The Effects of Road Culverts on Nekton in New England Salt Marshes: Implications for Tidal Restoration

In recent years, salt marsh restoration projects have focused upon restoring hydrology through culvert enlargement to return functional values lost due to reduced tidal flow. To evaluate culvert effects on upstream nekton assemblages, fyke nets were set upstream of tidally restricted creeks, creeks recently restored with larger culverts, and paired reference creeks in New Hampshire and Maine, U.S.A. Subtidal habitats created or enlarged by scour were found immediately upstream of undersized culverts. All marshes supported similar assemblages and densities of fish, suggesting that marshes upstream of moderately restrictive culverts provide suitable habitat to support fish communities. However, densities of Crangon septemspinosa (sand shrimp) were significantly reduced upstream of culverts. A mark–recapture study was conducted in tidally restricted, restored, and reference marsh creeks to evaluate culvert effects on the movement of Fundulus heteroclitus (mummichog), the numerically dominant fish species in New England salt marshes. Recapture data indicated that small culvert size and consequently increased water velocity significantly decreased fish passage rates. We infer that upstream subtidal habitats and greater water velocities due to undersized culverts decreased nekton movements between upstream and downstream areas, resulting in segregated nekton populations. Restoration of salt marsh hydrology by the installation of adequately sized culverts will support increased fish access to marsh habitats and nekton‐mediated export of marsh‐derived production to coastal waters.     

Modeling Habitat Change in Salt Marshes After Tidal Restoration

Salt marshes continue to degrade in the United States due to indirect human impacts arising from tidal restrictions. Roads or berms with inadequate provision for tidal flow hinder ecosystem functions and interfere with self‐maintenance of habitat, because interactions among vegetation, soil, and hydrology within tidally restricted marshes prevent them from responding to sea level rise. Prediction of the tidal range that is expected after restoration relative to the current geomorphology is crucial for successful restoration of salt marsh habitat. Both insufficient (due to restriction) and excessive (due to subsidence and sea level rise) tidal flooding can lead to loss of salt marshes. We developed and applied the Marsh Response to Hydrological Modifications model as a predictive tool to forecast the success of management scenarios for restoring full tides to previously restricted areas. We present an overview of a computer simulation tool that evaluates potential culvert installations with output of expected tidal ranges, water discharges, and flood potentials. For three New England tidal marshes we show species distributions of plants for tidally restricted and nonrestricted areas. Elevation ranges of species are used for short‐term (<5 years) predictions of changes to salt marsh habitat after tidal restoration. In addition, elevation changes of the marsh substrate measured at these sites are extrapolated to predict long‐term (>5 years) changes in marsh geomorphology under restored tidal regimes. The resultant tidal regime should be designed to provide habitat requirements for salt marsh plants. At sites with substantial elevation losses a balance must be struck that stimulates elevation increases by improving sediment fluxes into marshes while establishing flooding regimes appropriate to sustain the desired plants.     

Early Responses of Fishes and Crustaceans to Restoration of a Tidally Restricted New England Salt Marsh

Nekton (fishes and decapod crustaceans) is an abundant and productive faunal component of salt marshes, yet nekton responses to tidal manipulations of New England salt marshes remain unclear. This study examined nekton use of a tidally restricted salt marsh in Narragansett, Rhode Island relative to an unrestricted marsh during summer. In addition, a before‐after‐control‐impact design was used to examine early responses of nekton to the reintroduction of natural tidal flushing. Species richness and densities of Cyprinodon variegatus, Lucania parva, Menidia beryllina, and Palaemonetes pugio were higher in the restricted marsh compared with the unrestricted marsh. The unrestricted marsh supported higher densities of Menidia menidia and Fundulus majalis. Mean lengths of Carcinus maenas and P. pugio were greater in the restricted marsh. Tidal restoration resulted in increased tidal flushing, salinity, and water depth in the restricted marsh. Densities of Fundulus heteroclitus, F. majalis, and Callinectes sapidus were higher after 2 years of restoration. Density of L. parva decreased after restoration, probably in response to a loss of macroalgal habitat. Species richness also decreased after 2 years, from 20.9 species when the marsh was restricted to 13.0 species. Total nekton density did not change with restoration, but shifts in community composition were evident. In this study restoration induced rapid changes in the composition, density, size, and distribution of nekton species, but additional monitoring is necessary to quantify longer‐term effects of salt marsh restoration on nekton.     

Tidal Marsh Restoration: Trends in Vegetation Change Using a Geographical Information System (GIS)

Adequately evaluating the success of coastal tidal marsh restoration has lagged behind the actual practice of restoring tidally restricted salt marshes. A Spartina-dominated valley marsh at Barn Island Wildlife Management Area, Stonington, Connecticut, was tidally restricted in 1946 and consequently converted mostly to Typha angustifolia. With the re-introduction of tidal flooding in 1978, much of the marsh has reverted to Spartina alterniflora. Using a geographical information system (GIS), this study measures restoration success by the extent of geographical similarity between the vegetation of the restored marsh and the pre-impounded marsh. Based on geographical comparisons among different hydrologic states, pre-impounded (1946), impounded (1976), and restored (1988) tidal marsh restoration is a convergent process. Although salt marsh species currently dominate the restored system, the magnitude of actual agreement between the pre-impounded vegetation and that of the restored marsh is only moderate. Further restoration of the salt marsh vegetation may be limited by continued tidal restriction, marsh surface subsidence, and reduced accretion rates. General trends of recovery are identified using a gradient approach and the geographic pattern’ of vegetation change. In the strictest sense, if restoration refers only to vegetation types that geographically replicate preexisting types, then only 28% of the marsh has been restored. Restoration in a broader sense, however, representing the original salt marsh vegetation regardless of spatial position, amounts to 63% restored. Unrestored marsh, dominated by Typha angustifolia and Phragmites australis, remains at 37%. By emphasizing trends during vegetation recovery, this evaluation technique aims to understand the restoration process, direct future research goals, and ultimately aid in future restoration projects.     

Quantifying Vegetation and Nekton Response to Tidal Restoration of a New England Salt Marsh

Tidal flow to salt marshes throughout the northeastern United States is often restricted by roads, dikes, impoundments, and inadequately sized culverts or bridge openings, resulting in altered ecological structure and function. In this study we evaluated the response of vegetation and nekton (fishes and decapod crustaceans) to restoration of full tidal flow to a portion of the Sachuest Point salt marsh, Middletown, Rhode Island. A before, after, control, impact study design was used, including evaluations of the tide‐restricted marsh, the same marsh after reintroduction of tidal flow (i.e., tide‐restored marsh), and an unrestricted control marsh. Before tidal restoration vegetation of the 3.7‐ha tide‐restricted marsh was dominated by Phragmites australis and was significantly different from the adjacent 6.3‐ha Spartina‐dominated unrestricted control marsh (analysis of similarities randomization test, p < 0.001). After one growing season vegetation of the tide‐restored marsh had changed from its pre‐restoration condition (analysis of similarities randomization test, p < 0.005). Although not similar to the unrestricted control marsh, Spartina patens and S. alterniflora abundance increased and abundance and height of Phragmites significantly declined, suggesting a convergence toward typical New England salt marsh vegetation. Before restoration shallow water habitat (creeks and pools) of the unrestricted control marsh supported a greater density of nekton compared with the tide‐restricted marsh (analysis of variance, p < 0.001), but after one season of restored tidal flow nekton density was equivalent. A similar trend was documented for nekton species richness. Nekton density and species richness from marsh surface samples were similar between the tide‐restored marsh and unrestricted control marsh. Fundulus heteroclitus and Palaemonetes pugio were the numerically dominant fish and decapod species in all sampled habitats. This study provides an example of a quantitative approach for assessing the response of vegetation and nekton to tidal restoration.     

Ecological responses to tidal restorations of two northern New England salt marshes

Efforts are underway to restore tidal flow in New England salt marshes that were negatively impacted by tidal restrictions. We evaluated a planned tidal restoration at Mill Brook Marsh (New Hampshire) and at Drakes Island Marsh (Maine) where partial tidal restoration inadvertently occurred. Salt marsh functions were evaluated in both marshes to determine the impacts from tidal restriction and the responses following restoration. Physical and biological indicators of salt marsh functions (tidal range, surface elevations, soil water levels and salinities, plant cover, and fish use) were measured and compared to those from nonimpounded reference sites. Common impacts from tidal restrictions at both sites were: loss of tidal flooding, declines in surface elevation, reduced soil salinity, replacement of salt marsh vegetation by fresh and brackish plants, and loss of fish use of the marsh. Water levels, soil salinities and fish use increased immediately following tidal restoration. Salt-intolerant vegetation was killed within months. After two years, mildly salt-tolerant vegetation had been largely replaced in Mill Brook Marsh by several species characteristic of both high and low salt marshes. Eight years after the unplanned, partial tidal restoration at Drakes Island Marsh, the vegetation was dominated bySpartina alterniflora, a characteristic species of low marsh habitat. Hydrologic restoration that allowed for unrestricted saltwater exchange at Mill Brook restored salt marsh functions relatively quickly in comparison to the partial tidal restoration at Drakes Island, where full tidal exchange was not achieved. The irregular tidal regime at Drakes Island resulted in vegetation cover and patterns dissimilar to those of the high marsh used as a reference. The proper hydrologic regime (flooding height, duration and frequency) is essential to promote the rapid recovery of salt marsh functions. We predict that functional recovery will be relatively quick at Mill Brook, but believe that the habitat at Drakes Island will not become equivalent to that of the reference marsh unless the hydrology is further modified.     

Ecological responses to tidal restorations of two northern New England salt marshes

Efforts are underway to restore tidal flow in New England salt marshes that were negatively impacted by tidal restrictions. We evaluated a planned tidal restoration at Mill Brook Marsh (New Hampshire) and at Drakes Island Marsh (Maine) where partial tidal restoration inadvertently occurred. Salt marsh functions were evaluated in both marshes to determine the impacts from tidal restriction and the responses following restoration. Physical and biological indicators of salt marsh functions (tidal range, surface elevations, soil water levels and salinities, plant cover, and fish use) were measured and compared to those from nonimpounded reference sites. Common impacts from tidal restrictions at both sites were: loss of tidal flooding, declines in surface elevation, reduced soil salinity, replacement of salt marsh vegetation by fresh and brackish plants, and loss of fish use of the marsh.Water levels, soil salinities and fish use increased immediately following tidal restoration. Salt-intolerant vegetation was killed within months. After two years, mildly salt-tolerant vegetation had been largely replaced in Mill Brook Marsh by several species characteristic of both high and low salt marshes. Eight years after the unplanned, partial tidal restoration at Drakes Island Marsh, the vegetation was dominated bySpartina alterniflora, a characteristic species of low marsh habitat.Hydrologic restoration that allowed for unrestricted saltwater exchange at Mill Brook restored salt marsh functions relatively quickly in comparison to the partial tidal restoration at Drakes Island, where full tidal exchange was not achieved. The irregular tidal regime at Drakes Island resulted in vegetation cover and patterns dissimilar to those of the high marsh used as a reference. The proper hydrologic regime (flooding height, duration and frequency) is essential to promote the rapid recovery of salt marsh functions. We predict that functional recovery will be relatively quick at Mill Brook, but believe that the habitat at Drakes Island will not become equivalent to that of the reference marsh unless the hydrology is further modified.Corresponding Editor: R.E. Turner Manuseript     

Salt Marsh Restoration in Connecticut: 20 Years of Science and Management

In 1980 the State of Connecticut began a tidal marsh restoration program targeting systems degraded by tidal restrictions and impoundments. Such marshes become dominated by common reed grass (Phragmites australis) and cattail (Typha angustifolia and T. latifolia), with little ecological connection to Long Island Sound. The management and scientific hypothesis was that returning tidal action, reconnecting marshes to Long Island Sound, would set these systems on a recovery trajectory. Specific restoration targets (i.e., pre‐disturbance conditions or particular reference marshes) were considered unrealistic. However, it was expected that with time restored tides would return ecological functions and attributes characteristic of fully functioning tidal salt marshes. Here we report results of this program at nine separate sites within six marsh systems along 110 km of Long Island Sound shoreline, with restoration times of 5 to 21 years. Biotic parameters assessed include vegetation, macroinvertebrates, and use by fish and birds. Abiotic factors studied were soil salinity, elevation and tidal flooding, and soil water table depth. Sites fell into two categories of vegetation recovery: slow, ca. 0.5%, or fast, more than 5% of total area per year. Although total cover and frequency of salt marsh angiosperms was positively related to soil salinity, and reed grass stand parameters negatively so, fast versus slow recovery rates could not be attributed to salinity. Instead, rates appear to reflect differences in tidal flooding. Rapid recovery was characterized by lower elevations, greater hydroperiods, and higher soil water tables. Recovery of other biotic attributes and functions does not necessarily parallel those for vegetation. At the longest studied system (rapid vegetation recovery) the high marsh snail Melampus bidentatus took two decades to reach densities comparable with a nearby reference marsh, whereas the amphipod Orchestia grillus was well established on a slow‐recovery marsh, reed grass dominated after 9 years. Typical fish species assemblages were found in restoration site creeks and ditches within 5 years. Gut contents of fish in ditches and on the high marsh suggest that use of restored marsh as foraging areas may require up to 15 years to reach equivalence with reference sites. Bird species that specialize in salt marshes require appropriate vegetation; on the oldest restoration site, breeding populations comparable with reference marshland had become established after 15 years. Use of restoration sites by birds considered marsh generalists was initially high and was still nearly twice that of reference areas even after 20 years. Herons, egrets, and migratory shorebirds used restoration areas extensively. These results support our prediction that returning tides will set degraded marshes on trajectories that can bring essentially full restoration of ecological functions. This can occur within two decades, although reduced tidal action can delay restoration of some functions. With this success, Connecticut's Department of Environmental Protection established a dedicated Wetland Restoration Unit. As of 1999 tides have been restored at 57 separate sites along the Connecticut coast.     

Impacts of plant invasions can be reversed through restoration: a regional meta-analysis of faunal communities

We quantified the effects of invasive Phragmites australis on estuarine faunal communities using meta-analysis to compare invaded to uninvaded marshes and then evaluated whether ecological restoration could reverse those effects. Relative to uninvaded marshes, the quantity and condition of fauna in invaded marshes was significantly poorer. We detected negative impacts to fauna residing in the mid-Atlantic but not in New England and to fauna utilizing the marsh surface but not to those inhabiting tidal creeks. By taxonomic group, we found that the invasion negatively affected nekton but not invertebrates. Both adult and sub-adult nekton were adversely affected, although the magnitude of the effect on the sub-adults was four times greater than that for adults. Our results indicate that negative effects on fauna within the mid-Atlantic region largely drove the overall results. When restored marshes were compared to uninvaded marshes there were no significant differences across all metrics assessed, suggesting that the negative impacts of the invasion were reversed. A separate qualitative review of trophic data indicated that benthic microalgae and dominant vascular plants are important primary producers at the base of the food web in uninvaded, invaded, and restored salt marshes but the overall quantity and importance of microalgae to diet decreased in highly invaded systems due to decreased light, potentially reducing energy availability. Our analyses revealed that while estuarine communities are adversely affected by P. australis, impacts vary by region, habitat, taxonomic group, and life history stage and that restoration can reverse long-term effects over relatively short time scales.     

Tidal‐flow restoration provides little nesting habitat for a globally vulnerable saltmarsh bird

Tidal marshes are among the most threatened habitats on Earth because of their limited natural extent, a long history of human drainage and modification, and anticipated future sea‐level rise. Tidal marshes also provide services to humans and support species of high conservation interest. Consequently, millions of dollars have been spent on tidal marsh restoration throughout North America. Southern New England has a long history of tidal marsh restorations, often focused on removal of the invasive plant Phragmites australis. Working in 18 Connecticut marshes, we examined the bird community in 21 plots in restoration sites and 19 plots in reference sites. Restoration plots were divided into those in marshes where management involved restoring tidal flow and those where direct Phragmites control (e.g. cutting, herbicide) was used. Saltmarsh sparrows Ammodramus caudacutus, which are considered globally vulnerable to extinction, were less common where tidal flow had been restored than at reference sites and nested in only one of 14 tidal‐flow restoration plots. No abundance differences were found for large wading birds, willets Tringa semipalmata, or seaside sparrows Ammodramus maritimus. Vegetation at sites where tidal flow had been restored showed characteristics typical of lower‐elevation marsh, which is unsuitable for nesting saltmarsh sparrows. We conclude that, although tidal‐flow restorations in Connecticut control Phragmites and restore native saltmarsh vegetation, they produce conditions that are largely unsuitable for one of the highest conservation priority species found in eastern U.S. salt marshes.     

Overwintering habitat selection by the mummichog, Fundulus Heteroclitus, in a Cape Cod (USA) salt marsh

This study tracked the seasonal distribution and winter habitat selection of the mummichog, Fundulus heteroclitus (Linnaeus), in a Cape Cod, Massachusetts salt marsh. Fish (mean size = 43.1 mm total length, range = 10–93 mm) were collected with a 1 m² throw trap and by excavating sediments. In fall, F. heteroclitus began migrating upstream in creeks and eventually moved into upstream pools where they remained throughout winter. F. heteroclitus burrowed into the sediments of these pools at a density of 0.5 fish m^–2, but was not found burrowed in the sediments of downstream pools or any creeks. Sediments in upstream pools were composed of a higher proportion of fine-grained particles and organic content than other marsh pools and creeks, and winter temperatures in upstream pool sediments remained above 1 °C. Temperatures in the water column and sediments of downstream pools regularly dropped below –1.8 °C, exceeding the lethal limit for F. heteroclitus. These results support other recent work showing that F. heteroclitus migrates upstream in salt marshes in fall and overwinters in salt marsh pools. Moreover, this study demonstrates that F. heteroclitus does not utilize all available pools as overwintering habitat but apparently selects pools with sediments that offer a thermal refuge from lethal winter temperatures.     

The Role of Fundulus heteroclitus in Salt Marsh Trophic Dynamics

The common mummichog, Fundulus heteroclitus, functions as bothpredator and prey in the trophic structure of east coast tidalmarshes. Although mummichogs are generally considered importantto energy transformations within marshes, few studies have convincinglydemonstrated that predation by F. heteroclitus affects the abundanceof salt marsh benthic invertebrates. Thus far investigationsof this type have dealt only with the direct effects of adultmummichogs. The results of recent experiments have suggestedthat by controlling smaller predators, mummichogs may indirectlyhave a positive effect on the densities of some infaunal marshinvertebrates. Our current knowledge of larval and juvenilemummichogs in their natural habitat is minimal. Unlike the adults,which can utilize the intertidal zone only when it is flooded,the young remain on the marsh even at low tide, inhabiting shallowpuddles of residual tidal water that form between clumps ofvegetation and around fiddler crab (Uca sp.) burrows. The importanceof F. heteroclitus in salt marsh communities will remain incompletelyunderstood unless future studies consider the role of larvaland juvenile mummichogs. Although many species of fishes andwading birds feed on mummichogs, the blue crab (Callinectessapidus) is probably the major predator of adult F. heteroclitusin the intertidal salt marsh. Predation by adult mummichogsand xanthid crabs (e.g., Eurytium limosum) may contribute tothe high mortality of larval and juvenile Fundulus.     

Macro‐Tidal Salt Marsh Ecosystem Response to Culvert Expansion

The purpose of this paper was to examine the vegetative, sedimentary, nekton and hydrologic conditions pre‐restoration and the initial 2 years post‐restoration at a partially restricted macro‐tidal salt marsh site. Replacement of the culvert increased tidal flow by 88%. This was instrumental in altering the geomorphology of the site, facilitating the creation of new salt marsh pannes, expansion of existing pannes in the mid and high marsh zones, and expansion of the tidal creek network by incorporating relict agricultural ditches. In addition, the increase in area flooded resulted in a significant increase in nekton use, fulfilling the mandate of a federal habitat compensation program to increase and improve the overall availability and accessibility of fish habitat. The restoration of a more natural hydrological regime also resulted in the die‐off of freshwater and terrestrial vegetation along the upland edge of the marsh. Two years post‐restoration, Salicornia europea (glasswort) and Atriplex glabriuscula (marsh orache), were observed growing in these die‐back areas. Similar changes in the vegetation community structure were not observed at the reference site; however, the latter did contain higher species richness. This study represents the first comprehensive, quantitative analysis of ecological response to culvert replacement in a hypertidal ecosystem. These data will contribute to the development of long‐term data sets of pre‐ and post‐restoration, and reference marsh conditions to determine if a marsh is proceeding as expected, and to help with models that are aimed at predicting the response of marshes to tidal restoration at the upper end of the tidal spectrum.     

Piscivory by the mummichog (Fundulus heteroclitus): Evidence from the laboratory and salt marshes

While piscivory is common in many fishes, there are few accounts for the fundulid, Fundulus heteroclitus (mummichog). We suspected that this species might be involved in several forms of piscivory including predation, cannibalism and scavenging. To evaluate these possibilities we conducted several laboratory experiments and field observations in its primary habitat, salt marshes. We found that digestion of larvae and small juveniles of F. heteroclitus was fast (< 1 h) and this makes detection of small fish prey difficult for any form of piscivory. In addition, laboratory experiments (one-on-one encounters, feeding on dead prey) indicated that both cannibalism and scavenging of conspecific prey were possible. Field observations (n = 2449 stomachs from fish 12-106 mm TL over four years at two salt marshes) also suggested that piscivory occurred frequently (4.3-24.7% of stomachs examined) based on the detection of numerous fish hard parts, especially pharyngeal jaws. These structures allowed us to determine that most prey were F. heteroclitus and to back-calculate the size of the prey and thus the piscivore/prey size relationship. As a result, it appears that both cannibalism (0.2-9.1% of stomachs) and scavenging (0.5-9.9%) are common feeding modes of F. heteroclitus in salt marshes and, subsequently, modes of energy transfer for salt marshes in general. We suggest that future studies of fish feeding consider that cannibalism and scavenging may be frequent possibilities when fish remains are detected in stomach contents.     

Movements and growth of tagged young-of-the-year Atlantic croaker (Micropogonias undulatus L.) in restored and reference marsh creeks in Delaware Bay, USA

The residence time, movements, and growth of tagged young-of-the-year Atlantic croaker, Micropogonias undulatus L., were studied from July to October 1998 as measures of the success of a marsh restoration project adjacent to Delaware Bay. A total of 8173 croaker (41-121 mm SL) were tagged from each of two creeks in both marshes during July and August with internal sequential coded wire microtags. A prior tag-retention study in the laboratory found a 95% tag retention rate. Of those tagged, 3.6% were recaptured within and nearby the study creeks using seines, otter trawls, and weirs during a 105-day period. Recapture percentages ranged from 1.5% to 6.1% in individual creeks in the restored marsh. There was some movement of tagged fish between creeks in the restored marsh and out into the main creek, but 95% of the recaptures were made in the subtidal and intertidal portions of the same creek in which they were tagged. Fewer fish were recaptured at the reference marsh (1.6% recapture; n=1489 tagged) up to 50 days after tagging, with no evidence of movement between creeks. The average individual growth rates for recaptured croaker was the same in both restored (0.69 mm/day) and reference (0.63 mm/day) marshes before egress from the creeks in September and October. As a result, both created creeks in a restored marsh and natural creeks in a reference marsh appeared to be utilized as young-of-the-year habitat in a similar way during the summer and until egress out of the marshes during the fall, thus this restoration effort has been successful in creating suitable habitat for Atlantic croaker.     

Patterns in the utilization of the intertidal salt marsh by larvae and juveniles of Fundulus heteroclitus (Linnaeus) and Fundulus luciae (Baird)

Larval and juvenile fishes were collected at low tide from the surface of an intertidal salt marsh on Sapelo Island, Georgia every 6 days from 25 May through 20 December 1982. Larval fishes were present in shallow puddles of tidal water on the marsh from the beginning of the sampling period until the end of October. Juveniles were present throughout the year. Fundulus heteroclitus (Linnaeus) and F. luciae (Baird) accounted for 96.3% (67.0% and 29.3%, respectively) of the 4355 fishes collected. These fishes exhibited synchronous, temporal pulses in larval abundance, suggesting that reproduction was discontinuous and controlled by the same factor(s) in both species. Larval F. heteroclitus inhabited aquatic micro-habitats near the upland edge of the intertidal marsh, but as the larvae grew to juvenile size (≈ 10 mm standard length) they moved to lower elevations near a tidal creek. Large juveniles and adults of F. heteroclitus infrequently occurred in the samples, presumably because they leave the intertidal marsh as the tide ebbs. F. luciae were rarely found in low marsh areas, but all age classes (including adults) occurred at higher elevations, supporting previous suggestions that this species prefers high marsh habitats. The vegetated, intertidal salt marsh appears to be the principal nursery habitat for both of these cyprinodontid species.     

The natural regeneration of salt marsh on formerly reclaimed land

Question: Does the vegetation of restored salt marshes increasingly resemble natural reference communities over time? Location: The Essex estuaries, southeast England. Methods: Abandoned reclamations, where coastal defences had been breached in storm events, and current salt marsh recreation schemes were surveyed giving a chronosequence of salt marsh regeneration from 2 to 107 years. The presence, abundance and height of plant species were recorded and comparisons were made with adjacent reference salt marsh communities at equivalent elevations. Results: Of the 18 paired sites surveyed, 13 regenerated marshes had fewer species than their adjacent reference marsh, three had an equal number and two had more. The plant communities of only two de‐embankment sites matched that of the reference community. 0–50 year old sites and 51–100 year old sites had fewer species per quadrat than the 101+ year sites and the reference salt marshes. There was a weak relationship between differences in species richness for regenerated and reference marshes and the time since sites were first re‐exposed to tidal inundation. Cover values for the invasive and recently evolved Spartina anglica were greater within regenerated than reference marshes. Conclusions: Salt marsh plants will colonise formerly reclaimed land relatively quickly on resumption of tidal flooding. However, even after 100 years regenerated salt marshes differ in species richness, composition and structure from reference communities.     

Phragmites australis and silica cycling in tidal wetlands

Tidal marshes have recently been shown to be important biogenic Si recycling surfaces at the land–sea interface. The role of vegetation in this recycling process has not yet been quantified. In situ and ex situ decomposition experiments were conducted with Phragmites australis stems. In a freshwater tidal marsh, litterbags were incubated at different elevations and during both winter and summer. Biogenic Si (BSi) dissolution followed a double exponential decay model in the litterbags (from ca. 60 to 15 mg g⁻¹ after 133 days), irrespective of season. Si was removed much faster from the incubated plant material compared to N and C, resulting in steadily decreasing Si/N and Si/C ratios. Ex situ, decomposition experiments were conducted in estuarine water, treated with a broad-spectrum antibiotic, and compared to results from untreated incubations. The bacterial influence on the dissolution of dissolved Si (DSi) from P. australis stems was negligible. Although the rate constant for dissolved Si dissolution decreased from 0.004 to 0.003 h⁻¹, the eventual amount of BSi dissolved and saturation concentration in the incubation environment were similar in both treatments. P. australis contributes to and enhances dissolved Si recycling capacity of tidal marshes: in a reed-dominated small freshwater tidal marsh, more than 40% of DSi export was attributable to reed decomposition. As the relation between tidal marsh surface and secondary production in estuaries has been linked to marsh Si cycling capacity, this provides new insight in the ecological value of the common reed.     

Utilization of a citizen monitoring protocol to assess the structure and function of natural and stabilized fringing salt marshes in North Carolina

Narrow fringing salt marshes dominated by Spartina alterniflora occur naturally along estuarine shorelines and provide many of the same ecological functions as more extensive marshes. These fringing salt marshes are sometimes incorporated into shoreline stabilization efforts. We obtained data on elevation, salinity, sediment characteristics, vegetation and fish utilization at three study sites containing both natural fringing marshes and nearby restored marshes located landward of a stone sill constructed for shoreline stabilization. During the study, sediment accretion rates in the restored marshes were approximately 1.5- to 2-fold greater than those recorded in the natural marshes. Natural fringing marsh sediments were predominantly sandy with a mean organic matter content ranging between 1.5 and 6.0%. Average S. alterniflora stem density in natural marshes ranged between 130 and 222 stems m⁻², while mean maximum stem height exceeded 64 cm. After 3 years, one of the three restored marshes (NCMM) achieved S. alterniflora stem densities equivalent to that of the natural fringing marshes, while percentage cover and maximum stem heights were significantly greater in the natural than in the restored marshes at all sites. There was no significant difference in the mean number of fish, crabs or shrimp captured with fyke nets between the natural and restored marshes, and only the abundance of Palaemonetes vulgaris (grass shrimp) was significantly greater in the natural marshes than in the restored ones. Mean numbers of fish caught per 5 m of marsh front were similar to those reported in the literature from marshes adjacent to tidal creeks and channels, and ranged between 509 and 634 fish net⁻¹. Most of the field data and some of the sample analyses were obtained by volunteers as they contributed 223 h of the total 300 h spent collecting data from three sites in one season. The use of fyke nets required twice as many man-hours as any other single task. Vegetation and sediment parameters were sensitive indicators of marsh restoration success, and volunteers were capable of contributing a significant portion of the labor needed to collect these parameters. The U.S. Government's right to retain a non-exclusive, royalty-free license in and to any copyright is acknowledged.     

Role of biotic interactions and physical factors in determining the distribution of marsh species along an estuarine salinity gradient

Understanding the mechanisms that shape plant distribution patterns is a major goal in ecology. We investigated the role of biotic interactions (competition and facilitation) and abiotic factors in creating horizontal plant zonation along salinity gradients in the Elbe estuary. We conducted reciprocal transplant experiments with four dominant species from salt and tidal freshwater marshes at two tidal elevations. Ten individuals of each species were transplanted as sods to the opposing marsh type and within their native marsh (two sites each). Transplants were placed at the centre of 9‐m² plots along a line parallel to the river bank. In order to disentangle abiotic and biotic influences, we set up plots with and without neighbouring vegetation, resulting in five replicates per site. Freshwater species (Bolboschoenus maritimus and Phragmites australis) transplanted to salt marshes performed poorly regardless of whether neighbouring vegetation was present or not, although 50–70% of the transplants did survive. Growth of Phragmites transplants was impaired also by competition in freshwater marshes. Salt marsh species (Spartina anglica and Puccinellia maritima) had extremely low biomass when transplanted to freshwater marshes and 80–100% died in the presence of neighbours. Without neighbours, biomass of salt marsh species in freshwater marshes was similar to or higher than that in salt marshes. Our results indicate that salt marsh species are precluded from freshwater marshes by competition, whereas freshwater species are excluded from salt marshes by physical stress. Thus, our study provides the first experimental evidence from a European estuary for the general theory that species boundaries along environmental gradients are determined by physical factors towards the harsh end and by competitive ability towards the benign end of the gradient. We generally found no significant impact of competition in salt marshes, indicating a shift in the importance of competition along the estuarine gradient.