Effect of column ozone on the variability of biologically effective UV radiation at high southern latitudes

Solar irradiance measurements from Ushuaia (Argentina) and Palmer and McMurdo Stations in Antarctica covering four seasons from mid-1993 through early 1997 have been analyzed and their variations compared with column ozone changes. UV irradiances were weighted for biological effectiveness using a published biological weighting function for dose-dependent inhibition of photosynthesis by phytoplankton from the Weddell Sea. All calculations involved integrated daily UV doses and visible exposures (weighted UV and unweighted visible irradiances, respectively). The results show that daily biologically effective total UV doses underwent large short-term variations at all three sites, with day-to-day increases up to 236% at Ushuaia, 285% at Palmer and 99% at McMurdo. Parallel changes in visible exposure indicated that the total UV changes were preponderantly due to variations in cloudiness. On a 12-month basis, daily biologically effective UV doses correlated strongly with visible exposures (R > or = 0.99). Anticorrelations of total UV with ozone, on the other hand, were poor (R > -0.11). The largest daily biologically effective UV doses, and their day-to-day increases, occurred as part of the normal variability related to cloud cover and were seldom associated with significant ozone depletion. UV dose/visible exposure ratios tended to reflect ozone depletion events somewhat more consistently than UV doses alone. With the Weddell Sea phytoplankton weighting function used in this study, antarctic ozone hole events were seldom readily discernible in the biologically effective UV record. The results suggest that, where the UV sensitivity of organisms was similar to that of the Weddell Sea phytoplankton, seasonal ozone depletion had no appreciable effect on annual primary productivity during the 1993-1997 period. Additional data on the geographical and seasonal variation of biological weighting functions are desirable for more comprehensive assessments of ozone depletion effects at high southern latitudes.     

Penetration of ultraviolet radiation in the marine environment. A review

UV radiation (UVR) is a significant ecological factor in the marine environment that can have important effects on planktonic organisms and dissolved organic matter (DOM). The penetration of UVR into the water column is likely to change in the near future due to interactions between global warming and ozone depletion. In this study we report underwater instruments employed for the measurement of UVR and we review data dealing with the depth of UVR penetration in different oceanic areas including the open ocean, Antarctic waters and coastal waters. We provide the 10% irradiance depth (Z10%) for UV-A and UV-B as well as for DNA damage effective dose (DNA), which we calculated from the values of diffuse attenuation coefficients or vertical profiles reported in the literature. We observe a clear distinction between open ocean (high Z10%, no variation in the ratio UV-B/UV-A), Antarctic waters (increase in the ratio UV-B/UV-A during ozone hole conditions) and coastal waters (low Z10%, no variation in the ratio UV-B/UV-A). These variations in the penetration of UVR could lead to differences in the relative importance of photobiological/photochemical processes. We also compare in this study the penetration of UV-B (unweighted and weighted by the Setlow action spectrum) and DNA damage effective dose.     

Ozone and UV radiation over southern South America: climatology and anomalies

Ozone and UV radiation were analyzed at eight stations from tropical to sub-Antarctic regions in South America. Ground UV irradiances were measured by multichannel radiometers as part of the Inter American Institute for Global Change Radiation network. The irradiance channels used for this study were centered at 305 nm (for UV-B measurements) and 340 nm (for UV-A measurements). Results were presented as daily maximum irradiances, as monthly averaged, daily integrated irradiances and as the ratio of 305 nm to 340 nm. These findings are the first to be based on a long time series of semispectral data from the southern region of South America. As expected, the UV-B channel and total column ozone varied with latitude. The pattern of the UV-A channel was more complex because of local atmospheric conditions. Total column ozone levels of < 220 Dobson Units were observed at all sites. Analysis of autocorrelations showed a larger persistence of total column ozone level than irradiance. A decreasing cross-correlation coefficient between 305 and 340 nm and an increasing cross-correlation coefficient between 305 nm and ozone were observed at higher latitudes, indicating that factors such as cloud cover tend to dominate at northern sites and that ozone levels tend to dominate at southern sites. These results highlight the value of long-term monitoring of radiation with multichannel radiometers to determine climatological data and evaluate the combination of factors affecting ground UV radiation.     

The effect of ultraviolet radiation on human viral infections

Exposure to UV radiation is recognized to suppress cell-mediated immunity and therefore could adversely affect the course of a viral infection. Rodent models of viral infection confirm this possibility but the situation in human subjects is not so clear, apart from two exceptions. These are herpes simplex, in which sunlight exposure can cause reactivation, and certain papillomavirus types in which sunlight exposure can lead to the development of nonmelanoma skin cancer. In both cases, there are UV response elements in the viral genomes that alter the normal interactions between the viruses and the host following exposure, and UV-induced effects on the immune response occur in addition. These complex mechanisms are discussed, and the situation regarding UV radiation and viral exanthems plus other viruses, including the retroviruses, summarized. Finally viral vaccination is considered in the context of UV exposure and the importance of the host's genetic background emphasized. Further research is required to evaluate whether sunlight can significantly affect the resistance to common viral infections and vaccines.     

The effect of ultraviolet radiation upon osmoregulation in Paramecium

Abstract Paramecium multimicronucleatum was irradiated with U.V. in solutions of differing osmotic pressures and ionic content. The rates of contraction and the diameters of the anterior contractile vacuoles were measured and changes in the volumes of solution entering the contractile vacuoles upon U.V. irradiation for paramecia maintained in solutions of differing ionic content were calculated. The volume of fluid entering the contractile vacuoles of paramecia irradiated (1) in standard balanced salt solution (SBSS) was regulated by a compensatory mechanism at lower U.V. doses but increased after relatively large U.V. doses; (2) in distilled water, increased after much smaller U.V. doses; (3) in isotonic balanced salt solution, showed little change upon irradiation. Increased osmotic pressure (with added sucrose) was found to reduce u.v.-induced blistering of the pellicle, but in general U.V. damage was similar to that of paramecia in solutions of identical ionic content but lacking sucrose. Paramecia in SBSS with added sucrose to make it isomotic to the interior of the cell ruptured only after doses larger than for paramecia in SBSS lacking sucrose. Cell rupture of paramecia in solutions containing high CaCl₂ concentrations generally occurred later than for those in SBSS. High KCI concentration (unbalanced salt solution) in the presence of high CaCl₂ concentration provided some protection from U.V. irradiation to the paramecia. High NaCl concentration (unbalanced salt solution) in the presence of high CaCl₂ concentration appeared to increase u.v. damage to paramecia. Paramecia were most resistant to u.v. irradiation, as judged by the above criteria, when present in balanced salt solution enriched with calcium, thus simulating pond water.     

Oxidation behaviour in prosthetic UHMWPE components sterilised with high energy radiation in a low-oxygen environment

Oxidation of the UHMWPE component during sterilisation with high energy radiation has been recognised as one of the main problems affecting the durability of orthopaedic implants. Oxidation is always present in radiation-sterilised polymeric components due to the oxygen diffused into UHMWPE. Hydroperoxides are the first products of the oxidation cycle and they are also a convenient species to follow for monitoring the oxidation. In the present study, the early stages of oxidation were investigated by assessing the hydroperoxide levels and distribution in a selection of ready-to-use UHMWPE prosthetic components. The samples included in the study were chosen from a larger group, according to the following criteria: they were packaged in a low-oxygen environment, radiation-sterilised and carbonyl free. FTIR spectroscopy and derivatisation techniques were used to characterize the hydroperoxide concentration and distribution. Hydroperoxides were detected in all samples, despite the sterilisation in inert atmosphere. Three different behaviours were identified and discussed and a correlation with the packaging and sterilisation conditions is proposed.     

The effect of environment on cystine disruption by ultraviolet light

When cystine is irradiated at pH 1 by 254-nm u.v. the following yields are observed: 4 cystines → 5.2 cysteines + 2.8NH₃. Thus, SH production accounts for only 0.65 of the cystine destruction; further C-S breakage to give alanine or serine is not efficient. The yields for cystine and glutathione destruction are essentially the same at pH 1. However the presence of the glutamic and glycine residues stabilize the cystine in glutathione so that NH₃ is not lost until the peptide bonds are hydrolyzed. Increasing the pH from 1 to 8.6 increases the yield of cystine destruction in glutathione by 50 per cent. The yield of cystine destruction is greater in both compounds when O₂ is present during irradiation (e. g. the cysteic acid yield in glutathione is increased by 50 times). The overall production of SH varies by a factor of 2 in the four proteins-insulin, RNase, trypsin and lysozyme. The present data further support the earlier observation that radiation damage is quite non-random in RNase: at least two and perhaps three of the four constituent cystines must be disrupted before activity is lost: i.e. the most radiosensitive cystines are not critical for enzymic activity. Similarly, in both trypsin and lysozyme the integrity of the most radiosensitive cystines also does not appear to be critical for the retention of enzymic potential. In insulin, however, all three cystines appear to be crucial for activity and to have approximately equal radiosensitivities. These differences in sensitivity of cystines in different proteins must depend specifically upon energy transfer and/or chemical interactions between the chromophoric groups. If yields are calculated on the basis of those quanta absorbed only in the cystines, values about 5 to 8 times greater than those in the model compounds cystine and oxixized glutathione are obtained. The yields of cystine destruction are much higher in those protiens which contain trypotophan.     

Photolysis of a fluorinated polymer film by vacuum ultraviolet radiation

We studied the photolysis of a fluoroethylene–fluoropropylene copolymer (FEP) film by vacuum ultraviolet (VUV) radiation from a resonance Xe lamp at a wavelength of 147 nm and air pressures of 0.05 and 2.5 Torr. The chemical changes in the FEP surface layer were investigated by Fourier-transform infrared spectroscopy with attenuated total reflection attachment and X-ray photoelectron spectroscopy. Double bonds were found to be the main product in the case of VUV treatment at 0.05 Torr, while photo-oxidation of FEP occurred predominantly by VUV treatment at 2.5 Torr under formation of the —CF₂C(O)F group. This oxygen-containing group was more effectively formed in the FEP surface layer by VUV photo-oxidation than by conventional surface oxidation techniques such as treatments by plasma and corona discharge and ozone. Storage of the VUV-treated polymers in air at 50% relative humidity resulted in hydrolysis of —CF₂C(O)F to the —CF₂COOH group. Substantial improvement of the film wettability was noticed after VUV photo-oxidation. These findings suggest that VUV irradiation provides a high potential for surface modification of fluorinated polymers which are known to be particularly resistant against functionalization by conventional surface modification techniques such as plasma treatment. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2215–2222, 1998     

Effect of ultraviolet radiation on a metal/polyamidine system

An increase in the optical transmission in electronic spectra for metal/poly(1,10-decamethylene-acetamidine) systems after UV irradiation is observed, in contrast to polymer and metal films investigated separately where there was no such effect. The increase is explained by changes in the distribution of the electric charge induced by UV irradiation at the metal/polymer interface in a polymer film.     

Inactivation of a Rhizobium bacteriophage by ultraviolet radiation of different wave-lengths

Abstract— Trypsin inactivated by u.v. radiation, gamma radiation, visible radiation in the presence of sensitizing dyes, and autolysis, was examined by the method of disc electrophoresis. Untreated Worthington twice crystallized salt-free trypsin separated into four bands which moved toward the cathode; the main band, which had the greatest mobility, contained all of the detectable tryptic activity. The next most mobile band has been assumed to be a chymotrypsin contaminant. The other two bands are of unknown nature. A progressive loss of all the bands was observed when the enzyme was inactivated by those procedures which produce a ‘damaged’ class of trypsin molecules, i.e. flavin-sensitized photooxidation, autolysis, and treatment with u.v. and gamma radiation. No loss of the main band was observed during photoinactivation with methylene blue and eosin Y as sensitizers. In this latter case, it is postulated that the trypsin inactivation products must be of such a nature that the net charge and conformation of the protein is not greatly changed, thus permitting all of the protein to remain in the same band during electrophoresis.     

The alkaloid brachycerine is induced by ultraviolet radiation and is a singlet oxygen quencher

The effects of ultraviolet (UV) radiation on chlorophyll content and accumulation of the anti-inflammatory monoterpene-indole alkaloid brachycerine in plants and calli of Psychotria brachyceras (Rubiaceae) were investigated. In this study, we also investigated a protective role for brachycerine against stress conditions. Calli and tip cuttings incubated in nutrient media were daily supplemented with 4 or 16 h of UV. High-performance liquid chromatography analyses of methanolic extracts showed only traces of brachycerine in irradiated aseptic cultures, with no alkaloid being observed in control calli. In cuttings, a 10-fold increase in brachycerine content was seen after exposure for 16 h to UV-C, whereas a 4 h daily supplementation doubled the amount of the alkaloid in leaves. Exposure to a UV-B source also doubled the alkaloid yield. In vitro brachycerine was able to quench singlet oxygen. The data indicate a potential protective role for brachycerine against UV radiation, acting as a UV filter (absorption peaks are within the UV range) and a reactive oxygen species scavenger. In addition, UV radiation may be used to increase yields of this compound of pharmaceutical interest.     

The effect of chronic ultraviolet radiation on the human immune system

A single or a limited number of UVR exposures is recognized to suppress cell-mediated immunity in human subjects. The complex pathway leading from the absorption of photons by chromophores in the skin to the generation of T regulatory cells has been, at least partially, elucidated. However, the effect of repeated UV exposures on immune responses and associated mediators is not well studied, particularly to assess whether they lead, first, to the development of photoprotection so that these immune changes are reduced or no longer occur, and, secondly, to the development of photoprotection against the normal downregulation of immunity induced by a high UV dose. For almost all the parameters evaluated in this review--epidermal DNA damage/erythema, urocanic acid, Langerhans and dendritic cells, natural killer cells, macrophages, mast cells, contact and delayed hypersensitivity responses--none, aside from epidermal DNA damage/erythema and macrophage phagocytic activity, show convincing evidence of photoadaptation or, where appropriate, photoprotection. It is concluded that repeatedly irradiating individuals with UVR is likely to continue to result in downregulation of immunity.     

Youth solar ultraviolet radiation exposure, concurrent activities and sun-protective practices: a review

To assist standardization of procedures, facilitate comparisons, and help guide research efforts to optimally inform development of appropriately targeted interventions, there is a need to review methods used to quantify child and adolescent solar ultraviolet radiation (UV) exposure, related outdoor activities and sun-protective practices. This holistic approach is essential for comprehensive research that will provide all-inclusive, informative and meaningful messages for preventive measures of harmful UV exposure. Two databases were searched and 29 studies were retrieved, and these studies report measurement or assessment techniques documenting UV exposure patterns and related outdoor activities. Polysulfone film badges were the main measurement instrument used in 10 studies, with questionnaire, survey data, observation, a model, electronic dosimeters, biological dosimeters, colorimeter and UV colouring labels used in the remaining studies. Methods used to record activities included self-report, parental report, a logbook and observation. Measurement duration and unit of UV exposure varied in most studies, but a method common to 15 studies was measured UV exposure as a percentage of ambient UV. The studies reviewed do not provide sufficient information for the development and evaluation of targeted youth sun protection programs. Studies are required which document precise UV exposure, concurrent activities and sun protection usage for children and adolescents.     

Gamma and ultraviolet radiation cause DNA crosslinking in the presence of metal ions at high pH.

M-DNA is a novel duplex conformation in which metal ions such as Co2+, Ni2+ or Zn2+ replace the imino protons of every base pair. An ethidium fluorescence assay was used to estimate lesions in M-DNA induced by gamma- and UV radiation. General damage to DNA was assessed from the loss of ethidium fluorescence after irradiation of calf thymus DNA. Crosslinks were measured from the return of ethidium fluorescence after a heating and cooling step. Strand breaks were estimated from the loss of fluorescence in covalently closed circular plasmid DNA after a heating and cooling step. For the Co2+ form of M-DNA, gamma-radiation caused the very efficient formation of crosslinks which was not observed with B-DNA nor with the Ni2+ or Zn2+ forms of M-DNA. The crosslinks occurred in both A-T and G-C base pairs but did not form in the presence of a free radical scavenger. Crosslinks induced by UV radiation also formed at a faster rate in the Co2+, Ni2+ and Zn2+ forms of M-DNA compared to B-DNA; crosslinking occurred in all DNA but was more prominent in AT-rich sequences and was not inhibited by a free radical scavenger. Therefore, the presence of certain metal ions may lead to large increases in the formation of radiation-induced crosslinks in DNA.     

Estimating attenuation of ultraviolet radiation in streams: field and laboratory methods

We adapted and tested a laboratory quantitative filter pad method and field-based microcosm method for estimating diffuse attenuation coefficients (K(d)) of ultraviolet radiation (UVR) for a wide range of stream optical environments (K(d320) = 3-44 m(-1)). Logistical difficulties of direct measurements of UVR attenuation have inhibited widespread monitoring of this important parameter in streams. Suspended sediment concentrations were manipulated in a microcosm, which was used to obtain direct measurements of diffuse attenuation. Dissolved and particulate absorption measurements of samples from the microcosm experiments were used to calibrate the laboratory method. Conditions sampled cover a range of suspended sediment (0-50 mg L(-1)) and dissolved organic carbon concentrations (1-4 mg L(-1)). We evaluated four models for precision and reproducibility in calculating particulate absorption and the optimal model was used in an empirical approach to estimate diffuse attenuation coefficients from total absorption coefficients. We field-tested the laboratory method by comparing laboratory-estimated and field-measured diffuse attenuation coefficients for seven sites on the main stem and 10 tributaries of the Lehigh River, eastern Pennsylvania, USA. The laboratory-based method described here affords widespread application, which will further our understanding of how stream optical environments vary spatially and temporally and consequently influence ecological processes in streams.     

Measurement of solar ultraviolet radiation at a temperate and a tropical site using polysulphone film

Measurements of solar ultraviolet radiation (<320 nm) have been made with polysulphone film at a temperate and a tropical site and compared mean monthly values of the fraction of ultraviolet in solar radiation are calculated which allow an estimate of ultraviolet dose to be made from a knowledge of total solar radiation.While the data demonstrate the marked effect of sun elevation on the ultraviolet fraction of solar radiation they also indicate the effect of seasonal variation in the thickness of the ozone layer above the temperate site.It is also shown that whereas sunlight makes by far the major contribution to total solar radiation, skylight is of prime importance as regards ultraviolet radiation.     

The induction of immunity to a protein antigen using an adjuvant is significantly compromised by ultraviolet A radiation

Ultraviolet (UV) radiation from sunlight causes skin cancer and inhibits priming of the immune system during vaccination. However the dose related effects of the different components of sunlight (UVA and UVB) are complex and require further investigation. Using ovalbumin as a model protein vaccine with saponin as adjuvant we show that both UVA and UVB can suppress the DTH response to a poorly immunogenic protein. Increasing doses of UVB induced increased levels of immunosuppression and tolerance. UVA however, caused a bi-phasic dose response with intermediate but not low or high doses causing primary immunosuppression. No dose of UVA caused significant tolerance. Similar results were observed in both C57BL/6 and Balb/c mice. Our data confirms the complex immunomodulatory dose effects of UVA and UVB for a protein antigen, and shows that both UVB and UVA can suppress immunity induced by a protein with adjuvant. This highlights the importance of considering sun exposure patterns in the future success of both preventing skin cancer development and enhancing vaccination regimes.     

The solidification behavior of a PBT/PET blend over a wide range of cooling rate

In recent years, much attention has been paid to the development of high‐performance polyester blends, among which blends of polybutylene terephthalate/polyethylene terephthalate (PBT/PET) are expected to exhibit remarkable properties as far as their crystallization behavior is concerned. Through trial and error, appropriate commercial compositions have been chosen which could not be otherwise explained by a suitable interpretation of the mechanisms determining their solidification behavior. The solidification behavior of a 60/40 w/w PBT/PET blend was studied in a wide range of cooling conditions, according to a continuous cooling transformation (CCT) procedure developed previously, aiming at emulating the typical conditions encountered in polymer processing. Several samples characterized by a homogeneous structure were solidified from the melt at various cooling rates and the resulting structure and properties were subsequently evaluated by analyzing the density, microhardness (MH), and wide angle x‐ray diffraction (WAXD). The resulting solidification behavior was then compared to that exhibited by the individual constituents of the blend (i.e., PBT and PET). The blend displayed a unique solidification behavior, conversely to those of the pure components which showed characteristics not recognized in the blend except at certain restricted cooling rates ranges. The cooling rate dependence observed in the blend does not bring similarities to the crystallization behavior of individual constituents since the fall down of density with cooling rate should be related to the rate controlling demixing stage of the two moieties just before crystallization occurs. The kinetics observed is thus a measure of the kinetics of demixing. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 799–810, 2009     

Early induction of binucleated cells by ultraviolet A (UVA) radiation: a possible role of microfilaments.

The effects of UVA (365 nm) radiation on the cellular distribution of F-actin and formation of binucleated cells have been studied using 3T3 Swiss albino mouse fibroblasts and V79 Chinese hamster fibroblasts. Ultraviolet A at biologically relevant fluences was found to disintegrate the actin filaments in the cells shortly (5 min) after irradiation, concomitant with the formation of cells with two nuclei. In 76-100% of the bi- and multinucleated cells the distribution of F-actin was clearly altered. Cells in GI phase of the cell cycle were most probably involved in the formation of binucleated cells. The disintegration of F-actin was presumably not due to depolymerization of F-actin to G-actin, as the amount of F-actin in the cells was unaltered after UVA exposure but rather due to direct breakage of the actin filaments. Ultraviolet B (297/302 nm) had no effect on the cellular distribution of microfilaments, not even at highly lethal fluences.