A modeling study of the dynamics of pore water seepage from intertidal marsh sediments

A numerical boundary integral equation model has been used to simulate tidally driven transient variations in pore water seepage from salt marsh sediments into tidal channels and its subsequent recharge by tidal inundation. In general the results show that the maximum seepage discharge occurs at or near the intersection of the creek bank and the channel water surface. Over a tidal cycle typically two-thirds of the total seepage discharge occurs through the creek bank with only about a third discharging from the channel bottom. Of the creek-bank discharge up to a third occurs through the seepage face that develops above the tide line at tidal stages below mean tide. These results indicate that placement of seepage meters only on the channel bottom will not give samples or measures representative of the total seepage. Of the total recharge only about 5% occurs through the upper part of the creek bank with the remainder infiltrating vertically through the marsh platform during early stages of tidal submergence. For the platform recharge about 80% occurs within 3 m of the creek bank. Thus, most of the water that seeps out of marsh sediments is derived from sediments that lie within several meters of the creek bank and accordingly has had a relatively short residence (one to two years) in the marsh. Compared to the distal portion of the marsh this relatively rapid flushing may enhance the productivity of Spartina alterniflora in the creek-bank environment and control the differential generation of radium quartet isotopes.     

A Lagrangian view of fluorescent chromophoric dissolved organic matter distributions in the Mississippi River plume

In April 2001, three instrumented surface drifters were deployed in the Mississippi River plume near the mouth of Southwest Pass. The plume was characterized by strong surface gradients of salinity, temperature, and chromophoric dissolved organic matter fluorescence (F_CDOM). The drifters initially headed west and attained peak speeds of 1 m s⁻¹ within 5 h after release. Thereafter, velocity decreased as the triad headed north in the Louisiana Bight. Linear relationships between F_CDOM and salinity identified two subsurface sources of high salinity water (salinity >35) underlying the surface plume. The platforms stalled in a surface front about 40 h after deployment, and then slowly drifted south along the eastern perimeter of the plume. Shoreward of the plume front there were patches of low-salinity, high F_CDOM ‘patches’ of surface waters that likely originated in the marshes, bayous, and other smaller distributaries of the delta.     

Seasonal evolution of hydrographic properties in the Antarctic circumpolar current at 170°W during 1997–1998

This paper discusses the seasonal evolution of the hydrographic and biogeochemical properties in the Antarctic Circumpolar Current (ACC) during the US Joint Global Ocean Flux (JGOFS) Antarctic Environment and Southern Ocean Process Study (AESOPS) in 1997–1998. The location of the study region south of New Zealand along 170°W was selected based on the zonal orientation and meridional separation of the physical and chemical fronts found in that region. Here we endeavor to describe the seasonal changes of the macronutrients, fluorescence chlorophyll_, particulate organic carbon (POC), and carbon dioxide (CO₂) in the upper 400 m of the ACC during the evolution of the seasonal phytoplankton bloom found in this area. While the ACC has extreme variability in the meridional sense (due to fronts, etc.), it appears to be actually quite uniform in the zonal sense. This is reflected by the fact that a good deal of the seasonal zonal changes in nutrients distributions at 170°W follow a pattern that reflects what would be expected if the changes are associated with seasonal biological productivity. Also at 170°W, the productivity of the upper waters does not appear to be limited by availability of phosphate or nitrate. While there is a significant decrease (or uptake) of inorganic nitrogen, phosphate and silicate associated with the seasonal phytoplankton bloom, none of the nutrients, except perhaps silicate (north of the silicate front) are actually depleted within the euphotic zone. At the end of the growing season, nutrient concentrations rapidly approached their pre-bloom levels. Inspection of the ratios of apparent nutrient drawdown near 64°S suggests N/P apparent drawdowns to have a ratio of 10 and N/Si apparent drawdowns to have a ratio of >4. These ratios suggest a bloom that was dominated by Fe limited diatoms. In addition, the surface water in the Polar Front (PF) and the Antarctic Zone (AZ) just to the south of the PF take up atmospheric CO₂ at a rate 2–3 times as fast as the mean global ocean rate during the summer season but nearly zero during the rest of year. This represents an important process for the transport of atmospheric CO₂ into the deep ocean interior. Finally, the net CO₂ utilization or the net community production during the 2.5 growing months between the initiation of phytoplankton blooms and mid-January increase southward from 1.5 mol C m⁻² at 55°S to 2.2 mol C m⁻² to 65°S across the Polar Frontal Zone (PFZ) into the AZ.     

Sediment Nitrogen Fixation: a Call for Re-evaluating Coastal N Budgets

Coastal ocean primary productivity is often limited by nitrogen (N) availability, which is determined by the balance between N sources (e.g., N-fixation, groundwater, river inputs, etc.) and sinks (e.g., denitrification, sediment burial, etc.). Historically, heterotrophic N-fixation in sediments was excluded as a significant source of N in estuarine budgets, based on low, indirectly measured rates (e.g., acetylene reduction assay) and because it was unnecessary to achieve mass balance. Many recent studies using net N₂ flux measurements have shown that sediment N-fixation can equal or exceed N₂ loss. In an effort to quantify N₂ production and consumption simultaneously, we measured N-fixation and denitrification directly in sediment cores from a temperate estuary (Waquoit Bay, MA). N-fixation, dissimilatory nitrate reduction to ammonium, and denitrification occurred simultaneously, and the net N₂ flux shifted from uptake (N-fixation) to efflux (denitrification) over the 120-h incubation. Evidence for N-fixation included net ²⁸N₂ and ³⁰N₂ uptake, ¹⁵NH₄ ⁺ production from ³⁰N₂ additions, ¹⁵N_{organic matter} production, and nifH expression. N-fixation from ³⁰N₂ was up to eight times higher than potential denitrification. However, N-fixation calculated from ¹⁵NO₃ ^? was one half of the measured fixation from ³⁰N₂, indicating that ¹⁵NO₃-isotope labeling calculations may underestimate N-fixation. These results highlight the dynamic nature of sediment N cycling and suggest that quantifying individual processes allows a greater understanding of what net N₂ fluxes signify and how that balance varies over time.     

Geochemistry and isotopes of fluids from sulphur springs, Valles Caldera, New Mexico

Detailed geochemistry supported by geologic mapping has been used to investigate Sulphur Springs, an acid-sulfate hot spring system that issues from the western flank of the resurgent dome inside Valles Caldera. The most intense activity occurs at the intersection of faults offsetting caldera-fill deposits and post-caldera rhyolites. Three geothermal wells in the area have encountered pressures <1 MPa and temperatures of 200°C at depths of 600 to 1000 m. Hot spring and fumarole fluids may discharge at boiling temperatures with pH 1.0 and SO₄ 8000 mg/l. These conditions cause argillic alterations throughout a large area.Non-condensible gases consist of roughly 99% CO₂ with minor amounts of H₂S, H₂, and CH₄. Empirical gas geothermometry suggests a deep reservoir temperature of 215 to 280°C. Comparison of ¹³C and ¹⁸O between CaCO₃ from well cuttings and CO₂ from fumarole steam indicates a fractionation temperature between 200 and 300°C by decarbonation of hydrothermally altered Paleozoic limestone and vein calcite in the reservoir rocks. Tritium concentrations obtained from steam condensed in a mudpot and deep reservoir fluids (Baca #13, 278°C) are 2.1 and 1.0 T.U. respectively, suggesting the steam originates from a reservoir whose water is mostly >50 yrs old. Deuterium contents of fumarole steam, deep reservoir fluid, and local meteoric water are practically identical even though ¹⁸O contents range through 4‰, thus, precipitation on the resurgent dome of the caldera could recharge the hydrothermal system by slow percolation. From analysis of D and ¹⁸O values between fumarol steam and deep reservoir fluid, steam reaches the surface either (1) by vaporizing relatively shallow groundwater at 200°C or (2) by means of a two-stage boiling process through an intermediate level reservoir at roughly 200°C.Although many characteristics of known vapor-dominated geothermal systems are found at Sulphur Springs, fundamental differences exist in temperature and pressure of our postulated vapor-zone. We propose that the reservoir beneath Sulphur Springs is too small or too poorly confined to sustain a “true” vapor-dominated system and that the Sulphur Springs system may be a “dying” vapor-dominated system that has practically boiled itself dry.     

Isovolumetric geochemical investigation of a buried granite saprolite near Columbia,SC, U.S.A.

Saprolites are residual soils which preserve the textures of their parent rocks and thus have evolved by an isovolumetric process of weathering (MILLOT, 1970, The Geology of Clays, Springer). Using bulk density, saprolite elemental analyses can be converted to units of g cm^?3. Furthermore, an empirical reaction progress diagram can be constructed for a suite of saprolite samples by plotting element concentrations (in g cm^?3) against bulk density (B.D.). Our data for a granite saprolite show that Al₂O₃ and SiO₂ decrease in a linear fashion from B.D. 2.1g cm^?3 to 1.5g cm^?3 but that K₂O follows a curvilinear trend such that it decreases from 75% of its fresh rock value at B.D. 1.6 g cm^?3 to nearly zero at B.D. 1.5 g cm^?3. The only hypothetical reaction paths that are compatible with these B.D. vs A1₂O₃, SiO₂ and K₂O constraints are those in which orthoclase alters to kaolinite through an intermediate potassium phase similar to KAl₃Si₃O₁₀(OH)₂ or KAl₂Si₂O₆(OH)₃ (hypothetical K-kaolinite). Normative mineral calculations, X-ray diffraction data and structural H₂O data are employed to test this conclusion.     

The olivine-plagioclase reaction: Geological evidence from the seiland petrographic province,northern Norway

The experimentally determined equilibrium curves for the subsolidus olivineplagioclase reaction fall into two groups: those with positive slopes (dP/dT) that suggest reaction during cooling, and those with zero slopes that imply reaction by increase of pressure. Corona structures were developed in the mafic cumulates of northern Norway at different times during Caledonian almandine amphibolite facies metamorphism, as individual intrusions cooled from solidus temperatures. Unless pressure increases coincided fortuitously with subsolidus cooling, these relationships suggest that the positive-slope models are most analogous to natural systems.     

A sediment trap intercomparison study in the Santa Barbara Basin

Four sediment traps of radically different design were deployed in the Santa Barbara Basin for approximately 45 days. The measured fluxes ranged from 370 to 774 g m^?2 yr^?1 for the different designs. These values lie within flux measurements previously determined for the basin. Compared to the 25-year record (920 g m^?2 yr^?1), however, all fluxes determined in this experiment are somewhat low. Because this experiment was conducted during a general period of high storm activity and runoff, measurement of greater than average flux was expected. It is probable that the higher flux recorded by the sediments results from a significant input of detritus into the basin by near bottom transport.The chemical composition of trapped material was nearly identical in all four trap designs. The deep cone design, however, had a significantly lower Mn content. Since this trap was the only one in which reducing conditions were produced in the sample container, reduction and mobilization of manganese after collection is believed to have occurred.In spite of the very different designs tested, the factor of two agreement in flux determination and the compositional similarity of the material collected is encouraging for future attempts to directly measure the flux of particulates in the ocean.     

The effects of sea salts on the forms of nitrogen released from estuarine and freshwater sediments: Does ion pairing affect ammonium flux?

In sediments with oxidized surface layers, the percentage of mineralized nitrogen that is nitrified/denitrified, compared with that released directly as ammonium, appears to be affected by the presence of sea salts. In estuarine systems, a significant portion of the nitrogen is released as ammonium, whereas in freshwater systems, most of the mineralized nitrogen is often released from the sediments as nitrogen gas. We hypothesized that this discrepancy is caused by differential competition between physical diffusion and nitrification/denitrification in the two systems. The vertical migration (by Fickian diffusion) of ammonium out of the oxic layer may be hindered by cation exchange (or sorption) interactions with sediment particles to a greater extent in fresh water than in estuarine systems. The resulting relatively long residence time, and potentially high levels of particle-bound ammonium in the freshwater sediments, would favor nitrification as the major ammonium removal process. By contrast, ion pair formation of ammonium with seawater anions and blockage of sediment cation exchange sites with seawater cations may allow a sizable fraction of the ammonium to diffuse out of estuarine sediments before it is nitrified. A salt effect, consistent with this hypothesis, has been demonstrated in experimental systems by changing the ionic composition of water flowing above intact cores of freshwater and estuarine sediments. Steady-state ammonium release from Lake Michigan sediments was substantially enhanced in the presence of 30% seawater over that in the presence of lake water alone. Likewise, steady-state ammonium release, from Ochlockonee River and Bay sediments (Florida) and from Toms River and Barnegat Bay sediments (New Jersey), was usually higher in the presence of diluted synthetic seawater than it was in the presence of fresh water.     

Time series analyses of suspended sediment concentrations at North Inlet,South Carolina

Daily water samples have been collected at three stations in the North Inlet (South Carolina) marshestuary system since February 1981 as part of the NSF Long-Term Ecological Research (LTER) project. As a result of this sampling regime, nearly continuous time series of inorganic and organic suspended sediment, particulate organic carbon (POC), Secchi disk, salinity, and water temperature are now available. Power spectrum analysis of these data reveals that most of the explainable variance in the inorganic suspended sediment, POC, and Secchi disk data is related to a yearly cycle that is strongly coherent with water temperature such that high turbidity is associated with high water temperature. Only a small fraction of the explainable variance is associated with frequencies that can be related to the semidiurnal tide. Simple correlation analysis also indicates that turbidity is more closely associated with water temperature than with tide height or salinity. The ratio of POC to inorganic suspended sediment shows no discernible power spectra peaks and is weakly, but inversely, correlated with temperature. From these results we hypothesize that temperature-regulated bioturbation is the main factor controlling turbidity variations in the system. The lack of a strong inverse correlation between turbidity and salinity suggests that river runoff has little immediate impact on the suspended sediment of nearshore coastal waters in systems similar to North Inlet.