Impact of ultraviolet radiation on cell structure, UV-absorbing compounds, photosynthesis, DNA damage, and germination in zoospores of Arctic Saccorhiza dermatodea

Stratospheric ozone depletion leads to enhanced UV-B radiation. Therefore, the capacity of reproductive cells to cope with different spectral irradiance was investigated in the laboratory. Zoospores of the upper sublittoral kelp Saccorhiza dermatodea were exposed to varying fluence of spectral irradiance consisting of photosynthetically active radiation (PAR, 400-700 nm; =P), PAR+UV-A radiation (UV-A, 320-400 nm; =PA), and PAR+UV-A+UV-B radiation (UV-B, 280-320 nm; =PAB). Structural changes, localization of phlorotannin-containing physodes, accumulation of UV-absorbing phlorotannins, and physiological responses of zoospores were measured after exposure treatments as well as after 2-6 d recovery in dim white light (8 mumol photon m(-2) s(-1)). Physodes increased in size under PAB treatment. Extrusion of phlorotannins into the medium and accumulation of physodes was induced not only under UVR treatment but also under PAR. UV-B radiation caused photodestruction indicated by a loss of pigmentation. Photosynthetic efficiency of spores was photoinhibited after 8 h exposure to 22 and 30 mumol photon m(-2) s(-1) of PAR, while supplement of UVR had a significant additional effect on photoinhibition. A relatively low recovery of photosystem II function was observed after 2 d recovery in spores exposed to 1.7 x 10(4) J m(-2) of UV-B, with a germination rate of only 49% of P treatment after 6 d recovery. The amount of UV-B-induced DNA damage measured as cyclobutane-pyrimidine dimers (CPDs) increased with the biologically effective UV-B dose (BED(DNA)). Significant removal of CPDs indicating repair of DNA damage was observed after 2 d in low white light. The protective function of phlorotannins has restricted efficiency for a single cell. Within a plume of zoospores, however, each cell can buffer each other and protect the lower layer of spores from excessive radiation. Exudation of phlorotannins into the water can also reduce the impact of UV-B radiation on UV-sensitive spores. The results of this study showed that the impact of UVR on reproductive cells can be mitigated by protective and repair mechanisms.     

Effects of UV-B radiation on ingestion, fecundity, population dynamics and antioxidant enzyme activities of Schmackeria inopinus (Copepoda Calanoida)

Effects of enhanced ultraviolet B (UV-B, 280-320 nm) on copepods have gained particular attention in recent years. In this study, we investigated the effects of UV-B radiation on ingestion, fecundity, population dynamics and antioxidant enzyme activities of copepod Schmackeria inopinus exposed to varying doses of UV-B irradiance. Artificial UV-B radiation resulted in an increased mortality of nauplii, copepodites and adults with increasing UV-B doses. Nauplii and copepodites were more sensitive to UV-B radiation than adults, and adult males had a higher UV-B radiation susceptivity in comparison with adult females. Both ingestion rates and proportion of gravid females decreased with the increase of UV-B doses; and at the same time, we also observed that adult females had higher ingestion rates as compared with adult males. In comparison with the control, the abundance of the treatment significantly decreased. Antioxidant enzyme (GPx and GR) activities attained a significant increase at lower UV-B radiation doses when compared to the control, but declined at higher UV-B doses. These results suggested that enhanced UV-B radiation might change the species composition of copepods. Our study also showed that antioxidant enzymes might protect S. inopinus against UV-induced oxidative damage.     

The sensitivity of Emiliania huxleyi (Prymnesiophyceae) to ultraviolet-b radiation

Emiliania huxleyi (Lohm.) Hay et Miller is an important component of the phytoplankton in open ocean waters. The sensitivity of this cosmopolitan alga to natural levels of UVB radiation has never been tested. Since DNA is believed to be a major target of natural UVB radiation (UVBR: 280–315 nm) in living cells, experiments with E. huxleyi were performed using growth rate reduction and DNA damage as indicators of UVBR stress. Specific growth rate, cell volume, pigment content, and CPD (cyclobutane pyrimidine dimer) formation (a measure for DNA damage) were followed during and after prolonged exposure of a series of cultures to a range of UVBR levels. E. huxleyi was found to be very sensitive to UVBR: at a daily weighted UVBR dose of only 400 J·m⁻² ·d⁻¹ (BED_DNA300nm), growth was halted. At this UVBR level, both cell volume and contents of the major photosynthetic and photoprotective pigments had increased. The UVBR vulnerability of E. huxleyi cannot be explained by a high potential for cyclobutane thymine dimer formation (the most abundant CPD type) due to a high T content of nuclear DNA: the CG content of this E. huxleyi strain is high (68%) compared with other species. The high UVBR sensitivity may be related to the stage of the cell cycle during UVBR exposure, in combination with low repair capacity. It is concluded that E. huxleyi may experience UVBR stress through the formation of cyclobutane pyrimidine dimers, with subsequent low repair capacity and thereby arrest of the cell cycle.     

UV damage to plant life in a photobiologically dynamic environment: the case of marine phytoplankton

The effect of UV-B radiation on growth of marine phytoplankton was investigated in relation to DNA damage induced by a range of biologically effective doses (BEDs). Emiliania huxleyi (Prymnesiophyceae) was chosen as a model organism of the ocean's phytoplankton because of its importance in global biogeochemical cycling of carbon and sulphur, elements that influence the world's climate as components of the trace gases carbon dioxide (CO₂) and dimethylsulfide (DMS). A marine diatom, Cyclotella, was studied for its capacity to repair the DNA damage, quantified as thymine dimers by the application of a monoclonal antibody against these photoproducts. DNA repair was shown to be complete after just a few hours of exposure to visible light; the repair rate increased with PAR intensity. E. huxleyi appeared to be most sensitive to UV-B radiation: growth was already affected above a dose of 100 J m^-2 d^-1 (biologically effective radiation, weighted with Setlow's DNA action spectrum), probably through effects on the cell cycle related to damage to nuclear DNA: mean specific growth rates were inversely correlated with thymine dimer contents in cells. Near the ocean's surface UV-B radiation conditions that induce the changes observed by us in cultures can be expected during the growing season of phytoplankton, not only in the tropics but also at higher latitudes. Nevertheles, blooms of species such as E. huxleyi are often excessive in the field. It is suggested that exposure duration of cells near the surface of the ocean can be shorter than our artificial 3 h in the laboratory due to vertical mixing, a phenomenon that is typical for the ocean's upper 50–100 m. When mixing reaches depths greater than the layer where most UV-B is attenuated, negative effects on cells through UV-A-induced inhibition of photosynthesis may prevail over DNA damage, the action spectrum of which has been shown to be limited to the UV-B part of the spectrum. Moreover, the radiation wavelengths that induce DNA damage repair (UV-A and visible) are attenuated vertically much less than UV-B. The photobiological situation in the upper ocean is much more complicated than on land, and effects of UV radiation on plankton biota can only be modelled realistically here when both the spectrally differential attenuation in the UV and visual part of the spectrum and the rate of vertical mixing are taken into account. Action spectra of both damage and repair of DNA and of photosynthesis inhibition of representative microalgal species are the second conditio sine qua non if we want to predict the effect of stratospheric ozone depletion on marine phytoplankton performance.     

Modification of leaf cytology and anatomy in Brassica napus grown under above ambient levels of supplemental UV-B radiation.

Plants exposed to natural solar radiation usually show acclimation responses on a daily and seasonal basis. Many of these responses are complex and modified by interactions with acclimation responses to other climatic factors. While changes in photosynthetically active radiation (PAR, 400-700 nm) are the driving force for many acclimation responses in plants, radiation outside the PAR range is also important. Recently, interest has increased in the potential role of UV-A (320-400 nm) and UV-B (280-320 nm) components of sunlight in plant developmental, physiological and daily acclimation processes. In order to explore the role of UV-B further, Brassica napus L. cv Paroll plants were grown to maturity under 13 kJ d(-1) of biologically effective ultraviolet-B radiation (UV-B(BE), 280-320 nm) plus 800 micromol photons m(-2) s(-1) photosynthetically active radiation (PAR, 400-700 nm) or PAR alone. Leaf anatomy and palisade cell structure were quantified using stereological techniques. The leaves of plants grown under UV-B radiation exhibited an increase in overall leaf width, although no change in leaf anatomy was discerned. Palisade cells in UV-B exposed leaves showed a significant decrease in chloroplast, mitochondrial, starch, and microbody volume density (Vv), while the vacuolar Vv increased compared to cells exposed to PAR only. In UV-B exposed leaves, there was an increase in the appressed and non-appressed thylakoid surface area density (Sv) within the chloroplasts. Since the relative proportion of appressed to non-appressed thylakoid surface area did not change, both thylakoid systems changed in concert with each other. Thylakoid stacks were broader and shorter in leaves subjected to UV-B. In general these responses were similar to those which occurred in plants moved from a high to low PAR environment and similar to mature plants exposed to 13 kJ d(-1) UV-B(BE) for only a short period of time. Although UV absorbing pigments increased by 21% in UV-B exposed leaves, there was no significant difference in chlorophyll a,b or carotenoid content compared to plants exposed to only PAR.     

UV tolerance in the two-spotted spider mite, Tetranychus urticae

The two-spotted spider mite, Tetranychus urticae was exposed to UV-C (250 nm), UV-B (300 nm), and UV-A (350 nm). In non-diapausing females, the median effective doses for 50% mortality plus escape incidence (ED₅₀) were 21 (UV-C) and 104 kJ m⁻² (UV-B); those for 50% oviposition rate in continuous darkness-treated mites were 6.2 (UV-C) and 41 kJ m⁻² (UV-B). No significant effects of UV-A on mortality and oviposition rate were observed. The ED₅₀ values for UV-B were similar to the natural UV-B observed for 2-5 days in summer when T. urticae inhabits the undersides of leaves. Therefore, T. urticae possibly uses leaves as a filter to avoid the deleterious effects of UV-B. In diapausing females, low mortality was observed even at high doses of UV radiation, but more than half escaped even at low doses. The orange body color of diapausing females results from accumulation of carotenoids, a scavenger for UV-induced reactive oxygen species; this may explain the low mortality of diapausing females. Diapausing females may overcome the deleterious effects of UV-B during winter in the absence of leaves by emigrating to UV-free environments and by accumulating carotenoids.     

Ingestion, faecal pellet and egg production rates of Calanus helgolandicus feeding coccolithophorid versus non-coccolithophorid diets

Ingestion rates, faecal pellet and egg production were obtained in laboratory experiments with females of the copepod Calanus helgolandicus collected from the English Channel in November 1994. Five different algal monocultures were used as food: Prorocentrum micans (30 μm ESD), Thalassiosira weissflogii (13 μm ESD), Dunaliella tertiolecta (7 μm ESD), Emiliania huxleyi (5 μm ESD) and Coccolithus pelagicus (14 μm ESD). Results obtained suggest the low ingestion efficiency of the copepod when feeding on coccolithophorids during late autumn-early winter. From the five species offered, only the largest non coccolithophorid Prorocentrum micans and Thalassiosira weissflogii supported efficient feeding and calculated respiratory demand for C. helgolandicus. Both coccolithophorids, irrespective of cell size, were ingested at very low rates even when offered at high concentrations (233-468 μg C l(-1)). Besides low ingestion, no egg production was found in the copepods fed with Emiliania huxleyi, although unusual high gross efficiency (reaching 72%) was obtained in experiments performed with Coccolithus pelagicus. The late seasonal timing of the experiments (November) could explain the low ingestion and egg production rates.     

Digitalis-like pregnanes. Cardiac and renal effects of a glycoside of 14 beta-hydroxyprogesterone

The synthesis of the glucoside, 3 beta-[(beta-D-glucopyranosyl)oxy]-14-hydroxy-14 beta-pregn-4-en-20-one, a 14 beta-hydroxyprogesterone glucoside (14 beta-OHP-glu), is described. This compound has an IC50 of 1 microM in a [3H]ouabain binding assay, and is about 10 times more potent than the aglycone. Like 14 beta-hydroxyprogesterone, the glucoside enhances contractility of isolated cardiac muscle. 14 beta-OHP-glu or ouabain, when infused at comparable doses into the renal artery of the anesthetized rat, markedly increases urine volume. Whereas ouabain significantly enhances urinary potassium excretion with little or no effect on sodium excretion, 14 beta-OHP-glu promotes a marked natriuresis with no significant effect on potassium excretion.     

Effects of UV-B radiation on embryonic, larval and juvenile stages of North Sea plaice (Pleuronectes platessa) under simulated ozone-hole conditions

Irradiation with artificial quasi-solar light was used to investigate lethal and sublethal effects of enhanced ultraviolet-B (UV-B) radiation on eggs, larval and juvenile stages of North Sea plaice. The irradiation experiments resembled a worst-case scenario with a synchronous occurrence of ozone depletion, sunny weather, and low water turbulence. In eggs, UV-B exposure increased mortality and induced loss of positive buoyancy. UV-B exposures for 1 or 2 days, according to the weather conditions in spring, impaired eggs only if UV-B intensities and doses exceeded those under a further 60% ozone loss. In larvae and juveniles, long-term UV-B exposures during and after metamorphosis affected ventilation rate at normoxia and ventilatory regulation during hypoxic incubations. Oxygen consumption rates of juveniles were not affected by UV-B irradiation. Received in revised form: 20 April 2000 Electronic Publication     

Impact of enhanced ultraviolet-B radiation on flower, pollen, and nectar production

Intensified ultraviolet-B radiation or UV-B (wavelengths between 280 and 320 nm) can delay flowering and diminish lifetime flower production in a few plants. Here we studied the effects of enhanced UV-B on floral traits crucial to pollination and pollinator reproduction. We observed simultaneous flowering responses of a new crop plant, Limnanthes alba (Limnathaceae), and a wildflower, Phacelia campanularia (Hydrophyllaceae), to five lifetime UV-B dosages ranging between 2.74 and 15.93 kJ·m·d. Floral traits known to link plant pollination with bee host preference, host fidelity and larval development were measured. Intensified UV-B had no overall effect on nectar and pollen production of L. alba and P. campanularia flowers. A quadratic relationship between UV-B and nectar sugar production occurred in P. campanularia and showed that even subambient UV-B dosages can be deleterious for a floral trait. Other floral responses to UV-B were more dramatic and idiosyncratic. As UV-B dosage increased, L. alba plants were less likely to flower, but suffered no delays in flowering or reductions to lifetime flower production for those that did flower. Conversely, an equal proportion of P. campanularia plants flowered under all UV-B treatments, but these same plants experienced delayed onset to bloom and produced fewer flowers at greater UV-B intensities. Therefore, intensified UV-B elicits idiosyncratic responses in flowering phenology and flower production from these two annual plants. Diurnal patterns in nectar and pollen production strongly coincided with fluctuating humidity and only weakly with UV-B dosage. Overall, our results indicated that intensified UV-B can alter some flowering traits that impinge upon plant competition for pollinator services, as well as plant and pollinator reproductive success.     

Ultraviolet-B radiation effects on the Mediterranean ruderal Dittrichia viscosa

Young seedlings of Dittrichia viscosa L. (syn. Inula viscosa (L.) Aiton) (Asteraceae) were extensively treated with artificial rain in order to remove the water soluble component of their epicuticular UV-B absorbing compounds. As a result, 75% of the epicuticular absorbing capacity at 300 nm was lost. The seedlings were subsequently grown in a naturaly lit glasshouse for 80 days under 0.06, 6.41 and 10.14 kJ m^-2 day ^-1 biologicaly effective UV-B radiation doses. The initial, pre-rain values of the water soluble, epicuticular UV-B absorbing potential was restored in about three weeks. During this transient period the plants were exposed to the enhanced UV-B radiation doses with part of their UV-B radiation screen removed. Although a trend for increased accumulation of epicuticular UV-B absorbing capacity was observed with increasing UV-B radiation doses, the allelopathic potential of the epicuticular material remained unchanged. Internal (cellular) UV-B absorbing compounds and chlorophylls were unaffected, but total carotenoids were increased, indicating a possible protective role against UV-B radiation damage. Leaf, stem and root dry mass were the same under all treatments but UV-B radiation caused a reduction in the dry mass invested per unit leaf area with a concomitant increase in leaf area. The importance of this UV-B radiation induced selective allocation of photosynthate to the production of assimilative surfaces is discussed.     

Rapid determination of spore chemistry using thermochemolysis gas chromatography-mass spectrometry and micro-Fourier transform infrared spectroscopy.

Spore chemistry is at the centre of investigations aimed at producing a proxy record of harmful ultraviolet radiation (UV-B) through time. A biochemical proxy is essential owing to an absence of long-term (century or more) instrumental records. Spore cell material contains UV-B absorbing compounds that appear to be synthesised in variable amounts dependent on the ambient UV-B flux. To facilitate these investigations we have developed a rapid method for detecting variations in spore chemistry using combined thermochemolysis gas chromatography-mass spectrometry and micro-Fourier transform infrared spectroscopy. Our method was tested using spores obtained from five populations of the tropical lycopsid Lycopodium cernuum growing across an altitudinal gradient (650-1981 m a.s.l.) in S.E. Asia with the assumption that they experienced a range of UV-B radiation doses. Thermochemolysis and subsequent pyrolysis liberated UV-B pigments (ferulic and para-coumaric acid) from the spores. All of the aromatic compounds liberated from spores by thermochemolysis and pyrolysis were active in UV-B protection. The various functional groups associated with UV-B protecting pigments were rapidly detected by micro-FTIR and included the aromatic C[double bond, length as m-dash]C absorption band which was exclusive to the pigments. We show increases in micro-FTIR aromatic absorption (1510 cm(-1)) with altitude that may reflect a chemical response to higher UV-B flux. Our results indicate that rapid chemical analyses of historical spore samples could provide a record ideally suited to investigations of a proxy for stratospheric O3 layer variability and UV-B flux over historical (century to millennia) timescales.     

Size and longevity of seed banks in Antarctica and the influence of ultraviolet-B radiation on survivorship, growth and pigment concentrations of Colobanthus quitensis seedlings

Populations of Colobanthus quitensis and Deschampsia antarctica, the only two vascular plant species native to Antarctica, are increasing. We performed a seed bank assay to determine the persistence of seeds from intact vegetation/soil cores collected near Palmer Station on the west coast of the Antarctic Peninsula. Vegetation/soil cores were cold stratified at 3 degrees C for >4 years. Subsequent seed bank densities, estimated from seedlings germinated, averaged 847 and 5645 seedlings m(-2) for C. quitensis and D. antarctica, respectively. We also conducted germination trials on C. quitensis seeds collected at our field site and stored for either 120 days or >4 years at 3 degrees C. Germination rates ranged from 6% after 120 days of cold storage to 38% after >4 years of cold storage. These findings show that previous estimates of seed bank densities and germination rates in these species, based on short-term laboratory stratification experiments, may underestimate those found in the field. Stratospheric ozone depletion has lead to increases in ultraviolet-B radiation (UV-B; 280-320 nm) along the Antarctic Peninsula during the austral spring. In a separate experiment we manipulated levels of biologically effective UV-B (UV-B(BE)), over current-year C. quitensis seedlings near Palmer Station on the west coast of the Antarctic Peninsula by placing frames over them that either held filters that absorbed most UV-B(BE) ('reduced UV-B(BE)'), transmitted most UV-B(BE) ('near-ambient UV-B(BE)') or had no filters ('ambient UV-B(BE)'). We monitored seedling survivorship over the course of the growing season (January-March) and growth and pigment concentrations at the end of the season. There were no UV-B(BE) treatment effects on seedling survivorship over the course of the season and overwinter survivorship averaged 12%. However, seedlings growing under near-ambient and ambient UV-B(BE) had 25 and 48% smaller total leaf areas, 7 and 16% fewer leaves and 65 and 82% fewer branches, respectively, than those growing under reduced UV-B(BE). In addition, concentrations of methanol-soluble UV-B-absorbing compounds were 26% higher and concentrations of chlorophyll b were 26% lower in leaves of seedlings growing under ambient UV-B(BE) compared with those under reduced UV-B(BE).     

Discovery of signaling effect of UV-B/C light in the extended UV-A/blue-type action spectra for step-down and step-up photophobic responses in the unicellular flagellate algaEuglena gracilis

Summary Cultures of unicellular algal flagellateEuglena gracilis grown in different conditions were subjected to action spectroscopy for step-down and step-up photophobic responses, respectively. The spectral region was extended into the UV-B/C as well as in the UV-A and visible regions with the Okazaki Large Spectrograph as the monochromatic light source. The photophobic responses of the cells were measured with an individual-cell assay method with the aid of a computerized video motion analyzer. In the UV-A and visible regions, the shapes of the action spectra were the so-called UV-A/blue type. In the newly studied UV-B/C region, new action peaks were found at 270 nm for the step-down response and at 280 nm for the step-up one. The absorption spectrum of flavin adenine dinucleotide (FAD) appeared to fit the action spectrum for the step-up response, whereas the shape of the step-down action spectrum, which has a UV-A peak (at 370 nm) higher than the blue peak (at 450 nm), appeared to be mimicked by the absorption spectrum of a mixed solution of 6-biopterin and FAD. These observations might also account for the fact that the UV-B/C peak wavelength at 270 nm of the action spectrum for the step-down response is shorter by 10 nm than the action spectrum for the step-up response at 280 nm.Abbreviations FAD flavin adenine dinucleotide - FWHM spectral full width at half maximum - NIBB National Institute for Basic Biology - OLS Okazaki Large Spectrograph - PFB paraflagellar body - UV-A ultraviolet light of spectral region between 320 and 400 nm - UV-B/C ultraviolet light of spectral region between 190 and 320 nm     

Evaluating UV-B effects and EDU protection in cucumber leaves using fluorescence images and fluorescence emission spectra

A newly developed laboratory fluorescence imaging system was used to obtain fluorescence images (FImage) of freshly excised cucumber (Cucumis sativus L.) leaves in spectral bands centered in the blue (F450), green (F550), red (F680), and far-red (F730) spectral regions that resulted from a broad-band (300-400 nm) excitation source centered at 360 nm. Means of relative fluorescence intensities (RFI) from these spectral fluorescence images were compared with spectral fluorescence emission data obtained from excitation wavelengths at 280 nm (280EX, 300-550 nm) and 380 nm (380EX, 400-800 nm) of dimethyl sulfoxide (DMSO) extracts from these leaves. All three fluorescence data types (FImage, 280EX, 380EX) were used to assess ultraviolet-B (UV-B, 280-320 nm) induced physiological changes and the possible use of N-[2-(2-oxo-1-imidazolidinyl) ethyl]-N′-phenylurea (EDU or ethylenediurea) as a chemical protectant against UV-B damage. Plants exhibited well known foliar growth and pigment responses to UV-B exposure (e.g., increased UV-B absorbing compounds and decreased leaf area, chlorophyll a content; and and lower chlorophyll a/b and chlorophyll/carotenoid pigment ratios). Since EDU alone had no effect on foliar variables, there was no evidence that EDU afforded protection against UV-B. Instead, EDU augmented some UV-B effects when provided in conjunction with UV-B irradiation (e.g., reductions in the chlorophyll/carotenoid ratio, total photosynthetic pigments, and chlorophyll b content).Relative fluorescence intensities (RFI) in the longer visible wavelengths (green, red, and far-red) were uncorrelated for comparisons between the FImage and 380EX data sets. However, blue and green RFI were significantly correlated (0.8r0.6; P ≤0.002) for comparisons between FImage and 280EX data sets. UV-B treatment caused an increase in blue RFI (e.g., F450) in both images and 280EX measurements. One explanation is that the UV-B excitation of both 280EX and FImage stimulates processes that produce excess blue fluorescence. The molecules that produce the excess blue fluorescence in both the 280EX and the Fimage data are different electron transfer agents that operate in parallel. For FImage, the UV excitation penetrates leaf surface layers to stimulate fluorescence from compounds in mesophyll and epidermal tissues (as occurs for the extracts of leaf discs), whereas emissions captured at longer, less energetic wavelengths, were primarily from the epidermal layer. UV-B irradiated leaves showed much greater heteorgeneity of RFI in both the green (F550_FImag) and the red (F680_FImag) bands than unirradiated leaves; this was true irrespective of EDU treatment.Although qualitative responses in individual bands differed between FImage and 380EX data, similar results were obtained in the detection of UV-B induced effects when the red/green and blue/far-red fluorescence ratios of these data were compared. The red/green ratio (either F680/F550_FImage or F675/F525_380EX) was lower for UV-B exposed plants in both images and 380EX data. UV-B exposure also significantly enhanced the blue/far-red ratio of images (F450/F740_FImage) and the comparable 380EX ratio (F450/F730_380EX) for the combined UV-B/EDU group. The far-red/red ratios were not useful in separating treatment effects in images or 380EX. Although comparable ratios were not available in 280EX data, the UV/blue ratio (F315/F420_280EX) was substantially reduced by UV-B exposure and was inversely related to total photosynthetic pigment content. These findings suggest that the red/green ratio (FImage, 380EX) and the UV/blue ratio (280EX) may be as useful as the blue/far-red ratio (380EX) reported previously in detection of UV-B stress. Furthermore, the results support the validity of the imaging technique as a non-destructive diagnostic tool for assessing UV-B stress damage in plants.     

UV-B辐射增强对海洋大型藻与微型藻种群生长关系的影响

选用孔石莼和青岛大扁藻为海洋大型藻和微型藻的代表,通过室内添加模拟试验研究了UV-B辐射增强对孔石莼(重量固定)与青岛大扁藻(密度不同)种群生长关系的影响。结果表明:(1)在单养情况下,4个UV-B辐射剂量都对孔石莼的生长产生抑制作用;对青岛大扁藻生长的影响却不同,低剂量(U-1)的UV-B辐射对青岛大扁藻的生长有促进作用,而高剂量的UV-B辐射则有显著的抑制作用;且因初始接种密度不同而各异。(2)在共养情况下,微藻对孔石莼的生长表现出一定的抑制作用,随着微藻初始接种密度的增加,其抑制作用亦增加;反之,在共培养的初始阶段(6 d内)孔石莼对微藻的生长也有抑制作用,但后期阶段(9 d后)表现出促进作用。(3)在共培养的同时附加UV-B辐射处理,随着初始接种密度的增加,青岛大扁藻对孔石莼生长的抑制作用更加明显;同时,与共养相比较,孔石莼对微藻生长的抑制作用亦趋于明显。     

Effects of UV-B on motility and photoorientation in the cyanobacterium,Phormidium uncinatum

UV-B irradiation has a detrimental effect on the survival of populations of the filamentous cyanobacterium, Phormidium uncinatum, at levels slightly higher than those currently measured at the surface of the earth. The organisms are not damaged or killed by UV-B radiation at 300 nm of 200 Wm^-2 for up to 20 h; but slightly increased levels of UV-B irradiation (2 h of 200 Wm^-2 at 300 nm) drastically impair motility, phototactic orientation and photophobic responses. These photosynthetic organisms require a narrow light intensity range for growth so that any decrease in their ability to actively search for and move into areas of favorable light conditions is bound to affect the survival of a population. The fluorescence yield of both phycobilins and chlorophyll is not altered even after 20 h of UV-B irradiation (200 Wm^-2 at 270 nm) indicating that UV-B at that dose does not affect the photosynthetic apparatus. The organisms are killed either by too bright intensities which bleach the photosynthetic pigments or by the lack of energy when they are unable to avoid moving into dark areas.     

Heat Shock Increases the Tolerance of Plants to UV-B Radiation: 1. Growth,Development, and Water Supply to Tissues

The effects of heat shock (HS); UV-B irradiation; and the consecutive action of these factors on the growth, development, and water supply of seven-day-old melon (Melo sativusSager., cv. Torpeda) seedlings were investigated. Depending on the HS severity, we observed growth stimulation (after treatment at 45°C for 1 h), growth retardation (after treatment at 45°C for 2 h or at 48°C for 1 h), or complete growth inhibition and cell death (after treatment at 45°C for 3 h or at 55°C for 1 h). UV-B irradiation (18.3 kJ/(m²h)), depending on its duration, stimulated (5–10 min), retarded (60 min), or resulted in complete growth inhibition and plant death (90 min). HS treatment (at 45°C for 1 h) prior to UV-B irradiation (for 1 h) favorably affected both the growth and water balance of seedlings. Apparently, the HS pretreatment increases the tolerance of seedlings to high doses of UV-B radiation.     

Photoproduction of dissolved inorganic carbon in temperate and tropical lakes – dependence on wavelength band and dissolved organic carbon concentration

We have evaluated photoeffects of UV-B, UV-A and PAR radiation on dissolved organic matter (DOM). Photochemical production of dissolved inorganic carbon (DIC) was measured in sterile lake water from Sweden and Brazil after 6 hours of sun exposure. Tubes were exposed to four solar radiation regimes: Full-radiation, Full-radiation minus UV-B, Full-radiation minus UV-B and UV-A (PAR) and darkness.In both areas, lakes with most DOC (varying between 3 and 40 mg C l^-1) were highly humic, resulting in high UV-B attenuation coefficients (K_d = 5–466 m^-1). Under Full-radiation, photooxidative DIC-production varied from 0.09 to 1.7 mg C l^-1per 6 h, without UV-B from 0.07 to 1.4 mg C l^-1 and with PAR only from 0.02 to 0.7 mg C l^-1. UV-B radiation explains a minor part (17%) of the photoooxidative DIC-production, while UV-A and PAR have larger effects (39% and 44%, respectively). Photooxidation was proportional to DOC-content and DIC-production was positively related to decrease in DOC and to loss of absorbance at 250 nm. There was no significant difference in DOC and radiation normalized DIC-production between Swedish and Brazilian lakes. The UV-B dose during incubations was approximately 3 times higher in Brazil compared to Sweden, while UV-A and PAR doses were similar. We conclude that DOC from tropical and temperate freshwaters do not seem to differ with respect to sensitivity to photooxidation.