scholarly journals Effect of Temperature on Time to Flower of Coreopsis grandiflora, Chrysanthemum superbum, Gaillardia grandiflora, and Rudbeckia fulgida

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 861B-861 ◽  
Author(s):  
Mei Yuan ◽  
William H. Carlson ◽  
Royal D. Heins ◽  
Arthur C. Cameron

Scheduling crops to flower for specific dates requires a knowledge of the relationship between temperature and time to flower. Our objective was to determine the relationship between temperature and time to flower of four herbaceous perennials. Field-grown, bare-root Coreopsis grandiflora `Sunray', Gaillardia grandiflora `Goblin', Rudbeckia fulgida `Goldsturm', and tissue culture-propagated Chrysanthemum superbum `Snow Cap' were exposed to 5C for 10 weeks. They were grown at 15, 18, 21, 24 or 27C under 4-h night interruption lighting. Time to visible bud (VB) and first flower (FLW) were recorded. Days to VB, days to FLW, and days from VB to FLW decreased as temperature increased. Time to flower at 15C was 70, 64, 96, and 54 days and 24, 39, 48, and 36 days at 27C for Coreopsis, Gaillardia, Rudbeckia, and Chrysanthemum, respectively. The 27C temperature apparently caused devernalization on Coreopsis because only 40% of the plants flowered. The effects of temperature on flower size, flower bud number, and plant height also are presented.

HortScience ◽  
1998 ◽  
Vol 33 (4) ◽  
pp. 663-667 ◽  
Author(s):  
Mei Yuan ◽  
William H. Carlson ◽  
Royal D. Heins ◽  
Arthur C. Cameron

Scheduling crops to flower on specific dates requires a knowledge of the relationship between temperature and time to flower. Our objective was to quantify the effect of temperature on time to flower and plant appearance of four herbaceous perennials. Field-grown, bare-root Coreopsis grandiflora (Hogg ex Sweet.) `Sunray', Gaillardia ×grandiflora (Van Houtte) `Goblin', and Rudbeckia fulgida (Ait.) `Goldsturm', and tissue culture—propagated Leucanthemum ×superbum (Bergman ex J. Ingram) `Snowcap' plants were exposed to 5 °C for 10 weeks and then grown in greenhouse sections set at 15, 18, 21, 24, or 27 °C under 4-hour night-interruption lighting until plants reached anthesis. Days to visible bud (VB), days to anthesis (FLW), and days from VB to FLW decreased as temperature increased. The rate of progress toward FLW increased linearly with temperature, and base temperatures and degree-days of each developmental stage were calculated. For Coreopsis, Leucanthemum, and Rudbeckia, flower size, flower-bud number, and plant height decreased as temperature increased from 15 to 26 °C.


2020 ◽  
Author(s):  
Lei Qin ◽  
Qiang Sun ◽  
Jiani Shao ◽  
Yang Chen ◽  
Xiaomei Zhang ◽  
...  

Abstract Background: The effects of temperature and humidity on the epidemic growth of coronavirus disease 2019 (COVID-19)remains unclear.Methods: Daily scatter plots between the epidemic growth rate (GR) and average temperature (AT) or average relative humidity (ARH) were presented with curve fitting through the “loess” method. The heterogeneity across days and provinces were calculated to assess the necessity of using a longitudinal model. Fixed effect models with polynomial terms were developed to quantify the relationship between variations in the GR and AT or ARH.Results: An increased AT dramatically reduced the GR when the AT was lower than −5°C, the GR was moderately reduced when the AT ranged from −5°C to 15°C, and the GR increased when the AT exceeded 15°C. An increasedARH increased theGR when the ARH was lower than 72% and reduced theGR when the ARH exceeded 72%.Conclusions: High temperatures and low humidity may reduce the GR of the COVID-19 epidemic. The temperature and humidity curves were not linearly associated with the COVID-19 GR.


1986 ◽  
Vol 61 (2) ◽  
pp. 660-665 ◽  
Author(s):  
S. S. Segal ◽  
J. A. Faulkner ◽  
T. P. White

Our purpose was to determine the effect of temperature on the fatigability of isolated soleus and extensor digitorum longus (EDL) muscles from rats during repeated isometric contractions. Muscles (70–90 mg) were studied at 20–40 degrees C in vitro. Fatigability was defined with respect to both the time and number of stimuli required to reach 50% of the force (P) developed at the onset of the fatigue test. Fatigue was studied during stimulation protocols of variable [force approximately 70% of maximum force (Po)] and constant frequency (28 Hz). Results for soleus and EDL muscles were qualitatively similar, but fatigue times were longer for soleus than for EDL muscles. During the variable-frequency protocol, development of approximately 70% of Po required an increase in stimulation frequency as temperature increased. During stimulation at these frequencies, fatigue time shortened as temperature increased. For both fatigue protocols, the relationship between temperature and the number of stimuli required to reach fatigue followed a bell-shaped curve, with maximum values at 25–30 degrees C. The temperature optimum for maximizing the number of isometric contractions to reach fatigue reflects direct effects of temperature on muscle function.


2001 ◽  
Vol 19 (3) ◽  
pp. 140-144
Author(s):  
Gary J. Keever ◽  
J. Raymond Kessler ◽  
James C. Stephenson

Abstract A study was conducted to determine the effects of night-interrupted (NI) lighting initiated at different times in late winter on several herbaceous perennials produced outdoors in a southern nursery setting. Treatments were NI lighting beginning February 1, February 15, March 1, March 15, and a natural photoperiod. NI lighting accelerated flowering in ‘Goldsturm’ coneflower (Rudbeckia fulgida Ait. ‘Goldsturm’) 26–46 days in 1999 and 51–75 days in 2000, and in ‘Coronation Gold’ yarrow (Achillea x ‘Coronation Gold’) 2–9 days in 1999 and 2–11 days in 2000. Flower and flower bud counts increased 82–100% in ‘Coronation Gold’ achillea in 1999, 44–51% in ‘Butterfly Blue’ scabious (Scabiosa columbaria L. ‘Butterfly Blue’) and 100–151% in ‘Alaska’ shasta daisy (Leucanthemum x superbum Bergmans ex. J. Ingram ‘Alaska’) compared to counts of plants under natural photoperiod. With few exceptions, plant height increased under all NI lighting treatments, but in only ‘Goldsturm’ coneflower did it reduce plant quality. Clump verbena (Verbena canadensis L.) was minimally affected by NI lighting, and speedwell (Veronica spicata L. ‘Sunny Border Blue’) was not affected at all.


1949 ◽  
Vol 40 (2) ◽  
pp. 239-265 ◽  
Author(s):  
S. Pradhan

1. A series of exploratory experiments on the relationship between temperature and toxicity of DDT films to adults of Tribolium castaneum, and larvae of Plutella maculipennis, are described. The main conclusions with T. castaneum are:—(a) When the insects are continuously kept on the film at different temperatures there is a higher kill at higher temperatures.(b) When the insects are exposed to the film for about 24 hours at the same temperature and then kept away from it at different temperatures there is a higher kill at the lower temperature.(c) When the insects are kept on the film at different temperatures for about 24 hours and then kept away from the film for reaction at the same temperature, there is a higher kill in those kept on the film at the higher temperature.(a) and (b) above apply equally to larvae of P. maculipennis but (c) is reversed. The probable cause of this reversal appears to be the observed fact that at higher temperatures these larvae cover the film with much more silk thread and thus avoid contact to a greater extent than at lower temperatures.2. A review of literature, in the light of the conclusions arrived at, indicate that many of the observations made upon the temperature-toxicity relationship can be accounted for by the following generalisations:—(a) Insect resistance to poisons changes with temperature as do its other vital activities, increasing up to a critical degree and afterwards declining.(b) The amount of poison reaching the site of action in unit time also varies with the temperature, generally but not always, increasing with its rise. Insect activity, especially locomotor and respiratory, may play an important part in these effects.(c) The apparent effects of temperature on insecticidal action is the combination of these two factors, namely, resistance and pick-up.


2000 ◽  
Vol 125 (4) ◽  
pp. 436-441 ◽  
Author(s):  
Genhua Niu ◽  
Royal D. Heins ◽  
Arthur C. Cameron ◽  
William H. Carlson

Pansy [Viola ×wittrockiana Gams. `Delta Yellow Blotch' (Yellow) and `Delta Primrose Blotch' (Primrose)] plants were grown in a greenhouse under two CO2 concentrations [ambient (≈400 μmol·mol-1) and enriched (≈600 μmol·mol-1)], three daily light integrals (DLI; 4.1, 10.6, and 15.6 mol·m-2·d-1), and nine combinations of day and night temperatures created by moving plants every 12 h among three temperatures (15, 20, and 25 °C). Time to flower decreased and rate of flower development increased as plant average daily temperature (ADT) increased at all DLIs for Yellow or at high and medium DLIs for Primrose. Increasing the DLI from 4.1 to 10.6 mol·m-2·d-1 also decreased time to flower by 4 and 12 days for Yellow and Primrose, respectively. Both cultivars' flower size and Yellow's dry weight [(DW); shoot, flower bud, and total] decreased linearly as plant ADT increased at high and medium DLIs, regardless of how temperature was delivered during day and night. DW in Yellow increased 50% to 100% when DLI increased from 4.1 to 10.6 mol·m-2·d-1 under both CO2 concentrations. Flower size in Yellow and Primrose increased 25% under both CO2 conditions as DLI increased from 4.1 to 10.6 mol·m-2·d-1, but there was no increase between 10.6 and 15.6 mol·m-2·d-1, regardless of CO2 concentration. Plant height and flower peduncle length in Yellow increased linearly as the difference between day and night temperatures (DIF) increased; the increase was larger under lower than higher DLIs. The ratio of leaf length to width (LL/LW) and petiole length in Yellow increased as DIF increased at medium and low DLIs. Carbon dioxide enrichment increased flower size by 4% to 10% and DW by 10% to 30% except for that of the shoot at medium DLI, but did not affect flower developmental rate or morphology. DW of vegetative and reproductive parts of the plant was correlated closely with photothermal ratio, a parameter that describes the combined effect of temperature and light.


2014 ◽  
Vol 32 (1) ◽  
pp. 19-26
Author(s):  
Gary J. Keever ◽  
J. Raymond Kessler ◽  
James C. Stephenson

The effects of bulking duration on growth and flowering of ‘Goldsturm’ black-eyed Susan (Rudbeckia fulgida Ait. ‘Goldsturm’) and ‘Moonbeam’ coreopsis (Coreopsis verticillata L. ‘Moonbeam’) forced into flower under nursery conditions were evaluated as part of a system for the accelerated production of herbaceous perennials requiring long days to flower. Bulking duration treatments were established by a factorialization of potting date (September 24, October 13, December 2, and December 14, 2009) and night-interrupted lighting (NIL) start date (February 1, February 22, and March 15, 2010). Leaf counts of black-eyed Susan at the beginning of NIL increased linearly with progressively longer bulking durations based on potting date and NIL start date, although the effect was more pronounced when compared across potting dates. Based on leaf counts, black-eyed Susan potted in December were still in the juvenile phase when NIL was begun on February 1, 2010. Stem counts of black-eyed Susan at first flower followed a similar pattern as leaf counts. Black-eyed Susan given NIL flowered 40 to 59 days before plants under natural photoperiod (NP). Flower plus flower bud counts of black-eyed Susan at first flower increased linearly with increasing bulking duration based on potting date: by 325, 268, and 243% when NIL was begun on February 1, February 22, and March 15, respectively. Flower counts also increased linearly approximately 46% with increasing bulking duration based on NIL start dates, but only when plants were potted in December. At first flower, plant height of black-eyed Susan given NIL increased linearly as bulking duration increased based on potting date, but did not differ when trended across the NIL start dates. Days to flower of coreopsis decreased with increasing bulking duration, while stem counts increased with bulking duration, and the number of marketable plants was greater when plants were repotted on the three earliest dates compared to those bulked the shortest duration. Effects of bulking duration on flower plus flower bud counts and height of coreopsis were inconsistent.


MRS Advances ◽  
2020 ◽  
Vol 5 (63) ◽  
pp. 3389-3395
Author(s):  
R. González-Díaz ◽  
D. Fernández-Sánchez ◽  
P. Rosendo-Francisco ◽  
G. Sánchez-Legorreta

AbstractIn this work, the first results of the effects of temperature during the production of Se2- ions and the effect during the interaction of Cd2+ and Se2- ions in the synthesis process of CdSe nanoparticles are presented. The synthesis of CdSe was carried out by the colloidal technique, in the first one we used a temperature of 63 °C to produce Se2- ions and in the second one an interaction temperature of 49 °C. The samples were characterized using a Scanning Electron Microscope (SEM) and a Scanning Tunneling Microscope (STM). From the SEM micrographs it was possible to identify the thorns formation and irregular islands. STM micrographs reveal elliptical shapes with a regular electron cloud profile.


Author(s):  
D. T. Gauld ◽  
J. E. G. Raymont

The respiratory rates of three species of planktonic copepods, Acartia clausi, Centropages hamatus and Temora longicornis, were measured at four different temperatures.The relationship between respiratory rate and temperature was found to be similar to that previously found for Calanus, although the slope of the curves differed in the different species.The observations on Centropages at 13 and 170 C. can be divided into two groups and it is suggested that the differences are due to the use of copepods from two different generations.The relationship between the respiratory rates and lengths of Acartia and Centropages agreed very well with that previously found for other species. That for Temora was rather different: the difference is probably due to the distinct difference in the shape of the body of Temora from those of the other species.The application of these measurements to estimates of the food requirements of the copepods is discussed.


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