References
- Science v.251 Free radicals within the Antarctic vortex: the role of CFCs in Antarctic ozone loss Anderson JG;DW Toohey;WH Brune https://doi.org/10.1126/science.251.4989.39
- J. Photochem. Photobiol. B. Biol. v.15 Photodamage to photosystem II-primary and secondary events Andersson B;AH Salter;I Virgin;I Vass;S Styring https://doi.org/10.1016/1011-1344(92)87003-R
- J. Exp. Mar. Biol. Ecol. v.194 Effects of ultraviolet (UV) radiation on microalgae-invertebrate symbiosis I. Response of the algal symbionts in culture and in hospite Banaszak AT;RK Trench https://doi.org/10.1016/0022-0981(95)00073-9
- J. Mar. Biol. Ass. v.31 Ecological and non-environmental constitutional resistence of the protoplasm of marine algae Biebl R. https://doi.org/10.1017/S0025315400053017
- Mar. Biol. v.131 UV-radiation can affect depth-zonation of Antarctic macroalgae Bischof K;D Hanelt;C Wiencke https://doi.org/10.1007/s002270050351
- Photochem. Photobiol. v.58 In vivo analysis of slow chlorophyll flurophyll fluorescence induction kinetics in algae: progress, problems and perspectives Buchel C;C Wihelm https://doi.org/10.1111/j.1751-1097.1993.tb04915.x
- Mar. Biol. v.130 Mycosporine-like amino acids: possible protection in eggs of the sea hare Aplysia dactylomela Carefoot TH;M Harris;BE Taylor;D Donovan;D Karentz https://doi.org/10.1007/s002270050259
- Antarctica. Kor. J. Phycol. v.9 Macroalgal vegetation of Maxwell Bay in King George Island Chung H;YS Oh;IK Lee;DS Kim
- Antarctica. Phycologia v.31 A year-round ecophysiological study of Himanthothallus grandifolius (Desmarestials, Phaeophyta) at Signy Island Drew EA;RM Hastings https://doi.org/10.2216/i0031-8884-31-3-4-262.1
- J. Exp. Mar. Biol. Ecol. v.104 Bathymetric adaptations of the reef-building corals at Davies Reef, Great Barrier Reef, Australia. III. UV-B absorbing compounds Dunlap WC;BE Chalker;JK Oliver https://doi.org/10.1016/0022-0981(86)90108-5
- Antact. J. U.S. v.30 UV-absorbing compounds in natural assemblages of Antarctic phytoplankton Dunlap WC;GA Rae;EW Helbling;VE Villafane;O Holm Hansen
- Phytochemistry v.26 Biosynthesis of mycosporine: mycosporine glutaminol in Trichothecium roseum Favre Bonvin J;J Bernillon;N Salin;N Arpin https://doi.org/10.1016/S0031-9422(00)83866-2
- Eur. J. Phycol. v.32 The changing irradiance environment: consequences for marine macrophyte physiology, productivity and ecology Franklin LA;R Forster
- Science v.241 Ultraviolet radiation levels during the Antarctic spring Frederick JE;HE Snell https://doi.org/10.1126/science.241.4864.438
- In Progress in Phycological Research v.9 Risks of enhanced solar ultraviolet radiation for aquatic ecosystems Hader DP;Round FE (ed.);DJ Chapman (ed.)
- Bot. Acta. v.109 Photosynthetic fluorescence induction and oxygen production in corallinacean algae measured on site Hader DP;H Hermann;J Schafer;R Santas https://doi.org/10.1111/j.1438-8677.1996.tb00575.x
- Ocean Polar Res. v.23 Effects of artificial UV-B and solar radiation on four species of Antarctic rhodophytes Han T;S J Park;M Lee;Y S Han;S H Kang;S Lee
- Scientia Mar. v.60 Photoinhibition of photosynthesis in marine macroalgae Hanelt D
- Mar. Biol. v.131 Capability of dynamic photoinhibition in Arctic macroalgae is related to their depth distribution Hanelt D https://doi.org/10.1007/s002270050329
- Bot. Acta. v.105 Photoinhibition of photosynthesis and its recovery in red algae Hanelt D;K Hupperts;W Nultsch https://doi.org/10.1111/j.1438-8677.1992.tb00299.x
- Mar. Ecol. Prog. Ser. v.149 Effects of high light stress on photosynthesis of polar macroalgae in relation to depth distribution Hanelt D;B Melchersmann;C Wiencke;W Nultsch https://doi.org/10.3354/meps149255
- Bull. Mar. Sci. v.32 Solar ultraviolet photobiology of the reef coral Pocillopora damiticornis and symbiotic zooxanthellae Jokiel PL;RH York
- Phycologia v.26 Seasonal growth and photoinhibition in Plocamium cartigineum (Rhodophyta) off the Isle of Man Kain JM https://doi.org/10.2216/i0031-8884-26-1-88.1
- Antarctic J. U.S. v.24 Report on studies related to the ecological implications of ozone depletion on the Antarctic environment Karentz D
- Antarctic Research Series v.62 Ultraviolet tolerance mechanisms in Antarctic marine organisms. In Ultraviolet radiation in Antarctica: measurements and biological effects Karentz D.;Weiler CS (ed.);PA Penhale (ed.) https://doi.org/10.1029/AR062p0093
- Limnol. Oceanogr. v.35 Evaluation of biologically harmful ultraviolet radiation in Antarctica with a biological dosimeter designed for aquatic environments Karentz D;LH Lutze https://doi.org/10.4319/lo.1990.35.3.0549
- Mar. Biol. v.108 Survey of mycosporine-like amino acid compounds in Antarctic marine organisms: potential protection from ultraviolet exposure Karentz D;FS McEuen;MC Land;WC Dunlap https://doi.org/10.1007/BF01313484
- Bot. Mar. v.41 An inventory of UV absorbing mycosporine like amino acids in macroal gae from polar to warm temperate regions Karsten U;T Sawall;D Hanelt;K Bischof;FL Figueroa;A Flores Moya;C Wiencke https://doi.org/10.1515/botm.1998.41.1-6.443
- Ann. Rev. Pl. Physiol. Pl. Mol. Biol. v.42 Chlorophyll fluorescence and photosynthesis: the basics Krause GH;E Weis https://doi.org/10.1146/annurev.pp.42.060191.001525
- Photosynthesis Res. v.36 The effect of UV-B radiation on photosynthetic and respiration of phytoplankton, benthic macroalgae and seagrasses Larkum AWD;WF Wood https://doi.org/10.1007/BF00018071
- Mar. Biol. v.109 UV-B protecting compounds in the marine alga Phaeocystis pouchetii from Antarctica Marchant HJ;AT Davidson;GJ Kelly https://doi.org/10.1007/BF01313504
-
Plant Cell Environ.
v.18
Evaluation of the role of damage to photosystem II in the inhibition of CO
$_2$ asimilation in pea leaves on exposure to UV-B radiation Nogues S;NR Baker https://doi.org/10.1111/j.1365-3040.1995.tb00581.x - Mar. Biol. v.80 Responses of Ecklonia radiata (Laminariales) to light at 15℃ with reference to the field light budget at Goat Island Bay Novaczek I https://doi.org/10.1007/BF00392821
- In Photoinhibition of photosynthesis, from the molecular mechanisms to the field What is photoinhibition? Some insights from comparisons of shade and sun plants Osmond CB;Baker NR (ed.);NR Bowyer (ed.)
- Aqua. Bot. v.45 UV-absorbing pigment, photosynthesis and UV exposure in Antarctica: comparison of terrestrial and marine algae Post A;AWD Larkum https://doi.org/10.1016/0304-3770(93)90023-P
- Mar. Biol. v.122 Depth dependent responses to solar ultraviolet radiation and oxidative stress in the zooxanthellate coral Acropora microphtalma Shick JM;MP Lesser;WC Dunlap;WR Stochaj;BE Chalker;Wu Won J https://doi.org/10.1007/BF00349276
- Bot. Mar. v.17 Distribution of a 334 UV-absorbing-substance in algae, with special regard of its possible physiological roles Sivalingam PM;T Ikawa;Y Yokohama;K Nisizawa https://doi.org/10.1515/botm.1974.17.1.23
- Photochem. Photobiol. v.29 Penetration of UVB and biologically effective dose-rates in natural waters Smith R;K Baker https://doi.org/10.1111/j.1751-1097.1979.tb07054.x
- Polar Biol. v.10 Seasonality of brown algae from Antarctica along term culture study under fluctuating Antarctic daylengths Wiencke C https://doi.org/10.1007/BF00239370
- Mar. Ecol. Prog. Ser. v.54 Temperature requirements for growth and temperature tolerance of macroalgae endemic to the Antarctic region Wiencke C;I tom Dieck https://doi.org/10.3354/meps054189
- Mar. Ecol. Prog. Ser. v.59 Temperature requirements for growth and survival of macroalgae from Antarctica and Southern Chile Wiencke C;I tom Dieck https://doi.org/10.3354/meps059157
- Mar. Biol. v.96 Effect of solar ultra violet radiation on the kelp Ecklonia radiata Wood WF https://doi.org/10.1007/BF00394848
- Aquat. Bot. v.33 Photoadaptive responses of the tropical red alga Echeuma striatum Schmitz (Gigartinales) to ultra-violet radiation Wood WF https://doi.org/10.1016/0304-3770(89)90019-3