Contemporary connectivity is sustained by wind- and current-driven seed dispersal among seagrass meadows
© Ruiz-Montoya et al.; licensee BioMed Central. 2015
Received: 17 December 2014
Accepted: 26 February 2015
Published: 2 April 2015
Seagrasses are clonal marine plants that form important biotic habitats in many tropical and temperate coastal ecosystems. While there is a reasonable understanding of the dynamics of asexual (vegetative) growth in seagrasses, sexual reproduction and the dispersal pathways of the seeds remain poorly studied. Here we address the potential for a predominantly clonal seagrass, P. australis, to disperse over long distances by movement of floating fruit via wind and surface currents within the coastal waters of Perth, Western Australia. We first simulated the dominant atmospheric and ocean forcing conditions that are known to disperse these seagrass seeds using a three-dimensional numerical ocean circulation model. Field observations obtained at 8 sites across the study area were used to validate the model performance over ~2 months in summer when buoyant P. australis fruit are released into the water column. P. australis fruit dispersal trajectories were then quantified throughout the region by incorporating key physical properties of the fruit within the transport model. The time taken for the floating fruit to release their seed (dehiscence) was incorporated into the model based on laboratory measurements, and was used to predict the settlement probability distributions across the model domain.
The results revealed that high rates of local and regional demographic connectivity among P. australis meadows are achieved via contemporary seed dispersal. Dispersal of seeds via floating fruit has the potential to regularly connect meadows at distances of 10s of kilometres (50% of seeds produced) and infrequently for meadows at distances 100 s km (3% of seeds produced).
The spatial patterns of seed dispersal were heavily influenced by atmospheric and oceanographic conditions, which generally drove a northward pattern of connectivity on a regional scale, but with geographical barriers influencing finer-scale connectivity pathways at some locations. Such levels of seed dispersal infer greater levels of ecological and genetic connectivity and suggest that seagrasses are not just strongly clonal.
KeywordsCoastal circulation Dispersal Population connectivity Posidonia australis Seagrasses
Quantifying population connectivity within coastal ecosystems is a crucial component of the management and conservation of many marine populations, especially when it becomes necessary to forecast how increasing environmental pressures such as water quality degradation, species invasions and climate change will impact these ecosystems . In order to accurately assess marine connectivity, it is imperative to understand the dominant physical transport processes in a region (e.g., tides, waves, wind, etc.) and how the biological dispersal capabilities of different species interact with these physical dynamics. It is ultimately these biophysical interactions that determine how the spatial connectivity pathways of marine populations are influenced over a broad range of spatial scales, depending on transport mechanisms that are present, as well as the physical characteristics of the propagule that is being dispersed [2-4].
Seagrasses are marine plants with the ability to reproduce both asexually (clonally) and sexually (via seeds). There is a reasonable understanding of the dynamics of asexual seagrass reproduction that has led to the development of meadow expansion models based on rates of linear growth [5,6], nonlinear models of seagrass growth [7,8] and even three-dimensional (3D) models of structural formation of meadows (e.g. ). Conversely, sexual reproduction, seed dispersal and recruitment in seagrasses remain much more poorly studied . Seed dispersal is the process governed by the movement from the initial release of a fruit by the parent plant to the time when the seed settles to a location where it may recruit. This trajectory is affected by different physical and biological components (see Levin et al.  for a general review of seed dispersal). In the coastal and estuarine environments that seagrasses inhabit, flow generated by currents and waves generate bed shear stresses capable of transporting seeds in the bottom boundary layer [4,12,13]. However, the positively buoyant fruit of some seagrass species are transported at the air-water interface by surface ocean currents as well as direct wind forces, which can provide a mechanism for long distance dispersal [10,14-16]. Ultimately these seeds must also settle in favourable substrata and in suitable environmental conditions for recruitment to be successful .
For seagrasses, most attempts to quantify dispersal distances have tended to be only very crude estimates, e.g., as derived from rough (order-of-magnitude) measures of background ocean currents and seed lifecycle characteristics, or inferred from genetics . Kendrick et al.  emphasised the wide ranges of dispersal distances that have been reported for different seagrass species. Dispersal distance estimates vary from only a few meters for the negatively buoyant seeds of Zostera marina when on the sediment surface , to hundreds of kilometres in studies of the fruit of Thalassia obtained by a genetic metapopulation study  and estimates of surface travel of Enhalus and Thalassia fruit by extreme events (e.g., typhoons) [15,16]. Despite the importance of dispersal to demographic connectivity in seagrasses, there are still major gaps in our understanding of the spatial implications of the connectivity of distant populations and the importance of locally- versus regionally-derived recruitment processes on individual populations . To develop a predictive understanding of demographic connectivity in seagrasses, we thus need to know: 1) seed production estimates and the rate at which these propagules are released from the parent plant, 2) the physical vector responsible for dispersal or where these seeds are transported to and over what time scale, and 3) the survival rates of seeds once they settle. We can estimate seed production (e.g. [19,20]), investigate germination and survival rates under controlled conditions (e.g. [21-23]) and sometimes even observe natural recruitment [15,24,25]. However, for the most part we still do not know where seeds are ultimately transported to in most seagrass ecosystems, and hence where new recruits that may structure seagrass populations originate from.
The use of process-based models that incorporate both predictions of the key hydrodynamic transport mechanisms as well as the physical characteristics of seeds and fruit have the capability to advance our understanding of dispersal pathways in complex coastal systems . This approach has only been used for seagrasses in a very limited number of studies, focusing on dispersal of the European populations of Zostera marina. Källström et al.,  empirically estimated a maximum dispersal distance of ~150 km from wind fields acting on rafting shoots bearing seeds. However, wind was the only forcing mechanism considered in the model and hence no hydrodynamic information was incorporated. Erftemeijer et al.,  used a 3D ocean model to simulate the trajectories of Z. marina shoots released inside a large estuary and predicted dispersal distances of up to 130 km over a 3–4 week period. However, transport was due to the surface currents but there was no data to accurately account for additional transport from windage. In general, this class of particle tracking modelling has proven to be successful for predicting the transport of seagrass shoots, fish larvae (e.g. [28,29]) and corals , although the accuracy is dependent on how well the properties of the dispersing propagule are known. Ruiz-Montoya et al.,  have already described how dispersal propagules of P. australis move under different wind and current forcing, forming the basis for parameterizing our modelling of seed dispersal in this study.
The southwest region of Australia has one of the highest diversities of temperate seagrasses in the world throughout a 2500 km coastline . The dominant genera in the region are Posidonia and Amphibolis, and they create large mono-specific meadows with smaller species as understorey [31,32]. The fruit of P. australis are released during the austral summer (November-December), and because these fruit are less dense than seawater, they rapidly float to the water surface where they are transported by ocean surface currents and wind drag (‘windage’) acting on their air exposed surface. This flotation period lasts until dehiscence (seed release) occurs, which can take up to ~5 days . After dehiscence, the negatively buoyant seed settles at ~10 cm s−1 and once it reaches the seafloor, requires shear stresses greater than ~100 mPa to be moved. This energy is not likely to be reached by unidirectional currents in the region (e.g. due to wind and tide), but oscillatory wave-driven flows may further mobilize the seeds over short distances, especially during storm conditions .
In this study we hypothesize that Posidonia australis populations throughout the south-western margin of Australia have a potential for high contemporary connectivity over large distances due to their floating fruit. We investigate this potential connectivity by modelling the two-dimensional dispersal patterns of P. australis fruit in the coastal waters of Perth, Western Australia, driven by a combination of transport by modelled ocean surface currents as well as direct windage.
Hydrodynamic model performance
Model Skill computed via Eq. ( 1 ) for the subtidal depth-averaged currents, subtidal surface currents and water levels
Depth- averaged (east)
Depth- averaged (north)
Depth- averaged speed
Statistics of the dispersal distances predicted from the model with (left) and without windage (right)
Dynamics driving dispersal
Within our study area, dispersal distances were greater for offshore meadows, as the fruit were able to be transported in the stronger ocean currents located offshore and were also less likely to be deposited on land when winds switched onshore during the afternoon. Although a northward gradient of potential connectivity is evident, especially when taking into account LDD, within sheltered sites the dispersal processes were heavily influenced by the local hydrodynamics. These fine-scale circulation patterns caused some sites to have a dominant southward transport that opposed the northward wind stresses. This reflects the importance of local water circulation within nearby meadows in the region, which may also influence finer-scale population genetic structure . Coastal landmasses also restricted connectivity among meadows when they affected northward transport; thus, these populations might present differences in terms of shared genotypes, resulting in a subpopulation structure when isolated from the dominant northward transport. Other external factors known to influence dispersal in seagrasses are extreme events such as storms and hurricanes (e.g. [16,37]). Locally, storms typically occur during the winter and lead to strong winds; whereas summer conditions are relatively calmer but with more consistent wind forcing. Therefore, storm effects are not likely to influence average dispersal distance for P. australis in this region. However, remote tropical storms as far as ~1000 km from the study area can generate large coastal trapped waves [35,38], which can episodically lead to large cross- and along-shore flows that may also contribute to seed dispersal along this coast.
Long distance dispersal
This study demonstrates that fruit dispersal in the seagrass Posidonia australis is a regional phenomenon. Every year seeds have the capacity to be transported over distances ranging from metres to 100 km or more, supporting the suggestion that in some species of seagrasses, seagrass populations living within these distances should have high demographic connectivity . Dispersal is an essential process in plant population dynamics, where heavy investment in different seed characteristics has improved adaptation to different dispersing agents . In terrestrial environments, this has resulted in specialized mechanisms that are known to efficiently disperse seeds over different spatial scales, depending on the seed characteristics and on the dispersing agents such as wind, water and different animal species (see ). These strategies in terrestrial plants have historically been fairly well-studied, although these have mainly focused on average dispersal distances that only imply a typical dispersal scale of a population . A great effort is being put into elucidating long distance dispersal (LDD), connectivity and metapopulation ranges for terrestrial angiosperms (see  and references within), which ultimately relates to a population’s survival and evolution [43-45].
The atmospheric and oceanographic conditions in the region result in northward LDD for P. australis of at least ~100 km from individual reproductive events. So despite the low probability for reaching these distances, the abundant production of seeds is likely to provide enough recruits to make this an important event over multiple years. This result highlights the importance of reproduction and LDD for this seagrass as well as other seagrasses with floating fruits or propagules . Our estimates of LDD are similar to other seagrass species such as Zostera marina that have suggested a dispersal potential of ~100-150 km on rafting shoots bearing seeds (see [26,27]).
On the western coastline of Australia, the climatic and oceanographic context results in a northward trajectory of long distance dispersal. This dependence on wind-generated currents, direct windage, and the location of coastal landmasses that act as barriers to fruit movement, determines contemporary or demographic connectivity and presumably the evolutionary connectivity of populations of Posidonia australis. Our simulations suggest important probabilities (~40%) of ‘local’ connectivity (1–15 km) between adjacent meadows, as a result of the exponential decay in the probability of fruit dehiscence over time. This level of dispersal and population connectivity is supported by population genetic evidence (see ) that found chaotic genetic patchiness, evidence of active sexually derived recruits, high genetic diversity in local populations and some shared multi-locus genotypes over distances of 8 to 12 kilometres, at the same locations we have modelled. Our results are also supported by observations from other seagrasses. For example, in the tropical seagrass species (Thalassia testudinum), Van Dijk et al.  estimated dispersal from extrapolation of velocities of tracked floating fruit and inferred distances of up to ~350 km. Their results were also supported by genetic metapopulation distances in the same order . Collectively, these results acknowledge the importance of long distance dispersal to the regional dynamics of seagrass populations with floating fruit or propagules.
There was substantial contemporary dispersal among most populations in this study, clearly suggesting a high level of demographic connectivity among these populations, although this connectivity was generally highly directional towards the north. The exception is the offshore site at Rottnest Island (R_PP), located in a bay protected from the west and facing land to the north. Therefore, this sheltered site acted largely as a sink, opposite to the rest of the sites, as most of the fruit are either self-recruited or entirely lost from the domain; however, there is still some small likelihood that this site receives seeds from most of the southern release sites. Interestingly, this site could present high genetic diversity acquired through a very slow recruiting process from many of the surrounding sites. Successful recruitment from seed dispersal increases gene flow among populations, resulting in greater diversity within local populations, which can also confer resilience to disturbances . Also, high diversity is especially important for threatened ecosystems as it improves adaptation to changing environmental conditions . The ability of marine angiosperms to reproduce vegetatively at high rates, originally led to the idea that seagrasses very seldom recruited from seed. However, observations of greater expansion of meadows than expected from measured clonal growth (e.g. ), the high numbers of seeds produced (e.g. ), occasional observed recruited seedlings (e.g. [25,51]) and large genetically related metapopulations with high genetic diversity within and among populations (e.g. [52,53]), all suggest that successful seed dispersal events are not rare and continuously contribute to seagrass populations of P. australis in southwest Australia.
This exercise allowed us to gain new insight into the range of dispersal that Posidonia australis seeds likely experience and thus a more complete picture of connectivity among local populations. Despite every effort put into modelling the dispersal of the fruit as accurate as possible based on the known biology and the physical processes, the size of model domain (~100 km) still constrained estimates of the actual maximum long distance dispersal distances, given that a small percentage of particles left the northern boundary. Thus, even for this relatively large model domain, the connectivity of these local seagrass populations with regions extending further to the north of the study area remains unknown. In addition, our simulations were run for the summer of 2010, and although the general patterns of dispersal are expected to be very similar during other years, the strength of the Leeuwin Current does display some inter-annual variability (i.e. due to the El Niño - La Niña cycle) , and hence the overall dispersal distances could vary slightly between years. As with every modelling simulation, there is also always scope to include additional processes, and while we are quite confident that the results of this buoyant transport phase are realistic, for future work we would like to incorporate secondary transport of the seeds at a finer resolution to better understand the dynamics that directly affect post settlement. This study presents the first estimates of local population connectivity through sexual reproduction; however, it does not account for successful recruitment into the reproductive adult population. Further research is also needed to better understand the factors that contribute to successful recruitment in the region, which would provide a comprehensive picture of the full life cycle of this important seagrass species, from reproduction, to seed dispersal, to recruitment, and finally to the successful establishment of new meadows.
Population dynamics in seagrasses result from a complex balance between vegetative expansion and seed recruitment. Our capacity to infer population dynamics through sexual recruitment depends on our ability to first understand dispersal. In this study we show the strong influence of local wind over the movement of P. australis floating fruit. Additionally, this coupling with regional to fine scale hydrodynamic processes highlights the importance of local circulation in places where complex water transport is present, such as very shallow coastal areas or semi-enclosed embayments. For surface driven transport, dispersal distances on the order of a few km’s to ~100 km or more are generally predicted, with large distances reached over exposed areas with directionally defined flows. These distances are likely to result in a well-connected south to north corridor along the dominant direction of dispersal. Ultimately an understanding of the dispersal process together with the conditions that favor recruitment and seedling survival can provide us with better strategies to understand and manage these threatened ecosystems.
Hydrodynamic model setup
A numerical circulation model MIKE3  was used to solve the 3D incompressible Reynolds averaged Navier–Stokes equations and was applied to simulate the circulation dynamics in the coastal waters of Perth, Western Australia. The model domain extended ~100 km along the coast with the northern boundary located near Two Rocks (−31.49° S), the southern boundary near Mandurah (−32.53° S), and the western boundary located roughly 40 km offshore where the depth reached just over 100 m (Figure 1a). The size of the domain was chosen as the maximum area allowed by our computational power without compromising resolution for the small scale processes. The study region also included three major islands: Rottnest, Garden and Carnac. This model domain was gridded with an unstructured triangular mesh (~50000 elements), with the grid resolution increasing roughly proportional to the local depth in order to keep the local barotropic Courant numbers less than 0.8 for the typical barotropic time step (~20 s) used in the simulations. The typical (average) grid cell resolution was thus ~140 m in shallow coastal areas (depths <20 m). In the vertical, 10 sigma (terrain-following) layers were used and were distributed uniformly throughout the water column.
A series of hindcast simulations were conducted to validate the hydrodynamic model predictions, which focused specifically on a ~2 month period during the austral summer (November-December) when the fruits of Posidonia in Perth’s coastal waters are released  and when hydrodynamic data from an extensive field experiment in the region were also available . In this experiment, currents were measured at 8 stations throughout the study area (Figure 1a) and included 5 acoustic Doppler current profilers (ADCPs) that recorded current profiles at the deeper sites (>10 m) and 3 acoustic Doppler velocimeters (ADVs) that recorded currents at a fixed height above the bed at the shallow inshore sites [for details of the instruments and their configurations refer to 35]. We note that the results from this experiment showed that the circulation on both the inner shelf and the Perth coastal lagoon region further inshore (depths <100 m) were not significantly influenced by local stratification (i.e. buoyancy forcing contributions to the circulation were negligible); as a result, density gradients were ignored in the model configuration.
The three open boundaries were forced using a linear interpolation of hourly water levels predicted by the Global Tide Model Data based on TOPEX/POSEIDON altimetry . The water level boundary conditions were also modified to include the typical magnitude of the southward-directed alongshore pressure gradient of 2x10−7 m that drives the offshore Leeuwin Current following Godfrey and Ridgway  and Smith et al. . Surface wind forcing in the model was based on observations recorded at a local weather station (available every minute from Rottnest Island near the centre of the model domain) by the Bureau of Meteorology and was applied uniformly across the domain using surface drag coefficients from Smith and Banke . The bottom stresses were computed in the model assuming a logarithmic profile in the bottom boundary layer with a hydraulic bottom roughness length scale of z o = 0.01 m (the appropriateness of this roughness value was also investigated by initially conducting a series of sensitivity tests of the influence of bottom roughness on the model results – see below). Horizontal diffusion of momentum was modelled using a Smagorinsky formulation with an eddy viscosity of 0.55 m2 s−1 and a k-ε turbulence closure scheme in the vertical. Finally, Coriolis forcing was included in the model and allowed to spatially vary across the domain. The reader is encouraged to see the software log for one of these simulations presented as an Additional file 1.
where X represents the variable to be analysed, either as predicted by the model (X model) or the observations (X obs), and where the overbars denote time-averaged values. For Eq. (1), perfect model-data agreement thus results in value of one whereas a value of zero implies complete disagreement. The Skill was computed at each of the observation sites and was applied by separately comparing both the depth-averaged flows (U d ,V d ), as well as the surface flows (U s ,V s ) at the deeper sites (Figure 1a). We note that we focus on evaluating the performance of the model to predict the subtidal component of the circulation since this had by far the greatest influence on the net transport of seeds fruit the five day dehiscence wind period. Given the weak oscillatory tidal currents in Perth’s coastal waters , the maximum tidal excursion lengths are typically <500 m. Nevertheless, in all of the particle dispersal simulations, tidal currents were still included. In addition, water levels computed from the ADCP and ADV bottom-mounted pressure sensors corrected for local atmospheric pressure, were also compared to the model output. To assess the current variability at each site, for both the field data and model predictions, a principal component analysis was performed on the variance of the easterly (U) and northerly (V) velocity components . The time series of both the observed and modelled currents were then rotated into the major and minor axes of the variance; in most cases these defined the alongshore and cross-shore flow directions, respectively (see below).
Fruit particle tracking (dispersal and connectivity simulations)
Output from the hydrodynamic transport model was used to drive a Lagrangian particle tracking model that advected particles with the fruit characteristics and simulated dispersal as a random walk process. In the random walk, horizontal dispersion coefficients were based on a scaled horizontal eddy viscosity from the Smagorinsky formulation (a typical value of 0.01 was used for the scaling factor, although the results were advection-dominated and negligibly influenced when this parameter was varied over more than an order of magnitude). For this application the dispersal of P. australis floating fruit were treated as passive particles transported at the sea surface. In addition to the transport of particles by the ocean surface current vectors from the hydrodynamic model, the additional transport by windage on the floating P. australis fruit, as detailed in Ruiz-Montoya et al. , were included in the model. The windage consisted of 1.2% of the local wind speed and was added to the surface transport, which was based on field studies of the response of tracked P. australis fruit to different wind forcing conditions (refer to ). These coupled hydrodynamic-particle tracking simulations focused specifically on the period from the 24th of November to the 15th December 2010, when local P. australis fruit were observed to be released in the coastal waters of Perth (see the Additional file 1 for the model settings). Fruit release in the region occurs annually and the environmental regime is quite consistent with easterly winds during the morning and strong seabreezes in the afternoon [35,61]. The transport of fruit was assessed from fourteen meadows chosen for fruit release (Figure 1b). These sites spanned the full study area; however there were more sites within Cockburn Sound, firstly because these populations are among the best mapped along Perth , and secondly because most of these sites coincided with genetic sampling studies by Sinclair et al. [46,63] that can be utilised in future work. Each release site consisted of 30 by 30 m zones over which the seagrass fruit were randomly released. Twenty five particles per site were released every hour during the study period (~12,500 per site), which is likely an under estimate of the seeds produced and released in these areas by a factor of ~4 (M. Waycott, personal communication). This maximum number of simulated particles was based on the computational limitations of the particle tracking; however, they will have a negligible influence on the actual probability distributions of dispersal that are the focus here. Each particle (fruit) was allowed to travel for up to 5 days (based on results from ). Any particles that left the model domain during this period were recorded as lost; however an extrapolation on the velocity of the last 12 hours before leaving the domain was applied for the remaining time until final dehiscence, to investigate LDD potential. From Ruiz-Montoya et al.  where ~1200 fruit were monitored, the percent of remaining (non-dehisced) fruit were empirically fit to y = a exp(−bt), where t represents time in days, y the dehiscence percentage of the studied sample, which gave a = 117 and b = 0.78 d−1 (see ). This expression represents an exponential distribution of a continuous random variable; hence its probability density function (PDF) of dehiscence was defined as P (t) = 0.781exp(−0.781t). After each particle tracking simulation, the individual particle trajectories were analysed based on their positions every second hour. Using the dehiscence probability P (t) curve, the settlement locations of individual seeds were then recorded. Horizontal transport during the rapid settlement phase was not incorporated, due to the fast settling velocity of P. australis seeds; for example, a transport of only 15 m would result in a maximum depth of 20 m from a current speed of 0.075 m s−1, which is considered relatively fast in the study area (see ). The probabilities for settlement were then spatially assigned among a 500 m × 500 m grid of the entire study area, thereby producing a settlement probability map. This process was carried out for the 14 different release sites. Finally, this information was used to quantify the connectivity between the different sample sites by computing a connectivity matrix for the region, where the rows represent the meadow receiving the seed and intersect columns that represent the meadow sourcing the fruit .
We would like to thank the reviewers and editor, whose comments allowed us to present this text in a clearer manner. The offshore current data was obtained from the Integrated Marine Observing System (IMOS) (www.imos.org.au). We would also like to thank the Bureau of Meteorology and the Department of Transport for providing the wind and water level data. This research was funded by a University of Western Australia Research Development Award and an Australian Research Council Future Fellowship grant (FT110100201) to RJL, as well as Australian Research Council Linkage Project grants to GAK (LP100200429), and GAK and RJL (LP130100918).
- Cowen RK, Sponaugle S. Larval dispersal and marine population connectivity. In: Annual review of marine science, vol. 1. 2009. p. 443–66. Annual Review of Marine Science.Google Scholar
- Siegel DA, Kinlan BP, Gaylord B, Gaines SD. Lagrangian descriptions of marine larval dispersion. Mar Ecol Prog Ser. 2003;260:83–96.View ArticleGoogle Scholar
- Gaylord B, Reed DC, Raimondi PT, Washburn L. Macroalgal spore dispersal in coastal environments: mechanistic insights revealed by theory and experiment. Ecol Monogr. 2006;76:481–502.View ArticleGoogle Scholar
- Ruiz-Montoya L, Lowe RJ, Van Niel KP, Kendrick GA. The role of hydrodynamics on seed dispersal in seagrasses. Limnol Oceanogr. 2012;57:1257–65.View ArticleGoogle Scholar
- Kendrick GA, Eckersley J, Walker DI. Landscape-scale changes in seagrass distribution over time: a case study from Success Bank, Western Australia. Aquat Bot. 1999;65:293–309.View ArticleGoogle Scholar
- Marbà N, Duarte CM. Rhizome elongation and seagrass clonal growth. Mar Ecol Prog Ser. 1998;174:269–80.View ArticleGoogle Scholar
- Sintes T, Marbà N, Duarte CM. Modeling nonlinear seagrass clonal growth: assessing the efficiency of space occupation across the seagrass flora. Estuar Coasts. 2006;29:72.View ArticleGoogle Scholar
- Sintes T, Marbà N, Duarte MC, Kendrick GA. Nonlinear processes in seagrass colonisation explained by simple clonal growth rules. Oikos. 2005;108:165–75.View ArticleGoogle Scholar
- Kendrick GA, Marbà N, Duarte CM. Modelling formation of complex topography by the seagrass Posidonia oceanica. Estuar Coast Shelf Sci. 2005;65:717–25.View ArticleGoogle Scholar
- Kendrick GA, Waycott M, Carruthers TJB, Marion LC, Hovey R, Krauss SL, et al. The central role of dispersal in the maintenance and persistence of seagrass populations. Bioscience. 2012;62:56–65.View ArticleGoogle Scholar
- Levin SA, Muller-Landau HC, Nathan R, Chave J. The ecology and evolution of seed dispersal: a theoretical perspective. Annu Rev Ecol Evol Syst. 2003;34:575–604.View ArticleGoogle Scholar
- Koch EW, Ailstock MS, Booth DM, Shafer DJ, Magoun AD. The role of currents and waves in the dispersal of submersed angiosperm seeds and seedlings. Restor Ecol. 2010;18:584–95.View ArticleGoogle Scholar
- Orth RJ, Luckenbach M, Moore KA. Seed dispersal in a marine macrophyte - implications for colonization and restoration. Ecology. 1994;75:1927–39.View ArticleGoogle Scholar
- Clarke PJ, Kerrigan RA, Westphal CJ. Dispersal potential and early growth in 14 tropical mangroves: do early life history traits correlate with patterns of adult distribution? J Ecol. 2001;89:648–59.View ArticleGoogle Scholar
- Harwell MC, Orth RJ. Long-distance dispersal potential in a marine macrophyte. Ecology. 2002;83:3319–30.View ArticleGoogle Scholar
- Lacap CDA, Vermaat JE, Rollon RN, Nacorda HM. Propagule dispersal of the SE Asian seagrasses Enhalus acoroides and Thalassia hemprichii. Marine Ecol-Progress Series. 2002;235:75–80.View ArticleGoogle Scholar
- McMahon K, van Dijk K-j, Ruiz-Montoya L, Kendrick GA, Krauss SL, Waycott M, et al. The movement ecology of seagrasses. Proc R Soc B Biol Sci. 2014. doi: 10.1098/rspb.2014.0878.Google Scholar
- van Dijk JK, van Tussenbroek BI, Jiménez-Durán K, Márquez-Guzmán GJ, Ouborg J. High levels of gene flow and low population genetic structure related to high dispersal potential of a tropical marine angiosperm. Mar Ecol Prog Ser. 2009;390:67–77.View ArticleGoogle Scholar
- Conacher CA, Poiner IR, O’Donohue M. Morphology, flowering and seed production of Zostera capricorni Aschers in subtropical Australia. Aquat Bot. 1994;49:33–46.View ArticleGoogle Scholar
- Terrados J. Sexual reproduction and seed banks of Cymodocea nodosa (Ucria) Ascherson meadows on the southeast Mediterranean coast of Spain. Aquat Bot. 1993;46:293–9.View ArticleGoogle Scholar
- Kuo J, Kirkman H. Fruits, seeds and germination in the seagrass Halophila-ovalis (Hydrocharitaceae). Bot Mar. 1992;35:197–204.View ArticleGoogle Scholar
- Brenchley JL, Probert RJ. Seed germination responses to some environmental factors in the seagrass Zostera capricorni from eastern Australia. Aquat Bot. 1998;62:177–88.View ArticleGoogle Scholar
- Belzunce M, Navarro RM, Rapoport HF. Posidonia oceanica seeds from drift origin: viability, germination and early plantlet development. Bot Mar. 2008;51:1–9.View ArticleGoogle Scholar
- Olesen B, Marba N, Duarte CM, Savela RS, Fortes MD. Recolonization dynamics in a mixed seagrass meadow: the role of clonal versus sexual processes. Estuaries. 2004;27:770–80.View ArticleGoogle Scholar
- Balestri E, Lardicci C. First evidence of a massive recruitment event in Posidonia oceanica: spatial variation in first-year seedling abundance on a heterogeneous substrate. Estuar Coast Shelf Sci. 2008;76:634–41.View ArticleGoogle Scholar
- Källström B, Nyqvist A, Åberg P, Bodin M, André C. Seed rafting as a dispersal strategy for eelgrass (Zostera marina). Aquat Bot. 2008;88:148–53.View ArticleGoogle Scholar
- Erftemeijer PLA, van Beek JKL, Ochieng CA, Jager Z, Los HJ. Eelgrass seed dispersal via floating generative shoots in the Dutch Wadden Sea: a model approach. Mar Ecol Prog Ser. 2008;358:115–24.View ArticleGoogle Scholar
- Kim S, Barth J. Connectivity and larval dispersal along the Oregon coast estimated by numerical simulations. J Geophysical Res. 2011. doi: 10.1029/2010JC006741.Google Scholar
- Chiswell SM, Rickard GJ. Larval connectivity of harbours via ocean currents: a New Zealand study. Cont Shelf Res. 2011;31:1057–74.View ArticleGoogle Scholar
- Condie SA, Andrewartha JR. Circulation and connectivity on the Australian North West Shelf. Cont Shelf Res. 2008;28:1724–39.View ArticleGoogle Scholar
- Carruthers TJB, Dennison WC, Kendrick GA, Waycott M, Walker DI, Cambridge ML. Seagrasses of south-west Australia: a conceptual synthesis of the world’s most diverse and extensive seagrass meadows. J Exp Mar Biol Ecol. 2007;350:21–45.View ArticleGoogle Scholar
- Kendrick GA, Holmes KW, Van Niel KP. Multi-scale spatial patterns of three seagrass species with different growth dynamics. Ecography. 2008;31:191–200.View ArticleGoogle Scholar
- Cresswell G. The Leeuwin current near Rottnest Island, Western Australia. Marine Freshwater Res. 1996;47:483.View ArticleGoogle Scholar
- Feng M, Meyers G, Pearce A, Wijffels S. Annual and interannual variations of the Leeuwin Current at 32 degrees S. J Geophysical Res-Oceans 2003. doi: 10.1029/2002jc001763.Google Scholar
- Ruiz-Montoya L, Lowe RJ. Summer circulation dynamics within the Perth coastal waters of southwestern Australia. Cont Shelf Res. 2014;77:81–95.View ArticleGoogle Scholar
- White C, Selkoe KA, Watson J, Siegel DA, Zacherl DC, Toonen RJ. Ocean currents help explain population genetic structure. Proc R Soc B Biol Sci. 2010;277:1685–94.View ArticleGoogle Scholar
- Bell SS, Fonseca MS, Kenworthy WJ. Dynamics of a subtropical seagrass landscape: links between disturbance and mobile seed banks. Landsc Ecol. 2008;23:67–74.View ArticleGoogle Scholar
- Eliot M, Pattiaratchi P. Remote forcing of water levels by tropical cyclones in southwest Australia. Cont Shelf Res. 2010;30:1549.View ArticleGoogle Scholar
- Howe H, Miriti M. When seed dispersal matters. Bioscience. 2004;54:651–60.View ArticleGoogle Scholar
- Hughes L, Dunlop M. Predicting dispersal spectra: a minimal set of hypotheses based on plant attributes. J Ecol. 1994;82:933.View ArticleGoogle Scholar
- Nathan R. Long-distance dispersal of plants. Science. 2006;313:786–8.View ArticleGoogle Scholar
- Kremer A, Ronce O, Robledo-Arnuncio JJ, Guillaume F, Bohrer G, Nathan R, et al. Long-distance gene flow and adaptation of forest trees to rapid climate change. Ecol Lett. 2012;15:378–92.View ArticleGoogle Scholar
- Nathan R, Muller-Landau HC. Spatial patterns of seed dispersal, their determinants and consequences for recruitment. Trends Ecol Evol. 2000;15:278–85.View ArticleGoogle Scholar
- Nathan R. Long-distance dispersal research: building a network of yellow brick roads. Divers Distrib. 2005;11:125–30.View ArticleGoogle Scholar
- Trakhtenbrot A, Nathan R, Perry G, Richardson DM. The importance of long-distance dispersal in biodiversity conservation. Divers Distrib. 2005;11:173–81.View ArticleGoogle Scholar
- Sinclair E, Krauss S, Anthony J, Hovey R, Kendrick G. The interaction of environment and genetic diversity within meadows of the seagrass Posidonia australis (Posidoniaceae). Mar Ecol Prog Ser. 2014;506:87–98.View ArticleGoogle Scholar
- Hughes AR, Inouye BD, Johnson MTJ, Underwood N, Vellend M. Ecological consequences of genetic diversity. Ecol Lett. 2008;11:609–23.View ArticleGoogle Scholar
- Reusch TBH, Ehlers A, Hammerli A, Worm B. Ecosystem recovery after climatic extremes enhanced by genotypic diversity. Proc Natl Acad Sci U S A. 2005;102:2826–31.View ArticleGoogle Scholar
- Kendrick GA, Hegge BJ, Wyllie A, Davidson A, Lord DA. Changes in seagrass cover on success and Parmelia Banks, Western Australia between 1965 and 1995. Estuar Coast Shelf Sci. 2000;50:341–53.View ArticleGoogle Scholar
- Orth RJ, Harwell MC, Inglis GJ. Ecology of seagrass seeds and dispersal strategies. In: Larkum AWD, Robert JO, Duarte CM, editors. Seagrasses: biology, ecology and conservation. Netherlands: Springer; 2006. p. 111–33.Google Scholar
- Rivers DO, Kendrick GA, Walker DI. Microsites play an important role for seedling survival in the seagrass Amphibolis antarctica. J Exp Mar Biol Ecol. 2011;401:29–35.View ArticleGoogle Scholar
- Jover MA, del Castillo-Agudo L, Garcia-Carrascosa M, Segura J. Random amplified polymorphic DNA assessment of diversity in western Mediterranean populations of the seagrass Posidonia oceanica. Am J Bot. 2003;90:364–9.View ArticleGoogle Scholar
- Bricker E, Waycott M, Calladine A, Zieman JC. High connectivity across environmental gradients and implications for phenotypic plasticity in a marine plant. Marine Ecol-Progress Series. 2011;423:57–67.View ArticleGoogle Scholar
- DHI. MIKE 21 & MIKE 3 flow model, hydrodynamic and transport module, scientific documentation. Hørsholm, Denmark: DHI Water Environment Health; 2010.Google Scholar
- Andersen OB. Global ocean tides from ERS 1 and TOPEX/POSEIDON altimetry. J Geophys Res. 1995;100:25249.View ArticleGoogle Scholar
- Godfrey JS, Ridgway KR. The large-scale environment of the Poleward-Flowing Leeuwin Current, Western Australia: longshore steric height gradients, wind stresses and geostrophic flow. J Phys Oceanogr. 1985;15:481–95.View ArticleGoogle Scholar
- Smith RL, Huyer A, Godfrey JS, Church JA. The Leeuwin current off Western Australia, 1986–1987. J Phys Oceanogr. 1991;21:323–45.View ArticleGoogle Scholar
- Smith SD, Banke EG. Variation of the sea surface drag coefficient with wind speed. Q J R Meteorol Soc. 1975;101:665–73.View ArticleGoogle Scholar
- Warner JC, Geyer WR, Lerczak JA. Numerical modeling of an estuary: a comprehensive skill assessment. J Geophys Res. 2005;110:C05001.Google Scholar
- Emery WJ, Thomson RE. Data analysis methods in physical oceanography: second and revised edition. 2001.Google Scholar
- Gallop S, Verspecht F, Pattiaratchi C. Sea breezes drive currents on the inner continental shelf off southwest Western Australia. Ocean Dyn. 2012;62:569–83.View ArticleGoogle Scholar
- Kendrick GA, Aylward MJ, Hegge BJ, Cambridge ML, Hillman K, Wyllie A, et al. Changes in seagrass coverage in Cockburn Sound, Western Australia between 1967 and 1999. Aquat Bot. 2002;73:75–87.View ArticleGoogle Scholar
- Sinclair EA, Gecan I, Krauss SL, Kendrick GA. Against the odds: complete outcrossing in a monoecious clonal seagrass Posidonia australis (Posidoniaceae). Ann Bot. 2014;113:1185–96.View ArticleGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.