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.     

Testing a Passive Revegetation Approach for Restoring Coastal Plain Depression Wetlands

Restoration of coastal plain depressions, a biologically significant and threatened wetland type of the southeastern United States, has received little systematic research. Within the context of an experimental project designed to evaluate several restoration approaches, we tested whether successful revegetation can be achieved by passive methods (recruitment from seed banks or seed dispersal) that allow for wetland "self-design" in response to hydrologic recovery. For 16 forested depressions that historically had been drained and altered, drainage ditches were plugged to reestablish natural ponding regimes, and the successional forest was harvested to open the sites and promote establishment of emergent wetland vegetation. We sampled seed bank and vegetation composition 1 year before restoration and monitored vegetation response for 3 years after. Following forest removal and ditch plugging, the restored wetlands quickly developed a dense cover of herbaceous plant species, of which roughly half were wetland species. Seed banks were a major source of wetland species for early revegetation. However, hydrologic recovery was slowed by a prolonged drought, which allowed nonwetland plant species to establish from seed banks and dispersal or to regrow after site harvest. Some nonwetland species were later suppressed by ponded conditions in the third year, but resprouting woody plants persisted and could alter the future trajectory of revegetation. Some characteristic wetland species were largely absent in the restored sites, indicating that passive methods may not fully replicate the composition of reference systems. Passive revegetation was partially successful, but regional droughts present inherent challenges to restoring depressional wetlands whose hydrologic regimes are strongly controlled by rainfall variability.     

Bee Preference for Native versus Exotic Plants in Restored Agricultural Hedgerows

Habitat restoration to promote wild pollinator populations is becoming increasingly common in agricultural lands. Yet, little is known about how wild bees, globally the most important wild pollinators, use resources in restored habitats. We compared bee use of native and exotic plants in two types of restored native plant hedgerows: mature hedgerows (>10 years from establishment) designed for natural enemy enhancement and new hedgerows (≤2 years from establishment) designed to enhance bee populations. Bees were collected from flowers using timed aerial netting and flowering plant cover was estimated by species using cover classes. At mature hedgerow sites, wild bee abundance, richness, and diversity were greater on native plants than exotic plants. At new sites, where native plants were small and had limited floral display, abundance of bees was greater on native plants than exotic plants; but, controlling for floral cover, there was no difference in bee diversity and richness between the two plant types. At both mature and new hedgerows, wild bees preferred to forage from native plants than exotic plants. Honey bees, which were from managed colonies, also preferred native plants at mature hedgerow sites but exhibited no preference at new sites. Our study shows that wild bees, and managed bees in some cases, prefer to forage on native plants in hedgerows over co‐occurring weedy, exotic plants. Semi‐quantitative ranking identified which native plants were most preferred. Hedgerow restoration with native plants may help enhance wild bee abundance and diversity, and maintain honey bee health, in agricultural areas.     

Consumers and establishment limitations contribute more than competitive interactions in sustaining dominance of the exotic herb garlic mustard in a Wisconsin, USA forest

The understory is a diverse component of temperate forest ecosystems, contributing significantly to forest ecosystem services. Despite their importance, many native understories face stresses from current and past land use, habitat fragmentation, invasive species, and overabundant herbivores. We established a four block, three factor experiment to evaluate the relative contribution of native plant establishment, competitive effects from the invasive herb garlic mustard (Alliaria petiolata), and herbivory from white-tailed deer (Odocoileus virginianus) to better understand the mechanisms promoting low native plant richness and cover and understory dominance by the biennial exotic herb garlic mustard in a NE Wisconsin, USA forest. Four years of garlic mustard removal failed to increase native plant richness or cover in non-restored plots. However, deer access and the introduction of native plants (restoration treatment) both significantly enhanced native plant cover and richness, with restored species cover in fenced plots approximately 216 % that of open-access plots, and the majority of these species flowered at significantly higher proportions inside of fenced areas. In contrast, deer access did not significantly alter the cover, or seed production of garlic mustard. We also found no significant effect of garlic mustard presence on the cover or flowering of restored native species. We conclude that multiple factors, including limited natural establishment by native species and selective herbivory drove low native, high exotic dominance at our site, suggesting that a shift in focus from invasive plant removal to combined native plant restoration and herbivore control is needed to maximize the recovery of this degraded forest understory.     

Predictability of flood pulse driven assembly rules for restoration of a floodplain plant community

Community assembly rules were formulated to evaluate the restoration of wet prairie along the periphery of the floodplain of the Kissimmee River in central Florida. Restoration of this plant community is expected to be driven by the reestablishment of flood pulse hydrology following the ongoing dechannelization of the river. Assembly rules were assessed with plant species composition and cover data from 15 permanent plots on the restored floodplain and 6 control plots on the channelized floodplain. These sites were sampled biannually from 1998 to 2010. Mean annual hydroperiods and depths confirmed that the frequency, duration and amplitude of post-restoration flood pulses at study sites were similar to historic reference locations. Elimination of pasture grasses (primarily Paspalum notatum Flüggé) following restoration of the flood pulse validated the hypothesized deletion rule for initial transformation of the wet prairie zone. Predicted increased dominance of obligate and facultative wetland species, a “community addition rule”, also was confirmed. An index of weighted averages of wetland indicator taxa showed significant short-term responses to antecedent hydroperiods and depths, and a restoration trajectory for wetland plant species. As predicted, recruitment of wet prairie indicator species from the extant seed bank correlated with reestablishment of the flood pulse, but was greatest when inundation extended from the wet season into the dry season. Restoration of a wetland plant community did not result in the predicted increase in species richness and diversity. Colonization and expansion of the exotic grass, Hemarthria altissima (Poir.) Stapf & C.E. Hubb., disrupted community reassembly processes. By summer 2007, mean cover of this species and several other exotic grasses increased to 24%, and necessitated herbicide treatments. Assembly rules provided useful predictions for the initial restoration of wet prairie vegetation, but were eventually confounded by the spread of an exotic species that was new to the regional flora.     

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.     

Terrestrial Arthropods as Indicators of Ecological Restoration Success in Coastal Sage Scrub (California, U.S.A.)

Abstract Ecological restoration enjoys widespread use as a technique to mitigate for environmental damage. Success of a restoration project often is evaluated on the basis of plant cover only. Recovery of a native arthropod fauna is also important to achieve conservation goals. I sampled arthropod communities by pitfall trapping in undisturbed, disturbed, and restored coastal sage scrub habitats in southern California. I evaluated arthropod community composition, diversity, and abundance using summary statistics, cluster analysis, and detrended correspondence analysis (DCA) and investigated influence of vegetation on arthropod communities with multiple regression analysis. Arthropod diversity at undisturbed and disturbed sites was greater than at sites that were 5 and 15 years following restoration ( p < 0.05). Number of arthropod species was not significantly different among undisturbed, disturbed, and restored sites, and two restoration sites had significantly more individuals than other sites. Vegetation at disturbed and undisturbed sites differed significantly; older restorations did not differ significantly from undisturbed sites in diversity, percent cover, or structural complexity. In multiple regression models, arthropod species richness and diversity was negatively related to vegetation height but positively related to structural complexity at intermediate heights. Exotic arthropod species were negatively associated with overall arthropod diversity, with abundance of the earwig Forficula auricularia best predicting diversity at comparison (not restored) sites (r² = 0.29), and abundance of the spider Dysdera crocata and the ant Linepithema humile predicting diversity at all sites combined (r² = 0.48). Native scavengers were less abundant at restored sites than all other sites and, with a notable exception, native predators were less abundant as well. DCA of all species separated restored sites from all other sites on the first axis, which was highly correlated with arthropod diversity and exotic arthropod species abundance. Lower taxonomic levels showed similar but weaker patterns, with example families not discriminating between site histories. Vegetation characteristics did not differ significantly between the newly restored site and disturbed sites, or between mature restoration sites and undisturbed sites. In contrast, arthropod communities at all restored sites were, as a group, significantly different from both disturbed and undisturbed sites. As found in other studies of other restoration sites, arthropod communities are less diverse and have altered guild structure. If restoration is to be successful as compensatory mitigation, restoration success standards must be expanded to include arthropods.     

Is fencing enough? The short‐term effects of stock exclusion in remnant grassy woodlands in southern NSW

Summary Fencing remnant native vegetation has become a widespread activity for arresting declines in biodiversity in agricultural landscapes. However, few data are available on the effectiveness of this approach. The present study investigated the short-term effects of fencing to exclude livestock on dominant tree and shrub recruitment, plant species cover, litter and soil characteristics in remnant grassy woodlands in southern NSW. Vegetation and soil surveys were undertaken at 47 sites fenced by Greening Australia (NSW) for 2–4 years. Fenced and unfenced areas at each site were compared using split-plot sampling. Woodlands sampled were dominated by Yellow Box/Blakely's Red Gum ( Eucalyptus melliodora/Eucalyptus blakelyi ), Grey Box ( Eucalyptus microcarpa ) or White Cypress-pine ( Callitris glaucophylla ). Significantly higher numbers of tree recruits were found in the fenced sites, with tree recruitment found in 59% of fenced sites compared with 13% of unfenced sites. Fenced sites also had significantly greater cover of native perennial grasses, less cover of exotic annual species and less soil surface compaction. However, outcomes varied among woodland ecosystems and individual sites. Where tree recruitment occurred, there was significantly more tree recruitment where there was greater perennial grass cover and less regeneration where exotic annual grass cover or overstorey crown cover was dense. Few shrubs recruited in fenced or unfenced areas, reflecting the lack of mature shrubs in most sites. Fencing is an important first step for conserving threatened grassy woodlands, but more active management may be needed to enhance woodland recovery, particularly in sites where few or no recruits were found.
Key words bush regeneration, fencing, grazing exclusion, rehabilitation, woodland restoration.     

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.     

Succession of Exotic and Native Species Assemblages within Restored Floodplain Forests: A Test of the Parallel Dynamics Hypothesis

Exotic plants pose a threat to restoration success in post‐agricultural bottomlands, but little information exists on their dynamics during succession of actively restored sites. We hypothesized that exotic assemblages would establish during succession and that their compositional trends during succession time would mirror those published for native species in other systems, with an early peak in herbaceous richness followed by a decline as woody species establish. In the summer of 2008, we sampled 16 sites across an 18‐year chronosequence of restored forests, with an additional four mature forest stands for comparison, within the Cypress Creek NWR, Illinois, U.S.A. We identified all vascular plant species and quantified canopy openness at three canopy strata, and soil texture and chemistry. Trends in exotic assemblages were significantly correlated with canopy openness at all strata. Richness of exotic and native herbaceous species was related to stand age and consistent with a Weibull regression model. Native and exotic herbaceous cover followed an exponential decay model. Woody native richness over time conformed to a logistic model; woody exotics exhibited no relationship with stand age and were present in sites of all ages. Our results indicate that although their rates of decline differ, herbaceous exotics and natives exhibit similar successional dynamics; therefore, herbaceous exotics may not pose a lasting threat to restoration success in reforested floodplains. Woody exotics can establish across a range of successional stages and persist under closed canopy conditions. Bottomland restorations are vulnerable to the invasion and expansion of exotic plant species even after canopy closure.     

Management of invasive plants through ecological resistance

Despite debates on the real impact of plant invasion on native biodiversity, there remain many situations where exotic invasive plants must be managed and habitats restored. Restoration practices that build on plant community assembly principles could be useful to delay or prevent re-invasion after control, but there are still few syntheses of the biodiversity theory, ecological mechanisms and experimental evidence relevant to invasive plant management, possibly delaying applications. To provide such a synthesis, we review current knowledge on three key determinants of invasion success: biotic resistance, abiotic constraints, and propagule pressure. We elaborate on the ecological mechanisms at play for each determinant and emphasize, using case studies, their relevance for invasive plant management and ecological restoration. We find evidence that restoring a plant cover can enhance invasion resistance, but the challenge for both research and field applications is to understand how multiple determinants interact in relation to species traits in the fields. Failure to recognize these interactions and their effect on community assembly processes may explain some of the mixed species responses observed. While we need control and restoration case studies with local species at different sites, the development of a coherent, dynamic and adaptive framework around biotic/ecological resistance will have to go beyond the idiosyncrasy of the many species and systems being tested. Emphasizing the functional diversity of the restored community seems a promising approach when facing potentially multiple invaders and/or fluctuating abiotic conditions.     

Riparian zones as havens for exotic plant species in the central grasslands

In the Central Grasslands of the United States, we hypothesized that riparian zones high in soil fertility would contain more exotic plant species than upland areas of low soil fertility. Our alternate hypothesis was that riparian zones high in native plant species richness and cover would monopolize available resources and resist invasion by exotic species. We gathered nested-scale vegetation data from 40 1 m²subplots (nested in four 1000 m² plots) in both riparian and upland sites at four study areas in Colorado, Wyoming, and South Dakota (a total of 320 1 m² subplots and 32 1000 m² plots). At the 1 m² scale, mean foliar cover of native species was significantly greater (P<0.001) in riparian zones (36.3% ± 1.7%) compared to upland sites (28.7% ± 1.5%), but at this small scale there were no consistent patterns of native and exotic species richness among the four management areas. Mean exotic species cover was slightly higher in upland sites compared to riparian sites (9.0% ± 3.8% versus 8.2% ± 3.0% cover). However, mean exotic species richness and cover were greater in the riparian zones than upland sites in three of four management areas. At the 1000 m² scale, mean exotic species richness was also significantly greater (P<0.05) in riparian zones (7.8 ± 1.0 species) compared to upland sites (4.8 ± 1.0 species) despite the heavy invasion of one upland site. For all 32 plots combined, 21% of the variance in exotic species richness was explained by positive relationships with soil % silt (t =1.7, P=0.09) and total foliar cover (t = 2.4, P=0.02). Likewise, 26% of the variance in exotic species cover (log₁₀ cover) was explained by positive relationships with soil % silt (t =2.3, P=0.03) and total plant species richness (t = 2.5, P=0.02). At landscape scales (four 1000 m² plots per type combined), total foliar cover was significantly and positively correlated with exotic species richness (r=0.73, P<0.05) and cover (r=0.74, P<0.05). Exotic species cover (log₁₀ cover) was positively correlated with log₁₀% N in the soil (r=0.61, P=0.11) at landscape scales. On average, we found that 85% (±5%) of the total number of exotic species in the sampling plots of a given management area could be found in riparian zones, while only 50% (±8%) were found in upland plots. We conclude that: (1) species-rich and productive riparian zones are particularly invasible in grassland ecosystems; and (2) riparian zones may act as havens, corridors, and sources of exotic plant invasions for upland sites and pose a significant challenge to land managers and conservation biologists.     

Unrealized Expectations for Restoration of a Floodplain Plant Community

The ongoing restoration of the channelized Kissimmee River is expected to promote reestablishment of the prolonged, deep inundation regimes that sustained broadleaf marsh as the dominant wetland plant community on the historical floodplain. The success of the restoration was evaluated at locations on the remnant floodplain where broadleaf marsh had been replaced by a mesophytic shrub community, and on the lower portion of the reconstructed floodplain, which was recreated by backfilling of a flood control canal and degradation of associated spoil mounds. During the 8‐year post‐restoration period (2001–2008) mean annual hydroperiods and depths on the restored floodplain were not significantly different from pre‐channelization hydrologic conditions at historical reference sites. Increased hydroperiods and depths eliminated the mesophytic shrub (primarily Myrica cerifera) and associated fern cover, and led to colonization of floating and mat‐forming species, but did not result in the reestablishment of a broadleaf marsh community. Signature broadleaf marsh species, Sagittaria lancifolia and Pontederia cordata, were found in all remnant floodplain plots and colonized 8 of the 10 reconstructed floodplain plots, but had mean cover ranging from only 0.9 to 6.1%. Several factors may have contributed to unsuccessful reestablishment of broadleaf marsh, including unfavorable edaphic conditions, brief drawdown (low stage) periods for establishment of seedlings, flood induced mortality, and an invasion of the exotic shrub, Ludwigia peruviana, which had post‐restoration mean cover of 17–19%. Study results indicate hydrologic restoration of floodplain plant communities can be influenced by more discrete aspects of the river flood pulse than average hydroperiods and depths.     

Experimental Restoration of Native Vegetation in Indiana Dunes National Lakeshore

We investigated the effects of prescribed fire, herbicide treatment, and sod removal on the eradication of exotic grasses and the establishment of native plant species in 24 experimental restoration plots in three razed residential sites within the boundary of Indiana Dunes National Lakeshore. During 1992–1995, herbicide treatment and sod removal decreased the combined cover of Poa pratensis (Kentucky blue grass) and Agropyron repens (quackgrass) significantly (from 82% to 13%, and 85% to 8%, respectively), whereas fire did not suppress such exotic lawn grasses. In 1993, several opportunistic species, represented by Cyperus spp. (umbrella sedges), Digitaria sanguinalis (crab grass), and Ambrosia artemisiifolia (common ragweed), filled the gaps left by the removal of lawn grasses. For the same period, Detrended Correspondence Analysis revealed a clear vegetation divergence between the control-fire plots and the herbicide-sod removal plots. While Poa pratensis and Agropyron repens continued to dominate the control and fire plots, the planted native species, represented by Schizachyrium scoparium (little blue-stem), Sorghastrum nutans (Indian grass), Rudbeckia hirta (black-eyed Susan), and Monarda punctata (horsemint), began to dominate in the herbicide and sod removal plots from 1994. In both herbicide and sod removal plots, the ground cover of grasses (68%) was much higher than the forbs (10%). The herbicide plots, where exotic species were removed but nitrogen-rich top soils were not removed, showed a higher diversity of planted native species than the sod removal plots (where both exotic species and top soils were removed) and the control-fire plots (where neither was removed). This finding suggests that an optimum but not excessive concentration of soil nitrogen is needed to support a maximum species diversity in such infertile substrate as sandy soil. In addition, the decrease in potassium in all plots, regardless of treatment, suggests that potassium may become a limiting factor for our restored native vegetation.     

Soil Nitrogen Conditions Approach Preinvasion Levels following Restoration of Nitrogen-Fixing Black Locust (Robinia pseudoacacia) Stands in a Pine–Oak Ecosystem

Restoring native plant communities on sites formerly occupied by invasive nitrogen‐fixing species poses unique problems due to elevated soil nitrogen availability. Mitigation practices that reduce available nitrogen may ameliorate this problem. We evaluated the effects of tree removal followed by soil preparation or mulching on native plant growth and soil nitrogen transformations in a pine–oak system formerly occupied by exotic nitrogen‐fixing Black locust (Robinia pseudoacacia) trees. Greenhouse growth experiments with native grasses, Andropogon gerardii and Sorghastrum nutans, showed elevated relative growth rates in soils from Black locust compared with pine–oak stands. Field soil nutrient concentrations and rates of net nitrification and total net N‐mineralization were compared 2 and 4 years since Black locust removal and in control sites. Although soil nitrogen concentrations and total net N‐mineralization rates in the restored sites were reduced to levels that were similar to paired pine–oak stands after only 2 years, net nitrification rates remained 3–34 times higher in the restored sites. Other nutrient ion concentrations (Ca, Mg) and organic matter content were reduced, whereas phosphorus levels remained elevated in restored sites. Thus, 2–4 years following Black locust tree removal and soil horizon mixing achieved through site preparation, the concentrations of many soil nutrients returned to preinvasion levels. However, net nitrification rates remained elevated; cover cropping or carbon addition during restoration of sites invaded by nitrogen fixers could increase nitrogen immobilization and/or reduce nitrate availability, making sites more amenable to native plant establishment.     

Disturbance is more important than seeding or grazing in determining soil microbial communities in a semiarid grassland

A primary goal of ecological restoration is often to return processes and functions to degraded ecosystems. Soil, while often ignored in restoration, supports diverse communities of organisms and is a fundamental actor in providing ecosystem processes and services. We investigated the impact of seeding and livestock grazing on plant communities, soil microorganisms, and soil fertility 3 years after the restoration of a disturbed pipeline corridor in southeastern Arizona. The initial soil disturbance and topsoil treatment, regardless of seeding or grazing, was the most influential factor in determining differences in both plant and microbial communities. Compared with the control, the disturbed and restored sites had greater plant species richness, greater total herbaceous plant cover, greater soil organic matter, higher pH, and differed in soil nutrients. Bacteria and fungi appeared to generally correlate with micro‐environment and soil physiochemical properties rather than specific plant species. The undisturbed control had a smaller proportion of bacterial functional groups associated with the breakdown of plant biomass (polysaccharide decomposition) and a smaller proportion of arbuscular mycorrhizal fungi (AMF) compared with disturbed and restored sites. The ability of the unseeded disturbed site to recover robust vegetation may be due in part to the high presence of AMF. These differences show selection for soil microorganisms that thrive in disturbed and restored sites and may contribute to increased plant productivity. Restoration of specific plant species or ecological processes and services would both benefit from better understanding of the impacts of disturbance on soil microorganisms and soil fertility.     

Effects of Stream Restoration on Woody Riparian Vegetation of Southern Appalachian Mountain Streams,North Carolina,U.S.A

Riparian revegetation, such as planting woody seedlings or live stakes, is a nearly ubiquitous component of stream restoration projects in the United States. Though evaluations of restoration success usually focus on in‐stream ecosystems, in order to understand the full impacts of restoration the effects on riparian ecosystems themselves must be considered. We examined the effects of stream restoration revegetation measures on riparian ecosystems of headwater mountain streams in forested watersheds by comparing riparian vegetation structure and composition at reference, restored, and degraded sites on nine streams. According to mixed model analysis of variance (ANOVA), there was a significant effect of site treatment on riparian species richness, basal area, and canopy cover, but no effect on stem density. Vegetation characteristics at restored sites differed from those of reference sites according to all metrics (i.e. basal area, canopy cover, and species composition) except species richness and stem density. Restored and degraded sites were structurally similar, with some overlap in species composition. Restored sites were dominated by Salix sericea and Cornus amomum (species commonly planted for revegetation) and a suite of disturbance‐adapted species also dominant at degraded sites. Differences between reference and restored sites might be due to the young age of restored sites (average 4 years since restoration), to reassembly of degraded site species composition at restored sites, or to the creation of a novel anthropogenic ecosystem on these headwater streams. Additional research is needed to determine if this anthropogenic riparian community type persists as a resilient novel ecosystem and provides valued riparian functions.     

Identifying Native Vegetation for Reducing Exotic Species during the Restoration of Desert Ecosystems

There is currently much interest in restoration ecology in identifying native vegetation that can decrease the invasibility by exotic species of environments undergoing restoration. However, uncertainty remains about restoration's ability to limit exotic species, particularly in deserts where facilitative interactions between plants are prevalent. Using candidate native species for restoration in the Mojave Desert of the southwestern U.S.A., we experimentally assembled a range of plant communities from early successional forbs to late‐successional shrubs and assessed which vegetation types reduced the establishment of the priority invasive annuals Bromus rubens (red brome) and Schismus spp. (Mediterranean grass) in control and N‐enriched soils. Compared to early successional grass and shrub and late‐successional shrub communities, an early forb community best resisted invasion, reducing exotic species biomass by 88% (N added) and 97% (no N added) relative to controls (no native plants). In native species monocultures, Sphaeralcea ambigua (desert globemallow), an early successional forb, was the least invasible, reducing exotic biomass by 91%. However, the least‐invaded vegetation types did not reduce soil N or P relative to other vegetation types nor was native plant cover linked to invasibility, suggesting that other traits influenced native‐exotic species interactions. This study provides experimental field evidence that native vegetation types exist that may reduce exotic grass establishment in the Mojave Desert, and that these candidates for restoration are not necessarily late‐successional communities. More generally, results indicate the importance of careful native species selection when exotic species invasions must be constrained for restoration to be successful.     

Savannas after afforestation: Assessment of herbaceous community responses to wildfire versus native tree planting

Afforestation and fire exclusion are pervasive threats to tropical savannas. In Brazil, laws limiting prescribed burning hinder the study of fire in the restoration of Cerrado plant communities. We took advantage of a 2017 wildfire to evaluate the potential for tree cutting and fire to promote the passive restoration of savanna herbaceous plant communities after destruction by exotic tree plantations. We sampled a burned pine plantation (Burned Plantation); a former plantation that was harvested and burned (Harvested & Burned); an unburned former plantation that was harvested, planted with native trees, and treated with herbicide to control invasive grasses (Native Tree Planting); and two old-growth savannas which served as reference communities. Our results confirm that herbaceous plant communities on post-afforestation sites are very different from old-growth savannas. Among post-afforestation sites, Harvested & Burned herbaceous communities were modestly more similar in composition to old-growth savannas, had slightly higher richness of savanna plants (3.8 species per 50-m²), and supported the greatest cover of native herbaceous plants (56%). These positive trends in herbaceous community recovery would be missed in assessments of tree cover: whereas canopy cover in the Harvested & Burned site was 6% (less than typical of savannas of the Cerrado), the Burned Plantation and Native Tree Planting supported 34% and 19% cover, respectively. By focusing on savanna herbaceous plants, these results highlight that tree cutting and fire, not simply tree planting and fire exclusion, should receive greater attention in efforts to restore savannas of the Cerrado.