Abstract
Non-native species can alter patterns of species diversity at multiple spatial scales, but the processes that underlie multi-scale effects remain unclear. Here we show that non-native species reduce native diversity at multiple scales through simultaneous disruption of two processes of native community assembly: species immigration, which enhances alpha diversity, and community divergence, which enhances beta diversity. Community divergence refers to the process in which local communities diverge over time in species composition because the history of species immigration and, consequently, the way species affect one another within communities are variable among communities. Continuous experimental removal of species over four years of floodplain succession revealed that, when non-native species were excluded, stochastic variation in the timing of a dominant native species’ arrival allowed local communities to diverge, thereby enhancing beta diversity, without compromising promotion of alpha diversity by species immigration. In contrast, when non-native species were allowed to enter experimental plots, they not only reduced native alpha diversity by limiting immigration, but also diminished the dominant native species’ role in enhancing native beta diversity. Our results highlight the importance of community assembly and succession for understanding multi-scale effects of non-native species.
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Introduction
Non-native species are increasingly recognized as a primary cause of the decline of species diversity (Mack et al. 2000; Gaertner et al. 2009; Vilà et al. 2011; Pyšek et al. 2012). Although the presence of non-native species is often correlated with native diversity, the magnitude and direction of this relationship depend on the spatial scale of observation (e.g., Stohlgren et al. 1999, 2002; Fridley et al. 2007; Sandel and Corbin 2010). In other words, native alpha (within-habitat diversity), beta (between-habitat diversity) and gamma (overall diversity integrating alpha and beta) diversities show different relationships with non-native species (e.g., Cleland et al. 2004; Davies et al. 2005). Despite considerable efforts to explain multi-scale effects of non-native species, the paucity of experimental evidence in the plant community assembly literature (Götzenberger et al. 2012) has left it unclear what processes are responsible for these effects and to what extent these apparent effects are actually caused by non-native species per se.
One likely but largely untested explanation for multi-scale effects is that non-native species simultaneously interfere with multiple processes that each promote native diversity, but at different scales. Consider, for example, species immigration as a process that promotes alpha diversity and community divergence as a process that promotes beta diversity. Here we define community divergence as the process in which local communities diverge in species composition for two reasons: (1) communities differ from one another in the history of species immigration and (2) the way species affect one another in a local community depends on immigration history. As local communities assemble, alpha diversity initially increases via species immigration and may remain high if immigration is frequent enough to counter extinction (MacArthur and Wilson 1967). However, given a fixed regional pool of species from which species immigrate, alpha diversity may be inversely related to beta diversity such that high alpha is automatically linked to low beta (Zobel 1997). This relationship arises because the more species local communities contain, the more similar the communities must be in species composition, particularly if local communities are randomly assembled from the regional pool (Koleff et al. 2003; Jost 2007; Vellend et al. 2007). Not all local communities are randomly assembled, however (Götzenberger et al. 2012; Rajaniemi et al. 2012). Some species may modify local habitat conditions upon arrival, and consequently influence the kind of species that can subsequently establish, facilitating some species with certain ecological traits, while inhibiting others with other traits (Weiher and Keddy 1995; Grime 1998; Lepš et al. 2001; Fukami et al. 2005). If so, local communities that vary stochastically in the timing of the arrival of key species can diverge in species composition, resulting in higher beta diversity than expected solely from environmental filtering and otherwise random assembly (Chase 2010). Thus, species immigration and community divergence, when operating concurrently, can dually promote alpha and beta diversity. If this dual promotion is realized in native communities, but disrupted when non-native species invade, this disruption may explain multi-scale effects of non-native species on native diversity. To our knowledge, this possibility has not been tested empirically.
A powerful approach to testing for this possibility would involve continuous removal of multiple species, both native and non-native, to experimentally prevent local establishment of the removed species while otherwise allowing natural community assembly. The effects of the removed species on both alpha and beta diversity can then be evaluated. Few studies have used this type of species removal, however, despite its potential to contribute not just to the basic understanding of non-native species effects, but generally to inform ecosystem restoration efforts (Zavaleta et al. 2001). A handful of recent studies used continuous species removal and yielded new insight into invasion ecology (Hulme and Bremner 2006; Truscott et al. 2008; also see Martin and Wilsey 2012 for a related experiment involving native species addition instead of exotic species removal), but the target of continuous removal in these studies was limited to a single species.
In this paper, we present evidence that non-native species can disrupt both species immigration and community divergence, causing simultaneous reduction in native alpha and beta diversity. The evidence comes from a field study in which we established experimental plots immediately after a major disturbance and then subsequently removed particular sets of plant species (both native and non-native) continuously for 4 years in a highly invaded system in New Zealand (Bellingham et al. 2005; Peltzer et al. 2009). To test for effects of community assembly processes driven by native species and altered by non-native species, we compare native alpha, beta and gamma diversity among plots from which we removed different sets of species in a factorial fashion.
Methods
Study Site
We conducted the experiment on a river floodplain in the Kowhai River Valley, eastern South Island, New Zealand (42º20′ S, 173º33′ E, 220–280 m a.s.l.). The floodplain was sparsely vegetated as a result of flooding. Newly deposited surfaces are very low in nitrogen (N) (Bellingham et al. 2005). A native N-fixing shrub (Coriaria arborea, hereafter Coriaria) and a non-native shrub that does not fix N (Buddleja davidii, hereafter Buddleja) comprised most of the aboveground biomass during the first 10 years of primary succession (Bellingham et al. 2005). The remaining biomass consisted mainly of non-native grasses and herbs, with native woody and herbaceous plants representing only a minor component of the biomass. We previously found that non-native species were characterized by high specific leaf area (SLA), a trait usually correlated positively with relative growth rates and litter decomposition rates (Cornelissen and Thompson 1997; Shipley et al. 2006), relative to native species in this system (Peltzer et al. 2009).
Experimental Design
In January 2002, a major flood completely denuded the floodplain, providing bare surfaces for primary succession to take place (Walker et al. 2006). In April 2002, we randomly located six 50-m transects more than 1 m above water level along a 2-km stretch of the valley (Peltzer et al. 2009). Along each transect, we established eight 1 × 2 m plots spaced 4 m apart, and assigned each plot randomly to one of the following removal treatments: -C-B-E, +C-B-E, -C-B+E, -C+B-E, -C+B+E, +C-B+E, +C+B-E, and +C+B+E, where C = Coriaria, B = Buddleja, E = all non-native species except Buddleja, “+” = retained, and “-” = continuously removed. All native species were retained in all plots (except Coriaria in appropriate plots). As some plots in one transect were lost to disturbance during the experiment, we analyzed data from the other five transects. Our removal treatment involved removing all newly germinated seedlings of the target species from the plots and from a 0.75-m buffer around the perimeter of the plots bimonthly, or ca. every 6 weeks during the growing season, from April 2002 to February 2006. Physical disturbance imposed by the bimonthly removal was minimal: removed biomass never exceeded 0.2 g total dry weight per plot.
Data Collection
Annually, we recorded the presence and cover (using the following cover classes: <1 %, 1–5 %, 6–25 %, 26–50 %, 51–75 %, 76–95 % and >95 %) of all plant species rooted within each plot in December. We then destructively harvested plots in February 2006. To this end, we first trimmed and removed all plant material outside a 0.7 × 1.7 m area centered inside each plot to minimize edge effects. We then collected aboveground biomass for all plant species contained within the 0.7 × 1.7 m area, and determined the dry mass of each species (Peltzer et al. 2009). We also collected fresh foliage of 40 plant species (14 native species and 26 non-native species) to measure foliar N and P concentrations in order to facilitate trait-based interpretation of community divergence (Weiher and Keddy 1995; Shipley et al. 2006; Ackerly and Cornwell 2007). Together, the 40 species comprised >99 % of the total aboveground biomass, and the 14 native species also comprised >99 % of the total native aboveground biomass in the system. We measured total foliar N and P concentrations (%) using automated colorimetric methods (Technicon Instruments 1977). Leaves of each species were sampled from at least 10 individual plants found at the same stage of succession as the experimental plots but located outside the plots.
Diversity Calculation
Using destructive harvest data from February 2006 on the native species for which leaf trait data were available, we calculated alpha, beta and gamma diversity of native plants. Alpha diversity was measured as the number of native species observed per plot. Simpson’s diversity index yielded qualitatively the same results as species richness. Our measure of beta diversity was the dissimilarity of native species composition between plots within treatments, quantified as the mean distance to individual plots from the group centroid, calculated according to the distance matrix based on Jaccard dissimilarity (Anderson 2004, 2006; Anderson et al. 2006). Bray-Curtis dissimilarity, which takes into account species biomass, yielded qualitatively the same results as Jaccard dissimilarity, which considers only the presence and absence of species. Numerous measures of beta diversity have been proposed, each with different strengths and limitations (Koleff et al. 2003; Jost 2007, 2010; Tuomisto 2010; Veech and Crist 2010; Wilsey 2010). We used Anderson’s (2006) measure because it allows between-treatment difference in beta diversity to be statistically tested and is robust and powerful under a variety of conditions (Anderson 2004, 2006; Anderson et al. 2006; Chase 2007, 2010). Gamma diversity was measured as the total number of native species observed in treatments. Although Coriaria is a native species, because it was part of the removal treatments, we excluded it from calculations of native diversity.
Statistical Analysis
In treatment +C-B-E, all native species were allowed to establish, while all non-native species were excluded. We compared this wholly native treatment with other treatments to test for the effects of establishment of Coriaria, Buddleja and other non-native species on native diversity. We examined removal treatment effects using ANOVA followed by Tukey’s HSD test for alpha diversity, using PERMDISP followed by pair-wise a posteriori test (Anderson 2004; Anderson et al. 2006) for beta diversity, and using t-tests (to compare plots where all non-native species were excluded and those where all or some non-native species were retained) for gamma diversity. To ensure our results were not biased by exclusion of rare species, we repeated these analyses using all species recorded in plots instead of including only species for which leaf trait data were available.
It has been pointed out that beta diversity is often not independent of alpha diversity (Koleff et al. 2003; Jost 2007; Vellend et al. 2007). For example, if species are randomly distributed in plots from a common pool of potential colonizers, the smaller the number of species that are distributed per plot (i.e., lower alpha diversity), the more variable the set of species will be between plots (i.e., higher beta diversity). For this reason, in order to compare beta diversity between experimental treatments differing in mean alpha diversity, it is informative to generate a null expectation of beta diversity under different levels of mean alpha diversity, so that observed beta diversity can be examined in light of the null expectation that is corrected for alpha diversity. To this end, we conducted a null model analysis similar to the approach developed by Raup and Crick (1979). Specifically, we first used the data reported in Bellingham et al. (2005: Appendix 2) to estimate the regional frequency of the occurrence of each native species recorded in our experimental plots. The regional frequency of each species was calculated by averaging the observed occurrences of the species across all four developmental stages of the floodplain vegetation (open, young, vigorous and mature stages) identified by Bellingham et al. (2005), taking into account the relative abundance of the developmental stages at the study site. We then generated, for each of the eight experimental treatments, 1,000 sets of null communities by randomly assigning species to plots, with the probabilities of drawing species determined by their regional frequencies estimated as above, while keeping alpha diversity within the experimental treatment the same as observed. Null communities were generated using Mathematica 7.0 (Wolfram Research, Champaign, Illinois, USA). We then used PERMDISP (Anderson 2004) to calculate beta diversity for each set of null communities.
Results
Native Alpha Diversity
When non-native species were prevented from establishing (Fig. 1a), native alpha diversity increased over time as more species arrived. When non-native species were allowed to establish (Fig. 1b), native alpha diversity increased to only about half as much as when non-native species were prevented from establishing. After 4 years of community assembly (Fig. 2a), native alpha diversity was highest when only native species except Coriaria were allowed to establish (treatment -C-B-E). Retaining Coriaria (treatment +C-B-E) did not significantly reduce native alpha diversity from the level of this highest treatment (black bars in Fig. 2a), whereas retaining non-native species often resulted in a significant reduction of native alpha diversity from the level of the highest treatment, particularly in treatment -C-B+E. These results are for the species for which we have leaf trait data, but hold qualitatively when all species recorded are included in the analysis.
Native Beta Diversity
In contrast to results for native alpha diversity, native beta diversity was lowest when only native species except Coriaria were allowed to establish (treatment -C-B-E; Fig. 2b). Retaining Coriaria (treatment +C-B-E) resulted in a significant increase in native beta diversity (Fig. 2b). Retaining non-native species (grey and white bars in Fig. 2b) also increased native beta diversity compared with treatment -C-B-E, but not any more significantly than retaining Coriaria did (treatment +C-B-E; Fig. 2b). As with native alpha diversity, these results for native beta diversity hold qualitatively when all species recorded in plots are included in the analysis.
Native Alpha vs Beta Diversity
Despite these significant differences observed between treatments (Fig. 2 ), native beta diversity was consistently indistinguishable from the null expectation corrected for native alpha diversity in all but one treatment (Fig. 3 ). Only in the wholly native treatment (treatment +C-B-E) did native beta diversity deviate significantly from the null expectation, with the observed value (black circle in Fig. 3 ) significantly higher than expected.
Native Gamma Diversity
Native gamma diversity was higher when non-native species were removed than when all or some non-native species were retained (Fig. 2c).
Non-Native diversity
When non-native species were retained in plots, species removal treatments had no significant effect on alpha, beta or gamma diversity of non-native species (Fig. 4 ).
Coriaria Biomass and Foliar N:P
Coriaria biomass and mean foliar N:P of native plants were significantly correlated when non-native plants were removed (Fig. 5a), whereas no significant relationship was detected when non-native species were retained (Fig. 5b,c,d).
Discussion
Our results provide experimental evidence that non-native species suppressed two diversity-enhancing processes of native community assembly, species immigration and community divergence. To explain this key finding of our study, below we will use our results to argue that, in native community assembly, spatial variation in Coriaria’s time of arrival may have led to variation in the degree of habitat modification by this species, causing different species to establish in different plots according to their ecological traits (Stubbs and Wilson 2004; Holdaway and Sparrow 2006; Wilson and Stubbs 2012) and ultimately increasing beta diversity more than expected from random assembly (Fukami et al. 2005; Lanta and Lepš 2009; Chase 2010). This biotic increase in beta diversity occurred without compromising enhancement of alpha diversity by immigration. We will further argue that non-native species not only reduced native alpha diversity by competitive exclusion, but also diminished Coriaria’s role in enhancing native beta diversity.
Native Alpha Diversity
The high native alpha diversity in the native-species-only treatments (+C-B-E and -C-B-E), in contrast to the low native alpha diversity in the presence of non-native species (Fig. 2a), suggests competitive exclusion of native species by non-native species (Seabloom et al. 2003). Possible mechanisms of competitive exclusion include reduced sites available for germination (Walker et al. 2003) and limiting access to water, nutrients or both (Stubbs and Wilson 2004; Bartelheimer et al. 2010; Everard et al. 2010). The lack of significant reduction of native alpha diversity by Coriaria (Fig. 2a) may seem surprising, given that Coriaria biomass was greater than that of all other species combined. Our previous work suggests, however, that Coriaria is unlikely to negatively affect native alpha diversity even after 30 years of primary succession (Bellingham et al. 2005). If competitive exclusion by Coriaria were to happen over a longer term than our experiment (i.e., >4 yr), our results (Fig. 1 ) suggest that competitive exclusion by non-native species takes place more rapidly (i.e., within 4 years), thereby shortening the time window of enhanced native alpha diversity. Regardless, 4 years of primary succession is a relevant time scale to evaluate community assembly in this system because floods routinely destroy most plant communities on this floodplain every 5–15 years (Bellingham et al. 2005).
Native Beta Diversity
Between the two native-species-only treatments, the higher beta diversity observed in +C-B-E than in -C-B-E (Fig. 2b) may be explained in terms of Coriaria’s potential to modify local nutrient conditions (Walker et al. 2003). As the dominant N-fixer, Coriaria can alleviate the strong N limitation that exists in newly deposited surfaces after a flood (Bellingham et al. 2005). Given variation among plots in the time of Coriaria’s arrival (see variation across x-axis in Fig. 6 ), Coriaria-induced variation among plots in the level of N limitation may have provided opportunities for different sets of species with varying degrees of N demand to establish in different plots. For example, as Coriaria biomass increases, species with higher N:P requirements may become more likely to establish (Güsewell 2004). If Coriaria was continuously prevented from establishing, communities would be predicted to consist of species with lower leaf N:Ps. These communities should also have smaller between-plot variation in foliar N:P than the communities in which Coriaria was allowed to establish. Although the exact mechanisms that control beta diversity remain unknown, we found patterns that are strongly consistent with each of the above predictions regarding Coriaria-driven species sorting according to foliar N:P (Fig. 5a). Moreover, we also found that the time since the first arrival of Coriaria explained most (68 % on average) of the between-plot variation in Coriaria biomass within treatments (Fig. 6 ), suggesting that the main source of variation in Coriaria biomass was indeed the time of their arrival (Bellingham et al. 2005; Walker et al. 2006). If so, the Coriaria-driven assembly of native communities is historically contingent in species taxonomic composition but deterministic in species trait composition (Fukami et al. 2005), a phenomenon that contributes to increased beta diversity (Chase 2010).
Non-native species appear to have disrupted the enhancement of native beta diversity that results from variation in Coriaria immigration, as suggested by the lack of significant relationships between Coriaria biomass and mean foliar N:P of native plants when non-native species were retained (Fig. 5b,c,d). We speculate that, in the native-species-only treatments (Fig. 5a), alleviation of N limitation by Coriaria operated at a highly local scale within plots (i.e., within the rooting zone). We base this speculation on our previous finding that, at the 1 × 2 m plot scale, no significant effect of Coriaria on soil N availability was apparent during 4 years of primary succession in this system (Peltzer et al. 2009). We also know that at a 3 × 3 m plot scale, it takes 10 years or longer for Coriaria’s effect on soil N to emerge (Bellingham et al. 2005). It appears then that Coriaria’s role in enhancing native beta diversity (Figs. 2b, 3) was so local and subtle that it was overruled by competitive exclusion of native species by non-native species. In contrast, neither the diversity (compare grey and white bars in Fig. 4 ) nor the effect on native species diversity (compare grey and white bars in Fig. 2 ) of non-native species was greatly affected by Coriaria. The asymmetrically strong effect of non-native species is surprising because their collective biomass is much less than that of Coriaria (Peltzer et al. 2009), and suggests that subordinate species (sensu Grime 1998) can more strongly control community assembly and diversity than generally thought, likely through rapid tissue turnover and decomposition as inferred from relatively high SLA and foliar N concentrations for non-native species (Peltzer et al. 2009).
Notably, Coriaria was not the only N-fixer in the system, but some non-native species were also N-fixers (e.g., Trifolium and Vicia spp.). Despite their low biomass, non-native N-fixers can add more N to the soil than Coriaria, more likely because of their relatively rapid tissue turnover and decomposition rates, at least at the 1 × 2-m plot scale (Peltzer et al. 2009). Our results for native diversity suggest then that the dual negative effects that non-native species exerted on native alpha and beta diversity overwhelmed any of the potentially positive effects that non-native species may have had on native beta diversity through N addition.
Native Alpha vs Beta Diversity
If non-native species disrupt Coriaria’s role in enhancing native beta diversity (Fig. 5b,c,d), why was native beta diversity high between the plots where non-native species were allowed to establish (grey and white bars in Fig. 2b)? It seems that high native beta diversity in the presence of non-native species is simply a result of statistical inevitability, where low alpha diversity automatically results in high beta diversity (Koleff et al. 2003; Jost 2007; Vellend et al. 2007), as supported by our null model analysis (Fig. 3 ). The wholly native treatment (treatment +C-B-E) was the only exception to the general negative relationship between native alpha and beta diversity: retaining Coriaria appears to have released the native community from the statistical trade-off between alpha and beta diversity, as shown by the significant deviation of beta diversity from expected values (black circle in Fig. 3 ), coupled with increased gamma diversity (Fig. 2c). Taken together, these results suggest that Coriaria drives community divergence, thus increasing beta diversity more than expected from random assembly (Fig. 3 ) despite a high level of alpha diversity maintained by species immigration (Fig. 2a). Importantly, this significant community divergence was realized only when all non-native species were experimentally excluded from plots.
Previously, we showed that co-occuring non-native species in this system had functional traits related to resource acquisition (i.e., high foliar N, high SLA) that differ from co-occruring native species (Peltzer et al. 2009; Kurokawa et al. 2010). Therefore, although we have focused on patterns of diversity in this study, the multi-scale effects of non-native species we have described here may have broader implications for ecosystem functioning, affecting productivity, decomposition, and nutrient cycling (Van der Putten et al. 2000; Lepš et al. 2001).
Conclusion
This study is the first, to our knowledge, to demonstrate that non-native species disrupt multi-scale diversity enhancement by species immigration and community divergence. What made this demonstration possible was the experimental approach involving continuous removal of multiple species. Our findings support the view that the consequences of non-native species invasions for native species diversity can be best understood within the context of biotically driven succession (Rejmánek and Lepš 1996; Meiners et al. 2009; Simberloff 2010; Tognetti et al. 2010). Although this view may seem obviously correct given that most communities are likely in a transient state, rather than in an equilibrium state (Fukami and Nakajima 2011, 2013), relatively little effort has been made to experimentally evaluate non-native species impacts from a succession perspective (Davis et al. 2005). We suggest that applying experimental approaches similar to the one we have used here to a variety of other systems will help to further clarify the importance of community assembly processes for explaining multi-scale effects of non-native species on native diversity.
References
Ackerly DD, Cornwell WK (2007) A trait-based approach to community assembly: partitioning of species trait values into within- and among-community components. Ecol Lett 10:135–145
Anderson MJ (2004) PERMDISP: a FORTRAN computer program for permutational analysis of multivariate dispersions (for any two-factor ANOVA design) using permutation tests. Department of Statistics, University of Auckland, Auckland
Anderson MJ (2006) Distance-based tests for homogeneity of multivariate dispersions. Biometrics 62:245–253
Anderson MJ, Ellingsen KE, McArdle BH (2006) Multivariate dispersion as a measure of beta diversity. Ecol Lett 9:683–693
Bartelheimer M, Gowing D, Silvertown J (2010) Explaining hydrological niches: the decisive role of below-ground competition in two closely related Senecio species. J Ecol 95:126–136
Bellingham PJ, Peltzer DA, Walker LR (2005) Contrasting impacts of a native and an invasive exotic shrub on floodplain succession. J Veg Sci 16:135–142
Chase JM (2007) Drought mediates the importance of stochastic community assembly. Proc Natl Acad Sci USA 104:17430–17434
Chase JM (2010) Stochastic community assembly causes higher biodiversity in more productive environments. Science 328:1388–1391
Cleland EE, Smith MD, Andelman SJ, Bowles C, Carney KM, Horner-Devine MC, Drake JM, Emery SM, Gramling JM, Vandermast DB (2004) Invasion in space and time: non-native species richness and relative abundance respond to interannual variation in productivity and diversity. Ecol Lett 7:947–957
Cornelissen JHC, Thompson K (1997) Functional leaf attributes predict litter decomposition rate in herbaceous plants. New Phytol 135:109–114
Davies KF, Chesson P, Harrison S, Inouye BD, Melbourne BA, Rice, KJ (2005) Spatial heterogeneity explains the scale dependence of the native–exotic diversity relationship. Ecology 86:1602–1610
Davis MA, Pergl J, Truscott AM, Kollmann J, Bakker JP, Domenech R, Prach K, Prieur-Richard AH, Veeneklaas RM, Pyšek P, del Moral R, Hobbs RJ, Collins SL, Pickett STA, Reich PB (2005) Vegetation change: A reunifying concept in plant ecology. Perspect Pl Ecol 7:69–76
Everard K, Seabloom EW, Harpole WS, de Mazancourt C (2010) Plant water use affects competition for nitrogen: why drought factors invasive species in California. Amer Naturalist 175:85–97
Fridley JD, Stachowicz JJ, Naeem S, Sax DF, Seabloom EW. Smith MD, Stohlgren TJ, Tilman D, Von Holle B (2007) The invasion paradox: reconciling pattern and process in species invasions. Ecology 88:3–17
Fukami T, Bezemer TM, Mortimer SR, van der Putten WH (2005) Species divergence and trait convergence in experimental plant community assembly. Ecol Lett 8:1283–1290
Fukami T, Nakajima M (2011) Community assembly: alternative stable states or alternative transient states? Ecol Lett 14:973–984
Fukami T, Nakajima M (2013) Complex plant-soil interactions enhance plant species diversity by delaying community convergence. J Ecol 101:316–324
Gaertner M, Den Breeyen A, Hui C, Richardson DM (2009) Impacts of alien plant invasions on species richness in Mediterranean-type ecosystems: a meta-analysis. Progress in Physical Geography 33:319–338
Götzenberger L, de Bello F, Bråthen KA, Davison J, Dubuis A, Guisan A, Lepš J, Lindborg R, Moora M, Pärtel M, Pellissier L, Pottier J, Vittoz P, Zobel K, Zobel M (2012) Ecological assembly rules in plant communities-approaches, patterns and prospects. Biol Rev 87:111–127
Grime JP (1998) Benefits of plant diversity to ecosystems: immediate, filter and founder effects. J Ecol 86:902–910
Güsewell S (2004) N:P ratios in terrestrial plants: variation and functional significance. New Phytol 164:243–266
Holdaway RJ, Sparrow AD (2006) Assembly rules operating along a primary riverbed–grassland successional sequence. J Ecol 94:1092–1102
Hulme PE, Bremner ET (2006) Assessing the impact of Impatiens glandulifera on riparian habitats: partitioning diversity components following species removal. J Appl Ecol 43:43–50
Jost L (2007) Partitioning diversity into independent alpha and beta components. Ecology 88:2427–2439
Jost L (2010) Independence of alpha and beta diversities. Ecology 91:1969–1974
Koleff P, Gaston KJ, Lennon JJ (2003) Measuring beta diversity for presence-absence data. J Anim Ecol 72:367–382
Kurokawa H, Peltzer DA, Wardle DA (2010) Plant traits, leaf palatability and litter decomposability for co-occurring woody species differing in invasion status and nitrogen fixation ability. Funct Ecol 24:513–523
Lanta V, Lepš J (2009) How does surrounding vegetation affect the course of succession: a five-year container experiment. J Veg Sci 20:686–694
Lepš J, Brown VK, Diaz Len TA, Gormsen D, Hedlund K, Kailová J, Korthals GW, Mortimer SR, Rodriguez-Barrueco C, Roy J, Santa Regina I, Van Dijk C, Van Der Putten WH (2001) Separating the chance effect from other diversity effects in the functioning of plant communities. Oikos 92:123–134
MacArthur RH, Wilson EO (1967) The theory of island biogeography. Princeton University Press, Princeton
Mack RN, Simberloff D, Lonsdale WM, Evans H, Clout M, Bazzaz FA (2000) Biotic invasions: causes, epidemiology, global consequences and control. Ecol Appl 10:689–710
Martin LM, Wilsey BJ (2012) Assembly history alters alpha and beta diversity, exotic–native proportions and functioning of restored prairie plant communities. J Appl Ecol 49:1436–1445
Meiners SJ, Rye TA, Klass JR (2009) On a level field: the utility of studying native and non-native species in successional systems. Appl Veg Sci 12:45–53
Peltzer DA, Bellingham PJ, Kurokawa H, Walker LR, Wardle DA, Yeates GW (2009) Punching above their weight: low-biomass exotic plant species alter soil properties during primary succession. Oikos 118:1001–1014
Pyšek P, Jarošík V, Hulme PE, Pergl J, Hejda M, Schaffner U, Vilà M (2012) A global assessment of invasive plant impacts on resident species, communities and ecosystems: the interaction of impact measures, invading species' traits and environment. Global Change Biol 18:1725–1737
Rajaniemi TK, Goldberg DE, Turkington R, Dyer AR (2012) Local filters limit species diversity, but species pools determine composition. Perspect Pl Ecol 14:373–380
Raup D, Crick RE (1979) Measurement of faunal similarity in paleontology. J Paleontol 53:1213–1227
Rejmánek M, Lepš J (1996) Negative associations can reveal interspecific competition and reversal of competitive hierarchies during succession. Oikos 76:161–168
Sandel B, Corbin JD (2010) Scale, disturbance and productivity control the native–exotic richness relationship. Oikos 119:1281–1290
Seabloom EW, Harpole WS, Reichman OJ, Tilman D (2003) Invasion, competitive dominance and resource use by exotic and native California grassland species. Proc Natl Acad Sci USA 100:13384–13389
Shipley B, Vile D, Garnier E (2006) From plant traits to plant communities: a statistical mechanistic approach to biodiversity. Science 314:812–814
Simberloff D (2010) Invasions of plant communities – more of the same, something very different, or both? Amer Midl Naturalist 163:220–233
Stohlgren TJ, Binkley D, Chong D, Kalkhan MA, Schell LD, Bull KA, Otsuki Y, Newman G, Bashkin M, Son Y (1999) Exotic plant species invade hotspots of native plant diversity. Ecol Monogr 69:25–46
Stohlgren TJ, Chong GW, Schell LD, Rimar KA, Otsuki Y, Lee M, Kalkhan MA, Villa CA (2002) Assessing vulnerability to invasion by non-native plant species at multiple spatial scales. Environm Managem 29:566–577
Stubbs WJ, Wilson JB (2004) Evidence for limiting similarity in a sand dune community. J Ecol 92:557–567
Technicon Instruments (1977) Individual/simultaneous determination of nitrogen and/or phosphorus in BD acid digests. Industrial Methods Number 329-74. Technicon Industrial Systems, Tarrytown
Tognetti PM, Chaneton EJ, Omacini M, Trebino HJ, León RJC (2010) Exotic vs. native plant dominance over 20 years of old-field succession on set-aside farmland in Argentina. Biol Conservation 143:2494–2503
Truscott A-M, Palmer SC, Soulsby C, Westaway S, Hulme PE (2008) Consequences of invasion by the alien plant Mimulus guttatus on the species composition and soil properties of riparian plant communities in Scotland. Perspect Pl Ecol 10:231–240
Tuomisto H (2010) A diversity of beta diversities: straightening up a concept gone awry. Part 1. Defining beta diversity as a function of alpha and gamma diversity. Ecography 33:2–22
Van der Putten WH, Mortimer SR, Hedlund K, Van Dijk C, Brown VK, Lepš J, Rodriguez-Barrueco C, Roy J, Diaz Len TA, Gormsen D, Korthals GW, Lavorel S, Santa Regina I, Šmilauer P (2000) Plant species diversity as a driver of early succession in abandoned fields: a multi-site approach. Oecologia 124:91–99
Veech JA, Crist TO (2010) Toward a unified view of diversity partitioning. Ecology 91:1988–1992
Vellend M, Verheyen K, Flinn KM, Jacquemyn H, Kolb A, Van Calster H, Peterken G, Jessen Graae B, Bellemare J, Honnay O, Brunet J, Wulf M, Gerhardt F, Hermy M (2007) Homogenization of forest plant communities and weakening of species–environment relationships via agricultural land use. J Ecol 95:565–573
Vilà M, Espinar JL, Hejda M, Hulme PE, Jarošík V, Maron JL, Pergl J, Schaffner U, Sun Y, Pyšek P (2011) Ecological impacts of invasive alien plants: a meta-analysis of their effects on species, communities and ecosystems. Ecol Lett 14:702–708
Walker LR, Bellingham PJ, Peltzer DA (2006) Plant characteristics are poor predictors of microsite colonization during the first two years of primary succession. J Veg Sci 17:397–406
Walker LR, Clarkson BD, Silvester WB, Clarkson BR (2003) Colonization dynamics and facilitative impacts of a nitrogen-fixing shrub in primary succession. J Veg Sci 14:277–290
Weiher E, Keddy PA (1995) Assembly rules, null models, and trait dispersion: new questions from old patterns. Oikos 74:159–165
Wilson JB, Stubbs WJ (2012) Evidence for assembly rules: limiting similarity within a saltmarsh. J Ecol 100:210–221
Wilsey BJ (2010) An empirical comparison of beta diversity indices in establishing prairies. Ecology 91:1984–1988
Zavaleta ES, Hobbs RJ, Mooney HA (2001) Viewing invasive species removal in a whole-ecosystem context. Trends Ecol Evol 16:454–459
Zobel M (1997) The relative role of species pools in determining plant species richness: an alternative explanation of species coexistence? Trends Ecol Evol 12:266–269
Acknowledgements
We thank David Wardle for suggestions about experimental design; Bianca Heidecker, Hiroko Kurokawa, Christine Schmidt, David Wardle, and especially Chris Morse for assistance in the field; Mifuyu Nakajima for assistance with null model analysis; Rob Allen, Francesco de Bello, Stan Harpole, Matt Knope, Tadashi Miyashita, members of the community ecology group at Stanford University, and several anonymous reviewers for comments; the New Zealand Department of Conservation for access to study sites; and the Core funding for Crown Research Institutes from the New Zealand Ministry of Business, Innovation and Employment’s Science and Innovation Group. We wish to dedicate this paper to Professor Jan Lepš to acknowledge his distinguished contribution to plant ecology.
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Fukami, T., Bellingham, P.J., Peltzer, D.A. et al. Non-Native Plants Disrupt Dual Promotion of Native Alpha and Beta Diversity. Folia Geobot 48, 319–333 (2013). https://doi.org/10.1007/s12224-013-9175-z
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DOI: https://doi.org/10.1007/s12224-013-9175-z