Absorption and utilization of radiant energy by light- and shade-adapted colonies of the hermatypic coral Stylophora pistillata

1984 ◽  
Vol 222 (1227) ◽  
pp. 203-214 ◽  

The specific absorption coefficient for chlorophyll a ( k c ) was measured in zooxanthellae from light- and shade-adapted colonies of the hermatypic coral, Stylophora pistillata from the Red Sea. These data, together with measurements of photosynthetic rates and irradiance, were used to compare the quantum yields of photosynthesis in these corals. Quantum yields varied from 0.10 CO 2 per quantum at low light to less than 0.001 CO 2 per quantum at maximal irradiances. Shade-adapted corals had higher pigment content, which allowed them to have twice as much light harvesting capability as light-adapted corals. In all cases, however, the quantum yield of the light-adapted corals was higher by a factor of about 1.5.

2015 ◽  
Vol 42 (12) ◽  
pp. 1168 ◽  
Author(s):  
Robert M. Cirocco ◽  
Melinda J. Waterman ◽  
Sharon A. Robinson ◽  
José M. Facelli ◽  
Jennifer R. Watling

Plants infected with hemiparasites often have lowered rates of photosynthesis, which could make them more susceptible to photodamage. However, it is also possible that infected plants increase their photoprotective capacity by changing their pigment content and/or engagement of the xanthophyll cycle. There are no published studies investigating infection effects on host pigment dynamics and how this relates to host susceptibility to photodamage whether in high (HL) or low light (LL). A glasshouse experiment was conducted where Leptospermum myrsinoides Schltdl. either uninfected or infected with Cassytha pubescens R.Br. was grown in HL or LL and pigment content of both host and parasite were assessed. Infection with C. pubescens significantly decreased all foliar pigment concentrations (except chlorophyll b) in L. myrsinoides in both HL and LL. Xanthophyll cycle (violaxanthin, antheraxanthin, zeaxanthin; VAZ) and chlorophyll (Chl) pigments decreased in parallel in response to infection, hence, VAZ/Chl of the host was unaffected by C. pubescens in either HL or LL. Pre-dawn and midday de-epoxidation state [(A + Z)/(V + A + Z)] of L. myrsinoides was also unaffected by infection in both HL and LL. Thus, L. myrsinoides infected with C. pubescens maintained similar photoprotective capacity per unit chlorophyll and engagement of the xanthophyll cycle as uninfected plants. Even though midday quantum yield (ΦPSII) of HL plants was affected by infection, pre-dawn maximum quantum yields (Fv/Fm) of hosts were the same as uninfected plants whether in HL or LL. This ability of L. myrsinoides to maintain photoprotective capacity/engagement when infected by C. pubescens thereby preventing photodamage could explain this host’s tolerance to hemiparasite infection.


1960 ◽  
Vol 38 (12) ◽  
pp. 2295-2302 ◽  
Author(s):  
Richard L. Stock ◽  
Harry E. Gunning

An investigation has been made of the reaction of cyclopentane with Hg 6(3P1) atoms at a substrate pressure of 107 mm, under static conditions at 24 °C. Low light intensities were used in order to minimize secondary reactions.The products of the reaction, for small extents of decomposition, have been shown to be exclusively hydrogen, bicyclopentyl, and cyclopentene. With increasing duration of exposure, the cyclopentene-to-cyclopentane ratio achieves a steady-state value of 5.7 × 10−3. Furthermore, it has been found that the same ratio is ultimately reached, upon prolonged exposure of a substrate initially containing cyclopentene at a concentration higher than the steady-state value. In the runs with added cyclopentene, a fourth product appeared in measurable quantities. Its molecular weight corresponded to the formula, C10H16, and it was assumed to be a cyclopentyl cyclopentene. The same compound appears in extensive decomposition of the pure substrate.The addition of small amounts of nitric oxide was found to have a marked inhibiting effect on the reaction. Bicyclopentyl formation was completely suppressed when 0.7 mole% of nitric oxide was present; and the cyclopentene yield was reduced to one-fifth of its value for the pure substrate, by adding 0.98 mole% of nitric oxide.In order to obtain primary quantum yields for the reaction, a series of runs were performed of 1 to 33 minutes in duration, with a cyclopentane which had been purified by gas–liquid chromatography. By a short extrapolation of the mean quantum yields of product formation to zero extent of reaction, it was found that the primary quantum yields for hydrogen, bicyclopentyl, and cyclopentene were respectively 0.8, 0.4, and 0.4.On the basis of a simple four-step paraffinic mechanism, taken in conjunction with the primary quantum yield data, it is concluded that the reaction has a primary quantum yield of substrate decomposition of 0.8, and that cyclopentyl radicals have the same rates for disproportionation and recombination at 24 °C.


2020 ◽  
Author(s):  
Wei Qiang Ong ◽  
C. Y. Maurice Cheung

AbstractConstraint-based modelling was applied to provide a mechanistic understanding of the possible metabolic origins of the ‘Kok effect’ – the change in quantum yield of net photosynthesis at low light intensity. The well-known change in quantum yield near the light-compensation point (LCP) was predicted as an emergent behaviour from a purely stoichiometric model. From our modelling results, we discovered another subtle change in quantum yield at a light intensity lower than the LCP. Our model predicted a series of changes in metabolic flux modes in central carbon metabolism associated with the changes in quantum yields. We demonstrated that the Kok effect can be explained by changes in metabolic flux modes between catabolism and photorespiration. Changes in RuBisCO carboxylation to oxygenation ratio resulted in a change in quantum yield at light intensities above the LCP, but not below the LCP, indicating the role of photorespiration in producing the Kok effect. Cellular energy demand was predicted to have no impact on the quantum yield. Our model showed that the Kok method vastly overestimates day respiration – the CO2 released by non-photorespiratory processes in illuminated leaves. The theoretical maximum quantum yield at low light intensity was higher than typical measured values, suggesting that leaf metabolism at low light may not be regulated to optimise for energetic efficiency. Our model predictions gave insights into the set of energetically optimal changes in flux modes in low light as light intensity increases from darkness.One sentence summaryThe Kok effect can be explained by the changes in flux modes between catabolism and photorespiration.


Author(s):  
Anja Busemann ◽  
Ingrid Flaspohler ◽  
Xue-Quan Zhou ◽  
Claudia Schmidt ◽  
Sina K. Goetzfried ◽  
...  

AbstractThe known ruthenium complex [Ru(tpy)(bpy)(Hmte)](PF6)2 ([1](PF6)2, where tpy = 2,2’:6’,2″-terpyridine, bpy = 2,2’-bipyridine, Hmte = 2-(methylthio)ethanol) is photosubstitutionally active but non-toxic to cancer cells even upon light irradiation. In this work, the two analogs complexes [Ru(tpy)(NN)(Hmte)](PF6)2, where NN = 3,3'-biisoquinoline (i-biq, [2](PF6)2) and di(isoquinolin-3-yl)amine (i-Hdiqa, [3](PF6)2), were synthesized and their photochemistry and phototoxicity evaluated to assess their suitability as photoactivated chemotherapy (PACT) agents. The increase of the aromatic surface of [2](PF6)2 and [3](PF6)2, compared to [1](PF6)2, leads to higher lipophilicity and higher cellular uptake for the former complexes. Such improved uptake is directly correlated to the cytotoxicity of these compounds in the dark: while [2](PF6)2 and [3](PF6)2 showed low EC50 values in human cancer cells, [1](PF6)2 is not cytotoxic due to poor cellular uptake. While stable in the dark, all complexes substituted the protecting thioether ligand upon light irradiation (520 nm), with the highest photosubstitution quantum yield found for [3](PF6)2 (Φ[3] = 0.070). Compounds [2](PF6)2 and [3](PF6)2 were found both more cytotoxic after light activation than in the dark, with a photo index of 4. Considering the very low singlet oxygen quantum yields of these compounds, and the lack of cytotoxicity of the photoreleased Hmte thioether ligand, it can be concluded that the toxicity observed after light activation is due to the photoreleased aqua complexes [Ru(tpy)(NN)(OH2)]2+, and thus that [2](PF6)2 and [3](PF6)2 are promising PACT candidates. Graphic abstract


Author(s):  
Panagiota Koralli ◽  
Spyridon Tsikalakis ◽  
Maria Goulielmaki ◽  
Stella Arelaki ◽  
Janina Müller ◽  
...  

Conjugated polymer nanoparticles (CPNs) have emerged as a new promising class of cancer theranostic agents due to their desirable optical features, such as high absorption coefficient and photoluminescence quantum yields,...


1981 ◽  
Vol 59 (11) ◽  
pp. 1607-1609 ◽  
Author(s):  
Karl R. Kopecky ◽  
Rodrigo Rico Gomez
Keyword(s):  

The quantum yields for photolysis of 0.25 M solutions of bicyclo[3.1.0]hexan-3-one, 1,5-dimethylbicyclo[3.1.0]hexan-3-one, and tricyclo[4.3.1.0]decan-8-one in pentane or cyclohexane with 313 nm light are 0.44, 0.52, and 0.32, respectively.


2021 ◽  
pp. 1-10
Author(s):  
Ibrahim Erden ◽  
Betül Karadoğan ◽  
Fatma Aytan Kılıçarslan ◽  
Göknur Yaşa Atmaca ◽  
Ali Erdoğmuş

This work describes the synthesis, spectral and fluorescence properties of bis 4-(4-formyl-2,6-dimethoxyphenoxy) substituted zinc (ZnPc) and magnesium (MgPc) phthalocyanines. The new compounds have been characterized by elemental analysis, UV-Vis, FT-IR, 1H-NMR and mass spectra. Afterward, the effects of including metal ion on the photophysicochemical properties of the complexes were studied in biocompatible solvent DMSO to analyze their potential to use as a photosensitizer in photodynamic therapy (PDT). The fluorescence and singlet oxygen quantum yields were calculated as 0.04–0.15 and 0.70–0.52 for ZnPc and MgPc, respectively. According to the results, MgPc has higher fluorescence quantum yield than ZnPc, while ZnPc has higher singlet oxygen quantum yield than MgPc. The results show that the synthesized complexes can have therapeutic outcomes for cancer treatment.


1999 ◽  
Vol 71 (2) ◽  
pp. 321-335 ◽  
Author(s):  
Angela Salinaro ◽  
Alexei V. Emeline ◽  
Jincai Zhao ◽  
Hisao Hidaka ◽  
Vladimir K. Ryabchuk ◽  
...  

In the preceding article [Serpone and Salinaro, Pure Appl. Chem., 71(2), 303-320 (1999)] we examined two principal features of heterogeneous photocatalysis that demanded scrutiny: (i) description of photocatalysis and (ii) description of process efficiencies. For the latter we proposed a protocol relative photonic efficiency which could subsequently be converted to quantum yields. A difficulty in expressing a quantum yield in heterogeneous photochemistry is the very nature of the system, either solid/liquid or solid/gas, which places severe restrictions on measurement of the photon flow absorbed by the light harvesting component, herein the photocatalyst TiO2, owing to non-negligible scattering by the particulates. It was imperative therefore to examine the extent of this problem. Extinction and absorption spectra of TiO2 dispersions were determined at low titania loadings by normal absorption spectroscopy and by an integrated sphere method, respectively, to assess the extent of light scattering. The method is compared to the one reported by Grela et al. [J. Phys. Chem., 100, 16940 (1996)] who used a polynomial extrapolation of the light scattered in the visible region into the UV region where TiO2 absorbs significantly. This extrapolation underestimates the scattering component present in the extinction spectra, and will no doubt affect the accuracy of the quantum yield data. Further, we report additional details in assessing limiting photonic efficiencies and quantum yields in heterogeneous photocatalysis.


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