Epigenetic repression and resetting of a floral repressor, FLC, in the life cycle of winter-annual Arabidopsis

2021 ◽  
Author(s):  
Dong-Hwan Kim
Keyword(s):  
Life Cycle ◽  
Floral Repressor ◽  
Winter Annual ◽  
Epigenetic Repression

Delayed germination in seeds of Phacelia dubia var. dubia

1973 ◽  
Vol 51 (12) ◽  
pp. 2481-2486 ◽  
Author(s):  
Jerry M. Baskin ◽  
Carol C. Baskin
Keyword(s):  
Life Cycle ◽  
Seedling Establishment ◽  
Winter Temperature ◽  
Seed Crop ◽  
Temperature Conditions ◽  
Secondary Dormancy ◽  
Winter Temperatures ◽  
Winter Annual ◽  
Delayed Germination ◽  
Germinating Seeds

Not all seeds of a particular seed crop of the winter annual Phacelia dubia var. dubia germinate the first autumn after their dispersal in spring, and germination of a given seed crop is spread over several years. Nondormant seeds that do not germinate in autumn are induced into secondary dormancy by low winter temperatures and must afterripen again during summer before they are capable of germinating. Seeds that do not afterripen the first summer after dispersal are prevented from doing so until at least the next summer because winter temperature conditions prevent afterripening. These responses of the seeds to the environment insure that germination will occur only in autumn, the only season of the year that is suitable for seedling establishment and eventual completion of the life cycle.

Long-term effects of 2,4-D application on plants. II. Herbicide avoidance by Chenopodium album and Thlaspi arvense

1988 ◽  
Vol 66 (2) ◽  
pp. 230-235 ◽  
Author(s):  
Larry Hume
Keyword(s):  
Life Cycle ◽  
Chenopodium Album ◽  
Herbicide Tolerance ◽  
Long Term Effects ◽  
Annual Life Cycle ◽  
Thlaspi Arvense ◽  
Immature Seeds ◽  
Winter Annual ◽  
Dichlorophenoxy Acetic Acid

Research plots in a wheat–wheat–fallow rotation at Indian Head, Sask., were sprayed annually with 2,4-dichlorophenoxy-acetic acid (2,4-D) for 36 consecutive years. Two species susceptible to 2,4-D, Chenopodium album L. and Thlaspi arvense L., were dominant in these plots. From 1981 to 1983, C. album and T. arvense seedlings that emerged during four periods of the growing season were marked and their mortality, seed production, and size recorded. From these data and other studies, 10 ways in which C. album and T. arvense managed to survive herbicide application were identified. These are intermittent germination, herbicide tolerance, small size of late-emerging seedlings, short life cycle, hardiness, failure of control practices, long-term dormancy, seed dispersal, viability of immature seeds, and winter annual life cycle of T. arvense.

Intermediate morphophysiological dormancy allows for life-cycle diversity in the annual weed, Turgenia latifolia (Apiaceae)

2014 ◽  
Vol 62 (8) ◽  
pp. 630 ◽  
Author(s):  
Miregul Nurulla ◽  
Carol C. Baskin ◽  
Juan J. Lu ◽  
Dun Y. Tan ◽  
Jerry M. Baskin
Keyword(s):  
Life Cycle ◽  
Low Temperatures ◽  
Western China ◽  
Intermediate Complex ◽  
Dormancy Breaking ◽  
Morphophysiological Dormancy ◽  
Temperature Regimes ◽  
Germination Phenology ◽  
Physiological Dormancy ◽  
Winter Annual

Our aim was to determine the seed dormancy-breaking requirements and type of life cycle of Turgenia latifolia in north-western China. At dispersal in July, only 0–9% of the seeds germinated at 5/2°C, 15/2°C, 20/10°C and 25/15°C; thus, 91% of the seeds exhibited physiological dormancy (PD) and 9% were non-dormant. Also, the embryo was underdeveloped and embryo length : seed length ratio increased from 0.38 in fresh seeds to 0.79 at germination. Seeds buried in dry soil at the four temperature regimes for 12 weeks germinated to ≥50% when tested in darkness at 5/2°C, and those buried at 15/2°C and 20/10°C germinated to ≥50% when tested at 15/2°C. Seeds have intermediate complex morphophysiological dormancy (MPD). PD was broken at high and/or low temperatures, but embryo growth was completed only at low temperatures; gibberellic acid (GA3) promoted germination. Seeds buried under natural conditions during summer germinated to ~70% and ~55% at 5/2°C and 15/2°C, respectively, in darkness in autumn. In a germination-phenology study, cumulative germination was ~20% and ~80% in autumn and spring, respectively. Intermediate complex MPD allows the species to behave as a winter annual and as a short-lived summer annual.

Growth Response to Different Levels of Soil Moisture and Soil Fertility in Four Winter Annual Species during Their Life-Cycle

Flora ◽  
1990 ◽  
Vol 184 (4) ◽  
pp. 303-312 ◽  
Author(s):  
N.A.M.G. Rozijn ◽  
W.H.O. Ernst ◽  
J. van Andel ◽  
H.J.M. Nelissen
Keyword(s):  
Soil Moisture ◽  
Life Cycle ◽  
Soil Fertility ◽  
Growth Response ◽  
Annual Species ◽  
Winter Annual ◽  
Different Levels

Ecological life cycle and physiological ecology of seed germination of Arabidopsis thaliana

1972 ◽  
Vol 50 (2) ◽  
pp. 353-360 ◽  
Author(s):  
Jerry M. Baskin ◽  
Carol C. Baskin
Keyword(s):  
Arabidopsis Thaliana ◽  
Life Cycle ◽  
Physiological Responses ◽  
Natural Habitat ◽  
Maximum Temperature ◽  
Constant Darkness ◽  
Optimum Temperature ◽  
Summer Period ◽  
Arid Habitat ◽  
Winter Annual

Field observations were made on the ecological life cycle of the winter annual Arabidopsis thaliana (L.) Heyn. from a population in central Tennessee, and a detailed laboratory study was conducted on the physiological responses of the seeds to temperature in light (14-h photoperiod) and constant darkness. At maturity and dispersal (late April and early May), seeds germinated to high percentages only at low temperatures (5–10 °C) in light. With storage from May to September and October (1) the maximum temperature for germination in light increased from 15 to 30 °C and in darkness from 10 to 20 °C and (2) the optimum temperature for germination in light increased from 5 to 15–20 °C and in darkness from 5 to 5–10 °C. During the spring–summer period seeds were dormant at temperatures simulating those in the natural habitat. In September and October, seeds in light germinated to high percentages at simulated September and October temperatures but did not germinate in darkness at the September temperatures and germinated poorly at October temperatures. Regulation of germination so that it occurs in early autumn allows A. thaliana to persist in a summer-arid habitat.

scholarly journals Changes in phenological events in response to a global warming scenario reveal greater adaptability of winter annual compared with summer annual arabidopsis ecotypes

2020 ◽  
Vol 127 (1) ◽  
pp. 111-122
Author(s):  
Steven Footitt ◽  
Angela J Hambidge ◽  
William E Finch-Savage
Keyword(s):  
Global Warming ◽  
Life Cycle ◽  
Seedling Emergence ◽  
Plant Size ◽  
Annual Plant ◽  
Warming Scenario ◽  
Summer Temperatures ◽  
Global Warming Scenario ◽  
Winter Annual ◽  
The Impact

Abstract Background and Aims The impact of global warming on life cycle timing is uncertain. We investigated changes in life cycle timing in a global warming scenario. We compared Arabidopsis thaliana ecotypes adapted to the warm/dry Cape Verdi Islands (Cvi), Macaronesia, and the cool/wet climate of the Burren (Bur), Ireland, Northern Europe. These are obligate winter and summer annuals, respectively. Methods Using a global warming scenario predicting a 4 °C temperature rise from 2011 to approx. 2080, we produced F1 seeds at each end of a thermogradient tunnel. Each F1 cohort (cool and warm) then produced F2 seeds at both ends of the thermal gradient in winter and summer annual life cycles. F2 seeds from the winter life cycle were buried at three positions along the gradient to determine the impact of temperature on seedling emergence in a simulated winter life cycle. Key Results In a winter life cycle, increasing temperatures advanced flowering time by 10.1 d °C–1 in the winter annual and 4.9 d °C–1 in the summer annual. Plant size and seed yield responded positively to global warming in both ecotypes. In a winter life cycle, the impact of increasing temperature on seedling emergence timing was positive in the winter annual, but negative in the summer annual. Global warming reduced summer annual plant size and seed yield in a summer life cycle. Conclusions Seedling emergence timing observed in the north European summer annual ecotype may exacerbate the negative impact of predicted increased spring and summer temperatures on their establishment and reproductive performance. In contrast, seedling establishment of the Macaronesian winter annual may benefit from higher soil temperatures that will delay emergence until autumn, but which also facilitates earlier spring flowering and consequent avoidance of high summer temperatures. Such plasticity gives winter annual arabidopsis ecotypes a distinct advantage over summer annuals in expected global warming scenarios. This highlights the importance of variation in the timing of seedling establishment in understanding plant species responses to anthropogenic climate change.

Ultrastructural analysis of “Sensory” surface nerve endings and “putative” neurotransmitter sites in Schistosoma mansoni Miracidia

1989 ◽  
Vol 47 ◽  
pp. 962-963
Author(s):  
Betty Ruth Jones ◽  
Steve Chi-Tang Pan
Keyword(s):  
Nervous System ◽  
Life Cycle ◽  
Schistosoma Mansoni ◽  
Snail Host ◽  
Complex Life Cycle ◽  
Rational Approach ◽  
Effective Control ◽  
The Social ◽  
Social And Economic Development ◽  
Basic Biology

INTRODUCTION: Schistosomiasis has been described as “one of the most devastating diseases of mankind, second only to malaria in its deleterious effects on the social and economic development of populations in many warm areas of the world.” The disease is worldwide and is probably spreading faster and becoming more intense than the overall research efforts designed to provide the basis for countering it. Moreover, there are indications that the development of water resources and the demands for increasing cultivation and food in developing countries may prevent adequate control of the disease and thus the number of infections are increasing.Our knowledge of the basic biology of the parasites causing the disease is far from adequate. Such knowledge is essential if we are to develop a rational approach to the effective control of human schistosomiasis. The miracidium is the first infective stage in the complex life cycle of schistosomes. The future of the entire life cycle depends on the capacity and ability of this organism to locate and enter a suitable snail host for further development, Little is known about the nervous system of the miracidium of Schistosoma mansoni and of other trematodes. Studies indicate that miracidia contain a well developed and complex nervous system that may aid the larvae in locating and entering a susceptible snail host (Wilson, 1970; Brooker, 1972; Chernin, 1974; Pan, 1980; Mehlhorn, 1988; and Jones, 1987-1988).

A freeze-fracture-etched study of the physarum polycephalum plasma membrane during early formation of the macroplasmodial stage

1993 ◽  
Vol 51 ◽  
pp. 346-347
Author(s):  
Randolph W. Taylor ◽  
Henrie Treadwell
Keyword(s):  
Plasma Membrane ◽  
Life Cycle ◽  
Growth Phase ◽  
Filter Paper ◽  
Physarum Polycephalum ◽  
Freeze Fracture ◽  
Petri Dish ◽  
Wire Screen ◽  
Wide Mouth ◽  
Sterile Filter

The plasma membrane of the Slime Mold, Physarum polycephalum, process unique morphological distinctions at different stages of the life cycle. Investigations of the plasma membrane of P. polycephalum, particularly, the arrangements of the intramembranous particles has provided useful information concerning possible changes occurring in higher organisms. In this report Freeze-fracture-etched techniques were used to investigate 3 hours post-fusion of the macroplasmodia stage of the P. polycephalum plasma membrane.Microplasmodia of Physarum polycephalum (M3C), axenically maintained, were collected in mid-expotential growth phase by centrifugation. Aliquots of microplasmodia were spread in 3 cm circles with a wide mouth pipette onto sterile filter paper which was supported on a wire screen contained in a petri dish. The cells were starved for 2 hrs at 24°C. After starvation, the cells were feed semidefined medium supplemented with hemin and incubated at 24°C. Three hours after incubation, samples were collected randomly from the petri plates, placed in plancettes and frozen with a propane-nitrogen jet freezer.

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