Regeneration of monsoon rain forest in northern Australia: the dormant seed bank

Abstract. As part of a wider study examining regeneration pathways in monsoon rain forest vegetation in northern Australia, the dormant component of the soil seed bank was assessed by storing soil samples for over six dry season months, before watering in shade-house trials. Six soil samples were collected from each of 34 sites broadly representative of the range of regional monsoon rain forest vegetation. Four floristic seed bank groups were derived through TWINSPAN classification. Mean group densities of germinants ranged from 25–144/m². Dormant seed banks were least dense, and most sparsely distributed, in sandy soils. Seed bank samples were dominated by woody pioneer monsoon rain forest species, especially figs; exotic weeds and savanna taxa (e.g. Poaceae) were relatively more common at seasonally dry sites. Dormant seed banks comprised species mostly present in the standing vegetation, although a small number of germinants represented species not growing at half the sites. Regeneration of woody pioneers from dormant seed banks is least likely to be of importance on infertile, seasonally dry sites.     

The impact of flooding regime on the soil seed bank of flood‐meadows

Abstract. We assessed the significance of flooding for the floristic composition of seed banks in flood‐meadows of the northern valley of the Upper Rhine. We compared three hydrological compartments of the alluvial plain, consisting of the regularly flooded land between the river and low summer dykes (functional flood‐plain), the occasionally flooded land between summer dykes and high winter dykes (hybrid floodplain) and the land behind the winter dykes, which is now only submerged by ascending groundwater (fossil flood‐plain). Due to their different flooding regime, the three compartments should differ with respect to the prevailing conditions of diaspore input. The seed density of soil samples increased with the duration of flooding in the three compartments, while species richness and the proportion of species not occurring in the vegetation was constant. The increase in seed density can be largely attributed to an increase of disturbance indicators, which are present in the above‐ground vegetation and capable of forming a long‐term persistent seed bank. No effects of flooding on the composition of seed banks in the three flood‐plain compartments were found. The differences in seed bank composition can be largely explained by corresponding differences in above‐ground vegetation and former and present‐day meadow management. Seeds of species absent from above‐ground vegetation can be attributed to the local species pool present in the immediate vicinity of the study plots. We discuss consequences of the results for the restoration of species‐rich flood‐plain meadows.     

Fire,aridity and seed banks. What does seed bank composition reveal about community processes in fire‐prone desert?

Questions: The relationship between fire, aridity and seed banks is poorly understood in plant community ecology. We tested whether there was a close correspondence between the seed bank and standing vegetation composition with time‐since‐fire in a desert. We also examined whether longer‐lived species showed seed limitation relative to more ephemeral species, as this could influence grass‐woody ratios in a major biome. Location: Dune hummock grasslands/shrublands of central Australia. Methods: The effects of time‐since‐fire on floristic and functional group composition were examined by comparing plots unburned since 1984 against plots that had been burned in 2002. Three methods were used to quantify seed abundances: a germination trial using heat and smoke application, a flotation method, and a sieving method. Results: Seed bank densities were very low (<3000 m^?2). Species similarity between the seed bank and standing vegetation was high at sites recently burned (0.86) and low in sites long‐since burned (0.52). The relative abundance of ephemeral species in the seed bank peaked in recently burned plots, but the relative abundance of seeds of woody species did not match the pattern of abundance in the standing vegetation. Remarkably, the dominant perennial grasses and woody species were either absent from the seed bank or present at extremely low abundances. Discussion: Differences in the relative abundance of ephemeral species between standing vegetation and seed bank relate to the post‐fire succession process. The small soil pool of seed from woody species may be explained by allocation to belowground carbohydrate storage over seed production. Field observations suggest, however, that production of strongly dormant seed can be prolific and that high levels of seed predation make this system strongly seed‐limited. The discovery of this seed bank syndrome indicates that shifts in grass‐woody ratios can be driven by the juxtaposition of unpredictable seed rain and fire events in these desert dunes. However, estimates of grass‐woody ratios due to changing fire regimes will be difficult to predict.     

The role of the seed bank,seed rain and the timing of disturbance in gap regeneration

Abstract. Question: Does the degree and timing of disturbance contribute significantly to the pattern and process of regeneration in plant communities as a consequence of the availability and number of species of propagules present? Location: Acid grassland at 230 m a.s.l., eastern Scotland, UK. Methods : Plots were surface disturbed or had their soil profile inverted at monthly intervals at 12 dates during a year. Seed bank and seed rain were assessed at each treatment time. The effect of disturbance intensity and timing on the regenerating vegetation was assessed. Results: Removing the seed bank significantly slowed regeneration, as it contributed 43 % of developing cover after one year where it was present. At an individual seed level, seed in the seed rain had a much higher likelihood of contributing to the regenerating vegetation than a seed in the seed bank. Some species showed a reliance on the seed bank for regeneration, and hence there was a significant difference in the vegetation that developed between plots with the seed bank intact and those where it was removed. Winter disturbed plots (little seed rain) had slower rates of re‐vegetation than summer disturbed plots. Timing had little effect on species composition, though a significantly higher cover of perennial forb species developed on the winter disturbed plots. Conclusion: Removing the contribution of the seed bank had a greater effect on the composition of regenerating vegetation than the effect of seasonal variation on the seed rain.     

Resilience,persistence and relationship to standing vegetation in soil seed banks of semi‐arid Australian old fields

Questions: Do soil seed banks of semi‐arid grasslands reassemble after abandonment from cultivation? Do seeds of native and exotic species persist in the soil? Does time since abandonment affect compositional similarity between the vegetation and seed bank? Does the seed bank contribute to resilience in the vegetation? Location: Native grasslands in northern Victoria, Australia. Methods: Seed bank sampling was conducted in spring and autumn over 3 yrs, across a 100‐yr chronosequence. Species richness, composition and germinant density were determined using the seedling emergence method. Seed persistence was assessed by comparing seed densities in spring and autumn. Seed bank composition was compared with the vegetation. Results: The spring seed bank was dominated at all stages by sedges and rushes; hence, native species richness and seed density were largely unaffected by abandonment. In autumn, grassland species contributed more to the seed bank, but richness was reduced after abandonment and showed little recovery, although seed density partially recovered. Seed bank composition showed some recovery in both seasons. Most species had low persistence in the soil. Compositional similarity between the vegetation and seed bank was greater in old fields than uncultivated grasslands in spring, but not autumn. Conclusions: Resilience varied among seed bank parameters and seed banks had low functional importance. Patterns in the seed bank followed, rather than caused, those in the vegetation. Thus, vegetation recovery cannot rely on the seed bank and persistent seeds were not the key mechanism of resilience in the vegetation.     

Regeneration by seeds in alpine meadow and heath vegetation in sub‐arctic Finland

Abstract. This paper compares the regeneration by seeds of heath and meadow and studies relationships between the floristic composition of phases in the regeneration pathway. Seed densities in the seed rain and seed bank as well as the densities of emerged seedlings in gaps and in closed vegetation were greater in the meadow than in the heath. In the heath, environmental constraints hindered seedling emergence almost completely so seeds accumulated in the seed bank. In the meadow, the decrease in the seed bank was due to high seedling emergence. Within both plant communities, seedling emergence in gaps and in closed vegetation was comparable. In the meadow, the seed rain and seedling emergence in gaps, as well as the seed bank and seedling emergence in gaps were positively correlated. Differences in seed and adult plant sizes were reasons for the low correlation between the standing vegetation and the other phases. In DCA ordination the first axis separated the phase of seedling emergence in closed vegetation and seed bank. The second axis separated the standing vegetation from the other phases. The structure of the seed rain was more heterogeneous than that of other phases. In the heath, the standing vegetation and the seed rain were positively correlated. The ordination of these phases reflected the patchiness of standing vegetation and the ability of the diaspores of Betula nana to disperse over long distances.     

Long‐term seed bank dynamics in a temperate forest under conversion from coppice‐with‐standards to high forest management

Questions: How do changes in forest management, i.e. in disturbance type and frequency, influence species diversity, abundance and composition of the seed bank? How does the relationship between seed bank and vegetation change? What are the implications for seed bank dynamics? Location: An ancient Quercus petraea — Carpinus betulus forest in conversion from coppice‐with‐standards to regular Quercus high forest near Montargis, France. Methods: Seed bank and vegetation were sampled in six replicated stand types, forming a chronosequence along the conversion pathway. The stand types represented mid‐successional stages of stands in transition from coppice‐with‐standards (to high forest (16 plots) and early‐ and mid‐successional high forest stands (32 plots). Results: Seed bank density and species richness decreased with time since last disturbance. Adjusting for seed density effects obscured species richness differences between stand types, but species of later seres were nested subsets of earlier seres, implying concomitant shifts in species richness and composition with time since disturbance. Later seres were characterized by species with low seed weight and high seed longevity. Seed banks of early seres were more similar to vegetation than to later seres. Conclusions: Abandonment of the coppice‐with‐standards regime altered the seed bank characteristics, as well as its relationship with vegetation. Longer management cycles under high forest yield impoverished seed banks. For their persistence, seed bank species will increasingly rely on management of permanently open areas in the forest landscape. Thus, revegetation at the beginning of new high‐forest cycles may increasingly depend on inflow from seed sources.     

Hidden biodiversity in the Arctic – a study of soil seed banks at Disko Island,Qeqertarsuaq, West Greenland

Seed dispersal is a key process in plant community dynamics, and soil seed banks represent seed dispersal in time rather than in space. Despite their potential importance, seed bank dynamics in the Arctic are poorly understood. We investigated soil seed banks and corresponding plant community composition in three contrasting vegetation types in West Greenland, viz. dwarf shrub heaths, herb slopes and fell‐fields. Through germination testing, 31 species were documented in soil seed banks. All of these were herbaceous, while no dwarf‐shrub species, which represents the dominating growth form in the above‐ground vegetation, were emerging from the seed bank. Consequently, across vegetation types, the lowest similarity between seed bank and above‐ground vegetation was found in dwarf shrub heath. Nine plant species were exclusively found in seed bank, all of which were non‐clonal forbs. Seed bank size (total number of seeds) and species richness seemed to increase with the level of natural disturbance. Additionally, we examined the effect of different experimental light and temperature conditions on the quantity and diversity of germinating seeds. The difference in diversity in vegetation and seed bank at the species level will impact population dynamics, regeneration of vegetation after disturbances and its potential to respond to climate change.     

Restoration of the Cirsio dissecti‐Molinietum in The Netherlands: Can we rely on soil seed banks?

Abstract. Vegetation and soil seed banks of a threatened Atlantic fen meadow community were studied using recent phytosociological records and seedling emergence from soil samples. Similarly managed but differently degraded stands that suffered different levels of species impoverishment were compared. The actual vegetation was related to a set of phytosociological references representing the subassociations of the community. DCA positions of reference relevés from the different subassociations were overlapping, suggesting that in all references many common species occur. Recent records were positioned in‐between the seed bank samples and the references. The soil seed banks of all stands were dominated by ordinary species. Most character species had at most sparse seed banks and no seedlings of locally extinct character species, mentioned in historic floristic records, were detected. In contrast species of pioneer and small‐sedge communities as well as those of heathlands were abundant in the seed banks. Based on the vertical distribution of seeds in the soil layers most fen meadow species were classified into transient or short‐term persistent seed bank types. We concluded that complete restoration of the Cirsio dissecti‐Molinietum without reintroduc‐tion is only likely in stands that were degraded only a few years ago. On the other hand, the presence of viable seeds of Nanocyperion and Parvocaricetea species is promising for the restoration of these communities even after decades. Recreation of pioneer habitats by sod cutting will preserve these species.     

土壤种子库的研究进展及若干研究热点

 土壤种子库是指存在于表层土壤（包括凋落物）中的有生命的种子。土壤种子库的研究已是植物生态学研究不可缺少的一部分,现已成为植物种群生态学中比较活跃的领域。土壤种子库时期是植物种群生活史的一个重要阶段,有人称之为潜种群阶段。土壤种子库对一年生植物来说尤其重要。土壤种子库简单地可分为瞬时土壤种子库和长久土壤种子库,即使给予理想的萌发条件如季节、温度、湿度等,土壤种子库中也仍有部分种子保持休眠状态,休眠的种子组成了土壤长久种子库的成分。时空异质性是土壤种子库的基本特性之一,不仅不同植被类型的土壤种子库具有不同的组成、大小和多样性,而且微环境也影响土壤种子库的分布格局。由于萌发、捕食和衰老等原因,土壤种子库具有季节动态,一般在旧种子萌发之后,新种子散布之前达到最低点。在高等植物占据的大多数生境中,以休眠繁殖体形式存在的个体远远超过地上植株的数量;土壤种子库、幼苗库和成年植被相互联系相互影响。由于各种原因如群落类型的差异、群落的演替阶段、取样的时间等,地上植被和土壤种子库之间关系大体上可分为两种情况,即相似性和差异性;研究土壤种子库的方法通常有萌发法和物理分离法。土壤种子库能部分反应群落的历史,对退化生态系统的恢复起着重要的作用。目前土壤种子库的主要研究热点问题可分为以下几个方面：1）土壤种子库的研究方法,2）土壤种子库的分类问题,3）土壤种子库分布的时空格局,4）地上植被和土壤种子库的关系,5）土壤种子库的动态等。     

Relationships among the seed rain,seed bank and vegetation of a Hawaiian forest

Abstract. Hawaiian ecosystems are prone to invasion by alien plant species. I compared the seed rain, seed bank, and vegetation of a native Hawaiian forest to examine the potential role that seed ecology plays in allowing alien species to invade native forest. Absolute cover of seed plants in the forest was 126 %, annual seed rain was 5 713 seeds m^-2 yr^-1, and the mean density of seedlings emerging from the seed bank averaged across four seasons was 1 020/m². The endemic tree Metrosideros polymorpha was the most abundant species in the vegetation, seed rain and winter seed bank. Overall, native seed plants comprised 95 % of the relative cover in the vegetation and 99 % of the seeds in the seed rain, but alien species comprised 67 % of the seeds in the seed bank. Alien species tended to form persistent seed banks while native species formed transient or pseudo-persistent seed banks. Dominance of the seed bank by alien species with persistent seed banks suggests that aliens are favorably placed to increase in abundance in the vegetation if the forest is disturbed.     

Soil seed bank dynamics in alpine wetland succession on the Tibetan Plateau

The primary goal was to address several questions with regard to how soil seed banks change in a successional series. How does the composition of the viable seed bank change, and how does the relationship of the soil seed bank and vegetation change with succession? Can the seed bank be regarded as a potential as a source of seeds for wetland restoration? We collected soil seed bank samples and sampled the vegetation in four different successional stages and used the NMDS (nonmetric multidimensional scaling) to evaluate the relationship of species composition between the seed banks and vegetation. The difference of seed density and species richness in different habitats and soil depths also was compared. Viable seeds of half (37) the species in the early-successional stage were found in all the successional stages. Similarity between seed bank and vegetation increased with succession. Both seed density and species richness in the seed bank increased with successional age and decreased with soil depth. The majority of species from the early-successional stage produced long-lived seeds. Seed density and species richness increased with succession, mainly as a result of increasing seed production, and hypotheses predicting decreasing density of buried seeds and species richness were not confirmed. Seed banks play a minor role in contributing to the regeneration of vegetation, and managers cannot rely on soil-stored seed banks for restoration of wetlands.     

Similarity between seed bank and vegetation in Mediterranean grassland: a predictive model

Abstract. The similarity in species composition between seed bank and vegetation was analysed in Mediterranean grasslands in relation to altitude, topography and grazing. Soil samples were collected in permanent plots in autumn at the end of the summer drought period and in spring, before the new seed fall and after the natural winter seed stratification. The seed bank composition was determined by greenhouse germination over a nine-month period. Presence/absence of species in the standing vegetation throughout the complete annual cycle, and the percentage area of bare ground in October, were recorded in the same plots. The species composition of the standing vegetation is clearly determined by altitude, topography and grazing, while the floristic composition of the seed banks is only related to altitude and topography in the case of autumn seed bank and with any of the three factors in the spring seed bank. Relative abundances of grasses, legumes and forbs also show different patterns in vegetation and seed bank data. Sørensen similarity between the autumn seed bank and the vegetation declines as altitude rises, but there are no significant differences for topography and grazing. This similarity decreases in the case of the spring seed bank and does not show any significant relationship with any of the factors. The perennial/ annual ratio and the proportion of bare soil in October are proposed as explanatory variables in a predictive model of similarity between the seed composition of the seed bank and vegetation.     

Seed banks of temperate deciduous forests during secondary succession

Question: (i) How does former land use and land use intensity affect seed bank development during post‐agricultural succession? (ii) How does time since the last clear‐cut change seed bank composition during post‐clear‐cut succession? Methods: One data set was compiled per succession type using the following selection criteria: (i) the data set included a successional series, (ii) plots were located in mesotrophic forest plant communities and (iii) vegetation data were available. The post‐agricultural succession data set comprised 76 recent forest plots (eight studies); the post‐clear‐cut succession data set comprised 218 ancient forest plots (three studies). Each data set was analysed separately using either linear mixed models or generalized linear models, controlling for both environmental heterogeneity and variation between study locations. Results: In the post‐agricultural succession data set, land use and time significantly affected nearly all the studied seed bank characteristics. Seed banks on former arable land recovered poorly even after 150 year of restored forest cover, whereas moderate land use intensities (grasslands, heathlands) yielded more rapid seed bank recovery. Time was a significant determinant of all but two soil seed bank characteristics during post‐clear‐cut succession. Seed banks in managed ancient forest differed strongly in their characteristics compared to primary forest seed banks. Conclusions: Forest seed banks bear the marks of former land use and/or forest management and continue to do so for at least 150 years. Nevertheless, time since the last major disturbance, being either former land use or clear‐cutting, remains a significant determinant of the seed bank.     

Depth distribution and composition of seed‐banks in alien‐invaded and uninvaded fynbos vegetation

South African fynbos vegetation is threatened on a large scale by invasive woody plants. A major task facing nature conservation managers is to restore invaded areas. The aim of this study was to determine the restoration potential of fynbos following dense invasion by the Australian tree Acacia saligna. The impacts of dense invasion on seed‐bank composition and depth distribution were investigated to determine which fynbos guilds and species have the most persistent seed‐banks. Soil samples were excavated at three different depths for invaded and uninvaded vegetation at two sand plain and mountain fynbos sites. Seed‐banks were determined using the seedling emergence approach. Invasion caused a significant reduction in seed‐bank density and richness at all sites. There was a significant, but smaller, reduction in seed‐bank density and richness with soil depth at three sites. Seed‐bank composition and guild structure changed following invasion. Low persistence of long‐lived obligate seeders in sand plain fynbos seed‐banks indicates that this vegetation type will be difficult to restore from the seed‐bank alone following alien clearance. The dominance of short‐lived species, especially graminoids, forbs and ephemeral geophytes, suggests that regenerating vegetation will develop into a herbland rather than a shrubland. It is recommended that seed collecting and sowing form part of the restoration plan for densely invaded sand plain sites. As seed density remained higher towards the soil surface following invasion, there is no general advantage in applying a mechanical soil disturbance treatment. However, if the shallow soil seed‐bank becomes depleted, for example following a hot fire through dense alien slash, a soil disturbance treatment should be given to exhume the deeper viable seed‐bank and promote recruitment.     

Vegetation and seed bank in a calcareous grassland restored from a Pinus forest

Question: What is the importance of the seed bank in the maintenance of the restoration potential of a 60‐year‐old abandoned calcareous grassland overgrown by Pinus trees? Location: ‘Les Pairées’, province of Luxembourg, Belgium. Methods: The seed bank and the above‐ground vegetation were surveyed in three adjacent stands, previously forming a unique calcareous grassland: a 60‐year‐old Pinus forest, a four‐year‐old clear‐cutting and a typical calcareous grassland. Floristic diversity was compared among stands and between vegetation and seed bank. Results: The species richness of the vegetation and the seed bank was significantly lower in the Pinus forest. More floristic similarities were found between the clear‐cutting and the calcareous grassland. Seed bank was essentially transient, dominated by annual species. Its correspondence with the above‐ground vegetation was weak. Conclusion: Very few calcareous grassland species have persisted in the Pinus stand. Four years after clear‐cutting, the stand was nearing restoration towards a calcareous grassland. Seed longevity in the soil was not the most explicative factor. Dispersal of propagules from adjacent sources was also important.     

Disturbance regimes as determinants of seed banks in coastal dune vegetation of the southeastern Cape

Soil-stored seed banks of grassland, fynbos and thicket, all growing on calcareous dunes and each subject to different disturbance regimes, were examined. Seed banks were determined from counts of germinants from 50 soil cores from each type. Aboveground estimates of plant species cover in 10 1-m² plots were used in determining vegetation/seed bank similarities. There was no evidence for seed bank densities to be markedly higher in the most frequently disturbed community (grassland -4273 seeds/m²) than the least disturbed community (thicket - 3417 seeds/m²). Highest similarity between seed bank and above-ground vegetation composition in terms of species and growth form/life-span classes was recorded for grassland (CC = 50%). Lowest similarity (CC = 13%) was found in the less frequently disturbed thicket where no seeds of climax trees were recorded in the seed bank. A fynbos community on a north-facing (warm, dry) slope had intermediate-sized seed banks (1683 seeds/m²) with intermediate vegetation/seed bank similarity (CC = 46%). However, on the south-facing slope, which has a large post-fire ephemeral herb component, seed banks were larger (4518 seeds/m²) but less similar to above-ground vegetation (CC = 39%o). Ordination (DCA) of vegetation data from the four communities was different from an ordination of their seed bank data. Fynbos shrub species were absent from seed banks of both grassland and thicket, even though secondary succession proceeds from grassland, through fynbos to thicket. Their seed banks appear less persistent than those of European heath or Californian chaparral shrubs.     

Influence of fire on critically endangered Swartland Shale Renosterveld in the Cape Floristic Region

Questions

The degree to which renosterveld shrublands are fire‐dependent is currently unclear. To address this issue, the following questions were asked: (1) does smoke stimulate germination of soil‐stored seeds in renosterveld; (2) does recently‐burned renosterveld display changed composition and higher diversity than unburned vegetation; and (3) how do the species compositions of renosterveld soil seed banks and standing vegetation compare?

Location

Swartland, Cape Floristic Region, South Africa.

Methods

Soil seed bank samples from a north‐ and south‐facing slope were smoke‐treated and germinated to test for smoke‐stimulated germination. Burned standing vegetation was surveyed 16 months post‐fire, as was unburned vegetation on the same slopes. Seed bank species richness and density were compared between smoke‐treated and untreated samples within and between slopes. Burned and unburned standing vegetation were compared within and between slopes in terms of species richness, abundance and aerial cover. Compositional similarity of the seed banks and standing vegetation was assessed.

Results

Seed banks were dominated by annuals and graminoids. Smoke treatment had no effect, except for driving significantly higher species richness and seedling density in south‐facing slope perennial shrubs. Species richness and seedling density were significantly higher in seed banks on the south‐facing slope compared to the north‐facing slope. Burned standing vegetation exhibited significantly higher diversity than unburned vegetation. Annuals and graminoids displayed significantly higher species richness and aerial cover in burned renosterveld. The north‐facing slope contained less than half the number of species/m² compared to the south‐facing slope. The seed banks and standing vegetation showed low to intermediate similarity (Sørensen = 31%–53%), but grouped close together on an NMDS plot, suggesting intermediate similarity overall.

Conclusions

Elevated germination of perennial shrubs in smoke‐treated seed bank samples and increased diversity of post‐fire standing vegetation suggest the renosterveld in this study shows elements of a fire‐driven system. Certain species only recruited in burned sites, suggesting fire‐stimulated germination. Aspect had a major influence on plant community composition, with the mesic south‐facing slope being more diverse than the xeric north‐facing slope. The similarity between the seed banks and standing vegetation was higher than previously shown for renosterveld, and appears to be higher than for fynbos.     

Harvester ants modify seed rain using nest vegetation and granivory

1. In annual plant communities, the seed bank determines each generation's potential emergence and any factor that influences it could alter community structure. Harvester ants are common seed predators that may cause seed sources and seed rain composition to vary. 2. In semi‐arid shrubland of the Negev desert of Israel, we hypothesised that the positive effects of dense vegetation on nests of the harvester ant Messor ebeninus Sant. would outweigh reduction by granivory. 3. To test whether nests were seed sources, we removed vegetation on 10 of 20 sampled nests prior to seeding. We tested the interaction between seed sources and granivory by locating seed traps at three locations: nests, foraging trails, and unvisited areas. Trapped seeds were recorded during spring and summer dispersal. Plant recruitment from the altered seed bank was recorded the following spring. 4. During April, seeds were more abundant near nests than the other locations and at uncut compared with cut nests. Foraging trails had fewer species and higher equitability compared with nests or unvisited areas. May and June to August had highest species richness at nests, but richness of cut and uncut nests were similar. Ordination of plant recruitment showed slightly lower vegetation community variation by diminished species in the cut seed bank. 5. While intact nest vegetation initially had high abundance of locally deposited seeds, it apparently blocked wind‐dispersed seeds later in the summer. Conversely, granivory reduced seed species richness only on trails and decreased dominance structure by preferential removal of some species.     

Role of soil seed bank along a disturbance gradient in an alpine meadow on the Tibet plateau

We examined the role of the soil seed bank along a grazing disturbance gradient and its relationship with the vegetation of alpine meadows on the Tibet plateau, and discussed the implications for restoration. The seed bank had a high potential for restoration of species-rich vegetation; 62 species were identified in the vegetation and 87 in the seed bank, 39 species being common to both. Mean seed density was 3069–6105 viable seeds m⁻². The density of buried seeds increased significantly with increasing disturbance, indicating that restoration of disturbed areas is not seed limited. Seed density and species richness decreased with depth. The proportion of perennial species decreased with decrease in disturbance both in seed bank and in vegetation. A large portion of species with persistent seeds in the disturbed areas indicate that this seed type can be regarded a strategy of adaptation to current disturbances. Detrended correspondence analysis (DCA) showed significant differences of species composition between seed bank and vegetation, except for the seriously disturbed site. Our results suggest that the establishment of new species in severely disturbed areas is more dependent on the seed bank. By contrast, the restoration in less-disturbed and mature meadows does not rely on seed banks, and the establishment of the vegetation in these communities is more likely to rely on seed dispersal from the standing vegetation and on species with vegetative reproduction.