Seed conservation of banana crop wild relatives (Musa L. spp.) is limited because of lack of knowledge about their germination ecology. Musa acuminata Colla, the most important banana crop wild relative, is distributed in tropical and subtropical Asian and Pacific rainforests and colonizes disturbed sites. The role of temperature in stimulating/inhibiting germination to detect disturbance when canopy gaps are formed is not well known. We assessed seed germination thermal requirements of three subspecies of M. acuminata using nine seed accessions which had been stored in the Millennium Seed Bank. Diurnally alternating temperature cycles were almost completely essential for germination compared with constant temperatures. Germination was optimal when the upper temperature of a diurnal cycle was at 35°C; the lower temperature of the cycle was less important. Subspecies occurrence coordinates were used to extract climate temperature data which were then compared against the temperature requirements for germination from our experiment results. Maximum temperatures of the warmest month across subspecies ranges were close to but below optimal germination temperatures, as were diurnal ranges, suggesting soil-warming at the micro-climate level following gap creation is important for M. acuminata seed germination. Additionally, pre-treatment for 3 months at 60% relative humidity at constant 25°C improved germination from 14 ± 10 (mean, standard deviation) to 41 ± 29% suggesting a period in the soil seed bank under the canopy may increase sensitivity to alternating temperature cycles. Overall viability was low (49 ± 28%), and considerable variance was caused by the different accessions. Germination remained somewhat inconsistent.

The influence of temperature and water availability on seed germination can vary across the geographic range of species with a large distribution. Betula pendula is a widely spread European tree that has differentiated into two narrowly distributed taxa, endemic to Mediterranean mountains: Betula aetnensis in Sicily and B. fontqueri in Spain and Morocco. We tested the hypothesis that the regeneration niche, expressed by temperature and water potential thresholds, varies across these species and is influenced by the local climate. Seeds were collected from six populations of B. pendula, one of B. fontqueri and two of B. aetnensis. Germination tests were conducted between 5 and 30°C. The thermal thresholds were calculated before and after cold stratification. The osmotic potential tested ranged from 0 to −1.5 MPa. Time to reach 30 and 50% of germination was calculated by fitting non-linear models. Germination was promoted by high temperatures, but the response to stratification was heterogeneous. Tb and Ψb differed between and within species. Tb ranged between 2.22 and 8.94°C for unstratified seeds. Mediterranean species had higher drought tolerance, while B. pendula showed contrasting responses to low water potential. Ψb reached a minimum value of −1.15 MPa in B. fontqueri. High temperatures influenced the Tb of unstratified seeds negatively, while, after stratification, the Tb increased with precipitation in the driest month. The heterogeneity observed could reflect higher genetic variability in marginal populations of silver birch. Knowledge of their germination ecology may be useful to mitigate future impacts of climate change on core populations of B. pendula.

In wetlands, dormancy may be a key functional trait enabling seeds to avoid underwater germination, which could be lethal for seedling establishment. Our objectives were to find out (i) if shallow dormant (i.e. conditionally dormant) Echinochloa crus-galli seeds from an anaerobic germination resistant accession can break dormancy under hypoxic submergence and (ii) if underwater germination can be restored in scarified, non-dormant seeds. Shallow dormant E. crus-galli seeds perceived diurnally alternating temperatures (AT) and red light (R) pulses (i.e. dormancy-breaking cues) under hypoxic submergence; however, an inhibitory far-red light pulse given at the end of the 4-d inundation period demonstrated that most of the seeds (85%) were unable to break dormancy. Scarified E. crus-galli seeds, which did not express dormancy under drained conditions, were unable to germinate under hypoxic submergence, despite being exposed to dormancy-breaking cues (AT + R). Lastly, the temporal window for germination sensitivity to the inhibitory action of hypoxia, once dormancy-breaking signals have been applied, is progressively lost and bounded to approximately 18 h for half of the seed lot. These results highlight the importance of dormancy as a trait enabling E. crus-galli seeds to avoid underwater germination, a risky scenario for seedling emergence and establishment in this facultative hydrophyte.

Mudflats are exposed for short periods after flood water drawdown. They support fast-growing annual herbs with a ruderal strategy. To optimize their recruitment success, seeds of mudflat species germinate better under fluctuating temperatures, full illumination and aerobic environments that indicate the presence of optimal (non-flooded) conditions for plant growth and development. Here, we hypothesize that prior exposure of mudflat seeds to hypoxic (flooded) environment interferes with the germination process and results in more vigorous germination once aerobic conditions are regained. To test this hypothesis, seeds of five mudflat species were incubated in both aerobic and hypoxic environments at four (14/6, 22/14, 22/22 and 30/22°C) temperature regimes, reflecting different (seasonal) conditions when drawdowns may occur. All species responded positively to four temperature regimes; however, moderate 22/14 and 22/22°C temperatures were optimum for high percentages and rates (speed) of seed germination. Since seeds of four species germinated exclusively under aerobic conditions, they were moved from hypoxic to aerobic conditions. Prior exposure of seeds to hypoxic environment facilitated high percentages, rates and synchronization of germination of Limosella aquatica, Peplis portula and Samolus valerandi seeds compared to incubation under strict aerobic conditions. However, prior exposure to hypoxic environment induced secondary dormancy in non-dormant seeds of Hypericum humifusum but broke dormancy in Lythrum hyssopifolia seeds that otherwise required cold stratification to overcome physiological dormancy. All species that have a narrow ecological niche (strictly occurring in mudflat habitats) showed positive responses to prior exposure to hypoxic environments. In contrast, H. humifusum that has a wide ecological niche (from mudflats to moist sandy grasslands) showed a negative response. We conclude that the hypoxic environment may strongly affect seed germination behaviour once the aerobic environment is regained. The most striking effect is the acceleration of the germination process and, therefore, life cycle supporting the survival in an ephemeral habitat.

Fire is a frequent disturbance in the Cerrado and is one of the major factors affecting vegetation structure and diversity. Fire events open gaps within the herbaceous layer and increase temperature fluctuation in the soil surface. In addition to being an important environmental filter for germination, fire is a germination cue for species with physiological dormancy. This study aimed to evaluate the germination of native grasses, using daily temperature fluctuations and heat shock to overcome physiological dormancy in native grasses. We also evaluated seed longevity after dispersal for some species. We conducted the daily temperature fluctuation experiments on seeds of ten native grass species, which were collected and then placed in germination chambers simulating thermal fluctuation throughout the day (19–55°C). We also subjected seeds to different heat-shock treatments: 100°C for 1 min, 100°C for 3 min and 200°C for 1 min. To determine seed longevity, we stored seeds for 6 and 12 months after collection and then set them to germinate (27°C, 12/12 h light). Non-germinated seeds from all experiments were tested for viability. Most species had low longevity and germination percentages. Those that had physiological dormancy were stimulated to germinate when exposed to temperature fluctuations. One species resisted temperatures up to 200°C. For all other species, neither treatment affected germination percentages. Our results indicate the importance of these environmental filters for seedling recruitment of these species, considering the low longevity and the presence of physiological dormancy.

We hypothesized that Strychnos nux-vomica and Strychnos potatorum in seasonal tropical ecosystems have dormant desiccation-tolerant seeds, while those of Strychnos benthamii growing in aseasonal wet habitats have non-dormant desiccation-sensitive seeds. Germination, imbibition, the effect of gibberellic acid on germination and changes in the embryo to seed length ratio (E:S) during incubation were determined for the three species. Seed storage behaviour was identified with the hundred seed test. Time taken for epicotyl emergence was recorded. Radicle emergence of S. nux-vomica, S. potatorum and S. benthamii at 25°C under light/dark conditions (12/12 h) was completed within 76, 49 and 11 d, respectively. S. nux-vomica and S. potatorum seeds incubated on GA3 germinated to a higher percentage than non-treated seeds. E:S of S. nux-vomica, S. potatorum and S. benthamii had increased by 38.2, 34.5 and 25.5%, respectively, at radicle emergence. Shoot emergence of S. nux-vomica, S. potatorum and S. benthamii was observed after 76, 74 and 45 d from radicle emergence, respectively. Thus, it can be concluded that the seeds of all three species have epicotyl morphophysiological dormancy. Hundred seed tests revealed that S. nux-vomica and S. potatorum seeds were desiccation-tolerant, while those of S. benthamii were desiccation-sensitive. Our study showed that species from seasonal habitats (S. nux-vomica and S. potatorum) have desiccation-tolerant morphophysiologically dormant seeds, while those from an aseasonal habitat (S. benthamii) have desiccation-sensitive morphophysiologically dormant seeds, revealing that their dormancy and desiccation tolerance behaviour are adaptations to their environment.

Using seeds to restore natural ecosystems has a greater chance of success if the seeds used are ready to germinate given appropriate environmental conditions. For Australian native Poaceae species, seed quality and dormancy can impose constraints on restoration success. In this study, germination biology of three Australian native Poaceae species, such as Cymbopogon refractus, Capillipedium spicigerum and Bothriochloa bladhii, was investigated. The seeds were exposed to different germination-enhancing chemicals (GECs, namely smoke water (SW), potassium nitrate (KNO3) or a combination (SW + KNO3)) and treated with three different seed enhancement technologies (SETs, namely seed priming, seed coating or seed cookies) then sown into two contrasting soil types (sodosol or black vertisol). Laboratory germination percentages achieved were <50% for all species, limited by dormant seeds. Incorporating GECs together with seed priming or seed coating treatment significantly increased seedling emergence rates and promoted earlier emergence as compared to the untreated control. For C. refractus and C. spicigerum, priming and/or coating with KNO3 + SW had the highest cumulative emergence. For B. bladhii, total seedling emergence was the highest (36% in both soils) for primed seeds with KNO3. Seedling emergence from seed cookies was low in all three species (<15%). Generally, soil type did not influence emergence rates for either GEC or SET. Understanding the environmental requirements needed for seed germination, together with an appropriate pre-treatment before sowing, can speed up seedling emergence and increase total emergence when using native Poaceae species for seed-based restoration.

Seed dispersal has key implications for community dynamics and restoration ecology. However, estimating seed rain (the number and diversity of seeds arriving in a given area) is challenging, and the lack of standardization in measurement prevents cross-site comparisons. Seed trap effectiveness and accuracy of seed sorting methods are key components of seed rain estimates in need of standardization. We propose and describe a standardized protocol for evaluating the effectiveness of two seed trap types (sticky and funnel traps) and the accuracy of a seed sorting method. We used widely available seeds (arugula, quinoa, sesame and sunflower) to produce a gradient of seed size, weight and colour. Proof-of-concept was tested in a tropical grassland, where traps were set for 30 days. Our results suggest that we underestimate dispersal of seeds with less than 2 mm width that can be easily mistaken for debris and soil particles or that fail to adhere to sticky traps. Seeds on sticky traps may be more vulnerable to removal by wind and rain, whereas seeds in funnel traps are more susceptible to decay. We found no evidence of observer bias on seed sorting for funnel trap samples. However, accuracy on seed sorting for funnel trap samples tended to decline for seeds with less than 2 mm width, suggesting a size-dependence in seed retrieval success. Our standardized protocol addressing trap effectiveness and seed sorting methods will increase the reliability of data obtained in seed rain studies and allow more reliable comparisons between datasets.

Interception by plant canopies during wind dispersal can affect the final destination of diaspores. However, how the interaction of wind speed, canopy type and diaspore attributes affects interception of diaspores by the plant canopy has rarely been studied. We investigated canopy interception for 29 species with different diaspore attributes, six canopy types and six wind speeds in controlled experiments in a wind tunnel. Shrub canopy interception of diaspores were controlled by wind speed and diaspore attributes, but the latter had a greater influence on canopy interception than the former. At low wind speed, diaspore wing loading had a large influence on canopy interception, whereas at high wind speed, diaspore projection area had a large influence. The chance of canopy interception at a particular wind speed was additionally affected by the type of canopy. This study increases our knowledge of the dispersal process, corrects the previous understanding of diaspore dispersal potential and improves the theoretical basis for predicting spatial pattern and dynamics of plant populations.

Cultivated rice (Oryza sativa L.) was domesticated from the Asian wild species O. rufipogon. Compared with cultivated rice, wild rice has spikelets/seeds with long barbed awns. In order to evaluate the role of awns in wild rice, four seed groups with different awn lengths (full, half, quarter and no awns) were prepared, and the following seed dispersal movements were investigated under simulated natural conditions as observed in the tropical Asian habitat: (1) seed detachment from the parent plant; (2) falling angle of mature seed; (3) ability to slip into small spaces; (4) horizontal movement on the ground and (5) horizontal movement in water. As a result, awns were found to enhance the detachment of matured seeds from the panicles in the initial seed dispersal step. They regulated vertical orientation in the air, and the vertical form may enable seeds to squeeze to the ground. The awned seeds also showed advantages in horizontal movements on the ground and in the water. In most of the experiments, seeds with full awns showed the best performance for seed dispersal, suggesting that wild rice keeps long awns to survive under natural conditions. Since seed awning is dominantly controlled by wild functional alleles at several loci, wild rice may be able to prevent a drastic reduction of awn length.