Floral Budbreak Research Articles

Genetic and molecular regulation of chilling requirements in pear: breeding for climate change resilience.

Pear (Pyrus spp.) is a deciduous fruit tree that requires exposure to sufficient chilling hours during the winter to establish dormancy, followed by favorable heat conditions during the spring for normal vegetative and floral budbreak. In contrast to most temperate woody species, apples and pears of the Rosaceae family are insensitive to photoperiod, and low temperature is the major factor that induces growth cessation and dormancy. Most European pear (Pyrus Communis L.) cultivars need to be grown in regions with high chilling unit (CU) accumulation to ensure early vegetative budbreak. Adequate vegetative budbreak time will ensure suitable metabolite accumulation, such as sugars, to support fruit set and vegetative development, providing the necessary metabolites for optimal fruit set and development. Many regions that were suitable for pear production suffer from a reduction in CU accumulation. According to climate prediction models, many temperate regions currently suitable for pear cultivation will experience a similar accumulation of CUs as observed in Mediterranean regions. Consequently, the Mediterranean region can serve as a suitable location for conducting pear breeding trials aimed at developing cultivars that will thrive in temperate regions in the decades to come. Due to recent climatic changes, bud dormancy attracts more attention, and several studies have been carried out aiming to discover the genetic and physiological factors associated with dormancy in deciduous fruit trees, including pears, along with their related biosynthetic pathways. In this review, current knowledge of the genetic mechanisms associated with bud dormancy in European pear and other Pyrus species is summarized, along with metabolites and physiological factors affecting dormancy establishment and release and chilling requirement determination. The genetic and physiological insights gained into the factors regulating pear dormancy phase transition and determining chilling requirements can accelerate the development of new pear cultivars better suited to both current and predicted future climatic conditions.

Target enrichment sequencing coupled with GWAS identifies MdPRX10 as a candidate gene in the control of budbreak in apple.

The timing of floral budbreak in apple has a significant effect on fruit production and quality. Budbreak occurs as a result of a complex molecular mechanism that relies on accurate integration of external environmental cues, principally temperature. In the pursuit of understanding this mechanism, especially with respect to aiding adaptation to climate change, a QTL at the top of linkage group (LG) 9 has been identified by many studies on budbreak, but the genes underlying it remain elusive. Here, together with a dessert apple core collection of 239 cultivars, we used a targeted capture sequencing approach to increase SNP resolution in apple orthologues of known or suspected A. thaliana flowering time-related genes, as well as approximately 200 genes within the LG9 QTL interval. This increased the 275 223 SNP Axiom® Apple 480K array dataset by an additional 40 857 markers. Robust GWAS analyses identified MdPRX10, a peroxidase superfamily gene, as a strong candidate that demonstrated a dormancy-related expression pattern and down-regulation in response to chilling. In-silico analyses also predicted the residue change resulting from the SNP allele associated with late budbreak could alter protein conformation and likely function. Late budbreak cultivars homozygous for this SNP allele also showed significantly up-regulated expression of C-REPEAT BINDING FACTOR (CBF) genes, which are involved in cold tolerance and perception, compared to reference cultivars, such as Gala. Taken together, these results indicate a role for MdPRX10 in budbreak, potentially via redox-mediated signaling and CBF gene regulation. Moving forward, this provides a focus for developing our understanding of the effects of temperature on flowering time and how redox processes may influence integration of external cues in dormancy pathways.

Modeling the Budbreak in Peaches: A Basic Approach Using Chill and Heat Accumulation

Phenological shifts in peaches have been observed over the last few years due to the fluctuation of the seasonal climate conditions experienced during dormancy, affecting orchard management practices and influencing production and harvest dates. This study aimed to model the vegetative and floral budbreak of selected peach cultivars. Three peach cultivars, including “Rubyprince”, “Harvester”, and “Red Globe”, were considered in this study based on the representation of the early, early-mid, and mid-seasons. The prediction of the budbreak in peaches was assessed using different models that integrate the combination of chill and heat requirements. Models used include the Weinberger model, the modified Weinberger model, Utah, the dynamic model, and the growing degree model. The accumulation of chill varies according to the season evaluated. A model that considers both chill and heat accumulation is presented for each cultivar. Budbreak as an indicator of dormancy completion was established for each cultivar. The outcome of this study is to determine the amount of chilling accumulation and thermal time required to mark the beginning of the budbreak in selected cultivars with a model that predicts the duration of the dormancy. These results are valuable information that can be used for crop management practices and support the mitigation of cold damage during this critical period of crop development.

Molecular Cues for Phenological Events in the Flowering Cycle in Avocado.

Reproductively mature horticultural trees undergo an annual flowering cycle that repeats each year of their reproductive life. This annual flowering cycle is critical for horticultural tree productivity. However, the molecular events underlying the regulation of flowering in tropical tree crops such as avocado are not fully understood or documented. In this study, we investigated the potential molecular cues regulating the yearly flowering cycle in avocado for two consecutive crop cycles. Homologues of flowering-related genes were identified and assessed for their expression profiles in various tissues throughout the year. Avocado homologues of known floral genes FT, AP1, LFY, FUL, SPL9, CO and SEP2/AGL4 were upregulated at the typical time of floral induction for avocado trees growing in Queensland, Australia. We suggest these are potential candidate markers for floral initiation in these crops. In addition, DAM and DRM1, which are associated with endodormancy, were downregulated at the time of floral bud break. In this study, a positive correlation between CO activation and FT in avocado leaves to regulate flowering was not seen. Furthermore, the SOC1-SPL4 model described in annual plants appears to be conserved in avocado. Lastly, no correlation of juvenility-related miRNAs miR156, miR172 with any phenological event was observed.

Genome-wide identification and comparative analysis of DNA methyltransferase and demethylase gene families in two ploidy Cyclocarya paliurus and their potential function in heterodichogamy

BackgroundDNA methylation is one of the most abundant epigenetic modifications, which plays important roles in flower development, sex differentiation, and regulation of flowering time. Its pattern is affected by cytosine-5 DNA methyltransferase (C5-MTase) and DNA demethylase (dMTase). At present, there are no reports on C5-MTase and dMTase genes in heterodichogamous Cyclocarya paliurus.ResultsIn this study, 6 CpC5-MTase and 3 CpdMTase genes were identified in diploid (2n = 2 × = 32) C. paliurus, while 20 CpC5-MTase and 13 CpdMTase genes were identified in autotetraploid (2n = 4 × = 64). 80% of identified genes maintained relatively fixed positions on chromosomes during polyploidization. In addition, we found that some DRM subfamily members didn’t contain the UBA domain. The transcript abundance of CpC5-MTase and CpdMTase in male and female flowers of two morphs (protandry and protogyny) from diploidy was analyzed. Results showed that all genes were significantly up-regulated at the stage of floral bud break (S2), but significantly down-regulated at the stage of flower maturation (S4). At S2, some CpC5-MTase genes showed higher expression levels in PG-M than in PG-F, whereas some CpdMTase genes showed higher expression levels in PA-M than in PA-F. In addition, these genes were significantly associated with gibberellin synthesis-related genes (e.g. DELLA and GID1), suggesting that DNA methylation may play a role in the asynchronous floral development process through gibberellin signal.ConclusionsThese results broaden our understanding of the CpC5-MTase and CpdMTase genes in diploid and autotetraploid C. paliurus, and provide a novel insight into regulatory mechanisms of DNA methylation in heterodichogamy.

Ppe.CR.1 DNA test for predicting chilling requirement in peach

Chilling requirement (CR) is an important agronomic trait controlling the floral bud break for proper flowering in peach. Even though it has been widely researched and several peach CR quantitative trait loci (QTLs) have been identified, no diagnostic DNA tests validated in the U.S. peach breeding germplasm are available for this trait. Breeders and growers need a simple DNA test to predict the CR of peach cultivars for their particular environment. Therefore, we developed a quick and reliable Kompetitive Allele Specific PCR (KASP) DNA test using haplotype information from 9K IPSC genotype data of the U.S. peach germplasm integrating four CR-associated SNP markers from the previously reported CR QTL region on linkage group 1. Four KASP assays (Ppe.CR.1-1 to -4) were developed and validated on 77 peach cultivars, and nine accessions from two F2 populations, with 96 and 74% accuracy in determining expected CR genotype (compared to SNP array) and predicting phenotype, respectively. Furthermore, the Ppe.CR.1 showed 80% accuracy in predicting the precise CR phenotype in the Clemson University peach breeding material. Only one Ppe.CR.1 KASP assay (Ppe.CR.1-1) is needed to distinguish between haplotypes with CR lower and higher than 800 chilling hours, and two Ppe.CR.1 assays (Pp.CR.1-1 and -4), are capable of distinguishing low, moderate, and high CR alleles. Coupled with the crude DNA extraction, the Ppe.CR.1 DNA test provides a low-cost option for breeders and growers to predict CR in peach material with more than 70% accuracy.

Genome-Wide Identification, Evolution, and Expression Analysis of GASA Gene Family in Prunus mume.

The Gibberellic Acid Stimulated Arabidopsis/Gibberellin Stimulated Transcript (GASA/GAST) gene family is a group of plant-specific genes encoding cysteine-rich peptides essential to plant growth, development, and stress responses. Although GASA family genes have been identified in various plant species, their functional roles in Prunus mume are still unknown. In this study, a total of 16 PmGASA genes were identified via a genome-wide scan in Prunus mume and were grouped into three major gene clades based on the phylogenetic tree. All PmGASA proteins possessed the conserved GASA domain, consisting of 12-cysteine residues, but varied slightly in protein physiochemical properties and motif composition. With evolutionary analysis, we observed that duplications and purifying selection are major forces driving PmGASA family gene evolution. By analyzing PmGASA promoters, we detected a number of hormonal-response related cis-elements and constructed a putative transcriptional regulatory network for PmGASAs. To further understand the functional role of PmGASA genes, we analyzed the expression patterns of PmGASAs across different organs and during various biological processes. The expression analysis revealed the functional implication of PmGASA gene members in gibberellic acid-, abscisic acid-, and auxin-signaling, and during the progression of floral bud break in P. mume. To summarize, these findings provide a comprehensive understanding of GASA family genes in P. mume and offer a theoretical basis for future research on the functional characterization of GASA genes in other woody perennials.

Integrated transcriptome and small RNA sequencing in revealing miRNA-mediated regulatory network of floral bud break in Prunus mume.

MicroRNAs is one class of small non-coding RNAs that play important roles in plant growth and development. Though miRNAs and their target genes have been widely studied in many plant species, their functional roles in floral bud break and dormancy release in woody perennials is still unclear. In this study, we applied transcriptome and small RNA sequencing together to systematically explore the transcriptional and post-transcriptional regulation of floral bud break in P. mume. Through expression profiling, we identified a few candidate genes and miRNAs during different developmental stage transitions. In total, we characterized 1,553 DEGs associated with endodormancy release and 2,084 DEGs associated with bud flush. Additionally, we identified 48 known miRNAs and 53 novel miRNAs targeting genes enriched in biological processes such as floral organ morphogenesis and hormone signaling transudation. We further validated the regulatory relationship between differentially expressed miRNAs and their target genes combining computational prediction, degradome sequencing, and expression pattern analysis. Finally, we integrated weighted gene co-expression analysis and constructed miRNA-mRNA regulatory networks mediating floral bud flushing competency. In general, our study revealed the miRNA-mediated networks in modulating floral bud break in P. mume. The findings will contribute to the comprehensive understanding of miRNA-mediated regulatory mechanism governing floral bud break and dormancy cycling in wood perennials.

The Impact of Dormancy Breakers on Hormone Profiles, Fruit Growth and Quality in Sweet Cherry

Chemical dormancy breakers are often used to manipulate floral bud break in sweet cherry production, and their use is increasing due to unpredictable climate effects. The role of plant hormones in regulating the critical transition of floral buds from dormant to opening in deciduous trees is now emerging. By monitoring changes in endogenous hormone levels within floral buds that are undergoing the transition from dormant to the growing state in response to various cues (environmental and/or chemical inducers), we can begin to distinguish the plant hormones that are the drivers of this process. This study sought to identify key hormonal regulators of floral bud break using sweet cherry as a model and modifying timing of bud break through the application of two chemical dormancy breakers, hydrogen cyanamide (HC, Dormex®) and emulsified vegetable oil compound (EVOC, Waiken®), and to determine the effect of these chemicals on fruit growth and quality. Treatments were applied at label rates 35–40 days before estimated bud break. We found that HC-treated tree buds broke earlier, and this was associated with a significant early elevation of the cytokinins dihydrozeatin and dihydrozeatin riboside compared to the control and EVOC-treated tree buds. In contrast, changes in auxin and abscisic acid content did not appear to explain the hastened bud burst induced by hydrogen cyanamide. While HC-treated trees resulted in larger fruit, there was a higher incidence of cracked fruit and the pack-out of A-grade fruit was reduced. The increase in fruit size was attributed to the earlier flowering and hence longer growing period. Harvest assessment of fruit quality showed no treatment effect on most quality parameters, including fruit dry matter content, total soluble solids or malic acid content, but a reduction in fruit compression firmness and stem pull force in EVOC-treated trees was observed. However, all fruit still met the Australian industry fruit quality export market standards. This study offers important insights into bud hormonal activities underpinning the action of these chemical regulators; understanding bud responses is critically important to ensuring consistent and sustainable fruit tree production systems into the future. It also demonstrates that the dormancy-breaking agents HC and EVOC have no detrimental impact on fruit quality at harvest or following storage, however growers need to be aware of the potential for increased fruit cracking when earlier bud break results in a longer growing season which has the potential to increase fruit size. Further studies are required to determine the role of gibberellin in hastening bud break by dormancy breakers.

Peach [Prunus persica (L.) Batsch] Cultivars Differ in Apparent Base Temperature and Growing Degree Hour Requirement for Floral Bud Break.

Bud break timing in peach [Prunus persica (L.) Batsch] is determined by the sequential fulfillment of a chilling requirement (CR) and a heat requirement (HR) for development. Genotypic variation in CR has been well characterized in peach. Adapting peaches to low chilling environment through reduced CR can make them susceptible to crop destroying spring frosts, if bloom occurs too early. Potential variation in HR between accessions has received less attention due to the methodological difficulty in assessing HR independently of CR. HR could vary in the magnitude of growing degree hours (GDHs) and/or the base temperature at which GDH accumulation begins. Characterizing HR traits in peach accessions could allow improved bloom time modeling and selection of phenotypes with improved spring frost avoidance through delayed bloom. We estimated GDH and apparent base temperature for floral bud break by observing time to floral bud break at several constant forcing temperatures. We evaluated 54 peach accessions (representing a range of CR) in which chilling had been saturated after >1,700 h at 3°C. Accessions differed widely in both the GDH requirement (2,015 to 11,191°C⋅h) and apparent base temperature (−1.85 to 8.69°C) for GDH accumulation. GDH and apparent base temperature were negatively correlated. A simulation exercise was performed to assess relative importance of varying base temperature vs. GDH for delaying bloom at different chilling accumulations at three locations in the southeastern United States using 30 years of historical weather data. The aim of this study was to determine whether there may be unrecognized diversity in peach germplasm for two HR traits (base temperature and thermal time) to enable breeding efforts to delay floral bud break and reduce the frost exposure risk of developing flowers and fruits. Our results suggest that selecting cultivars for increased GDH would be a safer, more reliable strategy for delaying bloom than increasing base temperature for GDH accumulation.

Integrating Genome-Wide Association Analysis With Transcriptome Sequencing to Identify Candidate Genes Related to Blooming Time in Prunus mume.

Prunus mume is one of the most important woody perennials for edible and ornamental use. Despite a substantial variation in the flowering phenology among the P. mume germplasm resources, the genetic control for flowering time remains to be elucidated. In this study, we examined five blooming time-related traits of 235 P. mume landraces for 2 years. Based on the phenotypic data, we performed genome-wide association studies, which included a combination of marker- and gene-based association tests, and identified 1,445 candidate genes that are consistently linked with flowering time across multiple years. Furthermore, we assessed the global transcriptome change of floral buds from the two P. mume cultivars exhibiting contrasting bloom dates and detected 617 associated genes that were differentially expressed during the flowering process. By integrating a co-expression network analysis, we screened out 191 gene candidates of conserved transcriptional pattern during blooming across cultivars. Finally, we validated the temporal expression profiles of these candidates and highlighted their putative roles in regulating floral bud break and blooming time in P. mume. Our findings are important to expand the understanding of flowering time control in woody perennials and will boost the molecular breeding of novel varieties in P. mume.

Exogenous Gibberellic Acid and Cytokinin Effects on Budbreak, Flowering, and Yield of Blackberry Grown under Subtropical Climatic Conditions

In subtropical climates, inadequate winter chill limits blackberry (Rubus L. subgenus Rubus Watson) production by causing poor and erratic floral budbreak. To compensate for a lack of chilling, bud dormancy-breaking agents must be developed for subtropical blackberry production. Our previous study showed that gibberellic acid (GA3) promotes budbreak in three blackberry cultivars but has potential negative side effects on floral development in ‘Natchez’. 6-benzyladenine (6-BA) is a synthetic cytokinin that can act as an antagonist of gibberellins during floral transition. The objectives of this study were to evaluate cultivar × exogenous GA3 interactions, characterize dose effects of exogenous GA3, and examine synergistic effects of GA3 and 6-BA. Three field experiments were conducted in west central Florida. All spray treatments were applied at the end of the chilling period. In the first experiment, ‘Natchez’, ‘Navaho’, and ‘Ouachita’ were treated with GA3 at 0 or 99 g·ha−1. Budbreak was promoted by exogenous GA3 in all three cultivars (0.9% to 4.5% vs. 42.9% to 69.4%), but yield responses varied considerably. Exogenous GA3 increased the yield of ‘Navaho’ and ‘Ouachita’ by 560% to 931%, whereas it induced flower abortion and caused a 15% yield reduction in ‘Natchez’. In the second experiment, ‘Natchez’ was treated with GA3 at 0, 25, 99, or 198 g·ha−1. Budbreak increased linearly with GA3, but yield decreased exponentially with GA3 because of dose-dependent flower abortion. In the third experiment, ‘Natchez’ was subjected to five treatments: 1) water control; 2) GA3 spray application; 3) 6-BA spray application; 4) combined spray application of GA3 and 6-BA; and 5) sequential spray application of 6-BA at 9 days after GA3 application. Application rates were 99 and 47 g·ha−1 for GA3 and 6-BA, respectively. Exogenous 6-BA suppressed GA3-induced flower abortion only to a limited extent. As a result, GA3-containing treatments caused 65% to 83% yield reductions compared with the control (2382 vs. 410–823 g/plant). These results demonstrate that GA3 is a highly effective bud dormancy-breaking agent for blackberry. However, the drawback of GA3 is cultivar-dependent flower abortion, which cannot be fully mitigated by 6-BA. The use of GA3 can be an important management practice for subtropical blackberry production, but its practical implementation must consider cultivar-dependent responses.

The chromosome-level wintersweet (Chimonanthus praecox) genome provides insights into floral scent biosynthesis and flowering in winter

BackgroundWintersweet (Chimonanthus praecox), an important ornamental plant, has evolved unique fragrant aroma and winter-flowering properties, which are critical for its successful sexual reproduction. However, the molecular mechanisms underlying these traits are largely unknown in this species. In addition, wintersweet is also a typical representative species of the magnoliids, where the phylogenetic position of which relative to eudicots and monocots has not been conclusively resolved.ResultsHere, we present a chromosome-level wintersweet genome assembly with a total size of 695.36 Mb and a draft genome assembly of Calycanthus chinensis. Phylogenetic analyses of 17 representative angiosperm genomes suggest that Magnoliids and eudicots are sister to monocots. Whole-genome duplication signatures reveal two major duplication events in the evolutionary history of the wintersweet genome, with an ancient one shared by Laurales, and a more recent one shared by the Calycantaceae. Whole-genome duplication and tandem duplication events have significant impacts on copy numbers of genes related to terpene and benzenoid/phenylpropanoid (the main floral scent volatiles) biosynthesis, which may contribute to the characteristic aroma formation. An integrative analysis combining cytology with genomic and transcriptomic data reveals biological characteristics of wintersweet, such as floral transition in spring, floral organ specification, low temperature-mediated floral bud break, early blooming in winter, and strong cold tolerance.ConclusionsThese findings provide insights into the evolutionary history of wintersweet and the relationships among the Magnoliids, monocots, and eudicots; the molecular basis underlying floral scent biosynthesis; and winter flowering, and highlight the utility of multi-omics data in deciphering important ornamental traits in wintersweet.

Response of potting media composition for pot mum chrysanthemum production (Dendranthema grandiflora L.)

An investigation was carried out with ten potting media for pot mum chrysanthemum production at Department of Horticulture, RCA Campus, MPUAT, Udaipur during 2016-2017 to find out suitable potting media combination for growth, floral and media analysis parameter. The experiment was laid out in Completely Randomized Design with 20 replications and 10 potting media as treatment. The data were analyzed by analysis of variance technique at 5% level of significance. The maximum value for plant height (20.45cm), plant spread (15.69cm), intermodal length (3.29, 4.54cm at 30,60 DAT), stem diameter (4.43mm), branches plant-1 (7.15), days to, flower diameter (1.91cm), spray plant-1 (7.60), days to flower withering (149.45). flower plant-1(50.60), flower weight (46.54gm.), flower durations (45.95days), pH (6.1), EC (0.64dsm-1), water holding capacity (87.85%) of potting media before transplanting, pH, EC, water holding capacity (7.3), (1.47 ds/m) and (97.36%) respectively after completion of flowering phase and percent plant survival (96.70), while earliest first flower bud appearance (75.30 days), bud show color (83 days), floral bud break (101.50 days) were recorded in potting media treatment combination consisting from Soil : Sand : FYM : Vermicompost (2:1:0.5:0.5 v/v). On the basis of result obtained it is concluded that potting media treatment combination consisting from Soil : Sand : FYM : Vermicompost (2:1:0.5:0.5 v/v) were found best for pot mum chrysanthemum production over treatments.

A High Resolution Melting Analysis-Based Genotyping Toolkit for the Peach (Prunus persica) Chilling Requirement.

The chilling requirement (CR) is the main factor controlling the peach floral bud break and subsequent reproductive growth. To date, several peach CR quantitative trait loci (QTLs) have been identified. To improve the accessibility and convenience of this genetic information for peach breeders, the aim of this study was to establish an easy-to-use genotype screening system using peach CR molecular markers as a toolkit for marker-assisted selection. Here, we integrated 22 CR-associated markers from three published QTLs and positioned them on the Prunus persica physical map. Then, we built a PCR-based genotyping platform by using high-resolution melting (HRM) analysis with specific primers and trained this platform with 27 peach cultivars. Due to ambiguous variant calls from a commercial HRM software, we developed an R-based pipeline using principal component analysis (PCA) to accurately differentiate genotypes. Based on the PCA results, this toolkit was able to determine the genotypes at the CR-related single nucleotide polymorphisms (SNPs) in all tested peach cultivars. In this study, we showed that this HRM-PCA pipeline served as a low-cost, high-throughput, and non-gel genotyping solution. This system has great potential to accelerate CR-focused peach breeding.

Response of “White Robin” Peach Trees Cv. (Prunus persica L.) to Cultivation Under Plastic Covering Conditions and Foliar Application by Hydrogen Cyanamide and Garlic Extract

A field experiment was carried out during 2018 and 2019 seasons on 4 years old ‘White Robin’ peach trees cv. (Prunus persica L.), to investigate the effect of cultivation peach trees under plastic covering conditions (PC) with combination of hydrogen cyanamide (HC at 0.5%) as a Dormex and garlic extract (GE at 1%) on floral and vegetative bud break time, vegetative growth parameters, fruit set, yield and fruit quality of this cultivar. Eight treatments, HC alone, GE alone, HC + GE, PC alone, PC + HC, PC + GE, PC + HC + GE and control were applied. The application of HC and GE under PC, resulted in earlier buds break and harvesting period by 10 and 20 days, respectively. Moreover, it shortened the period between both of flower and vegetative buds break and onset to end fruit harvesting by 10 days. It significantly increased shoot length, diameter and leaf area compared to control and other treatments. Furthermore, it improved fruit physical and chemical properties beside increasing the yield by 30%. All studied parameters gradually improved by other investigated treatments as follow: PC + HC, PC + GE, PC alone, HC and GE, HC alone then GE alone compared by control. Plastic covering might be useful for early peach cultivars for advancing fruit maturity and improving yield and fruit quality, that will be more suitable for exportation and profitable for growers under conditions of Egypt.

Effect of a Late Spring Application of Hydrogen Cyanamide on High-Chill Peaches

Due to a record low chilling accumulation in the winter of 2016–2017, many high-chill peach cultivars displayed almost no budbreak by mid-April of 2017 in central Georgia, USA, where budbreak usually occurs around mid-March. In this study, nine of these peach cultivars were used to study the effect of a late spring Dormex spray application (April 13, 2017) on subsequent budbreak, year-end cumulative vegetative growth, and following-season yield. Dormex was found to have strong stimulating effects on lateral budbreak, but little effect on terminal and floral budbreak. It also had apparent phytotoxic effects on lateral, terminal and floral buds, and growth. The effects varied among genotypes, tree ages, and shoot types. The peak of the effects occurred two weeks post-application. Most floral buds abscised before they swelled. Between Dormex-sprayed trees and unsprayed controls, there was no significant difference in the number and average length of the new lateral shoots by the end of 2017, nor in the number and weight of the fruit harvested in 2018. In conclusion, our data showed a late spring Dormex spray application stimulated earlier lateral budbreak and caused some level of phytotoxicity to all types of buds and new growth, but had little impact on flower budbreak, fruit set, year-end vegetative growth, or following-season yield. These findings provide useful information for growers, considering the need for spraying dormancy-breaking compounds when faced with insufficient chilling.

Controlled-temperature Treatments with Low-cost, Off-the-shelf Equipment for Bud or Seed Forcing Experiments

Inexpensive plug-and-play temperature controllers have recently become available. These allow a chest freezer to be programmed easily to hold a desired set point across a range of biologically relevant temperatures. Installation can be completed in a few minutes using consumer-grade chest freezers. We used these temperature controllers to create five temperature-controlled chambers at 12, 14, 16, 18, and 20 °C. We demonstrated the use of these controlled-temperature chambers with two biologic assays: floral budbreak of peach [Prunus persica (L.) Batsch] stem cuttings and germination of sunflower (Helianthus annuus L.) seeds. We used the budbreak and germination rates at multiple temperatures to estimate base temperatures and thermal time requirements for development.

Performance of an elite, hybrid family of a northern × southern highbush cross (‘Draper’ × ‘Jewel’)

A family of the cross of the northern highbush blueberry ‘Draper’ × the southern highbush ‘Jewel’ (D × J) was propagated and phenotyped for plant size, yield, rate of flower, bud, and fruit development, leafing ability, winter hardiness, and fruit quality for 2 years in the field in Florida (FL), Georgia (GA), Michigan (MI), and Oregon (OR). In addition, a controlled greenhouse study was conducted on these progenies to estimate their chilling requirements. Significant levels of genotypic variability were observed for all the traits and the majority showed significant location and genotype × environmental interactions. Most of these traits were normally distributed across genotypes. There were many more flower buds per cane in GA than FL and OR, and many more vegetative buds broke in OR than in the southeastern states. Most of the various yield and growth traits were significantly correlated, except for flower buds per cane with plant height and width, and strength of leafing with plant width and flower buds/cane. Plants in OR developed much more slowly than those in FL and GA. There was a significant G × E effect on days to early green tip, floral bud break, and full bloom. Significant correlations were observed between all the developmental rates except between floral bud break and the days to full flowering and first blue fruit. Most individuals were severely damaged by winter cold in MI, although a few showed good tolerance. Significant location effects were observed for pH, titratable acidity (TA), soluble solids (SS), and SS/TA. Fruit in FL were a little softer and had higher SS/TA ratios than those in GA. There were significant interactions between genotype and environment for all the fruit quality traits except for fruit scar, firmness, anthocyanin content (ACY), and % juice. Fruit scar had a significant positive relationship with firmness and a significant negative relationship with flavor. Fruit color was significantly associated positively with soluble solids and ACY. Firmer fruit had significantly lower levels of ACYs. Fruit pH showed significant positive correlations with TA, TA/SS, and % juice, and significant negative relationship with SS and ACY. TA was significantly associated negatively with TA/SS and positively with ACY and % juice. TA/SS and ACY were positively correlated significantly with % juice. Two or three individuals were identified at each location that had high yields, were very early or late ripening and had excellent overall fruit quality. There were significant levels of genotypic, environmental (chilling hours) and G × E interaction among vegetative and floral buds for numbers of buds per shoot, percentage that developed and their developmental rate. The chilling requirement of highbush blueberry appears to be regulated polygenically as the D × J family segregated normally. On average, genotypes did more poorly at 250 and 350 chilling hours than the other chilling treatments.

Absorption, distribution and accumulation of nitrogen applied at different phenological stages in southern highbush blueberry ( Vaccinium corymbosum interspecific hybrid)

Abstract Southern highbush blueberry has an early harvesting and then a long period of vegetative growth until dormancy, compared to highbush and rabbiteye blueberries. Nitrogen requirements could be different because of this specific early harvesting. Absorption of 15N enriched ammonium sulfate was compared at five phenological stages from bud swell to pre-dormancy in two years old plants of the cultivars Star and ONeal. Plants grown in pots were irrigated with ammonium sulfate solution (15N). Five plants for each application date were excavated and separated in parts (roots, canes, leaves, flowers, fruits or floral buds). Samples were taken three weeks after application from bud swell to pre-harvest treatment, and three month after for post-harvest and pre-dormancy treatment. Each tissue were dried and weighed before and after, and analyzed for 15N content, N content and N %....N%, and in leaves were also determined macro and micro nutrients. Nitrogen fertilization at bud swell is effective, even for the ONeal cultivarthat present floral bud break in absence of leaves. Post-harvest fertilization contribute N for summer vegetativegrowth which would influence the floral buds development next year, Nitrogenstorage at this time would led to the improved floral behavior next year. Nitrogen losses risk is lower at post-harvestfertilization.