scholarly journals Modeling the Effect of Temperature on the Flower Development Rate of Hybrid Impatiens

2022 ◽  
Vol 32 (1) ◽  
pp. 16-20
Author(s):  
Mary Vargo ◽  
James E. Faust

The effect of average daily temperature (ADT) on flower bud development and subsequent time to flower was investigated on hybrid impatiens (Impatiens ×hybrida) cultivars Compact Electric Orange, Compact Hot Coral, and Compact Orchid Blush. Plants with a visible flower bud measuring 2 mm in width were placed in one of the four greenhouses with temperature setpoints ranging from 16 to 28 °C. Flower bud width was measured every 3 days in each ADT treatment until flowering. The subsequent days to flower (DTF) from the onset of a visible bud decreased from 36 to 27 days as the ADT increased from 17 to 28 °C. The DTF from visible bud varied by <3 days among the three cultivars across all temperatures; therefore, cultivar data were pooled to create a stronger prediction model. A logistic formula was used to predict the remaining DTF as a function of flower bud width and ADT. The model accurately described the effect of bud width and ADT on flowering time within ±3 days for 87% of the actual DTF across all three cultivars. The resulting flower development model provides greenhouse growers with a guide for manipulating temperature to produce flowering plants for specific market dates based on flower bud width measurements.

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 836B-836
Author(s):  
Carrie DeVier ◽  
Robert L. Geneve

The influence of flowers on root formation in mum cuttings was evaluated for stock plants grown under long (LD) or short (SD) days. SD plants showed visible flower buds after 20 days and color after 30 days. Cuttings were taken from LD or SD plants at 10-day intervals until flowers were fully open. Cuttings from LD plants rooted at 100% throughout the study, with 24 or more roots per cutting. Cuttings from SD plants showed a gradual reduction in rooting percentage and number as flower development increased. After 30 days, roots per cutting for SD plants was reduced by 85% compared to LD cuttings and only 30% of SD cuttings rooted. In a separate experiment, cuttings were taken from stock plants after 40 long or short days. Partial or all flower buds were removed from SD plants prior to sticking. SD cuttings (regardless of flower bud removal) rooted at <47%. LD cuttings rooted between 23.6 to 43.8, while SD cuttings rooted between 3.1 and 8.5 roots per rooted cutting. The data indicates that cuttings taken from flowering plants show reduced potential for rooting and that this effect was not influenced by removal of flowers prior to sticking cuttings.


HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1013A-1013 ◽  
Author(s):  
James E. Faust ◽  
Kelly P. Lewis

Three cultivars of New Guinea impatiens (Impatiens hawkeri) and two cultivars of double impatiens (I. walleriana) were grown in greenhouses maintained at 15, 20, and 25 °C. Bud diameter was measured twice weekly on five plants per cultivar from the time of visible bud to open flower. The experiment was repeated twice. For New Guinea impatiens, the time from visible bud (1-mm diameter) to open flower was 31, 43, and 72 days at 25, 20 and 15 °C, respectively. Flower bud diameter increased linearly as the bud expanded from 1 to 9 mm. For double impatiens, the time from visible bud (1-mm diameter) to open flower was 25, 30, and 58 days at 25, 20 and 15 °C, respectively. Flower bud diameter increased at an increasing rate (curvilinear response) as the bud expanded from 1 to 8 mm. These models are currently in commercial use to aid greenhouse growers in accurately timing crops for specific market dates.


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.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 447f-448
Author(s):  
Millie S. Williams ◽  
Terri Woods Starman ◽  
James E. Faust

Flower growers experience decreased consumer satisfaction with plant species that cease flowering during the summer. The objective of this experiment was to characterize the heat tolerance of four specialty floral crop species in order to predict their summer performance in the different climatalogical regions of the United States. The effect of increasing temperatures on the duration of postharvest flower development was determined for Ageranthemum frutescens `Butterfly' and `Sugar Baby', Brachycome hybrid `Ultra', and Sutera cordata `Snowflake'. Plants were grown in a 18 °C greenhouse until marketable with foliage covering the container and flowers distributed evenly across the plant canopy. Plants were then placed in a phytotron to determine their heat tolerance. Temperature set points of 18, 23, 28, and 33 °C were delivered serially at 2-week intervals, starting at 18 °C. Plants were then returned to 18 °C after the 33 °C treatment. Immature flower bud, mature flower bud, flower and senesced flower numbers were collected once per week. Sutera `Snowflake', and Brachycome `Ultra' had the greatest flower number at the 23 °C temperature, decreasing in the 28 °C environment. Argeranthemum `Butterfly' and `Sugar Baby' had greatest flower number at 28 °C, but flowers were smaller and of lower quality than at 23 °C. Flower development of all cultivars ceased at 33 °C, but when plants were returned to the 18 °C production greenhouse, flower development resumed. According to normal average daily temperatures in Knoxville, Tenn., Ageranthemum frutescens `Butterfly' and `Sugar Baby' would flower until mid-June, while Brachycome hybrid `Ultra' and Sutera cordata `Snowflake' would flower until mid-May.


Insects ◽  
2021 ◽  
Vol 12 (6) ◽  
pp. 508
Author(s):  
Yong-Seok Choi ◽  
Sung-Hoon Baek ◽  
Min-Jung Kim

The predatory gall midge, Feltiella acarisuga (Vallot) (Diptera: Cecidomyiidae), is an acarivorous species that mainly feeds on spider mites (Acarina: Tetranychidae). Because of its cosmopolitan distribution and predation efficacy, it is considered an important natural enemy available as a biological agent for augmentative biocontrol. However, despite its practical use, the thermal development and survival response to temperature have not yet been fully studied. In this study, we investigated the stage-specific development and survival of F. acarisuga at seven temperatures (11.5, 15.7, 19.8, 23.4, 27.7, 31.9, and 35.4 °C) to examine the effect of temperature on its lifecycle. All developmental stages could develop at 11.5–31.9 °C, but the performance was different according to the temperature. From the linear development rate models, the lower development threshold and thermal constant of the total immature stage were estimated at 8.2 °C and 200 DD, respectively. The potential optimal and upper threshold temperatures for the total immature stage were estimated as 29.3 and 35.1 °C using a non-linear development model. The operative thermal ranges for development and survival at 80% of the maximum rate were 24.5–32.3 and 14.7–28.7 °C, respectively. Thus, it was suggested that 24.5–28.7 °C was suitable for the total immature stage. In contrast, conditions around 8 °C and 35 °C should be avoided due to the lower development rate and high mortality. Our findings provide fundamental information for an effective mass-rearing and releasing program of F. acarisuga in an augmentative biocontrol program and help to predict phenology.


1991 ◽  
Vol 39 (2) ◽  
pp. 191 ◽  
Author(s):  
JG Hamilton ◽  
MP Zalucki

C. plebejana were reared from egg to adult at a range of constant temperatures. At 10-degrees-C no immature stages survived. Development rates increased over the temperature range 14-34-degrees-C; these were simulated with a non-linear model. Females emerged before males. Fecundity decreased with increased rearing temperature as a direct result of reduced adult female weight. At 34-degrees-C development rate and survival were reduced and all eggs laid were infertile. Optimum temperature for population increase was 28-degrees-C. Validation of a non-linear model for development rate shows that the species of host-plant affects mean development rates of tipworm. Although 5.3 tipworm generations are possible on cotton annually, only one occurs; reasons for this are suggested.


2018 ◽  
Vol 70 (3) ◽  
pp. 937-948 ◽  
Author(s):  
Faline D M Plantenga ◽  
Sara Bergonzi ◽  
José A Abelenda ◽  
Christian W B Bachem ◽  
Richard G F Visser ◽  
...  

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