What determines the number and size of the seeds produced by a plant? How often should it reproduce them? How often should a plant produce them? Why and how are seeds dispersed, and what are the implications for the diversity and composition of vegetation? These are just some of the questions tackled in this wide-ranging review of the role of seeds in the ecology of plants. The authors bring together information on the ecological aspects of seed biology, starting with a consideration of reproductive strategies in seed plants and progressing through the life cycle, covering seed maturation, dispersal, storage in the soil, dormancy, germination, seedling establishment, and regeneration in the field. The text encompasses a wide range of concepts of general relevance to plant ecology, reflecting the central role that the study of seed ecology has played in elucidating many fundamental aspects of plant community function.

The ecology of seeds

Heightening human impacts on the Earth result in widespread losses of production and conservation values and make large-scale ecosystem restoration increasingly urgent. Tackling this problem requires the development of general guiding principles for restoration so that we can move away from the ad hoc, site- and situation-specific approach that now prevails. A continuum of restoration efforts can be recognized, ranging from restoration of localized highly degraded sites to restoration of entire landscapes for production and/or conservation reasons. We emphasize the importance of developing restoration methodologies that are applicable at the landscape scale. Key processes in restoration include identifying and dealing with the processes leading to degradation in the first place, determining realistic goals and measures of success, developing methods for implementing the goals and incorporating them into land-management and planning strategies, and monitoring the restoration and assessing its success. Few of these procedures are currently incorporated in many restoration projects. The concept that many ecosystems are likely to exist in alternative stable states, depending on their history, is relevant to the setting of restoration goals. A range of measures, such as those being developed to measure ecosystem health, could be used to develop “scorecards” for restoration efforts. Generalizable guidelines for restoration on individual sites could be based on the concepts of designed disturbance, controlled colonization, and controlled species performance. Fewer explicit guidelines are available at the landscape scale, beyond nonquantitative generalities about size and connectivity. Development of these guidelines is an important priority so that urgent large-scale restoration can be planned and implemented effectively.

Towards a Conceptual Framework for Restoration Ecology

Fire is a major modifier of communities, but the evolutionary origins of its prevalent role in shaping current biomes are uncertain. Australia is among the most fire-prone continents, with most of the landmass occupied by the fire-dependent sclerophyll and savanna biomes. In contrast to biomes with similar climates in other continents, Australia has a tree flora dominated by a single genus, Eucalyptus, and related Myrtaceae. A unique mechanism in Myrtaceae for enduring and recovering from fire damage likely resulted in this dominance. Here, we find a conserved phylogenetic relationship between post-fire resprouting (epicormic) anatomy and biome evolution, dating from 60 to 62 Ma, in the earliest Palaeogene. Thus, fire-dependent communities likely existed 50 million years earlier than previously thought. We predict that epicormic resprouting could make eucalypt forests and woodlands an excellent long-term carbon bank for reducing atmospheric CO2 compared with biomes with similar fire regimes in other continents.

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Flammable biomes dominated by eucalypts originated at the Cretaceous-Palaeogene boundary

Plant breeding and drought in C3 cereals: what should we breed for?

Resprouting as a response to disturbance is now widely recognized as a key functional trait among woody plants and as the basis for the persistence niche. However, the underlying mechanisms that define resprouting responses to disturbance are poorly conceptualized. Resprouting ability is constrained by the interaction of the disturbance regime that depletes the buds and resources needed to fund resprouting, and the environment that drives growth and resource allocation. We develop a buds-protection-resources (BPR) framework for understanding resprouting in fire-prone ecosystems, based on bud bank location, bud protection, and how buds are resourced. Using this framework we go beyond earlier emphases on basal resprouting and highlight the importance of apical, epicormic and below-ground resprouting to the persistence niche. The BPR framework provides insights into: resprouting typologies that include both fire resisters (i.e. survive fire but do not resprout) and fire resprouters; the methods by which buds escape fire effects, such as thick bark; and the predictability of community assembly of resprouting types in relation to site productivity, disturbance regime and competition. Furthermore, predicting the consequences of global change is enhanced by the BPR framework because it potentially forecasts the retention or loss of above-ground biomass.

https://nph.onlinelibrary.wiley.com/doi/pdf/10.1111/nph.12001

Resprouting as a key functional trait: how buds, protection and resources drive persistence after fire

Rice (Oryza sativa L) is an important staple crop that feeds more than one half of the world’s population and is the model system for monocotyledonous plants However, rice is very sensitive to salinity and is the most salt sensitive cereal crop with a threshold of 3 dSm−1 for most cultivated varieties Despite many attempts using different strategies to improve salinity tolerance in rice, the achievements so far are quite modest This review aims to discuss challenges that hinder the improvement of salinity stress tolerance in rice as well as potential opportunities for enhancing salinity stress tolerance in this important crop

https://www.mdpi.com/2073-4395/6/4/54/pdf

Improvement of salinity stress tolerance in rice: Challenges and opportunities

Available evidence suggests that there are at least two locations for dormancy mechanisms in primary dormant seeds: mechanisms based within the embryo covering structures, and mechanisms based within the embryo. Mechanisms within the covering structures may involve mechanical, permeability and chemical barriers to germination. Mechanisms within the embryo may involve the expression of certain genes, levels of certain plant growth regulators, the activity of important respiratory pathways or the mobilisation and utilisation of food reserves. In addition, some embryos may be too immature to germinate immediately and must undergo a further growth phase before germination is possible. An individual species could have one or several of these various dormancy mechanisms and these mechanisms need to be understood when selecting treatments to overcome dormancy. The way in which certain dormancy breaking agents are thought to work is discussed and practical applications of such agents in field situations are explained.

Seed dormancy mechanisms in warm season grass species

The effects of plant-derived smoke and of heat on the emergence of seedlings from seeds were assessed. Seeds had been stored in forest topsoil used for mine site rehabilitation. The study was carried out in a dry sclerophyll, spotted gum (Corymbia maculata), forest community at the Mount Owen open-cut coal mine in the Hunter Valley region of New South Wales. Samples of the surface 2.5 cm of topsoil were either exposed to cool smoke from eucalypt foliage for 60 min, heated to 80 degrees C, or left untreated. Seedling emergence from the seed bank in this soil was then monitored in a glasshouse. Within the first month, smoke alone promoted a 4.3-fold increase in the density of seedlings relative to control. There were 540 emergents per m(2) in the control and 2309 per m(2) in the smoke treated topsoil. Many annual and perennial herbs emerged but grasses responded most strongly to smoke. Germination in seven of the 20 grass species was promoted by smoke. Smoke promoted the germination of some introduced species as well as native species, and accelerated the rate at which seedlings emerged, although these differences sometimes declined with time. Heat also stimulated germination but smoke and heat stimuli appeared to be complementary in their promotion of seedling emergence from the topsoil seed bank. Each treatment increased the density of different species, enhanced the species richness of different components of the seed bank, and had different effects on the rate of emergence. The results suggest that increased seed germination in the field immediately following a moderate intensity fire may sometimes be the result of smoke stimulation and sometimes the result of heat stimulation of the soil seed bank. These findings may have important implications for minesite revegetation programs where topsoils are replaced after mining and rapid germination of seeds stored in these soils is required during short periods when conditions are favourable for germination.

Smoke and heat effects on soil seed bank germination for the re-establishment of a native forest community in New South Wales

The germination responses to plant-derived smoke of seeds of 20 native grass species from New South Wales, Australia, were tested under laboratory conditions. The species belonged to 14 genera including Bothriochloa, Chloris, Cymbopogon, Danthonia, Dichanthium, Digitaria, Eragrostis, Eriochloa, Microlaena, Panicum, Paspalidium, Poa, Stipa and Themeda. The interaction between smoke and husk-imposed dormancy was examined by removing the floral structures surrounding the seeds, when sufficient seeds were available. Smoke was shown to be an important environmental stimulus for breaking the dormancy of native grasses; however, the response differed considerably between different genera and between species of the same genus. For almost half of the species, smoke significantly increased the germination percentage. Panicum decompositum showed the greatest response, with germination increasing from 7.7 to 63.1% when smoke was applied. Panicum effusum had no germination in the absence of smoke, but 16.7% germination when smoke was applied. Stipa scabra subsp. scabra had germination significantly reduced by smoke from 30.2 to 19.9%. Five species had their germination rate, but not the final germination percentage, affected by smoke, and a third of the species were unaffected by smoke. For five of the species, Chloris ventricosa, Dichanthium sericeum, Panicum decompositum, Poa labillardieri and Stipa scabra subsp. falcata, this is the first report of a smoke-stimulated germination response. For those species with germination promoted by smoke, retention of the covering structures did not prevent smoke stimulation of germination. Sowing smoke-treated husked seeds is likely to be preferable as it would still promote greater germination, whereas dehusking seeds can result in the seeds being more susceptible to desiccation and fungal attack in the field. It is suggested that other grassland communities that respond to pyric conditions may also contain species that respond to smoke.

Smoke affects the Germination of Native Grasses of New South Wales

The germination responses of 10 species (Acacia blakelyi, A. pulchella, Allocasuarina humilis, Beaufortia elegans, Conostylis neocymosa, Eucalyptus tetragona, Kennedia prostrata, Leptospermum spinescens, Melaleuca acerosa and Xanthorrhoea drummondii) to constant temperatures ranging from 5 to 35o C were studied. These Western Australian perennial species had optimum germination percentages between 15 and 20oC, except Eucalyptus tetragona which had an optimum at 25oC and Leptospermum spinescens which had an optimum at 10°C. Seeds were transferred from high and low temperatures to 15oC to determine whether high or low temperatures induced dormancy. Low temperatures tended not to affect subsequent germination but high temperature decreased subsequent germination for some species. Wetting and drying stimulated the germination of Acacia blakelyi, A. pulchella and Kennedia prostrata seeds.

Sean M. Bellairs

Papers

Improvement of salinity stress tolerance in rice: Challenges and opportunities

Seed dormancy mechanisms in warm season grass species

Smoke and heat effects on soil seed bank germination for the re-establishment of a native forest community in New South Wales

Smoke affects the Germination of Native Grasses of New South Wales

Temperature effects on the seed germination of ten kwongan species from Eneabba, Western Australia.