Reproduction of annual eelgrass: Variation among habitats and comparison with perennial eelgrass (Zostera marina L.)

The variation in reproductive potential of annual eelgrass was examined along a continuous gradient on an extensive mudflat bordering on and sloping down from the shore (Eastern River) and in a habitat mosaic in a salt marsh (Petpeswick Inlet) in Nova Scotia. Spathe and flower production as well as plant density were compared among habitats. Of the four habitats investigated in Petpeswick Inlet, the largest numbers of spathes and flowers per spathe were produced by plants in ponds on raised flats of Spartina alterniflora Loisel. The highest number of seeds per unit area was produced by plants in depressions on these flats which drained with each low tide. Seed production of annual eelgrass in drained depressions (4 889 seeds per 625 cm²) was seven times that of perennial shoots in creeks and higher than any records in the literature for perennial eelgrass. On average, seed production of annual eelgrass in this study was higher than values reported for other locations. Along the gradient, both annual and perennial eelgrass showed peaks in reproductive potential, but the annual peaked further up the gradient where there was greater exposure to air at low tide. Transplanting studies indicated that the among-habitat differences in reproductive potential were largely controlled by environmental as opposed to genetic factors. The possible effect of inter- and intraspecific competition on the reproductive potential of annual eelgrass was investigated experimentally in two habitats where co-existing species were abundant. In creeks the presence of perennial eelgrass significantly reduced the reproductive potential of annual eelgrass, but in a drained depression, the removal of Ruppia maritima L. s.l. had no effect. The upper distribution limit of annual eelgrass is likely determined by desiccation while the lower limit is probably determined by a combination of light availability (to some extent affected by perennial eelgrass) and exposure to spring rains which would significantly enhance seed germination.     

Light effects on development of an indeterminate plant

The peanut (Arachis hypogaea L.) plant is indeterminate in growth habit and day-neutral with respect to flower initiation. The Spanish-type cultivar used in this study begins flowering 3 to 4 weeks from planting under optimum environmental conditions. In this study, irradiance and photoperiod were used to alter the development of the peanut plant. Plants grown at low irradiance (300 microeinsteins per square meter per second) had the same number of leaves as the plants grown at high irradiance (500 microeinsteins per square meter per second), but they had a larger leaf surface area and were taller than plants grown at the high irradiance. However, flowering and other reproductive components (pegs, pods, and seeds) were reduced at low irradiance. Comparison of 8-, 12-, and 16-hour photoperiods at the high irradiance showed that the 16-hour photoperiod produced the largest amount of vegetative, but least amount of reproductive components. The plants grown at 8-hour photoperiod had one-third as much total leaflet area as plants grown at 16 hours, but six times more weight of mature seeds. The larger amount of photosynthetic surface (leaf area) did not result in more reproductive growth. The results indicate that the peanut plant may readily redistribute its available assimilates between vegetative and reproductive growth in response to irradiance and photoperiod.     

Vertical distribution and seasonal variation of eelgrass beds in Iwachi Bay,Izu Peninsula,Japan

The vertical distribution and population structure of eelgrass beds were surveyed in Iwachi Bay, along the Pacific coast of central Japan. Samplings were conducted from May through November 1977 by SCUBA. Eelgrass was distributed between 3 and 11 m in depth. The relative light intensity at 12 m depth was 11% at the lower range. The highest population density was 290 shoots/m² in September and the fresh weight of biomass was 888 g/m² in July at 7 m depth. The maximum mean leaf area index was about 3 at 10 m depth in July. The ratio of reproductive shoots to the total shoots was about 36% at 7 m depth in June. Eelgrass showed good growth at 7–10 m depth, which is comparatively deeper than other eelgrass habitations. The high values of water transparency and sunshine duration, as well as solar radiation compared with other localities was believed to contribute to the growth of eelgrass in deeper waters in Iwachi Bay.     

Sources of uncertainty in estimation of eelgrass depth limits

In coastal areas seagrasses have considerable ecological importance and respond to eutrophication pressures. Seagrasses have, therefore, become an important parameter for assessing ecological status of marine water bodies. In this study we analyzed the sources of uncertainty associated with the monitoring of the maximum depth limit of eelgrass (Zostera marina). Based on a long-term marine monitoring of eelgrass depth limit in Danish coastal waters we estimated the uncertainty contribution of years, divers, transects, and replicates in water bodies and their sub-areas. For all these components the absolute uncertainty increased with the maximum depth limit. We used either a Spheric or a Gaussian function to describe the relationship between uncertainty and the maximum depth limit for each variable. This parameterization of the depth-specific uncertainty allowed estimation of the total variance associated with monitoring, which can be used to evaluate monitoring designs. The variance components were included in a time budget for optimizing eelgrass monitoring. With a maximum time limit of 100 or 200 h allocated for monitoring, the design that resulted in the lowest variance of the estimated maximum depth limit used 2 or 3 divers, respectively, and involved 2 or 3 years of monitoring and 4–8 transects.     

Photoadaptation and growth of Zostera marina L. (eelgrass) transplants along a depth gradient

Photosynthetic and growth responses were assessed in Zostera marina L. transplants within and beyond the natural extent of an eelgrass meadow in Great Harbor, Woods Hole, MA. Transplant survival and rapid growth inshore of the shallow edge of the meadow (0.5 and 0.8 m water depth) indicated a periodic disturbance factor maintaining the shallow edge of the meadow. Transplant mortality, reduced growth, and a negative carbon balance of eelgrass transplanted offshore the deep edge of the meadow (7 and 10m) supported the hypothesis of light-limited eelgrass growth in the deep regions of the Great Harbor meadow. Photoadaptive responses occurred along the water depth gradient, and both photosynthesis and growth responses were used to assess the genetic vs. phenotypic components of eelgrass response to the water depth gradient. Reciprocal transplants between shallow (1.3 m) and deep (5.5 m) areas within the eelgrass meadow indicated photosynthetic and growth responses were primarily a result of growth habitat rather than genetic differentiation within the eelgrass meadow.     

Effects of light on seagrass photosynthesis,growth and depth distribution

The relationships between light regime, photosynthesis, growth and depth distribution of a temperate seagrass, Zostera marina L. (eelgrass), were investigated in a subtidal eelgrass meadow near Woods Hole, MA. The seasonal light patterns in which the quantum irradiance exceeded the light compensation point (H_comp) and light saturation point (H_sat) for eelgrass photosynthesis were determined. Along with photosynthesis and respiration rates, these patterns were used to predict carbon balances monthly throughout the year. Gross photosynthesis peaked in late-summer, but net photosynthesis peaked in spring (May), due to high respiration rates at summer temperatures. Predictions of net photosynthesis correlated with in situ growth rates at the study site and with reports from other locations.The maximum depth limit for eelgrass was related to the depth distribution of H_comp, and a minimum annual average H_comp (12.3 h) for survival was determined. Maximum depth limits for eelgrass were predicted for various light extinction coefficients and a relationship between Secchi disc depth and the maximum depth limit for survival was established. The Secchi disc depth averaged over the year approximates the light compensation depth for eelgrass. This relationship may be applicable to other sites and other seagrass species.     

Evidence of Eelgrass (Zostera marina) Seed Dispersal by Northern Diamondback Terrapin (Malaclemys terrapin terrapin) in Lower Chesapeake Bay

The initial discovery in May 2009 of eelgrass (Zostera marina) seeds in fecal samples of wild-caught northern diamondback terrapins (Malaclemys terrapin terrapin) was the first field evidence of eelgrass seed ingestion in this species. This finding suggested the potential of terrapins as seed dispersers in eelgrass beds, which we sampled for two additional years (2010 and 2011). Seeds were only found in feces of terrapins captured prior to June 8 in all three years, coinciding with eelgrass seed maturation and release. Numbers of seeds in terrapin feces varied annually and decreased greatly in 2011 after an eelgrass die off in late 2010. The condition of seeds in terrapin feces was viable-mature, germinated, damaged, or immature. Of terrapins captured during time of seed release, 97% were males and juvenile females, both of which had head widths <30 mm. The fraction of individuals with ingested seeds was 33% for males, 35% for small females, and only 6% for large (mature) females. Probability of seed ingestion decreased exponentially with increasing terrapin head width; only males and small females (head width <30 mm) were likely to be vectors of seed dispersal. The characteristic that diamondback terrapins have well-defined home ranges allowed us to estimate the number of terrapins potentially dispersing eelgrass seeds annually. In seagrass beds of the Goodwin Islands region (lower York River, Virginia), there were 559 to 799 terrapins, which could disperse between 1,341 and 1,677 eelgrass seeds annually. These would represent a small proportion of total seed production within a single seagrass bed. However, based on probable home range distances, terrapins can easily traverse eelgrass meadow boundaries, thereby dispersing seeds beyond the bed of origin. Given the relatively short dispersion distance of eelgrass seeds, the diamondback terrapin may be a major source of inter-bed seed dispersal and genetic diversity.     

Factors regulating fruit and seed production in the desert annual Lesquerella gordonii

Summary This study examines the pattern of reproduction and factors that limit the maternal reproductive output in the self-incompatible annual, Lesquerella gordonii. Greenhouse experiments showed that fruits do not abscise and they mature if they contain at least one fertilized (outcrossed) ovule. Field studies showed that flowering increased to a peak and then fell off rapidly, while seed production/fruit decreased through the season. Pollen addition did not increase the number of fruit or seeds per fruit, suggesting that fruit and seed production are not pollinator limited. Addition of water increased fruit and seed production by extending the life of the plant, by increasing the number of stalks which flowered, and by increasing the number of seeds per fruit. This indicates that fruit and seed production are resource limited. Fruits are relatively inexpensive as compared to seeds as over 93% of the water in fruits is contained in the seeds. Fifty-three percent of the plants were lost to herbivory as were 64.6% of the fruits on the remaining plants, indicating that herbivory also limited fruit and seed production. It is hypothesized that high fruit set coupled with variable seed set in L. gordonii is an adaptive response to unpredictable, variable resource levels, and high herbivory risk.     

Effect of alternating magnetic field on ontogenesis and morphophysiological characteristics of radish plants of different magnetic orientation

Effect of weak horizontal alternating magnetic field (AMF) with a frequency of 50 Hz and intensity of 400 A/m on seed formation and morphophysiological characteristics was investigated in radish (Raphanus sativus L.) plants of major types of magnetic orientation (TMO): North–South (NS) and West–East (WE). AMF retarded the passage through all the stages of ontogenesis; as compared with control material, the next leaves emerged slower, and the transition to formation of flower-bearing stems, budding, flowering, and production of pods and mature seeds was delayed. In plants of NS TMO exposed to AMP, the number of pods and seeds and the weight of seeds decreased, while these characteristics rose in WE TMO. AMF acted as an environmental factor differentiating plants’ response depending on their type of magnetic orientation. Dissimilar response to the magnetic field is associated with their physiological status.     

Seed dispersal and seed banks in Aloe marlothii (Asphodelaceae)

Aloe marlothii flowers during dry winter months (July–September) and produces large numbers of wind dispersed seeds. Fire disturbance in a population of several thousand A. marlothii plants at Suikerbosrand Nature Reserve, Gauteng, permitted a series of seed dispersal experiments to be conducted. Germination trials indicated that seedling emergence decreased with increased distance from a well defined aloe stand and burn area margin, with seeds dispersed up to 25 m. Flowering frequency and total seed production were positively correlated with plant height, with seed production estimated to range from 26,000 to 375,000 seeds/plant. Although a large number of seeds are produced by flowering plants the survival rate of seeds did not extend beyond the following flowering season.     

The seagrass, Zostera Marina L.: Plant morphology and bed structure in relation to sediment ammonium in izembek lagoon,Alaska

The relationship between the morphology of eelgrass, Zostera marina L., and ammonium in the sediment interstitial water was examined. The size of eelgrass plants collected from an intertidal terrace showed a consistent relationship with the size of the interstitial ammonium pool. Leaf area, length, and width all showed a linear increase in size towards stations having higher ammonium, while within the stations with the highest ammonium the leaf size was relatively unchanged. The size and extent of the root system in eelgrass varied across the environmental gradient. Eelgrass shoot density and flower abundance were inversely correlated with sediment nitrogen across the eelgrass meadow. Shoot density described a strong logarithmic relation with interstitial ammonium, opposite to the relationships for leaf size. Comparison of these results indicates the importance of sediment nitrogen in determining eelgrass bed structure.     

Variation in reproductive modes and population genetic structures of a monocarpic perennial herb,Cardiocrinum cordatum,in relation to habitat fragmentation

Reproductive systems are recognized as having a profound influence on the extent and structure of genetic variation in plant populations. To investigate the spatiotemporal variation in the reproductive modes (sexual and vegetative reproduction) and population genetic structures of a monocarpic perennial herb, Cardiocrinum cordatum (liliaceae), we selected a variety of habitats (e.g. large forested area including primeval forest, small fragmented secondary forest, and so on) around Sapporo City, Japan. We conducted breeding experiments, monitored the fate and growth of marked individuals for 3 years, and also analyzed the spatiotemporal genetic variation of flowering plants within the populations using allozyme variation. Plants emasculated prior to anthesis produced mature fruits in all populations examined. However, seed production was significantly lower in the small fragmented populations, possibly because of the low availability of pollinators and subsequent pollen limitation. In these fragmented populations, the mature flowering plants tended to be more dependent on vegetative reproduction for their recruitment, because they can only produce flowers once in their lifetime. Genetic diversity using samples from mature flowering plants in each population was lower in the small fragmented populations than in the large populations. In addition, although genotypic compositions in the fragmented populations were more or less similar during the 3 years of the study, the dominant genotypes changed temporally and spatially every year in the large populations. The present study demonstrated that the reproductive features of C. cordatum can be altered in various environmental conditions, such as habitat fragmentation, and these changes considerably affected the population genetic structures and vice versa.     

Clonal Structure,Seed Set,and Self-Pollination Rate in Mass-Flowering Bamboo Species during Off-Year Flowering Events

Bamboos are typical examples of highly synchronized semelparous species. Their mass-flowering events occur at supra-annual intervals but they sometimes flower on a small scale in off-years. If some bamboo ramets (culms) of a genet flower and die in off-years, whereas other culms of the same genet do not flower synchronously, the genet can still survive blooming in an off-year and could participate in the next mass-flowering event. At genet level, the effect might be similar to that achieved by synchronously reproducing iteroparous plants. In addition, if multiple genets flower simultaneously in off-years, cross-pollination will be promoted. However, it is not known whether all the culms in a genet flower synchronously and whether multiple genets flower in off-years. We determined the clonal structure of three temperate dwarf bamboo species, i.e., Sasa senanensis, S. kurilensis, and S. palmata, at 24 off-year flowering sites and the surrounding areas in northern Japan using seven microsatellite markers. We also estimated seed set at seven of the sites and self-pollination rates at five sites to determine off-year reproductive success. Next, we investigated whether seed sets at the culm level were related to flowering area and/or number of flowering genets, using generalized linear mixed-effect models (GLMMs). Multiple genets flowered at 9/24 flowering sites. We found that 40/96 of the genets identified had some flowering culms. Non-flowering culms were present in 24/40 flowering genets. Seed set was in the range 2.2%–12.5% and the self-pollination rate was 96.3%. In the best GLMM, seed set increased with flowering area. Seeds were produced in off-years, but cross-pollination was rare in off-years. We suggest that some dwarf bamboos may exhibit iteroparity or imperfectly synchronized semelparity at the genet level, a characteristic similar to that of other reproductively synchronous plants. We also found synchronous flowering of a few genets even in off-years.     

The effect of pollination on the growth and reproduction of oilseed rape (Brassica napus)

Phenotypic plasticity is an organism's ability to alter its development and life history in response to environmental conditions. In plants, biotic and abiotic factors drive the distribution of resources between growth and reproductive traits. One such biotic factor is pollination. Studies show that wind and insect pollination enhance oilseed rape (Brassica napus) yield. However, the impact of pollination on resource allocation towards growth and reproduction is less understood. We conducted a controlled experiment to assess the effect of pollination on growth and functional reproductive traits. We compared two simulated supplementary pollen deposition methods (representing wind and insect pollination) alongside a non-supplementary control. Pollinated plants allocated resources towards growth and reproduction similarly, irrespective of deposition method. Plants receiving no supplementary pollination produced fewer seeds, allocating resources to growth, more prolific and persistent flowering, and heavier seeds. Pollinated plants had a reduced flowering period and were shorter, indicating resources were allocated to seed production rather than growth or the production of additional flowers. This allocation of resources from growth and flowering metrics can increase yield directly through increased seed production and indirectly through shorter plants and a reduced flowering period with seeds that mature earlier (agronomically beneficial traits).Wind and insect pollination can enhance and stabilise oilseed rape yield under various environmental conditions by acting in complementary ways. Since pollination limits yield in oilseed rape, it must be considered an input that can be actively managed. Successful management of pollination services requires growers to detect pollination deficits. Inadequately pollinated oilseed rape plants exhibit apparent morphological changes (e.g. taller plants that flower for longer), acting as an early warning to growers. Equipping growers with this knowledge provides them with a means of detecting deficits and thus enables them to take positive action to restore pollination services by introducing honeybees or enhancing wild pollinators.     

Altitudinal variation in flowering area and position and their ecological significances of an alpine cushion Arenaria polytrichoides,a gynodioecious herb

Aims As foundation species in the alpine ecosystems, the reproduction and recruitment of alpine cushion plants are very important for sustaining the alpine ecosystem functions. However, it still remains unclear that how cushion plants effectively allocate resources to optimize reproductive fitness.Methods Here we selected five populations of a gynodioecious herb Arenaria polytrichoides with different exposures and slopes along an altitudinal gradient on the Baima snow mountain in northwest Yunnan, southwest China, to investigate and compare flowering area and positions, within and among populations and between female and hermaphroditic morphs. By doing so, we further discuss how the environmental stresses affect the cushion’s flowering attributes thus the population-level reproduction.Important findings The results showed that, individual plant size and resources allocated to flowering (flowering area %) both decreased with increasing elevation, indicating that the reproductive allocation strategy was significantly affected by elevation. However, a population at lower elevation showed lower reproductive investment than higher populations, suggesting that elevation was not the only factor affecting the cushion’s reproductive allocation. In addition, absolute flowering area increased with increasing individual size, but the flowering area ratio decreased, indicating that the increases in reproductive allocation are fewer than that in vegetative allocation. Hermaphroditic individuals invested more resources to flowering than females did, but again, such effect was affected by elevation. Moreover, within a single population, the flowering areas were significantly different among the four directions (east, south, west and north) within one single individual canopy, but such differences varied in different populations.     

高山垫状植物团状福禄草开花面积与方位随海拔的变化及其适应性

作为高山生态系统中的奠基种(foundation species), 垫状植物自身种群的繁殖与扩张, 对高山生态系统功能稳定性起着关键作用。但是, 垫状植物如何在极端环境条件下实现资源的有效利用与分配, 达到繁殖最优化, 至今鲜为人知。该研究在滇西北白马雪山沿海拔梯度选择具有不同坡度及坡向的5个团状福禄草(Arenaria polytrichoides)种群, 调查、比较种群内、种群间以及具有不同性系统的植株个体之间的开花面积比、开花方位, 并分析不同生态因子对其开花特性的影响。结果表明: 随着海拔的升高, 团状福禄草个体变小, 其分配到开花的资源比例总体上随海拔上升呈现下降的趋势, 说明团状福禄草的繁殖分配受到由海拔所引起的生态因子的调控。但是, 部分低海拔种群内植物个体的繁殖分配显著低于部分高海拔种群, 说明海拔并非控制植物繁殖分配的唯一因素。此外, 植株开花总面积随植株个体增大而增加, 但开花面积比却随个体增大而变小, 说明植株分配到开花的资源增长速率可能低于植株个体的增长速率。在性别差异方面, 两性植株对开花的资源分配比例要显著高于雌性植株, 但是, 其差异程度受到海拔因素的影响。最后, 在同一种群内, 团状福禄草在冠层表面不同方位上的开花面积比存在显著差异性, 这种差异性在不同种群之间又具有不同的表现形式。     

Effects of resource availability, and fruit and ovule position on components of fecundity in Alliaria petiolata (Brassicaceae)

In four field and glasshouse experiments designed to alter the supply of resources through manipulation of nutrients, root tissue, leaf area and fruit number in Alliaria petiolata (Brassicaceae), more than 99% of ovules per plant showed signs of fertilization, suggesting that seed production in this plant was not pollen limited. However, in all treatments a significant proportion of fruits and seeds did not develop to maturity. Total fruit and seed production did not differ significantly from controls when plants were given nutrient supplements at flowering. Removal of 50–75% of the root tissue in 1-yr-old plants significantly reduced fruit set, but had no effect on individual seed development. Removal of cauline leaves significantly reduced most measures of fruit and seed production, suggesting that current photosynthate is critical for fruit and seed filling. Seed maturation was significantly affected by both fruit position within an infructescence and ovule position within a fruit. Basally located fruits and ovules (within fruits) developed more mature seeds than distally positioned fruits and ovules. Plants responded to removal of basal fruits by re-allocating resources to distal fruits that would normally have aborted. Our results suggest that fruits and seeds act as reproductive sinks competing for parental photosynthate. Patterns of resource allocation within infructescences and fruits were also modified by our experiments.     

A simulation model of production,seasonal changes in biomass and distribution of eelgrass (Zostera marina) in Lake Grevelingen

Summary A simulation model has been described, based on data from Lake Grevelingen, The Netherlands, as a predictive tool for lake management. The model has been developed as part of a large-scale aquatic modelling effort in Lake Grevelingen, carried out in close cooperation with the Delft Hydraulics Laboratory and the Delta Department, Environmental Research Division of the Ministry of Transport and Public Works. Available data on growth rates per unit eelgrass biomass, obtained with the leaf-marking technique, and on above- en below ground biomass and shoot density changes per unit area have been used. A space limitation depending on density of the above ground biomass and a growth limitation due to shortage in below ground biomass have been introduced. The seasonal changes in eelgrass production, both above and below ground, have been simulated as functions of the external forcing variables light, water temperature, wind generated water movements and of the internal control variables due to aging of the plant material. The vertical distribution of eelgrass can be partly explained from the modelling results on space, light and below ground biomass limitations. From the shore down to about 1 m waterdepth the above ground eelgrass biomass suffers from space limitation. Between 1 and 2 m production and biomass reach maximum values. Between 2 and 3 m waterdepth the above ground eelgrass growth is limited by the availability of below ground biomass. Between 3 and 5 m waterdepth both below ground biomass and light are the growth-limiting factors. Below 5 m waterdepth light is not sufficient to sustain net growth of eelgrass from rhizomes. Together with additional data — not used in the model — on seed production and growth of eelgrass shoots from seeds the vertical and horizontal distribution of the dominant macrophyte in the lake can be explained.     

Population ecology on an environmental gradient: Cakile edentula on a sand dune

Summary A naturally-occurring sand dune population of the annual plant Cakile edentula (Brassicaceae) was studied for two years. The plants grew along an environmental gradient stretching from open sand beach (seaward) to densely vegetated dunes (landward). Survivorship and reproductive output were estimated from plants in permanent quadrats. The dispersal of seeds was documented by sifting fruits from the sand substrate at different seasons.Seedlings germinate in April and May and begin flowering in July and August. They may continue to flower until October unless destroyed by autumn winds or heavy frost. Although seaward plants germinate approximately a month later than landward plants, they grow more rapidly and by September may be two orders of magnitude larger than landward plants (dry weight of vegetative parts 6.86±3.97 g compared to 0.029±0.006 g; dry weight of fruits 5.92±4.27 g compared to 0.016±0.005 g; mean with 95% CI). In both years, seedling survivorship and mature plant reproductive output declined significantly with distance landward. The large plants at the seaward end of the gradient produced most of the fruits (144 and 278 fruits per capita in 1975 and 1976 respectively) but a large proportion of these were moved landward by wind and waves during the winter. Thus, at the seaward end of the gradient, the main influx on individuals was from reproduction, and the main loss of individuals was from dispersal landward during the winter. The small plants at the landward end of the gradient produced few fruits (1.8 and 1.2 fruits per capita in 1975 and 1976 respectively), and mortality greatly exceeded this reproductive output. Thus, at the landward end of the gradient, the main loss of individuals was through seedling mortality, but this was balanced by a large annual influx of individuals from the seaward end of the gradient. Plants at the landward end of the gradient therefore exist only because of annual dispersal of seeds landward. Most seeds produced at the seaward end of the gradient disperse from an area of good habitat (high survivorship and high reproductive output) to an area of poor habitat (low survivorship and low reproductive output).     

DISPERSION OF SEEDLINGS OF THE PRAIRIE COMPASS PLANT,SILPHIUM LACINIATUM (ASTERACEAE)

Although the dispersal of seeds around individual plants (the seed shadow) has frequently been characterized, the dispersion of seedlings around plants (the seedling shadow) has rarely been examined. We mapped 101 and 149 seedlings of the prairie compass plant (Silphium laciniatum) that appeared in our study area in 1987 and 1990 following mass flowering in 1986 and 1989. We also mapped the locations of flowering stems which appeared in 1986 and 1989 and recorded the number of flowerheads at each stem location. The frequency distributions of distance between a seedling and the nearest flowering stem were identical in the 2 years, with a median distance of 1.0 m. The large size and lack of wind-dispersal structures of compass plant seeds (achenes) are responsible for their limited dispersal. From estimates of the total seed production in the study area in 1986 and 1989, we calculated that about 1% of seeds became seedlings in each year. Flowering stem locations with a higher number of flowerheads had a significantly higher density of seedlings around them. This indicates that recruitment to compass plant populations is not a “lottery”; individual plants that produce more seeds produce, on average, more seedlings.