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International audience; Microbial food spoilage is an important cause of health and economic issues and can occur via resilient contamination of food surfaces. Novel technologies, such as the use of visible light, have seen the light of day to overcome the drawbacks associated with surface disinfection treatments. However, most studies report that photo-inactivation of microorganisms with visible light requires long time treatments. In the present study, a novel light electroluminescent diode (LED)-based device was designed to generate irradiation at an ultra-high power density (901.1 mW/cm2). The efficacy of this technology was investigated with the inactivation of the yeast S. cerevisiae. Short-time treatments (below 10 min) at 405 nm induced a ~4.5 log reduction rate of the cultivable yeast population. The rate of inactivation was positively correlated to the overall energy received by the sample and, at a similar energy, to the power density dispatched by the lamp. A successful disinfection of several food contact surfaces (stainless steel, glass, polypropylene, polyethylene) was achieved as S. cerevisiae was completely inactivated within 5 min of treatments. The disinfection of stainless steel was particularly effective with a complete inactivation of the yeast after 2 min of treatment. This ultra-high irradiance technology could represent a novel cost- and time-effective candidate for microbial inactivation of food surfaces. These treatments could see applications beyond the food industry, in segments such as healthcare or public transport. KEY POINTS : • A novel LED-based device was designed to emit ultra-high irradiance blue light • Short time treatments induced high rate of inhibition of S. cerevisiae • Multiple food contact surfaces were entirely disinfected with 5-min treatments.

West sides of the coral Coelastrea aspera, which had achieved thermo-tolerance after previous experience of high solar irradiance in the field, were rotated through 180o on a reef flat in Phuket, Thailand (7o50´N, 98o25.5´E), in 2000 in a manipulation experiment and secured in this position. In 2010, elevated sea temperatures caused extreme bleaching in these corals, with former west sides of colonies (now facing east) retaining four times higher symbiont densities than the east sides of control colonies, which had not been rotated and which had been subject to a lower irradiance environment than west sides throughout their lifetime. The reduced bleaching susceptibility of the former west sides in 2010, compared to handling controls, suggests that the rotated corals had retained a ‘memory’ of their previous high irradiance history despite living under lower irradiance for 10 years. Such long-term retention of an environmental ‘memory’ raises important questions about the acclimatisation potential of reef corals in a changing climate and the mechanisms by which it is achieved.

When this Article was originally published, an old version of the associated Supplementary Information file was uploaded. This has now been replaced.

Rates of progression and transmission of black band disease (BBD) on the staghorn coral, Acropora muricata, were compared between months for seasonal in situ studies and between temperature treatments in experimental aquaria manipulations at Lizard Island on the Great Barrier Reef (GBR). In situ field experiments demonstrated that BBD progressed along branches approximately twice as fast (1.7–2.4 times) during the austral summer month of January (0.99 ± 0.04 cm/day) than in the cooler months of July (0.58 ± 0.04 cm/day) and May (0.41 ± 0.07 cm/day). Transmission of BBD between colonies was also accelerated in warmer months, with signs of infection becoming visible 1.2 days earlier in January compared to May. The greater seawater temperatures by ∼2 to 3°C and light intensities by up to 650 μE/m2/s in January, suggest that rates of progression and transmission of BBD are linked to one or both of these parameters. Manipulative experiments in summer provide corroborative evidence that elevated temperatures increase rates of BBD progression, with the disease progressing 1.3 times more rapidly in the 32°C elevated temperature treatment than in the 30°C ambient treatment (1.17 ± 0.06 cm/day versus 0.92 ± 0.07 cm/day; F2,6 = 7.66, P = 0.022). In contrast, although a trend for greatest BBD progression was measured in elevated temperature treatments of 29°C (0.46 ± 0.07 cm/day) and 31°C (0.52 ± 0.06 cm/day) in winter, these rates did not differ significantly (F3,7 = 1.72, P = 0.249) from those measured for the ambient 27°C treatment (0.37 ± 0.06 cm/day) or the field controls (0.41 ± 0.09 cm/day). The lower rates of BBD progression in the 31°C winter treatment (0.52 ± 0.06 cm/day) than in the 30°C (0.92 ± 0.07 cm/day) summer treatment, may have been a response to 28-fold decreased light irradiance in the former, suggesting that high irradiance in combination with elevated temperatures may promote progression of BBD. Results from this study indicate that the impact of elevated temperature on BBD progression is complex with a combination of environmental factors including temperature and light playing key roles in progression and transmission of the disease.

Laurencia brongniartii is usually found at depths below 4 m, but can be found in shallow subtidal areas in crevices and on the walls of a coral reef in Amami Oshima Island, Kagoshima Prefecture, Japan, where irradiances were significantly lower than those at similar depths in open water. In preparation for the possible cultivation of this species for its antibiotic compounds, the effects of temperature and irradiance on photosynthesis and growth were measured. Photosynthesis and growth rates of L. brongniartii explants were highest at 26 and 28 °C, which closely corresponded to temperatures found during August to late December when it was most abundant. The estimated maximum photosynthesis rate (Pmax) was 4.41 μmol photon m−2 s−1 at 26 °C and 4.07 μmol photon m−2 s−1 at 28 °C. Saturating irradiance occurred at 95 μmol photon m−2 s−1 at 26 °C and 65 μmol photon m−2 s−1 at 28 °C. In contrast, growth experiments at 41.7 μmol photon m−2 s−1 caused bleaching of explants and the maximum growth rate observed during the study was 3.02 ± 0.75% day−1 at 28 °C and 25 μmol photon m−2 s−1. The difference in the saturating irradiance for photosynthesis and the irradiance that caused bleaching in growth experiments suggests that long-term exposure to high irradiance was detrimental and should be addressed before the initiation of large scale cultivation.

Unicellular green algae of the genusDunaliella thrive in extreme environmental conditions such as high salinity, low pH, high irradiance and subzero temperatures. Species ofDunaliella are well known in the alga biotechnological industry and are employed widely for the production of valuable biochemicals, such as carotenoids. Some strains ofDunaliella are cultivated commercially in large outdoor ponds and are harvested to produce dry algal meals, such as polyunsaturated fatty acids and oils for the health food industry, and coloring agents for the food and cosmetic industries. During the past decade, the advances in molecular biology and biochemistry of microalgae, along with the advances in biotechnology of microalgal mass cultivation, enabled this microalga to become a staple of commercial exploitation. In particular, the advent of molecular biology and mutagenesis inDunaliella has permitted enhancements in the carotenoids content of this green alga, making it more attractive for biotechnological applications. Accordingly, the present review summarizes the recent developments and advances in biotechnology of carotenoid production inDunaliella.

Photoinhibition, defined as the inhibition of photosynthesis caused by excessive radiance, affects field production to a great extent. This phenomenon is particularly relevant in reforestation practices, when one deals with forests of rapid growth such asEucalyptus. The imposition of additional stress factors during exposure to high radiance increases the potential for photoinhibitory effects, so the inhibition of photosynthesis indicates that the plant is submitted to stressful conditions. Photoinhibition can be reversible, playing a protective role for the photosynthetic systems, but it can also reflect damage that has already occurred in the photosynthetic apparatus, being irreversible in this case. In this review, we present the physiological and molecular mechanisms of photoinhibition and discuss the interaction between light and other stress factors and its effects on plants destined for reforestation. In addition, the present work analyzes some of the features and strategies that help plants avoid or restrict the occurrence of photoinhibition. For instance, pigments and enzymes which naturally occur in plants can prevent photoinhibition, while preadaptation to nonideal conditions can enhance tolerance to a certain stress factor. Most of these morphological, metabolic, and biochemical mechanisms of defense are related to the dissipation of excessive energy such as heat. Understanding these mechanisms can help improve cultivation procedures, avoid the plants’ death, and increase productivity in the field.

The photoinhibition of photosynthesis was investigated on intact attached leaves and isolated thylakoid membranes of Populus deltoides.Our studies demonstrate that in intact leaves photoinhibition takes place under high irradiance which is more pronounced at higher temperatures. No net loss of Dl and other proteins associated with photosystem II (PSII) were observed even after 64 % photoinhibition suggesting that the degradation of polypeptides associated with PSII is not the only key step responsible for photoinhibition as observed by other workers. Electron transport studies in isolated thylakoid membranes suggested water oxidation complex as one of the damaged site during high light exposure. The possible mechanisms of photoinhibition without net loss of D1 protein are discussed.

The occurrence of very-low-fluence responses (VLFR), low-fluence responses (LFR) and high-irradiance responses (HIR) of phytochrome was investigated for the expression of the gene of β-glucuronidase (gusA) under the control of the tobacco Lhcb1*2 promoter, in etiolated transgenic tobacco seedlings. The activity of β-glucuronidase (GUS) showed biphasic responses to the calculated proportion of Pfr provided by light pulses. The first phase (i.e. the VLFR) showed a maximum for Pfr levels characteristic of far-red light. The second phase (i.e. the LFR) was observed at higher Pfr levels and was reversible by far-red light pulses. The strong effect of continuous far-red light (i.e. HIR) was fluence-rate-dependent and could not be replaced either by hourly pulses of the same spectral composition and total fluence or by very low fluences of red light. Deletion Lhcb1*2 promoter to -453 caused little loss of GUS activity. The -453 to -31, -270 to -31 and -176 to -31 fragments of the Lhcb1*2 promoter conferred proportionally normal VLFR, LFR and HIR to a truncated (-46 to +8) CaMV 35S minimal promoter. This is the first demonstration of the presence of three phytochrome action modes in the control of the transcriptional activity of a single gene. The cis-acting regulatory elements necessary for VLFR, LFR and HIR are present in a 146 bp fragment of the tobacco Lhcb1*2 promoter.

A recent noticeable climatic anomaly in some meteomarine quantities is analysed based on observations during the period March 1, 1971-February 28, 1993 taken in Trieste (Italy). Marked deviations from the normal values of the coupled quantities ‘atmospheric pressure-solar irradiance’ and ‘atmospheric pressure-sea level elevation’, during the last 22 years, are analysed. The procedures used bring out a clear and persistent configuration of high pressure, high irradiance and low sea level from 1989 on, previously unmatched.

Calcifying cyanobacteria from the Everglades, Florida, USA, have been cultured in the laboratory. Nutrient concentration of the culture medium and illumination are of special importance for filaments physiologically and morphologically similar to the forms occurring in the natural habitat. High irradiance leads to a good development of an inner, pigmented, uncalcified sheath layer. When the cyano-bacteria grow in water supersaturated with respect to calcite, the outer sheath layers can be impregnated by carbonate crystals. The internal diameter of the resulting tube, however, depends on the-environmentally controlled-thickness of the uncalcified inner sheath.

Plants growing in the natural environment are exposed daily to prolonged periods of high intensity irradiation. Many plant photomorphogenic responses are fully expressed only under prolonged exposures to high irradiances of light. The intensive study of these responses, the “High Irradiance Responses” (HIR) of plant photomorphogenesis, which started about 20 years ago, has been essentially directed—so far—toward the identification of the HIR photoreceptor, or photoreceptors, a problem that has not been satisfactorily and definitively solved, as yet. There is a great deal of evidence in support of the hypothesis that phytochrome, the pigment mediating the redfar red reversible plant photo-responses to low fluences of light, is involved in the photocontrol of the HIR. It seems likely that phytochrome may be the only photomorphogenic receptor responsible for the photocontrol of HIR responses brought about by irradiation at wavelengths longer than 600 nm. Phytochrome is probably also involved in the photocontrol of the HIR effects brought about by irradiation in the 350 to 500 nm region of the spectrum, but it cannot be excluded that other photochemical systems may also be involved. From a theoretical point of view, it does not seem unreasonable that the final expression of an HIR response may involve an interaction between phytochrome and other photochemical systems, with phytochrome probably playing the primary role and being responsible for the control of the activity of the other systems. Numerous “phytochrome only” interpretations (models) of the HIR have been proposed. Some of them have been developed to a fairly high degree of elaboration and have allowed the prediction of at least some of the features of the HIR. These “models,” although not rigorously and completely tested yet, seem to provide a reasonable interpretation for the HIR effects displayed under prolonged far red irradiation and for those HIR responses for which far red is the most effective spectral region. However, they do not provide a satisfactory explanation for the HIR responses for which blue is the most or the only effective spectral region, nor for the high effectiveness of white light. But, in spite of these problems, the “phytochrome only” interpretations of the HIR can be considered more satisfactory than those based on an interaction between phytochrome and other photochemical systems, especially in relation to the fact that the identity of these other photochemical systems has not been defined yet.

The characteristics of the 'high-irradiance response' (HIR) of plant photomorphogenesis are thought to be the result of the interaction of both the light and dark reactions of phytochrome. Thus any variation in the rates of the dark reactions may be expected to lead to variation in the characteristics of the HIR. We report here substantial differences in the rates of the dark reactions between different seed batches of a single species (Sinapis alba L.), and also between different organs of seedlings from each of the batches of seed. Calculations of phytochrome dynamics from the measured dark-reaction rates show that the behaviour of Pfr under HIR conditions will vary considerably according to seed batch and seedling organ. Much larger differences in dark-reaction rates, and the resulting phytochrome dynamics, were found between 25° and 10° C. These lead to the prediction that the HIR will be much reduced at the lower temperature, and may be absent in some cases.

Detailed action spectra are presented for the inhibition of hypocotyl extension in dark-grown Sinapis alba L. seedlings by continuous (24 h) narrow waveband monochromatic light between 336 nm and 783 nm. The results show four distinct wavebands of major inhibitory action; these are centred in the ultra-violet (λmax=367 nm), blue (λmax=446 nm), red (λmax=653 nm) and far-red (λmax=712 nm) wavebands. Previous irradiation of the plants with red light (which also decreases Ptot) causes decreased inhibitory action by all wavelengths except those responsible for the red light inhibitory response. Pre-irradiation did not alter the wavelength of the action maxima. It is concluded that ultra-violet and blue light act mainly on a photoreceptor which is different from phytochrome.