Flowering in Townsville lucerne (Stylosanthes humilis). 1. Studies in controlled environments

1967 ◽  
Vol 7 (29) ◽  
pp. 489 ◽  
Author(s):  
DF Cameron

The flowering of seven selections of Townsville lucerne (Stylosanthes humilis HBK) representing a range of maturity types has been studied in the Canberra phytotron. Daylength is the main factor controlling flowering in these selections, all of which showed a strong short day response. At normal temperatures the maximum daylengths at which all plants flowered (the critical daylengths) were 13 hours for the early, 12 hours for the midseason and late-midseason, and 11 1/2 hours for the late selections. However, the midseason selections did flower in a 12 1/2-hour daylength if the light intensity of the supplementary illumination was 20 or 5 ft.c. instead of the normal 50 ft.c. The response of the other selections was not altered at the lower light intensities. Both high night temperature and low day temperature delayed or inhibited flower initiation in the early and midseason selections and these effects were greater at a critical daylength.

HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 648d-648
Author(s):  
Jack W. Buxton ◽  
Donna Switzer ◽  
Guoqiang Hou

Marigold seedlings, 3 weeks old, were grown in natural light growth chambers at 3 day/night temperature regimes, 8°N/16°D, 13°N/20°D and 18°N/24°D, in a factorial combination with ambient and 1000-1500 ppm CO2. Seedlings were harvested at regular intervals during a 24 hr period and were analyzed for soluble sugars (reducing sugars and sucrose) and starch. Neither temperature nor CO2 concentration affected the accumulation of soluble sugars or starch during the day or night. The soluble sugar concentration ranged from 3% of dry weight at sunrise to 6% at mid-day; the concentration changed little during the night. Light intensity was different during replications of the experiment. Increased light intensity appeared to cause a slight increase in the soluble sugars maintained by the seedling during the day. Accumulated starch increased 6% to 8% from sunrise to late afternoon. Preliminary results indicate that light intensity greatly affected the concentration of starch. On the higher light intensity day, starch accumulated to a maximum of 18% of dry weight; whereas on the lower light intensity day the maximum concentration was 10%. During the night following the lower light intensity day, the starch concentration decreased to approximately 3% by the end of the night; following a brighter day the starch content was 13% at the end of the night.


2017 ◽  
Vol 86 (2) ◽  
Author(s):  
Waldemar Kiszczak ◽  
Urszula Kowalska ◽  
Agata Kapuścińska ◽  
Maria Burian ◽  
Krystyna Górecka

Doubled haploid lines of carrot can be obtained through androgenesis in anther cultures and in isolated microspore cultures. The two methods were compared using three carrot cultivars (‘Kazan F1’, ‘Feria F1’, and ‘Narbonne F1’) at the androgenesis induction stage, during plant regeneration from embryos, and during acclimatization of androgenetic plants as well as their characterization. It was found that cultivar was the main factor affecting the efficiency at each stage of plant production in both anther and isolated microspore cultures. The efficiency of androgenesis in anther cultures of ‘Feria F1’ was considerably higher in comparison with isolated microspore cultures, and more plants were obtained from the embryos of androgenesis-cultured plants. In ‘Kazan F1’ and ‘Narbonne F1’, more acclimatized androgenetic plants were produced from anther cultures. Ploidy assessment of acclimatized plants of ‘Narbonne F1’ showed that the majority of the plants in the population derived from anther cultures had a doubled chromosome (DH) set. On the other hand, the majority of plants obtained from isolated microspore cultures were haploids. When assessing homozygosity, it was found among plants obtained in anther cultures that the percentage of homozygotes for phosphoglucose isomerase (PGI) and aspartate aminotransferase (AAT) depended on the cultivar. In contrast, the majority of plants derived from isolated microspore cultures were homozygous regardless of cultivar.


2003 ◽  
Vol 128 (4) ◽  
pp. 479-485 ◽  
Author(s):  
Erik S. Runkle ◽  
Royal D. Heins

Plastics that selectively reduce the transmission of far-red light (FR, 700 to 800 nm) reduce extension growth of many floricultural crops. However, FR-deficient (FRd) environments delay flowering in some long-day plants (LDPs), including `Crystal Bowl Yellow' pansy (Viola ×wittrockiana Gams). Our objective was to determine if FR light could be added to an otherwise FRd environment to facilitate flowering with minimal extension growth. In one experiment, plants were grown under a 16-hour FRd photoperiod, and FR-rich light was added during portions of the day or night. For comparison, plants were also grown with a 9-hour photoperiod [short-day (SD) control] or under a neutral (N) filter with a 16-hour photoperiod (long day control). Flowering was promoted most (i.e., percent of plants that flowered increased and time to flower decreased) when FR-rich light was added during the entire 16-hour photoperiod, during the last 4 hours of the photoperiod, or during the first or second 4 hours after the end of the photoperiod. In a separate experiment, pansy was grown under an FRd or N filter with a 9-hour photoperiod plus 0, 0.5, 1, 2, or 4 hours of night interruption (NI) lighting that delivered a red (R, 600 to 700 nm) to FR ratio of 0.56 (low), 1.28 (moderate), or 7.29 (high). Under the N filter, the minimum NI duration that increased percent flowering was 2 hours with a moderate or low R:FR and 4 hours with a high R:FR. Under the FRd filter, 2 or 4 hours of NI lighting with a moderate or low R:FR, respectively, was required to increase percent flowering, but a 4-hour NI with a high R:FR failed to promote flowering. Pansy appears to be day-neutral with respect to flower initiation and a quantitative LDP with respect to flower development. The promotion of reproductive development was related linearly to the promotion of extension growth. Therefore, it appears that in LDPs such as pansy, light duration and quality concomitantly promote extension growth and flowering, and cannot readily be separated with lighting strategies.


2021 ◽  
Vol 11 ◽  
Author(s):  
Malleshaiah SharathKumar ◽  
Ep Heuvelink ◽  
Leo F. M. Marcelis ◽  
Wim van Ieperen

Shorter photoperiod and lower daily light integral (DLI) limit the winter greenhouse production. Extending the photoperiod by supplemental light increases biomass production but inhibits flowering in short-day plants such as Chrysanthemum morifolium. Previously, we reported that flowering in growth-chamber grown chrysanthemum with red (R) and blue (B) LED-light could also be induced in long photoperiods by applying only blue light during the last 4h of 15h long-days. This study investigates the possibility to induce flowering by extending short-days in greenhouses with 4h of blue light. Furthermore, flower induction after 4h of red light extension was tested after short-days RB-LED light in a growth-chamber and after natural solar light in a greenhouse. Plants were grown at 11h of sole source RB light (60:40) in a growth-chamber or solar light in the greenhouse (short-days). Additionally, plants were grown under long-days, which either consisted of short-days as described above extended with 4h of B or R light to long-days or of 15h continuous RB light or natural solar light. Flower initiation and normal capitulum development occurred in the blue-extended long-days in the growth-chamber after 11h of sole source RB, similarly as in short-days. However, when the blue extension was applied after 11h of full-spectrum solar light in a greenhouse, no flower initiation occurred. With red-extended long-days after 11h RB (growth-chamber) flower initiation occurred, but capitulum development was hindered. No flower initiation occurred in red-extended long-days in the greenhouse. These results indicate that multiple components of the daylight spectrum influence different phases in photoperiodic flowering in chrysanthemum in a time-dependent manner. This research shows that smart use of LED-light can open avenues for a more efficient year-round cultivation of chrysanthemum by circumventing the short-day requirement for flowering when applied in emerging vertical farm or plant factories that operate without natural solar light. In current year-round greenhouses’ production, however, extension of the natural solar light during the first 11 h of the photoperiod with either red or blue sole LED light, did inhibit flowering.


1972 ◽  
Vol 50 (6) ◽  
pp. 713-719 ◽  
Author(s):  
William E. Bradshaw ◽  
L. Philip Lounibos

Wyeomyia smithii diapause in the third larval instar. Long days avert or terminate and short days promote or maintain diapause. Diapause occurs early in the third instar and may be terminated by photoperiodic stimuli without the intervention of chilling or other factors. Fifty percent termination of diapause requires about 3 long days and another [Formula: see text] days are consumed in the third instar for postdiapause development. The critical daylength is identical for both the initiation and termination of diapause, 14.75 h of light per day. But, the photoperiodic clock monitoring diapause decisions is several times as accurate during initiation as in termination, reflecting the more drastic environmental consequences of development misdirection in the fall than in the spring. This accuracy is further enhanced by a prolongation of the second instar under short-day conditions. The doubling in the duration of the second instar exhibits the same critical daylength properties as diapause determination.The third instar is divisible into four distinct developmental periods: prediapause, diapause, termination of diapause, and postdiapause. Methods for quantifying these periods are presented. Similar manipulations could be employed for other diapausing arthropods, regardless of the stage at which dormancy occurs or the cues used in its regulation.


1965 ◽  
Vol 16 (1) ◽  
pp. 1 ◽  
Author(s):  
RD Asana ◽  
RF Williams

Experiments were conducted in controlled environments to determine the effects of high temperatures on grain development and yield in wheat. Two Australian and three Indian cultivars of wheat were exposed, from a week after anthesis until maturity, to "day" temperatures of 25, 28, and 3l°C, and "night" temperatures of 9 and 12°C. There was a mean reduction in yield of 16%' for the 6° rise in day temperature, but the cultivars did not differ significantly in their response to these temperatures. There were no significant effects of night temperature on grain weight, but stem weight was less at 12°C. Senescence was hastened only slightly by high day temperature, and there were no differential effects between cultivars in this respect.In a subsidiary experiment one Indian and five Australian cultivars were subjected to three day-night temperature regimes (24/19°, 27/22°, and 30/25°C). Highly significant but complex interactions were established between temperature regime and cultivar. A growth analysis for the Australian cultivars Ridley and Diadem indicated that the developing grain of Ridley had a greater capacity for growth than that of Diadem from the earliest stage. This, together with the confirmation of grain size as a very stable characteristic for all the varieties, points to the developmental and synthetic activity of the grain as an important determinant of grain yield. The relevance of this study to the production of wheat in India is briefly discussed.


1971 ◽  
Vol 49 (6) ◽  
pp. 855-862 ◽  
Author(s):  
Nelson H. F. Watson ◽  
B. N. Smallman

Daylength and temperature were shown to be environmental cues which interact to cause an arrest in development at the fourth copepodite instar of two cohabiting, temporary pond species of the genus Diacyclops; D. navus Herrick, and a second species of uncertain specific designation. The first species entered arrest under short-day conditions, the latter under long days. Arrest did not occur in rearings conducted in either continuous light or complete darkness. Cyclopids were sensitive to the photoperiodic stimulus only during the first copepodite instar. Temperature was shown to affect the critical daylength values associated with a transition from a long-day to a short-day response for each species.Similarities with insect diapause and the ecological implications of the response are discussed.


2020 ◽  
Vol 65 (No. 2) ◽  
pp. 41-50
Author(s):  
Lucia Mačuhová ◽  
Vladimír Tančin ◽  
Juliana Mačuhová

Milking frequency is the main factor regulating milk yield and milk quality if feeding, welfare, health, and environmental conditions are adequate. Milk yield and composition are substantially influenced by breed, and consequently the breed has an impact on both factors at a different frequency of milking. Further, the size of cisternal compartment plays an important role in accommodating secreted milk between milkings. Thus, ewes with large cisterns (i.e. large cisternal area, high cisternal milk percentage, and delayed tight junction opening during milk stasis) adapt themselves better to longer milking intervals than ewes with a small cistern. The increase of milking frequency from two to three times a day can lead to an increase of milk yield in the range of 3 to 36%. On the other hand, the reduction of milking frequency from twice to once a day can decrease milk yield from 9 to 67%. Two milkings per week could be omitted with no negative effects on milk yield, milk composition, and somatic cell count in ewes with large cisterns. However, besides the breed and cistern storage capacity, the results in literature show that the effects of milking frequency on milk yield and milk composition can vary according to the stage of lactation, individual animal, production level, practice of stripping, and duration of changed frequency. The right use of different milking frequency strategies can result in increased milk yield or in significant savings in labour and time spent in the milking parlour with negligible or no negative effects on milk yield and composition.


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