Seasonal Growth Cessation Research Articles

Age-dependent seasonal growth cessation in Populus.

In temperate and boreal regions, perennial plants adapt their annual growth cycle to the change of seasons. In natural forests, juvenile seedlings usually display longer growth seasons compared to adult trees to ensure their establishment and survival under canopy shade. However, how trees adjust their annual growth according to their age is not known. In this study, we show that age-dependent seasonal growth cessation is genetically controlled and found that the miR156-SPL3/5 module, a key regulon of vegetative phase change (VPC), also triggers age-dependent growth cessation in Populus trees. We show that miR156 promotes shoot elongation during vegetative growth, and its targets SPL3/5s function in the same pathway but as repressors. We find that the miR156-SPL3/5s regulon controls growth cessation in both leaves and shoot apices and through multiple pathways, but with a different mechanism compared to how the miR156-SPL regulon controls VPC in annual plants. Taken together, our results reveal an age-dependent genetic network in mediating seasonal growth cessation, a key phenological process in the climate adaptation of perennial trees.

A metabolic daylength measurement system mediates winter photoperiodism in plants.

Plants have served as a preeminent study system for photoperiodism due to their propensity to flower in concordance with the seasons. A nearly singular focus on understanding photoperiodic flowering has prevented the discovery of other photoperiod measuring systems necessary for vegetative health. Here, we use bioinformatics to identify photoperiod-induced genes in Arabidopsis. We show that one, PP2-A13, is expressed exclusively in, and required for, plant fitness in short, winter-like photoperiods. We create a real-time photoperiod reporter, using the PP2-A13 promoter driving luciferase, and show that photoperiodic regulation is independent of the canonical CO/FT mechanism for photoperiodic flowering. We then reveal that photosynthesis combines with circadian-clock-controlled starch production to regulate cellular sucrose levels to control photoperiodic expression of PP2-A13. This work demonstrates the existence of a photoperiod measuring system housed in the metabolic network of plants that functions to control seasonal cellular health.

Phytochrome B and PHYTOCHROME INTERACTING FACTOR8 modulate seasonal growth in trees.

The seasonally synchronized annual growth cycle that is regulated mainly by photoperiod and temperature cues is a crucial adaptive strategy for perennial plants in boreal and temperate ecosystems. Phytochrome B (phyB), as a light and thermal sensor, has been extensively studied in Arabidopsis. However, the specific mechanisms for how the phytochrome photoreceptors control the phenology in tree species remain poorly understood. We characterized the functions of PHYB genes and their downstream PHYTOCHROME INTERACTING FACTOR (PIF) targets in the regulation of shade avoidance and seasonal growth in hybrid aspen trees. We show that while phyB1 and phyB2, as phyB in other plants, act as suppressors of shoot elongation during vegetative growth, they act as promoters of tree seasonal growth. Furthermore, while the Populus homologs of both PIF4 and PIF8 are involved in the shade avoidance syndrome (SAS), only PIF8 plays a major role as a suppressor of seasonal growth. Our data suggest that the PHYB-PIF8 regulon controls seasonal growth through the regulation of FT and CENL1 expression while a genome-wide transcriptome analysis suggests how, in Populus trees, phyB coordinately regulates SAS responses and seasonal growth cessation.

Branching Regulator BRC1 Mediates Photoperiodic Control of Seasonal Growth in Hybrid Aspen

Cessation of growth as winter approaches is a key adaptive trait for survival of perennial plants, such as long-lived trees native to boreal and temperate regions [1, 2]. The timing of growth cessation in these plants is controlled by photoperiodic cues. As shown recently, perception of growth-repressive short photoperiod (SP) mediated via components of circadian clock results indownregulation of the tree ortholog of Arabidopsis flowering regulator FLOWERING LOCUS T(FT), FT2[3, 4]. Downregulation of FT2 results in suppression of downstream components LAP1 (orthologousto the Arabidopsis floral meristem identity gene APETALA1) and AIL1 (orthologous to AINTEGUMENTA in Arabidopsis), culminating in induction of growth cessation and bud set [5-7]. Results presented here reveal that, in addition to the CO/FT pathway, a photoperiodically controlled negative feedback loop involving a tree ortholog of Arabidopsis BRANCHED1 (BRC1) (a member of TEOSINTE BRANCHED 1, CYCLOIDEA, PCF family), LAP1, and FT2 participates in regulation of seasonal growth in the model tree hybrid aspen. In growth-promotive long photoperiod, LAP1 suppresses expression of BRC1, but upon perception of growth-repressive SP, downregulation of LAP1 de-represses expression of its downstream target BRC1. BRC1 physically interacts with FT2, and BRC1-FT interaction further reinforces the effect of SP and triggers growth cessation by antagonizing FT action. Accordingly, BRC1 gain and loss of function result in early and retarded growth cessation responses to SP, respectively. Thus, these results reveal a regulatory feedback loop that reinforces responses to SP and induction of seasonal growth cessation.

Modelling Populus autumn phenology: The importance of temperature and photoperiod

In late summer-early autumn, trees undergo growth cessation culminating in bud set. For a wide range of plants, including Populus, photoperiod is considered as the primary environmental cue determining timing of growth cessation and shoot to bud transition. However, studies on Populus have revealed temperature influence on seasonal growth cessation and bud set. In this study we examine the role of temperature in regulating the transition between phenological stages of bud development, from a growing apex to a closed bud. We test different model structures incorporating cues from both temperature and photoperiod (M1 and M2) as compared to the previously established model based on photoperiod only (M0, null hypothesis). All models simulate the date of bud set for Populus trees from 12 latitudinal populations grown in the common garden of Sävar. For two of the three years (2005 and 2007) M1 and M2 models outperformed the null model in predicting bud set date. Poor predictions for 2006 were related to stressful weather conditions. This indicates that under non-stressful conditions temperature can be a factor modifying the photoperiod response, while other regulatory mechanisms can be at play during stressful conditions. A phenological model of bud development has to account for both types of responses. Thus, our study highlights the importance of temperature as a factor that should be considered in addition to the well-established photoperiodic signal in studies on autumnal bud set under natural conditions.

Constitutive expression of the Poplar FD-like basic leucine zipper transcription factor alters growth and bud development.

In poplar, the CO/FT regulatory module mediates seasonal growth cessation. Although FT interacts with the basic leucine zipper transcription factor FD, surprisingly little is known about the possible role of FD in bud development and growth cessation in trees. In this study, we examined the expression and localization of the poplar FD homolog, PtFD1, during short-day (SD)-induced bud development, and the consequences of overexpressing PtFD1 on bud development and shoot growth. PtFD1 was primarily expressed in apical and axillary buds and exhibited a transient increase in expression during the initial stages of SD-induced bud development. This transient increase declined with continued SD treatment. When PtFD1 was overexpressed in poplar, SD-induced growth cessation and bud formation were abolished. PTFD1 overexpression also resulted in precocious flowering of juvenile plants in long-day (LD) photoperiods. Because the phenotypes associated with overexpression of PtFD1 are similar to those observe when poplar FT1 is overexpressed (Science, 312, 2006, 1040), the expression and diurnal patterns of expression of both poplar FT1 and FT2 were characterized in PtFD1 overexpression poplars and found to be altered. DNA microarray analysis revealed few differences in gene expression between PtFD1 overexpressing poplars in LD conditions while extensive levels of differential gene expression occur in SD-treated plants. These results enforce the connection between the regulation of flowering and the regulation of growth cessation and bud development in poplar.

Dormancy Interferes with Flowering in Perennial Plants with Short Day Regulation of Both Processes: A Mini-Review

In many perennial woody plants growing in the temperate and cold regions, regulation of seasonal growth cessation and floral initiation are closely integrated, both taking place in photoperiods shorter than a critical length. In the temperate shrub black currant (Ribes nigrum L.), the two processes proceed harmoniously in parallel under naturally decreasing autumn photoperiods, whereas an abrupt shift to photoperiods well below the critical length results in an immediate growth cessation and premature dormancy. As a result, floral initiation is suppressed and arrested. Other perennial plants such as hop (Humulus lupulus), which have the same dual short day responses, behave in the same way. In such plants, optimal flowering takes place at near-critical photoperiods, which are short enough to induce flowering and still long enough to prevent premature dormancy. These responses deviate from the situation in annual plants, which have predominated in studies on photoperiodic control of flowering. Another example of linkage between flowering and dormancy responses is the well-known dual effects of chilling temperature on vernalization and its relation to dormancy. Elucidation and disentangling of these networks of integrated processes are now awaiting joint research efforts in the areas of molecular genetics and experimental plant physiology.

A Tree Ortholog of APETALA1 Mediates Photoperiodic Control of Seasonal Growth

Photoperiodic control of development plays a key role in adaptation of plants to seasonal changes. A signaling module consisting of CONSTANS (CO) and FLOWERING LOCUS T (FT) mediates in photoperiodic control of a variety of developmental transitions (e.g., flowering, tuberization, and seasonal growth cessation in trees). How this conserved CO/FT module can mediate in the photoperiodic control of diverse unrelated developmental programs is poorly understood. We show that Like-AP1 (LAP1), a tree ortholog of Arabidopsis floral meristem identity gene APETALA1 (AP1), mediates in photoperiodic control of seasonal growth cessation downstream of the CO/FT module in hybrid aspen. Using LAP1 overexpressors and RNAi-suppressed transgenic trees, we demonstrate that short day (SD)-mediated downregulation of LAP1 expression is required for growth cessation. In contrast with AP1 targets in flowering, LAP1 acts on AINTEGUMENTA-like 1 transcription factor, which is implicated in SD-mediated growth cessation. Intriguingly, unlike AP1 in Arabidopsis, ectopic expression of LAP1 fails to induce early flowering in hybrid aspen trees. These results indicate that AP1 ortholog in trees has acquired a novel function in photoperiodic regulation of seasonal growth. Thus, photoperiodic signaling pathway may have diverged downstream of AP1/LAP1 rather than the CO/FT module during evolution. Moreover, control of flowering by the CO/FT module can be uncoupled from its role in photoperiodic control of seasonal growth in trees. Thus, our findings can explain mechanistically how a conserved signaling module can mediate in the control of a highly diverse set of developmental transitions by a similar input signal, namely photoperiod.

Potato CONSTANS is involved in photoperiodic tuberization in a graft‐transmissible manner

CONSTANS (CO) is involved in the photoperiodic control of plant developmental processes, including flowering in several species and seasonal growth cessation and bud set in trees. It has been proposed that CO could also affect the day-length regulation of tuber induction in Solanum tuberosum (potato), a plant of great agricultural relevance. To address this question, we examined the role of CO in potato. A potato CO-like gene, StCO, was identified and found to be highly similar to a previously reported potato gene of unknown function. Potato plants overexpressing StCO tuberized later than wild-type plants under a weakly inductive photoperiod. StCO silencing promoted tuberization under both repressive and weakly inductive photoperiods, but did not have any effect under strongly inductive short days, demonstrating that StCO represses tuberization in a photoperiod-dependent manner. The effect of StCO on tuber induction was transmitted through grafts. In addition, StCO affected the mRNA levels of StBEL5 - a tuberization promoter, the mRNA of which moves long distances in potato plants - and StFT/StSP6A, a protein highly similar to FLOWERING LOCUS T (FT), which is a key component of systemic flowering signals in other species. We also found that StFT/StSP6A transcript levels correlate with the induction of tuber formation in wild-type plants. These results show that StCO plays an important role in photoperiodic tuberization and, together with the recent demonstration that StFT/StSP6A promotes tuberization, indicate that the CO/FT module participates in controlling this process. Moreover, they support the notion that StCO is involved in the expression of long-distance regulatory signals in potato, as CO does in other species.

Seasonal Growth of Free-Ranging Gila Monsters (Heloderma suspectum) in a Southern Arizona Population

We fit asymptotic models to growth data of free-ranging Gila Monsters studied near Tucson, Arizona. We used a mixed-effects modeling procedure that allows for unequal numbers of recaptures by accounting for within-individual covariance and models between-individual variation in growth parameters as random effects. A model selection procedure and diagnostic tests indicated that a von Bertalanffy curve with seasonal cessation of growth and a random effect for asymptotic size fit the data best. Young Gila Monsters in our study grew faster than previously reported growth rates from both field and captive animals, and we discuss potential reasons for this discrepancy.

The expression of VvPHYA and VvPHYB transcripts is differently regulated by photoperiod in leaves and buds of grapevines

Light signals perceived by phytochromes (Phys) and cryptochromes (Crys) play key roles in plant growth and development and in photoperiod dependant process such as flowering, tuberization, seasonal growth cessation and dormancy. The integration of the light signals with the endogenous circadian oscillator provides plants with a mechanism to monitor changes in photoperiod or day-length. In a recent report, we established that in Vitis vinifera L. cv Thompson Seedless, photoperiod drives the entrance of buds into endodormancy (ED) and modifies the expression of VvPHYA and VvPHYB transcripts in grapevine leaves, suggesting that both VvPHYs could play crucial roles in SD-induced transition of bud into ED. Here, we aimed to establish whether the transition of grapevine buds into ED is a mere consequence of a decision taken in the leaf or whether the bud responds by itself to photoperiod. Results show that in defoliated grapevine canes, bud-ED development is delayed compared with non-defoliated control canes, and that under LD-photoperiod both VvPHYA and VvPHYB transcripts are highly expressed in grapevine buds, whilst under SD-photoperiod both VvPHYs are downregulated and expression can not be detected. Overall, the results suggest that grapevine bud behaves as semi-autonomous organ in sensing the photoperiod signal, and that VvPHYA and VvPHYB gene expression is differently regulated by photoperiod in leaf and bud of grapevines.

Plant research accelerates along the (bio)informatics superhighway

The Keystone Symposium on Plant Sensing, Response and Adaptation to the Environment took place between 11 and 16 January 2009, at Big Sky, Montana, USA, and was organized by S.A. Kay & J. Chory. ![][1] See Glossary for abbreviations used in this article In spite of the fanfare surrounding the two‐hundredth anniversary of the birth of Charles Darwin, and the one‐hundred and fiftieth anniversary of his most celebrated book ‘ On the Origin of Species ’ (Darwin, 1859), many people would still be surprised to learn that Darwin wrote a nearly 600 page book entitled ‘ The Power of Movement in Plants ’ (Darwin, 1880). As most plants have their location fixed as soon as their roots enter the soil, non‐specialists might wonder how much movement plants can make. However, movement is not limited to locomotion, and many of the movements studied by Darwin probably evolved in response to the unique challenges imposed by the rooted habit. Unable to change location, plants have developed exquisite abilities to sense, respond to and adapt to their local environment. One example that captured Darwin's attention is the navigation of the radicle (root) tip through the complex soil environment to optimize water and nutrient acquisition. He stated, “It is hardly an exaggeration to say that the tip of the radicle thus endowed, and having the power of directing the movements of the adjoining parts, acts like the brain of one of the lower animals[…].” These root‐growth movements were but one of many environmental responses discussed by plant biologists gathered at the recent Keystone Symposium on Plant Sensing, Response and Adaptation to the Environment. Root growth is controlled by gravity, water and nutrient acquisition; whereas growth of the aerial shoot is regulated primarily by the light environment. Various photoreceptors allow plants to judge light intensity, direction … [1]: /embed/graphic-1.gif

Wild Atlantic salmon Salmo salar L. strains have greater growth potential than a domesticated strain selected for fast growth

A study was undertaken to examine the responses of three Atlantic salmon Salmo salar strains to growth hormone (GH) treatment. A positive growth response to sustained‐release GH implants was found in two wild strains (Namsen and Imsa) as well as one domesticated strain (AquaGen). The data revealed that the growth‐selected AquaGen strain has further growth potential, however, a stronger growth response was observed in the wild strains which outgrew the domesticated strain after GH treatment. These observations suggest that some growth potential may have been lost during the selection for rapid growth in the AquaGen strain. In September, the parr were GH implanted and in December sampled for plasma GH and insulin‐like growth factor I (IGF‐I) levels, liver, muscle and gill GH receptor, IGF‐I mRNA levels, gill Na+,K+‐ATPase activity, muscle and liver lipid content and body silvering. Low temperature and seasonal growth cessation probably explains the relatively limited GH effects found. Body silvering in all strains was positively correlated to size. GH increased IGF‐I plasma levels in the Namsen strain inspite of liver IGF‐I mRNA levels being lower in GH‐treated fish.

Controlling the Coming of Catkins

The regulation of flowering in annual plants is controlled by a pair of genes, FT and CO . Are similar genes also involved in regulating flowering time in trees? The juvenile phase in trees can last for decades before the first flower is formed. During this time, the tree is nonresponsive to environmental factors that potentially influence flowering time. Böhlenius et al. show that the FT ortholog from Populus trees (poplars, aspen, and cottonwoods) is a critical determinant of flowering time in trees. The poplar FT is also responsible for a completely different developmental process in trees, the timing of the short-day-induced growth cessation and bud set that occurs in the fall. H. Böhlenius, T. Huang, L. Charbonnel-Campaa, A. M. Brunner, S. Jansson, S. H. Strauss, O. Nilsson, CO/FT regulatory module controls timing of flowering and seasonal growth cessation in trees. Science 312 , 1040-1043 (2006). [Abstract] [Full Text]

CO/FT Regulatory Module Controls Timing of Flowering and Seasonal Growth Cessation in Trees

Forest trees display a perennial growth behavior characterized by a multiple-year delay in flowering and, in temperate regions, an annual cycling between growth and dormancy. We show here that the CO/FT regulatory module, which controls flowering time in response to variations in daylength in annual plants, controls flowering in aspen trees. Unexpectedly, however, it also controls the short-day-induced growth cessation and bud set occurring in the fall. This regulatory mechanism can explain the ecogenetic variation in a highly adaptive trait: the critical daylength for growth cessation displayed by aspen trees sampled across a latitudinal gradient spanning northern Europe.

Evaluation of a mechanical dispenser and interplant bridges on the dispersal and efficacy of the predator, Phytoseiulus persimilis (Acari: Phytoseiidae) in greenhouse cut roses

Abstract Adequate distribution of natural enemies is necessary for successful augmentative biological control. In California greenhouse cut roses produced using the bent shoot system, the predatory mite Phytoseiulus persimils is widely used for control of the phytophagous mite Tetranychus urticae. One purported advantage of the bent shoot method is that the dense foliage of the lower canopy creates interplant bridges that facilitate predator movement. However, gaps in lower canopy interplant contact can occur in young plants or can result from varietal growth habit or seasonal cessation of growth in established plants. We observed an average of 1.63 ± 0.10 interplant contacts in the lower canopy across five rose varieties, with the average lower canopy gap being 3.52 ± 0.42 cm wide. We evaluated the use of interplant bridges of plastic flagging tape as a method to enhance dispersal of the P. persimilis predator. We determined that about three times as many predators moved from the plant on which they were released to adjacent plants when those plants were connected by bridges compared to those that were not. Finally, we tested the use of interplant bridges and a mechanical dispenser to determine if the use of a dispersal aid could enhance the efficacy of biological control. After 3 weeks in the greenhouse the number of leaves infested with T. urticae was reduced by approximately 50% using interplant bridges or a mechanical dispenser in comparison to controls without dispersal aid, although there was no difference between dispersal methods.

A new model accounting for seasonal cessation of growth in fishes

A modified version of the von Bertalanffy growth function (VBGF) is proposed in which a sine wave modifies a standard version of the VBGF, enabling a smooth transition between rapid summer growth and a variable period of zero growth (in length) during winter or during the dry season for aestivating fishes. The key features of a nonlinear routine for fitting this new model are also presented, with emphasis on the estimation of the period of zero growth. Application examples, to Salmo salar and Trisopterus esmarkii, are presented.

Crassula helmsii (T. Kirk) cockayne: Is it an aggressive alien aquatic plant in Britain?

The occurrence of this alien aquatic macrophyte has rapidly increased during the last decade reaching c. 100 sites mainly in England; these range from shallow acidic seasonal pools to small, more alkaline, nutrient-rich lakes. It is frequently dominant and can grow in an emergent form from 0·7m above the water to a submerged form 1·3m in length, to depths of c. 3m. Plant bimass is generally high with little seasonal cessation of growth. The habit is frequently a dense sward growth which smothers out other flora; it is present in c. ten reserves and is causing concern. It is widely available from aquatic suppliers, it has an enormous potential to propagate from small fragments and has a high growth rate. It is associated with soft sediments and possibly iron-rich areas; this is confirmed by growth trials in static water tanks. In flowing water trials, growth was even faster in water velocities up to 0·32 m s −1, indicating its potential—although no river sites in Britain are yet known. Control by physical removal, often recommended, results in numerous propagules and should be combined with a secondary technique. This initial study suggests that this plant will remain a problem and caution is required to prevent its further spread. Studies of techniques for its control are needed.

Studies on the Growth of Red Mangrove (Rhizophora mangle L.) 3. Phenology of the Shoot

Studies on the Growth of Red Mangrove (Rhizophora mangle L.) 3. Phenology of the Shoot

Deterministic models of living and fossil populations of animals

The factors influencing the size-frequency distribution of living and dead populations of organisms are discussed. They include kind of recruitment (even recruitment, a broad wave of recruitment, a sharp wave of recruitment, and two waves of recruitment during the year); growth-rate (linear, high-to-low as in many invertebrates, and high-to-zero as in vertebrates) ; different coefficients of variation in the growth-rate; mortality rate (constant, increasing, and decreasing); and seasonal cessation of growth, with or without increased mortality. Forty-two steady-state experiments using different combinations and permutations of these variables have been run in a computer and the results expressed as size-frequency graphs of the living and resulting dead populations. The graphs are intended to be used as an aid to the interpretation of size-frequency in living and fossil populations of animals. It is shown that the growth-rate and the mortality rate are the major factors influencing the primary shape of the size-frequency distribution in living and dead populations. Secondary peaks may be developed as a consequence of seasonal recruitment accompanied by seasonal cessation of growth, with or without increased mortality. The difficulties of interpreting mass mortality in fossil populations are discussed.