Amount of vascular development (veininess) is an important quality factor for processing wholepack tomatoes. The influences of nutrient and soil moisture stress on the amount of vascular development in `Chico III', `Dorchester', and `Roma' tomato fruit were studied. Fruit subjected to nutrient stress showed the highest amount of veininess. Fruit exposed to moisture stress after initial fruit set did not differ from controls in amount of veininess. Amount of vascularization did not differ among cultivars. A method for quantifying veininess was developed and compared with a traditional subjective rating scale. There was a high correlation (r2 = 0.77) between the subjective rating and quantitative measurement of veininess.
Tomato spotted wilt virus (TSWV) and Phytophthora infestans (late blight) in tomato (Solanum lycopersicum) have a worldwide distribution and are known to cause substantial disease damage. Sw-5 (derived from S. peruvianum) and Ph-3 (derived from S. pimpinellifolium) are, respectively, TSWV and late blight resistance genes. These two genes are linked (within 5 cM on several maps) in repulsion phase near the telomere of the long arm on chromosome 9. The tomato lines NC592 (Ph-3) and NC946 (Sw-5) were crossed to develop an F2 population and subsequent inbred generations. Marker-assisted selection (MAS) using three polymerase chain reaction-based codominant markers (TG328, TG591, and SCAR421) was used in F2 progeny with the goal of selecting for homozygous coupling-phase recombinant lines. From 1152 F2 plants, 11 were identified with potential recombination events between Ph-3 and Sw-5; of those, three were male sterile (ms-10). F3 progeny were generated from the remaining eight F2 recombinants, and resistance to both pathogens, or Ph-3 and Sw-5 in coupling phase, was confirmed in three of those. Recombination was suppressed fivefold in our F2 population to 1.11 cM between genes when compared with published maps of the same region. However, MAS was an efficient tool for selecting the desirable recombination events for these two pathogen resistance genes.