Incomplete recovery of plant diversity in restored prairie wetlands on agricultural landscapes

Restoration efforts are being implemented globally to mitigate the degradation and loss of wetland habitat; however, the rate and success of wetland vegetation recovery post‐restoration is highly variable across wetland classes and geographies. Here, we measured the recovery of plant diversity along a chronosequence of restored temporary and seasonal prairie wetlands ranging from 0 to 23 years since restoration, including drained and natural wetlands embedded in agricultural and natural reserve landscapes in central Alberta, Canada. We assessed plant diversity using the following structural indicators: percent cover of hydrophytes, native and non‐native species, species richness, and community composition. Our findings indicate that plant diversity recovered to resemble reference wetlands in agricultural landscapes within 3–5 years of restoration; however, restored wetlands maintained significantly lower species richness and a distinct community composition compared to reference wetlands located within natural reserves. Early establishment of non‐native species during recovery, dispersal limitation, and depauperated native seed bank were probable barriers to complete recovery. Determining the success of vegetation recovery provides important knowledge that can be used to improve restoration strategies, especially considering projected future changes in land use and climate.     

Hydrologic similarity to reference wetlands does not lead to similar plant communities in restored wetlands

Few wetland restoration projects include long‐term hydrologic and floristic data collection, limiting our understanding of community assembly over restored hydrologic gradients. Although reference sites are commonly used to evaluate outcomes, it remains unclear whether restoring similar water levels to reference sites also leads to similar plant communities. We evaluated long‐term datasets from reference and restored wetlands 15 years after restoration to test whether similar water levels in reference and restored sites led to vegetation similarity. We compared the hydrologic regimes for three different wetland types, tested whether restored wetland water levels were different from reference water levels, and whether hydrologic similarity between reference and restored wetlands led to similarity in plant species composition. We found restored wetlands had similar water levels to references 15 years after restoration, and that species richness was higher in reference than restored wetlands. Vegetation composition was similar across all wetland types and was weakly correlated to wetland water levels overall. Contrary to our hypothesis, water table depth similarity between restored and reference wetlands did not lead to similar plant species composition. Our results highlight the importance of the initial planting following restoration and the importance of hydrologic monitoring. When the restoration goal is to create a specific wetland type, plant community composition may not be a suitable indicator of restoration progress in all wetland types.     

Initial soil amendments still affect plant community composition after nine years in succession on a heavy metal contaminated mountainside

Many efforts to restore disturbed landscapes seek to meet ecological goals over timescales from decades to centuries. It is thus crucial to know how different actions available to restoration practitioners may affect ecosystems in the long term, yet few such data exist. Here, we test the effects of seed and compost applications on plant community composition 9 years after their application, by taking advantage of a well‐controlled restoration experiment on a mountainside severely degraded by over 80 years of zinc smelting emissions. We asked whether plots have converged on similar plant communities regardless of initial seed and compost treatments, or if these initial treatments have given rise to lasting differences in whole plant communities or in the richness and abundance of native, exotic, and planted species. We found that compost types significantly affected plant communities 9 years later, but seed mix species composition did not. Observed differences in species richness and vegetative cover were negatively correlated, and both were related to the differences in plant communities associated with different compost types. These observed differences are due primarily to the number and abundance of species not in original seed mixes, of which notably many are native. Our results underscore the importance of soils in shaping the aboveground composition of ecosystems. Differences in soil characteristics can affect plant diversity and cover, which are both common restoration targets. Even in highly polluted and devegetated sites, compost and seed application can reinstate high vegetative cover and allow continued colonization of native species.     

A comparison of created and natural wetlands in Pennsylvania,USA

Recent research suggests that created wetlands do not look, or function, like the natural systems they are intended to replace. Proper planning, construction, and the introduction of appropriate biotic material should initiate natural processes which continue indefinitely in a successful wetland creation project, with minimal human input. To determine if differences existed between created and natural wetlands, we compared soil matrix chroma, organic matter content, rock fragment content, bulk density, particle size distribution, vegetation species richness, total plant cover, and average wetland indicator status in created (n = 12) and natural (n = 14)wetlands in Pennsylvania (USA). Created wetlands ranged in age from two to 18 years. Soils in created wetlands had less organic matter content, greater bulk densities, higher matrix chroma, and more rock fragments than reference wetlands. Soils in reference wetlands had clay loam textures with high silt content, while sandy clay loam textures predominated in the created sites. Vegetation species richness and total cover were both greater in natural reference wetlands. Vegetation in created wetlands included a greater proportion of upland species than found in the reference wetlands. There were significant differences in soils and vegetation characteristics between younger and older created wetlands, though we could not say older created sites were trending towards the reference wetland condition. Updated site selection practices, more careful consideration of monitoring period lengths, and, especially, a stronger effort to recreate wetland types native to the region should result in increased similarity between created and natural wetlands.     

Vegetation Similarity and Avifaunal Food Value of Restored and Natural Marshes in Northern New York

Measuring the success of wetland restoration efforts requires an assessment of the wetland plant community as it changes following restoration. But analyses of restored wetlands often include plant community data from only one time period. We studied the development of plant communities at 13 restored marshes in northern New York for 4 years, including 1 year prior to restoration and 3 years afterwards. Restored wetlands ranged in size from 0.23 to 1.70 ha. Four reference wetlands of similar basin morphology, soil type, and size (0.29–0.48 ha) that occurred naturally in the same area were studied as comparisons. Dike construction to restore hydrology disturbed the existing vegetation in some parts of the restored sites, and vegetation was monitored in both disturbed and undisturbed areas. Undisturbed areas within the restored sites, which were dominated by upland field grasses before restoration, developed wetland plant communities with lower wetland index values but comparable numbers of wetland plant species than the reference wetlands, and they lagged behind the reference sites in terms of total wetland plant cover. There were significantly more plant species valuable as food sources for wetland birds, and a significantly higher percent cover of these species, at the undisturbed areas of the restored sites than at the reference wetlands. Areas of the restored sites that were disturbed by dike construction, however, often developed dense, monospecific cattail stands. In general, the plant communities at restored sites became increasingly similar to those at the reference wetlands over time, but higher numbers of herbaceous plants developed at the restored sites, including food plants for waterfowl, rails, and songbirds. Differences in shrub cover will probably lessen as natural recolonization increases shrub cover at the restored sites. Natural recolonization appears to be an effective technique for restoring wetlands on abandoned agricultural fields with established plant cover, but it is less successful in areas where soil has been exposed by construction activity.     

How Does Restoration of Native Canopy Affect Understory Vegetation Composition? Evidence from Riparian Communities of the Hunter Valley Australia

Restoration of native vegetation often focuses on the canopy layer species, with the assumption that regeneration of the understory elements will occur as a consequence. The goal of this study was to assess the influence of canopy restoration on the composition and abundance of understory plant species assemblages along riparian margins in the Hunter Valley, NSW, Australia. We compared the floristic composition (richness, abundance, and diversity) of understory species between nonrevegetated (open) and canopy revegetated plots across five sites. A number of other factors that may also influence understory vegetation, including soil nutrients, proximity to main channel, and light availability, were also measured. We found that sites where the canopy had been restored had lower exotic species richness and abundance, as well as higher native species cover, but not native species richness, compared with open sites. Multivariate analysis of plots based on plant community composition showed that revegetated sites were associated with lower total species diversity, light availability, and exotic cover. This study has found that the restoration of the canopy layer does result in lower exotic species richness and cover, and higher native species cover and diversity in the understory, a desirable restoration outcome. Our results provide evidence that restoration of native canopy species may facilitate restoration of native understory species; however, other interventions to increase native species richness of the understory should also be considered as part of management practice.     

Recovery of Native Plant Community Characteristics on a Chronosequence of Restored Prairies Seeded into Pastures in West‐Central Iowa

Restored grasslands comprise an ever‐increasing proportion of grasslands in North America and elsewhere. However, floristic studies of restored grasslands indicate that our ability to restore plant communities is limited. Our goal was to assess the effectiveness of restoration seeding for recovery of key plant community components on former exotic, cool‐season pastures using a chronosequence of six restoration sites and three nearby remnant tallgrass prairie sites in West‐Central Iowa. We assessed trends in Simpson's diversity and evenness, richness and abundance of selected native and exotic plant guilds, and mean coefficient of conservatism (mean C). Simpson's diversity and evenness and perennial invasive species abundance all declined with restoration site age. As a group, restoration sites had greater richness of native C₃ species with late phenology, but lower richness and abundance of species with early phenology relative to remnant sites. Total native richness, total native abundance (cover), mean C, and abundance of late phenology C₃ plants were similar between restoration and remnant sites. Observed declines in diversity and evenness with restoration age reflect increases in C₄ grass abundance rather than absolute decreases in the abundance of perennial C₃ species. In contrast to other studies, restoration seeding appears to have led to successful establishment of tallgrass prairie species that were likely to be included in seeding mixtures. While several floristic measures indicate convergence of restoration and remnant sites, biodiversity may be further enhanced by including early phenology species in seeding mixes in proportion to their abundance on remnant prairies.     

Using Functional Trajectories to Track Constructed Salt Marsh Development in the Great Bay Estuary, Maine/New Hampshire, U.S.A.

A growing number of studies have assessed the functional equivalency of restored and natural salt marshes. Several of these have explored the use of functional trajectories to track the increase in restored marsh function over time; however, these studies have disagreed as to the usefulness of such models in long‐term predictions of restored marsh development. We compared indicators of four marsh functions (primary production, soil organic matter accumulation, sediment trapping, and maintenance of plant communities) in 6 restored and 11 reference (matched to restored marshes using principal components analysis) salt marshes in the Great Bay Estuary. The restored marshes were all constructed and planted on imported substrate and ranged in age from 1 to 14 years. We used marsh age in a space‐for‐time substitution to track constructed salt marsh development and explore the use of trajectories. A high degree of variability was observed among natural salt marsh sites, displaying the importance of carefully chosen reference sites. As expected, mean values for constructed site (n = 6) and reference site (n = 11) functions were significantly different. Using constructed marsh age as the independent variable and functional indicator values as dependent variables, nonlinear regression analyses produced several ecologically meaningful trajectories (r ²> 0.9), demonstrating that the use of different‐aged marshes can be a viable approach to developing functional trajectories. The trajectories illustrated that although indicators of some functions (primary production, sediment deposition, and plant species richness) may reach natural site values relatively quickly (<10 years), others (soil organic matter content) will take longer.     

The Effect of Restoration Methods on the Quality of the Restoration and Resistance to Invasion by Exotics

The methods employed in a restoration can impact the resulting plant community. This study investigated the effect of restoration method on several indices of plant community structure by comparing two restoration methods conducted over an 8‐year period to a naturally colonized postagricultural field and a remnant grassland. The restoration methods included (1) distributing seed over fallow fields and (2) planting established seedlings in combination with seeding a fallow field. We found greater plant community resemblance (i.e., floristic quality, native species richness, and native diversity) to remnant grasslands with the introduction of seedlings during the first 4 years of restoration. There was also a negative correlation between the native plant diversity and the density of exotic plants in the restoration. This relationship suggests that introducing native plants in postagricultural fields may represent an effective management strategy to reduce exotic plant density.     

Effect of time on the natural regeneration of salt marsh

Abstract. The effect of time on natural regeneration of two salt marshes was studied in relation to plant and edaphic factors. The study was carried out in two naturally restoring salt marshes, differing in restoration time, in Txingudi (Bay of Biscay). After 20 yr, the younger salt marsh had the same plant species richness and high species similarity as a 35 yr old salt marsh (17 and 16, respectively, similarity index = 0.9), but both sites had lower species richness and similarity than a nearby natural salt marsh (36 plant species and similarity indices of 0.45 with the 35 yr old marsh and 0.46 with the 20 yr old marsh). Plant species present in the two recovering salt marshes followed a similar distribution pattern in relation to organic matter, conductivity and moisture content although this zonation differed from the natural salt marsh. The range of edaphic factors measured was also similar, but differed from those in the natural salt marsh. The process of plant species recolonization and spatial distribution might be delayed by a low probability of species arrival and by the time need for the restoration of hydrologic and edaphic factors. This study supports the necessity of long‐term monitoring in measuring coastal salt marsh restoration.     

Vegetation Monitoring of Created Dune Swale Wetlands, Vandenberg Air Force Base, California

A monitoring program was established on San Antonio Terrace at Vandenberg Air Force Base to compare vegetation development at two created wetland sites and six nearby natural wetlands. The reference wetlands were chosen to represent a range of habitats in dune swale wetlands on the Terrace. Vegetation in the reference wetland plant communities varies from low-growing herbaceous marsh species with open canopies to closed canopies dominated by shrub or tree species. Transects and plots for long-term vegetation monitoring were established in all the wetlands, stratified by plant communities in the reference wetlands and by geomorphic location in the newly created wetlands. Quantitative vegetation and environmental data were collected at all the sites; measures included species distributions, species cover, and topographical elevations. Over the first three years of monitoring, variations in groundwater depth at different geomorphic locations in the created wetlands resulted in a variety of physical conditions for plant growth. In the first year, more than 100 plant species were observed, the majority being natives. During the next two years, species richness at the created wetland sites remained relatively stable and was higher than at the reference sites. Statistical comparisons of vegetation parameters by analysis of variance and hierarchical clustering exhibited patterns of increasing similarity between the created and reference wetlands. Long-term monitoring will be continued to track the progress of vegetation at the created sites, and to assess their development relative to the reference wetlands.     

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.     

Riparian Butterfly (Papilionoidea and Hesperioidea) Assemblages Associated with Tamarix-Dominated, Native Vegetation–Dominated, and Tamarix Removal Sites along the Arkansas River, Colorado, U.S.A.

We studied butterfly assemblages at eight riparian sites over five years. Sites included Tamarix spp.–dominated riparian areas; sites where mechanical means or biological control agents (Diorhabda elongata deserticola) were used to limit Tamarix; sites that were mixtures of native woody vegetation (e.g., Populus and Salix) and Tamarix; and native vegetation sites. We identified a gradient in butterfly community composition that changed from treated Tamarix sites, through mixed vegetation, to native vegetation sites. Tamarix sites had lower butterfly metric (riparian butterfly index [RBI]) values than did native vegetation sites. The RBI is based on a combination of richness measures and the presence of specific species and groups of butterflies. There was no significant change in the RBI over sampling periods at any sites, including both Tamarix eradication sites. The RBI at sites where Tamarix control took place did not approach restoration goals based on values at unimpacted sites. Positive effects on riparian butterfly assemblages were not linked to any Tamarix control efforts, nor did we detect a decline from initial butterfly metrics at Tamarix sites. Direct ordination provided information on environmental variables, such as amount of nectar and herbaceous plant richness, which may be important in riparian restoration efforts.     

Longitudinal evaluation of vegetation richness and cover at wetland compensation sites: implications for regulatory monitoring under the Clean Water Act

There has been regulatory concern over the appropriate length of time to monitor wetland sites restored or created as compensation for impacts permitted by a U.S. Clean Water Act permit. However there is very little longitudinal research on wetland compensation sites, and conclusions on compensation site development are usually drawn from the analysis of a chronosequence of sites of different ages. This approach has limitations, given the extent of changes in wetland compensation practices and performance standards over the past few decades. In this study we conducted vegetation surveys of 22 wetland compensation sites in a rapidly developing part of the Minneapolis-St. Paul metropolitan area in 1997 and 2010. We present data on changes over time in floristic richness and cover at the site level and at the level of wetland community type within each site. Our findings do not support the assumption that wetland compensation sites progress on a trajectory toward increasing diversity, floristic quality, or native cover over time. We find that, when data from all sites are considered together, emergent communities have suffered significant declines in both floristic quality and native plant cover, while wet meadow communities have gained species richness but not species diversity. There is some evidence that site richness and cover characteristics are converging toward a regional mean over time, as the species composition of wet meadows became significantly more similar over the survey period, and all community types have significant increases in woody cover. Our study suggests the importance of selecting appropriate compensation sites that avoid foreseeable hydrologic stresses, and does not support the position that 5 years of monitoring can assure the ongoing biotic integrity of wetland compensation sites.     

Using the floristic quality concept to assess created and natural wetlands: Ecological and management implications

We applied the floristic quality index (FQI) to vegetation data collected across a chronosequence of created wetland (CW) sites in Virginia ranging in age from one to 15 years post-construction. At each site, we also applied FQI to a nearby forested reference wetland (REF). We tested the performance of the index against a selection of community metrics (species richness, diversity, evenness, percent native species) and site attributes (age, soil physiochemical variables). FQI performed better when non-native species (C-value = 0) were removed from the index, and also when calculated within rather than across vegetation layers. A modified, abundance-weighted FQI showed significant correlation with community and environmental variables in the CW herbaceous layer and REF herbaceous and shrub-sapling layers based on Canonical correspondence analysis (CCA) ordination output. These results suggest that a “natives only”, layer-based version of the index is most appropriate for our region, and an abundance-weighted FQI may be useful for assessing floristic quality in certain layers. The abundance-weighted format has the advantage of preserving the “heritage” aspect of the species conservatism concept while also entraining the “ecology” aspect of site assessment based on relative abundances of the inhabiting species. FQI did not successfully relate CW sites to REF sites, bringing into question the applicability of the FQI concept in comparing created wetlands to reference wetlands, and by analogy, the use of forested reference wetlands in general to assess vegetation development in created sites.     

Long‐term effects of prairie restoration on plant community structure and native population dynamics

The key to restoring degraded grassland habitats is identifying feasible and effective techniques to reduce the negative impacts of exotic species and promote self‐sustaining native populations. It is often difficult to extend monitoring of restoration efforts to evaluate long‐term success, but doing so is essential to understanding how initial outcomes change over time. To assess how initial treatment effects persist, we revisited degraded patches of Pacific Northwest prairie habitat 6 years after experimental restoration efforts ceased. We evaluated plant community composition to determine the lasting effects of supplemental native seeding and disturbance treatments (burning, mowing, and herbicide to reduce exotic species). We tracked the persistence of seeded species and measured spread of their populations to evaluate suitability of species for restoration and the ability of the habitat to support native plant populations. We found that plots that received supplemental seeding continued to exhibit higher richness of native species than those left unseeded, and that both seeding and disturbance treatments could positively influence native species abundance over the long term. The initially observed effects of disturbance treatments on reducing exotic grass abundance had diminished, highlighting the importance of long‐term monitoring and ongoing control of exotic species. Nevertheless, these treatments significantly influenced the population trajectories of 4 out of 8 seeded native species. There was evidence of spatial advance of most seeded species. Results from extended monitoring confirm that dispersal limitation of native species and difficulties maintaining the reduction of exotic grasses continue to be major barriers to success in restoration of invaded grasslands.     

Comparison of created and natural freshwater emergent wetlands in Connecticut (USA)

Five three- to four-year old created palustrine/emergent wetland sites were compared with five nearby natural wetlands of comparable size and type. Hydrologic, soil and vegetation data were compiled over a nearly two-year period (1988-90). Created sites, which were located along major highways, exhibited more open water, greater water depth, and greater fluctuation in water depth than natural wetlands. Typical wetland soils exhibiting mottling and organic accumulation were wanting in created sites as compared with natural sites. Typha latifolia (common cattail) was the characteristic emergent vegetation at created sites, whereas a more diverse mosaic of emergent wetland species was often associated with Typha at the natural sites. Species richness was slightly higher in created (22–45) vs. natural (20–39) wetlands, but the mean difference (33 vs. 30) was not significant. Nearly half (44%) of the 54 wetland taxa found at the various study sites were more frequently recorded at created than natural wetlands. The presence of mycorrhizae in roots of Typha angustifolia (narrow-leaved cattail) and Phragmites australis (common reed) was greater at created than natural wetlands, which may be related to differential nutrient availability. Wildlife use at all sites ranged from occasional to rare, with more sightings of different species in the natural (39) than created (29) wetlands. The presence of P. australis and introduced Lythrum salicaria (purple loosestrife) may pose a threat to future species richness at the created sites. One created site has permanent flow-through hydrology, and its vegetation and wildlife somewhat mimic a natural wetland; however, the presence of P. australis and its potential spread pose an uncertain future for this site. This study suggests the possibility of creating small palustrine/emergent wetlands having certain functions associated with natural wetlands, such as flood water storage, sediment accretion and wildlife habitat. It is premature to evaluate fully the outcome of these wetland creation efforts. A decade or more is needed, emphasizing the importance of long term monitoring and the need to establish demonstration areas.     

Native and invasive plant interactions in wetlands and the minimal role of invasiveness

The effects of invasive plants on plants native to areas that are being invaded can be quite variable, depending on the species of the invasive plant involved as well as the physical characteristics of the location being invaded. My study focuses on the effects of Phragmites australis Linnaeus (common reed) and Lythrum salicaria L. (purple loosestrife) on the same native plant community. Uninvaded plots dominated by native plants Typha angustifolia L. (narrowleaf cattail) and Typha latifolia L. (broadleaf cattail) served as the control. I surveyed percent cover of species during early summer and midsummer for 3 years in six Hudson River freshwater tidal wetlands (sites). Differences in species richness, composition and abundance were small, but significant among invaded and uninvaded plots and among sites. However, these differences remained significant when data for dominant species (invasive and native) were removed. Differences in native plant species abundance were attributed to invasive plant species-specific characteristics and differences in species richness and composition were attributed to physical location (zonation) in these freshwater tidal marshes. “Invasive” status of a dominant plant species was less important in invasive plant–native plant interactions than species-specific characteristics and zonation. Further research into the effects of site and land-use on invasive plant impacts is recommended.     

Local and landscape correlates of non‐native species invasion in restored wetlands

Vulnerability of natural communities to invasion by non‐native plants has been linked to factors such as recent disturbance and high resource availability, suggesting that recently restored habitats may be especially invasible. Because non‐native plants can interfere with restoration goals, monitoring programs should anticipate which sites are most susceptible to invasion and which species are likely to become problematic at a site. Restored sites of larger area and those with high rates of propagule input should have higher species richness of both natives and non‐natives, leading to a positive correlation between the two. However, in restored wetlands, urbanization, riparian landscape settings, and nitrogen enrichment likely favor non‐native relative to native species. We sampled 28 restored wetlands in Illinois, USA, modeled the responses of native richness, non‐native richness and non‐native cover to local and landscape predictors with linear regression, and modeled the presence/absence of 21 non‐native species with logistic regressions. Unexpectedly, native and non‐native richness were uncorrelated, suggesting different responses to environmental factors. Native richness declined with increasing available soil nitrogen and urbanization in the surrounding landscape. Non‐native richness, the richness of non‐natives relative to natives, and the likelihood of invasion by several individual invasive species decreased with increasing distance from the city of Chicago, likely in response to decreasing non‐native propagule pressure. Total cover of non‐natives, however, as well as cover by non‐native Phalaris arundinacea, increased with nitrogen availability. Our results indicate that although non‐native richness was better predicted by factors related to propagule pressure, non‐native species dominance was more closely related to local abiotic factors. Non‐native richness in restoration sites may be beyond the control of restoration practitioners, and furthermore, may be of limited relevance for conservation goals. In contrast, limiting the relative dominance of non‐natives should be a restoration priority and may be achievable through management of nutrient availability.     

Waterbird Response to Wetlands Restored Through the Conservation Reserve Enhancement Program

Abstract: Conservation programs that facilitate restoration of natural areas on private land are one of the best strategies for recovery of valuable wetland acreage in critical ecoregions of the United States. Wetlands enrolled in the Conservation Reserve Enhancement Program (CREP) provide many ecological functions but may be particularly important as habitat for migrant and resident waterbirds; however, use of, and factors associated with use of, CREP wetlands as stopover and breeding sites have not been evaluated. We surveyed a random sample of CREP wetlands in the Illinois River watershed in 2004 and 2005 to quantify use of restored wetlands by spring migrating and breeding waterbirds. Waterbirds used 75% of wetlands during spring migration. Total use-day abundance for the entire spring migration ranged from 0 to 49,633 per wetland and averaged 6,437 ± 1,887 (SE). Semipermanent wetlands supported the greatest total number of use-days and the greatest number of use-days relative to wetland area. Species richness ranged from 0 to 42 (x̄ = 10.0 ± 1.5 [SE]), and 5 of these species were classified as endangered in Illinois. Density of waterfowl breeding pairs ranged from 0.0 pairs/ha to 16.6 pairs/ha (x̄ = 1.9 ± 0.5 [SE] pairs/ha), and 16 species of wetland birds were identified as local breeders. Density of waterfowl broods ranged from 0.0 broods/ha to 3.6 broods/ha and averaged 0.5 ± 0.1 (SE) broods/ha. We also modeled spring stopover use, waterbird species richness, and waterfowl reproduction in relation to spatial, physical, and floristic characteristics of CREP wetlands. The best approximating models to explain variation in all 3 dependent variables included only the covariate accounting for level of hydrologic management (i.e., none, passive, or active). Active management was associated with 858% greater use-days during spring than sites with only passive water management. Sites where hydrology was passively managed also averaged 402% greater species richness than sites where no hydrologic management was possible. Density of waterfowl broods was 120% greater on passively managed sites than on sites without water management but was 29% less on sites with active compared to passive hydrologic management. Densities of waterfowl broods also were greatest when ratios of open water to cover were 70:30. Models that accounted for vegetation quality and landscape variables ranked lower than models based solely on hydrologic management or vegetation cover in all candidate sets. Although placement and clustering of sites may be critical for maintaining populations of some wetland bird species, these factors appeared to be less important for attracting migrant waterbirds in our study area. In the context of restored CREP wetlands, we suggest the greatest gains in waterbird use and reproduction may be accomplished by emphasizing site-specific restoration efforts related to hydrology and floristic structure. (JOURNAL OF WILDLIFE MANAGEMENT 72(3):654–664; 2008)