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Salt marsh hydrology assessment report M. Hensel The role of hydrology and hydrological dynamics in salt marshesis widespread and vital to nearly all marsh processes and restoration efforts. This report will focus on (1) the important aspects of hydrology in the formation and maintenance of salt marshes, (2) types and effects of hydrological disruptions on salt marsh functioning, and (3) the effects of hydrological restoration on a salt marsh and how to evaluate the effectiveness of restoration. Hydrology in salt marsh ecosystems Salt marshes are formed when slow moving water near a protected shoreline, barrier island, or estuary leads to the accumulation of fine sediment which is in turn colonized by halophytic plants (Bertness 1998). In turn, incoming tide water carves channels and builds the intricate salt marsh creek system (Fagherazzi and Kirwan 2012). Once initial plants such as the foundation species Spartina alterniflora are present, marshes grow through self-facilitation by trapping suspended sediments from the water column and creating organic matter (i.e. peat). The formation and regulation of marsh growth is a direct product of the amplitude of the tide and the elevation of the marsh, also known as the hydroperiod (Bertness 1998, Morris et al. 2002, Fagherazzi and Kirwan 2012). Hydroperiod changes locally and regionally but these variations determine the amount of sediment and nutrients that are delivered into marshes via tidewater. In turn, tidal flushing governs fluctuating salinity and oxygen regimes which determines microbial productivity, influence plant zonation, and supports the whole marsh food web (Figure 1) (Magenheimer et al. 1996, Mendelssohn and Morris 1999, Crain et al. 2009). In addition to the hydroperiod, the water table is another important aspect of marsh hydrology that can affect overall marsh processes. The water table in a marsh can vary based on level of tidal flushing, tidal restriction, precipitation, or freshwater runoff (Montalto et al. 2006). Marsh biogeochemistry driven by microbial processes is highly dependent on the water table. If the water table is too low (e.g. drought, tidal restriction), oxygen permeates deep into the peat, increasing rates of decomposition. If the water table is too high (e.g. flooding, outgoing tidal restriction), the waterlogged peat becomes anaerobic, slowing decomposition as organic matter accumulates (Portnoy 1999). As outlined in Figure 1, water table and hydroperiod, as well as water flux, are the important factors that determine hydrology in marshes. Edaphic factors such as salinity, pH, oxygen and sulfide levels are all highly dependent on these hydrological processes. The level of these edaphic factors in turn affects marsh community composition and organization. Marsh biotic structure drives many important ecosystem functions and services such as productivity, decomposition, and nutrient cycling. Like many coastal ecosystems, salt marshes contain a number of biotic feedbacks between these aspects of the model in Figure 1. For example, proper hydrology that supports a healthy plant community in turn will lead to marsh growth through peat accretion, hummock formation, evapotranspiration and decomposition induced marsh platform subsidence. Effects of hydrological disturbance on salt marsh ecosystems Human impacts are widespread drivers of change in marshes throughout the world (Silliman et al. 2009). Besides habitat destruction, restriction or elimination of tidal flow is the largest human disturbance to salt marsh ecosystems, especially in New England (Bertness et al. 2002, Crain et al. 2009). The most common hydrological changes to marshes are from mosquito ditching and the building of dikes, roads, or tidal gates which restrict the amount and frequency of tidal flooding into creeks and onto the marsh platform. Because of the extensive amount of ditching and diking done in New England marshes (i.e. 30% of Maine marshes are tidally restricted and 95% of New England marshes are ditched (Gedan et al. 2009)), researchers have a wide range of examples of the effects of hydrological disturbance on salt marsh processes. Due to the frequency of these hydrological disruptions and the fact that hydrological restoration is the most common type of marsh restoration, most of the effects of the disruption and restoration of tidal flow into marshes should be outlined in the other sections in this report. Below is briefly outlined some of the effects of tidal flow restriction on salt marsh ecosystems Restricting or blocking tidal flow from dikes, tide gates, or culverts, alters the hydroperiod of a marsh, and in turn can negatively affect the soil biogeochemistry, vegetation structure, and animal community (see Figure 1). Some of these impacts, such as the lack of sediment delivery or waterlogged peat, cause decreases in the productivity of the foundation species Spartina alterniflora (Portnoy 1999) and reduce the efficiency of sulfide reducing microbes (Portnoy and Giblin 1997). Also, tidal restriction resulting in desalination of a marsh, often combined with an increase in terrestrial nutrient runoff, can cause a marsh to shift from one dominated by S. alterniflora to dominated by the invasive species Phragmites australis (Silliman and Bertness 2004, Smith et al. 2009). The shift in vegetation from Spartina to Phragmites causes a subsequent crash of the marsh food web (Warren et al. 2002, Silliman and Bertness 2004, Smith et al. 2009) (but see (Burdick and Dionne 1996) which suggests fish may not respond this way). In summary, as figure 1 indicates, changes in marsh hydrology can affect many ecological outputs from local marsh ecosystems. Altered salinity and nutrient delivery, as well as changes in the water table, affect marsh plant communities, which in turn cascades up the whole food web. Evaluating the effects of hydrological restoration in a salt marsh One advantage of the centuries of human impacts on salt marshes is that managers and researchers have a number of case studies on the effectiveness of restoring salt marshes. The first step in a successful project is the actual restoration of tidal flow. Common tidal restorations include either complete flow restoration or an improvement on earlier tidal restriction. Outlined in Warren et al 2002, some of the common restoration events include the removal of tidal gates, installation of self regulating tidal gates, resizing of culverts, outlet/channel dredging or cleaning, and the removal of filled channels (Table 1). Once tidal flow is restored, there are a number of predicted responses from the biological community in the marsh (Table 2). Timing of recovery depends on a number of factors, including length and extent of disturbance, and the type of restoration (Zedler 2000). Specifically, once flow is restored, managers can expect rebounding in the water table, salinity of the marsh platform, and subsequent change in marsh vegetation (i.e. return to Spartina from Phragmites) (Burdick and Dionne 1996). As the plant community returns to its natural state, invertebrate, fish, and bird communities will rebound (Warren et al. 2002, Gedan et al. 2009), but the timing of these events varies from marsh to marsh (Roman et al. 1995, Burdick and Dionne 1996). The relationship between time since initial disturbance and expected rate of recovery after restoration is currently unknown, but this may vary predictably with degree of hydrological restoration and the state of the prerestored marsh. To evaluate the effectiveness of marsh restoration, researchers and managers need to implement a number of monitoring protocols to understand how hydrology and the marsh community respond to tidal flow restoration. Neckles et al 2012 outline a number of ways to measure the success of marsh restoration loosely related to the functions and services desired by managers. First, to understand how hydrological restoration has affected the way that tides flood the marsh, it is important to monitor tidal heights and the elevation of the marsh relative to tidal heights. Although tidal buoys and reports are often accurate, the exact amount of marsh platform flooding can only be determined by direct, local measurements such as a contour map. Measuring the tidal signal and elevation should be done over at least a month to see how flooding changes across multiple moon phases. Some of the best methods for this monitoring are through the use of continuous water level recorders. Also, to further evaluate the effectiveness of restoration on hydrological dynamics, managers should monitor the changes in tidal creeks thought permanent cross section profiles of said creeks. Water table depth should also be measured through permanent groundwater wells installed within the marsh and can be used to determine if the water table is responding to restoration. Finally, water quality parameters in the main channel and within porewater should be monitored to determine if changes in dissolved oxygen, salinity, temperature, and pH have corresponded with the restoration efforts. An important aspect of marsh restoration that is often ignored is the changes in marsh functioning and services before and after restoration takes place. A pre-restoration marsh, despite often dominated by the highly productive and deep rooting Phragmites, still provides a number of ecosystem services that are important to humans. Because of its high growth rate, Phragmites most likely is an important carbon sequesterer and shoreline protector. In fact, some marsh restorations in highly nutrient rich areas (e.g. around a coastal airport) may seek out Phragmites as opposed to Spartina marshes. Based on this, managers and researchers should try to quantify changes in ecosystem functions and services throughout the restoration process. As mentioned in this report, plant and animal communities are different in restored and disturbed marshes, but how service provision changes with time since restoration is unknown. One would expect that, as a restoration progressed, some services might be lost or reduced (e.g. runoff filtration, shoreline protection) while others are increased (e.g. aesthetic value of marshfront property, recreation from bird watching). As well as implementing the monitoring protocols outlined in the first part of this section, managers should closely measure functions and services before, during, and after marsh hydrological restoration efforts. HYDROLOGY Tidal inundation Water Table level Water flux Biotic feedbacks Peat accretion Hummock formation Evapotranspiration Decomposition-induced subsidence EDAPHIC FACTORS Oxygen/ Sulfides Salinity pH Biotic Feedbacks Shading Evapotranspiration Oxygenation of rhizosphere BIOTIC STRUCTURE Species Composition Zonation Biotic Feedbacks Species interactions ECOSYSTEM PROCESSES Nutrient cycling Productivity Diversity Decomposition Figure 1 from Crain et al. 2009). Edaphic factors in a marsh are driven by hydrological processes such as tidal inundation and water table. These factors in turn affect the biotic structure of the marsh which has important feedbacks with the overall marsh ecosystem and hydrology. Important marsh ecosystem processes that drive marsh services are the output of this model, indicating that all of these processes are tightly connected Table 1, from Warren et al 2002. Six of the most common marsh restoration approaches used in Connecticut over the last 45 years. Note that rarely is tidal flow completely restored, as tide-gate removal and culvert resizing are the most common restoration techniques. Table 2 from Burdict et al 1997. Summary of responses in salt marsh functions to tidal restriction and restoration in a Maine andba New Hampshire marsh. In these examples, marsh elevation, water table, salinity, plant cover and community composition responded positively to marsh restoration. Here, fish consumers did not have a significant increase in abundance in response to restoration (Figure 9 in Burdict et al 1997) Literature cited Bertness, M. 1998. The Ecology of Atlantic Shorelines. Sinauer Associates Inc. Bertness, M. D., P. J. Ewanchuk, and B. R. Silliman. 2002. Anthropogenic modification of New England salt marsh landscapes. Proceedings of the National Academy of Sciences of the United States of America 99:1395–8. Burdick, D., and M. Dionne. 1996. Ecological responses to tidal restorations of two northern New England salt marshes. Wetlands Ecology and … 4. Crain, C. M., K. Bromberg-Gedan, and M. Dionne. 2009. Tidal restrictions and mosquito ditching in New England marshes: Case studies of the biotic evidence, physical extent and potential for restoration of altered tidal hydrology. in B. R. Silliman, M. D. Bertness, and T. Grosholz, editors. Human Impacts in Salt Marshes: A Global Perspective. University of California Press. Fagherazzi, S., and M. Kirwan. 2012. Numerical models of salt marsh evolution: ecological, geomorphic, and climatic factors. Reviews of …:1–28. Gedan, K. B., B. R. Silliman, and M. D. Bertness. 2009. Centuries of human-driven change in salt marsh ecosystems. Annual review of marine science 1:117–41. Magenheimer, J., T. Moore, G. Chmura, and R. Daoust. 1996. Methane and carbon dioxide flux from a macrotidal salt marsh, Bay of Fundy, New Brunswick. Estuaries 19:139–145. Mendelssohn, I., and J. Morris. 1999. Ecophysiological controls on the productivity of Spartina alterniflora. Pages 59–80 in M. Weinstein and D. Kreeger, editors. Concepts and Controversies in Tidal Marsh Ecology. Kluwer Academic Publishers, Boston. Montalto, F. a., T. S. Steenhuis, and J.-Y. Parlange. 2006. The hydrology of Piermont Marsh, a reference for tidal marsh restoration in the Hudson river estuary, New York. Journal of Hydrology 316:108–128. Morris, J., P. V. Sundareshwar, C. T. Nietch, B. Kjerfve, and D. R. Cahoon. 2002. Responses of Coastal Wetlands to Rising Sea Level. Ecology 83:2869–2877. Portnoy, J., and A. Giblin. 1997. Effects of historic tidal restrictions on salt marsh sediment chemistry. Biogeochemistry:275–303. Portnoy, J. W. 1999. Salt Marsh Diking and Restoration: Biogeochemical Implications of Altered Wetland Hydrology. Environmental Management 24:111–120. Roman, C. T., R. W. Garvine, and J. W. Portnoy. 1995. Hydrologic modeling as a predictive basis for ecological restoration of salt marshes. Environmental Management 19:559–566. Silliman, B., and M. Bertness. 2004. 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