Impact of Barrier Breaching on Wetland Ecosystems under the Influence of Storm Surge, Sea-Level Rise and Freshwater Discharge
Coastal wetland ecosystems and biodiversity are susceptible to changes in salinity brought about by the local effects of climate change, meteorological extremes, coastal evolution and human intervention. This study investigates changes in the salinity of surface water and the associated impacts on back-barrier wetlands as a result of breaching of a barrier beach and under the compound action of different surge heights, accelerated sea-level rise (SLR), river discharge and rainfall. We show that barrier breaching can have significant effects in terms of vegetation die-back even without the occurrence of large storm surges or in the absence of SLR, and that rainfall alone is unlikely to be sufficient to mitigate increased salinity due to direct tidal flushing. Results demonstrate that an increase in sea level corresponding to the RCP8.5 scenario for year 2100 causes a greater impact in terms of reedbed loss than storm surges up to 2 m with no SLR. In mitigation of the consequent changes in wetland ecology, regulation of relatively small and continuous river discharge can be regarded as a strategy for the management of coastal back-barrier wetland habitats and for the maintenance of brackish ecosystems. As such, this study provides a tool for scoping the potential impacts of storms, climate change and alternative management strategies on existing wetland habitats and species.
KeywordsWetland ecosystem Barrier breach Climate change Accelerated sea level rise Storm surge Freshwater discharge Wetland loss Reedbeds Mitigation strategies Coastal wetland management strategies
Wetlands are commonly found along low energy coastal environments, and provide important ecosystem services and economic benefits (e.g., Gedan et al. 2009, 2011; Ndebele and Forgie 2017; Li et al. 2018). The resilience of these coastal ecosystems under a changing climate is uncertain, as they are under pressure from accelerated sea-level rise (SLR) and changes in the frequency and/or magnitude of storms (e.g. Leonardi and Fagherazzi 2014; Chambers et al. 2016; Leonardi et al. 2017). Indeed, a recent study shows a high probability for salt marsh retreat under projected future sea-level rise (Horton et al. 2018), whilst Leonardi et al. (2017) stresses the critical importance of storms in determining the long-term response. Depending on the region, and various environmental factors, predicted wetland loss by the end of the century has been estimated to be around 0 to 50% (Gilman et al. 2006; McFadden et al. 2007; Alongi 2008; Kirwan et al. 2016). This is likely to be an underestimate given that sea-level rise over this century could double previous projections (Grinsted et al. 2015; Bamber et al. 2019). Further, financial resource limitations may require a move from ‘hold the line’ to ‘no active intervention’ or ‘managed realignment’ options (Esteves and Williams 2017) for coastal management which can potentially impact back-barrier wetlands and habitats (Rupp-Armstrong and Nicholls 2007; Friess et al. 2014; Brady and Boda 2017). Notable managed realignment examples in the UK include Tollesbury (Garbutt et al. 2006), Freiston (Friess et al. 2014), Hesketh Marsh (Tovey et al. 2009), and Medmerry (Dale et al. 2017, 2018).
Coastal wetlands can be significantly affected by increases in water levels through the following three major ways: increased inundation period, increased surface erosion and salt-water intrusion (Blankespoor et al. 2014). Although increased flooding can potentially aid the survival of wetlands through promoting sedimentation and biomass growth (e.g. Kirwan et al. 2016; Schieder et al. 2018), changes in the extent and duration of marine inundation can cause die-back of the less salt tolerant species, and landward migration of vegetation types that are more resilient to increased hydroperiod (Donnelly and Bertness 2001). Changes in high water levels as a consequence of storm surges or SLR are thus linked to potential changes in biodiversity (e.g. Field et al. 2016; Kirwan et al. 2016). Indeed, increased salinity due to higher sea levels has been causing land degradation in many coastal areas worldwide, compromising food production and freshwater availability (e.g. Milliman et al. 1989; Craft et al. 2009; Lovelock et al. 2015). In the UK, for instance, land degradation as a consequence of storm surges is becoming a pressing issue. The Environment Agency has estimated that 432,000 ha of agricultural land with a capital value of over £132 billion are potentially at risk from surge-driven coastal flooding (Halcrow Group Ltd et al. 2001).
Unlike SLR, which is a gradual and long-lasting change in water levels, storm events are more unpredictable and short-lived, and changes caused by storm events can be more dramatic in the short term due to their high-energy nature (e.g. Gable et al. 1990; Walker 1991; Orr and Ogden 1992; Duever et al. 1994). Apart from damage associated with physical stresses (e.g. uprooting), storms can increase the salinity of inland water, hence causing changes in physicochemical properties of wetland soil; the combination of which will then alter the metabolic functions responsible for plant productivity (DeLaune et al. 1987; Michener et al. 1997; McKee et al. 2016).
By regulating their respiration rate, plants are generally able to adjust themselves to soil conditions, or influence soil conditions in their favour (Sternberg et al. 2007). For instance, plants that have low salinity tolerance can down-regulate evapotranspiration during dry season to maintain low soil salinity. Therefore, a small disturbance that changes the soil conditions by just a small amount can be offset through adaptation by the local vegetation. For a disturbance to cause vegetation die-back or a regime shift, the event has to cause changes in environmental conditions that exceed certain threshold criteria in terms of strength and/or duration of the impact on the system (Jiang et al. 2014). When the severity of the event, e.g. surge height or duration of flooding, is such that threshold criteria are exceeded, a shift in nature, size and distribution of plant communities across coastal wetlands is likely to occur (DeLaune et al. 1987; Teh et al. 2008; Chambers et al. 2016).
Storm events can also cause morphological changes along the coastline which can potentially further exacerbate stressors connected to increased salinity. For instance, processes such as chronic coastal erosion, the breaching of sand dunes and barrier beaches due to over-wash, or the degradation of coastal protection structures will cause a landward migration of the flood limit, enhancing the risk for inland ecosystems. This is especially important for those cases where management strategies follow the ‘no active intervention’ approach, and for which newly-formed breaching or erosion are a long-lasting condition (Rangel-Buitrago et al. 2018). Indeed, this is also relevant to sites where managed realignment is a likely future option for coastal management, and where the re-establishment of perimarine wetlands has the potential to contribute to sustainable and diverse coastal economies (Plater and Kirby 2006).
This research models potential changes in the salinity of surface water in the back-barrier, brackish wetlands of RSPB Minsmere Nature Reserve (see Study Area), as a case study, in response to combinations of SLR, coastal storms and freshwater inflow following breaching of the barrier beach. Here, we focus on the salinity of the standing water ‘post-breach’, as determined by tidal rise and fall through the breach, tributary river discharge and local rainfall but excluding the influence of groundwater input and seawater seepage through the coastal barrier. Attention is given to the exceedance of threshold salinity criteria necessary for local vegetation die-back.
At Minsmere, the present sea defences include a line of natural and modified sand dunes and sand and gravel ridges spanning the coastline (Fig. 1). The dunes and barrier beach, which are formed of sands and gravels transported alongshore from erosion of the Pliocene and Pleistocene cliffs further north (Brooks et al. 2012), overlie a sequence of unconsolidated Holocene and early Pleistocene sediments that extend beneath the Minsmere wetland (Hamilton et al. 2019). The general character of the coastline has been one of southward sediment transport alongside landward recession due to post-glacial sea-level rise, although recent work has shown little evidence of regionally coherent forcing at either centennial (post-1880s) or intra-decadal (post-1990s) timescales (Burningham and French 2017). Prior to the early Middle Ages, the study area was an open estuary formed as a result of early to mid-Holocene flooding of low level river valleys but was cut off from the sea and enclosed by a coastal barrier in the eighteenth century (Pye and Blott 2006). A secondary clay embankment also runs along the back of the dunes in the northern part of the study site (EA 2009; Prime et al. 2015). According to the UK Environment Agency (EA), the long-term stability of these defences is significantly threated by coastal erosion processes, particularly to the north of the RSPB Reserve. For instance, the northern end of the defences was breached due to tidal surges in November 2006 and 2007, leading to flooding of the area between the dunes and the secondary clay embankment (EA 2009). Hence, a cross bank (Coney Hill Cross Bank in Fig. 1) was built to isolate the northern part of the site from any flooding from the sea. Within the wetland area, a complex network of ditches has been created and maintained to manage water levels through controlled drainage by a manual sluice located midway along the coast (Fig. 1). However, given the projected SLR and costs associated with the maintenance of the sluice and the barrier beach, sustained management of freshwater habitats in Minsmere is not a sustainable long-term option (Pye and Blott 2006). Indeed, the Shoreline Management Plan priorities for the 20, 50 and 100 years epochs are currently identified as ‘managed realignment’, with the exception of the short section of barrier beach are the north of the site which has a ‘no active intervention’ policy in place for the 100 year epoch (see Sizewell case study at: https://arcoes-dst.liverpool.ac.uk/).
Managed realignment of the Minsmere shoreline will have significant impacts on the freshwater reedbed environments that currently characterize much of this back-barrier wetland. Research has previously established the tolerance of P. australis to salinity (e.g. Ranwell 1964; Roman et al. 1984; Matoh et al. 1988; Robbins et al. 1991; Hellings and Gallagher 1992). It has been found that the tolerance varies depending on the location and growth stage of the plant. For example, while adult plants of the high salinity tolerant US clone can survive at salinities near 65 psu, the juvenile plants may die at 35 psu (Engloner 2009). On the other hand, the salt tolerance of P. australis in Europe has been found to vary between 5 and 25 psu. In the current investigation, following Lissner and Schierup (1997) and Hellings and Gallagher (1992), we assume a die-back of P. australis when salinity is above 22.5 psu for a continuous period of 42 days. Consequently, this modelling approach for scoping the potential impacts of barrier breaching on reedbed habitats, whether an intended consequence of management or an unintended result of climate change and/or storms, provides important information for shaping present actions and future decisions regarding the site.
With a single breach located in the barrier beach, the study area takes the form of an estuary that features shallow water depth and two-dimensional horizontal circulation and mixing (e.g. hydrodynamic class E estuary in Hume et al. 2007). Here, the shallow water depth enhances the importance of wind-driven mixing, hence limiting the development of stratification through the water column. The two-dimensional (2DH) mode of the numerical model Delft3D (Delft Hydraulics 2014) was therefore used to compute the hydrodynamics and salinity of the Minsmere wetlands. The calculation of salinity is based on the classic advection-diffusion equation (Delft Hydraulics 2014). The computational domain and terrain height with respect to mean sea level for the study area are presented in Fig. 1. The terrain height of the model is obtained from the combination of two datasets: bathymetric data downloaded from EDINA DIGIMAP for the open sea and LiDAR data (DTM Composite England 2 m; tile references are given in the supplementary material) provided by the Environment Agency for the wetland regions. Vertical Offshore Reference Frame (VORF) corrections provided by the UK Hydrographic Office have been applied to adjust these two datasets to Mean Sea Level (MSL). Resolution of the model grid varies from 30 m in the nearshore to 10 m in the wetland. The model has two open boundaries: the east boundary (OB1 in Fig. 1) is placed ~ 1.2 km offshore in the open sea and the west boundary (OB2 in Fig. 1) is located ~ 4.0 km inland. The east boundary is driven by data extracted from a calibrated larger scale model (Leonardi and Plater 2017) covering the coastline of South East England (see larger model domain denoted in Fig. 1 inset). Validation of the model described herein, however, is not carried out due to lack of available data.
An input of freshwater discharge ranging from 3 to 9 m3/s has been prescribed for the main drainage channel, the New Cut, which terminates at the sluice through OB2. Model runs have been carried out for idealized test cases with the sluice being breached (either naturally or artificially), i.e. the height of the ridge at the sluice has been lowered to match that of the surrounding areas. The width of the breach has been set equal to the width of the sluice. In this case, the breach morphology is neither created nor evolved by the storm surge. The breach has been located at the sluice as it is the focal point of the drainage network and a breach at this location is expected to maximize the landward intrusion of marine water and, thus, represents the worst case scenarios in terms of the areal extent of the zone affected by increased salinity.
Spatial Distribution of Surface Water Salinity
Opposite to the overall increase in salinity over time beyond the storm event observed in the cases without river discharge (Fig. 3), surface water salinity across the wetland of the 3 and 9 m3/s discharge scenarios decreases once the surge comes to an end: a freshwater wedge is observable north to the New Cut in all scenarios 42 days after the end of the surge. For the rainfall cases (Fig. 6), although the more limited landward intrusion of the salinity front is also observed at the end of the surge, freshwater wedges are not formed after 42 days post-storm. Instead, more widely distributed salinity contours are formed, and the contours are similar to each other.
To scope the temporal trends of salinity in the back-barrier wetland under the above-mentioned scenarios, surface water salinity is sampled at eight locations, four along the New Cut and four on the two sides of the New Cut (Fig. 1), for the duration of the simulation. Figures showing time series of salinity of the above-mentioned cases at the eight locations, as well as the associated discussion, are given in the supplementary material.
Salinity over Distance at the End of the Beach Event
Effects of surge height, SLR, freshwater discharge and rainfall on salinity over distance at the end of the breach event
Freshwater discharge (m3/s)
Increases from 0 to 9
• The rate of salinity decrease over distance is not sensitive to surge height/SLR;
• Freshwater recovery rate over distance increases when discharge increases;
Surge increases from 1 to 3
• Salinity is overall higher when the storm surge is higher;
• Freshwater recovery rate of the system over distance decreases with increasing storm height;
Comparison between surge and SLR
• SLR has the largest surface water salinities when discharge is 0;
• Surface water salinities of the SLR cases are lower than those of the 2 m surge cases, but larger than those of the 1 m surge cases, when discharge is 3 and 9;
• Surface water salinities of the SLR case are at the same level of those of the 2 m surge case.
For the 0 m3/s discharge cases, most of the wetland is recognized as potential die-back area. Areas north to the Coney Hill cross bank only meet the criterion when a 3 m surge is imposed. The potential die-back area is significantly reduced for the 3 m3/s and 9 m3/s discharge cases. In particular, wedge-shaped die-back-free zones stretching to the barrier breach are formed north of the New Cut for the 0–2 m surge scenarios with 3 m3/s discharge, and the potential die-back area north to the New Cut becomes almost negligible for the same scenarios with 9 m3/s discharge. For both discharges, the area north to the Coney Hill cross bank turns into potential die-back zone only when the surge height is 3 m. For the rainfall cases, the distribution of the potential die-back area is less affected by surge occurrence. In comparison with the freshwater discharge cases, although the potential die-back areas in the main floodplain of the rainfall cases are larger, areas north of the Coney Hill cross bank and southern areas are always die-back-free zones, even when surge height reaches 3 m.
SLR of 0.9 m is observed to increase the reedbed loss of all four cases. Freshwater discharge through the main channel of the ditch network within the wetland can effectively reduce the SLR-induced reedbed loss. In particular, a discharge of 9 m3/s can reduce the reedbed loss from 74 ha to 5 ha. On the other hand, very little effect of rainfall on reedbed loss is observed. Compared to the impact of storm surges, reedbed loss due to SLR is equal to the damage caused by a 2 m surge, given no freshwater is being input into the wetland. For the 3 m3/s discharge cases, the reedbed loss caused by SLR is slightly larger than that caused by the 3 m storm surge; the losses are 58 ha and 54 ha, respectively. The SLR-caused reedbed loss with the 9 m3/s discharge case lies between the damage caused by the 2 m and 3 m surges with the same rate of freshwater input. When rainfall is the source of freshwater input of the system, SLR causes a significantly larger destruction to the reedbed of the wetland than storm surges. While the reedbed losses caused by the storms remain at a level of 50–60 ha, the loss is increased to 74 ha for the SLR case.
This research explores reedbed die-back in a coastal back-barrier wetland following a barrier breaching event. The modelled salinization of wetland areas due to sea/freshwater exchange, storm events and SLR has been identified as a major threat for reedbeds, and a threshold criterion is here used to determine the survival/die-back of reedbeds under different external forcing scenarios. As such, the modelling can be viewed as a tool for scoping the impact of different flooding phenomena or the consequences of alternative management strategies on wetland habitats and biodiversity. Although not exhaustive, the value of this approach lies in exploring the vulnerability of coastal wetlands to climate and coastal change under ‘no active intervention’ shoreline management, from event to centennial timescales (Cowell and Thom 1994), and in shaping strategies and interventions for effective ‘managed realignment’. Here, we examine the modelling results in relation to how they may feed into decision support for coastal wetland management and climate change adaptation.
Our results show that without any mitigation plan in place, such as regulated freshwater inputs, the majority of the current reedbeds in Minsmere will be lost due to increased salinity in case of breaching of the coastal defences. For example, even under calm conditions (0 m surge) and without SLR, water exchange caused by the breaching alone can lead to a 44% loss of the current reedbeds extent, and the reedbed loss under calm conditions but with 0.9 m SLR can increase to ~ 78% (Fig. 11). In this respect, the reedbed habitat currently exhibits considerable vulnerability to event-based barrier breaching during periods of low freshwater discharge, which increases substantially with SLR. This implies a requirement for both immediate and long-term mitigation, likely in the form of ‘compensatory habitat’ creation, which is already in plan for the Ouse and Nene Washes (Natural England. 2016).
Tests incorporating freshwater input in the form of direct river discharge were run to address saline intrusion compared with cases with rainfall. Compared to rainfall, which provides an evenly distributed freshwater input for the area, the impact of river discharge is more spatially-focused, and the spatially-limited distribution of freshwater is further constrained by the topography. Therefore, the chances of reedbed survival are only increased for areas that are closer to the freshwater passage. However, despite the small discharge values, discharge inputs are more efficient than rainfall in offsetting the salinity increase, and hence for the test case herein deliver more effective mitigation in reducing total reedbed die-back for surge values up to 3 m and for SLR up to 0.9 m. In the immediate term, i.e. wetland resilience to breaching under ‘no active intervention' scenario, the reedbeds are located where freshwater passage is good and, hence, if breaching took place during winter or periods of high river discharge (as is often associated with storms), the reedbed loss would be moderated substantially. Presently, it is rare that freshwater discharge into Minsmere reaches the modelled high scenario to achieve complete resilience to tidal ingress, and if breaching took place during summer the effects on reedbed extent would be far reaching. In the long-term, aside from the costs of implementing a water storage and management scheme for mitigation by river discharge input, additional challenges come from climate change and increased domestic and agricultural water demand in the south and east of England (Defra 2013). In relation to climate change, the UK Climate Projections 2018 (UKCP18) projected that average summer rainfall in the UK could decrease by up to 47% while average winter rainfall could increase by up to 35% by 2070. Such a future would necessitate an effective water storage and management scheme to maintain reedbed resilience during the summer months. Overall, the model results suggest that continuous and targeted freshwater discharge could be regarded as a potential mitigation strategy under both ‘no active intervention’ and ‘managed realignment’ scenarios but only if sufficient freshwater resources are available and can be managed appropriately. This would seem less likely for a ‘managed realignment’ future, and thus the inland habitat compensation option, described above, is a more viable option.
Comparison between the impacts of storm surges and SLR has been carried out. Our results show that in terms of hectare loss of reedbeds, a 0.9 m SLR has a greater impact than surges up to 2 m height with no SLR, especially for cases where wetland loss mitigation measures are being implemented with 3 and 9 m3/s discharge regulation. This is due to the fact that for the SLR scenarios the baseline sea level is continuously higher throughout the entire simulated period, which facilitates the ingress of seawater into the wetland, hence the increase of salinity of the surface water. Further, compared to the temporary nature of the water level increase caused by storm surges, the raising of baseline mean sea level caused by SLR is an event with a much longer duration which can lead to long-lasting flooding of the wetland, causing greater damage to the vegetation of coastal wetlands through prolonged submergence of the plants and salinization of the water system. In terms of decision support, this implies that the current mosaic of habitats in Minsmere wetlands is unlikely to be sustained into management epoch 2 (20–50 years), and that another wetland complex will be required for epoch 3 (50–100 years) – one that is much more aligned with a tidally flushed barrier estuary (Roy et al. 1994), characterised by tidal creeks, mudflats, saltmarshes and marginal reed swamps. Whilst this would represent a significant change in the natural resource base, it would essentially be a return to the ‘Haven’ that existed on site prior to its closure in the eighteenth century (Pye and Blott 2006).
As a nature reserve, the study site serves as a good representative of coastal habitats that are homes to a wide range of plants and animals. Therefore, in addition to the die-back of reeds, increased salinity in the wetland would also pose pressure on the survival of other species. Our results show that the current reedbed extent is likely to shrink over the long term under the threat of increased salinity in the wetland, which agrees with previous finding suggesting that the expansion of P. australis is limited by high salinities (Chambers et al. 1999). However, the salinization of the wetland does not necessarily mean a complete eradication of the existing habitat and the reliant communities which are adaptive to the changing environment. The intrusion of saline water could present opportunities for reedbed colonization on the landward side of the domain, hence the relocation of animals that are dependent on reedbed. Indeed, colonization and expansion of P. australis on the high marsh areas under certain conditions have been widely reported in the US (Chambers et al. 1999; Bart and Hartman 2000; Bertness et al. 2002). However, apart from hydrodynamic factors, nutrient regime also plays an important role in determining the early establishment and growth of reedbeds (Chambers et al. 1999). In this respect, habitat compensation due to wetland development elsewhere represents a more reliable strategy associated with ‘managed realignment’ of Minsmere.
In addition to the above-mentioned potential migration of the reedbed and its reliant ecological communities on the high marsh, an increased surface water salinity in the wetland could also facilitate the establishment of plants with higher salt-tolerance in the low marsh (Donnelly and Bertness 2001), and thus lead to a habitat shift. For example, competitive interactions may exist between P. australis and S. alterniflora at moderate salinities, but S. alterniflora is more likely to survive and replace P. australis at high salinities due to specialised glands on the leaves which allow efficient osmoregulation and salt excretion (Howes et al. 1986; Vasquez et al. 2006; Medeiros et al. 2013). Therefore, controlled introduction of highly salt-tolerant plants and their dependent communities in low marsh areas could potentially serve as a solution to retain bio-diversity posterior to the salinization of back-barrier brackish wetlands.
The results presented in this research are based on one idealized breach location, i.e. the manually controlled sluice of the drainage system in the wetland; this idealized scenario was chosen as it maximizes the seawater ingress into the system through transmission within the existing drainage network. In which case, it might be regarded as a ‘worst case’ for seawater ingress, increased salinity and reedbed die back. However, breaching can happen at different locations, which then leads to the question of how critical the breach location is in terms of inundation extent, water salinization and ecosystem destruction. For instance, had the breach happened north of Coney Hill cross bank, the main wetland area would likely be protected by this secondary defence from the impacts of both storm surges and SLR. Also, the damage caused to the wetland is likely to be reduced if the breach is situated further south of its current location, as the area south of the New Cut is higher elevation with fewer drainage channels and weaker channel connectivity, hence reduced water exchange and salinity diffusion. When the breach is located between the sluice and the cross bank, sea water ingress would be slower if the seawater being flushed into the wetland remains confined within the drainage channels, relying on the channel network to progress. However, if the amount of seawater input is large enough to overflow the channel banks and bypass the channel network to diffuse across the wetland, the efficiency of sea water ingress is then independent of the location of the breach.
In considering the implications of seawater ingress for both the ‘no active intervention’ and ‘managed realignment’ futures, wetland response need not have to develop naturally following breaching. Direct interventions in the back-barrier to steer landscape evolution in the wetland, such as creating creeks and developing the necessary topography, can ultimately compensate for habitat loss induced by seawater intrusion (e.g. Dale et al. 2017, 2018; Lawrence et al. 2018). For example, the fast seawater ingress promoted by high connectivity of the drainage network mentioned above could be impeded by construction of embankments that disconnect the network. In a like manner, channels could be created by design to route seawater away from the reedbeds if the goal was to retain the reedbeds at their current establishment.
A numerical model (Delft3D) is used in this research as a tool to study the impact of barrier breaching on a back-barrier wetland located on a micro-mesotidal coast. The methodology applied in this research to investigate responses of wetland vegetation to environmental stressors, i.e. combining key environmental factors predicted by state-of-the-art numerical models and the tolerance of plants to these factors, is readily transferable to studies with a similar research focus and, indeed, to sites where ‘managed realigment’ is an agreed option for coastal resource management over the longer term. Similarly, the outcomes of this research illustrate the potential impacts of environmental changes on vegetation in micro-mesotidal back-barrier wetlands, e.g. Donaña National Park in southern Spain and Elkhorn Slough National Estuarine Research Reserve in California. Tidal environments characterized by low tidal range have been found to experience restricted water exchange between the enclosed coastal wetlands and coastal waters (Childers and Day Jr 1988; Ibñez et al. 2002; Sánchez-Carrillo et al. 2009), which also suggests a limited exchange of salt between the two water bodies. It can, therefore, be deduced that meso- and macrotidal environments which typically have larger tidal prism are likely to undergo greater water and salt exchange and, hence, experience more severe breaching-induced surface water salinization.
This research explores the potential state of a coastal wetland with a barrier breach either due to coastal erosion consequent upon accelerated sea-level rise, instantaneous breaching during a storm, or as a result of human intervention. Predicted extensive vegetation die-back due to prolonged highly saline conditions caused by sea/freshwater exchange through the breach revealed the vulnerability of coastal back-barrier wetland. Analyses were conducted under the compound action of SLR, freshwater inputs and different storm surge scenarios. The comparison between storm surges and SLR-induced impacts in terms of hectares loss in reedbeds revealed that a 0.9 m SLR (RCP 8.5 projection for year 2100) had a greater impact than a surge up to 2 m height with no SLR, either with or without regulative freshwater input. The potential of utilizing continuous and targeted freshwater discharge to mitigate SLR and/or surge-induced disruption on wetland salinity to guarantee habitat stability has been investigated. We found that constant freshwater discharge can largely reduce areas affected by salinity increments and areas possibly subject to reedbed die-back. This is, of course, dependent on the availability of sufficient stream discharge to meet the required regulatory demand.
The numerical model used in this research provides a useful tool for scoping the impact of barrier breaching on back-barrier wetlands under both ‘no active intervention’ and 'managed realignment’ options for coastal resource management. Due to the wide extent of coastal wetlands, and their importance in supporting bio-diversity and providing coastal protection, the findings of this research are highly important to the planning and management of coastal wetlands. This can be reflected in the identification of vulnerable locations, projected areal changes in wetland composition and distribution, and the evaluation of potential mitigation strategies according to the time frame being considered. The model therefore offers an important tool for exploring the potential consequences of alternative management strategies under different environmental forcings.
This work was supported by the NERC research grant: NE/N015614/1, Physical and biological dynamic coastal processes and their role in coastal recovery (BLUE-coast), and the N8-AgriFood award, NCG10111, Toward an integrated approach for salt intrusion and salinization management in soil and aquifers for sustainable agriculture.
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