scholarly journals Daylength, Cold Storage, and Plant-production Method Influence Growth and Flowering of Asclepias tuberosa

HortScience ◽  
1991 ◽  
Vol 26 (2) ◽  
pp. 120-121 ◽  
Author(s):  
Mary Lewnes Albrecht ◽  
Jerald T. Lehmann
Keyword(s):  
Cold Storage ◽  
Storage Temperature ◽  
Production Method ◽  
Flowering Plants ◽  
Plant Production ◽  
Flower Buds ◽  
Planting Depth ◽  
Production Scheme ◽  
Post Production ◽  
Delayed Flowering

Greenhouse- and field-produced plants of Asclepias tuberosa L., butterfly flower, were forced in the greenhouse under various daylengths to produce flowering plants for the florist industry. Examined were post-production cold storage temperature (4.5 and 10C) and period (12, 14, and 16 weeks), forcing daylength (9, 13, 15, or 17 hours), plant-production scheme (greenhouse- vs. field-produced), and planting depth (exposed crowns or crowns planted 1.3 cm below the medium surface). When forced under a 9-hour daylength, blind shoots and aborted flower buds were prevalent. When daylengths exceeded 13 hours, using night interruption, the time to produce a marketable plant was reduced from 71 days to 61 days for 18-month-old greenhouse-produced plants. Daylength of 17 hours delayed flowering of field-produced liners by 15 days in comparison to those forced under 13-hour daylength. Greenhouse-produced plants stored at 10C did not sprout when brought into the forcing greenhouse held at 17/25C (night/day). Field-produced plants, when greenhouse-forced, had fewer flowers per inflorescence (88 to 94 flowers) than greenhouse-produced plants (79 to 87 flowers).

scholarly journals Florigen governs shoot regeneration

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yaarit Kutsher ◽  
Michal Fisler ◽  
Adi Faigenboim ◽  
Moshe Reuveni
Keyword(s):  
Nitric Oxide ◽  
Shoot Regeneration ◽  
Ectopic Expression ◽  
Flowering Plants ◽  
Regeneration Capacity ◽  
No Donor ◽  
Tobacco Leaves ◽  
Age Related ◽  
Delayed Flowering

AbstractIt is widely known that during the reproductive stage (flowering), plants do not root well. Most protocols of shoot regeneration in plants utilize juvenile tissue. Adding these two realities together encouraged us to study the role of florigen in shoot regeneration. Mature tobacco tissue that expresses the endogenous tobacco florigen mRNA regenerates poorly, while juvenile tissue that does not express the florigen regenerates shoots well. Inhibition of Nitric Oxide (NO) synthesis reduced shoot regeneration as well as promoted flowering and increased tobacco florigen level. In contrast, the addition of NO (by way of NO donor) to the tissue increased regeneration, delayed flowering, reduced tobacco florigen mRNA. Ectopic expression of florigen genes in tobacco or tomato decreased regeneration capacity significantly. Overexpression pear PcFT2 gene increased regeneration capacity. During regeneration, florigen mRNA was not changed. We conclude that florigen presence in mature tobacco leaves reduces roots and shoots regeneration and is the possible reason for the age-related decrease in regeneration capacity.

scholarly journals Pengaruh Perlakuan Waktu dan Suhu Penyimpanan Dingin terhadap Mutu Kubis Bunga (Brassica Oleracea Var. Botrytis L.)

2019 ◽  
Vol 8 (1) ◽  
pp. 138
Author(s):  
Chyntia Wulandari Eka Saputri ◽  
I. A. Rina Pratiwi Pudja ◽  
Pande Ketut Diah Kencana
Keyword(s):  
Weight Loss ◽  
Shelf Life ◽  
Cold Storage ◽  
Storage Time ◽  
Consumption Rate ◽  
Storage Temperature ◽  
Treatment Time ◽  
O2 Consumption ◽  
Damage Level ◽  
Four Levels

Tujuan dari penelitian ini adalah untuk menentukan waktu perlakuan optimal dan suhu penyimpanan dingin untuk mutu kubis bunga. Penelitian ini menggunakan rancangan acak lengkap (RAL) yang terdiri dari dua faktor, faktor pertama adalah suhu yang digunakan dan faktor kedua adalah waktu selama show case. Faktor pertama terdiri dari dua level, yaitu (P1): show case temperature 8oC, dan (P2): show case temperature 15oC dan tambah kontrol (P0). Faktor kedua terdiri dari empat level, yaitu (A0): penyimpanan selama 0 jam, (A1): penyimpanan selama 12 jam, (A2): penyimpanan selama 16 jam, (A3): penyimpanan selama 20 jam dan diulang untuk 3 kali ulangan. Kubis bunga sebagai kontrol disimpan pada suhu kamar (28 ± 1 ?). Parameter kualitas yang diamati dalam penelitian ini termasuk penurunan berat badan, tingkat konsumsi O2, warna (warna berbeda), uji organoleptik termasuk umur simpan dan tingkat kerusakan. Hasil penelitian menunjukkan parameter penurunan susut bobot, laju konsumsi O2, warna, umur simpan, tingkat kerusakan pada suhu perlakuan suhu terbaik adalah suhu 8 ? dan waktu penyimpanan 20 jam (P1A3).Kata kunci: kembang kol, waktu penyimpanan, suhu penyimpanan dingin   The purpose of this study was to determine the optimal treatment time and cold storage temperature for the quality of cabbage flowers. This study uses a completely randomized design (CRD) consisting of two factors, the first factor is the temperature used and the second factor is the time during the showcase. The first factor consists of two levels, namely (P1): showcase temperature of 8oC, and (P2): showcase temperature of 15oC and added a control (P0). The second factor consists of four levels, namely (A0): storage for 0 hours, (A1): storage for 12 hours, (A2): storage for 16 hours, (A3): storage for 20 hours and repeated for 3 replications. Flower cabbage as control was stored at room temperature (28 ± 1 ?). The quality parameters observed in this study included weight loss, O2 consumption rate, color (color different), organoleptic tests including shelf life and damage level. The results showed the parameters of weight loss, O2 consumption rate, color, shelf life, damage rate at the best temperature of 8 ? and storage time of 20 hours (P1A3). Keywords: cauliflower, storage time, cold storage temperature

Effects of Storage Temperature and Preservative Treatment on Shelf Life of the Pond-Raised Freshwater Fish, Silver Perch (Bidyanus bidyanus)

2001 ◽  
Vol 64 (10) ◽  
pp. 1584-1591 ◽  
Author(s):  
A. GELMAN ◽  
L. GLATMAN ◽  
V. DRABKIN ◽  
S. HARPAZ
Keyword(s):  
Shelf Life ◽  
Cold Storage ◽  
Storage Temperature ◽  
Storage Period ◽  
Potassium Sorbate ◽  
Test Results ◽  
Bacterial Composition ◽  
Fish Flesh ◽  
Microbiological Characteristics ◽  
Initial Load

Sensory and microbiological characteristics of pond-raised freshwater silver perch (Bidyanus bidyanus) fish, during cold storage over a period of 25 days were evaluated. Whole fish (averaging 400 g each) were stored in cold storage rooms at either 0 to 2°C, 5°C, or 5°C + potassium sorbate as a preservative. The organoleptic and hypoxanthine test results show that the treatment of potassium sorbate can slow the process of spoilage by about 5 days. Yet, the most important factor affecting the shelf life of these fish is the storage temperature. Keeping the fish at 0 to 2°C can prolong the storage prior to spoilage by 10 days compared with those kept at 5°C. These results obtained through organoleptic tests are corroborated by both the chemical (hypoxanthine and total volatile basic nitrogen) and to some extent by the physical (cosmos) tests. The initial total bacteriological counts were 5 × 102 CFU/cm2 for fish surface and <102 CFU/g for fish flesh, and these counts rose continuously, reaching about 106 CFU/g (0 to 2°C) and 107 CFU/g (5°C) in flesh and 107 to 108 CFU/cm2 on the surface by the end of the storage period. The addition of potassium sorbate led to a smaller increase in bacterial numbers, especially during the first 15 days. Bacterial composition fluctuated during storage. The initial load on the fish surface was predominantly mesophilic and gram positive and consisted mostly (80%) of Micrococci, Bacillus, and Corynebacterium. During the next 10 days, these bacteria were practically replaced by gram-negative flora comprised mostly of Pseudomonas fluorescens that rapidly increased with storage time and accounted for 95% after 15 days.

scholarly journals Evaluasi Penyimpanan Spermatozoa Ayam Pada Suhu 5⁰C, 26⁰C Dengan Pengencer Infuse NaCl, Glukosa 5% dan 10%

2021 ◽  
pp. 10-19
Author(s):  
Asnawi Asnawi ◽  
Maskur Maskur ◽  
Adji Santoso Dradjat
Keyword(s):  
Cold Storage ◽  
Room Temperature ◽  
Storage Temperature ◽  
Room Temperature Storage ◽  
C Storage ◽  
Better Than ◽  
Temperature Storage

The purpose of this study were to compare the quality of spermatozoa stored at 26⁰C, 5⁰C using diluents of NaCl, 10% glucose and 5% glucose. The spermatozoa of a rooster was collected and divided into 6 parts, each 2 tubes diluted in a ratio of 1:1 using NaCl, Glucose5% and Glucose 10%, then each 3 tubes with different diluents were stored at 26⁰C and 5⁰C. Observations of motility, viability and abnormalities of spermatozoa were carried out half an hour, 1 hour after dilution, followed every 2 hours until the ninth hours. The results showed that spermatozoa stored for 9 hours at a temperature of 26⁰C with a physiological diluent of NaCl, 10% Glucose and 5% Glucose each were different (P, < 0.05) with motility 50 ± 0.0%, 42 ± 10.95. % and 34±8.94%, respectively. At storage temperature of 5⁰C for 9 hours, physiological NaCl, 10% glucose and 5% glucose were significantly different (P<0.05) with motility 58.00±10.95%, 46.00±8.94% and 38.00±, respectively. 10.95% in a row. The viability of spermatozoa at 26⁰C storage with 5% glucose diluent was better than 10% glucose and physiological NaCl (P<0.05), 58.93±1.27%, 42.93±1.48% and 33.43±1.27% , while the physiological NaCl diluent and 10% glucose were not significantly different (P>0.05). At 5⁰C storage the viability of spermatozoa in the three diluents was not significantly different, with values of Glucose 10%, Glucose 5% and physiological NaCl 52.57±5.15%, 52.21±5.02% and 48.14±8.09%, respectively. Spermatozoa abnormalities at storage temperature 26⁰C and 5⁰C for 9 hours using physiological NaCl diluent, 5% glucose and 10% glucose, were not significantly different and varied between 5 to 10%. Finally, it can be concluded that at room temperature storage less than 4 hours the quality of spermatozoa was better with 5% glucose diluent, while for cold storage beyond 4 hours the quality of spermatozoa with NaCl diluent was higher

scholarly journals THE ASSOCIATION OF FLOWERING HABIT WITH WINTER SURVIVAL IN RED AND ALSIKE CLOVER DURING THE SEEDLING YEAR OF GROWTH

1960 ◽  
Vol 40 (2) ◽  
pp. 335-344 ◽  
Author(s):  
Henri P. Therrien ◽  
Dale Smith
Keyword(s):  
Red Clover ◽  
Dry Weight ◽  
Flowering Plants ◽  
Winter Survival ◽  
Lower Percentage ◽  
Flower Buds ◽  
Root Branching ◽  
Crown Root

The percentage of plants that flowered in the seedling year in spaced populations of red and alsike clovers at Madison and Arlington, Wisconsin, was highest in the earliest seedings (May 15) and decreased with later seeding dates. No plants flowered in the July 15th seedings. The percentage of winterkilling during the first winter was higher in the flowering plants of each clover than in the non-flowering plants. Differences in flowering and winter survival were noted among clover strains and in winter survival among plant types within strains.Prevention of flowering in medium red clover by removing flower buds, flowering stems and/or elongating tillers resulted in greater vegetative vigour and winter survival. Plants that were allowed to flower freely in the seedling year in spaced populations had a smaller number of non-flowering crown tillers, a smaller width of crown, a lower dry weight of crown, root and total available carbohydrates in the roots, less root branching, a slightly lower percentage of total available carbohydrates in the roots, and more winterkilling during the first winter than plants that were prevented from flowering. These responses may help in part to explain the benefits attributed to clipping red clover in the seedling year.

scholarly journals Gibberellin4+7, Benzyladenine, and Supplemental Light Improve Postharvest Leaf and Flower Quality of Cold-stored `Stargazer' Hybrid Lilies

1998 ◽  
Vol 123 (4) ◽  
pp. 563-568 ◽  
Author(s):  
Anil P. Ranwala ◽  
William B. Miller
Keyword(s):  
Cold Storage ◽  
Storage Temperature ◽  
Postharvest Quality ◽  
Flower Longevity ◽  
Flower Bud ◽  
Leaf Injury ◽  
Leaf Chlorosis ◽  
Bud Opening ◽  
Flower Quality

Experiments were conducted to evaluate storage temperature, storage irradiance and prestorage foliar sprays of gibberellin, cytokinin or both on postharvest quality of Oriental hybrid lilies (Lilium sp. `Stargazer'). Cold storage of puffy bud stage plants at 4, 7, or 10 °C in dark for 2 weeks induced leaf chlorosis within 4 days in a simulated consumer environment, and resulted in 60% leaf chlorosis and 40% leaf abscission by 20 days. Cold storage also reduced the duration to flower bud opening (days from the end of cold storage till the last flower bud opened), inflorescence and flower longevity, and increased flower bud abortion. Storage at 1 °C resulted in severe leaf injury and 100% bud abortion. Providing light up to 40 μmol·m-2·s-1 during cold storage at 4 °C significantly delayed leaf chlorosis and abscission and increased the duration of flower bud opening, inflorescence and flower longevity, and reduced bud abortion. Application of hormone sprays before cold storage affected leaf and flower quality. ProVide (100 mg·L-1 GA4+7) and Promalin (100 mg·L-1 each GA4+7 and benzyladenine (BA)) effectively prevented leaf chlorosis and abscission at 4 °C while ProGibb (100 mg·L-1 GA3) and ABG-3062 (100 mg·L-1 BA) did not. Accel (10 mg·L-1 GA4+7 and 100 mg·L-1 BA) showed intermediate effects on leaf chlorosis. Flower longevity was increased and bud abortion was prevented by all hormone formulations except ProGibb. The combination of light (40 μmol·m-2·s-1) and Promalin (100 mg·L-1 each GA4+7 and BA) completely prevented cold storage induced leaf chlorosis and abscission.

scholarly journals RcAP1, a Homolog of APETALA1, is Associated with Flower Bud Differentiation and Floral Organ Morphogenesis in Rosa chinensis

2019 ◽  
Vol 20 (14) ◽  
pp. 3557 ◽  
Author(s):  
Yu Han ◽  
Aoying Tang ◽  
Jiayao Yu ◽  
Tangren Cheng ◽  
Jia Wang ◽  
...  
Keyword(s):  
Floral Organ ◽  
Flower Buds ◽  
Flower Bud ◽  
Floral Organs ◽  
Rosa Chinensis ◽  
Organ Morphogenesis ◽  
Floral Primordia ◽  
Flower Bud Differentiation ◽  
Delayed Flowering

Rosa chinensis is one of the most popular flower plants worldwide. The recurrent flowering trait greatly enhances the ornamental value of roses, and is the result of the constant formation of new flower buds. Flower bud differentiation has always been a major topic of interest among researchers. The APETALA1 (AP1) MADS-box (Mcm1, Agamous, Deficiens and SRF) transcription factor-encoding gene is important for the formation of the floral meristem and floral organs. However, research on the rose AP1 gene has been limited. Thus, we isolated AP1 from Rosa chinensis ‘Old Blush’. An expression analysis revealed that RcAP1 was not expressed before the floral primordia formation stage in flower buds. The overexpression of RcAP1 in Arabidopsis thaliana resulted in an early-flowering phenotype. Additionally, the virus-induced down-regulation of RcAP1 expression delayed flowering in ‘Old Blush’. Moreover, RcAP1 was specifically expressed in the sepals of floral organs, while its expression was down-regulated in abnormal sepals and leaf-like organs. These observations suggest that RcAP1 may contribute to rose bud differentiation as well as floral organ morphogenesis, especially the sepals. These results may help for further characterization of the regulatory mechanisms of the recurrent flowering trait in rose.

scholarly journals Long-term hydrophilization of polydimethylsiloxane (PDMS) for capillary filling microfluidic chips

2019 ◽  
Vol 24 (1) ◽  
Author(s):  
Farzin Jahangiri ◽  
Tuuli Hakala ◽  
Ville Jokinen
Keyword(s):  
Cold Storage ◽  
Storage Temperature ◽  
Microfluidic Channel ◽  
Vibration Band ◽  
Microfluidic Chips ◽  
Thermally Activated ◽  
Capillary Filling ◽  
Different Temperatures ◽  
Long Term Preservation

AbstractWe present a simple and facile method for long-term preservation of hydrophilicity of oxygen plasma-hydrophilized poly (dimethylsiloxane) (PDMS) by cold storage. We show that storage under temperature of − 80 °C can maintain superhydrophilicity of plasma-exposed PDMS for at least 100 days. Storage at − 15 °C and at 22 °C room temperature (RT) is shown to exhibit, respectively, about half and full recovery of the original hydrophobicity after 100 days in storage. Furthermore, we investigated the implications of the cold storage for microfluidic applications, the capillary filling rate and the ability of the flow to bypass geometrical obstacles in a microfluidic channel. It is shown that the preservation of capillary filling properties of microchannels is in close agreement with the contact angle (CA) measurements and that the colder the storage temperature, the better the capillary filling capability of the channels is preserved. We ascribe the significantly reduced recovery rate to reduced thermally activated relaxation phenomena such as diminished diffusion of low molecular weight species (LMW) in the polymer matrix at colder temperatures. This is supported by ATR-FTIR measurements of the OH vibration band over time for samples stored at different temperatures.

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