Microsatellite and Mitochondrial Data Provide Evidence for a Single Major Introduction for the Neartic Leafhopper Scaphoideus titanus in Europe

Scaphoideus titanus, a leafhopper native to North America and invasive in Europe, is the vector of the Flavescence dorée phytoplasma, the causal agent of the most important form of grapevine yellows in European vineyards. We studied 10 polymorphic microsatellite loci and a 623 bp fragment of the mitochondrial cytochrome oxidase II gene in native S. titanus from north-eastern America and introduced European populations, to elucidate the colonization scenario. Consistent with their recent history, invasive European populations were less genetically diverse than American populations for both types of markers, suggesting a recent bottleneck. Significant isolation by distance was detected between American populations but not between European populations. None of the European mitochondrial haplotypes was found in the American vineyards, from which they are assumed to have originated. The precise source of the invasive S. titanus populations therefore remains unclear. Nevertheless, the high heterozygosity of North-East American populations (which contained 92% of the observed alleles) suggests that this region is part of the native range of S. titanus. Clustering population genetics analyses with microsatellite and mitochondrial data suggested that European populations originated from a single introduction event. Most of the introduced populations clustered with populations from Long Island, the Atlantic Coast winegrowing region in which Vitis aestivalis occurs

The effect of age-related lens yellowing on Farnsworth-Munsell 100 hue error score

Purpose:  To investigate the effects of real and simulated age-related changes in crystalline lens yellowing on Farnsworth–Munsell (FM) 100 hue performance. Methods:  FM 100 hue total and partial error scores (PES) were measured in a group of younger (n = 10, mean age = 22.2 ± 2.65 years) and a group of older (n = 10, mean age = 54.5 ± 2.64 years) normal observers along with psychophysical estimates of crystalline lens optical density and pupil size. Three younger observers underwent repeated FM 100 hue testing under a variety of simulated age-related lens yellowing conditions, using filters with well-defined transmittance properties which attempted to mimic the real age-related lens yellowing changes of the older group. Results:  FM 100 hue total and PES were significantly higher in the older age group compared with the younger group (p < 0.01). Lens density measures were significantly higher in the older age group compared with the young group (p < 0.01), but showed less scatter than individual FM 100 hue error scores. Simulated lens yellowing in the three younger observers, equivalent to the level of that of the older observers, did not affect any of their FM 100 hue total or PES. Conclusions:  Simulation of age-related lens yellowing in younger observers has little effect on FM 100 hue error score. A variety of other factors such as pupil size, background illuminaton level, iris colour and macular pigment density may contribute to the age-related increase in FM 100 hue scores

How does the short-wavelength-sensitive contrast sensitivity function for detection and resolution change with age in the periphery?

AbstractTo determine the age-related change in the peripheral short-wavelength-sensitive (SWS) grating contrast sensitivity function (CSF), cut-off spatial frequency (acuity) and contrast sensitivity for both a detection and resolution task were measured at 8° eccentricity under conditions of SWS-cone isolation for 51 subjects (19–72 years). The acuity for both the detection and resolution task declined with age, the detection acuity being significantly higher than the resolution acuity at all ages (p<.01). The CSF for both detection and resolution shifted towards lower spatial frequencies with increasing age. The contrast sensitivity for detection remained higher than that for resolution for all ages at the highest spatial frequencies. The age-related loss in the SWS resolution CSF at high spatial frequency probably reflects a loss occurring at the ganglion cells level