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

Several hypotheses, mainly Optimal Defense (OD), Carbon:Nutrient Balance (CNB), Growth Rate (GR), and Growth‐Differentiation Balance (GDB), have individually served as frameworks for investigating the patterns of plant defense against herbivores, in particular the pattern of constitutive defense. The predictions and tests of these hypotheses have been problematic for a variety of reasons and have led to considerable confusion about the state of the “theory of plant defense.” The primary contribution of the OD hypothesis is that it has served as the main framework for investigation of genotypic expression of plant defense, with the emphasis on allocation cost of defense. The primary contribution of the CNB hypothesis is that it has served as the main framework for investigation of how resources affect phenotypic expression of plant defense, often with studies concerned about allocation cost of defense. The primary contribution of the GR hypothesis is that it explains how intrinsic growth rate of p...

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Out Of The Quagmire Of Plant Defense Hypotheses

http://www.noahwhiteman.org/uploads/7/1/3/1/7131048/trplsc952.pdf

Evolution of jasmonate and salicylate signal crosstalk.

Phenotypic plasticity is considered the major means by which plants cope with environmental heterogeneity. Although ubiquitous in nature, actual phenotypic plasticity is far from being maximal. This has been explained by the existence of internal limits to its expression. However, phenotypic plasticity takes place within an ecological context and plants are generally exposed to multifactor environments and to simultaneous interactions with many species. These external, ecological factors may limit phenotypic plasticity or curtail its adaptive value, but seldom have they been considered because limits to plasticity have typically addressed factors internal to the plant. We show that plastic responses to abiotic factors are reduced under situations of conservative resource use in stressful and unpredictable habitats, and that extreme levels in a given abiotic factor can negatively influence plastic responses to another factor. We illustrate how herbivory may limit plant phenotypic plasticity because damaged plants can only rarely attain the optimal phenotype in the challenging environment. Finally, it is examined how phenotypic changes involved in trait-mediated interactions can entail costs for the plant in further interactions with other species in the community. Ecological limits to plasticity must be included in any realistic approach to understand the evolution of plasticity in complex environments and to predict plant responses to global change.

https://nph.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1469-8137.2007.02275.x

Ecological limits to plant phenotypic plasticity

Allocation is one of the central concepts in modern ecology, providing the basis for different strategies. Allocation in plants has been conceptualized as a proportional or ratio-driven process (‘partitioning’). In this view, a plant has a given amount of resources at any point in time and it allocates these resources to different structures. But many plant ecological processes are better understood in terms of growth and size than in terms of time. In an allometric perspective, allocation is seen as a size-dependent process: allometry is the quantitative relationship between growth and allocation. Therefore most questions of allocation should be posed allometrically, not as ratios or proportions. Plants evolve allometric patterns in response to numerous selection pressures and constraints, and these patterns explain many behaviours of plant populations. In the allometric view, plasticity in allocation can be understood as a change in a plant's allometric trajectory in response to the environment. Some allocation patterns show relatively fixed allometric trajectories, varying in different environments primarily in the speed at which the trajectory is travelled, whereas other allocation patterns show great flexibility in their behaviour at a given size. Because plant growth is often indeterminate and its rate highly influenced by environmental conditions, ‘plasticity in size’ is not a meaningful concept. We need a new way to classify, describe and analyze plant allocation and plasticity because the concepts ‘trait’ and ‘plasticity’ are too broad. Three degrees of plasticity can be distinguished: (1) allometric growth (‘apparent plasticity’), (2) modular proliferation and local physiological adaptation, and (3) integrated plastic responses. Plasticity, which has evolved because it increases individual fitness, can be a disadvantage in plant production systems, where we want to optimize population, not individual, performance.

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Allocation, plasticity and allometry in plants

Induced Responses to Herbivory.

Effects of temperature on maturation of pseudothecia of Leptosphaeria maculans and L. biglobosa, closely related species which coexist on UK oilseed rape, were investigated. Stages in pseudothecial maturation on naturally infected oilseed rape debris were examined, both in controlled environments (5, 10, 15 or 20°C) under continuous wetness and in natural conditions (debris exposed in September and December 2000, and July, September and November 2002). Pseudothecia sampled weekly were assigned to maturation classes A (asci undifferentiated), B (asci differentiated), C (ascospores differentiated) or D (ascospores mature). Progress in pseudothecial maturation (assessed by time until 50% of pseudothecia reached each class) was similar for L. maculans and L. biglobosa at 15–20°C, but L. biglobosa matured more slowly at < 10°C. Maturation time decreased almost linearly with temperature from 5 to 20°C under continuous wetness but was longer in natural conditions, especially when periods of dry weather occurred. Differences in pseudothecial maturation are likely to contribute to epidemiological differences between L. maculans and L. biglobosa, which may explain their coexistence. It is appropriate to use the degree-day approximation to assess pseudothecial maturation at temperatures between 5 and 20°C, providing debris is wet.

Effects of temperature on maturation of pseudothecia of Leptosphaeria maculans and L. biglobosa on oilseed rape stem debris

Germination of native tree and shrub species from seed can be unpredictable. Germination of Rosa corymbifera ‘Laxa’ was 2% under normal commercial conditions. This was obtained in the presence of the natural microflora found on the seeds. The microflora originated on the hips and the seeds become inoculated during extraction. Exclusion of microbes from such pretreatments resulted in no germination. Inoculation of surface sterilized seeds with members of the natural microflora resulted in 3% germination. The addition of Garotta TM , a commercial compost activator, to the commercial pretreatment increased germination to 95%. This high germination percentage was sustained over a 5 year period using seeds from the same stock bushes. Addition of the compost activator resulted in a 20-fold increase of microbial activity in the pretreatment mixture, indicating that enhanced microbial growth resulted in higher and more predictable germination percentages.

https://www.cambridge.org/core/services/aop-cambridge-core/content/view/S0960258500000520

Microbial enhancement of seed germination in Rosa corymbifera ‘Laxa’

In China, the incidence of phoma stem canker observed in pre-harvest surveys from 2005 to 2012 was greater on winter oilseed rape in provinces in central China (in May) than on spring oilseed rape in north China (in August). In all 742 cases when the causal pathogen was isolated from stem cankers, it was identified as Leptosphaeria biglobosa by morphology in culture and/or by species-specific polymerase chain reaction. Both L. biglobosa and Leptosphaeria maculans were detected on crop debris and seed in shipments of oilseed rape seed imported into China through Shanghai or Wuhan ports in 2009–2011. Descriptions of the observed spread of L. maculans into areas previously colonized by L. biglobosa across a spring oilseed rape growing region (Alberta, Canada, westwards, 1984–1998) and across a winter oilseed rape growing region (Poland, eastwards, 1984–2004) were used to estimate the potential westward spread of L. maculans in China across spring oilseed rape growing regions (north China) and winter oilseed rape growing regions (central China, generally provinces along the Yangtze River), respectively. The rates of spread were estimated as 47 km per year across spring oilseed rape in north China and 70 km per year across winter oilseed rape in central China. Dispersal modelling suggested that the rate of spread of L. maculans across Alberta, Canada (c. 17 km per year) could be explained by windborne dispersal of ascospores.

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ppa.12146

Avice Hall

Papers

Induced Responses to Herbivory.

Effects of temperature on maturation of pseudothecia of Leptosphaeria maculans and L. biglobosa on oilseed rape stem debris

Microbial enhancement of seed germination in Rosa corymbifera ‘Laxa’

Leptosphaeria spp., phoma stem canker and potential spread of L. maculans on oilseed rape crops in China

Sequences of European wheat mosaic virus and oat golden stripe virus and genome analysis of the genus Furovirus