Scientists are becoming increasingly aware that disparities in opportunities for conducting and publishing research among scientists living under different socio-economic contexts have created pervasive biases and long-lasting impacts on our views of the natural world. These disparities are challenging the establishment of a global research agenda for a variety of disciplines, including seed ecology. Seed ecology has progressed enormously recently, but multiple barriers have hindered progress in the Global South where biodiversity and environmental complexity are highest. Here, we identify ten major challenges that seed ecologists from developing countries face in relation to planning, designing, conducting and publishing their research. We also propose several measures to overcome these challenges: (1) closing biodiversity knowledge shortfalls, (2) enhancing and creating long-term seed ecological networks, (3) supporting better infrastructure, (4) making fieldwork easier and safer, (5) unlocking funding opportunities, (6) promoting inclusive scientific meetings, (7) alleviating language barriers, (8) improving education, (9) shifting the notion of novelty and relevance and (10) supporting native seed markets. The authors recommend that the proposed solutions can be implemented by seed ecologists and the broader scientific community including funding agencies, research directors, journal editors and the academic publishing industry. Solutions can help mitigate multiple challenges simultaneously, thus offering a relatively inexpensive, fast and productive pathway for the development of seed ecology into a truly global research discipline that benefits scientists irrespective of their geographic location and background.

An in-depth understanding of the germination response of troublesome weed species, such as feather fingergrass (Chloris virgata Sw.), to environmental factors (temperature, soil moisture, etc.) could play an essential role in the development of sustainable site-specific weed control programs. A laboratory experiment was conducted to understand the germination response of 10 different biotypes of C. virgata to five temperature regimes (ranging from 15/5 to 35/25 C) under a 12/12-h (light/dark) photoperiod. No consistent germination behavior was observed between biotypes, as some biotypes demonstrated high final cumulative germination (FCG) at low alternating temperature regimes (15/5 and 20/10 C) and some biotypes exhibited high FCG at a high alternating temperature regime (30/20 C). All biotypes revealed late germination initiation (T10, time taken to reach 10% germination) at the lowest temperature range (15/5 C), ranging from 171 to 173 h. However, less time was required to reach 90% germination (T90), ranging from 202 to 756 h. At higher alternating temperature regimes (30/20 and 35/25 C), all biotypes initiated germination (T10) within 40 h, and a wide range of hours was required to reach 90% germination (T90), ranging from 284 to 1,445 h. Differences in FCG of all the biotypes at all the temperature ranges showcased the differential germination nature among biotypes of C. virgata. The cool temperatures delayed germination initiation compared with warmer temperatures, even though FCGs were similar across a wide range of thermal conditions, indicating that this species will be problematic throughout the calendar year in different agronomic environments. The data from this study have direct implications on scheduling herbicide protocols, tillage timing, and planting time. Therefore, data generated from this study can aid in the development of area- and species-specific weed control protocols to achieve satisfactory control of this weed species.

African lovegrass [Eragrostis curvula (Schrad.) Nees] is an invasive weed that is threatening biodiversity around the world and will continue to do so unless its efficient management is achieved. Consequently, laboratory and field-based experiments were performed to analyze several measures of germination to determine the effect of drought stress, radiant heat stress, and burial depth and duration (longevity) on E. curvula seeds. This study investigated seeds from four spatially varied populations across Australia: Maffra and Shepparton, VIC; Tenterfield, NSW; and Midvale, WA. Results showed that increasing drought stress reduced and slowed germination for all populations. Maffra (24% vs. 83%) and Shepparton (41% vs. 74%) were reduced at the osmotic potential of ≤−0.4 MPa, while Tenterfield (35% vs. 98.6%) and Midvale (32% vs. 91%) were reduced at ≤−0.6 MPa, compared with the mean of all other osmotic potentials. Radiant heat at 100 C significantly reduced and slowed germination compared with 40 C for Tenterfield (62% vs. 100%), Shepparton (15% vs. 89%), and Midvale (41% vs. 100%), while Maffra (75% vs. 86%) had consistent germination. For the effect of burial depth and duration (longevity), there was no significant difference across the 14-mo period; however, the 0-cm burial depth had a significantly lower final germination percentage compared with depths of 3, 5, and 10 cm (24% vs. 55%). Although each trial was conducted independently, the results can be used to help identify efficient control measures to reduce infesting populations. Recommended measures include using soil moisture monitoring to detect which conditions will promote germination, as germination is encouraged when the osmotic potential is >−0.6 MPa; exposing seeds to radiant heat (>100 C) using methods such as prescribed burning; and limiting soil disturbance over time to reduce seed establishment.

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.

For physiologically dormant (PD) species in fire-prone environments, dormancy can be both complex due to the interaction between fire and seasonal cues, and extremely deep due to long intervals between recruitment events. Due to this complexity, there are knowledge gaps particularly surrounding the dormancy depth and cues of long-lived perennial PD species. This can be problematic for both in situ and ex situ species management. We used germination experiments that tested seasonal temperature, smoke, dark and heat for 18 PD shrub species distributed across temperate fire-prone Australia and assessed how germination was correlated with environmental factors associated with their home environments. We found extremely high levels of dormancy, with only eight species germinating above 10% and three species producing no germination at all. Seven of these eight species had quite specific seasonal temperature requirements and/or very strong responses to smoke cues. The maximum germination for each species was positively correlated with the mean temperature of the source population but negatively correlated with rainfall seasonality and driest months. The strong dependence on a smoke cue for some of the study species, along with examples from other studies, provides evidence that an obligate smoke response could be a fire-adapted germination cue. Germination response correlated with rainfall season of the source populations is a pattern which has often been assumed but little comparative data across sites with different rainfall seasonality exists. Further investigation of a broader range of species from different rainfall season environments would help to elucidate this knowledge gap.

Establishment of seedlings of big sagebrush subsequent to range weed control treatments limits the economic feasibility of such treatments for increased forage production. This study investigated the dynamics of seed production by this species as one step in understanding seedling establishment. Studies were conducted on five different ecological sites along the arid extremity of big sagebrush distribution in western Nevada. Demography, physical dimensional parameters, biomass, and community structure were determined for each site and related to seed production over a 4-yr period. In addition, seeds harvested from each site were used to grow plants that were transplanted to establish reciprocal gardens at all sites. Seeds were subsequently harvested from the plants in these gardens. The average stand studied was capable of producing about 50 million seeds/ha annually. The plant characteristics most closely correlated with seed production were leaf weight, canopy density, and root crown diameter. The stand that consistently had the highest average seed production had the lowest woody biomass accumulation rate. In reciprocal gardens, plants grown from this stand had the highest average seed production. Seed production of big sagebrush plants appears to be related to site characteristics, shrub biomass characteristics, and inherent genetic potential of the plants in a given collection.

Experiments were conducted to compare the influence of production site and seed source on the germination of big sagebrush seeds in relation to incubation temperatures. Seeds of big sagebrush were collected from five plant communities located on the margin of the Carson Desert in western Nevada. Seedlings were grown from the seeds and transplanted back to the sites of collection in reciprocal gardens. Seeds from 1-yr-old gardens were tested for germination at a constant 15 C for three consecutive years. The greater quantity of seeds produced by 2- and 3-yr-old gardens were tested at 55 constant or alternating temperature regimes. Seeds of big sagebrush produced in reciprocal gardens had lower germination than seeds collected from native stands at the same locations. The reduced germination disappeared as the reciprocally transplanted plants grew older and larger, but seeds from these plants did not reach the same levels of germination as those collected from native stands at the same location. Moisture stress and/or freezing temperature conditions during flowering may have directly influenced the quality of seeds produced or interacted with the inherent genotypes of big sagebrush to trigger seed production of variable quality in relation to germination characteristics.

Dormant barnyardgrass seeds imbibed in darkness for 8 days at 38 C displayed a very low fluence response to phytochrome, and very little germination occurred in darkness. However, if seeds were imbibed at temperatures >42 C or exposed to 46 C for only 0.5 h, considerable germination was evoked in the absence of a light stimulus. It is proposed that the high temperatures caused a transition in dormancy from a light-requiring to a light-independent state. The finding may have relevance to field behavior of barnyardgrass seeds where burial could prevent reception of the required light stimulus.

Broom snakeweed achene dispersal was monitored by placing surface-level traps outwards in the cardinal directions from 12 plants and collecting the achenes weekly or biweekly from September 1993 until seeds were no longer retained by the plants after 42 wk. About 50% of the achenes dispersed between October and December. Especially high numbers of achenes were dislodged during periods of intense winter winds and rains, with 78% of the seed placed into the east tray and 86% falling within 50 cm of the parent plant. Achene production averaged 3,928 (± 1,146) per plant in 1993 and 2,036 (± 987) per plant in 1994. Achenes collected over time directly from the inflorescence and achenes stored in nylon packets on the soil surface averaged 82% viability during fall and winter. Achene viability declined rapidly in late spring, and few remained viable before the next seed crop. Greenhouse experiments compared the influence of water application interval and water amount on broom snakeweed germination and seedling survival. Treatments consisted of 4 water intervals: daily, 5-d, 10-d, and 15-d intervals; and 4 water amounts: field capacity (1/1 fc), 3/4 fc, 1/2 fc, and 1/4 fc. Germination was 52% at daily 1/1 fc, and no seed germinated at daily 1/4 fc. Data suggest that optimum germination occurs when soils are maintained at a minimum soil matric potential (Ψm) > −180 kPa for at least 4 d. Optimum Ψm for seedling survival appears to range between −300 and −900 kPa, while seedling mortality would generally be expected with a Ψm of > −1800 kPa.

Adaptive plastic responses in invasive species allow for establishment and persistence despite the lack of genetic matching to new environments. The capacity of annual species to invade habitats to which they are not adapted is likely to be predicated on post-invasion seed trait variation correlated with conditions in the new habitat. To test this, I compared variation in seed traits and germination patterns of Aegilops triuncialis, an invasive annual grass, from 69 sample populations from 24 sites in California (USA) across 13 years. Seed mass, germination fractions, seed viability, and strength of induced dormancy between dimorphic seed pairs were used to investigate plastic variation within and among populations, across two general soil types, and among two widespread maternal genotypes. I found that seed mass variation was constrained although both seed types showed a 3-fold range among populations, 20–25% variation within populations between years, and was positively correlated with longer growing seasons. However, induced seed dormancy in the small seed type was correlated with large seed mass and to late-season precipitation, suggesting that longer growing seasons influence the strength of maternal and sibling chemical signals that induce dormancy in the small seeds. Thus variation in small seed germination fractions varies with the growing conditions experienced by the maternal plant. The greater longevity of the small seed type suggests that plasticity in germination in this species may contribute to seed bank formation, which is atypical of invasive annual grasses in California, and this may contribute to the persistence and spread of A. triuncialis in invaded ranges.

Broom snakeweed is a native weed widely distributed on rangelands of western North America. It often increases to near monocultures following disturbance from overgrazing, fire, or drought. This paper presents an up-to-date review of broom snakeweed toxicology, seed ecology, population cycles, succession, and management. The greatest ecological concern is that broom snakeweed displaces desirable forage for livestock or wildlife and greatly reduces biodiversity. It also is toxic and can cause abortions in all species of livestock. Propagation usually is pulse-driven in wet years, allowing large expanses of even-aged stands to establish and dominate plant communities. Snakeweed can be controlled by prescribed burning or spraying with herbicides. A weed-resistant plant community dominated by competitive grasses can prevent or minimize its reinvasion.

Anatomical and morphological seed traits are of great ecological importance and are a main subject of, for example, seed bank or endozoochory studies. However, we observed a lack of information about the relationship between seed anatomy and seed morphology and its ecological implications. To fill this gap, we linked the anatomical features of diaspore coverings to morphological characteristics of free seeds and one-seeded fruits. We predicted that: (1) the thickness and anatomical complexity of seed coat and pericarp are related to diaspore size and shape; and (2) the presence or absence of the pericarp may influence seed-coat thickness and anatomy. In our study we investigated diaspores of 39 central-eastern European herbaceous species and recorded the thickness and anatomical complexity of their seed coverings, and we determined diaspore mass and shape. Our results indicate that diaspore mass is positively related to covering thickness, lignification degree and anatomical complexity. This might be the case because bigger diaspores tend to remain on the soil surface and are more exposed to predation risk and environmental threat than smaller diaspores. Furthermore, more round-shaped diaspores had disproportionately thicker and more lignified coverings than long or flat ones, probably because round-shaped diaspores much more frequently form seed banks and therefore persist for a long time in the soil. We also found that free seeds as diaspores have a thicker and more lignified seed coat than seeds enclosed in fruits. In one-seeded fruits, the pericarp ‘takes the protective role’, it is thick, and the seed coat is poorly developed.

Phenotypic plasticity in seed dormancy may allow plant species to cope with rapid environmental changes, such as climate warming. In controlled experimental settings, plasticity in dormancy has been found to relate to temperature during seed maturation, but this relationship has not been tested in field conditions. Here we analyse for the first time the variation in dormancy during five successive years in wild populations of the study species Centaurium somedanum, to determine how this variation is related to average temperatures during specific seasons of plant activity. We performed laboratory germination experiments to measure: (1) the degree of dormancy at dispersal; and (2) the sensitivity to dormancy-breaking factors. We calculated average temperatures during four seasons of plant activity (overwintering, vegetative growth, flowering and seed maturation) for each year, and tested the relationship between these temperatures and patterns of dormancy variation, using Generalized Linear Models. Dormancy varied among sites and years, seeds being more dormant in colder years. For the degree of dormancy at dispersal, we found a positive relationship with flowering temperature and a significant effect of collection site. For the sensitivity to dormancy-breaking factors, we found no significant differences among sites, a positive relationship with flowering temperature and a negative relationship with overwintering temperature. Phenotypic plasticity in dormancy in C. somedanum is thus especially marked in the sensitivity to dormancy-breaking factors. Temperatures during overwintering and flowering have differential effects on this plasticity, allowing the plant to detect the gradient of seasonality, a main ecological feature of its distribution. These results highlight the importance of taking into account more than average temperatures when assessing the response of plant phenotypic plasticity to climate change.

Seeds of Dodonaea viscosa (Sapindaceae) have a water-impermeable seed coat, i.e. physical dormancy (PY). Although mechanical scarification, dry heat, sulphuric acid and hot water treatment make seeds permeable under laboratory conditions, the mechanisms by which dormancy is alleviated in natural environments have not yet been understood completely. The present investigation aims to understand the pattern of dormancy alleviation in D. viscosa seeds using an artificial burial approach for 2 years. Freshly collected seeds held in hydrated soil at 10/20°C, 15/20°C, 15/30°C, 20/35°C and 25°C for 32 weeks germinated to less than 15%, irrespective of storage temperature. Dry storage of seeds at 15, 20, 25 and 30°C for 1 year did not break dormancy. Hot water treatment at 80 and 90°C for 30 s broke dormancy in 90% of the seeds. On the other hand, burying seeds at a depth of 3–5 cm in the natural environment for 2 years increased germination from 7 to 71%. In particular, seeds exhumed after summer in both years showed a significant increase in germination percentage (P< 0.05). However, seeds buried after summer did not germinate to a higher percentage when exhumed prior to summer. We suggest that a high summer temperature, rising above 60°C in the top soil layer of the tropics, is a likely factor breaking dormancy. Most seeds germinated during burial, which indicates that light is not a cue for germination. We conclude that germination of D. viscosa following summer is an adaptive mechanism to tolerate summer droughts, which are common in the dry tropics.

A large fraction of tree species forming persistent soil seed-banks and with dormant seeds are expected to be found in strongly seasonal ecosystems such as Neotropical savannas, where seedling recruitment could be highly variable. In the savannas of Central Brazil, we studied seed characteristics (type of dormancy, longevity and moisture content) of 14 representative woody species differing in seed dispersal season. We also studied the dynamics of soil seed-banks and similarity patterns in woody species composition among seed rain, soil seed-bank, seedling bank and standing vegetation along shallow topographic gradients that differ in canopy cover. Woody species composition of the soil seed-bank largely differed from the standing vegetation, the seed rain and the seedling bank species composition, suggesting low recruitment of woody species from the soil seed-bank. Seeds of the 14 woody species remained viable for less than 16 months in laboratory dry-storage conditions. Of those, most seeds dispersed in the dry season were dormant and exhibited low moisture content, while most seeds dispersed in the wet season were non-dormant and exhibited high moisture content. Longevity of these seeds dispersed in the dry and the wet seasons did not differ significantly. This study shows that both timing of seed dispersal and dormancy appear to control timing of seed germination and seedling recruitment of most Neotropical savanna woody species, which did not form persistent soil seed-banks. This study contributes to the understanding of tree/grass coexistence and tree density variations along topographic gradients in tropical savannas.

Secondary dormancy is predominantly associated with seed behaviour in soil seed banks. Periodic changes in secondary dormancy may explain seasonal emergence of weedy species. Temperature and possibly soil water potential appear to be the predominant factors that determine the annual cycling of dormancy. Dormancy cycling is paralleled by modulations of germination responsiveness to germination stimulants, such as light and nitrate and to the width of the germination temperature window. Membranes have been proposed to be the primary target for the perception of temperature. It is hypothesized that alterations in properties of cellular membranes are involved in the regulation of dormancy. Possible mechanisms are discussed.

This is the first report on the SEed Ecological Database (SEED) being developed under the co-ordination of the author. In its first version the database will cover physical characteristics of seeds, such as: slenderness (length/width), flatness (thickness/width) and thousand-seed weight. The list of species encompasses all seed plants (gymnosperms and angiosperms) native or naturalized in Hungary (about 2450 species). Two examples to demonstrate the power of SEED are included. The significantly lower slenderness values of Hungarian C4 grasses (compared with C3 types), shown in the first example, is a new contribution to understanding the ecology of C4 grasses. In the second example heavier seed weights of shade plants are statistically demonstrated, compared to their heliophilous congeners with the same life forms. The 113 congeneric species pairs considered are derived from a wide range of plant families.

This is the first study to determine the class of seed dormancy (or non-dormancy) of a large number of native tree species in a tropical forest, the seasonal moist tropical forest of the Panama Canal Watershed (PCW), or to test the relationships between class of dormancy (or non-dormancy) and various seed and ecological characteristics of the constituent species. Fresh seeds of 49 of 94 tree species were non-dormant (ND), and 45 were dormant (D). Seeds of 23 species had physiological dormancy (PD), 13 physical dormancy (PY), two morphological dormancy (MD), 7 morphophysiological dormancy (MPD) and none combinational dormancy (PY+PD). Seeds with PY were significantly smaller ( < 0.1 g) and drier (moisture content < 16%) at maturity than those that were ND or in the other D classes. Seeds of 62, 42 and 53% of species dispersed in the early rainy, late rainy (LRS) and dry seasons, respectively, were ND. The majority (61%) of species with PD seeds, but only 17% of those with PY seeds, were dispersed in the LRS. The proportion of species with ND seeds was higher in large-size (63%) than in mid-size (35%) and understorey (17%) trees, but differed only slightly between non-pioneers (58%) and pioneers (54%). The proportion of species with D seeds increased only slightly through a precipitation gradient of about 3100 to 1900 mm in the PCW; however, PY increased from 19 to 32% and PD decreased from 63 to 44%.

Nitrates have long been known to promote seed germination in many species, and various proposals have been made regarding the role of nitrates in this process. One hypothesis suggests a possible ecological role for nitrate, providing the seeds with a report of soil nitrogen status and the proximity of already established plants. However, nitrogen oxides (NO, NO2), which are present in the soil, also may be information carriers that indicate not only soil nitrate content, but also microbial activity and, therefore, soil quality. Because of annual variation of soil trace gas fluxes, seeds could be provided with information on seasonal and climate changes in their surroundings. Thus, nitrogen oxides would be the outer information carriers providing the seeds with integral data about many important factors required for successful germination and seedling establishment.