Sleeping but not defenseless: seed dormancy and protection.

To ensure their vital role in disseminating the species, dormant seeds have developed adaptive strategies to protect themselves against pathogens and predators. This is orchestrated through the synthesis of an array of constitutive defenses that are put in place in a developmentally regulated manner, which are the focus of this review. We summarize the defense activity and the nature of the molecules coming from the exudate of imbibing seeds that leak into its vicinity, also referred to as the spermosphere. As a second layer of protection, the dual role of the seed coat will be discussed; as a physical barrier and a multi-layered reservoir of defense compounds that are synthesized during seed development. Since imbibed dormant seeds can persist in the soil for extended times, we address the question if during this period, a constitutively regulated defense program is switched on to provide further protection, using the well-defined pathogenesis-related (PR) protein family. In addition, we review the hormonal and signaling pathways that might be involved in the interplay between dormancy and defense and point out questions that need further attention.

Plant Quiescence Strategy and Seed Dormancy under Hypoxia.

Plant quiescence and seed dormancy can be triggered by reduced oxygen availability. Under water, oxygen depletion caused by flooding can culminate in a quiescent state, which is a plant strategy for energy preservation and survival. In adult plants, a quiescent state can be activated by sugar starvation, culminating in metabolic depression. In seeds, secondary dormancy can be activated by reduced oxygen availability, which creates an unfavourable state for germination. The physical dormancy of some seeds and buds includes barriers to external conditions, which indirectly results in hypoxia. The molecular processes that support seed dormancy and plant survival through quiescence under hypoxia include the N-degron pathway, which enables the modulation of ethylene responsive factors of group VII and downstream targets. This oxygen- and nitric oxide-dependent mechanism interacts with phytohormone-related pathways to control growth.

The inability of barley to germinate after submergence depends on hypoxia-induced secondary dormancy.

Global climate change has dramatically increased flooding events, which have a strong impact on crop production. Barley (Hordeum vulgare) is one of the most important cereals and its cultivation includes a broad range of different environments. We tested the capacity to germinate of a large barley panel after a short period of submergence followed by a period of recovery. We demonstrate that sensitive barley varieties activate underwater secondary dormancy because of a lower permeability to oxygen dissolved in water. In sensitive barley accessions, secondary dormancy is removed by nitric oxide donors. The results of a genome-wide association study uncovered a Laccase gene located in a region of significant marker-trait association that is differently regulated during grain development and plays a key role in this process. Our findings will help breeders to improve the genetics of barley, thereby increasing the capacity of seeds to germinate after a short period of flooding.

Unravelling the paradox in physically dormant species: elucidating the onset of dormancy after dispersal and dormancy-cycling.

BACKGROUND: For species that produce seeds with a water-impermeable coat, i.e. physical dormancy (PY), it has been widely recognized that (1) seeds shed at a permeable state cannot become impermeable after dispersal; and (2) dormancy-cycling, i.e. a permeable ↔ impermeable transition, does not occur. Given a tight relationship between moisture content and onset of seed-coat impermeability, seeds maturing at low relative humidity (RH) and occurring in a high-temperature environment are inferred to produce impermeable coats, and ex situ drying of permeable seeds can lead to the onset of impermeability. SCOPE AND CONCLUSION: It is proposed here that permeable seeds dispersed at low RH and in high-temperature soils might become impermeable due to continuous drying. Similarly, seeds with shallow PY dormancy (with higher moisture content immediately after becoming impermeable) can cycle back to a permeable state or absolute PY (complete dry state) when RH increases or decreases, respectively. A conceptual model is developed to propose that seeds from several genera of 19 angiosperm families at the time of natural dispersal can be (1) impermeable (dormant), i.e. primary dormancy; (2) impermeable (dormant) and become permeable (non-dormant) and then enter a dormant state in the soil, often referred to as secondary dormancy; (3) permeable (non-dormant) and become impermeable (dormant) in the soil, i.e. enforced dormancy; or (4) dormant or non-dormant, but cycle between permeable and non-permeable states depending on the soil conditions, i.e. dormancy-cycling, which is different from sensitivity-cycling occurring during dormancy break. It is suggested that this phenomenon could influence the dormancy-breaking pattern, but detailed studies of this are lacking.

In-Depth Proteomic Analysis of the Secondary Dormancy Induction by Hypoxia or High Temperature in Barley Grains.

In barley, incubation of primary dormant (D1) grains on water under conditions that do not allow germination, i.e. 30°C in air and 15°C or 30°C in 5% O2, induces a secondary dormancy (D2) expressed as a loss of the ability to germinate at 15°C in air. The aim of this study was to compare the proteome of barley embryos isolated from D1 grains and D2 ones after induction of D2 at 30°C or in hypoxia at 15°C or 30°C. Total soluble proteins were analyzed by 2DE gel-based proteomics, allowing the selection of 130 differentially accumulated proteins (DAPs) among 1,575 detected spots. According to the protein abundance profiles, the DAPs were grouped into six abundance-based similarity clusters. Induction of D2 is mainly characterized by a down-accumulation of proteins belonging to cluster 3 (storage proteins, proteases, alpha-amylase inhibitors and histone deacetylase HD2) and an up-accumulation of proteins belonging to cluster 4 (1-Cys peroxiredoxin, lipoxygenase2 and caleosin). The correlation-based network analysis for each cluster highlighted central protein hub. In addition, most of genes encoding DAPs display high co-expression degree with 19 transcription factors. Finally, this work points out that similar molecular events accompany the modulation of dormancy cycling by both temperature and oxygen, including post-translational, transcriptional and epigenetic regulation.

Cold-induced secondary dormancy and its regulatory mechanisms in Beta vulgaris.

The dynamic behaviour of seeds in soil seed banks depends on their ability to act as sophisticated environmental sensors to adjust their sensitivity thresholds for germination by dormancy mechanisms. Here we show that prolonged incubation of sugar beet fruits at low temperature (chilling at 5°C, generally known to release seed dormancy of many species) can induce secondary nondeep physiological dormancy of an apparently nondormant crop species. The physiological and biophysical mechanisms underpinning this cold-induced secondary dormancy include the chilling-induced accumulation of abscisic acid in the seeds, a reduction in the embryo growth potential and a block in weakening of the endosperm covering the embryonic root. Transcriptome analysis revealed distinct gene expression patterns in the different temperature regimes and upon secondary dormancy induction and maintenance. The chilling caused reduced expression of cell wall remodelling protein genes required for embryo cell elongation growth and endosperm weakening, as well as increased expression of seed maturation genes, such as for late embryogenesis abundant proteins. A model integrating the hormonal signalling and master regulator expression with the temperature-control of seed dormancy and maturation programmes is proposed. The revealed mechanisms of the cold-induced secondary dormancy are important for climate-smart agriculture and food security.

Comprehensive profiling of alternative splicing landscape during secondary dormancy in oilseed rape (Brassica napus L.).

Alternative splicing is a general mechanism that regulates gene expression at the post-transcriptional level, which increases the transcriptomic diversity. Oilseed rape (Brassica napus L.), one of the main oil crops worldwide, is prone to secondary dormancy. However, how alternative splicing landscape of oilseed rape seed changes in response to secondary dormancy is unknown. Here, we analyzed twelve RNA-seq libraries from varieties "Huaiyou-SSD-V1" and "Huaiyou-WSD-H2" which exhibited high (> 95%) and low (< 5%) secondary dormancy potential, respectively, and demonstrated that alternative splicing changes led to a significant increase with the diversity of the transcripts in response to secondary dormancy induction via polyethylene glycol 6000 (PEG6000) treatment. Among the four basic alternative splicing types, intron retention dominates, and exon skipping shows the rarest frequency. A total of 8% of expressed genes had two or more transcripts after PEG treatment. Further analysis revealed that global isoform expression percentage variations in alternative splicing in differently expressed genes (DEGs) is more than three times as much as those in non-DEGs, suggesting alternative splicing change is associated with the transcriptional activity change in response to secondary dormancy induction. Eventually, 342 differently spliced genes (DSGs) associated with secondary dormancy were identified, five of which were validated by RT-PCR. The number of the overlapped genes between DSGs and DEGs associated with secondary dormancy was much less than that of either DSGs or DEGs, suggesting that DSGs and DEGs may independently regulates secondary dormancy. Functional annotation analysis of DSGs revealed that spliceosome components are overrepresented among the DSGs, including small nuclear ribonucleoprotein particles (snRNPs), serine/arginine-rich (SR) proteins, and other splicing factors. Thus, it is proposed that the spliceosome components could be exploited to reduce secondary dormancy potential in oilseed rape. Supplementary Information: The online version contains supplementary material available at 10.1007/s11032-022-01314-8.

Lipophilic signals lead to organ-specific gene expression changes in Arabidopsis seedlings.

In plants, N-acylethanolamines (NAEs) are most abundant in desiccated seeds and their levels decline during germination and early seedling establishment. However, endogenous NAE levels rise in seedlings when ABA or environmental stress is applied, and this results in an inhibition of further seedling development. When the most abundant, polyunsaturated NAEs of linoleic acid (18:2) and linolenic acid (18:3) were exogenously applied, seedling development was affected in an organ-specific manner. NAE 18:2 primarily affected primary root elongation and NAE 18:3 primarily affected cotyledon greening and expansion and overall seedling growth. The molecular components and signaling mechanisms involved in this pathway are not well understood. In addition, the bifurcating nature of this pathway provides a unique system in which to study the spatial aspects and interaction of these lipid-specific and organ-targeted signaling pathways. Using whole transcriptome sequencing (RNA-seq) and differential expression analysis, we identified early (1-3 hr) transcriptional changes induced by the exogenous treatment of NAE 18:2 and NAE 18:3 in cotyledons, roots, and seedlings. These two treatments led to a significant enrichment in ABA-response and chitin-response genes in organs where the treatments led to changes in development. In Arabidopsis seedlings, NAE 18:2 treatment led to the repression of genes involved in cell wall biogenesis and organization in roots and seedlings. In addition, cotyledons, roots, and seedlings treated with NAE 18:3 also showed a decrease in transcripts that encode proteins involved in growth processes. NAE 18:3 also led to changes in the abundance of transcripts involved in the modulation of chlorophyll biosynthesis and catabolism in cotyledons. Overall, NAE 18:2 and NAE 18:3 treatment led to lipid-type and organ-specific gene expression changes that include overlapping and non-overlapping gene sets. These data will provide future, rich opportunities to examine the genetic pathways involved in transducing early signals into downstream physiological changes in seedling growth.

Dormancy cycling is accompanied by changes in ABA sensitivity in Polygonum aviculare seeds.

Polygonum aviculare seeds show high levels of primary dormancy (PD). Low winter temperatures alleviate dormancy and high spring temperatures induce seeds into secondary dormancy (SD), naturally establishing stable seedbanks cycling through years. The objective of this work was to elucidate the mechanism(s) involved in PD expression and release, and in SD induction in these seeds, and the extent to which abscisic acid (ABA) and gibberellins (GAs) are part of these mechanisms. Quantification of endogenous ABA both prior to and during incubation, and sensitivity to ABA and GAs, were assessed in seeds with contrasting dormancy. Expression analysis was performed for candidate genes involved in hormone metabolism and signaling. It was found that endogenous ABA content does not explain either dormancy release or dormancy induction; moreover, it does not seem to play a role in dormancy maintenance. However, dormancy modifications were commonly accompanied by changes in ABA sensitivity. Concomitantly, induction into SD, but not PD, was characterized by a increased PaABI-5 and PaPYL transcription, and a rise in GA sensitivity as a possible counterbalance effect. These results suggest that dormancy cycling in this species is related to changes in embryo sensitivity to ABA; however, this sensitivity appears to be controlled by different molecular mechanisms in primary and secondary dormant seeds.

Breaking Seed Dormancy during Dry Storage: A Useful Tool or Major Problem for Successful Restoration via Direct Seeding?

To facilitate the restoration of disturbed vegetation, seeds of wild species are collected and held in dry storage, but often there is a shortage of seeds for this purpose. Thus, much research effort is expended to maximize the use of the available seeds and to ensure that they are nondormant when sown. Sowing nondormant (versus dormant) seeds in the field should increase the success of the restoration. Of the various treatments available to break seed dormancy, afterripening, that is, dormancy break during dry storage, is the most cost-effective. Seeds that can undergo afterripening have nondeep physiological dormancy, and this includes members of common families such as Asteraceae and Poaceae. In this review, we consider differences between species in terms of seed moisture content, temperature and time required for afterripening and discuss the conditions in which afterripening is rapid but could lead to seed aging and death if storage is too long. Attention is given to the induction of secondary dormancy in seeds that have become nondormant via afterripening and to the biochemical and molecular changes occurring in seeds during dry storage. Some recommendations are made for managing afterripening so that seeds are nondormant at the time for sowing. The most important recommendation probably is that germination responses of the seeds need to be monitored for germinability/viability during the storage period.

Seed germination in Narcissus yepesii (Amaryllidaceae): clinal variation in the morphophysiological dormancy levels.

Seed dormancy classes determine both population and species-level processes which can be crucial in the life cycle of many plants. However, there are no studies of a dormancy cline between levels of morphophysiological dormancy (MPD). We aimed to determine the class of seed dormancy of Narcissus yepesii exhibits in order to explore links between different dormancy levels, previously characterized in two closely related phylogenetic congeners, N. alcaracensis and N. longispathus. Experiments were carried out under both near-natural temperature and controlled laboratory conditions. The parameters calculated were mean embryo length, radicle and shoot emergence percentages. The effects of different periods of storage; and different periods with or without GA3 of warm, cold or warm plus cold were analysed. The Narcissus populations from the Baetic System of mountain ranges in south-eastern Spain show clinal variation in a northeast-southwest gradient from intermediate to non-deep complex MPD, through the coexistence of intermediate and non-deep complex MPD in N. yepesii (21 % and 74 %, respectively). In addition, 54 % of stored seeds were able to show both levels of MPD. Narcissus yepesii occupies an intermediate position between N. alcaracensis and N. longispathus in the geographical distribution and in the clinal germination ranges. It strongly suggests an evolutionary gradient, which connects the intermediate complex MPD with the non-deep complex MPD in southern Iberian daffodils. This is the first study showing a gradient in the evolution between levels of MPD. Our results demonstrate a cline in these levels in response to both an environmental gradient and genetic differences.

Dormancy cycling: translation-related transcripts are the main difference between dormant and non-dormant seeds in the field.

Primary seed dormancy is a mechanism that orchestrates the timing of seed germination in order to prevent out-of-season germination. Secondary dormancy can be induced in imbibed seeds when they encounter prolonged unfavourable conditions. Secondary dormancy is not induced during dry storage, and therefore the mechanisms underlying this process have remained largely unexplored. Here, a 2-year seed burial experiment in which dormancy cycling was studied at the physiological and transcriptional level is presented. For these analyses six different Arabidopsis thaliana genotypes were used: Landsberg erecta (Ler) and the dormancy associated DELAY OF GERMINATION (DOG) near-isogenic lines 1, 2, 3, 6 and 22 (NILDOG1, 2, 3, 6 and 22). The germination potential of seeds exhumed from the field showed that these seeds go through dormancy cycling and that the dynamics of this cycling is genotype dependent. RNA-seq analysis revealed large transcriptional changes during dormancy cycling, especially at the time points preceding shifts in dormancy status. Dormancy cycling is driven by soil temperature and the endosperm is important in the perception of the environment. Genes that are upregulated in the low- to non-dormant stages are enriched for genes involved in translation, indicating that the non-dormant seeds are prepared for rapid seed germination.

Regulation of seed dormancy by the maternal environment is instrumental for maximizing plant fitness in Polygonum aviculare.

Emergence at an appropriate time and place is critical for maximizing plant fitness and hence sophisticated mechanisms such as seed dormancy have evolved. Although maternal influence on different aspects of dormancy behavior has been identified, its impact under field conditions and its relation to plant fitness has not been fully determined. This study examined maternal effects in Polygonum aviculare on release of seed primary dormancy, responses to alternating temperatures, induction into secondary dormancy, and field emergence patterns as influenced by changes in the sowing date and photoperiod experienced by the mother plant. Maternal effects were quantified using population threshold models that allowed us to simulate and interpret the experimental results. We found that regulation of dormancy in P. aviculare seeds by the maternal environment is instrumental for maximizing plant fitness in the field. This regulation operates by changing the dormancy level of seeds dispersed at different times (as a consequence of differences in the sowing dates of mother plants) in order to synchronize most emergence to the seasonal period that ultimately guarantees the highest reproductive output of the new generation. Our results also showed that maternal photoperiod, which represents a clear seasonal cue, is involved in this regulation.

A transcriptome analysis reveals a role for the indole GLS-linked auxin biosynthesis in secondary dormancy in rapeseed (Brassica napus L.).

BACKGROUND: Brassica napus L. has little or no primary dormancy, but exhibits great variation in secondary dormancy. Secondary dormancy potential in oilseed rape can lead to the emergence of volunteer plants that cause genetic contamination, reduced quality and biosafety issues. However, the mechanisms underlying secondary dormancy are poorly understood. In this study, cultivars Huaiyou-WSD-H2 (H) and Huaiyou-SSD-V1 (V), which exhibit low (approximately 5%) and high (approximately 95%) secondary dormancy rate, respectively, were identified. Four samples, before (Hb and Vb) and after (Ha and Va) secondary dormancy induction by polyethylene glycol (PEG), were collected to identify the candidate genes involved in secondary dormancy via comparative transcriptome profile analysis. RESULTS: A total of 998 differentially expressed genes (DEGs), which are mainly involved in secondary metabolism, transcriptional regulation, protein modification and signaling pathways, were then detected. Among these DEGs, the expression levels of those involved in the sulfur-rich indole glucosinolate (GLS)-linked auxin biosynthesis pathway were markedly upregulated in the dormant seeds (Va), which were validated by qRT-PCR and subsequently confirmed via detection of altered concentrations of indole-3-acetic acid (IAA), IAA conjugates and precursors. Furthermore, exogenous IAA applications to cultivar H enhanced secondary dormancy. CONCLUSION: This study first (to our knowledge) elucidated that indole GLS-linked auxin biosynthesis is enhanced during secondary dormancy induced by PEG, which provides valuable information concerning secondary dormancy and expands the current understanding of the role of auxin in rapeseed.

Temperature mediates secondary dormancy in resting cysts of Pyrodinium bahamense (Dinophyceae).

High-biomass blooms of the toxic dinoflagellate Pyrodinium bahamense occur most summers in Tampa Bay, Florida, USA, posing a recurring threat to ecosystem health. Like many dinoflagellates, P. bahamense forms immobile resting cysts that can be deposited on the seafloor-creating a seed bank that can retain the organism within the ecosystem and initiate future blooms when cysts germinate. In this study, we examined changes in the dormancy status of cysts collected from Tampa Bay and applied lessons from plant ecology to explore dormancy controls. Pyrodinium bahamense cysts incubated immediately after field collection displayed a seasonal pattern in dormancy and germination that matched the pattern of cell abundance in the water column. Newly deposited (surface) cysts and older (buried) cysts exhibited similar germination patterns, suggesting that a common mechanism regulates dormancy expression in new and mature cysts. Extended cool- and warm-temperature conditioning of field-collected cysts altered the cycle of dormancy compared with that of cysts in nature, with the duration of cool temperature exposure being the best predictor of when cysts emerged from dormancy. Extended warm conditioning, on the other hand, elicited a return to dormancy, or secondary dormancy, in nondormant cysts. These results directly demonstrate environmental induction of secondary dormancy in dinoflagellates-a mechanism common and thoroughly documented in higher plants with seasonal growth cycles. Our findings support the hypothesis that a seasonal cycle in cyst germination drives P. bahamense bloom periodicity in Tampa Bay and point to environmentally induced secondary dormancy as an important regulatory factor of that cycle.

Seed dormancy regulates germination response to smoke and temperature in a rhizomatous evergreen perennial.

Seed dormancy status regulates the response of seeds to environmental cues that can trigger germination. Anigozanthos flavidus (Haemodoraceae) produces seeds with morphophysiological dormancy (MPD) that are known to germinate in response to smoke, but embryo growth dynamics and germination traits in response to temperatures and after-ripening have not been well characterized. Seeds of A. flavidus, after-ripened for 28 months at 15 °C/15 % relative humidity, were incubated on water agar, water agar containing 1 µM karrikinolide (KAR1) or 50 µM glyceronitrile at 5, 10, 15, 20, 25, 20/10 and 25/15 °C for 28 days. After incubation at 5, 10 and 25 °C for 28 days, seeds were transferred to 15 °C for another 28 days. Embryo growth dynamics were tested at 5, 10, 15 and 25 °C. Results demonstrated that fresh seeds of A. flavidus had MPD and the physiological dormancy (PD) component could be broken by either glyceronitrile or dry after-ripening. After-ripened seeds germinated to ≥80 % at 15-20 °C while no additional benefit of germination was observed in the presence of the KAR1 or glyceronitrile. Embryo length significantly increased at 10 °C, and only slightly increased at 5 °C, while growth did not occur at 25 °C. When un-germinated seeds were moved from 5-10 °C to 15 °C for a further 28 days, germination increased from 0 to >80 % in significantly less time indicating that cold stratification may play a key role in the germination process during winter and early spring in A. flavidus. The lower germination (<50 %) of seeds moved from 25 to 15 °C was produced by the induction of secondary dormancy. Induction of secondary dormancy in seeds exposed to warm stratification, a first report for Anigozanthos species, suggests that cycling of PD may be an important mechanism of controlling germination timing in the field.

Germination and seed conservation of a pioneer species, Tecoma stans (Bignoniaceae), from tropical dry forest of Colombia / Germinación y conservación de semillas de la especie pionera, Tecoma stans (Bignoniaceae), del bosque seco tropical de Colombia

Abstract Seed germination and seed longevity under different environmental conditions are fundamental to understand the ecological dynamics of a species, since they are decisive for its success within the ecosystem. Taking this into account, seed germination and seed storage behavior of a pioneer species of tropical dry forest (Tecoma stans) were studied in the laboratory, to establish the effect of different environmental conditions on a local tree population. Two seed lots collected in July 2011, from Cali (Colombia), were evaluated under three alternating temperatures (20/30, 20/25, 25/30 ºC; 16/8 h) and four light qualities (12-hour white light photoperiod, darkness, and 15 minutes of red light -R and far red light -FR). Final germination was recorded for all treatments; for white light treatment the daily germination was recorded to calculate mean germination rate, mean germination time, and two synchronization indices. To assess the effect of light quality on physiological variables, a destructive germination test was carried out. For this test, another seed lot was evaluated under the same light conditions using an alternating temperature of 20/30 °C - 16/8 h, recording germination during six days for every treatment. In addition, seeds were stored at two different moisture contents (7.7, 4.1 %) and three storage temperatures (20, 5, -20 ºC), during two time periods (one and three months); a seed germination test was conducted for each treatment. Four replicates of 35 seeds per treatment were used for all experiments. Germination was high (GP > 90 %) with all alternating temperatures under white light, whereas under R, FR, and darkness germination was evenly successful at low temperatures, but at higher temperature, half of the seeds entered into secondary dormancy (GP= 45-65 %). However, mean germination rate and synchronization under R and FR decreased significantly in comparison to white light treatment and, consequently, mean germination time increased. Seed storage behavior of this species is orthodox due to the high germination (GP > 90 %) obtained under all treatments. In conclusion, T. stans seeds have a negative germination response at high incubation temperatures in the absence of white light, entering into a secondary dormancy. In contrast, an environment with a lower temperature and without white light delays the germination, but at the end seeds are able to reach the same germination values. This seed dependence on incident light in limiting conditions suggests a physiological mechanism on the seed tissues of this species, probably mediated by phytochromes. Finally, the orthodox seed storage behavior of T. stans is a reason to include this species in ex situ seed conservation programs for restoration and recovery of the tropical dry forest; however, long-term studies should be conducted in order to evaluate the maintenance of this characteristic throughout longer periods of time. Rev. Biol. Trop. 66(2): 918936. Epub 2018 June 01.

Resumen La germinación y la longevidad de las semillas de una especie bajo diferentes condiciones ambientales son fundamentales para las dinámicas ecológicas de una especie, debido a que son decisivas en el éxito de la misma en un ecosistema. Teniendo en cuenta esto, se estudió la germinación y el comportamiento en el almacenamiento de las semillas de una especie pionera de bosque seco tropical (Tecoma stans) a nivel de laboratorio, para establecer el efecto de diferentes condiciones ambientales en una población local de árboles. Dos lotes de semillas recolectados en julio 2011, de Cali (Colombia), se evaluaron a tres temperaturas alternadas (20 / 30, 20 / 25, 25 / 30 °C; 16 / 8 h) y cuatro calidades de luz (fotoperiodo de 12 horas de luz blanca, oscuridad, y 15 minutos de luz roja -R y roja lejana -RL). Se registró la germinación final para todos los tratamientos; para el tratamiento de luz blanca se registró la germinación diaria para calcular la tasa media de germinación, el tiempo medio de germinación y dos índices de sincronización. Para evaluar el efecto de la calidad de luz sobre las variables fisiológicas, se realizó una prueba de germinación destructiva. Para esta prueba, otro lote de semillas fue puesto a las mismas condiciones de luz usando una temperatura alternada de 20 / 30 °C - 16 / 8 h, registrando la germinación durante seis días para cada tratamiento. Además, se almacenaron semillas a dos contenidos de humedad (7.7, 4.1 %) y a tres temperaturas de almacenamiento (20, 5, -20 °C), durante dos periodos de tiempo (uno y tres meses); se realizó una prueba de germinación a cada tratamiento. Cuatro repeticiones de 35 semillas por cada tratamiento se usaron en cada experimento. La germinación fue alta (PG > 90 %) en todas las temperaturas alternadas con luz blanca, mientras que en los tratamientos de luz R, RL y en oscuridad, la germinación fue igualmente exitosa a bajas temperaturas, pero a temperaturas más altas la mitad de las semillas entraron en latencia secundaria (PG= 45-65 %). Sin embargo, la tasa media de germinación y la sincronización en R y RL disminuyeron significativamente en comparación con el tratamiento de luz blanca y consecuentemente el tiempo medio de germinación aumentó. El comportamiento de las semillas de T. stans en el almacenamiento es ortodoxo debido a la alta germinación obtenida (PG > 90 %) en todos los tratamientos. En conclusión, las semillas de T. stans tienen una respuesta germinativa negativa a temperaturas de incubación alta en ausencia de luz blanca, donde entran a latencia secundaria. En contraste, un ambiente con baja temperatura y sin luz blanca retrasa la germinación, pero al final las semillas son capaces de alcanzar los mismos valores de germinación. Esta dependencia de las semillas a la luz incidente en condiciones limitantes sugiere la presencia de un mecanismo fisiológico en los tejidos de esta especie, probablemente mediado por fitocromos. Finalmente, el comportamiento ortodoxo de las semillas de T. stans en el almacenamiento abre la posibilidad de incluirla en programas de conservación ex situ para la restauración y recuperación del bosque seco tropical; no obstante, se deben llevarse a cabo pruebas más largas para evaluar el mantenimiento de esta característica por periodos de tiempo más largos.

Within- and trans-generational plasticity: seed germination responses to light quantity and quality.

Plants respond not only to the environment in which they find themselves, but also to that of their parents. The combination of within- and trans-generational phenotypic plasticity regulates plant development. Plants use light as source of energy and also as a cue of competitive conditions, since the quality of light (ratio of red to far-red light, R:FR) indicates the presence of neighbouring plants. Light regulates many aspects of plant development, including seed germination. To understand how seeds integrate environmental cues experienced at different times, we quantified germination responses to changes in light quantity (irradiance) and quality (R:FR) experienced during seed maturation and seed imbibition in Arabidopsis thaliana genotypes that differ in their innate dormancy levels and after treatments that break or reinduce dormancy. In two of the genotypes tested, reduced irradiance as well as reduced R:FR during seed maturation induced higher germination; thus, the responses to light quantity and R:FR reinforced each other. In contrast, in a third genotype, reduced irradiance during seed maturation induced progeny germination, but response to reduced R:FR was in the opposite direction, leading to a very weak or no overall effect of a simulated canopy experienced by the mother plant. During seed imbibition, reduced irradiance and reduced R:FR caused lower germination in all genotypes. Therefore, responses to light experienced at different times (maturation vs. imbibition) can have opposite effects. In summary, seeds responded both to light resources (irradiance) and to cues of competition (R:FR), and trans-generational plasticity to light frequently opposed and was stronger than within-generation plasticity.

Germination, viability and longevity of horseweed (Conyza spp.) seeds as a function of temperature and evaluation periods / Germinação, viabilidade e longevidade de sementes de buva (Conyza spp.) em função da temperatura e períodos de avaliação

ABSTRACT: In Brazil, horseweed is one of the most important weeds because of the resistance to herbicides and high competitive for the crops. A large of losses were reported in major crops such as soybeans, wheat and corn, where the use a no-tillage system and the herbicide resistance promote better establishment. A correct understanding of the way temperature influences germination enables the prediction of the regions with the highest potential for colonization by this weed and thus facilitates its control. The objective of this study; therefore, was to discern the ways temperature affected the germination, viability and longevity of horseweed seeds. Testing was done at 10, 20 and 30°C, while evaluation occurred on days 0, 15, 30, 45 and 60. Seeds were packed in a nylon mesh bag (5x5cm), with 10g of upland soil (Yellow Red Argissolo, sandy loam texture), placed in transparent plastic boxes at 0 to 0.5cm soil depth, at the temperatures specified. Percentage of remaining seeds, first and second germination counts, abnormal seedlings, and dead, dormant, viable and non-viable seeds, were assessed. Horseweed seeds achieve secondary dormancy at 10, 20 and 30°C, while their quality and the longevity showed damage at 20 and 30°C temperatures.

RESUMO: No Brasil, a buva (Conyza spp.) é uma das principais plantas daninhas devido à resistência a herbicidas e alta competividade com as culturas. Esta é responsável por perdas de produtividade em culturas como soja, milho, algodão e trigo cuja implementação da semeadura direta e a resistência aos herbicidas favorecem seu estabelecimento. O conhecimento do efeito da temperatura na germinação permite prever as regiões com maior potencial de colonização e auxiliar no manejo. Assim, objetivou-se com este trabalho determinar o efeito da temperatura na germinação, viabilidade e longevidade de sementes de buva em solo de terras altas. As temperaturas testadas foram 10, 20 e 30ºC e os períodos de avaliação 0, 15, 30, 45 e 60 dias. As sementes foram acondicionadas em saco de malha de nylon (5 x 5cm), distribuídas em 10g de solo de terras altas (Argissolo Vermelho Amarelo, de textura franco-arenosa), e, alocadas em caixas gerbox com solo a profundidade de 0 a 0,5 cm, nas temperaturas descritas. Avaliou-se em percentagem de sementes remanescentes, primeira e segunda contagem de germinação, plântulas anormais, sementes mortas, dormentes, viáveis e não viáveis. A semente de buva atinge dormência secundária, nas temperaturas de 10, 20 e 30ºC e sua qualidade e longevidade são prejudicadas nas temperaturas de 20 e 30ºC.