Search

Ecologically meaningful seed germination experiments are constrained by access to seeds and relevant environments for testing at the same time. This is particularly the case when research is carried out far from the native area of the studied species.Here, we demonstrate an alternative—the use of glasshouses in botanic gardens as simulated‐natural habitats to extend the ecological interpretation of germination studies. Our focal taxa were banana crop wild relatives (Musa acuminata subsp. burmannica, Musa acuminata subsp. siamea, and Musa balbisiana), native to tropical and subtropical South‐East Asia. Tests were carried out in Belgium, where we performed germination tests in relation to foliage‐shading/exposure to solar radiation and seed burial depth, as well as seed survival and dormancy release in the soil. We calibrated the interpretation of these studies by also conducting an experiment in a seminatural habitat in a species native range (M. balbisiana—Los Baños, the Philippines), where we tested germination responses to exposure to sun/shade. Using temperature data loggers, we determined temperature dynamics suitable for germination in both these settings.In these seminatural and simulated‐natural habitats, seeds germinated in response to exposure to direct solar radiation. Seed burial depth had a significant but marginal effect by comparison, even when seeds were buried to 7 cm in the soil. Temperatures at sun‐exposed compared with shaded environments differed by only a few degrees Celsius. Maximum temperature of the period prior to germination was the most significant contributor to germination responses and germination increased linearly above a threshold of 23℃ to the maximum temperature in the soil (in simulated‐natural habitats) of 35℃.Glasshouses can provide useful environments to aid interpretation of seed germination responses to environmental niches., Seeds of wild banana species germinate in response to subtle changes in temperature dynamics as found in direct exposure to the sun rather than in shade and are less tuned to temperature changes associated with burial depth. Results were obtained from experiments in environments used as proxies to natural habitats (glasshouses and a plant nursery). Methods are presented to aid interpretation of seed germination studies when access to natural environments is not possible.

Resurrecting extinct species is a fascinating and challenging idea for scientists and the general public. Whereas some theoretical progress has been made for animals, the resurrection of extinct plants (de-extinction sensu lato) is a relatively recently discussed topic. In this context, the term 'de-extinction' is used sensu lato to refer to the resurrection of 'extinct in the wild' species from seeds or tissues preserved in herbaria, as we acknowledge the current impossibility of knowing a priori whether a herbarium seed is alive and can germinate. In plants, this could be achieved by germinating or in vitro tissue-culturing old diaspores such as seeds or spores available in herbarium specimens. This paper reports the first list of plant de-extinction candidates based on the actual availability of seeds in herbarium specimens of globally extinct plants. We reviewed globally extinct seed plants using online resources and additional literature on national red lists, resulting in a list of 361 extinct taxa. We then proposed a method of prioritizing candidates for seed-plant de-extinction from diaspores found in herbarium specimens and complemented this with a phylogenetic approach to identify species that may maximize evolutionarily distinct features. Finally, combining data on seed storage behaviour and longevity, as well as specimen age in the novel 'best de-extinction candidate' score (DEXSCO), we identified 556 herbarium specimens belonging to 161 extinct species with available seeds. We expect that this list of de-extinction candidates and the novel approach to rank them will boost research efforts towards the first-ever plant de-extinction.

We reviewed the status of orthodox seed collections of globally threatened plants conserved in − 20 °C long-term storage at the Millennium Seed Bank, Royal Botanic Gardens, Kew, UK in terms of their geographic and bioclimatic representativeness, taxonomic and genetic diversity, quality and physiological status. The comprehensive dataset used spans over 45 years of worldwide conservation effort across various organisations. The data provides evidence-based results and future directions for the represented globally threatened flora that are of relevance to all plant conservation and seed banking organisations across the globe. The reviewed sample includes 523 collections and represents a wide geographic range, originating from 67 countries, from all nine bio-geographic continents. The majority of collections originated from temperate climates and from habitats with no dry seasons but experiencing warm summer periods. The taxonomic composition of the collections highlighted a substantial diversity, with 303 taxa (four extinct in the wild; 56 critically endangered; 105 endangered; and 138 vulnerable) represented by 297 species, 199 genera and 74 families. Almost four fifths of the collections were harvested from wild habitats. Whilst wild-origin collections can harbour useful genes not available in the cultivated gene pool, for threatened plants both collections and taxa are likely to suffer from low genetic diversity as a low number of individual plants, populations and/or potentially viable or usable seeds were sampled at the original harvest. Large numbers of empty and infested seeds in the original harvest have significantly affected the quality of collections in terms of availability of potentially viable or usable seeds in collections. As a result, just over one third of taxa and one fifth of collections consisted of ≥ 5000 potentially viable or usable seeds. Viable seeds exhibited a sound physiological status in terms of germinability and viability at the initial round of germination tests after storage, but on average, relative germination and viability achieved were below 85%. A decline in germinability during their variable time of storage was evident for 16% of the 78 collections analysed for longevity. According to a set of criteria, suitable germination protocols for propagation of plants from seeds were identified for 165 taxa. Given the apparent differences between wild species, especially those that are rare and threatened, and domesticated crops, the quality and physiological status of reviewed collections are reasonably sound. The characteristics we observed for collections, the challenges we identified for conserving them and the germination protocols we suggested for propagation of plants from seeds have the scope to be noted, integrated and used globally across various conservation activities and policies.

Seed coat and seed reserve show substantial mass variation, play different roles in plant life strategies and are shaped by different selective forces. However, remarkably little is known about the macroevolution of the relative allocation in seed components and its influence on important ecophysiological processes. Using phylogenetic comparative methods and evolutionary modelling approaches, we modelled mass changes in seed components along individual lineages for 940 species and compared the patterns across seed desiccation responses. Seed component allocation was driven primarily by changes in reserve mass rather than coat mass, as evolutionary rates in reserve mass significantly outpaced those in coat mass. Although the scaling patterns between reserve mass and coat mass were similar across desiccation responses, desiccation-sensitive seeds allocated more and evolved faster in reserve compared to desiccation-tolerant seeds. The findings emphasize the relative importance of reserve to coat in the evolution of plant reproductive strategies, revealing potential ecological advantages gained by enlarged reserve. As the first quantification of the evolutionary tempo and mode of seed component mass, our study allows a detailed interpretation of evolutionary pathways underlying seed storage behaviours and advances the understanding of the evolution of desiccation sensitivity in seeds.

UK trees require increased conservation efforts due to sparse and fragmented populations. Ex situ conservation, including seed banking, can be used to better manage these issues. We conducted accelerated ageing tests on seeds of 22 UK native woody species, in order to assess their likely longevity and optimize their conservation in a seed bank. Germination at four ageing time points was determined to construct survival curves, and it was concluded that multiple samples within a species showed comparable responses for most species tested, except for Fraxinus excelsior. Of all species studied, one could be classified as very short-lived, four as short-lived and 17 as medium, with none exceeding the medium category. The most important finding of this manuscript is that although some taxonomic trends were observed, the results indicate the need for caution when making broad conclusions on potential seed storage life at a species, genus or family level. Longevity predictions were compared to actual performance of older collections held in long-term storage at the Millennium Seed Bank, Kew. Although most collections remain high in viability in storage after more than 20 years, for short-lived species at least, there is some indication that accelerated ageing predicts longevity in seed bank conditions. For species with reduced potential longevity, such as Fagus sylvatica and Ulmus glabra, additional storage options are recommended for long-term gene banking.

Storing seed collections of crop wild relatives, wild plant taxa genetically related to crops, is an essential component in global food security. Seed banking protects genetic resources from degradation and extinction, and provides material for use by breeders. Despite being amongst the most important crops in the world, banana and plantain crop wild relatives are largely under-represented in gene banks. Nevertheless, banana crop wild relative seed collections are in fact held in different countries, but these have not previously been part of reporting or analysis. To fill these gaps, we firstly collated data from 13 institutions in 10 countries. These included 537 accessions containing an estimated 430,000 seeds of 56 species. We reviewed their taxonomic coverage and seed storage conditions including viability estimates. We found that seed accessions have low viability (25% mean) representing problems in seed storage and processing. Secondly, we surveyed 22 institutions involved in banana genetic resource conservation regarding key constraints and knowledge gaps that institutions face related to banana seed conservation. Major constraints were identified including finding suitable material and populations to collect seeds from, lack of knowledge regarding optimal storage conditions and germination conditions. Thirdly, we carried out a conservation prioritization and gap analysis of Musaceae taxa, using established methods, to index representativeness. Overall, our conservation assessment showed that despite this extended data set banana crop wild relatives are inadequately conserved, with 51% of taxa not represented in seed collections at all; the average conservation assessment showing high priority for conservation according to the index. Finally, we provide recommendations for future collecting, research and management, to conserve banana and plantain crop wild relatives in seed banks for future generations ispartof: Food And Energy Security vol:11 issue:1 ispartof: location:England status: Published online

The ability of seeds to withstand drying is fundamental to ex situ seed conservation but drying responses are not well known for most wild species including crop wild relatives. We look at drying responses of seeds of Musa acuminata and Musa balbisiana, the two primary wild relatives of bananas and plantains, using the following four experimental approaches: (i) We equilibrated seeds to a range of relative humidity (RH) levels using non-saturated lithium chloride solutions and subsequently measured moisture content (MC) and viability. At each humidity level we tested viability using embryo rescue (ER), tetrazolium chloride staining and germination in an incubator. We found that seed viability was not reduced when seeds were dried to 4% equilibrium relative humidity (eRH; equating to 2.5% MC). (ii) We assessed viability of mature and less mature seeds using ER and germination in the soil and tested responses to drying. Findings showed that seeds must be fully mature to germinate and immature seeds had negligible viability. (iii) We dried seeds extracted from ripe/unripe fruit to 35-40% eRH at different rates and tested viability with germination tests in the soil. Seeds from unripe fruit lost viability when dried and especially when dried faster; seeds from ripe fruit only lost viability when fast dried. (iv) Finally, we dried and re-imbibed mature and less mature seeds and measured embryo shrinkage and volume change using X-ray computer tomography. Embryos of less mature seeds shrank significantly when dried to 15% eRH from 0.468 to 0.262 mm3, but embryos of mature seeds did not. Based on our results, mature seeds from ripe fruit are desiccation tolerant to moisture levels required for seed genebanking but embryos from immature seeds are mechanistically less able to withstand desiccation, especially when water potential gradients are high. ispartof: Conservation Physiology vol:10 issue:1 pages:1-16 ispartof: location:England status: Published online

Understanding the relative longevity of different seed lots, perhaps of different species or genotypes, but also following production under different environments or using different cultivation methods, or following different post-harvest treatments, is relevant to anyone concerned with the retention of seed lot viability and vigour during storage. However, different scientists over the years have used different conditions to assess seed lot longevity, as well as different variables as the measure of ‘longevity.’ Here, we give some of the backgrounds to how two standard protocols, with an open and closed system respectively, were derived, and explain why we considerp50, defined as the time during storage when seed lot viability, as measured through a germination test, has declined to 50%, is a suitable longevity trait parameter.

There is a pressing need to conserve plant diversity to prevent extinctions and to enable sustainable use of plant material by current and future generations. Here, we review the contribution that living collections and seed banks based in botanic gardens around the world make to wild plant conservation and to tackling global challenges. We focus in particular on the work of Botanic Gardens Conservation International and the Millennium Seed Bank of the Royal Botanic Gardens, Kew, with its associated global Partnership. The advantages and limitations of conservation of plant diversity as both living material and seed collections are reviewed, and the need for additional research and conservation measures, such as cryopreservation, to enable the long-term conservation of ‘exceptional species’ is discussed. We highlight the importance of networks and sharing access to data and plant material. The skill sets found within botanic gardens and seed banks complement each other and enable the development of integrated conservation (linking in situ and ex situ efforts). Using a number of case studies we demonstrate how botanic gardens and seed banks support integrated conservation and research for agriculture and food security, restoration and reforestation, as well as supporting local livelihoods.

1. Ecologically meaningful seed germination experiments are constrained by access to seeds and relevant environments for testing at the same time. This is particularly the case when research is carried out far from the native area of the studied species. 2. Here, we demonstrate an alternative - the use of glass houses in botanic gardens as simulated-natural habitats to extend the ecological interpretation of germination studies. Our focal taxa were banana crop wild relatives (Musa acuminata subsp. burmannica, M. acuminata subsp. siamea and M. balbisiana), native to tropical and subtropical Southeast Asia. Tests were carried out in Belgium, where we performed germination tests in relation to exposure to sun and foliage-shading, seed burial-depth in different heated glass house compartments, as well as seed survival and dormancy release in the soil. We anchored the interpretation of these studies by also conducting an experiment in a semi-natural habitat in the species native range (M. balbisiana - Los Baños, the Philippines), where we tested germination responses to exposure to the sun and shade. Using temperature data loggers, we determined temperature dynamics suitable for germination in both these settings. 3. In semi-natural and simulated-natural habitats, seeds germinated in response to exposure to direct solar radiation. Seed burial-depth had a significant but marginal effect by comparison, even when seeds were buried to 7cm in the soil. Temperatures at sun-exposed compared to shaded environments differed by only a few degrees Celsius. Maximum temperature of the period prior to germination was the most significant contributor to germination responses and germination increased linearly above a threshold of 23°C to the maximum temperature in the soil (in simulated natural habitats) of 35°C. 4. Glass houses can provide useful environments to aid interpretation of seed germination responses to environmental niches.

At the time of writing, in the UK and Northwest Europe the wood anemone (Anemone nemorosa L., Ranunculaceae) is in full flower, as Spring gets under way. This common herbaceous perennial of woodland and hedgerows is a possibly somewhat extreme example of the challenges facing conservationists striving to preserve seeds of their native species, in all their diversity, ex situ in conventional seed banks. Its seeds will survive drying, but only after the achenes, still green when shed, are dispersed from the parent plant. Ali et al. (2007) observed an initial increase in desiccation tolerance, followed by a decline; and the proportion of seeds surviving desiccation and their increase in subsequent longevity coincided with the growth and development of their embryos ex planta. However, developmental arrest of the embryo was not required for the acquisition of desiccation tolerance, and continued growth and development of the embryo resulted in loss of desiccation tolerance, analogous to that seen in orthodox (sensu Roberts, 1973) seeds upon radicle emergence. Consequently, the window of desiccation tolerance and maximum potential longevity is comparatively short; and in nature occurs when seeds are on or close to the soil surface. Though the seeds can be air-dried with care and stored at sub-zero temperatures, high initial viabilities are difficult to achieve and their storage lives are short (ten years or less under conventional seed bank conditions); throwing doubt on the role of conventional seed banking as a means of long, or even medium-term ex situ conservation for this species. Furthermore, while A. nemorosa seeds, like those of many species from the Ranunculaceae, might be described as having morphological or morphophysiological dormancy (Baskin and Baskin, 2014), the observed lack of developmental arrest is somewhat at odds with most definitions of dormancy.

Seed banks were first established to conserve crop genetic diversity, but seed banking has more recently been extended to wild plants, particularly crop wild relatives (CWRs) (e.g., by the Millennium Seed Bank (MSB), Royal Botanic Gardens Kew). CWRs have been recognised as potential reservoirs of beneficial traits for our domesticated crops, and with mounting evidence of the importance of the microbiome to organismal health, it follows that the microbial communities of wild relatives could also be a valuable resource for crop resilience to environmental and pathogenic threats. Endophytic fungi reside asymptomatically inside all plant tissues and have been found to confer advantages to their plant host. Preserving the natural microbial diversity of plants could therefore represent an important secondary conservation role of seed banks. At the same time, species that are reported as endophytes may also be latent pathogens. We explored the potential of the MSB as an incidental fungal endophyte bank by assessing diversity of fungi inside stored seeds. Using banana CWRs in the genus Musa as a case-study, we sequenced an extended ITS-LSU fragment in order to delimit operational taxonomic units (OTUs) and used a similarity and phylogenetics approach for classification. Fungi were successfully detected inside just under one third of the seeds, with a few genera accounting for most of the OTUs–primarily Lasiodiplodia, Fusarium, and Aspergillus–while a large variety of rare OTUs from across the Ascomycota were isolated only once. Fusarium species were notably abundant–of significance in light of Fusarium wilt, a disease threatening global banana crops–and so were targeted for additional sequencing with the marker EF1α in order to delimit species and place them in a phylogeny of the genus. Endophyte community composition, diversity and abundance was significantly different across habitats, and we explored the relationship between community differences and seed germination/viability. Our results show that there is a previously neglected invisible fungal dimension to seed banking that could well have implications for the seed collection and storage procedures, and that collections such as the MSB are indeed a novel source of potentially useful fungal strains.

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.

Ex situ seed conservation of banana crop wild relatives (Musa spp. L.), is constrained by critical knowledge gaps in their storage and germination behaviour. Additionally, challenges in collecting seeds from wild populations impact the quality of seed collections. It is, therefore, crucial to evaluate the viability of seeds from such collecting missions in order to improve the value of future seed collections. We evaluate the seed viability of 37 accessions of seven Musa species, collected from wild populations in Papua New Guinea, during two collecting missions. Seeds from one mission had already been stored in conventional storage (dried for four months at 15% relative humidity, 20 &deg, C and stored for two months at 15% relative humdity, &minus, 20 &deg, C), so a post-storage test was carried out. Seeds from the second mission were assessed freshly extracted and following desiccation. We used embryo rescue techniques to overcome the barrier of germinating in vivo Musa seeds. Seeds from the first mission had low viability (19 &plusmn, 27% mean and standard deviation) after storage for two months at 15% relative humidity and &minus, C. Musa balbisiana Colla seeds had significantly higher post-storage germination than other species (p &lt, 0.01). Desiccation reduced germination of the seeds from the second collecting mission, from 84 &plusmn, 22% (at 16.7 &plusmn, 2.4% moisture content) to 36 &plusmn, 30% (at 2.4 &plusmn, 0.8% moisture content). There was considerable variation between and (to a lesser extent) within accessions, a proportion of individual seeds of all but one species (Musa ingens N.W.Simmonds) survived desiccation and sub-zero temperature storage. We identified that seeds from the basal end of the infructescence were less likely to be viable after storage (p &lt, 0.001), and made morphological observations that identify seeds and infructescences with higher viability in relation to their developmental maturity. We highlight the need for research into seed eco-physiology of crop wild relatives in order to improve future collecting missions.

Loss of sexual reproductive capacity has been proposed as a syndrome of domestication in vegetatively propagated crops, but there are relatively few examples from agricultural systems. In this study we compare sexual reproductive capacity in wild (sexual) and domesticated (vegetative) populations of enset (Ensete ventricosum (Welw.) Cheesman), a tropical banana relative and Ethiopian food security crop.We examined floral and seed morphology and germination ecology across 35 wild and domesticated enset. We surveyed variation in floral and seed traits, including seed weight, viability and internal morphology, and germinated seeds across a range of constant and alternating temperature regimes to characterise optimum germination requirements.We report highly consistent floral allometry, seed viability, internal morphology and days to germination in wild and domesticated enset. However, seeds from domesticated plants responded to cooler temperatures with greater diurnal range. Shifts in germination behaviour appear concordant with a climatic envelope shift in the domesticated distribution.Our findings provide evidence that sexual reproductive capacity has been maintained despite long-term near-exclusive vegetative propagation in domesticated enset. Furthermore, certain traits such as germination behaviour and floral morphology, may be under continued selection, presumably through rare sexually reproductive events. Compared to sexually propagated crops banked as seeds, vegetative crop diversity is typically conserved in living collections that are more costly and insecure. Improved understanding of sexual propagation in vegetative crops may have applications in germplasm conservation and plant breeding.

Seed movement and delayed germination have long been thought to represent alternative risk-spreading strategies, but current evidence covers limited scales and yields mixed results. Here we present the first global-scale test of a negative correlation between dispersal and dormancy. The result demonstrates a strong and consistent pattern that species with dormant seeds have reduced spatial dispersal, also in the context of life-history traits such as seed mass and plant lifespan. Long-lived species are more likely to have large, non-dormant seeds that are dispersed far. Our findings provide robust support for the theoretical prediction of a dispersal trade-off between space and time, implying that a joint consideration of risk-spreading strategies is imperative in studying plant life-history evolution. The bet-hedging patterns in the dispersal-dormancy correlation and the associated reproductive traits have implications for biodiversity conservation, via prediction of which plant groups would be most impacted in the changing era.

Background and aims Seed desiccation response plays an important role in plant regeneration ecology, and has significant implications for species conservation. The majority of seed plants produce desiccation-tolerant (orthodox) seeds, whilst comparatively few produce desiccation-sensitive (recalcitrant) seeds that are unable to survive dehydration, and which cannot be conserved in traditional seed banks. This study develops a set of models to predict seed desiccation response in unstudied species. Methods Taxonomy, trait, location and climate data were compiled to form a global data set of 17 539 species. Three boosted regression trees models were then developed to predict species' seed desiccation responses based on habitat and trait information for the species, and the seed desiccation responses of close relatives (either members of the same genus, family or order, depending on the model). Ten-fold cross-validation was used to test model predictive success. The utility of the models was then demonstrated by predicting seed desiccation response for two floras: Ecuador, and Britain and Ireland. Key results The three models had varying success rates for identifying the desiccation-sensitive species: 89 % for the genus-level model, 79 % for the family-level model and 60 % for the order-level model. The most important predictor variables were the seed desiccation responses of a species' relatives, seed mass and annual precipitation. It is predicted that 10 % of seed plants from Ecuador and 1.2 % of those from Britain and Ireland produce desiccation-sensitive seeds. Due to data availability, prediction accuracy is likely to be higher for the British and Irish flora, where it is estimated that a desiccation-sensitive species had a 96.7 % chance of being correctly identified, compared with 80.8 % in the Ecuador flora. Conclusions These models can utilize existing data to predict species' likely seed desiccation responses, providing a gap-filling tool for global studies of plant traits, as well as critical decision-making support for plant conservation activities.

Effective seed storage after sourcing (harvesting or purchasing) is critical to restoration practitioners and native seed producers, as it is key to maintaining seed viability. Inadequate seed storage can lead to a waste of both natural and economic resources when seeds of poor quality are sown. When working with native species with unknown storage behavior, general assumptions can be made based on studies on related species, and standard practices may be applied with caution; however, an investigation should be conducted to understand if specific storage requirements are needed and for how long seeds can be stored before they lose significant viability. In this paper of the Special Issue Standards for Native Seeds in Ecological Restoration, we provide an overview of the key concepts in seed storage and the steps to take for effective storage of native seeds for restoration use.

The Global Strategy for Plant Conservation requires 75% of threatened plant species conserved ex situ by 2020. Currently, ex situ conservation focuses on conventional seed banking, yet this method is unsuitable for many threatened species. The 75% target is unattainable without urgent investment into alternative techniques.

Summary 1.The ability of seeds to tolerate desiccation plays an important role in plant regeneration ecology. Globally, the majority of species produce desiccation-tolerant (orthodox) seeds, whilst comparatively few produce desiccation-sensitive (recalcitrant) seeds that are unable to survive dehydration. The trait has important implications for species conservation, as desiccation-sensitive species cannot be conserved using traditional seed banking techniques. Additionally, these species may be less resilient to the increases in droughts predicted for some regions under climate change scenarios. 2.The best available resource on seed desiccation tolerance is the Royal Botanic Gardens, Kew's Seed Information Database. This database contains seed desiccation sensitivity data for over 18 000 taxa, approximately 3% of which have desiccation-sensitive seeds. However, this database is likely biased towards desiccation-tolerant species. Previous attempts to estimate the proportion of seed plants with desiccation-sensitive seeds have ranged from 7% to 50%. Here, we aimed to overcome sampling bias to derive a best estimate for the proportion of seed plants with desiccation-sensitive seeds, based on current data. 3.We used a recently developed method, based on taxonomic relatedness, to account for sampling bias and estimate the proportion of seed plants with desiccation-sensitive seeds. As a comparison, given that seed desiccation-sensitivity is strongly related to habitat, we repeated our analyses using habitat as a basis. 4.The predictions from our taxonomy-based models ranged between estimates of 7.5 and 19.6% of the world's seed plant species with desiccation-sensitive seeds, depending on model type, whilst the habitat-based models suggested a value of approximately 8%. Our evidence suggests that, based on current data, the best estimate of the proportion of species with desiccation-sensitive seeds is likely to be approximately 8%. Tropical and subtropical moist broadleaf forests had the highest incidence of seed desiccation-sensitivity, where an estimated 18.5% of the seed plant flora possessed the trait. 5.Synthesis. Alongside our estimation of the numbers of species with desiccation-sensitive seeds, we provide data on taxa and habitats where this trait may be most prevalent. These findings can be used to support conservation planning, particularly with respect to providing decision support for in and ex situ conservation techniques. This article is protected by copyright. All rights reserved.

Trait-based approaches have improved our understanding of plant evolution, community assembly and ecosystem functioning. A major challenge for the upcoming decades is to understand the functions and evolution of early life-history traits, across levels of organization and ecological strategies. Although a variety of seed traits are critical for dispersal, persistence, germination timing and seedling establishment, only seed mass has been considered systematically. Here we suggest broadening the range of morphological, physiological and biochemical seed traits to add new understanding on plant niches, population dynamics and community assembly. The diversity of seed traits and functions provides an important challenge that will require international collaboration in three areas of research. First, we present a conceptual framework for a seed ecological spectrum that builds upon current understanding of plant niches. We then lay the foundation for a seed-trait functional network, the establishment of which will underpin and facilitate trait-based inferences. Finally, we anticipate novel insights and challenges associated with incorporating diverse seed traits into predictive evolutionary ecology, community ecology and applied ecology. If the community invests in standardized seed-trait collection and the implementation of rigorous databases, major strides can be made at this exciting frontier of functional ecology., Commonwealth Scientific and Industrial Research Organisation. Grant Number: R‐90470‐01

Aim Functional traits of organisms are key to understanding and predicting biodiversity and ecological change, which motivates continuous collection of traits and their integration into global databases. Such trait matrices are inherently sparse, severely limiting their usefulness for further analyses. On the other hand, traits are characterized by the phylogenetic trait signal, trait–trait correlations and environmental constraints, all of which provide information that could be used to statistically fill gaps. We propose the application of probabilistic models which, for the first time, utilize all three characteristics to fill gaps in trait databases and predict trait values at larger spatial scales. Innovation For this purpose we introduce BHPMF, a hierarchical Bayesian extension of probabilistic matrix factorization (PMF). PMF is a machine learning technique which exploits the correlation structure of sparse matrices to impute missing entries. BHPMF additionally utilizes the taxonomic hierarchy for trait prediction and provides uncertainty estimates for each imputation. In combination with multiple regression against environmental information, BHPMF allows for extrapolation from point measurements to larger spatial scales. We demonstrate the applicability of BHPMF in ecological contexts, using different plant functional trait datasets, also comparing results to taking the species mean and PMF. Main conclusions Sensitivity analyses validate the robustness and accuracy of BHPMF: our method captures the correlation structure of the trait matrix as well as the phylogenetic trait signal – also for extremely sparse trait matrices – and provides a robust measure of confidence in prediction accuracy for each missing entry. The combination of BHPMF with environmental constraints provides a promising concept to extrapolate traits beyond sampled regions, accounting for intraspecific trait variability. We conclude that BHPMF and its derivatives have a high potential to support future trait-based research in macroecology and functional biogeography.

Germination is the first essential stage in crop and food production, as well as for the establishment of trees and regeneration of wild species. Temperature and water potential are the primary environmental factors that control germination in all species, and affect both the rate and final percentage germination. A comprehensive description of intra- and inter-variations between groups of species (perennials and annuals, trees, grasses, crops and wild species) helps understand where these species are currently able to grow on earth and will be in the future. By collecting germination trait data on 243 species from the literature and unpublished data, we provide a wide spectrum of species' seed germination traits, in the form of a set of parameter values describing germination responses to variations in temperature and water potential. Major differences in germination traits were seen to depend on the climatic conditions where the species grow or originated, with species able to germinate on ice and others unable to germinate below 18 degrees C. By contrast, within the different plant groups, similar ranges of threshold values were found, linked to the species geo-climatic origin. Crops however germinate faster, their range of threshold temperatures and water potential values is wider, and some crops have higher optimum and maximum temperatures as well as lower water potential threshold values. This is likely the result of human selection for rapid germination and for species able to grow in the wide range of environmental conditions where agriculture was developed. Our analyses revealed correlation between traits: negative correlations appeared between germination speed and temperature thresholds, and between temperature and water potential thresholds. The collected data also form a valuable database, enabling plant establishment to be better taken into account in modeling and simulation studies of vegetation boundaries (wild or cultivated) under changing land-use and climate. (C) 2014 Elsevier B.V. All rights reserved.

Ex situ conservation efforts such as those of zoos, botanical gardens, and seed banks will form a vital complement to in situ conservation actions over the coming decades. It is therefore necessary to pay the same attention to the biological diversity represented in ex situ conservation facilities as is often paid to protected-area networks. Building the phylogenetic diversity of ex situ collections will strengthen our capacity to respond to biodiversity loss. Since 2000, the Millennium Seed Bank Partnership has banked seed from 14% of the world's plant species. We assessed the taxonomic, geographic, and phylogenetic diversity of the Millennium Seed Bank collection of legumes (Leguminosae). We compared the collection with all known legume genera, their known geographic range (at country and regional levels), and a genus-level phylogeny of the legume family constructed for this study. Over half the phylogenetic diversity of legumes at the genus level was represented in the Millennium Seed Bank. However, pragmatic prioritization of species of economic importance and endangerment has led to the banking of a less-than-optimal phylogenetic diversity and prioritization of range-restricted species risks an underdispersed collection. The current state of the phylogenetic diversity of legumes in the Millennium Seed Bank could be substantially improved through the strategic banking of relatively few additional taxa. Our method draws on tools that are widely applied to in situ conservation planning, and it can be used to evaluate and improve the phylogenetic diversity of ex situ collections.

Question: Are plant traits more closely correlated with mean annual temperature, orwithmean annual precipitation? Location: Global. Methods: We quantified the strength of the relationships between temperature and precipitation and 21 plant traits from 447,961 species-site combinations worldwide. We used meta-analysis to provide an overall answer to our question. Results: Mean annual temperature was significantly more strongly correlated with plant traits than was mean annual precipitation. Conclusions: Our study provides support for some of the assumptions of classical vegetation theory, and points to many interesting directions for future research. The relatively low R

The Millennium Ecosystem Assessment estimates that between 60,000 and 100,000 plant species are threatened with extinction–equivalent to around one-quarter of the total number of known plant species. Why should we care? There are a number of reasons. The first is that these plants may be useful to us in unknown ways. Secondly, ecology has taught us that resilience is found in diversity. Thirdly, we should be saving plant species from extinction because we can–there is no technological reason why any plant species should become extinct. Where we can't protect and manage plant diversity in situ, we should be employing ex situ conservation techniques, ranging from seed banks to habitat restoration. The Millennium Ecosystem Assessment describes such interventions as ‘techno-gardening’. This is not an abstract concept–it is already a reality in the majority of man-managed landscapes. In this context the perception of ex situ conservation as simply a back-up strategy for in situ conservation is mistaken. We are all involved in ex situ conservation to some degree, from cultivating our back gardens, to farming, to management of protected areas. Ex situ conservation should be seen as a complementary approach to in situ conservation and on the same spectrum. Kew's Millennium Seed Bank Partnership, comprising more than 120 plant science institutions in 50 countries, epitomizes this philosophy in action. We work actively on every seed collection we bank, finding out how useful it is and how we can grow it to enable human innovation, adaptation and resilience. Challenges remain at the policy level; for example, the need to factor-in the value of natural capital to development decision making, and better defining a role for public-sector science. At the technical level, also, there is much to do. Perhaps the greatest technical challenges relate to the restoration and management of complex, self-sustaining habitats or species assemblages. If we are to techno-garden effectively, in order to maintain ecosystem services and sustain biodiversity, then a multidisciplinary approach will be required. Many plant science institutions have recognized this and are becoming engaged increasingly in restoration activities and in situ management. Ultimately, humanity's ability to innovate and adapt is dependent on our having access to the full range of plant species and the alleles they contain.

Aim To provide the first global quantification of the slope and shape of the latitudinal gradient in seed mass, and to determine whether global patterns in seed mass are best explained by growth form, vegetation type, seed dispersal syndrome, or net primary productivity (NPP). Location Global. Methods We collected seed mass data for 11,481 species × site combinations from around the world. We used regression to describe the latitudinal gradient in seed mass, then applied general linear models to quantify the relative explanatory power of each of the variables hypothesized to underlie the latitudinal gradient in seed size. Results There is a 320-fold decline in geometric mean seed mass between the equator and 60°. This decline is not linear. At the edge of the tropics, there is a sudden 7-fold drop in mean seed mass. The strongest correlates of the latitudinal gradient in seed mass are plant growth form, and vegetation type, followed by dispersal syndrome and NPP. A model including growth form, vegetation type, dispersal syndrome and NPP explains 51% of the variation in seed mass. Latitude explains just 0.2% of the residual variation from this model. Main conclusions This is the first demonstration of a major decrease in seed size at the edge of the tropics. This drop in seed mass is most closely correlated with changes in plant growth form and vegetation type. This suggests that the drop in seed mass might be part of a sudden change in plant strategy at the edge of the tropics.

Earth is home to a remarkable diversity of plant forms and life histories, yet comparatively few essential trait combinationshave proved evolutionarily viable in today?s terrestrial biosphere. By analysing worldwide variation in six major traitscritical to growth, survival and reproduction within the largest sample of vascular plant species ever compiled, we foundthat occupancy of six-dimensional trait space is strongly concentrated, indicating coordination and trade-offs. Threequartersof trait variation is captured in a two-dimensional global spectrum of plant form and function. One majordimension within this plane reflects the size of whole plants and their parts; the other represents the leaf economicsspectrum, which balances leaf construction costs against growth potential. The global plant trait spectrum provides abackdrop for elucidating constraints on evolution, for functionally qualifying species and ecosystems, and for improvingmodels that predict future vegetation based on continuous variation in plant form and function. Fil: Díaz, Sandra Myrna. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina Fil: Kattge, Jens. Max Planck Institute for Biogeochemistry; Alemania Fil: Cornelissen, Johannes H. C.. Vrije Universiteit; Países Bajos Fil: Wright, Ian J.. Macquarie University; Australia Fil: Lavorel, Sandra. Université Grenoble Alpes; Francia Fil: Dray, Stéphane. Université Lyon; Francia Fil: Reu, Björn. University of Leipzig; Francia Fil: Kleyer, Michael. University of Oldenburg; Alemania Fil: Wirth, Christian. Max Planck Institute for Biogeochemistry; Alemania Fil: Prentice, I. Colin. Macquarie University; Australia Fil: Garnier, Eric. Université Paul-Valéry Montpellier; Francia Fil: Bönisch, Gerhard. Max Planck Institute for Biogeochemistry; Alemania Fil: Westoby, Mark. Macquarie University; Australia Fil: Poorter, Hendrik. Forschungszentrum Jülich GmbH; Alemania Fil: Reich, Peter B.. University of Minnesota; Estados Unidos. University of Western Sydney; Australia Fil: Moles, Angela T.. University of New South Wales; Australia Fil: Dickie, John. The Royal Botanic Gardens Kew; Reino Unido Fil: Gillison, Andrew N.. Center for Biodiversity Management; Australia Fil: Zanne, Amy E.. George Washington University; Estados Unidos. Missouri Botanical Garden; Estados Unidos Fil: Chave, Jérôme. Université Paul Sabatier; Francia Fil: Wright, S. Joseph. Smithsonian Tropical Research Institute; Estados Unidos Fil: Sheremetev, Serge N.. Komarov Botanical Institute; Rusia Fil: Jactel, Hervé. Université de Bordeaux; Francia Fil: Baraloto, Christopher. Florida International University; Estados Unidos. Ecologie des Forêts de Guyane; Guayana Francesa Fil: Cerabolini, Bruno. University of Insubria; Italia Fil: Pierce, Simon. University of Milan; Italia Fil: Shipley, Bill. Université de Sherbrooke; Canadá Fil: Kirkup, Donald. The Royal Botanic Gardens Kew; Reino Unido Fil: Casanoves, Fernando. Centro Agronómico Tropical de Investigación y Enseñanza; Costa Rica Fil: Joswig, Julia S.. Max Planck Institute for Biogeochemistry; Alemania Fil: Günther, Angela. Max Planck Institute for Biogeochemistry; Alemania Fil: Falczuk, Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina Fil: Rüger, Nadja. German Centre for Integrative Biodiversity Research; Alemania Fil: Mahecha, Miguel D.. Max Planck Institute for Biogeochemistry; Alemania Fil: Gorne, Lucas Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina

Improved phylogenies and the accumulation of broad comparative data sets have opened the way for phylogenetic analyses to trace trait evolution in major groups of organisms. We arrayed seed mass data for 12,987 species on the seed plant phylogeny and show the history of seed size from the emergence of the angiosperms through to the present day. The largest single contributor to the present-day spread of seed mass was the divergence between angiosperms and gymnosperms, whereas the widest divergence was between Celastraceae and Parnassiaceae. Wide divergences in seed size were more often associated with divergences in growth form than with divergences in dispersal syndrome or latitude. Cross-species studies and evolutionary theory are consistent with this evidence that growth form and seed size evolve in a coordinated manner.

Summary 1 The ability of seeds to survive desiccation is an important functional trait and is an integral part of plant regeneration ecology. Despite this, the topic has received relatively little attention from ecologists. In this study, we examine the relationships between seed desiccation tolerance and two important aspects of plant regeneration ecology: habitat and dormancy. This is done by comparative analysis of a data set of 886 tree and shrub species from 93 families. 2 The proportion of species displaying desiccation sensitive seeds declines as the habitat becomes drier, and possibly also cooler, although the latter observation requires cautious interpretation. Desiccation sensitivity is most common in moist, relatively aseasonal vegetation zones, but is infrequent in, though not absent from arid and highly seasonal habitats. 3 The highest frequency of desiccation sensitivity occurs in non-pioneer evergreen rain forest trees, although 48% of the species examined have desiccation tolerant seeds. In contrast, all pioneer taxa within the data set have drying tolerant seeds. 4 Desiccation sensitivity is more frequent in seeds that are non-dormant on shedding ( c. 31%), than dormant ( c. 9%). Highest frequencies of drying tolerance occur in seeds with physical or combinational dormancy, at 99% and 100%, respectively. 5 Although there is an association between non-dormancy and desiccation sensitivity in both tropical and temperate zones, the relationship does not appear to be causal. 6 Wo rking from the hypothesis that seed desiccation sensitivity represents a derived state in extant species, we use the results to investigate and discuss possible ecological trade-offs and associated fitness advantages. These may explain the hypothesized repeated loss of this trait. The frequent association between large seed size and desiccation sensitivity is also considered.

The Royal Botanic Gardens Kew manages the Millennium Seed Bank (MSB) Partnership, the largest ex situ conservation program for wild plant species in the world. The long-term storage of viable dry seed collections ('orthodox' seeds) in deep-freeze chambers and maintaining their quality, viability and longevity for future use are central to the conservation effort. Seed collections conserved within the vault of MSB represent the highest concentration of living seed-plant biodiversity on earth with over 83,500 collections from 37,940 vascular plant species originating from nine bio-geographical areas, 189 countries and territories, 35 biodiversity hotspots, 357 families and 5821 genera. Curation of living seeds from such diversity and wide geographic origin is challenging and requires breadth and depth of knowledge, resources and experience in taxonomy and seed biology, physiology, morphology and ecology in order to understand taxon level seed traits related to seed viability, germination and survival in long-term storage. We describe how biodiversity informatics are integrated with collection and trait data to develop decision and prediction tools to support curators and collection professionals at MSB to address challenges in decision making during curatorial activities to best allocate their conservation effort. Bringing these disciplines together and bridging the gaps require accurate data acquisition, sharing, analysis and interoperability. MSB met these challenges through collaboration and establishing and sharing data standards, structures, algorithms and resources with MSB Partnership, currently across 95 countries. A range of databases and tools are central to carrying out the daily routine work of curators at MSB. (1) The Seed Bank Database (SBD) captures collection level data from the point of sampling and throughout their lifespan in storage. It is the main data hub used to manage collections. SBD includes mathematical and statistical computations to monitor quality, quantity and viability of collections. (2) The Taxon Database (TDB) consolidates the plant name backbone with taxonomic identities of collections. It enables curators to identify the taxon to allocate the correct curation protocol for conservation. (3) The Seed Information Database (SID) serves as a main source of a variety of taxon-based biological information for use in large scale analysis and decision support. It is a compilation of seed biological trait data (weights, storage behavior, germination, viability constant, protein content, oil content, morphology, dispersal) from MSB Partnership collections and other published and unpublished sources. SID, which is in public domain (http://data.kew.org/sid/), also provides useful tools that incorporate mathematical models to predict viability of seeds after period of storage in range of environments. SID data are used at MSB to predict seed storage behavior and to identify short-lived taxa in long-term storage. (4) The Data Analysis and Reporting Tool (DART) serves as the user interface where SBD, TDB, SID and other Kew databases can be linked. It is the main tool used for data querying, analysis, and visualization. (5) The Germination Predictor Tool uses MSB Collection data (month of seed dispersal, geo-coordinates and seed germination) and world climatic data (precipitation and temperature) to predict conditions and treatments that are required to germinate seeds based on taxonomy and geographic origin of collections. This enables curators to simulate conditions that trigger germination of seeds in their natural environment. Kew's UK Germination toolbox, which is in the public domain (http://data.kew.org/ukgerm/search), mostly uses SBD germination data and provides successful germination conditions for UK native species. (6) The Species Prioritization Tool ranks vascular plant taxa by using an integrative assessment technique that incorporates taxon level data compiled from several Kew and open databases to yield priority scores based on multiple priority-setting criteria. It is used by collection managers during collection acquisition and management to identify conservation priority taxa and collections. The above examples of applications used at the MSB show clearly how biodiversity data provides essential systems for collection management in ex situ conservation.

Ex situ conservation efforts such as those of zoos, botanical gardens, and seed banks will form a vital complement to in situ conservation actions over the coming decades. It is therefore necessary to pay the same attention to the biological diversity represented in ex situ conservation facilities as is often paid to protected-area networks. Building the phylogenetic diversity of ex situ collections will strengthen our capacity to respond to biodiversity loss. Since 2000, the Millennium Seed Bank Partnership has banked seed from 14% of the world's plant species. We assessed the taxonomic, geographic, and phylogenetic diversity of the Millennium Seed Bank collection of legumes (Leguminosae). We compared the collection with all known legume genera, their known geographic range (at country and regional levels), and a genus-level phylogeny of the legume family constructed for this study. Over half the phylogenetic diversity of legumes at the genus level was represented in the Millennium Seed Bank. However, pragmatic prioritization of species of economic importance and endangerment has led to the banking of a less-than-optimal phylogenetic diversity and prioritization of range-restricted species risks an underdispersed collection. The current state of the phylogenetic diversity of legumes in the Millennium Seed Bank could be substantially improved through the strategic banking of relatively few additional taxa. Our method draws on tools that are widely applied to in situ conservation planning, and it can be used to evaluate and improve the phylogenetic diversity of ex situ collections.

n/a

The adaptation of plant species to their biotic and abiotic environment is manifested in their traits. Suites of correlated functional traits may reflect fundamental tradeoffs and general plant strategies and hence represent trait spectra along which plant species can vary according to their respective strategies. However, the functional interpretation of these trait spectra requires the inspection of their relation to plant performance. We employed principle coordinate analysis (PCoA) to quantify fundamental whole-plant trait spectra based on 23 traits for 305 North American woody species that span boreal to subtropical climates. We related the major axes of PCoA to five measures of plant performance (i.e., growth rate, and tolerance to drought, shade, water-logging and fire) for all species and separately for gymnosperms and angiosperms. Across all species a unified gymnosperm-angiosperm trait spectrum (wood density, seed mass, rooting habit) is identified, which is correlated with drought tolerance. Apart from this, leaf type and specific leaf area (SLA) strongly separate gymnosperms from angiosperms. For gymnosperms, one trait spectrum emerges (seed mass, rooting habit), which is positively correlated with drought tolerance and inversely with shade tolerance, reflecting a tradeoff between these two strategies due to opposing trait characteristics. Angiosperms are functionally more diverse. The trait spectra related to drought tolerance and shade tolerance are decoupled and three distinct strategies emerge: high drought tolerance (low SLA, dense wood, heavy seeds, taproot), high shade tolerance (high SLA, shallow roots, high toxicity, opposite arranged leaves), and fast growth/stress intolerance (large maximum heights, soft wood, light seeds, high seed spread rate). In summary, our approach reveals that complex suits of traits and potential tradeoffs underlie fundamental performance strategies in forests. Studies relying on small sets of plant traits may not be able to reveal such underlying strategies. Read More: http://www.esajournals.org/doi/abs/10.1890/ES13-00143.1

Given the widespread belief that the conservation of palms, especially the large-trunked species, is only accomplished throughin situ preservation or in plantations, this paper explores the feasibility of a third approach, i.e. cryogenic preservation of their seedsex situ. Seeds of the following palm species were subjected to air-drying to assess their tolerance of dessication:Washingtonia filifera (L. Linden) H. Wendl.;Sabal mexicana Mart. (syn. S. texana; Zong, 1990);Schippia concolor Burret;Orbignya cohune (Mart.) Dahlgren ex Standley;Acoelorraphe wrightii (Griseb. & H. Wendl.) H. Wendl. ex Becc.;Desmoncus orthacanthos Mart.;Attalea crassispatha (Mart.) Burret;Zambia antillarum (Desc.) L.H. Bailey;Pinanga malaiana (Mart.) Scheff.;Pinanga aff. polymorpha Becc.;Daemonorops verticillaris (Griff.) Mart. Of these, only two (W. filifera andS. mexicana) survived drying to moisture contents around 5% (fresh weight basis). Seeds of the remaining spp. would be difficult or impossible to conserveex situ in seedbanks or cryostores. Data are presented to show that the response ofO. cohune embryos to drying is similar to other recalcitrant (dessication intolerant) seeds, while seeds ofA. wrightii may belong to an intermediate seed storage category with limited tolerance of drying. The results are discussed in relation to the inadequacy of current knowledge as a basis for decisions on the broad scaleex situ conservation of palm germplasm.

Mature seeds of Norway maple (Acer platanoides L.) are tolerant of desiccation, at least to moisture contents of about 7% (fresh weight basis), but those of sycamore (Acer pseudoplatanus) are killed by drying below about 45% moisture content. Sycamore seeds are thus recalcitrant; while the classification of those of Norway maple as orthodox is confirmed by the fact that between 19% and 7.5% moisture content their longevity is increased in a predictable way by reduction of seed moisturecontent. However, the period of useful storage of the latter in seed banks may be much less than for many crop species. The rates of water loss to a dry environment of both fruits and seeds of sycamore are much less than those of Norway maple, suggesting a degree of desiccationavoidance in the desiccation-intolerant species. Seed physiological maturity (maximum dry weight) occurred 2–3 weeks earlier in Norway maple than insycamore, but in both species this occurred about 150–160 days after peak flowering. Tetrazolium staining is a good indicator of embryo viability in both species, correlating well with germination test results. In Norway maple both methods of viability testing indicated that whole-seed desiccation tolerance coincided with the attainment of maximum dry weight. Tetrazolium staining indicated the development of desiccation tolerance in the radicles/hypocotyls of both species approximately 2–4 weeks before physiological maturity. Possible correlation between changes in the level of embryo dormancy during development and the acquisition of desiccation tolerance are discussed.

Seed survival data for eight diverse species, namely the cereal barley (Hordeum vulgare L.), the grain legumes chickpea (Cicer arietinum L.), cowpea [Vigna unguiculata (L.) Walp.] and soya bean [Glycine max (L.) Merr.], the timber trees elm (Ulmus carpinifolia Gleditsch.), mahogany (Swietenia humilis Zucc.), and terb (Terminalia brassii Exell.), and the leaf vegetable lettuce (Lactuca saliva L.) were compared over a wide range of storage environments (temperatures from —13 °C to 90 °C, seed moisture contents from 1-8 to 25 % f.wt) using a viability equation developed previously. In accordance with that equation, the effect of temperature on seed longevity was dependent upon the temperature range. The temperature coefficients of the viability equation did not differ significantly (P > 005) among the eight species despite their contrasting taxonomy. Thus the quantitative relation between seed longevity and temperature does not vary among diverse species. The same conclusion was obtained for the coefficients of a proposed alternative model of the relation between seed longevity and temperature. The implications of the two temperature models in the viability equation for extrapolations to low and very low temperatures are discussed.

Summary • Previous investigators have identified strong positive relationships between genome size and seed mass within species, and across species from the same genus and family. • Here, we make the first broad-scale quantification of this relationship, using data for 1222 species, from 139 families and 48 orders. We analyzed the relationship between genome size and seed mass using a statistical framework that included four different tests. • A quadratic relationship between genome size and seed mass appeared to be driven by the large genome/seed mass gymnosperms and the many small genome size/large seed mass angiosperms. Very small seeds were never associated with very large genomes, possibly indicating a developmental constraint. Independent contrast results showed that divergences in genome size were positively correlated with divergences in seed mass. • Divergences in seed mass have been more closely correlated with divergences in genome size than with divergences in other morphological and ecological variables. Plant growth form is the only variable examined thus far that explains a greater proportion of variation in seed mass than does genome size.

We used correlated divergence analysis to determine which factors have been most closely associated with changes in seed mass during seed plant evolution. We found that divergences in seed mass have been more consistently associated with divergences in growth form than with divergences in any other variable. This finding is consistent with the strong relationship between seed mass and growth form across present-day species and with the available data from the paleobotanical literature. Divergences in seed mass have also been associated with divergences in latitude, net primary productivity, temperature, precipitation, and leaf area index. However, these environmental variables had much less explanatory power than did plant traits such as seed dispersal syndrome and plant growth form.

Mitotic metaphase chromosomes were counted in 29 taxa, representing 11 subgenera of Austrostipa, and in 11 species from nine related genera of the grass subfamily Pooideae. Karyotype features were also measured. The cytogenetic data were mapped on molecular phylogenetic trees based on nuclear ITS and plastid 3ʹtrnK DNA sequence data. The trees showed four different main lineages within Austrostipa, but supported only two of the 13 acknowledged subgenera. The phylogenetic positions of the genera Anemanthele, Achnatherum, Nassella and Oloptum indicated paraphyly of the genus Austrostipa. In nuclear-sequence data, Anemanthele was nested within Austrostipa; however, in plastid-sequence data, both were sisters. The newly obtained chromosome counts in Austrostipa showed that most species have 2n = 44, the other 2n = 66. Presuming a chromosome base number of x = 11, the counts corresponded with ploidy levels of 4x and 6x respectively. Karyotype data of Austrostipa and Anemanthele were very similar. Chromosome counting in further genera suggested chromosome base numbers of x = 9, 10, 11, 12 and 13. Chromosome sizes of the phylogenetically derived tribe Stipeae were smaller than those of the earliest diverging Pooideae lineages Nardeae, Meliceae and Phaenospermateae. The mechanisms of chromosome evolution and the origin of the considerable variation in chromosome base numbers in the subfamily Pooideae are discussed in the context of chromosome evolution and biosystematics.

Grubb et al . ([ 1 ][1]) suggest that the shape of the relation between seed mass and plant size is better explained by the mechanical-constraints hypothesis than by a coordination of life-history traits, as suggested by Moles et al . ([ 2 ][2]). Their preference for the mechanical-constraints idea