractionation during biocycling processes. The results of this study show that most NO 3 − is first cycled through the biota and nitrified before entering the stream.

Water Resources Research↗

Pathways for nitrate release from an alpine watershed: Determination using δ15N and δ18O

Snowpack, snowmelt, precipitation, surface water, and groundwater samples from the Loch Vale watershed in Colorado were analyzed for δ 15 N and δ 18 O of nitrate to determine the processes controlling the release of atmospherically deposited nitrogen from alpine and subalpine ecosystems. Although overlap was found between the δ 15 N (NO3) values for all water types (−4 to +6‰), the δ 18 O (NO3) values for surface water and groundwater (+10 to +30‰) were usually distinct from snowpack, snowmelt, and rainfall values (+40 to +70‰). During snowmelt, δ 18 O (NO3) indicated that about half of the nitrate in stream water was the product of microbial nitrification; at other times that amount was greater than half. Springs emerging from talus deposits had high nitrate concentrations and a seasonal pattern in δ 18 O (NO3) that was similar to the pattern in the streams, indicating that shallow groundwater in talus deposits is a likely source of stream water nitrate. Only a few samples of surface water and groundwater collected during early snowmelt and large summer rain events had isotopic compositions that indicated most of the nitrate came directly from atmospheric deposition with no biological assimilation and release. This study demonstrates the value of the nitrate double‐isotope technique for determining nitrogen‐cycling processes and sources of nitrate in small, undisturbed watersheds that are enriched with inorganic nitrogen.

Water Resources Research↗

Chemical and isotopic evidence of nitrogen transformation in the Mississippi River, 1997-98

Nitrate (NO 3 ) and other nutrients discharged by the Mississippi River are suspected of causing a zone of depleted dissolved oxygen (hypoxic zone) in the Gulf of Mexico each summer. The hypoxic zone may have an adverse affect on aquatic life and commercial fisheries. The amount of NO 3 delivered by the Mississippi River to the Gulf of Mexico is well documented, but the relative contributions of different sources of NO 3 , and the magnitude of subsequent in-stream transformations of NO 3 , are not well understood. Forty-two water samples collected in 1997 and 1998 at eight stations located either on the Mississippi River or its major tributaries were analysed for NO 3 , total nitrogen (N), atrazine, chloride concentrations and NO 3 stable isotopes (δ 15 N and δ 18 O). These data are used to assess the magnitude and nature of in-stream N transformation and to determine if the δ 15 N and δ 18 O of NO 3 provide information about NO 3 sources and transformation processes in a large river system (drainage area 2 900 000 km 2 ) that would otherwise be unavailable using concentration and discharge data alone. Results from 42 samples indicate that the δ 15 N and δ 18 O ratios between sites on the Mississippi River and its tributaries are somewhat distinctive, and vary with season and discharge rate. Of particular interest are two nearly Lagrangian sample sets, in which samples from the Mississippi River at St Francisville, LA, are compared with samples collected from the Ohio River at Grand Chain, II, and the Mississippi River at Thebes, IL. In both Lagrangian sets, mass-balance calculations indicate only a small amount of in-stream N loss. The stable isotope data from the samples suggest that in-stream N assimilation and not denitrification accounts for most of the N loss in the lower Mississippi River during the spring and early summer months.

Illinois, Iowa, Kentucky, Louisiana, Mississippi, ↗