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SUMMARYUltraviolet (UV) vision plays an important role in interspecific and intraspecific communication in many animals. However, UV vision and its adaptive significance have been investigated in only approximately 1% of more than 5000 species of jumping spiders (Araneae: Salticidae), renowned for their unique, complex eyes that support exceptional spatial acuity and visually based behaviour. To appreciate the adaptive significance of UV vision, it is important to establish whether salticids can perceive UV and whether the perception of UV varies with ecological factors such as light environment. In this study, we measured the UV-transmission properties of the principal-eye corneas of 128 salticid species. We found that the corneas of all measured species were able to transmit UV light, making the perception of UV possible. Three classes of corneal spectral transmission curves were identified; the majority of species had a Class II curve with a less-steep slope and a gradual onset of the transmission cut-off; all the remaining species had a Class I curve with a very steep slope and a sharp cut-off except for one species that had a Class III curve with an intermediate step, which appeared as a shoulder on the descending part of the transmission curve. The T50 cut-off transmission values (the wavelength at which 50% of the maximum transmission is reached) in salticid corneas vary with species and light habitat. The corneas of species inhabiting open bush had a higher relative transmission at short wavelengths in the UV than forest species. This is the first investigation of corneal transmission in spiders and suggests that UV perception is widespread in salticids.

Fluorescence imaging with one-nanometer accuracy (FIONA) is a simple but useful technique for localizing single fluorophores with nanometer precision in the x-y plane. Here a summary of the FIONA technique is reported and examples of research that have been performed using FIONA are briefly described. First, how to set up the required equipment for FIONA experiments, i.e., a total internal reflection fluorescence microscopy (TIRFM), with details on aligning the optics, is described. Then how to carry out a simple FIONA experiment on localizing immobilized Cy3-DNA single molecules using appropriate protocols, followed by the use of FIONA to measure the 36 nm step size of a single truncated myosin Va motor labeled with a quantum dot, is illustrated. Lastly, recent effort to extend the application of FIONA to thick samples is reported. It is shown that, using a water immersion objective and quantum dots soaked deep in sol-gels and rabbit eye corneas (>200 µm), localization precision of 2-3 nm can be achieved.