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Article

Effects of Non-Native Annual Plant Removal on Native Species in Mediterranean-Climate Shrub Communities

1
Center for Environmental Biology, University of California, Irvine, CA 92697-2525, USA
2
Department of Ecology & Evolutionary Biology, University of California, Irvine, CA 92697-2525, USA
3
Irvine Ranch Conservancy, 4727 Portola Parkway, Irvine, CA 92620-1914, USA
*
Author to whom correspondence should be addressed.
Diversity 2024, 16(2), 115; https://doi.org/10.3390/d16020115
Submission received: 5 January 2024 / Revised: 3 February 2024 / Accepted: 6 February 2024 / Published: 9 February 2024
(This article belongs to the Section Biodiversity Conservation)

Abstract

:
Removal of non-native plants is known to increase overall native cover within degraded communities that contain at least a small percentage of native plant cover. We investigated the mechanisms behind this pattern, asking whether removal of non-native annual species increases the density and species richness of the native community through increased seedling recruitment or through the growth of established native shrubs. We also investigated whether the effectiveness of non-native removal was influenced by region (coastal versus inland) and whether there was a threshold of native cover required for invasive removal to be effective. We established 13 study sites (7 coastal and 6 inland) located throughout the Nature Reserve of Orange County, CA, USA. Each degraded site contained four paired plots corresponding to a range of existing native plant cover: low 20–29%, medium-low 30–39%, medium-high 40–49%, and high cover 50–59% with one plot per pair subjected to non-native removal. We collected plant density, species richness, and established native shrub volume measurements to clarify the effectiveness of non-native removal. Non-native plant removal reduced non-native annual recruitment, increased that of native shrub seedlings, but had no impact on native forb recruitment. Non-native removal increased the number and reduced mortality of established native shrubs but did not influence shrub size. Native seedling density, species richness, and established native shrub number were highest inland, but coastal sites had larger adult shrubs. We found that non-native removal was most effective for increasing native density and species richness for degraded inland sites with less than 40% of existing native cover. The initial native cover did not affect established shrub volume or number. Our results confirm the importance of non-native plant removal in areas with medium-low or low native cover to increase native recruitment, species richness, adult shrub number, and to reduce established shrub mortality, especially during extreme drought.

1. Introduction

The Mediterranean biome, which supports high levels of endemism and plant biodiversity, has experienced great loss of biodiversity primarily due to climate and land use change [1,2,3]. Anthropogenic impacts, such as land development, increased fire frequency, nitrogen deposition, climate-change induced drought, and over a century of intensive grazing, threaten plant communities around the globe and have resulted in an increase in the cover of non-native species. In our coastal sage scrub system, this has led to a conversion of native shrublands into non-native annual grasslands [4,5,6]. Healthy coastal sage scrub primarily consists of drought-deciduous shrubs with a diverse native herbaceous understory, yet most coastal sage scrub communities have been invaded by non-native annual grasses and forbs, leading to a hybrid non-native grass–native shrub community. Non-native annuals are not necessarily harmful to an undisturbed, well-established shrub community, but when combined with disturbances, such as prologued drought and increasingly frequent wildfires, they can be highly invasive, eventually leading to vegetation-type conversion from a perennial native shrub-dominated community to an invasive annual community [5,6]. Land stewards have tested multiple ecological restoration methods to reverse the effects of degradation and return annual non-native grass-dominated landscapes to native shrubs [7,8].
Restoration efforts often focus on removal of the non-native annuals, either by hand weeding or herbicide application. When vegetation type-conversion from native shrubland to a non-native annual community has already occurred, such as in the case of heavily degraded communities where key ecosystem processes are altered, more robust active techniques involving the addition of native plants, seeds, or even soil is necessary [9,10,11]. At lower levels of non-native cover, if important ecosystem processes have not yet been impacted and there is a remnant intact native plant community, then non-native removal alone would be just as effective and even preferred [4,7,11,12,13]. Non-natives may not be a threat to the native community without additional disturbance, and removal efforts can result in the accidental removal of natives [14]. At some threshold level of native cover, non-native removal may allow the native community to naturally regenerate following the removal of the physical disturbance. Although adding natives to the landscape is sometimes necessary for restoration, non-native removal alone can be less labor-intensive and more cost-effective [15,16,17,18]. Land managers frequently spend a large part of their budget on non-native removal [8], yet the underlying mechanisms and site conditions that allow for the success of this approach are not quantified.
In disturbed areas, non-native annual plants can germinate quickly and competitively exclude native plants from fundamental resources, such as light, nutrients, space, and water [12,19,20,21,22,23]. Ultimately, insufficient access to resources due to competition can reduce native cover, growth, and species richness [19,20,23,24]. In Southern California, non-native annuals are expected to compete more with native shrubs during the seedling establishment phase when they are accessing resources from the same top few centimeters of soil. Non-native annuals leave behind a dense layer of litter and thatch that can reduce the germination of native plants [25,26,27]. Once their deep roots are established, native shrubs are better able to compete with non-native annuals [7]. Therefore, the removal of non-native species followed by natural regeneration of the native shrub community should reverse the competitive effects of non-native annuals. In fact, several studies have shown that non-native removal successfully increased native cover, density, growth, and species richness, and improved access to light and soil nutrients [28,29]. Removing one non-native can lead to an increase in another non-native, pointing to the importance of evaluating site conditions best suited to non-native removal without active restoration [30,31].
Due to differences in environmental conditions, such as moisture availability and temperature, abundance of non-native species and restoration success may vary between regions [32,33]. Sites located further from the coast experience warmer summer temperatures and greater evapotranspirative stress, which impacts plant species richness and composition [32]. Higher resource environments tend to be more heavily invaded, as most non-natives are fast-growing and able to quickly take advantage of available resources [34,35,36]. However, non-native species also successfully invade low-resource environments, possibly due to greater efficiency of resource use [37,38]. The native herbaceous annuals (forbs) that comprise the understory of a healthy coastal sage scrub community germinate more in wet years, so regional differences may also influence native species richness by altering the density and diversity of native annuals [39]. This may impact non-native density as well, as diverse native communities are typically more resistant to invasion [40].
Theoretical work suggests that thresholds of resilience may facilitate recovery at sites with high native cover, while heavily degraded areas may not recover [11,41,42]. The existing vegetation cover predicts the species composition of the seed dispersed and vegetation cover presented in the following year [43,44]. Limited native seed rain and profuse non-native seed production, also known as “seed swamping”, hinders native recovery [43,45,46]. Areas with high non-native cover often see a reduction in native cover, with sites containing a level of non-native cover exceeding a threshold experiencing greater difficulty with native recovery [24]. In such heavily degraded areas, removing one non-native species without adding natives will typically lead to the invasion of a different non-native species [17]. Less studied is whether there is a management threshold of native cover required for non-native removal without the addition of native plants to be successful.
Previous work at our study site demonstrated that non-native plant removal resulted in higher native cover in weeded plots [47]. In this study, we examined the possible mechanisms and identified necessary site conditions for this result by investigating the relative role of native shrub and forb seedling recruitment versus growth from mature shrubs in areas with varying initial native cover. Specifically, we asked the following: (1) Does non-native plant removal increase native cover through increased seedling recruitment or by promoting the growth of established native shrubs? We hypothesized that removal of non-natives would promote seedling recruitment of native shrubs and forbs by decreasing competition for water and other resources [7,48]. In contrast, we hypothesized that growth of existing shrubs would not be influenced by non-native removal because the perennial natives access deeper water than that used by non-native annuals [49,50]. (2) Does the success of non-native removal vary depending on site conditions? We hypothesized that non-native removal would vary from the coast to inland sites, along with variation in environmental conditions including temperatures, soil nutrients, and soil water-holding capacity [32]. We also hypothesized that we would identify a threshold of initial native cover at which non-native removal was no longer effective [51]. Ultimately, the results of this study reveal the mechanisms by which non-native removal increases native cover and clarify the ideal site conditions for which this technique is most effective.

2. Materials and Methods

We established thirteen restoration sites throughout the Nature Reserve of Orange County, California, with ten established in 2010 and three added in 2014 (Figure 1). All 13 study sites were located within Irvine Ranch Natural Landmarks with 6 sites in the inland region and 7 sites in the coastal portion (Figure 1). Study sites were located within invaded areas of coastal sage scrub plant communities ranging in levels of remaining native cover and shared dominant species typical of this community, such as Artemisia californica, Eriogonum fasciculatum, and Salvia mellifera [52]. Non-native species included Bromus diandrus, B. madritensis, Avena barbata, A. fatua, Erodium cicutarium, Brassica nigra, Hirschfeldia incana, and Centauria melitensis. These are all commonly found within disturbed coastal sage scrub communities and are known to vary in terms of their environmental impact [53,54]. For example, Brassica nigra and Hirschfeldia incana are known to release allelopathic chemicals, reducing soil microbe abundance and leaving lasting impacts [55,56]. Erodium cicutarium and Bromus madritensis are commonly found even in native-dominated California plant communities and only displace native shrubs when combined with disturbances, such as drought or increases in fire frequency [57].
Degradation of this plant community in this region is the result of physical disturbance from decades of overgrazing in combination with drought, urban development, and fire, which facilitated invasion by non-native annual grasses and forbs [4,58]. Restoration sites were located on soils ranging from clay loams to sandy loams (Table A1; [59]). Although there was some variation in soil type, slope, and aspect between sites and region, the variation was within the range expected by this habitat type [60]. The climate is Mediterranean, characterized by mild, wet winters and hot, dry summers. The mean annual precipitation is 32.3 cm (1987–2018 weather, Tustin Irvine Ranch Station, NCDC #9087, 33°44′ N, 117°47′ W, elevation 36 m) with rain falling predominantly from November to April.
We selected sites in areas consisting of coastal sage scrub using available digital vegetation maps for the regions [61]. Site selection was finalized after ground-based reconnaissance of candidate locations to ensure they met the criteria for co-dominant species and a range of native shrub cover invaded by non-native annuals (Figure 2). Although native grasses and forbs were also present at the site, the proportion of total vegetation cover that both growth forms occupied were negligible compared to that of native shrubs. Given our interest in identifying thresholds of native cover that optimizes non-native removal, we established four initial native plant cover classes, namely (1) 20–29% low, (2) 30–39% medium-low, (3) 40–49% medium-high, and (4) 50–59% high cover, based on visual estimates. The remaining cover was a mixture of non-native species, bare ground, and negligible amounts of native annuals. Overall plant cover was determined from visual estimates of species-by-species cover taken from the entire plot, validated with point-intercept estimates subsampled within Griffoul 2017. For each cover class, two 5 m × 5 m plots were established within 10 m of each other. Of these two plots, one plot was randomly assigned to the non-native weed removal treatment while the other became the unmanipulated control. This resulted in a total of 8 experimental plots at each site, with each plot representing a unique native cover class and weed treatment combination. In 2014, we installed a smaller 0.5 m × 0.5 m subplot in a random, open portion of the 5 m × 5 m plot to obtain representative assessments of native seedling recruitment.
We started removing non-native species at the initiation of the study in 2010. At the beginning of each growing season, we applied low-dose glyphosate, a broad-spectrum herbicide, at 0.5 qts/ac (1.2 L/ha) for a 0.5% concentration of Roundup PROMAX® using a backpack sprayer to favor native germination by eliminating non-native species that sprouted after the winter rains. The start of each growing season was marked by the first germinating rain events of the year that typically occur around January. In situations where non-natives were too interspersed with native species for us to safely spot-treat with herbicide, we waited until later in the season to remove the non-natives by hand. Every May, we mechanically removed non-native plants by hand or with weed-eaters to further reduce competition and the quantity of non-native seed entering the seed bank. We implemented the weed removal treatment within a 7 × 7 m area (5 × 5 m plot with 1 m extensions). Non-native removal was conducted within each weed-treated plot, specifically targeting areas densely covered with non-natives to mimic actual weeding methods used in local large-scale restoration projects that reduce non-natives without removing every single non-native plant. Litter and thatch were not intentionally removed along with the non-natives, although weeded plots did have a significantly greater cover of bare ground compared to control plots across all years (F1,252 = 18.92, p = 0.0001).
Every year, from 2014 to 2016, we collected plant density measurements at all thirteen restoration sites to study how non-native removal impacted seedling recruitment throughout the growing season. Near the beginning of each growing season, in January, all native and non-native seedlings were identified and counted within the smaller 0.5 × 0.5 m subplots. We defined seedlings as young plants that have germinated and emerged following the first winter rain event of the year. In May, we recorded the density of native and non-native individuals still present in our subplot towards the end of the growing season.
To evaluate how non-native plant removal affected established shrub growth, we measured and calculated the volume of all native shrubs taller than 1 m within each experimental plot in fall 2012, towards the beginning of the recent severe drought in California, and again in Spring 2014, the peak year of the drought. During fall 2012, we only collected data at the ten restoration sites that were established in 2010 and which had already received two full years of weed removal. We did not sample the three restoration sites (Cut Across, Moro Ridge, and Gypsum) that were added in 2014. During spring 2014, we collected shrub data at all thirteen restoration sites. Size measurements, taken at the base of the shrub, included height (H), length at the widest point (L), and width at a 90º angle from the widest point (W). Shrub volume, assumed to be cylindrical, was calculated using the formula Vshrub = π × ((W + L)/4)2 × H. The average shrub volume, total shrub volume, and number of shrubs were calculated for each plot and year of measurement. In 2014, many dead shrubs were observed in our plots, so the number of dead shrubs was also recorded.
To evaluate the effect of non-native plant removal on native and non-native plant density and species richness over the course of three years (2014–2016) for winter and spring, we performed repeated measures mixed model ANOVAs followed by Tukey–Kramer post hoc tests using the PROC MIXED SAS 9.4 software [62]. Plot was included in the model as the repeated factor (measured in multiple years) while treatment (control or weeded), initial native cover (low, medium-low, medium-high, or high), and region (coastal or inland) were fixed factors. Site (the thirteen study locations, an experimental blocking unit containing all treatment combinations) was included as a random factor in our analyses. Plant density data were log-transformed (ln(x + 1)) while species richness data were square-root-transformed (sqrt(x + 1)) to satisfy ANOVA’s requirement for normality. We performed these analyses on the total density of native, native shrub, native forb, and non-native seedlings, and on native and non-native species richness.
To study the effect of non-native removal on already-established native shrubs, we again used repeated measures mixed model ANOVAs to compare differences in the average volume per plot, total volume per plot, and the number of living native shrubs at the ten restoration sites originally established in 2010. We used the same model described above (treatment, initial native cover, and region as fixed factors, site as a random factor, and plot as the repeated factor) to analyze shrub size and number. We excluded the three sites (Cut Across, Moro Ridge, and Gypsum) that were established in 2014 because shrub size data was only collected once in 2014. Average shrub volume and number were both ln-transformed to fit a normal distribution. We used PROC GLIMMIX to conduct a logistic regression with site as a random variable and treatment, region, and cover as fixed factors, to determine whether the proportion of dead native shrubs observed in 2014 was related to treatment, initial native cover, or region.

3. Results

Non-native removal had mixed effects on native coastal sage scrub seedling recruitment. Although non-native removal did not increase the density of native seedlings that germinated in the winter, native density was significantly higher in weeded plots in the spring (Table 1 and Table A2, Figure 3a). When evaluating the composition of the native seedlings based on functional group, we found that shrub seedlings were significantly more abundant in weeded compared to control plots in winter and spring, while herbaceous forb species were not influenced by non-native removal in either season (Table 1 and Table A2, Figure 3b,c). Non-native removal significantly reduced non-native seedling recruitment, with the density of non-natives germinating in the winter and present in the spring consistently lower in weeded plots (Table 1 and Table A2, Figure 3d).
Weeded plots with the two lowest initial cover classes (20–29% low and 30–39% medium-low) contained significantly higher native seedling density compared to control plots with the same level of initial cover, suggesting that non-native removal is most effective in areas with an initial native cover of 20–39% (Table 1 and Table A2). The initial native plant cover did not significantly impact native shrub and forb density (Table 1) but did influence non-native seedling density in the spring (Table 1). Non-native density was greatest in plots with 20–29% low and 30–39% medium-low native cover (Table A2).
Native seedling density was higher at inland restoration sites compared to coastal sites throughout the growing season in winter and spring (Table 1 and Table A2). Inland sites contained more native shrub and forb seedlings in both seasons (Table 1 and Table A2). However, there was no significant difference in non-native density between regions (Table 1).
Native species richness was highest in the spring for weeded plots with 20–29% low and 30–39% medium-low initial native cover, suggesting once again the effectiveness of non-native removal for areas with an initial cover of 20–39% natives (Table 2 and Table A3). When evaluating the effect of non-native removal on non-native species richness, we found that non-native species richness was significantly reduced in weeded plots in the winter (Table 2 and Table A3). While non-native species richness remained lower in weeded plots in the spring, the difference was insignificant (Table 2).
Native species richness was significantly greater at inland restoration sites, especially in the spring (Table 2). Interestingly, native species richness was greatest in the inland control plots followed by inland weeded, coastal weeded, and coastal control plots (Table 2 and Table A3). Non-native species richness was also significantly higher at inland restoration sites in the winter (Table 2). Non-native richness remained significantly higher in the spring for inland plots with an initial native cover ranging from 20–49% (Table 2, Table A3).
Non-native plant removal did not significantly impact established shrub volume but did result in significantly more established shrubs (Table A4 and Table A5c). The initial cover of existing native plants did not significantly impact the average volume or number of established shrubs, but the total shrub volume in each plot did vary significantly depending on initial native cover (Table A4). Total shrub volume followed the same pattern of the four initial cover classes, with plots in the highest cover class (50–59% high) having the greatest total volume, while plots in the two lowest cover classes (20–29% low and 30–39% medium-low) had the least (Table A5b). When evaluating the influence of region on established shrub volume and number, we found that inland restoration sites had, on average, significantly smaller shrubs, but significantly more established native shrubs compared to the coastal sites (Figure 4, Table A4 and Table A5a–c). Since we observed several dead established shrubs in our plots in 2014, we decided to assess how shrub mortality was affected by non-native removal, initial native cover, and region. We found that shrub mortality was lower in the weeded plots than in the control plots and lower at coastal sites compared to inland sites (Figure 5, Table A6).

4. Discussion

Non-native removal in areas with existing native cover was successful, but our results revealed some surprising mechanisms behind its success. First, our hypothesis that non-native control would increase native density and species richness was not supported in the early growing season, but higher native density and richness was observed at the end of the growing season, indicating greater native survival in weeded plots. Secondly, non-native removal did not increase established native shrub volume as expected but did increase the number of established shrubs present and reduced mortality, something that was also found in a post-fire non-native removal study [63]. Thirdly, our hypothesis that the effects of non-native removal would vary with site conditions was supported, as removal was more effective inland than at coastal sites. Finally, we identified a threshold of initial native cover (20–39%) for which non-native removal was most effective. The removal of non-natives in areas with higher initial native cover was less effective at increasing the number and diversity of natives, indicating that land stewards could focus removal efforts on the areas with 20–39% native cover to achieve the greatest impact.
Non-native plant removal has been shown to increase native cover and species richness, but only in areas with existing natives that can naturally recolonize weeded areas through native seed dispersal and germination or clonal recruitment [64,65,66,67]. With the removal of non-native species, competition for resources, such as water, space, and light, that are crucial during the early stages of native plant establishment, are reduced [12,20,21,68,69]. Indeed, we found native seedling density and species richness to be higher in weeded plots—something supported by other studies [70,71]. This effect of non-native removal on plant density was most pronounced for native shrub seedlings, which were denser in weeded areas, as opposed to forbs which remained the same. Non-native plants are not always harmful to native plants and may even provide ecosystem services without outcompeting natives [72,73,74]. Low numbers of native forb seedlings might indicate an inadequate seedbank and need to add seeds [7,75,76]. Our method of non-native removal, which included chemical and mechanical control measures, may have had an unintended impact on native forb seedlings. Herbicide residuals or spillovers can reduce recruitment of non-target species, such as native forbs [77]. Mechanical removal often disturbs the soil which may trigger further non-native establishment and negatively impact root systems and the mycorrhizal fungi of the remaining native plants, subsequently affecting plant growth [78,79,80]. The prolonged drought occurring during our study period likely impacted native forb recruitment in both control and weeded plots since forbs are typically more abundant in wet years [39,52].
Contrary to prior studies showing a positive impact of non-native removal on native shrub growth [23,29], non-native removal did not increase established shrub volume in our study. Weeding may not have had an effect because established shrubs can access nutrients and water from deeper depths, ultimately making them better competitors against non-native annuals [81]. Therefore, it is possible that other factors, such as the recent severe drought, may have inhibited shrub growth. Although coastal sage scrub shrub species are adapted to drought, prolonged drought can negatively impact native biomass [82,83]. For example, Llorens et al. (2004) found that stem elongation and shoot growth of mature shrubs was strongly reduced under drought conditions [84]. Native shrubs were larger, on average, in the coastal regions of our study, possibly due to greater moisture near the coast or lower fire frequency in coastal areas [52].
Despite having no effect on established shrub volume, non-native removal significantly increased the number of established shrubs and reduced shrub mortality. The positive impact of non-native removal on established shrub number suggests its importance for reducing competition for resources that would allow germinated shrub seedlings to reach maturity. Non-native plants often grow faster and are better at capitalizing on available resources, ultimately outcompeting native plants and limiting native seedling survival and growth [18,85]. Increased resource availability to native plants following non-native removal may have also contributed to the reduction in shrub mortality in weeded plots. Competition with non-native plants can increase vulnerability of established shrubs to die-off, especially in conditions of high resource stress, such as drought [86]. The drier conditions of inland sites likely exacerbated the influence of drought, possibly contributing to the greater shrub die-off observed inland [87].
We identified 40% as a threshold of native cover above which non-native removal may be less effective. Native density and species richness were highest in weeded plots with lower initial native cover, demonstrating the effectiveness of non-native removal for areas with 20–39% existing native cover. For plots with an initial native cover beyond 39%, there was no significant positive effect of non-native removal on native seedling density and richness. Theoretical work suggests there may be thresholds of native cover beyond which communities may be stuck in a degraded state and not recover [42]. In such degraded sites, removing non-native species without adding natives will simply allow one non-native to replace another [45,88,89]. We did not test non-native removal in areas with less than 20% cover because existing studies indicate these areas would be unlikely to recover. However, our results suggest that a management threshold exists where non-native removal is not as effective for areas with greater than 39% initial native cover. One possible explanation is that areas with higher initial native cover resulted in less available resources for new natives to become established, especially during the drought. Our result indicates the importance of considering site conditions prior to weed removal efforts. Other studies have documented the possibility of harming native communities through weed removal [14,90,91]. Depending on site conditions, limited management resources may be better directed towards other activities [8].
Our study revealed that non-native removal in heavily degraded coastal sage scrub communities increased native cover through increased native seedling recruitment rather than through established shrub growth. Non-native plant removal in degraded areas also helped to support native shrub density, species richness, established shrub number, and to reduce shrub mortality. Climate models predict that our region will experience increasingly severe and common droughts along with higher temperatures [92]. Reducing competition with non-natives may be critical to the survival of a diverse native coastal sage scrub community, and we recommend this approach for transitional areas with 20–39% of existing native cover. Indeed, our finding that non-native removal was not effective in areas with more than 40% shrub cover indicates that these areas would be best left undisturbed by removal efforts. In conclusion, our results indicate the effectiveness of non-native removal for increasing native cover and diversity in areas with a low to medium cover of native species.

Author Contributions

J.C.B., M.L., Q.S., I.O., S.K. and T.E.H. designed and implemented the experiment; E.G., K.R.B., K.T.S., P.M.T., Q.S. and I.O. collected the data; P.M.T. and S.K. analyzed the data; P.M.T., S.K., K.T.S. and J.J.L. wrote the manuscript; all authors edited the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Center for Environmental Biology, which receives support from the Natural Communities Coalition and The Nature Conservancy.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in Dryad at https://doi.org/10.7280/D1168Q.

Acknowledgments

Thanks to staff at the Irvine Ranch Conservancy for helping establish and maintain the experimental plots. Additional thanks to all staff and undergraduate interns from the University of California, Irvine’s Center for Environmental Biology, for their support and assistance with data collection. Finally, thanks to the Nature Conservancy and the Natural Communities Coalition.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A. Soil Composition of Study Sites

Table A1. Soil composition of assisted passive restoration sites. This table presents the soil composition of each restoration site.
Table A1. Soil composition of assisted passive restoration sites. This table presents the soil composition of each restoration site.
RegionRestoration SiteSoil Composition
CoastalCattle Crest71.3% Anaheim loam, 28.7% Cieneba-Rock outcrop complex
CoastalCut Across92.4% Bosanko clay, 7.6 Cieneba sandy loam
CoastalLaguna Laurel100% Yorba cobbly sandy loam
CoastalMoro Ridge100% Myford sandy loam
CoastalStrawberry Farms100% Alo clay
CoastalVeeh Creek87.9% Alo variant clay, 6.4% Capistrano sandy loam, 5.8% Yorba cobbly sandy loam
CoastalWest Canyon97.6% Cieneba sandy loam, 2.4% Myford sandy loam
InlandAgua Chinon100% Balcom clay loam
InlandBlackstar100% Soper gravelly loam
InlandGypsum100% Cieneba-Rock outcrop complex
InlandShoestring100% Calleguas clay loam
InlandUpper Weir100% Alo clay
InlandWest Loma100% Anaheim loam

Appendix B. Tukey Post Hoc Results for Native and Non-Native Seedling Density

Table A2. Tukey post hoc results for native and non-native seedling density. Tukey post hoc results for native density, native shrub density, native forb density, and non-native density on the significant effects of non-native plant removal treatment, native cover class, region, and interactions in the winter and spring. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Data were ln(x + 1)-transformed. Standard error (SE) and letters from the Tukey post hoc tests are included in results tables, with different letters indicating significant differences and shared letters indicating no significant difference amongst groups.
Table A2. Tukey post hoc results for native and non-native seedling density. Tukey post hoc results for native density, native shrub density, native forb density, and non-native density on the significant effects of non-native plant removal treatment, native cover class, region, and interactions in the winter and spring. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Data were ln(x + 1)-transformed. Standard error (SE) and letters from the Tukey post hoc tests are included in results tables, with different letters indicating significant differences and shared letters indicating no significant difference amongst groups.
EffectDependent VariableSeasonTreatmentEstimateSELetter
Treatmentln(x + 1) native densityWinterWeeded1.66220.2446A
WinterControl1.59180.2446A
SpringWeeded0.99120.133A
SpringControl0.75660.133B
EffectDependent VariableSeasonNative Cover ClassTreatmentEstimateSELetter
Treatment x native cover classln(x + 1) native densityWinterMedium-lowWeeded1.82680.3A
WinterHighControl1.76960.3A
WinterLowWeeded1.71830.3A
WinterMedium-highControl1.68330.3A
WinterHighWeeded1.65710.3A
WinterLowControl1.51320.3A
WinterMedium-highWeeded1.44640.3A
WinterMedium-lowControl1.4010.3A
SpringMedium-lowWeeded1.21680.1687A
SpringLowWeeded1.1440.1687AB
SpringHighControl0.94140.1687ABC
SpringMedium-highWeeded0.82230.1703ABC
SpringMedium-highControl0.81850.1687ABC
SpringHighWeeded0.78170.1687ABC
SpringMedium-lowControl0.680.1703BC
SpringLowControl0.58650.1687C
EffectDependent VariableSeasonRegionEstimateSELetter
Regionln(x + 1) native densityWinterInland2.08230.3436A
WinterCoastal1.17160.3181A
SpringInland1.36120.1849A
SpringCoastal0.38660.171B
EffectDependent VariableSeasonTreatmentEstimateSELetter
Treatmentln(x + 1) native shrub densityWinterWeeded1.06940.1523A
WinterControl0.80160.1523B
SpringWeeded0.51420.08285A
SpringControl0.2190.08285B
EffectDependent VariableSeasonRegionEstimateSELetter
Regionln(x + 1) native shrub densityWinterInland1.10670.2102A
WinterCoastal0.76430.1946A
SpringInland0.51450.1024A
SpringCoastal0.21870.09457B
EffectDependent VariableSeasonRegionEstimateSELetter
Regionln(x + 1) native forb densityWinterInland1.65020.3158A
WinterCoastal0.71780.2924B
SpringInland0.98250.169A
SpringCoastal0.15890.1563B
EffectDependent VariableSeasonRegionNative Cover ClassEstimateSELetter
Interaction between region and initial native cover classln(x + 1) native forb densityWinterInlandHigh1.80960.3654A
WinterInlandMedium-low1.78470.3654A
WinterInlandLow1.53150.3654A
WinterInlandMedium-high1.4750.3654A
WinterCoastalLow0.95360.3383A
WinterCoastalMedium-high0.79280.3383A
WinterCoastalHigh0.75690.3383A
WinterCoastalMedium-low0.36810.3383A
SpringInlandMedium-low1.22560.1894A
SpringInlandHigh0.94920.1884AB
SpringInlandMedium-high0.92210.1894AB
SpringInlandLow0.83320.1884ABC
SpringCoastalMedium-high0.23840.1744BC
SpringCoastalHigh0.21370.1744BC
SpringCoastalLow0.11950.1744C
SpringCoastalMedium-low0.064070.1744C
EffectDependent VariableSeasonTreatmentEstimateSELetter
Treatmentln(x + 1) non-native densityWinterControl3.60990.2253A
WinterWeeded2.66370.2253B
SpringControl2.61570.207A
SpringWeeded1.82460.207B
EffectDependent VariableSeasonNative Cover ClassEstimateSELetter
Initial native cover classln(x + 1) non-native densityWinterMedium-low3.52930.2721A
WinterLow3.30510.2721A
WinterHigh2.89460.2721A
WinterMedium-high2.81820.2721A
SpringMedium-low2.52560.2384A
SpringLow2.46080.2376AB
SpringHigh2.0150.2376AB
SpringMedium-high1.87910.2384B

Appendix C. Tukey Post Hoc Results for Native and Non-Native Species Richness

Table A3. Tukey post hoc results for native and non-native species richness. Results for native and non-native species richness on the significant effects of non-native plant removal treatment, native cover class, region, and interactions in the winter and spring. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Data were sqrt (x + 1)-transformed. Standard error (SE) and letters from the Tukey post hoc tests are included in results tables, with different letters indicating significant differences and shared letters indicating no significant difference amongst groups.
Table A3. Tukey post hoc results for native and non-native species richness. Results for native and non-native species richness on the significant effects of non-native plant removal treatment, native cover class, region, and interactions in the winter and spring. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Data were sqrt (x + 1)-transformed. Standard error (SE) and letters from the Tukey post hoc tests are included in results tables, with different letters indicating significant differences and shared letters indicating no significant difference amongst groups.
EffectDependent VariableSeasonNative Cover ClassTreatmentEstimateSELetter
Treatment x initial native cover classsqrt (x + 1) native species richnessWinterHighControl1.73020.1206A
WinterMedium-lowWeeded1.66140.1206A
WinterLowWeeded1.6450.1206A
WinterMedium-highControl1.62010.1206A
WinterMedium-highWeeded1.59320.1206A
WinterMedium-lowControl1.560.1206A
WinterLowControl1.53070.1206A
WinterHighWeeded1.52550.1206A
SpringMedium-lowWeeded1.43180.0686A
SpringLowWeeded1.42870.0686AB
SpringHighControl1.40420.0686ABC
SpringMedium-highControl1.37530.0686ABC
SpringMedium-highWeeded1.29510.06909ABC
SpringMedium-lowControl1.29410.06909ABC
SpringLowControl1.25240.0686BC
SpringHighWeeded1.24160.0686C
EffectDependent VariableSeasonRegionEstimateSELetter
Regionsqrt (x + 1) native species richnessWinterInland1.78820.1481A
WinterCoastal1.42830.1371A
SpringInland1.54090.08366A
SpringCoastal1.13990.0774B
EffectDependent VariableSeasonRegionTreatmentEstimateSELetter
Region x Treatmentsqrt (x + 1) native species richnessWinterInlandControl1.82050.1526A
WinterInlandWeeded1.75590.1526A
WinterCoastalWeeded1.45660.1412A
WinterCoastalControl1.39990.1412A
SpringInlandControl1.57310.08635A
SpringInlandWeeded1.50870.08635A
SpringCoastalWeeded1.18990.07985B
SpringCoastalControl1.08990.07985B
EffectDependent VariableSeasonTreatmentEstimateSELetter
Treatmentsqrt (x + 1) non-native species richnessWinterControl1.84190.05725A
WinterWeeded1.73910.05725B
SpringControl1.62850.06289A
SpringWeeded1.54940.06289A
EffectDependent VariableSeasonRegionEstimateSELetter
Regionsqrt (x + 1) non-native species richnessWinterInland1.90980.07674A
WinterCoastal1.67120.07105B
SpringInland1.6690.08582A
SpringCoastal1.50890.07937A
EffectDependent VariableSeasonRegionNative Cover ClassEstimateSELetter
Region x initial native cover classsqrt (x + 1) non-native species richnessWinterInlandMedium-low2.02470.09697A
WinterInlandLow1.89930.09697AB
WinterInlandMedium-high1.88410.09697AB
WinterInlandHigh1.8310.09697AB
WinterCoastalMedium-low1.72010.08978AB
WinterCoastalHigh1.71430.08978AB
WinterCoastalLow1.65540.08978AB
WinterCoastalMedium-high1.59510.08978B
SpringInlandMedium-high1.73640.1045A
SpringInlandMedium-low1.70810.1045A
SpringInlandLow1.69920.104A
SpringCoastalMedium-low1.5920.09624A
SpringCoastalLow1.5920.09624A
SpringInlandHigh1.53230.104A
SpringCoastalHigh1.50050.09624A
SpringCoastalMedium-high1.35130.09624A

Appendix D. ANOVA Results for Established Shrub Metrics

Table A4. ANOVA results for established shrub metrics. Established shrub metrics include data on mean volume, total volume, and number of shrubs collected at the original ten restoration sites in 2012 and 2014. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Mean shrub volume and shrub number data were ln(x)-transformed. Shaded rows highlight effects that were significant (p < 0.05).
Table A4. ANOVA results for established shrub metrics. Established shrub metrics include data on mean volume, total volume, and number of shrubs collected at the original ten restoration sites in 2012 and 2014. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Mean shrub volume and shrub number data were ln(x)-transformed. Shaded rows highlight effects that were significant (p < 0.05).
Response VariableEffectNum DFDen DFF Valuep Value
Mean shrub volumeTreatment11353.280.0723
Native cover class31351.20.3108
Native cover class × treatment31351.060.3682
Region113517.5<0.0001
Region × treatment11351.490.2248
Region × native cover class31350.070.9747
Region × native cover Class × treatment31350.760.5166
Total shrub volumeTreatment11353.120.0796
Native cover class31358.64<0.0001
Native cover class × treatment31350.190.9031
Region11350.730.3953
Region × treatment11350.590.4455
Region × native Cover Class31352.390.0718
Region × native Cover Class × treatment31350.210.888
Shrub numberTreatment11359.950.002
Native cover class31351.740.1626
Native cover class × treatment31350.850.468
Region113516.71<0.0001
Region × treatment11351.010.316
Region × native cover class31350.940.4244
Region × native cover Class × treatment31351.760.157

Appendix E. Tukey Post Hoc Results for Established Shrub Metrics

Table A5. Tukey post hoc results for established shrub metrics. Results for (a) mean shrub volume, (b) total shrub volume, and (c) number of established shrubs on the effects of non-native plant removal treatment, native cover class, region, and all interactions. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Mean shrub volume and shrub number data were ln(x)-transformed. Standard error (SE) and letters from the Tukey post hoc tests are included in results tables, with different letters indicating significant differences and shared letters indicating no significant difference amongst groups.
Table A5. Tukey post hoc results for established shrub metrics. Results for (a) mean shrub volume, (b) total shrub volume, and (c) number of established shrubs on the effects of non-native plant removal treatment, native cover class, region, and all interactions. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Mean shrub volume and shrub number data were ln(x)-transformed. Standard error (SE) and letters from the Tukey post hoc tests are included in results tables, with different letters indicating significant differences and shared letters indicating no significant difference amongst groups.
(a) Tukey–Kramer post hoc results for ln(x) mean established shrub volume
Effect of Region
RegionEstimateSELetter
Coastal5.55340.2199A
Inland4.2530.2197B
(b) Tukey–Kramer post hoc results for total established shrub volume
Effect of Initial Native Cover Class
Native Cover ClassEstimateSELetter
High24.67621.9698A
Medium-high21.64371.9698AB
Medium-low17.50531.9698B
Low17.47241.9767B
(c) Tukey–Kramer post hoc results for ln(x) number of established shrubs
Effect of Treatment
TreatmentEstimateSELetter
Weeded2.78570.1437A
Control2.43560.1435B
Effect of Region
RegionEstimateSELetter
Inland3.1520.1872A
Coastal2.06940.1873B

Appendix F. Logistic Regression Results for Established Shrub Mortality

Table A6. Logistic regression results for established shrub mortality. Shrub mortality was sampled at all thirteen restoration sites in 2014. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Shaded rows highlight effects that were significant (p < 0.05).
Table A6. Logistic regression results for established shrub mortality. Shrub mortality was sampled at all thirteen restoration sites in 2014. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Shaded rows highlight effects that were significant (p < 0.05).
Response VariableEffectEstimateSEZ Valuep Value
Shrub mortality(Intercept)−1.223290.17106−7.15118.61 × 10−13
Treatment−0.351820.12274−2.86630.00415
Native cover class−0.014460.5546−0.26070.79431
Region−1.054320.14839−7.1051.2 × 10−12

References

  1. Cowling, R.M.; Rundel, P.W.; Lamont, B.B.; Arroyo, M.K.; Arianoutsou, M. Plant diversity in mediterranean-climate regions. Trends Ecol. Evol. 1996, 11, 362–366. [Google Scholar] [CrossRef]
  2. Medail, F.; Quezel, P. Hot-Spots Analysis for Conservation of Plant Biodiversity in the Mediterranean Basin. Ann. Mo. Bot. Gard. 1997, 84, 112–127. [Google Scholar] [CrossRef]
  3. Sala, O.E.; Chapin, F.S.; Armesto, J.J.; Berlow, E.; Bloomfield, J.; Dirzo, R.; Huber-Sanwald, E.; Huenneke, L.F.; Jackson, R.B.; Kinzig, A.; et al. Global Biodiversity Scenarios for the Year 2100. Science 2000, 287, 1770–1774. [Google Scholar] [CrossRef] [PubMed]
  4. Talluto, M.V.; Suding, K.N. Historical change in coastal sage scrub in southern California, USA in relation to fire frequency and air pollution. Landsc. Ecol. 2008, 23, 803–815. [Google Scholar] [CrossRef]
  5. Kimball, S.; Goulden, M.L.; Suding, K.N.; Parker, S. Altered water and nitrogen input shifts succession in a southern California coastal sage community. Ecol. Appl. 2014, 24, 1390–1404. [Google Scholar] [CrossRef] [PubMed]
  6. Syphard, A.D.; Brennan, T.J.; Keeley, J.E. Extent and drivers of vegetation type conversion in Southern California chaparral. Ecosphere 2019, 10, 14. [Google Scholar] [CrossRef]
  7. Cione, N.K.; Padgett, P.E.; Allen, E.B. Restoration of a native shrubland impacted by exotic grasses, frequent fire, and nitrogen deposition in southern California. Restor. Ecol. 2002, 10, 376–384. [Google Scholar] [CrossRef]
  8. Kimball, S.; Lulow, M.; Sorenson, Q.; Balazs, K.; Fang, Y.; Davis, S.J.; O’Connell, M.; Huxman, T.E. Cost-effective ecological restoration. Restor. Ecol. 2015, 23, 800–810. [Google Scholar] [CrossRef]
  9. Schmidt, K.T.; Maltz, M.; Ta, P.; Khalili, B.; Weihe, C.; Phillips, M.; Aronson, E.; Lulow, M.; Long, J.; Kimball, S. Identifying Mechanisms for Successful Ecological Restoration with Salvaged Topsoil in Coastal Sage Scrub Communities. Diversity 2020, 12, 150. [Google Scholar] [CrossRef]
  10. De Steven, D.; Sharitz, R.R.; Singer, J.H.; Barton, C.D. Testing a passive revegetation approach for restoring coastal plain depression wetlands. Restor. Ecol. 2006, 14, 452–460. [Google Scholar] [CrossRef]
  11. Crouzeilles, R.; Prevedello, J.A.; de Souza Lima Figueiredo, M.; Lorini, M.L.; Grelle, C.E.V. The effect of the number, size and isolation of patches along a gradient of native vegetation cover: How can we increment habitat availability? Landsc. Ecol. 2014, 29, 479–489. [Google Scholar] [CrossRef]
  12. Eliason, S.A.; Allen, E.B. Exotic grass competition in suppressing native shrubland re-establishment. Restor. Ecol. 1997, 5, 245–255. [Google Scholar] [CrossRef]
  13. Shono, L.; Cadaweng, E.A.; Durst, P.B. Application of Assisted Natural Regeneration to Restore Degraded Tropical Forestlands. Restor. Ecol. 2007, 15, 620–626. [Google Scholar] [CrossRef]
  14. de Mesquita, C.P.B.; Solon, A.J.; Barfield, A.; Mastrangelo, C.F.; Tubman, A.J.; Vincent, K.; Porazinska, D.L.; Hufft, R.A.; Shackelford, N.; Suding, K.N.; et al. Adverse impacts of Roundup on soil bacteria, soil chemistry and mycorrhizal fungi during restoration of a Colorado grassland. Appl. Soil Ecol. 2023, 185, 104778. [Google Scholar] [CrossRef]
  15. Morrison, E.; Lindell, C. Active or Passive Forest Restoration? Assessing Restoration Alternatives with Avian Foraging Behavior. Restor. Ecol. 2010, 19, 170–177. [Google Scholar] [CrossRef]
  16. Holl, K.; Aide, T. When and where to actively restore ecosystems? For. Ecol. Manag. 2011, 261, 1558–1563. [Google Scholar] [CrossRef]
  17. Ruwanza, S.; Gaertner, M.; Esler, K.; Richardson, D. The effectiveness of active and passive restoration on recovery of indigenous vegetation in riparian zones in the Western Cape, South Africa: A preliminary assessment. S. Afr. J. Bot. 2013, 88, 132–141. [Google Scholar] [CrossRef]
  18. Bell, C.E.; Allen, E.B.; Weathers, K.A.; McGiffen, M. Simple Approaches to Improve Restoration of Coastal Sage Scrub Habitat in Southern California. Nat. Areas J. 2016, 36, 20–28. [Google Scholar] [CrossRef]
  19. Dyer, A.R.; Rice, K.J. Effects of competition on resource availability and growth of a California bunchgrass. Ecology 1999, 80, 2697–2710. [Google Scholar] [CrossRef]
  20. Clary, J.; Save, R.; Biel, C.; De Herralde, F. Water relations in competitive interactions of Mediterranean grasses and shrubs. Ann. Appl. Biol. 2004, 144, 149–155. [Google Scholar] [CrossRef]
  21. Wainwright, C.E.; Wolkovich, E.M.; Cleland, E.E. Seasonal priority effects: Implications for invasion and restoration in a semi-arid system. J. Appl. Ecol. 2012, 49, 234–241. [Google Scholar] [CrossRef]
  22. Balshor, B.J.; Garrambone, M.S.; Austin, P.; Balazs, K.R.; Weihe, C.; Martiny, J.B.; Huxman, T.E.; McCollum, J.R.; Kimball, S. The effect of soil inoculants on seed germination of native and invasive species. Botany 2016, 95, 469–480. [Google Scholar] [CrossRef]
  23. Esch, E.; Ashbacher, A.; Kopp, C.; Cleland, E. Competition reverses the response of shrub seedling mortality and growth along a soil moisture gradient. J. Ecol. 2018, 106, 2096–2108. [Google Scholar] [CrossRef]
  24. Morgan, J.W. Patterns of invasion of an urban remnant of a species-rich grassland in southeastern Australia by non-native plant species. J. Veg. Sci. 1998, 9, 181–190. [Google Scholar] [CrossRef]
  25. Molinari, N.A.; D’Antonio, C.M. Where have all the wildflowers gone? The role of exotic grass thatch. Biol. Invasions 2020, 22, 957–968. [Google Scholar] [CrossRef]
  26. Chen, B.M.; D’Antonio, C.M.; Molinari, N.; Peng, S.L. Mechanisms of influence of invasive grass litter on germination and growth of coexisting species in California. Biol. Invasions 2018, 20, 1881–1897. [Google Scholar] [CrossRef]
  27. Molinari, N.A.; D’Antonio, C.M. Structural, compositional and trait differences between native- and non-native-dominated grassland patches. Funct. Ecol. 2014, 28, 745–754. [Google Scholar] [CrossRef]
  28. Uebel, K.; Wison, K.A.; Shoo, L.P. Assisted natural regeneration accelerates recovery of highly disturbed rainforest. Ecol. Manag. Restor. 2017, 18, 231–238. [Google Scholar] [CrossRef]
  29. D’Antonio, C.M.; Hughes, R.F.; Mack, M.; Hitchcock, D.; Vitousek, P.M. The response of native species to removal of invasive exotic grasses in a seasonally dry Hawaiian woodland. J. Veg. Sci. 1998, 9, 699–712. [Google Scholar] [CrossRef]
  30. Baylis, A.D. Why glyphosate is a global herbicide: Strengths, weaknesses and prospects. Pest Manag. Sci. 2000, 56, 299–308. [Google Scholar] [CrossRef]
  31. Reid, A.M.; Morin, L.; Downey, P.O.; French, K.; Virtue, J.G. Does invasive plant management aid the restoration of natural ecosystems? Biol. Conserv. 2009, 142, 2342–2349. [Google Scholar] [CrossRef]
  32. Westman, W.E. Factors Influencing the Distribution of Species of Californian Coastal Sag Scrub. Ecology 1981, 62, 439–455. [Google Scholar] [CrossRef]
  33. Kimball, S.; Lulow, M.E.; Balazs, K.R.; Huxman, T.E. Predicting drought tolerance from slope aspect preference in restored plant communities. Ecol. Evol. 2017, 7, 3123–3131. [Google Scholar] [CrossRef]
  34. Davis, M.A.; Pelsor, M. Experimental support for a resource-based mechanistic model of invasibility. Ecol. Lett. 2001, 4, 421–428. [Google Scholar] [CrossRef]
  35. Blumenthal, D.; Mitchell, C.E.; Pysek, P.; Jarosík, V. Synergy between pathogen release and resource availability in plant invasion. Proc. Natl. Acad. Sci. USA 2009, 106, 7899–7904. [Google Scholar] [CrossRef]
  36. Vilà, M.; Espinar, J.L.; Hejda, M.; E Hulme, P.; Jarošík, V.; Maron, J.L.; Pergl, J.; Schaffner, U.; Sun, Y.; Pyšek, P. Ecological impacts of invasive alien plants: A meta-analysis of their effects on species, communities and ecosystems. Ecol. Lett. 2011, 14, 702–708. [Google Scholar] [CrossRef]
  37. Funk, J.L.; Vitousek, P.M. Resource-use efficiency and plant invasion in low-resource systems. Nature 2007, 446, 1079–1081. [Google Scholar] [CrossRef]
  38. Kimball, S.; Gremer, J.R.; Barron-Gafford, G.A.; Angert, A.L.; Huxman, T.E.; Venable, D.L. High water-use efficiency and growth contribute to success of non-native Erodium cicutarium in a Sonoran Desert winter annual community. Conserv. Physiol. 2014, 2, cou006. [Google Scholar] [CrossRef]
  39. Dudney, J.; Hallett, L.M.; Larios, L.; Farrer, E.C.; Spotswood, E.N.; Stein, C.; Suding, K.N. Lagging behind: Have we overlooked previous-year rainfall effects in annual grasslands? J. Ecol. 2017, 105, 484–495. [Google Scholar] [CrossRef]
  40. Mazzochini, G.G.; Lira-Martins, D.; de Barros, F.V.; Oliveira, A.C.C.; Xavier, R.O.; Furtado, M.N.; Verona, L.S.; Viani, R.A.G.; Rowland, L.; Oliveira, R.S. Effects of grass functional diversity on invasion success by exotic grasses in Cerrado grasslands. J. Appl. Ecol. 2023. early view. [Google Scholar] [CrossRef]
  41. Hobbs, R.; Norton, D. Towards a Conceptual Framework for Restoration Ecology. Restor. Ecol. 1996, 4, 93–110. [Google Scholar] [CrossRef]
  42. Suding, K.N.; Gross, K.L.; Houseman, G.R. Alternative states and positive feedbacks in restoration ecology. Trends Ecol. Evol. 2004, 19, 46–53. [Google Scholar] [CrossRef]
  43. Marchante, H.; Freitas, H.; Hoffmann, J.H. The potential role of seed banks in the recovery of dune ecosystems after removal of invasive plant species. Appl. Veg. Sci. 2011, 14, 107–119. [Google Scholar] [CrossRef]
  44. Conlisk, E.; Swab, R.; Martinez-Berdeja, A.; Daugherty, M.P. Post-Fire Recovery in Coastal Sage Scrub: Seed Rain and Community Trajectory. PLoS ONE 2016, 11, e0162777. [Google Scholar] [CrossRef]
  45. Cox, R.; Allen, E. Composition of soil seed banks in southern California coastal sage scrub and adjacent exotic grassland. Plant Ecol. 2008, 198, 37–46. [Google Scholar] [CrossRef]
  46. Young, S.L.; Hamerlynch, E.P. Patterning ecological restoration after weeds. Restor. Ecol. 2022, 31, e13841. [Google Scholar] [CrossRef]
  47. Griffoul, E. The Effectiveness of Passive Restoration: Influence of Initial Cover on Success. Master’s Thesis, University of California, Irvine, CA, USA, 2017. [Google Scholar]
  48. Allen, E.B.; Cox, R.D.; Tennant, T.; Kee, S.N.; Deutschman, D.H. Landscape restoration in southern California forblands: Response of abandoned farmland to invasive annual grass control. Isr. J. Plant Sci. 2005, 53, 237–245. [Google Scholar] [CrossRef]
  49. Medrano, H.; Flexas, J.; Galmes, J. Variability in water use efficiency at the leaf level among Mediterranean plants with different growth forms. Plant Soil 2009, 317, 17–29. [Google Scholar] [CrossRef]
  50. Galmés, J.; Cifre, J.; Medrano, H.; Flexas, J. Modulation of relative growth rate and its components by water stress in Mediterranean species with different growth forms. Oecologia 2005, 145, 21–31. [Google Scholar] [CrossRef]
  51. Seastedt, T.R.; Hobbs, R.J.; Suding, K.M. Management of novel ecostystems: Are novel approaches required? Front. Ecol. Environ. 2008, 6, 547–553. [Google Scholar] [CrossRef]
  52. Kimball, S.; Principe, Z.; Deutschman, D.; Strahm, S.; Huxman, T.; Lulow, M.; Balazs, K. Resistance and resilience: Ten years of monitoring shrub and prairie communities in Orange County, CA, USA. Ecosphere 2018, 9, e02212. [Google Scholar] [CrossRef]
  53. Keeley, J.E.; Baer-Keeley, M.; Fotheringham, C.J. Alien plant dynamics following fire in Mediterranean-climate California shrublands. Ecol. Appl. 2005, 15, 2109–2125. [Google Scholar] [CrossRef]
  54. Goldstein, L.J.; Suding, K.N. Applying competition theory to invasion: Resource impacts indicate invasion mechanisms in California shrublands. Biol. Invasions 2014, 16, 191–203. [Google Scholar] [CrossRef]
  55. Wakefield, Z.R.; Cavalcanti, A.R.O.; Driessen, L.; Jaramillo, A.; Crane, E.J.; Richetta, G.; Meyer, W.M. Effects of Mustard Invasions on Soil Microbial Abundances and Fungal Assemblages in Southern California. Diversity 2023, 15, 50. [Google Scholar] [CrossRef]
  56. Oduor, A.M.O.; van Kleunen, M.; Stift, M. Allelopathic effects of native and invasive Brassica nigra do not support the novel-weapons hypothesis. Am. J. Bot. 2020, 107, 1106–1113. [Google Scholar] [CrossRef]
  57. Dewees, S.L.; D’Antonio, C.M.; Molinari, N. Determining potential drivers of vegetation change in a Mediterranean environment. Ecosphere 2022, 13, e4313. [Google Scholar] [CrossRef]
  58. Kimball, S.; Lulow, M.E.; Mooney, K.A.; Sorenson, Q.M. Establishment and Management of Native Functional Groups in Restoration. Restor. Ecol. 2014, 22, 81–88. [Google Scholar] [CrossRef]
  59. USDA. Soil Quality Test Kit Guide; USDA: Washington, DC, USA, 1999.
  60. Kirkpatrick, J.B.; Hutchinson, C.F. The Environmental Relationships of Californian Coastal Sage Scrub and Some of its Component Communities and Species. J. Biogeogr. 1980, 7, 23–28. [Google Scholar] [CrossRef]
  61. Dave Bramlett & Jones & Stokes Associates, Inc. Methods Used to Survery the Vegetation of Orange County Parks and Open Space Areas and The Irvine Company Property; Unpublished report prepared for County of Orange; Environmental Management Agency: Santa Ana, CA, USA, 1993. [Google Scholar]
  62. SAS Institute 2012 Software; Version 94; S.A.S. Institute Inc.: Cary, NC, USA, 2012.
  63. Thomson, D.M.; Meyer, W.M.; Whitcomb, I.F. Non-native plant removal and high rainfall years promote post-fire recovery of Artemisia californica in southern California sage scrub. PLoS ONE 2021, 16, e0254398. [Google Scholar] [CrossRef]
  64. O’Loughlin, L.S.; Panetta, F.D.; Gooden, B. Identifying thresholds in the impacts of an invasive groundcover on native vegetation. Sci. Rep. 2021, 11, 20512. [Google Scholar] [CrossRef]
  65. DeMeester, J.; Richter, D. Restoring restoration: Removal of the invasive plant Microstegium vimineum from a North Carolina wetland. Biol. Invasions 2010, 12, 781–793. [Google Scholar] [CrossRef]
  66. HilleRisLambers, J.; Yelenik, S.; Colman, B.; Levine, J. California annual grass invaders: The drivers or passengers of change? J. Ecol. 2010, 98, 1147–1156. [Google Scholar] [CrossRef]
  67. Leege, L.; Kilgore, J. Recovery of Foredune and Blowout Habitats in a Freshwater Dune Following Removal of Invasive Austrian Pine (Pinus nigra). Restor. Ecol. 2014, 22, 641–648. [Google Scholar] [CrossRef]
  68. DiVittorio, C.; Corbin, J.; D’Antonio, C. Spatial and Temporal Patterns of Seed Dispersal: An Important Determinant of Grassland Invasion. Ecol. Appl. 2007, 17, 311–316. [Google Scholar] [CrossRef]
  69. Padilla, F.; Pugnaire, F. Rooting depth and soil moisture control Mediterranean woody seedling survival during drought. Funct. Ecol. 2007, 21, 489–495. [Google Scholar] [CrossRef]
  70. Biggerstaff, M.S.; Beck, C.W. Effects of Method of English Ivy Removal and Seed Addition on Regeneration of Vegetation in a Southeastern Piedmont Forest. Am. Midl. Nat. 2007, 158, 206–220. [Google Scholar] [CrossRef]
  71. Flory, S.L.; Clay, K. Invasive plant removal method determines native plant community responses. J. Appl. Ecol. 2009, 46, 434–442. [Google Scholar] [CrossRef]
  72. Castro-Díez, P.; Vaz, A.S.; Silva, J.S.; Loo, M.; Alonso, A.; Aponte, C.; Bayón, A.; Bellingham, P.J.; Chiuffo, M.C.; DiManno, N.; et al. Global effects of non-native tree species on multiple ecosystem services. Biol. Rev. 2019, 94, 1477–1501. [Google Scholar] [CrossRef]
  73. Fehr, V.; Buitenwerf, R.; Svenning, J.C. Non-native palms (Arecaceae) as generators of novel ecosystems: A global assessment. Divers. Distrib. 2020, 26, 1523–1538. [Google Scholar] [CrossRef]
  74. Arrington, A. Urban foraging of five non-native plants in NYC: Balancing ecosystem services and invasive species management. Urban For. Urban Green. 2021, 58, 126896. [Google Scholar] [CrossRef]
  75. DiTomaso, J.M. Invasive Weeds in Rangelands: Species, Impacts, and Management. Weed Sci. 2000, 48, 255–265. [Google Scholar] [CrossRef]
  76. Seabloom, E.W.; Borer, E.T.; Boucher, V.L.; Burton, R.S.; Cottingham, K.L.; Goldwasser, L.; Gram, W.K.; Kendall, B.E.; Micheli, F. Competition, seed limitation, disturbance, and reestablishment of California native annual forbs. Ecol. Appl. 2003, 13, 575–592. [Google Scholar] [CrossRef]
  77. Crone, E.E.; Marler, M.; Pearson, D.E. Non-target effects of broadcast leaf herbicide on a native perennial forb; a demographic framework for assessing and minimizing impacts. J. Appl. Ecol. 2009, 46, 673–682. [Google Scholar] [CrossRef]
  78. McLellan, A.J.; Fitter, A.H.; Law, R. On Decaying Roots, Mycorrhizal Colonization and the Design of Removal Experiments. J. Ecol. 1995, 83, 225. [Google Scholar] [CrossRef]
  79. Burke, M.J.W.; Grime, J.P. An experimental study of plant community invasibility. Ecology 1996, 77, 776–790. [Google Scholar] [CrossRef]
  80. Kyle, G.P.; Beard, K.H.; Kulmatiski, A. Reduced soil compaction enhances establishment of non-native plant species. Plant Ecol. 2007, 193, 223–232. [Google Scholar] [CrossRef]
  81. Goldstein, L.J.; Suding, K.N. Intra-annual rainfall regime shifts competitive interactions between coastal sage scrub and invasive grasses. Ecology 2014, 95, 425–435. [Google Scholar] [CrossRef]
  82. Llorens, L.; Penuelas, J.; Estiarte, M. Ecophysiological responses of two Mediterranean shrubs, Erica multiflora and Globularia alypum, to experimentally drier and warmer conditions. Physiol. Plant. 2003, 119, 231–243. [Google Scholar] [CrossRef]
  83. Okin, G.S.; Dong, C.; Willis, K.S.; Gillespie, T.W.; MacDonald, G.M. The Impact of Drought on Native Southern California Vegetation: Remote Sensing Analysis Using MODIS-Derived Time Series. J. Geophys. Res. Biogeosci. 2018, 123, 1927–1939. [Google Scholar] [CrossRef]
  84. Llorens, L.; Penuelas, J.; Estiarte, M.; Bruna, P. Contrasting Growth Changes in Two Dominant Species of a Mediterranean Shrubland Submitted to Experimental Drought and Warming. Ann. Bot. 2004, 94, 843–853. [Google Scholar] [CrossRef]
  85. Dawson, W.; Rohr, R.P.; van Kleunen, M.; Fischer, M. Alien pant species with a wider global distribution are better able to capitalize on increased resource availability. New Phytol. 2012, 194, 859–867. [Google Scholar] [CrossRef]
  86. Winkler, D.E.; Belnap, J.; Hoover, D.; Reed, S.C.; Duniway, M.C. Shrub persistence and increased grass mortality in response to drought in dryland systems. Glob. Change Biol. 2019, 25, 3121–3135. [Google Scholar] [CrossRef]
  87. Adams, H.D.; Guardiola-Claramonte, M.; Barron-Gafford, G.A.; Villegas, J.C.; Breshears, D.D.; Zou, C.B.; Troch, P.A.; Huxman, T.E. Temperature sensitivity of drought-induced tree mortality portends increased regional die-off under global-change-type drought. Proc. Natl. Acad. Sci. USA 2009, 106, 7063–7066. [Google Scholar] [CrossRef]
  88. Seabloom, E.W.; Harpole, W.S.; Reichman, O.J.; Tilman, D. Invasion, competitive dominance, and resource use by exotic and native California grassland species. Proc. Natl. Acad. Sci. USA 2003, 100, 13384–13389. [Google Scholar] [CrossRef]
  89. Cox, R.D.; Allen, E.B. The roles of exotic grasses and forbs when restoring native species to highly invaded southern California annual grassland. Plant Ecol. 2011, 212, 1699–1707. [Google Scholar] [CrossRef]
  90. Marrs, R.H.; Williams, C.T.; Frost, A.J.; Plant, R.A. Assessment of the effects of herbicide spray drift on a range of plant species of conservation interest. Environ. Pollut. 1989, 59, 71–86. [Google Scholar] [CrossRef]
  91. Ferreira, M.F.; Torres, C.; Bracamonte, E.; Galetto, L. Glyphosate affects the susceptibility of non-target native plant species according to their stage of development and degree of exposure in the landscape. Sci. Total Environ. 2023, 865, 161091. [Google Scholar] [CrossRef]
  92. Dai, A.G. Increasing drought under global warming in observations and models. Nat. Clim. Change 2013, 3, 52–58. [Google Scholar] [CrossRef]
Figure 1. Map of study sites. All sites are located within Irvine Ranch Natural Landmarks in Orange County, CA, USA with ten sites (Agua Chinon, Blackstar, Cattle Crest, Laguna Laurel, Shoestring, Strawberry Farms, Weir, West Canyon, West Loma, and Veeh Creek) originally established in 2010 and three sites (Cut Across, Gypsum, and Moro Ridge) added later in 2014.
Figure 1. Map of study sites. All sites are located within Irvine Ranch Natural Landmarks in Orange County, CA, USA with ten sites (Agua Chinon, Blackstar, Cattle Crest, Laguna Laurel, Shoestring, Strawberry Farms, Weir, West Canyon, West Loma, and Veeh Creek) originally established in 2010 and three sites (Cut Across, Gypsum, and Moro Ridge) added later in 2014.
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Figure 2. Photographs showing (a) non-native annual grassland with some coastal sage scrub interspersed, (b) coastal sage scrub adjacent to non-native grassland, and (c) a close-up of the Shoestring Canyon site, showing native and non-native species interspersed. Photos by Kristin Barbour (a,c) and Priscilla Ta (c).
Figure 2. Photographs showing (a) non-native annual grassland with some coastal sage scrub interspersed, (b) coastal sage scrub adjacent to non-native grassland, and (c) a close-up of the Shoestring Canyon site, showing native and non-native species interspersed. Photos by Kristin Barbour (a,c) and Priscilla Ta (c).
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Figure 3. ANOVA results on the effects of non-native plant removal on seedling recruitment of (a) all natives, (b) native shrubs, (c) native forbs, and (d) all non-natives. Plant density data were collected over the course of a growing season for three years (2014–2016). Results are reported as mean ± SE. Significant factors are included in the graphs with * signifying p < 0.05, ** signifying p < 0.01, and *** signifying p < 0.0001.
Figure 3. ANOVA results on the effects of non-native plant removal on seedling recruitment of (a) all natives, (b) native shrubs, (c) native forbs, and (d) all non-natives. Plant density data were collected over the course of a growing season for three years (2014–2016). Results are reported as mean ± SE. Significant factors are included in the graphs with * signifying p < 0.05, ** signifying p < 0.01, and *** signifying p < 0.0001.
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Figure 4. ANOVA results on the effects of non-native plant removal across region on (a) mean volume and (b) number of established native shrubs. Shrub data were collected in 2012 and 2014 at the ten original restoration sites. Results are reported as mean ± SE. Significant main effects are reported in the text box with ** indicating p < 0.01, and *** indicating p < 0.0001. The treatment-by-region interaction was not significant for either analysis and so was not listed.
Figure 4. ANOVA results on the effects of non-native plant removal across region on (a) mean volume and (b) number of established native shrubs. Shrub data were collected in 2012 and 2014 at the ten original restoration sites. Results are reported as mean ± SE. Significant main effects are reported in the text box with ** indicating p < 0.01, and *** indicating p < 0.0001. The treatment-by-region interaction was not significant for either analysis and so was not listed.
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Figure 5. The effect of non-native plant removal across region on established native shrub mortality. Shrub mortality was assessed once in 2014 for all thirteen restoration sites. Results are expressed as a percentage of dead shrubs. Significance levels are marked by asterisks, with ** representing p < 0.01, and *** representing p < 0.0001. The treatment-by-region interaction was included in the model but was not significant (p > 0.05).
Figure 5. The effect of non-native plant removal across region on established native shrub mortality. Shrub mortality was assessed once in 2014 for all thirteen restoration sites. Results are expressed as a percentage of dead shrubs. Significance levels are marked by asterisks, with ** representing p < 0.01, and *** representing p < 0.0001. The treatment-by-region interaction was included in the model but was not significant (p > 0.05).
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Table 1. Results from repeated measures mixed model ANOVA for native, native shrub, native forb, and non-native density. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Shaded rows highlight effects that were significant (p < 0.05). Data were ln(x + 1)-transformed.
Table 1. Results from repeated measures mixed model ANOVA for native, native shrub, native forb, and non-native density. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Shaded rows highlight effects that were significant (p < 0.05). Data were ln(x + 1)-transformed.
Response VariableSeasonEffectNum DFDen DFF Valuep Value
Native densityWinterTreatment12850.250.6198
Native cover class32850.190.9014
Native cover class × treatment32851.130.3374
Region12853.780.0527
Region × treatment12851.960.1623
Region × native cover class32850.840.4713
Region × native cover class × treatment32850.820.4856
SpringTreatment12837.570.0063
Native cover class32830.390.7583
Native cover class × treatment32834.650.0035
Region128314.970.0001
Region × treatment12831.590.2081
Region × native cover class32831.470.224
Region × native cover class × treatment32830.410.7439
Native shrub densityWinterTreatment12856.730.01
Native cover class32852.120.098
Native cover class × treatment32851.320.2669
Region12851.430.233
Region × treatment12850.790.3743
Region × native cover class32850.330.8033
Region × native cover class × treatment32852.260.0818
SpringTreatment128310.860.0011
Native cover class32830.360.7832
Native cover class × treatment32831.140.332
Region12834.50.0347
Region × treatment12830.120.7328
Region × native cover class32830.120.9472
Region × native cover class × treatment32830.770.5101
Native forb densityWinterTreatment12850.470.493
Native cover class32850.440.727
Native cover class × treatment32851.090.3529
Region12854.690.0311
Region × treatment12850.140.7105
Region × native cover class32851.40.1583
Region × native cover class × treatment32850.60.6148
SpringTreatment12830.010.9049
Native cover class32831.120.3428
Native cover class × treatment32831.60.1889
Region128312.80.0004
Region × treatment12831.880.1718
Region × native cover class32832.910.0351
Region × native cover class × treatment32831.530.2074
Non-native densityWinterTreatment128519.21<0.0001
Native cover class32852.450.0638
Native cover class × treatment32850.780.5057
Region12850.030.872
Region × treatment12851.090.2967
Region × native cover class32850.310.8198
Region × native cover class × treatment32850.190.903
SpringTreatment128322.66<0.0001
Native cover class32833.730.0118
Native cover class × treatment32831.640.1804
Region12830.050.816
Region × treatment12832.720.1002
Region × native cover class32832.320.0754
Region × native cover class × treatment32830.490.6888
Table 2. Results from repeated measures mixed model ANOVA for native and non-native species richness. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Shaded rows highlight effects that were significant (p < 0.05). Data were sqrt (x + 1)-transformed.
Table 2. Results from repeated measures mixed model ANOVA for native and non-native species richness. Treatment refers to whether plots experienced non-native plant removal (weeded) or not (control). Native cover class refers to the initial range of native cover for the plot (20–29% low, 30–39% medium-low, 40–49% medium-high, 50–59% high). Region refers to whether the restoration site was in the coastal or inland portion of Irvine Ranch Natural Landmarks. Shaded rows highlight effects that were significant (p < 0.05). Data were sqrt (x + 1)-transformed.
Response VariableSeasonEffectNum DFDen DFF Valuep Value
Native species richnessWinterTreatment12850.010.9366
Native cover class32850.110.9551
Native cover class × treatment32852.210.0873
Region12853.180.0756
Region × treatment12851.480.2249
Region × native cover class32850.380.7703
Region × native cover class × treatment32850.490.6927
SpringTreatment12830.380.54
Native cover class32830.330.802
Native cover class × treatment32838.1<0.0001
Region128312.380.0005
Region × treatment12838.020.005
Region × native cover class32831.360.2564
Region × native cover class × treatment32830.180.9104
Non-native species richnessWinterTreatment12854.850.0284
Native cover class32851.50.2148
Native cover class × treatment32850.510.6756
Region12855.20.0233
Region × treatment12851.170.2795
Region × native cover class32850.830.4757
Region × native cover class × treatment32850.550.6478
SpringTreatment12832.910.0893
Native cover class32832.210.0874
Native cover class × treatment32830.090.9638
Region12831.880.172
Region × treatment12830.370.5426
Region × native cover class32832.770.042
Region × native cover class × treatment32831.180.3186
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Ta, P.M.; Griffoul, E.; Sorenson, Q.; Schmidt, K.T.; Ostmann, I.; Huxman, T.E.; Long, J.J.; Balazs, K.R.; Burger, J.C.; Lulow, M.; et al. Effects of Non-Native Annual Plant Removal on Native Species in Mediterranean-Climate Shrub Communities. Diversity 2024, 16, 115. https://doi.org/10.3390/d16020115

AMA Style

Ta PM, Griffoul E, Sorenson Q, Schmidt KT, Ostmann I, Huxman TE, Long JJ, Balazs KR, Burger JC, Lulow M, et al. Effects of Non-Native Annual Plant Removal on Native Species in Mediterranean-Climate Shrub Communities. Diversity. 2024; 16(2):115. https://doi.org/10.3390/d16020115

Chicago/Turabian Style

Ta, Priscilla M., Emily Griffoul, Quinn Sorenson, Katharina T. Schmidt, Isaac Ostmann, Travis E. Huxman, Jennifer J. Long, Kathleen R. Balazs, Jutta C. Burger, Megan Lulow, and et al. 2024. "Effects of Non-Native Annual Plant Removal on Native Species in Mediterranean-Climate Shrub Communities" Diversity 16, no. 2: 115. https://doi.org/10.3390/d16020115

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