scholarly journals Effect of Low-intensity Red and Far-red Light and High-intensity White Light on the Flowering Response of the Long-day Plant Lemna gibba G3

1968 ◽  
Vol 43 (2) ◽  
pp. 157-162 ◽  
Author(s):  
Charles F. Cleland ◽  
Winslow R. Briggs
Keyword(s):  
White Light ◽  
High Intensity ◽  
Red Light ◽  
Lemna Gibba ◽  
Flowering Response ◽  
Low Intensity ◽  
Long Day

Variability in photoperiod and the inhibition of flowering in a high latitude population of Saxifraga rivularis

1981 ◽  
Vol 59 (3) ◽  
pp. 388-391 ◽  
Author(s):  
J. A. Teeri ◽  
S. J. Tonsor
Keyword(s):  
High Latitude ◽  
High Intensity ◽  
Dark Period ◽  
Controlled Environment ◽  
Photoperiodic Control ◽  
Incandescent Light ◽  
Devon Island ◽  
Low Intensity ◽  
Long Day ◽  
Long Day Plants

A population of Saxifraga rivularis L. collected at Truelove Lowland, Devon Island, N.W.T., Canada (75°41′ N) exhibits a photoperiodic control of flowering in controlled environment chambers. The plants respond in a manner typical of long-day plants with flowering inhibited by either a 6-h daily dark period, or by a 6-h daily low intensity irradiance regime of incandescent light. The inhibition of flowering by 6 h day−1 of incandescent light does not occur if the incandescent light is given in twelve 0.5-h doses, each followed by 1 h of red-rich high intensity irradiance.

scholarly journals 631 Photocontrol of Flowering and Stem Extension of the Intermediate-day Plant Echinacea purpurea Moench.

HortScience ◽  
2000 ◽  
Vol 35 (3) ◽  
pp. 506C-506
Author(s):  
Erik S. Runkle ◽  
Royal D. Heins ◽  
Arthur C. Cameron ◽  
William H. Carlson
Keyword(s):  
Red Light ◽  
Echinacea Purpurea ◽  
Physiological Age ◽  
Stem Length ◽  
Low Intensity ◽  
Stem Extension ◽  
Long Day ◽  
Short Days

Intermediate-day plants (IDP) flower most rapidly and completely under intermediate photoperiods (e.g., 12 to 14 h of light), but few species have been identified and their flowering responses are not well understood. A variety of experiments was conducted to determine how light controls flowering and stem extension of Echinacea purpurea `Bravado' and `Magnus'. Both cultivars flowered most completely (79%) and rapidly and at the youngest physiological age under intermediate photoperiods of 13 to 15 h. Few (14%) plants flowered under 10- or 24-h photoperiods, indicating E. purpurea is a qualitative IDP. Plants were also induced to flower when 15-h dark periods were interrupted with as few as 7.5 min of low-intensity lighting (night interruption, NI). Flowering was progressively earlier as the NI increased to 1 h, but was delayed when the NI was extended to 4 h. Stem length increased by 230% as the photoperiod or NI duration increased, until plants received a saturating duration (at 14 h or 1 h, respectively). At macroscopic visible bud, transferring plants from long days to short days reduced stem extension by up to 30%. Flowering was inhibited when the entire photoperiod was deficient in blue or red light and was promoted in a far-red deficient environment, suggesting that phytochrome and cryptochrome control flowering of E. purpurea. Because of our results, we propose the flowering behavior of IDP such as E. purpurea is composed of two mechanisms: a dark-dependent response in which flowering is promoted by a short night, and a light-dependent response in which flowering is inhibited by a long day.

scholarly journals Investigation of transient eye closure evoked with bright light in the patients with intermittent exotropia

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Won Jong Choi ◽  
Yeonji Jang ◽  
Seong-Joon Kim ◽  
Jae Ho Jung
Keyword(s):  
White Light ◽  
High Intensity ◽  
Near Infrared ◽  
Bright Light ◽  
Infrared Camera ◽  
Monitor System ◽  
Intermittent Exotropia ◽  
Simple Method ◽  
Low Intensity ◽  
Eye Closure

Abstract Background This study aimed to present a simple method for evaluating transient eye closure (TEC) evoked by bright light and find the agreement between TEC and photosensitivity. We also assessed the associated factors with TEC in the patients with intermittent exotropia (IXT). Methods In this retrospective study, IXT patients were exposed to different brightness: darkness, low-intensity white light, and high-intensity white light using a near-infrared camera vision monitor system (Mon CV3, Metrovision, France). TEC was considered to be present if the subject closed his or her eyes immediately, and for more than half of the scotopic lid fissure distance in response to the high-intensity or low-intensity photopic stimulus of light, compared with lid fissure distance in the scotopic phase. We assessed the presence of photosensitivity using a questionnaire and evaluated the agreement between TEC and photosensitivity. We also investigated the sensory fusion, motor fusion, and pupil dynamic components for the existence of TEC in IXT patients. Results Sixty-one patients with IXT were included. With the new method to evaluate TEC under different light intensities, 27 (44.3%) of the 61 IXT patients showed TEC, and 34 (55.7%) did not demonstrate TEC. TEC under high-intensity white light had a strong correlation with self-reporting photosensitivity (r = 0.77). The smaller angle of deviation at near was associated with the presence of TEC, with statistical significance (p = 0.04). Normal sensory status at a distance was significantly associated with TEC (p <  0.01). Multivariate analysis using multiple logistic regression analysis showed that normal sensory status was significantly associated with TEC (p = 0.02). Conclusions The test using a near-infrared camera vision monitor system was a simple and objective tool in identifying TEC evoked by bright light. The presence of TEC strongly correlated with self-reporting photosensitivity in patients with IXT. However, TEC may be an independent phenomenon with motor alignment, stereopsis, and pupil reflex pathway in patients with IXT.

scholarly journals Carotenoid Production by Dunaliella salina under Red Light

Antioxidants ◽  
2019 ◽  
Vol 8 (5) ◽  
pp. 123 ◽  
Author(s):  
Yanan Xu ◽  
Patricia J. Harvey
Keyword(s):  
Blue Light ◽  
White Light ◽  
High Intensity ◽  
Dunaliella Salina ◽  
Red Light ◽  
Carotenoid Biosynthesis ◽  
High Rate ◽  
Carotenoid Content ◽  
Photon Flux ◽  
Carotenoid Accumulation

The halotolerant photoautotrophic marine microalga Dunaliella salina is one of the richest sources of natural carotenoids. Here we investigated the effects of high intensity blue, red and white light from light emitting diodes (LED) on the production of carotenoids by strains of D. salina under nutrient sufficiency and strict temperature control favouring growth. Growth in high intensity red light was associated with carotenoid accumulation and a high rate of oxygen uptake. On transfer to blue light, a massive drop in carotenoid content was recorded along with very high rates of photo-oxidation. In high intensity blue light, growth was maintained at the same rate as in red or white light, but without carotenoid accumulation; transfer to red light stimulated a small increase in carotenoid content. The data support chlorophyll absorption of red light photons to reduce plastoquinone in photosystem II, coupled to phytoene desaturation by plastoquinol:oxygen oxidoreductase, with oxygen as electron acceptor. Partitioning of electrons between photosynthesis and carotenoid biosynthesis would depend on both red photon flux intensity and phytoene synthase upregulation by the red light photoreceptor, phytochrome. Red light control of carotenoid biosynthesis and accumulation reduces the rate of formation of reactive oxygen species (ROS) as well as increases the pool size of anti-oxidant.

Photoperiodism and rhythmic flower induction: complete substitution of inductive darkness by light

1969 ◽  
Vol 47 (8) ◽  
pp. 1241-1250 ◽  
Author(s):  
Bruce G. Cumming
Keyword(s):  
White Light ◽  
High Intensity ◽  
Dark Period ◽  
Flower Induction ◽  
Flower Initiation ◽  
Response Type ◽  
Short Day ◽  
Long Day ◽  
Sufficient Energy ◽  
Promotive Effect

In a short-day response type of Chenopodium rubrum (ecotype 60°47′ N), light of a relatively low red/far-red ratio—but of sufficient energy to allow photosynthesis—can bring about induction of flowering when it completely replaces a single dark period interrupting continuous white light. When high-intensity white incandescent light was interrupted for less than a 24-hour period, a longer period of inductive light than darkness was required even for minimal induction. An inductive light interruption of at least 60 hours was required for 100% flower induction. The result of such forcing of the system by inductive light, as compared with the circadian rhythmic induction that occurred in darkness, was a change towards a more linear inductive response and there were indications (requiring confirmation) of oscillations of higher frequency.When seedlings were maintained continuously in optimal inductive light or in darkness, after an initial high intensity white light period, there was some flower initiation within 5 days in inductive light, but not until about 10 days in darkness, and then only when sucrose was supplied throughout darkness.There were suboptimal and (inhibitory) supraoptimal effects on induction when the R/FR ratio and (or) the energy of inductive light were decreased or increased, respectively. These results, in conjunction with the effects that were obtained when glucose and 3(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) were applied in inductive light as compared with darkness, implicate both photosynthate and phytochrome-Pfr as having a positive (promotive) effect during normal inductive darkness.These findings emphasize that the important controls in photoperiodism and flowering may be quantitative rather than qualitative in character, because it can now be questioned whether there is any essential dark-requiring reaction in the induction not only of long-day but also of short-day plants.

Inhibition rather than Enhancement of Hemostatic System Activation during Initiation of Oral Anticoagulant Treatment

1997 ◽  
Vol 77 (04) ◽  
pp. 685-689 ◽  
Author(s):  
Paul A Kyrle ◽  
Johannes Brockmeier ◽  
Ansgar Weltermann ◽  
Sabine Eichinger ◽  
Wolfgang Speiser ◽  
...  
Keyword(s):  
High Intensity ◽  
Oral Anticoagulant ◽  
Protein C ◽  
Venous Blood ◽  
Rapid Decline ◽  
Oral Anticoagulant Treatment ◽  
Shed Blood ◽  
Low Intensity ◽  
Hemostatic System ◽  
System Activation

SummaryCoumarin-induced skin necrosis is believed to be due to a transient hypercoagulable state resulting from a more rapid decline of the protein C activity relative to that of coagulation factors (F) II, IX and X during initiation of oral anticoagulant therapy. We studied hemostatic system activation during early oral anticoagulant treatment with a technique that investigates coagulation activation in the microcirculation.We determined in 10 healthy volunteers the concentrations of prothrombin fragment F1+2 (f1.2) and thrombin-antithrombin complex (TAT) in blood emerging from an injury of the microvasculature (bleeding time incision) before and after initiation of both high-inten- sity and low-intensity coumarin therapy. In addition, f1.2, TAT, activated F VII (F Vila) and the activities of FII, F VII, F X and protein C were measured in venous blood.A rapid decline of F VII and protein C was observed in venous blood with activities at 24 h of 7 ± 1% and 43 ± 2%, respectively, during the high-intensity regimen. A 20 to 30% reduction of f1.2 and TAT was seen in venous blood at 72 h with no major difference between the high- and the low-intensity regimen. F Vila levels were substantially affected by anticoagulation with a >90% reduction at 48 h during the high-intensity regimen. Following high-intensity coumarin, a >50% decrease in the fl.2 and TAT levels was found in shed blood at 48 h suggesting substantial inhibition of thrombin generation during early oral anticoagulation. An increase in the f1.2 and TAT levels was seen neither in shed blood nor in venous blood.Our data do not support the concept of a transient imbalance between generation and inhibition of thrombin as the underlying pathomechanism of coumarin-induced skin nekrosis.

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