Regreening of involucral leaves of female Leucadendron (Proteaceae) after flowering

2010 ◽  
Vol 58 (7) ◽  
pp. 586 ◽  
Author(s):  
M. Schmeisser ◽  
W. J. Steyn ◽  
G. Jacobs
Keyword(s):  
Light Intensity ◽  
Photosynthetic Pigments ◽  
Colour Change ◽  
Complete Removal ◽  
High Light Intensity ◽  
High Light ◽  
Growth Chamber ◽  
Full Bloom ◽  
Yellow Colour ◽  
Plastid Envelope

Involucral leaves of Leucadendron have the remarkable ability to turn yellow upon flowering and regreen naturally as the florets of the inflorescence wilt. This colour change results from degradation of chlorophyll and to a lesser degree carotenoids, resulting in the unmasking of yellow colour. Chlorophyll levels were restored upon regreening. Degreening coincided with the complete dismantling of the thylakoid system, while keeping the outer plastid envelope intact. Regreening resulted from the complete redifferentiation of these gerontoplast-like plastids into functional chloroplasts. The colour change was directly linked to the development of the inflorescence. Complete removal of the inflorescence before flowering prevented the colour change while removal at full bloom, when involucral leaves were yellow, resulted in significantly faster regreening. This designates the inflorescence or florets as the possible origin of the colour change trigger and suggests that the colour change is involved with attraction of pollinators. Degreening and regreening also took place in a growth chamber under continuous high light intensity. Therefore neither pollination nor the presence of roots is required for regreening. It appears that colour change in Leucadendron results from a well-regulated degradation and subsequent synthesis of photosynthetic pigments.

Environmental Influence on the Tolerance of Corn to Atrazine

Weed Science ◽  
1970 ◽  
Vol 18 (4) ◽  
pp. 509-514 ◽  
Author(s):  
Lafayette Thompson ◽  
F. W. Slife ◽  
H. S. Butler
Keyword(s):  
Zea Mays ◽  
High Temperature ◽  
Low Temperature ◽  
Light Intensity ◽  
Environmental Influence ◽  
High Light Intensity ◽  
High Light ◽  
Growth Chamber ◽  
Peptide Conjugates ◽  
Before And After

Corn(Zea maysL.) in the two to three-leaf stage grown 18 to 21 days in a growth chamber under cold, wet conditions was injured by postemergence application of 2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine (atrazine) plus emulsifiable phytobland oil. Injury was most severe when these plants were kept under cold, wet conditions for 48 hr after the herbicidal spray was applied, followed by exposure to high light intensity and high temperature. Under these growth chamber conditions, approximately 50% of the atrazine-treated plants died. Since wet foliage before and after application increased foliar penetration and low temperature decreased the rate of detoxication to peptide conjugates, atrazine accumulated under cold, wet conditions. This accumulation of foliarly-absorbed atrazine and the “weakened” conditions of the plants grown under the stress conditions is believed to be responsible for the injury to corn. Hydroxylation and the dihydroxybenzoxazin-3-one content in the roots were reduced at low temperature, but it is unlikely that this contributed to the death of the corn.

scholarly journals Effect of High Light Intensity Bleaching Protocol versus Descending Light Intensities Bleaching Protocol on Post Bleaching Teeth Sensitivity: A Randomized Clinical Trial

2019 ◽  
Vol 7 (13) ◽  
pp. 2173-2181
Author(s):  
Shadwa H. Kabil ◽  
Mohamed F. Haridy ◽  
Mohamed R. Farid
Keyword(s):  
Light Intensity ◽  
Colour Change ◽  
High Light Intensity ◽  
High Light ◽  
Parametric Test ◽  
Whitney Test ◽  
Anterior Teeth ◽  
Mann Whitney Test ◽  
Light Intensities ◽  
Shade Guide

AIM: The study aimed to compare teeth sensitivity and shade after bleaching protocol with descending different light intensities versus bleaching protocol with the same high light intensity. MATERIAL AND METHODS: Sample size was twenty-four patients. Each group consisted of twelve patients. Group, I patients received bleaching protocol of descending different light intensities. Group II patients received bleaching protocol with the same high light intensity; both groups used the same home bleaching gel kit for seven days according to manufacturer instructions and protocol. Baseline records were digital photographs, teeth sensitivity and teeth shade for 12 anterior teeth. Teeth sensitivity was assessed using five points verbal rating scale and Standardized 100 mm Visual analogue scale after 1 day, after 2 days and after 1 week. Teeth shades for twelve anterior teeth were recorded by VITA Easy Shade V (VITA Zahnfabrik H. Rauter GmbH & Co. KG, Germany) after 1 week by VITA Easy Shade V. Mann-Whitney test (non-parametric test, 2 independent samples) was used to compare teeth sensitivity between both bleaching protocols at each period. A paired t-test (parametric test, 2 related samples) was performed to compare the colour change in shade guide units (SGU) and ∆E values within high light intensity bleaching protocol. While Wilcoxon Signed-Rank test (non-parametric test, 2 related samples) was used to compare colour change light intensities bleaching protocol. Comparison of bleaching effectiveness (∆SGU and ∆Ediff) between both bleaching protocols was performed by the Mann-Whitney test. RESULTS: Descending light intensities protocol showed a lower teeth sensitivity than high light intensity protocol after 1 and 2 days. There was no teeth sensitivity reported at 1-week post-bleaching. Regarding the teeth shade, descending light intensities protocol had a little higher effect on colour change in shade guide units (SGU) than high light intensity protocol effect. Both bleaching protocols showed there was no significant difference in ∆SGU recorded after bleaching between high and descending light intensities protocols. CONCLUSION: Descending different light intensities protocol showed a lower teeth sensitivity than high same light intensity protocol. Descending light intensities protocol had a little higher effect on colour change in shade guide units (SGU) than high light intensity protocol effect.

Characteristics of Photosynthesis in Different Wheat Cultivars under High Light Intensity and High Temperature Stresses

2009 ◽  
Vol 34 (12) ◽  
pp. 2196-2201 ◽  
Author(s):  
Xue-Li QI ◽  
Lin HU ◽  
Hai-Bin DONG ◽  
Lei ZHANG ◽  
Gen-Song WANG ◽  
...  
Keyword(s):  
High Temperature ◽  
Light Intensity ◽  
High Light Intensity ◽  
High Light ◽  
Wheat Cultivars ◽  
Temperature Stresses

High light intensity stress as the limiting factor in micropropagation of sugar maple (Acer saccharum Marsh.)

2017 ◽  
Vol 129 (2) ◽  
pp. 209-221 ◽  
Author(s):  
Amritpal S. Singh ◽  
A. Maxwell P. Jones ◽  
Mukund R. Shukla ◽  
Praveen K. Saxena
Keyword(s):  
Light Intensity ◽  
Acer Saccharum ◽  
Sugar Maple ◽  
High Light Intensity ◽  
High Light ◽  
Limiting Factor ◽  
Intensity Stress

Predator Detection is Limited in Microhabitats with High Light Intensity: An Experiment with Brown-Headed Cowbirds

Ethology ◽  
2012 ◽  
Vol 118 (4) ◽  
pp. 341-350 ◽  
Author(s):  
Esteban Fernández-Juricic ◽  
Marcella Deisher ◽  
Amy C. Stark ◽  
Jacquelyn Randolet
Keyword(s):  
Light Intensity ◽  
High Light Intensity ◽  
High Light ◽  
Predator Detection

scholarly journals Effects of alkalinity and salinity at low and high light intensity on hydrogen isotope fractionation of long-chain alkenones produced by <i>Emiliania huxleyi</i>

2017 ◽  
Vol 14 (24) ◽  
pp. 5693-5704 ◽  
Author(s):  
Gabriella M. Weiss ◽  
Eva Y. Pfannerstill ◽  
Stefan Schouten ◽  
Jaap S. Sinninghe Damsté ◽  
Marcel T. J. van der Meer
Keyword(s):  
Light Intensity ◽  
Environmental Conditions ◽  
Hydrogen Isotope ◽  
Isotope Fractionation ◽  
Emiliania Huxleyi ◽  
High Light Intensity ◽  
High Light ◽  
Light Conditions ◽  
Low Light ◽  
Long Chain

Abstract. Over the last decade, hydrogen isotopes of long-chain alkenones have been shown to be a promising proxy for reconstructing paleo sea surface salinity due to a strong hydrogen isotope fractionation response to salinity across different environmental conditions. However, to date, the decoupling of the effects of alkalinity and salinity, parameters that co-vary in the surface ocean, on hydrogen isotope fractionation of alkenones has not been assessed. Furthermore, as the alkenone-producing haptophyte, Emiliania huxleyi, is known to grow in large blooms under high light intensities, the effect of salinity on hydrogen isotope fractionation under these high irradiances is important to constrain before using δDC37 to reconstruct paleosalinity. Batch cultures of the marine haptophyte E. huxleyi strain CCMP 1516 were grown to investigate the hydrogen isotope fractionation response to salinity at high light intensity and independently assess the effects of salinity and alkalinity under low-light conditions. Our results suggest that alkalinity does not significantly influence hydrogen isotope fractionation of alkenones, but salinity does have a strong effect. Additionally, no significant difference was observed between the fractionation responses to salinity recorded in alkenones grown under both high- and low-light conditions. Comparison with previous studies suggests that the fractionation response to salinity in culture is similar under different environmental conditions, strengthening the use of hydrogen isotope fractionation as a paleosalinity proxy.

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