*Correspondence and present address. Friday Harbor Laboratories, University of Washington, 620 University Road, Friday Harbor, WA 98250, USA. E-mail: firstname.lastname@example.org
1Invading species typically need to overcome multiple limiting factors simultaneously in order to become established, and understanding how such factors interact to regulate the invasion process remains a major challenge in ecology.
2We used the invasion of marine algal communities by the seaweed Sargassum muticum as a study system to experimentally investigate the independent and interactive effects of disturbance and propagule pressure in the short term. Based on our experimental results, we parameterized an integrodifference equation model, which we used to examine how disturbances created by different benthic herbivores influence the longer term invasion success of S. muticum.
3Our experimental results demonstrate that in this system neither disturbance nor propagule input alone was sufficient to maximize invasion success. Rather, the interaction between these processes was critical for understanding how the S. muticum invasion is regulated in the short term.
4The model showed that both the size and spatial arrangement of herbivore disturbances had a major impact on how disturbance facilitated the invasion, by jointly determining how much space-limitation was alleviated and how readily disturbed areas could be reached by dispersing propagules.
5Synthesis. Both the short-term experiment and the long-term model show that S. muticum invasion success is co-regulated by disturbance and propagule pressure. Our results underscore the importance of considering interactive effects when making predictions about invasion success.
Biological invasions are a global problem with substantial economic (Pimentel et al. 2005) and ecological (Mack et al. 2000) costs. Research on invasions has provided important insights into the establishment, spread and impact of non-native species. One key goal of invasion biology has been to identify the factors that determine whether an invasion will be successful (Williamson 1996). Accordingly, ecologists have identified several individual factors (e.g. disturbance and propagule pressure) that appear to exert strong controlling influences on the invasion process. However, understanding how these processes interact to regulate invasions remains a major challenge in ecology (D’Antonio et al. 2001; Lockwood et al. 2005; Von Holle & Simberloff 2005).
In order for any invasion to be successful, propagule arrival must coincide with the availability of resources needed by the invading species (Davis et al. 2000). Therefore, the interaction between propagule pressure and processes that influence resource availability will ultimately determine invasion success (Brown & Peet 2003; Lockwood et al. 2005; Buckley et al. 2007). In this study we used the invasion of shallow, subtidal kelp communities in Washington State by the Japanese seaweed Sargassum muticum as a study system to better understand the effects of propagule pressure and disturbance on invasion. In a factorial field experiment we manipulated both propagule pressure and disturbance in order to examine how these factors independently and interactively influence S. muticum establishment in the short term. We supplement the experimental results with a parameterized integrodifference equation model, which we use to examine how different natural disturbance agents influence the spread of S. muticum through the habitat in the longer term. Although a successful invasion clearly requires both establishment and spread of the invader, most studies have looked at just one of these processes (Melbourne et al. 2007). We take an integrative approach by employing both a short-term experiment and a longer-term model, allowing us to examine the effects of disturbance and propagule limitation on the entire invasion process.
Our field research was based out of Friday Harbor Laboratories on San Juan Island, Washington State, USA. The field experiment was carried out at a site within the San Juan Islands Marine Preserve network adjacent to Shaw Island, known locally as Point George (48.5549° N, 122.9810° W). Field work was accomplished using SCUBA in shallow subtidal communities.
The native algal community characteristic of sheltered, rocky subtidal habitats in this region is species-rich and structurally complex (see Britton-Simmons 2006 for a more detailed description). In this ecosystem, space is an important limiting resource and in the absence of disturbance there is little or no bare rock available for newly arriving organisms to colonize. This habitat has a diverse fauna of benthic herbivores, including molluscs and sea urchins, that create disturbances by clearing algae from the rocky substrata. The green sea urchin Strongylocentrotus droebachiensis is a generalist herbivore that reduces the abundance of native algae and creates relatively large disturbed patches (Vadas 1968; Duggins 1980). In the shallow zone where S. muticum is found, the green urchin is highly mobile and often occurs in aggregations (Paine & Vadas 1969; Foreman 1977; Duggins 1983; personal observation). Green urchins avoid areas where S. muticum is present because it is not a preferred food resource (Britton-Simmons 2004), but they can be found feeding in uninvaded areas adjacent to existing S. muticum populations (personal observation). Green urchins therefore create intermittent but relatively intense disturbances in areas where S. muticum is absent and some proportion of these disturbances can potentially be exploited by dispersing S. muticum propagules. In contrast, herbivorous benthic molluscs (chitons, limpets and snails) are ubiquitous in the shallow subtidal and unlike sea urchins they are unaffected by the presence of S. muticum (Britton-Simmons 2004). Herbivory by individual molluscs creates relatively small-scale disturbances, thereby providing a consistent supply of microsites that can be colonized by newly arriving species, including Sargassum muticum (see Appendix S1 in Supplementary Material for more information about mollusc diets).
Sargassum muticum is a brown alga in the order Fucales that was introduced to Washington State in the early 20th century, probably with shipments of Japanese oysters that were imported for aquaculture beginning in 1902 (Scagel 1956). It is now common in shallow subtidal habitats throughout Puget Sound and the San Juan Islands (Nearshore Habitat Program 2001, personal observation). In the San Juan Islands, S. muticum has a pseudoperennial life history. Each holdfast produces as many as 18 laterals in the early spring, each of which can grow as tall as three metres. In late summer to early autumn the laterals senesce and are lost, leaving only the basal holdfast portion of the thallus to overwinter.
Sargassum muticum has a diplontic (uniphasic) life cycle, is monecious, and is capable of selfing. Reproduction typically occurs between late June and late August in our region. During reproduction the eggs of S. muticum are released from and subsequently adhere to the outside of small reproductive structures called receptacles. Once fertilized, the resulting embryos remain attached while they develop into tiny germlings (< 200 µm in length) with adhesive rhizoids (Deysher & Norton 1982). Germlings then detach from the receptacle and sink relatively quickly, recruiting in close proximity to the parent plant (Deysher & Norton 1982). Although most recruitment occurs within 5 m of adult plants, recruits have been found as far as 30 m from the nearest adult (Deysher & Norton 1982). Longer distance dispersal probably occurs when plants get detached from the substratum and subsequently become fertile after drifting for some period of time (Deysher & Norton 1982). One distinctive feature of the S. muticum invasion is that it is extremely limited in vertical extent. In the San Juan Islands, S. muticum is found from the low intertidal to the shallow subtidal zone (Norton 1977; personal observation), from approximately –0.5 m Mean Lower Low Water (MLLW) to –7 m MLLW. However, it is most abundant in the shallow subtidal, from approximately –2 m MLLW to –4 m MLLW. Thus, in areas where S. muticum has invaded it forms a narrow band along the shore.
We used a two-way factorial design manipulating propagule pressure (six levels) and disturbance (two levels) with three replicates per treatment combination. Subtidal plots (30 cm × 30 cm) at a depth of 3–4 m below MLLW were selected so that differences in the identity and abundance of taxa, aspect, and relief were minimized and the plots were randomly assigned to treatments. None of the experimental plots contained S. muticum prior to the experiment. However, some S. muticum was present at Point George and it was removed prior to the reproductive season in order to prevent contamination of the experimental plots from external sources of S. muticum propagules.
The disturbance treatment had two levels: control and disturbed. Control plots were not altered in any way, but they did vary somewhat in how much natural disturbance had occurred in them prior to the experiment (mean = 7.7% of plot area). Plots in the disturbance treatment were scraped down to bare rock so that no visible organisms remained. These two treatments represent extremes in the levels of disturbance that are likely to occur in nature. The unaltered control plots contained a rich assemblage of native species. The disturbed plots were similar in spatial scale to a patch that a small group of urchins might create, but represent an unusually intense disturbance because all native species, including crustose coralline algae (which cover an average of 27.7% of the substratum at this depth), were removed. These treatments maximized our ability to detect an effect of disturbance in our experiment.
Immediately following the imposition of the disturbance treatment (July 2002) the plots were experimentally invaded by suspending ‘brooding’S. muticum over them. This was accomplished by collecting S. muticum from the field and transporting them to the lab where the appropriate ratio of sterile to reproductive tissue (see below) was placed in 30 cm × 30 cm vexar bags. The bags were returned to the field the same day and suspended over the experimental plots for 1 week. Propagule pressure was manipulated by varying the ratio of sterile to reproductive tissue in the bags while holding the total biomass of S. muticum tissue constant. The propagule pressure treatment had six levels, corresponding to the following amounts of reproductive tissue (in grams): 0, 50, 100, 175, 250 and 350 (average mass of mature S. muticum in this region is 174 g). Based on propagule production–mass relationships derived by Norton & Deysher (1988) for S. muticum, we estimate that approximately 5 million propagules were released in each replicate of our highest propagule pressure treatment. We assumed a linear relationship between the mass of adult reproductive tissue and propagule output because we know of no Sargassum study that suggests otherwise. Sterile tissue was added to bags as necessary in order to bring the total biomass to 350 g. Reproductive and sterile tissue was mixed in the bags so that the reproductive tissue was well distributed throughout. This experimental manipulation mimics the level of propagule input that would occur in an incipient invasion or if a drifting plant became tangled with attached algae and subsequently released its propagules.
Recruitment of S. muticum was quantified by counting the number of S. muticum juveniles that were present in the plots 5 months after the experimental invasion, which is the earliest they can reliably be seen in the field. We resurveyed the plots to count the number of S. muticum adults present 11 months after the invasion (just prior to reproductive season) and then removed all S. muticum from the experimental plots in order to prevent it from spreading.
We analysed the S. muticum recruitment data using a two-way anova followed by separate regression analyses on each disturbance treatment. For the control treatment, we performed a multiple regression to determine what proportion of recruitment variation was explained by propagule input and space availability. For the disturbed plots, which did not vary in the amount of available space, we carried out a simple linear regression to determine the impact of propagule input on recruitment. We used the results of these analyses to inform the construction of mechanistic candidate functions for the relationship between propagule input, space availability and recruitment. These candidate functions were compared using differences in the Akaike's information criteria (AIC differences; Burnham & Anderson 2002). We then used model averaging, a form of multimodel inference in which parameter estimates from more than one candidate function are used jointly to describe the data, in order to select a parameterized recruitment function for the S. muticum spread model.
The S. muticum survivorship data did not conform to the assumptions of anova (even after a number of different transformations) so we used a non-parametric Kruskal–Wallis test to ask whether S. muticum survivorship differed in the disturbed and control treatments. We then fitted five different survivorship functions, assuming binomial error, to the data to test whether S. muticum survivorship (number of adults per recruit) was density-dependent. Because the Kruskal–Wallis test suggested that survivorship differed significantly between the two disturbance treatments (see Results) we chose to fit the models to those two treatments separately to test for density dependence. In addition to type 1 (linear), type 2 (saturating), and type 3 (sigmoidal) functions, we also fitted a constant survivorship model. These candidate functions were compared using the Akaike's information criterion (AIC differences; Burnham & Anderson 2002).
The numbers of adult S. muticum (after 11 months) also violated the assumptions of anova (despite transformations), so we used non-parametric statistics to test two hypotheses: (i) adult density is independent of disturbance treatment (Wilcoxon Signed Ranks Test), and (ii) adult density is independent of propagule pressure treatment (Kruskal–Wallis Test).
We used an integrodifference equation (IDE) model to describe the spatial spread of an S. muticum population. IDE models assume that the habitat is continuous in space, and that reproduction and dispersal occur in discrete bouts. The depths inhabited by S. muticum comprise a relatively narrow vertical band, so the spread of the population was assumed to occur in a one-dimensional habitat. The model follows two state variables through time. Nt(x) is the density of S. muticum at a location x along this habitat at time t, and Zt(x) is the amount of bare rock at x during t. The values for these state variables are determined by functions representing the important ecological processes in this system. Sargassum muticum density is determined by the production and recruitment of propagules and by adult survival. Bare rock is created by benthic herbivore disturbances, since herbivores consume native algae and thus alleviate space limitation. The form of our model is then
Nt+1(x) = sPt(x)f(Pt(x),Zt(x)) + rNt(x),eqn 1
Zt+1(x) = (1 - ht(x))gZt(x) + ht(x)A.eqn 2
Pt(x) is the number of propagules at location x at the start of year t, and equals the number of propagules produced at x and remaining near their parent plant plus the sum of propagules from all other locations within the habitat (with endpoints a and b) which disperse to x. Pt(x) is governed by the equation Each adult produces ω propagules and their dispersal is described by the function k. The function f(Pt(x), Zt(x)) in equation 1 gives the fraction of propagules which successfully recruit, given that the amount of bare rock at location x equals Zt(x) and there is an initial input of Pt(x) propagules. Based on data from the experiment, we assume that recruitment function has the form f(Pt(x),Zt(x)) =ρ1(Zt(x) + ρ2)ρ5Pt(x)/[1 + ρ3(Zt(x) + ρ2)ρ5 + ρ4Pt(x)2], with values for the ρi and methods for fitting this function given in Appendix S2. s and r are fractions of germlings and adults, respectively, that survive to the following year. Parameters for Sargassum fecundity and dispersal were attained from the literature (Deysher & Norton 1982; Norton & Deysher 1988) and all other parameter values used in our simulations were estimated from our own field data. The methods and results for fitting parameters are given in Appendix S2.
In equation 2, ηt(x) is the proportion of the habitat scraped clear by grazers. If left ungrazed, we assumed that bare rock at a given location experiences geometric decay, with rate g, as it becomes utilized by native algae. The parameter A in equation 2 is a scaling constant representing the size of the habitable area at each point x. We modelled benthic herbivore disturbance in two different ways. First, we constructed a stochastic model for ηt(x) based on our understanding of the natural history of the system. Second, we built a more generalized stochastic model for ηt(x). In the S. muticum system, bare rock is generated in small patches when an area is grazed by molluscs (chitons and limpets), or in larger patches by sea urchin grazing. Both types of disturbance create bare rock for S. muticum to potentially exploit, and the disturbance types differ only in their size and spatial distribution. We assumed that the mollusc disturbances are ubiquitous, whereas large urchin-grazed areas are patchily distributed across the habitat. Due to uncertainty in the exact size and frequency of these disturbances, we ran simulations over a very wide range of possible parameter values. In the generalized model for ηt(x), we allowed disturbances of any size to occur with any degree of spatial aggregation, rather than requiring large disturbances to be patchy and small ones to be spread throughout the habitat. Our methods for drawing values for ηt(x) in these simulations are described in Appendix S3 and summarized in Table C.1 therein.
In our system, native benthic grazers do not eat S. muticum adults (Britton-Simmons 2004; personal observation), but it is unknown whether they will consume new S. muticum recruits when they are very small (e.g. Sjøtun et al. 2007) and hence difficult to avoid ingesting incidentally. Whether or not disturbance events can directly cause mortality of the invader can be very important in determining invasion success (Buckley et al. 2007). In our simulations, we therefore considered both the case where S. muticum is never eaten by grazers, and the case where S. muticum is eaten at the rate ηt(x) until it reaches the age of 1 year.
The field experiment showed that recruitment of S. muticum was higher in plots that were disturbed compared to control plots (Fig. 1a) suggesting that resource availability limited recruitment. Increasing propagule pressure led to significant increases in average S. muticum recruitment in both disturbance treatments (Fig. 1a). Finally, a significant interaction between disturbance and propagule pressure (F5,24 = 3.77, P = 0.01) indicates that the plots in the two disturbance treatments differed in the extent to which they were limited by propagule availability. Multiple regression analysis of the S. muticum recruitment data from the control treatment, with space and propagule input as continuous explanatory variables, explained most of the recruitment variability (R2 = 0.87, Fig. 1a). This analysis showed that both space (Fig. 1a, b = 0.703, P < 10−4) and propagule treatment (Fig. 1a, b = 0.657, P < 10−3) had strong influences on recruitment in the control treatment. Because there was no variation in space availability in the disturbed treatment, we used simple linear regression analysis to examine the relationship between propagule input and S. muticum recruitment in the disturbed treatment (Fig. 1a, R2 = 0.84, P < 10−6). The results suggest that in the absence of space limitation propagule input explains most of the variability in S. muticum recruitment.
We used these results to create a set of mechanistic candidate functions for the relationship between S. muticum recruitment, propagule pressure and space availability (see Appendix S2). The only candidate models supported by the data (AIC differences < 4; Burnham & Anderson 2002) show a type 3 (sigmoidal) relationship between propagule pressure and recruitment, and either a type 2 (saturating) or type 3 relationship between available space and recruitment (Appendix S2, Table B.1). Due to practical constraints on the number of treatments that could be replicated in the field, we have data only on very low available space (control plots) and very high available space (disturbed plots), and insufficient data at intermediate values to resolve the functional relationship between space-limitation and recruitment. We therefore used model averaging (Burnham & Anderson 2002) to combine our parameter estimates for the two supported models and used the resulting function to describe space- and propagule-limitation in recruitment in the simulation model. We also ran simulations using each of the supported recruitment models separately. The results from the two supported models and the averaged model were very similar, so we present results only from the averaged model.
Survivorship (from 5 months to 11 months of age) of S. muticum was significantly higher in disturbed plots (U = 76.5, P < 0.05). Mean survivorship (± 1 SD) in control plots was 3.4% (± 3.8%), compared to 6.1% (± 2.2%) in disturbed plots. Our analysis of survivorship as a function of recruitment density suggests density-independence (Appendix S2, Table B.2), so we used the mean survivorship across all experimental plots as the germling survival rate (s) in our model.
Simulations of the parameterized model under various disturbance regimes reveal several interesting patterns. Using the disturbance scenario with ubiquitous mollusc disturbances and large, patchily distributed urchin disturbances, we found that a single adult S. muticum was almost always sufficient to start a successful invasion. This is in agreement with our empirical observation that propagule input always resulted in positive recruitment, even in space-poor control plots. We quantified population growth in our model by reporting the density of S. muticum after 100 years, averaged across the invaded area, and we use the length of habitat occupied by S. muticum after 100 years as a measure of invasion rate. When we assumed that S. muticum was never consumed by benthic herbivores, both the mean S. muticum population density and the length of the invaded area increased with both the mean intensity of mollusc grazing and with the size and number of urchin disturbances (Fig. 2, solid lines). Changing the variance in the intensity of mollusc grazing had essentially no effect (not shown). Unless urchin disturbances were extremely large and numerous (top 3 lines, Fig. 2g–j), the mollusc grazing had a much stronger effect on S. muticum density than did urchin grazing.
When we assumed that native grazers eat S. muticum germlings, S. muticum density and the length of habitat invaded still increased with the intensity of mollusc disturbance, as long as molluscs grazed less than 50% of the habitat bare (Fig. 2, dashed lines). Actual mollusc disturbances are typically much smaller than 50% (personal observation). Indeed, we note that if all of the bare rock in the experiment's control plots was attributed to mollusc grazing, the average grazing intensity would be only 7.7%. Within the realistic range of parameter values, then, molluscs facilitate the invasion in the model even when they consume young S. muticum.
Urchin disturbances that were few and/or small had little effect on the invasion, but large and numerous urchin disturbances decreased the final S. muticum density and the size of the invaded area when grazers consumed new recruits (Fig. 2e–j). Sargassum muticum failed to establish when urchin disturbances were both very large (20–50 m of linear habitat scraped bare per disturbance) and extremely abundant (100–200 such disturbances per year). These results are corroborated by the generalized model of disturbance, which showed that when the total proportion of the habitat disturbed per year is held constant smaller disturbances affecting a greater number of locations resulted in the highest final S. muticum densities and invaded areas (Appendix S2, Fig. C.1). When these disturbed locations were more clumped in space, this resulted in a slight decrease in the final size of the invaded area.
The treatment effects were still apparent when adults were counted at the end of the experiment (Fig. 1b). Adult S. muticum density was higher in the disturbed treatment than in the control treatment (Z = –3.41, P < 0.001). In addition, adult S. muticum density appeared to be positively related to propagule pressure (Fig. 1b, H5 = 16.10, P = 0.006), with high propagule pressure resulting in a maximum of between 20 and 25 adults per plot (900 cm2).
How was the probability of successful invasion influenced by propagule pressure? We defined successful invasion of an experimental plot as the presence of one or more adult S. muticum at the end of the experiment (11 months after invasion). We consider this a reasonable way to define invasion success given that reproduction of these adults was imminent (< 1 month away), survivorship is very high at this life-history stage (Appendix S2, Table B.3), and both our model and experimental results indicate that a single individual is capable of establishing a population. We plotted the proportion of plots in each treatment combination that were successfully invaded as a function of propagule pressure (Fig. 3). Because we had only three replicates per treatment combination the probability values were constrained to four possible values (0, 0.33, 0.66, or 1.0). In addition, we tested only six levels of propagule input and therefore have limited capacity to resolve the details of this relationship. Therefore, we did not attempt to fit statistical models to these data. In disturbed plots, invasion was certain even at the lowest level of propagule pressure in our experiment (Fig. 3). However, in control plots the probability of invasion was less than 1 until propagule pressure reached a level of 250 g of reproductive tissue, an amount of tissue greater than the average mass of an adult S. muticum (Fig. 3).
Our experimental results demonstrate that space- and propagule-limitation both regulate S. muticum recruitment. Our finding that S. muticum recruitment was positively related to propagule input is similar to those of two previous studies (Parker 2001; Thomsen et al. 2006), in which the propagule input of invasive plants was manipulated. In our control treatment space was limiting, a result that has also been found in previous studies of S. muticum recruitment (Deysher & Norton 1982; De Wreede 1983; Sanchez & Fernandez 2006). Consequently, increasing propagule pressure had a relatively weak effect on recruitment in undisturbed plots (Fig. 1a). However, when space limitation was alleviated by disturbing the plots, increasing propagule pressure caused a dramatic increase in recruitment (Fig. 1a). This suggests that in the presence of adequate substratum for settlement, propagule limitation becomes the primary factor controlling S. muticum recruitment. These results indicate that S. muticum recruitment under natural field conditions will be determined by the interaction between disturbance and propagule input.
Only a few previous studies have investigated the effect of resource supply on the relationship between propagule pressure and recruitment of an introduced species. Although disturbance generally increases invasion success by increasing resource availability (Richardson & Bond 1991; Bergelson et al. 1993; Levin et al. 2002; Valentine & Johnson 2003; Clark & Johnston 2005), Parker (2001) found evidence that disturbance reduced Scotch broom (Cystisus scoparius) recruitment from seed at all levels of propagule input. This effect occurred because the native flora actually facilitated Scotch broom germination, probably by increasing soil moisture and/or nutrients (Parker 2001). Similarly, Thomsen et al. (2006) showed that in the absence of a water addition treatment establishment of an exotic perennial grass was greatly reduced, even at high levels of propagule input. Finally, Valentine & Johnson (2003) found that disturbance facilitated invasion by the introduced kelp Undaria pinnatifida even when propagule pressure was high. These studies and our own work provide empirical evidence that the interaction between propagule input and the biotic and abiotic processes that mediate resource availability will be key to understanding patterns of invasion.
The effects of the disturbance and propagule pressure treatments that were manifest in the S. muticum recruitment data persisted until the end of the experiment (Fig. 1b). That adult S. muticum density was higher in the disturbed treatment than in the control treatment suggests that disturbance may increase the population growth rate of S. muticum during the initial stages of the invasion. Natural disturbances that are less intense than our experimental scrapings might have a more modest effect on S. muticum density, but our simulation results suggest that even small disturbances can play a major role in facilitating the invasion. Our simulations further suggest that this effect should persist over long time-scales (Fig. 2).
In subtidal habitats both biotic and abiotic disturbances occur, but it is doubtful that they are both relevant to the S. muticum invasion in this system. Consumption of algae by the diverse fauna of benthic herbivores in this system (see Methods) is a common and consistent source of disturbance that is likely to be relevant to the S. muticum invasion and was therefore the focus of our model. Abiotic disturbances are unlikely to play an important role in this regard because tidal currents are not a substantial cause of algal mortality in this region (Duggins et al. 2003) and the inland waters of Puget Sound, the San Juan Islands and the Strait of Georgia are protected from the ocean swells that play a key role on the outer coast of Washington State. Although locally generated storm waves are an important source of disturbance during the winter (Duggins et al. 2003), storms during the summer months when S. muticum is reproductive are rare.
simulated urchin/mollusc disturbances
In addition to enhancing S. muticum recruitment, disturbance increased the survivorship of juvenile S. muticum. In our system, the green urchin (Strongylocentrotus droebachiensis) creates relatively large disturbed patches and S. muticum that recruit to these patches probably benefit from reduced competition with native algae. Unlike other systems where sea urchins feed on both native and non-native algae alike (Valentine & Johnson 2005), green urchins do not consume adult S. muticum (Britton-Simmons 2004) although it is possible that they incidentally consume new recruits. Studies in other systems have also reported positive effects of disturbance on the survivorship of non-native species (Gentle & Duggin 1997; Williamson & Harrison 2002). In general, disturbance probably enhances survivorship because it reduces the size or abundance of native species that compete for resources with invaders (Gentle & Duggin 1997; Britton-Simmons 2006). Indeed, our modelling results suggest that even when juvenile survivorship is reduced by herbivory, the net effect of grazers is still usually positive (Fig. 2).
The simulation model suggested that not all disturbance agents have equivalent effects on space-limitation. Small bare patches throughout the habitat facilitated S. muticum spread (Fig. 2 and Appendix S3, Fig. C.1) by increasing the amount of bare rock near any given reproductive adult. Molluscs are ubiquitous in these subtidal habitats and although they typically create very small disturbances, the model suggests that this is sufficient for S. muticum to successfully invade, even in the absence of other disturbance agents (e.g. urchins and humans).
Urchins create much larger open spaces, but urchin disturbances could not be used by settling propagules unless a reproductive adult happened to be nearby or a long-distance dispersal event occurred. When there are many urchin disturbances in a year, the chance that such a disturbance occurs near an S. muticum adult increases and, because long-distance propagule dispersal is rare, this greatly enhances the likelihood that a propagule will reach the disturbed area. Accordingly, small numbers of urchin disturbances in our model did not affect the spread of S. muticum (Fig. 2a–d), but numerous and sufficiently large disturbances did (Fig. 2e–j). Washington State is at the southern end of the green urchin's range in the eastern Pacific and at the majority of sites in the San Juan Islands this species is absent or at relatively low abundance. Consequently, molluscs are probably the most important source of disturbance for S. muticum in this region; green urchins may be a more important disturbance agent in more northerly portions of its range (where it reaches higher densities). That urchin disturbance was not necessary for successful invasion by S. muticum in the model is an important result because S. muticum has invaded many areas in this region where urchins are absent. Indeed, urchins avoid areas where S. muticum is present (Britton-Simmons 2004) and since this effect was not included in the model, urchin disturbances probably contribute even less to S. muticum spread than our simulations suggest.
propagule pressure and invasion success
How much invasion risk does a given level of propagule pressure pose? Previous studies have demonstrated a positive relationship between propagule pressure and the establishment success of non-native species (Grevstad 1999; Parker 2001; Ahlroth et al. 2003; Cassey et al. 2005). However, we know very little about the relationship between establishment probability and propagule pressure or the factors that affect it (Lockwood et al. 2005). Possibilities include a linear relationship (Lockwood et al. 2005) as well as more complex relationships containing thresholds or other non-linearities (Griffith et al. 1989; Ruiz & Carlton 2003; Lockwood et al. 2005; Buckley et al. 2007). Our experimental results suggest that the relationship is non-linear (Fig. 3). Indeed, all communities in which abiotic factors do not preclude invasion are probably vulnerable to invasion such that above some threshold level of propagule input successful invasion is a virtual certainty. Consequently, this relationship must be nonlinear because by definition it saturates at a probability of one. In our system disturbance appeared to reduce the level of propagule pressure necessary to ensure invasion success. However, even control plots had a high probability of invasion once the level of propagule pressure exceeded that produced by an average adult S. muticum. Unfortunately, the limited number of treatment levels in our experiment constrains our ability to resolve the details of this relationship. Nevertheless, in the control treatment there was some evidence of a threshold level of propagule pressure below which invasion was very unlikely to occur (Fig. 3).
Our model reflects what we believe to be the most important factors limiting invasion success (propagule-limitation and competition for space) but other factors we did not include in the model, such as stochastic mortality, density-dependent mortality of adults, competition with native species for resources besides space (e.g. light, Britton-Simmons 2006) and abiotic conditions, could constrain S. muticum's distribution and abundance in the field. Empirical studies have demonstrated the importance of biotic resistance in regulating invasions (see reviews by Levine & D’Antonio 1999; Levine et al. 2004) and the community that S. muticum is invading is no exception (Britton-Simmons 2006). However, some authors have suggested that propagule pressure has the potential to overcome biotic resistance (D’Antonio et al. 2001; Lockwood et al. 2005). Levine (2000) found that seed supply overpowered biotic resistance that was generated by plant communities at small spatial scales (18 cm × 18 cm). A more recent terrestrial experiment also reported that propagule pressure was the primary determinant of invasion success, overwhelming the effects of other factors, such as disturbance and resident diversity, which were concurrently manipulated (Von Holle & Simberloff 2005). However, ‘propagules’ in that study were seedlings transplanted into experimental plots and seedlings may not be regulated by the same factors as seeds, which are the life stage responsible for invasion spread in natural systems. Nevertheless, if propagule pressure can indeed overcome those factors that were not included in our model then one might ask why S. muticum has not completely taken over the shallow subtidal zone in this system, as our model predicts under most disturbance regimes. Interestingly, whether S. muticum is indeed in the process of doing so is not entirely clear. There are very few areas in the San Juan region where S. muticum is completely absent at the appropriate depths (personal observation), yet at many sites S. muticum is currently at low abundance and it is unclear whether these sites represent incipient invasions or whether something is inhibiting local population growth.
In our system, neither disturbance nor propagule input alone was sufficient to maximize invasion success (i.e. establishment probability and invader population density). Increasing propagule pressure had relatively little effect on total recruitment in control plots (Fig. 1a), though at high levels it ultimately overcame space limitation and ensured successful invasion (Fig. 3). However, even at high levels of propagule input, final S. muticum density was low in the absence of disturbance (Fig. 1b). Based on our experimental results alone, we might have predicted strong effects of both molluscs and urchins on the S. muticum invasion in the long term. However, the simulation model suggested that these two natural disturbance agents should have different effects on long-term invasion due to differences in the spatial structure of these disturbances. The model results demonstrate that caution should be exercised when extrapolating the results of short-term disturbance experiments over longer time intervals. In this marine community invasion success was co-regulated by propagule pressure and biotic resistance. Our results underscore the importance of considering interactive effects when making predictions about invasion success.
Thanks to Ben Pister, Sam Sublett and Jake Gregg for SCUBA assistance in the field. For helpful discussions that improved this work we thank Timothy Wootton, Cathy Pfister, Greg Dwyer, Joy Bergelson, Mathew Leibold, Spencer Hall and Bret Elderd. Yvonne Buckley, Barney Davies and an anonymous referee provided very helpful comments on an earlier version of the manuscript. The director and staff of Friday Harbor Laboratories provided logistical support and access to laboratory and SCUBA facilities. The field research was funded by a grant to Timothy Wootton from The SeaDoc Society at UC Davis, and both authors were supported by a Graduate Assistance in Areas of National Need Training Grant (P200A040070) during the completion of this work.