Grass seeds play a critical and fundamental role in grass breeding and production. Elymus sibiricus L. is a widespread Poaceae forage grass in northern Eurasia which is used for ecological restoration and forage production. Sucrose is the main source of substrate and energy required for starch synthesis in the seeds, so the hydrolysis of sucrose determines and influences starch synthesis and filling in the seeds, especially Poaceae. However, the process behind carbohydrate metabolism during E. sibiricus seed development remains unclear. This study addresses a significant gap in our understanding of the carbohydrate metabolism during seed development in E. sibiricus by employing full-length transcriptome sequencing across five developmental stages for the first time. Full-length transcriptome sequencing was performed on E. sibiricus seeds at five developmental stages (S5, S9, S15, S20, S25) to get better molecular insights. We identified 13,205 differentially expressed genes, with 7,471 up-regulated and 5,734 down-regulated. Through KEGG enrichment analysis, genes were enriched in ‘starch and sucrose metabolism’, ‘photosynthetic-related’ and ‘hormone signal transduction’ pathways. Gene ontology enrichment analysis showed that genes were enriched in the ‘beta-amylase activity’ term of molecular functions. In addition, top 21 transcription factor families were identified as involved in seed development. The homologous genes of ABSCISIC ACID-INSENSITIVE 3 (ABI3), NUCLEAR FACTOR-YB1 (NF-YB1), STARCH SYNTHASE I (SSI) were identified as candidate genes of seed development in E. sibiricus. Combined with physiological index, transcriptome analyses, weighted gene co-expression network analysis and real-time quantitative PCR, the mechanism of starch and sucrose content of seed development was revealed and ten hub genes were identified. Overall, this study provides the molecular bases to understand seed development and starch and sucrose metabolism at the different seed developmental stages in E. sibiricus.

To maximize seed longevity, seeds should be harvested at optimal maturity, that is, when seeds have acquired maximum physiological quality before deterioration begins. The aim of this study was to map the variation in temporal patterns of lentil (Lens culinaris Medik.) seed quality development when grown across four regeneration environments, which differ in the level of temperature and humidity control throughout the growing season, at the Australian Grains Genebank. Seeds of two lentil accessions (76080 and 76072) were harvested at different stages throughout development, commencing at 21 d after 50% anthesis until a maximum of 130 d. At each harvest, physiological quality traits, including germinability (fresh and dried seeds) and seed longevity, were determined, as well as seed dry weight and moisture content. Seeds of both accessions, and in all environments, started to accumulate physiological quality early on in development but did not reach their maximum until 3–54 d after mass maturity. The temporal patterns of desiccation tolerance and storage longevity were highly influenced by the environmental conditions during the maturation drying phase, affecting both ‘when’ maximum quality was attained and for how long it was maintained, thereafter. Seeds did not show a typical developmental response, rather variation was observed in seed quality development both between and within accessions grown in the different environments. The poorest storage longevity was seen when seeds of both accessions were grown in the cooler, temperature-controlled glasshouse, and the maximum longevity was observed in the warmer, semi-protected environments of the green and the big igloo for accessions 76080 and 76072, respectively.

The J. Derek Bewley Career Lectures presented at the triennial meetings of the International Society of Seed Science support early-career seed scientists by providing retrospective views, from those late in their careers, of lessons learned and future implications. Ambition, ability, inspiration, foresight, hard work and opportunity are obvious career requirements. The importance of mentoring and teamwork combined with the clear communication of results, understanding and ideas are emphasized. The role of illustration in research, and its dissemination, is outlined: illustration can support hypothesis development, testing and communication. Climate change may perturb the production of high-quality seed affecting conservation as well as agriculture, horticulture and forestry. An illustrative synthesis of the current understanding of temporal aspects of the effects of seed production environment on seed quality (assessed by subsequent seed storage longevity) is provided for wheat (Triticum aestivum L.) and rice (Oryza sativa L.). Seed science research can contribute to complex global challenges such as future food supplies from seed-propagated crops in our changing climate whilst conserving biological diversity (through seed ecology and technologies such as ex situ plant genetic resources conservation by long-term seed storage in genebanks), but only if that research can be – and then is – applied.

Flavonoids are a group of phenolic secondary metabolites in plants that have important physiological, ecological and economic value. In this study, using the desert plant Artemisia sphaerocephala Krasch. as the sample material, the content and components of the total flavonoids in its seeds at seven different developmental stages were determined. In addition, the genes involved in flavonoid metabolism were identified by full-length transcriptome sequencing (third-generation sequencing technology based on PacBio RS II). Their expression levels were analysed by RNA-seq short reading sequencing, to reveal the patterns and regulation mechanisms of flavonoid accumulation during seed development. The key results were as follows: the content of total flavonoids in mature seeds was 15.05 mg g−1, including five subclasses: flavonols, chalcones, flavones, flavanones and proanthocyanidins, among which flavonols accounted for 45.78%. The period of rapid accumulation of flavonoids was 40–70 d following anthesis. The high expression of phenylalanine ammonia-lyase (PAL), 4-coumarate-CoA ligase (4CL) and UDP-glucose:flavonoids 3-o-glucosyltransferase (UF3GT) promoted the accumulation of total flavonoids, while the high expression of flavonoids 3′-hydroxylase (F3′H) and flavonols synthase (FLS) made flavanols the main component. Transcription factors such as the MYB-bHLH-WDR (MBW) complex and Selenium-binding protein (SBP) directly regulated the structural genes of flavonoid metabolism, while C2H2-type zinc finger (C2H2), Zinc-finger transcription factor (GATA), Dehydration-responsive element binding (DREB), Global Transcription factor Group E protein (GTE), Trihelix DNA-binding factors (Trihelix) and Phytochrome-interacting factor (PIF) indirectly promoted the synthesis of flavonoids through hormones such as brassinoidsteroids (BRs) and abscisic acid (ABA). These results provided valuable resources for the application of related genes in genetics and breeding.

Common teasel is a troublesome invasive weed in North and South America. Additional information on the efficacy of herbicide application and mowing at different growth stages will help in common teasel management. First, an outdoor pot experiment was performed to assess the effects of increasing application rates and combinations of glyphosate and 2,4-D amine when applied at the 4-leaf, rosette, and bolting stages. Second, field experiments were performed to evaluate the impact of time of cutting on invasive common teasel height, head number, and head length. Finally, germinability of seeds collected from naturally growing plants was determined to evaluate the feasibility of mowing invasive common teasel after flowering. Only glyphosate applied at 1.08 kg ae ha−1 at the 4-leaf stage provided adequate control (>90%). Although control was not satisfactory (<90%) when applying glyphosate at 2.16 kg ae ha−1 at the rosette and bolting stages, and 2,4-D at 1.75 kg ai ha−1 at 4-leaf stage, significant injury and biomass decline were observed. Glyphosate and 2,4-D combinations did not improve common teasel control compared with single applications of each. Cutting rosettes strongly reduced inflorescence production (34%–49%) and cutting flowering plants prevented total regrowth. Germination of seeds averaged 14% when harvested 10 d after flowering, and maximum seed germination (>90%) occurred 30 d after flowering. Glyphosate applied alone at the recommended commercial rate early in the growing season, together with cutting at the flowering stage, may be the most beneficial way of controlling invasive common teasel.

Drought and high temperature each damage rice (Oryza sativa L.) crops. Their effect during seed development and maturation on subsequent seed quality development was investigated in Japonica (cv. Gleva) and Indica (cv. Aeron 1) plants grown in controlled environments subjected to drought (irrigation ended) and/or brief high temperature (HT; 3 days at 40/30°C). Ending irrigation early in cv. Gleva (7 or 14 days after anthesis, DAA) resulted in earlier plant senescence, more rapid decline in seed moisture content, more rapid seed quality development initially, but substantial decline later in planta in the ability of seeds to germinate normally. Subsequent seed storage longevity amongst later harvests was greatest with no drought because with drought it declined from 16 or 22 DAA onwards in planta, 9 or 8 days after irrigation ended, respectively. Later drought (14 or 28 DAA) also reduced seed longevity at harvest maturity (42 DAA). Well-irrigated plants provided poorer longevity the earlier during seed development they were exposed to HT (greatest at anthesis and histodifferentiation; no effect during seed maturation). Combining drought and HT damaged seed quality more than each stress alone, and more so in the Japonica cv. Gleva than the Indica cv. Aeron 1. Overall, the earlier plant drought occurred the greater the damage to subsequent seed quality; seed quality was most vulnerable to damage from plant drought and HT at anthesis and histodifferentiation; and seed quality of the Indica rice was more resilient to damage from these stresses than the Japonica.

The long-standing hypothesis that seed quality improves during seed filling, is greatest at the end of seed filling, and declines thereafter (because seed deterioration was assumed to begin then), provided a template for research in seed quality development. It was rejected by investigations where seed quality was shown to improve throughout both seed development and maturation until harvest maturity, before seed deterioration was first observed. Several other temporal patterns of seed quality development and decline have also been reported. These are portrayed and compared. The assessment suggests that the original hypothesis was too simple, because it combined several component hypotheses: (a) the seed improvement (only) phase ends before seed deterioration (only) commences; (b) there is only a brief single point in time during seed development and maturation when, in all circumstances, seed quality is maximal; (c) the seed quality improvement phase coincides perfectly with seed filling, with deterioration only post-seed filling. It is concluded that the search for the single point of maximum seed quality was a false quest because (a) seed improvement and deterioration may cycle (sequentially if not simultaneously) during seed development and maturation; (b) the relative sensitivity of the rates of improvement and deterioration to environment may differ; (c) the period of maximum quality may be brief or extended. Hence, when maximum quality is first attained, and for how long it is maintained, during seed development and maturation varies with genotype and environment. This is pertinent to quality seed production in current and future climates as it will be affected by climate change and a likelihood of more frequent coincidence of brief periods of extreme temperatures with highly sensitive phases of seed development and maturation. This is a possible tipping point for food security and for ecological diversity.

Multispectral imaging is a new technology that is being deployed to assess seed quality parameters. Examples of applications in the detection and identification of fungi on seeds are presented, together with an example of the technology used for maturity determination in sugar beet seed. Results from multispectral imaging are compared with reference methods, and a high correlation is found. Applications of the technique for varietal discrimination and insect damage are also presented. There is a need for non-destructive, reliable and fast techniques, and it is concluded that multispectral imaging has potential for seed quality assessment, in particular for those components associated with surface structure and chemical composition, seed colour, morphology and size.

The objective of this study was to evaluate the effect of day length after flowering on pollen tube elongation, embryo formation and seed development. The quinoa varieties used in this study were Amarilla de Marangani (valley type) and NL-6 (sea-level type). After sowing, the quinoa plants were cultivated in growth cabinets. From sowing to flowering, plants were exposed to a 15 h day length regime. After flowering, the plants were grown under either a 15 h or 11 h day length regime. The elongation of the pollen tube and the formation of the early embryo were not inhibited in either Amarilla de Marangani or NL-6 under the 11 or 15 h day length regimes. Although growth of the embryo in NL-6 was not inhibited by the 15 h day length regime after flowering, the same was not observed in the case for Amarilla de Marangani. In Amarilla de Marangani, seed diameter at 8 and 14 days after flowering under the 11 h day length regime was larger than that of seeds grown under the 15 h day length regime. Thus, the decrease in the number of seeds in Amarilla de Marangani grown under the 15 h day length regime may be caused by the suspension of embryo growth after fertilization.

Ethyl ester of DPX-Y6202 {2-[4-[(6-chloro-2-quinoxalinyl)oxy] phenoxy] propanoic acid} and butyl ester of fluazifop {(±)-2-[4-[[5-(trifluoromethyl)-2-pyridinyl] oxy] phenoxy] propanoic acid} applied during the reproductive phase of development at 0.07 and 0.28 kg ai/ha prevented seed formation in downy brome (Bromus tectorum L. # BROTE). Fluazifop prevented seed formation over a wider range of application rates and growth stages than did DPX-Y6202. Seed production was prevented most readily by herbicide applications made early in the reproductive phase. Environmental factors during reproduction affected herbicide performance. Foliar absorption and translocation of 14C-fluazifop into the developing spikelets was greater than that of 14C-DPX-Y6202 in downy brome.

Downy brome seed production was measured in the field following the establishment of different moisture levels using a line source sprinkler irrigation system. Results indicated that seed production was strongly affected by different moisture levels, with a curvilinear decrease in seed number from higher to lower moisture. In a hydroponic study with water deficits induced by PEG-8000, no seeds were produced when plants were severely stressed (-1.1 MPa) for a 7-day period during culm elongation or anthesis. Number of seeds/panicle was reduced under severe water stress during seed fill, under moderate stress (-0.5 MPa) during anthesis or seed fill, and under mild stress (-0.1 MPa) during anthesis. Water stress also reduced apparent photosynthesis and increased diffusive resistance of flag leaves, particularly under severe stress. In general, water deficits did not affect seed weights or germination percentages in either study.

A culture medium and environmental conditions were selected for ovule culture of velvetleaf (Abutilon theophrasti Medic. ♯4 ABUTH), which allowed development parallel to that occurring in vivo. Of the six nutrient media evaluated, the most suitable one contained an organic nitrogen source and was of high osmotic potential. A liquid medium with a pH of 5 to 7, and culture for 14 days at 25 C under green light (1.3 μmole·m-2·-1) encouraged good embryo and ovule development. No difference was recorded between polyethylene glycol 20000 and mannitol in the medium used for dehydration and subsequent imbibition of cultured mature ovules. To investigate the effects of maternal tissues, surgical alterations were performed on the testa and funiculus of immature velvetleaf ovules. The intact testa appears to be a barrier to nutrient absorption and reduces the fresh and dry weights and embryo length. Ovule and embryo development was significantly better if either the testa was nicked or the funiculus removed.

Integrated weed management (IWM) for agronomic and vegetable production systems utilizes all available options to effectively manage weeds. Late-season weed control measures are often needed to improve crop harvest and stop additions to the weed seed bank. Eliminating the production of viable weed seeds is one of the key IWM practices. The objective of this research was to determine how termination method and timing influence viable weed seed production of late-season weed infestations. Research was conducted in Delaware, Michigan, and New York over a 2-yr period. The weeds studied included: common lambsquarters, common ragweed, giant foxtail, jimsonweed, and velvetleaf. Three termination methods were imposed: cutting at the plant base (simulating hand hoeing), chopping (simulating mowing), and applying glyphosate. The three termination timings were flowering, immature seeds present, and mature seeds present. Following termination, plants were stored in the field in mesh bags until mid-Fall when seeds were counted and tested for viability. Termination timing influenced viable seed development; however, termination method did not. Common ragweed and giant foxtail produced viable seeds when terminated at the time of flowering. All species produced some viable seed when immature seeds were present at the time of termination. The time of viable seed formation varied based on species and site-year, ranging from plants terminated the day of flowering to 1,337 growing degree d after flowering (base 10, 0 to 57 calendar d). Viable seed production was reduced by 64 to 100% when common lambsquarters, giant foxtail, jimsonweed, and velvetleaf were terminated with immature seeds present, compared to when plants were terminated with some mature seeds present. Our results suggest that terminating common lambsquarters, common ragweed, and giant foxtail prior to flowering, and velvetleaf and jimsonweed less than 2 and 3 wk after flowering, respectively, greatly reduces weed seed bank inputs.

Downy brome in dryland winter wheat presents a major constraint to the adoption of reduced tillage cropping systems in the Pacific Northwest of the United States. Effective suppression of downy brome during fallow periods depletes seed in the soil and reduces infestations in subsequent winter wheat crops. Delayed tillage operations or delayed herbicide applications in the spring increase the risk for production of viable downy brome seed during fallow periods. In a series of studies, downy brome panicles were sequentially sampled at Pendleton, OR, and Pullman, WA, in 1996 and 1997, and at nine locations around the winter wheat growing region of the western United States in 1999 and 2001. Cumulative growing degree days (GDD) were calculated using local, daily maximum, and minimum air temperature data. A simple GDD model based on the formula GDD = (daily maximum temperature [C] + daily minimum temperature [C])/2, with a base temperature of 0 C and a starting point of January 1, was used to calculate cumulative GDD values for panicle sampling dates. Number of seed germinating per collected panicle was recorded in greenhouse germination tests. Estimations of degree days required for production of viable downy brome seed were made using nonlinear regression of germination on GDD. The GDD value at which viable seed can be found on plants (i.e., when seed germination > 0) was of interest. Estimates of the GDD values at which viable seed could be found in the three studies ranged from 582 GDD at Bozeman, MT, to 1,287 GDD at Stillwater, OK, with a group of GDD values for Pendleton and Pullman around 1,000. Variation in seed-set GDD among locations may be attributed to differing climatic conditions that control vernalization at the various locations or to differences in vernalization requirements among downy brome biotypes (or both).

Auxinic herbicides, such as 2,4-D and dicamba, that act as plant growth regulators are commonly used for broadleaf weed control in cereal crops (e.g., wheat, barley), grasslands, and noncroplands. If applied at late growth stages, while cereals are developing reproductive parts, the herbicides can reduce seed production. We tested whether growth regulators have this same effect on the invasive annual grass Japanese brome. The herbicides 2,4-D, dicamba, and picloram were applied at typical field use rates to Japanese brome at various growth stages in a greenhouse. Picloram reduced seed production nearly 100% when applied at the internode elongation, boot, or heading stages of growth, whereas dicamba appeared to be slightly less effective and 2,4-D was much less effective. Our results indicate it may be possible to control Japanese brome by using growth regulator herbicides to reduce its seed production, thereby depleting its short-lived seed bank.

The factual evidence for aquaporins, the constituents of water channels in cell membranes and operation of water channels is reviewed in developing, maturing and germinating seeds.

Assessments of seed storage physiology among Arecaceae (palm) species are often inconclusive because seeds exhibit diverse responses to low temperature and moisture conditions. Interrelationships between dry matter accumulation, cell structure and water relations during seed development of the endangered Hawaiian endemic palm, Pritchardia remota, suggest that damage from drying results from mechanical strain. Endosperm and fruits accumulate dry mass through most of the 400 d gestation period, but embryos reached maximum dry mass about 250 d post-anthesis (DPA). Mostly sucrose and some triacylglycerols accumulated in the cytoplasm and vacuoles of embryo cells, and organelles in mature embryo cells de-differentiated. Water content and water potential decreased as embryos matured and embryos contained about 0.45 g H2O (g dry mass)− 1 ( − 26 MPa) at shedding. Mature embryos survived drying to 0.16 g g− 1 ( − 49 MPa), but further drying was lethal. A model of allowable cell shrinkage is consistent with the substantial, but incomplete, desiccation tolerance acquired in P. remota embryos, and provides a new framework to explain variation in critical water contents as embryos develop. We suggest that desiccation tolerance, which distinguishes recalcitrant and orthodox physiologies among seeds, can be quantified by mechanical strain when embryo cells shrink during drying.

The potential longevity of japonica rice (Oryza sativa L. subsp. japonica) seed is particularly sensitive to high temperature – and thus climate change – during development and maturation. Cultivar Taipei 309 was grown at 28/20°C (12 h/12 h) and then from 19 DAA (days after 50% anthesis), when seeds were just over half filled, at 28/20°C, 30/22°C, 32/24°C or 34/26°C (12 h/12 h). Whereas ability to germinate ex planta had been achieved in almost all seeds by 24 DAA, only half the population were desiccation tolerant. Desiccation tolerance continued to increase over the subsequent 28 d, similarly at all four temperatures. Subsequent longevity, assessed by p50 (period in days to reduce viability to 50% in hermetic storage at 40°C with c. 15% moisture content), increased progressively at 28/20°C until 38 DAA, and remained constant until the final harvest (52 DAA). The three warmer temperature regimes provided similar longevity to 28/20°C at any one harvest, except at 38 DAA where the warmest (34/26°C) was poorer. That temperature regime also provided greater seed-to-seed variability within each survival curve. The results confirm that appreciable improvement in seed quality occurs during seed development and also subsequent maturation in japonica rice, but that increase in temperature from 28/20°C to 34/26°C during late seed filling onwards has comparatively little effect thereon. Comparison with previous investigations suggests that seed quality development may be less sensitive to high temperatures during late development and maturation than during the early seed development that precedes it.

We propose a novel approach to introducing hypothesis testing into the biologycurriculum. Instead of telling students the hypothesis and what kind of data to collectfollowed by a rigid recipe of testing the hypothesis with a given test statistic, we askstudents to develop a hypothesis and a mathematical model that describes the nullhypothesis. Simulation of the model under the null hypothesis allows students to comparetheir experimental data to what they would expect under the null hypothesis, thus leadingto a much more intuitive understanding of hypothesis testing. This approach has beentested both in the classroom and in faculty workshops, and we provide some suggestions forimplementations based on our experiences.

Starch is globally important as a source of food and, in addition, has a wide range of industrial applications. Much of this agriculturally produced starch is synthesized in developing seeds, where its biological function is to provide energy for seedling establishment. Storage starch in developing seeds is synthesized in heterotrophic plastids called amyloplasts and is distinct from the transient synthesis of starch in chloroplasts. This article reviews our current understanding of storage starch biosynthesis occurring in these organelles and discusses recent advances in research in this field. The review discusses starch structure and granule initiation, emerging ideas on the evolution of the pathway, the enzymes of starch synthesis, and the post-translational modification and regulation of key enzymes of amylopectin biosynthesis.