Over recent geological time the Antarctic marine system has been a relatively low ultraviolet radiation (UV-R) environment because of its polar location, high atmospheric ozone concentrations, and extensive seasonal covering by relatively opaque, and highly reflective, sea ice. Recent increases in ultraviolet-B radiation (280-315·nm) due to stratospheric ozone depletion have highlighted the susceptibility of marine ecosystems to this important abiotic factor (Smith et al., 1992;Karentz, 1994;Smith and Cullen, 1995). The occurrence of the spring ozone hole coincides with the development of embryos of many Antarctic marine invertebrates that may be susceptible to the effects of UV-R because of their small size, lack of a protective tegument, and high rate of cell division (Johnsen and Widder, 2001). Antarctic embryos may be especially vulnerable because they have unique physiological adaptations to survive the cold, food-poor Antarctic waters (cf. Marsh et al., 2001).Our recent observations confirm that Antarctic marine larvae are very sensitive to UV-R (Lesser et al., 2004). Echinoid embryos exposed to ambient UV-R under annual Antarctic sea ice (a low UV-R environment with irradiances р1% of surface irradiances), exhibited significantly higher rates of mortality, abnormal development (Ϸ30-50%), and DNA damage than embryos exposed concurrently but under a UV-R filter. Biological weighting functions for DNA damage and survival To determine if an Antarctic species repairs DNA at rates equivalent to warmer water equivalents, we examined repair of UV-damaged DNA in echinoid embryos and larvae. DNA repair by photoreactivation was compared in three species Sterechinus neumayeri (Antarctica), Evechinus chloroticus (New Zealand) and Diadema setosum (Tropical Australia) spanning a latitudinal gradient from polar (77.86°S) to tropical (19.25°S) environments. We compared rates of photoreactivation as a function of ambient and experimental temperature in all three species, and rates of photoreactivation as a function of embryonic developmental stage in Sterechinus. DNA damage was quantified from cyclobutane pyrimidine dimer (CPD) concentrations and rates of abnormal embryonic development. This study established that in the three species and in three developmental stages of Sterechinus, photoreactivation was the primary means of removing CPDs, was effective in repairing all CPDs in less than 24·h, and promoted significantly higher rates of normal development in UV-exposed embryos. CPD photorepair rate constant (k) in echinoid embryos ranged from 0.33 to 1.25·h -1 , equating to a time to 50% repair of between 0.6 and 2.1·h and time to 90%repair between 3.6 and 13.6·h. We observed that experimental temperature influenced photoreactivation rate. In Diadema plutei, the photoreactivation rate constant increased from k=0.58·h -1 to 1.25·h -1 , with a Q 10 =2.15 between 22°C and 32°C. When compared among the three species across experimental temperatures (-1.9 to 32°C), photoreactivation rates vary with a Q 10 =1.39. Photoreactivati...