Fluxes of water, sediments, and biogeochemical compounds in salt marshes
- First Online:
- Cite this article as:
- Fagherazzi, S., Wiberg, P.L., Temmerman, S. et al. Ecol Process (2013) 2: 3. doi:10.1186/2192-1709-2-3
- 8.6k Views
Tidal oscillations systematically flood salt marshes, transporting water, sediments, organic matter, and biogeochemical elements such as silica. Here we present a review of recent studies on these fluxes and their effects on both ecosystem functioning and morphological evolution of salt marshes. We reexamine a simplified model for the computation of water fluxes in salt marshes that captures the asymmetry in discharge between flood and ebb. We discuss the role of storm conditions on sediment fluxes both in tidal channels and on the marsh platform. We present recent methods and field instruments for the measurement of fluxes of organic matter. These methods will provide long-term data sets with fine temporal resolution that will help scientists to close the carbon budget in salt marshes. Finally, the main processes controlling fluxes of biogenic and dissolved silica in salt marshes are explained, with particular emphasis on the uptake by marsh macrophytes and diatoms.
The exchange of sediments, silica, and organic matter between terrestrial ecosystems and the ocean is an important theme in ecological and biogeochemical studies. As a widely distributed coastal ecosystem covering 200,000–400,000 km2 globally, salt marshes are highly productive [net ecosystem production (NEP) = 1,585 g C m−2 year−1 ], rivaling tropical rainforests, due to abundant solar radiation, water, and nutrients provided by tidal water (Chmura et al. 2003; Duarte et al. 2005; Cai 2011). Tidal oscillations repeatedly flood salt marshes, giving rise to fluxes that bring water and constituents in and out of the system (Fagherazzi et al. 2012). This review focuses on fluxes of sediments, organic matter, and silica and their effects on both ecosystem functioning and morphological evolution of salt marshes. Particular attention is devoted to the feedbacks between physical and biological processes.
Salt marsh formation and persistence are dependent on the net flux of suspended sediment onto the marsh platform (Kirwan et al. 2010; Fagherazzi et al. 2012) and loss of salt marsh during storms (Mariotti and Fagherazzi 2010; Tonelli et al. 2010). Interactions between tidal flows and marsh vegetation promote deposition of sediment delivered to the marsh platform during flooding tides. Sediment deposition, along with accumulation of autochthonous organic material, contributes to the vertical accretion necessary for a marsh surface to maintain its elevation above mean sea level as sea level rises (Reed 1989; Morris et al. 2002; Mudd et al. 2009). Thus, healthy salt marshes must be net sediment sinks.
The buried carbon in the sediment of salt marshes as well as other intertidal wetlands, which is called “blue carbon,” is a significant carbon sink, sequestering in excess of 4.8–87.2 Tg C year−1 globally according to different estimations (Chmura et al. 2003; Duarte et al. 2005; McLeod et al. 2011). However, viewed in light of the global NEP of salt marshes of 634 Tg C year−1, only a small portion is retained in marsh sediments, and most of the produced biomass decomposes or is exported via lateral tidal fluxes (Middelburg et al. 1997; Duarte et al. 2005; Sharitz and Pennings 2006; Hopkinson et al. 2012).
In addition to carbon, other nutrients are deposited and recycled in coastal salt marshes. Of these, silicon (Si) is an essential element for primary production by diatoms in estuaries and coastal seas (Struyf and Conley 2009). In this paper we give an overview of studies that demonstrate the importance of tidal marshes in the associated estuarine Si cycle. In particular, we discuss the present state of knowledge regarding Si fluxes between tidal marshes and adjacent estuarine and coastal waters.
The paper is organized as follows: in the section “Fluxes of water,” we describe fluxes of water in salt marshes and put forward a simplified model for their computation. In “Fluxes of sediments,” we focus on fluxes of sediments both in tidal channels and on the marsh platform. In “Fluxes of organic material,” we discuss novel techniques to measure fluxes of organic matter, and in “Fluxes of silica,” we present a review of recent results on fluxes of silica in salt marshes. A set of conclusions and future research needs closes this review in the section “Conclusions.”
Fluxes of water
When tidal channels are not present, the transport of water between marsh and the surrounding coast occurs as a sheet flow on the marsh surface with very low water depths (French et al. 1995; Temmerman et al. 2005). This shallow flow favors the incision of creeks that, once scoured, capture more flow in a positive feedback that produces a network of dendritic channels dissecting the marsh platform (Fagherazzi and Furbish 2001; Fagherazzi and Sun 2004; D’Alpaos et al. 2005).
The water is thus carried to the marsh during flood and subsequently drained during ebb in two steps: during flood, the water first moves at relatively high speed in the channel network and then it spills on the platform (e.g., Christiansen et al. 2000; Davidson-Arnott et al. 2002; Temmerman et al. 2012). During ebb the opposite occurs, with the water first drained on the platform and then collected in the channels. As a result the morphology of the marsh and the distribution of channels have a strong influence on water fluxes.
where A(h) is the hypsometric curve (the surface flooded at each elevation h), Q is the discharge, and dh/dt the derivative of the tidal oscillation. Here for simplicity we assume that the water fluxes in and out of the marsh are concentrated in the channels, although a considerable volume of water is transported as sheet flow from the marsh edge directly on the marsh platform (French et al. 1995; Temmerman et al. 2005).
This equation is defined as the static model (tub model) and was first presented by Boon (1975). Since then it has been extensively used in salt marsh hydrodynamics (e.g., D’Alpaos et al. 2006,2007, 2010; Lawrence et al. 2004). This model implies that when there is a sharp increase in flooded area A, the discharge surges because more water is needed to flood a larger surface (or more water must be removed to drain it; see Figure 1B,C). As a result, two distinct surges are occurring in the channels, one when the marsh platform is first flooded and one when the marsh platform is drained. These surges have been measured in salt marsh channels by several authors (Myrick and Leopold 1963; Bayliss-Smith et al. 1978; Healey et al. 1981; French and Stoddart 1992).
The introduction of a delay in the static model of Boon (1975) does not considerably change the magnitude of the peak discharge but has a strong impact on velocities, which are obtained by dividing the discharge by water depth. If the ebb surge takes place at lower water depths, then the velocity increases, resulting in the characteristic ebb dominance of marsh creeks (Friedrichs and Aubrey 1988). Since bottom shear stress scales with the square of the velocity, this flow asymmetry favors erosion and incision during ebb.
Moreover, the distribution of travel times contains information about salt marsh morphology and related ecosystems. For example, deep channels with high drainage density reduce the travel time of water parcels, while thick halophyte vegetation on the marsh platform slows the flow (Mudd et al. 2004; Temmerman et al. 2007). In fact plant stems and leaves convert kinetic energy into turbulent kinetic energy, increasing drag and reducing flow velocity (Nepf 1999). Temmerman et al. (2012) showed that after cutting marsh vegetation over a relatively large area (4 ha) the flow velocity on the platform increased by a factor of 2 to 4, thus decreasing dramatically the travel time of water parcels.
Fluxes of sediments
In low marsh environments, where mineral sedimentation is greatest, daily tides inundate the marsh surface. Sediment suspended in the water flooding a low marsh can be the product of wave-driven resuspension in adjacent bays or tidally driven resuspension in tidal creeks.
Sediment fluxes in tidal channels
A storm surge therefore represents an ideal event for sediment input in a marsh (e.g., Cahoon 2006; Reed 1989; Turner et al. 2006): the strong wind associated with the storm produces waves that resuspend fine sediments in front of marshes, and the wind and wave setup increases the maximum tide level and thereby the water discharge during flood in the channels (by increasing the tidal prism; see Equations 1, 2). Therefore during a storm surge both discharge and sediment concentrations of the entering water are magnified, augmenting the total volume of sediment imported in the marsh (Equation 4).
This mechanism is well accepted in marsh studies, with several authors indicating storm conditions as ideal for marsh accretion (e.g., Reed 1989). However, sediment input during flood represents only half of the sediment budget. In fact sediments are exiting the marsh through the channels during the subsequent ebb flow. The same physics governs the export of sediments, and Equation 4 is still valid but now the integral is evaluated from thigh to tlow.
The main difference is that the sediment concentration of the exiting flow is now independent of the hydrodynamic conditions in the adjacent bays and tidal flats but is governed by physical processes mobilizing sediments within the salt marsh. Wind waves are negligible on marsh platforms, given the shallow water depths and the damping effect of vegetation (Möller et al. 1999). Therefore only tidal currents triggering high velocities are potentially responsible for sediment mobilization on the marsh surface during ebb, although field evidence seems to indicate that this effect is limited. Most of the sediment is therefore eroded and resuspended from the channels bottom and banks, where the velocities are high and vegetation does not protect the substrate. Data from Louisiana confirm that sediment concentration in the water exiting a marsh during ebb is proportional to the tidal velocity in the channel (Figure 5B) (Fagherazzi and Priestas 2010).
The discharge asymmetry outlined in the previous section enhances sediment erosion during ebb, since the peak in discharge occurs in the channels for shallow water depths thus augmenting flow velocity and bottom shear stresses (Figure 3). Storm surges are therefore excellent events also for the export of sediments, since all the water accumulated in the marsh during the surge will exit the system, giving rise to high ebb velocities and bottom stresses.
Moreover, given the low settling velocity of the fine material typical of marshlands, some of the sediment that was imported during flood might remain in suspension and exit the system during the following ebb. This is particularly true when the residence time of the water in the marsh is low, such as in marshes of small dimensions with a high drainage density (limited water paths), or when the water velocity is high and thus the travel time is short (large advection velocity). Again storm surges, by increasing flow velocities, decrease the likelihood of particle settling during high tide, reducing the potential accumulation of sediments on the marsh platform.
Best conditions for sediment accumulation are moderate storms that increase sediment resuspension near salt marshes, but don’t trigger fast flows in the channels (Fagherazzi and Priestas 2010). On the contrary, for sediment export the worst conditions occur during meteorological low tides (setdowns), when wind blows water away from the coastline and a large volume of water exits the marsh system. The setdown leads to shallow water depths, which, combined with large discharges, results in velocities that erode sediments in the channels. The low water levels also trigger large gradients in groundwater pressure leading to seepage and piping at channel banks (Gardner 2005; Howes and Goehringer 1994).
Sediment fluxes on the marsh platform
Regardless of how large the wave and tidal bed shear stresses are in the adjacent bays and creeks, interactions between the flow and marsh vegetation reduce the velocities and turbulence in the flooding flows within a short distance of entering the vegetation (Leonard and Luther 1995; Christiansen et al. 2000), creating conditions favorable for deposition of the sediment in suspension. In addition, reductions in near-bed velocities and drag around plant stems lead to skin friction stresses that are almost always insufficient to entrain sediment from the marsh surface. Therefore the dynamics of sediment transport on the marsh surface are dominated by slow advection during tidal inundation, accompanied by particle settling and interception by vegetation stems.
where ws is settling velocity, h is flow depth, Cs0 is initial concentration, t is time, x is distance from the creek bank or marsh edge, and U is average flow velocity on the marsh. Deposition rate is given by the divergence of sediment flux, −d(CsUh)/dx. It is clear from Equation 5 that concentration and hence deposition rate decrease along the flow path on the marsh platform and therefore with distance from the marsh edge (e.g., French et al. 1995; Leonard 1997; Reed et al. 1999; Temmerman et al. 2003). In fact the flow path on the marsh platform often coincides with the direction perpendicular to the marsh edge (Rinaldo et al. 1999; Marani et al. 2003). Peak flow velocities on the marsh surface tend to be small and do not vary much with tidal elevation or location on the marsh. Therefore settling velocity and flow depth are the primary controls of how much of the sediment entering the marsh is deposited.
These processes can be illustrated with an example from a microtidal (mean tidal range = 1.2 m) low marsh site in coastal Virginia, USA (Christiansen et al. 2000). Peak flow velocities at the site average ~0.2 cm/s during rising and falling tides. For tidal amplitudes between 0.95 and 1.05 m (hmax ≈ 0.6 m), average peak suspended sediment concentration entering the marsh platform during flood is 85 mg/L, which decreases by roughly 20% 3 m into the marsh (Christiansen et al. 2000). This rate of decrease is consistent with an average settling velocity of roughly 0.1 mm/s, the Stoke’s settling rate for particles of ~12 μm diameter. Grain size distributions of marsh surface sediment near the marsh edge have a modal size of 15–20 μm (Christiansen et al. 2000).
The apparent agreement between modal bed grain size and estimated settling rate indicated above proves somewhat misleading when size distribution and its evolution across the marsh surface are taken into consideration. First, analysis of size distribution indicates that 70–75% of the sediment deposited within 10 m of the creek bank is deposited as flocs (Christiansen et al. 2000). Second, there was no significant grain size fining with distance from the creek bank, as would be expected from a simple application of Equation 1 to a disaggregated grain size distribution. Only if deposition is dominated by flocs can the grain size distribution of deposited sediment remain largely unchanged along the flow path.
Voulgaris and Meyers (2004) measured settling velocities and particle characteristics in a tidal channel in South Carolina, USA, and on the adjacent marsh. They found that suspended particles in the channel were predominantly flocculated, with average settling velocities of about 0.1 mm/s during neap tides (mean diameter of 50 μm) and 0.25 mm/s during spring tides (estimated mean diameters of 50–150 μm) in the tidal channel and an average settling velocity of 0.24 mm/s on the marsh. Moskalski and Sommerfield (2012) measured particle characteristics on a salt marsh in Delaware and also found that flocs with median grain sizes of 50–150 μm predominated in marsh suspended sediment.
Wind-enhanced tidal and wave-generated bed shear stresses result in higher concentrations of suspended sediment in the water flooding the marsh (Christiansen et al. 2000; Lawson et al. 2007; Fagherazzi et al. 2010) and longer inundation times. As a result, deposition rates are higher and deposition extends further into the marsh during storm tides (e.g., Cahoon 2006; Reed 1989; Turner et al. 2006). For example, measured deposition near the creek bank at the Virginia coastal marsh site increased by roughly an order of magnitude during a period that included a significant northeaster (Christiansen 1998; Figure 6). At that site, northeasterly winds occurred during 11% of the tidal cycles but were estimated to contribute 27% of the annual deposition (Christiansen 1998).
Estimates of annual accretion based on short-term measurements of marsh deposition in the Virginia salt marsh site (~1 g cm−2 year−1, equivalent to about 1 cm/year assuming a bed porosity of about 0.65) exceed rates based on longer-term measurements (e.g., SETs) and rates of sea-level rise, suggesting that the marsh surface is subject to erosion as well as deposition (Christiansen 1998). Because bed shear stresses due to tidal flows on the marsh are too low to erode sediment, it is likely that erosion occurs via another process. Studies in a South Carolina marsh (Mwamba and Torres 2002; Torres et al. 2003) showed that rainfall can mobilize large quantities of sediment on a saturated, exposed marsh surface and suggest that low-tide rainfall runoff driven by marsh topography may be the primary erosional process on intertidal salt marshes.
Fluxes of organic material
In the past years several studies have focused on the storage of organic carbon in salt marshes (Morris and Bowden 1986; Chmura et al. 2003; Hussein et al. 2004; Choi and Wang 2004). Mudd et al. (2009) presents a combined framework including both refractory and labile organic fractions, as well as root growth and decay. The model shows that the amount of carbon stored in salt marshes depends on the competition between mineral sediment deposition and organic-matter accumulation. Direct warming of the marsh due to climate change favors aboveground vegetation production, while sea level rise leads to more accommodation space, thus increasing rates of carbon burial (Kirwan and Mudd 2012).
There is general consensus that lateral fluxes of organic carbon from salt marshes to the coastal ocean are significant (Childers et al. 2000; Odum 2000; Valiela et al. 2000). Globally, export of organic carbon from salt marshes ranges from 27 to 1,052 g C m−2 year−1 (Alongi 1998). Coastal geomorphology, geophysics, and hydrology are important determinants of organic matter exchange between coastal wetlands and estuaries (Bianchi 2007). In addition, from the perspective of stable isotope measurements and modeling, it has been shown that marsh DOC outwelling dominates particulate organic carbon (POC) outwelling (Eldridge and Cifuentes 2000). This conclusion is consistent with isotopic analysis suggesting that old, refractory organic carbon is dominant in riverine POC while salt marshes export more labile organic matter (Raymond and Bauer 2001; del Giorgio and Davis 2003).
Compared to quantitative studies of organic matter exchange between marsh and ocean, a small number of organic matter quality studies have been conducted so far. The quality of material flux could be interpreted as the identity (source) and functionality (fate) of the components within the pool of estuarine organic material. To identify the source of organic matter, researchers have used radioactive carbon and stable isotopic signatures of carbon, nitrogen, and sulfur (Peterson and Howarth 1987; Peterson et al. 1994; Raymond and Bauer 2001; Zhou et al. 2006), stoichiometry (Hopkinson and Vallino 2005; Lønborg et al. 2009), and biomarkers (Xu et al. 2006; Volkman et al. 2008). The studies of the fate of organic matter are based on biodegradability by using pyrolysis, gas chromatography–mass spectrometry (Hemminga et al. 1992, 1993; Klap et al. 1996), and laboratory bioassays with dark incubation (del Giorgio and Davis 2003; Moran and Covert 2003). Photodegradation studies also track another major pathway of DOM consumption and transformation (1997; Del Vecchio and Blough 2002; Osburn et al. 2009). Spectroscopic techniques such as UV absorption and fluorescence detection [3D excitation-emission matrices (EEMs)] are now used both in source and fate studies (Goldberg 1990; Her et al. 2003; Alberts et al. 2004; Vignudelli et al. 2004; Jaffe et al. 2008).
Two important environmental controls on the quantity and quality of salt marsh outwelling are light availability and extent of inundation (Hemminga et al. 1992, 1993; Kathilankal et al. 2008). The inundation of the salt marsh determines the extent of the surface that may interact and provide DOC to estuarine water, while light availability impacts both in-situ production by autotrophs and transformations through photo-oxidation. Soil decomposition could also change in terms of rates and pathways both because of diminished oxygen availability and because of the flushing of metabolic waste material into the water (Boon 2006). In the global theme of climate change, sea-level rise will increase the areal extent and frequency of inundations, and this could further affect the quantity and quality of organic matter mobilized in a tidal marsh estuary.
Lateral fluxes of organic matter are also an essential component of the short-term salt marsh carbon budget. Several studies have already determined the vertical carbon exchange between marshes and the atmosphere with eddy flux towers (Heinsch et al. 2004; Kathilankal et al. 2008; Guo et al. 2009, 2010; Polsenaere et al. 2012), but they were never coupled to lateral organic and inorganic carbon flux measurements with similar temporal and spatial resolution. Currently, field-ready FDOM fluorometers or UV spectrometers are a potential solution with a fine temporal resolution for in situ measurement of DOC, which represents 90% of primary production released from marshes to estuaries and to the sea (Eldridge and Cifuentes 2000). In addition, since in situ pCO2 and pH probes are available to measure DIC concentrations in tidal waters, it is now possible to close the carbon budget of a salt marsh.
Fluxes of silica
Salt marshes accumulate large amounts of biogenic silicon [BSi, biogenically deposited hydrated amorphous SiO2.nH2O, present in plants, sponges, and diatoms, also referred to as amorphous Si (ASi); Struyf and Conley 2012in sediments and vegetation. This can be recycled to dissolved Si [(DSi), H4SiO4−, the dissolved form of Si available for biogenic uptake, also referred to as silicic acid], mainly in pore water and surface puddles. During ebb tide, this DSi is exported again to the estuary, where it can be an important source of Si for pelagic estuarine diatoms during times of Si limitation.
Where does the build-up of BSi originate from? As discussed in the previous section, marshes receive large amounts of suspended matter during tidal flooding. Together with suspended matter, BSi is imported (e.g., Struyf et al. 2005a). Few studies have actually investigated whether this BSi mainly originates from pelagic diatom production within nearby coastal or estuarine waters or from terrestrial inputs of BSi (e.g., plant Si particles called phytoliths) through rivers discharging into the estuary. This distinction probably depends on the season: in spring and summer, estuarine production of diatoms is high, as reflected in high BSi concentrations in coastal water, coinciding with low DSi due to diatom uptake (e.g., Struyf et al. 2006; Carbonnel et al. 2009). In winter, suspended solids concentrations are often higher within estuaries (e.g., Fettweis et al. 1998; Lesourd et al. 2003), but BSi content of the suspended matter (SPM) is low (Struyf et al. 2007a), which suggests that BSi mainly originates from external terrestrial inputs (e.g., soil run-off), reflected in high concurrent DSi in the estuary (no diatom uptake). In a study in the Scheldt estuary, it was found that absolute import of BSi into marshes is highest in winter, as the higher import of SPM offsets the lower BSi content in the SPM (Struyf et al. 2007a).
Tidal import of BSi is not the only source for BSi accumulation in marshes. A second, very scarcely studied factor is the autochthonous production of diatoms in the marshes. Hackney et al. (2000) indicated that high diatom production in tidal marshes and the food web dependent on this production could actually be important contributors to estuarine production (as earlier suggested by Sullivan and Moncreiff 1990). Macrophytes are another factor in autochthonous production of BSi; aquatic and wetland plants can contain significant amounts of BSi (Schoelynck et al. 2010). In freshwater marshes, Phragmites australis is particularly rich in BSi (Struyf et al. 2007b; up to 5% of the dry biomass in dead reed culms is BSi in saltwater and mesohaline marshes, the dry biomass of Spartina alterniflora and Juncus roemerianus contains up to ±0.5% of BSi (Norris and Hackney 1999; Querné et al. 2012). The relative contribution of autochthonous production vs. tidal import to the total BSi stock in tidal marshes certainly warrants further investigation.
Mass-balance studies show that the magnitude of observed export fluxes of DSi is similar to modeled and experimental results for BSi recycling fluxes (Struyf et al. 2007a, b). There is thus a strong indication that export of Si from the marsh to the estuary is a biologically controlled mechanism, despite large amounts of mineral Si (e.g., clays) that are imported along with suspended matter into the marsh at flood tide. This is because mineral Si is orders of magnitude less soluble than BSi. Finally, the large accumulation of BSi in salt marshes points to a strong role of biology in the Si cycle.
Marshes therefore potentially increase the resilience of coastal waters to dissolved Si limitation and associated phytoplankton shifts to non-diatom communities. N-P-Si ratios are important in controlling estuarine and coastal phytoplankton composition; increased inputs of N and P due to human activities have led to shifts from diatom-dominated communities (which essentially need DSi) to a prevalence of other phytoplankton species (e.g., Smayda 1997) that are less available to higher trophic levels. In comparison to studies on carbon, nitrogen, and phosphorus, results on silicon cycling in tidal marshes are still limited. The general importance of BSi accumulation and DSi delivery by tidal marshes has been confirmed in a growing number of studies (e.g., Struyf et al. 2005a, 2006; Jacobs et al. 2008; Vieillard et al. 2011).
Tidal oscillations systematically flood salt marshes transporting water, sediments, organic matter, and biogeochemical elements such as silica. To measure water fluxes in a salt marsh drained by tidal channels, three different approaches can be adopted, depending on what hydrodynamic quantities need to be computed:
The tidal prism (Equation 1) provides an estimate of the total volume of water exchanged by a marsh in a tidal cycle.
If the value of the instantaneous discharge is needed, the static model of Boon (Equation 2) is simple and adequate.
If we seek the flow velocity or the distribution of residence times, the use of the TIGER model is recommended (Equation 3).
These simplified approaches are particularly suitable for the study of fluxes of biogeochemical compounds in salt marshes and could be easily adopted by researchers working in this area.
Sediment fluxes to and from the marsh strongly depend on sediment resuspension by waves and currents. Recent results show that:
During flood the input of sediment to the marsh depends on resuspension of sediments in adjacent areas by wind waves and tidal currents.
During ebb the export of sediments is strongly affected by the magnitude of water velocity in the channels draining the marsh.
Storm surges import large volumes of sediment to the marsh, but they also export a comparable amount during the subsequent ebb due to the high velocities in the channels and related bottom shear stresses.
Moderate storm conditions with limited surges maximize the sediment import to the marsh.
Knowledge of internal marsh processes and mechanisms affecting both biogenic silicon and organic matter accumulation and turnover is scarce. It is likely that more and more measurement methods will be available in the future to allow us to investigate ecological processes at a finer temporal, spatial, and chemical resolution and at a broader scale.
Regarding lateral flux studies of salt marsh organic matter, the following key topics for future studies are suggested:
Long-term data sets with fine temporal resolution of lateral organic and inorganic matter exchange should be coupled to eddy flux tower data sets to close the carbon budget in salt marshes.
Quality of organic matter should also be measured in tidal fluxes, together with its interactions at different trophic levels.
Linkages between organic matter fluxes and salt marsh physical and physiological processes should be established.
Recent studies on fluxes of organic matter have focused more on the entire estuarine system, including fluxes from the ocean and nearby fluvial watersheds. More research is clearly needed to determine the mechanisms controlling fluxes of organic matter within the marsh system, for example from the marsh platform to the tidal channels and vice versa.
To move knowledge beyond the general pattern of BSi accumulation and DSi delivery, several key topics can be defined:
How does the balance between BSi accumulation and DSi delivery change along gradients of marsh age, salinity, and seasons? Scarce studies so far have indicated net accumulation in tidal freshwater marshes in the Scheldt estuary over a decadal timescale (burial of about 40% of imported BSi without dissolution to DSi). This balance is crucial to understanding the long-term role of tidal marshes in coastal Si cycling: net annual accumulation of BSi could be equally as important as (or even more important than) seasonal delivery of DSi.
What is the importance of Si-rich vegetation and diatom production in tidal marshes for coastal food webs?
What processes potentially impact BSi accumulation and DSi recycling in tidal marshes through their impact on sediment accumulation and vegetation and diatom growth, such as grazing management, sea level rise, invasive species, and hydro-engineering?
SF was supported by NSF award OCE-0924287 and DEB-0621014 (VCR-LTER program).
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.