Volatile metabolites and external CO2 exchange of wheat cenoses under optimal conditions and thermal stress

The effects of elevated temperature (35 and 45 degrees C) on photosynthesis, respiration, and both the qualitative and quantitative compositions of volatile emissions (VE) of wheat (Triticum aestuvum L. cultivar 232) cenoses at light intensities of 70, 150, or 240 W/m2 of photosynthetically available radiation (PAR) were studied. At a PAR of 240 W/m2, the thermal stabilities of photosynthesis and respiration increased at 35 degrees C and decreased at 45 degrees C. Elevated temperatures nonuniformly changed the rates and direction of VE syntheses. In this process, the highest increase in VE evolution was observed at 70 W/m2; the lowest, at 240 W/m2 and 35 degrees C. In addition, the concentrations and composition of VE during the repair period differed from the initial values.     

Characteristics of Slow Induction Curve of Chlorophyll Fluorescence and CO2 Exchange for the Assessment of Plant Heat Tolerance at Various Levels of Light Intensity

The heat tolerance of wheat (Triticum aestivum L.) and radish (Raphanus sativus L. var. minor) cenoses exposed to elevated and damaging air temperatures (35°C for 20 h, 45°C for 7 h) under photoculture conditions at various levels of photosynthetically active radiation (PAR) was assessed by measuring characteristics of the slow induction curve of chlorophyll fluorescence at 682 and 734 nm and the CO₂ exchange rate. Irrespective of the illumination level, the exposure of the cenoses to 35°C did not induce irreversible changes in the plant photosynthetic apparatus. The lowest extent of damage to wheat and radish cenoses exposed to 45°C was observed at 150 W/m² of PAR, whereas the highest damage of the plants was observed at an illumination level that was close to the compensation point of the cenose photosynthesis (50–70 W/m² of PAR at air temperature of 24°C). Viability index proved to be the most sensitive characteristic, compared to other characteristics, which were determined by measuring the slow phase of fluorescence induction at 682 and 734 nm. In the cenoses studied, the pattern of changes in the viability index in response to a stress factor was close to the changes in the photosynthetic rate.     

Moisture content and CO2 exchange of lichens

Summary Net photosynthesis (10 klx light intensity, 150 E m^-2 s^-1 PAR) and dark respiration of the lichen Ramalina maciformis at different temperatures are measured in relation to thallus water content. Both first increase with increasing hydration. Dark respiration then remains constant with increased water content until thallus saturation. In contrast, a further increase in water content leads to a depression of net photosynthesis, as shown in previous studies, after a maximum of CO₂ uptake has been attained. However, the extent of this depression depends strongly on temperature. In saturated thalli (160% water content in relation to lichen dry weight) the depression amounts to about 15% and 63% of the maximum unsaturated rate at 5°C and 25°C thallus temperature, respectively. The moisture compensation-point of net photosynthesis is also decisively determined by temperature (for 0°C at 20% water content; for 25°C at 15%), and the water content that allows maximum rates of CO₂ uptake (for 0°C at 80%; for 25°C at less than 40% water content). An electrical analogue of CO₂ exchange in a lichen thallus is presented, and it is suggested that the experimental results may be interpreted in terms of temperature-dependent CO₂ diffusion resistances in imbibed lichen thalli.     

Heat-Induced Increase in the Tolerance of the Wheat Photosynthetic Apparatus to Combined Action of High Temperature and Visible Light: CO2 Fixation,Photosynthetic Pigments,and Chloroplast Ultrastructure

Heating of the leaves of 15-day-old wheat (Triticum aestivum L.) plants at 42°C in the light (370 W/m² PAR) suppressed their ability to fix CO₂ twice stronger than heating in darkness. Heat hardening (3 h at 38–39°C) improved the tolerance of photosynthesis to combined action of high light and temperature but did not affect the tolerance to photoinhibition at 30°C. Hardening did not induce changes in the levels of photosynthetic pigments and their ratios. De-epoxidation of violaxanthin turned out to be more tolerant to photoinhibition at 42°C than CO₂ fixation. Protective effect of hardening was not related to the accumulation of zeaxanthin and activation of the xanthophyll cycle. Hardening protected the most sensitive population of chloroplasts against heat-induced photodamage and simultaneously increased the number and length of thylakoids. An increase in the volume of the thylakoid system was also induced by heating at 42°C and exposure to high light at 30°C. The formation of additional thylakoids and grana of shade type was not associated with improved tolerance of photosynthesis to heat and light stresses.     

Temperature and irradiance and the total daily photosynthetic production of the crown of a Pinus radiata tree

Summary Carbon dioxide exchange rates were recorded for different ages and positions of foliage and parts of the main stem of a 7-m tall Pinus radiata D. Don tree growing in a large, artificially lit, controlled-environment room. Irradiance levels were varied from dark to approximately full sunlight, and air temperatures from 10° to 35°C in 5°C steps. Leaf temperatures within the cuvettes used for CO₂ exchange measurements, however, were up to 5°C higher than the room air temperature set but this varied with position in the tree crown, the shaded lower crown being at approximately room temperature. A balance sheet was prepared to show the photosynthetic gains and respiratory losses of different parts of the crown over 24 h at each air temperature and at irradiances of 400, 270, and 135 W m^-2 during the 8-h photosynthetic period. The greatest daily photosynthetic gain was at 10° C, although this temperature is considered sub-optimal for growth. At temperatures greater than 25° C, even at the greatest irradiance level for 8 h, total respiration was greater than photosynthesis.     

Effect of Light Intensity, Carbon Dioxide Concentration, and Leaf Temperature on Gas Exchange of Spray Carnation Plants

The rates of CO₂ assimilation by potted spray carnation plants(cv. Cerise Royalette) were determined over a wide range oflight intensities (45–450 W m^–2 PAR), CO₂ concentrations(200–3100 vpm), and leaf temperatures (5–35 °C).Assimilation rates varied with these factors in a way similarto the response of single leaves of other temperate crops, althoughthe absolute values were lower. The optimal temperature forCO₂ assimilation was between 5 and 10 °C at 45 W m^–2PAR but it increased progressively with increasing light intensityand CO₂ concentration up to 27 °C at 450 W m^–2 PARand 3100 vpm CO₂ as expressed by the equation TOpt = –6.47-h 2.336 In G + 0.031951 where C is CO₂ concentration in vpmand I is photo-synthetically active radiation in W m^–2.CO₂ enrichment also increased stomatal resistance, especiallyat high light intensities. The influence of these results on optimalization of temperaturesand CO₂ concentrations for carnation crops subjected to dailylight variation, and the discrepancy between optimal temperaturesfor growth and net photosynthesis, are discussed briefly     

Pseudocyphellaria dissimilis: a desiccation-sensitive,highly shade-adapted lichen from New Zealand

Summary Pseudocyphellaria dissimilis, a foliose, cyanobacterial lichen, is shown not to fit into the normal ecological concept of lichens. This species is both extremely shade-tolerant and also more intolerant to drying than aquatic lichens previously thought to be the most desiccation-sensitive of lichens. Samples of P. dissimilis from a humid rain-forest site in New Zealand were transported in a moist state to Germany. Photosynthesis response curves were generated. The effect of desiccation was measured by comparing CO₂ exchange before and after a standard 20-h drying routine. Lichen thalli could be equilibrated at 15° C to relative humidities (RH) from 5% to almost 100%. Photosynthesis was saturated at a photosynthetically active radiation (PAR) level of 20 mol m^-2 s^-1 (350 bar CO₂) and PAR compensation was a very low 1 mol m^-2 s^-1. Photosynthesis did not saturate until 1500 bar CO₂. Net photosynthesis was relatively unaffected by temperature between 10° C and 30° C with upper compensation at over 40° C. Temporary depression of photosynthesis occurred after a drying period of 20 h with equilibration at 45–65% relative humidity (RH). Sustained damage occurred at 15–25% RH and many samples died after equilibration at 5–16% RH. Microclimate studies of the lichen habitat below the evergreen, broadleaf forest canopy revealed consistently low PAR (normally below 10–20 mol m^-2 s^-1) and high humidities (over 80% RH even during the day time). The species shows many features of an extremely deep shade-adapted plant including low PAR saturation and compensation, low photosynthetic and respiratory rates and low dry weight per unit area.     

Leaf photosynthetic characteristics of seedlings of actinorhizal Alnus spp. and Elaeagnus spp.

Single leaf photosynthetic characteristics of Alnus glutinosa, A. incana, A. rubra, Elaeagnus angustifolia, and E. umbellata seedlings conditioned to ambient sunlight in a glasshouse were assessed. Light saturation occurred between 930 and 1400 mol m^-2s^-1 PAR for all species. Maximum rates of net photosynthesis (Pn) measured at 25°C ranged from 12.8 to 17.3 mol CO₂m^-2s^-1 and rates of dark respiration ranged from 0.74 to 0.95 mol CO₂m^-2s^-1. These values of leaf photosynthetic variables are typical of early to midsuccessional species. The rate of Pn measured at optimal temperature (20°C) and 530mol m^-2s^-1 PAR was significantly (p<0.01) correlated with leaf nitrogen concentration (r=0.69) and negatively correlated with the mean area of a leaf (r=–0.64). We suggest that the high leaf nitrogen concentration and rate of Pn observed for Elaeagnus umbellata and to a lesser degree for E. angustifolia are genetic adaptations related to their crown architecture.Abbreviations Pn net photosynthesis     

Einfluß der Temperatur auf die Lichtatmung der Blaualge Anacystis nidulans

Summary CO₂ exchange, ¹⁴CO₂ fixation and ¹⁴C-products of Anacystis nidulans (strain L 1402-1) were studied during the induction period at temperatures of +15°C and+35°C. At+15°C the stationary rates of CO₂ uptake and respiration were reached directly. At+35°C a maximum of CO₂ uptake could be observed at the beginning of the illumination period followed by a lower steady rate of photosynthesis. In the following dark period a CO₂ gush appeared at+35°C. The magnitude of the CO₂ outburst is relatively independent of the photosyntbetic period. The autoradiographic studies showed that the Calvin cycle is the main carboxylation pathway in Anucystis. At a temperature of +35°C serine was labelled after 20 sec of photosynthesis. At+15°C, on the other hand, a low radio-activity appeared in serine after 5 min of photosynthesis. The results show that photorespiration of Anacystis is stimulated by high temperatures.     

Stem photosynthesis in Psorothamnus spinosus (smoke tree) in the Sonoran desert of California

Summary Stem photosynthetic responses to environmental parameters were investigated with Psorothamnus spinosus in the Sonoran Desert of California. Light saturation of stem photosynthesis was equal to maximum midday summer irradance (1600–2000 mol·m^-2·s^-1). The optimum temperature for stem photosynthesis was 39°C, and lower stem temperatures (27–35°C) caused significant decreases (up to 50%) in stem photosynthesis. Positive stem photosynthesis was maintained up to 51°C. Stem photosynthesis was relatively insensitive to increasing vpd up to 5 kPa; However, stem conductance decreased by 25% at a vpd of 5 kPa. At vpd greater than 5 kPa stem photosynthesis decreased relatively more than that of stem conductance causing a decrease in water use efficiency and an increase an intercellular carbon dioxide concentration. Maximum stem photosynthetic rates were low (6.2–10.6 mol·m^-2·s^-1) on a stem surface area, but, stem photosynthetic rates of young shoots were substantially higher (19.5–33.3 mol· m^-2·s^-1) on a projected area basis.Dedicated to the memory of Dr. W.H. Muller     

Effects of weather during leaf development on photosynthetic characteristics of soybean leaves

Net photosynthetic rates and mesophyll conductances at 25 °C at light saturation and air levels of carbon dioxide and oxygen were measured on recently fully expanded leaflets of second trifoliolate leaves of soybeans (Glycine max cv. Kent). Plants were grown outdoors in pots at Beltsville, Maryland with 14 planting times from May through August, 1983. Air temperature and humidity, and photosynthetically active radiation (PAR) were measured for the expansion periods of the second trifoliolate leaves. Rates of net photosynthesis ranged from 24 to 33 mol m^–2 s^–1, and mesophyll conductances from 0.24 to 0.35 cm s^–1 for the different planting dates. Mean 24-h air temperatures ranged from 20.6 to 29.0 °C, and mean daily PAR ranged from 29.4 to 58.4 mol m^–2 d^–1 for the leaf expansion periods. There was a positive relationship between photosynthetic characteristics and PAR during leaf expansion, and a negative relationship between photosynthetic characteristics and leaf expansion rates, with 96% of the variation in photosynthetic characteristics accounted for by these two variables. Leaf expansion rates were highly correlated with air temperature.     

Temperature-dependent feedback inhibition of photosynthesis in peanut

Arachis hypogaea L. is a tropical crop that is slow-growing at temperatures below 25°C. Unadapted CO₂-assimilation rate (A) showed insufficient variation between 15 and 30°C in the short term (hours) to explain this marked reduction in growth. However, at longer periods (12 d), A was depressed as were growth rate and leafproduction rate. To examine the possible relationship between growth, A and sink demand plants were transferred from 30°C, which is near the optimum for growth, to a suboptimal temperature (19°C). In the first 2 d of cooling, A decreased by 50–70%, the stomata stayed open, and the intercellular CO₂ concentration (c_i) rose, i.e. the decrease in A of the cooled plants was the result of non-stomatal factors. Changes in dark respiration did not account for the decline in A.Clear evidence was obtained of sink control of A by independently manipulating the temperature of different leaves on the plant. Cooling (to 19°C) most of the plant (the sink) led to a 70% decline in A of the remaining leaves at 30°C after 3 d, whereas the converse treatments (30°C sink, 19°C source) resulted in small changes (17%). In plants at 19°C which were exposed to low CO₂ concentration to prevent photosynthesis, A was not reduced when measured at normal CO₂ concentrations, indicating that carbohydrate accumulation was responsible for the decline in A. Dry-matter build-up at suboptimal temperature was also consistent with end-product inhibition of photosynthesis.Abbreviations and symbols A (mol·m^-2·s^-1) rate of net CO₂ assimilation - C_i (l·l^-1) substomatal CO₂ concentration - DW (g) dry weight - g (mol·m^-2·s^-1) stomatal conductance to diffusion of water vapour - PFD (mol·m^-2·s^-1) photon flux density     

Ecological and physiological investigations in continental Antarctic cryptogams

Summary Microclimate and CO₂ exchange of the lichen Usnea sphacelata were measured during summen on a hill near Casey Station, Bailey Peninsula, Wilkes Land, Antarctica. Within a period of 52 days (November 10 until December 31, 1985), 8 diurnal courses of net photosynthesis were measured in naturally snow-covered lichen thalli, and 9 diurnal courses in thalli experimentally sprayed with melt water. Photosynthetic performance of a light-form of Usnea sphacelata was compared with that of a shade-form. Net photosynthesis was reversibly depressed in snow-covered lichen thalli of both forms when irradiance was higher than 600 mol m^–2 s^–1 photosynthetic active radiation (PAR), the depression persisting several hours after a period of strong light. These responses suggest photoinhibition. Models of photosynthesis were established for the light-form by non-linear regressions with field data from water-sprayed thalli (Model W) and field data measured in snow-covered lichens (SNO I, SNO II). Model SNO I is based on median values of photosynthetic rates and SNO II on maximum values for each light/temperature combination. Photosynthetic rates were calculated using model W; the results showed values approximately three times higher than measured in the field with naturally moistened thalli. Photosynthetic rates according to model SNO II fitted the data of naturally moistened lichens measured during the day, before strong light (> 600 mol m^–2s^–1 PAR) caused reversible decrease of net photosynthesis. Model SNO I fitted the data measured during and after a phase of strong irradiance. Model SNO I demonstrated that light stress was highest at temperatures below 2 °C. This study has shown that long-term calculation of the photosynthetic productivity must take into account decreases in net photosynthesis rate caused by strong light, as well as effects of water content and temperature. For the investigated period of the austral summer, a carbon production of 3.44 gm^–2 was estimated for U. sphacelata.     

Inhibition of photosynthesis by chilling in moderate light: a comparison of plants sensitive and insensitive to chilling

Photosynthetic activity, in leaf slices and isolated thylakoids, was examined at 25° C after preincubation of the slices at either 25° C or 4° C at a moderate photon flux density (PFD) of 450 mol·m^–2·s^–1, or at 4° C in the dark. The plants used wereSpinacia oleracea L.,Cucumis sativus L. andNerium oleander L. which was acclimated to growth at 20° C or 45° C. The plants were grown at a PFD of 550 mol·m^–2·s^–1. Photosynthesis, measured as CO₂-dependent O₂ evolution, was not inhibited in leaf slices from any plant after preincubation at 25° C at a moderate PFD or at 4° C in the dark. However, exposure to 4° C at a moderate PFD induced an inhibition of CO₂-dependent O₂ evolution within 1 h inC. sativus, a chilling-sensitive plant, and in 45° C-grownN. oleander. The inhibition in these plants after 5 h reached 80% and 40%, respectively, and was independent of the CO₂ concentration but was reduced at O₂ concentrations of less than 3%. Methyl-viologen-dependent O₂ exchange in leaf slices from these plants was not inhibited. There was no photoxidation of chlorophyll, in isolated thylakoids, or any inhibition of electron transport at photosystem (PS)II, PSI or through both photosystems which would account for the inhibition of photosynthesis. The conditions which inhibit photosynthesis in chilling-sensitive plants do not cause inhibition inS. oleracea, a chilling-insensitive plant, or in 20° C-grownN. oleander. The CO₂-dependent photosynthesis, measured at 5° C, was reduced to about 3% of that recorded at 25° C in chilling-sensitive plants but only to about 30% in the chilling-insensitive plants. Methyl-viologen-dependent O₂ exchange, measured at 5° C, was greater than 25% of the activity at 25° C in all the plants. The results indicate that the mechanism of the chilling-induced inhibition of photosynthesis does not involve damage to PSII. That inhibition of photosynthesis is observed only in the chilling-sensitive plants indicates it is related, in some way, to the disproportionate decrease in photosynthetic activity in these plants at chilling temperatures.Abbreviations Chl chlorophyll - DPIPH reduced form of 2,6-dichlorophenol-indophenol - DMQ 2,5-dimethyl-p-benzoquinone - MV methyl viologen - 20°-oleander Nerium oleander grown at 20° C - 45°-oleander N. oleander grown at 45° C - PFD photon flux density (photon fluence rate) - PSI and PSII photosystem I and II, respectively     

Photosynthesis and water relations and the role of anatomy in Umbilicariaceae (lichenes) from Central Spain

Summary The response of net photosynthesis and dark respiration in eight species of Umbilicariaceae (lichenes) to temperature (-5, 0, 5, 10, 15, 20, 25, 30°C) and irradiance (55, 110, 220, 400, 620 mol photons m^-2 s^-1 PAR) was studied. The samples were collected in montane and alpine localities of the Spanish Sistema Central. The species differed widely in their net photosynthetic rates. The optimal temperature for net photosynthesis in alpine species was significantly lower than in montane species. Montane species were more photophytic than alpine ones. Water saturation and water loss rate were dependent on morphology and particularly anatomy of the thallus. The physiological and structural data are useful in the interpretation of the ecology and altitudinal distribution of the Umbilicariaceae. No adaptation could be linked to particularities of the mediterranean climate.     

Carbon dioxide exchange in Cladina lichens from subarctic and temperate habitats

Summary The survival potential of lichens in a given habitat is determined by the response of CO₂ exchange to photosynthetically active radiation (PhAR), thallus temperature, and thallus relative water content (RWC). Therefore morphologically similar lichens from contrasting climatic environments 1) should differ in their CO₂ exchange responses, and 2) these differences should reflect adaptations to their climatic regimes. The CO₂ exchange responses of a subarctic (55°N, 67°W) Cladina stellaris (Opiz) Brodo population and a temperate (29°N, 82°W) Cladina evansii (Abb.) Hale and W. Culb, population were used to test these two related hypotheses.Infrared gas analysis with lichens collected in September–October 1975 established that the two populations differed in their responses to incident PhAR, thallus temperature, and thallus RWC. Net photosynthesis in C. stellaris had an optimum at a lower temperature and a greater relative photosynthetic capacity at low temperatures than did C. evansii. Cladina evansii maintained net photosynthesis above 35°C thallus temperature; C. stellaris did not. In both species the optimum temperature for net photosynthesis increased with increasing irradiance. The C. stellaris light saturation point was consistently lower than that of C. evansii. Both species had maximal rates of net photosynthesis at 70–80% relative water content. In C. evansii the CO₂ exchange rates, expressed as percentages of the maximum rate, declined more rapidly under suboptimal conditions. The absolute CO₂ exchange rates of C. evansii were greater than those of C. stellaris. At 20°C and 90–95% RWC, resaturation respiration occurred in both species and continued until 6–7 h after wetting.Contrasts in the temporal patterns of thallus condition at each collection site suggest that not all differences in the two response surfaces reflect climatic adaptation. The two populations appear well adapted to incident PhAR and thallus temperature regimes but the 70–80% RWC optimum for net photosynthesis common to both species is puzzling since their water regimes differ markedly. The overall adaptedness of the CO₂ exchange responses in the two species cannot be judged without a comprehensive quantitative analysis of carbon balance under differing climatic regimes.     

Structural and Functional Characteristics of Ajuga reptansPhotosynthesis under Cold Climate Conditions

Structural, functional, and biochemical characteristics of the photosynthetic apparatus of a nemoral herbaceous perennial plant Ajuga reptansL. inhabiting the middle taiga subzone were investigated. Plant leaves were characterized by a high content of green (3.1 mg/dm²) and yellow (0.64 mg/dm²) pigments and contained moderate-sized chloroplasts with grana consisting of ten thylakoids or more. The maximum rate of photosynthesis in summergreen leaves (5–8 mg CO₂/(dm²h)) was observed at 14–16°C under a saturating photosynthetically active radiation of 50 W/m². At 6–7°C, the rate of CO₂assimilation was reduced to 60–80% of the maximum one. The temperature optimum of photosynthesis was not constant and shifted by 2–6°C depending on the changes in the ambient temperature. Wintergreen leaves were capable of photosynthesis in late autumn after heavy freezes and in early spring after a long winter. The accumulation of soluble carbohydrates and free amino acids in leaves helps to maintain the functional activity of the photosynthetic apparatus.     

Effect of salinity on photosynthetic activity of Nodularia spumigena

The aim of the study was to determine the influence of total dissolvedsolids/salinity (mg L^-1 TDS) on photosynthetic activity of Nodularia spumigena strain 001E isolated from Lake Alexandrina, SouthAustralia, using photosynthesis-irradiance (PI) curves. N. spumigena001E cultures were grown in ASM medium at a range of TDSconcentrations (360, 6,600, 13,200, 19,800, 26,400 mg L^-1)at an irradiance of 30 mol m^-2 s^-1 (PAR, 400–700 nm) at 25 °C. The PI relationship was determined at 25 °Cfor irradiances between 0 and 500 mol photon m^-2s^-1 (PAR). The initial slope of PI curve, , a function of lightharvesting efficiency and photosynthetic energy conversion, decreasedproportionally with an increase in salinity from 360 to 26,400 mgL^-1 TDS. The maximum rate of photosynthesis (P_max),occurred at 6,600 mg L^-1 TDS. No influence of salinity onI_k, the irradiance at which P_max was measured, or on R_d, the dark respiration rate, was identified.     

Photosynthesis and water-use characteristics in Indian mangroves

Photosynthesis and water efflux were measured in different PAR and stomatal conductance in members of Avicenniaceae and Rhizophoraceae. Trend of leaf temperature with irradiance and its effect on photosynthesis were also estimated. In most of the studied species, photosynthesis and stomatal conductance followed similar trends with increase in irradiance. The rate of net photosynthesis and stomatal conductance were higher in members of Avicenniaceae than in Rhizophoraceae. In Avicenniaceae, the optimum PAR for maximum photosynthesis ranged between 1340–1685 (μmol m^-2s^-1, which was also higher than that of Rhizophoraceae (840-1557 μmol m^-2s^-1). Almost in all the studied taxa, transpiration and stomatal conductance followed similar trends and reached the maximal peaks at the same PAR value. The range of breakeven leaf temperature was almost the same in both the families (34-36°C in Avicenniaceae and 33.5-36.3°C in Rhizophoraceae), beyond which assimilation rate declined.     

Effects of temperature and solar radiation interactions on the survival of quiescent conidia of the entomopathogenic hyphomycetePaecilomyces fumosoroseus (Wize) Brown and Smith

The detrimental effect of solar radiation on the survival of conidia of the entomopathogenic fungusPaecilomyces fumoroseus was studied by monitoring germinability and ability to form colonies (CFU) of conidia irradiated at two temperatures, 25 and 35 °C, harmless to shaded conidia. There was no apparent effect when spores were exposed to a high level of artificial radiation (0.66 W m^–2 UVB). However, at a lower level of irradiance (0.33 W m^–2), effects of radiation occurred more quickly at 35 °C than at 25 °C. Under natural solar radiation, the rate of decrease in germinability or viability was doubled at 35 °C as compared to 25 °C, indicating an interaction between temperature and radiation effects under natural conditions. This interaction was not detected in indoor experiments, indicating that the spectral distribution of UV radiation has to be taken in account as well as its irradiance when studying its effects.Abbreviations CFU Colony Forming Units - UTC Universal Time Coordinates - UVB Ultra Violet B radiation (280–320 nm)