Responses of Salt Marsh Ecosystems to Mosquito Control Management Practices along the Atlantic Coast (U.S.A.)

Open marsh water management (OMWM) of salt marshes modifies grid‐ditched marshes by creating permanent ponds and radial ditches in the high marsh that reduce mosquito production and enhance fish predation on mosquitoes. It is preferable to using pesticides to control salt marsh mosquito production and is commonly presented as a restoration or habitat enhancement tool for grid‐ditched salt marshes. Monitoring of nekton, vegetation, groundwater level, soil salinity, and bird communities before and after OMWM at 11 (six treatment and five reference sites) Atlantic Coast (U.S.A.) salt marshes revealed high variability within and among differing OMWM techniques (ditch‐plugging, reengineering of sill ditches, and the creation of ponds and radial ditches). At three marshes, the dominant nekton shifted from fish (primarily Fundulidae species) to shrimp (Palaemonidae species) after manipulations and shrimp density increased at other treatment sites. Vegetation changed at only two sites, one with construction equipment impacts (not desired) and one with a decrease in woody vegetation along existing ditches (desired). One marsh had lower groundwater level and soil salinity, and bird use, although variable, was often unrelated to OMWM manipulations. The potential effects of OMWM manipulations on non‐target salt marsh resources need to be carefully considered by resource planners when managing marshes for mosquito control.     

Are biotic factors significant in influencing the distribution of halophytes in saline habitats?

The influence of biotic factors on the distribution and establishment of halophytes is being considered in this review. Physicochemical factors, such as salinity and flooding, often are considered to be the determining factors controlling the establishment and zonational patterns of species in salt marsh and salt desert environments. Sharp boundaries commonly are found between halophyte communities even though there is a gradual change in the physicochemical environment, which indicates that biotic interactions may play a significant role in deterining the distribution pattern of species and the composition of zonal communities. Competition is hypothesized to play a key role in determining both the upper and lower limits of species distribution along a salinity gradient. Field and laboratory experiments indicate that the upper limits of distribution of halophytes into less saline or nonsaline habitats is often determined by competition. There appears to be a reciprocal relationship between the level of salt tolerance of species and their ability to compete with glycophytes in less saline habitats. Halophytes are not competitive in nonsaline habitats, but their competitive ability increases sharply in saline habitats. Allelopathic effects have been reported in salt desert habitats, but have not been reported along salinity gradients in salt marshes. Some species of halophytes that are salt accumulators have the ability to change soil chemistry. Chemical inhibition of intolerant species occurs when high concentrations of sodium are concentrated in the surface soils of salt desert plant communities that are dominated by salt-accumulating species. Establishment of less salt-tolerant species is inhibited in the vicinity of these salt-accumulating species. Herbivory is reported to cause both an increase and a decrease in plant diversity in salt marsh habitats. Heavy grazing is reported to eliminate sensitive species and produce a dense cover of graminoids in high marsh coastal habitats. However, in other marshes, grazing produced bare patches that allowed annuals and other low marsh species to invade upper marsh zonal communities. A retrogression in plant succession may occur in salt marshes and salt deserts because of heavy grazing. Intermediate levels of grazing by sheep, cattle, and horses could produce communities with the highest species richness and heterogeneity. Grazing by geese produced bare areas that had soils with higher salinity and lower soil moisture than vegetated areas, allowing only the more salt-tolerant species to persist. Removal of geese from areas by use of inclosures caused an increase in species richness in subarctic salt marshes. Invertebrate herbivores could also inhibit the survival of seeds and the ability of plants to establish in marshes. Parasites could play a significant role in determining the species composition of zonal communities, because uninfected rarer species are able to establish in the gaps produced by the death of parasitized species.     

Ditches as species‐rich secondary habitats and refuge for meadow species in agricultural marsh grasslands

Questions

Can drainage ditches in agricultural marsh grassland provide a suitable habitat for the persistence of fen meadow species? How does the ditch margin vegetation develop as a function of regular dredging? Is ornithologically oriented management also beneficial for plant biodiversity?

Location

Riparian marshes, Eider‐Treene‐Sorge lowland, Schleswig‐Holstein, Germany.

Methods

We performed vegetation surveys of drainage ditches along with their water body, slope and margin structures annually for 3 years. The data were analysed with respect to date and means of ditch dredging. In addition, we recorded vegetation of the surrounding agricultural grassland, measured nutrient status of the soil and the water body and sampled seed bank of the ditch slopes. We used ANOVA and multivariate methods to describe the development of the ditch vegetation and the persistence of target meadow species.

Results

Vegetation re‐development of ditch margins proceeds quite rapidly after disturbance from dredging. Dominance of mudbank species was observed only in the first year, followed by an increase of reed species and reduction of phytodiversity. Target species of wet meadow communities reach highest abundance in the second and third year and build a significant seed bank before being suppressed by reeds.

Conclusions

In heavily eutrophicated, intensively used marsh grassland, regularly disturbed ditch margins are important secondary habitats for pioneer and subdominant wetland species, which have nearly disappeared in a larger area. Current management cycles of ditch dredging every 3–4 years comply with the successional development, allowing the mudbank and wet meadow species to persist in the vegetation and seed bank. In contrast to the frequency, the form of dredging (ditch profile), which is crucial for bird protection, plays a minor role for plants. We recommend moderate disturbance (mowing of ditch margins) to suppress strong competitors in the years between dredging for additional support to target plant species.     

陕西省黄河中游湿地冬季鸭科鸟类群落结构

2002～2007年冬季,对黄河中游湿地4种典型生境包括滩涂、人工渔塘、芦苇沼泽和莲池中的鸭科鸟类群落进行了调查.共记录到鸭科鸟类7属20种,采用频率指数法确定的优势种为斑嘴鸭、绿翅鸭、赤膀鸭、绿头鸭、普通秋沙鸭,其数量之和占总数量的65.6%.对4种不同生境的物种多样性、丰富度、均匀度、优势度进行分析,结果表明芦苇沼泽的多样性和丰富度指数最高,莲池的多样性和丰富度指数最低.人类活动引起的隐蔽场所和食物资源的变化是造成分布差异的主要原因.     

Composition and abundance of resident marsh-surface nekton: comparison between tidal freshwater and salt marshes in Virginia,USA

Previous research on intertidal nekton communities has identifiedimportant determinants of community structure and distribution; however, fewstudies have compared nekton utilization of disparate marsh habitats. Inthis study, abundance and distribution patterns of resident nekton werecompared between tidal freshwater marsh and salt marsh surfaces varying inflooding depth and duration. Nekton were collected in pit traps installedalong elevational transects at four marshes in coastal Virginia (twofreshwater, two saline) from April through November 1992–1993. Thedominant fish collected at all sites was the mummichog Fundulusheteroclitus. The daggerblade grass shrimp Palaemonetes pugio was thedominant nekton species collected at salt marsh sites, and was seasonallyabundant on tidal freshwater marshes. A positive correlation betweenflooding depth and nekton abundance was observed on salt marshes; anopposite pattern was observed on tidal freshwater marshes. Tidal floodingregime influences the abundance of resident nekton, however, the effect maybe confounded by other environmental variables, including variation insurface topography and seasonal presence or absence of submerged aquaticvegetation (SAV) in adjacent subtidal areas. In mid-Atlantic tidalfreshwater wetlands, SAV provides a predation refuge and forage site forearly life stages of marsh-dependent nekton, and several species utilizethis environment extensively. Salt marshes in this region generally lackdense SAV in adjacent subtidal creeks. Consequently, between-sitedifferences in species and size-specific marsh surface utilization byresident nekton were observed. Larvae and juveniles represented 79%and 59% of total fish collected at tidal freshwater and salt marshsites, respectively. The resident nekton communities of tidal freshwater andsalt marsh surfaces are characterized by a few ubiquitous species with broadenvironmental tolerances. This revised version was published online in July 2006 with corrections to the Cover Date.     

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.     

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.     

Changes in marsh nekton communities along the salinity gradient of the Schelde river, Belgium and The Netherlands

Nekton was sampled in five marshes along the salinity gradient of the Schelde River. The utilisation of three different habitats (large and small creek, marsh pond) by fish and macrocrustacean species was compared among the five sampling sites. In the larger channels fyke nets were deployed to capture fish and macrocrustaceans leaving the marsh at ebb while block nets were set in smaller intertidal creeks. Fish traps passively sampled fish and shrimp in the marsh ponds. The tidal freshwater marsh had a species poor fauna and only a low number of fish was caught. Besides some freshwater species (Alburnoides bipunctatus, Carassius carassius) the European eel, Anguilla anguilla was still present. The four other marshes had a similar community structure although Platichthys flesus was absent from the euhaline area. Among fish species, dominance of Dicentrarchus labrax, Platichthys flesus and Pomatoschistus microps was observed. Carcinus maenas and Palaemonetes varians were the most abundant macrocrustacean species in every marsh. Between the large and small intertidal creeks there was no difference in nekton species composition. The main species used both habitats. Marsh ponds were utilized intensively only by two species, Pomatoschistus microps and Palaemonetes varians in every marsh.     

A vegetation zonation from saltmarsh to riverbank in New Zealand

Abstract. Brackish riverbank marshes have been little studied. Therefore, a plant community sequence was sampled from saltmarsh to near-freshwater riverbank marsh on a number of disjunct marshes along the Taieri River, Otago, New Zealand, from near the mouth to 9 km inland. Salinity decreased steadily upstream, though the actual values were very different on two days sampled. Ten communities are recognised. The major vegetation zonation was upshore more than upstream, though there were several interactions between the upshore and upstream gradients. Few species, if any, were restricted to the mid reaches of the length of river sampled. There was only a very slight upshore increase in species richness, and no trend upstream. Sequences of communities occurred upshore on all marshes, but the sequence differed, even within a marsh. Species were assorted into communities in different ways from those of marine marshes in the area. Some species, native and exotic, occupied different beta-niches from those they occupied in other countries. Individualistic community structure is inferred.