Jojoba flower buds: effects of preconditioning temperature.

1982 ◽  
Vol 33 (4) ◽  
pp. 649 ◽  
Author(s):  
RL Dunstone
Keyword(s):  
Environmental Factors ◽  
Reproductive Cycle ◽  
Female Flower ◽  
Treatment Temperature ◽  
Bud Dormancy ◽  
Simmondsia Chinensis ◽  
Flower Buds ◽  
Flower Bud ◽  
Lower Treatment ◽  
Pretreatment Temperature

The environmental factors which control the reproductive cycle of jojoba (Simmondsia chinensis [Link] Schneider), were studied under controlled conditions. Plants were placed under a warm pretreatment temperature which resulted in the growth of new shoots bearing dormant flower buds. The plants were later moved to lower treatment temperatures which have been shown to break flower bud dormancy. Pretreatment temperature affected the percentage of nodes which produced flower buds. Both the pretreatment and the treatment temperature affected flowering percentage, there being an optimum pretreatment effect at 30/25�C day/night temperatures. Flowering percentage responded to absolute treatment temperature rather than to the drop in temperature from pretreatment to treatment. Flowering percentage increased with decrease in treatment temperature down to 15/10�C (male clone) and 12/7�C (female clone). The lowest pretreatment-treatment temperature combination was associated with the production of female flower parts on the male inflorescences.

scholarly journals The growth of flower bud, life history, and population structure of Rafflesia arnoldii (Rafflesiaceae) in Bengkulu, Sumatra, Indonesia

2020 ◽  
Vol 21 (2) ◽  
Author(s):  
AGUS SUSATYA
Keyword(s):  
Population Structure ◽  
Life History ◽  
Male Flower ◽  
Female Flower ◽  
Exponential Model ◽  
Flower Buds ◽  
Flower Bud ◽  
Dynamics Of Population ◽  
History Of ◽  
Two Populations

Abstract. Susatya A. 2020. The growth of flower bud, life history, and population structure of Rafflesia arnoldii (Rafflesiaceae) in Bengkulu, Sumatra, Indonesia. Biodiversitas 21: 792-798. The life history of Rafflesia arnoldii R.Br. is the reflection of the complex interaction between flower bud development and the external environments in order to reach its optimal survivorship. The objectives of the study were to determine the growth of flower buds at various development stages, to reconstruct the life history, and to know the population structure of R. arnoldii. The study was carried out at Taba Penanjung, Bengkulu Province, Indonesia. Two populations consisting of 17 individual buds of R. arnoldii were selected for the research. All buds were categorized into six visible stages, mapped, measured their diameters, and recorded their fates every two weeks for six months. The exponential model of growth development was applied to reconstruct the life history. The results showed that buds from the perigone stage respectively grew 3.5 and 12 times faster than those from the bract and cupule stages. The exponential growth of flower bud was confirmed, and explained by Y = 0.785 e0.0052 X, where Y and X were respectively diameter and age of flower bud. The complete life history of R. arnoldii required 3.5 to 5 years, where a female flower needed a longer time than a male flower. The population structure of R. arnoldii was not constant, but changed dynamically over time. The dynamics of population structure was mainly caused by the high mortality of small buds and the low flower bud recruitment.

THE EFFECTS OF PHOTOPERIOD, TEMPERATURE, AND LIGHT INTENSITY ON THE GROWTH OF THE LOWBUSH BLUEBERRY (VACCINIUM ANGUSTIFOLIUM AIT.)

1961 ◽  
Vol 39 (7) ◽  
pp. 1733-1739 ◽  
Author(s):  
I. V. Hall ◽  
R. A. Ludwig
Keyword(s):  
Environmental Factors ◽  
Vegetative Growth ◽  
Photoperiodic Response ◽  
Day Length ◽  
Flower Buds ◽  
Flower Bud ◽  
Bud Formation ◽  
Lowbush Blueberry ◽  
Flower Bud Formation ◽  
Field And Laboratory Conditions

A study of the effect of environmental factors on the growth and development of the lowbush blueberry was carried out using clonally propagated plants. In a preliminary study a definite photoperiodic response was found. Under 8-hour days flower buds were formed and no vegetative growth occurred. Under 16-hour days vegetative growth resulted and no flower bud formation occurred. In a replicated greenhouse experiment, seven clones produced flower buds with 8-, 10-, and 12-hour days, but produced none with 14- or 16-hour days. One clone produced flower buds with 8-, 10,- 12-, and 14-, but none with 16-hour days. Two clones were able to produce flower buds under all five photoperiods. Under 8- and 10- hour photoperiods no vegetative growth occurred. Under 12, 14, and 16 hours progressively more vegetative growth occurred. In an experiment on the interaction of temperature and photoperiod, vegetative growth was significantly greater at 70° F than at 50° F with the differences being accentuated by day length. Flower bud formation occurred with 11- and 13-hour photoperiods regardless of temperature, but was more pronounced at the higher temperatures. At 70° F, 15-hour photoperiod, no flower buds were formed while at 50° F, 15 hours, three clones produced no flower buds and six clones produced an abnormal type of inflorescence. Similar abnormal inflorescences were produced by giving plants 2, 3, or 4 weeks of 8-hour days. Six weeks of 8-hour days was sufficient to initiate normal inflorescences. Shade, provided by two layers of cheesecloth, significantly reduced the number of flower buds compared with full sunlight. The growth of the lowbush blueberry under field and laboratory conditions is discussed in relation to environmental factors.

scholarly journals Ethephon Prolongs Dormancy and Enhances Supercooling in Peach Flower Buds

1991 ◽  
Vol 116 (3) ◽  
pp. 500-506 ◽  
Author(s):  
Edward F. Durner ◽  
Thomas J. Gianfagna
Keyword(s):  
Prunus Persica ◽  
Storage Period ◽  
Bud Dormancy ◽  
Late Winter ◽  
Flower Buds ◽  
Flower Bud ◽  
Ethephon Treatment ◽  
Bud Growth ◽  
Peach Trees ◽  
Heat Requirement

The heat requirement for flower bud growth of container-grown peach trees [Prunus persica (L.) Batsch. cvs. Redhaven and Springold] in the greenhouse varied inversely and linearly with the length of the cold-storage period (SC) provided to break bud dormancy. Ethephon reduced the rest-breaking effectiveness of the 5C treatment. Buds from ethephon-treated trees grew more slowly than buds from untreated trees upon exposure to 20 to 25C, resulting in later bloom dates. The effect of ethephon on flower bud hardiness in field-grown trees of `Jerseydawn' and `Jerseyglo' was studied using exotherm analysis after deacclimation treatments. Bud deacclimation varied with reacclimating temperature (7 or 21 C), cultivar, ethephon treatment, and sampling date. All buds were more susceptible to injury in March than in January or February. Buds reacclimated more rapidly at 21C than at 7C. `Jerseyglo' reacclimated more rapidly than `Jerseydawn'. Untreated buds were less hardy and also reacclimated more rapidly than treated buds. Ethephon enhanced flower bud hardiness in three distinct ways: 1) it decreased the mean low-temperature exotherm of pistils, 2) it increased the number of buds that supercooled after exposure to reacclimating temperatures, and 3) it decreased the rate of deacclimation, especially at 21C. Ethephon prolongs flower bud dormancy by increasing the chilling requirement. The rate at which flower buds become increasingly sensitive to moderate temperatures in late winter and spring is thus reduced by ethephon. Thus, ethephon delays deacclimation during winter and delays bloom in the spring. Chemical name used: (2-chloroethyl) phosphoric acid (ethephon).

ENVIRONMENTAL FACTORS AFFECTING FLOWERING AND FRUIT DEVELOPMENT OF OPUNTIA FICUS-INDICA CUTTINGS DURING THE THREE WEEKS BEFORE PLANTING

1995 ◽  
Vol 43 (2) ◽  
pp. 151-157 ◽  
Author(s):  
Yitzchak Gutterman
Keyword(s):  
Environmental Factors ◽  
Fruit Development ◽  
Apical Part ◽  
Day Length ◽  
Flower Buds ◽  
Flower Bud ◽  
Opuntia Ficus Indica ◽  
Factors Affecting ◽  
Axillary Meristems ◽  
Lateral Branches

Opuntia ficus-indica(prickly pear) is a widespread desert perennial cactus shrub. The plants produce either lateral branches or flowers from the axillary meristems, depending on maternal and environmental influences.The flower buds develop from the axillary meristems mainly at the margin of the apical part of the terminal flat branch segments. Flower bud meristems start to be active and secrete mucus in January. The red-bracted flower buds start to appear in March/April, flowers open in May/June, and fruit matures in June/August.This study focused on the appearance of flower buds, flowers, and fruits after induction ofO. ficus-indicaone-segment branch cuttings by environmental factors during the 3-week healing period after cutting and before planting. The influence of treatments such as temperature, light intensity, and day length on flower bud appearance and fruit development is described.

scholarly journals Ethephon Treatment May Alleviate the Suppression of Female Flowers of Cucurbita Pepo under High Temperatures

HortScience ◽  
2006 ◽  
Vol 41 (6) ◽  
pp. 1421-1422 ◽  
Author(s):  
H.C. Wien
Keyword(s):  
High Temperature ◽  
High Temperatures ◽  
Elevated Temperatures ◽  
Female Flower ◽  
Flower Buds ◽  
Flower Bud ◽  
Ethylene Action ◽  
Ethephon Treatment ◽  
Flower Bud Formation ◽  
Female Flowers

When pumpkins are grown in elevated temperatures (32/27 °C day/night) for 1 week during flower development, fewer female flower buds are formed than at normal temperatures (20/15 °C) and only a small percentage of these reach anthesis. To determine if application of the ethylene-releasing compound ethephon can overcome the suppression of female flowers at high temperatures, `Baby Bear' pumpkin plants were sprayed at the two-leaf stage with 100 or 300 μL L–1 ethephon and then grown in hot and cool greenhouse compartments. At 20/15 °C, 17% of the first 15 main stem nodes produced female flower buds on control plants and virtually all of these developed into open flowers. The higher rate of ethephon increased female bud percentage to 37%. At 32/27 °C, only 3% of the nodes formed female flower buds and 2% flowered. Application of ethephon did not significantly increase female expression at high temperature, and none of the buds reached anthesis. Treatment with the inhibitor of ethylene action silver thiosulfate reduced female flower bud formation at the low temperature and entirely suppressed female flower buds at high temperature. In two additional experiments, these treatments were applied to two cultivars grown at a less extreme 32/20 and at 20/15 °C. Female buds and open flowers were moderately increased by ethephon in the high temperatures, suggesting that ethephon might foster female flowering in less extreme temperatures. Further work is needed to determine if ethephon treatment can overcome the heat-induced inhibition of female flowers in pumpkin under field conditions.

Cyclamen Leaf Unfolding Rate in Response to Temperature

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 447d-447
Author(s):  
Meriam Karlsson ◽  
Jeffrey Werner
Keyword(s):  
Day Length ◽  
Leaf Number ◽  
Cyclamen Persicum ◽  
Flower Buds ◽  
Flower Bud ◽  
Leaf Unfolding ◽  
Significant Difference ◽  
Number Of Leaves ◽  
Growth Chambers ◽  
Response To Temperature

Nine-week-old plants of Cyclamen persicum `Miracle Salmon' were transplanted into 10-cm pots and placed in growth chambers at 8, 12, 16, 20, or 24 °C. The irradiance was 10 mol/day per m2 during a 16-h day length. After 8 weeks, the temperature was changed to 16 °C for all plants. Expanded leaves (1 cm or larger) were counted at weekly intervals for each plant. The rate of leaf unfolding increased with temperature to 20 °C. The fastest rate at 20 °C was 0.34 ± 0.05 leaf/day. Flower buds were visible 55 ± 7 days from start of temperature treatments (118 days from seeding) for the plants grown at 12, 16, or 20 °C. Flower buds appeared 60 ± 6.9 days from initiation of treatments for plants grown at 24 °C and 93 ± 8.9 days for cyclamens grown at 8 °C. Although there was no significant difference in rate of flower bud appearance for cyclamens grown at 12, 16, or 20 °C, the number of leaves, flowers, and flower buds varied significantly among all temperature treatments. Leaf number at flowering increased from 38 ± 4.7 for plants at 12 °C to 77 ± 8.3 at 24 °C. Flowers and flower buds increased from 18 ± 2.9 to 52 ± 11.0 as temperature increased from 12 to 24 °C. Plants grown at 8 °C had on average 6 ± 2 visible flower buds, but no open flowers at termination of the study (128 days from start of treatments).

scholarly journals Regulation of Flowering Timing by ABA-NnSnRK1 Signaling Pathway in Lotus

2021 ◽  
Vol 22 (8) ◽  
pp. 3932
Author(s):  
Jing Cao ◽  
Qijiang Jin ◽  
Jiaying Kuang ◽  
Yanjie Wang ◽  
Yingchun Xu
Keyword(s):  
Protein Kinase ◽  
Environmental Changes ◽  
Molecular Genetic ◽  
Maximal Response ◽  
Protein Kinase Activity ◽  
Hormonal Changes ◽  
Flower Buds ◽  
Flower Bud ◽  
Aba Content ◽  
Flower Bud Abortion

The lotus produces flower buds at each node, yet most of them are aborted because of unfavorable environmental changes and the mechanism remains unclear. In this work, we proposed a potential novel pathway for ABA-mediated flower timing control in the lotus, which was explored by combining molecular, genetic, transcriptomic, biochemical, and pharmacologic approaches. We found that the aborting flower buds experienced extensive programmed cell death (PCD). The hormonal changes between the normal and aborting flower buds were dominated by abscisic acid (ABA). Seedlings treated with increasing concentrations of ABA exhibited a differential alleviating effect on flower bud abortion, with a maximal response at 80 μM. Transcriptome analysis further confirmed the changes of ABA content and the occurrence of PCD, and indicated the importance of PCD-related SNF1-related protein kinase 1 (NnSnRK1). The NnSnRK1-silenced lotus seedlings showed stronger flowering ability, with their flower:leaf ratio increased by 40%. When seedlings were treated with ABA, the expression level and protein kinase activity of NnSnRK1 significantly decreased. The phenotype of NnSnRK1-silenced seedlings could also be enhanced by ABA treatment and reversed by tungstate treatment. These results suggested that the decline of ABA content in lotus flower buds released its repression of NnSnRK1, which then initiated flower bud abortion.

Sign in / Sign up

Export Citation Format

Share Document